It is easy to conceive of a high degree of specificity in the brain when you remember that it contains one million million cells. If you lined up one million million periods of the size shown here next to one another, the line would stretch around the circumference of the earth almost twelve and a half times. After hearing about simple and complex cells, people often complain that the analysis of every tiny part of our visual field--for all possible orientations and for dark lines, light lines, and edges--must surely require an astronomic number of cells. The answer is yes, certainly. But that fits perfectly, because an astronomic number of cells is just what the cortex has. Today we can say what the cells in this part of the brain are doing, at least in response to many simple, everyday visual stimuli. I suspect that no two striate cortical cells do exactly the same thing, because whenever a microelectrode tip succeeds in recording from two cells at a time, the two show slight differences--in exact receptive field position, directional selectivity, strength of response, or some other attribute. In short, there seems to be little redundancy in this part of the brain. How sure can we be that these cells are not wired up to respond to some other stimulus besides straight line segments? It is not as though we and others have not tried many other stimuli, including faces, Cosmopolitan covers, and waving our hands. Experience shows that we would be foolish to think that we had exhausted the list of possibilities. In the early 1960s, just when we felt satisfied with the striate cortex and wanted to move on to the next area (in fact, we had moved on), we happened to record from a sluggishly responding cell in the striate cortex and, by making the slit shorter, found that this very cell was anything but a sluggish responder. In this way we stumbled on end stopping. And it took almost twenty years' work with the monkey striate cortex before we became aware of blobs--pockets of cells specialized for color, described in Chapter 8. Having expressed these reservations, I should add that I have no doubt at all that some of the findings, such as orientation selectivity, are genuine properties of these cells. There is too much collateral evidence, such as the functional anatomy, described in Chapter 5, to allow for much scepticism.