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Possible modes of dissemination of the amphibian chytrid Batrachochytrium dendrobatidis in the environment
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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/jobm.3620340202openalex-snapshot
Oomycetes and Chytridiomycetes (Mastigomycotina) from water bodies in Tübingen region (Germany)
inferredcites →https://doi.org/10.1016/s0006-3207(00)00132-4openalex-snapshot
Evidence of a chytrid fungus infection involved in the decline of the common midwife toad (Alytes obstetricans) in protected areas of central Spain
inferredcites →https://doi.org/10.1016/s0007-1536(86)80148-6openalex-snapshot
Selective accumulation of zoospores of chytridiomycetes and oomycetes on cellulose and chitin
inferredcites →https://doi.org/10.1046/j.1523-1739.1996.10020406.xopenalex-snapshot
Epidemic Disease and the Catastrophic Decline of Australian Rain Forest Frogs
inferredcites →https://doi.org/10.1046/j.1523-1739.1997.96291.xopenalex-snapshot
Epidemic Disease and Amphibian Declines in Australia
inferredcites →https://doi.org/10.1046/j.1523-1739.1997.96403.xopenalex-snapshot
Lack of Evidence for Epidemic Disease as an Agent in the Catastrophic Decline of Australian Rain Forest Frogs
inferredcites →https://doi.org/10.1046/j.1523-1739.1997.97109.xopenalex-snapshot
In Defense of the Epidemic Disease Hypothesis
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/10.1139/b80-276openalex-snapshot
An outline for the reclassification of the Chytridiales, and for a new order, the Spizellomycetales
inferredcites →https://doi.org/10.1177/104063879901100219openalex-snapshot
Cutaneous Chytridiomycosis in Poison Dart Frogs ( Dendrobates spp.) and White's Tree Frogs ( Litoria Caerulea )
inferredcites →https://doi.org/10.1201/9781315380773openalex-snapshot
Plant Pathology Concepts and Laboratory Exercises
inferredcites →https://doi.org/10.2307/3761366openalex-snapshot
Batrachochytrium Dendrobatidis gen. et sp. nov., a Chytrid Pathogenic to Amphibians
inferredcites →https://doi.org/10.2307/3761981openalex-snapshot
Physiology of Batrachochytrium dendrobatidis, a Chytrid Pathogen of Amphibians
inferredcites →https://doi.org/10.3201/eid0908.030145openalex-snapshot
Survival ofBatrachochytrium dendrobatidisin Water: Quarantine and Disease Control Implications
inferredcites →https://doi.org/10.3354/dao057255openalex-snapshot
Fungicidal effects of chemical disinfectants, UV light, desiccation and heat on the amphibian chytrid Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.3354/dao060141openalex-snapshot
Rapid quantitative detection of chytridiomycosis (Batrachochytrium dendrobatidis) in amphibian samples using real-time Taqman PCR assay
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/neobiota.104.160230zenodo-depositor-declared
Comparing sampling protocols and results to better detect the amphibian fungal parasite Batrachochytrium dendrobatidis in the wild
inferred← citeshttps://doi.org/10.1002/aqc.3653openalex-snapshot
Improving breed‐and‐release programmes in the face of a threatening pathogen, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1002/ece3.73513openalex-snapshot
Field Survey of Freshwater Invertebrates Reveals That Several Groups Are Potential Carriers of the Fungal Pathogen Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1002/ece3.73767openalex-snapshot
Disease, Drought, and Warming: A Triple Threat to a Declining High‐Elevation Amphibian
inferred← citeshttps://doi.org/10.1002/edn3.283openalex-snapshot
Tracking the prevalence of a fungal pathogen, Batrachochytrium dendrobatidis (chytrid fungus), using environmental DNA
inferred← citeshttps://doi.org/10.1002/edn3.427openalex-snapshot
Large‐scale eDNA monitoring of multiple aquatic pathogens as a tool to provide risk maps for wildlife diseases
inferred← citeshttps://doi.org/10.1002/edn3.70051openalex-snapshot
Experimental Evidence of Rapidly Decaying Environmental DNA Highlights Infection Risk from Two Major Amphibian Pathogens
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/10.1002/jat.4050openalex-snapshot
How to disinfect anuran eggs? Sensitivity of anuran embryos to chemicals widely used for the disinfection of larval and post‐metamorphic amphibians
inferred← citeshttps://doi.org/10.1002/zoo.21154openalex-snapshot
Detection of pathogenic Batrachochytrium dendrobatidis using water filtration, animal and bait testing
inferred← citeshttps://doi.org/10.1007/s00027-026-01287-2openalex-snapshot
Drivers of aquatic zoosporic parasites in natural and artificial environments
inferred← citeshttps://doi.org/10.1007/s00248-006-9173-2openalex-snapshot
A Molecular Comparison of Plumage and Soil Bacteria Across Biogeographic, Ecological, and Taxonomic Scales
inferred← citeshttps://doi.org/10.1007/s00285-025-02252-7openalex-snapshot
Learned behavioral avoidance can alter outbreak dynamics in a model for waterborne infectious diseases
