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Cold tolerance of New Zealand alpine insects
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/cryo.1996.0064openalex-snapshot
Recrystallization in a Freezing Tolerant Antarctic Nematode,Panagrolaimus davidi,and an Alpine Weta,Hemideina maori(Orthoptera; Stenopelmatidae)
inferredcites →https://doi.org/10.1007/s00360-011-0561-7openalex-snapshot
Skin ice nucleators and glycerol in the freezing-tolerant frog Litoria ewingii
inferredcites →https://doi.org/10.1007/s003600050215openalex-snapshot
Microclimate and variations in haemolymph composition in the freezing-tolerant New Zealand alpine weta Hemideina maori Hutton (Orthoptera: Stenopelmatidae)
inferredcites →https://doi.org/10.1007/s00442-011-1983-3openalex-snapshot
Freeze fitness in alpine Tiger moth caterpillars and their parasitoids
inferredcites →https://doi.org/10.1016/0169-5347(93)90004-9openalex-snapshot
The New Zealand biota: Historical background and new research
inferredcites →https://doi.org/10.1016/0300-9629(78)90091-9openalex-snapshot
Haemolymph composition of two species of new zealand weta, Hemideina (orthoptera; stenopelmatidae)
inferredcites →https://doi.org/10.1016/0305-0491(95)00080-1openalex-snapshot
Hemolymph ice nucleating proteins from the New Zealand alpine weta Hemideina maori (Orthoptera: Stenopelmatidae)
inferredcites →https://doi.org/10.1016/0306-4565(92)90019-copenalex-snapshot
Freezing tolerance of the New Zealand alpine weta, Hemideina maori Hutton [Orthoptera; Stenopelmatidae]
inferredcites →https://doi.org/10.1016/j.cryobiol.2004.09.004openalex-snapshot
Freezing and cryoprotective dehydration in an Antarctic nematode (Panagrolaimus davidi) visualised using a freeze substitution technique
inferredcites →https://doi.org/10.1016/j.cryobiol.2005.07.001openalex-snapshot
Ice-active proteins from the Antarctic nematode Panagrolaimus davidi
inferredcites →https://doi.org/10.1016/j.jinsphys.2003.12.001openalex-snapshot
Intracellular freezing and survival in the freeze tolerant alpine cockroach Celatoblatta quinquemaculata
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.04.016openalex-snapshot
Cold hardiness of Apteropanorpa tasmanica Carpenter (Mecoptera: Apteropanorpidae)
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.09.007openalex-snapshot
Ice-active proteins and cryoprotectants from the New Zealand alpine cockroach, Celatoblatta quinquemaculata
inferredcites →https://doi.org/10.1016/j.jinsphys.2009.07.014openalex-snapshot
Cryoprotection in dampwood termites (Termopsidae, Isoptera)
inferredcites →https://doi.org/10.1016/j.jinsphys.2009.11.012openalex-snapshot
Cold tolerance of first-instar nymphs of the Australian plague locust, Chortoicetes terminifera
inferredcites →https://doi.org/10.1016/j.ympev.2009.07.007openalex-snapshot
Phylogeographic history of the New Zealand stick insect Niveaphasma annulata (Phasmatodea) estimated from mitochondrial and nuclear loci
inferredcites →https://doi.org/10.1016/s0022-1910(97)00018-8openalex-snapshot
Avoidance of intracellular freezing by the freezing-tolerant New Zealand Alpine weta Hemideina maori (Orthoptera: Stenopelmatidae)
inferredcites →https://doi.org/10.1016/s0022-1910(99)00193-6openalex-snapshot
Water relations of the freeze-tolerant New Zealand alpine cockroach Celatoblatta quinquemaculata (Dictyoptera: Blattidae)
inferredcites →https://doi.org/10.1016/s0169-5347(03)00014-4openalex-snapshot
Insects at low temperatures: an ecological perspective
inferredcites →https://doi.org/10.1017/cbo9780511675997openalex-snapshot
Low Temperature Biology of Insects
inferredcites →https://doi.org/10.1017/cbo9780511675997.002openalex-snapshot
A primer on insect cold-tolerance
inferredcites →https://doi.org/10.1017/s0031182000078409openalex-snapshot
Cold tolerance of an endoparasitic nematode within a freezing-tolerant orthopteran host
inferredcites →https://doi.org/10.1017/s1464793102006024openalex-snapshot
Climatic variability and the evolution of insect freeze tolerance
inferredcites →https://doi.org/10.1034/j.1600-0706.2001.930211.xopenalex-snapshot
