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1.
The causes of the pronounced negative excursion in carbon-isotope values that was recorded during the Early Toarcian Oceanic Anoxic Event (T-OAE) are still under debate, particularly with regard to the local versus global pattern of the excursion, and the extent to which recorded signals are under a diagenetic control. In this study we employ a novel microseparation technique in order to investigate the isotopic and mineralogical characteristics of different size fractions of the carbonate content from a Toarcian section recovered from the Sancerre–Couy borehole, southern Paris Basin. Beyond the recognition of a ? 6‰ δ13C excursion in the bulk carbonate content, our data also demonstrate that biogenic particles (such as coccoliths) and inorganic grains precipitated as early diagenetic phases (including dolomite) both record the excursion with the same magnitude. Although several black shales occur through the Paris Basin Toarcian section, it is only that associated with the onset of the OAE that coincides with a large negative carbon-isotope excursion. Taken together these observations indicate that during this event, the entire water column was characterized by homogeneous carbon-isotope values; such a pattern is incompatible with the idea that the negative excursion was generated simply through the upwelling of bottom waters enriched in re-mineralized organic carbon (cf. “the Küspert model”), since this would have required a strong vertical gradient in the water column. Additionally, the Paris Basin data show that the decrease in carbonate δ13C values during the OAE occurred in several discrete steps (each of some ? 2‰), as has previously been found for organic carbon substrates in other European sections. The stepped nature of the isotopic profile, which is part of a stratigraphic signature previously ascribed to Milankovitch forcing, is compatible with regular pulsed input of light carbon into the whole atmosphere–ocean system from a climatically sensitive source such as gas hydrate, or from thermal methanogenesis of organic-rich sediments in the Karoo–Ferrar large igneous province. Contrasts in the amplitude of the negative carbon-isotope excursion on a regional scale remain an important unexplained aspect of the Toarcian record.  相似文献   

2.
During the Mesozoic (250–64 Ma) intervals of about 0.5 Myr were subject to severe environmental changes, including high sea-surface temperature and very low oxygen content of marine water. These Oceanic Anoxic Events, or OAEs, occurred simultaneously with profound disturbance to the carbon cycle. The carbon-isotope anomaly in the Early Jurassic that marks the Toarcian Oceanic Anoxic Event (T-OAE) at ~ 182 Ma is characterized in marine sections by a series of dramatic steps towards lighter values. Herein we present new carbon-isotope data from terrestrial organic matter (phytoclast separates), collected through a Late Pliensbachian–Middle Toarcian coastal and marginal marine succession in the Polish Basin, a setting where hinterland climate and sea-level change are well recorded. The results show that the shift to light carbon-isotope values in the woody organic matter, and therefore also in atmospheric carbon dioxide, similarly occurred in major steps. The steps are here correlated with those identified from marine organic matter, where they have previously been attributed to 100 kyr eccentricity forcing of climate. The results provide strong support for orbitally and climatically controlled release of isotopically light carbon from gas hydrates into the ocean–atmosphere system in a series of rapid bursts. Additionally, a link between the carbon-isotope steps and shoreline movements can be demonstrated. Individual peaks of the negative excursion are mostly associated with facies indicative of sea-level rise (flooding surfaces). However, at the same time inferred higher atmospheric carbon-dioxide content may be expected to have resulted in increased rainfall and temperature, leading to accelerated weathering and erosion, and consequently increased sediment supply, progradation and regression, causing some mismatches between isotope shifts and inferred sea-level changes. Enhanced abundance of megaspores derived from hydrophilic plant groups, and marked increase in kaolinite, are coincident with the overall development of the negative isotope excursion. The combined data suggest that each 100-kyr cycle in carbon-isotope values was characterized by increasingly severe palaeoclimatic change, culminating in extremely hot and humid conditions co-incident with the peak of the final most negative carbon-isotope excursion. The chemostratigraphic correlation allows very precise dating of the Late Pliensbachian–Middle Toarcian coastal and marginal marine sedimentary succession in the Polish Basin.  相似文献   

3.
The Ca isotope compositions of 37 late Mesozoic skeletal carbonates, belemnites and brachiopods, from the Tethyan realm were analyzed by thermal (TIMS) and plasma (MC-ICP-MS) ionization mass spectrometry. A poor correlation between δ44/40Ca and δ18O values of belemnites suggests only a weak temperature dependency for the Ca isotope composition of belemnites, likely less than 0.02‰/°C. The δ44/40Ca record of belemnites was therefore used to reconstruct the Ca isotope composition of paleo-seawater (δ44/40CaSW), based on an experimentally determined fractionation factor between seawater Ca and belemnite calcite (αCC–SW) of ∼ 0.9986. The inferred δ44/40CaSW record, with an average stratigraphic resolution of 1 Ma, shows systematic temporal variation of ∼ 0.5‰ with the Middle/Late Jurassic (∼ 154 Ma) minimum of ∼ 1.4‰ and a subsequent general increase to the Early Cretaceous (∼ 124 Ma) maximum of ∼ 1.9‰. The global nature of the δ44/40CaSW record is supported by identical Ca isotope compositions of coeval (Kimmeridgian) belemnites collected from two distinct paleogeographic regions, the southern (New Zealand) and northern (Germany) margin of the Tethys Ocean. The observed late Mesozoic δ44/40CaSW record was simulated using a simple Ca isotope mass balance model, and the results indicate that the variation in δ44/40CaSW record can be explained by changes in oceanic input fluxes of Ca that were independent of the carbonate ion fluxes, such as the hydrothermal Ca flux or the release of Ca to the oceans via dolomitization of marine carbonates.  相似文献   

