首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到19条相似文献，搜索用时 156 毫秒
1.
蒸发岩是保存古环境信息的宝库,而石盐是蒸发岩盆地完全干涸后最主要的矿物。石盐矿物具有很好的封闭性,在浅埋深状态就会固结成岩,没有孔隙并且不可压缩。石盐、石膏、钙芒硝、芒硝中的包裹体,是潟湖或陆地盐湖环境下,通过蒸发而结晶析出过程中所捕获的流体(液体和/或气体)。因此,在石盐矿物的内部可以保存下来良好的原生石盐流体包裹体,它们记录了原始海洋/盐湖的温度、化学组分和大气成分的信息,为古环境研究提供了绝妙的直接记录。其中石盐原生流体包裹体的均一温度,可记录卤水沉积时的温度;浅水环境石盐流体包裹体记录的卤水温度近似等于气温。石盐原生流体包裹体中的卤水成分代表了海水/盐湖蒸发浓缩过程中的卤水,可通过其来推断当时的海水/盐湖水体的成分。石盐漏斗晶形成时是漂浮在卤水表面的,其原生流体包裹体可捕获当时的大气,而石盐是一种稳定的无机矿物,其原生流体包裹体可保存原始的大气信息。石盐原生流体包裹体可以提供其他传统地球化学手段无法提供的直接、精确、定量的地质记录,因此在未来的古环境研究中将成为焦点。  相似文献   

2.
徐洋  刘成林  曹养同 《地质学报》2021,95(7):2183-2192
古盐湖成盐演化具有多期次、连续性和淡化—咸化—盐化的周期性特征,系统研究成盐剖面的沉积韵律有利于恢复古盐湖成盐演化特征.本文以库车盆地KL4钻孔含盐系剖面及其74个石盐样品为研究对象,将含盐系剖面划分为4个成盐韵律,在此基础上开展岩相学、石盐元素地球化学以及石盐流体包裹体氢氧同位素分析等工作.结果显示:剖面上部Ⅲ和Ⅳ成盐韵律发育钾石盐、含钾石盐、杂卤石、钾石膏、钾芒硝等盐类矿物;K+含量的分布范围为0.021％～0.158％,平均含量0.051％;石盐原生流体包裹体中氢氧同位素δD和δ18 O值范围分别为-78.2‰～-58.7‰和-2.4‰～1.3‰,平均值分别为-66.32‰和-0.80‰.盐湖卤水从早期到晚期蒸发浓缩程度逐渐升高,早期成盐卤水在晚期高浓度卤水的形成过程扮演了预富集的角色,在Ⅲ和Ⅳ成盐阶段发现3次钾盐析出事件.本研究为探讨库车盆地中始新世古盐湖环境、沉积特征以及成盐规律提供了重要依据.  相似文献   

3.
罗布泊盐湖钙芒硝岩孔隙中蕴藏有超大型规模的卤水钾矿,富钾卤水成因一直备受关注。罗北凹地从统一的罗布泊大湖区中分隔出来后,成盐过程中其湖水仍以南部大湖的补给为主,罗北凹地卤水化学演化与"大耳朵"湖水密切相关。"大耳朵"湖区含石膏碎屑层普遍储藏有卤水,应该是罗北凹地盐湖的"源卤水",钾离子(ρ(K~+)为3.12 g/L左右)已初步富集,平均矿化度为198.83 g/L。为了查明该卤水的化学演化趋势及析盐序列,笔者于2009年、2010年两次采集了大量卤水样品,分别进行室内等温蒸发和自然蒸发实验。蒸发实验结果表明:随着卤水浓缩首先析出(硬)石膏,随后析出大量石盐,最后出现少量钾石盐和光卤石,与EQL/EVP卤水蒸发模型模拟结果相似。将碎屑层卤水蒸发过程中化学组成变化与罗北凹地卤水进行对比,结果显示罗布泊古湖水蒸发至石膏沉积之后,在罗北凹地水化学组成明显发生变化,没有大量石盐沉积,而以钙芒硝沉积为主。推测应是受到深部"富钙水"的持续补给,而"大耳朵"湖起到"预备盆地"的作用,罗布泊古湖水经"大耳朵"湖蒸发浓缩后,钾离子得到初步富集,在流入罗北凹地后与深部"富钙"水混合,强烈蒸发浓缩,大量钙芒硝矿物析出,最后形成富钾卤水。  相似文献   

