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Concepcion Jimenez-Lopez Jose M Dominguez-Vera 《Geochimica et cosmochimica acta》2003,67(9):1667-1676
Several mechanisms have been proposed to explain the interactions between proteins and mineral surfaces, among them a combination of electrostatic, stereochemical interactions and molecular recognition between the protein and the crystal surface. To identify the mechanisms of interaction in the lysozyme-calcium carbonate model system, the effect of this protein on the precipitation kinetics and morphology of calcite crystals was examined. The solution chemistry and morphology of the solid were monitored over time in a set of time-series free-drift experiments in which CaCO3 was precipitated from solution in a closed system at 25°C and 1 atm total pressure, in the presence and absence of lysozyme. The precipitation of calcite was preceded by the precipitation of a metastable phase that later dissolved and gave rise to calcite as the sole phase. With increasing lysozyme concentration, the nucleation of both the metastable phase and calcite occurred at lower Ωcalcite, indicating that lysozyme favored the nucleation of both phases. Calcite growth rate was not affected by the presence of lysozyme, at least at protein concentrations ranging from 0 mg/mL to 10 mg/mL.Lysozyme modified the habit of calcite crystals. The degree of habit modification changed with protein concentration. At lower concentrations of lysozyme, the typical rhombohedral habit of calcite crystals was modified by the expression of {110} faces, which resulted from the preferential adsorption of protein on these faces. With increasing lysozyme concentration, the growth of {110}, {100}, and finally {001} faces was sequentially inhibited. This adsorption sequence may be explained by an electrostatic interaction between lysozyme and calcite, in which the inhibition of the growth of {110}, {100}, and {001} faces could be explained by a combined effect of the density of carbonate groups in the calcite face and the specific orientation (perpendicular) of these carbonate groups with respect to the calcite surface. Overgrowth of calcite in the presence of lysozyme demonstrated that the protein favored and controlled the nucleation on the calcite substrate. Overgrowth crystals nucleated epitaxially in lines which run diagonal to rhombohedral {104} faces. 相似文献
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云南祖母绿的矿床地质及宝石学特征 总被引：4，自引：0，他引：4
云南祖母绿矿床产于寒武系变质岩中,矿体分别产于片麻岩的伟晶岩及云英岩脉中。属于典型的伟晶岩型或气成高温热液矿床。祖母绿的铬、钒来源于变质岩,而铍来源于伟晶岩。 相似文献
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Summary Childrenite and crandallite are described as two new phosphate members in the paragenesis of the Stari Trg mine which comprises vivianite, ludlamite and struvite. Crandallite crystals with very simple rhombohedral habit grow on rhombohedral carbonate and childrenite crystals. The crystal morphology of childrenite is very similar to that at described from other localities. Following forms were measured: {100}, {100}, {110}, {120}, {121}, {221} and {342}. The average chemical composition is Ch91 Eo9 (Ch-childrenite, Eo-eosphorite). Pseudo-orthorhombic unit cell dimensions were calculated: a = 10.390(4) A, b = 13.390(4) A and c = 6.920(2) A. Growth sectors and sector twins of childrenite are described.
With 4 Figures 相似文献
Childrenit und Crandallit aus der Stari Trg Grube (Trepa), Kosovo: Neue Daten
Zusammenfassung Childrenit und Crandallit werden als zwei neue Minerale der Phosphatgruppe beschrieben. Sie stammen aus der Stari Trg Grube in Paragenese mit Vivianit, Ludlamit und Struvit. Die Crandallit-Kristalle mit einfachem rhomboedrischen Habitus, wachsen rhomboedrischen Karbonat- und Childrenit-Kristallen auf. Die Kristallmorphologie von Childrenit ist, verglichen mit der aus anderen Lokalitäten, sehr einfach. Folgende Formen wurden gemessen: {100}, {010}, {110}, {120}, {121}, {221} und {342}. Die durchschnittliche chemische Zusammensetzung ist Ch(91Eo9(Ch-Childrenit, Eo Eosphorit). Eine Kalkulation der pseudo-orthorhombischen Elementarzelle ergab folgende Abmessungen: a = 10.390(4) A, b = 13.390(4) A and c = 6.920(2) A. Schließlich wird das Wachstum and die Zwillingsbildung von Childrenit beschrieben.
