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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

https://doi.org/10.1111/aen.12121
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9780470696200.ch7openalex-snapshot
Food‐Searching in Parasitoids: The Dilemma of Choosing between ‘Immediate’ or Future Fitness Gains
inferredcites →https://doi.org/10.1002/arch.940130103openalex-snapshot
How parasitoids deal with the immune system of their host: An overview
inferredcites →https://doi.org/10.1007/978-1-4020-4401-4_1openalex-snapshot
CONCEPTS AND VISIONS OF BIOLOGICAL CONTROL
inferredcites →https://doi.org/10.1007/978-1-4615-1765-8_3openalex-snapshot
Parasitoid Foraging and Learning
inferredcites →https://doi.org/10.1007/978-1-4615-2814-2_3openalex-snapshot
Learning of Host-Finding Cues by Hymenopterous Parasitoids
inferredcites →https://doi.org/10.1007/978-1-4615-7299-2_6openalex-snapshot
Insect Host Responses Against Parasitoids and the Parasitoid’s Resistance: With Emphasis on the Lepidoptera-Hymenoptera Association
inferredcites →https://doi.org/10.1007/bf01012345openalex-snapshot
Beneficial arthropod behavior mediated by airborne semiochemicals
inferredcites →https://doi.org/10.1007/bf01053293openalex-snapshot
Beneficial arthropod behavior mediated by airborne semiochemicals. VIII. Learning of host-related odors induced by a brief contact experience with host by-products inCotesia marginiventris (Cresson), a generalist larval parasitoid
inferredcites →https://doi.org/10.1007/bf01065962openalex-snapshot
Influence of host behavior and host size on the success of oviposition ofCotesia urabae andDolichogenidea eucalypti (Hymenoptera: Braconidae)
inferredcites →https://doi.org/10.1007/bf02373121openalex-snapshot
Host specificity testing and suitability of the parasitoidMicroctonus hyperodae (Hym.: Braconidae, Euphorinae) as a biological control agent ofListronotus bonariensis (Col.: Curculionidae) in New Zealand
inferredcites →https://doi.org/10.1007/s10526-005-3633-3openalex-snapshot
Methods Used to Assess Non-target Effects of Invertebrate Biological Control Agents of Arthropod Pests
inferredcites →https://doi.org/10.1007/s10526-013-9524-0openalex-snapshot
Phenology, synchrony and host range of the Tasmanian population of Cotesia urabae introduced into New Zealand for the biocontrol of Uraba lugens
inferredcites →https://doi.org/10.1016/0006-3207(96)00027-4openalex-snapshot
Risks of species introduced for biological control
inferredcites →https://doi.org/10.1016/b978-0-12-045580-5.50008-2openalex-snapshot
Individual Variation in Host Location by Phytophagous Insects
inferredcites →https://doi.org/10.1016/b978-012257305-7/50069-2openalex-snapshot
Nutrition of Entomophagous Insects and Other Arthropods
inferredcites →https://doi.org/10.1016/j.biocontrol.2005.01.013openalex-snapshot
Effects of host deprivation and egg expenditure on the reproductive capacity of Mastrus ridibundus, an introduced parasitoid for the biological control of codling moth in California
inferredcites →https://doi.org/10.1016/s1049-9644(02)00121-4openalex-snapshot
Non-target host acceptance and parasitism by Trichogramma brassicae Bezdenko (Hymenoptera: Trichogrammatidae) in the laboratory
inferredcites →https://doi.org/10.1016/s1049-9644(03)00059-8openalex-snapshot
Laboratory and field host preferences of introduced Cotesia spp. parasitoids (Hymenoptera: Braconidae) between native and invasive Pieris butterflies
inferredcites →https://doi.org/10.1017/cbo9780511661730.007openalex-snapshot
Benefits and Risks of Classical Biological Control
inferredcites →https://doi.org/10.1017/cbo9780511806384openalex-snapshot
Experimental Design and Data Analysis for Biologists
inferredcites →https://doi.org/10.1023/a:1007404710817openalex-snapshot
Should arthropod parasitoids and predators be subject to host range testing when used as biological control agents?
