Water contents of the Cenozoic lithospheric mantle beneath the western part of the North China Craton: Peridotite xenolith constraints

Nominally anhydrous phases (clinopyroxene (cpx), orthopyroxene (opx), and olivine (ol)) of peridotite xenoliths hosted by the Cenozoic basalts from Beishan (Hebei province), and Fansi (Shanxi province), Western part of the North China Craton (WNCC) have been investigated by Fourier transform infrared spectrometry (FTIR). The H₂O contents (wt.) of cpx, opx and ol are 30–255 ppm, 14–95 ppm and ~ 0 ppm, respectively. Although potential H-loss during xenolith ascent cannot be excluded for olivine, pyroxenes (cpx and opx) largely preserve the H₂O content of their mantle source inferred from (1) the homogenous H₂O content within single pyroxene grains, and (2) equilibrium H₂O partitioning between cpx and opx. Based on mineral modes and assuming a partition coefficient of 10 for H₂O between cpx and ol, the recalculated whole-rock H₂O contents range from 6 to 42 ppm. In combination with previously reported data for other two localities (Hannuoba and Yangyuan from Hebei province), the H₂O contents of cpx, opx and whole-rock of peridotite xenoliths (43 samples) hosted by the WNCC Cenozoic basalts range from 30 to 654 ppm, 14 to 225 ppm, and 6 to 262 ppm respectively. The H₂O contents of the Cenozoic lithospheric mantle represented by peridotite xenoliths fall in a similar range for both WNCC and the eastern part of the NCC (Xia et al., 2010, Journal of Geophysical Research). Clearly, the Cenozoic lithospheric mantle of the NCC is dominated by much lower water content compared to the MORB source (50–250 ppm). The low H₂O content is not caused by oxidation of the mantle domain, and likely results from mantle reheating, possibly due to an upwelling asthenospheric flow during the late Mesozoic–early Cenozoic lithospheric thinning of the NCC. If so, the present NCC lithospheric mantle mostly represents relict ancient lithospheric mantle. Some newly accreted and cooled asthenospheric mantle may exist in localities close to deep fault.     

Heterogeneous distribution of water in the mantle beneath the central Siberian Craton: Implications from the Udachnaya Kimberlite Pipe

The paper presents new petrographic, major element and Fourier transform infrared (FTIR) spectroscopy data and PT-estimates of whole-rock samples and minerals of a collection of 19 relatively fresh peridotite xenoliths from the Udachnaya kimberlite pipe, which were recovered from its deeper levels. The xenoliths are non-deformed (granular), medium-deformed and highly deformed (porphyroclastic, mosaic-porphyroclastic, mylonitic) lherzolites, harzburgite and dunite. The lherzolites yielded equilibration temperatures (T) and pressures (P) ranging from 913 to 1324 °C and from 4.6 to 6.3 GPa, respectively. The non-deformed and medium-deformed peridotites match the 35 mW/m² conductive continental geotherm, whereas the highly deformed varieties match the 45 mW/m² geotherm. The content of water spans 2 ± 1–95 ± 52 ppm in olivine, 1 ± 0.5–61 ± 9 ppm in orthopyroxene, and 7 ± 2–71 ± 30 ppm in clinopyroxene. The amount of water in garnets is negligible. Based on the modal proportions of mineral phases in the xenoliths, the water contents in peridotites were estimated to vary over a wide range from < 1 to 64 ppm. The amount of water in the mantle xenoliths is well correlated with the deformation degree: highly deformed peridotites show highest water contents (64 ppm) and those medium-deformed and non-deformed contain ca. 1 ppm of H₂O. The high water contents in the deformed peridotites could be linked to metasomatism of relatively dry diamondiferous cratonic roots by hydrous and carbonatitic agents (fluids/melts), which may cause hydration and carbonation of peridotite and oxidation and dissolution of diamonds. The heterogeneous distribution of water in the cratonic mantle beneath the Udachnaya pipe is consistent with the models of mantle plume or veined mantle structures proposed based on a trace element study of similar xenolithic suits. Mantle metasomatism beneath the Siberian Craton and its triggered kimberlite magmatism could be induced by mantle enrichment in volatiles (H₂O, CO₂) supplied by numerous subduction zones which surrounded the Siberian continent in Neoproterozoic-Cambrian time.     

Water content in minerals of mantle xenoliths from the Udachnaya pipe kimberlites (Yakutia)

Distribution of water among the main rock-forming nominally anhydrous minerals of mantle xenoliths of peridotitic and eclogitic parageneses from the Udachnaya kimberlite pipe, Yakutia, has been studied by IR spectroscopy. The spectra of all minerals exhibit vibrations attributed to hydroxyl structural defects. The content of H₂O (ppm) in minerals of peridotites is as follows: 23–75 in olivine, 52–317 in orthopyroxene, 29–126 in clinopyroxene, and 0–95 in garnet. In eclogites, garnet contains up to 833 ppm H₂O, and clinopyroxene, up to 1898 ppm (~ 0.19 wt.%). The obtained data and the results of previous studies of minerals of mantle xenoliths show wide variations in H₂O contents both within different kimberlite provinces and within the Udachnaya kimberlite pipe. Judging from the volume ratios of mineral phases in the studied xenoliths, the water content varies over narrow ranges of values, 38–126 ppm. At the same time, the water content in the studied eclogite xenoliths is much higher and varies widely, 391–1112 ppm.     

