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1.
《Gondwana Research》2014,25(3):1070-1089
The Ediacaran–Cambrian was one of the most important periods for the evolution of life. Recent studies have provided detailed chemostratigraphies that decipher the linkages between ambient surface environmental changes and biological evolution. The occurrence of skeletal fossils in Ediacaran rocks suggests that the possible onset of Ca-biomineralization started in the latest Neoproterozoic. Molecular clocks also predict the emergence of animals containing Ca-carbonate spicules in the Neoproterozoic. Therefore, it is important to estimate the transition of the Ca cycle in seawater. Ancient Ca cycles in the oceans are estimated from the calcium isotopic compositions of carbonate rocks. However, the lack of continuous Ca isotopic data in the Ediacaran leaves the Ca cycle unresolved.The almost continuously exposed, Ediacaran and Cambrian strata in South China mainly comprise carbonate rocks with subordinate black shales and sandstones, which contain many fossils, suitable for the study of environmental and biological changes. We conducted drilling from the Liantuo, via the Nantuo, Doushantuo, Dengying and Yanjiahe to the Shuijingtuo formation at four sites in the Three Gorges area in order to obtain continuous, fresh samples without surface alteration and oxidation. We analyzed 44Ca/42Ca ratios in carbonate rocks with a multiple collector-inductively coupled plasma-mass spectrometer (MC-ICP-MS) screened for diagenetic alteration.The resultant δ44/42Ca ratios exhibit a smooth curve. The values of δ44/42Ca are anomalously high relative to those in the Phanerozoic, and they gradually decrease towards the end of the Ediacaran. Our new Ca isotope chemostratigraphy suggests that a different Ca cycle had existed during the Ediacaran. The long-term, high δ44/42Ca is not simply explicable by changes in temperature, differences in carbonate mineralogy, or changes in the input/output fluxes of Ca to the ocean. We propose three possible explanations for the observed high δ44/42Ca ratios in the Ediacaran: high δ44/42Ca ratios of Ca inputs, potential undiscovered sinks of Ca with low δ44/42Ca values, and negligible isotope fractionation between carbonate and seawater; we consider that one or all of these contributed to the high δ44/42Ca ratios. Of these, we prefer the small isotope fractionation, which implies that the Ca concentration in seawater was initially low in the early Ediacaran and increased throughout that period.  相似文献   

2.
We report mass‐independent and mass‐dependent Ca isotopic compositions for thirteen geological reference materials, including carbonates (NIST SRM 915a and 915b), Atlantic seawater as well as ten rock reference materials ranging from peridotite to sandstone, using traditional ε and δ values relative to NIST SRM 915a, respectively. Isotope ratio determinations were conducted by independent unspiked and 43Ca‐48Ca double‐spiked measurements using a customised Triton Plus TIMS. The mean of twelve measurement results gave ε40/44Ca values within ± 1.1, except for GSP‐2 that had ε40/44Ca = 4.04 ± 0.15 (2SE). Significant radiogenic 40Ca enrichment was evident in some high K/Ca samples. At an uncertainty level of ± 0.6, all reference materials had the same ε43/44Ca and ε48/44Ca values. We suggest the use of δ44/42Ca to report mass‐dependent Ca isotopic compositions. The precision under intermediate measurement conditions for δ44/42Ca over eight months in our laboratory was ± 0.03‰ (with n ≥ 8 repeat measurements). Measured igneous reference materials gave δ44/42Ca values ranging from 0.27‰ to 0.54‰. Significant Ca isotope fractionation may occur during magmatic and metasomatism processes. Studied reference materials with higher (Dyn/Ybn) tend to have lower δ44/42Ca, implying a potential role of garnet in producing magmas with low δ44/42Ca. Sandstone GBW07106 had a δ44/42Ca value of 0.22‰, lower than all igneous rocks studied so far.  相似文献   

