Host testing of the parasitoid Cotesia urabae (Austin & Allen, 1989) (Hymenoptera: Braconidae) to assess the risk posed to the New Zealand nolid moth Celama parvitis (Howes, 1917) (Lepidoptera: Nolidae): do host deprivation and experience influence accept

The electrical penetration graph (EPG) technique is being developed for rapid assessment of host range of potential xylem feeding invaders in New Zealand Stylet penetration behaviours of adult spittle bug Carystoterpa fingens were monitored for 12 h on grape lemon apple and kiwifruit plants using EPG A multiplechoice test of all four plant species was conducted concurrently with the EPG tests for comparison In EPG tests the longest probing and ingestion periods were recorded on grape and lemon while the shortest probing and ingestion periods were recorded on apple Results for kiwifruit were intermediate and not significantly different from the other plant types In the multiplechoice tests more insects were found on grape and lemon than on apple and kiwifruit The similar ranking of the host plants in both multiplechoice and EPG tests suggests that EPG is a valid tool for rapidly assessing host feeding acceptance and preference

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Retrospective host specificity testing of Cotesia urabae to assess the risk posed to the New Zealand nolid moth Celama parvitis

New Zealand Plant Protection ◽

10.30843/nzpp.2014.67.5772 ◽

2014 ◽

Vol 67 ◽

pp. 328-328

Author(s):

G.A. Avila ◽

T.M. Withers ◽

G.I. Holwell

Keyword(s):

Biological Control ◽

New Zealand ◽

Host Specificity ◽

Potential Risk ◽

Biological Control Agent ◽

Control Agent ◽

Laboratory Rearing ◽

Host Deprivation ◽

Retrospective Testing ◽

Host Specificity Testing

Additional retrospective testing of the gum leaf skeletoniser (Uraba lugens) biological control agent Cotesia urabae was conducted against the endemic moth Celama parvitis Although this native was included in host specificity testing before EPA approved the parasitoids release this work aimed to increase the sample size to better assess the potential risk posed The effect that different periods of host deprivation and prior oviposition experience had on the parasitoids readiness to attack was examined in a sequence of nochoice tests No parasitoids emerged from the 52 of larvae that survived to pupation thus confirming C parvitis as a nonhost Dissections of larvae that died during laboratory rearing revealed that 63 had contained a parasitoid but no C urabae parasitoid larvae developed beyond the second instar Significant differences were found in the attack times according to the parasitoids deprivation levels (age) and it was also observed that the duration until first attack significantly decreased after each nontarget presentation

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Magellanic Cloud Eclipsing Binaries: Primary Distance Indicators

Symposium - International Astronomical Union ◽

10.1017/s007418090011900x ◽

1999 ◽

Vol 190 ◽

pp. 563-566

Author(s):

J. D. Pritchard ◽

W. Tobin ◽

J. V. Clausen ◽

E. F. Guinan ◽

E. L. Fitzpatrick ◽

...

Keyword(s):

New Zealand ◽

Magellanic Cloud ◽

Eclipsing Binaries ◽

Fundamental Parameters ◽

Distance Indicators

Our collaboration involves groups in Denmark, the U.S.A. Spain and of course New Zealand. Combining ground-based and satellite (IUEandHST) observations we aim to determine accurate and precise stellar fundamental parameters for the components of Magellanic Cloud Eclipsing Binaries as well as the distances to these systems and hence the parent galaxies themselves. This poster presents our latest progress.

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Heat-Etching with a Bullivant Type II Simple Freeze-Cleave Device

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100067522 ◽

1970 ◽

Vol 28 ◽

pp. 106-107 ◽

Cited By ~ 1

Author(s):

Ronald S. Weinstein ◽

N. Scott McNutt

Keyword(s):

New Zealand ◽

General Hospital ◽

Massachusetts General Hospital ◽

Type I ◽

Type Ii ◽

Collaborative Effort ◽

Temperature And Pressure ◽

The University

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.

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A Cytochemical Study of Glucose-6-Phosphatase (G-6-PASE) in Cells Participating in Atherogenesis of Rabbit Aorta

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100115924 ◽

1975 ◽

Vol 33 ◽

pp. 460-461

Author(s):

Sidney D. Kobernick ◽

Edna A. Elfont ◽

Neddra L. Brooks

Keyword(s):

Lipid Metabolism ◽

New Zealand ◽

Aortic Wall ◽

Rabbit Aorta ◽

Plaque Formation ◽

Metabolic Changes ◽

Atherosclerotic Plaques ◽

Cytochemical Study ◽

Cellular Alteration ◽

New Zealand White Rabbits

This cytochemical study was designed to investigate early metabolic changes in the aortic wall that might lead to or accompany development of atherosclerotic plaques in rabbits. The hypothesis that the primary cellular alteration leading to plaque formation might be due to changes in either carbohydrate or lipid metabolism led to histochemical studies that showed elevation of G-6-Pase in atherosclerotic plaques of rabbit aorta. This observation initiated the present investigation to determine how early in plaque formation and in which cells this change could be observed.Male New Zealand white rabbits of approximately 2000 kg consumed normal diets or diets containing 0.25 or 1.0 gm of cholesterol per day for 10, 50 and 90 days. Aortas were injected jin situ with glutaraldehyde fixative and dissected out. The plaques were identified, isolated, minced and fixed for not more than 10 minutes. Incubation and postfixation proceeded as described by Leskes and co-workers.

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