Stability of various hydrous phases in CMAS pyrolite-H<Subscript>2</Subscript>O system up to 25 GPa

 We carried out a series of melting experiments with hydrous primitive mantle compositions to determine the stability of dense hydrous phases under high pressures. Phase relations in the CaO–MgO–Al₂O₃–SiO₂ pyrolite with ˜2 wt% of water have been determined in the pressure range of 10–25 GPa and in the temperature range between 800 and 1400 °C. We have found that phase E coexisting with olivine is stable at 10–12 GPa and below 1050 °C. Phase E coexisting with wadsleyite is stable at 14–16 GPa and below 900 °C. A superhydrous phase B is stable in pyrolite below 1100 °C at 18.5 GPa and below 1300 °C at 25 GPa. No hydrous phases other than wadsleyite are stable in pyrolite at 14–17 GPa and 900–1100 °C, suggesting a gap in the stability of dense hydrous magnesium silicates (DHMS). We detected an expansion in the stability field of wadsleyite to lower pressures (12 GPa and 1000 °C). The H₂O content of wadsleyite was found to decrease not only with increasing temperature but also with increasing pressure. The DHMS phases could exist in a pyrolitic composition only under the conditions present in the subducting slabs descending into the lower mantle. Under the normal mantle and hot plume conditions, wadsleyite and ringwoodite are the major H₂O-bearing phases. The top of the transition zone could be enriched in H₂O in accordance with the observed increase in water solubility in wadsleyite with decreasing pressure. As a consequence of the thermal equilibration between the subducting slabs and the ambient mantle, the uppermost lower mantle could be an important zone of dehydration, providing fluid for the rising plumes. Received: 9 September 2002 / Accepted: 11 January 2003 Acknowledgements The authors are thankful to Y. Ito for the assistance with the EPMA measurement, A. Suzuki, T. Kubo and T. Kondo for technical help with the high-pressure experiments and Raman and X-ray diffraction measurements and C.R. Menako for technical support. K. Litasov thanks H. Taniguchi for his continuous encouragement and the Center for Northeast Asian Studies of Tohoku University and the Japanese Society for the Promotion of Science for the research fellowships. This work was partially supported by the Grant-in-Aid of Scientific Research of the Priority Area (B) of the Ministry of Education, Science, Sport, and Culture of the Japanese government (no. 12126201) to E. Ohtani.     

Deep carbon cycle and geodynamics: the role of the core and carbonatite melts in the lower mantle

Carbon, though being abundant in the Solar system, barely exceeds 0.01 wt.% in the silicate mantle, whereas it is ~ 3.6 wt.% in primitive chondritic meteorites that most likely formed our planet. This deficit may be due to redistribution of carbon in the liquid metal phase and then in the core at the stage of magma ocean fractionation, because carbon is much more soluble in Fe–Ni ± S melt than in silicate melts. The terrestrial heat and mass transfer are controlled mainly by layered convection and periodic peaks of plume activity as fast mantle jets that rise from the core. Plumes carry significant amounts of CO₂, H₂O, and K₂O (most probably in the form of carbonatite or hydrous carbonatite melts) released by the degassing core on its interaction with oxidized silicate material. There are two mechanisms that may maintain fast plume ascent: (1) local melting at the plume front as a result of doping with volatiles (H₂O, CO₂) as in a gas burner (rise rate 60–110 cm/yr) or (2) flow controlled by diffusion transport of silicate components in carbonatite melt (rise rate ~ 100 cm/yr).     

Ultramafic xenoliths from Lake Nyos area,Cameroon volcanic line,West-central Africa: Petrography,mineral chemistry,equilibration conditions and metasomatic features

Spinel-bearing mantle xenoliths have been recovered in the pyroclastic breccia surrounding the Lake Nyos maar. These include spinel lherzolites, spinel harzburgites and olivine websterites. They exhibit coarse granular or protogranular to weakly porphyroclastic textures, and show variations in mineral chemistry, modal compositions and equilibrium temperature. The xenoliths consist of four mineral phases typical of upper mantle origin: olivine (Fo₈₉–Fo_91.5, NiO = 0.29–0.38 wt%, CaO = 0.02–0.17 wt%), enstatite (Mg# = 90–92, Cr₂O₃ = 0.35 ± 0.04 wt%), Cr-diopside (Mg# = 92–98, Cr₂O₃ = 0.7–1.65 wt%, TiO₂ = 0.26–0.6 wt%) and spinel (high Mg# of 70–80, low TiO₂ ≤ 0.4 wt%). Spinels are aluminous (Cr# = 9.7–11) in most lherzolites, and become increasingly chromiferous from websterites (Cr#_Sp = 15.3–19.8) to harzburgites (Cr#_Sp = 19–33.6). The lherzolites are composed of olivine (48–58%), orthopyroxene (22–30%), and clinopyroxene (8–15%). The harzburgites modes are olivine (60–81%), orthopyroxene (11–29%), and clinopyroxene (<5%). The websterites are mainly composed of pyroxene (～62%) with variable amounts of olivine (23–31%). Temperatures of mineral equilibration in the xenoliths have been estimated from the two-pyroxene thermometer of Wells (1977) and range between 850 and 1050 °C, corresponding to about 10–30 kbar at a depth mantle of 30 km at least. These P–T conditions show significant variations between different petrographical types, the maximum conditions being recorded in two spinel lherzolites (NY-05 and NY-23) that have atypical chemical compositions and textures suggesting that they were initially formed in an environment close to the garnet stability field, then re-equilibrated within the spinel stability field prior to their incorporation in the host magma. With the exception of minerals from these two lherzolite nodules, all the minerals exhibit depletion of light REE, a typical feature of abyssal peridotites implying that some xenoliths from the Cameroon volcanic line were probably sampled in a part of the sub-continental mantle that is chemically similar to sub-oceanic mantle. The variations observed in the mineral chemistry and modal compositions of xenoliths suggest that the spinel harzbugite nodules which represent residues of a significant degree of partial melting of lherzolitic mantle were affected by infiltration of alkali-enriched metasomatizing melts (or fluids) within the uppermost mantle to produce pargasitic amphiboles prior to their sampling by the host lava. The features of this metasomatism event occur in the rocks of all three petrographical facies xenoliths from Lake Nyos.     

