Water-saturated melting relations to 5 kilobars of three Leucite Hills lavas

The water-saturated phase relations of three Leucite Hills lavas have been determined at pressures up to 5 kb. Phlogopite is the major primary liquidus phase in orendite and wyomingite at pressures, > 1 kb, but clinopyroxene and olivine are the major primary liquidus phases in madupite at pressures up to 5 kb. Leucite is a liquidus phase in all three magmas at pressures <0.5kb. The experimental results are in reasonable agreement with the inferred crystallization sequences for the Leucite Hills lavas and have applications to the crystallization and differentiation of potassium-rich magmas within the crust.     

Xenoliths in recent basaltic andesite flows from Arenal Volcano,Costa Rica: inference on the composition of the lower crust

Basaltic andesite flows erupted between 1973 and 1980 from Arenal Volcano contain abundant inclusions of anorthosite, olivine gabbro, and pyroxenites, and megacrysts of olivine and anorthite. The anorthosites with large (20 mm) anorthite grains (An_96-92) exhibit deformation twinning and granulation between grain boundaries. Some olivine gabbros have angular clasts of anorthite with bent twins, pyroxene, and olivine in a finer-grained matrix which is distinctly foliated. These textural features suggest that these inclusions were deformed. An exotic (xenolithic) origin is supported in part by the mineral compositions and the estimated temperatures of equilibration: a temperature of about 975° C is obtained by two-pyroxene and Fe-Ti oxide geothermometers for the gabbros, but two-pyroxene temperatures are higher (1064 to 1120° C) for the basaltic andesite host. The olivine gabbro is thought to have crystallized at a pressure between 8.5 and 9.5 kb; whereas the lava phenocrysts crystallized at a much lower pressure of less than 5 kb. These xenoliths probably represent fragments of the lower crust below Arenal volcano. The lava flows show evidence for some contamination especially from fragments of anorthite broken apart from the larger megacrysts and xenoliths. A few phenocrysts of plagioclase in the lava samples have deformation twins. The unusually high Al₂O₃ content (19.4 to 23.2 wt%) of the lava samples can be attributed directly to the addition of anorthite; in fact the observed chemical variation in the lava flows (the increasing alumina and lime contents with decreasing silica) can be explained by this contamination.     

Mafic and silica-rich glasses in mantle xenoliths from Wau-en-Namus,Libya: Textural and geochemical evidence for peridotite–melt reactions

Anhydrous spinel peridotite xenoliths in Quaternary nepheline-basanite and melilite- or sodalite-bearing lavas of the Wau-en-Namus volcano in S Libya range from lherzolites to harzburgites recording melt extraction in a shallow setting (≤ 2 GPa). Primary clinopyroxenes have distinct trace element characteristics documenting LILE (large ion lithophile element) depletion or enrichment events predating the formation of glass pockets and veins in the xenoliths. These glasses are aluminous and alkali-rich, range in composition from ultrabasic to silicic (43–67 wt.% SiO₂) and may contain empty vugs and micro-phenocrysts of olivine, clinopyroxene, spinel, plagioclase, sodalite, apatite that are similar in composition to phenocrysts in the host lavas. Reactions of infiltrating melt and xenolith minerals are documented by diffuse Fe–Ca-rich rims of olivine in contact with glass, and by spongy-textured reaction domains caused by incongruent dissolution of primary pyroxenes and spinel. Some glasses have trace element characteristics similar to that of the host Ne-basanite, suggesting they were derived from the same source during entrainment and transport to the surface. Incompatible element enrichment and Sr–Nd isotopic compositions of the analyzed host lava are similar to HIMU (high μ; μ = ²³⁸Pb/²⁰⁴Pb)-type magmas, but the Pb isotopic composition is less radiogenic compared to other intra-plate Neogene magmatic rocks from N Africa.     

Mantle-derived lherzolite xenoliths and megacrysts from Permo-Triassic dykes,Sunnhordland, western Norway

Permo-Triassic alkaline dykes in the Sunnhordland region contain angular inclusions of spinellherzolite composed of olivine (Fo_89.5), high-alumina pyroxenes, and Al₂O₃-rich spinel. Mineral chemistry suggests that the lherzolites represent mantle material which equilibrated at temperatures in the ranges 1050 to 1150°C, compatible with an oceanic geotherm. Megacrysts of augite and spinel are associated with the xenoliths, and have compositions which differ from analogous phases occurring both as phenocrysts and as xenolith constituents. Systematic chemical variations in the clinopyroxene megacrysts may reflect magmatic fractionation processes. Megacrysts may represent disaggregated parts of coarsely crystalline polymineralic assemblages precipitated at high pressures, and temperatures above that indicated by the xenoliths, with subsequent exsolution at temperatures of about 1060°C.     

