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1.
Holocene beachrocks of Northeast Brazil are composed predominantly of quartz (90%) with minor carbonate fragments (6% algal detritus) and feldspars (4%). The cement shows three textural varieties: (1) calciferous, surrounding siliciclastic grains; (2) micritic, with an acicular fringe; and (3) cryptocrystalline calcite in pores. Sandstone structures and composition show evidence of submerged and low-energy beaches. Cement is formed by ～20 mol% MgCO3; the δ13C in cement ranges from ?1.3‰ to +3.5‰ PDB and δ18O varies from ?2.1 to +1.2‰PDB. The cement was precipitated under high CO2 pressure, as a result of the interaction of CaCO3? saturated seawater and nonsaturated groundwater, in a beach environment.  相似文献   

2.
Limestone consisting of finely to medium crystalline calcite mosaics is present in the upper part of the Winnipegosis Formation on the east‐central margin of the Elk Point Basin where the overlying Prairie Evaporite deposits have been removed. This type of crystalline limestone is interpreted as dedolomite, based on petrographic observations. The δ18O and δ13C values of the Winnipegosis dedolomite vary from ?12·8‰ to ?11·9‰ VPDB (Vienna Pee Dee Belemnite) and from ?0·5‰ to +1·7‰ VPDB, respectively; both values are significantly lower than those for the corresponding dolomite. The 87Sr/86Sr ratios of the dedolomite are significantly higher, between 0·7082 and 0·7087. The spatial distribution and geochemical data of the Winnipegosis dedolomite suggest that dedolomitization was related to an influx of fresh groundwater and dissolution of the Prairie Evaporite anhydrite during the latest Mississippian to the Early Cretaceous when the basin was subjected to uplift and erosion. The Winnipegosis dedolomite displays a series of replacement fabrics showing progressive calcitization of dolomite, including the occurrence of dedolomite restricted along fractures and adjacent areas, dolomite patches ‘floating’ in the dedolomite masses and massive dedolomite with sparsely scattered dolomite relicts. However, the characteristic fabrics resulting from dedolomitization documented in the literature have not been observed in the Winnipegosis dedolomite. Coarsely to very coarsely crystalline, subhedral to euhedral calcite cement is restricted in the dedolomite. The petrographic features, isotopic compositions and homogenization temperatures, coupled with the burial history of the Winnipegosis Formation, constrain the precipitation of the calcite cement from a mixing of basinal brines and fresh groundwater during Late Cretaceous to Neogene time. The more negative C‐isotopic signatures of the calcite cement (?5·3‰ to ?2·3‰ VPDB) probably reflect a hydrocarbon‐derived carbon.  相似文献   

3.
Zoned calcites were found in the phragmacone chambers of three Sonniniid ammonites from marine Middle Jurassic sandstones (Isle of Skye, U.K.). Each ammonite has a unique sequence of up to nine zones of calcite which fill or partially fill the chambers. Zones are defined by changes in the density of minute opaque inclusions and variation in trace-element composition. Proximal (early) calcites have undulose extinction and some exhibit the specific fabrics of fascicular-optic and radiaxial fibrous calcites. Microdolomite inclusions are found in one specimen. Early calcites, interpreted as replacements after a single isopachous fringe of acicular carbonate (probably high magnesium calcite), are succeeded by blocky ferroan calcite cement. In one specimen there are two distinct generations of calcite, in the others there is a continuous mosaic incorporating both early calcites and late cement. Isotopic composition of the early calcite zones demonstrates the initial importance of organic derived carbon (δ13C =— 26‰, δ18O ‰ O). Further cementation and mineralogical stabilization took place at increased temperatures and probably after modification of the pore water isotopic composition (calcites with δ13C =— O‰, δ18O～— 10‰). The distinctive fabrics and zonal patterns probably developed during the replacement of the precursor cement and are not primary growth features. Reversals in isotopic and trace element trends are believed to be related to the rate of neomorphic crystal growth and hence to the degree of exchange with external pore waters. Further increase in temperature, probably during Tertiary igneous activity, gave rise to the extremely light δ18O values of the late cements in the ammonite which had previously had least contact with external waters (cements with δ13C ～ O, δ18O ～— 20‰).  相似文献   