Peridotite-chromitite complexes in the Eastern Desert of Egypt: Insight into Neoproterozoic sub-arc mantle processes

The Neoproterozoic peridotite-chromitite complexes in the Central Eastern Desert of Egypt, being a part of the Arabian-Nubian Shield, are outcropped along the E–W trend from Wadi Sayfayn, Wadi Bardah, and Jabal Al-Faliq to Wadi Al-Barramiyah, from east to west. Their peridotites are completely serpentinized, and the abundance of bastite after orthopyroxene suggests harzburgite protoliths with subordinate dunites, confirmed by low contents of Al₂O₃, CaO and clinopyroxene (< 3 vol%) in bulk peridotites. The primary olivine is Fo89.3–Fo92.6, and the residual clinopyroxene (Cpx) in serpentinites contains, on average, 1.1 wt% Al₂O₃, 0.7 wt% Cr₂O₃, and 0.2 wt% Na₂O, similar in chemistry to that in Izu-Bonin-Marian forearc peridotites. The wide range of spinel Cr-number [Cr/(Cr + Al)], 0.41–0.80, with low TiO₂ (0.03 wt%), MnO (0. 3 wt%) and Y_Fe [(Fe^3 +/(Cr + Al + Fe^3 +) = 0.03 on average)] for the investigated harzburgites-dunites is similar to spinel compositions for arc-related peridotites. The partial melting degrees of Bardah and Sayfayn harzburgites range mainly from 20 to 25% and 25 to 30% melting, respectively; this is confirmed by whole-rock chemistry and Cpx HREE modelling (~ 20% melting). The Barramiyah peridotite protoliths are refractory residues after a wide range of partial melting, 25–40%, where more hydrous fluids are available from the subducting slab. The Neoproterozoic mantle heterogeneity is possibly ascribed mainly to the wide variations of partial melting degrees in small-scale areas, slab-derived inputs and primordial mantle compositions. The Sayfayn chromitites were possibly crystallized from island-arc basaltic melts, followed by crystallization of Barramiyah chromitites from boninitic melt in the late stage of subduction. The residual Cpx with a spoon-shape REE pattern is rich in both LREE and fluid-mobile elements (e.g., Pb, B, Li, Ba, Sr), but poor in HFSE (e.g., Ta, Nb, Zr, Th), similar to Cpx in supra-subduction zone (SSZ) settings, where slab-fluid metasomatism is a prevalent agent. The studied chromitites and their host peridotites represent a fragment of sub-arc mantle, and originated in an arc-related setting. The systematic increase in the volume of chromitite pods with the increasing of their host-peridotite thickness from Northern to Southern Eastern Desert suggests that the thickness of wall rocks is one factor controlling the chromitite size. The factors controlling the size of Neoproterozoic chromitite pods are the thickness, beside the composition, of the host refractory peridotites, compositions and volumes of the supplied magmas, the amount of slab-derived fluids, and possibly the partial melting degree of the host peridotites.     

Decarbonation of subducting slabs: Insight from petrological–thermomechanical modeling

