Pedogenic-phreatic carbonates on a Middle Devonian (Givetian) terrigenous alluvial-deltaic plain, Gilwood Member (Watt Mountain Formation), northcentral Alberta, Canada

In the Muskeg Trough of northcentral Alberta the Gilwood Member contains widespread carbonate deposits that formed within terrigenous mudstone and sandstone hosts. Stratigraphic, depositional and petrographic relationships indicate that these carbonates represent calcretes and dolocretes. Calcretes, observed best with cathodoluminescence, display microcrystalline alpha fabrics, circumgranular cracks, root networks, displacive growth fabrics, elongate channel voids and rare coloform growths with flower spar. Similarly, dolocretes have microcrystalline alpha fabrics, brecciation, gradational contacts with host mudstones, extensive layered nodular horizons and are associated with anhydrite and pyrite. δ¹³C values range between ?7‰ to +1‰ and –6‰ to +3‰ for calcretes and dolocretes, respectively. Oxygen isotopes are more variable and differ with host lithologies. δ¹⁸O of calcretes ranges between ?11‰ to ?8‰ for sandstones and ?8‰ to ?3‰ for mudstones, whereas δ¹⁸O of dolocretes ranges between ?3‰ to 1‰ for marine mudstones and ?6‰ to ?2‰ for pedogenic mudstones. Regional mapping indicates that calcretes thicken towards the deepest parts of the Muskeg Trough. Widespread dolocretes extend beyond the eastern and western limits of Muskeg Trough and are useful marker intervals for regional correlations. Dolocretes of restricted lateral extent are found within gleyed palaeosol mudstones next to calcretized channel sandstones. Calcrete isotopic values are interpreted as indicative of carbonate precipitation from waters with meteoric water input. However, the higher δ¹⁸O values in dolocretes are indicative of a contribution from an isotopically heavier source such as seawater. Stratigraphically, calcretes are most common along the western and northern edges of Muskeg Trough; thus, calcrete accumulation was further controlled by meteoric water in-flow from the highland to the west and sluggish groundwater flow in Muskeg Trough. In contrast, regionally widespread dolocrete horizons appear to have formed from mixing of fresh waters derived from the highland to the west and seawaters introduced from the east. Regionally restricted dolocretes which are found next to channel sandstones formed from groundwater out-flow from the permeable channel sandstones which resulted in calcretization in channel proximal mudstones and dolomitization in channel distal mudstones.     

Early Mississippian sandy siltstones preserve rare vertebrate fossils in seasonal flooding episodes

Flood‐generated sandy siltstones are under‐recognised deposits that preserve key vertebrate (actinopterygians, rhizodonts, and rarer lungfish, chondrichthyans and tetrapods), invertebrate and plant fossils. Recorded for the first time from the lower Mississippian Ballagan Formation of Scotland, more than 140 beds occur throughout a 490 m thick core succession characterised by fluvial sandstones, palaeosols, siltstones, dolostone ‘cementstones’ and gypsum from a coastal–alluvial plain setting. Sandy siltstones are described as a unique taphofacies of the Ballagan Formation (Scotland, UK); they are matrix‐supported siltstones with millimetre‐sized siltstone and very fine sandstone lithic clasts. Common bioclasts include plants and megaspores, fish, ostracods, eurypterids and bivalves. Fossils have a high degree of articulation compared with those found in other fossil‐bearing deposits, such as conglomerate lags at the base of fluvial channel sandstones. Bed thickness and distribution varies throughout the formation, with no stratigraphic trend. The matrix sediment and clasts are sourced from the reworking of floodplain sediments including desiccated surfaces and palaeosols. Secondary pedogenic modification affects 30% of the sandy siltstone beds and most (71%) overlie palaeosols or desiccation cracks. Sandy siltstones are interpreted as cohesive debris flow deposits that originated by the overbank flooding of rivers and due to localised floodplain sediment transport at times of high rainfall; their association with palaeosols and desiccation cracks indicates seasonally wet to dry cycles throughout the Tournaisian. Tetrapod and fish fossils derived from floodplain lakes and land surfaces are concentrated by local erosion and reworking, and are preserved by deposition into temporary lakes on the floodplain; their distribution indicates a local origin, with sediment transported across the floodplain in seasonal rainfall episodes. These deposits are significant new sites that can be explored for the preservation of rare non‐marine fossil material and provide unique insights into the evolution of early terrestrial ecosystems.     