inferred← citeshttps://doi.org/10.1007/s00442-018-4167-6openalex-snapshot
Beyond the swab: ecosystem sampling to understand the persistence of an amphibian pathogen
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/s10344-024-01838-8openalex-snapshot
Assessing functional connectivity and anthropogenic impacts on Ambystoma altamirani populations in Bosque De Agua, Central Mexico
inferred← citeshttps://doi.org/10.1007/s10393-006-0075-zopenalex-snapshot
Experimental Infection and Repeat Survey Data Indicate the Amphibian Chytrid Batrachochytrium dendrobatidis May Not Occur on Freshwater Crustaceans in Northern Queensland, Australia
inferred← citeshttps://doi.org/10.1007/s10393-008-0154-4openalex-snapshot
Presence of the Chytrid Fungus Batrachochytrium dendrobatidis in Populations of the Critically Endangered Frog Mannophryne olmonae in Tobago, West Indies
inferred← citeshttps://doi.org/10.1007/s10393-008-0190-0openalex-snapshot
Chytridiomycosis and Amphibian Population Declines Continue to Spread Eastward in Panama
inferred← citeshttps://doi.org/10.1007/s10393-009-0227-zopenalex-snapshot
Tool for Estimating the Risk of Anthropogenic Spread of Batrachochytrium denrobatidis Between Water Bodies
inferred← citeshttps://doi.org/10.1007/s10393-010-0278-1openalex-snapshot
How Does Chytrid Infection Vary Among Habitats? The Case of Litoria wilcoxii (Anura, Hylidae) in SE Queensland, Australia
inferred← citeshttps://doi.org/10.1007/s10393-010-0313-2openalex-snapshot
Raising Awareness of Amphibian Chytridiomycosis will not Alienate Ecotourists Visiting Madagascar
inferred← citeshttps://doi.org/10.1007/s10393-010-0358-2openalex-snapshot
What Drives Chytrid Infections in Newt Populations? Associations with Substrate, Temperature, and Shade
inferred← citeshttps://doi.org/10.1007/s10393-016-1101-4openalex-snapshot
Prevalence and Seasonality of the Amphibian Chytrid Fungus Batrachochytrium dendrobatidis Along Widely Separated Longitudes Across the United States
inferred← citeshttps://doi.org/10.1007/s10393-017-1278-1openalex-snapshot
Batrachochytrium salamandrivorans and the Risk of a Second Amphibian Pandemic
inferred← citeshttps://doi.org/10.1007/s10393-020-01501-zopenalex-snapshot
Differences in Fungal Disease Dynamics in Co-occurring Terrestrial and Aquatic Amphibians
inferred← citeshttps://doi.org/10.1007/s10393-021-01566-4openalex-snapshot
The Last South American Redoubt? Tested Surinamese Anurans Still Chytrid Free
inferred← citeshttps://doi.org/10.1007/s10453-015-9374-6openalex-snapshot
Presence of amphibian chytrid fungus (Batrachochytrium dendrobatidis) in rainwater suggests aerial dispersal is possible
inferred← citeshttps://doi.org/10.1007/s10530-019-02041-6openalex-snapshot
The invasive red swamp crayfish (Procambarus clarkii) increases infection of the amphibian chytrid fungus (Batrachochytrium dendrobatidis)
inferred← citeshttps://doi.org/10.1007/s10530-020-02218-4openalex-snapshot
Effects of invasive larval bullfrogs (Rana catesbeiana) on disease transmission, growth and survival in the larvae of native amphibians
inferred← citeshttps://doi.org/10.1007/s10530-024-03304-7openalex-snapshot
Niche overlap by invasion of Oncorhynchus mykiss on the habitat of its amphibian prey in central Mexico
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/s10750-023-05218-2openalex-snapshot
Chytrid in the clouds: an alternative passive transport of a lethal pathogen for amphibians
inferred← citeshttps://doi.org/10.1007/s12041-017-0823-6openalex-snapshot
Genetic variability and structure of an isolated population of Ambystoma altamirani, a mole salamander that lives in the mountains of one of the largest urban areas in the world
inferred← citeshttps://doi.org/10.1007/s13199-025-01087-6openalex-snapshot
Fungi; friend or foe of amphibians
inferred← citeshttps://doi.org/10.1016/b978-1-4377-1986-4.00028-7openalex-snapshot
Diagnosis and Control of Amphibian Chytridiomycosis
inferred← citeshttps://doi.org/10.1016/b978-141604047-7.50020-8openalex-snapshot
Amphibian Chytridiomycosis
inferred← citeshttps://doi.org/10.1016/j.biocon.2015.12.041openalex-snapshot
In-situ itraconazole treatment improves survival rate during an amphibian chytridiomycosis epidemic
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.05.032openalex-snapshot
Living with the enemy: Facilitating amphibian coexistence with disease
inferred← citeshttps://doi.org/10.1016/j.biocon.2020.108521openalex-snapshot
Synergistic effects of warming and disease linked to high mortality in cool-adapted terrestrial frogs
inferred← citeshttps://doi.org/10.1016/j.cvex.2020.01.003openalex-snapshot
Selected Emerging Infectious Diseases of Amphibians
inferred← citeshttps://doi.org/10.1016/j.fbr.2007.02.002openalex-snapshot
The relationship between the emergence of Batrachochytrium dendrobatidis, the international trade in amphibians and introduced amphibian species
