Systematic change of foraminiferal Mg/Ca ratios across a strong salinity gradient

The Mg/Ca ratio of foraminiferal calcite is an important proxy for estimating past ocean temperatures. Used in conjunction with δ¹⁸O of foraminiferal calcite it allows deconvolution of temperature and ice-volume signals to infer past ocean temperatures and salinities (assuming the relationship between seawater δ¹⁸O and salinity is known). Such work assumes that temperature is the only, or at least the dominant, environmental controller of foraminiferal Mg/Ca. The semi-enclosed Mediterranean Sea, where salinity varies from 36 to 40 psu over a seasonal temperature range of between only 5 °C to 8 °C, provides a relevant setting to test this assumption outside the laboratory. In this study, planktonic foraminifera (O. universa, G. siphonifera, G. bulloides and G. ruber (white) and (pink)) were picked from 11 box core tops spanning the Mediterranean salinity gradient and analysed for their trace-element concentrations. Mg/Ca ratios are higher, for the associated calcification temperatures, than in other regions where calibrations have been conducted and correlate poorly with calcification temperature. Mg/Ca ratios are particularly high for samples from the Eastern Mediterranean where salinity is unusually high. Correlations of Mg/Ca with the calcification salinity are statistically significant with Mg/Ca changing by 15–59% per psu, suggesting that salinity may act as a control on Mg/Ca ratios in addition to the dominant temperature control. We show that contamination by non-carbonate material and diagenetic high-Mg carbonate overgrowths cannot account for the observed trend of increasing Mg/Ca with salinity. A relationship between Mg/Ca and salinity is also suggested by re-analysis of calibrations from open-ocean settings. These new Mediterranean results are from a region with unusually high salinity but suggest that the effects of salinity on the Mg/Ca palaeothermometer should be considered even in open-ocean settings, particularly where large salinity changes occurred in the past.     

Characteristics and environmental significance of Ca, Mg, and Sr in the soil infiltrating water overlying the Furong Cave, Chongqing, China

This paper explores the influence of the local meteoric conditions,the overlying soil on the concentrations of Ca,Mg,and Sr,and the ratios of Mg/Ca,Sr/Ca,and Mg/Sr in soil infiltrating water(SIW).An in situ monitoring program was carried out above the Furong Cave throughout 2010 to collect data on SIW,monthly temperature and rainfall,and the geochemical composition and granularity of soils.The discharge of SIW responded quickly to the local rainfall,and its residence time was the primary factor affecting the Ca,Mg,and Sr content of the SIW.The high concentrations of Ca,Mg,and Sr in the SIW during April should be attributed primarily to the prolonged residence of SIW in the soil during the local dry seasons of winter and early spring.The maximum Mg/Sr ratio also occurred in April.The ratio of Mg/Ca in SIW is positively correlated with prolonged residence time and with high temperatures,which do not strongly affect the ratio of Sr/Ca.The Mg/Ca ratio was lowest when the Sr/Ca ratio was highest because plant metabolism increased the absorption of Ca and Mg,but not Sr,and also because higher temperatures enhanced the dissolution of Mg more than that of Sr.These different responses of Mg and Sr to temperature increases resulted in high Mg/Sr ratios during July and August.     

西藏扎布耶湖ZK91-2钻孔沉积特征与气候环境演化

扎布耶盐湖位于西藏高原腹地,１９９１年在其南部干盐滩中钻取了２０Ｍ深湖相沉积,以５～１０ＣＭ／个的密度进行高分辨率取样,详细探讨了沉积标志,矿物组合（尤其Ｍｇ,Ｃａ,Ｌｉ碳酸盐）、干旱与潮湿两种气候类型的元素组合等气候环境指标,推导了晚更新世以来该湖区湖面涨缩,水质咸淡及气温高低变化。     

Minor element geochemistry of groundwater from an area with prevailing saline groundwater in Chikhwawa,lower Shire valley (Malawi)

