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1.
A systematic investigation on silica contents and silicon isotope compositions of bamboos was undertaken. Seven bamboo plants and related soils were collected from seven locations in China. The roots, stem, branch and leaves for each plant were sampled and their silica contents and silicon isotope compositions were determined. The silica contents and silicon isotope compositions of bulk and water-soluble fraction of soils were also measured. The silica contents of studied bamboo organs vary from 0.30% to 9.95%. Within bamboo plant the silica contents show an increasing trend from stem, through branch, to leaves. In bamboo roots the silica is exclusively in the endodermis cells, but in stem, branch and leaves, the silica is accumulated mainly in epidermal cells. The silicon isotope compositions of bamboos exhibit significant variation, from −2.3‰ to 1.8‰, and large and systematic silicon isotope fractionation was observed within each bamboo. The δ30Si values decrease from roots to stem, but then increase from stem, through branch, to leaves. The ranges of δ30Si values within each bamboo vary from 1.0‰ to 3.3‰. Considering the total range of silicon isotope composition in terrestrial samples is only 7‰, the observed silicon isotope variation in single bamboo is significant and remarkable. This kind of silicon isotope variation might be caused by isotope fractionation in a Rayleigh process when SiO2 precipitated in stem, branches and leaves gradually from plant fluid. In this process the Si isotope fractionation factor between dissolved Si and precipitated Si in bamboo (αpre-sol) is estimated to be 0.9981. However, other factors should be considered to explain the decrease of δ30Si value from roots to stem, including larger ratio of dissolved H4SiO4 to precipitated SiO2 in roots than in stem. There is a positive correlation between the δ30Si values of water-soluble fractions in soils and those of bulk bamboos, indicating that the dissolved silicon in pore water and phytoliths in soil is the direct sources of silicon taken up by bamboo roots. A biochemical silicon isotope fractionation exists in process of silicon uptake by bamboo roots. Its silicon isotope fractionation factor (αbam-wa) is estimated to be 0.9988. Considering the distribution patterns of SiO2 contents and δ30Si values among different bamboo organs, evapotranspiration may be the driving force for an upward flow of a silicon-bearing fluid and silica precipitation. Passive silicon uptake and transportation may be important for bamboo, although the role of active uptake of silicic acid by roots may not be neglected. The samples with relatively high δ30Si values all grew in soils showing high content of organic materials. In contrast, the samples with relatively low δ30Si values all grew in soil showing low content of organic materials. The silicon isotope composition of bamboo may reflect the local soil type and growth conditions. Our study suggests that bamboos may play an important role in global silicon cycle.  相似文献   

2.
Several important equilibrium Si isotope fractionation factors among minerals, organic molecules and the H4SiO4 solution are complemented to facilitate the explanation of the distributions of Si isotopes in Earth’s surface environments. The results reveal that, in comparison to aqueous H4SiO4, heavy Si isotopes will be significantly enriched in secondary silicate minerals. On the contrary, quadra-coordinated organosilicon complexes are enriched in light silicon isotope relative to the solution. The extent of 28Si-enrichment in hyper-coordinated organosilicon complexes was found to be the largest. In addition, the large kinetic isotope effect associated with the polymerization of monosilicic acid and dimer was calculated, and the results support the previous statement that highly 28Si-enrichment in the formation of amorphous quartz precursor contributes to the discrepancy between theoretical calculations and field observations. With the equilibrium Si isotope fractionation factors provided here, Si isotope distributions in many of Earth’s surface systems can be explained. For example, the change of bulk soil δ30Si can be predicted as a concave pattern with respect to the weathering degree, with the minimum value where allophane completely dissolves and the total amount of sesqui-oxides and poorly crystalline minerals reaches their maximum. When, under equilibrium conditions, the well-crystallized clays start to precipitate from the pore solutions, the bulk soil δ30Si will increase again and reach a constant value. Similarly, the precipitation of crystalline smectite and the dissolution of poorly crystalline kaolinite may explain the δ30Si variations in the ground water profile. The equilibrium Si isotope fractionations among the quadra-coordinated organosilicon complexes and the H4SiO4 solution may also shed light on the Si isotope distributions in the Si-accumulating plants.  相似文献   

