Metasomatism of sub-arc mantle peridotites below southernmost South America: reduction of<Emphasis Type="Italic"> f</Emphasis>O<Subscript>2</Subscript> by slab-melt

Quaternary basalts in the Cerro del Fraile area contain two types of mantle xenoliths; coarse-grained (2–5 mm) C-type spinel harzburgites and lherzolites, and fine-grained (0.5–2 mm) intensely metasomatized F-type spinel lherzolites. C-type xenoliths have high Mg in olivine (Fo = 90–91) and a range in Cr# [Cr/ (Cr + Al) = 0.17–0.34] in spinel. Two C-type samples contain websterite veinlets and solidified patches of melt that is now composed of minute quenched grains of plagioclase + Cr-spinel + clinopyroxene + olivine. These patches of quenched melts are formed by decompression melting of pargasitic amphibole. High Ti contents and common occurrence of relic Cr-spinel in the quenched melts indicate that the amphibole is formed from spinel by interaction with the Ti-rich parental magma of the websterite veinlets. The fO₂ values of these two C-type xenoliths range from ΔFMQ −0.2 to −0.4, which is consistent with their metasomatism by an asthenospheric mantle-derived melt. The rest of the C-type samples are free of “melt,” but show cryptic metasomatism by slab-derived aqueous fluids, which produced high concentrations of fluid-mobile elements in clinopyroxenes, and higher fO₂ ranging from ΔFMQ +0.1 to +0.3. F-type lherzolites are intensely metasomatized to form spinel with low Cr# (∼0.13) and silicate minerals with low MgO, olivine (Fo = ∼84), orthpyroxene [Mg# = Mg/(Mg + ΣFe) = ∼0.86] and clinopyroxene (Mg# = ∼0.88). Patches of “melt” are common in all F-type samples and their compositions are similar to pargasitic amphibole with low TiO₂ (<0.56 wt%), Cr₂O₃ (<0.55 wt%) and MgO (<16.3 wt%). Low Mg# values of silicate minerals, including the amphibole, suggest that the metasomatic agent is most likely a slab melt. This is supported by high ratios of Sr/Y and light rare earth elements (REE)/heavy REE in clinopyroxenes. F-type xenoliths show relatively low fO₂ (ΔFMQ −0.9 to −1.1) compared to C-type xenoliths and this is explained by the fusion of organic-rich sediments overlying the slab during the slab melt. Trench-fill sediments in the area are high in organic matter. The fusion of such wet sediments likely produced CH₄-rich fluids and reduced melts that mixed with the slab melt. High U and Th in bulk rocks and clinopyroxene in F-type xenoliths support the proposed interpretation.     

Petrogenesis of ultramafic and mafic xenoliths from Mesozoic basanites in southern Sweden: constraints from mineral chemistry

Jurassic basanite necks occurring at the junction of two major fault zones in Scania contain ultramafic (peridotites, pyroxenites) and mafic xenoliths, which together indicate a diversity of upper mantle and lower crustal assemblages beneath this region. The peridotites can be subdivided into lherzolites, dunites and harzburgites. Most lherzolites are porphyroclastic, containing orthopyroxene and olivine porphyroclasts. They consist of Mg-rich silicates (Mg# = Mg/(Mg + Fe_tot) × 100; 88–94) and vermicular spinel. Calculated equilibration temperatures are lower in porphyroclastic lherzolites (975–1,007°C) than in equigranular lherzolite (1,079°C), indicating an origin from different parts of the upper mantle. According to the spinel composition the lherzolites represent residues of 8–13% fractional melting. They are similar in texture, mineralogy and major element composition to mantle xenoliths from Cenozoic Central European volcanic fields. Dunitic and harzburgitic peridotites are equigranular and only slightly deformed. Silicate minerals have lower to similar Mg# (83–92) as lherzolites and lack primary spinel. Resorbed patches in dunite and harzburgite xenoliths might be the remnants of metasomatic processes that changed the upper mantle composition. Pyroxenites are coarse, undeformed and have silicate minerals with partly lower Mg# than peridotites (70–91). Pyroxenitic oxides are pleonaste spinels. According to two-pyroxene thermometry pyroxenites show a large range of equilibration temperatures (919–1,280°C). In contrast, mafic xenoliths, which are mostly layered gabbronorites with pyroxene- and plagioclase-rich layers, have a narrow range of equilibration temperatures (828–890°C). These temperature ranges, together with geochemical evidence, indicate that pyroxenites and gabbroic xenoliths represent mafic intrusions within the Fennoscandian crust.     

