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1.
Analysis of carbon and oxygen isotopic compositions of large benthic foraminifera tests (Marginopora vertebralis) that lived in the Great Australian Bight during the late Pleistocene, reveal that the tests are enriched by 1 to 3‰ in both 18O and 13C relative to modern specimens from the same region. The intolerance of M. vertebralis for cool waters negates lower ocean water temperature as an explanation for such high δ18O values. The oxygen isotopic compositions are thus interpreted to reflect tests secreted in hypersaline waters of up to 56 ppt salinity, concentrated from seawater by evaporation. M. vertebralis thrives today in waters of similar salinity at Shark Bay, Western Australia. The Pleistocene sedimentary assemblage supports an interpretation that environments broadly similar to those in outer modern-day Shark Bay were wide spread across the Great Australian Bight during portions of marine isotope stages 2, 3 and 4. The high δ13C values of the Pleistocene M. vertebralis are interpreted to reflect enhanced photosynthetic activity that depletes dissolved carbonate in 12C in such shallow, saline settings. These hypersaline environments formed during periods of lower sea-level when shallow-waters (< 20 m depth) extended from the shoreline over ~ 100 km across what is currently a relatively deep shelf. This study indicates that shelf bathymetry was a critical determinant of past environments of deposition across the Great Australian Bight. 相似文献
2.
《Gondwana Research》2014,26(4):1357-1368
Oceanic Anoxic Event 2 (OAE 2) during the Cenomanian–Turonian (C/T) transition caused stepwise marine extinctions. Using organic compounds, stable carbon and oxygen isotopes, and foraminifera from three depth-transect sections in northern Spain, this study revealed repeated anoxic/euxinic events coinciding with warming and stepwise extinctions of planktonic and/or benthic foraminifera within intermediate to surface waters in the proto-North Atlantic during the C/T transition. Those short-duration euxinic events occurred four times: at 93.95 Ma, marked by the extinction of Rotalipora greenhornensis; at 93.90 Ma, marked by the extinction of Rotalipora cushmani; at the mid-time maximum of the plateau of the δ13C of carbonates (93.70 Ma); and at the time of the C/T boundary (93.55 Ma). Furthermore, the main benthic foraminiferal extinctions occurred during the first and second euxinic events in the upper slope, during the second and third euxinic events in the outer to middle shelf, and during the third and fourth events in the middle shelf. The main euxinic events in each section also showed a progression to the shallow shelf. The main anoxia–extinction events occurred in the upper slope and outer shelf then moved to the middle shelf. The shallowest section had relatively weak anoxia and a proportionally low extinction rate. These new findings indicate that foraminiferal extinctions started from the intermediate water and the continental slope and then moved to the continental shelf. This was the result of the repeated progression of euxinic–anoxic water from the upper slope to the middle shelf on the eastern continental margin of the proto-North Atlantic four times during a 400 kyr period, to the end of the Cenomanian. 相似文献
3.
《Sedimentary Geology》2006,183(1-2):15-30
Carbonate concretions in the Miocene sedimentary rocks of the Yeonil Group in the Pohang Basin (Korea) were investigated in terms of stable oxygen and carbon isotope composition to delineate the origin and associated diagenetic environment for their formation. Carbonate concretions are widely distributed in all the sedimentary rocks in the Pohang Basin, showing that the calcitic concretions are preserved within the mass-flow deposits and the dolomitic ones mostly in the hemipelagic siliceous rocks (diatomites). Concretions can be classified into four different types, on the basis of the stable isotopic signatures, each of which represents its own geochemical range.Type I concretions are calcitic and are composed of micrite to microspar. They occur in the conglomerates and sandstones which were deposited by mass flows (debris flow to turbidity current). It shows relatively lower δ18O (− 14.0 to − 9.3‰) and δ13C (− 19.6 to − 8.4‰) values. These concretions grew in a sulfate reducing zone under the influence of residual ambient seawater which had been significantly modified by volcanogenic sediments. Type II concretions are also calcitic, composed mostly of micrite with minor microspar and found in the sandstones. These concretions are characterized by relatively high δ18O (+ 1.8 to + 2.4‰) and variable δ13C (− 17.3 to − 0.4‰) values. These isotopic signatures reflect that Type II concretions formed from just beneath the sediment/water interface down to the sulfate reducing zone through the early stage of methanogenesis. Type III concretions are also calcitic, and composed largely of micrite with a minor contribution of microspar. They are observed in hemipelagic mudrocks which were deposited under the influence of mass flows. They are characterized by intermediate to high δ18O (− 4.6 to + 1.6‰) and high δ13C (− 1.3 to + 8.8‰) values. These concretions grew in a methanogenic zone by residual ambient seawater and/or seawater slightly modified by reaction with volcanogenic sediments. Type IV concretions are dolomite with calcite inclusion, and occur in hemipelagic siliceous rocks. These concretions are mostly composed of micrite and characterized by variable δ18O (− 9.1 to + 0.7‰) and high δ13C (+ 3.1 to + 17.9‰) values, suggesting formation in the methanogenic zone, although the residual ambient seawater is slightly modified by volcanogenic sediments.The same type of the concretions is widely distributed throughout the basin and always shows its own distinctive stable isotopic signature. This means that the formation of the given type depends upon the lithology and composition of host sediments that are closely related to the depositional process of the fan-delta systems regardless of their localities. Further, the different types of concretions are also found at the different, but closely spaced stratigraphic levels in the same locality, displaying the distinctive diagenetic conditions for each type. Such preservation of the unique diagenetic signatures in individual type of concretion suggests that the concretions formed in a completely closed diagenetic system. Therefore, caution should be made to simplify and generalize the diagenetic condition for the formation of any concretions in a large sedimentary basin. 相似文献
4.
