石头口门水库流域水污染物排放总量控制目标的确定方法研究

流域水污染物排放总量控制目标的确定是当前总量控制领域的研究热点。采用ReNuMa模型对石头口门水库流域建立了污染源—水质的定量响应关系,从径流量、总氮的模拟结果来看,模型的模拟精度满足要求。其次,建立了包括4部分内容(容量总量控制目标、规划年预测排污量、目标合理性因子、环境管理调控系数)的流域总氮总量控制目标确定模型。通过模型计算得到2020年石头口门水库流域总氮的总量控制目标为2.49万t。该总量控制目标确定模型统筹了目标总量控制与容量总量控制要求,兼具科学性与可行性。     

基于基尼系数的乌梁素海流域污染负荷分配

在水体污染物总量控制分配中,科学合理地分配污染物排放指标是实施水体环境管理的关键.将应用在经济领域衡量居民收入分配公平程度的基尼系数引入环境领域,提出环境基尼系数这一新概念用于解决流域内各分区污染物总量控制分配的问题.以乌梁素海流域为例,分别以流域内各分区人口、水资源量和国内生产总值(GDP)作为流域内基尼系数的分配指...     

陆海统筹的南流江流域污染物总量分配研究

综合考虑广西南流江流域陆域和廉州湾海域水质目标，遵循南流江流域、南流江河口、廉州湾近岸海域的污染路径，构建了基于陆海统筹的南流江流域污染物总量分配技术体系。首先，以廉州湾近岸海域环境功能区水质目标为约束条件，计算入海化学需氧量(COD)、氨氮、总氮(TN)和总磷(TP)的最大允许排放量，分别为24 494、3 425、10 052、776 t/a。然后以南流江河口最大允许排放量和南流江流域水功能区水质目标为约束条件，计算南流江流域陆域COD、氨氮、TN和TP的最大允许排放量，分别为126 365、5 403、8 939、1 127 t/a。为实现入海总量的控制目标要求，重点应在南流江流域削减污染物排放量，到2020年，南流江流域主要污染控制工程项目的削减能力已超过2020年污染物总量控制削减量，因此2030年实现南流江和廉州湾控制断面全面稳定达到相应功能区水质目标压力不大。     

天目湖富营养化现状研究

基于2005年天目湖(沙河水库)库体和取水口水质监测资料,分析其水库水质和富营养化状况.结果表明,全年水库透明度为3.10±0.14 m,总氮为0.455±0.036 mg/L,总磷为0.017±0.004 mg/L,N/P比的均值为28.8±9.5,浮游植物生长主要受营养盐磷的限制.采用总氮、总磷、透明度、高锰酸盐指数、溶解氧五项指标作为参数的富营养状态指数,评价结果表明,沙河水库水体营养水平较低,处于贫营养状态.     

三峡水库泄水期香溪河库湾营养盐动态及干流逆向影响

为了研究水库干流对支流库湾营养盐动态的影响,于2009年春季三峡水库汛前泄水期,通过监测分析了库湾水流特点及叶绿素a、总氮、总磷和溶解性硅酸盐的时空动态。研究发现:三峡水库汛前泄水期,库湾水体表现为分层异向流动,干流水体以异重流形式倒灌入库湾;特定的水流特性为泄水期库湾营养物质运移提供了水动力基础,水库干流对库湾营养盐的补给及水华暴发范围有明显逆向作用;受干流影响,氮和硅自河口至回水末端呈递减趋势,磷主要受上游来水影响,空间分布趋势与氮、硅相反;叶绿素a浓度峰值向上游移动,水华范围向上游收缩,河口处叶绿素a浓度的时间均值明显低于回水末端,表明三峡水库泄水期香溪河库湾下游水体水华受到干流逆向影响的抑制。     

青山水库底泥磷释放与库区水体磷浓度的关系

通过对青山水库底泥磷释放特性的实验结果分析,对照库区水体浓度监测的数据,确定了库区各测点底磷释放量与水体浓度之间的关系,进而为库区环境总量控制与各支流的分配计算提供了依据。同时也为防止水库的进一步富营养化,进而改善水质提供了新的思路。     