The origin of high-Mg magmas in Mt Shasta and Medicine Lake volcanoes,Cascade Arc (California): higher and lower than mantle oxygen isotope signatures attributed to current and past subduction

We report the oxygen isotope composition of olivine and orthopyroxene phenocrysts in lavas from the main magma types at Mt Shasta and Medicine Lake Volcanoes: primitive high-alumina olivine tholeiite (HAOT), basaltic andesites (BA), primitive magnesian andesites (PMA), and dacites. The most primitive HAOT (MgO > 9 wt%) from Mt. Shasta has olivine δ¹⁸O (δ¹⁸O_Ol) values of 5.9–6.1‰, which are about 1‰ higher than those observed in olivine from normal mantle-derived magmas. In contrast, HAOT lavas from Medicine Lake have δ¹⁸O_Ol values ranging from 4.7 to 5.5‰, which are similar to or lower than values for olivine in equilibrium with mantle-derived magmas. Other magma types from both volcanoes show intermediate δ¹⁸O_Ol values. The oxygen isotope composition of the most magnesian lavas cannot be explained by crustal contamination and the trace element composition of olivine phenocrysts precludes a pyroxenitic mantle source. Therefore, the high and variable δ¹⁸O_Ol signature of the most magnesian samples studied (HAOT and BA) comes from the peridotitic mantle wedge itself. As HAOT magma is generated by anhydrous adiabatic partial melting of the shallow mantle, its 1.4‰ range in δ¹⁸O_Ol reflects a heterogeneous composition of the shallow mantle source that has been influenced by subduction fluids and/or melts sometime in the past. Magmas generated in the mantle wedge by flux melting due to modern subduction fluids, as exemplified by BA and probably PMA, display more homogeneous composition with only 0.5‰ variation. The high-δ¹⁸O values observed in magnesian lavas, and principally in the HAOT, are difficult to explain by a single-stage flux-melting process in the mantle wedge above the modern subduction zone and require a mantle source enriched in ¹⁸O. It is here explained by flow of older, pre-enriched portions of the mantle through the slab window beneath the South Cascades.     

Fine-grained mafic bodies as preserved portions of magma replenishing layered intrusions: the Nadezhda gabbronorite body, Lukkulaisvaara intrusion, Fennoscandian Shield, Russia

Summary The 100 m thick and 700 m long Nadezhda body in the Lukkulaisvaara layered intrusion exhibits concentric zonation with an inward progression from a 0.5 to 1.0 m thick marginal layer of medium- to coarse-grained norites and gabbronorites that abruptly give way to fine-grained oikocrystic gabbronorites composing the rest of the body. The concentric zonation is additionally emphasized by well-developed alignment of plagioclase laths and orthopyroxene oikocrysts parallel to the outer contacts of the body, pegmatitic gabbronorite segregations in the centre of the body and slight inward decrease in whole-rock Mg# and Cr and increase in incompatible elements. The body has distinctly higher whole-rock Mg# and lower concentrations of all incompatible components than its host rocks. It is enveloped by highly altered marginal anorthosites belonging to host norites and gabbronorites. We interpret the Nadezhda body as a portion of high Mg# (∼75%) and incompatible element-poor (∼20 ppm, Zr; ∼10 ppm, total REE; ∼0.20 wt%, TiO₂) magma that replenished the evolving chamber and became trapped within the cumulate pile. Recrystallization of adjacent rocks by volatiles exsolved from the magma upon emplacement resulted in formation of marginal anorthosites. Upon cooling the magma started to crystallize medium- to coarse-grained norites along its margins, but subsequent decompression and loss of volatiles led to rapid crystallization of magma into fine-grained oikocrystic gabbronorites. Solidification of the remaining residual liquid gave rise to pegmatitic gabbronorite segregations. Supplementary material to this paper is available in electronic form at Tables 3–6 available as electronic supplementary material Authors’ addresses: R. M. Latypov, S. Yu. Chistyakova, Kola Science Centre, Geological Institute, Fersman Str. 16, 184200 Apatity, Russia; Present address: Department of Geosciences, University of Oulu, P.O. Box 3000, Oulu, FIN-90014, Finland; T. T. Alapieti, Department of Geosciences, University of Oulu, P.O. Box 3000, Oulu, FIN-90014, Finland     

Petrology,age, and polychronous sources of the initial magmatism of the Imandra-Varzuga paleorift,Fennoscandian shield

This paper reports new geochemical and isotope data on the volcanogenic complexes of the Arvarench sequence of the Imandra-Varzuga paleorift structure of the Fennoscandian shield. It was established that these complexes are made up of komatiites, basalts, high-Mg andesites, and dacites and occupy a Sumian chronostratigraphic position with U-Pb (SHRIMP) age of 2429 ± 6.6 Ma in the regional Early Precambrian stratigraphic scale of the Kola-Norwegian province of the Fennoscandian shield, thus constraining the Sumian Subhorizon of the Lower Karelian Complex of the Northeastern Fennoscandian shield within 2450–2430 Ma. The high negative ε_Nd, LREE enrichment, and the presence of different-age Archean zircons with REE patterns indicative of disequilibrium crystallization suggest that the parental dacitic melts were derived by anatectic melting of polychronous (3.2, 2.9, 2.8, 2.7 Ga) lithological complexes of the Archean continental crust of the Kola-Norwegian province of the Fennoscandian shield. Numerical petrological-geochemical modeling of generation and evolution of primary melts of the metavolcanic rocks made it possible to establish that the isotope-geochemical peculiarities of the komatiites, basalts, and basaltic andesites can be best described by fractional crystallization of primary komatiite melt contaminated by ∼ 2% of the Archean crustal material of tonalitic composition. The mantle protolith of primary melt in terms of its isotope-geochemical parameters was similar to the “enriched” mantle source of the Paleoproterozoic (2430–2450 Ma) mafic-ultramafic layered intrusions of the Kola-Norwegian province and Sumian metavolcanic rocks of the Fennoscandian shield. The high-Mg andesites of the Arvarench sequence were derived by fractionation of crustally contaminated (∼ 2%) magnesian basalts with elevated Al content (Al₂O₃ ∼ 15.6 wt %) in equilibrium with 40–50% Cpx ₄₀-Ol ₂₀-Opx ₁₀-Pl ₁₀-Mag ₂₀ assemblage at P < 1 GPa. Obtained isotope-geochemical data and modeling results could be interpreted by off-subduction geodynamic model of the evolution of mantle plume and its interaction with the Archean continental lithosphere at the early stage of intracratonic rifting.     

