1,412 research outputs found

    Attention and memory bias for positive emotional words

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    The current study examined the relationship between attention and memory for emotional words. Theories of basic emotion divide emotions into positive and negative classifications, and propose that discrete categories exist within the larger positive negative dichotomy. Previous research on emotion has yet to investigate the areas of attention and memory by dividing positive/negative words into discrete emotional categories. Participants included 30 undergraduate students between the ages 18--40. Attention and Memory were examined using an Emotional Stroop task, The Emotional Verbal Learning Test, and the California Verbal Learning Test-II, respectively. Stimuli for emotional tasks are divided into five emotional word categories of: happiness, sadness, anger, anxiety, and disgust. Results support the existence of the Pollyanna Principle in memory and attention; however, attention and memory were not significantly correlated within discrete emotion conditions

    Positive emotion processing deficits in schizophrenia

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    Affective impairments were examined in patients with and without deficit syndrome schizophrenia. A battery of tests designed to measure emotional experience, emotional information processing, and emotional perception were administered to deficit (n = 15) and non-deficit syndrome (n = 26) schizophrenia patients classified according to the Schedule for the Deficit Syndrome, and matched non-patient control subjects (n = 22). As predicted, in comparison to non-deficit patients and controls, deficit syndrome patients reported less frequent and intense experience of positive emotion, recalled significantly fewer positive words, and displayed an impaired ability to accurately identify and judge the valence of pleasant odors. Additionally, deficit patients demonstrated a unique failure to have their attention captured by positive information, as well as less accurate and efficient labeling of positive faces than non-deficit patients or controls. Abnormalities were also associated with negative emotions, such that deficit syndrome patients demonstrated impairment at identifying fearful faces, were less accurate at judging negative smells, had a bias toward recalling anger words, and displayed an elevated attentional lingering effect for negative information. These findings indicate that the deficit syndrome is associated with affective disturbances that impact a number of cognitive and sensory domains, and provide support for the notion that abnormalities may be most severe in relation to the experience and processing of positive emotions. These abnormalities may be due to a mood-congruent processing abnormality, and are consistent with the notion that frontal and limbic system dysfunction may be core to deficit syndrome schizophrenia

    Shorter fixation durations for up-directed saccades during saccadic exploration: A meta-analysis

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    Utilizing 23 datasets, we report a meta-analysis of an asymmetry in presaccadic fixation durations for saccades directed above and below eye fixation during saccadic exploration. For inclusion in the meta-analysis, saccadic exploration of complex visual displays had to have been made without gaze-contingent manipulations. Effect sizes for the asymmetry were quantified as Hedge’s g. Pooled effect sizes indicated significant asymmetries such that during saccadic exploration in a variety of tasks, presaccadic fixation durations for saccades directed into the upper visual field were reliably shorter than presaccadic fixation durations for saccades into the lower visual field. It is contended that the asymmetry is robust and important for efforts aimed at modelling when a saccade is initiated as a function of ensuing saccade direction

    Avolition as the core negative symptom in schizophrenia: relevance to pharmacological treatment development

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    Negative symptoms have long been considered a core component of schizophrenia. Modern conceptualizations of the structure of negative symptoms posit that there are at least two broad dimensions (motivation and pleasure and diminished expression) or perhaps five separable domains (avolition, anhedonia, asociality, blunted affect, alogia). The current review synthesizes a body of emerging research indicating that avolition may have a special place among these dimensions, as it is generally associated with poorer outcomes and may have distinct neurobiological mechanisms. Network analytic findings also indicate that avolition is highly central and interconnected with the other negative symptom domains in schizophrenia, and successfully remediating avolition results in global improvement in the entire constellation of negative symptoms. Avolition may therefore reflect the most critical treatment target within the negative symptom construct. Implications for targeted treatment development and clinical trial design are discussed

