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Thermal Physiology, Disease, and Amphibian Declines on the Eastern Slopes of the Andes
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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.1791openalex-snapshot
Spatio‐temporal rainfall variability in the Amazon basin countries (Brazil, Peru, Bolivia, Colombia, and Ecuador)
inferredcites →https://doi.org/10.1007/978-94-015-1252-7_5openalex-snapshot
20th Century Climate Change in the Tropical Andes: Observations and Model Results
inferredcites →https://doi.org/10.1007/bf00329034openalex-snapshot
Implications of microhabitat selection and patterns of activity on the thermal ecology of high elevation neotropical anurans
inferredcites →https://doi.org/10.1007/s00704-004-0045-8openalex-snapshot
Interdecadal variability and trends of rainfall across the Amazon basin
inferredcites →https://doi.org/10.1007/s00704-012-0687-xopenalex-snapshot
Enhanced temperature variability in high-altitude climate change
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.2008.04.014openalex-snapshot
Decline and extirpation of an endangered Panamanian stream frog population (Craugastor punctariolus) due to an outbreak of chytridiomycosis
inferredcites →https://doi.org/10.1016/j.cbpa.2006.04.035openalex-snapshot
Physiological basis for diurnal activity in dispersing juvenile Bufo granulosus in the Caatinga, a Brazilian semi-arid environment
inferredcites →https://doi.org/10.1016/j.earscirev.2008.04.002openalex-snapshot
Climate change and tropical Andean glaciers: Past, present and future
inferredcites →https://doi.org/10.1016/s0306-4565(97)00065-xopenalex-snapshot
Thermal extremes at high elevations in the Andes: Physiological ecology of frogs
inferredcites →https://doi.org/10.1023/a:1024406427519openalex-snapshot
20th Century Climate Change in the Tropical Andes: Observations and Model Results
inferredcites →https://doi.org/10.1029/2000gl011871openalex-snapshot
Mean annual temperature trends and their vertical structure in the tropical Andes
inferredcites →https://doi.org/10.1029/2000jd900134openalex-snapshot
Interannual climate variability in the Central Andes and its relation to tropical Pacific and Atlantic forcing
inferredcites →https://doi.org/10.1029/2002jd002473openalex-snapshot
Optical properties of the Indo‐Asian haze layer over the tropical Indian Ocean
inferredcites →https://doi.org/10.1029/2002jd002959openalex-snapshot
Tropical climate change recorded by a glacier in the central Andes during the last decades of the twentieth century: Chacaltaya, Bolivia, 16°S
inferredcites →https://doi.org/10.1029/2008jd011021openalex-snapshot
Climate change projections for the tropical Andes using a regional climate model: Temperature and precipitation simulations for the end of the 21st century
inferredcites →https://doi.org/10.1029/2012jd017789openalex-snapshot
Cloud frequency climatology at the Andes/Amazon transition: 2. Trends and variability
inferredcites →https://doi.org/10.1038/416389aopenalex-snapshot
Ecological responses to recent climate change
inferredcites →https://doi.org/10.1038/nature04246openalex-snapshot
Widespread amphibian extinctions from epidemic disease driven by global warming
inferredcites →https://doi.org/10.1038/nature09407openalex-snapshot
Global metabolic impacts of recent climate warming
inferredcites →https://doi.org/10.1038/nature10947openalex-snapshot
Emerging fungal threats to animal, plant and ecosystem health
inferredcites →https://doi.org/10.1038/srep01515openalex-snapshot
Hot bodies protect amphibians against chytrid infection in nature
inferredcites →https://doi.org/10.1046/j.1461-0248.2003.00387.xopenalex-snapshot
Temperature checks the Red Queen? Resistance and virulence in a fluctuating environment
inferredcites →https://doi.org/10.1073/pnas.0506889103openalex-snapshot
Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community
inferredcites →https://doi.org/10.1073/pnas.0709472105openalex-snapshot
Impacts of climate warming on terrestrial ectotherms across latitude
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.0808913106openalex-snapshot
