Recycling of Nutrients from Dairy Wastewater by Extremophilic Microalgae with High Ammonia Tolerance.

This study explored the possibility of incorporating extremophilic algal cultivation into dairy wastewater treatment by characterizing a unique algal strain. Results showed that extremophilic microalgae CA1 newly isolated from dairy wastewater tolerated a high level of ammonia nitrogen (2.7 g/L), which was over 20 times the ammonia nitrogen that regular sp.

Blindsight after hemidecortication: visual stimuli in blind hemifield influence anti-saccades directed there.

Patients missing a cortical hemisphere, removed surgically at adulthood, cannot consciously see a visual probe stimulus (P) flashed in their blind contralesional, hemifield. Nevertheless, they have a low-level form of blindsight wherein P can affect the reaction time of a manual response to the appearance of a visual target in their seeing hemifield. This ability is thought to require the pathway from retina-to-ipsilesional superior colliculus (SC) to cortex of the remaining hemisphere (Leh et al.

Ipsilateral head and centring eye movements evoked from monkey premotor cortex.

Recent studies in monkeys have identified a 'polysensory, defensive zone', in the ventral premotor cortex, stimulation of which results in coordinated multisegmental movements reminiscent of those normally produced by animals that react to head-directed threatening stimuli. Here, we describe gaze movements evoked in the head-fixed and head-unrestrained monkey by electrical stimulation of the polysensory zone. Centring eye movements were elicited at all sites and under both conditions.

Evidence for gaze feedback to the cat superior colliculus: discharges reflect gaze trajectory perturbations.

Rapid coordinated eye-head movements, called saccadic gaze shifts, displace the line of sight from one location to another. A critical structure in the gaze control circuitry is the superior colliculus (SC) of the midbrain, which drives gaze saccades by relaying cortical commands to brainstem eye and head motor circuits. We proposed that the SC lies within a gaze feedback loop and generates an error signal specifying gaze position error (GPE), the distance between target and current gaze positions.

On the feedback control of orienting gaze shifts made with eye and head movements.

Combined eye-head movements are routinely used to orient the visual axis (gaze) rapidly in space. The gaze control system can be modeled using a feedback system in which an internally created instantaneous gaze position error signal equivalent to the distance between the target and the current gaze position is used to drive brainstem eye and head motor circuits. The visual axis is driven until this gaze position error (GPE) is zero.

Superior colliculus encodes distance to target, not saccade amplitude, in multi-step gaze shifts.

The superior colliculus (SC) is important for generating coordinated eye-head gaze saccades. Its deeper layers contain a retinotopically organized motor map in which each site is thought to encode a specific gaze saccade vector. Here we show that this fundamental assumption in current models of collicular function does not hold true during horizontal multi-step gaze shifts in darkness that are directed to a goal and composed of a sequence of gaze saccades separated by periods of steady fixation.

In multiple-step gaze shifts: omnipause (OPNs) and collicular fixation neurons encode gaze position error; OPNs gate saccades.

The superior colliculus (SC), via its projections to the pons, is a critical structure for driving rapid orienting movements of the visual axis, called gaze saccades, composed of coordinated eye-head movements. The SC contains a motor map that encodes small saccade vectors rostrally and large ones caudally. A zone in the rostral pole may have a different function.