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Improving breed‐and‐release programmes in the face of a threatening pathogen, Batrachochytrium dendrobatidis

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What this work says

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

inferredcites →https://doi.org/10.1002/9781444355833.ch1openalex-snapshot

Animal Translocations: What are they and why do we do them?

inferredcites →https://doi.org/10.1007/bf00222519openalex-snapshot

Amphibians: suitable candidates for breeding-release programmes

inferredcites →https://doi.org/10.1007/s00442-014-3157-6openalex-snapshot

Evidence of a salt refuge: chytrid infection loads are suppressed in hosts exposed to salt

inferredcites →https://doi.org/10.1007/s00442-016-3607-4openalex-snapshot

Susceptibility to disease varies with ontogeny and immunocompetence in a threatened amphibian

inferredcites →https://doi.org/10.1007/s10393-007-0093-5openalex-snapshot

Spread of Chytridiomycosis Has Caused the Rapid Global Decline and Extinction of Frogs

inferredcites →https://doi.org/10.1007/s10393-010-0327-9openalex-snapshot

Persistence with Chytridiomycosis Does Not Assure Survival of Direct-developing Frogs

inferredcites →https://doi.org/10.1007/s10453-015-9374-6openalex-snapshot

Presence of amphibian chytrid fungus (Batrachochytrium dendrobatidis) in rainwater suggests aerial dispersal is possible

inferredcites →https://doi.org/10.1007/s13157-010-0029-7openalex-snapshot

Rapid Turnover in Site Occupancy of a Pond-breeding Frog Demonstrates the Need for Landscape-level Management

inferredcites →https://doi.org/10.1016/0169-5347(91)90048-3openalex-snapshot

Infectious diseases of humans: Dynamics and control

inferredcites →https://doi.org/10.1016/j.biocel.2011.12.002openalex-snapshot

Frog skin epithelium: Electrolyte transport and chytridiomycosis

inferredcites →https://doi.org/10.1016/j.biocon.2005.10.046openalex-snapshot

Year-round distribution of white-chinned petrels from South Georgia: Relationships with oceanography and fisheries

inferredcites →https://doi.org/10.1016/j.biocon.2015.08.010openalex-snapshot

Factors driving the distribution of an endangered amphibian toward an industrial landscape in Australia

inferredcites →https://doi.org/10.1016/s0006-3207(02)00040-xopenalex-snapshot

Management of freshwater wetlands for the endangered green and golden bell frog ( Litoria aurea ): roles of habitat determinants and space

inferredcites →https://doi.org/10.1017/s0030605307001767openalex-snapshot

The reintroduction of large carnivores to the Eastern Cape, South Africa: an assessment

inferredcites →https://doi.org/10.1017/s0962728600005637openalex-snapshot

Guidelines for reintroductions and other conservation translocations

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/10.1071/wr16145openalex-snapshot

Assessing host response to disease treatment: how chytrid-susceptible frogs react to increased water salinity

inferredcites →https://doi.org/10.1071/wr9930687openalex-snapshot

The Importance of Disease in Reintroduction Programmes.

inferredcites →https://doi.org/10.1071/zo06093openalex-snapshot

Life history of an endangered amphibian challenges the declining species paradigm

inferredcites →https://doi.org/10.1073/pnas.0912886107openalex-snapshot

Enzootic and epizootic dynamics of the chytrid fungal pathogen of amphibians

inferredcites →https://doi.org/10.1080/15572536.2005.11832990openalex-snapshot

Physiology ofBatrachochytrium dendrobatidis, a chytrid pathogen of amphibians

inferredcites →https://doi.org/10.1083/jcb.200611141openalex-snapshot

Error bars in experimental biology

inferredcites →https://doi.org/10.1093/femsle/fnw111openalex-snapshot

Low disease-causing threshold in a frog species susceptible to chytridiomycosis

inferredcites →https://doi.org/10.1098/rsbl.2015.0874openalex-snapshot

Successful elimination of a lethal wildlife infectious disease in nature

inferredcites →https://doi.org/10.1098/rspb.1997.0202openalex-snapshot

The effect of cowpox virus infection on fecundity in bank voles and wood mice

inferredcites →https://doi.org/10.1111/1365-2664.13030openalex-snapshot

Elevated salinity blocks pathogen transmission and improves host survival from the global amphibian chytrid pandemic: Implications for translocations

inferredcites →https://doi.org/10.1111/acv.12230openalex-snapshot

Chytrid infection and post-release fitness in the reintroduction of an endangered alpine tree frog

inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00298.xopenalex-snapshot

PATTERNS OF NATURAL SELECTION ON SIZE AT METAMORPHOSIS IN WATER FROGS

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.1365-2486.2010.02272.xopenalex-snapshot

Climate change, chytridiomycosis or condition: an experimental test of amphibian survival