The potential for behavioral thermoregulation to buffer “cold-blooded” animals against climate warming
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.0914115107openalex-snapshot
Epidemic disease decimates amphibian abundance, species diversity, and evolutionary history in the highlands of central Panama
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/10.1080/15572536.2005.11832990openalex-snapshot
Physiology ofBatrachochytrium dendrobatidis, a chytrid pathogen of amphibians
inferredcites →https://doi.org/10.1086/285141openalex-snapshot
Physiological Consequences of Habitat Selection
inferredcites →https://doi.org/10.1086/285573openalex-snapshot
Evaluating Temperature Regulation by Field-Active Ectotherms: The Fallacy of the Inappropriate Question
inferredcites →https://doi.org/10.1086/physzool.69.6.30164271openalex-snapshot
Metabolic Physiology, Locomotor Performance, and Thermal Niche Breadth in Neotropical Anurans
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/10.1098/rspb.2008.1957openalex-snapshot
Why tropical forest lizards are vulnerable to climate warming
inferredcites →https://doi.org/10.1098/rstb.2012.0005openalex-snapshot
Predicting organismal vulnerability to climate warming: roles of behaviour, physiology and adaptation
inferredcites →https://doi.org/10.1111/j.1365-2435.2006.01159.xopenalex-snapshot
Negative effects of changing temperature on amphibian immunity under field conditions
inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01682.xopenalex-snapshot
Dry spots and wet spots in the Andean hotspot
inferredcites →https://doi.org/10.1111/j.1461-0248.2009.01434.xopenalex-snapshot
Factors driving pathogenicity vs. prevalence of amphibian panzootic chytridiomycosis in Iberia
inferredcites →https://doi.org/10.1111/j.1523-1739.1998.96359.xopenalex-snapshot
Decline of a Tropical Montane Amphibian Fauna
inferredcites →https://doi.org/10.1111/j.1523-1739.2005.00255.xopenalex-snapshot
The Novel and Endemic Pathogen Hypotheses: Competing Explanations for the Origin of Emerging Infectious Diseases of Wildlife
inferredcites →https://doi.org/10.1111/j.1523-1739.2010.01572.xopenalex-snapshot
Constraints to Species’ Elevational Range Shifts as Climate Changes
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.1523-1739.2011.01667.xopenalex-snapshot
Temperature Constraint of Elevational Range of Tropical Amphibians: Response to Forero‐Medina et al.
inferredcites →https://doi.org/10.1111/j.1744-7429.2005.00025.xopenalex-snapshot
Cambios en la Diversidad en Siete Comunidades de Anuros en los Andes de Ecuador1
inferredcites →https://doi.org/10.1111/j.1744-7429.2005.00026.xopenalex-snapshot
Catastrophic Population Declines and Extinctions in Neotropical Harlequin Frogs (Bufonidae: Atelopus ) 1
inferredcites →https://doi.org/10.1126/science.1103538openalex-snapshot
Status and Trends of Amphibian Declines and Extinctions Worldwide
inferredcites →https://doi.org/10.1126/science.1162547openalex-snapshot
Global Warming, Elevational Range Shifts, and Lowland Biotic Attrition in the Wet Tropics
inferredcites →https://doi.org/10.1126/science.122.3158.73openalex-snapshot
Acclimation of the Critical Thermal Maximum of the Reptile Urosaurus ornatus
inferredcites →https://doi.org/10.1128/mbio.00061-10openalex-snapshot
Global Warming Will Bring New Fungal Diseases for Mammals
inferredcites →https://doi.org/10.11606/issn.2316-9079.v8i2p147-148openalex-snapshot
Terrestrial-breeding frogs (Strabomantidae) in Peru
inferredcites →https://doi.org/10.1175/1520-0442(2001)014<2779:irvots>2.0.co;2openalex-snapshot
Interannual Rainfall Variability over the South American Altiplano
inferredcites →https://doi.org/10.1177/194008290800100406openalex-snapshot
Current State of Conservation Knowledge on Threatened Amphibian Species in Peru
inferredcites →https://doi.org/10.1186/1742-9994-8-8openalex-snapshot
Mitigating amphibian disease: strategies to maintain wild populations and control chytridiomycosis
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/10.1670/07-006.1openalex-snapshot
Plaster Models to Measure Operative Temperature and Evaporative Water Loss of Amphibians