3.
Fractionation of silicon isotopes during biogenic silica dissolution   总被引：2，自引：0，他引：2  
Silicon isotopes have been investigated for their potential to reveal both past and present patterns of silicic acid utilization, primarily by diatoms, in surface waters of the ocean. Interpretation of this proxy has thus far relied on characteristic trends in the isotope composition of the dissolved and particulate silicon pools in the upper ocean, as driven by biological fractionation during the production of biogenic silica (bSiO2, or opal) by diatoms. However, other factors which may influence the silicon isotope composition of diatom opal, particularly post-formational aging and maturation processes, remain largely uninvestigated. Here, we report a consistent fractionation of silicon isotopes during the physicochemical dissolution of diatom bSiO2 suspended in seawater under closed conditions. This fractionation acts counter to that occurring during bSiO2 production and at about half its absolute magnitude, with dissolution discriminating against the release of the heavier isotopes of silicon at an enrichment factor εDSi–BSi of −0.55‰, corresponding to a fractionation factor α30/28 of 0.99945. The enrichment factor did not vary with source material, indicating the lack of a significant species effect, or with temperature from 3 to 20 °C. Thus, the dissolution of bSiO2 produces dissolved silicon with a δ30Si value that is 0.55‰ more negative than its parent bSiO2, an effect that must be accounted for when interpreting oceanic δ30Si distributions. The δ30Si values of both the dissolved and particulate silicon pools increased linearly as dissolution progressed, implying a measurable (±0.1‰) change in the relative δ30Si of opal samples whenever the difference in preservation efficiency between them is >20%. This effect could account for 10–30% of the difference in diatom δ30Si values observed between glacial and interglacial conditions. It is unlikely, however, that the inferred maximum possible change in δb30SiO2 of +0.55‰ would be manifested in situ, as a high mean percentage of dissolution would include complete loss of the more soluble members of the diatom assemblage.  相似文献   

4.
The silicon isotope fractionation between rice plant and nutrient solution was studied experimentally. Rice plants were grown to maturity with the hydroponic culture in a naturally lit glasshouse. The nutrient solution was sampled for 14 times during the whole rice growth period. The rice plants were collected at various growth stages and different parts of the plants were sampled separately. The silica contents of the samples were determined by the gravimetric method and the silicon isotope compositions were measured using the SiF4 method.In the growth process, the silicon content in the nutrient solution decreased gradually from 16 mM at starting stage to 0.1-0.2 mM at harvest and the amount of silica in single rice plant increased gradually from 0.00013 g at start to 4.329 g at harvest. Within rice plant the SiO2 fraction in roots reduced continuously from 0.23 at the seedling stage, through 0.12 at the tiller stage, 0.05 at the jointing stage, 0.023 at the heading stage, to 0.009 at the maturity stage. Accordingly, the fraction of SiO2 in aerial parts increased from 0.77, through 0.88, 0.95, 0.977, to 0.991 for the same stages. The silicon content in roots decreased from the jointing stage, through the heading stage, to the maturity stage, parallel to the decrease of silicon content in the nutrient solution. At the maturity stage, the silicon content increased from roots, through stem and leaves, to husks, but decreased drastically from husks to grains. These observations show that transpiration and evaporation may play an important role in silica transportation and precipitation within rice plants.It was observed that the δ30Si of the nutrient solution increased gradually from −0.1‰ at start to 1.5‰ at harvest, and the δ30Si of silicon absorbed by bulk rice plant increased gradually from −1.72‰ at start to −0.08‰ at harvest, reflecting the effect of the kinetic silicon isotope fractionation during silicon absorption by rice plants from nutrient solutions. The calculated silicon isotope fractionation factor between the silicon instantaneously absorbed by rice roots and the silicon in nutrient solution vary from 0.9983 at start to 0.9995 at harvest, similar to those reported for bamboo, banana and diatoms in direction and extent. In the maturity stage, the δ30Si value of rice organs decreased from −1.33‰ in roots to −1.98‰ in stem, and then increased through −0.16‰ in leaves and 1.24‰ in husks, to 2.21‰ in grains. This trend is similar to those observed in the field grown rice and bamboo.These quantitative data provide us a solid base for understanding the mechanisms of silicon absorption, transportation and precipitation in rice plants and the role of rice growth in the continental Si cycle.  相似文献   

