FOREST HARVESTING AND STREAMWATER INORGANIC CHEMISTRY IN WESTERN NORTH AMERICA: A REVIEW1

The solution chemistry of forested streams primarily in western North America is explained by considering the major factors that influence this chemistry — geological weathering; atmospheric precipitation and climate; precipitation acidity; terrestrial biological processes; physical/chemical reactions in the soil; and physical, chemical, and biological processes within streams. Due to the complexity of all these processes and their varying importance for different chemicals, stream water chemistry has exhibited considerable geographic and temporal variation and is difficult to model accurately. The impacts of forest harvesting on stream water chemistry were reviewed by considering the effects of harvesting on each of the important factors controlling this chemistry, as well as other factors influencing these impacts ‐ extent of the watershed harvested, presence of buffer strips between streams and harvested areas, nature of post‐harvesting site preparation, revegetation rate following harvesting, pre‐harvesting soil fertility, and soil buffering capacity. These effects have sometimes reinforced one another but have sometimes been counterbalancing or slight so that harvesting impacts on stream water chemistry have been highly variable. Eight major knowledge gaps were identified, two of which — a scarcity of detailed stream chemical budgets and knowledge of longitudinal variation in stream chemistry — relate to undisturbed streams, while the remainder relate to forest harvesting effects.     

Quantum chemical investigation on photodegradation mechanisms of sulfamethoxypyridazine with dissolved inorganic matter and hydroxyl radical

Sulfamethoxypyridazine(SMP) is one of the commonly used sulfonamide antibiotics(SAs).SAs are mainly studied to undergo triplet-sensitized photodegradation in water under natural sunlight with other coexisting aquatic environmental organic pollutants.In this work,SMP was selected as a representative of SAs.We studied the mechanisms of triplet-sensitized photodegradation of SMP and the influence of selected dissolved inorganic matter,i.e.,anions(Br~-,Cl~-,and NO~-_3) and cations ions(Ca~(2+),Mg~(2+),and Zn~(2+)) on SMP photodegradation mechanism by quantum chemical methods.In addition,the degradation mechanisms of SMP by hydroxyl radical(OH·) were also investigated.The creation of SO_2 extrusion product was accessed with two different energy pathways(pathway-1 and pathway-2) by following two steps(step-I and step-II) in the tripletsensitized photodegradation of SMP.Due to low activation energy,the pathway-1 was considered as the main pathway to obtain SO_2 extrusion product.Step-II of pathway-1 was measured to be the rate-limiting step(RLS) of SMP photodegradation mechanism and the effect of the selected anions and cations was estimated for this step.All selected anions and cations promoted photodegradation of SMP by dropping the activation energy of pathway-1.The estimated low activation energies of different degradation pathways of SMP with OH·radical indicate that OH·radical is a very powerful oxidizing agent for SMP degradation via attack through benzene derivative and pyridazine derivative ring.     

中国村镇生活垃圾的养分与重金属含量特征及其农用潜力分析

对全国12个省份72个典型村镇进行了生活垃圾采样调查,系统分析了我国农村生活垃圾的基本理化特性、养分含量与重金属特征及其农用潜力。研究表明:我国典型村镇生活垃圾含水率为(53.68±8.84)%,p H为7.11±0.56,有机质含量为(49.04±10.49)%,C/N约为43∶1,C/P约为144∶1。除C/N略高外,其余特性均适合进行堆肥化处置。我国典型村镇生活垃圾中重金属As、Hg、Pb、Cd、Cr,Cu和Zn含量分别为(7.645±8.729),(0.737±0.480),(21.798±17.606),(3.356±11.012),(108.632±84.011),(36.834±10.905),(80.093±42.237)mg/kg。与国内相关标准相比,只有Hg、Cd超标,最大超标率分别为29.17%、43.75%;与欧美相关标准相比,仅有Cd、Cr超标,最大超标率分别为25.69%、37.50%。     

