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1.
Social memory was investigated in the context of a spatial working memory task. Pairs of rats were tested in an eight-arm
radial maze. Under most conditions, there was a tendency to choose maze locations that had been visited earlier by the other
rat. The possibility that this tendency is produced by common preferences for particular maze locations was ruled out. An
opposite tendency to avoid visits to locations that had been visited earlier during the trial by another rat was found only
when the maze location contained two pellets (rather than an undepletable supply), the rats’ ability to see each other in
the maze was restricted to the central arena, and the maze location had been previously visited by the focal rat. The amount
of food available in maze locations did not otherwise modulate social influences on spatial choice. The results indicate that
memory for a rat’s own previous choices is combined with memory for the choices made by another rat. 相似文献
2.
An attempt was made to disrupt memory for spatial information by interpolating a task of high similarity to the to-be-remembered task during a long retention interval. Rats were trained in an 8-arm maze in which choosing each arm without repetition was the optional strategy. A 4-h delay was imposed between the 4th and 5th choices. At various times during the retention interval, the rats ran a second identical maze located in another room. No evidence of retroactive interference was observed. In the second experiment, the rat was required to remember the interpolated spatial task during the retention test. This was accomplished by allowing the rat to make four choices in the first maze and then, after a variable period of time, four choices in the second maze. Four hours after exposure to each maze, retention was tested. Choice accuracy on the retention tests was high and equivalent on both mazes. Requiring the rat to remember which arms it had visited in a second maze did not impair memory for the first maze. These results demonstrate that rats can segregate spatial memories established in different contexts with considerable proficiency. 相似文献
3.
Treatments that interfere with animals’ short-term retention (e.g., in delayed matching-to-sample) were studied using a spatial memory task. Rats performed in an eight-arm radial maze in which choosing each arm without repetition was the optimal behavior. Performances were interrupted between fourth and fifth choices for a delay of 15 sec to 2 min. A variety of events occurring during the delay interval did not disrupt memories for prior choices (as assessed by the accuracy of postdelay choices). The ineffective treatments included variations in visual and auditory environments, removal from the maze, food consumed during the delay, a distinctive odor added to the maze, or combinations of these manipulations. Additionally, performance on another spatial task (a four-arm maze) during the delay between Choices 4 and 5 did not interfere with performance in the eight-arm maze. These findings suggest that rats’ memories for spatial locations are immune to retroactive interference, at least within the range of conditions reported, and that the rat can successfully segregate memories for spatial locations established in different contexts. 相似文献
4.
William A. Roberts 《Learning & behavior》1981,9(4):566-574
Two experiments were carried out in which rats first were given four forced choices on an eight-arm radial maze, then were given interpolated maze experiences, and finally were given a free choice retention test on the first maze. In Experiment 1, interpolated experiences consisted of forced choices made on one, two, or three other mazes, each placed in a different room. Retroactive inhibition (RI) was not found with one and two interpolated mazes but was found with three interpolated mazes. In Experiments 2a and 2b, an attempt was made to produce RI within a single context by using two mazes placed side by side or on top of one another and by using interpolated forced choices that were different, random, or the same with respect to forced choices onMaze 1. These conditions failed to yield any evidence of RI. In Experiment 2c, forced choices were followed by interpolated direct placements on the same maze on different, random, or the same maze arms, and retention tests revealed RI under these conditions. It was concluded that rats encode memories of specific places visited in space and that RI will arise only if (1) memory is greatly overloaded with interpolated information or (2) an interpolated visit is made to exactly that position in space to which an animal must travel in order to achieve a correct choice on the retention test. 相似文献
5.
Rats were trained in a three-alternative spatial delayed matching-to-sample task in a starburst maze. Samples consisted of rewarded forced choices of one arm, and retention was indicated by rats’ returning to that arm after a 90-sec delay. If a rat made an error on its first choice, it was returned to the start compartment and allowed a second choice. Unlike in previous experiments with this task, all three arms were available during the animals’ second choices. The rats tended to perseverate in their second choices by returning to the arm that they had erroneously visited on their first choice. In Experiment 1, the accuracy of second choices following first-choice errors was below chance during the first block of sessions, when a 90-sec delay intervened between the first choice and the second choice, and at chance during the second block of sessions, when a short (5–6 see) delay intervened between first and second choices. In Experiment 2, long-delay and short-delay sessions were randomly presented to naive subjects. Similar results were obtained. In both experiments, the tendency to repeat the erroneous first choice was greater when long delays separated the two choices than when short delays were used. The results suggest that rats make their first-choice errors because they erroneously encode or remember the location of the sample and that they base their second choices on the same erroneous-memory. The increase in perseveration at long delays implies some kind of rehearsal-like mechanism that slows forgetting of the memory controlling the first choice. 相似文献
6.