inferredcites →https://doi.org/10.2307/1565080openalex-snapshot
Temporal Fluctuations in Abundances of Anuran Amphibians in a Seasonal Amazonian Rainforest
inferredcites →https://doi.org/10.2307/1565438openalex-snapshot
The Use of Agar Models to Study Amphibian Thermal Ecology
inferredcites →https://doi.org/10.2307/1565690openalex-snapshot
Thermal Dependency of Field Locomotor and Vocal Performance of High-Elevation Anurans in the Tropical Andes
inferredcites →https://doi.org/10.2307/1942256openalex-snapshot
A Model of the Dynamic Exchanges of Water and Energy between a Terrestrial Amphibian and Its Environment
inferredcites →https://doi.org/10.2307/3761981openalex-snapshot
Physiology of Batrachochytrium dendrobatidis, a Chytrid Pathogen of Amphibians
inferredcites →https://doi.org/10.3354/cr01127openalex-snapshot
Diurnal, seasonal, and altitudinal trends in microclimate across a tropical montane cloud forest
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/dao071149openalex-snapshot
Cost efficiency in the detection of chytridiomycosis using PCR assay
inferredcites →https://doi.org/10.3354/dao073175openalex-snapshot
Diagnostic assays and sampling protocols for the detection of Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.5194/tc-7-103-2013openalex-snapshot
Glacier changes and climate trends derived from multiple sources in the data scarce Cordillera Vilcanota region, southern Peruvian Andes
inferredcites →https://doi.org/10.5860/choice.49-6872openalex-snapshot
IUCN Red List of Threatened Species
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4394.2.2zenodo-depositor-declared
Pristimantis antisuyu sp. n. and Pristimantis erythroinguinis sp. n., two new species of terrestrial-breeding frogs (Anura, Strabomantidae) from the eastern slopes of the Andes in Manu National Park, Peru
inferred← citeshttps://doi.org/10.11646/zootaxa.4691.5.7zenodo-depositor-declared
Integrative taxonomy reveals first country record of Hyalinobatrachium mondolfii Señaris and Ayarzagüena 2001, and distribution range extensions for Cochranella nola Harvey 1996, and Rulyrana spiculata Duellman 1976 (Anura: Centrolenidae) in Peru
inferred← citeshttps://doi.org/10.1002/ece3.2779openalex-snapshot
Long‐term monitoring of tropical alpine habitat change, Andean anurans, and chytrid fungus in the Cordillera Vilcanota, Peru: Results from a decade of study
inferred← citeshttps://doi.org/10.1002/ece3.2929openalex-snapshot
Divergence of thermal physiological traits in terrestrial breeding frogs along a tropical elevational gradient
inferred← citeshttps://doi.org/10.1002/ece3.73944openalex-snapshot
Physiological and Skin Microbiome Divergence Among Closely Related Anurans Co‐Occurring in Agricultural Wetlands
inferred← citeshttps://doi.org/10.1002/ece3.7521openalex-snapshot
Environmental heterogeneity shapes physiological traits in tropical direct‐developing frogs
inferred← citeshttps://doi.org/10.1007/978-3-030-31167-4_27openalex-snapshot
Unexpected Beta-Diversity Radiations in Highland Clades of Andean Terraranae Frogs
inferred← citeshttps://doi.org/10.1007/978-981-10-3573-9_5openalex-snapshot
Climate Change and Biodiversity
inferred← citeshttps://doi.org/10.1007/s00248-017-0933-yopenalex-snapshot
Variation in Metabolite Profiles of Amphibian Skin Bacterial Communities Across Elevations in the Neotropics
inferred← citeshttps://doi.org/10.1007/s10393-016-1138-4openalex-snapshot
Detection of Batrachochytrium dendrobatidis in Amphibians Imported into the UK for the Pet Trade
inferred← citeshttps://doi.org/10.1007/s10393-016-1188-7openalex-snapshot
Survey of Pathogenic Chytrid Fungi (Batrachochytrium dendrobatidis and B. salamandrivorans) in Salamanders from Three Mountain Ranges in Europe and the Americas
inferred← citeshttps://doi.org/10.1007/s10393-021-01570-8openalex-snapshot
Three Pathogens Impact Terrestrial Frogs from a High-Elevation Tropical Hotspot
inferred← citeshttps://doi.org/10.1007/s10530-017-1390-8openalex-snapshot
Unraveling the historical prevalence of the invasive chytrid fungus in the Bolivian Andes: implications in recent amphibian declines
