Pigeons exhibit higher accuracy for chosen memory tests than for forced memory tests in duration matching-to-sample

Following training to match 2- and 8-sec durations of feederlight to red and green comparisons with a 0-sec baseline delay, pigeons were allowed to choose to take a memory test or to escape the memory test. The effects of sample omission, increases in retention interval, and variation in trial spacing on selection of the escape option and accuracy were studied. During initial testing, escaping the test did not increase as the task became more difficult, and there was no difference in accuracy between chosen and forced memory tests. However, with extended training, accuracy for chosen tests was significantly greater than for forced tests. In addition, two pigeons exhibited higher accuracy on chosen tests than on forced tests at the short retention interval and greater escape rates at the long retention interval. These results have not been obtained in previous studies with pigeons when the choice to take the test or to escape the test is given before test stimuli are presented. It appears that task-specific methodological factors may determine whether a particular species will exhibit the two behavioral effects that were initially proposed as potentially indicative of metacognition.     

Distance distortions in memory for spatial locations

The present study examined developmental differences in the effect of route extensity on the memory for the locations of objects in a spatial array. Kindergarten and adult subjects were trained to remember the locations of 4 objects. During this training, objects were either connected by a combination of indirect, looped train tracks and direct train tracks (experimental subjects) or connected by entirely direct train-track routes (control subjects). Analyses of actual interobject distances, from subjects' reproductions of object locations on a response board (without train tracks), revealed that children, but not adults, distort distance in terms of the nature of travel observed between objects. Further testing revealed that differences in the amount of time taken for travel could not account for the results obtained with children.     

Short-term spatial memory in honeybees

Foraging honeybees were trained individually in two-choice spatial problems. Differentially rewarded for spatial alternation in Experiment 1 (“win-shift” training), they showed instead a clear tendency to perseverate—that is, to prefer on each trial the location of reward on the immediately preceding trial. On the basis of the results of Experiments 2 and 3, in which one location was rewarded over shorter or longer series of consecutive trials, an associative interpretation of the perseveration found in the first experiment was rejected in favor of an interpretation in terms of short-term spatial memory. Experiment 4, in which the animals were rewarded on each trial for choosing either location, also showed perseveration. Honeybees, like rats, seem to remember a rewarded location recently visited, but tend to return to it rather than, like rats, to avoid it.     

Search behavior in cats and dogs: Interspecific differences in working memory and spatial cognition

Cats’ and dogs’ search behavior was compared in different problems where an object was visibly moved behind a screen that was then visibly moved to a new position. In Experiments 1 (cats) and 2 (dogs), one group was tested with identical screens and the other group was tested with dissimilar screens. Results showed that in both species, search behavior was based on processing of spatial information rather than on recognition of the visual features of the target screen. Cats and dogs were unable to find the object by inferring its invisible movement. They reached a high level of success only if there was direct perceptual evidence that the object could not be at its initial position. When the position change was indicated by an indirect cue, cats searched more at the object’s initial than final position, whereas dogs searched equally at both positions. Interspecific similarities and differences are interpreted in terms of the requirements for resetting working memory.     

Retroactive inhibition in rat spatial memory

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.     

Individual differences in spatial text processing: High spatial ability can compensate for spatial working memory interference

The present study investigates the relation between spatial ability and visuo-spatial and verbal working memory in spatial text processing. In two experiments, participants listened to a spatial text (Experiments 1 and 2) and a non-spatial text (Experiment 1), at the same time performing a spatial or a verbal concurrent task, or no secondary task. To understand how individuals who differ in spatial ability process spatial text during dual task performance, spatial individual differences were analyzed. The tasks administered were the Vandenberg and Kuse [Vandenberg, S. G., & Kuse, A. R. (1978). Mental rotation, a group test of three-dimensional spatial visualization. Perceptual and Motor Skills, 47, 599-604.] mental rotation test (MRT) and a reading comprehension task (RCT). Individuals with high (HMR) and low (LMR) mental rotation differed in MRT scores but had similar RCT performance. Results showed that the HMR group, in contrast with LMR counterparts, preserved good spatial text recall even when a spatial concurrent task was performed; however, Experiment 2 revealed a modification of spatial concurrent task performance in LMR as well in HMR group. Overall, results suggest that HMR individuals have more spatial resources than LMR individuals, allowing them to compensate for spatial working memory interference, but only to a limited extent, given that the processing of spatial information is still mediated by VSWM.     

