Temporal uncertainty does not affect response latencies of movements produced during startle reactions

Previous research has shown that a startle ‘go’ stimulus, presented at a constant latency with respect to a warning stimulus, is capable of eliciting an intended voluntary movement in a simple reaction time (RT) task at very short latencies without involvement of the cerebral cortex (Carlsen et al. in Exp Brain Res 152:510–518, 2003; J Motor Behav 36:253–264, 2004a; Exp Brain Res 159:301–309 2004b; Valls-Solé et al. in J Physiol 516:931–938, 1999). The purpose of the present experiment was to determine the effect of temporal uncertainty on response latency during an RT task that comprised a startle stimulus. Participants were required to perform an active 20° wrist extension movement in response to an auditory tone that was presented 2,500 to 5,500 ms after a warning stimulus, in 1,000 ms increments. On certain trials the control auditory stimulus (80 dB) was unexpectedly replaced by the startle stimulus (124 dB). When participants were startled the intended voluntary movement was initiated at approximately 70 ms, regardless of foreperiod duration. The magnitude and invariance of response latencies to the startle stimulus suggest that the intended movement had indeed been prepared prior to the arrival of the imperative go stimulus, within 2.5 s of the warning stimulus. Furthermore, there was no evidence that the prepared movement decayed over a period of at least 3 s.     

Online corrections can produce illusory bias during closed-loop pointing

This experiment examined whether the impact of pictorial illusions during the execution of goal-directed reaching movements is attributable to ocular motor signaling. We analyzed eye and hand movements directed toward both the vertex of the Müller–Lyer (ML) figure in a closed-loop procedure. Participants pointed to the right vertex of a visual stimulus in two conditions: a control condition wherein the figure (in-ML, neutral, out-ML) presented at response planning remained unchanged throughout the movement, and an experimental condition wherein a neutral figure presented at response planning was perturbed to an illusory figure (in-ML, out-ML) at movement onset. Consistent with previous work from our group (Heath et al. in Exp Brain Res 158:378–384, 2004; Heath et al. in J Mot Behav 37:179–185, 2005b), action-bias present in both conditions; thus illusory bias was introduced into during online control. Although primary saccades were influenced by illusory configurations (control conditions; see Binsted and Elliott in Hum Mov Sci 18:103–117, 1999a), illusory bias developed within the secondary “corrective” saccades during experimental trials (i.e., following a veridical primary saccade). These results support the position that a unitary spatial representation underlies both action and perception and this representation is common to both the manual and oculomotor systems.     

Action strategies used by children to avoid two vertical obstacles in non-confined space

Information used to determine the action strategies necessary to successfully pass through apertures is based on the dimensions of the individual and the mover’s action capabilities (Warren in J Exp Psychol 10:683–703, 1984; Warren and Whang in J Exp Psychol 13:371–383, 1987). Previous research has demonstrated that when children must pass through small spaces, they will produce a shoulder rotation at apertures 1.6 times their shoulder width and smaller (i.e., critical point) and their avoidance strategies are based more on dynamic than geometric measures (Snapp-Childs and Bingham in Exp Brain Res 198:527–533, 2009; Wilmut and Barnett in Exp Brain Res 210:185–194, 2011). The question remains as to whether similar strategies exist when children are given a choice in their obstacle avoidance strategy. The current study aimed to determine the action strategies employed by children when confronted with a non-confined obstacle avoidance task. Specifically, the study intended to identify the aperture width that elicited a change in action (e.g., a shoulder rotation or a change in travel path). Children (N = 12, mean age = 7.1 years, ±0.2) were instructed to walk along a 10-m path toward a visible goal located at the end of the pathway and avoid colliding with the two vertical obstacles placed halfway (5 m) down the path on either side of the midline. The space between the obstacles ranged between 0.6 and 1.8 times the participant’s shoulder width (presented in increments of 0.2). Results revealed that when the aperture was too small for straight passage, children choose to circumvent the obstacles rather than rotate their shoulders the majority of the time. However, unlike young and older adults (Hackney and Cinelli in Gait Posture 37:93–97, 2013a, Exp Brain Res 225:419–429, 2013b), this strategy was not used consistently. Instead, changes in travel path were highly variable both across participants and within trials. This variability suggests that a true critical point cannot be established for children in this non-confined task. Variable actions at the time of crossing were significantly correlated with the medial–lateral center of mass variability during the approach to the obstacles. These results further support the idea that children’s actions may be more affected by dynamic factors than geometric measures.     

