The Silurian of Gotland (Sweden): facies interpretation based on stable isotopes in brachiopod shells

The Silurian of Gotland, Sweden, consists of 440 m of carbonate deposits. Repeatedly, uniform sequences of micritic limestones and marls are interrupted by complex-structured reefs and by adjacent platform sediments. Generally, the alteration of facies is interpreted as the result of sea-level fluctuations caused by a gradual regression with superimposed minor transgressive pulses. The purpose of this study is a facies interpretation based on both field observations and stable isotope measurements of brachiopod shells. Approximately 700 samples from stratigraphically arranged localities in different facies areas have been investigated. The carbon and oxygen isotopes show principally parallel curves and a close relationship to the stratigraphic sequence. Lower values occur in periods dominated by deposition of marly sequences. Higher values are observed in periods dominated by reefs and extended carbonate platforms. The oxygen isotope ratios are interpreted to reflect paleosalinity changes due to varying freshwater input, rather than to paleotemperature. Carbon isotope ratios are believed to have been connected to global changes in the burial of organic carbon in black shales during periods of euxinic deep water conditions. Consequently, the facies succession on Gotland results from global paleoclimatic conditions. Changes in terrigenous input due to different rates of weathering and freshwater runoff, rather than sea-level fluctuations, control the carbonate formation of the Silurian on Gotland.     

Origin of facies zonation in microbial carbonate platform slopes: Clues from trace element and stable isotope geochemistry (Middle Triassic,Dolomites, Italy)

Limestones containing radiaxial fibrous cements were sampled along the southern slope of the late Anisian (Middle Triassic) Latemar carbonate platform in the Dolomites, northern Italy. The Latemar upper slopes comprise massive microbial boundstone, whereas lower slopes are made of clinostratified grainstone, rudstone and breccia. Samples are representative of a seawater column from near sea‐level to an aphotic zone at about 500 m water depth. Radiaxial fibrous cements were analyzed for carbon (δ¹³C) and oxygen (δ¹⁸O) stable isotopic composition, as well as major and trace element content, to shed light on the origin of the slope facies zonation. The δ¹³C vary between 1·7‰ and 2·3‰ (Vienna Pee‐Dee Belemnite), with lowest values at palaeo‐water depths between 70 m and 300 m. Radiaxial fibrous cements yielded seawater‐like rare earth element patterns with light rare earth element depletion (Nd_SN/Yb_SN ≈ 0·4), superchondritic yttrium/holmium ratios (≈55) and negative cerium anomalies. Cadmium reaches maximum values of ca 0·5 to 0·7 μg/g at palaeo‐water depths between 70 m and 300 m; barium contents (0·8 to 1·8 μg/g) increase linearly with depth. The downslope patterns of δ¹³C and cadmium suggest increased nutrient and organic matter contents at depths between ca 70 m and 300 m and point to an active biological pump. The peak in cadmium and the minimum of δ¹³C mark a zone of maximum organic matter respiration and high nutrient and organic matter availability. The base of this zone at ca 300 m depth corresponds with the transition from massive microbial boundstone to clinostratified grainstone, rudstone and breccia. The microbial boundstone facies apparently formed only in seawater enriched in organic matter, possibly because this organic matter sustained benthic microbial communities at Latemar. The base of slope microbialites on high‐relief microbial carbonate platforms may be a proxy for the depth to maximum respiration zones of Palaeozoic and Mesozoic periplatform basins.     