Subduction of heterogeneous lithologies (sediments and altered basalts) carries a mixture of volatile components (H₂O ± CO₂) into the mantle, which are later mobilized during episodes of devolatilization and flux melting. Several petrologic and thermodynamic studies investigated CO₂ decarbonation to better understand carbon cycling at convergent margins. A paradox arose when investigations showed little to no decarbonation along present day subduction geotherms at subarc depths despite field based observations. Sediment diapirism is invoked as one of several methods for carbon transfer from the subducting slab. We employ high-resolution 2D petrological–thermomechanical modeling to elucidate the role subduction dynamics has with respect to slab decarbonation and the sediment diapirism hypothesis. Our thermodynamic database is modified to account for H₂O–CO₂ binary fluids via the following lithologies: GLOSS average sediments (H₂O: 7.29 wt.% & CO₂: 3.01 wt.%), carbonated altered basalts (H₂O: 2.63 wt.% & CO₂: 2.90 wt.%), and carbonated peridotites (H₂O: 1.98 wt.% & CO₂: 1.50 wt.%). We include a CO₂ solubility P–x[H₂O wt.%] parameterization for sediment melts. We parameterize our model by varying two components: slab age (20, 40, 60, 80 Ma) and convergence velocity (1, 2, 3, 4, 5, 6 cm year^− 1). 59 numerical models were run and show excellent agreement with the original code base. Three geodynamic regimes showed significant decarbonation. 1) Sedimentary diapirism acts as an efficient physical mechanism for CO₂ removal from the slab as it advects into the hotter mantle wedge. 2) If subduction rates are slow, frictional coupling between the subducting and overriding plate occurs. Mafic crust is mechanically incorporated into a section of the lower crust and undergoes decarbonation. 3) During extension and slab rollback, interaction between hot asthenosphere and sediments at shallow depths result in a small window (~ 12.5 Ma) of high integrated CO₂ fluxes (205 kg m^− 3 Ma^− 1).     

Stability of dense hydrous magnesium silicate phases in the systems Mg2SiO4-H2O and MgSiO3-H2O at pressures up to 27 GPa

We conducted high-pressure phase equilibrium experiments in the systems MgSiO₃ with 15 wt% H₂O and Mg₂SiO₄ with 5 wt% and 11 wt% H₂O at 20 ∼ 27 GPa. Based on the phase relations in these systems, together with the previous works on the related systems, we have clarified the stability relations of dense hydrous magnesium silicates in the system MgO-SiO₂-H₂O in the pressure range from 10 to 27 GPa. The results show that the stability field of phase G, which is identical to phase D and phase F, expands with increasing water contents. Water stored in serpentine in the descending cold slabs is transported into depths greater than 200 km, where serpentine decomposes to a mixture of phase A, enstatite, and fluid. Reaction sequences of the hydrous phases which appear at higher pressures vary with water content. In the slabs with a water content less than about 2 wt%, phase A carries water to a depth of 450 km. Hydrous wadsleyite, hydrous ringwoodite, and ilmenite are the main water reservoirs in the transition zone from 450 to 660 km. Superhydrous phase B is the water reservoir in the uppermost part of the lower mantle from 670 to 800 km, whereas phase G appears in the lower mantle only at depths greater than 800 km. In cold slabs with local water enrichment greater than 2 wt%, the following hydrous phases appear with increasing depths; phase A to 450 km, phase A and phase G from 450 km to 550 km, brucite, superhydrous phase B, and phase G from 550 km to 800 km, and phase G at depths greater than 800 km. Received: 4 August 1999 / Accepted: 1 March 2000     

Cenozoic high-K alkaline magmatism and associated Cu–Mo–Au mineralization in the Jinping–Fan Si Pan region,southeastern Ailao Shan–Red River shear zone,southwestern China–northwestern Vietnam

The Jinping–Fan Si Pan (JFP) Cenozoic magmatic and Cu–Mo–Au metallogenic belt in the southeastern part of the Ailao Shan shear zone host the Tongchang, Chang′an, Habo, and Chinh Sang Cu–Mo–Au deposits. These deposits form an integrated epithermal-porphyry regional mineralization system associated with 40–32 Ma high-K alkaline magmatism. The magmatic rocks in the belt have relatively low TiO₂ (<0.73 wt%), P₂O₅ (<0.29 wt%), and FeO^* (<4.99 wt%), and high Na₂O (2.86–4.75 wt%) and K₂O (4.01–7.98 wt%). They also have high contents of incompatible trace elements, and are enriched in LILE (Rb, Ba, K, Sr) and LREE. They have marked Nb, Ta, Ti and P depletion in primitive mantle-normalized spidergrams, and plot close to the EMII mantle field in the Sr–Nd isotopic diagram. These characteristics are similar to those of the Eocene high-K alkaline rocks along the northern Ailao Shan belt, eastern Tibet plateau. The sulfur and lead isotope analyses of sulfide minerals from both the ores and related magmatic rocks confirm the involvement of a magmatic ore fluid. The Cenozoic alkaline intrusions and Cu–Mo–Au mineralization in the JFP were formed prior to the initiation of left-lateral shearing along the Ailao Shan shear zone. The magmas appear to have been derived from enriched mantle, possibly with mixing of materials from the buried Tethyan oceanic lithosphere, and/or crust.     

Ultra-depleted peridotite xenoliths in the Northern Taihang Mountains: Implications for the nature of the lithospheric mantle beneath the North China Craton

