A long standing
goal in my laboratory has been to understand the neural mechanisms that allow
us to represent and identify spatial patterns. Our first line of research
concerned retinal adaptation mechanisms, which preserve spatial information
despite the enormous range of ambient light levels that occur in the natural
environment (e.g., Geisler, 1978a,b Vis. Res.; 1981, J Physio; 1983, Vis. Res.;
Hahn & Geisler, 1995; Kortum & Geisler, 1995). This work provided some
of the first psychophysical evidence (in detection and discrimination
experiments) for multiplicative, subtractive and response-saturation adaptation
mechanisms, and has helped to establish them as key components in
psychophysical models of light and dark adaptation. Our next line of research concerned
sequential ideal observer analysis (Geisler, 1984; Davila & Geisler, 1985;
Banks et al., 1987; Geisler, 1989; Arnow & Geisler, 1996). This work showed
that a number of interesting effects in human pattern detection and
discrimination can be explained by variations in the information available at
the level of the photoreceptor responses or at the level of the ganglion cell
responses (see also the button labeled Bayesian Ideal Observers).
More recent work (in collaboration
with Albrecht’s lab) has been concerned with cortical mechanisms of pattern
vision (Albrecht & Geisler, 1991; 1994; Geisler & Albrecht, 1992; 1997;
2001). Much of this work has been directed at developing a functional
quantitative description of the responses of single neurons in primary visual
cortex, with the aim of understanding how the population of cortical neurons
represents spatial and contrast information and how the responses of the
population contribute to the discrimination and identification performance of
the organism as a whole. The functional description of individual cortical
neurons that has emerged from our work and related work in the literature
consists of four components a linear filter (summation of excitation and
inhibition) that gives a cortical cell its basic stimulus selectivity, a
divisive contrast normalization mechanism that preserves selectivity while
producing response saturation, an expansive response exponent that enhances the
selectivity, and a noise mechanism that makes the variance of the response proportional
to the mean response. Although the responses of cortical neurons are
well-described by these mechanisms there is a great deal of heterogeneity from
cell to cell in the parameters of linear filter and in the parameters of the
non-linear contrast normalization and response exponent. To characterize this
heterogeneity we have extracted, from our large database of single cell
recordings, probability distributions (across cells) for the parameter values
describing the linear and non-linear mechanisms. Using these probability
distributions we have created “neuron sampling models,” which allow us to
simulate the population response of primary visual cortex. We have found that
these models, which are based directly on the distributions of cortical cell properties,
predict behavioral detection and discrimination performance along a number of
fundamental stimulus dimensions.