Carbon isotopic composition of diamonds from the Archangelsk diamond province

The first data are reported on the carbon isotopic composition of diamond crystals from the Grib pipe kimberlite deposit of the Archangelsk diamond province (ADP). The δ¹³C value of the crystals ranges from ?2.79 to ?9.61‰. The isotopic composition of carbon was determined in three zoned crystals (δ¹³C of ?5.8 ?6.96 ‰, ?5.64/ ?5.85 ‰, and ?5.94/ ?5.69 ‰), two “diamond in diamond” samples (diamond inclusion with δ¹³C of ?4.05 and ?6.34 ‰ in host diamond crystals with δ¹³C of ?8.05 and ?7.54 ‰, respectively), and two samples of coated diamonds (cores with δ¹³C of ?6.98 and ?6.78‰ and coats with δ¹³C of ?7.51 and ?8.01 ‰, respectively). δ¹³C values were obtained for individual diamond crystals from bort-type aggregates (δ¹³C of ?4.24/ ?4.05 ‰, ?6.58/ ?7.48 ‰, and ?5.48/ ?6.08 ‰). Correlations were examined between the carbon isotopic composition of diamonds and their crystal morphology; the color; the concentration of nitrogen, hydrogen, and platelet defects; and mineral inclusions content. It was supposed that the observed δ¹³C variations in the crystals are most likely related to the fractionation of carbon isotopes rather than to the heterogeneity of carbon sources involved in diamond formation. The isotopic characteristics of diamonds from the Grib pipe were compared with those of previously investigated diamonds from the Lomonosov deposit. It was found that diamonds from these relatively closely spaced kimberlite fields are different; this also indicates the existence of spatially localized peculiarities of isotope fractionation in processes accompanying diamond formation.     

First diamonds from placers in Primorie

The paper reports the results obtained by the detailed studying of carbonado (the first find in a gold placer in Primorie) and a collection of diamonds that was confiscated in 1937 from a poaching small digger and was kept safe at the Nezametnyi mine (near the village of Vostretsovo), which had developed this placer deposit. In the concentrate from the placer, carbonado is associated with green corundum, various ilmenite, zircon titanian amphiboles and pyroxenes, rutile, anatase, and fragments of subvolcanic biotite picrites. All of these minerals, native aluminum, and tin occur as inclusions in the diamonds. The carbonado from Primorie was determined to be practically identical to this mineral from Brazil, has a porous structure, is characterized by orange luminescence, contains inclusions of Y, Ce, La, Ba, and Sr phosphates, and has an isotopically light composition of its carbon (¹³C from ?25 to ?32‰). Pores of the carbonado aggregates contain clusters of diamond crystals. The collection of diamonds from an unknown source included six gem-quality transparent crystals, one rounded ballas, two cuboctahedral crystals (one of greenish and the other of silver-gray color, both with outer coats), and one black carbonado grain. The data obtained on the mineralogy of the diamonds have demonstrated that they are completely identical to this mineral from kimberlites and lamproites but bear traces of intense dissolution, fragmentation, multiple recrystallization, and graphitization at defects, which are the most widespread in the ballas. One of the crystals was determined to contain inclusions: aggregates of potassic omphacite (0.50 wt % K₂O) and corundum. Ilmenite (containing up to 8 wt % MgO), titanaugite, kaersutite (4 wt % TiO₂, 0.8 wt % K₂O), and churchite (aqueous phosphate) were obtained from the core of the ballas. The titanaugite, kaersutite, and ilmenite were proven to be compositionally analogous to these minerals from picrites occurring near the placer. The carbon isotopic composition δ¹³C of the cores of the single diamond crystals varies from ?6 to ?11‰. The margins of the grains were proved to be enriched in the light carbon isotope (δ¹³C from ?19 to ?21‰). The gem-quality transparent diamond crystals are characterized by blue luminescence, and the color of luminescence in the carbonado varies from orange red in the bulk of the aggregate to yellowish green in its core. The aforementioned transformations of diamonds were likely caused by their transportation in pipes of micaceous picrites of the Jurassic meymechite complex. The carbonado are thought to correspond to the final stage of the metastable recrystallization (in pores, within the temperature range of the rutile-anatase transition) of the original isotopically heavy diamonds under the effect of various oxidizers (H₂O, CO₂, F, and others) and in the presence of catalytically acting REE, Ti, and P. The primary diamond source (kimberlite or lamproite) can be older and more distant from the study area. The complete geological analogy between the study area in Primorie, Kalimantan Island in Indonesia, and West Australia (where no sources of the placers are known) led us to consider the territory of Primorie as promising for exploration for diamondiferous placers.     

