Three experiments assessed the ability of male Sprague-Dawley rats to organize the spatial locations of different food types in a hierarchical manner to maximize the efficiency of working memory. Independent groups were exposed, on a 12-arm radial maze, to baiting arrangements varying in the stability of the pattern and type of food used as bait. Training rats with stable, differentiable baiting arrangements produced increased accuracy in choice performance, hierarchically ordered patterns of choice selection, slower growth of proactive interference when trials were massed, and the learning of the geometrical relations among food types independent of other extramaze cues. Such findings are strong evidence of the rat's ability to encode and use local cues for navigation, based on properties of the reinforcer. The application of a chunking strategy may provide for more efficient use of working memory by facilitating information storage, recall, or resetting mechanisms.

Localization within the space in front of an observer can be specified along two orthogonal physical dimensions: elevation ('up', 'down') and horizontal ('left','right'). For the erect observer, these correspond to egocentric dimensions along the long and short axes of the body, respectively. However, when subjects are rolled-to-horizontal (lying on their sides), the correspondence between the physical and egocentric dimensions is reversed. Employing egocentric coordinates, localization can be referred to a central perceptual point-visually perceived eye level (VPEL) along the long axis of the body, and visually perceived straight ahead (VPSA) along the short axis of the body. In the present experiment, measurements of VPEL and of VPSA were made on each of eight subjects who were either erect or rolled-to-horizontal while monocularly viewing a long 2-line stimulus (two parallel, 64 degrees -long lines separated by 50 degrees ) in otherwise complete darkness that was centered on the eye of the observer and was tilted out of the frontoparallel plane by a variable amount and direction (from -30 degrees to +30 degrees in 10 degrees steps). The stimulus tilt was either around an axis through the center of the two eyes (pitch; VPEL was measured) or around the long axis of the body that passed through the center of the viewing eye (yaw; VPSA was measured). Large variations in the localization settings were measured that were systematic with stimulus tilt. The slopes of the functions plouing the deviations from veridicality against the orientation of the 2-line stimulus ('induction functions') were larger for the rolled-to-horizontal observer than for the erect observer for both VPEL and VPSA, and for a given body orientation were larger for the VPEL discrimination than for the VPSA discrimination; the influences of body orientation in physical space and the direction of the discrimination relative to the body were lineraly additive. Both the y-intercepts of the induction functions and the central perceptual point measured in complete darkness were lower when the norm setting by the subject was along the vertical than when it was along the horizontal; this held for both the VPEL and VPSA discriminations. The systematic effects of body orientation on the slopes and of line orientation on the y-intercepts and dark values result from an effect of gravity on the settings and fit well to a general principle: any departure from erect posture increases the induction effects of the visual stimulus. The effect of gravity is consistent with the effect of gravity in previous work in high-g environments with the VPEL discrimination.

Bilateral intratympanic sodium arsenate injections (100 mg/ml in isotonic saline) in adult male Long Evans rats produced impairments in allocentric navigation using a 12-arm radial maze procedure as well as a motor test battery designed to evaluate vestibular function. In contrast, no impairments in the accuracy or precision of duration reproduction using 20-s and 80-s peak-interval procedures were observed when both target durations were associated with the same lever response, but distinguished by signal modality (e.g., light or sound). In contrast, an ordinal-reproduction procedure with 800, 3200, and 12,800 ms standards requiring the timing of self-initiated movements during the production phase revealed large impairments in the accuracy and precision of timing for vestibular lesioned rats. These impairments were greater on trials in which self-initiated body movements (e.g., holding down the response lever for a fixed duration) were required without the support of external stimuli signaling the onset and offset of the reproduced duration in contrast to trials in which such external support was provided. The conclusion is that space and time are separable entities and not simply the product of a generalized system, but they can be integrated into a common metric using gravity and self-initiated movement as a reference.

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