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1.
湖积物中不同无机碳酸盐矿物常常混杂在一起,其氧同位素组成(δ18O)差异会影响碳酸盐δ18O环境信息提取的可靠性。不同矿物之间δ18O差值明显且幅度不一。20~25℃时生成的白云石比共生的方解石富集18O可能为0‰~9‰不等,亦或方解石比白云石可能更富集18O达0‰~12.3‰。常温状态,相同条件下形成的文石δ18O值较方解石高出0‰~1‰,或者方解石较文石δ18O值高出0‰~4.47‰。镁方解石中MgCO3的mol百分含量每增加1%,其δ18O值相对于纯方解石δ18O值增加0.06‰~0.17‰。在利用碳酸盐δ18O进行气候及环境研究时,不能根据某种差值进行校正,而应进行单矿物测试。由此,对不同无机碳酸盐矿物的分离及同位素测试、推算方法进行了归纳和述评。 相似文献
2.
对前人提出的湖泊自生碳酸盐氧同位素组成（δ18Oc）多种环境解释模型作了评述,指出了各种模型存在的局限性。提出在利用δ18Oc变化进行气候和环境变化研究时,需注意气温对湖泊δ18Oc的影响机制,湖水不同深度层的水温差异对化学沉积和介壳碳酸盐δ18Oc的影响δ18Oc和湖泊水位、降水δ18Oc、湖水盐度的关系,碎屑和自生碳酸盐矿物的分离,湖泊不同碳酸盐矿物间δ18Oc差值的确定,单矿物同位素组成的测试,不同前处理方法对δ18Oc测定的影响,以及碳酸盐沉积时的不平衡效应等问题。 相似文献
3.
湖泊生物碳酸盐形成于湖水底层,化学碳酸盐形成于湖水表层;处于湖积物同一层位的两种成因类型的碳酸盐氧同位素组成(δ18O)差异可能反映了二者形成时的环境差异,如湖泊不同深度的水温差异、碳酸盐质生物如介形类小生境水体δ18O值、两种成因碳酸盐形成的时间先后、湖泊表层水体蒸发情况等。在进行碳酸盐δ18O环境意义分析时,应分开测试生物碳酸盐和化学碳酸盐δ18O。 相似文献
4.
湖泊自生碳酸盐δ18O(δ18Oc)是研究湖泊水体同位素平衡和气候变化的重要环境同位素指标。由于δ18Oc与湖水δ18O(δ18Ow)密切相关,前人建立了δ18Ow的计算公式,这方面的研究对于δ18Oc环境意义的正确判读十分重要。δ18Ow计算公式中的平衡分馏系数α和平衡富集系数ε各有几种计算形式,当两个参数同时出现时,其计算形式须正确组合:当α>1时,ε=α-1或ε=1-1/α;当α<1时,ε=1-α或ε=1/α-1。其中"α>1,ε=α-1"组合最常用。 相似文献
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6.
介形虫化石壳体被认为是反映古湖泊沉积环境的理想对象。在过去的30年,介形虫壳体的δ13C和δ18O测定已经被广泛应用到湖泊沉积古气候及古环境的重建。由于湖泊生物碳酸盐样品不同的前处理方法可能会影响到稳定同位素测试结果的重现性和辨析率以及实验室之间数据的可比性,采用有效的方法对介形虫壳体进行预处理是保证介壳稳定同位素测试的一个关键环节。在总结目前常用的湖泊生物碳酸盐稳定同位素测试样品处理方法的基础上,通过对青海湖现代和古代沉积物中介形虫的测定,讨论各种处理方法对介形虫壳体稳定同位素测试结果(δ13C和δ18O)的影响。实验表明:不同处理方法对所测介壳样品的δ13C值和δ18O值不会产生大的影响,在介壳样品的稳定同位素测试之前不需要对介壳样品进行处理。 相似文献
7.
青海湖Q14B沉积物柱芯560~415 cm(约14.0~10.5 ka B.P.)段,介壳1δ8O高于无机碳酸盐1δ8O可能反映了此时青海湖表层水温高于底层水温;介壳1δ8O与无机碳酸盐1δ8O之间的较小差值可能揭示了此时青海湖水位很浅,气候干冷;介壳1δ8O变幅大于无机碳酸盐1δ8O变幅,则可能源于此时青海湖水位大幅度波动导致的底层水温变幅超过表层,以及无机碳酸盐1δ8O测自全碳酸盐所致。在利用湖泊碳酸盐1δ8O进行气候及环境变化研究时,有必要分别测试不同种属介形虫及不同无机碳酸盐矿物的同位素值。 相似文献
8.
