Preliminary geochemical study of volcanic rocks in the Pang Mayao area, Phrao, Chiang Mai, northern Thailand: tectonic setting of formation

The least-altered, Permian mafic volcanic rocks from the Pang Mayao area, Phrao District, Chiang Mai Province, part of Chiang Rai–Chiang Mai volcanic belt, have been analyzed and are found to be mid-ocean ridge and ocean–island basalts. The mid-ocean ridge basalts occur as lava flows or dike rocks. They are equigranular, fine- to medium-grained and consist largely of plagioclase, clinopyroxene and olivine. These basalt samples are tholeiitic, and have compositions very similar to T-MORB from the region where the Du Toit Fracture Zone intersects the Southwest Indian Ridge. The ocean–island basalt occurs as pillow breccia, and lava flows or dike rocks. They are slightly to moderately porphyritic, with phenocrysts/microphenocrysts of clinopyroxene, olivine, plagioclase and/or Fe–Ti oxide. The groundmass is very fine-grained, and made up largely of felty plagioclase laths with subordinate clinopyroxene. These basalt samples are alkalic, and chemically analogous to those from Haleakala Volcano, Maui, Hawaiian Chain. These mafic volcanic rocks may have been formed in a major ocean basin rather than in a mature back-arc basin.     

Petrology and geochemistry of Tertiary volcanic rocks from the İkizce (Ordu) area, NE Turkey: Implications for the evolution of the eastern Pontide paleo-magmatic arc

Tertiary volcanism in the İkizce region at the western edge of the eastern Pontides paleo-magmatic arc is represented by basaltic and andesitic rocks associated with sediments deposited in a shallow basin environment. The basaltic rocks contain plagioclase (An_58–80), olivine (Fo_82–84), clinopyroxene (Wo_44–48En_35–42Fs_7–17), hornblende (Mg# = 0.68–0.76) phenocrysts, and magnetite microcrysts, whereas the andesitic rocks include plagioclase (An_25–61), clinopyroxene (Wo_46–49En_38–43Fs_11–13), hornblende (Mg# = 0.48–0.81), biotite (Mg# = 0.48–0.60) phenocrysts, titanomagnetite, apatite, and zircon microcrysts.Geochemical data indicate magmatic evolution from tholeiitic-alkaline transitional to calc-alkaline characteristics with medium-K contents. The geochemical variation in the rocks can be explained by fractionation of common mineral phases such as clinopyroxene, olivine, hornblende, plagioclase, magnetite, and apatite. The trace elements’ distributions of the volcanic rocks show similarities to those of E-Type MORB, have a shape that is typical of rocks from subduction-related tectonic setting with enrichment in LILE and to a lesser extent in LREE, but depletion in HFSE. The rocks evolved from a parental magma derived from an enriched source formed by subduction induced metasomatism of basaltic rocks, the latter formed through clinopyroxene ± olivine controlled fractionation in a high level magma chamber. The andesitic rocks developed through hornblende ± plagioclase controlled fractionation in shallow level magma chamber(s).     

Anhydrous P-T phase relations of near-primary high-alumina basalt from the South Sandwich Islands

Anhydrous P-T phase relations, including phase compositions and modes, are reported from 10–31 kbar for a near-primary high-alumina basalt from the South Sandwich Islands in the Scotia Arc. The water content of natural subduction-related basalt is probably <0.5 wt.% and thus, these results are relevant to the generation of primary basaltic magmas in subduction zones. At high pressures (>27 kbar) garnet is the liquidus phase followed by clinopyroxene, then quartz/coesite at lower temperatures. At intermediate pressures (17–27 kbar), clinopyroxene is the liquidus phase followed by either garnet, quartz, plagioclase, then orthopyroxene or plagioclase, quartz, garnet, then orthopyroxene depending on the pressure within this interval. At all lower pressures, plagioclase is the liquidus phase followed at much lower temperatures (100° C at 5 kbar) by clinopyroxene. The absence of olivine from the liquidus suggests that the composition studied here could not have been derived from a more mafic parent by olivine fractionation at any pressure investigated, and supports the interpretation that it is primary. If so, these results also preclude an origin for this melt by partial melting of olivine-rich mantle periddotite and suggest instead that it was generated by partial melting of the descending slab (quartz eclogite) leaving clinopyroxene, garnet, or both in the residue. The generally flat REE patterns for low-K series subduction related basalts argue against any significant role for garnet, however, and it is thus concluded that the composition studied here was extracted at 20–27 kbar after sufficiently high degrees of partial melting (50%) to totally consume garnet in the eclogite source. Melting experiments on three MORB composition, although not conclusive, are in agreement with this mechanism. Results at 30 kbar support an origin for tonalite/trondhjemite series rocks by lower degrees of melting (15–30%), leaving both garnet and clinopyroxene in the residue.     

