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Sex Ratios in a Warming World: Thermal Effects on Sex-Biased Survival, Sex Determination, and Sex Reversal

https://doi.org/10.1093/jhered/esab006
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What this work says

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

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Under what conditions do climate‐driven sex ratios enhance versus diminish population persistence?
inferredcites →https://doi.org/10.1002/ece3.2209openalex-snapshot
Dmrt1 polymorphism covaries with sex‐determination patterns in Rana temporaria
inferredcites →https://doi.org/10.1002/ece3.5229openalex-snapshot
Some like it dry: Water restriction overrides heterogametic sex determination in two reptiles
inferredcites →https://doi.org/10.1006/tpbi.2000.1482openalex-snapshot
Carl Düsing (1884) on The Regulation of the Sex-Ratio
inferredcites →https://doi.org/10.1007/s00438-009-0437-7openalex-snapshot
Isolation and development of a molecular sex marker for Bassiana duperreyi, a lizard with XX/XY sex chromosomes and temperature-induced sex reversal
inferredcites →https://doi.org/10.1007/s00442-018-4190-7openalex-snapshot
Does sexual dimorphism predispose dioecious riparian trees to sex ratio imbalances under climate change?
inferredcites →https://doi.org/10.1016/0041-0101(85)90399-xopenalex-snapshot
The structure, development and evolution of reptiles
inferredcites →https://doi.org/10.1016/j.cub.2017.11.057openalex-snapshot
Environmental Warming and Feminization of One of the Largest Sea Turtle Populations in the World
inferredcites →https://doi.org/10.1016/j.cub.2018.09.043openalex-snapshot
Sex reversal
inferredcites →https://doi.org/10.1016/j.cub.2019.06.038openalex-snapshot
The Embryos of Turtles Can Influence Their Own Sexual Destinies
inferredcites →https://doi.org/10.1016/j.ecolmodel.2016.02.011openalex-snapshot
Dispersal and climate warming determine range shift in model reptile populations
inferredcites →https://doi.org/10.1016/j.envexpbot.2014.08.007openalex-snapshot
Sex ratios in dioecious plants in the framework of global change
inferredcites →https://doi.org/10.1016/j.fertnstert.2003.09.051openalex-snapshot
Environmental versus genetic sex determination: a possible factor in dinosaur extinction?
inferredcites →https://doi.org/10.1016/j.jtherbio.2011.10.010openalex-snapshot
Microclimate of American crocodile nests in Banco Chinchorro biosphere reserve, Mexico: Effect on incubation length, embryos survival and hatchlings sex
inferredcites →https://doi.org/10.1016/j.jtherbio.2012.12.001openalex-snapshot
Trade-off between thermal sensitivity, hypoxia tolerance and growth in fish
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.lfs.2018.10.058openalex-snapshot
Testosterone mediates hyperthermic response of mice to heat exposure
inferredcites →https://doi.org/10.1016/j.neubiorev.2010.07.002openalex-snapshot
Sex bias in neuroscience and biomedical research
inferredcites →https://doi.org/10.1016/j.redox.2020.101488openalex-snapshot
Sex differences in the response to oxidative and proteolytic stress
inferredcites →https://doi.org/10.1016/j.tree.2011.03.005openalex-snapshot
Declining body size: a third universal response to warming?
inferredcites →https://doi.org/10.1016/j.ygcen.2013.05.024openalex-snapshot
Environmental stress-induced testis differentiation: Androgen as a by-product of cortisol inactivation
inferredcites →https://doi.org/10.1016/j.ygcen.2014.09.014openalex-snapshot
Effects of the environmental estrogenic contaminants bisphenol A and 17α-ethinyl estradiol on sexual development and adult behaviors in aquatic wildlife species
inferredcites →https://doi.org/10.1016/s0065-2504(08)60212-3openalex-snapshot
Temperature and Organism Size—A Biological Law for Ectotherms?