《干旱区地理》2021,44(4):934-942
选取艾比湖流域降水、地表水和地下水为研究对象,结合流域水文地质资料,利用野外调查、室内试验和统计分析等方法分析了流域不同水体氢氧稳定同位素的时空变化特征。结果表明:(1)艾比湖流域降水δ~2H和δ~(18)O变化范围分别为-148.2‰～-34.5‰和-20.16‰～1.20‰,流域大气降水线斜率为6.69。降水δ~(18)O值与气温呈正相关关系,与降水量在夏季表现出显著的负相关关系。(2)地表水δ~2H和δ~(18)O变化范围为-101.0‰～-17.0‰和-14.54‰～0.29‰,其中8月最大,其次为5月和10月。博尔塔拉河同位素值从上游到下游沿流程逐渐增加,而精河沿流程变化趋势不明显,河水δ~(18)O与气温存在正相关关系。(3)地下水δ~2H和δ~(18)O值的范围分别为-85.0‰～-65.5‰和-12.18‰～-9.05‰,平均值分别为-75.5‰和-11.00‰。博尔塔拉河区地下水同位素值从上游到下游沿流程逐渐增加,精河区沿流程变化趋势不明显。艾比湖流域水体稳定同位素的测定,为阐明流域水文过程提供同位素证据,对变化环境下有效利用水资源,维护流域生态安全具有重要意义。 相似文献
9.
巴丹吉林沙漠东南部湖泊和地下水的氢氧同位素特征 总被引：5，自引：2，他引：3
通过对巴丹吉林沙漠湖泊和地下水氢氧同位素分析,讨论了沙漠湖水和地下水的补给关系,并结合地下水可溶性固体总量的特征,进一步探讨了巴丹吉林沙漠的蒸发特性。根据氢氧同位素的分析结果,本研究区的蒸发趋势线方程为:δD=4.1δ18O-30.02‰（n=37,R2=0.94）较低的斜率显示了巴丹吉林沙漠强烈的蒸发环境特征。巴丹吉林沙漠东南部湖泊和地下水具有相似的蒸发趋势,推测两者之间存在补给关系。根据沙漠腹地地下水氧同位素值富集程度高于东南部地下水氧同位素值的特点,得出前者蒸发较后者强烈。进而对比其他干旱条件下盐湖的蒸发,结果显示巴丹吉林沙漠湖水存在过度蒸发效应。 相似文献
10.
以雅鲁藏布大峡谷的羚牛为主要研究对象,讨论其牙齿珐琅质羟基磷灰石结构碳酸盐的碳、氧同位素组成与生活环境之间的关系。羚牛牙齿的碳同位素组成分布范围相当宽,且随着栖息地海拔高度的增加而变重,反映了食谱中C4植物从无到有、由少到多的变化趋势。C4植物含量最高可能达到70％。这一变化与当地自然带的划分相吻合。羚牛牙齿珐琅质结构碳酸盐的δ18O值分布范围较窄,与海拔高度之间没有明显的相关性。氧同位素分馏可能与水源和物种均有关。 相似文献
11.
Oxygen isotopic composition and its application to the study of tracing oceanographical process in Bering Sea and Chukchi Sea 
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下载免费PDF全文 In this paper, the 18 O distribution of surface water from the central sea areas of the Bering Sea and the Chukchi Sea was studied. The δ 18 O value of surface water from the Bering Sea is averagely -0.5‰; the δ 18 O contents of the Chukchi Sea are distributionally lower in northeast and higher in southwest; the δ 18 O value at the margin of Canadian Basin is -2.8‰, and averagely -0.8‰ in the southern area of the Chukchi Sea. The δ 18 O vertical distribution in some deep water stations from the Chukchi Sea and the Bering Sea is also studied. In the southern margin of Canadian Basin, the δ 18 O value is -2‰ -3‰ for surface layer and rises to 0 at 100 m depth layer. In the Bering Sea, the δ 18 O is about -0.5‰ for surface layer and increases to 0 at the depth of 300 m. The NO tracer can reflect obviously three water masses vertically distributed in the central Bering Sea: the upper Bering water mass, the middle Bering water mass and the deep Pacific water mass. The distributive ranges of NO and temperature for the various water masses are T<7℃, NO>780 μmol/dm 3 and T≥7℃, NO>650 μmol/dm 3 for upper Bering water mass, T<4℃, 550相似文献
12.
