流动注射-氢化物发生-原子吸收法测定土壤中微量砷

用混酸消解土壤试样，用体积分数为20％的盐酸作酸介质，质量分数为1．5％的硼氢化钾作还原剂，体积分数为1％的盐酸作载液，采用流动注射-氢化物发生三-原子吸收法定量测定土壤中的微劈砷。通过实验确定，在原子化温度为920℃、土壤中共存元素含量低于5mg／kg时对测定无干扰。该方法的榆出限为0．5μg/L，线性范嘲为5～100μg/L．相对标准偏差为0．89％，平均回收率达98．99％：     

流动注射分光光度法测定水中铝的含量

以桑色素作显色剂，采用流动注射分光光度法测定水中铝的含量。在桑色素质量浓度为0．8g／L、聚氧乙烯辛基苯基醚体积分数为1．0％、进样环体积为400μL、检测波长420nm的条件下，采用流动注射分光光度法对水中铝的含量进行测定，本方法的线性范围为2～300μg／L，检出限（信噪比为3）为0．124μg／L，相对标准偏差为2．9％，加标回收率为96．4％～101．8％。     

气相色谱法测定水和土壤中苯醚甲环唑的残留量

研究并建立了气相色谱法测定水和土壤中苯醚甲环唑残留量的分析方法。实验结果表明：水中添加苯醚甲环唑的含量为0．005～0．500mg／kg时，平均回收率为97．9％～100．5％，相对标准偏差小于6．7％；土壤中添加苯醚甲环唑的含量为0．005～0．500mg／kg时，平均回收率为95．7％～109．5％，相对标准偏差小于7．5％。将该法用于水和土壤残留实验，土壤试样在拖药后10～88d进行采样分析，其残留消解动态回归方程为y=0．8803e^-0.0122x，相关系数为-0．915，消解半衰期为56．8d；水试样在施药后0～21d进行采样分析，其残留消解动态回归方程为y=0．2624e^-0.2539x，相关系数为-0．899，消解半衰期为2．7d。     

固相萃取-气相色谱法检测水中的邻苯二甲酸酯

利用固相萃取技术富集了水中4种邻苯二甲酸酯类（PAEs）化合物：邻苯二甲酸二甲酯（DMP）、邻苯二甲酸二乙酯（DEP）、邻苯二甲酸二丁酯（DBP）、邻苯二甲酸二（2-乙基己基）酯（DEHP）。借助均匀设计法及计算机回归建模优化技术对4种PAEs的固相萃取条件进行了设计与优化，得到的最佳固相萃取条件：洗脱剂配比（正己烷与丙酮的体积比）30：1，洗脱体积2mL，洗脱速率4mL／min，上样速率8mL／min。富集后的试样用带电子捕获器的毛细管气相色谱仪检测，方法的线性范围为1～1000μg／L（DMP，DEP），0．2—100μg／L（DBP，DEHP），线性回归方程的相关系数为0．9970～1．0000，检出限为0．02-0．4μg／L，4种PAEs的回收率为69％～117％，相对标准偏差为2．5％～9．5％。[关键词]     

火焰原子吸收光度法测定水中铝的方法改进

研究了在盐酸介质中，壬基酚聚氧乙烯-7醚（NP-7）活化下，火焰原子吸收光度法测定环境水体中铝的方法改进。在25mL容量瓶中，加入5．0mL体积分数为50％的盐酸、2．0mL质量浓度为0．01g／mL NP-7和4．0mL质量浓度为75．0μg/mL的铝标准溶液，在原子吸收分光光度计的最佳测定条件下测定吸光度。根据吸光度与铝质量浓度绘制了工作曲线，线性范围3．0～24．0μg/mL，检出限1．32μg/mL。该法用于环境水体中铝含量的测定，加标回收率为94．4％～101．4％，最大相对标准偏差5．8％，方法对比最大相对误差4．1％。     

流动注射在线富集分光光度法测定水样中痕量Cr(Ⅵ)