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.ecochg.2021.100041openalex-snapshot
Warming increases activity in the common tropical frog Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.1016/j.ecolind.2023.111100openalex-snapshot
Biodiversity responses to land-use change in the equatorial Andes
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2015.11.007openalex-snapshot
Density regulation in toad populations (Epidalea calamita, Bufotes viridis) by differential winter survival of juveniles
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2017.07.001openalex-snapshot
Modeling warming predicts a physiological threshold for the extinction of the living fossil frog Calyptocephalella gayi
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2021.103148openalex-snapshot
Response to thermal and hydric regimes point to differential inter- and intraspecific vulnerability of tropical amphibians to climate warming
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2024.103815openalex-snapshot
Thermal limits along tropical elevational gradients: Poison frog tadpoles show plasticity but maintain divergence across elevation
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/10.1038/s41586-025-08665-0openalex-snapshot
Vulnerability of amphibians to global warming
inferred← citeshttps://doi.org/10.1038/s41597-022-01704-9openalex-snapshot
A comprehensive database of amphibian heat tolerance
inferred← citeshttps://doi.org/10.1038/s41597-025-06286-wopenalex-snapshot
AmphiTherm: a comprehensive database of amphibian thermal tolerance and preference
inferred← citeshttps://doi.org/10.1038/s41598-017-09950-3openalex-snapshot
Infection increases vulnerability to climate change via effects on host thermal tolerance
inferred← citeshttps://doi.org/10.1073/pnas.1714891115openalex-snapshot
Phylogenetic homogenization of amphibian assemblages in human-altered habitats across the globe
inferred← citeshttps://doi.org/10.1073/pnas.2423706122openalex-snapshot
Thermal mismatch models derived from occurrence data predict pathogen prevalence in frogs
inferred← citeshttps://doi.org/10.1080/23766808.2019.1659022openalex-snapshot
Altitudinal differences in alpha, beta and functional diversity of an amphibian community in a biodiversity hotspot
inferred← citeshttps://doi.org/10.1086/725237openalex-snapshot
Shifts in the Thermal Dependence of Locomotor Performance across an Altitudinal Gradient in Native Populations of Xenopus laevis
inferred← citeshttps://doi.org/10.1093/iob/obad009openalex-snapshot
Beyond Janzen's Hypothesis: How Amphibians That Climb Tropical Mountains Respond to Climate Variation
inferred← citeshttps://doi.org/10.1111/1365-2656.13309openalex-snapshot
Thermal tolerance and the importance of microhabitats for Andean frogs in the context of land use and climate change
inferred← citeshttps://doi.org/10.1111/acv.12352openalex-snapshot
Cutaneous bacteria, but not peptides, are associated with chytridiomycosis resistance in Peruvian marsupial frogs
inferred← citeshttps://doi.org/10.1111/brv.12950openalex-snapshot
Impacts of anthropogenic climate change on tropical montane forests: an appraisal of the evidence
inferred← citeshttps://doi.org/10.1111/btp.12824openalex-snapshot
After the epizootic: Host–pathogen dynamics in montane tropical amphibian communities with high prevalence of chytridiomycosis
inferred← citeshttps://doi.org/10.1111/btp.12875openalex-snapshot
Thermal adaptations to extreme freeze–thaw cycles in the high tropical Andes
inferred← citeshttps://doi.org/10.1111/cobi.12769openalex-snapshot
Tropical amphibians in shifting thermal landscapes under land‐use and climate change
inferred← citeshttps://doi.org/10.1111/ecog.04226openalex-snapshot
Rethinking the scale and formulation of indices assessing organism vulnerability to warmer habitats
inferred← citeshttps://doi.org/10.1111/ele.12641openalex-snapshot
Infection risk decreases with increasing mismatch in host and pathogen environmental tolerances
inferred← citeshttps://doi.org/10.1111/ele.12901openalex-snapshot
Thermal biology mediates responses of amphibians and reptiles to habitat modification
