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Positive and negative effects of phoretic mites on the reproductive output of an invasive bark beetle
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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/anbe.2002.3030openalex-snapshot
Host discrimination by two desert fleas using an odour cue
inferredcites →https://doi.org/10.1007/bf00052079openalex-snapshot
The potential role of phoresy in the evolution of parasitism: radiolabelling (tritium) evidence from an astigmatid mite
inferredcites →https://doi.org/10.1007/bf00171660openalex-snapshot
Tactics of parasitic American coots: host choice and the pattern of egg dispersion among host nests
inferredcites →https://doi.org/10.1007/bf00292505openalex-snapshot
The costs and benefits of cooperation between the Australian lycaenid butterfly, Jalmenus evagoras, and its attendant ants
inferredcites →https://doi.org/10.1007/s00442-005-0312-0openalex-snapshot
Antagonisms, mutualisms and commensalisms affect outbreak dynamics of the southern pine beetle
inferredcites →https://doi.org/10.1007/s004420050532openalex-snapshot
Host choice in the phoretic mite Parasitellus fucorum (Mesostigmata: Parasitidae): which bumblebee caste is the best?
inferredcites →https://doi.org/10.1007/s10493-007-9105-yopenalex-snapshot
Predation of entomopathogenic nematodes by Sancassania sp. (Acari: Acaridae)
inferredcites →https://doi.org/10.1016/0169-4758(93)90153-7openalex-snapshot
Ectoparasites: Direct impact on host fitness
inferredcites →https://doi.org/10.1016/j.foreco.2008.02.037openalex-snapshot
Factors influencing pine engraver (Ips pini Say) colonization of ponderosa pine (Pinus ponderosa Dougl. ex. Laws.) slash in Northern Arizona
inferredcites →https://doi.org/10.1016/s0169-5347(00)01924-8openalex-snapshot
Mites and birds: diversity, parasitism and coevolution
inferredcites →https://doi.org/10.1017/s0031182004005232openalex-snapshot
Size versus health as a cue for host choice: a test of the tasty chick hypothesis
inferredcites →https://doi.org/10.1034/j.1600-0706.2003.12599.xopenalex-snapshot
Strong indirect interactions of Tarsonemus mites (Acarina: Tarsonemidae) and Dendroctonus frontalis (Coleoptera: Scolytidae)
inferredcites →https://doi.org/10.1038/nature06777openalex-snapshot
Mountain pine beetle and forest carbon feedback to climate change
inferredcites →https://doi.org/10.1046/j.1440-6055.2000.0152b.xopenalex-snapshot
Mites: Ecology, Evolution and Behaviour.
inferredcites →https://doi.org/10.1080/00049158.1967.10675435openalex-snapshot
Ips grandicollis in South Australia
inferredcites →https://doi.org/10.1080/08927014.2006.9522710openalex-snapshot
You are looking mitey fine: parasites as direct indicators of fitness in the mating system of a host species
inferredcites →https://doi.org/10.1086/282929openalex-snapshot
The Optimal Balance between Size and Number of Offspring
inferredcites →https://doi.org/10.1093/ee/37.4.956openalex-snapshot
Multipartite Symbioses Among Fungi, Mites, Nematodes, and the Spruce Beetle,Dendroctonus rufipennis
inferredcites →https://doi.org/10.1111/j.0021-8790.2004.00799.xopenalex-snapshot
Life history and fitness consequences of ectoparasites
inferredcites →https://doi.org/10.1111/j.1096-3642.1983.tb00858.xopenalex-snapshot
The evolution of mating systems in bark and ambrosia beetles (Coleoptera: Scolytidae and Platypodidae)
inferredcites →https://doi.org/10.1111/j.1365-2311.2009.01103.xopenalex-snapshot
Harem size and oviposition behaviour in a polygynous bark beetle
inferredcites →https://doi.org/10.1111/j.1439-0418.1977.tb04273.xopenalex-snapshot
The life cycle and behaviour of Macrocheles boudreauxi Krantz12
inferredcites →https://doi.org/10.1111/j.1440-6055.1991.tb02187.xopenalex-snapshot
EFFECT OF SIX CHEMICALS ON THE INSECTS, MITES, NEMATODES AND FUNGI ASSOCIATED WITH IPS GRANDICOLLIS (EICHHOFF) (COLEOPTERA: SCOLYTIDAE) IN NORTHEASTERN NEW SOUTH WALES
inferredcites →https://doi.org/10.1111/j.1461-9555.2005.00261.xopenalex-snapshot
Phoretic mites and nematode associates of Scolytus multistriatus and Scolytus pygmaeus (Coleoptera: Scolytidae) in Austria
inferredcites →https://doi.org/10.1111/j.1469-185x.1982.tb00374.xopenalex-snapshot
PHORESY AS MIGRATION ‐ SOME FUNCTIONAL ASPECTS OF PHORESY IN MITES
inferredcites →https://doi.org/10.1111/j.1469-7998.1994.tb06070.xopenalex-snapshot
Observations on a mite (Poecilochirus davydovae) predatory on the eggs of burying beetles (Nicrophorus vespilloides) with a review of its taxonomic status
inferredcites →https://doi.org/10.1139/z06-110openalex-snapshot
Feather mites are positively associated with daily survival in cliff swallows
inferredcites →https://doi.org/10.1139/z08-022openalex-snapshot
Life cycle and sexual mode adaptations of the parasitic mite Ensliniella parasitica (Acari: Winterschmidtiidae) to its host, the eumenine wasp Allodynerus delphinalis (Hymenoptera: Vespidae)
inferredcites →https://doi.org/10.1146/annurev.ento.42.1.179openalex-snapshot
Interactions among Scolytid bark beetles, their associated fungi, and live host conifers.