Triassic Nb-enriched basalts, magnesian andesites, and adakites of the Qiangtang terrane (Central Tibet): evidence for metasomatism by slab-derived melts in the mantle wedge

New chronological, geochemical, and isotopic data are reported for Triassic (219–236 Ma) adakite-magnesian andesite-Nb-enriched basaltic rock associations from the Tuotuohe area, central Qiangtang terrane. The adakites and magnesian andesites are characterized by high Sr/Y (25–45), La/Yb (14–42) and Na₂O/K₂O (12–49) ratios, high Al₂O₃ (15.34–18.28 wt%) and moderate to high Sr concentrations (220–498 ppm) and ε_ND (t) (+0.86 to +1.21) values. Low enrichments of Th, Rb relative to Nb, and subequal normalized Nb and La contents, and enrichments of light rare earth elements combine to distinguish a group of Nb-enriched basaltic rocks (NEBs). They have positive ε_ND (t) (+2.57 to +5.16) values. Positive correlations between Th, La and Nb and an absence of negative Nb anomalies on mantle normalized plots indicate the NEBs are products of a mantle source metasomatized by a slab melt rather than by hydrous fluids. A continuous compositional variation between adakites and magnesian andesites confirms slab melt interaction with mantle peridotite. The spatial association of the NEBs with adakites and magnesian andesites define an “adakitic metasomatic volcanic series” recognized in many demonstrably subduction-related environments (e.g., Mindanao arc, Philippines; Kamchatka arc, Russia; and southern Baja California arc, Mexico). The age of the Touhuohe suite, and its correlation with Triassic NEB to the north indicates that volcanism derived from subduction-modified mantle was abundant prior to 220 Ma in the central Qiangtang terrane.     

Redox potential of mantle magmatic systems

A new variant of the olivine-clinopyroxene-spinel oxygen barometer was developed on the basis of the equilibrium 3CaMgSi₂O₆(Cpx) + 2Fe₃O₄(Spl) = 3CaMgSiO₄(Ol) + 3Fe₂SiO₄(Ol) + O₂. Oxygen fugacity was estimated for the mineral assemblages of meymechites, olivine-bearing rocks of the Guli intrusion, and olivine and clinopyroxene microphenocrysts from interstitial glasses in mantle xenoliths containing metal alloys from Sal Island, Cape Verde Archipelago. It was shown that oxygen fugacity may vary in mantlederived magmatic systems by 7–8 orders of magnitude. Thermodynamic analysis showed that the low water activity in the lower part of the subcratonic lithosphere prevents the formation of hydrocarbons even at the presence of elemental carbon and low oxygen fugacity. The most probable mechanism of diamond formation is the reduction of carbonate components in the composition of near-solidus melts coming into the lithosphere from ascending mantle plumes.     

An overview on geochemistry of Proterozoic massif-type anorthosites and associated rocks

A critical study of 311 published WR chemical analyses, isotopic and mineral chemistry of anorthosites and associated rocks from eight Proterozoic massif anorthosite complexes of India, North America and Norway indicates marked similarities in mineralogy and chemistry among similar rock types. The anorthosite and mafic-leucomafic rocks (e.g., leuconorite, leucogabbro, leucotroctolite, anorthositic gabbro, gabbroic anorthosite, etc.) constituting the major part of the massifs are characterized by higher Na₂O + K₂O, Al₂O₃, SiO₂, Mg# and Sr contents, low in plagioclase incompatible elements and REE with positive Eu anomalies. Their δ ¹⁸O‰ (5.7–7.5), initial ⁸⁷Sr/⁸⁶Sr (0.7034–0.7066) and ɛ _Nd values (+1.14 to +5.5) suggest a depleted mantle origin. The Fe-rich dioritic rocks occurring at the margin of massifs have isotopic, chemical and mineral composition more close to anorthosite-mafic-leucomafic rocks. However, there is a gradual decrease in plagioclase content, An content of plagioclase and X_Mg of orthopyroxene, and an increase in mafic silicates, oxide minerals content, plagioclase incompatible elements and REE from anorthosite-mafic-leucomafic rocks to Fe-rich dioritic rocks. The Fe-rich dioritic rocks are interpreted as residual melt from mantle derived high-Al gabbro melt, which produced the anorthosite and mafic-leucomafic rocks. Mineralogically and chemically, the K-rich felsic rocks are distinct from anorthosite-mafic-leucomafic-Fe-rich dioritic suite. They have higher δ ¹⁸O values (6.8–10.8‰) and initial ⁸⁷Sr/⁸⁶Sr (0.7067–0.7104). By contrast, the K-rich felsic suites are products of melting of crustal precursors.     

