Response preferences of monkeys (Macaca mulatta) within wavelength and line-tilt dimensions

Four rhesus monkeys were tested for preferences within the wavelength and line-tilt dimensions. In the case of wavelength, the response panel was back-illuminated by light of one of the following wavelengths, presented in a random manner: 470, 525, 580, and 635 nm. Similarly, the line-tilt dimension was studied, by presenting a 5 cm by 0.3 cm black bar tilted at 0, 30, 60, or 90 degrees. No preferences were found within this latter dimension; in contrast, marked wavelength preferences existed, the order of preference being 470 (most preferred), 525, 580, and 635 nm (least preferred). These response preferences were resistant to behavioral manipulation; the number of responses to blue and to red in extinction was about equal when red was used as the training stimulus, but vastly different following training on blue. These results indicate that such response preferences must be taken into account in the design of a wide variety of experiments.     

Selective interference in rhesus monkey (Macaca mulatta) intragroup agonistic episodes by age-sex class

Adult male interference in agonistic episodes is strongly biased against adolescent and adult male participants, whereas adult female interference is biased in favor of kin and in support of younger animals against older animals. Although natal males also are biased in favor of their kin, their selective targeting of sexually mature males is independent of kinship. Adolescent males target adult males, but only in defense of kin. This selective interference against adolescent and adult males by adult males has the potential to profoundly modify male agonistic participation in intragroup encounters after puberty. Because female support is influenced primarily by kinship, females less consistently interfere against male agonistic participants. Adult males may therefore play an important role in the socialization of male agonistic expression.     

Rhesus monkey (Macaca mulatta) cool sensitivity measured by a signal detection method

Two rhesus monkeys were trained to detect cool stimuli (decrements in skin temperature from the adapted temperature) presented to the palm of the left hand after the skin had been preadapted to a 33°C temperature. The procedure was analogous to the signal detection “yes-no” method used with human observers. Receiver operating characteristic curves were generated by varying the a priori probability of stimulus oecurrence. The proportion of hits and of false alarms increased with increases in the a priori probability of stimulation. The points of isosensitivity of both subjects for cool intensities of 0.3°C, but not at greater intensities, yielded straight lines with slopes of approximately one when plotted on normal-normal coordinates. The values of the d’_s detectability index decreased from 3.52 to 0.75 for one subject and from 2.81 1to 1.28 for the other as the stimulus intensity was decreased from 0.8° to 0.15° cooling from the adapting temperature. Cool thresholds for each subject of 0.19° and 0.12°C were computed from classical psychometric functions when threshold was defined as 50% hits at a 50% probability of stimulus occurrence. These thresholds are comparable to published reports of the cool threshold for the rhesus.     

Prototype abstraction by monkeys (Macaca mulatta)

The authors analyze the shape categorization of rhesus monkeys (Macaca mulatta) and the role of prototype- and exemplar-based comparison processes in monkeys' category learning. Prototype and exemplar theories make contrasting predictions regarding performance on the Posner-Homa dot-distortion categorization task. Prototype theory--which presumes that participants refer to-be-categorized items to a representation near the category's center (the prototype)--predicts steep typicality gradients and large prototype-enhancement effects. Exemplar theory--which presumes that participants refer to-be-categorized items to memorized training exemplars-predicts flat typicality gradients and small prototype-enhancement effects. Across many categorization tasks that, for the first time, assayed monkeys' dot-distortion categorization, monkeys showed steep typicality gradients and large prototype-enhancement effects. These results suggest that monkeys--like humans--refer to-be-categorized items to a prototype-like representation near the category's center rather than to a set of memorized training exemplars.     

