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Aphididae : Aphidinae : Macrosiphini : Acyrthosiphon : spp. list
 

 

Genus Acyrthosiphon [Macrosiphini]

Acyrthosiphon aphids are rather large broadly spindle-shaped, short-haired aphids with long antennae, legs, siphunculi and cauda. Acyrthosiphon aphids are usually green but sometimes brownish, pink, or yellow. There are sometimes small marginal tubercles on abdominal segments II-IV and small spinal tubercles on the head. The antennal tubercles are well developed, usually smooth with diverging inner sides. The median frontal tubercle is very small or absent. The antennae are about as long as the body or longer. Apterae have secondary rhinaria near the base of antennal segment III; alates have more rhinaria on III. The siphunculi are cylindrical or tapering, occasionally with 1-3 rows of hexagonal cells below the distinct flange. The cauda is tongue- or finger-shaped, often slightly constricted.

This is a genus of about 80 species worldwide living without host alternation on various dicotyledons, particularly Fabaceae, Rosaceae, and Euphorbiaceae.

 

Acyrthosiphon boreale (Northern cinquefoil aphid) Europe, Canada

Adult apterae of Acyrthosiphon boreale are green with the anterior part of the body yellowish. Their antennal tubercles are well developed with diverging, rough inner sides. The antennae are 0.7-1.1 the body length and the terminal process is 4.6- 6.0 times longer than the base of the sixth antennal segment. The third antennal segment of the aptera has 2-14 (rarely less than 5) slightly raised secondary rhinaria mainly on the basal half.The dorsal cuticle is slightly sclerotized and wrinkled, but not pigmented. The siphunculi are cylindrical with a rather well developed flange. The siphunculi are 0.21-0.30 times the body length and 1.5-2.6 times longer than the cauda. The cauda is rather thick, not constricted and bearing 7-11 hairs.

The fundatrix is similar to the aptera, but the terminal process is only 2.7 times longer than the base of the sixth antennal segment. Males are apterous.

Acyrthosiphon boreale lives year round on cinquefoils (Potentilla) species. It has a boreo-alpine distribution including northern Europe, Greenland and Canada.

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Acyrthosiphon caraganae (Caragana aphid) Asia, Europe, North America

Adult apterae of Acyrthosiphon caraganae (see pictures of colonies below) are green; in not too old specimens there are grey intersegmental wax strips (see here) and a bright green longitudinal dorsal stripe. The apices of antennae & siphunculi are dusky. Antennal tubercles have diverging inner sides, and the median frontal tubercle is low. Antennae are 1.0-1.2 times body length, with the terminal process 4-6 times the base of antennal segment VI. Antennal segment I is wider than it is long (cf. Acyrthosiphon gossypii & Acyrthosiphum pisum, both of which have antennal segment I longer than wide). Antennal segment III bears 1-6 secondary rhinaria. The rostrum reaches to just past the middle coxae; the apical rostral segment is 0.7-0.8 times the second hind tarsal segment, with 5-7 accessory hairs. First tarsal segments have 3-3-3 hairs (fore-mid-hind). Siphunculi are 0.25-0.33 times body length, and 1.5-2.1 times the cauda; mid-diameter of siphunculi is about 1.1-1.5 times mid-diameter of hind tibia (cf. Acyrthosiphum pisum, which has siphunculi thinner than hind tibiae at midlength). The cauda is slender, occasionally slightly constricted, with 7-10 hairs. Body length of adult Acyrthosiphon caraganae apterae is 2.6-4.3 mm.

First image above copyright Timofey Palkin, second image copyright Vadim Rybakov,
both under a creative common licence.

The alate vivipara of Acyrthosiphon caraganae (see clarified slide mount in second picture below) is green in life, with the siphunculi and apical halves of the antennae rather dark. The abdomen has no distinctly visible sclerites. The antennal terminal process is 5-6 times the base of antennal segment VI. Antennal segment III bears 6-24 secondary rhinaria, usually on the basal half only. The siphunculi and cauda are thinner than in the apterous female.

Subspecies

Several subspecies are recognised: Acyrthosiphon caraganae occidentale Hille Ris Lambers in western Europe, Acyrthosiphon caraganae tadzhikistanicum Narzikulov in Tajikistan and Acyrthosiphon caraganae sachalinense Pashchenko in Sakhalin Island, Russia.