Groundwater resources with high salinity content are found in some parts of the lower Shire River valley (Malawi). This paper discusses the geochemistry of minor elements with regards to the prevailing salinity. Hierarchical clustering and principal component analyses were used to identify factors which relate to both minor elements and samples and were interpreted as reflecting the influence of prevailing saline/brackish groundwater. Concentrations of lead (Pb), boron (B), strontium (Sr) and chromium (Cr) were associated with groundwater with high content of total dissolved solids (TDS). Speciation calculations indicated that dissolved Sr, barium (Ba) and lithium (Li) were mainly in the form of free aqueous ions whereas hydrolysed species were significant for aluminium (Al) and Cr, and carbonate complexes for Pb. Chloride complexes were prevalent for silver (Ag). Solubility of cerussite (PbCO₃) and barite (BaSO₄) was shown to act as a control on the levels of Pb and Ba, respectively. Thus, Ba concentrations were very low in saline groundwater owing to their high sulphate content. A relatively variable B concentration in the groundwater samples was explained using a binary mixing model of saline and fresh groundwater. The mixing of fresh groundwater with saline groundwater was concomitant with high Na⁺/Ca²⁺ ratios and enrichment of B, probably by desorption from clays. The WHO drinking water guidelines for Ba, B, Cr and Pb were exceeded in 6.5%, 9.7%, 16.1% and 64.5% of all the samples, respectively. However, all samples were below the Malawian specification of B in borehole and shallow well water quality (MS 733:2005) of 5.0 mg/L.     

Composition of island arcs and continental growth

Island arc volcanism has contributed and is still contributing to continental growth, but the composition of island arcs differs from that of the upper continental crust in its lower abundance of Si, K, Rb, Ba, Sr and light rare earth elements. In their advanced stage of evolution, island arcs contain more than 80% of tholeiitic and 15% of ‘island arc’ calc-alkaline rocks with varied SiO₂ contents. The larger proportion of tholeiitic rocks is in the lower crustal levels. The high stratigraphical levels of the island arcs are composed of tholeiitic plus calc-alkaline and/or high potash (shoshonitic) associations with higher abundances of K, Rb, Sr, and Ba. Stratification of the island arc crust is accentuated by another type of calc-alkaline volcanism (Andean type) originating at a late stage of arc evolution, probably by partial melting at the base of the crust. This causes enrichment of the upper crust in K, Rb, Ba and REE and accounts for upper crustal abundances of these elements as well as of SiO₂.     

利用介形类壳体Sr, Mg重建古环境受自生碳酸盐矿物的限制及机理探讨

以云南鹤庆盆地HQ孔上部15~55 m沉积物中2个不同种属的介形类壳体为研究对象, 通过比较壳体中Sr/Ca, Mg/Ca之间及其与沉积物Sr含量的关系, 得出以下结论: (1) 壳体Sr/Ca, Mg/Ca首先反映的是该介形类生存的微生态环境; (2) 壳体Sr/Ca较Mg/Ca更好地线性响应水环境的变化, 但当体系中有文石结晶沉降时Sr/Ca不再线性响应湖泊水体盐度的变化; (3) 壳体的Sr/Ca完全受控于湖水盐度及水体中自生碳酸盐矿物的结晶过程, 而壳体中的Mg/Ca则受湖水盐度和温度控制, 实际上温度只是壳体生长速率对壳体Mg/Ca控制的外在表现. 建议在以后的古环境重建及室内培养实验时, 更多地关注沉积物组成及其自生矿物结晶对生物壳体微量元素(如Mg/Ca, Sr/Ca)组成的制约.     

青藏高原湖泊Mg~(2+)、Ca~(2+)和Mg/Ca盐度指示意义的初步分析

总结了青藏高原地区400多个湖泊湖水的Mg2+、Ca2+和Mg/Ca等水化指标与湖水盐度的相关关系,以及这种关系随着湖水变化(不同采样时间和采样点以及自然蒸发)而产生的变化规律.结果表明:青藏高原湖泊湖水的Mg2+浓度与盐度具有较为稳定的正相关关系,而Ca2+和Mg/Ca与盐度的相关性较弱.在对于某一特定水化学类型的湖泊,一般碳酸盐型湖泊的Mg2+、Ca2+以及Mg/Ca等指标与盐度均没有明显的相关性;硫酸盐型湖泊中Mg2+浓度和盐度呈现较高的正相关关系,而Ca2+以及Mg/Ca与盐度的相关性仍很弱;而在氯化物型湖泊中,Mg2+浓度与盐度呈更高的正相关性,Ca2+浓度也与盐度呈一定的正相关性,Mg/Ca这一指标与盐度的相关性依然很弱.而对某一特定湖泊,在不同演化阶段或不同的采样地点,Mg2+浓度与盐度仍然保持明显的正相关关系,而Ca2+以及Mg/Ca与盐度的相关性仍然不稳定或很弱.在青藏高原作古环境重建应用的时候,湖水Mg2+浓度是古盐度一个较好的转换指标,而Ca2+以及Mg/Ca的古盐度指示意义相对较弱.     

