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  • 1
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Evolution (Biology). ; Parthenogenesis in animals. ; Evolution, Molecular. ; Parthenogenesis. ; Evolution. ; Jungfernzeugung. ; Ungeschlechtliche Fortpflanzung. ; Aufsatzsammlung. ; Electronic books.
    Description / Table of Contents: Sex is still evolutionary biology's biggest paradox. This book gathers contributions from key researchers exploring asexual evolution in eukaryotes. It is a milestone in research on parthenogenesis and will be useful to students and researchers at all levels.
    Type of Medium: Online Resource
    Pages: 1 online resource (616 pages)
    Edition: 1st ed.
    ISBN: 9789048127702
    DDC: 576.8
    Language: English
    Note: Intro -- Foreword -- References -- Contents -- Contributors -- 1 Asex and Evolution: A Very Large-Scale Overview -- 1.1 Eukaryote Reproduction and the Meiotic Cycle -- 1.2 Asex Is Often Associated with Polyploidy and Hybridity -- 1.3 Asex Can Have Many Different Immediate Causes -- 1.4 Asex Is the Outcome of a Darwinian Process with Special Properties -- 1.5 Asex Is Almost Always Associated with Some Sex -- 1.6 Most Asexuals Are Genetically Variable -- 1.7 Asexual Lineages Are Comparatively Short-Lived -- 1.8 The Lack of Recombination Gives Asexual Lineages a Long-Term Disadvantage -- 1.9 The Paradox of Asex -- References -- 2 The Evolution of the Problem of Sex -- 2.1 Introduction -- 2.2 Darwin: The Effects of Cross-Fertilization -- 2.2.1 The Early Notebooks: Becoming Interested in the Significance of Sex -- 2.2.2 Sex and Variation -- 2.2.3 Sex Unites a Species -- 2.2.4 Cross-Fertilization: A Law of Nature -- 2.2.5 Sex and Hybrid Vigor -- 2.3 Weismann: The Significance of Sexual Reproduction in the Theory of Natural Selection -- 2.3.1 The Principles of Heredity -- 2.3.2 Heredity, Variability and Sex -- 2.3.3 The Significance of Sex, 1886 -- 2.3.4 The Significance of Sex, 1891 -- 2.3.5 Cyclical and Obligate Parthenogenesis -- 2.4 Fisher: The Contrast Between Sexual and Asexual Reproduction -- 2.4.1 Mendelism and Darwinism -- 2.4.2 The Adaptive Significance of Sex -- 2.4.3 Sex, Time and Levels of Selection -- 2.5 Maynard Smith: The Cost of Sex -- 2.5.1 The Evolutionary Synthesis and Appearing Complexities -- 2.5.2 Group Selection and Sex -- 2.5.3 The Fisher-Muller Model and a Changing Environment -- 2.5.4 The Problem of the Cost of Sex -- 2.5.5 Conceptual Framework -- 2.6 Discussion -- References -- 3 Apomixis: Basics for Non-botanists -- 3.1 Introduction -- 3.2 Vegetative Reproduction in Plants is Not Apomixis. , 3.3 Apomixis Is a Modification of Sexual Reproduction -- 3.4 Types of Apomixis in Flowering Plants -- 3.5 Pseudogamy and Autonomous Endosperm Development -- 3.6 Phenotyping Apomixis -- 3.7 Facultative Apomixis -- 3.8 Causes of Apomixis -- 3.9 Most Apomictic Plants Are Hermaphrodites -- 3.10 Somatic Mutations -- 3.11 The Phylogenetic Distribution of Apomixis in the Flowering Plants -- 3.12 Constraints on the Evolution of Apomixis in Flowering Plants -- 3.13 Ancient Apomicts in Flowering Plants -- 3.14 Further Reading -- 3.15 Glossary -- References -- 4 Cytology of Asexual Animals -- 4.1 The Importance of Cytology -- 4.2 Cytological Mechanisms of Animal Parthenogenesis -- 4.2.1 Automictic Parthenogenesis -- 4.2.1.1 Gamete Duplication -- 4.2.1.2 Terminal Fusion -- 4.2.1.3 Central Fusion -- 4.2.1.4 The First Polar Nucleus Fuses with the Nucleus of the Secondary Oocyte -- 4.2.1.5 Gonoid Thelytoky -- 4.2.1.6 Premeiotic Doubling -- 4.2.2 Apomictic Parthenogenesis -- 4.3 Evolutionary Consequences -- 4.4 