Acyrthosiphon caraganae is monoecious on the leaves and young growth of woody Leguminosae, especially species of peashrub (Caragana) and bladder senna (Colutea), often forming large colonies. Populations are holocyclic, with apterous males in western Europe, but alate males in Russia, Switzerland and eastern Canada. Oviparae lay overwintering eggs on twigs of the host plant. Acyrthosiphon caraganae is thought to have originated in Mongolia, but it now occurs in parks and gardens in temperate regions throughout the Northern Hemisphere (North America, Europe, Asia).

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Acyrthosiphon chelidonii (Wax-dusted celandine aphid) Europe, central & east Asia

Adult apterae of Acyrthosiphon chelidonii (see first picture below) are pale green or greenish white, with a thin covering of greyish wax which is reduced along segmental borders (cf. Macrosiphum euphorbia, which has no covering of wax powder). The antennae are rather pale with darker apices, siphunculi are pale with dusky flanges, and the cauda is pale. Antennal tubercles are little developed, and the median frontal tubercle is flat. Antennae are 0.9-1.2 times body length, with the terminal process 2.7-3.3 times the base of antennal segment VI (cf. Aulacorthum solani, which has the terminal process 4.0-5.5 times as long as the base). Antennal segment III never has secondary rhinaria; the longest hairs on segment III are 0.5-0.6 times the basal diameter of that segment. The apical rostral segment is slender, and 0.8-0.9 times as long as the second hind tarsal segment. Body hairs are short. The dorsal cuticle is slightly sclerotic, somewhat scaly behind siphuncular bases. Siphunculi are about 0.19-0.28 times body length, and 1.7-2.3 times the cauda. The cauda is not constricted or only slightly so, tongue-shaped, rather short and blunt with 7-14 hairs. Body length of adult Acyrthosiphon chelidonii apterae is 1.5-2.3 mm.

Images above copyright Seo, H. et al., NIBR, The Aphids of Korea I,
under a Korea Open Government Licence.

The alate vivipara of Acyrthosiphon chelidonii (see second picture above) has a brownish thorax and a greenish abdomen, with very pale marginal sclerites; the siphunculi are pale with dark tips. Antennae are as long as the body with 5-13 secondary rhinaria on segment III. Siphunculi are 0.15-0.20 times body, and about 1.2 times cauda.

Acyrthosiphon chelidonii is monoecious on celandine, especially greater celandine (Chelidonium majus). They form colonies on the upper parts of stems and on young leaves (see picture above), where they are quite well camouflaged by their colour and grey wax powder. The species is holocyclic. Sexuales appear in October & November. Acyrthosiphon chelidonii has a wide distribution like its host plant, being found in Europe, central Asia, east Siberia, Korea and Japan.

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Acyrthosiphon cyparissiae (Dark-legged euphorbia aphid) Europe, Asia

Adult apterae of Acyrthosiphon cyparissiae (see first picture below) are green or less frequently brown. The front of the head is black, and in most of Europe they have mainly black appendages, but in warmer climates the appendages may be brown or brownish yellow (see below re. ssp. propinquum). The first tarsal segments have 5-7 hairs (cf. other Acyrthosiphon spp. on Euphorbia, which have 3 hairs on each first tarsal segment). The black siphunculi are long, thin and outwardly curving; they have no subapical polygonal reticulation, and no trace of swelling or constriction before the rather well-developed flange (cf. Macrosiphum euphorbiae, Macrosiphum euphorbiellum, and other Macrosiphum spp. on Euphorbia, which all have a zone of subapical polygonal reticulation on their siphunculi). The pale greenish-brown cauda is long and pointed. The body length of adult Acyrthosiphon cyparissiae apterae is 2.4-3.4 mm.

Both images above copyright Marko Šćiban, all rights reserved.

The alate Acyrthosiphon cyparissiae (see second picture above) has similar coloration to the aptera, with green and brown forms, apart from the thorax which is brown.

There are two subspecies:

  • Acyrthosiphon cyparissiae ssp. propinquum. This has the front of the head pale or dusky, and the antennae, tibiae and siphunculi mainly pale with only the apices dark. Blackman comments that this form may not be a true subspecies but merely an effect of the environment.
  • Acyrthosiphon cyparissiae ssp. turkestanicum, which has been recorded from several Euphorbia (Euphorbia esula ssp. tommasiniana, Euphorbia ferganensis, Euphorbia lamprocarpa) in Central Asia.