5.
In this study, we used first-principles calculations based on density functional theory to investigate silicon and oxygen isotope fractionation factors among the most abundant major silicate minerals in granites, i.e., quartz and plagioclase (including albite and anorthite), and an important accessory mineral zircon. Combined with previous results of minerals commonly occurring in the crust and upper mantle (orthoenstatite, clinoenstatite, garnet, and olivine), our study reveals that the Si isotope fractionations in minerals are strongly correlated with SiO4 tetrahedron volume (or average Si–O bond length). The 30Si enrichment order follows the sequence of quartz > albite > anorthite > olivine ≈ zircon > enstatite > diopside, and the 18O enrichment follows the order of quartz > albite > anorthite > enstatite > zircon > olivine. Our calculation predicts that measurable fractionation of Si isotopes can occur among crustal silicate minerals during high-temperature geochemical processes. This work also allows us to evaluate Si isotope fractionation between minerals and silicate melts with variable compositions. Trajectory for δ30Si variation during fractional crystallization of silicate minerals was simulated with our calculated Si isotope fractionation factors between minerals and melts, suggesting the important roles of fractional crystallization to cause Si isotopic variations during magmatic differentiation. Our study also predicts that δ30Si data of ferroan anorthosites of the Moon can be explained by crystallization and aggregation of anorthite during lunar magma ocean processes. Finally, O and Si isotope fractionation factors between zircon and melts were estimated based on our calculation, which can be used to quantitatively account for O and Si isotope composition of zircons crystallized during magma differentiation.  相似文献   

6.
The sequestration of silicon in soil clay-sized iron oxides may affect the terrestrial cycle of Si. Iron oxides indeed specifically adsorb aqueous monosilicic acid (H4SiO40), thereby influencing Si concentration in soil solution. Here we study the impact of H4SiO40 adsorption on the fractionation of Si isotopes in basaltic ash soils differing in weathering degree (from two weathering sequences, Cameroon), hence in clay and Fe-oxide contents, and evaluate the potential isotopic impact on dissolved Si in surrounding Cameroon rivers. Adsorption was measured in batch experiment series designed as function of time (0-72 h) and initial concentration (ic) of Si in solution (0.61-1.18 mM) at 20 °C, constant pH (5.5) and ionic strength (1 mM). After various soil-solution contact times, the δ30Si vs. NBS28 compositions were determined in selected solutions by MC-ICP-MS (Nu Plasma) in medium resolution, operating in dry plasma with Mg doping with an average precision of ±0.15‰ (±2σSEM). The quantitative adsorption of H4SiO40 by soil Fe-oxides left a solution depleted in light Si isotopes, which confirms previous study on synthetic Fe-oxides. Measured against its initial composition (δ30Si = +0.02 ± 0.07‰ (±2σSD)), the solutions were systematically enriched in 30Si reaching maximum δ30Si values ranging between +0.16‰ and +0.95‰ after 72 h contact time. The enrichment of the solution in heavy isotopes increased with increasing values of three parameters: soil weathering degree, iron oxide content, and proportion of short-range ordered Fe-oxide. The Si-isotopic signature of the solution was partly influenced by Si release, possibly through mineral dissolution and Si desorption from oxide surfaces, depending on soil type, highlighting the complex pattern of natural soils. Surrounding Cameroon rivers displayed a mean Si-isotopic signature of +1.19‰. Our data imply that in natural environments, H4SiO40 adsorption by soil clay-sized Fe-oxides at least partly impacts the Si-isotopic signature of the soil solution exported to water streams.  相似文献   