4.
罗布泊卤水经室内恒温（30℃和52℃）蒸发结晶析出石盐，其内含有丰富的液相包裹体。测试这些石盐液相包裹体均一温度，发现仅有少量包裹体均一温度与石盐结晶卤水温度一致，大多数均一温度明显偏离结晶温度，大多数高出卤水温度约20℃～90℃，少数低于卤水温度约6℃～30℃，罗布泊盐湖自然沉积的石盐液相包裹体均一温度也存在类似情况，除少部分数据与当地卤水温度相近，大多也存在明显的差异。说明石盐包裹体均一温度可能受制于多个因数影响。因此，用石盐包裹体均一温度恢复沉积时期古水温或流体介质温度时，不能简单应用，需要综合分析才能从中提取可靠的地质信息。  相似文献   

5.
一里坪盐湖是柴达木盆地一个以富锂卤水为主的干盐湖,蕴藏有丰富的卤水钾锂资源,目前对成矿过程中卤水的成分及其演变规律方面的研究较少.论文选取一里坪盐湖中部钻孔HC2105岩芯的石盐为主要对象,利用激光剥蚀-电感耦合等离子质谱法开展了单个石盐原生流体包裹体成分分析,探讨恢复了一里坪盐湖地区晚更新世以来成盐期的古卤水成分.结果表明,一里坪盐湖下层石盐古卤水Li、B、K等离子浓度均高于上层石盐,这说明晚更新世成矿条件更好.古卤水中Li、B、K和Mg等离子具有正相关性,再结合对Ca离子浓度变化的研究,说明一里坪盐湖的主要物质来源为那棱郭勒河,深部卤水对其物质来源贡献较小;石盐流体包裹体中各离子浓度的演变规律与钻孔沉积韵律以及古气候变化三者基本可以拟合,从而证实盐湖卤水成分变化受到古气候变化的影响,干冷期可能更有利于富锂卤水矿的形成.  相似文献   

6.
复杂卤水组分对于石盐流体包裹体均一温度的影响尚不明确,文章基于NaCl-X-H_2O(X=KCl, MgCl_2,CaCl_2, Na_2SO_4)三元卤水体系,尝试探讨K~+、Mg~(2+)、Ca~(2+)、SO_4~(2-)对石盐流体包裹体均一温度测试结果的影响。不同卤水体系最大均一温度分析结果表明,K~+、Mg~(2+)、Ca~(2+)的存在总体上会导致石盐流体包裹体均一温度偏大,SO_4~(2-)的存在对均一温度的影响很小。以NaCl-H_2O体系为参照,NaCl-Na_2SO_4-H_2O体系平均均一温度较之要低,而NaCl-KCl-H_2O、NaCl-MgCl_2-H_2O和NaCl-CaCl_2-H_2O体系与其相反。NaCl-KCl-H_2O体系中的KCl浓度与平均均一温度呈现负相关关系,NaCl-MgCl_2-H_2O、NaCl-CaCl_2-H_2O、NaCl-Na_2SO_4-H_2O体系中的w(MgCl_2)、w(CaCl_2)和w(Na_2SO_4)与平均均一温度则呈现正相关关系。平均和最大均一温度分析结果都显示出复杂卤水体系中不同离子及其浓度对石盐流体包裹体均一温度会产生影响。本研究对于具有复杂化学组分卤水结晶析出石盐均一温度的研究具有重要的参考价值。  相似文献   

