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尹福光 《沉积与特提斯地质》2003,23(4):79-83
康滇地区裂谷作用已得到证实,但形成这种地堑地垒的格局有多种解释,以传统的地质力学分析为主。笔者借以热力学的自由热对流原理来加以论述：攀西巨厚的火山岩体在下覆异常地幔热作用下,发生自由热对流,引起热量散失,使地壳沉降与隆起不均衡,生成地堑地垒的格局。自由对流单元的侧向迁移,使盆地形成非对称性。 相似文献
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Thermodynamic properties of high-pressure minerals that are not recoverable from synthesis experiments by conventional quenching
methods (“unquenchable” phases) usually are calculated from equation of state data and phase diagram topologies. The present
study shows that, with cryogenic methods of recovery and sample treatment, phases with a suitable decomposition rate can be
made accessible to direct thermodynamic measurements. A set of samples of Ca(OH)2-II has been synthesized in a multianvil device and subsequently recovered by cooling the high-pressure assembly with liquid
nitrogen. Upon heating from liquid nitrogen to room temperature, the material transformed back to Ca(OH)2-I. The heat effect of this backtransformation was measured by differential scanning calorimetry. A commercial differential
scanning calorimeter (Netzsch DSC 404), modified to allow sample loading at liquid nitrogen temperature was used to heat the
material from −150 to +200 °C at rates varying between 5 and 15 °C min−1. The transformation started around −50 °C very gradually, and peaked at about 0 °C. To obtain a baseline correction, each
sample was scanned under exactly the same conditions after the backtransformation was complete. Because of the relative sluggishness,
onset and offset temperatures were not well defined as compared to fast (e.g., melting) reactions. To aid in integration,
the resulting signals were successfully fitted using a generic asymmetric peak model. The enthalpy of backtransformation was
determined to be ΔH =−10.37 ± 0.50 kJ mol−1. From previous in situ X-ray diffraction experiments, the location of the direct transformation in P-T space has been constrained to 5.7 ± 0.4 GPa at 500 °C (Kunz et al. 1996). With the reaction volume known from the same study,
and assuming that ΔC
p
of the transformation remains negligible between the conditions of our measurements and 500 °C, our result gives an estimate
of the entropy of transition and the P-T slope of the reaction curve. To a first approximation, the values ΔS = −16.00 ± 0.65 J(mol · K)−1 and dP/dT = 0.0040 ± 0.0002 GPa/K have been determined. These results need to be refined by equation of state data for Ca(OH)2-II.
Received: 30 December 1999 / Accepted: 10 April 2000 相似文献
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《Geochimica et cosmochimica acta》1999,63(19-20):2939-2955
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A detailed investigation of the protoglobigerinids from the Kimmeridgian section of the Montagne de Crussol, SE France is presented. This monotonous succession of predominantly carbonate beds represents peri-platform hemipelagic deposits, well dated by ammonites. Three species were determined in thin sections and in isolated forms after extraction by acetolysis. Favusella? parva (Kuznetsova) is the most common species occurring in almost the entire succession from the Orthosphinctes to the Beckeri zones. Favusella hoterivica (Subbotina) has been retrieved less frequently from the Platynota to the Beckeri zones, and it is its oldest occurrence. The rare Globuligerina bathoniana (Pazdrowa) occurs only in the Late Kimmeridgian. Based on our study and the review of the literature a palaeogeographical map was plotted, showing that most of the protoglobigerinid occurrences are in deep water facies of the northern margin and central part of the Tethys. These records demonstrate the presence of Globuligerina bathoniana, G. oxfordiana (Grigelis), Favusella hoterivica, F.? parva and Compactogerina stellapolaris (Grigelis) in the Kimmeridgian. 相似文献