Matching visual stimuli on the basis of global and local features by chimpanzees (Pan troglodytes) and rhesus monkeys (Macaca mulatta)

This study was designed to examine whether chimpanzees and monkeys exhibit a global-to-local precedence in the processing of hierarchically organized compound stimuli, as has been reported for humans. Subjects were tested using a sequential matching-to-sample paradigm using stimuli that differed on the basis of their global configuration or local elements, or on both perceptual attributes. Although both species were able to discriminate stimuli on the basis of their global configuration or local elements, the chimpanzees exhibited a global-to-local processing strategy, whereas the rhesus monkeys exhibited a local-to-global processing strategy. The results suggest that perceptual and attentional mechanisms underlying information-processing strategies may account for differences in learning by primates. Accepted after revision: 11 September 2001 Electronic Publication     

Rhesus monkeys (Macaca mulatta) immediately generalize the uncertain response

Rhesus monkeys (Macaca mulatta) have learned, like humans, to use an uncertain response adaptively under test conditions that create uncertainty, suggesting a metacognitive process by which human and nonhuman primates may monitor their confidence and alter their behavior accordingly. In this study, 4 rhesus monkeys generalized their use of the uncertain response, without additional training, to 2 familiar tasks (2-choice discrimination learning and mirror-image matching to sample) that predictably and demonstrably produce uncertainty. The monkeys were significantly less likely to use the uncertain response on trials in which the answer might be known. These results indicate that monkeys, like humans, know when they do not know and that they can learn to use a symbol as a generalized means for indicating their uncertainty.     

Salience of caller identity in rhesus monkey (Macaca mulatta) coos and screams: perceptual experiments with human (Homo sapiens) listeners

Recent evidence from acoustic analysis and playback experiments indicates that adult female rhesus monkey (Macaca mulatta) coos are individually distinctive but their screams are not. In this study, the authors compared discrimination of individual identity in these sounds by naive human listeners who judged whether 2 sounds had been produced by the same monkey or 2 monkeys. Each of 3 experiments using this same-different design showed significantly better discrimination of vocalizer identity from coos than from screams. Experiment 1 demonstrated the basic finding. Experiment 2 also tested the effect of non-identity-related scream variation, and Experiment 3 added a comparison with human vowel sounds. Outcomes suggest that acoustic structural differences in coos and screams influence salience of caller-identity cues, with significant implications for understanding the functions of these calls.     

Retrospective and prospective metacognitive judgments in rhesus macaques (Macaca mulatta)

A growing body of research suggests that some non-human animals are capable of making accurate metacognitive judgments. In previous studies, non-human animals have made either retrospective or prospective judgments (about how they did on a test or how they will do on a test, respectively). These two types of judgments are dissociable in humans. The current study tested the abilities of two rhesus macaque monkeys to make both retrospective and prospective judgments about their performance on the same memory task. Both monkeys had been trained previously to make retrospective confidence judgments. Both monkeys successfully demonstrated transfer of retrospective metacognitive judgments to the new memory task. Furthermore, both monkeys transferred their retrospective judgments to the prospective task (one, immediately, and one, following the elimination of a response bias). This study is the first to demonstrate both retrospective and prospective monitoring abilities in the same monkeys and on the same task, suggesting a greater level of flexibility in animals’ metacognitive monitoring abilities than has been reported previously.     

Perceptual completion in rhesus monkeys (Macaca mulatta) and pigeons (Columbia livia)

In a two-dimensional drawing, when the narrow edge of a bar appears to touch the edge of a large rectangle, humans overestimate the length of the bar (Kanizsa, 1979). Kanizsa has suggested that this illusion occurs because humans perceive the bar as continuing behind the rectangle and complete the "occluded" portion of the bar. Rhesus monkeys and pigeons were trained to classify black target bars with a variety of lengths as "long" or "short." In training, the bar was always located at the same distance from a gray box. After learning this discrimination, the subjects were tested on novel stimuli, in which the bar was located at three new locations. Monkeys showed a consistent response bias for "long" when the bar touched the box, but pigeons did not. Monkeys appear to have completed the "occluded" part like humans, whereas pigeons failed to do so. Because this procedure does not require animals to complete the "occluded" part with any particular form, their failure suggests that pigeons do not even perceive the target bar as continuing behind the "occluding" figure. The failure of pigeons may be due to difficulty in perceiving depth from two-dimensional drawings.     

