This revised, and very large, aphid genera page is a concise draft summary of the biology & characteristics of all (530+) extant genera worldwide.
When using this list to identify aphids please remember that, owing to species introductions, the regions indicated are only a guide.
Alternate between galls on spruce (Picea spp.) & other conifers (Abies, Larix, Tsuga, Pseudotsuga) but not pine (Pinus spp.) though all are Pinaceae. Some remain on one or the other. Complete life cycle of host alternating Adelges takes two years.
Often identified by shape & colour of spruce gall. Apterae are medium-sized, generally brownish, & often covered in flocculent wax. Differ morphologically from 'true aphids' (Aphididae) in having fewer & shorter antennal segments, reduced wing venation of forewing of alate, often a highly glandular body surface, no siphunculi or cauda, & in all female forms being oviparous. Differ from Pineus by having five pairs of abdominal spiracles.
Host alternate between galls on spruce (Picea spp.) & pine (Pinus spp.) (both Pinaceae). Some remain on one host. Life cycle of host alternating Pineus takes two years. Galls usually on shoot tips, less compact than those of Adelges.
Apterae on secondary hosts are pear-shaped or globular, & generally secrete white wax-wool. Antennal tubercle not developed. Antenna in aptera 3-segmented, with third segment usually with primary rhinarium apically and a rhinarium medially, with secondary rhinaria absent; sometimes whole antenna reduced to small papilla. Antennae in alatae 5-segmented, with segments III-V usually with a large membranous rhinarium. Rostrum 4-segmented; apical segment broadly rounded. Spiracles on abdomen not operculate, with 4 present on each side of abdomen. Siphunculus absent. Cauda tiny, evident only as arc-shaped sclerite. Footit & Richards (1993)
On laurels (Lauraceae). Several species ant attended. Oviparae & males are both alate, & may be found at almost any time of year.
Apterae mostly yellowish or brown, some species dusted with white wax. Body with many long fine hairs. Ocular tubercles very small, especially in apterae. Antennal tubercles absent. Antennae covered with hairs, with terminal process shorter than base of antennal segment VI. Siphunculi well developed in females, on broad hairy cones; males lack siphunculi. Cauda very short, rounded. Tarsi normal. Formerly thought closely related to Anoecia, now in separate subfamily. Takahashi (1921)
Some species host alternate between dogwood (Cornus, Cornaceae) & roots of grasses (Poaceae). Others live year round on roots of grasses or sedges (Cyperaceae). While on grass roots they are ant attended.
Apterae are medium-sized, greenish-grey or grey in colour, with sclerotic dorsal abdominal plate. Antennae rather short, usually 6-segmented; terminal process short. Apterae usually have few secondary rhinaria; alatae have many all over antennal segments. Apterae usually have multifaceted eyes, fundatrices & immatures only have triommatidia. Hairs on body & appendages numerous. Alate sexuparae have characteristic dark dorsal abdominal patch & large black pterostigmal spot on forewing. Siphunculi are rather large round pores raised on shallow cones, surrounded by hairs. Cauda broadly rounded. Apterae of subgenus Paranoecia lack dorsal sclerotization, only have triommatidia as eyes even when adult. Blackman et al. (2019)
Krikoanoecia is still listed as a valid genus by Favret, but Blackman considered it "based on a vagrant sexupara of Eriosoma ulmi or a related species," hence a synonym of Eriosoma.
Only species, Aleurosiphon smilacifoliae, feeds on main veins & leaf undersides of Smilax china.
Body much covered with wax powder. Wings clouded along veins, unlike Aphis spp. Upper pair of apical primary hairs of second hind tarsal segment much longer than other primary hairs. Abdomen with 4 dorsal (spinal & pleural) hairs on each of abdominal segments I-VI. Alatae are without marginal sclerites on segments I-V. Marginal tubercles of abdominal segment VII below level of spiracles (like Aphis) in fundatrigenia, but at that level just behind spiracles (like Melanaphis) in fundatrix. Takahashi (1966)
Most spp. live on shrubs or herbs, relatively few on trees; rarely on grasses (Poaceae), never on sedges (Cyperaceae). Some host alternate between woody perennials & herbaceous annuals. Usually live on young foliage, often distort leaves. Some spp. live on stem base, or on roots. Many ant attended. Many are important crop pests. Genus includes several subgenera, namely Bursaphis, Iowana, Maculaphis, Pseudoprotaphis, Toxoptera & Zyxaphis
Very small to rather large aphids, often greenish, sometimes yellow, brown, reddish, or black. Body broadly oval, never elongate. Antennae usually 6-segmented; terminal process 1-5 x base of segment VI. Dorsum membranous with variable dark sclerotic markings. Siphunculi more-or-less cylindrical or tapering, never distinctly swollen. Cauda usually more-or-less elongate. Legs variably pigmented, but rarely all dark. Stroyan (1984)
Brachyunguis50 spp. S Europe, N Africa, Asia, America
On amaranth (Amaranthaceae) & some other families. Live in arid regions.
Grey or green, often coated with mealy wax. Head devoid of frontal tubercles. Antennae short. Terminal process very short, usually shorter than antennal segment VI base. Clypeus often globose. Apical rostral segment usually shorter than second segment of hind tarsus. Little body sclerotization. Siphunculi very short, subcylindrical or conical. Cauda conical, triangular, or finger-shaped. Related to Aphis spp. Das (1918)
Monoecious holocyclic on wild buckwheat (Eriogonum, Polygonaceae).
Medium-sized blackish aphids with dorsal cuticle reticulated; often have white wax markings. Antennae short, with very short terminal process. Apterae often with secondary rhinaria on antennal segments III or III-V. Apical rostral segment long & narrow. Marginal tubercles present on tergites I & VII. Siphunculi short, dark, less than 3 x longer than width at base. Cauda short, broadly triangular. Differ from Aphis in having shorter terminal process, short siphunculi, & very short broad cauda. Gillette & Palmer (1929)
Casimira canberrae, feeds on young leaves of willowherb (Epilobium, Onagraceae). Genus endemic to Australasia, at risk of extinction due to competition from invasive Aphis oenotherae.
Apterae are small to medium sized, black & wax-powdered. Antennae 5 or 6-segmented, about 0.5 x body, with terminal process 3.3-3.7 x base antennal segment VI. Antennal hairs short. Rostrum reaches just past mesocoxae. All first tarsal segments bear only two hairs with no medial sense peg. Alatae have once-branched media. Marginal tubercles present on prothorax & abdominal segment I, but absent on segment VII. Siphunculi short, narrowing abruptly from broad base to apex. Cauda large & black, with 4-6 hairs. Differ from Aphis re hairs on first tarsal segments, marginal tubercles & wing venation. Eastop (1961)Eastop, (1966)et al. (1971)
Chomaphis1 sp. Russia, Ukraine, Kazakhstan, N Italy
Only species is Chomaphis mira which feed on roots of butterbur (Petasites), coltsfoot (Tussilago), burdock (Arctium) (all Asteraceae).
Medium sized aphid, which differs from Aphis in having first tarsal segments bearing 4,4,3 hairs, a very short cauda, long siphunculi with small hairs, & very large marginal tubercles.
Eastopiella1 sp. Botswana, Tanzania, Zimbabwe, S Africa
Only species, Eastopiella evansi, feeds on Vernonia glabra & other Asteraceae at base of stem with ant attendance.
Apterae medium sized, dull, mottled greenish or brownish red. Frons strongly convex with ocellus situated in center of frons. Antennae six-segmented, segment III with 1-5 secondary rhinaria. Rostrum reaches the hind coxae. Apical rostral segment long, stiletto-shaped. First segment of tarsus with 3,3,2 hairs. Marginal tubercles developed on the prothorax, tergites I & VII. Siphunculi dark, subcylindrical, 0.65-0.75 x cauda. Cauda is pale, triangular-conic, with basal constriction, & 12-18 hairs. Genus differs from other genera of subtribe Aphidina by presence of ocellus in aptera, but recent studies indicate should perhaps remain in Protaphis.Kadyrbekov (2001)
Feed on joint-pine (Ephedra, Ephedraceae) & saxual (Haloxylon, Amaranthaceae).
Apterae are medium sized, blackish green or brown, usually with transverse white wax dorsal stripes. Frontal tubercles developed, frons shallowly W-shaped. Antennae usually 6-segmented, with terminal process up to 2.6 x longer than segment base. Rostrum rostrate with microtrichia covering surface. First tarsal segments have 3,3,3 hairs. Siphunculi short to long, cylindrical. Cauda usually short, tongue shaped with 5-8 short hairs on apex. Genital plate tranversely oval. Related to Aphis, but differs in rostrum with microtrichia, short cauda and first tarsal chaetotaxy. Hille Ris Lambers (1959)Zhang & Qiao (2013)
Only species, Misturaphis shiloensis, feeds on field wormwood (Artemisia campestris ssp. caudata, Asteraceae).
Rather small species, greyish green to pale green. Antennal tubercles not produced. Antennae 5-segmented in both apterae & alatae; secondary rhinaria absent in aptera. Hairs on head & antennae comparatively long & spear-shaped. Rostrum reaches hind coxae. First tarsal segments each with 2 hairs. Marginal tubercles absent on abdominal tergites I & VII. Robinson (1967)
Only species, Nevadaphis sampsoni, lives in colonies on roots of sagebrush (Seriphidium tridentata, Asteraceae), sometimes ant attended. No evidence of sexual or alate forms.
A medium sized species, dirty yellow to reddish brown, often mottled. Antennae 6-segmented, shorter than body, terminal process about as long or longer than base of segment VI. Ocular tubercle large. Rostrum shorter than body. Siphunculi very short, cylindrical, with flange. Cauda apparently ovate, with long hairs, longer than siphunculi. Distinguished from Aphis by greatly reduced siphunculi & cauda. Drews (1941)
Paradoxaphis aristoteliae feeds on leaves of wineberry (Aristotelia serrata, Elaeocarpaceae); Paradoxaphis plagianthi feeds on ribbonwood (Plagianthus regius, Malvaceae).
Apterae are medium sized, brown or brown, with a green to dark brown longitudinal stripe. Antennal tubercles moderately developed. Antennae 6-segmented, as long as or longer than body; apterae & alatae both without secondary rhinaria. Rostrum extends to hind coxae. First tarsal segments have 3,3,2 hairs. Spiracles on segments I & II widely separated. Differ from Aphis in having no marginal tubercles on tergite VII & often tergite I. Siphunculi strongly developed, tapering. Cauda pointed & finger shaped. Sunde. 1988 [1987]
Pehuenchaphis agilissima feeds on roots of ragwort (Senecio, Asteraceae); thought to be monoecious holocyclic.
Apterae medium-sized, dark green to brown, sometimes wax-dusted. Triommatidium not easily distinguished. Antennae & legs relatively long, terminal process longer than base of segment VI. Numerous long antennal hairs. Secondary rhinaria present in apterous forms. Apical rostral segment long. Marginal tubercles on abdominal tergite I, frequently on II-VI, but may be absent on VII & prothorax. Siphunculi short, sited on anterior of segment VI or absent. Cauda blunt & relatively wide. Differ from Aphis in having reduced siphunculi, & reduced triommatidia. Mier-Durante & Nieto Nafria (2003)
Protaphis42 spp. Europe, Central Asia, Africa, N America
Protaphis spp. feed at stem base & roots of Asteraceae, Fabaceae, Campanulaceae, Rutaceae. Usually attended by ants.
Apterae small to medium sized, with short appendages & other morphological features adapted to their mode of life. Antennae shorter than body, with short terminal process; secondary rhinaria on segment III (and rarely IV) in apterae & alatae. Rostrum long, with apical rostral segment blunt, not stiletto-shaped. Dorsum frequently with well developed sclerotic pattern, but postsiphuncular sclerites absent. Siphunculi dark, relatively short & conic, similar in length to triangular cauda which has 10-25 hairs. Heie (1986)
Ryoichitakahashia prunifoltae feeds on Japanese winterberry (Ilex serrata, Aquifoliaceae). Forms dense colonies on stems.
Apterae are medium sized, broad-bodied, dull reddish-black with banded antennae, & jet black siphunculi. Antennal tubercles very strongly diverging. Antennae about as long as body, with long terminal process. Apterae have secondary rhinaria on segment III, & frequently IV. Rostrum reaches middle of hind coxae, with apical rostral segment thick & blunt. Dorsal hairs long, fine & wavy with marginal hairs most numerous. Siphunculi tapering, about 0.2 x body length, with hardly developed flange. Cauda short, bluntly conical to rounded, with 18-24 long hairs. Differs from Aphis in having numerous marginal hairs, & secondary rhinaria in apterae. Hille Ris Lambers (1965)
Sanbornia juniperi are monoecious holocyclic on juniper (Juniperus, Cupressaceae). Males are alate.
Apterae are rather small, coloured green, & covered with flaky wax. Head without prominent antennal tubercles. Aptera has 4-segmented antennae, & prominent mushroom-like projection on the vertex. Abdomen of aptera has unusual humpback-shape with tubercle at highest point; marginal abdominal tubercles are absent. First tarsal segments minute, without hairs. Siphunculi reduced to pores; cauda elongate & tapering. Alate has 5-segmented antennae, forewings with media once branched. Baker (1920)
Seneciobium balachowskyi are monoecious holocyclic on stems & flowers of Jacobaea (= Senecio) adonidifolia (Asteraceae).
Apterae are medium sized, greenish to black, with waxy bloom, & appendages all dark, including cauda. Forehead bears distinct median & antennal tubercles. Antennae are 0.50-0.67 x body length, with short terminal process. Secondary rhinaria always present on antennal segments III & IV. Rostrum reaches posterior coxae. Siphunculi complete absent, but in their usual location were cuticular invaginations, usually pigmented. Cauda elongated, rounded at tip. Blackman noted the resemblance to other Senecio-feeding Aphis, & suggests its separate generic status may not be warranted, despite lack of siphunculi. Remaudiere (1954).
Siphonatrophia2 spp. W USA, Mexico, Honduras, Costa Rica, Argentina, s Europe, Tunisia, Japan
Siphonatrophia species are monoecious holocyclic on cypress (Cupressaceae).
Siphonatrophia cupressi is a rather small, pale blue-green aphid, with body strongly domed dorsally & flattened against leaf ventrally. Antennae with 5-6 segments, & terminal process about equal to base of segment VI. Rostrum reaches middle coxae. Abdomen without marginal tubercles. Siphuncular pores on very small, shallow cones. Cauda triangular, with more than 10 hairs. Other species recognised is Siphonatrophia aetherelaca.Lumbierres (2015)
Only species, Szelegiewicziella chamaerhodi, feeds on Chamaerhodos erecta (Rosaceae).
Rather small aphids, green with greyish wax exudation. Antennal tubercles not developed. Apterae & alatae both have 4-segmented antennae, with long terminal process. Secondary rhinaria only present in alatae. First tarsal segments have 3,3,2 or 3,2,2 hairs. Apterae have smooth dorsal sclerotic shield, with stout dorsal hairs. Spiracular pores widely kidney-shaped. Marginal tubercles on abdominal segments I & VII, as in Aphis.Holman (1974)
Toxopterina feed on roots of yarrow (Achillea, Asteraceae) living in small dense colonies.
Apterae are rather small dark green aphids, with dark siphunculi. Differentiated from Aphis by following characters: media of forewing usually with only 1 fork; terminal process rarely shorter than 4.5 x base antennal segment VI; cauda triangular.
Genus was accepted by Heie (1986) as a single species genus including only Toxopterina vandergooti. Blackman treated Toxopterina as a subgenus of Aphis, & now includes both Aphis (Toxopterina) achillearadicis & Aphis (Toxopterina) vandergooti. Favret treats Toxopterina as a genus, with Toxopterina vandergooti as the only species in the genus. Heie (1986)
Xerobion aphids feed on plants in the daisy family (Asteraceae), especially Anthemidae; also several plants in Chenopodiaceae.
Apterae mostly rather small, with dark siphunculi. Some species wax-coated, others without wax & almost shiny. Antennae short, 6-segmented, with short antennal terminal process, not longer than base of segment VI. Apterae without secondary rhinaria. Small marginal tubercles on prothorax, & abdominal segments I & VII. Hairs on body pointed. The siphunculi are short, volcano-shaped. Cauda is bluntly conical, equal to or longer than siphunculi. Characterised by short siphunculi. Nevsky (1929)
Asiphonaphis pruni feeds on cherry (Prunus, Rosaceae) (=primary host?), Asiphonaphis japonica feeds on sedge (Carex, Cyperaceae) (=secondary host?). Host of Asiphonaphis utahensis uncertain.
Medium sized, variable colour. Frontal tubercles weakly developed. Antenna
6-segmented; terminal process elongate; primary rhinarium with
ciliated margin, secondary rhinaria usually only present in alata on segments III & IV. Both alatae & apterae have prominent marginal tubercles on tergites I-VII. Completely lack siphunculi. Possibly related to Rhopalosiphum &/or Aphis.Asiphonaphis may not be valid genus. Wilson & Davis (1919)
Apterae medium sized, usually greenish. Head & dorsum strongly spinulose head, abdominal spinules not arranged in polygons as in Rhopalosiphum. Antennal tubercles absent. Antennae usually 5-segmented antennae, with rather long terminal process. Rhopalosiphum-like siphunculi, vasiform or slightly swollen. Cauda short & rounded, about 1.5 x its basal width, with only 4-5 hairs. Similarity to Rhopalosiphum probably due to morphological convergence of grass root feeders. Eastop (1958)
Hyalopterus3 spp. S Europe, N Africa, Central Asia, China, N America
Usually host alternate between plum (Prunus, Rosaceae) & reed grass (Phragmites, Poaceae). Not attended by ants. One species is important pest of plum trees.
Small to medium sized elongate aphids. Usually pale green mottled with darker green, on secondary host some are pink. Covered with white waxy meal. Antennae shorter than body, with terminal process 2.5-4.0 x base antennal segment VI. Rostrum hardly reaching middle coxae, with apical segment short & squat. Dorsal body cuticle wholly pale & membranous. Marginal tubercles may be present on pronotum & abdominal segments I-VII, but often missing on some segments. Siphunculi very short, more or less cylindrical, without any trace of flange. Cauda elongate, more or less finger-shaped, & longer than siphunculi. Stroyan (1984)
Hysteroneura1 sp. originally N American, now widespread in warmer regions.
In N America only species, Hysteroneura setariae, host alternates from pseudogalls on plum (Prunus, Rosaceae) to grasses (Poaceae), or rarely Cyperaceae or Palmaceae. In warmer countries often anholocyclic on Poaceae.
Apterae brown, with black siphunculi & pale cauda. Head without prominent antennal tubercles. Antennae of six segments; rather few subcircular sensoria present in alatae. Forewings with 3-branched media vein on forewing, & single cross vein on hind wing. Siphunculi somewhat tapering or subcylindrical. Anal plate rounded. Baker (1920)
Most species monoecious on grasses (Poaceae: Miscanthus or Arundinaria). Few spp. host alternate between Rosaceae & Poaceae. Can be serious pest of pears.
Small to medium-sized, elongate oval or pear-shaped aphids. Usually brown or blackish. Abdomen has dark dorsal markings. Dorsal cuticle sometimes with reticulation Siphunculi more or less cylindrical, shorter than cauda. Winged forms have dark forewing veins with media vein twice-branched. Closely related to Rhopalosiphum, but cauda with more than 11 hairs. Heie (1986)
Mordvilkoiella jacutensis is pale yellowish green. Thought to be related to Hyalopterus, but have short 5-segmented antennae, siphunculi reduced to pores & no marginal abdominal tubercles. May be closer to subgenus Holcaphis of Diuraphis.
Thought to host alternate between dogwoods (Cornaceae) & Pilea (Urticaceae) or Scutellaria (Lamiaceae).
Apterae medium sized with extensive wax secretion. Antennal & median frontal tubercles absent. In alate second fork of media vein in fore wing is very close to wing margin, & is sometimes absent. Number of hairs of first tarsal segments is usually 3,3,2. Abdominal marginal tubercles slender, about twice as long as wide. Siphunculi very small, inconspicuous, flangeless with narrow pores, & situated between tergites V & VI. Robinson. (1965)
Only species Pseudotoxoptera pyrisucta is thought by Blackman in AWP to be a synonym of Aphis eugeniae. Closely related to Aphis subgenus Toxoptera, but Pseudotoxoptera differs in having the vocal ridges [=stridulatory surface] on the ventral surface of the abdominal segments not very distinct. Also the siphunculi are about 1.9 x longer than the cerci (for Toxoptera up to 1.40 x), and the cauda has 9-11 hairs (for Toxoptera more than 16). Zhang, Qiao & Zhong (2009)
Rhopalosiphum17 spp. Europe, Middle East, Asia, Africa, N America.
Most Rhopalosiphum spp. host alternate between Prunus/Pyroidea & Poaceae/Cyperaceae; a few are monoecious on one or the other. May be ant attended. Genus includes several important cereal pests.
Small to medium-sized green or brownish aphids, oval to rather elongate in shape. Antennae usually 6-segmented, shorter than body; without secondary rhinaria in aptera. First tarsal segments have 3,3,2 hairs. Marginal tubercles present on prothorax, & segments I & VII (occasionally others). Siphunculi longer than cauda, with an apical expansion & strong flange. Cauda finger- or tongue-shaped. Winged forms have a dorsal abdominal pigmented pattern. Heie (1986)
Schizaphis46 spp. Europe, Middle East, Asia, Africa, N America.
Half of species live all year on grasses (Poaceae); most of the rest (subgenus Paraschizaphis) live on sedges (Cyperaceae) or cattails (Typhaceae); a few host alternate between pear (Pyrus) or apple (Malus) & Poaceae.
Apterae are small to medium sized, ovate to somewhat elongate in shape, coloured greenish-yellow, brown or black. Frons with distinct but rather low frontal tubercles. Antennae 5- or 6-segmented, shorter than body. Rostrum short, not reaching beyond middle coxae. Forewing of alate has median vein only once branched. Siphunculi cylindrical to slightly tapering. Cauda blunt finger shaped, from about half as long as, to slightly longer than, siphunculi. Heie (1986)
Little is known about this genus. Swirskiaphis polychaeta feeds on umbellifers (Apiaceae), especially giant fennels (Ferula), Prangos & Dorema.
Apterae are medium sized, colour unknown. Frons more or less straight. Antennae 6-segmented, with elongated terminal process. Without secondary rhinaria in aptera, present on segment III in alatae. Membranous abdominal dorsum with numerous very long, thick dorsal hairs on large dark sockets.
Ventrally placed marginal tubercles on abdominal tergites I & VII. Close to Aphis, but dorsal hairs distinctive. Blackman in AWP comments that second species in genus, Swirskiaphis bambuciepula, more likely a Melanaphis.Hille Ris Lambers (1966)
Small to medium sized aphids, mostly dark, but with one common pale species. Apterae have small sparse spinules on dorsum of head capsule, often arranged in curving rows. Antennal segment III is covered with imbrications, with rarely 1-2 secondary rhinaria. Number of hairs on first tarsal segments is 3,3,2. The pentagonal hexagonal reticulated pattern of the tergum is distinctive. Siphunculi cylindrical over most of length, slightly swollen toward tip, imbricated throughout, and with small flange. Cauda moderately long. Alate viviparae usually have pigmented cross-bands on the abdomen. Jensen & Stoetzel (1999)
Acaudella puchovi feeds on Atraphaxis buxifolia & Atraphaxis spinosa, both knotweeds (Polygonaceae), in large colonies on leaf undersides.
Apterae rather small, with egg-shaped body, coloured dark green. They are without antennal tubercles and antennae are 5-segmented; terminal process is short. Marginal tubercles absent or inconspicuous. Siphunculi are slightly curved, swollen almost over whole length, and with bases and apices constricted. Cauda is absent. Nevsky (1929)
Acaudinum feed on stem base & roots of centaury (Centaurea) species. They are attended by ants.
Apterae are medium-sized, dark brown to blackish aphids. Head lacks antennal or median tubercles. Antennae have long terminal process and both apterae & alatae have many secondary rhinaria. Siphunculi are long, tapering and dark with indistinct flange. Cauda very short, broad and rounded, bearing numerous hairs. Blackman et al. (2010)
Apterae have median frontal tubercle and antennal tubercles undeveloped. Body dorsum is smooth without sclerites. Cauda is characteristic - semicircular at basal part and strongly constricted to pointed finger-shaped at distal part, and special anal plate which the hind margin forward indent to two conical tubercles. Qiao & Xu (2023)
Feed on members of the daisy family (Asteraceae), especially goldenrod (Solidago) and fleabane (Erigeron).
Apterae rather small, yellowish, greenish or reddish, one species with black dorsal shield. No distinct frontal tubercles. Apterae have secondary rhinaria. First tarsal segments with 3,3,2 or 3,3,3 hairs. Capitate hairs present. Siphunculi are truncated, conical, quite smooth, with marked annular incision before well developed flange. Cauda more-or-less elongated and pointed. Resemble Brachycaudus helichrysi in general appearance, but distinguished by secondary rhinaria on aptera & capitate hairs. Hille Ris Lambers (1956)
Only species, Acutosiphon obliquoris, has been found on various different hosts, mainly heaths (Lyonia ovalifolia, Ericaceae) and sedges (Carex, Cyperus, Cyperaceae). May be host alternation between those two families.
Apterae medium sized, red-brown. Frons with low diverging antennal tubercles. Antennae 5-segmented, short, without secondary rhinaria. Rostrum stout, just reaching midcoxae; apical rostral segment blunt & thick. First tarsal segments bear 5,5,5, hairs. Tergum sclerotic, wrinkled, with polygonal pattern on spino-pleural areas of abdomen. Distinctive warty pitted siphunculi, broad at base, tapering sharply to apex, with opening obliquely placed. Cauda thumb-shaped with 2 pairs of hairs. Basu et al. (1970)
Feed on various dicots, particularly Fabaceae, Rosaceae, and Euphorbiaceae.
Rather large broadly spindle-shaped, short-haired aphids with long appendages, siphunculi and cauda. Usually green - sometimes brownish, pink, or yellow. Antennal tubercles well developed, with diverging inner sides. Median frontal tubercle is very small or absent. Antennae about as long as body or longer. Siphunculi are cylindrical or tapering with distinct flange. Cauda is tongue- or finger-shaped. Blackman et al. (2010)
Feed on knotweeds (Polygonaceae), one species has sexual phase on Enkianthus (Ericaceae).
Apterae are medium sized, often brightly coloured orange, yellow, green with black Phorodon-like projections on the antennal tubercles, but head not spiculose. Spiracular apertures on abdominal segments I-V remarkably small. Paired processes on tergite VII and larger median one on VIII. Cauda has characteristic knobbed shape. Alatae with numerous tuberculate secondary rhinaria, hypha-like projections associated with the rhinaria, & much thinner, clavate siphunculi. Blackman & Eastop (1982-)
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Allocotaphis3 spp. Austria, Russia, Iran, Kazakhstan, India, China
Allocotaphis quaestionis host alternates be0tween apple (Malus, Rosaceae) where they roll leaves in spring, and Senecio doronicum (Asteraceae).
Apterae are rather large, green with a waxy bloom. Dense fine hairs present on head, sides of body, & proximal segments of legs. Siphunculi very long, reaching 3.0 x the rather short cauda. Borner & Heinze (1957)
Alphitoaphis1 sp. USA (Minnesota, Nebraska, Illinois, Kansas)
Only species, Alphitoaphis lonicericola, feeds on honeysuckle (Lonicera, Caprifoliaceae) causing leaf-curl. Prefers tender leaves of terminal branches.
Apterae medium sized, yellowish brown or reddish purple, dusted with wax powder. Antennae 6-segmented; secondary rhinaria absent in aptera, numerous in alate. Body much rounded. Abdomen without tubercles. Siphunculi cylindrical of uniform thickness throughout. Cauda broad at base, tapering gradually to point. Anal plate rounded. Related to Hyadaphis, but with thinner siphunculi and hind wings of alata have only one oblique vein. Hottes (1926)
Only species, Amegosiphon platicaudum, feeds on barberry (Berberis, Berberidaceae).
Apterae are medium sized, rather elongate-bodied with long appendages. Colour is pale green to yellowish with irregular red spinal stripe. Antennal tubercles diverging, with barely noticeable median tubercle. Antennae 6-segmented, with 3-5 secondary rhinaria in aptera. Rostrum very short, reaching to base of middle coxae. Siphunculi are characteristic - short, slightly & uniformly swollen over most of length, narrowing at base and apex. Cauda lanceolate, without constriction. Narzikulov (1958)
Only species, Ammiaphis sii, feeds on sickleweed (Falcaria vulgaris, Apiaceae).
Apterae are medium sized. Frons almost straight, rough with flat warts and wrinkled. Antennae 6-segmented, just over 0.5 x body length, with terminal process about 2.5 x base of segment VI. Both alatae and apterae have secondary rhinaria on antennal segments III & IV, with none on basal third. Siphunculi quite long, about 2 x cauda, scaly, tapering, slightly swollen distally. Cauda is triangular to sword-shaped. Koch (1855)
Amphicercidus10 spp. E Asia, C Asia, India, N America
Most feed on Caprifolicaceae, one on Forsythia (Oleaceae), another on Stauntonia (Lardizabalaceae). Most feed on leaves or stems, but Amphicercidus pulverulens feeds on bark, at or below ground level.
Medium sized, apterae mostly green or brown, and covered to variable extent with wax. Frontal tubercles only partially developed. Both alate and apterous viviparae have numerous secondary rhinaria on antennal segment III. Forewing has media vein twice-forked. Siphunculi cylindrical, & transversely wrinkled. Cauda very short, broad and semilunar. Oestlund(1923)[1922]
About half of species feed on brambles (Rubus, Rosaceae), others on variety of plants including ferns.
Apterae medium-sized to large rather pale greenish aphids. Adult viviparae may be winged or wingless. Body elongate or oval, with long legs and antennae, latter longer than body. Antennal tubercles well developed, with inner margins nearly straight and distinctly divergent. First tarsal segments with 3 hairs. Siphunculi long, distinctly swollen on distal half, with clearly marked apical flange, and without regular reticulations. Cauda finger-shaped or triangular. Blackman (2010)
Only species, Amphorosiphon pulmonariae, feeds on undersides of leaves and petioles of lungworts (Pulmonaria, Boraginaceae); also sandworts (Eremogone) & campions (Silene), both in Caryophyllaceae.
Apterae rather large, green with black siphunculi & dark dorsal markings. Frontal tubercles well developed. Antennae very long & slender, with very long terminal process. Numerous secondary rhinaria present in both apterae & alatae. Rostrum very long & extraordinarily hairy. Abdominal tergum membranous, with large postsiphuncular sclerites & smaller antesiphuncular sclerites. Siphunculi blackish sclerotic, with basal 0.3 about cylindrical, remainder rather strongly swollen. Cauda rather long, with distinct constriction. Differ from Amphorophora in presence of ante- & postsiphuncular sclerites & long, very hairy rostrum. Hille Ris Lambers (1949)
Anaulacorthum2 spp. W Bengal, India & Hunnan, China
Hosts of aphids rather diverse - one species (A. fagopyri ) feeds on buckwheat (Fagopyrum cymosum, Polygonaceae) in India; other species (A. zhangjiajiense feeds on sowthistle (Sonchus oleraceus, Asteraceae) in China.
Apterae are medium sized, and pale brown or pale red. Genus characterized by having head spinulose, rather short antennal & dorsal abdominal hairs, slightly clavate siphunculi with distinct apical flange, and 4,4,4 hairs on first tarsal segments. Genus is close to Aulacorthum, but they have chaetotaxy of 3,3,3 hairs. Ghosh & Raychaudhuri (1972)
Anthracosiphon2 spp. Holarctic (N America, N Europe)
Both species feed on runners of cinquefoils (Potentilla, Rosaceae).
Apterae medium-sized. A. crystleae are reddish brown; A. hertae shiny black dorsally, with rosy hue ventrally. Both with black antennae and siphunculi. Frontal tubercles well developed. Antennae long with secondary rhinaria on segment III in both apterae & alatae. Extensive dark dorsal sclerotisation and spicules on venter of head. Siphunculi long, cylindrical with subapical reticulation & well developed flange. Cauda shortly triangular. Closely related to Macrosiphum, differences possibly due to different microhabitat. Hille Ris Lambers (1947)
Feeds on Indian gooseberry (Phyllanthus emblica, Phyllanthaceae).
Only species, Antimacrosiphum bullacaudatum is medium sized with dark siphunculi. Antennae 6-segmented, longer than body. Basal part of segment III in aptera bearing one small secondary rhinarium. Rostrum reaching mid-coxae. Number of hairs on first tarsal segment 5,5,5. Siphunculi long, barrel-shaped, with apical one eighth reticulated. Cauda knobbed, basal third distinctly constricted. Related to Macrosiphum, but differs in cauda & secondary rhinaria. Blackman comments very similar to Sitobion so may not justify separate generic status. Zhang (1998)
Fundatrices feed in spring in pseudogalls on pear (Pyrus, Rosaceae). Alate offspring migrate to roots of daisies (Asteraceae) and umbellifers (Apiaceae) where tented by ants.
Apterae medium sized, olive-green to brown. Without frontal tubercles. Both apterae & alatae have many secondary rhinaria on antennal segment III. First tarsal segments all have 3 hairs. Abdomen has rather flat round spinal and marginal tubercles on most tergites, with dark sclerotic markings. Siphunculi short, but longer than cauda, with closely-spaced rows of densely-packed spinules or nodules. Cauda short, semicircular with many hairs. Related to Dysaphis but distinguished by siphunculi, large flat tubercles & hairy cauda. Blackman (2010)
Only species Anuromyzus cotoneasteris feeds on undersides of curled leaves of Cotoneaster spp. (Rosaceae)
Apterae medium sized, very shiny dark brown. Related to Dysaphis, but differs in having extensive dorsal sclerotisation and different siphunculi and cauda. Blackman & Eastop (1982-)
Feed mainly at stem apices of Caryophyllaceae; some species feed on woody hosts, namely Prunus and Prinsepia (Rosaceae), which may function as primary hosts for host-alternation.
Apterae characterized by presence of pair of mesosternal mammariform processes. Other characters include frons w-shaped with antennal tubercles not much higher than the broad median tubercle, antennae no longer than body length, thorax and abdomen often with a dorsal pattern of sclerotization that is variable within & between species, and siphunculi usually with a distinct preapical incision and flange. Hille Ris Lambers (1956)
The one species Aphiduromyzus rosae feeds on rose (Rosa, Rosaceae).
Apterae rather large, dark green or brown, with dark dorsal pigmentation, pale siphunculi and blackish cauda. Both apterae and alatae have numerous secondary rhinaria on antennal segment III. Alatae have an extensive black dorsal abdominal patch. Close to Aphidura, but lacks mammiform process on mesothorax, has well defined marginal tubercles & many secondary rhinaria. Also close to Myzus. but has low antennal tubercles, many secondary rhinaria in aptera, unique sclerotization of body, & well defined marginal tubercles. Umarov & Ibraimova (1967)
One species, host alternates between snowberry (Symphoricarpos, Caprifoliaceae) & Koenigia(= Aconogonon)(Polygonaceae); other species monoecious on Symphoricarpos. Feeding by the aphids curls leaves.
Adult apterae of Aphthargelia have a mostly dark, sclerotized, and reticulated dorsum. Antennae 6-segmented, without secondary rhinaria, with long slender terminal process. Rostrum with apical segment subconical. There are marginal tubercles, often very large, on thoracic segments and abdominal segments II-VI. Siphunculi are dark pigmented, about as long as or shorter than cauda, with apical half or more usually clavate. Cauda triangular, with apex narrow, pigmented or pale, with 10-20 hairs. Foottit & Richards (1993)
One species, Artemisaphis artemisicola feeds on Artemisia & Seriphidium (Asteraceae).
Apterae are medium sized, shiny dark reddish wine-coloured. Antennal tubercles low. First antennal segment thickened, gibbous on inner surface. Siphunculi of medium length, imbricated, with few rows of reticulation at distal end. Anal plate with a ventral wartlike protuberance pointing chiefly downwards. Cauda short, distinctively-shaped. Another species, Artemisaphis longicauda, has been described by Zheng & Zhong (1981) in China, but they only gave Artemisaphis subgenus status within genus Obtusicauda, based on its longer cauda. Knowlton & Roberts (1947)
Aspidaphis2 spp. Europe, SW&C Asia, Pakistan, N America
One species Aspidaphis adjuvans feeds on Polygonum aviculare (Polygonaceae), the other, Aspidaphis porosiphon feeds on Festuca rubra (Poaceae).
Medium sized aphids, coloured greenish, yellowish or brownish. Characterised by having cowl-like backward projection of abdominal tergite VIII which obscures cauda in dorsal view. Antennae 5-segmented, short; in apterae without secondary rhinaria. First tarsal segments have 3,3,2 hairs. Dorsum sclerotic or granulate with very short hairs. Siphunculi either short, without flange, with aperture positioned laterally before tip, or reduced to pores. Blackman (2010)
Subgenus Aspidophorodon feed on Salix (Salicaceae) in E. Asia, and subgenus Eoessigia feed on Rosaceae in Asia and North America. One species in India host-alternates between Cotoneaster and Potentilla (both Rosaceae).
Apterae medium sized, and usually pale yellowish or greenish, sometimes waxy. The head of the aptera bears forward directed medial and lateral projections. Antennae are 4- or 5-segmented with terminal process 0.6-1.6 x base of antennal segment VI. Apterae without secondary rhinaria on antennal segment III. First tarsal segments with 3,3,3 hairs. Tergum sclerotic. Siphunculi have clavate ends with the aperture small and subapical. Cauda with basal and medial constrictions. There are spinal processes in subgenus Eoessigia.Verma (1967)
Feed on gumweed (Grindelia squarrosa) & Dieteria canescens (both Asteraceae). Sexual forms recorded.
Atarsos grindeliae apterae are medium sized, coloured shining pale yellow to pale green with pale to dusky appendages. Aphids in all stages completely lack tarsi, with only a small pulvillus-like pad on the distal end of each tibia. Antennae 6-segmented, shorter than the body, with numerous secondary rhinaria on segments III-V; terminal process a little longer than the base segment VI. Dorsum & appendages moderately hairy, all capitate. Siphunculi short, tapering, without flange. Gillette (1911)
Aulacophoroides4 spp. Taiwan, China, Hong Kong, Korea
Feed on Fabaceae, including bush clover (Lespedeza), Wisteriopsis, and Wisteria.
Rather large aphids, coloured dark red, black or shining green. Antennal tubercles developed and rough, median frontal tubercle little-developed. Head & antennal tubercles spinulose ventrally. Apterae have few secondary rhinaria on antennal segment III, alatae somewhat more. Abdomen of apterae with pronounced marginal sclerites, often also dorsal segmental brown bars. Siphunculi dark pigmented, usually about 2-3 x cauda, with both pre- and post-siphuncular sclerites. Resemble Megourella, but antennal tubercles in Megourella almost completely devoid of spinules. Qiao et al (2006)
Feed on great variety of hosts. Most species host specific, but some highly polyphagous and important crop pests. Monoecious holocyclic, but pest species may be anholocyclic. Do not host alternate and not ant attended.
Medium sized aphids, with pear-shaped bodies. May be yellowish, green, reddish or brown; often have dark green or brownish patch at base of each siphunculus. Antennal tubercles well developed, spiculose, & with near parallel inner sides. Antennae usually longer than body; apterae with 1-3 rhinaria on segment III. Siphunculi quite long, cylindrical or slightly swollen, usually without subapical reticulation. Cauda usually tongue-shaped. Blackman (2010)
Two species feed on honeysuckle (Lonicera, Caprifoliaceae) (primary host ?), and one on Heracleum, Apiaceae) (secondary host ?). Avicennina are mainly found in mountainous areas.
Apterae are rather large, green with or without darker markings. Antennal tubercles high, diverging; frons has a wide groove & barely noticeable median tubercle. Antennae shorter than body; segment III without secondary rhinaria in aptera. Hairs on body, legs & antennae long & capitate. Marginal tubercles absent. Siphunculi long, asymmetrically swollen in middle, with convex opercula. Cauda short, rounded-triangular, shorter in length than width at base, with long hairs. Narzulikov (1957)
Berberidaphis1 sp. mountainous Tajikistan, E Kazakhstan, N Pakistan
Berberidaphis lydiae feeds on undersides of leaves of various different Berberis spp. (Berberidaceae) growing in mountainous areas in Central Asia.
Apterae medium sized, & shiny pale yellow. Antennal tubercles of medium height, slightly diverging; median frontal tubercle very small. Antennae 6-segmented, shorter than body; secondary rhinaria present on segment III in aptera. Body hairs blunt or slightly capitate. Siphunculi sharply swollen in distal half. Cauda rounded conical, length shorter than width at base. Resembles Liosomaphis, but Berberidaphis have better developed antennal tubercles, longer antennae and a short rounded cauda. Narzikulov & Umarov (1969)
Both species, Bipersona ochrocentri & Bipersona torticauda, feed on thistle (Cirsium, Asteraceae) and probably other related genera.
Rather large aphids, normally dark red to brownish grey, with immatures pink, orange or red. Antennae shorter than body, with both apterae & alatae having numerous secondary rhinaria on antennal segment III, and variable numbers on segment IV; alatae have a few on segment V. Siphunculi dark brown to black with fine polygonal reticulation on the apical portion. Cauda elongate, tapering with 4-8 hairs and 3 constrictions making it appear convoluted. Anal plate has a distinctive conical posteriorly directed projection. Thought to be related to Artemisaphis and Obtusicauda.Hottes (1926)
Blackmania eastopi feeds on horsetail knotweed (Polygonum equisetiforme, Polygonaceae).
Apterae medium sized, red-brown in life. Body oval, frons flat without antennal tubercles. Antennae 5-segmented, without secondary rhinaria in apterous viviparae. Terminal process at least 3 x as long as base in aptera (5 x in alate). Body strongly sclerotized. Marginal tubercles absent. Siphunculi straight & flask-shaped. Cauda absent. Genus similar to Acaudella with respect to lack of cauda, but distinguished by strongly sclerotized body, straight siphunculi, & much longer terminal process. Kanturski & Wieczorek (2015)
Some species host alternate, with plum (Prunus, Rosaceae) as primary host; secondary hosts include Asteraceae, Boraginaceae, & Caryophyllaceae. Other species monoecious on variety of plant genera such as aconite (Aconitum, Ranunculaceae) and plantain (Plantago, Plantaginaceae). May be attended by ants. Some important crop or fruit tree pests.
Apterae rather small to medium-sized, green, brown or black aphids. Antennal & median tubercles weakly developed. Antennae shorter than body; apterae lack secondary rhinaria. First tarsal segments have 3,3,3 or 4,4,4 hairs. Spiracular apertures rounded. Abdominal dorsum in apterae often extensively sclerotized, never mealy or waxy. Siphunculi rather short, smooth surfaced, with subapical incision below flange. Cauda very short, often semicircular. Blackman (2010)
Brachycolus mostly feed on pinks (Caryophyllaceae), galling the leaves; possible Chinese species feeds on a Bupleurum (Apiaceae). Monoecious holocyclic. Not attended by ants.
Narrowly oval, green aphids, powdered with wax. Frontal tubercles absent. Antennae 6-segmented, much shorter than body, with terminal process much longer than base segment VI. Antennal segment III of aptera has only short hairs, and no secondary rhinaria. Apical rostral segment shorter than second hind tarsal segment. First tarsal segments have 3,3,2 hairs. Abdominal dorsum of aptera membranous. Unpaired supracaudal process occasionally present on tergite VIII. Siphunculi very short, asymmetrical with small aperture, no flange, and sited on posterior part of tergite V. Cauda triangular or tongue-shaped, much longer than siphunculi. Blackman (2010)
Feed on Asparagus spp. (Asparagaceae) causing severe stunting and 'rosetting' of leaves. Monoecious holocyclic.
Rather small wax-coated aphids, similar in appearance and characteristics to Brachycolus. However, both antennae and terminal process are shorter. Head lacks antennal or median tubercles. Antennae of apterae lack secondary rhinaria. Hairs on dorsal body & appendages very short. Siphunculi extremely short, sited behind the border between abdominal segments V & VI, as in Diuraphis.. Cauda long & finger-like. Blackman (2010)
Primary host probably Neillia (Rosaceae) as oviparae found on it; secondary host is yellow jasmine (Jasminum humile, Oleaceae) where it feeds on leaves and young shoots.
Single species in genus, Brachymyzus jasmini, is medium sized, with head, thorax and antennae blackish brown, abdomen greenish. Antennal tubercles low but distinct, scabrous & Myzus-like. Tergum in aptera pale and membranous. Siphunculi thick and truncate, Brachycaudus-like, with poorly developed flange & without preapical circumcision. Cauda short, with basal half expanded, more or less globular, distally narrow and bluntly conical. Basu (1964)
Brachysiphoniella montana mainly anholocyclic on grasses (Poaceae), especially aquatic species. In Korea evidence of host alternation to pear (Pyrus, Rosaceae). Brachysiphoniella apiaca feeds on wild celery (Apium graveolens in Apiaceae).
Rather small aphids with oval, not elongate body, brownish green, densely covered in mealy wax. Antennal tubercles absent in aptera. Antennae much shorter than body, and 6-segmented;terminal process longer than base of antennal segment VI. No prominent hairs on body. Wings of alate have media vein twice forked, hind-wings have 2 obliques. Siphunculi very small, as long as or a little longer than wide, broadest at the base, and without constriction. Cauda large and very long, with a constriction about middle. Brachysiphoniella genus is closely related to Brachycolus, but distinguished by the structure of the siphunculi, and the larger cauda. Takahashi (1921)
Most feed on Brassicaceae, but some on other plants e.g. Chenopodium (Amaranthaceae). Monoecious holocyclic. Not attended by ants. One species is important pest of cabbage (Brassica) crops.
Medium-sized aphids, grey or green with dark head. Body covered with greyish-white mealy wax. Antennal & median tubercles very low, smoothly rounded. Antennae 6-segmented, usually about half as long as body, with unusually long segment III, Antennae of apterae lack secondary rhinaria; alatae have numerous rhinaria on segment III. Dorsal body hairs pointed, moderately long. First tarsal segments have 3,3,2 or 3,3,3 hairs. Siphunculi are dusky or dark, barrel shaped with a small flange & usually somewhat shorter than cauda. Cauda short, broad and triangular. Blackman (2010)
Feed on Tamarix spp. (Tamaricaceae). Aphids are attended by ants.
Rather small aphids, brown or green, with blackish-brown dorsal spots; covered with wax secretion. Body broadly oval, with weak marginal tubercles only on prothorax. Eyes lack
ocular tubercles. Antennae 6-segmented, with terminal process not longer than base of segment; sometimes rhinaria on segment III of aptera. Siphunculi swollen, shorter than cauda. Cauda broadly conical. Genus resembles Brachyunguis but eyes lack ocular tubercles. Blackman notes that spiracles on abdominal segments 1 and 2 widely spaced; indicates genus perhaps in Aphidini. Nevsky (1929)
Feeds on Chinese mugwort (Artemisia argyi, Asteraceae).
Brevisiphonaphis hirsutissima is medium sized. Colour in life unrecorded. Antennal & medial tubercles undeveloped. Antennae 6-segmented. Long fine hairs on body and appendages. Dorsum not sclerotized, apart from very light brown band on tergite VIII and peritremes (= plates surrounding spiracles). Siphunculi extremely short, slightly conical, without flanges, no trace of polygonal reticulation. Stekolshchikov & Qiao (2008)
Feeds on the fern Davallia chaerophylloides (Davalliaceae) which is epiphytic on oil-palms.
Only species Burundiaphis autriquei rather large, shining greenish black. Head without spiculation. Antennae longer than body; antennal segment I very long, III shorter than IV & V. Apical rostral segment with broad and obtuse apex, & numerous short stiff hairs. Dorsal cuticle membranous. Siphunculi very long, without subapical reticulation. Superficially resembles Paczoskia in general form, but differs in all other characters. Often occurs in mixed colonies with Micromyzella, but that has different apical rostral segment, & dorsal cuticle is often sclerotized. Remaudiere (1985).
Feed on goldenrod (Solidago, Asteraceae). Monoecious holocyclic.
Apterae rather small, with body green or yellow; with or without black dorsal shield. Apical rostral segment rather long and slender, without needle-like tip, with 3 pairs of hairs near apex. Abdominal dorsum in apterae strongly sclerotic. Marginal tubercles absent. Siphunculi have double swelling, first in middle and second as apical knob, with definite constriction separating the two. Cauda is conical. Apically knobbed siphunculi resemble those of Epameibaphis aphids, but Cachryphora lack the stiletto-shaped apical rostral segment of anthemid-feeding aphids. Shape of siphunculi rules out Rhopalosiphum.Oestlund (1887),Oestlund (1923)[1922]
Only species, Campanulaphis radicivora, lives and feeds on roots of bellflowers (Campanula, Campanulaceae). Colonies usually ant-attended.