数据存贮新技术综述

数据存贮技术是实现网络宽带通信的关键技术.文章集中介绍了两种数据存贮技术：光存贮技术和网络存贮技术.光存贮技术是硬件存贮技术的发展方向;网络存贮技术是解决光速极限的最有力手段.此外文章对这些技术的应用进行了较深入的分析,并指明了这些技术未来的发展方向.     

MANET在空间复用随机模型下的平均洪泛距离研究

The flooding distance is an important parameter in the design and evaluation of a routing protocol,which is related not only to the delay time in the route discovery,but also to the stability and reliability of the route.In this paper, the average flooding distance (AFD) for a mobile ad hoc network (MANET) in a random graph model was given based on the dynamic source routing (DSR) protocol.The influence of spatial reuse on the AFD was also studied.Compared with that in the model without the spatial reuse,the AFD in the model with the spatial reuse has much smaller value,when the connetivity probability between nodes in the network is small and when the number of reused times is large.This means that the route discovery with the spatial reuse is much more effective.     

The sensory basis of spatial memory in the rat

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.     

Developmental trends for object and spatial working memory: a psychophysiological analysis

This study examined developmental trends in object and spatial working memory (WM) using heart rate (HR) to provide an index of covert cognitive processes. Participants in 4 age groups (6-7, 9-10, 11-12, 18-26, n=20 each) performed object and spatial WM tasks, in which each trial was followed by feedback. Spatial WM task performance reached adult levels before object WM task performance. The differential developmental trends for object and spatial WM found in this study are taken to suggest that these WM components are separable. Negative performance feedback elicited HR slowing that was more pronounced for adults than for children. The development of performance monitoring as indexed by covert HR slowing following performance feedback contributes to WM performance.     

New design of sense amplifier for EEPROM memory

We present a new sense amplifier circuit for EEPROM memory. The topology of the sense amplifier uses a voltage sensing method, having low cost and low power consumption as well as high reliability. The sense amplifier was implemented in an EEPROM realized with an SMIC 0.35-μm 2P3M CMOS embedded EEPROM process. Under the condition that the power supply is 3.3 V, simulation results showed that the charge time is 35 ns in the proposed sense amplifier, and that the maximum average current consumption during the read period is 40 μA. The novel topology allows the circuit to function with power supplies as low as 1.4 V. The sense amplifier has been implemented in 2-kb EEPROM memory for RFID tag IC applications, and has a silicon area of only 240 μm^2.     

Infant imitation and memory: nine-month-olds in immediate and deferred tests

The ability of 9-month-old infants to imitate simple actions with novel objects was investigated. Both immediate and deferred imitation were tested, the latter by interposing a 24-hour delay between the stimulus-presentation and response periods. The results provide evidence for both immediate and deferred imitation; moreover, imitative responding was not significantly dampened by the 24-hour delay. The findings demonstrate that there exists some underlying capacity for deferring imitation of certain acts well under 1 year of age, and thus that this ability does not develop in a stagelike step function at about 18-24 months as commonly predicted. These findings also show that imitation in early infancy can span wide enough delays to be of potential service in social development; actions on novel objects that are observed one day can be stored by the child and repeated the next day. The study of deferred imitation provides a largely untapped method for investigating the nature and development of recall memory in the preverbal child.     

