黄土高原和南海陆架古季风演变的生物记录与Heinrich事件

宝鸡黄土中０．１５Ｍａ以来植物硅酸体研究表明,年均温度、１月份和年均降水量的变化与深海氧同位素变化有很好的一致性,而７月份降水量的变化与印度洋反映季风强弱的粒度变化相类似。南海陆架孢粉研究发现,１４７００—１３９００ａＢ．Ｐ．和２２９００一２０６００ａＢ．Ｐ．气候变冷期与北大西洋沉积物中Ｈ１、Ｈ２变冷事件存在成因上的联系。全球冰量通过冬季风等因素在“轨道尺度”上可能影响了夏季风对特定地区的控制时间,从而控制了黄土区气候的年均状况,但没有影响夏季风固有的变化周期和振幅。由低纬夏季太阳辐射控制的夏季风以其准２００００ａ周期叠加在冬季风所具有的准０．１Ｍａ周期上。冬、夏季风的演化行为具有较强的相对独立性,冬、夏季风同时减弱或增强的情况是存在的。Ｈｅｉｎｒｉｃｈ事件在东亚地区不仅影响了冬季风而且影响了夏季风。     

扬子地台前寒武纪－寒武纪界线地层的微体植物化石群

前寒武纪一寒武纪界线地层在扬子地台发育良好、分布广泛,并有包括微体植物群、海藻、瓶形原生物、具硬体动物及‘澄江动物群’等化石的发现。因而,扬子地台成为研究前寒武纪－寒武纪界线生物地层的代表地区之一。基于对扬子地台前寒武纪－寒武纪界线地层已知微体植物化石记录的回顾和论定,总结概括了下寒武统微体植物化石组合：寒武系最底部硅质磷块岩中的Ｍｉｃｒｈｙｓｔｒｉｄｉｕｍ－Ｐａｒａｃｙｍａｔｉｏｓｐｈａｅｒａ－Ｍｅｇａｔｈｒｉｘ组合和较高层位页岩的Ｓｋｉａｇｉａ－Ａｎｎｕｌｕｍ－Ａｒｃｈａｅｏｄｉｓｃｉｎａ组合。它们分别与Ａｎａｂａｒｉｔｅｓ－Ｃｉｒｃｏｔｈｅｃａ－Ｐｒｏｔｏｈｅｒｔｚｉｎａ小壳动物化石带和Ｐａｒａｂａｄｉｅｌｌａ及Ｅｏｒｅｄｌｉｃｈｉａ三叶虫带相对应。与东欧地台疑源类生物地层相对照,扬子地台Ｍｉｃｒｈｙｓｔｒｉｄｉｕｍ－Ｐａｒａｃｙｍａｔｉｏｓｐｈａｅｒａ－Ｍｅｇａｔｈｒｉｘ组合的纵向分布大体和东欧地台Ａｓｔｅｒｉｄｉｕｍｔｏｒｎａｔｕｍ－Ｃｏｍａｓｐｈａｅｒｉｄｉｕｍｖｅｌｖｅｔｕｍ组合带相一致,而以上两地台的化石组合产出层位可能都略高于纽芬兰东部剖面,依据Ｐｈｙｃｏｄｅｓｐｅｄｕｍ所厘定的寒武系底界?     

冀西北长城纪宣龙式铁矿层中微体植物化石的发现及其意义

本文研究的是笔者等在冀西北长城系串岭沟组宣龙式铁矿层中发现的微体植物化石,这些化石都保存在铁质叠层石(肾状赤铁矿)和铁质核形石(鲕状赤铁矿)的基本层中。微化石以丝状体为主,部分为球状体。归属于原核生物蓝藻门颤藻科的两个属和色球藻科的一个属。化石层同位素年龄约在1800—1757Ma。这些化石与北美冈弗林特组微化石比较,既有些相似,又有些区别。该化石的发现为研究铁矿的成因,指示沉积环境及层位对比都很有意义。     