扬水曝气技术对周村水库藻类的控制

扬水曝气作为湖泊、水库水体修复技术之一,在国内多个水源水库水质改善工程中得到应用。为进一步研究扬水曝气技术对湖库藻类的控制效果及其机理,在对北方温带季节性分层水库-周村水库垂向水体的理化指标及藻类参数进行常年监测的基础上,于2015年8月—9月扬水曝气运行前后对垂向水体理化指标及浮游植物生物量、群落结构及丰度进行了连续监测和对比分析。结果表明,扬水曝气破坏了水体分层,藻类生物量锐减,多样性水平提高,藻类密度垂向差异消失,优势种群由威胁性较大的蓝藻、绿藻变为威胁性较小的硅藻,水体生态状况良好。扬水曝气系统对氮营养盐含量、热分层结构和光照条件的影响是促进了藻类群落结构改变的主要原因。     

水产养殖对水体富营养化的影响

通过对养殖水体和水库水体总氮（TN）、总磷（TP）含量的监测，分析了养殖污水排入前后的水库水体营养盐变化情况。从上游到下游的各点，营养指数有下降的趋势，由此得出结论，养殖污水的排入，是导致水库营养盐增加的主要原因，这为水库富营养化的治理提供了依据。     

海河流域水体沉积物中多氯联苯污染特征及风险评价

截至目前,尚没有研究从流域尺度系统分析海河流域水体沉积物中多氯联苯(PCBs)的污染特征及风险水平。以海河流域7大河系及典型湖库为研究对象,基于文献中PCBs的数据统计,从流域尺度探讨了不同水体沉积物中PCBs的组成和其空间分布特征,并利用潜在生态危害指数法和毒性当量法评价其生态风险。结果表明,海河流域水体沉积物总PCBs污染呈"北高南低"趋势。二氯联苯至十氯联苯在海河流域中都有不同程度的检出,主要以低氯原子数的二氯联苯至五氯联苯为主。海河流域沉积物中PCBs毒性主要取决于PCB-126和PCB-169。两种生态风险评价方法评价结果存在一定的不确定性,需将两种方法结合,进行综合判断。     

鸭河口水库水体总氮、总磷预测研究

根据鸭河口水库受纳点源及面源污染负荷情况，选择枯水期为预测时期，采用迪隆模型对鸭河口水库水体总氮、总磷进行预测研究，为鸭河口水库水质保持和富营养化防治提供基础数据。     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

A History of Dry Cleaners and Sources of Solvent Releases from Dry Cleaning Equipment

Approximately 25, 000-35, 000 dry cleaning facilities currently operate in the U.S. The release of perchloroethylene and other solvents from these establishments represents a major source of soil and groundwater contamination. The manner in which dry cleaning solvents escape from dry cleaning plants is, for all practical purposes, identical for chlorinated and petroleum hydrocarbon solvents and is related to one of the following events: the catastrophic failure of a component of the dry cleaning system, the improper installation, operation or maintenance of the dry cleaning equipment or a combination of all of these causes. Acceptable customs, codes and regulations can also dictate what is authorized for operation of a dry cleaning facility in a particular community, geographic area during a particular time frame. Environmental litigation dealing with the origin of a solvent release from dry cleaners tends to focus on the design and manufacture of dry cleaning industry machines such as washers, washer extractors, tumblers, solvent filters, water separators, stills and spotting boards. A thorough analysis of the daily operations of dry cleaners often reveals that poor maintenance, failure to follow the manufacturer's instructions and the actions of the operator are the most likely causes of soil and groundwater pollution. In order to forensically evaluate the most probable origins of a solvent release and to examine issues regarding liability, a thorough understanding of the history of dry cleaning and a detailed analysis of the operation and maintenance of the dry cleaning equipment are necessary. The discovery of solvent plumes in the vicinity of dry cleaning plants may suggest that the solvent source is the dry cleaning plant; however, the presence of these plumes does not necessarily indicate that the dry cleaning equipment was defectively designed or manufactured. A thorough review of the type of equipment used over the life of the dry cleaning plant and verifiable solvent mileage records frequently indicates that operators of the plant have disposed of solvent and contaminated solids into the municipal sewer or on ground surfaces.     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

