Post-emplacement serpentinization and related hydrothermal metamorphism in a kimberlite from Venetia, South Africa

The common serpentine–diopside matrix assemblage in volcaniclastic kimberlite (VK) at the Venetia Mine, South Africa is ascribed to a secondary origin, because of post‐emplacement serpentinization and associated hydrothermal metamorphism. Volcaniclastic deposits with 20–30% porosity infill kimberlite pipes in the waning stages of kimberlite eruptions. Olivine macrocrysts are typically rimmed by talc and are pseudomorphed by lizardite, with minor magnetite. The fine matrix consists of mixtures of lizardite, chlorite, smectite, brucite, calcite, titanite and andradite, an assemblage which either pseudomorphed microcrysts or in‐filled voids. Locally we recognize microcryst pseudomorphs rich in sub‐microscopic mixtures of lizardite with smectite, and other microcryst pseudomorphs and void‐filling matrix rich in chlorite and lizardite. Interstitial lizardite and associated phyllosilicates (brucite, smectite and chlorite) crystallized progressively from meteoric or hydrothermally derived pore waters, and Si⁴⁺ and Mg²⁺ released into the fluid phase during serpentinization of olivine macrocrysts. Radial‐fibrous fringes of diopside microlites around crystals display void‐filling textures because of unrestricted growth into pore spaces. Secondary diopside is attributed to Si⁴⁺, Mg²⁺ and Ca²⁺ cations released into the fluid phase by interaction with olivine, calcite and plagioclase in siliceous xenoliths. The paucity of primary, fine‐grained groundmass phases resistant to alteration, for example, perovskite and spinel, precludes an origin for the intergrain matrix as altered interstitial ash, glass or a late‐stage kimberlite melt. Isovolumetric replacement of olivine results in a volume increase of 60% so that pore spaces in the original deposit can be easily filled up with serpentine. The source of Al³⁺ to form chlorite and smectite is attributed to alteration of plagioclase in xenoliths which comprise 20–30 vol.% of the deposit. Titanite, hydro‐andradite and second‐generation diopside precipitate as hydrothermal minerals from calcium‐bearing serpentinizing fluids in replacement reactions and as void‐filling minerals. Consideration of mineral equilibria in the CaO‐MgO‐SiO₂‐H₂O‐CO₂ system constrains the common matrix assemblage of lizardite and diopside in X_CO2)–T space. At 300 bar, the assemblage is stable only at temperatures below 370 °C and X_CO2 < 0.01. This upper limit on temperature is well below the plausible solidus of ultrabasic magmas. Furthermore, the requirement of trace CO₂ in the fluid phase implies a post‐emplacement external source rather than ‘autometamorphism’ from kimberlite‐derived fluids, because of high P_CO2 commonly inferred for kimberlite magmas.     

Gabbroic xenoliths in tuff-breccia pipes from the Hyblean Plateau: insights into the nature and composition of the lower crust underneath South-eastern Sicily, Italy

Summary Crust-derived xenoliths hosted by Miocene basaltic diatremes in the Hyblean Plateau (south-eastern Sicily, Italy) provide new information regarding the nature of a portion of the central Mediterranean lower crust. These xenoliths can be divided into three groups: gabbros (plagioclase + clinopyroxene + Fe–Ti oxides ± apatite ± amphibole ± Fe-rich green spinel), diorites (An-poor plagioclase, clinopyroxene ± Fe–Ti oxides ± orthopyroxene) and mafic granulites (plagioclase + clinopyroxene + green spinel ± orthopyroxene ± Fe–Ti oxides). Gabbros form the main subject of this paper. They represent cumulates whose igneous texture has been locally obliterated by metamorphic recrystallization and shearing. They were permeated by Fe–Ti-rich melts related to tholeiitic-type fractional crystallisation. Incompatible element ratios (Zr/Nb = 5–26; Y/Nb = 1.4–11) indicate that these cumulate gabbros derived from MORB liquids. Late-stage and hydrothermal fluids caused diverse, sometimes important, metasomatic trasformations. Petrographic and geochemical comparison with gabbroids from well-known geodynamic settings show that the Hyblean lower crustal xenoliths were probably formed in an oceanic or oceanic-continent transition environment.     