Apterae with rather large, egg-shaped, dark brown to blackish body. Antennal tubercles low & divergent. Antennal terminal process more than 5 x base segment VI. Secondary rhinaria in aptera on segments III & IV. Rostrum very long, reaches behind of hind coxae. Dorsal hairs pointed. Siphunculi subcylindrical with distinct flanges, with reticulated zone. Cauda cone-shaped with pointed apex. Single distinct process on anal plate. Similar to Uroleucon but differs by presence of secondary rhinaria in apterous females on antennal segments III-IV, & presence of process on anal plate. Kadyrbekov (2016)
Some species host alternate from oleaster (Elaeagnaceae) to daisies (Asteraceae) or knotweeds (Polygonaceae); others live year round on primary or secondary host. Holocyclic. Not usually ant attended.
Apterae small to medium-sized; pale greenish, yellowish, or almost translucent, slender, with elongate legs and antennae. Head has well developed antennal tubercles. Antennae usually 6-segmented, with very long terminal process. Apical rostral segment with pointed apex, and only 2 shortish accessory hairs on basal part. Dorsal abdomen membranous. Dorsal hairs conspicuously capitate, arising from tuberculate bases. Siphunculi long and slender, cylindrical or slightly swollen on distal part. Cauda tongue shaped or triangular, much shorter than siphunculi. Winged viviparae have short hairs & dark dorsal abdominal patch. Blackman (2010)
Only species, Capraphis blackmani, feeds on leaves of the umbellifer Mulinum spinosum (Apiaceae). Monoecious holocyclic.
Apterae are medium sized, coloured yellow or pale green. They have long, curved, rather rigid antennae, described as 'resembling the horns of a goat'. Secondary rhinaria present only on antennal segment III in both apterae and alatae. Without ocular tubercles (triommatidia). Spiracles on abdominal segment II very close together. Dorsum pale in both apterae and alatae. Hairs mainly short. Siphunculi lacking apical reticulation, slightly and asymmetrically swollen, lacking subapical incision, with thick flange. Mier Durante & Nieto Nafria (2009)
Most species host alternate between sumac (Rhus) or poison ivy (Toxicodendron) (both in Anacardiaceae) and sedges (Cyperaceae). Some anholocyclic on Rhus, others in warmer climates persist parthenogenetically on Cyperaceae.
Apterae green, black, red or yellow; those species on Toxicodendron diversilobum aposematically coloured. Antennal tubercles weakly developed. Apterae generally have five antennal segments, alatae have six. Terminal process elongate. Apical rostral segment approximately cylindrical, less than twice as long as basal width. Hind wings one oblique vein (subgenus Carolinaia) or two (subgenera Glabromyzus & Juncomyzus). Siphunculi either swollen in the middle (Carolinaia and Glabromyzus) or more or less cylindrical (Juncomyzus). Cauda is 0.25 x siphunculi and tapering. Wilson (1911)
Only two species in genus: Catamergus fulvae which feeds on impatiens (Impatiens, Balsaminaceae) and Catamergus kickapoo which feeds on Solomon's seal (Polygonatum, Polygonaceae).
Pear-shaped medium-sized aphids. Antennal tubercles well-developed, and front of head convex. Apical rostral segment slender and conical. Marginal tubercles are present on prothorax and usually abdominal segments II-VII. Siphunculi slender, cylindrical, equal to or slightly longer than cauda, without hairs, with imbrications, and with 1 or 2 subapical rows of reticulations, and a very narrow flange. The cauda is elongate, broadly rounded apically, and the anal plate is entire. Catamergus aphids are similar to Macrosiphum, but distinguished by shorter, nearly flangeless siphunculi, and few reticulations on siphunculi. Oestlund (1923)[1922]
Host alternate from various willow (Salix, Salicaceae) species as primary host to various umbellifers (Apiaceae) as secondary host. Most species retain sexual stage in the life cycle. Not attended by ants.
Small to medium-sized green, straw-coloured or ochreous-reddish aphids. Body rather elongate and a little flattened. Antennal tubercles low. Antennae short in apterae, longer in alatae. Cuticle in apterae strongly sclerotic, but not pigmented. Winged forms have trapezoidal black patch on dorsum in front of siphunculi. Supracaudal process on precaudal tergite, usually diagnostic for the genus. Siphunculi cylindrical or clavate with small rim at apex, very distinctly longer than cauda, which is rather blunt. Blackman (2010)
Two species in genus living on hosts in different families: Cedoaphis incognita on snowberry (Symphoricarpos, Caprifoliaceae) and Cedoaphis maxsoni on buckwheat (Eriogonum, Polygonaceae) & daisies (Asteraceae). Monoecious holocyclic
Frontal tubercles weakly to moderately developed. Secondary rhinaria numerous on antennal segments III-V. Terminal process is greater than 4 x base of antennal segment VI. Hind tibia has pseudosensoria basally. Abdominal tergites I-VII have large shallow or flat round marginal tubercles. Siphunculi cylindrical, and imbricated. Cauda relatively short, and helmet-shaped. Validity of genus questionable, but still accepted. Oestlund (1923)[1922]
Host alternate between Viburnum (Adoxaceae) as primary host, and sedges (Cyperaceae) as secondary host. Holocyclic. Not attended by ants.
Small to medium-sized, shiny black, oval aphids. Antennal tubercles undeveloped or very weakly developed, not projecting beyond convex middle part of front of head in dorsal view. Antennae about 0.5 x body, but with long terminal process. Antennae of apterae have few secondary rhinaria on segment III (alatae numerous rhinaria on III-V). Dorsal abdomen is sclerotic and dark, with reticulate pattern formed by small spinules Siphunculi are entirely dark, very scabrous, often somewhat swollen in middle, with very well developed flange. Cauda tongue shaped to triangular. Blackman (2010)
Two species Chaetomyzus rhododendri & Chaetomyzus rhododendrophila, both feeding on Rhododendron (Ericaceae). Life cycle unknown, but may host alternate to sowthistle (Sonchus, Asteraceae).
Rather small aphids. Head with prominent diverging antennal tubercles with low rounded median frontal tubercle. Pleural & spinal tubercles (also described as scabrous dorsal processes) on abdominal dorsum with acute or acuminate hairs. Spinules in transverse rows in apical portion of tibiae and on tarsi. First tarsal chaetotaxy 3,3,3. Siphunculi swollen on both sides. Few caudal hairs. Perhaps related to Indomasonaphis.Ghosh & Raychaudhuri (1962)
Feed on leaves & young shoots of rose (Rosaceae). Holocyclic. Not attended by ants.
Rather small, spindle-shaped aphids, coloured pale yellow to green. Head has well developed antennal tubercles and fairly large median tubercle. Antennae usually 6-segmented; terminal process usually quite long. Apterae lack secondary rhinaria. Rostrum rather long. First tarsal segments have 5,5,5 hairs. Dorsal hairs of apterae capitate, usually arising from tubercular bases. Dorsal cuticle densely covered with small warts. Siphunculi pale and cylindrical. Cauda elongate triangular, much shorter than siphunculi. Alatae have much shorter non-capitate hairs, large dark dorsal abdominal patch and dark wing veins. Blackman (2010)
Feed on Amaranthaceae including sea-blight (Suaeda), saltwort (Salsola) & Bassia. Monoecious holocyclic. Aphids live in dense colonies on plant stem.
Rather small, with apterae pale green or yellowish green and red eyes; apices of appendages darker. Frons with noticeable rounded median tubercle, but very low antennal tubercles. Antennae 6-segmented, with terminal process 1.45-1.75 x base of segment VI. Secondary rhinaria absent. Rostrum reaches hind coxae, with apical rostral segment elongated, stylet-shaped. Cuticle coarsely reticulated. Transverse rows of thickened hairs with mostly fan-shaped apices on tergites I-V, located on small tubercles. Siphunculi semi cylindrical, compressed before rims. Cauda elongate-conical with pointed apex. Kadyrbekov (2002),Nevsky (1928)
Only species, Chakrabartiaphis hydrangeae, induces reddish tubular marginal leaf pseudogalls galls on upper surfaces of leaves of Hydrangea anomala (Hydrangeaceae).
Apterae rather small. Head with well developed antennal tubercles, but no mid-frontal tubercles. Antennae 6-segmented, shorter than body; secondary rhinaria absent in aptera, on segments III & IV in alatae. Dorsal abdominal hairs numerous in both apterae & alatae, long with flagellated apices. Siphunculi cylindrical. Cauda bulbous medially, abruptly narrowed down to form tube-like structure. Very similar to Eumyzus, but has longer, finely pointed dorsal hairs and cauda similar to that of moss-feeding aphids. Chakrabarti & Bhattacharya (1982)
Feed on stem base and roots of daisies (Saussurea, Carduus, Cirsium, Doellingeria, Aster, Kalimeris, Asteraceae). Ants often build an ants nest around the aphid colony.
Most species medium sized, yellowish-green or whitish-green with dark sclerotised dorsal abdominal patch. Antennal tubercles low and diverging, with granules, small spines & scales; median tubercles little developed. Antennae shorter than or equal to body length, with long terminal process; secondary rhinaria on basal half segment III. Apical rostral segment long and conical. First tarsal segments with 3,3,3 hairs. Dorsum extensively sclerotized. Siphunculi cylindrical with 2-3 rows of reticulation at apex, and distal part heavily imbricated. Cauda short & dark. Somewhat resembles Aulacorthum, but adapted for root feeding & ant attendance. Yuan & Xue (1982),Pashtenko (2000)
Chondrillobium1 sp. S Europe to Russian Volga region & Kazakhstan
Only species, Chondrillobium blattnyi feeds on leaves of Chondrilla juncea (Asteraceae), causing yellowing of leaves. At slightest disturbance aphids drop to the ground. Not visited by ants.
Apterae medium sized, pale green with slightly yellowish head and cauda, and darker appendages. Eyes large & protruding, without triommatidia. Antennal tubercles prominent, medial frontal tubercle undeveloped. Antennae slightly less than, or equal to body length, with long terminal process. Antennal hairs very short; hairs on dorsum even shorter. Rostrum not reaching middle pair of coxae, with apical rostral segment slightly longer than second hind tarsal segment. Without papillae or abdominal tubercles. Cauda with 4-9 long pointed hairs. Bozhko (1961),Nieto Nafria (1974)
Only species, Chusiphuncula sorbarisucta, feeds on false spiraea (Sorbaria sorbifolia, Rosaceae). Life cycle unknown.
Apterae are medium sized and green. Head has well developed, smooth antennal tubercles and median frontal tubercle. Antennae 6-segmented, 1.45 x body, with terminal process about 4.6 x base segment VI. Rostrum reaches middle coxae, with apical rostral segment 1. 6 x basal width of segment. Siphunculi obviously swollen, strongly con0stricted below flange, 0.36 x body, and 3.8 x cauda. Cauda pentagonal. Rhopalosiphoninus is similar, but has rough antennal tubercles, siphunculi are shorter (0.20-0.33 x body), and cauda is triangular. Blackman in AWP commented that probably more closely related to Wahlgreniella.Zhang & Chen (1998)
Clypeoaphis1 sp. Europe, N Africa, Middle East, C Asia, Korea
Only species, Clypeoaphis suaedae, feeds on seablite (Suaeda, Kochia,Salsola, Amaranthaceae). Monoecious holocyclic. Not attended by ants.
Apterae small, coloured pale grey-green, with wax powdering. Antennal tubercles absent. Front of the head convex. Clypeus is dark and bulbous. Antennae usually six-segmented & much shorter than body. Siphunculi are short, with weak flange. Cauda is thumb-shaped, and longer than siphunculi. Blackman (2010)
Only species, Codonopsimyzus sasammi, feeds on undersides of leaves of Codonopsis lanceolata (Campanulaceae).
Apterae medium sized, milky white with black antennal joints and tarsi. Antennal tubercles developed, but no median frontal tubercle. Antennae longer than body, with terminal process about 4-6 x base of segment VI. Antennal segment III has row secondary rhinaria. Apical rostral segment is obtuse, wedge shaped. All dorsal hairs blunt, not capitate, very short. Siphunculi slightly swollen or almost cylindrical, cauda short, round at apex with 9-12 long hairs. Alate is pale yellow with large dark dorsal patch; siphunculi and legs blackish. Latter similar to genus Cryptomyzus, but differs from that genus by very short, non-capitate hairs and absence of median frontal tubercle. Lee (2002)
Coloradoa30 spp. Orig. Europe & Asia, now N America
Monoecious holocyclic on chamomiles (Anthemideae, Asteraceae). Feed mainly at shoot apices, or on edges of leaves.
Small green, brown or reddish, globose aphids. Have very convex frons, with no antennal tubercles. Antennae always shorter than body, and terminal process always longer than base of last antennal segment. Antennae of apterae lack secondary rhinaria. Apical rostral segment acutely pointed with concave sides. First tarsal segments have 3,3,2 hairs. Dorsal body hairs short or very short, expanded at tip. Siphunculi cylindrical or slightly swollen, generally with weak flange. Cauda tongue-shaped or triangular. Blackman (2010)
Only species, Corylobium avellanae, feeds on hazel (Corylus, Betulaceae). Monoecious holocyclic. Not attended by ants.
Apterae rather large spindle-shaped aphids, usually green, sometimes reddish; siphunculi pale with dark apices. Antennae longer than body, with very long terminal process; antennae of apterae have few secondary rhinaria base of segment III. Rostrum rather long; apical rostral segment long and slender. Dorsal cuticle with numerous capitate hairs arising from tubercles; also a dense covering of small warts. Siphunculi long and thin. Cauda very short and triangular. Blackman (2010)
European & American species live concealed on the basal parts of grasses (Poaceae). Five Asian species feed on mints (Lamiaceae) and geraniums (Geraniaceae). Monoecious holocyclic.
Frontal tubercles well developed. Antennae 6-segmented, longer than body. Both apterae & alatae have few secondary rhinaria on antennal segment III. Tergum uniformly sclerotic with long, stiff, slightly capitate hairs, not placed on tubercles; such hairs also present on antennal segment III and femora. Siphunculi cylindrical, not reticulated at apex, with very well developed flange. Similar to Metopolophium, but has well developed median tubercle and capitate hairs. Alatae have disc of abdomen sclerotic, but with visible segmentation; same type of long hairs as apterae. Hille Ris Lambers (1947),Blackman (2010)
Cryptomyzus aphids commonly host alternate from currants (Ribes, Grossulariaceae), where they are a pest, to members of mint family (Lamiaceae). Some species live continuously on one or other.
Apterae are spindle-shaped, pale whitish, straw-coloured or pale green. Antennal tubercles low & divergent. Antennae long, with long terminal process; antennae of apterae usually have secondary rhinaria on segment III. Body has numerous capitate hairs. Dorsal cuticle of apterae is smooth, colourless and membranous. Winged forms have a blackish dorsal patch in front of siphunculi which may be broken up by colourless lines or patches. Siphunculi slender, very slightly widened distally and longer than cauda. Cauda rather blunt. Blackman (2010)
Cryptosiphum live in red pseudogalls on Artemisia (Asteraceae). Monoecious holocyclic. Not visited by ants
Rather small plump oval aphids that live within galls on mugworts (Artemisia, Asteraceae). Both apterae & alatae are covered in wax. Living in galls has resulted in reduction of appendages. Antennae less than half body length, with terminal process shorter than base of last segment; secondary rhinaria are absent on apterae. Dorsal hairs very short. Siphunculi very small raised pores, hardly visible. Cauda broadly rounded. Blackman (2010)
Only species, Cyrtomophorodon cyrtomophitum, feeds on fern Cyrtomium falcatum (Drypoteridaceae).
Apterae medium-sized, yellowish-white in life with dark dorsal markings. Antennae longer than body. Rostrum reaches hind coxae. First tarsal chaetotaxy 2,2,2. Large dark spinopleural dorsal patches from mesonotum to tergite IV forming dorsal patch; further patches & bands on posterior tergites. Siphunculi long barrel-shaped, reticulated near apex, 3 x as long as cauda. Cauda nearly tongue shaped with 5 thick, short hairs. Thought to be related to Nearctaphis and Aulacorthum. Blackman in AWP commented it may belong in Micromyzella.Zhang & Qiao (2000)
Only species, Davatchiaphis persica, feeds on upper sides of leaves of common reed (Phragmites australis var. stenophyllus, Poaceae). Oviparae and apterous males have been found in November.
Apterae medium sized, pale green, matt, elongated, fusiform, 3.0-3.5 x longer than wide. Has digitiform Phorodon-like processes on antennal tubercles. Antennae are 5-segmented, about 0.33 x body length, with terminal process longer than base of segment V; secondary rhinaria absent. Antennal hairs very short, only 0.25 x basal diameter of segment. Rostrum short, reaching middle coxae. Siphunculi reduced to circular pore. Cauda lanceolate in shape, narrowed very near base, broadly rounded at apex, and with many strong lateral hairs. Somewhat resembles Brachycolus, but has processes on antennal tubercles. Remaudiere (1964)
Only species, Decorosiphon corynothrix, feeds on mosses (Polytrichum, Atrichum), especially common haircap moss (Polytrichum commune, Polytrichaceae). Sexual forms unknown, overwinters parthenogenetically. Not attended by ants.
Apterae rather small, shiny olive, brownish yellow or reddish brown. Antennae 6-segmented, somewhat longer than body. Antennal segment I has low conical hair-bearing process on inner side; terminal process is pointed. Long, stiff, erect hairs on body, antennae and legs. First tarsal segments have 3,3,2 hairs. Openings of spiracles kidney-shaped. Marginal tubercles on thorax and abdomen absent. Siphunculi longer than cauda, markedly swollen on distal half, and with large flange. Cauda has basal part broad, and distal part slender (like other moss-feeding aphids). Alatae have large, dark dorsal abdominal patch. Blackman (2010)
Two species feeding on members of the carrot family (Seseli, Peucedanum, Apiaceae). Oviparae & alate males in October.
Apterae medium sized, green, either shining green or mottled green with slight whitish pulverulence.
Body narrow. Forehead broad, without median frontal protuberance. Antennae terminal process about twice as long as base. Siphunculi about as long as cauda, with opening protruding cap-like, as in Aspidaphis and Muscaphis. Similar to Hyadaphis bupleuri but without median frontal tubercle. Borner (1952)
Only species, Delfinoia peruviana, feeds on vine Cayaponia sp. (Cucurbitaceae).
Apterae rather large, thought to be pale green, with dusky/dark siphunculi. Antennal tubercles moderately divergent, median frontal tubercle small. Antennae long, with long terminal process. Primary rhinarium has thick, nonciliated edge; secondary rhinaria absent. Siphunculi long, moderately swollen. Cauda triangular, relatively short. Most similar to Wahlgreniella, but that genus has primary rhinaria with ciliated rim. Nieto Nafria & Mier Durante (2017)
Feed on aconite (Aconitum) and Delphinium (both tribe Delphiniae, Ranunculaceae). Often feed amongst flowers. Monoecious holocyclic.
Apterae large, often with aposematic colouration because they sequester toxins from host plant. Antennae have very long terminal process, & numerous secondary rhinaria in both apterae and alatae. First tarsal segments have 3,3,3 hairs. Thoracic spiracles are much larger than abdominal ones. Dorsal cuticle of aptera membranous; alate has pale marginal and intersegmental sclerites. Siphunculi usually dark at least distally, quite long, often with swollen section at about midlength. Cauda dark. Blackman (2010)
Live without host alternation on grasses (Poaceae), usually rolling or otherwise distorting and/or discolouring leaves. Diuraphis noxia is very damaging to wheat and barley, infested leaves rolled into tubes and desiccated, infested ears become bent.
Rather small, narrowly oval aphids, usually yellowish or greenish. Frontal tubercles very low or absent. Antennae 5- or 6-segmented, much shorter than body, with rather short terminal process. Secondary rhinaria absent in apterae; few on antennal segment III/IV in alatae. First tarsal segments have 3,3,2 hairs. Dorsum of aptera membranous. Siphunculi very short, or just as raised pores.
Blackman (2010)
Durocapillata utahensis feeds on rabbitbrush (Chrysothamnus viscidiflorus, Asteraceae). Feeding curls leaves and distorts young growth. Sexuales present in late September-October.
Apterae medium sized, shining yellow-green with black tips to antennae, legs and siphunculi. Antennal tubercles moderately prominent. Rather few secondary rhinaria present on antennal segment III in both apterae and alatae. Rostrum reaches beyond second pair coxae. Body and appendages armed with prominent bristly hairs, most of them noticeably enlarged at tip. Siphunculi large, cylindrical with pronounced constriction before prominent flange. Cauda conical with one or two globate sensilla in addition to long, tapering ones. Knowlton (1927)
Dysaphis105 spp. Mainly Europe to E Asia. Some are cosmopolitan
Host alternate between Amygdaloideae (Rosaceae) and umbellifers (Apiaceae) and other families. Spring colonies distort and discolour leaves. Colonies attended by ants. Several species are important pests of fruit trees.
Medium-sized, plump-bodied, greenish, bluish or pinkish grey in colour and covered in wax meal. Median and antennal tubercles only weakly developed. Antennae 5- or 6-segmented, with quite long terminal process. Secondary rhinaria absent in apterae; numerous in alatae. Apterae typically have dark transverse bars on posterior abdominal tergites; alatae usually have large dark dorsal patch. Marginal tubercles on prothorax and most abdominal segments; conspicuous paired spinal tubercles on head and VIII. Siphunculi rather short, tapering. Cauda short and usually helmet-shaped. Cauda form and spinal tubercles most reliable distinguishing characteristics. Blackman (2010)
Eichinaphis feed on Amaranthaceae in dry or desert environment. Not attended by ants.
Apterae are rather small, pale greenish brown to dark brown, with pair of dark spots on dorsal abdomen. Antennal tubercles poorly developed, median tubercle higher than antennal tubercles. Antennae 6-segmented, shorter than body, without secondary rhinaria in aptera. Rostrum elongate, sharp wedge-shaped. Number of hairs on first tarsal segments 2,2,2. Body dorsum completely sclerotized. Dorsal body hairs long stiff, thick and capitate with tubercle at base. Siphunculi short barrel-shaped, swollen medially, with developed flange. Cauda tongue-shaped. Related to Chaitaphis.Zhang et al. (2016)
Elatobium10 spp. Mainly Europe to E Asia, one is cosmopolitan
Live on spruce (Picea) and fir (Abies) (both Pinaceae). Cryptic when feeding. Do not host alternate. Some species have retained sexual stage, others have lost it. Not attended by ants. One species is important pest of spruce.
Small elongate-oval usually green aphids with rather short appendages. Frontal tubercles little developed. Antennae 6-segmented, shorter than body, and without secondary rhinaria in aptera. Dorsal body hairs short, blunt or rod-shaped. First tarsal segments have 3,3,3 hairs. Dorsal cuticle rather rugose. Dorsum without dark markings in either apterae and alatae. Siphunculi cylindrical, long, thin and pale, with well developed apical flange. Cauda finger-shaped with slight constriction. Blackman (2010)
Feed on wild rose (Rosa, Rosaceae). Previously assumed to be monoecious, but may host alternate with mountain tobacco (Arnica, Asteraceae).
Only species, Eomacrosiphon nigromaculosum, is medium sized, bright red with black patches. Antennal tubercles of aptera are very distinct. Antennal segment III is constricted at base to just over half its diameter slightly nearer apex. First tarsal segments have 5 hairs. Conspicuous marginal tubercles present on pronotum, and most of abdominal segments I to VII. Siphunculi unusually thick, cylindrical or slightly tapering, very densely and heavily imbricated. Forewing of alate has apical pigmented spot. Hille Ris Lambers (1958)
Epameibaphis aphids feed on Artemisia and Seriphidium (Anthemidae, Asteraceae). Most likely all monoecious holocyclic.
Rather small brown or greenish aphids, with frosted appearance due to pale dorsal hairs. Vertex nearly flat. Few, or no, secondary rhinaria on apterae. Have typical stiletto-shaped apical rostral segment of aphids feeding on Anthemideae. Hairs on body are long, many of them blunt, enlarged, or flattened at tip. Siphunculi cylindrical with conspicuous knob-shaped apex. Related to Pseudoepameibaphis,Flabellomicrosiphum and Coloradoa.Oestlund (1923)[1922],Knowlton & Smith (1936)
Most species feeding on heaths (Ericaceae), some on plants in Rosaceae and Liliaceae. Some American species introduced to Europe. Not attended by ants.
Rather small pale green or brown, often shiny aphids. Antennae 6-segmented, shorter than body. Apterae have no secondary rhinaria; alatae have few on segment III only. First tarsal segments have 3,3,3 or 5,5,5 hairs. Dorsal body hairs are short and blunt. Dorsal cuticle of apterae wrinkled or corrugated. Apterae lack dark dorsal markings; alatae have dark dorsal abdominal patch. Siphunculi cylindrical or tapering, often slightly curved outwards at end. Cauda finger or tongue-shaped. Blackman (2010)
Ericolophium13 spp. E Asia, India to Taiwan, one now in Europe
Mainly feed on Rhododendron (Ericaceae), one Indian species lives on willow (Salix, Salicaceae). Host alternation suspected, but no secondary hosts yet identified.
Elongate oval aphids, most species green or greenish brown, often with black dorsal markings. Antennal tubercles and median frontal tubercles well developed. Apterae without secondary rhinaria. Apical rostral segment a little longer than second hind tarsal segment. Siphunculi cylindrical with large flange. Cauda elongate. Chaetomyzus and Indiaphis closely related. Tao (1963)
Eucarazzia2 spp. Mediterranean & Asia, now cosmopolitan aside from Australasia
Only species, Eucarazzia elegans, feeds on mints (Mentha) and other Lamiaceae. Anholocyclic in warm humid climates, but holocyclic where hot summer and cold winter.
Rather small oval green aphids, with distinctive large swollen siphunculi. Antennal tubercles well developed, not converging, and quite smooth like head. In alate, veins of wings all have dark spot where reach margin of wing, but veins not bordered with brown or black. In aptera abdominal tergum membranous; in alatae there is central sclerite. Siphunculi very strongly swollen, with few rows of hexagonal reticulation at the apex. Cauda minute, very short and rather acute. Blackman (2010)
Only species, Eumaerosiphum viciae, feeds on Vicia faba (Fabaceae). There being no known specimens this should be treated as nomen nudum (Aoki, pers. comm.). It may have been a misidentification of Megoura crassicauda / japonica (shown here).
Eumaerosiphum aphids have a green body and a cauda of normal type. Head with well-developed antennal tubercles. Siphunculi are black, which distinguishes them from Macrosiphum euphorbiae.Shinji (1932)
Eumyzus12 spp. Pakistan, India, E Siberia to Japan
Three species on woody Rosaceae in spring in India migrate to unknown secondary hosts. Three species on Impatiens (Balsaminaceae) and two on Hydrangea (Hydrangeaceae) gall their hosts.
Eumyzus are small to medium sized aphids. Head in apterae strongly spinulose. Antennal tubercles divergent. Antennae shorter than body. Dorsal hairs rather long and stiff, usually with tuberculate bases. Abdomen membranous, sometimes with warty corrugations. Siphunculi short, mostly densely imbricated, with or without a flange and never bearing any reticulation. Cauda conical, elongate usually with apical constriction. Diversity within genus rather high, may need revision. Chakrabarti & Bhattacharya (1985)
Only species, Ferusaphis xanthinae feeds on young shoots and undersides of leaves of Manch rose (Rosa xanthina, Rosaceae).
Apterae medium sized, coloured leaf green. Antennal tubercles with finger-shaped processes, inner edges almost parallel, with 4 hairs. Antennae about 0.67 x body length, with terminal process about 2.9 x base antennal segment VI. Tergum strongly wrinkled. Siphunculi swollen, about 0.25 x body length and 3.80 x cauda. Cauda tapered, with constriction in middle and 6 hairs. Zhang et al. (1999)
Rather small aphids with frosted appearance. Antennal tubercles only slightly developed. Rostrum with typical stiletto-shaped apical rostral segment of aphids feeding on Anthemideae. Hairs on body & appendages broadly fan-shaped (= flabellate), giving frosted appearance. Marginal tubercles not evident. Related to Epameibaphis,Pseudoepameibaphis and Coloradoa. Should perhaps be considered as Pleotrichophorus with very short siphunculi. Gillette & Palmer (1932)
Fullawaya species are monoecious on willow (Salicaceae), living on roots.
Apterae rather large, covered with short fine hair. Frontal tubercles very indistinct. Antennae less than half as long as body. Rostrum reaching nearly to tip of abdomen. Marginal tubercles on prothorax & abdominal tergites. Siphunculi much reduced or absent. Genus very similar to Plocamaphis, but characterised by lack of siphunculi, & numerous dorsal abdominal hairs. Essig (1912)
Gibbomyzus pteridophytorum species feeds on ferns (Blechnum,Pteridium, Polypodiopsida). Gibbomyzus polita feeds on Jungia polita (Asteraceae). In both cases host list likely to be incomplete.
Apterae medium sized, pale green or brownish green with pale brown appendages. Antennal tubercles with inner faces divergent, median frontal tubercle shorter. Ventral margin of antennal socket carries protuberance. Hairs on dorsum and (most) appendages short and blunt. Extensive black dorsal abdominal sclerite on raised part of dorsum. Siphunculi swollen, with no apical reticulation. Cauda lanceolate. Nieto Nafria (2013)
Glendenningia1 sp. W USA, British Columbia, Canada
Only species, Glendenningia philadelphi feeds on Philadelphus lewisii (Hydrangeaceae). Only alatae present when species first found and described. Suggests that migration was occurring to an unknown secondary host.
Alatae have head without prominent antennal tubercles. Antennae 6-segmented, with circular rimmed secondary rhinaria in alate. Wing venation normal, with media twice branched. Siphunculi enlarged basally, swollen in apical half, and constricted before flange; longer than cauda. Cauda unusual - it is breast-shaped with a drawn out conical tip. Footit & Richards (1993)
Only species, Gredinia pilosotuba feeds on saw-wort (Saussurea pulchella, Asteraceae).
Apterae rather large, & shining black. Head with diverging antennal tubercles. Antennae slightly longer than body, with secondary rhinaria on segment III. Head & thorax sclerotized, with large thoracic spiracles. Possibly related to Delphiniobium, but has 5 hairs on first tarsal segments, and tapering siphunculi bearing hair. Blackman notes genus is described from only 2 specimens and may be Macrosiphoniella lazoica (found on same host). Pashtshenko (2000)
Only species, Gypsoaphis oestlundi, feeds on honeysuckle (Lonicera, Caprifoliaceae)
Apterae medium sized, pale green wax-covered aphids. Antennal tubercles weakly developed. Antennal terminal process is elongate. Secondary rhinaria circular, in apterae sometimes present on antennal segment III, in alatae on III and IV. Large marginal tubercles on prothorax & abdominal segments II-VI. Siphunculi reduced to pores. Cauda semicircular to tongue-shaped. Related to Palaearctic genera Hyadaphis and Semiaphis, but differs in having poriform siphunculi, rounded cauda & many marginal tubercles. Oestlund (1923)[1922]
Hayhurstia1 sp. Europe, Asia, N&C Africa, N&C America
Only species, Hayhurstia atriplicis, lives in rolled leaf pseudogalls on orache (Atriplex) & goosefoot (Chenopodium) (both Amaranthaceae). Monoecious holocyclic. Thought to be an important vector of plant viruses.
Apterae medium sized, blue-green & heavily wax-powdered. Antennal tubercles undeveloped. Antennae shorter than body, with terminal process more than twice base segment VI; apterae without secondary rhinaria, alatae with rhinaria on III & IV. First tarsal segments have 3,3,3, hairs. Siphunculi very small, shorter than cauda & slightly swollen. Cauda finger-shaped. Blackman (2010)
Only species, Helosiphon eryngii, lives on eryngo (Eryngium campestre, Apiaceae), at bases of petioles and at stem bases, attended by ants.
Apterae medium sized, yellow to grey-green orange with dark appendages, sometimes with reddish area anterior to siphunculi. No distinct antennal tubercles. Antennae with secondary rhinaria on antennal segment III, sometimes on IV. Very large flattened marginal tubercles on pronotum, and segments I-IV & VII. Siphunculi have apices narrowed, surmounted by hemispherical cap, in centre of which opens atrophied pore. Anal plate trapezoidal in shape, widening at posterior edge. May be related to Anuraphis.Leclant (1969)
Only species, Hillerislambersia darjeelingi, first reported on honeysuckle (Lonicera, Caprifoliaceae), but later from Stauntonia (= Holboellia) latifolia (Lardizabalaceae) and Rhododendron (Ericaceae). Life cycle unknown.
Apterae rather large, pale green, with longitudinal dark green stripe on each side of thorax and anterior abdomen. Head with low diverging antennal tubercles. Antennal segment III with few rhinaria. Tergum pale membranous; clothed with very long hairs with finely drawn out apices. Siphunculi quite long & stout, widest at base, narrowest before flange, slightly expanded again on distal half, with preapical part reticulated. Cauda tongue-shaped, usually shorter than basal width. Characterised by long body hairs, stout siphunculi and short cauda. Basu (1968)[1967]
Only species, Himalayaphis anemones, reported to feed on Anemone (Ranunculaceae). Life cycle unknown.
Adult apterae very large and greenish. Head with distinct frontal tubercles. Antennae long and slender, without secondary rhinaria in aptera. Abdominal dorsum papillated. Dorsal hairs long with knobbed apices and tuberculate bases. Siphunculi distinctly swollen without reticulations. Cauda elongate with many fine hairs. Papillate body, long antennae, and capitate hairs suggest relationship with Chaetosiphon, and tuberculate bases to hairs is similar to Ericolophium (=Neoacyrthosiphon). Ghosh & Verma (1973)
Only species, Holmania chaetosiphon, feeds on cinquefoil (Potentilla, Rosaceae). Life cycle unknown.
Apterae medium sized, pale, with dark joints to antennal segments, and dark antennal terminal process, femoral and tibial apices, and tarsi. Dorsum has long thick capitate hairs. First tarsal segments have 5 hairs. Apical rostral segment relatively long & hairy. Siphunculi with hairs and polygonal reticulation. Blackman & Eastop (1982-)
Hyadaphis19 spp. Mostly Europe, Asia, a few cosmopolitan
Some species host alternate between honeysuckle (Caprifoliaceae) and various umbellifers (Apiaceae). Others complete their entire life cycle on honeysuckle. Several species are pests, such as Hyadaphis coriandri on coriander.
Medium sized elongate-oval pale aphids, usually dusted with wax. Antennal tubercles undeveloped. Antennae shorter than body, often with very narrow terminal process; apterae without secondary rhinaria. Siphunculi quite long, but similar in length to the unusually long cauda, usually slightly swollen in middle or distal part, with an apical flange. Cauda dark or pale, tongue- or finger-shaped, at least 1.4x its basal width in dorsal view. Blackman (2010)
Three American species thought to host-alternate between woody Rosaceae (usually Crataegus) and secondary host plants (e.g. Lamiaceae, Onagraceae) (none verified by host transfer tests). Other species known only from herbaceous plants.
Most species have prominent antennal tubercles that may or may not be convergent, and always lack any long finger-like projections. Most species of Hyalomyzus have strongly spinulose heads. Alatae of all Hyalomyzus (except H. monardae) have many secondary rhinaria on antennal segments III- V. Abdominal dorsum of alatae without any pigmented sclerites. Abdominal dorsum of apterae with irregular polygonal inscriptions. All first tarsal segments in adults with 3 hairs. Hyalomyzus apterae have moderately long, swollen siphunculi. Stoetzel et al. (1999)
Only species, Hyalopteroides humilis, lives in colonies along midline on uppersides of leaves of cocksfoot grass (Dactylis glomerata, Poaceae). Monoecious holocyclic, anholocyclic in some countries. Not attended by ants.
Medium sized elongate-oval green aphids. Antennal tubercles well developed, but rather low. Antennae shorter than body, apterae have 1-7 secondary rhinaria, alatae have 11-20, in each case on segment III. Dorsal cuticle membranous. Siphunculi very short and cylindrical, with barely visible apical flange. Cauda long, tongue-shaped and blunt. Possibly related to Metopolophium.Blackman (2010)
All species monoecious on bedstraws (Galium spp.), living on stems or subterranean parts. Attended by ants.
Pale greenish or yellowish aphids with short, mainly dark appendages. Antennal tubercles undeveloped. Antennae much shorter than body. Apterae with 2-9 secondary rhinaria on antennal segment III, alatae with rhinaria on III & IV. Dorsal body hairs short and blunt. First tarsal segments have 2 hairs. Dorsum membranous, wrinkled, sometimes with dark transverse sclerites on segments VII & VIII. Marginal tubercles often present on prothorax & segments I-IV, never on VII. Siphunculi tapered or slightly expanded distally, often curved inwards, flangeless at apex with small aperture. Cauda finger or tongue-shaped. Blackman (2010)
One species, Hydronaphis impatiens, known to host alternate between witch hazel (Corylopsis, Hamamelidaceae) and roots of Impatiens (Balsaminaceae); other species only recorded from roots of (presumed) secondary hosts.
Head spinulose. Antennae about as long as body, with hairs on segment III about as long as or longer than segment width. Long dorsal hairs on abdomen. Hairs of body and antennae not spatulate at tip. Siphunculi slightly swollen apically. Cauda short, conical or tongue-shaped. Alate viviparous female has large central sclerite on abdomen. Resembles Cryptaphis, but hairs not apically expanded, & siphunculi are clavate. Miyazaki (1971)
Hyperomyzus21 spp. mainly Nearctic, some orig. Palearctic
Some species host alternate between currants (Ribes spp.) and daisies (Asteraceae) or Scrophulariaceae; others monoecious on one or other. All species holocyclic. Not attended by ants.
Medium to rather large spindle-shaped aphids, greenish, yellowish, whitish or black in colour. Antennal tubercles low, divergent, & rounded. Antennae with long terminal process; apterae & alatae with many small secondary rhinaria on antennal segment III. Dorsal hairs usually short, with blunt or slightly expanded apices. Abdominal dorsum membranous, or sclerotic and pigmented. Alatae have black dorsal abdominal markings. Siphunculi rather long, markedly swollen over distal two thirds of length. Blackman (2010)
Idiopterus1 sp. almost cosmopolitan in warmer regions + caves, glasshouses
Only species, Idiopterus nephrelepidis, feeds on numerous fern spp. (Polypodiopsida). Reproduction apparently entirely parthenogenetic, no sexual morphs found.
Rather small aphids Head rough with spicules. Antennal tubercles well developed. Antennae longer than body, mainly white except segment apices, with secondary rhinaria in both apterae and alatae. Antennal hairs very short, dorsal body hairs long & pale with tubercular bases. Dorsal abdominal cuticle with reticulation formed by rows of small spicules. Siphunculi have basal part black, distal part black. Wings have pattern of dark pigmentation and unusual venation. Blackman (2010)
Illinoia41 spp. N America + several spp. now in Europe & Asia
Many species associated with heath and rhododendron family (Ericaceae), others feed on taxonomically diverse plants. Monoecious holocyclic. Not attended by ants. Some species important pests of ericaceous plants.
Medium-sized spindle-shaped aphids, mostly green or yellow, but several with different colour forms. Antennal tubercles are well developed with inner faces divergent; median tubercle may also be developed. Antennae longer than body, with rhinaria on segment III in both apterae & alatae. Dorsal abdomen membranous. Siphunculi swollen on distal part, narrowing to polygonal reticulated subapical part. Cauda shorter than siphunculi, slender and finger shaped. Blackman (2010)
Palaearctic species thought to host alternate between Smilax (Smilaceae) and Impatiens (Balsaminaceae); two invasive species live year round in Europe where produce sexuales on secondary host. American spp. are monoecious holocyclic on Cuphea (Lythraceae).
Medium sized pear-shaped aphids. Most species have shiny black dorsal shield over green body. Head smooth and dark, with well developed antennal tubercles. Both apterae & alatae have secondary rhinaria on antennal segment III or III-V. First tarsal segments have 3,3,3, hairs. Dorsal cuticle strongly sclerotized. Siphunculi black & tapering, cauda pale & tongue-shaped. Blackman (2010)
Live on undersides of leaves of Rhododendron and Agapetes (Ericaceae). Holocyclic with alate males. Not attended by ants.
Apterae medium sized, whitish, yellow or green. Head lacks both antennal & median frontal tubercles. Antennae 6-segmented, with no secondary rhinaria in apterae. Tergum is pale & membranous, bearing rather thin long hairs with finely drawn out apices. Alatae have solid pigmented area from tergites II-V, & transverse bands on tergites I & VI-VIII. Second tarsal segments with spinular imbrication. Siphunculi very thick without flange. Cauda pale and more or less tongue-shaped. Genus closely related to Ericolophium.Basu (1969),Ghosh (1991)
Only species, Indoidiopterus geranii, feeds on Geranium spp (Geraniaceae).
Apterae medium sized. Dorsum of head spinulose. Antennal tubercles with almost parallel margins. Apterae without secondary rhinaria. Hairs on frons, flagellum and body with lanceolate to capitate apices. Hairs on abdominal dorsum on low tubercles. Number of hairs on first tarsal segment 3,3,2. Fore wings of alate with media forked once, radial sector fused in middle with outer branch of media; wing veins bordered brown. Siphunculi slightly clavate on distal half, cauda elongate. Chakrabarti et al. (1972)
Two species host alternating between Rhododendron and Asteraceae.
Apterae rather large to very large, elongate oval, green, yellow or brown in colour; alatae have dark dorsal markings. Antennal tubercles developed and diverging, with median tubercle slightly developed. Antennae of apterae without secondary rhinaria, alatae with numerous secondary rhinaria. Dorsal abdominal hairs, at least spinally, placed on tubercles. Hind tarsi spinulose. Siphunculi cylindrical for basal part, then swollen in middle, before narrowing again to apex. Cauda elongate, tongue shaped with many hairs. Spinulose hind tarsi & numerous secondary rhinaria similar to other Rhododendron feeders Chaetomyzus,Ericolophium & Indiaphis.Verma (1971)
Primary host of 2 species is bladdernut (Staphylea, Staphyleaceae). Populations of one species occur in summer on daylily (Hemerocallis).
Apterae of Indomegoura indica rather large, orange yellow, covered in white wax. Spiracular sclerites of thorax not strongly produced, with openings of normal size. First tarsal segments each have 3 hairs. Siphunculi wholly black, very thick only about 5 x as long as their smallest width on basal half, slightly swollen with maximum swelling near middle of their length, and reticulated at apices. Genus Delphiniobium is somewhat similar to Indomegoura, but has spiracular sclerites of thorax strongly produced, with opening very large and round, and siphunculi slender, paler than cauda basally. Zhang & Qiao (1998)
Only species recognised is Indomyzus sensoriatus. Host plant unidentified. Another species of genus (Indomyzus glaricae Sathe & Jadhav) was recorded as feeding on Gliricidia maculata (Fabaceae), but name and description of aphid were invalid as no type specimens were designated.
Apterae blackish brown. Head spinulose, with low diverging antennal tubercles. Antennal segment III & sometimes IV have secondary rhinaria. Apical rostral segment longer than second hind tarsal segment. Tergum dark sclerotic, with dorsal hairs conspicuous, longer than basal diameter of antennal segment III (similar to Micromyzodium). Siphunculi dark, more or less cylindrical, imbricated, 1.67-2.0 x cauda. Cauda dark, subpentagonal, with 4 hairs. Ghosh et al. (1971)
Ipuka3 spp. Africa, Sri Lanka, China SE Asia, Australia
Feed on various Asteraceae, including tasselflower (Emilia) & squarestem (Melanthera). Apparently anholocyclic.
Apterae brownish grey or greenish yellow to yellowish orange, with dark siphunculi. Head spinulose with slightly diverging antennal tubercles. Antennae longer than body, with abundant secondary rhinaria on both apterae and alatae on segments III & IV(V). Dorsal and antennal hairs short, not capitate. Alatae have forewings with veins dark, and cubital veins slightly clouded. Siphunculi long, almost cylindrical, with indistinct polygonal reticulation. Cauda longer than wide at base. Immatures have spinulose hind tibiae. May be most closely related to Aulacorthum.van Harten & Ilharco (1976)[1975]
Only species, Iranaphias dehbani, feeds on bedstraws (Galium, Rubiaceae). Life cycle is unknown, but probably monoecious, holocyclic.
Apterae rather small, oval, dark-coloured with slight pruinosity. Slightly convex forehead without trace of frontal tubercles. Antennae 5-6 segmented, slightly more than half body length. Secondary rhinaria normally absent. Dorsum has numerous, long pointed hairs, not swollen at apex. Number of hairs on first tarsal segment 3,3,3. Siphunculi extremely short, shorter than diameter, with no flange; operculum reduced to atrophied pore. Cauda rounded, very short, only about half as long as basal width. Shape of siphunculi is Hydaphias-like, but chaetotaxy, length of siphunculi and cauda, and dorsal hairs all differ. Remaudiere & Davatchi (1959)
Jacksonia4 spp. India, China, & temperate oceanic regions
Two species feed on grasses (Poaceae), one on bellflowers (Campanulaceae). Live on concealed basal parts of plants. Oviparae not known, but males described. Not attended by ants.
Apterae rather small to medium sized, brownish, greenish or yellowish. Antennal tubercles well developed, rough and broad, median frontal tubercle not developed. Apterae without secondary rhinaria; alatae have large protuberant rhinaria on antennal segments III-V. No marginal tubercles present. Siphunculi are slender, thinnest in middle, without flange.
Hosts are various grasses (Arthraxon, Digitaria, Microstegium, Poaceae) and bamboo (Phyllostachys). Life cycle unknown.
Kaochiaoja arthraxonis apterae are shining dark brown (or salmon pink to reddish brown) with yellowish brown head; Kaochiaoja sikkimensis are shining black with yellowish brown head. Antennal tubercles well developed, inner sides parallel or slightly diverging. Apterae without secondary rhinaria; alatae with them on III & IV. Dorsum usually with black mark over thorax and most of abdominal segments to form black quadrate patch; alatae have black patch on segments IV-VI. Siphunculi cylindrical, about 1.5 x cauda, with few reticulations at apex, & large flange. Cauda elongate, a little constricted at middle, with hairs on each side below constriction. Similar to Neomyzus, but no secondary rhinaria at base of segment III. Tao (1963)
Only species is Karamicrosiphum humuliosum. Host is Japanese hop (Humulus scandens, Cannabaceae). Life cycle unknown.
Apterae are rather large, with an elongate elliptical body. Antennal tubercles developed, with inner sides diverging. Antennae 0.83 x body, bearing 15 capitate hairs on segment III, as well as 11-12 secondary rhinaria. Rostrum reaches mid-coxae, with apical rostral segment 0.93 x second hind tarsal segment. Dorsal hairs of body capitate at apex. Number of hairs on first tarsal segments 4,4,4. Siphunculi long, about two x cauda, barrel shaped, basal part pale. Cauda long, tongue shaped with 7-8 capitate hairs. Related to Microsiphum, but that genus has dorsal hairs pointed at apex, siphunculi shorter than cauda, & cauda short triangular. Zhang (1998)
Feed on stems, flowers and/or leaves of various mints (Dracocephalum, Lophanthus, Nepeta, Salvia, Lamiaceae).
Apterae are medium sized, pale green or whitish yellow. Head smooth with diverging antennal tubercles and well developed median one. Antennae long with secondary rhinaria on segment III only in both apterae & alate. Apical rostral segment very hairy. Body leather-like with smooth dorsum. Body hairs numerous, stout, slightly capitate, and not placed on tubercles. First tarsal segments with 5,5,5 hairs. Well developed spinal tubercles on vertex and some of posterior abdominal segments; marginal tubercles on prothorax and segments II-V. Siphunculi more or less cylindrical, with distinct flange. Forewings of alatae with brown-bordered veins. Close to Cryptomyzus, but that has long capitate hairs on tubercles, chaetotaxy of 3,3,3 or 3,3,2 hairs, and often slightly swollen siphunculi. Szelegiewicz (1979)
Only species, Kugegania ageni, feeds on etiolated parts of various grasses (Digitaria abyssinica, Leersia hexandra, Pennisetum clandestinum, Poaceae).
