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Evolutionarily significant units of the critically endangered leaf frog Pithecopus ayeaye (Anura, Phyllomedusidae) are not effectively preserved by the Brazilian protected areas network

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

inferredcites →https://doi.org/10.1002/ece3.3261openalex-snapshot
Evolutionarily significant units of the critically endangered leaf frog Pithecopus ayeaye (Anura, Phyllomedusidae) are not effectively preserved by the Brazilian protected areas network
inferredcites →https://doi.org/10.1002/joc.1276openalex-snapshot
Very high resolution interpolated climate surfaces for global land areas
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PCR Primers and Amplification Methods for 12S Ribosomal DNA, the Control Region, Cytochrome Oxidase I, and Cytochromebin Bufonids and Other Frogs, and an Overview of PCR Primers which Have Amplified DNA in Amphibians Successfully
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1007/s10531-007-9156-8openalex-snapshot
Plant communities on ironstone outcrops: a diverse and endangered Brazilian ecosystem
inferredcites →https://doi.org/10.1007/s10531-013-0605-2openalex-snapshot
Climate change threatens protected areas of the Atlantic Forest
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From widespread to microendemic: molecular and acoustic analyses show that Ischnocnema guentheri (Amphibia: Brachycephalidae) is endemic to Rio de Janeiro, Brazil
inferredcites →https://doi.org/10.1007/s10682-015-9774-7openalex-snapshot
Genetic divergence in tropical anurans: deeper phylogeographic structure in forest specialists and in topographically complex regions
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Ecology and evolution of plant diversity in the endangered campo rupestre: a neglected conservation priority
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New primers for the amplification and sequencing of nuclear loci in a taxonomically wide set of reptiles and amphibians
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TRACER version 1.1
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Defining ‘Evolutionarily Significant Units’ for conservation
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The amphibian decline crisis: A watershed for conservation biology?
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Extreme population divergence and conservation implications for the rare endangered Atlantic Forest sloth, Bradypus torquatus (Pilosa: Bradypodidae)
inferredcites →https://doi.org/10.1016/j.biocon.2013.02.018openalex-snapshot
Effectiveness of terrestrial protected areas in reducing habitat loss and population declines
inferredcites →https://doi.org/10.1016/j.biocon.2014.08.012openalex-snapshot
Rarity as an indicator of endangerment in neotropical frogs
inferredcites →https://doi.org/10.1016/j.biocon.2015.07.028openalex-snapshot
Amphibian conservation, land-use changes and protected areas: A global overview
inferredcites →https://doi.org/10.1016/j.biocon.2016.12.018openalex-snapshot
Elevation range shift after 40 years: The amphibians of Mount Gede Pangrango National Park revisited
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Estimating optimal complexity for ecological niche models: A jackknife approach for species with small sample sizes
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Challenges for the conservation of vanishing megadiverse rupestrian grasslands
inferredcites →https://doi.org/10.1016/j.ncon.2015.04.001openalex-snapshot
Habitat loss and the effectiveness of protected areas in the Cerrado Biodiversity Hotspot
inferredcites →https://doi.org/10.1016/j.tree.2006.09.010openalex-snapshot
Ensemble forecasting of species distributions
inferredcites →https://doi.org/10.1016/j.tree.2006.10.004openalex-snapshot
Model use in phylogenetics: nine key questions
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Approximate Bayesian Computation (ABC) in practice
inferredcites →https://doi.org/10.1038/35002501openalex-snapshot