Highly evolved hypabyssal kimberlite sills from Wemindji,Quebec, Canada: insights into the process of flow differentiation in kimberlite magmas

Kimberlite sills emplaced in granite located near the town of Wemindji (Quebec, Canada) range from 2 cm to 1.2 m in thickness. The sills exhibit a wide variation in macroscopic appearance from fine-grained aphanitic dolomitic hypabyssal kimberlite to ilmenite/garnet macrocrystal hypabyssal kimberlite. Diatreme or crater facies rocks are not present. Multiple intrusions are present within the sills, and graded bedding and erosional features such as cross-bedding are common. The sills exhibit a wide range in their modal mineralogy with respect to the abundances of spinel, apatite, phlogopite and dolomite. Olivine is the dominant macrocryst, with an average composition of Fo₉₀. Garnet macrocrysts are low chrome (2–3 wt. %) pyrope (G1/G9 garnet). Ilmenite occurs as rounded macrocrysts (7–13 wt. % MgO). Phlogopite microphenocrysts are Ti-poor and represent a solid solution between phlogopite and kinoshitalite end members. Spinel compositions mainly represent the Cr-poor members of the qandilite–ulvöspinel–magnetite series. The principle carbonate comprising the groundmass is dolomite, with lesser later-forming calcite. Accessory minerals include apatite, Sr-rich calcite, Nb-rich rutile, baddeleyite, monazite-(Ce) and barite. While some of these accessory minerals are atypical of kimberlites in general, it is expected that differentiation products of an evolved carbonate-rich kimberlite magma will crystallize these phases. The Wemindji kimberlites offer insight into the process of crystal fractionation and differentiation in evolved kimberlite magmas. The macroscopic textural features observed in the Wemindji sills are interpreted to represent flow differentiation of a mantle-derived, very fluid, low viscosity carbonate-rich kimberlite. The diverse modes and textural features result entirely from flow differentiation and multiple intrusions of different batches of genetically related kimberlite magma. The mineralogy of the Wemindji kimberlites has some similarities to that of the Wesselton and Benfontein calcite kimberlite sills but differs in detail with respect to dominant carbonate (i.e. dolomite versus calcite), and the character of the rare earth-bearing accessory minerals (i.e. monazite-(Ce) versus rare earth fluorocarbonates).     

Geology of the Gahcho Kué kimberlite pipes, NWT, Canada: root to diatreme magmatic transition zones

The Cambrian Gahcho Kué kimberlite cluster includes four main pipes that have been emplaced into the Archaean basement granitoids of the Slave Craton. Each of the steep-sided pipes were formed by the intrusion of several distinct phases of kimberlite in which the textures vary from hypabyssal kimberlite (HK) to diatreme-facies tuffisitic kimberlite breccia (TKB). The TKB displays many diagnostic features including abundant unaltered country rock xenoliths, pelletal lapilli, serpentinised olivines and a matrix composed of microlitic phlogopite and serpentine without carbonate. The HK contains common fresh olivine set in a groundmass composed of monticellite, phlogopite, perovskite, serpentine and carbonate. A number of separate phases of kimberlite display a magmatic textural gradation from TKB to HK, which is characterised by a decrease in the proportion of pelletal lapilli and country rock xenoliths and an increase in groundmass crystallinity, proportion of fresh olivine and the degree of xenolith digestion.

The pipe shapes and infills of the Gahcho Kué kimberlites are similar to those of the classic South African pipes, particularly those of the Kimberley area. Similar intrusive magmatic emplacement processes are proposed in which the diatreme-zone results from the degassing, after breakthrough, of the intruding magma column. The transition zones represent ‘frozen’ degassing fronts. The style of emplacement of the Gahcho Kué kimberlites is very different from that of many other pipes in Canada such as at Lac de Gras, Fort à la Corne or Attawapiskat.     

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     

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.     

Spinel-facies mantle xenoliths from Cerro Redondo, Argentine Patagonia: Petrographic, geochemical, and isotopic evidence of interaction between xenoliths and host basalt

