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Seasonal variation of Batrachochytrium dendrobatidis in a threatened anuran species from Uruguay

https://doi.org/10.3354/dao03603
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-0-387-87458-6openalex-snapshot
Mixed effects models and extensions in ecology with R
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Linking global warming to amphibian declines through its effects on female body condition and survivorship
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Contrasting effects of temperature and precipitation change on amphibian phenology, abundance and performance
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Experimental Exposures of Boreal Toads (Bufo boreas) to a Pathogenic Chytrid Fungus (Batrachochytrium dendrobatidis)
inferredcites →https://doi.org/10.1007/s10393-009-0272-7openalex-snapshot
Impacts of Batrachochytrium dendrobatidis Infection on Tadpole Foraging Performance
inferredcites →https://doi.org/10.1007/s10393-013-0833-7openalex-snapshot
Fitness Consequences of Infection by Batrachochytrium dendrobatidis in Northern Leopard Frogs (Lithobates pipiens)
inferredcites →https://doi.org/10.1016/j.cvfa.2003.11.006openalex-snapshot
Reproductive consequences of infection with bovine viral diarrhea virus
inferredcites →https://doi.org/10.1016/j.funeco.2020.100995openalex-snapshot
Biotic and abiotic determinants of Batrachochytrium dendrobatidis infections in amphibians of the Brazilian Atlantic Forest
inferredcites →https://doi.org/10.1016/j.gecco.2019.e00551openalex-snapshot
Impact of seasonal cycles on host-pathogen dynamics and disease mitigation for Batrachochytrium salamandrivorans
inferredcites →https://doi.org/10.1038/38483openalex-snapshot
Trade-off between parasitoid resistance and larval competitive ability in Drosophila melanogaster
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Warming drives ecological community changes linked to host-associated microbiome dysbiosis
inferredcites →https://doi.org/10.1038/s41598-017-16425-yopenalex-snapshot
Low resistance to chytridiomycosis in direct-developing amphibians
inferredcites →https://doi.org/10.1038/s41598-018-22002-8openalex-snapshot
Body size influences energetic and osmoregulatory costs in frogs infected with Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1038/s41598-018-35874-7openalex-snapshot
Interaction between temperature and sublethal infection with the amphibian chytrid fungus impacts a susceptible frog species
inferredcites →https://doi.org/10.1038/s41598-020-62351-xopenalex-snapshot
Host density and habitat structure influence host contact rates and Batrachochytrium salamandrivorans transmission
inferredcites →https://doi.org/10.1038/srep01515openalex-snapshot
Hot bodies protect amphibians against chytrid infection in nature
inferredcites →https://doi.org/10.1038/srep10828openalex-snapshot
Host species vary in infection probability, sub-lethal effects and costs of immune response when exposed to an amphibian parasite
inferredcites →https://doi.org/10.1046/j.1365-2656.2003.00777.xopenalex-snapshot
The population dynamical implications of covert infections in host–microparasite interactions
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.0912886107openalex-snapshot
Enzootic and epizootic dynamics of the chytrid fungal pathogen of amphibians
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.1200592110openalex-snapshot
Chytrid fungus Batrachochytrium dendrobatidis has nonamphibian hosts and releases chemicals that cause pathology in the absence of infection
inferredcites →https://doi.org/10.1080/00275514.1999.12061011openalex-snapshot
Batrachochytrium dendrobatidis gen. et sp. nov., a chytrid pathogenic to amphibians
inferredcites →https://doi.org/10.1080/01650521.2017.1364952openalex-snapshot
Reproductive biology ofMelanophryniscus montevidensis(Anura: Bufonidae) from Uruguay: reproductive effort, fecundity, sex ratio and sexual size dimorphism
inferredcites →https://doi.org/10.1086/346134openalex-snapshot
Assessing the Cost of Mounting an Immune Response
inferredcites →https://doi.org/10.1098/rspb.1999.0650openalex-snapshot
Cost of resistance: relationship between reduced fertility and increased resistance in a snail—schistosome host—parasite system
inferredcites →https://doi.org/10.1098/rspb.2014.1796openalex-snapshot
Partitioning the net effect of host diversity on an emerging amphibian pathogen
inferredcites →https://doi.org/10.1111/1365-2435.12370openalex-snapshot
Skin sloughing rate increases with chytrid fungus infection load in a susceptible amphibian
inferredcites →https://doi.org/10.1111/2041-210x.13361openalex-snapshot
Systematic review of modelling assumptions and empirical evidence: Does parasite transmission increase nonlinearly with host density?
