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1.
The magnetic susceptibility anisotropy of 275 specimens comprising 38 sites from the Cambrian slate belt in North Wales was measured to determine the magnetic fabric of the slates. The susceptibility ellipsoid is oblate for all sites, and the maximum/intermediate susceptibility plane always coincides with the cleavage plane of the slates which has a Caledonian strike and is nearly vertical. The maximum axes align sub-vertically and the intermediate axes sub-horizontally, trending NE-SW. The minimum susceptibility axes are normal to this foliation plane and coincide with the poles to the slaty cleavage. The orientations of the principal susceptibility axes are found to be in excellent agreement with the orientations of the principal strain directions, determined by X-ray goniometry on one of the samples from almost all of the sites. Correlation of the magnetic susceptibility anisotropy with predicted March strains (March, 1932) shows that the principal magnitudes of susceptibility can be related to those of the strain by: (for i = 1, 2, 3. The orthogonal principal axes), where χf and χ0 are the final and initial susceptibilities along a given axis i and lf and li are final and initial axial dimensions in the same direction i of a principal strain axis. The exponent a for the North Wales slates was found to be 0.145 ± 0.005. Knowledge of such a relationship may permit rapid approximate determinations of a petrofabric in similar rocks from their magnetic fabrics. However, the exponent a will probably have to be recalibrated for each rock type.  相似文献   

2.
First phase folds F1 developed in polydeformed Ajabgarh Group rocks of Proterozoic age are studied using various geometrical methods of analysis for compatibility of homogeneous strain in both class 1–3 pairs by correlatingt′ ga/α plots with existing curves for competent layers and matchingt ga/α plots with the flattening curves for the incompetent layers. F1 folds were initiated by the process of buckling but underwent [(λ2/λ1) = 0.2 to 0.7] for competent layers andR- values of 1.1 to 5 for incompetent layers. The varying flattening is also revealed by the geometry of folds. The apparent buckle shortening of folds which ranges between 49 and 67 per cent with a majority of the folds having shortening values between 50% and 55% (exclusive of layer parallel strain) and inverse thickness method strain up to 50%. Besides flattening, the fold geometry was also modified by the pressure solution. This is borne by the presence of dark seams rich in phyllosilicates and disseminated carbonaceous material offsetting limbs of buckled quartz veins in slates  相似文献   

3.
王健  孟勇  王欣  黄洪平  傅力浦  张欣 《地质通报》2011,30(8):1233-1237
在陕西紫阳新发现一块更为完整的强壮弓笔石(Cyrtograptus robustus)化石,对其始部、主枝、幼枝、胞管等特征进行了描述和数据统计,并与国内外相似的弓笔石进行对比。该种弓笔石主枝较宽,一级幼枝发育,相邻幼枝间隔胞管数为1~7个不等,随着主枝的延伸相邻幼枝间隔胞管数增大。笔石体没有二级幼枝,胞管形态为较矮的三角形。该种化石的补充研究为C. lapworthi带的弓笔石种类和弓笔石早期发育情况的研究提供了重要的基础资料。  相似文献   

4.
In low grade, biotite-rich metasiltstones and slates from the western side of Fleurieu Peninsula, the slaty cleavage is defined by elongate deformed old biotites and by the coincident elongate dimensions and (001) planes of thin, well aligned new biotites. Histograms of frequency versus (001)-S1 angle (S1 defined by aligned thin muscovite used as the reference plane) were determined in thin section for both populations. The old biotites show a symmetrical bimodal distribution of (001) about S1, with maxima at around 20° either side ofS1. This distribution, together with the preserved intracrystalline strain, indicates that these old grains deformed largely by slip on (001) with some modification of grain boundaries by diffusive transfer. The new biotite grains are very well aligned (standard deviation 3.8°) and show no sign of mechanical deformation. They have not been mechanically rotated into alignment but must have nucleated and grown in a specific orientation. The proportion of new to old grains increases with metamorphic grade, causing a rapid strengthening of the crystallographic alignment. In slates and phyllites with similar microstructure, the mica fabric determined by X-ray texture goniometry cannot be used as a quantitative measure of the geometry and magnitude of the bulk strain, as the intensity of the crystallographic fabric will be strongly influenced by the proportion of new mica, which is itself greatly affected by the metamorphic grade during slaty cleavage formation.  相似文献   

