A clinopyroxene record of primitive melt diversity and mantle heterogeneity beneath Italy

The young potassium-rich volcanic rocks of peninsular Italy are the products of a complex post-collisional geodynamic setting. These volcanic rocks exhibit extreme compositional variability in space and time, resulting from large variations in the subducted material in their mantle sources. The genetic relationships between distinct Italian magmatic series—shoshonitic, potassic, ultrapotassic and lamproitic, among others—that are closely related in space and time, as well as the exact nature and provenance of the metasomatic agents, are subject to active debate. The earliest crystallised silicate phases from mafic lavas—olivine and clinopyroxene—carry valuable information on the nature of mantle sources and melt extraction processes. Because Mg-rich clinopyroxene incorporates significant amounts of incompatible elements and is a ubiquitous phase in mafic Italian lavas, it potentially represents a versatile instrument for delineating the compositional complexity and regional variability of subduction-modified mantle sources in this region. Here we present the results of an extensive study of Mg-rich clinopyroxene (Mg# = 88–93 mol%) from potassium-rich mafic rocks from a chain of volcanic centres in central-southern Italy, from Tuscany down to Campania. We compare major- and trace-element data from clinopyroxenes with those from bulk rocks and olivine-hosted melt inclusions, using new estimates of trace-element partitioning between clinopyroxene and potassium-rich magmas based on cogenetic clinopyroxene-olivine crystallisation. The Mg-rich clinopyroxenes show a marked compositional diversity that reflects the nature of the (near-)primary mantle-derived melts from which they crystallised, and allow us to characterise the metasomatic agents responsible for the formation of different compositional end-members. We demonstrate that clinopyroxenes provide a detailed archive of mantle heterogeneity beneath Italy, highlighting systematic variations both regionally and beneath individual volcanic complexes

Perturbed Rotations of a Rigid Body Close to the Lagrange Case under the Action of Unsteady Perturbation Torques

Perturbed rotations of a rigid body close to the Lagrange case under the action of perturbation torques slowly varying in time are investigated. Conditions are presented for the possibility of averaging the equations of motion with respect to the nutation angle and the averaged system of equations of motion is obtained. In the case of the rotational motion of the body in the linear-dissipative medium the numerical integration of the averaged system of equations is conducted

The South Armenian Block: Gondwanan origin and Tethyan evolution in space and time

The geodynamic evolution of the South Armenian Block (SAB) within the Tethyan realm during the Palaeozoic to present-day is poorly constrained. Much of the SAB is covered by Cenozoic sediments so that the relationships between the SAB and the neighbouring terranes of Central Iran, the Pontides and Taurides are unclear. Here we present new geochronological, palaeomagnetic, and geochemical constraints to shed light on the Gondwanan and Cimmerian provenance of the SAB, timing of its rifting, and geodynamic evolution since the Permian. We report new 40Ar/39Ar and zircon U-Pb ages and compositional data on magmatic sills and dykes in the Late Devonian sedimentary cover, as well as metamorphic rocks that constitute part of the SAB basement. Zircon age distributions, ranging from ∼3.6 Ga to 100 Ma, firmly establish a Gondwanan origin for the SAB. Trondhjemite intrusions into the basement at ∼263 Ma are consistent with a SW-dipping active continental margin. Mafic intraplate intrusions at ∼246 Ma (OIB) and ∼234 Ma (P-MORB) in the sedimentary cover likely represent the incipient stages of breakup of the NE Gondwanan margin and opening of the Neotethys. Andesitic dykes at ∼117 Ma testify to the melting of subduction-modified lithosphere. In contrast to current interpretations, we show that the SAB should be considered separate from the Taurides, and that the Armenian ophiolite complexes formed chiefly in the Eurasian forearc. Based on the new constraints, we provide a geodynamic reconstruction of the SAB since the Permian, in which it started rifting from Gondwana alongside the Pontides, likely reached the Iranian margin in Early Jurassic times, and was subject to episodes of intraplate (∼189 Ma) and NE-dipping subduction-related (∼117 Ma) magmatism

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

J. Kaprio, A. Palotie, A. Raevuori-Helkamaa ja S. Ripatti ovat työryhmän Eating Disorders Working Group of the Psychiatric Genomics Consortium jäseniä. Erratum in: Sci Rep. 2017 Aug 21;7(1):8379, doi: 10.1038/s41598-017-06409-3We conducted a genome-wide association study (GWAS) of anorexia nervosa (AN) using a stringently defined phenotype. Analysis of phenotypic variability led to the identification of a specific genetic risk factor that approached genome-wide significance (rs929626 in EBF1 (Early B-Cell Factor 1); P = 2.04 x 10(-7); OR = 0.7; 95% confidence interval (CI) = 0.61-0.8) with independent replication (P = 0.04), suggesting a variant-mediated dysregulation of leptin signaling may play a role in AN. Multiple SNPs in LD with the variant support the nominal association. This demonstrates that although the clinical and etiologic heterogeneity of AN is universally recognized, further careful sub-typing of cases may provide more precise genomic signals. In this study, through a refinement of the phenotype spectrum of AN, we present a replicable GWAS signal that is nominally associated with AN, highlighting a potentially important candidate locus for further investigation.Peer reviewe

