青海湖沉积物支链和环烷烃组分中C20，C25和C30高度支链类异戊二烯烯烃

在青海湖不同盐度的四孔近代沉积物岩芯（Ｑ－１６Ａ，ＱＨ，ＱＥ和ＱＧ）（图１）抽提物支链和环烷烃组分中检出了非常丰富的Ｃ₂₀，Ｃ₂₅和Ｃ₃₀高度支链类异戊二烯烯烃（ｈｉｇｈｌｙｂｒａｎｃｈｅｄｉｓｏｐｒｅｎｏｉｄａｌｋｅｎｅｓ），简称ＨＢＩ烯烃。这是在我国近代湖泊沉积物发现这类化合物的首次详细报导。由于Ｃ₂₀，Ｃ₂₅和Ｃ₃₀ＨＢＩ烯烃比正构烷烃具有较强的抵抗生物降解的能力（ＲｏｂｓｏｎａｎｄＲｏｗｌａｎｄ，１９８８ｂ），因此，它们广泛分布于各种近代环境中，如湖泊、海洋和高盐环境的近代沉积物中（ＲｏｗｌａｎｄａｎｄＲｏｂｓｏｎ，１９９０）。并且，具有１～６个双键的Ｃ₂₀，Ｃ₂₅和Ｃ₃₀烯烃经常是现代沉积物中丰富的烃类。最近在印度洋现代沉积物中又发现了一个新的具有７个双键的Ｃ₃₅ＨＢＩ烯烃（Ｈｏｅｆｓｅｔａｌ，１９９５）。全饱和的Ｃ₂₀（Ｉ，附图）、Ｃ₂₅（Ⅱ，附图）和Ｃ₃₀（Ⅲ，附图）ＨＢＩ烷烃已通过标样的合成确切地确定了它们的结构。在青海湖ＱＧ孔（尕海，咸水）和ＱＥ孔（耳海，淡水）抽提物中发现了Ｃ₂₀单烯（１号峰，图２ａ）。Ｃ₂₅烯烃（２号峰，图２ａ、２ｂ）和Ｃ₃₀烯烃（主要是３号和８号峰，图２ａ、２ｂ）存在于所有四孔沉积物中。     

C3、C4植物及其硅酸体研究的古生态意义

本文概述了C₃、C₄植物生理、生态学意义、地理分布及其相应的植物硅酸体形态,进一步讨论了C₃、C₄植物硅酸体形态在我国表层土壤中的分布规律及生态学意义。最后,对洛川黑木沟全新世黄土剖面中C₃、C₄植物硅酸体形态变化特点做了分析,表明地层中典型的C₃、C₄植物硅酸体形态,作为古植物的直接证据,可以较准确地反映古植被、古环境的变化规律。     

黄土高原地区晚中新世以来陆地植被C3/C4植物相对丰度演化研究进展

晚中新世以来陆地生态系统中C3/C4植物相对丰度的演化历史是国际地学界关心的热点问题。我国黄土高原地区也有数个剖面开展了相关的研究,然而基于土壤碳酸盐碳同位素的研究结果在C4植物扩张开始的时间、过程、区域和全球一致性、C4植物相对丰度的空间梯度等主要的地质历史事实以及该区域C4植物扩张的主要驱动因素等方面的认识均存在较大的差异,这可能表明了代用指标本身存在的问题。而来自动物化石的碳同位素研究结果与碳酸盐碳同位素研究结果同样差异比较大,认为直到第四纪时期,C4植物才成为区域植被当中一个重要组分。从代用指标可靠性以及时间分辨率2个方面考虑,建议在后续的研究工作中,大力加强有机质碳同位素方面的研究,进一步查明黄土高原地区晚中新世以来C4植物扩张的历史和可能的驱动机制。     

