Latency of different verbal responses to the same stimulus

A response of reading (letter O) or of naming (circle) can be given to the same sign O. The verbal reaction time is higher when naming than when reading (difference 100 millisec.). This fact verifies that naming is a longer process than reading, the difficulty of perceiving the stimulus being equal.

The response “zero” which may be given to the same sign is nearer to the reading-response time than the naming-response. These facts can be explained if we say that uncertainty for coding concrete signs is greater than for alphabetical or numerical signs.     

Death feigning by grass snakes (Natrix natrix) in response to handling by human "predators."

Death feigning, a variant of tonic immobility, is usually interpreted as a last-resort antipredator measure. The authors describe death feigning in grass snakes (Natrix natrix) and test some of its potential correlates. Death feigning was seen in 66% of wild-caught snakes but was not seen in hatchlings from laboratory-incubated eggs. Minimal indication of death feigning was mouth gaping, often with the tongue hanging free, but more dramatic cases involved voluntary supination and/or lack of muscle tone. Aside from hatchlings, which did not feign death, there was little variation in frequency or intensity of death feigning with body size. There was no effect of body temperature on death feigning nor were snakes that were moving when caught less likely to feign death than those that were not moving. Interpretation of the adaptive value of death feigning in grass snakes or in other animals is hampered by lack of evidence of this behavior in the field in response to natural predators.     

Instantiated features and the use of "rules."

Classification "rules" in expert and everyday discourse are usually deficient by formal standards, lacking explicit decision procedures and precise terms. The authors argue that a central function of such weak rules is to focus on perceptual learning rather than to provide definitions. In 5 experiments, transfer following learning of family resemblance categories was influenced more by familiar-appearing features than by novel-appearing features equally acceptable under the rule. This occurred both when rules were induced and when rules were given at the beginning of instruction. To model this and other phenomena in categorization, features must be represented on 2 levels: informational and instantiated. These 2 feature levels are crucial to provide broad generalization while reflecting the known peculiarities of a complex world.     

"Perhaps it would be better not to know everything."

The advent of statistical methods for evaluating the data of individual-subject designs invites a comparison of the usual research tactics of the group-design paradigm and the individual-subject-design paradigm. That comparison can hinge on the concept of assigning probabilities of Type 1 and Type 2 errors. Individual-subject designs are usually interpreted with implicit, very low probabilities of Type 1 errors, and correspondingly high probabilities of Type 1 errors, and correspondingly high probabilities of Type 2 errors. Group designs are usually interpreted with explicit, moderately low probabilities of Type 1 errors, and therefore with not such high probabilities of Type 2 errors as in the other paradigm. This difference may seem to be a minor one, considered in terms of centiles on a probability scale. However, when it is interpreted in terms of the substantive kinds of results likely to be produced by each paradigm, it appears that the individual-subject-design paradigm is more likely to contribute to the development of a technology of behavior, and it is suggested that this orientation should not be abandoned.     

The effect of discrimination training on responses to a new stimulus

Most previous research on the effect of the duration of preceding discrimination training on responding to a new stimulus has measured the responding during extinction. To reduce effects originating in the extinction procedure itself, the present study assessed the effect of discrimination training on responses to a new negative stimulus added during continued discrimination training. Pigeons were given a new negative stimulus (blue key) after 0, 1, 3, or 9 days of discrimination training with a yellow key as the positive stimulus, and both a green key and a red key as negative. Fewer responses were made to the blue key when it was introduced after nine days of discrimination training than after less discrimination training. That effect of long discrimination training agrees with reported results from extinction tests. However, the effect of briefer discrimination training in the present study differed from reported results with extinction testing. It appears that testing during continued discrimination training eliminates a distortion present in extinction tests of the effect of discrimination training on responding to a new stimulus.     

The effects of environmental change on chicks' responses to a familiar stimulus

The purpose of the present experiments was to explore chicks' proximity seeking behaviour in relation to imprinting objects in unfamiliar settings. Experiment I showed that chicks, which were individually imprinted on a stationary imprinting object, displayed reduced proximity seeking behaviour when tested in a pen smaller than the rearing pen. This finding confirmed earlier work on the effects of changed pen size. Experiment II used continuous and intermittent noise rearing and testing conditions, in all possible combinations, and a stationary imprinting object. Increased proximity seeking was found in conditions where the auditory environment was changed from rearing to testing, a result apparently opposite to that obtained in earlier work. It is suggested that the effect of environmental change on proximity seeking may vary with the modality in which change occurs and the salience of the imprinting object.