With 4 Figures 相似文献
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The morphological theory of Hartman and Perdok (1955, 1956) allows to deduce the character of a growth form {hkl} on the basis of structural data alone. Its application to the structure of whewellite leads to the identification of forms {100}, {010}, {021}, {011}, {12 \(\bar 1\) } and {121} which show during the growth a flat surface profile (flat forms F). These forms occur very frequently in the crystals we grew from pure aqueous solutions at supersaturation β≦1,90. Other forms, {001} and {10 \(\bar 1\) }, possibly show a double character (F or S, where S stays for related faces showing a stepped profile during the growth) according to the bonds assumed within some periodic bond chains (PBCs). Alternative ways of bonding water molecules lead to different structures of the same PBC. The different energy corresponding to these structures may explain the complex morphology of both natural and synthetic crystals grown at high β values. 相似文献
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Hydrothermal scheelite was synthesized using Na2WO4 · 2 H2O mixed with CaCl2 · H2O, CaSO4 · 2 H2O or CaF2 at different temperatures (270–720° C) and 108 Pa. The morphology of the crystals depends on the starting products. The observed faces include the {112}, {114}, {011}, and {013} forms. Pure or REE doped scheelites were studied by thermoluminescence (TL), fluorescence and electron paramagnetic resonance (EPR). The main TL peaks are located near 88, 149, 216, 277, and 315 K. Results obtained with EPR or optical fluorescence have been correlated with TL measurements and show that the trivalent lanthanide elements substitute for calcium ions without site distortion. The differences in TL observed between Eu and the other doping elements are related to the greater stability of Eu2+ caused by X-irradiation. 相似文献
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Whiskers and thin platelets of pyrite have been found growing coherently on the face of small cubic pyrite crystals from the Strashimir and Gradishte hydrothermal lead-zinc deposits. The host crystals formed framboids and spheroids of macroscopic size inside large crystals of chalcopyrite from which they are separated by concentric gaps. The whiskers, one to several μm in width, are elongated along [001] and bounded by {100}, partly by {210} and {111} faces. Scanning electron microscopic (SEM) observation revealed longitudinal steps and grooves, flat rectangular pits, drop-like and elongated bulges on their side faces. High-voltage electron microscopic (HVEM) studies showed that the thin whiskers are perfect and dislocation-free, although some ribbon-like whiskers and platelets contain internal longitudinal channels and small isometric fluid inclusions. Based on these observations, the following growth mechanism is proposed. Whiskers grow in the restricted volume of the internal cavities in chalcopyrite from stagnant solutions under a diffusion regime. The growth proceeds in two stages: (1) Initially, pyramidal “pedestals” are formed due to morphological instability of the host crystal surfaces and multiapex growth, (2) Whiskers grow rapidly by unidirectional supply of material and competition between neighbouring individual whiskers, the growth taking place at the tip by a two-dimensional nucleation mechanism. The whiskers and thin platelets are considered to be peculiar highly anisometric skeletal crystals. 相似文献
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Shyh‐Lung Hwang Pouyan Shen Hao‐Tsu Chu Tzen‐Fu Yui Yoshiyuki Iizuka Hans‐Peter Schertl 《Journal of Metamorphic Geology》2019,37(8):1079-1098