Causes of variations in morphology and impurities of diamonds from the Udachnaya Pipe eclogite

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.     

Origin of disequilibrium diamond crystals from Karpinsky-1 kimberlite pipe using data from cathode luminescence and infra red spectroscopy

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.     

Aspects of diamond mineralisation and distribution at the Helam Mine, South Africa

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.     

Kankan diamonds (Guinea) III: δ13C and nitrogen characteristics of deep diamonds

Diamonds from the Kankan area in Guinea formed over a large depth profile beginning within the cratonic mantle lithosphere and extending through the asthenosphere and transition zone into the lower mantle. The carbon isotopic composition, the concentration of nitrogen impurities and the nitrogen aggregation level of diamonds representing this entire depth range have been determined. Peridotitic and eclogitic diamonds of lithospheric origin from Kankan have carbon isotopic compositions ('¹³C: peridotitic -5.4 to -2.2‰; eclogitic -19.7 to -0.7‰) and nitrogen characteristics (N: peridotitic 17-648 atomic ppm; eclogitic 0-1,313 atomic ppm; aggregation from IaA to IaB) which are generally typical for diamonds of these two suites worldwide. Geothermobarometry of peridotitic and eclogitic inclusion parageneses (worldwide sources) indicates that both suites formed under very similar conditions within the cratonic lithosphere, which is not consistent with a derivation of diamonds with light carbon isotopic composition from subducted organic matter within subducting oceanic slabs. Diamonds containing majorite garnet inclusions fall to the isotopically heavy side ('¹³C: -3.1‰ to +0.9‰) of the worldwide diamond population. Nitrogen contents are low (0-126 atomic ppm) and one of the two nitrogen-bearing diamonds shows such a low level of nitrogen aggregation (30% B-centre) that it cannot have been exposed to ambient temperatures of the transition zone (̿,400 °C) for more than 0.2 Ma. This suggests rapid upward transport and formation of some Kankan diamonds pene-contemporaneous to Cretaceous kimberlite activity. Similar to these diamonds from the asthenosphere and the transition zone, lower mantle diamonds show a small shift towards isotopic heavy compositions (-6.6 to -0.5‰, mode at -3.5‰). As already observed for other mines, the nitrogen contents of lower mantle diamonds were below detection (using FTIRS). The mutual shift of sublithospheric diamonds towards isotopic heavier compositions suggests a common carbon source, which may have inherited an isotopic heavy composition from a component consisting of subducted carbonates.     

Chromatographic study of formation conditions of rhombododecahedral diamond crystals

The results of chromatographic study of the formation of rhombododecahedral diamonds synthesized in the Fe-Ni-(Ti)-C system at 5.5–6.0 GPa and 1350–1450°C are presented, including crystals with rounded surfaces of the rhombododecahedron with parallel striation, which are morphological analogues of natural diamonds abundant at various kimberlite, lamproite, and placer deposits. Chromatography was performed at 150°C with mechanical breakup of diamonds. The stable release of methane when diamonds of habit {110} are crushed is established. It is concluded that the appearance of the habit rhombododecahedron may be related not only to the effect of temperature and pressure on crystal growth but also to reductive conditions of crystallization. At the same time, the appearance of significant amounts of hydrocarbons in the system probably results in stopping of the growth of faces {110} and {100} and, instead, formation of specific surfaces that are composed of microscopic accessories faced by planes {111}.     

Constraints on diamond genesis from the study of the dependence of diamond properties on the composition of kimberlites and lamproites

It was shown that the crystal morphology, content, and size of diamonds depend on the concentrations of silica, magnesium, calcium, and carbon dioxide in the host kimberlites and lamproites. The character of this dependence suggests that the viscosity of the initial melts of these rocks was the main control of the morphology and properties of diamond crystals and indicates a magmatic genesis for this mineral. Two genetic varieties of diamond crystals were distinguished: larger residual grains coeval with the formation of the sources of kimberlite and lamproite magmas during the slow high-pressure fractionation of the near-bottom peridotite layer of the global magma ocean and smaller early magmatic grains, which crystallized during the decompression-friction transformation of kimberlite and lamproite protoliths into magmas.     