黄土高原黄土稳定同位素与古季风研究进展 总被引：1，自引：0，他引：1
黄土高原黄土-古土壤完好地记录了过去环境信息,进入90年代以来,在利用碳、氧同位素作为气候替代指标研究古植被、降雨量、古环境温度及古季风演化方面取得了长足的进展,文章就这方面的主要研究成果作了综合分析与评述。 相似文献
13.
The Paleoproterozoic (Statherian) Thelon Basin is located in the Churchill Province of the Canadian Shield, formed following the Trans‐Hudson Orogeny. Basin formation followed an interval of felsic volcanism and weathering of underlying bedrock. The diagenetic evolution of the Thelon lasted about one billion years and was punctuated by fluid movement influenced by tectonic events. Early quartz cements formed in well‐sorted, quartz‐rich facies during diagenetic stage 1; fluids in which these overgrowths formed had δ18O values near 0‰ (Vienna Standard Mean Ocean Water). Uranium‐rich apatite cement (P1) also formed during diagenetic stage 1 indicating that oxygenated, uranium‐bearing pore water was present in the basin early in its diagenetic history. Syntaxial quartz cement (Q1) formed in water with δ18O from ?4 to ?0.8‰ in diagenetic stage 2. Diagenetic stage 3 occurred when the Thelon Formation was at ca. 5 km depth, and was marked by extensive illitization, alteration of detrital grains, and uranium mineralization. Basin‐wide, illite crystallized at ～200 °C by fluids with δ18O values of 5–9‰ and δD values of ?60 to ?31‰, consistent with evolved basinal brines. Tectonism caused by the accretion of Nena at ca. 1600 Ma may have provided the mechanism for brine movement during deep burial. Diagenetic stage 4 is associated with fracturing and emplacement of mafic dikes at ca. 1300 Ma, quartz cement (Q3) in fractures and vugs, further illitization, and recrystallization of uraninite (U2). Q3 cements have fluid inclusions that suggest variable salinities, δ18O values of 1.5–9‰, and δD values of ?97 to ?83‰ for stage 4 brines. K‐feldspar and Mg‐chlorite formed during diagenetic stage 5 at ca. 1000 Ma in upper stratigraphic sequences, and in the west. These phases precipitated from low‐temperature, isotopically distinct fluids. Their distribution indicates that the basin hydrostratigraphy remained partitioned for >600 Ma. 相似文献
14.
Chris Harris Nonkululeko Buthelezi Beth Kahle Richard Kahle Kathlego Ramahala George Smith 《Basin Research》2019,31(1):114-135
The Karoo Basin covers much of South Africa and is an area of prospective shale gas exploration, with the Whitehill Formation the target shale unit. However, the sedimentary succession, including the Whitehill, has been intruded by a series of sills and dykes associated with the Karoo Large Igneous Province (~183 Ma), which are expected to have modified the thermal history of the basin dramatically. Here, we investigate a secondary effect of these intrusions: a series of hydrothermal vent complexes, or breccia pipes, focusing on using O, H, and C isotopes to constrain the origin and evolution of fluids produced during the intrusion of basaltic sills. A cluster of breccia pipes have been eroded down to the level of the Ecca Group at Luiperdskop on the western edge of the Karoo basin; a small isolated pipe of similar appearance crops out 13 km to the east. The Luiperdskop pipes are underlain by a Karoo dolerite sill that is assumed to provide the heat driving fluidization. The pipes consist of fine‐grained matrix and about 8% clasts, on average, of mostly sedimentary material; occasional large rafts of quartzite and dolerite are also present. The presence of clasts apparently from the Dwyka Group is consistent with the depth of formation of the pipes being at, or near, the base of the Karoo Supergroup, between 400 and 850 m below present surface. The presence of chlorite as the dominant hydrous mineral is consistent with an emplacement temperature between 300 and 350°C. The major and trace element, and O‐ and H‐isotope composition of the Tankwa breccias is homogenous, consistent with them being derived from the same source. The δ18O values (vsVSMOW) of the breccias are relatively uniform (7.1‰–8.7‰), and are similar to that of the country rock shale, and both are lower than expected for shale. The water content of the breccia is between 2.7 and 3.1 wt.% and the δD values range from ?109‰ to ?144‰. Calcite in vesicles has δ13C and δ18O (VSMOW) values of ?4.2‰ and 24.0‰, respectively. The low δD value of the breccia rocks does not appear to be due to the presence of methane in the fluid. Instead, it is proposed that low δD and δ18O values are the result of the fluid being derived from the breakdown of clay minerals that formed and were deposited at a time of cold climate at ~290 Ma. 相似文献
15.
