Changes In Stimulus Parameters Research Articles

Cognitive function and brain activation before and after transcutaneous cervical vagus nerve stimulation in healthy adults: A concurrent tcVNS-fMRI study.

Transcutaneous vagus nerve stimulation, which involves the application of electrical currents to the cervical (tcVNS) or auricular (taVNS) branches of the vagus nerve, may be a potential treatment for improving cognitive dysfunction. taVNS may improve cognitive performance in healthy adults, and fewer studies have been performed on the effects of tcVNS on cognition in healthy subjects. We conducted a randomized, single-blind, crossover-controlled trial to investigate the effects of tcVNS stimulation on cognitive function and neural activity in the brains of healthy adults. This study provides support for further tcVNS studies for the treatment of cognitive impairment. Twenty-one participants were randomly divided into two groups, A and B. Group A received tcVNS first and then sham-tcVNS, while group B received the intervention in the reverse order, receiving sham stimulation first and then true stimulation. All subjects were required to perform cognitive function tests before and after receiving intervention, and functional magnetic resonance imaging (fMRI) was performed concurrently during the intervention. We hypothesized that tcVNS would have an effect on the cognitive performance of the subjects and alter the neural activity of the brain. The present study showed that tcVNS had beneficial effects on cognitive performance, mainly improving memory and language skills and attention. tcVNS intervention produced significant spontaneous neural activity in the calcarine gyrus, fusiform gyrus, lingual gyrus, and parahippocampal gyrus of the brain. Future tcVNS/fMRI trials will need to explore the effects of changes in stimulus parameters on the neural activity response of the brain.

Angular tuning of tilt illusion depends on stimulus duration

In the tilt illusion, the orientation of a central stimulus appears tilted away from a surrounding stimulus when angular difference is between 0 deg and 50 deg. Studies have repeatedly shown that the tilt illusion exhibits the strongest effect with the angular difference around 15 deg and this angular tuning is robust to various changes in stimulus parameters. We revisited the well-reported angular tuning of the tilt illusion, in relation to the recently-reported modulation of illusion magnitude by stimulus duration. We examined the tilt illusion with a wide range of stimulus duration (10–640 ms) and angular difference (7.5–75.0 deg). The results confirmed that the peak magnitude of the tilt illusion increased with shorter durations. However, we also found that the position of the peak shifted to larger angular differences with shorter durations. Evidently, the angular tuning profile of the tilt illusion is not fixed but can change with stimulus duration. The peak shift may be explained if orientation-selective lateral inhibition responsible for the tilt illusion sharpens its tuning over time.

Double-blind optimization of subcallosal cingulate deep brain stimulation for treatment-resistant depression: a pilot study

Deep brain stimulation (DBS) of the subcallosal cingulate (SCC) is reported to be a safe and effective new treatment for treatment-resistant depression (TRD). However, the optimal electrical stimulation parameters are unknown and generally selected by trial and error. This pilot study investigated the relationship between stimulus parameters and clinical effects in SCC-DBS treatment for TRD. Four patients with TRD underwent SCC-DBS surgery. In a double-blind stimulus optimization phase, frequency and pulse widths were randomly altered weekly, and corresponding changes in mood and depression were evaluated using a visual analogue scale (VAS) and the 17-item Hamilton Rating Scale for Depression (HAM-D-17). In the open-label postoptimization phase, depressive symptoms were evaluated biweekly for 6 months to determine long-term clinical outcomes. Longer pulse widths (270-450 μs) were associated with reductions in HAM-D-17 scores in 3 patients and maximal happy mood VAS responses in all 4 patients. Only 1 patient showed acute clinical or mood effects from changing the stimulation frequency. After 6 months of open-label therapy, 2 patients responded and 1 patient partially responded. Limitations include small sample size, weekly changes in stimulus parameters, and fixed-order and carry-forward effects. Longer pulse width stimulation may have a role in stimulus optimization for SCC-DBS in TRD. Longer pulse durations produce larger apparent current spread, suggesting that we do not yet know the optimal target or stimulus parameters for this therapy. Investigations using different stimulus parameters are required before embarking on large-scale randomized sham-controlled trials.