Field ecology of freeze tolerance: interannual variation in cooling rates, freeze‐thaw and thermal stress in the microhabitat of the alpine cockroach Celatoblatta quinquemaculata
inferredcites →https://doi.org/10.1046/j.1365-2311.1997.00087.xopenalex-snapshot
Seasonal variation in freezing tolerance of the New Zealand alpine cockroach Celatoblatta quinquemaculata
inferredcites →https://doi.org/10.1046/j.1365-2435.2002.00634.xopenalex-snapshot
Metabolic cold adaptation in insects: a large‐scale perspective
inferredcites →https://doi.org/10.1046/j.1365-3032.1998.2310001.xopenalex-snapshot
Cold tolerance of a New Zealand alpine cockroach, Celatoblatta quinquemaculata (Dictyoptera, Blattidae)
inferredcites →https://doi.org/10.1046/j.1365-3032.1999.00112.xopenalex-snapshot
Ice nucleation and freezing tolerance in New Zealand alpine and lowland weta, Hemideina spp. (Orthoptera; Stenopelmatidae)
inferredcites →https://doi.org/10.1046/j.1439-0418.2002.00643.xopenalex-snapshot
The Biology of Wetas, King Crickets and their Allies
inferredcites →https://doi.org/10.1078/0031-4056-00073openalex-snapshot
Microhabitat selection and seasonality of alpine invertebrates
inferredcites →https://doi.org/10.1079/9780851994086.0035openalex-snapshot
Habitats and biogeography of New Zealand's deinacridine and tusked weta species.
inferredcites →https://doi.org/10.1080/0028825x.1970.10430156openalex-snapshot
The high‐alpine vegetation of Central Otago, New Zealand
inferredcites →https://doi.org/10.1111/j.1095-8312.2007.00807.xopenalex-snapshot
Evolutionary radiation of the cicada genus Maoricicada Dugdale (Hemiptera: Cicadoidea) and the origins of the New Zealand alpine biota
inferredcites →https://doi.org/10.1111/j.1365-2435.2005.00962.xopenalex-snapshot
Climatic variability and hemispheric differences in insect cold tolerance: support from southern Africa
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02160.xopenalex-snapshot
Adaptive radiation within New Zealand endemic species of the cockroach genus Celatoblatta Johns (Blattidae): a response to Plio‐Pleistocene mountain building and climate change
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04294.xopenalex-snapshot
New Zealand phylogeography: evolution on a small continent
inferredcites →https://doi.org/10.1111/j.1365-3032.2010.00731.xopenalex-snapshot
Tolerance of freezing in caterpillars of the New Zealand Magpie moth ( Nyctemera annulata )
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.00980.xopenalex-snapshot
ONSET OF GLACIATION DROVE SIMULTANEOUS VICARIANT ISOLATION OF ALPINE INSECTS IN NEW ZEALAND
inferredcites →https://doi.org/10.1146/annurev.physiol.63.1.327openalex-snapshot
Antifreeze and Ice Nucleator Proteins in Terrestrial Arthropods
inferredcites →https://doi.org/10.1152/physrev.1985.65.4.799openalex-snapshot
Physiology of cold tolerance in insects
inferredcites →https://doi.org/10.1152/physrev.1998.78.1.247openalex-snapshot
Functional Significance of Cell Volume Regulatory Mechanisms
inferredcites →https://doi.org/10.1242/jeb.201.14.2195openalex-snapshot
Cold Inhibition of Cell Volume Regulation During the Freezing of Insect Malpighian Tubules
inferredcites →https://doi.org/10.1242/jeb.201.2.227openalex-snapshot
Freezing Survival by Isolated Malpighian Tubules of the New Zealand Alpine Weta Hemideina Maori
inferredcites →https://doi.org/10.5860/choice.42-0935openalex-snapshot
The Natural history of southern New Zealand
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.2022.808.1721zenodo-depositor-declared
High alpine sorcerers: revision of the cave wētā genus Pharmacus Pictet & de Saussure (Orthoptera: Rhaphidophoridae: Macropathinae), with the description of six new species and three new subspecies
inferred← citeshttps://doi.org/10.1002/cphy.c130007openalex-snapshot
Molecular Biology of Freezing Tolerance
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2013.tb00524.xopenalex-snapshot
Molecular Biology of Freezing Tolerance
inferred← citeshttps://doi.org/10.1007/s00203-015-1094-3openalex-snapshot