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

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

The Petrology of the Tholeiites through Melilite Nephelinites on Gran Canaria, Canary Islands: Crystal Fractionation, Accumulation, and Depths of Melting

We report major and trace element X-ray fluorescence (XRF) datafor mafic volcanics covering the 15-Ma evolution of Gran Canaria,Canary Islands. The Miocene (12–15 Ma) and Pliocene-Quaternary(0–6 Ma) mafic volcanics on Gran Canaria include picrites,tholeiites, alkali basalts, basanites, nephelinites, and melilitenephelinites. Olivineclinopyroxene are the major fractionatingor accumulating phases in the basalts. Plagioclase, Fe–Tioxide, and apatite fractionation or accumulation may play aminor role in the derivation of the most evolved mafic volcanics.The crystallization of clinopyroxene after olivine and the absenceof phenocrystic plagioclase in the Miocene tholeiites and inthe Pliocene and Quaternary alkali basalts and basanites withMgO>6 suggests that fractionation occurred at moderate pressure,probably within the upper mantle. The presence of plagioclasephenocrysts and chemical evidence for plagioclase fractionationin the Miocene basalts with MgO<6 and in the Pliocene tholeiitesis consistent with cooling and fractionation at shallow depth,probably during storage in lower-crustal reservoirs. Magma generationat pressures in excess of 3•0–3•5 GPa is suggestedby (a) the inferred presence of residual garnet and phlogopiteand (b) comparison of FeO¹ cation mole percentages and the CIPWnormative compositions of the mafic volcanics with results fromhigh-pressure melting experiments. The Gran Canaria mafic magmaswere probably formed by decompression melting in an upwellingcolumn of asthenospheric material, which encountered a mechanicalboundary layer at {small tilde}100-km depth.     

Superposition of replacements in the mafic granulites of the Jijal complex of the Kohistan arc, northern Pakistan: dehydration and rehydration within deep arc crust

A deep-level crustal section of the Cretaceous Kohistan arc is exposed in the northern part of the Jijal complex. The occurrence of mafic to ultramafic granulite-facies rocks exhibits the nature and metamorphic evolution of the lower crust. Mafic granulites are divided into two rock types: two-pyroxene granulite (orthopyroxene+clinopyroxene+plagioclase±quartz [1]); and garnet–clinopyroxene granulite (garnet+clinopyroxene+plagioclase+quartz [2]). Two-pyroxene granulite occurs in the northeastern part of the Jijal complex as a relict host rock of garnet–clinopyroxene granulite, where the orthopyroxene-rich host is transected by elongated patches and bands of garnet–clinopyroxene granulite. Garnet–clinopyroxene granulite, together with two-pyroxene granulite, has been partly replaced by amphibolite (hornblende±garnet+plagioclase+quartz [3]). The garnet-bearing assemblage [2] is expressed by a compression–dehydration reaction: hornblende+orthopyroxene+plagioclase=garnet+clinopyroxene+quartz+H₂O↑. Subsequent amphibolitization to form the assemblage [3] is expressed by two hydration reactions: garnet+clinopyroxene+plagioclase+H₂O=hornblende+quartz and plagioclase+hornblende+H₂O=zoisite+chlorite+quartz. The mafic granulites include pod- and lens-shaped bodies of ultramafic granulites which consist of garnet hornblendite (garnet+hornblende+clinopyroxene [4]) associated with garnet clinopyroxenite, garnetite, and hornblendite. Field relation and comparisons in modal–chemical compositions between the mafic and ultramafic granulites indicate that the ultramafic granulites were originally intrusive rocks which dissected the protoliths of the mafic granulites and then have been metamorphosed simultaneously with the formation of garnet–clinopyroxene granulite. The results combined with isotopic ages reported elsewhere give the following tectonic constraints: (1) crustal thickening through the development of the Kohistan arc and the subsequent Kohistan–Asia collision caused the high-pressure granulite-facies metamorphism in the Jijal complex; (2) local amphibolitization of the mafic granulites occurred after the collision.     

The petrogenesis of the Kangâmiut dyke swarm,W. Greenland

Previous studies have shown that the 2.04 Ga Kangâmiut dyke swarm of SW Greenland was injected into an active tectonic environment associated with the formation of the Nagssugtoqidian orogenic belt. Major and trace element modelling of the swarm shows that its chemical evolution was controlled by simple clinopyroxene–plagioclase fractionation. However, such trends — although typical of continental flood basalts and mafic dyke swarms — are at variance with their mineralogy and petrography, which show that locally hornblende is the dominant primary ferromagnesian mineral. Modelling of intradyke fractionation alone shows that hornblende could locally have been an important crystallising phase within several dykes. Normal basaltic fractionation must have occurred before dyke injection at the exposed crustal levels, where the influx of water into the dykes is believed to be responsible for the transition from clinopyroxene–plagioclase (tholeiitic) to hornblende–plagioclase±oxides (calc–alkaline) crystallisation. Overall geochemical trends are dominated by tholeiitic fractionation because (1) hornblende fractionation tended to buffer chemical composition; (2) the presence of water in the surrounding country rocks may have resulted in the advection of heat away from the dyke and consequently resulted in rapid crystallisation, particularly in thin dykes. There is no evidence from trace element data, and particularly Pb isotopic ratios, of any significant assimilation of country rocks occurring during clinopyroxene–plagioclase fractionation, although this does not preclude contamination of the mantle source prior to magma generation. It is likely that the incompatible element enrichment within the dykes resulted from subduction-related mantle metasomatism. The Kangâmiut dyke swarm was both a syn-tectonic and thermal event, which triggered it may be linked to passage of a slab window underneath the metasomatised region, or a mantle plume ascending under a subduction zone.     