3.
Calcium isotopic compositions of sixteen Ca‐bearing USGS geological reference materials including igneous and sedimentary rocks are reported. Calcium isotopic compositions were determined in two laboratories (GPMR, State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Wuhan; and CIG, Centre for Isotope Geochemistry, University of California, Berkeley) using the 42Ca‐48Ca double‐spike technique by thermal ionisation mass spectrometry. As opposed to common cation exchange resin, a micro‐column filled with Ca‐selective resin (DGA resin) was used in order to achieve high recovery (> 96%) and efficient separation of Ca from the sample matrix. The intermediate measurement precision was evaluated at 0.14‰ (2s) for δ44/40CaSRM915a at GPMR, based on replicate measurements of pure Ca reference material NIST SRM 915a, NIST SRM 915b and seawater. Overall, the measurement uncertainties in both laboratories were better than 0.15‰ at the 2s level. Result validation was carried out for all available data sets. The Ca isotopic compositions of USGS reference materials are not only in agreement between GPMR and CIG, but also in agreement with previously published data within quoted uncertainties. The comprehensive data set reported in this study serves as a reference for both quality assurance and interlaboratory comparison of high precision Ca isotopic study.  相似文献   

4.
The calcium isotopic composition of NIST SRM 915b and 1486 provided by the National Institute of Standards and Technology was analysed. The δ44/40Ca values of the two reference materials relative to NIST SRM 915a were: NIST SRM 915b =+0.72 ± 0.04‰ and NIST SRM 1486 =?1.01 ± 0.02‰. NIST SRM 1486 did not require any chemical separation prior to measurement.  相似文献   

5.
Phosphate deposits of the Ediacaran Doushantuo Formation accumulated in the central Guizhou Province are the typical phosphate-rich sediments during the Neoproterozoic Phosphogenic Episodes,which occurred after the “Snowball Earth”period and Neoproterozoic Oxygenation Event. However,the mechanisms of phosphate enrichment in seawater have always been hotly debated,and the research for correlations between phosphogenesis and transition of Ediacaran palaeo-ocean environments is still unsubstantial. This study focused on the sedimentological,petrological,mineralogical and geochemical analyses on the Doushantuo pristine phosphorite in Weng'an,Zunyi and Danzhai area. Documented by spherulitic phosphorites in the Lower Phosphorite beds from Weng'an area that contain abundant autogenetic Fe-bearing minerals such as pyrite and glauconite and show weak Ce negative anomaly,Fe-redox pumping in low-oxygen environments are the important phosphogenesis mechanism but only limited in coastal waters in the Early Doushantuo Period. Phosphorite in the Upper Phosphorite beds deposited within organic-rich beds and contain massive biological fossils suggests that phosphogenesis might have been triggered by degradation of organic matter and biological action in the Late Doushantuo Period,and distribution of phosphatic sediments extended to the deeper shelf to slope setting. Obvious Ce negative anomaly implies the increase of oxygen content in seawater. The transition of phosphogenesis mechanisms and the expansion of phosphorite deposits are the sedimentary response of ocean oxygenation,and the associated evolution of metazoans also changed the redox conditions of the deep seawater. These sedimentary and geochemistry data reflect the closed coupling relation between Doushantuo phosphorite in Guizhou Province and the Neoproterozoic Oxygenation Event.  相似文献   

6.
We report δ44/40Ca(SRM 915a) values for eight fused MPI‐DING glasses and the respective original powders, six USGS igneous rock reference materials, the U‐Th disequilibria reference material TML, IAEA‐CO1 (Carrara marble) and several igneous rocks (komatiites and carbonatites). Sample selection was guided by three considerations: (1) to address the need for information values on reference materials that are widely available in support of interlaboratory comparison studies; (2) support the development of in situ laser ablation and ion microprobe techniques, which require isotopically homogenous reference samples for ablation; and (3) provide Ca isotope values on a wider range of igneous and metamorphic rock types than is currently available in the scientific literature. Calcium isotope ratios were measured by thermal ionisation mass spectrometry in two laboratories (IFM‐GEOMAR and Saskatchewan Isotope Laboratory) using 43Ca/48Ca‐ and 42Ca/43Ca‐double spike techniques and reported relative to the calcium carbonate reference material NIST SRM 915a. The measurement uncertainty in both laboratories was better than 0.2‰ at the 95% confidence level. The impact of different preparation methods on the δ44/40Ca(SRM 915a) values was found to be negligible. Except for ML3‐B, the original powders and the respective MPI‐DING glasses showed identical δ44/40Ca(SRM 915a) values; therefore, possible variations in the Ca isotope compositions resulting from the fusion process are excluded. Individual analyses of different glass fragments indicated that the glasses are well homogenised on the mm scale with respect to Ca. The range of δ44/40Ca(SRM 915a) values in the igneous rocks studied was larger than previously observed, mostly owing to the inclusion of ultramafic rocks from ophiolite sections. In particular, the dunite DTS‐1 (1.49 ± 0.06‰) and the peridotite PCC‐1 (1.14 ± 0.07‰) are enriched in 44Ca relative to volcanic rocks (0.8 ± 0.1‰). The Carrara marble (1.32 ± 0.06‰) was also found to be enriched in 44Ca relative to the values of assumed precursor carbonates (< 0.8‰). These findings suggest that the isotopes of Ca are susceptible to fractionation at high temperatures by, as yet, unidentified igneous and metamorphic processes.  相似文献   

