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1.
D. Howell C. J. O’Neill K. J. Grant W. L. Griffin S. Y. O’Reilly N. J. Pearson R. A. Stern T. Stachel 《Contributions to Mineralogy and Petrology》2012,164(6):1011-1025
Fourier transform infrared mapping of diamonds can reveal detailed information on impurities, with a spatial context. We apply this technique, combined with in situ isotopic analysis of carbon, to the study of cuboid diamond growth in a sample that exhibits some mixed-habit growth. While there has been some uncertainty in the literature regarding sectoral differences in nitrogen aggregation and subsequent platelet development, the data from this study appear far more conclusive. We show that despite nitrogen being concentrated in octahedral sectors, there is no detectable difference in the concentration-adjusted rate of nitrogen aggregation within octahedral and cuboid sectors. However, the resultant platelet development is significantly reduced in cuboid sectors compared to contemporaneously formed octahedral sectors. This finding has significant implications for the classification of diamonds using the relationship between their platelet intensity and the absorption caused by B centres. It means that cuboid diamonds naturally fall below the linear relationship that has been termed regular, which would lead to them being incorrectly interpreted as having experienced heating or deformation. The data also support earlier suggestions that large hydrogen concentrations in the diamond-forming fluid may be required for cuboid growth. We further suggest that high nitrogen and hydrogen concentrations are required for mixed-habit diamond growth, which might be the product of specific fluid chemistries that occur in reducing mantle environments. 相似文献
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The paper presents newly obtained data on the mineralogical and geochemical characteristics of Ukrainian endogenic and supergenic diamonds, including pioneering data on the carbon isotopic composition of individual diamond crystals. The endogenic diamonds occur as euhedral microcrystals (their morphology varies from octahedral to rhombododecahedral and cubic) with broadly varying concentrations of the structural nitrogen admixture and with mostly low aggregation of nitrogen centers. According to their carbon isotopic composition, Ukrainian diamonds range from kimberlitic–lamproitic to metamorphic and even carbonado-like, i.e., are polygenetic. Our data confirm the earlier conclusion that the supergenic diamonds are of impact genesis. 相似文献
4.
金刚石由于其独特的物理化学性质,在经济生产与科学研究中均具有重要价值.金刚石形成于地球大于150 km的深度范围内,是人类可以获得的来自地球深部地幔乃至核幔边界的最直接的样品,因此可以为研究地球深部物质组成和物理化学条件提供重要的素材.金刚石由碳元素组成,还含有微量的杂质元素（如氮、硼、氢、氧等）,其中氮和硼元素对于划分金刚石的晶体结构类型发挥着重要的作用.根据金刚石的产出类型,金刚石可以划分为幔源型、超高压变质型、陨石相关型以及蛇绿岩型金刚石.全球约百分之一的幔源型金刚石含有包裹体,对这些包裹体的研究显示,金刚石主要来源于地球150~200 km深度的岩石圈地幔.这些含有包裹体的金刚石中,仅有1%的金刚石来自于地球深部的软流圈、地幔过渡带、下地幔、甚至核幔边界.我国的金刚石产出类型多样,但是,目前仅山东蒙阴、辽宁复县的金伯利岩矿床以及湖南沅水的砂矿具有经济价值.蛇绿岩型金刚石是近年来金刚石研究领域取得的重要进展,该类型金刚石分布在全球多个造山带不同时代、不同构造属性的蛇绿岩地幔橄榄岩和铬铁矿中,被认为是一种新的金刚石的产出类型.相对于其他国家和地区的金刚石的研究,我国的金刚石领域的研究程度相对较低,缺乏对金刚石结构、化学组成以及包裹体组成的系统研究,制约了对我国金刚石成因的认识,限制了我国的金刚石的找矿工作.因此,亟需结合先进的分析手段对我国的金刚石及其围岩做进一步的研究,以期揭示金刚石的形成过程,为金刚石的找矿提供理论基础. 相似文献
5.
