Perceptual learning is an instance of adult plasticity whereby training in a sensory (e.g., a visual task) results in neuronal changes leading to an improved ability to perform the task. Yet studies in primary visual cortex have found that changes in neuronal response properties were relatively modest. The present study examines the effects of training in an orientation discrimination task on the response properties of V4 neurons in awake rhesus monkeys. Results indicate that the changes induced in V4 are indeed larger than those in V1. Nonspecific effects of training included a decrease in response variance, and an increase in overall orientation selectivity in V4. The orientation-specific changes involved a local steepening in the orientation tuning curve around the trained orientation that selectively improved orientation discriminability at the trained orientation. Moreover, these changes were largely confined to the population of neurons whose orientation tuning was optimal for signaling small differences in orientation at the trained orientation. Finally, the modifications were restricted to the part of the tuning curve close to the trained orientation. Thus, we conclude that it is the most informative V4 neurons, those most directly involved in the discrimination, that are specifically modified by perceptual learning.

We used gratings and shapes defined by relative motion to study selectivity for static kinetic boundaries in macaque V4 neurons. Kinetic gratings were generated by random pixels moving in opposite directions in the neighboring bars, either parallel to the orientation of the boundary (parallel kinetic grating) or perpendicular to the boundary (orthogonal kinetic grating). Neurons were also tested with static, luminance defined gratings to establish cue invariance. In addition, we used eight shapes defined either by relative motion or by luminance contrast, as used previously to test cue invariance in the infero-temporal (IT) cortex. A sizeable fraction (10-20%) of the V4 neurons responded selectively to kinetic patterns. Most neurons selective for kinetic contours had receptive fields (RFs) within the central 10 degrees of the visual field. Neurons selective for the orientation of kinetic gratings were defined as having similar orientation preferences for the two types of kinetic gratings, and the vast majority of these neurons also retained the same orientation preference for luminance defined gratings. Also, kinetic shape selective neurons had similar shape preferences when the shape was defined by relative motion or by luminance contrast, showing a cue-invariant form processing in V4. Although shape selectivity was weaker in V4 than what has been reported in the IT cortex, cue invariance was similar in the two areas, suggesting that invariance for luminance and motion cues of IT originates in V4. The neurons selective for kinetic patterns tended to be clustered within dorsal V4.

Motion is a potent cue for breaking camouflage in the natural world. To understand the neural basis of this phenomenon, one must utilize moving shapes defined by coherent motion of random texture elements against a similar, but stationary texture. To investigate how well neurons in area V4 process this novel, ecologically relevant stimulus and to compare shape selectivity for these shapes with static and other moving shapes, we tested V4 neurons with 5 static or moving shapes defined either by luminance or kinetic cues. The kinetic cues included a temporal frequency cue due to the difference in temporal frequencies of the moving dots inside the shape boundary and stationary dots outside the boundary. Therefore, static opponent motion-defined shapes without this cue were tested as an additional control. Approximately 44% (95/216) of V4 neurons showed shape selectivity. Analyses of these selective neurons both at single-neuron and population levels revealed that the shape-selective V4 neurons responded selectively to the moving kinetic shapes and that these neurons demonstrated robust invariance for shape preference across different shape conditions. Cue-invariant shape selectivity was more pronounced when kinetic shapes included the temporal frequency cue. This invariance may be rooted in nonlinearities occurring early in the visual pathway.

Motion is a potent cue for the perception of three-dimensional (3D) shape in primates, but little is known about its underlying neural mechanisms. Guided by recent functional magnetic resonance imaging results, we tested neurons in the fundus of the superior temporal sulcus (FST) area of two macaque monkeys (Macaca mulatta, one male) using motion-defined surface patches with various 3D shapes such as slanted planes, saddles, or cylinders. The majority of the FST neurons (Ͼ80%) were selective for stimuli depicting specific shapes, and all the surfaces tested were represented among the selective FST neurons. Importantly, this selectivity tolerated changes in speed, position, size, or between binocular and monocular presentations. This tolerance demonstrates that the 3D structure-from-motion (3D-SFM) selectivity of FST neurons is a higher-order selectivity, which cannot be reduced to a lower-order speed selectivity. The 3D-SFM selectivity of FST neurons was unaffected by removal of the opposed-motion cue that supplemented the speed gradient cue in the standard stimuli. When tested with the same standard stimuli, fewer neurons in the middle temporal/visual 5 (MT/V5) area were selective than FST neurons. In addition, selective MT/V5 neurons represented fewer types of surfaces and were less tolerant of stimulus changes than FST neurons. Overall, these results indicate that FST neurons code motion-defined 3D shape fragments, underscoring the central role of FST in processing 3D-SFM.

ObjectiveThe Open Researcher and Contributor ID identifier (ORCID iD) is a unique code for crediting researchers and a useful tool allowing organizations to track and report on their research. ORCID has been adopted across academia and some journals now require ORCID iDs from authors at submission. Pharmaceutical industry engagement with ORCID has been limited, but increasing numbers of employees are registering.Open Pharma, which brings together industry, publishers and other healthcare stakeholders to improve the model of medical publishing, recognized ORCID as an important innovation.Being an Open Pharma participant, GSK Vaccines initiated a pilot study to assess the feasibility of implementing ORCID and to encourage internal authors to register for ORCID iDs. Research design and methodsInternal authors were educated about ORCID and Open Pharma via a newsletter and user guide. They were asked to confirm registration with ORCID through Datavision™ (from 14/08/2017 onwards). Unsolicited feedback was recorded. ResultsOn 13/12/2017, 328 of 531 internal authors (62%) had registered with ORCID. Datavision ™ enabled ORCID iD collection and extraction of a report of those who had registered.Unsolicited comments (n=24) mostly related to technical issues and were adequately resolved. A few individuals enquired about easier ways to link their ORCID iD with their previous publications.