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Predicting shifts in parasite distribution with climate change: a multitrophic level approach

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What this work says

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

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Global Climate Change and Emerging Infectious Diseases

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The consequences of urban land transformation on net primary productivity in the United States

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Climate Change and Vector-Borne Diseases

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Predicting species distribution and abundance responses to climate change: why it is essential to include biotic interactions across trophic levels

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Modeling of species distributions with Maxent: new extensions and a comprehensive evaluation

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Habitat shifts of endangered species under altered climate conditions: importance of biotic interactions

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Outbreaks of Clinical Cerebrospinal Elaphostrongylosis in Reindeer (Rangifer tarandus tarandus) in Finnmark, Norway, and their Relation to Climatic Conditions

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Global change and species interactions in terrestrial ecosystems

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Using host associations to predict spatial patterns in the species richness of the parasites of North American carnivores

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The importance of biotic interactions for modelling species distributions under climate change

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Increasing range mismatching of interacting species under global change is related to their ecological characteristics

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The role of biotic interactions in shaping distributions and realised assemblages of species: implications for species distribution modelling

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ENVIRONMENTAL NICHE EQUIVALENCY VERSUS CONSERVATISM: QUANTITATIVE APPROACHES TO NICHE EVOLUTION

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Combining static and dynamic variables in species distribution models under climate change

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THE INCIDENCE, DEVELOPMENT, AND EXPERIMENTAL TRANSMISSION OF PNEUMOSTRONGYLUS TENUIS DOUGHERTY (METASTRONGYLOIDEA: PROTOSTRONGYLIDAE) OF THE MENINGES OF THE WHITE-TAILED DEER (ODOCOILEUS VIRGINIANUS BOREALIS) IN ONTARIO

inferredcites →https://doi.org/10.1139/z68-055openalex-snapshot

Gastropods as intermediate hosts of Pneumostrongylus tenuis Dougherty of white-tailed deer

inferredcites →https://doi.org/10.1139/z74-048openalex-snapshot

Search for elaphostrongyline parasites in cervids from Alberta

inferredcites →https://doi.org/10.1139/z97-244openalex-snapshot

Over-winter survival of first-stage larvae ofParelaphostrongylus tenuis (Nematoda: Protostrongylidae)

inferredcites →https://doi.org/10.1146/annurev.ecolsys.37.091305.110100openalex-snapshot

Ecological and Evolutionary Responses to Recent Climate Change

inferredcites →https://doi.org/10.1186/1751-0147-52-51openalex-snapshot

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inferredcites →https://doi.org/10.1186/1751-0147-52-s1-s1openalex-snapshot

Climate change, parasites and shifting boundaries

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BioGeomancer: Automated Georeferencing to Map the World's Biodiversity Data

inferredcites →https://doi.org/10.1371/journal.pone.0000824openalex-snapshot

Malaria in Africa: Vector Species' Niche Models and Relative Risk Maps

inferredcites →https://doi.org/10.1371/journal.pone.0014236openalex-snapshot

A Broad Assessment of Factors Determining Culicoides imicola Abundance: Modelling the Present and Forecasting Its Future in Climate Change Scenarios

inferredcites →https://doi.org/10.1503/cmaj.081325openalex-snapshot

CMA opposes gender discrimination against doctors

inferredcites →https://doi.org/10.1515/9780691209418openalex-snapshot

Evolution in Changing Environments

inferredcites →https://doi.org/10.1890/07-1748.1openalex-snapshot

CLIMATE CHANGE CAN CAUSE SPATIAL MISMATCH OF TROPHICALLY INTERACTING SPECIES

inferredcites →https://doi.org/10.1890/07-2153.1openalex-snapshot

Sample selection bias and presence‐only distribution models: implications for background and pseudo‐absence data

inferredcites →https://doi.org/10.1890/08-0079.1openalex-snapshot

The ecology of climate change and infectious diseases

inferredcites →https://doi.org/10.1890/08-0616.1openalex-snapshot

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The ecology of climate change and infectious diseases: comment

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Pathogens, Nutritional Deficiency, and Climate Influences on a Declining Moose Population

