Effects of fixed-time shocks and brief stimuli on food-maintained behavior of rats

When a fixed-time schedule of shocks was presented to rats lever pressing for food on a random-interval schedule, a pattern of behavior developed with a high rate of pressing after shock declining to near zero before the next shock was delivered. Once this pattern had stabilized, one-quarter of the shocks were replaced with brief auditory stimuli (tones) in a random sequence. Tone maintained behavior similar to shock, although tone was never paired with shock. Both tone and shocks elicited responding when presented at various times as probe stimuli, and responding was usually totally suppressed if neither stimulus occurred at the beginning of the fixed-time interval. When other stimuli were paired with tone and shock, only those paired with tone gained discriminative control and elicited responding. These findings suggest that stimuli that signal a shock-free, or safe, period will maintain the pattern of behavior generated by shock on a fixed-time schedule. There is a parallel between this phenomenon and the control of behavior on second-order schedules of positive reinforcement with nonpaired brief stimuli.     

Modulation of the acoustic startle reflex in humans in the absence of anticipatory changes in the middle ear reflex

If a weak tone precedes an intense tone, then the acoustic startle eyeblink reflex elicited by the stronger stimulus is inhibited. It has been suggested that the leading stimulus gives rise to a protective middle ear reflex that attenuates the effective intensity of the second. This hypothesis was tested and disproved. In seven subjects intense tone bursts sufficient to elicit both intratympanic and eyeblink responses were presented sometimes alone and sometimes preceded at various lead times (25 to 400 msec) by a weak tone. The weak tone inhibited the amplitude of the eye blink to the strong tone, maximally at intervals of 100 to 200 msec, but was never seen to produce any of the anticipatory impedance changes that would be characteristic of middle ear reflex activity during the interval between the two stimuli.     

Modification of the human blink reflex by transient and sustained features of acoustic prestimulation

The effects of acoustic stimuli whose onsets and durations were controlled to vary their transient and sustained features on the size of a subsequently elicited blink reflex were examined in humans. Prestimuli both with and without transient features inhibited the reflex when they preceded the eliciting stimulus by brief lead intervals, showing that acoustic transients are sufficient, but not necessary, for reflex inhibition. Inhibition evoked by transient and sustained stimulus features showed partial summation, and inhibition evoked by stimuli with only transient and with transient and sustained features showed similar decay functions with increasing lead intervals. Blink augmentation was found at longer lead intervals early but not late in a session, and was more evident in women than men. Prestimuli with only transient features were more effective than those with both transient and sustained features, showing that sustained stimulus energy at the time of reflex elicitation is not only not necessary for blink augmentation, but also diminishes it.     

Spectral frequency and the modulation of the acoustic startle reflex by background noise

The rat's (Long-Evans) acoustic startle reflex to a high-frequency tone burst (10.5 kHz) was depressed by intense high-frequency band-pass noise (8-16 kHz) but enhanced by low frequency noise (1-2 kHz). However, contrary to the hypothesis that the depression of startle in intense background noise is produced by sensory masking, the reflex to a low-frequency tone burst (at 1 kHz) was depressed by both high- and low-frequency band-pass noise. Two additional hypotheses are offered to supplement sensory masking in order to explain the asymmetry in these data. The first is that the intratympanic reflex, which acts as a high pass filter on acoustic input, is elicited in intense backgrounds. The second is that acoustic startle reflexes elicited by intense low-frequency tones are in part elicited by their high-frequency distortion products and that these distortion products are then masked by high-frequency background noise.     

Modality-repetition and attentional effects on reflex blinking in infants and adults

The ability of a brief prepulse to inhibit reflexively elicited startle is a robust phenomenon in adults of several species but is weak or absent in infants. The possibility that afferent processing of the prepulse is inadequate in infants was tested by assessing the integrity of two other types of reflex modulation that occur in modality-specific paths, that is, attenuation by repetition of same-modality stimuli and enhancement by modality-selective attention. The reflex, measured by electromyographic activity of the muscle controlling blink, was elicited by intense light flashes or noise bursts preceded by brief acoustic or visual prepulses and delivered during attention-directing acoustic or visual foregrounds that evoked cardiac deceleration. Modality-repetition effects were evidenced by smaller peak blink magnitude and longer latency of blinking to same than to different modality pairs and did not differ as a function of age (4-month-old infants or college students). Attention effects were also seen in both infants and adults and, in accord with previous findings, were evident in magnitude for infants and latency for adults. Thus, immaturity in paths mediating these effects could not explain delayed development of prepulse inhibition. Other possibilities include delayed maturation of extrinsic inhibition or of transient-processing systems.     

