Mineralogy and geochemistry of Devonian ultramafic minor intrusions of the southern Kola Peninsula, Russia: implications for the petrogenesis of kimberlites and melilitites

Minor magmatic intrusions of kimberlite, melilitite and cpx-melilitite occur in the southern part of the Kola Peninsula, Russia, on the Terskii Coast and near the town of Kandalaksha. They yield K-Ar ages of 382 ± 14 Ma and 365 ± 16 Ma, similar to the magmatic rocks from the Kola Alkaline Province. The Terskii Coast kimberlites have mineralogical and geochemical affinities with group 1 kimberlites, whereas the Kandalaksha monticellite kimberlite more closely resembles calcite kimberlites. The lower Al₂O₃ content in the Kola kimberlites indicates a strongly depleted harzburgitic source, while higher Al₂O₃ in the melilitites suggests a lherzolitic source. The Terskii Coast kimberlites are anomalously potassic and significantly enriched in P and Ba compared to other group 1 kimberlites. In contrast, the melilitites are sodic and are anomalously depleted in P compared to worldwide melilitites. Trace element patterns of the Kola kimberlites and melilitites indicate the presence of K- and P-rich phases in the mantle source. To account for the K-troughs shown by both magma types, a K-rich phase such as phlogopite is thought to be residual in their sources; however, the anomalous K-enrichment in the Terskii Coast kimberlites may indicate that an additional metasomatic K-rich phase (e.g. K-richterite and/or a complex K-Ba-phosphate) existed in the kimberlite source. The P-depletion in the melilitites may suggest that a phosphate phase such as apatite remained residual in the melilititic source. However, anomalous P-enrichment in the kimberlites cannot be explained by complete melting of the same phase because the kimberlites are a smaller degree melt; thus, it is most likely that another metasomatic phosphate mineral existed in the source of the kimberlites. The Kola kimberlites and melilitites are all strongly LREE-enriched but the kimberlites have a steeper REE pattern and are significantly more depleted in HREE, indicating a higher proportion of garnet in their source. Higher Nb/Y ratios and lower SiO₂ values in the kimberlites indicate that they were a smaller degree partial melt than the melilitites. The presence of diamonds in the Terskii Coast kimberlites indicates a relatively deep origin, while the melilitites originated from shallower depth. The non-diamondiferous Kandalaksha monticellite kimberlite has lower abundances of all incompatible trace elements, suggesting a higher degree of partial melting and/or a less enriched and shallower source than the Terskii Coast kimberlites. The ⁸⁷Sr/⁸⁶Sr_i, ¹⁴³Nd/¹⁴⁴Nd_i and Pb isotope compositions confirm that the Terskii Coast kimberlites have close affinities with group 1 kimberlites and were derived from an asthenospheric mantle source, while the Kandalaksha monticellite kimberlite and Terskii Coast melilitites were derived from lithospheric mantle. Impact of a Devonian asthenospheric mantle plume on the base of the Archaean-Proterozoic lithosphere of the Kola Peninsula caused widespread emplacement of kimberlites, melilitites, ultramafic lamprophyres and other more fractionated alkaline magmas. The nature of the mantle affected by metasomatism associated with the plume and, in particular, the depth of melting and the stability of the metasomatic phases, gave rise to the observed differences between kimberlites and the related melilitites and other magmas. Received: 3 March 1997 / Accepted: 7 October 1997     

Sr and Nd isotope data of apatite,calcite and dolomite as indicators of source,and the relationships of phoscorites and carbonatites from the Kovdor massif,Kola peninsula,Russia

