铈异常及海水中铈的热力学

海相碳酸盐岩的铈异常可作为古海洋水氧化还原条件的一种指示剂。安哥拉海盐和巴西海盆(南大西洋)底部洋水在白垩纪时是还原环境,大约在54～58MaBP时,南大西洋变为类似于现在海水的氧化还原环境。本文提出了一个新的比较完善的铈氧化还原热力学公式,解释了长期悬而未决的海水和河水中铈地球化学异常的问题,如大西洋表层海水为何具有铈正异常等。查明于54～58MaBP非洲板块和南美板块彻底分离,统一的南、北大西洋开始形成。论证了阿尔卑斯运动和喜马拉雅运动是同步的。     

黄、东海海域水团发育对底质沉积物分布的影响

通过对黄、东海海域底质沉积物中的细粒级粘土矿物组合特征和全粒级碳酸盐含量分析、对比上覆水团和悬浮体资料，探讨研究区水团发育消长对底质沉积物分布的影响作用。结果表明研究区可以划分为长江冲淡水影响的长江型物质沉积区；黄海水影响的黄河型物质沉积区和黑潮水以及东海次表层水影响的残留型物质沉积区。而水团发育消长可直接影响下伏底质的分布特征。黄河型物质沉积区与残留型物质沉积区的分界相应于黄海冷水向东南扩展与黑潮次中层混合水向陆架爬升互为消长的长期综合平衡位置，而黄海冷水向东南的扩展范围代表着黄河物质在陆架向东南扩展沉积的最大范围．     

东海西湖凹陷保俶斜坡下第三系储层岩石学特征

东海西湖凹陷保俶斜坡下第三系储层砂岩为长石岩屑砂岩或岩屑长石砂岩，杂基含量小于5％，矿物成分主要为伊利石和绿泥石；胶结物主要成分为高岭石、石英次生加大边、碳酸盐矿物，总含量小于10％．     

四元体系Na~ ∥Cl~-,CO_3~(2-),B_4O_7~(2-)-H_2O 273K介稳相平衡研究

采用等温蒸发法研究简单四元体系Na ∥Cl-,CO32-,B4O72--H2O273K时的介稳相平衡,并测定该体系273K平衡液相中各组分的溶解度及密度,该体系的介稳相图和密度组成图显示:该四元体系在273K时的相图由3条溶解度单变量线、3个结晶区及1个共饱和点组成。体系属简单共饱型,无复盐或固溶体形成,3个结晶区分别对应单盐Na2CO3·10H2O,NaCl和Na2B4O7·10H2O。共饱点E处于Na2CO3·10H2O,NaCl及Na2B4O7·10H2O3盐共饱和,所对应的平衡液相组成为w(Na2CO3)=6.81%,w(NaCl)=21.69%,w(Na2B4O7)=0.65%,w(H2O)=70.85%。研究体系在273K下,Na2CO3·10H2O是碳酸钠盐的唯一析出形式,且硼酸钠对碳酸钠有盐析作用。     

Carbon and oxygen isotopic composition of car- bonate cements of different phases in terrigenous siliciclastic reservoirs and significance for their origin： A case study from sandstones of the Triassic Yanchang Formation, southwestern Ordos Basin, China

Early carbonate cements in the Yanchang Formation sandstones are composed mainly of calcite with relatively heavier carbon isotope （their δ^18O values range from -0.3‰- -0.1‰） and lighter oxygen isotope （their δ^18O values range from -22.1‰- -19.5‰）. Generally, they are closely related to the direct precipitation of oversaturated calcium carbonate from alkaline lake water. This kind of cementation plays an important role in enhancing the anti-compaction ability of sandstones, preserving intragranular volume and providing the mass basis for later disso- lution caused by acidic fluid flow to produce secondary porosity. Ferriferous calcites are characterized by relatively light carbon isotope with δ^13C values ranging from -8.02‰ to -3.23‰, and lighter oxygen isotope with δ^18O values ranging from -22.9‰ to -19.7‰, which is obviously related to the decarboxylation of organic matter during the late period of early diagenesis to the early period of late diagenesis. As the mid-late diagenetic products, ferriferous cal- cites in the study area are considered as the characteristic authigenic minerals for indicating large-scaled hydrocarbon influx and migration within the clastic reservoir. The late ankerite is relatively heavy in carbon isotope with δ^13C values ranging from -1.92‰ to -0.84‰, and shows a wide range of variations in oxygen isotopic composition, with δ^18O values ranging from -20.5‰ to -12.6‰. They are believed to have nothing to do with decarboxylation, but the previously formed marine carbonate rock fragments may serve as the chief carbon source for their precipitation, and the alkaline diagenetic environment at the mid-late stage would promote this process.     