Modality of language shapes working memory: evidence from digit span and spatial span in ASL signers

Deaf children who are native users of American Sign Language (ASL) and hearing children who are native English speakers performed three working memory tasks. Results indicate that language modality shapes the architecture of working memory. Digit span with forward and backward report, performed by each group in their native language, suggests that the language rehearsal mechanisms for spoken language and for sign language differ in their processing constraints. Unlike hearing children, deaf children who are native signers of ASL were as good at backward recall of digits as at forward recall, suggesting that serial order information for ASL is stored in a form that does not have a preferred directionality. Data from a group of deaf children who were not native signers of ASL rule out explanations in terms of a floor effect or a nonlinguistic visual strategy. Further, deaf children who were native signers outperformed hearing children on a nonlinguistic spatial memory task, suggesting that language expertise in a particular modality exerts an influence on nonlinguistic working memory within that modality. Thus, language modality has consequences for the structure of working memory, both within and outside the linguistic domain.     

The effect of active versus passive exploration on memory for spatial location in children.

The effect of active exploration upon memory for spatial location of an event was assessed for children at 2 age levels. Each child took a walk through the same unfamiliar hallway in search of a hidden object which he was later asked to relocate. Half the children were accompanied by an adult holding their hand (passive condition), while the other half proceeded on their own with an adult following behind (active condition). An age x condition interaction revealed that active exploration significantly improved performance of the 3- and 4-year-old group while not affecting the performance of the 9- and 10-year-olds. The 3- and 4-year-olds in the active condition, however, were still significantly less accurate than the older children, despite their experience of self-directed exploration. The results are interpreted as supporting the hypothesis that self-directed activity serves to increase attention of preoperational children to relevant topological cues in the environment, whereas concrete operational children, due to their knowledge of projective and Euclidean space, demonstrate increased capacity to efficiently encode spatial information regardless of the mode of exploration.     

Characteristics of pigeons’ spatial working memory in an open-field task

Although pigeons seem to require special training before they will display accurate spatial working memory in radial-arm mazes, they readily show accurate working memory for recently visited feeder locations in an open-field analog of the radial maze. In this task, pigeons forage among sites located on the floor of an open room, with no constraints on the path they take between sites. Experiment 1 suggested that pigeons’ working memory for recently visited sites is facilitated if they are permitted to develop a stable reference memory “map” of the location of the sites with respect to landmarks in the room: Pigeons for which the landmarks remained constant from day to day displayed more accurate working memory than did pigeons for which the landmarks were rearranged between daily trials. The second experiment investigated the durability of pigeons’ working memory, using a forced-choice procedure. Accuracy remained high for retention intervals of up to 32 min, but dropped significantly with a 2-h delay.     

The existence and extent of spatial working memory ability in honeybees

Honeybees foraged from six locations, each of which was baited with sugar solution prior to each experimental trial. Under a variety of conditions, bees exhibited a small but reliable tendency to avoid revisits to locations that they had visited earlier during the experimental trial. These results replicate those of Brown and Demas (1994), who concluded that bees use working memory to discriminate previously visited locations from those not yet visited. The present experiments included procedures that allowed alternatives to this explanation to be more completely ruled out. The extent of spatial working memory performance exhibited by honeybees in these experiments appears to be limited by a process other than working memory capacity, perhaps the ability of bees to discriminate among several locations in close proximity to one another.     

Further studies of pigeons’ spatial working memory in the open-field task

In Experiments 1 and 2, pigeons’ spatial working memory in an open-field setting was examined under conditions that differed in terms of working-memory load (number of sites visited prior to a retention test) at various delays between initial choices and the retention test. In Experiment 1, pigeons were tested under two conditions of memory load (three or five sites visited prior to the delay) and two delay intervals (15 and 60 min). Accuracy declined as a function of delay but was not affected significantly by memory load. In Experiment 2A, pigeons were tested under three conditions of memory load (two, four, or six sites visited prior to the delay). In separate phases, the delay was 2, 15, and 60 min. Accuracy was not affected by memory load in any of these phases. In Experiment 2B, three conditions of memory load (two, four, or six sites visited prior to the delay) were tested at two delays (2 and 60 min) within a test phase. Accuracy declined with increasing delay, but memory load again had no significant effects. These results are inconsistent with previous suggestions that pigeons’ retention of spatial information may decline as working-memory load is increased. In Experiment 3, cue-manipulation tests confirmed that pigeons’ choice behavior in the open-field task is controlled by memory for previously visitad room locations.