Fusiform activation to animals is driven by the process, not the stimulus

Previous studies have found that the lateral posterior fusiform gyri respond more robustly to pictures of animals than pictures of manmade objects and suggested that these regions encode the visual properties characteristic of animals. We suggest that such effects actually reflect processing demands arising when items with similar representations must be finely discriminated. In a positron emission tomography (PET) study of category verification with colored photographs of animals and vehicles, there was robust animal-specific activation in the lateral posterior fusiform gyri when stimuli were categorized at an intermediate level of specificity (e.g., dog or car). However, when the same photographs were categorized at a more specific level (e.g., Labrador or BMW), these regions responded equally strongly to animals and vehicles. We conclude that the lateral posterior fusiform does not encode domain-specific representations of animals or visual properties characteristic of animals. Instead, these regions are strongly activated whenever an item must be discriminated from many close visual or semantic competitors. Apparent category effects arise because, at an intermediate level of specificity, animals have more visual and semantic competitors than do artifacts

The contribution of fMRI in the study of visual categorization and expertise

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Neural correlates of the processing of co-speech gestures

In communicative situations, speech is often accompanied by gestures. For example, speakers tend to illustrate certain contents of speech by means of iconic gestures which are hand movements that bear a formal relationship to the contents of speech. The meaning of an iconic gesture is determined both by its form as well as the speech context in which it is performed. Thus, gesture and speech interact in comprehension. Using fMRI, the present study investigated what brain areas are involved in this interaction process. Participants watched videos in which sentences containing an ambiguous word (e.g. She touched the mouse) were accompanied by either a meaningless grooming movement, a gesture supporting the more frequent dominant meaning (e.g. animal) or a gesture supporting the less frequent subordinate meaning (e.g. computer device). We hypothesized that brain areas involved in the interaction of gesture and speech would show greater activation to gesture-supported sentences as compared to sentences accompanied by a meaningless grooming movement. The main results are that when contrasted with grooming, both types of gestures (dominant and subordinate) activated an array of brain regions consisting of the left posterior superior temporal sulcus (STS), the inferior parietal lobule bilaterally and the ventral precentral sulcus bilaterally. Given the crucial role of the STS in audiovisual integration processes, this activation might reflect the interaction between the meaning of gesture and the ambiguous sentence. The activations in inferior frontal and inferior parietal regions may reflect a mechanism of determining the goal of co-speech hand movements through an observation-execution matching process

Who is that? Brain networks and mechanisms for identifying individuals

Social animals can identify conspecifics by many forms of sensory input. However, whether the neuronal computations that support this ability to identify individuals rely on modality-independent convergence or involve ongoing synergistic interactions along the multiple sensory streams remains controversial. Direct neuronal measurements at relevant brain sites could address such questions, but this requires better bridging the work in humans and animal models. Here, we overview recent studies in nonhuman primates on voice and face identity-sensitive pathways and evaluate the correspondences to relevant findings in humans. This synthesis provides insights into converging sensory streams in the primate anterior temporal lobe (ATL) for identity processing. Furthermore, we advance a model and suggest how alternative neuronal mechanisms could be tested

The social brain: neural basis of social knowledge

Social cognition in humans is distinguished by psychological processes that allow us to make inferences about what is going on inside other people—their intentions, feelings, and thoughts. Some of these processes likely account for aspects of human social behavior that are unique, such as our culture and civilization. Most schemes divide social information processing into those processes that are relatively automatic and driven by the stimuli, versus those that are more deliberative and controlled, and sensitive to context and strategy. These distinctions are reflected in the neural structures that underlie social cognition, where there is a recent wealth of data primarily from functional neuroimaging. Here I provide a broad survey of the key abilities, processes, and ways in which to relate these to data from cognitive neuroscience

A core eating network and its modulations underlie diverse eating phenomena

We propose that a core eating network and its modulations account for much of what is currently known about the neural activity underlying a wide range of eating phenomena in humans (excluding homeostasis and related phenomena). The core eating network is closely adapted from a network that Kaye, Fudge, and Paulus (2009) proposed to explain the neurocircuitry of eating, including a ventral reward pathway and a dorsal control pathway. In a review across multiple literatures that focuses on experiments using functional Magnetic Resonance Imaging (fMRI), we first show that neural responses to food cues, such as food pictures, utilize the same core eating network as eating. Consistent with the theoretical perspective of grounded cognition, food cues activate eating simulations that produce reward predictions about a perceived food and potentially motivate its consumption. Reviewing additional literatures, we then illustrate how various factors modulate the core eating network, increasing and/or decreasing activity in subsets of its neural areas. These modulating factors include food significance (palatability, hunger), body mass index (BMI, overweight/obesity), eating disorders (anorexia nervosa, bulimia nervosa, binge eating), and various eating goals (losing weight, hedonic pleasure, healthy living). By viewing all these phenomena as modulating a core eating network, it becomes possible to understand how they are related to one another within this common theoretical framework. Finally, we discuss future directions for better establishing the core eating network, its modulations, and their implications for behavior

Neural Correlates of Repetition Priming: Changes in fMRI Activation and Synchrony