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.2012.05481.xopenalex-snapshot

Only skin deep: shared genetic response to the deadly chytrid fungus in susceptible frog species

inferredcites →https://doi.org/10.1111/j.1442-9993.2012.02452.xopenalex-snapshot

Life stage specific variation in the occupancy of ponds by L itoria aurea, a threatened amphibian

inferredcites →https://doi.org/10.1111/j.1461-0248.2004.00693.xopenalex-snapshot

Mechanisms of disease‐induced extinction

inferredcites →https://doi.org/10.1111/j.1469-1795.2010.00407.xopenalex-snapshot

Host species determines whether infection load increases beyond disease‐causing thresholds following exposure to the amphibian chytrid fungus

inferredcites →https://doi.org/10.1111/j.1469-7998.2006.00220.xopenalex-snapshot

Large‐scale seasonal variation in the prevalence and severity of chytridiomycosis

inferredcites →https://doi.org/10.1111/j.1523-1739.1988.tb00336.xopenalex-snapshot

Disease and Endangered Species: The Black‐footed Ferret as a Recent Example

inferredcites →https://doi.org/10.1111/j.1523-1739.2008.00967.xopenalex-snapshot

Captive Breeding, Reintroduction, and the Conservation of Amphibians

inferredcites →https://doi.org/10.1111/j.1523-1739.2008.01123.xopenalex-snapshot

Suitability of Amphibians and Reptiles for Translocation

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.1600-0587.2009.05968.xopenalex-snapshot

U‐CARE: Utilities for performing goodness of fit tests and manipulating CApture–REcapture data

inferredcites →https://doi.org/10.1111/j.1600-065x.1998.tb01265.xopenalex-snapshot

Metamorphosis and the amphibian immune system

inferredcites →https://doi.org/10.1111/j.1751-0813.2004.tb11137.xopenalex-snapshot

Effect of season and temperature on mortality in amphibians due to chytridiomycosis

inferredcites →https://doi.org/10.1111/j.2007.0030-1299.15863.xopenalex-snapshot

Host‐parasite population dynamics under combined frequency‐ and density‐dependent transmission

inferredcites →https://doi.org/10.1126/science.1103538openalex-snapshot

Status and Trends of Amphibian Declines and Extinctions Worldwide

inferredcites →https://doi.org/10.1136/thx.47.12.1060openalex-snapshot

Use of jet mixing devices with an oxygen concentrator.

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/10.1242/jeb.040865openalex-snapshot

The cause of global amphibian declines: a developmental endocrinologist's perspective

inferredcites →https://doi.org/10.1371/journal.pone.0026215openalex-snapshot

Short-Term Exposure to Warm Microhabitats Could Explain Amphibian Persistence with Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.1371/journal.pone.0028444openalex-snapshot

Nothing a Hot Bath Won't Cure: Infection Rates of Amphibian Chytrid Fungus Correlate Negatively with Water Temperature under Natural Field Settings

inferredcites →https://doi.org/10.1371/journal.pone.0033567openalex-snapshot

A Reservoir Species for the Emerging Amphibian Pathogen Batrachochytrium dendrobatidis Thrives in a Landscape Decimated by Disease

inferredcites →https://doi.org/10.1371/journal.pone.0035038openalex-snapshot

Waterfowl: Potential Environmental Reservoirs of the Chytrid Fungus Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.1371/journal.pone.0036942openalex-snapshot

Sodium Chloride Inhibits the Growth and Infective Capacity of the Amphibian Chytrid Fungus and Increases Host Survival Rates

inferredcites →https://doi.org/10.1371/journal.pone.0143629openalex-snapshot

Dynamics of Chytridiomycosis during the Breeding Season in an Australian Alpine Amphibian

inferredcites →https://doi.org/10.1371/journal.pone.0159143openalex-snapshot

We Made Your Bed, Why Won’t You Lie in It? Food Availability and Disease May Affect Reproductive Output of Reintroduced Frogs

inferredcites →https://doi.org/10.1670/07-0862.1openalex-snapshot

Movement Patterns of Adult Green and Golden Bell Frogs Litoria aurea and the Implications for Conservation Management

inferredcites →https://doi.org/10.1890/06-1842.1openalex-snapshot

LIFE-HISTORY TRADE-OFFS INFLUENCE DISEASE IN CHANGING CLIMATES: STRATEGIES OF AN AMPHIBIAN PATHOGEN

inferredcites →https://doi.org/10.1890/12-1270.1openalex-snapshot

Context‐dependent amphibian host population response to an invading pathogen

inferredcites →https://doi.org/10.1890/13-0389.1openalex-snapshot

Wetland characteristics influence disease risk for a threatened amphibian

inferredcites →https://doi.org/10.2307/1521041openalex-snapshot

Successful Reintroduction of the Yellow-Crowned Night-Heron as a Nesting Resident on Bermuda

