基于生物适应进化原理论证生物进化的动力

文章从现有主流生物进化理论存在的问题入手, 以生物适应进化原理为认识基础, 讨论生物进化的动力, 以求对生物进化机制有一个新的认识。在薛定谔“生命赖负熵生存”观点的指导下, 提出了“负熵流”包括能量流、物质流和信息流, 以及负熵流是生命生存和发育的动力的观点。作者在原有生物适应进化原理基础上, 修改完善并提出了“DNA、RNA和蛋白质在环境作用下的生物适应进化调控系统”理论, 并根据系统发育是个体发育的“积分”的观点, 推论得出生物与环境的负熵差引起的负熵流也是生命进化的动力, 对生物进化机制作出了新的理解。基于这样的生物进化机制的认识, 提出了“进化是一个子系统在其上一等级系统中, 将自身全部或部分信息遗传给下一代子系统, 并在其适应上一等级系统过程中, 产生一些新质, 终止一些旧质, 从而在其上一等级系统中得以延续的变化过程”的概念, 并探讨了一些与进化有关的其他争议问题。     

Natural Selection: A Misnomer Concept

Charles Robert Darwin hypothesized that the mechanism of evolution and the diversity of life on earth are because of natural selection. That is, which biological entity would thrive on earth is a matter of selection by the nature. But, in the present article it is hypothesized that the process of appearance of different types of biological entities and the orientation of these organisms in the space in respect to time are the effects of ‘will force’ of the organisms concerned. That is, the mechanism of evolution is a process of self selection, not natural selection.     

The logic of asymmetric contests

A theoretical analysis is made of the evolution of behavioural strategies in contest situations. It is assumed that behaviour will evolve so as to maximize individual fitness. If so, a population will evolve an ‘evolutionarily stable strategy’, or ESS, which can be defined as a strategy such that, if all members of a population adopt it, no ‘mutant’ strategy can do better. A number of simple models of contest situations are analysed from this point of view. It is concluded that in ‘symmetric’ contests the ESS is likely to be a ‘mixed’ strategy; that is, either the population will be genetically polymorphic or individuals will be behaviourally variable. Most real contests are probably asymmetric, either in pay-off to the contestants, or in size or weapons, or in some ‘uncorrelated’ fashion; i.e. in a fashion which does not substantially bias either the pay-offs or the likely outcome of an escalated contest. An example of an uncorrelated asymmetry is that between the ‘discoverer’ of a resource and a ‘late-comer’. It is shown that the ESS in asymmetric contests will usually be to permit the asymmetric cue to settle the contest without escalation. Escalated contests will, however, occur if information to the contestants about the asymmetry is imperfect.     

Vitalism and the Resistance to Experimentation on Life in the Eighteenth Century

There is a familiar opposition between a ‘Scientific Revolution’ ethos and practice of experimentation, including experimentation on life, and a ‘vitalist’ reaction to this outlook. The former is often allied with different forms of mechanism – if all of Nature obeys mechanical laws, including living bodies, ‘iatromechanism’ should encounter no obstructions in investigating the particularities of animal-machines – or with more chimiatric theories of life and matter, as in the ‘Oxford Physiologists’. The latter reaction also comes in different, perhaps irreducibly heterogeneous forms, ranging from metaphysical and ethical objections to the destruction of life, as in Margaret Cavendish, to more epistemological objections against the usage of instruments, the ‘anatomical’ outlook and experimentation, e.g. in Locke and Sydenham. But I will mainly focus on a third anti-interventionist argument, which I call ‘vitalist’ since it is often articulated in the writings of the so-called Montpellier Vitalists, including their medical articles for the Encyclopédie. The vitalist argument against experimentation on life is subtly different from the metaphysical, ethical and epistemological arguments, although at times it may borrow from any of them. It expresses a Hippocratic sensibility – understood as an artifact of early modernity, not as some atemporal trait of medical thought – in which Life resists the experimenter, or conversely, for the experimenter to grasp something about Life, it will have to be without torturing or radically intervening in it. I suggest that this view does not have to imply that Nature is something mysterious or sacred; nor does the vitalist have to attack experimentation on life in the name of some ‘vital force’ – which makes it less surprising to find a vivisectionist like Claude Bernard sounding so close to the vitalists.     