5.
Isotopic and chemical composition of groundwater from wells and springs, and surface water from the basalt-dominated Axum area (northern Ethiopia) provides evidence for the origin of water and dissolved species. Shallow (depth < 40 m) and deep groundwater are distinguished by both chemical and isotopic composition. Deep groundwater is significantly enriched in dissolved inorganic carbon up to 40 mmol l−1 and in concentrations of Ca2+, Mg2+, Na+ and Si(OH)4 compared to the shallow type.The δ2H and δ18O values of all solutions clearly indicate meteoric origin. Shifts from the local meteoric water line are attributed to evaporation of surface and spring water, and to strong water–rock interaction. The δ13CDIC values of shallow groundwater between −12 and −7‰ (VPDB) display the uptake of CO2 from local soil horizons, whereas δ13CDIC of deep groundwater ranges from −5 to +1‰. Considering open system conditions with respect to gaseous CO2, δ13CDIC = +1‰ of the deep groundwater with highest PCO2 = 10−0.9 atm yields δ13CCO2(gas) ≈ −5‰, which is close to the stable carbon isotopic composition of magmatic CO2. Accordingly, stable carbon isotope ratios within the above range are referred to individual proportions of CO2 from soil and magmatic origin. The uptake of magmatic CO2 results in elevated cations and Si(OH)4 concentrations. Weathering of local basalts is documented by 87Sr/86Sr ratios of the groundwater from 0.7038 to 0.7059. Highest values indicate Sr release from the basement rocks. Besides weathering of silicates, neoformation of solids has to be considered, which results in the formation of, e.g., kaolinite and montmorillonite. In several solutions supersaturation with respect to calcite is reached by outgassing of CO2 from the solution leading to secondary calcite formation.  相似文献   

6.
The variation and anisotropy in hydraulic conductivity and the coefficient of consolidation was investigated for two Swedish sulphide clays. A series of constant rate of strain oedometer tests was performed on samples trimmed in the vertical and horizontal direction. A methodology to evaluate the horizontal coefficients of consolidation c h via the horizontal hydraulic conductivity k h and the vertical compression modulus M v is proposed. Laboratory evaluations of c h are also compared with determinations of c h from in situ piezometer measurements in vertically drained sulphide clay. Furthermore, the validity of the empirical correlation between hydraulic conductivity change index C k and initial void ratio e 0, C k  = 0.5e 0 (Tavenas et al. in Can Geotech J 20(4):645–660, 1983b), was investigated for the sulphide clays. The results from the investigation show large ranges in measured hydraulic conductivities and coefficients of consolidation. However, the results indicate that the correlation C k  = 0.5e 0 is valid. The anisotropy in hydraulic conductivity and the coefficient of consolidation of the sulphide clays tested seems to be small. For design purposes, multiple tests for assessment of hydraulic conductivity and the coefficient of consolidation should be made, and a partial factor of safety, depending on the requisite level of safety and the spatial variability of the parameters, should be introduced. For design purposes in this type of clay, k h  = k v and c h  = c v are suggested.  相似文献   

7.
Diffusion coefficients for oxygen and hydrogen were determined from a series of natural uraninite-H2O experiments between 50 and 700 °C. Under hydrous conditions there are two diffusion mechanisms: (1) an initial extremely fast-path diffusion mechanism that overprinted the oxygen isotopic composition of the entire crystals regardless of temperature and (2) a slower volume-diffusive mechanism dominated by defect clusters that displace or eject nearest neighbor oxygen atoms to form two interstitial sites and two partial vacancies, and by vacancy migration. Using the volume diffusion coefficients in the temperature range of 400-600 °C, diffusion coefficients for oxygen can be represented by D = 1.90e−5 exp (−123,382 J/RT) cm2/s and for temperatures between 100 and 300 °C the diffusion coefficients can be represented by D = 1.95e−10 exp (−62484 J/RT) cm2/s, where the activation energies for uraninite are 123.4 and 62.5 kJ/mol, respectively. Hydrogen diffusion in uraninite appears to be controlled by similar mechanisms as oxygen. Using the volume diffusion coefficients for temperatures between 50 and 700 °C, diffusion coefficients for hydrogen can be represented by D = 9.28e−6 exp (−156,528 J/RT) cm2/s for temperatures between 450 and 700 °C and D = 1.39e−14 exp (−34518 J/RT) cm2/s for temperatures between 50 and 400 °C, where the activation energies for uraninite are 156.5 and 34.5 kJ/mol, respectively.Results from these new experiments have implications for isotopic exchange during natural UO2-water interactions. The exceptionally low δ18O values of natural uraninites (i.e. −32‰ to −19.5‰) from unconformity-type uranium deposits in Saskatchewan, in conjunction with theoretical and experimental uraninite-water and UO3-water fractionation factors, suggest that primary uranium mineralization is not in oxygen isotopic equilibrium with coeval clay and silicate minerals. The low δ18O values have been interpreted as resulting from the low temperature overprinting of primary uranium mineralization in the presence of relatively modern meteoric fluids having δ18O values of ca. −18‰, despite petrographic and U-Pb isotope data that indicate limited alteration. Our data show that the anomalously low oxygen isotopic composition of the uraninite from the Athabasca Basin can be due to meteoric water overprinting under reducing conditions, and meteoric water or groundwater can significantly affect the oxygen isotopic composition of spent nuclear fuel in a geologic repository, with minimal change to the chemical composition or texture. Moreover, the rather fast oxygen and hydrogen diffusion coefficients for uraninite, especially at low temperatures, suggest that oxygen and hydrogen diffusion may impart characteristic isotopic signals that can be used to track the route of fissile material.  相似文献   

