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ABSTRACT: The purpose of this study was to evaluate the performance of Spatially Integrated Models for Phosphorus Loading and Erosion (SIMPLE) in predicting runoff volume, sediment loss, and phosphorus loading from two watersheds. The modeling system was applied to the 334 ha QOD subwatershed, part of the Owl Run watershed, located in Fauquier County, Virginia, and to the 2240 ha watershed, Battle Branch, located in Delaware County, Oklahoma. Simulation runs were conducted at cell and field scales, and simulation results were compared with observed data. Runoff volume and dissolved phosphorus loading were measured at the Battle Branch watershed. Runoff volume, sediment yield, and total phosphorus loading were measured at the QOD site. SIMPLE tended to underestimate runoff volumes during the dormant period, from November to March. The comparison between observed and predicted dissolved phosphorus showed better correlation than for observed and predicted total phosphorus loading. Cell level simulations provided similar estimates of runoff volume and phosphorus loading when compared to field level simulations for both watersheds. However, observed sediment yields better compared with the values predicted from the cell level simulation when compared to field level simulation. Finally, results of model evaluation indicated that SIMPLE's predictive ability is acceptable for screening applications but not for site-specific quantitative predictions.  相似文献   
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Objectives To validate the use of Real Time PCR, a widely used technique that can detect very low levels of Y chromosomal sequence, and to assess the use of a highly sensitive PCR technique, pyrophosphorolysis-activated polymerisation (PAP), for fetal sex determination using free fetal DNA (ffDNA). Methods The fetal sex was determined by Real Time PCR in 58 pregnancies using ffDNA isolated from maternal plasma. In parallel with the Real Time PCR experiments, the presence of Y chromosome sequence was also determined using PAP on 54 isolated ffDNA samples. Results Both techniques detected Y chromosome sequence at very low levels with 98% specificity and 100% sensitivity (Real Time n = 44, PAP n = 54). Furthermore, the PAP technique was shown to be more robust than the Real Time PCR as none of the samples tested failed to meet the acceptance criteria. Combining the two techniques for male fetal sex detection from maternal blood plasma increases the sensitivity and specificity to 100% in this series. Conclusions This study shows that both Real Time PCR and PAP can be used for Y chromosome detection on ffDNA. Furthermore, by using PAP in combination with Real Time PCR more reliable early prenatal sexing can be performed using ffDNA. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   
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