Age, composition, sources, and geodynamic environments of the origin of granitoids in the northern part of the Ozernaya zone, western Mongolia: Growth mechanisms of the Paleozoic continental crust

The paper presents data on the structure, composition, and age of granitoid associations (Tokhtogeshil’skii Complex) composing the Kharanur and Sharatologoi polychronous plutons in the northern part of the Ozernala zone in western Mongolia. The Tokhtogeshil’skii Complex was determined to consist of a number of independent magmatic associations, which were formed at 540–450 Ma, within three age intervals (540–520, 510–485, and 475–450 Ma), have different composition, were derived from different sources, and were emplaced in different geodynamic environments. During the first, island-arc stage (540–520 Ma), high-Al plagiogranites were produced, which belong to tonalite-plagiogranite (531 ± 10 Ma) and diorite (529 ±6 Ma) associations in the Kharanur pluton, low-Al plagiogranites of the tonalite-plagiogranite association (519 ± 8 Ma) in the Sharatologoi pluton, and rocks of the Khirgisnur peridotite-pyroxenite-gabbronorite complex (Kharachulu and Dzabkhan massifs). The rocks of the diorite and plagiogranite associations of the Kharanur pluton have ɛ_Nd(T) from +7.9 to +7.4, T_Nd(DM) = 0.65 Ga, and (⁸⁷Sr/⁸⁶Sr)₀ = 0.7038–0.7039. The plagiogranites of the Sharatologoi pluton (tonalite-plagiogranite association) are characterized by ɛ_Nd(T) from +6.5 to +6.6, T_Nd(DM) = 0.73–0.70 Ga, and (⁸⁷Sr/⁸⁶Sr)₀ = 0.7038–0.7039, which suggest predominantly juvenile subduction sources of the parental melts at a subordinate role of ancient crustal material. During the second, accretionary stage (510–485 Ma), low-Al plagiogranites of the diorite-tonalite-plagiogranite association of the Sharatologoi pluton (494 ± 10 Ma, M type) were formed. The Sr-Nd isotopic characteristics of these rocks ɛ_Nd(T) = +6.6, (⁸⁷Sr/⁸⁶Sr)₀ = 0.7039 are analogous to those of the plagiogranitoids of the early type. This suggests that the melted sources were similar in composition. During the third, postcollisional stage (475–450 Ma), rocks of the diorite-granodiorite-granite association were formed (459 ± 10 Ma, type I) in the Kharanur pluton. These rocks have ɛ_Nd(T) = +5.1, T_Nd(DM) = 0.74 Ga, and (⁸⁷Sr/⁸⁶Sr)₀ = 0.7096. The parental melts were supposedly derived by means of partial melting of “the Caledonian” juvenile crust with the addition of more ancient crustal material.     

Dunite Formation Processes in Highly Depleted Peridotite: Case Study of the Iwanaidake Peridotite, Hokkaido, Japan

Dunite formation processes in highly depleted peridotites arediscussed based upon a detailed study of the Iwanaidake peridotite,Hokkaido, Japan, which consists mainly of harzburgite with asmall amount of dunite. In the harzburgites, the Mg# [= 100x Mg/(Mg + Fe²⁺)] of olivine ranges from 91·5 to 92·5,and the Cr# [= 100 x Cr/(Cr + Al)] of spinel from 30 to 70;in the dunites, the Mg# of olivine ranges from 92·5 to94 and the Cr# of spinel from 60 to 85, respectively. The NiOwt % of olivine in harzburgites ranges from 0·38 to 0·44,and in dunites from 0·35 to 0·37. The Mg# andCr# are higher and NiO wt % is lower in the dunites than inthe harzburgites surrounding the dunites. The Mg# and Cr# exhibitnormal depletion trends expected from simple partial melting,whereas the NiO wt % shows an abnormal trend. On the basis ofmass balance calculations, dunites are considered to be derivedfrom the harzburgites by a process involving incongruent meltingof orthopyroxene (orthopyroxene olivine + Si-rich melt). Hydrousconditions were necessary to lower the solidus, and thus meltingof harzburgite was probably triggered by the introduction ofhydrous silicate melt. The dunite in this massif may have formedin the mantle wedge above a subduction zone. KEY WORDS: depleted peridotite; hydrous melt; incongruent melting; residual dunite; Iwanaidake peridotite     

Evidence for adiabatic decompression melting in the Southern Mariana Arc from high-Mg lavas and melt inclusions