Although oil cracking has been documented as one of the important sources of gas in many overmature marine sedimentary basins, the chemical and carbon isotopic signatures of gases of this origin are still open to question. In this study a Cambrian crude oil from the central Tarim basin, along with its main separated fractions (saturates, aromatics and asphaltenes), were pyrolyzed in sealed gold tubes to investigate how generated gases vary in chemical and carbon isotopic composition and how this variation would influence the genetic interpretation of oil cracking gas. The results indicate that the gases from cracking of aromatics and asphaltenes are much drier and more enriched in 13C than the gases from the cracking of saturates and crude oil at the same level of thermal maturity. In the experimental run of 20 °C/h, the dryness index of the gases (defined as the volume percentage of C1 in C1–5) from the cracking of saturates ranges from 26.2–90.6% with the methane carbon isotope change ranging from −54.8‰ to −35.5‰, whereas the dryness index is never lower than 60.6% for the gases from the cracking of aromatics with methane carbon isotope ranging from −39.9‰ to −32.2‰. Correspondingly, experimental data for the four samples plot in different areas in diagrams designed to distinguish oil cracking gas from kerogen cracking gas, such as ln(C2/C3) vs. δ13C2–δ13C3 and δ13C1 vs. δ13C2–δ13C3, indicating compositional variability of crude oil could assert an important influence in these diagrams. Therefore it is prudent to bring other geological constraints into consideration to avoid misinterpretation.The kinetic parameters for the bulk generation of C1–5 gas and the methane carbon isotope fractionation extrapolated to geological conditions of 2 °C/Ma and an initial temperature of 50 °C show that the temperatures of C1–5 gas generation from the aromatics and asphaltenes are lower than those from the saturates and crude oil due to their lower activation energies and frequency factors. Generation of C1–5 gases from the aromatics is modeled to be initiated about 122 °C whereas the initiation temperature for the saturates sample is 176 °C. Below 189 °C (EasyRo = 1.8%), the yields of C1–5 gases follow the order: aromatics > asphaltenes > crude oil > saturates. At similar thermal maturity levels, the methane carbon isotopic compositions are significantly different for the four samples, with an order of 13C enrichment: aromatics > asphaltenes > crude oil > saturates, however the difference in methane carbon isotopes becomes smaller with increasing temperature. This indicates that methane carbon isotopic values can be significantly different for gases cracked from oils that are compositionally diverse, especially in the early stage of methane generation. 相似文献
5.
Western tropical Pacific sea surface temperatures and Pacific Deep Water temperatures during Marine Isotope Stage 3 have been reconstructed from the δ18O and Mg/Ca of planktonic and benthic foraminifera from Marion Dufresne core MD98-2181. This 36 m marine core was collected at 6.3°N from a water depth of 2114 m. With sediment accumulation rates of up to 80 cm/ky, it provides a decadally resolved history of ocean variability during the Last Glacial period. Surface temperatures and salinities at this site varied in close association with millennial-scale atmospheric temperature swings at high northern latitudes as reflected in the GISP2 ice core. At times of colder atmospheric temperatures over Greenland, the western Pacific was more saline and summer season SSTs were ～2 °C colder. These millennial-scale changes within the tropics are attributed to a southward displacement of the summer season ITCZ in response to steeper meridional temperature gradients within the Pacific. The benthic δ18O record from MD98-2181 documents upper Pacific Deep Water temperature and salinity variability. Benthic δ18O variations of 0.3–0.5‰ during MIS 3 indicate deep waters within the Pacific were varying by ～1–1.5 °C, with the possibility that some of the variability was due to changing salinity and minor glacial–eustatic changes. The observed deep-water variability correlates to changes in Antarctic surface temperatures and thus reflects changes in Southern Ocean temperatures at the site of Pacific Deep Water formation. The combined planktonic and benthic records from MD98-2181 thus provide a northern and southern hemispheric climate record of anti-phased variability during MIS 3 as has been inferred previously from ice core records. Furthermore, the deep sea temperature excursions appear to have led millennial variations in atmospheric CO2 as recorded in the EDML ice core by ～1 kyr. 相似文献
6.
