Possibility of degradation of phenylarsonic acid in the presence of ferrihydrite

Although inorganic species are predominant in natural systems, but there are many kinds of organoarsenic species such as methylated and phenylated arsenic compounds. Phenylarsonic acid （PA） is a degradation product of organoarsenics used for chemical warfare agents, which has been detected in well water at the disposal site of the agents in Japan. There are few reports studying behavior of PA in soil. In this study, PA was adsorbed onto ferrihydrite and its chemical forms were determined using high performance liquid chromatography connected to inductivity-coupled plasma mass spectrometry （HPLC-ICP-MS）. 100 mg/kg of PA was mixed with 0.03 g of 2-line ferrihydrite. For each suspension, pH was adjusted by HNO3 or NaOH. Each sample was incubated for more than 19 hours and the final pH was measured. After filtration, the chemical form of arsenic in the filtrate was measured using HPLC-ICP-MS. In addition, ferrihydrite separated by filtration was dissolved by 3 ml of 0.5 M HCI and the arsenic species in the solution was detected by HPLC-ICP-MS （column： Tosoh TSKgel SuperlC-AP, eluent： 0.01 M HNO3）. It was verified that PA is not degraded by heating in 0.5 M HCl solution. At pH 3.1, any arsenic compounds were not detected from the solution, because almost all arsenic species were adsorbed onto ferrihydrite at lower pH. At pH= 12, however, 7%-10% of inorganic arsenic was detected in the solution. In solid phase, there are some problems to determine the precise ratio of inorganic and organic species. When the solution includes Fe ion at 0.01 M level, the retention time of arsenic species drifted compared to those in standard solution, which makes it difficult to determine precisely the arsenic species adsorbed on ferrihydrite. Therefore, more study is needed to determine the ratio of inorganic and organic species in the system.     

Occurrence of microorganic pollutants in the atmosphere of Singapore during haze and non-haze periods

Microorganic pollutants such as polycylic aromatic hydrocarbons （PAHs）, organochlorine pesticides （OCPs）, polychlorinated biphenyls （PCBs） and total petroleum hydrocarbons （TPHs） are known to be present in urban ambient air. These organic compounds are prone to atmospheric transport and deposition over long distances, thus enabling them to accumulate even in regions remote from their sources. Deposition from the atmosphere can be via direct deposition and exchange with crops that may be directly or indirectly ingested by humans. It can also take place via wet and dry deposition and air-water exchange. Following their deposition, these microorganic pollutants tend to accumulate in soils, sediments and in human and ecological food chains. There are many reports in the literature on the atmospheric concentrations of microorganic pollutants, but there are few reports and data in Asia. This study was performed in Singapore to determine the relative amounts of persistent organic pollutants and TPHs in ambient aerosols. One of the important sources of these organic compounds in Southeast Asia is thought to be biomass burning （vegetation fires）. Hence, air sampling was conducted during both smoke haze and non-haze periods. The data obtained from this study will be presented and discussed.     

电吸附找矿法在捕获常规化探方法难以发现的异常时的有效性

电吸附找矿法是一种针对寻找隐伏矿而研制的找矿新方法,它属金属活动态提取法的一种,其找矿原理是:深埋藏隐伏矿在地电化学作用下发生溶解,溶解出来的矿物质在各种迁移动力的驱动下,从地下深部向上运移到地表,进入土壤形成后生异常.后生异常组分多属活动态,但活动态组分不仅存在于后生异常中,也存在于同生异常--原生晕异常和次生晕异常中,因此,应用电吸附找矿法寻找露头矿和浅埋藏矿时,其效果与常规化探方法是一样的;但电吸附找矿法的主要作用是可应用于寻找深埋藏隐伏矿,因由隐伏矿引起的后生异常活动态组分含量很低,常规化探方法很难发现它,而电吸附找矿法却能捕获它.     

梁子湖水体P的季节变化与沉积物P释放初步研究

采用分级测定的方法对梁子湖沉积物中无机磷酸盐进行了分析,测定了梁子湖水体P的季节变化,并以室内模拟的方法研究梁子湖沉积物在pH值和温度控制下P的释放特征。研究表明,梁子湖水体P的含量呈明显的季节变化,冬季高,夏季低。沉积物无机磷(P i)中以钙磷(Ca—P)为主(55%~61%),铁磷(Fe—P)次之(28%~33%),铝磷(A l—P)最少(3%~5%)。在梁子湖的入水口和出水口,由于沉积环境影响到P的形态,P的释放明显较湖心高。在试验初期,由于扰动的影响,使得P的释放在第1天比第2天和第3天高,其后P的释放量则迅速增加。温度对P释放影响明显,其具体表现为,30℃时P释放达到峰值的时间比4℃时提前4 d,而且前者峰值比后者高出9倍。pH值对沉积物P释放同样有明显的影响,与正常状态下的湖水条件(pH值为8.5)相比,偏酸(pH值为5.5)和偏碱(pH值为11.5)条件下,P的释放量增加。     

