The Catoca kimberlite pipe, Republic of Angola: A paleovolcanological model

The Catoca kimberlite pipe is among the world’s largest primary diamond deposits. The Catoca volcanic edifice is only slightly eroded. Kimberlitic rocks of various facies compose a crater of about 1 km in diameter and a diatreme. The structure of the pipe and mining conditions of the deposit are complicated by intense intrapipe tectonic processes related to large-amplitude subsidence. Based on geological data, we propose a structural model of the deposit and a paleovolcanological model of the Catoca pipe formed during a full cycle beginning with a stage of active volcanism and completed by stages of gradually waning volcanic activity and sedimentation. It is suggested that the banded tuffisitic kimberlite of the crater zone was deposited at the stage of active volcanic eruption from specific pyroclastic suspension as a low-viscosity mixture of crystals and aqueous sol rich in serpentine.     

Morphology of diamonds from kimberlite pipes of the Catoca field, Angola

The paper presents new data on the morphology of more than 3200 diamond crystals from kimberlite pipes of the Catoca field located in the Lunda diamond-bearing province of northeastern Angola. The diamond crystals from particular pipes of this field differ in their morphology and their physical and mineralogical properties. Octahedrons are predominant in the morphological spectrum of crystals from the Catoca and Kamitongo pipes, indicating more favorable conditions for diamond growth and preservation in comparison with diamonds from the Kakele pipe, where rhombic dodecahedrons are prevalent. In general, morphological and other mineralogical features of diamond crystals may be used in appraisal of the diamond-bearing potential of their primary sources in northeastern Angola.     

Petrology of two diamondiferous eclogite xenoliths from the Lahtojoki kimberlite pipe, eastern Finland

Diamondiferous Group A eclogites constitute a minor portion of the mantle-derived xenoliths in the eastern Finland kimberlites. They have been derived from the depth interval 150–230 km where they are inferred to occur as thin layers or small pods within coarse-grained garnet peridotites. The chemical and isotopic composition of minerals suggest that they represent (Proterozoic?) mantle-derived melts or cumulates rather than subducted oceanic lithosphere. During magma ascent and emplacement of the kimberlites, the eclogite xenoliths were mechanically and chemically rounded judging from the types of surface markings. In addition, those octahedral crystal faces of diamonds that were partially exposed from the rounded eclogite xenolith became covered by trigons and overlain by microlamination due to their reaction with the kimberlite magma. The diamonds bear evidence of pervasive plastic deformation which is not, however, evident in the eclogite host. This suggests that annealing at ambient lithospheric temperatures has effectively recrystallised the silicates while the diamond has retained its lattice imperfections and thus still has the potential to yield information about ancient mantle deformation. One of our samples is estimated to contain approximately 90,000 ct/ton diamond implying that some diamonds occur within very high-grade pods or thin seams in the lithospheric mantle. To our knowledge, this is one of the most diamondiferous samples described.     

Multi-stage metasomatism of diamondiferous eclogite xenoliths from the Udachnaya kimberlite pipe,Yakutia, Siberia

The primary garnet (pyrope-almandine)-omphacite (Cpx 1, 6.5–7 wt% Na₂O)-sulfide (Fe-Ni-Co mss) assemblage of the two diamondiferous eclogite xenoliths studied (U33/1 and UX/1) experienced two mantle metasomatic events. The metasomatic event I is recorded by the formation of platy phlogopite (~ 10 wt% K₂O), prior to incorporation of the xenoliths in the kimberlite. The bulk of the metasomatic alteration, consisting of spongy-textured clinopyroxene (Cpx 2A, 1–3 wt% Na₂O), coarser-grained clinopyroxene (Cpx 2B, 2–5 wt% Na₂O), pargasitic amphibole (~ 0.8 wt% K₂O; 3–3.5 wt% Na₂O), kelyphite (Cpx 3, mostly <1 wt% Na₂O; and zoned Mg-Fe-Al spinel), sodalite, calcite, K-feldspar, djerfisherite (K_5.95Na_0.02Fe_18.72Ni_2.36Co_0.01Cu_4.08S₂₆Cl ) and a small amount of K-Ca-Fe-Mg glass, is ascribed to the metasomatic event II that occurred also in the upper mantle, but after the xenoliths were incorporated in the kimberlite. A pervasive chloritic alteration (mainly clinochlore + magnetite) that overprints earlier assemblages probably took place in the upper crustal environment. The diamonds are invariably associated with secondary clinopyroxene and chlorite, but the diamonds formed before the entrainment of the xenoliths in the Udachnaya kimberlite.Editorial Responsibility: T.L. Grove     

