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  • 1
    Online Resource
    Online Resource
    Cary :Oxford University Press, Incorporated,
    Keywords: Generative organs -- Evolution. ; Sexual selection in animals. ; Electronic books.
    Description / Table of Contents: This edited volume explores primary sexual characters in a wide variety of animal taxa. It provides an overview of sexual diversity, the selective pressures that have shaped it, and an introduction to the data and theoretical issues in sexual selection that are changing our view of sexual processes.
    Type of Medium: Online Resource
    Pages: 1 online resource (550 pages)
    Edition: 1st ed.
    ISBN: 9780199717033
    DDC: 591.56/2
    Language: English
    Note: Intro -- Contents -- Contributors -- 1. Introduction: Celebrating and Understanding Reproductive Diversity -- Part I: General Considerations -- 2. The Distinction between Primary and Secondary Sexual Characters -- 3. The Evolution of Sexes, Anisogamy, and Sexual Systems: Natural versus Sexual Selection -- 4. Rapid Divergent Evolution of Genitalia: Theory and Data Updated -- 5. Killing Time: A Mechanism of Sexual Conflict and Sexual Selection -- Part II: Primary Sexual Characters in Selected Taxa -- 6. Gamete Release and Spawning Behavior in Broadcast Spawning Marine Invertebrates -- 7. Prosobranchs with Internal Fertilization -- 8. Opisthobranchs -- 9. Basommatophoran Gastropods -- 10. Stylommatophoran Gastropods -- 11. An Ancient Indirect Sex Model: Single and Mixed Patterns in the Evolution of Scorpion Genitalia -- 12. Spider Genitalia: Precise Maneuvers with a Numb Structure in a Complex Lock -- 13. Genitalic Evolution in Opiliones -- 14. The Evolution of Male and Female Internal Reproductive Organs in Insects -- 15. Selective Forces Propelling Genitalic Evolution in Odonata -- 16. Postcopulatory Sexual Selection in the Coleoptera: Mechanisms and Consequences -- 17. Fertilization Mode, Sperm Competition, and Cryptic Female Choice Shape Primary Sexual Characters in Fish -- 18. Evolution of Primary Sexual Characters in Amphibians -- 19. Evolution of Primary Sexual Characters in Reptiles -- 20. Sexual Conflict and the Intromittent Organs of Male Birds -- 21. Genitalic Traits of Mammals: Systematics and Variation -- 22. The Evolution of Primary Sexual Characters in Animals: A Summary -- Index -- A -- B -- C -- D -- E -- F -- G -- H -- I -- J -- K -- L -- M -- N -- O -- P -- Q -- R -- S -- T -- U -- V -- W -- X -- Y -- Z.
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  • 2
    Online Resource
    Online Resource
    Oxford :Oxford University Press, Incorporated,
    Keywords: Insects-Evolution. ; Damselflies. ; Dragonflies. ; Electronic books.
    Description / Table of Contents: Documents the latest advances in odonate biology and relates these to a broader ecological and evolutionary research agenda. A diverse set of contributions from many of the leading researchers in dragonfly biology offer fresh perspectives and new paradigms as well as additional, unpublished data.
    Type of Medium: Online Resource
    Pages: 1 online resource (484 pages)
    Edition: 2nd ed.