SIMS Bias on Isotope Ratios in Ca‐Mg‐Fe Carbonates (Part III): δ18O and δ13C Matrix Effects Along the Magnesite–Siderite Solid‐Solution Series

This study explores the effects of cation composition on mass bias (i.e., the matrix effect), which is a major component of instrumental mass fractionation (IMF) in the microanalyses of δ¹³C and δ¹⁸O by SIMS in carbonates of the magnesite–siderite solid‐solution series (MgCO₃–FeCO₃). A suite of twelve calibration reference materials (RMs) was developed and documented (calibrated range: Fe# = 0.002–0.997, where Fe# = molar Fe/[Mg + Fe]), along with empirical expressions for regressing calibration data (affording residuals < 0.5‰ relative to certified reference material NIST‐19). The calibration curves of both isotope systems are non‐linear and have, over a 2‐year period, fallen into one of two distinct but largely self‐consistent shape categories (data from ten measurement sessions), despite adherence to well‐established analytical protocols for carbonate δ¹³C and δ¹⁸O analyses at WiscSIMS (CAMECA IMS 1280). Mass bias was consistently most sensitive to changes in composition near the magnesite end‐member (Fe# 0–0.2), deviating by up to 4.5‰ (δ¹³C) and 14‰ (δ¹⁸O) with increasing Fe content. The cause of variability in calibration curve shapes is not well understood at present and demonstrates the importance of having available a sufficient number of well‐characterised RMs so that potential complexities of curvature can be adequately delineated and accounted for on a session‐by‐session basis.     

连续流同位素质谱测定水中溶解无机碳含量和碳同位素组成的方法研究

用连续流同位素质谱对水样中溶解无机碳含量和碳同位素组成的测量方法进行了研究,使用德国Finnigan公司DeltaPlusXP同位素质谱仪和GasBenchⅡ在线制样装置对实验室制备的四个实验室标准进行了反应流程、平衡时间、信号强度、数据精度、标准稳定性等检测,结果显示平衡时间大于4h检测信号达到稳定,同时发现44CO2信号强度和水样中溶解无机碳(DIC)浓度具有很好的相关性,因此可以利用信号强度来计算原样品中的DIC浓度。在四个实验室标准中,由NaHCO3配置的标准具有非常好的稳定性和精度,可以作为测试的工作标准。本方法测量水样中溶解无机碳的δ13C分析精度为0.1‰。本方法可以广泛应用于自然界各种水体中溶解无机碳(DIC)含量及其稳定碳同位素组成的分析。     

湖南晚二叠世生物礁成岩作用的碳,氧同位素研究

本文通过对湖南晚二叠世生物礁中的有关胶结物及岩石的碳、氧稳定同位素研究,并结合薄片观察、探针成分分析、包裹体测温等,探讨了该地区生物礁成岩作用中的有关成岩特征。研究认为：①湖南晚二叠世生物礁中胶结物从早期到晚期δ＾１３Ｃ和δ＾１８Ｏ值总体上均有变轻的趋势,反映了礁体为一连续埋藏的成岩过程;②生物礁中所见白云石化现象主要属埋藏压实成因,礁休基本未受早期淡水或混合水影响;③礁中粗晶方解石胶结物形成于深     

渤海东海海洋沉积物中碳氮稳定同位素标准物质研制

海洋沉积物中碳氮稳定同位素因其能够确定有机质的来源,有助于了解碳循环、气候变化、有机质迁移转化而备受关注,但其分析测试过程中尚缺乏海洋沉积物碳氮稳定同位素标准物质进行质量监控。本文依据ISO导则35和国家《一级标准物质技术规范》(JJG1006—1994),研制了三个海洋沉积物碳氮稳定同位素标准物质(MSCNI-1、MSCNI-2和MSCNI-3),候选物样品分别采自我国渤海锦州湾湿地、东海闽浙近岸和东海冲绳海槽,定值组分为总碳氮同位素(δ~(13)C-TC、δ~(15)N-TN)和有机碳氮同位素(δ~(13)C-C~(org)、δ~(15)N-N~(org)),定值方法采用元素分析-同位素比值质谱法(EA-IRMS)多家实验室协同定值。经检验,三个标准物质候选物均匀性良好,一年内定值组分均无显著变化,具有良好的稳定性;δ~(13)C和δ~(15)N的标准不确定度分别小于0.15%和0.24%,标准值和标准不确定度合理。该套标准物质是我国以海底沉积物为介质的基体型碳氮稳定同位素标准物质,定值方法准确可靠,可供海洋、地质及环境等相关领域实验室用于仪器校准、方法评价和质量监控等。     

Dissolved carbon in pore waters from the carbonate barrier reef of Tahiti (French Polynesia) and its basalt basement

This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg^–1 pH of 7.6 and p(CO₂) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg^–1, pH of 7.70 and p(CO₂) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO₂) up to 5.6 times the atmospheric P(CO₂).     