Malathion-induced sublethal toxicity on the intestine of cricket frog (Fejervarya limnocharis)

The effect of malathion [diethyl(dimethoxythiophosphorylthio)succinate] at sublethal concentration (0.006 ppm) on intestinal parameters of cricket frog (Fejervarya limnocharis) was studied for 24 hrs to 240 hrs of exposure and remarkable histopathological alterations were observed. The study on intestinal parameters revealed acute pathological conditions in the intestinal wall. The toxic effect became evident as the cytoplasm of the cells disintegrated and the cells became empty and vacuolated. The cell membranes were also ruptured. Degenerative changes of the absorptive surface (villi) of the intestine in the different periods of exposure were pronounced. Severe atrophic nature (necrotic mucosa) of the intestine began from 48 hrs onwards to 96 hrs of exposure.     

Radionuclides in deer and elk from Los Alamos national laboratory and the doses to humans from the ingestion of muscle and bone

Abstract

This paper summarizes radionuclide concentrations (³H, ⁹⁰Sr, ¹³⁷Cs, ²³⁸Pu, ^239,240Pu, ²⁴¹Am, and ^totU) in muscle and bone tissue of mule deer (Odocoileus hemionus) and Rocky Mountain elk (Cervus elaphus) collected from Los Alamos National Laboratory (LANL), Los Alamos, New Mexico, lands from 1991 through 1998. Also, the committed effective dose equivalent (CEDE) and the risk of excess cancer fatalities (RECF) to people who ingest muscle and bone from deer and elk collected from LANL lands were estimated. Most radionuclide concentrations in muscle and bone from individual deer (n = 11) and elk (n = 22) collected from LANL lands were either at less than detectable quantities (where the analytical result was smaller than two counting uncertainties) and/or within upper (95%) level background (BG) concentrations. As a group, most radionuclides in muscle and bone of deer and elk from LANL lands were not significantly higher (p<0.10) than in similar tissues from deer (n = 3) and elk (n = 7) collected from BG locations. Also, elk that had been radio collared and tracked for two years and spent an average time of 50% on LANL lands were not significantly different in most radionuclides from road kill elk that have been collected as part of the environmental surveillance program. Overall, the upper (95%) level net CEDEs (the CEDE plus two sigma for each radioisotope minus background) at the most conservative ingestion rate (50 lbs of muscle and 13 lbs of bone) were as follows: deer muscle = 0.22 mrem y^‐1 (2.2 μSv y^‐1), deer bone = 3.8 mrem y^‐1 (38 μSv y^‐1), elk muscle = 0.12 mrem y^‐1 (1.2 μSv y^‐1), and elk bone = 1.7 mrem y^‐1 (17 μSv y^‐1). All CEDEs were far below the International Commission on Radiological Protection guideline of 100 mrem y^‐1 (1000 μSv y^‐1), and the highest muscle plus bone net CEDE corresponded to a RECF of 2E‐06, which is far below the Environmental Protection Agency upper level guideline of 1E‐04.     

Nitrogen leaching and acidification during 19 years of NH₄NO₃ additions to a coniferous-forested catchment at Gårdsjön, Sweden (NITREX)

The role of nitrogen (N) in acidification of soil and water has become relatively more important as the deposition of sulphur has decreased. Starting in 1991, we have conducted a whole-catchment experiment with N addition at Gårdsjön, Sweden, to investigate the risk of N saturation. We have added 41 kg N ha⁻¹ yr⁻¹ as NH₄NO₃ to the ambient 9 kg N ha⁻¹ yr⁻¹ in fortnightly doses by means of sprinkling system. The fraction of input N lost to runoff has increased from 0% to 10%. Increased concentrations of NO₃ in runoff partially offset the decreasing concentrations of SO₄ and slowed ecosystem recovery from acid deposition. From 1990-2002, about 5% of the total N input went to runoff, 44% to biomass, and the remaining 51% to soil. The soil N pool increased by 5%. N deposition enhanced carbon (C) sequestration at a mean C/N ratio of 42-59 g g⁻¹.     

