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W Timberlake

Publications and source records attributed to W Timberlake.

30 records · Page 2Linked to original sources

Time horizons in rats: the effect of operant control of access to future food.

The primary goal of this experiment was to determine whether the addition of an operant requirement for access to a less costly (continuous reinforcement) patch of future food increased the time horizon over which that future patch decreased intake in a currently available depleting (progressive-ratio) patch. Three groups of 4 rats were tested. Each member of the earned-time group was required to cumulate a fixed-time outside the progressive-ratio patch to obtain access to food in the less costly patch; the fixed-time requirement ranged from 2 to 64 min. Rats in the matched-time group received response-independent access to less costly food at the average delay shown by the earned-time group. Rats in the matched-time no-food group were removed from the chamber at the same average delay without receiving access to less costly food. Two of the earned-time rats showed an increased time horizon relative to that shown by the matched-time rats (approaching 40 min for 1 rat). The other 2 earned-time rats markedly increased instrumental responding but showed suppression of intake only when food was less than 20 min away. The matched-time group showed less suppression of intake over a similar range of delay intervals. Surprisingly, the matched-time no-food animals also showed suppression of intake concentrated at the end of the session, possibly reflecting the receipt of their entire daily ration 30 min after the session. The potential importance of time horizons to the foraging process is clear, but experimenters are still working out paradigms for investigation of these horizons.

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On the distinction between open and closed economies.

Open and closed economies have been assumed to produce opposite relations between responding and the programmed density of reward (the amount of reward divided by its cost). Experimental procedures that are treated as open economies typically dissociate responding and total reward by providing supplemental income outside the experimental session; procedures construed as closed economies do not. In an open economy responding is assumed to be directly related to reward density, whereas in a closed economy responding is assumed to be inversely related to reward density. In contrast to this predicted correlation between response-reward relations and type of economy, behavior regulation theory predicts both direct and inverse relations in both open and closed economies. Specifically, responding should be a bitonic function of reward density regardless of the type of economy and is dependent only on the ratio of the schedule terms rather than on their absolute size. These predictions were tested by four experiments in which pigeons' key pecking produced food on fixed-ratio and variable-interval schedules over a range of reward magnitudes and under several open- and closed-economy procedures. The results better supported the behavior regulation view by showing a general bitonic function between key pecking and food density in all conditions. In most cases, the absolute size of the schedule requirement and the magnitude of reward had no effect; equal ratios of these terms produced approximately equal responding.

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Time horizons in rats foraging for food in temporally separated patches.

An important tenet of optimal foraging theory is that foragers compare prey densities in alternative patches to determine an optimal distribution of foraging behavior over time. A critical question is over what time period (time horizon) this integration of information and behavior occurs. Recent research has indicated that rats do not compare food density in a depleting patch with that in a rich patch delayed by an hour or more (Timberlake, 1984). In the present research we attempted to specify over what time period a future rich patch would affect current foraging. The effect of future food was measured by early entry into the rich patch (anticipation) and by a decrease in food obtained in the depleting patch (suppression). The rats showed anticipation of a rich patch up to an hour distant, but suppressed current feeding only if the rich patch was 16 min distant or less. The suppression effect appeared mediated by competition for expression between anticipatory entries into the rich patch and continued foraging in the depleting patch. These results suggest that optimal foraging is based on a variety of specific mechanisms rather than a general optimizing algorithm with a single time horizon.

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System-specific differences in behavior regulation: overrunning and underdrinking in molar nondepriving schedules.

In two experiments we tested the molar regulation prediction that animals adjust schedule performance to reduce deviations from baseline response totals. Both experiments constrained the baseline drink-burst length under molar nondepriving schedules but allowed rats to continue running without drinking. In Experiment 1, rats were required to run in order to drink. In Experiment 2, water was delivered independently of running by fixed-time (FT) schedules. Under the run-to-drink contingency, rats exceeded their baseline amounts of running (overrunning) but failed to maintain their baseline water intake (underdrinking). The total amount of running that did not lead to drinking approximated baseline running. Under the FT schedules, rats again underdrank, but total running approximated baseline. These results do not support previous studies that have shown molar equilibrium effects under nondepriving reciprocal schedules. We conclude that (a) contingent running may not substitute for independent running; (b) intermittent access to water reduces the total instigation for drinking; (c) molar regulation differs under reciprocal and nonreciprocal schedules; and (d) more dynamic, system-specific regulatory models need to be developed.