Characterization, lateral variability and lateral extent of discontinuity surfaces on a Carbonate Platform (Barremian to Lower Aptian, Oman)

Hiati of various duration in carbonates are commonly expressed as discontinuity surfaces. The understanding of processes that form and affect these surfaces leads to an improved sequence-stratigraphic interpretation, a reliable outcrop correlation, and better models for reservoir compartmentalization. Various intraformational discontinuities were analysed and interpreted in a well-exposed study window, 2·5 km in lateral length and 60 m in height comprising the Barremian-Aptian Qishn Formation (Haushi-Huqf area, central Oman). This study focuses on the lateral extent and morphology of the surfaces, the petrography of the underlying rocks, and the facies changes and geochemical trends across these discontinuities. Furthermore, the lateral variability of discontinuity surfaces was documented. Three genetic types of discontinuities are differentiated: (i) erosion surfaces; (ii) omission surfaces (hard- and firmgrounds); and (iii) composite surfaces with evidence for both subaerial exposure and submarine boring. Field observations, combined with petrographic and geochemical data, suggest that 17 surfaces are laterally extensive for at least 20 km and record relative sea-level fluctuations of regional scale. In contrast, a large number of laterally limited surfaces (<1 km) are related to locally active processes such as waves and current erosion. The lateral variability along extensive surfaces is the result of the depositional environment below the discontinuity, the sea-floor topography, waves and currents and differential erosion. The most pronounced lateral variability is present along six laterally extensive composite surfaces that record terrestrial exposure and subsequent flooding of a tidal flat environment. This variability is caused by spatial variability in the tidal flat environment, meteoric alteration and differential erosion. This study emphasizes the spatial and temporal complexity of processes that form and modify discontinuity surfaces. This variability must be kept in mind when interpretations and correlations are based on one-dimensional sections or cores.     

Global significance of the carbon cycle in the karst dynamic system: evidence from geological and ecological processes

On the basis of proposing the existence of a karst carbon cycle and carbon sink at a watershed scale, this paper provides four pieces of evidence for the integration of geology and ecology during the carbon cycle processes in the karst dynamic system, and estimated the karst carbon sink effect using the methods of comparative monitoring of paired watersheds and the carbon stable isotope tracer technique. The results of the soil carbon cycle in Maocun, Guilin, showed that the soil carbon cycle in the karst area, the weathering and dissolution of carbonate rocks under the soil, resulted in a lower soil respiration of 25% in the karst area than in a non-karst area (sandstone and shale), and the carbon isotope results indicated that 13.46% of the heavy carbon of the limestone is involved in the soil carbon cycle. The comparative monitoring results in paired watersheds, suggesting that the HCO₃^- concentration in a karst spring is 10 times that of a rivulet in a non-karst area, while the concentration of inorganic carbon flux is 23.8 times. With both chemical stoichiometry and carbon stable isotopes, the proportion of carbon in karst springs derived from carbonate rocks was found to be 58.52% and 37.65% respectively. The comparison on carbon exchange and isotopes at the water-gas interface between the granite and carbonate rock basins in the Li River showed that the CO₂ emission of the karst water is 10.92 times that of the allogenic water from the non-karst area, while the carbon isotope of HCO₃^- in karst water is lighter by 8.62‰. However, this does not mean that the karst water body has a larger carbon source effect. On the contrary, it means the karst water body has a greater karst carbon sink effect. When the karst subterranean stream in Zhaidi, Guilin, is exposed at the surface, carbon-rich karst water stimulated the growth of aquatic plants. The values of carbon stable isotopes in the same species of submerged plants gradually becomes heavier and heavier, and the 512 m flow process has a maximum range of 15.46‰. The calculation results showed that 12.52% of inorganic carbon is converted into organic carbon. According to the data that has been published, the global karst carbon sink flux was estimated to be 0.53-0.58 PgC/a, equivalent to 31.18%-34.41% of the global forest carbon sink flux. In the meanwhile, the karst carbon sink flux in China was calculated to be 0.051 PgC/a, accounting for 68% of its forest carbon sink flux.     

