广东三水盆地古近系心组生油层的元素地球化学特征

沉积物的元素地球化学特征是对沉积盆地水体环境以及古气候条件变化的响应。本文根据元素（Al、Fe、Mg、Ca、K、Na、P、V、Ni、Co、Cr、Cu、Zn、Sr、Ba、Cd、Li、Mn、Pb、Ti）的含量及其比值（Al/Ti、Fe/Mn、Sr/Ba、Mg/Ca、Sr/Ca、Na/Ca、V/Cr、Ni/Co、Ni/V）的变化，对三水盆地古近系心组红岗段生油层的沉积条件进行了系统分析。心组红岗段下部（亚段A）表现为较稳定的地球化学特征。各元素丰度及其比值指示这一时期陆源输入持续较高、且物源组成变化不大。由于海水入侵的影响，湖盆水体盐度相对较高，底部水体以弱氧化条件为主，O₂-H₂S界面位于水/沉积物界面附近。红岗段中上部（亚段B、C）的元素地球化学特征变化较为频繁且幅度很大，反映古气候和湖盆沉积条件的迅速变迁。在潮湿气候条件下，沉积物的地球化学特征表现为以Al、Ti为代表的外源元素含量及其比值较高，而Mg、Ca等盆内化学沉积元素含量较低。古氧气指标指示底部水体为还原环境，有利于有机质保存。因而，相应于较高的有机碳含量。在间歇性干旱时期，陆源输入减少，外源元素含量及其比值显著降低。随着蒸发作用的加强，水体盐度加大，内源元素丰度以及Mg/Ca、Sr/Ba、Sr/Ca和Na/Ca比值大幅度上升。底部水体为氧化环境，O₂-H₂S界面多位于水/沉积物界面或沉积物中。上述两种气候条件在红岗段中上部沉积时期交替出现。红岗段沉积后期由于淡水的长期输入，湖水出现逐渐淡化趋势。     

豫西鸡冠洞洞穴水及现代沉积物Mg, Sr和Ba记录及其意义

采用电感耦合等离子体质谱仪（ICP-MS）和电感耦合等离子体光谱仪（ICP-OES）对2009年12月-2013年8月采自河南省栾川县鸡冠洞洞穴水（滴水、池水及地下河水）和现代碳酸盐沉积物的 Ca、Mg、Sr和 Ba 微量元素地球化学指标进行了分析。结果显示：（1）鸡冠洞洞穴水的 Mg/Ca对地表环境的干湿条件变化响应迅速,具体表现为池水和地下河水 Mg/Ca旱季高而雨季低,而 Sr/Ca 和Ba/Ca的变化与降水和气温的关系并不明显;（2）鸡冠洞现代沉积物的 Mg/Ca 变化与滴水有着良好的对应关系,但现代沉积物的 Sr/Ca和 Ba/Ca可能受大气粉尘活动和地表土壤的影响,变化趋势与 Mg/Ca 相反;（3）鸡冠洞碳酸盐岩与岩溶水间 Sr/Ca和 Mg/Ca的分配系数KSr值在0.02-0.18之间,KMg值在0.01-0.03之间,KMg值与洞穴温度的正相关关系不明显。     

南海北部琼东南海域HQ-48PC站位地球化学特征及对天然气水合物的指示意义

南海北部陆坡琼东南海域是中国天然气水合物勘探最具潜力的区域之一。对该海域的HQ-48PC站位沉积物样品的顶空气甲烷含量、孔隙水阴、阳离子及微量元素含量等地球化学特征进行综合分析,结果显示:在硫酸盐-甲烷界面(SMI,Sulfate-Methane Interface)(推算深度约为6.05 mbsf)发生了强烈的甲烷厌氧氧化反应(AMO,Anaerobic Meth-ane Oxidation),主要表现为SO24-含量线性降低接近于0、CH4含量发生骤增、有机碳和黄铁矿含量达到最大值及形成一个"钡锋"等特征。在SMI之上,HCO3-浓度随深度的增加呈明显上升的趋势,Ca2+、Mg2+、Sr2+等离子浓度随深度的增加呈降低的趋势,Mg2+/Ca2+比值随深度的增加呈明显增加的趋势,自生碳酸盐矿物以方解石为主;在SMI之下,HCO3-浓度随深度的增加呈缓慢下降的趋势,Ca2+浓度变化不大,Mg2+、Sr2+浓度和Mg2+/Ca2+比值随深度的增加呈降低的趋势,自生碳酸盐矿物以白云石为主。沉积物孔隙水的PO34-和NH4+含量较高,它们随深度的增加呈明显升高的趋势,且这种变化趋势与SO42-含量的下降趋势大致呈镜像关系。这些地球化学异常特征与国际上已发现有天然气水合物地区的地球化学特征相类似,暗示该采样站位深部沉积物中可能赋存有天然气水合物藏。     