Unusually magnesian (Mg# ∼76) basalts have been sampled from a small submarine volcano situated on the Mariana arc magmatic front. Total alkalis range from 1.7 to 1.94%, Al₂O₃ from 9.09 to 10.3% and CaO from 13.9 to 14.09%. These lavas can be classified based on mineralogy as picrite and ankaramite. Olivine-hosted melt inclusions (MIs) have median MgO contents of 17.17–17.86 wt%, 0.35–0.5% TiO₂, 42–50% SiO₂ and 1.66–3.43% total alkalis, which suggest that the parental magmas were primitive mantle melts. Trace element concentrations for both MIs and lavas are arc-like, although more depleted than most arc lavas. Chlorine (182–334 ppm) and H₂O contents (0.11–0.64 wt%) in the MIs are consistent with the estimated median oxygen fugacities (log ΔFMQ of + 1.53–1.66) which lie at the low end of the range estimates for arc basalts and picrites (ΔFMQ = + 1 to + 3). Isotopic compositions of Sr, Nd, Hf and Pb are similar to those of other Mariana arc lavas and indicate derivation from an Indian Ocean mantle domain. The averaged magmatic temperature estimate from several geothermometers was 1,367°C at 1–1.5 GPa. We propose that high-Mg magmagenesis in this region results from the adiabatic decompression melting of relatively anhydrous but metasomatized mantle wedge. This melting is attributed to enhanced upwelling related to unusual tectonics on the over-riding plate related to a tear or other discontinuity on the subducted slab.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

Modelling phase–assemblage diagrams for magnesian metapelites in the system K2O–FeO–MgO–Al2O3–SiO2–H2O: geodynamic consequences for the Monte Rosa nappe, Western Alps

Magnesian metamorphic rocks with metapelitic mineral assemblage and composition are of great interest in metamorphic petrology for their ability to constrain P–T conditions in terranes where metamorphism is not easily visible. Phase–assemblage diagrams for natural and model magnesian metapelites in the system KFMASH are presented to document how phase relationships respond to water activity, bulk composition, pressure and temperature. The phase assemblages displayed on these phase diagrams are consistent with natural mineral assemblages occurring in magnesian metapelites. It is shown that the equilibrium assemblages at high pressure conditions are very sensitive to a(H₂O). Specifically, the appearance of the characteristic HP assemblage chloritoid–talc–phengite–quartz (with excess H₂O) in the magnesian metapelites of the Monte Rosa nappe (Western Alps) is due to the reduction of a(H₂O). Furthermore, the mineral assemblages are determined by the whole-rock FeO/(FeO+MgO) ratio and effective Al content X _A as well as P and T. The predicted mineral associations for the low- and high-X _A model bulk compositions of magnesian metapelites at high pressure are not dependent on the X _A variations as they show a similar sequence of mineral assemblages. Above 20 kbar, the prograde sequence of assemblages associated with phengite (with excess SiO₂ and H₂O) for low- and high-X _A bulk compositions of magnesian metapelites is: carpholite–chlorite → chlorite–chloritoid → chloritoid–talc → chloritoid–talc–kyanite → talc–garnet–kyanite → garnet–kyanite ± biotite. At low to medium P–T conditions, a low-X _A stabilises the phengite-bearing assemblages associated with chlorite, chlorite + K-feldspar and chlorite + biotite while a high-X _A results in the chlorite–phengite bearing assemblages associated with pyrophyllite, andalusite, kyanite and carpholite. A high-X _A magnesian metapelite with nearly iron-free content stabilises the talc–kyanite–phengite assemblage at moderate to high P–T conditions. Taking into account the effective bulk composition and a(H₂O) involved in the metamorphic history, the phase–assemblage diagrams presented here may be applied to all magnesian metapelites that have compositions within the system KFMASH and therefore may contribute to gaining insights into the metamorphic evolution of terranes. As an example, the magnesian metapelites of the Monte Rosa nappe have been investigated, and an exhumation path with P–T conditions for the western roof of the Monte Rosa nappe has been derived for the first time. The exhumation shows first a near-isothermal decompression from the Alpine eclogite peak conditions around 24 kbar and 505°C down to approximately 8 kbar and 475°C followed by a second decompression with concomitant cooling.M. Frey: deceased     

Geology and petrology of the lava complex of Young Shiveluch Volcano, Kamchatka

Detailed geological and petrological-geochemical study of rocks of the lava complex of Young Shiveluch volcano made it possible to evaluate the lava volumes, the relative sequence in which the volcanic edifice was formed, and the minimum age of the onset of eruptive activity. The lavas of Young Shiveluch are predominantly magnesian andesites and basaltic andesites of a mildly potassic calc-alkaline series (SiO₂ = 55.0–63.5 wt %, Mg# = 55.5–68.9). Geologic relations and data on the mineralogy and geochemistry of rocks composing the lava complex led us to conclude that the magnesian andesites of Young Shiveluch volcano are of hybrid genesis and are a mixture of silicic derivatives and a highly magnesian magma that was periodically replenished in the shallow-depth magmatic chamber. The fractional crystallization of plagioclase and hornblende at the incomplete segregation of plagioclase crystals from the fractionating magmas resulted in adakitic geochemical parameters (Sr/Y = 50–71, Y < 18 ppm) of the most evolved rock varieties. Our results explain the genesis of the rock series of Young Shiveluch volcano without invoking a model of the melting of the subducting Pacific slab at its edge.     