inferred← citeshttps://doi.org/10.1111/eva.12520openalex-snapshot
Amphibian species traits, evolutionary history and environment predict Batrachochytrium dendrobatidis infection patterns, but not extinction risk
inferred← citeshttps://doi.org/10.1111/gcb.70275openalex-snapshot
Experimental Drought Suppresses Amphibian Pathogen Yet Intensifies Transmission and Disrupts Protective Skin Microbiome
inferred← citeshttps://doi.org/10.1111/geb.13069openalex-snapshot
No evidence for the ‘rate‐of‐living’ theory across the tetrapod tree of life
inferred← citeshttps://doi.org/10.1111/jbi.13596openalex-snapshot
Elevational and microclimatic drivers of thermal tolerance in Andean Pristimantis frogs
inferred← citeshttps://doi.org/10.1111/mec.13052openalex-snapshot
Mechanistic insights into landscape genetic structure of two tropical amphibians using field‐derived resistance surfaces
inferred← citeshttps://doi.org/10.1126/science.aav0379openalex-snapshot
Amphibian fungal panzootic causes catastrophic and ongoing loss of biodiversity
inferred← citeshttps://doi.org/10.1126/science.aax1682openalex-snapshot
A global perspective on tropical montane rivers
inferred← citeshttps://doi.org/10.1146/annurev-environ-102014-021358openalex-snapshot
State of the World's Amphibians
inferred← citeshttps://doi.org/10.11606/issn.2316-9079.v16i2p129-141openalex-snapshot
A new species of Bryophryne (Anura: Strabomantidae) from the Cordillera de Vilcabamba, southeastern Peruvian Andes
inferred← citeshttps://doi.org/10.1177/194008291500800304openalex-snapshot
A Re-Assessment of Priority Amphibian Species of Peru
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/10.1371/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.0145864openalex-snapshot
Co-Infection by Chytrid Fungus and Ranaviruses in Wild and Harvested Frogs in the Tropical Andes
inferred← citeshttps://doi.org/10.1371/journal.pone.0186478openalex-snapshot
Epizootic to enzootic transition of a fungal disease in tropical Andean frogs: Are surviving species still susceptible?
inferred← citeshttps://doi.org/10.1371/journal.pone.0219759openalex-snapshot
Thermal physiological traits in tropical lowland amphibians: Vulnerability to climate warming and cooling
inferred← citeshttps://doi.org/10.1371/journal.pone.0254439openalex-snapshot
Living with the pathogenic chytrid fungus: Exploring mechanisms of coexistence in the harlequin toad Atelopus cruciger
inferred← citeshttps://doi.org/10.15381/rpb.v26i4.16238openalex-snapshot
Revisión taxonómica de la rana marsupial Gastrotheca peruana (Amphibia: Hemiphractidae) en base al gen mitocondrial 16S
inferred← citeshttps://doi.org/10.18257/raccefyn.2655openalex-snapshot
Modulación metabólica a temperaturas crecientes: un enfoque ontogenético en la rana tropical de alta montaña Dendropsophus molitor (Hylidae)
inferred← citeshttps://doi.org/10.19227/jzar.v3i4.112openalex-snapshot
Itraconazole treatment of Batrachochytrium dendrobatidis (Bd) infection in captive caecilians (Amphibia: Gymnophiona) and the first case of Bd in a wild neotropical caecilian
inferred← citeshttps://doi.org/10.21315/tlsr2024.35.1.12openalex-snapshot
Thermal Relationship in Tropical Anurans from Two Contrasting Habitats Along an Elevation Gradient in Colombia
inferred← citeshttps://doi.org/10.22201/ib.20078706e.2021.92.3218openalex-snapshot
Pérdida de agua por evaporación en Gastrotheca marsupiata y Pleurodema cinereum en un valle seco altoandino
inferred← citeshttps://doi.org/10.25148/etd.fi14071193openalex-snapshot
Connectivity of fragmented amphibian populations in a Neotropical landscape
inferred← citeshttps://doi.org/10.25148/etd.fidc006988openalex-snapshot
Survival at the Summits: Amphibian Responses to Thermal Extremes, Disease, and Rapid Climate Change in the High Tropical Andes
inferred← citeshttps://doi.org/10.25148/etd.fidc008895openalex-snapshot
The Metabolic Ecology of Tropical Amphibians Across an Elevational Gradient in the Andes of Southeastern Peru
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/10.2994/sajh-d-18-00047.1openalex-snapshot
Climatic Heterogeneity in the Bolivian Andes: Are Frogs Trapped?
