Changes in neural readout of response magnitude during auditory streaming do not correlate with behavioral choice in the auditory cortex.

A fundamental goal of the auditory system is to group stimuli from the auditory environment into a perceptual unit (i.e., "stream") or segregate the stimuli into multiple different streams. Although previous studies have clarified the psychophysical and neural mechanisms that may underlie this ability, the relationship between these mechanisms remains elusive. Here, we recorded multiunit activity (MUA) from the auditory cortex of monkeys while they participated in an auditory-streaming task consisting of interleaved low- and high-frequency tone bursts. As the streaming stimulus unfolded over time, MUA amplitude habituated; the magnitude of this habituation was correlated with the frequency difference between the tone bursts. An ideal-observer model could classify these time- and frequency-dependent changes into reports of "one stream" or "two streams" in a manner consistent with the behavioral literature. However, because classification was not modulated by the monkeys' behavioral choices, this MUA habituation may not directly reflect perceptual reports.

Computational and neurophysiological principles underlying auditory perceptual decisions.

A fundamental scientific goal in auditory neuroscience is identifying what mechanisms allow the brain to transform an unlabeled mixture of auditory stimuli into distinct perceptual representations. This transformation is accomplished by a complex interaction of multiple neurocomputational processes, including Gestalt grouping mechanisms, categorization, attention, and perceptual decision-making. Despite a great deal of scientific energy devoted to understanding these principles of hearing, we still do not understand either how auditory perception arises from neural activity or the causal relationship between neural activity and auditory perception. Here, we review the contributions of cortical and subcortical regions to auditory perceptual decisions with an emphasis on those studies that simultaneously measure behavior and neural activity. We also put forth challenges to the field that must be faced if we are to further our understanding of the relationship between neural activity and auditory perception.

Sound Frequency Representation in the Auditory Cortex of the Common Marmoset Visualized Using Optical Intrinsic Signal Imaging.

Natural sound is composed of various frequencies. Although the core region of the primate auditory cortex has functionally defined sound frequency preference maps, how the map is organized in the auditory areas of the belt and parabelt regions is not well known. In this study, we investigated the functional organizations of the core, belt, and parabelt regions encompassed by the lateral sulcus and the superior temporal sulcus in the common marmoset (Callithrix jacchus). Using optical intrinsic signal imaging, we obtained evoked responses to band-pass noise stimuli in a range of sound frequencies (0.5-16 kHz) in anesthetized adult animals and visualized the preferred sound frequency map on the cortical surface. We characterized the functionally defined organization using histologically defined brain areas in the same animals. We found tonotopic representation of a set of sound frequencies (low to high) within the primary (A1), rostral (R), and rostrotemporal (RT) areas of the core region. In the belt region, the tonotopic representation existed only in the mediolateral (ML) area. This representation was symmetric with that found in A1 along the border between areas A1 and ML. The functional structure was not very clear in the anterolateral (AL) area. Low frequencies were mainly preferred in the rostrotemplatal (RTL) area, while high frequencies were preferred in the caudolateral (CL) area. There was a portion of the parabelt region that strongly responded to higher sound frequencies (>5.8 kHz) along the border between the rostral parabelt (RPB) and caudal parabelt (CPB) regions.

Representation of Glossy Material Surface in Ventral Superior Temporal Sulcal Area of Common Marmosets.

The common marmoset (Callithrix jacchus) is one of the smallest species of primates, with high visual recognition abilities that allow them to judge the identity and quality of food and objects in their environment. To address the cortical processing of visual information related to material surface features in marmosets, we presented a set of stimuli that have identical three-dimensional shapes (bone, torus or amorphous) but different material appearances (ceramic, glass, fur, leather, metal, stone, wood, or matte) to anesthetized marmoset, and recorded multiunit activities from an area ventral to the superior temporal sulcus (STS) using multi-shanked, and depth resolved multi-electrode array. Out of 143 visually responsive multiunits recorded from four animals, 29% had significant main effect only of the material, 3% only of the shape and 43% of both the material and the shape. Furthermore, we found neuronal cluster(s), in which most cells: (1) showed a significant main effect in material appearance; (2) the best stimulus was a glossy material (glass or metal); and (3) had reduced response to the pixel-shuffled version of the glossy material images. The location of the gloss-selective area was in agreement with previous macaque studies, showing activation in the ventral bank of STS. Our results suggest that perception of gloss is an important ability preserved across wide range of primate species.

