On the origin of some mica-lamprophyres: experimental evidence from a mafic minette

Experimental melting relationships for a mafic minette (mica-lamprophyre) from Buell Park, Arizona were determined under fO₂ conditions equivalent to the ironwüstite-graphite and quartz-fayalite-magnetite buffers, at pressures of 10–20 kbar. A comparison between experimental products and phenocrysts in the most primitive minettes indicates that those lavas preserve a near-liquidus assemblage of olivine, diopside and Ti-rich phlogopite crystallized in the upper mantle under fO₂QFM and in the presence of an H₂O-bearing fluid phase. It is suggested that micalamprophyric (minette) magmas may originate from a metasomatized, garnet-bearing peridotitic source at deeper levels in the mantle (P20 kbar) but can also be in equilibrium with a phlogopite-bearing wehrlite (±opx) source at pressures of 17–20 kbar, under reducing or oxidizing mantle conditions. Owing to their rapid crystallization rate and high liquidus temperatures, a series of potassic daughter melts (potassic latites and felsic minettes) can be formed by segregation from mafic minette parents during their ascent through the cooler continental crust. The preservation of olivine in equilibrium with phlogopite phenocrysts in primitive minettes precludes a petrogenetic process dominated by assimilation/fractional crystallization in a shallow magma chamber and supports a model by which some lamprophyric magmas are brought to near surface conditions at temperatures in the range of 1,000–1,200° C and chilled rapidly.     

Potassic Mafic Lavas of the Bearpaw Mountains, Montana: Mineralogy, Chemistry, and Origin

The volcanic rocks of the Bearpaw Mountains are part of theMontana high-potassium province, emplaced through Archaean rocksof the Wyoming Craton between 54 and 50 Ma ago. Extrusive rocks,dominated by minettes and latites, have a volume of 825 km³.The minettes range in composition from 20 to 6% MgO. The moremagnesian varieties contain the phenocryst assemblage forsterite+ Cr-spinel + diopside phlogopite. More evolved rocks areolivine-free, with an assemblage of either salite + phlogopite+ pseudoleucite or salite + phlogopite + analcime. The analcimeis thought to be secondary after leucite, produced by loss ofpotassium from the minettes. Mineral chemistry and textures,especially of clinopyroxenes, indicate that mixing between minettemagmas of varying degrees of evolution was commonplace. Compositionalvariation was further extended by accumulation of olivine +spinel + clinopyroxene phenocrysts, and by the preservationof mantle xenocrysts in the minettes. The primary minette magmasare inferred to have had 12–14% MgO and to have been generatedat 30 kb from an olivine + diopside + phlogopite-bearing source.The primary magmas evolved dominantly by fractionation of olivine+ diopside. The minettes have high contents of large ion lithophile elements(LILE) and light rare earth elements (LREE), with K₂O up to6.18%, Ba 5491 ppm, Sr 2291 ppm, and Ce 99 ppm. (⁸⁷Sr/⁸⁶Sr)⁰ranges from 0.707 to 0.710 and Nd varies from –10 to–16. These data, plus high LILE/HFSE (high field strengthelements) values, are interpreted to show that the minettescontain at least three different mantle components. The lithospherewas initially depleted in Archaean times, but was metasomaticallyenriched in the Proterozoic and in the late Cretaceous and earlyTertiary. The latites have many chemical features in common with the minettes,such as potassic character and high LILE/HFSE values. They formedby fractional crystallization of minette magma in combinationwith assimilation of crustal rocks; this process enriched themagmas in SiO₂ and raised Na₂O/K₂O and ⁸⁷Sr/⁸⁶Sr values. Chemicaldata for phenocrysts and bulk rocks in minettes suggest mixingbetween minette and latite magmas.     

Alkaline and calc-alkaline lavas near Los Volcanes,Jalisco, Mexico: geochemical diversity and its significance in volcanic arcs

A remarkably diverse suite of lavas erupted during the late-Pliocene at the volcanic front of the western Mexican Volcanic Belt near the town of Los Volcanes, Jalisco. This region is much closer to the Middle America Trench than the main axis of Quaternary andesite-dacite stratovolcanoes, and volcanism occurred in a complex tectonic regime involving both subduction of the young Rivera Plate and transverse crustal extension of the Jalisco structural block. The variety of lava types covers a wide spectrum from highly potassic minettes and leucitites to calc-alkaline basalts and andesites which are compositionally similar to those erupted elsewhere in the Mexican Volcanic Belt. Other alkaline varieties intermediate between these extremes include absarokites, trachybasalts and trachyandesites. Phlogopite, amphibole and apatite are common phenocryst phases; whole-rock compositions show a wide range of alkali contents (e.g. K₂O of 1.0–8.6 wt.%), and typically contain >5 wt.% MgO. MgO, Ni, V and Cr show little systematic decrease with increasing SiO₂, suggesting that these lavas have evolved from primitive, mantle derived magmas with a wide range of SiO₂ contents. Strong enrichments in incompatible trace elements are observed in all of the lavas (Sr 700–5100 ppm, Ba 470–4800, Ce 22–325 ppm, Zr 90–700 ppm), as is the relative enrichment of large ion lithophile (Ba, Sr, Rb) and light rare-earth elements (La, Ce) over the high field strength elements (Ti, Zr) which is typical of magmas in volcanic arcs. This enrichment pattern suggests that these magmas come from source regions which contain incompatible element-rich phases such as phlogopite, amphibole and apatite. The petrological and geochemical features of the lavas which occur in the Los Volcanes region provide direct evidence of the extreme heterogeneity which may exist in magma source regions at convergent margins. The complex tectonic regime in western Mexico further suggests that rifting and crustal extension play an important role in the generation and successful ascent of melts from enriched regions of the sub-arc mantle.     