Comparative characteristic of diamonds with olivine inclusions from the Ebelyakh placer and kimberlite pipes of the Yakutian Diamondiferous Province

The results of morphological examination and the character of the structural orientation and estimation of residual pressure calculated from spectra of combination dispersion in olivine inclusions within diamonds of the Ebelyakh placer and kimberlite pipes of the Yakutian Diamondiferous Province are presented. The data analysis aimed at revealing indications of similarity and/or differences between diamonds from the pipes and the placer. Differences in the structural orientation and spectra of combination dispersion of the inclusions of olivine in dodecahedroids of placers of the northeastern part of the Siberian Platform support the assumption of their non-kimberlite nature.     

Peculiarities of Diamonds in Eclogitic Xenoliths from the Komsomolskaya Kimberlite Pipe,Yakutia

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.

     

New insights into the occurrence of C-depleted carbon in the mantle from two closely associated kimberlites: Letlhakane and Orapa, Botswana

Carbon isotope measurements on diamonds from the Letlhakane kimberlite, and the analyses of their inclusions, permit the examination of km-scale mantle-composition variations by comparing the results with those for the nearby Orapa kimberlite. Diamonds from Letlhakane have a wide range in carbon isotopic composition (−3‰ to −21‰); however, the relative abundance of diamonds depleted in ¹³C is significantly lower than in the Orapa kimberlite. Most of the ¹³C-depleted diamonds belong to the eclogictic or websteritic paragenesis. The relative abundance of inclusions in diamonds and their composition indicate that there are significant differences in petrology in the mantle below the two locations. At Letlhakane, peridotitic compositions are more prevalent than at Orapa and the protolith of P-Type inclusions in diamonds may have experienced a higher degree of partial melting at Letlhakane compared to Orapa. P/T estimates for both W- and E-Type diamonds indicate that a region of ¹³C-depletion may exist beneath the two kimberlites. The relationships between carbon isotopic composition of the host diamond and the Al₂O₃/Cr₂O₃ ratios of their websteritic and eclogitic garnet inclusions indicate that the low δ¹³C regions may represent a primary mantle feature, unrelated to a crustal component.     

Carbonates and sources of fluids in ores and metasomatites of the Ermakovka fluorite-bertrandite-phenacite deposit (western Transbaikalia)

We present results of isotope-geochemical study of the Ermakovka F-Be deposit, including data on the oxygen and carbon isotope compositions in dolomite and calcite marbles and in carbonates accompanying skarns, of early and late stages of ore formation and of post-ore parageneses. To elucidate the sources of fluids participated in the ore formation, we calculated the oxygen isotope composition in water and the hydrogen isotope composition in hydroxyl-containing minerals. Phlogopite in marbleized dolomites, vesuvianite and amphibole in skarns, eudidimite and bertrandite in ore parageneses, and bavenite formed during post-ore processes are analyzed. Most of the ore-stage minerals are depleted in heavy oxygen. Their 5¹⁸O values are lower than 5-6%c (SMOW). Oxygen in carbonate minerals of the initial stage (dolomite and bastnaesite) is heavier (1.3-4.9%c) than that in calcite (+ 2 to -3.7%c). The 5¹⁸O values of water in equilibrium both with carbonate and with silicate minerals (-4 to -14%c) suggest the contribution of meteoric water to the mineral formation. A magmatic fluid (5¹⁸O from + 6 to + 9%c) participated in the skarn formation at the initial stage, and a meteoric fluid, at the final stage (5¹⁸O from -1 to -9%c). A meteoric source is confirmed by the depleted hydrogen isotope composition in minerals (5D from -119 to -192%c).     