    ISBN: 9780192653802
    DDC: 595.733
    Language: English
    Note: Cover -- Dragonflies and Damselflies: Model Organisms for Ecological and Evolutionary Research -- Copyright -- List of Contributors -- List of Reviewers -- Contents -- Foreword -- 1 Introduction to Dragonflies and Damselflies, Second Edition -- SECTION 1 Genomics SECTION EDITOR: Alex Córdoba-Aguilar -- 2 Genomic insights into micro- and macro-evolutionary processes in Odonata -- 2.1 Introduction -- 2.2 Genomic insights into population processes -- 2.2.1 Dispersal and connectivity -- 2.2.2 Range shifts and other spatial processes -- 2.3 Adaptation and adaptive trait evolution -- 2.3.1 Environmental adaptation -- 2.3.2 Morphological adaptation -- 2.3.3 Life stage-specific adaptation -- 2.4 Genomic variation associated with hybridization and speciation -- 2.4.1 Insights from genome assemblies into species- and order-specific functional traits -- 2.5 Conclusions and future directions -- References -- 3 Transcriptomic insights into Odonata ecology and evolution -- 3.1 Introduction -- 3.2 Color vision -- 3.3 Transcriptomic insight into the eco-evolutionary role of color variation -- 3.3.1 Ecological significance of color variation within and between species -- 3.3.2 Evolution of color phenotypes -- 3.3.3 Pigments -- 3.3.4 Structural colors -- 3.3.5 Genes involved in body color formation -- 3.4 Embryogenesis -- 3.4.1 Gene expression during embryogenesis -- 3.5 Phylo-transcriptomics -- 3.6 Future directions -- 3.6.1 Color vision -- 3.6.2 Color -- 3.6.3 Embryogenesis -- 3.6.4 Phylogenomics -- 3.7 Conclusion -- Acknowledgments -- References -- SECTION 2 Organismal Studies -- 4 Functional morphology in Odonata -- 4.1 Introduction -- 4.2 Head -- 4.3 Head-thorax articulation -- 4.4 Thorax -- 4.5 Wings -- 4.6 Legs -- 4.7 Abdomen -- Method Boxes -- References -- 5 The biomechanics of odonate flight -- 5.1 Flight mechanics -- 5.2 Muscle activation. , 5.3 Wing structure -- 5.4 Flapping wing aerodynamics -- 5.4.1 Leading-edge vortex -- 5.4.2 Stroke plane -- 5.4.3 Planform -- 5.5 Aerodynamic interactions -- 5.5.1 Wing phasing -- 5.6 Flight control and sensing -- 5.6.1 Passive control -- 5.6.2 Active control -- 5.6.3 Predicting sensory inputs -- 5.7 Concluding remarks -- Acknowledgments -- References -- 6 Odonata immunity, pathogens, and parasites -- 6.1 Introduction -- 6.2 Parasites -- 6.2.1 Viruses -- 6.2.2 Bacteria -- 6.2.3 Gregarines -- 6.2.4 Trematodes -- 6.2.5 Water mites -- 6.2.6 Parasitoids -- 6.2.7 Coinfection -- 6.3 Odonate immunity -- 6.3.1 Overview of insect immunity -- 6.3.2 Components of odonate immunity -- 6.4 Ecology and evolution of immunity and parasites -- 6.4.1 PO and food webs -- 6.4.2 Metacommunity structure -- 6.4.3 Coevolution -- 6.5 Future research directions -- 6.5.1 Genetics -- 6.5.2 Microbiome -- 6.5.3 Climate change -- 6.6 Conclusions -- Acknowledgments -- References -- 7 Odonata perception is more than vision -- 7.1 Introduction -- 7.2 Adult -- 7.2.1 Antennae -- 7.2.2 Mouthparts and gustatory sensilla -- 7.2.3 The ovipositor sensilla: sensing the plant taste and stiffness -- 7.3 Nymph -- 7.3.1 Antennae -- 7.4 Conclusions and future perspectives -- References -- 8 Thermoregulation in Odonata -- 8.1 Introduction -- 8.2 Mechanisms of thermoregulation -- 8.2.1 Ectothermy and behavior -- 8.2.2 Ectothermy and color -- 8.2.3 Endothermy -- 8.3 Global change and thermal limits -- 8.4 Global change and body coloration -- 8.5 Odonate resilience: a link to thermoregulation? -- 8.6 Linking thermoregulation mechanisms to global temperature changes -- 8.7 Some topics for future thermoregulation research -- 8.7.1 Genetics and physiology of thermoregulation -- 8.7.2 Mechanisms of thermoregulation -- 8.7.3 Trade-offs between thermoregulation and other functions. , 8.7.4 Human awareness via insect thermoregulation risk under climate change -- Acknowledgments -- References -- SECTION 3 Population Ecology: Christopher D. Beatty -- 9 Genetic structure, cryptic species, and hybridization causes and evolutionary consequences in Odonata -- 9.1 Introduction -- 9.2 Gene flow within species: population genetic structure in odonates -- 9.3 Cryptic species in odonates -- 9.4 Gene flow between species: hybridization in odonates -- 9.5 Conclusions and research directions -- Acknowledgments -- References -- 10 Odonata survival -- 10.1 Introduction -- 10.2 The effect of marking -- 10.3 A review of the literature using marking methods with odonates -- 10.4 The effect of sex and age on survival and recapture rates -- 10.5 The effect of female color polymorphism -- 10.6 Individual and environmental covariates -- 10.7 Conclusions and further research -- Acknowledgments -- References -- 11 Migration in Anisoptera -- 11.1 Introduction -- 11.2 Migratory case studies in odonates -- 11.2.1 Anax junius -- 11.2.2 Pantala flavescens -- 11.3 Migration and weather -- 11.4 Migration and reproduction -- 11.5 Population studies in migrating dragonflies -- 11.6 Migrants vs. residents-how might they evolve? -- 11.7 Future directions -- Acknowledgments -- References -- 12 Dispersal and metapopulation ecology in Odonata -- 12.1 Dispersal biology in ecology and evolution -- 12.2 Dispersal biology in Odonata -- 12.3 Methods for studying dispersal in odonates -- 12.4 Dispersal and population structure -- 12.4.1 Context- and phenotype-dependent dispersal -- 12.4.2 Spatially structured populations -- 12.4.3 Dispersal and species ranges -- 12.5 Dispersal and colonization in the Anthropocene -- 12.5.1 Effects of human alteration of matrix environments on dispersal and habitat colonization -- 12.5.2 Colonization and ecological traps. , 12.6 Future research directions in the study of dispersal in Odonata -- 12.6.1 Dispersal in the context of anthropogenic change -- 12.6.2 Rapidly advancing methods -- 12.6.3 Research across a greater diversity of the world's landscapes -- Acknowledgments -- References -- 13 Biogeographical ecology in Odonata -- 13.1 Introduction to biogeography -- 13.1.1 Biogeographical concepts through history -- 13.1.2 Historical and ecological biogeography -- 13.2 Biogeographic realms and odonate species distributions -- 13.2.1 Nearctic -- 13.2.2 Palearctic -- 13.2.3 Indo-Malayan -- 13.2.4 Australasia -- 13.2.5 Oceanic-Pacific -- 13.2.6 Afrotropics -- 13.2.7 Neotropics -- 13.3 Factors influencing odonate distributions -- 13.3.1 Climatic factors -- 13.3.2 Precipitation -- 13.3.3 Temperature -- 13.3.4 Tracking suitable climates: differences in temperature causes different species compositions -- 13.3.5 Geographic barriers -- 13.3.6 Mountains and plains -- 13.3.7 River basins -- 13.3.8 Glaciation patterns -- 13.4 Considerations of scale in odonate biogeographical analysis -- 13.5 Life history evolution in odonate biogeography -- 13.5.1 Latitudinal differences in voltinism -- 13.5.2 Latitudinal patterns in thermal adaptation and space-for-time substitution studies -- 13.6 Conservation Biogeography -- 13.7 Future directions -- Acknowledgments -- References -- SECTION 4 Community Ecology -- 14 Evolutionary community ecology of Odonata -- 14.1 Introduction -- 14.2 Interactions in odonates -- 14.2.1 Predation-odonates as prey -- 14.2.2 Predation-odonates as predators -- 14.2.3 Competition -- 14.2.4 Parasitism -- 14.2.5 Reproductive interactions -- 14.3 Natural and sexual selection in communities -- 14.3.1 Selection in larvae -- 14.3.2 Selection in adults -- 14.4 Eco-evolutionary effects in communities -- 14.4.1 Adaptation to biotic interactions. , 14.4.2 Adaptation during range expansion -- 14.5 Future directions and conclusion -- Acknowledgments -- References -- 15 Ecological differentiation, interference, and coexistence in Odonata -- 15.1 Introduction -- 15.2 Coexistence theory -- 15.2.1 Local coexistence -- 15.2.2 Regional (non-local) coexistence -- 15.2.3 Interspecific interference and coexistence -- 15.2.4 Intraspecific interference and coexistence -- 15.3 Empirical studies on coexistence and competition in Odonata assemblages -- 15.3.1 Local coexistence -- 15.3.2 Regional coexistence -- 15.3.3 Exploitative competition among larvae -- 15.3.4 Interference competition among larvae -- 15.3.5 Interspecific aggressive and reproductive interference at the adult stage -- 15.3.6 Intraspecific interference at the adult stage -- 15.4 Conclusions and recommendations -- Acknowledgments -- References -- 16 Odonata trophic ecology from hunting behavior to cross-ecosystem impact -- 16.1 Introduction -- 16.2 Background to odonate trophic ecology -- 16.2.1 Trophic role of odonates in aquatic food webs -- 16.2.2 Odonate hunting behavior -- 16.2.3 Visual, chemical, and olfactory cues -- 16.3 Shifts and variation in odonate trophic relations -- 16.3.1 Ontogenetic scaling and trophic niche shifts -- 16.3.2 Sex differences in adult diet -- 16.3.3 Carryover effects of larval diet on adult phenotypic traits and fitness -- 16.3.4 Carryover effects of predation risk on adult traits -- 16.3.5 Metamorphosis and shifts from aquatic to terrestrial diets -- 16.4 Trophic and non-trophic interactions in food webs -- 16.4.1 Cannibalism and intraguild predation (IGP) -- 16.4.2 Non-trophic interactions -- 16.4.3 Trophic cascades and cross-ecosystem fluxes -- 16.5 Importance of abiotic factors in odonate trophic ecology -- 16.6 Eco-evolutionary dynamics of trophic interactions -- 16.7 Conclusions and research directions. , Acknowledgments.