对采自我国3个商业性产地山东蒙阴、辽宁瓦房店、湖南常德地区的236片/颗天然钻石样品进行了系统的DiamondViewTM(DV)荧光图像分析,结合CL照相和FTIR的定量计算,探讨了钻石样品DV图像发光结构模式和荧光颜色方面的差异性及其原因。结果表明,3个产地钻石的DV图像和CL图像显示的钻石生长结构基本一致;钻石的发光结构模式与钻石内部氮、氢元素的种类和浓度分布趋势没有明显的一致性,DV图像模式并不完全受钻石类型控制,但DV图像的色调与钻石存在的杂质元素及晶体缺陷有关。钻石的DV图像特征受钻石的生长环境、结晶条件、后期熔蚀、辐照损伤等因素综合制约。从统计学的角度看,3个产地钻石的DV发光模式和荧光颜色有一定的差异,这种差异可以作为区分不同产地来源的钻石的宏观的统计学特征。DiamondViewTM技术在揭示天然钻石生长结构方面和CL发光照相技术效果近似,但更加便利。 相似文献
6.
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.
相似文献7.
V. N. Reutsky A. A. Shiryaev S. V. Titkov M. Wiedenbeck N. N. Zudina 《Geochemistry International》2017,55(11):988-999
The spatial distribution of carbon and nitrogen isotopes and of nitrogen concentrations is studied in detail in three gem quality cubic diamonds of variety II according to Orlov’s classification. Combined with the data on composition of fluid inclusions our results point to the crystallization of the diamonds from a presumably oxidized carbonate fluid. It is shown that in the growth direction δ13C of the diamond becomes systematically lighter by 2–3‰ (from –13.7 to –15.6‰ for one profile and from –11.7 to –14.1‰ for a second profile). Simultaneously, we observe substantial decrease in the nitrogen concentration (from 400–1000 to 10–30 at ppm) and a previously unrecognized enrichment of nitrogen in light isotope, exceeding 30‰. The systematic and substantial changes of the chemical and isotopic composition can be explained using the Burton-Prim-Slichter model, which relates partition coefficients of an impurity with the crystal growth rate. It is shown that changes in effective partition coefficients due to a gradual decrease in crystal growth rate describes fairly well the observed scale of the chemical and isotopic variations if the diamond-fluid partition coefficient for nitrogen is significantly smaller than unity. This model shows that nitrogen isotopic composition in diamond may result from isotopic fractionation during growth and not reflect isotopic composition of the mantle fluid. Furthermore, it is shown that the infra-red absorption at 1332 сm-1 is an integral part of the Y-defect spectrum. In the studied natural diamonds the 1290 сm-1 IR absorption band does not correlate with boron concentration. 相似文献
8.
Previous studies of diamonds from Finsch have shown that eclogitic inclusions are rare at Finsch and that the eclogitic garnet and clinopyroxenes are iron and manganese-rich. In order to expand the current database of information, 93 eclogitic diamonds were selected for this study. Eight diamonds were polished into plates for cathodoluminescence studies and infrared examination of diamond growth and 31 diamonds were cracked to retrieve inclusions. The eclogitic garnets analysed in this study are enriched in Fe and are relatively depleted in Ca and Mg relative to worldwide data. FeO contents for garnet range from 15 to 27 wt.% and MnO contents reach a maximum value of 1.6 wt.%. The eclogitic clinopyroxenes have relatively high FeO contents, up to 14.8 wt.% and K2O contents are low (<0.4 wt.%). Three non-touching garnet–clinopyroxene mineral pairs produce equilibration temperatures of 1138–1179 °C at an assumed pressure of 50 kb. No Type II diamonds were found during this study, all diamonds are of Type IaAB. Total nitrogen contents of Type IaAB diamonds range from 11 to 1520 ppm, with variable aggregation states (up to 84% nitrogen aggregated as B-defects). Distinct infrared characteristics suggest that the Finsch kimberlite sampled either more than one mantle source region of similar age but differing temperature, or two different populations of diamonds with different ages. The diamonds provide evidence of changing mantle conditions during crystallisation. Continuous diamond growth is illustrated by the presence of regular octahedral growth zones, although in some diamonds cubic growth is noted. One diamond shows evidence of platelet degradation, suggesting exposure to high temperatures and/or shearing stresses. 相似文献
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10.
