不同运动速度下人眼的阈上调制特性

本文报道了在光栅的三种恒定运动速度(0°/S,10°/S,30°/S)下,阈值对比敏感度函数CSF(V)和阈上对比度比配函数CMF(V,C)的测试数据.计算机拟合结果表明,在各个不同的恒定运动速度下,人眼的阈上对比度比配函数CMF(V,C)和阈值对比敏感度函数CSF(V),可以由静止目标的阈值对比敏感函数CSF近似地预测出来.本文给出了预测方法的数学描述及有关经验公式.     

视觉系统初级信息加工的一种数学模型——<Ⅰ>模型的空间性质

本文用广义Gabor(EQ)函数作为视觉系统进行初级信息加工的核函数.所谓广义Gabor函数,就是把原始Gabor函数中的一个独立变量扩展到三个(即空间变量从一维推广到二维,再加时间变量),并相应地引入一些参数.本文中EG取二大类形式:各向同性系统中表达式和各向异性系统表达式.当EG取某一特定形式,而且其中参数取某些特定值时,本模型可分别定性描述电生理实验中发现的几种主要感受野类型(Kuffler,Hubel和Wiesel型等).在空间频率域中引入对数变换假设后,EG经付里叶变换后可很好地合成人眼调制传递函数(MTF)     

用生理数据和光学方法模拟视觉系统的空间滤波特性

实验采用光学滤波的方法,根据人类视觉系统对比敏感度曲线的生理数据,制作了一种模拟视觉系统空间调制传递特性的“人眼滤波器”.并用该滤波器对视错觉三角进行了分析.     

用显示器测量办公亮度环境下的人眼对比度敏感视觉特性

对比度敏感是描述人眼视觉系统空间特性的主要指标之一,对比度敏感函数是反映不同条件下的对比度敏感与空间频率之间的关系。人眼对比度敏感数据的测量受到环境亮度较大的影响,为了研究常用办公环境条件下的人眼对比度敏感情况,对6位青年在环境亮度分别为153,312,470 cd/m2和暗室条件下,在距离为2米处观测11种空间频率的矩形光栅进行测量,光栅用显示器进行显示,其平均亮度分别为60和90 cd/m2。实验结果表明,对于相同频率的光栅,人眼对比度敏感程度随着环境亮度的增加而减小,而且人眼在暗室环境下比在办公环境条件下对亮度光栅更敏感;但是在观测平均亮度为60cd/m2的光栅时,人眼特殊地对在环境亮度为312 cd/m2的条件下更敏感。     

用显示器测量办公亮度环境下的人眼对比度敏感视觉特性

对比度敏感是描述人眼视觉系统空间特性的主要指标之一,对比度敏感函数是反映不同条件下的对比度敏感与空间频率之间的关系。人眼对比度敏感数据的测量受到环境亮度较大的影响,为了研究常用办公环境条件下的人眼对比度敏感情况,对6位青年在环境亮度分别为153,312,470 cd/m2和暗室条件下,在距离为2米处观测11种空间频率的矩形光栅进行测量,光栅用显示器进行显示,其平均亮度分别为60和90 cd/m2。实验结果表明,对于相同频率的光栅,人眼对比度敏感程度随着环境亮度的增加而减小,而且人眼在暗室环境下比在办公环境条件下对亮度光栅更敏感;但是在观测平均亮度为60cd/m2的光栅时,人眼特殊地对在环境亮度为312 cd/m2的条件下更敏感。     

对比度检测学习提高猫的视觉对比敏感度

对人的心理学研究结果显示,对比度检测学习可提高学习者对视觉刺激的对比敏感度,但其潜在的神经机制尚不清楚。该研究用二选一（two-alternative forced choice）方法训练3只猫（Felis catus）通过单眼进行对比度检测学习,发现每只猫对视觉刺激的对比敏感度随着训练而显著提高。该学习效果虽然对训练眼有明显的特异性,但部分学习效果可以传递给非训练眼,提示对比度检测学习可能会引起双眼信息汇聚前后的视觉中枢的神经可塑性。另外,猫视觉对比敏感度的提高主要发生在训练刺激的空间频率附近,表明对比度检测学习具有一定的空间频率选择性。该研究结果显示,猫对视觉刺激的对比度检测学习表现出与人类相似的特性,因此可以作为模式动物来研究人类学习诱导的视觉对比敏感度升高的神经机制。     

大鼠听觉反应阈的测定

应用微电极技术测定了45只大鼠325根单一听神经纤维的特征频率及其阈值和调谐曲线。测得特征频率的最低值为0.58kHz,最高值为62.6kHz。敏感度最高的频带在20～50kHz,敏感度最高的阈值为6dB(SPL),其相应的频率为27.49kHz。由最低阈值连线延续到边侧的调谐曲线,便形成了大鼠整个的听反应阈曲线。该听反应阈曲线与行为测听所观察到的听力曲线近似。     