Apterae are rather small aphids. Antennal tubercles well developed, inner sides parallel. Pair of spinal tubercles present on head. Antennae 6-segmented, without secondary rhinaria in apterae, with 1-4 rhinaria on segment III in alatae. First tarsal segments have 3,3,2, hairs. Dorsum pale, weakly reticulated. Siphunculi dusky, very slightly swollen, with distinct imbrication and flange; they are about 2.25-2.75 x cauda, which bears 5 hairs. Alate has reduced wing venation with radius usually absent, once branched media, and no oblique veins on hindwings. Alate has no dorsal abdominal pigmentation, except for narrow band on tergite VIII. Eastop 1955
Only species, Landisaphis davisi has goosefoot (Chenopodium, Amaranthaceae) as its natural host, but also found on various members of cabbage family (Brassicaceae), including peppergrass (Lepidium), tansymustard (Descurainia) & shepherd's purse (Capsella).
Body broadly oval to pear -shaped. Vertex convex, antennal tubercles only slightly developed. Antennae 5 or 6 segmented, about 0.5 x body length. Abdominal dorsum reticulate. Bears at least 5 pairs of prominent marginal tubercles. On tergites VI-VIII there are rugose conical spinal tubercles (less developed in alatae), on which mostly spatulate hairs are borne. Siphunculi clavate. Similar to Hyalopterus, but antennal tubercles little developed. Knowlton & Shihchun Ma (1949)
Only species, Lehrius papillicaudus, feeds on Vietnamese balm Elsholtzia pseudocristata (Lamiaceae). Life cycle unknown.
Apterae have well-developed antennal tubercles. Siphunculi without flange. Cauda has basal part broad, and distal part slender. Apparently close to Jacksonia. Blackman in Aphids on Worlds Plants comments it could be Myzus isodonis.Blackman & Eastop (1982-)
Lepidaphis2 spp. Uzbekistan, Turkmenistan, S Kazakhstan, Xinjiang-Uygur region, W China
Only two species in genus, Lepidaphis deformans and Lepidaphis terricola, both feeding on peppergrass (Lepidium, Brassicaceae), former in leaf galls, latter on roots.
Apterae are medium sized, spindle shaped aphids, greenish with light wax coating. Antennae & median tubercles are hardly visible, with 12-16 hairs on front of head. Antennae are short, 0.25-0.38 x body length, with terminal process short; without secondary rhinaria in aptera, only on segment III in alate. First segment of tarsi has 3,3,2 hairs. Dorsal cuticle reticulated, dorsal hairs thickened. Marginal tubercles absent. Tergite VIII has 12-20 hairs. Siphunculi short, only 0.55-0.75 x cauda, conical or keg-shaped with small but distinct flange. Cauda is triangular and bears 6-10 long hairs. Related to Brevicoryne and Brachycolus.Kadyrbekov & Shao (2002)
Only species, Linaphis lini, feeds on common flax (Linum usitatissimum, Linaceae). Can cause serious damage to flax crop.
Apterae are medium sized, grass-green. Median frontal tubercle no higher than antennal tubercles, with 2 short conical tubercles on ventral side of head. Antennae 0.33 x body length, with terminal process about 1.3 x base segment VI. Rostrum only reaches base of midcoxae. Body hairs short, thick and capitate. No marginal tubercles. Siphunculi cylindrical, slightly swollen at distal end. Cauda conical with 4 hairs. Alate vivipara has no secondary rhinaria on antennal segment IV. Resembles Spatulophorus and Micraphis.Zhang (1981)
Monoecious holocyclic on bedstraws (Galium, Rubiaceae). Not attended by ants.
Apterae shiny green spindle-shaped aphids, with rather long appendages. Immatures waxy. Head smooth with well developed, diverging antennal tubercles. Antennae 6-segmented, longer than body, without secondary rhinaria in aptera, only few on segment III in alate. First tarsal segments have 3,3,3 hairs (fore-mid-hind). Dorsal cuticle of aptera smooth and slightly sclerotic; alatae have only dark marginal sclerites & small intersegmental sclerites. Siphunculi pale or dusky, becoming darker towards apex; tapering or cylindrical, often slightly swollen proximal to subapical, reticulated zone. Cauda pale & finger-shaped. Blackman (2010)
Monoecious holocyclic on barberry (Berberis, Mahonia, Berberidaceae). Not attended by ants. One species is pest of ornamental barberry bushes.
Medium-sized aphids, generally reddish, yellowish or greenish. Head smooth, with antennal tubercles weakly developed. Antennae much shorter than body; secondary rhinaria only on alate on segments III-V. Dorsum unpigmented in apterae, some pigmentation in winged forms. Siphunculi markedly clavate and swollen, with maximum width of swollen part broader than base. Cauda tongue-shaped, longer than basal width, with 5-6 hairs. Blackman (2010)
Lipamyzodes1 sp. Britain, Lebanon, Washington, USA
Only species, Lipamyzodes matthiolae, recorded feeding on diverse plant genera, mainly in Brassicaceae - (Arabis, Cardaria, Lepidium, Matthiola), but also bedstraw (Galium, Rubiaceae), horned poppy (Glaucium, Papaveraceae) and yarrow (Achillea, Asteraceae). Life cycle unknown.
Apterae medium-sized, green or blue-green, lightly dusted with wax. Head spinulose, with well developed frontal tubercles. Antennae shorter than body, without secondary rhinaria in apterae, in alatae on segments III (and sometimes IV). First tarsal segments have 3,3,2 hairs. Antennal & body hairs short with expanded apices. Dorsum of aptera somewhat sclerotic but unpigmented; alate has dark central dorsal patch on tergites III-VI. Siphunculi cylindrical, but often with slightly swollen distal part (as in Lipaphis); more distinctly swollen in alate. Cauda broad-based, bluntly triangular, bearing 5 hairs. Genus thought to be most closely related to Myzus.Blackman (2010)
Lipaphis aphids feed without host alternation on members of cabbage family (Brassicaceae).
Small to medium-sized greyish or brownish green aphids, sometimes wax powdered. Head spinulose with variably developed frontal tubercles. Antennae shorter than body, without secondary rhinaria in aptera; alate has rhinaria on segments III-IV or III-V. Dorsal body hairs very short. Dorsum of aptera sclerotic with varying degrees of pigmentation and sclerotization. Alatae may have a complete series of abdominal cross bands or may have such bands only on posterior tergites. Siphunculi are cylindrical or slightly swollen on distal part. Cauda broad-based, tongue shaped or elongate triangular with 4-6 hairs. Blackman (2010)
Only species, Longicaudinus corydalisicola, feeds on various Corydalis spp (Papaveraceae). Life cycle unknown. Native to Japan & Taiwan, but recently recorded as invasive in Europe (Spain, Britain).
Apterae are medium sized, spindle-shaped, green. lightly covered with wax powder. Antennal tubercles low. Antennae about 0.7 x body length, with terminal process 2.0-2.6 x as long as basal part of segment VI. Apterae without rhinaria; alatae with 6-9 on segment III. Rostrum reaches middle coxae. First tarsal segments have 3,3,3 hairs. Apterae have abdomen sclerotized and pigmented pleurally, without marginal tubercles; alatae have large rectangular sclerite extending on tergites III-VI. Siphunculi tapering, 0.67-0.75 x cauda, with distinct flange. Cauda elongate conical, round at apex, with 6 hairs. Immatures pale greenish yellow. Longicaudus similar, but differences in antennal morphology and first tarsal chaetotaxy. Miyazaki (1971)
Copyright Juan Ramon Vazquez Mora, all rights reserved.
Most species host alternate between rose (Rosa, Rosaceae) and members of buttercup family (Ranunculaceae).
Apterae generally small to medium sized, pale coloured and lightly wax-dusted. Antennal & median frontal tubercles absent. Antennae shorter than body, with unusually long segment III and short terminal process. Apterae lack secondary rhinaria, alatae have very many on III, but none on IV or V. First tarsal segments have 6,6,6 hairs. Dorsum of apterae pale membranous, alatae with broad transverse sclerites on III-VI. Siphunculi cone-shaped or cylindrical, usually very short (may be absent in fundatrices) with small flange. Cauda long and finger-shaped, with many hairs. Blackman (2010)
Only species, Loniceraphis paradoxa, feeds in spring on primary host - honeysuckle (Lonicera, Caprifoliaceae), attended by ants. Secondary host not known. Holocyclic with sexuales in early October.
Only species, Loniceraphis paradoxa, has rather large lightly waxed, whitish green fundatrices. Antennal tubercles very low, with diverging inner edges; no median frontal tubercle. Antennae 6-segmented, shorter than body; segment III shorter than segments IV & V combined, & terminal process about 3 x base of segment VI. Rostrum very short, not reaching mesocoxae. No marginal tubercles. Siphunculi thin, cylindrical, slightly widened at base. Cauda short, broadly triangular, with 6 hairs. Emigrant alatae have green abdomen, with large black spot on dorsum on tergites II-V. Secondary rhinaria on segments III & IV. Narzikulov & Umarov (1969)
Both species of Macchiatiella associated with buckthorn (Rhamnus, Rhamnaceae) and knotweed (Polygonum, Polygonaceae). Host alternation probable between these two plant genera.
Medium sized aphids, apterae are yellow-brown or yellow-green with black markings. Antennae longer than body, with very long terminal process. Apterae have secondary rhinaria on antennal segment III, and alatae on III-IV (-V). Abdomen may or may not have a complete sclerotic patch joined to marginal sclerites. Spiracles of abdominal segments I and II are well separated. Siphunculi tapering, & rather short for Macrosiphini. Cauda is arc-shaped or rounded, very short. Blackman & Eastop (1982-)
Macromyzella celticola, feeds on hackberry (Celtis, Cannabaceae); Macromyzella polypodicola, feeds on ferns (e.g. Asplenium, Cheilanthes, Christella). Life cycle uncertain.
Apterae of Macromyzella polypodicola are yellow, orange or cream-coloured, with black siphunculi and cauda. Head slightly convex at middle of front, antennal tubercles developed, but median tubercle low. Antennae are without secondary rhinaria on segment III; terminal process about 6 x base of segment. Apical rostral segment about 6 x second hind tarsal segment. Abdominal dorsum is unsclerotized apart from large brown postsiphuncular sclerites on tergite VI. Dorsal hairs on anterior segments short, about 0.5 x middle diameter of antennal segment III, and without scleroites at bases. Resembles Macromyzus, but Macromyzella has shorter hairs and unsclerotized dorsum. Takahashi (1963) (as Macromyzus polypodicola).
Copyright Takuro Tsukiji, Mushinavi all rights reserved.
Macromyzus aphids feed on various genera of ferns (Polypodiopsida). Anholocyclic on ferns in most places, but in Japan though to be partially heteroecious as alate spring migrants have been described from Hydrangea.
Medium to large Asian fern-feeding species. Apterae yellowish or brownish. Head has dorsum and venter spinulose. Antennal tubercles developed, with inner margins diverging. Antennal segment III in apterae with or without secondary rhinaria; segments III & IV in alatae have round protruberant secondary rhinaria. Number of hairs on first tarsal segment 4,4,4 or 4,4,3. Dorsal cuticle rugged with raise dark scleroites. Siphunculi cylindrical with spinulose imbrications and 6-10 rows of reticulation at apex. Cauda in aptera coniform, in alate more elongated, with 4-6 hairs. Su & Qiao (2010)
Macrosiphoniella162 spp. N Hemisphere, a few becoming cosmopolitan
Live on Anthemideae (Asteraceae), especially Artemisia, Achillea etc. Monoecious holocyclic. Not attended by ants. Can be important pests of herbs and chrysanthemum.
Medium to rather large aphids, oval to spindle-shaped, coloured green to brown, frequently bearing conspicuous wax pattern. Usually with well developed, divergent antennal tubercles. Antennae longer than body, with long terminal process; secondary rhinaria on segment III in apterae, III-IV in alatae. Apical rostral segment often stiletto shaped. First tarsal segments have 3,3,3 hairs. Dorsum not sclerotic, if pigmented then only on small scleroites. Siphunculi long, flangeless and more or less cylindrical. Reticulate zone covers about one quarter length of siphunculi. Blackman (2010)
Macrosiphum152 spp. Most in N America / Europe, others Asian + poss. S America
On rose (Rosa, Rosaceae) & many other hosts including teasels (Dipsacaceae), umbellifers (Apiaceae), valerians (Valerianaceae) and buttercups (Ranunculaceae). Few species (e.g. M. rosae, M. pallidum) host alternate from Rosa to other hosts, but most monoecious holocyclic. Not attended by ants.
Medium to large spindle-shaped green and/or pink aphids, with long legs and antennae. Antennal tubercles rather high, smooth, and divergent, median tubercle undeveloped. Antennae long with terminal process more than 3 x base of segment VI; secondary rhinaria on segment III in both apterae & alatae. First tarsal segments have 3,3,3 hairs. Siphunculi long, not swollen, with flange, & with zone of regular polygonal reticulations covering 0.10-0.17 near end of siphunculus. Cauda always pale and very elongate. Immatures thinly waxed. Blackman (2010)
Only two species in genus: M. yatsugatakensis maybe feeding on mugwort (Artemisia),
M. rarissima on apical leaves of saw-wort (Saussurea) (both Asteraceae). Biology unknown.
Apterae medium sized, dark brown. Antennal tubercles low, strongly diverging at inner sides. Antennae are long; apterae have secondary rhinaria on segment III. Number of hairs on first tarsal segments 5,5,5. Body densely hairy, the hairs being very long and flagellate. Abdomen membranous, with ante- and postsiphuncular sclerites well developed, without scleroites on anterior segments. Siphunculi elongate, cylindrical, reticulated at apex, with many hairs. Related to Macrosiphoniella, but they have 3,3,3 hairs on first tarsal segments. Also related to Uroleucon, but neither body nor siphunculi in that genus are very hairy. Miyazaki (1971)
Only species, Mastopoda pteridis, is holocyclic, (possibly) host alternating between leaf petioles of Viburnum and ferns, especially bracken Pteridium aquilinum (Dennstaedtiaceae)
Apterae are medium sized, yellowish white with dark pleural markings; light orange shading at base of siphunculi & dusky orange siphunculi. Antennae are 5-segmented, about same length as body, with terminal process about 6.5 x base segment VI. Antennal segment III without secondary rhinaria. Legs unusual, with tarsi very reduced. Siphunculi are cylindrical, about 0.27 x body length. Oestlund (1887)
Copyright David Enrique, no rights reserved
Matsumuraja15 spp. E Asia + 1 in Queensland, Australia
All but one species feed on berries (Rubus, Rosaceae), one reported from fig (Ficus rubis, Moraceae) (may not be true host). Life cycle only known for 1 species which host alternates between Clethra (Clethraceae) and Rubus.
Apterae on the secondary host are brown, orange, pale yellow-green or white. Antennae variable in length, sometimes much longer than half the body length. Usually have tubercle on antennal segment I which is about 0.6 x as long as that segment. Apical rostral segment longer than second hind tarsal segment. Long capitate hairs arise from tubercles, which are often extended into fingerlike processes. Siphunculi sclerotized, and sometimes slightly swollen on distal part. Cauda distinctly longer than wide. Takahashi (1931)
Feed on members of bean family (Fabaceae). Holocyclic, with no host alternation. Not attended by ants. One species is important vector of bean viruses resulting in considerable yield loss.
Medium to large aphids. Head with well-developed antennal tubercles, with inner faces divergent. Antennae about as long as body, bearing secondary rhinaria on segment III in apterae, III-IV in alatae. Antennal and dorsal hairs fairly long. First tarsal segments have 3,3,3 hairs. Dorsum of apterae mainly unmarked. Alatae have large marginal and siphuncular sclerites and cross bands on VII & VIII. Siphunculi usually black & somewhat swollen in middle, cauda long, finger-shaped & hairy. Blackman (2010)
Two species in genus, (Megourella purpurea and Megourella tribulis) which live on stems of vetchlings (Lathyrus) and vetches (Vicia) (Fabaceae). Sexual morphs develop in autumn.
Rather large, oval, swollen aphids. Large, diverging antennal tubercles, no median frontal tubercle. Antennae about as long as body with secondary rhinaria on segment III in all morphs. First tarsal segments have 3,3,3 hairs. Abdominal tergum in both apterae and alatae membranous, with longitudinal rows of spinal, marginal and pleural sclerites bearing hairs with slightly expanded apices. Also siphuncular sclerites and cross bands on posterior tergites. Siphunculi sclerotic black, slightly swollen, attenuated towards apex. Cauda elongate, shorter than siphunculi and much paler. Blackman (2010)
Only species, Megourina lagacei, feeds on columbine (Aquilegia formosa, Ranunculaceae); biology unknown.
Differs from Megourella by having median frontal tubercle distinct, and 4-5 hairs on first tarsal segments. Also has long, somewhat capitate hairs, with marginal ones placed on domed sclerites, and yellow instead of black tibiae. Alatae have 47-55 secondary rhinaria on antennal segment III, and dark, not bordered wing veins. Perhaps most closely related to nearctic Nasonovia (Kakimia).Hille Ris Lambers (1974)
Only fully accepted species in genus is Meguroleucon codonopsicola which feeds on Codonopsis (Campanulaceae). Life cycle unknown. Meguroleucon longqishanense seems questionable (see Blackman in AWP).
Apterae medium sized, yellowish green with milky tint, brown head, black siphunculi, very large black postsiphuncular sclerites, & pale cauda. Antennal tubercles high, diverging at inner sides; median tubercle not developed. Antenna black, long, with secondary rhinaria only on segment III in both apterae & alatae. First segment of all tarsi with 4 hairs. Abdomen membranous, with marginal and siphuncular sclerites well developed, without scleroites or marginal tubercles. Siphunculi subcylindrical, reticulated at apex, longer than cauda. Miyazaki (1971)
Only species, Metopeuraphis atriplicis, feeds on orache (Atriplex cana, Amaranthaceae). Life cycle unknown.
Apterae green, dusted with greyish wax. Antennal tubercles low & weakly diverging, with no median tubercle. Antennae shorter than body, with terminal process 3 x base of segment VI. Antennal segment III has 1 secondary rhinarium. Rostrum extends beyond base of hind coxae. Dorsal hairs sparse, needle-like with blunt apex. Prothorax and abdominal tergites II-IV usually have well-developed marginal tubercles. Siphunculi cylindrical, with reticulation on apical half, with distinct flange. Cauda short, finger-shaped conical, with weak constriction. Similar to Metopeurum, but that genus is without marginal tubercles. Narzikulov & Smilova (1975)
Most species monoecious holocyclic on daisies (Asteraceae). Have sexual stage in life cycle, overwintering as eggs, but no host alternation. Attended by ants.
Medium-sized to rather large aphids, most species blackish, brown or reddish. Antennal tubercles & median tubercle very weakly developed, Antennae about as long as body, with numerous protruberant secondary rhinaria on segment III or III-IV in apterae, & on III-IV or III-V in alatae. Dorsal body hairs short, not arising from scleroites. Siphunculi thin, dusky or dark over at least half of length, with polygonal reticulation usually extending over more than distal 20%; no distinct flange. Cauda tapering, triangular, rather short and hairy. Anal plate forms conical protrusion below cauda. Blackman (2010)
Metopolophium24 spp. N hemisphere, 1 now in temperate regions worldwide
Some species host alternate between rose (Rosa, Rosaceae) and grasses (Poaceae), overwintering as eggs on rose. Some species anholocyclic on grasses overwintering parthenogenetically.
Medium to rather large aphids, with most species green or yellow green. Apterae have rather low divergent antennal tubercles, & distinct median tubercle. Antennae shorter than or equal to body length. Both apterae & alatae with secondary rhinaria on segment III. First tarsal segments have 3,3,3 or 3,3,2 hairs. Dorsal cuticle sclerotic, pale or smoky. Alatae usually have some dark dorsal markings. Small marginal tubercles often present on tergites II-V. Siphunculi pale, cylindrical, rather expanded at base, not reticulate apically, and with small to moderate apical flange. Cauda elongate, rather blunt. Blackman (2010)
Only species, Micraphis artemisiae feeds on leaves and stems of Artemisia capillaris. Life cycle unknown.
Apterae rather small, yellow or greenish. Frontal tubercles very short. Antenna 0.3-0.4 x body, with terminal process 1.2-2.0 x base of antennal segment VI. Apical rostral segment stout, not stiletto-shaped, same length as second hind tarsal segment, with 2 secondary hairs. First tarsal segments have 3,3,3 or 3,3,2 hairs. Thoracic and abdominal tergites sclerotic, and papillated or corrugated. Dorsal hairs of body minute. Abdominal segment VII roundly produced posteriorly. Possibly related to Coloradoa, but apical rostral segment not stiletto-shaped. Takahashi (1923) as Cerosipha
Microlophium5 spp. Europe to Japan, Burundi, Rwanda, N America, Chile
Monoecious holocyclic on nettles (Urticaceae). Not attended by ants (unlike Aphis urticata which is nearly always ant-attended).
Apterae rather large, pale brownish-green or reddish, spindle-shaped aphids. Antennal tubercles smooth, with inner faces divergent. Antennae much longer than body length, with secondary rhinaria confined to segment III in both apterae and alatae. Antennal & dorsal body hairs mostly rather short & blunt. First tarsal segments have 3,3,3 hairs. Siphunculi long, 2.3-3.1 x the length of the cauda, tapering with a large flange. Cauda tongue-shaped or triangular. Blackman (2010)
Most feed on ferns (Polypodiopsida), two on Asteraceae. Life cycle unknown.
Apterae medium-sized, often pale green, with dusky or dark dorsal sclerotization, & dark siphunculi. Head with or without spiculation. Secondary rhinaria on antennae III variable - absent in apterae in all but 2 species, always more than 4 on III in alatae, as well as more on IV & V. Apical rostral segment with 3-14 secondary hairs. First tarsal segments with 3,3,3 or 3,3,2 or 2,2,2 hairs. Forewings with 3 branches of media, radial sector weakly curved. Dorsal pigmentation usually present on apterae and alatae. Spinal papillae absent. Siphunculi cylindrical, more or less swollen, with a well marked flange. Similar to Kugegania, but that has different venation of forewings and no secondary hairs on apical rostral segment. Remaudiere & Autrique (1985)
Feed on range of host plants including ferns (Polypodiopsida). Life cycles mostly unknown except for Micromyzodium kuwakusae which has sexual stages on Chinese fringe flower (Loropetalum, Hamamelidaceae)
Apterae yellow or black, with head dark sclerotic with warts. Antennal tubercles prominent, inner sides almost parallel. Antennae longer than body, with terminal process 5.5-7.6 x base of antennal segment VI. Secondary rhinaria absent in apterae, present on segment III in alatae. Dorsal integument sclerotic & deeply pigmented in both apterae & alatae. Dorsal hairs of body thick and long. Siphunculi cylindrical, with constriction below apical flange. Cauda acuminate, with 4-7 hairs. Related to Micromyzus & Micromyzella, but those genera do not have long dorsal body hairs. David (1958),Su et al. (2014)
Micromyzus11 spp. Mostly E Asian, 1 Venezuela, 1 Australia
Feed on ferns (Polypodiopsida). Some species may host alternate, but life cycles mostly unknown.
Apterae medium sized, variably coloured green, yellow, orange, black. Antennal tubercles well developed, inner sides about parallel. Antennae usually longer than body, with long terminal process. Secondary rhinaria absent in apterae, usually only on segment III in alatae. First tarsal segments of fore and mid-legs usually with 4 hairs. Wing venation normal except radial sector is very strongly curved. Wing veins with broad black bands; hind wings with 2 oblique veins. Alatae without dark dorsal central abdominal patch. Siphunculi usually clavate, sometimes near cylindrical. Cauda bears 5-6 hairs. Related to Micromyzella, but that genus has usually has fore and mid tarsi with 3 or 2 hairs. Eastop (1958)
Apparently monoecious on members of pea & bean family (Fabaceae). North American populations usually holocyclic, Central & South American populations probably partly anholocyclic.
Medium-sized brightly-coloured aphids. Antennal tubercles distinct. Antennae six-segmented, with secondary rhinaria on antennal segment III. Wing venation of alatae distinctive. On forewing, radial sector short & strongly curved, media vein typically two branched, & cubital veins heavily shadowed. Hind wing minute; has only radius, without oblique veins; costal hooks very near wing tip. Apterae have marginal tubercles on abdominal tergites II-IV. Siphunculi cylindrical in subgenus Microparsus, but clavate in subgenus Picturaphis. Cauda long and tapering, anal plate hemispherical. Close relationship with Macrosiphum, but differentiated by wing characters. Patch (1909)
All species monoecious holocyclic on different species of wormwood (Seriphidium & Artemisia, Asteraceae).
Apterae mostly rather small aphids, coloured green or brown. Antennal terminal process at least 3 x base of antennal segment VI. Both apterae and alatae have secondary rhinaria on antennal segment III. Apical rostral segment conical, with sides concave to stiletto-shaped. Apterae have completely sclerotic, pigmented tergum. Dorsal hairs quite long. Siphunculi small & short, not longer than wide, less than or equal to 0.5 x cauda. Cauda broadly triangular. Distinguishable from closely related European genus Microsiphum by much longer hairs. Smith & Knowlton (1938) (as Microsiphum acophorum).
Monoecious holocyclic mostly on wormwoods (Artemisia) & yarrows (Achillea, Asteraceae). Form ant-attended colonies on stems.
Medium sized, green or reddish aphids with very dark antennae and legs. Frons without distinct tubercles. Antennae as long as body or longer, with secondary rhinaria in apterae and alatae. First tarsal segments with 3,3,3 hairs. Siphunculi very short, not longer than broad at base and truncate or short cylindrical. Hairs rather short, blunt to slightly fan-shaped. Siphunculi very short, frequently with reticulation, and without flange. Cauda broader than long, conical with narrowed tip, with many hairs. In alatae forewings with media twice-forked. Related to Macrosiphoniella, but they have long siphunculi & cauda. Appendages reduced as in other aphids adapted to ant association. Blackman (2010)
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Miyazakia ranunculi is heteroecious holocyclic, host alternating between oriental photinia (Photinia villosa, Rosaceae) (primary host) and mao gen (Ranunculus japonicus, Ranunculaceae).
Apterae medium sized, broadly elliptical, dark reddish brown dorsally, with mainly dark appendages. Antenna 0.5-0.7 x body length; segment III without secondary rhinaria. Body, legs and antennae with long, rigid hairs. Abdomen with tergum uniformly sclerotized, pigmented, smooth, with small marginal tubercles on segments I-V. Siphunculi rather short, gradually tapering or abruptly attenuated on apical half, 2.5-3.5 x as long as wide at base, with 5-8 long rigid hairs & well developed flange. Cauda semi-circular, with 4-6 hairs. Related to Sappaphis, but that does not have strongly sclerotized tergum or rigid hairs. Miyazaki (1971),Stekolshchikov (2014)
Likely that all species host alternate somewhere in their range, but most species only known from primary host hawthorn (Crataegus) & Sorbus, both Rosaceae) or secondary host (mosses, Bryophyta).
Very small, oval, shiny reddish brown or green aphids. Apterae lack antennal tubercles & median frontal tubercle. Antennae short, 5 or 6-segmented, with long pointed terminal process. Secondary rhinaria absent on apterae, present on segments II-V on alatae. Body hairs of adult apterae short & sparse. First tarsal segments have 2 or 3 hairs. Dorsum sclerotic with granulate sculpturing. Siphunculi scabrous, tapering from somewhat swollen base; aperture sometimes subapical, if so tapers to narrow apex. Cauda short with broad base and narrow apex. Blackman (2010)
Feed on knotweed (Polygonum, Polygonaceae). One species feeds on young shoots and under leaves, which are rolled inward.
Apterae rather small to medium-sized, oval in shape, and (in cases known) shiny brownish-black or black in life. Head with rather low but distinct Myzus-like antennal tubercles. Tergum slightly sclerotic and wrinkled. Dossal hairs minute. Stigmal pores of tergites VI & VIII much larger than those on preceding tergites (as in Akkaia). Siphunculi strongly imbricated, gradually tapering, constricted before well developed flange. Cauda elongate heart-shaped to pentagonal. Considered close to Akkaia, but differs in having no frontal processes on antennal tubercles; also cauda not knobbed. Basu (1969)
Myzaphis9 spp. Europe to Asia, 2 near cosmopolitan
Myzaphis aphids feed on rose (Rosa) and cinquefoils (Potentilla), both in Rosaceae. Monoecious holocyclic.
Small spindle-shaped dorso-ventrally flattened green or brown aphids. Head has low antennal tubercles, but strongly projecting median frontal process. Antennae about 0.5 x body length, without secondary rhinaria in apterae, and on III, or III-V in alatae. First tarsal segments all have 5 hairs. Dorsum sclerotic and ornamented with numerous small pits. First tarsal segments are 5-haired. Siphunculi rather long and cylindrical, with distal part often curved outwards & slightly swollen. Cauda is tongue-shaped or triangular. Blackman (2010)
American species thought to host alternate from hawthorn (Crataegus, Rosaceae) to monkeyflower (Mimulus Scrophulariaceae), Veronica (Plantaginaceae) and various moss species (Bryophyta). European & Asian species are monoecious holocyclic or may exist as anholocyclic populations.
Apterae have nodulose head, with well developed, rounded antennal tubercles and median frontal tubercle.
Apterae without secondary rhinaria on antennae; alatae have rhinaria on segments III-V. Number of hairs on first tarsal segments 3,3,2. Abdomen has faint dorsal stripes. Siphunculi subcylindrical, pigmented and usually coarsely imbricated, with length 4.0-6.5 x basal width. Cauda has broad protruding base and shield-shaped medially extended projection. Blackman (2010)
Species in Japan, Myzosiphum ruykyuense feeds on knotweed (Polygonum, Polygonaceae); host of Chinese species unknown. Biology unknown.
Apterae medium-sized; colour of apterae in life unknown. Dorsum of head granulated. Antennal tubercles very developed, protruding forward and almost parallel on inner sides. Antennae 6-segmented, scaly, with terminal process about 4 x base of antennal segment VI. Apterae without secondary rhinaria, alatae with rhinaria on III-V. Antennal and dorsal hairs short & fine. Rostrum stout extending beyond second coxae. Dorsum integument granulated. Number of hairs on first tarsal segments 3,3,3. Siphunculi cylindrical, narrowing towards apex, with 4 rows of reticulations & large flange. Cauda elongate, tongue-like with 3 long hairs on each side. Related to Myzus, but that genus does not have subapical reticulation on siphunculi. Tao (1964)
Only species, Myzotoxoptera wimshurstae, monoecious holocyclic, feeding on stem bases & roots of bittercresses (Cardamine, Brassicaceae) growing in damp areas.
Apterae medium-sized, dark olive green, with blackish strongly spinulose head & dark siphunculi. Antennal tubercles well developed with divergent inner faces, median tubercle undeveloped. Apterae have few secondary rhinaria on antennal segment III, present in alatae on segments III-IV. First tarsal segment have 3,3,3 hairs. Dorsal cuticle has very short sparse hairs & reticulate sculpturing which traps air film when aphid submerged in water. Spiracular apertures covered by opercula. Siphunculi much longer than cauda, cylindrical, with large flange. Cauda short, helmet-shaped with 4 hairs. Blackman (2010)
Myzus69 spp. Worldwide, orig. ? Palaearctic, mostly Asian
In colder climates dioecious holocyclic, alternating between plum species (Prunus, Rosaceae) & great variety of secondary hosts. In warmer climates may reproduce parthenogenetically viviparously throughout the year. Not attended by ants. Three highly polyphagous species are important pests.
Rather small to medium-sized green, yellowish, brownish, or black aphids, sometimes rather flattened. Head with well-developed more or less convergent antennal tubercles. Dorsal cuticle of apterae uniformly sclerotic, from nearly colourless to deep black. Alatae have solid pigmented area on abdominal dorsum, & further segmental bars. Siphunculi rather long, either tapering, cylindrical or clavate, usually distinctly flanged. Cauda acutely triangular. Blackman (2010)
Nasonovia47 spp. Worldwide, but mostly N hemisphere
Host alternate between currants (Grossulariaceae) and various daisies (Asteraceae) especially lettuce (Lactuca), Crepis and Hieracium spp. Not attended by ants. One species is important cosmopolitan pest of lettuce.
Medium-sized green or reddish, rather shiny aphids Distinct but rather low median & antennal tubercles, the latter with divergent inner faces. Antennae usually longer than body with long terminal process; secondary rhinaria on segment III in apterae, and on III-IV or III-V in alatae. Well-marked dorsal sclerotic pattern of pigmented paired intersegmental muscle plates. Alatae often have dark segmental bars connecting the muscle plates on abdominal segments III-V. Siphunculi rather long, cylindrical, with little or no apical reticulation, & with flange. Cauda is elongate, rather blunt finger-shaped and bears 5 or 7 hairs. Blackman (2010)
Nearctaphis14 spp. Most N America, 1 Europe, 1 Worldwide
Most host alternate between apple tribe (Maleae) as primary hosts, and pea family (Fabaceae) or broomrapes (Orobranchaceae) as secondary hosts.
Small to medium sized aphids, mostly coloured dark green, brown or yellow. Antennal tubercles poorly developed. Antennae shorter than the body length; apterae sometimes with secondary rhinaria on antennal segment III; alatae have them on segments II-IV (-V). Dorsum bears long hairs & reticulate pattern of spicules. Apterae often have dark scleroites at the bases of hairs, sometimes fused into larger spots or cross bars. Alatae have dark marginal sclerites and dorsal cross bands, often joined together on tergites IV-VI to form dark patch. Marginal tubercles may be present. Siphunculi short and tapering with close-set rows of small spinules (see also siphunculi in related Anuraphis) and well-developed flange. Cauda short, triangular or helmet-shaped. Blackman (2010)
Only 2 species in genus, Neoamphorophora kalmiae monoecious holocyclic on mountain laurel (Kalmia, Ericaceae) in North America, and Neoamphorophora ledi in Europe & Asia on Rhododendron (Ericaceae).
Medium sized green or brownish apterae, with darker dorsal markings. Antennae shorter than body; apterae without secondary rhinaria, alatae with secondary rhinaria on segments III & IV. Hairs very small & inconspicuous. Rostrum reaches somewhat behind second pair of coxae. Siphunculi of moderate length, rather abruptly swollen, imbricated but not reticulated & with distinct flange, Cauda long and slender, slightly constricted, with 4 hairs. Related to Wahlgreniella but with shorter antennae, shorter terminal process, and apterae have no rhinaria on ANT III. Mason (1924),Heie (1995)
Only two species in genus, feeding on Viburnum (Adoxaceae). May host alternate with sedges (Cyperaceae).
Apterae medium sized, oval-ellipsoid, with pink head, brownish dorsally and pink ventrally on abdomen; antennae dark, siphunculi black. Covered with fine white wax powder. Head with scattered spinules. Antenna nearly half as long as body. Apterae have 0-4 secondary rhinaria on antennal segment III; alatae have rhinaria on segments III-V. Rostrum short, just reaching middle coxa. First tarsal segments all with 4 hairs. Tergum sclerotic, with distinct cell-like reticulation, with abdominal tergites I-VII coalesced. Dorsal hairs numerous, rather large. Flattish marginal tubercles on prothorax and abdominal segments I-V; small spinal tubercles sometimes on VII. Siphunculi covered with rows of minute spinules, tapering, with a distinct wide flange. Cauda dark, rounded, with 10 to 12 long, curved hairs. Genus apparently not accepted as distinct from Ceruraphis by Blackman in Aphids on Worlds Plants. MacGillivray (1960),Stekolshchikov (2022)
Neomariaella1 sp. alpine France, Poland, Slovakia, Turkey, Iran, Kazakhstan, Mongolia
Only species, Neomariaella lambersi, is monoecious holocyclic on young shoots of Myricaria spp. (Tamaricaceae).
Apterae rather small, pale green to yellow, with dark siphunculi & cauda; dusted with grey wax powder. Frons without frontal tubercles. Antennae 5-segmented, about 0.30-0.38 x body, with terminal process 1.13-1.63 x base of segment V. Aptera is without secondary rhinaria; alatae have 9-11 secondary rhinaria on antennal segment III, 2-3 on IV & 1 on V. Antennal hairs short. Rostrum just reaches middle coxae. Dorsal hairs thick and blunt. Tergite VIII and marginal scleroites on tergites V-VII dark sclerotized. Siphunculi truncate with large flange. Cauda short, rounded, about twice as wide as long, with 5-7 hairs. Resembles Protaphis, but lacks marginal tubercles. Possibly related to Brachycolus or Brachycorynella but they do not have short rounded cauda, very short conical siphunculi, or 5-segmented antennae.
Feed on diverse plant genera in several families including Campanulaceae, Hydrangeaceae, Primulaceae, & Orchidaceae. One species, Neomyzus circumflexus, is extremely polyphagous feeding on many different plant species.
Apterae medium-sized, oval, white, green or yellow aphids with distinctive black dorsal markings on apterae. Head strongly spiculose as well as coxae and around siphuncular bases. Antennal tubercles have converging inner sides. Antennae somewhat longer than body, with long terminal process. Aptera has few secondary rhinaria on antennal segment III, alatae on III-IV. Siphunculi rather thick, cylindrical with several rows of flat hexagonal cells below large flange. Immatures have spinulose hind tibiae. Often classed as subgenus of Aulacorthum because of long antennae & siphunculi with large flange. Now considered closer to Myzus because of spiculose head and immatures having spinulose hind tibiae. Blackman (2010)
Two species feed at stem base and roots of willow (Salix), third on poplar (Populus), both in Salicaceae. One species known to be monoecious holocyclic; males only moult once to attain maturity.
Apterae of two species reddish or purplish grey, covered with fine wax powder. Resemble Pterocomma in general appearance and structure with broad body. Head has two dorsal tubercles. Antennae 6-segmented, short with terminal process longer than base of antennal segment VI. Rostrum normal. First tarsal segments have 5,5,5 hairs. Body much less hairy than Pterocomma. Abdomen has two spinal tubercles on each segment. Siphunculi extremely short & atrophied. Cauda rounded & very hairy. Heie (1986)
Neorhopalomyzus2 spp. China, Japan, Korea, E Siberia
Both known species dioecious holocyclic, host alternating between honeysuckle (Lonicera, Caprifoliaceae) and unknown secondary host.
Fundatrices of Neorhopalomyzus lonicericola rather large, dirty yellow, with black-tipped siphunculi. Fundatrices of Neorhopalomyzus lonicerisuctus are dark brown, dusted with white wax powder. Antennal tubercles well developed, moderately projecting inwards. Antennal segment III without secondary rhinaria in apterae, present in alatae. Abdomen of alate with dorsal transverse and siphuncular sclerites. Siphunculi swollen near middle, with some imbrications below flange, much longer than cauda. Cauda tapering, and anal plate broadly rounded. Tao (1963)
Neosappaphis franzi swept in meadow in which sea thrift (Armeria ? maritima, Plumbaginaceae) was dominant. Other known species, Neosappaphis paradoxa, feeds on roots of Sisymbrium polymorphum (Brassicaceae)
Only apterae known. Frons quite straight. Antennae (4)5-segmented, about 0.44-0.50 x body length, bearing secondary rhinaria on antennal segments III & IV; secondary rhinaria present even in immature apterae. Antennal terminal process 2.9-3.3 x base of segment V. Hairs on antennae very short. Granulated integument. Marginal tubercles on abdominal segments I-VII and spinal tubercles irregularly on all segments from vertex to abdominal tergite VIII. Siphunculi quite smooth, without flange and with rounded apex. Near Dysaphis & Anuraphis, but differs in having flangeless siphunculi. These occur in Acaudinum, but that genus has 6-segmented antennae and fewer spinal tubercles. Hille Ris Lambers (1959)
Three species do not host alternate, but spend entire life cycle on onion (Alliaceae), Caryophyllaceae or Violaceae. They have no sexual stage in the life cycle but reproduce all year parthenogenetically. Other three species host alternate from Caprifoliaceae to unknown secondary hosts.
Apterae rather small to medium sized aphids, usually dark reddish brown or blackish brown. Head has pronounced antennal and median frontal tubercles. Eyes large. Antennae in alate female longer than body, with secondary rhinaria on antennal segment III. Wings with the first oblique vein once forked, as in Aphis subgenus Toxoptera; hind wings with normal venation. Wing veins are dark-bordered. Siphunculi fairly long and swollen. Cauda bluntly pointed, shorter than siphunculi. Genus differs from Aphis subgenus Toxoptera in the long antennae and from Rhopalosiphum in anterior wing venation. Theobald (1915),Blackman (2010)
Only species, Nietonafriella euclypteata, feeds on snakeroot (Eupatorium patens, Asteraceae). Colonies live on apices and young stems, with tendency to drop when disturbed. Monoecious holocyclic, with apterous males
Apterae medium-sized, greenish yellow to dark green, sometimes with a darker green, orange or reddish brown band between and around bases of siphunculi. Well developed frontomedial tubercle. Antennae of alatae longer than body, with long terminal process and secondary rhinaria on antennal segment III. Without sclerotization. Hairs generally long and pale, with blunt apex. Number of hairs on first tarsal segments 3,3,3. Clypeus notably enlarged. Long slender siphunculi, pale at least in the basal half, with a reticulated and narrow apical part. Pale and long-triangular cauda. Distinguished from subgenus Lambersius (Uroleucon) by tarsal hairs, from Macrosiphum by caudal shape, and enlarged clypeus. Ortego (1998)
Note: Nietonafriella was synonomized with Uroleucon by Nieto Nafria et al. (2024).
Only species, Nigritergaphis crassisetosa, feeds on Isodon eriocalyx (Lamiaceae).
Apterae medium sized, shining black, with dark siphunculi and a dusky cauda. Median frontal tubercle
poorly developed, antennal tubercles developed. Antennae 5- or 6-segmented, much shorter than body, without secondary rhinaria; alatae have large and round secondary rhinaria on segments III-V. Terminal process about 2-3 x longer than base of the last segment. Apical rostral segment longer than second hind tarsal segment. Number hairs on first tarsal segments 2,2,2. Abdominal dorsum has extensive dark sclerotization. Dorsal body hairs numerous, long, thick, stiff, arising from tuberculate bases. Marginal tubercles absent. Siphunculi short and tapering, slightly swollen towards base, with distinct imbrication and well developed flange. Cauda helmet-shaped, but slightly acute at apex, with 4 hairs. Zhang et al. (2013)
Only species, Nippodysaphis deutziae has Deutzia crenata (Hydrangeaceae) as primary host; secondary host unknown.
Fundatrix without distinct frontal tubercles. Antennae 6-segmented, without secondary rhinaria. No marginal or spinal tubercles. Siphunculi not reticulated, cauda very short. Emigrant alatae with few rhinaria on segment III-IV, first tarsal segments with 4,4,4 hairs, abdomen with Myzus-like dark dorsal abdominal patch Resembles Dysaphis (Pomaphis), but lacks marginal or spinal tubercles, and has first tarsal segments with 4,4,4 hairs. Hille Ris Lambers (1965)
Only species, Nudisiphon folisacculata feeds on Spiraea (Rosaceae), Indigofera (Fabaceae). Cause leaves to fold upwards and parallel to the midrib, forming 'fluffy sac-like pseudogalls'. Holocyclic with alate males.
Apterae medium sized, probably pale, wax covered. They are without antennal and median frontal tubercles. Antennae 6-segmented, shorter than body, with terminal process longer than base of antennal segment VI. Apterae without secondary rhinaria; alatae with numerous secondary rhinaria on antennal segments III-V. Eyes without ocular tubercles. Rostrum reaches beyond mid coxae. Hairs on first tarsal segments 2,2,2. Abdominal tergum membranous. Dorsal abdominal hairs short & pointed. Siphunculi clavate, without flange. Apterae have peculiar cauda with curved, horn-like hairless apex; alatae have elongate triangular cauda with hairy apex. Chakrabarti & Bhattacharya (1982)
Aptera are medium-sized to large, with most species blackish or dark green /brown. Antennal tubercles are moderate sized distinct and divergent. Antennae are 6-segmented, about as long as body. In apterae bear a few secondary rhinaria on antennal segment III; alatae have rhinaria on segments III-V. In alatae forewings have media twice -branched, hind wings have both media and cubitus present. Siphunculi more or less cylindrical. Cauda obtuse, constricted at middle, round at tip - not acuminate as in Macrosiphum and Illinoia. Probably most closely related to Macrosiphoniella.Soliman (1927)
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Only 2 species in genus, Oedisiphum compositarum feeds on cudweeds (Gnaphalium), Oedisiphum soureni feeds on pearly everlasting (Anaphalis) & Gnaphalium, both in Asteraceae.
Apterae are medium-sized, brownish green with dark siphunculi. Most characteristics as in Aphis, but with small marginal tubercles on prothorax, and on abdominal segments IV or V. Usually also 2 small spinal tubercles on segment VIII, rarely also on VII. Apical rostral segment quite long. Siphunculi very short & swollen, about 4 x as long as wide. Cauda broadly plate shaped, somewhat pointed, about as long as wide, and significantly shorter than the siphunculi. Alatae have numerous secondary rhinaria on ANT III-V and an extensive black dorsal abdominal patch. Resemble Brachycaudus but with reniform spiracular apertures, and with long apical rostral segment adapted for feeding on Asteraceae. van der Goot (1917)
Only species, Ossiannilssonia oelandica feeds on northern bedstraw (Galium boreale, Rubiaceae). Monoecious holocyclic with alate males.
Apterae medium-sized, greenish yellow with dusky siphunculi & cauda. Frons almost straight with very low tubercles. Antennae 6-segmented, about 0.5 x body. Secondary rhinaria absent. Rostrum reaches to middle coxae. First tarsal segments have 3,3,3 hairs. Paired spinal tubercles on abdominal tergites III-V and unpaired cauda-like processes on abdominal tergites VI-VIII. The siphunculi are short, strongly curved inwards, and without flanges. Cauda tongue shaped with 6-8 hairs. Heie (1992)
Ovatomyzus have lost sexual stage in life cycle, & are anholocyclic on plants in the mint (Lamiaceae) and borage (Boraginaceae) families. Some species have specialized overwintering morph.
Apterae are small pale aphids with characteristics intermediate between Ovatus and Myzus. Well developed antennal tubercles with slightly diverging inner margins. Antennae are as long as the body or longer with very long terminal process; apterae lack secondary rhinaria, alatae have them on segments III-V. First tarsal segments have 3,3,2 hairs. Siphunculi long, slender, cylindrical or slightly swollen. Cauda tongue shaped, slightly constricted near the base. Blackman (2010)
Ovatus11 spp. Europe to Korea, N Africa, USA glasshouses
Three species host-alternate between hawthorn (Crataegus) or apple (Malus) (both Rosaceae) and mints (Lamiaceae). Other species live all-year-round on former secondary hosts. Not attended by ants. One species is pest of mint.
Small to medium sized greenish aphids. Antennal tubercles well developed & divergent, with additional processes on inner sides of tubercles. Antennae curved and longer than body, with long terminal process; apterae lack secondary rhinaria, alatae have them on segments III-V. First tarsal segments have 3,3,3 or 3,3,2 hairs. Dorsal cuticle rather sclerotic; alatae have dusky or dark marginal sclerites and thin cross bands, but no black central abdominal patch. Siphunculi tapering or cylindrical, never clavate. Cauda short & tongue shaped. Blackman (2010)
Paczoskia9 spp. E Europe, W Asia + 1 unidentified sp. in Ethiopia
Mostly monoecious holocyclic on globe thistles (Echinops, Asteraceae); few on other Asteraceae such as Centaurea and Jurinea.
Rather large aphids, mostly shiny brown. Antennal tubercles are unusually well developed, median frontal tubercle usually absent Antennae 6-segmented, about as long as the body or longer; rather small, protruding secondary rhinaria confined to segment III in alate vivipara. Apical rostral segment very elongated, much longer than second hind tarsal segment, with a large number of short hairs. First tarsal segments have 5 hairs. Tergum membranous with dorsal hairs on scleroites, and with large siphuncular sclerites. Siphunculi have reticulated area wider than part nearer base. Cauda much shorter than siphunculi. Genus related to Macrosiphoniella.Holman (1981),Hille Ris Lambers (1958)
Paducia2 spp. Illinois, New York, Maine, USA, Greenland
Only 2 species in genus, Paducia antennata & Paducia aterrima, both feeding on roots of willow (Salix, Salicaceae).
Apterae medium sized, probably shiny dark brown or black. Antennae four-segmented and much shorter than body. Antennae. legs, and body covered with numerous long hairs. Head very broad and without antennal tubercles. Media of fore wings once-forked, hind wings with both media and cubitus present. Alate vivipara with large well developed marginal tubercles on abdomen. Siphunculi long, greatly swollen, constricted near base and before flange at apex. Cauda elongate, constricted in middle; tip rounded, almost knobbed. Anal plate very broad. (Note: description based on ovipara & alate vivipara). Hottes & Frison (1931)
Only species, Papulaphis sleesmani, feeds on ferns (Adiantum pedatum, Cystopteris bulbifera).
