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

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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/joc.1276openalex-snapshot
Very high resolution interpolated climate surfaces for global land areas
inferredcites →https://doi.org/10.1007/s003820050010openalex-snapshot
The simulation of SST, sea ice extents and ocean heat transports in a version of the Hadley Centre coupled model without flux adjustments
inferredcites →https://doi.org/10.1007/s003820050339openalex-snapshot
The Canadian Centre for Climate Modelling and Analysis global coupled model and its climate
inferredcites →https://doi.org/10.1007/s10393-007-0093-5openalex-snapshot
Spread of Chytridiomycosis Has Caused the Rapid Global Decline and Extinction of Frogs
inferredcites →https://doi.org/10.1016/j.ecolmodel.2005.03.026openalex-snapshot
Maximum entropy modeling of species geographic distributions
inferredcites →https://doi.org/10.1016/j.tree.2006.09.010openalex-snapshot
Ensemble forecasting of species distributions
inferredcites →https://doi.org/10.1038/climate.2008.37openalex-snapshot
Beware the lone killer
inferredcites →https://doi.org/10.1038/nature01286openalex-snapshot
A globally coherent fingerprint of climate change impacts across natural systems
inferredcites →https://doi.org/10.1038/nature04246openalex-snapshot
Widespread amphibian extinctions from epidemic disease driven by global warming
inferredcites →https://doi.org/10.1038/nature05940openalex-snapshot
Global warming and amphibian losses
inferredcites →https://doi.org/10.1038/nature05942openalex-snapshot
Global warming and amphibian losses; The proximate cause of frog declines? (Reply)
inferredcites →https://doi.org/10.1046/j.1365-2664.2001.00647.xopenalex-snapshot
Evaluating presence–absence models in ecology: the need to account for prevalence
inferredcites →https://doi.org/10.1073/pnas.0801921105openalex-snapshot
Are we in the midst of the sixth mass extinction? A view from the world of amphibians
inferredcites →https://doi.org/10.1073/pnas.0806368105openalex-snapshot
Evaluating the links between climate, disease spread, and amphibian declines
inferredcites →https://doi.org/10.1080/00222930903100550openalex-snapshot
Translating natural history into geographic space: a macroecological perspective on the North American Slider,Trachemys scripta(Reptilia, Cryptodira, Emydidae)
inferredcites →https://doi.org/10.1098/rspb.2006.3713openalex-snapshot
Climate change and outbreaks of amphibian chytridiomycosis in a montane area of Central Spain; is there a link?
inferredcites →https://doi.org/10.1111/j.0906-7590.2006.04700.xopenalex-snapshot
The effect of sample size and species characteristics on performance of different species distribution modeling methods
inferredcites →https://doi.org/10.1111/j.0906-7590.2008.5203.xopenalex-snapshot
Modeling of species distributions with Maxent: new extensions and a comprehensive evaluation
inferredcites →https://doi.org/10.1111/j.0906-7590.2008.5378.xopenalex-snapshot
Transferability, sample selection bias and background data in presence‐only modelling: a response to Peterson et al. (2007)
inferredcites →https://doi.org/10.1111/j.1365-2486.2004.00828.xopenalex-snapshot
Would climate change drive species out of reserves? An assessment of existing reserve‐selection methods
inferredcites →https://doi.org/10.1111/j.1365-2486.2006.01278.xopenalex-snapshot
Upward range extension of Andean anurans and chytridiomycosis to extreme elevations in response to tropical deglaciation
inferredcites →https://doi.org/10.1111/j.1442-9993.2007.01812.xopenalex-snapshot
Global warming and amphibian extinctions in eastern Australia
inferredcites →https://doi.org/10.1111/j.1466-8238.2009.00477.xopenalex-snapshot
Niche shift versus niche conservatism? Climatic characteristics of the native and invasive ranges of the Mediterranean house gecko (Hemidactylus turcicus)
inferredcites →https://doi.org/10.1111/j.1469-1795.2008.00210.xopenalex-snapshot
Environmental gradients explaining the prevalence and intensity of infection with the amphibian chytrid fungus: the host's perspective
inferredcites →https://doi.org/10.1111/j.1469-1795.2009.00297.xopenalex-snapshot