We report the finding of peridotite xenoliths in the Early Cretaceous Longmengou olivine-bearing diabase (138 Ma) in the Northern Taihang Mountains in the central North China Craton. Based on the modal proportions of olivine, clinopyroxene, amphibole and anorthite, these peridotite xenoliths can be divided into three zones: clinopyroxene-bearing olivine zone (COZ), olivine-clinopyroxene zone (OCZ), and amphibole-bearing anorthite-clinopyroxene zone (AACZ). The core of olivine grains in clinopyroxene-bearing olivine zone have higher Mg^# (> 95), SiO₂ (41.80–42.53 wt%) and lower CaO (< 0.07 wt%), FeO (3.91–4.54 wt%) than the rim (Mg^# = 92.5–93.4, SiO₂ = 41.27–41.98 wt%, CaO = 0.20–0.34 wt%, and FeO = 7.02–8.87 wt%), suggesting that rim is reaction product. The core of olivine grains with higher Mg^# (> 95) and lower NiO content (< 0.04 wt%) in the clinopyroxene-bearing olivine zone was derived from ultra-depleted mantle subsequently altered by high Mg^# melts/magma with low Ni. Two generations of olivine grains occur in the OCZ where the first generation shows exsolution of ilmenite and magnetite rods containing up to 0.35 wt% TiO₂, and was likely derived from garnet peridotite hydrated by water. The second generation shows high Mg^# (96.2–97.1) and cataclastic texture, and was possibly formed by decomposition of the COZ. The occurrence of aluminous spinel suggests the role of melts with extremely high Al and Mg. Clinopyroxene in the AACZ shows systematic core-rim compositional variation with CaO and SiO₂ contents increasing towards the rim, and MgO and Fe₂O₃ concentrations decreasing from the core to the rim, indicating that the amphibole-bearing anorthite-clinopyroxene zone is a product of the reaction between mantle xenoliths and mafic magma. Plagioclase with high An value (92.0–99.95, average 97.79) indicates that the metasomatic melts have high Ca/Na and Al/Si ratios, possibly produced by the partial melting of ultra-depleted mantle under “wet” conditions. Combined with the data on other mantle xenoliths discovered in the NCC, our results suggest that the Mesozoic lithospheric mantle beneath the North Taihang Mountains within the central NCC is composed of ultra-depleted Archean and Paleoproterozoic peridotites and dunites modified by complex melts. We also propose that the destruction of eastern part of the NCC mainly occurred during Early Cretaceous, and that the boundary of the lithospheric destruction coincides with the Taihang Mountains.     

The influence of Al2O3 on the H2O content in periclase and ferropericlase at 25 GPa

In this paper I present results of IR spectroscopic measurements of water solubility in Al-bearing periclase and ferropericlase (Mg# = 88) synthesized at 25 GPa and 1400–2000 °C. The IR spectra of their crystals show narrow absorption peaks at 3299, 3308, and 3474 cm^?1. The calculated H₂O contents are 11–25 ppm in periclase (Al₂O₃ = 0.9–1.2 wt.%) and 14–79 ppm in ferropericlase (Al₂O₃ = 0.9–2.9 wt.%). Ferropericlase contains more H₂O and Al₂O₃ than periclase at 1800–2000 °C. I suggest that addition of Al₂O₃ does not influence the solubility of water in ferropericlase but can favor the additional incorporation of Fe₂O₃ into the structure. The incorporation of Fe³⁺ into ferropericlase increases water solubility as a result of iron reduction to Fe²⁺. It is shown that water has limited solubility in ferropericlase from mantle peridotite; therefore, ferropericlase cannot be considered an important hydrogen-bearing mineral in the lower mantle.     

Geodynamics of rapid voluminous felsic magmatism through time

Two end member geodynamic settings produce the observed examples of rapid voluminous felsic (rhyolitic) magmatism through time. The first is driven by mantle plume head arrival underneath a continent and has operated in an identifiable and regular manner since at least 2.45 Ga. This style produces high temperature (≤ 1100 °C), low aspect ratio rheoignimbrites and lavas that exhibit high SiO₂/Al₂O₃ ratios, high K₂O/Na₂O ratios, and where available data exists, high Ga/Al₂O₃ ratios (> 1.5) with high F (in thousands of parts per million) and low water content. F concentration is significant as it depolymerizes the silicate melt, influencing the magmas' physical behavior during development and emplacement. These rhyolites are erupted as part of rapidly emplaced (10–15 Myr) mafic LIPs and are formed primarily by efficient assimilation-fractional crystallization processes from a mafic mantle parent. The second is driven by lithospheric extension during continental rifting or back arc evolution and is exclusive to the Phanerozoic. SLIPs (silicic large igneous provinces) develop over periods < 40 Myr and manifest in elongate zones of magmatism that extend up to 2500 km, contrasting with the mafic LIP style. Some of the voluminous felsic magmas within SLIPs appear to have a very similar geochemistry and petrogenesis to that of the rhyolites within mafic LIPs. Other voluminous felsic magmas within SLIPs are sourced from hydrous lower crust, and contrast with those sourced from the mantle. They exhibit lower temperatures (< 900 °C), explosive ignimbrites with lower SiO₂/Al₂O₃ ratios, and lower K₂O/Na₂O ratios. Rapid voluminous felsic magmatism represents both extreme examples of continental growth since the Archean, and also dramatic periods of crustal recycling and maturation during the Phanerozoic.     

