The timing of kimberlite magmatism in North America: implications for global kimberlite genesis and diamond exploration

Based on a compilation of more than 100 kimberlite age determinations, four broad kimberlite emplacement patterns can be recognized in North America: (1) a northeast Eocambrian/Cambrian Labrador Sea province (Labrador, Québec), (2) an eastern Jurassic province (Ontario, Québec, New York, Pennsylvania), (3) a Cretaceous central corridor (Nunavut, Saskatchewan, central USA), and (4) a western mixed (Cambrian-Eocene) Type 3 kimberlite province (Alberta, Nunavut, Northwest Territories, Colorado/Wyoming). Ten new U–Pb perovskite/mantle zircon and Rb–Sr phlogopite age determinations are reported here for kimberlites from the Slave and Wyoming cratons of western North America. Within the Type 3 Slave craton, at least four kimberlite age domains exist: I-a southwestern Siluro-Ordovician domain (450 Ma), II-a SE Cambrian domain (540 Ma), III-a central Tertiary/Cretaceous domain (48–74 Ma) and IV-a northern mixed domain consisting of Jurassic and Permian kimberlite fields. New U–Pb perovskite results for the 614.5±2.1 Ma Chicken Park and 408.4±2.6 Ma Iron Mountain kimberlites in the State Line field in Colorado and Wyoming confirm the existence of at least two periods of pre-Mesozoic kimberlite magmatism in the Wyoming craton.

A compilation of robust kimberlite emplacement ages from North America, southern Africa and Russia indicates that a high proportion of known kimberlites are Cenozoic/Mesozoic. We conclude that a majority of these kimberlites were generated during enhanced mantle plume activity associated with the rifting and eventual breakup of the supercontinent Gondwanaland. Within this prolific period of kimberlite activity, there is a good correlation between North America and Yakutia for three distinct short-duration (10 my) periods of kimberlite magmatism at 48–60, 95–105 and 150–160 Ma. In contrast, Cenozoic/Mesozoic kimberlite magmatism in southern Africa is dominated by a continuum of activity between 70–95 and 105–120 Ma with additional less-prolific periods of magmatism in the Eocene (50–53 Ma), Jurassic (150–190) and Triassic (235 Ma). Several discrete episodes of pre-Mesozoic kimberlite magmatism variably occur in North America, southern Africa and Yakutia at 590–615, 520–540, 435–450, 400–410 and 345–360 Ma. One of the surprises in the timing of kimberlite magmatism worldwide is the common absence of activity between about 250 and 360 Ma; this period is even longer in southern Africa. This >110 my period of quiescence in kimberlite magmatism is likely linked to relative crustal and mantle stability during the lifetime of the supercontinent Gondwanaland.

Economic diamond deposits in kimberlite occur throughout the Phanerozoic from the Cambrian (Venetia, South Africa; Snap Lake and Kennady Lake, Canada) to the Tertiary (Mwadui, Tanzania; Ekati and Diavik in Lac de Gras, Canada). There are clearly some discrete periods when economic kimberlite-hosted diamond deposits formed globally. In contrast, the Devonian event, which is such an important source of diamonds in Yakutia, is notably absent in the kimberlite record from both southern Africa and North America.     

Oxidation states of the upper mantle recorded by megacryst ilmenite in kimberlite and type A and B spinel lherzolites

