Responses to lightness variations in early human visual cortex

Lightness is the apparent reflectance of a surface, and it depends not only on the actual luminance of the surface but also on the context in which the surface is viewed [1-10]. The cortical mechanisms of lightness processing are largely unknown, and the role of early cortical areas is still a matter of debate [11-17]. We studied the cortical responses to lightness variations in early stages of the human visual system with functional magnetic resonance imaging (fMRI) while observers were performing a demanding fixation task. The set of dynamically presented visual stimuli included the rectangular version of the classic Craik-O'Brien stimulus [3, 18, 19] and a variant that led to a weaker lightness effect, as well as a pattern with actual luminance variations. We found that the cortical activity in retinotopic areas, including the primary visual cortex (V1), is correlated with context-dependent lightness variations.     

A neural model of surface perception: lightness, anchoring, and filling-in

A neural model is proposed of how the visual system processes natural images under variable illumination conditions to generate surface lightness percepts. Previous models clarify how the brain can compute relative contrast. The anchored Filling-In Lightness Model (aFILM) clarifies how the brain 'anchors' lightness percepts to determine an absolute lightness scale that uses the full dynamic range of neurons. The model quantitatively simulates lightness anchoring properties (Articulation, Insulation, Configuration, Area Effect) and other lightness data (discounting the illuminant, the double brilliant illusion, lightness constancy and contrast, Mondrian contrast constancy, Craik-O'Brien-Cornsweet illusion). The model clarifies how retinal processing stages achieve light adaptation and spatial contrast adaptation, and how cortical processing stages fill-in surface lightness using long-range horizontal connections that are gated by boundary signals. The new filling-in mechanism runs 1000 times faster than diffusion mechanisms of previous filling-in models.     

Colors of night: climate–morphology relationships of geometrid moths along spatial gradients in southwestern China

Oecologia - Color lightness of insects is an important ecological trait affecting their performance through multiple functions such as thermoregulation, UV protection and disease resistance. The...     

Effect of pictorial depth cues, binocular disparity cues and motion parallax depth cues on lightness perception in three-dimensional virtual scenes

Background

Surface lightness perception is affected by scene interpretation. There is some experimental evidence that perceived lightness under bi-ocular viewing conditions is different from perceived lightness in actual scenes but there are also reports that viewing conditions have little or no effect on perceived color. We investigated how mixes of depth cues affect perception of lightness in three-dimensional rendered scenes containing strong gradients of illumination in depth.

Methodology/Principal Findings

Observers viewed a virtual room (4 m width×5 m height×17.5 m depth) with checkerboard walls and floor. In four conditions, the room was presented with or without binocular disparity (BD) depth cues and with or without motion parallax (MP) depth cues. In all conditions, observers were asked to adjust the luminance of a comparison surface to match the lightness of test surfaces placed at seven different depths (8.5–17.5 m) in the scene. We estimated lightness versus depth profiles in all four depth cue conditions. Even when observers had only pictorial depth cues (no MP, no BD), they partially but significantly discounted the illumination gradient in judging lightness. Adding either MP or BD led to significantly greater discounting and both cues together produced the greatest discounting. The effects of MP and BD were approximately additive. BD had greater influence at near distances than far.

Conclusions/Significance

These results suggest the surface lightness perception is modulated by three-dimensional perception/interpretation using pictorial, binocular-disparity, and motion-parallax cues additively. We propose a two-stage (2D and 3D) processing model for lightness perception.     

Selection of visual information for lightness judgements by eye movements

When judging the lightness of objects, the visual system has to take into account many factors such as shading, scene geometry, occlusions or transparency. The problem then is to estimate global lightness based on a number of local samples that differ in luminance. Here, we show that eye fixations play a prominent role in this selection process. We explored a special case of transparency for which the visual system separates surface reflectance from interfering conditions to generate a layered image representation. Eye movements were recorded while the observers matched the lightness of the layered stimulus. We found that observers did focus their fixations on the target layer, and this sampling strategy affected their lightness perception. The effect of image segmentation on perceived lightness was highly correlated with the fixation strategy and was strongly affected when we manipulated it using a gaze-contingent display. Finally, we disrupted the segmentation process showing that it causally drives the selection strategy. Selection through eye fixations can so serve as a simple heuristic to estimate the target reflectance.     