Biodiversity hotspots for conservation priorities
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A globally coherent fingerprint of climate change impacts across natural systems
inferredcites →https://doi.org/10.1038/nature02422openalex-snapshot
Effectiveness of the global protected area network in representing species diversity
inferredcites →https://doi.org/10.1038/nature13685openalex-snapshot
Comparative population genomics in animals uncovers the determinants of genetic diversity
inferredcites →https://doi.org/10.1038/nature13947openalex-snapshot
The performance and potential of protected areas
inferredcites →https://doi.org/10.1038/nclimate1191openalex-snapshot
Cryptic biodiversity loss linked to global climate change
inferredcites →https://doi.org/10.1038/nmeth.2109openalex-snapshot
jModelTest 2: more models, new heuristics and parallel computing
inferredcites →https://doi.org/10.1038/nrg2844openalex-snapshot
Genomics and the future of conservation genetics
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Molecular ecology of social behaviour: analyses of breeding systems and genetic structure
inferredcites →https://doi.org/10.1046/j.1365-294x.2001.t01-1-01411.xopenalex-snapshot
Adaptive evolutionary conservation: towards a unified concept for defining conservation units
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01910.xopenalex-snapshot
Huge populations and old species of Costa Rican and Panamanian dirt frogs inferred from mitochondrial and nuclear gene sequences
inferredcites →https://doi.org/10.1080/00222933.2014.896486openalex-snapshot
Reproductive site selection in the leaf-frogPhyllomedusa azureaCope, 1862 (Anura: Hylidae) in altered areas of the Brazilian Cerrado
inferredcites →https://doi.org/10.1080/00222933.2017.1296196openalex-snapshot
Mating behaviour, territoriality and natural history notes ofPhyllomedusa ayeayeLutz, 1966 (Hylidae: Phyllomedusinae) in south-eastern Brazil
inferredcites →https://doi.org/10.1080/10635150500234534openalex-snapshot
Asynchronous Colonization of Madagascar by the Four Endemic Clades of Primates, Tenrecs, Carnivores, and Rodents as Inferred from Nuclear Genes
inferredcites →https://doi.org/10.1080/10635150500234625openalex-snapshot
Hylid Frog Phylogeny and Sampling Strategies for Speciose Clades
inferredcites →https://doi.org/10.1080/10635150600863109openalex-snapshot
Incorporating Allelic Variation for Reconstructing the Evolutionary History of Organisms from Multiple Genes: An Example from Rosa in North America
inferredcites →https://doi.org/10.1080/14772000.2014.972477openalex-snapshot
Biogeographic patterns, origin and speciation of the endemic birds from eastern Brazilian mountaintops: a review
inferredcites →https://doi.org/10.1086/319501openalex-snapshot
A New Statistical Method for Haplotype Reconstruction from Population Data
inferredcites →https://doi.org/10.1093/aob/mcp157openalex-snapshot
Phylogeography and disjunct distribution in Lychnophora ericoides (Asteraceae), an endangered cerrado shrub species
inferredcites →https://doi.org/10.1093/bioinformatics/18.2.337openalex-snapshot
Generating samples under a Wright–Fisher neutral model of genetic variation
inferredcites →https://doi.org/10.1093/bioinformatics/bti803openalex-snapshot
Comparison of Bayesian and maximum-likelihood inference of population genetic parameters
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/bioinformatics/btn419openalex-snapshot
Inference of structure in subdivided populations at low levels of genetic differentiation—the correlated allele frequencies model revisited
inferredcites →https://doi.org/10.1093/bioinformatics/btp187openalex-snapshot
DnaSP v5: a software for comprehensive analysis of DNA polymorphism data
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/genetics/123.3.585openalex-snapshot
Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.
inferredcites →https://doi.org/10.1093/genetics/134.2.659openalex-snapshot
A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. IV. Nested analyses with cladogram uncertainty and recombination.