The intrinsic oxygen fugacities of homogeneous, inclusion-free, megacryst ilmenites from the Frank Smith, Excelsior, Sekameng and Mukorob kimberlite pipes in southern Africa, and the alnöitic breccia in the Solomon Islands have been determined. Similar measurements have been made of the type A and B spinel peridotites from San Carlos in Arizona. The type A peridotites are characterised by oxygen fugacities close to the iron-wüstite buffer, similar to those of equivalent peridotite specimens from other continental and island arc environments. In strong contrast, the type B peridotites and all of the ilmenite megacrysts range between the oxygen fugacities defined by the nickelnickel oxide and fayalite-magnetite-quartz buffers. A close relationship between type B peridotites, oxidized metasomatizing fluids in the upper mantle and oxidized, silicaundersaturated magma types is suggested. It is unlikely that a solid elemental carbon phase can be an equilibrium crystallization product of kimberlite magmas if the ilmenite megacrysts represent the redox state of kimberlite melts. The ultimate source of the oxidizing fluids and the development of such a wide dispersion (>4 orders of magnitude) in oxygen fugacities of the upper mantle is not clear, but may involve recycled lithosphere, fluids from the lower mantle or result from the relatively rapid diffusion of H₂, compared with other potential volatile species, in the mantle.     

Crystallization of Cr-poor and Cr-rich megacryst suites from the host kimberlite magma: implications for mantle structure and the generation of kimberlite magmas

Cr-poor and Cr-rich megacryst suites, both comprising of varying proportions of megacrysts of orthopyroxene, clinopyroxene, garnet, olivine, ilmenite and a number of subordinate phases, coexist in many kimberlites, with wide geographic distribution. In rare instances, the two suites occur together on the scale of individual megacryst hand specimens. Deformation textures are common to both suites, suggesting an origin related to the formation of the sheared peridotites that also occur in kimberlites. Textures and compositions of the latter are interpreted to reflect deformation and metasomatism within the thermal aureole surrounding the kimberlite magma in the mantle. The megacrysts crystallized in this thermal aureole in pegmatitic veins representing small volumes of liquids derived from the host kimberlite magma, which were injected into a surrounding fracture network prior to kimberlite eruption. Close similarities between compositions of Cr-rich megacryst phases and those in granular lherzolites are consistent with early crystallization from a primitive kimberlite liquid. The low-Cr megacryst suite subsequently crystallized from residual Cr-depleted liquids. However, the Cr-poor suite also reflects the imprint of contamination by liquids formed by melting of inhomogeneously distributed mantle phases with low melting temperatures, such as calcite and phlogopite, present within the thermal aureole surrounding the kimberlite magma reservoir. Such carbonate-rich melts migrated into, and mixed with some, but not all, of the kimberlite liquids injected into the mantle fracture network. Contamination by the carbonate-rich melts changed the Ca–Mg and Mg–Fe crystal–liquid distribution coefficient, resulting in the crystallization of relatively Fe-rich and Ca-poor phases. The implied higher crystal-melt Mg–Fe distribution coefficient for carbonate-rich magmas accounts for the generation of small volumes of Mg-rich liquids that are highly enriched in incompatible elements (i.e. primary kimberlite magmas). The inferred metasomatic origin for the sheared peridotites implies that this suite provides little or no information regarding vertical changes in the thermal, chemical and mechanical characteristics of the mantle.     

The MARID (mica-amphibole-rutile-ilmenite-diopside) suite of xenoliths in kimberlite

Within the ‘glimmerite’ nodules occurring within kimberlite pipes we recognize the MARID suite consisting of varying proportions of mica, amphibole, rutile, ilmenite and diopside. Banding of some specimens is interpreted as cumulate layering. All specimens were deformed either before incorporation into the host kimberlite or during intrusion. Compared with minerals in peridotite xenoliths, the MARID ones are lower in Al₂O₃ and Cr₂O₃, but richer in total iron. The MARID micas, amphiboles, diopsides, ilmenites and probably rutiles contain substantial Fe₂O₃ indicative of oxidizing conditions. The amphibole is potassic richterite. Micas of the megacryst suite in kimberlite have less total iron and Fe₂O₃ than micas of the MARID suite. We suggest that the rocks of the MARID suite crystallized under oxidizing conditions from a magma, chemically similar to kimberlite, within the higher parts of the upper mantle: the presence of amphibole restricts the depth to less than ~ 100 km. A xenolith containing olivine and orthopyroxene as well as minerals similar to but not the same compositionally as MARID-types is interpreted as a metasomite, possibly representing wall-rock of a magma body from which MARID-suite rocks crystallized.     