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  • 3
    Online Resource
    Online Resource
    Oxford :Oxford University Press, Incorporated,
    Keywords: Insects-Behavior. ; Electronic books.
    Description / Table of Contents: This edited volume offers a new approach that will provide readers with the theoretical and conceptual foundations, at different hierarchical levels, to understand insect behavior.
    Type of Medium: Online Resource
    Pages: 1 online resource (410 pages)
    Edition: 1st ed.
    ISBN: 9780192518095
    DDC: 595.715
    Language: English
    Note: Cover -- Insect Behavior: From mechanisms to ecological and evolutionary consequences -- Copyright -- Foreword -- Acknowledgements -- Contents -- List of contributors -- CHAPTER 1: Introduction -- 1.1 Introduction -- References -- CHAPTER 2: The genetics of reproductivebehavior -- 2.1 Introduction -- 2.2 Reproductive behaviors in insects are polygenic and each gene has a small effect -- 2.2.1 Exploring genetic variation in insect reproductive behavior using quantitative genetics -- 2.2.2 Estimating genetic variance and heritability for phenotypic traits -- 2.2.3 Empirical evidence from quantitative genetics for the polygenic control of reproductive behaviors in insects -- 2.2.4 Revealing specific gene effects through quantitative trait loci mapping and 'omics' approaches -- 2.2.5 Identifying QTLs and candidate genes of interest for insect reproductive behavior -- 2.2.6 Empirical evidence from QTL-based studies examining the polygenic control of reproductive behaviors in insects -- 2.3 Genes that have a major effecton insect reproductive behavior: the exception to the polygenic rule -- 2.4 Genes for reproductive behavior areoften linked to other traits -- 2.4.1 Estimating genetic correlations between traits using quantitative genetics -- 2.4.2 Empirical examples of genetic correlations between reproductive behavior and other traits in insects -- 2.5 Genes can have non-additive effects on reproductive behavior -- 2.5.1 Estimating the effects of dominance and epistasis on phenotype using quantitative genetics -- 2.5.2 Empirical examples of non-additive genetic effects for insect reproductive behavior -- 2.6 Genes for reproductive behavior frequently interact with the environment -- 2.6.1 Estimating GEIs and GSEIs for phenotypic traits using quantitative genetics -- 2.6.2 Empirical examples of GEIs for insect reproductive behavior. , 2.7 Wider evolutionary implications and areas for future research on the genetic architecture of insect reproductive behavior -- References -- CHAPTER 3: Neurobiology -- 3.1 Methods in insect behavioral neurobiology -- 3.2 The insect nervous system -- 3.2.1 General structure -- 3.2.2 Neurons and glia -- 3.3 Control of behavior by characterized brain regions -- 3.3.1 Vision: optic lobes -- 3.3.2 Olfaction: antennal lobes -- 3.3.3 Integration and learning: mushroom bodies -- 3.3.4 Navigation and motor control: central complex -- 3.4 Metamorphosis and nervous system plasticity -- 3.4.1 Restructuring of the nervous system during metamorphosis -- 3.4.2 Plasticity of the adult nervous system -- 3.5 Case study: neurons and circuits for Drosophila sexual behavior -- Acknowledgement -- References -- CHAPTER 4: The role of hormones -- 4.1 Introduction -- 4.2 Behavior and hormonally-controlled life-stage transitions -- 4.3 Polyphenisms and behavior -- 4.4 Hormones, receptors, and sensitive periods -- 4.5 Hormonally-induced behaviors associated with moulting and metamorphosis -- 4.6 Hormones and migration -- 4.7 Hormonal control of pheromone production and mating activity -- 4.8 Hormones and parental care -- 4.9 Dominance and social behavior -- 4.10 Conclusions -- References -- CHAPTER 5: Phenotypic plasticity -- 5.1 Introduction -- 5.1.1 Phenotypic plasticity, genes, and environments, and their interaction -- 5.1.2 Sources of behavioral variability -- 5.2 Polyphenisms -- 5.2.1 Social context and polyphenisms -- 5.2.2 Nutritional context and polyphenisms -- 5.2.3 Seasonal context and polyphenisms -- Diapause -- Migration -- 5.3 Gene-by-environment interactions (GxE) -- 5.3.1 The Drosophila foraging gene model -- 5.3.2 Phenotypic plasticity and the Drosophila foraging gene -- 5.3.3 The foraging gene in eusocial insects -- 5.3.4 Pleiotropy and the foraging gene. , 5.3.5 Trade-offs -- Horned and hornless beetles -- Parasitoids -- 5.4 Potential molecular mechanisms of plasticity: behavioral epigenetics -- 5.5 Conclusions -- Acknowledgements -- References -- CHAPTER 6: Habitat selection and territoriality -- 6.1 Introduction -- 6.2 Adult sex roles and behavior -- 6.3 Mating habitats, site selection, and territoriality -- 6.3.1 The spatiotemporal basis of mating habitats -- 6.3.2 The occurrence and economics of site defence -- 6.3.3 Encounter site fidelity -- 6.3.4 Contest form -- 6.4 The logical basis of dyadic contests -- 6.4.1 Fighting ability, resource value, and motivation -- 6.4.2 The availability and