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Holism and Reductionism in Biology and Ecology: The Mutual by Rick C. Looijen

By Rick C. Looijen

Holism and reductionism are generally visible as incompatible perspectives or ways to nature. the following Looijen argues that they need to otherwise be visible as collectively based and for this reason co-operating learn programmes. He sheds a few attention-grabbing new gentle at the emergence thesis, its relation to the aid thesis, and at the function and standing of useful causes in biology. He discusses a number of examples of aid in either biology and ecology, displaying the mutual dependence of holistic and reductionist examine programmes. Ecologists are provided separate chapters, clarifying a few significant, but hugely and arguable ecological strategies, akin to `community', `habitat', and `niche'. The publication is the 1st in-depth examine of the philosophy of ecology.
Readership: experts within the philosophy of technology, particularly the philosophy of biology, biologists and ecologists drawn to the philosophy in their self-discipline. additionally of curiosity to different scientists thinking about the holism-reductionism issue.

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Extra resources for Holism and Reductionism in Biology and Ecology: The Mutual Dependence of Higher and Lower Level Research Programmes

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In contrast to the other steps, the approximation step is not a deductive step, but a step in which the law or theory to be reduced is derived approximately. 1, approximative reductions involve some sort of correction of the reduced law or theory. In terms of Schaffner's (1967, 1993a,b) model, if Tl is the reducing theory and T2 the law or theory to be reduced, one deductively derives from Tl a corrected version ofT2, T2*, which can then be reduced to T2 only by approximation. From Newton's theory of gravitation (Tl) one can deductively derive a corrected version of Galileo's law of free fall (L2*: 34 CHAPTER 2 a(p) = M/[R + h(t)J2) which can be reduced to Galileo's law (L2: a(p) = MIR2) only by approximation.

Thus, according to Schaffner, replacement reductions can be reconstructed as the correction ofT2 by T2* (approximative reduction) and the subsequent (deductive) reduction ofT2* to (by) Tl (see also Schaffner 1993a,b). I will return to this later, when discussing Kuipers's reduction model. Though one might get the impression that replacement reductions are always ofthe homogeneous, domain-preserving type, this is not the case. For there are also many heterogeneous reductions in which, besides REDUCTION OF LAWS AND THEORIES 29 deductive steps, an approximation step occurs (see below).

One particularly well known vitalist was Hans Driesch (1909, 1914, 1927) who became famous for his experiments on sea-urchin eggs and who claimed he was able to explain the embryonic development of these eggs by the directive operation of a vital force. I will not dwell on this, because vitalism is practically a dead issue in biology today. Once in a while certain ideas or theories emerge that bear a certain resemblance to vitalism, such as Sheldrake's (1981) theory of morphogenetic fields, but these happen not to be taken seriously by the majority of other biologists.

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