Ferric-ferrous ratios,H2O contents and D/H ratios of phlogopite and biotite from lavas of different tectonic regimes

 Complete chemical analyses, including ferric and ferrous iron, H₂O contents and δD values for 16 phlogopite and biotite and 2 hornblende separates are presented. Samples were obtained from volcanic rocks from four localities: (1) phlogopite phenocrysts from minette lavas from the western Mexico continental arc, (2) biotite and hornblende phenocrysts from andesite lavas from Mono Basin, California, (3) phlogopite and biotite from clinopyroxenite nodules entrained in potassic lavas from the East African Rift, Uganda, and (4) phlogopite phenocrysts from a wyomingite lava in the Leucite Hills, Wyoming. The Fe₂O₃ contents in the micas range from 0.8 to 10.5 wt%, corresponding to 0.09 to 1.15 Fe³⁺ per formula unit (pfu). Water contents vary from 1.6 to 3.0 wt%, corresponding to 1.58 to 3.04 OH pfu, significantly less than would be expected for a site fully occupied by hydroxyl. Cation- and anion-based normalization procedures provide accurate mineral formulae with respect to most cations and anions, but are unable to generate accurate estimates of Fe³⁺/Fe^T, and overestimate OH at the expense of O on the hydroxyl site. These inaccuracies are present despite acceptable adjusted totals and stoichiometric calculated site occupancies. The phlogopite and biotite phenocrysts in arc-related lavas from western Mexico and eastern California have the highest Fe³⁺/Fe^T ratios (56–87%), reflecting high magmatic oxygen fugacities (ΔNNO = +2 to +5), in contrast to those from Uganda (25–40%) and the Leucite Hills (23%). There is no correlation between the OH content and the Fe³⁺/Fe^T ratio in the micas. Values of KMg/Fe²⁺D (± 2σ errors) were calculated for three phlogopite-olivine pairs (0.12 ± 0.12, 0.26 ± 0.14, 0.09 ± 0.12), two biotite-hornblende pairs (0.73 ± 0.08 and 1.22 ± 0.10) and a single phlogopite-augite pair (1.15 ± 0.12). Values of KF/OHD for two biotite and hornblende pairs could not be determined without significant error because of the extremely low F contents (< 0.2 wt%) of the four phases. The δD values obtained in this study encompass a large range (−137 to −43‰). The phlogopite and biotite separates from Uganda have δD values of −70 to −49‰, which overlap those believed to represent “primary” mantle. There is a larger range in δD values (−137 to −43‰) for phlogopite phenocrysts from western Mexico minette lavas, although their range in δ¹⁸O values (5.2–6.2‰) is consistent with “normal” mantle. It is unlikely, therefore, that the variable δD values reflect heterogeneity in the mantle source region of the minette magmas. Nor can the extremely low δD values reflect degassing of H₂ or H₂O since almost 100% loss of dissolved water in the magma is required, an unrealistic scenario given the stability of the hydrous phenocrysts. The very low δD values of the Mascota minette phlogopites require that the hydrogen be introduced from an external source (e.g., meteoric water). Whatever the process responsible for the observed hydrogen isotope composition, it had no effect on the δ¹⁸O value, f _{O 2}, a _{H 2O} or bulk composition of the host magmas. Received: 5 January 1995 / Accepted: 19 March 1996     

