Co-Planar Stereotaxic Atlas of the Human Brain—3-Dimensional Proportional System: An Approach to Cerebral Imaging, J. Talairach, P. Tournoux. Georg Thieme Verlag, New York (1988), 122 pp., 130 figs. DM 268

Behavioral scientists routinely publish broad claims about human psychology and behavior in the world's top journals based on samples drawn entirely from Western, Educated, Industrialized, Rich, and Democratic (WEIRD) societies. Researchers - often implicitly - assume that either there is little variation across human populations, or that these "standard subjects" are as representative of the species as any other population. Are these assumptions justified? Here, our review of the comparative database from across the behavioral sciences suggests both that there is substantial variability in experimental results across populations and that WEIRD subjects are particularly unusual compared with the rest of the species - frequent outliers. The domains reviewed include visual perception, fairness, cooperation, spatial reasoning, categorization and inferential induction, moral reasoning, reasoning styles, self-concepts and related motivations, and the heritability of IQ. The findings suggest that members of WEIRD societies, including young children, are among the least representative populations one could find for generalizing about humans. Many of these findings involve domains that are associated with fundamental aspects of psychology, motivation, and behavior - hence, there are no obvious a priori grounds for claiming that a particular behavioral phenomenon is universal based on sampling from a single subpopulation. Overall, these empirical patterns suggests that we need to be less cavalier in addressing questions of human nature on the basis of data drawn from this particularly thin, and rather unusual, slice of humanity. We close by proposing ways to structurally re-organize the behavioral sciences to best tackle these challenges.

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The WEIRDest People in the World

1. Introduction and Overview. 2. Detecting Influential Observations and Outliers. 3. Detecting and Assessing Collinearity. 4. Applications and Remedies. 5. Research Issues and Directions for Extensions. Bibliography. Author Index. Subject Index.

Regression Diagnostics: Identifying Influential Data and Sources of Collinearity

The dementia with Lewy bodies (DLB) Consortium has revised criteria for the clinical and pathologic diagnosis of DLB incorporating new information about the core clinical features and suggesting improved methods to assess them. REM sleep behavior disorder, severe neuroleptic sensitivity, and reduced striatal dopamine transporter activity on functional neuroimaging are given greater diagnostic weighting as features suggestive of a DLB diagnosis. The 1-year rule distinguishing between DLB and Parkinson disease with dementia may be difficult to apply in clinical settings and in such cases the term most appropriate to each individual patient should be used. Generic terms such as Lewy body (LB) disease are often helpful. The authors propose a new scheme for the pathologic assessment of LBs and Lewy neurites (LN) using alpha-synuclein immunohistochemistry and semiquantitative grading of lesion density, with the pattern of regional involvement being more important than total LB count. The new criteria take into account both Lewy-related and Alzheimer disease (AD)-type pathology to allocate a probability that these are associated with the clinical DLB syndrome. Finally, the authors suggest patient management guidelines including the need for accurate diagnosis, a target symptom approach, and use of appropriate outcome measures. There is limited evidence about specific interventions but available data suggest only a partial response of motor symptoms to levodopa: severe sensitivity to typical and atypical antipsychotics in ∼50%, and improvements in attention, visual hallucinations, and sleep disorders with cholinesterase inhibitors.

Diagnosis and management of dementia with Lewy bodies: Third report of the DLB Consortium

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WEIRD languages have misled us, too [Comment on Henrich et al.]

1. To analyze the selectivity and the sparseness of firing to visual stimuli of single neurons in the primate temporal cortical visual area, neuronal responses were measured to a set of 68 visual stimuli in macaques performing a visual fixation task. The population of neurons analyzed had responses that occurred primarily to faces. The stimuli included 23 faces, and 45 nonface images of real-world scenes, so that the function of this brain region could be analyzed when it was processing natural scenes. 2. The neurons were selected to meet the previously used criteria of face selectivity by responding more than twice as much to the optimal face as to the optimal nonface stimulus in the set. Application of information theoretic analyses to the responses of these neurons confirmed that their responses contained much more information about which of 20 face stimuli had been seen (on average 0.4 bits) than about which (of 20) nonface stimuli had been seen (on average 0.07 bits). 3. The sparseness of the representation of a scene or object provided by each of these neurons (which can be thought of as the proportion of stimuli to which the neuron responds, and which is fundamental to understanding the network operation of the system) can be defined as [formula: see text] where ri is the firing rate to the ith stimulus in the set of n stimuli. The sparseness has a maximal value of 1.0. It was found that the sparseness of the representation of the 68 stimuli by each neuron had an average across all neurons of 0.65. This indicates a rather distributed representation. 4. If the spontaneous firing rate was subtracted from the firing rate of the neuron to each stimulus, so that the changes of firing rate, i.e., the responses of the neurons, were used in the sparseness calculation, then the "response sparseness" had a lower value, with a mean of 0.33 for the population of neurons, or 0.60 if calculated over the set of faces. 5. Multidimensional scaling to produce a stimulus space represented by this population of neurons showed that the different faces were well separated in the space created, whereas the different nonface stimuli were grouped together in the space. 6. The information analyses and multidimensional scaling provided evidence that what was made explicit in the responses of these neurons was information about which face had been seen.(ABSTRACT TRUNCATED AT 400 WORDS)

https://www.oxcns.org/papers/196_Rolls+Tovee95.pdf

Sparseness of the neuronal representation of stimuli in the primate temporal visual cortex