4.
The sandbodies of the Bearreraig Sandstone Formation (Inner Hebrides, UK) are cemented by two generations of calcite. The first generation, an inhomogeneous ferroan calcite (0.05?3.28 mol% FeCo3) formed during sulphate reduction (δ13C =?24 to ?32%o PDB) in marine porewaters (δ18O of cement from ?1 to ?4%o PDB) at very shallow burial depths (a few centimetres). These cements are rare but form millimetre-scale clusters of crystals which acted as nuclei to the later, concretionary cements. The second generation of cements are more homogeneous ferroan calcites (mean 1?58% mol% FeCo3) which evolve to progressively higher Fe/Mg ratios. They are sourced by shell dissolution (δ13C of cement from +1 to ?3%o PDB) into meteoric (δ18O of cement from ?6 to ?10%o PDB) or mixed marine meteoric waters (δ18O of cement from ?4 to ?6%o SMOW). These were introduced into the formation either during Bathonian times as a freshwater lens, or, subsequent to partial inversion, by confined aquifer flow. Corroded feldspars within the concretions suggest that an interval of at least 8 Ma separated the deposition of the sediments from the onset of concretion growth. Abundant concretions are preferentially developed at certain horizons within the sandbodies, where the early generation of ferroan calcite cements provided nuclei. The latter formed close to the sediment-water interface, the concentration of cement within the sediment being related to sedimentation rate. The relatively high concentrations of the first generation of cement, upon which the concretionary horizons are nucleated, formed during periods of minimal sedimentation.  相似文献   

5.
Salt-rich soft soils have not only general characteristics of common soft soils, but also contain high contents of Mg2+, Cl?, and SO42?, which have negative effects on deep mixing method using cement to treat soft soils. Laboratory and field tests were conducted to investigate the effects of changing cement incorporating ratio, water content, cement mixing ratio, and contents of Mg2+, Cl?, and SO42? on the unconfined compressive strength of the salt-rich soil–cement. The microstructure of soil–cement and the mechanism for the strength change of salt-rich soil–cement were investigated using X-ray diffraction, scanning electronic microscopy (SEM), and backscattered diffraction technology. It was found that an increase of cement incorporating ratio enhanced the strength of soil–cement but reduced its strength when water is added. Different amounts of Mg2+, Cl?, and SO42? not only caused the difference in the microstructures of salt-rich soil–cement but also influenced the soil–cement strength.  相似文献   

6.
Geochemical and petrographic data suggest early submarine cementation of hardgrounds from the Lincolnshire Limestone Formation, Middle Jurassic, England. The three hardgrounds, from Cowthick, Castle Bytham and Leadenham quarries, developed in tidal-inlet, on-barrier and lagoonal sub-environments of a carbonate barrier-island complex. At Cowthick early composite (acicular-bladed) radial-fibrous cements, which pre-date aragonite dissolution, completely fill intergranular pore-space at the hardground surface; away from it isopachous fringing cements decrease in thickness. Microprobe analyses demonstrate zoning within the fringes with magnesium concentrations (> 2 wt % MgCO3) higher than those in allochems or later, ferroan cement (?0.5 wt % MgCO3, 1.7 wt % FeCO3). At Castle Bytham early granular isopachous cements, which post-date aragonite dissolution, occur within 5 cm of the surface. At Leadenham early lithification is superficial and represented by ferruginous crusts and micritic internal sediment. Late blocky cement fills residual pore-space in all three examples. Carbon and oxygen isotopic composition of whole-rock samples taken at intervals away from each hardground surface demonstrate the increasing proportion of late 18O depleted cements (δ18O – 8 to – 10). Early cements must have a marine isotopic composition; different δ18O values from each hardground reflect the intensity of early lithification and exclusion of late cements at the hardened surface. There is no isotopic evidence for subaerial cement precipitation during possible emergence at Castle Bytham. Oyster samples (with δ18O, – 2.9 and δ13C, 2.4) give estimated palaeotemperatures of 22–25°C. Early cements from Cowthick are enriched in 18O and 13C (δ18O = 0 δ13C ? 3‰) compared to the oyster values. In conjunction with trace element data this is interpreted as evidence for high-magnesium calcite precursor cements which underwent replacement in a system with a low water: rock ratio. The intensity of early lithification is related to depositional environment: maximum circulation of sea-water producing the most lithified hardground (Cowthick). This is directly analogous to the formation of Recent hardgrounds.  相似文献   