Rats (n=4) searched for food on an eight-arm radial maze. Daily 56-min sessions were divided into eight 7-min time zones, during
each of which a different location provided food; locations were randomized across subjects before training. The rats obtained
multiple pellets within each time zone by leaving and returning to the correct location. Evidence that the rats had knowledge
about the temporal and spatial features of the task includes the following. The rats anticipated locations before they became
active and anticipated the end of the currently active locations. The rats discriminated currently active locations from earlier
and forthcoming active locations in the absence of food transition cues. After the rats had left the previously active location,
they visited the next correct location more often than would be expected by chance in the absence of food transition cues.
The rats used handling or opening doors as a cue to visit the first location and timed successive 7-min intervals to get to
subsequent locations. 相似文献
7.
The performance of individual honeybees pretrained to forage at a laboratory window was studied in three rudimentary analogues of the radial maze designed for the study of short-term spatial memory in rats. A linear arrangement of three targets was used in Experiment 1, a triangular arrangement of three targets in Experiment 2, and a rectangular arrangement of four targets in Experiment 3, with reward only for the first response to each of the targets presented on any given trial. Several systematic patterns of responding were observed, with no indication that the choices made by the animals were influenced by memory of targets recently visited. 相似文献
8.
In Experiment 1, rats foraged for food in six successive phases with 8, 16, 24, 32, 40, and 48 arms attached in random locations to a large radial maze. The percentage of novel choices appeared to be determined more by spatial proximity than by number of arms. In Experiment 2, rats foraged for food in four successive phases with 8, 16, 24, and 48 arms attached to the maze in spread-out or tight configurations. Performance was poor in the tight configurations regardless of the number of arms. Performance was excellent in the 8-arm spread-out condition but declined as 16 and, then again, 24 arms were added. Thus, spatial separation, not number of locations, was the chief determinant of performance in the first two experiments. In Experiment 3, in successive phases, 8, 16, 24, 32, 40, 48, 16, and 8 food towers were set in a circle on the floor, with the spatial separation between adjacent towers held constant at 33 cm. The percentage of novel choices declined as 8 towers became 16 and did not change again with 24, 32, 40, or 48 towers in place but then increased again as 16 towers became 8. In Experiment 4, in successive phases, 8, 16, 24, and 32 food towers were set in a circle, with the spatial separation between adjacent towers held constant at 66 cm. The percentage of novel choices declined as 8 towers became 16 and again as 16 towers became 24 but did not decline further. These data were discussed in terms of the fundamental problems posed by variations in the number of food locations in the pursuit of the limit of spatial memory in rats. 相似文献
9.
Rats were given three stages of training on an eight-arm, elevated radial maze with food reward at the end of each arm. In Stage 1, rats were allowed to choose freely among the arms from the beginning of a trial. In Stage 2, three initial forced choices were followed by a series of free choices. In Stage 3, the central platform of the maze was rotated with the rat on it between the initial forced choices and the free choices. Following testing on these three stages, the animals were divided into four groups and deprived of selected senses. One group was made blind, a second anosmic, a third blind and anosmic, and a fourth was left normal. The same three stages of testing that had been conducted preoperatively then were run again post-operatively. Throughout these tests, the possible use of auditory cues was tested by presenting white noise on alternate trials. Finally, two further tests were carried out, the multiple rotations test and the removal-replacement test. The results indicated that visual cues, but not olfactory or auditory cues, played a critical role in the rat’s ability to avoid previously entered alleys. There was evidence also that rats used internal cues from kinesthetic and/or vestibular receptors when visual cues were absent. 相似文献
10.
In two experiments, we examined how the introduction of vertical or horizontal irregularities in the perfectly regular shape of a radial maze affected rats’ performances. The introduction of various tilts in each arm of an eight-arm radial maze had a slightly positive effect on accuracy. However, when intra- and extraraaze cues were dissociated by rotating the maze before maze completion, the rata relied preferentially on extramaze cues associated with the horizontal direction of the arms but not with the tilts. On the other hand, the rats showed poor performances when trained on a horizontally distorted maze (uneven angles between the arms instead of repeated 45° angles). The high number of errors was related to the neglect of particular arms, the disorganization of the patrolling sequences, and the tendency to chain the visit of five arms that formed a regular ahape. Other animals, trained in the same maze, displayed similar biases even after a pretraining phase with constrained choices. Results from the horizontally distorted maze confirm and extend data from the spontaneous alternation literature that choice behavior is influenced by rules of movement that favor large angle transitions and regular subdivisions of space. They also stress the relation between performance in the radial maze and spontaneous exploratory and foraging behaviors. 相似文献
11.
