411,345 research outputs found

    Dummy eye measurements of microsaccades: testing the influence of system noise and head movements on microsaccade detection in a popular video-based eye tracker

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    Whereas early studies of microsaccades have predominantly relied on custom-built eye trackers and manual tagging of microsaccades, more recent work tends to use video-based eye tracking and automated algorithms for microsaccade detection. While data from these newer studies suggest that microsaccades can be reliably detected with video-based systems, this has not been systematically evaluated. I here present a method and data examining microsaccade detection in an often used video-based system (the Eyelink II system) and a commonly used detection algorithm (Engbert & Kliegl, 2003; Engbert & Mergenthaler, 2006). Recordings from human participants and those obtained using a pair of dummy eyes, mounted on a pair of glasses either worn by a human participant (i.e., with head motion) or a dummy head (no head motion) were compared. Three experiments were conducted. The first experiment suggests that when microsaccade measurements make use of the pupil detection mode, microsaccade detections in the absence of eye movements are sparse in the absence of head movements, but frequent with head movements (despite the use of a chin rest). A second experiment demonstrates that by using measurements that rely on a combination of corneal reflection and pupil detection, false microsaccade detections can be largely avoided as long as a binocular criterion is used. A third experiment examines whether past results may have been affected by possible incorrect detections due to small head movements. It shows that despite the many detections due to head movements, the typical modulation of microsaccade rate after stimulus onset is found only when recording from the participants’ eyes

    Spectral and ocellar inputs to honeybee motion-sensitive descending neurons

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    Optomotor reflexes have been observed in many insects and in some cases the neural pathways that mediate these reflexes have been identified physiologically and anatomically. In honeybees Kaiser (1975) established that the spectral sensitivity of optomotor responses in bees almost exactly matched that of the green photoreceptors, suggesting an exclusive input from green photoreceptors. However, physiological studies showed that the motion detectors in the optic lobes have a secondary response peak in the UV region of the spectrum suggesting that there may be more than one type of photoreceptor involved in the optomotor response. Thus in this thesis, I investigate the neural basis of motion and spectral wavelength processing in motion-sensitive descending neurons, which are on the optomotor response pathway, to reveal the neural contributions from other spectral receptor types. In this study, intracellular recording techniques were utilised. The stimuli consisted of a wide-field LED (light emitting diode) display in which green (peak 530 nm) and short-wavelength (peak 380 nm) LEDs were mounted in pairs across a wide visual area. Six types of motion-sensitive descending neurons were recorded and anatomically identified, including two pitch-sensitive neurons (Locth3, DNII2), two roll-sensitive neurons (DNIV2 and DNIV3) and two yaw-sensitive neurons (DNVII1 and DNVII2). The results show that for the vertical sensitive (pitch and roll) neurons, the cells have equal-sized excitatory responses to motion when using short-wavelength or green motion stimulation. However, for the horizontal sensitive (yaw-sensitive) neurons excitatory responses only occurred for the green stimulus in the preferred direction. The short-wavelength stimulus induced clear inhibitory responses for all tested motion directions. The results suggest that besides green photoreceptors, the motion-sensitive descending neurons also receive inputs from the short-wavelength photoreceptors, but only for motion detectors tuned for vertical motion. Honeybees, like most flying insects, have three ocelli (simple eyes) located on the top of the head, in addition to the compound eyes. However, the exact function of the bee ocelli and the information computation between the ocelli, compound eyes and central brain remain unclear. In this thesis, I investigate the ocellar properties morphologically, anatomically and physiologically. Semi-thin sections and focal length measurements were performed on both median and lateral ocelli, a 3-dimensional reconstruction model of the honeybee ocellar lenses and retinas was developed to understand the visual fields of the ocelli. Intracellular electrophysiology experiments were carried out on descending neurons to understand the information processing between the ocelli and compound eyes. Cell responses to different stimuli were recorded with and without the ocelli covered. It is shown that the ocellar input provides a faster response to motion stimuli than with compound eye stimulation alone, and also increases the amplitude of responses to flashed stimuli. In the case of the DNII2 neuron, it is also shown that the ocelli provide a directional contribution to the responses

    The Practice of the Circle

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    I. Recognition. Drawing the Circle The metaphor of the circle is here taken into account as a typifying image of the Emersonian moral. In this paper I shall attempt to provide an explanatory synthesis of the concept of “circle,” in its acceptation as “the outlined,” “path,” “itinerary.” The circle will be not investigated as a mere geometrical figure, but as a condition of motion, an occasion of processuality. It will be presented as a route which unravels itself before the subject’s eyes and..

    I can see it in your eyes: what the Xenopus laevis eye can teach us about motion perception

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