Lineages,splits and divergence challenge whether the terms anagenesis and cladogenesis are necessary

Using the framework of evolutionary lineages to separate the process of evolution and classification of species, we observe that ‘anagenesis’ and ‘cladogenesis’ are unnecessary terms. The terms have changed significantly in meaning over time, and current usage is inconsistent and vague across many different disciplines. The most popular definition of cladogenesis is the splitting of evolutionary lineages (cessation of gene flow), whereas anagenesis is evolutionary change between splits. Cladogenesis (and lineage‐splitting) is also regularly made synonymous with speciation. This definition is misleading as lineage‐splitting is prolific during evolution and because palaeontological studies provide no direct estimate of gene flow. The terms also fail to incorporate speciation without being arbitrary or relative, and the focus upon lineage‐splitting ignores the importance of divergence, hybridization, extinction and informative value (i.e. what is helpful to describe as a taxon) for species classification. We conclude and demonstrate that evolution and species diversity can be considered with greater clarity using simpler, more transparent terms than anagenesis and cladogenesis. Describing evolution and taxonomic classification can be straightforward, and there is no need to ‘make words mean so many different things’.     

Living in a Clinic: The Power of Public Health Promotions

Drawing on an anthropological study of the Cessnock area of New South Wales, this paper considers the politics of recent health promotion campaigns in Australia, placing the new ‘healthist’ discourse in its historical context. Whereas Cessnock people were once said to be bestial, or childish, or sick, they are now said to be fat. Whereas Methodism was once prescribed as the solution, doctors now order a rational and maximising attitude to life. It is argued that the undoubted seriousness of Cessnock's health ‘problem’ and the undoubted good will of the health promoters do not remove the danger of cultural imperialism.     

Evolution Versus Creationism: A matter of acceptance versus belief

Scientists are often challenged about their ‘belief’ in evolution. Many creationists try to convince people that evolution is more of a ‘faith-based’ position or belief system than ‘real science’. This article examines the notion of acceptance versus belief and the relationship between knowledge, understanding and belief. It argues that adopting the acceptance of evolution over belief in evolution will help teachers deal with the challenges that inevitably arise in lessons on evolution in high school. Studies in philosophy show beliefs are often held without evidence, may be illogical and are difficult to change. Acceptance of a scientific explanation for a natural phenomenon, however, is based on evidence and allows for a change in disposition should new evidence come to light. With this in mind, removing the idea of ‘belief’ in evolution and talking about acceptance provides a sensible way to manage talk of creationism versus evolution, if and when it arises in the classroom.     

Carbon sequestration in tropical forests and water: a critical look at the basis for commonly used generalizations

Tree planting in the tropics is conducted for a number of reasons including carbon sequestration, but often competes with increasingly scarce water resources. The basics of forest and water relations are frequently said to be well understood but there is a pressing need to better understand and predict the hydrological effects of land‐use and climate change in the complex and dynamic landscapes of the tropics. This will remain elusive without the empirical data required to feed hydrological process models. It is argued that the current state of knowledge is confused by too broad a use of the terms ‘forest’ and ‘(af)forestation’, as well as by a bias towards using data generated mostly outside the tropics and for nondegraded soil conditions. Definitions of forest, afforestation and reforestation as used in the climate change community and their application by land and water managers need to be reconciled.     

Recent northward range expansion promotes song evolution in a passerine bird,the Light‐vented Bulbul

In common with human speech, song is culturally inherited in oscine passerine birds (‘songbirds’). Intraspecific divergence in birdsong, such as development of local dialects, might be an important early step in the speciation process. It is therefore vital to understand how songs diverge, especially in founding populations. The northward expansion of the Light‐vented Bulbul Pycnonotus sinensis (J. F. Gmelin, 1789) into north China in the last 30 years provides an excellent opportunity to study birdsong evolution. We compared ~4400 songs from newly established northern populations with ~2900 songs from southern populations to evaluate song divergence after recent expansion. The total pool of syllables and especially song types was considerably smaller in the north than in the south, indicating ‘founder effects’ in the new population. The ancestral pattern of mosaic song dialects changed into a pattern of wide geographical sharing of a few song types and syllables, likely the result of fewer geographical barriers to ‘meme flow’, and the recent spread across a large area in the north. Our results suggest that song evolution and vocal trait shifts can arise rapidly after range expansion, and that in the Light‐vented Bulbul ‘founder effects’, geographical isolation, and recent rapid expansions played important roles in the evolution of song dialects.     