《Applied Geochemistry》2005,20(8):1496-1517
Chloride concentrations were as high as 230 mg/L in water from the surface discharge of long-screened production wells in Pleasant Valley, Calif., about 100 km NW of Los Angeles. Wells with the higher Cl− concentrations were near faults that bound the valley. Depending on well construction, high-Cl−water from different sources may enter a well at different depths. For example, Cl− concentration in the upper part of some wells completed in overlying aquifers influenced by irrigation return were as high as 220 mg/L, and Cl− concentrations in water sampled within wells at depths greater than 450 m were as high as 500 mg/L. These high-Cl− waters mix within the well during pumping and produce the water sampled at the surface discharge. Changes in the major ion, minor ion, trace element, and δ34S and δ13C isotopic composition of water in wells with depth were consistent with changes resulting from SO4 reduction, precipitation of calcite, and cation exchange. The chemical and isotopic composition of high-Cl− water from deep wells trends towards the composition of oil-field production water from the study area. Chloride concentrations in oil-field production water present at depths 150 m beneath freshwater aquifers were 2200 mg/L, and Cl− concentrations in underlying marine rock were as high as 4400 mg/L. High-Cl− concentrations in water from deeper parts of wells were associated with dissolved organic C composed primarily of hydrophobic neutral compounds believed to be similar to those associated with petroleum in underlying deposits. These compounds would not be apparent using traditional sampling techniques and would not be detected using analytical methods intended to measure contamination. 相似文献
7.
《Applied Geochemistry》2005,20(1):23-39
Hydrothermal alteration at Los Azufres geothermal field is mostly propylitic with a progressive dehydration with depth and temperature increase. Argillic and advanced argillic zones overlie the propylitic zone owing to the activity of gases in the system. The deepest fluid inclusions (proto-fluid) are liquid-rich with low salinity, with NaCl dominant fluid type and ice melting temperatures (Tmi) near zero (0 °C), and salinities of 0.8 wt% NaCl equivalent. The homogenization temperature (Th) = 325 ± 5 °C. The boiling zone shows Th = ±300 °C and apparent salinities between 1 and 4.9 wt% NaCl equivalent, implying a vaporization process and a very important participation of non-condensable gases (NCGs), mostly CO2. Positive clathrate melting temperatures (fusion) with Th = 150 °C are observed in the upper part of the geothermal reservoir (from 0 to 700 m depth). These could well be the evidence of a high gas concentration. The current water produced at the geothermal wells is NaCl rich (geothermal brine) and is fully equilibrated with the host rock at temperatures between T = 300 and 340 °C. The hot spring waters are acid-sulfate, indicating that they are derived from meteoric water heated by geothermal steam. The NCGs related to the steam dominant zone are composed mostly of CO2 (80–98% of all the gases). The gases represent between 2 and 9 wt% of the total mass of the fluid of the reservoir.The authors interpret the evolution of this system as deep liquid water boiling when ascending through fractures connected to the surface. Boiling is caused by a drop of pressure, which favors an increase in the steam phase within the brine ascending towards the surface. During this ascent, the fluid becomes steam-dominant in the shallowest zone, and mixes with meteoric water in perched aquifers. Stable isotope compositions (δ18O–δD) of the geothermal brine indicate mixing between meteoric water and a minor magmatic component. The enrichment in δ18O is due to the rock–water interaction at relatively high temperatures. δ13C stable isotope data show a magmatic source with a minor meteoric contribution for CO2. The initial isotopic value δ34SRES = −2.3‰, which implies a magmatic source. More negative values are observed for shallow pyrite and range from δ34S (FeS2) = −4‰ to −4.9‰, indicating boiling. The same fractionation tendencies are observed for fluids in the reservoir from results for δ18O. 相似文献
8.