Acyrthosiphon cyparissiae feeds only on Euphorbia species - mainly on the upper sides of the upper leaves. Sexual forms develop in autumn with alate males. It is found in Europe (but not apparently in the UK), the Middle East, Central Asia and China. The observations reported here by Marko Sciban appear to represent the first on-host record of the species in Serbia.

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Acyrthosiphon gossypii (Cotton aphid) Asia, Europe, North Africa

Adult apterae of Acyrthosiphon gossypii are greenish (or sometimes yellowish), with adults and immatures dusted with fine wax (cf. Acyrthosiphon pisum, where adult apterae have no wax bloom and are therefore conspicuous in colonies). Their antennal tubercles are well developed, with their inner faces divergent. The antennae are almost 1.4 times as long as body, and the terminal process is 3-3.5 times as long the base of last antennal segment. They have 1 or 2 secondary rhinaria on antennal segment III. The siphunculi are pale and attenuated distally, thinner than the hind tibiae at their respective midpoints, and 2.5-3.5 times the length of the cauda (cf. Acyrthosiphon pisum, whose siphunculi are thin and cylindrical distally, 1.2-1.9 times the caudal length). The siphunculi have no subapical zone of polygonal reticulation (cf. Macrosiphum euphorbiae, which does have a subapical zone of polygonal reticulation on its siphunculi). The cauda is tongue-shaped and bears 3-6 hairs. The body length of adult Acyrthosiphon gossypii apterae is 2.5-3.8 mm.

Images above by permission, copyright Sunil Joshi & Poorani, J. Aphids of Karnataka. (accessed 12/8/20).

Acyrthosiphon gossypii alatae are coloured similar to the apterae, and bear 9-12 secondary rhinaria.

Acyrthosiphon gossypii is a warm-country species that feeds on members of the Fabaceae, especially various beans (Dolichos, Phaseolus, Vigna) as well as Malvaceae (including cotton and okra) and Zygophyllaceae (bean capers and caltrops). They have also been reported on certain trees such as the black locust (Robinia pseudacacia) and Japanese pagoda tree (Styphnolobium japonicum). It is a pest of cotton in central Asia. The species is anholocyclic over much of its range, but there is a holocycle on camelthorn (Alhagi camelorum) in central Asia. Its distribution extends from China and India through south-west and central Asia to the Middle East, North Africa, and parts of southern Europe.

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Acyrthosiphon kondoi (Blue alfalfa aphid) East Asia, North & South America, Australia

Adult apterae of Acyrthosiphon kondoi are bluish green. Their antennae are light brown basally, progressively darkening to the terminal process (cf. Acyrthosiphon pisum, invasive in America, which has dark bands at the apices of each antennal segment). The antennal terminal process is 4.7-6.0 times as long as the base of antennal segment VI (cf. Acyrthosiphon loti in Eurasia & South America, which has the terminal process 2.7-4.2 times the length of the base, and cf. Acyrthosiphon pisivorum (= ? Acyrthosiphon phaseoli) in China, whose terminal process is about 3 times as long as the base). The antennal terminal process is less than 0.2 mm long (cf. Acyrthosiphon pisum, which has a terminal process 0.25-0.40 mm long). The siphunculi are without a subapical zone of polygonal reticulation (cf. the cosmopolitan Macrosiphum euphorbiae & Macrosiphum creeli in North America, both of which a subapical zone of polygonal reticulation). The siphunculi are 1.6-2.1 times the caudal length (cf. Acyrthosiphon astragali in South Asia, which has siphunculi 2.0-2.6 times the length of the cauda, and cf. Acyrthosiphon gossypii in southern Europe and South Asia, which has siphunculi 2.5-3.5 times as long as the cauda). The siphunculi are only slightly attenuated distally (cf. Acyrthosiphon pisum, which has its siphunculi attenuated distally such that they are thinner than the hind tibiae at their respective midlengths).

Images above copyright Jesse Rorabaugh under a public domain (CCO) licence.

Alatae of Acyrthosiphon kondoi (see second picture above) have a darker brown thorax than Acyrthosiphon pisum, and have 7-9 secondary rhinaria confined to the basal half of antennal segment III.

Acyrthosiphon kondoi feeds on the stems and leaves of alfalfa (Medicago sativa), and other Medicago species, sweet clovers (Melilotus spp.), clovers (Trifolium spp.) and canary clovers (Dorycnium & Lotus spp.) as well as on milkvetches (Astragalus spp) and some members of the pea & bean family (Fabaceae). In its native Japan Acyrthosiphon kondoi is monoecious holocyclic, but seems to be anholocyclic in most other places. It is an important pest of alfalfa, most notably where it is invasive such as North and South America, South Africa, Australia and New Zealand.