4.
A long-standing question in Paleogene climate concerns the frequency and mechanism of transient greenhouse gas-driven climate shifts (hyperthermals). The discovery of the greenhouse gas-driven Paleocene–Eocene Thermal Maximum (PETM; ～ 55 Ma) has spawned a search for analogous events in other parts of the Paleogene record. On the basis of high-resolution bulk sediment and foraminiferal stable isotope analyses performed on three lower Danian sections of the Atlantic Ocean, we report the discovery of a possible greenhouse gas-driven climatic event in the earliest Paleogene. This event – that we term the Dan-C2 event – is characterized by a conspicuous double negative excursion in δ13C and δ18O, associated with a double spike in increased clay content and decreased carbonate content. This suggests a double period of transient greenhouse gas-driven warming and dissolution of carbonates on the seafloor analogous to the PETM in the early Paleocene at ～ 65.2 Ma. However, the shape of the two negative carbon isotope excursions that make up the Dan-C2 event is different from the PETM carbon isotope profile. In the Dan-C2 event, these excursions are fairly symmetrical and each persisted for about ～ 40 ky and are separated by a short plateau that brings the combined duration to ～ 100 ky, suggesting a possible orbital control on the event. Because of the absence of a long recovery phase, we interpret the Dan-C2 event to have been associated with a redistribution of carbon that was already in the biosphere. The Dan-C2 event and other early Paleogene hyperthermals such as the short-lived early Eocene ELMO event may reflect amplification of a regular cycle in the size and productivity of the marine biosphere and the balance between burial of organic and carbonate carbon.  相似文献   

5.
《Continental Shelf Research》2006,26(17-18):2241-2259
The Amazon River spawns a vast mobile mudbelt extending ∼1600 km from the equator to the Orinoco delta. Deposits along the Amazon–Guianas coastline are characterized by some of the highest Corg remineralization rates reported for estuarine, deltaic, or shelf deposits, however, paradoxically, except where stabilized by mangroves or intertidal algal mats, they are usually suboxic and nonsulfidic. A combination of tides, wind-driven waves, and coastal currents forms massive fluid muds and mobile surface sediment layers ∼0.5–2 m thick which are dynamically refluxed and frequently reoxidized. Overall, the seabed functions as a periodically mixed batch reactor, efficiently remineralizing organic matter in a gigantic sedimentary incinerator of global importance. Amazon River material entering the head of this dynamic dispersal system carries an initial terrestrial sedimentary Corg loading of ∼ 0.7 mg C m−2 particle surface area. Total Corg loading is lowered to ∼ 0.2 mg C m−2 in the proximal delta topset, ∼60–70% of which remains of terrestrial origin. Loading decreases further to 0.12–0.14 mg C m−2 (∼60% terrestrial) in mudbanks ∼600 km downdrift along French Guiana, values comparable to those found in the oligotrophic deepsea. DOC/ΣCO2 ratios in pore waters of French Guiana mudbanks indicate that >90% of metabolized organic substrates are completely oxidized. Within the Amazon delta topset at the head of the dispersal system, both terrestrial and marine organic matter contribute substantially to early diagenetic remineralization, although reactive marine substrate dominates (∼60–70%). The conditional rate constant for terrestrial Corg in the delta topset is ∼0.2 a−1. As sedimentary Corg is depleted during transit, marine sources become virtually the exclusive substrate for remineralization except very near the mangrove shoreline. The δ13C and Δ14C values of pore water ΣCO2 in mudbanks demonstrate that the primary source of remineralized organic matter within ∼1 km of shore is a small quantity of bomb signature marine plankton (+80‰). Thus, fresh marine organic material is constantly entrained into mobile deposits and increasingly drives early diagenetic reactions along the transit path. Relatively refractory terrestrial Corg is lost more slowly but steadily during sedimentary refluxing and suboxic diagenesis. Amazon Fan deposits formed during low sea level stand largely bypassed this suboxic sedimentary incinerator and stored material with up to ∼3X the modern high stand inner shelf Corg load (Keil et al., 1997b. Proceedings of the Ocean Drilling Program, Scientific Results. Vol. 155. pp. 531–537). Sedimentary dynamics, including frequency and magnitude of remobilization, and the nature of dispersal systems are clearly key controls on diagenetic processes, biogeochemical cycling, and global C storage along the continental margins.  相似文献   

