40 research outputs found

    Development of a UV miniaturised Fourier transform spectrometer (MicroFTS) for the detection of dissolved organic carbon in water

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    Within the UK and overseas, there are increasing scientific and water industry needs to acquire spatially and temporally intensive measurements of levels and molecular character of dissolved organic carbon (DOC) in the aquatic environment. The need is particularly acute in upland catchments that are often crucial for drinking water supply, and where DOC concentrations are high and have been increasing in recent years. Spectrometer-based systems currently on the market for this purpose are heavy, cumbersome, have a large power requirement, not sensitive in low light conditions, measure absorbance at single wavelengths, require frequent recalibration by trained operators and provide data based on hidden algorithms that limit interpretation of the resulting data. We have developed a new smaller, lighter, and self-calibrating instrument, combining novel miniaturisation of Fourier Transform Spectrometry, and a new scientifically peer-reviewed (and published) approach to assessing DOC concentrations in water. The portable sensor system uses a xenon flash lamp, where the light pulse is collimated and focused into one input of a bifurcated fibre dip probe. At the fibre tip, light is collimated and reflected in the water sample region over a total path length of 5mm. Shorter wavelengths (near the UV) are absorbed due to water containing DOC concentration. Light from the output end of the bifurcated fibre is collimated and coupled to the micro Fourier Transform Spectrometer. Within the interferometer, a broadband beam splitter and two concave mirrors are used to create an optical path difference between the beams. A UV sensitive detector is placed at the focus point of the generated interferogram. The interferogram is recorded and a Fourier Transform is applied to retrieve the spectral data. An absorbance of the DOC is measured and when a ratio is taken between the water sample containing DOC and DI water. Both detector and flash-lamp are triggered by an on-board dual wavefunction generator with a delay of 100us between the pulses. The instrument has its own portable power supply for powering the flash-lamp and pulse generator and has the capability and input for connecting with a solar panel for recharging when required

    Contrasting vulnerability of drained tropical and high-latitude peatlands to fluvial loss of stored carbon

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    Carbon sequestration and storage in peatlands rely on consistently highwater tables. Anthropogenic pressures including drainage, burning, land conversion for agriculture, timber, and biofuel production, cause loss of peat-forming vegetation and exposure of previously anaerobic peat to aerobic decomposition. This can shift peatlands from net CO2 sinks to large CO2 sources, releasing carbon held for millennia. Peatlands also export significant quantities of carbon via fluvial pathways, mainly as dissolved organic carbon (DOC). We analyzed radiocarbon (14C) levels of DOC in drainage water from multiple peatlands in Europe and Southeast Asia, to infer differences in the age of carbon lost from intact and drained systems. In most cases, drainage led to increased release of older carbon from the peat profile but withmarked differences related to peat type. Very low DOC-14C levels in runoff from drained tropical peatlands indicate loss of very old (centuries to millennia) stored peat carbon. High-latitude peatlands appear more resilient to drainage; 14C measurements from UK blanket bogs suggest that exported DOC remains young (500 year) carbon in high-latitude systems. Rewetting at least partially offsets drainage effects on DOC age

    Simulating long-term carbon nitrogen and phosphorus biogeochemical cycling in agricultural environments

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    Understanding how agricultural practices alter biogeochemical cycles is vital for maintaining land productivity, food security, and other ecosystem services such as carbon sequestration. However, these are complex, highly coupled long-term processes that are difficult to observe or explore through empirical science alone. Models are required that capture the main anthropogenic disturbances, whilst operating across regions and long timescales, simulating both natural and agricultural environments, and shifts among these. Many biogeochemical models neglect agriculture or interactions between carbon and nutrient cycles, which is surprising given the scale of intervention in nitrogen and phosphorus cycles introduced by agriculture. This gap is addressed here, using a plant-soil model that simulates integrated soil carbon, nitrogen and phosphorus (CNP) cycling across natural, semi-natural and agricultural environments. The model is rigorously tested both spatially and temporally using data from long-term agricultural experiments across temperate environments. The model proved capable of reproducing the magnitude of and trends in soil nutrient stocks, and yield responses to nutrient addition. The model has potential to simulate anthropogenic effects on biogeochemical cycles across northern Europe, for long timescales (centuries) without site-specific calibration, using easily accessible input data. The results demonstrate that weatherable P from parent material has a considerable effect on modern pools of soil C and N, despite significant perturbation of nutrient cycling from agricultural practices, highlighting the need to integrate both geological and agricultural processes to understand effects of land-use change on food security, C storage and nutrient sustainability. The results suggest that an important process or source of P is currently missing in our understanding of agricultural biogeochemical cycles. The model could not explain how yields were sustained in plots with low P fertiliser addition. We suggest that plant access to organic P is a key uncertainty warranting further research, particularly given sustainability concerns surrounding rock sources of P fertiliser

    Distinct and Shared Roles of β-Arrestin-1 and β-Arrestin-2 on the Regulation of C3a Receptor Signaling in Human Mast Cells