Origin of coexisting minette and ultramafic breccia,Navajo volcanic field

Trace element evidence indicates that at the Buell Park diatreme, Navajo volcanic field, the felsic minette can be best explained by crystal fractionation from a potassic magma similar in composition to the mafic minettes. Compatible trace element (Cr, Ni, Sc) abundances decrease while concentrations of most incompatible elements (Ce, Yb, Rb, Ba, Sr) remain constant or increase from mafic to felsic minette. In particular, the nearly constant Ce/Yb ratio of the minettes combined with the decrease in Cr, Ni, and Sc abundances from mafic to felsic minette is inconsistent with a model of varying amounts of partial melting as the process to explain minette compositions. The uniformity of rare earth element (REE) abundances in all the minettes requires that an accessory mineral, apatite, dominated the geochemistry of the REE during fractionation. A decrease in P₂O₅ from mafic to felsic minette and the presence of apatite in cognate inclusions are also consistent with apatite fractionation. Higher initial⁸⁷Sr/⁸⁶Sr ratios in the felsic minettes relative to the proposed parental mafic minettes, however, is inconsistent with a simple fractionation model. Also, a separated phlogopite has a higher initial⁸⁷Sr/⁸⁶Sr ratio than host minette. These anomalous isotopic features probably reflect interaction of minette magma with crust.The associated ultramafic breccia at Buell Park is one of the Navajo kimberlites, but REE concentrations of the matrix do not support the kimberlite classification. Although the matrix of the breccia is enriched in the light REE relative to chondrites, and has high La, Rb, Ba, and Sr concentrations relative to peridotites, the concentrations of these elements are significantly lower than in South African kimberlites. A high initial⁸⁷Sr/⁸⁶Sr ratio combined with petrographic evidence of ubiquitous crustal xenoliths in the Navajo kimberlites suggests that the relatively high incompatible element concentrations are due to a crustal component. Apparently, Navajo kimberlites are most likely a mixture of comminuted mantle wall rock and crustal material; there is no evidence for an incompatible element-rich magma which is characteristic of South African kimberlites.If the mafic minettes are primary magmas derived from a garnet peridotite source with chondritic REE abundances, then REE geochemistry requires very small (less than 1%) degrees of melting to explain the minettes. Alternatively, the minettes could have formed by a larger degree of melting of a metasomatized, relatively light REE-enriched garnet peridotite. The important role of phlogopite and apatite in the differentiation of the minettes supports this latter hypothesis.     

The Colima volcanic complex,Mexico: Part II. Late-quaternary cinder cones

Since the late Pleistocene, eleven cinder and lava cones have erupted on the floor of the southern Colima graben, NE and NW of the large, active, andesitic volcano Colima. Scoria and lava samples from nine of the cones form a completely transitional basic alkalic series including basanites (9), leucite-basanites (3), and minettes (15), the commonest variety of mica lamprophyre. These samples represent primitive, high temperature magmas with 47.6–50.3% SiO₂, 7.4–15.3% MgO, 2.5–4.4% K₂O, and 2.2–9.9% normative nepheline. All members of this basic alkalic suite contain Mg-olivine (Fo_75–94), chromite, augite, and late plagioclase and titanomagnetite. The petrographic transition from basanite to minette is marked by the appearance of sanidine and the volatile-bearing phases phlogopite, apatite, and analcime during late stages of crystallization. As these phases increase in abundance, presumably reflecting a rise in magmatic volatile content, there are corresponding increases in the whole rock concentrations of 16 incompatible elements. Although these incompatible elements are relatively abundant even in the basanites, many are highly concentrated in the minettes: Ba 4,200 ppm, Sr3,100 ppm, Zr 550 ppm, Ce190 ppm, Hf 18 ppm. Among the incompatible elements, the degrees of enrichment in the minettes relative to the basanites decrease in the order: H, Th, Ce, La, Nd, Zr, Hf, U, Ba, Sm, Eu, Pb, P, Nb, Sr, Ti. These enrichments may reflect the increasing importance of minor, incompatible element rich mantle phases during partial melting. The concentrations of alkali metals K, Na, Rb, and Cs do not correlate with these other elemental enrichments. The leucite-basanties have similar incompatible element contents to many minettes, differing from them only in the presence of leucite rather than analcime, and Ti-F-rich groundmass phlogopite rather than hydrous phlogopite phenocrysts; thus the leucite-basanites represent relatively dry equivalents of minettes.Two of the eleven cinder cones are calc-alkaline in nature and do not belong to the basanite-minette group; the easternmost cone is constructed of high-Al basalt, and the northernmost of basaltic andesite. The high-Al basalt (49.5% SiO₂, 9.3% MgO, 221 ppm Ni) closely approximates a parental magma to the post-caldera andesitic suite of V. Colima (56.5–61.6% SiO₂). The basaltic-andesite is relatively enriched in incompatible elements compared to the high-Al basalt — V. Colima trend.The ne-normative basanite-minette samples are highly enriched in incompatible elements, while the contemporaneous hy — qz-normative calc-alkaline suite, encompassing the high-Al basalt and V. Colima's andesites, is characterized by relatively low abundances of these elements. No likely mineral assemblage can relate the alkaline and calc-alkaline suites through crystal fractionation; they probably represent fundamentally different melting events.During the Quaternary, the main focus of andesitic volcanism in the southern Colima graben has migrated southward with time. Volcán Colima marks its present position, 5 km south of the Pleistocene volcano Nevado de Colima, and another 15 km from the still older Volcán Cantaro. The eruptions of basic alkalic magma probably occurred during the late stages of Nevado's life and through the life of V. Colima. They generally migrated from west to east with time, towards V. Cantaro. The most recent cone, V. Apaxtepec, is the only one east of the andesitic Colima-Cantaro axis. The oldest and the two youngest cones produced basanites, while minettes dominated at cones of intermediate ages. The cinder cone eruptions may have coincided with a phase of lamprophyre dike injection into plutons solidifying beneath the extinct volcanoes north of V. Colima. The southern end of the Colima graben can be viewed, then, as the volcanic analog of many classical, post-plutonic, hypabyssal lamprophyre localities.     