A representative sample of microdiamonds in calc-silicate and garnet-pyroxene-quartz rocks and gneisses from the cross section of an adit driven at the Kumdy-Kol’ deposit (Northern Kazakhstan) has been analyzed. Microdiamonds from these rocks were studied by Fourier-transform infrared spectroscopy for the first time. It has been established that nitrogen impurity content (300–3000 ppm) and nitrogen aggregation degree (14–75%) vary widely and do not correlate with each other. The variation is probably due to the uneven distribution of nitrogen in crystals and to their specific internal structures.The results of the study show that in most diamondiferous rocks, diamonds crystallized from a fluid/melt of composition varying between aqueous-carbonate and aqueous-silicate end-members. Spectroscopy studies partly disagree with literature data on individual nanoinclusions in diamonds. The cause of this discrepancy may be the evolution of the fluid/melt during diamond crystallization. 相似文献
11.
A.S. Stepanov V.S. Shatsky D.A. Zedgenizov N.V. Sobolev 《Russian Geology and Geophysics》2007,48(9):758-769
A unique xenolith of eclogite, 23×17×11 cm in size and 8 kg in weight, was found in the Udachnaya kimberlite pipe. One hundred twenty-four diamond crystals recovered from it were analyzed by a number of methods. The diamonds differ in morphology, internal structure, color, size, and composition of defects and impurities. The xenolith contains diamonds of octahedral and cubooctahedral habits. In cathodoluminescence, the octahedral crystals have a brightly glowing core with octahedral zones of growth and a weakly glowing rim. In the cores of these crystals the N impurity is mostly present in the B1 form (30 to 60%). At the same time, N in the rim is chiefly in the A form. The cubooctahedral crystals show a weak luminescence. The content of nitrogen and degree of its aggregation are close to those in the rim of octahedral crystals. The diversity of morphology and impurity composition of diamonds from the xenolith can be explained by their formation in two stages. At the first stage, the diamonds formed which became the cores of octahedra. After a long-time interruption, at the second stage of diamond formation crystals of cubooctahedral habit appeared and the octahedral crystals were overgrown. Wide variations in nitrogen contents in the xenolith crystals allowed their use to estimate the kinetics of aggregated nitrogen. The data obtained show that the aggregation of A centers into B1 centers in the diamonds is described by a kinetic reaction of an order of 1.5. 相似文献
12.
The diamonds from the Swartruggens dyke swarm are mainly tetrahexahedra, with subsidiary octahedral and cuboid crystals. They are predominantly colourless, with subordinate yellows, browns, and greens. The existence of discrete cores and oscillatory growth structures within the diamonds, together with the recognition of harzburgite, lherzolite, at least two eclogitic and a websteritic diamond paragenesis, variable nitrogen contents, and both Type IaAB and Type Ib–IaA diamonds provides evidence for episodic diamond growth in at least six different environments. The predominance of plastic deformation in the diamonds, the state of nitrogen aggregation, and the suite of inclusion minerals recovered are all consistent with a xenocrystic origin for the diamonds, with the Type Ib–IaA diamonds being much younger than the rest. Mantle storage at a time-averaged temperature of ±1100 °C is inferred for the Type IaAB diamonds. The distribution of mantle xenocrysts of garnet and chromite within the high-grade Main kimberlite dyke compared to the low-grade Changehouse kimberlite dyke strongly suggests that the difference in diamond content is due to an increased eclogitic component of diamonds in the Main kimberlite dyke. 相似文献
13.