assessment of information -- 6.4.3 Convention -- 6.5 The functional basis of competitive ability -- 6.5.1 An empirical framework -- 6.5.2 Physical determinants of RHP -- 6.5.3 Subjective RV and motivation -- 6.6 Residency and role-related phenomena -- 6.6.1 Residency-based convention -- 6.6.2 Contestant roles: know thy challenger? -- 6.6.3 Time-in-residency effects -- 6.6.4 Dear enemies or nasty neighbours? -- 6.7 Future research prospects -- References -- CHAPTER 7: Long-range migration and orientationbehavior -- 7.1 Introduction -- 7.2 What is migration? -- 7.2.1 The migration syndrome -- 7.2.2 A Holistic Model-the Migration System -- 7.3 Migration through the atmosphere -- 7.4 Orientation behavior of insect migrants -- 7.4.1 The initiation of migration and the orientation at take-off -- 7.4.2 Orientation in the 'transmigration' phase -- 7.4.3 The termination of migration: fallout and settling behavior -- 7.5 Some examples of long-range insect flight trajectories and population trajectories -- 7.6 Population consequences of migration -- 7.7 Environmental change and migration -- 7.8 Some outstanding questions and issues in insect migration behavior -- 7.9 Concluding remarks -- References. , CHAPTER 8: Feeding behavior -- 8.1 Introduction -- 8.2 Patterns of feeding: control of meals and inter-meal intervals -- 8.3 Automating the recording of feeding behavior -- 8.4 Regulation of multiple nutrient intakes -- 8.5 Physiological and molecular mechanisms of appetite in Drosophila -- 8.6 The geometric framework -- 8.7 Using the geometric framework to map the consequences of feeding behavior for individuals -- 8.8 Microbial associations, parasites, and immunity -- 8.9 Beyond the individual: social interactions -- 8.10 Trophic interactions and ecosystem dynamics -- 8.11 Contribution of insects beyond entomology -- 8.12 Conclusions -- Acknowledgements -- References -- CHAPTER 9: Anti-predator behavior -- 9.1 Overview -- 9.2 Some simple ways of classifying anti-predator defences -- 9.3 Anti-predator behavior as partof a primary defence -- 9.3.1 Seek (or create) a refuge -- 9.3.2 Micro-habitat selection -- 9.3.3 Behavioral mimicry -- 9.3.4 Warning displays -- 9.4 Anti-predator behavior when the primary defence fails -- 9.4.1 Flee -- 9.4.2 Startle defences -- 9.4.3 'Death feigning' (tonic immobility) -- 9.4.4 Fighting back -- 9.5 The comparative approach to understanding variation in anti-predator -- 9.6 Conclusions -- References -- CHAPTER 10: Chemical communication -- 10.1 What is communication? -- 10.2 What makes chemical communication special? -- 10.2.1 Specificity -- 10.2.2 Cost -- 10.2.3 Directionality -- 10.2.4 Speed -- 10.2.5 Persistence -- 10.2.6 Susceptibility to eavesdropping -- 10.2.7 Physical and energetic limits -- 10.2.8 Chemical diversity -- 10.3 The detection versus reliability problem -- 10.4 Chemical compounds as mediators of conflict and resolution -- 10.5 Honest signals -- 10.6 Deceptive signals -- 10.7 Chemical communication and higher-order processes -- 10.8 Conclusions -- References -- CHAPTER 11: Visual communication. , 11.1 Introduction -- 11.2 Physiology: structure and optics of the compound eye -- 11.3 Ecology: Senders, receivers, and signalling environments -- 11.3.1 Signal generation -- 11.3.2 Signal transmission -- 11.3.3 Signal reception and processing -- 11.4 Evolution: forms and function of visual communication -- 11.4.1 Visual communication between mates -- 11.4.2 Visual communication between rival conspecifics -- 11.4.3 Visual communication in cooperation among conspecifics -- 11.4.4 Protective signalling to avoid predation -- 11.5 Conclusion -- References -- CHAPTER 12: Acoustic communication -- 12.1 Introduction -- 12.2 The behavioral context for signalling -- 12.2.1 Mate attraction -- 12.2.2 Agonistic interactions between males -- 12.2.3 Spacing -- 12.2.4 Courtship -- 12.3 Signal production -- 12.3.1 Far-field sound -- 12.3.2 Near-field sound -- 12.3.3 Substrate vibration -- 12.4 The transmission channel forthe signal -- 12.4.1 Transmission of air-borne sound:geometric spreading, excess attenuation,and degradation of temporal cues -- 12.4.2 Noise in the air-borne sound channel -- 12.4.3 Transmission of substrate vibrations -- 12.4.4 Noise in the vibratory channel -- 12.5 Localization of the signal -- 12.6 The costs of acousticcommunication: 'unintended receivers' (see 'eavesdropping' in Chapter 10) -- 12.7 The receiver: insect ears -- 12.7.1 Evolution of ears in two behavioral contexts: intraspecific communication andpredator avoidance -- 12.7.2 Receptor organs for near-field and far-field sound and substrate vibrations -- Antennal ears for near-field sound -- Tympanal ears for far-field sound -- Vibration receptors -- 12.8 Conclusion -- Acknowledgements -- References -- CHAPTER 13: Reproductive behavior -- 13.1 Introduction to reproductive behavior -- 13.1.1 Basic anatomy and physiology -- 13.1.2 Parental investment -- 13.1.3 Sexual selection. , 13.1.4 Mating systems.
