Frith and Happe (Frith, U., & Happe, F. (1994). Autism: Beyond theory of mind. Cognition, 50, 115-132) argue that individuals with autism exhibit 'weak central coherence': an inability to integrate elements of information into coherent wholes. Some authors have speculated that a high-level impairment might be present in the dorsal visual pathway in autism, and furthermore, that this might account for weak central coherence, at least at the visuospatial level. We assessed the integrity of the dorsal visual pathway in children diagnosed with an autism spectrum disorder (ASD), and in typically developing children, using two visual tasks, one examining functioning at higher levels of the dorsal cortical stream (Global Dot Motion (GDM)), and the other assessing lower-level dorsal stream functioning (Flicker Contrast Sensitivity (FCS)). Central coherence was tested using the Children's Embedded Figures Test (CEFT). Relative to the typically developing children, the children with ASD had shorter CEFT latencies and higher GDM thresholds but equivalent FCS thresholds. Additionally, CEFT latencies were inversely related to GDM thresholds in the ASD group. These outcomes indicate that the elevated global motion thresholds in autism are the result of high-level impairments in dorsal cortical regions. Weak visuospatial coherence in autism may be in the form of abnormal cooperative mechanisms in extra-striate cortical areas, which might contribute to differential performance when processing stimuli as Gestalts, including both dynamic (i.e., global motion perception) and static (i.e., disembedding performance) stimuli.
Contrast thresholds for sine-wave gratings of spatial frequencies of 2, 4, 12, and 16 cycles per degree were determined for normal and disabled readers at a range of stimulus durations. Normal readers demonstrated monotonically decreasing sensitivity with increasing spatial frequency at exposure durations between 40 and 100 milliseconds. At exposure durations of 150 to 1000 milliseconds, they showed peak sensitivity at 4 cycles per degree. In comparison, disabled readers showed monotonically decreasing sensitivity with increasing spatial frequency at all stimulus durations. The difference in sensitivity pattern across spatial frequencies was greatest at stimulus durations approximately equal to fixation durations during reading.
This study was designed to determine whether cortical motion processing abnormalities are present in individuals with migraine. Performance was measured using a visual motion coherence task (motion coherence perimetry, MCP) thought to depend on the operation of cortical area V5. Motion coherence thresholds were measured using stimuli composed of moving dots at 17 locations in the central +/- 20 degrees of visual field. Pre-cortical visual function was also measured using frequency doubling perimetry (FDP) at the same 17 locations. Several migraine subjects demonstrated significant pre-cortical visual functional abnormalities, however, most subjects had normal visual fields measured with FDP. Abnormal MCP performance was measured in 15 of 19 migraine-with-aura subjects, and 11 of 17 migraine-without-aura subjects. A decreased ability to detect coherent motion may possibly be explained by an increase in baseline neuronal noise, such as would be consistent with the concept of cortical hyperexcitability in migraine.
The two-dimensional (2D) trajectory of visual motion is usually not directly available to the visual system. Local one-dimensional (1D) sensors initiate processing but can only restrict the solution to a set of speed and direction combinations consistent with the 2D trajectory. These 1D signals are then integrated across orientation and space to compute 2D signals. Both motion integrations are thought to occur in higher cortical areas, but it remains unclear whether 1D signals are integrated over orientation and space simultaneously (1D pooling process), or instead are integrated locally with the resulting 2D signals then spatially integrated (2D pooling process). From psychophysical responses to novel global-motion stimuli comprised of numerous Gabor (1D) or Plaid (2D) elements, here we show that the human visual system adaptively switches between 1D pooling and 2D pooling depending on the input. When local 2D signals cannot be determined, the visual system shows effective 1D pooling that approximately follows the intersection of constraints rule. On the other hand, when local 2D signals are available, the visual system shows 2D pooling that approximately follows the vector average rule. Spatial motion integration therefore exhibits great flexibility when estimating complex optic flows in natural scenes.
The role of low-spatial-frequency information in the processing of global stimuli made up of local elements was examined. After selective removal of low spatial frequencies two major changes occurred in the pattern of results. First, response times to global stimuli were significantly slower and the usual speed advantage of global over local processing was lost. Second, when processing local features the usual decrease in response speed when the local and global letters are not the same (consistency effect) was not obtained. These effects could not be explained by changes in error rate, by contrast variation resulting from the process of filtering, or by loss of visual sensitivity due to greater eccentricity of global images.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.