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1.
Mid-Holocene stable isotope record of corals from the northern Red Sea   总被引：1，自引：0，他引：1  
We present a study based on X-ray chronologies and the stable isotopic composition of fossil Porites spp. corals from the northern Gulf of Aqaba (Red Sea) covering the mid-Holocene period from 5750 to 4450 14C years BP (before present). The stable oxygen and carbon isotopic compositions of five specimens reveal regular annual periodicities. Compared with modern Porites spp. from the same environment, the average seasonal δ 18O amplitude of the fossil corals is higher (by ca. 0.35–0.60‰), whereas annual growth rates are lower (by ca. 3.5 to 2 mm/year). This suggests stronger seasonality of sea surface temperatures and increased variability of the oxygen isotopic composition of the sea water due to changes in the precipitation and evaporation regime during the mid-Holocene. Most likely, summer monsoon rains reached the northern end of the Red Sea at that time. Average annual coral growth rates are diminished probably due to an increased input and resuspension of terrestrial debris to the shallow marine environment during more humid conditions. Our results corroborate published reports of paleodata and model simulations suggesting a northward migration of the African monsoon giving rise to increased seasonalities during the mid-Holocene over northeastern Africa and Arabia. Received: 4 January 1999 / Accepted: 13 September 1999  相似文献   

2.
A new geochemical record from the paaleolake Santiaguillo documents the hydrological variability of sub‐tropical northern Mexico over the last ～14 cal. ka. Summer‐season runoff, lake water salinity and deposition of sediments by aeolian activity were reconstructed from concentrations of K, Ca and Zr/K in bulk sediments. More‐than‐average runoff during c. 12.3–9.3 cal. ka BP represented an interval of enhanced summer precipitation. Arid intervals of c. 14–12.3 cal. ka BP and c. 6–4.3 cal. ka BP were characterized by average and more‐than‐average aeolian activity. Comparison with proxy records of summer as well as winter precipitation from tropical and sub‐tropical North America and sea surface temperatures from the Atlantic and Pacific provides insight into the source of moisture and possible forcing. The wet Pleistocene?Holocene transition and early Holocene was contemporary with warmer conditions in the Gulf of California. We suggest that the Atlantic had minimal influence on the summer precipitation of the western part of sub‐tropical northern Mexico and that the source of moisture was dominantly Pacific.  相似文献   

3.
Oxygen and hydrogen isotopic compositions of meteoric water are known to correlate with surface air temperature, except in tropical areas. This relationship has been described using a number of terms corresponding to specific observations, such as latitude, altitude and seasonal effects. However, these temperature effects do not seem to apply to precipitation in monsoonal areas of Asia. Questions have been raised as to whether the isotopic composition of meteoric water can be used to reconstruct paleomonsoon intensity. Tree rings of two modern spruce trees (Picea meyeri) and a 10,000-yr-old timber (Picea jezoensis) were analyzed for hydrogen isotopic composition. On average, the older tree is depleted in deuterium by 45‰ compared to the modern trees. We attribute this isotopic depletion to the strength of summer monsoons, which were more intense in the early Holocene than at present. Although this study is not definitive, it suggests that paleomonsoon intensity can be reconstructed by direct or proxy methods that yield the oxygen or hydrogen isotopic composition of meteoric water.  相似文献   