Charles Darwin,embryology, evolution and skeletal plasticity

Darwin provided us with the theory of evolutionary change through natural selection. Just as important to the science of biology was Darwin’s recognition that all organisms could be classified and were related to one another because they arose from a single common universal ancestor – what we know as the universal tree of life (UtoL). All the features of the skeletal biology of fish therefore can be explained, both in an evolutionary framework (ultimate causation) and in the framework of development, growth and physiology (proximate causation). Neither approach is complete without the other. I will outline the elements of Darwin’s theories on evolution and classification and, as importantly, discuss what was missing from Darwin’s theories. An important class of evidence for evolution used by Darwin came from embryology, both comparative embryology and the existence of vestiges and atavisms. After discussing this evidence I examine some fundamental features of skeletal development and evolution These include: the presence of four skeletal systems in all vertebrates; the existence of two skeletons, one based on cartilage, the other on bone and dentine; the modular nature of skeletal development and evolution; and the plasticity of the skeleton in response to either genetic or environmental changes.     

Explanations in evolutionary theory1

The theory of biological evolution is defined in many ways, leading to considerable confusion in its application and testing against objective empirical observations. Evolutionary change is usually defined as genetic which would exclude both cultural and template evolution; hence the qualifying adjective genetic should not be included in the definition of biological evolution. Darwin's theory, always described by him in the singular, is actually a bundle of five independent theories about evolution as advocated by Mayr. Furthermore only one of these theories, that of common descent, is historical, and the other four – evolution as such, gradualism, processes of phyletic evolution and of speciation, and causes of evolution – are nomological. Hence not all evolutionary theory is historical. Biological comparisons can be divided into horizontal and vertical ones and valid conclusions from one type of comparisons cannot be automatically extrapolated to the other. All phyletic evolutionary change, no matter how extensive it may be, never crosses species taxa boundaries; hence it is not possible to distinguish ‘trans‐specific evolution’ (= evolution beyond or above the level of the species) from evolution within the species level. Macroevolution does not differ from microevolution except in the scale of the overall change; no special causes or processes of macroevolution exist.     

Virulence evolution and the trade‐off hypothesis: history,current state of affairs and the future

It has been more than two decades since the formulation of the so‐called ‘trade‐off’ hypothesis as an alternative to the then commonly accepted idea that parasites should always evolve towards avirulence (the ‘avirulence hypothesis’). The trade‐off hypothesis states that virulence is an unavoidable consequence of parasite transmission; however, since the 1990s, this hypothesis has been increasingly challenged. We discuss the history of the study of virulence evolution and the development of theories towards the trade‐off hypothesis in order to illustrate the context of the debate. We investigate the arguments raised against the trade‐off hypothesis and argue that trade‐offs exist, but may not be of the simple form that is usually assumed, involving other mechanisms (and life‐history traits) than those originally considered. Many processes such as pathogen adaptation to within‐host competition, interactions with the immune system and shifting transmission routes, will all be interrelated making sweeping evolutionary predictions harder to obtain. We argue that this is the heart of the current debate in the field and while species‐specific models may be better predictive tools, the trade‐off hypothesis and its basic extensions are necessary to assess the qualitative impacts of virulence management strategies.     

MORPHOLOGY OF THE CURD OF CAULIFLOWER

Sadik , Sidki . (U. California, Davis.) Morphology of the curd of cauliflower. Amer. Jour. Bot. 49(3): 290–297. Illus. 1962.—The development of the curd and inflorescence of cauliflower, Brassica oleracea Linn., var. botrytis D.C., is described. The cultivars ‘Snowball M’ and ‘February-Early-March’ were studied. The curd has a nonfasciated and monopodial type of branching. Curd initiation of ‘Snowball M’ is not dependent on vernalization, but the curd of ‘February-Early-March’ and the floral primordia of both cultivars are initiated only after vernalization. Associated with flowering is the disruption of the curd by the elongation of some of the inflorescence branches. The initiation of leaves, branches, and floral primordia follows a 5 + 8 phyllotaxy throughout all stages of development. This system of phyllotaxy changes at the time of initiation of floral parts.     

