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Sexual conflict mediated by ecological sex differences can generate diverse patterns of transgenerational plasticity
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A paternal environmental legacy: Evidence for epigenetic inheritance through the male germ line
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Epigenetic influence of social experiences across the lifespan
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Parental care improves offspring survival and growth in burying beetles
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Environmental Stress as a Developmental Cue: Corticotropin-Releasing Hormone Is a Proximate Mediator of Adaptive Phenotypic Plasticity in Amphibian Metamorphosis
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Survival in king penguins Aptenodytes patagonicus: temporal and sex-specific effects of environmental variability
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The relationship between ecological segregation and sexual body size dimorphism in large herbivores
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Optimal rates of dispersal. III. Parent-offspring conflict
inferredcites →https://doi.org/10.1016/0169-5347(87)90081-4openalex-snapshot
Sex-biased dispersal and inbreeding avoidance in birds and mammals
inferredcites →https://doi.org/10.1016/0169-5347(91)90210-oopenalex-snapshot
Predation risk as a cost of reproduction
inferredcites →https://doi.org/10.1016/j.biopsych.2010.05.028openalex-snapshot
Early Life Programming and Neurodevelopmental Disorders
inferredcites →https://doi.org/10.1016/j.cell.2012.10.020openalex-snapshot
Daddy Issues: Paternal Effects on Phenotype
inferredcites →https://doi.org/10.1016/j.cell.2014.02.045openalex-snapshot
Transgenerational Epigenetic Inheritance: Myths and Mechanisms
inferredcites →https://doi.org/10.1016/j.neubiorev.2004.12.002openalex-snapshot
Maternal hormones as a tool to adjust offspring phenotype in avian species
inferredcites →https://doi.org/10.1016/j.neubiorev.2014.11.013openalex-snapshot
Stress-induced perinatal and transgenerational epigenetic programming of brain development and mental health
inferredcites →https://doi.org/10.1016/j.tem.2009.12.007openalex-snapshot
Epigenetic transgenerational actions of environmental factors in disease etiology
inferredcites →https://doi.org/10.1016/j.tree.2008.04.005openalex-snapshot
Developmental plasticity and the evolution of parental effects
inferredcites →https://doi.org/10.1016/j.tree.2008.12.005openalex-snapshot
Intralocus sexual conflict
inferredcites →https://doi.org/10.1016/j.tree.2011.02.004openalex-snapshot
Intralocus sexual conflict resolved through gene duplication
inferredcites →https://doi.org/10.1016/j.tree.2014.07.009openalex-snapshot
What is a paternal effect?
inferredcites →https://doi.org/10.1016/j.yhbeh.2010.05.004openalex-snapshot
Sex-specificity in transgenerational epigenetic programming
inferredcites →https://doi.org/10.1016/s0020-7519(96)80001-4openalex-snapshot
Sex Differences in Parasite Infections: Patterns and Processes
inferredcites →https://doi.org/10.1016/s0065-2881(08)00002-3openalex-snapshot
Chapter 2 Sexual Segregation in Marine Fish, Reptiles, Birds and Mammals
inferredcites →https://doi.org/10.1016/s0065-3454(08)00006-5openalex-snapshot
Chapter 6 Information Warfare and Parent–Offspring Conflict
inferredcites →https://doi.org/10.1016/s0169-5347(00)02063-2openalex-snapshot
Maternal effects, paternal effects and sexual selection
inferredcites →https://doi.org/10.1016/s1095-6433(02)00045-4openalex-snapshot
Climate variations and the physiological basis of temperature dependent biogeography: systemic to molecular hierarchy of thermal tolerance in animals
inferredcites →https://doi.org/10.1017/cbo9780511525629openalex-snapshot
Sexual Segregation in Vertebrates
inferredcites →https://doi.org/10.1038/43425openalex-snapshot
Transgenerational induction of defences in animals and plants
inferredcites →https://doi.org/10.1038/hdy.1956.28openalex-snapshot
Further selection experiments on industrial melanism in the Lepidoptera
inferredcites →https://doi.org/10.1038/nature05774openalex-snapshot
Sexual dimorphism and adaptive radiation in Anolis lizards
inferredcites →https://doi.org/10.1038/nature24300openalex-snapshot
Embryonic epigenetic reprogramming by a pioneer transcription factor in plants
inferredcites →https://doi.org/10.1038/nn.4112openalex-snapshot
Sex differences and stress across the lifespan
inferredcites →https://doi.org/10.1038/nn1276openalex-snapshot
Epigenetic programming by maternal behavior
inferredcites →https://doi.org/10.1038/nrendo.2016.87openalex-snapshot
The role of diet and exercise in the transgenerational epigenetic landscape of T2DM
inferredcites →https://doi.org/10.1038/nrg.2016.106openalex-snapshot
