Biomedical subjects

Philip Servos

Publications and source records attributed to Philip Servos.

10 recordsLinked to original sources

PubMed2006

The influence of familiarity on brain activation during haptic exploration of 3-D facemasks.

Little is known about the neural substrates that underlie difficult haptic discrimination of 3-D within-class object stimuli. Recent work [A.R. Kilgour, R. Kitada, P. Servos, T.W. James, S.J. Lederman, Haptic face identification activates ventral occipital and temporal areas: an fMRI study, Brain Cogn. (in press)] suggests that the left fusiform gyrus may contribute to the identification of facemasks that are haptically explored in the absence of vision. Here, we extend this line of research to investigate the influence of familiarity. Subjects were trained extensively to individuate a set of facemasks in the absence of vision using only haptic exploration. Brain activation was then measured using fMRI while subjects performed a haptic face recognition task on familiar and unfamiliar facemasks. A group analysis contrasting familiar and unfamiliar facemasks found that the left fusiform gyrus produced greater activation with familiar facemasks.

Adult↗

PubMed2006

Preservation of Emmert's law in a visual form agnosic.

Size constancy was investigated in DF, a patient with visual form agnosia, using a technique based on Emmert's law of visual after-images. DF was first given a task in which she was asked to indicate the distance of a vertical surface and a task where she had to estimate the width of a series of squares (widths ranging from 5 cm to 35 cm) placed at varying distances and having a constant visual angle. In the distance estimation task, DF greatly overestimated the distance of the vertical surface placed in front of her. DF also had great difficulty performing the size estimation task. DF then performed a task in which she stared at a bright 5 cm square for a brief period of time at a distance of 30 cm followed by the presentation of a vertical surface which varied in distance and was asked to indicate the width of the after-image either verbally or manually. DF's after-images conformed to the size-distance relationship predicted by Emmert's law--as the distance of the vertical surface increased her perception of the size of the after-images also increased. These data demonstrate that although DF is rather impaired in tasks that require explicit estimates of size and distance, at some level, DF must have relatively intact size constancy mechanisms given that her estimates of the width of the after-image conform to Emmert's law. Thus, the processes underlying explicit judgements of size and distance appear to differ from those underlying the size and distance scaling of after-images.

Adult↗

PubMed2005

Haptic face identification activates ventral occipital and temporal areas: an fMRI study.

Many studies in visual face recognition have supported a special role for the right fusiform gyrus. Despite the fact that faces can also be recognized haptically, little is known about the neural correlates of haptic face recognition. In the current fMRI study, neurologically intact participants were intensively trained to identify specific facemasks (molded from live faces) and specific control objects. When these stimuli were presented in the scanner, facemasks activated left fusiform and right hippocampal/parahippocampal areas (and other regions) more than control objects, whereas the latter produced no activity greater than the facemasks. We conclude that these ventral occipital and temporal areas may play an important role in the haptic identification of faces at the subordinate level. We further speculate that left fusiform gyrus may be recruited more for facemasks than for control objects because of the increased need for sequential processing by the haptic system.

Adult↗

PubMed2005

Recognizing partially visible objects.

In two experiments we measured object recognition performance as a function of delay. In Experiment 1 we presented half of an image of an object, and then the other half after a variable delay. Objects were subdivided into top versus bottom halves, left versus right halves, or vertical strips. In Experiment 2 we separated the low (LSF) and high spatial frequency (HSF) components of an image, and presented one component followed by the other after a variable delay. For both experiments, performance was worse with a 105ms delay between the presentations of the object components than when the two components were presented simultaneously. These results are consistent with predictions made by models that combine information at a relatively early stage in processing. In addition, the results revealed that object recognition performance is significantly better when the LSF sub-image preceded the HSF sub-image than when the HSF sub-image preceded the LSF sub-image, consistent with previous work suggesting that LSF information is processed prior to HSF in object recognition.

Adult↗

PubMed2004

When two eyes are better than one in prehension: monocular viewing and end-point variance.