Petrology and geochemistry of Rodrigues Island,Indian Ocean

Rodrigues Island is composed of a differentiated series of transitional-mildly alkaline olivine basalts. The lavas contain phenocrysts of olivine (Fo_88–68)±plagioclase (An_73–50), together with a megacryst suite involving olivine, plagioclase, kaersutite, clinopyroxene, apatite, magnetite and hercynite-rich spinels. Troctolitic-anorthositic gabbro xenoliths are widely dispersed throughout the lavas and are probably derived from the upper parts of an underlying layered complex: the megacrysts may originate from coarse, easily disaggregated differentiates near the top of this body.Modelling of major and trace element data suggests that the majority of chemical variation in the lavas results from up to 45% fractionation of olivine, clinopyroxene, plagioclase and magnetite at low pressures, in the ratio 2035396. The clinopyroxene-rich nature of this extract assemblage is significantly different to that of the xenoliths, and suggests that clinopyroxene-rich gabbros and/or ultrabasic rocks may lie at greater depth.Sr and Nd isotopic data (⁸⁷Sr/⁸⁶Sr 0.70357–070406,¹⁴³Nd/¹⁴⁴Nd 0.51283–0.51289) indicate a mantle source with relative LREE depletion, and emphasise an unusual degree of uniformity in Indian Ocean island sources. A small group of lavas with strong HREE enrichment suggest a garnet-poor source for these, while high overall Al₂O₃/ CaO ratios imply high clinopyroxene/garnet ratios in refractory residua.     

Primary basalts and magma genesis

A representative Quaternary clinopyroxene leucitite lava from the Alban Hills, Roman comagmatic province, central Italy, has been subjected to anhydrous thermal experiments within its melting range at pressures up to 45 kb. The lava contains 2.2% of leucite and 1.4% of diopside phenocrysts in a fine-grained groundmass, suggesting that these phases were crystallizing on the liquidus of the magma immediately prior to its eruption. This situation is reproduced experimentally at 14 kb and 1260 °C. As there is no evidence that the H₂O content of this lava was appreciable, it is concluded that the anhydrous experimental results give a valid indication that this leucitite equilibrated with its phenocrysts at approximately 50 km depth, about 25 km into the upper mantle, before final rapid uprise. Comparison of the bulk compositions of Alban Hills mafic leucitites with that of the eutectic in the synthetic system Diopside-Leucite as a function of pressure confirms the conclusion of the high-pressure experiments. In contrast, the dilc ratios of other Roman province mafic leucitites indicate that they equilibrated within the upper crust prior to eruption. Published Sr and O-isotope studies show unequivocally that, when the Alban Hills mafic leucitites and their phenocrysts equilibrated, the magmas contained a substantial fraction of melt from crustal rocks. These data are reconciled with the experimental demonstration that the magmas evolved entirely within the upper mantle by postulating that their crustal components were derived from partial fusion of Tyrrhenian ocean-floor sediments, subducted beneath Italy during the anticlockwise rotation of the Corsica-Sardinia lithospheric microplate. The Roman province volcanics show considerable chemical similarities with lavas from converging plate margins elsewhere, together with substantial differences from other occurrences of strongly-potassic rocks. It is concluded that this magma type may be polygenetic.     

The mineralogy and petrology of the volcanic rocks from the Leucite Hills,Wyoming

Examples of the three volcanic rock types, wyomingite, orendite and madupite from the Leucite Hills have been examined with the electron microprobe. The results show that leucite is non-stoichiometric as predicted byCross (1897), having an excess of potassium and silicon, and that the only feldspar found, a sanidine, contains up to 18 percent of the iron-feldspar molecule. The co-existing phlogopite, diopside and olivine together with the groundmass amphibole are all highly magnesian. Of the varied accessory minerals, priderite (K₂Ti₈O₁₆) and wadeite (K₄Zr₂Si₆O₁₈) have been identified and analyzed together with ubiquitous apatite and perovskite, both of which contain rare earths in abundance. Comparative mineralogical data has been obtained on a few representative specimens from West Australia and on the jumillite from Spain.The new rock analyses together with the existing data from the Leucite Hills show the rare but characteristic molecular excess of potassium over aluminium; this excess is considered to account for the ahsence of the iron-titanium oxides in the orendites and wyomingites, and of course for the unusual composition and species of the minerals. Exploratory melting experiments show that these potassic lavas have a comparable melting range to magnesian basalts, and a crustal origin is thereby considered precluded. There is no evidence that sialic contamination contributed notably to the composition of the oversaturated orendites and wyomingites, and their relationship by any process of crystal fractionation to the undersaturated madupite is obscure. The generation of madupite could be achieved by crystal fractionation at high pressure of a liquid derived by partial fusion of mantle material.     