7.
Silicon isotope ratios (δ30Si) of bulk mineral materials in soil integrate effects from both silicon sources and processing. Here we report δ30Si values from a climate gradient of Hawaiian soils developed on 170 ka basalt and relate them to patterns of soil chemistry and mineralogy. The results demonstrate informative relationships between the mass fraction of soil Si depletion and δ30Si. In upper (<1 m deep) soil horizons along the climate gradient, Si depletion correlates with decreases of residual δ30Si values in low rainfall soils and increases in high rainfall soils. Strong positive correlation between soil δ30Si and dust-derived quartz and mica content show that both trends are largely controlled by the abundance of these weathering-resistant minerals. The data also lend support to the idea that fractionation of Si isotopes in secondary phases is controlled by partitioning of silicon between dissolved and precipitated products during the initial weathering of primary basalt. Secondary mineral δ30Si values from lower (>1 m deep) soil horizons generally correlate with the isotope fractionation predicted by a study of dissolved Si in basalt-watershed rivers and driven by preferential 28Si removal from the dissolved phase during precipitation. In contrast, after correcting for the influence of dust, secondary mineral Si depletion and δ30Si values in shallow (<1 m deep) soil horizons showed evidence of biocycling induced Si redistribution and substantially lower δ30Si values than predicted. Low δ30Si values in shallow soil horizons compared to predictions can be attributed to repeated fractionation as secondary minerals undergo additional cycles of dissolution and precipitation. Primary mineral weathering, secondary mineral weathering, dust accumulation, and biocycling are major processes in terrestrial Si cycling and these results demonstrate that each can be traced by δ30Si values interpreted in conjunction with mineralogy and measures of Si depletion.  相似文献   

8.
Differences between the δ18O values of Si- and Fe-rich immiscible liquids in the system Fe2SiO4-KAlSi2O6-SiO2 (Fa-Lc-Q) in isothermal experiments at 0.1 MPa have been determined experimentally to be 0.6 permil. The observed partition of 18O into the Si-rich liquid is consistent with previous experience with the preferential partition of 18O into Si-rich minerals in isothermal equilibrium with minerals of less polymerized structure. Crystallochemical principles affect the distribution of oxygen isotopes in coexisting isothermal liquids in the same way as they apply to isothermally coexisting crystals. The effects of Soret (thermal) diffusion on the distribution of oxygen isotopes in silicate liquids above the solvus in the system Fa-Lc-Q under conditions of an imposed temperature gradient of ca. 250 °C over 4 mm and at 2 GPa have also been investigated experimentally. Both the magnitude and the direction of separation of oxygen isotopes as a result of Soret diffusion are unexpected. For each of the silicate liquids, the cold end of the charge is enriched in 18O by up to 4.7 permil, and the highest δ18O values are associated with the most silica-poor compositions. The distribution of oxygen isotopes appears to be similar in each liquid, regardless of their chemical compositions, which is in contrast to the behaviour of cations whose distributions are compositionally dependent and characterized by strong crystallochemical effects wherein network-forming species such as Si and Al separate to the hot end and Mg, Fe and Ca are segregated preferentially to the cold end. Structural units in the melts are evidently less selective between oxygen isotopes than between cations, because oxygen redistribution over all possible sites in these units proceeds according to mass. Self-diffusion coefficients of oxygen in basaltic liquids estimated from the Soret experiments are in accord with those from other isotope tracer experiments, and comparable to those of Si. The possible effects of Soret diffusion on the oxygen isotopic composition of metasomatic veins in the mantle are examined in light of these data, and indicate that decay of the thermal gradients in the veins exceeds that of the diffusion of oxygen needed to produce variations in the δ18O values of mantle minerals. Variations in oxygen isotope ratios in most natural systems as a result of Soret effects are unlikely. Received: 6 January 1997 /  Accepted: 28 June 1998  相似文献   