Mirror Neurons in a New World Monkey, Common Marmoset.

Mirror neurons respond when executing a motor act and when observing others' similar act. So far, mirror neurons have been found only in macaques, humans, and songbirds. To investigate the degree of phylogenetic specialization of mirror neurons during the course of their evolution, we determined whether mirror neurons with similar properties to macaques occur in a New World monkey, the common marmoset (Callithrix jacchus). The ventral premotor cortex (PMv), where mirror neurons have been reported in macaques, is difficult to identify in marmosets, since no sulcal landmarks exist in the frontal cortex. We addressed this problem using "in vivo" connection imaging methods. That is, we first identified cells responsive to others' grasping action in a clear landmark, the superior temporal sulcus (STS), under anesthesia, and injected fluorescent tracers into the region. By fluorescence stereomicroscopy, we identified clusters of labeled cells in the ventrolateral frontal cortex, which were confirmed to be within the ventrolateral frontal cortex including PMv after sacrifice. We next implanted electrodes into the ventrolateral frontal cortex and STS and recorded single/multi-units under an awake condition. As a result, we found neurons in the ventrolateral frontal cortex with characteristic "mirror" properties quite similar to those in macaques. This finding suggests that mirror neurons occur in a common ancestor of New and Old World monkeys and its common properties are preserved during the course of primate evolution.

Functional columns in superior temporal sulcus areas of the common marmoset.

Cortical areas in the superior temporal sulcus (STS) of primates have been recognized as a part of the 'social brain'. In particular, biological motion stimuli elicit neuronal responses in the STS, indicating their roles in the ability to understand others' actions. However, the spatial organization of functionally identified STS cells is not well understood because it is difficult to identify the precise locations of cells in sulcal regions. Here, using a small New World monkey, the common marmoset (Callithrix jacchus) that has a lissencephalic brain, we investigated the spatial organization of the cells responsive to other's actions in STS. The neural responses to movies showing several types of other's actions were recorded with multicontact linear-array electrodes that had four shanks (0.4 mm spacing), with eight electrode contacts (0.2 mm spacing) for each shank. The four shanks were penetrated perpendicular to the cortical surface. We found that STS cells significantly responded to other's goal-directed actions, such as when an actor marmoset was reaching for and grasping a piece of food. The response profiles to the movies were more similar between the vertically positioned electrodes than horizontally positioned electrodes when the distances between electrodes were matched. This indicates that there are functional columns in the higher-order visual areas in STS of the common marmoset.

Indifference of marmosets with prenatal valproate exposure to third-party non-reciprocal interactions with otherwise avoided non-reciprocal individuals.

Autism is characterized by deficits in social interaction and social recognition. Although animal models of autism have demonstrated that model animals engage less in social interaction or attend less to conspecifics than control animals, no animal model has yet replicated the deficit in recognition of complex social interaction as is seen in humans with autism. Here, we show that marmosets discriminated between human actors who reciprocated in social exchanges and those who did not; however, marmosets with foetal exposure to valproic acid (VPA marmosets) did not. In the reciprocal condition, two actors exchanged food equally, while in the non-reciprocal condition, one actor (non-reciprocator) ended up with all food and the other actor with none. After observing these exchanges, the control marmosets avoided receiving food from the non-reciprocator in the non-reciprocal condition. However, the VPA marmosets did not show differential preferences in either condition, suggesting that the VPA marmosets did not discriminate between reciprocal and non-reciprocal interactions. These results indicate that normal marmosets can evaluate social interaction between third-parties, while the VPA marmosets are unable to recognize whether an individual is being reciprocal or not. This test battery can serve as a useful tool to qualify primate models of autism.

Effects of luminance contrast on the color selectivity of neurons in the macaque area v4 and inferior temporal cortex.