δ^13C-δ^18O Covariance： An Effective Indicator of Hydrological Closure for Lakes？

The correlation between theδ~(13)C andδ~(18)O in primary carbonates is affected by several factors such as hydrological balance,total CO_2 concentrations,climatic condition and lake productivity. The influence of these factors on theδ~(13)C-δ~(18)O correlation may be different on different time scales.In this paper,two different-type lakes in southwestern China,Lake Erhai and Lake Chenghai,are selected to investigate the influence of climatic pattern on theδ~(13)C-δ~(18)O correlation and to evaluate the reliability of theδ~(13)C-δ~(18)O covariance as an indicator of hydrological closure.The results show that there exists good correlation between theδ~(13)C andδ~(18)O in Lake Erhai (overflowing open lake) and in Lake Chenghai (closed lake).This suggests that theδ~(13)C-δ~(18)O covariance may be not an effective indicator of hydrological closure for lakes,especially on short time scales.On the one hand,a hydrologically open lake may display covariantδ~(13)C andδ~(18)O as a result of climatic influence.The particular alternate warm-dry and cold-wet climatic pattern in southwestern China may be the principal cause of theδ~(13)C-δ~(18)O covariance in Lake Erhai and Lake Chenghai.On the other hand,a hydrologically closed lake unnecessarily displays covariant trends betweenδ~(13)C andδ~(18)O because of the buffering effect of high CO_2 concentration on theδ~(13)C shift in byper-alkaline lakes.We should be prudent when we use the covariance betweenδ~(13)C andδ~(18)O to judge the hydrological closure of lake.     

珲春中部土壤常量元素地球化学特征

采用XRF-X荧光光谱法,研究了吉林省珲春中部常量元素在表层土壤中的含量以及在土壤剖面中的迁移分布等土壤地球化学特征.结果表明:表层土壤中MgO(0.85%)、CaO(0.95%)的含量平均值低于全国土壤平均值(分别为1.8%和3.2%),Fe2O3(3.41%)、K2O(2.61%)、Al2O3(13.33%)、SiO2(69.25%)含量平均值与全国平均值基本相当(分别为3.40%,2.50%,12.60%和65.00%),Na2O(1.83%)含量平均值高于全国平均值(1.60%).暗棕壤和白浆土两种类型土壤剖面常量元素组成差别不大,在垂向上呈现出不同的规律性.Sa、Saf和ba指标反映出暗棕壤土壤的风化淋溶度略强于白浆土,在剖面不同层次上,随土壤深度的增加,Sa和Saf呈现下降的趋势,而表层土壤的ba值比深层土壤高.     

碳酸盐型磷矿的反浮选工艺研究

针对某碳酸盐型磷矿,采用反浮选工艺流程进行试验研究,获得了低镁优质磷精矿。反浮选工艺具有药剂种类少,分选效率高,选矿技术指标先进,操作控制容易等优点,是选别碳酸盐型磷矿的先进浮选工艺。     

滇西沘江流域水体中重金属元素的地球化学特征

通过测定流经兰坪金顸铅锌矿区的沘江水体中Pb、Zn、Cd、As的含量和底泥中重金属元素的化学形态的含量,分析了重金属元素的分布和化学形态的变化。结果表明,沘江水遭到了Cd污染,底泥已经成为重金属元素的蓄积库,以国家土壤环境质量标准（Ⅲ级）衡量,Pb、Zn、Cd和舡分别超标3．4倍、15．8倍、106倍和2．6倍。沘江水中重金属元素含量的峰值在矿山附近的下游,而底泥中重金属元素的峰值在矿山下游30-50km的地方,矿业活动、水流变缓、pH等水体环境条件的变化都能影响水和底泥中重金属元素的含量。底泥中的Pb以碳酸盐结合态为主,Zn和Cd以铁锰氧化物结合态为主,而As以残渣态为主。Pb、Cd、Zn三种元素的环境有效态含量比较高,对沘江流域生态环境具有潜在的巨大的危害。