inferredcites →https://doi.org/10.1016/s1095-6433(03)00178-8openalex-snapshot
An aromatase inhibitor or high water temperature induce oocyte apoptosis and depletion of P450 aromatase activity in the gonads of genetic female zebrafish during sex-reversal
inferredcites →https://doi.org/10.1017/s1367943002001026openalex-snapshot
Manipulating sex ratios for conservation: short-term risks and long-term benefits
inferredcites →https://doi.org/10.1038/266828a0openalex-snapshot
When is sex environmentally determined?
inferredcites →https://doi.org/10.1038/332790a0openalex-snapshot
Environmental sex determination in reptiles
inferredcites →https://doi.org/10.1038/hdy.1981.2openalex-snapshot
Sex ratio evolution when fitness varies
inferredcites →https://doi.org/10.1038/nature15380openalex-snapshot
The genetic sex-determination system predicts adult sex ratios in tetrapods
inferredcites →https://doi.org/10.1038/nclimate1539openalex-snapshot
Thermal tolerance and the global redistribution of animals
inferredcites →https://doi.org/10.1038/ng.2890openalex-snapshot
Whole-genome sequence of a flatfish provides insights into ZW sex chromosome evolution and adaptation to a benthic lifestyle
inferredcites →https://doi.org/10.1038/nplants.2016.109openalex-snapshot
Climate change perils for dioecious plant species
inferredcites →https://doi.org/10.1038/s41437-018-0126-6openalex-snapshot
New locus reveals the genetic architecture of sex reversal in the Chinese tongue sole (Cynoglossus semilaevis)
inferredcites →https://doi.org/10.1038/s41467-018-03833-5openalex-snapshot
Demographic causes of adult sex ratio variation and their consequences for parental cooperation
inferredcites →https://doi.org/10.1038/s41598-017-12405-4openalex-snapshot
Temperature-dependent sex-reversal by a transformer-2 gene-edited mutation in the spotted wing drosophila, Drosophila suzukii
inferredcites →https://doi.org/10.1038/s41598-018-35821-6openalex-snapshot
Optimism for mitigation of climate warming impacts for sea turtles through nest shading and relocation
inferredcites →https://doi.org/10.1038/s41598-019-40597-4openalex-snapshot
Extreme thermal fluctuations from climate change unexpectedly accelerate demographic collapse of vertebrates with temperature-dependent sex determination
inferredcites →https://doi.org/10.1038/s41598-019-42944-xopenalex-snapshot
Warmer waters masculinize wild populations of a fish with temperature-dependent sex determination
inferredcites →https://doi.org/10.1038/sdata.2014.15openalex-snapshot
Tree of Sex: A database of sexual systems
inferredcites →https://doi.org/10.1038/sdata.2018.22openalex-snapshot
GlobTherm, a global database on thermal tolerances for aquatic and terrestrial organisms
inferredcites →https://doi.org/10.1073/pnas.0505172102openalex-snapshot
Sex ratio bias, male aggression, and population collapse in lizards
inferredcites →https://doi.org/10.1073/pnas.1423041112openalex-snapshot
Synthesis of phylogeny and taxonomy into a comprehensive tree of life
inferredcites →https://doi.org/10.1073/pnas.1903586116openalex-snapshot
Research community needs to better appreciate the value of sex-based research
inferredcites →https://doi.org/10.1080/11956860.2003.11682773openalex-snapshot
Assessment of patterns of temperature-dependent sex determination using maximum likelihood model selection
inferredcites →https://doi.org/10.1086/368292openalex-snapshot
Pattern Does Not Equal Process: Exactly When Is Sex Environmentally Determined?
inferredcites →https://doi.org/10.1086/663770openalex-snapshot
Sex and Proximity to Reproductive Maturity Influence the Survival, Final Maturation, and Blood Physiology of Pacific Salmon When Exposed to High Temperature during a Simulated Migration
inferredcites →https://doi.org/10.1093/jhered/esv053openalex-snapshot
Temperature-Dependent Sex Determination under Rapid Anthropogenic Environmental Change: Evolution at a Turtle’s Pace?