Previous research has suggested that binocular vision plays an important role in prehension. It has been shown that removing binocular vision affects (negatively) both the planning and on-line control of prehension. It has been suggested that the adverse impact of removing binocular vision is because monocular viewing results in an underestimation of target distance in visuomotor tasks. This suggestion is based on the observation that the kinematics of prehension are altered when viewing monocularly. We argue that it is not possible to draw unambiguous conclusions regarding the accuracy of distance perception from these data. In experiment 1, we found data that contradict the idea that a consistent visuomotor underestimation of target distance is an inevitable consequence of monocular viewing. Our data did show, however, that positional variance increases under monocular viewing. We provide an alternative explanation for the kinematic changes found when binocular vision is removed. Our account is based on the changes in movement kinematics that occur when end-point variance is altered following the removal of binocular vision. We suggest that the removal of binocular vision leads to greater perceptual uncertainty (e.g. less precise stimulus cues), resulting in changes in the kinematics of the movement (longer duration movements). Our alternative account reconciles some differences within the research literature. We conducted a series of experiments to explore further the issue of when binocular information is advantageous in prehension. Three subsequent experiments were employed which varied binocular/monocular viewing in selectively lit conditions. Experiment 2 explored the differences in prehension measured between monocular and binocular viewing in a full cue environment with a continuous view of the target object. Experiment 3 required participants to reach, under a monocular or binocular view, for a continuously visible self-illuminated target object in an otherwise dark room. In Experiment 3, the participant could neither see the target object nor the reaching hand following initiation of the prehension movement. Our results suggest that binocular vision contributes to prehension by providing additional information (cues) to the nervous system. These cues appear to be weighted differentially according to the particular constellation of stimulus cues available to the participants when reaching to grasp. One constant advantage of a binocular view appears to be the provision of on-line information regarding the position of the hand relative to the target. In reduced cue conditions (i.e. where a view of the target object is lost following initiation of the movement), binocular information regarding target location appears to be particularly useful in the initial programming of reach distance. Our results are a step towards establishing the specific contributions that binocular vision makes to the control of prehension.

Biomechanical Phenomena↗

PubMed2004

Distributed digit somatotopy in primary somatosensory cortex.

We obtained high-resolution somatotopic maps of the human digits using 4.0 T functional magnetic resonance imaging (fMRI). In separate experiments, the volar surface of either the right thumb, index, or ring finger was stimulated in a sliding-window fashion in both distal-to-proximal and proximal-to-distal directions using a custom-built pneumatic apparatus. Analysis of the functional images was restricted to Brodmann's areas 3b and 1 and control areas 4 and 3a, as well as a randomized simulation of the functional data in each of these areas. Using in-house algorithms, we detected discrete regions of cortical activation showing phase reversal coinciding with alternation in stimulation direction. Most stimulation-related phase maps of the digits were obtained in areas 3b and 1, rather than areas 3a or 4, despite the somatic input to the latter two areas. The area 3b and 1 representations thus appear to be relatively discrete and somatotopic compared to other somatic processing regions. Our results within areas 3b and 1 confirm the nonlinear mapping of the body surface suggested by recordings in nonhuman primates in terms of phase band topography, scaling, and frequency relative to the actual digit surfaces. The scaling and frequency nonlinearities were more evident within area 3b than area 1, suggesting a functional differentiation of these regions as has previously been observed only in more invasive recordings. Specifically, the area 1 representations were larger overall than those observed in area 3b, and the frequencies of area 3b phase bands and voxels were related disproportionately to thumb and index finger stimulation and to particular areas on the digit surface, suggesting a weighting based in part on receptor distribution.

Adult↗

PubMed2003

Perceiving biological motion: dissociating visible speech from walking.

Neuropsychological research suggests that the neural system underlying visible speech on the basis of kinematics is distinct from the system underlying visible speech of static images of the face and identifying whole-body actions from kinematics alone. Functional magnetic resonance imaging was used to identify the neural systems underlying point-light visible speech, as well as perception of a walking/jumping point-light body, to determine if they are independent. Although both point-light stimuli produced overlapping activation in the right middle occipital gyrus encompassing area KO and the right inferior temporal gyrus, they also activated distinct areas. Perception of walking biological motion activated a medial occipital area along the lingual gyrus close to the cuneus border, and the ventromedial frontal cortex, neither of which was activated by visible speech biological motion. In contrast, perception of visible speech biological motion activated right V5 and a network of motor-related areas (Broca's area, PM, M1, and supplementary motor area (SMA)), none of which were activated by walking biological motion. Many of the areas activated by seeing visible speech biological motion are similar to those activated while speech-reading from an actual face, with the exception of M1 and medial SMA. The motor-related areas found to be active during point-light visible speech are consistent with recent work characterizing the human "mirror" system (Rizzolatti, Fadiga, Gallese, & Fogassi, 1996).

