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1.
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   

2.
The results of the investigations of the transformation of impurity defects in natural diamonds of various habits at the stage of high-temperature annealing at P = 6 GPa and T = 2200°C are presented. The studies conducted allowed us to ascertain that the transformations of Aand B-defects in diamonds of octahedral and cubic habits follow general regularities. This fact shows that most of the diamonds of cubic habit with low degree of aggregation of nitrogen centers were not really annealed over a long-term interval. Unlike octahedral diamonds, those of cubic habit are characterized by a pronounced increase in the peak of H-containing defects (3107 cm–1) after annealing.  相似文献   

3.
ABSTRACT

The preservation of metastable diamond in ultrahigh-pressure metamorphic (UHPM) complexes challenges our understanding of the processes taking place during exhumation of these subduction zone complexes. The presence of diamonds in UHPM rocks implies that diamonds remained metastable during exhumation, and within thermodynamic stability of graphite for an extended period. This work studies the influence of pressure on the surface graphitization rate of diamond monocrystals in carbonate systems to understand the preservation of microdiamond during exhumation of UHP subduction complexes. Experiments were performed with 2–3 mm synthetic diamond monocrystals at 2–4 GPa in СаСО3 (1550°С) and К2СО3 (1450°С) melts using a high-pressure multi-anvil apparatus. The highest rate of surface graphitization took place at 2 GPa; diamond crystals were almost completely enveloped by a graphite coating. At 4 GPa, only octahedron-shaped pits formed on flat {111} diamond crystal faces. Our results demonstrate that the surface graphitization rate of diamonds in the presence of carbonate melts at 1450–1550°C increases with decreasing pressure. Decreased pressure alone can graphitize diamond regardless of exhumation rate. Metastable diamond inclusions survive exhumation with little or no graphitization because of excess pressure up to 2 GPa acting on them, and because inclusions are protected from interaction with C-O-H fluid.  相似文献   

4.

The first studies of diamonds in eclogitic xenoliths from the Komsomolskaya kimberlite pipe are described. Among round and oval-shaped xenoliths with diamond ingrowths, samples with a garnet content of 40–90% of the xenolith volume dominate. Two eclogite samples contain grains of accessory rutile; a kyanite sample is also revealed. Certain samples contain two or more crystals of diamonds. Diamonds with an octahedral habit and crystals with transitional habits, which belong to an octahedral-rhombic dodecahedral row, dominate in eclogites; there are many variety VIII aggregates. A high concentration of structural nitrogen, commonly in the A form, was registered in most of the crystals. Diamonds with a small content of nitrogen impurities, 40–67% in the B1 form, are present in a number of xenoliths. The calculated temperatures of the formation of eclogitic xenoliths is 1100–1300°C. Diversity in the impurity compositions of diamonds in the same xenolith shows that these diamonds were formed at various times and in different settings. The diamond position in xenoliths, the various level of nitrogen aggregation in the diamonds, and a number of other factors point to the later formation of the diamonds, as compared to minerals of eclogites, from fluid or fluid-melts in the process of metasomatosis.

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5.
Doklady Earth Sciences - Experimental results on the growth of cubic diamond on lonsdaleite-bearing diamonds from the Popigai astrobleme at 5.5 GPa and 1450°C in the Fe–Ni–C system...  相似文献   

6.
The internal structure of variety III diamonds (Orlov 1977) was examined by X-ray section topography. The crystal space was found to be divided into six cubic sectors of a face-form of rhombododecahedroid variety III (Shafranovsky 1961). The defect lines on the topographs are the traces of {110} defect planes. It is concluded that separate 〈111〉 fibres are grouped into {110} layers (lamellae). The internal structure of the crystals is characterized by continuous warping of crystal planes and is directly connected with {110} defect planes which are tilt boundaries. Examples of variants of filling cubic sectors are given and their connection with misorientation shown on topographs demonstrated. The characteristic internal structure of variety III diamonds can account for their morphological features and structure-dependent properties; for examples, the cleavage on {110} and {100}.  相似文献   