Polyploidy in Association with Parthenogenesis -- 4.5 Conclusions -- References -- 5 A Graphical Approach to Lineage Selection Between Clonals and Sexuals -- 5.1 Introduction -- 5.2 Costs and Benefits of Sexual vs Clonal Reproduction -- 5.2.1 Short-Term Costs of Sexual Reproduction -- 5.2.2 Long-Term Costs of Clonal Reproduction -- 5.3 Fundamental Benefits to Sex -- 5.3.1 Equilibrium Mutational Load in Clonal Lineages -- 5.3.2 Contrasting Equilibrium Mutational Load in Sexual and Clonal Lineages -- 5.3.3 A Graphical Depiction of Background-Trapping and the Accumulation of Favourable and Harmful Mutations -- 5.4 Clonal vs Sexual Lineages -- 5.5 Conclusions -- References -- 6 Geographical Parthenogenesis: General Purpose Genotypes and Frozen Niche Variation -- 6.1 Introduction -- 6.1.1 Adaptation at the Margins -- 6.2 General Purpose Genotype (GPG). , 6.2.1 Elevated Ploidy and Hybridity -- 6.2.2 Evidence for General Purpose Genotypes -- 6.3 Frozen Niche-Variation (FNV) -- 6.3.1 Evidence for Frozen Niche Variation -- 6.4 Evolution of Generalist Versus Specialist Clones -- 6.4.1 GPG and FNV Are Not Mutually Exclusive -- 6.5 Conclusions -- References -- 7 Sex and the Red Queen -- 7.1 Sex and the Red Queen Introduction -- 7.2 Assumptions and Predictions of the Model -- 7.2.1 Population Genetics -- 7.2.2 Infection Dynamics -- 7.3 Does It Work? -- 7.3.1 Geographical Distribution of Sex and Outcrossing -- 7.3.2 Frequency of Sex vs Frequency of Infection -- 7.3.3 Susceptibility to Infection -- 7.3.4 Rare Advantage -- 7.3.5 Parasitic Tracking of Common Host Genotypes -- 7.3.6 Parasite Local Adaptation -- 7.3.7 Molecular Evolution in Disease Resistance Loci -- 7.4 Pluralism -- 7.4.1 The Red Queen and Pluralism -- 7.4.2 Empirical Tests -- 7.5 Conclusions -- References -- 8 Geographical Parthenogenesis: Opportunities for Asexuality -- 8.1 Introduction -- 8.2 The Main Current Hypotheses -- 8.3 The Connection of Polyploidy, Hybridization and Asexuality -- 8.4 Hybridization and Polyploidy, and the Cost of Origins of Asexuality -- 8.5 Climatic Changes as Opportunities for Origins and Dispersal of Asexuality -- 8.6 Case Studies in Ranunculus -- 8.7 Suggestions for Future Research -- 8.8 Glossary -- References -- 9 The Elusive Clone In Search of Its True Nature and Identity -- 9.1 Box 9.1: Definitions of Sex and Asex -- 9.1 What Are Clones? -- 9.2 A Brief History of Clonal Concepts -- 9.3 Germline Versus Soma: The Weismannian Doctrine Revisited -- 9.4 Clonal Concepts -- 9.5 Box 9.2: Brief Description of Extant Clonal Concepts -- 9.5 Validity of the Clonal Concepts -- 9.6 Conclusions -- References -- 10 Asexual Speciation -- 10.1 The Importance of Asexual Species. , 10.2 General Theory of Speciation and Species in Asexuals -- 10.3 Criteria for Assigning Individuals to Species -- 10.3.1 The 4X Rule -- 10.3.2 Analysis of Branching Rates -- 10.4 Application to Bdelloid Rotifers -- 10.5 Application to Oribatid Mites -- 10.6 Predictions About Relative Speciation Rates in Sexuals and Parthenogens -- 10.7 Conclusions -- References -- 11 Darwinulid Ostracods: Ancient Asexual Scandals or Scandalous Gossip? -- 11.1 Introduction -- 11.2 Box 11.1 Ostracoda -- 11.2 Ostracods in General -- 11.2 Ostracod Diversity -- 11.2 Reproductive Modes in Ostracods -- 11.2 Ecology of Darwinulidae -- 11.2 Life History of Darwinulidae -- 11.2 Demonstrating the Status of Long-Lived Asexuals -- 11.2.1 Recent Males -- 11.2.2 Fossil Males -- 11.2.3 Genetic Signatures of Ancient Asexuality: The Meselson-White Effect -- 11.2.4 Genomics: Transposons -- 11.2.5 Chromosomal Evidence: Aneuploidy -- 11.2.6 Ancient Asexual Status for Darwinulid