Distributed hydrological modelling of total dissolved phosphorus transport in an agricultural landscape, part I: distributed runoff generation

International audienceSuccessful implementation of best management practices for reducing non-point source (NPS) pollution requires knowledge of the location of saturated areas that produce runoff. A physically-based, fully-distributed, GIS-integrated model, the Soil Moisture Distribution and Routing (SMDR) model was developed to simulate the hydrologic behavior of small rural upland watersheds with shallow soils and steep to moderate slopes. The model assumes that gravity is the only driving force of water and that most overland flow occurs as saturation excess. The model uses available soil and climatic data, and requires little calibration. The SMDR model was used to simulate runoff production on a 164-ha farm watershed in Delaware County, New York, in the headwaters of New York City water supply. Apart from land use, distributed input parameters were derived from readily available data. Simulated hydrographs compared reasonably with observed flows at the watershed outlet over a eight year simulation period, and peak timing and intensities were well reproduced. Using off-site weather input data produced occasional missed event peaks. Simulated soil moisture distribution agreed well with observed hydrological features and followed the same spatial trend as observed soil moisture contents sampled on four transects. Model accuracy improved when input variables were calibrated within the range of SSURGO-available parameters. The model will be a useful planning tool for reducing NPS pollution from farms in landscapes similar to the Northeastern US

Distributed hydrological modeling of total dissolved phosphorus transport in an agricultural landscape, part II: dissolved phosphorus transport

International audienceReducing non-point source phosphorus (P) loss to drinking water reservoirs is a main concern for New York City watershed planners, and modeling of P transport can assist in the evaluation of agricultural effects on nutrient dynamics. A spatially distributed model of total dissolved phosphorus (TDP) loading was developed using raster maps covering a 164-ha dairy farm watershed. Transport of TDP was calculated separately for baseflow and for surface runoff from manure-covered and non-manure-covered areas. Soil test P, simulated rainfall application, and land use were used to predict concentrations of TDP in overland flow from non-manure covered areas. Concentrations in runoff for manure-covered areas were computed from predicted cumulative flow and elapsed time since manure application, using field-specific manure spreading data. Baseflow TDP was calibrated from observed concentrations using a temperature-dependent coefficient. An additional component estimated loading associated with manure deposition on impervious areas, such as barnyards and roadways. Daily baseflow and runoff volumes were predicted for each 10-m cell using the Soil Moisture Distribution and Routing Model (SMDR). For each cell, daily TDP loads were calculated as the product of predicted runoff and estimated TDP concentrations. Predicted loads agreed well with loads observed at the watershed outlet when hydrology was modeled accurately (R2 79% winter, 87% summer). Lack of fit in early spring was attributed to difficulty in predicting snowmelt. Overall, runoff from non-manured areas appeared to be the dominant TDP loading source factor

Distributed hydrological modelling of total dissolved phosphorus transport in an agricultural landscape, part I: distributed runoff generation

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The protective role of interleukin-10 in endotoxin shock.

Journal ArticleResearch Support, Non-U.S. Gov'tReviewinfo:eu-repo/semantics/publishe

Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia.

Because of its ability to efficiently inhibit in vitro cytokine production by activated macrophages, we hypothesized that interleukin (IL) 10 might be of particular interest in preventing endotoxin-induced toxicity. We therefore examined the effects of IL-10 administration before lipopolysaccharide (LPS) challenge in mice. A marked reduction in the amounts of LPS-induced tumor necrosis factor (TNF) release in the circulation was observed after IL-10 pretreatment at doses at low as 10 U. IL-10 also efficiently prevented the hypothermia generated by the injection of 100 micrograms LPS. Finally, pretreatment with a single injection of 1,000 U IL-10 completely prevented the mortality consecutive to the challenge with 500 micrograms LPS, a dose that was lethal in 50% of the control mice. We conclude that IL-10 inhibits in vivo TNF secretion and protects against the lethality of endotoxin in a murine model of septic shock.Journal ArticleResearch Support, Non-U.S. Gov'tSCOPUS: ar.jinfo:eu-repo/semantics/publishe

Interleukin-10 controls interferon-gamma and tumor necrosis factor production during experimental endotoxemia.

Interleukin-10 (IL-10) is a potent inhibitor of lipopolysaccharide (LPS)-induced tumor necrosis factor (TNF) production and has been shown to protect mice from endotoxin shock. As IFN-gamma is another important mediator of LPS toxicity, we studied the effects of IL-10 on LPS-induced IFN-gamma synthesis in vitro and in vivo. First, we found that the addition of recombinant human IL-10 (rhIL-10) (10 U/ml) to human whole blood markedly suppressed LPS-induced IFN-gamma release while neutralization of endogenously synthesized IL-10 resulted in increased IFN-gamma levels. The ability of rIL-10 to inhibit LPS-induced IFN-gamma synthesis was also observed in vivo in mice. Indeed, administration of 1000 U recombinant mouse IL-10 (rmIL-10) 30 min before and 3 h after challenge of BALB/c mice with 100 micrograms LPS resulted in a threefold decrease in peak IFN-gamma serum levels. We then examined the production and the role of IL-10 during murine endotoxemia. We found that LPS injection causes the rapid release of IL-10, peak IL-10 serum levels being observed 90 min after LPS challenge. Neutralization of endogenously produced IL-10 by administration of 2 mg JES5-2A5 anti-IL-10 monoclonal antibody (mAb) 2 h before LPS challenge resulted in a marked increase in both TNF and IFN-gamma serum levels while irrelevant isotype-matched mAb had no effect. The enhanced production of inflammatory cytokines in anti-IL-10 mAb-treated mice was associated with a 60% lethality after injection of 500 micrograms LPS, while all mice pretreated with control mAb survived. We conclude that the rapid release of IL-10 during endotoxemia is a natural antiinflammatory response controlling cytokine production and LPS toxicity.Journal ArticleResearch Support, Non-U.S. Gov'tFLWNAinfo:eu-repo/semantics/publishe