黄土高原西部地区末次冰期和全新世有机碳同位素变化与C3/C4植被类型转换研究

文章利用黄土高原西缘代表性的塬堡剖面有机碳同位素数据,估算了末次冰期以来地表植被中C₃/C₄植 物的相对丰度,指示出研究区域末次冰期几乎为纯粹的C₃植物,而全新世为C₃植物占优势的C₃和C₄混合植被类 型。温度是控制中国黄土高原C₄植物是否发生的关键性气候因素,末次冰期向全新世转化过程中存在的某“阈值 温度”控制了两种植被类型的存在。全新世土壤有机碳同位素偏正于末次冰期,符合前人研究得到的认识。末次 冰期间冰段(MIS3)至盛冰期,土壤有机碳同位素为偏正变化趋势,符合现代C₃植物本身随气候条件改变的碳同位 素组成变化。研究表明,利用黄土-古土壤有机碳同位素进行古气候变化研究,不能只将有机碳同位素简单的解 释为C₃/C₄植物相对丰度的变化,在单一植被类型下,还需要考虑植物本身碳同位素组成随气候条件的变化;另外, 研究还说明,我国黄土高原不同地区同时段土壤有机碳同位素值可以不同,其变化可以不具有相同的趋势,因此, 简单将有机碳同位素偏正归因于夏季风增强是值得商榷的。     

贵州石灰岩和砂岩地区C4和C3植物营养元素的化学计量对N/P比值波动的影响

陆地生态系统植物的生长受到营养元素氮(N)和磷(P)的可利用性的限制。已有的证据表明营养元素的相对丰度将控制生态系统的营养元素循环和能量流动的速度。文章提出如下假设:为了适应环境的变化,植物具有可伸缩性地调整营养元素含量的能力,也就是营养元素化学计量比值变化的能力,植物N/P比值波动的影响不仅来源于N对P的相对可利用性的变化,也来源于其他营养元素化学计量的变化,尤其是与Ca的化学计量的变化。为了验证上述假设,本研究利用3种C₄植物和11种C₃植物,研究了植物N/P化学计量比值的波动随N与Ca和P与Ca化学计量的变化模式:对C₄植物来说,N/P比值的波动主要受生物量P与Ca化学计量变化的影响;而对C₃植物来说,则同时受N与Ca和P与Ca化学计量变化的控制,它们之间的相对控制能力的大小将决定植物N/P比值波动的变化梯度,C₄植物和C₃植物的N/P比值的波动都要受土壤pH值的影响。本研究对了解物种丰度和N对P的相对可利用性、N与Ca,以及P与Ca的化学计量之间关系具有重要意义。     

李雅庄煤矿煤岩中C25、C30等无环类异戊二烯烷烃的检出及其地球化学意义

对沁水盆地李雅庄煤矿煤岩样品,进行了饱和烃生物标志化合物特征研究,检测到了丰富的无环类异戊二烯烷烃,特别是C25、C30及头—头连接的高碳数无环类异戊二烯烷烃,这些化合物被认为是甲烷菌的特征标志化合物。李雅庄煤矿煤岩沉积时为偏氧化的环境,原始环境不利于细菌发育,故检出的无环类异戊二烯烷烃应主要是成煤作用后期,煤层中甲烷菌发育的痕迹。认为李雅庄煤矿煤岩样品中丰富的、与古细菌,特别是甲烷菌有关的无环类异戊二烯烷烃化合物的检出,为该地区甲烷碳同位素组成在-56.3‰-61.7‰煤层气的次生生物成因提供了地球化学依据。      

Experimental determination of the hydrothermal solubility of ReS2 and the Re–ReO2 buffer assemblage and transport of rhenium under supercritical conditions