Ostracods? -- 11.3 Ecological Strategies of Darwinulid Ostracods -- 11.3.1 GPG Versus FNV -- 11.3.2 Parasites or No Parasites? -- 11.3.3 Marginal Habitats and Long-Term Asexuality -- 11.3.4 Reduced Mutation Rates -- 11.3.5 Brood Selection or Enhanced Fecundity? -- 11.4 How Darwinulids Could Have Survived Without Sex for Millions of Years -- 11.5 What Remains to be Discovered -- References -- 12 Parthenogenesis in Oribatid Mites (Acari, Oribatida): Evolution Without Sex -- 12.1 General Biological Aspects of Oribatid Mites -- 12.1.1 Overview -- 12.1.2 Geological Age -- 12.1.3 Population Density -- 12.1.4 Niche Differentiation and Feeding Biology -- 12.1.5 Functioning -- 12.2 Reproductive and Developmental Biology -- 12.2.1 General Aspects -- 12.2.2 Female System and Reproductive Strategies -- 12.2.3 Parthenogenesis -- 12.2.4 Endosymbiotic Bacteria -- 12.3 Phylogeny of Parthenogenetic Lineages. , 12.3.1 General Phylogeny -- 12.3.2 Radiation of Parthenogenetic Lineages -- 12.4 Glossary -- References -- 13 Bdelloid Rotifers: Progress in Understanding the Success of an Evolutionary Scandal -- 13.1 Introduction -- 13.2 Evidence of Long-Term Asexuality in Bdelloidea -- 13.3 Environmental Adaptations in Bdelloidea -- 13.4 Anhydrobiosis -- 13.5 Ionizing Radiation and Desiccation -- 13.6 Genome Structure -- 13.7 Synthesis -- References -- 14 Sex Loss in Monogonont Rotifers -- 14.1 Introduction -- 14.2 The Monogonont Life Cycle -- 14.3 The Timing of Sex -- 14.4 The Cost of Sex in Cyclically Parthenogenetic Life Cycles -- 14.5 Mechanisms of Sex Loss in Monogononts -- 14.6 Selection for Sex Loss -- 14.7 Dormancy and Sex -- References -- 15 Cyclical Parthenogenesis in Daphnia : Sexual Versus Asexual Reproduction -- 15.1 Introduction -- 15.2 Cyclical Parthenogenesis and Its Effect on the Genetic Structure of Daphnia Populations -- 15.3 Reasons to Maintain Sexual Reproduction in Daphnia -- 15.3.1 Local Genetic Adaptation -- 15.3.2 Red Queen Dynamics -- 15.3.3 Deleterious Mutations -- 15.4 Evolution to Asexuality in Daphnia and Other Cladocerans -- 15.5 Why Switch to Asexual Reproduction When You Can Be a Cyclical Parthenogen? -- 15.5.1 Clonal Erosion and Inbreeding -- 15.5.2 Food Limitations and Time Stress -- 15.5.3 Genetic Slippage and Time Stress -- 15.5.4 Polyploidy and Hybrid Vigour -- 15.5.5 Contagious Asexuality: Selfish or Not? -- 15.6 Conclusions -- References -- 16 Metasexual Stick Insects: Model Pathways to Losing Sex and Bringing It Back -- 16.1 Introduction -- 16.1.1 Asexuals and Sexuals -- 16.1.2 Parthenogenesis and Polyploidy -- 16.2 Sexual and Asexual Stick Insects -- 16.2.1 Bacillus (Latreille) -- 16.2.2 Leptynia Pantel and Pijnackeria Scali -- 16.3 Centrosome Dynamics and -Tubulin(s) in Stick Insects. , 16.4 Conclusions Are Stick Insects True Asexuals?.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Freshwater biology 48 (2003), S. 0 
    ISSN: 1365-2427
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 〈list xml:id="l1" style="custom"〉1We investigated the relationship between geographical distribution and ecological tolerance within the ancient asexual family Darwinulidae. Distribution maps were compiled based on data from the literature, the Non-marine Ostracod Distribution in Europe database and personal collections. Ecological tolerance was assessed experimentally by exposing individual ostracods to a combination of eight different salinities (range from 0 to 30 g L−1) and three different temperatures (10, 20 and 30 °C).2The type species of the family, Darwinula stevensoni, is ubiquitous and cosmopolitan; the two species Penthesilenula brasiliensis and