Crystallization temperature of wyomingite from Leucite Hills

Wyomingite collected from Leucite Hills is composed mainly of leucite, diopside, phlogopite, and small amounts of apatite, calcite, magnetite and rare amphibole, and is characterized by very high content of potash. Thermal experiments at atmospheric pressure indicate that the liquidus phase is always diopside with liquidus temperature of 1320 °C, and solidus temperature is about 1000 °C. Various kinds of melt inclusions are abundant in all constituent minerals. They comprise mono-phase (glass only), two-phase (gas+glass), three-phase (gas+glass+one crystalline phase) and multi-phase (gas+glass+more than two crystalline phases) inclusions. Thermal experiments have been made on these inclusions in phlogopite, diopside, and leucite in order to estimate the temperature of crystallization by homogenizing these inclusions. The results show that the crystallization of wyomingite began with formation of phlogopite accompanied by diopside at 1270 °C. Although diopside ceased crystallization at 1220 °C recurrent crystallization of phlogopite was noticed between 1120 ° and 1040 °C. Leucite crystallized out abundantly between 1250 ° and 1150 °C. Complete solidification of wyomingite occurred at about 1000 °C.     

Nd and Sr isotopes in ultrapotassic volcanic rocks from the Leucite Hills,Wyoming

Nd and Sr isotopic compositions and Rb, Sr, Sm and Nd concentrations are reported for madupites, wyomingites and orendites from the Pleistocene volcanic field of the Leucite Hills, Wyoming. All Leucite Hills rocks have negative εNd signatures, indicating derivation or contribution from an old light rare earth element (LREE) enriched source. In this respect they are similar to all occurrences of high potassium magmas so far investigated. But Sr isotopic variations are comparatively small and ⁸⁷Sr/ ⁸⁶Sr ratios are unusually low for high-K magmas (0.7053–0.7061, one sample excluded). These values suggest that the light REE enrichment of the source was not accompanied by a strong increase in Rb/Sr. Wyomingites and orendites are isotopically indistinguishable which is consistent with chemical and petrographic evidence for their derivation from a common magma series depending on emplacement conditions. Basic to ultrabasic madupites and more silicic wyomingites/orendites are distinct in their Nd isotopic variations (madupites: εNd= ?10.5 to ?12.3; wyomingites/orendites: εNd= ?13.7 to ?17.0) despite similar Sm/Nd ratios and complete overlap in ⁸⁷Sr/⁸⁶Sr. Selective or bulk assimilation of crustal material is unlikely to have significantly affected the Nd and Sr isotopic compositions of the magmas. The measured isotopic ratios are considered to reflect source values. The distinct isotopic characteristics of madupite and wyomingite/orendite magmas preclude their derivation by fractional crystallization, from a common primary magma, by liquid immiscibility or by partial melting of a homogeneous source. Two isotopically distinct, LREE enriched and slightly heterogeneous sources are required. Heterogeneities were most pronounced between magma sources from each volcanic centre (butte or mesa). The relationship between the madupite and wyomingite/orendite sources and their evolution is discussed on the basis of two simple alternative sets of models:

1. a two-stage evolution model with an old enrichment event (a metasomatic event?) perhaps taking place during the stabilization of the Wyoming Craton 3.2 to 2.5 Gyr ago but not later than 1.2 Gyr ago or
2. a mixing model involving mixing between one endmember with εNd near zero and another end-member with a strong negative εNd signature.

     

Petrological and experimental evidence for differentiation of water-rich magmas beneath St. Kitts,Lesser Antilles