Diamondiferous Archean rocks of the Olondo greenstone belt (western Aldan–Stanovoy shield)

Diamond from metaultramafic rocks of the Mesoarchean (2.96–3.0 Ga) Olondo greenstone belt, located in the western Aldan–Stanovoy shield, has been studied. Diamonds occur in lenses of olivine–serpentine–talc rocks within metaultramafic rocks of intrusive habit, whose composition corresponds to peridotite komatiites. All diamonds from the metaultramafic rocks are crystal fragments 0.3 to 0.5 mm in size. Morphological examination has revealed laminar octahedra, their transitional forms to dodecahedroids, crystals with polycentric faces, and spinel twins. The crystals vary in photoluminescence color: dark blue, green, yellow, red, or albescent. Characteristic absorption bands in crystals point to nitrogen impurities in the form of A and B1 defects and tabular B2 defects. The crystals studied belong to the IaA/B type, common among natural diamonds. The overall nitrogen content varies from < 100 to 3800 ppm. The relative content of nitrogen in B1 centers varies from 0 to 94%, pointing to long stay in the mantle. The carbon isotope ratio in the diamonds, ¹³C = ? 26‰, is indicative of involvement of subducted crust matter in diamond formation in the Archean.     

Diamond growth from oxidized carbon sources beneath the Northern Slave Craton, Canada: A δC-N study of eclogite-hosted diamonds from the Jericho kimberlite

Diamonds from high- and low-MgO groups of eclogite xenoliths from the Jericho kimberlite, Slave Craton, Canada were analyzed for carbon isotope compositions and nitrogen contents. Diamonds extracted from the two groups show remarkably different nitrogen abundances and δ¹³C values. While diamonds from high-MgO eclogites have low nitrogen contents (5-82 ppm) and extremely low δ¹³C values clustering at ∼−40‰, diamonds from the low-MgO eclogites have high nitrogen contents (>1200 ppm) and δ¹³C values from −3.5‰ to −5.3‰.Coupled cathodoluminescence (CL) imaging and SIMS analysis of the Jericho diamonds provides insight into diamond growth processes. Diamonds from the high-MgO eclogites display little CL structure and generally have constant δ¹³C values and nitrogen contents. Some of these diamonds have secondary rims with increasing δ¹³C values from −40‰ to ∼−34‰, which suggests secondary diamond growth occurred from an oxidized growth medium. The extreme negative δ¹³C values of the high-MgO eclogite diamonds cannot be produced by Rayleigh isotopic fractionation of average mantle-derived carbon (−5‰) or carbon derived from typical organic matter (∼−25‰). However, excursions in δ¹³C values to −60‰ are known in the organic sedimentary record at ca. 2.7 and 2.0 Ga, such that diamonds from the high-MgO eclogites could have formed from similar organic matter brought into the Slave lithospheric mantle by subduction.SIMS analyses of a diamond from a low-MgO eclogite show an outer core with systematic rimwards increases in δ¹³C values coupled with decreases in nitrogen contents, and a rim with pronounced alternating growth zones. The coupled δ¹³C-nitrogen data suggest that the diamond precipitated during fractional crystallization from an oxidized fluid/melt from which nitrogen was progressively depleted during growth. Model calculations of the co-variation of δ¹³C-N yielded a partition coefficient (K_N) value of 5, indicating that nitrogen is strongly compatible in diamond relative to the growth medium. δ¹³C values of diamond cores (−4‰) dictate the growth medium had higher δ¹³C values than primary mantle-derived carbon. Therefore, possible carbon sources for the low-MgO eclogite diamonds include oxidized mantle-derived (e.g. protokimberlite or carbonatite) fluids/melts that underwent some fractionation during migration or, devolatilized subducted carbonates.     

试对贵州贵定平伐泥盆系碎屑岩金刚石信息的思考

本文根据贵定平伐地区水系砂矿金刚石和泥盆系碎屑岩金刚石信息,结合黔东钾镁煌斑岩乃至华北地台金刚石成矿于奥陶纪(末)的时间域,贵州地史演化特征和此时都匀运动的地质构造格架,综合分析认为,仍处海相沉积建造进程中的黔东有一系列(含金刚石)钾镁煌斑岩侵入,作为上扬子地台中相对刚性的黔中隆起块体,应更利于钾镁煌斑岩型甚至金伯利岩型金刚石的成矿,贵定平伐泥盆系碎屑岩金刚石或许就是来源于黔中隆起区原生金刚石矿的剥蚀扩散补给,并因此相伴形成碎屑岩区水系砂矿金刚石及其指示矿物的重砂异常。     

