Perception – Visual Integration Task Name Description Motion Perception The paradigm measures cortical activations during visual motion perception, using fMRI. It provides assessments of both sensory and cognitive systems. fMRI Cognitive Construct Validity When the visual motion system is damaged, both perceptual and neural response to motion signals in primates will be deficient (Tootell et al., 1995). Neural Construct Validity When the visual motion system is damaged, both perceptual and neural response to motion signals in primates will be deficient (Tootell et al., 1995). Sensitivity to Manipulation Psilocybin impairs high-level but not low-level motion perception (Carter et al., 2004). Contrast detection is influenced by antipsychotic medications (Chen et al., 2003). (Chen et al., 2008) MANUSCRIPTS ON THE WEBSITE: Relationships to Behavior and Schizophrenia Application of this paradigm has indicated deficient as well excessive cortical responses to visual signals in schizophrenia patients (Chen et al., 2008; Chen, Nakayama, Levy, Matthysse, & Holzman, 1999). Psychometrics Stage of Research Not known There is evidence that this specific task elicits deficits in schizophrenia We need to assess psychometric characteristics such as test-retest reliability, practice effects, and ceiling/floor effects for this task. Chen, Y., Grossman, E. D., Bidwell, L. C., YurgelunTodd, D., Gruber, S. A., Levy, D. L., et al. (2008). Differential activation patterns of occipital and prefrontal cortices during motion processing: evidence from normal and schizophrenic brains. Cogn Affect Behav Neurosci, 8(3), 293-303. We have evidence that performance on this task changes in response to psychological or pharmacological intervention. Chen, Y., Palafox, G. P., Nakayama, K., Levy, D. L., Matthysse, S., & Holzman, P. S. (1999). Motion perception in schizophrenia. Arch Gen Psychiatry, 56(2), 149-154. Jittered Orientation Contour Integration Task (JOVI) fMRI In this test, participants are presented with stimuli and have to make a judgment as to whether an oval shape made up of separate Gabor elements is pointing to the left or the right. The orientation of the contour elements (tangent to the line 1) Various versions of this test have been validated in humans, where psychophysical manipulations of a single parameter (e.g., signalnoise, contour element orientation, etc) lead to predicted changes in task Data from patients, nonpatient human studies, and from monkey studies have shown that the test activates intermediate visual cortex regions, and that the degree of activation is strongly linked to the degree to which the integrity of the In a recent fMRI study (S. M. Silverstein et al., 2009), sensitivity of early visual cortex regions to the jitter manipulation (reduction in good continuation of the contour) was found in areas V1-V4, but not beyond (e.g., IT). Moreover, as predicted, Psychometric characteristics for both the behavioral and imaging version of this tasks are currently being examined. Practice effects (over There is evidence that this specific task elicits deficits in schizophrenia at both the behavioral and neural levels. We have some information on the or shape, and jittered to reduce perception of the contour) is manipulated across blocks of trials. Increasing jitter places increasing demands on visual integration mechanisms. (Kovacs, Kozma, Feher, & Benedek, 1999) (Kovacs, Polat, Pennefather, Chandna, & Norcia, 2000) (Kozma-Wiebe et al., 2006) (Pennefather, Chandna, Kovacs, Polat, & Norcia, 1999) (S. Silverstein et al., 2006; S. M. Silverstein et al., 2009) MANUSCRIPTS ON THE WEBSITE: Silverstein, S., Uhlhaas, P. J., Essex, B., Halpin, S., Schall, U., & Carr, V. (2006). Perceptual organization in first episode schizophrenia and ultra-high-risk states. Schizophrenia Research, 83(1), 41-52. Silverstein, S. M., Berten, S., Essex, B., Kovacs, I., Susmaras, T., & Little, D. M. (2009). An fMRI examination of visual integration in schizophrenia. J Integr Neurosci, 8(2), 175-202. . performance. 2) Test findings are consistent with models from computational neuroscience and theoretical neurobiology. 3) Findings using this task can not be accounted for in terms of attention, memory, or other cognitive factors. contour is altered: as jitter is increased slightly to moderately there are increases in activity as demand on integrative mechanisms is increased; however, once jitter increases to the point where the contour can no longer be perceived, activation level drops significantly. (Chandna, Pennefather, Kovacs, & Norcia, 2001) (Kiorpes & Bassin, 2003) (Kourtzi, Tolias, Altmann, Augath, & Logothetis, 2003) schizophrenia patients demonstrated reduced activation compared to controls in regions subserving integration, but not those involved in feature detection: there were no group differences in V1, but there were large differences in V2, V3, and V4. There were no group differences in higher areas such as IT. These data replicated earlier non-clinical human and monkey studies that used similar stimuli (but not with a 2AFC response format) and found the neural basis of contour integration to be primarily in V2 and V3 (LOC) (Altmann, Bülthoff, Kourtzi, 2003, Current Biology; Kourtzi, Tolias, Altmann, Augath, Logothetis, 2003, Neuron). 