St. Kitts lies in the northern Lesser Antilles, a subduction-related intraoceanic volcanic arc known for its magmatic diversity and unusually abundant cognate xenoliths. We combine the geochemistry of xenoliths, melt inclusions and lavas with high pressure–temperature experiments to explore magma differentiation processes beneath St. Kitts. Lavas range from basalt to rhyolite, with predominant andesites and basaltic andesites. Xenoliths, dominated by calcic plagioclase and amphibole, typically in reaction relationship with pyroxenes and olivine, can be divided into plutonic and cumulate varieties based on mineral textures and compositions. Cumulate varieties, formed primarily by the accumulation of liquidus phases, comprise ensembles that represent instantaneous solid compositions from one or more magma batches; plutonic varieties have mineralogy and textures consistent with protracted solidification of magmatic mush. Mineral chemistry in lavas and xenoliths is subtly different. For example, plagioclase with unusually high anorthite content (An_≤100) occurs in some plutonic xenoliths, whereas the most calcic plagioclase in cumulate xenoliths and lavas are An₉₇ and An₉₅, respectively. Fluid-saturated, equilibrium crystallisation experiments were performed on a St. Kitts basaltic andesite, with three different fluid compositions (XH₂O = 1.0, 0.66 and 0.33) at 2.4 kbar, 950–1025 °C, and fO₂ = NNO ? 0.6 to NNO + 1.2 log units. Experiments reproduce lava liquid lines of descent and many xenolith assemblages, but fail to match xenolith and lava phenocryst mineral compositions, notably the very An-rich plagioclase. The strong positive correlation between experimentally determined plagioclase-melt Kd_Ca–Na and dissolved H₂O in the melt, together with the occurrence of Al-rich mafic lavas, suggests that parental magmas were water-rich (> 9 wt% H₂O) basaltic andesites that crystallised over a wide pressure range (1.5–6 kbar). Comparison of experimental and natural (lava, xenolith) mafic mineral composition reveals that whereas olivine in lavas is predominantly primocrysts precipitated at low-pressure, pyroxenes and spinel are predominantly xenocrysts formed by disaggregation of plutonic mushes. Overall, St. Kitts xenoliths and lavas testify to mid-crustal differentiation of low-MgO basalt and basaltic andesite magmas within a trans-crustal, magmatic mush system. Lower crustal ultramafic cumulates that relate parental low-MgO basalts to primary, mantle -derived melts are absent on St. Kitts.     

Igneous scapolite-bearing associations in the Chaîne des Puys,Massif Central (France) and Atakor (Hoggar,Algeria)

A scapolite+amphibole+clinopyroxene+Fe-Ti oxide+apatite association has been found as megacrysts in tephra from the Enval-Volvic volcanic line, east of the Chaîne des Puys (Massif Central, France) and in the cinder cone of the Segueïka volcano (Atakor, Algeria). In both kinds, lavahosts are basanites. Although never seen together in a single xenolith, a study of their inclusions indicates close genetic relationship between all 5 phases. This association must be considered as a paragenesis that crystallized within a narrow PT range. Volcanological, petrological and geochemical data suggest that these megacrysts are high-pressure phenocrysts rather than mechanically desintegrated fragments derived from coarse rocks. The composition of the amphibole suggests a pressure between 5 and 15 kb; Fe-Ti oxides imply a temperature close to 1,100° C.Crystallization of sulfur-rich scapolite involves a high fSO₃, and therefore a high fO₂, remarkable for such relatively undifferenciated alkalic magmas. Coexisting Fe-Ti oxides indicate a fO₂ close to 10^–6 bar. Such conditions imply that H₂O was a major component of the gaseous phase. This high water content can be explained in terms of derivation from an hydrated upper mantle source. This is in agreement with other petrological evidences indicating that the basic magmas of the Massif Central crystallized under high fSO₃ conditions.     

Characteristics of the lithospheric mantle beneath East Serbia inferred from ultramafic xenoliths in Palaeogene basanites

Mantle xenoliths from Paleogene basanites of East Serbia were studied using EMP and LA-ICP-MS techniques in order to better understand mantle characteristics in this region. Five different mantle lithologies have been distinguished: a dunite/harzburgite/lherzolite (D/HZ/L) group, clinopyroxene-rich lherzolites (Cpx-L), clinopyroxene megacrysts (Cpx-M), spinel-rich olivine websterites (OWB₁) and spinel-poor olivine websterites (OWB₂). D/HZ/L xenoliths are the most common and represent normal mantle composed of typical anhydrous spinel peridotites with well equilibrated, unzoned silicates characterized by high Mg# s. Negative correlations between Mg# and TiO₂, Al₂O₃ and CaO wt% in clinopyroxenes (cpx) and orthopyroxenes (opx) and the Cr–Al trend in spinel (sp) suggest depletion via extraction of basaltic melts. The modal composition of D/HZ/L xenoliths and unusual low-Al opx suggest that the lithospheric mantle underneath East Serbia is more depleted than normal European lithosphere. D/HZ/L xenoliths contain numerous pockets and veins filled by Cr-rich cpx, Ti-rich spinel, altered glass, apatite and rare ilmenite and phlogopite. Petrographic observations, supported by major element contents in sp and cpx, and modelling using trace element contents in cpx, indicate that the pockets and veins formed from infiltration of alkaline melts and reaction with peridotite wall-rock causing opx and spinel replacement. The same alkaline melt-related metasomatism gave rise to the Cpx-L and OWB₁ mantle xenoliths and Cpx-M xenocrysts. Trace element contents of cpx in these xenoliths show a distinctively concave downwards REE pattern with a HFSE depletion, very similar to cpx megacrysts from the Pannonian Basin and to vein cpx from Eifel. In contrast, the OWB₂ xenoliths show evidence of precipitation from subduction-related mafic to ultramafic melts, as inferred from their opx-rich lithology and unusual Cr-rich spinels. They are probably related to subduction magmatism during the Late Cretaceous.Milivoje Jovanovi: deceased in April 2004     

