SPYGLASS. III. The Fornax-Horologium Association and its Traceback History within the Austral Complex

The study of young associations is essential for building a complete record of local star formation processes. The Fornax-Horologium association (FH), including the $\chi^1$ Fornacis cluster, represents one of the nearest young stellar populations to the Sun. This association has recently been linked to the Tuc-Hor, Carina, and Columba associations, building an extensive "Austral Complex" almost entirely within 150 pc. Using Gaia astrometry and photometry in addition to new spectroscopic observations, we perform the deepest survey of FH to date, identifying over 300 candidate members, nearly doubling the known population. By combining this sample with literature surveys of the other constituent populations, we produce a contiguous stellar population covering the entire Austral Complex, allowing the definitions of sub-populations to be re-assessed along with connections to external populations. This analysis recovers new definitions for FH, Tuc-Hor, Columba, and Carina, while also revealing a connection between the Austral complex and the Sco-Cen-affiliated Platais 8 cluster. This suggests that the Austral complex may be just a small component of a much larger and more diverse star formation event. Computing ages and tracing stellar populations back to formation reveals two distinct nodes of cospatial and continuous formation in the Austral Complex, one containing Tuc-Hor, and the other containing FH, Carina, and Columba. This mirrors recent work showing similar structure elsewhere, suggesting that these nodes, which only emerge through the use of traceback, may represent the clearest discrete unit of local star formation, and a key building block needed to reconstruct larger star-forming events.Comment: Accepted to ApJ; 29 pages, 10 figures, 5 tables in two-column AASTEX63 forma

The Wahlquist-Newman solution

Based on a geometrical property which holds both for the Kerr metric and for the Wahlquist metric we argue that the Kerr metric is a vacuum subcase of the Wahlquist perfect-fluid solution. The Kerr-Newman metric is a physically preferred charged generalization of the Kerr metric. We discuss which geometric property makes this metric so special and claim that a charged generalization of the Wahlquist metric satisfying a similar property should exist. This is the Wahlquist-Newman metric, which we present explicitly in this paper. This family of metrics has eight essential parameters and contains the Kerr-Newman-de Sitter and the Wahlquist metrics, as well as the whole Pleba\'nski limit of the rotating C-metric, as particular cases. We describe the basic geometric properties of the Wahlquist-Newman metric, including the electromagnetic field and its sources, the static limit of the family and the extension of the spacetime across the horizon.Comment: LaTeX, 18 pages, no figures. Accepted for publication in Phys. Rev.

Network-Based Analysis of Affected Biological Processes in Type 2 Diabetes Models

Type 2 diabetes mellitus is a complex disorder associated with multiple genetic, epigenetic, developmental, and environmental factors. Animal models of type 2 diabetes differ based on diet, drug treatment, and gene knockouts, and yet all display the clinical hallmarks of hyperglycemia and insulin resistance in peripheral tissue. The recent advances in gene-expression microarray technologies present an unprecedented opportunity to study type 2 diabetes mellitus at a genome-wide scale and across different models. To date, a key challenge has been to identify the biological processes or signaling pathways that play significant roles in the disorder. Here, using a network-based analysis methodology, we identified two sets of genes, associated with insulin signaling and a network of nuclear receptors, which are recurrent in a statistically significant number of diabetes and insulin resistance models and transcriptionally altered across diverse tissue types. We additionally identified a network of protein–protein interactions between members from the two gene sets that may facilitate signaling between them. Taken together, the results illustrate the benefits of integrating high-throughput microarray studies, together with protein–protein interaction networks, in elucidating the underlying biological processes associated with a complex disorder

SPYGLASS. II. The Multi-Generational and Multi-Origin Star Formation History of Cepheus Far North

Young stellar populations provide a record of past star formation, and by establishing their members' dynamics and ages, it is possible to reconstruct the full history of star formation events. Gaia has greatly expanded the number of accessible stellar populations, with one of the most notable recently-discovered associations being Cepheus Far North (CFN), a population containing hundreds of members spanning over 100 pc. With its proximity (d $\lesssim$ 200 pc), apparent substructure, and relatively small population, CFN represents a manageable population to study in depth, with enough evidence of internal complexity to produce a compelling star formation story. Using Gaia astrometry and photometry combined with additional spectroscopic observations, we identify over 500 candidate CFN members spread across 7 subgroups. Combining ages from isochrones, asteroseismology, dynamics, and lithium depletion, we produce well-constrained ages for all seven subgroups, revealing a largely continuous 10 Myr star formation history in the association. By tracing back the present-day populations to the time of their formation, we identify two spatially and dynamically distinct nodes in which stars form, one associated with $\beta$ Cephei which shows mostly co-spatial formation, and one associated with EE Draconis with a more dispersed star formation history. This detailed view of star formation demonstrates the complexity of the star formation process, even in the smallest of regions.Comment: Accepted to ApJ; 34 pages, 15 figures, 6 tables in two-column AASTEX63 forma

Altruism can proliferate through group/kin selection despite high random gene flow

The ways in which natural selection can allow the proliferation of cooperative behavior have long been seen as a central problem in evolutionary biology. Most of the literature has focused on interactions between pairs of individuals and on linear public goods games. This emphasis led to the conclusion that even modest levels of migration would pose a serious problem to the spread of altruism in group structured populations. Here we challenge this conclusion, by analyzing evolution in a framework which allows for complex group interactions and random migration among groups. We conclude that contingent forms of strong altruism can spread when rare under realistic group sizes and levels of migration. Our analysis combines group-centric and gene-centric perspectives, allows for arbitrary strength of selection, and leads to extensions of Hamilton's rule for the spread of altruistic alleles, applicable under broad conditions.Comment: 5 pages, 2 figures. Supplementary material with 50 pages and 26 figure

Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing:a population-based study

Background<p></p> Familial hypercholesterolaemia (FH) is a common Mendelian condition which, untreated, results in premature coronary heart disease. An estimated 88% of FH cases are undiagnosed in the UK. We previously validated a method for FH mutation detection in a lipid clinic population using next generation sequencing (NGS), but this did not address the challenge of identifying index cases in primary care where most undiagnosed patients receive healthcare. Here, we evaluate the targeted use of NGS as a potential route to diagnosis of FH in a primary care population subset selected for hypercholesterolaemia.<p></p> Methods<p></p> We used microfluidics-based PCR amplification coupled with NGS and multiplex ligation-dependent probe amplification (MLPA) to detect mutations in LDLR, APOB and PCSK9 in three phenotypic groups within the Generation Scotland: Scottish Family Health Study including 193 individuals with high total cholesterol, 232 with moderately high total cholesterol despite cholesterol-lowering therapy, and 192 normocholesterolaemic controls.<p></p> Results<p></p> Pathogenic mutations were found in 2.1% of hypercholesterolaemic individuals, in 2.2% of subjects on cholesterol-lowering therapy and in 42% of their available first-degree relatives. In addition, variants of uncertain clinical significance (VUCS) were detected in 1.4% of the hypercholesterolaemic and cholesterol-lowering therapy groups. No pathogenic variants or VUCS were detected in controls.<p></p> Conclusions<p></p> We demonstrated that population-based genetic testing using these protocols is able to deliver definitive molecular diagnoses of FH in individuals with high cholesterol or on cholesterol-lowering therapy. The lower cost and labour associated with NGS-based testing may increase the attractiveness of a population-based approach to FH detection compared to genetic testing with conventional sequencing. This could provide one route to increasing the present low percentage of FH cases with a genetic diagnosis

THE UNIQUENESS THEOREM FOR ROTATING BLACK HOLE SOLUTIONS OF SELF-GRAVITATING HARMONIC MAPPINGS

We consider rotating black hole configurations of self-gravitating maps from spacetime into arbitrary Riemannian manifolds. We first establish the integrability conditions for the Killing fields generating the stationary and the axisymmetric isometry (circularity theorem). Restricting ourselves to mappings with harmonic action, we subsequently prove that the only stationary and axisymmetric, asymptotically flat black hole solution with regular event horizon is the Kerr metric. Together with the uniqueness result for non-rotating configurations and the strong rigidity theorem, this establishes the uniqueness of the Kerr family amongst all stationary black hole solutions of self-gravitating harmonic mappings.Comment: 18 pages, latex, no figure

Penalty Corner Routines in Elite Women’s Indoor Field Hockey: Prediction of Outcomes based on Tactical Decisions

Indoor hockey is a highly competitive international sport, yet no research to date has investigated the key actions within this sport. As with outdoor field hockey, penalty corners represent one of the most likely situations in which goals can be scored. All 36 matches of the round-robin phase of the 2010-2011 England Hockey League Women’s Premier Division ‘Super Sixes’ competition were analysed with the purpose of establishing which factors can predict the scoring of a goal using Binary Logistic Regression analysis. Seventy two (22.6%) of the 319 observed penalty corners resulted in a goal. The strongest predictor of scoring a goal was taking the penalty corner from the goalkeeper’s right. Based on the odds ratio (OR), the odds of the attacking team scoring were 2.27 (CI = 1.41 - 3.65) times higher with penalty corners taken from the goalkeeper’s right as opposed to the left. Additionally, if the goalkeeper decided to rush to the edge of the circle, the odds of the attacking team failing to score were 2.19 (CI = 1.18 - 4.08) times higher compared to when the goalkeeper remained near the goal line. These results suggest that strategic decisions from the players and coaches have an important part to play in the success of penalty corners. Future research should investigate the impact of goalkeepers’ movement and further examine the technical and tactical intricacies of penalty corners

Roles and practices of general practitioners and psychiatrists in management of depression in the community

BACKGROUND: Little is known about depressed patients' profiles and how they are managed. The aim of the study is to compare GPs and psychiatrists for 1°) sociodemographic and clinical profile of their patients considered as depressed 2°) patterns of care provision. METHODS: The study design is an observational cross-sectional study on a random sample of GPs and psychiatrists working in France. Consecutive inclusion of patients seen in consultation considered as depressed by the physician. GPs enrolled 6,104 and psychiatrists 1,433 patients. Data collected: sociodemographics, psychiatric profile, environmental risk factors of depression and treatment. All clinical data were collected by participating physicians; there was no direct independent clinical assessment of patients to check the diagnosis of depressive disorder. RESULTS: Compared to patients identified as depressed by GPs, those identified by psychiatrists were younger, more often urban (10.5% v 5.4% – OR = 2.4), educated (42.4% v 25.4% – OR = 3.9), met DSM-IV criteria for depression (94.6% v 85.6% – OR = 2.9), had been hospitalized for depression (26.1% v 15.6% – OR = 2.0) and were younger at onset of depressive problems (all adjusted p < .001). No difference was found for psychiatric and somatic comorbidity, suicide attempt and severity of current depression. Compared to GPs, psychiatrists more often prescribed tricyclics and very novel antidepressants (7.8% v 2.3% OR = 5.0 and 6.8% v 3.0% OR = 3.8) with longer duration of antidepressant treatment. GPs' patients received more "non-conventional" treatment (8.8% v 2.4% OR = 0.3) and less psychotherapy (72.2% v 89.1% OR = 3.1) (all adjusted p < .001). CONCLUSION: Differences between patients mainly concerned educational level and area of residence with few differences regarding clinical profile. Differences between practices of GPs and psychiatrists appear to reflect more the organization of the French care system than the competence of providers