Melt inclusions from the deep Slave lithosphere: implications for the origin and evolution of mantle-derived carbonatite and kimberlite

Melt inclusions in clinopyroxenes from lherzolitic xenoliths from the deep lithospheric mantle beneath the Slave Craton (Lac de Gras area, Canada) reveal multiple origins for carbonatitic melts. One type of inclusions consists of a series of silicate–carbonate–silicate concentric layers, interpreted to have unmixed under disequilibrium conditions during rapid ascent to the surface. Bulk major- and trace-element compositions are typical of Group 1 kimberlites and quantitative nuclear microprobe imaging of the globules reveals fractionation of related elements (e.g. F–Br, Nb–Ta) between the silicate and carbonate components. The globules probably formed by partial melting of carbonated peridotite, consistent with results of melting experiments and some models for the generation of kimberlite magmas. They provide evidence for a genetic relationship between some carbonate-rich magmas and ultramafic silicate magmas, and for the possibility of unmixing processes of these melts during their evolution.

The second inclusion type comprises carbonate-rich globules interpreted as samples of Mg-carbonatite melt that quenched on ascent to the surface. Bulk major- and trace-element compositions indicate that the melts were derived from a carbonate-rich source and oxygen, carbon, and strontium isotope data are consistent with the involvement of recycled crustal material and suggest that some mantle-derived carbonatites are unrelated to kimberlites.     

Relationships between textural and photoluminescence spectral features of carbonado (natural polycrystalline diamond) and implications for its origin

Field Emission SEM (FESEM) textural observations, crystal size distribution (CSD) analyses, UV-excited luminescence imaging, and photoluminescence (PL) microspectroscopy excited by 488 nm laser were conducted on two texturally contrasting samples of carbonado, a kind of natural polycrystalline diamond from the Central African Republic (CAR). The investigated carbonado samples A and B show extremely different textures: sample A is made up of faceted crystals accompanied by abundant, small rectangular pores, whereas sample B has a granular texture with coarser crystals and scarce, large pores. Diamond crystals smaller than 2–3 µm are enriched in sample A but depleted in sample B. These textural features indicate that sample B diamonds were annealed under thermodynamically stable P–T conditions. The pore characteristics indicate that fluid permeability was higher for sample A than sample B. Photoluminescence (PL) spectra indicate that samples A and B correspond to Group A and B carbonados in the classification of Kagi et al. (1994), respectively, so that sample A reveals emissions from the H3 center without any N–V⁰ derived emission at 575 nm, whereas sample B shows emissions from the 3H center and the N–V⁰ defect. In addition, UV-excited luminescence images and photoluminescence spectra for sample B indicate that the rims of diamond crystals within several microns of a pore show luminescence features similar to those of Group AB carbonados (Kagi et al., 1994), indicating that this Group AB material was formed from Group B by irradiation from pore-filling, radioactive-element-bearing materials at a low temperature. The extent of the low-temperature irradiation is considered to depend on fluid permeability, and the Group A material was strongly irradiated due to its permeable texture whereas the Group B material was not significantly irradiated due to its less permeable granular texture. These results indicate that Group B carbonados have retained their original PL spectral features produced under high pressures and temperatures at mantle depths.     