We investigate the helium, carbon and oxygen–hydrogen isotopic systematics and CO2/3He ratios of 8 water and 6 gas samples collected from 12 geothermal fields in western Anatolia (Turkey). 3He/4He ratios of the samples (R) normalized to the atmospheric 3He/4He ratio (RA = 1.39 × 10? 6) range from 0.27 to 1.67 and are significantly higher than the crustal production value of 0.05. Fluids with relatively high R / RA values are generally found in areas of significant heat potential (K?z?ldere and Tuzla fields). CO2/3He ratios of the samples, ranging from 1.6 × 109 to 2.3 × 1014, display significant variation and are mostly higher than values typical of an upper mantle source (2 × 109). The δ13C (CO2) and δ13C (CH4) values of all fluids vary from ? 8.04 to + 0.35‰ and ? 25.80 to ? 23.92‰ (vs. PDB), respectively. Stable isotope values (δ18O–δD) of the geothermal waters are conformable with the Mediterranean Meteoric Water Line and indicate a meteoric origin. The temperatures calculated by gas geothermometry are significantly higher than estimates from chemical geothermometers, implying that either equilibrium has not been attained for the isotope exchange reaction or that isotopic equilibration was disturbed due to gas additions en route to the surface.Evaluation of He–CO2 abundances indicates that hydrothermal degassing and calcite precipitation (controlled probably by adiabatic cooling due to degassing) significantly fractionate the elemental ratio (CO2/3He) in geothermal waters. Such processes do not affect gas phase samples to anywhere near the same extent. For the gas samples, mixing between mantle and various crustal sources appears to be the main control on the observed He–C systematics: however, crustal inputs dominate the CO2 inventory. Considering that limestone is the main source of carbon (～ 70 to 97% of the total carbon inventory), the carbon flux from the crust is found to be at least 20 times that from the mantle. As to the He-inventory, the mantle-derived component is found to vary up to 21% of the total He content and is probably transferred to the crust by fluids degassed from deep mantle melts generated in association with the elevated geotherm and adiabatic melting accompanying current extension. The range of 3He/enthalpy ratios (0.000032 to 0.19 × 10? 12 cm3 STP/J) of fluids in western Anatolia is consistent with the release of both helium and heat from contemporary additions of mantle-derived magmas to the crust. The deep faults appear to have facilitated the deep circulation of the fluids and the transport of mantle volatiles and heat to the surface. 相似文献
9.
Calcite veins with fluid and solid bitumen inclusions have been discovered in the south-western shoulder of the Dead Sea rift within the Masada-Zohar block, where hydrocarbons exist in small commercial gas fields and non-commercial fields of heavy and light oils. The gas–liquid inclusions in calcite are dominated either by methane or CO2, and aqueous inclusions sometimes bear minor dissolved hydrocarbons. The enclosed flake-like solid bitumen matter is a residue of degraded oil, which may be interpreted as “dead carbon”. About 2/3 of this matter is soot-like amorphous carbon and 1/3 consists of n-C8C18 carboxylic acids and traces of n-alkanes, light dicarboxylic acids, and higher molecular weight (>C20) branched and/or cyclic carboxylic acids. Both bitumen and the host calcites show genetic relationship with mature Maastrichtian chalky source rocks (MCSRs) evident in isotopic compositions (δ13C, δ34S, and δ18O) and in REE + Y patterns. The bitumen precursor may have been heavy sulfur-rich oil which was generated during the burial compaction of the MCSR strata within the subsided blocks of the Dead Sea graben. The δ18O and δ13C values and REE + Y signatures in calcites indicate mixing of deep buried fluids equilibrated with post-mature sediments and meteoric waters. The temperatures of fluid generation according to Mg–Li-geothermometer data range from 55 °С to 90 °С corresponding to the 2.5–4.0 km depths, and largely overlap with the oil window range (60–90 °С) in the Dead Sea rift (Hunt, 1996; Gvirtzman and Stanislavsky, 2000; Buryakovsky et al., 2005). The bitumen-rich vein calcites originated in the course of Late Cenozoic rifting and related deformation, when tectonic stress triggers damaged small hydrocarbon reservoirs in the area, produced pathways, and caused hydrocarbon-bearing fluids to rise to the subsurface; the fluids filled open fractures and crystallized to calcite with entrapped bitumen. The reported results are in good agreement with the existing views of maturation, migration, and accumulation of hydrocarbons, as well as basin fluid transport processes in the Dead Sea area. 相似文献
10.