inferredcites →https://doi.org/10.1023/a:1021262931608openalex-snapshot
Environmental risk assessment of exotic natural enemies used in inundative biological control
inferredcites →https://doi.org/10.1046/j.1420-9101.1989.2030157.xopenalex-snapshot
An evolutionary interpretation of the “motivation to oviposit”
inferredcites →https://doi.org/10.1046/j.1570-7458.2002.01034.xopenalex-snapshot
Superparasitism in the solitary ectoparasitoid Aptesis nigrocincta: the influence of egg load and host encounter rate
inferredcites →https://doi.org/10.1071/zo9900347openalex-snapshot
The Phenologies of Cotesia-Urabae, Dolichogenidea-Eucalypti (Hymenoptera, Braconidae) and Their Host Uraba-Lugens (Lepidoptera, Noctuidae) in the Adelaide Region
inferredcites →https://doi.org/10.1080/00779962.2012.724929openalex-snapshot
Laboratory rearing ofCotesia urabaeAustin and Allen (Hymenoptera: Braconidae), a biological control agent ofUraba lugensWalker (Lepidoptera: Nolidae)
inferredcites →https://doi.org/10.1080/00779962.2012.744908openalex-snapshot
First releases and monitoring of the biological control agentCotesia urabaeAustin and Allen (Hymenoptera: Braconidae)
inferredcites →https://doi.org/10.1080/0958315021000039860openalex-snapshot
Time-dependent Changes in the Host-acceptance Threshold of Insects: Implications for Host Specificity Testing of Candidate Biological Control Agents
inferredcites →https://doi.org/10.1093/ee/20.2.458openalex-snapshot
Uraba lugens (Lepidoptera: Noctuidae) and Its Parasitoids (Hymenoptera: Braconidae): Temperature, Host Size, and Development
inferredcites →https://doi.org/10.1093/ee/21.4.760openalex-snapshot
Host Switching in Brachymeria intermedia (Hymenoptera: Chalcididae), a Pupal Endoparasitoid of Lymantria dispar (Lepidoptera: Lymantriidae)
inferredcites →https://doi.org/10.1093/ee/26.3.694openalex-snapshot
Laboratory Nontarget Host Range of the Introduced Parasitoids Microctonus aethiopoides and M. hyperodae (Hymenoptera: Braconidae) Compared with Field Parasitism in New Zealand
inferredcites →https://doi.org/10.1111/j.1365-2664.2007.01331.xopenalex-snapshot
Using a pheromone lure survey to establish the native and potential distribution of an invasive Lepidopteran, Uraba lugens
inferredcites →https://doi.org/10.1111/j.1365-3032.1992.tb01016.xopenalex-snapshot
Effect of host diet and preflight experience on the flight responses of Microplitis croceipes (Cresson)
inferredcites →https://doi.org/10.1111/j.1365-3032.2003.00341.xopenalex-snapshot
Effect of biotic and abiotic factors on reproductive parameters of the synovigenic endoparasitoid Venturia canescens
inferredcites →https://doi.org/10.1111/j.1440-6055.1990.tb00367.xopenalex-snapshot
URABA LUGENS WALKER (LEPIDOPTERA: NOCTUIDAE): LARVAL SURVIVAL AND PARASITOID BIOLOGY IN THE FIELD IN SOUTH AUSTRALIA
inferredcites →https://doi.org/10.1111/j.1440-6055.2010.00760.xopenalex-snapshot
Biology and pest status of Uraba lugens Walker (Lepidoptera: Nolidae) in Australia and New Zealand
inferredcites →https://doi.org/10.1111/j.1570-7458.1992.tb01601.xopenalex-snapshot
Comparison of learning in related generalist and specialist eucoilid parasitoids
inferredcites →https://doi.org/10.1111/jen.12062openalex-snapshot
Pre‐release risk assessment of the egg‐parasitoid G ryon pennsylvanicum for classical biological control of L eptoglossus occidentalis
inferredcites →https://doi.org/10.1139/x02-208openalex-snapshot
Spatial pattern of invading Dendroctonus micans (Coleoptera: Scolytidae) populations in the United Kingdom
inferredcites →https://doi.org/10.1146/annurev.en.21.010176.001545openalex-snapshot
Biotic Interference with Insects Imported for Weed Control
inferredcites →https://doi.org/10.1146/annurev.en.36.010191.002413openalex-snapshot
Environmental Impacts of Classical Biological Control
inferredcites →https://doi.org/10.1146/annurev.en.38.010193.001343openalex-snapshot
Insect Behavioral and Morphological Defenses Against Parasitoids
