Bibliographie générale

List Resources

Displaying 1 - 1 of 1 (Bibliography: WIKINDX Master Bibliography)
Order by:

Ascending
Descending
Use all checked: 
Use all displayed: 
Use all in list: 
Levins, R., & Lewontin, R. C. (1985). The dialectical biologist. Harvard: Harvard University Press.  
Last edited by: Dominique Meeùs 2020-03-03 15:30:17 Pop. 0%
      A second consequence of the heterogeneity of all objects is that it directs us toward the explanation of change in terms of the opposing processes united within that object. Heterogeneity is not merely diversity: the parts or processes confront each other as opposites, conditional on the whole of which they are parts. For example, in the predator-prey system of lemmings and owls, the two species are opposite poles of the process, predation simultaneously determining the death rate of lemmings and the birth rate of owls. It is not that lemmings are the opposite of owls in some ontological sense, or that lemmings imply owls or couldn’t exist without owls. But within the context of this particular ecosystem, their interaction helps to drive the population dynamics, which shows a spectacular fluctuation of numbers.
     What characterizes the dialectical world, in all its aspects, as we have described it is that it is constantly in motion. Constants become variables, causes become effects, and systems develop, destroying the conditions that gave rise to them. Even elements that appear to be stable are in a dynamic equilibrium of forces that can suddenly become unbalanced, as when a dull gray lump of metal of a critical size becomes a fireball brighter than a thousand suns. Yet the motion is not unconstrained and uniform. Organisms develop and differentiate, then die and disintegrate. Species arise but inevitably become extinct. Even in the simple physical world we know of no uniform motion. Even the earth rotating on its axis has slowed down in geologic time. The development of systems through time, then, seems to be the consequence of opposing forces and opposing motions.
     This appearance of opposing forces has given rise to the most debated and difficult, yet the most central, concept in dialectical thought, the principle of contradiction. For some, contradiction is an epistemic principle only. It describes how we come to understand the world by a history of antithetical theories that, in contradiction to each other and in contradiction to observed phenomena, lead to a new view of nature. Kuhn’s (1962) theory of scientific revolution has some of this flavor of continual contradiction and resolution, giving way to new contradiction. For others, contradiction is not only epistemic but political as well, the contradiction between classes being the motive power of history. Thus contradiction becomes an ontological property at least of human social existence. For us, contradiction is not only epistemic and political, but ontological in the broadest sense. Contradictions between forces are everywhere in nature, not only in human social institutions. This tradition of dialectics goes back to Engels (1880) who wrote, in Dialectics of Nature, that “to me there could be no question of building the laws of dialectics of nature, but of discovering them in it and evolving them from it.” Engels’s understanding of the physical world was, of course, a nineteenth-century understanding, and much of what he wrote about it seems quaint. Moreover, dialecticians have repeatedly attempted to make the identification of contradictions in nature a central feature of science, as if all scientific problems are solved when the contradictions have been revealed. Yet neither Engels’ factual errors nor the rigidity of idealist dialectics changes the fact that opposing forces lie at the base of the evolving physical and biological world.
     Things change because of the actions of opposing forces on them, and things are the way they are because of the temporary balance of opposing forces. In the early days of biology an inertial view prevailed: nerve cells were at rest until stimulated by other nerve cells and ultimately by sensory excitation. Genes acted if the raw materials for their activity were present; otherwise they were quiescent. Gene frequencies in a population remained static in the absence of selection, mutation, random drift, or immigration. Nature was at equilibrium unless perturbed. Later it was recognized that nerve impulses act both to excite and to inhibit the firing of other nerves, so the state of a system depends on the network of opposing stimuli, and that network can generate spontaneous activity. Gene action is regulated by repressors, repressors of the repressors, and all sorts of active feedbacks in the cell. There are no genetic loci immune to mutation and random drift, and no populations are free of selection.
     The dialectical view insists that persistence and equilibrium are not the natural state of things but require explanation, which must be sought in the actions of the opposing forces.
wikindx 6.2.0 ©2003-2020 | Total resources: 1310 | Username: -- | Bibliography: WIKINDX Master Bibliography | Style: American Psychological Association (APA) | Database queries: 24 | DB execution: 0.01194 secs | Script execution: 0.06312 secs