9.
The distribution of silicon isotopes along a meridional transect at 140°W longitude in the Eastern Equatorial Pacific was used to test the hypothesis that δ30Si of silicic acid in surface waters should correlate with net silica production rates (gross silica production minus silica dissolution) rather than rates of gross silica production due to the opposing Si isotope fractionations associated with silica production and silica dissolution. Variations in δ30Si appeared significantly correlated with net silica production rates in equatorial surface waters and not with gross production rates. Around the Equator, values of δ30Si as low as deep water values occurred in the upper mesopelagic in a zone of net silica dissolution and high detrital biogenic silica content, where the release of low δ30Si silicic acid from opal dissolution would be expected to decrease δ30Si. The δ30Si of the deep water at 140°W appears constant for depths >2000 m and is similar to the deep water at 110°W. This study brings to light the importance of considering Si fractionation during diatom silica dissolution, the biological fractionation during silica production and physical factors such as currents and mixing with adjacent water masses when interpreting silicon isotope distributions.  相似文献   

10.
This paper investigates kerogen carbon isotopes, the difference between carbonate and kerogen carbon isotopes (Δ13Ccarb-kero = δ 13Ccarb − δ 13Ckero) and the difference between carbonate and n-C19 alkane compound-specific carbon isotopes (Δ13Ccarb-n-C19 = δ 13Ccarb − δ 13C n-C19) during the Permian–Triassic transition at Meishan, South China. The results show that kerogen carbon isotopes underwent both gradual and sharp shifts in beds 23–25 and 26–29, respectively. The differences between carbonate and organic carbon isotopes, both the Δ13Ccarb-kero and Δ13Ccarb-n-C19, which are mainly affected by CO2-fixing enzyme and pCO2, oscillated frequently during the Permian–Triassic transition. Both the variations of Δ13Ccarb-n-C19 and Δ13Ccarb-kero coupled with the alternation between cyanobacteria and green sulfur bacteria indicated by biomarkers. The episodic low values of Δ13Ccarb-n-C19 corresponded to episodic blooms of green sulfur bacteria, while the episodic high values of Δ13Ccarb-n-C19 corresponded to episodic blooms of cyanobacteria. The relationships between the variation of carbon isotopes and biota show that the microbes which flourished after the extinction of macroorganism affected the carbon isotope fractionation greatly. Combining the carbon isotope compositions and the pattern of size variation of the conodont Neogondolella, this paper supposes that anoxia of the photic zone at bed 24 was episodic and it would be caused by the degradation of terrigenous organic matters by sulfate reducing bacteria in the upper water column. Considered together with results from previous research, the high resolution variation of the biogeochemistry presents the sequence of the important geo-events during the Permian–Triassic crisis.  相似文献   

11.
We have measured the δ18O values of the major phenocrysts (olivine, clinopyroxene and plagioclase) present in lavas from Tristan da Cunha and Gough Island. These islands, which result from the same mantle plume, have enriched radiogenic isotope ratios and are, therefore, prime candidates for an oxygen isotope signature that is distinct from that of MORB. Consistent differences between the δ18O values of olivine, pyroxene and feldspar in the Gough lavas show that the phenocrysts in the mafic Gough Island lavas are in oxygen isotope equilibrium. The olivines in lavas with SiO2 <50 wt% have a mean δ18O value of 5.19‰, consistent with crystallization from a magma having the same oxygen isotope composition as MORB. Phenocrysts in all the Gough lavas show a systematic increase in δ18O value as silica content increases, which is consistent with closed-system fractional crystallization. The lack of enrichment in δ18O of the Gough magmas suggests that the mantle source contained <2% recycled sediment. In contrast, the Tristan lavas with SiO2 >48 wt% contain phenocrysts which have δ18O values that are systematically ∼0.3‰ lower than their counterparts from Gough. We suggest that the parental mafic Tristan magmas were contaminated by material from the volcanic edifice that acquired low δ18O values by interaction with water at high temperatures. The highly porphyritic SiO2-poor lavas show a negative correlation between olivine δ18O value and whole-rock silica content rather than the expected positive correlation. The minimum δ18O value occurs at an SiO2 content of about 45 wt%. Below 45 wt% SiO2, magmas evolved via a combination of assimilation, fractionational crystallization and crystal accumulation; above 45 wt% SiO2, magmas appeared to have evolved via closed-system fractional crystallization. Received: 23 November 1998 / Accepted: 27 September 1999  相似文献   

