@article {103, title = {Spatial and Temporal Structure of Receptive Fields in Primate Somatosensory Area 3b: Effects of Stimulus Scanning Direction and Orientation}, journal = {The Journal of Neuroscience}, volume = {20}, year = {2000}, month = {01/2000}, pages = {495 - 510}, abstract = {

This is the third in a series of studies of the neural representation of tactile spatial form in somatosensory cortical area 3b of the alert monkey. We previously studied the spatial structure of \>350 fingerpad receptive fields (RFs) with random-dot patterns scanned in one direction (DiCarlo et al., 1998) and at varying velocities (DiCarlo and Johnson, 1999). Those studies showed that area 3b RFs have a wide range of spatial structures that are virtually unaffected by changes in scanning velocity. In this study, 62 area 3b neurons were studied with three to eight scanning directions (58 with four or more directions). The data from all three studies are described accurately by an RF model with three components: (1) a single, central excitatory region of short duration, (2) one or more inhibitory regions, also of short duration, that are adjacent to and nearly synchronous with the excitation, and (3) a region of inhibition that overlaps the excitation partially or totally and is temporally delayed with respect to the first two components. The mean correlation between the observed RFs and the RFs predicted by this three-component model was 0.81. The three-component RFs also predicted orientation sensitivity and preferred orientation to a scanned bar accurately. The orientation sensitivity was determined most strongly by the intensity of the coincident RF inhibition in relation to the excitation. Both orientation sensitivity and this ratio were stronger in the supragranular and infragranular layers than in layer IV.

}, keywords = {Action Potentials, Animals, Discrimination Learning, Fingers, Macaca mulatta, Movement, Normal Distribution, Reaction Time, Somatosensory Cortex, Space Perception, Time Factors, Touch}, issn = {0270-6474}, doi = {10.1523/JNEUROSCI.20-01-00495.2000}, url = {http://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.20-01-00495.2000}, author = {DiCarlo, James J. and Johnson, Kenneth O.} } @article {107, title = {Velocity Invariance of Receptive Field Structure in Somatosensory Cortical Area 3b of the Alert Monkey}, journal = {The Journal of Neuroscience}, volume = {19}, year = {1999}, month = {01/1999}, pages = {401 - 419}, abstract = {

This is the second in a series of studies of the neural representation of tactile spatial form in cortical area 3b of the alert monkey. We previously studied the spatial structure of 330 area 3b neuronal receptive fields (RFs) on the fingerpad with random dot patterns scanned at one velocity (40 mm/sec;\ DiCarlo et al., 1998). Here, we analyze the temporal structure of 84 neuronal RFs by studying their spatial structure at three scanning velocities (20, 40, and 80 mm/sec). As in the previous study, most RFs contained a single, central, excitatory region and one or more surrounding or flanking inhibitory regions. The mean time delay between skin stimulation and its excitatory effect was 15.5 msec. Except for differences in mean rate, each neuron\’s response and the spatial structure of its RF were essentially unaffected by scanning velocity. This is the expected outcome when excitatory and inhibitory effects are brief and synchronous. However, that interpretation is consistent neither with the reported timing of excitation and inhibition in somatosensory cortex nor with the third study in this series, which investigates the effect of scanning direction and shows that one component of inhibition lags behind excitation. We reconcile these observations by showing that overlapping (in-field) inhibition delayed relative to excitation can produce RF spatial structure that is unaffected by changes in scanning velocity. Regardless of the mechanisms, the velocity invariance of area 3b RF structure is consistent with the velocity invariance of tactile spatial perception (e.g., roughness estimation and form recognition).