To understand the aqueous species important for transport of rhenium under supercritical conditions, we conducted a series of solubility experiments on the Re–ReO₂ buffer assemblage and ReS₂. In these experiments, pH was buffered by the K–feldspar–muscovite–quartz assemblage; in sulfur-free systems was buffered by the Re–ReO₂ assemblage; and and in sulfur-containing systems were buffered by the magnetite–pyrite–pyrrhotite assemblage. Our experimental studies indicate that the species ReCl₄ ⁰ is dominant at 400°C in slightly acidic to near-neutral, and chloride-rich (total chloride concentrations ranging from 0.5 to 1.0 M) environments, and ReCl₃ ⁺ may predominate at 500°C in a solution with total chloride concentrations ranging from 0.5 to 1.5 M. The results also demonstrate that the solubility of ReS₂ is about two orders of magnitude less than that of ReO₂. This finding not only suggests that ReS₂ (or a ReS₂ component in molybdenite) is the solubility-controlling phase in sulfur-containing, reducing environments but also implies that a mixing process involving an oxidized, rhenium-containing solution and a solution with reduced sulfur is one of the most effective mechanisms for deposition of rhenium. In analogy with Re, TcS₂ may be the stable Tc-bearing phase in deep geological repositories of radioactive wastes.     

云南省威信县新庄煤矿区C5煤层瓦斯地质规律研究

云南威信县新庄煤矿区多为高瓦斯及煤与瓦斯突出矿井,该矿区总体上为一向斜,发育一系列轴向NEE的次级褶曲,瓦斯含量为0.25～40.55m3/t,平均为9.10m3/t。通过对矿区地质构造、煤层厚度、煤的变质程度、顶板岩性、煤层埋深、水文地质条件等瓦斯地质因素分析,其瓦斯分布规律总体上受向斜控制,瓦斯含量在次级构造(如向斜轴部)较高,瓦斯含量等值线总体上呈NEE向展布,瓦斯含量与煤层厚度呈正相关,瓦斯含量在浅部煤层中变化大,随埋深增大趋于增高,在600m以深,瓦斯含量增加的速度减慢;从泥岩顶板-泥质灰岩顶板-粉砂岩顶板,煤层瓦斯含量依次显著降低;矿区浅部地下水活动较活跃,随深度增加,下水头压力增大,有利于瓦斯的保存和富集,区内岩溶发育但大部分位于地表,对C5煤层影响甚微。     

Thermal behavior of ferric selenite hydrates (Fe2(SeO3)3·3H2O,Fe2(SeO3)3·5H2O) and the water content in the natural ferric selenite mandarinoite

Any progress in our understanding of low-temperature mineral assemblages and of quantitative physico-chemical modeling of stability conditions of mineral phases, especially those containing toxic elements like selenium, strongly depends on the knowledge of structural and thermodynamic properties of coexisting mineral phases. Interrelation of crystal chemistry/structure and thermodynamic properties of selenium-containing minerals is not systematically studied so far and thus any essential generalization might be difficult, inaccurate or even impossible and erroneous. Disagreement even exists regarding the crystal chemistry of some natural and synthetic selenium-containing phases. Hence, a systematic study was performed by synthesizing ferric selenite hydrates and subsequent thermal analysis to examine the thermal stability of synthetic analogues of the natural hydrous ferric selenite mandarinoite and its dehydration and dissociation to unravel controversial issues regarding the crystal chemistry. Dehydration of synthesized analogues of mandarinoite starts at 56–87?°C and ends at 226–237?°C. The dehydration happens in two stages and two possible schemes of dehydration exist: (a) mandarinoite loses three molecules of water in the first stage of the dehydration (up to 180?°C) and the remaining two molecules of water will be lost in the second stage (>180?°C) or (b) four molecules of water will be lost in the first stage up to 180?°C and the last molecule of water will be lost at a temperature above 180?°C. Based on XRD measurements and thermal analyses we were able to deduce Fe₂(SeO₃)₃·(6-x)H₂O (x?=?0.0–1.0) as formula of the hydrous ferric selenite mandarinoite. The total amount of water apparently affects the crystallinity, and possibly the stability of crystals: the less the x value, the higher crystallinity could be expected.     

