Inclusions of silicate and sulfate melts in chrome diposide from the Inagli deposit,Yakutia, Russia

Melt inclusions were studied in chrome diopside from the Inagli deposit of gemstones in the Inagli massif of alkaline ultrabasic rocks of potassic affinity in the northwestern Aldan shield, Yakutia, Russia. The chrome diopside is highly transparent and has an intense green color. Its Cr₂O₃ content varies from 0.13 to 0.75 wt %. Primary and primary-secondary polyphase inclusions in chrome diopside are dominated by crystal phases (80–90 vol %) and contain aqueous solution and a gas phase. Using electron microprobe analysis and Raman spectroscopy, the following crystalline phases were identified. Silicate minerals are represented by potassium feldspar, pectolite [NaCa₂Si₃O₈(OH)], and phlogopite. The most abundant minerals in the majority of inclusions are sulfates: glaserite (aphthitalite) [K₃Na(SO₄)₂], glauberite [Na₂Ca(SO₄)₂], aluminum sulfate, anhydrite (CaSO₄), gypsum (CaSO₄ × 2H₂O), barite (BaSO₄), bloedite [Na₂Mg(SO₄)₂ × 4H₂O], thenardite (NaSO₄), polyhalite [K₂Ca₂Mg(SO₄)₄ × 2H₂O], arcanite (K₂SO₄), and celestite (SrSO₄). In addition, apatite was detected in some inclusions. Chlorides are probably present among small crystalline phases, because some analyses of aggregates of silicate and sulfate minerals showed up to 0.19–10.3 wt % Cl. Hydrogen was identified in the gas phase of polyphase inclusions by Raman spectroscopy. The composition of melt from which the chrome diopside crystallized was calculated on the basis of the investigation of silicate melt inclusions. This melt contains 53.5 wt % SiO₂, considerable amounts of CaO (16.3 wt %), K₂O (7.9 wt %), Na₂O (3.5 wt %), and SO₃ (1.4 wt %) and moderate amounts of Al₂O₃ (7.5 wt %), MgO (5.8 wt %), FeO (1.1 wt %), and H₂O (0.75 wt %). The content of Cr₂O₃ in the melt was 0.13 wt %. Many inclusions were homogenized at 770–850°C, when all of the crystals and the gas phase were dissolved. The material of inclusions heated up to the homogenization temperature became heterogeneous even during very fast quenching (two seconds) producing numerous small crystals. This fact implies that most of the inclusions contained a salt (rather than silicate) melt of sulfate-dominated composition. Such inclusions were formed from salt globules (with a density of about 2.5 g/cm³) occurring as an emulsion in the denser (2.6 g/cm³) silicate melt from which the chrome diopside crystallized.     

Early Cretaceous volcanic and sub-volcanic rocks in the Erlian Basin and adjacent areas,Northeast China: new geochemistry,geochronology and zircon Hf isotope constraints on petrogenesis and tectonic setting

ABSTRACT

Early Cretaceous volcanic rocks are widely distributed in northeast China and being extensively observed recently. However, petrogenesis and tectonic setting of these volcanic rocks are still on debate. We present zircon U–Pb ages, whole-rock geochemistry and zircon Hf isotope for these volcanic and sub-volcanic rocks surrounding the Erlian Basin including basic-intermediate volcanic rocks, intermediate-felsic volcanic rocks, and dacites and trachyandesite from dikes. The zircon U–Pb dating results indicate that these rocks formed in the Early Cretaceous (146–129 Ma). The basic-intermediate volcanic rocks mainly consist of basaltic andesite, which are featured by low SiO₂ concentrations (49.96–58.34 wt. %), high Mg^# values (54–37) and Co contents (17.85–25.98 ppm), and positive ε_Hf(t) values (+7.11 to +13.87). Moreover, they show high La/Nb (1.79–2.87) and low La/Ba (0.02–0.08) ratios. Such features indicate that they were derived from partial melting of lithospheric mantle that had been modified by fluids. The intermediate-felsic volcanic rocks consist of trachydacite and andesite, which show medium SiO₂ concentrations (58.31–66.44 wt. %), a wide range of Mg^# values (28–53) and with A₁-type granites affinities. These features, along with slightly positive to negative ε_Hf(t) values (+0.53 to ?17.71), indicate that they originated from mixed magma of melted lower crust and mantle substances. Dacites from dikes are distinguished by high SiO₂ concentrations (65.72–67.2 wt. %), negative ε_Hf(t) values (?2.55 to ?6.72) and old zircon Hf T_DM2 ages (1453–1653 Ma), suggesting they were generated by melting of Mesoproterozoic and Palaeoproterozoic crustal material. All of the investigated volcanic and sub-volcanic rocks exhibit geochemical signatures of extension setting. In combination with previous studies, we suggest the Early Cretaceous extension in northeast China is related to the collapse of thickened lithosphere after closure of the Mongol–Okhotsk Ocean and to the slab break off of the Mudanjiang Ocean.     