12.
Silicon is a beneficial element for many plants and is deposited in plant tissue as amorphous bio‐opal called phytoliths. The biochemical processes of silicon uptake and precipitation induce isotope fractionation: the mass‐dependent shift in the relative abundances of the stable isotopes of silicon. At the bulk scale, δ30Si ratios span from ?2 to +6‰. To further constrain these variations in situ, at the scale of individual phytolith fragments, we used femtosecond laser ablation multi‐collector inductively coupled plasma‐mass spectrometry (fsLA‐MC‐ICP‐MS). A variety of phytoliths from grasses, trees and ferns were prepared from plant tissue or extracted from soil. Good agreement between phytolith δ30Si ratios obtained by bulk solution MC‐ICP‐MS analysis and in situ isotope ratios from fsLA‐MC‐ICP‐MS validates the method. Bulk solution analyses result in at least twofold better precision for δ30Si (2s on reference materials ≤ 0.11‰) over that found for the means of in situ analyses (2s typically ≤ 0.24‰). We find that bushgrass, common reed and horsetail show large internal variations up to 2‰ in δ30Si, reflecting the various pathways of silicon from soil to deposition. Femtosecond laser ablation provides a means to identify the underlying processes involved in the formation of phytoliths using silicon isotope ratios.  相似文献   

13.
The geochemistry of the stable isotopes of silicon   总被引：1，自引：0，他引：1  
One hundred thirty two new measurements of the relative abundances of the stable isotopes of silicon in terrestrial materials are presented. The total variation of δ30Si found is 6.2%., centered on the mean of terrestrial mafic and ultramafic igneous rocks, δ30Si = ?0.4%.. Igneous rocks show limited (1.1%.) variation; coexisting minerals exhibit small, systematic silicon isotopic fractionations that are roughly 13 the magnitude of concomitant oxygen isotopic fractionations at 1150°C. In both igneous minerals and rocks, δ30Si shows a positive correlation with silicon content, as does δ18O. Opal from both sponge spicules and sinters is light, with \?gd30Si = ?2.3 and ?1.4%., respectively. Large δ30Si values of both positive and negative sign are reported for the first time from clay minerals (?2.3 to +1.8%.), opaline phytoliths (?1.4 to +2.8%.), and authigenic quartz (+ 1.4%.). All highly fractionated samples were precipitated from solution at low temperatures; however, aqueous silicon is not measurably fractionated relative to quartz at equilibrium. A kinetic isotope fractionation of ≈3.5%. is postulated to occur during the low temperature precipitation of opal and, possibly, poorly ordered phyllosilicates, with the silicate phase being enriched in 28Si. This fractionation, coupled with a Rayleigh precipitation model, is capable of explaining most non-magmatic δ30Si variations. Chert δ30Si values are largely inherited, but the primary opal δ30Si values can be modified by isotopic equilibration of silicate silicon and dissolved silicon during the transformation of opal into quartz.  相似文献   

