Clethrobius comes

Identification & Distribution:

All adult viviparous female Clethrobius comes are winged. Freshly moulted viviparae of Clethrobius comes (see first picture below) are light brown, but matured adult alatae (see second picture below) are dark brown or greenish black. The scleroites as far back as tergite VI bear groups of wax pore facets, producing bands of light wax pulverulence (see second picture below). The marginal sclerites on tergites I-IV are produced into blunt rounded prominences bearing 2-3 marginal hairs each. The antennae, legs and cauda are black, apart from the bases of the femurs which are pale. The antennae are much shorter than the body, with a terminal process that is 0.67-0.75 times the length of the base of the last antennal segment. The rostrum is very short, hardly or just reaching the middle coxae. The siphunculi are dark sclerotic, shortly conical, in length about 0.6 times their basal width. The cauda is knobbed and distinctly constricted. The body length of winged Clethrobius comes viviparae is 4.1-4.4 mm.

The hairy birch aphid forms clusters on branches and twigs of birch (Betula spp.), often where the new growth is dying back, or on twigs of alder (Alnus spp.) overhanging streams. The populations on alder are regarded by some as a separate species, Clethrobius giganteus, and attempts to transfer aphids from birch to alder have not succeeded. However, no consistent morphological differences have been found. Sexual forms develop in October-November. Clethrobius comes occurs throughout Europe and across Asia to China, Korea and Japan.

Biology & Ecology:

In the literature the hairy birch aphid is recorded as being rare in the UK. We have found the brown hairy birch aphid not uncommonly on birch in southern England in locations in Surrey, Hampshire, and East Sussex. We first encountered a small colony of Clethrobius comes at Warnham Common in Surrey comprising an alate with a few nymphs. The youngest nymphs (see picture below) are greenish in colour.

We encountered a much bigger colony on a damaged branch of silver birch in a marshy area of the New Forest in Hampshire. Many of the nymphs had reached the fourth instar stage, shown below.

By the fourth instar, all the nymphs are brown and in this particular colony all were alatiform. The preponderance of alatiform nymphs probably resulted from the declining nutritional quality of the branch that the aphids were feeding on. A few had moulted to the adult alate form (see picture below).

Hille Ris Lambers (1947) records that colonies of this species may reach enormous numbers. Large aphid colonies usually attract aphid predators, and this one was no exception. The picture below shows several syrphid eggs laid amongst the colony.

Michalik (2010) describes endosymbionts (Buchnera aphidicola) found in Clethrobius comes. These endosymbionts provide their hosts with essential amino acids which are absent in phloem sap of plants. Endosymbionts are transovarially transmitted from mother to offspring. In the oviparous generations bacteria were found to infect choriogenic oocytes, whereas in the oviparous generations they were found to infest young embryos.

Other aphids on same host:

Blackman & Eastop list about 72 species of aphids as feeding on birches worldwide, and provides formal identification keys for aphids on Betula.

• Blackman & Eastop list 17 species of aphids feeding on Betula pendula worldwide (Show World list). Of these, Baker (2015) lists 14 as occurring in Britain (Show British list).

  Blackman & Eastop list 15 species of aphids feeding on Betula pubescens (Show World list). Of these, Baker (2015) lists 14 as occurring in Britain (Show British list).

• Blackman & Eastop list 8 species of aphids as feeding on common alder (Alnus glutinosa) worldwide, and provides formal identification keys for aphids on Alnus. (Show World list). Of those, Baker (2015) lists 7 aphid species as occurring in Britain (Show British list).

Acknowledgements We especially thank Warnham Common Nature Reserve for their kind assistance, and permission to sample. 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 Michalik, A. (2010). Ovary structure and transovarial transmission of endosymbiotic microorganisms in Clethrobius comes, Myzocallis walshii and Sipha maydis /Hemiptera, Aphididae: Drepanosiphinae/. Aphids and other Hemipterous Insects 16 (1), 5-12. Full text Hille Ris Lambers, D. (1947). On some mainly Western European aphids. Zoologische Mededeelingen 28, 291-333. Full text