Tetrachromacy: the mysterious case of extra-ordinary color vision

Recent years have witnessed a growing public interest in human tetrachromacy – the possibility that a subpopulation of women enjoy an extra dimension of color vision. Yet, by contrast, rigorous studies of this unusual phenotype are sparse. The aim here is to offer the reader a guide to the facts and myths regarding this potential‘superpower’ and to address the core methodological issues that need to be considered when investigating it

Discrete element models for grain breakage

International audienc

Multidimensional scaling reveals a color dimension unique to 'color-deficient' observers

Normal color vision depends on the relative rates at which photons are absorbed in three types of retinal cone:short-wave (S), middle-wave (M) and long-wave (L) cones, maximally sensitive near 430, 530 and 560nm, respectively. But 6% of men exhibit an X-linked variant form of color vision called deuteranomaly [1]. Their color vision is thought to depend on S cones and two forms of long-wave cone (L, L′) [2,3]. The two types of L cone contain photopigments that are maximally sensitive near 560nm, but their spectral sensitivities are different enough that the ratio of their activations gives a useful chromatic signal

A population study of binocular function.

As part of a genome-wide association study (GWAS) of perceptual traits in healthy adults, we measured stereo acuity, the duration of alternative percepts in binocular rivalry and the extent of dichoptic masking in 1060 participants. We present the distributions of the measures, the correlations between measures, and their relationships to other psychophysical traits. We report sex differences, and correlations with age, interpupillary distance, eye dominance, phorias, visual acuity and personality. The GWAS, using data from 988 participants, yielded one genetic association that passed a permutation test for significance: The variant rs1022907 in the gene VTI1A was associated with self-reported ability to see autostereograms. We list a number of other suggestive genetic associations (p<10(-5)).This work was supported by the Gatsby Charitable Foundation (GAT2903). J.B. was supported by a fellowship from Gonville and Caius College.This is the author accepted manuscript. The final version is available from Elsevier via http://dx.doi.org/10.1016/j.visres.2015.02.01

42. Sons and mothers: classification of colour-deficient and heterozygous subjects by counterphase modulation photometry

Abstract In the OSCAR test of Estkvez et al. (1983) red and green lights are modulated in counterphase and the subject is asked to adjust their relative depths of modulation so as to minimize nicker. In a population consisting of normal mothers and carriers of colour deficiency (classified by their sons&apos; performance on the Nagel anomaloscope), the OSCAR settings of the mothers were strongly correlated with those of their sons. Protan and deutan carriers formed discrete populations; and many individual carriers of protan deficiencies could be distinguished from normals with confidence. Protan and deutan sons were distinguished from each other with complete reliability, but some deutan sons, and most deutan carriers, fell within the distribution of normal settings

Psychotic experiences, working memory, and the developing brain: a multimodal neuroimaging study

Psychotic experiences (PEs) occur in the general population, especially in children and adolescents, and are associated with poor psychosocial outcomes, impaired cognition, and increased risk of transition to psychosis. It is unknown how the presence and persistence of PEs during early adulthood affects cognition and brain function. The current study assessed working memory as well as brain function and structure in 149 individuals, with and without PEs, drawn from a population cohort. Observer-rated PEs were classified as persistent or transient on the basis of longitudinal assessments. Working memory was assessed using the n-back task during fMRI. Dynamic causal modeling (DCM) was used to characterize frontoparietal network configuration and voxel-based morphometry was utilized to examine gray matter. Those with persistent, but not transient, PEs performed worse on the n-back task, compared with controls, yet showed no significant differences in regional brain activation or brain structure. DCM analyses revealed greater emphasis on frontal connectivity within a frontoparietal network in those with PEs compared with controls. We propose that these findings portray an altered configuration of working memory function in the brain, potentially indicative of an adaptive response to atypical development associated with the manifestation of PEs

Individual differences in human eye movements: An oculomotor signature?

Human eye movements are stereotyped and repeatable, but how specific to a normal individual are the quantitative properties of his or her eye movements? We recorded saccades, anti-saccades and smooth-pursuit eye movements in a sample of over 1000 healthy young adults. A randomly selected subsample (10%) of participants were re-tested on a second occasion after a median interval of 18.8 days, allowing us to estimate reliabilities. Each of several derived measures, including latencies, accuracies, velocities, and left-right asymmetries, proved to be very reliable. We give normative means and distributions for each measure and describe the pattern of correlations amongst them. We identify several measures that exhibit significant sex differences. The profile of our oculomotor measures for an individual constitutes a personal oculomotor signature that distinguishes that individual from most other members of the sample of 1000.This research was funded by the Gatsby Charitable Foundation (GAT2903). PTG was supported by the Cambridge Commonwealth and Overseas Trusts and the Overseas Research Students Awards Scheme, and JMB by a Research Fellowship at Gonville and Caius College, Cambridge