最近NGTC实验室检测出多批次CVD合成钻石,这些CVD合成钻石均具有明显的鉴定特征,使用钻石观测仪（DiamondViewTM）观察可见蓝色、橙红色荧光和蓝色磷光以及细密层状生长纹理,光致发光光谱中可见737 nm处的特征发光线.这些特征均与其生长结构及生长过程中进入钻石晶体中的杂质有关.笔者以最近检测过程中发现的一颗CVD合成钻石为例,使用高倍率显微技术对其层状结构的微细特征及其在钻石观测仪下的荧光特征的关系进行了详细观察和对比.结果显示,此样品与之前检测到的CVD合成钻石略有差异.此次检测到的样品在钻石观测仪（DiamondViewTM）下观察具有较宽的层状生长分区,层与层之间的分界线十分明显且在高倍显微镜下也可见到细微的生长特征.通过对样品特征的分析,了解了晶体生长过程中多阶段生长条件的变化,更直观的展现了CVD合成钻石的生长过程. 相似文献
14.
I. N. Bogush Z. V. Spetsius O. E. Koval’chuk B. S. Pomazanskiy 《Geochemistry International》2016,54(8):681-690
FTIR microspectroscopic data were used to construct two-dimension maps showing the distribution of structural impurities and mineral microinclusions in cubic and coated octahedral diamond crystals from the Udachnaya kimberlite pipe in Yakutia. Elevated concentrations of hydrogen and total nitrogen are detected in parts corresponding to the early growth of single-episode growth regions of diamond crystals. These concentrations decrease toward the peripheral portions of these regions. The microinclusions contain water and polyphase mineral associations that preserve a high residual pressure. Microinclusions in the coats of octahedral diamond crystals are dominated by silicates, in which the intensity of IR spectral bands increases toward the peripheries, whereas the cubes posses irregularly distributed domains rich in these phases. The carbonate phases of the microinclusions are distributed according to growth zones of the crystals, and their distribution is often not correlated with the concentrations of structural impurities. The facts that microinclusions in the diamond cuboids are dominated by carbonates and that the rims of the octahedra are dominated by silicates suggest that the diamonds crystallized from dominantly carbonate and silicate fluids/ melts, respectively. The chemical composition of the microinclusions point to an eclogitic paragenesis of the crystals. Facts are obtained that provide support for the earlier hypothesis that cubic diamond crystals and coated octahedral crystals grow at metasomatic interaction between deep fluids and eclogitic rocks in the lithospheric mantle. 相似文献
15.
《International Geology Review》2012,54(8):663-676
Diamond formation from metasomatic fluids, rather than from igneous melts, remains controversial but is paramount to our understanding of diamonds' mantle origin(s). Physical and chemical properties of diamonds, their inclusions, and host eclogites from the Mir kimberlite, Yakutia, Russia form the basis for our evaluation of diamond origin. Mir eclogitic diamonds and their multiple inclusions show a definite break in time and temperature between the formation of the core zones and the rims of the diamonds. Extreme changes in chemistry for multiple diamond inclusions (DIs) between the cores and the rims cannot be accounted for by magmatic fractional crystallization. Evidence also exists for large temperature decreases (40° to 140°C) from the cores to the rims of some diamonds. The distinct changes in nitrogen contents and aggregation states from cores to rims of diamonds would appear to reflect different residence times for these portions of the diamonds in the mantle- i.e., formation of cores and rims at vastly different times (e.g., 2 Gy). Many of the mineral-chemical characteristics, including C and N isotopes and N aggregation states of the diamond, can best be explained by crystallization of the diamonds after formation of the eclogite host. This suggests that the formation of the eclogite and the nucleation and growth of some diamonds are not coeval and possibly not cogenetic. Most diamondiferous eclogite xenoliths probably have never experienced a major magmatic episode (i.e., complete melt stage) after subduction of their crustal protoliths into the mantle. Carbon isotopes in diamond, sulfur isotopes from sulfide DIs, and oxygen isotopes from eclogite minerals all point to crustal protoliths for many eclogites. All of the factors above, taken as a whole, indicate that many eclogitic diamonds are the result of petrogenesis by metasomatism over a prolonged period of time. Introduction of metasomatic fluids facilitates the precipitation of the diamonds, either in tolo or as rims on previously formed diamonds. Inasmuch as some eclogites are considered to be igneous in origine.g., Group-A eclogites of Taylor and Neal (1989)-it is entirely possible that these eclogites may contain truly igneous diamonds. However, even some of these diamonds may have later metasomatic overgrowths. 相似文献
16.