Interpretation of the Thomson Orogen and its context within the Tasmanides of eastern Australia is hampered by vast areas of deep sedimentary cover which also mask potential relationships between central and eastern Australia. Within covered areas, basement drill cores offer the only direct geological information. This study presents new detrital zircon isotopic data from these drill cores and poorly understood outcropping units to provide new age and provenance information for sedimentary rocks from the Thomson Orogen. Two distinct detrital zircon signatures are revealed. One is dominated by Grenvillian-aged (1300–900 Ma) zircons with a significant peak at ~ 1180 Ma and lesser peak at ~ 1070 Ma. These age peaks, along with Lu–Hf isotopic compositions (median εHf(t) = + 1.5), dominantly mantle-like δ18O values (median = 5.53‰) and model ages of ~ 1.89 Ga, support a Musgrave Province (central Australia) source. The dominance of Grenvillian-aged material additionally points to deposition during the Petermann Orogeny (570–530 Ma) when the Musgrave Province was uplifted, shedding abundant material to the Centralian Superbasin. Comparable age spectra suggest that parts of the Thomson Orogen were connected to the Centralian Superbasin during this period. We use the term ‘Syn-Petermann’ to describe this signature which is observed in two drill cores adjacent to the North Australian Craton and scattered units in the outcropping Thomson Orogen. The second signature marks a significant provenance shift and is remarkably consistent throughout the Thomson Orogen. Age spectra exhibit dominant peaks at 600–560 Ma, lesser 1300–900 Ma populations and maximum depositional ages of ~ 495 Ma. This pattern is termed the ‘Pacific Gondwana’ detrital zircon signature and is recognised throughout eastern Australia, Antarctica and central Australia. Lu–Hf isotope data for Thomson Orogen rocks with this signature are highly variable with εHf(t) values between ‐ 49 and + 10 and dominantly supracrustal δ18O values suggesting input from different and more diverse source regions relative to those exhibiting the Syn-Petermann signature. 相似文献
11.
The Hukeng tungsten deposit, located in the Wugongshan area in central part of Jiangxi province, South China, is a large-scale quartz-vein wolframite deposit. It is hosted in the Hukeng granitic intrusion. Based on the mineral assemblage and crosscutting relationship of the veins, three mineralization stages are identified, including: (1) quartz–wolframite stage, (2) quartz–fluorite–wolframite stage, and (3) quartz–pyrite–sphalerite–wolframite stage.The homogenization temperatures of fluid inclusions in vein quartz vary from 220 to 320 °C, and the salinities are from 0 to 10 wt.% NaCl equiv.; corresponding densities range from 0.7 to 1 g/cm3. These features indicated that the ore-forming fluids in the Hukeng tungsten deposit have medium temperature, low density and low salinity.The δ18OSMOW values of quartz range from 10.8‰ to 14.4‰, with corresponding δ18Ofluid values of 3.7‰ to 7.7‰, and δD values of fluid inclusions of between ? 70‰ and ? 55‰. The combined isotopic data indicate that the ore-forming fluids of the Hukeng tungsten deposit were mainly derived from magmatic water, with some minor input from meteoric water.We have carried out molybdenite Re–Os and muscovite 40Ar/39Ar dating to constrain the timing of mineralization. Re–Os dating of six molybdenite samples yielded model ages ranging from 149.1 ± 2.0 to 150.7 ± 3.7 Ma, with an average of 150.0 Ma. The Re–Os analyses give a well-defined 187Re/187Os isochron with an age of 150.2 ± 2.2 Ma (MSWD = 0.60). Hydrothermal muscovite yields a plateau 40Ar/39Ar age of 147.2 ± 1.4 Ma. 40Ar/39Ar age is in good agreement with the Re–Os age. These ages show that the timing of tungsten mineralization occurred at about 150 Ma. Our new data, when combined with published geochronological results from the other major deposits in this region, suggest that widespread W mineralization occurred in the Late Jurassic throughout South China. 相似文献
12.
《Quaternary Science Reviews》2007,26(5-6):808-827
During the Late Pliocene–Middle Pleistocene, 56 species and 15 genera of elongate, cylindrical benthic foraminifera disappeared from the deep sea in the South China Sea (ODP Sites 1143 and 1146) as part of the last global extinction in the deep sea. This extinction group (Ext. Gp) exhibited a pulsed decline in abundance and species richness mostly during glacials, and often associated with periods of expansion of polar ice that resulted from increased cooling of the Earth's climate since ∼2.5 Ma, particularly during the Mid-Pleistocene Climate Transition (MPT, 1.2–0.6 Ma). We infer that the Ext. Gp decline in abundance and disappearance was a result of the increased glacial cooling and consequent increased ventilation of the deep-sea water masses. The detailed record of withdrawal of the Ext. Gp differs between the two sites, with far more disappearances occurring prior to the MPT in the deeper Site 1143 (2772 m) than in the shallower Site 1146 (2092 m). The Late Pliocene and Early Pleistocene declines in deeper parts of the South China Sea (Site 1143) may have resulted from enhanced glacial production of deep, southern-sourced water passing over the sill into the basin from the North-west Pacific. During the MPT however, the Ext. Gp declines and disappearances were of similar timing and magnitude in both sites, implying that both were influenced by the same deep-water mass during glacials at this time. This could have been North Pacific Deep Water, which many workers infer was formed in the northern Pacific during the last glacial, and may have begun forming during MPT glacials, in association with the progressively enhanced cooling of the Northern Hemisphere. 相似文献
13.