Change in the viscosity of kimberlite and basaltic magmas during their origin and evolution (prediction)

Based on the analysis of experimental data on the viscosity of mafic to ultramafic magmatic melts with the use of our structure-chemical model for the calculation and prediction of the viscosity of magmas, we have first predicted that diamond-carryihg kimberlite magma must ascend from mantle to crust with considerable acceleration. The viscosity of kimberlite magma decreases by more than three times during its genesis, evolution, and ascent from mantle to crust despite the significant decrease in the temperature of the ascending kimberlite magma (~ 150 °C) and its partial crystallization and degassing. In the case of partial melting (< 1 wt.%) of carbonated peridotite in the mantle at depths of 250-350 km, high-viscosity (~ 35 Pas) kimberlite melts can be generated at ~ 8.5 GPa and ~ 1350 °C, the water content in the melt being up to ~ 8 wt.%, C(OH^-) = 0-2 wt.%, and C(H₂O) = 0-6 wt.%. On the other hand, during the formation of kimberlite pipes, dikes, and sills, the viscosity of near-surface kimberlite melts is much lower (~ 10 Pa s) at ~ 50 MPa and 1200 °C, the volume contents of crystals (V_cr) and the fluid phase (bubbles) (Vfl) are 35 and 5 vol.%, respectively, and the water content in magma, C(OH^-), is 0.5 wt.%. On the contrary, the viscosity of basaltic magmas increases by more than two orders of magnitude during their ascent from mantle to crust. The basaltic magmas which can be generated in the asthenosphere at depths of ~ 100 km have the minimum viscosity (up to ~ 2.3 Pas) at ~ 4.0 GPa, 1350 °C, C(OH^-) - 3 wt.%, and C(H₂O) - 5 wt.%. However, at the final stage of evolution (e.g., during volcanic eruptions), the viscosity of basaltic magma is considerably higher (600 Pa s) at ~ 10 MPa, 1180 °C, V_cr - 30 vol.%, Vf - 15 vol.%, and C(OH^-) - 0.5 wt.%.     

纳米比亚金刚石矿床地质特征、矿床成因及找矿模型

纳米比亚金刚石资源丰富且品质优良,矿床类型以次生砂矿为主。文章对前人的大量研究成果进行分析总结,概述了纳米比亚金刚石矿床的区域地质背景,分析了金刚石矿床的地质特征及矿床成因。对纳米比亚金刚石包裹体氩-氩法定年分析发现,80%的包裹体熔蚀年龄<300Ma,表明大部分纳米比亚碎屑金刚石源自Dwyka期(<300Ma)以后的金伯利岩;纳米比亚金刚石以橄榄岩型(占比46%)和榴辉岩型(占比41%)为主,其余为二辉岩型或介于橄榄岩型-二辉岩型之间;纳米比亚橄榄岩型金刚石包裹体中石榴石-橄榄石平衡矿物的温度为961~1223℃,平均(1107±98)℃;石榴石-斜方辉石的平衡压力多为4.5~6.0GPa。纳米比亚金刚石的找矿有利地区主要为奥兰治河沿线及Oranjemund、卢得立次海岸地区,以次生金刚石砂矿为主。     

Diffusion gradients in an eclogite xenolith from the Roberts Victor kimberlite pipe: (2) kinetics and implications for petrogenesis