8.
We report the calcite twinning strain results of a traverse across the Grenville orogen from Parry Sound, Ontario (NW) to Ft. Ann, New York (SE), including the younger, adjacent Ordovician Taconic allochthon. Fifty four carbonates (marbles, calcite veins, Ordovician limestone) were collected resulting in 68 strain analyses on mechanically twinned calcite (n = 2337 grains) across the Central Gneiss Belt (CGB; 3 samples), the Central Metasedimentary Belt (CMB; 27 samples), the Central Granulite Terrane (CGT; Adirondack's; 13 samples) and the Ottawan Orogenic Lid (OOL; 11 samples). Twinning strains in the greenschist-grade OOL marbles preserve N–S shortening and U-Pb titanite ages (～1150 Ma; n = 4) document these marbles formed during the Shawinigan (1190–1140 Ma) part of the Grenville orogen. From northwest to southeast, the Ottawan (1095–1020 Ma) twinning strain is dominantly a layer-parallel shortening fabric oriented N–S (Parry Sound), then becomes parallel to the Grenville thrust direction (NW–SE) across the CMB to the Adirondack Highlands where the sub-horizontal shortening strain becomes margin-parallel (SW–NE). Within the regional sample suite there are two areas studied in detail, the Bancroft shear zone (n = 11) and a roadcut on the southeast side of the Adirondack Mountains (Ft. Ann, NY; n = 8). Marbles from the Bancroft shear zone contain calcite grains with 2 sets of twin lamellae (e1 and e2). The better-developed e1 sets (n = 406) record a horizontal fabric oriented NW–SE whereas the younger e2 lamellae (n = 146) preserve a margin-parallel (SW–NE) horizontal fabric. Both the e1 and e2 strains record an overprint vertical shortening strain (NEV), perhaps related to extensional orogenic collapse. We also report an Ottawan orogen-aged granoblastic mylonite (1093 Ma, U-Pb zircon; 1102 Ma Ar-Ar biotite) in the Keweenaw thrust hanging wall 500 km inboard of the Grenville front and interpret the relations of Grenville-Keweenaw far-field dynamics.  相似文献   

9.
Six new heat flow determinations are presented for Proterozoic mobile belts of the Churchill Province of the Canadian Shield, an area that was affected by several stages of the Hudsonian orogenic sequence (1.9-1.6 Ga ago). With other, previously published, values the mean of eight determinations considered reliable and representative and corrected for the effects of Pleistocene glaciation is 44 ± 7 mW m−2. Heat generation measurements have also been made; values range from 0.1–1.04 μW m−3.A linear relation between heat flow and heat production is apparent. The heat flow axis intercept is 37 mW m−2, and the scale depth is 11 km, compared with 28 mW m−2 and 13.6 km for the Archaean Superior Province. Approximately 20% of the Churchill heat flow appears to be derived from radioactive decay in the upper crust, compared with 30% for the Superior Province and shields as a whole. The observations imply that the heat flow-heat production relation for the Churchill Province should be written as Q = Qc + Qe + A0b where Qc is equivalent to the reduced heat flow for the Archaean terrain, b is similar for the two, and Qe is an additional component of heat flow in the Proterozoic mobile belts of the Churchill Province.A speculative tectonic model is presented. It is suggested that rifting along two axes of an original craton, which had lateral variations in near surface radiogenic element concentration, followed by erosion of the radiogenic layer and subsequent reconvergence of the cratonic segments, led to widespread redistribution of radioactive elements into the reactivated inter-rift crustal block. One result would be that crustal temperatures are higher in that part of the Churchill Province than in the Superior.  相似文献   

