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Relevant bibliographies by topics / Memory processing in monkeys

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Journal articles

Academic literature on the topic 'Memory processing in monkeys'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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Journal articles on the topic "Memory processing in monkeys"

1

Umeno, Marc M., and Michael E. Goldberg. "Spatial Processing in the Monkey Frontal Eye Field. II. Memory Responses." Journal of Neurophysiology 86, no. 5 (2001): 2344–52. http://dx.doi.org/10.1152/jn.2001.86.5.2344.

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Monkeys and humans can easily make accurate saccades to stimuli that appear and disappear before an intervening saccade to a different location. We used the flashed-stimulus task to study the memory processes that enable this behavior, and we found two different kinds of memory responses under these conditions. In the short-term spatial memory response, the monkey fixated, a stimulus appeared for 50 ms outside the neuron's receptive field, and from 200 to 1,000 ms later the monkey made a saccade that brought the receptive field onto the spatial location of the vanished stimulus. Twenty-eight o

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2

Fuster, Joaquín M. "More than working memory rides on long-term memory." Behavioral and Brain Sciences 26, no. 6 (2003): 737. http://dx.doi.org/10.1017/s0140525x03300160.

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Single-unit data from the cortex of monkeys performing working-memory tasks support the main point of the target article. Those data, however, also indicate that the activation of long-term memory is essential to the processing of all cognitive functions. The activation of cortical long-term memory networks is a key neural mechanism in attention (working memory is a form thereof), perception, memory acquisition and retrieval, intelligence, and language.

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Wright, A., H. Santiago, S. Sands, D. Kendrick, and R. Cook. "Memory processing of serial lists by pigeons, monkeys, and people." Science 229, no. 4710 (1985): 287–89. http://dx.doi.org/10.1126/science.9304205.

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Rapp, Peter R., Mary T. Kansky, and Jeffrey A. Roberts. "Impaired spatial information processing in aged monkeys with preserved recognition memory." NeuroReport 8, no. 8 (1997): 1923–28. http://dx.doi.org/10.1097/00001756-199705260-00026.

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5

Friedman, Harriet R., Janice D. Janas, and Patricia S. Goldman-Rakic. "Enhancement of Metabolic Activity in the Diencephalon of Monkeys Performing Working Memory Task: A 2-Deoxyglucose Study in Behaving Rhesus Monkeys." Journal of Cognitive Neuroscience 2, no. 1 (1990): 18–31. http://dx.doi.org/10.1162/jocn.1990.2.1.18.

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The 2-deoxyglucose (2-DG) method was used to study the effect of working memory processing on local cerebral glucose utilization (LCGU) in the diencephalon of the rhesus monkey. Monkeys were given [14C]2-DG while performing either one of three tasks that engaged working memory (WORK group) or one of two control tasks (CONT group) that used associative or non associative processes. The tasks of the WORK group—spatial delayed response, spatial delayed alternation, and delayed object alternation—are alike in that the information guiding a correct response changes from trial to trial and only the

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6

Gulya, Michelle, Carolyn Rovee-Collier, Lissa Galluccio, and Amy Wilk. "Memory Processing of a Serial List by Young Infants." Psychological Science 9, no. 4 (1998): 303–7. http://dx.doi.org/10.1111/1467-9280.00060.

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Serial list learning is thought to be beyond the capabilities of infants before the end of their 1st year. In separate experiments with 3- and 6-month-olds, we studied infants' memory for a serial list using a modified serial probe recognition procedure that was originally developed for monkeys and a precuing procedure that was previously used with human adults. Infants were trained with a three-item list. One day later, they were precued with one list member and tested for recognition of another. When the precue specified valid order information, infants of both ages recognized the test item;

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7

Parker, Amanda, Edward Wilding, and Colin Akerman. "The von Restorff Effect in Visual Object Recognition Memory in Humans and Monkeys: The Role of Frontal/Perirhinal Interaction." Journal of Cognitive Neuroscience 10, no. 6 (1998): 691–703. http://dx.doi.org/10.1162/089892998563103.

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This study reports the development of a new, modified delayed matching to sample (DMS) visual recognition memory task that controls the relative novelty of test stimuli and can be used in human and nonhuman primates. We report findings from normal humans and unoperated monkeys, as well as three groups of operated monkeys. In the study phase of this modified paradigm, subjects studied lists of two-dimensional visual object stimuli. In the test phase each studied object was presented again, now paired with a new stimulus (a foil), and the subject had to choose the studied item. In some lists one

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8

Wright, Anthony A., Jacquelyne J. Rivera, Jeffrey S. Katz, and Jocelyne Bachevalier. "Abstract-concept learning and list-memory processing by capuchin and rhesus monkeys." Journal of Experimental Psychology: Animal Behavior Processes 29, no. 3 (2003): 184–98. http://dx.doi.org/10.1037/0097-7403.29.3.184.

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9

Bongard, Sylvia, and Andreas Nieder. "Basic mathematical rules are encoded by primate prefrontal cortex neurons." Proceedings of the National Academy of Sciences 107, no. 5 (2010): 2277–82. http://dx.doi.org/10.1073/pnas.0909180107.

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Mathematics is based on highly abstract principles, or rules, of how to structure, process, and evaluate numerical information. If and how mathematical rules can be represented by single neurons, however, has remained elusive. We therefore recorded the activity of individual prefrontal cortex (PFC) neurons in rhesus monkeys required to switch flexibly between “greater than” and “less than” rules. The monkeys performed this task with different numerical quantities and generalized to set sizes that had not been presented previously, indicating that they had learned an abstract mathematical princ

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10

Ringo, J. L. "Brevity of processing in a mnemonic task." Journal of Neurophysiology 73, no. 4 (1995): 1712–15. http://dx.doi.org/10.1152/jn.1995.73.4.1712.

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1. A burst of from one to four current pulses of 0.2 ms at 100 Hz was administered bilaterally to medial temporal lobe areas while monkeys worked in a delayed matching-to-sample visual memory task. The brief electrical stimulation was used as a probe to determine when, around the 20 or 50 ms sample presentation, the disruption was most severe. 2. Stimulation within about 200 ms of the sample image onset severely perturbed the animals' ability subsequently to recognize that image. Identical stimulation at other times did not. 3. Thus, the processing during encoding, that is accessible to the im

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