Solar Radiation Projections of Cmip5 Models for South of Brazil

The most critical factors in the acceleration of climate and environmental changes are related to the industrial development and consequently to an increase in the demand for electricity. Looking for measures that minimize impacts to the environment, alternative energy sources are gaining more and more space in the Brazilian energy matrix. Brazil presents a great solar potential for the generation of electric energy, so the knowledge of solar radiation and its characteristics are fundamental for the study of the energy use. Due to the above, this article aims to verify the climatic variability corresponding to the variations in solar radiation patterns, in the face of climate change scenarios. The database used in this research is part of the Phase 5 Intercomparison of Matching Models (CMIP5). Was used the RCP 8.5 that scenario is considered the most pessimistic for the 21st century and is consistent with no policy change to reduce emissions and strong dependence on fossil fuels. It is important, first of all, to determine its availability in order to enable the use of solar radiation as a source of energy in a given location and / or region. The climatic projections, based on the pessimistic scenario, in a 75-year period (2026-2100) showed a fall in solar radiation in all of Rio Grande do Sul, reaching 12% in the eastern region of the state. A concern with the factors that influence the pessimistic perspectives of this scenario, as it may affect a possible production of electric energy from solar radiation

Análise termogravimétrica do carvão de Bambusa tuldoides.

Diferentes espécies de bambu têm possibilidade de se tornar viaveis tecnicamente para a produção de carvão vegetal, por possuir semelhanças com as madeiras utilizadas para o mesmo fim. Existem três razões principais que contribuem para o sucesso de carvão de bambu no comércio internacional: o bambu cresce mais rápido e tem uma rotação mais curta em comparação com diferentes espécies de árvores. A termogravimetria (TGA) ou análise termogravimétrica fornece informações acerca da composição e estabilidade térmica, sendo uma técnica de análise térmica quantitativa. A metodologia adotada foi manter a temperatura ambiente de 1000 ºC, com taxa de aquecimento de 10ºC por minuto e vazão de 1 litro de gás nitrogênio por minuto. Observou-se que o carvão apresentou um grande potencial para a geração de energia limpa, se tornando uma opção de energia economicamente viável.SIMBRAS. Evento on-line, 16 a 18 de setembro de 2020

Arranjos agroflorestais recentemente implantados no Rio Grande do Sul, Brasil.

Este trabalho tem como objetivo registrar arranjos agroflorestais em desenvolvimento no sul do Rio Grande do Sul, a fim de fornecer informações para práticas e estudos futuros.Edição dos Anais do XI Congresso Brasileiro de Agroecologia, São Cristóvão, Sergipe, 2019. Ecologia de Saberes: Ciência, Cultura e Arte na Democratização dos Sistemas Agroalimentares

The St. Louis African American health-heart study: methodology for the study of cardiovascular disease and depression in young-old African Americans

BACKGROUND: Coronary artery disease (CAD) is a major cause of death and disability worldwide. Depression has complex bidirectional adverse associations with CAD, although the mechanisms mediating these relationships remain unclear. Compared to European Americans, African Americans (AAs) have higher rates of morbidity and mortality from CAD. Although depression is common in AAs, its role in the development and features of CAD in this group has not been well examined. This project hypothesizes that the relationships between depression and CAD can be explained by common physiological pathways and gene-environment interactions. Thus, the primary aims of this ongoing project are to: a) determine the prevalence of CAD and depression phenotypes in a population-based sample of community-dwelling older AAs; b) examine the relationships between CAD and depression phenotypes in this population; and c) evaluate genetic variants from serotoninP and inflammatory pathways to discover potential gene-depression interactions that contribute significantly to the presence of CAD in AAs. METHODS/DESIGN: The St. Louis African American Health (AAH) cohort is a population-based panel study of community-dwelling AAs born in 1936–1950 (inclusive) who have been followed from 2000/2001 through 2010. The AAH-Heart study group is a subset of AAH participants recruited in 2009–11 to examine the inter-relationships between depression and CAD in this population. State-of-the-art CAD phenotyping is based on cardiovascular characterizations (coronary artery calcium, carotid intima-media thickness, cardiac structure and function, and autonomic function). Depression phenotyping is based on standardized questionnaires and detailed interviews. Single nucleotide polymorphisms of selected genes in inflammatory and serotonin-signaling pathways are being examined to provide information for investigating potential gene-depression interactions as modifiers of CAD traits. Information from the parent AAH study is being used to provide population-based prevalence estimates. Inflammatory and other biomarkers provide information about potential pathways. DISCUSSION: This population-based investigation will provide valuable information on the prevalence of both depression and CAD phenotypes in this population. The study will examine interactions between depression and genetic variants as modulators of CAD, with the intent of detecting mechanistic pathways linking these diseases to identify potential therapeutic targets. Analytic results will be reported as they become available