7.
Calcium Isotopic Composition of Various Reference Materials and Seawater   总被引：1，自引：0，他引：1  
A compilation of δ44/40Ca (δ44/40Ca) data sets of different calcium reference materials is presented, based on measurements in three different laboratories (Institute of Geological Sciences, Bern; Centre de Géochimie de la Surface, Strasbourg; GEOMAR, Kiel) to support the establishment of a calcium isotope reference standard. Samples include a series of international and internal Ca reference materials, including NIST SRM 915a, seawater, two calcium carbonates and a CaF2 reference sample. The deviations in δ44/40Ca for selected pairs of reference samples have been defined and are consistent within statistical uncertainties in all three laboratories. Emphasis has been placed on characterising both NIST SRM 915a as an internationally available high purity Ca reference sample and seawater as representative of an important and widely available geological reservoir. The difference between δ44/40Ca of NIST SRM 915a and seawater is defined as -1.88 O.O4%o (δ44/42CaNISTSRM915a/Sw= -0.94 0.07%o). The conversion of values referenced to NIST SRM 915a to seawater can be described by the simplified equation δ44/40CaSa/Sw=δ44/40CaSa/NIST SRM 915a - 1.88 (δ44/42CaSa/Sw=δ44/42CaSa/NIST SRM 915a - 0.94). We propose the use of NIST SRM 915a as general Ca isotope reference standard, with seawater being defined as the major reservoir with respect to oceanographic studies.  相似文献   

8.
High‐precision calcium isotopic compositions of a set of geological reference materials from the IAG (OU‐6), ANRT (UB‐N), MPI‐DING, USGS and GSJ, relative to NIST SRM 915a, are reported here. Measurements were performed by thermal ionisation mass spectrometry (Triton instrument) using a 42Ca–43Ca double spike. δ44/40Ca values of selected reference materials, mainly felsic rocks, are reported for the first time. Felsic rock values of δ44/40Ca ranged from 0.13‰ to 1.17‰, probably implying Ca isotopic fractionation could occur during magma evolution. δ44/40Ca values of ultramafic rocks, ranging from 0.74‰ to 1.51‰, were positively correlated with MgO and negatively with CaO contents, possibly owing to Ca isotopic fractionation during partial melting. δ44/40Ca of intermediate‐mafic rocks were around 0.78‰ and displayed limited variation, suggesting Ca isotopic fractionation is insignificant during magma evolution processes. As expected, δ44/40Ca of sedimentary and metamorphic rocks varied widely due to complex geological processes.  相似文献   

9.
The Neoproterozoic Sete Lagoas Formation (ca 610 Ma) of the São Francisco Basin, Brazil, is a succession of siltstone, limestone and phosphorite. Phosphorite forms part of a previously unrecognized 150 to 200 m thick, unconformity bounded depositional sequence. Lithofacies stacking patterns indicate that deposition was punctuated by higher order fluctuations in base level that produced aggradational parasequences. These shallowing‐upward cycles record the progradation of phosphate‐rich intertidal flats over shallow subtidal deposits as accommodation filled. The presence of mudcracks, authigenic chert nodules, lack of coarse terrigenous clastics and the abundance of silt with fine, abraded quartz grains suggests accumulation along an arid coastline with significant aeolian input. Delivery of phosphorus adsorbed on aeolian Fe‐(oxyhydr)oxide and clay is interpreted as having stimulated phosphogenesis in peritidal environments. Lithofacies associations indicate that windblown phosphorus promoted the establishment of cyanobacterial communities along the coast, which produced photosynthetic oxygen and the suboxic conditions necessary for the precipitation of authigenic carbonate fluorapatite. As in other Precambrian phosphatic systems, nearshore oxygen oases were a prerequisite for phosphorite accumulation because redox sensitive phosphogenic processes were pushed into the sediment to concentrate phosphorus. In more distal, anoxic environments phosphorite could not form because these biotic and abiotic processes were suspended in the water column, which cycled phosphorus in sea water rather than at the sediment–water interface. Such shallow‐water phosphorite is unlike larger, younger Neoproterozoic–Phanerozoic phosphatic deposits inferred to have formed in deeper‐upwelling related environments. The increasing size of phosphatic deposits through the latest Precambrian is interpreted as reflecting the progressive ventilation of the oceans during the Neoproterozoic Oxygenation Event, and resultant expansion of phosphogenic environments into distal settings. The widespread cycling of bioavailable phosphorus at the sea floor not only produced the first true phosphorite giants, but may have also been an important precondition for the evolution of multicellular animals.  相似文献   