}, keywords = {Adaptation, Animals, Brain Mapping, Cortical Synchronization, Evoked Potentials, Female, Macaca mulatta, Male, Neural Inhibition, Physiological, Somatosensory Cortex, Visual Fields}, issn = {0270-6474}, doi = {10.1523/JNEUROSCI.19-01-00401.1999}, url = {http://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.19-01-00401.1999}, author = {DiCarlo, James J. and Johnson, Kenneth O.} } @article {110, title = {Structure of Receptive Fields in Area 3b of Primary Somatosensory Cortex in the Alert Monkey}, journal = {The Journal of Neuroscience}, volume = {18}, year = {1998}, month = {04/1998}, pages = {2626 - 2645}, abstract = {

We investigated the two-dimensional structure of area 3b neuronal receptive fields (RFs) in three alert monkeys. Three hundred thirty neurons with RFs on the distal fingerpads were studied with scanned, random dot stimuli. Each neuron was stimulated continuously for 14 min, yielding 20,000 response data points. Excitatory and inhibitory components of each RF were determined with a modified linear regression algorithm. Analyses assessing goodness-of-fit, repeatability, and generality of the RFs were developed. Two hundred forty-seven neurons yielded highly repeatable RF estimates, and most RFs accounted for a large fraction of the explainable response of each neuron. Although the area 3b RF structures appeared to be continuously distributed, certain structural generalities were apparent. Most RFs (94\%) contained a single, central region of excitation and one or more regions of inhibition located on one, two, three, or all four sides of the excitatory center. The shape, area, and strength of excitatory and inhibitory RF regions ranged widely. Half the RFs contained almost evenly balanced excitation and inhibition. The findings indicate that area 3b neurons act as local spatiotemporal filters that are maximally excited by the presence of particular stimulus features. We believe that form and texture perception are based on high-level representations and that area 3b is an intermediate stage in the processes leading to these representations. Two possibilities are considered: (1) that these high-level representations are basically somatotopic and that area 3b neurons amplify some features and suppress others, or (2) that these representations are highly transformed and that area 3b effects a step in the transformation.

}, keywords = {Afferent, Animals, Data Interpretation, Electrophysiology, Female, Macaca mulatta, Male, Neural Inhibition, Neurons, Reproducibility of Results, Somatosensory Cortex, Statistical, Touch}, issn = {0270-6474}, doi = {10.1523/JNEUROSCI.18-07-02626.1998}, url = {http://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.18-07-02626.1998}, author = {DiCarlo, James J. and Johnson, Kenneth O. and Hsiao, Steven S.} } @article {116, title = {Marking microelectrode penetrations with fluorescent dyes}, journal = {Journal of Neuroscience Methods}, volume = {64}, year = {1996}, month = {01/1996}, pages = {75 - 81}, abstract = {

Fluorescent dyes were used to mark and identify the tracks left by extracellular microelectrodes in neurophysiological experiments. Forty-two penetrations were made into the postcentral gyrus of 3 Macaque monkeys with electrodes coated with 1 of 5 fluorescent dyes (Dil, DiO, DiI-C5, PyPO, and Fast Blue). The electrodes were driven at rates ranging from 10 to 1000 \μm/min, to a depth of about 4000 \μm, where a small electrolytic lesion was made. Histological sections were viewed under fluorescent optics and the electrode tracks were reconstructed from the dye traces. Fluorescent traces (width 50\–400 \μm) were observed in 41 of 42 penetrations with 24 traces extending to the lesion site. Of the electrodes driven in less than 3 h, those coated with DiI (88) and DiI-C5 (88) left a trace to the lesion site, while 57\% (47) of the DiO, 40\% (25) of the Fast Blue and only 11\% (19) of the PyPO tracks were fully marked.

This method of marking penetrations can be used with any extracellular recording configuration, does not require tissue sections to be processed or stained, does not require electrical lesions, and causes no detectable tissue damage. Because the dyes fluoresce at different wavelengths, closely spaced tracks can be uniquely identified.

}, keywords = {Animals, Brain, Electrophysiology, Fluorescent Dyes, Macaca mulatta, Microelectrodes, Neurosciences}, issn = {01650270}, doi = {10.1016/0165-0270(95)00113-1}, url = {https://linkinghub.elsevier.com/retrieve/pii/0165027095001131}, author = {DiCarlo, James J. and Lane, John W. and Hsiao, Steven S. and Johnson, Kenneth O.} }