Acoustic augmentation and inhibition of the human eyeblink

The human eyeblink elicited by a mechanically produced tap to the glabella was inhibited by a mild acoustic stimulus presented 200 msec prior to the tap and was augmented when the same acoustic stimulus was presented simultaneously with the tap. Monaural presentation of the acoustic stimulus prior to the tap yielded more reflex inhibition than when that same stimulus was presented binaurally. Binaural presentation of the acoustic stimulus simultaneously with the tap yielded more reflex augmentation than when that same stimulus was presented monaurally. These findings lend credence to the proposition that reflex inhibition and reflex augmentation are mediated by separate neural pathways.     

Similar effects of attention directed to acoustic and tactile stimuli on prepulse inhibition of acoustic startle

Prepulse inhibition (PPI) is assumed to index automatic and controlled processing. In three experiments (n= 32, 22, and 30) participants were asked to judge the duration of a prepulse in comparison with a stimulus presented 4000 ms before the prepulse. A distracter was presented simultaneously with the prepulse to increase the cognitive demands of the task. PPI was assessed at stimulus onset asynchronies (SOAs) of 30-150 ms, and 420 ms. The prepulse was either a tone (60 dB) or a tactile stimulus (21 kPa), and startle was elicited by 95 dB white noise. Directing attention to the prepulse increased PPI at SOAs of 60 ms and longer in all experiments, but the sensory modality to which attention was directed played only a minor role. We conclude that directing attention to both acoustic and tactile prepulses increased PPI.     

Inhibition of the cutaneous eyeblink reflex by unilateral and bilateral acoustic input: the persistence of contralateral antagonism in auditory processing

The eyeblink reflex elicited by a cutaneous stimulus is inhibited by weak auditory stimuli that are heard just before the blink. It has been shown that monaural prestimuli produce more reflex depression than binaural prestimuli do, suggesting that reflex modification is sensitive to the outcome of antagonistic connections between contralateral auditory inputs. We examined the time course of this antagonism by giving unilateral versus bilateral pairs of noise pips 100 msec before the reflex eyeblink, with the noise pips separated by 0, 1, 4, or 8 msec. Unilateral stimuli were more effective in every condition, but their advantage diminished with increased delay between the two components. The extended bilateral and unilateral trends of increasing reflex depression with increased delay meet at about 15 msec; if this extrapolation is valid, 15 msec represents the upper limit on this system's retention of the location of a brief noise impulse. The rate of convergence of the two temporal functions reflects the decay of the antagonistic effect of one noise on its contralateral counterpart.     

Visual form integration and discontinuity detection

Two experiments were conducted to determine if discontinuity detection limits the visual integration of two stimuli presented successively. If this is the case, then presenting two dim stimuli should permit better integration than presenting two bright stimuli. In Experiment 1, five observers named the position of the missing dot in a 5 x 5 dot matrix. Twelve randomly selected dots were presented in each of two stimulus presentations. The stimuli varied in intensity in a ratio of 15:1 and stimulus onset asynchrony (SOA) varied between 50 msec and 80 msec. At the longer SOAs, presenting two bright stimuli led to a higher percentage of correct responses than presenting two dim stimuli. There was no difference between those conditions at the shorter SOAs. In Experiment 2, 12 naive observers rated the amount of integration of the same stimuli on a 7-point scale, under the same presentation conditions. Rated integration was higher with two dim stimuli than with two bright stimuli. These apparently contradictory results are explained in terms of Hawkins and Shulman's distinction between two kinds of visual persistence. It is concluded that subjects can respond to integration and discontinuity detection separately. No evidence was found that discontinuity detection limits the integration.     

Second-order schedules with paired auditory brief stimuli

Pigeons were exposed to multiple second-order schedules of paired and unpaired brief stimuli in which responding on the main key was reinforced according to a fixed-interval thirty-second schedule by a brief stimulus (a tone in the paired schedule) and advancement to the next segment of the second-order schedule. In Experiment 1, a response on the second key was required during the tone in its fourth and final presentation to produce food. Responses during earlier brief stimuli indicated the extent to which the final brief stimulus was discriminated from preceding ones. Responding was comparable during all tones, extending prior findings with visual paired brief stimuli and weakening explanations of subjects' failure to discriminate between brief-stimulus presentations in terms of elicited responding. In Experiment 2 the number of fixed-interval segments comprising the second-order schedules varied from one through eight. Although main-key response rates increased across segments in both experiments, they increased much less sharply with a variable number of segments. These results suggest that the increase in main-key response rates across segments is due primarily to a degree of temporal discrimination not reflected on the second key. Main-key response rates were higher on paired auditory brief-stimulus schedules than on unpaired visual brief-stimulus schedules, especially in Experiment 2, thus further extending findings with visual brief stimuli to second-order schedules with auditory brief stimuli.     