    Spectroscopy of Quasar Candidates from SDSS Commissioning Data

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    The Sloan Digital Sky Survey has obtained images in five broad-band colors for several hundred square degrees. We present color-color diagrams for stellar objects, and demonstrate that quasars are easily distinguished from stars by their distinctive colors. Follow-up spectroscopy in less than ten nights of telescope time has yielded 22 new quasars, 9 of them at z>3.65z> 3.65, and one with z=4.75z = 4.75, the second highest-redshift quasar yet known. Roughly 80% of the high-redshift quasar candidates selected by color indeed turn out to be high-redshift quasars.Comment: 4 pages, 3 figures, to appear in the proceedings of "After the Dark Ages: When Galaxies were Young (the Universe at 2<z<5)", 9th Annual October Astrophysics Conference in Marylan

    A spectroscopic study of NGC 6251 and its companion galaxies

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    Measurements of the velocities of galaxies thought to be associated with the giant radio galaxy NGC 6251 confirm the presence of a poor cluster with a systemic redshift of z= 0.0244 +/- 0.0004 and a line-of-sight velocity dispersion of sigma_{z}= 283 (+109, -52) km/s. This suggests a cluster atmosphere temperature of T = 0.7 (+0.6, -0.2) keV, which is not enough to confine the radio jet by gas pressure. The core of NGC 6251 shows strong emission lines of [O III] and H alpha + [N II], but there is no evidence for line emission from the jet (detected in optical continuum by Keel (1988)).Comment: 7 pages, 2 figures, to be published in MNRA

    MaxEnt power spectrum estimation using the Fourier transform for irregularly sampled data applied to a record of stellar luminosity

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    The principle of maximum entropy is applied to the spectral analysis of a data signal with general variance matrix and containing gaps in the record. The role of the entropic regularizer is to prevent one from overestimating structure in the spectrum when faced with imperfect data. Several arguments are presented suggesting that the arbitrary prefactor should not be introduced to the entropy term. The introduction of that factor is not required when a continuous Poisson distribution is used for the amplitude coefficients. We compare the formalism for when the variance of the data is known explicitly to that for when the variance is known only to lie in some finite range. The result of including the entropic measure factor is to suggest a spectrum consistent with the variance of the data which has less structure than that given by the forward transform. An application of the methodology to example data is demonstrated.Comment: 15 pages, 13 figures, 1 table, major revision, final version, Accepted for publication in Astrophysics & Space Scienc

    Differences in Negative Symptom Severity Across Bipolar Disorder With and Without Psychosis

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    There was no significant difference between BP+ and BP- groups. Significant difference were found in BP+ and SZ groups when tested for Affective Flattening and Alogia.Significant difference were found in HC and BP- when tested for Anhedonia-Asociality.https://digitalscholarship.unlv.edu/durep_posters/1129/thumbnail.jp