Growth mechanisms and geochemistry of carbonate concretions from the Cambrian Wheeler Formation (Utah,USA)

Carbonate concretions provide unique records of ancient biogeochemical processes in marine sediments. Typically, they form in organic‐rich mudstones, where a significant fraction of the bicarbonate required for carbonate precipitation is supplied from the decomposition of organic matter in the sediments. As a result, carbonates that comprise concretions are usually characterized by broad ranges in δ¹³C and include values that are significantly depleted relative to seawater. This article reports results from a physical, petrographic and geochemical analysis of 238 concretions from the Wheeler Formation (Cambrian Series 3), Utah, USA, which are unusual in several respects. Most prominently, they formed in organic‐poor mudstones (total organic carbon = 0·1 to 0·5%) and are characterized by a narrow range of δ¹³C that onlaps the range of contemporaneous seawater values. Subtle centre to edge trends in δ¹³C demonstrate that concretion precipitation was initiated by local chemical gradients set up by microbial activity in the sediments, but was sustained during growth by a large pool of inorganic bicarbonate probably derived from alkaline bottom waters. The large inorganic pool appears to have been important in facilitating rapid precipitation of the concretion matrix, which occurred via both displacive and replacive carbonate precipitation during early diagenesis. Stable isotope data from cogenetic pyrite (δ³⁴S) and silica (δ¹⁸O) phases provide insight into the evolution of biogeochemical processes during concretion growth, and suggest that concretions were formed almost entirely during sulphate reduction, with only minor modification thereafter. Concretions of the Wheeler Formation appear to represent an end‐member system of concretion formation in which rapid growth was promoted by ions supplied from sea‐water. As such, they offer insight into the spectrum of processes that may influence the growth of carbonate concretions in marine sediments.     

Dinosterol δD values in stratified tropical lakes (Cameroon) are affected by eutrophication

In freshwater settings, dinosterol (4α,23,24-trimethyl-5α-cholest-22E-en-3β-ol) is produced primarily by dinoflagellates, which encompass various species including autotrophs, mixotrophs and heterotrophs. Due to its source specificity and occurrence in lake and marine sediments, its presence and hydrogen isotopic composition (δD) should be valuable proxies for paleohydrological reconstruction. However, because the purity required for hydrogen isotope measurements is difficult to achieve using standard wet chemical purification methods, their potential as a paleohydrological proxy is rarely exploited. In this study, we tested δD values of dinosterol in both particulate organic matter (POM) and sediments of stratified tropical freshwater lakes (from Cameroon) as a paleohydrological proxy, the lakes being characterized by variable degrees of eutrophication. In POM and sediment samples, the δD values of dinosterol correlated with lake water δD values, confirming a first order influence of source water δD values. However, we observed that sedimentary dinosterol was D enriched from ca. 19 to 54‰ compared with POM dinosterol. The enrichment correlated with lake water column conditions, mainly the redox potential at the oxic–anoxic interface (E_h OAI). The observations suggest that paleohydrologic reconstruction from δD values of dinosterol in the sediments of stratified tropical lakes ought to be sensitive to the depositional environment, in addition to lake water δD values, with more positive dinosterol δD values potentially reflecting increasing lake eutrophication. Furthermore, in lake sediments, the concentration of partially reduced vs. non-reduced C₃₄ botryococcenes, stanols vs. stenols, and bacterial (diploptene, diplopterol and ββ-bishomohopanol) vs. planktonic/terrestrial lipids (cholesterol, campesterol and dinosterol) correlated with E_h OAI. We suggest using such molecular proxies for lake redox conditions in combination with dinosterol δD values to evaluate the effect of lake trophic status on sedimentary dinosterol δD values, as a basis for accurately reconstructing tropical lake water δD values.     

