South Pole Antarctica observations and modeling results: New insights on HOx radical and sulfur chemistry

Measurements of OH, H₂SO₄, and MSA at South Pole (SP) Antarctica were recorded as a part of the 2003 Antarctic Chemistry Investigation (ANTCI 2003). The time period 22 November, 2003–2 January, 2004 provided a unique opportunity to observe atmospheric chemistry at SP under both natural conditions as well as those uniquely defined by a solar eclipse event. Results under natural solar conditions generally confirmed those reported previously in the year 2000. In both years the major chemical driver leading to large scale fluctuations in OH was shifts in the concentration levels of NO. Like in 2000, however, the 2003 observational data were systematically lower than model predictions. This can be interpreted as indicating that the model mechanism is still missing a significant HO_x sink reaction(s); or, alternatively, that the OH calibration source may have problems. Still a final possibility could involve the integrity of the OH sampling scheme which involved a fixed building site. As expected, during the peak in the solar eclipse both NO and OH showed large decreases in their respective concentrations. Interestingly, the observational OH profile could only be approximated by the model mechanism upon adding an additional HO_x radical source in the form of snow emissions of CH₂O and/or H₂O₂. This would lead one to think that either CH₂O and/or H₂O₂ snow emissions represent a significant HO_x radical source under summertime conditions at SP. Observations of H₂SO₄ and MSA revealed both species to be present at very low concentrations (e.g., 5 × 10⁵ and 1 × 10⁵ molec cm^?3, respectively), but similar to those reported in 2000. The first measurements of SO₂ at SP demonstrated a close coupling with the oxidation product H₂SO₄. The observed low concentrations of MSA appear to be counter to the most recent thinking by glacio-chemists who have suggested that the plateau's lower atmosphere should have elevated levels of MSA. We speculate here that the absence of MSA may reflect efficient atmospheric removal mechanisms for this species involving either dynamical and/or chemical processes.     

Non-aromatic hydrocarbons in surface sediments near the Pearl River estuary in the South China Sea

Surface sediment samples at 4 sites along an offshore transect from outer continental shelf off the Pearl River estuary to the shelf slope region of the northern South China Sea, have been analyzed for total organic carbon (TOC), total nitrogen (TN), solvent extractable organic matter (EOM) and non-aromatic hydrocarbons. TOC, TN and EOM show distinct spatial variations. Their highest values are all recorded at the shelf slope region. EOM varies from 18.70-38.58 microgg(-1) dry sediment and accounts for 0.20-0.72% of the TOC contents. The non-aromatic hydrocarbons are an important fraction of EOM. Their contents range from 3.43-7.06 microgg(-1) dry sediment. n-Alkanes with carbon number ranging from 15-38 are identified. They derive from both biogenic and petrogenic sources in different proportions. Results of isoprenoid hydrocarbons, hopanes and steranes also suggest possible petroleum contamination.     

Economic growth,technology, and CO2 emissions in BRICS: Investigating the non-linear impacts of economic complexity

Environmental Science and Pollution Research - Upgrading economic structures and producing less pollution-intensive goods are indispensable for achieving Sustainable Development Goals (SDGs) in...     

贵州万山汞矿地区耐汞野生植物研究

在贵州万山地区废弃汞矿堆和矿山附近,受长期高剂量汞暴露的影响经过的自然选择,该地区出现了一些能耐受汞毒性的生态型植物。对汞耐受及汞富集植物的筛选对于汞污染土壤的植物修复具有一定的现实意义。通过对万山梅子溪地区汞污染土壤及汞耐受植物采样调查发现,该区域采样土壤中汞的含量均在50 mg·kg-1以上,达到重度汞污染水平。对该地区野生植物的采样分析发现,蔷薇科植物悬钩子不仅数量较多,单株植物生物量较大,表现出很强的耐汞毒性的能力,而且植株内可以很大程度地富集汞,在其植株中汞的含量可达20 mg·kg-1左右,属于汞富集植物,另外发现野蒿对汞也具有较强的富集能力,其植株中汞的含量可达10 mg·kg-1以上。该类型植物的发现将为植物的汞耐受以及汞富集机理研究提供新的素材,为汞污染土壤的植物修复技术提供新的植物类型,也为进一步开发汞污染土壤处理技术提供了一种可能。     

