A New Maze Technique

E. D. Adrian. The Mechanism of Nervous Action. Philadelphia: Univ. Pa. Press, 1932. Pp. x+103. Reviewed by Clarence H. Graham.     

Sex of Experimenter and Intelligence as Factors in Maze Learning: A Further Comparison of Maze and Sex Differences

(Murphy, Lois Barclay. Social Behavior and Child Personality. New York: Columbia Univ. Press, 1937. Pp. 333.)     

Time Records in Human Maze Learning and their Comparison with Maze Records

Nine measures of role-taking in the tradition of Flavell and two measures of classification were administered to 64 boys and girls in India in four age groups: 6–7, 7–8, 8–9, and 9–10 years. The results lend cross-cultural support to the hypothesis that certain classification skills underlie this type of role-taking ability. The inappropriateness of searching for developmental relationships with some parametric statistics was also demonstrated with these data. The influence of two types of role-taking question on role-taking ability was also assessed. Role-taking questions were asked after the Ss had seen a cartoon sequence. On one type of role-taking question (a “next” question) Ss were asked how another child would think the cartoon ended if shown only the beginning. On the other type of role-taking question (a “before” question) Ss were asked how another child would think the cartoon began when shown only the end. Cartoon content was shown to influence role-taking ability in response to “next” questions.     

Maze Learning by Honeybees

This study examines whether honeybees can learn to fly through complex mazes, in the presence or the absence of specific visual cues. The results are summarized as follows: 1. Bees can learn to fly through a complex maze by following a trail of colored marks. 2. Bees, initially trained to follow color marks through an initial part of the maze, are immediately able to use the same sign-tracking cue to find their way through the rest of the maze, which is unfamiliar to them. 3. Bees trained to follow color marks through a particular maze can use the same cue to negotiate a novel maze. 4. Bees trained to use a particular color to negotiate a maze can immediately use a novel color to negotiate the same maze or even a novel maze. 5. After learning to negotiate a maze by following colored marks, bees can find their way through the maze even when the marks are removed, albeit at reduced levels of accuracy. Thus, the trained bees do not rely solely on sign-tracking to find their way through the maze: they also acquire a spatial memory of the maze or at least a sequence of motor commands describing the correct path through it. 6. Bees can learn to use color as a signal even when it indicates the path through the maze in a symbolic way, for example, blue indicating a turn to the right and green a turn to the left. 7. Bees can learn an unmarked maze. Performance under these conditions is poorer than when marks are provided, but is still significantly better than chance level. 8. Control experiments rule out the use of external landmarks in all of these situations.     

Maze learning in Alzheimer's disease

Alzheimer's disease (AD) patients and normal elderly controls performed a block of 10 trials on a finger maze, followed by a 45-min period during which verbal learning measures were administered. Subjects then performed an additional 10 trials on the original maze, followed by 10 trials on a new maze. The AD patients and a subset of control subjects decreased mean completion time across Blocks 1 and 2, suggesting skill acquisition. Mean time on Block 3 was significantly less than mean time on Block 1, suggesting skill generalization. A subset of controls did not show the above pattern. The results of this study suggest that AD patients are able to acquire and generalize a cognitively mediated perceptual-motor skill.