10.
A proposal is made to standardise the reporting of Ca isotope data to the δ44Ca/40Ca notation (or δ44Ca/42Ca) and to adopt NIST SRM 915a as the reference standard.  相似文献   

11.
近年来,随着风暴流和风暴岩的新理论、新概念的不断引入,在分析沉积环境、沉积成矿作用时,不断提出了许多新思路,也不断地冲击和修正以往的传统认识,作者于1986年随同成都地矿所寒武系磷矿专题组对滇东一带包括昆阳梅树村、海口、鸣矣河、晋宁王家湾、二街、八街、安宁白登、江川清水沟、宜良大滴水、寻甸先锋等矿区的磷矿进行了详细的研究,在下寒武统中谊村段及其相当的地层中发现了多层磷质风暴沉积物。本文拟概略介绍磷质风暴沉积物的标志、特征、剖面结构并初步探讨磷矿富集与风暴事件关系的沉积演化模式。  相似文献   

12.
The calcium-isotope composition (δ44/42Ca) was analyzed in modern, Cretaceous and Carboniferous marine skeletal carbonates as well as in bioclasts, non-skeletal components, and diagenetic cements of Cretaceous and Carboniferous limestones. In order to gain insight in Ca2+aq-CaCO3-isotope fractionation mechanisms in marine carbonates, splits of samples were analyzed for Sr, Mg, Fe, and Mn concentrations and for their oxygen and carbon isotopic composition. Biological carbonates generally have lower δ44/42Ca values than inorganic marine cements, and there appears to be no fractionation between seawater and marine inorganic calcite. A kinetic isotope effect related to precipitation rate is considered to control the overall discrimination against 44Ca in biological carbonates when compared to inorganic precipitates. This is supported by a well-defined correlation of the δ44/42Ca values with Sr concentrations in Cretaceous limestones that contain biological carbonates at various stages of marine diagenetic alteration. No significant temperature dependence of Ca-isotope fractionation was found in shells of Cretaceous rudist bivalves that have recorded large seasonal temperature variations as derived from δ18O values and Mg concentrations. The reconstruction of secular variations in the δ44/42Ca value of seawater from well preserved skeletal calcite is compromised by a broad range of variation found in both modern and Cretaceous biological carbonates, independent of chemical composition or mineralogy. Despite these variations that may be due to still unidentified biological fractionation mechanisms, the δ44/42Ca values of Cretaceous skeletal calcite suggest that the δ44/42Ca value of Cretaceous seawater was 0.3-0.4‰ lower than that of the modern ocean.  相似文献   

13.
Calcium isotopes in tissues are thought to be influenced by an individual’s diet, reflecting parameters such as trophic level and dairy consumption, but this has not been carefully assessed. We report the calcium isotope ratios (δ44/42Ca) of modern and archaeological animal and human bone (n = 216). Modern sheep raised at the same location show 0.14 ± 0.08‰ higher δ44/42Ca in females than in males, which we attribute to lactation by the ewes. In the archaeological bone samples the calcium isotope ratios of the herbivorous fauna vary by location. At a single site, the archaeological fauna do not show a trophic level effect. Humans have lower δ44/42Ca than the mean site fauna by 0.22 ± 0.22‰, and the humans have a greater δ44/42Ca range than the animals. No effect of sex or age on the calcium isotope ratios was found, and intra-individual skeletal δ44/42Ca variability is negligible. We rule out dairy consumption as the main cause of the lower human δ44/42Ca, based on results from sites pre-dating animal domestication and dairy availability, and suggest instead that individual physiology and calcium intake may be important in determining bone calcium isotope ratios.  相似文献   