近1800年以来内蒙古达里湖浮游植物群落演变及驱动因素

湖泊是地质历史上区域生态环境演变的重要载体,其沉积物中包含了丰富的环境演变信息。达里湖是典型的草原内陆封闭型湖泊,位于东亚夏季风的北部边缘,地理位置关键。本研究基于在达里湖采集的约238 cm沉积物岩芯 (GDL-1),通过²¹⁰Pb和¹³⁷Cs (岩芯上部20 cm)、AMS¹⁴C测年,以及沉积物样品中甾醇等生物标志物含量分析,重建了近1800年以来达里湖硅藻、蓝藻等典型藻类含量的演化历史,并结合总氮(TN)、总磷(TP)、盐度(Sr/Ba)和温度(T)等环境代用指标,分析藻类群落的主要影响因素。结果显示达里湖典型藻类总量平均为2.03 ng/g(最高6.69 ng/g,最小0.53 ng/g),其中蓝藻占比平均为60%,绿藻和硅藻占比平均为20%;环境因子对硅藻、蓝藻和典型藻类生物量的解释率分别为47.7%、55.20%和48.10%,T、TN和Sr/Ba是影响浮游植物群落的主要影响因素;硅藻占比与温度呈显著负相关,小冰期硅藻占比最高,中世纪暖期占比最低;在达里湖的高盐环境下,湖泊营养盐浓度对藻类的影响受到限制,成为藻类等生长的限制因素;Sr/Ba小于0.9时,硅藻含量与典型藻类总量随着Sr/Ba值的升高而增加,Sr/Ba大于0.9时,典型藻类总量与Sr/Ba值呈负相关关系,而硅藻则表现出对盐度具有一定的耐受性;整体上,近1800年以来,区域或全球性气候事件通过改变达里湖盐度、营养元素浓度和温度来影响典型藻类群落结构。在暖期阶段,蒸发作用增强等导致的湖泊盐度增加成为达里湖典型藻类群落结构演变的主要影响因素;在冷期,营养元素浓度和温度的降低成为湖泊水体浮游植物生物量的主要影响因素。     

青藏高原东部兴措湖生物壳体元素及同位素记录的气候环境信息

通过对青藏高原东部若尔盖盆地兴措湖50年来Gyraulus sibirica壳体元素及同位素分析,并与器测气象资料的比较,建立了兴措湖记录与对应的降水和气温间的函数关系,探讨了湖泊记录所指示的气候环境意义,结果表明：青藏高原东部兴措湖地区腹足类生物在夏半年形成壳体,它所记录的是夏半年而不是全年的气候环境信息,Gyraulus Sibria壳体Mg/Ca比及δ^18O指标与夏半年气温有一定的相关性,其中壳体δ^18O指标对气温变化更敏感,δ^18O与夏半年气温滑动平均间的变率为1．64‰／℃,均值比为0．28‰/℃,Sr/Ca比,δ^13C指标与夏半年的降水量关系较密切,尤其是Sr/Ca比随降水量波动呈显著相关变化,Sr/Ca变化与降水间的平均变率（d(Sr/Ca)/dP)为－0．045/mm。     