In experiments to investigate the duration of the time for which cortical neurons respond when the identification of a visual stimulus is just possible, we presented a test face stimulus for 16 ms, and followed it at different intervals by a masking stimulus (either an N-O pattern or a face) while recording from single neurons in the temporal visual cortex of macaques. When there was no mask the cells responded to the 16 ms of the test stimulus for 200-300 ms, far longer than the presentation time. We suggest that this reflects the operation of a short-term memory system implemented in cortical circuitry. If the mask was a stimulus which did not stimulate the cells (either a non-face pattern or a face which was a non-effective stimulus for that cell), then, as the interval between the onset of the test stimulus and the onset of the mask stimulus (the stimulus onset asynchrony) was reduced, the length of time for which the cells fired in response to the test stimulus was reduced. It is suggested that this is due to the mask stimulating adjacent cells in the cortex which by lateral inhibition reduce the responses of the cells activated by the test stimulus. When the stimulus onset asynchrony was 20 ms, face-selective neurons in the inferior temporal cortex of macaques responded for a period of 20-30 ms before their firing was interrupted by the mask. With the same test-mask stimulus onset asynchrony of 20 ms, humans could just identify which of six faces was shown. These results provide evidence that a cortical area can perform its computation necessary for the recognition of a visual stimulus in 20-30 ms, and provide a fundamental constraint which must be accounted for in any theory of cortical computation.

Processing speed in the cerebral cortex and the neurophysiology of visual masking.

1. The possibility of temporal encoding in the spike trains of single neurons recorded in the temporal lobe visual cortical areas of rhesus macaques was analyzed with the use of principal component and information theory analyses of smoothed spike trains. The neurons analyzed had responses selective for faces. 2. Provided that a correction was applied to earlier methods of principal component analysis used for neuronal spike trains, it was shown that the first principal component provides by a great extent the most information, with the second and third adding only small proportions (on average 18.8 and 8.4%, respectively). 3. It was shown that the magnitude of the second and higher principal components is even smaller if the spike train analysis is started after the onset of the neuronal response, instead of before the neuronal response has started. This suggests that variations in response latency are at least a part of what is reflected by the second and higher principal components. 4. The first principal component was correlated with the mean firing rate of the neurons. The second and higher principal components reflected at least partly the onset properties of the neuronal responses, such as response latency differences between the stimuli. 5. A considerable proportion of the information available from principal components 1-3 is available in the firing rate of the neuron. 6. Periods of the firing rate of as little as 50 or even 20 ms are sufficient to give a reasonable estimate of the firing rate of the neuron. 7. Information theory analysis showed that in short epochs (e.g., 50 ms) the information available from the firing rate can be as high, on average, as 84.4% of that available from the firing rate calculated over 400 ms, and 52.0% of that available from principal components 1-3 in the 400-ms period. It was also found that 44.0% of the information calculated from the first three principal components is available in the firing rates calculated over epochs as short as 20 ms. 8. More information was available near the start of the neuronal response, and the information available from short epochs became less later in the neuronal response. 9. Taken together, these analyses provide evidence that a short period of firing taken close to the start of the neuronal response provides a reasonable proportion of the total information that would be available if a long period of neuronal firing (e.g., 400 ms) were utilized to extract it, even if temporal encoding were used.(ABSTRACT TRUNCATED AT 400 WORDS)

https://www.oxcns.org/papers/172_Tovee+Rolls++93%20Information%20Encoding%20in%20IT.pdf

Information encoding and the responses of single neurons in the primate temporal visual cortex

https://isiarticles.com/bundles/Article/pre/pdf/35765.pdf

Male physical attractiveness in Britain and Malaysia: A cross-cultural study

Evolutionary psychology suggests that a woman's sexual attractiveness is based on cues of health and reproductive potential. In recent years, research has focused on the ratio of the width of the waist to the width of the hips (the waist-to-hip ratio (WHR). A low WHR (i.e. a curvaceous body) is believed to correspond to the optimal fat distribution for high fertility, and so this shape should be highly attractive. In this paper we present evidence that weight scaled for height (the body mass index (BMI)) is the primary determinant of sexual attractiveness rather than WHR. BMI is also strongly linked to health and reproductive potential. Furthermore, we show how covariation of apparent BMI and WHR in previous studies led to the overestimation of the importance of WHR in the perception of female attractiveness. Finally, we show how visual cues, such as the perimeter-area ratio (PAR), can provide an accurate and reliable index of an individual's BMI and could be used by an observer to differentiate between potential partners.

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Martin J. Tovée

Papers

Sparseness of the neuronal representation of stimuli in the primate temporal visual cortex

Processing speed in the cerebral cortex and the neurophysiology of visual masking.

Information encoding and the responses of single neurons in the primate temporal visual cortex

Male physical attractiveness in Britain and Malaysia: A cross-cultural study

Visual cues to female physical attractiveness.