Two diamond-bearing peridotite xenoliths from the finsch kimberlite,South Africa

Two diamond bearing xenoliths found at Finsch Mine are coarse garnet lherzolites, texturally and chemically similar to the dominant mantle xenoliths in that kimberlite. A total of 46 diamonds weighing 0.053 carats have been recovered from one and 53 diamonds weighing 0.332 carats from the other. The diamonds are less corroded than diamonds recovered from the kimberlite. Geothermobarometric calculations indicate that the xenoliths equilibrated at 1,130° C and pressures 50 kb which is within the diamond stability field; this corresponds to depths of 160 km and would place the rocks on a shield geotherm at slightly greater depths than most coarse garnet lherzolites from kimberlite. The primary minerals in the two rocks are very similar to each other but distinctly different to the majority of mineral inclusions in Finsch diamonds. This suggests a different origin for the diamonds in the kimberlite and the diamonds in the xenoliths although the equilibration conditions for both suites are approximately coincident and close to the wet peridotite solidus.     

Mineralogy of the upper mantle: A review of the minerals in mantle xenoliths from kimberlite

The importance of ultramafic and eclogitic xenoliths in kimberlite as representing the rocks and minerals of the upper mantle has been widely perceived during the last decade. Studies of the petrology and mineral chemistry of these mantle fragments as well as of inclusions in diamond, have led to significant progress in our understanding of the mineralogy and chemistry of the upper mantle. For example, it is now known that textural differences in the ultramafic xenoliths (lherzolite, harzburgite, pyroxenite and websterite) are partially reflected in chemical differences. Thus xenoliths that display a ‘fluidal’ texture, indicative of intense deformation are less depleted in Ca, Al, Na, Fe and Ti than those xenoliths in which granular textures are predominant. It is believed this relative depletion may indicate the sheared (fluidal texture) xenoliths are representative of primary, undifferentiated mantle. This material on partial melting would produce ‘basaltic-type’ material, and leave a residuum whose chemistry and mineralogy is reflected by the granular xenoliths.Also present in kimberlite are large single phase xenoliths that may be either one single crystal (xenocryst, megacryst) or an aggregate of several crystals of the same mineral (discrete xenolith, or discrete nodule). These large single phase samples consist of similar minerals to those occurring in the ultramafic xenoliths but chemically they are distinct in being generally more Fe-rich. The relation between these xenocrysts to their counterparts in the ultramafic xenoliths is unknown. Also unknown, at the present time, is the exact relation between diamond and kimberlite. Evidence obtained from study of the mineral inclusions in diamond suggests that diamond forms in at least two chemically distinct environments in the mantle; one eclogitic, the other, ultramafic. Interestingly, this suggestion is true for diamonds from worldwide localities.The mineral-chemical results of studies on xenoliths and inclusions in diamond have been convincingly interpreted in the light of experimental studies. It is now possible based on several different geothermometers and barometers to determine relatively reasonable physical conditions for the final genesis of many of these mantle rocks. For the most part the final equilibration temperatures range between 1000 and 1400°C and pressure in the region 100–200 km. These conditions are consistent with an upper mantle origin. Future studies will undoubtedly attempt to more concisely, and accurately, define these conditions, as well as understand better the chemical and spatial relationship of the rock-types in the mantle.     