inferredcites →https://doi.org/10.1093/treephys/tpx066openalex-snapshot
Sex determines xylem anatomy in a dioecious conifer: hydraulic consequences in a drier world
inferredcites →https://doi.org/10.1096/fj.15-279554openalex-snapshot
Studying both sexes: a guiding principle for biomedicine
inferredcites →https://doi.org/10.1098/rsbl.2009.0702openalex-snapshot
Climate change increases the likelihood of catastrophic avian mortality events during extreme heat waves
inferredcites →https://doi.org/10.1098/rsbl.2019.0867openalex-snapshot
The sex with the reduced sex chromosome dies earlier: a comparison across the tree of life
inferredcites →https://doi.org/10.1098/rspb.2007.1385openalex-snapshot
Climate change and the effects of temperature extremes on Australian flying-foxes
inferredcites →https://doi.org/10.1098/rspb.2009.1807openalex-snapshot
Repeated stress exposure results in a survival–reproduction trade-off inDrosophila melanogaster
inferredcites →https://doi.org/10.1098/rspb.2014.0342openalex-snapshot
Sex-biased survival predicts adult sex ratio variation in wild birds
inferredcites →https://doi.org/10.1098/rspb.2014.0831openalex-snapshot
A novel hypothesis for the adaptive maintenance of environmental sex determination in a turtle
inferredcites →https://doi.org/10.1098/rspb.2015.1970openalex-snapshot
Sex ratio variation shapes the ecological effects of a globally introduced freshwater fish
inferredcites →https://doi.org/10.1098/rspb.2016.0217openalex-snapshot
The behavioural consequences of sex reversal in dragons
inferredcites →https://doi.org/10.1098/rstb.2016.0325openalex-snapshot
Climate-driven shifts in adult sex ratios via sex reversals: the type of sex determination matters
inferredcites →https://doi.org/10.1111/1365-2656.13037openalex-snapshot
The sex‐determination pattern in crocodilians: A systematic review of three decades of research
inferredcites →https://doi.org/10.1111/2041-210x.12593openalex-snapshot
rotl: an R package to interact with the Open Tree of Life data
inferredcites →https://doi.org/10.1111/2041-210x.12628openalex-snapshot
ggtree : an r package for visualization and annotation of phylogenetic trees with their covariates and other associated data
inferredcites →https://doi.org/10.1111/brv.12156openalex-snapshot
What was the ancestral sex‐determining mechanism in amniote vertebrates?
inferredcites →https://doi.org/10.1111/brv.12317openalex-snapshot
Climate change and nesting behaviour in vertebrates: a review of the ecological threats and potential for adaptive responses
inferredcites →https://doi.org/10.1111/brv.12582openalex-snapshot
Cellular calcium and redox regulation: the mediator of vertebrate environmental sex determination?
inferredcites →https://doi.org/10.1111/ecog.00967openalex-snapshot
Climate‐related range shifts – a global multidimensional synthesis and new research directions
inferredcites →https://doi.org/10.1111/ele.12049openalex-snapshot
Sex and stochasticity affect range expansion of experimental invasions
inferredcites →https://doi.org/10.1111/evo.12856openalex-snapshot
Sex-specific survival to maturity and the evolution of environmental sex determination
inferredcites →https://doi.org/10.1111/faf.12096openalex-snapshot
Sperm traits of masculinized fish relative to wild‐type males: a systematic review and meta‐analyses
inferredcites →https://doi.org/10.1111/gcb.12912openalex-snapshot
Transgenerational plasticity mitigates the impact of global warming to offspring sex ratios
inferredcites →https://doi.org/10.1111/gcb.15186openalex-snapshot
Mating patterns influence vulnerability to the extinction vortex
inferredcites →https://doi.org/10.1111/j.0022-1112.2004.00292.xopenalex-snapshot
Thermal tolerance and metabolic physiology among redband trout populations in south‐eastern Oregon
inferredcites →https://doi.org/10.1111/j.1469-1795.2007.00099.xopenalex-snapshot
Manipulating sex ratio to increase population growth: the example of the Lesser Kestrel
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00837.xopenalex-snapshot
SEX REVERSAL: A FOUNTAIN OF YOUTH FOR SEX CHROMOSOMES?