10.
Diffusion parameters for HTO, 36Cl−, and 125I− were determined on Upper Toarcian argillite samples from the Tournemire Underground Research Laboratory (Aveyron, France) using the through diffusion technique. The direction of diffusion was parallel to the bedding plane. The purpose of the present study was 3-fold; it was intended (i) to confirm the I− interaction with Upper Toarcian argillite and to verify the effects of initial I− concentration on this affinity, as previously observed by means of radial diffusion experiments, (ii) to highlight any discrepancy between Cl− and I− diffusivity, and (iii) to investigate the effect of an increase of the ionic strength of the solution on the anionic tracers’ diffusive behaviour. The results show that the effective diffusion coefficient (De) and diffusion accessible porosity (εa) values obtained with an ionic strength (I.S.) synthetic pore water of 0.01 eq L−1 are: De = 2.35–2.50 × 10−11 m2 s−1 and εa = 12.0–15.0% for HTO, and De = 14.5–15.5 × 10−13 m2 s−1 and εa = 2.5–2.9% for 36Cl−. Because of anionic exclusion effects, anions diffuse slower and exhibit smaller diffusion accessible porosities than HTO, taken as a water tracer. The associated effective diffusion coefficient (De) and rock capacity factor (α) obtained for 125I are: De = 7.00–8.60 × 10−13 m2 s−1 and α = 4.3–7.2%. Such values make it possible to calculate low 125I distribution ratios (0.0057 < RD < 0.0192 mL g−1) which confirm the trend indicating that the 125I rock capacity factor increases with the decrease of the initial I− concentration. Additional through-diffusion experiments were carried out with a higher ionic strength synthetic pore water (I.S. = 0.11 eq L−1). No evolution of HTO diffusion parameters was observed. The anionic tracers’ effective diffusion coefficient increased by a factor of two but no clear evolution of their accessible porosity was observed. Such a paradox could be related to the particularly small mean pore size of the Upper Toarcian argillite of Tournemire. The most significant finding of this study is the large discrepancy (factor of two) between the values of the effective diffusion coefficient for 125I and 36Cl. Whatever the ionic strength of the synthetic solution used, 125I exhibited De values two times lower than those of 36Cl. A detailed explanation for this difference cannot be given at present even if a hypothesis based on ion-pairing or on steric-exclusion cannot be excluded. This makes questionable the assumption usually made for quantifying 125I sorption and postulating that 36Cl and 125I would diffuse in the same porosity. In other terms, at Tournemire, 125I sorption could be more pronounced than previously indicated.  相似文献   

11.
Paleo-hydrologic and -vegetation proxy data from the Tanganyika basin are integrated in energy and water balance equations to infer past evaporation and precipitation during the last glacial maximum (LGM). Our approach is first validated on the modern system. Large variations are assigned to input variables to simulate the interannual precipitation variability. Equations are then applied to the LGM. We first change those input parameters inferred from proxies (basin and lake surfaces, temperature, and land albedo). Our LGM simulation suggests (in percent of modern mean values) decreases in evaporation from the lake [El: −5% (between −13% and +3%)] and land [Ec: −8% (−19/+5)] bodies, in precipitation [P: −11% (−21/0)] and (P − Ec): −42% (−44/−40). Decreases in P and E are amplified [El: −8% (−16/0); Ec: −14% (−24/−2); P: −17% (−26/−6)] when including empirical changes in atmospheric transmission coefficient and Bowen ratio. Sensitivity runs suggest that even large changes in cloud cover and air humidity should not modify these trends. The results suggest that the Earth's glacial/interglacial boundary conditions play a significant role on climate of subequatorial southern Africa.  相似文献   

