Understanding the nature of parental melts for pyroxenite veins in supra-subduction zone(SSZ)ophiolites provides vibrant constraints on melt infiltration processes operating in subduction zones.The Zedang ophiolitic m...Understanding the nature of parental melts for pyroxenite veins in supra-subduction zone(SSZ)ophiolites provides vibrant constraints on melt infiltration processes operating in subduction zones.The Zedang ophiolitic massif in the eastern Yarlung–Zangbo suture zone in Tibet consists of mantle peridotites and a crustal section of gabbro,diabase,and basalt.Veins of two pyroxenite varieties cut the southern part of the Zedang massif.These pyroxenite rocks have different geochemical characteristics,where the first variety(type-I)has relatively higher contents of SiO_(2)(51.82–53.08 wt%),MgO(20.08–23.23 wt%),andΣPGE(3.42–13.97 ppb),and lower Al_(2)O_(3)(1.59–2.28 wt%)andΣREE(1.63–2.94 ppm).The second pyroxenite variety(type-II)is characterized by SiO_(2)(45.44–49.61 wt%),Mg O(16.68–19.78 wt%),Al_(2)O_(3)(4.24–8.77 wt%),ΣPGE(14.46–322.06 ppb),andΣREE(5.82–7.44 ppm).Pyroxenite type-I shows N-MORB-like chondritenormalized REE patterns.Zircon U-Pb ages of pyroxenite type-I(194±10 Ma),associated ophiolitic gabbro(135.3±2.0 Ma),and plagiogranite(124.2±2.3 Ma)evidently imply episodic evolution of the Zedang ophiolites.The mineralogical and geochemical characteristics of the investigated pyroxenites can be explained by subduction-initiated hydrous melting of metasomatized sub-arc mantle,later overprinted by sub-slab mantle melting triggered by upwelling asthenosphere during the Jurassic–Early Cretaceous times.The geochemical variations in pyroxenite vein composition,coupled with age differences amongst the other ophiolite units,may correspond to intermittent emplacement of pyroxenite dikes and isotropic gabbroic intrusions where the geodynamic setting progressed from arc maturation and slab rollback to slab tearing and delamination.展开更多
Pelletization of hematite ore requires high fineness and very high induration temperature（~1325 ℃） owing to its poor diffusion bonding unlike magnetite ore. Further, high-alumina hematite pellets show very high red...Pelletization of hematite ore requires high fineness and very high induration temperature（~1325 ℃） owing to its poor diffusion bonding unlike magnetite ore. Further, high-alumina hematite pellets show very high reduction degradation index（RDI） during low temperature（500-650 ℃） reduction due to their volume expansion and lattice distortion. Noamundi（India） hematite ore contains very high Al2O3（2.3%） with adverse ratio of alumina to silica（~2） for which, it shows very high RDI. In this work, the acid pellets prepared from Noamundi ore fines of optimum Blaine fineness show good cold crushing strength（CCS）. However, it shows very high RDI（77%）. In order to reduce RDI, Mg O in form of two different gangue-containing fluxes, such as pyroxenite and olivine in varying quantities has been added. The optimum requirement and performance of these fluxes has been examined and compared. Both pyroxenite and olivine fluxed pellets show significant lowering of RDI（26% and 23%, respectively） and improvement of other properties, viz CCS, swelling indices etc with good reducibility（70%-77%）. Finally, a good quality acidic hematite pellet was developed from high-alumina ore without using any lime which is very important charge material in combination of basic sinter in blast furnace.展开更多
Melting experiments on ultramafic rocks rich in the hydrous minerals phlogopite or phlogopite+K-rich terite,some including 5%of accessory phases,have been conducted at 15 and 50 kbar.The assemblages represent probable...Melting experiments on ultramafic rocks rich in the hydrous minerals phlogopite or phlogopite+K-rich terite,some including 5%of accessory phases,have been conducted at 15 and 50 kbar.The assemblages represent probable source components that contribute to melts in cratonic regions,but whose melt compositions are poorly known.A main series of starting compositions based on MARID xenoliths consisted of a third each of clinopyroxene(CPX),phlogopite(PHL)and K-richterite(KR)with or without 5%ilmenite,rutile or apatite.Additional experiments were run without KR and with higher proportions of accessory phases.Melt traps were used at near-solidus temperatures to facilitate accurate analysis of wellquenched melts,for which reversal experiments demonstrate equilibrium.Results show that KR melts rapidly and completely within 50°C of the solidus,so that melts reflect the composition of the amphibole and its melting reaction.Melts have high SiO_(2) and especially K_(2)O but low CaO and Al_(2)O_(3) relative to basaltic melts produced from peridotites at similar pressures.They have no counterparts amongst natural rocks,but most closely resemble leucite lamproites at 15 kbar.KR and PHL melt incongruently to form olivine(OL)and CPX at 15 kbar,promoting SiO2 contents of the melt,whereas orthopyroxene OPX is increasingly stable at lower lithosphere pressures,leading to an increase in Mg O and decrease in SiO_(2) in melts,which resemble olivine lamproites.Melts of mica pyroxenites without KR are richer in CaO and Al_(2)O_(3) and do not resemble lamproites.These experiments show that low CaO and Al_(2)O_(3) in igneous rocks is not necessarily a sign of a depleted peridotite source.Accessory phases produce melts exceptionally rich in P_(2)O_(5) or TiO_(2) depending on the phases present and are unlike any melts seen at the Earth’s surface,but may be important agents of metasomatism seen in xenoliths.The addition of the 5%accessory phases ilmenite,rutile or apatite result in melting temperatures a few ten of degrees lower;at least two of these appear essential to explain the compositions of many alkaline igneous rocks on cratons.Melting temperatures for CPX+PHL+KR mixtures are close to cratonic geotherms at depths>130 km:minor perturbations of the stable geotherm at>150 km will rapidly lead to 20%melting.Melts of hydrous pyroxenites with a variety of accessory phases will be common initial melts at depth,but will change if reaction with wall-rocks occurs,leading to volcanism that contains chemical components of peridotite even though the temperature in the source region remains well below the melting point of peridotite.At higher temperatures,extensive melting of peridotite will dilute the initial alkaline melts:this is recognizable as alkaline components in basalts and,in extreme cases,alkali picrites.Hydrous pyroxenites are,therefore,components of most mantle-derived igneous rocks:basaltic rocks should not be oversimplified as being purely melts of peridotite or of mixtures of peridotite and dry pyroxenite without hydrous phases.展开更多