An experimental study of a minette from the Milk River area, southern Alberta, Canada

Buhlmann et al. (Can J Earth Sci 37: 1629–1650, 2000) studied the minettes and xenoliths from the Milk River area of southern Alberta, Canada. Based on previous work, they hypothesized that the minettes were derived from a source containing phlogopite?+?clinopyroxene?±?olivine, at pressures ≥1.7?GPa. To test this hypothesis, liquidus experiments were performed on a primitive minette between 1.33 and 2.21?GPa and between 1,300 and 1,400?°C to constrain the mineralogy of its source region. We found a multiple saturation point along the liquidus at 1.77 GPa and 1,350?°C, where the liquid coexists with orthopyroxene and olivine. Neither phlogopite nor clinopyroxene were found to be liquidus phases, which is inconsistent with Buhlmann et al.’s hypothesis. We suggest that our minette is not primary, but had re-equilibrated with harzburgitic mantle subsequent to formation. In such a scenario, partial melting of a veined source containing mica and clinopyroxene occurred at or near the base of the Wyoming craton (~200?km). Minimal heating or the introduction of hydrous fluids into the source would be required to induce partial melting. Rapid ascent rates, coupled with slow cooling rates, of the “primary minette magma” would preserve the high temperature observed in our experiments. At ~58?km, our “primary minette magma” likely stalled and re-equilibrated with the harzburgite surroundings.     

Origins of compositional heterogeneity in olivine-hosted melt inclusions from the Baffin Island picrites

The Baffin Island picrites are highly magnesian (22 wt% MgO) olivine tholeiites, erupted through felsic continental crust. Plots of most major and minor element oxides against MgO for the lavas define very tight trends consistent with modification of melts parental to the erupted suite by olivine fractionation or accumulation. However, melt inclusions trapped in primitive olivine phenocrysts in these lavas have much more diverse compositions. After correction for post-entrapment modification, the inclusions are systematically slightly lower in Al₂O₃, and significantly higher in SiO₂, K₂O and P₂O₅ than the lavas fractionation trends. CaO, Na₂O and TiO₂ contents lie within the lavas fractionation trends. Similarly, most inclusions are higher in Sr/Nd, K/Nb, Rb/Ba, Rb/Sr, U/Nb and Ba/Th than the lavas. These characteristics resulted from up to 15% contamination of evolving picritic-basaltic liquids by locally-derived, broadly granitic partial melts of the quartz + feldspar-rich crust through which the picrites erupted. Contamination was minor in the bulk lavas (<1%), suggesting that the inclusions compositions partly reflect a link between wall rock reaction and precipitation of liquidus olivine. Rapid crystallisation of liquidus olivine from the picrites, along with melting of felsic crustal wall rocks of magma chambers or conduits, were likely during emplacement of hot picritic magmas into cooler felsic crust. Inclusion compositions may thus reflect mixing trends or may be constrained to phase boundaries between olivine and a phase being resorbed, for example, an olivine-plagioclase cotectic. The extent of contamination was probably a complex function of diffusion rates of components in the magmas, and phenocryst growth rates and proximity to wall rock. These results bear on the common observation that melt inclusions compositions are frequently more heterogeneous than those of the lavas that host them.     

Magmatic evolution of Late Cenozoic volcanic rocks of the Lau Ridge,Fiji

Three main groups of lavas are exposed on islands of the Lau Ridge: the Lau Volcanic Group (LVG), 14.0–5.4 Ma, are predominantly andesite; Korobasaga Volcanic Group (KVG), 4.4–2.4 Ma, are predominantly basalt and Mago Volcanic Group (MVG), 2.0–0.3 Ma, are basalt-hawaiite. LVG and KVG lavas are mostly medium-K tholeiitic rocks with high LILE/HFSE ratios characteristic of islands ares, while MVG lavas are ne-normative alkalic rocks with high LILE and HFSE, characteristic of ocean island basalts. LVG lavas have high ?_Nd (+8.0–+8.4) and low ⁸⁷Sr/⁸⁶Sr (0.70273–0.70349) similar to N-MORB, whereas KVG lavas have slightly more radiogenic values (?_Nd=+7.5?+8.4; ⁸⁷Sr/⁸⁶Sr=0.70323-0.70397). MVG lavas form an isotopically distinct group having lower ?_Nd (+4.6–+4.9) and (⁸⁷Sr/⁸⁶Sr ranging from 0.70347–0.70375). LVG lavas were erupted in a primary oceanic island arc (Vitiaz arc) during the Miocene. Basaltic lavas were derived by approximately 19% partial melting of mantle wedge peridotite with only minor subduction component. Andesites and dacites were produced by low-pressure plagioclase-pyroxene-titanomagnetite dominated crystal fractionation. KVG lavas were erupted during the period immediately prior to or during the initial stages of rifting in the Lau Basin, and, like LVG lavas, show significant chemical differences at the northern and southern ends of the Lau Ridge. Lavas at the northern end (type (ii)) appear to be derived from a more depleted source than LVG but with a greater amount of subduction component. Those at the southern end (type (i)) probably came from a slightly more enriched source with less subduction component. MVG basalts and hawaiites were derived from an enriched mantle with little or no subduction input. The hawaiites (type (i)) could not have been derived from the basalts (type (ii)), and the two magma types must have come from different sources, indicating mantle heterogeneity. The lack of subduction influence indicates the MVG lavas are tectonically unrelated to the present-day Tonga arc, and the lack of depletion indicators suggests they have tapped a different (new?) part of the mantle wedge. This may reflect introduction of sub-Pacific mantle through the present Tonga-Lau subduction system.     