采用流动注射在线富集分光光度法测定水样中痕量Cr（Ⅵ），考察了流路条件、显色条件和共存离子的影响。在H：SO。浓度为1．2mol/L、2-（5-溴-2-吡啶偶氮）-5-二乙氨基酚溶液质量浓度为1．75g／L的条件下，试样富集4min，测定Cr（Ⅵ）的线性范围为0．01～0．60mg／L，检出限为3μg/L。连续10次测定质量浓度为0．20mg／L的Cr（Ⅵ）标准溶液相对标准偏差为0．4％。方法可应用于河水和工业废水中痕量Cr（Ⅵ）的测定，加标回收率为93．3％～106．4％。     

自动进样气相色谱法测定气体中的非甲烷烃

用泰德拉气体采样袋采样，自动进样气相色谱法测定气体中的非甲烷烃含量。甲烷、总烃的线性范围分别为0～2439，0—2066mg／m^3。进样量为1mL时，检出限为0．02mg／m^3（信噪比为3）。对3种不同浓度甲烷与丙烷混合标准气进行测定，重复性相对标准偏差为0．4％-1．0％。对4种不同性质的试样进行加标回收实验，加标回收率为96．7％-102．0％。5名实验人员分别用自动进样法及手动进样法分析4种不同性质的试样，自动进样法的重现性相对标准偏差为1．2％～1．8％，优于手动进样法的6．5％～8．3％。该法可一次连续测定21个试样，精密度高、重现性好、分析效率高。     

利用磷化渣配制复合磷化液

采用固体废物磷化渣配制成复合磷化液，并用所配制的复合磷化液对A3钢试件进行磷化处理，形成磷化膜。通过正交实验确定了配制复合磷化液的较佳配方为：磷化液基础液加入量0．2L／L、氧化锌加入量5g／L、碳酸钠加入量6g／L、硝酸加入量12．5mL／L、浓磷酸加入量2．5mL／L、硫酸铜加入量0．3g／L。复合磷化液为浅绿色透明溶液，pH为4．0，总酸度为40，游离酸度为10，磷化温度为65℃，磷化时间为300～600s。所形成的磷化膜厚度为16．0μm，单位质量为26．875g／m^2，粗糙度为1．425μm，维氏硬度为124．27kgf／mm^2。磷化膜硫酸铜点滴时间为35s，耐盐水时间为8h，耐盐雾时间为4h，其物理性质和耐蚀性能均较佳。     

石油污染土壤的生物修复技术研究

通过实验室选择性富集培养，从大庆石油污染土壤中获得了能以大庆原油为碳源快速生长的石油降解菌。采用该降解菌对原油污染土壤进行了原位生物联合修复实验。接入降解菌的处理单元分别种植大豆、碱草或加入蓬松剂，与空白试样作对比。各处理单元石油污染土壤中石油烃含量初始值为2228．25mg／kg（以1kg干土计）。经过135d的生物联合修复，石油烃降解率达63．65％-83．26％。     

用高效液相色谱法分析精对苯二甲酸残渣

用高效液相色谱法分析精对苯二甲酸残渣，考察了适宜的操作条件。实验结果表明，在采用阴离子交换柱作分析柱，浓度为0．2mol／L的磷酸二氢铵缓冲液为流动相、体积分数为10％的甲醇作有机改性剂、用磷酸调试样pH为6—7、检测波长为240nm的最佳条件下，分离效果最好，对羧基苯甲醛、苯甲酸、对甲基苯甲酸、邻苯二甲酸、对苯二甲酸、间苯二甲酸、1，2，4-苯三酸、1，3，5-苯三酸的加标回收率分别为98．39％，98．81％，98．66％，97．73％，98．93％，98．90％，98．25％，98．40％。相对标准偏差分别为0．87％，0．49％，0．76％，0．88％，0．71％，0．46％，0．63％，0．47％，方法的检出限分别为0．1，0．2，0．1，0．4，0．1，0．4，0．6，2．0mg／L，线性范围分别为0．88-17．50，1．48～29．60，1．47～29．30，1．34～26．80，1．79～35．80，2．70～53．90，2．98～59．50，3．00～59．90mg／L。     

Programs assessing implementation and effectiveness of state forest practice rules and BMPs in the West