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The Northwestern (Maghreb) boundary of the Nubia (Africa) Plate 总被引：1，自引：0，他引：1
A study of the present compressional deformation of the Northwestern (Maghreb) Nubia (Africa) margin is derived from the analysis of more than 20,000 km of seismic profiles. In the western part the compression is distributed in a large zone with on-land compression in Algeria, mainly strike-slip deformation on the Algerian margin and folds and strike-slip faulting in Eastern Spain. In the middle of the Algerian margin, around Algiers, the evidences of compression become more obvious. In this area a ridge trending N–S that is interpreted as a middle to late Miocene spreading center interacted with the transpressional margin that trends E–W. North of the location of the Boumerdes–Zemmouri earthquake the oceanic crust is deformed by blind thrusts up to 60 km from the coast. These thrusts are south dipping and with the northward dipping thrusts located onshore form a wedge that maybe a positive flower structure at a crustal scale related to the right-lateral transpression of the margin. In the eastern part of the Northwestern (Maghreb) Nubia (Africa) Deformed Belt, off eastern Algeria and Tunisia, the deformation is more intense but limited to the north by the continental slope. Large late Miocene Tortonian folds are cut by the Messinian erosional surface but the present deformation is also evident. It is suggested that the deformation with a double vergence may be followed up to the north of Sicily. After the docking (18 Ma) of the Kabylies to the Africa Plate, the crust has been thinned and the Algerian Basin opened during the middle-late Miocene with an E–W direction. From the late Miocene to the Present the margin has been rethickened by transpression and uplifted. 相似文献
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Selenium isotope fractionation during reduction by Fe(II)-Fe(III) hydroxide-sulfate (green rust) 总被引：1，自引：0，他引：1
Thomas M. Johnson 《Geochimica et cosmochimica acta》2003,67(3):413-419
We have determined the extent of Se isotope fractionation induced by reduction of selenate by sulfate interlayered green rust (GRSO4), a Fe(II)-Fe(III) hydroxide-sulfate. This compound is known to reduce selenate to Se(0), and it is the only naturally relevant abiotic selenate reduction pathway documented to date. Se reduction reactions, when they occur in nature, greatly reduce Se mobility and bioavailability. Se stable isotope analysis shows promise as an indicator of Se reduction, and Se isotope fractionation by various Se reactions must be known in order to refine this tool. We measured the increase in the 80Se/76Se ratio of dissolved selenate as lighter isotopes were preferentially consumed during reduction by GRSO4. Six different experiments that used GRSO4 made by two methods, with varying solution compositions and pH, yielded identical isotopic fractionations. Regression of all the data yielded an instantaneous isotope fractionation of 7.36 ± 0.24‰. Selenate reduction by GRSO4 induces much greater isotopic fractionation than does bacterial selenate reduction. If selenate reduction by GRSO4 occurs in nature, it may be identifiable on the basis of its relatively large isotopic fractionation. 相似文献