14.
贵州瓮安磷矿陡山沱组地层元素地球化学特征   总被引：2，自引：0，他引：2  
瓮安陡山沱组上磷矿层含有大量早期多细胞动物化石(瓮安生物群),而陡山沱组下磷矿层未发现该生物群,说明上下两个磷矿层体现了不同的沉积环境。上磷矿层的氧化还原敏感元素Mo,U,V含量较下磷矿层要低很多。底部白云岩层、下磷矿层和中部白云岩层,无Ce异常,而上磷矿层和灯影组白云岩层Ce为负异常。这些表明,瓮安陡山沱组地层形成的海水沉积环境由下部的缺氧环境向上部的氧化环境转变。  相似文献   

15.
新元古代末期历经“雪球地球”和大气、海洋增氧事件后,发生了全球性成磷事件,贵州省震旦系陡山沱组大规模磷矿床沉积是本次成磷事件的典型代表。然而现阶段对贵州陡山沱组磷块岩成磷作用机制研究存在诸多争议,成磷事件与同期古海洋环境转变之间的关联研究也较为薄弱。作者以贵州省瓮安、遵义和丹寨地区陡山沱组原生磷块岩为研究对象开展的沉积学、岩石学、矿物学和地球化学特征研究表明: 陡山沱早期成磷作用被限制在浅水海岸,瓮安地区A矿层球粒磷块岩中大量的含铁自生矿物黄铁矿、海绿石以及无Ce负异常指示的贫氧沉积水体环境均表明,Fe-氧化还原泵成磷模式在富磷过程中发挥了重要作用;陡山沱晚期磷块岩分布扩散至较深水陆棚—斜坡沉积相区,磷块岩与富有机质岩层共生,矿物晶体形态特征与矿石内富含的大量生物化石均表明,有机质沉降聚磷作用和生物成磷作用促使磷块岩大量沉积,较明显的Ce负异常值也指示了海水氧气含量的提升。成磷作用模式的转变和磷块岩分布的扩展是对海洋增氧事件的沉积响应,同时造成的多细胞动物演化也影响了深部水体的氧化还原状态,进而反映了贵州省陡山沱组磷块岩大规模沉积与新元古代末期氧化事件(NOE)密切的耦合关系。  相似文献   

16.
郑荣才  文华国  郑超  罗平  李国军  陈守春 《岩石学报》2009,25(10):2459-2468
研究了川东北普光气田下三叠统飞仙关组白云岩储层的岩石结构Sr的含量和Sr同位素组成,讨论了它的成因,飞仙关组优质储层为成岩期埋藏交代白云化作用的产物,来自岩石结构和Sr同位素和Sr含量的证据包括如下几个方面:(1)与准同生白云岩比较,埋藏白云岩的岩石结构和Sr同位素和Sr含量地球化学特征与前者有显著差别;(2)飞仙关组所有各类碳酸盐岩(或矿物)具有早三叠世海水Sr同位素组成特征,~(87)Sr/~(86)Sr比值变化范围为0.706588～0.708187,覆盖了全球早三叠世海水Sr同位素的变化范围(0.7076～0.7078),平均值0.707656与全球早三叠世平均值(0.707743)基本一致;(3)埋藏白云岩~(87)Sr/86Sr比值变化范围为0.707122～0.707419,平均值0.707421,都略低于全球早三叠世海水Sr同位素变化范围和平均值,但与已报道的川东北早三叠世飞仙关期海水Sr同位素变化范围(0.707330～0.707383)和平均值(0.707350)都非常接近,说明白云石化流体具有强烈的川东北地区早三叠世飞仙关期海水Sr同位素组成特征;(4)综合岩石结构、Sr同位素和Sr含量地球化学特征,证明飞仙关组白云岩储层为成岩期埋藏交代作用产物,白云石化流体来自地层中高Sr和高盐度的海源地层水.  相似文献   

17.
Fluoride analyses display downward decreasing pore water gradients in Peru shelf phosphatic muds that require diffusion from the overlying seawater into the sediment column and removal by reaction within the upper few tens of centimeters, presumably by incorporation into carbonate fluorapatite. The profiles can be modeled as first-order F-removal with rate constants of ~3 yr?1 and asymptotic F-concentrations deep in the cores of 35–45 μM, almost one-half the seawater value. The integrated flux of fluoride from seawater into organic-rich shelf sediments in coastal-upwelling zones (phosphatic muds) yields a contemporaneous global F-burial of 0.54 × 1010 mol-F yr?1, about one-fifth the burial in other sinks (mostly carbonates and opal). The associated burial flux of phosphorus in shelf phosphorites is about 1.6 × 1010 mol-P yr?1, comparable to P-burial in the deep sea with organic matter (~1.4 × 1010 mol yr?1) and biogenic carbonates (~1.4 × 1010 mol yr?1). Thus phosphorite formation on the Peru shelf is a significant contemporaneous process.  相似文献   