Phase equilibria of phlogopite lamprophyres from western Mexico: biotite-liquid equilibria and P-T estimates for biotite-bearing igneous rocks

 Olivine and augite minette powders have been equilibrated from one bar to nearly 2.0 kbar (water-saturated), and from 900 to 1300° C, and then quenched rapidly, at oxygen fugacities controlled between the nickel-nickel oxide (NNO) and hematite-magnetite (HM) oxygen buffers. The liquidus of both samples is suppressed ∼100° C at water-saturated conditions and 1500 bar. Both lavas contained between 3 and 4 wt% water at the stage of phenocryst precipitation. The partitioning of ferric and ferrous iron between phlogopite and liquid has been determined on eight samples across 3 log f _O2 units; when these determinations are combined with previous studies, Fe₂O₃/(Σ FeO total) of Mg-rich biotite can be calculated knowing log f _O2, T, and X _Fe. Thermodynamic modelling of biotite-liquid equilibria results in two expressions for calculating activity coefficients (γ) for annite and phlogopite in natural biotites. Based on the partitioning of BaO and TiO₂ between biotite and liquid, we have formulated a thermometer and barometer. Over the range of 400° C, TiO₂ partitioning between phlogopite and liquid is a function of temperature (±50° C), and is insensitive to pressure and H₂O and O₂ activities. BaO partitioning between phlogopite and liquid is a function of both temperature and pressure (±4 kbar), the latter being most important. Applying the TiO₂ and BaO partitioning expressions to lamprophyre and lamproite suites shows that Mexican minettes equilibrated at low pressures (5 to 15 kbar;±4 kbar) and temperatures (1090 to 1160° C; ±50° C), while Australian lamproites equilibrated at higher P (up to 30 kbar; ±4 kbar) and T (1125 to 1400° C; ±50° C). Experimental glass compositions and phenocryst fractionation calculations, together with the BaO- and TiO₂- based pressure calculations indicate that felsic minettes from the Mexican suite of lavas can be generated by simple fractionation of a more mafic parent minette at mid to lower crustal pressures. Received: 1 August 1994/Accepted: 30 June 1995     

Origin of Minette by Mixing of Lamproite and Dacite Magmas in Veliki Majdan, Serbia

Composite dykes consisting of leucominette and dacite as wellas discrete dykes and flows of minette and lamproite composition,occur in the Veliki Majdan area, western Serbia. This area ispart of the Serbian Tertiary magmatic province, which consistsof numerous small occurrences of ultrapotassic igneous rocks.The composite dykes have leucominette margins (up to 150 cmthick) enclosing a central part of dacite up to 100 m in width.Between these two lithologies, a decimetre-sized transitionzone may occur. Petrography, mineral chemistry and bulk-rockgeochemistry, including Sr, Nd and Pb isotopes, provide evidencethat the minettes and leucominettes formed by hybridizationbetween a felsic magma similar in composition to dacite anda mantle-derived lamproitic magma. The leucominettes and minettescontain all phenocryst types (biotite, plagioclase, quartz)present in the dacites, but in partly resorbed and reacted form.The mica displays a great diversity of resorption textures asa result of partial dissolution, incipient melting and phlogopitization,suggesting superheating of the felsic melt during hybridization;the mineral modes and mineral compositions of the leucominettesand minettes resemble those in the lamproites. A model for themodification of lamproite melt towards minette is presentedin which minette is formed by mixing of lamproite and <30%felsic magma. The lack of any significant correlation betweenPb isotopic ratios and some of the ‘mixing-indices’(SiO₂, Zr, Zr/Nb, ¹⁴³Nd/¹⁴⁴Nd_i) recognized in the hybridizationmodel for the Veliki Majdan dykes may be a result of similarityof the Pb-isotopic signature in the two end-members. Highlyphlogopitized biotite xenocrysts in the minettes are ascribedto the retention of volatile components after magma mixing andcrystallization of a new generation of phlogopite from the hybridizedmagma. The magma-mixing model explains the reverse zoning andresorption features of phlogopite macrocrysts commonly recognizedin calcalkaline lamprophyres elsewhere. Therefore, this mixingmechanism may be globally applicable for the origin of minettesassociated with calcalkaline granitic plutonism in post-orogenicsettings. KEY WORDS: Serbia; lamproites; micas; phlogopitization; calcalkaline lamprophyres; superheating; magma mixing     

Melting phase relations of a mica–clinopyroxenite from the Milk River area, southern Alberta, Canada