4.
A 4-year study in a central Texas cave quantifies multiple mechanisms that control dripwater composition and how these mechanisms vary at different drip sites. We monitored cave-air compositions, in situ calcite growth, dripwater composition and drip rate every 4-6 weeks. Three groups of drip sites are delineated (Groups 1-3) based on geochemical variations in dripwater composition. Quantitative modeling of mineral-solution reactions within the host carbonate rock and cave environments is used to identify mechanisms that can account for variations in dripwater compositions. The covariation of Mg/Ca (and Sr/Ca) and Sr isotopes is key in delineating whether Mg/Ca and Sr/Ca variations are dictated by water-rock interaction (i.e., calcite or dolomite recrystallization) or prior calcite precipitation (PCP). Group 1 dripwater compositions reflects a narrow range of the extent of water-rock interaction followed by varying amounts of prior calcite precipitation (PCP). Group 2 dripwater compositions are controlled by varying amounts of water-rock interaction with little to no PCP influence. Group 3 dripwater compositions are dictated by variable extents of both water-rock interaction and PCP. Group 1 drip sites show seasonal variations in dripwater Mg/Ca and Sr/Ca, whereas the other drip sites do not. In contrast to the findings of most previous dripwater Mg/Ca-Sr/Ca studies, these seasonal variations (at Group 1 drip sites) are independent of changes in water flux (i.e., rainfall and/or drip rate), and instead significantly correlate with changes in cave-air CO2 concentrations. These results are consistent with lower cave-air CO2, related to cool season ventilation of the cave atmosphere, enhancing calcite precipitation and leading to dripwater geochemical evolution via PCP. Group 1 dripwater Mg/Ca and Sr/Ca seasonality and evidence for PCP as a mechanism that can account for that seasonality, have two implications for many other regions where seasonal ventilation of caves is likely: (1) speleothem trace-element records may provide seasonal signals, and (2) such records may be biased toward recording climate conditions during the season when calcite is depositing. Additionally, we use our results to construct a forward model that illustrates the types of speleothem Mg/Ca and Sr/Ca variations that would result from varying controls on dripwater compositions. The model provides a basis for interpreting paleo-dripwater controls from high frequency Mg/Ca and Sr/Ca variations for speleothems from caves at which long term monitoring studies are not feasible.  相似文献   

5.
Waters from high‐altitude alpine lakes are mainly recharged by meteoric water. Because of seasonal variations in precipitation and temperature and relatively short hydraulic residence times, most high‐altitude lakes have lake water isotopic compositions (δ18Olake) that fluctuate due to seasonality in water balance processes. Input from snowmelt, in particular, has a significant role in determining lake water δ18O. Here we compare two high‐resolution δ18Odiatom records from lake sediments in the Swedish Scandes with instrumental data from the last century obtained from nearby meteorological stations. The time period AD 1900–1990 is characterised by an increase in winter precipitation and high winter/summer precipitation ratios and this is recorded in δ18Odiatom as decreasing trends. Lowest δ18Odiatom values and highest amount of winter precipitation are found around AD 1990 when the winter North Atlantic Oscillation index was above +2. We conclude that for the last 150 a the main factor affecting the δ18Odiatom signal in these sub‐Arctic high‐altitude lakes with short residence times has been changes in amount of winter precipitation and that δ18Odiatom derived from high‐altitude lakes in the Swedish Scandes can be used as a winter precipitation proxy. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

6.
贺兰山地区树轮碳氧同位素与夏季风降水的相关性讨论   总被引：1，自引：0，他引：1  
分析了贺兰山地区油松树轮的稳定碳氧同位素组成对环境因素的响应关系 , 发现树轮碳氧同位素组成均与当年 5～ 9月总降水量具有较好的响应关系 , 碳同位素组成与 5～ 9月总降水量呈负相关关系 ,而氧同位素组成与 5～ 9月总降水量呈正相关关系 ,二者都可较好地反映该地区夏季风降水量的变化.同时 ,碳氧同位素的相关性分析表明二者具有一定程度的负相关性.树轮碳氧同位素的分馏机理十分复杂,其同位素组成不仅与降水量有关,同时还受其他环境因素的影响,单纯利用一种同位素指标来提取相应的气候信息,存在很大的不确定性.在本研究中 ,同时采用两种同位素指标来研究其气候意义 ,使得出的结论更加可靠.因此 ,夏季风降水量是控制该地区树轮稳定碳氧同位素组成的主要因素.  相似文献   

