GLOBAL TRENDS IN EDDY KINETIC ENERGY FROM SATELLITE ALTIMETRY

The temporal changes in the oceanic eddy kinetic energy (EKE) including trends and variability are presented and the dynamical mechanisms are investigated. The domain is near-global with a focus on the North Atlantic, North Pacific and Southern Oceans. Altimeter-derived geostrophic surface velocities are used to compute an 18 year time series of EKE on a 1/3� grid. Linear trends are best-fit to the 18-year time series and their statistical significance assessed using bootstrap techniques. Near-global mean EKE trends are non-statistically significant. However, on a regional scale, statistically significant trends are found in all of the major ocean basins. Widespread negative trends occur primarily in the northern and southern subtropical Pacific as well as the central North Atlantic, while positive trends occur primarily in the North Atlantic subtropical gyre, much of the northeast North Atlantic, the southeast Indian Ocean and in several regions in the Southern Ocean. Buoyancy forcing and non-local wind forcing related to the PDO are significant in the North Pacific. In the North Atlantic, changes in wind stress curl as well as changes in local wind speed are implicated, where a di-polar pattern of correlations with the NAO is observed. In the Southern Ocean, changes in local and/or remote winds appear as the dominant mechanism south of 30�S. On a global scale, EKE trends are slightly positive (0.15% of the mean per decade) but non-statistically significant. EKE has decreased in the northern hemisphere and increased in the southern hemisphere despite an increase in hemispheric mean wind speed in both northern and southern hemispheres. Changing wind speeds are influential across all the ocean basins but other mechanisms are significant including shifting wind stress curl fields, buoyancy forcing, indirect (non-local) winds and intrinsic variability. Statistically significant correlations between annual mean EKE and major modes of climate variability are evident in all the ocean basins

Positive impact of pre-stroke surgery on survival following transient focal ischemia in hypertensive rats

We describe a positive influence of pre-stroke surgery on recovery and survival in a commonly used experimental stroke model. Two groups of male, stroke-prone spontaneously hypertensive rats (SHRSPs) underwent transient middle cerebral artery occlusion (tMCAO). Group 1 underwent the procedure without any prior intervention whilst group 2 had an additional general anaesthetic 6 days prior to tMCAO for a cranial burrhole and durotomy. Post-stroke recovery was assessed using a 32 point neurological deficit score and tapered beam walk and infarct volume determined from haematoxylin–eosin stained sections. In group 2 survival was 92% (n = 12) versus 67% in group 1 (n = 18). In addition, post-tMCAO associated weight loss was significantly reduced in group 2. There was no significant difference between the two groups in experimental outcomes: infarct volume (Group 1 317 ± 18.6 mm<sup>3</sup> versus Group 2 332 ± 20.4 mm<sup>3</sup>), and serial (day 0–14 post-tMCAO) neurological deficit scores and tapered-beam walk test. Drilling a cranial burrhole under general anaesthesia prior to tMCAO in SHRSP reduced mortality and gave rise to infarct volumes and neurological deficits similar to those recorded in surviving Group 1 animals. This methodological refinement has significant implications for animal welfare and group sizes required for intervention studies

Constraints on the Thermal Contents of the X-Ray Cavities of Cluster MS 0735.6+7421 with Sunyaev–Zel’dovich Effect Observations

Outbursts from active galactic nuclei (AGN) can inflate cavities in the intracluster medium (ICM) of galaxy clusters and are believed to play the primary role in offsetting radiative cooling in the ICM. However, the details of how the energy from AGN feedback thermalizes to heat the ICM is not well understood, partly due to the unknown composition and energetics of the cavities. The Sunyaev–Zel'dovich (SZ) effect, a measure of the integrated pressure along the line of sight, provides a means of measuring the thermal contents of the cavities, to discriminate between thermal, nonthermal, and other sources of pressure support. Here we report measurements of the SZ effect at 30 GHz toward the galaxy cluster MS 0735.6+7421 (MS0735), using the Combined Array for Research in Millimeter-wave Astronomy (CARMA). MS0735 hosts the most energetic AGN outburst known and lobes of radio synchrotron emission coincident with a pair of giant X-ray cavities ~200 kpc across. Our CARMA maps show a clear deficit in the SZ signal coincident with the X-ray identified cavities, when compared to a smooth X-ray derived pressure model. We find that the cavities have very little SZ-contributing material, suggesting that they are either supported by very diffuse thermal plasma with temperature in excess of hundreds of keV, or are not supported thermally. Our results represent the first detection (with 4.4σ significance) of this phenomenon with the SZ effect