An infrared investigation of inclusion-bearing diamonds from the Venetia kimberlite,Northern Province,South Africa : implications for diamonds from craton-margin settings

The Venetia kimberlites in the Northern Province of South Africa sampled diamonds from the lithosphere underlying the Central Zone of the Limpopo Belt. Given the general correlation of diamond-bearing kimberlites with old stable cratons, this tectonic setting is somewhat anomalous and, therefore, it is desirable to characterise the diamonds in terms of their infrared characteristics. A suite of diamonds of known paragenesis from the Venetia mine spans a large range of nitrogen concentrations from less than the detection limit to 1,355 ppm. Diamond nitrogen contents are, on average, higher in the eclogitic diamond population relative to the websteritic and peridotitic diamonds. Nitrogen aggregation states are variable, ranging from almost pure type IaA diamond (poorly aggregated nitrogen) to pure type IaB diamond (highly aggregated nitrogen). On a nitrogen aggregation diagram two distinct groups can be identified based on nitrogen content and nitrogen aggregation state. These are a minor population of diamonds with nitrogen contents generally higher than 500 ppm and nitrogen aggregation states of less than 40% IaB, and another, dominant population that is characterised by higher and more variable nitrogen aggregation. The unusually aggregated nature of the majority of the diamonds analysed is unique to Venetia relative to other intrusives on the Kaapvaal-Kalahari craton, but is similar to aggregation states observed for diamonds from other craton margin or adjacent mobile belt settings such as the Argyle lamproite and the George Creek kimberlite. This could be a consequence of diamond mantle residence at mantle temperatures higher than the norm for other kimberlites from the interior of cratons. Deformation of the mantle, associated with dynamic processes such as orogenesis or subduction, might also be responsible for accelerating the rate of nitrogen aggregation in these diamonds. Low numbers of diamonds with degradation of platelets at the Venetia kimberlite, relative to diamonds from the Argyle lamproite, indicate that deformation was at a significantly lower level. The comparatively low value of diamonds from Argyle (at approximately US8/carat) as opposed to Venetia (US8/carat) as opposed to Venetia (US90/carat) is in large part because of the very high abundance of brown diamonds at Argyle. Therefore, it is apparent that deformational history of the mantle in which the diamonds were resident prior to or during sampling by the host may have an important role to play in the profitability of a primary diamond deposit. The apparently consistent association of diamonds with unusually aggregated nitrogen with kimberlites, or lamproites intruded into craton margin or mobile belt settings suggests that it may be possible to recognise such contributory sources in alluvial diamond deposits, through the study of the infrared characteristics of the diamonds. Electronic supplementary material to this paper can be obtained by using the Springer Link server located at http://dx.doi.org/10.1007/s00410-002-0385-2     

Metal films on the surfaces and within diamond crystals from Arkhangelskaya and Yakutian diamond provinces

Representative samples of diamonds from five kimberlite pipes (Lomonosovskaya, Archangel’sk, Snegurochka, XXIII Congress of the Communist Party of the Soviet Union (CPSU), and Internationalnaya) of the Arkhangelskaya and Yakutian diamond provinces in Russia have been studied. Thirty-three varieties of metal films have been identified as syngenetic associated minerals. The films consist of 15 chemical elements that occur in the form of native metals and their natural alloys. Remnants of metal films were detected within diamond crystals. The metal films coating diamonds are a worldwide phenomenon. To date, these films have been described from Europe, Asia, South America, and Africa. Native metals, their alloys, and intermetallides are actual companion minerals of diamond.     

Diamonds from the Poiskovaya,Zapolyarnaya, and Leningrad kimberlite pipes,Northern Yakutia: Correlation of carbon isotopic composition and nitrogen content as an indicator of fluid diamond formation

Compared to most studied kimberlite pipes of the Yakutian province, diamonds from the Poiskovaya, Zapolyarnaya, and Leningrad pipes (about 100 determinations) are characterized by a decrease in the average δ¹³C (−4.59, −4.50,−4.04‰) and by relatively low average nitrogen contents (93, 254, 304 ppm, respectively). These pipes also differ in the relative abundance of alpha-1 group crystals in Galimov’s classification. Based on a stable combination of morphology and properties, we distinguished diamond populations of the common origin. All of them have significant a negative correlation between δ¹³C and the nitrogen content. This correlation is considered to be a result of synchronous and progressive loss of nitrogen and the light isotope ¹²C in the medium during the diamond formation. The conclusion is drawn that the alpha-1 crystals were formed in the open fluid system. The pyrolysis of ethane—C₂H₆ → CH₄ + H₂ + C_diam—is assumed to be a model of diamond precipitation from fluid. The pressure release due to extension deformation of the mantle under tectonic action might be a factor shifting this reaction toward diamond formation.     

