8 research outputs found

    Spatial and temporal patterns in petrogenic organic carbon mobilisation during the Paleocene-Eocene Thermal Maximum

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    The Paleocene‐Eocene Thermal Maximum (PETM) was a transient global warming event and is recognized in the geologic record by a prolonged negative carbon isotope excursion (CIE). The onset of the CIE was due to a rapid influx of 13C‐depleted carbon into the ocean‐atmosphere system. However, the mechanisms required to sustain the negative CIE remains unclear. Enhanced mobilization and oxidation of petrogenic organic carbon (OCpetro) has been invoked to explain elevated atmospheric carbon dioxide concentrations after the onset of the CIE. However, existing evidence is limited to the mid‐latitudes and subtropics. Here, we determine whether: (a) enhanced mobilization and subsequent burial of OCpetro in marine sediments was a global phenomenon; and (b) whether it occurred throughout the PETM. To achieve this, we utilize a lipid biomarker approach to trace and quantify OCpetro burial in a global compilation of PETM‐aged shallow marine sites (n = 7, including five new sites). Our results confirm that OCpetro mass accumulation rates (MARs) increased within the subtropics and mid‐latitudes during the PETM, consistent with evidence of higher physical erosion rates and intense episodic rainfall events. High‐latitude sites do not exhibit drastic changes in the source of organic carbon during the PETM and OCpetro MARs increase slightly or remain stable, perhaps due a more stable hydrological regime. Crucially, we also demonstrate that OCpetro MARs remained elevated during the recovery phase of the PETM. Although OCpetro oxidation was likely an important positive feedback mechanism throughout the PETM, we show that this feedback was both spatially and temporally variable

    A global in vivo Drosophila RNAi screen identifies NOT3 as a conserved regulator of heart function.

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    Heart diseases are the most common causes of morbidity and death in humans. Using cardiac-specific RNAi-silencing in Drosophila, we knocked down 7061 evolutionarily conserved genes under conditions of stress. We present a first global roadmap of pathways potentially playing conserved roles in the cardiovascular system. One critical pathway identified was the CCR4-Not complex implicated in transcriptional and posttranscriptional regulatory mechanisms. Silencing of CCR4-Not components in adult Drosophila resulted in myofibrillar disarray and dilated cardiomyopathy. Heterozygous not3 knockout mice showed spontaneous impairment of cardiac contractility and increased susceptibility to heart failure. These heart defects were reversed via inhibition of HDACs, suggesting a mechanistic link to epigenetic chromatin remodeling. In humans, we show that a common NOT3 SNP correlates with altered cardiac QT intervals, a known cause of potentially lethal ventricular tachyarrhythmias. Thus, our functional genome-wide screen in Drosophila can identify candidates that directly translate into conserved mammalian genes involved in heart function
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