Carbon,oxygen and sulphur isotope variations in concretions from the Upper Lias of N.E. England

Carbon, oxygen and sulphur isotope data for transects across two pyrite-bearmg carbonate concretions, and their host sediments, from the Upper Lias of N.E. England show symmetrical zonation. δ¹³C_PDB values of the calcite cement (?12.9 to ?15.4%.) indicate that most of it originated from organic matter by bacterial reduction of sulphate, augmented with marine and, to a lesser extent, fermentation derived carbonate. Organic carbon (δ¹³C_PDB = ?26.1 to ?37.0%.). reflects the admixture of allochtho-nous terrestrial organic matter with marine material and the selective preservation of isotopically light organic material through microbiological degradation.Two phases of pyrite are present in each concretion. The earlier framboidal pyrite formed throughout the sediment prior to concretionary growth and has δ³⁴S_CD values of ?22 to ?26%. indicating formation by open system sulphate reduction. The later euhedral phase is more abundant and reaches values of ? 2.5 to ? 5.5%. at concretion margins. This phase of sulphate reduction provided the carbonate source for concretionary growth and occurred in a partially closed system. The δ¹³C and δ³⁴S data are consistent with mineralogical and chemical evidence which suggest that both concretions formed close to the sediment surface. The δ₁₈O values of the calcite in one concretion (δ¹⁸O_PDB = 2.3 to ?4.8%.) indicate precipitation in pore waters whose temperature and isotopic composition was close to that of overlying seawater. The other concretion is isotopically much lighter (δ¹⁸O_PDB?8.9 to ?9.9%.) and large δ¹⁸O differences between concretions in closely-spaced horizons imply that local factors control the isotopic composition of pore waters.     

Pore water evolution in sandstones of the Groundhog Coalfield,northern Bowser Basin,British Columbia

The succession of sandstone cements in chert and volcanic lithic arenites and wackes from the northern Bowser Basin of British Columbia comprises a record of diagenesis in shallow marine, deltaic, and coastal plain siliciclastic sediments that pass through the oil window and reach temperatures near the onset of metamorphism. The succession of cements is consistent with seawater in the sandstones mixing with acid waters derived from dewatering of interbedded organic rich muds. Sandstone cement paragenesis includes seven discrete cement stages. From earliest to latest the cement stages are: (1) pore-lining chlorite; (2) pore-lining to pore-filling illite; (3) pore-filling kaolinite; (4) oil migration through some of the remaining connected pores; (5) chlorite dissolution; (6) quartz cement; and (7) calcite cement. These seven cement stages are interpreted as a record of the evolution of pore waters circulating through the sandstones after burial. The earliest cement stages, as well as the depositional environments, are compatible with seawater as the initial pore fluid. Seawater composition changed during transport through the sandstones, first by loss of Mg²⁺ and Fe²⁺ during chlorite precipitation (stage 1). Dewatering of interbedded organic-rich mudstones probably added Mg²⁺ and Fe²⁺ to partially buffer the loss of these cations to chlorite. Acids produced during breakdown of organic matter are presumed to have mixed into sandstone pore fluids due to further compaction of the muds, leading to reduction of initial alkalinity. Reduction in alkalinity, in turn, favours change from chlorite to illite precipitation (stage 2), and finally to kaolinite (stage 3). Pore waters likely reached their peak acidity at the time of oil migration (stage 4). Chlorite dissolution (stage 5) and quartz precipitation (stage 6) occurred when pores were filled by these hydrocarbon-bearing and presumably acidic fluids. Fluid inclusions in fracture-filling quartz cements contain petroleum, high-pressure methane, and methane-rich aqueous solutions. Homogenization temperatures from primary two-phase inclusions are consistent with quartz cementation during progressive heating between approximately 100 and 200°C. Following quartz precipitation, alkaline pore waters were re-established, as evidenced by late-stage calcite cement (stage 7).     