Epigenetic inheritance of acquired traits through sperm RNAs and sperm RNA modifications
inferredcites →https://doi.org/10.1038/nrg2167openalex-snapshot
The evolution of sex-biased genes and sex-biased gene expression
inferredcites →https://doi.org/10.1038/nrm4048openalex-snapshot
Epigenetic regulation of ageing: linking environmental inputs to genomic stability
inferredcites →https://doi.org/10.1038/sj.ejhg.5201538openalex-snapshot
Sex-specific, male-line transgenerational responses in humans
inferredcites →https://doi.org/10.1038/srep41926openalex-snapshot
Limb proportions show developmental plasticity in response to embryo movement
inferredcites →https://doi.org/10.1073/pnas.96.2.570openalex-snapshot
Experimental demonstration that offspring sex ratio varies with maternal condition
inferredcites →https://doi.org/10.1073/pnas.96.9.5083openalex-snapshot
Experimental removal of sexual selection reverses intersexual antagonistic coevolution and removes a reproductive load
inferredcites →https://doi.org/10.1073/pnas.98.4.1671openalex-snapshot
Negative genetic correlation for adult fitness between sexes reveals ontogenetic conflict in Drosophila
inferredcites →https://doi.org/10.1086/285207openalex-snapshot
Intersexual Dietary Divergence and the Evolution of Sexual Dimorphism in Snakes
inferredcites →https://doi.org/10.1086/416458openalex-snapshot
Ecological Causes for the Evolution of Sexual Dimorphism: A Review of the Evidence
inferredcites →https://doi.org/10.1086/498946openalex-snapshot
Nonrandom Mating Preserves Intrasexual Polymorphism and Stops Population Differentiation in Sexual Conflict
inferredcites →https://doi.org/10.1086/702341openalex-snapshot
Ecological Consequences Of Sexually Selected Traits: An Eco-Evolutionary Perspective
inferredcites →https://doi.org/10.1093/eep/dvw003openalex-snapshot
Transgenerational plasticity is sex-dependent and persistent in yellow monkeyflower (Mimulus guttatus)
inferredcites →https://doi.org/10.1093/hmg/ddi114openalex-snapshot
Epigenetic reprogramming in mammals
inferredcites →https://doi.org/10.1093/icb/icm061openalex-snapshot
Vive le difference! Sexual dimorphism and adaptive patterns in lizards of the genus Anolis
inferredcites →https://doi.org/10.1093/ilar.53.3-4.279openalex-snapshot
Epigenetic Influence of Stress and the Social Environment
inferredcites →https://doi.org/10.1093/oso/9780195111637.001.0001openalex-snapshot
Maternal Effects As Adaptations
inferredcites →https://doi.org/10.1095/biolreprod.104.030890openalex-snapshot
Maternal Diet and Other Factors Affecting Offspring Sex Ratio: A Review
inferredcites →https://doi.org/10.1098/rsbl.2005.0369openalex-snapshot
Trans-generational immune priming in a social insect
inferredcites →https://doi.org/10.1098/rsbl.2009.0754openalex-snapshot
Effects of parental larval diet on egg size and offspring traits in Drosophila
inferredcites →https://doi.org/10.1098/rsbl.2015.0472openalex-snapshot
Sex-specific maternal effects in a viviparous fish
inferredcites →https://doi.org/10.1098/rspb.1989.0027openalex-snapshot
Review Lecture: Mammalian mating systems
inferredcites →https://doi.org/10.1098/rspb.2002.2083openalex-snapshot
Sex-specific foraging behaviour in a monomorphic seabird
inferredcites →https://doi.org/10.1098/rspb.2004.3045openalex-snapshot
Stress-induced variation in evolution: from behavioural plasticity to genetic assimilation
inferredcites →https://doi.org/10.1098/rspb.2005.3274openalex-snapshot
Sex-specific effects of yolk testosterone on survival, begging and growth of zebra finches
inferredcites →https://doi.org/10.1098/rspb.2016.0988openalex-snapshot
DNA methylation mediates genetic variation for adaptive transgenerational plasticity
inferredcites →https://doi.org/10.1098/rstb.1991.0034openalex-snapshot
Clutch size, fecundity and parent-offspring conflict
inferredcites →https://doi.org/10.1098/rstb.2008.0137openalex-snapshot
Maternal transfer of antibodies in vertebrates: trans-generational effects on offspring immunity
inferredcites →https://doi.org/10.1098/rstb.2008.0237openalex-snapshot
Coping with environmental uncertainty: dynamic bet hedging as a maternal effect
inferredcites →https://doi.org/10.1098/rstb.2018.0181openalex-snapshot
Ancestral diet transgenerationally influences offspring in a parent-of-origin and sex-specific manner
inferredcites →https://doi.org/10.1101/763862openalex-snapshot
Sex-specific transgenerational plasticity I: Maternal and paternal effects on sons and daughters
inferredcites →https://doi.org/10.1101/791210openalex-snapshot
Transgenerational dispersal plasticity and its fitness consequences are under genetic control
inferredcites →https://doi.org/10.1111/1365-2435.12604openalex-snapshot
Transgenerational plasticity and environmental stress: do paternal effects act as a conduit or a buffer?
