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1.
雷祥义 《第四纪研究》1992,12(2):128-135,194
黄土高原南部晚更新世黄土地层包括三层黄土（L11、L12、L13）和三层古土壤(S01、S02、S1),共六个层次。Q4/Q3界线划在S0/L11界面上,年龄约为10000aB.P.;Q3/Q2界线划在S1/L2界面上,年龄约为120000aB.P.。在区域上自北向南,晚更新世黄土的显微结构由微胶结结构组合逐渐过渡为半胶结结构组合,直到胶结结构组合,黄土的力学性质相应地由差变好。在剖面中自上而下,黄土的显微结构类型与其力学性质指标之间亦存在着上述变化规律。研究结果表明,黄土的显微结构类型作为评价黄土工程性质的一种简便方法大有在工程实践中推广使用的前景。  相似文献   

2.
The Fe L 2,3-edge spectra for a range of natural minerals and synthetic solid solutions have been measured using the technique of parallel electron energy-loss spectroscopy (PEELS) recorded in a transmission electron microscope (TEM). The Fe L 2,3 -edges of the minerals are characterised by two white-line features and exhibit electron energy-loss near-edge structure (ELNES) characteristic of Fe valence state. For divalent iron, the Fe L 3 -edge spectra are dominated by a sharp peak (white-line) at ca. 707.8 eV, followed by a broader and less intense peak at ca. 710.5 eV. The ELNES on the Fe L 3 -edge of trivalent iron consists of a white-line with its maximum at ca. 709.5 eV and a preceeding peak at ca. 708.0 eV. Mineral solid solutions that contain both Fe2+ and Fe3+ exhibit an Fe L 3 -edge shape that is composed of Fe L 3 -edges from the respective Fe2+- and Fe3+-bearing end members. The integral Fe L 2,3 -edge white-line intensity ratios I(L 3 )/I(L 2 ) show clear differences for Fe2+ and Fe3+. We demonstrate the feasibility of quantification of the ferrous/ferric ratio in minerals by determining the integral Fe L 2,3 -edge white-line intensity ratios I(L 3 )/I(L 2 ) as a function of the ferric iron concentration resulting in an universal curve within the experimental errors. The application of the universal curve combined with the high spatial resolution using the PEELS/TEM allows the quantification of the ferric iron concentration on a scale down to 10 nm, which is illustrated from a sample of ilmenite containing hematite exsolution lamellae that shows different Fe L 2,3 -edge shapes consistent with variations in the Fe2+-Fe3+ ratio over distances of ca. 100 nm. Received: 30 July 1997 / Revised, accepted: 26 October 1997  相似文献   

3.
Parallel electron energy-loss spectroscopy (PEELS) in a scanning transmission electron microscope (STEM) was used to record the Mn L2,3-edges from a range of natural and synthetic manganese containing materials, covering valences 0, II, III, IV and VII, with an energy resolution of ca. 0.5 eV. The Mn L2,3 electron-loss near-edge structure (ELNES) of these edges provided a sensitive fingerprint of its valence. The Mn2+ L2,3-edges show little sensitivity to the local site symmetry of the ligands surrounding the manganese. This is illustrated by comparing the Mn L2,3-edges from 4-, 6- and 8-fold coordinated Mn2+. In contrast, the Mn L3-edges from Mn3+ and Mn4+ containing minerals exhibited ELNES that are interpreted in terms of a crystal-field splitting of the 3d electrons, governed by the symmetry of the surrounding ligands. The Mn L3-edges for octahedrally coordinated Mn2+, Mn3+ and Mn4+ showed variations in their ELNES that were sensitive to the crystal-field strength. The crystal-field strength (10Dq) was measured from these edges and compared very well with published optically determined values. The magnitude of 10Dq measured from the Mn L3-edges and their O K-edge prepeaks of the manganese oxides were almost identical. This further confirms that the value of 10Dq measured at the Mn L3-edge is correct. Selected spectra are compared with theoretical 2p atomic multiplet spectra and the differences and similarities are explained in terms of the covalency and site symmetry of the manganese. The Mn L3-edges allow the valence of the manganese to be ascertained, even in multivalent state materials, and can also be used to determine 10Dq.  相似文献   