Nature and processes of the lithospheric mantle beneath the western Qinling: Evidence from deformed peridotitic xenoliths in Cenozoic kamafugite from Haoti,Gansu Province,China

The Cenozoic Haoti kamafugite field (23 Ma) is situated at the western Qinling Orogen, Gansu Province in China, which is a conjunction region of the North China Craton, the Yangtze Craton and the Tibetan Plateau. Fresh peridotitic xenoliths entrained in these volcanic rocks provide an opportunity to study the nature and processes of the lithospheric mantle beneath the western Qinling. These xenoliths can be divided into two groups based on the petrological features and mineral compositions, type 1 and type 2. Type 1 xenoliths with strongly deformed texture have higher Fo (90–92.5) contents in olivines, Mg# (91–94) and Cr# (15–35) of clinopyroxenes, and Cr# (36–67) of spinels than the weakly deformed type 2 xenoliths, which have the corresponding values of 89–90, 89–91.5, 10–15 and 5–15 in minerals, respectively. CaO contents in fine-grained olivines are slightly higher than 0.10 wt% compared with coarse-grained ones (less than 0.10 wt%). Fine-grained clinopyroxenes have low Al₂O₃ + CaO contents (generally <23 wt%) relative to coarse-grained ones (>23 wt%). Fo contents in fine-grained olivines mainly in the melt pocket of the type 1 xenoliths are higher than those in coarse-grained ones, which is somewhat contrary to the type 2 xenoliths without melt pocket. Clinopyroxenes of the type 2 display higher Na₂O contents (1.7–1.9 wt%) than those of the type 1 (<1.4 wt%). P–T estimations reveal that the type 1 xenoliths give temperature in range of 1106–1187 °C and pressure of 21–26 kbar and that relatively low temperature (907 and 1022 °C) and pressure (19.0 and 18.5 kbar) for the type 2 xenoliths. The type 1 xenoliths are characterized by depletion due to high degree of partial melting (>10%), modal metasomatic and deformed characteristics, and may represent the old refractory lithospheric mantle. In contrast, the type 2 peridotites show fertile features with low degree of partial melting (<5%) and may represent the newly-accreted lithospheric mantle. The lithospheric mantle beneath the western Qinling underwent partial melting, recrystallization, deformation and metasomatism due to asthenospheric upwelling and the latest decompression responding to the Cenozoic extensive tectonic environment. These processes perhaps are closely related to the evolution of Tibetan Plateau caused by the India-Asian collision.     

Post-collisional ultrapotassic rocks and mantle xenoliths in the Sailipu volcanic field of Lhasa terrane,south Tibet: Petrological and geochemical constraints on mantle source and geodynamic setting

Post-collisional ultrapotassic magmatic rocks (15.2–18.8 Ma), containing mantle xenoliths, are extensively distributed in the Sailipu volcanic field of the Lhasa terrane in south Tibet. They could be subdivided into high-MgO and low-MgO subgroups based on their petrological and geochemical characteristics. The high-MgO subgroup has olivine-I (Fo_87–92), phlogopite and clinopyroxene as phenocryst phases, while the low-MgO subgroup consists mainly of phlogopite, clinopyroxene and olivine-II (Fo_77–89). These ultrapotassic magmatic rocks have high MgO (4.6–14.5 wt%), Ni (145–346 ppm), Cr (289–610 ppm) contents, and display enrichment in light rare earth element (REE) over heavy REE and enriched large ion lithophile elements (LILE) relative to high field strength elements (HFSE) with strongly negative Nb-Ta-Ti anomalies in primitive mantle-normalized trace element diagrams. They have extremely radiogenic (⁸⁷Sr/⁸⁶Sr)_i (0.7167–0.7274) and unradiogenic (¹⁴³Nd/¹⁴⁴Nd)_i (0.5118–0.5120), high (²⁰⁷Pb/²⁰⁴Pb)_i (15.740–15.816) and (²⁰⁸Pb/²⁰⁴Pb)_i (39.661–39.827) at a given (²⁰⁶Pb/²⁰⁴Pb)_i (18.363–18.790) with high δ¹⁸O values (7.3–9.7‰). Strongly linear correlations between depleted mid-ocean ridge basalt-source mantle (DMM) and the Indian continental crust (HHCS) in Sr-Nd-Pb-O isotopic diagrams indicate that the geochemical features could result from reaction between mantle peridotite and enriched components (fluids and melts) released by the eclogitized Indian continental crust (HHCS) in the mantle wedge. The high-MgO (13.7–14.5 wt%) subgroup displays higher (¹⁴³Nd/¹⁴⁴Nd)_i, lower (⁸⁷Sr/⁸⁶Sr)_i and (²⁰⁶Pb/²⁰⁴Pb)_i ratios and lower δ¹⁸O values compared with the low-MgO (4.6–8.8 wt%) subgroup. High Ni (850–4862 ppm) contents of olivine phenocrysts and high whole-rock SiO₂, NiO, low CaO contents indicate that the low-MgO ultrapotassic magmatic rocks are derived from partial melting of olivine-poor mantle pyroxenite. However, lower Ni concentrations of olivine phenocryst and lower whole-rock SiO₂, NiO, higher CaO contents of the high-MgO ultrapotassic rocks may indicate their peridotite mantle source. This could be attributed to different amounts of silicate-rich components added into the mantle sources of the parental magmas in the mantle wedge caused by the northward subduction of the Indian continental lithosphere. The reaction-formed websterite xenoliths, reported for the first time in this study, are made up of anhedral and interlocking clinopyroxene (45–65 vol%) and orthopyroxene (30–50 vol%) with minor phlogopite (< 3 vol%) and quartz (< 2 vol%) and are suggested to be formed by silicate metasomatism of the mantle peridotite. The harzburgites, another major type of mantle xenolith in south Tibet, have a mineral assemblage of olivine (60–75 vol%), orthopyroxene (20–35 vol%), clinopyroxene (< 3 vol%), phlogopite (< 2 vol%) and spinel (< 2 vol%) and may have experienced subduction-related metasomatism. Combined with two types of ultrapotassic magmas, we propose that compositions of mantle wedge beneath south Tibet may gradually evolve from harzburgite through lherzolite to websterite with strong metasomatism of silicate-rich components in their mantle source region. Partial melting of the enriched mantle sources could be triggered by rollback of Indian continental slab during 25–8 Ma in south Tibet.     