14.
Silicon isotopes in dissolved silicic acid were measured in the upper four kilometers between 4°N and 3°S latitude at 110°W longitude in the eastern Equatorial Pacific. Silicon isotopes became progressively heavier with silicic acid depletion of surface water as expected from biological fractionation. The value of ε estimated by applying a steady-state isotope fractionation model to data from all stations between 4°N and 3°S was −0.77 ± 0.12‰ (std. err.). When the analysis was restricted to those stations whose temperature and salinity profiles indicated that they were directly influenced by upwelling of the Equatorial Undercurrent (EUC), the resulting value of ε was −1.08 ± 0.27‰ (std. err.) similar to the value established in culture studies (−1.1‰). When the non steady state Rayleigh model was applied to the same restricted data set the resulting value of ε was significantly more positive, −0.61 ± 0.16‰ (std. err.). To the extent that the equatorial system approximates a steady state these results support a value of −1.1‰ for the fractionation factor for isotopes of Si in the sea. Without the assumption of steady state the value of ε can only be constrained to be between −0.6 and −1.1‰. Silicic acid in Equatorial Pacific Deep Water below 2000 m had a near constant δ30Si of +1.32 ± 0.05‰. That value is significantly more positive than obtained for North Pacific Deep Water at similar depths at stations to the northwest of our study area (0.9-1.0‰) and it is slightly less positive than new measures of the δ30Si of silicic acid from the silicic acid plume centered over the Cascadia basin in the Northeast Pacific (Si(OH)4 > 180  μM, δ30Si = +1.46 ± 0.12‰ (SD, n = 4). We show that the data from the equator and Cascadia basin fit a general trend of increasing δ30Si(OH)4 with increasing silicic acid concentration in the deep sea, but that the isotope values from the Northeast Pacific are anomalously light. The observed level of variation in the silicon isotope composition of deep waters from this single ocean basin is considerably larger than that predicted by current models based on fractionation during opal formation with no isotope effect during dissolution. Confirmation of such high variability in deep water δ30Si(OH)4 within individual ocean basins will require reassessment of the mechanisms controlling the distribution of isotopes of silicon in the sea.  相似文献   

15.
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   

16.
Pillow basalt and chert form integral lithologies comprising many Archean greenstone belt packages. To investigate details of these lithologies in the >3.7 Ga Isua Greenstone Belt, SW Greenland, we measured silicon isotope compositions of quartz crystals, by secondary ion mass spectrometry, from a quartz‐cemented, quartz‐amygdaloidal basaltic pillow breccia, recrystallized chert and chert clasts thought to represent silica precipitation under hydrothermal conditions. The recrystallized chert, chert clasts and quartz cement have overlapping δ30Si values, while the δ30Si values of the quartz amygdules span nearly the entire range of previously published values for quartz precipitates of any age, despite amphibolite facies metamorphism. We suggest that the heterogeneity is derived from kinetic isotope fractionation during quartz precipitation under disequilibrium conditions in a hydrothermal setting, consistent with the pillow breccia origin. On the basis of the present data, we conclude that the geological context of each sample must be carefully evaluated when interpreting δ30Si values of quartz.  相似文献   

17.
The silicon isotope abundance ratios and atomic weights of NBS-28 and several other silicon isotope reference materials were determined in this study. For the calibration of the measurement procedure, two new synthetic isotope mixtures were prepared gravimetrically from highly enriched silicon isotope materials in the form of SiO2. All materials were converted into SiF4 gas and subsequently their silicon isotope ratios were measured on the SiF3+ species by using a gas source mass spectrometer MAT-253. The calibrated isotope abundance ratios of NBS-28 are 0.0507446 (26) for 29Si/28Si and 0.0341465 (15) for 30Si/28Si. The corresponding isotopic abundances are 92.17515(28)% for f(28Si), 4.67739(24)% for f(29Si) and 3.14746(14)% for f(30Si). The silicon molar mass of NBS-28 is determined to be 28.08653(11), which is 0.001 larger than previously reported values. In the meanwhile, the 29Si/28Si and 30Si/28Si isotope abundance ratios and atomic weights of SRM-990, IRMM-017, IRMM-018, GBW-04421 and GBW-04422 are also calibrated. These new calibrated data can improve the reliability and comparability of silicon isotope results using above calibrators.  相似文献   

18.
Cu and Zn have naturally occurring non radioactive isotopes, and their isotopic systematics in a biological context are poorly understood. In this study we used double focussing mass spectroscopy to determine the ratios for these isotopes for the first time in mouse brain. The Cu and Zn isotope ratios for four strains of wild-type mice showed no significant difference (δ65Cu -0.12 to -0.78 permil; δ66Zn -0.23 to -0.48 permil). We also looked at how altering the expression of a single copper binding protein, the prion protein (PrP), alters the isotope ratios. Both knockout and overexpression of PrP had no significant effect on the ratio of Cu isotopes. Mice brains expressing mutant PrP lacking the known metal binding domain have δ65Cu isotope values of on average 0.57 permil higher than wild-type mouse brains. This implies that loss of the copper binding domain of PrP increases the level of 65Cu in the brain. δ66Zn isotope values of the transgenic mouse brains are enriched for 66Zn to the wild-type mouse brains. Here we show for the first time that the expression of a single protein can alter the partitioning of metal isotopes in mouse brains. The results imply that the expression of the prion protein can alter cellular Cu isotope content.  相似文献   