Thermal expansion along the NaAlSi2O6–NaFe3+Si2O6 and NaAlSi2O6–CaFe2+Si2O6 solid solutions

The high temperature volume and axial parameters for six C2/c clinopyroxenes along the NaAlSi₂O₆–NaFe³⁺Si₂O₆ and NaAlSi₂O₆–CaFe²⁺Si₂O₆ joins were determined from room T up to 800°C, using integrated diffraction profiles from in situ high temperature single crystal data collections. The thermal expansion coefficient was determined by fitting the experimental data according to the relation: ln(V/V ₀) = α(T − T ₀). The thermal expansion coefficient increases by about 15% along the jadeite–hedenbergite join, whereas it is almost constant between jadeite and aegirine. The increase is related to the Ca for Na substitution into the M2 site; the same behaviour was observed along the jadeite–diopside solid solution, which presents the same substitution at the M2 site. Strain tensor analysis shows that the major deformation with temperature occurs in all samples along the b axis; on the (010) plane the higher deformation occurs in jadeite and aegirine at a direction almost normal to the tetrahedral–octahedral planes, and in hedenbergite along the projection of the longer M2–O bonds. The orientation of the strain ellipsoid with temperature in hedenbergite is close to that observed with pressure in pyroxenes. Along the jadeite–aegirine join instead the high-temperature and high-pressure strain are differently oriented.     

C1相干算法及其在三维地震勘探解释中的应用

作者在文中详细讨论了二维和三维C1相干算法.根据三维C1相干算法的特点,结合三维地震数据体的特点,考虑到三维地震勘探在各大矿区的全面普及,针对三维地震资料开发出了一套实用的应用程序进行相干处理和解释.通过对实际三维地震资料的处理,分析结果表明,C1相干技术对三维地震资料的构造、岩性解释有明显的效果.     

Limitations on the climatic and ecological signals provided by the δC values of phytoliths from a C4 North American prairie grass

Silica phytoliths, which are deposits of opal-A that precipitate in the intra- and intercellular spaces of plant tissues during transpiration, commonly contain small amounts of occluded organic matter. In this paper, we investigate whether the δ¹³C values of phytoliths from a C₄ grass, Calamovilfa longifolia, vary in response to climatic variables that can affect the carbon-isotope composition of plant tissues. There is no significant correlation (r² < 0.3) between climate variables and the δ¹³C values of C. longifolia tissues (average δ¹³C_tissue = −13.1 ± 0.6 ‰; n = 70) across the North American prairies. However, plant tissue δ¹³C values are lower for grasses collected in populated areas where the δ¹³C value of atmospheric CO₂ is expected to be lower because of fossil fuel burning. Phytolith δ¹³C values are more variable (δ¹³C = −27.3 to −23.0‰; average = −25.1 ± 1.3‰; n = 34) and more sensitive to changes in aridity than whole tissue δ¹³C values. The strongest correlations are obtained between the δ¹³C values of stem or sheath phytoliths and humidity (r² = 0.3), latitude (r² = 0.4) and amount of precipitation (r² = 0.5). However, use of these relationships is limited by the wide spread in δ¹³C values of phytoliths from different plant tissues at the same location. We have been unable to infer any relationship between δ¹³C values of phytoliths and expected variations in the δ¹³C values of atmospheric CO₂. The C. longifolia phytoliths are depleted of ¹³C relative to tissue carbon by 10-14‰. This means that the phytoliths examined in this study have carbon isotopic compositions within the range reported previously for phytoliths from C₃ plants. This observation may further limit the usefulness of soil-phytolith assemblage δ¹³C values for identifying shifts in grassland C₃:C₄ ratios.     

Thermodynamics of iron oxides: Part III. Enthalpies of formation and stability of ferrihydrite (∼Fe(OH)3), schwertmannite (∼FeO(OH)3/4(SO4)1/8), and ε-Fe2O3