Metamorphic garnet commonly contains needle‐like rutile inclusions as well as equant rutile inclusions that surround quartz inclusions and range in size from submicrometer to nanometer. Although the origin of these equant rutile inclusions, that is, exsolution or non‐exsolution, has important implications for petrological and tectonic processes, the crystallographic characteristics of these inclusions have rarely been studied because of the small sizes and analytical difficulties involved. Here, we report the crystallographic characteristics pertinent to the genetic origin of minute equant rutile inclusions in cloudy, nearly spherically shaped garnet domains with Ti‐depleted compositions surrounding quartz inclusions in ultrahigh‐pressure garnet from several diamondiferous Erzgebirge quartzofeldspathic gneissic rock samples. TEM analyses show that the equant rutile crystals in cloudy garnet domains are partially bounded by the low‐energy {100}rt ± {110}rt ± {101}rt facets and have rather random crystallographic orientation relationships (CORs) with the garnet host, with preferential alignment of low‐energy lattice planes, for example, {100}rt//{112}grt, for some rutile crystals. Although the rather random CORs are unlikely to be attributed to solid‐state exsolution subjected to the stringent topotactic garnet lattice constraints, the characteristic subhedral {100}rt ± {110}rt ± {101}rt crystal forms of rutile can be rationalized by a metasomatic dissolution‐reprecipitation mechanism via a fluid phase. In this scenario, the quartz+fluid inclusions in garnet were first subjected to decompression microcracking during rock exhumation, followed by dissolution of Ti‐bearing garnet matrix at the crack tips or along the crack surfaces and subsequent reprecipitation of rutile, apatite, gahnite, akdalaite, and Ti‐depleted garnet. The rapid coalescence between rutile and garnet crystals in fluid or direct attachment of rutile crystals onto the dissolving crack surfaces would then yield the rather random CORs as reported here. These results, along with previous work on rutile needles, indicate rather diverse genesis of rutile inclusions in various crystal forms, thus shedding light on the controversial exsolution origin for other inclusion suite/microstructure in minerals. 相似文献
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云南澜沧老厂花岗斑岩中锆石标型特征及地质意义 总被引：2，自引：2，他引：0
运用Pupin的锆石标型研究方法,通过对锆石晶形的鉴定和统计来探讨云南省澜沧老厂花岗斑岩的成因信息。研究表明,本区花岗斑岩中的锆石有20种亚型,主要由{110}、{100}柱面和{101}、{211}锥面构成,其中柱面以{110}最为发育,锥面{101}和{211}都发育,但{101}较{211}更为发育;T.E.T曲线比较短,且主要分布在演化趋势图的右上角,表明锆石主要在低温过碱环境中形成,结晶速度较快,结晶温度范围750～600℃。锆石的结晶标型显示,本区隐伏花岗斑岩是以壳源为主的壳幔源混合成因的花岗斑岩。 相似文献
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晶体形态是描述矿物最直观的数据。本文对江西漂塘钨矿床中的５个黄玉晶体进行了晶体测量、投影、计算和实际晶体的立体图绘制，并对其形态特征进行了分析和总结。 相似文献
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Crystalline rocks from breccias of the Ries basin, Germany, contain highly deformed quartz. Various planar deformation structures could be observed and classified into five different types: (1) Decorated planar elements, (2) Non-decorated planar elements, (3) Homogeneous lamellae, (4) Filled lamellae, (5) Planar fractures. All these structures are parallel to crystallographic planes: {10¯13}, {10¯12}, {10¯11}, {0001},{11¯21}, {11¯22}, {21¯31}, {51¯61}, {10¯10}. The most typical and most abundant planar structures are decorated and nondecorated planar elements parallel to {10¯13} and {10¯12}. Planar fractures are parallel to {0001} and {10¯11} and form at lower stress levels, probably earlier than the planar elements.Quartz containing planar elements, especially of the non-decorated type, has lower density, index of refraction and birefringence than normal quartz. This quartz is apparently a mixture of an amorphous phase and crystalline quartz, the amount of which can be calculated using average density or refractive index.Comparison of planar quartz structures found in tectonites and those produced artificially under static or dynamic high pressure conditions demonstrates that Ries quartz closely resembles deformed