In a bimineralic eclogite xenolith (sample JJG41) from the Roberts Victor kimberlite, compositional gradients in clinopyroxene are related to garnet exsolution. Two principal reactions involving clinopyroxene and garnet occur: (i) The net-transfer Al₂Si^-1Mg^-1 which is responsible for garnet growth according to the equation 2Di+Al₂Si^-1Mg^-1=Grossular+MgCa^-1 (reaction 1). This has created substantial compositional gradients in Al, Si and Mg within clinopyroxene. (ii) The exchange of Fe–Mg between garnet and clinopyroxene (reaction 2). During the stage of garnet growth (reaction 1) the lamellae crystallized sequentially as a result of a temperature decrease from around 1400 to 1200° C. This exsolution growth-stage was under the control of Al diffusion in clinopyroxene and at around 1200° C further growth of garnet lamellae became impeded by the sluggishness of Al diffusion in the clinopyroxene host. However, reaction 2 continued during further cooling down to about 1000° C; this temperature being inferred from the constant Fe–Mg partitioning at clinopyroxene-garnet interfaces for the whole set of lamellae. The initial clinopyroxene in JJG41 was probably formed by crystallization from a melt in Archaean time. The cessation of Fe–Mg exchange between garnet and clinopyroxene at about 1000° C may well predate the eruption of the eclogite in kimberlite at around 100 Ma. Kinetic models of reaction are examined for both reactions. Modelling of reaction 1, involving both diffusion and interface migration, allows several means of estimating the diffusion coefficient of Al in clinopyroxene; the estimates are in the range 10^-16-10^-20 cm²/s at 1200° C. These estimates bracket the experimentally determined data for Al diffusion in clinopyroxene, and from these experimental data a preferred cooling rate of about 300° C/Ma is obtained for the period of growth of garnet exsolution lamellae. A geospeedometry approach (Lasaga 1983) suitable for a pure-exchange process (reaction 2) is used to estimate the cooling rate in the later stages of the thermal history (after garnet growth); values 4–40° C/Ma are consistent with the shape of the Fe-diffusion gradients in the clinopyroxene. The extensive thermal history recorded by JJG41, including probable melt involvement at ca. 1400° C, demonstrates the complex evolution of rocks within the mantle. Whilst the notion of formation of mantle eclogites from subducted oceanic crust has become fashionable, it is clear that tracing eclogite geochemical and P-T characteristics backwards from their nature at the time of xenolith eruption, through high-temperature mantle events to the characteristics of the original subducted oceanic crust, will be very complex.     

A Late Cretaceous (ca. 90 Ma) kimberlite event in southern India: Implication for sub-continental lithospheric mantle evolution and diamond exploration

We report groundmass perovskite U–Pb (SIMS) ages, perovskite Nd isotopic (LA-ICPMS) composition and bulk-rock geochemical data of the Timmasamudram diamondiferous kimberlite cluster, Wajrakarur kimberlite field, in the Eastern Dharwar craton of southern India. The kimberlite pipes gave similar Mesoproterozoic ages of 1086 ± 19 Ma (TK-1, microcrystic variant) and 1119 ± 12 Ma (TK-3). However, a perovskite population sampled from the macrocrystic variant of TK-1 gave a much younger Late Cretaceous age of ca. 90 Ma. This macrocrystic kimberlite phase intrudes the Mesoproterozoic microcrystic phase and has a distinct bulk-rock geochemistry. The Nd-isotope composition of the ~ 1100 Ma perovskites in the cluster show depleted ε_Nd(T) values of 2.1 ± 0.6 to 6.7 ± 0.3 whereas the ~ 90 Ma perovskites have enriched ε_Nd(T) values of − 6.3 ± 1.3. The depleted-mantle (DM) model age of the Cretaceous perovskites is 1.2 Ga, whereas the DM model age of the Proterozoic perovskites is 1.2 to 1.5 Ga. Bulk-rock incompatible trace element ratios (La/Sm, Gd/Lu, La/Nb and Th/Nb) of all Timmasamudram kimberlites show strong affinity with those from the Cretaceous Group II kimberlites from the Bastar craton (India) and Kaapvaal craton (southern Africa). As the Late Cretaceous age of the younger perovskites from the TK-1 kimberlite is indistinguishable from that of the Marion hotspot-linked extrusive and intrusive igneous rocks from Madagascar and India, we infer that all may be part of a single Madagascar Large Igneous Province. Our finding constitutes the first report of Cretaceous kimberlite activity from southern India and has significant implications for its sub-continental lithospheric mantle evolution and diamond exploration programs.     

Calculation of the equilibrium C-O-H fluid for ilmenite xenocrysts and estimation of the diamond potential

The composition of the C-O-H fluid is estimated on the basis of the composition of ilmenite xenocrysts. The P-T parameters and oxygen fugacity were assessed for peridotitic ilmenites from the diamond and diamond-free kimberlites of Africa and Yakutia. The composition of the equilibrium C-O-H fluid for these conditions was calculated. The diamond and diamond-free pipes of Angola and Yakutia are characterized by the H₂O-rich and CO₂-rich fluids, respectively. The results indicate that estimation of the composition of the C-O-H fluid in equilibrium with picroilmenite fits the necessary petrological criteria and may be applied for assessment of the diamond potential of mantle objects.     