Lightness, illumination, and gradients

The illumination interpretation approach claims that lightness illusions can be explained as misapplications of lightness constancy mechanisms, processes which usually enable veridical extraction of surface reflectance from luminance distributions by discounting illumination. In particular, luminance gradients are thought to provide cues about the interactions of light and surfaces. Several examples of strong lightness illusions are discussed for which explanations based on illumination interpretation can be proposed. In criticisms of this approach, a variety of demonstrations of similarly structured control displays are presented, which involve equivalent lightness effects that cannot readily be accounted for by illumination interpretation mechanisms. Furthermore, a number of known and novel displays are presented that demonstrate effects of gradients on the qualitative appearance of uniform regions. Finally, some simple simulations of neural effects of luminance distributions are discussed.     

基于计算机视觉的罗非鱼适应环境的体色变化研究

多数鱼类的体色会受应激条件、环境背景、健康状况、生长发育和社会地位等因素的影响而发生改变。本文利用基于计算机视觉的体色量化技术研究正常情况和社会应激条件下罗非鱼对背景颜色的适应性,以及在背景颜色变化过程中体色变化的响应速度。实验结果表明：已适应白色背景的鱼放入黑色背景水体后,体色变化主要发生在前10s内,放入时和放入10s后的体色明度值差异极显著（**p＜0.01）;在白色背景下适应的鱼放入黑色背景下适应2h后其体色变得很黑,将其放入白色背景水体后体色在10s内可发生由深到浅的变化,放入时和放入10s后的体色明度值差异极显著（** p＜0.01）。在蓝色背景下适应的鱼放入黑色背景水体后,体色变化主要发生在前10s内,放入时和放入10s后的体色明度值差异显著（*p＜0.05）。在蓝色背景下适应的鱼放入黑色背景下适应2h后的体色变得很黑,再将其放入白色背景水体后体色由深变浅,放入时和10s后的体色明度值发生极显著变化（**p＜0.01）。处于社会应激条件下劣势地位的鱼体色会变黑,刚放入白色背景水体时的平均灰级达到12.7阶,放入60s、1800s后的体色和刚放入时没有显著差异。受社会应激影响轻微的鱼体色在1800s后适应了环境的颜色,明度值和没有受应激影响鱼的体色接近,而受伤或受社会应激影响较严重的鱼体色改变较小。鱼在高浓度非离子氨（UIA浓度为0.178 mg/L）的水中处理3h后,鱼的体色变得很黑,刚放入白色背景水体时平均灰级达到15.1阶,放入10s、120s后鱼的体色变化不大,放入180s后鱼的体色变浅,平均灰级达到9.3阶,与刚放入时的体色明度相比差异显著（*p＜0.05）。     

Colour lightness of dragonfly assemblages across North America and Europe

Dark‐coloured ectotherms absorb energy from the environment at higher rates than light‐coloured ectotherms. The thermal melanism hypothesis (TMH) states that this physical mechanism links the colour lightness of the body surfaces of ectotherms to their thermal environment and hence to their geographical distribution. Studies on different insect taxa in Europe found support for this prediction of the TMH. However, whether these results hold also for other biogeographical regions remains unclear. Here, we quantify and map the colour lightness of dragonfly species in North America and directly compare our results to previously published findings for Europe. We estimated the colour lightness of 152 North American dragonfly species from published illustrations, compiled their distribution data from the literature and combined all these data with six biologically relevant environmental variables. We evaluated the importance of phylogenetic autocorrelation for the spatial variation of mean colour lightness of dragonfly assemblages (grid cells of approximately 50 × 50 km size) by repeating all analyses also for the phylogenetically predicted component of the colour lightness of species and the species‐specific deviation from this prediction. We also accounted for spatial autocorrelation with autoregressive error models. All statistical approaches showed that dragonfly assemblages from both continents consistently tended to be darker coloured in regions with cold climates and lighter coloured in regions with warm climates. Regression slopes, however, were significantly less steep, and the amount of variance explained by environmental variables was lower for North America than for Europe. Our results highlight the importance of colour lightness for the distribution of dragonfly species, but they also indicate that idiosyncrasies of the continents modify the general pattern.     