东营凹陷古近系中深层湖盆演化中的无机元素响应

为查明无机元素分布与水深、盐度等沉积环境以及湖盆演化过程的关系,采用电感耦合等离子体发射光谱仪分析对东营凹陷郝科1科探井古近系深层微量元素含量进行了测试、分析,所涉及的研究层位是该凹陷的主要烃源岩层段（沙河街组三亚段、沙河街组四亚段、孔店组）,分析结果表明:在水体浅、蒸发作用强烈的孔店组—沙四下亚段强氧化性滨浅湖环境里,钙、锶含量和Ca/Mg、Sr/Ba、Sr/Ca参数值具低值响应,铁、铝、钡、钒含量和（Fe+Al）/(Ca+Mg)参数值具高值响应;在沙四中亚段膏岩、盐岩等普遍发育的盐湖环境中,钠、锶含量和Sr/Ba、Fe/Mn、Sr/Ca均出现高值响应,锰、钡、钒含量和V/Ni、(Fe+Al)/(Ca+Mg)出现低值响应;在还原性的沙四上亚段半咸化深湖环境中,钾、钠、铁含量和Fe/Mn值具低值响应,钙、锰含量具高值响应;在沙四中亚段膏盐与泥岩共生体系中元素分布离散性明显,呈现波动性特征;Sr/Ba、Sr/Ca在盐湖环境中出现显著的高值响应,被证实可以作为良好的水体盐度指标参数,Fe/Mn、(Fe+Al)/(Ca+Mg)随水体加深逐渐增大,是良好的水体深浅指标参数。元素分布受沉积环境、岩性特征等多种地质因素的影响,在利用元素含量分布及特征元素比值来判断某单个地质因素的变化时,应该应用多种参数,进行综合判断。     

南海北部陆坡西沙海槽XS-01站位沉积物孔隙水的 地球化学特征及其对天然气水合物的指示意义*

天然气水合物是近年来国际上发现的一种新型能源,大量赋存在海底沉积物中。西沙海槽位于南海北部陆坡区,周边有多个大型深水油气田区。对该区地形地貌、地质构造和沉积条件分析以及地球物理BSR分布表明,西沙海槽是我国海洋天然气水合物资源勘查的一个有利远景区。文章主要研究了位于西沙海槽最大BSR区内的XS-01站位沉积物孔隙水的地球化学特征,发现该站位孔隙水阴阳离子浓度和微量元素组成特征变化显示出可能与天然气水合物有关的明显地球化学异常,与国际上己发现有天然气水合物地区的异常相类似。因此,认为该站位是西沙海槽区最有利的天然气水合物赋存区,值得进一步的勘查工作。     

特征元素比值在沉积物物源分析中的应用——以东营凹陷王58井区沙四上亚段研究为例

利用Ni/Co、V/Co、Mg/Mn、Mn/Sr、Ba/Mn、Fe/K、Mg/Ca、Ba/Sr、Mg/Al、Al/Na十个特征元素比值,通过分布模式、物源指数、Q型聚类等方法,对东营凹陷王58井区沙四上亚段砂体物源进行了研究。沙四上亚段沉积时期,王58井区存在南北两大物源体系,王58井及其以北地区沉积物主要来自北部物源体系,王斜583和王126井及其以南地区主要为南部物源体系,中部牛114—斜1井一带具有南北混源特点。研究表明利用特征元素比值判别沉积物物源方向,能够有效地避免水动力及成岩作用的影响,更加准确地判断沉积物的物源方向。     