A detailed Sr−Nd isotopic study of primary apatite, calcite and dolomite from phoscorites and carbonatites of the Kovdor massif (380 Ma), Kola peninsula, Russia, reveals a complicated evolutionary history. At least six types of phoscorites and five types of carbonatite have been identified from Kovdor by previous investigators based on relative ages and their major and accessory minerals. Isotopic data from apatite define at least two distinct groups of phoscorite and carbonatite. Apatite from the earlier phoscorites and carbonatites (group 1) are characterized by relatively low⁸⁷Sr/⁸⁶Sr (0.70330–0.70349) and¹⁴³Nd/¹⁴⁴Nd initial ratios (0.51230–0.51240) with F=2.01–2.23 wt%, Sr=2185–2975 ppm, Nd=275–660 ppm and Sm=31.7–96.2 ppm. Apatite from the second group has higher⁸⁷Sr/⁸⁶Sr (0.70350–0.70363) and¹⁴³Nd/¹⁴⁴Nd initial ratios (0.51240–0.51247) and higher F (2.63–3.16 wt%), Sr (4790–7500 ppm), Nd (457–1074 ppm) and Sm (68.7–147.6 ppm) contents. This group corresponds to the later phoscorites and carbonatites. One apatite sample from a carbonatite from the earlier group fits into neither of the two groups and is characterized by the highest initial⁸⁷Sr/⁸⁶Sr (0.70385) and lowest¹⁴³Nd/¹⁴⁴Nd (0.51229) of any of the apatites. Within both groups initial⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios show negative correlations. Strontium isotope data from coexisting calcite and dolomite support the findings from the apatite study. The Sr and Nd isotopic similarities between carbonatites and phoscorites indicate a genetic relationship between the two rock types. Wide variations in Sr and Nd isotopic composition within some of the earlier carbonatites indicate several distinct intrusive phases. Oxygen isotopic data from calcite and dolomite (δ¹⁸O=+7.2 to +7.7‰ SMOW) indicate the absence of any low-temerature secondary processes in phoscorites and carbonatites, and are consistent with a mantle origin for their parental melts. Apatite data from both groups of phoscorite plot in the depleted quadrant of an ε_Nd versus ε_Sr diagram. Data for the earlier group lie along the Kola Carbonatite Line (KCL) as defined by Kramm (1993) and data from the later group plot above the KCL. The evolution of the phoscorites and carbonatites cannot be explained by simple magmatic differentiation assuming closed system conditions. The Sr−Nd data can best be explained by the mixing of three components. Two of these are similar to the end-members that define the Kola Carbonatite Line and these were involved in the genesis of the early phoscorites and carbonatites. An additional component is needed to explain the isotopic characteristics of the later group. Our study shows that apatite from rocks of different mineralogy and age is ideal for placing constraints on mantle sources and for monitoring the Sr−Nd evolution of carbonatites. Editorial responsibility: W. Schreyer     

Rare earth elements in phoscorites and carbonatites of the Devonian Kola Alkaline Province,Russia: Examples from Kovdor,Khibina, Vuoriyarvi and Turiy Mys complexes

The Devonian (ca. 385–360 Ma) Kola Alkaline Province includes 22 plutonic ultrabasic–alkaline complexes, some of which also contain carbonatites and rarely phoscorites. The latter are composite silicate–oxide–phosphate–carbonate rocks, occurring in close space-time genetic relations with various carbonatites. Several carbonatites types are recognized at Kola, including abundant calcite carbonatites (early- and late-stage), with subordinate amounts of late-stage dolomite carbonatites, and rarely magnesite, siderite and rhodochrosite carbonatites. In phoscorites and early-stage carbonatites the rare earth elements (REE) are distributed among the major minerals including calcite (up to 490 ppm), apatite (up to 4400 ppm in Kovdor and 3.5 wt.% REE₂O₃ in Khibina), and dolomite (up to 77 ppm), as well as accessory pyrochlore (up to 9.1 wt.% REE₂O₃) and zirconolite (up to 17.8 wt.% REE₂O₃). Late-stage carbonatites, at some localities, are strongly enriched in REE (up to 5.2 wt.% REE₂O₃ in Khibina) and the REE are major components in diverse major and minor minerals such as burbankite, carbocernaite, Ca- and Ba-fluocarbonates, ancylite and others. The rare earth minerals form two distinct mineral assemblages: primary (crystallized from a melt or carbohydrothermal fluid) and secondary (formed during metasomatic replacement). Stable (C–O) and radiogenic (Sr–Nd) isotopes data indicate that the REE minerals and their host calcite and/or dolomite have crystallized from a melt derived from the same mantle source and are co-genetic.     

Petrogenetic processes in the ultramafic, alkaline and carbonatitic magmatism in the Kola Alkaline Province: A review