Reflex modification by acoustic signals in newborn infants and in adults

This research asked whether the reflexive eyeblink elicited by a tap to the glabella (the flat region of skin between the eyebrows) is modified by acoustic signals which either precede or accompany the tap. Five experiments employing identical reflex modification procedures on neonates and adults suggest developmental differences in processing auditory stimuli. Neonates failed to exhibit reflex inhibition by either prior acoustic or tactile stimuli. Adults exhibited robust reflex inhibition to these same stimuli. Neonates, however, exhibited reliable reflex augmentation when mild (70 dB re: 0.0002 dyne/cm2) tones were presented simultaneously with the tap. For adults, tone intensities of at least 90 dB were necessary to obtain reliable reflex augmentation. The developmental processes implied by these findings are discussed.     

Acceleration and suppression of rats' responding to avoid foot shock and tail shock

Signalled response-independent shocks were superimposed on rats' wheel-turn responding to avoid shock administered to their feet through a grid floor or to their tails through fixed electrodes. In Experiment I, a tone paired with response-independent foot shock increased responding in three of four rats; a tone paired with tail shock increased responding in only one of four rats and suppressed responding in two rats. In Experiment II, a tone presented randomly with respect to response-independent shock had no reliable effect on responding to avoid foot shock or tail shock. In Experiment III, tail shock and foot shock were compared in a within-subject design while the temporal pattern of responding during conditioned stimuli was recorded. Responding during the conditioned stimulus preceding foot shock was characterized by initial suppression of responding at tone onset, followed by increased responding just before response-independent shock. Responding was suppressed throughout the conditioned stimulus preceding tail shock. Foot shock elicited bursts of responding, but tail shock did not.     

Task-irrelevant sounds influence both temporal order and apparent-motion judgments about tactile stimuli applied to crossed and uncrossed hands

It has been suggested that judgments about the temporal–spatial order of successive tactile stimuli depend on the perceived direction of apparent motion between them. Here we manipulated tactile apparent-motion percepts by presenting a brief, task-irrelevant auditory stimulus temporally in-between pairs of tactile stimuli. The tactile stimuli were applied one to each hand, with varying stimulus onset asynchronies (SOAs). Participants reported the location of the first stimulus (temporal order judgments: TOJs) while adopting both crossed and uncrossed hand postures, so we could scrutinize skin-based, anatomical, and external reference frames. With crossed hands, the sound improved TOJ performance at short (≤300 ms) and at long (>300 ms) SOAs. When the hands were uncrossed, the sound induced a decrease in TOJ performance, but only at short SOAs. A second experiment confirmed that the auditory stimulus indeed modulated tactile apparent motion perception under these conditions. Perceived apparent motion directions were more ambiguous with crossed than with uncrossed hands, probably indicating competing spatial codes in the crossed posture. However, irrespective of posture, the additional sound tended to impair potentially anatomically coded motion direction discrimination at a short SOA of 80 ms, but it significantly enhanced externally coded apparent motion perception at a long SOA of 500 ms. Anatomically coded motion signals imply incorrect TOJ responses with crossed hands, but correct responses when the hands are uncrossed; externally coded motion signals always point toward the correct TOJ response. Thus, taken together, these results suggest that apparent-motion signals are likely taken into account when tactile temporal–spatial information is reconstructed.

     

Prepulse effects on magnitude estimation of startle-eliciting stimuli and startle responses

The present studies investigated the relationship between prepulse effects on the modification of the brainstem startle reflex and magnitude estimates of startle-eliciting stimuli. In Experiment 1, startle eyeblink responses were elicited in 24 students, half of whom were instructed to estimate the loudness of the startle stimulus (actual intensities of 80, 90, and 100 dB) and half of whom were instructed to estimate the magnitude of their eyeblink. When weak acoustic prepulses preceded the startle-eliciting stimulus, eyeblink amplitude was inhibited, and estimates of response magnitude decreased, but estimates of startle stimulus magnitude decreased only when 100-dB startle stimuli were presented. In Experiment 2, the same startle stimuli were preceded on some trials by a vibrotactile prepulse to the hand. In conditions in which startle amplitude was inhibited, startle stimulus magnitude estimates were not affected. This suggests that the effect of acoustic prepulses on 100-dB startle stimuli in Experiment 1 may have been due to loudness assimilation, an effect independent of the prepulse inhibition of startle responding.     

Temporal summation and reaction time to double-light pulses at suprathreshold levels

Temporal summation of the visual system was studied at suprathreshold levels by measuring reaction time (RT) to the double pulses that were equal in luminance (L) and duration. The RTs were determined as functions of L and the stimulus onset asynchrony (SOA) between the onsets of the two pulses. The relation between RT and L obtained for a given SOA was found to be a power function with the exponent 1/3. The function relating L to SOA was then derived for each of three criterion RTs. The L-SOA relationship indicated partial summation at SOAs shorter than about 20 msec. Inhibition was observed at SOAs longer than about 80 msec. These findings were consistent with the predictions from a temporal integration model.     

