Animal models of source memory

Source memory is the aspect of episodic memory that encodes the origin (i.e., source) of information acquired in the past. Episodic memory (i.e., our memories for unique personal past events) typically involves source memory because those memories focus on the origin of previous events. Source memory is at work when, for example, someone tells a favorite joke to a person while avoiding retelling the joke to the friend who originally shared the joke. Importantly, source memory permits differentiation of one episodic memory from another because source memory includes features that were present when the different memories were formed. This article reviews recent efforts to develop an animal model of source memory using rats. Experiments are reviewed which suggest that source memory is dissociated from other forms of memory. The review highlights strengths and weaknesses of a number of animal models of episodic memory. Animal models of source memory may be used to probe the biological bases of memory. Moreover, these models can be combined with genetic models of Alzheimer's disease to evaluate pharmacotherapies that ultimately have the potential to improve memory.     

任务呈现方式、双任务反应顺序影响算术估算策略选择与执行

采用选择/无选范式,通过操纵任务呈现方式(估算题目的数字消失与否)与主次任务反应顺序(先反应算术任务或先反应字母任务),考察了双任务协调在算术策略选择与执行中的潜在作用。结果显示:(1)不同双任务呈现情境中个体的算术策略表现有明显区别。算术题目数字不消失相比消失时,个体对主、次任务的回答正确率都比较低,在策略选择上更倾向于选择较简单策略,在策略执行上准确性偏低;(2)双任务反应顺序会影响算术策略运用表现。先反应算术任务时,双任务情境只影响策略执行的准确性;而先反应字母任务时,双任务情境对策略执行的准确性和反应速度均发挥干扰作用,且估算题目的数字消失与否对策略选择准确性的影响更大,策略选择适应性之间的差异亦更加明显。上述发现对于深入理解双任务协调功能在策略运用中的作用机制具有重要意义。     

Error is proportional to distance measured by honeybees: Weber’s law in the odometer

Honeybees were trained to fly a specific distance, the same over trials, down a tunnel for a reward. After training, they were tested occasionally with the reward absent. On tests, bees fly to or just past the expected place of reward, then turn around and fly back. After some distance, they turn back again, and may continue turning back and forth a number of times. Past research has shown that distance estimation in this task is based on the retinal flow of visual texture on the walls of the tunnel. Here we measured the errors in distance estimation as a function of training distance. Errors were measured as the standard deviation across trials of the positions of the first two turns (Turn1 and Turn2), and of the Middle (average of Turn1 and Turn2) and Spread (difference between Turn1 and Turn2). All errors were proportional to the training distance, thus obeying Weber’s law. Models of possible mechanisms underlying this phenomenon are discussed. The mean Spread matches the errors in Turn1 and Middle, suggesting that the bee chooses the spread of its search to match the expected odometric error. Received: 28 April 1998 / Accepted after revision: 19 November 1998     

Taking a closer look: time sampling and measurement error

A person manufactured his in-seat behavior for 15, 30-min sessions so that there were three blocks of five sessions where the behavior occurred 20%, 50%, and 80% of the time. Whole interval, partial interval, and momentary time-sample measures of the behavior were taken and compared to the continuous measure of the behavior i.e., per cent of time the behavior occurred. For interval time sampling, the difference between the continuous and sample measures i.e., measurement error, was: (1) extensive, (2) unidirectional, (3) a function of the time per response, and (4) inconsistent across changes in the continuous measure. A procedural analysis demonstrated that the frequency and duration of behavior are confounded in interval time sampling. Momentary time sampling was found to be superior to interval time sampling in estimating the duration a behavior occurs.     

Behavior of humans in variable-interval schedules of reinforcement

During Phase I, human subjects pressed a button for monetary reinforcement in five variable-interval schedules, each of which specified a different frequency of reinforcement. The rate of responding was an increasing, negatively accelerated function of reinforcement frequency; the data conformed closely to Herrnstein's equation. During Phase II, the same five schedules were in operation, but in addition a concurrent variable-interval schedule (B) was introduced, responses on which were always reinforced at the same frequency. Response rate in component A increased while the response rate in B decreased, as a function of the reinforcement frequency in component A. Relative response rates in the two component schedules matched the relative frequencies of reinforcement. Comparing the absolute response rates in component A during Phase I and Phase II it was found that introduction of the concurrent schedule did not affect the value of the theoretical maximum response rate, but did increase the value of the reinforcement frequency needed to obtain any particular submaximal response rate.     

