Hypoxia in the Baltic Sea: Biogeochemical Cycles, Benthic Fauna, and Management

Hypoxia has occurred intermittently over the Holocene in the Baltic Sea, but the recent expansion from less than 10 000 km² before 1950 to >60 000 km² since 2000 is mainly caused by enhanced nutrient inputs from land and atmosphere. With worsening hypoxia, the role of sediments changes from nitrogen removal to nitrogen release as ammonium. At present, denitrification in the water column and sediments is equally important. Phosphorus is currently buried in sediments mainly in organic form, with an additional contribution of reduced Fe-phosphate minerals in the deep anoxic basins. Upon the transition to oxic conditions, a significant proportion of the organic phosphorus will be remineralized, with the phosphorus then being bound to iron oxides. This iron-oxide bound phosphorus is readily released to the water column upon the onset of hypoxia again. Important ecosystems services carried out by the benthic fauna, including biogeochemical feedback-loops and biomass production, are also lost with hypoxia. The results provide quantitative knowledge of nutrient release and recycling processes under various environmental conditions in support of decision support tools underlying the Baltic Sea Action Plan.     

乌鲁木齐市不同区域大气降尘中重金属污染及来源分析

为进一步了解城市不同区域间大气降尘中重金属含量及其差异性,沿城市走向梯度布设降尘采样点采集样品。采用电感耦合等离子体原子发射光谱(ICP-AES)仪测定样品中Cu、Cr、Mn、Fe、Ni、Zn、Cd、Pb和As等重金属含量,并计算富集因子来判断不同区域间的污染源类型,通过因子分析方法探讨污染的来源。结果显示,所测重金属元素中除Mn外,均受到人为源的影响,且十分严重。从贡献率来看,不同区域间第一因子的贡献率虽有差异,但均为来自土壤的风沙扬尘造成;第二因子的贡献率也不尽相同,主要是燃煤产生的污染;第三因子出现了差异,市南区和市北区主要是受金属冶炼的影响,而市中区的影响可能来自垃圾焚烧;市南区未出现第四因子,而市中区和市北区的污染源也不相同。分析表明,城市大气降尘污染依然严重,做好防控风沙和建筑扬尘,减少煤炭消耗,调整能源结构和产业布局是整体减少大气降尘的关键。     

Forest Die-Back Modified Plankton Recovery from Acidic Stress

We examined long-term data on water chemistry of Lake Rachelsee (Germany) following the changes in acidic depositions in central Europe since 1980s. Despite gradual chemical recovery of Rachelsee, its biological recovery was delayed. In 1999, lake recovery was abruptly reversed by a coincident forest die-back, which resulted in elevated terrestrial export of nitrate and ionic aluminum lasting ~5 years. This re-acidification episode provided unique opportunity to study plankton recovery in the rapidly recovering lake water after the abrupt decline in nitrate leaching from the catchment. There were sudden changes both in lake water chemistry and in plankton biomass structure, such as decreased bacterial filaments, increased phytoplankton biomass, and rotifer abundance. The shift from dominance of heterotrophic to autotrophic organisms suggested their substantial release from severe phosphorus stress. Such a rapid change in plankton structure in a lake recovering from acidity has, to the best of our knowledge, not been previously documented.     

Adsorption studies on coir pith for heavy metal removal

Biosorption efficiency of coir pith, a waste product from coir industry, was investigated in this study for the removal of metallic pollutants such as Ni, Cu and Zn from aqueous solutions. The disposal of coir pith is a major problem associated with the coir industries, especially working in the small-scale sector. The present study explores the effectiveness of utilization of coir pith, an accumulating waste, as a biosorbent for heavy metal removal. Batch mode studies were done to evaluate the efficiency of removal of metals under varying adsorption conditions of pH, metal concentration and contact time. Characterization studies of the biosorbent and SEM analysis were done. Kinetic modelling studies were tried using Lagergren pseudo-first-order and second-order models. Equilibrium studies were done using well-known Freundlich, Langmuir and D–R isotherm models. It was found that all isotherms are fitting well indicating the efficiency of coir pith as an adsorbent of heavy metals. The applicability of all the three isotherms to the sorption processes shows that both monolayer adsorption and heterogeneous energetic distribution of active sites on the surface of the adsorbent are possible. Due to the abundance and low cost of these materials, adsorption technologies developed can act as good sustainable options for the future in heavy metal removal from industrial effluents.     

Trace element content in soils of the King George and Elephant islands,maritime Antarctica

Trace element concentrations were studied in soils of the King George and Elephant islands in the maritime part of West Antarctica. The lowest concentrations of Cu, Pb, Cd, Zn, Ni and Mn were typical for the pristine soil of Elephant Island. The highest concentrations of these elements were found in the Fildes Peninsula and revealed the influence of human activities in the area of the Bellingshausen station and adjacent waste disposal sites. Ornithogenic soils of the Fildes Peninsula have shown low concentrations of Cd and As. Using geoaccumulation indexes, all the pristine soils of King George and Elephant islands and ornithogenic soils of the Fildes Peninsula were classified as unpolluted; the human-affected soils were mainly identified as moderately polluted. Obtained data can be used as background concentration levels for further researches.     

