On the public citation graph

Historical dynamics of Batrachochytrium dendrobatidis in Amazonia

https://doi.org/10.1111/ecog.02055

0 signed · 92 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/ece3.334openalex-snapshot

Temperature alters reproductive life history patterns in Batrachochytrium dendrobatidis, a lethal pathogen associated with the global loss of amphibians

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/s10393-006-0068-yopenalex-snapshot

Batrachochytrium dendrobatidis Infection in the Recently Rediscovered Atelopus mucubajiensis (Anura, Bufonidae), a Critically Endangered Frog from the Venezuelan Andes

inferredcites →https://doi.org/10.1007/s10393-010-0358-2openalex-snapshot

What Drives Chytrid Infections in Newt Populations? Associations with Substrate, Temperature, and Shade

inferredcites →https://doi.org/10.1007/s10531-010-9920-zopenalex-snapshot

A note on amphibian decline in a central Amazonian lowland forest

inferredcites →https://doi.org/10.1016/j.biocon.2014.12.007openalex-snapshot

A century of Batrachochytrium dendrobatidis in Illinois amphibians (1888–1989)

inferredcites →https://doi.org/10.1016/j.ecolmodel.2005.01.030openalex-snapshot

Predicting species distributions: use of climatic parameters in BIOCLIM and its impact on predictions of species’ current and future distributions

inferredcites →https://doi.org/10.1038/nature04246openalex-snapshot

Widespread amphibian extinctions from epidemic disease driven by global warming

inferredcites →https://doi.org/10.1073/pnas.0806368105openalex-snapshot

Evaluating the links between climate, disease spread, and amphibian declines

inferredcites →https://doi.org/10.1073/pnas.0912883107openalex-snapshot

Linking global climate and temperature variability to widespread amphibian declines putatively caused by disease

inferredcites →https://doi.org/10.1073/pnas.1014497108openalex-snapshot

Tropical amphibian populations experience higher disease risk in natural habitats

inferredcites →https://doi.org/10.1073/pnas.1105538108openalex-snapshot

Coincident mass extirpation of neotropical amphibians with the emergence of the infectious fungal pathogen Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.1073/pnas.95.15.9031openalex-snapshot

Chytridiomycosis causes amphibian mortality associated with population declines in the rain forests of Australia and Central America

inferredcites →https://doi.org/10.1080/03610929708831995openalex-snapshot

A spatial scan statistic

inferredcites →https://doi.org/10.1098/rspb.2012.2506openalex-snapshot

Climate, vegetation, introduced hosts and trade shape a global wildlife pandemic

inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01584.xopenalex-snapshot

Five (or so) challenges for species distribution modelling

inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05710.xopenalex-snapshot

Novel, panzootic and hybrid genotypes of amphibian chytridiomycosis associated with the bullfrog trade

inferredcites →https://doi.org/10.1111/j.1472-4642.2009.00618.xopenalex-snapshot

Widespread historical presence of Batrachochytrium dendrobatidis in African pipid frogs

inferredcites →https://doi.org/10.1111/j.1472-4642.2010.00725.xopenalex-snapshot

A statistical explanation of MaxEnt for ecologists

inferredcites →https://doi.org/10.1111/j.1523-1739.2005.00108.xopenalex-snapshot

Historical Evidence of Widespread Chytrid Infection in North American Amphibian Populations

inferredcites →https://doi.org/10.1111/j.1523-1739.2010.01604.xopenalex-snapshot

Batrachochytrium dendrobatidis and the Collapse of Anuran Species Richness and Abundance in the Upper Manu National Park, Southeastern Peru

inferredcites →https://doi.org/10.1111/j.1523-1739.2011.01728.xopenalex-snapshot

Environmental Refuge from Disease‐Driven Amphibian Extinction

inferredcites →https://doi.org/10.1111/j.1600-0587.2009.06299.xopenalex-snapshot

SAM: a comprehensive application for Spatial Analysis in Macroecology

inferredcites →https://doi.org/10.1111/j.1600-0587.2012.07877.xopenalex-snapshot

Evaluating multiple causes of amphibian declines of Ecuador using geographical quantitative analyses

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.2006.0906-7590.04596.xopenalex-snapshot

