基于H分量旋转的色盲矫正方法

为提高色盲患者的色彩分辨力,提出一种基于H分量旋转的色盲矫正方法。在颜色的HSI空间,利用H分量的连续性和周期性特点,在保持S、I分量不变的情况下,通过旋转H分量得到矫正图像,该图像以降低低频颜色的分辨率来换取高频颜色的分辨率提高。实验表明：在色盲类型给定且图像颜色是给定色盲易混淆的情况下,对H分量旋转120度能得到色彩分辨效果很好的矫正图像。     

基于颜色名和OpponentSIFT特征的鳞翅目昆虫图像识别

【目的】本研究旨在探索使用先进的计算机视觉技术实现对昆虫图像的自动分类方法。【方法】通过预处理对采集的昆虫标本图像去除背景,获得昆虫图像的前景蒙板,并由蒙板确定的轮廓计算出前景图像的最小包围盒,剪切出由最小包围盒确定的前景有效区域,然后对剪切得到的图像进行特征提取。首先提取颜色名特征,把原来的RGB（Red-Green-Blue）图像的像素值映射到11种颜色名空间,其值表示RGB值属于该颜色名的概率,每个颜色名平面划分成3×3像素大小的网格,用每格的概率均值作为网格中心点的描述子,最后用空阈金字塔直方图统计的方式形成颜色名视觉词袋特征;其次提取OpponentSIFT(Opponent Scale Invariant Feature Transform)特征,首先把RGB图像变换到对立色空间,对该空间每通道提取SIFT特征,最后用空域池化和直方图统计方法形成OpponentSIFT视觉词袋。将两种词袋特征串接后得到该昆虫图像的特征向量。使用昆虫图像样本训练集提取到的特征向量训练SVM（Support Vector Machine）分类器,使用这些训练得到的分类器即可实现对鳞翅目昆虫的分类识别。【结果】该方法在包含10种576个样本的昆虫图像数据库中进行了测试,取得了100%的识别正确率。【结论】试验结果证明基于颜色名和OpponentSIFT特征可以有效实现对鳞翅目昆虫图像的识别。     

图形简单几何特征的分辨及其相关错觉的定量研究

本实验用定量的心理物理测量方法,研究了在亮度对比与等亮度颜色对比的条件下,受试者分辨图形简单几何特征的能力以及与这些图形特征有关的错觉效应（Ｚｏｅｌｌｎｅｒ错觉、Ｍｕｌｌｅｒ－Ｌｙｅｒ错觉、Ｐｏｎｚｏ错觉和Ｄｅｌｂｏｅｕｆ错觉）。实验结果表明：受试者在亮度对比与颜色对比的条件下对线段平行度,线段长度与图形面积的分辨能力相同,与这些几何特征有关的错觉幅度也没有显著差异。但是,在等亮度颜色对比条件下,     

猕猴在自由或限制条件下的视觉或听觉分辨学习

本工作观察了猕猴在自由或限制条件下学习视觉或听觉分辨的规律。在WGTA内动物对颜色分辨学习有很大的个体差异,主要表现为学习初期正确反应率在机率水平波动的持续时间的不同。猴在WGTA内完成亮暗、物体及图形分辨学习,以及在限制椅上完成颜色分辨学习也有类似情况。从同一只猴在WGTA内进行不同的视觉分辨任务的学习所得的结果表明,物体分辨和亮暗分辨学习比之颜色分辨学习要容易些,图形分辨学习则相对地比较困难。猴在限制椅上学习颜色分辨比在WGTA内需要更多的测试数。动物在限制椅上学习纯音音调分辨似乎更为困难。这些结果对神经精神药理学、心理生理学以及神经生理学研究中选择合适的动物实验模型有一定的参考价值。     

