There is a tendency in contemporary (analytic) aesthetics to consider- ably restrict the scope of things that can be beautiful or ugly. This peculiarly modern tendency is holding back progress in aesthetics and robbing it of its potential contribution to other domains of inquiry. One view that has suffered neglect as a result of this tendency is the moral beauty view, whereby the moral virtues are beautiful and the moral vices are ugly. This neglect stems from an assumption to the (...) effect that virtues and vices simply cannot be beautiful or ugly. The aim of this paper is twofold. First, it develops an account of form, under which, it argues, possession of form suffices for an object’s candidature for beauty and ugliness. Second, it argues that, under the foregoing proposal, the moral beauty view turns out to be a coherent position, and so should be taken seriously in both aesthetics and ethics. (shrink)

Discussions of the functions of biological traits generally take the notion of a trait for granted. Defining this notion is a non-trivial problem. Different approaches to function place different constraints on adequate accounts of the notion of a trait. Accounts of function based on engineering-style analyses allow trait boundaries to be a matter of human interest. Accounts of function based on natural selection have typically been taken to require trait boundaries that are objectively real. After canvassing problems raised by each (...) approach, I conclude with some facts that satisfactory notions of trait must respect. (shrink)

This paper offers an account of the relationship between inference and explanation in functional morphology which combines Robert Brandon's theory of adaptation explanation with standard accounts of inference to the best explanation. Inferences of function from structure, it is argued, are inferences to the best adaptation explanation. There are, however, three different approaches to the problem of determining which adaptation explanation is the best. The theory of inference to the best adaptation explanation is then applied to a case study from (...) the history of functional morphology: the case of the crested duckbilled dinosaurs. (shrink)

In this study the relationship between functional morpholoy and evolutionary biology is analysed by confronting the main concepts in both disciplines.Rather than only discussing this connection theoretically, the analysis is carried out by introducing important practical and experimental studies, which use aspects from both disciplines. The mentioned investigations are methodologically analysed and the consequences for extensions of the relationship are worked out. It can be shown that both disciplines have a large domain of their own and also share a large (...) common ground. Many disagreements among evolutionary biologists can be reduced to differences in general philosophy (idealism vs. realism), selection of phenomenona (structure vs. function), definition of concepts (natural selection) and the position of the concept theory as an explaining factor (neutralists vs. selectionists, random variation, determinate selection, etc.). (shrink)

Contrariando la concepción etiológica de las funciones biológicas, se pretende mostrar que las explicaciones por selección natural, lejos de justificar atribuciones funcionales, las presuponen; y que estas atribuciones pueden ser entendidas apelando a una especificación particular de la concepción s..

Many of us consider it uncontroversial that information processing is a natural function of the brain. Since functions in biology are only won through empirical investigation, there should be a significant body of unambiguous evidence that supports this functional claim. Before we can interpret the evidence, however, we must ask what it means for a biological system to process information. Although a concept of information is generally accepted in the neurosciences without critique, in other biological sciences applications of information, despite (...) careful analysis, remain controversial. In this work I will review classical stimulus-response studies in neuroscience and use Claude Shannon’s mathematical information theory as a starting point to interpret information processing as a function of the brain. I will illustrate a disanalogy between Shannon’s communication model (source, encode, channel, receiver, decode) and neural systems, and will argue that the neural code is not very code-like in comparison to genetic and engineered codes. I suggest that we have conflated the act of representing neuroscientific facts—which we do to summarize and communicate our findings with others—with taking experimental facts to be representations. (shrink)

Much of Stephen Jay Gould’s legacy is dominated by his views on the contingency of evolutionary history expressed in his classic Wonderful Life. However, Gould also campaigned relentlessly for a “nomothetic” paleontology. How do these commitments hang together? I argue that Gould’s conception of science and natural law combined with his commitment to contingency to produce an evolutionary science centered around the formulation of higher-level evolutionary laws.

Philosophers of biology have developed an extensive literature on biological functions. Here I propose a treatment of the topic based in social studies of science. I posit that the chief philosophical accounts of biological functions all rest upon a realist ontology of biological functions, one that conceives functions as human-independent qualities of things. Rather than being conceptualised as a property of traits or structures, function should be understood as a status granted by communities acting in accordance with specific domains of (...) knowledge and practice. Function becomes not a property of things, but a collective good: not of things, but by communities. I survey the existing explanations of biological functions from the philosophical literature and identify what I take to be those accounts’ shared complications. I then employ Martin Kusch’s communitarian epistemology as a point of departure for a sociological conception of function and develop an explanation of function that rests on an understan.. (shrink)

In this paper, I argue that the German morphological tradition made a major contribution to twentieth-century study of form. Several scientists paved the way for this research: paleontologist Adolf Seilacher, entomologist Hermann Weber, and biologist Johann-Gerhard Helmcke together with architect Frei Otto. All of them sought to examine morphogenetic processes to illustrate their inherent structural properties, thus challenging the neo-Darwinian framework of evolutionary theory. I point out that the German theoretical challenge to adaptationist thinking was possible through an exchange and (...) transfer of practices, data, technologies, and knowledge between biologically oriented students of form and architects, designers, and engineers. This exchange of practices and knowledge was facilitated by the establishment of two collaborative research centers at the beginning of the 1970s. Hence, by showing the richness of topics, methods, and technologies discussed in German-speaking morphology between 1950 and the 1970s, this paper paves the way to a much broader comprehension of the shifts that have shaped twentieth-century evolutionary biology. (shrink)

