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By the best selling author of The Selfish Gene

People commonly view evolution as a process of competition between individuals--known as "survival of the fittest"--with the individual representing the "unit of selection." Richard Dawkins offers a controversial reinterpretation of that idea in The Extended Phenotype, now being reissued to coincide with the publication of the second edition of his highly-acclaimed The Selfish Gene. He proposes that we look at evolution as a battle between genes instead of between whole organisms. We can then view Nanges in phenotypes--the end products of genes, like eye color or leaf shape, which are usually considered to increase the fitness of an individual--as serving the evolutionary interests of genes. Dawkins makes a convincing case that considering one's body, personality, and environment as a field of combat in a kind of "arms race" between genes fighting to express themselves on a strand of DNA can clarify and extend the idea of survival of the fittest. This influential

People commonly view evolution as a process of competition between individuals--known as "survival of the fittest"--with the individual representing the "unit of selection." Richard Dawkins offers a controversial reinterpretation of that idea in The Extended Phenotype, now being reissued to coincide with the publication of the second edition of his highly-acclaimed The Selfish Gene. He proposes that we look at evolution as a battle between genes instead of between whole organisms. We can then view Nanges in phenotypes--the end products of genes, like eye color or leaf shape, which are usually considered to increase the fitness of an individual--as serving the evolutionary interests of genes. Dawkins makes a convincing case that considering one's body, personality, and environment as a field of combat in a kind of "arms race" between genes fighting to express themselves on a strand of DNA can clarify and extend the idea of survival of the fittest. This influential

People commonly view evolution as a process of competition between individuals--known as "survival of the fittest"--with the individual representing the "unit of selection." Richard Dawkins offers a controversial reinterpretation of that idea in The Extended Phenotype, now being reissued to coincide with the publication of the second edition of his highly-acclaimed The Selfish Gene. He proposes that we look at evolution as a battle between genes instead of between whole organisms. We can then view Nanges in phenotypes--the end products of genes, like eye color or leaf shape, which are usually considered to increase the fitness of an individual--as serving the evolutionary interests of genes. Dawkins makes a convincing case that considering one's body, personality, and environment as a field of combat in a kind of "arms race" between genes fighting to express themselves on a strand of DNA can clarify and extend the idea of survival of the fittest. This influential and controversial book illuminates the complex world of genetics in an engaging, lively manner.

A new voice in the nature-nurture debate can be heard at the interface between evolution and development. Phenotypic integration--or, how large numbers of characteristics are related to make up the whole organism, and how these relationships evolve and change their function--is a major growth area in research, attracting the attention of evolutionary biologists, developmental biologists, and geneticists, as well as, more broadly, ecologists, physiologists, and paleontologists. This edited collection presents much of the best and most recent work the topic.

A new voice in the nature-nurture debate can be heard at the interface between evolution and development. Phenotypic integration--or, how large numbers of characteristics are related to make up the whole organism, and how these relationships evolve and change their function--is a major growth area in research, attracting the attention of evolutionary biologists, developmental biologists, and geneticists, as well as, more broadly, ecologists, physiologists, and paleontologists. This edited collection presents much of the best and most recent work the topic.

"This is clearly the most authoritative and contemporary statement of current knowledge yet published." from the Foreword by H. Sarnat Tuberous sclerosis is the prototype of a category of malformations uniquely characterized by disturbances in cellular differentiation and growth. It presents with a complex association of different neurological phenotypes, including seizures, cognitive impairments and autism. It is important not only because it is a relatively common hereditary neurological disease with high morbidity, but because it has implications in other pathological processes, such as dysplasia and neoplasia, hamartoma formation and other disturbances in morphogenic processes. This book correlates new genetic data and basic science, covers clinical presentation, reviews the historical background and current diagnostic criteria, and deals with the recent advances in neuropathology, molecular genetics and neurobiology which give a better understanding of the pathogenesis of the disease. Paediatricians and child neurologists will find this book uniquely useful.

The first volume in the new Cambridge Handbooks in Behavioral Genetics series, Behavioral Genetics of the Mouse provides baseline information on normal behaviors, essential in both the design of experiments using genetically modified or pharmacologically treated animals and in the interpretation and analyses of the results obtained. The book offers a comprehensive overview of the genetics of naturally occurring variation in mouse behavior, from perception and spontaneous behaviors such as exploration, aggression, social interactions and motor behaviors, to reinforced behaviors such as the different types of learning. Also included are numerous examples of potential experimental problems, which will aid and guide researchers trying to troubleshoot their own studies. A lasting reference, the thorough and comprehensive reviews offer an easy entrance into the extensive literature in this field, and will prove invaluable to students and specialists alike.