Melting experiments were conducted on a mica–clinopyroxenite xenolith brought up in a minette dyke in southern Alberta, Canada, near Milk River. Both the minettes and mica–clinopyroxenite xenoliths were studied by Buhlmann et al. (Can J Earth Sci 37:1629–1650, 2000), who hypothesized that the minettes formed by partial melting of a mantle source containing clinopyroxene + phlogopite ± olivine, at pressures ≥1.7 GPa. In liquidus experiments performed on the most primitive minette in our previous study (Funk and Luth in Contrib Mineral Petrol 164:999–1009, 2012), we found a multiple saturation point where olivine and orthopyroxene coexisted with liquid at 1.77 GPa and 1,350 °C. We argued that the minette originally formed by partial melting of clinopyroxene + phlogopite, but had re-equilibrated with a harzburgite during ascent. In the current study, we wanted to test both the source region hypothesis of Buhlmann et al. and our re-equilibration hypothesis by studying the near-solidus phase equilibria of a mica + clinopyroxene assemblage. We found the solidus for our xenolith has a steep slope in P–T space and lies at temperatures above those of a normal cratonic geotherm, implying that this mica–clinopyroxenite is stable in the cratonic mantle. Melting could occur at greater depths, where the solidus is extrapolated to cross the geotherm or must be induced either by raising the temperatures of the surrounding rocks or by introducing hydrous fluids into the source. Our melts are in equilibrium with clinopyroxene and olivine. The compositions of the liquids derived from melting this xenolith are similar to madupitic lamproites from the Leucite Hills, Wyoming, studied by Carmichael (Contrib Mineral Petrol 15:24–66, 1967) and Barton and Hamilton (Contrib Mineral Petrol 66:41–49, 1978; Contrib Mineral Petrol 69:133–142, 1979). Barton and Hamilton (Contrib Mineral Petrol 69:133–142, 1979) proposed that the madupitic lamproites may have come from a source containing mica and pyroxene. This study supports their hypothesis. The composition of the most primitive minette from southern Alberta lies between our experimental melt and a population of representative mantle orthopyroxenes. We conclude from our study that the Milk River minettes were likely derived from a source containing phlogopite, clinopyroxene and trace amounts of apatite, which formed olivine upon melting. During ascent, the melts changed composition by reacting with orthopyroxene.     

Implications of Quaternary volcanism at Cerro Tuzgle for crustal and mantle evolution of the Puna Plateau,Central Andes,Argentina

The high-K Tuzgle volcanic center, (24° S, 66.5° W) along with several small shoshonitic centers, developed along extensional Quaternary faults of the El Toro lineament on the east-central Puna plateau, 275 km east of the main front of the Andean Central Volcanic Zone (CVZ). These magmas formed by complex mixing processes in the mantle and thickened crust (>50 km) above a 200 km deep scismic zone. Tuzgle magmas are differentiated from shoshonitic series magmas by their more intraplate-like Ti group element characteristics, lower incompatible element concentrations, and lower ⁸⁷Sr/⁸⁶Sr ratios at a given Nd. Underlying Mio-Pliocene volcanic rocks erupted in a compressional stress regime and have back-arc like calc-alkaline chemical characteristics. The Tuzgle rocks can be divided into two sequences with different mantle precursors: a) an older, more voluminous rhyodacitic (ignimbrite) to mafic andestitic (56% to 71% SiO₂) sequence with La/Yb ratios <30, and b) a younger andesitic sequence with La/Yb ratios >35. La/Yb ratios are controlled by the mafic components: low ratios result from larger mantle melt percentages than high ratios. Shoshonitic series lavas (52% to 62% SiO₂) contain small percentage melts of more isotopically enriched arc-like mantle sources. Some young Tuzgle lavas have a shoshonitic-like component. Variable thermal conditions and complex stress system are required to produce the Tuzgle and shoshonitic series magmas in the same vicinity. These conditions are consistent with the underlying mantle being in transition from the thick mantle lithosphere which produced rare shoshonitic flows in the Altiplano to the thinner mantle lithosphere that produced back-are calc-alkaline and intraplate-type flows in the southern Puna. Substantial upper crustal type contamination in Tuzgle lavas is indicated by decreasing Nd (-2.5 to-6.7) with increasing ⁸⁷Sr/⁸⁶Sr (0.7063 to 0.7099) ratios and SiO₂ concentrations, and by negative Eu anomalies (Eu/Eu^* <0.78) in lavas that lack plagioclase phenocrysts. Trace element arguments indicate that the bulk contaminant was more silicic than the Tuzgle ignimbrite and left a residue with a high pressure mineralogy. Crustal shortening processes transported upper crustal contaminants to depths where melting occurred. These contaminants mixed with mafic magmas that were fractionating mafic phases at high pressure. Silicic melts formed at depth by these processes accumulated at a mid to upper crustal discontinuity (decollement). The Tuzgle ignimbrite erupted from this level when melting rates were highest. Subsequent lavas are mixtures of contaminated mafic magmas and ponded silicic melts. Feldspar and quartz phenocrysts in the lavas are phenocrysts from the ponded silicic magmas.     