On the reconceptualization of Alzheimer’s disease

In the hope of future treatments to prevent or slow down the disease, there is a strong movement towards an ever‐earlier detection of Alzheimer’s disease (AD). In conjunction with scientific developments, this has prompted a reconceptualization of AD, as a slowly progressive pathological process with a long asymptomatic phase. New concepts such as ‘preclinical’ and ‘prodromal’ AD have been introduced, raising a number of conceptual and ethical questions. We evaluate whether these new concepts are theoretically defensible, in light of theories of health and disease, and whether they should be understood as disease or as an at‐risk state. We introduce a pragmatic view on disease concepts and argue that an evaluation of the reconceptualization of AD should also take its aims and effects into account, and assess their ethical acceptability. The reconceptualization of AD is useful to coordinate research into preventive strategies, and may potentially benefit future patients. However, in the short term, early detection and labelling of ‘preclinical AD’ can potentially harm people. Since there is no treatment available and the predictive value is unclear, it may only create a group of ‘patients‐in‐waiting’ who may suffer from anxiety, uncertainty and stigmatization, but will never actually develop dementia. We conclude that only if the promise of preventive medication materializes, will the reconceptualization of AD turn out unequivocally to be for the better. Otherwise, the reconceptualization may do more harm than good.     

A multigenerational effect of parental age on offspring size but not fitness in common duckweed (Lemna minor)

Classic theories on the evolution of senescence make the simplifying assumption that all offspring are of equal quality, so that demographic senescence only manifests through declining rates of survival or fecundity. However, there is now evidence that, in addition to declining rates of survival and fecundity, many organisms are subject to age‐related declines in the quality of offspring produced (i.e. parental age effects). Recent modelling approaches allow for the incorporation of parental age effects into classic demographic analyses, assuming that such effects are limited to a single generation. Does this ‘single‐generation’ assumption hold? To find out, we conducted a laboratory study with the aquatic plant Lemna minor, a species for which parental age effects have been demonstrated previously. We compared the size and fitness of 423 laboratory‐cultured plants (asexually derived ramets) representing various birth orders, and ancestral ‘birth‐order genealogies’. We found that offspring size and fitness both declined with increasing ‘immediate’ birth order (i.e. birth order with respect to the immediate parent), but only offspring size was affected by ancestral birth order. Thus, the assumption that parental age effects on offspring fitness are limited to a single generation does in fact hold for L. minor. This result will guide theorists aiming to refine and generalize modelling approaches that incorporate parental age effects into evolutionary theory on senescence.     

Animal signals: Ethological and games-theory approaches are not incompatible

Recent authors have contrasted the ‘traditional ethological approach’ to the study of animal signals with that derived from games theory. It is argued here that the ‘traditonal ethological approach’ they portray is not in keeping with main stream of ethological research on animal signals. In particular, it has not been generally assumed that the evolution of animal signals was based on selection for mutual benefit of actor and reactor, nor that signals carry precise information of what the actor will do next. A synthesis of the ethological and games-theory approaches is possible. It is suggested that many threat displays may signal ‘Will stay, but attack if provoked’ or ‘Will stay, but will flee if provoked’, and that the subsequent behaviour of the displaying bird depends in part on that of the reactor.     

