Using ⁸⁷Sr/⁸⁶Sr Ratios to Date Fossil Methane Seep Deposits: Methodological Requirements and an Example from the Great Valley Group, California

Methane seep carbonates preserve information about the history of methane seepage and of the fauna inhabiting these ecosystems. For this information to be useful, a reliable determination of the carbonates’ stratigraphic ages is required, but this is not always available. Here we investigate the using strontium isotope stratigraphy to date fossil methane seep carbonates via detailed petrographic and geochemical investigation of the different carbonate phases in biostratigraphically well-dated seep carbonates of Paleozoic, Mesozoic, and Cenozoic age. The best results are obtained from banded, botryoidal rim cements from carbonate phases showing a weak or no cathodoluminescence signal, an oxygen isotope signature close to that of seawater, and the lowest Mn concentrations. We then applied the method to a presumably late Jurassic seep carbonate from the Great Valley Group in California. Strontium isotope ratios of the least diagenetically altered carbonate phases indicate a Tithonian (late Jurassic) age for this seep site, which is in conflict with a recent study that suggested the absence of Jurassic strata from the Great Valley Group

Promoção da Qualidade das Relações Interpessoais, da Saúde e do Bem-Estar dos Enfermeiros do HFF: o Projeto, Resultados T1, e a Fase de Intervenção

Promoção da qualidade das relações interpessoais, da saúde e do bem-estar dos enfermeiros do HFF: O projeto, resultados T1 e a fase de intervenção

Increased UV transmission by improving the manufacturing process for FS

ABSTRACT Optical designers have been designing ultraviolet (UV) systems at wavelengths in the UV region for many years. With increasing demand for deep UV applications, special considerations that are not applicable to traditional visible optics must be taken to produce the optics. Specifically as the wavelength of incident light decreases, the importance of very smooth surfaces increases. The intent of this project is to increase the performance of UV optics in a four-phase project. The first phase consists of characterizing sub-surface damage using destructive methods to enable process control, the second phase (presented here) focuses on polishing methods, the third phase will include cleaning and possible etching protocols and the fourth phase will be improving thin film coating performance. Keywords: Ultraviolet, fused silica, polishing, coating INTRODUCTION As trends in UV optical system design shift to shorter UV wavelengths, optical manufacturing has to be more conscious of the effect that subsurface damage, surface features, residual contamination from polishing and cleaning and coating have on the residual performance of the optics in their systems. For many years, researchers have tackled partial aspects of these problems. For example, Bloembergen 1 stated that cracks and pores on an optical surface will lead to laser damage (LD) when incident with a laser beam. Neauport et al. 2 spoke to two of the main damage initiators of LD, sub-surface damage (SSD) and nano-absorbing centers, focusing mainly on the latter. They used fused silica optics in high power laser applications at 351nm. Higher cerium concentration on the surfaces strongly correlated with increased damage density. Aluminum, copper and iron did not have similar correlations. Neauport et al. also tried to correlate the presence of cerium with damage morphology but the results were inconclusive. Yoshiyama et al. 3 studied the effects of polishing, etching, cleaving and water leaching on the UV damage of fused silica. The surfaces were all exposed to a Nd:YAG laser at 355nm. Micropits were found on the polished surface. Their analysis found high concentrations of Al, B, Ce and Zr. The concentrations of the Al, B and Zr all decreased rapidly to less than 10% of the maximum value at a depth of 50nm, but the Ce required ~100nm before decreasing to less than 10% of its maximum value. A second sample etched with a buffered HF solution had a lower pit density than the polished surface. The pit density decreased exponentially with the etched layer thickness indicating that the cerium is a precursor to laser damage. Micropits found on the cleaved surface indicated that cerium contamination is not the only cause of damage. It is hypothesized that damage initiated because of residual stresses and permanent mechanical damage from the cleaving process. Hydrolyzed cleaved surfaces were found to decrease the laser damage threshold. Camp et al. 4 determined that the zirconia conventionally polished surfaces have a higher laser damage threshold at 355nm compared to ceria polished surfaces. They also observed that damage typically centered around scratches or digs on the surface of the parts. Néauport et al

Translational models for vascular cognitive impairment: a review including larger species.

BACKGROUND: Disease models are useful for prospective studies of pathology, identification of molecular and cellular mechanisms, pre-clinical testing of interventions, and validation of clinical biomarkers. Here, we review animal models relevant to vascular cognitive impairment (VCI). A synopsis of each model was initially presented by expert practitioners. Synopses were refined by the authors, and subsequently by the scientific committee of a recent conference (International Conference on Vascular Dementia 2015). Only peer-reviewed sources were cited. METHODS: We included models that mimic VCI-related brain lesions (white matter hypoperfusion injury, focal ischaemia, cerebral amyloid angiopathy) or reproduce VCI risk factors (old age, hypertension, hyperhomocysteinemia, high-salt/high-fat diet) or reproduce genetic causes of VCI (CADASIL-causing Notch3 mutations). CONCLUSIONS: We concluded that (1) translational models may reflect a VCI-relevant pathological process, while not fully replicating a human disease spectrum; (2) rodent models of VCI are limited by paucity of white matter; and (3) further translational models, and improved cognitive testing instruments, are required

The Chromatin Remodeling Factor SMARCB1 Forms a Complex with Human Cytomegalovirus Proteins UL114 and UL44

