Perceived warmth and skin temperature as functions of the duration and level of thermal irradiation!

This study examined the correlations among the degree of perceived warmth. the level and duration of irradiant flux. and the thermal response of the skin. For any constant duration. perceived warmth grew as a power function of the difference between the irradiant flux of the stimulus and the flux that approximates the absolute threshold for warmth. The exponent of the power function was about 0.87 for the shortest durations (2—6 sec). but rose to 1.04 for the longest duration of exposure (12 sec). For any constant level of flux. perceived warmth changed only slightly with duration. In contrast, superficial skin temperature. and inferred temperatures of deeper layers of the skin, rose continuously and markedly with duration. Neither the change in tissue temperature. nor the rate of change of tissue temperature, nor thermal gradient correlated consistently with level of perceived warmth. The change in the difference between the temperature 0.2 mm and that 1.0 mm below the skin surface provided a fairly good but not perfect correlate to perceived warmth. The findings suggest the possibility that sensory adaptation at the site of the receptor system mediating warmth could act in such a way as nearly to offset the effect of rising skin temperature with increased duration ofstimulation.     

Perceived duration as a function of pitch

It was demonstrated with 7 observers that the duration of a high frequency tone was perceived to be longer than the duration of a low frequency tone, even though the actual duration of the two tones was equal.     

Brightness and loudness as functions of stimulus duration

The brightness of white light and the loudness of white noise were measured by magnitude estimation for sets of stimuli that varied in intensity and duration. Brightness and loudness both grow as power functions of duration up to a critical duration, beyond which apparent magnitude is essentially independent of duration. For brightness, the critical duration decreases with increasing intensity, but for loudness the critical duration is nearly constant at about 150 msec. Loudness and brightness also grow as power functions of intensity. The loudness exponent is the same for all durations, but the brightness exponent is about half again as large for short durations as for long. The psychophysical power functions were used to generate equal-loudness and equal-brightness functions, which specify the combinations of intensity E and duration T that produce the same apparent magnitude. Below the critical duration ET equals k for equal brightness, and ET^a equals k for equal loudness. The value a is about 0.7 for threshold and about 1.25 for supraliminal loudness.     

Brightness and loudness as functions of stimulus duration

The brightness of white light and the loudness of white noise were measured by magnitude estimation for sets of stimuli that varied in intensity and duration. Brightness and loudness both grow as power functions of duration up to a critical duration, beyond which apparent magnitude is essentially independent of duration. For brightness, the critical duration decreases with increasing intensity, but for loudness the critical duration is nearly constant at about 150 msec. Loudness and brightness also grow as power functions of intensity. The loudness exponent is the same for all durations, but the brightness exponent is about half again as large for short durations as for long. The psychophysical power functions were used to generate equal-loudness and equal-brightness functions, which specify the combinations of intensity E and duration T that produce the same apparent magnitude. Below the critical duration ET equals k for equal brightness, and ET^a equa Is k for equal loudness. The value a is about 0.7 for threshold and about 1.25 for supraliminal loudness.     

Perceived duration of expected and unexpected stimuli

Three experiments assessed whether perceived stimulus duration depends on whether participants process an expected or an unexpected visual stimulus. Participants compared the duration of a constant standard stimulus with a variable comparison stimulus. Changes in expectancy were induced by presenting one type of comparison more frequently than another type. Experiment 1 used standard durations of 100 and 400 ms, and Experiments 2 and 3 durations of 400 and 800 ms. Stimulus frequency did not affect perceived duration in Experiment 1. In Experiments 2 and 3, however, frequent comparisons were perceived as shorter than infrequent ones, and discrimination performance was better for infrequent comparisons. Overall, this study supports the notion that infrequent stimuli increase the speed of an internal pacemaker.     

Perceived brightness as a function of flash duration in the peripheral visual field

Using a method of direct magnitude estimation, perceived brightness was measured in the dark-adapted eye with brief flashes of varying duration (1–1,000 msec), size (16’–116’), and retinal loci (0°–60°) for the lower photopic luminance levels covering the range between 8.60 and 86 cd/m² in steps of .5 log units. Perceived brightness increased as a function of flash duration as well as luminance up to approximately 100 msec, then remained constant above 100 msec. The enhancement of brightness at about a 50-msec flash duration has been observed not in the fovea but in the periphery. Target size also has been found to be effective on brightness.     

Measuring consciousness: task accuracy and awareness as sigmoid functions of stimulus duration

When consciousness is examined using subjective ratings, the extent to which processing is conscious or unconscious is often estimated by calculating task performance at the subjective threshold or by calculating the correlation between accuracy and awareness. However, both these methods have certain limitations. In the present article, we propose describing task accuracy and awareness as functions of stimulus intensity (thus obtaining an accuracy and an awareness curve) as suggested by Koch and Preuschoff (2007). The estimated lag between the curves describes how much stimulus intensity must increase for awareness to change proportionally as much as accuracy and the slopes of the curves are used to assess how fast accuracy and awareness increases and whether awareness is dichotomous. The method is successfully employed to assess consciousness characteristics on data from four different awareness scales.     

Perceived duration,visual persistence,and neural integration

Varying stimulus intensity while measuring the perceived duration/visual persistence of brief light flashes has yielded disparate results. Some studies have found a direct relationship between the two variables; others have found an inverse relationship. Several models have been suggested to unify this behavioral literature. They invoke the absolute intensity and the nature of the judgment as explanatory variables. We now present physiological data whose analysis was motivated by these models. We measured the duration of photoreceptor potentials as a function of light intensity and response measure. One response measure was. the length of time required for the response to decline from the peak by a criterion amount. The other response measure was the length of time a response stayed above a criterion level. These data suggest that each behaviorally based model captured a different aspect of a single underlying mechanism and that a melding of the two critical concepts would harmonize all of the results: In this melding, the sensory signals that mediate visual perception would have the type of complex intensity- and time-dependent properties found in real neural responses.     

On additivity of duration reproduction functions

In the present paper properties of theoretical response functions in the duration reproduction task (drt) are studied. If the drt response is to be interpreted as the measure of a temporal duration elapsed in the past, the reproduction function (rf) must be additively measuring. The additivity property is defined for bivariate rfs, taking into account the delay between retention and reproduction. The requirement that an rf be additively measuring leads to a system of two functional equations, which are solved by (i) linear functions of time, or (ii) functions of the form yielded by the ‘dual klepsydra model’ of duration reproduction [Wackermann, J., & Ehm, W. (2006). The klepsydra model of internal time representation and time reproduction. Journal of Theoretical Biology, 239, 482-493]. This result supports the outstanding rôle of the ‘klepsydraic reproduction function’ (krf) in models of internal representation and reproduction of temporal durations.     

The effects of mental imagery on skin temperature and skin temperature sensation

In a series of six experimental sessions five subjects were instructed to imagine their hand in a hot and cold water stream. During the imagery period the subjects estimated with a psychophysical scale their subjective temperature sensations caused by the imagery. Skin temperature was measured from the thumb of the subjects' dominant hand. After each session the subjects were asked whether they had succeeded in producing an imagery. The skin temperature changes deviated significantly from the control level in the successful imagery experiments. Differences in the skin temperature changes between the successful and unsuccessful imagery experiments were significant. The skin temperature changes measured and the subjects' temperature sensations, produced by the imagery, were similar in the successful imagery experiments. The possible relationships between mental imagery and changes in skin temperature and skin temperature sensation are discussed.