Syngenetic inclusions of yimengite in diamond from Sese kimberlite (Zimbabwe) — evidence for metasomatic conditions of growth

Syngenetic inclusions of yimengite K (Cr, Ti, Mg, Fe, Al)₁₂O₁₉, a potassium member of the magnetoplumbite mineral group, have been recorded in an octahedral macrodiamond from the Sese kimberlite (50 km south of Masvingo, Zimbabwe). One yimengite inclusion carries lamellae of chromite suggesting peridotitic diamond paragenesis. The diamond and inclusions were studied in situ in a plate polished parallel to (011). Cathodoluminescence (CL) imaging has shown blue colour and octahedral zonation of the diamond, lack of cracks and the location of five yimengites in different growth zones. Nitrogen (N) contents (at. ppm) in the diamond determined by Fourier transform infrared spectroscopy (FTIR) steadily decrease from 576 (core) to 146 (rim). N aggregation (%1aB) is correspondingly 40% in the core and 30% in the rim. Hydrogen (H) content is high in the core, moderate in the intermediate and very high in the rim zones. Four yimengites were dated using the laser ⁴⁰Ar/³⁹Ar method. Three inclusions yielded total gas ages that agree with, or are younger than, or within error of, the Sese kimberlite eruption age (538±11 Ma) but may be compromised by gas loss. One inclusion, with the highest tapped interface gas yield, gave a total gas age of 892±21 Ma that is a likely minimum yimengite age. Time–T °C constraints from N aggregation systematics give a range of possible ages from kimberlite eruption date back to Archean and do not resolve the variable results of the ⁴⁰Ar/³⁹Ar dating. Compared with the published chemistry of yimengite from kimberlites, inclusions from the Sese diamond contain higher Al, Mg, and Sr and have lower concentration of Fe³⁺. The chondrite-normalised REE pattern of the yimengite shows enrichment in LREE and depletion in HREE, but LREE/HREE fractionations are lower than for lindsleyite–mathiasite series mantle titanates and rather similar to the REE concentrations in kimberlite and lamproite rocks. It is suggested that Sese yimengite formed in the lithospheric mantle from metasomatism of chrome spinel by a fluid rich in Ti, K, Ba and LREE.     

Lamproite and kimberlite of the Sayany area: Composition,sources, and diamond potential

Doklady Earth Sciences -     

Phlogopite in mantle xenoliths and kimberlite from the Grib pipe,Arkhangelsk province,Russia:Evidence for multi-stage mantle metasomatism and origin of phlogopite in kimberlite