铝离子与聚硅酸的相互作用

本文应用核磁共振技术及化学分析方法研究了铝离子与聚硅酸之间的相互作用情况;借助于微电泳技术测定了含铝离子的聚硅酸絮凝剂在不同pH值条件下水解沉淀物的表面ζ电位变化情况;借助于透射电镜手段及静置观察方法考察了铝离子含量对聚硅酸胶凝作用的影响。实验结果表明,聚硅酸对铝离子具有一定的螯合(络合)和吸附作用,但二者之间不存在定量的作用关系,而是聚硅酸对铝离子的作用量随着铝离子含量的增加而增加。铝离子影响聚硅酸的胶凝时间,适量的铝离子的存在可延长聚硅酸的胶凝时间。聚硅酸的存在影响铝离子在不同pH值下的水解沉淀物的ζ电位值,使得达到零电位状态时的pH值向低pH值方向移动。     

Understanding the patterns and mechanisms of urban water ecosystem degradation: phytoplankton community structure and water quality in the Qinhuai River, Nanjing City, China

The temporal and spatial distribution characteristics of environmental parameters and the phytoplankton community were investigated in October 2010 and January 2011 in the Qinhuai River, Nanjing, China. Results showed that the water quality in the study area was generally poor, and the main parameters exceeding standards (level V) were nitrogen and phosphorus. The observed average concentrations of the total nitrogen (TN) were 4.90 mg?L^?1 in autumn and 9.29 mg?L^?1 in winter, and those of the total phosphorus (TP) were 0.24 mg?L^?1 in autumn and 0.88 mg?L^?1 in winter, respectively. Thirty-seven species, 30 genera, and four phyla of phytoplankton were detected in the river. Cyanophyta and Bacillariophyta were the dominant phyla in autumn, with average abundance and biomass of 221.5?×?10⁴?cells?L^?1 and 4.41 mg?L^?1, respectively. The dominant population in winter was Bacillariophyta, and the average abundance and biomass were 153.4?×?10⁴?cells?L^?1 and 6.58 mg?L^?1, respectively. The results of canonical correspondence analysis (CCA) between environmental parameters and phytoplankton communities showed that Chlorophyta could tolerate the higher concentrations of the permanganate index, nitrogen, and phosphorus in eutrophic water; Bacillariophyta could adapt well to changing water environments; and the TN/TP ratio had obvious impacts on the distributions of Cyanophyta, Euglenophyta, and some species of Chlorophyta. CCA analyses for autumn and winter data revealed that the main environmental parameters influencing phytoplankton distribution were water temperature, conductivity, and total nitrogen, and the secondary factors were dissolved oxygen, NH₄ ⁺–N, NO₃–N, TN, COD_Mn, TN/TP ratio, and oxidation-reduction potential.     

膜生物反应器处理苎麻脱胶废水的研究

利用膜生物反应器对苎麻生物脱胶废水进行试验研究,通过对废水中的COD、NH3-N、SS及色度进行检测发现,出水水质达到国家综合排放标准,并可回用。因此,此法处理麻生物脱胶废水可行,为苎麻生物脱胶废水的处理提供一种新的处理方法。     

不同模糊评价方法在水环境质量评价中的应用比较

近年来,运用模糊评价方法对水质和水体营养化程度进行评价逐渐受到重视。目前,对模糊评价方法的研究多集中在实测数据标准化、权重的确定和模糊模式识别模型研究几个方面。以滇池历年营养物质数据为实测数据,通过对几种实测数据标准化方法、权重确定方法和模糊模式识别方法的组合应用,获得水环境质量模糊评价最优组合方法。结果表明,在评价方法中,实测数据标准化方法采用线性内插法,权重的确定采用超标倍数法,模糊模式识别模型采用广义海明距离和加权海明距离法,即采用超标倍数法的广义海明距离和加权海明距离法能够更真实反映水环境质量的实际情况。     