Paragenesis of Cretaceous to Eocene carbonate reservoirs in the Ionian fold and thrust belt (Albania): relation between tectonism and fluid flow

ABSTRACT This paper examines the diagenetic history of dual (i.e. matrix and fracture) porosity reservoir lithologies in Cretaceous to Eocene carbonate turbidites of the Ionian fold and thrust belt, close to the oil‐producing centre of Fier–Ballsh (central Albania). The first major diagenetic event controlling reservoir quality was early cementation by isopachous and syntaxial low‐Mg calcite. These cements formed primarily around crinoid and rudist fragments, which acted as nucleation sites. In sediments in which these bioclasts are the major rock constituent, this cement can make up 30% of the rock volume, resulting in low effective porosity. In strata in which these bioclasts are mixed with reworkedmicrite, isopachous/syntaxial cements stabilized the framework, and matrixporosity is around 15%. The volumetric importance of these cements, their optical and luminescence character (distribution and dull orange luminescence) and stable isotopic signal (δ¹⁸O and δ¹³C averaging respectively; ?0·5‰ VPDB and +2‰ VPDB) all support a marine phreatic origin. Within these turbidites and debris flows, several generations of fractures alternated with episodes of cementation. A detailed reconstruction of this history was based on cross‐cutting relationships of fractures and compactional and layer‐parallel shortening (LPS) stylolites. The prefolding calcite veins possess orange cathodoluminescence similar to that of the host rock. Their stable isotope signatures (δ¹⁸O of ?3·86 to ?0·85‰ VPDB and δ¹³C of – 0·14 to + 2·98‰ VPDB) support a closed diagenetic rock‐buffered system. A similar closed system accounts for the selectively reopened and subsequently calcite‐cemented LPS stylolites (δ¹⁸O of ?1·81 to ?1·14‰ VPDB and δ¹³C of +1·52 to +2·56‰ VPDB). Within the prefolding veins, brecciated host rock fragments and complex textures such as crack and seal features resulted from hydraulic fracturing. They reflect expulsion of overpressured fluids within the footwall of the frontal thrusts. After folding and thrust sheet emplacement, some calcite veins are still rock buffered (δ¹⁸O of ?0·96 to +0·2‰ VPDB and δ¹³C of +0·79 to +1·37‰ VPDB), whereas others reflect external (i.e. extraformational) and thus large‐scale fluid fluxes. Some of these veins are linked to basement‐derived fluid circulation or originated from fluid flow along evaporitic décollement horizons (δ¹⁸O around +3·0‰ VPDB and δ¹³C around +1·5‰ VPDB). Others are related to the maturation of hydrocarbons in the system (δ¹⁸O around ?7·1‰ VPDB and δ¹³C around +9·3‰ VPDB). An open joint system reflecting an extensional stress regime developed during or after the final folding stage. This joint system enhanced vertical connectivity. This open joint network can be explained by the high palaeotopographical position and the folding of the reservoir analogue within the deformational front. The joint system is pre‐Burdigalian in age based upon a dated karstified discordance contact. Sediment‐filled karst cavity development is linked to meteoric water infiltration during emergence of some of the structures. Despite its sediment fill, the karst network is locally an important contributor to reservoir matrix porosity in otherwise tight lithologies. Development of secondary porosity along bed‐parallel and bed‐perpendicular (i.e. layer‐parallel shortening) stylolites is interpreted as a late‐stage diagenetic event associated with migration of acidic fluids during hydrocarbon maturation. Development of porosity along the LPS system enhanced the vertical reservoir connectivity.     

