2014
DOI: 10.1152/jn.00254.2013
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Integration and segregation of multiple motion signals by neurons in area MT of primate

Abstract: McDonald JS, Clifford CW, Solomon SS, Chen SC, Solomon SG. Integration and segregation of multiple motion signals by neurons in area MT of primate.

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Cited by 53 publications
(58 citation statements)
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References 32 publications
(52 reference statements)
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“…This is consistent with the distribution of likelihood (Graf et al 2011;Jazayeri and Movshon 2006) or Fisher information (Tzvetanov and Womelsdorf 2008) across the neural population. Similar "flank-encoding" representations have been implicated in the discrimination of other visual features: spatial frequency (Bradley et al 1987), orientation (Beaudot and Mullen 2006;Graf et al 2011;Paradiso 1988;Pouget and Thorpe 1991), and motion direction (McDonald et al 2014;Purushothaman and Bradley 2005;Seung and Sompolinsky 1993;Tzvetanov and Womelsdorf 2008).…”
Section: Discussionmentioning
confidence: 86%
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“…This is consistent with the distribution of likelihood (Graf et al 2011;Jazayeri and Movshon 2006) or Fisher information (Tzvetanov and Womelsdorf 2008) across the neural population. Similar "flank-encoding" representations have been implicated in the discrimination of other visual features: spatial frequency (Bradley et al 1987), orientation (Beaudot and Mullen 2006;Graf et al 2011;Paradiso 1988;Pouget and Thorpe 1991), and motion direction (McDonald et al 2014;Purushothaman and Bradley 2005;Seung and Sompolinsky 1993;Tzvetanov and Womelsdorf 2008).…”
Section: Discussionmentioning
confidence: 86%
“…The reduced resolution in periphery reflects an increase in average receptive-field size from of 6.3°to 11.7°. In a separate recording from the same animals, we estimated the directional tuning of multiunit activity for a field of moving dots (McDonald et al 2014). Full-width, half-maximum directional tuning bandwidth was an angular 130°(Ϯ54 SD) and was similar for neurons with parafoveal and peripheral receptive fields (P ϭ 0.10, t-test); a commonly used index of directional selectivity (1 Ϫ resp null /resp pref ) in the same recordings was 0.81 (Ϯ0.34 SD).…”
Section: Resultsmentioning
confidence: 99%
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“…A few previous studies have examined interactions between visual motion patterns that simulate self-motion and object motion in area MSTd (Logan and Duffy, 2006;Sato et al, 2010;Kishore et al, 2012). These studies show that MSTd responses depend on self-motion and object motion in complex ways, but they did not systematically explore the joint tuning of MSTd neurons for heading and object direction, nor how nonvisual inputs influence the joint representation of self-motion and object motion.…”
Section: Introductionmentioning
confidence: 99%