Microdarwinula zimmeri also have an intercontinental distribution. Two other darwinulid species tested here (Vestalenula molopoensis and P. aotearoa) are known only from their type localities. The latter is also true for most extant darwinulids.3 Darwinula stevensoni and P. brasiliensis had a broad salinity tolerance, tolerating distilled water and also salinity up to 25–30 g L−1, whereas the maximum salinity tolerance of V. molopoensis was 12 g L−1 and of P. aotearoa, 20 g L−1.4The results indicate that both ecological specialists and generalists, as well as intermediate forms, exist in the Darwinulidae and that taxa with the broadest ecological tolerance also have the widest distribution.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2023-02-08
    Description: In 2015, we have collected more than 60,000 scavenging amphipod specimens during two expeditions to the Clarion-Clipperton fracture Zone (CCZ), in the Northeast (NE) Pacific and to the DISturbance and re-COLonisation (DisCOL) Experimental Area (DEA), a simulated mining impact disturbance proxy in the Peru basin, Southeast (SE) Pacific. Here, we compare biodiversity patterns of the larger specimens (〉15mm) within and between these two oceanic basins. Nine scavenging amphipod species are shared between these two areas, thus indicating connectivity. We further provide evidence that disturbance proxies seem to negatively affect scavenging amphipod biodiversity, as illustrated by a reduced alpha biodiversity in the DEA (Simpson Index (D)=0.62), when compared to the CCZ (D=0.73) and particularly of the disturbance site in the DEA and the site geographically closest to it. Community compositions of the two basins differs, as evidenced by a Non-Metric Dimensional Scaling (NMDS) analysis of beta biodiversity. The NMDS also shows a further separation of the disturbance site (D1) from its neighbouring, undisturbed reference areas (D2, D3, D4 and D5) in the DEA. A single species, Abyssorchomene gerulicorbis, dominates the DEA with 60% of all individuals.
    Type: Article , PeerReviewed
    Format: text
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  • 4
    Publication Date: 2024-01-14
    Description: Severe storm flooding poses a major hazard to the coasts of north‐western Europe. However, the long‐term recurrence patterns of extreme coastal flooding and their governing factors are poorly understood. Therefore, high‐resolution sedimentary records of past North Atlantic storm flooding are required. This multi‐proxy study reconstructs storm‐induced overwash processes from coastal lake sediments on the Shetland Islands using grain‐size and geochemical data, and the re‐analysis of historical data. The chronostratigraphy is based on Bayesian age–depth modelling using accelerator mass spectrometry 14 C and 137 Cs data. A high XRF‐based Si/Ti ratio and the unimodal grain‐size distribution link the sand layers to the beach and thus storm‐induced overwash events. Periods with more frequent storm flooding occurred 980–1050, 1150–1300, 1450–1550, 1820–1900 and 1950–2000 ce, which is largely consistent with a positive North Atlantic Oscillation mode. The Little Ice Age (1400–1850 ce ) shows a gap of major sand layers suggesting a southward shift of storm tracks and a seasonal variance with more storm floods in spring and autumn. Warmer phases shifted winter storm tracks towards the north‐east Atlantic, indicating a possible trend for future storm‐track changes and increased storm flooding in the northern North Sea region.
    Type: Article , PeerReviewed
    Format: text
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