Widespread occurrence of the amphibian chytrid fungus in Kenya
inferredcites →https://doi.org/10.1111/j.1469-7998.2006.00220.xopenalex-snapshot
Large‐scale seasonal variation in the prevalence and severity of chytridiomycosis
inferredcites →https://doi.org/10.1111/j.1523-1739.2005.004403.xopenalex-snapshot
Ecology of Chytridiomycosis in Rainforest Stream Frog Assemblages of Tropical Queensland
inferredcites →https://doi.org/10.1111/j.1523-1739.2007.00777.xopenalex-snapshot
Latitudinal Variation in the Prevalence and Intensity of Chytrid ( Batrachochytrium dendrobatidis ) Infection in Eastern Australia
inferredcites →https://doi.org/10.1111/j.1744-7429.2005.00028.xopenalex-snapshot
Predicting the Distribution of the Amphibian Pathogen Batrachochytrium dendrobatidis in the New World 1
inferredcites →https://doi.org/10.1111/j.1755-263x.2008.00015.xopenalex-snapshot
Predicting susceptibility to future declines in the world's frogs
inferredcites →https://doi.org/10.1111/j.2006.0906-7590.04596.xopenalex-snapshot
Novel methods improve prediction of species’ distributions from occurrence data
inferredcites →https://doi.org/10.1126/science.1128396openalex-snapshot
Confronting Amphibian Declines and Extinctions
inferredcites →https://doi.org/10.1126/science.1155193openalex-snapshot
Aligning Conservation Priorities Across Taxa in Madagascar with High-Resolution Planning Tools
inferredcites →https://doi.org/10.1126/science.3287615openalex-snapshot
Measuring the Accuracy of Diagnostic Systems
inferredcites →https://doi.org/10.1146/annurev.ecolsys.37.091305.110100openalex-snapshot
Ecological and Evolutionary Responses to Recent Climate Change
inferredcites →https://doi.org/10.1146/annurev.micro.091208.073435openalex-snapshot
Global Emergence of Batrachochytrium dendrobatidis and Amphibian Chytridiomycosis in Space, Time, and Host
inferredcites →https://doi.org/10.1371/journal.pbio.0060072openalex-snapshot
Riding the Wave: Reconciling the Roles of Disease and Climate Change in Amphibian Declines
inferredcites →https://doi.org/10.1371/journal.pbio.0060118openalex-snapshot
The Challenge of Conserving Amphibian Megadiversity in Madagascar
inferredcites →https://doi.org/10.1371/journal.pone.0000176openalex-snapshot
Ecological Niche and Geographic Distribution of Human Monkeypox in Africa
inferredcites →https://doi.org/10.1371/journal.pone.0007843openalex-snapshot
Alien Invasive Slider Turtle in Unpredicted Habitat: A Matter of Niche Shift or of Predictors Studied?
inferredcites →https://doi.org/10.1890/0012-9658(2006)87[1671:eidaap]2.0.co;2openalex-snapshot
EMERGING INFECTIOUS DISEASE AS A PROXIMATE CAUSE OF AMPHIBIAN MASS MORTALITY
inferredcites →https://doi.org/10.1890/06-1842.1openalex-snapshot
LIFE-HISTORY TRADE-OFFS INFLUENCE DISEASE IN CHANGING CLIMATES: STRATEGIES OF AN AMPHIBIAN PATHOGEN
inferredcites →https://doi.org/10.1890/08-0079.1openalex-snapshot
The ecology of climate change and infectious diseases
inferredcites →https://doi.org/10.2307/3761981openalex-snapshot
Physiology of Batrachochytrium dendrobatidis, a Chytrid Pathogen of Amphibians
inferredcites →https://doi.org/10.3390/d1010052openalex-snapshot
Global Amphibian Extinction Risk Assessment for the Panzootic Chytrid Fungus
inferredcites →https://doi.org/10.7589/0090-3558-44.3.716openalex-snapshot
Effect of Temperature on Host Response to Batrachochytrium dendrobatidis Infection in the Mountain Yellow-legged Frog (Rana muscosa)

What points at this work

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

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New species, diversity, systematics, and conservation assessment of the Puppet Toads of Sumatra (Anura: Bufonidae: Sigalegalephrynus)
inferred← citeshttps://doi.org/10.2139/ssrn.4795486openalex-extracted
Understanding and Predicting Disease Dynamics for an Endangered Amphibian Using Long-Term Surveys of Wild and Translocated Frogs
inferred← citeshttps://doi.org/10.1002/eap.70222openalex-snapshot
Multiscale habitat modeling to improve spatial prioritization for mugger crocodile conservation in riverine landscapes
inferred← citeshttps://doi.org/10.1002/ece3.5098openalex-snapshot