珠江口海域与南黄海海域表层沉积物地球化学特征

对珠江口和南黄海近海海域10个站位的表层沉积物中67种元素进行分析,试图揭示两海域近海表层沉积物中主要元素的地球化学特征,包括分布特征及其控制因素,并通过两海域元素地球化学特征,初步探讨近海沉积环境特征。通过总结两海域表层沉积物中元素含量及分布特征,可以发现,近海海域总体上以陆源沉积为主,除Ca和Sr之外,大多数元素表现出明显的亲陆性。珠江口海域和南黄海海域沉积物元素含量的对比研究显示,前者相对富集As、Cd、Hg、Sb、Sr、Ca、Rb、C,后者相对富集Al2O3、Zr、Hf、Sc、Rb、Ga、Cs、V、Co、Cr、Cu、Mn、Ni、K2O、Na2O、B、Ba、I等。与上地壳相比,Ag、As、Bi、Hg、Li、N、Pb、Sb、Se、Cl、Br、I在两海域表层沉积物中均发生明显富集;Mo、Sn均呈现分散趋势;Sr、CaO在南黄海海域明显贫化,K2O、Na2O、Ba则在珠江口海域表现出贫化;其他元素与上地壳元素丰度相近。     

Variations in chemical element compositions in different types of Holocene calcareous root tubes in the Tengger Desert,NW China,and their palaeoenvironmental significance

Calcareous root tubes (CRTs) contain abundant information about palaeoenvironmental conditions and have been used for palaeoenvironmental studies in the desert hinterlands of arid regions. However, as subclasses of CRTs, calcareous sheaths and rhizocretions are formed by different processes, and it remains unclear whether these differences produce variations in the chemical element composition. Furthermore, it remains uncertain whether variations in chemical element concentrations amongst different subclasses of the CRTs can affect palaeoenvironmental reconstructions. In this study, we collected 54 CRT samples from the Tengger Desert of northwestern China. All samples were dated by accelerator mass spectrometry (AMS) ¹⁴C dating, and the chemical element composition and concentration differences of the two CRT subclasses were determined using X‐ray fluorescence spectrometry. The CRT samples were dated to the Holocene. The calcareous sheath and rhizocretion samples contained varying concentrations of the same chemical elements. The rhizocretions had high concentrations of mobile elements (Ca, Mg and Sr) and P, whereas the calcareous sheaths had high concentrations of stable elements, including Al, Si, Ti, Zr, Rb and Ba. These differences were due to the different formation processes of the two subclasses of CRTs. Moreover, the Sr/Ca and Mg/Ca ratios in the calcareous sheaths were higher than those in the rhizocretions from the same period, but these ratio differences had little effect on palaeo‐effective moisture reconstructions at the millennial scale during the Holocene. The reconstructions were not influenced by the various CRT subclasses. The Holocene millennial‐scale moisture changes in the Tengger Desert revealed by the Sr/Ca and Mg/Ca ratios showed that there was an arid period during the Early Holocene, a humid period during the Middle Holocene and a humid to arid period during the Late Holocene.     

泌阳凹陷核桃园组微量元素演化特征及其古气候意义

泌阳凹陷下第三系核桃园组总体上表现为一个大的湖退体系，而其中的微量元素含量及有关元素比值却呈现出细微而明显的旋回变化特征。本文依据泥岩、页岩和碳酸盐岩中Ｔｉ、Ｓｒ、Ｂａ等十六种微量元素含量及Ｓｒ/Ｂａ、Ｆｅ/Ｍｎ、Ｓｒ/Ｃｕ等七种比值的变化特征，结合古盐度及岩相资料，对核桃园组沉积时的古气候作了系统的研究，基本上分出了温暖潮湿、干湿交替、炎热干旱、温热半干旱四类较为特征的古气候类型，以期为油气勘探提供依据。     