7.
基于海相石盐流体包裹体的古海水演化热力学模拟   总被引：2，自引：0，他引：2  
传统观点认为地质时期海水成分一成不变,然而包裹体测试技术的迅速发展,揭示出显生宙以来海水成分至少发生过两次大的旋回变化。本文基于世界多个海相沉积盆地的原生石盐包裹体实测数据,探讨了显生宙以来古海水地球化学、水化学类型、蒸发岩矿物组合特征的显著变化,并结合EQL/EVP卤水蒸发平衡模型,定量模拟了两种典型海水的蒸发演化过程、析盐规律和矿物组合特征,分析和探讨了中国海相沉积盆地的成钾前景。应用Spencer相图,揭示出在过去的600 Ma期间,古海水成分点在Cl-SO4和Ca-Cl两个相区内随时间发生周期性的震荡变化,志留纪、泥盆纪、侏罗纪和白垩纪的海水类型与现代海水迥然不同,为典型的Ca-Cl型水。Mg-2KSO4/Mg-Ca-2KJnecke相图分析结果显示,这些时期的石盐包裹体成分,位于富CaCl2、贫MgSO4的Mg-Ca-2K相图中光卤石、钾石盐稳定相区,指示原始海水相对于现代海水具有富Ca、贫Mg的特征,其析出的典型矿物组合主要有石盐、钾石盐、光卤石和溢晶石等。而新元古代、二叠纪和第三纪大部分石盐包裹体成分,都落到了Mg-2KSO4相图上的钾盐镁矾和钾石盐相区,和现代海水成分较为类似,具有富Mg2+、SO2-4的特征,其析出的典型矿物组合包括石盐、钾盐镁矾、硫镁矾、钾石盐和光卤石等。EQL/EVP定量模拟结果显示,富SO4-Mg型的海水和富CaCl型的古海水,蒸发演化路径和矿物析出序列截然不同,Ca-Cl型的海水更易形成优质钾盐矿床,有利的成钾时段为寒武纪-早石炭世、侏罗世-新生代早中期。  相似文献   

8.
柴达木盆地昆特依盐湖含杂卤石地层高分辨率矿物学研究   总被引：1，自引：0，他引：1  
柴达木盆地昆特依盐湖杂卤石资源丰富,是开展现代内陆盐湖杂卤石成因机制研究的良好载体.精细刻画沉积特征对阐释沉积矿床成因具有重要作用.本研究以昆特依盐湖大盐滩矿区ZK3608钻孔岩芯14.08-25.48 m段碎屑-杂卤石沉积韵律为研究对象,开展高分辨率矿物学研究,结合石盐流体包裹体化学组成和石盐中微量元素分析,尝试从高分辨率沉积学和矿物学的角度探讨杂卤石的成因.研究结果显示,石盐层产出的杂卤石含量低但分布范围广,为原生矿物;碎屑层中的杂卤石主要为次生矿物.石盐层与碎屑层之间存在一个过渡层位,该层位的杂卤石高度富集且矿物组成复杂,推测是由于原生与准同生杂卤石短时间内先后形成导致的.结合石盐流体包裹体化学组成所代表的古卤水变化特征分析表明,Ca-Cl型深部油田卤水的补给对研究区不同时期杂卤石的形成有重要影响.地球化学特征综合分析指示,石盐层的原生杂卤石由富钾镁的浓缩卤水与Ca-Cl型深部油田卤水混合直接生成;而过渡层位的杂卤石受到气候变化与Ca-Cl型深部油田卤水补给的共同作用.  相似文献   

9.
垫江凹陷位于四川盆地东部,是四川盆地三叠纪时期重要的成盐凹陷之一,但当时古卤水是否达到钾盐沉积阶段,是否具备形成海相钾盐的良好条件,一直存在争议。本文通过对垫江凹陷长平3井、高探1井和ZK001井嘉陵江组岩盐样品进行化学成分分析,以及对长平3井典型岩盐样品进行氯同位素分析来判断古卤水沉积阶段和成钾条件。结果发现垫江凹陷三叠系嘉陵江组岩盐δ37 Cl值均为负值,均小于-0.32‰,最低达到-1.18‰,绝大部分岩盐样品溴氯系数大于0.31,有很大一部分样品溴氯系数超过0.45,进一步表明垫江凹陷在嘉陵江期古卤水浓缩已达到钾石盐析出阶段,与岩盐包裹体成分分析结果一致。综合气候-物源-构造因素,认为垫江凹陷三叠纪嘉陵江期气候条件炎热,物质来源丰富,存在次级凹陷,古构造条件优越,具备良好的成钾潜力。  相似文献   

