Groundwater Nitrate Concentration Reductions in a Riparian Buffer Enrolled in the NC Conservation Reserve Enhancement Program

Riparian buffers have been used for many years as a best management practice to decrease the effects of nonpoint pollution from watersheds. The NC Conservation Reserve Enhancement Program (NC CREP) has established buffers to treat groundwater nitrate‐nitrogen (NO₃^?‐N) from agricultural sources in multiple river basins. A maturing 46 m wide riparian buffer enrolled in NC CREP was studied to determine its effectiveness in reducing groundwater NO₃^?‐N concentrations from a cattle pasture fertilized with poultry litter. Three monitoring blocks that included groundwater quality wells, water table wells, and soil redox probes, were established in the buffer. NO₃^?‐N concentrations decreased significantly across the buffer in all of the monitoring blocks with mean reductions of 76‐92%. Many biological processes, including denitrification and plant uptake, may have been responsible for the observed NO₃^?‐N reductions but could not be differentiated in this study. However, mean reductions in Cl^? concentrations ranged from 48‐65% through the blocks, which indicated that dilution was an important factor in observed NO₃^?‐N reductions. These findings should be carefully considered for future buffer enrollments when assigning nitrogen removal credits.     

Critical Loads Exceedances in Germany and their Dependence on the Scale of Input Data

Critical load exceedances have been used as an effects-related parameter for guiding international air emission control negotiations. High-resolution critical load data are combined with low-resolution deposition data.This article shows that doing so systematicallyunderestimates `true' critical load exceedances as obtainedfrom combining critical load and deposition data of identicalhigh spatial resolution. 95th percentile critical loadexceedances in EMEP grids based on high resolution depositiondata are 60 and 150% higher (mean values for nutrientnitrogen and acidity, respectively) than critical loadexceedances based on the low resolution EMEP depositionmodel. The latter are used in international negotiations. Differences in individual EMEP grid squares vary betweeninsignificantly different from zero and 340%, depending onregional deposition and critical load characteristics andcritical load types (nutrient nitrogen versus acidity).Exceedances based on high-resolution deposition values arealso compared to EMEP grid averages of these values forforests only. This comparison excludes the effect ofsystematically higher depositions to forests. Still, thescale difference of (averaged, low-resolution) deposition and(high-resolution) critical loads data yields underestimatesof the 95th percentiles by on average ca. 20%.These systematic errors due to the scale dependence should beborne in mind when interpreting effects of internationalemission control measures.     

对影响高锰酸盐指数测定的重要因子--K值的探讨

高锰酸盐指数是水质监测中常规项目 ,在实际测定中 ,K值的大小直接影响测定过程。本文对K值进行讨论 ,并提出解决办法     

多孔喷头射流特性的实验研究

在没有密度分层的容泄水体条件下,对某污水排海工程多孔喷头的射流特性进行了实验研究。文中介绍了不同排污流量和环境流速条件下,多孔喷头附近的流速场和污水场特性;并对出流平均稀释度作了分析。最后,还对该喷头周围的冲淤形态进行了探讨.文中所得的结果对实际排污系统的设计和进一步研究有一定的参考价值。      

应用概率稀释模型计算允许纳污量

进一步剖析了引进的概率稀释模型,考虑了上游来水浓度CS,在理论上完整地体现了物质平衡基本原理,提高了模型的科学性和正确性,使设计条件更加接近于我国的实际情况(CS≠0),使应用性和可操作性大大提高。      

Soilaluminum, Iron, and Phosphorus Dynamics in Response to Long-Term Experimental Nitrogen and Sulfur Additions at the Bear Brook Watershed in Maine, USA

Atmospheric deposition of nitrogen (N) and sulfur (S) containing compounds affects soil chemistry in forested ecosystems through (1) acidification and the depletion of base cations, (2) metal mobilization, particularly aluminum (Al), and iron (Fe), (3) phosphorus (P) mobilization, and (4) N accumulation. The Bear Brook Watershed in Maine (BBWM) is a long-term paired whole-watershed experimental acidification study demonstrating evidence of each of these acidification characteristics in a northeastern U.S. forested ecosystem. In 2003, BBWM soils were studied using the Hedley fractionation procedure to better understand mechanisms of response in soil Al, Fe, and P chemistry. Soil P fractionation showed that recalcitrant P was the dominant fraction in these watersheds (49%), followed by Al and Fe associated P (24%), indicating that a majority of the soil P was biologically unavailable. Acidification induced mobilization of Al and Fe in these soils holds the potential for significant P mobilization. Forest type appears to exert important influences on metal and P dynamics. Soils supporting softwoods showed evidence of lower Al and Fe in the treated watershed, accompanied by lower soil P. Hardwood soils had higher P concentrations in surface soils as a result of increased biocycling in response to N additions in treatments. Accelerated P uptake and return in litterfall overshadowed acidification induced P mobilization and depletion mechanisms in hardwoods.     