Igneous rocks of the Devonian Kola Alkaline Carbonatite Province (KACP) in NW Russia and eastern Finland can be classified into four groups: (a) primitive mantle-derived silica-undersaturated silicate magmas; (b) evolved alkaline and nepheline syenites; (c) cumulate rocks; (d) carbonatites and phoscorites, some of which may also be cumulates. There is no obvious age difference between these various groups, so all of the magma-types were formed at the same time in a relatively restricted area and must therefore be petrogenetically related. Both sodic and potassic varieties of primitive silicate magmas are present. On major element variation diagrams, the cumulate rocks plot as simple mixtures of their constituent minerals (olivine, clinopyroxene, calcite, etc). There are complete compositional trends between carbonatites, phoscorites and silicate cumulates, which suggests that many carbonatites and phoscorites are also cumulates. CaO / Al₂O₃ ratios for ultramafic and mafic silicate rocks in dykes and pipes range up to 5, indicating a very small degree of melting of a carbonated mantle at depth. Damkjernites appear to be transitional to carbonatites. Trace element modelling indicates that all the mafic silicate magmas are related to small degrees of melting of a metasomatised garnet peridotite source. Similarities of the REE patterns and initial Sr and Nd isotope compositions for ultramafic alkaline silicate rocks and carbonatites indicate that there is a strong relationship between the two magma-types. There is also a strong petrogenetic link between carbonatites, kimberlites and alkaline ultramafic lamprophyres. Fractional crystallisation of olivine, diopside, melilite and nepheline gave rise to the evolved nepheline syenites, and formed the ultramafic cumulates. All magmas in the KACP appear to have originated in a single event, possibly triggered by the arrival of hot material (mantle plume?) beneath the Archaean/Proterozoic lithosphere of the northern Baltic Shield that had been recently metasomatised. Melting of the carbonated garnet peridotite mantle formed a spectrum of magmas including carbonatite, damkjernite, melilitite, melanephelinite and ultramafic lamprophyre. Pockets of phlogopite metasomatised lithospheric mantle also melted to form potassic magmas including kimberlite. Depth of melting, degree of melting and presence of metasomatic phases are probably the major factors controlling the precise composition of the primary melts formed.     

Geochemistry of radioactive elements in the rocks of the Guli Massif,Polar Siberia

The study of radioactive element distribution in the rocks of the Guli Complex revealed an increase of uranium and thorium contents in the final products of magmatic differentiation. In the carbonatite complex, the radioactive elements are mainly accumulated in the early rocks—phoscorites, while their contents in the late phases, dolomitic carbonatites, decrease. The Th/U ratio increases from near-chondritic values in the weakly differentiated highly-magnesian primary magmas to the late rocks—phoscorites, calcitic carbonatites, and dolomitic carbonatites. The majority of radioactive elements are hosted in rare-metal accessory minerals: perovskite, pyrochlore, calzirtite, and apatite. Rock-forming minerals are characterized by extremely low contents of radioactive elements.     

In situ LA-ICPMS Isotopic and Geochronological Studies on Carbonatites and Phoscorites from the Guli Massif,Maymecha-Kotuy,Polar Siberia

In this study we present a fresh isotopic data, as well as U–Pb ages from different REE-minerals in carbonatites and phoscorites of Guli massif using in situ LA-ICPMS technique. The analyses were conducted on apatites and perovskites from calcio-carbonatite and phoscorite units, as well as on pyrochlores and baddeleyites from the carbonatites. The ⁸⁷Sr/⁸⁶Sr ratios obtained from apatites and perovskites from the phoscorites are 0.70308–0.70314 and 0.70306–0.70313, respectively; and 0.70310–0.70325 and 0.70314–0.70327, for the pyrochlores and apatites from the carbonatites, respectively.Furthermore, the in situ laser ablation analyses of apatites and perovskites from the phoscorite yield εNd from 3.6 (±1) to 5.1 (±0.5) and from 3.8 (±0.5) to 4.9 (±0.5), respectively; εNd of apatites, perovskites and pyrochlores from carbonatite ranges from 3.2 (±0.7) to 4.9 (±0.9), 3.9 (±0.6) to 4.5 (±0.8) and 3.2 (±0.4) to 4.4 (±0.8), respectively. Laser ablation analyses of baddeleyites yielded an eHf(t)d of +8.5 (± 0.18); prior to this study Hf isotopic characteristic of Guli massif was not known. Our new in situ εNd, ⁸⁷Sr/⁸⁶Sr and eHf data on minerals in the Guli carbonatites imply a depleted source with a long time integrated high Lu/Hf, Sm/Nd, Sr/Rb ratios.In situ U–Pb age determination was performed on perovskites from the carbonatites and phoscorites and also on pyrochlores and baddeleyites from carbonatites. The co-existing pyrochlores, perovskites and baddeleyites in carbonatites yielded ages of 252.3 ± 1.9, 252.5 ± 1.5 and 250.8 ± 1.4 Ma, respectively. The perovskites from the phoscorites yielded an age of 253.8 ± 1.9 Ma. The obtained age for Guli carbonatites and phoscorites lies within the range of ages previously reported for the Siberian Flood Basalts and suggest essentially synchronous emplacement with the Permian-Triassic boundary.     