10.
在盐湖沉积演化过程中,钾镁盐在盐类矿物沉积的中晚期才开始结晶析出。因此,研究含盐系地层中盐类矿物的沉积地球化学特征,不仅可以从侧面获取岩盐的沉积物物质来源和成盐期古卤水蒸发浓缩程度等地球化学信息,而且可以直接揭示古盐湖期钾盐富集趋势及规律。目前,除在江陵凹陷的古近系沙市组等含盐系内发现了富钾卤水外,还在中-南部的钻孔盐矿盐岩中,发现了微量钾石盐和钾石膏,这些说明该凹陷古近纪具有成钾潜力。本文通过对SK3井蒸发岩特征研究及岩芯中K、Mg、Cl、Br离子含量与Br×103/Cl系数的垂向变化分析,揭示古盐湖浓缩演化与钾盐富集趋势,进一步揭示该层段沉积时期及所在凹陷古盐湖卤水钾的富集程度。  相似文献   

11.
Sichuan Basin is one of the most important marine–salt forming basins in China. The Simian and Triassic have a large number of evaporites. The Triassic strata have found a large amount of polyhalite and potassium-rich brine. However, no soluble potassium salt deposit were found. In this study, the halite in well Changping 3 which is located at the eastern part of the Sichuan basin was studied using the characteristics, hydrogen and oxygen isotopes of the fluid inclusion in halite to reconstruct the paleoenvironment. The salt rocks in well Changping 3 can be divided into two types: grey salt rock and orange salt rock. The result shows that the isotopic composition of the halite fluid inclusion is distinct from the global precipitation line reflecting that the salt formation process is under strong evaporation conditions and the climate is extremely dry. At the same time, compared with the hydrogen and oxygen isotopes of brine in the Sichuan Basin and the hydrous isotope composition of the inclusions in the salt inclusions of other areas in China, it is shown that the evaporation depth of the ancient seawater in the Sichuan Basin was high and reached the precipitation of potassium and magnesium stage.  相似文献   

12.
The Mengyejing potash deposit is located in the southern port of the Simao Basin, Yunnan Province, and is hosted in mid-Cretaceous strata. The chemical compositions of fluid inclusions in halite crystals, collected from the level-610 adit in the deposit, were analysed by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The results show that the brine is of the Na-K-Mg-Ca-Cl type and has K concentrations that are distinctly higher than those of Mg and Ca, unlike normal brines associated with Cretaceous halite. The high K concentrations indicate that the degree of evaporation of the ancient Mengyejing saline lake was very high, reaching the sylvite deposition stage but rarely reaching the carnallite deposition stage. The trajectory of the H and O isotopic compositions of the brines in the halite-hosted fluid inclusions corresponds to intense evaporation, indicating that the net evaporation exceeded the net inflow of brines. These brine compositions in halite-hosted fluid inclusions were likely formed by the dissolution of previously deposited K-bearing minerals by fresh continental and/or seawater, forming a type of modified seawater, with deep hydrothermal fluids potentially supplying additional potassium. The basin likely experienced multiple seawater incursion, dissolution and redeposition events in a high-temperature environment with high evaporation rates.  相似文献   

13.
The chemical evolution of seawater during the Phanerozoic is still a matter of debate. We have assembled and critically analyzed the available data for the composition of fluid inclusions in marine halite and for the mineralogy of marine evaporites. The composition of fluid inclusions in primary marine halite reveals two major long-term cycles in the chemistry of seawater during the past 600 myr. The concentration of Mg2+, Ca2+, and SO42− has varied quite dramatically. The Mg2+ concentration in seawater during most of the early Paleozoic and Jurassic to Cretaceous was as low as 30 to 40 mmol/kg H2O; it reached maximum values ≥50 mmol/kg H2O during the Late Neoproterozoic and Permian. The Ca2+ concentration in seawater during the Phanerozoic has reached maximum values two to three times greater than the concentration in seawater today (10.6 mmol/kg H2O), whereas SO42− concentrations may have been as low as 5 to 10 mmol/kg H2O (a third to a fifth of the modern value) during the Jurassic and Early Paleozoic. The Mg2+/Ca2+ ratio in seawater ranged from 1 to 1.5 during the early to middle Paleozoic and Jurassic-Cretaceous to a near-modern value of 5.2 during the Late Neoproterozoic and Permian. This change in seawater Mg2+/Ca2+ ratio is consistent with the notion of alternating “calcite-aragonite seas” recorded in oölites and marine carbonate cements.Several models have been proposed to explain the chemical evolution of seawater. These have invoked significant changes in one or more of the major geochemical processes that control the composition of seawater. The pattern and magnitude of the variations in the composition of seawater proposed in this study are similar to those proposed elsewhere that suggest that seawater fluxes through midocean ridges have played a major role in the evolution of seawater during the past 600 myr. Two Phanerozoic supercycles of the Earth’s exogenic processes were recognized in the literature that are caused by mantle convection and plate activity. The composition of seawater has apparently undergone dramatic secular changes in phase with these supercycles and as a consequence of biological evolution. Analyses of fluid inclusions containing unevaporated seawater and a better understanding of the processes that affect the composition of seawater are needed to refine our understanding of the history of Phanerozoic seawater.  相似文献   

