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The decay rate can be sufficiently slow such that no decay or acceleration of firing is observed for the duration of a memory period.
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Using a model mixing directed and random movements of a predator, we investigated how perception range and duration of spatial memory influence the long-term intake rate of a central place forager depending on prey spatial distribution.
While acute cortisol administration has been found to impair retrieval of emotional memories in healthy subjects, the duration of this memory impairment is still unknown.
Once again the rate of this increase is affected by the bottleneck, and may be arbitrarily slowed such that the firing rate appears bistable with respect to duration of the memory period of the task.
It has been observed in working memory experiments [27], [52] [53] that the rate of decay and/or the rate of acceleration of persistent activation adjust to the duration of the memory period.
Duration of associative memory in insects varies considerably, from minutes to months, depending on identity, age, and gender of test organism, strength of rewarding or aversive stimulus, number of training repetitions, and assay type [47].
The bottleneck can slow that rate such that the trajectory is impeded to the point that firing rate appears bistable with respect to the duration of the memory period of the task.
However, data on the duration of immune memory in immunocompromised persons are limited (4).
We found that discrimination thresholds got steadily worse with increasing duration of the memory interval.
The populations used to select mAb SD6-resistant mutants were derived from C-S8c1p100, in experiments designed to test duration of quasispecies memory [ 45].
This approach seems particularly attractive to pursue as results from learning and memory experiments have demonstrated that enhancing specific gene transcription generates a form of long-term memory that is persistent and lasts beyond the duration of normal memory [ 23, 24].
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