The major forest nonpoint source control programs in the West are largely regulatory, either under forest practices acts (California, Idaho, New Mexico, Nevada, Oregon, and Washington) or a streamside management act (Montana). These programs and the specific rules they enforce continue to undergo intensive scrutiny. Still, the questions are the same for these regulatory programs as for states that base nonpoint source control on voluntary BMPs (Arizona, Colorado, Utah, Wyoming). Are the rules or BMPs being applied, and are they effective in reducing nonpoint source pollution to levels that protect beneficial uses of water? The level of debate about forestry in the West has resulted in detailed monitoring and research to answer these questions. In the past, state agencies have assumed levels of BMP compliance based on the percent of operations without enforcement actions. These estimates are being replaced by statistically valid and reproducible monitoring of forest practices rules and BMP compliance levels. BMP effectiveness is being assessed using both qualitative and quantitative methods. This can involve field assessments, process-based research, and control watershed studies. Some trend monitoring is also beginning. With the regional implementation rate for forestry BMPs at about 94% and rising, it is likely that effectiveness testing will continue to be a priority and consume the majority of assessment resources for this region.     

Hysteresis in Reversal of Central European Mountain Lakes from Atmospheric Acidification

Extremely high emissions of S and N compounds in Central Europe (both 280 mmol m^-2 yr^-1) declined by 70and 35%, respectively, during the last decade. Decreaseddeposition rates of SO₄ ^-2, NO₃ ^-, and NH₄ ⁺ in the region paralleled emission declines. The reduction in atmospheric inputs of S and N to mountain ecosystemshas resulted in a pronounced reversal of acidification in the Tatra Mountains and Bohemian Forest lakes. Between the 1987–1990and 1997–1999 periods, concentrations of SO₄ ^-2 and NO₃ ^- decreased (average ± standard deviation) by 22±7 and 12±7 mol L^-1, respectively, in theTatra Mountains, and by 19±7 and 15±10 mol L^-1, respectively, in the Bohemian Forest. Their decrease was compensated in part (1) by a decrease in Ca²⁺ + Mg²⁺ (17±7 mol L^-1) and H⁺ (4±6 mol L^-1), and an increase in HCO₃ ^-(10±10 mol L^-1) in the Tatra Mountains lakes, and (2) by a decrease in Al (7±4 mol L^-1), Ca²⁺ + Mg²⁺ (9±6 mol L^-1), and H⁺ (6±5 mol L^-1), in Bohemian Forest lakes. Despite the rapid decline in lake water concentrations of SO₄ ^-2 and NO₃ ^- in response to reduced S and N emissions, their present concentrations in some lakes are higher than predictionsbased on observed concentrations at comparable emission rates during development of acidification. This hysteresis in chemical reversal from acidification has delayed biological recovery of the lakes. The only unequivocal sign of biological recovery hasbeen observed in erné Lake (Bohemian Forest) where a cladoceran species Ceriodaphnia quadrangular has recentlyreached its pre-acidification abundance.     

Reconstruction of Long-Term Changes in Lake water Chemistry,Zooplankton and Benthos of a Small,Acidified High-Mountain Lake: Magic Modelling and Palaeolimnogical Analysis

Starolesnianske pleso is a small and shallow acid lake in the High Tatra Mountains, situated at 2000 m above sea level, on granitic bedrock, with sparse and thin soil cover. When detailed measurements began in the 1980s Starolesnianske pleso had pH below 5 and only one species of cladoceran zooplankton, the ubiquitous Chydorus sphaericusPalaeolimnological investigations show changes in cladoceran zooplankton and chironomid zoobenthic assemblages since about 1920 and a major change in 1970–1980. The dynamic acidification model MAGIC was used to reconstruct changes in water chemistry over the past 150 years. The results from MAGIC agree well with the sediment record; pH levels gradually decreased from 6.5 in the mid-1800s to about 5.6 in 1920 (first response in biota) to below 5.0 by 1970, and concentrations of inorganic aluminium rose dramatically beginning about 1960. In the 1990s the lake water chemistry showed clear signs of reversal in acidification brought about by a major decline in S deposition.     