Microbial community structure in the gut of the New Zealand insect Auckland tree weta (Hemideina thoracica)
inferred← citeshttps://doi.org/10.1007/s11829-024-10073-6openalex-snapshot
Environmental factors driving infestations of a keystone winter fruit by an invasive and a native fruit fly
inferred← citeshttps://doi.org/10.1007/s13355-016-0425-4openalex-snapshot
Intraspecific variation in heat tolerance of Drosophila prolongata (Diptera: Drosophilidae)
inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.11893-7openalex-snapshot
Cold Adaptations of Alpine Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-415819-1.00007-6openalex-snapshot
Circulatory Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-820359-0.00010-4openalex-snapshot
Circulatory systems
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00021-2openalex-snapshot
Insects in the cold
inferred← citeshttps://doi.org/10.1016/j.aspen.2025.102425openalex-snapshot
Functional complexity of Parthenium beetle, Zygogramma bicolorata (Pallister) under thermal-stress conditions: Insights from Gene Ontology
inferred← citeshttps://doi.org/10.1016/j.cbd.2012.10.005openalex-snapshot
Identification of cold-responsive genes in a New Zealand alpine stick insect using RNA-Seq
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.126802openalex-snapshot
Transcriptome sequencing reveals the effects of cadmium toxicity on the cold tolerance of the wolf spider Pirata subpiraticus
inferred← citeshttps://doi.org/10.1016/j.cris.2024.100092openalex-snapshot
Standard metabolic rate variation among New Zealand Orthoptera
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2015.07.008openalex-snapshot
Canalization of freeze tolerance in an alpine grasshopper
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.111034openalex-snapshot
Effects of long-term cadmium exposure on trehalose metabolism, growth, and development of Aedes albopictus (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1016/j.ibmb.2015.05.012openalex-snapshot
Shifts in metabolomic profiles of the parasitoid Nasonia vitripennis associated with elevated cold tolerance induced by the parasitoid's diapause, host diapause and host diet augmented with proline
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2014.08.005openalex-snapshot
Host diapause status and host diets augmented with cryoprotectants enhance cold hardiness in the parasitoid Nasonia vitripennis
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2015.02.012openalex-snapshot
Elevational variation in adult body size and growth rate but not in metabolic rate in the tree weta Hemideina crassidens
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2015.07.015openalex-snapshot
Cold tolerance of the montane Sierra leaf beetle, Chrysomela aeneicollis
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2014.07.007openalex-snapshot
Linking energetics and overwintering in temperate insects
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2018.03.018openalex-snapshot
Cold tolerance mechanisms of two arthropods from the Andean Range of Central Chile: Agathemera crassa (Insecta: Agathemeridae) and Euathlus condorito (Arachnida: Theraphosidae)
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2024.103862openalex-snapshot
Thermal tolerance does not explain the altitudinal segregation of lowland and alpine aquatic insects
inferred← citeshttps://doi.org/10.1021/ac301946wopenalex-snapshot
Direct Measurement of the Thermal Hysteresis of Antifreeze Proteins (AFPs) Using Sonocrystallization
inferred← citeshttps://doi.org/10.1038/s41598-020-68941-zopenalex-snapshot
Characterization of Gromphadorhina coquereliana hemolymph under cold stress
inferred← citeshttps://doi.org/10.1073/pnas.1316709110openalex-snapshot
Impact of trehalose transporter knockdown on Anopheles gambiae stress adaptation and susceptibility to Plasmodium falciparum infection
inferred← citeshttps://doi.org/10.1080/00779962.2013.784235openalex-snapshot
Overwintering in New Zealand stick insects
inferred← citeshttps://doi.org/10.1080/03036758.2022.2130367openalex-snapshot
Key questions on the evolution and biogeography of New Zealand alpine insects