Sr,Nd and Pb isotopic and geochemical constraints for the origin of magmas in Popocatépetl volcano (central Mexico) and their relationship with the adjacent volcanic fields

We present new geochemical data (major- and trace-elements, as well as Sr and Nd isotopic compositions) of volcanic rocks erupted from Popocatépetl volcano during the volcanic event from December 2000 to January 2001. These data along with an exhaustive compilation of geochemical and Sr, Nd, and Pb isotope data reported for Popocatépetl rocks and nearby volcanic areas are used to examine the origin and geochemical evolution of the magmas in the central Mexican volcanic belt (CMVB). During this period of volcanic eruptions Popocatépetl produced ash columns as high as 7 km. Pyroclastic flows and lahars were observed after the completion of the activity. Samples of banded pumice and a bomb fragment transported by the lahar were chemically analysed for this work. Rocks show an andesitic composition with 58.5–61.7 wt.% SiO₂ and 5.9–4.0 wt.% MgO. Contents of large ion lithophile elements (LILE), rare-earth elements (REE) and Zr are nearly constant through the compositional range. No significant Eu anomaly is present, but the samples show Nb-anomaly relative to LILE and high-field strength elements (HFSE). Nd- and Sr-isotopic compositions of these samples range from ¹⁴³Nd/¹⁴⁴Nd = 0.51291 to 0.51287 and ⁸⁷Sr/⁸⁶Sr = 0.70399 to 0.70422. Comparison of Popocatépetl products with volcanic rocks from the nearby areas shows that the magmas in CMVB were generated in a heterogeneously veined-mantle source enriched in LILE, HFSE, and REE. Additional crustal assimilation as well as fractional crystallization could account for the great chemical variability of rocks in the CMVB. Statistical comparison of the geochemical compositions of the volcanic products ejected from 1994 to 2000 to those ejected during the 2001 event shows that most geochemical parameters (major- and trace-elements, normative minerals, Sr and Nd isotopic composition, as well some elemental ratios) present no statistically significant differences. Statistically significant differences in the mean only were computed for the major-elements SiO₂, FeO, MgO, CaO, and K₂O, as well as for the rare-earth elements Nd, Sm, Eu, Gd, Dy, Ho, Tm, and Yb.     

Petrogenesis and tectonic implications of the middle Silurian volcanic rocks in northern West Junggar,NW China

Zircon U–Pb geochronological and geochemical analyses are reported for a suite of the middle Silurian volcanic rocks from northern West Junggar (NW China), southern Central Asian Orogenic Belt (CAOB), with the aim to investigate the sources, petrogenesis, and tectonic implications. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U–Pb analysis from an andesite yielded a concordant weighted mean ²⁰⁶Pb/²³⁸U age of 429 ± 3 Ma, indicating the presence of middle Silurian volcanic rocks in northern West Junggar. The andesite is tholeiite series and characterized by minor variations in compositions (SiO₂ = 55.68–59.17 wt.%, Al₂O₃ = 14.56–17.7 wt.%, TiO₂ = 0.55–1.23 wt.%, Na₂O + K₂O = 3.46–7.16 wt.%, and P₂O₅ = 0.15–0.37 wt.%), with wider MgO content (2.18–6.48 wt.%) and Mg# (57.4–77.9). All andesitic rocks are enriched in large-ion lithophile elements (LILEs; e.g. Rb, Ba, K, and Th) and light rare earth elements (LREEs), but strongly depleted in some high field strength elements (HFSEs; e.g. Nb, Ta and Ti), with slight negative Eu anomalies (Eu/Eu* = 0.8–1). These features suggest that the andesitic magmas were derived from 2–8% partial melting of a garnet lherzolite depleted mantle source with subducted sediments metasomatized by slab-derived fluids. Combining the current study with those data in existing literature, we conclude that the middle Silurian volcanic rocks formed in an intra-oceanic subduction setting during consumption of the Irtysh–Zaysan Ocean, and further confirm the eastern extension of the early Palaeozoic Boshchekul–Chingiz volcanic arc of East Kazakhstan in China.     

Petrogenesis and tectonic implications of early Carboniferous alkaline volcanic rocks in Karamay region of West Junggar,Northwest China

ABSTRACT

Zircon U–Pb geochronological and geochemical analyses are reported for a suite of the early Carboniferous volcanic rocks from West Junggar (Northwest China), southern Central Asian Orogenic Belt (CAOB), with the aim to investigate the sources, petrogenesis, and tectonic implications. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U–Pb analysis from an andesite yielded concordant weighted mean ²⁰⁶Pb/²³⁸U age of 345 ± 3 Ma, indicating the presence of early Carboniferous volcanic rocks in West Junggar. The early Carboniferous volcanic rocks consist of basalt, basaltic andesite, and andesite. Geochemically, all the samples bear the signature of ocean island basalt (OIB), and are characterized by alkaline affinity with minor variations in SiO₂ compositions (45.13–53.05 wt.%), high concentrations of Na₂O + K₂O (5.08–8.89 wt.%) and TiO₂ (1.71–3.35 wt.%), and LREE enrichment and HREE depletion ((La/Yb)_N = 7.1–12.4), with weak Eu anomalies (Eu/Eu* = 0.9–1.1) and no obvious Nb, Ta, and Ti negative anomalies. These features suggest that the early Carboniferous volcanic rocks were derived from an OIB-related source that consists of oceanic lithosphere with ~1–3% degree partial melting of garnet lherzolite. From these observations, in combination with previous work, we conclude that the early Carboniferous alkaline volcanic rocks in Karamay region formed by upwelling of asthenospheric mantle through a slab window in a forearc setting during consumption of the West Junggar Ocean. Meanwhile, seamounts, which formed in the Late Devonian and were accreted and subducted in Karamay arc, also brought geological effects in the subduction zone.     

