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

https://doi.org/10.1111/acv.12230
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What this work says

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

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Animal Translocations: What are they and why do we do them?
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Reintroduction of captive-born animals
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Spread of Chytridiomycosis Has Caused the Rapid Global Decline and Extinction of Frogs
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Relocation, repatriation, and translocation of amphibians and reptiles: are they conservation strategies that work?
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Effect of background color and low temperature on skin color and circulating α-MSH in two species of leopard frog
inferredcites →https://doi.org/10.1016/0169-5347(96)20092-8openalex-snapshot
Reintroduction: challenges and lessons for basic ecology
inferredcites →https://doi.org/10.1016/0300-9629(92)90164-lopenalex-snapshot
Growth rates and body condition factors of Alligator mississippiensis in coastal Louisiana wetlands: A comparison of wild and farm-released juveniles
inferredcites →https://doi.org/10.1016/j.biocon.2014.02.034openalex-snapshot
Animal reintroductions: An innovative assessment of survival
inferredcites →https://doi.org/10.1016/j.biocon.2014.11.032openalex-snapshot
Low impact of chytridiomycosis on frog recruitment enables persistence in refuges despite high adult mortality
inferredcites →https://doi.org/10.1016/j.tree.2007.10.003openalex-snapshot
Directions in reintroduction biology
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An assessment of the published results of animal relocations
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Mobility decisions and the predation risks of reintroduction
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A Recovery Program for the Natterjack Toad ( Bufo calamita ) in Britain
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Translocations of Amphibians: Proven Management Method or Experimental Technique?
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
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Susceptibility of amphibians to chytridiomycosis is associated with MHC class II conformation
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Taming wildlife disease: bridging the gap between science and management
inferredcites →https://doi.org/10.1111/cobi.12254openalex-snapshot
Understanding Publication Bias in Reintroduction Biology by Assessing Translocations of New Zealand's Herpetofauna
inferredcites →https://doi.org/10.1111/cobi.12322openalex-snapshot
Interventions for Reducing Extinction Risk in Chytridiomycosis‐Threatened Amphibians
inferredcites →https://doi.org/10.1111/j.1365-2907.2005.00070.xopenalex-snapshot
The effects of captivity on the morphology of captive, domesticated and feral mammals
inferredcites →https://doi.org/10.1111/j.1469-1795.2012.00536.xopenalex-snapshot
A brighter future for frogs? The influence of carotenoids on the health, development and reproductive success of the red‐eye tree frog
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.1526-100x.2010.00724.xopenalex-snapshot
From Reintroduction to Assisted Colonization: Moving along the Conservation Translocation Spectrum
inferredcites →https://doi.org/10.1111/j.1600-0706.2010.18845.xopenalex-snapshot
Amphibian phenotypic variation along a gradient in canopy cover: species differences and plasticity
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.245.4917.477openalex-snapshot
Translocation as a Species Conservation Tool: Status and Strategy
inferredcites →https://doi.org/10.1126/science.288.5468.985openalex-snapshot
Black-Footed Ferret Recovery
inferredcites →https://doi.org/10.1139/z03-036openalex-snapshot
Temperature and ontogenetic effects on color change in the larval salamander species Ambystoma barbouri and Ambystoma texanum
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.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/10.1643/cp-09-121openalex-snapshot
Overwintering Physiology and Hibernacula Microclimates of Blanchard's Cricket Frogs at Their Northwestern Range Boundary
inferredcites →https://doi.org/10.1890/0012-9658(2001)082[1473:mlrmob]2.0.co;2openalex-snapshot
MASS/LENGTH RESIDUALS: MEASURES OF BODY CONDITION OR GENERATORS OF SPURIOUS RESULTS?
inferredcites →https://doi.org/10.1890/0012-9658(2003)084[0391:osorla]2.0.co;2openalex-snapshot
OVERWINTER SURVIVAL OF RANA LESSONAE AND ITS HEMICLONAL ASSOCIATE RANA ESCULENTA
inferredcites →https://doi.org/10.2307/1936109openalex-snapshot
An Analysis of Background Color-Matching in Amphibians and Reptiles
inferredcites →https://doi.org/10.2307/1937827openalex-snapshot
Winterkill, Oxygen Relations, and Energy Metabolism of a Submerged Dormant Amphibian, Rana Muscosa
inferredcites →https://doi.org/10.2307/2290246openalex-snapshot
Practical Statistics for Medical Research.
