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      Coordinated response of endemic gastropods to Late Glacial and Holocene climate-driven paleohydrological changes in a small thermal pond of Central Europe

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      Scientific Reports
      Nature Publishing Group UK
      Evolution, Palaeontology, Limnology

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          Abstract

          The thermal spring-fed Lake Pețea located in NW Romania southeast of the city of Oradea harbors a unique endemic warm water biota. It is the only location in Europe where thermal water endemic melanopsid Microcolpia parreyssii (Philippi, 1847) lived along with the highly endangered warm-water relict neritid Theodoxus prevostianus. Lake Petea’s evolution was mainly controlled by major climate-driven hydrological changes also seen in regional records. The hydrological changes were mainly controlled by varying input of thermal water due to recurring increased/decreased recharge of the underground karst water system. The driving factor was warming connected to the interstadial GI 1 increasing recharge by melting of regional ice sheets in the Late Glacial. Conversely, during the Younger Dryas (H0) and the Holocene increasing/decreasing moisture availability was in control. Low stands created multiple bottlenecks reducing genetic variability seen in the appearance of extreme morphologies during next rapid climate melioration. The studied gastropods responded mostly similarly to changes controlling the availability of elements in shell construction and habitat reduction leading to changes in shape, density, size. Periods of lower lake levels and reduced warm water input are characterized by the emergence of elongated tightly coiled shells while globular, compressed loosely coiled shells develop at times of warmer water provision and increased Mg availability. In size there is a contrasting trend. Namely globose Th. prevostianus shells are larger than the elongated ones. Conversely globose, compressed Microcolpia are generally smaller than their elongated spindle-shaped counterparts. In this sense the development of dwarf morphotypes in warmer water habitats is characteristic of Lake Pețea melanopsids. This type of dwarfism i.e. the reduction of shell size is lacking though in Lake Pețea neritids. Our findings also confirm the presence of various ecophenotypes of Microcolpia in the pond degrading our endemic species Mi. parreyssii to a variety of Mi. daudebartii.

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          Developmental Plasticity and Evolution

          The first comprehensive synthesis on development and evolution: it applies to all aspects of development, at all levels of organization and in all organisms, taking advantage of modern findings on behavior, genetics, endocrinology, molecular biology, evolutionary theory and phylogenetics to show the connections between developmental mechanisms and evolutionary change. This book solves key problems that have impeded a definitive synthesis in the past. It uses new concepts and specific examples to show how to relate environmentally sensitive development to the genetic theory of adaptive evolution and to explain major patterns of change. In this book development includes not only embryology and the ontogeny of morphology, sometimes portrayed inadequately as governed by "regulatory genes," but also behavioral development and physiological adaptation, where plasticity is mediated by genetically complex mechanisms like hormones and learning. The book shows how the universal qualities of phenotypes--modular organization and plasticity--facilitate both integration and change. Here you will learn why it is wrong to describe organisms as genetically programmed; why environmental induction is likely to be more important in evolution than random mutation; and why it is crucial to consider both selection and developmental mechanism in explanations of adaptive evolution. This book satisfies the need for a truly general book on development, plasticity and evolution that applies to living organisms in all of their life stages and environments. Using an immense compendium of examples on many kinds of organisms, from viruses and bacteria to higher plants and animals, it shows how the phenotype is reorganized during evolution to produce novelties, and how alternative phenotypes occupy a pivotal role as a phase of evolution that fosters diversification and speeds change. The arguments of this book call for a new view of the major themes of evolutionary biology, as shown in chapters on gradualism, homology, environmental induction, speciation, radiation, macroevolution, punctuation, and the maintenance of sex. No other treatment of development and evolution since Darwin's offers such a comprehensive and critical discussion of the relevant issues. Developmental Plasticity and Evolution is designed for biologists interested in the development and evolution of behavior, life-history patterns, ecology, physiology, morphology and speciation. It will also appeal to evolutionary paleontologists, anthropologists, psychologists, and teachers of general biology.
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            Developmental plasticity and the origin of species differences.

            Speciation is the origin of reproductive isolation and divergence between populations, according to the "biological species concept" of Mayr. Studies of reproductive isolation have dominated research on speciation, leaving the origin of species differences relatively poorly understood. Here, I argue that the origin of species differences, and of novel phenotypes in general, involves the reorganization of ancestral phenotypes (developmental recombination) followed by the genetic accommodation of change. Because selection acts on phenotypes, not directly on genotypes or genes, novel traits can originate by environmental induction as well as mutation, then undergo selection and genetic accommodation fueled by standing genetic variation or by subsequent mutation and genetic recombination. Insofar as phenotypic novelties arise from adaptive developmental plasticity, they are not "random" variants, because their initial form reflects adaptive responses with an evolutionary history, even though they are initiated by mutations or novel environmental factors that are random with respect to (future) adaptation. Change in trait frequency involves genetic accommodation of the threshold or liability for expression of a novel trait, a process that follows rather than directs phenotypic change. Contrary to common belief, environmentally initiated novelties may have greater evolutionary potential than mutationally induced ones. Thus, genes are probably more often followers than leaders in evolutionary change. Species differences can originate before reproductive isolation and contribute to the process of speciation itself. Therefore, the genetics of speciation can profit from studies of changes in gene expression as well as changes in gene frequency and genetic isolation.
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              An event stratigraphy for the Last Termination in the North Atlantic region based on the Greenland ice-core record: a proposal by the INTIMATE group

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                Author and article information

                Contributors
                gulyas.sandor@geo.u-szeged.hu , csigonc@gmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                24 April 2024
                24 April 2024
                2024
                : 14
                : 9419
                Affiliations
                Department of Geology and Paleontology, University of Szeged, ( https://ror.org/01pnej532) Szeged, Hungary
                Article
                60185
                10.1038/s41598-024-60185-5
                11043081
                38658697
                bd36b815-9147-41b4-950e-1baf19960f97
                © The Author(s) 2024

                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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 February 2024
                : 19 April 2024
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100011019, Nemzeti Kutatási Fejlesztési és Innovációs Hivatal;
                Award ID: 129265
                Funded by: FundRef http://dx.doi.org/10.13039/501100012550, Nemzeti Kutatási, Fejlesztési és Innovaciós Alap;
                Award ID: 20391-3/2018/FEKUSTRAT
                Funded by: FundRef http://dx.doi.org/10.13039/501100015763, Szegedi Tudományegyetem;
                Award ID: Open Acess Fund 6951
                Award Recipient :
                Funded by: University of Szeged
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                © Springer Nature Limited 2024

                Uncategorized
                evolution,palaeontology,limnology
                Uncategorized
                evolution, palaeontology, limnology

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