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A nonlinear systems approach to Fechner's paradox.

It is possible to predict the topology of isointensity plots under conditions of extreme imbalance of the stimulus inputs, without making any assumptions specific to the circumstances in which Fechner's Paradox is sometimes observed. This is done by extending a nonlinear model for a sensory channel, by postulating a form of cross-coupling or interference between two channels which represents other phenomena in psychophysics. It is noted that the form in which data are usually reported is not an adequate basis for testing all the predictions of a nonlinear model in sensory psychophysics. The physiologist Panum (1958), and later Fechner (1860) reported that the apparent brightness of an object viewed binocularly could, under conditions where the input to one eye was diminished by filtering, be less than its brightness viewed monocularly by the unfiltered eye. To a first approximation, binocular brightness is more like an averaging of two monocular inputs than a summation of those same inputs. For over 120 years this phenomenon, which came to be called "Fechner's Paradox", though Panum should perhaps have had some credit, has been the subject of experimental investigation and associated mathematical modelling. If one consults a dictionary of psychological terms, for example Evans (1978), one may read something like Fechner's Paradox: The name give to the observation that something [which is] viewed binocularly seems to increase in brightness when one eye is closed. And yet we now know that this definition is misleading, because the same phenomenon in pooling two sensory inputs has its analogues in audition (Lehky 1983) and in olfaction (Gregson 1986). Gilchrist and McIver (1985) have now shown an analogue of the paradox exists in ocular contrast sensitivity. The definition also goes awry when the input luminance to one eye is zero, or when the luminance and ocular adaptation are closely matched for the two eyes. It is wiser, in the light of results reporting individual differences in the existence and extent of the paradox, and its sensitivity to stimulus conditions, to side with Blake and Fox (1973) when they observed that it is not unreasonable to suppose that various stimulus conditions might yield varying amounts of summation or even inhibition. Empirical reviews of relevant data in vision have been given by Roelofs and Zeeman (1914), Blake and Fox (1973), and Blake et al. (1981), but a theoretical model of interest as a starting point is that of Lehky (1983).

Computer Simulation↗

Acquired Nystagmus.

Patients with acquired forms of nystagmus may suffer from oscillopsia and blurred vision; abolishing or reducing nystagmus ameliorates these symptoms. Ideally, treatment of nystagmus should be directed against the pathophysiologic mechanism responsible. Identification of nystagmus pattern is important in directing therapy and occasionally requires electronic eye movement recording for precise characterization. Patients with acquired pendular nystagmus, particularly those with multiple sclerosis, often benefit from gabapentin, a drug with few side effects. Scopolamine, clonazepam, and valproate are also useful in some patients. A new drug, memantine, was effective in treating pendular nystagmus in one study, but it has not yet been approved for use in the United States. Periodic alternating nystagmus usually responds to baclofen. Central vestibular nystagmus, including downbeating and upbeating forms, can be treated with baclofen or clonazepam. In some patients, treatment of an underlying condition, such as periodic ataxia, Whipple's disease, and Chiari malformation, abolishes nystagmus and improves vision. If pharmacologic therapy fails, optical devices can be considered in selected patients. Injections of botulinum toxin and surgery to weaken extraocular muscles are prone to induce diplopia and may precipitate plastic-adaptive ocular motor changes that eventually negate the beneficial effect.

Journal Article↗

The cerebellar control of accommodation of the eye in the cat.

The effect of cerebellar stimulation on the accommodation of the lens was examined in anesthetized cats. An infrared optometer was used to measure the refractive power of the lens during stimulation of the cerebellum. The area giving responses within latencies shorter than 160 msec and amplitudes larger than 0.15 diopters is localized in the contralateral interpositus and fastigial nuclei and the ipsilateral interpositus nucleus. No responses could be evoked by stimulating the bilateral lateral nuclei. Accommodation responses were also evoked by cerebellar cortex stimulation. Accommodation responses evoked by stimulating the cerebellar nuclei were inhibited by preceding cerebellar cortical stimulation.

Accommodation, Ocular↗

Developmental trends in the understanding of perceptual adaptation.