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01098.xopenalex-snapshot
TEMPERATURE-DEPENDENT TURNOVERS IN SEX-DETERMINATION MECHANISMS: A QUANTITATIVE MODEL
inferredcites →https://doi.org/10.1111/jeb.13587openalex-snapshot
Climate change, sex reversal and lability of sex‐determining systems
inferredcites →https://doi.org/10.1111/jfb.14429openalex-snapshot
Effects of global warming on sex ratios in fishes
inferredcites →https://doi.org/10.1111/mec.15596openalex-snapshot
Novel genetic sex markers reveal high frequency of sex reversal in wild populations of the agile frog (Rana dalmatina) associated with anthropogenic land use
inferredcites →https://doi.org/10.1111/oik.05886openalex-snapshot
The weakest link: sensitivity to climate extremes across life stages of marine invertebrates
inferredcites →https://doi.org/10.1126/science.aap8328openalex-snapshot
The histone demethylase KDM6B regulates temperature-dependent sex determination in a turtle species
inferredcites →https://doi.org/10.1126/science.aaz4165openalex-snapshot
Temperature-dependent sex determination is mediated by pSTAT3 repression of Kdm6b
inferredcites →https://doi.org/10.1139/cjfr-2018-0270openalex-snapshot
Sexual differences in growth and defence of Populus yunnanensis under drought stress
inferredcites →https://doi.org/10.1159/000289578openalex-snapshot
A Review of Sex Determining Mechanisms in Geckos (Gekkota: Squamata)
inferredcites →https://doi.org/10.1159/000448797openalex-snapshot
Sex Reversal in Amphibians
inferredcites →https://doi.org/10.1159/000450972openalex-snapshot
Sex Reversal in Reptiles: Reproductive Oddity or Powerful Driver of Evolutionary Change?
inferredcites →https://doi.org/10.1159/000452362openalex-snapshot
The Reversible Sex of Gonochoristic Fish: Insights and Consequences
inferredcites →https://doi.org/10.1186/1472-6785-14-19openalex-snapshot
How do climate-linked sex ratios and dispersal limit range boundaries?
inferredcites →https://doi.org/10.1186/s12862-019-1386-3openalex-snapshot
Sex ratios and bimaturism differ between temperature-dependent and genetic sex-determination systems in reptiles
inferredcites →https://doi.org/10.1186/s12862-021-01747-3openalex-snapshot
Evolutionary and demographic consequences of temperature-induced masculinization under climate warming: the effects of mate choice
inferredcites →https://doi.org/10.1242/dev.152033openalex-snapshot
Dmrt1 induces the male pathway in a turtle with temperature-dependent sex determination
inferredcites →https://doi.org/10.1242/dev.172866openalex-snapshot
The central nervous system acts as a transducer of stress-induced masculinization through corticotropin-releasing hormone B
inferredcites →https://doi.org/10.1242/jeb.037523openalex-snapshot
Oxygen- and capacity-limitation of thermal tolerance: a matrix for integrating climate-related stressor effects in marine ecosystems
inferredcites →https://doi.org/10.1242/jeb.162529openalex-snapshot
Maximum thermal limits of coral reef damselfishes are size-dependent and resilient to near-future ocean acidification
inferredcites →https://doi.org/10.1242/jeb.167858openalex-snapshot
The analysis and interpretation of critical temperatures
inferredcites →https://doi.org/10.1371/journal.pone.0002837openalex-snapshot
Temperature-Dependent Sex Determination in Fish Revisited: Prevalence, a Single Sex Ratio Response Pattern, and Possible Effects of Climate Change
inferredcites →https://doi.org/10.1371/journal.pone.0212504openalex-snapshot
Temperature preference of Nile tilapia (Oreochromis niloticus) juveniles induces spontaneous sex reversal
inferredcites →https://doi.org/10.1371/journal.pone.0221641openalex-snapshot