The potential to provide environmental proxies using stable carbon isotopes from modern and archaeological charcoal is explored. Experiments on modern Podocarpus (Yellowwoods) show that δ13C values of stems, branches and charcoal preserve proxy environmental conditions, including rainfall, humidity and temperature. An additional experiment showed that combustion temperature affects the carbon isotope signature of charcoal. Burning at 450 °C to 500 °C depletes δ13C values with respect to the original wood, but the charcoal retains the seasonal and inter-annual isotopic trends recorded during the growth of the tree.The δ13C of Podocarpus charcoal from three levels from the Middle Stone Age site of Sibudu Cave, KwaZulu-Natal, South Africa, was compared with modern analogues from two different environments, Seaton Park (KwaZulu-Natal) and the Baviaans Kloof (Eastern Cape). Other environmental proxies from levels dated from > 70 ka and ~ 48 ka, show that environmental conditions changed from warmer and wetter to colder and drier and finally becoming warmer and drier. The isotope data is consistent with this reconstruction. The results from this series of experiments indicate that it is possible to obtain meaningful palaeoenvironmental information from δ13C values of archaeological charcoal. 相似文献
14.
《Comptes Rendus Geoscience》2015,347(1):24-34
Oxygen isotope signatures of ruby and sapphire megacrysts, combined with trace-element analysis, from the Mbuji-Mayi kimberlite, Democratic Republic of Congo, and the Changle alkali basalt, China, provide clues to specify their origin in the deep Earth. At Mbuji-Mayi, pink sapphires have δ18O values in the range 4.3 to 5.4‰ (N = 10) with a mean of 4.9 ± 0.4‰, and rubies from 5.5 to 5.6‰ (N = 3). The Ga/Mg ratio of pink sapphires is between 1.9 and 3.9, and in rubies, between 0.6 and 2.6. The blue or yellow sapphires from Changle have δ18O values from 4.6 to 5.2 ‰, with a mean of 4.9 ± 0.2‰ (N = 9). The Ga/Mg ratio is between 5.7 and 11.3. The homogenous isotopic composition of ruby suggests a derivation from upper mantle xenoliths (garnet lherzolite, pyroxenite) or metagabbros and/or lower crustal garnet clinopyroxenite eclogite-type xenoliths included in kimberlites. Data from the pink sapphires from Mbuji-Mayi suggest a mantle origin, but different probable protoliths: either subducted oceanic protolith transformed into eclogite with δ18O values buffered to the mantle value, or clinopyroxenite protoliths in peridotite. The Changle sapphires have a mantle O-isotope signature. They probably formed in syenitic magmas produced by low degree partial melting of a spinel lherzolite source. The kimberlite and the alkali basalt acted as gem conveyors from the upper mantle up to the surface. 相似文献
15.
《Applied Geochemistry》2005,20(11):2017-2037
The Tertiary Thrace Basin located in NW Turkey comprises 9 km of clastic-sedimentary column ranging in age from Early Eocene to Recent in age. Fifteen natural gas and 10 associated condensate samples collected from the 11 different gas fields along the NW–SE extending zone of the northern portion of the basin were evaluated on the basis of their chemical and individual C isotopic compositions. For the purpose of the study, the genesis of CH4, thermogenic C2+ gases, and associated condensates were evaluated separately.Methane appears to have 3 origins: Group-1 CH4 is bacteriogenic (Calculated δ13CC1–C = −61.48‰; Silivri Field) and found in Oligocene reservoirs and mixed with the thermogenic Group-2 CH4. They probably formed in the Upper Oligocene coal and shales deposited in a marshy-swamp environment of fluvio-deltaic settings. Group-2 (δ13CC1–C = −35.80‰; Hamitabat Field) and Group-3 (δ13C1–C = −49.10‰; Değirmenköy Field) methanes are thermogenic and share the same origin with the Group-2 and Group-3 C2+ gases. The Group-2 C2+ gases include 63% of the gas fields. They are produced from both Eocene (overwhelmingly) and Oligocene reservoirs. These gases were almost certainly generated from isotopically heavy terrestrial kerogen (δ13C = −21‰) present in the Eocene deltaic Hamitabat shales. The Group-3 C2+ gases, produced from one field, were generated from isotopically light marine kerogen (δ13C = −29‰). Lower Oligoce ne Mezardere shales deposited in pro-deltaic settings are believed to be the source of these gases.The bulk and individual n-alkane isotopic relationships between the rock extracts, gases, condensates and oils from the basin differentiated two Groups of condensates, which can be genetically linked to the Group-2 and -3 thermogenic C2+ gases. However, it is crucial to note that condensates do not necessarily correlate to their associated gases.Maturity assessments on the Group-1 and -2 thermogenic gases based on their estimated initial kerogen isotope values (δ13C = −21‰; −29‰) and on the biomarkers present in the associated condensates reveal that all the hydrocarbons including gases, condensates and oils are the products of primary cracking at the early mature st age (Req = 0.55–0.81%). It is demonstrated that the open-system source conditions required for such an early-mature hydrocarbon expulsion exist and are supported by fault systems of the basin. 相似文献
16.