The resource-distribution hypothesis states that the ability of an animal to remember the spatial location of past events is related to the typical distribution of food resources for the species. It appears to predict that Norway rats would perform better than domestic pigeons in tasks requiring spatial event memory. Pigeons, tested in an eight-arm radial maze, exhibited no more than half of the memory capacity observed in rats in the same apparatus and may not have used spatial memory at all. The results were interpreted as supporting the hypothesis. 相似文献
12.
The cognitive mechanisms involved in spatial choice when access to visual cues is restricted were examined in three experiments using male rats. A specially constructed radial-arm maze was used, in which extramaze visual cues could not be perceived from the central arena, but could be perceived from the maze arms. Choices were very accurate when the maze was not rotated during each trial, but inaccurate when the maze was rotated. This suggests that intramaze cues were involved in the control of choices. However, the data clearly showed that choices were not simply controlled by intramaze cues. Rather, control by intramaze cues interacted in a more complex manner with representations of the spatial locations of goals. Such spatial representations were involved in the control of choice despite the absence of visual spatial cues at the time choices were made. 相似文献
13.
Rats were trained on an interval time-place learning (TPL) task in which the location of food availability depended on the
time since the start of the session. Each of four levers (numbered 1, 2, 3, 4) provided food on an intermittent schedule for
two nonconsecutive 3-min periods. The order in which the levers provided food was 1, 2, 4, 3, 2, 3, 1, 4. This order was consistent
across sessions. Previous research conducted in our lab has shown that when only four “places” are used, rather than the eight
in the present study, rats use a timing strategy to track the location of food. Pizzo and Crystal (2004) recently trained
rats on an interval TPL in which each of eight arms of a radial arm maze provided food. They found evidence suggesting that
rats used both spatial and temporal information. In the present study, in which a revisiting strategy was used (i.e., each
lever provided food on more than one occasion), the rats tracked both the spatial and the temporal availability of food for
the first half of the session. Interestingly, in the second half of the sessions, the rats appeared to be timing the availability
of food even though they did not know where it would occur. That is, the rats knew the temporal, but not the spatial, contingencies
for the second half of the session. It appears that the requirement of revisiting a previously reinforced lever resulted in
rats' no longer being able to solve the spatial aspect of the task. 相似文献
14.
Willson and Wilkie (1993) developed a novel procedure for assessing pigeons’ memory for the spatial location of food. Only one of four locations (consisting of an illuminated pecking key and grain feeder) provided food each day. Over days, different locations provided food. The pigeons’ tendency to revisit the location that was profitable on the previous day demonstrated memory for food-spatiallocation associations over a period of 24 h, retention longer than previously reported for this species. This basic finding was replicated and extended in three experiments. Experiment 1 demonstrated that location-food discriminations were also remembered well when established with successive rather than concurrent procedures. Experiment 2 demonstrated that pigeons can remember two location-food associations over 24 h. Experiment 3 showed that the discrimination training inherent in this paradigm is important for retention; retention was impaired when only the rewarded location was presented. Overall, this research suggests that cross-species differences in spatial memory performance may be due to quantitative rather than qualitative differences in the memory system underlying performance. 相似文献
15.
Rats foraged on a four-arm radial maze with one, two, three, and four food items (0.65.g pieces of cheese) placed on different arms (patches) of the maze. In two experiments, the hypothesis was tested that rats should carry food to the center of the maze more often when a patch contains one food item than when it contains multiple food items. Support for this prediction was found when the tendency to carry initial items encountered in patches was compared among the different sized patches. However, a further observation failed to support the hypothesis: Food carrying declined from first to last item encountered in multiple-item patches with clustered food items. Experiment 1 revealed that food carrying was reduced when travel time was increased by barriers placed at arm entrances. Both Experiments 1 and 2 indicated that the tendency for rats to carry food to the center of the radial maze increased as the distance of food encountered on an arm increased from the center. In both experiments, some rats dealt with the problem of multiple items by resorting to multiple-item loading, and some rats carried food items from the end of an arm to a point on the arm nearer the center for consumption. 相似文献
16.
