On the relation between a green and bright window view and length of hospital stay in affective disorders.

Background: The salutary effect of window views on greenery for inpatients in hospitals on length of stay and recovery rate has been repeatedly shown, however, not for psychiatric inpatients. The study assessed the association between a window view on green trees or man-made objects and brightness of the room on length of stay in a sample of psychiatric inpatients from one clinic.

Methods: Data records of 244 psychiatric inpatients (mean age in years 41.

A comparison of the temporal and spatial properties of trans-saccadic perceptual recalibration and saccadic adaptation.

Repeated exposure to a consistent trans-saccadic step in the position of the saccadic target reliably produces a change of saccadic gain, a well-established trans-saccadic motor learning phenomenon known as saccadic adaptation. Trans-saccadic changes can also produce perceptual effects. Specifically, a systematic increase or decrease in the size of the object that is being foveated changes the perceptually equivalent size between fovea and periphery.

A generative learning model for saccade adaptation.

Plasticity in the oculomotor system ensures that saccadic eye movements reliably meet their visual goals-to bring regions of interest into foveal, high-acuity vision. Here, we present a comprehensive description of sensorimotor learning in saccades. We induced continuous adaptation of saccade amplitudes using a double-step paradigm, in which participants saccade to a peripheral target stimulus, which then undergoes a surreptitious, intra-saccadic shift (ISS) as the eyes are in flight.

Saccadic adaptation to a systematically varying disturbance.

Saccadic adaptation maintains the correct mapping between eye movements and their targets, yet the dynamics of saccadic gain changes in the presence of systematically varying disturbances has not been extensively studied. Here we assessed changes in the gain of saccade amplitudes induced by continuous and periodic postsaccadic visual feedback. Observers made saccades following a sequence of target steps either along the horizontal meridian (Two-way adaptation) or with unconstrained saccade directions (Global adaptation).

Effect of form cues on 1D and 2D motion pooling.

Local-motion information can provide either 1-dimensional (1D) or 2-dimensional (2D) solutions. 1D signals occur when the aperture problem has not been solved, so each signal is an estimate of the local-orthogonal component of the object's motion. 2D signals occur when the aperture problem has been solved, so each signal is an estimate of the object's motion.

Adaptation state of the local-motion-pooling units determines the nature of the motion aftereffect to transparent motion.

When observers adapt to a transparent-motion stimulus, the resulting motion aftereffect (MAE) is typically in the direction opposite to the vector average of the component directions. It has been proposed that the reason for this is that it is the adaptation state at the local-level (i.e.

No interaction of first- and second-order signals in the extraction of global-motion and optic-flow.

Edwards and Badcock (Vision Research 35, 2589, 1995) argued for independent first-order (FO) and second-order (SO) motion systems up to and including the global-motion level. That study used luminance (which they called FO) and contrast (SO) modulated dots. They found that SO noise dots did not mask signal extraction with luminance increment dots while luminance increment dots did mask SO signal extraction.

Frontal eye field neurons signal changes in decision criteria.

Flexible links between sensory stimuli and behavioral responses underlie many cognitive processes. One process that contributes to flexible decision-making is categorization. Some categories are innate or overlearned, but, in many cases, category boundaries represent flexible decision criteria that can shift on the fly to adapt to changes in the environment.

Neuronal responses to moving targets in monkey frontal eye fields.

Due to delays in visuomotor processing, eye movements directed toward moving targets must integrate both target position and velocity to be accurate. It is unknown where and how target velocity information is incorporated into the planning of rapid (saccadic) eye movements. We recorded the activity of neurons in frontal eye fields (FEFs) while monkeys made saccades to stationary and moving targets.

Visual remapping by vector subtraction: analysis of multiplicative gain field models.

Saccadic eye movements remain spatially accurate even when the target becomes invisible and the initial eye position is perturbed. The brain accomplishes this in part by remapping the remembered target location in retinal coordinates. The computation that underlies this visual remapping is approximated by vector subtraction: the original saccade vector is updated by subtracting the vector corresponding to the intervening eye movement.

Computing vector differences using a gain field-like mechanism in monkey frontal eye field.

Signals related to eye position are essential for visual perception and eye movements, and are powerful modulators of sensory responses in many regions of the visual and oculomotor systems. We show that visual and pre-saccadic responses of frontal eye field (FEF) neurons are modulated by initial eye position in a way suggestive of a multiplicative mechanism (gain field). Furthermore the slope of the eye position sensitivity tends to be negatively correlated with preferred retinal position across the population.

The neural representation of speed in macaque area MT/V5.

Tuning for speed is one key feature of motion-selective neurons in the middle temporal visual area of the macaque cortex (MT, or V5). The present paper asks whether speed is coded in a way that is invariant to the shape of the moving stimulus, and if so, how. When tested with single sine-wave gratings of different spatial and temporal frequencies, MT neurons show a continuum in the degree to which preferred speed depends on spatial frequency.