This classic text covers over 700 different genetic syndromes affecting body structures, and has established itself as the definitive, comprehensive work on the subject. The discussion covers the phenotype spectrum, epidemiology, mode of inheritance, pathogenesis, and clinical profile of each condition, all of which is accompanied by a wealth of illustrations. The authors are recognized leaders in the field, and their vast knowledge and strong clinical judgment will help readers make sense of this complex and burgeoning field. New syndromes have been added to this edition and existing syndromes have been updated. This book will appeal to clinical geneticists, pediatricians, neurologists, head and neck surgeons, otolaryngologists, and dentists.

One aim of this atlas is to present a comprehensive overview of limb malformation phenotypes in order to provide the clinician with a tool that facilitates the diagnostic process. With the enormous advances in molecular and developmental biology, the genetic basis of many limb malformations and their relationship to each other has been elucidated. Thus, a further aim of this atlas is to provide the reader with a basic understanding of the molecular pathology of these conditions.The book is extensively illustrated with clinical photos and radiographs of conditions or groups of related conditions. In addition, a concise description of the conditions is provided featuring structured information on “Synonyms”, “Major clinical findings”, “Genetic transmission”, “Differential diagnosis”, “Molecular Pathology”, and references to Mendelian Inheritance in Man (OMIM).The book is designed for medical geneticists, radiologists, pediatricians, hand surgeons, orthopedic surgeons, as well as medical personnel and other physicians involved in the evaluation and treatment of patients with abnormal limbs.

 This book represents the results of 45 years of research on a wide range of topics, including atomic physics, single-molecule enzymology, whole-cell metabolism, physiology, pharmacology, linguistics, semiotics, and cosmology. It describes the first comprehensive molecular theory of the genotype-phenotype coupling based on two key theoretical concepts: (i) the conformon, the conformational wave packet in biopolymers carrying both the free energy and genetic information; and (ii) the intracellular dissipative structures, the chemical concentration waves inside the cell that serve as the immediate drivers of all cell functions. Conformons provide the driving forces for all molecular machines in the cell, and intracellular dissipative structures coordinate intra- and intercellular processes such as gene expression and cell-cell communications.One of the predictions made by the cell language theory (CLT) is that there are two forms of genetic information — the Watson–Crick genes transmitting information in time (identified with DNA), and the Prigoginian genes transmitting information in space (identified with RNA expression profiles). The former is analogous to sheet music or written language and the latter is akin to audio music or spoken language, both being coupled by conformons acting as the analog of the pianist. The new theory of DNA structure and function constructed on the basis of CLT can rationally account for most of the puzzling findings recently unearthed by the ENCODE (Encyclopedia of DNA Elements) project.The Cell Language Theory has important applications in biomedical sciences including drug discovery research and personalized medicine on the one hand and in the mind-body research and consciousness studies on the other.

The lastest edition of this classic text continues to provide the basis for understanding the genetic principles behind quantitative differences in phenotypes and how they apply to animal and plant improvement and evolution. It extends these concepts to the segregation of genes that cause genetic variation in quantitative traits. Key techniques and methods are also covered.

Crustaceans are increasingly being used as model organisms in all fields of biology, including neurobiology, developmental biology, animal physiology, evolutionary ecology, biogeography, and resource management. Crustaceans have a very wide range of phenotypes and inhabit a diverse array of environments, ranging from the deep sea to high mountain lakes and even deserts. The evolution of their life histories has permitted crustaceans to successfully colonize this variety of habitats. Few other taxa exhibit such a variety of life histories and behavior. A comprehensive overview of their life histories is essential to the understanding of many aspects of their success in marine and terrestrial environments. This volume provides a general overview of crustacean life histories. Crustaceans have particular life history adaptations that have permitted them to conquer all environments on earth. Crustacean life cycles have evolved to maximize fecundity, growth, and ageing, in a wide range of environmental conditions. Individual contributions contrast benefits and costs of different life histories including sexual versus asexual production, semelparity versus iteroparity, and planktonic larvae versus direct development. Important aspects of particular behaviors are presented (e.g. migrations, defense and territorial behaviors, anti-predator behavior, symbiosis).

 This book represents the results of 45 years of research on a wide range of topics, including atomic physics, single-molecule enzymology, whole-cell metabolism, physiology, pharmacology, linguistics, semiotics, and cosmology. It describes the first comprehensive molecular theory of the genotype-phenotype coupling based on two key theoretical concepts: (i) the conformon, the conformational wave packet in biopolymers carrying both the free energy and genetic information; and (ii) the intracellular dissipative structures, the chemical concentration waves inside the cell that serve as the immediate drivers of all cell functions. Conformons provide the driving forces for all molecular machines in the cell, and intracellular dissipative structures coordinate intra- and intercellular processes such as gene expression and cell-cell communications.One of the predictions made by the cell language theory (CLT) is that there are two forms of genetic information — the Watson–Crick genes transmitting information in time (identified with DNA), and the Prigoginian genes transmitting information in space (identified with RNA expression profiles). The former is analogous to sheet music or written language and the latter is akin to audio music or spoken language, both being coupled by conformons acting as the analog of the pianist. The new theory of DNA structure and function constructed on the basis of CLT can rationally account for most of the puzzling findings recently unearthed by the ENCODE (Encyclopedia of DNA Elements) project.The Cell Language Theory has important applications in biomedical sciences including drug discovery research and personalized medicine on the one hand and in the mind-body research and consciousness studies on the other.