quartz recovered from shock wave experiments. The planar structures found in Ries quartz have been formed by shock wave actions with peak pressures in the 100–400 kbar range.Planar elements are explained to be traces of gliding processes during shock loading visible due to the fact that a high pressure phase (stishovite and/or a stishovite-like glass phase) has been produced along the glide planes. Upon pressure release most of the high pressure phase was transformed into an SiO2-glass (diaplectic glass).In comparison with experimental data the amount of residual crystalline quartz as well as type and orientation of planar structures in the quartz grains are clues to estimate the peak pressures responsible for these deformations. Shock waves with peak pressures exceeding about 400 kbar completely transform quartz into diaplectic SiO2-glass. 相似文献
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黄铁矿成因形态学 总被引：25，自引：5，他引：20
在1981—1986年野外工作的基础上,作者对胶东三县四个金矿床黄铁矿晶体形态进行了系统研究,对其中2495粒晶体进行了统计,对300粒晶体进行了测角,对60粒晶体进行了微形貌观察。根据以上实际工作及国内外有关资料提出了黄铁矿晶休常见单形出现频率的定量资料与晶体微形貌的特点,特别是{210}面上负条纹的特征与成因探讨。并讨论了黄铁矿晶体形态与分带性,与形成温度,与主、微量成分,与共生组合及与矿化等的关系。查明黄铁矿形态及其晶面微形貌的发育与硫逸度、温度、冷却速度等密切相关。在以上基础上提出了胶东四个金矿床中蚀变岩型金矿及石英脉型金矿两种成因类型黄铁矿形态特征上的五点差异。最后对黄铁矿研究方法要点进行了总结。 相似文献
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M. Alfredsson J. P. Brodholt D. P. Dobson A. R. Oganov C. R. A. Catlow S. C. Parker G. D. Price 《Physics and Chemistry of Minerals》2005,31(10):671-682
Orthorhombic MgSiO3 perovskite is thought to be the most abundant mineral in the mantle of the Earth. Its bulk properties have been widely studied, but many geophysical and rheological processes are also likely to depend upon its surface and grain boundary properties. As a first step towards modelling these geophysical properties, we present here an investigation of the structures and energetics of the surfaces of MgSiO3-perovskite, employing both shell-model atomistic effective-potential simulations, and density-functional-theory (DFT) calculations. Our shell-model calculations predict the {001} surfaces to be the energetically most stable surfaces: the calculated value of the surface energy being 2.2 J/m2 for the MgO-terminated surface, which is favoured over the SiO2-terminated surface (2.7 J/m2). Also for the polar surfaces {111}, {101} and {011} the MgO-terminated surfaces are energetically more stable than the Si-terminated surfaces. In addition we report the predicted morphology of the MgSiO3 perovskite structure, which is dominated by the energetically most stable {001} and {110} surfaces, and which appears to agree well with the shape of grown single crystals. 相似文献
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Frequency distributions of true interfacial angles in high-grade,regional metamorphic rocks from Broken Hill indicate that interfacialtension varies with relative crystallographic orientation incommon minerals. In some single-phase aggregates (e.g. quartz,feldspar, garnet, and calcite) the grains are equant and polygonal,anisotropy of interfacial tension having only a small effecton the appearance of such aggregates. This is also true of two-phaseaggregates of these phases, but their appearance is complicatedby the presence of inclusions, the relative proportions of ihephases, and the characteristic dihedral angle formed by a grainof one phase in contact with two grains of the other. In phases for which interfacial tension is more orientation-dependent,crystal forms exert some control on the appearance of the microstructure.For example, in hornblende and pyroxene aggregates, some interfacesare parallel to planes of the form {110}, although most areirrational. In still more anisotropic phases, low-energy forms(e.g. {001} of biotite and {110} of sillimanite) are very stable,giving rise to a predominance of planar, rational boundariesover curved, adjustment boundaries. Anisotropy of interfacial tension is expressed in the shapesof inclusions. However, even where strongly anisotropic mineralsare involved, inclusions with partly planar boundaries occuralongside inclusions with completely curved boundaries. 相似文献
