Spatial Patterns Of Genetic Variation
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| Author | : Bryan K. Epperson |
| Publisher | : Princeton University Press |
| Total Pages | : 376 |
| Release | : 2003-08-11 |
| Genre | : Science |
| ISBN | : 1400835623 |
Population genetics has made great strides in applying statistical analysis and mathematical modeling to understand how genes mutate and spread through populations over time. But real populations also live in space. Streams, mountains, and other geographic features often divide populations, limit migration, or otherwise influence gene flow. This book rigorously examines the processes that determine geographic patterns of genetic variation, providing a comprehensive guide to their study and interpretation. Geographical Genetics has a unique focus on the mathematical relationships of spatial statistical measures of patterns to stochastic processes. It also develops the probability and distribution theory of various spatial statistics for analysis of population genetic data, detailing exact methods for using various spatial features to make precise inferences about migration, natural selection, and other dynamic forces. The book also reviews the experimental literature on the types of spatial patterns of genetic variation found within and among populations. And it makes an unprecedented strong connection between observed measures of spatial patterns and those predicted theoretically. Along the way, it introduces readers to the mathematics of spatial statistics, applications to specific population genetic systems, and the relationship between the mathematics of space-time processes and the formal theory of geographical genetics. Written by a leading authority, this is the first comprehensive treatment of geographical genetics. It is a much-needed guide to the theory, techniques, and applications of a field that will play an increasingly important role in population biology and ecology.
| Author | : W.T. Adams |
| Publisher | : Springer Science & Business Media |
| Total Pages | : 442 |
| Release | : 1992-11-30 |
| Genre | : Science |
| ISBN | : 9780792318576 |
Tropical climates, which occur between 23°30'N and S latitude (Jacob 1988), encompass a wide variety of plant communities (Hartshorn 1983, 1988), many of which are diverse in their woody floras. Within this geographic region, temperature and the amount and seasonality of rainfall define habitat types (UNESCO 1978). The F AO has estimated that there 1 are about 19 million km of potentially forested area in the global tropics, of which 58% were estimated to still be in closed forest in the mid-1970s (Sommers 1976; UNESCO 1978). Of this potentially forested region, 42% is categorized as dry forest lifezone, 33% is tropical moist forest, and 25% is wet or rain forest (Lugo 1988). The species diversity of these tropical habitats is very high. Raven (1976, in Mooney 1988) estimated that 65% of the 250,000 or more plant species of the earth are found in tropical regions. Of this floristic assemblage, a large fraction are woody species. In the well-collected tropical moist forest of Barro Colorado Island, Panama, 39. 7% (481 of 1212 species) of the native phanerogams are woody, arborescent species (Croat 1978). Another 21. 9% are woody vines and lianas. Southeast Asian Dipterocarp forests may contain 120-200 species of trees per hectare (Whitmore 1984), and recent surveys in upper Amazonia re corded from 89 to 283 woody species ~ 10 cm dbh per hectare (Gentry 1988). Tropical communities thus represent a global woody flora of significant scope.
| Author | : National Research Council |
| Publisher | : National Academies Press |
| Total Pages | : 101 |
| Release | : 1998-01-19 |
| Genre | : Science |
| ISBN | : 0309184746 |
This book assesses the scientific value and merit of research on human genetic differencesâ€"including a collection of DNA samples that represents the whole of human genetic diversityâ€"and the ethical, organizational, and policy issues surrounding such research. Evaluating Human Genetic Diversity discusses the potential uses of such collection, such as providing insight into human evolution and origins and serving as a springboard for important medical research. It also addresses issues of confidentiality and individual privacy for participants in genetic diversity research studies.