Directional chemical variations in diamonds showing octahedral following cuboid growth 总被引：2，自引：0，他引：2
D. A. Zedgenizov B. Harte V. S. Shatsky A. A. Politov G. M. Rylov N. V. Sobolev 《Contributions to Mineralogy and Petrology》2006,151(1):45-57
A progression from cuboid to octahedral growth has been observed in 16 natural diamonds from Yakutian kimberlites. X-ray and
cathodoluminescence topography have revealed that the change in morphology of diamonds with cloudy cuboid cores may occur
without mixed-habit growth but via generation of numerous octahedral apices on cuboid surfaces and subsequent gradual transformation
into regular octahedral morphology. Nitrogen aggregation in both cuboid and octahedral domains of such diamonds suggests that
they have had a long residence time under mantle conditions. Micro-inclusions in the cuboid domains of the diamonds testify
to the nucleation and growth of cuboid cores from a hydrous-carbonatitic (oxidized) fluid. The transition from cuboid hummocky
growth rich in inclusions to octahedral growth without inclusions may be linked to decreasing supersaturation in the parent
fluid. Measurements of δ13C and Nppm by ion microprobe show that the chemical variations observed between inner cuboid domains and outer octahedral zones commonly
have a systematic character and as such they are probably not due to purely kinetic effects. The peripheral octahedral zones
are always enriched in 13C in comparison with inner cuboid ones, and the total nitrogen content decreases with the change from cuboid to octahedral
growth. The octahedral outer zones show a gradual progressive increase in δ13C, with an overall change of up to 5‰ from the cuboid core (δ13C usually between −8 and −6‰) to the diamond margin (δ13C usually between −4 and −2‰). Decreases in δ13C of this magnitude with a gradual increase in 13C may be attributed to the Rayleigh fractionation operating on a single parent fluid of close to normal mantle δ13C composition with diamond precipitating by the reduction of carbonatitic fluid in a closed system. However, one sample shows
a variation of δ13C of approximately −17 to −6‰ and therefore suggests a possible change of fluid source composition from one containing subducted
crustal organic carbon to one with common mantle carbon.
An erratum to this article can be found at 相似文献
17.
G. K. Khachatryan O. V. Palazhchenko V. K. Garanin P. V. Ivannikov E. M. Verichev 《Moscow University Geology Bulletin》2008,63(2):86-94
The internal structures of 78 diamond crystals from the Karpinsky-1 pipe in the Arkhangelsk Province and the distributions of structural impurities in them were examined by the methods of cathode luminescence and IR spectroscopy. Three generations of diamonds were found in the pipe. Diamonds of the first and second generations presumably originated in an ultramafic and eclogite mantle medium. Diamonds of the third generation, which are very common in the pipe, show a fibrous internal structure and anomalously high concentrations of nitrogen and hydrogen; they originated under disequilibrium conditions. The third-generation diamonds differ by the set of their typomorphic features from diamonds of kimberlite origin and show some similarity with diamonds from metamorphic rocks. We hypothesize that the third-generation diamonds from Katpinsky-1 pipe could originate in a proto-kimberlitic melt. 相似文献
18.
Microinclusions analyzed in a coated diamond from the Diavik mine in Canada comprise peridotitic minerals and fluids. The fluids span a wide compositional range between a carbonatitic melt and brine. The diamond is concentrically zoned. The brine microinclusions reside in an inner growth zone and their endmember composition is K19Na25Ca5Mg8Fe3Ba2Si4Cl32 (mol%). The carbonatitic melt is found in an outer layer and its endmember composition is K11Na21Ca11Mg26Fe7Ba2Si10Al3P2Cl5. The transition in inclusion chemistry is accompanied by a change in the carbon isotopic composition of the diamond from −8.5‰ in the inner zone to −12.1‰ in the outer zone. We suggest that this transition reflects mixing between already evolved brine and a freshly introduced carbonatitic melt of different isotopic composition.