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Transmission electron microscopy (TEM) has been used to investigate deformation microstructures of synthetic stishovite specimens deformed at 14 GPa, 1,300°C. Geometrical characteristics of numerous dislocations have been characterized by dislocation contrast and stereographic analyses in order to identify the easy slip systems of stishovite. TEM data allowed us to characterize the following slip systems: 〈100〉{001}, 〈100〉{010}, 〈100〉{021}, [001]{100}, [001]{110}, [001]{210} and
Observation of sub-grain boundaries and scalloped edge dislocations suggest that climb has been activated in the specimens. 相似文献
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淡红沸石(Stellerite)是辉沸石族矿物之一种,曾在白令海峡中的苏联铜岛、美国阿拉斯加的朱诺、芬兰和苏联东外贝加尔的一些多金属矿床发现过。前人对淡红沸石着重进行了结晶学和热分析的研究,而对其地质产状和成因以及与有关矿化的关系相对少一些。到目前为止,我国还沒有对淡红沸石进行过报导。 相似文献
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Gerhard Vavra 《Contributions to Mineralogy and Petrology》1994,117(4):331-344
The internal morphologies of zircon crystals from different types of granitoids (alkaline, calcalkaline and anatectic) are revealed by cathodoluminescence imaging and are described in terms of growth rates of the crystal faces relative to each other. Zircons in the alkaline granitoids are characterized by high and constant growth rates of {010} relative to the pyramidal forms and by symmetric grwoth of {011}. Zircons in the calcalkaline and anatectic granitoids are characterized by fluctuating or gradually decreasing relative growth rates of {010}, by asymmetric and highly variable growth of {011}, and by a tendency of {110} to become grwoth-inhibited. Corrosion events are interspersed during zircon growth in the calcalkaline magmas. In the calcalkaline and anatectic magmas, a discontinuity breaks the morphological evolution at late stages of crystallization. The discontinuity coincides with a sharp drop in cathodoluminescence. The growth behaviour of each crystal form is analysed and compared with predictions made by the periodic bond chain (PBC) theory. It is argued that the relative growth rate of {010} depends on supersaturation, that the growth rates of {011} faces are changed in response to different ratios of adsorbing cations (Na, K, Al), and that {110} faces become growth-inhibited by the adsorption of H2O or trace elements enriched in the residual liquid. Morphological and chemical discontinuities at late stages of crystallization are reasonably explained by the formation of larger growth units (from smaller ionic entities) in the residual liquid. Important factors controlling the zircon morphology in different types of granitoids are: high cooling rates (alkaline magmas), magma mixing (calcalkaline magmas), enrichment of H2O and trace elements in residual liquids (calcalkaline and anatectic magmas), and the major element chemistry of the magma, possibly the ratio of Na and K to Al (agpaicity). 相似文献
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板状绿柱石产于花岗岩云英岩化边部或晶洞壁的白云母-钠长石-绿柱石-水晶的矿物组合中,钠长石呈自形晶,绿柱石的洁净度与透明度相对较差。晶体测量表明,晶体的单形晶面发育依次为c{0001}→s{11 2-1}→p{10 1-1}→m{10 1-0}→v{21 3-1}、n{45 9-4}、a{11 2-0}。微分干涉显微镜(DIC)及扫描电镜(SEM)研究表明:各单形晶面上生长纹(微形貌)反映面网结构的对称性,c{0001}单形晶面上的六边形溶蚀坑(50～170μm)是由平行晶体C轴的各单形晶面生长层从晶体中心向外叠堆组成,层生长机理制约晶体生长全过程,平行双面(c)的生长层较薄(5～8μm)且较稳定,六方双锥(s)生长层较厚且圆滑,六方柱(m)生长层由晶体中心往外其厚度由厚逐渐变薄(12～20μm),台间隔由窄变宽。晶体溶蚀是从面网密度最大的c{0001}开始,溶蚀面积依平行双面(c)、六方双锥(s)单形晶面由大变小,六方柱(a)、复六方双锥(v、n)单形晶面因面网密度小而未受到溶蚀。据矿物共生组合、流体包裹体均一法测量与拉曼光谱(LRS)分析表明板状绿柱石是在中–高温(303℃)、过饱和度较大、成矿介质的钠长石化发育且热动力环境相对稳定的条件下形成,气液包裹体主要由H2O、CO2及微量CH4、N2组成,CO2及微量CH4、N2可能与碳酸盐围岩有关。 相似文献
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