7.
This paper describes an indirect method to calculate the isotopic composition of rainfall by using the isotopic composition of karst springs fed by waters circulating in the most important regional aquifer of central Italy, i.e. the Mesozoic limestone sequence that forms the backbone of the Apennines. By using δ18O and δD data and the δ18O (and/or δD) average gradient for elevation, evaluated through the use of literature rainfall data and new measurements from a typical Alpine valley in northern Italy, the altitude of precipitation of their parent water has been re-calculated. Vertical descents of more than 2000 m, from recharge to discharge, have been assessed in some high flow-rate cold springs in the morphologically steep Adriatic sector of central Italy. A clear correlation between the vertical descents and more negative isotopic compositions at their relative emergence elevations is highlighted. In contrast, in the Tyrrhenian sector lower karstic drops (generally lower than 500 m) correlate with less negative isotopic composition of recharge areas.The δ18O iso-contour map of the “recalculated” parent rainfall in central Italy is more detailed than any possible isotopic map of rainfall made using pluviometers, unless large number of rainfall collectors were deployed on mountaintops. The data also show that the isotopic composition of rainfall depends on the source of the storm water. In particular, precipitation is isotopically heavier when originating in the Mediterranean Sea, and lighter when formed in the Atlantic Ocean. Consequently, the collision between air masses with such a different isotopic signature results in a relatively small latitudinal fractionation effect. The peninsular part of central Italy is very narrow, with several mountains and massifs more that 2000 m high, and any latitudinal variation in the isotopic composition between rainfall sourced in the Atlantic Ocean and in the Mediterranean Sea is much lower than that due to the isotopic fractionation due to elevation.  相似文献   

8.
Numerous studies have shown that precipitation isocapes drive δD and δ18O patterns in surficial waters and in terrestrial food webs. While the GNIP (Global Network for Isotopes in Precipitation) dataset provided a key foundation for linking precipitation-terrestrial isoscapes globally, it has insufficient spatial coverage in many countries like Mexico. To overcome this limitation, we hypothesized that shallow phreatic groundwaters in Mexico could be used as an isotopic integrator of long-term seasonally weighted precipitation inputs to the landscape to aid in calibrating spatial H and O isotope datasets for terrestrial, biological and hydrological research. Groundwater was sampled from 234 sites in Mexico at ~ 50 km latitudinal spacing to obtain high spatial resolution and country-wide coverage for the construction of a groundwater isoscape. Our data revealed that shallow groundwater infiltration in Mexico appears largely unaffected by evaporation and reflects seasonally weighted precipitation inputs. These precipitation inputs are primarily biased to summertime when highest rainfall occurs, but a small degree of post-precipitation evaporation revealed a lower d-excess zone that corresponded to the interior semi-arid ecozone. We developed a predictive general linear model (GLM) for hydrogen and oxygen isotopic spatial patterns in Mexican groundwater and then compared the results to a validation subset of our field data, as well external data reported in the literature. The GLM used elevation, latitude, drainage basin (Atlantic vs. Pacific), and rainfall as the most relevant predictive variables. The GLM explained 81% of the overall isotopic variance observed in groundwater, 68% of the variance within our validation subset, and 77% of the variance in the external data set. Our predictive GLM is sufficiently accurate to allow for future ecological, hydrological and forensic isoscape applications in Mexico, and may be an approach that is applicable to other countries and regions where GNIP stations are lacking.  相似文献   

9.
An intensive investigation of the spatial and temporal variations of δD and δ 18O in precipitation was conducted during 2002–2004 in six sites in the Heihe River Basin, Northwestern China. The δD and δ 18O values for 301 precipitation samples ranged from +59 to −254 and +6.5 to −33.4‰, respectively. The relationship between δD and δ 18O defines a well-constrained line given by dD = 7.82d18\textO + 7.63 \delta D = 7.82\delta {}^{18}{\text{O}} + 7.63 , which is nearly identical to the meteoric water line in the Northern China. This wide range indicates that stable isotopes in precipitation were primarily controlled by different condensation mechanisms as a function of air temperature and varying sources of moisture. The results of backward trajectory of each precipitation day at Xishui show that the moisture of the precipitation in cold season (October–March) mainly originated from the west while the moisture source was more complicated in warm season (April–September). The simulation of seasonal δ 18O variation shows that the stable isotope composition of precipitation tended to a clear sine-wave seasonal variation. The spatial variation of δ 18O shows that the weighted average δ 18O values decreases with the increasing altitude of sampling sites. The great difference of air temperature which led to the differences of condensation mechanisms and local recycled continental moisture may have influence upon the isotopic composition of rain events in different sites.  相似文献   