Inhibition of return in cue–target and target–target tasks

Inhibition of return (IOR), the term given for the slowing of a response to a target that appeared at the same location as a previously presented stimulus, has been studied with both target–target (TT; participants respond to each successive event) and cue–target (CT; participants only respond to the second of two events) tasks. Although both tasks have been used to examine the processes and characteristics of IOR, few studies have been conducted to understand if there are any differences in the processes that underlie the IOR that results from ignoring (CT paradigm) or responding to (TT paradigm) the first stimulus. The purpose of the present study was to examine the notion that IOR found in TT tasks represents “true” IOR whereas IOR found in CT tasks consist of both “true” IOR and response inhibition (Coward et al. in Exp Brain Res 155:124–128, 2004). Consistent with the pattern of effects found by Coward et al. (Exp Brain Res 155:124–128, 2004), IOR was larger in the CT task than in the TT task when a single detection response was required (Experiment 1). However, when participants completed one of two spatially-directed responses (rapid aiming movement to the location of the target stimulus), IOR effects from the CT and TT tasks were equal in magnitude (Experiment 2). Rather than CT tasks having an additional response inhibition component, these results suggest that TT tasks may show less of an inhibitory effect because of a facilitatory response repetition effect.     

The stability of rhythmic movement coordination depends on relative speed: the Bingham model supported

Following many studies showing that the coupling in bimanual coordination can be perceptual, Bingham (Ecol Psychol in 16:45–53, 2001; 2004a, b) proposed a dynamical model of such movements. The model contains three key hypotheses: (1) Being able to produce stable coordinative movements is a function of the ability to perceive relative phase, (2) the information to perceive relative phase is relative direction of motion, and (3) the ability to resolve this information is conditioned by relative speed. The first two hypotheses have been well supported (Wilson and Bingham in Percept Psychophys 70:465–476, 2008; Wilson et al. in J Exp Psychol Hum 36:1508–1514, 2010a), but the third was not supported when tested by de Rugy et al. (Exp Brain Res 184:269–273, 2008) using a visual coordination task that required simultaneous control of both the amplitude and relative phase of movement. The purposes of the current study were to replicate this task with additional measures and to modify the original model to apply it to the new task. To do this, we conducted two experiments. First, we tested the ability to produce 180° visual coordination at different frequencies to determine frequencies suitable for testing in the de Rugy et al. task. Second, we tested the de Rugy et al. task but included additional measures that yielded results different from those reported by de Rugy et al. These results were used to elaborate the original model. First, one of the phase-driven oscillators was replaced with a harmonic oscillator, so the resulting coupling was unidirectional. This change resulted in the model producing less stable 180° coordination behavior beyond 1.5 Hz consistent with the results obtained in Experiment 1. Next, amplitude control and phase correction elements were added to the model. With these changes, the model reproduced behaviors observed in Experiment 2. The central finding was that the stability of rhythmic movement coordination does depend on relative speed and, thus, all three of the hypotheses contained in the original Bingham model are supported.     

Aging does not affect generalized postural motor learning in response to variable amplitude oscillations of the support surface

Postural motor learning for dynamic balance tasks has been demonstrated in healthy older adults (Van Ooteghem et al. in Exp Brain Res 199(2):185–193, 2009). The purpose of this study was to investigate the type of knowledge (general or specific) obtained with balance training in this age group and to examine whether embedding perturbation regularities within a balance task masks specific learning. Two groups of older adults maintained balance on a translating platform that oscillated with variable amplitude and constant frequency. One group was trained using an embedded-sequence (ES) protocol which contained the same 15-s sequence of variable amplitude oscillations in the middle of each trial. A second group was trained using a looped-sequence (LS) protocol which contained a 15-s sequence repeated three times to form each trial. All trials were 45 s. Participants were not informed of any repetition. To examine learning, participants performed a retention test following a 24-h delay. LS participants also completed a transfer task. Specificity of learning was examined by comparing performance for repeated versus random sequences (ES) and training versus transfer sequences (LS). Performance was measured by deriving spatial and temporal measures of whole body center of mass (COM) and trunk orientation. Both groups improved performance with practice as characterized by reduced COM displacement, improved COM–platform phase relationships, and decreased angular trunk motion. Furthermore, improvements reflected general rather than specific postural motor learning regardless of training protocol (ES or LS). This finding is similar to young adults (Van Ooteghem et al. in Exp Brain Res 187(4):603–611, 2008) and indicates that age does not influence the type of learning which occurs for balance control.     