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Gengxin Zhang Shelly D. Kelly Kenneth M. Kemner 《Geochimica et cosmochimica acta》2009,73(12):3523-250
To assess the dynamics of microbially mediated U-clay redox reactions, we examined the reduction of iron(III)-rich nontronite NAu-2 and uranium(VI) by Shewanella oneidensis MR-1. Bioreduction experiments were conducted with combinations and varied concentrations of MR-1, nontronite, U(VI) and the electron shuttle anthraquinone-2,6-disulfonate (AQDS). Abiotic experiments were conducted to quantify U(VI) sorption to NAu-2, the reduction of U(VI) by chemically-reduced nontronite-Fe(II), and the oxidation of uraninite, U(IV)O2(s), by nontronite-Fe(III). When we incubated S. oneidensis MR-1 at lower concentration (0.5 × 108 cell mL−1) with nontronite (5.0 g L−1) and U(VI) (1.0 mM), little U(VI) reduction occurred compared to nontronite-free incubations, despite the production of abundant Fe(II). The addition of AQDS to U(VI)- and nontronite-containing incubations enhanced both U(VI) and nontronite-Fe(III) reduction. While U(VI) was completely reduced by S. oneidensis MR-1 at higher concentration (1.0 × 108 cell mL−1) in the presence of nontronite, increasing concentrations of nontronite led to progressively slower rates of U(VI) reduction. U(VI) enhanced nontronite-Fe(III) reduction and uraninite was oxidized by nontronite-Fe(III), demonstrating that U served as an effective electron shuttle from S. oneidensis MR-1 to nontronite-Fe(III). The electron-shuttling activity of U can explain the lack or delay of U(VI) reduction observed in the bulk solution. Little U(VI) reduction was observed in incubations that contained chemically-reduced nontronite-Fe(II), suggesting that biologic U(VI) reduction drove U valence cycling in these systems. Under the conditions used in these experiments, we demonstrate that iron-rich smectite may inhibit or delay U(VI) bioreduction. 相似文献
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通过对分离结晶作用和批式熔融作用Cly/Clx-Cly图解的数学分析,笔者认为,虽然ClLa/Clsm-ClLa图解在一定程度上能区分这两种不同岩浆作用过程,但是,Treuil等的解释是不完全的。直线的斜率和截距还极大地受参数Cox,Coy,Dx,Dy的影响。该图解并非总是有效。本文还给出了一般式Cly/Clx-Cly在其它方面的可能应用。 相似文献
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The major chemical components of bauxite deposits of Belgaum (76° 24′E : 15° 54′N) and Yercaud (78° 14′E : 11° 48′N) areas
have been determined. A chemical continuity between parent rocks (zone I) to bauxites (zone IV) via clay (zone II) and laterites
(zone III) clearly indicates that bauxites have been derived byin situ weathering of the respective parent rocks. 相似文献
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在山东蒙阴金伯利岩中，首次发现了沂蒙矿类质同象系列新的富Ti矿物（变）种。理想的晶体化学式可表达为：K（Ti5Fe3Cr2Mg2）12O19（简称K－Ti沂蒙矿）（Ba，K）（Ti5Fe4Mg2Cr）12O19（简称Ba－Ti沂蒙矿）从而与原来确定的沂蒙矿K（Cr5Ti3Fe2Mg2）12O19和钡钛铁铝矿（Ba，K）（Cr4Fe4Ti3Mg）12O19一起构成了金伯利岩中AM12O19磁铁铅矿型矿物的K-Cr、Ba－Cr、K-Ti、Ba-Ti四种端元类型的复杂类质同象系列。新发现的两个矿物（变）种均产出于具叶片状尖晶石出溶体的镁钛铁矿中。根据结构已知的沂蒙矿中原子的占位和配位多面体情况，分析了K－Ti，Ba－Ti沂蒙矿中各原子的占位和配位多面体，认为新发现的两个（变）种在成分上与沂蒙矿和钡钛铁铬矿有明显的区别。根据镁钛铁矿、尖晶石、沂蒙矿新（变）种、钙钛矿之间的相互关系，探讨了它们的形成环境，从而为这类矿物的地幔成因提供了直接证据。 相似文献
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本文用强功率四圆单晶衍射仪精确地修正了独居石和磷钇矿的晶体结构。独居石［Ｍｏｎａｚｉｔｅ－（Ｃｅ），ＣｅＰＯ４］属单斜晶系，ａ＝６．７８４３（１７），ｂ＝６．９８９１（１２），ｃ＝６．４５９２（１０），β＝１０３．６２６（１６）°，Ｚ＝４，空间群为Ｐ２１／ｎ。使用１１０６个［Ｆ≥３σ（Ｆ）］的独立衍射点，经多轮最小二乘法修正后，最终获得偏离因子Ｒ＝０．０６０。独居石的结构由孤立的［ＰＯ４］四面体构成，Ｃｅ位于［ＰＯ４］四面体包围之中，Ｃｅ的配位数为９，独居石的Ｃｅ—Ｏ平均键长为２．５５２，Ｐ—Ｏ平均键长为１．５２８。磷钇矿（Ｘｅｎｏｔｉｍｅ，ＹＰＯ４）属四方晶系，其晶格常数为：ａ＝６．８７９１（２４），ｃ＝６．０１４７（１９），Ｚ＝４，空间群为Ｉ４Ｉ／ａｍｄ（Ｎｏ．１４１）。使用１４２个［Ｆ≥３σ（Ｆ）］的独立衍射点，经多轮最小二乘法修正后，最终获得偏离因子Ｒ为０．０４８３。磷和氧形成四面体配位，其Ｐ—Ｏ平均键长为１．５４３；稀土钇与氧原子相连构成八次配位，其Ｙ—Ｏ平均键长为２．３３３。 相似文献