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Marine mammal science 14 (1998), S. 0 
    ISSN: 1748-7692
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A female hybrid between a fin (Balaenoptera physalus) and a blue whale (B. mnusculus) was caught in whaling operations in 1984 off northwestern Spain. Its coloration and body proportions were intermediate between those of a fin and a blue whale, although it was anomalously large (19.4 m) when compared to fin whales of similar age (4 yr). It was sexually immature, concomitant with its age but not its length if it were a fin whale. Molecular analyses revealed that the mother of the hybrid was a blue whale and the father a fin whale. Examination of data for the five fin-blue whale hybrids in the literature, plus other anecdotal reports, indicates that hybridization between these two species occurs in various geographic regions and is relatively frequent, notably in light of the absence of reported hybrids between other mysticetes. Either species may act as father or mother, and there does not appear to be a selection for a given sex among the hybrids. The reproductive capacity of these hybrids remains unknown, although incidence of reproductive impairment appears to be higher in hybrid males than in hybrid females.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Marine mammal science 3 (1987), S. 0 
    ISSN: 1748-7692
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Organochlorine pollutants are potentially useful for identifying discrete populations of marine mammals that overlap in geographic distribution. However, many factors unrelated to geographical distribution may affect the chemical burden of individual animals or of entire population components even within a homogeneously distributed population. These factors include. among others, nutritional state, sex, age, trophic level, distance of habitat from mainland and pollution source, excretion. metabolism, and tissue composition. Sample storage and analytical methodology may also be an important source of variation. These, and any other factors, must be identified and their effect ascertained before attempting any comparison between populations. This paper critically examines the nature and magnitude of the effects of these factors on organochlorine tissue loads in marine mammals. Pollutant concentrations can be strongly biased if carefully designed sampling regimes are not followed, but they are affected only moderately by sample treatment after collection. Conversely, ratios between concentrations of compounds, such as the DDE/tDDT or the tDDT/PCB ratios, seem less dependent on sampling regime but more affected by storage. analytical procedures and ecological variations such as distance from pollutant source or trophic level. Taking these effects into account, advice is provided about sampling and strategies for selection of variables that will improve the reliability of the comparisons between populations.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Marine mammal science 16 (2000), S. 0 
    ISSN: 1748-7692
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The use of photo-identification and its reliability in capture-recapture studies of Mediterranean monk seals were assessed using slides collected in the colony at Cap Blanc, western Sahara, from 1993 to 1996. Five tests indicated that researchers involved in photo-identification were proficient in matching slides of identified seals, consistent in classifying the side of the seal shown in slides and in assigning the morphological stage of the seal, and that changes of markings over a period of three years were insufficient to affect matching success. The certainty of identifying a seal was not dependent on the number of slides used but on distinctiveness of the markings and the quality of the slides taken. Capture-recapture abundance estimates were biased upwards when including poor quality slides. The exclusive use of excellent- and good quality slides provided the best estimates. The proportion of distinctive seals varied between morphological stages and was significantly lower in juveniles. When including the identification histories of juveniles, the heterogeneity of capture probabilities was higher. Therefore, abundance estimates were less biased when all juveniles were considered as non-distinctive seals. Reliable abundance estimates required a balance between duration of capture occasions and time interval between these.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1748-7692
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A survey was conducted in the summer of 1991 in the western Mediterranean to map the distribution and to estimate the number of striped dolphins surviving the 1990 outbreak of the morbillivirus epizootic. The highest densities of striped dolphins were found in the Alboran Sea and the Ligurian Sea. Total numbers were estimated at 117,880 (SE: 38,962; 95% CI: 68,379–214,800). The mortality resulting from the epizootic is unknown but may have been severe because the mean size of dolphin schools observed during the epizootic outbreak was significantly smaller than that before the event. A return to larger school sizes after the 1990 outbreak is not evidence of a recovery but can be viewed as a regrouping of individuals into schools of a preferred size. Calves were observed in 24.6% of the schools. They were not seen in schools of ten or less but were present in about half the schools of 30 or more dolphins, a result which suggests segregation similar to that seen in populations of this species elsewhere in the world.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Marine mammal science 15 (1999), S. 0 
    ISSN: 1748-7692
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Marine mammal science 5 (1989), S. 0 
    ISSN: 1748-7692
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Marine mammal science 10 (1994), S. 0 
    ISSN: 1748-7692
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: During the morbillivirus epizootic that affected the Mediterranean striped dolphins (Stenella coeruleoalba)in 1990–1992, several thous and individuals are believed to have died. In order to determine the segments of the population that were affected by the event, the sex- and age-frequency distributions of the animals that were washed ashore on the Spanish coasts were studied. The age of the animals was determined by counting dentine growth layer groups in the teeth. The results obtained indicate that both sexes were affected similarly by the disease and that the population component that suffered the largest mortality was that of sexually mature individuals, although substantial mortality of calves, probably still dependent on their mothers, was also observed. Juveniles, in contrast, appeared to be only slightly affected by the epizootic. This pattern of mortality is not consistent with the epidemiology of morbillivirus infections previously observed in other mammals. Possible explanations of this particular age distribution include behavioral factors, increased susceptibility to the disease in adults due to the effects of pollution, high temperatures and decreased food availability, or allopatric geographical distribution of population components and, therefore, of their associated mortality.
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