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Rowley, D. P.

Publications and source records attributed to Rowley, D. P..

6 recordsLinked to original sources

Active sensing explains cortical variability and improves visual information

Active vision is often considered at the scale of saccades, with each fixation treated as a static visual sample. Yet the eyes continue to move during fixation, continually transforming the retinal input. Here we measured these movements at high precision while recording neuronal populations in the foveal primary visual cortex of awake marmosets viewing repeated flashed natural images. Fixational eye movements accounted for most conditional firing-rate variability and nearly all shared variability not explained by the trial-averaged response. An image-computable model captured this modulation largely from gaze-dependent retinal input; explicit eye-position and eye-velocity signals added little predictive power. Under natural viewing, retinal motion redistributed image power across temporal frequencies, and motion effects grew when this power engaged spatiotemporal tuning. In model-derived populations, fixational motion increased the spatial information carried per spike relative to stabilized input, with sharpening growing across successive nonlinear stages. Thus, activity commonly assigned to cortical noise is not just structured visual reafference generated by the movement of the observer, but is beneficial signal which sharpens spatial representations.

neuroscience↗

Systemic AAV delivery of a calcium indicator in marmosets: functional validation in visual area MT

Functional optical imaging in nonhuman primates provides an important complement to electrophysiological approaches in neuroscience research, but its broader use has been limited by challenges in achieving large-scale, homogeneous expression of genetically encoded reporters, and imaging accessibility in species with gyrencephalic brains with sulci and fissures (e.g., rhesus macaques). Specifically, conventional local intracortical viral injections are invasive and often produce spatially restricted or heterogeneous expression, constraining population-level analyses. Here, we show that systemic intravenous delivery of an adeno-associated virus (AAV) capsid engineered for enhanced blood-brain barrier crossing, AAV.CAP-B10, supports robust and widespread expression of a calcium indicator CAaMP8s in the common marmoset. Intravenous delivery in two marmosets resulted in widespread cortical expression. Using a large cranial window over extrastriate visual area MT (and its satellite areas), we performed widefield single-photon imaging and two-photon cellular-resolution imaging in awake,behaving marmosets to functionally validate activity in this well studied primate visual-motion sensitive cortical area. Population level responses to visual motion and spatial organization measured with widefield imaging, as well as single-cell level motion direction tuning measured with two-photon imaging, were consistent with canonical properties of MT reported in previous electrophysiological studies. Quantitative analyses of lightsheet imaging after whole hemisphere brain clearing further confirmed the broad expression of GCaMP in both cortical and subcortical areas. Together, these results indicate that systemic delivery using AAV.CAP-B10 provides a minimally invasive approach for robust multi-scale functional optical imaging in awake, behaving marmosets.

neuroscience↗

Structural and functional evidence supports re-defining mouse higher order visual areas into a single area V2

The mouse has become one of the main organisms for studies of the visual system. As a result, there is increased effort to understand universal principles of visual processing by comparing the mouse visual system to that of other species. In primates and other well-studied species including cats and tree shrews, the visual cortex is parcellated into an area V1 and several higher order areas defined by structural and functional differences, and a near complete map of the visual field. In mice, the visual cortex beyond V1 is parcellated into several higher order areas, with less notable structural and functional differences, partial coverage of the visual field, and areal boundaries defined by reversals in progression of the visual field. Notably, recent work in tree shrews and primates has shown that reversals in progression of the visual field can be a hallmark of complex retinotopic mapping within a single visual area. This, and other lines of evidence discussed here, provides a compelling case that the apparent existence of multiple higher order visual areas in the mouse is related to the false assumption of simple retinotopy. Specifically, we use simulations to show that complex retinotopy within a single visual area can recapitulate the appearance of multiple areal borders beyond mouse V1. In addition, we show that many reported differences in functional properties between higher order visual areas can be better explained by retinotopic differences rather than areal identity. Our proposal to reclassify some of the higher order visual areas in the mouse into a single area V2 is not mere semantics because areal definitions influence experimental design and data analysis. Furthermore, such a reclassification would produce a common set of rules for defining areal boundaries among mammals and would bring the mouse visual system into agreement with evolutionary evidence for a single area V2 in related lineages.

neuroscience↗

Activity in the peripheral representation within primate V1 is substantially modulated during running

We recently investigated whether activity in primary visual cortex of a primate (Callithrix jacchus) is modulated during running, and found that the effects were small (and suppressive), a notable difference from the large and positive modulations observed in mice. In that first report, we noted that the majority of our data were collected from the retinotopic representation of the fovea, and surmised that running modulations might be different in the peripheral representation. Here, we report that running-correlated modulations of the peripheral representation in marmoset V1 are positive and substantial-- on order of 30%. In light of both the small and negative modulations observed in foveal V1, and the large and positive modulations seen in mouse V1, these results suggest that the foveal representation in primates may be unique. In this domain, non-foveal V1 in primates appears more similar to that of rodents.

neuroscience↗

Running modulates primate and rodent visual cortex via common mechanism but quantitatively distinct implementation

When mice run, activity in their primary visual cortex (V1) is strongly modulated. This observation has altered conceptions of a brain region assumed to be a passive image processor. Extensive work has followed to dissect the circuits and functions of running-correlated modulation. However, it remains unclear whether visual processing in primates might similarly change during locomotion. We therefore measured V1 activity in marmosets while they viewed stimuli on a treadmill. In contrast to mouse, running-correlated modulations of marmoset V1 were small, and tended to be slightly suppressive. Population-level analyses revealed trial- to-trial fluctuations of shared gain across V1 in both species, but while strongly correlated with running in mice, gain modulations were smaller and more often negatively correlated with running in marmosets. Thus, population-wide fluctuations of V1 may reflect a common feature of mammalian visual cortical function, but important quantitative differences point to distinct consequences for the relation between vision and action in primates versus rodents.

neuroscience↗

A \"twisted\" visual field map in the primate cortex predicted by topographic continuity

Adjacent neurons in visual cortex have overlapping receptive fields within and across area boundaries, an arrangement which is theorized to minimize wiring cost. This constraint is thought to create retinotopic maps of opposing field sign (mirror and non-mirror representations of the visual field) in adjacent visual areas, a concept which has become central in current attempts to subdivide the cortex. We modelled a realistic developmental scenario in which adjacent areas do not mature simultaneously, but need to maintain topographic continuity across their borders. This showed that the same mechanism that is hypothesized to maintain topographic continuity within each area can lead to a more complex type of retinotopic map, consisting of sectors with opposing field sign within a same area. Using fully quantitative electrode array recordings, we then demonstrate that this type of map exists in the primate extrastriate cortex.

neuroscience↗