Liina Laumets Volli Kalm Anneli Poska Sándor Kele Katrin Lasberg Leeli Amon 《Journal of Paleolimnology》2014,51(1):99-111
We investigated a 3.75-m-long lacustrine sediment record from Lake Äntu Sinijärv, northern Estonia, which has a modeled basal age >12,800 cal yr BP. Our multi-proxy approach focused on the stable oxygen isotope composition (δ18O) of freshwater tufa. Our new palaeoclimate information for the Eastern Baltic region, based on high-resolution δ18O data (219 samples), is supported by pollen and plant macrofossil data. Radiocarbon dates were used to develop a core chronology and estimate sedimentation rates. Freshwater tufa precipitation started ca. 10,700 cal yr BP, ca. 2,000 years later than suggested by previous studies on the same lake. Younger Dryas cooling is documented clearly in Lake Äntu Sinijärv sediments by abrupt appearance of diagnostic pollen (Betula nana, Dryas octopetala), highest mineral matter content in sediments (up to 90 %) and low values of δ18O (less than ?12 ‰). Globally recognized 9.3- and 8.2-ka cold events are weakly defined by negative shifts in δ18O values, to ?11.3 and ?11.7 ‰, respectively, and low concentrations of herb pollen and charcoal particles. The Holocene thermal maximum (HTM) is palaeobotanically well documented by the first appearance and establishment of nemoral thermophilous taxa and presence of water lilies requiring warm conditions. Isotope values show an increasing trend during the HTM, from ?11.5 to ?10.5 ‰. Relatively stable environmental conditions, represented by only a small-scale increase in δ18O (up to 1 ‰) and high pollen concentrations between 5,000 and 3,000 cal yr BP, were followed by a decrease in δ18O, reaching the most negative value (?12.7 ‰) recorded in the freshwater tufa ca. 900 cal yr BP. 相似文献
16.
We quantified differences in oxygen isotope fractionation among three biostratigraphically important subfossil ostracod species
(Metacypris cordata, Pseudocandona rostrata and Candonopsis kingsleii) from an early Holocene freshwater tufa layer in northern Estonia. Estimated mean δ18O values are −10.05‰ for M. cordata, −9.34‰ for C. kingsleii and −8.75‰ for P. rostrata. All three species exhibit positive offset from the weighted mean annual δ18O of contemporary precipitation (−10.7‰ in δ18OV-PDB) and from the mean δ18O value of authigenic tufa carbonate (−10.64‰) in the ostracod-bearing layer. Assuming that the known oxygen isotope fractionation
in P. rostrata (+2.5‰) and M. cordata (+1.5‰) has remained constant over time, the theoretical δ18OV-SMOW of the early Holocene lake water was calculated to have been between −11.52 and −11.92‰, slightly less negative than the
local Ordovician groundwater (−11.7 to −12.2‰). δ18O values of the tufa carbonate differ by +0.6 to +1.0‰ from the calculated theoretical isotope composition (δ18OV-PDB) of lake water, indicating that the tufa also did not precipitate in isotopic equilibrium with ambient waters. Results show
that the greater the δ18O offset from the calculated, theoretical isotope composition of lake water for an ostracod species, the lower is its preferred
mean July temperature. Both our data and earlier published results on δ18O values in Holocene lacustrine carbonates and ostracods from north-eastern Europe, display pronounced decreases in δ18O with an increase in latitude of the study site. This suggests that temperature-dependent, and therefore latitude-dependent
isotopic composition of meteoric waters controlled the δ18O values in lacustrine tufa and ostracods throughout the Holocene. 相似文献
17.
为探究岩溶水库水文地球化学行为过程,对贵州普定夜郎湖表层水体进行了为期3 d的高分辨率昼夜监测。结果表明：1）多变的天气和水文条件叠加导致水体离子指标昼夜变化不显著,规律性较差。而水温、DO、pH值、SpC、SIc、pCO2等常规理化指标受水温变化和生物作用表现出明显的昼夜波动。2）利用亨利常数和主成分分析,得到温度变化、生物作用、人类活动、水库的蓄水与放水对夜郎湖水库水文地球化学特征变化的贡献率分别为21.66%、17.28%、14.08%和10.22%,说明作用于水库水文地球化学行为的因子具有多元性。3）δ 18O表现出与DO一致的波动趋势,即白天上升,晚上下降,反映在短时间尺度上,氢氧稳定同位素变化受控于生物过程（主要是呼吸作用过程）;而对比水库水体和大气降水的d-excess（d值）发现,水库水体的d值（8.21‰）显著偏低于当地大气降水的d值（9.64‰）,说明在长时间尺度上,主要受蒸发效应引起的不平衡分馏影响。 相似文献