An anti-Hick’s effect for exogenous, but not endogenous, saccadic eye movements

Previously, we have shown that the reaction times (RTs) of exogenously generated saccadic eye movements decrease with an increase in the number of response alternatives (Lawrence et al. in J Vis 8(26):1–7, 2008; Lawrence and Gardella in Exp Brain Res 195(3):413–418, 2009). Because this pattern of RTs is in the direction opposite that predicted by Hick (Q J Exp Psychol 4:11–26, 1952), we termed the effect an “anti-Hick’s” effect. In the present study, we examined whether this effect characterizes saccades in general, or only those saccades that are exogenously generated. An anti-Hick’s effect was found for exogenous, but not for endogenous, saccades. These results demonstrate a clear dissociation between exogenously and endogenously generated saccades and place an important constraint on the anti-Hick’s effect.     

Location but not amount of stimulus occlusion influences the stability of visuo-motor coordination

The current study examined whether the amount and location of available movement information influenced the stability of visuo-motor coordination. Participants coordinated a hand-held pendulum with an oscillating visual stimulus in an inphase and antiphase manner. The effects of occluding different amounts of phase at different phase locations were examined. Occluding the 0°/180° phase locations (end-points) significantly increased the variability of the visuo-motor coordination. The amount of occlusion had little or no affect on the stability of the coordination. We concluded that the end-points of a visual rhythm are privileged and provide access to movement information that ensures stable coordination. The results are discussed with respect to the proposal of Bingham and colleagues (e.g., Bingham GP. Ecol Psychol 16:45–53, 2004a; Wilson AD, Collins DR, Bingham GP. Exp Brain Res 165:351–361, 2005a) that the relevant information for rhythmic visual coordination is relative direction information.     

Endogenous orienting is reduced during the attentional blink

We studied endogenous cuing during the attentional blink in order to examine its resistance to dual task interference. In two experiments, we found a reduced impact of endogenous cuing during the “blink” time of the attentional blink. In a third experiment endogenous cuing was intact when it was not influenced by demands imposed by an earlier target. Contrary to a recent report (Zhang et al. in Exp Brain Res, 185, 287–295, 2008), the results indicate that endogenous orienting guided by semantic cues is susceptible to the attentional blink.     

Temporal recalibration during asynchronous audiovisual speech perception

When a participant moves a hand-held target in complete darkness after an afterimage of that target has been obtained, an illusory increase (with movements away from the participant) or decrease (with movements towards the participant) in the apparent size of the afterimage is reported (the Taylor illusion, reported first in Taylor, J Exp Psychol 29: 1941). Unlike typical Emmert’s Law demonstrations, the Taylor illusion shows that a motor-related signal can be used to specify distance for the computation of real size. A study by Carey and Allan (Exp Brain Res 110: 1996) found that the Taylor illusion did not occur in a condition where an afterimage of one hand was obtained while the other hand performed a movement away from the participant from directly behind the first. It was proposed that, for the illusion to manifest itself, proprioceptive and visual information must be in strict “register” when the afterimage is obtained. To evaluate this hypothesis, 14 participants performed “towards” and “away” movements after obtaining afterimages of hand-held cards. Participants wore either plain lenses or prism lenses during the trials, the latter of which displaced visual stimuli 10° to the left. No significant difference was found between the two lens conditions in terms of the effect on the perception of the Taylor illusion. It was concluded that the illusory size distortions may depend on register of visual and proprioceptive position in terms of depth, rather than in the picture plane. Several suggestions for future studies of the Taylor illusion are proposed, and limitations of size judgements of afterimages are outlined.     