4.
The fine‐grained (4–11 μm) quartz Optically Stimulated Luminescence (OSL) dating technique was applied to the Weinan section on the southeastern Chinese Loess Plateau (CLP) with a high luminescence sampling resolution (10‐ and 20‐cm intervals). Fifty‐eight OSL ages, spanning c. 1–74 ka, were obtained for the 10‐m loess–palaeosol sequences. The reliability of the OSL dating and the constructed chronology was confirmed by comparing the OSL ages with independent dates from other studies and by correlation with palaeoclimatic time series. The closely spaced OSL ages at Weinan indicate that the mean dust accumulation rate (DAR) of L1–1 (MIS 2, 7.0±0.9 cm ka?1) is lower than those of L1–3 (MIS 4, 19.1±6.1 cm ka?1) and L1–2 (MIS 3, 16.0±0.7 cm ka?1) and that the mean DAR c. 30–20 ka ago (11.4±2.4 cm ka?1) is higher than that c. 20–10 ka ago (3.0±0.1 cm ka?1) in L1–1. The subsequent calculation of the mass accumulation rate (MAR) indicates that the MAR of L1–1 (107 g m?2 a?1) is much lower than those of L1–2 (247 g m?2 a?1) and L1–3 (307 g m?2 a?1). By comparing the mean DAR results during the Last Glacial at Weinan with those at a further six sites from other studies, we observed that the mean DAR of L1–2 is higher (lower) than that of L1–1 on the eastern (western) CLP, and that the mean DAR during MIS 2 has an evident transition from high to low at c. 20 ka on the entire CLP. Possible mechanisms for the above mean DAR changes at orbital and sub‐orbital time scales are presented.  相似文献   

5.
渤海西部海域新生代盖层特征及对油气的控制作用   总被引：1，自引：1，他引：0  
渤海西部海域新生代盖层发育情况与油气富集密切相关。利用渤西地区丰富的钻井资料、测井资料、取心分析化验资料等对研究区新生代盖层发育特征、封闭性及其对油气成藏的控制作用开展了研究。研究结果表明,该区主要发育东二段下部、明下段下部及明下段上部3套区域泥质岩盖层,东二段下部区域泥岩盖层相比于明下段两套区域泥岩盖层具有单层泥岩厚度大、色暗、质纯、高泥地比、横向分布稳定及更高成岩阶段等特点,东二段下部泥岩盖层封闭性好于明下段泥岩盖层;东二段下部区域泥岩盖层控制了油气在凹陷区域深部沙河街组、东营组的聚集成藏并决定了油气朝沙垒田古隆起上倾方向运移,明化镇组下段区域"终极盖层"与断裂共同作用控制了整个渤西地区新近系的油气富集程度;提出了"周边凹陷东二下区域泥岩盖层底面构造脊输导体系"、"凸起斜坡及内部明下段泥岩盖层、断裂‘耦合’油气输导体系"两种区域盖层控制下的油气输导模式。   相似文献   

6.
The distribution of Cd2+ in the presence of phthalic acid (H2Lp), ferrihydrite and bacteria (Comamonas spp.) was investigated in biologically active systems involving H2Lp biodegradation. Tests showed that Cd2+ sorption onto bacteria, ferrihydrite and bacteria-ferrihydrite mixture increased with pH in all systems, irrespective of H2Lp degradation or not. The use of bacterial growth medium, Bushnell Hass Broth modified for low phosphate, had negligible effect on Cd sorption. In the presence of ferrihydrite, no difference was observed between Cd2+ sorption in the ferrihydrite-live bacteria and in the ferrihydrite-dead bacteria systems as ferrihydrite proved to be the dominant sorption phase. Cadmium sorption to ferrihydrite and to bacterial cells was described using the diffuse layer model and a nonelectrostatic 4-site model, respectively, which were developed for systems lacking H2Lp degradation. For systems experiencing H2Lp degradation this modeling approach predicted the general trend of Cd2+ sorption-edge shift and gave good fits to the observed sorption data. The results obtained demonstrate that Cd2+ sorption in the biologically active system was reasonably estimated by a model developed for biologically inactive systems, although uncertainty exists due to processes involving H2Lp biodegradation products and changes in the bacterial population.  相似文献   