Enthalpies of formation of ferrihydrite and schwertmannite were measured by acid solution calorimetry in 5 N HCl at 298 K. The published thermodynamic data for these two phases and ε-Fe₂O₃ were evaluated, and the best thermodynamic data for the studied compounds were selected.Ferrihydrite is metastable in enthalpy with respect to α-Fe₂O₃ and liquid water by 11.5 to 14.7 kJ•mol⁻¹ at 298.15 K. The less positive enthalpy corresponds to 6-line ferrihydrite, and the higher one, indicating lesser stability, to 2-line ferrihydrite. In other words, ferrihydrite samples become more stable with increasing crystallinity. The best thermodynamic data set for ferrihydrite of composition Fe(OH)₃ was selected by using the measured enthalpies and (1) requiring ferrihydrite to be metastable with respect to fine-grained lepidocrocite; (2) requiring ferrihydrite to have entropy higher than the entropy of hypothetical, well-crystalline Fe(OH)₃; and (3) considering published estimates of solubility products of ferrihydrite. The ΔG°_f for 2-line ferrihydrite is best described by a range of −708.5±2.0 to −705.2±2.0 kJ•mol⁻¹, and ΔG°_f for 6-line ferrihydrite by −711.0±2.0 to −708.5±2.0 kJ•mol⁻¹.A published enthalpy measurement by acid calorimetry of ε-Fe₂O₃ was re-evaluated, arriving at ΔH°_f (ε-Fe₂O₃) = −798.0±6.6 kJ•mol⁻¹. The standard entropy (S°) of ε-Fe₂O₃ was considered to be equal to S° (γ-Fe₂O₃) (93.0±0.2 J•K⁻¹•mol⁻¹), giving ΔG°_f (ε-Fe₂O₃) = −717.8±6.6 kJ•mol⁻¹. ε-Fe₂O₃ thus appears to have no stability field, and it is metastable with respect to most phases in the Fe₂O₃-H₂O system which is probably the reason why this phase is rare in nature.Enthalpies of formation of two schwertmannite samples are: ΔH°_f (FeO(OH)_0.686(SO₄)_0.157•0.972H₂O) = −884.0±1.3 kJ•mol⁻¹, ΔH°_f (FeO(OH)_0.664(SO₄)_0.168•1.226H₂O) = −960.7±1.2 kJ•mol⁻¹. When combined with an entropy estimate, these data give Gibbs free energies of formation of −761.3 ± 1.3 and −823.3 ± 1.2 kJ•mol⁻¹ for the two samples, respectively. These ΔG_f° values imply that schwertmannite is thermodynamically favored over ferrihydrite over a wide range of pH (2-8) when the system contains even small concentration of sulfate. The stability relations of the two investigated samples can be replicated by schwertmannite of the “ideal” composition FeO(OH)_3/4(SO₄)_1/8 with ΔG°_f = −518.0±2.0 kJ•mol⁻¹.     

K-H3OFe3(SO4)2(OH)6铁矾的XRD研究

根据X射线衍射(XRD)分析发现: A Fe₃(SO₄)₂(OH)₆(A=K⁺、H₃O⁺)系列铁钒的XRD数据十分相近,难以用XRD区别,需通过能谱(EDS)辅助分析,才能区分此类铁矾。另外,此类铁矾的003和107面网间距d随K⁺含量增大而增大,且呈一元三次方程的关系;而033和220面网间距d随K⁺含量增大而减小,呈一元二次方程的关系。对该现象从铁矾晶体结构方面进行解释:K⁺、H₃O⁺离子位于较大空隙中,且沿着Z轴方向排列,当K⁺、H₃O⁺离子之间相互替换时,会导致该铁矾晶体结构在Z轴方向有较明显的变化。     

Biachellaite, (Na,Ca,K)8(Si6Al6O24)(SO4)2(OH)0.5 · H2O, a new mineral species of the cancrinite group

