19 research outputs found

    Dataset for Response of the Invasive Alliaria Petiolata to Extreme Temperatures and Drought

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    Alliaria petiolata, a strict biennial in North America, can have annual alternating high abundance of rosettes and flowering plants. We monitored changes in abundance of rosettes and flowering plants in permanent plots (2004 to 2014). Three times during our study the alternating yearly cycle was not observed (2007-2008, 2008-2009, and 2013-2014). We concluded stochastic Extreme Climate Events (ECEs), deviating from long-term climatic data norms (10th or 90th. percentile), likely caused negative organism responses. Long-term data from a local NOAA station located 25 km from our study site included monthly data (1) total precipitation, (2) number of days with \u3e 0.13 cm precipitation, and (3) mean and minimum temperatures. September 2007 met criteria for ECEs for all monthly variables. We first observed A. petiolata on our study site in 1988 and by the early 1990’s it was abundant. To determine if September 2007 significantly differed from other Septembers (1984-2014) we used six variables related to drought: (1) total precipitation, (2) number of days with precipitation, (3) number of contiguous days without precipitation, (4) mean monthly temperature, (5) mean maximum daily temperature, and (6) the number of days with temperatures \u3e 30 o C. The first two variables likely increase plant stress as they decrease, whereas stress declines as the remaining variables decrease. We used the six variables to generate a Principal Component Analysis (PCA) biplot. Axes 1 and 2 accounted for 74.3% of the variance. Record-breaking minimum temperatures (ECEs) for January (2009) and February-March (2014) likely reduced rosette abundance and disrupted reestablishment of alternating high abundance of rosettes and flowering plants. Our data suggest that a single ECE variable, minimum temperature, and multiple ECE variables related to drought likely had negative effects on A. petiolata

    Do red deer stags (Cervus elaphus) use roar fundamental frequency (F0) to assess rivals?

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    It is well established that in humans, male voices are disproportionately lower pitched than female voices, and recent studies suggest that this dimorphism in fundamental frequency (F0) results from both intrasexual (male competition) and intersexual (female mate choice) selection for lower pitched voices in men. However, comparative investigations indicate that sexual dimorphism in F0 is not universal in terrestrial mammals. In the highly polygynous and sexually dimorphic Scottish red deer Cervus elaphus scoticus, more successful males give sexually-selected calls (roars) with higher minimum F0s, suggesting that high, rather than low F0s advertise quality in this subspecies. While playback experiments demonstrated that oestrous females prefer higher pitched roars, the potential role of roar F0 in male competition remains untested. Here we examined the response of rutting red deer stags to playbacks of re-synthesized male roars with different median F0s. Our results show that stags’ responses (latencies and durations of attention, vocal and approach responses) were not affected by the F0 of the roar. This suggests that intrasexual selection is unlikely to strongly influence the evolution of roar F0 in Scottish red deer stags, and illustrates how the F0 of terrestrial mammal vocal sexual signals may be subject to different selection pressures across species. Further investigations on species characterized by different F0 profiles are needed to provide a comparative background for evolutionary interpretations of sex differences in mammalian vocalizations

    Contested Ground : Why are some policies healthy and others not? : Conference Summary

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    Summary of the 2016 Centre for Health Services and Policy Research annual health policy conference.Medicine, Faculty ofPopulation and Public Health (SPPH), School ofUnreviewedFacultyResearcherPostdoctora

    Supplemental Material, SPPS784890_suppl_mat - Genetic and Environmental Associations Between Child Personality and Parenting

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    <p>Supplemental Material, SPPS784890_suppl_mat for Genetic and Environmental Associations Between Child Personality and Parenting by Mona Ayoub, Daniel A. Briley, Andrew Grotzinger, Megan W. Patterson, Laura E. Engelhardt, Jennifer L. Tackett, K. Paige Harden, and Elliot M. Tucker-Drob in Social Psychological and Personality Science</p

    Sensation seeking and impulsive traits as personality endophenotypes for antisocial behavior: Evidence from two independent samples

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    Sensation seeking and impulsivity are personality traits that are correlated with risk for antisocial behavior (ASB). This paper uses two independent samples of twins to (a) test the extent to which sensation seeking and impulsivity statistically mediate genetic influence on ASB, and (b) compare this to genetic influences accounted for by other personality traits. In Sample 1, delinquent behavior, as well as impulsivity, sensation seeking and Big Five personality traits, were measured in adolescent twins from the Texas Twin Project. In Sample 2, adult twins from the Australian Twin Registry responded to questionnaires that assessed individual differences in Eysenck's and Cloninger's personality dimensions, and a structured telephone interview that asked participants to retrospectively report DSM-de- fined symptoms of conduct disorder. Bivariate quantitative genetic models were used to identify genetic overlap between personality traits and ASB. Across both samples, novelty/sensation seeking and impulsive traits accounted for larger portions of genetic variance in ASB than other personality traits.We discuss whether sensation seeking and impulsive personality are causal endophenotypes for ASB, or merely index genetic liability for ASB

