69 research outputs found

    Bomb-<sup>14</sup>C analysis of ecosystem respiration reveals that peatland vegetation facilitates release of old carbon

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    The largest terrestrial-to-atmosphere carbon flux is respired CO&lt;sub&gt;2&lt;/sub&gt;. However, the partitioning of soil and plant sources, understanding of contributory mechanisms, and their response to climate change are uncertain. A plant removal experiment was established within a peatland located in the UK uplands to quantify respiration derived from recently fixed plant carbon and that derived from decomposition of soil organic matter, using natural abundance &lt;sup&gt;13&lt;/sup&gt;C and bomb-&lt;sup&gt;14&lt;/sup&gt;C as tracers. Soil and plant respiration sources were found respectively to contribute ~ 36% and between 41-54% of the total ecosystem CO&lt;sub&gt;2&lt;/sub&gt; flux. Respired CO&lt;sub&gt;2&lt;/sub&gt; produced in the clipped (‘soil’) plots had a mean age of ~ 15 years since fixation from the atmosphere, whereas the &lt;sup&gt;14&lt;/sup&gt;C content of ecosystem CO&lt;sub&gt;2&lt;/sub&gt; was statistically indistinguishable from the contemporary atmosphere. Results of carbon mass balance modelling showed that, in addition to respiration from bulk soil and plant respired CO&lt;sub&gt;2&lt;/sub&gt;, a third, much older source of CO&lt;sub&gt;2&lt;/sub&gt; existed. This source, which we suggest is CO&lt;sub&gt;2&lt;/sub&gt; derived from the catotelm constituted between ~ 10 and 23% of total ecosystem respiration and had a mean radiocarbon age of between several hundred to ~ 2000 years before present (BP). These findings show that plant-mediated transport of CO&lt;sub&gt;2&lt;/sub&gt; produced in the catotelm may form a considerable component of peatland ecosystem respiration. The implication of this discovery is that current assumptions in terrestrial carbon models need to be re-evaluated to consider the climate sensitivity of this third source of peatland CO&lt;sub&gt;2&lt;/sub&gt;

    Transcriptome-wide association study of blood cell traits in african ancestry and hispanic/latino populations

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    Background: Thousands of genetic variants have been associated with hematological traits, though target genes remain unknown at most loci. Moreover, limited analyses have been conducted in African ancestry and Hispanic/Latino populations; hematological trait associated variants more common in these populations have likely been missed. Methods: To derive gene expression prediction models, we used ancestry-stratified datasets from the Multi-Ethnic Study of Atherosclerosis (MESA, including n = 229 African American and n = 381 Hispanic/Latino participants, monocytes) and the Depression Genes and Networks study (DGN, n = 922 European ancestry participants, whole blood). We then performed a transcriptome-wide association study (TWAS) for platelet count, hemoglobin, hematocrit, and white blood cell count in African (n = 27,955) and Hispanic/Latino (n = 28,324) ancestry participants. Results: Our results revealed 24 suggestive signals (p &lt; 1 × 10−4 ) that were conditionally distinct from known GWAS identified variants and successfully replicated these signals in European ancestry subjects from UK Biobank. We found modestly improved correlation of predicted and measured gene expression in an independent African American cohort (the Genetic Epidemiology Network of Arteriopathy (GENOA) study (n = 802), lymphoblastoid cell lines) using the larger DGN reference panel; however, some genes were well predicted using MESA but not DGN. Conclusions: These analyses demonstrate the importance of performing TWAS and other genetic analyses across diverse populations and of balancing sample size and ancestry background matching when selecting a TWAS reference panel

    Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches

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    Extracellular vesicles (EVs), through their complex cargo, can reflect the state of their cell of origin and change the functions and phenotypes of other cells. These features indicate strong biomarker and therapeutic potential and have generated broad interest, as evidenced by the steady year-on-year increase in the numbers of scientific publications about EVs. Important advances have been made in EV metrology and in understanding and applying EV biology. However, hurdles remain to realising the potential of EVs in domains ranging from basic biology to clinical applications due to challenges in EV nomenclature, separation from non-vesicular extracellular particles, characterisation and functional studies. To address the challenges and opportunities in this rapidly evolving field, the International Society for Extracellular Vesicles (ISEV) updates its ‘Minimal Information for Studies of Extracellular Vesicles’, which was first published in 2014 and then in 2018 as MISEV2014 and MISEV2018, respectively. The goal of the current document, MISEV2023, is to provide researchers with an updated snapshot of available approaches and their advantages and limitations for production, separation and characterisation of EVs from multiple sources, including cell culture, body fluids and solid tissues. In addition to presenting the latest state of the art in basic principles of EV research, this document also covers advanced techniques and approaches that are currently expanding the boundaries of the field. MISEV2023 also includes new sections on EV release and uptake and a brief discussion of in vivo approaches to study EVs. Compiling feedback from ISEV expert task forces and more than 1000 researchers, this document conveys the current state of EV research to facilitate robust scientific discoveries and move the field forward even more rapidly

    Whole-genome sequencing reveals host factors underlying critical COVID-19

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    Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease

    Three representative UK moorland soils show differences in decadal release of dissolved organic carbon in response to environmental change

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    Moorland carbon reserves in organo-mineral soils may be crucial to predicting landscape-scale variability in soil carbon losses, an important component of which is dissolved organic carbon (DOC). Surface water DOC trends are subject to a range of scaling, transport and biotic processes that disconnect them from signals in the catchment's soils. Long-term soil datasets are vital to identify changes in DOC release at source and soil C depletion. Here we show, that moorland soil solution DOC concentrations at three key UK Environmental Change Network sites increased between 1993-2007 in both surface-and sub-soil of a freely-draining Podzol (48% and 215% increases in O and Bs horizons, respectively), declined in a gleyed Podzol and showed no change in a Peat. Our principal findings were that: (1) considerable heterogeneity in DOC response appears to exist between different soils that is not apparent from the more consistent observed trends for streamwaters, and (2) freely-draining organo-mineral Podzol showed increasing DOC concentrations, countering the current scientific focus on soil C destabilization in peats. We discuss how the key solubility controls on DOC associated with coupled physico-chemical factors of ionic strength, acid deposition recovery, soil hydrology and temperature cannot readily be separated. Yet, despite evidence that all sites are recovering from acidification the soil-specific responses to environmental change have caused divergence in soil DOC concentration trends. The study shows that the properties of soils govern their specific response to an approximately common set of broad environmental drivers. Key soil properties are indicated to be drainage, sulphate and DOC sorption capacity. Soil properties need representation in process-models to understand and predict the role of soils in catchment to global C budgets. Catchment hydrological (i.e. transport) controls may, at present, be governing the more ubiquitous rises in river DOC concentration trends, but soil (i.e. source) controls provide the key to prediction of future C loss to waters and the atmosphere

    Mercury in rivers in NW England: from rural headwaters to the heartlands of the historic industrial base

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    Total mercury (T-Hg) concentrations in rivers are described across a rural to urban/industrial and agricultural landscape gradient in NW England. T-Hg ranges between 0.2 and 230 ng L-1. The regional median was 3.6 ng L-1 with individual river medians ranging between 1.9 and 8.3 ng L-1. Median T-Hg concentrations were sometimes moderately higher for the lowland areas and at higher flows. Our estimates suggest that the Ribble estuary receives 9.2 kg yr-1 and the Wyre estuary 0.7 kg yr-1. In order to examine regional inputs from urban/industrial components, regression analysis was undertaken by comparing three types of hydrochemical signature: suspended sediments (SS), which provides a measure of the particulate component, dissolved organic carbon (DOC), that provides an indication of humic/fulvic acids that are part of the organic colloids and strong chelating agents, and boron a marker of sewage effluents and population density. The results show high positive relationships of T-Hg with both SS and DOC, but no relationship with the urban/industrial signal. The regression analysis with T-Hg indicated on average a gradient of 0.33 ng mg-1 for DOC and 0.2 ng mg-1 for SS. They indicate the primary importance of a diffuse source of T-Hg. For the upland areas and cleaner river systems, the linkages between T-Hg and DOC were particularly strong, while for the lowland areas, the linkage with SS proved stronger. Analysis of a later subset of data that partitions the SS into organic and inorganic fractions indicated that the T-Hg was primarily linked with the organic fraction. Indeed, multiple regression of T-Hg with DOC and POM reveal gradients similar to other parts of the Worl
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