Ultramafic Xenoliths from the Bearpaw Mountains, Montana, USA: Evidence for Multiple Metasomatic Events in the Lithospheric Mantle beneath the Wyoming Craton

Ultramafic xenoliths in Eocene minettes of the Bearpaw Mountainsvolcanic field (Montana, USA), derived from the lower lithosphereof the Wyoming craton, can be divided based on textural criteriainto tectonite and cumulate groups. The tectonites consist ofstrongly depleted spinel lherzolites, harzburgites and dunites.Although their mineralogical compositions are generally similarto those of spinel peridotites in off-craton settings, somecontain pyroxenes and spinels that have unusually low Al₂O₃contents more akin to those found in cratonic spinel peridotites.Furthermore, the tectonite peridotites have whole-rock majorelement compositions that tend to be significantly more depletedthan non-cratonic mantle spinel peridotites (high MgO, low CaO,Al₂O₃ and TiO₂) and resemble those of cratonic mantle. Thesecompositions could have been generated by up to 30% partialmelting of an undepleted mantle source. Petrographic evidencesuggests that the mantle beneath the Wyoming craton was re-enrichedin three ways: (1) by silicate melts that formed mica websteriteand clinopyroxenite veins; (2) by growth of phlogopite fromK-rich hydrous fluids; (3) by interaction with aqueous fluidsto form orthopyroxene porphyroblasts and orthopyroxenite veins.In contrast to their depleted major element compositions, thetectonite peridotites are mostly light rare earth element (LREE)-enrichedand show enrichment in fluid-mobile elements such as Cs, Rb,U and Pb on mantle-normalized diagrams. Lack of enrichment inhigh field strength elements (HFSE; e.g. Nb, Ta, Zr and Hf)suggests that the tectonite peridotites have been metasomatizedby a subduction-related fluid. Clinopyroxenes from the tectoniteperidotites have distinct U-shaped REE patterns with strongLREE enrichment. They have ¹⁴³Nd/¹⁴⁴Nd values that range from0·5121 (close to the host minette values) to 0·5107,similar to those of xenoliths from the nearby Highwood Mountains.Foliated mica websterites also have low ¹⁴³Nd/¹⁴⁴Nd values (0·5113)and extremely high ⁸⁷Sr/⁸⁶Sr ratios in their constituent phlogopite,indicating an ancient (probably mid-Proterozoic) enrichment.This enriched mantle lithosphere later contributed to the formationof the high-K Eocene host magmas. The cumulate group rangesfrom clinopyroxene-rich mica peridotites (including abundantmica wehrlites) to mica clinopyroxenites. Most contain >30%phlogopite. Their mineral compositions are similar to thoseof phenocrysts in the host minettes. Their whole-rock compositionsare generally poorer in MgO but richer in incompatible traceelements than those of the tectonite peridotites. Whole-rocktrace element patterns are enriched in large ion lithophileelements (LILE; Rb, Cs, U and Pb) and depleted in HFSE (Nb,Ta Zr and Hf) as in the host minettes, and their Sr–Ndisotopic compositions are also identical to those of the minettes.Their clinopyroxenes are LREE-enriched and formed in equilibriumwith a LREE-enriched melt closely resembling the minettes. Thecumulates therefore represent a much younger magmatic event,related to crystallization at mantle depths of minette magmasin Eocene times, that caused further metasomatic enrichmentof the lithosphere. KEY WORDS: ultramafic xenoliths; Montana; Wyoming craton; metasomatism; cumulates; minette     

Peralkaline nephelinites. I. Comparative petrology of Shombole and Oldoinyo L'engai,East Africa

Shombole, a nephelinite-carbonatite volcano in south Kenya, erupted silicate lavas, carbonatite dikes and tuffs, and pyroclastic rocks similar to those at other East African alkaline centres. Shombole lavas containing cpx + nepheline + accessory minerals range from perovskite-bearing nephelinites (43% SiO₂, volatile-free) to sphene-bearing and phonolitic nephelinites (46–49% SiO₂) and phonolites (49–56% SiO₂) and have low peralkalinity ([Na+K]/Al 1.15) which does not correlate with SiO₂. Early fractionation of olivine and clinopyroxene strongly depleted Ni and Cr concentrations (10 ppm); fractionation of perovskite, melanite, sphene, and apatite produced negative correlations of all REE with SiO₂. Many lavas contain cognate intrusive xenoliths and xenocrysts and oscillatory zoning is a common feature of clinopyroxene, nepheline, and melanite crystals, indicating recycling of intrusive material. Irregular calcite-rich bodies in many samples are interpreted as quenched immiscible Ca-carbonatite liquid, and [Ca-carbonate]-silicate liquid immiscibility is observed in experiments with one nephelinite. Chemical variation in the Shombole suite can be modeled as a combination of crystal fractionation (clinopyroxene and heavy minor phases) and retention of neutral density nepheline derived from disaggregated xenoliths entrained during emplacement of dike swarms. Six newly analyzed lavas from Oldoinyo L'engai, northern Tanzania, are geochemically similar to Shombole nephelinites except that they have relatively high Na₂O+K₂O (average 18% vs 12%) and Zr (average 680 ppm vs 400 ppm). They are extremely peralkaline and are not typical of nephelinites from other centres. Three with [Na+K]/Al1.5 contain euhedral wollastonite phenocrysts; three with [Na+K]/Al2.0 contain combeite (Na₂Ca₂Si₃O₉) phenocrysts and pseudomorphs after wollastonite. Both types contain abundant sodalite phenocrysts (+nepheline+clinopyroxene+melanite+sphene). Seven other wollastonite nephelinite samples from L'engai have been described, but it is a lava type rarely seen in other centres. Combeite has been described from only two other locations (Mt. Shaheru, Zaire; Mayener Feld, Eifel). The hyperalkaline L'engai nephelinites have compositions similar to those of experimental silicate liquids immiscible with natrocarbonatite. Textural evidence for both carbonate-silicate (as carbonate globules) and silicate-silicate (as two optically discrete glasses with distinct compositions) liquid immiscibility is observed in the samples.     

