Changes in green peach aphid responses to potato leafroll virus-induced volatiles emitted during disease progression.

Previous research has shown that green peach aphids, Myzus persicae (Sulzer), preferentially settle on leaflets of potato plants (Solanum tuberosum L.) infected with potato leafroll virus (PLRV) compared with sham-inoculated controls, at least in part because of aphid responses to volatile cues from the plants. The prior work used plants 4 wk after inoculation.

Parasitism of Lygus spp. nymphs by the parasitoid wasp, Peristenus howardi, in the alfalfa seed-growing region of the Pacific Northwest.

The parasitoid, Peristenus howardi Shaw (Hymenoptera: Braconidae) has been found to parasitize a large proportion of Lygus species in some Washington and Idaho alfalfa seed fields. During 2002-2003 a survey was conducted to estimate the proportion of Lygus spp. (Hemiptera: Miridae) parasitized and the amountof that parasitism attributable to P.

Influence of the Potato leafroll virus and virus-infected plants on the arrestment of the aphid, Myzus persicae.

A series of experiments was conducted using membrane sachets containing MP148 diet or phosphate-buffered sucrose with and without purified Potato leafroll virus to determine if direct encounter with the virus would arrest the aphid, Myzus persicae (Sulzer) (Homoptera: Aphididae). In only two out of 36 tests were there significantly more aphids settled on sachets containing the virus. In all other tests, there were either significantly fewer aphids on sachets containing virus or there were no differences between virus treatments and control sachets without virus.

Distinguishing the parasitic wasp, Peristenus howardi, from some of its congeners using polymerase chain reaction and restriction endonuclease digestion.

A molecular procedure incorporating polymerase chain reaction (PCR) of the COI gene and restriction endonuclease digestion of PCR products was used to distinguish Peristenus howardi (Hymenoptera: Braconidae) from four other Peristenus species. Non-solvent extraction of parasite DNA using a commercially available kit proved to be very effective in producing amplifiable template. Use of SfcI endonuclease produced restriction fragments with banding patterns in agarose gel electrophoresis that readily separated P.