    A systematic review of regional hyperthermia therapy in bladder cancer

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    Bladder cancer therapy remains suboptimal as morbidity and mortality remain high amongst those with non-muscle-invasive and muscle-invasive disease. Regional hyperthermia therapy (RHT) is a promising adjunctive therapy being tested in multiple clinical contexts. The aim of this study was to systematically review the literature on the efficacy and toxicity of RHT. This systematic review was registered with the PROSPERO database (Registration number: CRD42015025780) and was conducted according to the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines. We queried PubMed, EMBASE, and Cochrane libraries. Two reviewers reviewed abstracts independently and a third reviewer arbitrated disagreements. The last search was performed on 28 August 2015. A descriptive analysis was performed and quality assessment was conducted using the Newcastle-Ottawa Quality Assessment Scale for observational studies, and the Cochrane Risk of Bias Assessment Tool for trials. We identified 859 publications in the initial search, of which 24 met inclusion criteria for full-text review. Of these, we were able to obtain data on the outcomes of interest for 15 publications. The review underscores the limited nature of the evidence; definitive conclusions are elusive. However, the promising results of RHT in the setting of intravesical chemotherapy, chemotherapy and radiotherapy show a trend towards legitimate efficac

    Differences between the neurogenic and proliferative abilities of Müller glia with stem cell characteristics and the ciliary epithelium from the adult human eye

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    Much controversy has arisen on the nature and sources of stem cells in the adult human retina. Whilst ciliary epithelium has been thought to constitute a source of neural stem cells, a population of Müller glia in the neural retina has also been shown to exhibit neurogenic characteristics. This study aimed to compare the neurogenic and proliferative abilities between these two major cell populations. It also examined whether differences exist between the pigmented and non-pigmented ciliary epithelium (CE) from the adult human eye. On this basis, Müller glia with stem cell characteristics and pigmented and non-pigmented CE were isolated from human neural retina and ciliary epithelium respectively. Expression of glial, epithelial and neural progenitor markers was examined in these cells following culture under adherent and non-adherent conditions and treatments to induce neural differentiation. Unlike pigmented CE which did not proliferate, non-pigmented CE cells exhibited limited proliferation in vitro, unless epidermal growth factor (EGF) was present in the culture medium to prolong their survival. In contrast, Müller glial stem cells (MSC) cultured as adherent monolayers reached confluence within a few weeks and continued to proliferative indefinitely in the absence of EGF. Both MSC and non-pigmented CE expressed markers of neural progenitors, including SOX2, PAX6, CHX10 and NOTCH. Nestin, a neural stem cell marker, was only expressed by MSC. Non-pigmented CE displayed epithelial morphology, limited photoreceptor gene expression and stained strongly for pigmented epithelial markers upon culture with neural differentiation factors. In contrast, MSC adopted neural morphology and expressed markers of retinal ganglion cells and photoreceptors when cultured under similar conditions

    Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations.

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    Germline loss-of-function mutations in the transcription factor signal transducer and activator of transcription 3 (STAT3) cause immunodeficiency, whereas somatic gain-of-function mutations in STAT3 are associated with large granular lymphocytic leukemic, myelodysplastic syndrome, and aplastic anemia. Recently, germline mutations in STAT3 have also been associated with autoimmune disease. Here, we report on 13 individuals from 10 families with lymphoproliferation and early-onset solid-organ autoimmunity associated with 9 different germline heterozygous mutations in STAT3. Patients exhibited a variety of clinical features, with most having lymphadenopathy, autoimmune cytopenias, multiorgan autoimmunity (lung, gastrointestinal, hepatic, and/or endocrine dysfunction), infections, and short stature. Functional analyses demonstrate that these mutations confer a gain-of-function in STAT3 leading to secondary defects in STAT5 and STAT1 phosphorylation and the regulatory T-cell compartment. Treatment targeting a cytokine pathway that signals through STAT3 led to clinical improvement in 1 patient, suggesting a potential therapeutic option for such patients. These results suggest that there is a broad range of autoimmunity caused by germline STAT3 gain-of-function mutations, and that hematologic autoimmunity is a major component of this newly described disorder. Some patients for this study were enrolled in a trial registered at www.clinicaltrials.gov as #NCT00001350
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