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Schedule constraint on the average drink burst and the regulation of wheel running and drinking in rats.

Two experiments compared predictions of a molar-pattern model and a general molar behavior regulation model by requiring rats to wheel run for access to water. In both experiments schedule parameters constrained the baseline average burst length of drinking without constraining total drinking. Five levels of schedule constraint were imposed on time spent per drinking burst (Experiment 1) or the number of drinks per burst (Experiment 2). The results of both experiments supported the general molar behavior regulation view but not the molar-pattern model by showing no increase in total wheel running and no decrease in total drinking under schedule constraint. However, both experiments also showed local effects of drink burst constraint, including a direct relation between the degree of constraint and the local rate of drinking, and an approximation of the temporal distribution of baseline drinking under all degrees of schedule constraint. Most local changes support the view that rats defend the baseline temporal distribution of responding under schedule constraint, though some changes appear related to disruption of local response pattern characteristics.

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The basis of superstitious behavior: chance contingency, stimulus substitution, or appetitive behavior?

This research examined three explanations for the "superstitious" behavior of pigeons under frequent fixed-time delivery of food: accidental response-reward contingency, stimulus substitution, and elicited species-typical appetitive behavior. The behavior observed in these studies consisted of occasional postfood locomotion away from the food hopper, and a predominant pattern of activity directed toward the hopper wall (wall-directed behavior), including approaching, stepping side to side, scratching with the feet, bumping with the breast, pendulum movements of the extended neck, and head bobbing, though not pecking. The consistency of these behavior patterns argued against explanation by accidental response contingencies, and the complexity of behavior was incompatible with the classic stimulus-substitution account. These studies also showed that: (1) response contingencies and prior stimulus experience can modify wall-directed behavior, but within definable limits; (2) pecking sometimes can be obtained in birds of specific strains, and by providing extended training; (3) placing the hopper in the floor at the center of a large chamber replaces wall-directed behavior with circling in a manner that resembles ground foraging for food. We conclude that superstitious behavior under periodic delivery of food probably develops from components of species-typical patterns of appetitive behavior related to feeding. These patterns are elicited by a combination of frequent food presentations and the supporting stimuli present in the environment.

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Odor cue determinants of urine marking in male rats (Rattus norvegicus).

This study examined the spatial distribution of urine marking by sexually inexperienced male rats under six odor conditions: minimum odor (baseline), conspecific male urine, conspecific female urine, an animal's own urine, male gerbil urine, and amyl acetate. The gerbil urine and amyl acetate conditions were included to test the theory that marking, rather than being elicited by and directed as a display to appropriate conspecifics, occurred to the introduction of any novel or disruptive odor. The subject's own urine was used to test the theory that the animal marked to maintain an optimum level of its own odor in the environment. The results showed that marking was directed predominantly at objects in the environment over which the animal could readily pass. All odor conditions except "own odor" sharply increased marking over baseline levels. Marking decreased with repeated exposure to particular stimuli. The results strongly supported the theory that urine marking, at least in sexually inexperienced male rats, is produced by novel odor stimuli introduced into a familiar environment.

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Stimulus and response contingencies in the misbehavior of rats.

Misbehavior by rats, in the form of unnecessary and species-typical pawing, nosing, carrying, chewing, and retrieving a rolling ball bearing, was produced by pairing the ball bearing with food (Pavlovian procedure, Experiments 1 and 2) or by requiring contact with the ball bearing for food (operant procedure, Experiments 4 and 5). Misbehavior occurred both before and after eating the food pellet. The frequency, complexity, and duration of pre-pellet misbehavior was increased by delay of food until after the ball bearing exited (or was programmed to exit) and by requiring contact with the bearing to obtain food. Alternative goal-directed behavior, in the form of nosing, gnawing, and licking the food tray, occurred in Pavlovian contingencies in which food was delivered before the bearing was programmed to exit. Post-pellet misbehavior tended to occur when food was delivered before the bearing was programmed to exit and, in the case of required contact, before the animal released the bearing. Omission of food delivery on contact reduced the duration, complexity, and frequency of misbehavior, though experienced animals continued to contact (Experiment 3). In general, misbehavior was affected by both stimulus- and response-reward contingencies but showed characteristic organization and topography under both types of contingency.