7.
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   

8.
Regularly oriented orthopyroxene (opx) and forsterite (fo) inclusions occur as opx + rutile (rt) or fo + rt inclusion domains in garnet (grt) from Otrøy peridotite. Electron diffraction characterization shows that forsterite inclusions do not have any specific crystallographic orientation relationships (COR) with the garnet host. In contrast, orthopyroxene inclusions have two sets of COR, that is, COR‐I: <111>grt//<001>opx and {110}grt～//～{100}opx (～13° off) and COR‐II: <111>grt//<011>opx and {110}grt～//～{100}opx (～14° off), in four garnet grains analysed. Both variants of orthopyroxene have a blade‐like habit with one pair of broad crystal faces parallel/sub‐parallel to {110}grt plane and the long axis of the crystal, <001>opx for COR‐I and <011>opx for COR‐II, along <111>grt direction. Whereas the lack of specific COR between forsterite and garnet, along with the presence of abundant infiltrating trails/veinlets decorated by fo + rt at garnet edges, provide compelling evidence for the formation of forsterite inclusions in garnet through the sequential cleaving–infiltrating–precipitating–healing process at low temperatures, the origin of the epitaxial orthopyroxene inclusions in garnet is not so obvious. In this connection, the reported COR, the crystal habit and the crystal growth energetics of the exsolved orthopyroxene in relict majoritic garnet were reviewed/clarified. The exsolved orthopyroxene in a relict majoritic garnet follows COR‐III: {112}grt//{100}opx and <111>grt//<001>opx. Based on the detailed trace analysis on published SEM images, these exsolved orthopyroxene inclusions are shown to have the crystal habit with one pair of broad crystal faces parallel to {112}grt//{100}opx and the long crystal axis along <111>grt//<001>opx. Such a crystal habit can be rationalized by the differences in oxygen sub‐lattices of both structures and represents the energetically favoured crystal shape of orthopyroxene inclusions in garnet formed by solid‐state exsolution mechanism. Considering the very different COR, crystal habit, as well as crystal growth direction, the orthopyroxene inclusions in garnet of the present sample most likely had been formed by mechanism(s) other than solid‐state exsolution, regardless of their regularly oriented appearance in garnet and the COR specification between orthopyroxene and garnet. In fact, the crystallographic characteristics of orthopyroxene and the similar chemical compositions of garnet at opx + rt inclusion domains, fo + rt inclusion domains/trails and garnet rim suggest that the orthopyroxene inclusions in the garnet are most likely formed by similar cleaving‐infiltration process as forsterite inclusions, though probably at an earlier stage of metamorphism. This work demonstrates that the oriented inclusions in host minerals, with or without specific COR, can arise from mechanism(s) other than solid‐state exsolution. Caution is thus needed in the interpretation of such COR, so that an erroneous identification of exhumation from UHP depths would not be made.  相似文献   

9.
In this paper, we consider an ontogenic model for the formation of morphological types of growth and dissolution of cubic diamonds of variety II by Yu.L. Orlov from placers of the Anabar diamondiferous region. The following ontogenic domains of crystals and corresponding evolutionary stages of growth accompanying a general decrease in supersaturation in the crystallization medium were distinguished: microblock mosaic cuboids with defects produced by the mechanism of rotational plastic deformation–cuboids with linear translation deformations–cuboids and antiskeletal growth forms of cuboids composed of octahedral growth layers–pseudocubic growth forms of a flat-faced octahedron. The crystal morphological evolution of cuboids during the bulk dissolution of individuals in fluid-bearing melt transporting them to the surface was traced. The investigation of transitional forms of cuboid diamond dissolution showed that the final form of diamond dissolution is a rounded tetrahexahedroid independent of the combination of cuboid faces with subordinate faces of octahedron, rhombododecahedron, and tetrahexahedron observed on resorbed crystals of cubic habit. It was found that the final stages of cuboid dissolution produced disk-shaped microrelief features on the diamond surface in the form of randomly distributed ideal rounded etch pits resulting from interaction with microscopic cavitation gas bubbles released during the decompression of ascending kimberlite melt.  相似文献   

10.
At temperatures above about 1100° C degassed molten kimberlites were found to attack diamond, producing both graphite and metallic iron on the diamond surface. Using ordinary kimberlites in experiments performed at 1 Kb in a closed system, diamonds developed etch features (at temperatures above about 1000° C), consistent with attack by wet CO2, but no graphite or iron was formed on the surfaces of the diamonds.  相似文献   

