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H S Terrace

Publications and source records attributed to H S Terrace.

7 recordsLinked to original sources

Chunking during serial learning by a pigeon: III. What are the necessary conditions for establishing a chunk?

What are the minimal conditions for the formation of chunks by a pigeon learning an arbitrary list? Experiment 1 compared the acquisition of two types of chunkable list (each composed of colors and achromatic geometric forms): A----B----C----D'----E' (or A'----B'----C'----D----E) and A----B----C'----D'----E' (or A'----B'----C----D----E). The first type of list was acquired more rapidly than the second. On both lists, however, evidence of chunking did not emerge until the four-item phase of training (e.g., pauses at the end of one category of list item). In Experiment 2, chunking was shown to occur on four-item lists in which colors and forms were segregated (A----B----C'----D' and A'----B'----C----D), but not on lists in which the two types of items were interspersed (A----B'----C'----D and A'----B----C----D'). As in Experiment 1, evidence of chunking (pauses at chunk boundaries) did not appear until the fourth item was added.

Animals

Chunking during serial learning by a pigeon: I. Basic evidence.

Chunking by pigeons was demonstrated by comparing performance on different types of lists. Experiment 1 showed that Groups II and IV (who learned lists in which colors and achromatic geometric forms were segregated: A----B----C----D'----E' and A----B----C----D----E', respectively) executed lists more rapidly than did Group I (who learned a homogeneous list of colors: A----B----C----D----E) or Groups II and III (who learned lists consisting of unsegregated colors and forms: A----B'----C----D'----E and A----B----C'----D----E, respectively). Experiment 2 showed that Groups II and IV tolerated interruptions of the list better than did Groups I, III, and V. The accuracy of responding of Groups I, III, and V decreased as a function of the duration of the interruption and the point in the sequence at which it occurred. The performance of Group II was unaffected by interruptions; Group IV was minimally affected. These results indicate that Groups II and IV organized their lists as ordered chunks.

Animals

Chunking during serial learning by a pigeon: II. Integrity of a chunk on a new list.

Can a group of items that a pigeon chunks on one list function as such on a second list? In Experiment 1, the ordinal position of the chunk was held constant across both lists. Following training on a list of colors and achromatic geometric forms (A----B----C----D'----E'), the integrity of the color chunk [A----B----C] was maintained on a list of five colors (A----B----C----F----G) even though the basis for establishing that chunk was eliminated. The integrity of the chunk [A----B----C] was also maintained on a new list of colors and forms (A----B----C----D*----E*). In Experiment 2, the ordinal position of a chunk established on list1 (A----B----C'----D') was changed on list 2. As shown by positive transfer between lists 1 and 2, the integrity of the chunks [A----B] and [C'----D'] was maintained on lists X'----A----B----Y' and X'----C'----D'----Y', respectively. Conversely, the heterogeneous list X'----B----C'----Y' took longer to learn than the original list.

Animals

Serial learning by rhesus monkeys: I. Acquisition and retention of multiple four-item lists.

Two rhesus monkeys were trained to learn eight 4-item lists, each composed of 4 different photographs. Lists were trained in successive phases: A, A----B, A----B----C, and A----B----C----D. After List 4, retention, as measured by the method of savings, was, on average, 66% (range: 44-84%). Indeed, all 4 lists could be recalled reliably during a single session with neither a decrement in accuracy nor an increase in the latency of responding to each item. Response latencies on a subset test employing all possible 2- and 3-item subsets of each 4-item list support the hypothesis that monkeys form linear representations of a list. Latencies to Item 1 of a subset varied directly with the position of that item in the original list. On List 1, latencies to Item 2 varied directly with the number of intervening items between Item 1 and Item 2 in the original list. During the acquisition of Lists 5-8, both Ss mastered the A----B and A----B----C phases of training in the minimum number of trials possible.

Animals

Can an ape create a sentence?

More than 19,000 multisign utterances of an infant chimpanzee (Nim) were analyzed for syntactic and semantic regularities. Lexical regularities were observed in the case of two-sign combinations: particular signs (for example, more) tended to occur in a particular position. These regularities could not be attributed to memorization or to position habits, suggesting that they were structurally constrained. That conclusion, however, was invalidated by videotape analyses, which showed that most of Nim's utterances were prompted by his teacher's prior utterance, and that Nim interrupted his teachers to a much larger extent than a child interrupts an adult's speech. Signed utterances of other apes (as shown on films) revealed similar non-human patterns of discourse.

Animal Communication

Serial learning in the pigeon.

Three pigeons learned to peck four colors in a particular sequence, regardless of how these colors were positioned on four response keys and without feedback following each response. This demonstrates that serial learning is possible in subprimate animals.

Animals

Evidence for the innate basis of the hue dimension in the duckling.

Different groups of ducklings reared under sodium monochromatic light (589 nanometers) and under white light were trained to discriminate between the stimulus correlated with reinforcement (589 nanometers), and the stimulus correlated with extinction, whole value was either 570 or 610 nanometers. The peaks of subsequently obtained gradients of wavelength generalization of both groups were displaced away from the stimulus correlated with extinction. The peaks of the groups trained not to respond to 570 nanometers were located at 600 nanometers. The peaks of the groups trained not to respond to 610 nanometers were located at 580 nanometers. These results (in agreement with earlier data of Rudolph and Honig, 1972) suggest that ducklings have an innate basis for ordering stimuli of different wavelengths along the hue dimension.

Animals