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Animal Motion Perception

Most animals move around in their environment, and through evolutionary time, this has resulted in specializations in their sensory systems and brains, to detect motion, as described in this entry. These patterns of movement can occur as moving images in vision, as moving sounds in hearing, and as moving tactile patterns in touch. Visual motion can be simply divided into two classes; the first, called object motion, is produced when some object moves relative to stationary objects in the world. The second class of motion, called self-motion, is produced by the observing animal itself moving its body, head, or eyes and thereby creating movement of the entire image across its visual field.

Although visual object motion can be produced by nonliving things such as rain, snow, leaves, waves, or clouds, most visual object motion is produced by the movement of other animals. It is advantageous for an animal to notice the movement of other animals because other animals may be the viewing animal's prey, a predator, or one of its own species and detecting them will greatly help the animal capture prey, avoid predators, and engage in social interactions, respectively. The other distinctive class of motion patterns is produced by an animal itself moving through a world of stationary objects, and these visual “flow patterns” are used to control its own movements, steer through space, obtain depth information through motion parallax, avoid obstacles, and even help maintain its posture and balance. Not surprisingly, there are separate areas of the visual system to process moving objects and self-produced motion patterns, which in turn generate distinctive behavioral responses, and they are found in both invertebrates and vertebrates alike.

Visual Neurons

Early research on frogs and insects showed that some visual neurons were specialized to respond only to relatively small moving visual stimuli, and often these preferred a particular direction of motion. These directional specific neurons were sequence detectors. If two adjacent areas in the visual field (say A and B) were stimulated by a moving stimulus that moved over A then B, the neuron would fire to signal this event. However, if the direction were reversed so that B then A was stimulated, the neuron would not fire, but would be inhibited. Early experiments showed that two flashed stimuli one at A and then the next at B after a short delay, also stimulated these movement neurons, but again, they did not fire when B then A were flashed without movement. Thus, these neurons respond to apparent motion as well as real motion. These motion-detecting neurons that respond to small moving things are precisely the stimuli that capture an animal's attention and typically produce a turning of the head and eyes (“orienting response”) to place the object's image onto the fovea or retinal area of high resolution. In frogs, these were nicknamed “Bug Detectors” because frogs turn and snap at bug-like moving patterns. Typically, larger moving stimuli produce escape or avoidance behavior in animals.

Movement and direction-specific neurons have been found in the visual system of all invertebrate and vertebrate animals where moving stimuli have been used to interrogate the visual system, and so it seems safe to assume these neural specializations are universal. Moreover, wherever motion-detecting neurons occur, it seems that the underlying mechanism in all species is produced by delayed asymmetric lateral inhibition. Object motion sensitive neurons have been found in flies, bees, locusts, crickets, praying mantises, and dragonflies, and also in fish, salamanders, turtles, frogs, toads, chickens, pigeons, owls, mice, rats, cats, ferrets, wallabies, and several species of monkey. Perhaps the most extensive studies have been conducted on the middle temporal cortical area of the macaque monkey cortex.

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