Commingling and mixing of S-type peraluminous, ultrapotassic and basaltic magmas in the Cayconi volcanic field, Cordillera de Carabaya, SE Peru

The Cayconi district of the Cordillera de Carabaya, SE Peru, exposes a remnant of an upper Oligocene–Lower Miocene (22.2–24.4 Ma) volcanic field, comprising a diverse assemblage of S-type silicic and calc-alkaline basaltic to andesitic flows, members of the Picotani Group of the Central Andean Inner Arc. Basaltic flows containing olivine, plagioclase, clinopyroxene, ilmenite and glass, and glassy rhyolitic agglutinates with phenocrystic quartz, cordierite, plagioclase, sanidine, ilmenite and apatite, respectively exhibit mineralogical and geochemical features characteristic of medium-K mafic and Lachlan S-type silicic lavas. Cordierite-bearing dacitic agglomerates and lavas, however, are characterized by dispersed, melanocratic micro-enclaves and phenocrysts set in a fine-grained quartzo-feldspathic matrix. They contain a bimodal mica population, comprising phlogopite and biotite, as well as complexly zoned, sieve-textured plagioclase grains, sector-zoned cordierite, sanidine, quartz, irregular patches of replaced olivine, clinopyroxene and orthopyroxene and accessory phases including zircon, monazite, ilmenite and chromite. The coexistence of minerals not in mutual equilibrium and the growth/dissolution textures exhibited by plagioclase are features indicative of magmatic commingling and mixing. Trachytic-textured andesite flows interlayered with olivine+plagioclase–glomerophyric, calc-alkaline basalts have a phenocrystic assemblage of resorbed orthopyroxene and plagioclase and exhibit melanocratic groundmass patches of microphenocrystic phlogopite, Ca-rich sanidine, ilmenite and aluminous spinel. The mineralogical and mineral chemical relationships in both the dacites and the trachytic-textured andesites imply subvolcanic mixing between distinct ultrapotassic mafic melts, not represented by exposed rock types, and both the S-type silicic and calc-alkaline mafic magmas. Such mixing relationships are commonly observed in the Oligo-Miocene rocks of the Cordillera de Carabaya, suggesting that the S-type rocks in this area and, by extension, elsewhere derive their unusually high K₂O, Ba, Sr, Cr and Ni concentrations from commingling and mixing with diverse, mantle-derived potassic mafic magmas.     

Chemical constraints on the petrogenesis of mildly alkaline lavas from Vestmannaeyjar,Iceland: the Eldfell (1973) and Surtsey (1963–1967) eruptions

The Vestmannaeyjar archipelago is composed of alkalic lavas erupted at the southern end of the active, southward propagating, Eastern Volcanic Zone. Recent eruptions include the most primitive (Surtsey) and most evolved (Eldfell) compositions found in this area. We studied time-stratigraphic sample suites from both eruptions to characterize the magmatic environment of Vestmannacyjar. All samples are nearly homogeneous in radiogenic isotopic ratios (⁸⁷Sr/⁸⁶Sr 0.70304 to 0.70327;¹⁴³Nd/¹⁴⁴Nd 0.51301 to 0.50307;²⁰⁶Pb/²⁰⁴Pb 18.96 to 19.18;²⁰⁷Pb/²⁰⁴Pb 15.50 to 15.53;²⁰⁸Pb/²⁰⁴Pb 38.47 to 38.76; KH Park and A Zindler, in preparation). Compositional trends of lavas from the two eruptions are not consistent with fractionation in a near-surface environment, but indicate rather moderate pressure evolution of small magma batches. At Eldfell, mugearite lavas can be modeled by 30% closed-system fractional crystallization of olivine+plagioclase+clinopyroxene+Fe–Ti oxides from parental hawaiite. The phase proportions are consistent with an experimentally determined moderate pressure (8 kbar) cotectic in mildly alkaline systems (Mahood and Baker 1986). Compositional variations of Surtsey lavas can be modeled by crystallization of clinopyroxene+olivine+plagioclase+minor Fe–Ti oxides. The presence of sodic plagioclase megacrysts and clinopyroxene with 8 wt% Al₂O₃ in xenoliths from Surtsey lavas are consistent with a moderate pressure fractionation event. Based on major-element and REE data the most primitive Surtsey lavas formed by small degrees of melting of a lherzolite source. The alkaline nature of Vestmannaeyjar lavas is not the result of assimilation of lower crustal melts (cf. Oskarsson et al. 1985; Steinthorsson et al. 1985).     