中国近海沿岸泥的地球化学特征及其指示意义

中国海域辽阔，分为渤海、黄海、东海和南海4个海区。各海区沿中国大陆均有呈斑块状或条带状的泥质沉积分布。选取各沿岸泥的代表性样品，采用先进的XRF和ICP－MS等方法，测定了K、Li、Rb、Cs、Mg、Ca、Sr、Ba、Al、Fe、Ti、Be、Nb、Ta、W、Sn、Bi、La、Ce、Th。元素的地球化学研究表明：渤海和黄海、东海、南海沿岸泥的地球化学特征分别与黄河、长江、珠江沉积物的地球化学特征一致，显示了元素的物源效应；从渤海到南海，由于气候的变化使沿岸泥中某些元素有所流失或富集，显示了元素的气候效应；中国沿岸泥元素的丰度相对接近中国大陆沉积物的丰度，而异于西太平洋褐色粘土和深海粘土的丰度，显示了元素的亲陆性。     

Geochemical characteristics of sediment pore water from Site XS-01 in the Xisha trough of South China Sea and their significance for gas hydrate occurrence

Gas hydrate is a recently-found new source of energy that mostly exists in marine sediments. In recent years, we have conducted gas hydrate exploration in the South China Sea. The Xisha trough, one of the promising target areas for gas hydrate, is located in the northern margin of the South China Sea, adjacent to several large oil and gas fields. The Xisha trough extends 420 km long with the water depth of 1 500 m in the west part and 3 400 m in the east part and deposits thick sediments with organic matter content of 0.41%–1.02%. Previous studies on topographical features, geological P-T conditions, structural geology, sedimentary geology and geophysical bottom simulating reflectors (BSR) in the Xisha trough suggest that this area is favorable for the formation and accumulation of gas hydrate. In this paper, we present geochemical analyses for the sediment and pore water from a piston core at Site XS-01 in the Xisha trough. Seven pore water samples were analyzed for their anion (Cl⁻, SO₄ ²⁻, Br⁻, I⁻) contents, cation (Na, K, Ca, Mg) contents and trace element (Li, B, Sr, Ba, Rb, Mn) contents. Eight sediment samples were analyzed for stable carbon and oxygen isotopic compositions. A number of geochemical anomalies such as anions (e.g. Cl⁻, SO₄ ²⁻), cations (e.g. Ca, Mg) and trace elements (e.g. Sr, Ba, B) were found in this study. For example, the concentrations of Cl⁻ and SO₄ ²⁻ in pore water show a decreasing trend with depth. The estimated sulfate/methane interface (SMI) is only 18 m, which is quite similar to the SMI value of 23 m in the ODP164 Leg 997 at Blake Ridge. The Ca, Mg and Sr concentrations of pore water also decrease with depth, but concentrations of Ba, and Mg/Ca and Sr/Ca ratios increase with depth. These geochemical anomalies are quite similar to those found in gas hydrate locations in the world such as the Blake Ridge and may be related to the formation and dissociation of gas hydrates. The salt exclusion effect during the gas hydrate formation will cause an increase in major ion concentrations in the pore waters that diffused upward such as Cl. The anaerobic methane oxidation (AMO) may lead to the change of SO₄ ²⁻ and other cations such as Ca, Mg, Sr and Ba in pore water. Low δ ¹³C value of authigenic carbonates is a good indicator for gas hydrate occurrence. However, the bulk sediment samples we analyzed all show normal δ ¹³C values similar to biogenic marine carbonates, and this may also suggest that no gas hydrate-related authigenic carbonates exist or their amount is so small that they are not detectable by using this bulk analytical method. In conclusion, we suggest that the Site XS-01 in the Xisha trough of the northern margin of the South China Sea is a potential target for further gas hydrate exploration. Translated from Quaternary Sciences, 2006, 26(3): 442–448 [译自: 第四纪研究]     