最大熵模型在物种分布预测中的优化

最大熵模型在物种分布的预测研究中得到广泛应用,但未经优化的模型的预测结果可能存在严重的拟合偏差.本文汇总了最大熵模型在取样偏差修正、模型复杂性调整、物种分布判定阈值选择以及模型检验过程中的若干优化方法.在取样偏差的修正中,空间筛除法的修正效果最好,而背景限制法表现不佳.模型复杂性受建模变量的数量、函数模式和调控系数的影响.在样本量小于建模变量的数量时需进行变量筛选,筛选标准应侧重其生态学意义,而非变量间的相关性;函数模式对模型表现影响不大,在预测结果相近情况下应选择简单模型;建模时需要调整调控系数以控制过度拟合,一般最优模型调控系数高于默认值.判定物种出现阈值应遵从客观性、等效性和判别力3个原则,敏感度和特异性加和最大是良好的阈值判定标准.模型检验可分为不依赖阈值的检验和依赖阈值的检验,在不依赖阈值的模型评估方法中,基于信息标准选择的模型表现优于基于AUC或相关系数(COR)选择的模型;在基于阈值的模型评估方法中,真实技能统计能够兼顾模型遗漏误差和错判误差,不受假设缺失影响,且受物种流行度的影响较小.     

光栅显示装置的试制和人眼对比敏感度的测定

本文报道了一个在普通示波器荧光屏上产生光栅和测量对比的方法。由于屏上的光点有一定大小和特殊的光晕,对比度和输入电压线性关系的丧失较快;我们只能测准每厘米(屏上)产生12对线的光栅。用主诉方法,测量了两名受试者的对比敏感度函数,并指出了用这方法测定该函数所带来的微小的不准确性.     

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．     

Lateral sensitivity modulation explains the flanker effect in contrast discrimination

We used a dual-masking paradigm to study how contrast discrimination can be influenced by the presence of adjacent stimuli. The task of the observer was to detect a target superimposed on a pedestal in the presence of flankers. The flankers (i) reduce the target threshold at zero pedestal contrast, (ii) shift the target threshold versus pedestal contrast (TvC) function horizontally to the left on a log-log plot at high pedestal contrasts, and (iii) reduce the size of pedestal facilitation at low pedestal contrasts. The horizontal shift at high pedestal contrasts suggests that the flanker effect is a multiplicative factor that cannot be explained by previous models of contrast discrimination. We extend the divisive inhibition model of contrast discrimination by implementing the flanker effect as a lateral multiplicative sensitivity modulation. This extended model provides a good account of the data.     

Measurement of visual channels by contrast adaptation.

Inspection of a high-contrast grating pattern affects our ability to detect patterns that are similar. This technique can be used to infer the underlying mechanisms of the visual system. By using this technique, measurements of the bandwidth of orientation channels are taken for different levels of adapting contrast and adapting duration. If the threshold elevation is plotted as the difference between the unadapted and adapted threshold in decibels, then the orientation bandwidth is invariant if taken at some fraction of the maximum elevation. This results from the fact that, as the orientation difference between the adapting and test patterns increases, the function relating threshold elevation to adapting contrast reduces in slope. These data contradict the often-used 'equivalent contrast transformation' (in which the fall off in the adaptation effect with respect to orientation is expressed in terms of an equivalent reduction in adapting contrast) as this would produce quite different bandwidths at different adapting contrasts. The data also address the issue of the neuronal mechanisms of adaptation.     

Changes in perceived contrast of suprathreshold gratings as a function of orientation and spatial frequency

Orientation anisotropy for suprathreshold gratings of different spatial frequencies was measured using a contrast matching procedure. Observers matched the contrast of sine-wave gratings of various orientations to a vertical reference grating set at different reference contrasts. At threshold, the size of the anisotropy increased with spatial frequency, confirming previous results. When the reference grating contrast was set above threshold, the anisotropy declined, and eventually disappeared for gratings of medium spatial frequencies. At higher spatial frequencies, although the relative anisotropy became smaller, it did not disappear within the range of contrasts used in this study. For medium, but not for high spatial frequencies, the data are consistent with Kulikowski's (1976) model of effective contrast constancy.     