inferredcites →https://doi.org/10.1111/ele.12568openalex-snapshot
High fitness costs of climate change‐induced camouflage mismatch
inferredcites →https://doi.org/10.1111/evo.12635openalex-snapshot
When to rely on maternal effects and when on phenotypic plasticity?
inferredcites →https://doi.org/10.1111/evo.13403openalex-snapshot
Maternal effects and parent–offspring conflict
inferredcites →https://doi.org/10.1111/gcb.13903openalex-snapshot
Transgenerational plasticity and climate change experiments: Where do we go from here?
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00098.xopenalex-snapshot
SEXUAL DIMORPHISM IN RELATION TO CURRENT SELECTION IN THE HOUSE FINCH
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COSTS AND BENEFITS OF EVOLVING UNDER EXPERIMENTALLY ENFORCED POLYANDRY OR MONOGAMY
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Sexual selection, natural selection and quality advertisement
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Maternal and paternal condition effects on offspring phenotype inTelostylinus angusticollis(Diptera: Neriidae)
inferredcites →https://doi.org/10.1111/j.1420-9101.2011.02363.xopenalex-snapshot
Genetic variation for maternal effects on parasite susceptibility
inferredcites →https://doi.org/10.1111/j.1461-0248.2010.01537.xopenalex-snapshot
Evidence for trans‐generational medication in nature
inferredcites →https://doi.org/10.1111/j.1461-0248.2011.01721.xopenalex-snapshot
Thermal legacies: transgenerational effects of temperature on growth in a vertebrate
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ECOLOGICAL CAUSES OF SEXUAL DIMORPHISM
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01282.xopenalex-snapshot
A THEORETICAL MODEL OF THE EVOLUTION OF MATERNAL EFFECTS UNDER PARENT-OFFSPRING CONFLICT
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01704.xopenalex-snapshot
COMPLEX INTERACTIONS BETWEEN PATERNAL AND MATERNAL EFFECTS: PARENTAL EXPERIENCE AND AGE AT REPRODUCTION AFFECT FECUNDITY AND OFFSPRING PERFORMANCE IN A BUTTERFLY
inferredcites →https://doi.org/10.1111/j.2007.0030-1299.16203.xopenalex-snapshot
When is a maternal effect adaptive?
inferredcites →https://doi.org/10.1111/jeb.12212openalex-snapshot
Weak evidence for anticipatory parental effects in plants and animals
inferredcites →https://doi.org/10.1111/jeb.12872openalex-snapshot
Transgenerational effects of nutrition are different for sons and daughters
inferredcites →https://doi.org/10.1111/oik.01235openalex-snapshot
Adaptive parental effects: the importance of estimating environmental predictability and offspring fitness appropriately
inferredcites →https://doi.org/10.1126/science.1108190openalex-snapshot
Epigenetic Transgenerational Actions of Endocrine Disruptors and Male Fertility
inferredcites →https://doi.org/10.1126/science.1148766openalex-snapshot
Transgenerational Plasticity Is Adaptive in the Wild
inferredcites →https://doi.org/10.1126/science.1235765openalex-snapshot
Density Triggers Maternal Hormones That Increase Adaptive Offspring Growth in a Wild Mammal
inferredcites →https://doi.org/10.1126/science.155.3761.474openalex-snapshot
The Ecological Significance of Sexual Dimorphism in Size in the Lizard Anolis conspersus
inferredcites →https://doi.org/10.1126/science.289.5478.441openalex-snapshot
Evidence for Ecological Causation of Sexual Dimorphism in a Hummingbird
inferredcites →https://doi.org/10.1139/z85-148openalex-snapshot
The evolution of sexual dimorphism in the skink Eumeces laticeps: an example of sexual selection
inferredcites →https://doi.org/10.1155/2014/476917openalex-snapshot
Function and Regulation of the Plant COPT Family of High-Affinity Copper Transport Proteins
inferredcites →https://doi.org/10.1201/9781420065756.ch5openalex-snapshot
The Ecological And Evolutionary Importance Of Maternal Effects In The Sea
inferredcites →https://doi.org/10.1371/journal.pbio.1002469openalex-snapshot
Distinct Global Brain Dynamics and Spatiotemporal Organization of the Salience Network
inferredcites →https://doi.org/10.1523/jneurosci.3331-09.2009openalex-snapshot
The Epigenetics of Sex Differences in the Brain: Figure 1.