Petrology and geochemistry of the Huerto Andesite,San Juan volcanic field,Colorado

The Huerto Andesite is the largest of several andesite sequences interlayered with the large-volume ash-flow tuffs of the San Juan volcanic field, Colorado. Stratigraphically this andesite is between the region's largest tuff (the 27.8 Ma, 3,000 km³ Fish Canyon Tuff) and the evolved product of the Fish Canyon Tuff (the 27.4 Ma, 1,000 km³ Carpenter Ridge Tuff), and eruption was from vents located approximately 20–30 km southwest and southeast of calderas associated with these ashflow tuffs. Olivine phenocrysts are present in the more mafic, SiO₂-poor samples of andesite, hence the parent magma was most likely a mantle-derived basaltic magma. The bulk compositions of the olivine-bearing andesites compared to those containing orthopyroxene phenocrysts suggest the phenocryst assemblage equilibrated at 2–5 kbar. Two-pyroxene geothermometry yields equilibrium temperatures consistent with near-peritectic magmas at 2–5 kbar. Fractionation of phenocryst phases (olivine or orthopyroxene + clinopyroxene + plagioclase + Ti-magnetite + apatite) can explain most major and trace element variations of the andesites, although assimilation of some crustal material may explain abundances of some highly incompatible trace elements (Rb, Ba, Nb, Ta, Zr, Hf) in the most evolved lavas. Despite the great distance of the San Juan volcanic field from the inferred Oligocene destructive margin, the Huerto Andesite is similar to typical plate-margin andesites: both have relatively low abundances of Nb and Ta and similar values for trace-element ratios such as La/Yb and La/Nb.Deriving the Fish Canyon and Carpenter Ridge Tuffs by crystal fractionation from the Huerto Andesite cannot be dismissed by major-element models, although limited trace-element data indicate the tuffs may not have been derived by such direct evolution. Alternatively, heat of crystallization released as basaltic magmas evolved to andesitic compositions may have caused melting of crust to produce the felsic-ash flows. Mafic magmas may have been gravitationally trapped below lighter felsic magmas; mafic magmas which ascended to the surface probably migrated upwards around the margins of silicic chambers, as suggested by the present-day outcrops of andesitic units around the margins of recognized ash-flow calderas.     

Migration and accumulation of ultra-depleted subduction-related melts in the Massif du Sud ophiolite (New Caledonia)

The Massif du Sud is a large ophiolitic complex that crops out in the southern region of New Caledonia (SW Pacific). It is dominated by harzburgite tectonite that locally shows a transitional gradation to massive dunite up section. Clinopyroxene, orthopyroxene and plagioclase progressively appear in dunite up to the transition to layered wehrlite and orthopyroxene–gabbro. The dunite–wehrlite and wehrlite–gabbro contacts are parallel and the latter defines the paleo-Moho.Highly depleted modal, mineral and bulk rock compositions indicate that harzburgites are residues after high degrees (20–30%) of partial melting mainly in the spinel-stability field. Their relative enrichment in HFSE, LREE and MREE is due to re-equilibration of melting residues with percolating melts. Dunite formed in the Moho transition zone by reaction between residual mantle harzburgite and olivine-saturated melts that led to pyroxene dissolution and olivine precipitation. Rare clinopyroxene and plagioclase crystallized in interstitial melt pores of dunite from primitive, low-TiO₂, ultra-depleted liquids with a geochemical signature transitional between those of island arc tholeiites and boninites.Ascending batches of relatively high-SiO₂, ultra-depleted melts migrated through the Moho transition zone and generated wehrlite by olivine dissolution and crystallization of clinopyroxene, orthopyroxene and plagioclase in variable amounts. These liquids were more evolved and were produced by higher degrees of melting or from a more depleted source compared with melts that locally crystallized clinopyroxene in dunite. Ultra-depleted magmas, non-cogenetic with those that formed the Moho transition zone, ascended to the lower crust and generated gabbroic cumulates with subduction-related affinity. Thus, the ultramafic and mafic rocks in the Moho transition zone and lower crust of the Massif du Sud ophiolite are not products of fractional crystallization from a single magma-type but are the result of migration and accumulation of different melts in a multi-stage evolution.The record of high partial melting in the mantle section, and migration and accumulation of ultra-depleted subduction-related melts in the Moho transition zone and lower crust support that the Massif du Sud ophiolite is a portion of forearc lithosphere generated in an extensional regime during the early phases of the subduction zone evolution. Our results show the existence of different types of ultra-depleted melt compositions arriving at the Moho transition zone and lower crust of an infant intraoceanic paleo-arc. Ultra-depleted melts may thus be a significant component of the melt budget generated in oceanic spreading forearcs prior to aggregation and mixing of a large range of melt compositions in the crust.     

Type-II xenoliths and related metasomatism from the Nógrád-Gömör Volcanic Field, Carpathian-Pannonian region (northern Hungary–southern Slovakia)

Xenoliths from the upper mantle and lower crust are abundant in Plio–Pleistocene alkali basalts of the Nógrád-Gömör Volcanic Field (NGVF; northern Pannonian Basin, northern Hungary/southern Slovakia), representing a valuable ‘probe’ of lithospheric structures and processes. Ultramafic xenoliths have been divided into two groups: (1) Type-I, composed mostly of olivine with subsidiary orthopyroxene, clinopyroxene and spinel, and (2) Type-II, containing mostly Al- and Ti-rich clinopyroxene with subordinate olivine, spinel and plagioclase. Both types often contain amphibole and, to a lesser extent, mica. The refractory character of Type-I xenoliths suggests they represent mantle depleted by prior episodes of partial melting. In contrast, Type-II series (wehrlites, olivine clinopyroxenites, clinopyroxenites and plagioclase-bearing ultramafic lithologies), on the basis of their textural features, thermobarometric histories and major and trace element variation, appear to have formed as magmatic cumulates. Petrologic and geochemical studies of Type-II xenoliths from Nógrád-Gömör suggest they crystallized from basaltic melts emplaced within the lithospheric mantle and lower crust, prior to the onset of Plio–Pleistocene volcanic activity. After their consolidation, metasomatic agents reacted with the anhydrous cumulate phases producing amphiboles and micas at the expense of olivine and clinopyroxene. The metasomatic agents appear to have been adakitic rather than basaltic in composition, possibly linked to a retreating arc–forearc system. Large-scale contamination of the lithospheric mantle can therefore be attributed to fluid and melt fractions related to subduction beneath the outer Carpathian arc.     