Background: Human cytomegalovirus (HCMV) uracil DNA glycosylase, UL114, is required for efficient viral DNA replication. Presumably, UL114 functions as a structural partner to other factors of the DNA-replication machinery and not as a DNA repair protein. UL114 binds UL44 (HCMV processivity factor) and UL54 (HCMV-DNA-polymerase). In the present study we have searched for cellular partners of UL114. Methodology/Principal Findings: In a yeast two-hybrid screen SMARCB1, a factor of the SWI/SNF chromatin remodeling complex, was found to be an interacting partner of UL114. This interaction was confirmed in vitro by coimmunoprecipitation and pull-down. Immunofluorescence microscopy revealed that SMARCB1 along with BRG-1, BAF170 and BAF155, which are the core SWI/SNF components required for efficient chromatin remodeling, were present in virus replication foci 24–48 hours post infection (hpi). Furthermore a direct interaction was also demonstrated for SMARCB1 and UL44. Conclusions/Significance: The core SWI/SNF factors required for efficient chromatin remodeling are present in the HCMV replication foci throughout infection. The proteins UL44 and UL114 interact with SMARCB1 and may participate in the recruitment of the SWI/SNF complex to the chromatinized virus DNA. Thus, the presence of the SWI/SNF chromatin remodeling complex in replication foci and its association with UL114 and with UL44 might imply its involvement i

The Worksite Health Promotion Capacity Instrument (WHPCI): development, validation and approaches for determining companies' levels of health promotion capacity

<p>Abstract</p> <p>Background</p> <p>The Worksite Health Promotion Capacity Instrument (WHPCI) was developed to assess two key factors for effective worksite health promotion: collective willingness and the systematic implementation of health promotion activities in companies. This study evaluates the diagnostic qualities of the WHPCI based on its subscales Health Promotion Willingness and Health Promotion Management, which can be used to place companies into four different categories based on their level of health promotion capacity.</p> <p>Methods</p> <p>Psychometric evaluation was conducted using exploratory factor and reliability analyses with data taken from a random sample of managers from n = 522 German information and communication technology (ICT) companies. Receiver operating characteristic (ROC) analyses were conducted to determine further diagnostic qualities of the instrument and to establish the cut-off scores used to determine each company's level of health promotion capacity.</p> <p>Results</p> <p>The instrument's subscales, Health Promotion Willingness and Health Promotion Management, are based on one-dimensional constructs, each with very good reliability (Cronbach's alpha = 0.83/0.91). ROC analyses demonstrated satisfactory diagnostic accuracy with an area under the curve (AUC) of 0.76 (SE = 0.021; 95% CI 0.72-0.80) for the Health Promotion Willingness scale and 0.81 (SE = 0.021; 95% CI 0.77-0.86) for the Health Promotion Management scale. A cut-off score with good sensitivity (71%/76%) and specificity (69%/75%) was determined for each scale. Both scales were found to have good predictive power and exhibited good efficiency.</p> <p>Conclusions</p> <p>Our findings indicate preliminary evidence for the validity and reliability of both subscales of the WHPCI. The goodness of each cut-off score suggests that the scales are appropriate for determining companies' levels of health promotion capacity. Support in implementing (systematic) worksite health promotion can then be tailored to each company's needs based on their current capacity level.</p

Epigenetic Analysis of KSHV Latent and Lytic Genomes

Epigenetic modifications of the herpesviral genome play a key role in the transcriptional control of latent and lytic genes during a productive viral lifecycle. In this study, we describe for the first time a comprehensive genome-wide ChIP-on-Chip analysis of the chromatin associated with the Kaposi's sarcoma-associated herpesvirus (KSHV) genome during latency and lytic reactivation. Depending on the gene expression class, different combinations of activating [acetylated H3 (AcH3) and H3K4me3] and repressive [H3K9me3 and H3K27me3] histone modifications are associated with the viral latent genome, which changes upon reactivation in a manner that is correlated with their expression. Specifically, both the activating marks co-localize on the KSHV latent genome, as do the repressive marks. However, the activating and repressive histone modifications are mutually exclusive of each other on the bulk of the latent KSHV genome. The genomic region encoding the IE genes ORF50 and ORF48 possesses the features of a bivalent chromatin structure characterized by the concomitant presence of the activating H3K4me3 and the repressive H3K27me3 marks during latency, which rapidly changes upon reactivation with increasing AcH3 and H3K4me3 marks and decreasing H3K27me3. Furthermore, EZH2, the H3K27me3 histone methyltransferase of the Polycomb group proteins (PcG), colocalizes with the H3K27me3 mark on the entire KSHV genome during latency, whereas RTA-mediated reactivation induces EZH2 dissociation from the genomic regions encoding IE and E genes concurrent with decreasing H3K27me3 level and increasing IE/E lytic gene expression. Moreover, either the inhibition of EZH2 expression by a small molecule inhibitor DZNep and RNAi knockdown, or the expression of H3K27me3-specific histone demethylases apparently induced the KSHV lytic gene expression cascade. These data indicate that histone modifications associated with the KSHV latent genome are involved in the regulation of latency and ultimately in the control of the temporal and sequential expression of the lytic gene cascade. In addition, the PcG proteins play a critical role in the control of KSHV latency by maintaining a reversible heterochromatin on the KSHV lytic genes. Thus, the regulation of the spatial and temporal association of the PcG proteins with the KSHV genome may be crucial for propagating the KSHV lifecycle