Search

The visuomotor mental rotation (VMR) of a saccade requires a response to a region of space that is dissociated from a stimulus by a pre-specified angle, and work has shown a monotonic increase in reaction times as a function of increasing oblique angles of rotation. These results have been taken as evidence of a continuous process of rotation and have generated competing hypotheses. One hypothesis asserts that rotation is mediated via frontoparietal structures, whereas a second states that a continuous shift in the activity of direction-specific neurons in the superior colliculus (SC) supports rotation. Research to date, however, has not examined the neural mechanisms underlying VMR saccades and both hypotheses therefore remain untested. The present study measured the behavioural data and event-related brain potentials (ERP) of standard (i.e., 0° of rotation) and VMR saccades involving 35°, 70° and 105° of rotation. Behavioural results showed that participants adhered to task-based rotation demands and ERP findings showed that the amplitude of the contingent negative variation (CNV) linearly decreased with increasing angle of rotation. The cortical generators of the CNV are linked to frontoparietal structures supporting movement preparation. Although our ERP design does not allow us to exclude a possible role of the SC in the rotation of a VMR saccade, they do demonstrate that such actions are supported by a continuous and cortically based rotation process.

Executive function is transiently improved (i.e., 2peak test to determine cardiorespiratory fitness and estimated lactate threshold (LT), followed by separate 10-min sessions of light- (i.e., 25 W), moderate- (i.e., 80% estimated LT), and heavy-intensity (i.e., 15% of the difference between LT and V̇O2peak) aerobic exercise. An estimate of CBF during exercise was achieved via transcranial Doppler ultrasound and near-infrared spectroscopy to quantify blood velocity (BV) through the middle cerebral artery and deoxygenated hemoglobin (HHb), respectively. Executive function was assessed before and after each session via the executive-mediated antisaccade task (i.e., saccade mirror-symmetrical to a target). Results demonstrated that BV increased in relation to increasing exercise intensity, whereas HHb decreased by a comparable magnitude independent of intensity. In terms of executive function, null hypothesis and equivalence tests indicated a comparable magnitude postexercise reduction in antisaccade reaction time across exercise intensities. Accordingly, the magnitude of CBF change during exercise does not impact the magnitude of a postexercise executive function benefit.

Energy storage requirements and its management are important considerations for dc microgrid designs that have a high penetration of stochastic distributed sources and loads. Modern control methods, such as Hamiltonian Surface Shaping and Power Flow Control (HSSPFC), often rely on a reduced order model of the microgrid for controller design. This paper explores (1) the reduced order boost converter model for use in development of advanced control schemes via a detailed, switching mode model implemented on a Typhoon HIL 602 with a controller-in-the-loop (CIL) and (2) a design methodology that may be used for determining converter distributed storage requirements for the closed loop controls.

Perceptual judgments related to stimulus-sets are represented computationally different than individual items. In particular, the perceptual averaging hypothesis contends that the visual system represents target properties (e.g., eccentricity) via a statistical summary of the individual targets included within a stimulus-set. Here we sought to determine whether perceptual averaging governs the visual information mediating an oculomotor task requiring top-down control (i.e., antisaccade). To that end, participants completed antisaccades (i.e., saccade mirror-symmetrical to a target) – and complementary prosaccades (i.e., saccade to veridical target location) – to different target eccentricities (10.5°, 15.5° and 20.5°) located left and right of a common fixation. Importantly, trials were completed in blocks wherein eccentricities were presented with equal frequency (i.e., control condition) and when the ‘proximal’ (10.5°: i.e., proximal-weighting condition) and ‘distal’ (20.5°: i.e., distal-weighting condition) targets were respectively presented five times as often as the other eccentricities. If antisaccades are governed by a statistical summary then amplitudes should be biased in the direction of the most frequently presented target within a block. As expected, pro- and antisaccade across each target eccentricity were associated with an undershooting bias and prosaccades were refractory to the manipulation of target frequency. Most notably, antisaccades in the proximal-weighting condition had a larger undershooting bias than the control condition, whereas the converse was true for the distal-weighing condition; that is, antisaccades were biased in the direction of the most frequently presented target. Thus, we propose that perceptual averaging extends to motor tasks requiring top-down cognitive control.