Changes in DNA methylation during epigenetic-associated sex reversal under low temperature in Takifugu rubripes
inferredcites →https://doi.org/10.1537/ase1887.22.495openalex-snapshot
The descent of man and selection in relation to sex
inferredcites →https://doi.org/10.2307/1446248openalex-snapshot
Sex Determination in Turtles: Diverse Patterns and Some Possible Adaptive Values
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3354/meps11013openalex-snapshot
Early life stages are not always the most sensitive: heat stress responses in the copepod Tigriopus californicus
inferredcites →https://doi.org/10.3354/meps12242openalex-snapshot
Balanced primary sex ratios and resilience to climate change in a major sea turtle population
inferredcites →https://doi.org/10.3390/genes11050588openalex-snapshot
Climate Change and Green Sea Turtle Sex Ratio—Preventing Possible Extinction
inferredcites →https://doi.org/10.5479/si.9781944466213openalex-snapshot
Temperature-Dependent Sex Determination in Vertebrates
inferredcites →https://doi.org/10.5962/bhl.title.2112openalex-snapshot
The descent of man, and selection in relation to sex
inferredcites →https://doi.org/10.5962/bhl.title.27468openalex-snapshot
The genetical theory of natural selection
inferredcites →https://doi.org/10.5962/bhl.title.44516openalex-snapshot
Die Regulierung des Geschlechtsverhaltnisses : bei der Vermehrung der Menschen, Tiere und Pflanzen
inferredcites →https://doi.org/10.7554/elife.56344openalex-snapshot
A 10-year follow-up study of sex inclusion in the biological sciences

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/bies.202200039openalex-snapshot
Asymmetrical sex reversal: Does the type of heterogamety predict propensity for sex reversal?
inferred← citeshttps://doi.org/10.1002/ece3.70219openalex-snapshot
No sex‐dependent mortality in an amphibian upon infection with the chytrid fungus, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1002/ece3.71642openalex-snapshot
Determining Zygosity With Multiplex Kompetitive Allele‐Specific PCR ( mxKASP ) Genotyping
inferred← citeshttps://doi.org/10.1002/ece3.71710openalex-snapshot
Variation in the Adult Sex Ratio and Morphological Traits of Cardisoma guanhumi (Latreille, 1828) in Contrasting Habitats in the Southwest of the Gulf of Mexico
inferred← citeshttps://doi.org/10.1002/ece3.72034openalex-snapshot
Fighting Through the Heat: How Male Aggression Influences Demography Under Recurrent Heatwaves
inferred← citeshttps://doi.org/10.1002/ece3.72720openalex-snapshot
Thermal Tolerance Varies Latitudinally and Broadly Mirrors Genetic Structure in the Seaweed Phyllospora comosa Across Its Entire Latitudinal Range
inferred← citeshttps://doi.org/10.1002/ece3.8822openalex-snapshot
Food deprivation exposes sex‐specific trade‐offs between stress tolerance and life span in the copepod Tigriopus californicus
inferred← citeshttps://doi.org/10.1002/jez.2772openalex-snapshot
Does stress make males? An experiment on the role of glucocorticoids in anuran sex reversal
inferred← citeshttps://doi.org/10.1007/978-981-99-0624-6_4openalex-snapshot
The Application of Molecular Markers in Fish Breeding and Aquaculture
inferred← citeshttps://doi.org/10.1007/s00227-025-04714-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00227-026-04959-7openalex-snapshot
Competition among males for breeding females as a measure of male abundance in sea turtles
inferred← citeshttps://doi.org/10.1007/s10531-025-03157-zopenalex-snapshot
Sex-specific responses to climate change in unisexual bryophytes
inferred← citeshttps://doi.org/10.1007/s11692-024-09626-7openalex-snapshot