In a recent paper, Chris Haufe paints a provocative portrait of the late paleontologist Stephen Jay Gould. His principal aim is to resolve a “paradox” arising from a prima facie inconsistent pair of commitments: Gould believed that the biological facts could have been otherwise, and Gould believed that there are evolutionary laws. In order to resolve this paradox, Haufe makes two substantive claims: Gould was aware of the challenges that the Replay Thesis posed for a law-centered science of evolution, even (...) early in his career, and Gould endeavored to meet these challenges by deploying the “species-as-particles approach.” In this paper, I put pressure on both of these claims. By examining the goals and methods of Gould’s first “nomothetic research program,” the science of form, I show that it does not fit the picture of nomothetic science that Haufe illustrates. Additionally, I show that no straightforward connection exists between Gould’s understanding of contingency and his adoption of the species-as-particles approach. I propose that Gould’s career can be usefully split into three periods, each of which employed a distinct strategy for establishing distinctively paleontological contributions to evolutionary theory. (shrink)

From the early nineteenth century, the successful use of fossils in stratigraphy oriented paleontology towards geology. The consequent marginalising of biological objectives was countered in the twentieth century by the rise of ‘Paläobiologie’, first in the German cultural area and only later, as ‘paleobiology’, in the anglophone world. Several kinds of paleobiological research flourished internationally after the Second World War, among them the novel field of ‘paleoecology’. Within this field there were attempts to apply functional morphology to the problematical cases (...) of fossil organisms, for which functions cannot be observed directly. This article describes the origins of the kind of functional inference for fossils that I proposed in 1961 as the method of ‘paradigms’. Here I summarize some of my ‘worked exemplars’, which were intended to show the paradigm method in action. These case-studies were all taken from the paleontologically important phylum of the Brachiopoda, but the method was claimed to have much wider implications for the interpretation of the fossil record in terms of adaptive evolution. This article takes the history of the paradigm method as far as the late 1960s. I hope to trace, in a sequel, its ambivalent fate during the 1970s and beyond, when for example Gould’s critique of ‘the adaptationist programme’ and the rise of computer-based quantitative methods for the evolutionary interpretation of the fossil record led to the relative eclipse of functional morphology in paleontology. (shrink)

We identify a species of experiment—Kon-Tiki experiments—used to demonstrate the competence of a cause to produce a certain effect, and we examine their role in the historical sciences. We argue that Kon-Tiki experiments are used to test middle-range theory, to test assumptions within historical narratives, and to open new avenues of inquiry. We show how the results of Kon-Tiki experiments are involved in projective inferences, and we argue that reliance on projective inferences does not provide historical scientists with any special (...) protection against the problem of unconceived alternatives. (shrink)

Few of Stephen Jay Gould’s accomplishments in evolutionary biology have received more attention than his hierarchical theory of evolution, which postulates a causal discontinuity between micro- and macroevolutionary events. But Gould’s hierarchical theory was his second attempt to supply a theoretical framework for macroevolutionary studies—and one he did not inaugurate until the mid-1970s. In this paper, I examine Gould’s first attempt: a proposed fusion of theoretical morphology, multivariate biometry and the experimental study of adaptation in fossils. This early “macroevolutionary synthesis” (...) was predicated on the notion that parallelism and convergence dominate the history of higher taxa, and moreover, that they can be explained in terms of adaptation leading to mechanical improvement. In this paper, I explore the origins and contents of Gould’s first macroevolutionary synthesis, as well as the reasons for its downfall. In addition, I consider how various developments during the mid-1970s led Gould to identify hierarchy and constraint as the leading themes of macroevolutionary studies—and adaptation as a macroevolutionary red herring. (shrink)

It is shown in a literature review, that in the Typostrophic Theory autonomous mechanisms in the organism are considered as the factors which play a decisive role in orienting and controlling the evolutionary process. Selection is a controlling factor of only minor importance. The Synthetic Theory, on the other side, says that phylogenetic changes are not random or controlled by “internal factors” but can always be considered as adaptive remodellings. They are achieved by selection acting on the variation within populations. (...) Ecological, historical and “bautechnische” factors are considered as limiting mechanisms in the evolutionary process. They are discussed in detail in the text. (shrink)

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. (shrink)

Evolutionary change is opportunistic, but its course is strongly constrained in several fundamental ways. These constraints (historical/phylogenetic, functional/adaptive, constructional/morphogenetic) and their dynamic relationships are discussed here and shown to constitute the conceptual framework of Constructional Morphology. Notwithstanding recent published opinions which claim that the discovery of constraints renders Neodarwinian selection theory obsolete, we regard the insights of Constructional Morphology as being entirely consistent with this theory. As is shown here in the case of the Hyracoidea, formal analysis of the constraints (...) which have framed the evolution of various characters extends our understanding of the evolution of a taxon. (shrink)