Early diagenetic siderite as an indicator of depositional environment in the Triassic Rewan Group, southern Bowen Basin, eastern Australia

Early concretionary and non-concretionary siderites are common in subsurface Triassic sandstones and mudrocks of the Rewan Group, southern Bowen Basin. A detailed petrological and stable isotopic study was carried out on these siderites in order to provide information on the depositional environment of the host rocks. The siderites are extremely pure, containing 85–97 mol% FeCO₃, and are commonly enriched in manganese. δ¹³C (PDB) values are highly variable, ranging from - 18·4 to +2·9‰, whereas δ¹⁸O (PDB) values are very consistent, ranging from - 14·0 to - 10·2‰ (mean= - 11·9 ± 1·0‰). The elemental and oxygen isotopic composition of the siderites indicates that only meteoric porewaters were involved in siderite formation, implying that host rocks accumulated in totally non-marine environments. The carbon isotopic composition of the siderites is interpreted to reflect mixing of bicarbonate/carbon dioxide generated by methane oxidation and methanogenesis. Very low δ¹³C values demonstrate that, contrary to current views, highly ¹³C-depleted siderite can be produced at shallow burial depths in anoxic non-marine sediments.     

Onshore climate change during the Late Triassic marine inundation of the Central European Basin

Sedimentological, pedological and palynological evidence reveal radically increasing onshore humidity during the Rhaetian marine invasion of central Europe along the north-eastern margin of the Central European Basin (southern Sweden). Pre-Rhaetian aridity favoured the formation of Carnian redbeds with calcrete, which were succeeded by Norian hematite-cemented conglomerates, arkoses, arkosic wackestones, and smectititic mudstones deposited on braidplains and in lakes. Superimposed autochthonous coals and gleysols indicate the Rhaetian onset of year-round humidity. Chemically mature sandstones, kaolinitic mudstones and luvisols also formed at this time, influenced by a permanent vegetation cover which lowered soil pH and strongly intensified chemical weathering. The Rhaetian deposits accumulated in floodplain lakes repeatedly subjected to sediment infill, plant colonization and palaeosol development. The humidity shift resembles that contemporaneously recorded in the North Sea region.     

The enigma of fine-grained alluvial basin fills: the Permo-Triassic (Cumbrian Coastal and Sherwood Sandstone Groups) of the Solway Basin,NW England and SW Scotland)

The late Permian to Triassic sediments of the Solway Basin consist of a layer-cake succession of mature, predominantly fine-grained red clastics laid down in semi-arid alluvial plain to arid sabkha and saline marginal marine or lacustrine environments. The Cumbrian Coastal Group consists of Basal Clastics and Eden Shales. The Basal Clastics are thin regolith deposits resting unconformably on all-underlying units and are composed of mixtures of angular local gravel and far-transported fine to very fine-grained sands deposited as basal lag. The Eden Shales are predominantly gypsiferous red silty mudstones, with thin very fine-grained sandstone beds, and with thick marine gypsum beds at the base, deposited at a saline lake margin. The overlying Triassic Sherwood Sandstone Group consists of the Annan and Kirklinton Sandstones. The Annan Sandstones are predominantly thick-bedded, multi-storied, fine-grained mature red quartz sandstones in which coarse sand is practically absent despite channels with clay pebbles up to 30 cm in diameter. The overlying, predominantly aeolian, Kirklinton Sandstones consist of festoon cross-bedded and parallel-laminated fine-grained sandstones, almost identical to the Annan Sandstones except that mica and clay are absent. The Stanwix Shales, located above, consist of interbedded red, blue and green mudstones, siltstones, and thin very fine-grained sandstones, with gypsum layers. Although the entire succession can plausibly be interpreted as deposited in a large desert basin opening into a hypersaline marine or lacustrine embayment to the southwest, the uniformly fine-grained nature of the succession is unusual, as is the absence of paleosols, and body and trace fossils. There is almost no coarse sand even in the river channel units, and it seems likely that the basin was not only extremely arid but supplied predominantly by wind rather than water.     

Carbon and Oxygen Isotopic Compositions: How Lacustrine Environmental Factors Respond in Northwestern and Northeastern China

