The nature and duration of adaptation following long-term odor exposure

Any individual living or working in an odorous environment can experience changes in odor perception, some of which are long lasting. Often, these individuals report a significant reduction in the perception of an odor following long-term exposure to that odor (adaptation). Yet, most experimental analyses of olfactory adaptation use brief odorant exposures which may not typify real-world experiences. Using a procedure combining long-term odor exposure in a naturalistic setting with psychophysical tests in the laboratory, we present evidence to show that reduced odor intensity following long-term exposure is accompanied by odorant-specific shifts in threshold. Subjects were exposed continuously to one of two odorants while in their home for a period of 2 weeks. Exposure produced an odorant-specific reduction in sensitivity and perceived intensity compared with preexposure baselines: Detection thresholds for the adapting odorant were elevated following exposure and perceived intensity ratings for weak concentrations were reduced. For most individuals, reduced sensitivity to the test odorant was still evident up to 2 weeks following the last exposure. The persistence of the change, as evidenced by the duration of recovery from adaptation, distinguishes this phenomenon from the adaptation seen following shorter exposures and highlights the need for the study of exposure durations that are more similar to real-world exposures.     

Brain stimulation and conscious experience

Libet discovered that a substantial duration (> 0.5-1.0 s) of direct electrical stimulation of the surface of the somatosensory cortex at threshold currents is required before human subjects can report that a conscious somatosensory experience had occurred. Using a reaction time method we confirm that a similarly long stimulation duration at threshold currents is required for activation of elementary visual experiences (phosphenes) in human subjects following stimulation of the surface of the striate cortex. However, the reaction times for the subject to respond to the cessation of the visual experience after the end of electrical stimulation could be as brief as 225-242 ms. We also carried out extensive studies in cats under a variety of anesthetic conditions using the same electrodes and parameters of stimulation employed in the human studies to study the patterns of neuronal activity beneath the stimulating surface electrode. Whereas sufficiently strong currents can activate neurons within milliseconds, stimulating currents close to threshold activate sustained neural activity only after at least 350-500 ms. When currents are close to threshold, some neurons are inhibited for several hundreds of millisecond before the balance between inhibition and excitation shifts towards excitation. These results suggest that the prolonged latencies, i.e., latencies beyond 200-250 ms, for the emergence of conscious experience following direct cortical stimulation result from a delay in the sustained activation of underlying cortical neurons at threshold currents rather than being due to any unusually long duration in central processing time. Intracellular records from cortical neurological cells during repetitive electrical stimulation of the surface of the feline striate cortex demonstrate that such stimulation induces a profound depolarizing shift in membrane potential that may persist after each stimulus train. Such a depolarization is evidence that extracellular K+ concentrations have increased during electrical stimulation. Such an increase in extracellular K+ progressively increases cortical excitability until the threshold for sustained activation of cortical neurons is reached and then exceeded. Consequently, the long latency for threshold activation of cortical neurons depends upon a dynamically increasing cortical facilatory process that begins hundreds of milliseconds before there is sustained activation of such neurons. In some cases, this facilatory process must overcome an initial stimulus-induced inhibition before neuronal firing commences.     

Stereoscopic perception with brief exposures

In this report we describe the results of an experiment in which we demonstrated that a powerful and compelling stereoscopic experience is elicited with very brief (< 1 msec) stimulus durations. The observers were highly successful in recognizing briefly flashed, stereoscopic, random-dot surfaces in the absence of monocular contours. The results are shown to be closely related to the range of depths for any stimulus form; however, the recognition thresholds were nonmonotonic as a function of disparity. Previous investigators have disagreed about the existence of a temporal threshold for stereopsis. We believe that prior findings suggesting that stereopsis cannot occur at short exposure durations are probably due to inadequate control of fixation disparity. Therefore, there is poor dichoptic image registration when a stereoscopic stimulus is presented. The present results also raise difficulties for any theory of stereopsis that requires eye movements.     