Mafic magmas from Mount Baker in the northern Cascade arc,Washington: probes into mantle and crustal processes

Five mafic lava flows located on the southern flank of Mount Baker are among the most primitive in the volcanic field. A comprehensive dataset of whole rock and mineral chemistry reveals the diversity of these mafic lavas that come from distinct sources and have been variably affected by ascent through the crust. Disequilibrium textures present in all of the lavas indicate that crustal processes have affected the magmas. Despite this evidence, mantle source characteristics have been retained and three primitive endmember lava types are represented. These include (1) modified low-K tholeiitic basalt (LKOT-like), (2) typical calc-alkaline (CA) lavas, and (3) high-Mg basaltic andesite and andesite (HMBA and HMA). The Type 1 endmember, the basalt of Park Butte (49.3–50.3 wt% SiO₂, Mg# 64–65), has major element chemistry similar to LKOT found elsewhere in the Cascades. Park Butte also has the lowest overall abundances of trace elements (with the exception of the HREE), indicating it is either derived from the most depleted mantle source or has undergone the largest degree of partial melting. The Type 2 endmember is represented by the basalts of Lake Shannon (50.7–52.6 wt% SiO₂, Mg# 58–62) and Sulphur Creek (51.2–54.6 wt% SiO₂, Mg# 56–57). These two lavas are comparable to calc-alkaline rocks found in arcs worldwide and have similar trace element patterns; however, they differ from each other in abundances of REE, indicating variation in degree of partial melting or fractionation. The Type 3 endmember is represented by the HMBA of Tarn Plateau (51.8–54.0 wt% SiO₂, Mg# 68–70) and the HMA of Glacier Creek (58.3–58.7 wt% SiO₂, Mg# 63–64). The strongly depleted HREE nature of these Type 3 units and their decreasing Mg# with increasing SiO₂ suggests fractionation from a high-Mg basaltic parent derived from a source with residual garnet. Another basaltic andesite unit, Cathedral Crag (52.2–52.6 wt% SiO₂, Mg# 55–58), is an Mg-poor differentiate of the Type 3 endmember. The calc-alkaline lavas are least enriched in a subduction component (lowest H₂O, Sr/P_N, and Ba/Nb), the LKOT-like lavas are intermediate (moderate Sr/P_N and Ba/Nb), and the HMBA are most enriched (highest H₂O, Sr/P_N and Ba/Nb). The generation of the LKOT-like and calc-alkaline lavas can be successfully modeled by partial melting of a spinel lherzolite with variability in composition of slab flux and/or mantle source depletion. The HMBA lavas can be successfully modeled by partial melting of a garnet lherzolite with slab flux compositionally similar to the other lava types, or less likely by partial melting of a spinel lherzolite with a distinctly different, HREE-depleted slab flux.     

Magnesian andesites in north Xinjiang,China

Middle Devonian magnesian andesites (MAs) are widely distributed in south Altay and Carboniferous MAs are present in Alataoshan and west- and east-Tianshan in the north Xinjiang region. These MAs are andesitic rocks with 53–65% SiO₂,<1% (0.21–1.08%; average of 0.72%) TiO₂, and ≥50 Mg^#. Magnesian dacites and diorites, with 52.38–66.91% SiO₂, <0.30% TiO₂ and ≥42 Mg^# commonly occur with these MAs. Relative to boninites, MAs have lower MgO contents (average 6.39%) but higher Ti, K and Na. They have characteristic flat chondrite-normalized REE patterns with weak to no Eu anomalies (Eu depletion, or Eu/Eu* = 0.65–1.15), low (La/Yb)_N (0.98–6.4, mostly 4±) and low total REE contents (15–95 ppm). They also have high contents of compatible elements Cr and Ni (72–790 and 29–276 ppm, respectively). Their relative depletion in high field strength elements Nb, Ta and Ti, and relative enrichment in mobile large-ion lithophile elements Rb, K and Pb are evident on primitive mantle-normalized trace element spidergrams. If magnesian andesites are melts coming from the subducted oceanic crust, as proposed elsewhere, then the relatively high Y contents (>15 ppm), low Sr/Y ratios (4.4–6.2), low (La/Yb)N, and high Mg^# of the MAs in north Xinjiang provide evidence of interaction of such melts with mantle wedge peridotite. New petrographic, chemical and isotopic [(¹⁴³Nd/¹⁴⁴Nd)I = 0.51221–0.51255 (εNd(t) +0.28 to +7.2); (⁸⁷Sr/⁸⁶Sr)I = 0.7029–0.7065] data suggest that the petrogenesis of the MAs in the north Xinjiang region may have involved: (1) multiple source materials including subducted oceanic slab, juvenile crustal materials (mainly volcanic-volcanoclassic rocks with low maturity and clear mantle geochemical signatures) coming from the forearc accretionary prism and mantle wedge peridotite; (2) a combination of different petrogenetic processes including partial melting of subducted oceanic slab and juvenile crustal materials, followed by interaction of slab melts with the mantle wedge peridotite; (3) high geothermal gradient creating a high temperature (>1,000°C) environment in a volatile-rich source region; (4) unique tectonic settings including oblique subduction, slab break off resulting in slab window formation and asthenosphere upwelling, and subduction erosion resulting in transfer of forearc accretionary materials into the source region of MA magma.     