Bimanual Fitts’ tasks: Kelso,Southard, and Goodman, 1979 revisited

The experiment was designed to replicate and extend to an integrated feedback condition the pattern of movement time results found by Kelso et al. (J Exp Psychol Hum Percept Perform 5:229–238, 1979a, Science 204:1029–1031, 1979b) where the simultaneous movement of one hand to a low ID target and the other to a higher ID target indicated “a tight coordinate coupling between the hands” (p. 229). In the present experiment, a control group was provided feedback that depicted the independent movement of the two limbs under low and higher indexes of difficulty (ID). A Lissajous group was provided integrated feedback in the form of a Lissajous plot. The results indicated a pattern of results for the control and Lissajous groups similar to that found by Kelso et al. for one and two-limb movements to the same difficulty targets. The control group also replicated the finding for two-limb movements to mixed ID tasks. However, the Lissajous group simultaneously produced disparate movement in the mixed target conditions. The results are consistent with recent findings indicating that when provided salient integrated feedback participants can effectively produce disparate movements of the two limbs.     

Movement chunking during sequence learning is a dopamine-dependant process: a study conducted in Parkinson’s disease

Chunking of single movements into integrated sequences has been described during motor learning, and we have recently demonstrated that this process involves a dopamine-dependant mechanism in animal (Levesque et al. in Exp Brain Res 182:499–508, 2007; Tremblay et al. in Behav Brain Res 198:231–239, 2009). However, there is no such evidence in human. The aim of the present study was to assess this question in Parkinson’s disease (PD), a neurological condition known for its dopamine depletion in the striatum. Eleven PD patients were tested under their usual levodopa medication (ON state), and following a 12-h levodopa withdrawal (OFF state). Patients were compared with 12 healthy participants on a motor learning sequencing task, requiring pressing fourteen buttons in the correct order, which was determined by visual stimuli presented on a computer screen. Learning was assessed from three blocks of 20 trials administered successively. Chunks of movements were intrinsically created by each participant during this learning period. Then, the sequence was shuffled according to the participant’s own chunks, generating two new sequences, with either preserved or broken chunks. Those new motor sequences had to be performed separately in a fourth and fifth blocks of 20 trials. Results showed that execution time improved in every group during the learning period (from blocks 1 to 3). However, while motor chunking occurred in healthy controls and ON-PD patients, it did not in OFF-PD patients. In the shuffling conditions, a significant difference was seen between the preserved and the broken chunks conditions for both healthy participants and ON-PD patients, but not for OFF-PD patients. These results suggest that movement chunking during motor sequence learning is a dopamine-dependent process in human.     

Differential working memory correlates for implicit sequence performance in young and older adults

Our recent work has revealed that visuospatial working memory (VSWM) relates to the rate of explicit motor sequence learning (Bo and Seidler in J Neurophysiol 101:3116–3125, 2009) and implicit sequence performance (Bo et al. in Exp Brain Res 214:73–81, 2011a) in young adults (YA). Although aging has a detrimental impact on many cognitive functions, including working memory, older adults (OA) still rely on their declining working memory resources in an effort to optimize explicit motor sequence learning. Here, we evaluated whether age-related differences in VSWM and/or verbal working memory (VWM) performance relates to implicit performance change in the serial reaction time (SRT) sequence task in OA. Participants performed two computerized working memory tasks adapted from change detection working memory assessments (Luck and Vogel in Nature 390:279–281, 1997), an implicit SRT task and several neuropsychological tests. We found that, although OA exhibited an overall reduction in both VSWM and VWM, both OA and YA showed similar performance in the implicit SRT task. Interestingly, while VSWM and VWM were significantly correlated with each other in YA, there was no correlation between these two working memory scores in OA. In YA, the rate of SRT performance change (exponential fit to the performance curve) was significantly correlated with both VSWM and VWM, while in contrast, OA’s performance was only correlated with VWM, and not VSWM. These results demonstrate differential reliance on VSWM and VWM for SRT performance between YA and OA. OA may utilize VWM to maintain optimized performance of second-order conditional sequences.     

