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Mohr, K. S.

Publications and source records attributed to Mohr, K. S..

3 recordsLinked to original sources

Neurally-Informed Models of Protracted Sequential Sampling of Long, Noise-free Stimuli

Perceptual decision behaviour is known to be well-captured by models based on sequential sampling and temporal integration, but doubts have been raised about the generality and identifiability of these operations. Here we used neurally-constrained modelling to probe their role and temporal extent in the uncertain case of perceptual judgments about long-duration stimuli with no physical noise but weak evidence. We found that accuracy steadily improved across four covertly-manipulated evidence durations, indicating protracted sampling, but these delayed behavioural reports alone were insufficient to establish the operation of integration or of a decision-terminating bound. We then elaborated the models to prescribe how they would generate decision variable signals as well as choices, and fit them additionally to the average dynamics of a centroparietal electroencephalographic signal ( CPP) that traces decision formation. This established the setting of a bound and ruled out some non-integration mechanisms. However, one extrema detection model, which evokes a stereotyped signal flagging the first bound-exceeding sample, rivalled the integration model in reproducing the evidence-dependent buildup dynamics of the CPP, alongside behavioural data. Moreover, the two models captured different features of neural motor preparation signals but neither captured all of them. We discuss the implications for the generality of integration and the technical challenges of neurally-informed modelling given limited behavioural data.

neuroscience↗

Readout and delayed transmission of initial afferent V1 activity in decisions about stimulus contrast

Initial afferent activation of V1, indexed by the C1 component of the human VEP, is often considered to be a rudimentary stage of visual processing, operating mostly as a conduit for later stages with limited cognitive penetrability. The full suite of visual analysis entails activity across several visual areas and feedback from later areas to earlier ones. This raises the question of whether the early sensory representation indexed by the C1 is read out for perceptual decisions or whether it is passed over in favour of more advanced representations. To address this question, we asked whether the C1 would predict time-pressured stimulus contrast comparisons independently of physical stimulus conditions, a phenomenon known as choice probability. We found that the C1 did this for a narrow range of response times, indicative of decision readout since the C1 is a transient signal. This effect could not be accounted for by stimulus differences, choice history, or any other choice-predictive signal that we could identify in either the time or frequency domain, either before or after target onset. It also preceded the onset of evidence-dependent decision formation estimated from the centroparietal positivity by tens of milliseconds, together providing an approximate timeline of early evidence readout and its delayed impact on the decision.

neuroscience↗

Visual cortical area contributions to the transient, multifocal and steady-state VEP: A forward model-informed analysis

Central to our understanding of how visual evoked potentials (VEPs) contribute to visual processing is the question of where their anatomical sources are. Three well-established measures of low-level visual cortical activity are widely used: the first component ("C1") of the transient and multifocal VEP, and the steady-state VEP (SSVEP). Although primary visual cortex (V1) activity has often been implicated in the generation of all three signals, their dominant sources remain uncertain due to the limited resolution and methodological heterogeneity of source modelling. Here, we provide the first characterisation of all three signals in one analytic framework centred on the cruciform model, which describes how scalp topographies of V1 activity vary with stimulus location due to the retinotopy and unique folding pattern of V1. We measured the transient C1, multifocal C1, and SSVEPs driven by an 18.75Hz and 7.5Hz flicker, and regressed them against forward-models of areas V1, V2 and V3 generated from the Benson-2014 retinotopy atlas. The topographic variations of all four VEP signals across the visual field were better captured by V1 models, explaining between 2-6 times more variance than V2/V3. Models with all three visual areas improved fit further, but complementary analyses of temporal dynamics across all three signals indicated that the bulk of extrastriate contributions occur considerably later than V1. Overall, our data support the use of peak C1 amplitude and SSVEPs to probe V1 activity, although the SSVEP contains stronger extrastriate contributions. Moreover, we provide elaborated heuristics to distinguish visual areas in VEP data based on signal lateralization as well as polarity inversion.

neuroscience↗