Aragonite stromatolitic buildups from Santorini (Aegean Sea,Greece): Geochemical and palaeontological constraints of the caldera palaeoenvironment prior to the Minoan eruption (ca 3600 yr bp)

The pyroclastic deposits of the Minoan eruption (ca 3600 yr bp ) in Santorini contain abundant xenoliths. Most of these deposits are calcareous blocks of laminated‐botryoidal, stromatolite‐like buildups that formed in the shallow waters of the flooded pre‐Minoan caldera; they consist of (i) light laminae, of fibrous aragonite arranged perpendicular to layering, and (ii) dark laminae, with calcified filaments of probable biological origin. These microstructures are absent in the light laminae, suggesting a predominant inorganic precipitation of aragonite on substrates probably colonized by microbes. Internal cavities contain loose skeletal grains (molluscs, ostracods, foraminifera and diatoms) that comprise taxa typical of shallow marine and/or lagoon environments. Most of these forms are typical of warm water environments, although no typical taxa from hydrothermal vents have been observed. Past gasohydrothermal venting is recorded by the occurrence of barite, pyrolusite and pyrite traces. The most striking features of the stable isotopic data set are: (i) an overall wide range in δ¹³C_PDB (0·16 to 12·97‰) with a narrower variation for δ¹⁸O_PDB (?0·23 to 4·33‰); and (ii) a relatively uniform isotopic composition for the fibrous aragonite (δ¹³C = 12·40 ± 0·43‰ and δ¹⁸O = 2·42 ± 0·77‰, n = 21). The δ¹³C and δ¹⁸O values from molluscs and ostracods display a covariant trend, which reflects a mixing between sea water and a fluid influenced by volcano‐hydrothermal activity. Accordingly, ⁸⁷Sr/⁸⁶Sr from the studied carbonates (0·708758 to 0·709011 in fibrous aragonite and 0·708920 to 0·708991 in molluscs) suggests that the aragonite buildups developed in sea water under the influence of a hydrothermal/volcanic source. Significant differences in trace elements have been detected between the fibrous aragonite and modern marine aragonite cements. The caldera water from which the fibrous aragonite crusts formed received an input from a volcano‐hydrothermal system, probably producing diffuse venting of volcanogenic CO₂ gas and of a fluid enriched in Ca, Mn and Ba, and depleted in Mg and probably in Sr.     