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    BACKGROUND: The complement component C3a induces degranulation in human mast cells via the activation of cell surface G protein coupled receptors (GPCR; C3aR). For most GPCRs, agonist-induced receptor phosphorylation leads to the recruitment of β-arrestin-1/β-arrestin-2; resulting in receptor desensitization and internalization. Activation of GPCRs also leads to ERK1/2 phosphorylation via two temporally distinct pathways; an early response that reflects G protein activation and a delayed response that is G protein independent but requires β-arrestins. The role of β-arrestins on C3aR activation/regulation in human mast cells, however, remains unknown. METHODOLOGY/PRINCIPAL FINDINGS: We utilized lentivirus short hairpin (sh)RNA to stably knockdown the expression of β-arrestin-1 and β-arrrestin-2 in human mast cell lines, HMC-1 and LAD2 that endogenously expresses C3aR. Silencing β-arrestin-2 attenuated C3aR desensitization, blocked agonist-induced receptor internalization and rendered the cells responsive to C3a for enhanced NF-κB activity as well as chemokine generation. By contrast, silencing β-arrestin-1 had no effect on these responses but resulted in a significant decrease in C3a-induced mast cell degranulation. In shRNA control cells, C3a caused a transient ERK1/2 phosphorylation, which peaked at 5 min but disappeared by 10 min. Knockdown of β-arrestin-1, β-arrestin-2 or both enhanced the early response to C3a and rendered the cells responsive for ERK1/2 phosphorylation at later time points (10-30 min). Treatment of cells with pertussis toxin almost completely blocked both early and delayed C3a-induced ERK1/2 phosphorylation in β-arrestin1/2 knockdown cells. CONCLUSION/SIGNIFICANCE: This study demonstrates distinct roles for β-arrestins-1 and β-arrestins-2 on C3aR desensitization, internalization, degranulation, NF-κB activation and chemokine generation in human mast cells. It also shows that both β-arrestin-1 and β-arrestin-2 play a novel and shared role in inhibiting G protein-dependent ERK1/2 phosphorylation. These findings reveal a new level of complexity for C3aR regulation by β-arrestins in human mast cells

    Soil phosphorus supply controls P nutrition strategies of beech forest ecosystems in Central Europe

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    A new era for understanding amyloid structures and disease

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    The aggregation of proteins into amyloid fibrils and their deposition into plaques and intracellular inclusions is the hallmark of amyloid disease. The accumulation and deposition of amyloid fibrils, collectively known as amyloidosis, is associated with many pathological conditions that can be associated with ageing, such as Alzheimer disease, Parkinson disease, type II diabetes and dialysis-related amyloidosis. However, elucidation of the atomic structure of amyloid fibrils formed from their intact protein precursors and how fibril formation relates to disease has remained elusive. Recent advances in structural biology techniques, including cryo-electron microscopy and solid-state NMR spectroscopy, have finally broken this impasse. The first near-atomic-resolution structures of amyloid fibrils formed in vitro, seeded from plaque material and analysed directly ex vivo are now available. The results reveal cross-β structures that are far more intricate than anticipated. Here, we describe these structures, highlighting their similarities and differences, and the basis for their toxicity. We discuss how amyloid structure may affect the ability of fibrils to spread to different sites in the cell and between organisms in a prion-like manner, along with their roles in disease. These molecular insights will aid in understanding the development and spread of amyloid diseases and are inspiring new strategies for therapeutic intervention

    Harmful Elements in Estuarine and Coastal Systems

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    Estuaries and coastal zones are dynamic transitional systems which provide many economic and ecological benefits to humans, but also are an ideal habitat for other organisms as well. These areas are becoming contaminated by various anthropogenic activities due to a quick economic growth and urbanization. This chapter explores the sources, chemical speciation, sediment accumulation and removal mechanisms of the harmful elements in estuarine and coastal seawaters. It also describes the effects of toxic elements on aquatic flora and fauna. Finally, the toxic element pollution of the Venice Lagoon, a transitional water body located in the northeastern part of Italy, is discussed as a case study, by presenting the procedures adopted to measure the extent of the pollution, the impacts on organisms and the restoration activities

    Critical loads of heavy metals for soils

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    To enable a precautionary risk assessment for future inputs of metals, steady-state methods have been developed to assess critical loads of metals avoiding long-term risks to food uality and eco-toxicological effects on organisms in soils and surface waters. A critical load for metals equals the load resulting at steady state in a concentration in a compartment (e.g. soil solution, plant, fish) that equals the critical limit for that compartment. This chapter presents an overview of methods to assess critical limits and critical loads of metals, with a focus on cadmium (Cd), lead (Pb), copper (Cu) and zinc (Zn) in soils in relation to impacts on: (i) agriculture (food quality and crop health) and (ii) ecology (plants, invertebrates and soil organisms invloved in nutrient cycling processes). Results are presented using generic input data. Furthermore, examples of national and European applications are shown. Results are discussed in view of the uncertainty and applicability of the critical load concept for heavy metals in future agreements on the reduction of metal emissions. It is concluded that for policy applications, dynamic models are also needed to estimate the times involved in attaining a certain chemical state in response to input (deposition, fertilisers or manure) scenarios
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