区域空气质量模拟中查表法的应用研究

在自行开发完善的区域空气质量模式系统RegSRRMS中应用查表法,模拟中国典型城市群对流层大气主要污染物的浓度变化,评估该方法在大气复合污染事件预测和控制中的有效性.首先,利用具有国际先进水平的空气质量模式WRF-CHEM中的化学模块建立了包含完善气相化学、气溶胶过程的箱模式WRFBOX.其次,利用WRFBOX进行化学反应敏感性分析,基于影响污染物的重要因子分别建立了臭氧(O3)及其前体物、无机盐气溶胶和二次有机气溶胶(SOA)查算表数据库,并检验其有效性.最后,将此查算表数据库引入RegSRRMS,建立简化的查表算法.利用直接耦合机制法和查表法对2000年3月珠三角地区污染个例中主要大气污染物浓度进行模拟.通过比较2种方法的模拟结果,显示查表法计算效率提高了57%,能够反映大气光化学反应的非线性特征、气溶胶及其前体物的平衡关系,具有高分辨率、高时效性,能够方便快捷地给出源和受体之间的响应关系,结果可靠.在区域空气质量模式中应用查表法有利于大气污染事件的快速预测以及大气污染控制的快速决策.     

云贵高原湖区湖泊营养物生态分区技术方法研究

提出一种基于主成分分析、聚类分析、判别分析和空间自相关的分区模型,用于对云贵高原湖区湖泊营养物生态分区的研究.首先运用主成分分析方法对众多指标进行了降维综合处理,产生彼此互补相关又能综合反映湖区情况的4个新指标,累计贡献率达到93.69%,具有充分的代表性,构建了云贵高原湖区湖泊营养物生态分区指标体系.在此基础上,根据各区域新指标值,结合聚类模型初步将湖泊流域分为5类,再利用判别分析完成非湖泊流域的类别判别,最后运用空间自相关分析方法,按聚类结果进行全局自相关分析,Moran’sI为0.320,且检验值Z值为68.2,远大于临界值(显著水平1%所对应的临界值2.58),表明聚类结果与空间位置具有显著相关性,之后运用局部自相关对区域各因素的主成分综合得分的空间分布格局进行了量化分析,揭示了零散分类区块在空间地域分布上的关联和差异,根据关联结果完成最终的分区.结果表明,利用此分区模型可以尽量避免人为因素,得到更为客观的分区结果,具有良好的适应性和可行性,可为探索适合我国湖泊营养物生态分区的指标体系和分区技术方法,完成全国湖泊营养物生态分区和科学地制定我国湖泊营养物基准和富营养化控制标准提供技术支持.     

Ionic composition of submicron particles (PM1.0) during the long-lasting haze period in January 2013 in Wuhan, central China

In January 2013, a long-lasting severe haze episode occurred in Northern and Central China; at its maximum, it covered a land area of approximately 1.4 million km². In Wuhan, the largest city in Central China, this event was the most severe haze episode in the 21st century. Aerosol samples of submicron particles (PM_1.0) were collected during the long-lasting haze episode at an urban site and a suburban site in Wuhan to investigate the ion characteristics of PM_1.0 in this area. The mass concentrations of PM_1.0 and its water-soluble inorganic ions (WSIIs) were almost at the same levels at two sites, which indicates that PM_1.0 pollution occurs on a regional scale in Wuhan. WSIIs (Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺, Cl^-, NO₃^- and SO₄^2-) were the dominant chemical species and constituted up to 48.4% and 47.4% of PM_1.0 at WD and TH, respectively. The concentrations of PM_1.0 and WSIIs on haze days were approximately two times higher than on normal days. The ion balance calculations indicate that the particles were more acidic on haze days than on normal days. The results of the back trajectory analysis imply that the high concentrations of PM_1.0 and its water-soluble inorganic ions may be caused by stagnant weather conditions in Wuhan.     