Geochemical structure of the Yoko-Dovyren layered dunite-troctolite-gabbro-norite massif,northern Baikal area

The application of the principle and algorithm of the cluster analysis of rock compositions in magmatic complexes, which were described elsewhere, made it possible to reveal the spaceless and spatial geochemical structure of the Yoko-Dovyren layered mafic-ultramafic massif. The diversity of rocks composing this intrusion was demonstrated to comprise eleven discrete geochemical types (clusters): dunites, harzburgites, melanotroctolites, troctolites, two types of olivine gabbro, two types of olivine gabbronorites, quartz gabbronorites, and granophyres. These geochemical types of rocks and the corresponding fractionation parameters (the iron atomic fraction f of mafic minerals and the anorthite concentration An of plagioclase) define a succession corresponding to the tendencies in the crystallization of a magma of respective composition. This geochemical succession is in complete agreement with the succession in which rocks were formed in the intrusion (from dunite in its bottom part to quartz gabbronorites and granophyres near its roof) and is complicated by cyclical repetitions. The main tendency revealed in the cyclic layering is as follows: cyclical intercalations consist of rocks corresponding to the neighboring members of the rock succession (plagiodunites and melanotroctolites, melanotroctolites and troctolites, troctolites and olivine gabbro, olivine gabbro and olivine gabbronorites). These tendencies are closely similar to those identified in the Kivakka intrusion, a fact suggesting that these tendencies can be common for all layered complexes of mafic and ultramafic rocks. Original Russian Text ? A.A. Yaroshevskii, S.V. Bolikhovskaya, E.V. Koptev-Dvornikov, 2006, published in Geokhimiya, 2006, No. 10, pp. 1027–1039.     

Thermal and redox state of the subcontinental lithospheric mantle of NE Spain from thermobarometric data on mantle xenoliths

Mantle xenoliths in within-plate Cenozoic alkaline mafic lavas from NE Spain are used to assess the local subcontinental lithospheric mantle geotherm and the influence of melting and metasomatism on its oxidation state. The xenoliths are mainly anhydrous spinel lherzolites and harzburgites and gradations between, with minor pyroxenites. Most types show protogranular textures, but transitional protogranular–porphyroclastic and equigranular lherzolites also exist. Different thermometers used in the estimates provide higher subsolidus equilibrium temperatures for harzburgites (1,062 ± 29°C) than for lherzolites (972 ± 89°C), although there is overlap; the lowest temperatures correspond to porphyroclastic lherzolites, whereas pyroxenites give the highest temperatures (up to 1,257°C). Maximum pressures for subsolidus equilibrium of peridotites are at 2.0–1.8 GPa. Later they followed adiabatic decompression and harzburgites registered lower pressures (1.02 ± 0.19 GPa) than lherzolites (1.41 ± 0.27 GPa). One pyroxenite gives values consistent with the spinel lherzolite field (1.08 GPa). The shallowest barometric data are in agreement with the highest local conductive geotherms, which implies that the lithosphere–asthenosphere boundary is at 70–60 km minimum depth. Higher equilibrium temperatures for the harzburgites could be explained by the existence of mafic magma bodies or dykes at the lower crust–mantle boundary. Paleo-fO₂ conditions during partial melting as inferred from the covariation between V and MgO concentrations are mainly between QFM−1 and QFM−2 in log units. However, most thermobarometric fO₂ estimates are between QFM−1 and QFM+1, suggesting oxidation caused by later metasomatism during uplift and cooling.     

Trace element variations in olivine phenocrysts from Ugandan potassic rocks as clues to the chemical characteristics of parental magmas

Olivine phenocrysts in ugandite and leucite basanite from the western branch of the East African Rift have been analysed for up to 34 trace elements by Laser-ICP-MS with detection limits as low as 1 ppb. A combination of point analyses with varying ablation crater diameters and line scans allow the identification of subtle zonations from core to rim, as well as characterization of the chemical effects of contamination along cracks. Trace element concentrations are remarkably uniform between large and small phenocrysts; fractionated leucite basanites (Mg# 59) have higher D _Ca and D _Al, and less fractionated LREE/HREE than MgO-rich ugandites (Mg# 75–80). Minor zonation is seen in elements with cation charges from 5+ to 2+ (P, Ti, Zr, Cr, Al, Sc, V, Cu, Mn, Ni) and show correlation between Ti and Al, but not P. Early phenocryst cores with high Li or Ni, low Mn, or enrichments in many trace elements can be identified, whereas xenocrysts have exceptionally low Na, Cr, Ti, V and Co. Partition coefficients for Ni are 31–35, less than in lamproites, with which they demonstrate an approximately linear correlation with K₂O content, K₂O/Al₂O₃ and K₂O/Na₂O of the melt, but none with SiO₂ content or Mg#. D-values for Cr, Mn and Co overlap with those of basalts, whereas those for Sc (0.011–0.018), Zn (0.44–0.49) and Ga (0.006–0.007) are lower. D _V of various potassic rocks (0.015 in the Ugandan rocks) confirms the dependence on fO₂ calibrated by the Fe³⁺/(Fe³⁺+Fe²⁺) of spinels; the Ugandan potassic rocks crystallized at fO₂ = FMQ to FMQ + 1. The ugandite olivines have some trace element characteristics reminiscent of those in metasomatized Kaapvaal peridotites, but not ocean islands. Line scan analyses are contaminated in Al, Ca, Cu, Ga, Sr, Zr, Nb, La and Ce, elements that are also concentrated in microcracks between subgrains, indicating smearing out during polishing, and demonstrating that large spot analyses produce the best results.     