Surface lake sediments,28 from Hoh Xil,24 from northeastern China,99 from Lake Bosten,31 from Ulungur and 26 from Heihai were collected to determine δ13C and δ18O values.Considering the impact factors,conductivity,alkalinity,pH,TOC,C/N and carbonate-content in the sediments,Cl,P,S,and metal element ratios of Mg/Ca,Sr/Ca,Fe/Mn of bulk sediments as environmental variables enable evaluation of their influences on δ13C and δ18O using principal component analysis(PCA) method.The closure and residence time of lakes can influence the correlation between δ13C and δ18O.Lake water will change from fresh to brackish with increasing reduction and eutrophication effects.Mg/Ca in the bulk sediment indicates the characteristic of residence time,Sr/Ca and Fe/Mn infer the salinity of lakes.Carbonate formation processes and types can influence the δ13C–δ18O correlation.δ18O will be heavier from Mg-calcite and aragonite formed in a high-salinity water body than calcite formed in freshwater conditions.When carbonate content is less than 30%,there is no relationship with either δ13C or δ18O,and also none between δ13C and δ18O.More than 30%,carbonate content,however,co-varies highly to δ13C and δ18O,and there is also a high correlation between δ13C and δ18O.Vegetation conditions and primary productivity of lakes can influence the characteristics of δ13C and δ18O,and their co-variance.Total organic matter content(TOC) in the sediments is higher with more terrestrial and submerged plants infilling.In northeastern and northwestern China,when organic matter in the lake sediments comes from endogenous floating organisms and algae,the δ13C value is high.δ13C is in the range of 4‰ to 0‰ when organic matter comes mainly from floating organisms(C/N<6);in the range of 4‰ to 8‰ when organic matter comes from diatoms(C/N=6 to 8);and 8‰ to 4‰ when organic matter comes from aquatic and terrestrial plants(C/N>8).     

Distinction between the Storegga tsunami and the holocene marine transgression in coastal basin deposits of western Norway

Many coastal lakes were inundated by both the Storegga tsunami (7000 ¹⁴C yr BP) and the mid-Holocene sea-level rise (the Tapes transgression) in western Norway. The tsunami eroded lake bottoms and deposited graded and/or massive beds of sand, rip-up clasts, and coarse plant material. By contrast, when the rising sea entered the lakes, it deposited only gyttja, silt and fine sand, without causing much erosion of the underlying lake sediments. Storegga tsunami deposits in some coastal lakes were interpreted previously as ordinary marine sediments from the Tapes transgression. Our reinterpretation of these deposits shows that the transgression maximum phase was reached after 6500 yr BP, more than 1000 yr later than previously inferred for the coast of Sunnmøre. The new data cannot be combined in a shoreline diagram without showing the 6000 yr BP and 7000 yr BP shorelines as slightly warped. © 1998 John Wiley & Sons, Ltd.     

Origin of quartz geodes from Laño and Tubilla del Agua sections (middle–upper Campanian,Basque‐Cantabrian Basin,northern Spain): isotopic differences during diagenetic processes

Quartz geodes and nodular chert have been found within middle–upper Campanian carbonate sediments from the Laño and Tubilla del Agua sections of the Basque‐Cantabrian Basin, northern Spain. The morphology of geodes together with the presence of anhydrite laths included in megaquartz crystals and spherulitic fibrous quartz (quartzine‐lutecite), suggest an origin from previous anhydrite nodules. The anhydrite nodules at Laño were produced by the percolation of marine brines, during a period corresponding to a sedimentary gap, with δ³⁴S and δ¹⁸O mean values of 18.8‰ and 13.6‰ respectively, consistent with Upper Cretaceous seawater sulphate values. Higher δ³⁴S and δ¹⁸O mean values of 21.2‰ and 21.8‰ recorded in the Tubilla del Agua section are interpreted as being due to a partial bacterial sulphate reduction process in a more restricted marine environment. The idea that sulphates may have originated from the leaching of previously deposited Keuper sulphate evaporites with subsequent precipitation as anhydrite, is rejected because the δ³⁴S, δ¹⁸O and ⁸⁷Sr/⁸⁶Sr values of anhydrite laths observed at both the Tubilla del Agua and Laño sections suggest an origin from younger marine brines. Later calcite replacement and precipitation of geode‐filling calcite is recorded in both sections, with δ¹³C and δ¹⁸O values indicating the participation of meteoric waters. Synsedimentary activity of the Peñacerrada diapir, which lies close to the Laño section, played a significant role in the local shallowing of the basin and the formation of quartz geodes. In contrast, eustatic shallowing of the inner marine series of the Tubilla del Agua section led to the generation of morphologically similar quartz geodes. Copyright © 2002 John Wiley & Sons, Ltd.     

