36 research outputs found

    Auditory cortical responses in the cat to sounds that produce spatial illusions

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    Humans and cats can localize a sound source accurately if its spectrum is fairly broad and flat(1-3), as is typical of most natural sounds. However, if sounds are filtered to reduce the width of the spectrum, they result:in illusions of sources that are very different from the actual locations, particularly in the up/down and front/back dimensions(4-6). Such illusions reveal that the auditory system relies on specific characteristics of sound spectra to obtain cues for localization(7). In the-auditory cortex of cats, temporal firing patterns of neurons can signal the locations of broad-band sounds(8-9). Here we show that such spike patterns systematically mislocalize sounds that have been passed through a narrow-band filter. Both correct and incorrect locations signalled by neurons can be predicted quantitatively by a model of spectral processing that also predicts correct and incorrect localization judgements by human listeners(6). Similar cortical mechanisms, if present in humans, could underlie human auditory spatial perception.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/62778/1/399688a0.pd

    Cortical areas involved in object, background, and object-background processing revealed with functional magnetic resonance adaptation

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    Telah dilakukan penelitian terhadap modifikasi kristal Tolbutamida untuk memperoleh suatu bentuk kristal dengan kelarutan tertinggi atau lebih dikenal struktur kristal aktif. Modifikasi kristal diperoleh dengan menggunakan bermacam macam pelarut (polar non polar) dan bervariasinya kecepatan pendinginan. Analisa kristal didasarkan pada spektra infra merah, analisa termal (differential thermal Analysis dan Thermo gravi metri analysis). difraksi sinar-X dan kelarutan

    A continuous dynamic beam model for swimming fish

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    When a fish swims in water, muscle contraction, controlled by the nervous system, interacts with the body tissues and the surrounding fluid to yield the observed movement pattern of the body. A continuous dynamic beam model describing the bending moment balance on the body for such an interaction during swimming has been established. In the model a linear visco-elastic assumption is made for the passive behaviour of internal tissues, skin and backbone, and the unsteady fluid force acting on the swimming body is calculated by the 3D waving plate theory. The body bending moment distribution due to the various components, in isolation and acting together, is analysed. The analysis is based on the saithe (Pollachius virens), a carangiform swimmer. The fluid reaction needs a bending moment of increasing amplitude towards the tail and near-standing wave behaviour on the rear-half of the body. The inertial movement of the fish results from a wave of bending moment with increasing amplitude along the body and a higher propagation speed than that of body bending. In particular, the fluid reaction, mainly designed for propulsion, can provide a considerable force to balance the local momentum change of the body and thereby reduce the power required from the muscle. The wave of passive visco-elastic bending moment, with an amplitude distribution peaking a little before the mid-point of the fish, travels with a speed close to that of body bending. The calculated muscle bending moment from the whole dynamic system has a wave speed almost the same as that observed for EMG-onset and a starting instant close to that of muscle activation, suggesting a consistent matching between the muscle activation pattern and the dynamic response of the system in steady swimming. A faster wave of muscle activation, with a variable phase relation between the strain and activation cycle, appears to be designed to fit the fluid reaction and, to a lesser extent, the body inertia, and is limited by the passive internal tissues. Higher active stress is required from caudal muscle, as predicted from experimental studies on fish muscle. In general, the active force development by muscle does not coincide with the propulsive force generation on the tail. The stiffer backbone may play a role in transmitting force and deformation to maintain and adjust the movement of the body and tail in water
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