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Modeling Distribution of Dispersal Distances in Male White‐Tailed Deer

inferredcites →https://doi.org/10.2307/3281873openalex-snapshot

Moisture and Temperature Effects on Survival and Infectivity of First-Stage Larvae of Parelaphostrongylus odocoilei and P. tenuis (Nematoda: Metastrongyloidea)

inferredcites →https://doi.org/10.2307/3282285openalex-snapshot

Terrestrial Gastropod Hosts of Parelaphostrongylus tenuis at the National Zoological Park's Conservation and Research Center, Virginia

inferredcites →https://doi.org/10.2307/3282899openalex-snapshot

Gastropod Intermediate Hosts of Parelaphostrongylus tenuis (Nematoda: Metastrongyloidea) from Northwestern Indiana

inferredcites →https://doi.org/10.2307/j.ctvx5wbbhopenalex-snapshot

Evolution in Changing Environments

inferredcites →https://doi.org/10.3354/dao02197openalex-snapshot

Future potential distribution of the emerging amphibian chytrid fungus under anthropogenic climate change

inferredcites →https://doi.org/10.7589/0090-3558-32.1.31openalex-snapshot

THE POSSIBLE IMPORTANCE OF WINTERING YARDS IN THE TRANSMISSION OF PARELAPHOSTRONGYLUS TENUIS TO WHITE-TAILED DEER AND MOOSE

inferredcites →https://doi.org/10.7589/0090-3558-39.2.338openalex-snapshot

DISTRIBUTION AND ECOLOGY OF MENINGEAL WORM, PARELAPHOSTRONGYLUS TENUIS (NEMATODA), IN NORTHCENTRAL NORTH AMERICA

inferredcites →https://doi.org/10.7589/0090-3558-8.4.304openalex-snapshot

THE ECOLOGICAL RELATIONSHIPS OF MENINGEAL WORM AND NATIVE CERVIDS IN NORTH AMERICA

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Additional file 1 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618205openalex-snapshot

Additional file 2 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618208openalex-snapshot

Additional file 3 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618211openalex-snapshot

Additional file 4 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618214openalex-snapshot

Additional file 5 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618217openalex-snapshot

Additional file 6 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618220openalex-snapshot

Additional file 7 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618223openalex-snapshot

Additional file 8 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.6084/m9.figshare.22618226openalex-snapshot

Additional file 9 of Cryptosporidiosis threat under climate change in China: prediction and validation of habitat suitability and outbreak risk for human-derived Cryptosporidium based on ecological niche models

inferred← citeshttps://doi.org/10.70675/da524fb3z25e6z4095zabc5zb6fbba47cc9copenalex-snapshot

Mécanismes d'infection de l'ectoparasite de poissons d'eau douce Tracheliastes polycolpus

inferred← citeshttps://doi.org/10.7287/peerj.2957v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Demographic, ecological, and physiological responses of ringed seals to an abrupt decline in sea ice availability (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.2957v0.1/reviews/2openalex-snapshot

Peer Review #2 of "Demographic, ecological, and physiological responses of ringed seals to an abrupt decline in sea ice availability (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.2957v0.1/reviews/3openalex-snapshot

Peer Review #3 of "Demographic, ecological, and physiological responses of ringed seals to an abrupt decline in sea ice availability (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.2957v0.2/reviews/1openalex-snapshot

Peer Review #1 of "Demographic, ecological, and physiological responses of ringed seals to an abrupt decline in sea ice availability (v0.2)"

inferred← citeshttps://doi.org/10.7287/peerj.2957v0.2/reviews/3openalex-snapshot

Peer Review #3 of "Demographic, ecological, and physiological responses of ringed seals to an abrupt decline in sea ice availability (v0.2)"

inferred← citeshttps://doi.org/10.7589/jwd-d-20-00060openalex-snapshot

EVALUATING THE THRESHOLD DENSITY HYPOTHESIS FOR MOOSE (ALCES ALCES), WHITE-TAILED DEER (ODOCOILEUS VIRGINIANUS), AND PARELAPHOSTRONGYLUS TENUIS

inferred← citeshttps://doi.org/10.7589/jwd-d-24-00076openalex-snapshot

HEALTH STATUS AND DRIVERS OF ENDOPARASITE INFECTION IN A LOW-DENSITY MOOSE (ALCES ALCES) POPULATION

inferred← citeshttps://doi.org/10.7717/peerj.2957openalex-snapshot

Demographic, ecological, and physiological responses of ringed seals to an abrupt decline in sea ice availability

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