The goal of the present investigation was to test the somatosensory processing model's (SPM) assertion that tactile actions and perceptions are mediated via egocentric and allocentric frames of reference, respectively (Dijkerman & de Hann's 2007: Behavioral and Brain Sciences). To accomplish that objective, Experiment 1 required that participants use their right hand to grasp and manually estimate differently sized objects placed on the forearm and palm of their left hand. Following each manual estimation trial, participants grasped the target object to equate tasks (i.e., grasping vs. manual estimation) for terminal tactile feedback. Notably, the different object locations (i.e., forearm and palm) were used to examine whether location-specific differences in mechanoreceptor density impacts the percept of object size (i.e., Weber's illusion). In addition, we computed just-noticeable-difference (JND) scores to determine whether grasping and manual estimations adhere to, or violate, the allocentric principles of Weber's law. Results for the grasping task elicited a null expression of Weber's illusion and JNDs for this task violated Weber's law. Results for the manual estimation task similarly exhibited a null expression of Weber's illusion; however, JNDs for the palm but not the forearm condition adhered to Weber's law. Experiment 2 showed that withdrawing terminal tactile feedback during forearm condition manual estimations resulted in responses that adhered to Weber's law. Thus, results provide some support for the SPM's contention that grasping and manual estimations are mediated via ego- and allocentric frames of reference, respectively. However, results further indicate that the dissociation is not complete and is, in part, influenced by the sensory consequences (i.e., terminal tactile feedback) associated with the response.

An antisaccade is the execution of a saccade to the mirror-symmetrical location (i.e., same amplitude but opposite visual field) of a single and exogenously presented visual target. Such a response requires top-down decoupling of the normally direct spatial relations between stimulus and response and results in increased planning times and directional errors compared to their spatially compatible prosaccade counterparts. Moreover, antisaccades are associated with diffuse changes in cortical and subcortical saccade networks: a finding that has, in part, been attributed to pre-setting the oculomotor system to withhold a stimulus-driven prosaccade. Moreover, recent work has shown that a corollary cost of oculomotor pre-setting is that the planning time for a to-be-completed prosaccade is longer when preceded by an antisaccade (i.e., the unidirectional prosaccade switch-cost). Notably, this result has been attributed to antisaccades imparting a residual inhibition of the oculomotor networks that support the planning of stimulus-driven prosaccades. In the current investigation, we sought to determine if the number of antisaccades preceding a prosaccade increases this residual inhibition and thus influences the magnitude of the unidirectional prosaccade switch-cost. To that end, participants alternated between pro- and antisaccades after every second (i.e., AABB schedule) and every fourth (i.e., AAAABBBB schedule) trial. In addition, participants completed pro- and antisaccades in separate blocks of trials. Results demonstrated that task-switch prosaccades produced longer reaction times than their task-repetition and blocked condition counterparts, whereas antisaccade reaction times did not vary across task-repetition, task-switch and blocked condition trials. Most notably, the magnitude of the unidirectional prosaccade switch-cost was not modulated across the different task-switching schedules. Thus, we propose that the top-down requirements of the antisaccade task do not produce additive inhibition of stimulus-driven saccade networks.

An issue of continued debate in the visuomotor control literature surrounds whether a 2D object serves as a representative proxy for a 3D object in understanding the nature of the visual information supporting grasping control. In an effort to reconcile this issue, we examined the extent to which aperture profiles for grasping 2D and 3D objects adheres to, or violates, the psychophysical properties of Weber’s law. Specifically, participants grasped differently sized 2D and 3D objects (20, 30, 40, and 50 mm of width) and we computed the just-noticeable-difference scores associated with aperture profiles at decile increments of normalized grasping time. The aperture profiles for 2D objects showed an early through late (i.e., 10% through 90%) adherence to Weber’s law, whereas the late stages of grasping 3D objects (i.e., >50% of grasping time) produced a fundamental violation of the law’s principles. As such, results suggest that grasping a 2D object is a top-down and cognitive task mediated via relative visual information. In contrast, the enriched shape information provided by a 3D object (i.e., stereoscopic vergence and disparity cues) allows for later aperture specification via absolute (Euclidean) visual information. Most notably, our results establish that the dimensional properties of an object influence the visual information mediating motor output, and further indicate that 2D and 3D objects are not representative proxies for one another in understanding the visual control of grasping.