Tadpoles Develop Elevated Heat Tolerance in Urban Heat Islands Regardless of Sex
inferred← citeshttps://doi.org/10.1007/s12237-024-01466-0openalex-snapshot
Salt Marsh Habitats and Diamondback Terrapins in a Rapidly Changing Climate: A Review
inferred← citeshttps://doi.org/10.1016/b978-0-443-29068-8.00023-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biocon.2024.110606openalex-snapshot
Climate- and scale-dependent sex ratio in threatened Araucaria forests
inferred← citeshttps://doi.org/10.1016/j.cbd.2024.101219openalex-snapshot
How does temperature rise affect a freshwater catfish Rhamdia quelen? A proteomic approach
inferred← citeshttps://doi.org/10.1016/j.coisb.2026.100577openalex-snapshot
Understanding the temperature response of biological systems: Part I–Phenomenological descriptions and microscopic models
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113638openalex-snapshot
High-temperature stress will put the thermo-sensitive teleost yellow catfish (Tachysurus fulvidraco) in danger through reducing reproductivity
inferred← citeshttps://doi.org/10.1016/j.ejar.2026.09.007openalex-snapshot
Sex distribution and gonadal differentiation in naturally deceased olive ridley turtle (Lepidochelys olivacea) hatchlings from a novel sand-free controlled incubation system
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2021.103102openalex-snapshot
Phenotypic stress response does not influence the upper thermal tolerance of male Atlantic salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2021.103151openalex-snapshot
Sex-specific thermal tolerance limits in the ditch shrimp Palaemon varians: Eco-evolutionary implications under a warming ocean
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2025.104356openalex-snapshot
Sex and reproductive condition shape thermal acclimation strategy in a plethodontid salamander
inferred← citeshttps://doi.org/10.1016/j.marenvres.2025.107749openalex-snapshot
Living on the edge: Temperature and salinity performance curves across levels of biological organization in a shallow water shrimp
inferred← citeshttps://doi.org/10.1016/j.marenvres.2025.107791openalex-snapshot
Costs of thermal adaptation: warm-adapted copepods show increased energetic demands under cold exposure
inferred← citeshttps://doi.org/10.1016/j.marenvres.2026.107927openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mce.2025.112636openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/s0007485325100497openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/s0030605325000389openalex-snapshot
Current distribution of Phelsuma inexpectata, a threatened Réunion Island endemic gecko
inferred← citeshttps://doi.org/10.1038/s41597-023-02268-yopenalex-snapshot
HerpSexDet: the herpetological database of sex determination and sex reversal
inferred← citeshttps://doi.org/10.1038/s42003-022-04223-wopenalex-snapshot
Adult sex ratios: causes of variation and implications for animal and human societies
inferred← citeshttps://doi.org/10.1093/beheco/arae044openalex-snapshot
Effects of inbreeding and elevated rearing temperatures on strategic sperm investment
inferred← citeshttps://doi.org/10.1093/evlett/qrad011openalex-snapshot
Divergent evolution of genetic sex determination mechanisms along environmental gradients
inferred← citeshttps://doi.org/10.1093/jeb/voae123openalex-snapshot
Mitonuclear effects on sex ratio persist across generations in interpopulation hybrids
inferred← citeshttps://doi.org/10.1093/jeb/voaf012openalex-snapshot
Behavioural vs. physiological adaptation: which contributes more to the evolution of complex traits in a warming climate?