Chemical composition,volatile components,and trace elements in melts of the Karymskii volcanic center,Kamchatka, and Golovnina volcano,Kunashir Island: Evidence from inclusions in minerals

Melt inclusions were examined in phenocrysts in basalt, andesite, dacite, and rhyodacite from the Karymskii volcanic center in Kamchatka and dacite form Golovnina volcano in Kunashir Island, Kuriles. The inclusions were examined by homogenization and by analyzing glasses in more than 80 inclusions on an electron microscope and ion microprobe. The SiO₂ concentrations in the melt inclusions in plagioclase phenocrysts from basalts from the Karymskii volcanic center vary from 47.4 to 57.1 wt %, these values for inclusions in plagioclase phenocrysts from andesites are 55.7–67.1 wt %, in plagioclase phenocrysts from the dacites and rhyodacites are 65.9–73.1 wt %, and those in quartz in the rhyodacites are 72.2–75.7 wt %. The SiO₂ concentrations in melt inclusions in quartz from dacites from Golovnina volcano range from 70.2 to 77.0 wt %. The basaltic melts are characterized by usual concentrations of major components (wt %): TiO₂ = 0.7–1.3, FeO = 6.8–11.4, MgO = 2.3–6.1, CaO = 6.7–10.8, and K₂O = 0.4–1.7; but these rocks are notably enriched in Na₂O (2.9–7.4 wt % at an average of 5.1 wt %, with the highest Na₂O concentration detected in the most basic melts: SiO₂ = 47.4–52.0 wt %. The concentrations of volatiles in the basic melts are 1.6 wt % for H₂O, 0.14 wt % for S, 0.09 wt % for Cl, and 50 ppm for F. The andesite melts are characterized by high concentrations (wt %) of FeO (6.5 on average), CaO (5.2), and Cl (0.26) at usual concentrations of Na₂O (4.5), K₂O (2.1), and S (0.07). High water concentrations were determined in the dacite and rhyodacite melts: from 0.9 to 7.3 wt % (average of 15 analyses equals 4.5 wt %). The Cl concentration in these melts is 0.15 wt %, and those of F and S are 0.06 and 0.01 wt %, respectively. Melt inclusions in quartz from the dacites of Golovnina volcano are also rich in water: they contain from 5.0 to 6.7 wt % (average 5.6 wt %). The comparison of melt compositions from the Karymskii volcanic center and previously studied melts from Bezymyannyi and Shiveluch volcanoes revealed their significant differences. The former are more basic, are enriched in Ti, Fe, Mg, Ca, Na, and P but significantly depleted in K. The melts of the Karymskii volcanic center are most probably less differentiated than the melts of Bezymyannyi and Shiveluch volcanoes. The concentrations of water and 20 trace elements were measured in the glasses of 22 melt inclusions in plagioclase and quartz from our samples. Unusually high values were obtained for Li concentrations (along with high Na concentrations) in the basaltic melts from the Karymskii volcanic center: from 118 to 1750 ppm, whereas the dacite and rhyolite melts contain 25 ppm Li on average. The rhyolite melts of Golovnina volcano are much poorer in Li: 1.4 ppm on average. The melts of the Karymskii volcanic center are characterized by relative minima at Nb and Ti and maxima at B and K, as is typical of arc magmas.     

Melt inclusion constraints on volatile systematics and degassing history of the 2014–2015 Holuhraun eruption,Iceland

The mass of volatiles emitted during volcanic eruptions is often estimated by comparing the volatile contents of undegassed melt inclusions, trapped in crystals at an early stage of magmatic evolution, with that of the degassed matrix glass. Here we present detailed characterisation of magmatic volatiles (H₂O, CO₂, S, Fl and Cl) of crystal-hosted melt and fluid inclusions from the 2014–2015 Holuhraun eruption of the Bárðarbunga volcanic system, Iceland. Based on the ratios of magmatic volatiles to similarly incompatible trace elements, the undegassed primary volatile contents of the Holuhraun parental melt are estimated at 1500–1700 ppm CO₂, 0.13–0.16 wt% H₂O, 60–80 ppm Cl, 130–240 ppm F and 500–800 ppm S. High-density fluid inclusions indicate onset of crystallisation at pressures?≥?0.4 GPa (~?12 km depth) promoting deep degassing of CO₂. Prior to the onset of degassing, the melt CO₂ content may have reached 3000–4000 ppm, with the total magmatic CO₂ budget estimated at  23–55 Mt. SO₂ release commenced at 0.12 GPa (~?3.6 km depth), eventually leading to entrapment of SO₂ vapour in low-density fluid inclusions. We calculate the syn-eruptive volatile release as 22.2 Mt of magmatic H₂O, 5.9–7.7 Mt CO₂, and 11.3 Mt of SO₂ over the course of the eruption; F and Cl release were insignificant. Melt inclusion constraints on syn-eruptive volatile release are similar to estimates made during in situ field monitoring, with the exception of H₂O, where field measurements may be heavily biased by the incorporation of meteoric water.     