inferredcites →https://doi.org/10.1111/btp.12928openalex-snapshot
Midges not only sucks, but may carry lethal pathogens to wild amphibians
inferredcites →https://doi.org/10.1111/eva.12520openalex-snapshot
Amphibian species traits, evolutionary history and environment predict Batrachochytrium dendrobatidis infection patterns, but not extinction risk
inferredcites →https://doi.org/10.1111/j.1365-2435.2006.01163.xopenalex-snapshot
Immune challenge reduces reproductive output and growth in a lizard
inferredcites →https://doi.org/10.1111/j.1365-2656.2007.01256.xopenalex-snapshot
Quantifying the disease transmission function: effects of density onBatrachochytrium dendrobatidistransmission in the mountain yellow‐legged frogRana muscosa
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.1461-0248.2005.00879.xopenalex-snapshot
Seasonality and the dynamics of infectious diseases
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.1600-0587.2012.07348.xopenalex-snapshot
Collinearity: a review of methods to deal with it and a simulation study evaluating their performance
inferredcites →https://doi.org/10.1111/j.1600-0706.2008.16783.xopenalex-snapshot
Testing a key assumption of host‐pathogen theory: density and disease transmission
inferredcites →https://doi.org/10.1111/j.1600-0706.2009.17643.xopenalex-snapshot
New perspectives for estimating body condition from mass/length data: the scaled mass index as an alternative method
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/10.1126/science.1059026openalex-snapshot
Population Biology of Multihost Pathogens
inferredcites →https://doi.org/10.1126/science.aao0500openalex-snapshot
Amphibians on the brink
inferredcites →https://doi.org/10.1126/science.aav0379openalex-snapshot
Amphibian fungal panzootic causes catastrophic and ongoing loss of biodiversity
inferredcites →https://doi.org/10.1139/cjz-2017-0362openalex-snapshot
Seasonal demography of the threatened Montevideo Redbelly Toad (Melanophryniscus montevidensis) in a protected area of Uruguay
inferredcites →https://doi.org/10.1152/physrev.1991.71.1.93openalex-snapshot
Fever: Role of Pyrogens and Cryogens
inferredcites →https://doi.org/10.11606/issn.2316-9079.v12i2p97-106openalex-snapshot
Potential Effects of Climate Change on the Distribution of an Endangered Species: Melanophryniscus montevidensis (Anura: Bufonidae)
inferredcites →https://doi.org/10.1163/156853807781374818openalex-snapshot
Effects of a paved road on mortality and mobility of red bellied toads (Melanophryniscus sp.) in Argentinean grasslands
inferredcites →https://doi.org/10.1186/s13567-015-0266-0openalex-snapshot
Amphibian chytridiomycosis: a review with focus on fungus-host interactions
inferredcites →https://doi.org/10.1242/jeb.167445openalex-snapshot
A pathogenic skin fungus and sloughing exacerbate cutaneous water loss in amphibians
inferredcites →https://doi.org/10.1371/journal.pone.0008408openalex-snapshot
Expression Profiling the Temperature-Dependent Amphibian Response to Infection by Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1371/journal.pone.0056802openalex-snapshot
Mapping the Global Emergence of Batrachochytrium dendrobatidis, the Amphibian Chytrid Fungus
inferredcites →https://doi.org/10.1371/journal.pone.0062146openalex-snapshot
Host Stress Response Is Important for the Pathogenesis of the Deadly Amphibian Disease, Chytridiomycosis, in Litoria caerulea
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.0082425openalex-snapshot
Elevation, Temperature, and Aquatic Connectivity All Influence the Infection Dynamics of the Amphibian Chytrid Fungus in Adult Frogs
inferredcites →https://doi.org/10.1371/journal.pone.0094625openalex-snapshot
Climate Change and the Distribution of Neotropical Red-Bellied Toads (Melanophryniscus, Anura, Amphibia): How to Prioritize Species and Populations?