Cerro Redondo is an ancient cinder cone now almost completely eroded, sited over a sill that corresponds to a sub-volcanic magma chamber, in Santa Cruz province, Patagonia, Argentina. It is composed of Pliocene-Pleistocene alkaline basalt containing spinel-facies lherzolite and harzburgite mantle xenoliths. Core compositions of pyroxenes indicate temperatures of 823 °C to 1043 °C and pressures of 12.4 kb to 21.4 kb. Based on P–T estimates, petrographic, geochemical, and isotopic characteristics, we propose that Cerro Redondo xenoliths come from a thick homogeneous mantle column (36 km to 63 km depth), and present different degrees of basalt infiltration. A simple mixing model based on Sr isotopes was used to quantify the host basalt infiltration, and contamination values of 0.0%, 0.2%, 3%, and 12% were obtained for samples X-F, X-D, X-C, and X-B, respectively. For unknown reasons, samples X-G and X-E suffered selective isotopic and trace element modification, respectively, associated with 1% of basalt infiltration. Sample X-F best represents the sub-continental lithospheric mantle column, conserving primary equilibrium textures with sharp grain boundaries, and having TiO₂, CaO, Na₂O, K₂O, and P₂O₅ contents lower than average spinel lherzolite, flat chondrite-normalized REE pattern, and ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios of 0.70519 and 0.51297, respectively. This sample records a decoupling of the Sr–Nd system where Sr ratios increase at constant Nd ratios, possibly caused by chromatographic processes. Its ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios are 17.987, 15.556, and 37.959, respectively. As the interaction with the host basalt increases, xenoliths show a gradual increase of disequilibrium textures such as reaction rims and exsolution lamellae in orthopyroxene and clinopyroxene, and increase of TiO₂, CaO, Al₂O₃, Na₂O, K₂O, P₂O₅, LREE, and incompatible element concentrations. The Sr–Nd system shows an unusual positive trend from the unmodified sample X-F toward the host basalt isotope composition with ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios of 0.70447 and 0.51279, respectively, while ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios tend to increase toward those of the host basalt (18.424, 15.648, and 38.728, respectively) as the xenolith–basalt interaction increases. The basalt–xenolith reaction probably started during the transport of the xenoliths to the surface, and continued during the residence of xenoliths in the sub-volcanic magma chamber of Cerro Redondo.     

Megacrysts and xenoliths in kimberlite,Elliott County,Kentucky: A mantle sample from beneath the Permian Appalachian Plateau

Two kimberlite pipes in Elliott County contain rare ultramafic xenoliths and abundant megacrysts of olivine (Fo_85–93), garnet (0.21–9.07% Cr₂O₃), picroilmenite, phlogopite, Cr-poor clinopyroxene (0.56–0.88% Cr₂O₃), and Cr-poor orthopyroxene (<0.03–0.34% Cr₂O₃) in a matrix of olivine (Fo_88–92), picroilmenite, Cr-spinel, magnetite, perovskite, pyrrhotite, calcite, and hydrous silicates. Rare clinopyroxene-ilmenite intergrowths also occur. Garnets show correlation of mg (0.79–0.86) and CaO (4.54–7.10%) with Cr₂O₃ content; the more Mg-rich garnets have more uvarovite in solution. Clinopyroxene megacrysts show a general decrease in Cr₂O₃ and increase in TiO₂ (0.38–0.56%) with decreasing mg (0.87–0.91). Clinopyroxene megacrysts are more Cr-rich than clinopyroxene in clinopyroxene-ilmenite intergrowths (0.06–0.38% Cr₂O₃) and less Cr-rich than peridotite clinopyroxenes (1.39–1.46% Cr₂O₃). Orthopyroxene megacrysts and orthopyroxene inclusions in olivine megacrysts form two populations: high-Ca, high-Al (1.09–1.16% CaO and 1.16–1.18% Al₂O₃) and low-Ca, low-Al (0.35–0.46% CaO and 0.67–0.74% Al₂O₃). Three orthopyroxenes belonging to a low-Ca subgroup of the high-Ca, high-Al group were also identified (0.86–0.98% CaO and 0.95–1.01% Al₂O₃). The high-Ca, high-Al group (Group I) has lower mg (0.88–0.90) than low-Ca, low-Al group (Group II) with mg=0.92–0.93; low mg orthopyroxenes (Group Ia) have lower Cr₂O₃ and higher TiO₂ than high mg orthopyroxenes (Group II). The orthopyroxene megacrysts have lower Cr₂O₃ than peridotite orthopyroxenes (0.46–0.57% Cr₂O₃). Diopside solvus temperatures indicate equilibration of clinopyroxene megacrysts at 1,165°–1,390° C and 1,295°–1,335° C for clinopyroxene in clinopyroxene-ilmenite intergrowths. P-T estimates for orthopyroxene megacrysts are bimodal: high-Ca, high-Al (Group I) orthopyroxenes equilibrated at 1,165°–1,255° C and 51–53 kb (± 5kb) and the low-Ca, low-Al (Group II) orthopyroxenes equilibrated at 970°–1,020°C and 46–56 kb (± 5kb). Garnet peridotites equilibrated at 1,240°–1,360° C and 47–49 kb. Spinel peridotites have discordant temperatures of 720°–835° C (using spinel-olivine Fe/Mg) and 865°–1,125° C (Al in orthopyroxene).Megacrysts probably precipitated from a fractionating liquid at >150 km depth. They are not disaggregated peridotite because: (1) of large crystal size (up to 1.5 cm), (2) compositions are distinctly different from peridotite phases, and (3) they display fractionation trends. The high mg, low T orthopyroxenes and the clustering of olivine rims near Fo_89–90 reflect liquid changes to higher MgO contents due to (1) assimilation of wall-rock and/or (2) an increase in Fe³⁺/Fe²⁺ and subsequently MgO/FeO as a result of an increase in f _o.     