Variations of the Ca/Ca ratio in seawater during the past 24 million years: evidence from δCa and δO values of Miocene phosphates

The Ca isotope variation of 11 Miocene and Pleistocene, authigenic, marine phosphates is rather small compared to the corresponding variation in δ¹⁸O values. The δ⁴⁴Ca values are not correlated with the δ¹⁸O values and, therefore, they are not temperature controlled. It is likely that the δ⁴⁴Ca values of the phosphorites reflect the variation in the δ⁴⁴Ca values of paleo-seawater but, in contrast to Sr, not the isotopic composition of seawater itself. Furthermore, Ca and Sr isotopic compositions are decoupled with decreasing stratigraphic age of the phosphate peloids with Sr isotopic compositions changing to more radiogenic values while Ca isotopic compositions remain rather stable. All samples have δ⁴⁴Ca values below present-day seawater values, suggesting that phosphate formation discriminates against heavy Ca isotopes.Phosphorites and carbonaceous sediments have a similar Ca isotopic variation during the Miocene. A systematic and more or less constant shift between marine carbonates and phosphates is observed: the phosphate samples are slightly less enriched in ⁴⁰Ca compared to carbonates. This shift has been related to a mineral-dependent kinetic mass fractionation during precipitation from seawater. The rather stable δ⁴⁴Ca value for the 19 to 9 Ma old phosphorites points to a constant δ⁴⁴Ca fractionation of about 1.1 between seawater and phosphorites during the past and suggests steady-state conditions for the Mid-Miocene seawater (sedimentation flux equals erosion flux).     

美国怀俄明州拉那依段岩相及碳氧同位素地球化学特征

1980年6月,本文作者之一的K. Kelts曾去美国参加由经济古生物学者和矿物学者协会组织的地质旅行。该行主要是观察和研究怀俄明州西南始新统绿河组的沉积环境。对此次旅行中带回瑞士苏黎世联邦理工学院地质研究所的样品,曾作了切片、X-射线衍射和碳氧同位素分析。     

Modelling of the oxygen isotope evolution of seawater: implications for the climate interpretation of the δ18O of marine sediments

It is often argued that the δ¹⁸O value of oceanic water was maintained close to 0‰ for hundreds of millions of years, as a consequence of oxygen isotope exchange between oceanic crust and seawater. However, for several decades, the interpretation of the biosedimentary oxygen isotope record has conflicted with the igneous record because, with increasing age, a general trend of decreasing δ¹⁸O values (about 6‰) is observed in most carbonates, cherts and phosphates, especially for the Paleozoic and early Mesozoic. We developed a dynamical model of seawater-crust interaction that computes the δ¹⁸O value in these two reservoirs as function of time. This model takes into account the continuous production of crust at oceanic ridges, its expansion rate, the permeability profile with space and time, the mineralogical mode of the crust, and the kinetics of oxygen isotope exchange between rock-forming minerals and seawater. The model indicates that the δ¹⁸O value of seawater may vary by ±2‰ with a time response ranging from 5 to 50 Ma for expansion rates of 1 to 10 cm.a⁻¹. The variation of ±2‰ is fixed by both integrated water-rock ratio and closure time of the seawater-crust system by sediments. Variations in the oxygen isotope ratio of seawater through time have important implications for the interpretation of the systematically low δ¹⁸O values of pre-Jurassic marine sediments. According to our model, marine paleotemperatures could be up to 10°C lower than those expected when applying the classical hypothesis of an ice-free ocean with a δ¹⁸O value of −1‰.     