Exposure-time and spatial-frequency effects in the tilt illusion

The exposure durations of a vertical test line and a tilted inducing grating were varied and the tilt illusion thus generated was found to change as a function of this variation. Significant direct effects (acute-angle expansion) and indirect effects (acute-angle contraction) were found to occur at times consistent with Andrew's estimate of the time course of inhibition in the visual system when the inducing grating had a spatial frequency of 10 cycles deg-1. However, a 2.71 cycles deg-1 grating gave significant effects at exposure durations of 10 as well as 1000 ms, while in a further experiment a 10.91 cycles deg-1 grating gave significant effects at 1000 ms only. These results seem to suggest that orientation interactions thought to be due to inhibition (direct effect) and disinhibition (indirect effect) may occur within both sustained and transient channels with concomitant differences in time constants.     

On the theoretical error bound for estimating psychometric functions

The theoretical limits to the amount of error, or the Cramer-Rao bounds, were derived for estimating psychometric functions. These theoretical error bounds were compared with the variability of psychometric functions estimated from human as well as computer-simulated observers. For the simulated observers, due to the limited efficiency of the sampling strategies, including the placement of the signals and the distribution of the trials, the variances of the estimated parameters are seven times the theoretical bound for threshold and 22 times that for slope. For the human observers, the variance is 18 times the theoretical bounds for threshold and 80 times that for slope. Therefore, a major portion of the variances (60% for threshold and 73% for slope) for the human observers is associated with factors other than sampling strategies. Further improvement of the accuracy for estimating psychometric functions will depend on not only optimizing the sampling strategy, but also better understanding the various sources of error related to the behavior of human observers.     

Spatial frequency and the detection of temporal discontinuity in superimposed and adjacent gratings

The properties of the detecting mechanism involved in the resolution of temporal discontinuities of visually presented stimuli have been investigated in two experiments. In Experiment 1, observers made judgments of discontinuity when superimposed presentations of sine-wave gratings of 1, 3, 6, and 10 cycles/deg were presented for either a 20- or a 200-msec duration per presentation at a contrast of .1 and .4. Threshold separation for discontinuity detection indicated a linear increase as spatial frequency increased, with a lesser effect for longer duration exposure and higher contrast. Experiment 2 involved adjacent presentation of the second grating, and a small linear decrease in separation threshold as a function of increasing spatial frequency occurred. The effect of spatial frequency on temporal discontinuity detection is dependent on whether the second stimulus is superimposed or adjacent.     

Monaural and binaural temporal integration of noise bursts

Summary A comparison was made between monaural and binaural temporal integration of noise bursts at threshold. The data indicate partial integration, with approximately a 6 dB decrease in threshold per decade increase in noise burst duration for both conditions of stimulation (i.e., parallel functions) for durations ranging from 4 to 256 msec. When thresholds in dB are plotted as a function of log duration, the linear component accounts for 99% of the data indicating no essential change in the partial integration functions up to at least 256 msec. The intercept difference between the monaural and binaural integration functions is 2.5 dB.     

Mapping the zone of eye-height utility for seated and standing observers

In a series of experiments, we delimited a region within the vertical axis of space in which eye height (EH) information is used maximally to scale object heights, referred to as the "zone of eye height utility" (Wraga, 1999b Journal of Experimental Psychology, Human Perception and Performance 25 518-530). To test the lower limit of the zone, linear perspective (on the floor) was varied via introduction of a false perspective (FP) gradient while all sources of EH information except linear perspective were held constant. For seated (experiment 1a) observers, the FP gradient produced overestimations of height for rectangular objects up to 0.15 EH tall. This value was taken to be just outside the lower limit of the zone. This finding was replicated in a virtual environment, for both seated (experiment 1b) and standing (experiment 2) observers. For the upper limit of the zone, EH information itself was manipulated by lowering observers' center of projection in a virtual scene. Lowering the effective EH of standing (experiment 3) and seated (experiment 4) observers produced corresponding overestimations of height for objects up to about 2.5 EH. This zone of approximately 0.20-2.5 EH suggests that the human visual system weights size information differentially, depending on its efficacy.     