Heavy Metals Removal by Biosorption and Flotation

The removal of a mixture of heavy (toxic) metal cations (copper, nickeland zinc) from liquid effluents was investigated in this study at pilotscale, using counter-current contact mode. The innovative processinvolved the abstraction of metal ions onto fungal biosorbents, followedby the application of flotation for the subsequent solid/liquid separationof biomass particles. The ability of microorganisms to remove metal ionsfrom aqueous solutions is a well-known phenomenon. Nevertheless,engineering considerations are very important in decisions, concerningthe commercial future of biosorption and practical solutions are neededfor certain problems, such as the efficient post-separation ofmetal-loaded biomass. The two processes (flotation and biosorption) caneffectively operate in combination, in what it was termed biosorptiveflotation process. The sorbents may be recycled, after appropriate elutionof metals, as well as the treated (clean) water.     

Selection of Autochthonous Plant Species from SE Spain for Soil Lead Phytoremediation Purposes

Mining activity in SE of Spain, in the west Mediterranean coast, originated more than two millenniums ago. It has generated huge areas affected by heavy metals contamination, especially of lead, which is possibly one of the most important. Investigations related to the selection of autochthonous plant taxa from a typical Spanish Mediterranean area, useful for phytoextraction and phytostabilization purposes in these polluted areas are shown. Under these edaphoclimatic conditions 12 interesting species were considered, from them six taxa were chosen for further studies. Some plant species have been proposed either for phytoextraction or phytostabilization purposes. Recommendations for further research have been discussed.     

Concentrations and Pools of Heavy Metals in Urban Soils in Stockholm,Sweden

The concentrations of heavy metals (Cd, Cr, Cu, Hg, Ni, Pb andZn) and arsenic (As) were surveyed and the metal pools estimatedin soils in Stockholm Municipality. The sampling sites were distributed all over the entire municipality with a higher sampling density in the city centre. Soils were sampled to a maximum depth of 25 to 60 cm. Soil texture, total-C content, electrical conductivity and pH were analysed. Heavy metal concentrations were determined after wet digestion with boiling7 M HNO₃.The results showed a wide range in heavy metal concentrations, as well as in other soil properties. The city centre soils constituted a rather homogeneous group whereas outside this areano geographical zones could be distinguished. These soils were grouped based on present land use, i.e. undisturbed soils, public parks, wasteland (mainly former industrial areas), and roadside soils. The city centre and wasteland soils generally hadenhanced heavy metal concentrations to at least 30 cm depth compared to park soils outside the city centre and rural (arable)soils in the region, which were used to estimate background levels. For example, the mean Hg concentration was 0.9 (max 3.3)mg kg^-1 soil at 0–5 cm and 1.0 (max 2.9) at 30 cm depth in the city centre soils, while the background level was 0,04 mg kg^-1. Corresponding values for Pb were 104 (max 444) and135 (max 339) mg kg^-1, at 0–5 and 30 cm, respectively, while the background level was 17 mg kg^-1.The average soil pools (0–30 cm depth) of Cu, Pb and Zn were 21,38 and 58 g m^-2 respectively, which for Pb was 3–4 timeshigher and for Cu and Zn 1.5–2 times higher than the backgroundlevel. The total amount of accumulated metals (down to 30 cm)in the city centre soils (4.5^*10 ⁶ m² public gardens and green areas) was estimated at 80, 1.1, 120 and 40 t for Cu, Hg, Pb and Zn, respectively. The study showed (1) thatfrom a metal contamination point of view, more homogeneous soilgroups were obtained based on present land use than on geographicdistance to the city centre, (2) the importance of establishing a background level in order to quantify the degree of contamination, and (3) soil samples has to be taken below the surface layer (and deeper than 30 cm) in order to quantify theaccumulated metal pools in urban soils.     

我国电子废物回收处理产业政策及机遇与挑战分析

针对近年我国频繁出台的电子废物回收处理产业政策,系统论述了其发展脉络,并从循环经济角度出发,分析了我国电子废物产业发展的主体思路,同时还对我国电子废物回收处理产业发展机遇与存在的问题进行剖析,对如何稳定企业的电子废物来源、提升产业技术水平及降低企业运营成本进行建议性分析。     