The neural mechanisms of behavioural priming remain unclear. Recent studies have suggested that category-preferential regions in ventral occipitotemporal cortex (VOTC) play an important role; some have reported increased neural synchrony between prefrontal cortex and temporal cortex associated with stimulus repetition. Based on these results, I hypothesized that increased neural synchrony, as measured by functional connectivity analysis using functional MRI, between category-preferential regions in VOTC and broader category-related networks would underlie behavioural priming. To test this hypothesis, I localized several category-preferential regions in VOTC using an independent functional localizer. Then, Seed Partial Least Squares was used to assess task-related functional connectivity of these regions across repetition of stimuli from multiple categories during an independent semantic classification task. While the results did not show the hypothesized differences in functional connectivity across stimulus repetition, evidence of category-specificity of neural priming and novel insights about the nature of category-related organization of VOTC were revealed

DEVELOPMENTAL FMRI STUDY: FACE AND OBJECT RECOGNITION

Visual processing, though seemingly automatic, is complex. Typical humansprocess objects and faces routinely. Yet, when a disease or disorder disrupts face andobject recognition, the effects are profound. Because of its importance and complexity,visual processing has been the subject of many adult functional imaging studies.However, relatively little is known about the development of the neural organization andunderlying cognitive mechanisms of face and object recognition. The current projectused functional magnetic resonance imaging (fMRI) to identify maturational changes inthe neural substrates of face and object recognition in 5-8 year olds, 9-11 year olds, andadults. A passive face and object viewing task revealed cortical shifts in the faceresponsiveloci of the ventral processing stream (VPS), an inferior occipito-temporalregion known to function in higher visual processing. Older children and adults recruitedmore anterior regions of the ventral processing stream than younger children. Toinvestigate the potential cognitive basis for these developmental changes, researchersimplemented a shape-matching task with parametric variations of shape overlap,structural similarity (SS), in stimulus pairs. VPS regions sensitive to high SS emerged inolder children and adults. Younger children recruited no structurally-sensitive regions inthe VPS. Two right hemisphere VPS regions were sensitive to maturational changes inSS. A comparison of face-responsive regions from the passive viewing task and the VPSSS regions did not reveal overlap. Though SS drives organization of the VPS, it did notexplain the cortical shifts in the neural substrates for face processing. In addition to VPSregions, results indicated additional maturational SS changes in frontal, parietal, andcerebellar regions. Based on these findings, further analyses were conducted to quantifyand qualify maturational changes in face and object processing throughout the brain.Results indicated developmental changes in activation extent, signal magnitude, andlateralization of face and object recognition networks. Collectively, this project supportsa developmental change in visual processing between 5-8 years and 9-11 years of age.Chapters Four through Six provide an in-depth discussion of the implications of thesefindings

Functional organisation of anterior thoracic stretch receptors in the deep-sea isopod Bathynomus doederleini: Behavioural, morphological and physiological studies

The relationship between segmental mobility and the organisation of thoracic stretch receptors was examined in the deep-sea isopod Bathynomus doederleini, which shows a developed adaptive behaviour during digging. The movements of segments during digging were analysed from video recordings, which showed that a large excursion occurred in the anterior thoracic segments. Dyefills of axons revealed four types of thoracic stretch receptor (TSR): an N-cell type (TSR-1), a differentiated Ncell type (TSR-2), a muscle receptor organ (MRO)-type with a long, single receptor muscle (TSR-3) and an MROtype with a short, single receptor muscle (TSR-4 to TSR-7). Physiologically, TSR-1 and TSR-2 are tonic-type stretch receptors. TSR-3 to TSR-7 show two kinds of stretchactivated responses, a tonic response and a phasico-tonic response in which responses are maintained as long as the stretch stimulus is delivered. Both TSR-2, with a long muscle strand, and TSR-3, with a single, long receptor muscle, have a wide dynamic range in their stretchactivated response. In addition, TSR-2 is controlled by an intersegmental inhibitory reflex from TSR-3. These results suggest that, although TSR-1 has no receptor muscle and TSR-2 has a less-differentiated receptor-like muscle, they are fully functional position detectors of segmental movements, as are the MRO-type receptors TSR-3 to TSR-7.</p

Regional differences in the coupling between resting cerebral blood flow and metabolism may indicate action preparedness as a default state.

Although most functional neuroimaging studies examine task effects, interest intensifies in the "default" resting brain. Resting conditions show consistent regional activity, yet oxygen extraction fraction constancy across regions. We compared resting cerebral metabolic rates of glucose (CMRgl) measured with 18F-labeled 2-fluoro-2-deoxy-D-glucose to cerebral blood flow (CBF) 15O-H2O measures, using the same positron emission tomography scanner in 2 samples (n = 60 and 30) of healthy right-handed adults. Region to whole-brain ratios were calculated for 35 standard regions of interest, and compared between CBF and CMRgl to determine perfusion relative to metabolism. Primary visual and auditory areas showed coupling between CBF and CMRgl, limbic and subcortical regions--basal ganglia, thalamus and posterior fossa structures--were hyperperfused, whereas association cortices were hypoperfused. Hyperperfusion was higher in left than right hemisphere for most cortical and subcallosal limbic regions, but symmetric in cingulate, basal ganglia and somatomotor regions. Hyperperfused regions are perhaps those where activation is anticipated at short notice, whereas downstream cortical modulatory regions have longer "lead times" for deployment. The novel observation of systematic uncoupling of CBF and CMRgl may help elucidate the potential biological significance of the "default" resting state. Whether greater left hemispheric hyperperfusion reflects lateral dominance needs further examination