Late Miocene nonmarine sedimentation and formation of magnesites in the Acıgöl Basin, southwestern Anatolia, Turkey

The Late Miocene lacustrine Acıgöl Basin, SW Turkey, formed as an orogen-top, extensional half-graben, with the subaqueous accommodation controlled by the lake level and the bulk accommodation provided by active subsidence along a WSW-trending normal fault at the basin's southern margin. The basin-fill sedimentary succession consists of terminal alluvial-fan facies overlain by ephemeral lake-margin facies and perennial lake facies, with widespread fluvial facies at the top. The distal alluvial-fan facies include massive to stratified sandstones and massive mudstones with intervening nodular dolostones and incipient pedogenic horizons. The lake-margin facies are micritic magnesites passing laterally into peloidal, irregularly laminated magnesites towards the palaeolake margin and overlain by marlstones and dolostones, all with abundant evidence of episodic subaerial exposure (desiccation cracks, pedogenic features, and tepee structures). The perennial lake facies are micritic magnesites passing upwards into clayey dolostones and dolomitic or clayey marlstones. The fluvial facies capping the succession include planar cross-stratified conglomerates (channel-fill deposits), planar parallel-stratified, planar cross-stratified and rippled cross-laminated sandstones (crevasse-fill and crevasse splay deposits), and assemblages of mudstones intercalated with thin sandstone beds (overbank floodplain deposits).The sedimentological, mineralogical and geochemical data reveal large variations in the basin's hydrological regime, including short-term oscillations and bulk rise of the lake level, periodical changes in the Mg/Ca ratio and terrigenous mud supply, and a negative covariance of δ¹⁸O and δ¹³C fluctuations. The composition of terrigenous sediment and the chemistry of water supplied to the lake were controlled by the weathering, chemical leaching and erosion of the ultramafic–dolomitic bedrock in the catchment area. The bedrock yielded Mg-rich carbonate solutions that caused the deposition of Mg-carbonates in the lake.Despite short-term lake-level fluctuations, the lake's net water budget remained positive. It is suggested that the region's present-day climate and Mg-rich alkaline lakes can serve as an analogue for the climatic and hydrological conditions in the Late Miocene Acıgöl Basin.     

生物标志物稳定氢同位素研究进展及在海洋古环境重建中的应用

生物标志物稳定氢同位素是一种比较新的古环境指标,越来越多的研究者利用生物标志物稳定氢同位素重建了陆地和海洋中古水循环的变化。在陆地上,生物标志物δD值可以用来重建降雨δD值、古海拔以及蒸散作用大小或者湖泊水的输入输出平衡。在海洋中,生物标志物δD值的变化能更好地反映与其相关的生物和环境信息。培养实验以及现场数据显示生物标志物δD值能很好地反映表层海水δD值以及表层海水盐度的变化。许多研究者也利用海洋中生物标志物δD值重建了长时间尺度降雨量以及表层海水盐度的变化。对近年来生物标志物稳定氢同位素的研究进展,尤其是在海洋古环境重建中的应用进行了总结。     

Organic petrography and geochemistry of inertinite-rich mudstones, Jakobsstigen Formation, Upper Jurassic, northeast Greenland: Indications of forest fires and variations in relative sea-level

The lower-middle Oxfordian Jakobsstigen Formation, Wollaston Forland, northeast Greenland, consists mainly of stacked coarsening-upward successions of offshore to shoreface heteroliths, sandstone and rare foreshore sandstones. The units are separated by thin, laterally extensive sheets of terrigenous carbonaceous mudstones, which have been subjected to organic petrographic and geochemical studies. The mudstones are thermally immature, with maturities corresponding to R₀ in the range 0.35–0.50%. The mudstones contain very high proportions of allochthonous inertinite, subordinate huminite, char and negligible proportions of liptinite. Inertinite reflectance distributions are markedly bimodal, with maxima at approximately 1.73 and 4.91% R_m. Both pyrolysis yields and solvent extract yields are low. The distributions of n-alkanes are markedly light-end skewed and show a pronounced predominance of even-numbered compounds in the lower carbon number range. Biomarker-distributions feature a dominance of C₂₉-steranes, slight enhancement of extended hopanes and αββ-steranes, low proportion of tricyclic triterpanes and very low hopane/sterane ratios. Sedimentological, organic petrographical and geochemical evidence suggests that the regular alternation between marine and terrestrial depositional environments during deposition of the Jakobsstigen Formation was related to low-amplitude, high-frequency changes in relative sea-level and local climate. The mudstones were deposited during early rise of relative sea-level in shallow, flat-bottomed lakes or lagoons on a broad coastal plain. The lakes acted as traps for fine elastic sediment and for predominantly windborne inertinite, generated by wildfires in the hinterland. High rates of evaporation rendered the lakes mildly saline, hampering their colonization by vegetation other than cyanobacteria and halophilic microorganisms. Similarly, saline porewaters excluded higher plant vegetation from emergent areas. Upon continued rise of the relative sea-level, the lakes were gradually flooded and their deposits became covered by sandy shallow marine sediments. The larger areas covered by shallow marine waters during periods of high relative sea-level led to a more humid local climate and to lower frequency of wildfires. During falling relative sea-level, the marine deposits were eroded and partially removed and the cycle subsequently repeated upon renewed rise in relative sea-level. Hence, minor changes in relative sea-level gave rise to the regular alternation of two vastly different depositional environments, as well as to marked variations in local climate.     