Apterae medium sized, lemon yellow to lemon green. Closely related to Macrosiphum, but with unusual secondary rhinaria. Those on antennal segment III extend over the apical 0.75 of the segment and are located mostly one side. They are small, very tuberculate, and in many cases two or more rhinaria arise from a single base. Apterae have 10-37 rhinaria on segment III, 0-4 on IV; alatae have 35-47 on III, 5-10 on IV. Venation of forewing is also unusual. Radial sector is long, arising well before pointed apex of stigma, & first fork of media nearer base than wing margin. Robinson (1966)
Two species feed on umbellifers (Apiaceae), one on cinquefoils and strawberries (Rosaceae). Monoecious holocyclic on the respective hosts. Not attended by ants.
Rather small pale shiny aphids. Apterae have well developed steep-sided antennal tubercles & long antennae, with long terminal process. Rather large secondary rhinaria present on antennal segment III. Antennal and dorsal body hairs very short. Apical rostral segment much longer than second hind tarsal segment. Siphunculi rather long and straight and slightly swollen with distinct flange. Cauda short and tongue shaped & bears 4-6 hairs. Resembles (but not necessarily closely related to) Myzus.
Only species, Paraphorodon omeishanaensis, feeds on undersides of leaves of bramble (Rubus, Rubaceae)
Apterae rather small, pale green, with dusky antennae. Antennal tubercles have prominent Phorodon-like digitiform process extending forward. Antennae 6-segmented, with terminal process longer than base of antennal segment VI. First antennal segment bears mesial projection. Thoracic & abdominal cuticle densely papillated, & bearing capitate setae. Siphunculi cylindrical, imbricated over whole length, and narrowed backward from mid-point. Anal plate rounded. Alatae undescribed. Tseng & Tao (1938)
Pentalonia4 spp. Worldwide in warm climates & glasshouses
Three species feeding on either banana (Musaceae), ginger (Zingiberaceae) or arums (Araceae). One species holocyclic, two mainly anholocyclic.
Rather small, oval to reddish-brown to blackish aphids. Head spiculose with rather small scabrous antennal tubercles, and no median frontal tubercle. Antennae 6-segmented, about as long as body, with very long terminal process. Apterae have no secondary rhinaria; alatae have few on antennal segments III-V. Antennal hairs short; body hairs short and broadly fan-shaped. First tarsal segments have 3,3,2 hairs. Alatae have distinctive wings, with the forewing veins thickly brown-bordered; radial sector strongly curved, fused with media vein for part of length, forming closed cell. Hind wing reduced, with one oblique vein. Siphunculi rather thick, clavate, black on distal part, and with large flange. Cauda tongue-shaped with 4 hairs. Immatures have spinulose hind tibiae, as in Myzus.Blackman (2010)
Pentamyzus5 spp. 4 in S America, 1 in California, USA
Feed on grasses (Poaceae). One species known to be monoecious holocyclic.
Apterae rather small to medium sized, green, yellow or white. Antennae 5-segmented. Apterae & alatae have secondary rhinaria on antennal segment III. Head Myzus-like, with almost smooth antennal tubercles and a marked median frontal tubercle. First tarsal joints with 3,3,3 hairs. Dorsal & antennal hairs short, not capitate. Apterous viviparae with faintly sclerotic tergum, alatae without a distinct central sclerite on abdominal dorsum. Abdomen in apterae without marginal or spinal tubercles, with the spiracular pores of tergites I and II rather close to each other. Siphunculi clavate, not reticulated at apex. Cauda longer than wide a base. Hind tibiae of larvae not spinulose. Opinions differ on what is most closely related (Carolinaia sstr. or its subgenus Glabromyzus). Hille Ris Lambers (1966)
Phorodon6 spp. Europe, SW Asia, N Africa, N America, New Zealand
Some alternate between blackthorn or plum (Prunaceae) and hops (Cannabaceae). Others feed only on secondary hosts. Not attended by ants. One species, Phorodon humuli, is major pest on hops.
Small to medium-sized aphids, generally green. Cuticle on head spiculose. Characteristic projections on inside of antennal tubercles and on inner side of antenna. Antennae usually 6-segmented, shorter than body, with rather long terminal process. Secondary rhinaria absent in apterae, present in alatae on III-IV(V). Alatae have dark marginal sclerites & dark central dorsal patch. Siphunculi long, tapering, often slightly curved outward distally, and with distinct flange. Cauda short, elongate triangular, with 6-10 hairs. Blackman (2010)
Pleotrichophorus60 spp. Mainly America, plus Europe & Asia, few worldwide
Monoecious holocyclic on Asteraceae, especially in tribe Anthemideae. Not attended by ants.
Medium-sized pale usually green spindle-shaped aphids. Antennal tubercles fairly low, median frontal tubercle moderately developed. Antennae have very long terminal process. Both apterae and alatae have secondary rhinaria on some of antennal segments. Apical rostral segment pointed or stiletto-shaped. Apterae have membranous dorsum, with numerous thick, rather short, fan-shaped or capitate hairs. Alatae have dark intersegmental sclerites and dusky marginal sclerites. Veins on forewings conspicuously dark-bordered. Siphunculi long and slender, sometimes slightly expanded at apex with small flange, Cauda finger-shaped, tongue shaped or triangular. Blackman (2010)
Plocamaphis feed low down on the stems or roots of willow (Salix). Not ant attended. Sometimes occur in mixed colonies with ant-attended species such as Tuberolachnus salignus.
Plocamaphis are rather large, sparsely hairy aphids, brown or yellowish brown; colour usually masked by dense flocculent wax. Antennae 6-segmented, rather more than half length of body. Rostrum rather long, reaching to about hind coxae. Abdominal dorsum of apterae without marginal sclerites, but dark spinopleural sclerites sometimes present. Marginal tubercles present on pronotum and tergites I-IV(V) Siphunculi clavate or vasiform without flange. Cauda tongue shaped, bearing 20-35 hairs. Related to Pterocomma but less hairy. Blackman (2010)
Feed on the evergreen shrub star anise (Illicium, Illiciaceae)
Apterae are medium-sized, Polytrichaphis fragilis is yellowish green, Polytrichaphis illicius is black. Antennal tubercles distinct, median frontal tubercle slightly developed. Antennae 6-segmented, longer than body; secondary rhinaria absent in aptera, present in alate on antennal segments III-V. First tarsal segments have 2,2,2 hairs. Media vein of alate forewing 2-branched, hind wing with 2 oblique veins, wing veins bordered with black bands. Siphunculi more or less cylindrical with distinct flange at apex. Cauda elongate tongue-shaped, not constricted. Miyazaki (1971),Qiao & Zhang (2001)
Pseudacaudella1 sp. Europe, Kazakhstan, Morocco, Brazil, USA, Panama, New Zealand
Only species, Pseudacaudella rubida, feeds on mosses.
Apterae very small, shiny olive green or brown. Head broad with very low antennal & median tubercles. Antennae short, 6-segmented, with terminal process longer than base antennal segment VI, & tapering to a point. Apterae with secondary rhinaria absent; present on alatae on III-IV or III-V. Hairs on body sparse, short & blunt. First tarsal segments all have 2 hairs. Forewings of alatae have media once-branched and veins dark bordered. Dorsum of aptera sclerotic, dark pigmented & mainly smooth. Siphunculi cylindrical, strongly imbricated with subapical constriction & large flange. Cauda short, with swollen basal part & narrow apical part, & bearing 4 hairs. Blackman (2010)
One species Pseudaphis abyssinica found on rose (Rosaceae) & grasses (Poaceae), suggesting host alternation; other 2 species found on flower heads of grasses. Ant attended on primary host.
Small to medium sized aphids, brown or green. Head without frontal tubercles, frons entirely flat. Antennae of apterae without secondary rhinaria; rhinaria on alatae present on antennal segment III. Spiracular pores on abdominal segment I & II very close together. Each abdominal segment with dorsal pigmented bar, on I-V entire or broken, on VI-VIII entire. Sclerite on VII fused with marginal sclerites to form large sclerite. Marginal tubercles sometimes present on segments II-IV. Siphunculi about as long as cauda, with only 1-5 rows of polygonal reticulations at apex. Related to Sitobion, but antennal tubercles absent. Hille Ris Lambers (1958),Aldryhim & Ilharco (1997)
Feed on crucifers (Brassicaceae), rolling the leaves of the host. Leaf rolls sometimes discoloured.
Apterae medium-sized, oval in shape, yellowish, brown or green, powdered with grey wax. Head without frontal tubercles, so frons more or less straight. Antennae 5 or 6-segmented, shorter than body, although terminal process relatively long. Secondary rhinaria absent on apterae, present on alatae on antennal segments III-V. Dorsal body hairs have blunt apices. First tarsal segments have 3,3,2 hairs. Apterae lack dorsal abdominal sclerotization; alatae have dark segmental cross-bands, sometimes fragmented. Siphunculi short truncate cones without flange. Cauda short, tongue shaped to triangular, with 5-6 hairs. Blackman (2010),Heie (1992)
Pseudocercidis rosae thought to be monoecious on rose (Rosa, Rosaceae), but possibly host alternating to lupin (Lupinus, Fabaceae); other species, Pseudocercidis tutigulus host alternating between Rosa and Corydalis (Papaveraceae)
Medium-sized, probably both species yellow-green covered in wax. Frontal tubercles well developed, smooth, with pointed hairs. Antennae 6-segmented, without secondary rhinaria in aptera. First tarsal segments bearing 5 or 6 hairs. Siphunculi short, not much longer than cauda, with well developed flange. Cauda short, triangular, not constricted near middle. Possibly related to Sitobion.Richards (1961)
Rather small, apterae usually green, pink or yellowish, with frosted appearance due to numerous pale fan-shaped dorsal hairs. Antennal and median frontal tubercles absent, so frons almost flat. Ocular tubercles rudimentary. Apical rostral segment typical stiletto-shape of aphids feeding on Anthemideae. Hairs blunt or fan-shaped. Marginal tubercles not evident. Wing venation as in genus Aphis. Siphunculi slender, slightly swollen distally on inner side, impinging against abdomen, and with thin-edged flange set obliquely. Cauda conical. Related to Epameibaphis,Flabellomicrosiphum and Coloradoa, but with characteristically-shaped siphunculi. Gillette & Palmer (1932)
Pseudomegoura magnoliae is polyphagous, feeding on plants in over 20 different families, including Citrus and various ornamental shrubs. Pseudomegoura nipponica mainly found on skunkvine (Paederia foetida, Rubiaceae), but also on Apocynaceae & Asteraceae. Mainly anholocyclic, but some holocyclic populations.
Apterae medium sized to rather large, yellowish red to pink or yellow-green, with front of head, part of siphunculi and cauda all dusky to dark. Siphunculi distinctly clavate. Cauda with only five hairs. Genus was synonomized with Aulacorthum, but using both molecular and morphometric analyses Lee et al. (2011) showed that A. magnoliae and A. nipponicum formed a clade that is not closely related to other Aulacorthum spp. They named the genus Neoaulacorthum, now synonomized with Pseudomegoura.Lee et al. (2011)
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Pterocomma43 spp. N hemisphere, 1 now in S America
Live on willows & poplars (Salicaceae). Monoecious holocyclic. Colonies on bark of branches and twigs are almost always attended by ants.
Rather large aphids, brownish, grey or blackish green with white, yellow or red siphunculi. Body is wax powdered, especially along segment borders, and is densely hairy, as are antennae and legs. Frons almost straight, sometimes with distinct median tubercle and very low antennal tubercles. Antennae about half as long as body, with terminal process usually longer than base antennal segment VI. Marginal tubercles usually well developed, present on prothorax & abdominal segments I-IV (VII). Siphunculi longer than wide, cylindrical or swollen with more or less distinct flange. Heie (1986)
Thought to be monoecious on rose (Rosa involucrata, Rosaceae)
Only species. Raychaudhuriaphis capitata, shares some characters with Chaetosiphon. Apterae are rather small & pale. Alatae unknown. Differs from Chaetosiphon in having spinulose head. Also has 3 hairs on first tarsal segments. Blackman & Eastop (1982-)
Only species, Rhinariaphis tuberculata, feeds on catmint (Nepeta (= Lophanthus) pinetorum, Lamiaceae)
Appearance in life unknown. Aptera has antennal tubercles well developed & divergent. Secondary rhinaria present on antennal segments III-V along entire length of each segment. Apical rostral segment has 24-40 accessory hairs. First tarsal segments have 3,3,3 hairs. Hairs on appendages long, thick and rigid with wide capitate apices. Abdominal dorsum wrinkled with large tubercles, wide at bases. Siphunculi clavate, narrower basal part clearly longer than swollen part and narrower than half of swollen part. Cauda is tongue shaped, not constricted, longer than its basal width. Genus has affinities to Eucarazzia and Klimazewskia.Kanturski & Stekolshchikov (2018)
Only species, Rhodobium porosum, feeds on rose (Rosa) and strawberry (Fragaria) spp. Monoecious holocyclic in North America, with sexuales occurring on both hosts. European populations often anholocyclic on cultivated roses in glasshouses.
Apterae medium sized, yellow to yellow-green, rather shiny, with brown head. Antennal tubercles well developed with inner faces spiculose & almost parallel; median tubercle also present. Apterae have secondary rhinaria on antennal segment III, alatae have them on III-IV or III-V. Hairs on dorsum and appendages very short. First tarsal segments have 3,3,3 hairs. Alatae have very dark wing veins. Dorsum of aptera slightly sclerotic, unpigmented. Alatae have dusky marginal sclerites. Siphunculi rather thick, tapering or cylindrical, without polygonal reticulation, and with flange. Cauda pale & finger-shaped. Blackman (2010)
Only species, Rhododendraphis tuatayae, feeds on Rhododendron.
Apterae medium-sized, colour in life unknown, probably brown or black. Head with low antennal tubercles and low or absent median tubercle. Antennae 6-segmented, shorter than body, with short terminal process. Antennal segment III bears a few secondary rhinaria. Rostrum long reaching to hind coxae, with apical rostral segment bearing many hairs. First and second tarsal segments spinulose. First tarsal segments have 3,3,3 hairs. Tergum dark and sclerotic with dark bands on tergites VII & VIII. Hairs on dorsum short with capitate apices. Siphunculi clavate, swollen on distal half, with scaly pattern before flange. Cauda short, tongue-shaped, not constricted, with small number of hairs. Barjadze & Ozdemir (2014)
Rhopalomyzus9 spp. N Hemisphere, 1 now in S America
Aphids host alternate between honeysuckle (Lonicera, Caprifoliaceae) and grasses (Poaceae). Holocyclic, overwintering as eggs on honeysuckle.
Medium-sized yellowish to black aphids. Head has small but distinct antennal tubercles, and usually median tubercle. Antennae 6-segmented, slightly shorter or same length as body, with long terminal process. Apterae without secondary rhinaria, alatae have numerous rhinaria on segments III-IV or III-V. Dorsal cuticle of apterae may have dark cross bands on posterior tergites; alatae have dark crossbands often fused into large dark abdominal patch. Marginal tubercles frequently present on the prothorax and abdominal segments II-VI. Siphunculi swollen with a small, but well developed flange, slightly constricted just under flange. Cauda tongue-shaped or triangular, and shorter than siphunculi. Blackman (2010)
Rhopalosiphoninus20 spp. Mainly Asia, also Europe, N America, 2 worldwide
Live on great variety of plants, including Lamiaceae, Rosaceae, Iridaceae, Araliaceae and Grossulariaceae. Often live in cryptic habitats near the ground. Some species host alternate, some stay all year on one host.
Medium sized aphids, usually dark & shiny. Head cuticle spiculose, with well developed antennal tubercles, inner faces parallel of converging; median tubercle undeveloped. Antennae about as long as body, with long terminal process. Apterae may or may not have secondary rhinaria, alatae have them on III, III-IV or rarely III-V. Dorsal hairs usually short & blunt. First tarsal segments have 3,3,3 or 3,3,2 hairs. Dorsal cuticle of aptera may be membranous or completely sclerotic; alatae often have black dorsal shield. Apart from constriction near apex, apical two thirds of siphunculi are strongly and sharply swollen, apical part before flange with reticulate sculpturing. Cauda short, tongue-shaped or triangular. Blackman (2010)
Only species, Richardsaphis canadensis, thought to be monoecious holocyclic on shrubby cinquefoil (Dasiphora fruticosa = Potentilla fruticosa, Asteraceae)
Small to medium-sized, spindle-shaped, pale green to yellow aphids with rather short appendages. Antennae only 0.33 x body length, and without secondary rhinaria; terminal process shorter than base of antennal segment VI. Head has low antennal tubercles and rounded median tubercle. Rostrum short, not reaching to middle coxae; apical rostral segment oblong triangular with blunt apices. First tarsal segments all have 2 ventral hairs. Dorsal body hairs blunt and somewhat capitate. Dorsum sclerotic and wrinkled. Cauda has spinulose imbrications. Siphunculi rather long, with distal part often slightly swollen, and with small, but distinct flange. Cauda tongue-shaped. Kanturski et al. (2018)
Only species, Roepkea marchali, has mahaleb cherry (Prunus mahaleb, Rosaceae) as primary host and various mints in Lamiaceae such as hemp-nettles (Galeopsis) & woundworts (Stachys) as secondary hosts.
Apterae medium sized, varying in colour from almost black to greenish to orange-yellow. Apterae on primary host have antennal and median frontal tubercles poorly developed. Antennae 6-segmented, without secondary rhinaria. Rostrum reaches almost to hind coxae. Prothorax and abdomen are without marginal tubercles. First tarsal segments each have 2 or 3 hairs. Cauda short, and bluntly triangular. Resemble aphids in genus Nearctaphis, but lack marginal, abdominal, and prothoracic tubercles usually present on aphids in that genus. Richards (1969)
Only species, Rostratusaphis rhododendronitos, feeds in colonies on young branches of Rhododendron simsii (Ericaceae). Life cycle unknown.
Apterae are small to medium-sized, black in life with dark siphunculi & some wax powder. Antennal tubercles poorly developed. Antennae 6-segmented, shorter than body, with short terminal process; apterae without secondary rhinaria, alatae with few on antennal segments III-IV. Rostrum very long, ultimate rostral segment long wedge-shaped with numerous accessory hairs. First tarsal segments have 3,3,3 hairs. Dorsum sclerotized, dark brown and smooth. Dorsal hairs short and pointed. Abdominal segments III-V with small marginal tubercles. Siphunculi long cylindrical, slightly inflated in middle, constricted under well developed flange. Cauda cone with 4-6 long fine hairs. Differs from Ericaphis and Ericolophium, by the length of terminal process, and number of accessory hairs on apical rostral segment. Fang & Qiao (2009)
Rubiaphis altica feeds singly on the undersides of leaves along veins of its host raspberry (Rubus idaeus, Rosaceae). Life cycle unknown.
Apterae medium-sized, without sclerotization, & semitransparent. Well developed antennal & median tubercles. Antennae 5-segmented, without secondary rhinaria. Apical rostral segment elongated wedge-shaped with straight sides. Hairs on head and dorsum very long, hairs on antennae short. First tarsal segments have 3,2,2 or 3,3,2 hairs. Small marginal tubercles present only on the prothorax; spinal tubercles absent. Distance between centres of spiracles on abdominal segments II and III much less than twice distance between centres of spiracles on segments I and II which are well separated. Siphunculi relatively long, without any trace of polygonal reticulation. Cauda elongated triangular with widely rounded apex. Proximity of spiracles on abdominal segments II and III would normally indicate Aphidini, but absence of marginal tubercles on abdomen & shape of siphunculi & cauda indicate Macrosiphini. Rubiaphis most closely related to Myzaphis.Stekolshchikov & Novgorodova (2020)
A small genus with pear (Pyrus, Rosaceae) as primary host, roots of Artemisia as secondary host.
Apterae medium-sized, white, yellowish, red or brown. At least one species covered with white woolly wax. Antennae short with a few indistinct secondary rhinaria on segment III; alate vivipara has secondary rhinaria on III & IV. Number of hairs on first tarsal segments 3,3,2. Long hairs on body and antennae. Dorsum is unmarked; in alate abdomen with dark dorsal abdominal cross-bars. Cauda broader than long. Related to Dysaphis but distinguished by long hairs. Matsumura (1918)
Only species, Scleromyzus corylopsis, feeds on witch hazel (Corylopsis, Hamamelidaceae). Life cycle unknown.
Apterae medium-sized. Colour in life not recorded. Head without median frontal tubercle, antennal tubercles very weakly developed. Sparse spinules in region of antennal tubercles. Antennae 6-segmented, slightly longer than body; secondary rhinaria absent. Rostrum reaches beyond hind coxae, with apical rostral segment broad and stout. Dorsum of abdomen rugose, pale but with spino-pleural sclerites on tergites I & II, scattered sclerites on IV & V, and postsiphuncular sclerites. Siphunculi almost cylindrical and longer than cauda, which is elongated, much darker than siphunculi and bears 5-6 hairs. Immatures have strongly spinulose femora and smooth hind tibiae. Spinulose head suggests Myzus, but this aphid has weakly-developed antennal tubercles and post-siphuncular sclerites. Basu et al (1976)
Semiaphis17 spp. N hemisphere, incl. N Africa (2 spp.)
Some Semiaphis have honeysuckle (Lonicera, Caprifoliaceae) as primary host and Asteraceae as secondary hosts. Others are monoecious on Lonicera or Asteraceae. Two species have moved to Impatiens (Balsaminaceae).
Medium-sized, usually greenish aphids, & usually lightly wax powdered. Median and antennal tubercles present, but weakly developed. Antennae 6-segmented (rarely 5-) and about half body length. Secondary rhinaria usually absent in apterous females; present on antennal segments III & IV of alatae. No dark dorsal patch in either apterae or alatae, with abdominal dorsum membranous apart from dark cross bands on posterior tergites. Marginal tubercles occasionally present on abdominal segments II-V. Siphunculi about half body length, shorter than cauda, without flange, and positioned between abdominal segments V and VI. Cauda tongue shaped or triangular with 5-7 hairs. Blackman (2010)
Shinjia1 sp. E India, Nepal, China, Korea, E Siberia, Japan, Philippines, Australia
Shinjia orientalis feeds on young growth of Viburnum spp. in spring, secondary hosts are several species of ferns. Probably anholocyclic on ferns in Australia.
Apterae medium-sized, shining yellow with black antennae and dark tips to siphunculi; alatae have paired brown patches partially fused across midline. Head without spinules. Antennal tubercles short, with a distinct median tubercle. Eyes without distinct ocular tubercles. Antennae 6-segmented, without secondary sensoria in apterae; terminal process is long. long. Wing veins normal, hindwings a little reduced in size, often with one oblique vein. Trochanters defined from the femora; tarsi are rudimentary, minute, without claws. Dorsum scarcely corrugated in apterous form, with short hairs. Siphunculi long, very slightly swollen, not reticulated. Cauda elongate. Mastopoda pteridis has similar vestigial tarsi and also feeds on ferns, but not closely related. Takahashi (1938)
Sinomegoura7 spp. E&S Asia, 1 also in Australia & California
Feed on various trees and shrubs in E and south-east Asia, including Lauraceae, Rutaceae, Rubiaceae, Ericaceae. Life cycles generally unknown, some species probably anholocyclic.
Apterae medium or rather large, reddish, yellowish or greenish with dark tipped siphunculi. Similar to Megoura, but head has spinules on antennal tubercles and ventrally. Also body reticulated on dorsum of thorax and abdomen. Marginal sclerites of abdomen not developed. Siphunculi weakly swollen, calf-shaped. Cauda long. Takahashi (1960)
Sitobion81 spp. orig N hemisphere, some in Africa S of Sahara
Some species alternate from Rosaceae to grasses (Poaceae), but most remain on grasses all year where may or may not have sexual stage. At least one species is serious pest of cereals.
Medium-sized to rather large spindle-shaped green to dull brownish-green or reddish-brown aphids, with blackish antennae. Antennal tubercles low, median tubercle not well developed. Antennae of apterae usually with 1-4 secondary rhinaria on segment III; alatae have them on III or III-V, but never numerous. Antennal hairs usually very short. Typically have intersegmental sclerotic pattern, but some species have a brownish sclerotic tergum. Siphunculi rather long, blackish, sclerotic, with apical part reticulated and small but distinct flange. Cauda pale, elongate and finger-shaped. Similar to Macrosiphum, but that genus has longer antennal hairs. Blackman (2010)
Monoecious holocyclic on crucifers (Berteroa, Alyssum, Erysimum, Brassicaceae). Usually colonising terminal parts of shoots, deforming leaves and flower buds.
Rather small with oval body and long thick hairs, green or blackish, usually covered in dense white wax powder. Antennal tubercles low with median frontal tubercle. Apterae usually have secondary rhinaria on antennal segment III. First tarsal segments have 2,2,2 hairs. Marginal tubercles on prothorax & abdominal segments I-V are very small. Siphunculi dark, broad, volcano-shaped, shorter in length than width at base. Cauda short. Related to Brevicoryne.Shaposhnikov (1950)
Sorbaphis1 sp. Japan, Korea, China, E&W Siberia, S Urals
Only species, Sorbaphis chaetosiphon, has primary host as Sorbus (Rosaceae), secondary host as leopard plant (Ligularia spp., Asteraceae). Spring colonies curl leaves of Sorbus spp. downward and turn them reddish. On secondary host live in ant shelters at stem base.
Emigrant alatae have shining black abdomen; apterae on secondary host medium sized, grey brown to blackish. Characterised by having 8-15 very long, thin hairs of the basal half of siphunculi, with similar hairs on body and antennae. First tarsal segments have 4:4:2 hairs. The spiracles are broadly oval, located in posterior part of the large oblong plates. There are no spinal or marginal tubercles. Shaposhnikov (1950)
Monoecious holocyclic on various Brassicaceae (Alyssum, Berteroa)
Apterae are small, greyish green with slight wax cover. Head with weak antennal tubercles and broad frontal median tubercle. Antennae reaching at most 0.5 x body length, with terminal process longer than antennal segment VI. Apterae without secondary rhinaria; alatae have rhinaria on segments III & IV. Apical rostral segment pointed triangular with 4 pointed bristles. First tarsal segments with 3,3,2 hairs. Abdominal dorsum without central sclerite, but with marginal sclerites, ante-and postsiphuncular sclerites and transverse bands posterior to siphunculi. Related to North American Landisaphis, but with different hairs on first tarsal segments, and without the development of the spinal sclerites on abdominal tergites 6-8 into rugose processes. Heinze (1960)
Staegeriella necopinata feeds on bedstraws (Galium), possibly Coprosma and/or woodruff (Asperula) (all in Rubiaceae).
Rather small greyish-green oval aphids, with very low divergent antennal tubercles. Antennae much shorter than body, with terminal process about twice as long as base of last segment. Apterae without secondary rhinaria, alatae have rhinaria on antennal segments III or III-IV. First tarsal segments usually have 2,2,2 hairs. Dorsal body hairs very short. Dorsal body cuticle membranous apart from dusky transverse bars on abdominal tergites VII & VIII; alatae have pale marginal sclerites & dorsal cross bands on posterior tergites. Siphunculi truncate, shorter than cauda. Cauda tongue- or finger-shaped. Blackman (2010)
Most Staticobium species are monoecious holocyclic on sea lavender (Limonium, Plumbaginaceae). Not visited by ants.
Apterae medium-sized, usually reddish brown or dark brown. In both apterae and alatae antennal tubercles are broad, low and smooth. Antennae have relatively long terminal process with a few rhinaria on segment III. Spiracular apertures covered by cowl-like opercula, an adaptation to regular immersion. Siphunculi more or less cylindrical, tapering, sclerotic and pigmented with reticulation below a small flange. Similar to Macrosiphoniella, but antesiphuncular sclerites are absent. Also similar to Sitobion aphids, but dorsum not completely sclerotic, pleurospinal sclerites are absent from the alate and the reticulate area on the siphunculus is larger than in Sitobion.Blackman (2010)
Only species, Stellariopsis songini is monoecious holocyclic on stitchwort (Stellaria dichotoma, Caryophyllaceae). It feeds on stems and undersides of leaves.
Apterae are medium-sized, elongate oval, pale green, lightly dusted with wax. Antennal tubercles barely indicated, with well developed median tubercle. Antennae 6-segmented, shorter than body, without secondary rhinaria; alatae have rhinaria on III-IV (V). Apical rostral segment long, with numerous hairs. First tarsal segments have 3,3,3 hairs. Dorsal hairs sit on broad, strongly raised tubercles. Tergum in aptera sclerotic, in alate membranous without central sclerite. Siphunculi long, conical, with distinct flanges; shorter than elongated triangular cauda. Possibly related to Spatulophorus, but differs in more numerous body hairs arising from tubercles, short conical siphunculi and rather hairy apical rostral segment and cauda. Szelegiewicz. (1969)
Only species, Subacyrthosiphon cryptobium, is monoecious holocyclic, feeding on older parts of prostrate stems of white clover (Trifolium repens, Fabaceae). Shows cryptic behavior, drop when disturbed, and not attended by ants.
Antennal tubercles well developed, median tubercle undeveloped. Antennae of both apterae & alatae have only few secondary rhinaria on the basal part of antennal segment III. Hairs on dorsum & antennae short & blunt. First tarsal segments have 3,3,3 hairs. Apterae have dark antesiphuncular and postsiphuncular sclerites; alatae also have marginal sclerites. Spiracular apertures small & partially covered by opercula. Siphunculi long, broad-based, cylindrical, with distinct flange. Cauda tongue-shaped to triangular with 6-8 hairs, the apical ones having spear-shaped apices. Blackman (2010)
Only species, Subovatomyzus leucosceptri, in monoecious on several genera of Lamiaceae including beautyberry (Callicarpa), Colebrookea, and Vietnamese balm (Elsholtzia). Sexuales do not appear to have been described.
Apterae medium sized, spindle-shaped, pale translucent green with darker green spinal stripe, and whitish appendages. Antennal tubercles well developed; median tubercle lower, but still pronounced. Antennae of apterae without secondary rhinaria; in alatae numerous rhinaria on antennal segments III-V. Number of hairs on first tarsal segments 3,3,3. Tergum of aptera pale & membranous with very short, sometimes capitate hairs like those on antennae. Alate has dark central abdominal patch. Siphunculi distally swollen, with distinct preapical circumcision below small flange. Cauda with constriction at base, occasionally in middle. Differs from Ovatomyzus in having distinct median tubercle, and lacking long hairs on antennal tubercles. Resembles Capitophorus in having short capitate dorsal hairs and smooth clavate siphunculi. Basu (1964)
Most feed on Saxifragaceae or ferns (Polypodiopsida).
Rather small or medium sized aphids, shining black or pale yellow or brown. There is dorsal spiculation on the head. Antennal tubercles well developed, with inside faces nearly parallel. Apterae have secondary rhinaria on antennal segment III (-IV); alatae have them on segments III-V. Antennal terminal process is longer than antennal segment III. Body sclerotized on thoracic and abdominal segments. Siphunculi swollen below distal half, minutely spinulose, with large flange with incomplete reticulation below it. Cauda elongate with hairs below constriction. Alate (?) has 4 incomplete transverse sclerites before siphunculi, and postsiphuncular sclerites are present. Related to Utamphorophora, but distinguished by spiculation. Tao (1963)
Only species, Tauricaphis arabisi feeds on mountain rockcress (Arabis caucasica, Brassicaceae). Monoecious holocyclic.
Apterae are rather small, greenish with mainly yellowish brown appendages. Related to Lipamyzodes, but distinguished by apterae having secondary rhinaria on antennal segment III & dorsal abdominal hairs arising from tubercles. Blackman & Eastop (1982-)
Tenuilongiaphis stata feeds on Chinese mugwort (Artemisia argyi, Asteraceae) (secondary host ?). Primary host thought to be sea buckthorn (Hippophae rhamonoides, Elaeagnaceae). Very sedentary.
Apterae medium sized, pale green, with two longitudinal rows of darker green spots. Body elongate with numerous short dorsal cylindrical processes. Head without prominent antennal tubercles. Antennae with 4-5 antennal segments, shorter than 0.25 x body length. Apical rostral segment much longer than second hind rostral segment. Dorsal body hairs rather elongate, thick and pointed. Siphunculi stout, cylindrical, bent at base & without flange. Cauda short & tongue-shaped. Differs from other genera in the Macrosiphini in having very short antennae, numerous dorsal processes, and lack of flange on siphunculus. Zhang & Zhong (1994)
Only species, Thalictrophorus thalictrophilus feeds on columbine meadow-rue (Thalictrum aquilegifolium, Ranunculaceae). Life cycle unknown.
Apterae medium-sized, white in life. Antennal tubercles indistinct, median tubercle absent. Antennae 6-segmented, 0.55 x body length, with terminal process about twice base of antennal segment VI. Rostrum reaching abdominal segment I. Number of hairs on first tarsal segment 4,4,4. Siphunculi long, barrel shaped, slightly elongated at base, flange distinct, 1.33 x cauda. Cauda short, nearly triangular-shaped, constricted at media, bearing only 5-6 hairs. Perhaps related to Longicaudus but that has unusually long cauda; similar to Lipaphis, but that genus has fewer tarsal hairs 3,3,3 or 3,3,2. Zhang & Qiao (2000)
Monoecious holocyclic on wormwood (Artemisia, Asteraceae). Very mobile, rarely occurring in colonies. At least 1 species attended by ants.
Apterae medium-sized to rather large, green or brown, with long dark siphunculi. Antennal tubercles not well developed, front always distinctly concave. Antennae at least as long as body, with long terminal process. Apterae have secondary rhinaria on antennal segment III. Rostrum long reaching beyond hind coxae. First tarsal segments have 3,3,3 hairs. Dorsal hairs blunt. Marginal sclerites absent from apterae. Siphunculi extremely long, nearly half as long as body, without reticulation and without flange. Cauda with numerous hairs. Resembles Macrosiphoniella, but that genus has siphunculi with reticulation. Heie (1995),Hille Ris Lambers (1947)
Apterae medium-sized, whitish, pale yellow or yellowish. Antennal tubercles divergent, not high. Median frontal tubercle conspicuous. Antennae with 6 segments, shorter than body. There are tubercular spinal processes on abdominal segments VII & VIII, resembling supracaudal process in Cavariella. Alatae have quadrate black dorsal abdominal patch, and secondary rhinaria on antennal segments III-IV (V). Immatures have spinulose hind tibiae. Resembles Liosomaphis, but that genus has no tubercular spinal processes, nor spinulose hind tibiae. Narzikulov (1957)
Trichosiphonaphis9 spp. W Europe to E Asia, 1 now also worldwide
Aphids typically host alternate between primary host honeysuckle (Lonicera, Caprifoliaceae) & secondary host knotweed (Polygonum, Polygonaceae).
Rather small to medium-sized aphids, blackish, green, yellow or brown. Head spiculose, with variably developed antennal tubercles. Antennae of apterae lack secondary rhinaria, alatae have them on segments III-IV. Alatae do not have a dark dorsal abdominal patch. The 3 Trichosiphonaphis s. str. spp. have hairs on the siphunculi (hence genus name), and siphunculi have distinct apical flange; the 7-9 spp. in subgenus Xenomyzus spp. may or may not have hairs on siphunculi, and siphunculi are flangeless. Cauda is short, usually with more than 7 hairs. Blackman (2010)
Copyright Laszlo Ersek all rights reserved
Tshernovaia2 spp. Siberia, Transbaikalia, Russia, Mongolia, Korea
Only 2 species in genus. Tshernovaia adenophorae feed on ladybells (Adenophora, Campanulaceae) and also sweet wormwood (Artemisia annua). Lives in ant-attended colonies. Tshernovaia spirocaudicula feed on 'bluebells' (Campanulaceae) and wormwood (Artemisia).
Medium-sized aphids, one species dull black, the other yellow, both with dark antennae and siphunculi. Antennal tubercles low, median tubercle undeveloped. Antennae about as long as body, with long terminal process. Apterae have secondary rhinaria on antennal segment III (IV). Apical rostral segment conical with numerous basal hairs. There are 5,5,5 hairs on first tarsal segments. Siphunculi nearly cylindrical, with distinct flange and distal part reticulated. Cauda distinctive - triangular base with few hairs, and long, narrow, hairless distal part. Anal plate with large process bearing many long hairs. Genus close to American Bipersona, but differ in structure of cauda. Holman & Szelegiewicz (1964)
Only 2 species in genus, both monoecious holocyclic. Tubaphis ranunculina live on buttercups (Ranunculus) and Tubaphis clematophila on clematis (Clematis), both in Ranunculaceae.
Small pale spindle-shaped aphids. Apterae have fairly well developed, widely separated antennal tubercles. Antennae are as long as body or longer, with unusually thin basal part to last segment. Hairs on dorsal body and antennae are very short & blunt; dorsal cuticle is wrinkled. Siphunculi cylindrical, thin but with broader base and with constriction below apical flange. Cauda short, tongue shaped, has distinctive constriction at base and bears 4 hairs. Alatae do not have dark abdominal patch, but do have numerous secondary rhinaria on antennal segment III, & few on IV-V. Blackman (2010)
Single species in genus, Tuberoaphis hydrangeae, has only been found on Hydrangea aspera (Hydrangeaceae). However, since it appears to be related to Macromyzus, may have ferns as secondary host. Tuberoaphis hydrangeae ssp. digitata could be second species.
Apterae rather small, yellowish or whitish with apices of appendages darker. Head with prominent antennal tubercles, slightly diverging. Antennae 6-segmented, a little shorter than body length, without secondary rhinaria. Eyes without distinct ocular tubercles. Abdominal dorsum corrugated, and with prominent finger-like tubercles: 8 pairs spinal, 5 pairs marginal. Siphunculi cylindrical, imbricated, expanded at base and much longer than cauda. Cauda small, subconical. Anal plate rounded. Tseng & Tao (1938)
Live in galls on primary host plum (Prunus, Rosaceae) in spring, later migrating to secondary host Artemisia, Chrysanthemum (Anthemidae, Asteraceae) on growing points (subgenus Tuberocephalus) or on subterranean parts (subgenus Trichosiphoniella).
Apterae rather small to rather large, greenish or yellowish aphids. Dorsum of head with spinules. Antennal tubercles finger-shaped or round. Antennae 5- or 6-segmented, shorter than body, aptera without secondary rhinaria. Rostrum short. Number of hairs on first tarsal segment 3,3,2 or 3,3,3. Siphunculi cylindrical, imbricated, with apex gradually tapering, with or without hairs. Cauda usually triangular with 4-6 hairs. Alatae have protruding, not very high antennal tubercles, secondary rhinaria on antennal segments III-IV(V), and often spino-pleural bands on the abdominal tergites. Two subgenera of Tuberocephalus are distinct in apterae on secondary host: Tuberocephalus sstr. have Phorodon like head; Trichosiphoniella have Myzus like head. Su et al. (2010),Tao (1963)
Tumoranuraphis1 sp. Uttar Pradesh, India, NW China
Only species, Tumoranuraphis indica, feeds on Himalayan bird cherry (Prunus cornuta, Rosaceae) within folded leaf pseudogall. Heteroecious holocyclic, but secondary host unknown.
Apterae on primary host are large, yellow-green covered with grey powdery wax, with brown siphunculi. Frontal tubercles are very low or indistinct. Antennae are about 0.72 x body length, with terminal process about 4 x base of antennal segment VI. Secondary rhinaria are absent in the aptera; numerous on antennal segment IV (?) of alatae. Number of hairs on first tarsal segments is 5,5,5. Distance between spiracles on tergites II & III is 1.7-1.9 x distance between those on tergites I & II. Siphunculi are about 0.41 x body length, clavate with widest part about 3 x apical width. Cauda semicircular with 19-23 hairs. Zhang et al. (1999)
Only 2 species recognised, Turanoleucon mitjaevi & Turanoleucon jashenkoi, both feeding on stems of thistles (Cousinia, Echinops in Cardueae, Asteraceae). Not visited by ants.
Apterae rather large, blackish, with cuticle largely reticulated. Antennal tubercles low & divergent, median frontal tubercle large, similar to antennal ones. Antennae 6-segmented, shorter than body, with terminal process 3-4 x base of antennal segment VI. Protruberant secondary rhinaria on segment III in both apterae and alatae. Rostrum very long, reaching abdominal sternite IV, with fine elongated apical rostral segment. First tarsal segments with 5,5,5 hairs. Dorsal hairs thick, developed on large sclerites. Ante- & postsiphuncular sclerites absent. Large process on anal plate. Siphunculi cylindrical, with reticulation on 0.35-0.45 of length, and distinct flanges. Cauda finger-shaped with rounded apex. Similar to Macrosiphoniella, but has 5 hairs on first tarsal segments and large median frontal tubercle. Resembles Uroleucon, but has no ante- or post-siphuncular sclerites. Kadyrbekov. (2002).
Ucrimyzus villalobosi forms dense colonies on stems of plants in various genera (Bidens, Schkuhria, Senecio, Stevia) of the daisy family (Asteraceae). Life cycle unknown.
Apterae medium-sized, pale dull green, with yellowish antennae & legs. Antennal tubercles divergent & low, but bigger than median tubercle. Antennae 0.93-1.28 x body, with terminal process 5.3-8.2 x base of antennal segment VI. Secondary rhinaria on antennal segment III in apterae, & III-V in alate. Rostrum reaching hind coxae, with triangular apical rostral segment. Prothoracic spiracular apertures rounded & only slightly wider than those on abdomen. First tarsal segments have 3,3,3 hairs. Abdomen membranous with few small unpigmented sclerites. Siphunculi asymmetrically swollen, 1.4-1.7 x cauda. Cauda lanceolate, with 5-7 fine, curved, pointed hairs. Resembles Capitophorus, but has smaller prothoracic spiracles than that genus. Durante & Hidalgo (2013)
Only species, Uhlmannia singularis is monoecious holocyclic on woodruff (Asperula), bedstraw (Galium) and Cruciata (all in Rubiaceae).
Apterae are medium sized, dark grey, almost black, covered with white wax powder. Forehead convex without antennal tubercles. Antennae 6-segmented, with terminal process over 1.5 longer than base of segment VI Apterae without secondary rhinaria; alatae only have rhinaria on segment III. Abdominal dorsum membranous, finely wrinkled. Pleural bristles present from mesothoracic segment to abdominal segment V. Abdominal tergite VIII covers cauda like a hood, with cone-shaped projection. Siphunculi shorter than basal width, curved, with opening shifted backwards and without flange. Cauda triangular with more than 8 hairs. Heinze (1960)
Uroleucon250 spp. N&S America, Europe, Asia, Africa, 2 now in Australia
Uroleucon aphids feed almost exclusively on daisies (Asteraceae) and bellflowers (Campanulaceae). They do not host alternate, and usually have sexual stage in life cycle. Few species may be ant attended.
Aptera rather large, shiny red, brown, bronze or green with black siphunculi. Antennal tubercles well developed & divergent, median tubercle undeveloped. Antennae 6-segmented with secondary rhinaria on segment III in both apterae & alatae. First tarsal segments usually have 5,5,5 hairs, few have 3,3,3. Dorsal hairs are neither thick nor distinctly capitate, usually placed on dark scleroites. Apterae & alatae usually have dark postsiphuncular sclerites. Siphunculi rather long, much longer than cauda, with zone of polygonal reticulation occupying distal 0.15-0.4 of length, and small flange. Cauda long and finger-shaped. Blackman (2010)
Mainly feed on Rosaceae and/or grasses (Poaceae); ancestor probably host alternated between two. Not ant attended.
Medium to large apterae, rather pale green or yellow. Antennal tubercles moderately developed, inner sides parallel or diverging. Antennae about as long as body or longer, with long terminal process. Apterae with or without secondary rhinaria, alatae have them on III or III-IV. Antennal & dorsal hairs very short & blunt. Apical rostral segment is short & blunt. First tarsal segments have 3,3,3 hairs. Dorsal cuticle of apterae unmarked; alatae have black dorsal markings. Siphunculi rather long & more or less swollen. Cauda elongate, constricted near middle. Blackman (2010)
Host alternate between Ericaceae (Rhododendron, Lyonia) and sedges (Carex, Cyperaceae), or monoecious on Ericaceae or Cyperaceae.
Rather small, oval or spindle shaped aphids. Antennal tubercles poorly developed but, in apterae of some species, anterior part of head has roundish processes between antennal bases. Antennae 5- or 6-segmented, shorter than body, with terminal process about as long as base of antennal segment VI. Apterae without secondary rhinaria, but alatae have them on antennal segments III-V. Hairs on dorsal body and appendages mostly very short and pointed. First tarsal segments have 3,3,2 hairs. Media of forewing has one or two forks. Siphunculi either cylindrical or with distal half swollen, squamous and strongly constricted at apex. Abdominal segment VIII partly covers cauda. Cauda tongue-shaped, with constriction between swollen basal part and narrower distal part. Blackman (2010)
Only species, Vietaphis aliquanti, feeds on fern Plagiogyria japonica. Aphids form loose colonies on undersides of fronds. Life cycle unknown.
Apterae rather small, body yellowish green with antennal segments III-VI dark, legs pale and siphunculi dark tipped. Antennal tubercles developed, parallel or slightly diverging. Antennae 6-segmented, shorter than body length; antennal segment III in apterae without secondary rhinaria, but present in alatae on segments III-V. First tarsal segments with 3,3,3 hairs. Hind tibiae of nymphs without spinules. Dorsum of head near eyes with C-shaped wrinkles, dorsum of abdomen with C or O-shaped wrinkles; alatae with dark dorsal patch on abdomen. Marginal tubercles on abdomen absent. Siphunculi cylindrical with dense imbrications, not constricted under developed flange. Cauda cone shaped, distal half slightly constricted with 5 hairs present. Su et al. (2014)
Monoecious holocyclic on campions (Silene, Viscaria, Caryophyllaceae). Usually distort & discolor plant.
Apterae medium-sized, pale green or yellow-green, some with white wax powder. Antennal tubercles very low with granulate cuticle. Antennae shorter than body, with terminal process about 3 x base of antennal segment VI. Both apterae & alatae have secondary rhinaria on the distal part of antennal segment III. Femora scaly. First tarsal segments with 2, 3, or 4 hairs. Alate without dark dorsal patch. Siphunculi slightly swollen, with little developed flange. Cauda rather long, tongue-shaped or triangular. Closely related to Aphidura but without mesosternal tubercles. Heie (1994)
Wahlgreniella6 spp. Europe, N America, Russia, (E Asia?), 1 sp. worldwide
Most species live on plants of heather family (Ericaceae); do not host alternate, except perhaps Wahlgreniella nervata which may alternate between Rosa and Arbutus (Ericaceae). Not ant attended.
Apterae rather large, green or yellow. Antennal tubercles well developed with diverging or parallel inner sides. Antennae rather long and thin, with very long terminal process; apterae have few secondary rhinaria on antennal segment III, alatae have them on III or III-IV. Hairs on antennae and body dorsum short & blunt. First tarsal segments have 3,3,3 hairs. Dorsal abdomen membranous in apterae, with dark sclerotized markings in alatae. Siphunculi long and swollen with no reticulation and distinct flange. Cauda tongue shaped with 5 hairs. Similar to Amphorophora, but have fewer caudal hairs. Blackman (2010)
Primary host of both species is Stachyurus (Stachyuraceae). Secondary host of Xenosiphonaphis conandri is rock tobacco (Conandron ramondioides, Gesneriaceae). Secondary host of Xenosiphonaphis japonica unknown.
Aptera of 1 species rather large, other species very small. Colour of aphids not recorded. Antennal tubercles very broad. No median tubercle. Antennae 6-segmented, little shorter than body, with terminal process less than 3 x base of segment VI; segment III is without secondary rhinaria. Hind tibiae with short hairs, with spinules in immature stages. Abdomen without distinct dorsal and marginal sclerites and tubercles. Siphunculi longer than cauda, roughly imbricated, with some minute spinules, obliquely truncated and without flange at tip. Cauda stout, longer than wide. Immature alatae of X. japonica are densely covered with cottony wax. Very similar to Jacksonia, but in that genus first instars are without spinules on hind tibiae. Takahashi (1961)
Zinia1 sp. Urals, Russia, Moldova, Kazakhstan, Poland, Italy
Only species, Zinia veronicae, feeds on roots of speedwell (Veronica, Asteraceae). Not ant attended.
Adult apterae medium sized, pale green, with dark grey shiny dorsum, black antennae and siphunculi. Frons slightly convex, antennal tubercles low and diverging. Antennae 6-segmented, reaching beyond siphunculi, with secondary rhinaria on segment III. Rostrum reaches hind coxae. First tarsal segments have 3,3,3 hairs. Dorsum covered with dark sclerotic shield with irregular boundary from segments I-VI. Marginal tubercles on pro-and metathorax, and abdominal segments I-VII. Spinal tubercles present on head, pronotum and segments VII & VII, often on other tergites. Siphunculi cylindrical, with distinct flange at apex. Cauda rounded, slightly flattened, as long as wide. Species combines some characters of Dysaphis and Brachycaudus.Shaposhnikov (1950)
Parachaitophorus spiraeae, feeds on meadowsweet (Spiraea, Rosaceae). Ant-attended. Disappearance in late May indicates migration to unknown secondary host.