Porphyry Cu (–Mo–Au) deposits related to melting of thickened mafic lower crust: Examples from the eastern Tethyan metallogenic domain

Most porphyry Cu deposits in the world occur in magmatic arc settings and are formed in association with calc-alkaline arc magmas related to subduction of oceanic lithosphere. This contribution reviews a number of significant porphyry Cu deposits in the eastern Tethyan metallogenic domain. They widely occur in a variety of non-arc settings, varying from post (late)-collisional transpressional and extensional environments to intracontinental extensional environments related to orogenic and anorogenic processes. Their spatial–temporal localization is controlled by strike–slip faults, orogen-transverse normal faults, lineaments and their intersections in these non-arc settings. These deposits are dominated by porphyry Cu–Mo deposits with minor porphyry Cu–Au and epithermal Au deposits, and exhibit a broad similarity with those in magmatic arcs. The associated magmas are generally hydrous, relatively high fO₂, high-K calc-alkaline and shoshonitic, and show geochemical affinity with adakites. They are distinguished from arc magmas and/or oceanic-slab derived adakites, by their occurrence as isolated complexes, high K₂O contents (1.2–8.5%), and much wider range of ε_Nd(t) values(? 10 to + 3) and positive ε_Hf(t) values (+ 4.6 to + 6.9). These potassic magmas are most likely formed by partial melting of thickened juvenile mafic lower-crust or delaminated lower crust, but also involving various amounts of asthenospheric mantle components. Key factors that generate hydrous fertile magmas are most likely crust/mantle interaction processes at the base of thickened lower-crust in non-arc settings, rather than oceanic-slab dehydration (as in arc settings). Breakdown of amphibole in thickened lower crust (e.g., amphibole eclogite and garnet amphibolite) during melting is considered to release fluids into the fertile magmas, leading to an elevated oxidation state and higher H₂O content necessary for development of porphyry Cu–Mo–Au systems. Copper and Au in hydrous magmas are likely derived from mantle-derived components and/or melts, which either previously underplated and infiltrated at the base of the thickened lower crust, or were input into the primitive magmas by melt/mantle interaction. In contrast, Mo and (part of the) S in the fertile magmas are probably supplied by old crust during melting and subsequent ascent.     

Source and H2O content of high-MgO magmas in island arc settings: an experimental study of a primitive calc-alkaline basalt from St. Vincent, lesser antilles arc

Liquidus phase relationships have been determined for a high-MgO basalt (STV301: MgO=12.5 wt%, Ni=250 ppm, Cr=728 ppm) from Black Point, St Vincent (Lesser Antilles arc). Piston-cylinder experiments were conducted between 7.5 and 20 kbar under both hydrous and oxidizing conditions. AuPd capsules were used as containers. Compositions of supraliquidus glasses and mass-balance calculations show that Fe loss is < 10% in the majority of experiments. Two series of water concentrations in melt were investigated: (i) 1.5 wt% and (ii) 4.5 wt% H₂O, as determined by SIMS analyses on quenched glasses and with the by difference technique. The Fe³⁺/Fe²⁺ partitioning between Cr-Al spinel and melt and olivine-spinel equilibria show that oxidizing fO₂ were imposed (NNO + 1.5 for the 1.5 wt% H₂O series, NNO + 2.3 for the 4.5 wt% H₂O series). For both series of water concentrations, the liquid is multiply-saturated with a spinel lherzolite phase assemblage on its liquidus, at 1235°C, 11.5 kbar (1.5 wt% H₂O) and 1185°C, 16 kbar (4.5 wt% H₂O). Liquidus phases are homogeneous and comparable to typical mantle compositions. Mineral-melt partition coefficients are generally identical to values under anhydrous conditions. The modal proportion cpx/opx on the liquidus decreases from the 1.5 wt% to the 4.5 wt% H₂O series. The experimental data are consistent with STV301 being a product of partial melting of lherzolitic mantle. Conditions of multiple saturation progressively evolve toward lower temperatures and higher pressures with increasing melt H₂O concentration. Phase equilibria constraints, i.e., the necessity of preserving the mantle signature seen in high-MgO and picritic arc basalts, and glass inclusion data suggest that STV301 was extracted relatively dry (∼ 2 wt% H₂O) from its mantle source. However, not all primary arc basalts are extracted under similarly dry conditions because more hydrous melts will crystallize during ascent and will not be present unmodified at the surface. From degrees of melting calculated from experiments on KLB-1, extraction of a 12.5 wt% MgO melt with ∼ 2 wt% H₂O would require a H₂O concentration of 0.3 wt% in the sub-arc mantle. For mantle sources fluxed with a slab-derived hydrous component, extracted melts may contain up to ∼ 5.5 wt% H₂O.     