New Insights Into the Clinical and Molecular Spectrum of the Novel CYFIP2-Related Neurodevelopmental Disorder and Impairment of the WRC-Mediated Actin Dynamics

Purpose: A few de novo missense variants in the cytoplasmic FMRP-interacting protein 2 (CYFIP2) gene have recently been described as a novel cause of severe intellectual disability, seizures, and hypotonia in 18 individuals, with p.Arg87 substitutions in the majority. Methods: We assembled data from 19 newly identified and all 18 previously published individuals with CYFIP2 variants. By structural modeling and investigation of WAVE-regulatory complex (WRC)-mediated actin polymerization in six patient fibroblast lines we assessed the impact of CYFIP2 variants on the WRC. Results: Sixteen of 19 individuals harbor two previously described and 11 novel (likely) disease-associated missense variants. We report p.Asp724 as second mutational hotspot (4/19 cases). Genotype–phenotype correlation confirms a consistently severe phenotype in p.Arg87 patients but a more variable phenotype in p.Asp724 and other substitutions. Three individuals with milder phenotypes carry putative loss-of-function variants, which remain of unclear pathogenicity. Structural modeling predicted missense variants to disturb interactions within the WRC or impair CYFIP2 stability. Consistent with its role in WRC-mediated actin polymerization we substantiate aberrant regulation of the actin cytoskeleton in patient fibroblasts. Conclusion: Our study expands the clinical and molecular spectrum of CYFIP2-related neurodevelopmental disorder and provides evidence for aberrant WRC-mediated actin dynamics as contributing cellular pathomechanism

Phenotypic and molecular insights into CASK-related disorders in males

Background: Heterozygous loss-of-function mutations in the X-linked CASK gene cause progressive microcephaly with pontine and cerebellar hypoplasia (MICPCH) and severe intellectual disability (ID) in females. Different CASK mutations have also been reported in males. The associated phenotypes range from nonsyndromic ID to Ohtahara syndrome with cerebellar hypoplasia. However, the phenotypic spectrum in males has not been systematically evaluated to date. Methods: We identified a CASK alteration in 8 novel unrelated male patients by targeted Sanger sequencing, copy number analysis (MLPA and/or FISH) and array CGH. CASK transcripts were investigated by RT-PCR followed by sequencing. Immunoblotting was used to detect CASK protein in patient-derived cells. The clinical phenotype and natural history of the 8 patients and 28 CASK-mutation positive males reported previously were reviewed and correlated with available molecular data. Results: CASK alterations include one nonsense mutation, one 5-bp deletion, one mutation of the start codon, and five partial gene deletions and duplications; seven were de novo, including three somatic mosaicisms, and one was familial. In three subjects, specific mRNA junction fragments indicated in tandem duplication of CASK exons disrupting the integrity of the gene. The 5-bp deletion resulted in multiple aberrant CASK mRNAs. In fibroblasts from patients with a CASK loss-of-function mutation, no CASK protein could be detected. Individuals who are mosaic for a severe CASK mutation or carry a hypomorphic mutation still showed detectable amount of protein. Conclusions: Based on eight novel patients and all CASK-mutation positive males reported previously three phenotypic groups can be distinguished that represent a clinical continuum: (i) MICPCH with severe epileptic encephalopathy caused by hemizygous loss-of-function mutations, (ii) MICPCH associated with inactivating alterations in the mosaic state or a partly penetrant mutation, and (iii) syndromic/nonsyndromic mild to severe ID with or without nystagmus caused by CASK missense and splice mutations that leave the CASK protein intact but likely alter its function or reduce the amount of normal protein. Our findings facilitate focused testing of the CASK gene and interpreting sequence variants identified by next-generation sequencing in cases with a phenotype resembling either of the three groups