Apterae rather small with dark brown spots at bases of long stout dorsal bristles, & dark siphunculi & cauda. Antennal tubercles absent. Eyes small, triommatidia in fundatrices and oviparae. Antennae 6-segmented, much shorter than body, without secondary rhinaria. Apterae have much shorter terminal process than alatae. Dorsal hairs arise from dark tuberculate bases. Siphunculi short, conical with flange at apex. Cauda elongate, rounded at apex & constricted. Related to Patchia, but differs in elongate cauda & dorsal hairs arising from tubercles. Takahashi (1937)
Most Betacallis species are recorded from birches (Betulaceae), although one species (Betacallis prunicola) has apparently become associated with plums (Prunus, Rosaceae).
All viviparae alate. Rather large, greenish. Head short, with characteristic transverse dark bar on head ventrally between the eyes, extending to prothorax. Antennae much longer than body, secondary rhinaria on segment III. Rostrum reaches nearly to middle coxae. Pterostigma long & lanceolate, stigma vein strongly curved, first oblique vein robust. Siphunculi long, nearly 3 x as long as broad, distinctly constricted at middle, & somewhat trumpet-shaped at apex. Cauda long, nearly twice as long as broad, and constricted near base. Hannabura and Illinoia species on Alnus do not have transverse dark bar on head. Matsumura (1919)
Betulaphis5 spp. Holarctic including Iceland & Greenland, 1 now in New Zealand
Feed on undersides of birch leaves (Betula, Betulaceae). Monoecious holocyclic. Not attended by ants.
Small, rather flat oval aphids. Adult viviparae winged or wingless. Frontal tubercles barely evident. Short 6-segmented antennae without obvious hairs. Secondary rhinaria narrowly oval, extending half way round circumference. Body with few hairs, capitate in aptera. Siphunculi with broad base, tapering, very short, with apical flange. Cauda short & conical. Anal plate bilobed. Oviparae have dark dorsal markings & posterior abdomen is extended as egg-laying organ. Glendenning (1926)
Boernerina5 spp. W Siberia to Japan, Alaska, Canada
Monoecious holocyclic on alder (Alnus, Duschekia, Betulaceae). Apterae apply themselves closely to leaf surface.
Apterae dorso-ventrally flattened, rather elongate oval. Head usually has paired anteriorly-directed rectangular projections. Antennae 5-segmented. Marginal abdominal hairs arising from asymmetric tubercles which give abdominal margin a stepped appearance. Alatae are more normal-looking Calaphidini. One species (B. occidentalis) in subgenus Boernerinella because apterae often have 6-segmented antennae, frontal projections are only weakly developed and abdominal margin is more indented than stepped. Also apterae have dark sclerotic bars on abdominal dorsum; alatae have bars both dorsally & ventrally, together with numerous wax glands (see picture). Hille Ris Lambers & Hottes (1962)
Calaphis14 spp. N hemisphere, 1 now in S Africa, Australia & NZ
All except one live on birch (Betula, Betulaceae). Monoecious holocyclic. Not usually attended by ants.
In some species all viviparae are alate; others have both apterous & alate viviparae. Delicate pale-coloured aphids with rather long thin legs. Antennal tubercles well-developed. Antennae longer than body, with terminal process longer than base. Secondary rhinaria present on antennal segment III in all morphs. Sometimes have distinctive markings and/or dark wing veins; radial sector in forewing absent or indistinct. First tarsal segments have 5 ventral & 2 dorsal hairs. Siphunculi low, truncate with extended apertures. Cauda slightly constricted. Anal plate bilobed in viviparae. Heie (1982)
Callipterinella3 spp. Europe to Japan, 1 now in N America
All species live on birch (Betula, Betulaceae), either on leaves or growing shoots. Monoecious holocyclic. Colonies may be dispersed or aggregated. Usually attended by ants.
Small to medium-sized. Viviparae may be winged or wingless. Very variable in colour from green to brown, yellow or reddish, commonly with brown vertex to head and other dark dorsal markings. Antennae shorter than body; terminal process longer than base segment VI. Secondary rhinaria on segment III in alatae. Radial sector indistinct or absent; other wing veins dark bordered. Body covered with long strong hairs. Siphunculi dark with rows of minute spinules. Cauda constricted and knobbed. Heie (1982)
Monoecious holocyclic on birch (Betula, Betulaceae). Feeding habits distinctive in that all species tend to be solitary, or only live in small groups; very active, dropping when disturbed.
Rather large aphids, coloured green or greenish yellow with siphunculi either wholly or apically black. Viviparae may be winged or wingless. Antennal tubercles prominent. Vertex and antennae with short capitate hairs. Antennae longer than body, with terminal process longer than base of antennal segment VI; antennal segment III with secondary rhinaria. Fore wing with veins heavy and somewhat bordered; smoky at tip. Radial sector present or absent. Siphunculi short, truncate, imbricated. Cauda spatulate, long, with evident neck and long basal portion. Anal plate moderately cleft. Treated by Blackman as a subgenus of Calaphis.Granovsky (1928)
Live on twigs and young branches of alder (Alnus) and birch (Betula) (both Betulaceae). Monoecious holocyclic. May be attended by ants.
Large hairy brown aphids. All adult viviparae and males are winged; ovipara is wingless. Antennae shorter than the body. Abdominal dorsum has pigmentation confined to marginal sclerites plus a few bands. Also bands of light wax pulverulence on abdomen. Siphunculi are short and truncate, and the cauda is knobbed. Heie (1982)
Only species, Crypturaphis grassii, lives on the leaves of Italian alder (Alnus cordata, Betulaceae). Monoecious holocyclic. Not attended by ants.
Wingless females are dorsoventrally flattened. Have pair of prominent projections on both head and prothorax. Antennae shorter than the body, with only 3 segments. Eyes without distinct ocular tubercles. Siphunculi rudimentary. Cauda scarcely constricted; anal plate slightly indented. Apterae resemble coccids rather than aphids. Alatae have a more typical 'aphid appearance'. Takahashi (1938)
Euceraphis11 spp. N America, Europe to E Asia, 1 now in N America, Australia & New Zealand
Live on birch (Betula and alder (Alnus) (both Betulaceae). Adults may be found as accidentals on many plants besides true hosts. Monoecious holocyclic. One species considered pest of ornamental birch varieties.
Rather large active but fragile aphids with long thin legs. All adults apart from oviparae are winged. Secrete a bluish white wax, often in the form of tufts on their legs. Antennae usually longer than the body. May have black dorsal abdominal markings. Cauda knobbed & anal plate rounded. Oviparae large, apterous, yellowish to dark brown with dark dorsal abdominal markings, and with the posterior abdominal segments extended into ovipositor-like structure. Stroyan (1977)
Both species feed on alder (Alnus, Betulaceae). Monoecious holocyclic.
Rather small whitish or yellowish spindle-shaped aphids. Antennae much longer than the body length, with antennal segment VI much the longest. No antennal tubercles, but inner side of antennal segment I has projection. On the frontal margin of head there are numerous tubercles each of which bear long capitate hair. Thorax & abdomen have similar hair-bearing tubercles. First tarsal segments with 5 ventral hairs. Siphunculi of aptera short, but distinctly longer than basal diameter, with apical constriction; siphunculi much longer in alatae. Cauda is small and rounded; genital plate with 6 long tubercles, each bearing long, broad capitate hair.
Genus Hannabura related to Calaphis, but Hannabura species have fewer hairs on the first tarsal segment. Matsumura (1917)
Only species, Latgerina orizabaensis, is monoecious holocyclic on alder Alnus acuminata, Alnus firmifolia, Betulaceae).
Apterae are medium-sized, flattened dorsoventrally, & coloured pale yellow with black antennae. Alatae have black head, thorax and appendages and black dorsal abdominal markings. Antennae 6-segmented, with protuberance on segment I; terminal process slightly widened at apex. Rostrum has sclerotized basal collar. Body provided with tridigitate processes, each finger of which bears a long spine. Processes are distributed around body: 1 anterior frontal pair, 2 marginal pairs on pronotum & mesonotum, 1 marginal pair on metanotum & on each of abdominal tergites I-VIII. Siphunculi short, widened into cone at base, inserted on tergite VI. Cauda with slight constriction. Remaudiere (1981)
Monaphis1 sp. Europe, to E. Siberia, China, Japan, USA
Only species, Monaphis antennata, is monoecious holocyclic on birch (Betula, Betulaceae). Not attended by ants.
All viviparae alate. Rather large, ventrally flattened, green aphids. Frons has prominent antennal tubercles, higher than median tubercle. Antennae very long, and conspicuously blackish; terminal process also very long, up to 9 x base segment VI. Antennal segment III bears many secondary rhinaria. Rostrum short, not reaching middle coxae; apical rostral segment blunt, with up to 6 subsidiary hairs. Wings with normal venation, with long, narrow, dark pterostigma. Abdomen membranous. Tergites III-VI with marginal tubercles. Siphunculi very small, pale, truncate conical with a flanged rim. Cauda rounded, broadly tongue-shaped or blunt conical, with about 10-12 hairs. Stroyan (1977)
Feed on undersides of leaves of birch (Betula) or alder (Alnus) (both Betulaceae). Monoecious holocyclic. Not attended by ants.
Apterae rather small to medium-sized, pale yellow or yellowish-green. Head spinulose, without antennal tubercles, but with distinct median tubercle. Antennae 6-segmented, with terminal process shorter than base segment VI. Apterae without secondary rhinaria; rhinaria present on segment III in alate. First tarsal segments with 5 hairs. Tergum of aptera distinctly segmented, sclerotic, with some dorsal hairs quite long, knobbed on conical bases. Siphunculi truncated, conical with wide flange. Cauda elongated with very distinct constriction at about basal third, and a nearly acute tip with many hairs. Anal plate bilobed. Basu (1964),Qiao & Zhang (2002)
Only species, Oestlundiella flava, in monoecious holocyclic, feeding on undersides of leaves of alder (Alnus, Betulaceae), & tending to form small aggregations.
All viviparae are alate. Alatae are rather large, delicate, lemon yellow with plumes of bluish white wax on antennae and legs. Antennae on distinct, diverging antennal tubercles. Antennae 6-segmented, somewhat longer than the body, with secondary rhinaria. Forewing of alate has media vein twice branched, and pterostigmal vein present, not deeply curved. Siphunculi truncate, constricted in middle, placed on broad swollen bases. Cauda elongated, cord-shaped & knobbed in spear-like fashion, with constriction near distal half. Anal plate distinctly and broadly, but not deeply, bilobed. Both cauda and anal plate are hairy. Related to Euceraphis, but they have siphunculi much longer than wide, not placed on swollen base. Granovsky (1930)
Only species, Platyaphis fagi, is monoecious holocyclic on Japanese beech (Fagus crenata, Fagaceae). Lives on undersides of leaves, along mid-ribs. Life cycle unknown.
Apterae moderately sized, broadly ovate, flattened, green with pale antennae and legs. Without wax pores.
Head fused with prothorax; other thoracic segments & all abdominal segments also fused. Thoracic and first 7 abdominal segments each produced laterally into pointed lobes, with pointed hair at tip. Antennae short, concealed under head, 4-segmented, and without secondary rhinaria. Rostrum very short, 3-segmented. Legs concealed under body. First tarsal segments with 2 hairs. Siphunculi reduced to minute rings. Cauda small, short, rounded, concealed under body. May be related to Dasyaphis or Hormaphis.Takahashi (1957)
Monoecious holocyclic, on twigs of birch (Betula) and alder (Alnus) (both Betulaceae). Usually always attended by ants.
All viviparae alate or brachypterous. Alatae are rather large shiny dark brown aphids. Antennae 6-segmented, stout, shorter than body, with short terminal process; segment III with protuberant secondary rhinaria. Antennal hairs numerous. Rostrum reaching about to middle coxae, with apical segment blunt. Wings with veins brownish-bordered. First tarsal joints with 6-10 ventral and 0-2 dorsal hairs. Dorsum has transverse spinopleural bands & marginal sclerites on each tergite. Siphunculi, when present, small and truncate, situated on marginal sclerite. Cauda and anal plate both broadly rounded. Brachypterous apterae similar to alatae except that wings, pterothorax, ocelli, secondary rhinaria and sclerotic pattern are reduced. Stroyan (1977)
Robust aphids, living solitary on leaves of alder (Alnus) and birch (Betula) (both Betulaceae). Probably monoecious holocyclic.
Apterae rather large robust aphids, alatae have darker legs & antennae, and dark-tipped siphunculi.
Frontal tubercles well developed. Antenna 6-segmented, longer than the body, with short terminal process. Secondary rhinaria present in aptera. Rastral organ well developed on all tibiae. First tarsal segments with 5-7 ventral hairs, without dorsal hairs. Dorsal abdominal hairs long, blunt, or weakly capitate. Marginal tubercles present. Siphunculi with swollen bases & strongly flared apically, in the alate siphunculi bent outwards. Cauda with elongate, tongue-shaped knob. Anal plate moderately indented. Wax gland pores on appendages. Quednau (1973)
Two species feeding on chestnut (Castanea) & oak (Quercus) (both Fagaceae), one species on bog myrtle (Myrica gale, Myricaceae). Monoecious holocyclic. Recently re-established as genus for these species
All viviparae alate. Alatae are yellow or orange. Characterized by brown median line on vertex and pronotum, and usually paired black spinal and marginal sclerites. Pronotum of alate often bears more than one pair of marginal hairs. Wing veins are bordered, and decorated with a triangular spot. Cocuzza et al. (2023)
Single species in genus, Andorracallis pujadei, has only been caught in traps, so host unknown. Until 2023 considered a subgenus of Myzocallis.
Vertex, sclerotic parts of body, tibiae & antennae have minute wax pores. Base of antennal segment VI with 1 hair. Antennal & dorsal body hairs blunt, shorter than 0.5 x basal diameter of antennal segment III. Subcostal vein without hairs. 1 pair of abdominal marginal hairs per tergite. Tergite VIII with 4 hairs. Quednau (1999)
Only species, Apulicallis trojanae, feeds on leaves of Macedonian oak (Quercus trojana, Fagaceae). Monoecious holocyclic.
Alatae are medium sized, lemon yellow, with head & thorax very slightly brownish. In all morphs there is 1 pair of spinal hairs on each abdominal tergite. In alate vivipara, lobes of mesonotum smooth. Wings hyaline and tibiae not marked with black. Marginal abdominal tubercles developed on tergites III & IV. Siphunculi without connection to marginal sclerite VI. Quednau (1999)
Hoplocallis4 spp. Europe to India, 1 now in S America
All species live on oak (Quercus, Fagaceae). Where known monoecious holocyclic.
Small aphids, pale green or yellow with dark markings. All adult viviparae are winged. Antennal terminal process always shorter than base of antennal segment VI. Head and prothorax have median longitudinal pale stripe extending backward from median ocellus between bands of pigment. Pronotum has anterior and posterior spinal and marginal clusters of small hairs. Abdomen has paired dark spinal sclerites that are fused posteriorly across midline on some or all tergites. Distinguished from Myzocallis by short terminal process. Quednau (1999)
Only species, Hoplochaetaphis zachvatkini, feeds on oak (Quercus, Fagaceae). Adapted to living in leaf rolls. Probably monoecious holocyclic. May mimic caterpillar faeces.
Apterae are rather small, broadly pear-shaped, reddish, orange or dull brown, with dark dorsal sclerotic pattern. Sometimes dusted with thin mealy wax. Antennae 6 segmented, no more than 0.5 x body length, with terminal process about equal base antennal segment VI. Antennae & body covered with very long fine hairs; on dorsum they sit in groups of 1-5 hairs on dark sclerites which often merge into symmetrical spots. First tarsal segments have 5 hairs. Siphunculi stump-shaped obliquely cut at apex & without hairs. Cauda small, broad & flask shaped. Alatae have paired dark patches or cross-bands on abdominal tergites III-VII. Aizenberg (1959),Quednau (1999)
Feed on various Nearctic oak (Quercus, Fagaceae) species. Live on leaves in dense colonies.
Apterae have antennal tubercles undeveloped. Antennae 6-segmented, with short terminal process. Secondary rhinaria present in aptera on antennal segment III. Rostrum 4-segmented with short triangular apical segment. Head, thorax & abdomen have prominent, long, thick spines over tuberculate dorsum; alatae have much shorter, spine-like hairs. Aptera bears small indistinct or large paired rectangular patches on each abdominal tergite; on alatae each tergite has small median pigmented patch on each side, as well as marginal sclerites. Siphunculi short, smooth, without hairs, and with no apical flange. Cauda knobbed, anal plate weakly bilobed. Possibly related to Chaitophorus given pigmented spiny dorsal hairs, or to Neosymydobius.Granovsky (1933),Quednau (1999)
Monoecious, holocyclic on terminal twigs of red oak (Quercus, Fagaceae) saplings. Live in small compact colonies on young bark & petioles of leaves. Well attended by ants.
Apterae medium-sized, shiny dark brown to black, covered with many stiff hairs. Antennae 6-segmented, shorter than body, with long, bristle-like hairs. Terminal process very short and thick. Apterous viviparae without secondary rhinaria, but alatae have large round rhinaria. Antennal tubercles undeveloped. Rostrum 4-segmented, with apical segment subconical. Prothorax and abdomen usually without spinal or marginal tubercles. Wings with broad fuscous bands bordering rather heavy veins. Terga of aptera fused forming sclerotic carapace; alatae with pigmented sclerites. Siphunculi truncate, very short, not as long as wide, without flange. Cauda broadly rounded, semicircular, & not knobbed; anal plate indented. Anal plate & cauda profusely armed with long bristle-like hairs. Granovsky (1933),Quednau (1999)
Lineomyzocallis17 spp. Panama to Canada, 1 now in Europe & W Asia
All species monoecious holocyclic on various different Nearctic species of oak (Quercus, Fagaceae). Until 2023 considered a subgenus of Myzocallis.
In alate morph sides of pro- & mesonotum have black band extending from edge to base of hind wings; costal margin of both wings usually with black band over costal field extending well past stigma to wing apex. Pterostigma mostly elongate. Apices of wing veins without dark triangular spots. Lobes of mesonotum smooth. At least apical halves of fore tibiae or all tibiae black. First tarsal segments with 5 (rarely 3 or 4) hairs. Siphunculi always pale. Quednau (1999),Cocuzza et al. (2023)
Live on undersides of leaves of oak (Quercus, Fagaceae). Life cycle unknown. Adult apterae appear to diapause on underside of old leaf, only reproducing when new leaves appear.
Apterae very small. Antennae have 4- or 5-segmented antennae. Triommatidia not very distinct from other facets of eye. Base of second segment of rostrum often weakly sclerotized. First tarsal segments have only 2 or 3 ventral hairs. Has long thick spiculose spinal and marginal hairs. Cauda has a reticulated zone on lower face of its basal part. Lobes of anal plate fused at base by elongated and pigmented sclerite. Winged vivipara unknown. Remaudiere 1982,Quednau & Remaudiere (1995)
Myzocallis17 spp.Europe to W Asia? a few now near WW
Most species feed on oak (Quercus & chestnut (Castanea) (Fagaceae); few on Betulaceae. They have a sexual stage in the life cycle, but do not host alternate and are not attended by ants.
Small, delicate, usually yellowish aphids with a knobbed cauda and bilobed anal plate. Immatures usually have long, capitate dorsal hairs. Vertex always without brown median band. Vertex with 2 or 3 pairs of posterior discal hairs. Pronotum only with 1 pair of marginal hairs. Wing veins not edged and without diffuse apical spot. Siphunculi pale or darkened. Quednau (1999)
Mainly monoecious holocyclic on oak (Quercus, Fagaceae), 1 species on milkweed (Asclepias, Apocynaceae). Until 2023 considered a subgenus of Myzocallis.
Alatae medium sized, most yellowish or pinkish with irregular pattern of markings. Vertex pale or pigmented, if pigmented then without narrow pale median line. Fore wings with radial sector complete. Anterior lobes of pronotum usually spiculose. Abdomen with spinal pairs of low tubercles on tergites, or finger-like processes on tergites I & II, & with pairs of roundish spinal & marginal sclerites, which together with intersegmental sclerites, make a large perforated blotch over tergites IV & V. Siphunculi densely covered with spicules. Quednau (1999)
Monoecious holocyclic on oak (Quercus, Fagaceae). Attended by ants.
Apterae medium-sized, usually brownish in colour with banded antennae. Median frontal & antennal tubercles undeveloped. Secondary rhinaria on antennal segment III round, on half or more of segment. Forewing veins not fuscous bordered, or only faintly so. Abdomen has 0-5 marginal tubercles. Siphunculi short and truncate. Cauda rounded to weakly knobbed, & anal plate bilobed. Resemble Symydobius, but are not closely related to them. Similar appearance appears to result from convergent evolution, both feeding on bark of terminal twigs and being ant attended. Quednau (1999)
Monoecious on oak (Quercus, Fagaceae). Some species known to be holocyclic, but Pasekia cocciferina thought to have anholocyclic populations. Feed on undersides of leaves. Until 2023 considered a subgenus of Myzocallis.
Where colour in life known, alatae have head & thorax brown, and abdomen mostly yellowish, often with dark dorsal markings. Antennal flagellum spiculose. Base of segment VI with 1 hair near primary rhinarium. Primary rhinarium often elongate. Pterostigma rather short & broad. Spinal abdominal sclerites usually large. Siphunculi not incorporated in marginal sclerite VI, even if sclerotic. Aizenberg (1959),Quednau (1999)
Patchia1 sp. Florida, North Carolina, Pennsylvania, Virginia, USA
Only species, Patchia virginiana, feeds on bark of chestnut (Castanea, Fagaceae). Monoecious holocyclic.
Apterae medium sized, broadly oval, rather uniformly velvety-black; alate viviparae brown with a large black dorsal abdominal patch and thickly-bordered forewing veins. Both morphs secreting wax. Apterae have separate head and prothorax. Antennae 6-segmented, hairy with circular secondary rhinaria in alate. Fore wing has media twice branched, the radial sector absent or faintly indicated; hind wings with both cubital veins present. Siphunculi truncate. Cauda rounded or slightly conical. Anal plate divided into two parts. Possibly related to Lachnochaitophorus.Baker (1920)
Only species, Serratocallis takahashii, feeds on twigs, leaf petioles and undersides of leaves of oak (Quercus, Fagaceae). Life cycle unknown.
Apterae medium sized, brown. Alatae have short, broad pterostigma with black spot at base. Antennae 6-segmented, shorter than body, with short terminal process. Secondary rhinaria absent in apterae, present in alatae. Abdominal terga with transverse pigmented sclerotic bars, irregularly broken. Dorsal body hairs some thin & hair like, other stout and spine-like on tuberculate bases. Siphunculi truncate. Cauda tongue-shaped, without constriction. Anal plate bilobed. Related to Hoplochaetaphis but dorsal hairs differ. Quednau & Chakrabarti (1976),Quednau (1999)
Only species, Siculaphis vittoriensis, feeds on oak (Quercus, Fagaceae). Some populations holocyclic, others thought to be anholocyclic. Forms ant-attended colonies along mid-ribs on basal parts of undersides of leaves.
Apterae rather small, pale yellowish green with longitudinal olive green dorsal stripes. Vertex almost fused with anterior sclerites of pronotum. Antennae 6-segmented, shorter than body, with more than 3 hairs on each of segments I-II. Apterae usually without secondary rhinaria on segment III; alate with rhinaria on segment III-V. First tarsal segments with 0-1 dorsal hairs. Dorsal body hairs with incrassate bifurcate apices. Abdomen with segmentally separated pairs of spinal and marginal sclerotic plates usually with darker border and paler centre. Siphunculi truncate, with tendency to fuse with marginal sclerite VI. Cauda tongue-shaped without constriction; anal plate bilobate. Quednau & Barbagallo (1991)
Feed on oak (Quercus) and chestnut (Castanea) (Fagaceae). Monoecious holocyclic, not attended by ants.
All viviparae are winged. Alatae mostly medium sized, greenish or yellowish. Frontal tubercles poorly developed. Antennae as long as, or longer than body; terminal process a little shorter, similar to, or longer than base of antennal segment VI. Antennal segment III has rather broad oval secondary rhinaria. First tarsal segments with 5-6 ventral & 2 dorsal hairs. Fore coxae a little larger than middle & hind coxae. Abdomen with dorsal & marginal tubercles. Siphunculi short, truncate & smooth. Cauda knobbed. Anal plate bilobed. Immatures have long capitate hairs. Richards (1965)
Only species, Wanyucallis amblyopappos, feeds on oak (Quercus liaotungensis, Fagaceae).
Only apterae known. Frontal tubercles poorly developed. Antennae 6-segmented, 0.6 x body length, with terminal process more or less equal to base segment VI. With or without secondary rhinaria on segment III. First tarsal segments with 5 ventral & 0-2 dorsal hairs. Metanotum & abdomen with mutually free pairs of large spinal sclerites; on tergites I-V sclerites bulging, spiculose and bearing stout hairs. Marginal & pleural sclerites also present. Siphunculi weakly sclerotic, cylindrical, not merging with marginal sclerite VI, & with apical flange. Cauda triangular, without constriction, & with membranous bladder-like apex. Anal plate moderately bilobed. Similar to Hoplochaitophorus, but distinguished by bulging spinal sclerites. Quednau (1999)
Chromaphis2 spp. India to China, 1 also in N&S America & Europe
Feed on undersides of leaves of walnut (Juglans, Juglandaceae). Monoecious holocyclic. Not attended by ants.
All viviparae winged. Alatae rather small, pale yellow. Antennae shorter than body, with terminal process much shorter than base segment VI; segment III with oval secondary rhinaria. Antennal hairs short. Fore coxae somewhat enlarged. First tarsal segments usually with 7 hairs. In autumn small pairs of spinal spots on abdominal tergites IV-V. Siphunculi truncate conical without flange. Cauda knobbed. Anal plate slightly emarginate. Immatures with long capitate hairs. Heie (1982)
Only species, Chuansicallis chengtuensis feeds on Chinese sumac (Rhus chinensis, Anacardiaceae) & hardy rosewood (Dalbergia hupeana, Fabaceae) (possibly also Phyllanthus emblica, (Euphorbiaceae)
All adult viviparae alate. Alatae medium-sized, green, secreting profuse cottony wax threads. when at rest the wings put horizontally on the abdomen. Head of alate with median longitudinal suture. Antennal tubercles not well developed. Antenna 6 segmented, with terminal process more or less equal to base segment VI; segment III bears very long, slit-like secondary rhinaria. Body without tubercles. Siphunculi truncate, longer than wide. Cauda knobbed. Anal plate bilobed. Distinguished from other known genera by having suture on head. Life cycle unclear, but sexuales are known. Tao (1964),Quednau (2003)
Ctenocallis3 spp. Europe, W Asia, 1 also in N America
Feed on broom (Cytisus, Genista, Calicotome, Fabaceae). Monoecious holocyclic
Adult viviparae winged or wingless. Apterae medium-sized aphids, yellowish or brown. Antennae shorter than body, with terminal process shorter than base segment VI; secondary rhinaria transverse oval, present in all morphs. Body of aptera bears long finger-like, marginal, backwardly directing processes; alate has much reduced processes. Siphunculi pore-like, situated at the base of the marginal processes on tergite VI. Cauda knobbed. Anal plate bilobed in viviparae. Stroyan (1977)
Eucallipterus2 spp. Europe, SW&C Asia, N Africa, now in N America, New Zealand
Feed on undersides of leaves of lime (Tilia, Malvaceae). Monoecious holocyclic. Not attended by ants.
All viviparae winged. Active, delicate, medium-sized aphids with long thin legs. Antennae about as long as body, with terminal process shorter than base segment VI; segment III has transverse oval, rather narrow secondary rhinaria. Antennal hairs short. Wings have conspicuous dark spots. Fore coxae considerably enlarged. First tarsal segments have 5-7 hairs. Siphunculi truncate. Cauda knobbed. Anal plate bilobed. Heie (1982)
Monellia5 spp. N America, now in S America, Mediterranean
All feed on various species of hickory (Carya, Juglandaceae). Monoecious holocyclic. Monellia native to North America, but Monellia caryella invasive as pecan pest to South America, southern Europe and Middle East.
All viviparae winged. Alatae medium-sized, with yellow flattened body. Antennal tubercles slight, but there are two pair of tubercles, one directed forward in front of antenna, and one directed backward and sideways. Antennae about 0.75 x body, with secondary rhinaria on segment III. Wings held horizontal at rest. Abdomen has large rough marginal extensions on segments I-III. Siphunculi hemispherical, opening somewhat anteriorly, & with one curved hair on posterior edge. All hairs pointed. Legs have fore coxae greatly enlarged. Cauda is knobbed, & anal plate bilobed with numerous hairs. Resembles Monelliopsis, but probably closer to lime tree feeding groups such as Eucallipterus and Tiliaphis.Quednau (2003)
Monelliopsis10 spp. N America, 2 now in Europe, Africa
Feed on walnuts (Juglans) and/or pecan trees (Carya) (both Juglandaceae). Native to North America, but at least two species invasive in Europe, Asia or Africa.
All viviparae winged. Alatae rather small or medium sized, yellowish. Vivipara has frontal tubercles poorly developed. Hairs on head sometimes on wart-like processes. Antennae are six segmented, with terminal process a little shorter or longer than base antennal segment VI. Secondary rhinaria on segment III. In some species thoracic segments have spinal hairs on wartlike elevations. Wings held upright at rest. Forecoxae greatly enlarged. Dorsal hairs on anterior tergites often on mammiform processes. Marginal tubercles on tergites I-V. Siphunculi nearly poriform, with marginal hair of tergite VI on or near posterior margin. Cauda knobbed, anal plate bilobate. One obvious distinction between Monelliopsis and Monellia species is that latter lay wings flat. Quednau (2003)
Neocranaphis2 spp. West Bengal, India, China, Taiwan
Feed on bamboos (Arundinaria (Pleioblastus) or Bambusa) in the Poaceae). One species,
Neocranaphis bambusicola, known to produce sexuales.
All viviparae alate. Medium-sized to large, elongate-bodied, white, dusky on thorax, without dorsal abdominal markings, secreting cottony wax. Eyes with ocular tubercles. Rostrum short reaching just beyond fore coxae. Bristle-like empodial hairs present. Dorsal body hairs surrounded by many wax gland pores developed as cribriform discs, on abdomen not on sclerites. Veins in fore wings clear cut or weakly bordered. Radial sector obliterated at apex. Siphunculi poriform. Related to Shivaphis & Phyllaphoides.Quednau (2003)
Feed on walnut (Juglandaceae) typically along midrib of upper surface of leaves. Monoecious holocyclic. Not attended by ants. May be serious pest on walnuts.
All viviparous females are winged. Large distinctive yellow aphids with short antennae only about 0.3-0.4 x the body length; long conspicuous hairs on segment III. The wings have the veins dark bordered with dark spots near the wing margin. The abdomen has dark marginal sclerites, broad dark bands across tergites III-VII, broken ones across tergites I-II and small trapezoid sclerite on tergite VIII. Siphunculi dark sclerotic, short, truncate and without flange. Cauda has elongate oval knob, anal plate deeply incised. Quednau (2003)
Only species in genus, Phyllaphoides bambusicola, feeds on bamboo (Bambusa, Phyllostachys, Poaceae). Populations may be holocyclic or anholocyclic.
Apterae rare or absent. Alate viviparae medium-sized, white with pale yellow mesothorax, & oblong body secreting white cottony wax. Eyes are prominent, but lack ocular tubercles. Antennal tubercles absent. Antennae 6-segmented, about as long as the body, with the terminal process about as long as base antennal segment VI. Round secondary rhinaria. Rostrum rather short. Wings hyaline, media vein twice forked, hind wings with 2 oblique veins. Tarsi without empodial hairs. Body without prominent hairs. Siphunculi very short, much wider than long, scarcely more than pores. Cauda globular, constricted at the base. Anal plate bilobed. Quednau (2003)
Monoecious on hickory (Carya, Juglandaceae). Live on upper surface of the leaf, usually along midribs of basal leaflets. Sexuales found for 3 species, so likely that all species are holocyclic.
All adult viviparae alate. Alatae medium sized to rather large, yellow or yellow-orange. Antennal tubercles undeveloped. Antennae 6-segmented, with terminal process about 0.5 x base segment VI. Median and paired ocelli prominent. Wings have thicker than usual cubital veins. Forecoxae enlarged. Thorax & abdomen bear prominent hair-bearing tubercles on anterior segments. Spinal tubercles of abdominal segments much larger than those on each side. Siphunculi rounded, pore-like, about as large as ocular tubercle. Cauda knobbed. Anal plate bilobed. Immatures have tubercles bearing thick fan-shaped hairs prominent on all segments. Related to Monelliopsis but that has terminal process similar in length to base antennal segment VI. Bissell (1978),Quednau (2003)
Feed on leaves of lime (Tilia, Tiliaceae). Monoecious holocyclic.
All adult viviparae alate. Alatae medium sized to rather large, green, yellow or white with dark brown markings on wing and sometimes on body, black antennal bases & pale siphunculi. Antennae as long as body, with secondary rhinaria on segment III; terminal process about 1.5 x base segment VI. Media of forewing only once branched, with a very short radial sector. Abdomen without distinct spinal tubercles, but short blunt marginal tubercles present. Siphunculi longer than wide at middle, expanded at base, truncated & smooth. Cauda much constricted at base, globular, but with rounded protuberance on venter, with several hairs. Takahashi (1961),Quednau (2003)
Only species, Pseudochromaphis coreana, is monoecious on members of Ulmaceae, especially thorn elm (Hemiptelea davidii) and Siberian elm (Ulmus pumila). Populations are holocyclic.
Alatae rather small, pale greenish yellow, with forewings extensively mottled with dark pigment, and characteristic dark markings on abdominal dorsum. Median frontal tubercle is distinctly produced. Antennae about 0.7 x body length. Media vein on forewing is twice branched, & radial sector absent. Abdomen has dark spinal, pleural and marginal patches, with hairs placed on small tubercles. Siphunculi truncate, about 0.7 x as long as diameter of base. Cauda knobbed. Most likely related to Sinochaitophorus.Zhang & Zhong (1982)
Feed on young shoots & undersides of leaves of Japanese elm (Ulmus japonica) & Ulmus pumila (both Ulmaceae). Monoecious holocyclic. Attended by ants.
Apterae rather small, blackish; alatae blackish brown mottled with red, with maculate wings. Head and prothorax fused together; abdominal tergites I-V also fused to form carapace. Frontal tubercles undeveloped. Antennae about 0.5 x body length. Siphunculi cylindrical with poorly developed flange. Cauda is knobbed. Differs from Hoplochaitophorus in having the head and prothorax fused together. Takahashi (1938),Quednau (2003)
Feed on Pteryocarya & Juglans (Juglandaceae). Monoecious holocyclic.
Apterae are rather small, dorso-ventrally flattened, pale yellowish green. In aptera & nymphs, body has conspicuous sausage-shaped processes, bearing spiculose dorsal body hairs. Head & prothorax fused together. Compound eyes small without ocular tubercle. Antennae only 3-segmented in apterae, 5-segmented in alatae. Second hind tarsal segments with only 2 ventral hairs. Siphunculi minute, poriform. Takahashi (1938),Quednau (2003)
Mesocallis aphids mostly feed on trees in the birch family (Betulaceae) including birch (Betula), hornbeam (Carpinus), alder (Alnus) and hazel (Corylus). One species reported from beech (Fagaceae). Monoecious holocyclic.
Pale yellow, slender-bodied aphids, with both alate & apterous morphs known in some species. Antennae much shorter than body, with terminal process about same length as base segment VI; secondary rhinaria present on segment III. Rostrum reaches far beyond first coxae. Abdomen is without spinal processes, and paramedian hairs are mostly on wart-like elevations. In both apterae & alatae dorsal body hairs have round knobs at apex. Empodial hairs flabellate and distinctly longer than claws. Fore tibiae often darkened. Siphunculi pale and truncated without a flange. Cauda knobbed & anal plate bilobed. Quednau (2003)
Monoecious on twigs and branches of Betulaceae. Attended by ants.
All viviparae alate. Head produced at front above median ocellus. Without frontal tubercles. Antennae 6-segmented, much shorter than body, with very short terminal process; secondary rhinaria present only on segment III. Fore wings with large dark markings. Body stout, with many long hairs scattered on abdominal dorsum arising from small warts. Marginal pigmented sclerites of abdomen well developed; few small tubercles on some segments anterior to siphunculi; dorsal sclerotized bands sometimes present on anterior abdominal segments. Siphunculi short truncated. Cauda constricted at base, globular. Anal plate bilobed. Takahashi (1961)
Pterocallis14 spp. N hemisphere, 1 now in S America
Feed on alder (Alnus) & hazel (Corylus) in Betulaceae. Monoecious holocyclic. Usually dispersed on undersides of leaves. Few species attended by ants, most not.
Both apterous & alate viviparae present. Small pale aphids. Antennae usually somewhat shorter than the body with short terminal process; secondary rhinaria usually absent from apterae, present on segment III in alatae. Fore coxae slightly enlarged. First tarsal segments with 5 ventral & 0-2 dorsal hairs. Adult apterae & immatures with numerous long, blunt or capitate dorsal hairs. Abdomen without spinal processes. Marginal tubercles present on pronotum and abdominal segments, divided into small wax-producing facets. Siphunculi short & truncated. Cauda knobbed. Stroyan (1977)
Feed on sedges (Cyperaceae). All species are monoecious holocyclic. Not attended by ants.
Medium sized aphids, oval or pear-shaped bodies. Aptera usually has dorsal abdominal pattern of pigmented blackish areas. Alatae have more-or-less regular series of dark bands on tergites III to VIII, those on III-VI often as a central shield. Forewings have dark-bordered veins & dark areas along distal parts of veins. Dorsal hairs usually short and fan-shaped, with no mushroom-shaped hairs. Dorsum is without membranous borders from mesonotum to abdominal tergite I, and from tergites III or IV to VI. Siphunculi stump-shaped with rounded apical rim, apparently between segments V & VI. Diagnostic characteristics vary in relation to environmental factors. Richards (1971),Quednau (2010)
Only species, Juncobia leegei, feeds on rushes (Juncus, Cyperaceae). Monoecious holocyclic. Attended by ants.
Apterae medium-sized, yellowish with blackish grey markings. Head rounded with sides sloping from antennal socket to anterior margin of eye. Antennae rather strong, with segments adorned with rings of spicules; terminal process very short. apical rostral segment spiculose on dorsal side. Dorsal hairs all fan-shaped & without tuberculate bases. Siphunculi short cones, situated between tergites V & VI. Tergite VIII without processes. Quednau (2010)
Feed on sedges (Carex, Cyperaceae). Monoecious holocyclic.
Medium-sized, yellowish or brownish. Aptera has extensive sclerotization consisting of dark head, pair of large blotches over mesonotum until tergite I, another pair over tergites III-VI, and dark tergite VIII. Alatae have bordered wing veins. Head broad, with 2 rod-like or spatulate hairs. Accessory rhinaria on antennal segment VI placed close to the primary rhinarium. Basal dorsal hairs on tibia inconspicuous (not modified). First tarsal segments have 5 hairs. Dorsal body hairs almost exclusively very short & mushroom shaped (except on tergite VIII). Dorsum with tuberculate hair bases. Siphunculi situated on tergite VI. Near to Iziphya but differs in body hairs, and position of accessory rhinaria. Ossiannilsson (1953),Quednau (2010)
Saltusaphis3 spp. Europe to E Siberia, Africa, now in N&S America
Feed on sedges (Carex, Cyperus, Scirpus. Monoecious holocyclic.
Apterae long-bodied, greyish yellow to greenish yellow, mottled with dark markings and
powdered with thin layer of greyish white wax. Front of head straight, or weakly produced medially. Tergites II-VI or III-VI more or less fused. Dorsum of body with variable amounts of sclerotization from mottled to almost completely dark. Dorsal body hairs short, fan-shaped or elongate, with pointed or slightly expanded apices. Posterior margin of tergite VIII with pair of processes each bearing 1-2 rod-shaped or pointed hairs. Siphunculi short, cylindrical, on border between tergites V & VI. Alate has broad dark dorsal abdominal cross bars & wings with dark spots on apices of veins. Related to Iziphya but siphunculi placed further back. Quednau (2010)
Copyright Marko Šćiban, all rights reserved
Only species, Sminthuraphis ulrichi, feeds on ground-level stems of sedges (Carex, Cyperaceae). Monoecious holocyclic.
Apterae medium-sized, plump-bodied, covered in bluish white wax. Antennae rather thin, segment III smooth without spicules, and accessory rhinaria of antennal segment VI adjacent to primary rhinarium, Margins of head sloping from antennal socket to anterior margin of eye. Body globular, 1.3-1.5 x longer than its greatest width. Dorsum of body with thin pointed hairs, surrounded by clusters of wax gland discs. Siphunculi poriform, situated between tergites V & VI. Alatae have similar wax glands to apterae. Wing veins bordered, with dark spots at ends. Quednau (2010)
Only species, Strenaphis elongata feeds on sedges (Carex, Cyperaceae). Monoecious holocyclic.
Apterae rather large, very long-bodied, yellow to orange-yellow, with paired dark orange flecks on dorsal abdomen. Front of head has dome-like protrusion that reaches level of apices of antennal segment I. Dorsum of body pale, or with few mutually free pale sclerites. Dorsal body hairs mostly short, fan-shaped, but on posterior abdomen rod-shaped. Siphunculi weakly elevated, almost poriform, on tergite VI. Related to Saltusaphis, but that has front of head more or less straight. Wings of alate without spots on apices of veins. Quednau (2010)
Only species, Subiziphya clauseni, most likely feeds on sedges (Carex, Cyperaceae), although first found on Poa.
Apterae medium-sized, long bodied, probably dark in life, with antennae black except at bases.
Frons with slight median bulge. Antennae shorter than body. Dorsum of body largely sclerotic, with membranous zones. Tergites II-VI fused. Abdomen often with 2 brown longitudinal bands extending to tergite VII. Dorsal body hairs numerous, exclusively mushroom-shaped. Tergite VIII rounded, without processes, and very hairy with about 50 hairs. Related to Iziphya and Saltusaphis, but distinguished by exclusively mushroom-shaped dorsal hairs and distinctive hairy tergite VIII. Alatae have broad dark dorsal abdominal cross-bars, bordered wing veins with spots at their apices. Quednau (2010)
Allaphis12 spp. N Hemisphere, + 1 (now?) in Australia & NZ
Feed on sedges (Carex, Cyperaceae).
Apterae medium sized, narrowly elliptical, usually yellow or greenish, with wax secretion. Antennal tubercles poorly developed, median frontal tubercle often prominent. Antennae 6-segmented; few secondary rhinaria on segment III in apterae; more on III-IV in alatae. Ocular tubercles absent. Femora not greatly enlarged. First tarsal segments with 5 hairs. Empodial hairs bristle-like. Hairs on abdomen and thorax mostly short and inconspicuous. Abdominal tergites III-VI are fused. Dorsum has conspicuous nodules. Abdominal dorsum on alate has separate sclerotic transverse bars on each tergite, which may be fused to form a dark sclerotic patch. Abdominal tergite VIII is rounded, weakly bifid, or with a distinct median protrusion on the posterior margin. Anal plate bilobed. Cauda knobbed. Other genera in the Saltusaphidini have fan-shaped empodial hairs. Quednau (2010)
Only species, Neosaltusaphis bodenheimeri, thought to feed on Carex, but swept from meadow with other Cyperaceae present.
Apterae medium-sized, straw-coloured, with antennae black on distal halves. Frons with median protrusion. Compound eye with weakly developed ocular tubercle. Tergites III-VI fused. Anterior corners of pronotum & posterior corners of abdominal tergite VIII developed into processes. Tergite VIII deeply incised until middle of tergite. Dorsal hairs minute and fan-shaped. Siphunculi somewhat raised above surface, rarely poriform. Alatae unknown. Related to Subsaltusaphis, but that genus without processes on tergite VIII, and dorsal hairs mushroom- or umbrella-shaped. Hille Ris Lambers (1961),Quednau (2010)
Peltaphis1 sp. Illinois, Wisconsin, USA, Quebec, Canada
Only species, Peltaphis hottesi feeds on the sedge Carex filiformis (Cyperaceae). Monoecious holocyclic.
Medium-sized, body oval & flattened, dark brown to almost black, with sclerotic carapace. Head broadly produced forward. Eyes prominent, without ocular tubercles. Secondary rhinaria absent. Abdominal tergites II-VI fused together. Long dorsal hairs often with furcate apices. Alatae are unknown. Frison & Ross (1933),Quednau (2010)
Subsaltusaphis13 spp. N hemisphere, mainly N Europe
Small to medium-sized, long-bodied, usually pale yellow aphids. Frons with median protrusion weakly developed. Compound eyes without ocular tubercles. Apterae lack secondary rhinaria. Empodial hairs are spatulate. Dorsal hairs are mostly very short and mushroom-shaped, with an incised cap so that they are stellate in dorsal view. No processes on tergite VIII. Alatae have dark central abdominal patch on tergites III-V, incised between segments. All feed on sedges (Carex, Cyperaceae).
Apterae medium sized, slender, usually brown, orange or green. Antennae often stout; apterae often have rhinaria on antennal segment III, alatae on segments IV & V. Tergites usually mutually free, also meso- and metanotum mostly separated. Ventral abdominal sclerites often developed. Empodial hairs spatulate. Dorsal body hairs mostly pointed, rarely mushroom- or star-shaped. On dorsum wax gland pores sometimes present around hairs in form of scattered pits, more rarely of cribriform discs. Tergite VIII rounded or shallowly indented., Siphunculi nearly poriform, hardly raised above surface. Alatae usually have extensive dark dorsal cross bands, sometimes merging into a solid patch. Related to Subsaltusaphis but with dorsal hairs mostly pointed. Quednau (2010)
Copyright Marko Šćiban, all rights reserved.
Shivaphis8 spp. Turkey to Japan, invasive in USA, Australia, South Africa
All species monoecious holocyclic on hackberry (Celtis) or blue sandalwood (Pterocallis).
Apterae mostly medium sized, green, yellow or red-brown. Head grooved in front, without antennal tubercles. Antennae long, ringed with black; segment VI has nail-like process as in Lachninae. Rostrum elongate, but only reaches between fore & middle coxae. Secondary rhinaria somewhat elliptical. Wings of alate have cubitus twice forked, with fuscous-bordered veins ending in pigmented triangles. Abdomen ovate, with four rows of wax glands; these also present on head & thorax & secrete flocculent wax. Siphunculi ring-like, small, almost flush with dorsum. Cauda well developed, cylindrical, resting upon a broad base. Anal plate deeply bilobed. Das (1918),Quednau (2003)
Appendiseta1 sp. Orig. N. America, now also Chile, Argentina, Europe, Middle East
Only species, Appendiseta robiniae, monoecious holocyclic especially on black locust (Robinia pseudacacia), also Robinia neomexicana & Sophora japonica (all Fabaceae).
All viviparae alate. Alatae medium-sized, yellow-green with rows of wax spots. Frontal tubercles poorly developed. Frontal ocellus at least partially hidden when head is viewed from above. Antenna 6-segmented, with narrowly oval secondary rhinaria. Legs mostly with pointed hairs. Pronotum with two anterior and two posterior spinal hairs. First tarsal segments with two dorsal hairs, seven ventral. Abdominal segments I and II with weak spinal tubercles that are single or weakly divided. Dorsal abdominal hairs minute, weakly capitate. Siphunculi short & smooth, with hair near its base on the ventral surface. Cauda knobbed. Anal plate deeply indented. Related to Pterocallis, differ in chaetotaxy. Richards (1965)
Feed on milk vetch (Astralagus, Fabaceae). Monoecious holocyclic.
Apterae rather small to medium sized, brownish or yellow; alatae of some species unknown. Ventral face of head devoid of pigmented transverse band. Forehead with a variably developed median projection. Accessory rhinaria on antennal segment VI in two separate groups. Segment III smooth except for apex; bears conspicuous hairs, often longer than basal diameter of segment. Terminal process shorter than base of antennal segment VI. Anterior coxae greatly enlarged. Empodial hairs rod shaped. Knob of cauda with conical dorsal process. Related to Therioaphis, but process on cauda and host distinctive. Remaudiere (1989)
Feed on elm (Ulmus), mainly Siberian elm (Ulmus pumila) and Japanese elm (Ulmus davidiana var japonica). Probably monoecious holocyclic.