Barium in Deccan Basalt Rivers: Its Abundance, Relative Mobility and Flux

The concentration of dissolved Ba in a number of rivers having their drainage almost entirely in Deccan Trap basalts has been measured. These results along with available data on the abundances of major elements in these waters, and on Ba and major elements in bed sediments of these rivers provide a measure of (i) the relative mobility of Ba during chemical weathering and erosion of basalts, particularly with respect to alkaline earths, Mg, Ca and Sr, and (ii) the flux of Ba out of the Deccan and its global significance. The concentration of dissolved Ba ranges from 8 to 105 nM. The average Ba/Mg*, Ba/Ca* and Ba/Sr (* is concentration corrected for atmospheric contribution) in waters is lower than the corresponding mean ratios in Deccan basalts, though they overlap within errors. Majority of the water samples, however, have ratios less than that in basalts. These findings can be interpreted as a cumulative effect of limited release/mobility of Ba during chemical weathering and erosion of basalts and its reactive behaviour in waters which promote its association with clays and oxy-hydroxides of Fe. These results also indicate that during chemical erosion of Deccan basalts, Ba is the least mobile among the alkaline earth elements. The abundance of Ba in sediments and their Ba/Al ratios relative to basalts are consistent with the above conclusion. Ba/Mg and Ba/Ca ratios in water and in sediments from the same location are strongly correlated; however, the mean ratios in waters are far less than those in sediments. This is a result of limited Ba mobility, effectively 5–6 times lower than that of Mg. The annual flux of dissolved Ba out of the Deccan Traps is ~1 × 10⁷ moles, ~ 0.2% of its global riverine transport to oceans. The contribution of dissolved Ba from Deccan Traps, seem lower than its aerial coverage, ~ 0.5% of the global drainage area; the potential causes for this could be the lower abundance of Ba in basalts relative to “average continental crust”, and its behaviour during chemical weathering and erosion.     

Magnesium isotope systematics of the lithologically varied Moselle river basin, France

Magnesium and strontium isotope signatures were determined during different seasons for the main rivers of the Moselle basin, northeastern France. This small basin is remarkable for its well-constrained and varied lithology on a small distance scale, and this is reflected in river water Sr isotope compositions. Upstream, where the Moselle River drains silicate rocks of the Vosges mountains, waters are characterized by relatively high ⁸⁷Sr/⁸⁶Sr ratios (0.7128-0.7174). In contrast, downstream of the city of Epinal where the Moselle River flows through carbonates and evaporites of the Lorraine plateau, ⁸⁷Sr/⁸⁶Sr ratios are lower, down to 0.70824.Magnesium in river waters draining silicates is systematically depleted in heavy isotopes (δ²⁶Mg values range from −1.2 to −0.7‰) relative to the value presently estimated for the continental crust and a local diorite (−0.5‰). In comparison, δ²⁶Mg values measured in soil samples are higher (∼0.0‰). This suggests that Mg isotope fractionation occurs during mineral leaching and/or formation of secondary clay minerals. On the Lorraine plateau, tributaries draining marls, carbonates and evaporites are characterized by low Ca/Mg (1.5-3.2) and low Ca/Sr (80-400) when compared to local carbonate rocks (Ca/Mg = 29-59; Ca/Sr = 370-2200), similar to other rivers draining carbonates. The most likely cause of the Mg and Sr excesses in these rivers is early thermodynamic saturation of groundwater with calcite relative to magnesite and strontianite as groundwater chemistry progressively evolves in the aquifer. δ²⁶Mg of the dissolved phases of tributaries draining mainly carbonates and evaporites are relatively low and constant throughout the year (from −1.4‰ to −1.6‰ and from −1.2‰ to −1.4‰, respectively), within the range defined for the underlying rocks. Downstream of Epinal, the compositions of the Moselle River samples in a δ²⁶Mg vs. ⁸⁷Sr/⁸⁶Sr diagram can be explained by mixing curves between silicate, carbonate and evaporite waters, with a significant contribution from the Vosgian silicate lithologies (>70%). Temporal co-variation between δ²⁶Mg and ⁸⁷Sr/⁸⁶Sr for the Moselle River throughout year is also observed, and is consistent with a higher contribution from the Vosges mountains in winter, in terms of runoff and dissolved element flux. Overall, this study shows that Mg isotopes measured in waters, rocks and soils, coupled with other tracers such as Sr isotopes, could be used to better constrain riverine Mg sources, particularly if analytical uncertainties in Mg isotope measurements can be improved in order to perform more precise quantifications.     