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Acyrthosiphon lactucae (Lettuce seed-stem aphid) Europe, Asia, North & South America

Adult apterae of Acyrthosiphon lactucae (see first picture below) are pale yellowish green or pink. The dorsal surface has a pale grey wax bloom, often appearing as pale transverse stripes. The head is smooth, and the antennal tubercles are well developed with smooth broadly-divergent inner faces. The terminal process is less than 7.5 times as long as the base of antennal segment VI. Antennal segment III has secondary rhinaria and bears hairs that are less than 0.7 times the diameter of that segment. The fused apical rostral segment (R IV+V) is 0.6-0.7 times the length of the second hind tarsal segment (HTII), and has 16-25 accessory hairs (cf. Acyrthosiphon ilka, which has RIV+V 0.8-0.9 times the length of HTII, with 6-8 accessory hairs). There are no dark markings on the dorsum (cf. Nasonovia ribisnigri, which on the secondary host - lettuce - has dark intersegmental sclerites between each abdominal segment). Abdominal tergites I and VII usually have no marginal tubercles. The siphunculi are long and tapering with no polygonal reticulation (cf. Hyperomyzus lactucae, which has distinctly swollen siphunculi). The cauda is finger-shaped, clearly longer than its basal length. The body length of adult apterae is 1.7-2.9 mm. Immature apterous Acyrthosiphon lactucae (see second picture below) resemble the adult apterae, but have shorter siphunculi and cauda.

Both images above by permission, copyright Claude Pilon, all rights reserved.

Acyrthosiphon lactucae alatae (see second picture above of immature and adult alate of the pink form) show the same two colour forms as the apterae, but have somewhat dusky siphunculi.

Acyrthosiphon lactucae feeds on stems and undersides of leaves of lettuce (Lactuca species). It does not host alternate, remaining on lettuce year round. Sexuales develop in autumn, with alate males. Acyrthosiphon lactucae is a native Eurasian species and is found throughout Europe, the Middle East, Kazakhstan and Pakistan. In Britain the lettuce seed-stem aphid has only been found in southern counties. It was introduced to North America many years ago and is now widely distributed there. More recently Acyrthosiphon lactucae has been recorded from Argentina and Chile.

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Acyrthosiphon loti (Green trefoil aphid) Europe, South America

Apterae of Acyrthosiphon loti are green, or rarely pink, often with indistinct greyish transverse stripes. Their antennae have dark apices, but the individual antennal segments do not have dark apices. The antennae are 0.9-1.0 times the body length, and the antennal terminal process is 3.2-4.0 times longer than the base. The antennal tubercles of Acyrthosiphon loti are low and smooth and strongly diverging. The median frontal tubercle is low and flat. Acyrthosiphon loti siphunculi are dark tipped and are 1.2-1.6 times the caudal length. The siphuncular diameter at the midpoint is 1.0-1.4 times the diameter of the hind tibia at its midpoint. The body length of Acyrthosiphon loti is 1.7 to 2.9 mm.

The alate has rather indistinct marginal sclerites and pleural intersegmental sclerites. The third antennal segment has 3-19 rather large rhinaria, and the siphunculi are thinner than in the apterae. The apterous male Acyrthosiphon loti is greyish red with a very slender body.

The green trefoil aphid does not host alternate. Sexual forms occur in autumn and males are apterous or alate. It feeds on various members of the pea family (Fabaceae) especially trefoils (Lotus, Anthyllis and Hippocrepis) and lucerne (also known as alfalfa, Medicago sativa). Acyrthosiphon loti is found in Europe, eastward to Turkey, and has been introduced to Argentina.

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Acyrthosiphon macrosiphum (Long-legged serviceberry aphid) North America

Adult apterae of Acyrthosiphon macrosiphum have an amber-yellow head and the rest of the dorsum yellow-green to green (the picture below shows a fundatrix, which appears to be more yellowish than the apterous vivipara). Antennal segments I to the middle of III are pale, but the distal segments are dusky to blackish. The rostrum reaches the second coxae. The apical rostral segment (RIV+V) is shorter than the length of the second hind tarsal segment. The tibiae are light brown, darker at knees and tips. The siphunculi have a broad base, but narrow rapidly to become more or less cylindrical; they are without reticulation. The siphunculi are very long, longer than antennal segment III, and about twice the length of antennal segment IV. The cauda and anal plate are pale. The cauda is parallel-sided to tapering, and bears two lateral pairs of hairs and 3-4 dorsal or dorsolateral hairs. The body length of adult Acyrthosiphon macrosiphum apterae is 1.5-1.9 mm.

