castleCSF - A contrast sensitivity function of color, area, spatiotemporal frequency, luminance and eccentricity.

The contrast sensitivity function (CSF) is a fundamental visual model explaining our ability to detect small contrast patterns. CSFs found many applications in engineering, where they can be used to optimize a design for perceptual limits. To serve such a purpose, CSFs must explain possibly a complete set of stimulus parameters, such as spatial and temporal frequency, luminance, and others. Although numerous contrast sensitivity measurements can be found in the literature, none fully explains the complete space of stimulus parameters. Therefore, in this work, we first collect and consolidate contrast sensitivity measurements from 18 studies, which explain the sensitivity variation across the parameters of interest. Then, we build an analytical contrast sensitivity model that explains the data from all those studies. The proposed castleCSF model explains the sensitivity as the function of spatial and temporal frequencies, an arbitrary contrast modulation direction in the color space, mean luminance, and chromaticity of the background, eccentricity, and stimulus area. The proposed model uses the same set of parameters to explain the data from 18 studies with an error of 3.59 dB. The consolidated contrast sensitivity data and the code for the model are publicly available at https://github.com/gfxdisp/castleCSF/.

Odors modulate color appearance.

Our brain constantly combines multisensory information from our surrounding environment. Odors for instance are often perceived with visual cues; these sensations interact to form our own subjective experience. This integration process can have a profound impact on the resulting experience and can alter our subjective reality. Crossmodal correspondences are the consistent associations between stimulus features in different sensory modalities. These correspondences are presumed to be bidirectional in nature and have been shown to influence our perception in a variety of different sensory modalities. Vision is dominant in our multisensory perception and can influence how we perceive information in our other senses, including olfaction. We explored the effect that different odors have on human color perception by presenting olfactory stimuli while asking observers to adjust a color patch to be devoid of hue (neutral gray task). We found a shift in the perceived neutral gray point to be biased toward warmer colors. Four out of five of our odors also trend toward their expected crossmodal correspondences. For instance, when asking observers to perform the neutral gray task while presenting the smell of cherry, the perceptually achromatic stimulus was biased toward a red-brown. Using an achromatic adjustment task, we were able to demonstrate a small but systematic effect of the presence of odors on human color perception.

Performance Comparison of Classical Methods and Neural Networks for Colour Correction.

Colour correction is the process of converting RAW RGB pixel values of digital cameras to a standard colour space such as CIE XYZ. A range of regression methods including linear, polynomial and root-polynomial least-squares have been deployed. However, in recent years, various neural network (NN) models have also started to appear in the literature as an alternative to classical methods. In the first part of this paper, a leading neural network approach is compared and contrasted with regression methods. We find that, although the neural network model supports improved colour correction compared with simple least-squares regression, it performs less well than the more advanced root-polynomial regression. Moreover, the relative improvement afforded by NNs, compared to linear least-squares, is diminished when the regression methods are adapted to minimise a perceptual colour error. Problematically, unlike linear and root-polynomial regressions, the NN approach is tied to a fixed exposure (and when exposure changes, the afforded colour correction can be quite poor). We explore two solutions that make NNs more exposure-invariant. First, we use data augmentation to train the NN for a range of typical exposures and second, we propose a new NN architecture which, by construction, is exposure-invariant. Finally, we look into how the performance of these algorithms is influenced when models are trained and tested on different datasets. As expected, the performance of all methods drops when tested with completely different datasets. However, we noticed that the regression methods still outperform the NNs in terms of colour correction, even though the relative performance of the regression methods does change based on the train and test datasets.

Physicochemical features partially explain olfactory crossmodal correspondences.

During the olfactory perception process, our olfactory receptors are thought to recognize specific chemical features. These features may contribute towards explaining our crossmodal perception. The physicochemical features of odors can be extracted using an array of gas sensors, also known as an electronic nose. The present study investigates the role that the physicochemical features of olfactory stimuli play in explaining the nature and origin of olfactory crossmodal correspondences, which is a consistently overlooked aspect of prior work. Here, we answer the question of whether the physicochemical features of odors contribute towards explaining olfactory crossmodal correspondences and by how much. We found a similarity of 49% between the perceptual and the physicochemical spaces of our odors. All of our explored crossmodal correspondences namely, the angularity of shapes, smoothness of textures, perceived pleasantness, pitch, and colors have significant predictors for various physicochemical features, including aspects of intensity and odor quality. While it is generally recognized that olfactory perception is strongly shaped by context, experience, and learning, our findings show that a link, albeit small (6-23%), exists between olfactory crossmodal correspondences and their underlying physicochemical features.