14.
四川盆地三叠纪是主要的成钾期,目前发现的主要含钾矿物为杂卤石,有关早三叠世嘉陵江组四段石盐岩中杂卤石成因一直存在争议.采用薄片鉴定、扫描电镜、稀土元素和锶同位素等手段,分析了四川盆地东部垫江盐盆长寿地区嘉陵江组四段石盐岩中杂卤石矿物形态特征,初步探讨了该杂卤石成因及对寻找海相钾盐的指示意义.扫描电镜下与石盐岩共生的杂卤...  相似文献   

15.
Analyses of halogen concentration and stable chlorine isotope composition of fluid inclusions from hydrothermal quartz and carbonate veins spatially and temporally associated with giant unconformity-related uranium deposits from the Paleoproterozoic Athabasca Basin (Canada) were performed in order to determine the origin of chloride in the ore-forming brines. Microthermometric analyses show that samples contain variable amounts of a NaCl-rich brine (Cl concentration between 120,000 and 180,000 ppm) and a CaCl2-rich brine (Cl concentration between 160,000 and 220,000 ppm). Molar Cl/Br ratios of fluid inclusion leachates range from ∼100 to ∼900, with most values between 150 and 350. Cl/Br ratios below 650 (seawater value) indicate that the high salinities were acquired by evaporation of seawater. Most δ37Cl values are between −0.6‰ and 0‰ (seawater value) which is also compatible with a common evaporated seawater origin for both NaCl- and CaCl2-rich brines.Slight discrepancies between the Cl concentration, Cl/Br, δ37Cl data and seawater evaporation trends, indicate that the evaporated seawater underwent secondary minor modification of its composition by: (i) mixing with a minor amount of halite-dissolution brine or re-equilibration with halite during burial; (ii) dilution in a maximum of 30% of connate and/or formation waters during its migration towards the base of the Athabasca sandstones; (iii) leaching of chloride from biotites within basement rocks and (iv) water loss by hydration reactions in alteration haloes linked to uranium deposition.The chloride in uranium ore-forming brines of the Athabasca Basin has an unambiguous dominantly marine origin and has required large-scale seawater evaporation and evaporite deposition. Although the direct evidence for evaporative environments in the Athabasca Basin are lacking due to the erosion of ∼80% of the sedimentary pile, Cl/Br ratios and δ37Cl values of brines have behaved conservatively at the basin scale and throughout basin history.  相似文献   

16.
四川盆地是我国重要的成盐盆地,但是否能形成一定规模的钾盐矿床一直存在争议。本文以四川盆地三叠纪杂卤石成因-海相钾盐成钾条件分析-次级凹陷圈定-钾盐成钾靶区圈定为主线,利用光薄片鉴定、扫描电镜、Sr同位素、大地电磁测深及地震解译等手段分析了四川盆地三叠纪钾盐成矿潜力,并进行了资源量预测。四川盆地东部早三叠世嘉陵江期岩盐中赋存的杂卤石是自生的,是海水高度浓缩的产物,暗示岩盐沉积时古卤水浓缩已达到钾镁盐析出阶段,长寿双龙-合兴一带和垫江董家场一带可能存在有利于钾盐沉积的次级凹陷,后期构造运动对钾盐改造较小,保存条件较好。利用地震解释和大地电磁测深等结果初步圈定了长寿双龙-保合村勘查靶区,估算了资源量,为开展钻孔验证提供了科学依据。  相似文献   