2, 3, and 4 days depending on the study) have been minimal in past studies by the Kovacs and Silverstein groups, and have not differed across control, schizophrenia and schizoaffective groups (Silverstein et al. 2006, Cognitive Neuropsychiatry). Test-retest reliability is currently being measured as part of the CNTRACS consortium project. Inter-rater reliability in healthy and amblyopic samples for detection thresholds was high, as reported in Pennefather et al. (1999, Spatial Vision). Ceiling and floor effects have not been demonstrated in fMRI data using the JOVI. The current version of the task has added conditions to the middle-difficulty range, to maximize power for betweengroup discriminations. Performance on this task also correlates negatively with performance on the Ebbinghaus illusion psychometric characteristics such as test-retest reliability, practice effects, and ceiling/floor effects for this task. We need to determine whether performance on this task changes in response to psychological or pharmacological intervention. Kanisza Square Illusion fMRI Parametric modulation of perceptual grouping using the Kanisza square illusion in an imaging paradigm that probes the degree of sensory interactions among multiple stimuli. (Beck & Kastner, 2005; McMains & Kastner, 2010) MANUSCRIPTS ON THE WEBSITE: Beck, D. M., & Kastner, S. (2005). Stimulus context modulates competition in human extrastriate cortex. Nat Neurosci, 8(8), 11101116. McMains, S. A., & Kastner, S. (2010). Defining the units of competition: influences of perceptual organization on competitive interactions in human visual cortex. J Cogn Neurosci, 22(11), 2417-2426. The representation of visual information in cortex depends strongly on the degree to which stimuli compete with each other. This neural competition is an automatic process. However, it has been shown to provide an important neural principle for attentional selection to operate on (e.g. Duncan's & Desimone's biased competition theory). In the proposed paradigm we have investigated the influences of bottom-up factors in the form of perceptual grouping on the level of competition. This paradigm informs about the integrity of perceptual mechanisms in visual cortex. The representation of visual information in cortex depends strongly on the degree to which stimuli compete with each other. This neural competition is an automatic process. However, it has been shown to provide an important neural principle for attentional selection to operate on (e.g. Duncan's & Desimone's biased competition theory). In the proposed paradigm we have investigated the influences of bottom-up factors in the form of perceptual grouping on the level of competition. This paradigm informs about the integrity of perceptual mechanisms in visual cortex (Beck & Kastner, 2005; McMains & Kastner, 2010). Unknown This paradigm looks at two automatic processes that shape how we perceive the world: neural competition and perceptual grouping in visual cortex. There is evidence that perceptual organization is impaired in schizophrenia. task, in which a visual integration deficit leads to a reduced contextbased illusion supporting the hypothesis that scores do not reflect a generalized deficit (Uhlhaas et al. 2006, Perceptual grouping in disorganized schizophrenia. Schizophrenia Research, 145, 105117). Both paradigms have been used in several published papers, and they are very robust. Subjects simply maintain fixation, since we measure automatic processes (i.e. no practice, ceiling effects and the like). There is evidence that similar tasks elicit deficits in schizophrenia at the behavioral and neural level. We need to assess psychometric characteristics such as test-retest reliability, practice effects, and ceiling/floor effects for the imaging and behavioral data. We need to study whether or not performance on this task changes in response to psychological or pharmacological intervention. REFERENCES: Beck, D. M., & Kastner, S. (2005). Stimulus context modulates competition in human extrastriate cortex. Nat Neurosci, 8(8), 1110-1116. Carter, O. L., Pettigrew, J. D., Burr, D. C., Alais, D., Hasler, F., & Vollenweider, F. X. (2004). Psilocybin impairs high-level but not low-level motion perception. Neuroreport, 15(12), 1947-1951. Chandna, A., Pennefather, P. M., Kovacs, I., & Norcia, A. M. (2001). Contour integration deficits in anisometropic amblyopia. Invest Ophthalmol Vis Sci, 42(3), 875-878. Chen, Y., Grossman, E. D., Bidwell, L. C., Yurgelun-Todd, D., Gruber, S. A., Levy, D. L., et al. (2008). Differential activation patterns of occipital and prefrontal cortices during motion processing: evidence from normal and schizophrenic brains. Cogn Affect Behav Neurosci, 8(3), 293-303. Chen, Y., Levy, D. L., Sheremata, S., Nakayama, K., Matthysse, S., & Holzman, P. S. (2003). Effects of typical, atypical, and no antipsychotic drugs on visual contrast detection in schizophrenia. Am J Psychiatry, 160(10), 1795-1801. Chen, Y., Nakayama, K., Levy, D. L., Matthysse, S., & Holzman, P. S. (1999). Psychophysical isolation of a motion-processing deficit in schizophrenics and their relatives and its association with impaired smooth pursuit. Proc Natl Acad Sci U S A, 96(8), 4724-4729. Kiorpes, L., & Bassin, S. A. (2003). Development of contour integration in macaque monkeys. Vis Neurosci, 20(5), 567-575. Kourtzi, Z., Tolias, A. S., Altmann, C. F., Augath, M., & Logothetis, N. K. (2003). Integration of local features into global shapes: monkey and human FMRI studies. Neuron, 37(2), 333-346. Kovacs, I., Kozma, P., Feher, A., & Benedek, G. (1999). Late maturation of visual spatial integration in humans. Proceedings of the National Academy of Sciences, 96, 12204-12209. Kovacs, I., Polat, U., Pennefather, P. M., Chandna, A., & Norcia, A. M. (2000). A new test of contour integration deficits in patients with a history of disrupted binocular experience during visual development. Vision Res, 40(13), 1775-1783. Kozma-Wiebe, P., Silverstein, S., Feher, A., Kovacs, I., Ulhaas, P., & Wilkniss, S. (2006). Development of a Word-Wide Web based contour integration test: Reliablity and validity. Computers in Human Behavior, 22, 971-980. McMains, S. A., & Kastner, S. (2010). 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