Nitrous oxide emission from some English and Welsh rivers and estuaries

Nutrient and N₂O concentrations in the water columns were measured seasonally over a full salinity range in the nutrified rivers Colne, Stour, Orwell, Deben, Trent, Ouse and Humber and their estuaries on the east coast of England between August 2001 and May 2002, and in the oligotrophic rivers Conwy, Dovey and Mawddach in North and West Wales between August 2002 and May 2003. Nutrient and N₂O concentrations in the nutrified English rivers and estuaries were much higher than those in the Welsh rivers. N₂O concentrations and % saturation in the estuaries were significantly correlated with nitrate, nitrite and ammonium concentrations in the water. The strongest correlation was with nitrite (r² = 0.56, p < 0.01), suggesting that nitrite was the most significant factor among the different nutrients in regulating N₂O concentration in the estuaries. N₂O concentrations in the English rivers and estuaries were supersaturated throughout the year with annual averages from 186.9 to 992.9%, indicating that these rivers and estuaries were sources of atmospheric N₂O, whereas in the Welsh rivers N₂O concentrations were much lower with annual averages from 113.6 to 137.4% saturation. Although the estuarine area in the Colne was almost the same as that in the Conwy, the annual N₂O emission from the Colne was much higher (937498 mol N yr^–1) than in the Conwy (23020 mol N yr^–1). On the east coast, riverine emissions of N₂O were only 0.5–12.5% of the total emission from rivers and estuaries. Thus rivers were negligible, but estuaries were significant contributors to the UK N₂O inventory.     

Trends in Fish Community Structure,Biomass, and Production in Three Algoma,Ontario, Lakes

Long-term (i.e. >10 years) whole community fish dataincluding catch-per-unit-effort, abundance, biomass, andproduction from three lakes were used: 1) to examine variabilityin fish population and community measures among years using wholelake assessments of fish populations derived from mark recaptureexperiments, 2) to assess implications arising from monitoringindividual species vs. the whole fish community, and 3) toascertain whether, in fisheries assessments (science) a commonlyused surrogate measure, [catch-per-unit-effort (CPUE)] reflectedannual changes in the fish assemblage, and thus may be a goodestimator of abundance. High, long-term variability was evident in the abundance andbiomass of a fish species in our lakes, yet the communityremained relatively stable in terms of its biomass andproduction. Changes in total fish community biomass appear drivenby large species, which, relative to small fish species, remainstable among years. Among years, species richness remainedstable; however, fish species changed in the community. AnnualCPUE was found to be a suitable surrogate for abundance (N) ofsmall fishes; CPUE x mean weight of the catch (bCPUE) was asuitable surrogate for biomass (B) of large fishes. Prior toconcluding that a change in a fish population has occurred as aresult of a stressor, care must be taken to critically examinethe level of population assessment in order to avoid acceptingpotentially invalid conclusions.     

Picocyanobacteria – Sensitive Bioindicators of Contaminant Stress in an Alpine Lake (Traunsee Austria)

The abundance and photosynthetic activity ofpicocyanobacteria in the oligotrophic alpine lake Traunseewere measured at a station located close to the outlet ofindustrial soda waste and at a mid-lake reference stationduring spring, 1999 through to autumn, 2000.Picocyanobacterial numbers measured by flow cytometry inTraunsee (0.7–13.2 × 10⁴ ml^-1) were comparable tothose of other oligotrophic lakes, and there was nosignificant difference between the contaminated and thereference sampling location. Picoplankton (<2 m)photosynthetic rates measured in vitro by the ¹⁴C-technique were significantly reduced at the contaminated siterelative to the reference station at low photosyntheticallyavailable radiation (10 E m^-2 s^-1), while nodifference between these two stations was found at moderatelyhigh light intensity (100 E m^-2 s^-1). Theinvestigation was complemented by laboratory experiments withcultured picocyanobacteria. Three Synechococcus spp.strains were exposed to water taken from either of the twoTraunsee stations and from a control station located inneighbouring Attersee. Cell-specific photosynthetic activitymeasured by 4-h in vitro incubations revealed no significantdifference among the three stations investigated. Growthrates of the same three Synechococcus spp. strains weremeasured by flow cytometry over several days in thelaboratory. One strain, in particular, was sensitive to watertaken from the contaminated site; growth rate of this strainwas significantly reduced, relative to when exposed to watertaken from the reference station. Taken together, our resultsdemonstrate that picocyanobacteria are highly sensitivebioindicators of contaminant stress. The overall impact ofthe emissions from the industrial outlet on thepicocyanobacteria was, however, relatively minor.