7.
The NaF effect on microlite solubility at 800°C and 170, 200, and 230 MPa is studied experimentally. The immiscibility boundaries and compositions of fluid phases L1 and L2 are defined in the system NaF–H2O at 800°C. It is established that microlite solubility increase in the L1 phase, as compared with a homogeneous solution, is explained by the appearance in the L1 phase of “free” HF in an amount of 0.025 ± 0.003 mol kg–1 H2O. The model of “acidification” L1 and “alkalizing” L2 is supposed.  相似文献   

8.
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9.
2p (L 2,3) X-ray absorption spectra are presented for a range of minerals to demonstrate the usefulness of L-edge spectroscopy as a symmetry- and valenceselective probe. 2p XAS provides a sensitive fingerprint of the electronic states of 3 d transition metals and can be applied to phases containing mixtures of such elements. Calculated spectra for 3d n → 2p 5 3d n+1 transitions provide a basis for the interpretation of the measured spectra. Thus, in principle, multiple valence states of a particular 3 d metal can be precisely characterized from a single L-edge spectrum. Examples of vanadium L-edge spectra are presented for a range of minerals; these complex spectra hold information concerning the presence of vanadium in multiple valence states. The Cu L-edge spectrum of sulvanite (Cu3 VS4) indicates the presence of both Cu+ and Cu2+; the V L-edge spectrum of the same sample shows that both V2+ and V5+ are present. Spectral simulations representing mixtures of Fe d 5 and Fe d 6 states are used to quantify Fe3+/∑Fe in a spinel, a glass, and an amphibole, all of which contain Fe as a major component. To illustrate the sensitivity of 2p XAS in a dilute system, the Fe L-edge spectrum of amethyst (α-SiO2: Fe) has been recorded; this spectrum shows that ～68% of the Fe in amethyst is Fe2+, and ～32% is Fe3+. Although previous studies on amethyst using other spectroscopic methods cite evidence for Fe4+, there is no indication in the L-edge spectrum for Fe4+ in amethyst. Comparison of theoretical and experimental spectra not only allows the valence states of 3 d ions to be recognised, but also provides site-symmetry information and crystal field parameters for each ion site.  相似文献   

10.
中原邙山黄土地层   总被引：15，自引：6，他引：9  
位于黄土高原与华北平原过渡带上的中原黄土地层,以邙山赵下峪剖面为其典型代表。据光释光和热释光测年及磁性地层研究结果,该剖面从邙山塬面至黄河河床出露S0-S10黄土-古土壤序列,总厚度172.1m,B/M界线记录于S8古土壤层顶部,以厚层晚更新世S1古土壤(15.7m)和巨厚L1黄土(77.3m)为其特色。赵下峪剖面上末次间冰期以来的平均沉积速率明显增大,其中以末次冰期晚冰阶L1LL1黄土的沉积速率最大,高达34.5mm/a。在邙山黄土堆积过程中,倒数第二冰期末(相当于L2顶部),约150ka B P,发生了风尘沉积速率的突变,其原因是此时黄河贯通三门峡东流,给风尘源区带来丰富的物质。同时赵下峪剖面的磁化率曲线所示,黄土-古土壤的磁化率强弱,并不简单地反映夏季风强度,也要受到沉积速率变化的影响。   相似文献   

11.
An experimental in situ microcosm study was conducted in the tropical lagoon La Mancha (Gulf of Mexico) to determine whether or not nutrient limitation occurs and to examine the direct effect of an inorganic nutrient pulse on the phytoplankton community structure. The phytoplankton community response to the addition of four treatments with different combinations of nitrogen (N), phosphorus (P), and silica (Si) (+N-NH4 +, +P-PO4 ?, +Si-SO3, and N:P16) showed that phytoplankton was N-limited as indicated by an increase in phytoplankton biomass (i.e., chlorophyll a) (range, 8–34 mg m?3) during the dry season in two consecutive years (2006 and 2007). Picophytoplankton abundance significantly increased in the +N treatment (145.46 103 cells L?1), while microphytoplankton reached a maximum abundance (68.38 103 cells L?1) in the N:P16 treatment. Phytoplankton composition changed from a community initially dominated by dinoflagellates (e.g., Prorocentrum spp.) to another dominated by diatoms (Thalassiosira and Nitzschia longissima) in the N:P16 treatment. The +N treatment significantly increased Synechococcus sp. growth rates (1.3 divisions per day) (picocyanobacteria). Biomarker pigments measured in the experimental microcosms confirmed observed changes in phytoplankton groups. Our results reveal that La Mancha lagoon is a N-limited coastal system during the dry season and provides evidence of the temporal species successional patterns and mechanisms regulating the phytoplankton community response to nutrient enrichment pulses in this already eutrophic coastal lagoon.  相似文献   