Decoupling of paired elements,crossover REE patterns,and mirrored spider diagrams: Fingerprinting liquid immiscibility in the Tapira alkaline–carbonatite complex,SE Brazil

Tapira is an alkaline silicate–carbonatite complex belonging to the kamafugite-carbonatite association in the Late-Cretaceous Alto Paranaíba Igneous Province (APIP). It is dominated by coarse-grained plutonic rocks (bebedourite – a phlogopite-, apatite-, and perovskite-rich clinopyroxenite – with subordinated dunites, wehrlites, carbonatites and phoscorites). The plutonic rocks are crosscut by fine-grained ultramafic alkaline rocks (phlogopite picrites, bebedouritic dikes) and fine-grained carbonatites. Both types of dike-rocks show petrographic evidence of the coexistence of immiscible silicate and carbonatite liquids, such as carbonate ocelli present in the silicate rocks and, more rarely, silicate ocelli within carbonatites. A detailed geochemical study of the rock types in the complex, with emphasis on the fine-grained varieties, showed that whilst some rocks may be related to each other through crystal fractionation (e.g. phlogopite picrites and bebedouritic dikes), others display anomalous trace-element behaviour that cannot be readily explained by the fractionation of a particular phase or combination of phases. We interpret such anomalous geochemical signatures as produced by silicate–carbonate liquid immiscibility, on the basis of available experimental data on partition coefficients between coexisting immiscible liquids. The immiscibility signatures comprise: (a) decoupling of geochemical pairs, such as Nb–Ta and Zr–Hf; (b) rotation of REE patterns, which cross over the patterns of the primitive liquids; and (c) matching and opposite enrichment-depletion trace elements relationships in spider diagrams of conjugate immiscible liquids. We suggest that, once established, such geochemical signatures are very difficult to erase during the subsequent petrogenetic evolution processes, which may result in superimposed conflicting signatures.     

Isotopic and Geochemical Investigation of the Chilwa Island Carbonatite Complex, Malawi: Evidence for a Depleted Mantle Source Region, Liquid Immiscibility, and Open-System Behaviour

Initial Nd, Pb, and Sr isotopic data from carbonatites and associatedintrusive silica-undersaturated rocks from the early Jurassic,Chilwa Island complex, located in southern Malawi, central Africa,suggest melt derivation from a Rb/Sr- and Nd/Sm-depleted butTh/Pb- and U/Pb-enriched mantle source. Initial ¹⁴³Nd/¹⁴⁴Nd(0.51265–0.51270) isotope ratios from the Chilwa Islandcarbonatites are relatively constant, but their initial ⁸⁷Sr/⁸⁶Sr(0.70319–0.70361) ratios are variable. The ¹⁸O_smow (9.53–14.15%0)and ¹³C_PDB (–3.27 to –1.50%0) isotope ratios ofthe carbonates are enriched relative to the range of mantlevalues, and there is a negative correlation between ¹⁸O andSr isotope ratios. The variations in Sr, C, and O isotopic ratiosfrom the carbonatites suggest secondary processes, such as interactionwith meteoric groundwater during late-stage carbonatite activity.The initial ¹⁴³Nd/¹⁴⁴Nd (0.51246 0.51269) and initial ⁸⁷Sr/⁸⁶Sr(0.70344–0.70383) isotope ratios from the intrusive silicaterocks are more variable, and the Sr more radiogenic than thosefrom the carbonatites. Most of the Pb isotope data from Chilwa Island plot to the rightof the geochron and close to the oceanic regression line definedby MORBs and OIBs. Initial Pb isotopic ratios from both carbonatites(²⁰⁷Pb/²⁰⁴Pb 15.63–15.71; ²⁰⁶Pb/²⁰⁴Pb 19.13–19.78)and silicate rocks (²⁰⁷Pb/²⁰⁴Pb 15.61–15.72; ²⁰⁶Pb/²⁰⁴Pb18.18–20.12) show pronounced variations, and form twogroups in Pb-Pb plots. The isotopic variations shown by Nd, Pb, and Sr for the ChilwaIsland carbonatites and intrusive silicates suggest that thesemelts underwent different evolutionary histories. The chemicaldata, including isotopic ratios, from the carbonatites and olivinenephelinites are consistent with magmatic differentiation ofa carbonated-nephelinite magma. A model is proposed in whichdifferentiation of the carbonatite magma was accompanied byfenitization (metasomatic alteration) of the country rocks bycarbonatite-derived fluids, and subsequent alteration of thecarbonatite by hydrothermal activity. The chemical and isotopicdata from the non-nephelinitic intrusive silicate rocks reveala more complex evolutionary history, involving either selectivebinary mixing of lower-crustal granulites and a nephelinitemagma, or incremental batch melting of a depleted source andsubsequent crustal contamination.     