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

The rapid and continuing progress in gene discovery for complex diseases is fuelling interest in the potential application of genetic risk models for clinical and public health practice. The number of studies assessing the predictive ability is steadily increasing, but they vary widely in completeness of reporting and apparent quality. Transparent reporting of the strengths and weaknesses of these studies is important to facilitate the accumulation of evidence on genetic risk prediction. A multidisciplinary workshop sponsored by the Human Genome Epidemiology Network developed a checklist of 25 items recommended for strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS), building on the principles established by prior reporting guidelines. These recommendations aim to enhance the transparency, quality and completeness of study reporting, and thereby to improve the synthesis and application of information from multiple studies that might differ in design, conduct or analysis

Consequences Matter : Compassion in Conservation Means Caring for Individuals, Populations and Species

Funding This research received no external funding. Acknowledgments The manuscript benefitted from significant input from Dan Brockington, J.B. Callicott, Peter Coals, Tim Hodgetts, David Macdonald and Jeremy Wilson. Conflicts of Interest The authors declare no conflict of interest.Peer reviewedPublisher PD

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Most common human traits and diseases have a polygenic pattern of inheritance: DNA sequence variants at many genetic loci influence the phenotype. Genome-wide association (GWA) studies have identified more than 600 variants associated with human traits, but these typically explain small fractions of phenotypic variation, raising questions about the use of further studies. Here, using 183,727 individuals, we show that hundreds of genetic variants, in at least 180 loci, influence adult height, a highly heritable and classic polygenic trait. The large number of loci reveals patterns with important implications for genetic studies of common human diseases and traits. First, the 180 loci are not random, but instead are enriched for genes that are connected in biological pathways (P = 0.016) and that underlie skeletal growth defects (P < 0.001). Second, the likely causal gene is often located near the most strongly associated variant: in 13 of 21 loci containing a known skeletal growth gene, that gene was closest to the associated variant. Third, at least 19 loci have multiple independently associated variants, suggesting that allelic heterogeneity is a frequent feature of polygenic traits, that comprehensive explorations of already-discovered loci should discover additional variants and that an appreciable fraction of associated loci may have been identified. Fourth, associated variants are enriched for likely functional effects on genes, being over-represented among variants that alter amino-acid structure of proteins and expression levels of nearby genes. Our data explain approximately 10% of the phenotypic variation in height, and we estimate that unidentified common variants of similar effect sizes would increase this figure to approximately 16% of phenotypic variation (approximately 20% of heritable variation). Although additional approaches are needed to dissect the genetic architecture of polygenic human traits fully, our findings indicate that GWA studies can identify large numbers of loci that implicate biologically relevant genes and pathways.

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

Genes underneath signals from genome-wide association studies (GWAS) for kidney function are promising targets for functional studies, but prioritizing variants and genes is challenging. By GWAS meta-analysis for creatinine-based estimated glomerular filtration rate (eGFR) from the Chronic Kidney Disease Genetics Consortium and UK Biobank (n = 1,201,909), we expand the number of eGFRcrea loci (424 loci, 201 novel; 9.8% eGFRcrea variance explained by 634 independent signal variants). Our increased sample size in fine-mapping (n = 1,004,040, European) more than doubles the number of signals with resolved fine-mapping (99% credible sets down to 1 variant for 44 signals, ≤5 variants for 138 signals). Cystatin-based eGFR and/or blood urea nitrogen association support 348 loci (n = 460,826 and 852,678, respectively). Our customizable tool for Gene PrioritiSation reveals 23 compelling genes including mechanistic insights and enables navigation through genes and variants likely relevant for kidney function in human to help select targets for experimental follow-up

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Penetrance of variants in monogenic disease and clinical utility of common polygenic variation has not been well explored on a large-scale. Here, the authors use exome sequencing data from 77,184 individuals to generate penetrance estimates and assess the utility of polygenic variation in risk prediction of monogenic variants

Christianity as Public Religion::A Justification for using a Christian Sociological Approach for Studying the Social Scientific Aspects of Sport

The vast majority of social scientific studies of sport have been secular in nature and/or have tended to ignore the importance of studying the religious aspects of sport. In light of this, Shilling and Mellor (2014) have sought to encourage sociologists of sport not to divorce the ‘religious’ and the ‘sacred’ from their studies. In response to this call, the goal of the current essay is to explore how the conception of Christianity as ‘public religion’ can be utilised to help justify the use of a Christian sociological approach for studying the social scientific aspects of sport. After making a case for Christianity as public religion, we conclude that many of the sociological issues inherent in modern sport are an indirect result of its increasing secularisation and argue that this justifies the need for a Christian sociological approach. We encourage researchers to use the Bible, the tools of Christian theology and sociological concepts together, so to inform analyses of modern sport from a Christian perspective