Biomedical subjects

Peter Heil

Publications and source records attributed to Peter Heil.

6 recordsLinked to original sources

PubMed2006

Correcting for false alarms in a simple reaction time task.

Simple reaction times (RTs) constitute an important source of information and tool in human and animal psychophysics, in cognitive neuroscience, and in the clinic. We measure simple RTs to auditory stimuli, in a high signal rate vigilance design, to examine the possibility that simple RT may be used as a tool to study mechanisms of temporal summation at absolute threshold. By means of catch trials, we monitor the subjects' tendencies to produce false alarms, that is reactions not controlled by the reaction stimulus. Here we examine the possibility that a model of a race between a stimulus-controlled reaction process and a false alarm process can account for the numbers as well as for the timing of early and late RTs on stimulus trials in our experiments. We show that the responses in both tails of our empirical RT distributions on stimulus trials are indeed correctly predicted by the race model and can be considered false alarms. This suggests that the race model might also provide a reasonable description of the way in which false alarms and stimulus-controlled reactions combine when they overlap in time. We examine the magnitudes of the estimated effects of false alarms on several parameters of the RT distributions by application of the race model. The analyses reveal that the effects not only vary with false alarm rate but also with stimulus parameters. Our data suggest that the race model may provide a theoretically reasonable and easy means of correcting for false alarms in simple RT paradigms and thus may constitute a useful alternative to the common practice of truncation.

Adult↗

PubMed2006

Comparison of absolute thresholds derived from an adaptive forced-choice procedure and from reaction probabilities and reaction times in a simple reaction time paradigm.

An understanding of the auditory system's operation requires knowledge of the mechanisms underlying thresholds. In this work we compare detection thresholds obtained with a three-interval-three-alternative forced-choice paradigm with reaction thresholds extracted from both reaction probabilities (RP) and reaction times (RT) in a simple RT paradigm from the same listeners under otherwise nearly identical experimental conditions. Detection thresholds, RP, and RT to auditory stimuli exhibited substantial variation from session to session. Most of the intersession variation in RP and RT could be accounted for by intersession variation in a listener's absolute sensitivity. The reaction thresholds extracted from RP were very similar, if not identical, to those extracted from RT. On the other hand, reaction thresholds were always higher than detection thresholds. The difference between the two thresholds can be considered as the additional amount of evidence required by each listener to react to a stimulus in an unforced design on top of that necessary for detection in the forced-choice design. This difference is inversely related to the listener's probability of producing false alarms. We found that RT, once corrected for some irreducible minimum RT, reflects the time at which a given stimulus reaches the listener's reaction threshold. This suggests that the relationships between simple RT and loudness (reported in the literature) are probably caused by a tight relationship between temporal summation at threshold and temporal summation of loudness.

Adult↗

PubMed2004

Towards a unifying basis of auditory thresholds: the effects of hearing loss on temporal integration reconsidered.

For signal detection and identification, the auditory system needs to integrate sound over time. It is frequently assumed that the quantity ultimately integrated is sound intensity and that the integrator is located centrally. However, we have recently shown that absolute thresholds are much better specified as the temporal integral of the pressure envelope than of intensity, and we proposed that the integrator resides in the auditory pathway's first synapse. We also suggested a physiologically plausible mechanism for its operation, which was ultimately derived from the specific rate of temporal integration, i.e., the decrease of threshold sound pressure levels with increasing duration. In listeners with sensorineural hearing losses, that rate seems reduced, but it is not fully understood why. Here we propose that in such listeners there may be an elevation in the baseline above which sound pressure is effective in driving the system, in addition to a reduction in sensitivity. We test this simple model using thresholds of cats to stimuli of differently shaped temporal envelopes and durations obtained before and after hearing loss. We show that thresholds, specified as the temporal integral of the effective pressure envelope, i.e., the envelope of the pressure exceeding the elevated baseline, behave almost exactly as the lower thresholds, specified as the temporal integral of the total pressure envelope before hearing loss. Thus, the mechanism of temporal integration is likely unchanged after hearing loss, but the effective portion of the stimulus is. Our model constitutes a successful alternative to the model currently favored to account for altered temporal integration in listeners with sensorineural hearing losses, viz., reduced peripheral compression. Our model does not seem to be at variance with physiological observations and it also qualitatively accounts for a number of phenomena observed in such listeners with suprathreshold stimuli.

Animals↗

PubMed2004

First-spike latency of auditory neurons revisited.

The timing of the first, and sometimes only, spike of auditory neurons evoked by an acoustic stimulus depends on a variety of parameters. Recent studies have suggested that several of these dependencies originate from processes in the first synapse of the auditory system and that first-spike timing is further modified by central processing. The variation of first-spike latency with stimulus parameters contains considerable information about those parameters, as recently explored in several sensory systems. Codes based on the relative timing of first spikes in ensembles of neurons appear to be easily decodable, energetically efficient, reliable, and fast.

Action Potentials↗

PubMed2003

A unifying basis of auditory thresholds based on temporal summation.

Thresholds of auditory-nerve (AN) fibers and auditory neurons are commonly specified in terms of sound pressure only, implying that they are independent of time. At the perceptual level, however, the sound pressure required for detection decreases with increasing stimulus duration, suggesting that the auditory system integrates sound over time. The quantity commonly believed to be integrated is sound intensity, implying that the auditory system would have an energy threshold. However, leaky integrators of intensity with time constants of hundreds of milliseconds are required to fit the data. Such time constants are unknown in physiology and are also incompatible with the high temporal resolution of the auditory system, creating the resolution-integration paradox. Here we demonstrate that cortical and perceptual responses are based on integration of the pressure envelope of the sound, as we have previously shown for AN fibers, rather than on intensity. The functions relating the pressure envelope integration thresholds and time for AN fibers, cortical neurons, and perception in the same species (cat), as well as for perception in many different vertebrate species, are remarkably similar. They are well described by a power law that resolves the resolution-integration paradox. The data argue for the integrator to be located in the first synapse in the auditory pathway and we discuss its mode of operation.

Animals↗

PubMed2002

Auditory activation of "visual" cortical areas in the blind mole rat (Spalax ehrenbergi).

The mole rat (Spalax ehrenbergi) is a subterranean rodent whose adaptations to its fossorial life include an extremely reduced peripheral visual system and an auditory system suited for the perception of vibratory stimuli. We have previously shown that in this blind rodent the dorsal lateral geniculate nucleus, the primary visual thalamic nucleus of sighted mammals, is activated by auditory stimuli. In this report we focus on the manifestation of this cross-modal compensation at the cortical level. Cyto- and myeloarchitectural analyses of the occipital area showed that despite the almost total blindness of the mole rat this area has retained the organization of a typical mammalian primary visual cortex. Application of the metabolic marker 2-deoxyglucose and electrophysiological recording of evoked field potentials and single-unit activity disclosed that a considerable part of this area is activated by auditory stimuli. Previous neuronal tracing studies had revealed the origin of the bulk of this auditory input to be the dorsal lateral geniculate nucleus which itself receives auditory input from the inferior colliculus.

Acoustic Stimulation↗