Mineral inclusions in sublithospheric diamonds from Collier 4 kimberlite pipe, Juina, Brazil: subducted protoliths, carbonated melts and primary kimberlite magmatism

We report on a suite of diamonds from the Cretaceous Collier 4 kimberlite pipe, Juina, Brazil, that are predominantly nitrogen-free type II crystals showing complex internal growth structures. Syngenetic mineral inclusions comprise calcium- and titanium-rich phases with perovskite stoichiometry, Ca-rich majoritic-garnet, clinopyroxene, olivine, TAPP phase, minerals with stoichiometries of CAS and K-hollandite phases, SiO₂, FeO, native iron, low-Ni sulfides, and Ca–Mg-carbonate. We divide the diamonds into three groups on the basis of the carbon isotope compositions (δ¹³C) of diamond core zones. Group 1 diamonds have heavy, mantle-like δ¹³C (−5 to −10‰) with mineral inclusions indicating a transition zone origin from mafic protoliths. Group 2 diamonds have intermediate δ¹³C (−12 to −15‰), with inclusion compositions indicating crystallization from near-primary and differentiated carbonated melts derived from oceanic crust in the deep upper mantle or transition zone. A ²⁰⁶Pb/²³⁸U age of 101 ± 7 Ma on a CaTiSi-perovskite inclusion (Group 2) is close to the kimberlite emplacement time (93.1 ± 1.5 Ma). Group 3 diamonds have extremely light δ¹³C (−25‰), and host inclusions have compositions akin to high-pressure–temperature phases expected to be stable in pelagic sediments subducted to transition zone depths. Collectively, the Collier 4 diamonds and their inclusions indicate multi-stage, polybaric growth histories in dynamically changing chemical environments. The young inclusion age, the ubiquitous chemical and isotopic characteristics indicative of subducted materials, and the regional tectonic history, suggest a model in which generation of sublithospheric diamonds and their inclusions, and the proto-kimberlite magmas, are related genetically, temporally and geographically to the interaction of subducted lithosphere and a Cretaceous plume.     

Diamonds in the Attawapiskat area of the Superior craton (Canada): evidence for a major diamond-forming event younger than 1.1 Ga

Here, we compare nitrogen aggregation characteristics and carbon isotopic compositions in diamonds from Mesoproterozoic (T1) and Jurassic (U2) kimberlites in the Attawapiskat area—the first diamond-producing area on the Superior craton. The T1 kimberlite sampled diamonds from the lithospheric mantle at 1.1 Ga, at the same time as the major Midcontinent Rift event. These diamonds have a narrow range in δ¹³C (mode of ?3.4 ‰), with compositions that overlap other diamond localities on the Superior craton. Some diamond destruction must have occurred during the Mesoproterozoic in response to the thermal impact of the Midcontinent Rift—the associated elevated geotherm caused a narrow diamond window (<30 km) close to the base of the lithosphere, compared to a wide diamond window of ~85 km following thermal relaxation (sampled by Jurassic kimberlites, such as U2). T1 diamonds have highly aggregated nitrogen, possibly due to the thermal effect of the rift. Diamond-favourable conditions were re-established in the lithospheric mantle after the thermal impact of the Midcontinent Rift dissipated. The poorly aggregated nature of nitrogen in U2 diamonds—compared to highly aggregated nitrogen in diamonds from T1—indicates that renewed diamond formation must have occurred only after the thermal impact of the Midcontinent Rift at 1.1 Ga had subsided and that these newly formed diamonds were subsequently sampled by Jurassic kimberlites. The overall δ¹³C distribution for U2 diamonds is distinct to T1 and other Superior diamonds, further suggesting that U2 diamonds are not related to the older pre-rift diamonds.