Application of statistical modeling to optimize a coastal water quality monitoring program

The long-term water quality monitoring program implemented by the Massachusetts Water Resources Authority in 1992 is extensive and has provide substantial understanding of the seasonality of the waters in both Boston Harbor and Massachusetts Bay and the response to improvements in effluent quality and offshore transfer of the effluent in September 2000. The monitoring program was designed with limited knowledge of spatial and temporal variability and long-term trends within the system. This led to an extensive spatial and temporal sampling program. The data through 2003 showed high correlation within physical parameters measured (e.g., salinity, dissolved oxygen) and in biological measures such as chlorophyll fluorescence. To address the potential sampling redundancies in the measurement program, an assessment of the impact of reduced levels of monitoring on the ability to make water quality decisions was completed. The optimization was conducted by applying statistical models that took into account whether there was evidence of a seasonal pattern in the data. The optimization used model survey average readings to identify temporal fixed effects, model survey-average-corrected individual station readings to identify spatial fixed effects, corrected the individual station readings for temporal and spatial fixed effects and derived a correlation model for the corrected data, and applied the correlation model to characterize the correlation of annual average readings from reduced monitoring programs with true parameter levels. Reductions in the number of sampling stations were found less detrimental to the quality of the data for annual decision-making than reductions in the number of surveys per year, although there is less of a difference in this regard for dissolved oxygen than there is for chlorophyll. The analysis led to recommendations for a substantially lower monitoring effort with minimal loss of information. The recommendation supported an annual budget savings of approximately $183,000. Most of the savings was from fewer surveys as approximately $21,000 came from the reduction in the number of stations monitored from 21 to 7 and associated laboratory analytical costs.     

连续采样与五日法采样效果及费用的对比分析

通过对连续采样与五日法采样五种方法监测结果及所需费用的比较，得出连续采样方法监测结果更具有代表性，合理性，一次性投资大，但运行费用并不高的结论。     

环境监测能力建设与仪器支撑

在总结我国环境监测技术和仪器发展的基础上,从"十二五"环境监测工作发展的需要,阐明了我国环境监测技术和监测仪器存在的问题以及未来的发展趋势。     

应用流式细胞仪监测太湖藻类初探

流式细胞仪在海水微型浮游生物监测领域应用较为广泛,但在淡水藻类定量研究以及生物监测中应用仍较少。探讨了应用便携式浮游植物流式细胞仪CytoSense监测太湖藻类的可行性和时效性。结果表明,为了提高检测结果的准确性,流式细胞仪的应用过程中最好是现场采样、现场分析。流式细胞仪对藻细胞密度的检测下限为100万个/L,大于100万个/L时检测结果与人工镜检结果相吻合;在悬浮物含量小于108 mg/L的水体中,流式细胞仪检测结果具备较高的准确性。另外,流式细胞仪操作简单、分析速度快、便携性好、无污染,在太湖藻类监测中具有一定应用前景。     

Spatiotemporal trends of PM2.5 and its major chemical components at urban sites in Canada

To evaluate the effectiveness of emission control regulations designed for reducing air pollution, chemically resolved PM_2.5 data have been collected across Canada through the National Air Pollution Surveillance network in the past decade. 24-hr time integrated PM_2.5 collected at seven urban and two rural sites during 2010-2016 were analyzed to characterize geographical and seasonal patterns and associated potential causes. Site-specific seven-year mean gravimetric PM_2.5 mass concentrations ranged from 5.7 to 9.6 µg/m³. Seven-year mean concentrations of SO₄^2?, NO₃^?, NH₄⁺, organic carbon (OC), and elemental carbon (EC) were in the range of 0.68 to 1.6, 0.21 to 1.5, 0.27 to 0.71, 1.1 to 1.9, and 0.37 to 0.71 µg /m³, accounting for 10.8%-18.1%, 3.7%-16.7%, 4.7%-7.4%, 18.4%-21.0%, and 6.4%-10.6%, respectively, of gravimetric PM_2.5 mass. PM_2.5 and its five major chemical components showed higher concentrations in southeastern Canada and lower values in Atlantic Canada, with the seven-year mean ratios between the two regions being on the order of 1.7 for PM_2.5 and 1.8-7.1 for its chemical components. When comparing the concentrations between urban and rural sites within the same region, those of SO₄^2? and NH₄⁺ were comparable, while those of NO₃^?, OC, and EC were around 20%, 40%-50%, and 70%-80%, respectively, higher at urban than rural sites, indicating the regional scale impacts of SO₄^2? and NH₄⁺ and effects of local sources on OC and EC. Monthly variations generally showed summertime peaks for SO₄^2? and wintertime peaks for NO₃^?, but those of NH₄⁺, OC, and EC exhibited different seasonality at different locations.     