Does luminance contrast determine lightness?

When presented against a highly lit black background, dimly illuminated white paper strips appear white even when they are equiluminant with the background. Such an example of simultaneous lightness constancy cannot be accounted for by receptor gain control because of the equiluminance. Moreover, this demonstration shows that lightness cannot be reduced to 'relative brightness' as is widely believed.     

The dynamic range of human lightness perception

Natural viewing challenges the visual system with images that have a dynamic range of light intensity (luminance) that can approach 1,000,000:1 and that often exceeds 10,000:1 [1, 2]. The range of perceived surface reflectance (lightness), however, can be well approximated by the Munsell matte neutral scale (N 2.0/ to N 9.5/), consisting of surfaces whose reflectance varies by about 30:1. Thus, the visual system must map a large range of surface luminance onto a much smaller range of surface lightness. We measured this mapping in images with a dynamic range close to that of natural images. We studied simple images that lacked segmentation cues that would indicate multiple regions of illumination. We found a remarkable degree of compression: at a single image location, a stimulus luminance range of 5,905:1 can be mapped onto an extended lightness scale that has a reflectance range of 100:1. We characterized how the luminance-to-lightness mapping changes with stimulus context. Our data rule out theories that predict perceived lightness from luminance ratios or Weber contrast. A mechanistic model connects our data to theories of adaptation and provides insight about how the underlying visual response varies with context.     

On-line evaluation of fermentation broth colour

Summary A novel method for evaluating pigment production during fermentation ofMonascus ruber has been developed and consists of reflectance measurement with a 10° observer under an artificial illuminant. A spectrophotometer was adapted to measure pigmentation during culture in a bioreactor. The lightness parameter L was the most useful information delivered by this sensor. An absorbency over 30 units at 480nm on batch cultures was estimated on-line without dilution. member of the GR Automatique - SARTA - CNRS     

Color and lightness constancy in different perceptual tasks

Color and lightness constancy with respect to changing illumination was studied with three different perceptual tasks: ranking of colored papers according (1) to their lightness and (2) to their chromatic similarity in photopic, mesopic, and scotopic states of adaptation, and (3) recognition of remembered colored papers after changes of illumination in photopic vision. Constancy was found in the second task, only. Excitations of light receptors and luminance channels were computed to simulate the empirical rank orders. Results of the first task can be predicted with the hypothesis that luminance channels are activated, if lightness is asked for. Sequences arranged with respect to chromatic similarity were found independent of the illuminant spectra, even if the calculated rank orders of cone excitation were changed in the altered illumination. Received: 4 October 1997 / Accepted in revised form: 26 August 1998     

Adelson's tile and snake illusions: a Helmholtzian type of simultaneous lightness contrast

Adelson's tile, snake, and some other lightness illusions of the same type were measured with the Munsell neutral scale for twenty observers. It was shown that theories based on low-level luminance contrast processing could hardly explain these illusions. Neither can those based on luminance X-junctions. On the other hand, Helmholtz's idea, that simultaneous lightness contrast originates from an error in judgement of apparent illumination, has been elaborated so as to account for the tile and snake illusions as well as other demonstrations presented in this report.     

Temperature‐driven color lightness and body size variation scale to local assemblages of European Odonata but are modified by propensity for dispersal

1. Previous macrophysiological studies suggested that temperature‐driven color lightness and body size variations strongly influence biogeographical patterns in ectotherms. However, these trait–environment relationships scale to local assemblages and the extent to which they can be modified by dispersal remains largely unexplored. We test whether the predictions of the thermal melanism hypothesis and the Bergmann's rule hold for local assemblages. We also assess whether these trait–environment relationships are more important for species adapted to less stable (lentic) habitats, due to their greater dispersal propensity compared to those adapted to stable (lotic) habitats.
2. We quantified the color lightness and body volume of 99 European dragon‐ and damselflies (Odonata) and combined these trait information with survey data for 518 local assemblages across Europe. Based on this continent‐wide yet spatially explicit dataset, we tested for effects temperature and precipitation on the color lightness and body volume of local assemblages and assessed differences in their relative importance and strength between lentic and lotic assemblages, while accounting for spatial and phylogenetic autocorrelation.
3. The color lightness of assemblages of odonates increased, and body size decreased with increasing temperature. Trait–environment relationships in the average and phylogenetic predicted component were equally important for assemblages of both habitat types but were stronger in lentic assemblages when accounting for phylogenetic autocorrelation.
4. Our results show that the mechanism underlying color lightness and body size variations scale to local assemblages, indicating their general importance. These mechanisms were of equal evolutionary significance for lentic and lotic species, but higher dispersal ability seems to enable lentic species to cope better with historical climatic changes. The documented differences between lentic and lotic assemblages also highlight the importance of integrating interactions of thermal adaptations with proxies of the dispersal ability of species into trait‐based models, for improving our understanding of climate‐driven biological responses.