| Author | : National Academy of Sciences |
| Publisher | : |
| Total Pages | : 388 |
| Release | : 2007 |
| Genre | : Science |
| ISBN | : |
The Arthur M. Sackler Colloquia of the National Academy of Sciences address scientific topics of broad and current interest, cutting across the boundaries of traditional disciplines. Each year, four or five such colloquia are scheduled, typically two days in length and international in scope. Colloquia are organized by a member of the Academy, often with the assistance of an organizing committee, and feature presentations by leading scientists in the field and discussions with a hundred or more researchers with an interest in the topic. Colloquia presentations are recorded and posted on the National Academy of Sciences Sackler colloquia website and published on CD-ROM. These Colloquia are made possible by a generous gift from Mrs. Jill Sackler, in memory of her husband, Arthur M. Sackler.
| Author | : Tong H. Joh |
| Publisher | : |
| Total Pages | : 188 |
| Release | : 1990 |
| Genre | : Medical |
| ISBN | : |
The study of the genomic regulation of catecholamine-related enzymes is a new field, emerging from the rapid advances in molecular neurobiology. This text offers detailed summaries of recent progress from the work of leading researchers in molecular genetics and enzymes. It concentrates primarily on the rate- limiting enzyme tyrosine hydroxylase, with several chapters devoted to its complex chemistry, plus an evolutionary view of its structural similarity to certain aromatic amino acid hydroxylases. The book covers the remaining three pathway enzymes and all other enzymes related to catecholamine genes.
| Author | : Richard Frankham |
| Publisher | : Oxford University Press |
| Total Pages | : 426 |
| Release | : 2017 |
| Genre | : Biodiversity |
| ISBN | : 0198783396 |
One of the greatest unmet challenges in conservation biology is the genetic management of fragmented populations of threatened animal and plant species. More than a million small, isolated, population fragments of threatened species are likely suffering inbreeding depression and loss of evolutionary potential, resulting in elevated extinction risks. Although these effects can often be reversed by re-establishing gene flow between population fragments, managers very rarely do this. On the contrary, genetic methods are used mainly to document genetic differentiation among populations, with most studies concluding that genetically differentiated populations should be managed separately, thereby isolating them yet further and dooming many to eventual extinction Many small population fragments are going extinct principally for genetic reasons. Although the rapidly advancing field of molecular genetics is continually providing new tools to measure the extent of population fragmentation and its genetic consequences, adequate guidance on how to use these data for effective conservation is still lacking. This accessible, authoritative text is aimed at senior undergraduate and graduate students interested in conservation biology, conservation genetics, and wildlife management. It will also be of particular relevance to conservation practitioners and natural resource managers, as well as a broader academic audience of conservation biologists and evolutionary ecologists.
| Author | : Ernst Bauernfeind |
| Publisher | : BRILL |
| Total Pages | : 779 |
| Release | : 2013-01-21 |
| Genre | : Science |
| ISBN | : 9004260889 |
Among the various groups of aquatic insects, mayflies (Ephemeroptera) are of special interest for professional limnologists and entomological researchers as well as for naturalists in general and even the dedicated fly angler. Identification has traditionally been considered difficult and implementation in environmental monitoring and freshwater management has led to an ever increasing demand for exact information on taxonomy and ecology. The present handbook is designed to provide for the first time an up-to-date standard work for Ephemeroptera identification, including last instar larvae (nymphs), subimago (dun), male and female imagines. Recent changes in nomenclature are discussed in detail as well as gaps in current knowledge and probable pitfalls concerning the reliable identification of all taxa known so far from the region. Keys are provided for genera and introductory chapters characterize every family and genus. Species accounts follow a common format providing a synonymy, characters for identification (including literature references), remarks (on type material, variation, confusing or extralimital species) and short information on biology and distribution pattern. Male genitalia are illustrated by micrographs and line drawings, REM photographs of the egg chorionic structure are provided for genera and selected species. Habitus of larvae and imagines are for most genera illustrated by colour photographs. The geographical area covered is Europe including the European part of Russia, the mediterranean islands and North Africa. Short additional information is provided for adjacent parts of the western Palaearctic Region. A comprehensive index, check-list and distribution catalogue (following the widely adopted concept of Illies’ Limnofauna Europaean) allow for quick information on all species recorded so far from Europe.