inferredcites →https://doi.org/10.1093/genetics/163.1.367openalex-snapshot
Bayesian Analysis of Genetic Differentiation Between Populations
inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
inferredcites →https://doi.org/10.1093/molbev/msx126openalex-snapshot
StarBEAST2 Brings Faster Species Tree Inference and Accurate Estimates of Substitution Rates
inferredcites →https://doi.org/10.1093/nar/gkm306openalex-snapshot
Primer3Plus, an enhanced web interface to Primer3
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025875openalex-snapshot
A Comparative Summary of Genetic Distances in the Vertebrates from the Mitochondrial Cytochome b Gene
inferredcites →https://doi.org/10.1093/sysbio/41.3.273openalex-snapshot
Evolutionary Relationships Within the Ensatina Eschscholtzii Complex Confirm the Ring Species Interpretation
inferredcites →https://doi.org/10.1093/sysbio/46.3.523openalex-snapshot
Gene Trees in Species Trees
inferredcites →https://doi.org/10.1111/2041-210x.12343openalex-snapshot
Flexible methods for estimating genetic distances from single nucleotide polymorphisms
inferredcites →https://doi.org/10.1111/2041-210x.12410openalex-snapshot
popart : full‐feature software for haplotype network construction
inferredcites →https://doi.org/10.1111/aec.12215openalex-snapshot
Observed range dynamics of S outh A frican amphibians under conditions of global change
inferredcites →https://doi.org/10.1111/ddi.12098openalex-snapshot
Integrating ensemble species distribution modelling and statistical phylogeography to inform projections of climate change impacts on species distributions
inferredcites →https://doi.org/10.1111/j.0906-7590.2006.04700.xopenalex-snapshot
The effect of sample size and species characteristics on performance of different species distribution modeling methods
inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01594.xopenalex-snapshot
ORIGINAL ARTICLE: Predicting species distributions from small numbers of occurrence records: a test case using cryptic geckos in Madagascar
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02683.xopenalex-snapshot
Molecular evidence for glacial refugia of mountain plants in the European Alps
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.02908.xopenalex-snapshot
Refugia, differentiation and postglacial migration in arctic‐alpine Eurasia, exemplified by the mountain avens ( Dryas octopetala L.)
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03731.xopenalex-snapshot
Nested clade analysis: an extensively validated method for strong phylogeographic inference
inferredcites →https://doi.org/10.1111/j.1466-8238.2007.00355.xopenalex-snapshot
Macroecology and extinction risk correlates of frogs
inferredcites →https://doi.org/10.1111/j.1471-8286.2005.01031.xopenalex-snapshot
G eneland : a computer package for landscape genetics
inferredcites →https://doi.org/10.1111/j.1472-4642.2008.00482.xopenalex-snapshot
Effects of sample size on the performance of species distribution models
inferredcites →https://doi.org/10.1111/j.1474-919x.2012.01268.xopenalex-snapshot
A new species of Cinclodes from the Espinhaço Range, southeastern Brazil: insights into the biogeographical history of the South American highlands
inferredcites →https://doi.org/10.1111/j.1523-1739.2005.00100.xopenalex-snapshot
Gaia's Handmaidens: the Orlog Model for Conservation Biology
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Predicting the Probability of Outbreeding Depression
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AMPHIBIAN DNA SHOWS MARKED GENETIC STRUCTURE AND TRACKS PLEISTOCENE CLIMATE CHANGE IN NORTHEASTERN BRAZIL
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00482.xopenalex-snapshot
ENVIRONMENTAL NICHE EQUIVALENCY VERSUS CONSERVATISM: QUANTITATIVE APPROACHES TO NICHE EVOLUTION
inferredcites →https://doi.org/10.1111/j.1600-0587.2009.06142.xopenalex-snapshot
ENMTools: a toolbox for comparative studies of environmental niche models
inferredcites →https://doi.org/10.1111/j.1600-0587.2009.06196.xopenalex-snapshot
Partitioning and mapping uncertainties in ensembles of forecasts of species turnover under climate change
inferredcites →https://doi.org/10.1111/j.1600-0587.2011.06545.xopenalex-snapshot
The effects of small sample size and sample bias on threshold selection and accuracy assessment of species distribution models
inferredcites →https://doi.org/10.1111/j.1749-6632.2010.05909.xopenalex-snapshot
The complexity of amphibian population declines: understanding the role of cofactors in driving amphibian losses
inferredcites →https://doi.org/10.1111/j.1755-0998.2009.02732.xopenalex-snapshot