     

SNP-Based Genetic Linkage Map and Quantitative Trait Locus Mapping Associated with the Agronomically Important Traits of Hypsizygus marmoreus

White strains of Hypsizygus marmoreus are more difficult to cultivate than are brown strains; therefore, new white strain breeding strategies are required. Accordingly, we constructed the genetic map of H. marmoreus with 1996 SNP markers on 11 linkage groups (LGs) spanning 1380.49 cM. Prior to analysis, 82 backcrossed strains (HM8 lines) were generated by mating between KMCC03106-31 and the progenies of the F₁ hybrid (Hami-18 × KMCC03106-93). Using HM8, the first 23 quantitative trait loci (QTLs) of yield-related traits were detected with high limit of detection (LOD) scores (1.98–9.86). The length, thickness, and hardness of the stipe were colocated on LG 1. Especially, length of stipe and thickness of stipe were highly correlated given that the correlation coefficients were negative (−0.39, p value ≤ .01). And a typical biomodal distribution was observed for lightness of the pileus and the lightness of the pileus trait belonged to the LG 8, as did traits of earliness and mycelial growth in potato dextrose agar (PDA) medium. Therefore, results for color traits can be suggested that color is controlled by a multi-gene of one locus. The yield trait was highly negatively correlated with the traits for thickness of the stipe (−0.45, p value ≤ .01). Based on additive effects, the white strain was confirmed as recessive; however, traits of mycelial growth, lightness, and quality were inherited by backcrossed HM8 lines. This new genetic map, finely mapped QTLs, and the strong selection markers could be used in molecular breeding of H. marmoreus.     

Habitat structure and prey composition generate contrasting effects on carotenoid‐based coloration of great tit Parus major nestlings

Carotenoid‐based coloration of nestling plumage is generally considered a reliable signal of quality and has consistently been related to habitat structure. The main hypothesis proposed to explain this correlation is that high quality habitats contain high quality food, which in return affects the expression of carotenoid‐based plumage. It therefore assumes that, at the population level, the link between habitat structure and food composition is consistent and more relevant than inter‐individual differences in foraging ability or parental investment. In addition, it is assumed by default that food and habitat produce concordant effects on nestling coloration. In this work we evaluated habitat structure and prey composition in addition to several measures of parental investment. We investigated their relative effect on carotenoid‐based plumage coloration (lightness, chroma and hue) of great tit Parus major nestlings. We found a low correlation between carotenoid‐based coloration of nestlings and that of their parents. Nestling coloration, especially lightness and chroma, increased with the intake of more spiders. The time of breeding was positively correlated with lightness and chroma and negatively correlated with hue. Finally, the maturity of oak trees surrounding nest‐boxes correlated negatively with lightness, and the size of all tree species surrounding nest‐boxes correlated positively with hue of chick plumage. Our findings support the view that habitat structure and prey composition may produce divergent effects on feather pigmentation, and that prey proportions and variables related to parental investment should be assessed when considering carotenoid‐based coloration of chicks. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 113 , 547–555.     

Visual neuroscience: illuminating the dark corners

Recent experiments suggest that our perception of lightness involves a sophisticated interpretation of illumination and shadow. This finding challenges common notions about hierarchical processing and the neural basis of perception.     