Direct electrical stimulation of the somatosensory cortex in humans using electrocorticography electrodes: a qualitative and quantitative report

Objective. Recently, electrocorticography-based brain–computer interfaces have been successfully used to translate cortical activity into control signals for external devices. However, the utility of such devices would be greatly enhanced by somatosensory feedback. Direct stimulation of somatosensory cortex evokes sensory perceptions, and is thus a promising option for closing the loop. Before this can be implemented in humans it is necessary to evaluate how changes in stimulus parameters are perceived and the extent to which they can be discriminated. Approach. Electrical stimulation was delivered to the somatosensory cortex of human subjects implanted with electrocorticography grids. Subjects were asked to discriminate between stimuli of different frequency and amplitude as well as to report the qualitative sensations elicited by the stimulation. Main results. In this study we show that in humans implanted with electrocorticography grids, variations in the amplitude or frequency of cortical electrical stimulation produce graded variations in percepts. Subjects were able to reliably distinguish between different stimuli. Significance. These results indicate that direct cortical stimulation is a feasible option for sensory feedback with brain–computer interface devices.

A novel physiological mechanism for pitch encoding in monkey primary auditory cortex.

Pitch is a fundamental perceptual attribute of hearing. While auditory cortex is implicated in pitch perception, how pitch is represented at the cortical level remains unclear. The present study examines a novel hypothesis for how the pitch of pure tones and of harmonic complex tones, with or without the fundamental frequency, is encoded in primary auditory cortex (A1): pitch is represented non‐topographically by the temporal distribution of population activity in A1. Sounds of lower pitch evoke a greater proportion of sustained multiunit activity (MUA), relative to initial onset MUA, than sounds of higher pitch, such that the temporal distribution of MUA systematically varies with pitch. Pure tones and harmonic complexes with the same pitch evoke a similar proportion of sustained MUA. The temporal distribution of MUA is largely invariant to changes in stimulus parameters (e.g., level and relative phase) that leave the perceived pitch unchanged. Timing of AEP components recorded in superficial layers of A1 parallels similar pitch‐related changes in AEPs recorded in humans. Coding of perceptual qualities based on the time course of neural activity has been proposed in other sensory modalities (e.g., olfaction) and offers a novel alternative to topographic representations of pitch at the cortical level.

The effect of background noise on P300 to suprathreshold stimuli

Both the amplitude and latency of P300 vary with changes in stimulus parameters. Stimuli at intensities or pitch separations near threshold evoke a smaller and later P300. P300 is also affected by extraneous stimulus parameters in tasks where stimulus frequency separation is large and stimuli are well above intensity thresholds. For example, the presence of background white noise when tones are suprathreshold and easily detectable has been reported to increase P300 latency. However, the effects of background masking noise on P300 amplitude and scalp topography have not been reported. Subjects performed an oddball task both in the presence and in the absence of background noise. Performance accuracy was unaffected by background noise. P300 showed latency increases when noise was present, but P300 peak amplitude was unaffected. P300 scalp topography was stable across both conditions. P300 latency is affected by background noise, even when performance is not, but amplitude and amplitude topography remain unaffected.

Human Cortical Areas Underlying the Perception of Optic Flow: Brain Imaging Studies