Adult↗

PubMed2002

Grasping two-dimensional images and three-dimensional objects in visual-form agnosia.

Visually guided prehension is controlled by a specialized visuomotor system in the posterior parietal cortex. It is not clear how this system responds to visual stimuli that lack three-dimensional (3D) structure, such as two-dimensional (2D) images of objects. We asked a neurological patient with visual-form agnosia (patient D.F.) to grasp 3D objects and 2D images of the same objects and to estimate their sizes manually. D.F.'s grip aperture was scaled to the sizes of the 2D and 3D target stimuli, but her manual estimates were poorly correlated with object size. Control participants demonstrated appropriate size-scaling in both the grasping and manual size-estimation tasks, but tended to use a smaller peak aperture when reaching to grasp 2D images. We conclude that: (1) the dorsal stream grasping system does not discriminate in a fundamental way between 2D and 3D objects, and (2) neurologically normal participants might adopt a different visuomotor strategy for target objects that are recognized to be ungraspable. These findings are consistent with the view that the dorsal grasping system accesses a pragmatic, spatial representation of the target object, whereas the ventral system accesses a more comprehensive, volumetric description of the object.

Adult↗

PubMed2002

Haptic study of three-dimensional objects activates extrastriate visual areas.

In humans and many other primates, the visual system plays the major role in object recognition. But objects can also be recognized through haptic exploration, which uses our sense of touch. Nonetheless, it has been argued that the haptic system makes use of 'visual' processing to construct a representation of the object. To investigate possible interactions between the visual and haptic systems, we used functional magnetic resonance imaging to measure the effects of cross-modal haptic-to-visual priming on brain activation. Subjects studied three-dimensional novel clay objects either visually or haptically before entering the scanner. During scanning, subjects viewed visually primed, haptically primed, and non-primed objects. They also haptically explored non-primed objects. Visual and haptic exploration of non-primed objects produced significant activation in several brain regions, and produced overlapping activation in the middle occipital area (MO). Viewing visually and haptically primed objects produced more activation than viewing non-primed objects in both area MO and the lateral occipital area (LO). In summary, haptic exploration of novel three-dimensional objects produced activation, not only in somatosensory cortex, but also in areas of the occipital cortex associated with visual processing. Furthermore, previous haptic experience with these objects enhanced activation in visual areas when these same objects were subsequently viewed. Taken together, these results suggest that the object-representation systems of the ventral visual pathway are exploited for haptic object perception.

Adult↗

PubMed2002

The neural substrates of biological motion perception: an fMRI study.

We used fMRI to identify the brain areas related to the perception of biological motion (4 T EPI; whole brain). In experiment 1, 10 subjects viewed biological motion (a human figure jumping up and down, composed of 21 dots), alternating with a control stimulus created by applying autoregressive models to the biological motion stimulus (such that the dots' speeds and amplitudes were preserved whereas their linking structure was not). The lengths of the stimulus bouts varied, and therefore the transitions between biological motion and control stimuli were unpredictable. Subjects had to indicate with a button press when each transition occurred. In a related biological motion task, subjects detected short (1 s) disturbances within these displays. We also examined the neural substrates of motion and shape perception, as well as motor imagery, to determine whether or not the cortical regions involved in these processes are also recruited during biological motion perception. Subjects viewed linear motion displays alternating with static dots and a series of common objects alternating with band-limited white noise patterns. Subjects also generated imagery of their own arm movements alternating with visual imagery of common objects. Biological motion specific BOLD signal was found within regions of the lingual gyrus at the cuneus border, showing little overlap with object recognition, linear motion or motion imagery areas. The lingual gyrus activation was replicated in a second experiment that also mapped retinotopic visual areas in three subjects. The results suggest that a region of the lingual gyrus within VP is involved in higher-order processing of motion information.

Adult↗