Interaction between protokimberlite melts and mantle lithosphere: Evidence from mantle xenoliths from the Dalnyaya kimberlite pipe,Yakutia (Russia)

The Dalnyaya kimberlite pipe(Yakutia,Russia) contains mantle peridotite xenoliths(mostly Iherzolites and harzburgites) that show both sheared porphyroclastic(deformed) and coarse granular textures,together with ilmenite and clinopyroxene megacrysts.Deformed peridotites contain high-temperature Fe-rich clinopyroxenes,sometimes associated with picroilmenites,which are products of interaction of the lithospheric mantle with protokimberlite related melts.The orthopyroxene-derived geotherm for the lithospheric mantle beneath Dalnyaya is stepped similar to that beneath the Udachnaya pipe.Coarse granular xenoliths fall on a geotherm of 35 mWm-2 whereas deformed varieties yield a 45 mWm-2)geotherm in the 2-7.5 GPa pressure interval.The chemistry of the constituent minerals including garnet,olivine and clinopyroxene shows trends of increasing Fe~#(=Fe/(Fe+Mg))with decreasing pressure.This may suggest that the interaction with fractionating protokimberlite melts occurred at different levels.Two major mantle lithologies are distinguished by the trace element patterns of their constituent minerals,determined by LA-ICP-MS.Orthopyroxenes,some clinopyroxenes and rare garnets are depleted in Ba,Sr,HFSE and MREE and represent relic lithospheric mantle.Re-fertilized garnet and clinopyroxene are more enriched.The distribution of trace elements between garnet and clinopyroxene shows that the garnets dissolved primary orthopyroxene and clinopyroxene.Later high temperature clinopyroxenes related to the protokimberlite melts partially dissolved these garnets.Olivines show decreases in Ni and increases in Al,Ca and Ti from Mg-rich varieties to the more Fe-rich,deformed and refertilized ones.Minerals showing higher Fe~#(0.11-0.15) are found within intergrowths of low-Cr ilmenite-clinopyroxene-garnet related to the crystallization of protokimberlite melts in feeder channels.In P-f(O_2) diagrams,garnets and Cr-rich clinopyroxenes indicate reduced conditions at the base of the lithosphere at-5 log units below a FMQ buffer.However,Cr-poor clinopyroxenes,together with ilmenite and some Fe-Ca-rich garnets,demonstrate a more oxidized trend in the lower part of lithosphere at-2 to 0 log units relative to FMQ.Clinopyroxenes from xenoliths in most cases show conditions transitional between those determined for garnets and megacrystalline Cr-poor suite.The relatively low diamond grade of Dalnyaya kimberlites is explained by a high degree of interaction with the oxidized protokimberlite melts,which is greater at the base of the lithosphere.     

Pyrope-spinel (alkremite) xenoliths from kimberlite

Xenoliths consisting of two thirds pyrope (Py₇₃Alm₁₄Gr₁₃-Py₁₅Alm₁₈Gr₃₁) and one third hercynite-bearing spinel with minor chromium, from Bellsbank and Jagersfontein kimberlites, South Africa, are compared with similar rocks, alkremites, from the Udachnaya pipe, U.S.S.R. From published experimental data and textural relationships these formed as early dense cumulates in aluminous mantle melts under restricted pressure conditions equivalent to about 75 km depth. At greater pressures very pyrope-rich garnets (Py₈₀) are capable of being formed. The garnet spinel xenoliths are considered to have become separated from the magma prior to crystallisation of clinopyroxene, whereas complete uninterrupted fractionation and reaction would produce the more common griquaites (eclogites).     