17.
Halite possesses great potential for hosting and storing information vital to the reconstruction of Earth's ancient climate, seawater chemistry and evolving atmosphere. Here, we propose a screening protocol that not only distinguishes between primary and secondary halite, but also identifies fluid inclusions that carry original gas trapped during the primary crystallization process. An integrated multi-analytical protocol is presented for sample preparation, petrographic evaluation, analytical measurements and distinguishing original gases and contents from contaminants. The screening protocol starts with the visual inspection of halite for primary chevron and hopper features and/or milky appearance. Then, petrography is used to distinguish between primary and secondary (diagenetic) crystal fabrics and inclusions. The trace element and isotope geochemistry speak directly to the composition of the depositional and/or diagenetic fluids and to the formation in marine, non-marine or diagenetic settings. Furthermore, rare earth elements and redox sensitive elements may address the redox conditions of the salt pan/flat brines, whereas microthermometry helps characterize the depositional/diagenetic environment's temperature. Finally, gas extracted by quadrupole mass-spectrometer from gas bubbles in fluid inclusions is screened with concomitant CH4, CO2 and Ar contents to distinguish and quantify organic matter decomposition contributions and with 40Ar/36Ar to monitor modern atmospheric gas diffusion/leakage issues, and thus, contamination of the primary gas contents.Our test case shows that halite collected from cores is well-suited in maintaining its original mineralogical texture, chemistry and gas content. Our integrated screening protocol suggests that the 815 Myr old halite from the Tonian Browne Formation of the Officer Basin, Australia formed under atmospheric conditions of about 10.9% pO2 (back calculation) or 9.6% pO2 (mean calculation). The coeval Neoproterozoic gypsum collected in outcrop from Minto Inlet, Victoria Island, Canada underwent some mineralogical alteration. However, experiments suggest that depositional gypsum from outcrop/core may have potential of retaining vestiges of original gas in fluid inclusions.  相似文献   

18.
锶同位素已经成为全球海平面变化、造山运动、古气候和古环境等全球地质事件研究与对比的有效工具之一。本文以四川盆地东部地区早中三叠世蒸发岩的野外剖面和钻孔岩心为主要研究对象,测试了碳酸盐岩、硫酸盐岩和石盐岩的锶同位素组成,并建立了相应的锶同位素演化曲线。研究结果显示,碳酸盐岩的87Sr/86Sr值平均为0.707 895,硬石膏岩的87Sr/86Sr值平均为0.708 174,石盐岩的87Sr/86Sr值平均为0.708 177,同时碳酸盐岩的87Sr/86Sr值从早三叠世的0.707 413快速增加到中三叠世早期的0.708 515,而后呈现下降趋势。从总体上看,这些87Sr/86Sr值与全球早中三叠世同期的87Sr/86Sr值数据接近,说明四川盆地东部地区早中三叠世钾盐的物质来源大部分为海水,并沉积于海相沉积环境,同时由于火山...  相似文献   

19.
One-hundred fluid inclusions in Silurian marine halite were analyzed in order to determine the major-ion composition of Silurian seawater. The samples analyzed were from three formations in the Late Silurian Michigan Basin, the A-1, A-2, and B Evaporites of the Salina Group, and one formation in the Early Silurian Canning Basin (Australia), the Mallowa Salt of the Carribuddy Group. The results indicate that the major-ion composition of Silurian seawater was not the same as present-day seawater. The Silurian ocean had lower concentrations of Mg2+, Na+, and SO42−, and much higher concentrations of Ca2+ relative to the ocean’s present-day composition. Furthermore, Silurian seawater had Ca2+ in excess of SO42−. Evaporation of Silurian seawater of the composition determined in this study produces KCl-type potash minerals that lack the MgSO4-type late stage salts formed during the evaporation of present-day seawater. The relatively low Na+ concentrations in Silurian seawater support the hypothesis that oscillations in the major-ion composition of the oceans are primarily controlled by changes in the flux of mid-ocean ridge brine and riverine inputs and not global or basin-scale, seawater-driven dolomitization. The Mg2+/Ca2+ ratio of Silurian seawater was ∼1.4, and the K+/Ca2+ ratio was ∼0.3, both of which differ from the present-day counterparts of 5 and 1, respectively. Seawaters with Mg2+/Ca2+ <2 facilitate the precipitation of low-magnesian calcite (mol % Mg < 4) marine ooids and submarine carbonate cements whereas seawaters with Mg2+/Ca2+ >2 (e.g., modern seawater) facilitate the precipitation of aragonite and high-magnesian calcite. Therefore, the early Paleozoic calcite seas were likely due to the low Mg2+/Ca2+ ratio of seawater, not the pCO2 of the Silurian atmosphere.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号