镍渣的重金属浸出特性

在分析镍渣的矿物相组成和重金属元素含量的基础上,鉴定了镍渣样品的浸出毒性,并考察了pH、液固比和浸出时间等条件对镍渣样中铬、铅、铜和锌等重金属浸出特性的影响。结果表明,镍渣中的重金属总量约为渣样的0.9%,且铬、铜和锌的含量较高,需进行安全管理。实验所用镍渣样品为第Ⅰ类一般工业固体废物。在强酸条件下镍渣中重金属浸出浓度较大,pH3后浸出浓度显著降低;液固比40 L/kg时,镍渣中重金属不断溶出,液固比40 L/kg后,浸出达到饱和,浸出浓度趋于平衡;随着浸出时间的增加,重金属离子的浸出浓度先增加后减少,但由于各重金属性质不同,各重金属达到最大浸出浓度的时间不同。     

南京市农用地土壤中重金属形态特征分析

以南京市农用地土壤为研究对象,采用顺序提取的方法对Cu、Zn、Pb、Cd做化学形态分析,了解不同元素各形态下空间赋存的含量与占比。结果表明,在农用地土壤中,上述4种金属元素所赋存的化学形态活泼性顺序为CdPbCuZn,其中Cd主要为醋酸提取态,Pb主要为可还原态,各占总量的40%以上,具有较高的生物有效性和潜在危害性;Cu与Zn主要为残渣态,占总量的60%左右,生物可利用性较低。由因子分析法可知,土壤p H值越大,Zn与Cd就越趋于向稳定的化学形态转化,土壤有机质含量越高,对Cu与Pb的络合能力就越强,可以降低其环境危害性。     

Characterisation of FOGs in grease trap waste from the processing of chickens in Thailand

Industrial firms that kill and process chickens generate wastewater that contains fat, oil, and grease (FOG). The FOGs are located in the fatty waste that is collected by floatation in grease traps. Chemical and physical characterisation of FOGs would provide useful information that would help in the development of methods designed to decrease the extent of pollution caused by disposal of the waste and to utilise commercially some of its lipid constituents. Employing these methods would enhance the profitability and competitive potential of these commercial organisations. Samples of grease trap waste from 14 firms in central Thailand have been examined. Due to the very different schemes of waste management employed by these firms, the physical appearance of their fatty wastes showed considerable variation. The chemical and physical properties of the FOGs present in these wastes showed considerable variation also. Large amounts of free fatty acids (10–70% as oleic acid) were detected in most of the 14 wastes and palmitic, cis-9-oleic, cis,cis-9,12-linoleic, stearic, and palmitoleic acids were the predominant species of free and esterified acids. Most of the FOGs were solid at temperatures below 40 °C. Many of them contained traces of heavy metals (Cu and Pb) and some contained traces of the pesticides dimethoate and cypermethrin. The content of these potentially hazardous substances would have to be considered very carefully before discarding the fatty wastes and during the development of methods designed to isolate their potentially profitable lipid constituents.     

SGA对垃圾焚烧飞灰中重金属的固化性能研究

根据EPA1311、HJ／T299—2007、HJ／T300—2007和HJ557—2009等国内外不同标准，研究了深圳某垃圾焚烧发电厂垃圾焚烧飞灰的浸出毒性，探讨了六硫代胍基甲酸（sixthioguanidineacid，SGA）、二甲基二硫代氨基甲酸盐（sodiumdimethyldithiocarbamate，SDD）和Ca（OH）2浓度对垃圾焚烧飞灰中重金属的固定性能的影响。研究结果表明，随着浸提液pH的降低，该厂焚烧飞灰中大部分金属元素的浸出量增大，焚烧飞灰浸出液中的cd、Ni、Ph和zn浓度分别超过国家危险废物鉴别标准（GB5085．3—2007）规定值的4．75倍、1．47倍、6．72倍和2．20倍，属于危险废弃物，必须进行稳定化处理。当固化剂SGA加入量为0．1mol／kg时，稳定化后的重金属浸出浓度已经低于危险废物鉴别标准，且对Cd、Cr、Cu和Pb的固化性能优于SDD和Ca（OH）2；当固化剂SGA、SDD和Ca（OH）2加入量为0．5mol／kg时，稳定化后的焚烧飞灰重金属浸出浓度均低于国家危险废物鉴别标准（GB5085．3-2007）中的规定值。与SDD和Ca（OH）：相比，SGA对垃圾焚烧飞灰中重金属的固化处理更具有优势。     

Bioaccumulation of trace elements in wild-growing edible mushrooms from Lubuskie voivodeship,Poland

Cu, Cr, Mn, Ni and Zn contents were quantified for three wild-growing edible species of macrofungi (Boletus edulis, Macrolepiota procera and Cantharellus cibarius) and underlying soil samples collected at forest sites in Lubuskie voivodeship, Poland. The total concentration of the analysed elements was determined using an ASA iCE 3000 series atomic absorption spectrometer. The analysis found significant differences in bioaccumulation between species and differing distributions of trace elements in the caps and stalks of fruiting bodies. Bioaccumulation factors revealed that Zn and Cu are the most bioaccumulated elements, whereas Cr and Mn are excluded from bioaccumulation. Macrolepiota procera showed the highest bioaccumulation of Cu, and Zn is accumulated to the greatest extent by Boletus edulis. A few significant differences (p≤0.05) between the examined species were observed.