An earlier article described the mid-twentieth century origins of the method of “paradigms” in paleobiology, as a way of making testable hypotheses about the functional morphology of extinct organisms. The present article describes the use of “paradigms” through the 1970s and, briefly, to the end of the century. After I had proposed the paradigm method to help interpret the ecological history of brachiopods, my students developed it in relation to that and other invertebrate phyla, notably in Euan Clarkson’s analysis of (...) vision in trilobites. David Raup’s computer-aided “theoretical morphology” was then combined with my functional or adaptive emphasis, in Adolf Seilacher’s tripartite “constructional morphology.” Stephen Jay Gould, who had strongly endorsed the method, later switched to criticizing the “adaptationist program” he claimed it embodied. Although the explicit use of paradigms in paleobiology had declined by the end of the century, the method was tacitly subsumed into functional morphology as “biomechanics.”. (shrink)

It is argued that the narrow concept of selection used since the time ofDarwin is only concerned with the relation between organism and its environment . It did not include the organism itself, which was the object of the pre-phylogenetic idealistic morphology. An adequate understanding of the mechanism of evolution dispenses with the concept of morphology as the basis of phylogeny.Es wird aufgezeigt, da\ der aufDarwin selbst zurückgehende eingeengte Gebrauch des Selektionskonzeptes auf die Beziehung zwischen Organismus und Umwelt die biologische (...) Konstruktion der vorphylogenetischen idealistischen Morphologie überlassen hat. Ein zutreffendes VerstÄndnis des Evolutionsmechanismus begreift aber die biologische Apparatur ein, entzieht der Morphologie, soweit sie sich als Vorbedingung phylogenetischen Arbeitens versteht, den Boden. (shrink)

Ecology is being introduced to Evolutionary Developmental Biology to enhance organism-, population-, species-, and higher-taxon-level studies. This exciting, bourgeoning troika will revolutionise how investigators consider relationships among environment, ontogeny, and phylogeny. Features are studied (and even defined) differently in ecology, development, and evolution. Form is central to development and evolution but peripheral to ecology. Congruence (i.e., homology) is applied at different hierarchical levels in the three disciplines. Function is central to ecology but peripheral to development. Herein, the supercategories form (‘isomorphic’ (...) or ‘allomorphic’), congruence (‘homologous’ or ‘homoplastic’), and function (‘adaptive’ or ‘nonadaptive’) are combined with two developmental mode (i.e., growth) categories (‘conformational’ or ‘nonconformational’) to provide a 16-class system for analysing features in studies in which ecology, development, and evolution are integrated. (shrink)

The idiom referred to in the title, “don't throw out the baby with the bath water,” instructs us to keep what is essential and to only throw away what is inessential. Bathing babies has the well-being of the child in mind, the end result of which is cleanliness. Efficiency in the task of cleaning is secondary. No one would throw away a baby when draining the baby's bathwater. Somewhat analogously, science and philosophy each have the goal of the attainment of (...) truth in mind. Part and parcel of this search for truth has been the attachment of being parsimonious, especially since William of Ockham. If the goal is truth, then one cannot get lost in the pursuit of parsimony, therefore losing the truth. The goal of finding the truth must remain intact; the method of parsimony at best remains subservient to the attainment of truth. Hans Jonas believed this regarding truth and pursued the criticism of reductive materialism as part and parcel of his research program in philosophy of biology and philosophical anthropology beginning in 1950. In his mind, reductive materialism, as it was practiced, involved the pursuit of parsimony at the cost of the truth through neglect of the purpose-driven conscious life of the subject. In this article, I expose and defend the recovery of certain elements of Aristotelian biology by Professor Hans Jonas. In the process, I show how Jonas was among the early authors writing on the philosophy of biology and defending ontological essentialism and purposefulness in organisms against reductive materialism and the relentless pursuit of the unity of the sciences. Along this line, I position Jonas among the arguments made regarding teleological explanations current in the philosophy of biology. First, I explain and defend Jonas's thesis that a full understanding of organisms requires recognizing an ontological essentialism regarding organisms. Secondly, I explain and defend Jonas's forward looking and backward looking teleological conceptions of activity insofar as it concurs directly with the conscious experience of life for humans, while situating it within the mainstream of philosophy of biology. Last, the importance of this recovery of Aristotelian concepts highlights Jonas's position as an early proponent of non-reductive materialism. More importantly, his thought forces us to recognize that in the pursuit of truth we must use parsimony well. We should take extreme care to preserve the truth; we should not throw out the baby with the bath water. (shrink)

An initial investigation of controversies and differences in opinion in the various schools of functional anatomy is presented by listing the methodology problems.The possibilities and limitations of functional anatomy are derived from the successive steps in the procedure in a functional anatomical investigation.Starting from the holistic approach as introduced byVan der Klaauw, the main problems of defining the term functional component and the applied methods are discussed.Two principal methods are presented, of which the limitations are considered. The various aspects where (...) new information is needed are illustrated in the example of bone mechanics. The advantages of an approach from a pattern of the interrelations are mentioned. (shrink)