11.
A San Carlos olivine polycrystal has been deformed under uppermost mantle conditions, by compression at 900 °C, at a strain rate of 1.1 × 10?5 s?1, under a confining pressure of 300 MPa, using the Paterson press. Transmission electron tomography of dislocations has been performed by scanning transmission electron microscopy, by conventional transmission electron microscopy using the weak-beam dark-field technique, associated with precession or not, in order to determine the glide planes of [001] screw dislocations. This recent technique is the most suitable one since most [001] dislocations exhibit straight screw segments due to the high lattice friction on this character at low temperature. We find that [001] dislocations glide in (100), (010) and {110} as already reported, but also more unexpectedly in {120} and {130}. We show that at 900 °C, [001] {110} glide is dominant in polycrystals. We have, however, noted and characterized numerous cross-slip events in the specimen.  相似文献   

12.
Fractionations of carbon and oxygen isotopes and magnesium between coexisting dolomite and calcite have been determined for marbles and calcareous schists of a wide variety of metamorphic environments from Vermont and the Grenville Province of Ontario. Concordant equilibrium fractionations are given by 83% of the samples. Calibration of the isotopic thermometers using the Mg-calcite solvus thermometer gave in the temperature range: 650°>T°>100°C $$ \begin{gathered} 1,000\ln \alpha _{D - Ct}^{O^{18} } = 0.45 (10^6 T^{ - 2} ) - 0.40 \hfill \\ 1,000\ln \alpha _{D - Ct}^{O^{18} } = 0.18 (10^6 T^{ - 2} ) + 0.17. \hfill \\ \end{gathered} $$ These isotopic fractionation expressions differ significantly from the experimentally derived relations, including the dolomite-Mg-calcite C13 partial exchange experiments of this study. Temperature ranges obtained for the metamorphic zones of Vermont are: chlorite zone, 210° to 295° C; biotite zone, 255° to 400° C; staurolite-kyanite zone, 110° to 550° C. In amphibolite-facies rocks the quenched partition relations can be complex. The temperature of quench or recrystallization may be as large as 400° C below the inferred metamorphic maximum. Oxygen isotope disequilibrium in high grade rocks, particularly from the Chester dome area, Vermont, is characterized by large negative δO D 18 –δO Ct 18 values. The size of the equilibrium exchange system for carbon and oxygen isotopes and magnesium is small, less than a few inches across the inferred relict bedding. This is attributed to the lack of a mobile pore fluid except in systems undergoing decarbonation. C13/C12 ratios in Grenville and Vermont marbles and O18/O16 ratios in Grenville and greenschist-facies Vermont carbonates span the range of ancient limestones. Staurolite-kyanite zone calcareous schists and marbles from the Chester dome area, Vermont are depleted in O18(δO18=12 to 20‰) due to equilibrium or disequilibrium decarbonation and some partial exchange. Extrapolation of the dolomite-calcite fractionation expressions to 20° C indicates that dolomite is enriched in O18 by about 4.9‰ and in C13 by about 2.4‰.  相似文献   

13.
《Chemical Geology》2006,225(3-4):266-277
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14.
胶东乳山金矿黄铁矿形态研究   总被引：13，自引：0，他引：13       下载免费PDF全文
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15.
Transformation Trillings in Cordierite   总被引：1，自引：0，他引：1  
ZECK  H. P. 《Journal of Petrology》1972,13(3):367-380
Cordierite sector trillings, which are found well developedin some A1-rich volcanic rocks and pelitic buchites, are thoughtto have formed initially as hexagonal high cordierite crystals.Subsequent ordering of the (Al, Si) configuration in the crystalstructure would have produced the present orthorhombic modificationand simultaneously the sector trilling, preserving in the processthe hexagonal habit of form. The predominance of the regularsixfold sector pattern in the composition plane configurationof the resulting trilling is best explained by assuming thatits formation is kinetically more advantageous than that ofother configurations because it mimics the hexagonal trend setby the initial crystal. The three orthorhombic orientations in the cordierite trillingshave parallel c-axes and each can be transformed into eitherof the other two by operation of a threefold axis (rotationthrough 120°) parallel to the common c-axis and coincidentwith the main axis of the original hexagonal form. The compositionplanes in the sector trilling pattern are shown to be essentiallyirregular in the present orthorhombic form; they do not belongto {110} or {130}. The traditional explanation that the trillings are multipletwins with repeated twin and composition planes of {110} or{130} is rejected since elementary geometrical considerationsshow that this model is only feasible if (110) (110) of orthorhombiccordierite equals 120°. X-ray work shows conclusively thatthis is not the case. In fact (110) (110) = 120° woulddefine a hexagonal symmetry.  相似文献   