10.
青藏高原水汽输送与冰芯中稳定同位素记录*   总被引：7，自引：7，他引：7       下载免费PDF全文
降水中稳定同位素作为水中的组成成分,与水汽来源的变化存在直接的关系。根据在青藏高原降水中稳定同位素的研究,青藏高原南北降水中δ18 O和过量氘(d)都存在着显著的空间变化,这种空间变化与西南季风夏季向北推进的位置有关。在时间变化上,青藏高原不同地区降水中δ18 O和d的季节变化特征也与水汽来源的季节变化有关,而且这种季节变化主要受控于西南季风水汽与西风带输送水汽之间的相互作用,在中国最北端的阿尔泰山区还受到极地气团的影响。由于不同的大气环流造成的水汽来源的差异,青藏高原冰芯中稳定同位素变化也存在空间差异。北部地区冰芯中稳定同位素的年际变化与当地气象站记录显示良好的对应关系,而南部冰芯中稳定同位素的变化与当地气象站降水量在年际变化上显示反相关关系。  相似文献   

11.
The neodymium concentration, CNd, and isotopic composition, εNd, in seawater have been determined in the water column at five sites in the Barents Sea-Fram Strait area where most of the water exchange between the Arctic Ocean and the North Atlantic takes place. In the main Arctic Ocean inflow branch across the Barents Sea the concentration and isotopic composition (CNd = 15.5 pmol/kg and εNd = −10.8) are similar to those reported for the northeastern Nordic Seas, which is consistent with this region being a source area for the Arctic inflow. Due to the addition of Nd from Svalbard shelf sediments, the CNd in the surface waters above 150 m, in the Fram Strait inflow branch is higher by a factor of 2 and the εNd is shifted to lower values (−11.8).In the stratified Nansen Basin, where cold low salinity water overlies warmer Atlantic water the CNd and εNd do not vary with the vertical temperature-salinity structure but are essentially constant and similar to those of the Atlantic inflow throughout the entire water column, down to 3700 m depth, which indicates that the Nd is to a large extent of Atlantic origin.Compared to the Atlantic inflow water, the Nd in the major Arctic Ocean outflow, the Fram Strait, show higher CNd in the surface waters above 150 m, and a higher εNd (−9.8) throughout the entire water column down to 1300 m depth. Sources for the more radiogenic Nd isotopic composition in deep water of the Fram Strait outflow most likely involve boundary exchange with sediments on the shelf and slope as the water passes along the Canadian archipelago. River water is a possible source in the surface water but it also seems likely that Pacific water Nd, modified by interactions on the shelf, is an important component in the Fram Strait surface outflow. Changes in the relative proportions of inflow of river water and flow of Pacific water through the Arctic Ocean could thus influence the isotopic composition of Nd in the North Atlantic.  相似文献   

12.
The DUPAL anomaly, a radiogenic isotope anomaly discovered in the Indian Ocean mantle, has been interpreted as due to a large-scale mantle heterogeneity. To provide new constraints on the DUPAL origin, we analyzed isotope ratios of Li, Sr, and Nd in fresh N-MORB glasses recovered from the Rodrigues Triple Junction in the Indian Ocean, and from the North Atlantic. The Li isotopic compositions of the Indian Ocean DUPAL N-MORBs were comparable to those of the North Atlantic non-DUPAL N-MORBs. The source of the DUPAL signature in Indian Ocean MORBs and the E-MORB-type enriched mantle source have quite different Li isotopic compositions. The 143Nd/144Nd values of both sources are significantly lower than those of the North Atlantic N-MORBs. The δ7Li values of most oceanic island basalts with similar low 143Nd/144Nd signatures are also higher than those of the North Atlantic N-MORBs, except for several Koolau lavas. The Li isotope results support the recent proposal that significant amounts of recycled lower continental crust might produce the radiogenic isotope signatures of the Indian Ocean DUPAL source.  相似文献   