Silicate and salt melts in the genesis of the industrial’noe tin deposit: Evidence from inclusions in minerals

The data obtained on melt and fluid inclusions in minerals of granites, metasomatic rocks, and veins with tin ore mineralization at the Industrial’noe deposit in the southern part of the Omsukchan trough, northeastern Russia, indicate that the melt from which the quartz of the granites crystallized contained globules of salt melts. Silicate melt inclusions were used to determine the principal parameters of the magmatic melts that formed the granites, which had temperatures at 760–1020°C, were under pressures of 0.3–3.6 kbar, and had densities of 2.11–2.60 g/cm³ and water concentrations of 1.7–7.0 wt %. The results obtained on the fluid inclusions testify that the parameters of the mineral-forming fluids broadly varied and corresponded to temperatures at 920–275°C, pressures 0.1–3.1 kbar, densities of 0.70–1.90 g/cm³, and salinities of 4.0–75.0 wt % equiv. NaCl. Electron microprobe analyses of the glasses of twelve homogenized inclusions show concentrations of major components typical of an acid magmatic melt (wt %, average): 73.2% SiO₂, 15.3% Al₂O₃, 1.3% FeO, 0.6% CaO, 3.1% Na₂O, and 4.5% K₂O at elevated concentrations of Cl (up to 0.51 wt %, average 0.31 wt %). The concentrations and distribution of some elements (Cl, K, Ca, Mn, Fe, Cu, Zn, Pb, As, Br, Rb, Sr, and Sn) in polyphase salt globules in quartz from both the granites and a mineralized miarolitic cavity in granite were assayed by micro-PIXE (proton-induced X-ray emission). Analyses of eight salt globules in quartz from the granites point to high concentrations (average, wt %) of Cl (27.5), Fe (9.7), Cu (7.2), Mn (1.1), Zn (0.66), Pb (0.37) and (average, ppm) As (2020), Rb (1850), Sr (1090), and Br (990). The salt globules in the miarolitic quartz are rich in (average of 29 globules, wt %) Cl (25.0), Fe (5.4), Mn (1.0), Zn (0.50), Pb (0.24) and (ppm) Rb (810), Sn (540), and Br (470). The synthesis of all data obtained on melt and fluid inclusions in minerals from the Industrial’noe deposit suggest that the genesis of the tin ore mineralization was related to the crystallization of acid magmatic melts. Original Russian Text@ V.B. Naumov, V.S. Kamenetsky, 2006, published in Geokhimiya, 2006, No. 12, pp. 1279–1289.     

Origin of high-An plagioclase in the early Permian (~280 Ma) Xiaohaizi wehrlite,Northwest China: insights from melt inclusions in clinopyroxene macrocrysts and zircon oxygen isotopes

ABSTRACT

The Xiaohaizi wehrlite intrusion in the early Permian Tarim Large Igneous Province, Northwest China, is characterized by unusual high-An (up to 86) plagioclases. It has been suggested that H₂O may have exerted a major control on their formation, but this interpretation requires further direct evidence. Moreover, it remains unclear where the water came from. In order to unravel these questions, we present electron microprobe analyses of minerals and melt inclusions in clinopyroxene macrocrysts in the dikes crosscutting the Xiaohaizi wehrlite intrusion and in situ oxygen isotope data of zircons from the Xiaohaizi wehrlite. The homogenized melt inclusions have restricted SiO₂ (45.5–48.7 wt.%) and Na₂O + K₂O (2.4–3.8 wt.%) contents, displaying sub-alkaline affinity. This is inconsistent with the alkaline characteristic of the parental magma of the clinopyroxenes, suggesting significant modification of melt inclusions by contamination of the host clinopyroxene due to overheating. Nevertheless, the Ca/Na ratios (2.9–4.7) of melt inclusions are the upper limit of the parental magma of the clinopyroxenes due to high CaO (21.5–23.0 wt.%) and very low Na₂O (0.22–0.34 wt.%) contents in the host clinopyroxenes. Thermodynamic calculation suggests that under fixed P (2.7 kbar) and T (1000°C), and assumed H₂O (~1.5 wt.%) conditions, the Ca/Na ratio of the parental magma cannot generate high-An plagioclase in the wehrlite. The results confirm that H₂O exerts a major control. Zircon δ¹⁸O (VSMOW) values (2.99–3.71‰) are significantly lower than that of mantle-derived zircon (5.3 ± 0.6‰). Such low zircon δ¹⁸O values may be due to incorporation of large amounts of low-δ¹⁸O, hydrothermally altered oceanic crust. However, geochemical and Sr-Nd-Pb isotopic data do not support recycled oceanic crust in the mantle source of the Xiaohaizi intrusion. Alternatively this can be explained by incorporation of meteoritic water in the magma chamber. This will increase the H₂O content of the liquid that finally crystallize high-An plagioclases.     