Inter-mineral Fe isotope variations in mantle-derived rocks and implications for the Fe geochemical cycle

Iron isotope and major- and minor-element compositions of coexisting olivine, clinopyroxene, and orthopyroxene from eight spinel peridotite mantle xenoliths; olivine, magnetite, amphibole, and biotite from four andesitic volcanic rocks; and garnet and clinopyroxene from seven garnet peridotite and eclogites have been measured to evaluate if inter-mineral Fe isotope fractionation occurs in high-temperature igneous and metamorphic minerals and if isotopic fractionation is related to equilibrium Fe isotope partitioning or a result of open-system behavior. There is no measurable fractionation between silicate minerals and magnetite in andesitic volcanic rocks, nor between olivine and orthopyroxene in spinel peridotite mantle xenoliths. There are some inter-mineral differences (up to 0.2‰ in ⁵⁶Fe/⁵⁴Fe) in the Fe isotope composition of coexisting olivine and clinopyroxene in spinel peridotites. The Fe isotope fractionation observed between clinopyroxene and olivine appears to be a result of open-system behavior based on a positive correlation between the Δ⁵⁶Fe_{clinopyroxene-olivine} fractionation and the δ⁵⁶Fe value of clinopyroxene and olivine. There is also a significant difference in the isotopic compositions of garnet and clinopyroxene in garnet peridotites and eclogites, where the average Δ⁵⁶Fe_{clinopyroxene-garnet} fractionation is +0.32 ± 0.07‰ for six of the seven samples. The one sample that has a lower Δ⁵⁶Fe_{clinopyroxene-garnet} fractionation of 0.08‰ has a low Ca content in garnet, which may reflect some crystal chemical control on Fe isotope fractionation. The Fe isotope variability in mantle-derived minerals is interpreted to reflect subduction of isotopically variable oceanic crust, followed by transport through metasomatic fluids. Isotopic variability in the mantle might also occur during crystal fractionation of basaltic magmas within the mantle if garnet is a liquidus phase. The isotopic variations in the mantle are apparently homogenized during melting processes, producing homogenous Fe isotope compositions during crust formation.     

Melts of garnet lherzolite: experiments, models and comparison to melts of pyroxenite and carbonated lherzolite

Phase equilibrium experiments on a compositionally modified olivine leucitite from the Tibetan plateau have been carried out from 2.2 to 2.8 GPa and 1,380–1,480 °C. The experiments-produced liquids multiply saturated with spinel and garnet lherzolite phase assemblages (olivine, orthopyroxene, clinopyroxene and spinel ± garnet) under nominally anhydrous conditions. These SiO₂-undersaturated liquids and published experimental data are utilized to develop a predictive model for garnet lherzolite melting of compositionally variable mantle under anhydrous conditions over the pressure range of 1.9–6 GPa. The model estimates the major element compositions of garnet-saturated melts for a range of mantle lherzolite compositions and predicts the conditions of the spinel to garnet lherzolite phase transition for natural peridotite compositions at above-solidus temperatures and pressures. We compare our predicted garnet lherzolite melts to those of pyroxenite and carbonated lherzolite and develop criteria for distinguishing among melts of these different source types. We also use the model in conjunction with a published predictive model for plagioclase and spinel lherzolite to characterize the differences in major element composition for melts in the plagioclase, spinel and garnet facies and develop tests to distinguish between melts of these three lherzolite facies based on major elements. The model is applied to understand the source materials and conditions of melting for high-K lavas erupted in the Tibetan plateau, basanite–nephelinite lavas erupted early in the evolution of Kilauea volcano, Hawaii, as well as younger tholeiitic to alkali lavas from Kilauea.     