inferred← citeshttps://doi.org/10.1016/j.fbr.2008.02.001openalex-snapshot
The ecology of chytrids in aquatic ecosystems: roles in food web dynamics
inferred← citeshttps://doi.org/10.1016/j.funbio.2013.01.004openalex-snapshot
Combining ethidium monoazide treatment with real-time PCR selectively quantifies viable Batrachochytrium dendrobatidis cells
inferred← citeshttps://doi.org/10.1016/j.funeco.2008.12.002openalex-snapshot
Structure and function of fungal zoospores: ecological implications
inferred← citeshttps://doi.org/10.1016/j.gecco.2025.e03599openalex-snapshot
Reproductive habitat mismatch influences chytrid infection dynamics in a tropical amphibian community
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.scitotenv.2021.152735openalex-snapshot
The role of abiotic variables in an emerging global amphibian fungal disease in mountains
inferred← citeshttps://doi.org/10.1016/j.tree.2009.07.011openalex-snapshot
The ecology and impact of chytridiomycosis: an emerging disease of amphibians
inferred← citeshttps://doi.org/10.1017/9781316479964.018openalex-snapshot
When chytrid fungus invades: integrating theory and data to understand disease-induced amphibian declines
inferred← citeshttps://doi.org/10.1038/srep08633openalex-snapshot
Widespread presence of the pathogenic fungus Batrachochytrium dendrobatidis in wild amphibian communities in Madagascar
inferred← citeshttps://doi.org/10.1053/j.jepm.2015.06.013openalex-snapshot
Chytridiomycosis in Amphibians
inferred← citeshttps://doi.org/10.1071/wr14183openalex-snapshot
Using site-occupancy models to prepare for the spread of chytridiomyosis and identify factors affecting detectability of a cryptic susceptible species, the Tasmanian tree frog
inferred← citeshttps://doi.org/10.1073/pnas.0506889103openalex-snapshot
Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community
inferred← citeshttps://doi.org/10.1073/pnas.0600293103openalex-snapshot
Amphibian diversity: Decimation by disease
inferred← citeshttps://doi.org/10.1073/pnas.1200592110openalex-snapshot
Chytrid fungus Batrachochytrium dendrobatidis has nonamphibian hosts and releases chemicals that cause pathology in the absence of infection
inferred← citeshttps://doi.org/10.1079/cabicompendium.109124openalex-snapshot
Batrachochytrium dendrobatidis (Bd)
inferred← citeshttps://doi.org/10.1080/03014223.2010.548073openalex-snapshot
A survey for the amphibian chytrid fungus Batrachochytrium dendrobatidis in New Zealand's endemic Hochstetter's frog ( Leiopelma hochstetteri )
inferred← citeshttps://doi.org/10.1080/11250003.2012.753473openalex-snapshot
The pandemic pathogen of amphibians, Batrachochytrium dendrobatidis (Phylum Chytridiomycota), in Italy
inferred← citeshttps://doi.org/10.1080/23766808.2016.1151133openalex-snapshot
Rainbow trout (Oncorhynchus mykiss) threaten Andean amphibians
inferred← citeshttps://doi.org/10.1093/femspd/ftw069openalex-snapshot
Effects of chytridiomycosis on hematopoietic tissue in the spleen, kidney and bone marrow in three diverse amphibian species
inferred← citeshttps://doi.org/10.1093/icb/icae058openalex-snapshot
What Can Frogs Teach Us about Resilience? Adaptive Renewal in Amphibian and Academic Ecosystems
inferred← citeshttps://doi.org/10.1093/ismeco/ycaf185openalex-snapshot
Double-edged effects of aquatic environmental biofilms on Batrachochytrium dendrobatidis growth and inhibition
inferred← citeshttps://doi.org/10.1093/ismejo/wrae189openalex-snapshot
Biofilms inactivate the free-living stage of Batrachochytrium dendrobatidis, the most destructive pathogen for vertebrate diversity
inferred← citeshttps://doi.org/10.1098/rspb.2013.2783openalex-snapshot
Assessing host extinction risk following exposure to Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1098/rspb.2015.0694openalex-snapshot
Condition-dependent reproductive effort in frogs infected by a widespread pathogen
inferred← citeshttps://doi.org/10.1098/rspb.2023.2658openalex-snapshot
Invasibility of a North American soil ecosystem to amphibian-killing fungal pathogens
inferred← citeshttps://doi.org/10.1098/rstb.2012.0011openalex-snapshot
Ecophysiology meets conservation: understanding the role of disease in amphibian population declines
inferred← citeshttps://doi.org/10.1098/rstb.2022.0133openalex-snapshot
Amphibian infection tolerance to chytridiomycosis
inferred← citeshttps://doi.org/10.1111/1365-2435.70444openalex-snapshot
Fungal Batrachochytrium dendrobatidis infections proliferate during amphibian terrestrial dormancy
inferred← citeshttps://doi.org/10.1111/1365-2656.70282openalex-snapshot
Playing it safe at early life stages: Balancing energy allocations to maximize fitness under seasonal pathogen dynamics
inferred← citeshttps://doi.org/10.1111/1365-2664.12091openalex-snapshot
Do global models predicting environmental suitability for the amphibian fungus, B atrachochytrium dendrobatidis, have local value to conservation managers?