Investigation on mantle peridotites from Neyriz ophiolite, south of Iran: geodynamic signals

Neyriz ophiolite in Abadeh Tashk area appears as four major separated massifs in an area with 125 km², south of Iran. Peridotites including harzburgite, dunite, and lesser low-Cpx lherzolite are the major constituents of the ophiolite with very minor mafic rocks. Usual gabbros of ophiolite complexes are virtually absent from the study area. Mineral modality associated with bulk rock and mineral chemistry of the peridotites show a progression from fertile to ultra-refractory character, reflected by a progressive decrease in modal pyroxenes and in Al₂O₃, CaO, SiO₂, Sc, Ta, V, and Ga values of the studied rocks by approaching chromite deposits. The Neyriz peridotites vary from low-Cpx lherzolite (MgO, 41.97–43.1 wt.%; Al₂O₃, 0.8–1.3 wt.%) with low content of Cr# spinel (36.7–37.6) and Fo olivine (90.79–91.5) to harzburgite (MgO, 44.31–45.25 wt.%;Al₂O₃, 0.29–0.45 wt.%; Cr# spinel, 58.2–73.45; Fo olivine, 91.23–91.56), and then to dunite (MgO, 45.9–49.2 wt.%; Al₂O₃, 0.18–0.48 wt.%) with higher content of Cr# spinel (74.34–79.36) and Fo olivine (91.75–94.68). Compared to modern oceanic settings, mineral and rock composition of low-Cpx lherzolite plot within the field of mid-ocean-ridge environment, whereas those of harzburgite and dunite fall in the field of fore-arc peridotites. As a result of the studies on minerals and whole rock chemistry along with rock interrelationships, we contend that the peridotites were subsequently affected by percolating hydrous boninitic melt from which the high-Cr–Mg, low-Ti chromitites were formed within mantle wedge above the supra-subduction zone in a fore-arc setting.     

Post-caldera dacites from the Santorini volcanic complex,Aegean Sea,Greece: an example of the eruption of lavas of near-constant composition over a 2,200 year period

The post-caldera Kameni islands of the Santorini volcanic complex, Aegean Sea, Greece are entirely volcanic and were formed by eleven eruptions between 197 B.C. and 1950. Petrographic, mineral chemical and whole-rock major and trace element data are presented for samples of lava collected from the products of seven eruptive cycles which span the entire period of activity. The main phenocryst phases are plagioclase, clinopyroxene, orthopyroxene and titaniferous magnetite, which are weakly zoned (e.g. plagioclase — An₅₅ to An₄₂). The lavas are typical calc-alkaline dacites and show a restricted range of composition (from 64.1 to 68.4 wt. % SiO₂). The phenocrysts were in equilibrium with the melts at temperatures of 960–1012 °C, pressures of 800–1500 bars and oxygen fugacities of 10^–9.6-10^–9.9 bars. The pre-eruptive water content of the magmas was 3–4 wt. % but since the lavas contain only 0.1–0.4 wt. % H₂O, a considerable amount (about 0.01–0.015 km³) of water was lost prior to or during eruption. This indicates that the magmas rose to the surface gradually allowing the (largely) non-explosive loss of volatiles. The lavas were probably extruded initially from more or less cylindrical conduits which developed into fissures as the eruptions proceeded. The post-caldera lavas evolved from more mafic parental magmas (basalt-andesite) via fractional crystallization. The small range of compositional variation shown by these lavas can be explained in terms of near-equilibrium crystallization. Analyses of samples of lavas belonging to single eruption cycles and to individual flows indicate that the underlying magma chamber is compositionally zoned. The average composition of erupted magma has remained approximately constant since 1570 A.D. but that fact that the 197 B.C. magma was sligthly richer in SiO₂ provides additional evidence that the magma chamber is compositionally zoned. Crystal settling has not affected the composition of the magma over a 2,200 year period of time which indicates that the melts do not behave as Newtonian fluids. Zonation was thus probably established prior to the 197 B.C. eruption though it is possible that it is developed and maintained by crystal-liquid differentiation processes other than crystal settling (e.g. boundary layer crystallization). The data indicate that there has been no significant cooling during 2,200 years; the maximum amount of cooling is <50 °C and is probably less than 30 °C. Two hypotheses are considered to explain the thermal and chemical buffering of the post-caldera magma chamber: (i) The magma chamber is large and heat losses due to conduction are largely compensated by latent heat supplied by thick, partially crystalline cumulate sequences. (ii) Periodic influx of hot mafic magma, which does not mix with the dacitic magma, inhibits cooling. The second alternative is favored because the post-caldera lavas differ geochemically from the pre-caldera lavas which signifies that a new batch of magma was formed and/or emplaced after the catastrophic eruption of 1390 B.C., and hence that mafic magmas may still be reaching upper crustal levels.     

Geochemical and geochronological constraints on Late Jurassic volcanic rocks at Tuen Mun,Hong Kong,with implications for the Palaeo-Pacific subduction