seqphase : a web tool for interconverting phase input/output files and fasta sequence alignments
inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00179.xopenalex-snapshot
abc: an R package for approximate Bayesian computation (ABC)
inferredcites →https://doi.org/10.1111/mec.12152openalex-snapshot
The impact of global climate change on genetic diversity within populations and species
inferredcites →https://doi.org/10.1111/mec.12347openalex-snapshot
Model selection as a tool for phylogeographic inference: an example from the willow S alix melanopsis
inferredcites →https://doi.org/10.1111/mec.12413openalex-snapshot
How to fail at species delimitation
inferredcites →https://doi.org/10.1111/mec.12780openalex-snapshot
Interglacial microrefugia and diversification of a cactus species complex: phylogeography and palaeodistributional reconstructions for Pilosocereus aurisetus and allies
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.1206432openalex-snapshot
Rapid Range Shifts of Species Associated with High Levels of Climate Warming
inferredcites →https://doi.org/10.1126/science.1246752openalex-snapshot
The biodiversity of species and their rates of extinction, distribution, and protection
inferredcites →https://doi.org/10.1127/0941-2948/2013/0507openalex-snapshot
Köppen's climate classification map for Brazil
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Divergence with Gene Flow: Models and Data
inferredcites →https://doi.org/10.1146/annurev.ecolsys.39.110707.173529openalex-snapshot
The Ecological Performance of Protected Areas
inferredcites →https://doi.org/10.11646/zootaxa.2044.1.4openalex-snapshot
Remarks on A new Phyllomedusa Wagler (Anura, Hylidae) with reticulated pattern on flanks from Southeastern Brazil
inferredcites →https://doi.org/10.11646/zootaxa.2226.1.5openalex-snapshot
Phyllomedusa itacolomi Caramaschi, Cruz & Feio, 2006, a junior synonym of Phyllomedusa ayeaye (B. Lutz, 1966) (Hylidae, Phyllomedusinae)
inferredcites →https://doi.org/10.1186/1471-2156-6-13openalex-snapshot
Isolation by distance, web service
inferredcites →https://doi.org/10.1186/s12983-016-0163-zopenalex-snapshot
Conservation of genetic uniqueness of populations may increase extinction likelihood of endangered species: the case of Australian mammals
inferredcites →https://doi.org/10.1371/journal.pcbi.1000113openalex-snapshot
Decoding of Superimposed Traces Produced by Direct Sequencing of Heterozygous Indels
inferredcites →https://doi.org/10.1371/journal.pcbi.1003537openalex-snapshot
BEAST 2: A Software Platform for Bayesian Evolutionary Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0125847openalex-snapshot
Hitting an Unintended Target: Phylogeography of Bombus brasiliensis Lepeletier, 1836 and the First New Brazilian Bumblebee Species in a Century (Hymenoptera: Apidae)
inferredcites →https://doi.org/10.1525/bio.2011.61.10.5openalex-snapshot
Climate Change and Species Range Dynamics in Protected Areas
inferredcites →https://doi.org/10.1534/genetics.104.033803openalex-snapshot
A Spatial Statistical Model for Landscape Genetics
inferredcites →https://doi.org/10.1534/genetics.109.112532openalex-snapshot
Unified Framework to Evaluate Panmixia and Migration Direction Among Multiple Sampling Locations
inferredcites →https://doi.org/10.15560/3.2.156openalex-snapshot
Amphibia, Anura, Phyllomedusa ayeaye (B. Lutz, 1966): distribution extension, new state record, and geographic distribution map
inferredcites →https://doi.org/10.1590/s1984-46702015000400001openalex-snapshot
Advertisement and release calls of Phyllomedusa ayeaye (Anura: Hylidae) with comments on the social context of emission
inferredcites →https://doi.org/10.1890/10-1171.1openalex-snapshot
Ecological niche modeling in Maxent: the importance of model complexity and the performance of model selection criteria
inferredcites →https://doi.org/10.2305/iucn.uk.2010-2.rlts.t55839a11378310.enopenalex-snapshot
Phyllomedusa ayeaye: Ulisses Caramaschi, Carlos Alberto Gonçalves da Cruz, Raphael Lima, Reuber Brandão
inferredcites →https://doi.org/10.2307/1441130openalex-snapshot
Pithecopus ayeaye, a New Brazilian Hylid with Vertical Pupils and Grasping Feet
inferredcites →https://doi.org/10.23943/princeton/9780691136868.001.0001openalex-snapshot
Ecological Niches and Geographic Distributions (MPB-49)
inferredcites →https://doi.org/10.2737/rm-gtr-264openalex-snapshot
Biodiversity and management of the Madrean Archipelago: The Sky Islands of southwestern United States and northwestern Mexico
inferredcites →https://doi.org/10.2994/057.004.0203openalex-snapshot