inferredcites →https://doi.org/10.2307/3802403openalex-snapshot
Creative Conservation: Interactive Management of Wild and Captive Animals
inferredcites →https://doi.org/10.32800/abc.2004.27.0207openalex-snapshot
M-SURGE: new software specifically designed for multistate capture-recapture models
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/dao060141openalex-snapshot
Rapid quantitative detection of chytridiomycosis (Batrachochytrium dendrobatidis) in amphibian samples using real-time Taqman PCR assay
inferredcites →https://doi.org/10.5167/uzh-36147openalex-snapshot
Body size development of captive and free-ranging African spurred tortoises (Geochelone sulcata): High plasticity in reptilian growth rates
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.

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A new species of frog in the Litoria ewingii species group (Anura: Pelodryadidae) from south-eastern Australia
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Improving breed‐and‐release programmes in the face of a threatening pathogen, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1002/ecs2.2499openalex-snapshot
Disease and climate effects on individuals drive post‐reintroduction population dynamics of an endangered amphibian
inferred← citeshttps://doi.org/10.1002/ecs2.4294openalex-snapshot
To treat or not to treat? Experimental pathogen exposure, treatment, and release of a threatened amphibian
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Chytridiomycosis
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Disease-associated change in an amphibian life-history trait
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A Model to Inform Management Actions as a Response to Chytridiomycosis-Associated Decline
inferred← citeshttps://doi.org/10.1016/j.biocon.2016.12.010openalex-snapshot
After the epidemic: Ongoing declines, stabilizations and recoveries in amphibians afflicted by chytridiomycosis
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.05.025openalex-snapshot
A recovery engine strategy for amphibian conservation in the context of disease
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.05.029openalex-snapshot
Conserving Panamanian harlequin frogs by integrating captive-breeding and research programs
inferred← citeshttps://doi.org/10.1016/j.funeco.2015.09.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gecco.2020.e01314openalex-snapshot
Towards a food web based control strategy to mitigate an amphibian panzootic in agricultural landscapes
inferred← citeshttps://doi.org/10.1038/s41586-024-07582-yopenalex-snapshot
Hotspot shelters stimulate frog resistance to chytridiomycosis
inferred← citeshttps://doi.org/10.1038/sdata.2018.33openalex-snapshot
Survival, gene and metabolite responses of Litoria verreauxii alpina frogs to fungal disease chytridiomycosis
inferred← citeshttps://doi.org/10.1071/9781486307425.bk07705_ch29openalex-snapshot
The contribution of captive breeding in zoos to the conservation of Australia’s threatened fauna
inferred← citeshttps://doi.org/10.1071/9781486308392.bk07783_ch06openalex-snapshot
Frog declines and associated management response in south-eastern mainland Australia and Tasmania
inferred← citeshttps://doi.org/10.1071/wr15071openalex-snapshot
Priorities for management of chytridiomycosis in Australia: saving frogs from extinction
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/10.1098/rsob.150251openalex-snapshot
Amphibians with infectious disease increase their reproductive effort: evidence for the terminal investment hypothesis
inferred← citeshttps://doi.org/10.1098/rspb.2022.0586openalex-snapshot
Body condition, skin bacterial communities and disease status: insights from the first release trial of the limosa harlequin frog,Atelopus limosus
inferred← citeshttps://doi.org/10.1098/rstb.2015.0465openalex-snapshot
Overview of chytrid emergence and impacts on amphibians
inferred← citeshttps://doi.org/10.1098/rstb.2016.0207openalex-snapshot
Mitigating amphibian chytridiomycoses in nature
inferred← citeshttps://doi.org/10.1111/1365-2435.13419openalex-snapshot
Effects of hydroperiod on growth, development, survival and immune defences in a temperate amphibian
inferred← citeshttps://doi.org/10.1111/acv.12380openalex-snapshot
Non‐declining amphibians can be important reservoir hosts for amphibian chytrid fungus
inferred← citeshttps://doi.org/10.1111/acv.12459openalex-snapshot