inferred← citeshttps://doi.org/10.1111/1758-2229.13274openalex-snapshot
The impacts of water quality on the amphibian chytrid fungal pathogen: A systematic review
inferred← citeshttps://doi.org/10.1111/acv.12665openalex-snapshot
Indirect terrestrial transmission of amphibian chytrid fungus from reservoir to susceptible host species leads to fatal chytridiomycosis
inferred← citeshttps://doi.org/10.1111/aec.13468openalex-snapshot
Don't take my trees: Re‐evaluating the importance of trees when it comes to managing green and golden bell frog, Litoria aurea, habitat
inferred← citeshttps://doi.org/10.1111/cobi.12143openalex-snapshot
The Threat of Disease Increases as Species Move Toward Extinction
inferred← citeshttps://doi.org/10.1111/cobi.12281openalex-snapshot
Environmental Determinants of Recent Endemism of Batrachochytrium dendrobatidis Infections in Amphibian Assemblages in the Absence of Disease Outbreaks
inferred← citeshttps://doi.org/10.1111/csp2.70022openalex-snapshot
Cool‐season environmental water delivery increases extinction risk for chytrid‐infected amphibians
inferred← citeshttps://doi.org/10.1111/ecog.00360openalex-snapshot
Distribution of the disease pathogen Batrachochytrium dendrobatidis in non‐epidemic amphibian communities of western Canada
inferred← citeshttps://doi.org/10.1111/ele.12463openalex-snapshot
Refugia and connectivity sustain amphibian metapopulations afflicted by disease
inferred← citeshttps://doi.org/10.1111/j.1600-0587.2009.05994.xopenalex-snapshot
Landscape epidemiology of Batrachochytrium dendrobatidis in central California
inferred← citeshttps://doi.org/10.1111/j.1748-1090.2007.00010.xopenalex-snapshot
Amphibian chytridiomycosis: strategies for captive management and conservation
inferred← citeshttps://doi.org/10.1111/jzo.12773openalex-snapshot
Chytrid fungus dynamics and infections associated with movement distances in a red‐listed amphibian
inferred← citeshttps://doi.org/10.1111/oik.03462openalex-snapshot
Initiation of Batrachochytrium dendrobatidis infection in the absence of physical contact with infected hosts – a field study in a high altitude lake
inferred← citeshttps://doi.org/10.1111/tbed.13568openalex-snapshot
Genetic analysis of post‐epizootic amphibian chytrid strains in Bolivia: Adding a piece to the puzzle
inferred← citeshttps://doi.org/10.11144/javeriana.10554.2026openalex-snapshot
Detección de Batrachochytrium dendrobatidis en el ensamblaje de anfibios en la Región Andina Central, Oriental, Orinoquia y Amazonia de Colombia y el estudio in-vitro de la accion antagonica de la bacteria Janthinobacterium lividum frente a la cepa colombiana de Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1128/9781555819453.ch21openalex-snapshot
The Emerging Amphibian Fungal Disease, Chytridiomycosis:A Key Example of the Global Phenomenon of Wildlife Emerging Infectious Diseases
inferred← citeshttps://doi.org/10.1128/iai.00035-19openalex-snapshot
Metabolites Involved in Immune Evasion by Batrachochytrium dendrobatidis Include the Polyamine Spermidine
inferred← citeshttps://doi.org/10.1128/microbiolspec.ei10-0004-2015openalex-snapshot
The Emerging Amphibian Fungal Disease, Chytridiomycosis: A Key Example of the Global Phenomenon of Wildlife Emerging Infectious Diseases
inferred← citeshttps://doi.org/10.1163/15685381-00003100openalex-snapshot
Low infection prevalence of the amphibian chytrid fungus Batrachochytrium dendrobatidis (Chytridiomycetes: Rhizophydiales) in Cuba
inferred← citeshttps://doi.org/10.1163/15685381-bja10183openalex-snapshot
Alien amphibian introductions via the plant trade: a breeding population of the Catalonian midwife toad (Alytes almogavarii) in Central Spain
inferred← citeshttps://doi.org/10.1186/1472-6785-10-6openalex-snapshot
Prevalence of the pathogenic chytrid fungus, Batrachochytrium dendrobatidis, in an endangered population of northern leopard frogs, Rana pipiens
inferred← citeshttps://doi.org/10.1186/s13567-015-0266-0openalex-snapshot
Amphibian chytridiomycosis: a review with focus on fungus-host interactions
inferred← citeshttps://doi.org/10.1201/ebk1420064162-c2openalex-snapshot