Infection with Batrachochytrium dendrobatidis is common in tropical lowland habitats: Implications for amphibian conservation
inferred← citeshttps://doi.org/10.1002/ece3.8798openalex-snapshot
Widespread occurrence of Batrachochytrium dendrobatidis in Ontario, Canada, and predicted habitat suitability for the emerging Batrachochytrium salamandrivorans
inferred← citeshttps://doi.org/10.1002/edn3.70271openalex-snapshot
Unraveling the Environmental Drivers of Chytrid Fungal eDNA Detection and Quantity in Rainforest Streams
inferred← citeshttps://doi.org/10.1007/978-1-4939-2208-6_14openalex-snapshot
Conservation of a Neotropical Herpetofauna: An Introduction to the Crisis of Amphibians and Reptiles in Central America and Beyond
inferred← citeshttps://doi.org/10.1007/978-3-031-83903-0_22openalex-snapshot
Climate Change and Parasitism in Aquatic Ecosystems
inferred← citeshttps://doi.org/10.1007/978-3-642-20992-5_14openalex-snapshot
Hotspots, Conservation, and Diseases: Madagascar’s Megadiverse Amphibians and the Potential Impact of Chytridiomycosis
inferred← citeshttps://doi.org/10.1007/s10393-021-01519-xopenalex-snapshot
Spatial Risk Analysis of Batrachochytrium dendrobatidis, A Global Emerging Fungal Pathogen
inferred← citeshttps://doi.org/10.1007/s10393-021-01522-2openalex-snapshot
First Detection of Batrachochytrium dendrobatidis in Wild Frogs from Bangladesh
inferred← citeshttps://doi.org/10.1007/s10393-023-01631-0openalex-snapshot
Water Pollution Increases the Risk of Chytridiomycosis in Mexican Amphibians
inferred← citeshttps://doi.org/10.1007/s10393-023-01668-1openalex-snapshot
Batrachochytrium dendrobatidis in the Arid and Thermally Extreme Sonoran Desert
inferred← citeshttps://doi.org/10.1007/s13744-025-01325-yopenalex-snapshot
Precipitation and Interannual Variability Shape the Phenology and Abundance of the Endangered Butterfly Baronia brevicornis
inferred← citeshttps://doi.org/10.1007/s41745-021-00227-3openalex-snapshot
Chytridiomycosis in Asian Amphibians, a Global Resource for Batrachochytrium dendrobatidis (Bd) Research
inferred← citeshttps://doi.org/10.1016/b978-0-12-384703-4.00406-8openalex-snapshot
Does Climate Change Increase the Risk of Disease? Analyzing Published Literature to Detect Climate–Disease Interactions
inferred← citeshttps://doi.org/10.1016/j.biocon.2024.110834openalex-snapshot
Understanding and predicting infection dynamics for an endangered amphibian using long-term surveys of wild and translocated frogs
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2021.104630openalex-snapshot
Biological control of Parkinsonia aculeata: Using species distribution models to refine agent surveys and releases
inferred← citeshttps://doi.org/10.1016/j.cvex.2013.01.005openalex-snapshot
Selected Emerging Diseases of Amphibia
inferred← citeshttps://doi.org/10.1016/j.ecoinf.2012.11.005openalex-snapshot
Modelling fungus dispersal scenarios using cellular automata
inferred← citeshttps://doi.org/10.1016/j.funbio.2022.10.004openalex-snapshot
Global niche and range shifts of Batrachochytrium dendrobatidis, a highly virulent amphibian-killing fungus
inferred← citeshttps://doi.org/10.1016/j.funeco.2015.09.007openalex-snapshot
History and recent progress on chytridiomycosis in amphibians
inferred← citeshttps://doi.org/10.1016/j.funeco.2015.09.014openalex-snapshot
Local phenotypic variation in amphibian-killing fungus predicts infection dynamics
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106192openalex-snapshot
Biological mechanisms matter in contemporary wildlife conservation
inferred← citeshttps://doi.org/10.1016/j.jnc.2026.127387openalex-snapshot
Identifying climatic disease refuges from the fungal skin pathogen Batrachochytrium dendrobatidis for Harlequin toads (Atelopus spp.) in Panama
inferred← citeshttps://doi.org/10.1017/s0030605316000612openalex-snapshot
Recent and future threats to the Endangered Cuban toad Peltophryne longinasus: potential additive impacts of climate change and habitat loss
inferred← citeshttps://doi.org/10.1038/480461aopenalex-snapshot
Bleak future for amphibians
inferred← citeshttps://doi.org/10.1038/nature10650openalex-snapshot
Additive threats from pathogens, climate and land-use change for global amphibian diversity