All adult viviparae alate. Plump-bodied rather large, green aphids, with wing veins dark-bordered. Antennal tubercles absent. Dorsal wax pores between antennae. Antennae much shorter than body, with secondary rhinaria on segment III; terminal process shorter than the base of antennal segment VI. Wings distinctly dark along the veins; pterostigma truncated. Body without pigmented sclerites; has spinal tubercles and spinules, with many moderate or long pointed hairs. Legs have many long hairs, & fore-coxae not enlarged. Siphunculi short, truncated and smooth. Cauda constricted at base and globular. Anal plate distinctly bilobed. Related to Calaphis, but differs in presence of wax pores on head, lack of pigmented sclerites on the body, and shorter globular cauda. Differs from Chromaphis in wax pores on head, and deeply bilobed anal plate. Takahashi (1961)
Feeds on shoots and undersides of leaves of bamboos (Bambusa, Dendrocalamus, Pseudosasa, Indocalamus, Poaceae). Very active, jumping when disturbed. Sexuales not reported, one species thought to be anholocyclic in Taiwan.
All adult viviparae alate. Medium-sized, dark green or dark purple to black. Frontal tubercles not well developed. Post clypeus without a projection. Antennae 6-segmented, with circular secondary rhinaria; terminal process more or less equal to base antennal segment VI. Wing venation normal, veins clear without infuscation. Head and thorax without tubercles. Abdomen with very large tubercles, larger than siphunculi. Siphunculi truncate, little longer than wide. Cauda knobbed. Anal plate cleft. Closely related to Tuberculatus subgenus Nippocallis, but differs re lack of tubercles on both head and thorax. Tao (1963),Quednau (2003)
Feeds on bamboos (Yushania, Arundinaria). Life cycle unknown.
All adult viviparae alate. Alatae of Cranaphis formosana long-bodied, yellow with black antennae, broad medial stripe on head and prothorax, paired dusky-dark markings on most abdominal tergites. Head with epicranial suture, Rostrum reaching a little beyond fore coxae, with apical rostral segment about as long as its greatest basal width. Spinal hairs of tergite VII much displaced laterally. Marginal sclerites on tergites II-IV(V) with processes developed as small cones. Siphunculi very short, almost poriform. Closely related to Tinocalloides, but specialised for bamboo. Quednau (2003)
Indiochaitophorus1 sp. Kashmir, Himachal Pradesh, India, Pakistan
Only species, Indiochaitophorus furcatus, feeds on undersides of leaves and twigs of Himalayan elm (Ulmus wallichiana), cherry-bark elm (Ulmus villosa) (both Ulmaceae). Life cycle unknown.
Apterae medium sized, elongate oval, pale brown with thick black dorsal longitudinal stripes. Antennae 6-segmented, with hairs on segment about equal in length to basal diameter of segment; terminal process very short. Secondary rhinaria absent in aptera, strongly transverse in alatae. Rostrum with thickened heart-shaped basal ridge. Wing venation normal with unbordered forewings. Legs normal, but fore coxae in alatae enlarged. Abdomen with well developed large dark spino-pleural and marginal sclerites, each bearing two very stout primary hairs, and numerous shorter hairs. Siphunculi small, truncate with basal hair. Cauda knobbed. Related to Chromocallis, but with shorter antennal hairs, unbordered forewing veins and sclerites on aptera. Verma (1969),Quednau (2003)
Only species, Melanocallis caryaefoliae, feeds on both upper and lower sides of leaves of hickory (Carya, Juglandaceae), especially Carya illinoisensis. Feeding causes yellow spots on leaves. Monoecious holocyclic.
All viviparae alate. Alatae rather small, squat-bodied, olive green to reddish brown to blackish with large paired black dorsal tubercles, especially large on tergite II. Abdomen has series of conspicuous, white wax spots. Wings held upright at rest. The pronotum has wart-like spinal processes, the mesonotum has large cone-like processes, and the metanotum has short processes. Abdominal tergite II has a bifid process, and other tergites have dark, sclerotic, short finger-like processes. Siphunculi truncate, cauda knobbed. Close to Tinocallis, but distinguished by body shape, abdominal marginal sclerites, and host. Quednau (2003)
Only species, Quednaucallis nigropunctata, feeds on hardy rosewood (Dalbergia hupeana, Fabaceae). Life cycle unknown.
Alatae of Quednaucallis nigropunctata are medium-sized, yellowish-white with banded antennae and dark spot on wing at base of pterostigma. Pro-, meso- & metathoracic tergites without distinct spinal tubercles. Spinal tubercles on abdomen of nearly same height on all tergites. Spinal hairs of tergites I-VI arranged as two parallel longitudinal rows, only those of tergite VII displaced laterally. Closely related to Tinocallis, but without lateral displacement of spinal hairs on tergites III & V. Chakrabarti (1988)
Sarucallis1 sp. orig across E. & S.E. Asia; now also Europe, Iran, USA, C. America, Caribbean, S. America, Australia
Only species, Sarucallis kahawaluokalani, Feeds on undersides of leaves of crape myrtle (Lagerstroemia indica) and henna (Lawsonia alba) (both Lythraceae). Monoecious holocyclic in temperate areas.
All viviparae alate. Alatae medium-sized, yellowish with dark brown markings, & white wax tufts on head and thorax. Vertex marked with 2 black marginal stripes & narrow black stripe medially. Secondary rhinaria on antennae narrow elliptical; terminal process slightly longer than base of antennal segment VI. Forecoxae greatly enlarged. Wings held flat over body in repose. Extensive black pigment over costal field and below, extending to base of wing; pterostigma is almost black with a crescent-shaped spot below. Tergite I has a pair of short cone-shaped black spinal processes. Tergite II has large bifid process on dark spinopleural bar. Marginal sclerites of tergites II-IV developed as short cone-shaped processes. Siphunculi black or partially sclerotic, cylindrical. Quednau (2003)
Two species feeding on bamboo (Bambusa, Poaceae). Probably monoecious holocyclic.
All viviparae alate. Alatae medium-sized, probably wax covered. Clypeus with nose-like anterior projection. Epicranial suture present. Antennae 6-segmented, with terminal process very short, only 0.24-0.55 x base of segment VI. First tarsal segments with 5 ventral & 2 dorsal hairs. Tibiae with thick spine-like hairs at apex. Also minute wax pores on tibiae, as well as on antennae, tips of femora and spinal hair-bearing areas of abdomen. Abdominal dorsum with variably developed sclerotic patches spinally on segments I-V & VIII. Siphunculi cylindrical, lacking wax pores. Cauda with globular apex, anal plate not very deeply cleft. Resemble Takecallis in anterior projection of clypeus, but differ in terminal process to base ratio. Raychaudhuri & Pal (1974)
Takecallis8 spp. China to Japan, some now in Europe, a few N America, Australia
Feed on bamboo (Arundinaria, Bambusa, Phyllostachys, Sasa, Poaceae). Populations often anholocyclic, but sexuales present in East Asia.
Usually all viviparae alate. Small delicate narrow-bodied, greyish-yellow or pale green, often with wax powder. Clypeus bears forward-directed tubercle. Antennae 6-segmented with secondary rhinaria on segment III; terminal process more or less equal to length of base of segment VI. Frontal tubercles very low. Rostrum extremely short. Front coxae enlarged, used for jumping. Spinal hairs on small humps, marginal hairs of tergites II-IV on more or less well-developed marginal tubercles. Spinal hairs of tergite VI closer together, those of tergite VII further apart, than those of tergites I-V. Cauda knobbed, anal plate bilobed. Immatures have long capitate hairs. Stroyan (1977)
Therioaphis25 spp. Europe to Japan, 2 now in N&S America, 1 also in S. Africa, Australia
Therioaphis feed on members of the pea and bean family (Fabaceae). Monoecious holocyclic.
Viviparae may be apterous or alate (all alate for one species). Rather small to medium-sized yellowish aphids, spotted with dark grey hair-bearing scleroites. Wings with veins dark bordered. Head has ventral dark band running transversely between inner margins of compound eyes. Terminal process about same length as base antennal segment VI; antennal hairs shorter than basal diameter of segment III. Rostrum short, not reaching middle coxae. Front coxae very much enlarged. Siphunculi stump-shaped, flangeless, and variably rugose, close to marginal sclerite of tergite VI. Cauda rather large, with elongate knob. Stroyan (1977)
Tinocallis20 spp. Europe to Japan, 1 in N America, 2 now there
Most species feed on elms (Ulmaceae), some on Lythraceae and other families. Monoecious holocyclic. Not attended by ants.
All viviparae alate. Rather small to medium-sized, whitish to yellowish green, some with conspicuous black markings. Often with wax spots. Antennae as long as or shorter than the body, with terminal process shorter than base; secondary rhinaria on segment III. Antennal hairs short. Head with small frontal tubercles, and often paired hair-bearing processes. Large hair-bearing subconical processes sometimes present on pronotum & mesonotum. Abdomen typically with one pair of spinal and one pair of marginal hairs per tergite on segments I-VII, sometimes set on tubercles; tergite VIII with a single median pair of spinals. Spinal hairs of tergites III, V and VII laterally displaced. Siphunculi stump-shaped, situated on tergite VI. Cauda knobbed, with about 8-18 hairs. Immatures with capitate dorsal hairs. Stroyan (1977)
Only species, Tinocalloides montanus, feeds on undersides of leaves of cherry (Prunus cerasus, Prunus cerasoides, Prunus napaulensis) & peach (Prunus persica). Monoecious holocyclic.
All viviparae alate. Medium-sized, pale yellow abdomen with two widely-separated rows of black spino-pleural patches. Without antennal tubercles. Antennae 6-segmented with secondary rhinaria on segment III. Dorsal tubercles confined to marginal sclerites on presiphuncular sclerites. Spinal processes absent. Dorsal hairs fine & short, regularly arranged. Spinal hairs in straight lines. Siphunculi truncate, with hair. Cauda knobbed. Anal plate bilobed. Basu (1970)
Only species, Chaitogenophorus yuzhongensis, feeds on Korean aspen (Populus davidiana, Salicaceae).
Rather small, elongate oval, dorsum black, yellow-green on ventral side. Head is separate from prothorax, abdominal segments VI & VII are free, and abdominal segments I-VI appear fused. Antennae 6-segmented, 0.73 x body length, with terminal process 2.70 x base of antennal segment VI. Apical rostral segment is thick and short, 0.57 x second hind tarsal segment. There are 5,5,5, hairs on the first tarsal segments. Body strongly sclerotized, with cuticle covered with dense short spines. Siphunculi truncate. Cauda constricted in middle, with 6-7 hairs at end. Genital plate is wedge shaped. Zhang et al. (1999)
Chaitophorus93 spp. N hemisphere, 1 now in S America, S Africa
Feed on either poplar (Populus) or willow (Salix) in the Salicaceae. Monoecious holocyclic. May be ant attended.
Very hairy, rather small to medium-sized aphids, oval, more or less elongate, and variably flattened, ranging from whitish, yellow, green, brownish to black; never with flocculent wax or wax powder. Dorsal cuticle of apterae is largely sclerotized. Tergites II-VI often fused. Siphunculi short and stump-shaped. Cauda usually knobbed with a rather small number of hairs. Winged forms often have dark segmental cross-bands & marginal sclerites. Stroyan (1977)
Only species, Glyphochaitophorus cristaphis, feeds on Japanese maple (Acer palmatum, Aceraceae)
Body has conspicuous median dorsal ridge. Head fused with prothorax, meso- and metathorax fused, abdominal segments I-VII fused & segment VIII free. Antennae 5-segmented in apterae, 6-segmented
in alatae; segment III with 9-10 round secondary rhinaria in alatae. Rostrum short, ultimate rostral segment thick and wedge-shaped, First tarsal segments with 5 hairs. Dorsal cuticle with very well-developed "O"- and "C"-shaped or irregularly shaped wart-like sculpturing. Hairs on head and dorsal hairs on abdominal tergite VIII long thick & blunt, arising from distinct tubercles. Siphunculi short, truncated. Cauda knobbed. Anal plate entire, broadly rounded, genital plate transverse oval. Chen et al (2021)
Lambersaphis1 sp. Kazakhstan, Tadzhikistan, Iran, China
Only species, Lambersaphis pruinosae, feeds on Euphrates poplar (Populus eupratica (= P. diversifolia) & Populus pruinosa (both in Salicaceae).
Apterae medium-sized, oval, blackish brown. Head, prothorax, mesothorax, metathorax & segment VIII are free, segments I-VII are fused with each other. Antennal tubercles slightly developed, median frontal tubercle undeveloped. Antennae about 0.62 x body, with terminal process very short at 0.67-0.75 x base of antennal segment VI. Dorsal hairs are sparse, short 7 needle-like. Siphunculi crater-like, without reticulate sculpturing. Cauda semicircular, with 20-22 hairs. Alatae have thickly fuscous-bordered wing veins like the North American Chaitophorus populicola.Qiao et al. (2003)
Periphyllus50 spp. Most in Europe to Japan, 3 N America + 3 now in N America, Australasia
Most live on maples and sycamore (Acer, Aceraceae). Monoecious holocyclic. Some species usually ant-attended. Show seasonal polymorphism. Several species have aestivating nymphal stage which is often flattened and hairy.
Medium-sized to large elongate oval or pear-shaped aphids which may be winged or wingless. Dorsum mainly membranous (unsclerotized), but many small hair-bearing plates. The siphunculi are stump-shaped with a pronounced flange. Cauda at tip of the abdomen is either rounded or tongue-shaped with a slight constriction. Antennal hairs usually long and conspicuous. Stroyan (1977)
Only 2 species in genus, both feeding on stem base or roots of quaking aspen (Populus tremuloides, Salicaceae). Monoecious holocyclic.
Apterae rather large, P. canadensis is grey or black, P. hughi is cream-coloured. Frontal tubercles undeveloped. Antennae 6-segmented, with distinctive long thick terminal process clothed with hairs like rest of antenna. Antennal segments III & IV often have secondary rhinaria. Rostrum rather long, extending to hind coxae. First tarsal segments each with 7 or 8 hairs. Abdominal hairs sparse & minute on tergum, long & conspicuous laterally. Siphunculi poriform or nearly so, sited on abdominal segment VI. Cauda rounded. Anal plate entire. Differ from Chaitophorus in hairy terminal process and poriform siphunculi. Richards (1972)
Most species feed on members of willow family (Aceraceae), one species on kiwifruit (Actinidia, Actinideaceae)
Apterae medium sized, green, yellow or brown, one glassy white. Head fused with pronotum. Antennal tubercles distinct, median frontal tubercles absent. Antennae 5-6 segmented, shorter than body, terminal process longer than base segment VI; antennae without secondary rhinaria in apterae.
Apical rostral segment shorter than second hind tarsal segment. First tarsal segments with 3-5 ventral hairs. Tergites I-VII or II-VII completely fused. Dorsum membranous, rugose or corrugated over entire surface. Long thick, hollow hairs around margin of body. Siphunculi short, truncate, without any reticulation. Cauda wider than long with 8-16 hairs. Distinguished from Chaitophorus & Periphyllus by fused head and pronotum, and lack of reticulation on siphunculi. Qiao et al. (2004)
Both species in genus feed on willow (Acer, Aceraceae). Biology unknown.
Apterae rather small, elongate oval, whitish or yellowish. Head fused with pronotum. Antennae 5-segmented, shorter than body. Secondary rhinaria absent on aptera. Apical rostral segment with 0-2 accessory hairs. First tarsal segment bearing 3 ventral hairs, without dorsal hairs. Abdominal segments I-VII solidly fused. Dorsal body covered with O- or C-like tubercles, and dorsal hairs of body long, thick, flattened with knobbed or blunt apices. Each segment bears paired marginal and spinal hairs on each side. Siphunculi short, truncate, not reticulated. Cauda rounded and anal plate broadly rounded. Related to Trichaitophorus, but with long, thick spinal as well as marginal hairs. Jiang et al. (2016)
Atheroides7 spp. Mainly Europe, also W to C Asia, 1 N America
Feed on grasses (Poaceae) and some sedges (Cyperaceae). Some species found on many species of grasses. Others are more specific such as Atheroides doncasteri on Deschampsia caespitosa.
Apterous viviparae of Atheroides have very elongate slender body. Head and prothorax not fused. Head+thorax+abdominal segment I almost as long as abdominal segments II-VIII. Antennae short, 5-segmented or for Atheroides brevicornis, 4-segmented. Frons convex. Rostrum short, reaching to middle coxae. Abdominal I-VII sclerotized and usually fused. Tergite VIII semicircular, covering the cauda. Siphunculi pore-like, placed at anterior margin of abdominal segment V. Cauda & anal plate broadly rounded. Wieczorek (2009)
Only species, Caricosipha paniculatae, feeds on greater tussock sedge (Carex paniculata) and true fox sedge (Carex vulpina), both in Cyperaceae.
Flattened pear-shaped aphids, broadest about the level of tergite IV. Dorsum & most of the venter blackish sclerotic, with abdominal tergites I-VII fused into a solid carapace. Head capsule fused with pronotum; mesonotum, metanotum and abdominal tergite VIII free. Antennae mainly pale & antennal tubercles very low. Antennal hairs nearly all long. Compound eyes very prominent, sited on lateral extensions of head. Rostrum does not reach middle coxae, with apical segment blunt. Siphunculi pale, smooth, truncate conical or stump-shaped, with marked flange. Cauda slightly knobbed with 5-8 hairs. Alatae have dorsal carapace broken into segmental dark bars & marginal sclerites. Secondary rhinaria only on antennal segment III. Stroyan (1977)
Chaetosiphella aphids feed on grasses (Poaceae). Sometimes attended by ants.
Apterae elongate bodied, grey-green or blackish. Antennae 5-segmented. Apical rostral segment usually very long and pointed. Hind legs long. Empodial hairs pointed or spatulate. Wings narrow with normal venation. Abdominal tergites II-VII fused & sclerotized. Dorsal hairs are pointed, thorn-like, placed on wart-like bases or with forked, jagged or fan-shaped apices. Siphunculi pore-shaped or slightly elevated, on the anterior part of the margin of abdominal segment V. Tergite VIII is normal, as in Sipha, not covering the cauda. Cauda & anal plate broadly rounded.
Only species, Laingia psammae feeds on many grasses (Poaceae), especially marram grass (Ammophila arenaria).
Apterae elongate, parallel-sided, mottled grey-green or straw-coloured. Antennae very short, 5-segmented with terminal process about 1.2-2.1 x as long base segment V. Antennal hairs rather sparse and thorn-like. All body tergites mutually free and membranous, largely occupied by variably pale or dusky sclerotic bands and marginal sclerites, these adorned with small blunt spinules in wavy rows that tend to form reticulations laterally. Primary spinal, pleural and marginal body hairs rather thorn-like, sometimes with split or ragged apices; smaller secondary hairs on each tergite. Siphunculi slightly elevated pores on abdominal tergite VI, as opposed to tergite V in Atheroides. Also that genus has dorsal carapace sclerotized. Stroyan (1977)
Sipha11 spp. N hemisphere, 2 now in S America, Africa
Sipha feed on grasses (Poaceae). Several species restricted to wetland or coastal habitats.
Medium-sized oval aphids with conspicuous spiny hairs. Antennae 5-segmented, up to about 0.4 x body length. Rostrum short, reaching about to middle coxae
First tarsal segments with 3-5 hairs. Dorsum usually rather solidly sclerotic, with membranous intersegments between head, thoracic tergites, abdominal tergites I/II and VII/VIII. Sclerotic dorsal cuticle either smooth or rather thickly adorned with fine to strong denticles or nodules, Dorsal body hairs rather stout, typically in a more or less staggered double row across abdominal tergites. Siphunculi truncate conical, with a distinct flange, located on abdominal tergite 5 level with spiracles. Cauda broadly rounded (subgenus Rungsia) or with small constriction demarcating apical knob (subgenus Sipha). Stroyan (1977)
All feeding on maples (Aceraceae). Monoecious holocyclic. Native to North America, but Drepanaphis acerifoliae invasive in continental Europe.
All adult viviparae winged. Antennal tubercles developed. Antenna 6-segmented, with elongate terminal process; secondary rhinaria on antennal segment III only. Rostrum 4-segmented. Prothorax & abdomen without marginal tubercles. Fore femur flared apically. First tarsal segments with 5-6 ventral &2 dorsal hairs. Abdominal hairs arranged in single irregular transverse row on each tergite; on tergites I-IV commonly on tubercles that are variably developed and often conspicuously pigmented. Pigmented marginal sclerites commonly present. Siphunculi flask-shaped, wider at base than apex, without hairs, with apical flange, not fused with marginal sclerite of abdominal segment. Abdominal tergite VIII entire. Cauda knobbed. Anal plate somewhat bilobed. Footit & Richards (1993)
Drepanosiphoniella3 spp. High in S Europe, SW Asia, Morocco
Main host is Montellier maple (Acer monspessulanum), also Persian maple (Acer velutinum). All three species generally found at altitudes more than 1000 m.a.sl. Monoecious holocyclic.
Both apterous and alate viviparae occur as in Chaitophorinae. Medium sized to rather large, grey to brown. Antennae 6-segmented. All morphs with rounded secondary rhinaria on antennal segment III. Primary & secondary rhinaria with sclerotic ring, without fringe of hairs. Rostrum reaching to hind coxae. First tarsal chaetotaxy 7,7,7. Distal parts of tibiae with small spinules. Hind tibiae with small rastral spines. Abdominal tergites with rather small spinal, pleural and marginal tubercles and long, stiff hairs arising from each tubercle. Siphunculi with well-developed flange. Anal plate bilobed. Related to the nearctic genus Drepanaphis, but primary rhinaria have no fringe of hairs & dorsal body hairs are long & stiff. Wieczorek,et al (2015)
Drepanosiphum10 spp. Europe, W Asia, Mediterranean, 1 N America, 1 now almost WW
All live on leaves of sycamore or maple (Aceraceae). Form spaced-out aggregations on undersides of leaves in shade. Monoecious holocyclic. Not attended by ants.
All viviparae winged. Medium-sized to large, elongate long-legged aphids; yellowish, brown or green. Antennae 6-segmented, with secondary rhinaria on basal part of antennal segment III; Accessory rhinaria on antennal segment VI partly separated from the primary rhinarium. Antennal hairs fine and acute. Rostrum short, not
reaching middle pair of coxae. First tarsal segments typically with 7 ventral and 2 dorsal hairs. Wing veins not shadowed, but sometimes with a small apical triangular spot. Siphunculi situated level with spinal hairs of tergite 5; long, vasiform, with a strong and deep constriction immediately before the sharp apical flange. Cauda small, with a basal subtriangular part followed by a slight constriction delimiting a knob bearing typically 5 hairs. Stroyan (1977)
Only species, Shenahweum minutum, feeds on sugar maple (Acer saccharum, Aceraceae). Monoecious holocyclic.
All viviparae alate. Alatae are rather small, with brown or black thorax & pale greenish-yellow to whitish abdomen. Antennae 6-segmented. Fore wings with media twice forked.
Dorsum of abdomen without tubercles. Siphunculi small, cylindrical, tapering to tip, without flange. Cauda rounded at apex, showing almost no constriction. Anal plate scarcely indented. Differs from Drepanaphis in having differently shaped siphunculi, anal plate less indented, cauda not knobbed, & lack of prominent dorsal tubercles. Hottes & Frison (1931)
All species feed on maple (Acer, Aceraceae). Where known, monoecious holocyclic.
All viviparae alate. Frontal tubercles conspicuous. Antennae long, nearly 1.5 x body, with terminal process up to 3 x base segment VI. Secondary rhinaria elongated & with hairy fringe. Rostrum short. Fore femora enlarged. First tarsal segment with pair of dorsal hairs. Empodial hairs spatulate. Abdomen without dorsal processes. Marginal sclerite with 1 long and some shorter hairs. Tergite VIII with 4 hairs. Siphunculi long, enlarged at base, curved near apices and reticulated at apex. Cauda broadly conical, short. Differ from Nearctic Drepanaphis by lack of dorsal processes, often having dark pigment on forewings, & distal reticulation on the siphunculi. Matsumura (1917),Higuchi (1972)
Aphidounguis1-2 spp. China to Japan, now in N Carolina, USA
Aphidounguis mali , host-alternates between Chinese elm (Ulmus parvifolia, Ulmaceae), where it creates cluster galls consisting of several rolled leaves, and roots of apple (Malus, Rosaceae). The other species is disputed.
Apterae on secondary host are small white oval aphids secreting wax wool. Antennae short, 4-5 segmented, with very short terminal process; secondary rhinaria are absent. Antennae & abdomen have long fine hairs. Abdomen has well developed wax plates, 4 on each of tergites I-VII, 2 on tergite VIII. Many elongate parts are arranged in a compact circle, with each plate comprising 1-4 such circles fused together. Legs are distinctive feature in that one of the claws on each leg is much reduced or entirely wanting. Siphunculi absent. Cauda very short and rounded. There is some evidence that Schizoneurella is closely related to Aphidounguis.Takahashi (1963),Akimoto (1983)
Byrsocryptoides zelkovae host alternates between Zelkova (Ulmaceae), where they live in rolled leaf pseudogalls, and aerial parts of Carex (Cyperaceae); Byrsocryptoides zelkovaecola known only from Zelkova
Fundatrix in gall is oval, yellowish-green, covered in wax. Body covered with sparse bristle-like hairs. Eyes are triommatidia. Antennae 4-segmented, very short about 0.17 x body. Alate spring migrants, emerging from pseudogalls on Zelkova, are small, rather long-bodied, with dark brown head, meso- and metathorax and pale yellow to green prothorax and abdomen. Antennae are 6-segmented. They have an unbranched media, only one oblique vein in the hind wing, and inconspicuous ring-like siphunculi. Resemble Kaltenbachiella, but in Byrsocryptoides secondary rhinaria terminal process is relatively longer. Genus thought to be in basal position in the tribe Eriosomatini. Dzhibladze (1960)
Three species host alternate between elm (Ulmus, Ulmaceae), where they live in cockscomb-like galls on leaf lamina, to grasses (Poaceae) or sedges (Cyperaceae), where they live on the roots or aerial parts. Three species live parthenogenetically year-round on grasses and sedges.
Related to genus Kaltenbachiella. Apterae on the secondary host differ from Kaltenbachiella apterae in having the fore-tarsi parallel-sided, with a ventral hair arising from a distal protrusion. Alatae differ in having a once-branched media in the fore wing and one oblique vein in the hind wing. Blackman & Eastop (1982-)
Colophina5 spp. China to Japan, 1 now in New Zealand
Three of species host alternate between Zelkova (Ulmaceae), where form globular galls, and Clematis (Ranunculaceae), where live on aerial parts. Other species only found on Clematis. Have unusually complex life cycles and polymorphism, including sterile first instar soldiers on secondary host.
Similar to Eriosoma aphids, but wax glands of the apterae form 6 longitudinal rows, and have small facets like those in the tribe Pemphigini. Blackman & Eastop (1982-)
Most species host alternate between galls on elm (Ulmus, Ulmaceae) and secondary hosts such as apple (Malus, Rosaceae) and currants (Ribes, Grossulariaceae). Holocyclic. Not attended by ants.
Rather small to medium-sized, usually dark coloured; most stages (including winged forms) are covered in dense flocculent wax. Both winged and wingless aphids have rather conspicuous siphuncular pores with partially chitinized rims surrounded by ring of hairs. Forewing of winged individuals usually has only one branch in medial vein. Blackman & Eastop (1982-)
Gharesia1 sp. Pakistan, California, USA, British Columbia, Canada
Feeds on sedges (Carex, Kobresia, Cyperaceae). Some populations anholocyclic, but may host alternate where endemic.
Medium-sized, rather elongate aphids, appearing greyish due to flocculent wax covering. Apterae have 5-segmented antennae, with more or less conical terminal process. Primary rhinaria small, thick-rimmed with 3-4 small accessory rhinaria. Compound eyes represented only by triommatidia. Head, thorax and abdomen each with an array of wax gland plates, each plate composed of rather even-sized facets. Legs short and very sparsely haired. Siphuncular pores absent. Abdominal spiracles small and slit-like. First tarsal segments with 3,2,2 hairs; second tarsal segments with empodial hairs. Anal plate somewhat angularly produced, extending back beyond cauda, so that anus is dorsal. Possibly related to Byrsocryptoides, but with much shorter rostrum. Stroyan (1983)
Hemipodaphis monstroa was described from monocot host in India (possible secondary host). Hemipodaphis persimilis was described from leaf-roll galls on Zelkova serrata (see here) in Japan. Unclear whether two species in same genus.
Apterae on secondary host have hemispherical nodules all over dorsum. Antennae 3-segmented. Eyes triommatidia. Rostrum short, but stylets very long, about 3 x rostrum. Circular pit-like wax plates on head, thorax & abdomen; plates have thick rim with 3-6 granular facets. Hairs on head, thorax, and abdomen sparse, long and thick. Posterior margin of body with thick black covering. Siphunculi absent. Defining features of genus are long stylet and the nodular dorsum. Emigrant alate from galls have very short & dark, 6-segmented antennae. Second tarsal
segment intensively spinose; empodial hairs slightly longer than claws. Fore wings with media once branched
and hind wings with 2 cubital veins. Abdomen without pigmented intersegmental bands, not
sclerotized except for anal and genital plates. Abdominal hairs scanty and short. Siphunculi present on abdominal tergite V only showing a very small rimmed opening. David & Rajasingh (1972),Akimoto (1983)
Kaltenbachiella8 spp. India to Japan, N America, 1 in Europe & N Africa
Most Kaltenbachiella use elm (Ulmus, Ulmaceae) as their primary host, secondary hosts mainly Lamiaceae. Related to Colopha and Tetraneura, but instead of producing gall on leaf lamina, Kaltenbachiella fundatrices induce gall near base of leaf mid-rib.
Emigrant alate is medium-sized, mostly grey-green or blue-greyish without wax plates. Antennae about 0.4 x body. Primary rhinaria not surrounded by short hairs. Hind wing of Kaltenbachiella has two oblique veins. All tarsi 2-segmented. Siphuncular pores absent. Heie (1980)
Paracolopha2 spp. Japan & S China, now in Europe & N America
Paracolopha morrisoni host alternates from Japanese zelkova (Zelkova serrata, Ulmaceae) to roots of small bamboos (Sasa, Poaceae), or may persist parthenogenetically on bamboo roots. Paracolopha takahashii only known from secondary host, sedge Carex breviculmis (Cyperaceae).
Emigrant alate has body elongate oval, without wax gland plates. Antennae very short, 6-segmented. Fore wings with unbranched media; the veins rather broad, not conspicuously bordered. Hind wings with only 1 oblique vein. Alate is without siphunculi. Aptera on secondary host is globular, pale yellow, covered with white filamentous wax. Antennae very short, 5-6-segmented. Legs short. First segment of the fore-tarsi thickened and projects anteriorly. Rostrum is long. Wax gland plates arranged longitudinally in 6 rows, reduced to 4 rows in abdominal tergites V-VII, 2 rows in tergite VIII. Siphunculi on tergite V displaced towards midline, surrounded thinly by hairs. Akimoto (1985),Blackman et al. (2019)
Only species is Schizoneurata tissoti. Only known morphs are sexuparae and IV instar alatoid nymphs found feeding on one-flowered hawthorn (Crataegus uniflora, Rosaceae). Primary host presumed to be elm (Ulmaceae).
Apterae and immatures presumably wax-covered. Sexuparae and alatoid nymphs without siphunculi. Alatoid nymphs have spinal & marginal wax glands; wax glands resemble those in Colopha and Schizoneurella. Tarsi 2-segmented, middle hair on underside of first segment of fore tarsi not on short process. Empodial hairs in larvae longer than claws. Hille Ris Lambers (1973)
Schizoneurella1 sp. Jammu, Kashmir, India, Pakistan, ?China
Only species, Schizoneurella indica, induces open leaf-roll pseudogalls on its primary host, Marn elm (Ulmus villosa, Ulmaceae). It migrates to its secondary host apple (Malus pumila (= Malus domestica, Rosaceae), where colonies live, most likely covered in woolly wax, on the roots.
Empodial hairs absent in apterae on secondary host, reduced in alatae. without siphunculi in the morphs on the secondary host. Distinct from the nearctic genus Schizoneurata because it has embryos with spinulose hind tarsi, as in palaearctic Eriosoma. The species may be close to Aphidounguis.Hille Ris Lambers (1973)
Siciunguis decima feeds on apple (Malus); Siciunguis novena feeds on
pear (Pyrus), both in Rosaceae.
Apterae secrete white wax powder. Antennae 6-segmented, primary rhinaria small, round, ciliated; secondary rhinaria linear elongate. First tarsal segments have 3,3,3 hairs. Tarsi 2-segmented. Four longitudinal rows of wax gland plates on dorsum of body. Siphunculi sited on tergite V in apterae, on tergite VI in alatae; protuberant surrounded by few fine, sharp-pointed hairs. Cauda and anal plate rounded. Alate has media of forewing once forked; hind wing with 2 oblique veins. Blackman in AWP comments that Siciunguis Zhang & Qiao should probably be treated as a synonym of Eriosoma.Zhang et al (1999)
Tetraneura37 spp. Palaearctic, 3 now in N America, 1 near WW
Some species host alternate between galls on leaf lamina of elm (Ulmaceae) and roots of grasses (Poaceae). Galls are red, yellow or green, stalked, pouch-like. Holocyclic, but many species only known from grass roots as anholocyclic populations. Not attended by ants.
Medium-sized aphids. Wax gland plates may be present or absent. Antennae 3- or 4-segmented in fundatrices, 5- or 6-segmented in apterous females on secondary hosts; usually 6-segmented in alate females. Apterae have one-segmented tarsi. Alatae have simple, unbranched media vein in forewing. Siphuncular pores present or absent.
Heie (1980)
Both species gall Zelkova (Ulmaceae). Zelkovaphis caucasica forms leaf-roll galls, Z. trinacriae forms rosette-like nest of thickened leaves. Dioecious holocyclic. Emigrant alatae of 1 species fly to Carex. For pictures of galls see here.
Fundatrices, grey or green, covered in white wax. Emigrant alatae medium-sized, blackish. Antennae rather short, 6-segmented with ring like rhinaria on segments III-V. Rostrum reaching second pair of coxae. Abdomen largely membranous. Wax gland plates not differentiated. First tarsal segments have 3,2,2, or 3,3,3 hairs. Media one-forked, hind wings with 2 cubital veins. Siphunculi behind tergite V, pore-like or slightly elevated & cone-shaped, surrounded by few hairs. Cauda narrow sclerotized arch with 2 hairs. Barbagallo (2002)
Aloephagus1 sp. orig? across Africa, USA, Europe, Japan, Australia
Only species, Aloephagus myersi, presumed to have a sexual phase in Africa on primary host Pistacia aethiopica (Anacardiaceae). Mainly known on secondary host, Aloe (Asphodelaceae) where live under leaf bases, attended by ants. In glasshouses can be major pest.
Apterae medium-sized, oval body, orange-brown or dull green, with thin coating of flocculent wax. Antennae 5-segmented. Rostrum elongate, reaching to or beyond tip of abdomen. Apterae & alatae have trochanters fused with femora. Rounded marginal tubercles on the prothorax and abdominal segments I-VI, and very small wax glands behind each tubercle. Abdominal dorsum sparsely covered with short spines arranged in transverse rows. The trochanter is completely fused to the femur. Siphunculi absent. Alate has sclerotic bars on tergites VII & VIII and rather large marginal sclerites. Essig (1950),Song & Suh (2014)
Host alternate between pocket-like reddish-green galls on Pistacia (Anacardiaceae) and roots of grasses (Poaceae) and other plants (Ranunculus, Veronica). Not attended by ants.
Medium sized aphids, pale yellow elliptical body. Produce copious flocculent white wax. Apterae have very short 4- or 5-segmented antennae. Alatae have very short 6-segmented antennae, the third and fourth segments of which each bear a single large secondary rhinaria on the distal half. Unlike most aphids, Aploneura alatae hold their wings flat against the abdomen when at rest. Heie (1980)
Asiphonella2 spp. Iran, Pakistan, India, China, 1 now in Africa, Philippines, N&S America
Host alternate between Pistacia (Anacardiaceae), where they form large, cockscomb-like galls, and roots of grasses (Poaceae), especially Bermuda grass (Cynodon dactylon). Holocyclic in endemic areas; anholocyclic on grass roots elsewhere. Life cycle takes two years.
Dull yellowish or greenish with a coating of white flocculent wax. Antennae 6-segmented. 3-faceted eyes which are noticeably protuberant. Six wax plates on head. Rostrum short & thick, sometimes only just past first pair of coxae. Abdomen has four rows of dorsal wax plates. Cauda rounded with a few hairs Legs rather short and moderately thick. Siphunculi absent. Theobald (1923)
Baizongia1 sp. Mediterranean, Middle East, N.W. India, Pakistan, N. Africa, Kenya
Only species, Baizongia pistaceae, produces large elongate horn-like galls on primary host, terebinthus (Pistacia terebinthus (= palaestina, Anacardiaceae) & several other Pistacia spp. (P. lentiscus, P. integerrima. Secondary host is grass roots (Poaceae). In northern areas populations are anholocyclic on grass roots.
Adult apterae on roots have 5-segmented antennae have well-developed wax pore-plates, much like Aploneura. Anal aperture is dorsal (as in Geoica) with the hairs on anal plate and abdominal tergite VIII forming a trophobiotic organ to retain droplets of honeydew until removed by ants. These aphids, like for example Forda, Geoica, Paracletus,Prociphilus and some Trama, have no siphunculi. Baizongia alatae have 6-segmented antennae. Hold wings roof-like when at rest. Pterostigma has a dark central patch. Blackman et al. (2019)
Presumed to host alternate between elongate galls on leaves of Pistacia (Anacardiacae) and grass roots (Poaceae), but life cycle not yet confirmed for any species.
Emigrant alatae have ciliated secondary rhinaria. First segment of tarsi typically bears 2+3, 2+3, 2+3 (dorsal +ventral for fore, mid, hind) or 2+2, 2+2, 2+2 hairs. Groups of abdominal wax glands of alate arranged as in Geoica. Larvae deposited by emigrants devoid of groups of wax glands, bearing on each tergite only 3 pairs of hairs (one pair of very long spinal hairs, one normal pleural pair, one marginal pair of very long hairs, & one normal marginal pair. Remaudiere & Tao (1957)
Only species, Dimelaphis obtusifalcata, known from alate sexuparae collected on walnut (Juglans regia, Juglandaceae).
Head with dorsomedian suture. Alate viviparae have 6-segmented antennae; primary rhinaria circular to elliptical, secondary rhinaria semi-ring shaped, ciliated. First tarsal segment chaetotaxy 5,5,5. Pterostigma of forewing sickle-shaped, stout at apex, reaching apex of wing. Media not forked, hind wings with two obliques, separated at base. Abdominal tergites with wax plates. Siphunculi absent. Differs from other Fordinae in its forewing pterostigma being sickle shaped, stout at apex, reaching apex of wing. Zhang & Qiao (1998)
Both species in genus form branched flower-like galls on Rhus, branches thicker & rounded at apices, sometimes developing dark red spot.
Emigrant alatae rather small, with black head, pale green prothorax, dusky pterothorax and pale yellowish abdomen. Have annular rhinaria with ciliate rims. Blackman & Eastop (1982-)
Forda12 spp. Mediterranean, SW Asia, now in N America
Host alternate between leaf margin galls on pistachio (Pistacia, Anacardiaceae) to roots of grasses and cereals (Poaceae). Fundatrix lives in separate gall. Several species known only from their secondary hosts. Attended by ants on the secondary host.
Medium-sized aphids. Emigrant alates have dark head & thorax, & pale body. Apterae on the secondary host often yellowish-white & not waxy. Wax gland plates absent. Antennae of apterae & alatae 5-segmented. Antennal segment II shorter than III. Primary rhinaria without sclerotized rims, not surrounded by short hairs. Media of fore wing unbranched; bases of cubital veins slightly separated. Oblique veins of hindwing separated at bases. Blackman et al. (2019),Heie (1980)
Host alternate between globular galls at bases of leaflets of Pistacia (Anacardiaceae) and grass roots (Poaceae). Anholocyclic populations of some species in cooler climates. Complete cycle takes two years.
Small to medium-sized pale-coloured aphids. Characteristic feature of apterae is presence of fan-shaped 'spatulate' hairs as well as normal hairs. Also anus and anal plate displaced dorsally, with anal plate enlarged to form trophobiotic organ as in Baizongia. Apterae on secondary hosts have 4- or 5-segmented antennae, alatae always 6-segmented. They have no faceted wax glands. Like Forda, Baizongia, Paracletus,Prociphilus and some Trama, these aphids lack siphunculi. Alatae have variably developed dorsal abdominal cross-bands. Trophobiotic organ different from that in apterae. The anal plate and cauda are extended laterally to form sclerotized perianal ring, enclosing membranous area with anus at centre.
Form galls on Pistacia mexicana, then host alternate to roots of Asteraceae or (possibly) Ipomaea (Convolvulaceae).
Body of aptera globose probably covered with wax secretion. Head with 8 wax-glands in two longitudinal rows, thorax and abdomen with 4-6 glands per segment. Wax-glands of Pemphigine type, but without hair in the centre or a central facet as in Eriosomatinae. Head free from prothorax. Eyes of 3 ommatidia in apterae. Antennae of 5 or 6 segments, with rather long hairs. Primary rhinaria with a fringe of long hairs. Terminal process very short. First tarsal segments have 3,2,2 hairs. Siphunculi absent in apterae. Anal pore dorsal, subanal plate with a pseudocaudal projection, but cauda totally reduced. Alatae have dark brown-black dorsal abdominal cross-bands. Hille Ris Lambers (1933),Munos Viveros & Remaudiere (1999)
Inbaria swirskii produces galls on Mt Atlas mastic tree (Pistacia atlantica, Anacardiaceae) that are of irregular shape, bulbous, c. 25 mm in diameter, arising from leaf stem between bases of leaflets. Secondary hosts and other life cycle stages unknown.
Migrant alatae of Inbaria are distinguished by very large single primary and secondary rhinaria, which occupy more than half of the circumference of each segment and 0.4-0.8 of the antennal segment length. Additional characteristics are: antennal segment VI equals or is slightly longer than antennal segment III; marginal wax gland plates are invisible on abdominal tergites I-V; anal plate and cauda are laterally merged, forming perianal ring with anal aperture in the middle. Rhinaria similar to Slavum aphids, & perianal ring similar to Geoica.Barjadze et al. (2018)
In one species where the life cycle is known (Kaburagia rhusicola), host alternation is between galls on Rhus and mosses. Only one sexuparous generation matures on mosses, overwintering in an immature stage. Galls on Rhus are elongate pear- or fig-shaped, yellowish-green.
Alate emigrants are dark grey to black. Forewings with pterostigma elongated. Secondary rhinaria large, ovoid with one on each of segment III-VI; island-shaped setigerous plates present. Agarwala & Ghosh (1985)
Meitanaphis aphids gall sumac (Rhus, Anacardiaceae). Galls are jujube-like (jujube = fruit of Zizyphus) in form, up to about 4 cm long, green, becoming red or purplish when mature with many fine longitudinal ridges, with exit located at base.
Melaphis aphids host alternate from galls on sumac (Rhus, Anacardiaceae) to moss (Bryophyta). Galls globular to pyriform, largely mottled reddish-pink in colour in exposed location, pale yellow in shade.
Antennal tubercles undeveloped. Compound eyes absent in the aptera, triommatidia are present in aptera and alate. Antennae 6-segmented. The primary rhinaria have ciliate margins. Secondary rhinaria present in alatae on antennal segments III-VI. Rostrum 4-segmented. Head & prothorax fused in aptera, not in alate. Prothorax without marginal tubercles. The fore wing has reduced venation; media vein is unbranched, branches of cubitus close together at base, then divergent. Abdomen is without pigment except on last two abdominal tergites. Siphunculi absent. Cauda arc-shaped & anal plate entire. Foottit & Richards
Form inflorescence-like galls on sumac (Rhus, Anacardiaceae); galls of known species yellowish-brown, pinkish or reddish, with diameter about 5 cm. Alatae migrate in autumn to unknown secondary hosts, probably mosses (Bryophyta). Characteristics below distinguish Nurudea from very similar Schentendalia:
Emigrant alatae have yellow-green or yellow-brown abdomen. Antennal segment III similar in length to segment V with distinct annular rings; rings indistinct in segments IV & V; segment IV shortest with very large oblong rhinarium, segment V with large oval rhinarium. Stigmata of forewings much shorter, acute at tips, not sickle-like elongated. 2 obliques of hind wings very narrow, both widely separated from cubitus. Matsumura (1917)
Paracletus4 spp.
Only Paracletus cimiciformis known to complete holocycle with galls on Pistacia; emigrant alatae migrate to roots of grass (Poaceae). Sexuparae of Paracletus donisthorpei have been recorded from Pistacia terebinthus, but gall-living generations of that species so far unknown. Attended by ants.
Apterae medium-sized, yellowish or greenish All morphs have 6-segmented antennae; primary rhinaria not surrounded by rings of short hairs. Apterae have no secondary rhinaria; alatae have numerous very small secondary rhinaria scattered on underside of antennal segments III-VI. Wings of alatae are held roof-like at rest; media vein of forewing unbranched, and cubital veins leave main vein at same point. Hind wing has two widely separated oblique veins. Wax gland plates absent from all morphs. Heie (1980)
Only species, Qiao jinshaensis galls Rhus wilsonii (Anacardiaceae). Galls are yellow-green or reddish in color & inflorescence-like in shape. Possess multiple cavities & positioned at stem apex.
Antennal tubercles undeveloped. Antennae six-segmented. Rhinaria irregular in shape and numbers. Antennal segments IV-VI each have 1 large sensorium occupying most of segment, sometimes with smaller
secondary rhinaria. Rostrum reaching past front coxae. First tarsal chaetotaxy is 3,4,4. Forewing with stigma short and oblique, veins fading at their apical extremity. Abdomen has marginal and spinal wax glands. Siphunculi absent. Cauda semicircular bearing three to four hairs. Nurudea and Schlechtendalia have only 5 antennal segments, Meitanaphis has pterostigma long and sickle-shaped, Floraphis & Melaphis have numerous ring-like rhinaria, Kaburagia has only one large oval rhinarium on segments III-VI. Hebert et al. (2022)
Rectinasus1 sp. W. & C. Asia, S. Europe, N. Africa
Only species, Rectinasus buxtoni, galls pistachio (Pistacia, Anacardiaceae). Host alternates to roots of various Asteraceae where they are ant attended. Galls on pistachio are spindle-shaped sacs, 3-5 cm long, red in colour when mature. Anholocyclic populations present in some countries.
Apterae on secondary host are medium-sized to rather large, ochreous yellow to almost white, with some wax. Antennae 5-segmented, with small blunt projections on antennal segments I & II, and single rhinaria on IV & V. Rostrum has apical rostral segment long, usually about 0.67 x body, thin, black & unusually hairy.,
Abdomen has short hairs on anterior, longer ones behind. Siphunculi pore-like. Cauda rounded to cone-shaped, very hairy. Theobald (1914)
Schlechtendalia2 spp. China, Japan, Korea, Taiwan, Malaysia
Both species of Schlechtendalia host alternate between galling sumac (Rhus, Anacardiaceae) and mosses (Bryophyta). The galls are greenish-yellow to pinkish-red, densely covered with short, fine hairs, ovoid, becoming woody and irregular in shape with horn-like protrusions.
Emigrant alate has antennal terminal process very short, much less than 0.5 x base of last antennal segment. Pterostigma of forewing extends in curve around wing tip. Antenna 5-segmented; II-V each with at least partial separation of the sensoriated surface into smaller units. Siphunculi absent. Related to Melaphis, but they do not have an elongate curved pterostigma. Blackman & Eastop (1982-)
Producing sac-like or coral-like galls, often reddish when mature, on Pistacia (Anacardiaceae). Emigrant alatae thought to host-alternate, but secondary hosts unknown. One species only found on Pistacia.
Antennae of apterae are 5-segmented with secondary rhinaria on segment V. Eyes are triommatidia. Rostrum reaches past middle coxae. First tarsal segments have 3 hairs. There are spinal and marginal wax glands on the thoracic and abdominal tergites I-VII. Antennae of alatae 5-6 segmented. Abdomen has pigmented transverse spinal waxbands on some tergites. Closely related to Aploneura.Blackman & Eastop (1982-)
In warm countries, Smynthurodes betae is heteroecious holocyclic, host alternating from galls on Pistacia (especially P. atlantica) to roots of many dicotyledonous plants. In cooler climates, anholocyclic populations present on secondary hosts. Fundatrix produces small midrib galls for self, & larger leaf-edge galls for offspring. Galls yellow-green or red, spindle-shaped, about 2 cm long.