13.
洞庭湖湖区降水-地表水-地下水同位素特征   总被引：8，自引：0，他引：8  
为探明洞庭湖湖区水体稳定同位素时间和空间上的变化规律,弄清各水体间的相互关系,分别在2012年4月和8月对区域内具有代表性的采样点进行了地表水和地下水的采样。通过对样品进行D、18O同位素分析,结合全球大气降水同位素监测网（GNIP）公布的1988—1992年间长沙降水同位素数据,发现湖区年内受不同盛行风影响,降水及地表水的同位素存在较大的季节性差异,4月份同位素富集,8月份贫化。此外,河水、湖水同位素也呈现明显的空间差异。两个时期地表水的水线斜率均小于当地降水线,地表水在两个时期均存在蒸发作用。虽然地表水和地下水的来源均为大气降水,但与地表水相比,地下水同位素季节变化较小,地下水接受地表水补给是一个较为长期的过程。  相似文献   

14.
Authigenic carbonates were sampled in piston cores collected from both the Tunica Mound and the Mississippi Canyon area on the continental slope of the northern Gulf of Mexico during a Marion Dufresne cruise in July 2002. The carbonates are present as hardgrounds, porous crusts, concretions or nodules and shell fragments with or without carbonate cements. Carbonates occurred at gas venting sites which are likely to overlie gas hydrates bearing sediments. Electron microprobe, X-ray diffraction (XRD) and thinsection investigations show that these carbonates are high-Mg calcite (6–21 mol% MgCO3), with significant presence of framboidal pyrite. All carbonates are depleted in 13C (δ13C = − 61.9 to − 31.5‰ PDB) indicating that the carbon is derived mainly from anaerobic methane oxidation (AMO). Age estimates based on 14C dating of shell fragments and on regional sedimentation rates indicate that these authigenic carbonates formed within the last 1000 yr in the Mississippi Canyon and within 5500 yr at the Tunica Mound. The oxygen isotopic composition of carbonates ranges from + 3.4 to + 5.9‰ PDB. Oxygen isotopic compositions and Mg2+ contents of carbonates, and present in-situ temperatures of bottom seawater/sediments, show that some of these carbonates, especially from a core associated with underlying massive gas hydrates precipitated in or near equilibrium with bottom-water. On the other hand, those carbonates more enriched in 18O are interpreted to have precipitated from 18O-rich fluids which are thought to have been derived from the dissociation of gas hydrates. The dissociation of gas hydrates in the northern Gulf of Mexico within the last 5500 yr may be caused by nearby salt movement and related brines.  相似文献   

15.
Oil seeps from the southern Gulf of Mexico can be regarded as natural laboratories where the effect of crude oil seepage on chemosynthesis‐based communities and carbonate precipitation can be studied. During R/V Meteor cruise 114 the seep sites UNAM (Universidad Nacional Autónoma de México) Ridge, Mictlan Knoll and Tsanyao Yang Knoll (Bay of Campeche, southern Gulf of Mexico) were investigated and sampled for authigenic carbonate deposits containing large amounts of liquid oil and solid asphalt. The δ13C values of individual carbonate phases including: (i) microcrystalline matrix aragonite and calcite; (ii) grey, cryptocrystalline to microcrystalline aragonite; and (iii) clear, fibrous aragonite cement, are between ?30‰ and ?20‰, agreeing with oil as the primary carbon source. Raman spectra reveal that residual heavy oils from all sites are immature and most likely originate from the same reservoir. Geochemical batch modelling using the software code PHREEQC demonstrates how sulphate‐driven oxidation of oil‐derived low‐molecular to high‐molecular weight hydrocarbons affects carbonate saturation state, and shows that the oxidation state of carbon in hydrocarbon compounds and oxidation rates of hydrocarbons control carbonate saturation and precipitation at oil seeps. Phase‐specific trace and rare earth element contents of microcrystalline aragonite and calcite, grey cryptocrystalline aragonite and clear aragonite were determined, revealing enrichment in light rare earth elements for grey aragonite. By comparing trace element patterns of carbonates with those of associated oils, it becomes apparent that liquid hydrocarbons constitute an additional source of trace metals to sedimentary pore waters. This work not only demonstrates that the microbial degradation of oil at seeps may result in the precipitation of carbonate minerals, it also elucidates that trace metal inventories of seep carbonates archive diagnostic elemental patterns, which can be assigned to the presence of heavy hydrocarbons in interstitial pore waters.  相似文献   