朝向和对比度同时快速变化条件下的分辨能力

在自然的视觉中,投射到视网膜上的视觉图像总是在不停地变化,而人类的感知系统依然可以准确高效地识别物体.因此,人类的感知系统有相应的快速处理机制以应对这种动态变化．然而,前人的实验都是在相对稳定的刺激条件下研究人类被试的感知系统对一个刺激参数的反应,比如在固定对比度下测试朝向分辨能力,或在固定朝向测定对比度分辨能力,而朝向和对比度同时变化时,人类对这两个参数的分辨能力仍然缺乏研究．因此,在本实验中,我们使用朝向和对比度同时变化的刺激,研究了人类被试对朝向和对比度的分辨能力．结果表明,在这种动态变化的条件下,被试对朝向和对比度的分辨阈值都有显著性的降低．而且,朝向分辨阈值降低的幅度与在固定对比度参数条件下的分辨阈值成负相关,即在固定对比度条件下朝向分辨阈值较高的被试,在朝向和对比度同时变化条件下,其朝向分辨阈值降低的幅度相对要大,朝向分辨能力也就相对地提高更大．对比度分辨能力也呈现同样的规律．这些结果说明,朝向和对比度的同时变化提高了被试对朝向和对比度的分辨能力,一个参数变化时其分辨能力越低的被试,两个参数变化时其分辨能力提高的幅度就越大．揭示了视觉系统处理这种多刺激参量信息变化的能力和机制,对人类视觉系统在真实的视觉过程中如何处理朝向和对比度信息提供了认识．     

基于频谱图像灰度共生矩阵的无损测温方法

本文提出了一种基于哈达玛变换的频谱图像灰度共生矩阵(Hadamard-GLCM)的高强度聚焦超声治疗无损测温方法。利用高强度聚焦超声辐照新鲜离体猪肉组织,获取辐照前后的B超图像的减影图像,采用Hadamard变换对其进行处理,获取频谱图像,将频谱图像的灰度共生矩阵惯性矩作为反应温度变化的信息参数。实验表明:不仅单组数据的Hadamard-GLCM惯性矩(HGMI)和温度能很好的线性拟合,而且多组数据的Hadamard-GLCM惯性矩与温度也成近似的线性关系,而且斜率非常接近,拟合度更接近1,误差小,对温度的分辨能力高,容错能力强,与传统的测温方法相比有着明显的优势,能为HIFU治疗过程中的无损测温提供有效的实时依据。     

自由飞行蜜蜂对静止目标形状和颜色的综合识别能力

研究了蜜蜂对相同颜色和不同颜色目标图对的形状以及颜色的综合识别能力实验过程中,蜜蜂始终处于自由飞行状态.做为刺激目标使用的图对分别有相同颜色不同几何形状、相同颜色不同拓扑结构和不同颜色几何形状三组.主要结果有三点:(1)在相同颜色的条件下,蜜蜂可以分辨出图形的几何形状,并且识别能力与图对的相似程度成反比(2)在刺激图形为环形时,蜜蜂对图形平均亮度敏感;在平均亮度相同的情况下,对环形细节变和尺寸大小不敏感.(3)在不同颜色不同几何形状的刺激条件下.蜜蜂视觉信息加工过程中颜色因素会抑制几何形状因素而起主要作用.这三个结果可以视为深入研究颜色加工通道和几何形状加工通道之间内在关系的基础.     

用于柑桔成熟度无损检测的色度频度序列法研究

农产品内部品质无损检测技术是确定水果最合适的采收期和对成熟度不一致的农产品进行准确分级的关键．为了建立利用计算机视觉技术进行柑桔成熟度的无损检测的方法,本研究建立了用于柑桔成熟度检测的计算机视觉系统,研究了柑桔图像颜色的描述方法,通过分析比较,认为在利用水果可见光彩色图像检测水果成熟度时,宜采用HSI颜色模型空间;提出了用与各个色度对应的像素在图像中出现的频度构成的频度序列描述图像的颜色信息的新方法,并利用人工神经网络方法建立了根据柑桔图像的色度频度序列判断柑桔成熟度的映射器,这一映射器检验252只成熟度不同的尾张系柑桔的结果为,对成熟果实和未熟果实的判断正确率分别为 79 1％和63．6％,总的判断正确率为77．8％,这表明尾张系柑桔果实的表皮颜色与成熟度之间具有相关性,可以通过利用计算机视觉技术测定柑桔的表皮颜色信息来判断柑桔的成熟度．     

初级视皮层神经元集群对拓扑特征响应的可视化表征

神经元集群响应的高维特性是脑机制研究面临的主要困难之一.拓扑特征是图像的基本特征之一,为了有效表征高维的神经元集群响应的拓扑特征特性,提出了一种基于三维自组织映射网络采用RGB颜色特征表征神经元集群响应的动态可视化方法,分析多通道微电极阵列采集的大鼠初级视觉皮层(V1区)神经元集群信号,进而研究了V1区神经元集群对图形拓扑特征的响应特性.通过与主成分分析(PCA)方法进行对比发现:该方法能够有效表征V1区神经元集群对拓扑结构的时序动态响应特征,表征方式形象直观,具有一定的优越性.     

