Biomedical subjects

Robert F Dougherty

Publications and source records attributed to Robert F Dougherty.

10 recordsLinked to original sources

PubMed2006

Differential sensitivity to words and shapes in ventral occipito-temporal cortex.

Efficient extraction of shape information is essential for proficient reading but the role of cortical mechanisms of shape analysis in word reading is not well understood. We studied cortical responses to written words while parametrically varying the amount of visual noise applied to the word stimuli. In only a few regions along the ventral surface, cortical responses increased with word visibility. We found consistently increasing responses in bilateral posterior occipito-temporal sulcus (pOTS), at an anatomical location that closely matches the "visual word form area". In other cortical regions, such as V1, responses remained constant regardless of the noise level. We performed 3 additional tests to assess the functional specialization of pOTS responses for written word processing. We asked whether pOTS responses are 1) left lateralized, 2) more sensitive to words than to line drawings or false fonts, and 3) invariant for visual hemifield of words but not other stimuli. We found that left and right pOTS response functions both had highest sensitivity for words, intermediate for line drawings, and lowest for false fonts. Visual hemifield invariance was similar for words and line drawings. These results suggest that left and right pOTS are both involved in shape processing, with enhanced efficiency for processing visual word forms.

Adult↗

PubMed2006

No functional magnetic resonance imaging evidence for brightness and color filling-in in early human visual cortex.

The brightness and color of a surface depends on its contrast with nearby surfaces. For example, a gray surface can appear very light when surrounded by a black surface or dark when surrounded by a white surface. Some theories suggest that perceived surface brightness and color is represented explicitly by neural signals in cortical visual field maps; these neural signals are not initiated by the stimulus itself but rather by the contrast signals at the borders. Here, we use functional magnetic resonance imaging (fMRI) to search for such neural "filling-in" signals. Although we find the usual strong relationship between local contrast and fMRI response, when perceived brightness or color changes are induced by modulating a surrounding field, rather than the surface itself, we find there is no corresponding local modulation in primary visual cortex or other nearby retinotopic maps. Moreover, when we model the obtained fMRI responses, we find strong evidence for contributions of both local and long-range edge responses. We argue that such extended edge responses may be caused by neurons previously identified in neurophysiological studies as being brightness responsive, a characterization that may therefore need to be revised. We conclude that the visual field maps of human V1 and V2 do not contain filled-in, topographical representations of surface brightness and color.

Action Potentials↗

PubMed2005

Functional organization of human occipital-callosal fiber tracts.

Diffusion tensor imaging (DTI) and fiber tracking (FT) were used to measure the occipital lobe fiber tracts connecting the two hemispheres in individual human subjects. These tracts are important for normal vision. Also, damage to portions of these tracts is associated with alexia. To assess the reliability of the DTI-FT measurements, occipital-callosal projections were estimated from each subject's left and right hemispheres independently. The left and right estimates converged onto the same positions within the splenium. We further characterized the properties of the estimated occipital-callosal fiber tracts by combining them with functional MRI. We used functional MRI to identify visual field maps in cortex and labeled fibers by the cortical functional response at the fiber endpoint. This labeling reveals a regular organization of the fibers within the splenium. The dorsal visual maps (dorsal V3, V3A, V3B, V7) send projections through a large band in the middle of the splenium, whereas ventral visual maps (ventral V3, V4) send projections through the inferior-anterior corner of the splenium. The agreement between the independent left/right estimates, further supported by previous descriptions of homologous tracts in macaque, validates the DTI-FT methods. However, a principal limitation of these methods is low sensitivity: a large number of fiber tracts that connect homotopic regions of ventral and lateral visual cortex were undetected. We conclude that most of the estimated tracts are real and can be localized with a precision of 1-2 mm, but many tracts are missed because of data and algorithm limitations.

Adult↗

PubMed2005

Visual field map clusters in human cortex.

We describe the location and general properties of nine human visual field maps. The cortical location of each map, as well as many examples of the eccentricity and angular representations within these maps, are shown in a series of images that summarize a large set of functional MRI data. The organization and properties of these maps are compared and contrasted with descriptions by other investigators. We hypothesize that the human visual field maps are arranged in several clusters, each comprising a group of maps that share a common foveal representation and semicircular eccentricity map. The spatial organization of these clusters suggests that the perceptual processing within each cluster serves related functions.

Brain Mapping↗

PubMed2005

Cross-subject comparison of principal diffusion direction maps.

Diffusion tensor imaging (DTI) data differ fundamentally from most brain imaging data in that values at each voxel are not scalars but 3 x 3 positive definite matrices also called diffusion tensors. Frequently, investigators simplify the data analysis by reducing the tensor to a scalar, such as fractional anisotropy (FA). New statistical methods are needed for analyzing vector and tensor valued imaging data. A statistical model is proposed for the principal eigenvector of the diffusion tensor based on the bipolar Watson distribution. Methods are presented for computing mean direction and dispersion of a sample of directions and for testing whether two samples of directions (e.g., same voxel across two groups of subjects) have the same mean. False discovery rate theory is used to identify voxels for which the two-sample test is significant. These methods are illustrated in a DTI data set collected to study reading ability. It is shown that comparison of directions reveals differences in gross anatomic structure that are invisible to FA.

Algorithms↗

PubMed2005

Children's reading performance is correlated with white matter structure measured by diffusion tensor imaging.

