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      Extreme thermal fluctuations from climate change unexpectedly accelerate demographic collapse of vertebrates with temperature-dependent sex determination

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          Abstract

          Global climate is warming rapidly, threatening vertebrates with temperature-dependent sex determination (TSD) by disrupting sex ratios and other traits. Less understood are the effects of increased thermal fluctuations predicted to accompany climate change. Greater fluctuations could accelerate feminization of species that produce females under warmer conditions (further endangering TSD animals), or counter it (reducing extinction risk). Here we use novel experiments exposing eggs of Painted Turtles ( Chrysemys picta) to replicated profiles recorded in field nests plus mathematically-modified profiles of similar shape but wider oscillations, and develop a new mathematical model for analysis. We show that broadening fluctuations around naturally male-producing (cooler) profiles feminizes developing embryos, whereas embryos from warmer profiles remain female or die. This occurs presumably because wider oscillations around cooler profiles expose embryos to very low temperatures that inhibit development, and to feminizing temperatures where most embryogenesis accrues. Likewise, embryos incubated under broader fluctuations around warmer profiles experience mostly feminizing temperatures, some dangerously high (which increase mortality), and fewer colder values that are insufficient to induce male development. Therefore, as thermal fluctuations escalate with global warming, the feminization of TSD turtle populations could accelerate, facilitating extinction by demographic collapse. Aggressive global CO 2 mitigation scenarios (RCP2.6) could prevent these risks, while intermediate actions (RCP4.5 and RCP6.0 scenarios) yield moderate feminization, highlighting the peril that insufficient reductions of greenhouse gas emissions pose for TSD taxa. If our findings are generalizable, TSD squamates, tuatara, and crocodilians that produce males at warmer temperatures could suffer accelerated masculinization, underscoring the broad taxonomic threats of climate change.

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          Sex reversal triggers the rapid transition from genetic to temperature-dependent sex.

          Sex determination in animals is amazingly plastic. Vertebrates display contrasting strategies ranging from complete genetic control of sex (genotypic sex determination) to environmentally determined sex (for example, temperature-dependent sex determination). Phylogenetic analyses suggest frequent evolutionary transitions between genotypic and temperature-dependent sex determination in environmentally sensitive lineages, including reptiles. These transitions are thought to involve a genotypic system becoming sensitive to temperature, with sex determined by gene-environment interactions. Most mechanistic models of transitions invoke a role for sex reversal. Sex reversal has not yet been demonstrated in nature for any amniote, although it occurs in fish and rarely in amphibians. Here we make the first report of reptile sex reversal in the wild, in the Australian bearded dragon (Pogona vitticeps), and use sex-reversed animals to experimentally induce a rapid transition from genotypic to temperature-dependent sex determination. Controlled mating of normal males to sex-reversed females produces viable and fertile offspring whose phenotypic sex is determined solely by temperature (temperature-dependent sex determination). The W sex chromosome is eliminated from this lineage in the first generation. The instantaneous creation of a lineage of ZZ temperature-sensitive animals reveals a novel, climate-induced pathway for the rapid transition between genetic and temperature-dependent sex determination, and adds to concern about adaptation to rapid global climate change.
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            Environmental Warming and Feminization of One of the Largest Sea Turtle Populations in the World

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              Plasticity and genetic adaptation mediate amphibian and reptile responses to climate change

              Phenotypic plasticity and genetic adaptation are predicted to mitigate some of the negative biotic consequences of climate change. Here, we evaluate evidence for plastic and evolutionary responses to climate variation in amphibians and reptiles via a literature review and meta-analysis. We included studies that either document phenotypic changes through time or space. Plasticity had a clear and ubiquitous role in promoting phenotypic changes in response to climate variation. For adaptive evolution, we found no direct evidence for evolution of amphibians or reptiles in response to climate change over time. However, we found many studies that documented adaptive responses to climate along spatial gradients. Plasticity provided a mixture of adaptive and maladaptive responses to climate change, highlighting that plasticity frequently, but not always, could ameliorate climate change. Based on our review, we advocate for more experiments that survey genetic changes through time in response to climate change. Overall, plastic and genetic variation in amphibians and reptiles could buffer some of the formidable threats from climate change, but large uncertainties remain owing to limited data.
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                Author and article information

                Contributors
                nvalenzu@iastate.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                12 March 2019
                12 March 2019
                2019
                : 9
                : 4254
                Affiliations
                [1 ]ISNI 0000 0004 1936 7312, GRID grid.34421.30, Department of Ecology, Evolution and Organismal Biology, , Iowa State University, ; Ames, IA 50011 USA
                [2 ]ISNI 0000 0004 1936 8083, GRID grid.47894.36, Present Address: Department of Biology, , Colorado State University, ; Fort Collins, CO 80523 USA
                [3 ]ISNI 0000 0001 1960 0522, GRID grid.255360.7, Department of Biology, , Earlham College, ; Richmond, Indiana 47374 USA
                [4 ]ISNI 0000 0001 2214 904X, GRID grid.11956.3a, Present Address: Department of Botany and Zoology, , Stellenbosch University, ; Matieland, 7602, Stellenbosch, Western Cape 7600 South Africa
                [5 ]ISNI 0000 0004 0469 5874, GRID grid.258970.1, Department of Biology, , Laurentian University, ; Sudbury, Ontario P3E 2C6 Canada
                Author information
                http://orcid.org/0000-0003-1148-631X
                Article
                40597
                10.1038/s41598-019-40597-4
                6414666
                30626917
                afe6cbf7-b520-44f4-99ab-2c703faddc90
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 6 June 2018
                : 20 February 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/100000154, NSF | BIO | Division of Integrative Organismal Systems (IOS);
                Award ID: IOS-0743284
                Award ID: IOS-1555999
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000152, NSF | BIO | Division of Molecular and Cellular Biosciences (MCB);
                Award ID: MCB-0815354
                Award ID: MCB-1244355
                Award Recipient :
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