Leaching of seven pesticides currently used in cotton crop in Mato Grosso State—Brazil

This study aimed to evaluate the leaching of pesticides and the applicability of the Attenuation Factor (AF) Model to predict their leaching. The leaching of carbofuran, carbendazim, diuron, metolachlor, α and β endosulfan and chlorpyrifos was studied in an Oxisol using a field experiment lysimeter located in Dom Aquino – Mato Grosso. The samples of percolated water were collected by rain event and analyzed. Chemical and physical soil attributes were determined before pesticide application to the plots. The results showed that carbofuran was the pesticide that presented a higher leaching rate in the studied soil, so was the one representing the highest contamination potential. From the total carbofuran applied in the soil surface, around 6 % leached below 50 cm. The other pesticides showed lower mobility in the studied soil. The calculated values to AF were 7.06E-12 (carbendazim), 5.08E-03 (carbofuran), 3.12E-17 (diuron), 6.66E-345 (α-endosulfan), 1.47E-162 (β-endosulfan), 1.50E-06 (metolachlor), 3.51E-155 (chlorpyrifos). AF Model was useful to classify the pesticides' potential for contamination; however, that model underestimated pesticide leaching.     

Endosulfan in China 2—emissions and residues

Background, aim, and scope  Endosulfan is one of the organochlorine pesticides (OCPs) and also a candidate to be included in a group of new persistent organic pollutants (UNEP 2007). The first national endosulfan usage inventories in China with 1/4° longitude by 1/6° latitude resolution has been reported in an accompanying paper. In the second part of the paper, we compiled the gridded historical emissions and soil residues of endosulfan in China from the usage inventories. Based on the residue/emission data, gridded concentrations of endosulfan in Chinese soil and air have been calculated. These inventories will provide valuable data for the further study of endosulfan. Methods  Emission and residue of endosulfan were calculated from endosulfan usage by using a simplified gridded pesticide emission and residue model—SGPERM, which is an integrated modeling system combining mathematical model, database management system, and geographic information system. By using the emission and residue inventories, annual air and soil concentrations of endosulfan in each cell were determined. Results and discussion  Historical gridded emission and residue inventories of α- and β-endosulfan in agricultural soil in China with 1/4° longitude by 1/6° latitude resolution have been created. Total emissions were around 10,800 t, with α-endosulfan at 7,400 t and β-endosulfan at 3,400 t from 1994 to 2004. The highest residues were 140 t for α-endosulfan and 390 t for β-endosulfan, and the lowest residues were 0.7 t for α-endosulfan and 170 t for β-endosulfan in 2004 in Chinese agricultural soil where endosulfan was applied. Based on the emission and residue inventories, concentrations of α- and β-endosulfan in Chinese air and agricultural surface soil were also calculated for each grid cell. We have estimated annual averaged air concentrations and the annual minimum and maximum soil concentrations across China. The real concentrations will be different from season to season. Although our model does not consider the transport of the insecticide in the atmosphere, which could be very important in some areas during some special time, the estimated concentrations of endosulfan in Chinese air and soil derived from the endosulfan emission and residue inventories are in general consistent with the published monitoring data. Conclusions  To our knowledge, this work is the first inventory of this kind for endosulfan published on a national scale. Concentrations of the chemical in Chinese air and agricultural surface soil were calculated for each grid cell. Results show that the estimated concentrations of endosulfan in Chinese air and soil agree reasonably well with the monitoring data in general. Recommendations and perspectives  The gridded endosulfan emission/residue inventories and also the air and soil concentration inventories created in this study will be updated upon availability of new information, including usage and monitoring data. The establishment of these inventories for the OCP is important for both scientific communities and policy makers.