We investigated the white matter structure in children (n = 14) with a wide range of reading performance levels using diffusion tensor imaging (DTI), a form of magnetic resonance imaging. White matter structure in a left temporo-parietal region that had been previously described as covarying with reading skill in adult readers also differs between children who are normal and poor readers. Specifically, the white matter structure measured using fractional anisotropy (FA) and coherence index (CI) significantly correlated with behavioral measurements of reading, spelling, and rapid naming performance. In general, lower anisotropy and lower coherence were associated with lower performance scores. Although the magnitude of the differences in children are smaller than those in adults, the results support the hypothesis that the structure of left temporoparietal neural pathways is a significant component of the neural system needed to develop fluent reading.

Adolescent↗

PubMed2005

Occipital-callosal pathways in children: Validation and atlas development.

Diffusion tensor imaging and fiber tracking were used to measure fiber bundles connecting the two occipital lobes in 53 children of 7-12 years of age. Independent fiber bundle estimates originating from the two hemispheres converge onto the lower half of the splenium. This observation validates the basic methodology and suggests that most occipital-callosal fibers connect the two occipital lobes. Within the splenium, fiber bundles are organized in a regular pattern with respect to their cortical projection zones. Visual cortex dorsal to calcarine projects through a large band that fills much of the inferior half of the splenium, while cortex ventral to calcarine sends projections through a band at the anterior inferior edge of the splenium. Pathways projecting to the occipital pole and lateral-occipital regions overlap the dorsal and ventral groups slightly anterior to the center of the splenium. To visualize these pathways in a typical brain, we combined the data into an atlas. The estimated occipital-callosal fiber paths from the atlas form the walls of the occipital horn of the lateral ventricle, with dorsal paths forming the medial wall and the ventral paths bifurcating into a medial tract to form the inferior-medial wall and a superior tract that joins the lateral-occipital paths to form the superior wall of the ventricle. The properties of these fiber bundles match those of the hypothetical pathways described in the neurological literature on alexia.

Anatomy, Artistic↗

PubMed2004

Psychophysical indexes of temporal processing abnormalities in children with developmental dyslexia.

Children with dyslexia and children progressing normally in reading performed several perceptual tasks to determine (a) the psychophysical measures that best differentiate children with dyslexia from children with average reading abilities; (b) the extent of temporal processing deficits in a single, well-defined group of children with dyslexia; and (c) the co-occurrence of visual and auditory temporal processing deficits in children with dyslexia. 4 of our 12 psychophysical tasks indicated differences in temporal processing ability between children with dyslexia and children with good reading skills. These included 2 auditory tasks (dichotic pitch perception and FM tone discrimination) and 2 visual tasks (global motion perception and contrast sensitivity). The battery of 12 tasks successfully classified 80% of the children into their respective reading-level groups. Within the group of children with dyslexia who had temporal processing deficits, most were affected in either audition or vision; few children were affected in both modalities. The observed deficits suggest that impaired temporal processing in dyslexia is most evident on tasks that require the ability to synthesize local, temporally modulated inputs into a global percept and the ability to extract the resultant global percept from a noisy environment.

Adolescent↗

PubMed2003

Visual field representations and locations of visual areas V1/2/3 in human visual cortex.

The position, surface area and visual field representation of human visual areas V1, V2 and V3 were measured using fMRI in 7 subjects (14 hemispheres). Cortical visual field maps of the central 12 deg were measured using rotating wedge and expanding ring stimuli. The boundaries between areas were identified using an automated procedure to fit an atlas of the expected visual field map to the data. All position and surface area measurements were made along the boundary between white matter and gray matter. The representation of the central 2 deg of visual field in areas V1, V2, V3 and hV4 spans about 2100 mm2 and is centered on the lateral-ventral aspect of the occipital lobes at Talairach coordinates -29, -78, -11 and 25, -80, -9. The mean area between the 2-deg and 12-deg eccentricities for the primary visual areas was: V1: 1470 mm2; V2: 1115 mm2; and V3: 819 mm2. The sizes of areas V1, V2 and V3 varied by about a factor of 2.5 across individuals; the sizes of V1 and V2 are significantly correlated within individuals, but there is a very low correlation between V1 and V3. These in vivo measurements of normal human retinotopic visual areas can be used as a reference for comparison to unusual cases involving developmental plasticity, recovery from injury, identifying homology with animal models, or analyzing the computational resources available within the visual pathways.

Brain Mapping↗

PubMed2002

Retinotopy and functional subdivision of human areas MT and MST.

We performed a series of functional magnetic resonance imaging experiments to divide the human MT+ complex into subregions that may be identified as homologs to a pair of macaque motion-responsive visual areas: the middle temporal area (MT) and the medial superior temporal area (MST). Using stimuli designed to tease apart differences in retinotopic organization and receptive field size, we established a double dissociation between two distinct MT+ subregions in 8 of the 10 hemispheres studied. The first subregion exhibited retinotopic organization but did not respond to peripheral ipsilateral stimulation, indicative of smaller receptive fields. Conversely, the second subregion within MT+ did not demonstrate retinotopic organization but did respond to peripheral stimuli in both the ipsilateral and contralateral visual hemifields, indicative of larger receptive fields. We tentatively identify these subregions as the human homologues of macaque MT and MST, respectively. Putative human MT and MST were typically located on the posterior/ventral and anterior/dorsal banks of a dorsal/posterior limb of the inferior temporal sulcus, similar to their relative positions in the macaque superior temporal sulcus.

Adult↗