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     

High-Ca,low-alkali carbonatite volcanism at Fort Portal,Uganda

A Quaternary volcanic field at Fort Portal, SW Uganda, contains approximately 50 vents that erupted only carbonatite. The vents are marked by monogenetic tuff cones defining two ENE-trending belts. Lava from a fissure at the west end of the northern belt formed a flow 0.3 km² in area and 1–5 m thick. The lava is vesicular throughout with a scoriaceous top, and probably formed by agglutination of spatter from lava fountains. Phenocrysts are olivine, clinopyroxene, phlogopite, and titanomagnetite enclosing blebs of pyrrhotite. Rims of monticellite, gehlenite, and reinhardbraunsite surround olivine, clinopyroxene and phlogopite, and magnetite is rimmed by spinel. The reaction relations suggest that these phenocryst phases are actually xenocrysts, perhaps from a source similar to that which supplied phlogopite clinopyroxenite xenoliths in the Katwe-Kikorongo volcanic field 75 km SW of Fort Portal. The groundmass of fresh carbonatite lava consists of tabular calcite, spurrite, periclase, hydroxylapatite, perovskite, spinel, pyrrhotite, and barite. The lava was readily altered; where meteoric water had access, spurrite and periclase are lacking, and some calcite is recrystallized. Vesicles in lava and rare dike rocks are partly filled with calcite, followed by jennite and thaumasite. Pyroclastic deposits cover 142 km² and are far more voluminous than lava. Carbonatite ejecta were identical to lava in primary mineralogy, but are much more contaminated by crustal rock fragments and xenocrysts. At Fort Portal, eruption of a CaO-MgO-CO₂-SiO₂-P₂O₅-SO₂-H₂O-F liquid was unaccompanied by that of a more silica-rich or alkali-rich liquid. Alkali-rich carbonatite lavas and pyroclastic deposits have been documented elsewhere in East Africa, and calcite-rich volcanic carbonatites have been attributed to replacement of magmatic alkali carbonates by calcite. However, the alkali-poor volcanic carbonatites at Fort Portal were not formed by leaching of alkalis in meteoric water; tabular calcite is not pseudomorphous after alkali carbonates such as nyerereite. The Fort Portal magma was low in alkalis at the time of eruption.     

Petrology of Volcán Tequila,Jalisco, Mexico: disequilibrium phenocryst assemblages and evolution of the subvolcanic magma system

Volcán Tequila is an extinct stratovolcano in the western Mexican Volcanic Belt that has erupted lavas ranging from andesite to rhyolite during the last 0.9 Ma. Following an early period of rhyolitic volcanism, the main edifice of the volcano was constructed by central vent eruptions that produced 25 km³ of pyroxene-andesite. At about 0.2 Ma central activity ceased and numerous flows of hornblende-bearing andesite, dacite, and rhyodacite erupted from vents located around the flanks of the volcano. Bimodal plagioclase phenocryst rim compositions in lavas from both the main edifice and the flanks indicate that magma mixing commonly occurred shortly prior to or during eruption. Compositions of endmember magmas involved in mixing, as constrained by whole-rock major and trace element abundances, phenocryst compositions, and mineral-melt exchange equilibria, are similar to those of some lavas erupted from the central vent and on the flanks of the volcano. Estimated pre-eruptive temperatures for hornblende-bearing lavas (970°–830°C) are systematically lower than for lavas that lack hornblende (1045°–970°C), whereas magmatic H₂O contents are systematically higher for hornblende-bearing lavas. In addition to stabilizing hornblende, high magmatic water contents promoted crystallization of calcic plagioclase (An_70–82). Frequent injections of magma into the base of the subvolcanic plumbing system followed by eruption of mixed magma probably prevented formation of large volumes of silicic magma, which have caused paroxysmal, caldera-forming eruptions at other stratovolcanoes in western Mexico. The later stages of volcanic activity, represented by the flank lavas, indicate a change from a large magma storage reservoir to numerous small ones that developed along a NW-trending zone parallel to regional fault trends. Sr and Nd isotopic data for lavas from the Tequila region and other volcanoes in western Mexico demonstrate that differentiated calc-alkaline magmas are formed primarily through crystal fractionation of mantle-derived calc-alkaline basalt coupled with assimilation of crustal material. Present Address:Department of the Geophysical Sciences The University of Chicago, Chicago IL, 60637, USA     