Novel methods improve prediction of species’ distributions from occurrence data

inferredcites →https://doi.org/10.1111/mec.12615openalex-snapshot

Long‐term endemism of two highly divergent lineages of the amphibian‐killing fungus in the A tlantic F orest of B razil

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.pone.0048205openalex-snapshot

Disease Risk in Temperate Amphibian Populations Is Higher at Closed-Canopy Sites

inferredcites →https://doi.org/10.1371/journal.pone.0063791openalex-snapshot

Prevalence of Batrachochytrium dendrobatidis in Xenopus Collected in Africa (1871–2000) and in California (2001–2010)

inferredcites →https://doi.org/10.1371/journal.pone.0073830openalex-snapshot

Variation in Thermal Performance of a Widespread Pathogen, the Amphibian Chytrid Fungus Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.1371/journal.pone.0125128openalex-snapshot

Widespread Occurrence of Bd in French Guiana, South America

inferredcites →https://doi.org/10.1641/0006-3568(2002)052[0891:thfatl]2.0.co;2openalex-snapshot

The Human Footprint and the Last of the Wild

inferredcites →https://doi.org/10.2994/sajh-d-13-00022.1openalex-snapshot

Systematics of the Neotropical GenusLeptodactylusFitzinger, 1826 (Anura: Leptodactylidae): Phylogeny, the Relevance of Non-molecular Evidence, and Species Accounts

inferredcites →https://doi.org/10.3201/eid1012.030804openalex-snapshot

Origin of the Amphibian Chytrid Fungus

inferredcites →https://doi.org/10.3354/dao02845openalex-snapshot

Chytrid fungus acts as a generalist pathogen infecting species-rich amphibian families in Brazilian rainforests

inferredcites →https://doi.org/10.3354/dao073175openalex-snapshot

Diagnostic assays and sampling protocols for the detection of Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.3354/dao073257openalex-snapshot

On the biological relevance of a single Batrachochytrium dendrobatidis zoospore: a reply to Smith (2007)

inferredcites →https://doi.org/10.3390/d1010052openalex-snapshot

Global Amphibian Extinction Risk Assessment for the Panzootic Chytrid Fungus

inferredcites →https://doi.org/10.5061/dryad.h3112openalex-snapshot

Data from: Historical dynamics of Batrachochytrium dendrobatidis in Amazonia

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4803698openalex-extracted

Historical Evidence and the Global Frog Trade Suggest a New Hypothesis Regarding the Origin and Spread of a Chytrid Fungus Lineage

inferred← citeshttps://doi.org/10.1002/ece3.9998openalex-snapshot

Leveraging preserved specimens of Nerodia to infer the spatiotemporal dynamics of Ophidiomyces ophidiicola via quantitative polymerase chain reaction

inferred← citeshttps://doi.org/10.1002/ecs2.2724openalex-snapshot

The amphibian‐killing fungus in a biodiversity hotspot: identifying and validating high‐risk areas and refugia

inferred← citeshttps://doi.org/10.1007/978-3-030-26296-9_7openalex-snapshot

Spatial Conservation Prioritization for the Anuran Fauna of South America

inferred← citeshttps://doi.org/10.1007/978-3-031-50531-7_3openalex-snapshot

Emerging Infectious Diseases and Their Impacts on South American Amphibians

inferred← citeshttps://doi.org/10.1007/s00442-020-04646-4openalex-snapshot

Assessing amphibian disease risk across tropical streams while accounting for imperfect pathogen detection

inferred← citeshttps://doi.org/10.1007/s10393-025-01698-xopenalex-snapshot

Climatically Specialized Lineages of Batrachochytrium dendrobatidis, and its Likely Asian Origins

inferred← citeshttps://doi.org/10.1007/s10393-025-01716-yopenalex-snapshot

Community-Wide Genotyping of Batrachochytrium dendrobatidis in Ecuadorian Forests

inferred← citeshttps://doi.org/10.1007/s10661-023-11997-xopenalex-snapshot

Climate change in the Central Amazon and its impacts on frog populations

inferred← citeshttps://doi.org/10.1007/s10750-017-3367-0openalex-snapshot

Stream tadpoles present high prevalence but low infection loads of Batrachochytrium dendrobatidis (Chytridiomycota)