心理意象加工的子系统的研究

目的:本文主要探索心理意象加工过程的子系统以及它们之间的相互关系。方法:实验设计了四种不同的二维心理意象任务:再现任务,分辨任务,旋转任务和空间任务,分别用来测量被试对整体图像信息的提取能力,细节意象能力,空间操作和空间认知等心理意象能力的不同方面。91名正常的大学本科生(77男,14女)参加了此次实验。结果:心理意象的整体再现和细节意象能力呈显著相关;空间旋转和空间认知能力呈显著相关;而其他能力之间无显著相关性。结论:实验结果表明心理意象加工过程主要分为相时独立的两个子系统,即对心理意象的再现和操作能力。     

Dichromatic and Trichromatic Callithrix geoffroyi Differ in Relative Foraging Ability for Red-Green Color-Camouflaged and Non-camouflaged food

An advantage for trichromatic color vision in primates is shown by its presence in many lineages, but little attention has been paid to the potential disadvantages of trichromacy. Most New World monkey species are polymorphic for color vision, with both dichromats and trichromats present within a single population. We tested the foraging ability of trichromatic and dichromatic Geoffroy's marmosets (Callithrix geoffroyi) for colored cereal balls (Kix®) under conditions of red-green color camouflage (orange/green Kix® against an orange/green background) or lack of camouflage (Kix® same color as background) in a naturalized captive setting. In separate experiments designed to test foraging ability at long distances (<6 m) and short distances (<0.5 m), trichromats found significantly fewer Kix® under the camouflage condition than in the non-camouflage condition. In contrast, there is no difference in the ability of dichromats to detect color-camouflaged versus non-camouflaged Kix®. There is no significant difference between dichromats and trichromats for either camouflaged or non-camouflaged Kix®, though the power in the tests is low because of high individual variation. The results have clear implications for the foraging strategies of trichromatic marmosets. Differences in intensity of competition between trichromats and dichromats for items of food of different colors in relation to background may also have consequences for the foraging behavior of dichromats.     

Demonstration of a genotype-phenotype correlation in the polymorphic color vision of a non-callitrichine New World monkey, capuchin (Cebus apella)

Color-vision polymorphism in New World monkeys occurs because of an allelic polymorphism of the single-copy red-green middle-to-long-wavelength-sensitive (M/LWS) opsin gene on the X chromosome. Because color-vision types can readily be estimated from allelic types of the M/LWS opsin gene, this polymorphic system offers researchers an excellent opportunity to study the association between vision and behavior. As a prerequisite for such studies, genetically determined color-vision types must be concordant with phenotypes determined directly by behavioral criteria (e.g., by a color discrimination test). However, such correlations between genotypes and phenotypes have been studied only for callitrichine species. Using genetic, electrophysiological, and behavioral approaches, we evaluated the color vision of brown capuchin monkeys (Cebus apella), a representative non-callitrichine model animal for physiology and behavior. Two allelic M/LWS opsins-P545 and P530-were identified in the studied captive population. Females had one or both of the alleles, and males had either one. The retinal sensitivity in P530 dichromats was short-wave shifted relative to that in P545 dichromats, whereas that in P530/P545 trichromats was between the two groups. In a discrimination task using Ishihara pseudo-isochromatic plates, P530/P545 trichromats were successful in discriminating stimuli that P530 and P545 dichromats were unable to discriminate. In a food-search task, P530/P545 trichromats were able to locate red targets among green distracters as quickly as among white distracters, whereas both types of dichromats took longer. These results demonstrate the mutual consistency between genotypes and phenotypes of color vision, and provide a solid genetic basis on which the ecology and evolution of color vision can be investigated.     

Color vision in marmosets and tamarins: behavioral evidence

Here we demonstrate differences in the relative performance of 15 callitrichids tested in a series of color visual discrimination experiments. Munsell color chips were chosen as stimuli based on their use in earlier experiments with human dichromats. We show behavioral evidence for the existence of four distinct kinds of color-vision phenotypes, each of which has slightly different color discrimination abilities. The different phenotypes may offer different advantages. The data are in accordance with the existence of a visual polymorphism in callitrichids.     