Genetic potential for disease resistance in critically endangered amphibians decimated by chytridiomycosis
inferred← citeshttps://doi.org/10.1111/acv.12940openalex-snapshot
Evaluation of trial reintroductions of two extinct in the wild reptile species on Christmas Island
inferred← citeshttps://doi.org/10.1111/acv.70042openalex-snapshot
Sick Hops: How Infection Boosts Jumping Ability in a Threatened Frog Species
inferred← citeshttps://doi.org/10.1111/aec.13171openalex-snapshot
The hitchhiker's guide to Australian conservation: A parasitological perspective on fauna translocations
inferred← citeshttps://doi.org/10.1111/brv.13025openalex-snapshot
The fitness consequences of wildlife conservation translocations: a meta‐analysis
inferred← citeshttps://doi.org/10.1111/csp2.524openalex-snapshot
Conservation translocations for amphibian species threatened by chytrid fungus: A review, conceptual framework, and recommendations
inferred← citeshttps://doi.org/10.1111/ele.13621openalex-snapshot
Mechanisms underlying host persistence following amphibian disease emergence determine appropriate management strategies
inferred← citeshttps://doi.org/10.1111/evo.14327openalex-snapshot
Declining amphibians might be evolving increased reproductive effort in the face of devastating disease
inferred← citeshttps://doi.org/10.1111/mec.15122openalex-snapshot
Fungal disease and temperature alter skin microbiome structure in an experimental salamander system
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/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/10.1146/annurev-animal-021122-100823openalex-snapshot
Advances in Managing Chytridiomycosis for Australian Frogs: Gradarius Firmus Victoria
inferred← citeshttps://doi.org/10.1186/s12898-018-0189-5openalex-snapshot
Fungal infection has sublethal effects in a lowland subtropical amphibian population
inferred← citeshttps://doi.org/10.1371/journal.pone.0143629openalex-snapshot
Dynamics of Chytridiomycosis during the Breeding Season in an Australian Alpine Amphibian
inferred← citeshttps://doi.org/10.1371/journal.pone.0177860openalex-snapshot
Introduced bullfrogs are associated with increased Batrachochytrium dendrobatidis prevalence and reduced occurrence of Korean treefrogs
inferred← citeshttps://doi.org/10.1371/journal.pone.0241119openalex-snapshot
Chytridiomycosis-induced mortality in a threatened anuran
inferred← citeshttps://doi.org/10.1556/1777.2025.00077openalex-snapshot
Potential causes of geographic variation in the severity of chytridiomycosis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-9696818/v1openalex-snapshot
Fine-Scale Population Structure and Contrasting Connectivity in Remnant Populations of the Alpine Tree Frog
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/10.3389/fimmu.2018.02536openalex-snapshot
Review of the Amphibian Immune Response to Chytridiomycosis, and Future Directions
inferred← citeshttps://doi.org/10.3389/fmicb.2019.01912openalex-snapshot
Effects of Captivity and Season on the Gut Microbiota of the Brown Frog (Rana dybowskii)
inferred← citeshttps://doi.org/10.3390/ani13213379openalex-snapshot
Assessing Disease Risks in Wildlife Translocation Projects: A Comprehensive Review of Disease Incidents
inferred← citeshttps://doi.org/10.7287/peerj.15179v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15179v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15179v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.2925v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Epidermal cell death in frogs with chytridiomycosis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2925v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Epidermal cell death in frogs with chytridiomycosis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2925v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Epidermal cell death in frogs with chytridiomycosis (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.2925v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Epidermal cell death in frogs with chytridiomycosis (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.12712openalex-snapshot
Effectiveness of antifungal treatments during chytridiomycosis epizootics in populations of an endangered frog
inferred← citeshttps://doi.org/10.7717/peerj.15179openalex-snapshot
Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina
inferred← citeshttps://doi.org/10.7717/peerj.2925openalex-snapshot
Epidermal cell death in frogs with chytridiomycosis
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