inferred← citeshttps://doi.org/10.1007/s10750-020-04339-2openalex-snapshot

High temporal and individual variation in the prevalence and intensity of chytrid infection in the southernmost Leaf Frog of the genus Pithecopus (Anura, Phyllomedusidae)

inferred← citeshttps://doi.org/10.1016/j.biocon.2022.109845openalex-snapshot

A retrospective overview of amphibian declines in Brazil's Atlantic Forest

inferred← citeshttps://doi.org/10.1016/j.biocon.2025.111547openalex-snapshot

Origin and global spread of an endemic chytrid fungus lineage linked to the bullfrog trade

inferred← citeshttps://doi.org/10.1016/j.cub.2026.09.048openalex-snapshot

The chytrid fungus threatens the last epidemiologically naive Neotropical montane amphibian biodiversity hotspot

inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101546openalex-snapshot

Host life stage susceptibility to the chytrid fungus in a Neotropical torrent frog

inferred← citeshttps://doi.org/10.1016/j.funeco.2016.11.007openalex-snapshot

Variation in phenotype and virulence among enzootic and panzootic amphibian chytrid lineages

inferred← citeshttps://doi.org/10.1016/j.funeco.2020.100995openalex-snapshot

Biotic and abiotic determinants of Batrachochytrium dendrobatidis infections in amphibians of the Brazilian Atlantic Forest

inferred← citeshttps://doi.org/10.1016/j.jnc.2025.126996openalex-snapshot

Chytrid fungus in threatened Brazilian amphibians: A focus on island populations

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2020.102653openalex-snapshot

Variation of body temperature of active amphibians along elevation gradients in eastern Nepal Himalaya

inferred← citeshttps://doi.org/10.1016/s2542-5196(24)00163-3openalex-snapshot

A road to the next pandemic: the consequences of Amazon highway BR-319 for planetary health

inferred← citeshttps://doi.org/10.1038/s41598-018-21879-9openalex-snapshot

The influence of riverine barriers, climate, and topography on the biogeographic regionalization of Amazonian anurans

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/s41598-020-79130-3openalex-snapshot

Skin microbiome correlates with bioclimate and Batrachochytrium dendrobatidis infection intensity in Brazil’s Atlantic Forest treefrogs

inferred← citeshttps://doi.org/10.1038/s41598-022-16664-8openalex-snapshot

Comparative host–pathogen associations of Snake Fungal Disease in sympatric species of water snakes (Nerodia)

inferred← citeshttps://doi.org/10.1079/cabicompendium.109124openalex-snapshot

Batrachochytrium dendrobatidis (Bd)

inferred← citeshttps://doi.org/10.1080/01650521.2016.1163857openalex-snapshot

Crossing the threshold: an amphibian assemblage highly infected with Batrachochytrium dendrobatidis in the southern Brazilian Atlantic forest

inferred← citeshttps://doi.org/10.1080/21564574.2021.1998235openalex-snapshot

Fatal chytridiomycosis in the Moroccan midwife toad Alytes maurus and potential distribution of Batrachochytrium dendrobatidis across Morocco

inferred← citeshttps://doi.org/10.1093/conphys/coaa047openalex-snapshot

Changes in physiology and microbial diversity in larval ornate chorus frogs are associated with habitat quality

inferred← citeshttps://doi.org/10.1098/rsos.252148openalex-snapshot

Evaluating bromeliads as environmental reservoirs for Batrachochytrium dendrobatidis and amphibian disease dynamics in equatorial forests

inferred← citeshttps://doi.org/10.1098/rspb.2016.2254openalex-snapshot

Historical amphibian declines and extinctions in Brazil linked to chytridiomycosis

inferred← citeshttps://doi.org/10.1098/rspb.2019.1114openalex-snapshot

Low-load pathogen spillover predicts shifts in skin microbiome and survival of a terrestrial-breeding amphibian

inferred← citeshttps://doi.org/10.1101/2023.01.23.525302openalex-snapshot

New climatically specialized lineages of Batrachochytrium dendrobatidis and their sub-lethal effects on amphibians establish the Asiatic origins of the pathogen

inferred← citeshttps://doi.org/10.1101/2024.02.16.580711openalex-snapshot

Elevated prevalence of the global panzootic chytrid strain in Ecuadorian anurans of the Amazonian lowlands