重金属抗性解磷细菌的磷溶解特性研究

从湖南省湘西州花垣县的铅锌矿表层土壤中,筛选出两株具有重金属抗性和解磷特性的细菌T PSB1和T PSB2.通过16S rRNA基因序列比对,分别鉴定为嗜麦芽寡养单胞菌(Stenotrophomonas maltophilia)和唐菖蒲伯克霍尔德菌(Burkholderia gladioli).T PSB1和T PSB2在含有难溶性无机磷液体培养基中,其上清液的可溶性磷含量最高分别达到了402.9 mg·L-1和589.9 mg·L-1;在难溶性有机磷固体和液体培养基中,固体平板上均出现解磷圈,而液体培养基上清液中,可溶性磷含量也分别达到了2.97 mg·L-1和4.69 mg·L-1.另外,两株细菌对重金属Zn2+的抗性最高,在其浓度为2000 mg·L-1固体和液体培养基条件下均可以生长,磷溶解浓度分别为114.8 mg·L-1和125.1 mg·L-1.而在含铬和铅的浓度为1 000 mg·L-1的液体培养基中,两株细菌同样表现出重金属抗性.在Pb2+浓度为1000 mg·L-1的液体培养基中,磷溶解浓度分别达到了57.9 mg·L-1和71.7 mg·L-1;而在Cr2+浓度为1000 mg·L-1的培养基中磷溶解浓度分别为60.1 mg·L-1和98.4 mg·L-1.     

东莞市大气亚微米粒子PM1及其中水溶性无机离子的污染特征

2011年8月—2012年7月期间,利用中流量(100 L·min-1)大气采样器对东莞市A和B两点(A:生活区,B:工业区)进行PM1、PM1~2.5、PM2.5~10采样,并定量分析颗粒物上F-、Cl-、NO-3、SO2-4、NH+4、Na+、K+、Ca2+、Mg2+等9种水溶性无机离子.分析结果显示,工业区B点的细粒子污染较生活区A点严重,B点PM1质量浓度年均值为48μg·m-3,其浓度是A点的1.2倍.A、B两点PM1对PM2.5和PM10的质量贡献率无明显差异,平均贡献率分别高达69%和45%.二次离子SO2-4、NO-3、NH+4及与燃烧行为有关的K+、Cl-等5种离子在细粒子PM1上富集,这5种离子对PM1质量的贡献率分别为18.82%~19.76%、4.98%~5.47%、3.98%~4.12%、2.03%~2.27%和3.39%~3.78%.而其他4种离子,Ca2+、Mg2+、F-和Na+积聚在粗粒子PM2.5~10上.PM10/PM2.5/PM1三种粒子中,PM1粒子酸性值AE/CE(阴离子当量浓度/阳离子当量浓度)比值和硫转化率SOR、氮转化率NOR值均是最高.     

优势微生物菌群消减有机污泥作用效果分析

本文阐述用优势微生物菌群消解有机污泥的作用效果及原因,指出了优势菌群的构成类别和消解特点。实验结果表明,污泥消解率可达到55%,且过程对出水水质不产生负面影响,水质指标均符合GB18918-2002要求。     

海州湾海洋牧场人工鱼礁投放对营养盐的影响

为了解海州湾海洋牧场人工鱼礁投放对营养盐的影响,基于2008—2015年间共24个航次水质调查资料,分析了海州湾海洋牧场鱼礁区和对照区活性磷酸盐(PO_4~(3-)-P)、活性硅酸盐(SiO_3~(2-)-Si)和溶解无机氮(DIN)的浓度、组成及营养盐结构的变化.同时,比较了鱼礁区和对照区营养盐的变化,初步分析了人工鱼礁投放量与营养盐的相关性,尝试探索人工鱼礁投放对营养盐浓度与结构的影响.结果表明,鱼礁区和对照区PO_4~(3-)-P、SiO_3~(2-)-Si浓度均呈现出秋季夏季春季的特点,且鱼礁区高于对照区.DIN在鱼礁区和对照区也呈现出同样的季节变化特点,但鱼礁区的变化幅度显著大于对照区.海洋牧场人工鱼礁的投放使鱼礁区PO_4~(3-)-P和DIN浓度增加.受热力学平衡的影响,对照区DIN浓度也出现了增加,而PO_4~(3-)-P受人工鱼礁投放的影响小.鱼礁区和对照区SiO_3~(2-)-Si受人工鱼礁投放影响均不明显.另外,海洋牧场DIN组成也发生了改变,2012年前NO_3~--N为DIN主要组成,之后为NH_4~+-N.营养盐结构分析显示,海州湾海洋牧场营养盐对浮游植物主要表现为磷限制.