Using the Hard, Randy, and Rittler Test to Evaluate Color Vision in Capuchins (Cebus libidinosus)

The identification of color vision types in primates is fundamental to understanding the evolution and biological function of color perception. The Hard, Randy, and Rittler (HRR) pseudoisochromatic test categorizes human color vision types successfully. Here we provide an experimental setup to employ HRR in a nonhuman primate, the capuchin (Cebus libidinosus), a platyrrhine with polymorphic color vision. The HRR test consists of plates with a matrix composed of gray circles that vary in size and brightness. Differently colored circles form a geometric shape (X, O, or Δ) that is discriminated visually from the gray background pattern. The ability to identify these shapes determines the type of dyschromatopsy (deficiency in color vision). We tested six capuchins in their own cages under natural sunlight. The subjects chose between two HRR plates in each trial: one with the gray pattern only and the other with a colored shape, presented on the left or right side at random. We presented the test 40 times and calculated the 95?% confidence limits for chance performance based on the binomial test. We also genotyped all subjects for exons 3 and 5 of the X-linked opsin genes. The HRR test diagnosed two subjects as protan dichromats (missing or defective L-cone), three as deutan dichromats (missing or defective M-cone), and one female as trichromat. Genetic analysis supported the behavioral data for all subjects. These findings show that the HRR test can be applied to diagnose color vision in nonhuman primates.     

The Heterozygote Superiority Hypothesis for Polymorphic Color Vision Is Not Supported by Long-Term Fitness Data from Wild Neotropical Monkeys

The leading explanatory model for the widespread occurrence of color vision polymorphism in Neotropical primates is the heterozygote superiority hypothesis, which postulates that trichromatic individuals have a fitness advantage over other phenotypes because redgreen chromatic discrimination is useful for foraging, social signaling, or predator detection. Alternative explanatory models predict that dichromatic and trichromatic phenotypes are each suited to distinct tasks. To conclusively evaluate these models, one must determine whether proposed visual advantages translate into differential fitness of trichromatic and dichromatic individuals. We tested whether color vision phenotype is a significant predictor of female fitness in a population of wild capuchins, using longterm 26 years survival and fertility data. We found no advantage to trichromats over dichromats for three fitness measures fertility rates, offspring survival and maternal survival. This finding suggests that a selective mechanism other than heterozygote advantage is operating to maintain the color vision polymorphism. We propose that attention be directed to field testing the alternative mechanisms of balancing selection proposed to explain opsin polymorphism nichedivergence, frequencydependence and mutual benefit of association. This is the first indepth, longterm study examining the effects of color vision variation on survival and reproductive success in a naturallyoccurring population of primates.     

Fig Foraging by Dichromatic and Trichromatic <Emphasis Type="Italic">Cebus capucinus</Emphasis> in a Tropical Dry Forest

Figs are important resources for frugivores, and Ficus is an ideal taxon for evaluating patterns of primate foraging related to food color. Ficus spp. can be classified as conspicuous (color change from greenish to reddish during ripening) or cryptic (green throughout ripening). To investigate the effect on foraging of color vision phenotype variation for these 2 types of figs, we conducted a 20-mo study on 4 groups of white-faced capuchins (Cebus capucinus) in the Santa Rosa Sector of the ACG, Costa Rica between May 2004 and September 2008. We genotyped all individuals and collected behavioral data on feeding rates, acceptance indices, and foraging sequences. We found a significant effect of fig type; feeding rates and acceptance indices were higher for conspicuous figs than for cryptic figs, and subjects sniffed cryptic figs more often than conspicuous figs. We also found that dichromats sniffed more figs and had longer foraging sequences than trichromats, especially for cryptic figs. Among 6 subtypes of dichromats and trichromats, monkeys possessing the trichromat phenotype with the most spectrally separated L-M opsin alleles showed the highest acceptance index for conspicuous figs, though there were no differences in feeding rates among phenotypes. We conclude: 1) conspicuous figs are visually salient not only for trichromats but also for dichromats, 2) olfaction is important for evaluating edibility of cryptic figs, and 3) the reliance on olfaction for selecting fruit is greater in dichromats. These results indicate divergent foraging strategies among color vision phenotypes for assessing food items.     