Emigrant alatae have 6-segmented antennae. Antennal segment VI not longer than segment III. All rhinaria with broad sclerotized rims. Abdominal tergites I-V without marginal wax glands. Apterae on secondary host rather small. Second segment of the antenna is distinctly longer than first, being similar in length to third segment; terminal process is less than 0.5 x base of last segment. Body & appendages densely hairy. No siphunculi. Blackman et al. (2019)
Both Tramaforda species form flat galls on the margins of leaflets of primary host Pistacia atlantica. Emigrant alatae leave galls in October for unknown secondary host.
Emigrant alatae have antennae 5-segmented. Abdominal tergites I-V without marginal wax glands. Embryos in migrant alatae with elongate hind tarsi. Sexuparae large, with long rostrum and elongate hind tarsi. Manheim (2007)
Only species, Ceratopemphigus zehntneri, produces galls on privet (Ligustrum, Oleaceae), especially tree privet (L. robustum) and Chinese privet (L. chinense). Also observed on Brunfelsia uniflora (Solanaceae) (accidental?). Galls on stem are bulbous, bright green initially, maturing to brown-grey. Life cycle not known.
Antennae of adult alatae 6-segmented. Small conica protuberance at base of antennal segment II. The primary rhinarium has long hairs, and secondary rhinaria have short hairs. Apical rostral segment is wedge shaped. Dorsal wax of adult aphids is well developed. Femur & trochanter are fused. First segment of tarsus has 2,2,2 hairs. Siphunculi absent. Immatures of III-IV instar with pair of obvious finger-like protuberances on top of head. Protuberances almost disappear in adults. Related to Prociphilus, but frontal protuberances in immatures Hormaphidinae-like. Qiao & Fang (2007)
Clydesmithia canadensis first reported galling leaves of Populus (balsamifera, trichocarpa) (Salicaceae); galls elongate slightly wrinkled swelling on leaf lamina, tinged with red. Immatures of third generation drop to ground to colonise roots. Then reported to host alternate migrating to conifer roots and mosses. Life cycle still unclear.
Fundatrices on Populus with 4-segmented antennae, and without wax glands. Apterae in galls yellowish with thin layer of wax. Apterae on conifer roots with short, 5-segmented antennae, segment V longest, with short terminal process. Rostrum extends to metacoxae, apical rostral segment with subapical pale zone, without accessory hairs. Number of hairs on first tarsal segments 2,2,2. Hairs on body and antennae sparse, very short. Dorsum smooth, with indistinctly visible dorsal wax glands. Thought to be related to Pachypappa and Gootiella.Danielsson (1990),et al. (2012)
Cornaphis populi produces galls on Populus angustifoli (Salicaceae). Galls are crescent-shaped folds of the leaf-edge, pale green often streaked with red, usually only 1 gall to a leaf. Cornaphis are monoecious holocyclic, with 4 generations on poplar: fundatrix, fundatrigeniae, sexuparae and sexuales.
Wax plates absent in fundatrix, but present in apterous fundatrigenia. Antenna of fundatrix 5-segmented, of fundatrigenia, 6-segmented. Permanent rhinaria ciliated. Head has medial frontal projection forming distinct horn in apterae. Alate sexupara has raised base for the median ocellus. Fundatrix, fundatrigeniae and (alate) sexuparae all develop in gall together. Gillette (1913)
Only species, Diprociphilus allivorus, feeds on victory onion (Allium victorialis, Amaryllidaceae). Life cycle unknown.
Apterae medium sized, yellowish white, most likely wax covered. Antennae 5-segmented. Primary rhinarium with long cilia. Rostrum reaches abdominal segment IV, with apical rostral segment 1.5 x second hind tarsal segment, with 2 accessory hairs. Tarsi 2-segmented. First tarsal segments have 2,2,2 hairs. Related to Prociphilus, but that genus has much shorter rostrum. Qiao et al. (1999)
Produce galls on primary host, poplar (Populus, Salicaceae). Galls usually reddish or yellowish, elongate often caterpillar-like. Where known, host alternate to roots of Asteraceae, Polygonaceae, Balsaminaceae.
Fundatrix with 4-5 segmented antennae, without wax glands, without
siphunculi, with empodial hairs very short; embryos inside fundatrices also with short
empodial hairs, with wax glands. Alatae of second generation with minute, unpigmented, nearly invisible siphunculi, usually with unbranched media in the fore wings, secondary rhinaria with very distinctly
ciliated rims, and very irregular chaetotaxy of first tarsal joints. Resemble Pachypappa in fundatrices with no wax pore-plates; resemble Pemphigus in unbranched media vein & first instar exules with short empodial hairs. Hille Ris Lambers (1966)
Only species, Formosaphis micheliae, feeds on bark of magnolias (Michelia, Magnolia, Magnoliaceae). May have Populus as primary host, or be entirely anholocyclic.
Alatae have antennal tubercles absent. Antennae short, stout, 5-segmented, almost without hairs, with extensive reticulated sensory area on each of segments III-V; terminal process very short. Fore
wings with pterostigma not elongate; hind wings with 2 obliques. Abdomen with wax-plates. Body provided with a few bristles which are not capitate, without dorsal tubercles. Siphunculi absent. Cauda not distinct. Anal plate rounded. Tarsi normal. Aptera much as alate except covered with cottony wax, eyes are triommatidia, antennae 4-5 segmented without secondary sensoria, & abdominal segment VII with small blunt tubercle on the side. Takahashi (1925)
Both species gall their primary host poplar (Populus, Salicaceae), forming yellowish bag-like or conical leaf galls. Aphids live in dense wax-covered colonies on the lower side of the leaf-cone. Secondary host likely to be roots of Juniperus. Overwintering as parthenogenetic apterae may be commoner than (sexual) egg production.
Fundatrix has wax gland plates on head as well as on thorax & abdomen. Emigrant alatae are greyish green, clothed with wax. Antennae are 6-segmented, with secondary rhinaria on segments III & IV. Segments V & VI each have a large primary rhinarium, the edge of which has finger or star-shaped protrusions. They are not surrounded by distinct rings of short hairs. (1980)
Only species, Grylloprociphilus imbricator, has American beech (Fagus grandifolia, Fagaceae) as its primary host on which it forms large waxy colonies; migrates to roots of bald cypress (Taxodium distichum, Cupressaceae).
Fundatrix has distinctive wax plates. Emigrant alatae have 6-segmented antennae, bearing oval, ciliated secondary rhinaria. Fore wings have simple media vein. Hind wings have media and cubitus originating near the same point. Hind femora on the sexuparae are distinctly larger than the pro- or mesofemora. Cauda rounded & indistinct. Differs from Pemphigus,Prociphilus & Stagona in having hind femora enlarged. Differs from Pemphigus in having more hairs on the apical rostral segment (RIV+V) and in having secondary rhinaria with long cilia. Grylloprociphilus differs from Prociphilus & Stagona in having spine-like setae at apex of tibiae. Smith and Pepper (1968)
Mimeuria ulmiphila, makes a terminal leaf-nest pseudogall on maple (Acer campestre,Acer platanoides, Aceraceae) host alternating to roots of elm (Ulmus laevis, Ulmus ocera, Ulmaceae). However, anholocycly on Ulmus roots predominates in some countries.
Only species is Mimeuria ulmiphila. Emigrant alatae rather large, dark brown. Antennal terminal process on both winged and wingless adults vestigial, less than 0.1 x base of last antennal segment. Apterae on roots of secondary host are medium-sized, yellow, thickly wax-powdered, and encased singly in brown mycorrhizal cysts. They have one-segmented tarsi. Related to Prociphilus subgenus Paraprociphilus.Heie (1980)
Mordwilkoja1 sp. orig N. America, now also Europe, Asia
Mordwilkoja vagabunda produces galls on poplar (Populus acuminata, Populus deltoides, Salicaceae). Galls are large, irregular, bladder-like growths. Emigrant alatae migrate to roots of secondary host, loosestrife (Lysimachia, Primulaceae).
Alatae have antennal tubercles undeveloped. Antennal segment II about 1.4 x longer than segment I. Secondary rhinaria annular. Antennal terminal process longer than base antennal segment VI, & with characteristic clear spots of unknown function. Forewing media vein unbranched, hindwing has two cross veins with bases joined or nearly joined. Siphunculi are absent or obscure, cauda rounded. Mordwilkoja similar to Pemphigus, but that genus has antennal segment II roughly equal to segment I. Pike et al. (2003)
Neopemphigus turajevi live in dense wax-dusted colonies causing gall-like swellings on fine roots of Boll's poplar (Populus bolleana = Populus alba 'Pyramidalis').
Emigrant alatae with antennal segments III & IV each bearing single subapical secondary rhinarium, like the primary rhinaria on V & VI. Secondary rhinaria with ciliated rims. Forewing with media unbranched. Closely related to Pachypappa.Blackman & Eastop (1982-)
Monoecious on podocarps (Podocarpaceae) and araucarians (Araucariaceae). Sexual morphs often occur in mixed colonies with parthenogenetic morphs in spring, summer or autumn.
Apterae orange-brown to purplish, waxed on posterior segments. Alatae with copious tendrils of white wax. Antennal tubercles undeveloped. Antennae 6-segmented, with semi-annular secondary rhinaria; primary rhinarium has hairy fringe. Eyes of apterae are triommatidia. Head and pronotum more-or-less fused in aptera. In alate fore-wings have the media vein twice branched; hind-wings have both the media and cubitus present. Siphunculi very small, much wider than long. Cauda somewhat elongate and knobbed. Anal plate slightly divided. Oviparous females may be winged, and possess semi-annular secondary rhinaria. Pike (2003)
Host alternate between pseudogalls on poplar (Populus, Salicaceae) and the roots of spruce (Picea, Pinaceae).
Medium-sized aphids with large fundatrices; fundatrices have no wax glands. Antennal tubercles undeveloped. Alate viviparae rather large, greenish, reddish or brownish. Antennae with oval to oval transverse rhinaria. Forewings with once-branched media vein. Hindwing with 2 obliques with bases joined or nearly joined. Body with many fine hairs. Siphunculi absent. Pike (2003)
Primary host is aspen (Populus tremula, Salicaceae). Gall formed by folding down leaf lamina to form cone, which becomes bright orange. Migrate to roots of Norway spruce (Picea abies, Pinaceae). Root-feeding yellowish apterae live in nests of dense wax wool. May also feed on moss? May overwinter anholocyclically on Picea roots.
Fundatrices very large, greyish brown with white wax. Wax gland plates present on fundatrices & alatae on thorax & abdomen, not head. Emigrant alatae rather large, greyish brown. Antennae 6-segmented, about 0.4 x body. Secondary rhinaria on segments III & IV. Siphuncular pores rather large. Closely related to Pachypappa.Heie (1980)
Patchiella2 spp. Europe, Japan, now in India, China, Pacific is & USA
Both species of Patchiella host alternate between lime trees (Tilia, Malvaceae) and the roots of arums (Araceae). Fundatrix lives in a compact leaf-nest pseudogall, formed by twisting and stunting the epicormic shoots of Tilia. Ant attended.
Fundatrices are very large, blackish-green or reddish-brown. Rostrum thin and acuminate, pale
at base, dark on apical half, reaching just past base of second coxae. Siphunculi absent. Emigrant alatae may have forewing media branched (Patchiella reaumuri) or unbranched (Patchiella kolokasia). Blackman et al. (2019)
Primary host is poplar (Populus, Salicaceae) where fundatrix induces galls on leaves, petioles or branches. The secondary host is a herbaceous plant where they form colonies on the roots or in a woolly wax mass above soil level. Not attended by ants.
Pemphigus are small to medium-sized yellowish-green or greyish-green aphids which live in galls on the leaves, petioles or branches of their primary host. Fundatrices in galls have short 4-segmented antennae, and spinal, pleural and marginal wax glands on most body segments; wax glands absent from head. Winged viviparae that emerge from galls have black head & pterothorax, & rather elongate greenish wax-dusted abdomen. Antennae have relatively long last segment, longer than segment V, usually bearing secondary rhinaria, & primary rhinarium is enlarged and fringed with hairs. Heie (1980)
Prociphilus50 spp. N hemisphere, 2 now in Australasia, Africa, S America
Prociphilus have recently transferred their sexual generation from Populus to various 'more advanced' primary hosts in Rosaceae, Caprifoliaceae and Oleaceae where they live as waxy clumps. Like the related Pachypappa, secondary hosts have remained unchanged as roots of conifers.
Rather small to very large aphids. Primary rhinaria surrounded by short hairs. Media of forewing unbranched. Tarsi & tarsal claws relatively long. Wax gland plates present on head, thorax and abdomen, even in fundatrix, producing copious wax. Siphuncular pores small or absent. Heie (1980),Blackman et al. (2019)
Thecabius19 spp. N America, England to Japan, 1 also in N Africa
Most species dioecious holocyclic. Primary host poplar (Populus, Salicaceae) where aphid induces gall; fundatrix produces small 'fundatrix' gall, offspring induce separate 'whole leaf' gall. Secondary host is roots or stems of buttercups (Ranunculus: Ranunculaceae) and Lysimachia (Primulaceae). Not attended by ants.
Small to medium-sized aphids. Fundatrix with 5- or 6-segmented antennae; other morphs usually with short 6-segmented antennae All morphs have wax gland plates, in apterae placed in 4-6 longitudinal rows producing a dense covering of wax spicules; sometimes fundatrix & apterous viviparae on secondary host also have wax plates on head. Emigrant alatae have 2-5 hairs on first tarsal segments with 3 or more hairs on at least some tarsi. Siphuncular pores present. Heie (1980)
Tiliphagus lycoposugus produces large clumped leaf nest galls on primary host, American basswood (Tilia americana, Malvaceae). Alatae migrate to roots of water horehound (Lycopus virginicus, Lamiaceae).
Fundatrices in galls large, brown, globose; emigrant alatae reddish brown; apterae on roots white to flesh-coloured, with wax. Antennae 5-segmented in fundatrix, 5-6-segmented in apterous vivipara, 6-segmented in alatae. Primary rhinarium with cilia, secondary rhinaria narrow, elongate, very numerous. Media of forewing usually simple. Hindwing with 3 veins, originating near common point. Tarsal chaetotaxy of offspring of fundatrix variable; apterous summer vivipara 3,2,2. Siphunculi absent. Cauda rounded, bearing numerous hairs. Similar to Prociphilus, but Tiliphagus has many more secondary rhinaria. Smith (1965)
Only species Uichancoella gabrieli feeds on stone oak (Lithocarpus, Fagaceae). Life cycle unknown. Originally described as member of Pemphigini, where it is covered by Favret, but considered by Blackman to be member of Nipponaphidini. Apparently related to Schizoneuraphis.
Apterae rather small, blackish-brown profusely covered with white wax, leaving only centre of dorsum exposed. Prosoma with marginal hairs very long, stout basally but with finely-pointed apices, with 5 pairs of similar large spino-pleural hairs. The 3 thoracic tergites also bearing several somewhat shorter, thinner hairs. Blackman & Eastop (1982-)
Anomalaphis comperei feeds on peppermint (Agonis flexuosa), A. casimiri on tea tree (Leptospermum) (both in Myrtaceae). Monoecious holocyclic.
Rather small aphids, brown or greyish green. Antennae of both apterae and alatae 5-segmented with subcircular secondary rhinaria. Forewings with the media once branched; hind wings considerably reduced, with the cubitus absent. Abdominal tergites VII and VIII each bear slender hair-bearing processes. Siphunculi cylindrical or tapering (distinctly swollen in earlier descriptions), with a ring of 3-8 hairs on the distal half; with or without polygonal reticulation on siphunculi. Cauda broadly rounded. Baker (1920)
Anomalosiphum9 spp. India to Japan to Papua New Guinea
Probably monoecious holocyclic on woody, mostly shrubby Connaraceae, Fabaceae (especially Dahlbergia) and Xanthophyllaceae. Most species biology unknown.
Rather small to medium sized, dark brown or greenish where known. Antennae 4-segmented in apterae, 5-segmented in alate viviparae; with terminal process shorter than base. Secondary rhinaria on flagellar segments of alate antennae semiannular. Each of abdominal tergites VII & VIII have a pair of pronounced hair bearing processes in apterae; these reduced in alatae and usually only distinguishable on tergite VIII as large hair-bearing tubercles. Siphunculi large, much longer than wide. Cauda transversely rounded-triangular, with a pronounced median stylus in apterae, which is reduced in alatae. In only species where sexuales known, both oviparae & males alate. Takahashi (1934),Martin & Agarwala (1994)
Only species is Brasilaphis bondari. Sampled in water trap so host unknown.
In apterae, head does not seem to be separated from prothorax. Eyes are triommatidia. Antennae 5-segmented or rarely 4-segmented. On end of abdominal tergite VII there are two processes protruding hindwards. Alatae fold wings rooflike. Wing veins fuscous bordered (see here. Alatae have antennae 5-segmented, with secondary rhinaria on segments III & IV. First tarsal segments with 5 hairs. Forewing media vein two branched, hind wings narrow & rudimentary with only one longitudinal vein. Abdomen has transverse sclerotized bands on posterior segments. Siphunculi with hairs; slightly swollen & outcurved. Mordvilko (1930)
Feed on variety of trees and shrubs, especially in the Tiliaceae, Fagaceae, Malvaceae, and Fabaceae. Sexuales only recorded for one species. Cervaphis rappardi regarded as important pest of pigeon pea in India.
Rather small aphids, yellowish or greenish. Characterised by presence, in apterae, of long branched marginal hair-bearing processes on head, thoracic & most abdominal segments. Antennae 4-5 segmented, with terminal process 1.0-1.5 x base antennal segment VI. Prothorax fused with the head. Tergite VIII has a plate with 5-10 hairs, the two middle hairs on a process. Siphunculi long, cylindrical, slightly curved outwards and a little swollen subapically, where there is a ring of small hairs. Cauda with has 6 hairs with a median process. In alatae processes are reduced to low, flat hair-bearing tubercles, except on head. Hille Ris Lambers (1956),Noordam (1994)
Only species, Meringosiphon paradisicum, known to feed on Gastrolobium dilatatum & (possibly) Daviesia divaricata (both Fabaceae). Life cycle unknown
Apterae medium sized, probably brownish with black siphunculi, adorned with long hairs sited on low tubercles. Head with low frontal tubercles. Eyes compound with triommatidia. Antennae 6-segmented in apterae & alatae. Primary rhinarium not ciliated, alatae with secondary rhinaria on segment III. Wing veins fuscous bordered. Forewings with twice-branched media. Siphunculi more or less cylindrical, with hairs on basal half & subapically. Cauda crescent shaped, shallow & broad. Carver (1959)
Sumatraphis2 spp. India to China to Sulawesi, Sumatra & Sulawesi
Feed on Nilgiri elm (Celtis tetrandra) & (possibly) Trema orientalis (both in Cannabaceae). Life cycle & sexual morphs unknown. Apterae are flattened into angles of new shoots.
Apterae medium-sized, yellow, green or brown. Antennae 4-segmented in apterae, 5-segmented in alatae. Secondary rhinaria strongly protuberant. Spiracles distinctly protruding. Marginal processes on abdomen gradually becoming longer towards the cauda, each bearing 3-4 hairs and one sharp spine. Dorsal cuticle corrugated. Dorsal process on tergite VII conspicuous. Siphunculi elongate, swollen apically on inner margin. Forewings with media once branched, hind wings with both obliques. Ghosh (1982)
Feed on oak (Quercus spp.), chinquapin (Castanopsis hicklii) & bamboo-leaved oak (Cyclobalanopsis neglecta = Quercus bambusifolia). Produces sexuales but life cycles not fully known
Apterae medium-sized, probably green nor brown, with very long siphunculi. Median frontal tubercle distinct. Antennae much shorter than body, 5 or 6 segmented, with some long capitate hairs. Body narrow, not strongly sclerotized, pale. Hind tibiae with spinules scattered on distal part, without ridges. First tarsal segment chaetotaxy: 7,7,7. Abdominal segments III-VI fused together. Dorsal hairs not numerous, distinctly capitate. Siphunculi very long, slender, not reticulated, with spinules on apical and basal parts and many long hairs. Cauda rounded at apex. Differ from Eutrichosiphum in presence of distinctly capitate or spatulate hairs. Qiao (2000) For picture see here.
Most species feed on members of Fagaceae, but some from other families (e.g. Betulaceae, Elaeocarpaceae, Lauraceae, Apocynaceae, Euphorbiaceae). Monoecious holocyclic with alate oviparae & males.
Apterae medium-sized, with elongate oval or pear-shaped body, usually yellow or greenish, sometimes dark. Antennae 5-segmented, with long hairs and somewhat oval rhinaria. Long, tapering and distinctly subdivided apical rostral segment. Hind tibiae without stridulatory ridges. Siphunculi very long, more or less cylindrical, covered with hairs & without any reticulation in apterae. Cauda without a median process. Alatae have forewings with media twice branched, hind wings with both media and cubitus present. Baker (1920),Blackman & Eastop (1982-)
Greenidea61 spp. Pakistan to Japan to Java, 2 now near worldwide
Greenidea feed on twigs and undersides of leaves of various trees. Some species mainly or entirely anholocyclic, others produce sexuales. Greenidea psidii & Greenidea ficicola introduced to many other countries.
Apterae medium sized, usually brown or yellowish green. Antennae 6-segmented. Fore wing has media vein twice branched, and radius curved; hind wing has two oblique veins. Tibiae have 4 distinct spines, and first tarsal joints have 7 hairs. Abdominal tergum mostly sclerotic, pale to blackish brown with many stiff hairs with serrated or branched apices. In apterae siphunculi curved outwards, narrowing to the base and to apex. In alatae siphunculi more cylindrical on the basal half, curved outwards at the apex. Siphunculi always covered with long hairs. Subgenus Greenidea have reticulations covering most of siphunculi; Trichosiphum has reticulations only at base. Cauda more or less semicircular with style-like process at apex. Noordam (1994)
Feed on plants in several different families, especially ironwood (Mesua, Calophyllaceae) & Bridelia (Phyllanthaceae). Host plants of several species unknown.
Medium-sized elongate, mostly green, yellow or brown. Antennae 5- or 6-segmented with spinulose basal segments. Apical rostral segment short & obtuse, no clear division between RIV & RV. First tarsal segments with 7,7,7 or 5,5,5 hairs. Abdominal tergum mostly sclerotic, rather pale; dorsal hairs thick and stiff, scarce, & blunt. Siphunculi have no reticulation, are curved abruptly outwards near apices, & covered with spinules. Cauda rounded triangular or semicircular, without stylus-like process. Alatae distinctive, with elongate, dark pterostigma, media only once-branched, hind wings reduced, without oblique veins. Raychaudhuri (1956),Blackman & Eastop (1982-)
Two of three species feed on trees in Fagaceae (stone oak, Lithocarpus bennettii; chinquapin, Castanopsis hainanensis); other found on Premna odorata (Lamiaceae).
Apterae rather small to medium-sized, pear-shaped. Eyes with multi-facets and ocular tubercle. Antennae 4-segmented in apterae, 5-segmented in alatae. First tarsal segments with 5 hairs. Prothorax fused with head. Body with sparse, blunt, mostly short hairs; alatae also have very short hairs but acute, not blunt. Siphunculi 0.19-0.25 x body length, with convex inner side, enlarged in median part, over 20 stout long hairs, little or no reticulation, but with spinulose imbrication. Single described alata has twice-branched media and hindwings with one oblique vein. Noordam (1994),Zhang & Qiao (2008)
Mollitrichosiphum18 spp. India to Japan to Philippines & Java
Colonize young leaves and branches of plants belonging to several families, mostly Fagaceae or Betulaceae (Alnus), but also many others. Only few sexual morphs recorded, most species seem to have some anholocyclic populations.
Apterae rather large, usually elongate with very long siphunculi. Median portion of frons flat. Antennal tubercles only slightly developed. Antennae 6-segmented. In alatae numerous secondary rhinaria on antennal segment III. Media vein of the fore wing twice branched; hind wing with two oblique veins. First tarsal chaetotaxy 7,7,7. Aptera with numerous transverse ridges on hind tibia. Underside of abdomen spinulose, with two distinct elongated areas of dense spinulosity postero-laterally. Siphunculi cylindrical, elongated, densely covered with spinules. Cauda & anal plate rounded or transversely oval. Zhang & Qiao (2010)
Only species, Tritrichosiphum thailandicum, feeds on gurtjuntree (Dipterocarpus tuberculatus, Dipterocarpaceae). Apparently not recognised by Blackman in AWP.
Apterae rather small, dark green to brown. Entire body covered dorsally & laterally with minute spinules. Antennal tubercles small. Triommatidium almost as large as compound eye. Antennae 4-segmented, without secondary rhinaria. Rostrum long and slender, with apical rostral segment in two distinct parts, RIV & RV, and very slender. First tarsal segments with 3 hairs. Siphunculi with spine like hairs, & unusually marked basal constriction; no reticulation, but spinules as on rest of body. Cauda semioval, with no median process. Tritrichosiphum considered closest to Eutrichosiphum.Robinson (1972)
Hosts include lavender croton (Croton subgratissimus) & unidentified Euphorbia spp. (Euphorbiaceae). Sexuales have been found for one species. Most likely monoecious holocyclic. Ant attended.
Apterae rather small, where known oval, somewhat flattened, brownish yellow or blackish green. Head has two pairs of spinal processes. Antennae 5-segmented, with terminal process longer than base segment V.
Spinal processes also present on all segments to abdominal tergite VII, and marginal processes at least from abdominal tergites IV & VI. No hairs on basal half of marginal process on VII, but present on III & IV. Pleural hairs very small, and irregularly present on tergites I-V. Siphunculi fairly long & conical. Remaudiere (1988)
Only species, Paulianaphis madagascariensis, lives in galls on leaf of dogbane (Apocynum, Apocynaceae).
Apterae medium-sized, broadly oval, with head, antennae, legs, siphunculi & processes on tergite VIII black. Antennae 5-segmented; primary rhinaria on segments IV & V with thick, non-ciliated margin. Rostrum short, not reaching posterior coxae. Second tarsal segment with empodial hairs spatulate. Spiracular openings exceptionally large. Abdominal tergite VII bears one pair each of marginal & spinal processes. Siphunculi short, with very broad bases & conical apical part. Cauda bears 8 hairs. Alatae have thickly-bordered forewing veins. Related to Eonaphis and Schoutedenia, but has processes & different host association. Ghosh (1982)
Both currently recognised species monoecious holocyclic on woody Phyllanthaceae. Still uncertain whether two current species are distinct. Ant attended.
Apterae medium sized, yellow-green. Frontal tubercles absent. Antennae 5-segmented. Apterae without secondary rhinaria; alatae with secondary rhinaria on segments III & IV. Eyes are triommatidia. Prothorax fused with head. First tarsal segments have 3 hairs. Abdominal tergites I-VIII reticulated. Siphunculi are cones with concentric imbrications. Tergite VII has two pale brown processes pointing backwards, & tapering gradually from base to apex. Cauda without median process, bears 4 hairs. Noordam (1994)
Wide range of host plants, especially in Asteraceae, but also in Balsaminaceae, Poaceae, Moraceae, Plantaginaceae, Scrophulariaceae, Styracaceae, Theaceae, Verbenaceae and Violaceae. Five species may be anholocyclic; two species gall leaves of primary host, but secondary hosts are unknown.
Rather small to medium-sized oval, flat, scale-like aphids, variably coloured black, brown, reddish. Apterae have aleyrodiform body with no frontal horns. Head & prothorax fused, as are meso- and metathorax. Antennae 4 or 5-segmented, with primary rhinaria small & ciliated. Eyes are triommatidia. Wax glands arranged along crenulated margin of body. Abdominal tergites I-VII also fused, only tergite VIII free. Dorsal hairs fine and sparse. Siphunculi ring-shaped. Cauda knobbed. Anal plate bilobed. Similar to Cerataphis aphids, but Cerataphis have frontal horns and lack clear division between prothorax and mesothorax. Alatae have 5-segmented antennae with near ring-shaped secondary rhinaria. Jiang & Qiao (2011)
Astegopteryx26 spp. India to Taiwan to Java to Tonga
Some species dioecious holocyclic in parts of their distribution, host alternating between galls on snowbells (Styrax, Styracaceae), and monocots, specifically palms (Arecaceae) and bamboos (Poaceae). Morphs in galls may differ greatly from same species on secondary host.
Apterae in galls usually wax-covered. Emigrant alatae with 5-segmented antennae; segments III-V bearing ring-shaped annular secondary rhinaria. Wings held horizontal at rest (hence the name Astegopteryx). Apterae on secondary host yellow or grey with coloured pattern. Variably waxed, from wax fringe along body margin to completely covered with wax. Head has 2 horns dorsally. Antennae rather short, with 4-5 segments Eyes are triommatidia. Apical rostral segment short. Prothorax is fused to the head, and the body has a furrow posterior to pronotum. First tarsal segments have 2-4, 2-4, 2-3 hairs. Siphunculi cone-shaped, colourless or brown. Cauda transversely elongate with knob & constriction. Noordam (1991)
Cerataphis10 spp. India to Taiwan to Java, a few now in Europe, N&S America, Australia
In Asia three species host-alternate between galls on snowbells (Styrax, Styracaceae) and secondary hosts in the palms (Arecaceae), orchids (Orchidaceae), screw palms (Pandanaceae), and bamboos (Poaceae). Some species like Cerataphis orchidearum have anholocyclic populations in areas outside their natural range.
Apterae living in galls on primary host have a thick covering of wax. Some immatures are soldiers which defend the gall. Emigrant alatae have the head without horns. Antennae are 5-segmented with annular secondary rhinaria on segments III-V. Apterae on the secondary host (form most commonly observed) are dull or shiny brown, oval in shape with a transverse furrow in the middle, and a flat horizontal white fringe around the body. Ventral to the frontal wax glands are two horns, smooth, acute without hairs. Antennae have 4 or 5 segments. The eyes are triommatidia. Dorsum is sclerotic & free from tergite VIII. Abdominal tergites I-VII are fused, with at least 30 wax glands on each side. Siphunculi are situated dorsally, without distinct border. Cauda transversely elongate with constriction. Noordam (1991)
Two species host alternate from snowbells (Styrax, Styracaceae) to bamboo (Poaceae) (although some populations anholocyclic on bamboo). Two species only known as anholocyclic on bamboo. One species remains all year on Styrax, one on Camellia (Ceaceae), and one anholocyclic on Phragmites communis (Poaceae). On primary host, aphids form peculiar, multiple-cavity galls.
Emigrant alatae have two blunt horns on the head, shorter than in apterae. The antennae are 5-segmented, with secondary rhinaria on segments III -V. Apterae on secondary host have white fringe of wax. The head is fused to the pronotum. The head has two horns, with sharp or rounded points. The antennae have 4-5 segments, & eyes are triommatidia. The mesonotum, metanotum & abdominal tergites VII & VIII are distinctly defined, other segments marginally fused, but with furrows dorsally. No wax glands on head, but there are wax glands on thoracic segments and abdominal segments I-VI. Siphunculi located on segment V, with 3-11 hairs. Cauda without a constriction. Noordam (1991)
Ceratovacuna25 spp. India to Japan to Java, 1 also in Fiji & Solomon Islands
Thought to host alternate between Styrax (Styraceae) and grasses (Poaceae), although this only confirmed for two species, many populations may be anholocyclic. Produce multiple-cavity galls on primary host. Some species have horned first instar soldiers. Closely related to Astegopteryx.
Emigrant alate with black head & thorax, abdomen yellowish, brown or black. Head has two frontal horns. The antennae have 4-5 segments, & bear annular secondary rhinaria on segments III-V. Apterae on secondary host are yellow, brown or black, the margins with white wax cones, or whole body densely covered in wax. Head fused to pronotum, but remaining thoracic and abdominal segments not fused. Head has two horns, usually triangular with sharp points, & may, or may not, have wax glands. Antennae have four or five segments. Eyes are triommatidia. Marginal wax glands present on thoracic and abdominal segments in most species. Siphunculi on segment V, with ring around the pore, elevated slightly above the surface. Cauda transversely elongate, with knob and constriction. Anal plate bilobed. Noordam (1991)
In large colonies on undersides of leaves of bamboos, (Bambusa, Arundinaria, Phyllostachys, Yushania, Poaceae). Life cycle unknown.
Apterae medium-sized, body round, flat, & strongly sclerotized, yellowish-brown to dark purple to violet-black, covered with fine wax powder. Head with 1 pair of frontal horns, cylindrical with broadly rounded tips, nymph with blunt frontal horns from birth. Head plus pronotum, meso- and metanotum, and abdominal tergites I and VIII mutually free, other abdominal tergites completely fused. Eyes with 3 facets. Antennae 4- or 5-segmented. Rostrum short and thick. Ultimate rostral segment blunt, wedge-shaped. First tarsal chaetotaxy: 4,3,2. Dorsum with irregularly shaped wax facets, sometimes wax plates in groups along the abdominal margin. Siphunculi pore-like, not on hairy cones. Cauda knobbed and constricted at base. Anal plate bilobed. Hille Ris Lambers & Basu (1966),Wang & Huang (2024)
Glyphinaphis1 sp. Assam, India, China, Japan, Singapore, Java, Sulawesi
Only species, Glyphinaphis bambusae, can be found scattered on young shoots or at leaf bases of bamboos (Bambusa, Shibataea, Dendrocalamus, Indocalamus, Phyllostachys, Pleioblastusamarus, Schizostachyum, Poaceae).
Apterae are small pale olive green to reddish or greenish brown, somewhat shiny aphid. Head without frontal horns. Antennae 4-segmented; alatae with linear secondary rhinaria on segment III. Eyes triommatidia. Fore wings with media once branched; hind wings with both media and cubitus present. Dorsum covered with stout spine-like hairs. Wax gland plates reduced to groups of minute wax pores. Siphunculi present as mere pores. Cauda knobbed. Anal plate rounded. Immatures spotted Alatae have bluish black abdomen. Baker (1920),Noordam (1991)
Ktenopteryx1 sp. Guanxi Autonomous Region, Fujian Province, China
Only species, Ktenopteryx eosocallis feeds on young shoots, and undersides of leaves along the main veins, of snowberry (Styrax odoratissimus & other Styrax species). Causes stunting of shoots and leaf deformation. Life cycle unknown.
Apterae small, oval, yellow or yellowish brown, with strongly sclerotized body. Head fused with prothorax, mesothorax to segment VII fused with each other, segment VIII free. Eyes triommatidia. Antennae 4-segmented. Apical rostral segment wedge-shaped. There are 2,2,2 hairs on first tarsal segments. Dorsum of body covered with C or O shaped wax plates. Has curved blunt-ended frontal and marginal processes. Tergite VIII has 1 long cone-shaped process arising from posterior margin of tergite. Dorsal hairs of body short and stout at apices. Siphunculi pore-like segment V. Cauda knobbed with 4-6 hairs. Anal plate bilobed. Qiao & Zhang (2003)
Produce multiple-cavity galls on primary hosts snowbells (Styrax, Styraceae). Secondary hosts are bamboos & grasses (Poaceae), or ginger (Zingiberaceae). Produce sterile second-instar soldiers on primary host & large sterile first-instar pseudoscorpion-like soldiers on secondary hosts. Dioecious holocyclic, but some anholocyclic populations on secondary hosts.
Emigrant alatae from galls have 5 antennal segments, with secondary rhinaria on segments III-V. Apterae on secondary host have medium-sized oval-shaped body, wax-tufted or wax-dusted. Much of body covered with denticles. Head has two blunt, or sharp, conical frontal horns. May have two pleural grooves on their pronotum. Antennae 4- or 5-segmented. Rostrum short, not reaching second coxae. Wax glands present on thoracic segments. Abdominal dorsum with numerous small dark scleroites bearing fine hairs, & large marginal sclerites. Siphunculi circular, slightly elevated on narrow sclerotic cones. Tergite VIII with transverse sclerotic patch & long fine hairs. Cauda transversely elongate with knob. Anal plate bilobed. Most closely related to Ceratovacuna apterae, but they have no obvious pleural grooves. Aoki & Kurosu (2010),Noordam (1991)
Tuberaphis17 spp. India to Japan to Java & Papua-New Guinea
Most species host alternate between their often elaborately-branched galls on Styrax, and secondary hosts in Loranthaceae or Santalaceae. Some species remain on Styrax all year.
Apterae medium sized, have many well-developed wax-plates arranged in row around body (other than between antennae) providing wax fringe. Head short, fused with the prothorax, with 3 prominent blunt tubercles on the front. Eyes triommatidia. Antennae short, 5-segmented with short terminal process. Pronotum distinctly defined from the mesonotum. Meso- and metanota somewhat defined, basal abdominal segments fused together. Tergite VIII separate. Legs rather short; tarsi have 2 long knobbed hairs. Siphunculi very short, mere rings. Cauda constricted basally. Anal plate divided. Tuberaphis closely allied to Cerataphis, but Cerataphis have wax plates between antennae, & are without tubercles on front. Takahashi (1933),Jiang et al. (2012),Aoki & Kurosu (2010)
Only species, Doraphis populi, feeds on poplar (Populus, Salicaceae). Immature alatae form groups on the undersides of leaves. Some populations anholocyclic, with two parthenogenetic generations per year.
Apterae rather large, aleyrodiform, dark, flattened, almost circular, secretes wax from ring of marginal glands. Alatae purplish brown, usually with 4-segmented antennae. Unbranched media on fore wings, and single oblique vein in hind wings. Close to Cerataphis, but differs in wing venation. Takahashi (1930),Blackman & Eastop (1982-)
Most species host alternate between a gall stage on witch hazel (Hamamelis, Hamamelidaceae) and a pseudogall on birch (Betula, Betulaceae). Others remain anholocyclically all year on birch. May vary geographically within species. The life cycle of host alternating species takes two years with the sexual stage on witch hazel.
Apterae rather small, wax-covered aphids living in a gall or pseudogall on the under or upper side of the leaf. Antennae very short, 3- or 4-segmented. Legs rather short and thick; tarsi are wanting on first
and second pairs. Without siphunculi. Cauda prominent and knobbed. Anal plate small, bilobed. May get separate aestivating & hibernating forms. Alatae have two oblique veins in the hind wing, and siphuncular pores. Theobald (1929)
One species with gall stage on witch hazel (Hamamelis, Hamamelidaceae) alternating to birch (Betula, Betulaceae), one species monoecious holocyclic on witch hazel, one species varies geographically.
Secondary host apterae are inconspicuous aleurodiform with a fringe of radiating wax filaments. Antennal tubercles undeveloped, and front of head convex. Eyes triommatidia. Antennae reduced to small inconspicuous papillae, with 1 or 2 segments, without rhinaria.
Alatae of nearctic species have 3-segmented antennae, 5-segmented in those morphs in the palaearctic species. Numerous annular secondary rhinaria present on segment III. Terminal process absent. Compound eyes present. Fore wings of alate have reduced venation, with an unbranched media vein and branches of cubitus arising from short common stem. Siphunculi absent, cauda knobbed. Anal plate is bilobate. Blackman et al. (2019)
Only species, Protohormaphis piceae, feeds on needles of blue spruce (Picea pungens, Pinaceae).
Apterae small, oval, slightly flattened, dark green. Immatures are lighter bluish green with white wax markings. Antenna 4- or 5-segmented. Dorsum entirely sclerotised, with head and prothorax fused. Cauda knobbed. Blackman & Eastop (1982-)
Tsugaphis sorini feeds on southern Japanese hemlock (Tsuga sieboldii) or spruce (Picea) (both Pinaceae). One species lives in yellow depressions on needles, which eventually become twisted & brittle, and drop prematurely. Only apterous viviparae known.
Apterae are very small, body depressed & flattened, pale green, darkening with age. Without wax pores. Head and thoracic segments fused, and abdominal segments fused. Head without frontal tubercles. Eyes triommatidia. Antennae short, 4-segmented, without secondary rhinaria. Legs short, concealed under body. First tarsal segments with 2 or 3 hairs. No siphunculi. Cauda constricted basally & globular. Takahashi (1957)
Only species, Allothoracaphis piyananensis feeds on undersides of leaves along main veins of Quercus glauca & Quercus morii (both Fagaceae). Apparently anholocyclic.
Body ovate, depressed, flattened, not strongly sclerotized, with long marginal hairs on prosoma. Abdomen much reduced in size, separated from, but sunken into cephalothorax, the anterior part (tergites I-VII) without submarginal hairs. Eyes triommatidia. Antennae small, ventral, longer than wide, 3-segmented. Legs very short, concealed under body; tarsi
well developed, 2-segmented, with well developed claws. Dorsum with irregular mosaic-like structures, minutely dentate
at margin. Tergite VIII with 4 hairs. Siphunculi absent. Cauda broader than long, constricted basally. Anal plate deeply bilobed. Related to Thoracaphis, but differs in absence of siphunculi & presence of mosaic-like structures on the dorsum. Alate morph unknown. Takahashi (1958)
Primary host of Asiphonipponaphis vasigalla is isu tree (Distylium racemosum var. chinense, Hamamelidaceae), secondary host unknown. Produces unique gall on Distylium, vase-shaped, green, with flower-shaped opening at the tip through which large honeydew droplets coated with white wax drip.
Apterae on secondary host unknown. Emigrant alatae with 5-segmented antennae; annular secondary rhinaria on segments III-V. Rostrum short. First tarsal chaetotaxy 3,3,3. Forewings with long, narrow pterostigma; media unbranched, not united with cubital, two cubital veins fused at base; hind wings with 2 obliques. Siphunculi absent in both fundatrix & alatae. Cauda knobbed, distinctly constricted at base. Chen et al. (2011)
Four species live on (presumed) secondary host, oak, especially Japanese blue oak (Quercus glauca, Fagaceae). One species lives on (presumed) ancestral primary host winter-hazel (Distylium).
Apterae on secondary host have body ovate, convex, not depressed, strongly sclerotized. 20 marginal hairs around cephalothorax, 6 of which are between eyes. Eyes marginal, with 3 facets. Antennae ventral, longer than wide, 3-segmented. Legs very short, hind legs more or less concealed; tarsi rudimentary, not segmented. Abdomen much reduced in size, separated from cephalothorax, without hairs on anterior part; tergite VIII with 4 hairs. Dorsum with irregular mosaic-like structures, which are protuberant and rounded apically. Siphunculi absent. Cauda broader than long, constricted basally. Anal plate deeply bilobed. Takahashi (1958)
Only species, Distylaphis foliorum, produces spherical green-reddish-brown galls on the leaves of winter hazel (Distylium stellare, Hamamelidaceae). Also free-living generations on undersides of leaves of same host. Classed as monoecious holocyclic, but further studies may reveal secondary host. First instar soldiers present.
Emigrant alatae rather large, long forewings, with broad black pterostigma, basal area of forewing & cubital vein brown. Annular secondary rhinaria on antennal segments III-V. Apterae rather small, greenish, margins of body thickly powdered in wax, dorsum with transverse wax patches. Antennae 4-segmented. Eyes triommatidia. Apical rostral segment 0.76-0.82 x second hind tarsal segment. First tarsal segments have 3,3,2 hairs. Circular wax glands present on head, thoracic & abdominal segments, Siphuncular pores on segment VI. Cauda with 2 hairs. Noordam (1991)
Euthoracaphis4 spp. India to Japan to Java, 1 now in California
Most Euthoracaphis feed on members of laurel family (Lauraceae), especially cinnamon (Cinnamomum), Sassafras variifolium and California bay (Umbellularia californica). Euthoracaphis umbellulariae anholocyclic in California, but life cycles of most species unknown.
Apterae are flat, oval, scale-like, wax-covered. Prosoma divided by sutures into one large median & two lateral areas. Antennae in apterae short, 3-segmented. Rostrum short and stout. Number of hairs on first tarsal segment is 3,3,2 or 3,3,3. Abdominal segments II-VII fused, and distinctly separated from prosoma and abdominal segment VIII. Dorsum of aptera has scattered sculpture or pustules. Dorsal hairs long, fine, either sparse or numerous. Abdominal tergite VIII has 2 or 4 hairs. Siphunculi small and pore-like. Cauda constricted at base, distinctly knobbed, with a few hairs. Anal plate bilobed. Alatae have 5-segmented antennae, with annular secondary rhinaria. Fore wings have pterostigma a little dusky, with vein sometimes distinctly bordered brownish. Chen et al. (2009)
Hybothoracaphis laevigata feeds along veins on undersides of leaves of Quercus aquifolioides (Fagaceae).
Apterae are rather small, dark brown, aleyrodiform, strongly sclerotized, with a conspicuous median dorsal ridge. Prosoma consisting of fused head, thorax, and abdominal segment I; abdominal segments II-VII fused and
separate from prosoma and abdominal segment VIII. Dorsum of prosoma nearly smooth, with clusters of irregular-shaped pustules along central axis and a wide transversely striped band marginally. Submarginal hairs on prosoma and abdominal segments II-VII. Eyes triommatidia. Antennae small, unsegmented. Rostrum short. Legs short, exposed outside body. First tarsal chaetotaxy: 2-3,3,2. Siphunculi pore-like. Cauda knobbed, constricted at base. Chen et al. (2016)
Indonipponaphis fulvicola produces almost globular galls in cusps of young leaves on isu tree (Distylium racemosum, Hamamelidaceae). Alate emigrants migrate to secondary hosts, oak (Quercus spp, Fagaceae), especially Q. acuta, Q. gilva, Q. dealbata. Primary host of I. tuberculata unknown.
Apterae on secondary host have semi-oval body. Antennae 3-segmented. Eyes triommatidia. First tarsal segments with 3,3,2 hairs. Prosoma densely covered with semioval pustules which are conspicuously protruberant on lateral margins. Thick finger-like paired spinal and marginal tubercles on prosoma and abdominal plate. Without spinal hairs on abdominal tergite VII, but pair of small tubercles present near hind end. Siphunculi pore-like. Cauda semi-oval, constricted at base. Close to Nipponaphis, but differs in having finger-like tubercles on prosoma and abdomen. Ghosh et al. (1983)
Mesothoracaphis rappardi feeds on young shoots or older twigs of Dendrophthoe pentandra (Loranthaceae), Viscum articulatum (Viscaceae).
Apterae of Mesothoracaphis rappardi rather small, brownish-black, somewhat shiny. Has sclerotised, box-like body and greatly reduced antennae and legs. Body comprises prosoma, fused tergites II-VII, & dorsally free tergite VIII. Wax gland groups lacking. Head without horns or dagger hairs. Antennae 3-segmented, less than 0.1 x body length. Eyes triommatidia. Legs strongly sclerotized, reduced. Siphunculi with small pore. Cauda transversely elongate, knobbed with constriction. Anal plate strongly bilobed. Noordam (1991)
Two species host alternate between winter-hazel (Distylium, Hamamelidaceae) and chinquapins (Castanopsis, Fagaceae), most other species only known from Fagaceae.
Apterae on secondary host are rather small to medium-sized, circular to oval, flattened, strongly sclerotized, dark brown or black. Antennae short, nearly reaching eyes, appearing to be 2-segmented. Rostrum short. Prosoma not well defined from anterior fused part of abdomen. Ornamentation of tergum characteristic, consisting of rounded pustules which are rather evenly spaced and sized over the central part of the prosoma and which, under the light microscope, appear double-walled or ring-like. Dorsal hairs of prosoma very short, pointed. Fused abdominal tergites II-VII have marginal hairs but there are no spinal hairs on abdominal tergite VII, and abdominal tergite VIII usually has 2 hairs. Cauda pale, constricted at base, much broader than long, with about 8 hairs. Anal plate pale, with 5 long hairs on each lobe. Takahashi 1959,Blackman & Eastop (1982-)
Metathoracaphis isensis produces yellowish green, semicircular or helmet-shaped galls on isu tree (Distylium racemosum, Hamamelidaceae). Secondary host is red-bark oak (Quercus gilva, Fagaceae). Dioecious holocyclic, but some populations anholocyclic.
Apterae on secondary host are aleyrodiform, oval, somewhat convex dorsally, strongly sclerotised, blackish brown dusted with greyish wax. Prosoma with faintly circular structure on submarginal area and minute marginal wax pores. Eyes triommatidia. Antennae very short, not segmented. Tarsi well developed. First tarsal segments with 3,3,2 hairs. Abdominal tergites II-VII fused with prosoma anteriorly, but with distinct traces of division, with 6 short hairs on each side. Tergite VIII separated with 2 hairs. Siphunculi absent. Cauda broader than long, constricted basally. Alatae with 5-segmented antennae, also without siphunculi. Sorin (1987)
Both Neodermaphis species feed on twigs of Japanese blue oak (Quercus glauca, Fagaceae).