Left,right, left,right, eyes to the front! Müller-Lyer bias in grasping is not a function of hand used,hand preferred or visual hemifield,but foveation does matter

We investigated whether the control of movement of the left hand is more likely to involve the use of allocentric information than movements performed with the right hand. Previous studies (Gonzalez et al. in J Neurophys 95:3496–3501, 2006; De Grave et al. in Exp Br Res 193:421–427, 2009) have reported contradictory findings in this respect. In the present study, right-handed participants (N = 12) and left-handed participants (N = 12) made right- and left-handed grasps to foveated objects and peripheral, non-foveated objects that were located in the right or left visual hemifield and embedded within a Müller-Lyer illusion. They were also asked to judge the size of the object by matching their hand aperture to its length. Hand apertures did not show significant differences in illusory bias as a function of hand used, handedness or visual hemifield. However, the illusory effect was significantly larger for perception than for action, and for the non-foveated compared to foveated objects. No significant illusory biases were found for reach movement times. These findings are consistent with the two-visual system model that holds that the use of allocentric information is more prominent in perception than in movement control. We propose that the increased involvement of allocentric information in movements toward peripheral, non-foveated objects may be a consequence of more awkward, less automatized grasps of nonfoveated than foveated objects. The current study does not support the conjecture that the control of left-handed and right-handed grasps is predicated on different sources of information.     

Supra-spinal circuits shape inhibitory postural adjustments anticipating voluntary index-finger flexion

We investigated the influence of gaze elevation on judging the possibility of passing under high obstacles during pitch body tilts, while stationary, in absence of allocentric cues. Specifically, we aimed at studying the influence of egocentric references upon geocentric judgements. Seated subjects, orientated at various body orientations, were asked to perceptually estimate the possibility of passing under a projected horizontal line while keeping their gaze on a fixation target and imagining a horizontal body displacement. The results showed a global overestimation of the possibility of passing under the line, and confirmed the influence of body orientation reported by Bringoux et al. (Exp Brain Res 185(4):673–680, 2008). More strikingly, a linear influence of gaze elevation was found on perceptual estimates. Precisely, downward eye elevation yielded increased overestimations, and conversely upward gaze elevation yielded decreased overestimations. Furthermore, body and gaze orientation effects were independent and combined additively to yield a global egocentric influence with a weight of 45 and 54%, respectively. Overall, our data suggest that multiple egocentric references can jointly affect the estimated possibility of passing under high obstacles. These results are discussed in terms of “interpenetrability” between geocentric and egocentric reference frames and clearly demonstrate that gaze elevation is involved, as body orientation, in geocentric spatial localization.     

Overlapping functional anatomy for working memory and visual search

Recent behavioural findings using dual-task paradigms demonstrate the importance of both spatial and non-spatial working memory processes in inefficient visual search (Anderson et al. in Exp Psychol 55:301–312, 2008). Here, using functional magnetic resonance imaging (fMRI), we sought to determine whether brain areas recruited during visual search are also involved in working memory. Using visually matched spatial and non-spatial working memory tasks, we confirmed previous behavioural findings that show significant dual-task interference effects occur when inefficient visual search is performed concurrently with either working memory task. Furthermore, we find considerable overlap in the cortical network activated by inefficient search and both working memory tasks. Our findings suggest that the interference effects observed behaviourally may have arisen from competition for cortical processes subserved by these overlapping regions. Drawing on previous findings (Anderson et al. in Exp Brain Res 180:289–302, 2007), we propose that the most likely anatomical locus for these interference effects is the inferior and middle frontal cortex of the right hemisphere. These areas are associated with attentional selection from memory as well as manipulation of information in memory, and we propose that the visual search and working memory tasks used here compete for common processing resources underlying these mechanisms.     

