I hope to show that supervenience and determination, as I have here intuitively characterized them, are really different expressions of the same core idea which one may make more precise in a great number of different ways, depending on the interpretation one puts on the catchall parameters “cases”, “truth of kind P”and “truth of kind S”.

We develop an account of laboratory models, which have been central to the group selection controversy. We compare arguments for group selection in nature with Darwin's arguments for natural selection to argue that laboratory models provide important grounds for causal claims about selection. Biologists get information about causes and cause-effect relationships in the laboratory because of the special role their own causal agency plays there. They can also get information about patterns of effects and antecedent conditions in nature. But to (...) argue that some cause is actually responsible in nature, they require an inference from knowledge of causes in the laboratory context and of effects in the natural context. This process, cause detection, forms the core of an analogical argument for group selection. We discuss the differing roles of mathematical and laboratory models in constructing selective explanations at the group level and apply our discussion to the units of selection controversy to distinguish between the related problems of cause determination and evaluation of evidence. Because laboratory models are at the intersection of the two problems, their study is crucial for framing a coherent theory of explanation for evolutionary biology. (shrink)

According to a doctrine that has been popularized by Kripke and Putnam, a natural kind term like 'bird' rigidly designates the kind with the microstructure of sample birds. This microstructure is the essence of birdhood, so our learning what the relevant microstructure is our discovery of the kind's essence. We have discovered that some statement like 'The bird is the taxon with such and such DNA structure' is true. Further, it is commonly added, the discovered microstructure is essential to each (...) particular bird. ;I argue that this general picture is mistaken. I do accept and defend the view that terms like 'bird' are rigid designators. However, the picture at issue has other difficulties. Individual birds are not essentially birds. And the view that biologists have discovered or will discover that the bird kind is identical to some DNA structure or other type of structure seems wrong. We don't discover just what particular characteristic a kind is to be identified with. Rather, the meaning of natural kind terms changes; as science advances, more sophisticated concepts attending kind terms replace older ones. So the Kripke-Putnam account of our discovering the truth of theoretical identity statements seems wrong. ;Fortunately, the account retains some interest despite its falsity, because of its association with the claim that statements like 'The bird is the taxon with such and such DNA structure' are necessary but a posteriori. The above sentence does not express a truth, much less a necessary truth, but the idea that it could have expressed the sort of necessary a posteriori truth it is supposed to express is epistemologically interesting. The very possibility of such necessary a posteriori knowledge deserves some account. I offer an account, arguing that this sort of knowledge is no more impressive from an epistemological standpoint than is knowledge of analytic necessity: indeed, I argue, it is best understood as knowledge of a species of analytic necessity. Independently of this claim, I argue in a concluding discussion that analyticity ought to be accepted by proponents of the necessary theoretical identity statements in question. (shrink)