典型黄土塬区地下水水化学成因机制及碳循环意义

水岩相互作用包括了溶解、沉淀和离子交换等作用, 其参与了各种地质作用和生态-环境过程; 而目前对离子交换作用在水中离子来源解析和同位素示踪等方面考虑不足, 这限制了对水化学演化规律和碳循环刻画等方面的认识。本研究选择水文地质条件较为简单的甘肃陇东地区董志塬, 在对降水入渗补给评估、地下水定年(³H和¹⁴C)等水循环规律刻画的基础上, 通过对降水元素输入和阳离子交换容量分析, 以及应用硝酸盐同位素(δ¹⁵N-NO₃和δ¹⁸O-NO₃)、硫酸盐同位素(δ³⁴S-SO₄和δ¹⁸O-SO₄)、⁸⁷Sr/⁸⁶Sr (包括地下水及黄土各分量)、阳离子关系等手段, 解析了董志塬地下水中主要离子来源。研究结果显示, 降水入渗补给量为39±8mm/a, 土壤水运移速度为0.13±0.03m/a; 研究区包气带较厚(主要在40~75m), 这说明年降水需要250~750年才能补给到地下水, 但持续的补给使得自然条件下每年约有(3167±650)×10⁴m³地下水通过泉水补给两侧河流。地下水年龄较老, 不含³H, ¹⁴C校正年龄在417年至19420年之间, 因此水化学组成受现代人类活动影响可忽略; 地下水中Cl^-和SO₄^2-主要来自于古降水, 并反演出古降水SO₄^2-平均含量为1.2mg/L, 显著低于受化石燃料等影响的现代含量(平均为6.6mg/L); 而地下水NO₃^-则主要来自于土壤氮的硝化。地下水⁸⁷Sr/⁸⁶Sr比值(0.7107至0.7114)与黄土中碳酸盐的比值(0.7103至0.7111)基本一致, 表明Ca²⁺和Mg²⁺主要来自于碳酸盐矿物的溶解, 部分被吸附至粘土矿物。研究区黄土具有较高的阳离子交换容量(149±33meq/kg), 地下水总Na⁺中, 降水贡献平均占29%, 其余Na⁺主要来源于水中Ca²⁺和Mg²⁺和粘土矿物中Na的交换(平均为71%), 硅酸盐溶解对水中Na⁺贡献可忽略(硅酸盐溶解会导致⁸⁷Sr/⁸⁶Sr增加), 而以往研究大多认为除了降水输入、蒸发岩溶解外, 水中Na⁺主要来自于硅酸盐矿物的溶解, 并贡献了碳汇。本研究认为在研究区地下水中, 硅酸盐风化的碳汇效应可忽略; 同时强调了在含有粘土矿物的流域或水岩体系, 阳离子交换作用在示踪水中离子来源及碳循环中的重要性。

     

Multi‐proxy constraints on the significance of covariant δ13C values in carbonate and organic carbon during the early Mississippian

This study investigates the covariation between carbonate and organic δ¹³C values in a proximal to distal transect of four outcrops in the Madison Limestone in the Western United States Rockies, combined with δ³⁴S values of carbonate associated sulphate, the concentration of acid‐insoluble material and measurements of total organic carbon. These new geochemical datasets not only allow for an evaluation of carbon isotope covariance during one of the largest perturbations to the global carbon cycle over the past 550 Myr, but also constrain the cause of the excursion in carbonate δ¹³C values. The results support the hypothesis that a period of anoxia did not play a role in generating the positive carbonate δ¹³C values, but rather favour interpretations by previous workers that the proliferation of land plants destabilized the Carboniferous carbon cycle, setting the stage for a significant change in the carbonate δ¹³C values of contemporaneous marine carbonates. These results also demonstrate that one of the largest perturbations to the global carbon cycle did not produce synchronous variations in carbonate and organic δ¹³C values, emphasizing the importance of local depositional controls on carbon isotope covariance in the geological record in both modern and ancient environments.     

Dinosaur coprolites from the Late Cretaceous (Maastrichtian) Lameta Formation of India: isotopic and other markers suggesting a C3plant diet

A single locality of the Late Cretaceous (Maastrichtian) Lameta Formation at Pisdura in Central India has yielded a large number of coprolites attributed to titanosaurian dinosaurs. Internally the coprolites are dark grey and contain abundant plant tissues and other organic materials. The plant tissues are mostly of gymnospermous origin. In addition, remains of bacterial colonies, fungal spores and algae are seen in the macerated fraction under scanning electron microscope. The dark grey appearance is probably attributable to fine-grained organic matter within voids in tracheids or xylem. The average ¹³C/¹²C ratio of the organic matter in the coprolites is -24‰ (relative to PDB) suggesting that plants of C₃type were the main diet of their producers. A comparison of δ¹⁵N value (about 4‰ w.r.t. air) of the coprolites with that of faecal matter of modern herbivores and carnivores suggests that gut fermentation may not have been an active mechanism in the digestion process of titanosaurs.     