Petrogenetic and geotectonic significance of Neoproterozoic suprasubduction mantle as revealed by the Wizer ophiolite complex,Central Eastern Desert,Egypt

Ophiolite complexes, formed in a suprasubduction zone environment during Neoproterozoic time, are widely distributed in the Eastern Desert of Egypt. Their mantle sections provide important information on the origin and tectonic history of ocean basins these complexes represent. The geochemistry and mineralogy of the mantle section of the Wizer ophiolite complex, represented by serpentinites after harzburgite containing minor dunite bodies, are presented. Presence of antigorite together with the incipient alteration of chromite and absence of chlorite suggests that serpentinization occurred in the mantle wedge above a Neoproterozoic subduction zone. Wizer peridotites have a wide range of spinel compositions. Spinel Cr# [100Cr/(Cr + Al)] decrease gradually from dunite bodies (Cr# = 81–87) and their host highly depleted harzburgites (Cr# = 67–79) to the less depleted harzburgites (Cr# = 57–63). Such decreases in mantle refractory character are accompanied by higher Al and Ti contents in bulk compositions. Estimated parental melt compositions point to an equilibration with melts of boninitic composition for the dunite bodies (TiO₂ = ~<0.07–0.22 wt%; Al₂O₃ = 9.4–10.6 wt%), boninitic-arc tholeiite for the highly depleted harzburgites (TiO₂ = <0.09–0.28 wt%; Al₂O₃ = 11.2–14.1 wt%) and more MORB-like affinities for the less depleted harzburgites (TiO₂ = ~<0.38–0.51 wt%; Al₂O₃ = 14.5–15.3 wt%). Estimated equilibrium melts are found in the overlying volcanic sequence, which shows a transitional MORB–island arc geochemical signature with a few boninitic samples. Enrichment of some chromites in TiO₂ and identification of sulfides in highly depleted peridotites imply interaction with an impregnating melt. A two-stage partial melting/melt–rock reaction model is advocated, whereby, melting of a depleted mantle source by reaction with MORB-like melts is followed by a second stage melting by interaction with melts of IAT–boninitic affinities in a suprasubduction zone environment to generate the highly depleted harzburgites and dunite bodies. The shift from MORB to island arc/boninitic affinities within the mantle lithosphere of the Wizer ophiolite sequence suggests generation in a protoarc-forearc environment. This, together with the systematic latitudinal change in composition of ophiolitic lavas in the Central Eastern Desert (CED) of Egypt from IAT–boninitic affinities to more MORB-like signature, implies that the CED could represent a disrupted forearc-arc-backarc system above a southeast-dipping subduction zone.     

Early Cambrian oceanic plagiogranite in the Silvretta Nappe,eastern Alps: geochemical,zircon U-Pb and Rb-Sr data from garnet-hornblende-plagioclase gneisses

 Garnet–hornblende–plagioclase gneisses rich in incompatible elements occur in the crystalline basement of the Austro-Alpine Silvretta nappe and are associated with clinopyroxene norites and harzburgite cumulates. It is proposed here that the gneisses were formerly oceanic plagiogranites. An ε_{Nd( 530 )} value of +5.6 for the gneisses as well as initial ⁸⁷Sr/⁸⁶Sr values of 0.7036–0.7037 for the gabbroic rocks and 0.7026–0.7027 for the ultramafic rocks suggest a mantle source for this rock association. The geochemical characteristics of the garnet–hornblende–plagioclase gneisses indicate that their precursors were derived by fractional crystallization from a basaltic parent magma, by the same process which produced the adjacent clinopyroxene norites and ultramafic cumulates as well. The combined U–Pb upper intercept ages of zircons from two gneiss samples yield an igneous crystallization age of 532±30 Ma, similar to previously dated (mostly calc-alkaline) orthogneisses in the same area. High-quality transparent zircons showed the least degree of discordance, but contain extremely low U and Pb levels. The rock suite, including this plagiogranite, was emplaced within oceanic crust which formed in the latest Precambrian–early Palaeozoic off the northern continental margin of Gondwana. Received: 26 April 1996 / Accepted: 2 August 1996