东营凹陷波动古湖相烃源岩沉积特征

以东营凹陷牛38井为例,研究显示,该井沙河街组沙三段烃源岩的沉积特征具有明显的波动性．宏观上体现为, 构造因素控制湖盆的整体升降和沉积构造旋回,但季节性气候及其它因素的影响使湖盆呈现次级旋回的复合性沉积．微观上表现为纹层的不连续性及生物扰动构造等事件性沉积.古湖面不同幅度的波动和变化导致相对稳定的泥岩沉积的不稳定性,有机质的分布也呈现较显著的非均质性．湖泊的沉积过程影响了微量元素、有机质以及烃源物质的分布,水体较深、盐度较高的沙三段下部多数微量元素含量较高以及B／Ca、Sr／Ba呈现高值;水体较浅、盐度较低的沙三段中部各元素的分布较为稳定,B／Ca、Sr／Ba比值及Sr的含量均显著降低.波动性沉积导致烃源岩呈现明显的优劣性分布,沙三段下部中的有机质富集,为优质烃源岩;沙三段中部的有机质分布较为分散,生排烃的资源潜力有限．     

重庆芙蓉洞土壤带Mg和Sr元素特征及其环境意义

通过在2010年对重庆武隆芙蓉洞上覆土壤带的定点监测,收集土壤渗透水,结合当地气温、降水量、土壤地球化学组成和土壤粒度组成,探讨气候条件和土壤层对渗透水中Ca,Mg和sr元素浓度以及Mg／Ca,St／Ca和M∥sr比值的影响．数据显示土壤渗透水量可以快速反映地表降水量的变化,冬季和春季时（旱季）土壤渗透水在土壤中滞留时间延长是导致Ca,Mg和Sr浓度在4月出现高值的主要因素．土壤渗透水中Mg／Ca比值随着土壤渗透水滞留时间的延长和温度升高而升高,而Sr／Ca比值与降水量和气温的关系不明显．植物生长活动对ca和Mg元素的吸收强度大于对Sr元素的吸收,并且Mg的溶蚀能力相对于Sr更易于响应温度的升高,由此导致Mg／Ca与Sr／Ca比值之间呈现反相关关系．冬春旱季时土壤渗透水在土壤中滞留时间的延长导致了Mg／Sr比值在4月出现高值;而Mg/Ssr比值在7月和8月出现高值则是因为在温度升高的情形下渗透水对Mg的溶蚀相对于Sr更强．     

湖相介形类壳体地球化学在环境变化研究中的应用与进展

双壳微体甲壳类动物介形虫,广泛分布于各类湖泊体系中,其碳酸盐壳化石通常在湖泊沉积物中保存完好,介形类的古生态学,尤其是介壳的地球化学在环境变化研究中,近年来得到越来越广泛的应用,介壳的氧同位素组成四形成壳体时湖水的同位素组成和温度决定,可以反映由蒸发和降水的变化所引起的湖水水化学以及与之关联的气候变化情况,一般而言,低δ^18O反映了温度潮湿的气候;高δ^18反映了寒冷干燥的气候,碳同位素可以反映总溶解无机碳的组成以及影响其组成的诸因素的变化,多数情况下可以反映湖泊古生产力的大小及变化,介壳中Mg和Sr的含量,往往与其宿生水体的盐度和温度呈一定的函数关系,据此可以恢复湖泊的温度,尤其是盐度的变化,为了满足高分辨率环境变化,特别是定量研究的要求,必须充分了解介形类各个种属的生命历史和生态消长的过程;通过定期收集野外介壳和水样进行化学分析了,了解湖水水化学和温度对介壳稳定同位素和微量元素组成的影响;详细了解湖泊湖沼学,包括湖水的同位素组成和M/Ca（M指微量元素Mg、Sr等）与盐度的关系以及它们随空间和季度变化的特征;开展实验室养殖培养实验,测定单个种属介壳与水体的氧同位素分馏系数,建立微量元素吸收的生理效应。     