Postural control in otolith disorders

It was the aim of the present paper to investigate the influence of otolith disorders on human postural control by different methods. The 33 patients of our study had undergone a minor head injury and suffered subsequently from an utricular or sacculo-utricular disorder as evidenced by vestibular evoked myogenic potential recordings and eccentric rotation recordings of the otolith-ocular responses. Postural control was assessed by performing stance/gait tests (standard balance deficit test, SBDT) and by evaluating trunk sway (using angular velocity sensors). Moreover, classical tests of the posterior column of the spinal tract (Romberg/Unterberger) and the dynamic posturography (sensory organization test, SOT) were included. It could be shown that SBDT tasks with reduced proprioceptive and visual cues (e.g. standing on foam, eyes closed) are most sensitive for an otolith disorder. The patients showed an increased trunk sway in the pitch plane (i.e. linear motion as adequate utricular stimulus) and an increase in sway velocities (i.e. tilting movements as adequate saccular stimulus) compared to controls. The SOT was most sensitive for combined (sacculo-utricular) otolith disorders (78%) while vestibulospinal tests are not enough sensitive. In essence, otolith disorders evidently impair human postural control and have been possibly underestimated as a source of posttraumatic postural imbalance as yet.     

Simulated angular head oscillation enhances vection in depth

Research has shown that adding simulated linear head oscillation to radial optic flow displays enhances the illusion of self-motion in depth (ie linear vection). We examined whether this oscillation advantage for vection was due to either the added motion parallax or retinal slip generated by insufficient compensatory eye movement during display oscillation. We constructed radial flow displays which simulated 1 Hz horizontal linear head oscillation (generates motion parallax) or angular head oscillation in yaw (generates no motion parallax). We found that adding simulated angular or linear head oscillation to radial flow increased the strength of linear vection in depth. Neither type of simulated head oscillation significantly reduced vection onset latencies relative to pure radial flow. Simultaneous eye-movement recordings showed that slow-phase ocular following responses (OFRs) were induced in both linear and angular viewpoint oscillation conditions. Vection strength was significantly reduced by active central fixation when viewing displays which simulated angular, but not linear, head oscillation. When these displays with angular oscillation were viewed without stable fixation, vection strength was found to increase with the velocity and regularity of the OFR. We conclude that vection improvements observed during central viewing of displays with angular viewpoint oscillation depend on the generation of eye movements.     

The identification of the direction of electrocutaneous stimulation along lineal multistimulator arrays

Three experiments were conducted in an effort to evaluate the ability of observers to identify the direction of brief-duration spatiotemporal patterns applied to the skin. In Experiment 1, observers were required to identify the direction of linear sweeps of electrical stimulation having varying total durations (sweep durations). Performance was evaluated at several loci on the body. The effects of stimulator number and spacing on the identification of sweep direction were evaluated in Experiment 2. In Experiment 3, the effects of temporal sequencing of stimuli on the “apparent movement” phenomenon were evaluated at two body loci: the forearm and the abdomen. The results from all three experiments suggest that the ability to identify the direction of spatiotemporal sweeps can be heavily influenced by body locus, number, and spacing of electrodes. In short, the design of the tactile display may have important ramifications to the success of any sensory substitution transform hardware.     

Psychometric functions for the discrimination of differences in intensity of gaussian noise

A new theory of sensory functioning by Laming predicts how the shape of the psychometric function depends on the context in which a signal is presented. The discrimination of intensities of noise was therefore studied with four different stimulus configurations. In one, observers discriminated between two separate noise samples that differed in intensity. In accordance with the theory, a normal probability integral provided a better fit to each observer's data than either of two other functions: a normal integral with respect to the square of the difference, or a normal integral with respect to the fourth power of the difference. In a second task, observers detected an increment in a continuous noise. For eight out of nine sets of data, a square-law function provided a better fit than either a normal integral or fourth-power function. A third task asked observers to decide which of two noises was amplitude modulated. The predicted square-law function provided the best fit for four out of five observers. In a fourth task, one observer detected an interval of amplitude modulation in a continuous noise. As predicted by the theory, a fourth-power function provided the best fit. In addition, Weber fractions for difference discriminations decreased approximately with the square root of sample duration for durations up to 300 msec, whereas Weber fractions for increment detections decreased approximately directly with duration for durations up to 100 msec. The results are usually in qualitative agreement with the theory and often in quantitative agreement as well.     