First image above copyright Andrew Jensen; second image above above copyright CBG Photography Group
both under a Creative Commons License.

The alate vivipara (second picture above) of Acyrthosiphon macrosiphum is similar to the apterous vivipara, but with a brownish head and thorax. The abdomen is yellow green. The rostrum hardly reaches the second coxae. The siphunculi are pale to light dusky, without reticulation. There are 19-44 secondary rhinaria on antennal segment III.

Acyrthosiphon macrosiphum is monoecious, feeding on the leaves of serviceberry (Amelanchier spp.) and possibly American elder (Sambucus canadensis). The species is found on different Amelanchier species in a range of habitats from moist forests to riparian habitats to deserts. Jensen, in aphidtrek, notes that in desert this species has a quite different appearance with lateral green stripes on the head and thorax, albeit there were no obvious morphological differences between desert- and forest-inhabiting populations. Acyrthosiphon macrosiphum is holocyclic, with sexuales recorded in September and October. It seems to be restricted to the western states of the USA (California, Colorado, Utah, Oregon, Montana) and western Canada (British Columbia, Saskatchewan).

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Acyrthosiphon malvae (Geranium aphid, Pelargonium aphid) Cosmopolitan

Acyrthosiphon malvae apterae are green, yellowish or greyish green, or pinkish red (see first two pictures below). The femora and siphunculi are pale. The terminal process of antennal segment VI is 4.8-5.8 times the length of its base. The longest hair on antennal segment III is 0.7-1.0 times the diameter of that segment and the apterae have 1-24 secondary rhinaria on that segment. The fused apical rostral segments are 1.1-1.4 times the second hind tarsal segment. Their siphunculi have no polygonal reticulation, are cylindrical on the distal half and are 1.8-2.2 times the pale caudal length. The body length is 1.5-3.2 mm.

The alate Acyrthosiphon malvae (shown giving birth in third picture above) has antennae longer than the body with 12-31 secondary rhinaria on antennal segment III. The abdomen is usually unsclerotized but may have small spinal and intersegmental pleural sclerites. The siphunculi and cauda are more slender than in the apterae.

Acyrthosiphon malvae is found on many plants, but particularly herbaceous Rosaceae. There are many subspecies, mostly with specific host-plant associations.

  1. Acyrthosiphon malvae sensu stricto are pale green or red aphids on many Geraniaceae and Malvaceae worldwide, as well as plants in other families.
  2. Acyrthosiphon malvae subspecies agrimoniae is yellowish green and found in flowerheads or on undersides of leaves of Agrimonia species (agrimony) in Europe and western Asia.
  3. Acyrthosiphon malvae subspecies poterii is bright salmon pink, yellowish or green and found on Poterium sanguisorba (= Sanguisorba minor) (salad burnet), and is only known from England.
  4. Acyrthosiphon malvae subspecies potha Börner is pale yellowish or greyish green and associated with Alchemilla species (lady's mantle) throughout Europe.
  5. Acyrthosiphon malvae subspecies rogersii (Theobald) is green or yellow-green, often shiny, and may form large colonies on young leaves of Fragaria (strawberry) in north and west Europe (Blackman & Eastop 2006).

The geranium aphid does not host alternate. All subspecies spend their entire life cycles on their respective host plants, overwintering in the egg stage. Distribution varies according to subspecies (see above).

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Acyrthosiphon pisum (Pea aphid) Cosmopolitan

Acyrthosiphon pisum apterae (see first picture below) are pale green or pink with red eyes. The antennae of Acyrthosiphon pisum are 1.0-1.6 times as long as the body. The antennal segments, tibiae and siphunculi have dark apices (cf. Acyrthosiphon loti which does not have the antennal joints darkened). The siphunculi are tapering and very thin with the diameter of a siphunculus in the middle less than the diameter of the hind tibia; the siphunculi are 1.2-1.9 times the length of the cauda. The cauda is long and tapered. The body length of Acyrthosiphon pisum apterae ranges from 2.2 to 5.0 mm long.