Biachellaite, a new mineral species of the cancrinite group, has been found in a volcanic ejecta in the Biachella Valley, Sacrofano Caldera, Latium region, Italy, as colorless isometric hexagonal bipyramidal-pinacoidal crystals up to 1 cm in size overgrowing the walls of cavities in a rock sample composed of sanidine, diopside, andradite, leucite and hauyne. The mineral is brittle, with perfect cleavage parallel to {10$ \bar 1 $ \bar 1 0} and imperfect cleavage or parting (?) parallel to {0001}. The Mohs hardness is 5. D_meas = 2.51(1) g/cm³ (by equilibration with heavy liquids). The densities calculated from single-crystal X-ray data and from X-ray powder data are 2.515 g/cm³ and 2.520 g/cm³, respectively. The IR spectrum demonstrates the presence of SO₄²⁻, H₂O, and absence of CO₃²⁻. Biachellaite is uniaxial, positive, ω = 1.512(1), ɛ = 1.514(1). The weight loss on ignition (vacuum, 800°C, 1 h) is 1.6(1)%. The chemical composition determined by electron microprobe is as follows, wt %: 10.06 Na₂O, 5.85 K₂O, 12.13 CaO, 26.17 Al₂O₃, 31.46 SiO₂, 12.71 SO₃, 0.45 Cl, 1.6 H₂O (by TG data), −0.10 −O=Cl₂, total is 100.33. The empirical formula (Z = 15) is (Na_3.76Ca_2.50K_1.44)_Σ7.70(Si_6.06Al_5.94O₂₄)(SO₄)_1.84Cl_0.15(OH)_0.43 · 0.81H₂O. The simplified formula is as follows: (Na,Ca,K)₈(Si₆Al₆O₂₄)(SO₄)₂(OH)_0.5 · H₂O. Biachellaite is trigonal, space group P3, a =12.913(1), c = 79.605(5) ?; V = 11495(1) ?³. The crystal structure of biachellaite is characterized by the 30-layer stacking sequence (ABCABCACACBACBACBCACBACBACBABC)_∞. The tetrahedral framework contains three types of channels composed of cages of four varieties: cancrinite, sodalite, bystrite (losod) and liottite. The strongest lines of the X-ray powder diffraction pattern [d, ? (I, %) (hkl)] are as follows: 11.07 (19) (100, 101), 6.45 (18) (110, 111), 3.720 (100) (2.1.10, 300, 301, 2.0.16, 302), 3.576 (18) (1.0.21, 2.0.17, 306), 3.300 (47) (1.0.23, 2.1.15), 3.220 (16) (2.1.16, 222). The type material of biachellaite has been deposited at the Fersman Mineralogical Museum of the Russian Academy of Sciences, Moscow, Russia, registration number 3642/1.     

轻烃中C6族组成和芴系化合物与沉积环境的关系

本文对我国8个含油气盆地40多个凝析油、轻质油样品进行了气相色谱和色谱-质谱分析研究了不同沉积环境形成的凝析油和轻质油中的C₆族组成和芳烃中芴系化合物（即芴、氧芴和硫芴）特征,探讨成气母质和沉积环境,并将其作为判识天然气成因的一种手段.     

纤钡锂石 BaMg2LiAl3[Si2O6]2（OH,F）8及其晶体结构

1974年在一水晶矿石英脉晶洞中,发现了一种含Ba、Li的硅酸盐新矿物--纤钡锂石。我们对纤钡锂石进行了光性研究、比重测定、差热及热失重分析、红外光谱分析、X射线单晶结构分析等工作,现分述如下。     

Synthesis, crystal structure and crystal chemistry of ferri-clinoholmquistite, ?Li 2Mg 3Fe 3+ 2Si 8O 22(OH) 2

This work reports the synthesis of ferri-clinoholmquistite, nominally _Li2(Mg₃Fe³⁺₂)Si₈O₂₂(OH)₂, at varying f_O2 conditions. Amphibole compositions were characterized by X-ray (powder and single-crystal) diffraction, microchemical (EMPA) and spectroscopic (FTIR, Mössbauer and Raman) techniques. Under reducing conditions ( NNO+1, where NNO = Nickel–Nickel oxide buffer), the amphibole yield is very high (>90%), but its composition, and in particular the FeO/Fe₂O₃ ratio, departs significantly from the nominal one. Under oxidizing conditions ( NNO+1.5), the amphibole yield is much lower (<60%, with Li-pyroxene abundant), but its composition is close to the ideal stoichiometry. The exchange vector of relevance for the studied system is ^M2(Mg,Fe²⁺) ^M4(Mg,Fe²⁺) ^M2Fe³⁺_–1 ^M4Li_–1, which is still rather unexplored in natural systems. Amphibole crystals of suitable size for structure refinement were obtained only at 800 °C, 0.4 GPa and NNO conditions (sample 152), and have C2/m symmetry. The X-ray powder patterns for all other samples were indexed in the same symmetry; the amphibole closest to ideal composition has a = 9.428(1) Å, b = 17.878(3) Å, c = 5.282(1) Å, = 102.06(2)°, V = 870.8(3) ų. Mössbauer spectra show that Fe³⁺ is strongly ordered at M2 in all samples, whereas Fe²⁺ is disordered over the B and C sites. FTIR analysis shows that the amount of ^CFe²⁺ increases for increasingly reducing conditions. FTIR data also provide strong evidence for slight but significant amounts of Li at the A sites.     