inferredcites →https://doi.org/10.1534/genetics.103.026211openalex-snapshot
Intralocus Sexual Conflict Can Drive the Evolution of Genomic Imprinting
inferredcites →https://doi.org/10.1890/09-1108.1openalex-snapshot
The ghosts of predators past: population cycles and the role of maternal programming under fluctuating predation risk
inferredcites →https://doi.org/10.2307/1935534openalex-snapshot
The Anolis Lizards of Bimini: Resource Partitioning in a Complex Fauna
inferredcites →https://doi.org/10.2307/2657035openalex-snapshot
The effect of maternal and paternal environments on seed characters in the herbaceous plant Campanula Americana (Campanulaceae)
inferredcites →https://doi.org/10.2307/3544525openalex-snapshot
The Ecological Correlates of Survival in Some Bahamian Anolis Lizards
inferredcites →https://doi.org/10.2307/3544943openalex-snapshot
Intraspecific Variation in Body Size and Fecundity in Insects: A General Relationship
inferredcites →https://doi.org/10.3354/meps311157openalex-snapshot
Stable isotopes indicate sex-specific and long-term individual foraging specialisation in diving seabirds
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ece3.9044openalex-snapshot
Parents exposed to warming produce offspring lower in weight and condition
inferred← citeshttps://doi.org/10.1007/s00442-022-05311-8openalex-snapshot
Maternal effects, paternal effects, and their interactions in the freshwater snail Physa acuta
inferred← citeshttps://doi.org/10.1007/s00442-025-05729-wopenalex-snapshot
Effects of selfing and outcrossing on transgenerational responses to predation risk
inferred← citeshttps://doi.org/10.1093/evolut/qpac051openalex-snapshot
Paternal condition affects offspring reproduction and life history in a sex-specific manner inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1098/rspb.2024.1037openalex-snapshot
Pesticide exposure triggers sex-specific inter- and transgenerational effects conditioned by past sexual selection
inferred← citeshttps://doi.org/10.1101/796995openalex-snapshot
Sex-specific transgenerational plasticity II: Grandpaternal effects are lineage- and sex-specific in threespined sticklebacks
inferred← citeshttps://doi.org/10.1111/1365-2435.13931openalex-snapshot
Nongenetic inheritance of behavioural variability is context specific and sex specific
inferred← citeshttps://doi.org/10.1111/1365-2656.13364openalex-snapshot
Sex‐specific plasticity across generations I: Maternal and paternal effects on sons and daughters
inferred← citeshttps://doi.org/10.1111/1365-2656.13365openalex-snapshot
Sex‐specific plasticity across generations II: Grandpaternal effects are lineage specific and sex specific
inferred← citeshttps://doi.org/10.1111/evo.14613openalex-snapshot
Evolutionary consequences of pesticide exposure include transgenerational plasticity and potential terminal investment transgenerational effects
inferred← citeshttps://doi.org/10.1111/mec.17328openalex-snapshot
Matching maternal and paternal experiences underpin molecular thermal acclimation
inferred← citeshttps://doi.org/10.3389/fevo.2020.548660openalex-snapshot
Transgenerational Plasticity in the Context of Predator-Prey Interactions
inferred← citeshttps://doi.org/10.3389/fevo.2020.591074openalex-snapshot
Interactions Between Maternal, Paternal, Developmental, and Immediate Environmental Effects on Anti-predator Behavior of the Snail Physa acuta
inferred← citeshttps://doi.org/10.70675/2099790bz7e54z4e5czaa83z7eafce19e326openalex-snapshot
Caractérisation de la plasticité transgénérationnelle : le cas des défenses contre les prédateurs du gastéropode Physa acuta
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