The neocortex is the most characteristic feature of the human brain. On gross inspection, its convoluted surfaces can be seen to have overgrown and covered most other brain structures. In the functional sphere, it is to the neocortex that we attribute those behaviors assumed to be most uniquely human such as cognition and linguistic behavior. This essay is an attempt to understand how this structure expanded during the course of mammalian evolution. At present, any attempt must be more speculative than definitive, but it is offered in the hope that it will generate more discussion on a topic that is central to all neurobiology, as well as a number of allied disciplines. I will proceed by outlining current views on the evolution of the brain, briefly review the organization of the somatosensory cortex in several mammalian forms, and then discuss in some detail ontogenetic mechanisms that may have some bearing on neocortical phylogeny. The primary proposition put forth is that the mammalian neocortex is relatively unspecified by strict genetic means, and that this allowed the neocortex to expand and adapt to a variety of circumstances during the course of phylogeny.

The demonstration that functional somatotopic maps within the adult neocortex undergo some degree of reorganization following peripheral injury has aroused considerable interest. The evidence for such reorganization in the rat and monkey is reviewed and it is concluded that in both species there is good evidence for limited functional map reorganization in the adult neocortex following peripheral injury. The significance of such functional map reorganization, particularly in terms of whether or not cortical maps are continuously modifiable throughout life, is discussed. It is concluded that the current evidence for map reorganization is best interpreted in terms of the unmasking of preexisting neuronal circuits rather than as evidence of dynamic cortical selection processes.