This classic text covers over 700 different genetic syndromes affecting body structures, and has established itself as the definitive, comprehensive work on the subject. The discussion covers the phenotype spectrum, epidemiology, mode of inheritance, pathogenesis, and clinical profile of each condition, all of which is accompanied by a wealth of illustrations. The authors are recognized leaders in the field, and their vast knowledge and strong clinical judgment will help readers make sense of this complex and burgeoning field. New syndromes have been added to this edition and existing syndromes have been updated. This book will appeal to clinical geneticists, pediatricians, neurologists, head and neck surgeons, otolaryngologists, and dentists.

What does it mean to "act black" or "act white"? Is race merely a matter of phenotype, or does it come from the inflection of a person's speech, the clothes in her closet, how she chooses to spend her time and with whom she chooses to spend it? What does it mean to be "really" black, and who gets to make that judgment?In Acting White?, leading scholars of race and the law Devon Carbado and Mitu Gulati argue that, in spite of decades of racial progress and the pervasiveness of multicultural rhetoric, racial judgments are often based not just on skin color, but on how a person conforms to behavior stereotypically associated with a certain race. Specifically, racial minorities are judged on how they "perform" their race. This performance pervades every aspect of their daily life, whether it's the clothes they wear, the way they style their hair, the institutions with which they affiliate, their racial politics, the people they befriend, date or marry, where they live, how they speak, and their outward mannerisms and demeanor. Employing these cues, decision-makers decide not simply whether a person is black but the degree to which she or he is so. Relying on numerous examples from the workplace, higher education, and police interactions, the authors demonstrate that, for African Americans, the costs of "acting black" are high, and so are the pressures to "act white." But, as the authors point out, "acting white" has costs as well. Provocative yet never doctrinaire, Acting White? will boldly challenge your assumptions and make you think about racial prejudice from a fresh vantage point.

Evolutionary maternal effects occur whenever a mother’s phenotypic traits directly affect her offspring’s phenotype, independent of the offspring’s genotype. Some of the phenotypic traits that result in maternal effects have a genetic basis, whereas others are environmentally determined. For example, the size of a litter produced by a mammalian mother—a trait with a strong genetic basis—can affect the growth rate of her offspring, while a mother’s dominance rank—an environmentally determined trait—can affect the dominance rank of her offspring. The first volume published on the subject in more than a decade, Maternal Effects in Mammals reflects advances in genomic, ecological, and behavioral research, as well new understandings of the evolutionary interplay between mothers and their offspring. Dario Maestripieri and Jill M. Mateo bring together a learned group of contributors to synthesize the vast literature on a range of species, highlight evolutionary processes that were previously overlooked, and propose new avenues of research. Maternal Effects in Mammals will serve as the most comprehensive compendium on and stimulus for interdisciplinary treatments of mammalian maternal effects.

The lastest edition of this classic text continues to provide the basis for understanding the genetic principles behind quantitative differences in phenotypes and how they apply to animal and plant improvement and evolution. It extends these concepts to the segregation of genes that cause genetic variation in quantitative traits. Key techniques and methods are also covered.

Professor Parsons uses the colonizing species as a case study in the dynamics of microevolution at work in living systems. The colonizing species, a lie, and potentially disruptive force in a 'naïve' habitat, is studied primarily as an ecological phenotype and more generally as an ecological behavioural phenotype. Conventional life-history traits and components of fitness, can be incorporated into these phenotypes. Integrating genetic change, natural selection, and the interaction of the species with its environment and other living systems therein, the colonizing species is transformed into a sophisticated and complex source of data for understanding evolutionary biology. Throughout the book it is emphasized that using the organism as the unit of selection is the most direct way of understanding the nature of successful colonizing phenotypes, and, by using specific phenotypic criteria, the prediction of likely successful colonists can be made. Such criteria include tolerance of extreme environments, resource utilization, reproductive capacity, and relative abundance.

Genome sequences are now available that enable us to determine the biological components that make up a cell or an organism. The new discipline of systems biology examines how these components interact and form networks, and how the networks generate whole cell functions corresponding to observable phenotypes. This textbook describes how to model networks, determine their properties, and relate these to phenotypic functions. Some knowledge of linear algebra and biochemistry is required, since the book reflects the irreversible trend of increasing mathematical content in biology education.