7.
Dendritic calcite forms in an active cold-water tufa system in association with extracellular polymeric substances (EPS) that discontinuously coat bryophytes and cyanobacteria. Dendrites consist of 100–200 nm thick calcite fibres that form 3D lattice-like domains. In each dendrite domain, fibres have three structurally equal orientations, which correspond in disposition to radii from the centre of a calcite unit cell to the convex triple face junctions on its surface. Fibres do not form in the orientation of the c-axis. The external form of each dendrite has the shape of half of a shortened octahedron, with an upper triangular surface parallel to the substrate. Dendrite nucleation takes place on or in microbial EPS, whether microbial cells are present or not, and is probably effected by attraction of Ca2+ cations to negatively charged EPS, together with CO2-degassing and concomitant pH increase of supersaturated spring water in stream splash zones. Ensuing dendrite growth is abiogenic and controlled by diffusion. Dendrite c-axes are perpendicular to the substrate, probably because the negative charge of EPS forces the orientation of Ca2+ and CO planes within the developing dendrite crystal to be parallel to the EPS film surface. Dendrites are eventually filled and overgrown by solid, syntaxial calcite, which gradually and completely obliterates the dendrites as more familiar calcite crystal forms develop. No trace of the dendritic nucleus remains in the rock record. Calcite crystal nucleation may take place by this mechanism in many marine and meteoric settings, given that microbial EPS is now assumed to be virtually ubiquitous in these environments. This phenomenon could contribute to the development of familiar fabrics such as marine micrite cement and fibrous calcite cement, radial ooids, peloids, ‘abiogenic’ stromatolites, sea floor precipitates, microbialites, tufa, travertine, speleothems, and some meteoric cements. It may also contribute to the substrate-normal orientation of c-axes of common cement fabrics.  相似文献   

8.
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 (δ26Mgsw), 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 δ26Mgsw. 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 δ26Mgsw. 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 δ26Mgsw. 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 δ26Mgsw using bulk carbonate/calcareous sediments. Finally, δ26Mgsw 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.  相似文献   

9.
Quartz from sandstone‐type uranium deposits in the east part of the Ordos Basin contains abundant secondary fluid inclusions hosted along sealed fractures or in overgrowths. These inclusions consist mainly of water with NaCl, KCl, CO2 (135–913 ppm) and trace amounts of CO (0.22–16.8 ppm), CH4 (0.10–1.38 ppm) and [SO4]2? (0.35–111 ppm). Homogenization temperatures of the studied fluid inclusions range from 90 to 210°C, with salinities varying from 0.35 to 12.6 wt‐% (converted to NaCl wt%), implying multiple stages of thermal alteration. Although high U is associated with a high homogenization temperature in one case, overall U mineralization is not correlated with homogenization temperature nor with salinity. The H and O isotopic compositions of fluid inclusions show typical characteristics of formation water, with δ18O ranging from 9.8 to 12.3‰ and δD from 26.9 to ?48.6‰, indicating that these fluid inclusions are mixtures of magmatic and meteoric waters. The oxygen isotope ratios of carbonates in cement are systematically higher than those of the fluid inclusions. Limited fluid inclusion‐cement pairs show that the oxygen closely approaches equilibrium between water and aragonite at 150°C. Highly varied and overall negative δ13C in calcite from cement implies different degrees of biogenetic carbon involvement. Correlations between U in bulk rocks and trace components in fluid inclusions are lacking; however, high U contents are typically coupled with high [SO4]2?, implying pre‐enrichment of oxidized materials in the U mineralization layer. All these relationships can be plausibly interpreted to indicate that U (IV), [SO4]2? as well as Na, K were washed out from the overlying thick sandstone by oxidizing meteoric water, and then were reduced by reducing agents, such as CH4 and petroleum, likely from underlying coal and petroleum deposits, and possibly also in situ microbes at low temperatures.  相似文献   