This study provides 87Sr/86Sr, δ13C and δ18O data from the best-preserved limestone and dolomite of the Ediacaran carbonate-dominated Khorbusuonka Group of the Olenek Uplift, NE Siberian Craton, as well as detrital zircon geochronological data from both underlying and overlying sandstones. The Maastakh Formation is characterized by 87Sr/86Sr ratios of ca. 0.70822 and δ13C values between + 4.8 and + 6.0‰. 87Sr/86Sr ratios in limestones of the Khatyspyt Formation are fairly uniform, ranging from 0.70783 to 0.70806. The carbon isotopic composition slowly decreases from bottom (+ 3.7‰) to top (− 0.2‰) of section. The Sr isotopic composition of the Turkut Formation varies from 0.70824 to 0.70914, value of δ13C is about zero: − 0.7…+0.7 ‰. The youngest population of detrital zircons from Maastakh Formation indicates that these rocks were formed not later than 630 Ma. U–Pb detrital zircons data of Kessyusa Group has a single peak at about 543 Ma, which is almost identical to the earlier dating. Based on biostratigraphy and isotopic data, the Sr isotopic compositions from the Khatyspyt Formation (87Sr/86Sr = 0.70783–0.70806) represent the composition of seawater at 560–550 Ma. Such low values of 87Sr/86Sr ratio in Ediacaran water were probably caused by the quick opening of Iapetus Ocean. 相似文献
17.
《Comptes Rendus Geoscience》2018,350(8):476-486
In this study, the model H(i) = 109.6103 + C1 × F1(i) + C2 × F2(i) + … + C33 × F33(i) obtained from depth modelling based on 33 recent benthic foraminifer species distribution, has been applied to the fossil benthic foraminifers from the borehole GDEC-4-2 drilled at a water depth of 491 m, in the East-Corsica basin, covering the last 550,000 years. The obtained variations of the paleo-depths show a medium correlation with the oscillations of the relative sea level and also with the fluctuations of the oxygen isotopic ratio (δ18O G. bulloides and δ18O C. pachyderma–C. wuellerstorfi). This newly developed transfer function is accompanied by an error margin of ± 86 m, suggesting that this model will probably be more suitable for a time scale of the order of a million years where sea level variations are recorded with larger amplitudes. Without considering these problems related to amplitudes, it also turns out that the “eustatic” signal of the microfauna is accompanied by a “trophic” signal, which should not to be neglected, especially at a millennial scale time resolution. Thus, the application of this method would require taking into account the bottom trophic effects strongly controlling the distribution of benthic foraminifer assemblages. 相似文献
18.