We present petrography and mineral chemistry for both phlogopite,from mantle-derived xenoliths(garnet peridotite,eclogite and clinopyroxene-phlogopite rocks)and for megacryst,macrocryst and groundmass flakes from the Grib kimberlite in the Arkhangelsk diamond province of Russia to provide new insights into multi-stage metasomatism in the subcratonic lithospheric mantle(SCLM)and the origin of phlogopite in kimberlite.Based on the analysed xenoliths,phlogopite is characterized by several generations.The first generation(Phil)occurs as coarse,discrete grains within garnet peridotite and eclogite xenoliths and as a rock-forming mineral within clinopyroxene-phlogopite xenoliths.The second phlogopite generation(Phl2)occurs as rims and outer zones that surround the Phil grains and as fine flakes within kimberlite-related veinlets filled with carbonate,serpentine,chlorite and spinel.In garnet peridotite xenoliths,phlogopite occurs as overgrowths surrounding garnet porphyroblasts,within which phlogopite is associated with Cr-spinel and minor carbonate.In eclogite xenoliths,phlogopite occasionally associates with carbonate bearing veinlet networks.Phlogopite,from the kimberlite,occurs as megacrysts,macrocrysts,microcrysts and fine flakes in the groundmass and matrix of kimberlitic pyroclasts.Most phlogopite grains within the kimberlite are characterised by signs of deformation and form partly fragmented grains,which indicates that they are the disintegrated fragments of previously larger grains.Phil,within the garnet peridotite and clinopyroxene-phlogopite xenoliths,is characterised by low Ti and Cr contents(TiO_21 wt.%,Cr_2 O_31 wt.% and Mg# = 100 × Mg/(Mg+ Fe)92)typical of primary peridotite phlogopite in mantle peridotite xenoliths from global kimberlite occurrences.They formed during SCLM metasomatism that led to a transformation from garnet peridotite to clinopyroxene-phlogopite rocks and the crystallisation of phlogopite and high-Cr clinopyroxene megacrysts before the generation of host-kimberlite magmas.One of the possible processes to generate low-Ti-Cr phlogopite is via the replacement of garnet during its interaction with a metasomatic agent enriched in K and H_2O.Rb-Sr isotopic data indicates that the metasomatic agent had a contribution of more radiogenic source than the host-kimberlite magma.Compared with peridotite xenoliths,eclogite xenoliths feature low-Ti phlogopites that are depleted in Cr_2O_3 despite a wider range of TiO_2 concentrations.The presence of phlogopite in eclogite xenoliths indicates that metasomatic processes affected peridotite as well as eclogite within the SCLM beneath the Grib kimberlite.Phl2 has high Ti and Cr concentrations(TiO_22 wt.%,Cr_2O_31 wt.% and Mg# = 100× Mg/(Mg + Fe)92)and compositionally overlaps with phlogopite from polymict brecc:ia xenoliths that occur in global kimberlite formations.These phlogopites are the product of kimberlitic magma and mantle rock interaction at mantle depths where Phl2 overgrew Phil grains or crystallized directly from stalled batches of kimberlitic magmas.Megacrysts,most macrocrysts and microcrysts are disintegrated phlogopite fragments from metasomatised peridotite and eclogite xenoliths.Fine phlogopite flakes within kimberlite groundmass represent mixing of high-Ti-Cr phlogopite antecrysts and high-Ti and low-Cr kimberlitic phlogopite with high Al and Ba contents that may have formed individual grains or overgrown antecrysts.Based on the results of this study,we propose a schematic model of SCLM metasomatism involving phlogopite crystallization,megacryst formation,and genesis of kimberlite magmas as recorded by the Grib pipe.     

Mid-ocean ridge and supra-subduction affinities in the Pindos ophiolites (Greece): implications for magma genesis in a forearc setting

The Pindos ophiolitic massif is considered an important key area within the Albanide–Hellenide ophiolitic belt and is represented by two tectonically distinct ophiolitic units: (1) a lower unit, including an intrusive and a volcanic section; and (2) an Upper Ophiolitic Unit, mainly including mantle harzburgites. Both units share similar metamorphic soles and tectono-sedimentary mélanges at their bases.

The intrusive section of the lower unit is composed by an alternation of troctolites with various ultramafic rock-types, including dunites, lherzolites, olivine-websterites, olivine-gabbros, anorthositic gabbros, gabbros and rare gabbronorites.

The volcanic and subvolcanic sequence of the lower unit can geochemically be subdivided into three groups of rocks: (1) basalts and basaltic andesites of the lower pillow section showing a clear high-Ti affinity; (2) basaltic andesites of the upper pillow section with high-Ti affinity, but showing many geochemical differences with respect to the first group; (3) very low-Ti (boninitic) basaltic and basaltic andesitic lava flows separating the lower and upper pillow sections, and dykes widespread throughout the Pindos ophiolites.