In summary, we have reviewed electrophysiological and brain imaging studies of motion and optic-flow processing. Single-unit studies indicate that MST (V5a) is a site of optic-flow extraction and that this information can be used to guide pursuit eye movements and to estimate heading. The EEG and MEG studies point to a localized electrical dipole in occipitotemporal cortex evoked by visual motion. We have also discussed the evidence from functional imaging studies for response specificity of the rCBF and BOLD effects in posterior cortex to visual motion and optic flow. Focal attention modulates the amplitude of the BOLD signal evoked by visual motion stimulation. Retinotopic mapping techniques have been used to locate region borders within the visual cortex. Our results indicate that striate (V1) and extrastriate areas (V2, V3/V3a) respond robustly to optic flow. However, with exception of a more pronounced response in V3/V3a to random walk, we found little evidence for response selectivity with respect to flow type and disparity in these early visual areas. In a similar fashion, the human V5/V5a complex responds well to optic flow, but these responses do not vary significantly with the type of flow field and do not seem to depend on disparity. In contrast, the kinetic occipital area (KO/V3b) responds well to optic-flow information, and it is the only area that produces more pronounced activation to the disparity in the flow fields. These initial results are promising because they suggest that the fMRI method can be sensitive to changes in stimulus parameters that define flow fields. More work will be required to explore the extent to which these responses reflect the neuronal processing of optic flow. Eye position tracking is now possible during fMRI experiments. We have demonstrated that the eye movements affect the BOLD responses in motion-sensitive areas (Kimming et al., 1999). Further experiments in our laboratory are aimed at understanding the effects of eye movements on the neuronal coding of complex optic-flow fields (Schira et al., 1999).

Short communication: mapping of somatosensory cortices with functional magnetic resonance imaging in anaesthetized macaque monkeys.

Functional magnetic resonance imaging (fMRI) in macaque monkeys is emerging as a potent candidate to bridge the gap between data from human fMRI studies and data from anatomy, electrophysiology and lesion studies in monkeys. The primary (SI) and secondary (SII) somatosensory cortices are the principal regions for somatosensory information processing and contain systematic representations of the body surface map (somatotopy). To examine the functional organization of the somatosensory cortices in anaesthetized macaque monkeys with fMRI, we asked whether focal and differential activation could be observed in SI and SII in response to tactile stimulation with two parameters: body sides (right and left) and body regions (hand and face). We found that changes in stimulus parameters elicited differential focal activation in both SI and SII in two ways. First, the hand and face stimulation activated SI and SII in the contralateral, but not in the ipsilateral, hemisphere. Second, the hand and face stimulation differentially activated two adjacent regions in both SI and SII. These fMRI results appear to correlate with previous mapping studies by other methods in the macaque somatosensory cortices. This study shows the feasibility of fMRI studies in mapping multiple sensory areas in monkeys by which we can distinguish between adjacent functionally distinct regions.

Effects of Neonatal Exposure to Nicotine on Electrophysiological Parameters in Adult Rats

In clinical studies and animal models, there is evidence that nicotine exposure during gestation can result in deficits in cognitive performance. The present study examined the effects of two doses of neonatal nicotine exposure on adult brain activity as assessed by the N1 and P3 components of the event-related potential (ERP) and background electroencephalography (EEG). Nicotine (0 mg, 1 mg/kg/day, 4 mg/kg/day) was administered to neonatal rat pups from postnatal day 4 (PN4) through PN12 with an artificial rearing paradigm; suckled rats served as additional control subjects. Nicotine exposure was specifically found to alter responses of the P3 component of the ERP, recorded in dorsal hippocampus, to changes in stimulus parameters. A significant reduction in the response of the P3A component to the noise tone as compared with the level of the frequently presented tone was found. A significant reduction in the response to the noise tone as compared with the level of the infrequently presented tone also was seen in the P3B component. No effects of drug exposure were found on the N1 component in any lead, although artificial rearing produced specific effects on the latency of the N1 component in cortex. No significant differences among treatment groups were found on any of the EEG-dependent variables. Female rats overall were found to have significantly higher EEG amplitudes than the males, a finding previously reported in our laboratory. However, no overall effects of gender were found on any ERP component. These studies suggest that neonatal nicotine exposure specifically reduces the electrophysiological response of the hippocampus to changes in auditory stimuli. Additional studies will be necessary to link these P3 amplitude changes to the effects of nicotine on the developing brain in human and animal subjects.