Apterae black with white wax powder on side. Body very small, ovate, flattened on dorsum, strongly sclerotized. Eyes triommatidia, with 1 facet isolated from other 2 facets. Antennae reduced, very small, faintly 2-segmented. Legs stout, tarsi reduced with small claws. Dorsum of prosoma with 4 pairs of indistinct rather large circular pale parts when cleared with potash. Closely related to Dermaphis, but differs in small body size, much reduced antennae, and eyes not being protruberant. Alatae undescribed. Sorin (2006)
Neohormaphis calva produces pale greenish, semiglobose, downy galls on upper sides of leaves of winter-hazel (Distylium stellare, Hamamelidaceae). Immature alate secrete unusual glassy wax filaments from large circular dorsal wax glands. Secondary host oak (Quercus, Fagaceae).
Emigrant alatae medium-sized, black head & thorax, grey abdomen. Head smooth without horns or dagger hairs. Antennae 5-segmented with ring-shaped secondary rhinaria on segments III-V. Wing venation unusual, the media, Cu1a and Cu1b all arising from common stem. Siphunculi on segment VI, without hairs. Cauda hardly developed, transversely elongate with 4-6 hairs. Apterae on secondary host with prosoma consisting of head, thorax & abdominal segments I-VII dorsally fused, segment VIII free. Distinct transverse furrow between muscle plates between pro- and mesonotum. Noordam (1991)
Only known from secondary host, chinquapins (Castanopsis, Fagaceae), where apterae live on branches, are ant-attended & largely wax-free. Primary hosts most likely winter-hazel (Distylium, Hamamelidaceae), where probably produce galls.
Apterae on secondary host aleyrodiform, flattened dorsoventrally, without frontal horns, and strongly sclerotized. They comprise three parts: the prosoma; abdominal segments II-VII fused together, but distinctly separated from prosoma; abdominal segment VIII. Strongly sclerotised prosoma bears pustulate ornamentation and numerous fine hairs. Eyes triommatidia. Antennae much reduced, indistinctly 3-segmented, with primary rhinaria placed wide apart. Rostrum short and thick. Each tergite has pair of rather long submarginal hairs, with 4-8 hairs on tergite VIII. Tergites II and VII each have a pair of spinal hairs. First tarsal segments have 2,2,2 hairs. Siphunculi in apterae small & pore-like. The cauda is knobbed and constricted at the base. Similar to Nipponaphis, but that does not have fused abdominal segments distinctly separated from the prosoma, and does not have numerous fine hairs on the prosoma. Chen & Qiao (2012),Takahashi (1962)
Only species Neoreticulaphis nipponica feeds on uppersides of leaves along mid-ribs of red-bark oak (Quercus gilva, Fagaceae). Anholocyclic with one generation per year. Alatae unknown.
Aptera very small, blackish brown to black, almost circular with dorsum somewhat domed, strongly sclerotized. Prosoma large, with reticulation of minute circular pores over most of surface; 18 minute circular pores arranged on submarginal part in single row. Eyes small on protuberances. Antennae very short, faintly 2-segmented, concealed under body. Legs also concealed under body. Fore-tarsi without claws. Abdomen very small, wider than long. Siphunculi absent. Cauda slightly constricted basally, knobbed part wider than long. Sorin (1999)
Host alternation and gall formation on winter-hazel (Distylium, Hamamelidaceae) only established for one species (N. yanonis). Several species ? anholocyclic on evergreen oak (Quercus), with apterous vivipara only known morph.
Apterae very small, body oval or elongate oval, flat, usually black with white wax & strongly sclerotised. Prosoma consists of fused head, thorax and abdominal segment I, abdominal segments II-VII fused, and abdominal segment VIII free. Dorsum of prosoma with mosaic sculptures or corrugated and lacking long hairs. Antennae in apterae unsegmented on venter of head, in alatae five-segmented, with annular secondary rhinaria. Rostrum very short, two-segmented in apterae, normal in alatae. In apterae, fore and middle legs very short, concealed under body, and without tarsi; hind legs longer, protruding behind body, with rudimentary unsegmented tarsi. First tarsal segments with 3,3,2 or 3,3,3 hairs. Siphunculi absent in apterae and porelike in alatae. Cauda knobbed and constricted at the base. Chen et al. (2011)
Some spp. host alternate between galls on winter hazel (Distylium, Hamamelidaceae) and oaks (Fagaceae). Galls may take more than a year to mature, and the complete life cycle can take 2-5 years. Other spp. apparently anholocyclic on Fagaceae, Lauraceae and Moraceae.
Apterae on secondary hosts are aleyrodiform, brown & yellowish, dark purple or black, with furrows and wrinkles; sometimes covered with thin layer of wax. Body comprises prosoma, fused tergites II-VII, & tergite VIII free, with prosoma much the longest part. Prosoma is densely covered in pustules, varying in size & shape between species. Antennae with 3 or 4 segments, bent sideways on segments I & II. Eyes triommatidia. Apical rostral segment up to about twice second hind tarsal segment. Hairs on dorsum of prosoma & abdomen rather sparse. Siphunculi poriform. Cauda with knob & constriction, tranversely elongate. Alatae have smoky wings. Noordam (1991)
Only species, Paranipponaphis takaoensis, feeds on branches of oak (Quercus, Fagaceae).
Apterae medium-sized, nearly circular, flattened, with venter a little expanded, "pill box-shaped", blackish-brown, not strongly sclerotized. Prosoma not distinctly defined at hind end of dorsum, with distinct mosaic-like structures or low pustules, with short dorsal hairs, but without pair of hairs close to hind end. Antennae short, 3-segmented, tapering on distal part, with 2 primary rhinaria distinctly apart from each other. Legs short, exposed; tarsi 2-segmented, with well developed claws. Anterior fused part of abdomen (tergites II-VII) with 6 submarginal hairs on each side; tergite VIII with 4 hairs. Siphunculi entirely lacking. Cauda constricted basally, much broader than long. Anal plate bilobed, each lobe much broader than long. Closely related to Nipponaphis, but differs in absence of siphuncular pores & lack of dorsal hairs close to hind end of prosoma. Takahashi (1959)
Most species in genus have oak (Quercus, Fagaceae) as (secondary ?) host, although may chang (Litsea, Lauraceae) & wax myrtle (Myrica, Myricaceae) also recorded.
Apterae have rather narrow, flattened, depressed, sclerotized body, with stout spine-like marginal hairs on dorsum. Prosoma entirely fused with abdominal plate, but tergite VIII separate, with 4 hairs. Dorsum reticulated, without papillae. Eyes triommatidia. Antennae on venter, very small, 2-4
segmented. Legs much reduced in size, concealed under body; tarsi small, but 2 segmented, with or without claws. Siphunculi absent. Cauda small, wider than long, constricted basally. Anal plate deeply bilobed. Differs from Thoracaphis in anterior part of abdomen entirely fused with the prosoma, dorsum lacking papillae, & absence of siphunculi. Takahashi (1958),Chen et al. (2016)
Pseudothoracaphis1 sp. Himachal Pradesh, Uttar Pradesh, India, N.E. Pakistan
Only species, Pseudothoracaphis himachali, feeds on oak (Quercus baloot, Q. griffithii, Q. incana, Q. oblongata, Fagaceae). Lives in ant-attended colonies on undersides of leaves
Apterae have body semioval, dorso-ventrally flattened, strongly sclerotized, dark brown. Eyes 3-faceted. Antennae 3-segmented. Prosoma and abdominal segments (II-VII) completely separated; marginal hairs on prosoma and fused abdominal segments absent; dorsal hairs minute. Dorsum of prosoma wrinkled and sculptured but without
pustules; submarginal area appears reticulated, long submarginal hairs on prosoma absent. Rostrum short. Legs normal with claws; tergite VIII with 2 spine-like hairs. Cauda knobbed. Anal plate bilobed. Similar to Allothoracaphis in the 3-segmented antennae and claws on legs and in absence of siphunculi and marginal hairs on fused abdominal segments, but differs from it in not having long marginal hairs on prosoma. Raychaudhuri et al. (1980)
Quadrartus yoshinomayai galls twigs of isu tree (Distylium racemosum, Hamamelidaceae) in spring, later migrating to oak (Quercus acutissima, Fagaceae). Galls on Distylium closed, pouch-like, covered with wart-like protuberances. Heteroecious holocyclic with 2 (or more) year life cycle. Quadrartus agrifoliae anholocyclic on evergreen oak (Quercus phylliraeoides, Fagaceae).
Apterae on secondary host very small, dark brown or yellowish-brown, sometimes secreting greyish needle-like wax. Body strongly sclerotized, dorsum flattened. Antennae and tarsi both greatly reduced, antennae 4-segmented. Dorsal cuticle subdivided into ornamented plates. Venter with lateral outgrowths. Emigrant alatae with 4-segmented antennae, secondary rhinaria on segments III & IV, hyaline wings, and a yellowish green abdomen. Siphunculi present as elevated small pores. Cauda small, spherical and strongly constricted at base. Monzen (1954),Sorin (2001)
Type species of genus, Quernaphis tuberculata, was formerly regarded as anholocyclic on the secondary host, oak (Quercus, Fagaceae). Now clear that Metanipponaphis (= Monzenia) minuta, a gall-forming species on Distylium, is the primary host form of another very similar Quernaphis species, now called Quernaphis minuta. Galls have small chimney-like projection, allowing first instar soldier nymphs access to gall exterior.
Apterae on the secondary host yellow to white, with ovate body, flattened on dorsum, irregular and asymmetrical in shape, with venter irregularly expanded beyond margin of dorsum, sclerotized, with large dorsal hairs. Papillae well developed on dorsum, but absent on pleural region. Antennae short, 3-segmented. Eyes small, with 3 facets. Legs short, exposed; tarsi reduced in size, not segmented, without claws. Abdomen much smaller than prosoma, with fused tergites II-VII indistinctly defined from it, with 6 large hairs in a row along each lateral margin; tergite VIII separated, with a pair of setae. Siphunculi absent. Cauda broader than long, constricted basally, concealed under body. Alate sexuparae of type species have unbranched media in forewing and hindwing without any oblique veins. Takahashi (1958),Aoki et al. (2024)
Reticulaphis9 spp. E&SE Asia, 2 now in Europe, Australia
Most species known from secondary host forms feeding on figs (Ficus, Moraceae) or Fagaceae. Primary host known for one species to be Distylium (Hamamelidaceae). In areas where primary host is not present, populations are anholocyclic.
Apterous viviparae are ovate or elliptical, & aleyrodiform (=depressed and flattened). Antennae short, ventral, 2- or 3-segmented. Eyes submarginal, with 2 or 3 facets. Cephalothorax strongly sclerotized and reticulated, without papillae, & with 20 long hairs on marginal area, 6 between eyes. Abdomen small, separated from cephalothorax, & with 6 minute submarginal hairs on each side of the anterior part (tergites I-VII). Tergite VIII has at least one pair of hairs. Legs short, hind legs a little exposed, tarsi rudimentary, & not segmented; claws rudimentary or atrophied. Siphunculi absent. Cauda much broader than long, constricted basally. Anal plate deeply bilobed. Related to Thoracaphis but that does not have dorsum reticulated nor rudimentary tarsi, but has papillae & siphunculi. Yeh et al. (2008).
Schizoneuraphis9 spp. E&S Asia, 1 also in Australia
Most species only known from secondary hosts Litsea, Lindera, Persea or Quercus (Fagaceae), but 1 species known to host alternate between galls on winter hazel (Distylium stellare, Hamamelidaceae) & leaves of Litsea glutinosa. Life cycles mostly unknown.
Aptera on secondary host has prosoma as flat plate, with pustules along furrows & around muscle plates; fused tergites II-VII have lateral & posterior margins thickened & with crest; tergite VIII free with margins as above. Each of three parts separated by furrows. Head without horns or dagger hairs. Antennae with 3 or 4 segments, more or less fused, bent sideways on segments I & II. Eyes triommatidia. Anterior of prosoma has long basally thick hairs. First tarsal segments with 3,3,2 hairs. Siphunculi apparently on segment VI. Cauda with knob & constriction, transversely elongate. Closely related to Nipponaphis, but their apterae lack long, basally thick prosomal hairs. Noordam (1991)
Feed on Persea (= Machilus), Holboellia (both Lauraceae), or stone oak (Lithocarpus, Fagaceae). Life cycles unknown.
Apterae medium-sized, with convex body, blackish-brown, with yellowish-brown cauda. With or without wax. Antennae 4-segmented. Rostrum short. Tarsi normal with claws. Prosoma & abdominal segments II-VII fused together. Dorsum densely covered with spine-like processes. Abdominal tergite VIII with 2 long hairs. Siphunculi pore-like. Alatae with 5-segmented antennae, segment III nearly as long as IV & V together, with secondary rhinaria on segments III-V. Forewings distinctly infuscated at basal part. Ghosh & Raychaudhuri (1973)
Species described now only known from parthenogenetic generations on what were the original secondary hosts, oak (Quercus, Fagaceae) & laurel (Lindera, Cinnamomum, Lauraceae).
Thoracaphis have aleurodiform apterae. Head without horns, eyes triommatidia, with very short 3-segmented antennae. Apical rostral segment is 1.10-1.18 x the second hind tarsal segment. Prosoma completely or incompletely separated from the fused abdominal segments II-VII. The fused abdominal segments have 6 pairs of marginal hairs. Tergite VIII has 2-4 hairs. First tarsal segments have three hairs, of which middle one is stout and spiny. Siphunculi pore-like. Cauda broader than long. Anal plates bilobed. Alatae with 5-segmented antennae with annular secondary rhinaria. Forewings have media vein once branched and the hind wings have both obliques. Takahashi (1958),Noordam (1991)
Tripartita formosana produces galls on isu (Distylium racemosum), & Distyliopsis dunnii (both Hamamelidaceae). Galls green, vase-shaped, on upper sides of leaves, but openings on undersides. Several galls on single leaf. First instar sterile soldiers ? on surfaces of galls and leaves.
Alate emigrants from gall are medium to rather large. Antennae long, more than
half body length, 3-segmented; segment III often thickened on basal 1/3-1/2, with numerous annular secondary sensoria. Rostrum short, not reaching mid-coxae; rostral segments IV+V blunt. Prothorax well-developed & prominent, with 2 groups of wax glands on tergite. Tibiae imbricate, with distinct spinules. First tarsal segments with 3,3,3 hairs. Groups
of wax glands present on abdominal segments I-VII. Siphunculi absent. Cauda transverse, not constricted at base. Anal plate bilobed. Yeh & Ko (2017)
Feeds on short-lived annual grasses (Poaceae). Monoecious holocyclic with sexuales produced following autumnal rains, and diapausing eggs laid in spring before hot dry season.
Body slender, bearing 10 long fleshy imbricated tubercles; 4 on each of
segments VII and VIII and 2 larger ones on ??segment IX (described as such by Essig, 1953). Eyes compound with ocular tubercles. Antennae long and slender with small circular secondary sensoria. Rostrum short. Siphunculi greatly enlarged in the middle and constricted basally and anteriorly. Anal plate shallowly bilobed. Cauda elongate, constricted
near base. Essig (1953)
Cinara255 spp. N America + Europe to E Asia, a few now in Africa, Australia
Live on conifers (Pinaceae, Cupressaceae). Monoecious holocyclic. Feed on roots, branches, or foliage. Often attended by ants.
Apterae rather large to very large, frequently wax-powdered, densely haired. Antennae shorter than half body length. Rostrum relatively long reaching behind hind coxae; apical rostral segment slender, pointed and very long, & comprising two segments. Abdominal dorsum has 6 or more longitudinal rows of small, dark brown intersegmental muscle sclerites. Siphunculi are pore-like and located on broad, often pigmented, hairy cones. Cauda always broader than long, either rounded or triangular. Oviparae often have perianal ring of wax. Blackman et al. (2019)
Essigella17 spp. N America, 1 now in S America, Europe, Australia
All species live and feed on pine needles (Pinus) except for one species on Douglas fir (Pseudotsuga) (both Pinaceae). They are often overlooked, as they feed near the bases of the need and move quickly when disturbed. Some have now been recorded as invasive species in Europe.
Apterae medium sized, greenish, spindle-shaped, with tapered narrow abdomen, but "spindle" truncated at head end, which is relatively broad. Antennae 5-segmented. Ocular tubercle absent. Claws with modified apices, bifurcate or double. Abdominal tergites lightly to heavily sclerotized, not necessarily pigmented. Siphunculi pore-like or very short. Cauda round. Forewing of alate with radial sector straight. Similar to Eulachnus, but smaller and with 5-segmented antennae. Pike et al. (2003),Blackman et al. (2019)
Eulachnus24 spp. W Europe to E Asia, few now almost WW
All species live & feed on pine needles (Pinus, Pinaceae). Monoecious holocyclic. Cryptic when feeding, but very active when disturbed. Not usually attended by ants.
Small, narrow and elongate greenish to olive brown aphids with long limbs. Frontal tubercles undeveloped. Antennae 6-segmented, with terminal process shorter than base of last segment. Dorsal hairs placed on scleroites. Siphunculi slightly elevated, barely visible, rim-like structures, without surrounding hairs. Pike et al. (2003),Blackman et al. (2019)
Only species, Pseudessigella brachychaeta, feeds on Bhutan pine (Pinus griffithii (= wallichiana), Pinaceae). Monoecious holocyclic. Alatae unknown.
Body elongated, narrow, pale green, with few hairs. Eyes without distinct triommatidia.
Antennae rather short, in adults of 5 segments. Last rostral segment not subdivided, very short
and blunt. First tarsal joints with 5 ventral hairs, no dorsal hairs. Claws with simple, not cleft
apices. Tergum membranous, with very small scleroites around bases of dorsal hairs. Siphunculi, rimmed pores on a very small, hairless sclerite. Cauda rounded. Most closely related to Eulachnus, but Pseudessigella have 5 instead of 6 antennal segments. Differs from Essigella in having claws with simple, acute apices. Hille Ris Lambers (1966)
Mainly feed on the twigs and branches of broadleaved trees especially oaks (Quercus), chestnuts (Castanea and beeches (Fagus) (all Fagaceae). Monoecious holocyclic. Nearly always attended by ants.
Medium to large brown or black aphids. Antennae short, not more than half body length. Rostrum long so can penetrate woody tissue. Legs long, especially hind legs which have very long, often curved, tibiae. Siphunculi conspicuous pores on dark hairy cones. Cauda and anal plate rounded. Wings relatively small, compared with large body; more than half area of forewings pigmented. Blackman et al. (2019)
Bark-feeding aphids which are unusually polyphagous in their choice of host
Apterae & alatae very large, brownish or black, dusted in wax. Antennal tubercles undeveloped. Antennae 6-segmented, with short terminal process and few hairs. Apterae without secondary rhinaria, but commonly present on segment III in apterous-alate intermediates, which are common; present in alatae on segments III-V. Rostrum clearly 5-segmented, but segment V fused caplike to apex of IV. Forewing in alate has long stigma, extending around the tip of the forewing. Abdominal marginal tubercles absent. Siphunculi short, almost poriform, each on large subcircular mammiform base. Cauda short, anal plate entire. Wilson (1909),Foottit & Richards (1993)
Feed at stem base or on roots of rose (Rosa), also Geranium & Potentilla (all Rosaceae). Monoecious holocyclic. Attended by ants.
Medium-sized to rather large aphids, dark brown. Antennal terminal process very short, usually less than 0.25 x base of segment. Dorsal hairs often placed on dark scleroites. Siphuncular cones low, hairy & conical. Alatae have no distinct pattern of pigmentation on forewings, but have black spot at base of pterostigma. Blackman et al. (2019)
Pterochloroides1 sp. S. Europe, N. Africa, S.W. & C. Asia.
Feed on woody Rosaceae, esp. Prunus spp. In cooler regions Pterochloroides aphids are monoecious holocyclic; in warmer countries populations are mainly anholocyclic.
Apterae of Pterochloroides persicae are very large, dark, with white wax patterning. Antennae 6-segmented, less than half as long as body, with short terminal process. There are secondary rhinaria on segments III-IV. Rostrum reaches to middle of abdomen, with apical rostral segment at most 0.80 x as long as the second segment of hind tarsus. Dorsum with double row of large pigmented spinal tubercles. Hairs on the flagellum and dorsum are thick & short. Siphuncular pores on broad dark hairy cones. Cauda dark sclerotic, with many fine hairs. Alatae have the pterostigma, areas between medial branches, and between anal and cubitus vein pigmented. Lachnus, Longistigma & Maculolachnus do not have series of dark spinal tubercles. Ghosh (1982)
Stomaphis feed on the stems and roots of a variety of tree species,
with most species on oak (Quercus, Fagaceae), birch (Betula, Betulaceae), maple (Acer, Aceraceae), and willow (Salix) & poplar (Populus) (both Salicaceae). Always ant attended.
Rather large or very large oval aphids which are characterized in the females by a very long rostrum, about twice body length. Antennae 6-segmented & densely hairy; terminal process has 20 or more hairs. Second segment of the hind tarsus rather long compared with other lachnids. Siphunculi are pores on low, haired, cones. Alatae have rather short narrow wings. Males are small, apterous and without mouthparts. Blackman et al. (2019)
Eotrama species feed on roots. Host plants are Myricaria & Tamarix (both Tamaricaceae) & possibly thistle (Cirsium, Asteraceae).
Apterae very large, pale yellowish or creamy white. Head & body clothed with numerous fine hairs. Antennae 6-segmented. Eyes compound with small triommatidium. Rostrum quite long, not much shorter than body, with subdivided last segment. Hind coxae elongate, twice as long as middle coxae. Second hind tarsal segment not much longer than those of other tarsi. Siphunculi on aptera not on pigmented cones. Forewings with obliquely truncated stigma. Differs from Sinolachnus which have coxae of all legs very similar. Hille Ris Lambers (1969)
Protrama feed on underground parts of daisies (Asteraceae), (especially thistles and wormwoods), or of buttercups (Ranunculaceae).
Apterae medium to large, creamy white to brownish green. Apterae normally alatiform, with dark dorsal cross bands & dark siphuncular cones. Eyes large with many ommatidia & ocular tubercle. Antennae about half body length. Secondary rhinaria present in alatae and alatiform apterae. Hind tarsus very long, 0.5-0.9 x hind tibia. Fore wing in alatae with indistinct media & radial sector; media with one or two forks. Siphuncular cones low and hairy. Cauda rounded. Heie (1995)
Most species of Sinolachnus feed on stems, branches & roots of oleaster (Elaeagnaceae), with one species on roots of berries (Rubus, Rosaceae). Life cycles unknown, but some apparently anholocyclic.
Apterae rather large, reddish brown or blackish. Head with membranous median suture. Antennae 6-segmented. Rostrum with subdivided, rather acute apical segment. First tarsal segments with several short & longer hairs. Body very hairy, dorsally reticulated, with small intersegmental sclerites, & sclerotic band on tergite VIII. Siphunculi pigmented cones. Alatae with exceedingly large number of strongly protruding, very small secondary rhinaria from base of segment III to just past primary rhinaria on VI. Forewings only pigmented along anterior margin. Hille Ris Lambers (1956)
Mostly living on the roots of Asteraceae where they are attended by ants. Long considered as wholly anholocyclic, but some sexual reproduction may occur.
Apterae medium to rather large, pale brown or whitish and densely hairy, with small compound eyes and no dark dorsal pigmentation. Antennae about 0.5 x body length, with antennal terminal process less than 0.25 x base antennal segment 6. Hind tarsus greatly elongated. Species in the subgenus Neotrama) have siphuncular pores on low cones, but species in nominate subgenus have neither siphunculi nor siphuncular pores. The cauda is rounded. Heie (1995)
Indolachnus himalayensis (formerly Lachnus himalayensis)
feeds on loquat (Eriobotrya dubia & E. petiolata, Rosaceae). Form large colonies on underside of leaves & petioles, apparently without injury to plant.
Apterae very large, pear-shaped, brick red, with very distinct segmentation with whitish intersegmental lines. Legs black. Body densely covered with very fine brown hairs. Antennae 6-segmented, with 1-2 secondary rhinaria on segment IV. Antennal hairs very numerous, quite long; terminal process with 1 subapical hair. Rostrum long reaching hind coxae. Abdomen membranous, with light brown siphuncular sclerites. Cauda broadly rounded. Differs from Nippolachnus in having larger size, pear-shaped body (narrow oval in Nippolachnus), and having all legs uniformly black (yellow or at most dusky in Nippolachnus). Kanturski et al. (2024)
Feed on branches & stems of plum/cherry trees (Prunus, Rosaceae). Populations are holocyclic, and fundatrices & sexuales have been described. Ant attended.
Apterae medium-sized, pear-shaped, blackish with prominent white wax marks on the dorsum. The dorsum is densely covered with numerous long, fine, pointed hairs, and with clearly visible denticles. Frons with distinct epicranial suture. Antennae 6-segmented with secondary rhinaria on ANT III-IV. Arrangement of accessory rhinaria on the last antennal segment is unique. They are divided into two groups: a single situated separately over primary rhinarium on the terminal process, remaining accessory rhinaria tightly adhere to each other next to the primary rhinarium. Antennal segment III shorter than IV + V+VI. Legs densely covered with numerous, quite long & pointed hairs. First tarsal segments of the fore and middle legs have large numbers of peg-like hairs. Tergite VIII has a dorsal cross-band. Siphunculi on large cones with denticles and a poorly developed flange; densely covered with hairs. Cauda circular or semi-circular, with 20-25 long, pointed hairs. Kanturski & Lee (2024)
Live on woody Rosaceae, mainly loquat (Eriobotrya) & pear (Pyrus). All morphs feed on the leaves of their host plants, never on woody parts
Apterae are oval, pale green or completely pale without visible sclerotisation, and very densely covered with long, fine, pointed, unpigmented hairs. Genus characterised by absence of ocular tubercle, with the residual triommatidium located under the compound eyes. Antennae six-segmented, sometimes with one small secondary rhinarium on segments III & IV. Apical rostral segment wider at proximal part, with distal part with blunt, button-shaped last segment (RV). Siphunculi on low, delicate, and unpigmented and hardly visible sclerites with rather large rounded pores. Cauda rounded. Alate viviparous females are characterised by characteristic patterns of sclerotisation on the abdomen and membranous parts covered in
wax. Kanturski et al. (2024)
Feed on stems & branches of woody Rosaceae especially Prunus. Believed to be holocyclic in China, where spring and autumn migrations have been observed. Apparently anholocyclic elsewhere.
Apterae rather large to very large, brown or yellowish. Body clothed with numerous hairs, which are considerably longer than basal diameter of antennal segment III. Antennae six segmented, hairy, usually with few secondary rhinaria. Eyes with distinct triommatidia. Rostrum with subdivided, rather blunt last segment. Abdominal dorsum pale with intersegmental sclerites, occasionally with great many scleroites. Siphunculi on dark sclerotic cones. Cauda semioval, dark sclerotic. Alatae have pterostigma much longer than its maximum width, not reaching tip of wing. Basu & Hille Ris Lambers (1968),Ghosh (1982)
Tuberolachnus3 spp. China, India, Indonesia + 1 orig. E Asia? now virt. WW
Tuberolachnus (Tuberolachnus) salignus feeds on willows (Salicaceae). Appears to be anholocyclic as no sexuales ever found. Sometimes ant attended. Two species in subgenus Tuberolachniella feed on loquat (Eriobotrya, Rosaceae).
Rather large aphids, grey to brown to black, one species with rows of black spots. Dorsal head sutures well defined. Frontal tubercles undeveloped. Antennae 6-segmented, about half body length, with terminal process less than base segment VI. Antennal segments III-IV with circular secondary rhinaria, primary & secondary rhinaria unciliated. First tarsal segments with numerous ventral hairs. Abdominal tergite IV bears single large dorsospinal conical tubercle, just in front of siphunculi. Siphunculi poriform on large dark hairy cones. Cauda arc-shaped. Anal plate entire. Forewing of alate has media twice-branched. Pike et al. (2003)
One species known to feed on beard heath (Leucopogon) and peach heath (Lissanthe strigosa) (both Epacridaceae). Host of other species unknown.
Apterae of one species rather small, dark reddish brown with long thick strands of white wax dorsally and laterally. Wax plates, each with associated hair, covering most of dorsum of apterae. Eyes 3 faceted. Antennae 5-segmented. Rostral segments IV and V distinct. First tarsal segments normally with 5,5,5 hairs. Spiracles reduced or entirely absent
on abdominal segment I, present in rudimentary form on segment VIII. Siphunculi
small, mammiform; each with single hair near base. Cauda constricted to form a knob with hairs. Anal plate divided into 2 lobes. In alatae antennae 6-segmented, primary rhinaria ciliated. Eyes compound with ventrally placed triommatidia. Carver & Martyn (1965)
Recorded hosts include Terminalia (Combretaceae), Nectandra & Ocotea (Lauraceae), & Bouganvillea (Nyctaginaceae). Sexuales observed for several species, so most likely monoecious holocyclic.
Apterae medium-sized, variously coloured whitish, green or brown, often covered with powdery wax. Frons without antennal tubercles. Apterae with only triommatidia. Antennal hairs short & spinelike. Terminal process very short, about 0.5 x base of segment. Dorsum with numerous hair-bearing processes on dorsum. Siphunculi truncate, reduced to mere rings. Alatae with normal eyes and ocular tubercles, and primary & secondary rhinaria on antennae. Wing venation prominent, forewing with prolonged pterostigma & straight radial sector. Media once branched. Related to African genus Paoliella.Blanchard (1923)
Paoliella28 spp. Africa, 1 in India, 2 in Guatemala
Recorded hosts include Commiphora in the Burseraceae and Combretum, Pteleopsis, &Terminalia in the Combretaceae. Life cycles mostly unknown.
Apterae are very small to rather small, variably coloured from very dark to brick red to yellowish. Apterae and often alatae have conspicuous long thick backwardly directed processes. Head with two large projecting g spines in front. Eyes are triommatidia. Antennae 6-segmented, segment III the longest, slightly longer than VI. terminal process nearly as long as base of segment. Rostrum long. Theobald (1928)
Most species of Macropodaphis feed on Potentilla (Rosaceae), but Artemisia (Asteraceae) and Carex (Cupressaceae) also recorded.
Apterae medium-sized, body oval, mostly green or lilac coloured. Ocular tubercles lie under middle of eyes. Antennae 6-segmented, with the terminal process distinctly longer than base of segment VI. Primary rhinarium on antennal segment VI with two accessory rhinaria, one basal the other distal. Antennal segment III with ciliated secondary rhinaria in apterae. Fore femora greatly enlarged, adapted to leaping. Dorsal body usually with 6 lines of dorsal tubercles; apex of dorsal tubercles with glands. Siphunculi truncated. Cauda long tongue-shaped. Anal plate slightly divided into two. Qiao & Zhang (2003)
Feed on the growing tips and young cones of spruces (Picea) or firs (Abies, Keteleeria) (Pinaceae). They have a sexual stage in the life cycle, but there is no host alternation; aphids not attended by ants.
Apterae have fused head & pronotum & well well-developed wax glands which produce covering of wax wool. Antennae short. Eyes usually 3-faceted. Siphunculi pore-like. Cauda is very small, crescent-shaped. Winged forms have forewings with elongate pterostigma, tapering to point at wing apex, and bluntly triangular cauda. Oviparae and males wingless, reduced in size. Blackman et al. (2019)
Neophyllaphis18 spp. S Hemisphere, + esp. cool parts elsewhere
Neophyllaphis are monoecious on podocarps (Podocarpaceae) and araucarians (Araucariaceae). Sexual morphs are known in some species. Generally occur in mixed colonies with parthenogenetic morphs, often over several generations through the year.
Apterae are wax secreting. Head & pronotum more-or-less fused. Antennal tubercles undeveloped. Antennae 6-segmented, with semi-annular secondary rhinaria. Primary rhinarium has hairy fringe. Eyes of apterae are triommatidia. In alate fore-wings have media twice branched; hind-wings have both media and cubitus present. Siphunculi very small & much wider than long. Cauda somewhat elongate and knobbed. Anal plate slightly divided. Oviparous females may be winged, & possess semi-annular secondary rhinaria. Cottier (1953)
Phloeomyzus1 sp. Europe, N. Africa, Asia, USA, S. America
Only species, Phloeomyzus passerinii, lives on bark and in crevices on trunks of poplar trees (Populus, Salicaceae) spp. No host alternation, only alatae are sexuales, but apterous viviparae often overwinter anholocyclically. After mating the oviparae each lay just two eggs.
Phloeomyzinae passerinii apterae are rather small to moderate sized, green, covered with dirty white wax wool. Parthenogenetic forms all apterous, with fused head & prothorax and triommatidia. Antennae 6-segmented, with terminal process shorter than segment base. Secondary rhinaria absent from all morphs. Wax glands form large faceted plates on abdominal segment VII. Siphunculi slightly elevated pores. Cauda semicircular. Anal plate entire. Wings of sexual alatae held flat at rest. Radial sector leaves from the apical part of the pterostigma. Blackman et al. (2019)
Diphyllaphis5 spp. Japan & Korea, Europe, N America
Feed on leaves of oak (Quercus, Fagaceae). Leaves may curl up and be bound together by wax secreted by aphid. Some species causing yellowing and necrosis of leaves. Most likely monoecious holocyclic.
Apterae rather small, reddish, yellowish or greenish, but appearing white under flocculent wax.
Antennae short, 6-segmented, with wax pores on basal 2 segments. Apical segment of rostrum stiletto-shaped. Legs short, tarsi with 2 hairs on first segment; empodial hairs stout & rounded at tip, or flattened and slender. Siphunculi minute, without encircling hairs, as large as dorsal wax pores. Wax pores with minute pits arranged in ring or scattered. Closely related to Stegophylla of North America, but it differs from that genus by minute siphunculi not surrounded by hairs. Takahashi (1960)
Feed on undersides of leaves of laurels (Machilus, Neolitsea, Phoebe, Lauraceae). Also recorded from Cinnamomum camphora.
Apterae medium-sized, pear shaped, pale green or yellowish (based on 1 species), covered with flocculent wax. Antennae 6-segmented, shorter than body. Secondary rhinaria present on segment III in alatae only. Apical rostral segment distinctly sclerotized at very base. Legs long, trochanters mostly distinct from femora. Tarsi with 5 hairs on first segment. Empodial hairs long & fine. Abdomen with large marginal & 4 dorsal sclerites in row on each of anterior 6 segments. Siphunculi mere rings, not surrounded by hairs. Cauda short and rounded in aptera, constricted & wider than long in alate. Resembles Phyllaphis and Diphyllaphis but differs in form of empodial hairs and structure of last rostral segment. Takahashi (1960) For live pictures see here.
Feed on the leaves of beech (Fagus: Fagaceae). They have a sexual stage in the life cycle, but do not host alternate and are not attended by ants.
Medium sized elongate oval, pale yellowish green aphids, covered with wax wool. Antennae shorter than body, with very short terminal process, less than one quarter base of last antennal segment. Rostrum rather short, not reaching middle coxae. All dorsal hairs surrounded by variably sized and variably pigmented wax gland fields. Siphunculi pore-like. Winged forms have abdomen wax-covered, with variably-developed dark dorsal cross-bars. Stroyan (1977)
All species monoecious on North American species of oak (Quercus, Fagaceae). Most likely all holocyclic, although anholocyclic populations are present.
All viviparae apterous. Eyes small, with ocular tubercle with triommatidium below, and more-or-less distinct upper half without facets. Antennae 5-6 segmented, with segment II longer than I, and often subequal to III. The first tarsal segments are always with 2 hairs. Empodial hairs very narrowly linear and blunt. Wax plates in viviparae not bordered, but groups of pores more or less bordered. Oviparae have sharply bordered subsiphuncular wax plates with facets. Siphunculi present as elevated pores, with 5-8 hairs around them. Cauda hardly visible, with hairs very much shorter than other dorsal hairs. Related to Diphyllaphis, but they have at most 1 or 2 hairs near siphunculi. Hille Ris Lambers (1966),Quednau (2010)
Live on undersides of leaves and sometimes on flowers of Humularia, also on growing tips of Aeschynomene (both Fabaceae). Monoecious holocyclic
Apterae medium-sized, slender elongate, green or yellow, without wax except in ovipara. Secondary rhinaria on antennal segments III-V. Vertex with posterior hairs in groups. On abdomen paramedian hairs in row of 6-10 on tergites I-V. In apterae & nymphs spinal and marginal body hairs are not accompanied by a small wax gland disc. Siphunculi smooth, obliquely truncate without flange. Cauda with elongate knob. Closely related to Pterasthenia but differ in lack of wax glands, and arrangement of hairs on vertex. Quednau (2010)
Mainly associated with woody Fabaceae, specifically creeping indigo (Indigofera spicata) & jixueteng (Milletia eetveldiana). Live on undersides of leaves in dry season, but in wet season found on young shoots at base of stem. Life cycle unknown.
Apterae medium-sized, slender elongate, green or yellow, either conspicuously wax-powdered or body studded with clumps of white wax. Secondary rhinaria only on antennal segment III for both apterae and alatae. Vertex with posterior hairs developed as 1 pair. On abdomen paramedian hairs developed as single spinal, pleural & marginal pairs on tergites I-V. In apterae spinal and marginal body hairs each accompanied by small cribriform wax gland disc. Siphunculi smooth, obliquely truncate without flange. Cauda with elongate knob. Stroyan (1952),Quednau (2010)
Only species, Neosensoriaphis parva feeds on Patagonian oak (Nothofagus obliqua, Nothofagaceae). Biology unknown.
Apterae rather small, with broad oval, depressed body; probably dark & wax-covered. Frontal tubercles undeveloped. Antennae of 5 or 6 segments, with 6 accessory sensoria packed against ciliated primary rhinarium; antennal segment III on aptera without secondary rhinaria. Legs rather short. First tarsal segments with 7 ventral hairs. Empodial hairs very narrowly ribbon-shaped. Dorsum of body with spinopleural sclerites developed as transverse bars and marginal sclerites. Strong pattern of polygonal reticulation of the dorsal cuticle resulting from wax gland bearing cells. Dorsal body setae short & blunt. Finger-like processes only on tergites VII and VIII, each bearing a single apical hair. Siphunculi on marginal sclerite of tergite V, short conical with almost no flange, transversely reticulated, with 1-2 hairs near base. Cauda strongly constricted. Related to Neuquenaphis, but aptera has finger-like processes only on abdominal tergites VII and VIII. Quednau (1990)
Live & feed on undersides of leaves of southern beech (Nothofagus, Nothofagaceae).
Apterae have antennae 6-segmented, segment III nearly always longer than IV, terminal process mostly very much longer than base of segment VI. Secondary rhinaria absent in aptera; present on segments III-V in alata. Rostrum reaching middle coxae, with apical rostral segment always blunt. First tarsal segments usually with 7 hairs; empodial hairs rod-shaped with slightly spatulate tip. Marginal processes always present on all tergites, horn-like or finger-like; sometimes pleural processes also present. Siphunculi usually pigmented, truncated conical. Base of cauda heavily sclerotized at edges, apex variably sclerotized. Anal plate bilobed. Alatae generally have fewer, less conspicuous processes. Quednau & Remaudiere (1994),Quednau (2010)
Feed on variety of trees, but mainly on myrtles (Myrtaceae)
Medium-sized, some species only known from alatae. Eyes of early instars only triommatidia. On aptera & alatoid nymphs usually large compound eyes develop. Apical rostral segment with only primary hairs. Empodial hairs broadly flabellate. Stigmatic plates of mesonotum with scaly sculpturing. First tarsal segments with 5 hairs. In alatae fore femora normal. Sensoriaphis & Taiwanaphis are now recognised as subgenera.
In Sensoriaphis antennal segment III is not much widened & wing veins are clear cut or with only narrow bordering. In Taiwanaphis antennal segment III often greatly swollen, and wing veins more or less thickly bordered. Takahashi (1934)
Tamalia are monoecious holocyclic on manzanitas (Arctostaphylos, Ericaceae). Live concealed in galls on leaves. Both ovipara & male are alate. Ovipara lays unusually large number of eggs.
Antennal tubercles & median frontal tubercle absent. Antennae 6-segmented, with transverse rows of minute spicules. In alatae narrow transverse secondary rhinaria. Terminal process short, less than half base of antennal segment VI. In alate forewing has the media vein twice branched. First tarsal segment has 2 dorsal and 7 ventral hairs. Siphunculi are essentially poriform. Cauda rounded, broader than long. Anal plate entire. Hottes & Frison (1931),Pike et al. (2003)
Feed on alder (Alnus) or birch (Betula) (both Betulaceae). The 3 palaearctic species feed on aerial shoots, whereas 2 North American species apparently feed underground. Monoecious holocyclic, but some with abbreviated life cycles. Usually attended by ants.
Rather small aphids, usually dark green, reddish or blackish, with conspicuous white wax spots. Eyes triommatidia. Antennae very short, hairy. Apical rostral segment tapers to thin, dark, needle-like apex. First tarsal segments with 5 hairs. Dorsum pigmented sclerotic, usually greenish or blackish, with warts & wrinkles, & many stiff, bristle-like hairs. Siphunculi present as pores on small cones. Cauda semicircular. Blackman 2019
Aphids can often be found feeding in the folded leaflets of walnut (Juglans, Pterocarya, Juglandaceae) or oak (Quercus, Fagaceae), although hosts of several species uncertain. Biology unknown.
Apterae medium-sized, greenish or yellow. Dorsum faintly sclerotized, never pigmented,
with long fine flagellate hairs. Legs with numerous spinules in rows, fore or middle, or both, tibiae with few small protuberant sensoria. Siphunculi on hairy cones. Alatae with secondary rhinaria transversely elliptical or oval. Abdomen of alate with small or rudimentary marginal sclerites, without intersegmental sclerites. Closely related to Glyphina, but Kurisakia lacks spine-like hairs & has little sclerotization of dorsum. Takahashi (1960)
Feed on Virginia creepers (Parthenocissus, Vitaceae).
In aptera head and pronotum fused, but fusion indistinct. Antennal tubercle undeveloped. Compound eye present in alata, in aptera consisting of a few facets or absent. Antennae of five segments, terminal process shorter than base segment V; primary rhinaria with ciliate margin; secondary rhinaria absent in aptera, present on segments III and IV of alata. Apical rostral segment obtuse. Dorsal body hairs almost spinelike in aptera, except those surrounding siphunculi. Hairs arranged in single pairs or transverse rows. Siphunculi almost poriform, on tergite VI, surrounded by hairs. Tergite VIII with pair of minute toothlike spinal projections on posterior margin. Cauda knobbed. Differ from Thelaxes re arrangement dorsal body hairs, and shape of apical rostral segment. Chakrabarti & Quednau (1996)
Feed on the young shoots, leaves and young acorns of various oak species (Quercus: Fagaceae). Monoecious holocyclic. Usually attended by ants.
Wingless viviparae are rather small, oval and brown or greenish, sometimes with a paler stripe along the back. The rostrum is distinctive in having a long and almost needle-like apical rostral segment. Dorsum is pigmented sclerotic, with thick spine-like hairs. Siphunculi present as pores on small cones. Cauda is distinctly knobbed. Differ from Glyphina re apical rostral segment & cauda. Blackman (2019)
Developing fundatrices induce ring-shaped galls on upper leaf surfaces of oak (Quercus, Fagaceae). Galls yellow, yellowish green or red. Fundatrices then produce sexuales, so only 2 generations a year.
Adult fundatrices are dirty green or yellow; one species with black dots on dorsum. Characterized by curious star-like dorsal tubercles with 4-11 secondary projections borne by immature fundatrices. Adult fundatrices bear small spiculose tubercles on head, thorax and abdomen. Blackman & Eastop (1982-)
Aphanostigma feed on pear (Pyrus, Rosaceae). Holocyclic in Europe with eggs laid in bark crevices. Anholocyclic populations in e.g. Israel. Attacking and sometimes destroying the buds of pear, sometimes causing necrosis around the calyx of the fruit
Very small aphids, both species yellow. Differs from Phylloxera in absence of spiracles from abdominal segments II-V. Blackman & Eastop (1982-)
For pictures see here.
Daktulosphaira1 sp. Orig. N. American, now in Europe, Middle East, Africa, Korea, China, Australia, New Zealand, C. & S. America
Only species, Daktulosphaira vitifoliae lives in leaf & root galls of grapevine (Vitis, Vitaceae). Fundatrix lays eggs parthenogenetically in the leaf gall. The offspring produce 3-4 asexual generations of grape phylloxera, Some of apterae move to feeding on roots where produce root galls
Daktulosphaira lacks prominent tuberculate dorsal and marginal processes. Primary rhinarium on antennal segment III of Daktulosphaira is not greatly enlarged as it is in Phylloxera. Alatae have paler abdominal stigmal plates than Phylloxera.Blackman & Eastop (1982)
Only species in genus, Foaiella danesii, lives on roots of Quercus robur (Fagaceae) which become tuberose. Holocyclic, producing both apterous and alate sexuparae. Overwintering eggs laid on the roots, and ? bark crevices in trunk.
Apterae very small, pear-shaped, with broad head & thorax & tapered abdomen. Apterae with fine hairs. Alatae have pale yellow head, yellow costal margin & pterostigma in the forewing. Blackman & Eastop (1982-)
Only species, Olegia ulmifoliae, produces galls on leaves of Japanese elm (Ulmus japonica). Alatae unknown. Monoecious holocyclic.
Apterae rather small, broadly pear-shaped, broadest anteriorly, without distinct head and prothorax. Possess neither wax gland nor dorsal tubercle. Antennae 3-segmented, 1 or 2 hairs on each segment, with primary rhinarium on segment III, & several hairs at apex. Rostrum short, hardly beyond middle coxae. Thorax with 2 pairs of spiracles. Tarsi one-segmented. Aoki (1973)
Phylloxera53 spp. Mainly N. America, then Europe, then Asia, a few now in Australia & NZ
Phylloxera feed on walnut (Juglandaceae) and oak/chestnut (Fagaceae). Sexual and parthenogenetic females both oviparous. Wings held flat over abdomen at rest.
Mostly rather small. Head and prothorax are fused in apterae, not in alatae. Antennal tubercles undeveloped. Eyes triommatidia in apterae, compound in alatae. Antennae 3-segmented; in aptera segment III has small preapical rhinarium; in alate have large rhinaria on III basally & apically. Rostrum 4- or 5-segmented. Prothorax without tubercles or gland facets. Apical tarsal segments have capitate hairs. Spiracles are usually small opercula, but commonly absent on the abdomen. Ovipositor rudimentary & internal. Wing venation much reduced. Foottit & Richards (1993)
Phylloxerina9 spp. N. America, Europe, Asia, 1 sp. now in Australia
Mostly species live without host alternation on willow (Salix) or poplar (Populus) (both Salicaceae), with one in galls on tupelo (Nyssa, Cornaceae). Galls caused by rolling, scalloping and swelling of edges of leaves.
Apterae yellow or pale green, usually covered in dense white wax. Head and prothorax fused in aptera. Antennal tubercles undeveloped. Eyes triommatidia. Cephalic sutures absent. Antenna 3-segmented; apical segment with subapical rhinarium having accessory sensoria in some species; secondary rhinaria absent. Rostrum 4-segmented. Hairs on head, prothorax & abdomen with clusters of gland facets around bases. Capitate hairs on apical tarsal segments. Thoracic spiracles with hinged opercula. Abdominal spiracles not evident. Siphunculi absent. Abdominal tergum VIII entire. Cauda obscure, undeveloped. Anal plate entire. No alatae ever recorded for this genus. Foottit & Richards (1993)
Our special thanks to the many photographers (credited above) and the authors who made their work available (for example under creative commons licences) or who gave us direct permission to use it. (Most of the creative commons licences are on condition of due attribution, and non-commercial use.)
We are particularly grateful to Roger Blackman and Colin Favret for their invaluable and patient assistance. In addition we must thank Shigeyuki Aoki and Masahisa Miyazaki for their kind help regarding Eumaerosiphum viciae.
We are also grateful to Colin Favret's team for Aphid species file, without which this page would have been impossible.
Aside from the references cited for individual genera above, we have drawn heavily from the following accounts:
Blackman & Eastop (1982-)
Blackman (2010 & 2019),
Heie (1980-1995),
Foottit & Richards (1993),
Quednau (1999-2010),
Hille Ris Lambers (1947 & 1949),
Hottes & Frison (1931),
Miyazaki (1971),
Noordam (1991 & 1994),
Palmer (1952),
Richards (1965 & 1971) and
Stroyan (1977 & 1984).
We fully acknowledge all these authors as the source for the (summarized) taxonomic information we have presented. Any errors in doing so are ours alone, and we would be very grateful for any corrections - or help in addressing the omissions. For assistance on the terms used for aphid morphology we suggest the figure provided by Blackman & Eastop (2006).
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