Evidence of Mid-ocean ridge and shallow subduction forearc magmatism in the Nagaland-Manipur ophiolites,northeast India: constraints from mineralogy and geochemistry of gabbros and associated mafic dykes

We discuss here the mineralogical and geochemical characteristics of mafic intrusive rocks from the Nagaland-Manipur Ophiolites (NMO) of Indo-Myanmar Orogenic Belt, northeast India to define their mantle source and tectonic environment. Mafic intrusive sequence in the NMO is characterized by hornblende-free (type-I) and hornblende-bearing (type-II) rocks. The type-I is further categorized as mafic dykes (type-Ia) of tholeiitic N-MORB composition, having TiO₂ (0.72–1.93 wt.%) and flat REE patterns (La_N/Yb_N = 0.76–1.51) and as massive gabbros (type-Ib) that show alkaline E-MORB affinity, having moderate to high Ti content (TiO₂ = 1.18 to 1.45 wt.%) with strong LREE-HREE fractionations (La_N/Yb_N = 4.54–7.47). Such geochemical enrichment from N-MORB to E-MORB composition indicates mixing of melts derived from a depleted mantle and a fertile mantle/plume source at the spreading center. On the other hand, type-II mafic intrusives are hornblende bearing gabbros of SSZ-type tholeiitic composition with low Ti content (TiO₂ = 0.54 wt.%–0.86 wt.%) and depleted LREE pattern with respect to HREE (La_N/Yb_N = 0.37–0.49). They also have high Ba/Zr (1.13–2.82), Ba/Nb (45.56–151.66) and Ba/Th (84.58–744.19) and U/Th ratios (0.37–0.67) relative to the primitive mantle, which strongly represents the melt composition generated by partial melting of depleted lithospheric mantle wedge contaminated by hydrous fluids derived from subducting oceanic lithosphere in a forearc setting. Their subduction related origin is also supported by presence of calcium-rich plagioclase (An_16.6–32.3). Geothermometry calculation shows that the hornblende bearing (type-II) mafic rocks crystallized at temperature in range of 565°–625 °C ± 50 (at 10 kbar). Based on these available mineralogical and geochemical evidences, we conclude that mid ocean ridge (MOR) type mafic intrusive rocks from the NMO represent the section of older oceanic crust which was generated during the divergent process of the Indian plate from the Australian plate during Cretaceous period. Conversely, the hornblende-bearing gabbros (type-II) represent the younger oceanic crust which was formed at the forearc region by partial melting of the depleted mantle wedge slightly modified by the hydrous fluids released from the subducting oceanic slab during the initial stage of subduction of Indian plate beneath the Myanmar plate.     

Partial dehydration of brucite and its implications for water distribution in the subducting oceanic slab

Hydrous minerals within the subducting oceanic slab are important hosts for water. Clarification of the stability field of hydrous minerals helps to understand transport and distribution of water from the surface to the Earth’s interior. We investigated the stability of brucite, a prototype of hydrous minerals, by means of electrical conductivity measurements in both open and closed systems at 3 GPa and temperatures up to 1300 K. Dramatic increase of conductivity in association with characteristic impedance spectra suggests that partial dehydration of single-crystal brucite in the open system with a low water fugacity occurs at 950 K, which is about 300 K lower than those previously defined by phase equilibrium experiments in the closed system. By contrast, brucite completely dehydrates at 1300 K in the closed system, consistent with previous studies. Partial dehydration may generate a highly defective structure but does not lead to the breakdown of brucite to periclase and water immediately. Water activity plays a key role in the stability of hydrous minerals. Low water activity (aH₂O) caused by the high wetting behavior of the subducted oceanic slab at the transition zone depth may cause the partial dehydration of the dense hydrous magnesium silicates (DHMSs), which significantly reduces the temperature stability of DHMS (this mechanism has been confirmed by previous study on super hydrous phase B). As a result, the transition zone may serve as a ‘dead zone’ for DHMSs, and most water will be stored in wadsleyite and ringwoodite in the transition zone.     

Pressure-induced dehydration of dioptase: A single-crystal X-ray diffraction and Raman spectroscopy study

We present a synchrotron-based, single-crystal X-ray diffraction and Raman spectroscopy study of natural green dioptase (Cu₆Si₆O₁₈·6H₂O) up to ∼30 GPa at room temperature. The lattice parameters of dioptase exhibit continuous compression behavior up to ∼14.5 GPa, whereupon a structural transition is observed. Pressure–volume data below 14.5 GPa were fitted to a second-order Birch–Murnaghan equation of state with V₀ = 1440(2) ų and K₀ = 107(2) GPa, with K₀′ = 4(fixed). The low-pressure form of dioptase exhibits anisotropic compression with axial compressibility β_a > β_c in a ratio of 1.14:1.00. Based on the diffraction data and Raman spectroscopy, the new high-pressure phase could be regarded as a dehydrated form of dioptase in the same symmetry group. Pressure-induced dehydration of dioptase contributes broadly to our understanding of the high-pressure crystal chemistry of hydrous silicates containing molecular water groups.