Sr–Nd–Pb isotopic compositions of the Kovdor phoscorite–carbonatite complex, Kola Peninsula, NW Russia

The Sr, Nd and Pb isotopic compositions for the Kovdor phoscorite–carbonatite complex (PCC), Kola Peninsula, NW Russia, have been determined to characterize the mantle sources involved and to evaluate the relative contributions of a plume and subcontinental lithospheric mantle in the formation of the complex. The Kovdor PCC is a part of the Kovdor ultramafic–alkaline–carbonatite massif, and consists of six intrusions. The initial isotopic ratios of the analyzed samples, calculated at 380 Ma, display limited variations: ε_Nd, + 2.0 to + 4.7; ⁸⁷Sr/⁸⁶Sr, 0.70319 to 0.70361 (ε_Sr, − 12.2 to − 6.2); ²⁰⁶Pb/²⁰⁴Pb, 18.38 to 18.74; ²⁰⁷Pb/²⁰⁴Pb, 15.45 to 15.50; ²⁰⁸Pb/²⁰⁴Pb, 37.98 to 39.28. The Nd and Sr isotope data of the Kovdor PCC generally fit the patterns of the other phoscorites and carbonatites from the Kola Alkaline Province (KAP), but some data are slightly shifted from the mixing line defined as the Kola Carbonatite Line, having more radiogenic ⁸⁷Sr/⁸⁶Sr ratios. However, the less radiogenic Nd isotopic compositions and negative Δ7/4 values of Pb isotopes of the analyzed samples exclude crustal contamination, but imply the involvement of a metasomatized lithospheric mantle source. Isotopic variations indicate mixing of at least three distinct mantle components: FOZO-like primitive plume component, EMI-like enriched component and DMM-like depleted component. The isotopic nature of the EMI- and DMM-like mantle component observed in the Kovdor samples is considered to be inherited from metasomatized subcontinental lithospheric mantle. This supports the previous models invoking plume–lithosphere interaction to explain the origin of the Devonian alkaline carbonatite magmatism in the KAP.     

Geological structure and isotopic—geochronologic study of rocks from the Strel’na segment of the Terskii Greenstone belt,Kola Peninsula

The geological structure, age, and genesis of sedimentary—volcanogenic, metamorphic, and metasomatic rocks from the Terskii greenstone belt fringing the southern Imandra—Varzuga structure in the southeastern Kola Peninsula are discussed with defining main stages in endogenic activity of the region in the Late Archean and Early Proterozoic. The U-Pb method (SHRIMP-II, ID-TIMS, and Pb-LS techniques) was used to determine the age of volcano-sedimentary rocks of the Imandra Group as well as that of magmatic and superimposed metamorphic and metasomatic processes. The basic—intermediate metavolcanics of the Imandra Group are dated at 2.67 Ga, which corresponds to the Lopingian Gimol’skii Superhorizon (Late Archean). The Archean metavolcanics were subjected to Early Proterozoic regional metamorphism 2.1 Ga ago and metasomatic processes in the period of 1.85 to 1.77 Ga ago. The obtained data indicate multistage evolution of rock formation in the Terskii greenstone belt located in the southern flank of the Imandra—Varzuga structure in the Kola Peninsula.     

Unusual rocks and mineralisation in a new carbonatite complex at Kandaguba, Kola Peninsula, Russia

The paper presents the results from a reconnaissance investigation of carbonatites in a newly discovered alkaline complex in the Kola peninsula, Russia. The Kandaguba complex differs from other carbonatite plutons of the Kola alkaline province by (a) the absence of ultrabasic rocks, (b) widespread occurrence of nepheline-, cancrinite- and nepheline–cancrinite syenites and carbonatites and (c) presence of apatite–calcite ijolites and feldspar ijolites as separate intrusive phase. The Kandaguba carbonatites are notable for the predominance of late ferromagnesian varieties together with quartz and numerous accessory mineral species. The association of phosphates (monazite, gorseixite, goyazite, apatite), sulphides and tellurides (pyrite, sphalerite, galena, hessite), ilmenorutile, barite with quartz and ankerite is a remarkable feature of these carbonatites. The Kandaguba carbonatites are inferred to have been generated as the products of liquid immiscibility followed by differentiation of the carbonatite melt.     

