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Duration Discrimination (duration + discrimination)

Distribution by Scientific Domains

Life Sciences	80%

Selected Abstracts

Six-month-old infants use analog magnitudes to represent duration

DEVELOPMENTAL SCIENCE, Issue 5 2006
Kristy VanMarle
While many studies have investigated duration discrimination in human adults and in nonhuman animals, few have investigated this ability in infants. Here, we report findings that 6-month-old infants are able to discriminate brief durations, and, as with other animal species, their discrimination function is characterized by Weber's Law: proportionate difference rather than absolute difference between stimuli determined successful discrimination. Importantly, paralleling results found with nonhuman animals, the Weber function that we found for infants' discrimination of time is the same as that found for their discrimination of number. Infants discriminated durations of an audiovisual event differing by a 1:2 ratio, but not those differing by a 2:3 ratio, over a range of durations. This suggests that (a) in human as in nonhuman animals, the same mental mechanism may underlie the ability to measure duration as to represent number, and (b) we may share this mental mechanism with other animal species. [source]

Temporal filtering by prefrontal neurons in duration discrimination

EUROPEAN JOURNAL OF NEUROSCIENCE, Issue 11 2008
Ken-ichi Oshio
Abstract Neural imaging studies have revealed that the prefrontal cortex (PFC) participates in time perception. However, actual functional roles remain unclear. We trained two monkeys to perform a duration-discrimination task, in which two visual cues were presented consecutively for different durations ranging from 0.2 to 2.0 s. The subjects were required to choose the longer cue. We recorded single-neuron activity from the PFC while the subjects were performing the task. Responsive neurons for the first cue period were extracted and classified through a cluster analysis of firing rate curves. The neuronal activity was categorized as phasic, ramping and sustained patterns. Among them, the phasic activity was the most prevailing. Peak time of the phasic activity was broadly distributed about 0.8 s after cue onset, leading to a natural assumption that the phasic activity was related to cognitive processes. The phasic activity with constant delay after cue onset might function to filter current cue duration with the peak time. The broad distribution of the peak time would indicate that various filtering durations had been prepared for estimating C1 duration. The most frequent peak time was close to the time separating cue durations into long and short. The activity with this peak time might have had a role of filtering in attempted duration discrimination. Our results suggest that the PFC contributes to duration discrimination with temporal filtering in the cue period. [source]

A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3

GENES, BRAIN AND BEHAVIOR, Issue 6 2010
L. Addis
Despite the apparent robustness of language learning in humans, a large number of children still fail to develop appropriate language skills despite adequate means and opportunity. Most cases of language impairment have a complex etiology, with genetic and environmental influences. In contrast, we describe a three-generation German family who present with an apparently simple segregation of language impairment. Investigations of the family indicate auditory processing difficulties as a core deficit. Affected members performed poorly on a nonword repetition task and present with communication impairments. The brain activation pattern for syllable duration as measured by event-related brain potentials showed clear differences between affected family members and controls, with only affected members displaying a late discrimination negativity. In conjunction with psychoacoustic data showing deficiencies in auditory duration discrimination, the present results indicate increased processing demands in discriminating syllables of different duration. This, we argue, forms the cognitive basis of the observed language impairment in this family. Genome-wide linkage analysis showed a haplotype in the central region of chromosome 12 which reaches the maximum possible logarithm of odds ratio (LOD) score and fully co-segregates with the language impairment, consistent with an autosomal dominant, fully penetrant mode of inheritance. Whole genome analysis yielded no novel inherited copy number variants strengthening the case for a simple inheritance pattern. Several genes in this region of chromosome 12 which are potentially implicated in language impairment did not contain polymorphisms likely to be the causative mutation, which is as yet unknown. [source]