Pattern and orientation effects on afterimage duration

Patterns composed of a pair of lines: vertical + horizontal, vertical + oblique, horizontal + oblique, and oblique + oblique, either centrally-aligned or edge-aligned, were shown at two positions of rotation. After a 1-s exposure to the pattern observers timed the duration of afterimages consisting of individual lines (fragmentary state) and the pattern as a whole (unitary state) for the ensuring 60 s. Summing unitary and fragmentary afterimage durations yielded the total afterimage duration for each pattern. Three hypotheses were confirmed by the results: (i) total afterimage duration is constant for all patterns when integrated spatiotemporal luminances are equal; (ii) unitary afterimage duration is also constant; (iii) fragmentary afterimages of vertically oriented lines have longer durations than either their horizontal or oblique pair members, regardless of alignment and, with one exception, rotation. For all patterns, the durations of the unitary and the fragmentary state represent a fixed portion of the total afterimage duration. The difference between afterimage duration for differently oriented lines in patterns which include a vertical is discussed in relation to the vertical-horizontal illusion, the function and structure of cortical orientation processes, and perceptual development.     

On the time course of perceptual information that results from a brief visual presentation.

A briefly presented visual stimulus engenders an available-information function that lags behind the physical stimulus. We report two experiments that focus on the iconic-decay portion of this function, which falls to 0 over a 200-300 ms period following stimulus offset. In each experiment, to-be-reported digit strings were shown for varying durations followed by a noise mask at varying poststimulus intervals. We found the shape of the performance curve relating digit-report probability to stimulus exposure duration to be independent of stimulus-mask interstimulus interval. This finding is consistent with the proposition that the iconic-decay function's shape is independent of stimulus duration and allows us to identify this shape. We rejected exponential iconic decay for 6 of 8 observers; however, all observers' decay functions could be adequately fit by gamma decay, a generalization of exponential decay.     

Waldo reveals cultural differences in return fixations

ABSTRACT

Humans routinely perform visual search towards targets to adapt to the environment. These sequences of ballistic eye movements are shaped by a combination of top–down and bottom–up factors. Recent research documented that human observers display cultural-specific fixation patterns in a range of visual processing tasks. In particular, eye movement strategies extracting information from faces clearly differs between Western Caucasian (WC) and East Asian (EA) observers. However, whether such cultural differences are also present for visual scene processing remains debated. To this aim, we recorded the eye movements of WC and EA observers while they were solving visual search problems parametrically varying in difficulty: Where’s Waldo. Both groups had a comparable familiarity with the Waldo books reaching a comparable level of accuracy in target detection. Both cultural groups also showed a comparable temporal effect on inhibition of return, with longer fixation durations when saccades were performed to a return location compared to other locations. Westerners, however, located Waldo faster than Easterners. Interestingly, this modulation of speed was likely related to differences occurring on the low-level mechanisms of spatial inhibition of return, with EA observers returning more often to previously visited locations than the WC observers. This suboptimal eye movement strategy in the Easterners might be engendered by their cultural perceptual bias consisting in? a greater use of extra-foveal information. Overall, our data point towards the existence of a subtle, but significant difference in the processing of visual scenes across observers from different cultures during active visual search.     