A study of garnets from eclogite and peridotite xenoliths found in kimberlite

The chemical compositions of garnets from 58 eclogite, 72 peridotite and 4 pyroxenite xenoliths in kimberlites have been estimated from their unit cell edge length and refractive indices. The samples studied were obtained from 17 kimberlite occurrences and include all those of known source which remain in the famous Williams (1932) collection which is stored at the University of Cape Town. Every suitable sample available to the authors has been examined.A gap in the range of garnet volume percentages occurs in the samples studied between approximately 15 and 30%. Garnet peridotites characteristically have <15% garnet and eclogites >30% garnet. Very rare exceptions occur. Our collection contains no eclogites with olivine and only one with orthopyroxene. All but two of the peridotite-pyroxenite group contain orthopyroxene. The garnets from the peridotites and pyroxenites plot on a pyrope-almandine-uvarovite triangle in a narrow band with a remarkably constant almandine/uvarovite ratio. Garnets from the eclogites are plotted on a pyrope-almandine-grossularite triangle and have a wide spread of compositions. These fall into 4 groups viz. eclogite I, eclogite II, kyanite eclogite and corundum eclogite.The reasons for the differences in garnet chemistry are considered and a tentative evolutionary scheme suggested by partial melting of the garnet peridotite which is assumed to occur in the upper mantle. Recent models of upper mantle composition and the genesis of garnet-bearing xenoliths in kimberlite are briefly and critically examined.S.A. UMP Publication No. 9.     

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.     

Graphite- and diamond-bearing eclogite xenoliths from the Bellsbank kimberlites,Northern Cape,South Africa

 One diamond-bearing and eight graphite-bearing eclogite xenoliths are described from the Bellsbank kimberlites, Cape Province, South Africa. Graphite mostly occurs as discrete grains which are commonly in the form of tabular prisms. Diamond is octahedral. Both Group I and Group II eclogite varieties are represented by the graphite-bearing specimens, while the single diamond-bearing eclogite is of the Group I variety. The carbon isotopic composition of the graphite varies from δ¹³C=−7‰ to δ¹³C=−2.8‰. This is within the range of carbon isotopic compositions for inclusion-free diamonds in kimberlite from this locality, suggesting that the carbon for the eclogites as well as some of the kimberlite diamonds are derived from the same source. The present day Nd isotopic compositions of clinopyroxene from three graphite-bearing xenoliths are slightly higher than the bulk earth estimate. Sr isotopic compositions of the clinopyroxene in these xenoliths vary from ⁸⁷Sr/⁸⁶Sr=0.703 to ⁸⁷Sr/⁸⁶Sr=0.706. This could be due to derivation of the xenoliths from a protolith with variable ⁸⁷Sr/⁸⁶Sr isotopic composition or could be the result of mixing between a low-Sr, high ⁸⁷Sr/⁸⁶Sr component and a high Sr, low ⁸⁷Sr/⁸⁶Sr component. Received: 1 June 1994/Accepted: 6 March 1995     

Hydroxyl in mantle olivine xenocrysts from the Udachnaya kimberlite pipe

The incorporation of hydrogen in mantle olivine xenocrysts from the Udachnaya kimberlite pipe was investigated by Fourier-transform infrared spectroscopy and secondary ion mass spectrometry (SIMS). IR spectra were collected in the OH stretching region on oriented single crystals using a conventional IR source at ambient conditions and in situ at temperatures down to −180°C as well as with IR synchrotron radiation. The IR spectra of the samples are complex containing more than 20 strongly polarized OH bands in the range 3,730–3,330 cm⁻¹. Bands at high energies (3,730–3,670 cm⁻¹) were assigned to inclusions of serpentine, talc and the 10 Å phase. All other bands are believed to be intrinsic to olivine. The corresponding point defects are (a) associated with vacant Si sites (3,607 cm⁻¹ E || a, 3,597 E || a, 3,571 cm⁻¹ E || c, 3,567 E || c, and 3,556 E || b), and (b) with vacant M1 sites (most of the bands polarized parallel to a). From the pleochroic behavior and position of the OH bands associated with the vacant M1 sites, we propose two types of hydrogen—one bonded to O1 and another to O2, so that both OH vectors are strongly aligned parallel to a. The O2–H groups may be responsible for the OH bands at higher wavenumbers than those for the O1–H groups. The multiplicity of the corresponding OH bands in the spectra can be explained by different chemical environments and by slightly different distortions of the M1 sites in these high-pressure olivines. Four samples were investigated by SIMS. The calculated integral molar absorption coefficient using the IR and SIMS results of 37,500±5,000 L mol H₂O cm⁻² is within the uncertainties slightly higher than the value determined by Bell et al. (J Geophys Res 108(B2):2105–2113, 2003) (28,450±1,830 L mol H₂O cm⁻²). The reason for the difference is the different distributions of the absorption intensity of the spectra of both studies (mean wavenumber 3,548 vs. 3,570 cm⁻¹). Olivine samples with a mean wavenumber of about 3,548 cm⁻¹ should be quantified with the absorption coefficient as determined in this study; those containing more bands at higher wavenumber (mean wavenumber 3,570 cm⁻¹) should be quantified using the value determined by Bell et al. (J Geophys Res 108(B2):2105–2113, 2003).