inferred← citeshttps://doi.org/10.1038/s41467-018-06157-6openalex-snapshot
Quantifying climate sensitivity and climate-driven change in North American amphibian communities
inferred← citeshttps://doi.org/10.1038/s41598-018-27828-wopenalex-snapshot
Hybrids of amphibian chytrid show high virulence in native hosts
inferred← citeshttps://doi.org/10.1038/s41598-018-28304-1openalex-snapshot
Enzootic frog pathogen Batrachochytrium dendrobatidis in Asian tropics reveals high ITS haplotype diversity and low prevalence
inferred← citeshttps://doi.org/10.1038/s41598-021-96535-wopenalex-snapshot
Bioclimatic and anthropogenic variables shape the occurrence of Batrachochytrium dendrobatidis over a large latitudinal gradient
inferred← citeshttps://doi.org/10.1038/srep25625openalex-snapshot
Quantitative evidence for the effects of multiple drivers on continental-scale amphibian declines
inferred← citeshttps://doi.org/10.1039/9781837672004-00006openalex-snapshot
Considerations of Amphibian Models and Testing Paradigms for Ecological Risk Assessment
inferred← citeshttps://doi.org/10.1080/00275514.2026.2660613openalex-snapshot
Free-living fungi in the Anthropocene and impacts on public health, food security, and biodiversity
inferred← citeshttps://doi.org/10.1080/21564574.2022.2115154openalex-snapshot
An inventory of amphibian roadkill in the western Soutpansberg, Limpopo province, South Africa
inferred← citeshttps://doi.org/10.1093/jmammal/gyac017openalex-snapshot
Modeling the suitability of Texas karst regions for infection by Pseudogymnoascus destructans in bats
inferred← citeshttps://doi.org/10.1098/rsos.160975openalex-snapshot
Accuracy of climate-based forecasts of pathogen spread
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Climate, vegetation, introduced hosts and trade shape a global wildlife pandemic
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Climatic niche evolution of infectious diseases driving amphibian declines
inferred← citeshttps://doi.org/10.1111/1749-4877.12001openalex-snapshot
Review and synthesis of the effects of climate change on amphibians
inferred← citeshttps://doi.org/10.1111/btp.12697openalex-snapshot
Known and estimated distribution in Mexico of Batrachochytrium dendrobatidis, a pathogenic fungus of amphibians
inferred← citeshttps://doi.org/10.1111/ddi.13533openalex-snapshot
Predicting the distribution of Australian frogs and their overlap with Batrachochytrium dendrobatidis under climate change
inferred← citeshttps://doi.org/10.1111/gcb.12255openalex-snapshot
Predicting shifts in parasite distribution with climate change: a multitrophic level approach
inferred← citeshttps://doi.org/10.1111/j.1472-4642.2011.00878.xopenalex-snapshot
Global and endemic Asian lineages of the emerging pathogenic fungus Batrachochytrium dendrobatidis widely infect amphibians in China
inferred← citeshttps://doi.org/10.1111/j.1600-0587.2012.07877.xopenalex-snapshot
Evaluating multiple causes of amphibian declines of Ecuador using geographical quantitative analyses
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Temporal Variation in Infection Prevalence by the Amphibian Chytrid Fungus in Three Species of Frogs at La Selva, Costa Rica
inferred← citeshttps://doi.org/10.1111/jeb.13413openalex-snapshot
Diverse genotypes of the amphibian‐killing fungus produce distinct phenotypes through plastic responses to temperature
inferred← citeshttps://doi.org/10.1111/mec.12385openalex-snapshot
Genetic evidence for a high diversity and wide distribution of endemic strains of the pathogenic chytrid fungus B atrachochytrium dendrobatidisin wild A sian amphibians
inferred← citeshttps://doi.org/10.1186/s12862-023-02132-yopenalex-snapshot
The two chytrid pathogens of amphibians in Eurasia—climatic niches and future expansion
inferred← citeshttps://doi.org/10.12688/f1000research.8766.1openalex-snapshot
The rise and fall of infectious disease in a warmer world
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Short-term temperature fluctuations increase disease in a Daphnia-parasite infectious disease system
inferred← citeshttps://doi.org/10.1371/journal.pone.0023179openalex-snapshot
Is Chytridiomycosis an Emerging Infectious Disease in Asia?