Microgenesis as traced by the transient paired-forms paradigm

Two successive, spatially overlapping human faces were exposed for recognition with SOAs ranging from 20 to 160 msec. The subjects effectively perceived one face, which at short SOAs mostly resembled the first stimulus and with increasing SOAs gradually shifted towards the appearance of the second, dimmer stimulus. These results replicated those from the study by Calis, et al, and extended them to the experimental conditions of controlled simultaneity of each of the two temporally separate, extremely brief stimuli and to the conditions of personally unfamiliar stimulus-subjects. In the second experiment we employed a direct measurement of the microgenetic focus in real time by using a procedure by which the subjects' judgments about the relative temporal order of the critical visual stimulus and an auditory click were recorded. Via this procedure it was shown that one of the effects of the first visual stimulus is to speed up the microgenetic process for the second stimulus which then appears subjectively earlier as compared to the single-stimulus control.     

Conditioned reinforcement and discrimination in second-order schedules

Pigeons were exposed to multiple second-order schedules in which responding on the “main key” was reinforced according to either a variable-interval or fixed-interval schedule by production of a brief stimulus on the “brief-stimulus key”. A response was required to the brief stimulus during its fourth (final) presentation to produce food; responses to the earlier brief stimuli indicated the extent to which the final brief stimulus was discriminated from preceding ones. Main-key response rates were higher in early components of paired brief-stimulus schedules, in which each brief stimulus was the same as that paired with reinforcement, than in comparable unpaired brief-stimulus or tandem schedules. Poor discrimination occurred between paired brief stimuli (Experiment I). When chain stimuli on the main key induced a discrimination between the first two and second two brief stimuli, the response-rate enhancement in the paired brief-stimulus schedule persisted (Experiment II). Rate enhancement diminished when the initial link of the chain included the first three components (Experiment IV). Eliminating the contingency between responding and brief-stimulus production also diminished rate enhancement (Experiment III). The results show that the discriminative and conditioned reinforcing effects of food-paired brief stimuli may be selectively manipulated and suggest that the reinforcing effects are modulated by other reinforcers in the situation.     

Failure to develop a conditional reflex by stimulation of the cephalad portion of the severed vagosympathetic trunk: Its significance in terms of the central connections of the vagus

Stimulation of the central stump of either vagosympathetic trunk in the dog, the contralateral nerve remaining intact, regularly provoked deep respiratory movements with forceful expiration, followed by a period of apnea, and a fall in blood pressure, systolic and diastolic, of 20–60 mm/Hg. Stimulation of the cephalad portion of the left nerve provoked brief acceleration of heart rate during the period of hyperventilation, followed by bradycardia; when the stimulus was applied to the central stump of the right nerve heart rate remained relatively unchanged. When a 12-second tone as a conditional stimulus (CS) was reinforced during its last six seconds with such stimulation of the vagosympathetic trunk as an unconditional stimulus (US), despite the striking visceromotor responses elicited by the US, no conditional reflex was established even after more than 3,400 trials in 16 dogs (34–781 trials per animal).     

Temporal integration and vibrotactile backward masking

Subjects were presented with vibrotactile target patterns to their left index fingertips. The target patterns varied in the number of line segments that they contained and were presented in the presence or absence of a backward-masking stimulus. The stimulus onset asynchrony (SOA) between the target and masker was varied. In an identification task, subjects' errors indicated that the effect of the masker at brief SOAs was to increase the perceived number of line segments in the target. This effect diminished with increasing SOA, and at the longest SOAs subjects confused targets with patterns containing the same number of line segments but varying in how the line segments were related. In an estimation task, the effect of the masker was to increase the number of line segments estimated to be contained in the target pattern. The effect of the masker at brief SOAs is discussed in terms of an integration theory of vibrotactile backward masking. At longer SOAs, the results suggest that the masker may interfere with the extraction of relational information in the target pattern.     

多感觉整合的时间再校准

跨通道刺激的时间同步性是多感觉整合的必要条件, 但是由于刺激物理传导与神经传导的差异, 它们在时间上并非完全匹配。时间再校准指大脑能够适应跨通道刺激间很短的时间延迟的现象, 反映了多感觉整合在时间维度上的可塑性, 表现为适应相继呈现的跨通道刺激后, 主观同时点向时间延迟方向的偏移。本文主要介绍了时间再校准的通道效应与潜在机制, 其初始加工阶段, 它与刺激内容加工的关系及主要的影响因素。今后的研究应当进一步探索时间再校准能否发生于早期加工阶段, 检验其认知过程是否具有双向性, 探讨空间选择性注意的作用, 并结合神经机制的研究, 从综合的视角进行更完善的理论建构。