16.
Hundreds of precipitation samples collected from meteorological stations in the Ordos Basin from January 1988 to December 2005 were used to set up a local meteoric water line and to calculate weighted average isotopic compositions of modern precipitation. Oxygen and hydrogen isotopes, with averages of ?7.8‰ and ?53.0‰ for δ18O and δD, respectively, are depleted in winter and rich in spring, and gradually decrease in summer and fall, illustrating that the seasonal effect is considerable. They also show that the isotopic difference between south portion and north portion of the Ordos Basin are not obvious, and the isotope in the middle portion is normally depleted. The isotope compositions of 32 samples collected from shallow groundwater (less than a depth of 150 m) in desert plateau range from ?10.6‰ to ?6.0‰ with an average of ?8.4‰ for δ18O and from ?85‰ to ?46‰ with an average of ?63‰ for δD. Most of them are identical with modern precipitation. The isotope compositions of 22 middle and deep groundwaters (greater than a depth of 275 m) fall in ranges from ?11.6‰ to ?8.8‰ with an average of ?10.2‰ for δ18O and from ?89‰ to ?63‰ with an average of ?76‰ for δD. The average values are significantly less than those of modern precipitation, illustrating that the middle and deep groundwaters were recharged at comparatively lower air temperatures. Primary analysis of 14C shows that the recharge of the middle and deep groundwaters started at late Pleistocene. The isotopes of 13 lake water samples collected from eight lakes define a local evaporation trend, with a relatively flat slope of 3.77, and show that the lake waters were mainly fed by modern precipitation and shallow groundwater.  相似文献   

17.
We present hafnium (Hf) and neodymium (Nd) isotopic compositions and concentrations in surface waters of the eastern Atlantic Ocean between the coast of Spain and South-Africa. These data are complemented by Hf and Nd isotopic and concentration data, as well as rare earth element (REE) concentrations, in Saharan dust.Hafnium concentrations range between a maximum of 0.52 pmol/kg in the area of the Canary Islands and a minimum value of 0.08 pmol/kg in the southern Angola Basin. Neodymium concentrations also show a local maximum in the area of the Canary Islands (26 pmol/kg) but are even higher between ∼20°N and ∼4°N reaching maximum concentrations of 35 pmol/kg. These elevated concentrations provide evidence of inputs from weathering of the Canary Islands and from the partial dissolution of dust from the Sahara/Sahel region. The inputs from ocean island weathering are also reflected in radiogenic Hf and Nd isotopes.The Hf isotopic compositions of dust samples themselves are highly variable, ranging between εHf = −20 and −0.6. The combined Hf and Nd isotopic compositions of dust plot close to the “terrestrial array” during periods of appreciable dust load in the atmosphere. During low atmospheric dust loading combined Hf and Nd isotopic compositions similar to seawater are observed. Most of the variability can be explained in terms of variable degrees of zircon loss from the dust samples, which in turn is linked to sorting during atmospheric transport to the eastern Atlantic Ocean and possibly presorting by sedimentary redistribution on the continent. In addition, increasing relative proportions of radiogenic clay minerals with decreasing grain size may contribute to the radiogenic Hf isotopic compositions observed.While the Nd isotopic composition in the surface ocean reflects the Nd isotopic composition of the Saharan dust adjacent to the Sahara/Sahel region, the release of Hf from that dust appears to be incongruent and results in surface ocean Hf isotopic compositions which are ∼10 εHf more radiogenic than the bulk dust. Radiogenic Hf appears to be released from clays and possibly from trace apatite. Rare earth element patterns of dust samples indicate the presence of apatite but provide no evidence for ferromanganese grain coatings, suggesting that such coatings are insignificant in the release of Hf and Nd from Saharan dust to the surface ocean.The Nd isotopic composition of the surface waters becomes less radiogenic south of the equator, most likely reflecting the release of Nd from Congo river sediments. The release of Hf from Saharan dust and the Congo river sediments, however, does not produce distinct Hf isotopic signatures in the surface ocean, implying that the mobile fraction of Hf integrated over large continental areas is isotopically uniform. The Hf isotopic uniformity in the surface ocean means that the limited variability in deep water isotopic compositions is consistent with a short deep water residence time and reflects homogenous continental inputs rather than efficient deep water homogenization.  相似文献   