Color Discrimination in the Tufted Capuchin Monkey,Sapajus spp

The present study evaluated the efficacy of an adapted version of the Mollon-Reffin test for the behavioral investigation of color vision in capuchin monkeys. Ten tufted capuchin monkeys (Sapajus spp., formerly referred to as Cebus apella) had their DNA analyzed and were characterized as the following: one trichromat female, seven deuteranope dichromats (six males and one female), and two protanope males, one of which was identified as an “ML protanope.” For their behavioral characterization, all of the subjects were tested at three regions of the Commission International de l''Eclairage (CIE) 1976 u′v′ diagram, with each test consisting of 20 chromatic variation vectors that were radially distributed around the chromaticity point set as the test background. The phenotypes inferred from the behavioral data were in complete agreement with those predicted from the genetic analysis, with the threshold distribution clearly differentiating between trichromats and dichromats and the estimated confusion lines characteristically converging for deuteranopes and the “classic” protanope. The discrimination pattern of the ML protanope was intermediate between protan and deutan, with confusion lines horizontally oriented and parallel to each other. The observed phenotypic differentiation confirmed the efficacy of the Mollon-Reffin test paradigm as a useful tool for evaluating color discrimination in nonhuman primates. Especially noteworthy was the demonstration of behavioral segregation between the “classic” and “ML” protanopes, suggesting identifiable behavioral consequences of even slight variations in the spectral sensitivity of M/L photopigments in dichromats.     

Dichromatic color language: "reds" and "greens" don't look alike but their colors do.

When protanopes or deuteranopes arrange the Farnsworth Dichotomous Test colors in order of similarity, they reveal their lack of red/green hue discriminations by alternating chips that the normal trichromat sees as reddish and greenish test colors. The dichromatic orderings follow a systematic variation in saturation of blue hues through neutral and into yellow hues as described by theory for each of the two types. Some dichromats who show the typical test behavior nevertheless use reddish and greenish hue terms appropriately when instructed to name the same test colors. Lightness cues are probably used by these dichromats in the naming task but ignored in the perceptual similarity task. Thus, unlike normal trichromats, who use similar names for perceptually similar colors, dichromats may use dissimilar names for perceptually similar colors. In this way they can achieve concordance with the normative language system despite its discordance with their impoverished color perceptions.     

THE COLOR VISION OF DICHROMATS : I. WAVELENGTH DISCRIMINATION,BRIGHTNESS DISTRIBUTION,AND COLOR MIXTURE

1. Protanopes and deuteranopes show one maximum of wavelength discrimination which occurs near their neutral point in the region of 500 mµ (blue-green for color-normal). The value of the just discriminable wavelength interval Δλ is about 1 mµ at this point and is much like the normal. To either side of this, Δλ rises. It increases rapidly on the short-wave side, and slowly on the long-wave side, rising to about 50 mµ at the two ends of the spectrum. 2. The brightness distribution in the spectrum for dichromats falls only partly outside the range established for color-normals. The protanope curve is narrower than normal, and its maximum lies nearly 15 mµ to the left of it. The deuteranope curves are about the same width as the normal, and their maxima lie slightly but definitely to the right of it. The main difference between protanope and deuteranope spectrum sensitivity lies on the red side of brightness curves, where the deuteranope is strikingly higher. This difference furnishes the only reliable diagnostic sign which may be applied to an individual dichromat for separating the two types. 3. The average position for the neutral point of twenty-one protanopes is 496.5 mµ; of twenty-five deuteranopes 504.3 mµ. The range of variation in the position of neutral point is twice as great for the deuteranope as for the protanope. 4. Dichromatic gauging of the spectrum cannot yield unique mixture values for any wavelength because of the large stretches of poor wavelength discrimination. Data have therefore been secured which locate the spectral ranges that can match specific mixtures of two primaries when brightness differences are eliminated. The form of the data is much the same for a protanope and for a deuteranope; the only difference is in the relative brightness of the primaries. 5. Previously accepted anomalies in the spectral matching of dichromats which have led to the rejection of the third law of color mixture for them, have been eliminated. They are shown to have been due to the non-uniqueness of color matches and the usually disparate brightnesses of the primaries. Color mixture matches for dichromats are valid at all brightnesses.     

Bone surface mapping method

Bone shape is an important factor to determine the bone's structural function. For the asymmetrically shaped and anisotropically distributed bone in vivo, a surface mapping method is proposed on the bases of its geometric transformation invariance and its uniqueness of the principal axes of inertia. Using spiral CT scanning, we can make precise measurements to bone in vivo. The coordinate transformations lead to the principal axes of inertia, with which the prime meridian and the contour can be set. Methods such as tomographic reconstruction and boundary development are employed so that the surface of bone in vivo can be mapped. Experimental results show that the surface mapping method can reflect the shape features and help study the surface changes of bone in vivo. This method can be applied to research into the surface characteristics and changes of organ, tissue or cell whenever its digitalized surface is obtained.