Audio-visual facilitation of the mu rhythm

Previous studies demonstrate that perception of action presented audio-visually facilitates greater mirror neuron system (MNS) activity in humans (Kaplan and Iacoboni in Cogn Process 8(2):103–113, 2007) and non-human primates (Keysers et al. in Exp Brain Res 153(4):628–636, 2003) than perception of action presented unimodally. In the current study, we examined whether audio-visual facilitation of the MNS can be indexed using electroencephalography (EEG) measurement of the mu rhythm. The mu rhythm is an EEG oscillation with peaks at 10 and 20 Hz that is suppressed during the execution and perception of action and is speculated to reflect activity in the premotor and inferior parietal cortices as a result of MNS activation (Pineda in Behav Brain Funct 4(1):47, 2008). Participants observed experimental stimuli unimodally (visual-alone or audio-alone) or bimodally during randomized presentations of two hands ripping a sheet of paper, and a control video depicting a box moving up and down. Audio-visual perception of action stimuli led to greater event-related desynchrony (ERD) of the 8–13 Hz mu rhythm compared to unimodal perception of the same stimuli over the C3 electrode, as well as in a left central cluster when data were examined in source space. These results are consistent with Kaplan and Iacoboni’s (in Cogn Process 8(2):103–113, 2007), findings that indicate audio-visual facilitation of the MNS; our left central cluster was localized approximately 13.89 mm away from the ventral premotor cluster identified in their fMRI study, suggesting that these clusters originate from similar sources. Consistency of results in electrode space and component space support the use of ICA as a valid source localization tool.     

Grasp effects of the Ebbinghaus illusion are ambiguous

The assumption that the Ebbinghaus/Titchener illusion deceives perception but not grasping, which would confirm the two-visual-systems hypothesis (TVSH) as proposed by Milner and Goodale (The visual brain in action, 1995), has recently been challenged. Franz et al. (Exp Brain Res 149:470–477, 2003) found that the illusion affects both perception and grasping, and showed that the effect of the illusion on the peak grip aperture (PGA) cannot be accounted for by different sizes of the gap that separates the central target disk from the surrounding flankers. However, it is not yet clear if the presence of flankers per se influences grasping. We therefore compared kinematic parameters of prehension, using the Ebbinghaus illusion, and a neutral control condition where normal subjects grasped a disk without any flankers. In accordance with the well-known effects of the illusion on perceived size, the PGA was smaller when the target disk was surrounded by large flankers, and larger when it was encircled by small flankers. However, the largest PGA values were reached in the neutral control condition. Hence the presence of flankers leads to a general reduction of the PGA, possibly because the flankers are regarded as obstacles. This ‘reduction effect’ casts doubts on how appropriate it is to directly compare perceptual measures and PGA values when using the Ebbinghaus illusion. Even smaller effects of the illusion on the PGA compared to larger perceptual effects cannot be unequivocally interpreted.     

Visuomotor mental rotation: the reaction time advantage for anti-pointing is not influenced by perceptual experience with the cardinal axes

In the visuomotor mental rotation (VMR) paradigm, participants execute a center-out reaching movement to a location that deviates from a visual cue by a predetermined instruction angle. Previous work has demonstrated a linear increase in reaction time (RT) as a function of the amplitude of the instruction angle (Georgopoulos and Massey in Exp Brain Res 65:361–370, 1987). In contrast, we recently reported a RT advantage for an instruction angle of 180° relative to a 90° angle (Neely and Heath in Neurosci Lett 463:194–198, 2009). It is possible, however, that perceptual expertise with the cardinal axes, which are perceptually familiar reference frames, influenced the results of our previous investigation. To address this issue, we employed a VMR paradigm identical to that of our previous work, with the exception that the stimulus array was shifted 45° from the horizontal and vertical meridians. Our results demonstrated that RTs were fastest and least variable when the instruction angle was 0°, followed by 180°, which in turn, was faster than 90°. Such findings establish that the RT advantage for the 180° instruction angle is not influenced by perceptual expertise with the cardinal axes. Moreover, the present results provide convergent evidence that RT is not determined by the angle of rotation; instead, they indicate that response latencies reflect computational differences in the complexity of response remapping.     

Misperceiving the speed-accuracy tradeoff: imagined movements and perceptual decisions

Research has suggested that prospective motor decisions are consistent with actual motor action. In a study that we recently published (Young et al. in Exp Brain Res 185:681–688, 2008), however, participants demonstrated a preference for closer targets that was inconsistent with the predictions of Fitts’s law. With a pair of experiments, the present paper investigates the underlying basis of this non-optimal behaviour. Participants showed a similar deviation from Fitts’s law when imagining movements—believing that movement duration increased with distance within the same index of difficulty. Participants did not behave similarly, however, in a perceptual version of the decision task. These results suggest that imagined movements and motor decisions are linked, as well as demonstrating one situation in which both show a similar deviation from the patterns of actual movement duration.