65 research outputs found

    The sedimentary imprint of Pleistocene glacio-eustasy: Implications for global correlations of seismic sequences

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    We evaluate lithofacies, chronology, and seismic sequences from the Canterbury Basin, New Zealand passive continental slope (Integrated Ocean Drilling Program [IODP] Expedition 317 Site U1352 and environs) and compare this with slope sequences from the New Jersey passive margin. Our goal is to understand continental slope sedimentation in response to glacio-eustasy and test the concepts of sequence stratigraphy. High-resolution geochemical elemental and lithostratigraphic analyses were calibrated to a chronology constructed from benthic foramininferal oxygen isotopes for the past ~1.8 m.y. We identify lithofacies successions by their unique geochemical and lithologic signature and correlate them with marine isotope stages (MIS) at Milankovitch 100 k.y. (MIS 1ā€“12) and 41 k.y. (MIS 13ā€“63) periods. Eight seismic sequence boundaries (U13ā€“U19) were identified from high-resolution multichannel seismic data, providing a seismic stratigraphic framework. Except for MIS 1ā€“5 and MIS 54ā€“55, there are 2ā€“16 MIS stages and a comparable number of lithofacies contained within each seismic sequence, indicating that it took one to several glacio-eustatic cycles to build each seismic stratigraphic sequence. These findings support prior results obtained by the Ocean Drilling Program (ODP) Leg 174A on the New Jersey continental slope. On both margins, there is a strong correlation between seismic sequences, lithofacies, and MIS, thus linking them to glacio-eustasy. However, the correlation between MIS and seismic sequences is not one-to-one, and Pleistocene seismic sequences on the two margins are not synchronous. Local conditions, including differences in sedimentation rates and creation of accommodation space, strongly influenced sediment preservation at each location, revealing that high-frequency Pleistocene seismic sequences need not correlate globally

    Indonesian Throughflow drove Australian climate from humid Pliocene to arid Pleistocene

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    Late Miocene to mid-Pleistocene sedimentary proxy records reveal that northwest Australia underwent an abrupt transition from dry to humid climate conditions at 5.5 million years (Ma), likely receiving year-round rainfall, but after ~3.3 Ma, climate shifted toward an increasingly seasonal precipitation regime. The progressive constriction of the Indonesian Throughflow likely decreased continental humidity and transferred control of northwest Australian climate from the Pacific to the Indian Ocean, leading to drier conditions punctuated by monsoonal precipitation. The northwest dust pathway and fully established seasonal and orbitally controlled precipitation were in place by ~2.4 Ma, well after the intensification of Northern Hemisphere glaciation. The transition from humid to arid conditions was driven by changes in Pacific and Indian Ocean circulation and regional atmospheric moisture transport, influenced by the emerging Maritime Continent. We conclude that the Maritime Continent is the switchboard modulating teleconnections between tropical and high-latitude climate systems

    Development of an improved blood-stage malaria vaccine targeting the essential RH5-CyRPA-RIPR invasion complex

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    Reticulocyte-binding protein homologue 5 (RH5), a leading blood-stage Plasmodium falciparum malaria vaccine target, interacts with cysteine-rich protective antigen (CyRPA) and RH5-interacting protein (RIPR) to form an essential heterotrimeric ā€œRCR-complexā€. We investigate whether RCR-complex vaccination can improve upon RH5 alone. Using monoclonal antibodies (mAbs) we show that parasite growth-inhibitory epitopes on each antigen are surface-exposed on the RCR-complex and that mAb pairs targeting different antigens can function additively or synergistically. However, immunisation of female rats with the RCR-complex fails to outperform RH5 alone due to immuno-dominance of RIPR coupled with inferior potency of anti-RIPR polyclonal IgG. We identify that all growth-inhibitory antibody epitopes of RIPR cluster within the C-terminal EGF-like domains and that a fusion of these domains to CyRPA, called ā€œR78Cā€, combined with RH5, improves the level of in vitro parasite growth inhibition compared to RH5 alone. These preclinical data justify the advancement of the RH5.1 + R78C/Matrix-Mā„¢ vaccine candidate to Phase 1 clinical trial

    Evidence for widespread creep on the flanks of the Sea of Marmara transform basin from marine geophysical data

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    "Wave" fields have long been recognized in marine sediments on the flanks of basins and oceans in both tectonically active and inactive environments. The origin of "waves" (hereafter called undulations) is controversial; competing models ascribe them to depositional processes, gravity-driven downslope creep or collapse, and/or tectonic shortening. Here we analyze pervasive undulation fields identified in swath bathymetry and new high-resolution multichannel seismic (MCS) reflection data from the Sea of Marmara, Turkey. Although they exhibit some of the classical features of sediment waves, the following distinctive characteristics exclude a purely depositional origin: (1) parallelism between the crests of the undulations and bathymetric contours over a wide range of orientations, (2) steep flanks of the undulations (up to Ć¢Ė†Ā¼40Ā°), and (3) increases in undulations amplitude with depth. We argue that the undulations are folds formed by gravity-driven downslope creep that have been augmented by depositional processes. These creep folds develop over long time periods (ā‰„0.5 m.y.) and stand in contrast to geologically instantaneous collapse. Stratigraphic growth on the upslope limbs indicates that deposition contributes to the formation and upslope migration of the folds. The temporal and spatial evolution of the creep folds is clearly related to rapid tilting in this tectonically active transform basin

    Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos

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    Prior GWAS have identified loci associated with red blood cell (RBC) traits in populations of European, African, and Asian ancestry. These studies have not included individuals with an Amerindian ancestral background, such as Hispanics/Latinos, nor evaluated the full spectrum of genomic variation beyond single nucleotide variants. Using a custom genotyping array enriched for Amerindian ancestral content and 1000 Genomes imputation, we performed GWAS in 12,502 participants of Hispanic Community Health Study and Study of Latinos (HCHS/SOL) for hematocrit, hemoglobin, RBC count, RBC distribution width (RDW), and RBC indices. Approximately 60% of previously reported RBC trait loci generalized to HCHS/SOL Hispanics/Latinos, including African ancestral alpha- and beta-globin gene variants. In addition to the known 3.8kb alpha-globin copy number variant, we identified an Amerindian ancestral association in an alpha-globin regulatory region on chromosome 16p13.3 for mean corpuscular volume and mean corpuscular hemoglobin. We also discovered and replicated three genome-wide significant variants in previously unreported loci for RDW (SLC12A2 rs17764730, PSMB5 rs941718), and hematocrit (PROX1 rs3754140). Among the proxy variants at the SLC12A2 locus we identified rs3812049, located in a bi-directional promoter between SLC12A2 (which encodes a red cell membrane ion-transport protein) and an upstream anti-sense long-noncoding RNA, LINC01184, as the likely causal variant. We further demonstrate that disruption of the regulatory element harboring rs3812049 affects transcription of SLC12A2 and LINC01184 in human erythroid progenitor cells. Together, these results reinforce the importance of genetic study of diverse ancestral populations, in particular Hispanics/Latinos
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