12.
The effect of the source water quality on As(V) removal by coagulation/microfiltration (C/MF) was investigated systematically using a jar test and a lab-scale test; the results of the lab-scale test coincide with those of the jar test. It showed that the increase of dissolved organic carbon (DOC), HPO4 2− and HCO3 − concentrations would moderately decrease As(V) removal, and the residual As(V) concentration in treated water is no more than 10 μg L−1 when the concentration of DOC, HPO4 2− and HCO3 − in raw water is not beyond 9.22 mg L−1, 1.6 mg L−1 and 300 mg L−1, respectively. Other co-ions, such as Cl−, NO3 −, F−, SO4 2−, and counter-ions including K+, Ca2+ and Mg2+, have little effect on As(V) removal. Both results of the jar test and the lab-scale test demonstrate that Fe3+ dose of 6 mg L−1 is enough to eliminate the influence of HCO3 − whose concentration changes from 350 mg L−1 to 450 mg L−1. In the lab-scale test, As(V) removal ranged from 92.8 to 98.2% at Fe3+ dose of 4 mg L−1 and 5 mg L−1 when As(V) concentration in raw water was about 100 μg L−1. The results obtained in this study suggest that As(V) removal by C/MF process is sensitive to the quality of raw water, and a jar test needs to be done before C/MF process is used for arsenic removal from drinking water.  相似文献   

13.
The long-term sustainability of an anaerobic ammonium oxidation (anammox) process in a moving bed biofilm reactor (MBBR) treating highly concentrated (mean of 740 mg NH4 +-N L?1) wastewater was demonstrated by 1600 days of efficient operation. A high maximum total nitrogen removal rate (TNRR) of 1.5 g N m?2 d?1 was achieved at the low temperature of 20 °C. For nitrogen removal recovery in cases of nitrite inhibition, anammox intermediate nitric oxide (NO) was tested in batch experiments as an N-removal accelerating agent. The effect of the addition of various NO dosages (8–72 mg NO-N L?1) was studied under inhibitory nitrite concentrations (>100 mg NO2 ?-N L?1) for anammox bacteria. Optimal maintained NO concentration was 58 mg NO-N L?1 and brought about the highest biofilm-specific anammox activity (SAA). Compared to a blank test, the minimum concentration of added NO of 40 mg NO-N L?1 showed a statistically significant (p < 0.05) accelerating effect on SAA. No inhibition of SAA by NO was observed, although at NO concentrations exceeding 72 mg NO-N L?1, the acceleratory effect upon SAA was decreased by 8%. Changes in the bacterial consortia involved in nitrogen conversion were determined concurrently for the different nitrogen removal rates and operational conditions. Quantities of Planctomycetales clone P4 strains, which are the closest (99% similarity) relative to Candidatus Brocadia fulgida, increased from 1 × 103 to 1 × 106 anammox gene copies per g total suspended solids during reactor operation days 568–1600, which was determined by quantitative polymerase chain reaction. During the operation of the MBBR, the abundance of ammonium-oxidizing bacteria (AOB) increased proportionally (up to 30%). The abundance of nitrite-oxidizing bacteria (NOB) did not increase (remaining below 10%) during days 232–860. AOB became predominant over NOBs owing to the inhibition of free ammonia spiking on NOBs.  相似文献   