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Long T methamphetamine schedules produce circadian ensuing drug activity in rats.

Eight female Sprague-Dawley rats were housed in isolated continuous 24-h/day environments under conditions of constant dim light and a rate-limited feeding schedule. Following 2 months of free-running activity, all animals were administered methamphetamine (MA) i.p. (2 mg/kg) once every 31 h for 24 injection cycles. Average wave forms of wheel-running activity showed that animals did not anticipate the 31-h schedule of MA injections, but rather displayed circadian ensuing drug activity (CEDA) between 24 and 28 h following the injections. Post-injection meals failed to meet reliably the threshold necessary to achieve food-engendered anticipatory or ensuing activity. Cosinor analysis showed that the intensity of CEDA was strongly influenced by the relative phase of the free-running rhythm. CEDA was moderately influenced by the size of the post-injection bout of activity. Because injection times rotated daily throughout local time without repeating a time of day, CEDA resulting from a long T schedule of MA administration appeared to be based on one-trial resetting of a circadian-related mechanism by a major drug of abuse.

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Meal-engendered circadian-ensuing activity in rats.

Large meals scheduled at greater-than-circadian periods (such as T = 31 h) tend to elicit enhanced activity approximately 24 h subsequent to receipt. These studies characterized the process responsible for this meal-engendered "circadian ensuing activity" (meal CEA). Female Sprague-Dawley rats were housed in stations containing a running wheel, pellet dispenser, and lights. Young, middle-aged, or suprachiasmatic-nucleus (SCN)-lesioned rats were given two 1-h meals every 31 or 34 h. Meals were separated by alternating short and long fasts. Most young intact rats engaged in enhanced activity approximately 24 h subsequent to the start of the two-meal series. This circadian ensuing activity underwent large, abrupt daily displacements in response to daily meal delays, was manifested to some degree at all times of day, had an amplitude that was modulated by circadian time of day, was attenuated in middle-aged rats, was evident in SCN-lesioned rats, and oscillated following termination of the feeding schedule. A single experience with food at a novel time of day can "reset" an SCN-independent oscillating process responsible for a circadian activity pattern. CEA has features not readily accommodated by present models of "food-anticipatory activity." The readiness with which the process can be reset implies a keen sensitivity to shifts in the time of food availability but could also produce aberrant behavioral patterns. A T >> 24-h feeding schedule appears to be an ideal procedure with which to study the specific food-related factors responsible for resetting circadian processes and producing a subsequent reallocation of daily activity.

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Facilitation of efficient search of an unbaited radial-arm maze in rats by D1, but not D2, dopamine receptors.

Dopamine (DA) agonists facilitate and antagonists inhibit conditioned preparatory behaviors in rats. We provide added evidence that increased D1 receptor activation facilitates unconditioned preparatory behavior as well, this time in the form of efficient search of an unbaited radial-arm maze. Administration of 0.1, but not 1.0, mg/kg sc SKF81297, a full D1 agonist, increased the number of novel arms chosen in the first eight arms entered. Treatment with 0.1 mg/kg sc D-amphetamine, an indirect DA agonist, also increased search efficiency when given on the first test day but not when given following a test day with a 1.0 mg/kg dose. The 0.1-mg/kg amphetamine-induced facilitation was blocked by coinjection of 0.005 mg/kg SCH23390, a D1 antagonist. Treatment with quinpirole, a D2 agonist, or eticlopride, a D2 antagonist, decreased amount of maze search, but did not affect efficiency. Collectively, our results support the possibility there is a general facilitatory effect of D1 activation on unconditioned preparatory behavior.

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