Brightness as a function of retinal locus

Brightness functions were determined for the dark-adapted fovea and periphery. In one series of experiments, observers matched numbers to the brightness of a 1° white target at various intensities, presented half the time to the fovea, the other half to one of five peripheral loci: 5°, 12°, 20°, 35°, and 60°. In a second series, observers matched the brightness of a 1° white target in the fovea of one eye to the brightness of an identical target in the periphery of the other eye at various intensities. Thresholds were also determined for the fovea and for the five peripheral loci by a staircase procedure. The magnitude estimations and the interocular matches concur in showing that a stimulus of fixed luminance appears brighter in the periphery than in the fovea. The brightness was found to be maximal at 20°. Brightness grows as a similar power function of luminance at all six retinal positions.     

Brightness as a function of retinal locus

Brightness functions were determined for the dark-adapted fovea and periphery. In one series of experiments, observers matched numbers to the brightness of a 1° white target at various intensities, presented half the time to the fovea, the other half to one of five peripheral loci: 5°, 12°, 20°, 35°, and 60°. In a second series, observers matched the brightness of a 1° white target in the fovea of one eye to the brightness of an identical target in the periphery of the other eye at various intensities. Thresholds were also determined for the fovea and for the five peripheral loci by a staircase procedure. The magnitude estimations and the interocular matches concur in showing that a stimulus of fixed luminance appears brighter in the periphery than in the fovea. The brightness was found to be maximal at 20°. Brightness grows as a similar power function of luminance at all six retinal positions.     

Perceived roughness as a function of body locus

Twenty subjects made magnitude estimates of the roughness of grooved metallic surfaces applied to 10 body loci. To a first approximation, perceived roughness grew as a power function of groove width, in accordance with earlier studies. The exponents and intercepts (up-down position in log-log coordinates) of the power function turn out to depend strongly on body locus. The straight lines in log-log coordinates tend to diverge with groove width so that differences among body loci are especially pronounced at large groove widths. Sensitivity to roughness was greatest for the lips, fingers, and forearm, and least for the heel, back, and thigh. The rank order of the body loci in terms of roughness sensitivity closely parallels the rank order for punctate pressure sensitivity, as reported by von Frey in 1894, but apparently not for other measures of tactile sensitivity, such as vibration thresholds to various frequencies, two-point thresholds, and error of point localization.     

Border contrast as a function of retinal locus

When the visibility of a small test spot was measured by direct brightness matching at various locations along the white edge of a black and white border, it was found that the white background was perceived as becoming progessively brighter as the border was approached. The effect was greater when a corner was neared. Moreover, greater effects, i.e., larger differences between the edge effect and base level (no border) were found at distances farther removed from the fovea (0 deg 12 min to 3 deg 52 min).     

Retroactive inhibition as a function of the locus of categorized response sets

The effects which list-level taxonomic attributes should have upon retroactive inhibition (RI) producing mechanisms in both response-set interference theory (Postman & Stark, 1969) and Petrich’s (1975) retrieval model are discussed. A test of the theories was performed by manipulating the presence (1) or absence (0) of categorized response sets in both original learning (OL) and interpolated learning IIL), and comparing their predictions concerning the relative degree of RI expected in the four conditions (0-0, 0-1, 1-0, 1-1). In line with Petrich’s predictions, OL categorization significantly reduced RI, IL categorization significantly increased RI, and 0-1 produced significantly greater RI than 1-0. Moreover, the obtained ranking of the means for the experimental groups in degree of RI (0–1>0-0>1-0 ? 1-1) was in close agreement with the ranking predicted by Petrich’s (1975) model. The results provide support for Petrich’s (1975) retrieval model and pose explanatory problems for response-set interference theory (Postman & Stark, 1969).     

预期错误在恐惧记忆更新中的作用与机制

依据错误驱动的学习理论,行为预期结果与实际结果之间的不匹配即预期错误(Predictionerror,PE)是学习产生的驱动因素。作为显著性信息中的一种,预期错误和物理显著性、惊讶、新异性等存在信息加工阶段的不同,与记忆更新的关系也有差异。近年来,记忆再巩固干预范式(reconsolidation interference)被证明可用于人类条件性恐惧记忆的更新,其中记忆提取激活阶段所包含的预期错误起到了引发记忆“去稳定”、开启记忆再巩固的关键作用。在促进恐惧记忆更新的行为机制上,PE被认为是记忆去稳定的必要非充分条件。记忆提取必须包含适量的PE,但其引发的是记忆去稳定、消退还是中间状态,还需结合记忆本身性质确定。在促进恐惧记忆更新的神经机制上,杏仁核、导水管周围灰质(PAG)、海马均在PE探测和计算过程中具有重要作用;前额叶皮层(PFC)及其亚区在PE开启记忆再巩固过程中扮演了重要角色。上述过程又受到神经系统中特定神经递质的重要调节,尤其是多巴胺能和谷氨酸能。未来研究应进一步探索基于PE计算模型的量化研究,整合PE与其他边界条件的交互作用,考察不同类型显著性在记忆再巩固中的作用等;并亟...     

Duration of the motion aftereffect as a function of retinal locus and visual field.

The duration of the aftereffect induced by viewing a rotating disc was recorded separately for the four hemiretinae of the left and right eyes using a new method of measurement. The results showed duration of aftereffect to differ between nasal and temporal hemiretinae of the right eye and between left and right cerebral hemispheres.     

Visual detection as a function of attentional demand and perceptual system error

Attentional demands were varied in a two-alternative, forced-choice detection experiment. A bar indicator designated the target form in one condition and occurred in random locations in a second condition. Exposure durations necessary for predetermined single-form display HRs were determined for each of eight Ss to measure performance at different levels of perceptual system error. Forms differed in only a single feature. Detection was superior when the bar indicator designated the target form, and differences increased with increased display size. Evidence for interference in detection due to the presence of nontarget forms apart from noting requirements of such forms was found. Estimates of number of perceptual channels noted did not clearly differentiate serial from parallel processing models. It was concluded that display interference error and spatial selectivity influences are important determinants of detection accuracy.     

The error in the error theory

Moral error theory of the kind defended by J. L. Mackie and Richard Joyce is premised on two claims: (1) that moral judgements essentially presuppose that moral value has absolute authority, and (2) that this presupposition is false, because nothing has absolute authority. This paper accepts (2) but rejects (1). It is argued first that (1) is not the best explanation of the evidence from moral practice, and second that even if it were, the error theory would still be mistaken, because the assumption does not contaminate the meaning or truth-conditions of moral claims. These are determined by the essential application conditions for moral concepts, which are relational rather than absolute. An analogy is drawn between moral judgements and motion judgements.     

Human taste response as a function of locus of stimulation on the tongue and soft palate

Taste recognition thresholds and psychophysical intensity functions were determined for NaCl, sucrose, QHC1, urea, and citric acid for four loci on the tongue and on the soft palate. The results showed greater differences between loci than previously reported. Contrary to older data, the threshold for bitter was found to be lower for the fungiform papillae at the front of the tongue and for the soft palate than for the vallate papillae. For all compounds, the slopes of the intensity functions varied with the locus of stimulation. The functions for most compounds were steepest at the vallate and foliate loci.