The Tadpole of Phyllomedusa itacolomi (Anura, Hylidae), with a Description of the Internal Oral Morphology
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3390/d2010047openalex-snapshot
Global Amphibian Declines, Loss of Genetic Diversity and Fitness: A Review
inferredcites →https://doi.org/10.7312/nei-92038openalex-snapshot
Molecular Evolutionary Genetics

What points at this work

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

inferred← citeshttps://doi.org/10.35249/rche.49.4.23.18zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/ece3.9802openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12041-019-1159-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91240-2.00013-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jnc.2018.07.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jnc.2024.126731openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.140269openalex-snapshot
Niche divergence of evolutionarily significant units with implications for repopulation programs of the world's largest amphibians
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.11.022openalex-snapshot
Cryptic diversity in Brazilian endemic monkey frogs (Hylidae, Phyllomedusinae, Pithecopus) revealed by multispecies coalescent and integrative approaches
inferred← citeshttps://doi.org/10.1016/j.ympev.2021.107113openalex-snapshot
Quaternary climatic fluctuations influence the demographic history of two species of sky-island endemic amphibians in the Neotropics
inferred← citeshttps://doi.org/10.1073/pnas.2406343121openalex-snapshot
Large-scale genome sequencing of giant pandas improves the understanding of population structure and future conservation initiatives
inferred← citeshttps://doi.org/10.1080/03949370.2024.2444270openalex-snapshot
Evidence of escalated aggressive calling behavior in a male agonistic interaction of the reticulated leaf frog Pithecopus ayeaye
inferred← citeshttps://doi.org/10.1093/biolinnean/blaa142openalex-snapshot
Evidence of introgression in endemic frogs from thecampo rupestrecontradicts the reduced hybridization hypothesis
inferred← citeshttps://doi.org/10.1093/evolut/qpad010openalex-snapshot
Geographic isolation alone does not explain divergence of a group of orchid species across Brazil’scampos rupestressky-islandsIsolamento geográfico por si só não explica a divergência de um grupo de espécies de orquídeas nos campos rupestres do Brasil
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaf108openalex-snapshot
Diversification in old, climatically buffered, infertile landscapes: tracing the evolutionary history of a frog clade (Bokermannohyla: Hylidae) that is endemic to campo rupestre
inferred← citeshttps://doi.org/10.1111/aec.70252openalex-snapshot
Wider Yet Fragmented: Distributional Expansion and Conservation Insights for the Monkey Frog Pithecopus centralis
inferred← citeshttps://doi.org/10.1111/csp2.13106openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/ddi.13299openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/zsc.12470openalex-snapshot
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inferred← citeshttps://doi.org/10.11609/jott.8694.16.4.25040-25048openalex-snapshot
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inferred← citeshttps://doi.org/10.1590/1676-0611-bn-2024-1640openalex-snapshot
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inferred← citeshttps://doi.org/10.1655/0018-0831.294openalex-snapshot
Anuran Distribution in a Highly Diverse Region of the Atlantic Forest: The Mantiqueira Mountain Range in Southeastern Brazil
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2206377/v1openalex-snapshot
Marine introgressions and Andean uplift drives diversification in neotropical Monkey tree frogs (Anura,Phyllomedusinae)
inferred← citeshttps://doi.org/10.3390/d14070542openalex-snapshot
Integrative Phylogeography Reveals Conservation Priorities for the Giant Anteater Myrmecophaga tridactyla in Brazil
inferred← citeshttps://doi.org/10.67174/f8k9hd75openalex-snapshot
Pithecopus ayeaye Lutz, 1966 em sua localidade tipo – Um projeto para entender as principais ameaças e perspectivas futuras para conservação
inferred← citeshttps://doi.org/10.7717/peerj.15393openalex-snapshot
Integrative species delimitation helps to find the hidden diversity of the leaf-litter frog Ischnocnema manezinho (Garcia, 1996) (Anura, Brachycephalidae), endemic to the southern Atlantic Forest
inferred← citeshttps://doi.org/10.7717/peerj.17232openalex-snapshot
Marine introgressions and Andean uplift have driven diversification in neotropical Monkey tree frogs (Anura, Phyllomedusinae)
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