inferred← citeshttps://doi.org/10.3354/dao03094openalex-snapshot
Complex interactive effects of water mold, herbicide, and the fungus Batrachochytrium dendrobatidis on Pacific treefrog Hyliola regilla hosts
inferred← citeshttps://doi.org/10.3354/esr00831openalex-snapshot
Conservation physiology can inform threat assessment and recovery planning processes for threatened species
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/fmicb.2018.00465openalex-snapshot
Widespread Elevational Occurrence of Antifungal Bacteria in Andean Amphibians Decimated by Disease: A Complex Role for Skin Symbionts in Defense Against Chytridiomycosis
inferred← citeshttps://doi.org/10.3389/fvets.2021.728232openalex-snapshot
Tracking, Synthesizing, and Sharing Global Batrachochytrium Data at AmphibianDisease.org
inferred← citeshttps://doi.org/10.3390/ani13203162openalex-snapshot
Current State of Conservation Physiology for Amphibians: Major Research Topics and Physiological Parameters
inferred← citeshttps://doi.org/10.3390/d11090145openalex-snapshot
A New Species of Terrestrial-Breeding Frog (Amphibia, Strabomantidae, Noblella) from the Upper Madre De Dios Watershed, Amazonian Andes and Lowlands of Southern Peru
inferred← citeshttps://doi.org/10.3390/d12050184openalex-snapshot
A New Genus of Terrestrial-Breeding Frogs (Holoadeninae, Strabomantidae, Terrarana) from Southern Peru
inferred← citeshttps://doi.org/10.3390/land12010130openalex-snapshot
Phylogeny and Morphology Determine Vulnerability to Global Warming in Pristimantis Frogs
inferred← citeshttps://doi.org/10.3897/vz.71.e60097openalex-snapshot
A new species of marsupial frog (Anura; Gastrotheca) from the Cordillera de Colán in northeastern Peru
inferred← citeshttps://doi.org/10.3897/zookeys.1063.69580openalex-snapshot
Amphibians of the equatorial seasonally dry forests of Ecuador and Peru
inferred← citeshttps://doi.org/10.3897/zookeys.480.8578openalex-snapshot
A new species of Telmatobius (Amphibia, Anura, Telmatobiidae) from the Pacific slopes of the Andes, Peru
inferred← citeshttps://doi.org/10.3897/zookeys.516.9776openalex-snapshot
A new species of Noblella (Amphibia, Anura, Craugastoridae) from the humid montane forests of Cusco, Peru
inferred← citeshttps://doi.org/10.3897/zookeys.594.8295openalex-snapshot
A new species of Pristimantis (Amphibia, Anura, Craugastoridae) from the foothills of the Andes in Manu National Park, southeastern Peru
inferred← citeshttps://doi.org/10.3897/zookeys.685.12152openalex-snapshot
Bryophryne phuyuhampatu sp. n., a new species of Cusco Andes frog from the cloud forest of the eastern slopes of the Peruvian Andes (Amphibia, Anura, Craugastoridae)
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/10.7287/peerj.1807v0.1/reviews/1openalex-snapshot
Peer Review #1 of "A new species of Psychrophrynella (Amphibia, Anura, Craugastoridae) from the humid montane forests of Cusco, eastern slopes of the Peruvian Andes (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4313v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Evolutionary radiation of earless frogs in the Andes: molecular phylogenetics and habitat shifts in high-elevation terrestrial breeding frogs (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4313v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Evolutionary radiation of earless frogs in the Andes: molecular phylogenetics and habitat shifts in high-elevation terrestrial breeding frogs (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4444v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Psychrophrynella glauca sp. n., a new species of terrestrial-breeding frogs (Amphibia, Anura, Strabomantidae) from the montane forests of the Amazonian Andes of Puno, Peru (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4444v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Psychrophrynella glauca sp. n., a new species of terrestrial-breeding frogs (Amphibia, Anura, Strabomantidae) from the montane forests of the Amazonian Andes of Puno, Peru (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4444v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Psychrophrynella glauca sp. n., a new species of terrestrial-breeding frogs (Amphibia, Anura, Strabomantidae) from the montane forests of the Amazonian Andes of Puno, Peru (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4444v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Psychrophrynella glauca sp. n., a new species of terrestrial-breeding frogs (Amphibia, Anura, Strabomantidae) from the montane forests of the Amazonian Andes of Puno, Peru (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.6780v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Noblella thiuni sp. n., a new (singleton) species of minute terrestrial-breeding frog (Amphibia, Anura, Strabomantidae) from the montane forest of the Amazonian Andes of Puno, Peru (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6780v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Noblella thiuni sp. n., a new (singleton) species of minute terrestrial-breeding frog (Amphibia, Anura, Strabomantidae) from the montane forest of the Amazonian Andes of Puno, Peru (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6780v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Noblella thiuni sp. n., a new (singleton) species of minute terrestrial-breeding frog (Amphibia, Anura, Strabomantidae) from the montane forest of the Amazonian Andes of Puno, Peru (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.6780v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Noblella thiuni sp. n., a new (singleton) species of minute terrestrial-breeding frog (Amphibia, Anura, Strabomantidae) from the montane forest of the Amazonian Andes of Puno, Peru (v0.2)"
inferred← citeshttps://doi.org/10.7589/2015-02-052openalex-snapshot
Prevalence of Batrachochytrium dendrobatidis in Eastern Hellbender (Cryptobranchus alleganiensis) Populations in West Virginia, USA
inferred← citeshttps://doi.org/10.7589/jwd-d-20-00105openalex-snapshot
TEMPERATURE AS A DRIVER OF THE PATHOGENICITY AND VIRULENCE OF AMPHIBIAN CHYTRID FUNGUS BATRACHOCHYTRIUM DENDROBATIDIS: A SYSTEMATIC REVIEW
inferred← citeshttps://doi.org/10.7717/peerj.1807openalex-snapshot
A new species of Psychrophrynella (Amphibia, Anura, Craugastoridae) from the humid montane forests of Cusco, eastern slopes of the Peruvian Andes
inferred← citeshttps://doi.org/10.7717/peerj.20775openalex-snapshot
Effect of temperature acclimation period on upper thermal tolerance in a terrestrial salamander
inferred← citeshttps://doi.org/10.7717/peerj.4313openalex-snapshot
Evolutionary radiation of earless frogs in the Andes: molecular phylogenetics and habitat shifts in high-elevation terrestrial breeding frogs
inferred← citeshttps://doi.org/10.7717/peerj.4444openalex-snapshot
Psychrophrynella glauca sp. n., a new species of terrestrial-breeding frogs (Amphibia, Anura, Strabomantidae) from the montane forests of the Amazonian Andes of Puno, Peru
inferred← citeshttps://doi.org/10.7717/peerj.6780openalex-snapshot
Noblella thiuni sp. n., a new (singleton) species of minute terrestrial-breeding frog (Amphibia, Anura, Strabomantidae) from the montane forest of the Amazonian Andes of Puno, Peru
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