inferredcites →https://doi.org/10.2307/1938295openalex-snapshot

Factors Affecting Population Fluctuations in Larval and Adult Stages of the Wood Frog (Rana Sylvatica)

inferredcites →https://doi.org/10.2307/3545585openalex-snapshot

Estimating Fitness: A Comparison of Body Condition Indices

inferredcites →https://doi.org/10.2307/5339openalex-snapshot

Regulation and Stability of a Free-Living Host-Parasite System: Trichostrongylus tenuis in Red Grouse. II. Population Models

inferredcites →https://doi.org/10.2460/javma.1986.189.01.22openalex-snapshot

Sampling for detection of infection or disease in animal populations

inferredcites →https://doi.org/10.3201/eid0908.030145openalex-snapshot

Survival ofBatrachochytrium dendrobatidisin Water: Quarantine and Disease Control Implications

inferredcites →https://doi.org/10.32800/abc.2005.28.0189openalex-snapshot

Principles and interest of GOF tests for multistate capture-recapture models

inferredcites →https://doi.org/10.3354/cr00878openalex-snapshot

Contrasting effects of environmental factors during larval stage on morphological plasticity in post-metamorphic frogs

inferredcites →https://doi.org/10.3354/dao01830openalex-snapshot

Behaviour of Australian rainforest stream frogs may affect the transmission of chytridiomycosis

inferredcites →https://doi.org/10.3354/dao01923openalex-snapshot

Survey protocol for detecting chytridiomycosis in all Australian frog populations

inferredcites →https://doi.org/10.3354/dao02103openalex-snapshot

Yellow band disease compromises the reproductive output of the Caribbean reef-building coral Montastraea faveolata (Anthozoa, Scleractinia)

inferredcites →https://doi.org/10.3354/dao02118openalex-snapshot

Presence of the amphibian chytrid fungus Batrachochytrium dendrobatidis in threatened corroboree frog populations in the Australian Alps

inferredcites →https://doi.org/10.3354/dao02336openalex-snapshot

Temperature, hydric environment, and prior pathogen exposure alter the experimental severity of chytridiomycosis in boreal toads

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/dao065181openalex-snapshot

Possible modes of dissemination of the amphibian chytrid Batrachochytrium dendrobatidis in the environment

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

Diagnostic assays and sampling protocols for the detection of Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.5860/choice.32-0304openalex-snapshot

Measuring and monitoring biological diversity: standard methods for amphibians

inferredcites →https://doi.org/10.7882/az.1996.010openalex-snapshot

Distribution and conservation status of the Green and Golden Bell Frog Litoria aurea in New South Wales

inferredcites →https://doi.org/10.7882/az.2001.003openalex-snapshot

A Review of the Biology of the Green and Golden Bell Frog Litoria aurea

inferredcites →https://doi.org/10.7882/az.2008.001openalex-snapshot

An olympic legacy: Green and golden bell frog conservation at Sydney Olympic Park 1993-2006

inferredcites →https://doi.org/10.7882/az.2008.002openalex-snapshot

Frogs on the hop: translocations of Green and Golden Bell Frogs Litoria aurea in Greater Sydney

inferredcites →https://doi.org/10.7882/az.2008.003openalex-snapshot

Reintroduction of the Green and Golden Bell Frog Litoria aurea to Pambula on the south coast of New South Wales

inferredcites →https://doi.org/10.7882/az.2008.009openalex-snapshot

Impact of a Chytrid-related mortality event on a population of the Green and Golden Bell Frog Litoria aurea

inferredcites →https://doi.org/10.7882/az.2008.012openalex-snapshot

Do Green and Golden Bell Frogs Litoria aurea occupy habitats with fungicidal properties?

inferredcites →https://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

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.4795486openalex-extracted

Understanding and Predicting Disease Dynamics for an Endangered Amphibian Using Long-Term Surveys of Wild and Translocated Frogs

inferred← citeshttps://doi.org/10.1002/eap.3085openalex-snapshot

Differential recruitment drives pathogen‐mediated competition between species in an amphibian chytridiomycosis system

inferred← citeshttps://doi.org/10.1038/s44358-025-00101-5openalex-snapshot

Conservation priorities for global amphibian biodiversity

inferred← citeshttps://doi.org/10.1098/rstb.2024.0333openalex-snapshot

Managing populations after a disease outbreak: exploration of epidemiological consequences of managed host reintroduction following disease-driven host decline

inferred← citeshttps://doi.org/10.3390/ani13101634openalex-snapshot

Complex Organisms Must Deal with Complex Threats: How Does Amphibian Conservation Deal with Biphasic Life Cycles?

inferred← citeshttps://doi.org/10.3390/ani13213379openalex-snapshot

Assessing Disease Risks in Wildlife Translocation Projects: A Comprehensive Review of Disease Incidents

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