The compositional range found in diamond ON-DVK-294 is the widest ever recorded in a single diamond. It closes the gap between brine found in cloudy octahedral diamonds from South Africa and carbonatitic melt analyzed in cubic diamonds from Zaire and Botswana. Thus, all microinclusions analyzed to date fall along two arrays connecting the carbonatitic melt composition to either a hydrous-silicic endmember or to a brine endmember. This connection suggests that many diamonds are formed from fluids derived form a mantle source not significantly influenced by local heterogeneities. 相似文献
19.
On the possibility of a kinetic fractionation of nitrogen stable isotopes during natural diamond growth 总被引：2，自引：0，他引：2
Pierre Cartigny Jeff W. Harris Randi Davies Marc Javoy 《Geochimica et cosmochimica acta》2003,67(8):1571-1576
In a diamond from New South Wales (Australia), cubic and octahedral growth sectors, as identified by cathodoluminescence (CL), show slight differences in N-contents of 29 and 42 ppm respectively but no significant differences in either δ13C, δ15N and nitrogen aggregation state with values at +1.96‰, +19.4‰, and 25% Type IaAB aggregation, respectively.Two gem cubes from the Orapa kimberlite (Botswana) were studied by CL revealing a nonfaceted cubic growth. Accordingly, nine other gem cubes were combusted and yielded δ13C-values from -5.33‰ to -6.63‰, δ15N from -1.0‰ to -5.5‰, and nitrogen contents from 914 to 1168 ppm, with nitrogen aggregation state being only Type IaA (zero % B). The gem cubes show striking similarities to fibrous/coated diamonds, not only in both δ13C ranges (less than 3‰ from -5 to -8‰), but also in the high levels of nitrogen (≈ 1000 ppm), suggesting that the two diamond types are related. Additionally, no δ15N variation was detected between the cube and octahedral growth sectors of the Australian diamond, in the cube sectors of the nine gem cubes from Botswana, nor in fibrous/coated diamonds previously studied. These analyses contrast with an earlier study on a synthetic diamond, which reported a strong kinetic fractionation of N-isotopes of about 40‰ between cube and octahedral growth. The present evidence, therefore, suggests that kinetic fractionation of N-isotopes does not operate during natural diamond formation. 相似文献
20.
The relationship between the distribution of nitrogen impurity centres in diamond crystals and their internal structure and mechanism of growth 总被引：1，自引：0，他引：1
Fifty diamond crystals of different morphological types (octahedra, dodecahedroids, cubes and single tetrahexahedroid) with differing internal structures were examined using methods of cathodoluminescence (CL), anomalous birefringence and local infrared (IR) analysis. The main objective of the study was to examine the regularities of nitrogen impurity distribution in diamond with differing internal structures. Almost all the analyzed octahedra, as well as dodecahedroids with zonal structures and the blocky dodecahedroids, are characterized either by nearly isothermic growth conditions or by a decrease in formation temperature during the crystallization process. In contrast to zoned octahedra and dodecahedroids, dodecahedroids with zonal–sectorial and sectorial internal structures show a notably different distribution of nitrogen defects, with Ntot generally decreasing from crystal cores to marginal areas, and degree of nitrogen aggregation increasing in the same direction. From this, it would follow that in these crystals, the temperature of diamond formation of the outer crystal zones is approximately 40–50 °C higher than that of the inner zones. The same result (15 to 80 °C) was obtained for diamond crystals with cubic habit, which generally show a fibrous internal structure, reflecting normal mechanisms of growth. The anomalous distribution of nitrogen centres in diamond crystals that grew through the normal mechanism, with a high rate of growth and in an oversaturated medium, might point to non-equilibrium relationships between the concentrations of different nitrogen centres. It is likely that in crystals of this type, the rate of growth is higher than the rate of structural nitrogen aggregation. Thus, it appears that in these peculiar crystals of diamond we deal with non-equilibrium concentrations of nitrogen B centres and, consequently, with anomalous, non-actual diamond formation temperatures. 相似文献