Geochemistry of Jizan shelf sediments, southern Red Sea coast of Saudi Arabia

Surface sediments from the Jizan shelf, southern Red Sea, were analysed for grain size and mineralogical and elemental composition in order to establish their geochemical characteristics. Texturally, sediments are classified into sand and mud; the latter dominates the shelf. Grain size variability and mineralogical assemblages present in the sediments largely control the abundance and distribution of CaCO₃, organic carbon content (OC) and the major and trace elements. Sand sediments are composed of carbonate material of marine origin and contain high concentrations of Ca, Mg and Sr. Mud sediments are relatively rich in OC and are characterised by high concentrations of Al, Fe, Ti, Mn, Cu, Cr, Co, Ni, V and Ba. Unlike the sand, Mg concentration in the mud sediments seems to be controlled by stronger contribution from non-carbonate material. Factor analysis is applied to identify the variables accounting for most of the variance in the mud sediment samples. Three factors are found to describe about 78% of the variance. The first factor which accounts for 41% of the total variance is the Fe and Mn oxides that reach the area through episodic flooding. The second and third factors are the mud (22%) and the mineralogy (15%) of the sediments, respectively.     

南海神狐海域Site 4B沉积物地球化学特征及其对甲烷渗漏的指示意义

前人对Site 4B站位海底浅表层沉积物的研究显示该站位历史上可能存在甲烷渗漏事件。为研究该站位的甲烷渗漏历史,分析了Site 4B站位柱状沉积物的元素地球化学特征,及沉积物中Mg/Ca和Sr/Ca比随深度的变化规律以及自生碳酸盐矿物的分布特征。元素相关性分析表明:研究区Ca、Sr等碳酸盐相关的元素极有可能来自于与甲烷渗漏有关的自生碳酸盐。结合沉积物的粒度特征,认为Site 4B站位在15.78 ka B.P.之前泥火山活动造成甲烷渗漏,且甲烷渗漏速率具有增大—减小的周期性变化特点。研究站位在24.15 ka B.P.、27.47 ka B.P.、31.05 ka B.P.具有相对较高的甲烷渗漏速率,且在31.05 ka B.P.达到最大值。研究结果对探明南海北部的甲烷渗漏历史具有重要的意义。     

Impacts of grain size sorting and chemical weathering on the geochemistry of Jingyuan loess in the northwestern Chinese Loess Plateau

Major and trace elemental compositions of loess samples collected from the Jingyuan section in the northwestern Chinese Loess Plateau (CLP) were analyzed to investigate the potential impacts of grain size sorting and chemical weathering on the loess geochemistry and to extract appropriate geochemical indices for better evaluating the East Asian monsoon variability. Based on variations of major and trace elements in different grain size fractions, seventeen elements were classified into three types: (1) Si and Na display higher contents with the increased particle sizes; (2) Al, Fe, Mg, K, Mn, Zn, Rb, Cr, V are mainly enriched in fine size fractions; (3) Ti, Ba, Zr, P, Ca and Sr show irregular variations among different size fractions. Comparison of Al-normalized elemental ratios with Zr/Rb and Rb/Sr ratios (two commonly employed indicators for grain size sorting and pedogenic weathering) indicates that Si/Al, Zr/Al, Ti/Al variations match well with Zr/Rb and grain size results, whilst Ca/Al, Sr/Al, P/Al ratios display similar variability as that of Rb/Sr ratio. Comparison of loess based proxies (e.g., elemental ratios, magnetic susceptibility, grain size) of Jingyuan section with speleothem and ice-core records confirms that elemental ratios of high-resolution loess sequences developed in the northwestern CLP can be employed to address fluctuations of the winter monsoon-induced grain size sorting and summer monsoon-related weathering and pedogenesis at glacial–interglacial and millennial timescales.     

Fractionnement des éléments en trace Li,Rb, Ba,Sr dans les séries andésitiques et shoshonitiques du Pérou. Comparaison avec d'autres zones orogéniques

In the calc-alkaline rocks of Peru, the rubidium content and the K/Ba, Rb/Sr ratios increase, while the strontium content and the K/Rb, Ba/Rb ratios decrease according to the distance of the trench. It is suggested that theses variations are related to a fractionation of plagioclase and contamination with differential migration of mobile elements. A comparative study between andesites of various localities shows in Peru an enrichment in Rb, Sr and Ba and a disparition of the Rb-Ba correlation; this last observation looks characteristic of continental margin andesites. The shoshonitic rocks differ from the andesites by a high content of Sr and Ba. The genetic relationships between these two kinds of rocks are discussed. It appears that the shoshonites are originated from a different magmatic source.     