Melting and phase relations in the plane tholeiite-lherzolite-nepheline basanite to 40 kilobars with geological implications

Six crystalline mixtures, picrite, olivine-rich tholeiite, nepheline basanite, alkali picrite, olivine-rich basanite, and olivine-rich alkali basalt were recrystallized at pressures to 40 kb, and the phase equilibria and sequences of phases in natural basaltic and peridotitic rocks were investigated.The picrite was recrystallized along the solidus to the assemblages (1) olivine+orthopyroxene+ clinopyroxene +plagioclase+spinel below 13 kb, (2) olivine+orthopyroxene+clinopyroxene+spinel between 13 kb and 18 kb, (3) olivine+orthopyroxene+clinopyroxene+ garnet+spinel between 18 kb and 26 kb, and (4) olivine+clinopyroxene+garnet above 26 kb. The solidus temperature at 1 atm is slightly below 1,100° and rises to 1,320° at 20 kb and 1,570° at 40 kb. Olivine is the primary phase crystallizing from the melt at all pressures to 40 kb.The olivine-rich tholeiite was recrystallized along the solidus into the assemblages (1) olivine+ clinopyroxene+plagioclase+spinel below 13 kb, (2) clinopyroxene+orthopyroxene+ spinel between 13 kb and 18 kb, (3) clinopyroxene+garnet+spinel above 18 kb. The solidus temperature is slightly below 1,100° at 1 atm, 1,370° at 20 kb, and 1,590° at 40 kb. The primary phase is olivine below 20 kb but is orthopyroxene at 40 kb.In the nepheline basanite, olivine is the primary phase below 14 kb, but clinopyroxene is the first phase to appear above 14 kb. In the alkali-picrite the primary phase is olivine to 40 kb. In the olivine-rich basanite, olivine is the primary phase below 35 kb and garnet is the primary phase above 35 kb. In the olivine-rich alkali basalt the primary phase is olivine below 20 kb and is garnet at 40 kb.Mineral assemblages in a granite-basalt-peridotite join are summarized according to reported experimental data on natural rocks. The solidus of mafic rock is approximately given by T=12.5 P _Kb+1,050°. With increasing pressure along the solidus, olivine disappears by reaction with plagioclase at 9 kb in mafic rocks and plagioclase disappears by reaction with olivine at 13 kb in ultramafic rocks. Plagioclase disappears at around 22 kb in mafic rocks, but it persists to higher pressure in acidic rocks. Garnet appears at somewhat above 18 kb in acidic rocks, at 17 kb in mafic rocks, and at 22 kb in ultramafic rocks.The subsolidus equilibrium curves of the reactions are extrapolated according to equilibrium curves of related reactions in simple systems. The pyroxene-hornfels and sanidinite facies is the lowest pressure mineral facies. The pyroxene-granulite facies is an intermediate low pressure mineral facies in which olivine and plagioclase are incompatible and garnet is absent in mafic rocks. The low pressure boundary is at 7.5 kb at 750° C and at 9.5 kb at 1,150° C. The high pressure boundary is 8.0 kb at 750° C and 15.0 kb at 1,150° C. The garnet-granulite facies is an intermediate high pressure facies and is characterized by coexisting garnet and plagioclase in mafic rocks. The upper boundary is at 10.3 kb at 750° C and 18.0 kb at 1,150° C. The eclogite facies is the highest pressure mineral facies, in which jadeite-rich clinopyroxene is stable.Compositions of minerals in natural rocks of the granulite facies and the eclogite facies are considered. Clinopyroxenes in the granulite-facies rocks have smaller jadeite-Tschermak's molecule ratios and higher amounts of Tschermak's molecule than clinopyroxenes in the eclogite-facies rocks. The distribution coefficients of Mg between orthopyroxene and clinopyroxene are normally in the range of 0.5–0.6 in metamorphic rocks in the granulite facies. The distribution coefficients of Mg between garnet and clinopyroxene suggest increasing crystallization temperature of the rocks in the following order: eclogite in glaucophane schist, eclogite and granulite in gneissic terrain, garnet peridotite, and peridotite nodules in kimberlite.Temperatures near the bottom of the crust in orogenic zones characterized by kyanitesillimanite metamorpbism are estimated from the mineral assemblages of metamorphic rocks in Precambrian shields to be about 700° C at 7 kb and 800° C at 9 kb, although heat-flow data suggest that the bottom of Precambrian shield areas is about 400° C and the eclogite facies is stable.The composition of liquid which is in equilibrium with peridotite is estimated to be close to tholeiite basalt at the surface pressure and to be picrite at around 30 kb. The liquid composition becomes poorer in normative olivine with decreasing pressure and temperature.During crystallization at high pressure, olivine and orthopyroxene react with liquid to form clinopyroxene, and a discontinuous reaction series, olivine orthopyroxene clinopyroxene is suggested. By fractional crystallization of pyroxenes the liquid will become poorer in SiO₂. Therefore, if liquid formed by partial melting of peridotite in the mantle slowly rises maintaining equilibrium with the surrounding peridotite, the liquid will become poorer in MgO by crystallization of olivine, and tholeiite basalt magma will arrive at the surface. On the other hand, if the liquid undergoes fractional crystallization in the mantle, the liquid may change in composition to alkali-basalt magma and alkali-basalt volcanism may be seen at a late stage of volcanic activity.Publication No. 681, Institute of Geophysics and Planetary Physics, University of California, Los Angeles.     