18.
Chromite separates within the Peridotite Zone of the 2,700 Ma-old Stillwater Complex are characterized by low 187Re/188Os (0.009 to 1.74) and relatively high Os concentrations (8.74 to 78.2 ppb). Their calculated initial Os isotopic compositions likely reflect the compositions of the magmas from which they crystallized. The chromites show variable initial Os isotopic compositions (%Os of +2.0 to +16.4) over the vertical extent of the Peridotite Zone, implicating at least two sources of Os. Both the range of %Os and values of %Os decrease upsection. These variations in %Os were caused by mixing of variable proportions of two magmas having different Os isotopic compositions. One of the magmatic components was a more primitive magma with a nearly chondritic Os isotopic composition. The other magma had a radiogenic Os isotopic composition as a result of assimilation of crust, perhaps of sedimentary rocks beneath the Stillwater Complex. The gradual decrease in the initial %Os values of the chromite layers with increasing stratigraphic height implies a decreasing relative contribution from the contaminated magma throughout the growth of the Peridotite Zone. Small variations in %Os between different chromite occurrences within the H multicyclic unit reflects the petrologic requirement that chromite layers crystallize from slightly different proportions of the magmas, compared to chromite from olivine- and orthopyroxene-rich layers.  相似文献   

19.
Oxygen isotopic compositions of quartz from silty sediments buried to 5400 m depth from two wells in the Gulf of Mexico each showed δ518O variations of less than 1.7%. Clay diagenesis has been reported within this depth. The observed variations in the quartz do not appear to be primarly diagenetic effects, but rather are mainly depositional features reflecting variations in the sources of the sediments. Sources may be influenced by the variation of distance from the shore at different depths in a given sampling location and by sediment production by continental glaciations. Stability of the oxygen isotopic composition of quartz in the 10–20 μm size range under long-time humid, temperate weathering conditions was studied by analysis of saprolites formed from Pennsylvanian to Precambrian crystalline rocks. In four of the five cases, the 10–20 μm fraction was found to have only 0.1–0.5%. greater δ18O than the corresponding 20–50 μm fraction. This increase may be attributable either to a slight oxygen isotopic exchange with ambient ground waters or original differences within the rock since the saprolites were sufficiently coherent to make an influx of extraneous detrital silt unlikely. The amount of oxygen isotopic exchange in silt size quartz over periods of many million years of shallow burial or weathering appears to be small enough to permit the use of the oxygen isotopic ratio of quartz in tracing the origin of eolian and fluvial additions of minerals to continental soils and pelagic sediments.  相似文献   

20.
Three estuaries near Naples, Florida with variably modified watersheds have been investigated to understand the chemical consequences of altering drainage patterns. Blackwater River (near natural drainage, control site), Henderson Creek (moderately modified watershed), and Faka-Union Canal (severe channelization) were sampled for temperature, salinity, δ18O, δ13C of dissolved inorganic carbon (DIC), molality of CO2 (ΣCO2), and Mg:Ca and Sr:Ca ratios between freshwater and marine water end members over a 17-mo period. Carbon isotope composition followed similar seasonal patterns as salinity. Freshwater and seawater end members are more negative than the global average, likely reflecting equilibration with local carbon sources derived from mangrove leaf litter and groundwater. δ13C responds to differences in primary productivity between estuaries. Henderson Creek has higher primary productivity than Blackwater River (probable due to higher sewage input and agricultural runoff) and has more positive δ13C and lower ΣCO2. δ18O is affected by seasonal input of freshwater from atmospheric precipitation, evaporation, and groundwater. Late summer and fall rains lower the δ18O of estuarine water, whereas evaporative conditions in the dry season elevate δ18O to values that can be more positive upstream than those from the Gulf of Mexico (estuarine inversion). Evaporation produces water in the Gulf of Mexico that is >1‰ more positive than the global sea surface average most of the year. The very negative δ18O values in Blackwater River and Henderson Creek likely reflect atmospheric and groundwater contribution. Mg:Ca and Sr:Ca ratios of Gulf water from all three estuaries are similar to global averages at low latitudes. Freshwater end members among estuaries are different in that Blackwater River has higher ratios, suggesting a groundwater contribution. Dolomitic rocks in the subsurface likely provide a source of Mg ions.  相似文献   

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