    The Vaginal Microbiome: Disease, Genetics and the Environment

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    The vagina is an interactive interface between the host and the environment. Its surface is covered by a protective epithelium colonized by bacteria and other microorganisms. The ectocervix is nonsterile, whereas the endocervix and the upper genital tract are assumed to be sterile in healthy women. Therefore, the cervix serves a pivotal role as a gatekeeper to protect the upper genital tract from microbial invasion and subsequent reproductive pathology. Microorganisms that cross this barrier can cause preterm labor, pelvic inflammatory disease, and other gynecologic and reproductive disorders. Homeostasis of the microbiome in the vagina and ectocervix plays a paramount role in reproductive health. Depending on its composition, the microbiome may protect the vagina from infectious or non-infectious diseases, or it may enhance its susceptibility to them. Because of the nature of this organ, and the fact that it is continuously colonized by bacteria from birth to death, it is virtually certain that this rich environment evolved in concert with its microbial flora. Specific interactions dictated by the genetics of both the host and microbes are likely responsible for maintaining both the environment and the microbiome. However, the genetic basis of these interactions in both the host and the bacterial colonizers is currently unknown. _Lactobacillus_ species are associated with vaginal health, but the role of these species in the maintenance of health is not yet well defined. Similarly, other species, including those representing minor components of the overall flora, undoubtedly influence the ability of potential pathogens to thrive and cause disease. Gross alterations in the vaginal microbiome are frequently observed in women with bacterial vaginosis, but the exact etiology of this disorder is still unknown. There are also implications for vaginal flora in non-infectious conditions such as pregnancy, pre-term labor and birth, and possibly fertility and other aspects of women&#x2019;s health. Conversely, the role of environmental factors in the maintenance of a healthy vaginal microbiome is largely unknown. To explore these issues, we have proposed to address the following questions:&#xd;&#xa;&#xd;&#xa;*1.&#x9;Do the genes of the host contribute to the composition of the vaginal microbiome?* We hypothesize that genes of both host and bacteria have important impacts on the vaginal microbiome. We are addressing this question by examining the vaginal microbiomes of mono- and dizygotic twin pairs selected from the over 170,000 twin pairs in the Mid-Atlantic Twin Registry (MATR). Subsequent studies, beyond the scope of the current project, may investigate which host genes impact the microbial flora and how they do so.&#xd;&#xa;*2.&#x9;What changes in the microbiome are associated with common non-infectious pathological states of the host?* We hypothesize that altered physiological (e.g., pregnancy) and pathologic (e.g., immune suppression) conditions, or environmental exposures (e.g., antibiotics) predictably alter the vaginal microbiome. Conversely, certain vaginal microbiome characteristics are thought to contribute to a woman&#x2019;s risk for outcomes such as preterm delivery. We are addressing this question by recruiting study participants from the ~40,000 annual clinical visits to women&#x2019;s clinics of the VCU Health System.&#xd;&#xa;*3.&#x9;What changes in the vaginal microbiome are associated with relevant infectious diseases and conditions?* We hypothesize that susceptibility to infectious disease (e.g. HPV, _Chlamydia_ infection, vaginitis, vaginosis, etc.) is impacted by the vaginal microbiome. In turn, these infectious conditions clearly can affect the ability of other bacteria to colonize and cause pathology. Again, we are exploring these issues by recruiting participants from visitors to women&#x2019;s clinics in the VCU Health System.&#xd;&#xa;&#xd;&#xa;Three kinds of sequence data are generated in this project: i) rDNA sequences from vaginal microbes; ii) whole metagenome shotgun sequences from vaginal samples; and iii) whole genome shotgun sequences of bacterial clones selected from vaginal samples. The study includes samples from three vaginal sites: mid-vaginal, cervical, and introital. The data sets also include buccal and perianal samples from all twin participants. Samples from these additional sites are used to test the hypothesis of a per continuum spread of bacteria in relation to vaginal health. An extended set of clinical metadata associated with these sequences are deposited with dbGAP. We have currently collected over 4,400 samples from ~100 twins and over 450 clinical participants. We have analyzed and deposited data for 480 rDNA samples, eight whole metagenome shotgun samples, and over 50 complete bacterial genomes. These data are available to accredited investigators according to NIH and Human Microbiome Project (HMP) guidelines. The bacterial clones are deposited in the Biodefense and Emerging Infections Research Resources Repository (&#x22;http://www.beiresources.org/&#x22;:http://www.beiresources.org/). &#xd;&#xa;&#xd;&#xa;In addition to the extensive sequence data obtained in this study, we are collecting metadata associated with each of the study participants. Thus, participants are asked to complete an extensive health history questionnaire at the time samples are collected. Selected clinical data associated with the visit are also obtained, and relevant information is collected from the medical records when available. This data is maintained securely in a HIPAA-compliant data system as required by VCU&#x2019;s Institutional Review Board (IRB). The preponderance of these data (i.e., that judged appropriate by NIH staff and VCU&#x2019;s IRB are deposited at dbGAP (&#x22;http://www.ncbi.nlm.nih.gov/gap&#x22;:http://www.ncbi.nlm.nih.gov/gap). Selected fields of this data have been identified by NIH staff as &#x2018;too sensitive&#x2019; and are not available in dbGAP. Individuals requiring access to these data fields are asked to contact the PI of this project or NIH Program Staff. &#xd;&#xa
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