inferredcites →https://doi.org/10.1146/annurev.ento.47.091201.145257openalex-snapshot
The Ecology and Evolution of Ant Association in the Lycaenidae (Lepidoptera)
inferredcites →https://doi.org/10.1603/0013-8746(2006)099[0189:ecofaw]2.0.co;2openalex-snapshot
Ergosterol Content of Fungi Associated with Dendroctonus ponderosae and Dendroctonus rufipennis (Coleoptera: Curculionidae, Scolytinae)
inferredcites →https://doi.org/10.1603/0013-8746(2008)101[266:pmdamb]2.0.co;2openalex-snapshot
Phoretic Mite Discrimination Among Male Burying Beetle (Nicrophorus investigator) Hosts
inferredcites →https://doi.org/10.1603/0046-225x(2008)37[956:msafmn]2.0.co;2openalex-snapshot
Multipartite Symbioses Among Fungi, Mites, Nematodes, and the Spruce Beetle, Dendroctonus rufipennis
inferredcites →https://doi.org/10.2307/1938645openalex-snapshot
Effects of Parasitism by a Haematophagous Mite on Reproduction in the Barn Swallow
inferredcites →https://doi.org/10.2307/2390508openalex-snapshot
Effect of Vertically Transmitted Ectoparasites on the Reproductive Success of Swifts (Apus apus)
inferredcites →https://doi.org/10.2307/3545356openalex-snapshot
Parasitism and Host Reproductive Effort
inferredcites →https://doi.org/10.2307/3545585openalex-snapshot
Estimating Fitness: A Comparison of Body Condition Indices
inferredcites →https://doi.org/10.4039/ent101862-8openalex-snapshot
SECONDARY SEXUAL CHARACTERS IN THE NORTH AMERICAN SPECIES OF THE GENUS IPS (COLEOPTERA: SCOLYTIDAE)
inferredcites →https://doi.org/10.4039/entm10160fvopenalex-snapshot
REVIEW OF HOLARCTIC TARSONEMID MITES (ACARINA: PROSTIGMATA) PARASITIZING EGGS OF IPINE BARK BEETLES
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2021.04.009zenodo-depositor-declared
Ectoparasites of hedgehogs: From flea mite phoresy to their role as vectors of pathogens
inferred← citeshttps://doi.org/10.24349/upy5-taezzenodo-depositor-declared
Phoretic mite assemblage of the pinyon pine beetle, Ips confusus (Curculionidae: Scolytinae), in Arizona
inferred← citeshttps://doi.org/10.1002/ece3.10338openalex-snapshot
Body size‐dependent effects on the distribution patterns of phoretic mite species assemblages on Rhynchophorus ferrugineus (Olivier, 1790)
inferred← citeshttps://doi.org/10.1002/ece3.4570openalex-snapshot
Fitness costs of phoretic nematodes in the burying beetle, Nicrophorus vespilloides
inferred← citeshttps://doi.org/10.1002/ece3.71733openalex-snapshot
No Evidence That the Phoretic Mite Poecilochirus carabi Influences Mate Choice or Fitness in the Host Burying Beetle Nicrophorus nepalensis
inferred← citeshttps://doi.org/10.1002/ecm.1331openalex-snapshot
Necrobiome framework for bridging decomposition ecology of autotrophically and heterotrophically derived organic matter
inferred← citeshttps://doi.org/10.1007/978-94-007-7164-2_4openalex-snapshot
Life Cycles, Development and Size
inferred← citeshttps://doi.org/10.1016/b978-0-12-822145-7.00007-6openalex-snapshot
Effects of rising temperatures on ectosymbiotic communities associated with bark and ambrosia beetles
inferred← citeshttps://doi.org/10.1016/j.asd.2012.02.006openalex-snapshot
Anatomy and fine structure of pedicellar glands in phoretic deutonymphs of uropodid mites (Acari: Mesostigmata)
inferred← citeshttps://doi.org/10.1080/01647954.2019.1656286openalex-snapshot
Relationships between phoretic mites and their carrier, the banana pseudostem weevil Odoiporus longicollis Oliver (Coleoptera: Curculionidae)
inferred← citeshttps://doi.org/10.1101/2023.02.06.527267openalex-snapshot
Body size-dependent effects on the distribution patterns of phoretic mites of the multi-symbiont Rhynchophorus ferrugineus (Olivier, 1790) host
inferred← citeshttps://doi.org/10.1111/1365-2435.13451openalex-snapshot
Density‐dependent fitness effects stabilize parasitic hitchhiking within a mutualism
inferred← citeshttps://doi.org/10.1111/aen.12077openalex-snapshot
Biology of the bark beetle I ps grandicollis E ichhoff ( C oleoptera: S colytinae) and its arthropod, nematode and microbial associates: a review of management opportunities for A ustralia
inferred← citeshttps://doi.org/10.1111/brv.12654openalex-snapshot
Phoresy in animals: review and synthesis of a common but understudied mode of dispersal
inferred← citeshttps://doi.org/10.3390/ijms25094906openalex-snapshot
Physiological Measurements and Transcriptomics Reveal the Fitness Costs of Monochamus saltuarius to Bursaphelenchus xylophilus
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