Common Genetic Variation And Age at Onset Of Anorexia Nervosa

Background Genetics and biology may influence the age at onset of anorexia nervosa (AN). The aims of this study were to determine whether common genetic variation contributes to AN age at onset and to investigate the genetic associations between age at onset of AN and age at menarche. Methods A secondary analysis of the Psychiatric Genomics Consortium genome-wide association study (GWAS) of AN was performed which included 9,335 cases and 31,981 screened controls, all from European ancestries. We conducted GWASs of age at onset, early-onset AN (< 13 years), and typical-onset AN, and genetic correlation, genetic risk score, and Mendelian randomization analyses. Results Two loci were genome-wide significant in the typical-onset AN GWAS. Heritability estimates (SNP-h2) were 0.01-0.04 for age at onset, 0.16-0.25 for early-onset AN, and 0.17-0.25 for typical-onset AN. Early- and typical-onset AN showed distinct genetic correlation patterns with putative risk factors for AN. Specifically, early-onset AN was significantly genetically correlated with younger age at menarche, and typical-onset AN was significantly negatively genetically correlated with anthropometric traits. Genetic risk scores for age at onset and early-onset AN estimated from independent GWASs significantly predicted age at onset. Mendelian randomization analysis suggested a causal link between younger age at menarche and early-onset AN. Conclusions Our results provide evidence consistent with a common variant genetic basis for age at onset and implicate biological pathways regulating menarche and reproduction.Peer reviewe

Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

Genetic influences on psychiatric disorders transcend diagnostic boundaries, suggesting substantial pleiotropy of contributing loci. However, the nature and mechanisms of these pleiotropic effects remain unclear. We performed analyses of 232,964 cases and 494,162 controls from genome-wide studies of anorexia nervosa, attention-deficit/hyper-activity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, and Tourette syndrome. Genetic correlation analyses revealed a meaningful structure within the eight disorders, identifying three groups of inter-related disorders. Meta-analysis across these eight disorders detected 109 loci associated with at least two psychiatric disorders, including 23 loci with pleiotropic effects on four or more disorders and 11 loci with antagonistic effects on multiple disorders. The pleiotropic loci are located within genes that show heightened expression in the brain throughout the lifespan, beginning prenatally in the second trimester, and play prominent roles in neurodevelopmental processes. These findings have important implications for psychiatric nosology, drug development, and risk prediction.Peer reviewe

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

Background Suicide is a leading cause of death worldwide, and nonfatal suicide attempts, which occur far more frequently, are a major source of disability and social and economic burden. Both have substantial genetic etiology, which is partially shared and partially distinct from that of related psychiatric disorders. Methods We conducted a genome-wide association study (GWAS) of 29,782 suicide attempt (SA) cases and 519,961 controls in the International Suicide Genetics Consortium (ISGC). The GWAS of SA was conditioned on psychiatric disorders using GWAS summary statistics via multitrait-based conditional and joint analysis, to remove genetic effects on SA mediated by psychiatric disorders. We investigated the shared and divergent genetic architectures of SA, psychiatric disorders, and other known risk factors. Results Two loci reached genome-wide significance for SA: the major histocompatibility complex and an intergenic locus on chromosome 7, the latter of which remained associated with SA after conditioning on psychiatric disorders and replicated in an independent cohort from the Million Veteran Program. This locus has been implicated in risk-taking behavior, smoking, and insomnia. SA showed strong genetic correlation with psychiatric disorders, particularly major depression, and also with smoking, pain, risk-taking behavior, sleep disturbances, lower educational attainment, reproductive traits, lower socioeconomic status, and poorer general health. After conditioning on psychiatric disorders, the genetic correlations between SA and psychiatric disorders decreased, whereas those with nonpsychiatric traits remained largely unchanged. Conclusions Our results identify a risk locus that contributes more strongly to SA than other phenotypes and suggest a shared underlying biology between SA and known risk factors that is not mediated by psychiatric disorders.Peer reviewe

Shared genetic risk between eating disorder- and substance-use-related phenotypes:Evidence from genome-wide association studies

First published: 16 February 202