同步辐射X射线荧光和吸收谱技术在环境汞污染研究中的应用进展

汞作为一种重要的全球性重金属污染物,被许多国际组织列为优先控制污染物。常规的汞分析手段,例如电感耦合等离子体质谱(ICP-MS)、原子荧光光谱(AFS)等,对汞的分析精度较高,方法比较成熟,但对样品前处理要求也较高。同步辐射技术由于其高、精、准的优势,且对样品前处理要求比较简单、可实现原位无损分析,因此被广泛应用于环境样品的分析中。随着研究的发展,同步辐射X射线荧光光谱(SRXRF)和同步辐射X射线吸收光谱(SRXAS)技术在环境汞污染分析领域得到了越来越多的应用。主要介绍了我国环境汞污染现状及污染特征,同步辐射技术对于汞分布蓄积、含量和化学形态分析方面的独特优势,重点回顾了本项目组和其他一些研究组近几年关于SRXRF和SRXAS技术在环境介质如土壤、植物体内汞的分布蓄积、相对含量和化学形态转化研究领域的应用进展,对进一步发展并提高同步辐射技术在环境及生物体汞污染水平、毒性机理和生态毒理评价方面的应用进行了展望。     

滨海滩涂不同围垦年代垦区农作物重金属累积特征及其与氮、磷的关系

为探明滨海滩涂围垦区农作物重金属累积特征及其与围垦年代、作物氮磷含量及化学计量比的关系,采集盐城地区不同围垦年代(围垦20、30、40、60年)农田4种主要作物(大麦、小麦、油菜、蚕豆)样品63个,测定了其根、茎叶和籽粒中Cd、Cu、Zn、Pb、Hg、As及全氮(N)、全磷(P)和粗蛋白(CP)含量,分析了重金属累积特征及与围垦年代、N、P、CP及N/P比的关系,并采用单因子污染指数法和内梅罗综合污染指数法对重金属污染程度和安全水平进行了评价。结果表明,1)围垦农田作物整株各指标含量分别为Cd (0.52±0.94)、Cu (12.98±16.00)、Zn (34.93±27.91)、Pb (3.50±5.88)、Hg (0.0063±0.0063)、As (1.94±3.72) mg·kg~(-1)及N(13.69±8.27)、P (5.98±2.24)、CP (79.55±49.54) g·kg~(-1);籽粒中则分别为(0.0059±0.020)、(1.83±1.48)、(11.13±4.45)、(0.09±0.30)、(0.0023±0.0036)、(0.0021±0.0048) mg·kg~(-1)及(19.21±7.68)、(6.04±1.64)、(111.78±47.81) g·kg~(-1); 2)作物重金属均表现为根茎叶籽粒,N和CP与之相反,表现为根茎叶籽粒,而P则表现为根籽粒茎叶; 3)不同围垦年代之间作物重金属、N、P、CP含量、N/P比及综合污染指数(Pz)均没有显著差异(P0.05); 4)各作物籽粒6种重金属单因子污染指数均值均小于1,除个别样品Pb超标(超标率11%)外,其他重金属均未超标; 5)作物籽粒重金属Pz均值为0.38,表明该地区作物重金属总体处于安全级,但大麦、小麦、油菜籽粒均有样品Pb含量超过警戒线,个别样品甚至达到重度污染水平; 6)作物整株各重金属之间、重金属与P之间均存在显著正相关(P0.01),而重金属与N、CP、N/P存在显著负相关(P0.01),在籽粒中则相关性均不显著(P0.05)。以上结果显示,盐城滨海滩涂围垦区作物重金属累积与围垦时间关系不大,其含量目前尚处于可接受范围内,但Pb污染值得关注,作物重金属与P之间存在一定的相互促进作用,而与N存在一定的拮抗作用,高氮低磷的机体养分状况有助于降低重金属含量。