Punishment of responding under schedules of stimulus-shock termination: effects of d-amphetamine and pentobarbital.

Responding maintained in squirrel monkeys under 5-min fixes-interval schedules of either food presentation or termination of a visual stimulus associated with electric-shock delivery was suppressed by presenting an electric shock for every thirtieth response (punishment). In monkeys responding under the schedule of food presentation, d-amphetamine sulfate only further decreased punished responding, and pentobarbital sodium markedly increased punished responding, as expected from previous reports. In monkeys responding under the schedule of stimulus-shock termination, however, the effects of the two drugs were opposite: d-amphetamine markedly increased punished responding, whereas pentobarbital only decreased responding. Thus, the effects of these drugs on punished responding were different depending on the type of event maintaining responding. These and previous results indicate that it may be misleading and inaccurate to speak of the effects of drugs on "punished responding" as though punishment were a unitary phenomenon. As with any behavior, the effects of drugs and other interventions on punished responding cannot be accurately characterized independently of the precise conditions under which the behavior occurs.     

Temporal patterns of responding in small fixed-ratio schedules

Pigeons were exposed to an ascending series of small fixed-ratio schedules from fixed-ratio 1 to 7. Two of those pigeons were later placed on a fixed-ratio 30 schedule. The two primary dependent variables were the postreinforcement pause and the interresponse time. Changes in these variables under small fixed ratios were sometimes opposite to changes reported with large fixed ratios. For example, postreinforcement pauses decreased in length as the fixed-ratio requirement increased from fixed-ratio 1 to fixed-ratio 3. Also, the interresponse times early in the small fixed-ratio schedule were shorter than those immediately preceding reinforcement. These findings question the role of interresponse-time reinforcement in determining temporal patterns of responding under small fixed-ratio schedules. They also suggest that there may be a limited region in which the independent variable, fixed-ratio size, does not operate as previously described.     

The role of verbal behavior in human learning: II. Developmental differences

When children in four different age ranges operated a response device, reinforcers were presented according to fixed-interval schedules ranging in value from 10 to 70 seconds. Only the behavior of the subjects in the youngest of the four groups, the preverbal infants, resembled that of other animal species. The children in age ranges 5 to 6½ and 7½ to 9 years exhibited either the low-rate or high-rate response patterns typical of human adults. Those who showed the low-rate pattern reported a time-based formulation of the contingencies and some of them were observed to occasionally count out the interval before responding. The performance of children aged 2½ to 4 years differed from that of both infants and older children, though containing some patterning elements similar to those produced by the older and younger subjects. The predominant response pattern of the infants consisted of a pause after reinforcement followed by an accelerated rate of responding that terminated when the next reinforcer was delivered. Analysis of postreinforcement-pause duration and response rate showed that infant performance, but not that of the older children, consistently exhibited the same kinds of schedule sensitivity observed in animal behavior. The evidence supports the suggestion that the development of verbal behavior greatly alters human operant performance and may account for many of the differences found between human and animal learning.     

Positive and negative contrast as a function of component duration for key pecking and treadle pressing

Pigeons responded on several multiple schedules for food reinforcers. The duration of the components varied from four seconds to 16 minutes. The absolute size of positive (Experiment 1) and negative (Experiment 2) behavioral contrast varied inversely with component duration when key pecks produced the reinforcers. The absolute size of negative contrast varied directly with component duration, when treadle presses produced the reinforcers (Experiment 3). These results conform to theories that suggest that positive and negative contrast are symmetrical when pigeons peck keys. They also conform to theories that suggest that the same principles do not govern contrast when pigeons peck keys as when they press treadles. Finally, the results support the measurement of behavioral contrast by the differences between baseline rates of responding and the rates emitted when contrast is present.