Encoding of amplitude modulation in the peripheral auditory system

Auditory-nerve fibers synchronize to the envelope of SAM stimuli over a wide range of modulation parameters. Synchronization is found at all characteristic frequencies and shows moderate gain differences between fibers of different spontaneous rate. Modulation transfer functions are uniformly low pass, with an upper frequency limit that systematically increases with characteristic frequency. As expected, envelope phase locking in bushy cells of the anteroventral cochlear nucleus is nervelike, but marked transformations occur in other cell classes. Phase-locking gain is very high in onset cells in posteroventral cochlear nucleus. High gains are also seen in the dorsal cochlear nucleus; however, small changes in stimulus parameters often result in large changes in gain and phase. In general, it is unclear whether high gains are functionally significant, or rather a mere reflection of the transient response properties of cells. There is evidence for the latter in one class of high-gain cell. Effects of modulation on average rate are small in the auditory nerve, but can be large in cochlear nucleus and, with binaural stimulation, in the olivary complex. The lateral superior olive and its bushy cell afferents provide an example of a circuit in which temporal envelope information is converted into average rate changes. [Work supported by NIDCD.]

Tectal codification of eye movements in goldfish studied by electrical microstimulation

This work compares the tectal codification of eye movements in goldfish with those reported for other vertebrate groups. Focal electrical stimulation was applied in various tectal zones and the characteristics of evoked eye movements were examined as a function of (i) the position of the stimulation over the tectal surface, (ii) the initial position of the eyes and (iii) the parameters (pulse rate, current strength, duration) of the stimulus. In a large medial zone, stimulation within the intermediate and deep layers of the tectum evoked contraversive saccades of both eyes, whose direction and amplitude were roughly congruent with the retinotopic representation of the visual world within overlying layers. These saccades were minimally influenced by the initial position of the eye in the orbit. The topographical arrangement of evoked saccades and body movements suggests that this tectal zone triggers orienting responses in a similar way to those described in other vertebrates. Stimulations applied within the caudal tectum also evoked contraversive saccades, but—in disagreement with the overlying retinotopic map—the vertical component was absent. Taken together with electrically evoked body movements reported in free-swimming fish, these saccades could reveal that this zone is involved in escape responses. When stimulations were applied within the anteromedial zone of the tectum, contraversive movements of both eyes appeared much more dependent on initial eye position. Saccades elicited from this area displayed characteristics of “goal-directed saccades” which were similar to those described in the cat. The generation of goal-directed movements from the anteromedial zone suggests that this portion of the goldfish optic tectum has a different intrinsic organization or is connected with the brainstem saccade generator in a different fashion than the medial zone. Finally, stimulation of the extreme anteromedial zone evoked convergent eye movements. These movements and those reported in free-swimming fish following electrical stimulation of this tectal area suggest that this zone could be involved in feeding responses. The relationships between the parameters of electrical stimulation and the characteristics of elicited saccades suggest that the stimulated location within the tectum determines a constant direction in the evoked saccade, whereas the amount and duration of tectal activity, as mimicked by changes in stimulus parameters, together with the tectal locus, determine the velocity and amplitude of the evoked saccade.

Linear and non-linear components in the centre-surround response of X- and Y-cells in the cat lateral geniculate nucleus

Thalamocortical projection cells of cat dorsal lateral geniculate nucleus (dLGN) have been described to exhibit different types of non-linear integration of spatial contrast in addition to the linear integration inside their classical receptive field (CRF). We analysed whether a single mechanism might generate the two harmonic distortions of a linear response elicited inside the CRF and the shift effect elicited from regions outside the CRF. Therefore, both non-linear response types were investigated with identical stimulus conditions in the same cell. A quantitative analysis revealed that both response types can be elicited in nearly all Y-cells and in at least 50% of the X-cells. With blockade of GABAA inhibition by bicuculline methiodide (BICU) the number of X-cells with shift effect (SE) and second harmonics (2H) increased to more than 80%. Both, SE and 2H exhibited significantly correlated variations in their response-amplitude and -latency and in the frequency of their occurrence with changes in stimulus parameters (contrast, spatial frequency, area) and during BICU application. We assume that both non-linear contrast responses, the SE and the 2H might depend on the same (most probably retinal) mechanisms. We further suggest that the principal organisation of X- and Y-cell receptive fields might be very similar and that the differing spatial contrast responses may result from the different spatial resolution of their CRF subunits.