12.
Stratigraphic changes in the εNd of epeiric sea carbonates from central North America track the submergence history of the interior craton during the Late Ordovician. Fluctuations in sea level changed the Nd isotope balance of the epeiric sea by modifying the flux of Nd weathered from the highlands of the Taconic Orogen (εNd = −6 to −9) and from the low relief Precambrian basement (εNd = −22 to −15) of the Transcontinental Arch and Canadian Shield. Transgressions over the Arch and Shield, which diminished the weathering flux of Nd from the Precambrian basement, are recorded as positive shifts in the εNd profiles of carbonates. Negative εNd shifts reflect regression and reexposure of the Precambrian basement to erosion. Correlation of Upper Ordovician carbonates by use of the εNd profiles demonstrates the potential for Nd isotope stratigraphy. Comparison of stratigraphic variations in carbonate Sm/Nd ratios with sea level curves, conodont paleoecology, and the εNd profiles suggest that our observed variations in Sm/Nd ratios are related to changes in depth. Increasing Sm/Nd ratios correlate with increasing depth, whereas decreasing Sm/Nd ratios correlate with decreasing depth. This relationship between Sm/Nd ratios and depth suggests Sm/Nd profiles have potentially wide applications in understanding the paleoceanography of ancient epeiric seas.  相似文献   

13.
非等轴颗粒付林图解   总被引：3，自引：0，他引：3  
非等轴颗粒付林图解由直线a=1、b=1、a=b和曲线a2b=1、ab2=1分割成10个微区,并对应于不同的ex、ey、ez组合和应变类型。这些直线和曲线分别对应于特殊的ex、ey、ez组合和岩石应变类型。岩石的应变类型有18种。函数a.b的表征方程有4种类型,并分别表征直线a=1/k1和b=1/k2所分割的4个区间。a,b表征方程的确定取决于岩石总的变形行为。此图解可用于非等轴颗粒标志体应变测量和应变类型的确定和图示,文章给出了应用实例.   相似文献   

14.
 Synchrotron radiation S K-edge XANES spectra and unit-cell parameters are used to investigate the local electronic structure of non-stoichiometric binary and ternary Fe-Co-Ni monosulfide solid solution (mss; M0.923S, M = Fe, Co, Ni) quenched from 800 °C and low pressure. The prominent absorption edge feature of the XANES spectra represents transition of S 1s core level electrons to unoccupied S 3p σ* antibonding orbitals hybridized with empty metal 3d(eg) orbitals. There is a progressive increase in area of the edge peak from Fe0.923S to Ni0.923S and Co0.923S, which correlates with progressive decrease in c and a parameters for the NiAs-type subcell and increase in metallic character, and reflects increase in the number and availability of empty eg β orbitals and covalence of metal-S bonds. More generally, the area of the edge peak exhibits an inverse linear correlation with a, c and unit-cell volume of binary and ternary mss. This inverse linear correlation is attributed to progressive increase in covalence and M-S-M bonding interaction in the c-axis direction, through metal-S [M 3d(eg) - S 3p (or 3d)] π bonding. However, the area of the edge peak does not correlate very well with the average number of 3d electrons per metal atom in these solid solutions, showing that the absorption of synchrotron radiation reflects the local electronic structure of individual absorber atoms (i.e. the SM6 cluster), and is not a group (crystal energy band) effect. Received: 21 March 2000 / Accepted: 14 July 2000  相似文献   

15.
Major and trace elements and nitrogen were analysed in 59 Cambrian and Ordovician slates/phyllites of various lithostratigraphic levels within the Meguma Supergroup, 14 Ordovician slates/phyllites of The Ovens gold mineralisation, and 16 Ordovician slates/phyllites of the Eastville Pb-Zn-Cu mineralisation.The fixed nitrogen content and the normative Nfix/K2O ratio of muscovite separates members of the Goldenville (sandstone-greywacke-quartzite dominated) and Halifax Formation (slate-phyllite dominated). Low fixed nitrogen concentration is related to high manganese concentration. Black slates/phyllites of the saddle-reef-type Au-mineralisation in The Ovens area are characterised by high fixed nitrogen and a high normative Nfix/K2O ratio of muscovite. The nitrogen is of secondary hydrothermal origin. Therefore, it might be possible to use the fixed nitrogen as an exploration tool for black slates/phyllite hosted gold mineralisation in Nova Scotia. Mineralised slates/phyllites of the Eastville stratabound Pb-Zn mineralisation cannot be distinguished from nonmineralised time equivalent lithologies on the basis of the fixed nitrogen distribution or the Nfix/K2O ratio of muscovite.  相似文献   

