682 research outputs found

    MAO-A and the EEG Recognition Memory Signal in Left Parietal Cortex

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    A key part of episodic memory, or memory for the events of our lives, is recognition memory. Recognition memory is the ability to remember previously encountered stimuli. Studies have linked recognition memory to the old/new effect, an EEG indicator of stimulus familiarity. Monoamine oxidase A (MAO-A) is an enzyme that catalyzes monoamines, leading to the depletion of norepinephrine, epinephrine, serotonin, and dopamine. MAO-A is more efficiently transcribed in individuals with a 4 repeating sequence variation (4R) of the MAO-A gene leading to less monoamine availability. As many of these monoamines have been linked to episodic memory, we hypothesized that individuals homozygous for the 4R MAO-A polymorphism would show differences in mean EEG signal amplitudes during recognition memory. EEG data was recorded as participants viewed both new words and words that had been previously presented. Our results show that mean peak amplitudes over the left parietal cortex 500-800 ms post-stimulus presentation for hits were greater than those for correct rejections, indicating the old/new effect. Critically, our results revealed an interaction between mean hit and correct rejection amplitude over the left parietal cortex and MAO-A group. Individuals homozygous for the 4R variation (the High MAO-A group) do not show an old/new effect due to increased correct rejection amplitudes. These results suggest that less monoamine availability leads to new stimuli being identified as old by the left parietal cortex

    Predicting Temporal Patterns In The Environment: Toward Primitive Mechanisms Of Learning, Memory, And Generalization

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    Across a wide range of cognitive tasks, recent experience influences subsequent behavior. For example, when individuals repeatedly perform a speeded two-alternative choice task, response latencies vary dramatically based on the immediately preceding sequence. These sequential dependencies (SDs) have been interpreted as adaptation to the statistical structure of an uncertain, changing environment (e.g., Jones & Sieck, 2003; Mozer, Kinoshita, & Shettel, 2007; Yu & Cohen, 2009), and can shed light on how individuals learn and represent structure in binary stimulus sequences. Heretofore, theories have posited that SDs arise from rapidly (exponentially) decaying memory traces of various environmental statistics (e.g., Cho et al., 2002; Yu & Cohen, 2009).

We present a series of experiments and a model that place SDs on a fundamentally different foundation. We show that: (1) decay of recent experience can follow a power function curve, not an exponential, linking the SD literature
to a rich literature on human declarative memory; (2) the simple trace-based mechanism underlying existing accounts is inadequate, but incremental memory adjustments may be explained via error correction, linking the SD literature to the rich literature on human associative learning; and (3) distinct but interacting subsystems are found in the brain that jointly predict upcoming environmental events. 

We conducted three behavioral studies with EEG recordings of individuals performing discrimination of spatial location and motion coherence. Identifying the onset of the lateralized readiness potential (LRP) in an event-related EEG analysis, we are able to decompose the total response latency into two intervals—pre and post LRP onset—and to examine SDs in stimulus and response processing separately. We find evidence for two distinct mechanisms, one reflecting incremental learning of stimulus repetition rate (i.e., the probability that successive
stimuli will match), and the other reflecting incremental learning of response baserates. The data cannot be explained by a model that assumes these rates are based on independent traces, and calls for an account in which the two rates jointly predict future stimuli via error-correction learning. 

By manipulating the autocorrelation structure of the sequences (from a positive to a negative autocorrelation, indicated on the graphs by blue and red lines, respectively), we obtained evidence for incremental learning occurring over hundreds of trials, which is parsimoniously explained by a memory with power function decay. Together, the results highlight a tension between the two broad and well established classes of trace-based memory models and learning models based on error correction. Two attempts at reconciling these approaches via modeling are discussed

    Higher-Order Associative Learning in Amnesia: Evidence from the Serial Reaction Time Task