The alate viviparous female (see second picture above) has the head and thorax only slightly darker than the abdomen which is pale with small marginal sclerites.

The pea aphid can be found feeding on about 20 genera in the family Fabaceae but especially on Medicago, Melilotus, Trifolium, Dorycnium and Lotus. Acyrthosiphon pisum is a major pest of peas and alfalfa, partly because of direct feeding damage and partly because of virus transmission. Adults readily fall to the ground if the plant is disturbed. The pea aphid is found worldwide in temperate climates.

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Acyrthosiphon primulae (Primrose aphid) Europe, North America

Adult apterae of Acyrthosiphon primulae (see first picture below) are shiny pale yellow to greenish yellow. They have dark tips to the antennae and legs, but not to the siphunculi which are entirely pale. The median frontal tubercle is slightly developed. The siphunculi are 2.2-3.1 times longer than the cauda. The cauda of Acyrthosiphon primulae is 1.3-1.6 times longer than the base of antennal segment 6 (cf. Acyrthosiphon malvae which has the cauda 1.8-2.6 times longer than the base of antennal segment 6).

The Acyrthosiphon primulae alate vivipara (see second picture above) has dark distal cross-bands and postsiphuncular sclerites.

Acyrthosiphon primulae lives on the underside of leaves of Primula species, especially cowslip (Primula veris) and Kew primrose (Primula X kewensis). It reproduces solely by parthenogenesis and no sexual forms are known. Acyrthosiphon primulae is found in Britain and some European countries, and has been introduced to Tasmania, New Zealand and California.

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Acyrthosiphon purshiae (Bitterbrush aphid) North America

Adult apterae of Acyrthosiphon purshiae (see first picture below) have the entire dorsum medium green, either slightly frosted or shining. Antennal segments I and III, the cauda and femora are pale brown, but all other parts of their appendages are black (cf. Acyrthosiphon malvae, which has mainly pale appendages). Their hairs are blunt; on the proximal half of antennal segment III they are 0.05 mm long. The apical rostral segment (RIV+V) is triangular, almost acute, hardly reaching the third pair of coxae, and less than 0.9 times the length of the second hind tarsal segment (HTII) (cf. Acyrthosiphon malvae, which has RIV+V more than 0.9 times HTII). The siphunculi are elongate, tapering, imbricated, not reticulated, and with a flange. The cauda is elongate, tapering, with scarcely any tendency to constriction at the base, and has three hairs on each side. The body length of adult Acyrthosiphon purshiae apterae is 2.0-2.5 mm.

Note: Acyrthosiphon purshiae was first described by Palmer (1938) in the genus Macrosiphum. Blackman suggests that that it should probably be returned to that genus given the DNA analysis by Foottit et al. (2008).

First image above copyright Andrew Jensen under a cc by-nc-sa licence;
Second image above copyright Walter Siegmund under a cc by-sa licence.

The alate Acyrthosiphon purshiae is presumably green, but we have found no description nor photo of the alate morph.

Acyrthosiphon purshiae is found on the leaves and stems of bitterbrush Purshia tridentata (see second picture above). Jensen noted that although bitterbrush is widespread and common in many dry habitats of the interior western North America, the aphid is not so common, only occurring in certain partially-forested areas where bitterbrush grows. The species is monoecious holocyclic, and is restricted to the western USA and British Columbia, Canada.

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Acknowledgements

Whilst we make every effort to ensure that identifications are correct, we cannot absolutely warranty their accuracy. We have mostly made identifications from high resolution photos of living specimens, along with host plant identity. In the great majority of cases, identifications have been confirmed by microscopic examination of preserved specimens. We have used the keys and species accounts of Blackman & Eastop (1994) and Blackman & Eastop (2006) supplemented with Blackman (1974), Stroyan (1977), Stroyan (1984), Blackman & Eastop (1984), Heie (1980-1995), Dixon & Thieme (2007) and Blackman (2010). We fully acknowledge these authors as the source for the (summarized) taxonomic information we have presented. Any errors in identification or information are ours alone, and we would be very grateful for any corrections. For assistance on the terms used for aphid morphology we suggest the figure provided by Blackman & Eastop (2006).

Useful weblinks

References

  •  Blackman, R.L. & Eastop, V.F. (2006). Aphids on the world's herbaceous plants and shrubs. Vols 1 and 2. John Wiley & Sons.