In the first of three studies, kindergartners, third graders, and sixth graders were questioned to determine whether they comprehend five types of perceptual adaptation or contrast effects. The results indicated little consistency among kindergartners, but there were strong improvements by the third-grade level, and at the sixth-grade level almost all of the children were showing perfect performance, demonstrating comprehension of the five forms of perceptual adaptation. In the second and third studies, children and adults were placed in a situation in which adaptation to temperature and weight could occur, and they were asked to predict subsequent perceptions. Correct performance in these studies generally occurred at later ages than in Study 1 with even college students showing incorrect performance in some cases. However, the age trends shifted quite markedly depending upon the nature and structure of the task. The results were consistent with a theory stressing the relation of early formed schemas in the form of memory traces of experiences to later appearing and more abstract schemas. The results show the importance of studying older children when considering developing theories of mind.

Adaptation, Ocular↗

Natural problems for stereoscopic depth perception in virtual environments.

The use of virtual reality (VR) display systems has escalated over the last 5 yr and may have consequences for those working within vision research. This paper provides a brief review of the literature pertaining to the representation of depth in stereoscopic VR displays. Specific attention is paid to the response of the accommodation system with its cross-links to vergence eye movements, and to the spatial errors that arise when portraying three-dimensional space on a two-dimensional window. It is suggested that these factors prevent large depth intervals of three-dimensional visual space being rendered with integrity through dual two-dimensional arrays.

Accommodation, Ocular↗

Seeing the light: Adapting luminance reveals low-level visual processes in the attentional blink.

It is widely assumed that high-level visual processes subserve the attentional blink (AB). Recent evidence from studies of visual masking during the AB that were designed to directly test the contributions of high-level masking effects, however, have failed to provide empirical support for this position. The implication is that low-level visual processes are crucial to the AB. We tested this idea by manipulating adapting luminance in a standard AB paradigm. Consistent with the involvement of low-level neural mechanisms, the AB effect interacted with adapting luminance such that an AB was revealed only under photopic (light adapted) viewing conditions.

Adaptation, Ocular↗

Visual complaints from healthy children.

It is common for healthy children with specific visual complaints to be seen for eye examinations. After a complete eye examination has ruled out pathologic conditions as the cause of these complaints, it is appropriate for the clinician to explore the possibility that normal entoptic or physiologic visual phenomena might have provoked the child's report of vision problems. Some of these normal visual experiences are frequent causes of children's complaints of vision problems, such as physiologic diplopia, relaxation of the near synkinesis during reading, and vitreous body floaters. Some complaints are common, even though the underlying entoptic or physiologic phenomenon may be speculative or obscure, such as the report that objects look bigger or smaller than they actually are. When the clinician encounters such situations, the parents and the child will be much more satisfied by an explanation of the normal system anatomy and physiology than by the simple reassurance that everything is all right.

Accommodation, Ocular↗

Orientation- and frequency-modulated textures at low depths of modulation are processed by off-orientation and off-frequency texture mechanisms.

Intuitively it may seem likely that orientation-modulated (OM) and frequency-modulated (FM) textures are processed utilizing the first-order channels that are most responsive to the first-order (luminance) information contained in the textures. This assumption would imply that the detection or segmentation of OM or FM textures is accomplished by second-order mechanisms that receive their first-order input from neurons tuned to either the center, or to the peaks in the orientation and spatial-frequency distribution of the texture. Here we show that at low depths of modulation this is not the case. Using an adaptation paradigm, we show that the first-order filters involved in the perception of OM and FM textures are those which maximize the differential response between the different texture regions. Our explanation of this result is similar to that made by Regan and Beverley [J. Opt. Soc. Am. 73 (1983) 1684; J. Opt. Soc. Am. A 2 (1985) 147] for simple grating stimuli. However, we show that whereas Regan and Beverley's results could be accounted for on the basis of the tuning functions of the putative mechanisms involved, our results can be explained in terms of the characteristics of the textures themselves. Some implications of our finding are discussed.

Adaptation, Ocular↗