Proterozoic Gremyakha-Vyrmes Polyphase Massif, Kola Peninsula: An example of mixing basic and alkaline mantle melts

The paper presents newly obtained data on the geological structure, age, and composition of the Gremyakha-Vyrmes Massif, which consists of rocks of the ultrabasic, granitoid, and foidolite series. According to the results of the Rb-Sr and Sm-Nd geochronologic research and the U-Pb dating of single zircon grains, the three rock series composing the massif were emplaced within a fairly narrow age interval of 1885 ± 20 Ma, a fact testifying to the spatiotemporal closeness of the normal ultrabasic and alkaline melts. The interaction of these magmas within the crust resulted in the complicated series of derivatives of the Gremyakha-Vyrmes Massif, whose rocks show evidence of the mixing of compositionally diverse mantle melts. Model simulations based on precise geochemical data indicate that the probable parental magmas of the ultrabasic series of this massif were ferropicritic melts, which were formed by endogenic activity in the Pechenga-Varzuga rift zone. According to the simulation data, the granitoids of the massif were produced by the fractional crystallization of melts genetically related to the gabbro-peridotites and by the accompanying assimilation of Archean crustal material with the addition of small portions of alkaline-ultrabasic melts. The isotopic geochemical characteristics of the foidolites notably differ from those of the other rocks of the massif: together with carbonatites, these rocks define a trend implying the predominance of a more depleted mantle source in their genesis. The similarities between the Sm-Nd isotopic characteristics of foidolites from the Gremyakha-Vyrmes Massif and the rocks of the Tiksheozero Massif suggest that the parental alkaline-ultrabasic melts of these rocks were derived from an autonomous mantle source and were only very weakly affected by the crust. The occurrence of ultrabasic foidolites and carbonatites in the Gremyakha-Vyrmes Massif indicates that domains of metasomatized mantle material were produced in the sublithospheric mantle beneath the northeastern part of the Fennoscandian Shield already at 1.88 Ga, and these domains were enriched in incompatible elements and able to produce alkaline and carbonatite melts. The involvement of these domains in plume-lithospheric processes at 0.4–0.36 Ga gave rise to the peralkaline melts that formed the Paleozoic Kola alkaline province.     

Carbonatite and Alkaline Magmatism in Taourirt (Morocco): Petrological, Geochemical and Sr-Nd Isotope Characteristics

Alkaline lamprophyre dykes from Taourirt (North Morocco) containnumerous xenoliths, ranging from alkaline pyroxenites, kaersutitites,gabbros and nepheline syenites to a calcite carbonatite. Thesilicate xenoliths and the host rocks consist of Al- and Ti-richdiopside–salite, mica or kaersutitite, ± nepheline,± plagioclase and K-feldspar, and ubiquitous apatite.Both the xenoliths and the lamprophyres are enriched in incompatibleelements. The chemical composition of the lamprophyres cannotbe accounted for by fractional crystallization alone. Moreover,the clinopyroxenes exhibit complex zoning, which requires repeatedmixing of pulses of more or less fractionated melts. The carbonatiteis a sövite cumulate with Sr-rich calcite, pyrochlore,fluorapatite, and rare salite. The Sr–Nd isotopic compositionsof the Taourirt rocks indicate a depleted mantle source, thecarbonatite having the most depleted composition, and definea linear trend similar to that of the East African carbonatites.The different rocks thus represent unrelated magmas, and thetrend is interpreted as mixing between two components with HIMUand EM1 mantle end-member signatures. An EM2 mantle componentcould also be involved for a few samples; it may correspondto hydrous metasomatized mantle of the PP–PKP (phlogopiteand phlogopite K-richterite peridotite) and MARID (mica, amphibole,rutile, ilmenite and diopside) type. KEY WORDS: alkaline magmatism; carbonatite; Morocco; REE; Sr–Nd isotopes     

Geochemical typification of kimberlite and related rocks of the North Anabar region,Yakutia

The results of geochemical typification of kimberlites and related rocks (alneites and carbonatites) of the North Anabar region are presented with consideration of the geochemical specification of their source and estimation of their potential for diamonds. The content of representative trace elements indicates the predominant contribution of an asthenospheric component (kimberlites and carbonatites) in their source, with a subordinate contribution of vein metasomatic formations containing Cr-diopside and ilmenite. A significant contribution of water-bearing potassium metasomatic parageneses is not recognized. According to the complex of geochemical data, the studied rocks are not industrially diamondiferous.     

Nd, Pb and Sr Isotopic Compositions of East African Carbonatites: Evidence for Mantle Mixing and Plume Inhomogeneity