The antisaccade task requires the suppression of a reflexive prosaccade (i.e., response suppression) and the remapping of a target location to mirror-symmetrical space (i.e., vector inversion). Moreover, antisaccades are associated with increased activation of cortical oculomotor networks: a finding attributed to the top-down requirements of response suppression and vector inversion. The goal of the present study was to determine if the increased cortical activity associated with antisaccades elicits a residual inhibition of oculomotor planning networks. To that end, each trial in this investigation entailed the onset of a single and exogenously presented target (i.e., archetypical antisaccade task) and participants were instructed to alternate between pro- and antisaccades in blocked and random task-switching schedules. In the blocked schedule, the saccade tasks (i.e., pro- and antisaccades) alternated on every second trial (AABB paradigm) whereas in the random schedule the saccade tasks were pseudo-randomly interleaved on a trial-by-trial basis. Reaction times for task-switch prosaccades were longer and more variable than their task-repetition counterparts, whereas antisaccades did not vary as a function of task-switch and task-repetition trials: a finding that was consistent across blocked and random presentation schedules. In other words, results demonstrate a unidirectional switch-cost for prosaccades. As such, we propose that the top-down processes required to complete an antisaccade results in residual inhibition of oculomotor networks supporting a subsequent prosaccade.

The ‘just noticeable difference’ (JND) represents the minimum amount by which a stimulus must change to produce a noticeable variation in one’s perceptual experience and is related to initial stimulus magnitude (i.e., Weber’s law). The goal of the present study was to determine whether aperture shaping for visually derived and memory-guided grasping elicit a temporally dependent or temporally independent adherence to Weber’s law. Participants were instructed to grasp differently sized objects (20, 30, 40, 50 and 60mm) in conditions wherein vision of the grasping environment was available throughout the response (i.e., closed-loop), when occluded at movement onset (i.e., open-loop), and when occluded for a brief (i.e., 0ms) or longer (i.e., 2000ms) delay in advance of movement onset. Within-participant standard deviations of grip aperture (i.e., the JNDs) computed at decile increments of normalized grasping time were used to determine participant’s sensitivity to detecting changes in object size. Results showed that JNDs increased linearly with increasing object size from 10% to 40% of grasping time; that is, the trial-to-trial stability (i.e., visuomotor certainty) of grip aperture (i.e., the comparator) decreased with increasing object size (i.e., the initial stimulus). However, a null JND/object size scaling was observed during the middle and late stages of the response (i.e., >50% of grasping time). Most notably, the temporal relationship between JNDs and object size scaling was similar across the different visual conditions used here. Thus, our results provide evidence that aperture shaping elicits a time-dependent early, but not late, adherence to the psychophysical principles of Weber’s law.

In the visuomotor mental rotation (VMR) task, participants point to a location that deviates from a visual target by a predetermined angle. A seminal investigation of the VMR task reported a linear increase in reaction time (RT) as a function of increasing angle, for 5°, 10°, 15°, 35°, 70°, 105°, and 140° (Georgopoulos and Massey, 1987). This finding led to the development of the mental rotation model (MRM) and the assertion that response preparation is mediated via the imagined rotation of a movement vector. To determine if the MRM can be extrapolated to perceptually familiar angles (e.g., 90° and 180°) within a range of equally spaced angles, we evaluated two independent sets of angles: 5°, 10°, 15°, 35°, 70°, 105°, and 140° (experiment one) and 30°, 60°, 90°, 120°, 150°, 180°, and 210° (experiment two). Consistent with the MRM, experiment one revealed a linear increase in RT as a function of increasing angle; however, a non-linear relation was revealed for experiment two. RTs were fastest for 180°, followed by 30°, 90°, 60°, 150°, 210°, and 120°. Such results demonstrate that response preparation was not uniquely mediated via a mental rotation process. Instead, the present work provides evidence of a temporally demanding and cognitively mediated response substitution process, wherein the computational demands of response preparation are determined by the complexity of the sensorimotor transformations mediating the response.

The goal of the present investigation was to determine whether the anti-pointing task (i.e., pointing to a location 180 degrees from a visual cue [M. Heath, A. Maraj, A. Gradkowski, G. Binsted, Anti-pointing is mediated by a perceptual bias of target location in left and right visual space, Exp. Brain Res. 192 (2009) 275-286]) and a 90 degrees -rotated-pointing task are supported by a similar cognitive strategy. Previous work evaluating visuomotor mental rotation (MR) has reported a monotonic increase in reaction time (RT) as a function of the angle of rotation [A.P. Georgopoulos, G. Pellizzer, The mental and the neural: psychological and neural studies mental rotation and memory scanning, Neuropsychologia 33 (1995) 1531-1547]. Interestingly, however, anti-pointing movements have not been evaluated in concert with intermediary angles of rotation. We therefore examined RT for center-out pointing movements in four tasks: pro-pointing (PRO), anti-pointing (ANTI), and 90 degrees clockwise (CW90) and counter-clockwise (CCW90) pointing. We found that response latencies for PRO responses were faster than ANTI responses, which in turn were faster than CW90 and CCW90 responses. These findings counter the notion that the angle of rotation influences the speed of visuomotor MR. Instead, we posit that visuomotor MR is supported by a serial process requiring the suppression of a stimulus-driven response followed by voluntary response generation. Further, we suggest that preparation of the voluntary response is cognitively less demanding for the ANTI task because the sensorimotor transformations underlying such an action are completed within the same plane as the stimulus-driven response. In contrast, the cognitive demands associated with CW90 and CCW90 are more complex because the action requires the transformation of response parameters in a movement plane orthogonal to the original - and suppressed - stimulus-driven response.