地表水环境监测进展与问题分析

地表水环境的质量监测对我国水环境保护工作具有非常重要的作用,同时对我国的经济发展有着深远的影响。随着我国经济的快速发展,我国水环境监测工作有了较大的发展,但是在仪器更新、分析能力等方面还存在一系列的问题,本文对地表水环境监测的进展进行了阐述,并分析了水环境监测中存在的问题。     

A GIS Model of Subsurface Water Potential for Aquatic Resource Inventory,Assessment, and Environmental Management

Biological, chemical, and physical attributes of aquatic ecosystems are often strongly influenced by groundwater sources. Nonetheless, widespread access to predictions of subsurface contributions to rivers, lakes, and wetlands at a scale useful to environmental managers is generally lacking. In this paper, we describe a neighborhood analysis approach for estimating topographic constraints on spatial patterns of recharge and discharge and discuss how this index has proven useful in research, management, and conservation contexts. The Michigan Rivers Inventory subsurface flux model (MRI-DARCY) used digital elevation and hydraulic conductivity inferred from mapped surficial geology to estimate spatial patterns of hydraulic potential. Model predictions were calculated in units of specific discharge (meters per day) for a 30-m²-cell raster map and interpreted as an index of potential subsurface water flux (shallow groundwater and event through-flow). The model was evaluated by comparison with measurements of groundwater-related attributes at watershed, stream segment, and local spatial scales throughout Lower Michigan (USA). Map-based predictions using MRI-DARCY accounted for 85% of the observed variation in base flow from 128 USGS gauges, 69% of the observed variation in discharge accrual from 48 river segments, and 29% of the residual variation in local groundwater flux from 33 locations as measured by hyporheic temperature profiles after factoring out the effects of climate. Although it does not incorporate any information about the actual water table surface, by quantifying spatial variation of key constraints on groundwater-related attributes, the model provides strata for more intensive study, as well as a useful spatial tool for regional and local conservation planning, fisheries management, wetland characterization, and stream assessment.     

一个填埋场的气体排放控制系统的建立及其从中得到的几点启示

介绍位于纽约州北汉姆斯特城的ＰｏｒｔＷａｓｈｉｎｇｔｏｎ城市固体废弃物填埋场填埋气体的排放、监测和处理系统及其有关测试数据和从中得到的启示．     

Runoff of pesticides from rice fields in the Ile de Camargue (Rhône river delta, France): field study and modeling

A field study on the runoff of pesticides was conducted during the cultivation period in 2004 on a hydraulically isolated rice farm of 120 ha surface with one central water outlet. Four pesticides were studied: Alphamethrin, MCPA, Oxadiazon, and Pretilachlor. Alphamethrin concentrations in runoff never exceeded 0.001 microg L(-1). The three other pesticides were found in concentrations between 5.2 and 28.2 microg L(-1) in the runoff water shortly after the application and decreased thereafter. The data for MCPA compared reasonably well with predictions by an analytical runoff model, accounting for volatilization, degradation, leaching to groundwater, and sorption to soil. The runoff model estimated that runoff accounted for as much as 18-42% of mass loss for MCPA. Less runoff is observed and predicted for Oxadiazon and Pretilachlor. It was concluded that runoff from rice paddies carries important loads of dissolved pesticides to the wetlands in the Ile de Camargue, and that the model can be used to predict this runoff.     

Trimethylbenzoic acids as metabolite signatures in the biogeochemical evolution of an aquifer contaminated with jet fuel hydrocarbons

Evolution of trimethylbenzoic acids in the KC-135 aquifer at the former Wurtsmith Air Force Base (WAFB), Oscoda, MI was examined to determine the functionality of trimethylbenzoic acids as key metabolite signatures in the biogeochemical evolution of an aquifer contaminated with JP-4 fuel hydrocarbons. Changes in the composition of trimethylbenzoic acids and the distribution and concentration profiles exhibited by 2,4,6- and 2,3,5-trimethylbenzoic acids temporally and between multilevel wells reflect processes indicative of an actively evolving contaminant plume. The concentration levels of trimethylbenzoic acids were 3-10 orders higher than their tetramethylbenzene precursors, a condition attributed to slow metabolite turnover under sulfidogenic conditions. The observed degradation of tetramethylbenzenes into trimethylbenzoic acids obviates the use of these alkylbenzenes as non-labile tracers for other degradable aromatic hydrocarbons, but provides rare field evidence on the range of high molecular weight alkylbenzenes and isomeric assemblages amenable to anaerobic degradation in situ. The coupling of actual tetramethylbenzene loss with trimethylbenzoic acid production and the general decline in the concentrations of these compounds demonstrate the role of microbially mediated processes in the natural attenuation of hydrocarbons and may be a key indicator in the overall rate of hydrocarbon degradation and the biogeochemical evolution of the KC-135 aquifer.