Equilibration and reaction in Archaean quartz-sapphirine granulite xenoliths from the Lace kimberlite pipe, South Africa

Ultrahigh-temperature quartz-sapphirine granulite xenoliths in the post-Karoo Lace kimberlite, South Africa, comprise mainly quartz, sapphirine, garnet and sillimanite, with rarer orthopyroxene, antiperthite, corundum and zinc-bearing spinel; constant accessories are rutile, graphite and sulphides. Comparison with assemblages in the experimentally determined FMAS and KFMASH grids indicates initial equilibration at >1040 °C and 9–11  kbar. Corona assemblages involving garnet, sillimanite and minor cordierite developed on a near-isobaric cooling P–T  path as both temperature and, to a lesser extent, pressures decreased. Garnet-orthopyroxene Fe-Mg exchange thermometers record temperatures of only 830–916 °C. These estimates do not indicate the peak metamorphic conditions but instead reflect the importance of post-peak Fe-Mg exchange during cooling. Correction of mineral Fe-Mg compositions for this exhange using a convergence approach of Fitzsimons & Harley (1994 ) leads to retrieved P–T  estimates from garnet-orthopyroxene thermobarometry ( c . 1000 °C and 10.5±0.7  kbar) that are consistent with the petrogenetic grid constraints. U-Pb dating of a single zircon grain gives an age of 2590±83  Ma, interpreted as the age of the metamorphic event. Protolith major and trace element chemistries of the xenoliths differ from sapphirine-quartzites typical of the Napier Complex (Antarctica) but are comparable to less siliceous, high Cr and Ni, sapphirine granulites reported from several ultrahigh temperature granulite terranes.     

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.     

Metabasalts from the Mid-Atlantic Ridge: new insights into hydrothermal systems in slow-spreading crust

An extensive suite of hydrothermally altered rocks were recovered byAlvin and dredging along the MARK [Mid-Atlantic Ridge, south of the Kane Fracture Zone (23–24°N)] where detachment faulting has provided a window into the crustal component of hydrothermal systems. Rocks of basaltic composition are altered to two assemblages with these characteristics: (i) type I: albitic plagioclase (An_02–10)+mixed-layer smectite/chlorite or chlorite±actinolite±quartz±sphene, <10% of the clinopyroxene is altered, and there is no trace metal mobility; (ii) type II: plagioclase (An_10–30)+amphibole (actinolite-magnesio-hornblende) +chlorite+sphene, >20% of the clinopyroxene is altered, and Cu and Zn are leached. The geochemical signature of these alteration types reflects the relative proportion and composition of secondary minerals, and the degree of alteration of primary phases, and does not show simple predictive relationships. Element mobilities indicate that both alteration types formed at low water/rock ratios. The MARK assemblages are typical of the greenschist and transition to the amphibolite facies, and represent two distinct, albeit overlapping, temperature regimes: type I-180 to 300°C and type II-250 to 450°C. By analogy with DSDP/ODP Hole 504B and many ophiolites, the MARK metabasalts were altered within the downwelling limb of a hydrothermal cell and type I and II samples formed in the upper and lower portions of the sheeted like complex, respectively. Episodic magmatic and hydrothermal events at slow-spreading ridges suggest that these observed mineral assemblages represent the cumulative effects of more than one hydrothermal event. Groundmass and vein assemblages in the MARK metabasalts indicate either that alteration conditions did not change during successive hydrothermal events or that these assemblages record only the highest temperature event. Lack of retrograde reactions or overprinting of lower temperature assemblages (e.g., zeolites) suggests that there is a continuum in alteration conditions while crustal segments remain in the ridge axis environment. The type II samples may be representative of thereaction zone where compositions of hydrothermal fluids actively venting at the seafloor today become fixed. This prediction necessitates interaction between hydrothermal fluids and intersertal glass and/or mafic phases, in addition to plagioclase, in order to produce the observed range in vented fluid pH.     