The relation between horizontality and rod-and-frame and vestibular navigational performance

Sex differences on Piaget's water-level (horizontality) test are well established but poorly understood. In this article, correlates of female horizontality performance are systematically explored. Across the five experiments reported, it was found that female subjects who failed the water-level test (poor-horizontality female subjects) were selectively impaired on tasks that required processing information from the otolith organs. In Experiment 1, poor-horizontality female subjects were found to be impaired relative to good-horizontality subjects on the rod-and-frame test. In Experiment 2, a relation was found between female horizontality performance and the ability to process vestibular information in a passive transport task. Experiment 3 ruled out poor spatial updating as a mediating factor in this relation. The results of Experiments 4 and 5 indicated that poor-horizontality female subjects perform randomly on vestibular navigation because they cannot judge linear displacement under conditions of passive transport. The linear transport task is similar to the rod-and-frame task in that both require the central processing of otolith signals. It is proposed that one way to solve the water-level test is to imagine, on the basis of prior perceptual experiences, what the water level looks like inside tilted containers. Because of complex visual-otolith interactions, poor-horizontality female subjects may experience these events differently than good-horizontality subjects.     

Applicability of the parallel-clock model to duration discrimination

The parallel-clock model assumes that when an observer is presented with two durations in succession, the total subjective duration (corresponding to the sum of first and second durations) and the second duration are each accumulated in a separate sensory register. In dealing with some relation between the two durations, the observer compares the difference between the contents of the two registers with the contents of the second register. With the further assumption that the psychophysical power law is valid for the continuum of time, the model has previously been shown to account well for duration scaling data. After adapting the model in the vein of Thurstone for duration discrimination data, it was tried out on such data gathered by Allan (1977) from 13 observers. With chi-square as the examined statistic, (1) five distributions were compared and the normal one chosen, (2) one categorization model, three choice models, and two linear regression models were compared with the 3-parameter version of the parallel-lock model, which proved superior, and (3) a 4–5-parameter version of the parallel-clock model, assuming a discontinuity in the psychophysical function, was shown to yield an excellent fit in terms of the Kolmogorov-Smirnov statistic.     

Brief exposure to contingent reinforcement produces a sustained increment in the strength of an elicited response.

Squirrel monkeys' lever pressing produced by response-independent shock was measured before, and for an extended period following, exposure to a shock-avoidance procedure. Following avoidance training, the frequency of responding increased by multiples of 10 to 50 across subjects and evidence little or no decrement for up to 6 months of postreinforcement testing. Manual responding produced by intense environmental stimulation may be substantially strengthened by a brief history of reinforcement, such that it is sustained over long periods without reinforcement.     

Sensitivity of early human vision to 3-D orientation in line-drawings.

The modern "textbook" view of visual perception contains an inherent paradox. On the one hand, it claims that relatively simple edge-extraction processes requires a stimulus exposure of approximately 50 ms. On the other hand, it says that the identification of objects in photographs and line-drawings can be highly accurate with exposure durations as short as 100 ms. It is tempting to conclude that all the difficult work of perception occurs in the 50 ms that elapse between when these two tasks are accomplished. This article argues against this view, suggesting instead that much more than edge-extraction is accomplished by the early visual processes. To illustrate this view, a computational model is described that is capable of recovering the 3-D orientation of objects from some line-drawings, rapidly and in parallel. Data from recent visual search experiments with human observers are presented in support of this model and the implications of this view for the "textbook" view are discussed.     

Mental-state attribution drives rapid, reflexive gaze following

When presented with a face stimulus whose gaze is diverted, observers’ attention shifts to locations fixated by the face. Such “gaze following” has been characterized by some previous studies as a consequence of sophisticated theory of mind processes, but by others (particularly those employing the “gaze-cuing” paradigm) as an involuntary response that is triggered directly and reflexively by the physical features of a face. To address this apparent contradiction, we modified the gaze-cuing paradigm using a deception procedure to convince observers that prerecorded videos of an experimenter making head turns and wearing mirrored goggles were a “live” video link to an adjacent room. In two experiments, reflexive gaze following was found when observers believed that the model was wearing transparent goggles and could see, but it was significantly reduced when they believed that the experimenter wore opaque goggles and could not see. These results indicate that the attribution of the mental state “seeing” to a face plays a role in controlling even reflexive gaze following.