Widespread Mesozoic igneous rocks in Hong Kong form part of the giant Mesozoic igneous province in Southeastern China. The Tuen Mun Formation in the Northwestern New Territories is the oldest volcanic unit known in Hong Kong. This formation contains a lower unit composed of dominantly volcanic breccia, minor dacite, rhyolite, and tuff, and an upper unit of basaltic andesitic to andesitic lava. The volcanic rocks from the lower unit contain zircon grains with a mean U–Pb age of 163.4 ± 0.9 Ma, synchronous with the adjacent Tsuen Wan Volcanic Group in the region. Good inter-correlations between different elements in the Harker diagrams indicate that the volcanic rocks with high SiO₂ (e.g. >65 wt.%) are essentially physical mixtures of intermediate magmas and various xenoliths of country rocks, characterizing the palaeo-volcanic plug facies. Preservation of large amounts of xenoliths of sandstone and marble in the volcanic rocks, which is revealed both in field and under microscopic observation, further supports this hypothesis. The original andesitic magma, represented by the intermediate volcanic rocks with SiO₂ <65 wt.%, exhibit enrichments of LILEs and LREEs compared with N-MORB, but have negative Nb–Ta–Ti anomalies in the primitive-mantle normalized diagram, similar to those derived from metasomatized mantle wedge in an arc environment. Large ranges of SiO₂, MgO, and CaO contents, and negative Eu and Ce anomalies are consistent with significant fractional crystallization of likely olivine/pyroxene and plagioclase. We propose that during the Late Jurassic subduction of the Palaeo-Pacific Plate underneath the coastal continental arc in Southeast China generated prolonged and cyclic volcanism in the northern part of Hong Kong.     

Silicate globules in kyanite from grospydites of the Zagadochnaya kimberlite pipe,Yakutia: The problem of the origin

The results of complex study of silicate globules and α-quartz paramorphs after coesite in kyanite from grospydites from the Zagadochnaya kimberlite pipe, Yakutia, using optical and scanning electron spectroscopy, electron and ion microprobes, LA ICP MS and Raman spectroscopy, are presented. The existence of radial fractures diverging from silicate globules into the matrix (kyanite) attests to the fact that the content of the globules is extremely condensed. A zonal structure is usually typical for globules: a coat and a core, which can be explicitly distinguished under the electron microscope, can be differentiated in them. Compositionally, the coat of the globule corresponds to potassium feldspar (wt %: 66.4 SiO₂; 16.9 Al₂O₃; 0.4 FeO; 0.1 CaO; 0.2 Na₂O; 14.7 K₂O). The globules were also detected in which along with K, a high content of Na and Ca was also ascertained in the silicate coat. The globule coat is considerably enriched with Ba, La, Ce, Nb, and a number of other noncompatible elements as compared with xenolith minerals. The water content in globules is ∼0.6 wt %. As compared with the host mineral (kyanite), the core part of the globules is also enriched with Co, Ni, Zn, and Cu; their content in kyanite is negligibly low. The entire data collection attests to the fact that the formation of silicate globules could have been caused by interaction of the conservated fluid and/or water-silicate melt with the host mineral and crystalline inclusions of clinopyroxene and garnet with decreasing pressure during the transportation of grospydite xenoliths by the kimberlite melt to the Earth’s surface.     

Geochronology,geochemistry, and petrogenesis of the Maçka subvolcanic intrusions: implications for the Late Cretaceous magmatic and geodynamic evolution of the eastern part of the Sakarya Zone,northeastern Turkey

The Maçka subvolcanic intrusions (MSIs) in the eastern part of the Sakarya zone, northeastern Turkey, play a critical role in understanding the petrogenetic and geodynamic processes that took place during the growth of Late Cretaceous arc crust of this region. U–Pb zircon (79.97 ± 0.97 Ma) and two ⁴⁰Ar–³⁹Ar amphibole ages (average 81.37 ± 0.5 Ma) indicate that the MSIs were emplaced in Late Cretaceous (Campanian) time into the coeval volcanic rocks. A slightly younger zircon fission track (FT) age (73 ± 9 Ma) points to a rapid exhumation and cooling after crystallization. The intrusions are observed in areas less than 1 km² in the field and contain abundant mafic microgranular enclaves (MMEs). The host rocks (HRs) are entirely composed of tonalite (SiO₂ = 63–65 wt.%, Mg# = 43–52), and the MMEs are gabbro-diorite in composition (SiO₂ = 53–57 wt.%, Mg# = 45–48). Both the HRs and the MMEs are I-type, high-K calc-alkaline in composition and display a metaluminous character. They are characterized by geochemical features typical for magmas of subduction-related environments. Chondrite-normalized REE patterns are moderately fractionated [(La/Yb)_N = 6–11] and display slightly negative Eu anomalies (Eu/Eu* = 0.7–0.9), with weak concave-upward REE patterns, suggesting that amphibole fractionation played a role during their evolution. The MMEs have slightly different I_Sr (0.7081–0.7085) and ε_Nd (?5.0 to ?5.4) values compared with those of their HRs (I_Sr = 0.7084–0.7087 and ε_Nd = ?5.7 to ?6.9), indicating that variable amounts of crustal and mantle components were involved in the generation of parental magma to these rocks. All of these data, combined with those of previous regional studies, suggest that the MSIs are hybrid in origin, produced by the mixing of enriched lithospheric mantle- and lower crust-derived melts in an extensional arc setting that was caused by slab rollback.     