inferred← citeshttps://doi.org/10.1371/journal.pone.0056236openalex-snapshot
West Africa - A Safe Haven for Frogs? A Sub-Continental Assessment of the Chytrid Fungus (Batrachochytrium dendrobatidis)
inferred← citeshttps://doi.org/10.1371/journal.pone.0145841openalex-snapshot
Assessing the Threat of Amphibian Chytrid Fungus in the Albertine Rift: Past, Present and Future
inferred← citeshttps://doi.org/10.1371/journal.pone.0160746openalex-snapshot
Projecting the Global Distribution of the Emerging Amphibian Fungal Pathogen, Batrachochytrium dendrobatidis, Based on IPCC Climate Futures
inferred← citeshttps://doi.org/10.1371/journal.pone.0199288openalex-snapshot
Distribution modeling and lineage diversity of the chytrid fungus Batrachochytrium dendrobatidis (Bd) in a central African amphibian hotspot
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Spatially explicit cost-effective actions for biodiversity threat abatement
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Uma nova abordagem para modelagem de distribuição de espécies a partir de registros restritos: aplicação em projeções de padrões futuros de formigas do cerrado
inferred← citeshttps://doi.org/10.1515/acve-2017-0042openalex-snapshot
Emerging Chytrid Fungal Pathogen, Batrachochytrium Dendrobatidis, in Zoo Amphibians in Thailand
inferred← citeshttps://doi.org/10.1655/herpetologica-d-15-00013openalex-snapshot
Seasonality, Environmental Factors, and Host Behavior Linked to Disease Risk in Stream-Dwelling Tadpoles
inferred← citeshttps://doi.org/10.17638/02032659openalex-snapshot
The impact of climate change on the distribution and conservation status of African antelopes
inferred← citeshttps://doi.org/10.2139/ssrn.5817802openalex-snapshot
Identifying climatic disease refuges from the fungal skin pathogen Batrachochytrium dendrobatidis for Harlequin toads (Atelopus spp.) in Panama
inferred← citeshttps://doi.org/10.3354/dao02369openalex-snapshot
New records of Batrachochytrium dendrobatidis in Chilean frogs
inferred← citeshttps://doi.org/10.3354/dao02662openalex-snapshot
Batrachochytrium dendrobatidis in Germany: distribution, prevalences, and prediction of high risk areas
inferred← citeshttps://doi.org/10.3354/dao03709openalex-snapshot
Chytrid fungus in amphibians from the lowland Brazilian Amazon
inferred← citeshttps://doi.org/10.3389/fevo.2019.00254openalex-snapshot
Mitigating Disease Impacts in Amphibian Populations: Capitalizing on the Thermal Optimum Mismatch Between a Pathogen and Its Host
inferred← citeshttps://doi.org/10.3389/fevo.2020.576065openalex-snapshot
Predictions of Disease Risk in Space and Time Based on the Thermal Physiology of an Amphibian Host-Pathogen Interaction
inferred← citeshttps://doi.org/10.3389/fvets.2021.685877openalex-snapshot
Global Patterns of the Fungal Pathogen Batrachochytrium dendrobatidis Support Conservation Urgency
inferred← citeshttps://doi.org/10.33915/etd.11188openalex-snapshot
Assessment of the Geographic Distribution and Tools to Assist with Conservation of Spotted Turtles (Clemmys guttata) in West Virginia
inferred← citeshttps://doi.org/10.3897/zookeys.1062.66913openalex-snapshot
Amphibian fauna of Pakistan with notes on future prospects of research and conservation
inferred← citeshttps://doi.org/10.47749/t/unicamp.2019.1157384openalex-snapshot
Padrões de ocorrência de Batrachochytrium dendrobatidis em anfíbios da Mata Atlântica e Amazônia brasileiras
inferred← citeshttps://doi.org/10.6084/m9.figshare.23590420openalex-snapshot
Additional file 1 of The two chytrid pathogens of amphibians in Eurasia—climatic niches and future expansion
inferred← citeshttps://doi.org/10.6084/m9.figshare.23590423openalex-snapshot
Additional file 2 of The two chytrid pathogens of amphibians in Eurasia—climatic niches and future expansion
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