16.
Hydrothermal reversal experiments have been performed on the upper pressure stability of paragonite in the temperature range 550–740 ° C. The reaction $$\begin{gathered} {\text{NaAl}}_{\text{3}} {\text{Si}}_{\text{3}} {\text{O}}_{{\text{1 0}}} ({\text{OH)}}_{\text{2}} \hfill \\ {\text{ paragonite}} \hfill \\ {\text{ = NaAlSi}}_{\text{2}} {\text{O}}_{\text{6}} + {\text{Al}}_{\text{2}} {\text{SiO}}_{\text{5}} + {\text{H}}_{\text{2}} {\text{O}} \hfill \\ {\text{ jadeite kyanite vapour}} \hfill \\ \end{gathered}$$ has been bracketed at 550 ° C, 600 ° C, 650 ° C, and 700 ° C, at pressures 24–26 kb, 24–25.5 kb, 24–25 kb, and 23–24.5 kb respectively. The reaction has a shallow negative slope (? 10 bar °C?1) and is of geobarometric significance to the stability of the eclogite assemblage, omphacite+kyanite. The experimental brackets are thermodynamically consistent with the lower pressure reversals of Chatterjee (1970, 1972), and a set of thermodynamic data is presented which satisfies all the reversal brackets for six reactions in the system Na2O-Al2O3-SiO2-H2O. The Modified Redlich Kwong equation for H2O (Holloway, 1977) predicts fugacities which are too high to satisfy the reversals of this study. The P-T stabilities of important eclogite and blueschist assemblages involving omphacite, kyanite, lawsonite, Jadeite, albite, chloritoid, and almandine with paragonite have been calculated using thermodynamic data derived from this study.  相似文献   

17.
Oxygen isotope fractionation between rutile and water   总被引：1，自引：0，他引：1  
Synthetic rutile-water fractionations (1000 ln α) at 775, 675, and 575° C were found to be ?2.8, ?3.5, and ?4.8, respectively. Partial exchange experiments with natural rutile at 575° C and with synthetic rutile at 475° C failed to yield reliable fractionations. Isotopic fractionation within the range 575–775° C may be expressed as follows: 1 $$1000\ln \alpha ({\rm T}i{\rm O}_{2 } - H_2 O) = - 4.1 \frac{{10^6 }}{{T_{k^2 } }} + 0.96$$ . Combined with previously determined quartz-water fractionations, the above data permit calibration of the quartz-rutile geothermometer: 1 $$1000\ln \alpha ({\text{S}}i{\rm O}_{2 } - Ti{\rm O}_{2 } ) = 6.6 \frac{{10^6 }}{{T_{k^2 } }} - 2.9$$ . When applied to B-type eclogites from Europe, as an example, the latter equation yields a mean equilibration temperature of 565° C.  相似文献   