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

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

Harzburgite to lherzolite and back again: metasomatic processes in ultramafic xenoliths from the Wesselton kimberlite, Kimberley, South Africa

Garnets from phlogopite harzburgite xenoliths from the Wesselton kimberlite show zoning from low-Ca harzburgitic cores to rims with lherzolitic Ca-Cr relations. Garnet cores are depleted in Y and HREE, but have sinuous REE patterns enriched in the MREE. Rimwards increase in Ca and decrease in Cr and Mg is accompanied by increases in Zr, Y, Ti and HREE. Secondary replacement rims on some garnets consist of garnet with low Ca and Cr, but high Mg, Ti and HREE. The zoning, and the secondary replacement rims, are attributed to different stages of a metasomatic process that has converted harzburgite to lherzolite, at temperatures near 1000 °C. Modelling of zoning profiles suggests that the process can be divided into three parts: (a) Inwards diffusion of Ca, Zr and Y over periods of 10,000–30,000 years, from a fluid depleted in Ti, Ga and Y; (b) formation of overgrowths high in Ca, Zr, Y and Ti, followed by annealing over periods of several thousand years; (c) formation of secondary reaction rims of low-Ca garnet, on very short timescales prior to eruption. The sinuous REE patterns of the garnet cores are regarded as “primary” features reflecting an ancient metasomatic event superimposed on a depleted protolith. The high Zr/Y, Zr/Ti and Zr/Ca of the fluids corresponding to stage (a) are ascribed to the presence of phlogopite and garnet in the matrix near the fluid source (presumed to be a melt, possibly a kimberlite precursor), leading to the development of concentration fronts in the percolating fluid. The overgrowths of stage (b) appear to coincide with the precipitation of phlogopite in the rock. The low Ca of the fluid responsible for the secondary replacement rims of stage (c) may reflect the late precipitation of clinopyroxene or Ca-carbonate as part of the metasomatic assemblage. These processes have significantly modified the modal, major- and trace-element composition of the mantle volume sampled by the Wesselton kimberlite, within <1 Ma of eruption. Recognition of such effects and their distribution in time and space is essential to understanding of the evolution of the subcontinental lithospheric mantle. Received: 11 February 1998 / Accepted: 24 June 1998     

Continuation of the San Andreas fault system into the upper mantle: Evidence from spinel peridotite xenoliths in the Coyote Lake basalt, central California

The Coyote Lake basalt, located near the intersection of the Hayward and Calaveras faults in central California, contains spinel peridotite xenoliths from the mantle beneath the San Andreas fault system. Six upper mantle xenoliths were studied in detail by a combination of petrologic techniques. Temperature estimates, obtained from three two-pyroxene geothermometers and the Al-in-orthopyroxene geothermometer, indicate that the xenoliths equilibrated at 970–1100 °C. A thermal model was used to estimate the corresponding depth of equilibration for these xenoliths, resulting in depths between 38 and 43 km. The lattice preferred orientation of olivine measured in five of the xenolith samples show strong point distributions of olivine crystallographic axes suggesting that fabrics formed under high-temperature conditions. Calculated seismic anisotropy values indicate an average shear wave anisotropy of 6%, higher than the anisotropy calculated from xenoliths from other tectonic environments. Using this value, the anisotropic layer responsible for fault-parallel shear wave splitting in central California is less than 100 km thick. The strong fabric preserved in the xenoliths suggests that a mantle shear zone exists below the Calaveras fault to a depth of at least 40 km, and combining xenolith petrofabrics with shear wave splitting studies helps distinguish between different models for deformation at depth beneath the San Andrea fault system.     