Advancements in the dominion of fate and transport of pharmaceuticals and personal care products in the environment-a bibliometric study.

The study on the fate and transport of Pharmaceuticals and Personal Care Products, PPCPs (FTP) in the environment, has received particular attention for over two decades. The PPCPs threaten ecology and human health even at low concentrations due to their synergistic effects and long-range transport. The research aims to provide an inclusive map of the scientific background of FTP research over the last 25 years, from 1996 to 2020, to identify the main characteristics, evolution, salient research themes, trends, and research hotspots in the field of interest. Bibliometric networks were synthesized and analyzed for 577 journal articles extracted from the Scopus database. Consequently, seven major themes of FTP research were identified as follows: (i) PPCPs category; (ii) hazardous effects; (iii) occurrence of PPCPs; (iv) PPCPs in organisms; (v) remediation; (vi) FTP-governing processes; and (vii) assessment in the environment. The themes gave an in-depth picture of the sources of PPCPs and their transport and fate processes in the environment, which originated from sewage treatment plants and transported further to sediment/soils/groundwater/oceans that act as the PPCPs' major sink. The article provided a rigorous analysis of the research landscape in the FTP study conducted during the specified years. The prominent research themes, content analysis, and research hotspots identified in the study may serve as the basis of real-time guidance to lead future research areas and a prior review for policymakers and practitioners.

Spatio-chromatic contrast sensitivity under mesopic and photopic light levels.

Contrast sensitivity functions (CSFs) characterize the sensitivity of the human visual system at different spatial scales, but little is known as to how contrast sensitivity for achromatic and chromatic stimuli changes from a mesopic to a highly photopic range reflecting outdoor illumination levels. The purpose of our study was to further characterize the CSF by measuring both achromatic and chromatic sensitivities for background luminance levels from 0.02 cd/m2 to 7,000 cd/m2. Stimuli consisted of Gabor patches of different spatial frequencies and angular sizes, varying from 0.125 to 6 cpd, which were displayed on a custom high dynamic range (HDR) display with luminance levels up to 15,000 cd/m2. Contrast sensitivity was measured in three directions in color space, an achromatic direction, an isoluminant "red-green" direction, and an S-cone isolating "yellow-violet" direction, selected to isolate the luminance, L/M-cone opponent, and S-cone opponent pathways, respectively, of the early postreceptoral processing stages. Within each session, observers were fully adapted to the fixed background luminance (0.02, 2, 20, 200, 2,000, or 7,000 cd/m2). Our main finding is that the background luminance has a differential effect on achromatic contrast sensitivity compared to chromatic contrast sensitivity. The achromatic contrast sensitivity increases with higher background luminance up to 200 cd/m2 and then shows a sharp decline when background luminance is increased further. In contrast, the chromatic sensitivity curves do not show a significant sensitivity drop at higher luminance levels. We present a computational luminance-dependent model that predicts the CSF for achromatic and chromatic stimuli of arbitrary size.

Zika Virus: Immune Evasion Mechanisms, Currently Available Therapeutic Regimens, and Vaccines.

The sudden emergence of infectious pathogens such as Zika virus (ZIKV) holds global health concerns. Recent dissemination of ZIKV from Pacific to Americas with an upsurge of congenital anomalies and Guillain Barre Syndrome (GBS) in adults has created an alarming situation. High-throughput studies are in progress to understand ZIKV's mode of pathogenesis and mechanism of immune escape, yet the pathogenesis remains obscure. Mainly ZIKV's envelope (E) protein and nonstructural proteins (mainly NS1 and NS5) manipulate host cell to support viral immune escape by modulation of the interferon pathway and complement antagonism. The development of direct therapeutics for ZIKV infection is required to overcome the rapidly evolving viral threat. Currently, the existing strategies for ZIKV treatment are only supportive. Although, there is no prophylactic or therapeutic vaccine presently available, however, recent efforts have brought up ZIKV vaccines into clinical trial phase 1. This review presents the highlights of recent advances in understanding immune evasion strategies adapted by ZIKV and existing therapies against the virus.