The data suggest that older workers as compared with younger ones are impaired in tasks requiring WM, which is accompanied by enhanced cardiovascular "costs" in terms of increased SBP and reduced vagal control over HR.
The after-effects of nocturnal traffic noise on cognitive performance and inhibitory brain activity were investigated. Twenty participants (18-30 years) performed an easy and a difficult visual Go/Nogo task with simultaneous EEG recording after a quiet night and then during three nights when aircraft noise was presented with equivalent noise levels of 39, 44, and 50 dBA, respectively, between 11 p.m. to 7 a.m. Based on subjective sleep quality rating, participants were separated into "good" versus "bad" sleepers. The performance and inhibition-related components (N2, P3) of event-related potentials were analysed. The N2 and P3 amplitudes were smaller and latencies were prolonged in the difficult than in the easy task. This effect was more pronounced for Nogo than for Go trials. The Nogo-P3 amplitude was smaller in Noise than in "Quiet" conditions in the difficult task only. In the difficult task, the Nogo-P3 latency was prolonged in bad sleepers than in good sleepers. The Nogo-P3 amplitude was reduced in Noise as compared to "Quiet" conditions in bad sleepers only. Sleep quality in bad sleepers worsened steadily with increasing noise levels. No effects of noise or subjective sleep quality on performance were found. Inhibitory processes appear to be selectively impaired after nocturnal noise exposure. The task difficulty and perceived sleep quality are important factors modulating noise effects. The results suggest that nocturnal traffic noise increase physiological costs for inhibitory functioning on the day even if no overt performance decrement is observed.
The study investigated the neuronal mechanisms of age-related changes in mixing costs during memory-based task switching with two levels of working memory (WM) load. Forty-eight healthy younger and 45 healthy older participants performed a memory based (high WM load) and a memory plus cue based (low WM load) switching task while event-related brain potentials (ERPs) were registered. Older adults revealed larger mixing costs in both reaction time (RT) and accuracy at higher WM loads than younger adults. The presence of explicit cues substantially reduced age differences in mixing costs for accuracy but not for RT. Similarly, no age differences regarding local switch costs were found at lower WM load. Surprisingly, larger RT local costs in younger adults than in older adults were found in the memory-based block. The CNV was reduced under high WM load and positively correlated with accuracy mixing costs in older adults. The target-locked occipital N1 and fronto-central P2 were larger in older adults relative to younger adults irrespective of WM load. The P2 latency reflected the pattern of switch costs observed in behavioral data. Moreover, P2 latency positively correlated with RT mixing costs in older adults. Elderly also showed a delayed N2 and a delayed and reduced P3b. The results suggest that age-related differences in mixing costs may be partially due to a less efficient task preparation and task set maintenance (CNV) in elderly. However, elderly attempted to compensate for these deficits by permanent activation of mechanisms relating to stimulus encoding (N1) and task-set retrieval (P2). Finally, the delayed fronto-central N2 as well as the delayed and reduced parietal P3b strongly suggest delays of response selection and working memory updating in elderly due to an increase in selection threshold or in response selection variability constituting the performance decline.
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