Subduction-related Jurassic andesites in the northern Great Caucasus

During the Jurassic the major tectonic units of the Great Caucasus (Bechasyn, Front Range, Main Range and Southern Slope zone) were affected by intensive magmatic activity. Magmatism within the Bechasyn zone, the northernmost unit, which represents the southern part of the Variscan-consolidated Skythian platform is considered here. With the beginning of the Early Jurassic this zone was reactivated by subsidence, accompanied by the deposition of epicontinental shallow water sediments. The Lower Jurassic portion of this sedimentary pile was intruded by numerous sills which display a clear temporal and spatial evolution. The older basic rocks are lower in the profile than the younger, more acidic rocks. A set of 75 samples, representing all exposed sills and their feeder-dikes, was analyzed for major and 21 trace elements. All samples appear more or less affected by alteration under lower greenschist facies conditions. However, these alterations essentially took place on local scales and did not affect the overall chemistry. According to their main element composition the rocks constitute a calc-alkaline series ranging from basaltic—andesitic to rhyolitic. Most of the samples are andesites. Chemically, these andesites closely resemble modern orogenic andesites occurring at convergent plate margins. Altogether, the field evidence and the chemical and mineralogical data obtained show the investigated rocks to be comagmatic and derived from basalt—andesitic initial melts by magmatic fractionation processes. Tholeiitic melts have to be considered as parental magmas, which according to the trace element characteristics of the basalt-andesitic rocks, were generated from an enriched peridotitic mantle source. ⁸⁷Sr/⁸⁶Sr isotope ratios and ¹⁸O values confirm the mantle origin of this rock series. The observed compositional evolution can be explained as a result of olivine and clinopyroxene fractionation of the tholeitic melts followed by amphibole and plagioclase separation. ⁴⁰Ar/³⁹Ar measurements on biotite and plagioclase phenocrysts separated from these rocks vary between 190 and 180 Ma and thereby place the magmatic activity in the late Early Jurassic, in good agreement with the stratigraphic observations. Genetically, the calc-alkaline rocks are related to a subduction zone of the Andean type. Their chemical and isotopic compositions and their age setting corroborate the plate tectonic models for the evolution of the Caucasus orogenic belt during the Jurassic.Dedicated to the late A. M. Borsuk, initiator of the study     

Geochemistry,petrogenesis and tectonic significance of the basic volcanic units of the Zildat ophiolitic mélange,Indus suture zone,eastern Ladakh (India)

Abstract

Basic volcanic rocks within the Zildat ophiolitic mélange of Indus suture zone in eastern Ladakh are medium to fine grained with partially preserved primary texture and mineralogy. These rocks are predominantly alkaline basalt with high Nb/Y and enriched incompatible trace element characteristics, similar to those of the oceanic island basalt (OIB). The minor sub-alkaline basaltic rocks resemble N-type mid ocean ridge basalt (N-MORB) but with much lower abundances of incompatible trace element including REE. The alkaline rocks probably generated through variable, but low degrees of partial melting of enriched mantle source and evolved through high pressure olivine and clinopyroxene fractionation. Low pressure plagioclase and Fe- Ti oxide do not appear to be major fractionating phases. Limited data on the sub-alkaline rocks suggest that their parental melts were derived from mantle sources some what similar to that of N- MORB. Significant role of added cumulates of olivine, clinopyroxene and Fe- Ti oxides is also indicated in their genesis. Ophiolitic mélanges all along the Indus suture zone appear to have formed due to the accumulation of mélange material in the upper part of the subduction zone where they suffered glaucophanitic (blueschist) metamorphism and retrograded partially to greenschist grade as these were subsequently obducted to its present position probably during the Cenozoic Himalayan orogeny due to collision of Indian and Eurasian plates.     

Parental magmas of the Nain Plutonic Suite anorthosites and mafic cumulates: a trace element modelling approach

Equilibrium melt trace element contents are calculated from Proterozoic Nain Plutonic Suite (NPS) mafic and anorthositic cumulates, and from plagioclase and orthopyroxene megacrysts. Assumed trapped melt fractions (TMF) <20% generally eliminate all minor phases in most mafic cumulate rocks, reducing them to mixtures of feldspar, pyroxene and olivine, which would represent the high-temperature cumulus assemblage. In anorthosites, TMF <15% generally reduce the mode to a feldspar-only assemblage. All model melts have trace element profiles enriched in highly incompatible elements relative to normal mid-ocean ridge basalt (NMORB); commonly with negative Nb and Th anomalies. Most mafic cumulates yield similar profiles with constant incompatible element ratios, and can be linked through fractional crystallization. High K-La subtypes probably represent crust-contaminated facies. Mafic cumulates are inferred to belong to a tholeiitic differentiation series, variably contaminated by upper and lower crustal components, and probably related to coeval tholeiitic basaltic dyke swarms and lavas in Labrador. Model melts from anorthosites and megacrysts have normalized trace element profiles with steeper slopes than those calculated from mafic cumulates, indicating that mafic cumulates and anorthosites did not crystallize from the same melts. Orthopyroxene megacrysts yield model melts that are more enriched than typical anorthositic model melts, precluding an origin from parental melts. Jotunites have lower K-Rb-Ba-Y-Yb and higher La-Ce than model residues from fractionation of anorthositic model melts, suggesting they are not cosanguineous with them, but provide reasonable fits to evolved mafic cumulate model melts. Incompatible element profiles of anorthositic model melts closely resemble those of crustal melts such as tonalites, with steep Y-Yb-Lu segments that suggest residual garnet in the source. Inversion models yield protoliths similar to depleted lower crustal granulite xenoliths with aluminous compositions, suggesting that the incompatible trace element budget of the anorthosites are derived from remobilization of the lower crust. The similarity of the highly incompatible trace elements and LILE between anorthositic and mafic cumulate model melts suggests that the basalts parental to the mafic cumulates locally assimilated considerable quantities of the same crust that yielded the anorthosites. The reaction between underplating basalt and aluminous lower crust would have forced crystallization of abundant plagioclase, and remobilization of these hybrid plagioclase-rich mushes then produced the anorthosite massifs.     