These different magmatic groups originated from fractional crystallization from different primary magmas, which were generated, in turn, from partial melting of mantle sources progressively depleted by previous melt extractions. Group 1 volcanics may have derived from partial melting (ca. 20%) of an undepleted lherzolitic source, while group 2 basaltic rocks may have derived from partial melting (ca. 10%) of a mantle that had previously experienced mid-ocean ridge basalt (MORB) extraction. Finally, the Group 3 boninites may have derived from partial melting (ca. 12–17%) of a mantle peridotite previously depleted by primary melt extraction of Groups 1 and 2 primary melts.

In order to explain the coexistence of these geochemically different magma groups, two petrogenetic models formerly proposed for the Albanian ophiolites are discussed.     

Major and trace element variation in ilmenite in the Skaergaard Intrusion: petrologic implications

Ilmenite separates from the floor (LS), roof (UBS), and wall (MBS) sequences of the Skaergaard Intrusion were analyzed for major and trace elements using DCP-AES and ICP-MS techniques. In all three sequences, FeO progressively increases, and MgO and Al₂O₃ progressively decrease with differentiation. Although trace element abundances are, in general, higher in UBS ilmenite than in MBS and LS ilmenite, all three sequences have similar trends for trace element abundance vs. crystallization. Ba, Cs, Rb, Sr, Th, U, Y, and the REEs are excluded elements in ilmenite, and remained at low abundances during differentiation. Cr, Ni, Sc, and V are included elements in ilmenite and other mafic phases, and decreased during differentiation. V contents in ilmenite, however, do not decrease significantly until the upper part of the middle zone, suggesting that magnetite did not begin to affect the magma differentiation trend until much later than when it first appears in the intrusion. Hf, Nb, Ta, and Zr, which are strongly excluded elements in silicates, are included elements in ilmenite. The element ratios Zr/Hf, Y/Ho, Nb/Ta, and U/Th are relatively constant in Skaergaard ilmenite from different parts of the intrusion, suggesting that fluid transport did not significantly effect these elements during differentiation or post-solidification cooling. Calculated partition coefficients for ilmenite in the Skaergaard Intrusion are similar to those reported from previous studies of lunar and terrestrial basalts and kimberlites, and for most elements are significantly lower than those reported for ilmenite in rhyolitic magma. Similar D_i's for Zr, Hf, Nb, and Ta suggest that ilmenite crystallization did not significantly affect Zr/Nb or Hf/Ta in the Skaergaard magma, but the ratios of Zr, Hf, Nb, or Ta to other high field strength elements, such as Th, U, Y, or the REEs, may have been altered by ilmenite fractionation.     

Eocene magmatism(Maden Complex) in the Southeast Anatolian Orogenic Belt: Magma genesis and tectonic implications

The origin and geodynamic setting of the Maden Complex, which is situated in the Bitlis-Zagros Suture Zone in the Southeast Anatolian Orogenic Belt, is still controversial due to lack of systematic geological and geochemical data. Here we present new whole rock major-trace-rare earth element and Sre Nd isotope data from the Middle Eocene volcanic rocks exposed in Maden Complex and discuss their origin in the light of new and old data. The volcanic lithologies are represented mainly by basalt and andesite, and minor dacite that vary from low-K tholeiitic, calc-alkaline, high-K calc-alkaline, and shoshonitic in composition. They exhibit enrichments in large ion lithophile and light rare earth elements, with depletions in high field strength elements. Basaltic rocks have uniform Sr and Nd isotope ratios with high εNd(t) values varying from t5.5 to t6.7, in contrast to, andesitic rocks are characterized by low εNd(t) values ranging from à1.6 to à10. These geochemical and isotopic characteristics indicate that two end-members, a subduction-related mantle source and a continental crust, were involved in the magma genesis. Considering all geological and geochemical data, we suggest that the Eocene Maden magmatism occurred as a post-collisional product by asthenospheric upwelling owing to convective removal of the lithosphere during an extensional collapse of the Southeast Anatolian ranges.