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Aphididae : Aphidinae : Aphidini : Pseudasiphonaphis
 

 

Genus Pseudasiphonaphis

Pseudasiphonaphis aphids

On this page: Pseudasiphonaphis corni

Pseudasiphonaphis [Macrosiphini]

Pseudasiphonaphis aphids have extensive wax secretion. Antennal and median frontal tubercles are absent. Hairs on antennal segments are long (up to 0.07 mm) on apterae, but short (up to 0.03 mm) on alatae. In the alate the second fork of the media vein in the fore wing is very close to the wing margin, and is sometimes absent. Chaetotaxy (=arrangement) of hairs on first tarsal segments is 3-3-2, occasionally 3-3-3 (fore-mid-hind). On the abdomen, the marginal tubercles are slender, about twice as long as wide; those on abdominal tergites I and VII are toward the dorsal side of the stigmata. The siphunculi are very small, inconspicuous, not more than two-thirds of their width long, and flangeless with narrow pores; they are situated between tergites V and VI.

The genus Pseudasiphonaphis has only one species, which is now believed to host alternate from the primary host, dogwood (Cornus) to its secondary host, clearweed (Pilea) and skullcaps (Scutellaria).

 

Pseudasiphonaphis corni (Waxy dogwood aphid) Eastern North America

Adult apterae of Pseudasiphonaphis corni (see first picture below) are a fairly uniform reddish brown, covered in an extensive light greyish-white woolly wax secretion. The head is rounded in front, with no antennal tubercles. The antennae are light brown, slightly shorter than the body, with a few rather prominent fine hairs about 2-3 times as long as the width of segment III. The antennae have no secondary rhinaria. The terminal process is about 1.4 times the base of antennal segment VI (cf. Anoecia corni on Cornus, whose terminal process is less than 0.5 times the base of segment VI) . The rostrum reaches to the third pair of coxae. The entire dorsum is covered with wax glands. The prothorax and abdominal tergites I-VII bear prominent, toothlike marginal tubercles. The siphunculi are very small, papillate (= nipple-like), and inconspicuous, though visible in freshly mounted specimens (cf. Aphis gossypii and various Myzus spp. on other Pilea & Scutellaria spp., which have cylindrical or slightly swollen siphunculi). The cauda is brown, long, broad and tapering with about four rather prominent hairs on each side, with the terminal pair of hairs strongly incurved. The body length of adult Pseudasiphonaphis corni apterae is 1.7-2.1 mm.

Images above copyright Charley Eiseman, under a Creative Commons Attribution License.

The alate Pseudasiphonaphis corni has a very prominent median ocellus, and rather large ocular tubercles. The antennae are uniformly brown throughout. Antennal segment III has 7-10 more-or-less circular secondary rhinaria, which are very irregular in size and in a generally straight row over most of the length of the segment. Antennal segment IV has 0 to 2 rhinaria, and segment V has none. The rostrum reaches to the third pair of coxae. The wings are hyaline, the veins dark brown or black, and the stigma dusky. The abdomen is a uniform reddish-brown. The siphunculi are slightly larger and more conspicuous than those on the aptera.

Tissot (1929), who first described this species, describes how a few colonies of this aphid were found in April feeding on the underside of the leaves, and along the tender shoots of a toughleaf dogwood (Cornus asperifolia = Cornus microcarpa). Numbers decreased in summer but they were never entirely absent, which would seem to indicate that they did not host alternate. In autumn no sexual forms were observed, and it was assumed that, at least in Florida, populations were anholocyclic. However, in the 1960s, Robinson (1965) reported that Pseudasiphonaphis corni (as Asiphonaphis anogis) had been found further north in the United States on clearweed (Pilea pumila, in the Urticaceae) and mad-dog skullcap (Scutellaria lateriflora, in the Lamiaceae). Also Asiphonaphis anogis was synonomized with Pseudasiphonaphis corni, and Hottes & Frison (1931) had reported alate males of that species being found in October on Pilea. Robinson (1967) therefore concluded that they were host alternating between Cornus, as the primary host, and Pilea/Scutellaria, as the secondary hosts. This is the currently accepted life cycle, albeit there are no records of the return migration to Cornus. Pseudasiphonaphis corni is found in eastern USA and Canada.

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Acknowledgements

We are grateful to Charley Eiseman for making his images of Pseudasiphonaphis corni available for use under creative commons licences.

We have used the keys and species accounts of Tissot (1929) (as Pergandeidia corni), Hottes & Frison (1931) (as Asiphonaphis anogis), Robinson (1965)(as Pseudasiphonaphis anogis), and Robinson (1967) together with information from Roger Blackman & Victor Eastop in Aphids on Worlds Plants. We fully acknowledge these authors as the source for the (summarized) taxonomic information we have presented. Any errors in 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).

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References

  • Hottes, F.C. & Frison, T.H. (1931). The Plant Lice, or Aphiidae, of Illinois. Illinois Natural History Survey Bulletin 19(3), 123-447. (p. 225) Full text

  • Robinson, A.G. (1965). A new genus, new species and previously undescribed morphs of aphids (Homoptera : Aphididae). The Canadian Entomologist 97 1009-1015.

  • Robinson, A.G. (1967). A new genus Misturaphis and a new species of Cryptaphis from Manitoba (Homoptera: Aphididae) with a note on Pseudasiphonaphis anogis. The Canadian Entomologist 99(6), 565-569 (p. 569)

  • Tissot, A.N. (1929). A new dogwood aphid from Florida. Florida Entomologist 13(1), 1-4 (p. 2) Full text