16.
Sm-Nd systematics for nine whole-rock samples of hornblende norites, pyroxenites and a lamprophyre from various parts of the Cortlandt Complex were analyzed. Six of these samples from the central and eastern parts of the complex give an isochron age of 430±34 (2) Ma with an Nd value of –2.9±0.5, and the other three samples from the western part, including the lamprophyre, define a similar age of 394±33 (2) Ma but with a distinctly different Nd value of –1.4±0.4. The two different initial 143Nd/144Nd ratios corresponding to these -values are interpreted to reflect continental crustal contamination of the lamprophyric parental liquid prior to final emplacement and crystal fractionation to produce the different rock types of the complex. The intrusion age of 430 Ma for the complex clearly post-dates the major metamorphic event of the Taconic orogeny. The Nd-isotopic data also suggest a relationship between the Cortlandt Complex and a belt of lamprophyric dike rocks to the west, known as the Beemerville trend, which cuts across the metamorphic trends of the Taconic (Ratcliffe 1981).  相似文献   

17.
Solid solubility and structural phase transitions in (Ca x Sr1-x )TiOGeO4have been studied by means of in situ high temperature X-ray powder diffraction. The displacive A2/a–P21/a phase transition analogous to titanite has been followed across the solid solution. Strain analysis indicates a transition temperature of T c=594 ± 10 K for SrTiOGeO4 and the additional occurrence of an isosymmetric anomaly at T i =800 ± 25 K, in analogy to the isomorphous compound CaTiOGeO4. Lattice parameters as a function of temperature and composition have been determined by X-ray powder diffraction between room temperature and a maximum temperature of 1123 K. The e 11 and e 13 components dominate the strain tensor. All compositions across the solid solution exhibit close to tricritical phase transitions P21/a–A2/a. The critical temperature remains almost unaffected by substitution of Sr for Ca, but the magnitude of the spontaneous strain drops significantly with even small amounts of Sr present.  相似文献   

18.
Vacuum evaporation experiments with Type B CAI-like starting compositions were carried out at temperatures of 1600, 1700, 1800, and 1900 °C to determine the evaporation kinetics and evaporation coefficients of silicon and magnesium as a function of temperature as well as the kinetic isotope fractionation factor for magnesium. The vacuum evaporation kinetics of silicon and magnesium are well characterized by a relation of the form J = Joe−E/RT with Jo = 4.17 × 107 mol cm−2 s−1, E = 576 ± 36 kJ mol−1 for magnesium, Jo = 3.81 × 106 mol cm−2 s−1, E = 551 ± 63 kJ mol−1 for silicon. These rates only apply to evaporation into vacuum whereas the actual Type B CAIs were almost certainly surrounded by a finite pressure of a hydrogen-dominated gas. A more general formulation for the evaporation kinetics of silicon and magnesium from a Type B CAI-like liquid that applies equally to vacuum and conditions of finite hydrogen pressure involves combining our determinations of the evaporation coefficients for these elements as a function of temperature (γ = γ0e−E/RT with γ0 = 25.3, E = 92 ± 37 kJ mol−1 for γSi; γ0 = 143, E = 121 ± 53 kJ mol−1 for γMg) with a thermodynamic model for the saturation vapor pressures of Mg and SiO over the condensed phase. High-precision determinations of the magnesium isotopic composition of the evaporation residues from samples of different size and different evaporation temperature were made using a multicollector inductively coupled plasma mass spectrometer. The kinetic isotopic fractionation factors derived from this data set show that there is a distinct temperature effect, such that the isotopic fractionation for a given amount of magnesium evaporated is smaller at lower temperature. We did not find any significant change in the isotope fractionation factor related to sample size, which we interpret to mean that recondensation and finite chemical diffusion in the melt did not affect the isotopic fractionations. Extrapolating the magnesium kinetic isotope fractionations factors from the temperature range of our experiments to temperatures corresponding to partially molten Type B CAI compositions (1250-1400 °C) results in a value of αMg ≈ 0.991, which is significantly different from the commonly used value of .  相似文献   

19.
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20.
本文作者在内蒙古乌兰浩特北沙巴尔吐一带开展1∶5万区调时,根据岩石组合、古生物特征、沉积环境等对出露于该地区扎格斯台一带的一套黑色砂板岩进行了重新厘定。重新厘定后的林西组为一套黑色板岩、粉砂岩夹细砂岩地层组合,具陆相沉积特征。该套地层在原1∶20万区调工作中被划归索伦组(P_(1~s)),原1∶25万区调又将其划归哲斯组(P_(2~(zs))),本次将上部陆相碎屑岩部分重新厘定为上二叠统林西组。该地层的重新厘定对本区寻找烃源岩有重要的指导意义。  相似文献   

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