| Author | : Barbara Landau |
| Publisher | : Oxford University Press |
| Total Pages | : |
| Release | : 2012-08-23 |
| Genre | : Psychology |
| ISBN | : 0199921377 |
Our experience of the spatial world is a unitary one; we perceive objects and layouts, we remember them and act on them, and we can even talk about them with ease. Despite this impression of seamlessness, spatial representations in human adults appear to be specialized in domain-dependent manner, engaging different properties and computational mechanisms for different functions. In this book, the authors present evidence that this domain-specific specialization in cognitive function emerges early in development and is reflected in patterns of breakdown that occur under genetic defect. The authors focus on spatial representation in children and adults with Williams syndrome, a relatively rare genetic syndrome that gives rise to an unusual profile of severely impaired spatial representation together with spared language. Results from a variety of spatial domains -- including object representation, motion perception, action, navigation, and spatial language -- appear to display a strikingly uneven profile of sparing and deficit within spatial representations, consistent with the idea that specialization of function drives development and breakdown. These findings raise a crucial question: Can specific genes target specific aspects of cognitive structure? Looking deeper into the patterns of performance across spatial domains, the book explores the notion that understanding patterns of normal development across domains is crucial to understanding unusual development. Using insights from normal development, the authors propose a speculative hypothesis that explains the emergence of the William syndrome profile, and how complex cognitive outcomes can arise from the deletion of a small set of genes.
| Author | : L L Cavalli-sforza |
| Publisher | : Princeton University Press |
| Total Pages | : 430 |
| Release | : 2018-06-05 |
| Genre | : Science |
| ISBN | : 0691187266 |
Hailed as a breakthrough in the understanding of human evolution, The History and Geography of Human Genes offers the first full-scale reconstruction of where human populations originated and the paths by which they spread throughout the world. By mapping the worldwide geographic distribution of genes for over 110 traits in over 1800 primarily aboriginal populations, the authors charted migrations and devised a clock by which to date evolutionary history. This monumental work is now available in a more affordable paperback edition without the myriad illustrations and maps, but containing the full text and partial appendices of the authors' pathbreaking endeavor.
| Author | : Joel T. Dudley |
| Publisher | : Oxford University Press |
| Total Pages | : 265 |
| Release | : 2013-01-03 |
| Genre | : Medical |
| ISBN | : 0199644489 |
Rapid advances in high-throughput genome sequencing technologies foreshadow a near-future in which millions of individuals will gain affordable access to their complete genome sequence. This promises to give unprecedented insights into the fundamental biological nature of ourselves and our species: where we came from, how we are born, how we interact with our environment, how we get sick, how we get well, and how we age. Personal genomics is therefore an important component of the inevitable transition towards personalized medicine, as the medical establishment begins to explore and evaluate the role of personal genomics in health and medicine. However there is currently very little training available for medical practitioners. Exploring Personal Genomics provides a novel, inquiry-based approach to understanding and interpreting the practical, medical, and societal aspects of personal genomic information. It is presented in two parts: the first provides readers of all backgrounds with a fundamental understanding of the biology of human genomes, information on how to obtain and understand digital representations of personal genomic data, tools and techniques for exploring the personal genomics of ancestry and genealogy, discovery and interpretation of genetic trait associations, and the role of personal genomics in drug response. The second part offers more advanced readers an understanding of the science, tools, and techniques for investigating interactions between a personal genome and the environment, connecting DNA to physiology, assessing rare variants and structural variation, and exploring resources for performing personal biological investigation. This advanced textbook is primarily aimed at undergraduate and graduate students taking classes in genomic medicine, genetics, and bioinformatics. It will also be of relevance and use to medical practitioners, evolutionary biologists, geneticists and individuals interested in exploring their personal genetic data.