泥炭沼泽不同植物群落中地表糙度变化及其影响机制

对藏南沉错CCl孔216个沉积物样品进行了15种金属元素含量的测试,研究金属元素含量的分布特征,以及与粒度参数的变化关系．结果显示：金属元素的分布特征可分为三组,K、Na、Mg、Al、Ti、Ba、Cu、Zn、Fe、Pb、Cr、V等12种元素具有较为相似的变化趋势;Ca和Sr变化趋势相同;而Mn与其他任何一种元素都不相似．元素分布与粒度参数的相关分析结果表明,Ca、Ti、Pb的变化与沉积物粒度没有明显的关系;K、Na、Al、Ba、Cu、Fe、Cr、V等8种元素与沉积物粘土含量（〈4um）呈正相关关系;Mg、Zn、Mn与粉砂含量（4—63μm）呈正相关关系;而Sr与砂含量（〉63gm）呈正相关关系本研究中大部分元素的粒度效应与其他湖泊、海洋等水体沉积物中元素的粒度效应具有一致的结果．与本岩芯已有的过去1400年来的环境重建资料对比可以发现,在不同的环境变化阶段,元素组合特征都与湖区环境状况具有较好的对应性．其中大部分元素的含量变化受物源条件即流域风化侵蚀程度的影响,而Ca含量不受沉积物粒度变化影响,且与沉积物中碳酸盐含量、Sr／Ba具有很好的相关性,说明其变化受物源条件影响小,而主要与湖水理化性质、蒸发强度以及湖泊沉积过程有关．     

生物壳体锶地球化学恢复盆地古水文——以泥河湾盆地为例

本文以著名的泥河湾盆地小渡口剖面28层为实例,通过有孔虫,介形虫,腹足类微体生物壳体87Sr/86Sr比值与盆地汇水区域Sr同位素地层分布特征对比分析以及生物壳体Sr/Ca国度的相关性,来重塑沉积盆地汇水来源变更,湖水变化等古水文要素,进而可以反演区域构造－气候变化,实例研究结果表明,生物壳体87Cr/86Sr 及Sr/Ca比值等地球化学方法是恢复盆地古水文条件的重要手段。     

利用泥质岩硼含量重建过去湖泊古盐度和湖面变化历史

根据封闭湖泊古盐度与湖面变化之间具有反向变化的特点,以沱沱河地区通天河剖面为例,利用泥质岩的硼元素含量作为古盐度计,重建了青藏高原北部地区晚渐新世-早中新世湖泊沉积的古盐度变化曲线,讨论了应用湖水古盐度变化曲线追踪过去湖平面变化历史的适用范围和局限.结果表明:雅西错组上部古湖泊水体的盐度一般处于咸水湖分布区,盐度变化于微咸水到超咸水范围内,指示渐新世晚期气候干燥,湖平面长期处于低水位期;但中新世早期五道梁组沉积期,高原气候开始向湿润方向发展,湖水古盐度明显下降,湖水位快速上升.     

Constraints of authigenic carbonates on trace elements (Sr, Mg) of lacustrine ostracod shells in paleoenvironment reconstruction and its mechanism

Molar ratios of Mg/Ca and Sr/Ca were measured in two species of ostracod shells preserved in the upper core (15-55 m) of the Heqing Basin in Yunnan Province, southwest China. By correlating the molar ratios between Mg/Ca and Sr/Ca and comparing them with Sr concentrations of the sediments, we suggested that: (1) the molar Mg/Ca and Sr/Ca ratio variations in respective ostracod primo re- flected the changes in its ambient water composition and ecology; (2) the molar Sr/Ca ratios responded better to the salinity change linearly than Mg/Ca without aragonite precipitation in the system, and otherwise there was no linear relation between them; and (3) the molar Sr/Ca ratios were mainly con- trolled by salinity and authigenic carbonate precipitation, whereas the molar Mg/Ca ratios were related to both salinity and temperature. In fact, the rate of ostracod growth owing to temperature controls the fluctuation of Mg/Ca in shells. Here, more attentions should be paid to the constraint of authigenic mineral precipitation processes on the trace elements in ostracod shells and to the correlation between these trace elements in biogenic carbonates and compositions of the sediments in systems and in fu- ture in vitro experiments.     

