17 research outputs found

    Tectonic history of the Kyrgyz South Tien Shan (Atbashi-Inylchek) suture zone : the role of inherited structures during deformation-propagation

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    Multimethod chronology was applied on intrusives bordering the Kyrgyz South Tien Shan suture (STSs) to decipher the timing of (1) formation and amalgamation of the suturing units and (2) intracontinental deformation that built the bordering mountain ranges. Zircon U/Pb data indicate similarities between the Tien Shan and Tarim Precambrian crust. Caledonian (similar to 440-410 Ma) and Hercynian (similar to 310-280 Ma) zircon U/Pb ages were found at the edge of the STSs, related to subduction and closure of the Turkestan Ocean and the formation of the suture itself. Permian-Triassic (similar to 280-210 Ma) titanite fission track and zircon (U-Th)/He data record the first signs of exhumation when the STSs evolved into a shear zone and the adjacent Tarim basin started to subside. Low-temperature thermochronological (apatite fission track, zircon and apatite (U-Th)/He) analyses reveal three distinct cooling phases, becoming younger toward the STSs center: (1) Jurassic-Cretaceous cooling ages provide evidence that a Mesozoic South Tien Shan orogen formed as a response to the Cimmerian orogeny; (2) Early Paleogene (similar to 60-45 Ma) data indicate a renewed pulse of STSs reactivation during the Early Cenozoic; (3) Neogene ages constrain the onset of the modern Tien Shan mountain building to the Late Oligocene (similar to 30-25 Ma), which intensified during the Miocene (similar to 10-8 Ma) and Pliocene (similar to 3-2 Ma). The Cenozoic signals may reflect renewed responses to collisions at the southern Eurasian border (i.e., the Kohistan-Dras and India-Eurasia collisions). This progressive rejuvenation of the STSs demonstrates that deformation has not migrated steadily into the forelands, but was focused on pre-existing basement structures

    Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa

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    In MRI scans of patients with anorexia nervosa (AN), reductions in brain volume are often apparent. However, it is unknown whether such brain abnormalities are influenced by genetic determinants that partially overlap with those underlying AN. Here, we used a battery of methods (LD score regression, genetic risk scores, sign test, SNP effect concordance analysis, and Mendelian randomization) to investigate the genetic covariation between subcortical brain volumes and risk for AN based on summary measures retrieved from genome-wide association studies of regional brain volumes (ENIGMA consortium, n = 13,170) and genetic risk for AN (PGC-ED consortium, n = 14,477). Genetic correlations ranged from − 0.10 to 0.23 (all p > 0.05). There were some signs of an inverse concordance between greater thalamus volume and risk for AN (permuted p = 0.009, 95% CI: [0.005, 0.017]). A genetic variant in the vicinity of ZW10, a gene involved in cell division, and neurotransmitter and immune system relevant genes, in particular DRD2, was significantly associated with AN only after conditioning on its association with caudate volume (pFDR = 0.025). Another genetic variant linked to LRRC4C, important in axonal and synaptic development, reached significance after conditioning on hippocampal volume (pFDR = 0.021). In this comprehensive set of analyses and based on the largest available sample sizes to date, there was weak evidence for associations between risk for AN and risk for abnormal subcortical brain volumes at a global level (that is, common variant genetic architecture), but suggestive evidence for effects of single genetic markers. Highly powered multimodal brain- and disorder-related genome-wide studies are needed to further dissect the shared genetic influences on brain structure and risk for AN
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