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Dysaphis pyri

Pear-bedstraw aphid

On this page: Identification & Distribution Biology & Ecology Damage & Control

Identification & Distribution:

Dysaphis pyri induce yellowed pseudogalls on Pyrus (pear) in spring (see first picture below). Adult apterae of Dysaphis pyri are medium to rather large globe-shaped, brownish-red to dark brown aphids, thickly coated with grey wax meal (see second picture below). The antennae are pale yellow near the base, but darker towards the apex. The first 5 abdominal tergites have a double row of small dark spots. Hemispherical marginal tubercles are usually present only on abdominal tergites 1-5. The siphunculi are black and perpendicular to the body. They are 3.4-4.1 times their diameter at midpoint, and longer than the cone-shaped cauda. The adult aptera has a body length of 2.1-3.2 mm. Immature Dysaphis pyri are a pale yellowish brown, with reddish suffusion around the bases of their siphunculi (see third picture below).

Spring migrant alates have the abdomen brownish-red with a black dorsal patch. They have 23-36 secondary rhinaria on antennal segment III, 2-10 on segment IV and 0-1 on segment V.

The clarified slide mounts below are of adult viviparous female Dysaphis pyri : wingless on primary host, and winged spring migrant.

Micrographs of clarified mounts by permission of Roger Blackman, copyright AWP all rights reserved.

The primary host of Dysaphis pyri is common pear (Pyrus communis). Leaves and shoots are yellowed and distorted to form a pseudogall. After about three generations on pear, alatae are produced which migrate to the secondary hosts. These are bedstraws, especially hedge bedstraw (Galium mollugo) and cleavers (Galium aparine) and sometimes squincywort (Asperula cynanchica). Dysaphis pyri may form colonies on the roots and prostrate stems, where it is attended by ants. Dysaphis pyri is found throughout Europe, the Middle East, North Africa and Central and South Asia, and has been introduced into the USA.

 

Biology & Ecology:

Savary (1953) studied the life history and population biology of Dysaphis pyri in Switzerland.

Dysaphis pyri sometimes 'shares' its pseudogalls with other aphids. The picture above shows a mixed colony of Dysaphis pyri and Rhopalosiphum oxyacanthae - the latter are the small green aphids.

The aphid below appears to be an aberrant specimen of Dysaphis pyri which has not developed its wax coating. The smaller aphids are its nymphs.

The only predators we have so far found attacking Dysaphis pyri within the pseudogall are syrphid larvae such as the one shown below.

Rojo & Marcos-Garcia. (1997) looked at syrphid predators of pear tree aphid pests. Larvae of the pipizine syrphid Heringia heringii were more abundant than those of other syrphid species. More than 40% of Heringia heringii larvae were collected on Dysaphis pyri colonies.

Rakauskas (2004) reported the appearance of large numbers of Dysaphis pyri necessitating chemical control in Lithuania in 2002. Aphids could not be found on the summer host Galium. so it was concluded these were probably airborne summer migrants, possibly the result of global warming.

 

Other aphids on same host:

Primary host

Dysaphis pyri has been recorded from 8 Pyrus species.

Blackman & Eastop list 53 species of aphid as feeding on common pear (Pyrus communis) worldwide, and provide formal identification keys.

Of those aphid species, Baker (2015) lists 29 as occurring in Britain: Anuraphis catonii, Anuraphis farfarae, Anuraphis subterranea, Aphis craccivora, Aphis fabae, Aphis gossypii, Aphis pomi, Aphis solanella, Aphis spiraecola, Aulacorthum solani, Brachycaudus cardui, Brachycaudus helichrysi, Brachycaudus persicae, Dysaphis plantaginea, Dysaphis pyri, Eriosoma flavum, Eriosoma lanigerum, Eriosoma lanuginosum, Eriosoma pyricola, Macrosiphum euphorbiae, Macrosiphum rosae, Melanaphis pyraria, Myzus ornatus, Myzus persicae, Nearctaphis bakeri, Ovatus crataegarius, Ovatus insitus, Rhopalosiphum oxyacanthae and Rhopalosiphum padi.

Secondary hosts

 

Damage and control

Dysaphis pyri is the most important aphid pest of pear causing severe direct feeding damage to both shoots and fruits. Growing shoots and leaves are distorted and yellowed, and heavy infestations check plant growth. Large quantities of honeydew are produced, further affecting growth.

Insecticide treatment is still the primary method of control. Alford (ed) (2000) recommends application of insecticides if any Dysaphis pyri are detected before flowering. From petal fall onwards, a suitable threshold is if 1% of trees is infested. Suitable insecticides include the organophosphates chlorpyrifos and dimethoate, the pyrethroid cypermethrin, the alkaloid insecticide nicotine, soap concentrate containing fatty acids and rotenone. A tar oil winter wash can be used against overwintering eggs.

Sauphanor et al. (1993) carried out a field trial to test the nontarget effects of pesticides on beneficial insects in a pear orchard near Avignon, France. The treatments were applied in April and May to affect the first generation of another pest, Dasineura pyri. Observations were carried out for 15 days after each of the treatments (amitraz, diazinon and pyrethrins + rotenone) to study the effect on Psylla pyri, Dysaphis pyri, and the main natural enemies present. It was concluded that earwigs (Forficula auricularia) play a major role in the regulation of Psylla pyri populations.

So far no resistant varieties of pear have been developed, although Evans et al. (2008) has identified a new gene for resistance to the aphid.

Cross et al. (1999) reviewed biocontrol of pests of apples and pears by parasitoids in central and northern Europe. Only Ephedrus persicae , a species specialising in leaf-curling aphids in trees, is recorded as attacking Dysaphis pyri and then only at a low level of effectiveness. It is suggested that host plant alternation may diminish the effectiveness of parasitoids for Dysaphis pyri.

Acknowledgements

Our particular thanks to Roger Blackman for images of his clarified slide mounts.

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

  • Alford, D.V. (2000). Pest and Disease Management Handbook. Blackwell, Oxford.

  • Cross, J.V. et al. (1999). Biocontrol of pests of apples and pears in Northern and Central Europe: 2. Parasitoids. Biocontrol Science and Technology 9, 277-314. Full text

  • Evans, K. et al. (2008). A new gene for resistance to Dysaphis pyri in pear and identification of flanking microsatellite markers. Genome 51(12), 1026-1031.  Abstract

  • Rakauskas, R. (2004). Recent changes in aphid (Hemiptera, Sternorrhyncha: Aphididae) fauna of Lithuania: an effect of global warming. Ekologija 1, 1-4. Full text

  • Rojo, S. & Marcos-Garcia, M.A. (1997). Syrphid predators (Dipt.: Syrphidae) of gall forming aphids (Hom.: Aphididae) in Mediterranean areas: Implications for biological control of fruit trees pests. Entomophaga 42(1/2), 269-276. Full text

  • Sauphanor, B. et al. (1993). Mean term effects of pesticides on beneficials in pear orchards: a field trial evaluation. Journal of Applied Entomology 116(5), 467-478.  Abstract

  • Savary, A. (1953). Le puceron cendre du poirer (Sapaphis pyri Fonsc.) en Suisse romande. Landwirtschaftliches Jahrbuch der Schweiz 67, 247-314.