Water content in minerals of mantle xenoliths from the Udachnaya pipe kimberlites (Yakutia)

Distribution of water among the main rock-forming nominally anhydrous minerals of mantle xenoliths of peridotitic and eclogitic parageneses from the Udachnaya kimberlite pipe, Yakutia, has been studied by IR spectroscopy. The spectra of all minerals exhibit vibrations attributed to hydroxyl structural defects. The content of H₂O (ppm) in minerals of peridotites is as follows: 23–75 in olivine, 52–317 in orthopyroxene, 29–126 in clinopyroxene, and 0–95 in garnet. In eclogites, garnet contains up to 833 ppm H₂O, and clinopyroxene, up to 1898 ppm (~ 0.19 wt.%). The obtained data and the results of previous studies of minerals of mantle xenoliths show wide variations in H₂O contents both within different kimberlite provinces and within the Udachnaya kimberlite pipe. Judging from the volume ratios of mineral phases in the studied xenoliths, the water content varies over narrow ranges of values, 38–126 ppm. At the same time, the water content in the studied eclogite xenoliths is much higher and varies widely, 391–1112 ppm.     

Petrology and geochemistry of eclogite xenoliths from the Rietfontein kimberlite,Northern Cape,South Africa

Petrographic and geochemical features of a suite of eclogite xenoliths from the Rietfontein kimberlite that erupted through probable Proterozoic crust west of the Kaapvaal Craton in the far Northern Cape region of South Africa, are described. Group II eclogites dominate the suite both texturally and chemically, but can be subdivided into bimineralic, opx-bearing and kyanite-bearing groups. Temperature estimates from different geothermometers range from 700 to 1,000°C, indicating derivation from relatively shallow mantle depths. Orthopyroxene-bearing eclogites are inferred to originate from depths of 85 to 115 km and lie close to the average cratonic thermal profile for southern Africa. These uppermost mantle temperatures during the late Cretaceous provide evidence for equilibration of the off-craton lithosphere to craton-like thermal conditions following Namaqua-Natal orogenesis. The kyanite eclogites are distinct from the remaining eclogites in terms of both major and trace element compositions and their lesser degree of alteration. Garnets are richer in Ca, and are Cr-depleted relative to garnets from the bimineralic and opx-bearing eclogites, which tend to be more magnesian. Clinopyroxenes from the kyanite eclogites are more sodic, with higher Al₂O₃ and lower MgO contents than the bimineralic and opx-bearing eclogites. LREE-depletion, positive Sr and Eu anomalies, and the Al-rich, Si-poor bulk composition suggest a plagioclase-rich, probably troctolitic protolith for the kyanite eclogites. In contrast, the major and trace element bulk compositions of the high-MgO bimineralic and orthopyroxene-bearing eclogites are consistent with gabbroic or pyroxenitic precursors, or high-pressure cumulates, rather than mafic to ultramafic lavas. δ¹⁸O values for garnets do not deviate significantly from typical mantle values. The observations reported do not discriminate unambiguously between continental and oceanic origins for the various eclogite components in the mantle lithosphere of this region.