2,832 research outputs found

    Melting mud in Earth's mantle

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    Melting of subducted sediment remains controversial, as direct observation of sediment melt generation at mantle depths is not possible. Geochemical fingerprints provide indirect evidence for subduction delivery of sediment to the mantle; however, sediment abundance in mantle-derived melt is generally low (0%ā€“2%), and difficult to detect. Here we provide evidence for melting of subducted sediment in granite sampled from an exhumed mantle section. Peraluminous granite dikes that intrude peridotite in the Omanā€“United Arab Emirates ophiolite have U-Pb ages of 99.8 Ā± 3.3 Ma that predate obduction. The dikes have unusually high oxygen isotope (Ī“18O) values for whole rock (14ā€“23ā€°) and quartz (20ā€“22ā€°), and yield the highest Ī“18O zircon values known (14ā€“28ā€°; values relative to Vienna standard mean ocean water [VSMOW]). The extremely high oxygen isotope ratios uniquely identify the melt source as high-Ī“18O marine sediment (pelitic and/or siliciceous mud), as no other source could produce granite with such anomalously high Ī“18O. Formation of high-Ī“18O sediment-derived (S-type) granite within peridotite requires subduction of sediment to the mantle, where it melted and intruded overlying mantle wedge. The granite suite described here contains the highest oxygen isotope ratios reported for igneous rocks, yet intruded mantle peridotite below the Mohorovičić seismic discontinuity, the most primitive oxygen isotope reservoir in the silicate Earth. Identifying the presence and quantifying the extent of sediment melting within the mantle has important implications for understanding subduction recycling of supracrustal material and effects on mantle heterogeneity over time.National Geographi

    Shubnikov-de Haas quantum oscillations reveal a reconstructed Fermi surface near optimal doping in a thin film of the cuprate superconductor Pr1.86Ce0.14CuO4Ā±Ī“

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    We study magnetotransport properties of the electron-doped superconductor Pr2-xCexCuO4Ā±Ī“ with x=0.14 in magnetic fields up to 92 T, and observe Shubnikov-de Haas magnetic quantum oscillations. The oscillations display a single frequency F=255Ā±10 T, indicating a small Fermi pocket that is āˆ¼1% of the two-dimensional Brillouin zone and consistent with a Fermi surface reconstructed from the large holelike cylinder predicted for these layered materials. Despite the low nominal doping, all electronic properties including the effective mass and Hall effect are consistent with overdoped compounds. Our study demonstrates that the exceptional chemical control afforded by high quality thin films will enable Fermi surface studies deep into the overdoped cuprate phase diagram

    The Rho family GEF FARP2 is activated by aPKC iota to control tight junction formation and polarity

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    The elaboration of polarity is central to organismal development and to the maintenance of functional epithelia. Among the controls determining polarity are the PAR proteins, PAR6, aPKCĪ¹ and PAR3, regulating both known and unknown effectors. Here, we identify FARP2 as a ā€˜RIPRā€™ motif-dependent partner and substrate of aPKCĪ¹ that is required for efficient polarisation and junction formation. Binding is conferred by a FERM/FA domainā€“kinase domain interaction and detachment promoted by aPKCĪ¹-dependent phosphorylation. FARP2 is shown to promote GTP loading of Cdc42, which is consistent with it being involved in upstream regulation of the polarising PAR6ā€“aPKCĪ¹ complex. However, we show that aPKCĪ¹ acts to promote the localised activity of FARP2 through phosphorylation. We conclude that this aPKCĪ¹āˆ’FARP2 complex formation acts as a positive feedback control to drive polarisation through aPKCĪ¹ and other Cdc42 effectors

    aPKC Inhibition by Par3 CR3 Flanking Regions Controls Substrate Access and Underpins Apical-Junctional Polarization

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    Atypical protein kinase C (aPKC) is a key apical-basal polarity determinant and Par complex component. It is recruited by Par3/Baz (Bazooka in Drosophila) into epithelial apical domains through high-affinity interaction. Paradoxically, aPKC also phosphorylates Par3/Baz, provoking its relocalization to adherens junctions (AJs). We show that Par3 conserved region 3 (CR3) forms a tight inhibitory complex with a primed aPKC kinase domain, blocking substrate access. A CR3 motif flanking its PKC consensus site disrupts the aPKC kinase N lobe, separating P-loop/Ī±B/Ī±C contacts. A second CR3 motif provides a high-affinity anchor. Mutation of either motif switches CR3 to an efficient in vitro substrate by exposing its phospho-acceptor site. In vivo, mutation of either CR3 motif alters Par3/Baz localization from apical to AJs. Our results reveal how Par3/Baz CR3 can antagonize aPKC in stable apical Par complexes and suggests that modulation of CR3 inhibitory arms or opposing aPKC pockets would perturb the interaction, promoting Par3/Baz phosphorylation

    Comparative Population Genetics of the Immunity Gene, Relish: Is Adaptive Evolution Idiosyncratic?

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    The frequency of adaptive evolution acting on common loci in distant lineages remains an outstanding question in evolutionary biology. We asked whether the immunity factor, Relish, a gene with a history of directional selection in Drosophila simulans, shows evidence of a similar selective history in other Drosophila species. We found only weak evidence of recurrent adaptive protein evolution at the Relish locus in three sister species pairs, suggesting that this key component of the insect immune system has an idiosyncratic evolutionary history in Drosophila
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