John D. Batson Michael R. Best Deborah L. Phillips Hemlata Patel Kevin R. Gilleland 《Learning & behavior》1986,14(3):241-248
Thirsty rats were trained to collect small water rewards from the end of each arm of an eight-arm radial maze. During these training trials and subsequent testing trials, the subjects were allowed to choose a maximum of eight arms. “Preference” for a target maze location was studied by noting when, in the sequence of eight choices, the target was selected. During testing, when one maze location was consistently devoid of water, rats decreased their preference for this arm over trials (Experiment 1). Similarly, rats that learned a saccharin-lithium association demonstrated lower preferences for a maze location that consistently held the conditioned saccharin solution. This was true for animals that received saccharin-lithium conditioning on the maze (Experiment 3A) and for animals conditioned to saccharin in a separate context (Experiment 3B). An increase in preference for a target maze location consistently containing a sweet chocolate milk solution was observed in animals that were water- and food-deprived (Experiment 2). These studies demonstrate that animals will modify their responses toward (preferences for) maze locations that predictably contain an altered reward. 相似文献
17.
Rats were trained to forage for food on a four-arm radial maze. Each arm of the maze was defined as a patch and contained four feeding stations. Each patch contained a total of 20 45-mg food pellets, with the first feeding station in each patch baited with 1 pellet and the remaining stations baited with 1, 5, or 13 pellets. In Experiment 1, one group of rats was tested with feeders open and food readily accessible, and another group was tested with metal covers on the feeders, which necessitated extra time to gain access to food. With open feeders, the rats visited each feeder in a patch in the order in which they encountered the feeders, from the center of the maze to the end of the arm. The rats in the group with the covered feeders often visited the feeders containing 5 or 13 pellets first and the feeders containing 1 pellet last. In Experiment 2, it was found that the rats switched readily between these two foraging strategies when tested with covered and open feeders on alternate sessions. The extra time and effort required to uncover food appeared to produce selective foraging in rats. 相似文献
18.
David C. Zuckerman 《Learning & behavior》1975,3(3):250-256
Four rats were each trained to perform a light-intensity discrimination and a sound-intensity discrimination. For half of the subjects, light training sessions were preceded by food deprivation, and correct choices were reinforced with food. Sound training sessions, on the other hand, were preceded by water deprivation, and correct choices were reinforced with water. For the remaining subjects, light training sessions were associated with water deprivation, whereas sound sessions were associated with food deprivation. When the rats were tested in the presence of compounds of sound and light, choices tended to be controlled by light when testing was preceded by the deprivation condition associated with light discrimination task. Reliably fewer light-consistent choices were made under the other deprivation condition, though some preference for responding on the basis of light remained. Following extended training in the presence of all four combinations of light and sound stimuli, this preference was reduced somewhat. When additional testing sessions were preceded by combined food and water deprivation, the tendency to respond on the basis of either light or sound was shown to be related to both deprivation and reinforcement factors. 相似文献
19.
The conditions necessary for producing retroactive interference (RI) were examined in a 12-arm radial maze. Rats were first given either three or nine forced choices in a to-be-remembered maze. During a 2-h delay, they received one or two trials in a second 12-arm maze, located either in a different room or the same room as the to-be-remembered maze. During the postdelay memory test, RI from the interference trials was produced only when nine choices had been made in the to-be-remembered maze and two interference trials had been conducted during the delay interval. RI was not found when only three forced choices had to be retained or after a single interference trial. The similarity between the interpolated and to-be-remembered mazes had no effect on choice accuracy. It was concluded that two conditions are required for the production of RI in the radial maze. First, a “large amount” of information should be resident in working memory. Second, a substantial number of interpolated trials or choices must be made during the delay. 相似文献
20.
Cynthia M. Hoffman William Timberlake Joseph Leffel Rory Gont 《Learning & behavior》1999,27(4):426-444
Norway rats have been shown to depend on short-term spatial memory to find food on a radial arm maze (RAM), but what locomotor search tactics are involved in using this memory effectively? Four experiments distinguished tactics of distance minimizing, central-place search, trail following, thigmotactic search, and random search by using different configurations of a RAM placed flat on the floor of an arena. These search tactics make similar predictions on an elevated RAM but predict different outcomes on a floor RAM because the rats are free to approach the food from any direction. After initial trials dominated by exploration, rats traveled along arms to food, even when the resultant distance was up to three times the minimum distance. With no food present, rats also traveled along arms; with no arms up to present, they traveled along walls to food. It appears that both maze arms and arena walls engage mechanisms related to trail following in rats. 相似文献