Perceiving visual expansion without optic flow.

When an observer moves forward in the environment, the image on his or her retina expands. The rate of this expansion conveys information about the observer's speed and the time to collision. Psychophysical and physiological studies have provided abundant evidence that these expansionary motions are processed by specialized mechanisms in mammalian visual systems. It is commonly assumed that the rate of expansion is estimated from the divergence of the optic-flow field (the two-dimensional field of local translational velocities). But this rate might also be estimated from changes in the size (or scale) of image features. To determine whether human vision uses such scale-change information, we have synthesized stochastic texture stimuli in which the scale of image elements increases gradually over time, while the optic-flow pattern is random. Here we show, using these stimuli, that observers can estimate expansion rates from scale-change information alone, and that pure scale changes can produce motion after-effects. These two findings suggest that the visual system contains mechanisms that are explicitly sensitive to changes in scale.

Mechanisms of visual motion detection.

Visual motion is processed by neurons in primary visual cortex that are sensitive to spatial orientation and speed. Many models of local velocity computation are based on a second stage that pools the outputs of first-stage neurons selective for different orientations, but the nature of this pooling remains controversial. In a human psychophysical detection experiment, we found near-perfect summation of image energy when it was distributed uniformly across all orientations, but poor summation when it was concentrated in specific orientation bands. The data are consistent with a model that integrates uniformly over all orientations, even when this strategy is sub-optimal.

Local velocity representation: evidence from motion adaptation.

Adaptation to a moving visual pattern induces shifts in the perceived motion of subsequently viewed moving patterns. Explanations of such effects are typically based on adaptation-induced sensitivity changes in spatio-temporal frequency tuned mechanisms (STFMs). An alternative hypothesis is that adaptation occurs in mechanisms that independently encode direction and speed (DSMs). Yet a third possibility is that adaptation occurs in mechanisms that encode 2D pattern velocity (VMs). We performed a series of psychophysical experiments to examine predictions made by each of the three hypotheses. The results indicate that: (1) adaptation-induced shifts are relatively independent of spatial pattern of both adapting and test stimuli; (2) the shift in perceived direction of motion of a plaid stimulus after adaptation to a grating indicates a shift in the motion of the plaid pattern, and not a shift in the motion of the plaid components; and (3) the 2D pattern of shift in perceived velocity radiates away from the adaptation velocity, and is inseparable in speed and direction of motion. Taken together, these results are most consistent with the VM adaptation hypothesis.

Changes in striatal dopamine metabolism during the development of morphine physical dependence in rats: observations using in vivo microdialysis.

The present study examined the effect of prolonged morphine treatment on striatal dopamine (DA) release and metabolism, during the initial phase of the development of morphine dependence. Sprague-Dawley rats were implanted with chronic guides for microdialysis of the striatum. Morphine (two 75-mg pellets, subcutaneous implant) or placebo was given (12 hr) to pentobarbital anesthetized animals. Following recovery from anesthesia, morphine physical dependence was verified by the naloxone-evoked abstinence syndrome. Morphine produced significant increases in the dialysate level of DA nad its metabolites (DOPAC and HVA) above baseline compared to placebo treatment. HVA levels began to increase immediately following morphine administration, whereas DA and DOPAC levels began to increase after a latency of one and three hr, respectively. Morphine effects on striatal DA metabolism included changes in the metabolic disposition of DA. Increases in HVA concentration accompanied increases in DOPAC concentration up to a threshold value of DOPAC efflux; further increases in DOPAC level were associated with decreases in HVA level. These in vivo data suggest that morphine-induced changes in the regulation of striatal dopaminergic function may be an important component of the development of physical dependence.