10.
The Pennsylvanian phylloid algal mounds exposed in the Cervatina Limestone of the Cantabrian Zone (NW Spain) developed during the highstands of high-frequency shallowing-upward cycles and lack evidence of subaerial exposure at their tops. Mound core facies are composed of massive bafflestones with variable amounts of calcite cements and anchicodiacean phylloid algae with cyathiform thalli preserved in growth position. Through standard petrographic, isotopic (δ18O and δ13C), major and trace element (Ca, Mg, Fe, Mn, Sr) and cathodoluminescence analyses, five calcite cement phases (cement 1 (C1)–cement 5 (C5)) have been identified filling primary and secondary pores. Early marine diagenesis is represented by micritization and non-luminescent to mottled-dull luminescent high-Mg calcite fibrous marine cement (C1). A dissolution phase then occurred and created vuggy and moldic pores. Based on the absence of field or petrographical or geochemical evidence of exposure, it is inferred that dissolution occurred in near-surface undersaturated marine waters with respect to aragonite related to progressive organic matter oxidation. Secondary porosity was subsequently filled by dull-bright-dull bladed high-Mg calcite (C2), which precipitated in the early shallow burial from marine-derived pore waters. Remaining porosity was occluded by shallow-burial precipitates consisting of non-luminescent scalenohedral low-Mg calcite (C3) followed by non-ferroan dull luminescent calcite spar (C4). Latter phases of calcite spar exhibiting non- and dull luminescence (C5) are associated with burial calcite veins. Low δ18O values (around ?8‰), moderately depleted δ13C values (around 0.5‰) and the homogeneity of trace element contents of carbonate matrix, cements and vein-filling calcites suggest burial isotopic re-equilibration and recrystallization, probably in Early Permian times during post-thrusting orocline formation.  相似文献   

11.
为研究鄂尔多斯盆地上三叠统延长组长81亚油层组沉积微相与储层物性的关系,通过岩心相、测井相及物性等资料,结合前人研究成果,对盆内合水地区长81亚油层组进行分析。认为:(1)长81亚油层组浅水三角洲前缘沉积发育水下分流河道、河口坝、前缘席状砂、分流间湾4种沉积微相。多期叠置的水下分流河道是控制砂体发育的主要微相类型,根据砂地比又可分为河道核部、河道中部及河道侧翼;(2)长812小层水下分流河道砂体发育频率较高、沉积期次较多、连通性较强,其次为长8812小层与长813小层;(3)由沉积微相决定的岩石结构成熟度控制了储层的初始孔隙度,进而在一定程度上影响了储层现今孔隙度。水下分流河道核部储层物性最好,是有利微相类型。研究区长812小层有利微相发育规模最大,为后期勘探开发首要目的层位。  相似文献   