14.
The subsurface mobility of Np is difficult to predict in part due to uncertainties associated with its sorption behavior in geologic systems. In this study, we measured Np adsorption onto a common gram-positive soil bacterium, Bacillus subtilis. We performed batch adsorption experiments with Np(V) solutions as a function of pH, from 2.5 to 8, as a function of total Np concentration from 1.29 × 10−5 M to 2.57 × 10−4 M, and as a function of ionic strength from 0.001 to 0.5 M NaClO4. Under most pH conditions, Np adsorption is reversible and exhibits an inverse relationship with ionic strength, with adsorption increasing with increasing pH. At low pH in the 0.1 M ionic strength systems, we observed irreversible adsorption, which is consistent with reduction of Np(V) to Np(IV). We model the adsorption reaction using a nonelectrostatic surface complexation approach to yield ionic strength dependent NpO2+-bacterial surface stability constants. The data require two bacterial surface complexation reactions to account for the observed adsorption behavior: R-L1− + NpO2+ ↔ R-L1-NpO2° and R-L2− + NpO2+ ↔ R-L2-NpO2°, where R represents the bacterium to which each functional group is attached, and L1 and L2 represent the first and second of four discrete site types on the bacterial surface. Stability constants (log K values) for the L1 and L2 reactions in the 0.001 M system are 2.3 ± 0.3 and 2.3 ± 0.2, and in the 0.1 M system the values are 1.7 ± 0.2 and 1.6 ± 0.2, respectively. The calculated neptunyl-bacterial surface stability constants are not consistent with values predicted using the linear free energy correlation approach from Fein et al. (2001), suggesting that possible unfavorable steric interactions and the low charge of NpO2+ affects Np-bacterial adsorption.  相似文献   

15.
Strong tectonic earthquakes within the crust always occur on already existing faults, and they have the property of a shear rupture. Such earthquakes with surface-wave magnitudes M < 7 obviously have a geometric similarity. Because of this similarity and the validity of the Gutenberg and Richter's energy—magnitude relation, the expression M = 2 log10 L + const., with L = focal length, is valid.The expression LmaxL* for the maximum focal length, is also valid if L* is the length of the rectilinear extent of the seismic line on which the maximum earthquake occurs. The bounds of L* may be given by sharp bends and/or by traversing deep faults. Thus the maximum imaginable earthquake on a seismic line with the length L* has the magnitude Mmax = 2 log10 L* + const.For the investigated region — the Alps and adjacent areas — from the data of recent and historical strong earthquakes, it follows that Mmax = 2 log10 L* + 1.7, if L* is measured in kilometres. These limiting values lie in the centre-field of the magnitude range for maximum earthquakes, published by Shebalin in 1970. By the aid of this equation it is also possible to assess the upper limiting value of the accompanying maximum scale intensity.  相似文献   

16.
PETER WIGLEY 《Sedimentology》1973,20(2):295-304
The Sr2+ content of Barbudan limestones is proportional to the aragonite content. The Sr2+ content of calcite which has replaced aragonite varies from 3000 p.p.m. in the youngest limestones to 50 p.p.m., average values are approximately 300 p.p.m. The (mSr2+/mCa2+)L ratios from well waters within the limestone fall within the predicted values assuming KSrC～0·1. The high (mSr2+/mCa)2+L ratios expected by a lower value of KSrC do not occur. The build up of (mSr2+/mCa2+)L ratios seen in waters from Barbados is not seen in the well waters from Barbuda. The Sr2+ content of calcite is generally lower than is seen in Barbados, but similar to that seen in parts of the Miami Oolite. Diagenesis of aragonite in Barbudan limestones is probably occurring in a more open system than in Barbados.  相似文献   

17.
 In order to develop a model for simulating naturally occurring chromian spinel compositions, we have processed published experimental data on chromian spinel-melt equilibrium. Out of 259 co-existing spinel-melt experiments reported in the literature, we have selected 118 compositions on the basis of run time, melt composition and experimental technique. These data cover a range of temperatures 1150–1500° C, oxygen fugacities of −13<log f O2< −0.7, and bulk compositions ranging from basalt and norite, to komatiite. Six major spinel components with Cr3+, Al3+, Ti4+, Mg2+, Fe3+ and Fe2+-bearing end-members were considered for the purpose of describing chromite saturation as a function of melt composition, temperature and oxygen fugacity at 1 atmosphere pressure (0.101 MPa). The empirically calibrated mineral-melt expression based on multiple linear regressions is: K Sp i =A/T(K)+B log f O2+C ln (Fe3+/Fe2+)L+D ln R L +E, where K Sp i is an equilibrium constant and R L is a melt structure-chemical parameter (MSCP). Twenty-eight forms of equilibrium constants were considered, including single distribution coefficients, exchange equilibrium constants, formation constants for AB2O4 components, as well as simple “spinel cation ratios”. For each form of the equilibrium constants, a set of 16 combinations of the MSCPs have been investigated. The MSCP is present in the form of composite ratios [e.g., Si/O, NBO/T,(Al+Si)/Si, or (Na+K)/Al] or as simple cation ratios (e.g., Mg/Fe2+). For the calculation of Fe3+ and Fe2+ species in silicate melts, we used existing equations, whereas the Fe3+/Fe2+ ratio of spinels was calculated from the spinel stoichiometry. The regression parameters that best repoduce the experimental data were for the following constants: (Fe3+/Fe2+) Sp , (Mg/Fe2+) Sp /(Mg/Fe2+) L , (Cr/Al) Sp / (Cr/Al) L , K FeCr2O4, and Ti Sp /Ti L . These expressions have been combined into a single program called SPINMELT, which calculates chromite crystallization temperature and composition at a given f O2 with an average accuracy of ∼10° C and 1–2 mol%. An example of the use of SPINMELT is presented for a magma parental to the Bushveld Complex. Received: 30 May 1995/Accepted: 1 November 1995  相似文献   