6.
We investigated the provenance of organic matter in the inner fjord area of northern Patagonia, Chile (～44–47°S), by studying the elemental (organic carbon, total nitrogen), isotopic (δ13C, δ15N), and biomarker (n-alkanoic acids from vascular plant waxes) composition of surface sediments as well as local marine and terrestrial organic matter. Average end-member values of N/C, δ13C, and δ15N from organic matter were 0.127±0.010, ?19.8±0.3‰, and 9.9±0.5‰ for autochthonous (marine) sources and 0.040±0.018, ?29.3±2.1‰, and 0.2±3.0‰ for allochthonous (terrestrial) sources. Using a mixing equation based on these two end-members, we calculated the relative contribution of marine and terrestrial organic carbon from the open ocean to the heads of fjords close to river outlets. The input of marine-derived organic carbon varied widely and accounted for 13–96% (average 61%) of the organic carbon pool of surface sediments. Integrated regional calculations for the inner fjord system of northern Patagonia covered in this study, which encompasses an area of ～4280 km2, suggest that carbon accumulation may account for between 2.3 and 7.8×104 ton C yr?1. This represents a storage capacity of marine-derived carbon between 1.8 and 6.2×104 ton yr?1, which corresponds to an assimilation rate of CO2 by marine photosynthesis between 0.06 and 0.23×106 ton yr?1. This rate suggests that the entire fjord system of Patagonia, which covers an area of ～240,000 km2, may represent a potentially important region for the global burial of marine organic matter and the sequestration of atmospheric CO2.  相似文献   

7.
To assess the environmental perturbation induced by the impact event that marks the Cretaceous–Tertiary (K–T) boundary, concentrations and isotopic compositions of bulk organic carbon were determined in sedimentary rocks that span the terrestrial K–T boundary at Dogie Creek, Montana, and Brownie Butte, Wyoming in the Western Interior of the United States. The boundary clays at both sites are not bounded by coals. Although coals consist mainly of organic matter derived from plant tissue, siliceous sedimentary rocks, such as shale and clay, may contain organic matter derived from microbiota as well as plants. Coals record δ13C values of plant-derived organic matter, reflecting the δ13C value of atmospheric CO2, whereas siliceous sedimentary rocks record the δ13C values of organic matter derived from plants and microbiota. The microbiota δ13C value reflects not only the δ13C value of atmospheric CO2, but also biological productivity. Therefore, the siliceous rocks from these sites yields information that differs from that obtained previously from coal beds.Across the freshwater K–T boundary at Brownie Butte, the δ13C values decrease by 2.6‰ (from − 26.15‰ below the boundary clay to − 28.78‰ above the boundary clay), similar to the trend in carbonate at marine K–T sites. This means that the organic δ13C values reflect the variation of δ13C of atmospheric CO2, which is in equilibrium with carbon isotopes at the ocean surface. Although a decrease in δ13C values is observed across the K–T boundary at Dogie Creek (from − 25.32‰ below the boundary clay to − 26.11‰ above the boundary clay), the degree of δ13C-decrease at Dogie Creek is smaller than that at Brownie Butte and that for marine carbonate.About 2‰ decrease in δ13C of atmospheric CO2 was expected from the δ13C variation of marine carbonate at the K–T boundary. This δ13C-decrease of atmospheric CO2 should affect the δ13C values of organic matter derived from plant tissue. As such a decrease in δ13C value was not observed at Dogie Creek, a process that compensates the δ13C-decrease of atmospheric CO2 should be involved. For example, the enhanced contribution of 13C-enriched organic matter derived from algae in a high-productivity environment could be responsible. The δ13C values of algal organic matter become higher than, and thus distinguishable from, those of plant organic matter in situations with high productivity, where dissolved HCO3− becomes an important carbon source, as well as dissolved CO2. As the δ13C-decrease of atmospheric CO2 reflected a reduction of marine productivity, the compensation of the δ13C decrease by the enhanced activity of the terrestrial microbiota means that the microbiota at freshwater environment recovered more rapidly than those in the marine environment.A distinct positive δ13C excursion of 2‰ in the K–T boundary clays is superimposed on the overall decreasing trend at Dogie Creek; this coincides with an increase in the content of organic carbon. We conclude that the K–T boundary clays include 13C-enriched organic matter derived from highly productive algae. Such a high biological productivity was induced by phenomena resulting from the K–T impact, such as nitrogen fertilization and/or eutrophication induced by enhanced sulfide formation. The high productivity recorded in the K–T boundary clays means that the freshwater environments (in contrast to marine environments) recovered rapidly enough to almost immediately (within 10 yr) respond to the impact-related environmental perturbations.  相似文献   