Early precambrian trondhjemitic suites in Western Australia and Northwestern Scotland,and the geochemical evolution of shields

Sodium-rich trondhjemites and quartz keratophyres, retained as pebbles in Archaean metaconglomerates, represent some of the oldest components (up to 3 by) of the Kalgoorlie System, Western Australia. New determinations indicate high Si, Na, Na/K, Ba/Rb, Ba/K, Sr/Ca+K, Ni, Ni/Mg, and Cr/Mg, and low K, Rb, Rb/Sr, and Y, in comparison to Taylor's (1965) [1] and other' average granites and to Nockolds and Allen's (1953) [2] acid calc-alkaline rocks. Syngeosynclinal quartz keratophyres (2.6 by) studied by O'Beirne (1968) [3] show similar comparisons. Similarly, high-grade acid and intermediate gneisses of the Lewisian, Scotland, have high Na/K, K/Rb, Ba/Rb, Ba/K, Sr/Ca+K, Ni, Ni/Mg, Cr, Cr/Mg, and low K, Rb, Rb/Sr, Y and Y/Ca. Secular decrease in Na/K, K/Rb and Sr/Rb is shown by granite series in Western Australia, Transvaal, Rhodesia and the Canadian Shield. The earliest members of these series compare with sodic acid plutons of island arcs, in particular Fiji, an archipelago showing a pattern of evolution analogous to that of the proposed model (Glikson, 1971) [4]. Evidence for an origin of Archaean sodic granites from below a basic crust is furnished by the abundance of basic xenoliths, by relationships in agmatite-gneiss terrains in Greenland, Scotland, and India, by K levels lower than those of Archaean metasediments, and by low initial⁸⁷Sr/⁸⁶Sr ratios. The abundance of euhedral quartz phenocrysts in the quartz keratophyres supports origin through partial melting of eclogite [5]. In high-grade belts, the originally low abundances of K and Rb were accentuated by synmetamorphic depletion, with which the formation of late-stage K-granites may have been associated. The correlation of chemical data enables an insight into spatial and temporal relationships between low- and high-grade early Precambrian terrains, and on the geochemical evolution of shields.     

Correlation between δ~(18)O,Sr/Ca and Mg/Ca of coral Acropora and seawater temperature from coral culture experiments

To be used as proxies of seawater surface temperature(SST), the δ 18Oc values and Sr/Ca and Mg/Ca ratios of scleractinian coral skeletons must be verified by coral culture experiments in the laboratory. This paper describes a coral culture experiment that was conducted at several seawater temperatures T(21–28°C) using a tandem aquarium system and the new method for depositing coral skeletons grown under controlled conditions. The δ 18Oc values and the Sr/Ca and Mg/Ca ratios of the cultured coral were measured. We concluded that the δ 18Oc values and Sr/Ca and Mg/Ca ratios of the cultured coral are clearly correlated with T. The linear regression curve is δ18Oc(‰)=δ0.1427δT(°C)δ0.1495(n=18, r=0.955, p0.0001), and the slope of δ0.1427‰/°C is at the low end of the range of published values(δ0.13–δ0.29‰/°C). The Sr/Ca ratio decreases with increasing T, whereas the Mg/Ca ratio increases with increasing T, indicating a negative correlation between Sr/Ca and Mg/Ca. Their linear regression curves are Sr/Ca(mmol/mol)=δ0.04156δT+10.59(n=15, r=0.789, p0.005) and Mg/Ca(mmol/mol)= 0.04974δT+2.339(n=17, r=0.457, p0.05), respectively, which demonstrate that when Mg/Ca and Sr/Ca are increased by one unit, T increases by 5.19°C and decreases by 15.62°C, respectively. These variations are significantly lower than published values.     

Controls on shell Mg/Ca and Sr/Ca in cultured planktonic foraminiferan, Globigerinoides ruber (white)

Mg/Ca and Sr/Ca ratios were determined on a single species of planktonic foraminiferan, Globigerinoides ruber (white), collected from the Gulf of Eilat and cultured in seawater at five different salinities (32 to 44), five temperatures (18 to 30 °C) and four pH values (7.9 to 8.4). The Mg/Ca-temperature calibration of cultured G. ruber (with an exponential slope of 8 ± 3%/°C) agrees well with previously published calibrations from core-tops and sediment traps. However, the dependence of Mg/Ca on salinity (with an exponential slope of 5 ± 3%/psu) is also significant and should be included in the calibration equation. With this purpose, we calculated a calibration equation for G. ruber dependent on both temperature and salinity within the 95% confidence limits:

Mg/Ca(mmol/mol)=exp[0.06(±0.02)*S(psu)+0.08(±0.02)*T(°C)−2.8(±1.0)],R²=0.95