Abundances of F,Cl S and P in Volcanic Magmas and Their Evolution,Wudalianchi

F, Cl, S and P were determined, using electron microprobe, in magmatic inclusions trapped within minerals and glass mesostasis from Wudalianchi volcanic rocks. The initial volcanic magma from Wudalianchi corresponds to the basanitic magma crystallized near the surface ( pressure < 91 Mpa ). The potential H₂O content of this magma is in the range 2 — 4 wt. %. The initial composition of volcanic magmas varies regularly from early to late volcanic events. From the Middle Pleistocene to the recent eruptions (1719 – 1721 yr.), the basicity of volcanic magma tends to increase, as reflected by an increase in MgO and CaO contents and by a progressive decrease in SiO₂ and K₂O contents. Meanwhile. from early (Q₂ ) to late (Q₃) episodic eruptions of the Middle Pleistocene, the initial concentrations of chlorine in volcanic magmas range from 1430 – 1930 ppm to 1700 ppm and decrease to 700 — 970 ppm for the first episodic eruption during the Holocene (Q ₄ ¹ ). The chlorine concentrations of volcanic magmas of recent eruption (Q ₄ ² ) are increased again to 2600 – 2870 ppm. A parallel evolution trend for phosphorus and chlorine concentrations in magmas has been certified: 1500 – 5970 ppm (Q₂)→ 3500 – 4210 ppm (Q₃)→ 1100– 3500 ppm (Q ₄ ¹ )→ 6800– 7900 ppm (Q ₄ ² ). The fluorine contents of volcanic magmas, from early to late volcanic events, show the same trend: 770 – 2470 ppm → 200–700 ppm → 700 – 800 ppm. During the crystallization-evolution of volcanic magmas, fluorine and phosphorus tend to be enriched in residual magmas as a result of crystal-melt differentiation. for example. the fluorine contents reach 5000– 6800 ppm and the phosphorus contents, 2.93wt.% in residual magmas. An appreciable amount of chlorine may be lost from water rich volcanic magmas prior to eruption as a result of degassing. Apparently, water serves as a gas carrier for the chlorine. The chlorine contents of residual magmas may decrease to 100 – 300 ppm. The volcanic magmas from Wudalianchi are poor in sulfur, normally ranging from 200 to 400ppm. On account of the behavior of sulfur in magmas and the strontium and oxygen isotopic analyses ((⁸⁷Sr /⁸⁶Sr)_i=0.70503– 0.70589; δ¹⁸O = + 5.50 – + 6.89 ‰ ), it can be considered that the basanitic magmas in the Wudalianchi volcanic area came from the upper mantle and have not yet been contaminated probably by continental crust materials.     

Chemical composition and crystallization conditions of trachybasalts from the Dzhida field, Southern Baikal volcanic area: Evidence from melt and fluid inclusions

Melt and fluid inclusions have been studied in olivine phenocrysts (Fo 81–79) from trachybasalts of the Southern Baikal volcanic area, Dzhida field. The melt inclusions were homogenized, quenched, and analyzed on an electron and ion microprobe. The study of homogenized glasses of nine inclusions showed that basaltic melts (SiO₂ = 47.1–50.3 wt %, MgO = 5.0–7.7 wt %, CaO = 7.1–11.1 wt %) have high contents of Al₂O₃ (17.1–19.6 wt %), Na₂O (4.1–6.2 wt %), K₂O (2.2–3.3 wt %), and P₂O₅ (0.6–1.1 wt %). The volatile contents are low (in wt %): 0.24–0.31 H₂O, 0.08 F, 0.03 Cl, and 0.02 S. Primary fluid inclusions in olivines from four trachybasalt samples contain high-density CO₂ (0.73–0.87 g/cm³), indicating a CO₂ fluid pressure of 4.3–6.6 kbar at 1200–1300°C and olivine crystallization depths of 16–24 km. Ion microprobe analyses of 20 glasses from melt inclusions for trace elements showed that the magmas of the Baikal rift were enriched in incompatible elements, thus differing from oceanic rift basalts and resembling oceanic island basalts. A comparison of our data on melt and fluid inclusions in olivine from trachybasalts of the Dzhida field with preexisting data on the Eastern Tuva volcanic highland in the Southern Baikal volcanic area showed that they had similar contents of volatiles, major, and trace elements.     

Mineralogy, conditions of crystallization and melt generation of epidote-bearing porphyries from the Middle Urals, Russian federation

Epidote-bearing porphyritic dikes (whole rock analysis: SiO₂?=?55–65 wt. %, MgO <2.1 wt. %, K₂O <2.5 wt. %, Al₂O₃ >17 wt. %, Na₂O + K₂O?=?5.7–9.4 wt. %) situated in the continental margin zone, the Middle Urals, Russian Federation have been dated using SHRIMP U-Pb zircon techniques and give a Middle Devonian age of 388?±?2 Ma and 389?±?6 Ma. The porphyries contain phenocrysts of magmatic epidote (Ps?=?17–25 %), Ca- and Mn-rich (CaO >9 wt. %; MnO >6 wt. %) almandine garnet, Al-rich (Al₂O₃?=?12–16 wt. %) amphibole, titanite, plagioclase, biotite, muscovite, apatite, and quartz. 60 to 70 % groundmass of the porphyritic dikes consists of fine-grained albite, quartz, and K-feldspar. A variety of thermobarometric estimations, plus comparison with published experimental data indicate that the phenocryst assemblage was stable between 5 and 11 kbar and 690 to 800 °C. Oxygen fugacity was close to or greater than logfo₂ = Ni-NiO + 1. Later stage formation of the quartz-feldspar groundmass took place at hypabyssal conditions, corresponding to 1 to 2 kbar and 660 to 690 °C. The porphyritic dikes are metaluminous to slightly peraluminous (ACNK?=?0.7–1.17). They are enriched in REE and depleted Nb and Ti. They show features typical of subduction-related magmas. Chemical composition and isotopic ratios of ⁸⁶Sr/⁸⁷Sr_i?=?0.709–0.720 suggest that both mantle- and deep crustal-derived materials were involved in their petrogenesis.     

