Biology subjects

Barnett, M. A.

Publications and source records attributed to Barnett, M. A..

3 recordsLinked to original sources

bioRxiv2024

Temporal dynamics of human color processing measured using a continuous tracking task

We characterized the temporal dynamics of color processing using a continuous tracking paradigm by estimating temporal impulse response functions associated with tracking chromatic Gabor patches. We measured how the lag of these functions changes as a function of chromatic direction and contrast for stimuli in the LS cone contrast plane. In the same set of subjects, we also measured detection thresholds for stimuli with matched spatial, temporal, and chromatic properties. We created a model of tracking and detection performance to test if a common representation of chromatic contrast accounts for both measures. The model summarizes the effect of chromatic contrast over different chromatic directions through elliptical isoresponse contours, the shapes of which are contrast independent. The fitted elliptical isoresponse contours have essentially the same orientation in the detection and tracking tasks. For the tracking task, however, there is a striking reduction in sensitivity to signals originating in the S cones. The results are consistent with common chromatic mechanisms mediating performance on the two tasks, but with task-dependent relative weighting of signals from L and S cones.

neuroscience↗

bioRxiv2020

A Quadratic Model Captures the Human V1 Response to Variations in Chromatic Direction and Contrast

An important goal for vision science is to develop quantitative models for the representation of visual signals at post-receptoral sites. To this end, we develop the quadratic color model (QCM) and examine its ability to account for the BOLD fMRI response in human V1 to spatially-uniform temporal chromatic modulations, systematically varying in their chromatic directions and contrasts. We find that the QCM explains the same, cross-validated variance as a conventional GLM, with far fewer free parameters. The QCM generalizes to allow prediction of V1 responses to a large range of modulations. We replicated the results for each subject and find good agreement across both replications and subjects. We find that within the LM cone contrast plane, V1 is most sensitive to L-M contrast modulations and least sensitive to L+M contrast modulations. Within V1, we observe little to no change in chromatic sensitivity as a function of eccentricity.

neuroscience↗

bioRxiv2020

Sulcal depth in medial ventral temporal cortex predicts the location of a place-selective region in macaques, children, and adults.

The evolution and development of anatomical-functional relationships in the cerebral cortex is of major interest in neuroscience. Here, we leveraged the fact that a functional region selective for visual scenes is located within a sulcus in medial ventral temporal cortex (VTC) in both humans and macaques to examine the relationship between sulcal depth and place-selectivity in medial VTC across species and age groups. To do so, we acquired anatomical and functional magnetic resonance imaging scans in 9 macaques, 26 human children, and 28 human adults. Our results revealed a strong structural-functional coupling between sulcal depth and place-selectivity across age groups and species in which selectivity was strongest at the deepest sulcal point (the sulcal pit). Interestingly, this coupling between sulcal depth and place-selectivity strengthens from childhood to adulthood in humans. Morphological analyses suggest that the stabilization of sulcal-functional coupling in adulthood may be due to sulcal deepening and areal expansion with age as well as developmental differences in cortical curvature at the pial, but not the white matter surfaces. Our results implicate sulcal features as functional landmarks in high-level visual cortex and highlight that sulcal-functional relationships in medial VTC are preserved between macaques and humans despite differences in cortical folding.

neuroscience↗