Long-latency event-related potentials in rats: Effects of task and stimulus parameters

Animal models of event-related potentials have recently been developed in rats in order to gain further understanding of the psychobiological variables which underlie these waveforms. In the present study, unanesthetized male Wistar rats, chronically implanted with electrodes, were utilized in order to: (i) compare event-related potentials recorded following the presentation of passively presented auditory stimuli from different neocortical, hippocampal and perihippocampal sites; (ii) test the effects of changes in stimulus probability and loudness on event-related potentials recorded from those sites; and (iii) record event-related potentials from rats who were actively performing in a tone discrimination task. The results of these studies showed that in all electrode sites (frontal cortex, parietal cortex, entorhinal cortex, hippocampus) a series of large amplitude potentials in the 10–200 ms latency range could be recorded in response to passively presented stimuli. Late positive potentials in the 300–400 ms range were only identified in recordings from the posterior cortex, entorhinal area, and dorsal hippocampus. Some of these late positive components were also found to be sensitive to changes in stimulus probability. A similar series of waves were detected in a paradigm where rats were required to actively discriminate between two tones; however, the morphologies of the waveforms were found to be more distinct. These studies suggest that rats may be good subjects for the exploration of the neural origins of event-related potentials. These studies demonstrate that rats performing in an auditory discrimination task can generate electrophysiological potentials which are time locked to the onset of a “cognitively relevant” stimulus (event-related potentials). These potentials can be recorded in limbic (hippocampus and amygdala) and cortical (parietal cortex) brain sites. The event-related potentials recorded in rats respond to changes in stimulus parameters in a similar fashion to those previously described in monkeys and human subjects. The identification of a rat model of event-related potentials provides an opportunity to further explore the neural origins of event-related potentials, to estimate the role of genetics in determining individual variation in waveforms, as well as to provide electrophysiological assays of the effects of various drugs on neurosensory and cognitive processing.

Long latency event related potentials in rats: The effects of changes in stimulus parameters and neurochemical lesions

Animal models of event related potentials (ERPs) have recently been developed in order to gain further understanding of the psychobiological variables which may underlie these brain potentials. In the present study, unanaesthetized rats were utilized in order to evaluate the effects on rat ERP morphology of changes in the auditory stimulus parameters used to elicit these potentials such as tone probability and intensity. In addition, the consequences of reductions in norepinephrine (NE) produced by six-hydroxydopamine (6-OHDA) lesions to the area of the dorsal noradrenergic bundle in ERP wave forms were evaluated. Forty, experimentally naive, male rats chronically implanted with electrodes were used in this study. The results of these studies showed that in all electrode sites (frontal cortex, ventral thalamus, dorsal hippocampus, locus coeruleus) a series of large amplitude potentials in the 10-200 msec latency range could be recorded, some of which were sensitive to changes in the auditory stimulus parameters such as probability and tone intensity. Late positive potentials in the 300-400 msec range could be identified in recordings from the dorsal hippocampus and were found to be sensitive to probability independent of tone intensity. Dorsal noradrenergic bundle lesions were also found to produce significant changes in these rat ERP components. Lesioned animals were found to have increases in amplitude to the early negative potentials (in the 50-100 msec range) in response to frequent tones in cortical leads and decreases in the amplitude of the late positive potentials (in the 300-400 msec range) recorded in hippocampal leads in response to infrequent tones. These findings are consistent with a role for NE in the forebrain in the processing of novel or "selective" stimuli.