岩溶区集中式饮用水源地水质评价与保护——以毕节市倒天河水库和利民水库为例

采用SPSS软件，对2003年01月至2004年12月期间，倒天河水库和利民水库逐月水质监测数据进行数理统计分析，结果表明毕节市饮用水水质污染有较明显的季节变化和空间差异；且不同污染物对水体污染的贡献率各不相同，总磷和粪大肠菌群所占份额最大，方差累积贡献率达77％。在此基础上，利用加权综合污染指数对水体水质污染现状进行综合评价，结果显示倒天河水库和利民水库，水质污染总体较轻．饮用水水质符合《地表水环境质量标准（GB3838—2002）》中Ⅲ类水质标准；最后提出加大水环境保护的建议。     

论四川盆地三叠系地下水水文地质条件

四川盆地三叠系地下水可划分出碎屑岩孔隙裂隙和碳酸盐岩岩溶裂隙两大储集类型。按此处构造开启程度和埋深条件等的不同,下中三叠统地下水有沉积变质水和渗入淋滤水两种基本成因类型,水动力特征各异。沉积变质水处于深埋封闭条件,受地静压力驱动控制;渗入淋滤水分布于背斜露头区和浅部地区,受静水压力驱动控制。并由此控制了盆地三叠系盐类的保存条件。     

安徽铜陵凤凰山铜（金）矿床矽卡岩型与斑岩型复合成矿作用流体研究

凤凰山铜（金）矿床产于燕山晚期花岗闪长岩及石英二长闪长斑岩与三叠系碳酸盐岩的接触带，先后包括矽卡岩型和斑岩型两期矿化，并可细分为9个成矿阶段。矿石中广泛出现角砾状和细脉状、网脉状构造。流体包裹体特征及显微冷热台测温资料表明，成矿流体存在过沸腾和局部超高压等现象。两个成矿期都经历了从高温高盐度向低温低盐度的转变，成矿溶液的主要成分也由钾钠型变成了钠钙型。来源于岩浆热液的早期含矿流体与来自围岩的地下水热液的混合可以解释成矿流体的这种演化。     

陕西省水工程勘察规划研究院

陕西省水工程勘察规划研究院始建于一九四九年。长期以来承担着全省地下水监测研究、地下水盗源调查评价、地下水开发利用规划、钻井技术设备研究、科技推广等专业按术工作和机井工程建设监督、质量管理，钻井施工资质管理等行业技术管理工作。具有国家甲级水文水资源调查评价、建设项目水资源论证、水文地质勘察、岩土工程资质．     

Mobility of heavy metals from tailings to stream waters in local zinc smelting activities contaminated site

It has been found that stream waters were severely contaminated with wastes from a long-time smelting factory in Hezhang, Guizhou, China. The main sources of contamination are the smelting wastes stored in the open air and abandoned in the vicinity of stream. A method of lead isotope was adopted in order to identify relations between tailings and water contamination. Representative samples of tailings and stream sediments were collected. Mineralogical characterizations were conducted using XRD and TEM/SEM, while acid digestion was carried out for determining metal contents. BCR sequential leaching tests were performed in order to assess metal mobility. The tremendous ‘actual＇ and ‘potential＇ mobility of heavy metals indicates that the smelting waste and stream sediments present a considerable threat to the environment. Besides the chemical remobilization of heavy metals from the sediments and the reworking of riverbed sediments act as a secondary source of pollution. Also groundwater and stream water were sampled in specific locations and were measured.     

Geochemistry of porewater and sulfate-reducing bacteria in sediment cores from the Chianan Plain, Taiwan

High concentrations of arsenic and humic substances in groundwater from the southwestern coastal plain of Taiwan were well known for their probable relationships with black-foot disease. In order to realize the relationships between the concentrations of humic substances and arsenic in this area, 24 well water samples were analyzed. After filtered through 0.45 μm glass fiber membrane in the field, samples were kept in the dark at 4℃ and then separated into six fractions with varying range of molecular weight （〈0.5, 0.5-1, 1-5, 5-10, 10-50 and 〉50 k Da） by ultrafiltration apparatus （Molecular/Por Stirred Cell system） in the lab. Concentrations of humic substances were measured by fluorescence spectrometer （HITACHI F-2000, ex=370, em=445） and arsenic by FIAS-AA （Perkin Elmer AAnalyst 100, FIAS-400）. On average, only 6.2% of the total arsenic in water existed in the fraction of 〉0.5 k Da. and the others were complexed with humic substances （including humic acid and fulvic acid）. The results demonstrated a distinct positive correlation between the concentrations of humic substances and arsenic.     

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.