A large number of Paleoproterozoic borate deposits are hosted by the lower units of a volcanic-sedimentary sequence in Liaoning Province, northeastern China, and are a major source of boron in China. The ore-bearing wall rocks in the deposits are serpentinized ultrabasic rocks and carbonates, with layered leptynites, leptites, amphibolites, and migmatites adjacent to the ore. Both the borate ores and country rocks contain tourmaline, although the country rocks have much lower abundances of the mineral. Based on in situ boron isotope measurements using laser ablation–multi-collector–inductively coupled plasma–mass spectrometry (LA–MC–ICP–MS), boron isotope data show that: (1) δ11B values of borate ores range from + 6.8‰ to + 13.9‰ (mean + 10.8‰); (2) tourmalines from the borate ores have δ11B values from + 9.5‰ to + 12.7‰; and (3) the wall rocks within the borate ores yield slightly lower δ11B values ranging from + 5.7‰ to + 7.6‰, and those outside the deposits from − 9.9‰ to − 5.9‰. Positive δ11B values in borates as well as in tourmalines inside the mining area indicate that boron in these Paleoproterozoic borate deposits was derived from marine evaporites. δ34SV-CDT (where V-CDT is Vienna Canyon Diablo Troilite) values of borate ores, serpentinized marbles, and anhydrites range from + 16.1‰ to + 24.7‰, whereas δ13CV-PDB (where V-PDB is Vienna Pee Dee Belemnite) values of marbles range from + 3.2‰ to + 5.9‰. These isotopic characteristics are interpreted to reflect formation in a marine evaporative environment. LA–MC–ICP–MS zircon weighted207Pb/206Pb ages of leptite and serpentinized olivine basalt from the hanging wall of the borate deposits are 2139 ± 13 Ma and 2130 ± 19 Ma, respectively. Therefore, the (~ 2.2 Ga) borate deposits may have originated from marine evaporative boron-bearing sediments, which were interbedded within bimodal volcanic rocks during the early stages of development of the Liaoji rift. 相似文献
19.
The Korba aquifer on the east coast of Cape Bon has been overexploited since the 1960s with a resultant reversal of the hydraulic gradient and a degradation of the quality due to seawater intrusion. In 2008 the authorities introduced integrated water resources planning based on a managed aquifer recharge with treated wastewater. Water quality monitoring was implemented in order to determine the different system components and trace the effectiveness of the artificial recharge. Groundwater samples taken from recharge control piezometers and surrounding farm wells were analyzed for their chemical contents, for their B isotopes, a proven tracer of groundwater salinization and domestic sewage, and their carbamazepine content, an anti-epileptic known to pass through wastewater treatment and so recognized as a pertinent tracer of wastewater contamination. The system equilibrium was permanently disturbed by the different temporal dynamics of continuous processes such as cation exchange, and by threshold processes linked to oxidation–reduction conditions. The B isotopic compositions significantly shifted back-and-forth due to mixing with end-members of various origin. Under the variable contribution of meteoric recharge, the Plio-Quaternary groundwater (δ11B of 35–40.6‰, a mean B concentration of 30 μmol/L, no carbamazepine, n = 7) was subject to seawater intrusion that induced a high δ11B level (δ11B of 41.5–48.0‰, a mean B concentration of 36 μmol/L, and n = 8). Fresh groundwater (δ11B of 19.89‰, B concentration of 2.8 μmol/L, no carbamazepine) was detected close to the recharge site and may represent the deep Miocene pole which feeds the upper Plio-Quaternary aquifer. The managed recharge water (δ11B of 10.67–13.8‰, n = 3) was brackish and of poor quality with a carbamazepine content showing a large short term variability with an average daily level of 328 ± 61 ng/L. A few piezometers in the vicinity of the recharge site gradually acquired a B isotopic composition close to the wastewater signature and showed an increasing carbamazepine content (from 20 to 910 ng/L). The combination of B isotopic signatures with B and carbamazepine contents is a useful tool to assess sources and mixing of treated wastewaters in groundwaters. Effluent quality needs to be greatly improved before injection to prevent further degradation of groundwater quality. 相似文献
20.
《Organic Geochemistry》2012,42(12):1269-1276
This study sought to characterize hydrogen isotopic fractionation during biosynthesis of leaf wax n-alkanes in succulent plants capable of crassulacean acid metabolism (CAM). The metabolic and physiological features of CAM represent crucial strategies for survival in hot and dry climates and have been hypothesized to impact hydrogen isotope fractionation. We measured the stable carbon and hydrogen isotopic compositions (δ13C and δD, respectively) of individual n-alkanes in 20 species of succulent plants from a global collection of the Huntington Botanical Gardens, San Marino, California. Greenhouse conditions and irrigation with water of constant δD value enabled determination of interspecies differences in net D/H fractionation between source water and leaf wax products. Carbon isotope ratios provide constraints on the extent of CAM vs. C3 photosynthesis and indicate a wide range of CAM use, with δ13C values ranging from −33.01‰ to −18.54‰ (C27–C33 n-alkanes) and −26.66‰ to −17.64‰ (bulk tissue). Despite the controlled growth environment, we observed ca. 90‰ interspecies range in δD values from −193‰ to −107‰. A positive correlation between δ13Cbulk and δDC31 values with R2 = 0.60 (δ13CC31 and δDC31 values with R2 = 0.41) implicates a metabolic isotope effect as the dominant cause of interspecies variation in the hydrogen isotopic composition of leaf wax n-alkanes in CAM-intermediate plants. 相似文献