inferredcites →https://doi.org/10.1371/journal.pone.0130554openalex-snapshot
Seasonal Variation in Population Abundance and Chytrid Infection in Stream-Dwelling Frogs of the Brazilian Atlantic Forest
inferredcites →https://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
inferredcites →https://doi.org/10.1371/journal.pone.0242913openalex-snapshot
Significant reductions of host abundance weakly impact infection intensity of Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1655/herpetologica-d-15-00013openalex-snapshot
Seasonality, Environmental Factors, and Host Behavior Linked to Disease Risk in Stream-Dwelling Tadpoles
inferredcites →https://doi.org/10.18637/jss.v067.i01openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.2108/zs150077openalex-snapshot
Use of Reproductive Microhabitat byMelanophryniscus montevidensis(Anura: Bufonidae) from Uruguay
inferredcites →https://doi.org/10.22201/fc.25942158e.2019.2.76openalex-snapshot
ANURANS FROM BARRA DE LA LAGUNA DE ROCHA (ROCHA, URUGUAY)
inferredcites →https://doi.org/10.2307/5220openalex-snapshot
The Effects of a Sublethal Baculovirus Infection in the Indian Meal Moth, Plodia interpunctella
inferredcites →https://doi.org/10.2994/sajh-d-15-00020.1openalex-snapshot
Movement Patterns in a Uruguayan Population ofMelanophryniscus montevidensis(Philippi, 1902) (Anura: Bufonidae) Using Photo-Identification for Individual Recognition
inferredcites →https://doi.org/10.3354/dao01838openalex-snapshot
Electrolyte depletion and osmotic imbalance in amphibians with chytridiomycosis
inferredcites →https://doi.org/10.3354/dao02035openalex-snapshot
Chytridiomycosis in frogs from Uruguay
inferredcites →https://doi.org/10.3354/dao02054openalex-snapshot
Seasonality of Batrachochytrium dendrobatidis infection in direct-developing frogs suggests a mechanism for persistence
inferredcites →https://doi.org/10.3354/dao02337openalex-snapshot
Elevated temperature as a treatment for Batrachochytrium dendrobatidis infection in captive frogs
inferredcites →https://doi.org/10.3354/dao02940openalex-snapshot
Physiological responses of Brazilian amphibians to an enzootic infection of the chytrid fungus Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.3354/dao03191openalex-snapshot
Amphibian chytrid infection is influenced by rainfall seasonality and water availability
inferredcites →https://doi.org/10.3354/dao055065openalex-snapshot
Emerging disease of amphibians cured by elevated body temperature
inferredcites →https://doi.org/10.3354/dao060141openalex-snapshot
Rapid quantitative detection of chytridiomycosis (Batrachochytrium dendrobatidis) in amphibian samples using real-time Taqman PCR assay
inferredcites →https://doi.org/10.3354/dao068047openalex-snapshot
Virulence of the amphibian chytrid fungus Batrachochytrium dendrobatidis varies with the strain
inferredcites →https://doi.org/10.3354/dao068051openalex-snapshot
Life cycle stages of the amphibian chytrid Batrachochytrium dendrobatidis
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/10.3354/dao075201openalex-snapshot
Strain differences in the amphibian chytrid Batrachochytrium dendrobatidis and non-permanent, sub-lethal effects of infection
inferredcites →https://doi.org/10.4322/natcon.2012.026openalex-snapshot
Identification of priority areas for conservation of two endangered parapatric species of red-bellied toads using ecological niche models and hotspot analysis
inferredcites →https://doi.org/10.7717/peerj.5891openalex-snapshot
Novel findings on the impact of chytridiomycosis on the cardiac function of anurans: sensitive vs. tolerant species

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

inferred← citeshttps://doi.org/10.5281/zenodo.15271642zenodo-depositor-declared
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.pecon.2025.07.001openalex-snapshot
Climatic driver of chytrid prevalence in the Critically Endangered Admirable Redbelly Toad
inferred← citeshttps://doi.org/10.1038/s41598-025-97367-8openalex-snapshot
Host and environmental factors drive prevalence of the pathogen Batrachochytrium dendrobatidis in Central African amphibians
inferred← citeshttps://doi.org/10.1111/1462-2920.70131openalex-snapshot
Skin Bacteriome Structure and Batrachochytrium dendrobatidis Prevalence Differs Amongst Two Sympatric Salamanders in the San Francisco Bay Area
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4281618/v1openalex-snapshot
Climatic drivers of chytrid prevalence in the critically endangered Admirable Redbelly Toad
inferred← citeshttps://doi.org/10.3354/dao03783openalex-snapshot
Widespread occurrence of the amphibian chytrid panzootic lineage in Uruguay is constrained by climate
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