Podiform chromitite in the arc mantle: chromitite xenoliths from the Takashima alkali basalt,Southwest Japan arc

Chromitite xenoliths from the Takashima alkali basalt in the Southwest Japan arc are classified into two types: Type 1 chromitite in thin layers in dunite or wehrlite xenoliths; and Type 2 chromitite in discrete xenoliths which has an orbicular texture, previously documented only from podiform chromitites in ophiolites. Type 1 may be equivalent to layered chromitites in ophiolitic cumulates and Type 2 to podiform chromitites in the transition zone of ophiolites. This example of podiform chromitite from the Southwest Japan arc suggest that these podiform chromitites may exist in the upper mantle beneath an arc, where their formation is favored.     

Contact metamorphism/hydrothermal alteration of Tertiary basalts from the Isle of Skye,northwest Scotland

Alkali olivine basalts from Skye were simultaneously contact metamorphosed by Tertiary gabbro and granite intrusions and altered by the hydrothermal convection system that the plutons induced. Four metamorphic zones were mapped around the plutons. Furthest from the intrusions, in the primary olivine zone, metabasalts are composed of combinations of igneous olivine, augite, plagioclase, titaniferous magnetite, ilmenite, zeolites, gyrolite, sulfides, and chlorite-smectite intergrowths. Closer to the plutons, in the smectite zone, saponite and carbonate appear, primary olivine and gyrolite disappear, and zeolites decrease dramatically in abundance. Still closer to the plutons, in the amphibole zone, actinolite, edenite, chlorite, sphene, epidote, andradite, and quartz appear and saponite and chlorite-smectite intergrowths disappear. Along parts of the contact between gabbro and basalt, in the orthopyroxeneolivine zone, orthopyroxene, metamorphic olivine, and biotite appear and amphibole, chlorite, sphene, epidote, andradite, carbonate, and quartz disappear. Whole-rock chemical data indicate only minor change in the major-element chemical composition of the metabasalts during progressive metamorphism/hydrothermal alteration. Two-pyroxene eothermometry and various mineral-fluid equilibria suggest the range of peak temperatures attained in the metamorphic zones: orthopyroxene-olivine zone, 900°1, 030° C; amphibole zone, 400°–900° C; smectite and primary olivine zones, < 400° C. Mineralogical and oxygen isotopic alteration of the metabasalts were closely coupled: Basalts from the primary olivine zone with nearly unaltered igneous mineralogies have normal or near-normal wholerock ¹⁸O>+5 (SMOW); mineralogically more altered basalts from the smectite zone have whole-rock ¹⁸O=+2 to +5; still more mineralogically altered basalts from the amphibole zone (with one exception) have ¹⁸O<+ 2; completely recrystallized hornfelses from the orthopyroxene-olivine zone have ¹⁸O<0. The principal mechanism of isotope exchange between basalt and metamorphic/ hydrothermal fluid probably was heterogeneous mineralfluid reaction.Metabasalts from the orthopyroxene-olivine zone are mineralogically fresh pyroxene hornfelses that record crystallization temperatures > 1,000° C yet have highly altered whole-rock oxygen isotope compositions, ¹⁸O<0%. The hornfelses chemically interacted with metamorphic/hydrothermal fluids either at very high temperatures or while they were heated to > 1,000° C or both. Their mineralogy, however, rules out significant water-rock interaction after they cooled below 900° C. Hydrothermal convection on Skye was a two-stage process: (a) fluid flow through wall rocks initially was pervasive while they are heated; (b) fluid flow after the thermal peak in the wall rocks was sufficiently channelized that rocks such as those in the orthopyroxeneolivine zone were isolated from further fluid-rock interaction during all or almost all of the cooling history of the hydrothermal system.     

Melting of crustal xenoliths within ascending basalt: Example from the Kula volcanic field,western Anatolia,Turkey

During its storage or ascent, basaltic magma inevitably interacts with the surrounding rocks. In this study, schist xenoliths incorporated within ascending basalt are examined. Heating of the xenoliths combined with decompression effect of rapid magma uprise led to dehydration melting of hydrous minerals producing hercynitic spinel, melt, sillimanite and FeTi oxides. The melt is rhyolitic, strongly peraluminous (1.77 < A/CNK < 2.35) and corundum normative. It may contain up to 8 wt%FeO_t. It occurs between the foliation planes and in the intragranular environment. Dehydration melting of micas in the schist is probably related to combined effects of heating by basaltic magma and decompression due to the rapid rise. Melting of xenoliths was a progressive process at low pressure. To cite this article: H. Bayhan et al., C. R. Geoscience 338 (2006).