8.
The Early Jurassic Toarcian oceanic anoxic event (T-OAE) and concurrent negative carbon-isotope (δ13C) excursion have recently been attributed to either the release of methane (CH4) clathrates or thermogenic CH4 gas associated with the Karoo-Ferrar large igneous province (LIP) into coals and organic-rich shales. 12C-enriched thermogenic CH4 production associated with the Karoo-Ferrar would result in residual material being 12C-depleted nearer the intrusions. In this study, geochemical analyses (carbon isotopes, volatile matter (VM), vitrinite reflectance (Ro)) are reported for two coal transects associated with dykes intruding the No. 4L coal in the Highveld Coalfield, Karoo Basin, South Africa. VM decreases from over 35% to around 15% in one transect, and the second transect shows a less pronounced decrease (from > 25% to ~ 16%). Accompanying the decrease in VM content is an increase in Ro from background levels of around 0.7% to over 4% adjacent to the dyke; used as a palaeo-geothermometer, Ro values indicate background temperatures of ~ 100 °C increasing to > 300 °C close to the contact. Despite changes in VM and Ro, there are no significant changes in δ13C, certainly not of the magnitude that would be expected associated with large-scale thermogenic CH4 generation. These and other Gondwanan coals have low vitrinite and liptinite contents (components more prone to CH4 generation), in part explaining the modest decreases in VM adjacent to the dykes. This, combined with the relatively narrow metamorphic aureole surrounding the intrusions and the likelihood that at least some of the volatiles generated by the intrusion were trapped as coalbed CH4 or condensed as pyrolytic carbon, suggests only limited CH4 release. In addition, based on original estimates of moisture contents in these coals and the depth at time of intrusion (1,000–2,000 m) the dykes would have lost most of their energy heating and evaporating water, thus having very little remaining energy to generate thermogenic CH4.  相似文献   

9.
Silica alteration zones and cherts are a conspicuous feature of Archaean greenstone belts worldwide and provide evidence of extensive mobilisation of silica in the marine environment of the early Earth. In order to understand the process(es) of silicification we measured the silicon and oxygen isotope composition of sections of variably silicified basalts and overlying bedded cherts from the Theespruit, Hooggenoeg and Kromberg Formations of the Barberton Greenstone Belt, South Africa.The δ30Si and δ18O values of bulk rock increase with increasing amount of silicification from unsilicified basalts (?0.64‰ < δ30Si < ?0.01‰ and + 8.6‰ < δ18O < + 11.9‰) to silicified basalts (δ30Si and δ18O values as high as + 0.81‰ and + 15.6‰, respectively). Cherts generally have positive isotope ratios (+ 0.21‰ < δ30Si < + 1.05‰ and + 10.9 < δ18O < + 17.1), except two cherts, which have negative δ30Si values, but high δ18O (up to + 19.5‰).The pronounced positive correlations between δ30Si, δ18O and SiO2 imply that the isotope variation is driven by the silicification process which coevally introduced both 18O and 30Si into the basalts. The oxygen isotope variation in the basalts from about 8.6‰ to 15.6‰ is likely to represent temperature-dependent isotope fractionation during alteration. Our proposed model for the observed silicon isotope variation relies on a temperature-controlled basalt dissolution vs. silica deposition process.  相似文献   

10.
Li isotopic compositions of magmatic rocks have gained considerable attention recently as probes of mantle-scale processes. However, the concentrations and isotopic composition of Li in mantle minerals from mid-ocean ridges remain relatively unconstrained. This is largely because of the general presence of seawater alteration in abyssal peridotites. Lithium elemental and isotopic compositions for mineral separates of coexisting olivine, clinopyroxene, orthopyroxene and bulk rocks of serpentine-free Gakkel Ridge peridotites were investigated. Bulk rocks have Li contents of 1.6 to 2.7 ppm and δ7Li values of 3 to 5‰, which fall within the range of reported normal pristine “MORB mantle” values. Lithium concentrations vary in the order cpx (2.1–4.7 ppm) > opx (0.9–1.7 ppm) ≥ olivine (0.4–0.9 ppm), the opposite found in “equilibrated” mantle peridotite xenoliths (Seitz and Woodland, 2000). The Li isotopic compositions indicate a systematic mineral variation with δ7Liolivine (7.14‰–15.09‰) > δ7Liopx (1.81‰–3.66‰) > δ7Licpx (?2.43‰ ? ?0.39‰). The δ7Li values of cpx are negatively correlated with their Li concentrations with the lightest value for the most enriched cpx grains. There is a first order negative linear correlation between Δolivine–cpx (δ7Liolivine ? δ7Licpx) and ol/cpxD (Liolivine/Licpx).Numerical simulations indicate that the observed systematic inter-mineral variations of Li concentrations and isotopic compositions could be explained by a cooling driven diffusive redistribution between minerals in a closed system if there is a temperature dependent partitioning of Li between olivine and clinopyroxene. The studied Gakkel Ridge abyssal peridotites may alternatively have cooled under a variable cooling rate with a rapid cooling before the Li system was closed, which is less likely given the tectonic setting. Our calculations confirm that Li systematics in minerals, especially in coexisting mineral phases could potentially be used as a mantle geospeedometer, even for slowly cooled mantle rocks.  相似文献   