18.
Precious metals accompany all types of epithermal deposits. In general, the largest of these deposits occur in intrusive or extrusive rocks of alkaline or calc-alkaline affinity. The Apigania Bay vein system and Au–Ag mineralization is hosted in Mesozoic marbles and schists, and is composed primarily of five nearly parallel, high-angle quartz veins that extend for at least 200 m. Gold–silver mineralization, in association with more than thirty ore and vein minerals, is developed in three stages and occurs at the contact of marbles and schists. Zones of epidote–chlorite–calcite and sericite–albite alteration are associated with precious metal-bearing milky and clear quartz veins. Fluid inclusion studies suggest that hydrothermal mineralization was deposited under hydrostatic pressures of ~100 bars, at temperature of 120–235°C, from low to moderate, calcium-bearing, saline fluids of 0.2 to 6.8 equiv. wt.% NaCl. Calculated isotope compositions (δ18O?=??4.7‰ to 1.7‰ and δD?=??120‰ to ?80‰) for waters in equilibrium with milky and clear quartz are consistent with mixing with dilute, low temperature meteoric ore fluids. Calculated δ 13CCO2 (0.6‰ to 1.1‰) and δ 34SH2S (?7.3 to ?0.3‰) compositions of the ore fluids indicate exchange, in an open system, with a metasedimentary source. Gold and silver deposition was associated with degassing of hydrogen due to intense uplift of the mineralizing area. The physicochemical conditions of mineralization stages I to III range between 200°C and 150°C, $f_{{\text{S}}_2 } = 10^{ - 18.1} $ to 10?16.8, $f_{{\text{O}}_2 } = 10^{ - 44.0} $ to 10?41.5, pH?=?6.9 to7.6, $f_{{\text{H}}_{\text{2}} {\text{S}}} = 10^{ - 3.4} $ to 10?2.6 and $a_{{\text{H}}_{\text{2}} {\text{S}}} = 10^{ - 2.7} $ to 10?2.6. Apigania Bay could be possibly considered the latest evolutional phase of Tinos hydrothermal system.  相似文献   

19.
A low-mature coal (Ro=0.4%, from the Manjia'er depression, Tarim Basin, China) was subjected to closed system pyrolysis, in sealed gold tubes, under isothermal temperature conditions. The carbon isotopic compositions of the pyrolyst fractions (hydrocarbon, CO2, CO, etc.) at two temperature points (350°C and 550°C) were measured. The results showed that {ie359-1} value is generally heavier at 350°C than that at 550°C, because the high abundance of CO generated at low temperature would greatly influence {ie359-2} value, and the retention time of CO in gas chromatograph is close to that of CH4. But CO is formed through chemical reaction of the oxygen-containing functional group −C=O, e.g. lactones, ketones, ether, etc. at low temperature, while CO2 comes mainly from decarboxylization. The carbon isotopic composition of coal gas from Lanzhou Coal Gas Works was definitely different from that of thermally pyrolysed products from coal. The {ie359-3} value of coal gas was abnormally heavier than {ie359-4}. At the same time, the reversed sequence ({ie359-5}) of {ie359-6} and {ie359-7} happened. The bond energy of free ions generally decides the sequence of generation of hydrocarbon fractions according to the chemical structure, whereas the stability of pyrolysate fractions and their carbon isotope fractionation are affected by the C−C bond energy. This study was supported by the National Basic Research (973) Program of China (No. 2001CB209102).  相似文献   

20.
Solubility experiments were conducted for the dissolution reaction of brucite, Mg(OH)2 (cr): Experiments were conducted from undersaturation in deionized (DI) water and 0.010–4.4 m NaCl solutions at 22.5°C. In addition, brucite solubility was measured from supersaturation in an experiment in which brucite was precipitated via dropwise addition of 0.10 m NaOH into a 0.10 m MgCl2 solution also at 22.5°C. The attainment of the reversal in equilibrium was demonstrated in this study. The solubility constant at 22.5°C at infinite dilution calculated from the experimental results from the direction of supersaturation by using the specific interaction theory (SIT) is: with a corresponding value of 17.0 ± 0.2 (2σ) when extrapolated to 25°C. The dimensionless standard chemical potential (μ°/RT) of brucite derived from the solubility data in 0.010 m to 4.4 m NaCl solutions from undersaturation extrapolated to 25°C is −335.76 ± 0.45 (2σ), with the corresponding Gibbs free energy of formation of brucite, , being −832.3 ± 1.1 (2σ) kJ mol−1. In combination with the auxiliary thermodynamic data, the is calculated to be 17.1 ± 0.2 (2σ), based on the above Gibbs free energy of formation for brucite. This study recommends an average value of 17.05 ± 0.2 in logarithmic unit as solubility constant of brucite at 25°C, according to the values from both supersaturation and undersaturation. Sandia National Laboratories is a multiprogram laboratory operated by Sandia Corporation, a Lockheed Martin Company, for the United States Department of Energy’s National Nuclear Security Administration under Contract DE-AC04-94AL85000.  相似文献   

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