1. Isolated, single-neuron extracellular potentials were recorded sequ
entially in area TE of the inferior temporal cortex (IT) of two macaqu
e monkeys (n = 58 and n = 41 neurons). Data were obtained while the an
imals were performing a paired-associate task. The task utilized five
stimuli and eight stimulus pairings (4 correct and 4 incorrect). Data
were evaluated as average spike rate during experimental epochs of 100
or 400 ms. Single-unit and population characteristics were measured u
sing a form of linear discriminant analysis and information theoretic
measures. To evaluate the significance of covariance on population cod
e measures, additional data consisting of simultaneous recordings from
less than or equal to 8 isolated neurons(n = 37) were obtained from a
third macaque monkey that was passively viewing visual stimuli. 2. On
average, 43% of IT neurons were activated by any of the stimuli used
(60% if those inhibited also are included). Yet the neurons were rathe
r unique in the relative magnitude of their responses to each stimulus
in the test set. These results suggest that information may be repres
ented in IT by the pattern of activity across neurons and that the rep
resentation is not sparsely coded. It is further suggested that the re
presentation scheme may have similarities to DNA or computer codes whe
rein a coding element is not a local parametric descriptor. This is a
departure from the V1 representation, which appears to be both local a
nd parametric. It is also different from theories of IT representation
that suggest a constructive basis set or ''alphabet''. From this view
, determination of stimurus discrimination capacity in IT should be ev
aluated by measures of population activity patterns. 3. Evaluation of
small groups of simultaneously recorded neurons obtained during a fixa
tion task suggests that little information about visual stimuli is con
veyed by covariance of activity in IT when a 100-ms time scale is used
as in this study. This finding is consistent with a prior report, by
Gochin et al., which used a I-ms time scare and failed to find neural
activity coherence or oscillations dependent on stimuli. 4. Population
-stimulus-discrimination capacity measures were influenced by the numb
er of neurons and to some extent the number and type of stimuli. 5. In
formation conveyed by individual neurons (mutual information) averaged
0.26 bits. The distribution of information values was uni-modal and i
s therefore more consistent with a distributed than a local coding sch
eme. Populations of neurons conveyed less information than the sum of
the individuals, reaching <1.9 bits for similar to 50 neurons, thus in
dicating considerable redundancy. The novelty of information was found
to be a function of the size of the population sample, apparently dec
reasing by 1/root n. 6. Information available through the course of th
e behavioral paradigm was evaluated by partitioning the data into 100-
ms epochs. The results indicate that a relatively large amount of info
rmation becomes available in the second 100 ms after stimulus onset. T
he peak in information occurs between 200 and 400 ms after stimulus on
set and significantly decays before the stimulus is removed. By the ti
me the second stimulus was shown in our paired associates paradigm (50
0 ms after stimulus 1 offset), information about the first stimulus wa
s about half of the peak value.