黄土高原南部全新世黄土-古土壤 序列若干元素分布特征及意义*

选择黄土高原南部的XJN,XMC和JYC全新世剖面为研究对象。通过对地层中Ca,Ba,Rb和Sr元素分布的研究,发现Ba/Sr和Rb/Sr比值在不同地层中含量差异十分明显,并与成土作用强度显著正相关,可作为良好的气候替代指标;表生环境中Rb和Ba较稳定,Sr和Ca元素十分活跃,易于迁移,其中Ca的迁移能力高于Sr元素;从XJN→XMC→JYC剖面,Rb和Ba元素含量增加,而Sr和Ca元素含量降低,这与区域环境差异有关;全新世中期暖湿的亚热带气候主要出现关中盆地地区,六盘山以西则是暖温带气候。     

内蒙古二连浩特北部阿仁绍布地区晚石炭世花岗岩Sr-Yb分类及其成因

对分布在内蒙古二连浩特北部阿仁绍布地区的晚石炭世花岗岩类,依据Sr、Yb含量,划分为低Sr高Yb型、极低Sr高Yb型和低Sr低Yb型花岗岩3种类型。低Sr高Yb型花岗岩类相对低Si、富Al,Na2O〉K2O,稀土元素分馏中等,有或无负Eu异常,Sr含量低,平均为183×10-6,Ba含量较高,平均585×10-6,Y含量高,平均30.06×10-6,Rb/Sr比值较低,平均0.97;极低Sr高Yb型花岗岩富Si、REE,低Al、Sr、Ba,高的Rb/Sr比值（平均为7.47）,具明显的负Eu异常等;低Sr低Yb型花岗岩富Si,贫Al、Ca、Mg,重稀土元素（Y、Yb）含量低,Y含量在（7.26～10.6）×10-6之间,平均9.76×10-6,Yb含量在（1.04～1.89）×10-6之间,平均1.44×10-6,δEu=0.64～0.94,具弱负Eu异常,微量元素Ba含量高,Rb/Sr比值低。3种类型的花岗岩类过铝指数（A/CNK）多小于1.0,说明它们均源自变质火成岩的部分熔融。由于源区的深度不同（pT条件不同）和残留的主要矿物相不同,它们的岩石地球化学特征存在差异。极低Sr高Yb型花岗岩形成深度最浅（中上地壳）,熔融残留相以斜长石为主;低Sr高Yb型花岗岩类形成于中下地壳,熔融残留相为斜长石和辉石;低Sr低Yb型花岗岩形成深度最深,推测可能形成于加厚下地壳（〉40km）底部,熔融残留相为石榴子石、斜长石和角闪石。     

Statistical assessment of geochemical pattern in overbank sediments of the river Sava,Croatia

Four overbank profiles from the three terraces of different age were sampled in 10 to 20 cm intervals for the bulk content of major and minor (Ca, Mg, Fe, Ti, Al, Na, K and P) and trace (Mo, Cu, Pb, Zn, Ni, Co, Mn, As, U, Th, Sr, Cd, Sb, V, La, Cr, Ba, W, Zr, Ce, Sn, Y, Nb, Ta, Sc, Li, Rb and Hf) elements in the minus 0.125 mm fraction. Univariate statistics together with analysis of variance discriminated between the lower-lying carbonate (CA) population dominantly composed of carbonates and the overlying silicate (SI) population being dominantly of silicate mineralogy. This stratified pattern resulted from the intensive erosive action of melting glaciers exerted on limestones and dolomites in the alpine region, followed by local inputs mainly of silicate composition. Elements exhibiting the greatest between-population variability are Ca and Mg being enriched in the CA population and Fe, Mn, P, Sr, Al, Na, K, Li, Rb, Y, Zr, Ni, Cr and Ti being enriched in the SI population. Anomalously high Hg, Pb and Ba concentrations (maximum values: 6,500±2,860 ppb, 225±13 ppm and 1,519±91 ppm, respectively) in the lowermost part of the profile S7, which is nearest to the Croatian-Slovenian border, derive from the mineralized Slovenian catchment area. This profile also contains trimodal frequency distributions of Fe, Mn and P whose highest concentrations coincide with increased values of Zn and Cu which are bimodally distributed. Geochemical patterns of majority of elements in all four profiles consistently reflect the average compositions of the upstream drainage basins.