Declines and the Global Status of Amphibians
inferred← citeshttps://doi.org/10.12681/jhvms.15647openalex-snapshot
First detection of the amphibian chytrid fungus (Batrachochytridium dendrobatidis) in free- living anuran populations in Greece
inferred← citeshttps://doi.org/10.13001/uwnpsrc.2018.5663openalex-snapshot
Factors influencing amphibian distributions in Grand Teton National Park and western Wyoming
inferred← citeshttps://doi.org/10.1371/journal.pone.0016708openalex-snapshot
Seasonal Pattern of Batrachochytrium dendrobatidis Infection and Mortality in Lithobates areolatus: Affirmation of Vredenburg's “10,000 Zoospore Rule”
inferred← citeshttps://doi.org/10.1371/journal.pone.0022211openalex-snapshot
Do Frogs Get Their Kicks on Route 66? Continental U.S. Transect Reveals Spatial and Temporal Patterns of Batrachochytrium dendrobatidis Infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0035038openalex-snapshot
Waterfowl: Potential Environmental Reservoirs of the Chytrid Fungus Batrachochytrium dendrobatidis
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.0061061openalex-snapshot
Whether the Weather Drives Patterns of Endemic Amphibian Chytridiomycosis: A Pathogen Proliferation Approach
inferred← citeshttps://doi.org/10.1371/journal.pone.0069591openalex-snapshot
Spatial Assessment of Amphibian Chytrid Fungus (Batrachochytrium dendrobatidis) in South Africa Confirms Endemic and Widespread Infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0082425openalex-snapshot
Elevation, Temperature, and Aquatic Connectivity All Influence the Infection Dynamics of the Amphibian Chytrid Fungus in Adult Frogs
inferred← citeshttps://doi.org/10.1371/journal.pone.0086437openalex-snapshot
Comparison of the White-Nose Syndrome Agent Pseudogymnoascus destructans to Cave-Dwelling Relatives Suggests Reduced Saprotrophic Enzyme Activity
inferred← citeshttps://doi.org/10.1371/journal.pone.0090750openalex-snapshot
First Evidence of Amphibian Chytrid Fungus (Batrachochytrium dendrobatidis) and Ranavirus in Hong Kong Amphibian Trade
inferred← citeshttps://doi.org/10.1371/journal.pone.0106790openalex-snapshot
Heterogeneous Occupancy and Density Estimates of the Pathogenic Fungus Batrachochytrium dendrobatidis in Waters of North America
inferred← citeshttps://doi.org/10.1371/journal.pone.0125386openalex-snapshot
Terrestrial Dispersal and Potential Environmental Transmission of the Amphibian Chytrid Fungus (Batrachochytrium dendrobatidis)
inferred← citeshttps://doi.org/10.1371/journal.pone.0127851openalex-snapshot
Seasonal Ecology and Behavior of an Endangered Rainforest Frog (Litoria rheocola) Threatened by Disease
inferred← citeshttps://doi.org/10.1371/journal.pone.0155745openalex-snapshot
Spread of Amphibian Chytrid Fungus across Lowland Populations of Túngara Frogs in Panamá
inferred← citeshttps://doi.org/10.1371/journal.pone.0197710openalex-snapshot
Pathogen invasion and non-epizootic dynamics in Pacific newts in California over the last century
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
inferred← citeshttps://doi.org/10.1371/journal.pone.0199852openalex-snapshot
Effects of host species and environmental factors on the prevalence of Batrachochytrium dendrobatidis in northern Europe
inferred← citeshttps://doi.org/10.1371/journal.pone.0307833openalex-snapshot
Drosophila melanogaster as a model arthropod carrier for the amphibian chytrid fungus Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1638/2012-0219r.1openalex-snapshot
EFFICACY OF TREATMENT AND LONG-TERM FOLLOW-UP OFBATRACHOCHYTRIUM DENDROBATIDISPCR-POSITIVE ANURANS FOLLOWING ITRACONAZOLE BATH TREATMENT
inferred← citeshttps://doi.org/10.1643/ch-08-180openalex-snapshot
An Aquatic Disease on a Terrestrial Salamander: Individual and Population Level Effects of the Amphibian Chytrid Fungus, Batrachochytrium dendrobatidis, on Batrachoseps attenuatus (Plethodontidae)
inferred← citeshttps://doi.org/10.1890/08-2319.1openalex-snapshot
Using occupancy models to understand the distribution of an amphibian pathogen, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1890/es14-00263.1openalex-snapshot