Petrography and geochemistry of septarian carbonate concretions from the Boom Clay Formation (Oligocene,Belgium)

The septarian carbonate concretions from the Boom Clay (Belgium) consist mainly of authigenic minerals such as micrite ( 70% bulk volume) and pyrite framboids ( 3%). These mineral phases occur between detrital grains and fossils. The septarian cracks are lined with calcite, which is sometimes covered with pyrite. The preservation of delicate sedimentological features in the concretion matrix (hardly compacted faecal pellets, burrows and uncrushed shells) points to an early origin of the concretions. Systematic geochemical variations from concretion centre to edge suggest that growth continued during shallow burial. The13C values (–17.5 to –20.5) of the concretionary carbonate show that bacterial sulphate-reduction processes were dominant. Sulphate-reduction-derived HCO3- was diluted by marine-related HCO3-, derived from dissolved bioclasts. A slight enrichment in 13C during growth is caused by the decreasing influence of sulphate reduction because of the progressive closure of the diagenetic system due to shallow-burial compaction. The 18O values (–0.5 to +1.0) of the concretionary carbonate point to a marine origin. The slightly 18O-depleted signature with respect to time-equivalent marine-derived carbonate relates to the incorporation of an 18O-depleted component, originating from sulphate and organic matter. The slight decrease in 18O during growth relates to an increasing influence of this component and to a decreasing influence of seawater-derived oxygen during early diagenesis.     

Middle pleistocene variations in palaeoclimate,palaeoenvironment and vegetation of the las tablas de daimiel national park (Spain)

The Middle Pleistocene palaeoclimate and palaeoenvironment evolution of the Las Tablas de Daimiel wetlands is described using a combination of sedimentology, pollen and δ¹³C and δ¹⁸O isotopic records of Unit B of core LT‐199906. This unit mostly contains fluvial and palustrine sediments. U/Th and amino acid racemization (AAR) dating and a comparison of the δ¹⁸O curve of Unit B with oceanic records suggests that Unit B spans the period from the end of Marine Isotope Stage (MIS) 10 (340 ka) to the first stages of MIS 7 (ca. 210 ka). MIS 9 was characterised by a regional vegetation dominated by Cupressaceae, with Pinus as a tree element. The water level was high and temperatures were very probably higher than during the Holocene. MIS 8 and the first substages of MIS 7 (7e, 7d and 7c) were dominated by xerophilous steppe vegetation in lowlands (elevations around 610 m above sea level) near to the wetland. At higher altitudes, far away from the wetland, there were fewer Pinus than in MIS 9, and a greater presence of warm, temperate and cool climate tree elements. The aquatic system in MIS 9 became shallower, with eutrophication and the accumulation of organic matter occurring; temperatures were similar to or lower than those of the Holocene. Copyright © 2011 John Wiley & Sons, Ltd.     

Holocene climate reconstructions of Ulungur Lake (Xinjiang,China) inferred from ostracod species assemblages and stable isotopes

In this paper, the data on the paleoclimatic and paleoenvironmental changes during the Holocene are presented and a discussion is made on a 225-cm-long sediment core from Ulungur Lake, located in Northwest China. The chronology is constructed from six AMS radiocarbon dates on the bulk organic matter. On the basis of the analysis of ostracod assemblages and the shell stable isotopes, the core is divided into three paleoclimatic and paleoenvironmental evolution stages: 9 985–5 250 cal.aB.P. stage is the wettest phase of the core section. The climate changed from moderate-dry to cool-wet, and then to warm-wet in turn, and the lake level rose accordingly, showing the characteristic of a high lake level. 5 250–1 255 cal.aB.P. stage was the driest phase of the core sediment. The climate turned from the early warm-dry to the late warm-wet and the lake level fell and rose again. Finally, the 1 255 cal.aB.P. stage was the medium stage of the section. The temperature was low and then increased after the 1920s and the climate was dry. The whole climatic and environmental evolution records of Lake Ulungur were not only in agreement with the sporopollen record of the same core but also in agreement with the record of environmental changes of adjacent areas. It responded to regional environmental changes and global abrupt climate events, following the westerly climate change mode on 100-year-scale, primarily with cold-wet and warmdry characteristics. __________ Translated from Quaternary Sciences, 2007, 27(3):382–391 [译自:第四纪研究]     