12.
The most ubiquitous syn-sedimentary cements affecting Mururoa atoll are composed of magnesian calcite. Three main types are distinguished: fibrous, bladed and sparitic on the basis of petrography, morphology and MgCO3 concentration of the constituting crystals, while peloid infills, a particular form of HMC chemical precipitation, also exist. Petrographic evidence and isotopic signatures are compatible with marine precipitation. Mururoa atoll was exposed several times to meteoric diagenesis resulting in varied diagenetic alterations including selective dissolution and partial dolomitization of Mg-calcite cements. These alterations are responsible for substantial modifications of the initial cement fabrics and may introduce unconformities in the diagenetic chronology. The first stage of the partial dissolution of Mg-calcite induces the development of chalky, white friable zones within the initially crystalline, hard cement layers. At ultrascale, this is due to the creation of micro-voids along the elongate cement fibres. Advanced dissolution includes total disappearance of cement portions as attested to by large voids within the cement crust and/or between superposed cement layers. Mg-calcite dissolution is related to meteoric diagenesis during periods of Quaternary exposure. The creation of voids within Mg-calcite layers is due to the mechanical removal of previously altered calcium carbonate, a process suggesting marine or non-marine water flow, probably in the vadose environment. Selective dolomitization of Mururoa cements involves alternations of calcite and dolomite which form successive cement-like rinds within primary cavities. At Mururoa, these alternations are the result of selective dolomitization of the pre-existing Mg-calcite cements rather than successive precipitation of calcite and dolomite. Selective dolomitization of Mg-calcite cements at Mururoa indicates that a given cement succession is not necessarily a simple chronological sequence. Oxygen isotope values of dolomites are enriched in δ186 by about 3‰ PDB within calcite-dolomite pseudo-alternations. The dolomitizing fluid at Mururoa seems similar to present marine water although some mixture with meteoric water is probable to favour dissolution associated with dolomitization.  相似文献   

13.
In this study, the stable isotope and trace element geochemistries of meteoric cements in Pleistocene limestones from Enewetak Atoll (western Pacific Ocean), Cat Island (Bahamas), and Yucatan were characterized to help interpret similar cements in ancient rocks. Meteoric calcite cements have a narrow range of δ18O values and a broad range of δ13C values in each geographical province. These Pleistocene cements were precipitated from water with stable oxygen isotopic compositions similar to modern rainwater in each location. Enewetak calcite cements have a mean δ18O composition of ?6.5%0 (PDB) and δ13C values ranging from ?9.6 to +0.4%0 (PDB). Sparry calcite cements from Cat Island have a mean δ18O composition of ?4.1%0 and δ13C values ranging from ?6.3 to + 1.1%0. Sparry cements from Yucatan have a mean δ18O composition of ?5.7%0 and δ13C values of ?8.0 to ?2.7%0. The mean δ18O values of these Pleistocene meteoric calcite cements vary by 2.4%0 due to climatic variations not related directly to latitude. The δ13C compositions of meteoric cements are distinctly lower than those of the depositional sediments. Variations in δ13C are not simply a function of distance below an exposure surface. Meteoric phreatic cements often have δ13C compositions of less than —4.0%0, which suggests that soil-derived CO2 and organic material were washed into the water table penecontemporaneous with precipitation of phreatic cements. Concentrations of strontium and magnesium are quite variable within and between the three geographical provinces. Mean strontium concentrations for sparry calcite cements are, for Enewetak Atoll, 620 ppm (σ= 510 ppm); for Cat Island, 1200 ppm (σ= 980 ppm); and for Yucatan, 700 ppm (σ= 390 ppm). Equant cements, intraskeletal cements, and Bahamian cements have higher mean strontium concentrations than other cements. Equant and intraskeletal cements probably precipitated in more closed or stagnant aqueous environments. Bahamian depositional sediments had higher strontium concentrations which probably caused high strontium concentrations in their cements. Magnesium concentrations in Pleistocene meteoric cements are similar in samples from Enewetak Atoll (mean =1.00 mol% MgCO3; σ= 0.60 mol% MgCO3) and Cat Island (mean = 0.84 mol% MgCO3; σ= 0.52mol% MgCO3) but Yucatan samples have higher magnesium concentrations (mean = 2.20 mol% MgCO3: σ= 0.84mol% MgCO3). Higher magnesium concentrations in some Yucatan cements probably reflect precipitation in environments where sea water mixed with fresh water.  相似文献   

