1,577 research outputs found

    An NPZ Model with State-Dependent Delay due to Size-Structure in Juvenile Zooplankton

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    The study of planktonic ecosystems is important as they make up the bottom trophic levels of aquatic food webs. We study a closed Nutrient-Phytoplankton-Zooplankton (NPZ) model that includes size structure in the juvenile zooplankton. The closed nature of the system allows the formulation of a conservation law of biomass that governs the system. The model consists of a system of nonlinear ordinary differential equation coupled to a partial differential equation. We are able to transform this system into a system of delay differential equations where the delay is of threshold type and is state-dependent. The system of delay differential equations can be further transformed into one with fixed delay. Using the different forms of the model we perform a qualitative analysis of the solutions, which includes studying existence and uniqueness, positivity and boundedness, local and global stability, and conditions for extinction. Key parameters that are explored are the total biomass in the system and the maturity level at which the juvenile zooplankton reach maturity. Numerical simulations are also performed to verify our analytical results

    Post-training load-related changes of auditory working memory: An EEG study

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    Working memory (WM) refers to the temporary retention and manipulation of information, and its capacity is highly susceptible to training. Yet, the neural mechanisms that allow for increased performance under demanding conditions are not fully understood. We expected that post-training efficiency in WM performance modulates neural processing during high load tasks. We tested this hypothesis, using electroencephalography (EEG) (N = 39), by comparing source space spectral power of healthy adults performing low and high load auditory WM tasks. Prior to the assessment, participants either underwent a modality-specific auditory WM training, or a modality-irrelevant tactile WM training, or were not trained (active control). After a modality-specific training participants showed higher behavioral performance, compared to the control. EEG data analysis revealed general effects of WM load, across all training groups, in the theta-, alpha-, and beta-frequency bands. With increased load theta-band power increased over frontal, and decreased over parietal areas. Centro-parietal alpha-band power and central beta-band power decreased with load. Interestingly, in the high load condition a tendency toward reduced beta-band power in the right medial temporal lobe was observed in the modality-specific WM training group compared to the modality-irrelevant and active control groups. Our finding that WM processing during the high load condition changed after modality-specific WM training, showing reduced beta-band activity in voice-selective regions, possibly indicates a more efficient maintenance of task-relevant stimuli. The general load effects suggest that WM performance at high load demands involves complementary mechanisms, combining a strengthening of task-relevant and a suppression of task-irrelevant processing

    Observations on the translation process of trichostrongylid nema-todes.

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    A series of artificial faecal pats containing a mixture of eggs of Cooperia spp. and Ostertagia spp. at 500 e.p.g. were deposited on grassland every 2 weeks through the grazing season. The grassland had carried no stock for at least 10 years. Weekly larval counts on grass in the immediate surroundings of the pats indicated that larval concentrations are positively related to soil temperature and rainfall, and negatively to air temperature and radiation. Maximum numbers of larvae occurred after 9 to 10 weeks, suggesting that it can be extremely dangerous to return to pasture when the grass has regrown after a previous grazing. Faecal pats deposited in autumn were the main source of overwintered infection. The experiment may be considered as a model of a pasture grazed continuously by calves which have a constant egg excretion during the entire season. C.W.G. (Abstract retrieved from CAB Abstracts by CABI’s permission

    VTA neurons coordinate with the hippocampal reactivation of spatial experience

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    Spatial learning requires the hippocampus, and the replay of spatial sequences during hippocampal sharp wave-ripple (SPW-R) events of quiet wakefulness and sleep is believed to play a crucial role. To test whether the coordination of VTA reward prediction error signals with these replayed spatial sequences could contribute to this process, we recorded from neuronal ensembles of the hippocampus and VTA as rats performed appetitive spatial tasks and subsequently slept. We found that many reward responsive (RR) VTA neurons coordinated with quiet wakefulnessassociated hippocampal SPW-R events that replayed recent experience. In contrast, coordination between RR neurons and SPW-R events in subsequent slow wave sleep was diminished. Together, these results indicate distinct contributions of VTA reinforcement activity associated with hippocampal spatial replay to the processing of wake and SWS-associated spatial memory.National Institutes of Health (U.S.) (Grant R01-MH061976)United States. Office of Naval Research (Grant N00014-10-1-0936)National Institutes of Health (U.S.) (Grant K08-MH-81207-01A1

    VTA neurons coordinate with the hippocampal reactivation of spatial experience

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    Spatial learning requires the hippocampus, and the replay of spatial sequences during hippocampal sharp wave-ripple (SPW-R) events of quiet wakefulness and sleep is believed to play a crucial role. To test whether the coordination of VTA reward prediction error signals with these replayed spatial sequences could contribute to this process, we recorded from neuronal ensembles of the hippocampus and VTA as rats performed appetitive spatial tasks and subsequently slept. We found that many reward responsive (RR) VTA neurons coordinated with quiet wakefulness-associated hippocampal SPW-R events that replayed recent experience. In contrast, coordination between RR neurons and SPW-R events in subsequent slow wave sleep was diminished. Together, these results indicate distinct contributions of VTA reinforcement activity associated with hippocampal spatial replay to the processing of wake and SWS-associated spatial memory.National Institutes of Health (U.S.) (Grant R01-MH061976)United States. Office of Naval Research. Multidisciplinary University Research Initiative (Grant N00014-10-1-0936)National Institutes of Health (U.S.) (Mentored Grant K08-MH-81207-01A1

    Hippocampal Replay of Extended Experience

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    During pauses in exploration, ensembles of place cells in the rat hippocampus re-express firing sequences corresponding to recent spatial experience. Such “replay” co-occurs with ripple events: short-lasting (∼50–120 ms), high-frequency (∼200 Hz) oscillations that are associated with increased hippocampal-cortical communication. In previous studies, rats exploring small environments showed replay anchored to the rat's current location and compressed in time into a single ripple event. Here, we show, using a neural decoding approach, that firing sequences corresponding to long runs through a large environment are replayed with high fidelity and that such replay can begin at remote locations on the track. Extended replay proceeds at a characteristic virtual speed of ∼8 m/s and remains coherent across trains of ripple events. These results suggest that extended replay is composed of chains of shorter subsequences, which may reflect a strategy for the storage and flexible expression of memories of prolonged experience.Massachusetts Institute of Technology. Department of Brain and Cognitive Science (Singleton Fellowship)National Institutes of Health (U.S.) (grant MH061976
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