Perceptual completion in rhesus monkeys (Macaca mulatta) and pigeons (Columba livia)

In a two-dimensional drawing, when the narrow edge of a bar appears to touch the edge of a large rectangle, humans overestimate the length of the bar (Kanizsa, 1979). Kanizsa has suggested that this illusion occurs because humans perceive the bar as continuing behind the rectangle and complete the “occluded” portion of the bar. Rhesus monkeys and pigeons were trained to classify black target bars with a variety of lengths as “long” or “short.” In training, the bar was always located at the same distance from a gray box. After learning this discrimination, the subjects were tested on novel stimuli, in which the bar was located at three new locations. Monkeys showed a consistent response bias for “long” when the bar touched the box, but pigeons did not. Monkeys appear to have completed the “occluded” part like humans, whereas pigeons failed to do so. Because this procedure does not require animals to complete the “occluded” part with any particular form, their failure suggests that pigeons do not even perceive the target bar as continuing behind the “occluding” figure. The failure of pigeons may be due to difficulty in perceiving depth from two-dimensional drawings.     

Testing visual short-term memory of pigeons (Columba livia) and a rhesus monkey (Macaca mulatta) with a location change detection task

Change detection is commonly used to assess capacity (number of objects) of human visual short-term memory (VSTM). Comparisons with the performance of non-human animals completing similar tasks have shown similarities and differences in object-based VSTM, which is only one aspect (“what”) of memory. Another important aspect of memory, which has received less attention, is spatial short-term memory for “where” an object is in space. In this article, we show for the first time that a monkey and pigeons can be accurately trained to identify location changes, much as humans do, in change detection tasks similar to those used to test object capacity of VSTM. The subject’s task was to identify (touch/peck) an item that changed location across a brief delay. Both the monkey and pigeons showed transfer to delays longer than the training delay, to greater and smaller distance changes than in training, and to novel colors. These results are the first to demonstrate location-change detection in any non-human species and encourage comparative investigations into the nature of spatial and visual short-term memory.     

Effects of competition on video-task performance in monkeys (Macaca mulatta)

The effects of competition on performance of a video-formatted task were examined in a series of experiments. Two rhesus monkeys (Macaca mulatta) were trained to manipulate a joystick to shoot at moving targets on a computer screen. The task was made competitive by requiring both animals to shoot at the same target and by rewarding only the animal that hit the target first each trial. The competitive task produced a significant and robust speed-accuracy trade-off in performance. The monkeys hit the target in significantly less time on contested than on uncontested trials. However, they required significantly more shots to hit the target on contested trials in relation to uncontested trials. This effect was unchanged when various schedules of reinforcement were introduced in the uncontested trials. This supports the influence of competition qua competition on performance, a point further bolstered by other findings of of behavioral contrast presented here.     

Weber's Law influences numerical representations in rhesus macaques (Macaca mulatta)

We present the results of two experiments that probe the ability of rhesus macaques to match visual arrays based on number. Three monkeys were first trained on a delayed match-to-sample paradigm (DMTS) to match stimuli on the basis of number and ignore continuous dimensions such as element size, cumulative surface area, and density. Monkeys were then tested in a numerical bisection experiment that required them to indicate whether a sample numerosity was closer to a small or large anchor value. Results indicated that, for two sets of anchor values with the same ratio, the probability of choosing the larger anchor value systematically increased with the sample number and the psychometric functions superimposed. A second experiment employed a numerical DMTS task in which the choice values contained an exact numerical match to the sample and a distracter that varied in number. Both accuracy and reaction time were modulated by the ratio between the correct numerical match and the distracter, as predicted by Weber's Law.