about
Mitonuclear interactions, mtDNA-mediated thermal plasticity, and implications for the Trojan Female Technique for pest controlThe Trojan female technique: a novel, effective and humane approach for pest population controlPredicted responses of invasive mammal communities to climate-related changes in mast frequency in forest ecosystems.Climate warming may cause a parasite-induced collapse in coastal amphipod populations.Hybridization increases measures of innate and cell-mediated immunity in an endangered bird species.Introduced brown trout alter native acanthocephalan infections in native fish.Trematode infection causes malformations and population effects in a declining New Zealand fish.Discovery of novel virus sequences in an isolated and threatened bat species, the New Zealand lesser short-tailed bat (Mystacina tuberculata)The Trojan Female Technique for pest control: a candidate mitochondrial mutation confers low male fertility across diverse nuclear backgrounds in Drosophila melanogaster.The role of multiple wildlife hosts in the persistence and spread of bovine tuberculosis in New Zealand.Sex difference in the survival rate of wild brushtail possums (Trichosurus vulpecula) experimentally challenged with bovine tuberculosis.Relative competence of native and exotic fish hosts for two generalist native trematodes.Surveillance for arboviral zoonoses in New Zealand birds.Parasite spillback: a neglected concept in invasion ecology?New alphacoronavirus in Mystacina tuberculata bats, New ZealandWildlife diseases: from individuals to ecosystems.Emerging infectious diseases of wildlife: a critical perspective.Discovery and complete genome sequence of a novel circovirus-like virus in the endangered rowi kiwi, Apteryx rowi.Exploring the potential for Ross River virus emergence in New Zealand.Seroprevalence of antibodies to Rickettsia typhi in the Waikato region of New Zealand.Piroplasms of New Zealand seabirds.Exudative cloacitis in the kakapo (Strigops habroptilus) potentially linked to Escherichia coli infection.Rickettsia felis infections, New Zealand.Differential impact of a shared nematode parasite on two gamebird hosts: implications for apparent competition.Parasite-mediated competition between pheasant and grey partridge: a preliminary investigation.Parasites lost - do invaders miss the boat or drown on arrival?Patterns of parasite aggregation in the wild European rabbit (Oryctolagus cuniculus).Sustained protection against tuberculosis conferred to a wildlife host by single dose oral vaccination.Percutaneous interdigital injection of Mycobacterium bovis as a model for tuberculous lesion development in wild brushtail possums (Trichosurus vulpecula).A novel poxvirus lethal to red squirrels (Sciurus vulgaris).The role of shared parasites in the exclusion of wildlife hosts: Heterakis gallinarum in the ring-necked pheasant and the grey partridge.Wildlife disease ecology: from theory to policy.Unexpected consequences of vertebrate pest control: predictions from a four-species community model.Comparative effects of mites and lice on the reproductive success of rock doves (Columba livia).Ectoparasite virulence is linked to mode of transmission.Reciprocal Natural Selection on Host-Parasite Phenotypes.Do different parasite species interact in their effects on host fitness? A case study on parasites of the amphipod Paracalliope fluviatilisFirst direct estimate of the detection probability of bovine tuberculosis in possums by possum transmissionPododermatitis in Captive-Reared Black Stilts (Himantopus novaezelandiae)Oral vaccination reduces the incidence of tuberculosis in free-living brushtail possums
P50
Q26700025-B1B7BEF8-85F3-46F6-A3DA-F7CD71FDB88BQ28661634-FD30563F-EA5C-4536-B92A-9CC794BBAE3FQ30662888-2A1F664D-AAD7-4ED3-91D1-95DEB4C26C1BQ31002355-E34B9496-1A6E-492B-A4E5-607FA6249170Q33241057-8D56408B-0274-48D9-A32A-DA78B9DFDC61Q33852521-76C52939-83F0-4A5D-B2D8-B034B50A74E0Q35011087-54CF6234-EA02-43F2-9DE8-4FC95102D2CBQ35611071-043D1FB4-65E0-433C-8E1C-0F3BD2058906Q35818359-C67F34EB-DD35-4164-8044-43D8D60424E9Q36051365-233CA048-7FDE-474E-9750-87F6B4307ACDQ36090505-2DD6D7A7-4F4A-4674-82AE-194C1FC0A5E6Q37390780-46A0FB24-2CB6-4DB5-9295-58D55A292809Q37517981-4D0D6C06-6EF6-486A-B8E2-127F3FD32557Q37594021-FF1AF4D7-CF72-4ACE-950E-4C988872EE06Q37664573-EF36B0DB-F419-4978-AE16-176C43C834D3Q37782152-9BC44C0C-992C-44E4-9B3E-E3B4217DA9C3Q38364661-68529CEC-9A43-4833-9167-43D5D67EEBD8Q39821197-6B5755BD-B595-466B-8A86-4C8C63286859Q40171236-0FC5A0F0-EC63-46F3-B462-5B29ECCDF5E2Q40730304-49D79977-616B-4C0B-8682-DC190A3D5E73Q41746000-35CFE26C-AA16-444E-A9F5-C3CDFC54702FQ41755426-10D8A243-C8B1-4761-A3BC-B065785A889EQ42573362-3FA31329-C5A5-48AA-9F8B-B641C5010EE0Q42645942-49DC6390-3AF1-4630-B0DE-42DAE5170156Q42652526-9D851189-5AED-450C-ACE5-9CCED8A54D63Q44380813-1AD63A36-9169-48EC-B59C-436CA27C39A5Q44483608-3AE15BC2-B39C-4CF2-BD80-6E832A7C08EEQ44921185-68910731-4B02-4945-A704-E3C2C7A594B7Q45831525-1D42D527-2DE0-4277-A8E6-CA97DDA671FAQ47350683-69A4365D-F72C-404F-8BEF-EFBEDB0DD2A9Q50125219-BA25123D-8294-426C-973D-C184CC2B7165Q51205885-6FBC333D-4F19-4F01-A3B2-EFDE745A491CQ51724632-A566DA66-DE39-400D-90BE-43E226797A7AQ52540943-9344DC1D-9CEF-4F13-B6D4-F5C210394A95Q52542575-F510EF81-7312-4B13-AA47-8E093C3320C6Q52573387-07E5FA4E-51C0-4792-B6AC-F08BA4F3F7C7Q56953067-98E6D377-BEA4-43D4-95CC-A73603AD9228Q58433047-E818EFF7-8459-4326-B7F7-0F171F1154C5Q58433098-47DD09C5-1A44-4871-8ABA-EA1E97571126Q58433112-306F60ED-333D-45A2-A5D5-0A59D488C86C
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Daniel Tompkins
@ast
Daniel Tompkins
@en
Daniel Tompkins
@es
Daniel Tompkins
@fr
Daniel Tompkins
@nl
Daniel Tompkins
@sl
type
label
Daniel Tompkins
@ast
Daniel Tompkins
@en
Daniel Tompkins
@es
Daniel Tompkins
@fr
Daniel Tompkins
@nl
Daniel Tompkins
@sl
prefLabel
Daniel Tompkins
@ast
Daniel Tompkins
@en
Daniel Tompkins
@es
Daniel Tompkins
@fr
Daniel Tompkins
@nl
Daniel Tompkins
@sl
P106
P1153
7006431654
P21
P31
P496
0000-0003-3209-8084