New Pb isotopic data are presented for 10 young Mesozoic toCenozoic (0–116 Ma) carbonatites from a 1400 km long segmentof the East African Rift. Patterns observed in Pb vs Pb, Srvs Pb and Nd vs Pb isotope diagrams define unusual, nearly linear,trends that are interpreted as mixing between two componentsthat are broadly similar to the two mantle end-member components,HIMU and EM1, which were first recognized from ocean-islandbasalts. The two plutons with isotope signatures closest toHIMU and EM1 crop out within 140 km of each other. From thesedata, EM1 and HIMU are now known to occur in both continentaland oceanic settings that are associated with plumes or rifts.Moreover, these isotopic signatures tend to occur in regionswhere seismic tomography indicates prominent low-velocity zonesin the lower mantle. For these reasons, we favour a model forthe origin of the East African Rift carbonatites that involvesmelting and mixing of HIMU and EM1 components contained withinan isotopically heterogeneous mantle plume. We consider theHIMU and EM1 sources to be stored within the deep (lower 1000km) mantle, possibly the core–mantle boundary. The rolethat continental lithosphere plays in carbonatite generationis probably one of concentrating volatiles at the upper levelsof an ascending mantle plume. KEY WORDS: carbonatites; isotopes; rifts; plumes; FOZO     

Late Devonian Diamondiferous Kimberlite and Alkaline Picrite (Proto-kimberlite?) Magmatism in the Arkhangelsk Region, NW Russia

Widespread penecontemporaneous igneous activity affected NWRussia (the Kola Peninsula and adjoining areas to the SE aroundArkhangelsk) during the Late Devonian (360–380 Ma). Magmatismvaries from tholeiitic basalts, erupted in the axial regionsof former Middle Proterozoic (Riphean) rifts, to strongly alkalinerock-types on and marginal to Archaean cratons. NNE of Arkhangelskkimberlites, olivine lamproites and alkaline picrites were emplaced;all these rock-types are diamondiferous to varying extents.Higher TiO₂ (and also total Fe) distinguish predominantly mica-poorEastern Group kimberlites (TiO₂ = 2·4–3·1wt %) and spatially associated alkaline picrites (TiO₂ = 3·2–3·7wt %) from nearby micaceous Western Group kimberlites (TiO₂= 0·8–1·1 wt %). Each rock-type also hasdistinctive rare earth element (REE) patterns, and     

Carbonatite Magmatism and Plume Activity: Implications from the Nd, Pb and Sr Isotope Systematics of Oldoinyo Lengai

New Nd (0.51261–0.51268), Pb (²⁰⁶Pb/²⁰⁴Pb: 19.24–19.26),and Sr (0.70437–0.70446) isotopic compositions from tennatrocarbonatite lavas, collected in June 1993 from OldoinyoLengai, the only known active carbonatite volcano, are relativelyuniform, and are similar to data from the 1960 and 1988 flows.Three of the samples contain silicate spheroids, one of whichhas Nd and Sr isotopic ratios similar to host natrocarbonatite,consistent with an origin by liquid immiscibility or the mixingof melts with similar isotopic compositions. Pb isotope datafor two samples of trona are inconsistent with its involvementin the genesis of natrocarbonatite. New Pb isotope data fromsilicate volcanic and plutonic blocks (ijolite, nephelinite,phonolite, syenite) from Oldoinyo Lengai are highly variable(²⁰⁶Pb/²⁰⁴Pb, 17.75–19.34; ²⁰⁷Pb/²⁰⁴Pb, 15.41–15.67;²⁰⁸Pb/²⁰⁴Pb, 37.79–39.67), and define near-linear arraysin Pb-Pb diagrams. The isotopic data for the silicate rocksfrom Oldoinyo Lengai are best explained by invoking discretepartial melting events which generate undersaturated alkalinesilicate magmas with distinct isotopic ratios. Pb isotope ratiosfrom most ijolites and phonolites are predominantly lower andmore variable than from the natrocarbonatites, and are attributedto interaction between silicate melts involving HIMU and EMIsource components and an additional component, such as lower-crustalgranulites, DMM or PREMA (prevalent mantle). Variations in Nd,Pb and Sr isotope ratios from Oldoinyo Lengai, among the largestyet documented from a single volcano, are attributed to mantlesource heterogeneity involving mainly the mixing of HIMU andEMI mantle components. Based on the new isotopic data from OldoinyoLengai and data from other East African carbonatites, and mantlexenoliths, we propose a two-stage model in an attempt to explainthe isotope variations shown by carbonatites in this area. Themodel involves (I) the release of metasomatizing agents withHIMU-like signatures from upwelling mantle (‘plume’)source, which in turn metasomatize the sub-continental (old,isotopically enriched, EMI-like) lithosphere, and (2) variabledegrees and discrete partial melting of the resulting heterogeneous,metasomatized lithosphere. KEY WORDS: carbonatite; isotopes; Oldoinyo Lengai; mantle plumes ^*Telephone: (613) 788–2660, ext. 4419. Fax: (613) 788–4490. e-mail: kbell{at}ccs.carleton.ca     

Evolution of chemical composition of pyrochlore group minerals from phoscorites and carbonatites of the Khibina alkaline massif