影响C4草本植物C/N比值变化的因素与土壤有机C积累的关系

文章对采自贵州从低海拔的东部到高海拔的西部且大致平行的石灰岩和砂岩两地带均生长的3种C₄草本植物,即巴茅(Miscanthusfloridulus)、白茅(Imperatacylindrica)和类芦(Neyraudiareynaudiana),以及相对应的土壤表层样品,进行了营养元素和C同位素组成分析;研究营养元素含量随着海拔的不同而出现的变化趋势,以及这些元素之间的相互协变作用,尤其是Ca和N之间的相互协变作用对植物的N含量、C/N比值和^δ13C值的影响,以了解植物的C/N比值(指示植物残留物质量的一种标志)与土壤有机C积累的关系。研究结果表明,植物的N含量和^δ13C值具有随海拔的上升而显著增大趋势,而植物的C/N比值在砂岩地区虽有减小的趋势,在石灰岩地带则没有。对所研究的C4草本植物来说,在土壤pH值为5.8的中性条件下显示出Ca的最大吸收,因此,Ca与其他营养元素之间的协变模式在两种土壤类型中表现出相反的倾向,并存在土壤交换性Ca的边界浓度:当土壤可交换性Ca的含量为2.24mg/g,相应土壤的pH值在5.8以下时,随着土壤可交换性Ca浓度的增大,植物的N含量上升,而植物的C/N比值会显著降低;当Ca在边界浓度以上时,随着土壤可交换性Ca浓度的增大,植物的N含量下降,而植物的C/N比值有增加的趋势。由此可见,植物残留物的N含量和C/N比值受Ca元素含量的相     

Nanoinclusions of high-pressure hydrous silicate, Mg3Si4O10(OH)2 · n H2O (10?-phase), in mantle olivine: Mechanisms of formation and transformation

The 10?-phase, Mg₃Si₄O₁₀(OH)₂ · nH₂O, where n = 0.65÷2, belongs to the group of dense hydrous magnesium silicates (DHMS), which were produced in experiments and are regarded as hypothetical mineral carriers for H₂O in the mantle. However, DHMS were almost never observed in nature. The only exception is the finding of the 10?-phase as nanoinclusions in olivines from mantle nodules in kimberlites. The inclusions with sizes of a few ten nanometers have a pseudohexagonal habit and are characterized by the presence of voids free of solids. The 10?-phase fills the equatorial parts of the inclusions, and, in the majority of inclusions, it is replaced by the low-pressure serpentine + talc assemblage. Based on the analysis of electron microscope images, a model was proposed for the solid-state formation of inclusions, the precursory material of which was transformed to the 10?-phase with the liberation of a water fluid. According to this model, the formation of hydrous nanoinclusions and their subsequent autoserpentinization occurred without the influx of H₂O from the external medium through the mobilization of intrinsic hydroxyl-bearing point defects trapped during olivine crystallization. The subsequent autoserpentinization of the inclusions occurred during decompression owing to interaction between the inclusion material and the host olivine matrix. The process was accompanied by the partial exhaustion of the fluid phase and the replacement 10?-phase + H₂O = Serp + Tc. The criterion for the credibility of the model is the conservation of the volume of material during the reaction at P = const and T = const. Original Russian Text ? N.R. Khisina, R. Wirth, 2008, published in Geokhimiya, 2008, No. 4, pp. 355–363.