Inter-Laboratory Comparison of No2 and SO2 Generated by Dynamic Dilution System Under Laboratory Conditions: A Technical Discussion

A workshop on analytical quality control (AQC) of ambient air quality measurement methods for nitrogen dioxide (NO₂) and sulphur dioxide (SO₂) was conducted by Central Pollution Control Board (CPCB) for officials involved in National Ambient Air Quality Monitoring (NAAQM) in India. Concentrations of NO₂ and SO₂ were generated by dynamic dilution system under laboratory conditions at low and high levels and measured using static dilution system and wet chemical methods laid down by CPCB under section 16(2)(h) of the air act 1981. CPCB provided the measured values as reference values for comparing the means obtained by the officials participated from thirteen organizations. A tolerance limit of ±15% of the reference values was specified to accept the results. Generated concentrations, which were unknown to the participants, were measured using gaseous sampling assembly (Envirotech APM 411, New Delhi, India), and wet chemical methods laid down by CPCB i.e. the same methodology which is used by the organizations to generate the data of NO₂ and SO₂ in ambient air. Simultaneously, concentrations were checked by CPCB using automatic analyzers as a check on reference concentration. It is observed that results of automatic analyzers for NO₂ and SO₂ were within a tolerance of ±5% with %RSD below 3. On the other hand, results of most of the participants showed variability in the measurements with %RSD ranging between ±0.8 and ±88.6 and exceedences of means from the tolerance limit with bias ranging between 1.4 and −59%. To check the cause of high variability in the measurements obtained under identical conditions, duplicate sampling was performed by one of the participants for SO₂ at low concentration level. In this study, results of wet chemical methods, automatic analyzers and results of duplicate sampling are analysed statistically to assess the cause of high variability in the measurements. Analysis of t-test and analysis of variance (ANOVA) showed highly significant results for NO₂ and SO₂ at high concentration levels (α 0.05) and for SO₂ at both the levels (α 0.01) respectively indicating some bias is existing either in the sampling or in analytical technique. Duplicate sampling performed to check precision in parallel measurements showed high %RSD indicating the presence of systematic error in sampling technique as the same calibration factor (CF) was used to measure the concentration of duplicate samples. Statistical analysis of flow rates of duplicate sampling showed that the sampling assembly could not maintain the constant flow rate within the ±10% with that measured at the start of the sampling. This resulted in high %RSD and deviation from the reference values for the results of most of the participants, even after accepting ±15% tolerance limit. There is a need to improve and evaluate this gaseous sample collection device under laboratory conditions to generate reliable database of NO₂ and SO₂ in ambient air.     

ABR反应器处理低浓度污水启动试验研究

为了探讨了四室ABR反应器启动规律,以低浓度污水为研究对象,通过控制酸化菌INT比脱氢酶活性、酸化率、OLR和H RT来实现反应器内部微生物相分离。结果表明:在水力停留时间3h,有机负荷2.4kgCOD/(m 3.d)条件下,酸化菌INT比脱氢酶活性与酸化率有关,且随流向逐渐降低,同一格室内中部比INT脱氢酶活性高于底部;一室、二室的酸化率占总酸化率的70%,确定一、二室为产酸反应器,三、四室为产甲烷反应器,实现了微生物相分离;反应器的启动时间为18d,稳定运行时,COD去除率可以达到35%￣40%。     

采用商业混合菌种测定BOD5的可行性

通过实验,对比研究了采用商业混合菌种（Polyseed）改进传统方法测定BOD5的可行性。研究结果表明,相比于采用地表水作为接种水的传统方法,采用进口商业混合菌种配制接种稀释水BOD5（空白值）更稳定,可以改进传统BOD5测定方法,使得日常监测工作更为便捷。