Phoscorites and carbonatites of the Khibina alkaline massif, Russia contain three minerals of the pyrochlore group. They are, in order of crystallization: uranpyrochlore and pyrochlore in the phoscorites, and pyrochlore and bariopyrochlore in late calcite carbonatites. Early calcite carbonatites also contain uranpyrochlore and pyrochlore, but they are xenocrysts derived from the phoscorites. Alteration of the pyrochlore group minerals led to increasing U, Ti and water contents and decreasing Na, Ca, Nb and F contents. Crystallization of zoned uranpyrochlore to pyrochlore crystals in the phoscorites is explained by the experiments of Ryabchikov and Hamilton (1993, 1994) on the interaction of carbonate-phosphate melts with mantle peridotites.     

Source of parental melts to carbonatites–critical isotopic constraints

The restriction of most carbonatites to continental areas raises questions as to whether the parental liquids to carbonatites are generated within the continental lithosphere, or whether they are derived from deeper parts of the mantle with the lithosphere playing a subsidiary, but important, role in trapping volatile-rich melts/fluids. The constraints imposed by both radiogenic and stable isotopic data from carbonatites world-wide are consistent with a sub-lithospheric source for the parental melts, associated with either asthenospheric ‘upwellings’ or more deep-seated, plume-related activity. Crucial evidences that support the generation of carbonated melts from sub-lithospheric mantle are: the petrogenetic and temporal association of carbonatites with large igneous provinces (LIPs; e.g., Deccan, Parana), carbonatites with primitive noble gas isotopic signatures, radiogenic isotope ratios similar to OIBs (i.e. involving HIMU, EM1 and FOZO mantle components), and the uniform, time-integrated Rb/Sr and Sm/Nd development lines for Sr and Nd isotopic data for carbonatites from the Superior Province, Canada, and the Kola Peninsula, Russia. Such findings are difficult to reconcile with a lithospheric origin. Even if a metasomatized lithospheric mantle is considered to be the sole source of carbonated melts, an unknown mantle process is required, large enough to generate widespread, synchronous metasomatism spanning regions in excess of 1?×?10⁶?km².     

Petrology and geochemistry of peridotite xenoliths from the Letlhakane kimberlites, Botswana

The diamondiferous Letlhakane kimberlites are intruded into the Proterozoic Magondi Belt of Botswana. Given the general correlation of diamondiferous kimberlites with Archaean cratons, the apparent tectonic setting of these kimberlites is somewhat anomalous. Xenoliths in kimberlite diatremes provide a window into the underlying crust and upper mantle and, with the aid of detailed petrological and geochemical study, can help unravel problems of tectonic setting. To provide relevant data on the deep mantle under eastern Botswana we have studied peridotite xenoliths from the Letlhakane kimberlites. The mantle-derived xenolith suite at Letlhakane includes peridotites, pyroxenites, eclogites, megacrysts, MARID and glimmerite xenoliths. Peridotite xenoliths are represented by garnet-bearing harzburgites and lherzolites as well as spinel-bearing lherzolite xenoliths. Most peridotites are coarse, but some are intensely deformed. Both garnet harzburgites and garnet lherzolites are in many cases variably metasomatised and show the introduction of metasomatic phlogopite, clinopyroxene and ilmenite. The petrography and mineral chemistry of these xenoliths are comparable to that of peridotite xenoliths from the Kaapvaal craton. Calculated temperature-depth relations show a well-developed correlation between the textures of xenoliths and P-T conditions, with the highest temperatures and pressures calculated for the deformed xenoliths. This is comparable to xenoliths from the Kaapvaal craton. However, the P-T gap evident between low-T coarse peridotites and high-T deformed peridotites from the Kaapvaal craton is not seen in the Letlhakane xenoliths. The P-T data indicate the presence of lithospheric mantle beneath Letlhakane, which is at least 150 km thick and which had a 40mW/m² continental geotherm at the time of pipe emplacement. The peridotite xenoliths were in internal Nd isotopic equilibrium at the time of pipe emplacement but a lherzolite xenolith with a relatively low calculated temperature of equilibration shows evidence for remnant isotopic disequilibrium. Both harzburgite and lherzolite xenoliths bear trace element and isotopic signatures of variously enriched mantle (low Sm/Nd, high Rb/Sr), stabilised in subcontinental lithosphere since the Archaean. It is therefore apparent that the Letlhakane kimberlites are underlain by old, cold and very thick lithosphere, probably related to the Zimbabwe craton. The eastern extremity of the Proterozoic Magondi Belt into which the kimberlites intrude is interpreted as a superficial feature not rooted in the mantle. Received: 19 March 1996 / Accepted: 16 October 1996