inferred← citeshttps://doi.org/10.1093/jme/tjad142openalex-snapshot
Egg hatching success is influenced by the time of thermal stress in four hard tick species
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.001.0001openalex-snapshot
Conservation of Wildlife Populations
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0004openalex-snapshot
Dedication
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0007openalex-snapshot
List of Figures
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0008openalex-snapshot
List of Boxes
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0009openalex-snapshot
List of Symbols
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0010openalex-snapshot
Preface to Third Edition
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0011openalex-snapshot
Preface to Second Edition
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0012openalex-snapshot
Preface to First Edition
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0013openalex-snapshot
Epilogue
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.002.0014openalex-snapshot
Credits for Epigraphs
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0001openalex-snapshot
The big picture
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0002openalex-snapshot
Gaining reliable knowledge
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0003openalex-snapshot
Genetic concepts and tools to support wildlife population ecology
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0004openalex-snapshot
Estimating population size and vital rates
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0005openalex-snapshot
Exponential (or geometric) change
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0006openalex-snapshot
All stage classes are not equal in their effects on population growth
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0007openalex-snapshot
Density-dependent population change
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0008openalex-snapshot
Predation and wildlife populations
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0009openalex-snapshot
Genetic variation and fitness of wildlife populations
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0010openalex-snapshot
Dynamics of multiple populations
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0011openalex-snapshot
Population responses to human-caused stressors: Move, adjust, or die
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0012openalex-snapshot
Dynamics of small and declining populations
inferred← citeshttps://doi.org/10.1093/oso/9780192898166.003.0013openalex-snapshot
Sustainable harvest principles, models, and best practices
inferred← citeshttps://doi.org/10.1093/treephys/tpad081openalex-snapshot
Artificial warming affects sugar signals and flavonoid accumulation to improve female willows’ growth faster than males
inferred← citeshttps://doi.org/10.1101/2022.12.13.518051openalex-snapshot
Egg hatching success is significantly influenced by the time of thermal stress in multiple hard tick species
inferred← citeshttps://doi.org/10.1101/2023.08.25.554788openalex-snapshot
Infection with the chytrid fungus ( Batrachochytrium dendrobatidis ) may distort sex ratio via sex reversal but not sex-dependent mortality in a common Eurasian amphibian
inferred← citeshttps://doi.org/10.1101/2024.02.01.578518openalex-snapshot
Effects of inbreeding and elevated rearing temperatures on strategic sperm production
inferred← citeshttps://doi.org/10.1101/2024.10.25.620256openalex-snapshot
Determining zygosity with multiplex Kompetitive Allele-Specific PCR (mxKASP) genotyping
inferred← citeshttps://doi.org/10.1101/2025.03.31.646346openalex-snapshot
Fighting Through the Heat: How Sexual Selection Influences Demography Under Recurrent Heatwaves
inferred← citeshttps://doi.org/10.1111/are.15911openalex-snapshot
Effect of temperature on sex and steroid hormones of purple mud crab, Scylla tranquebarica (Fabricius, 1798) during egg incubation, larvae rearing and juvenile production
inferred← citeshttps://doi.org/10.1111/eva.70093openalex-snapshot
Higher Sex‐Reversal Rate of Urban Frogs in a Common‐Garden Experiment Suggests Adaptive Microevolution
inferred← citeshttps://doi.org/10.1111/gcb.17014openalex-snapshot
Disentangling the drivers of decadal body size decline in an insect population
inferred← citeshttps://doi.org/10.1111/gcb.17553openalex-snapshot
When the Going Gets Tough, the Females Get Going: Sex‐Specific Physiological Responses to Simultaneous Exposure to Hypoxia and Marine Heatwave Events in a Ubiquitous Copepod
inferred← citeshttps://doi.org/10.1111/gcb.70558openalex-snapshot
Cryptic Reproductive Costs of Heatwaves for Animal Populations