11.
Sampling and analyses methods for determining the stable isotopic compositions of Hg in an active volcanic system were tested and optimized at the volcanic complex of Vulcano (Aeolian Islands, Italy). Condensed gaseous fumarole Hg(fum)T, plume gaseous elemental Hg(g)0 and plume particulate Hg(p)II were obtained at fumaroles F0, F5, F11, and FA. The average total Hg emissions, based on HgT/SO2 in condensed fumarolic gases and plumes, range from 2.5 to 10.1 kg y? 1, in agreement with published values [Ferrara, R., Mazzolai, B., Lanzillotta, E., Nucaro, E., Pirrone, N., 2000. Volcanoes as emission sources of atmospheric mercury in the Mediterranean Basin. Sci. Total Environ. 259(1–3), 115–121; Aiuppa, A., Bagnato, E., Witt, M.L.I., Mather, T.A., Parello, F., Pyle, D.M., Martin, R.S., 2007. Real-time simultaneous detection of volcanic Hg and SO2 at La Fossa Crater, Vulcano (Aeolian Islands, Sicily). Geophys. Res. Lett. 34(L21307).]. Plume Hg(p)II increases with distance from the fumarole vent, at the expense of Hg(g)0 and indicates significant in-plume oxidation and condensation of fumarole Hg(fum)T.Relative to the NIST SRM 3133 Hg standard, the stable isotopic compositions of Hg are δ202Hg(fum)T = ? 0.74‰ ± 0.18 (2SD, n = 4) for condensed gaseous fumarole Hg(fum)T, δ202Hg(g)0 = ? 1.74‰ ± 0.36 (2SD, n = 1) for plume gaseous elemental Hg(g)0 at the F0 fumarole, and δ202Hg(p)II = ? 0.11‰ ± 0.18 (2SD, n = 4) for plume particulate Hg(p)II. The enrichment of Hg(p)II in the heavy isotopes and Hg(g)0 in the light isotopes relative to the total condensed fumarolic Hg(fum)T gas complements the speciation data and demonstrates a gas-particle fractionation occurring after the gas expulsion in ambient T° atmosphere. A first order Rayleigh equilibrium condensation isotope fractionation model yields a fractionation factor αcond-gas of 1.00135 ± 0.00058.  相似文献   

12.
A double-spike method was used to obtain Mo isotope data for sediments and waters of the seasonally anoxic Chesapeake Bay, and its primary tributary, the Susquehanna River. The dissolved Mo distribution in the estuary is non-conservative, reflecting minor Mo loss to the sediments, although removal of Mo to the sediments does not have a large influence on the isotopic composition of the water column. The δ98Mo of dissolved Mo in most of the estuary is dominated by seawater. Six samples with salinity > 15 have an average δ98Mo = + 2.17‰ (± 0.12), which agrees well with a δ98Mo value for the CASS-4 seawater standard of + 2.23‰. A single sample of Susquehanna River water has a δ98Mo of + 1.02‰, consistent with recent findings of positive δ98Mo in rivers worldwide. Susquehanna river sediments, in contrast, have δ98Mo ～ ? 0.1‰. The difference between the river water and sediment values implies that isotopic fractionation occurs within the river basin. The δ98Mo values for estuarine sediments are offset from values in the overlying water. Most samples deposited before 1925 have δ98Mo less than 0‰, similar to the Susquehanna sediments. Subsequently, there is an increase in the variability of δ98Mo, with values ranging up to + 0.8‰. The transition to increased variability coincides with the onset of authigenic Mo deposition, which was previously attributed to escalating summertime anoxia. Authigenic Mo concentrations correlate poorly with δ98Mo in core samples, suggesting that independent mechanisms influence the two parameters. Authigenic Mo concentrations may be controlled by shifting pore water H2S levels, while δ98Mo may be primarily affected by annual variations in Mn refluxing.  相似文献   