Reinterpreting Behavioral Receptive Fields: Lightness Induction Alters Visually Completed Shape

Background

A classification image (CI) technique has shown that static luminance noise near visually completed contours affects the discrimination of fat and thin Kanizsa shapes. These influential noise regions were proposed to reveal “behavioral receptive fields” of completed contours–the same regions to which early cortical cells respond in neurophysiological studies of contour completion. Here, we hypothesized that 1) influential noise regions correspond to the surfaces that distinguish fat and thin shapes (hereafter, key regions); and 2) key region noise biases a “fat” response to the extent that its contrast polarity (lighter or darker than background) matches the shape''s filled-in surface color.

Results

To test our hypothesis, we had observers discriminate fat and thin noise-embedded rectangles that were defined by either illusory or luminance-defined contours (Experiment 1). Surrounding elements (“inducers”) caused the shapes to appear either lighter or darker than the background–a process sometimes referred to as lightness induction. For both illusory and luminance-defined rectangles, key region noise biased a fat response to the extent that its contrast polarity (light or dark) matched the induced surface color. When lightness induction was minimized, luminance noise had no consistent influence on shape discrimination. This pattern arose when pixels immediately adjacent to the discriminated boundaries were excluded from the analysis (Experiment 2) and also when the noise was restricted to the key regions so that the noise never overlapped with the physically visible edges (Experiment 3). The lightness effects did not occur in the absence of enclosing boundaries (Experiment 4).

Conclusions

Under noisy conditions, lightness induction alters visually completed shape. Moreover, behavioral receptive fields derived in CI studies do not correspond to contours per se but to filled-in surface regions contained by those contours. The relevance of lightness to two-dimensional shape completion supplies a new constraint for models of object perception.     

Adaptation of Pelage Color and Pigment Variations in Israeli Subterranean Blind Mole Rats,Spalax Ehrenbergi

Background

Concealing coloration in rodents is well established. However, only a few studies examined how soil color, pelage color, hair-melanin content, and genetics (i.e., the causal chain) synergize to configure it. This study investigates the causal chain of dorsal coloration in Israeli subterranean blind mole rats, Spalax ehrenbergi.

Methods

We examined pelage coloration of 128 adult animals from 11 populations belonging to four species of Spalax ehrenbergi superspecies (Spalax galili, Spalax golani, Spalax carmeli, and Spalax judaei) and the corresponding coloration of soil samples from the collection sites using a digital colorimeter. Additionally, we quantified hair-melanin contents of 67 animals using HPLC and sequenced the MC1R gene in 68 individuals from all four mole rat species.

Results

Due to high variability of soil colors, the correlation between soil and pelage color coordinates was weak and significant only between soil hue and pelage lightness. Multiple stepwise forward regression revealed that soil lightness was significantly associated with all pelage color variables. Pelage color lightness among the four species increased with the higher southward aridity in accordance to Gloger''s rule (darker in humid habitats and lighter in arid habitats). Darker and lighter pelage colors are associated with darker basalt and terra rossa, and lighter rendzina soils, respectively. Despite soil lightness varying significantly, pelage lightness and eumelanin converged among populations living in similar soil types. Partial sequencing of the MC1R gene identified three allelic variants, two of which were predominant in northern species (S. galili and S. golani), and the third was exclusive to southern species (S. carmeli and S. judaei), which might have caused the differences found in pheomelanin/eumelanin ratio.

Conclusion/Significance

Darker dorsal pelage in darker basalt and terra rossa soils in the north and lighter pelage in rendzina and loess soils in the south reflect the combined results of crypsis and thermoregulatory function following Gloger''s rule.     

百日草链格孢菌粗毒素的生产、提取及稳定性的研究

百日草链格孢菌是从世界性恶性杂草苍耳罹病植株上分离得到的植物病原真菌,研究表明该菌对紫茎泽兰有致病作用,可产生致病的次生代谢产物--毒素。本文对该菌的次生代谢产毒能力情况进行了研究。对培养基条件进行了筛选,确定了有利于该菌产毒的温度为25℃、pH值为6.5、培养时间为9～12天、足够的黑暗以及溶氧、转速等培养条件。利用大规模发酵与发酵产物后提取工艺获取粗毒素并通过分析贮存时间、温度、光照对粗毒素稳定性的影响表明具有开发天然微生物源除草剂的潜力。