Origin and three-dimensional fluorescence spectrum of the chromophoric dissolved organic matter in Yangtze estuary, East China

Dissolved organic matter （DOM） is an important chemical component in natural water. Chromophoric dissolved organic matter （CDOM）, a fraction of optical properties, plays art important role in the biogeochemical cycle of nutrients in aquatic environment. People realized that DOM cycle is crucial in the global carbon and nitrogen flux, and also is inherently related to nutrients and trace metal elements. Therefore, CDOM was concerned by scientists in global oceanography and limnology fields. Water samples were collected from three sections （North Channel, South Channel and Zhuyuan） of the Yangtze （Changjiang River） estuary in March 2006 Three-dimensional excitation emission matrix （3-DEEM） fluorescence spectra were analyzed for those filtrates through Whatman GF/F filters. Dissolved organic carbon （DOC） was also measured by TOC analyzer. The tidal variety was also taken into account. The 3-D EEM fluorescence scans suggested the fluorescence characteristics of humic acid （Ex=332-344 nm, Em=439-451 nm） and fulvic acid （Ex=250-254 nm, Em=472-478 nm） were obvious, and the fluorescence group of protein-like and tyrosine （Ex=230 nm, Em=283 nm） was also found. They are mainly composed of CDOM in the Yangtze estuary. Further data analysis, especially the fluorescence index （f 450/500）, showed that terrestrial signal was rather strong （1.41-1.65） in the surface water, however, some terrestrial CDOM signals of bottom water showed excursions （1.28-1.39）. On the other hand, anthropogenic sign was impressed in the waters of Zhuyuan, which is one of the main drain outlets of Shanghai Metropolis. DOC concentrations ranged from 2.2 mg/L to 3.4 mg/L in Zhuyuan and South Channel, and from 2.0 mg/L to 2.4 mg/L in North Channel. The tide effect played a role in the composition of the CDOM measured by 3-D fluorescence scan technology.     

Water chemical behavior at Yangtze （Changjiang） River estuary

Geochemical cycling has received wide attention due to the need to understand the pathways of pollutants through our present environment. In this regard the Yangtze River plays a significant role in putting those pollutants into the East China SeafWorld Oceans. The Yangtze River is of high sedimentation rate and water discharge. The watershed covers variable climate regions from temperate to subtropical and from semiarid to humid. Twenty three （23） sampling locations at the estuary have been selected for understanding the dynamic relationships. The elements （Cl^-, SO4^2-, Na^＋, K^＋, and Ca^2＋） show conservative behavior during mixing of fresh water with saline water whereas Mg^2＋, Mn^2＋ show a non-conservative pattern . The relationships between Na^＋/SO4^2- and Cl^-/SO4^2- molar ratios show a mixing of more than two water sources.     

湿地生态系统碳循环过程及碳动态模型

从地上、地下有机物质生产对湿地碳输入的贡献,湿地土壤碳库以及土地利用变化对湿地土壤碳库和碳排放的影响,甲烷排放和可溶性有机碳输出以及影响因子,湿地生态系统碳循环动态模型4个方面对湿地生态系统碳循环国内外研究进展和研究成果进行综述、分析,提出了我国亚热带区域天然湿地碳循环研究的主要热点和方向:⑴沿海湿地碳库估算及土地利用转化对土壤碳库和温室气体排放的影响;⑵酸沉降对于我国东南沿海低纬度地区湿地甲烷排放的影响;⑶沿海湿地生态系统碳循环动态模型的应用与开发;⑷湿地系统可溶性有机碳的输出机理探讨.     

库车坳陷侏罗系煤成气动力学模拟研究

应用黄金管—高压釜封闭体系热模拟实验与GC、GC-IRMS分析技术,结合KINETICS专用软件,对库车坳陷侏罗系煤成气进行了动力学模拟研究。库车坳陷侏罗系煤具有高的产气性,在高演化阶段主要产甲烷气;侏罗系煤热解气甲烷碳同位素为-36‰～-25‰,乙烷碳同位素为-28‰～-16‰;甲烷、C2-C5气态烃的生成活化能分别为(47～64k)calm/ol、(55～72k)calm/ol,频率因子各为5.265×1013s-1、5.388×1018s-1。在此基础上,进一步探讨了克拉2气田天然气的成因。研究认为,克拉2气田天然气属阶段捕获的煤成气,主要聚集了5～1Ma时期的天然气,其成熟度Ro分布范围为1.3%～2.5%。