13.
We have investigated the solar activity signal in tree ring data from two locations in Chile. The tree ring time series extended over a period of ∼400 yr. Spectral and wavelet analysis techniques were employed. We have found evidence for the presence of the solar activity Schwabe (∼11 yr), Hale (∼22 yr), fourth-harmonic of the 208-yr Suess cycle (∼52 yr) and Gleissberg (∼80 yr) cycles. The Gleissberg cycle of tree ring data is in anti-phase with solar activity. Wavelet and cross-wavelet techniques revealed that the periods found are intermittent, possibly because solar activity signals observed in tree rings are mostly due to solar influence on local climate (rainfall, temperature, and cloud cover) where trees grow up. Further, cross-wavelet analysis between sunspot and tree ring time series showed that the cross power around the 11 yr solar cycle is more significant during periods of high solar activity (grand maximum) than during periods of low solar activity (grand minimum). As Glaciar Pio XI is practically at the Pacific Ocean level, the tree-ring response may be stronger due to the heating of the Pacific Ocean water following an increase of the solar radiation incidence rather than at the higher altitudes of Osorno region.  相似文献   

14.
Estimating past elevation not only provides evidence for vertical movements of the Earth's lithosphere, but also increases our understanding of interactions between tectonics, relief and climate in geological history. Development of biomarker hydrogen isotope-based paleoaltimetry techniques that can be applied to a wide range of sample types is therefore of continuing importance. Here we present leaf wax-derived n-alkane δD (δDwax) values along three soil altitudinal transects, at different latitudes, in the Wuyi, Shennongjia and Tianshan Mountains in China, to investigate δDwax gradients and the apparent fractionation between leaf wax and precipitation (εwax-p).We find that soil δDwax track altitudinal variations of precipitation δD along the three transects that span variable environment conditions and vertical vegetation spectra. An empirical δDwax-altitude relation is therefore established in which the average δDwax lapse rate of ? 2.27 ± 0.38‰/100 m is suitable for predicting relative paleoelevation change (relative uplift). The application of this empirical gradient is restricted to phases in the mountain uplift stage when the atmospheric circulation had not distinctly changed and to when the climate was not arid. An empirical δDwax–latitude–altitude formula is also calculated: δDwax = 3.483LAT ? 0.0227ALT ? 261.5, which gives the preliminary spatial distribution pattern of δDwax in modern China.Mean value of εwax-p in the extreme humid Wuyi Mountains is quite negative (? 154‰), compared to the humid Shennongjia (? 129‰) and the arid (but with abundant summer precipitation) Tianshan Mountains (? 130‰), which suggests aridity or water availability in the growing season is the primary factor controlling soil/sediment εwax-p. Along the Tianshan transects, values of εwax-p are speculated to be constant with altitude; while along the Wuyi and Shennongjia transects, εwax-p are also constant at the low-mid altitudes, but become slightly more negative at high altitudes which could be attributed to overestimates of precipitation δD or the vegetation shift to grass/conifer.Additionally, a reversal of altitude effect in the vertical variation of δDwax was found in the alpine zone of the Tianshan Mountains, which might be caused by atmospheric circulation change with altitude. This implies that the paleo-circulation pattern and its changes should also be evaluated when stable isotope-based paleoaltimetry is applied.  相似文献   

15.
High resolution OSL dating back to MIS 5e in the central Sea of Okhotsk   总被引：1，自引：0，他引：1  
Marine sediments contain important archives of past ocean and climate changes, but at high latitudes the absence of carbonate has prevented the construction of accurate chronological models. We have begun a study to (1) determine the accuracy of luminescence ages in deep-sea marine sediments, e.g. by comparison with marine oxygen isotope stratigraphy where possible, (2) describe changes in sedimentation rate through time, and (3) test whether it is possible to date back to marine isotope stage 5e (MIS 5e). We show here that optical dating of fine grains of quartz from the central Sea of Okhotsk is able to provide an accurate and precise chronology for the reconstruction of the palaeoceanic and palaeoclimatic environment at our site. The upper 6.5 m of the 18.42 m long core MR0604-PC07A is believed, based on its magnetic susceptibility and the oxygen isotope (δ18O) records to contain the last ～150 ka. Forty OSL samples were taken from this upper part of the core. The single-aliquot regenerative-dose (SAR) procedure is used for equivalent dose (De) determination. The luminescence characteristics of fine-grained quartz (4–11 μm) extracted from the core are described. The OSL signal is dominated by the fast component and a dose recovery test shows that we can accurately measure a known dose given in the laboratory prior to any heat treatment. Dose rates were determined using high-resolution gamma spectrometry, and vary between 0.4 and 1.6 Gy/ka. The OSL ages from this section lie between ～140 ka and ～15 ka and are in very good agreement with the δ18O stratigraphy up to MIS 5e. A clear change in sedimentation rate is identified: between ～139 and 110 ka, the sedimentation rate was ～0.09 m/ka, but then from ～110 to 15 ka, the sedimentation rate decreases to a constant value of ～0.04 m/ka. Our data confirm that OSL dating using widely distributed fine-grain quartz has great potential for dating deep-sea sediments. Because luminescence methods use clastic materials, they do not depend on the presence of biogenic carbonate. As a result it is now likely that we can establish a chronology in regions of the ocean that were previously undatable.  相似文献   