Appearance of a color stimulus is significantly affected by the contrast between its luminance and the luminance of the background. In the present study, we used stimuli evenly distributed on the CIE-xy chromaticity diagram to examine how luminance contrast affects neural representation of color in V4 and the anterior inferior temporal (AITC) and posterior inferior temporal (PITC) color areas (Banno et al., 2011). The activities of single neurons were recorded from monkeys performing a visual fixation task, and the effects of luminance contrast on the color selectivity of individual neurons and their population responses were systematically examined by comparing responses to color stimuli that were brighter or darker than the background. We found that the effects of luminance contrast differed considerably across V4 and the PITC and AITC. In both V4 and the PITC, the effects of luminance contrast on the population responses of color-selective neurons depended on color. In V4, the size of the effect was largest for blue and cyan, whereas in the PITC, the effect gradually increased as the saturation of the color stimulus was reduced, and was especially large with neutral colors (white, gray, black). The pattern observed in the PITC resembles the effect of luminance contrast on color appearance, suggesting PITC neurons are closely involved in the formation of the perceived appearance of color. By contrast, the color selectivities of AITC neurons were little affected by luminance contrast, indicating that hue and saturation of color stimuli are represented independently of luminance contrast in the AITC.

Marmoset monkeys evaluate third-party reciprocity.

Many non-human primates have been observed to reciprocate and to understand reciprocity in one-to-one social exchanges. A recent study demonstrated that capuchin monkeys are sensitive to both third-party reciprocity and violation of reciprocity; however, whether this sensitivity is a function of general intelligence, evidenced by their larger brain size relative to other primates, remains unclear. We hypothesized that highly pro-social primates, even with a relatively smaller brain, would be sensitive to others' reciprocity. Here, we show that common marmosets discriminated between human actors who reciprocated in social exchanges with others and those who did not. Monkeys accepted rewards less frequently from non-reciprocators than they did from reciprocators when the non-reciprocators had retained all food items, but they accepted rewards from both actors equally when they had observed reciprocal exchange between the actors. These results suggest that mechanisms to detect unfair reciprocity in third-party social exchanges do not require domain-general higher cognitive ability based on proportionally larger brains, but rather emerge from the cooperative and pro-social tendencies of species, and thereby suggest this ability evolved in multiple primate lineages.

Reciprocal connectivity of identified color-processing modules in the monkey inferior temporal cortex.

The inferior temporal (IT) cortex is the last unimodal visual area in the ventral visual pathway and is essential for color discrimination. Recent imaging and electrophysiological studies have revealed the presence of several distinct patches of color-selective cells in the anterior IT cortex (AIT) and posterior IT cortex (PIT). To understand the neural machinery for color processing in the IT cortex, in the present study, we combined anatomical tracing methods with electrophysiological unit recordings to investigate the anatomical connections of identified clusters of color-selective cells in monkey IT cortex. We found that a color cluster in AIT received projections from a color cluster in PIT as well as from discrete clusters of cells in other occipitotemporal areas, in the superior temporal sulcus, and in prefrontal and parietal cortices. The distribution of the labeled cells in PIT closely corresponded with that of the physiologically identified color-selective cells in this region. Furthermore, retrograde tracer injections in the posterior color cluster resulted in labeled cells in the anterior cluster. Thus, temporal lobe color-processing modules form a reciprocally interconnected loop within a distributed network.

Color selectivity of neurons in the posterior inferior temporal cortex of the macaque monkey.

We recorded the activities of neurons in the lateral surface of the posterior inferior temporal cortex (PIT) of 3 hemispheres of 3 monkeys performing a visual fixation task. We characterized the color and shape selectivities of each neuron, mapped its receptive field (RF), and studied the distributions of these response properties. Using a set of color stimuli that were systematically distributed in Commission Internationale de l'Eclairage-xy chromaticity diagram, we found numerous color-selective neurons distributed throughout the area examined. Neurons in the ventral region tended to have sharper color tuning than those in the dorsal region. We also found a crude retinotopic organization in the ventral region. Within the ventral region of PIT, neurons in the dorsal part had RFs that overlapped the foveal center; the eccentricity of RFs increased in the more ventral part, and neurons in the anterior and posterior parts had RFs that represented the lower and upper visual fields, respectively. In all 3 hemispheres, the region where sharply tuned color-selective neurons were concentrated was confined within this retinotopic map. These findings suggest that PIT is a heterogeneous area and that there is a circumscribed region within it that has crude retinotopic organization and is involved in the processing of color.