18.
磷块岩形成过程中的生物作用   总被引：3，自引：1，他引：3       下载免费PDF全文
 对我国震旦纪、寒武纪磷块岩矿床的研究表明,参与成磷作用的生物主要是菌、藻类微生物。生物作用的标志表现为:P2O5主要富集在叠层石磷块岩中,富集在叠层石的柱体上,富集在柱体内部的富藻纹层中;而与磷块岩共生的白云石和黄铁矿的δ13C值和δ34S值相对均较低,则是生物参与成磷作用的同位素标志特点。生物的成磷作用贯穿成磷过程的始终,但它随作用的相带、环境和阶段不同,生物的种属和作用方式也不同,因而矿石和矿床的质量也随之而异。  相似文献   

19.
An 18 million year record of the Ca isotopic composition (δ44/42Ca) of planktonic foraminiferans from ODP site 925, in the Atlantic, on the Ceara Rise, provides the opportunity for critical analysis of Ca isotope-based reconstructions of the Ca cycle. δ44/42Ca in this record averages +0.37 ± 0.05 (1σ SD) and ranges from +0.21‰ to +0.52‰. The record is a good match to previously published Neogene Ca isotope records based on foraminiferans, but is not similar to the record based on bulk carbonates, which has values that are as much as 0.25‰ lower. Bulk carbonate and planktonic foraminiferans from core tops differ slightly in their δ44/42Ca (i.e., by 0.06 ± 0.06‰ (n = 5)), while the difference between bulk carbonate and foraminiferan values further back in time is markedly larger, leaving open the question of the cause of the difference. Modeling the global Ca cycle from downcore variations in δ44/42Ca by assuming fixed values for the isotopic composition of weathering inputs (δ44/42Caw) and for isotope fractionation associated with the production of carbonate sediments (Δsed) results in unrealistically large variations in the total mass of Ca2+ in the oceans over the Neogene. Alternatively, variations of ±0.05‰ in the Ca isotope composition of weathering inputs or in the extent of fractionation of Ca isotopes during calcareous sediment formation could entirely account for variations in the Ca isotopic composition of marine carbonates. Ca isotope fractionation during continental weathering, such as has been recently observed, could easily result in variations in δ44/42Caw of a few tenths of permil. Likewise a difference in the fractionation factors associated with aragonite versus calcite formation could drive shifts in Δsed of tenths of permil with shifts in the relative output of calcite and aragonite from the ocean. Until better constraints on variations in δ44/42Caw and Δsed have been established, modeling the Ca2+ content of seawater from Ca isotope curves should be approached cautiously.  相似文献   

20.
《Gondwana Research》2006,9(4):579-584
A first report of discovery of spherules, glassy balls, highly magnetic fine dust and microbracciated matrix in the Fatehgarh Formation of Barmer Basin, Rajasthan, India is being presented in this paper. The Fatehgarh Formation is a mixed siliciclastic, carbonate and phosphorite formation of Cretaceous age in the Barmer Basin that comprises sediments of Middle Jurassic to Lower Eocene age. The phosphorite zone in the Fatehgarh Formation is ∼8 metre-thick zone that comprises phosphatic sandstone, bone bed, bedded phosphorite and phosphatic and non phosphatic gastropod beds. The spherules occur in a thin phosphatic-clay mud and silt band of bone bed, which also yielded a very rich and diverse microvertebrate assemblage with a dominant Late Cretaceous (Maastrichtian) form of Igdabatis along with forms comprising of Semionodontid, Lapisosteum and Enchodontid. The end Cretaceous is marked for a mass extinction of numerous species including dinosaurs. An extraterrestrial impact is interpreted as the reason for this mass extinction. Whether these spherules are related to the volcanic source or K/T Boundary impact ejecta found at Caribbean and Gulf of Mexico region needs detailed chemical and age characterization for which study is in progress.  相似文献   

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