Bimodal magmatism of the Tucumã area,Carajás province: U-Pb geochronology,classification and processes

Geological mapping of the Tucumã area has enabled the identification of dike swarms intruded into an Archean basement. The disposition of these dikes is consistent with the well-defined NW-SE trending regional faults, and they can reach up to 20 km in length. They were divided into three main groups: (i) felsic dikes (70% of the dikes), composed exclusively of porphyritic rhyolite with euhedral phenocrysts of quartz and feldspars immersed in an aphyric felsite matrix; (ii) mafic dikes, with restricted occurrence, composed of basaltic andesite and subordinate basalt, with a mineralogical assembly consisting dominantly of plagioclase, clinopyroxene, orthopyroxene and olivine; and (iii) intermediate rocks, represented by andesite and dacite. Dacites are found in outcrops associated with felsic dikes, representing different degrees of hybridization or mixture of mafic and felsic magmas. This is evidenced by a large number of mafic enclaves in the felsic dikes and the frequent presence of embayment textures. SHRIMP U-Pb zircon dating of felsic dikes yielded an age of 1880.9 ± 3.3 Ma. The felsic dikes are peraluminous to slightly metaluminous and akin to A2, ferroan and reduced granites. The intermediate and mafic dikes are metaluminous and belong to the tholeiitic series. Geochemical modeling showed that mafic rocks evolved by pyroxene and plagioclase crystallization, while K-feldspar and biotite are the fractionate phases in felsic magma. A simple binary mixture model was used to determine the origin of intermediate rocks. It indicated that mixing 60% of rhyolite and 40% basaltic andesite melts could have generated the dacitic composition, while the andesite liquid could be produced by mixing of 60% and 40% basaltic andesite and rhyolite melts, respectively. The mixing of basaltic and andesitic magmas probably occurred during ascent and storage in the crust, where andesite dikes are likely produced by a more homogeneous mixture at high depths in the continental crust (mixing), while dacite dikes can be generated in the upper crust at a lower temperature, providing a less efficient mixing process (mingling). The affinities observed between the felsic to intermediate rocks of the Rio Maria and São Felix do Xingu areas and the bimodal magmatism of the Tucumã area reinforce the hypothesis that in the Paleoproterozoic the Carajás province was affected by processes involving thermal perturbations in the upper mantle, mafic underplating, and associated crustal extension or transtension. The 1.88 Ga fissure-controlled A-type magmatism of the Tucumã area was emplaced ∼1.0 to ∼0.65 Ga after stabilization of the Archean crust. Its origin is not related to subduction processes but to the disruption of the supercontinent at the end of the Paleoproterozoic.     

Origin of 1.8 Ga zircons in Post Eocene mafic dikes in the Roshtkhar area,NE Iran

The Roshtkhar area is located in the Khaf-Kashmar-Bardaskan volcano-plutonic belt to the northeastern Iran along the regional E–W trending Dorouneh Fault, northeastern of the Lut Block. There are several outcrops of subvolcanic rocks occurring mainly as dikes in the area, which intruded into Cenozoic intrusive rocks. We present U–Pb dating of zircons from a diabase dike and syenite rock using LA-ICP-MS that yielded an age of 1778 ± 10 Ma for the dike, indicating this Cenozoic dike has zircon xenocrysts inherited from deeper sources; and 38.0 ± 0.5 Ma, indicating an Late Eocene crystallization age for the syenite. Geochemically, the dikes typical of high-K calc-alkaline to shoshonitic magmas. Petrographic observations and major and trace element variations suggest that diabase melts underwent variable fractionation of clinopyroxene, olivine, and Fe-Ti oxides and minor crustal contamination during the differentiation process. Primitive mantle-normalized multi-element diagrams display enrichment in LILE, such as Rb, Ba, Th, U, and Sr compared to HFSE, as well as negative anomalies of Nb, Ta, P, and Ti, suggesting derivation from subduction-modified mantle. Chondrite-normalized REE plots show moderately LREE enriched patterns (<3.83 La_N/Yb_N <8.27), and no significant Eu anomalies. Geochemical modelling using Sm/Yb versus La/Yb and La/Sm ratios suggests a low-degree of batch melting (~1–3%) of a phlogopite-spinel peridotite source to generate the mafic dikes. The geochemical signatures suggest that the Roshtkhar mafic dikes cannot be related directly to subduction and likely resulted from melting of upper mantle in an extensional setting where the heat flow was provided from deeper levels. These dikes presumably derived the zircon xenocrysts from the assimilation of upper crust of Gondwanian basement. Processes responsible for partial melting of metasomatized lithospheric mantle and post-collision magmatism in NE Iran was triggered by heating due to asthenospheric upwelling in an extensional setting.