Andesites from northeastern Kanaga Island,Aleutians

Kanaga island is located in the central Aleutian island arc. Northeastern Kanaga is a currently active late Tertiary to Recent calc-alkaline volcanic complex. Basaltic andesite to andesite lavas record three episodes (series) of volcanic activity. Series I and Series II lavas are all andesite while Series III lavas are basaltic andesite to andesite. Four Series II andesites contain abundant quenched magmatic inclusions ranging in composition from high-MgO low-alumina basalt to low-MgO highalumina basalt. The spectrum of lava compositions is due primarily to fractional crystallization of a parental low-MgO high-alumina basalt but with variable degrees of crustal contamination and magma mixing. The earliest Series I lavas represent mixing between high-alumina basalt and silicic andesite with maximum SiO₂ contents of 65–67 wt %. Later Series I and all Series II lavas are due to mixing of andesite magmas of similar composition. The maximum SiO₂ content of the pre-mixed andesites magmas is estimated at 60–63 wt %. The youngest lavas (Series III) are all non-mixed and have maximum estimated SiO₂ contents of 59 wt %. The earliest Series I lavas contain a significant crustal component while all later lavas do not. It is concluded that the maximum SiO₂ contents of silicic magmas, the contribution of crustal material to silicic magma generation, and the role of magma mixing all decrease with time. Furthermore, silicic magmas generated by fractional crystallization at this volcanic center have a maximum SiO₂ content of 63 wt %. All of these features have also been documented at the central Aleutian Cold Bay Volcanic Center (Brophy 1987). Based on data from these two centers a model of Aleutian calc-alkaline magma chamber development is proposed. The main features are: (1) a single low pressure magma chamber is continuously supplied by primitive low-alumina basalt; (2) non-primary high-alumina basalt is formed along the chamber margins by selective gravitational settling of olivine and clinopyroxene and retention of plagioclase; (3) sidewall crystallization accompanied by crustal melting produces buoyant silicic (>63 wt % SiO₂) liquids that pond at the top of the chamber, and; (4) continued sidewall crystallization, now isolated from the chamber wall, produces silicic liquids with 63 wt % SiO₂ that increase the thickness and lowers the overall SiO₂ content of the upper silicic zone. It is suggested that the maximum SiO₂ content of 63% imposed on fractionation-generated magmas is due to a rheological barrier that prohibits the extraction of more silicic liquids from a crystal-liquid mush along the chamber wall.     

Petrology and genesis of natrocarbonatite

Microprobe analyses of phenocrysts and groundmass, and crystal-size distributions of phenocrysts of pahoehoe natrocarbonatite lavas of the 1963 eruption of Oldoinyo Lengai have been determined. Nyerereite phenocrysts are homogeneous, with average composition Nc₄₁Kc₉Cc₅₀ (neglecting F, Cl, P₂O₅, and SO₃) where Nc=Na₂CO₃, Kc=K₂CO₃, and Cc= (Ca,Sr)CO₃. Gregoryite phenocrysts have turbid, pale brown, oscillatorily zoned cores (average composition Nc₇₇Kc₅Cc₁₈) with 0–30% oriented inclusions of exsolved nyerereite. Overgrowths on gregoryites (30 m wide) are relatively sodic (Nc₈₁Kc₄Cc₁₅) and are free of inclusions. Cores and rims are rich in SO₃ (4%) and P₂O₅ (2%). Blebs of pyrite-alabandite mixtures (100 m) occur in the groundmass. The groundmass has the simplified composition Nc₆₅Kc₁₅Cc₂₀, less calcic than the composition of the 1-kbar nyerereite+gregoryite +liquid cotectic in the ternary system Nc-Kc-Cc. Groundmass quench growth of alkali halides + carbonate was followed by slower growth of coarse-grained and irregular gregoryite +KCl+BaCO₃. Crystal size distributions of gregoryite and nyerereite in one sample are linear, implying little loss or gain of phenocrysts by crystal settling. AverageG is 0.15 mm, compared toG=0.03 mm for combeite phenocrysts from consanguineous nephelinite. Assuming an equal residence time () for both lavas, the apparent crystal growth rate (G) in carbonate melt is 5 times greater than in peralkaline undersaturated silicate melt. Data from experiments with natrocarbonatite and related synthetic systems indicate that Na–K–Ca carbonatite magmas which crystallize calcite cannot fractionate to nyerereite+gregoryite +liquid assemblages. Natrocarbonatites plot in the liquidus field of nyerereite, and minor fractionation of nyerereite to produce the erupted lavas is indicated. The term natrocarbonatite has been inappropriately applied to other eruptive rocks with calcite phenocrysts, and the only known occurrence of gregoryite-bearing natrocarbonatite is Oldoinyo Lengai. Natrocarbonatite probably originates by liquid immiscibility from strongly peralkaline nephelinites, which have also been erupted at Oldoinyo Lengai.     

Lamprophyric lavas in the Colima graben,SW Mexico

The Colima graben, located in SW Mexico, is one of three grabens which intersect about 50 km SSW of Guadalajara, forming a triple junction. The 90 km long, 20–60 km wide Colima graben represents a N-S rift of the E-W trending Mexican Volcanic Belt. Since the Early Pliocene, the Colima graben has served as a locus for the eruption of alkaline lavas, the most recent of which are basanites and minettes erupted from Late Pleistocene cinder cones (Luhr and Carmichael 1981). In this paper, we report on older alkaline lavas which crop out in the graben's walls. These rocks include phlogopite- and hornblende-bearing lamprophyres, a phlogopite-kalsilite-ankaratrite, and high-K andesites. These lavas crop out throughout the Colima graben area, and are intimately associated with calc-alkaline lavas in the field. Compared to these, the alkaline rocks are strikingly enriched in the incompatible elements, particularly Ba, Sr, P, and the LREE. Unlike the younger Late Pleistocene alkaline cinder cone lavas, most of the graben wall lamprophyres and the high-K andesites represent magmas that appear to have undergone significant evolution since their generation, including fractionation, crustal contamination, and possible magma mixing. Least-squares modeling indicates that the cinder cone minettes represent reasonable parental magmas for the graben lamprophyres. The occurrence of these alkaline lavas in an active calc-alkaline volcanic arc is unusual, and we suggest that they are a manifestation of the rifting processes which produced the Colima graben.