中侏罗世泥炭地净初级生产力及其对全球碳循环的响应——以吐哈盆地沙尔湖煤田为例

泥炭地具有明显的碳汇能力, 对减缓全球气候变化有着至关重要的作用, 煤作为泥炭地的最终产物, 保存有丰富的泥炭地发育时期的古环境信息, 成煤泥炭地碳聚集速率和净初级生产力(NPP)可以作为恢复古气候的替代指标。吐哈盆地南缘沙尔湖煤田ZK9E02钻孔中侏罗统西山窑组发育视厚度为121.97 m的煤层(C8), 本研究使用频谱分析对其进行米兰科维奇轨道周期的识别及成煤泥炭地发育时限的估算, 然后利用该时限, 结合煤的碳含量以及煤化作用阶段的碳损, 计算出成煤泥炭地的NPP, 进而探究成煤泥炭地的碳汇能力与碳循环关系。研究发现, 所研究煤层的自然伽马测井曲线中蕴含着约405 ka长偏心率、约95 ka短偏心率、约37.6 ka斜率、约18.2 ka岁差的米兰科维奇旋回天文周期, 计算出该成煤泥炭地发育的煤层沉积约2218.54~2347.03 ka。该煤层碳含量74.54%, 考虑到煤化过程中的碳损失约为26.75%, 恢复出成煤期泥炭地碳聚集速率为66.11~69.86 g C/m2·a, NPP为265.2~280.2 g C/m2·a。控制泥炭地NPP的主要因素有CO2含量、古纬度、古大气温度等, 研究区较低的泥炭地NPP水平与当时CO2含量过低或古纬度较低有一定关系。泥炭地NPP在一定程度上反映着大气中CO2的变化, 进一步用来揭示全球碳循环对气候变化的动态响应过程, 这对"深时"高分辨率的古环境研究有重要意义。因此, 预测泥炭地NPP的水平, 研究生态系统中碳元素的最终去向, 亦有利于更好地认识到全球碳循环过程中泥炭地的"碳汇"角色, 助力实现"碳达峰、碳中和"目标。     

鄂尔多斯奥陶系碳酸盐岩碳氧同位素特征及其意义*

鄂尔多斯古生代海相地层沉积厚度巨大。鄂尔多斯奥陶系碳酸盐岩的碳氧同位素组成受后期成岩作用影响较小,基本保留了原始海洋的同位素组成： δ¹³C值分布于-7.30‰～2.26‰之间,均值-0.30‰;δ¹⁸O值分布于-13.14‰～-1.94‰之间,均值-6.38‰,碳氧同位素组成与全球基本一致。区域上,鄂尔多斯西缘具有相对较高的δ¹³C值,南缘次之,而东缘最低。纵向上,碳同位素组成逐渐增重,并在中晚奥陶世发生明显的正向偏移,δ¹³C均值由马家沟组的-0.36‰增加到平凉组的0.15‰,至背锅山组增加至0.68‰。碳同位素的区域分布差异表明鄂尔多斯西缘水体相对较深,南缘次之,东缘相对较浅,由早奥陶世至晚奥陶世水体逐渐加深,碳同位素组成反映的海平面变化趋势与沉积相演化一致。鄂尔多斯西南缘中晚奥陶世碳同位素组成的正向偏移,标志着较高的生产力和有机碳埋藏率,具有重要的石油地质学意义,西南缘的平凉组/乌拉力克组和背锅山组是下古生界最重要和有效的烃源岩层。