The production of transitive limb gestures is optimized when the appropriate tool can be physically manipulated. Little research has addressed the independent contributions of visual and nonvisual sources of sensory information to this phenomenon. In this study, 12 control, 37 LHD, and 50 RHD stroke patients performed transitive limb gestures to pantomime (to verbal command with the object visible) and object manipulation. Performance was more accurate in the object manipulation condition, suggesting that haptic and kinesthetic cues are important for transitive gesture production. Various patterns of performance were observed in the stroke groups, indicating that selective damage to the haptic/kinesthetic processing system is possible and common following unilateral stroke.

The model of apraxia proposed by Roy (1996) states that three patterns of apraxia should be observed across pantomime and imitation conditions. In the present analysis the frequency and severity of each pattern of apraxia were examined in a consecutive sample of left-(LHD) and right-hemisphere-damaged (RHD) patients during the production of intransitive limb gestures. The results indicated that a significant proportion of LHD and RHD patients were selectively impaired in formulating the ideational component of intransitive limb gestures.

The present study was designed to examine the frequency and severity of apraxia in patients with left- or right-hemisphere stroke in both pantomime and imitation conditions and to compare the frequency of apraxia in each stroke group across the three patterns of apraxia described in Roy's model (Roy, 1996). Ninety-nine stroke patients and 15 age-matched healthy adults performed eight transitive gestures to pantomime and to imitation. Gestural performance was quantified as accuracy on five performance dimensions; a composite score, an arithmetic combination of the five performance dimensions, was used as an index of the overall accuracy. Analyses revealed a comparable proportion of patients in each stroke group were classified as apraxic in the imitation condition, but a higher proportion of left stroke patients were apraxic in the pantomime condition. The severity of apraxia in each stroke group and the performance dimensions affected were, however, comparable. Analyses of the patterns of apraxia (pantomime alone, imitation alone or apraxia in both conditions) revealed a higher frequency of apraxia in both stroke groups for the pattern reflecting apraxia in both conditions, indicating that a disruption at the movement execution stage of gesture performance was most common.

The study of cerebral specialization in persons with Down syndrome (DS) has revealed an anomalous pattern of organization. Specifically, dichotic listening studies (e.g., Elliott & Weeks, 1993) have suggested a left ear/right hemisphere dominance for speech perception for persons with DS. In the current investigation, the cerebral dominance for speech production was examined using the mouth asymmetry technique. In right-handed, nonhandicapped subjects, mouth asymmetry methodology has shown that during speech, the right side of the mouth opens sooner and to a larger degree then the left side (Graves, Goodglass, & Landis, 1982). The phenomenon of right mouth asymmetry (RMA) is believed to reflect the direct access that the musculature on the right side of the face has to the left hemisphere's speech production systems. This direct access may facilitate the transfer of innervatory patterns to the muscles on the right side of the face. In the present study, the lateralization for speech production was investigated in 10 right-handed participants with DS and 10 nonhandicapped subjects. A RMA at the initiation and end of speech production occurred for subjects in both groups. Surprisingly, the degree of asymmetry between groups did not differ, suggesting that the lateralization of speech production is similar for persons with and persons without DS. These results support the biological dissociation model (Elliott, Weeks, & Elliott, 1987), which holds that persons with DS display a unique dissociation between speech perception (right hemisphere) and speech production (left hemisphere).

A number of recent models of limb control have attempted to explain speed-accuracy trade-off in goal-directed movements on the basis of the characteristics of the muscular impulses that are specified prior to movement initiation. In contrast, studies from our laboratory have demonstrated that, even for very rapid aiming movements, the characteristics of the movement trajectory change with the availability of visual information about the position of the limb and the target during the movement. Moreover, when the movement of the limb is perturbed at movement initiation by an electromagnetic force, performers can rapidly adjust their aiming movements in order to hit the target if visual feedback is available. The performer can also rapidly adjust to unexpected changes in target size and amplitude. Visually based adjustments to the movement trajectory can be either discrete or continuous. PsycINFO classification: 2330; 2343