Measurement and modeling of peripheral detection and discrimination thresholds

This report describes experimental measurements of threshold contrasts as a function of the angle to the visual axis (peripheral threshold contrasts). The visual tasks consist in detection (perception of presence) and discrimination (perception of a form feature) of simple visual signs during a fixation period realistic observing conditions being chosen. Proceeding from the experimental findings a model for forecasting off-axis threshold contrast functions on different visual conditions is developed based upon spatial frequency filters. Further with the aid of a known model visibility fields are calculated.     

The spatial frequency discrimination function at low contrasts

Spatial frequency difference thresholds for sinewave gratings near contrast threshold were measured using a two-alternative forced-choice technique, and the threshold frequency differences were plotted as a proportion of standard frequency for standards from 2 to 7 cycles/degree. This function shows reliable local maxima and minima, and these features are more pronounced than they are when stimuli of 30% contrast are used. This result is consistent with the notion that at low contrasts, fewer spatial frequency channels are above threshold in the area of the visual field covered by the stimulus than when the stimulus is at high contrast.     

Sex & vision I: Spatio-temporal resolution

ABSTRACT: BACKGROUND: Cerebral cortex has a very large number of testosterone receptors, which could be a basis for sex differences in sensory functions. For example, audition has clear sex differences, which are related to serum testosterone levels. Of all major sensory systems only vision has not been examined for sex differences, which is surprising because occipital lobe (primary visual projection area) may have the highest density of testosterone receptors in the cortex. We have examined a basic visual function: spatial and temporal pattern resolution and acuity. METHODS: We tested large groups of young adults with normal vision. They were screened with a battery of standard tests that examined acuity, color vision, and stereopsis. We sampled the visual system's contrast-sensitivity function (CSF) across the entire spatio-temporal space: 6 spatial frequencies at each of 5 temporal rates. Stimuli were gratings with sinusoidal luminance profiles generated on a special-purpose computer screen; their contrast was also sinusoidally modulated in time. We measured threshold contrasts using a criterion-free (forced-choice), adaptive psychophysical method (QUEST algorithm). Also, each individual's acuity limit was estimated by fitting his or her data with a model and extrapolating to find the spatial frequency corresponding to 100 % contrast. RESULTS: At a very low temporal rate, the spatial CSF was the canonical inverted-U; but for higher temporal rates, the maxima of the spatial CSFs shifted: Observers lost sensitivity at high spatial frequencies and gained sensitivity at low frequencies; also, all the maxima of the CSFs shifted by about the same amount in spatial frequency. Main effect: there was a significant (ANOVA) sex difference. Across the entire spatio-temporal domain, males were more sensitive, especially at higher spatial frequencies; similarly males had significantly better acuity at all temporal rates. CONCLUSION: As with other sensory systems, there are marked sex differences in vision. The CSFs we measure are largely determined by inputs from specific sets of thalamic neurons to individual neurons in primary visual cortex. This convergence from thalamus to cortex is guided by cortex during embryogenesis. We suggest that testosterone plays a major role, leading to different connectivities in males and in females. But, for whatever reasons, we find that males have significantly greater sensitivity for fine detail and for rapidly moving stimuli. One interpretation is that this is consistent with sex roles in hunter-gatherer societies.     

The relation between visual acuity and brightness discrimination

1. Visual acuity depends on the brightness contrast between test object and background; and conversely, brightness discrimination depends on the target size. Both functions vary with the brightness of the background. Measurements with rectangular targets of length-width ratio 2 were made over a range of sizes, contrasts, and brightnesses sufficient to determine the relations among these three variables. The rectangles were from 2' to 50' wide; the contrast fraction, DeltaI/I, ranged from 0.01 to 40; the background brightness varied from 0.0001 to 2500 millilamberts. 2. When DeltaI/I or visual acuity is plotted as a function of brightness the data do, in general, follow Hecht's equation. The departure from a simple photochemical theory which the larger targets show is probably due to changes in the functional retinal mosaic with changing brightness. 3. In general also, the relation between visual acuity and brightness, at selected contrasts, fits Hecht's derivation. At low contrasts, as the brightness is reduced a point is reached at which the test object becomes invisible at any size. 4. No simple relation emerges from the data relating visual acuity to contrast, at set levels of illumination. Over only a very short range are visual acuity and contrast directly related. At high contrasts, visual acuity reaches a maximum, whereas at low visual acuity, DeltaI/I reaches a minimum which cannot be passed regardless of size. 5. The shape of the curves relating DeltaI/I to brightness is not significantly altered by changing the exposure time. There is some evidence to show that a 3 second exposure of the target is equivalent to two looks of 0.2 second each. 6. In all these studies the thresholds were determined by a frequency of seeing method, and the data have been considered in terms of a quantum theory of threshold seeing. It was found that a threshold response involves between four and eight independent critical events, which are largely independent of size, brightness, and criterion of seeing.