An examination of VEP response phase

The accuracy of phase sensitive signal detection (PSD) as applied to swept visual evoked potential retrieval depends upon phase stability. If large phase shifts over occur the course of a swept run, amplitude will be lost in any one PSD channel and threshold estimation may be inaccurate. We were able to demonstrate large latency shifts in the conventional computer averaged VEP and phase shifts in the Fourier-analyzed steady-state VEP, as a function of contrast and spatial frequency. However, the phase changes observed over that portion of a sweep where there is a visually driven response are much smaller than obtained from averaged VEPs to a series of fixed stimulus values. The difference between the observed phase shifts may be caused by a delay in phase response when stimuli are swept. This hypothesis was supported by the finding that the phase of the steady-state VEP response requires from 1 to 2 sec to stabilize following a change in contrast. Sweeping contrast or spatial frequency results in a physiologically different response than when averaged VEP responses are measured to discrete changes in stimulus parameters.

The two-dimensional spatial structure of simple receptive fields in cat striate cortex.

1. A reverse correlation (6, 8, 25, 35) method is developed that allows quantitative determination of visual receptive-field structure in two spatial dimensions. This method is applied to simple cells in the cat striate cortex. 2. It is demonstrated that the reverse correlation method yields results with several desirable properties, including convergence and reproducibility independent of modest changes in stimulus parameters. 3. In contrast to results obtained with moving stimuli, we find that the bright and dark excitatory subregions in simple receptive fields do not overlap to any great extent. This difference in results may be attributed to confounding the independent variables space and time when using moving stimuli. 4. All simple receptive fields have subregions that vary smoothly in all directions in space. There are no sharp transitions either between excitatory subregions or between subregions and the area surrounding the receptive field. 5. Simple receptive fields vary both in the number of subregions observed, in the elongation of each subregion, and in the overall elongation of the field. In contrast with results obtained using moving stimuli, we find that subregions within a given receptive field need not be the same length. 6. The hypothesis that simple receptive fields can be modeled as either even symmetric or odd symmetric about a central axis is evaluated. This hypothesis is found to be false in general. Most simple receptive fields are neither even symmetric nor odd symmetric. 7. The hypothesis that simple receptive fields can be modeled as the product of a width response profile and an orthogonal length response profile (Cartesian separability) is evaluated. This hypothesis is found to be true for only approximately 50% of the cells in our sample.

Repetitive firing in layer V neurons from cat neocortex in vitro

Input-output relations of large neurons from layer V of cat sensorimotor cortex were studied in an in vitro slice preparation using steps and ramps of intracellularly injected current. Depolarization attained during the interspike interval (ISI) was compared to the voltage levels required to activate a previously described (29) persistent sodium current (INaP). INaP was studied using a single-electrode voltage clamp in the same cells tested for firing behavior. Following an injected current step, firing rate declined smoothly to a steady level with a time course that was approximately exponential in most cells (tau, 9-43 ms). In most cells, the relation between firing rate and injected current (f-I relation) consisted of two linear segments, both for adapted, steady firing and for early intervals during adaptation. The slope of the steeper, initial (or sole) linear segment of the f-I curve averaged 26.2 Hz/nA during steady firing and was steeper when plotted for early interspike intervals. The variation of the depolarization at which spike initiation occurred (firing level) and the membrane potential between rhythmic spikes was examined during adaptation and steady firing. In most cells, firing level rose rapidly during a rhythmic train to a steady value. The steady firing level attained remained unchanged over a wide range of steady firing rates. Nevertheless, the mean depolarization during the interspike interval (V) increased approximately linearly with steady firing rate. Even at the slowest firing rates, V is sufficient to activate INaP. The use of injected current ramps demonstrated that neocortical cells were sensitive to rate of change of stimulus current (dI/dt) as well as its amplitude (I). The use of ramps followed by steady currents demonstrated that the repetitive response lagged behind changes in stimulus parameters and did not reach a steady state even during slow ramps; i.e., the response depended on time as well as on I and dI/dt. Instantaneous firing rate during the ramp increased linearly with time for a wide range of ramp slopes (dI/dt). The instantaneous firing rate of early interspike intervals was also linearly related to ramp slope for small ramp slopes. In spite of these linear relationships, quantitative analysis indicated that firing rate during ramp stimulation cannot, in general, be described by a simple linear combination of separate amplitude- and rate-dependent terms. The repetitive firing properties of the in vitro neurons are compared to those of in vivo neocortical neurons and other cell types.(ABSTRACT TRUNCATED AT 400 WORDS)