Canopy cover and drought influence the landscape epidemiology of an amphibian chytrid fungus
inferred← citeshttps://doi.org/10.1894/0038-4909-57.3.323openalex-snapshot
The Chytrid FungusBatrachochytrium dendrobatidisin Isolated Populations of the Baja California TreefrogPseudacris hypochondriaca curtain Baja California Sur, mexico
inferred← citeshttps://doi.org/10.19136/era.a9n2.3300openalex-snapshot
Micobiota en la piel de anuros de la cuenca del río Coatán, Chiapas, México
inferred← citeshttps://doi.org/10.20506/rst.32.2.2210openalex-snapshot
Chytridiomycosis: a global threat to amphibians
inferred← citeshttps://doi.org/10.2110/palo.2011.p11-076ropenalex-snapshot
FIRST REPORT OF FUNGI AND FUNGUS-LIKE ORGANISMS FROM MESOZOIC HOT SPRINGS
inferred← citeshttps://doi.org/10.21829/azm.2019.3502066openalex-snapshot
Factores abióticos y bióticos determinantes para la presencia de Batrachochytrium dendrobatidis en anfibios mexicanos
inferred← citeshttps://doi.org/10.21892/9786287515383.10openalex-snapshot
Una revisión de la biología de Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.22201/fc.25942158e.2019.1.74openalex-snapshot
Ecología y evolución de enfermedades emergentes en anfibios: una revisión de ranavirus y quitridiomicosis
inferred← citeshttps://doi.org/10.22201/fc.25942158e.2020.1.93openalex-snapshot
DETECCIÓN DE Batrachochytrium dendrobatidis (CHYTRIDIOMYCOTA) EN LOCALIDADES DEL VALLE DEL CAUCA POR TÉCNICA DE PCR
inferred← citeshttps://doi.org/10.25148/etd.fidc009207openalex-snapshot
Back from the Brink?: Rebounding and Remnant Amphibian Populations in a Pathogen Enzootic Environment
inferred← citeshttps://doi.org/10.25560/4278openalex-snapshot
EXTINCTION RISK AND POPULATION DECLINES IN AMPHIBIANS
inferred← citeshttps://doi.org/10.25903/e8th-8151openalex-snapshot
Epidemiology of chytridiomycosis in rainforest stream tadpoles
inferred← citeshttps://doi.org/10.25903/psc7-z392openalex-snapshot
Why does Chytridiomycosis drive some frog populations to extinction and not others?: the effects of interspecific variation in host behaviour
inferred← citeshttps://doi.org/10.26686/wgtn.16968808openalex-snapshot
Returning an Endemic Frog to the New Zealand Mainland: Transfer and Adaptive Management of Leiopelma pakeka at Karori Sanctuary, Wellington
inferred← citeshttps://doi.org/10.26686/wgtn.16968808.v1openalex-snapshot
Returning an Endemic Frog to the New Zealand Mainland: Transfer and Adaptive Management of Leiopelma pakeka at Karori Sanctuary, Wellington
inferred← citeshttps://doi.org/10.2903/j.efsa.2018.5259openalex-snapshot
Risk of survival, establishment and spread of Batrachochytrium salamandrivorans (Bsal) in the EU
inferred← citeshttps://doi.org/10.3201/eid1093.120707openalex-snapshot
Parallels in Amphibian and Bat Declines from Pathogenic Fungi
inferred← citeshttps://doi.org/10.3201/eid1903.120707openalex-snapshot
Parallels in Amphibian and Bat Declines from Pathogenic Fungi
inferred← citeshttps://doi.org/10.3354/dao01850openalex-snapshot
Environmental detection of Batrachochytrium dendrobatidis in a temperate climate
inferred← citeshttps://doi.org/10.3354/dao01958openalex-snapshot
Infection intensity and sampling locality affectBatrachochytrium dendrobatidisdistribution among body regions on green-eyed tree frogsLitoria genimaculata
inferred← citeshttps://doi.org/10.3354/dao01975openalex-snapshot
Survival of the amphibian chytrid fungus Batrachochytrium dendrobatidis on bare hands and gloves: hygiene implications for amphibian handling
inferred← citeshttps://doi.org/10.3354/dao02006openalex-snapshot
First report of spontaneous chytridiomycosis in frogs in Asia
inferred← citeshttps://doi.org/10.3354/dao02026openalex-snapshot
Experimental infection of North American plethodontid salamanders with the fungus Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.3354/dao02212openalex-snapshot
Distribution and risk factors for spread of amphibian chytrid fungus Batrachochytrium dendrobatidis in the Tasmanian Wilderness World Heritage Area, Australia
inferred← citeshttps://doi.org/10.3354/dao02409openalex-snapshot
Reptiles as potential vectors and hosts of the amphibian pathogen Batrachochytrium dendrobatidis in Panama