inferredcites →https://doi.org/10.1146/annurev.ento.48.060402.102800openalex-snapshot
N ONTARGET E FFECTS —T HE A CHILLES ' H EEL OF B IOLOGICAL C ONTROL ? Retrospective Analyses to Reduce Risk Associated with Biocontrol Introductions
inferredcites →https://doi.org/10.1146/annurev.ento.51.110104.151129openalex-snapshot
ASSESSING RISKS OF RELEASING EXOTIC BIOLOGICAL CONTROL AGENTS OF ARTHROPOD PESTS
inferredcites →https://doi.org/10.1163/002829679x00412openalex-snapshot
Discrimination Between Parasitized and Unparasitized Hosts in the Egg Parasite Trichogramma Embryophagum (Hym.: Trichogrammatidae): a Matter of Learning and Forgetting
inferredcites →https://doi.org/10.1603/ec13318openalex-snapshot
Host Range Testing of Tamarixia radiata (Hymenoptera: Eulophidae) Sourced From the Punjab of Pakistan for Classical Biological Control of Diaphorina citri (Hemiptera: Liviidae: Euphyllurinae: Diaphorinini) in California
inferredcites →https://doi.org/10.1890/1051-0761(2000)010[0689:bicegc]2.0.co;2openalex-snapshot
BIOTIC INVASIONS: CAUSES, EPIDEMIOLOGY, GLOBAL CONSEQUENCES, AND CONTROL
inferredcites →https://doi.org/10.2134/jeq1998.00472425002700010038xopenalex-snapshot
Experiments in Ecology: Their Logical Design and Interpretation Using Analysis of Variance
inferredcites →https://doi.org/10.2307/1312873openalex-snapshot
Host Specificity and Biological Pest Control
inferredcites →https://doi.org/10.2307/3544896openalex-snapshot
Egg Load as a Major Source of Variability in Insect Foraging and Oviposition Behavior
inferredcites →https://doi.org/10.2307/3565872openalex-snapshot
A General Model for Individual Host Selection
inferredcites →https://doi.org/10.2307/5419openalex-snapshot
Foraging and Oviposition Decisions in the Parasitoid Aphytis lingnanensis: Distinguishing the Influences of Egg Load and Experience
inferredcites →https://doi.org/10.30843/nzpp.2007.60.4604openalex-snapshot
A method for host range testing of a biological control agent for Uraba lugens
inferredcites →https://doi.org/10.30843/nzpp.2009.62.4773openalex-snapshot
Nontarget species selection for host range testing of Cotesia urabae

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.5852/ejt.2020.667zenodo-depositor-declared
Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
inferred← citeshttps://doi.org/10.1007/s10526-016-9716-5openalex-snapshot
Laboratory odour-specificity testing of Cotesia urabae to assess potential risks to non-target species
inferred← citeshttps://doi.org/10.1007/s10526-016-9770-zopenalex-snapshot
A comparison of methods for selecting non-target species for risk assessment of the biological control agent Cotesia urabae
inferred← citeshttps://doi.org/10.1007/s10526-023-10181-xopenalex-snapshot
Characterising uncertainty in risk assessments for biological control: using case studies from New Zealand to inform future research
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2016.08.008openalex-snapshot
Retrospective risk assessment reveals likelihood of potential non-target attack and parasitism by Cotesia urabae (Hymenoptera: Braconidae): A comparison between laboratory and field-cage testing results
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2022.105136openalex-snapshot
Field assessment of parasitism on the New Zealand endemic Nyctemera annulata by Cotesia urabae: Can non-target impacts be ruled out?
inferred← citeshttps://doi.org/10.1017/s0007485316001127openalex-snapshot
Courtship and mating behaviour in the parasitoid wasp Cotesia urabae (Hymenoptera: Braconidae): mate location and the influence of competition and body size on male mating success
inferred← citeshttps://doi.org/10.1080/00779962.2025.2585532openalex-snapshot
A checklist and synopsis of Braconidae (Hymenoptera) in New Zealand
inferred← citeshttps://doi.org/10.1111/eea.12393openalex-snapshot
Olfactory cues used in host‐habitat location and host location by the parasitoid C otesia urabae
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