inferred← citeshttps://doi.org/10.1080/21505594.2016.1199316openalex-snapshot
Trehalase plays a role in macrophage colonization and virulence ofBurkholderia pseudomalleiin insect and mammalian hosts
inferred← citeshttps://doi.org/10.1086/689481openalex-snapshot
Patterns and Processes in Nocturnal and Crepuscular Pollination Services
inferred← citeshttps://doi.org/10.1111/aen.12116openalex-snapshot
Evolution of N ew Z ealand insects: summary and prospectus for future research
inferred← citeshttps://doi.org/10.1111/een.13397openalex-snapshot
Winter fleshy‐fruited plants are the catalysts for spring populations of an invasive fruit fly
inferred← citeshttps://doi.org/10.1111/fwb.14190openalex-snapshot
Thermal biology of aquatic insects in alpine lakes: Insights from diving beetles
inferred← citeshttps://doi.org/10.1111/phen.12485openalex-snapshot
The physiological changes and the impact of rapid cold hardening on the survival ability of Dastarcus helophoroides (Fairmaire) (Coleoptera: Bothrideridae) under cold stress
inferred← citeshttps://doi.org/10.1146/annurev-ento-011613-162036openalex-snapshot
Physiology of Environmental Adaptations and Resource Acquisition in Cockroaches
inferred← citeshttps://doi.org/10.1152/japplphysiol.01117.2011openalex-snapshot
Comments on Point:Counterpoint: High altitude is/is not for the birds!
inferred← citeshttps://doi.org/10.1201/9781315373638-7openalex-snapshot
Physiological ecology and conservation of anuran amphibians
inferred← citeshttps://doi.org/10.1201/b20420-8openalex-snapshot
Assessing the physiological sensitivity of amphibians to extreme environmental change using the stress endocrine responses
inferred← citeshttps://doi.org/10.1242/jeb.213744openalex-snapshot
Thermal stress causes DNA damage and mortality in a tropical insect
inferred← citeshttps://doi.org/10.1657/aaar0015-064openalex-snapshot
Effects of Cushion Plants on High-Altitude Soil Microarthropod Communities: Cushions Increase Abundance and Diversity of Mites (Acari), but not Springtails (Collembola)
inferred← citeshttps://doi.org/10.20417/nzjecol.41.18openalex-snapshot
Impacts of introduced mammalian predators on New Zealand’s alpine fauna
inferred← citeshttps://doi.org/10.3389/fphys.2019.01623openalex-snapshot
TMT-Based Quantitative Proteomic Profiling of Overwintering Lissorhoptrus oryzophilus
inferred← citeshttps://doi.org/10.3390/insects13080753openalex-snapshot
Fruit Fly in a Challenging Environment: Impact of Short-Term Temperature Stress on the Survival, Development, Reproduction, and Trehalose Metabolism of Bactrocera dorsalis (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.3390/insects13100909openalex-snapshot
The Effect of Ice-Nucleation-Active Bacteria on Metabolic Regulation in Evergestis extimalis (Scopoli) (Lepidoptera: Pyralidae) Overwintering Larvae on the Qinghai-Tibet Plateau
inferred← citeshttps://doi.org/10.3390/insects14010089openalex-snapshot
Insect Freeze-Tolerance Downunder: The Microbial Connection
inferred← citeshttps://doi.org/10.3897/zookeys.707.12649openalex-snapshot
Austromonticola, a new genus of broad-nosed weevil (Coleoptera, Curculionidae, Entiminae) from montane areas of New Zealand
inferred← citeshttps://doi.org/10.5772/39027openalex-snapshot
Supercooling and Freezing Tolerant Animals
inferred← citeshttps://doi.org/10.7287/peerj.10864v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Expression analysis of genes related to cold tolerance in Dendroctonus valens (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.10864v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Expression analysis of genes related to cold tolerance in Dendroctonus valens (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.10864v0.3/reviews/2openalex-snapshot
Peer Review #2 of "Expression analysis of genes related to cold tolerance in Dendroctonus valens (v0.3)"
inferred← citeshttps://doi.org/10.7717/peerj.10864openalex-snapshot
Expression analysis of genes related to cold tolerance in Dendroctonus valens
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