18.
According to the compuations results obtained by Bisikalo et al. (2013) for the gas-dynamical effect of stellar winds on exoplanet atmospheres, three types of gaseous envelopes can form around hot Jupiters: closed, quasi-closed, and open. The type of envelope that forms depends on the position of the frontal collision point (where the dynamical pressure of the wind is equal to the pressure of the surrounding atmosphere) relative to the Roche-lobe boundaries. Closed envelopes are formed around planets whose atmospheres lie completely within their Roche lobes. If the frontal collision point is located outside the Roche lobe, the atmospheric material begins to flow out through the Lagrangian points L1 and L2, which can result in the formation of quasi-closed (if the dynamical pressure of the stellar wind stops the outflow through L1) or open gaseous envelopes. The example of the typical hot Jupiter HD 209458b is considered for four sets of atmospheric parameters, to determine the mass-loss rates for the different types of envelopes arising with these parameters. The mass-loss rates based on the modeling results were estimated to be ? ≤ 109 g/s for a closed atmosphere, ? ? 3 × 109 g/s for a quasi-closed atmosphere, and ? ? 3 × 1010 g/s for an open atmosphere. The matter in the closed and quasi-closed atmospheres flows out mainly through L2, and the matter in open envelopes primarily through L1.  相似文献   

19.
INTRODUCTIONThe Sanmenxia area is located at the SE marginof the Loess Plateau,where a thick-layered loess de-posit developed(Fig.1).Previous research has al-ready been carried out on some loess stratigraphy inthe area(Teng,1988;Xie and Jiang,1987;Yue,1985,1984),which concentrated on petrostratigra-phy and magnetostratigraphy.Further environmentalinvestigation has not yet been pursued.After the ge-ological survey(Zheng et al.,1992;An et al.,1989;Ding and Liu,1989),more integrated str…  相似文献   

20.
The dissolution of well crystallized gibbsite far at from equilibrium was studied in batch and mixed flow through reactors. The dissolution experiments were carried out between pH 2 and 6 in the presence of 10 mmol L−1 citrate, at pH 2 and 3 in the presence of 10 mmol L−1 chloride, nitrate, and sulfate, and at pH 2 and 3 in the presence of 1.5 mmol L−1 silica at 20°C. The dissolution rate of gibbsite, RAl (mol m−2 s−1), increases in the order of chloride ≈ nitrate < silica < sulfate ≈ citrate. In presence of silica, sulphate, and citrate dissolution is catalysed by the formation of aluminium complexes at the gibbsite surface (pH 2 and 3). From pH 2 to 3 no effect of RAl on hydrogen activity is predicted as singly coordinated surface sites at the edges of the platy gibbsite crystals, [≡AlOH2+0.5] ≈ [≡AlOH], are almost saturated with protons. However at pH >3 dissolution is slowed by a decrease of [≡AlOH2+0.5].Gibbsite dissolution rates measured in closed and open systems were identical within the experimental and analytical uncertainty. This observation indicates that gibbsite dissolution is a surface controlled process. If dissolution of gibbsite occurs close to equilibrium RAl values may be predicted by an approximately linear function of ΔGr.  相似文献   

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