Optimierung und ökonomisierung im kontext von evolutionstheorie und phylogenetischer rekonstruktion

The meaning of optimality and economy in phylogenetics and evolutionary biology is discussed. It can be shown that the prevailing concepts of optimality and economy are equivocal as they are not based on strict theoretical positions and as they have a variable meaning in different theoretical contexts. The ideas of optimality and economy can be considered to be identical with the expectation of a relatively simple order in a particular field of study. Although there exists no way of inferring one or several methods of solving scientific problems from the presupposed idea of economy and optimality, a lack of motivation for scientific investigations would result if the concepts of economy and optimality in nature were dropped. By reference to several examples, it is shown that the concepts of optimality and economy are only useful against the background of indispensable theories. If there is a shift from one theory to another, a restriction on the use of these concepts is necessary. Optimality and economy in the sense of operations research in engineering or economical sciences depend on the principle of minimum costs. Both theoretical concepts: technical efficiency in relation to the energy required to run a machine and profit maximation in an economical framework must be shown to be realistic assumptions. In the field of biology processes of optimization and economization are normally discussed under two different views:

1. The concept of economy is used in cases of functional adaptation when the organism makes good use of the building material which is available to fulfill one (or more) functions. The theoretical background must be seen in the energy-consuming aspect of the organism.
2. In evolutionary change and phylogeny ‘economization’ and ‘optimization’ are deduced from the evolutionary theory, and evolution is shown to produce a special kind of biological economy in biological systems (Bock & von Wahlert, 1965). The ‘Okonomie-Prinzip’ or ‘Lesrichtungskriterium’ points out the arguments needed to state a phylogenetic theory and to construct a dendrogram (Peters & Gutmann, 1971).

In every phylogenetic theory concerning the adaptational change in the evolving biological system an explanation for the function of all stages is required. Only those statements should be accepted as phylogenetic theories which are characterized by the demonstration of the process of economization in the functional relations of the evolving organism. The process of adaptation can be determined by the improved chance of some mutants to propagate their genetical information. In this process all functional systems in their interrelations — i.a. mutual dependence — and their relation with the environment add their functional efficiency to the information to be delivered to their progeny, because the more economical biological system in a certain environment will have a better chance to produce offspring. This outcome is affirmed by natural selection which works on all levels of the evolving biological systems (Gutmann & Peters 1973). Nevertheless a judgment about adaptation cannot be taken as a scale of measurement in the phylogenetic process. The conditions in the organism itself and in the environment or in the organic system alone can change in so profound a manner that the marginal conditions of the earlier stages of the process of adaptation are not the same as in the derived ones. During phylogenetic change of the evolving organism the selective strains are also continuously changing. As a consequence no state or invariant concept of economy can cover the different stages of the phylogenetic process. The pragmatical meaning of the theoretical consideration is substantiated by the example of the hydrostatic skeleton theory in which the chordates are derived from metameric worms with a fluid skeleton. Herrn Professor Dr. P. Dullemeijer sind die Verfasser für kritische Lektüre und wertovolle Hinweise zu Dank verpflichtet.     

Will changes in phenology track climate change? A study of growth initiation timing in coast Douglas‐fir

Under climate change, the reduction of frost risk, onset of warm temperatures and depletion of soil moisture are all likely to occur earlier in the year in many temperate regions. The resilience of tree species will depend on their ability to track these changes in climate with shifts in phenology that lead to earlier growth initiation in the spring. Exposure to warm temperatures (‘forcing’) typically triggers growth initiation, but many trees also require exposure to cool temperatures (‘chilling’) while dormant to readily initiate growth in the spring. If warming increases forcing and decreases chilling, climate change could maintain, advance or delay growth initiation phenology relative to the onset of favorable conditions. We modeled the timing of height‐ and diameter‐growth initiation in coast Douglas‐fir (an ecologically and economically vital tree in western North America) to determine whether changes in phenology are likely to track changes in climate using data from field‐based and controlled‐environment studies, which included conditions warmer than those currently experienced in the tree's range. For high latitude and elevation portions of the tree's range, our models predicted that warming will lead to earlier growth initiation and allow trees to track changes in the onset of the warm but still moist conditions that favor growth, generally without substantially greater exposure to frost. In contrast, toward lower latitude and elevation range limits, the models predicted that warming will lead to delayed growth initiation relative to changes in climate due to reduced chilling, with trees failing to capture favorable conditions in the earlier parts of the spring. This maladaptive response to climate change was more prevalent for diameter‐growth initiation than height‐growth initiation. The decoupling of growth initiation with the onset of favorable climatic conditions could reduce the resilience of coast Douglas‐fir to climate change at the warm edges of its distribution.