inferred← citeshttps://doi.org/10.1111/btp.12457openalex-snapshot

Current and predicted distribution of the pathogenic fungus Batrachochytrium dendrobatidis in Colombia, a hotspot of amphibian biodiversity

inferred← citeshttps://doi.org/10.1111/ecog.05977openalex-snapshot

Synthesis of Batrachochytrium dendrobatidis infection in South America: amphibian species under risk and areas to focus research and disease mitigation

inferred← citeshttps://doi.org/10.1111/jzs.12390openalex-snapshot

Urban growth threatens the lowland Amazonian Manaus harlequin frog which represents an evolutionarily significant unit within the genus Atelopus (Amphibia: Anura: Bufonidae)

inferred← citeshttps://doi.org/10.1177/1940082918797057openalex-snapshot

Microhabitat Temperatures and Prevalence of the Pathogenic Fungus Batrachochytrium dendrobatidis in Lowland Amazonian Frogs

inferred← citeshttps://doi.org/10.1177/1940082919892626openalex-snapshot

Worrying News for Brazilian Caatinga: Prevalence of Batrachochytrium dendrobatidis in Amphibians

inferred← citeshttps://doi.org/10.21931/rb/2021.06.01.28openalex-snapshot

Amphibian chytridiomycosis, a lethal pandemic disease caused by the killer fungus Batrachochytrium dendrobatidis: New approaches to host defense mechanisms and techniques for detection and monitoring

inferred← citeshttps://doi.org/10.2994/sajh-d-22-00032.1openalex-snapshot

Detection of the Fungus Batrachochytrium dendrobatidis in Anurans from the Semiarid Region of Brazil: new Infection Records for Endemic Species

inferred← citeshttps://doi.org/10.3354/dao03114openalex-snapshot

Spatial distribution of Batrachochytrium dendrobatidis in South American caecilians

inferred← citeshttps://doi.org/10.3354/dao03402openalex-snapshot

New records of Batrachochytrium dendrobatidis in the state of Bahia, Brazil: histological analysis in anuran amphibian collections

inferred← citeshttps://doi.org/10.3354/dao03709openalex-snapshot

Chytrid fungus in amphibians from the lowland Brazilian Amazon

inferred← citeshttps://doi.org/10.3354/dao03830openalex-snapshot

Detection of the Batrachochytrium dendrobatidis global panzootic lineage in Ecuadorian anurans of the Amazonian lowlands

inferred← citeshttps://doi.org/10.3389/fvets.2021.791237openalex-snapshot

Prevalence of Batrachochytrium dendrobatidis in Amphibians From 2000 to 2021: A Global Systematic Review and Meta-Analysis

inferred← citeshttps://doi.org/10.7287/peerj.4941v0.1/reviews/1openalex-snapshot

Peer Review #1 of "A Pan-Amazonian species delimitation: high species diversity within the genus Amazophrynella (Anura: Bufonidae) (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.4941v0.1/reviews/2openalex-snapshot

Peer Review #2 of "A Pan-Amazonian species delimitation: high species diversity within the genus Amazophrynella (Anura: Bufonidae) (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.4941v0.1/reviews/3openalex-snapshot

Peer Review #3 of "A Pan-Amazonian species delimitation: high species diversity within the genus Amazophrynella (Anura: Bufonidae) (v0.1)"

inferred← citeshttps://doi.org/10.7589/jwd-d-24-00068openalex-snapshot

EPIZOOTIC OF CLINOSTOMUM MARGINATUM (TREMATODA: CLINOSTOMIDAE) IN AMBYSTOMA TIGRINUM FROM COLORADO, USA: INVESTIGATION THROUGH GENOMICS, HISTOPATHOLOGY, AND NONINVASIVE IMAGERY

inferred← citeshttps://doi.org/10.7589/jwd-d-25-00033openalex-snapshot

CONTRASTING SEASONAL PREVALENCE OF BATRACHOCHYTRIUM DENDROBATIDIS ON ANURANS IN FRAGMENTED URBAN FORESTS

inferred← citeshttps://doi.org/10.7717/peerj.4941openalex-snapshot

A Pan-Amazonian species delimitation: high species diversity within the genus Amazophrynella (Anura: Bufonidae)

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.