inferred← citeshttps://doi.org/10.3354/dao02557openalex-snapshot
Batrachochytrium dendrobatidis in amphibians of Cameroon, including first records for caecilians
inferred← citeshttps://doi.org/10.3354/dao02778openalex-snapshot
Pathogenic fungus Batrachochytrium dendrobatidis in marbled water frog Telmatobius marmoratus: first record from Lake Titicaca, Bolivia
inferred← citeshttps://doi.org/10.3354/dao02810openalex-snapshot
Batrachochytrium dendrobatidis exposure effects on foraging efficiencies and body size in anuran tadpoles
inferred← citeshttps://doi.org/10.3354/dao02837openalex-snapshot
Amphibian pathogens at northern latitudes: presence of chytrid fungus and ranavirus in northeastern Canada
inferred← citeshttps://doi.org/10.3354/dao02934openalex-snapshot
Delayed metamorphosis of amphibian larvae facilitates Batrachochytrium dendrobatidis transmission and persistence
inferred← citeshttps://doi.org/10.3354/dao03045openalex-snapshot
Jumping into a trap: high prevalence of chytrid fungus in the preferred microhabitats of a bromeliad-specialist frog
inferred← citeshttps://doi.org/10.3354/dao03046openalex-snapshot
Seasonal infection rates of Batrachochytrium dendrobatidis in populations of northern green frog Lithobates clamitans melanota tadpoles
inferred← citeshttps://doi.org/10.3354/dao03160openalex-snapshot
Detection of amphibian chytrid fungus on waterfowl integument in natural settings
inferred← citeshttps://doi.org/10.3354/dao03191openalex-snapshot
Amphibian chytrid infection is influenced by rainfall seasonality and water availability
inferred← citeshttps://doi.org/10.3354/dao03278openalex-snapshot
Age- and size-dependent resistance to chytridiomycosis in the invasive cane toad Rhinella marina
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/dao03712openalex-snapshot
Infectious disease threats to amphibians in Greece: new localities positive for Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.3354/dao03905openalex-snapshot
Cost-effective DNA extraction method for detection of amphibian fungal pathogen in invertebrate samples
inferred← citeshttps://doi.org/10.3354/dao074007openalex-snapshot
Retreat sites of rain forest stream frogs are not a reservoir for Batrachochytrium dendrobatidis in northern Queensland, Australia
inferred← citeshttps://doi.org/10.3354/dao074013openalex-snapshot
Additional disinfectants effective against the amphibian chytrid fungus Batrachochytrium dendrobatidis
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/10.3390/d10040124openalex-snapshot
The Biogeography of Great Salt Lake Halophilic Archaea: Testing the Hypothesis of Avian Mechanical Carriers
inferred← citeshttps://doi.org/10.3390/pathogens12030429openalex-snapshot
Major Emerging Fungal Diseases of Reptiles and Amphibians
inferred← citeshttps://doi.org/10.3390/su9020280openalex-snapshot
Indirect Consequences of Recreational Fishing in Freshwater Ecosystems: An Exploration from an Australian Perspective
inferred← citeshttps://doi.org/10.35513/21658005.2019.1.5openalex-snapshot
Mosquitoes as a potential vector for the transmission of the amphibian chytrid fungus
inferred← citeshttps://doi.org/10.35537/10915/26403openalex-snapshot
Susceptibilidad y sensibilidad de algunas especies de anuros a la infección por el hongo Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.3897/arphapreprints.e68571openalex-snapshot
Third time’s the charm: The definitive rediscovery of Telmatobius halli Noble, 1938 (Anura, Telmatobiidae) at its historic type locality
inferred← citeshttps://doi.org/10.3897/herpetozoa.32.e38023openalex-snapshot
Genetic diversity and structure of two endangered mole salamander species of the Trans-Mexican Volcanic Belt
inferred← citeshttps://doi.org/10.3897/zookeys.1079.69036openalex-snapshot
The definitive rediscovery of Telmatobius halli (Anura, Telmatobiidae) at its historic type locality and its synonymy with T. dankoi and T. vilamensis
inferred← citeshttps://doi.org/10.4013/nbc.2017.121.04openalex-snapshot
Amphibian trade and the presence of Batrachochytrium dendrobatidis in free-ranging: dispersion in vicious circle?