19.
We present a double-spike isotope dilution MC-ICP-MS technique for the determination of germanium (Ge) isotope fractionation. Using this technique we determined Ge isotope compositions of geothermal spring fluids, a Columbia River Basalt sample, and an in-house diatom standard. Our technique uses a 73Ge/70Ge double spike in combination with hydride generation for Ge extraction from the sample matrix. Fractionation is determined on the 74Ge/72Ge mass ratio. The double spike allows us to effectively correct analytical isotope fractionation. Our external standard reproducibility is 0.4‰ (2 SD) over the course of several months. The minimum quantity of Ge needed for isotope analysis is approximately 2 ng. Consistent with previous work on geothermal fluids, Ge in the geothermal spring samples presented here is enriched over Si as compared to low temperature weathering signatures. This observation is typically interpreted as Ge exclusion during silicate mineral precipitation (e.g., quartz). Our isotope results indicate that the analyzed high temperature fluids fractionate Ge isotopes with a range in δ74Ge between −0.4‰ and −1.4‰ relative to a Columbia River basalt. We cautiously interpret the observed fractionation as preferential removal of heavy Ge isotopes out of solution during cooling of the hydrothermal fluid and subsequent precipitation of quartz.  相似文献   

20.
The Jinman deposit is a Ag-bearing copper vein deposit located at the north margin of the Lanping-Simao back-arc basin in West Yunnan. Systematic studies of fluid inclusions and stable isotopes are presented in this paper. The filling-replacement stage and the boiling-exhalative precipitation stage of mineralization took place atT 1 = 140–280°3 andT 2 = 94–204°C under pressure of (600 – 1200) x 105 Pa. The salinity of ore-forming solutions ranges from 5 wt% –20.8 wt% (NaCl). Sulphide δ34S(CDT) values are in the range of -9.6%.– +11.03%. with a range of 22. 66%. showing an apparent “pagoda”-shaped distribution in histogram. Meanwhile, the δ34S values of the various sulphides are consistent with the characters of isotope equilibrium fractionation, i.e., δ34 SPy>δ34SCp>δ34SBn. The TS/TOC ratios of the ores are widely variable between 0.16 and 5.54 with no correlation of any kind can be established. According to the model of Ohmoto, the oxidation-reduction ratios of sulfur species in ore-forming solutions at the two mineralization stages were calculated to be R′1 = 2.16 x 10-17 and R′2 = 1.55 x 104. δ13Coo2(PDB) values obtained from fluid inclusions in calcite and quartz are between -8.12%.-3.18%., averaging -5.26%., which are comparable with the isotopic composition of mantle-derived CO2. Inclusions in quartz yield δ13CCH4 (PEB) between -32. 11%. and -22.04%. (averaging -26.69%.), similar to that of methane in modern geothermal gases. For the ore-forming solutions, δ18 OH2O (SMOW) values are between -10.57%. and +9.77%. and δDH2O (SMOW) are between -51%. and -135%. Considering the effect of isotope exchange during water-rock reactions, most of the data are plotted along or close to the line defined by the reaction of meteoric water with clastic rocks, while a small part of the points fall near the reaction line of magmatic water with clastic rocks. In δ13C vs. δ18O diagram, the ore-forming solutions are plotted for the most part into the mixing area between the meteoric fluid and the deep-seated fluid and partially on the mixing line of P = 1. This project was founded by the “Eighth Five-Year Plan Period” State Key Program (85–901) and the Open Lab. of Ore Deposit Geochemistry, Chinese Academy of Sciences.  相似文献   

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