Heterogeneous Mg isotopic composition of the early Carboniferous limestone: implications for carbonate as a seawater archive

Carbonate precipitation and hydrothermal reaction are the two major processes that remove Mg from seawater. Mg isotopes are significantly (up to 5‰) fractionated during carbonate precipitation by preferential incorporation of ²⁴Mg, while hydrothermal reactions are associated with negligible Mg isotope fractionation by preferential sequestration of ²⁶Mg. Thus, the marine Mg cycle could be reflected by seawater Mg isotopic composition (δ²⁶Mg_sw), which might be recorded in marine carbonate. However, carbonates are both texturally and compositionally heterogeneous, and it is unclear which carbonate component is the most reliable for reconstructing δ²⁶Mg_sw. In this study, we measured Mg isotopic compositions of limestone samples collected from the early Carboniferous Huangjin Formation in South China. Based on petrographic studies, four carbonate components were recognized: micrite, marine cement, brachiopod shell, and mixture. The four components had distinct δ²⁶Mg: (1) micrite samples ranged from ?2.86‰ to ?2.97‰; (2) pure marine cements varied from ?3.40‰ to ?3.54‰, while impure cement samples containing small amount of Rugosa coral skeletons showed a wider range (?3.27‰ to ?3.75‰); (3) values for the mixture component were ?3.17‰ and ?3.49‰; and (4) brachiopod shells ranged from ?2.20‰ to ?3.07‰, with the thickened hinge area enriched in ²⁴Mg. Due to having multiple carbonate sources, neither the micrite nor the mixture component could be used to reconstruct δ²⁶Mg_sw. In addition, the marine cement was homogenous in Mg isotopes, but lacking the fractionation by inorganic carbonate precipitation that is prerequisite for the accurate determination of δ²⁶Mg_sw. Furthermore, brachiopod shells had heterogeneous C and Mg isotopes, suggesting a significant vital effect during growth. Overall, the heterogeneous δ²⁶Mg of the Huangjin limestone makes it difficult to reconstruct δ²⁶Mg_sw using bulk carbonate/calcareous sediments. Finally, δ²⁶Mg_sw was only slightly affected by the faunal composition of carbonate-secreting organisms, even though biogenic carbonate accounts for more than 90% of marine carbonate production in Phanerozoic oceans and there is a wide range (0.2‰–4.8‰) of fractionation during biogenic carbonate formation.     

A regressive coastal sequence from the Upper Eocene of Hampshire, southern England

The Lower Headon and Upper Barton Beds of Hampshire, southern England, consist of fine sands, silts and clays, often fossiliferous, with lignitic and carbonate horizons. They accumulated in a coastal environment following deposition of the marine Lower and Middle Barton Beds. A variety of distinctive facies can be defined on faunal and lithological grounds, and these permit palaeoenvironments to be defined with some precision. Littoral marine, barrier island shoreface, storm washover and barrier flat, brackish lagoon, distributary channel and floodplain lake environments are recognized. The evidence suggests that a barrier island or spit developed offshore, enclosing a sheltered inshore region of lagoons in which deposition of relatively fine-grained sediments took place. Lagoonal sediments show a general trend towards reduction of salinity with time. With the eventual exclusion of marine influence, the area underwent a gradual transition to river-dominated sedimentation in shallow flood-plain lakes. While the sequence as a whole shows a progressive reduction in salinity, several brief periods of increased salinity are recognized and these reflect the very low topography of the region and its susceptibility to marine incursion.