inferred← citeshttps://doi.org/10.47749/t/unicamp.2019.1161992openalex-snapshot
Modelo matemático do triângulo Anuros - Ambiente - Bd
inferred← citeshttps://doi.org/10.47749/t/unicamp.2020.1255609openalex-snapshot
Effect of spatial scale in biotic and abiotic factors in the distribution of the chytrid fungus in the Atlantic Forest
inferred← citeshttps://doi.org/10.47749/t/unicamp.2022.1258819openalex-snapshot
Transport of a lethal amphibian pathogen (Batrachochytrium dendrobatidis) through fog
inferred← citeshttps://doi.org/10.5167/uzh-24664openalex-snapshot
Desinfektion als Massnahme gegen die Verbreitung der Chytridiomykose bei Amphibien
inferred← citeshttps://doi.org/10.5818/jhms-d-23-00001openalex-snapshot
Report on the First Global Amphibian and Reptile Disease (GARD) Conference 2022
inferred← citeshttps://doi.org/10.5852/naturae2024a14openalex-snapshot
Biosécurité en milieu humide : bonnes pratiques d’intervention sur les amphibiens sauvages
inferred← citeshttps://doi.org/10.5860/choice.187931openalex-snapshot
Relicts of a beautiful sea: survival, extinction, and conservation in a desert world
inferred← citeshttps://doi.org/10.70675/954f4915ze33ez457aza4d8z2a1b19c2e768openalex-snapshot
Abiotic variables in disease expression of a fungal pathogen in mountains under global change
inferred← citeshttps://doi.org/10.70675/dc2da72cz6e7dz4328z87d9zf99f251dc12dopenalex-snapshot
Déclin et inventaire de la biodiversité : les maladies des amphibiens et la méthode de l'ADN environnemental
inferred← citeshttps://doi.org/10.7282/t36t0n20openalex-snapshot
Evidence of endocrine disruption in amphibians due to agricultural chemical exposure
inferred← citeshttps://doi.org/10.7282/t3hh6k7copenalex-snapshot
An assessment of the correlation between amphibian populations, chytridiomycete communities, and the ecological integrity of the habitat
inferred← citeshttps://doi.org/10.7589/0090-3558-43.1.48openalex-snapshot
SURVEILLANCE FOR BATRACHOCHYTRIUM DENDROBATIDIS USING MIXOPHYES (ANURA: MYOBATRACHIDAE) LARVAE
inferred← citeshttps://doi.org/10.7589/0090-3558-45.4.1198openalex-snapshot
Distribution Limits of Batrachochytrium dendrobatidis: A Case Study in the Rocky Mountains, USA
inferred← citeshttps://doi.org/10.7589/2016-04-074openalex-snapshot
Detection of the Amphibian Chytrid FungusBatrachochytrium dendrobatidisin Museum Specimens of Andean Aquatic Birds: Implications for Pathogen Dispersal
inferred← citeshttps://doi.org/10.7589/2016-07-172openalex-snapshot
Evidence of Batrachochytrium dendrobatidis Infection in Amphibians from Serbian Lowlands
inferred← citeshttps://doi.org/10.7589/2019-08-212openalex-snapshot
Detection of the Amphibian Pathogens Chytrid Fungus (Batrachochytrium dendrobatidis) and Ranavirus in West Texas, USA, Using Environmental DNA
inferred← citeshttps://doi.org/10.7589/jwd-d-24-00094openalex-snapshot
Evaluating the Efficacy of Disinfectant Methods Against Emydomyces testavorans, a Fungus Associated with Shell Disease in Freshwater Aquatic Turtles
inferred← citeshttps://doi.org/10.7717/peerj.4698openalex-snapshot
Seasonal migrations, body temperature fluctuations, and infection dynamics in adult amphibians
inferred← citeshttps://doi.org/10.7717/peerj.7021openalex-snapshot
Reservoir frogs: seasonality of Batrachochytrium dendrobatidis infection in robber frogs in Dominica and Montserrat
inferred← citeshttps://doi.org/10.7882/az.2008.012openalex-snapshot
Do Green and Golden Bell Frogs Litoria aurea occupy habitats with fungicidal properties?
inferred← citeshttps://doi.org/10.7882/az.2008.015openalex-snapshot
The impact of the Amphibian Chytrid Fungus Batrachochytrium dendrobatidis on a Green and Golden Bell Frog Litoria aurea reintroduction program at the Hunter Wetlands Centre Australia in the Hunter Region of NSW
inferred← citeshttps://doi.org/10.82308/31090openalex-snapshot
Persistence and prevalence of the enzootic chytrid fungus, «Batrachochytrium dendrobatidis», in relation to amphibian population decline in Panama
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