14.
Three categories of fibrous calcite from early to middle Caradoc platform-marginal buildups in east Tennessee can be delineated using cathodoluminescent microscopy, minor element chemistry and stable C-O isotopic composition. Bright luminescent fibrous cement has elevated Mn (>1000 p.p.m.), negative δ13C and intermediate δ18O values relative to other types of fibrous calcite. This cement reflects fibrous calcite that interacted with reducing Mn-rich fluids. Dully luminescent fibrous cement has elevated Fe (>400 p.p.m.), positive δ13C and negative δ18O values relative to other fibrous cements. This cement was stabilized by burial fluids. Nonluminescent fibrous cement has low Mn and Fe (generally below 400 p.p.m.) and positive δ13C and δ18O values relative to other types of fibrous calcite. The latter cement is interpreted to be the best material for determining the isotopic composition of calcite precipitated in equilibrium with early to middle Caradoc seawater, which is δ13C=1% PDB and δ18O=?4 to ?5‰ PDB. Results from this study and Ashgillian brachiopods indicate that the average δ18O composition of the Ordovician ocean, during nonglacial periods, was probably never more negative than ?3‰ SMOW. Assuming an Ordovician seawater δ18O value of ?1‰ SMOW, Holston Formation fibrous cements would have precipitated at temperatures between 27 and 36 °C, which is near the upper temperature limit for metazoans. A seawater δ18O value of ?2‰ SMOW yields temperatures ranging from 23 to 31 °C, while a ?3‰ SMOW value yields temperatures of 18–26 °C.  相似文献   

15.
Caliche is a fairly widespread pedogenic carbonate that commonly has been used to reconstruct palaeoclimatological conditions. Stable isotopic analyses of three types of caliche nodules from Mission Bay, Texas, provide insights into the values and limitations in palaeoenvironmental interpretations. Soft incipient nodules (type I) and partially lithified chalky nodules (type II), composed of low Mg‐calcite, are in situ pedogenic products in the late Quaternary soils; they represent young to intermediate caliche nodules with no obvious diagenesis and, with constraints, can be used to investigate palaeoenvironmental conditions. The well‐lithified hard nodules (type III) dispersed on the beach and shallow bay exhibit complex shapes, fabrics, mineralogy and geochemical compositions. They are mature nodules that have undergone substantial diagenesis and, therefore, are believed to have lost their initial environmental signatures. The incipient nodules in the presently active grey soil and the older subjacent brown soil display significantly different δ13C values, ?8·4 and ?4·4‰, respectively, which indicates a change in palaeovegetation from C3/C4 mixed to C3‐dominated flora. The δ13C values probably reflect a marked climate shift from warm and dry to cool and wet conditions in the middle Holocene. However, in the same grey soil, there is a sub‐set of incipient caliche nodules with δ13C values around 0·1‰, which is probably due to the input of localized carbon sources in the soil (e.g. shell fragments). The occurrence of essentially identical nodules appearing from the same modern soil horizon with significantly different δ13C values questions the universal reliability of this type of data for palaeoenvironmental interpretation. This study demonstrates that, whereas the stable isotopic compositions of caliche nodules can be used for palaeoenvironmental reconstruction, diagenesis and the influence of localized carbonate sources in the soils could lead to erroneous interpretations.  相似文献   

16.
Petrography demonstrates the presence of three types of fibrous calcite cement in buildup deposits of the Kullsberg Limestone (middle Caradoc), central Sweden. Translucent fibrous calcite has intrinsic blue luminescence (CL) indicative of pure calcite. This cement has 2–5 mol% MgCO3, low Mn and Fe (≤ 100 p.p.m.), and is considered to be slightly altered to unaltered, primary low- to intermediate-Mg calcite. Grey turbid fibrous calcite has variable but generally low MgCO3 content (most analyses <2 mol%) and variable CL response, with Mn and Fe concentrations up to 1200 and 500 p.p.m., respectively. The heterogeneous characteristics of this variety of fibrous calcite are caused by diagenetic alteration of a translucent fibrous calcite precursor. Light-brown turbid fibrous calcite has low MgCO3 (near 1 mol%) and variable Mn (up to 800 p.p.m.) and Fe (up to 500 p.p.m.) concentrations, with an abundance of bright luminescent patches, which formed during alteration caused by reducing diagenetic fluids. The δ13C and δ18O values of all fibrous calcite form a tight field (δ13C=1·7 to 3·1‰ PDB, δ18O= ? 2·6 to ? 4·1‰ PDB) compared with fibrous calcite isotope values from other units. Fibrous calcite δ18O values are larger than adjacent meteoric or burial cements, which have δ18O δ ? 8‰ PDB. Consequently, most diagenetic alteration of Kullsberg fibrous calcite is interpreted to have occurred in the marine diagenetic realm. First-generation equant and bladed calcite cements, which pre-date fibrous calcite, are interpreted as unaltered, low-Mg calcite marine cements based on δ13C and δ18O data (δ13C = 2·3 to 2·7‰ PDB, δ18O= ? 2·8 to ? 3·5‰ PDB). Unlike fibrous cement, which reflects global sea water chemistry, first-generation equant and bladed calcite are indicators of localized modification of seawater chemistry in restricted settings. Kullsberg abiotic marine cements have larger δ18O values than most Caradoc marine precipitates from equatorial Laurentia. Positive Kullsberg δ18O values are attributed to lower seawater temperatures and/or slightly elevated salinity on the Baltic platform relative to seawater from which other marine precipitates formed.  相似文献   