16.
High precision Mg isotope measurements by multi-collector ion microprobe show that refractory olivines from the Allende chondrite, either olivines isolated in the matrix (2 samples studied) or olivines in type I chondrules (6 samples studied), have variable δ26Mg* enrichments and deficits (calculated in permil as the 26Mg deviation from the instrumental mass fractionation line) relative to the Earth. Most average δ26Mg* (noted δ26Mg*av) values (between 10 and 20 analyses per chondrule) are negative but the total range is from ?0.029 (± 0.010) ‰ (2 sigma errors) to + 0.011 (± 0.011) ‰ with an exception of one olivine at + 0.043 (± 0.023) ‰. These variations in δ26Mg*av reflect the formation of the olivines from reservoirs enriched in various amounts of 26Mg by the decay of short-lived 26Al (T1/2 = 0.73 Ma). Similarly, 30 analyses of olivines from the Eagle Station pallasite show a δ26Mg*av value of ?0.033 ± 0.008‰, as negative as some olivines from Allende chondrules and the Solar system initial δ26Mg* value of ?0.038 ± 0.004‰ (defined at the time of formation of type B Ca–Al-rich inclusions – CAIs – when 26Al/27Al = 5.23 × 10?5, Jacobsen et al., 2008).Because olivines are Al-poor and because their Mg isotopic compositions are not reset during the chondrule forming events, their δ26Mg*av can be used to calculate model crystallization ages relative to various theoretical Mg isotope growth curves. The two end-member scenarios considered are (i) a “nebular” growth in which the Al/Mg ratio remains chondritic and (ii) a “planetary” growth in which a significant increase of the Al/Mg ratio can be due to, for instance, olivine magmatic fractionation. The low δ26Mg*av value of olivines from the Eagle Station pallasite demonstrate that metal-silicate differentiation occurred as early as ~ 0. 15- 0. 23+ 0. 29 Ma after CAIs in either of the growth scenarios. Similarly the variable δ26Mg*av values of refractory olivines can be understood if they were formed in planetesimals which started to differentiate as early as the Eagle Station parent body. Accretion of these planetesimals must have been coeval to the formation of CAIs and their disruption could explain why their fragments (Mg-rich olivines) were distributed in the chondrule forming regions of the disk.  相似文献   

17.
We present molybdenum isotope data for four sediment profiles from continental margin settings. Each profile has a distinctive average isotope composition ranging from δ98 / 95Mo − 0.5‰ to 1.3‰ (relative to J and M laboratory standard). This range lies between the modern ocean water value (2.3‰) and the values typical of Mo adsorbed onto Mn oxides (− 0.7‰ ± 0.1‰). An important finding of this study is the apparent co-variation between the Mo isotope composition and the accumulation rate of authigenic Mo under reducing conditions. This relationship suggests that the chemical processes responsible for Mo accumulation under reducing conditions produce an isotope signature in marine sediments. In addition to the relationship between Mo accumulation and the Mo isotope signature there is also a relationship between these parameters and the rate of organic carbon oxidation and burial. These relationships suggest that the Mo isotope signature of reducing sediments may serve as a tracer for the cycling of organic carbon in continental margin sediments; however, additional data will be required to refine any such relationships.  相似文献   

18.
To improve our knowledge about the geochemical and environmental aftermath of Neoproterozoic global glaciations, we analyzed stable isotopes (δ13C, δ18O, δ34S) and elemental concentrations (Ca, Mg, S, Sr, Fe, and Mn) of the ～ 10-m-thick Zhamoketi cap dolostone atop the Tereeken diamictite in the Quruqtagh area, eastern Chinese Tianshan. Available chemostratigraphic data suggest that the Tereeken diamictite is probably equivalent to the Marinoan glaciation. Our new data indicate that organic and carbonate carbon isotopes of the Zhamoketi cap dolostone show little stratigraphic variations, averaging ? 28.2‰ and ? 4.6‰, respectively. In contrast, sulfur isotopes show significant stratigraphic variations. Carbonate associated sulfate (CAS) abundance decreases rapidly in the basal cap dolostone and δ34SCAS composition varies between + 9‰ and + 15‰ in the lower 2.5 m. In the overlying interval, CAS abundance remains low while δ34SCAS rises ～ 5‰ and varies more widely between + 10‰ and + 21‰. The range of δ34Spy of the cap dolostone overlaps with that of δ34SCAS, but direct comparison shows that δ34Spy is typically greater than δ34SCAS measured from the same samples. Hypotheses to explain the observations must account for both the remarkable sulfur isotope enrichment of pyrites and the inverse fractionation. We propose that CAS and pyrite were derived from two isotopically distinct reservoirs in a chemically stratified basin or a basin with a sulfate minimum zone. In this model, CAS was derived from shallow, oxic surface waters with moderate sulfate concentration and depleted in 34S due to the post-glacial influx of sulfur from continental weathering. In contrast, pyrite was derived from anoxic bottom waters (or a sulfate minimum zone) with low sulfate concentration and 34S enrichment due to long-term syn-glacial sulfate reduction. The rapid shift in CAS abundance and sulfur isotope composition within the cap dolostone is interpreted to reflect the mixing of the two reservoirs after initial deglaciation. Comparison with other post-Marinoan cap carbonates shows significant spatial heterogeneity in δ34SCAS, which together with strong temporal variation in δ34SCAS, points to generally low sulfate concentrations in post-Marinoan oceans.  相似文献   