Phase relations in fluorine-bearing granite and nepheline syenite systems at 800°C and 1 kbar

The data obtained on the sodic part of the SiO₂-Al₂O₃-Na₂O-K₂O system with F at 800°C and 1 kbar provide the basis for constructing a phase diagram showing the region of an aluminosilicate melt. In this system, oxide and fluoride phases are identified that control the stability field of the melt and the solubility of F. Liquid immiscibility was detected in aluminous nepheline-and quartz-normative Li-bearing compositions (the latter compositions are characterized by a wider immiscibility field). Solubility of F was determined in an aluminosilicate melt saturated with respect to F, i.e., coexisting with phases rich in this element. The F concentrations in the glasses range from 2 to 20 wt %. The quartz-normative glasses are poorer in F (no more than 5 wt % F) than the nepheline-normative glasses (which contain mostly 5–10 wt % F). The maximum F concentrations (> 10 wt %) in the phase diagram lie on both sides of the albite composition point in the region of ultragpaitic nepheline-normative melts and in the region of normal syenite melts. Changes in the phase relations when Na is substituted for K were determined in the quartz-normative silicate melt.     

Volatiles H2O,CO2, and Cl in a subduction related basalt

The products of the 1974 eruption of Fuego, a subduction zone volcano in Guatemala, have been investigated through study of silicate melt inclusions in olivine. The melt inclusions sampled liquids in regions where olivine, plagioclase, magnetite, and augite were precipitating. Comparisons of the erupted ash, groundmass, and melt inclusion compositions suggest that the inclusions represent samples of liquids present in a thermal boundary layer of the magma body. The concentrations of H₂O and CO₂ in glass inclusions were determined by a vacuum fusion manometric technique using individual olivine crystals (Fo77 to Fo71) with glass inclusion compositions that ranged from high-alumina basalt to basaltic andesite. Water, Cl, and K₂O concentrations increased by a factor of two as the olivine crystals became more iron-rich (Fo77 to Fo71) and as the glass inclusions increased in SiO₂ from 51 to 54 wt.% SiO₂. The concentration of H₂O in the melt increased from 1.6 wt.% in the least differentiated liquid to about 3.5% in a more differentiated liquid. Carbon dioxide is about an order of magnitude less abundant than H₂O in these inclusions. The gas saturation pressures for pure H₂O in equilibrium with the melt inclusions, which were calculated from the glass inclusion compositions using the solubility model of Burnham (1979), are given approximately by P(H₂O)(Pa)=(SiO₂−48.5 wt.%) × 1.45 × 10⁷. The concentrations of water in the melt and the gas saturation pressures increased from about 1.5% to 3.5% and from 300 to 850 bars, respectively, during pre-eruption crystallization.     

Geochemistry and zircon U–Pb chronology of charnockites in the Yinshan Block,North China Craton: tectonic evolution involving Neoarchaean ridge subduction

The Yinshan Block, part of the Neoarchaean basement of the Western Block of the North China Craton, is composed of granite–greenstone and granulite–charnockite complexes. We report research on a suite of charnockites from the granulite–charnockite complex and characterize their geochemistry, zircon U–Pb geochronology, and Hf isotopic composition. The charnockites can be divided into intermediate (SiO₂ = 59–63 wt.%) and silicic (SiO₂ = 69–71 wt.%) groups. U–Pb zircon data yield protolith formation ages of 2524 ± 4 Ma, 2533 ± 15 Ma, followed by metamorphism at 2498 ± 3 Ma, 2490 ± 11 Ma, respectively, for these groups. Although the intermediate charnockites are characterized by higher Al₂O₃, TiO₂, Fe₂O₃^T, MnO, MgO, CaO, P₂O₅, K₂O, Sr, and ΣREE content than the silicic charnockites, the ages and Hf isotopic composition of zircons and REE patterns of both intermediate and silicic charnockites are remarkably consistent, which indicates that they are genetically related. These charnockites are predominantly metaluminous to slightly peraluminous, calc-alkalic to calcic, and magnesian – characteristics generally related to a subduction setting. High-Sr + Ba granites with low K₂O/Na₂O characteristics, shown by these charnockites, imply a mixture of mafic and felsic magmas generated from an enriched mantle + lower crust. High MgO, Ni, Cr and Mg#, low K₂O/Na₂O, and metaluminous to slightly peraluminous natures imply that the source rocks most likely were amphibolites. Coeval calc-alkaline magmatism and high-T granulite-facies metamorphism under low-H₂O activity in the area lead us to propose a model involving mid-ocean ridge subduction within a Neoarchaean convergent margin. The arc-related rocks accreted along the continent margin, and became a barrier when the lithospheric mantle ascended through the slab window. Melt derived from the decompressing mantle mixed with melt derived from the overlying, juvenile lower crust melt, which was warmed and metamorphosed by the ascending lithospheric mantle.