17.
During Integrated Ocean Drilling Program Expedition 325, 34 holes were drilled along five transects in front of the Great Barrier Reef of Australia, penetrating some 700 m of late Pleistocene reef deposits (post‐glacial; largely 20 to 10 kyr bp ) in water depths of 42 to 127 m. In seven holes, drilled in water depths of 42 to 92 m on three transects, older Pleistocene (older than last glacial maximum, >20 kyr bp ) reef deposits were recovered from lower core sections. In this study, facies, diagenetic features, mineralogy and stable isotope geochemistry of 100 samples from six of the latter holes were investigated and quantified. Lithologies are dominated by grain‐supported textures, and were to a large part deposited in high‐energy, reef or reef slope environments. Quantitative analyses allow 11 microfacies to be defined, including mixed skeletal packstone and grainstone, mudstone‐wackestone, coral packstone, coral grainstone, coralline algal grainstone, coral‐algal packstone, coralline algal packstone, Halimeda grainstone, microbialite and caliche. Microbialites, that are common in cavities of younger, post‐glacial deposits, are rare in pre‐last glacial maximum core sections, possibly due to a lack of open framework suitable for colonization by microbes. In pre‐last glacial maximum deposits of holes M0032A and M0033A (>20 kyr bp ), marine diagenetic features are dominant; samples consist largely of aragonite and high‐magnesium calcite. Holes M0042A and M0057A, which contain the oldest rocks (>169 kyr bp ), are characterized by meteoric diagenesis and samples mostly consist of low‐magnesium calcite. Holes M0042A, M0055A and M0056A (>30 kyr bp ), and a horizon in the upper part of hole M0057A, contain both marine and meteoric diagenetic features. However, only one change from marine to meteoric pore water is recorded in contrast with the changes in diagenetic environment that might be inferred from the sea‐level history. Values of stable isotopes of oxygen and carbon are consistent with these findings. Samples from holes M0032A and M0033A reflect largely positive values (δ18O: ?1 to +1‰ and δ13C: +1 to +4‰), whereas those from holes M0042A and M0057A are negative (δ18O: ?4 to +2‰ and δ13C: ?8 to +2‰). Holes M0055A and M0056A provide intermediate values, with slightly positive δ13C, and negative δ18O values. The type and intensity of meteroric diagenesis appears to have been controlled both by age and depth, i.e. the time available for diagenetic alteration, and reflects the relation between reef deposition and sea‐level change.  相似文献   