19.
High resolution records (ca. 100 kyr) of Os isotope composition (187Os / 188Os) in bulk sediments from two tropical Pacific sites (ODP Sites 1218 and 1219) capture the complete Late Eocene 187Os / 188Os excursion and confirm that the Late Eocene 187Os / 188Os minimum, earlier reported by Ravizza and Peucker-Ehrenbrink [Earth Planet. Sci. Lett. 210 (2003) 151–165], is a global feature. Using the astronomically tuned age models available for these sites, it is suggested that the Late Eocene 187Os / 188Os minimum can be placed at 34.5 ± 0.1 Ma in the marine records. In addition, two other distinct features of the 187Os / 188Os excursion that are correlatable among sections are proposed as chemostratigraphic markers which can serve as age control points with a precision of ca. ± 0.1 Myr. We propose a speculative hypothesis that higher cosmic dust flux in the Late Eocene may have contributed to global cooling and Early Oligocene glaciation (Oi-1) by supplying bio-essential trace elements to the oceans and thereby resulting in higher ocean productivity, enhanced burial of organic carbon and draw down of atmospheric CO2. To determine if the hypothesis that enhanced cosmic dust flux in the Late Eocene was a cause for the 187Os / 188Os excursion can be tested by using the paired bulk sediment and leachate Os isotope composition; 187Os / 188Os were also measured in sediment leachates. Results of analyses of leachates are inconsistent between the south Atlantic and the Pacific sites, and therefore do not yield a robust test of this hypothesis. Comparison of 187Os / 188Os records with high resolution benthic foraminiferal δ18O records across the Eocene–Oligocene transition suggests that 187Os flux to the oceans decreased during cooling and ice growth leading to the Oi-1 glaciation, whereas subsequent decay of ice-sheets and deglacial weathering drove seawater 187Os / 188Os to higher values. Although the precise timing and magnitude of these changes in weathering fluxes and their effects on the marine 187Os / 188Os records are obscured by recovery from the Late Eocene 187Os / 188Os excursion, evidence of the global influence of glaciation on supply of Os to the ocean is robust as it has now been documented in both Pacific and Atlantic records.  相似文献   

20.
The South Sandwich volcanic arc is sited on a young oceanic crust, erupts low-K tholeiitic rocks, is characterized by unexotic pelagic and volcanogenic sediments on the down-going slab, and simple tectonic setting, and is ideal for assessing element transport through subduction zones. As a means of quantifying processes attending transfer of subduction-related fluids from the slab to the mantle wedge, boron concentrations and isotopic compositions were determined for representative lavas from along the arc. The samples show variable fluid-mobile/fluid-immobile element ratios and high enrichments of B/Nb (2.7 to 55) and B/Zr (0.12 to 0.57), similar to those observed in western Pacific arcs. δ11B values are among the highest so far reported for mantle-derived lavas; these are highest in the central part of the arc (+ 15 to + 18‰) and decrease toward the southern and northern ends (+ 12 to + 14‰). δ11B is roughly positively correlated with B concentrations and with 87Sr/86Sr ratios, but poorly coupled with other fluid-mobile elements such as Rb, Ba, Sr and U. Peridotites dredged from the forearc trench also have high δ11B (ca. + 10‰) and elevated B contents (38–140 ppm). Incoming pelagic sediments sampled at ODP Site 701 display a wide range in δ11B (+ 5 to ? 13‰; average = ? 4.1‰), with negative values most common. The unusually high δ11B values inferred for the South Sandwich mantle wedge cannot easily be attributed to direct incorporation of subducting slab materials or fluids derived directly therefrom. Rather, the heavy B isotopic signature of the magma sources is more plausibly explained by ingress of fluids derived from subduction erosion of altered frontal arc mantle wedge materials similar to those in the Marianas forearc. We propose that multi-stage recycling of high-δ11B and high-B serpentinite (possibly embellished by arc crust and volcaniclastic sediments) can produce extremely 11B-rich fluids at slab depths beneath the volcanic arc. Infiltration of such fluids into the mantle wedge likely accounts for the unusual magma sources inferred for this arc.  相似文献   

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