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    W Patients with anterograde amnesia are commonly believed learning of higher-order information. Despite seemingly normal to exhibit normal implicit learning. Research with the serial learning effects on average, the results suggest that amnesic reaction time (SRT) task suggests that normal subjects can patients do not learn higher-order information as well as con-implicitly learn visuospatial sequences through a process that trol subjects. These results suggest that amnesic patients have is sensitive to higher-order information that is more complex an associative learning impairment, even when learning is im-than pairwise associations between adjacent stimuli. The pre- plicit, and that the medial temporal lobe and/or diencephalic sent research reexamined SRT learning in a group of amnesic brain areas typically damaged in cases of amnesia normally patients with a design intended to specifically address the contribute to implicit sequence learning.

    Planning guidelines for koala conservation and recovery: A guide to best planning practice

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    The information contained in the guide is a synthesis of four years research into the conservation and restoration of koala populations in fragmented landscapes of eastern Australia. The guidelines also capture a decade of practical research and planning experience by the Australian Koala Foundation in mapping koala habitat and developing koala conservation and management plans for local government areas in New South Wales. They draw on the collective knowledge of researchers who wanted to see their results put into action with practical outcomes for koala conservation

    Letter to the editor

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    In the current issue of NeuroImage (Vol 36, 2007), two Event-Related Potential (ERP) studies of recognition memory for faces are published back-to-back (Curran and Hancock, and MacKenzie and Donaldson). Both studies suggest that qualitatively distinct retrieval processes support recognition, consistent with “dual-process” models of recognition memory. However, the studies do so on the basis of apparently different results, a discrepancy that is surprising given the similarity of their designs. Here we place the studies in context, and highlight potential reasons for the discrepancy

    Midazolam, hippocampal function, and transitive inference: Reply to Greene

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    The transitive inference (TI) task assesses the ability to generalize learned knowledge to new contexts, and is thought to depend on the hippocampus (Dusek & Eichenbaum, 1997). Animals or humans learn in separate trials to choose stimulus A over B, B over C, C over D and D over E, via reinforcement feedback. Transitive responding based on the hierarchical structure A > B > C > D > E is then tested with the novel BD pair. We and others have argued that successful BD performance by animals – and even humans in some implicit studies – can be explained by simple reinforcement learning processes which do not depend critically on the hippocampus, but rather on the striatal dopamine system. We recently showed that the benzodiazepene midazolam, which is thought to disrupt hippocampal function, profoundly impaired human memory recall performance but actually enhanced implicit TI performance (Frank, O'Reilly & Curran, 2006). We posited that midazolam biased participants to recruit striatum during learning due to dysfunctional hippocampal processing, and that this change actually supported generalization of reinforcement values. Greene (2007) questions the validity of our pharmacological assumptions and argues that our conclusions are unfounded. Here we stand by our original hypothesis, which remains the most parsimonious account of the data, and is grounded by multiple lines of evidence

    Extending Local Canonical Correlation Analysis to Handle General Linear Contrasts for fMRI Data

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    Local canonical correlation analysis (CCA) is a multivariate method that has been proposed to more accurately determine activation patterns in fMRI data. In its conventional formulation, CCA has several drawbacks that limit its usefulness in fMRI. A major drawback is that, unlike the general linear model (GLM), a test of general linear contrasts of the temporal regressors has not been incorporated into the CCA formalism. To overcome this drawback, a novel directional test statistic was derived using the equivalence of multivariate multiple regression (MVMR) and CCA. This extension will allow CCA to be used for inference of general linear contrasts in more complicated fMRI designs without reparameterization of the design matrix and without reestimating the CCA solutions for each particular contrast of interest. With the proper constraints on the spatial coefficients of CCA, this test statistic can yield a more powerful test on the inference of evoked brain regional activations from noisy fMRI data than the conventional t-test in the GLM. The quantitative results from simulated and pseudoreal data and activation maps from fMRI data were used to demonstrate the advantage of this novel test statistic
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