Primary alkaline magmas associated with the Quaternary Alligator Lake volcanic complex,Yukon Territory,Canada

The Alligator Lake complex is a Quaternary alkaline volcanic center located in the southern Yukon Territory of Canada. It comprises two cinder cones which cap a shield consisting of five distinct lava units of basaltic composition. Units 2 and 3 of this shield are primitive olivine-phyric lavas (13.5–19.5 cation % Mg) which host abundant spinel lherzolite xenoliths, megacrysts, and granitoid fragments. Although the two lava types have erupted coevally from adjacent vents and are petrographically similar, they are chemically distinct. Unit 2 lavas have considerably higher abundances of LREE, LILE, and Fe, but lower HREE, Y, Ca, Si, and Al relative to unit 3 lavas. The ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd isotopic ratios of these two units are, however, indistinguishable. The differences between these two lava types cannot be explained in terms of low pressure olivine fractionation, and the low concentrations of Sr, Nb, P, and Ti in the granitoid xenoliths relative to the primitive lavas discounts differential crustal contamination. The abundance of spinel lherzolite xenoliths and the high Mg contents in the lavas of both units indicates that their compositional differences originated in the upper mantle. The Al and Si systematics of these lavas suggests that, compared to unit 3 magmas, the unit 2 magmas may have segregated at greater depths from a garnet lherzolite mantle. The identical isotopic composition and similar ratios of highly incompatible elements in these two lava units argues against their differences being a consequence of random metasomatism or mantle heterogeneity. The lower Y and HREE contents but higher concentrations of incompatible elements in the unit 2 lavas relative to unit 3 can be most simply explained by differential partial melting of similar garnet-bearing sources. The unit 2 magmas thus appear to have been generated by smaller degrees of melting at a greater depth than the unit 3 magmas. The contemporaneous eruption of two distinct but volumetrically restricted primary magmas from adjacent vents at the Alligator Lake volcanic complex suggests that volcanism in this region of the Canadian Cordillera is controlled by localized, small batch processes.     

Petrological and geochemical relationships between pyroxene megacrysts and associated alkali-basalts from Massif Central (France)

Major, trace element, and REE analyses, as well as Sr isotopic ratios, have been obtained on twelve clinopyene megacrysts and phenocrysts and their alkali-basalt hosts from the French Massif Central. Equilibrium between crystals and host was examined based on petrographic and geochemical data.Two types of pyroxenes are recognized: the acmite-bearing clinopyroxenes, rich in incompatible elements and the salitic clinopyroxenes, poor in incompatible elements. ⁸⁷Sr/ ⁸⁶Sr isotopic data reveal no significant difference between clinopyroxenes and host lavas: they are in apparent isotopic equilibrium. The Sr isotopic ratios of the two types of pyroxenes are also quite similar. However pyroxene crystals from the first group are not in equilibrium with their host; they have crystallized at high-pressure from differentiated alkali-lavas and have been incorporated in a more primitive magma. Pyroxene crystals from the second group are in apparent equilibrium with their host lava; they have crystallized at various pressures. For the latter, distribution coefficients are proposed for compatible elements, trace elements and REE.     