18.
Water quality in the Maryland/Virginia Coastal Bays has been declining for many years from anthropogenic inputs, but conditions appear to have worsened abruptly following a shift from long-term dry to long-term wet conditions in the early 2000s. Annually and regionally averaged total nitrogen concentrations are approximately twofold higher, but ammonium (NH4 +) concentrations are up to an order of magnitude higher than in the early 1990s. Averaged nitrate concentrations, however, changed to a lesser degree throughout the time course; water column concentrations remain very low. Total phosphorus has only increased in some bay segments, but increases in phosphate (PO4 3?) have been more pervasive. There were differences in the year in which large increases in each nutrient were first noted: PO4 3? in ~2001–2002, followed by NH4 + ~a year later. The effects of a combination of steadily increasing anthropogenic nutrient increases from development, superimposed on nutrient loads from farming and animal operations, and groundwater inputs were accelerated by changes in freshwater flow and associated, negatively reinforcing, biogeochemical responses. Regionally, chlorophyll a concentrations have increased, and submersed aquatic vegetation has decreased. The system is now characterized by sustained summer picoplanktonic algal blooms, both brown tide and cyanobacteria. The retentive nature of this coastal lagoon combined with the reducing nature of the system will make these changes difficult to reverse if the current dual nutrient management practices are not accelerated.  相似文献   

19.
Unusually large biogenic sedimentary structures from the shallow quiescent-marine siliciclastics of the Upper Eocene Birket Qarun Formation in the Fayum area of Egypt display pronounced concretion formation around the trace fossils. The structures are massive, and vary morphologically, forming branched pillars (up to dm-scale), vertical (up to 180 cm height) amphora-like masses, and 3-D box-work “maze”. Bioturbation, mainly Thalassinoides attributable to the Glossifungites ichnofacies, mediated and modified the physical and chemical microenvironments influencing early diagenesis; i.e., burrows promote the precipitation of pervasive calcite-dominated cement. The inferred paragenesis, combined with the negative (light) carbon and oxygen stable-isotopic values of the bulk calcite (δ13CPDB from ?0.94 to ?4.98‰ and δ18OPDB from ?4.63 to ?7.22‰) and bulk dolomite (δ13CPDB from ?2.05 to ?8.23‰ and δ18OPDB from ?1.41 to ?11.20‰), imply that the pore-water carbon was derived directly from seawater and dissolution of metastable carbonate, which was mediated by bacterial decomposition of organic matter and mixing of meteoric ground water. Thereby, the carbonate cement precipitated mostly under eodiagenetic conditions near the sediment/water interface (<~3 m in depth). The distribution of these structures is confined to parasequence-bounding flooding surfaces (generally expressed as transgressive surfaces of erosion). Notably, sedimentological, ichnological and paragenetic data can be related to stratigraphic evolution such that geochemical and textural evidence is distinctly associated with (1) early cementation of the host sandstone during highstands of relative sea level, (2) the formation of firmgrounds during low relative sea level, (3) the development of a Glossifungites-demarcated discontinuity during initial relative sea-level rise, and (4) continued cementation with rising relative sea level. This was followed by burial diagenesis, evidence for which is derived from petrographic and isotopic data.  相似文献   

20.
Analyses of major element and volatile components of amphiboles from Vulcan's Throne, a Recent volcano on the north rim of the Grand Canyon, Arizona, USA, have been performed by using the electron microprobe and high temperature mass spectrometry. The amphiboles occur as megacrysts, as oikocrysts in peridotite and pyroxenite xenoliths, in amphibole-rich selvages on lherzolite xenoliths, and as grains in hornblendite xenoliths. Total volatiles range from 1.27 to 1.75 wt.%. In all samples, H2O is the principal volatile species. Lesser amounts of structurally bound fluorine, chlorine, and oxygen were also released. The amphiboles studied are hydroxyl-deficient. The O(3) site is probably partially occupied by O2?, which was detected as O2 during degassing of the amphibole. Ti shows a strong positive correlation with the amount of hydroxyl deficiency in the amphiboles except for one oxidized sample. Thus, Ti probably is significant in charge balancing the substitution of O2? for OH? and the substitution probably occurred during crystallization rather than by dehydrogenation. Small amounts of both oxidized and reduced carbon and sulfur-bearing volatile species (e.g., CO2, CO, CH4, SO2, H2S) were detected in all samples. The observation of reduced carbon species supports the hypothesis that the oxygen fugacity of at least portions of the upper mantle is probably less than the quartz-fayalite-magnetite buffer.  相似文献   

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