Toni M. Withers

Potential of Selective Insecticides for Managing Uraba lugens (Lepidoptera: Nolidae) on Eucalypts

The leaf skeletonizer Uraba lugens Walker (Lepidoptera: Nolidae), an Australian species, locally known as gumleaf skeletonizer, is well established in New Zealand. This insect has the potential to become a serious pest of forestry and amenity eucalypts (Eucalyptus spp.) and is the focus of a long-term management program. The use of synthetic chemical or biological insecticides is one possible control method within an integrated control program. A series of dose-response trials were conducted using laboratory bioassays to test the efficacy of several insecticides against U. lugens: pyrethroids, spinosad, Bacillus thuringiensis kurstaki Berliner (Btk) and an insect growth regulator, Mimic. Pyrethroids and spinosad proved highly effective against U. lugens larvae, achieving 100% mortality after 3-6-d exposure. The performance of Btk was lower against gregarious skeletonizing larvae compared with solitary chewing larvae. When good coverage of the target foliage is achieved, >90% mortality is possible with Btk. Mimic performed poorly against U. lugens compared with other insecticides tested (<60% mortality). The Eucalyptus species on which larvae were feeding significantly altered insecticide efficacy. Treatments applied to Eucalyptus nitens (Deane & Maiden) Maiden had reduced efficacy compared with E. cinerea F. Muell. ex Benth. or E. fastigata Deane & Maiden. Cooler temperatures also reduced insecticide efficacy, presumably by decreasing movement and food consumption by U. lugens. Recommendations on spray applications to control U. lugens in New Zealand are given.

Post-release investigations into the fi eld host range of the gorse pod moth Cydia succedana Denis & Schiffermüller (Lepidoptera: Tortricidae) in New Zealand

The gorse pod moth Cydia succedana was released in New Zealand as a biological control agent against gorse Ulex europaeus L. in 1992 and is now widely established. Post-release evaluations of the host range of C. succedana were undertaken using both laboratory assays and field collections on native and exotic plants related to gorse. Field surveys did not detect any attack on native New Zealand plant species. However, contrary to predictions based on pre-release host-range testing, several species of exotic Genisteae, including Scotch broom Cytisus scoparius, Montpellier broom Teline (Genista) monspessulana, and tree lupin Lupinus arboreus, as well as lotus Lotus pedunculatus (Loteae) growing in the vicinity of infested U. europaeus plants, were shown to be hosts of C. succedana in both the North and South Islands of New Zealand. Hypotheses to explain this unexpected non-target attack include a seasonal asynchrony between C. succedana and gorse fl owering phenology, or that the original biocontrol introduction accidentally consisted of either two cryptic species or two populations with different physiological host range.

A laboratory rearing method for Cleopus japonicus (Wingelmüller) (Coleoptera: Curculionidae), a biological control agent for Buddleja davidii Franchet (Lamiales: Scrophulariaceae) in New Zealand

Buddleia, Buddleja davidii, is a fast-growing woody weed in New Zealand. The buddleia leaf weevil Cleopus japonicus was released in 2006 as a classical biological control agent for buddleia and is now established in the North Island. The laboratory rearing method developed and a morphological method of sexing the adults of this external leaf-feeding weevil are described.

Risk posed by the invasive defoliator Uraba lugens to New Zealand native flora

1 The risk posed to New Zealand native flora by the recently‐established pest of Australian origin Uraba lugens Walker (Lepidoptera: Nolidae) (gum leaf skeletonizer) was assessed. Weed biological control host range testing methods were applied to identify those New Zealand plant species potentially at risk. Native plants tested were primarily in the Myrtaceae, the family that contains all the Australian hosts of U. lugens. 2 Experimental methods included no‐choice larval feeding assays and field cage and laboratory oviposition trials. Difficulty in ascertaining reliable oviposition preference data from cage oviposition trials limited the confidence with which the invaders field host range could be predicted. 3 Field surveys of plants attacked by U. lugens in the infested area supported the initial predictions but only some of the at‐risk native Myrtaceae were present in the area. 4 The risk to native New Zealand plants is presented in terms of two mechanisms: development of self‐sustaining populations and temporary spill‐over of solitary larvae. Development of self‐sustaining populations of the pest within native forests is deemed to be highly improbable. 5 Temporary spill‐over impacts are most likely in urban areas within mixed species plantings or boundaries between native/exotic forests and coinciding with the mobile larval life stages. Spill‐over impacts from U. lugens have only been recorded to date on Metrosideros excelsa.

Identification of olfactory receptor neurons in Uraba lugens (Lepidoptera: Nolidae) and its implications for host range.

Phytophagous insects detect volatile compounds produced by host and non-host plants, using species-specific sets of olfactory receptor neurons (ORNs). To investigate the relationship between the range of host plants and the profile of ORNs, single sensillum recordings were carried out to identify ORNs and corresponding active compounds in female Uraba lugens (Lepidoptera: Nolidae), an oligophagous eucalypt feeder. Based on the response profiles to 39 plant volatile compounds, 13 classes of sensilla containing 40 classes of ORNs were identified in female U. lugens. More than 95% (163 out of 171) of these sensilla contained 16 classes of ORNs with narrow response spectra, and 62.6% (107 out of 171) 18 classes of ORNs with broad response spectra. Among the specialized ORNs, seven classes of ORNs exhibited high specificity to 1,8-cineole, (±)-citronellal, myrcene, (±)-linalool and (E)-β-caryophyllene, major volatiles produced by eucalypts, while nine other classes of ORNs showed highly specialized responses to green leaf volatiles, germacrene D, (E)-β-farnesene and geranyl acetate that are not produced by most eucalypts. We hypothesize that female U. lugens can recognize their host plants by detecting key host volatile compounds, using a set of ORNs tuned to host volatiles, and discriminate them from non-host plants using another set of ORNs specialized for non-host volatiles. The ORNs with broad response spectra may enhance the discrimination between host and non-host plants by adding moderately selective sensitivity. Based on our finding, it is suggested that phytophagous insects use the combinational input from both host-specific and non-host specific ORNs for locating their host plants, and the electrophysiological characterization of ORN profiles would be useful in predicting the range of host plants in phytophagous insects.

Implications of individual variation in insect behavior for host specificity testing in weed biocontrol

This study shows that individual behavioral variation is an under-recognised source of error that may affect the outcome of host range tests in a stenophagous species. Original specificity testing of the broom seed beetle, Bruchidius villosus (F.) (Coleoptera: Chrysomelidae: Bruchinae), a biocontrol agent for Scotch broom, Cytisus scoparius (L.) Link (Fabaceae: Genisteae), failed to detect its ability to oviposit in the field on a congeneric non-target plant, the exotic Cytisus proliferus L.f. (Fabaceae: Genisteae). These tests were repeated using individual beetles from the original UK collection sites and from New Zealand, 15 generations post release. In the original tests, low replication of small batches of females masked high levels of individual variation in oviposition preference. Although most beetles showed strong preference for the target weed, there was some indication that New Zealand beetles showed higher preference for the non-target than UK beetles.