inferred← citeshttps://doi.org/10.1111/gcb.70807openalex-snapshot
Transgenerational Heat Exposure Triggers Unexpected Compensatory Sex Ratio Responses in a Temperature‐Sensitive Fish Under Climate Warming
inferred← citeshttps://doi.org/10.1111/gcb.70950openalex-snapshot
These Boots Are Made for Walking: Sex‐Specific Physiological and Metabolomic Strategies Reflect Male‐Skewed Vulnerability to Ocean Warming in a Keystone Amphipod
inferred← citeshttps://doi.org/10.1111/jbi.70116openalex-snapshot
Human‐Induced Extinction Risk of the World's Crocodilians and Chelonians
inferred← citeshttps://doi.org/10.1111/jfb.70361openalex-snapshot
Assessment of two minimally invasive methodologies for sex identification in the European eel, Anguilla anguilla
inferred← citeshttps://doi.org/10.1128/spectrum.02271-24openalex-snapshot
Frenemy: adaptive temperate phage_SAP_1432 supports Staphylococcus aureus survival in changing temperatures
inferred← citeshttps://doi.org/10.1152/ajpregu.00120.2025openalex-snapshot
Sex differences in stress response in the marine copepod, Calanus finmarchicus
inferred← citeshttps://doi.org/10.1186/s12862-023-02172-4openalex-snapshot
Heat-induced female biased sex ratio during development is not mitigated after prolonged thermal selection
inferred← citeshttps://doi.org/10.14202/vetworld.2026.2105-2116openalex-snapshot
Effects of controlled artificial incubation on hatching success, morphometric traits, and early physiological indicators in olive ridley sea turtles (Lepidochelys olivacea) from Banyuwangi coast, Indonesia
inferred← citeshttps://doi.org/10.2139/ssrn.5564718openalex-snapshot
Sex and reproductive condition shape thermal acclimation strategy in a plethodontid salamander
inferred← citeshttps://doi.org/10.3354/esr01215openalex-snapshot
High female desert tortoise mortality in the western Sonoran Desert during California’s epic 2012-2016 drought
inferred← citeshttps://doi.org/10.3389/fevo.2021.808621openalex-snapshot
Turtle Nest-Site Choice, Anthropogenic Challenges, and Evolutionary Potential for Adaptation
inferred← citeshttps://doi.org/10.3389/fevo.2022.884159openalex-snapshot
Natural and Engineered Sex Ratio Distortion in Insects
inferred← citeshttps://doi.org/10.3390/ani12202731openalex-snapshot
Climate Change and Dispersal Ability Jointly Affects the Future Distribution of Crocodile Lizards
inferred← citeshttps://doi.org/10.3390/ani12202887openalex-snapshot
Testicular Transcriptome of Males and Pseudo-Males Provides Important New Insight into Sex Reversal of Rana dybowskii
inferred← citeshttps://doi.org/10.3390/ani16010004openalex-snapshot
Thermal Limits of the Estuarine Amphipod Melita palmata Under Different Salinities and Its Relevance for Aquaculture Production
inferred← citeshttps://doi.org/10.3390/horticulturae12070874openalex-snapshot
Integrating Genomic Markers and Non-Invasive Phenotyping for Early Sex Identification in Horticultural Plants: A Mechanism-Guided Framework
inferred← citeshttps://doi.org/10.3390/ijms242116002openalex-snapshot
Exploring the Effects of Rearing Densities on Epigenetic Modifications in the Zebrafish Gonads
inferred← citeshttps://doi.org/10.3390/insects16010080openalex-snapshot
The Thermal Tolerance of Springtails in a Tropical Cave, with the Description of a New Coecobrya Species (Collembola: Entomobryidae) from Thailand
inferred← citeshttps://doi.org/10.36953/ecj.37403257openalex-snapshot
Sex ratio of Nemacheilus multifasciatus (Hillstream Loach) in the Heval River of Garhwal Himalaya, Uttarakhand, India
inferred← citeshttps://doi.org/10.6084/m9.figshare.24494224openalex-snapshot
Additional file 1 of Heat-induced female biased sex ratio during development is not mitigated after prolonged thermal selection
inferred← citeshttps://doi.org/10.6084/m9.figshare.24494503openalex-snapshot
Additional file 2 of Heat-induced female biased sex ratio during development is not mitigated after prolonged thermal selection
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635122openalex-snapshot
Additional file 3 of Heat-induced female biased sex ratio during development is not mitigated after prolonged thermal selection
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635125openalex-snapshot
Additional file 4 of Heat-induced female biased sex ratio during development is not mitigated after prolonged thermal selection
inferred← citeshttps://doi.org/10.64898/2026.06.25.734438openalex-snapshot
Thermally driven sex reversal reveals divergent sex determination dynamics in wild viviparous reptile populations
inferred← citeshttps://doi.org/10.9734/ijecc/2024/v14i74274openalex-snapshot
Abiotic Factors as Game Changer in Sex Ratio Distortion of Insects
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