Detection and discrimination of small, brief lights: Variable tuning of opponent channels

There is disagreement as to how closely the properties of the pathways that detect small spots resemble the properties of the achromatic system. Spectral sensitivities for small, brief lights show a single, relatively broadband peak similar to the achromatic spectral sensitivity. The lights also appear relatively desaturated near threshold. However, recent field sensitivity data (Finkelstein and Hood, 1981, 1982) have shown that opponent mechanisms are either directly involved in detecting small spots, or they interact with, and desensitize, a strictly achromatic detection pathway. The test sensitivity, test mixture and wavelength discrimination data of the present study support the first alternative; they implicate opponent (chromatic) mechanisms in the detection of small, brief lights. However, the data cannot be fit by the same opponent systems used to fit large-test data. They suggest instead an hypothesis in which large and small lights are detected by opponent mechanisms that change their spectral tuning with changes in stimulus parameters.

The 'late' reflex responses to muscle stretch: the 'resonance hypothesis' versus the 'long-loop hypothesis'.

1. Experiments were performed to check the validity of previous claims concerning the ;long-loop' aetiology of ;late' reflex electromyogram (e.m.g.) responses to muscle stretch in man. The primary aim was to investigate whether observations previously presented in favour of the ;long-loop hypothesis' are explicable also in terms of the ;resonance hypothesis', according to which the ;late' reflex components represent spinal, short-latency responses to intramuscular oscillations initiated by the impact.2. The contracting wrist flexors of healthy subjects were exposed to trains of recurrent 25-50 Hz stretch stimuli (wrist torque pulses). Each of the initial two or three pulses in the train was followed by e.m.g. peaks with a latency of 20-25 msec. The e.m.g. peaks driven in this way had the following characteristics in common with the successive two or three e.m.g. peaks which were induced by single ramp stretches or tendon taps. (a) Changes in stimulus parameters which altered the strength of the initial e.m.g. peak often had an opposite effect on the strength of the succeeding peak(s). Muscle vibration which attenuated the initial peak often enchanced the succeeding one(s). (b) The initial e.m.g. peak was less affected than the succeeding peak(s) by the subjects' attempts to respond with rapid ;resist' or ;let go' reactions.3. Intramuscular oscillations (monitored by a needle accelerometer) and e.m.g. responses evoked by single ramp stretches and/or tendon taps were also studied in the long thumb flexor, the calf muscles and the masseter muscle. In the thumb flexor, the initial accelerometer deflexion was only rarely succeeded by a short latency e.m.g. peak, but the succeeding wave in the needle accelerogram was followed by such a peak, appearing about 40 msec after stimulus application. By contrast, the calf muscles and the jaw elevators exhibited a high amplitude, short-latency e.m.g. response to the first but only rarely to the second intramuscular oscillation wave.4. The interval between initial and second e.m.g. peaks following tendon taps was longer for calf muscles than for wrist flexors and longer for wrist flexors than for jaw elevators. Similar differences were observed with respect to the intervals between the damped intramuscular oscillations initiated by the impacts.5. Without denying the existence of ;long-loop reflexes' it is concluded that the characteristics of the ;late' reflex responses to muscle stretch in man are explicable also in terms of the ;resonance hypothesis'.

Attention and saccadic eye movements.

Four threshold detection experiments addressed three issues concerning the relationship between movements of spatial attention and saccadic eye movements: (a) the time course of attention shifts wit saccades, (b) the response of the two systems to changes in stimulus parameters, and (c) the relationship of attention to saccadic suppression. These issues bear on the more general question of the degree of independence between the saccadic and attentional movement systems. The results of these experiments support the contention that the mechanisms that shift attention are separate from those that control saccadic eye movements. Relevant events in the visual field periphery, however, will trigger both a saccade and attention shift. The attentional response to such events does not appear to be under subjects' control. The implication of these results for theories of saccadic suppression is discussed.