Exsolved garnet-bearing pyroxene megacrysts from some South African kimberlites

Clinopyroxene and orthopyroxene megacrysts containing garnet lamellae up to 1.2 mm thick as an exsolved phase are found rarely in kimberlites from Frank Smith and Bellsbank. Chemically the clinopyroxenes are characteristically subcalcic, being within the range of 100 Ca/Ca + Mg + Fe = 27 to 36, and the orthopyroxenes are characterized by high Al₂O₃ and Cr₂O₃. Immediately after crystallization during very slow cooling, clinopyroxene and orthopyroxene exsolve wide-spaced orthopyroxene and clinopyroxene phases parallel to (100) of the host phases, respectively, then both host and exsolved phases exsolve garnet lamellae. Topotactic relations between pyroxenes and garnet are determined by X-ray for the first time. Partitioning of major and minor elements among the coexisting clinopyroxene, orthopyroxene and garnet in pyroxene megacrysts is the same as that of the granular-type garnet peridotite xenoliths in Lesotho and South African kimberlies. Mineralogy and chemistry indicate that subcalcic clinopyroxene and orthopyroxene megacrysts contain respectively about 10 and 3 mole % of the garnet molecule in solid solution.     

Stages in the P-T path of ascending basalt magma: An example from San Quintin,Baja California

Late Pleistocene or Recent lavas from San Quintin, Baja California are basanitoids and alkali basalts. The surface quench temperatures of the lavas average 1 005° C with log =–11.4, as deduced from the groundmass Fe-Ti oxides. Spinel lherzolite xenoliths and megacrysts of augite and andesine have been found in lava flows and cinder deposits. Using analytical data on the rocks and minerals and simple thermodynamic expressions, the pressures and temperatures of equilibration of lavas and xenoliths, megacrysts and phenocrysts have been calculated. The lavas could have been in equilibrium with lherzolite at 1 330–1 410° C and 27.5–31.6 kb, the more silica-poor liquid having the higher values. The basanitoid could have equilibrated with the megacrysts at about 10.5 kb and with phenocrysts at about 1.4 kb and 1130° C. The variation in composition of the lavas may be explained by a rising zone of melting within the mantle, the most silica-poor liquid having the deepest source. The source of the San Quintin basalts is probably related to spreading of the ocean floor in the Gulf of California.     

Multiple origins of clinopyroxenes in alkali basaltic rocks

Geochemical and textural data on clinopyroxenes in individual alkali basaltic flows from provinces in eastern Australia and the Massif Central can be used to differentiate four different modes of origin (three at high pressure) for these clinopyroxenes. Many single flows from the two provinces contain clinopyroxenes of three, or even four, of these origins. Rare flows contain core clinopyroxene with overgrowths of clinopyroxenes of two distinct generation. Each of the overgrowth is compositionally analogous to clinopyroxenes occurring in xenoliths or as discrete crystals in the same host lava. Such rimming relationships provide evidence that the host magma has undergone high pressure crystallisation and confirm that some xenoliths and megacrysts are cognate. With decreasing pressure the major changes in clinopyroxene chemistry are an increase in the ratio Al^lv/Al^vi, a linear increase of atomic proportions of Ti and Al with decreasing Si, and an increase in the Ti: (100 Mg/(Mg + Σ Fe)) ratio of the pyroxenes. Al₂O₂ wt, % is an unreliable potential geobarometric indicator; consideration of tetrahedral and octahedral site occupancies by Al (Al^lv/Al^vl ratio) is necessary. High-pressure fractionation dominated by clinopyroxene is postulated for some basaltic-composition, resulting in SiO₂ depletion, alkali enrichment and decrease in the Mg/(Mg + Fe²⁺) value of the host magma.     

Petrology of Anorthite-bearing Gabbroic Anorthosite Dykes in northwest Skye

A group of gabbroic anorthosite dykes in northwest Skye containsmegacrysts of calcic plagioclase (An_93–87) and olivine(FO_87–78.5and plagioclase-rich xenoliths set in a matrixof low-alkali, high Ca olivine tholeiite. Field, mineralogicand petrochemical evidence indicates (1) that the dykes arefilled with crystals concentrated from magmas feeding lava flowsand (2) that, although the megacrysts crystallized from low-alkali,high Ca olivine tholeiite magmas at depths <4 km, the megacrystsand the matrix in each dyke are not cognate. The emplacementtemperature was less than 1230 °C. Low-alkali, high Ca olivinetholeiite is an abundant Hebridean magma type, resembling unfractionatedoceanic tholeiites from the Atlantic. The temporal change fromalkali olivine basalt to low-alkali, high Ca olivine tholeiitein the Hebridean proto-spreading centre may mimic compositionalchanges during initial development of the mid-Atlantic ridge.     

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.