Swarms of orthopyroxenite and websterite veins are found within Egiingol residual SSZ peridotite massif of Dzhida terrain(Central Asian Orogenic Belt,Northern Mongolia).The process of Egiingol pyroxenite veins formati...Swarms of orthopyroxenite and websterite veins are found within Egiingol residual SSZ peridotite massif of Dzhida terrain(Central Asian Orogenic Belt,Northern Mongolia).The process of Egiingol pyroxenite veins formation is investigated using new major and trace element analyses of pyroxenite minerals,calculations of closure temperatures and composition of equilibrium melt.The pyroxenites show abundant petrographic and geochemical evidence for replacement of the residual peridotite minerals by ortho-and clinopyroxene due to melt-rock interaction.Relics of peridotite olivines are found in pyroxenites,Cr#of spinel increases from peridotites to pyroxenites,and compositions of ortho-and clinopyroxene change from peridotite to pyroxenite.The authors show that calculated equilibrium melts for investigated pyroxenites are very similar to compositions of boninite lavas from the Dzhida terrain.Therefore,formation of pyroxenite veins most likely resulted from percolation of boninite melts through the Egiingol peridotites.Orthopyroxenite veins formed at first,followed by websterite veins.Thus,the authors assume that pyroxenite veins represent the channels for boninitic melts migration in supra-subduction environment.展开更多
Phlogopite-amphibole-pyroxenite xenoliths contained in the alkali basic-ultrabasic subvolcanic complex in Langao, Shaanxi Province, are composed of diopside, Ti-rich pargasite, phlogopite apatite, sphene and ilmenite,...Phlogopite-amphibole-pyroxenite xenoliths contained in the alkali basic-ultrabasic subvolcanic complex in Langao, Shaanxi Province, are composed of diopside, Ti-rich pargasite, phlogopite apatite, sphene and ilmenite, which have subsolidus metamorp hism- de formation textures such as triple-points, cataclastic boundaries and kink-bands. Mineral chemical characteristics show that the diopside, Ti-rich pargasite and phlogoPite are derived from the mantle and are the products of mantle metasomatism. Compared with normal mantle-derivedspinel-lherzolites, the xenoliths are enriched in TiO2, Fe2O3, CaO, Na2O and K2O, with apparent depletion in MgO. Chondrite-normalized REE patterns and primordial-mantle normalized trace elements data show that they are enriched in REE (especially LREE) and incompatible trace elements. The petrographic, mineralogical and petrochemical characteristics indicate that the xenoliths are metasomatized mantle xenoliths, which offers the evidence for mantle metasomatism and represents the anomalous mantle beneath the Early Paleozoic rift in northern Daba Mountains. The agents of mantle metasomatism are probably derived from the rising of mantle hot plumes. The processes of metasomatism varied from limited-range fluid metasomatism in deep mantle (＞90 km) to pervasive metasomatism of silicate melt.展开更多
The trace element compositions of melts and minerals from high-pressure experiments on hydrous pyroxenites containing K-richterite are presented. The experiments used mixtures of a third each of the natural minerals c...The trace element compositions of melts and minerals from high-pressure experiments on hydrous pyroxenites containing K-richterite are presented. The experiments used mixtures of a third each of the natural minerals clinopyroxene, phlogopite and K-richterite, some with the addition of 5% of an accessory phase ilmenite, rutile or apatite. Although the major element compositions of melts resemble natural lamproites, the trace element contents of most trace elements from the three-mineral mixture are much lower than in lamproites. Apatite is required in the source to provide high abundances of the rare earth elements, and either rutile and/or ilmenite is required to provide the high field strength elements Ti, Nb, Ta, Zr and Hf. Phlogopite controls the high levels of Rb, Cs and Ba.Since abundances of trace elements in the various starting mixtures vary strongly because of the use of natural minerals, we calculated mineral/melt partition coefficients (DMin/melt) using mineral modes and melting reactions and present trace element patterns for different degrees of partial melting of hydrous pyroxenites. Rb, Cs and Ba are compatible in phlogopite and the partition coefficient ratio phlogopite/K-richterite is high for Ba (136) and Rb (12). All melts have low contents of most of the first row transition elements, particularly Ni and Cu ((0.1-0.01)×primitive mantle). Nickel has high DMin/melt for all the major minerals (12 for K-richterite, 9.2 for phlogopite and 5.6 for Cpx) and so behaves at least as compatibly as in melting of peridotites. Fluorine/chlorine ratios in melts are high and DMin/melt for fluorine decreases in the order apatite (2.2) > phlogopite (1.5) > K-richterite (0.87). The requirement for apatite and at least one Ti-oxide in the source of natural lamproites holds for mica pyroxenites that lack K-richterite. The results are used to model isotopic ageing in hydrous pyroxenite source rocks: phlogopite controls Sr isotopes, so that lamproites with relatively low 87Sr/86Sr must come from phlogopite-poor source rocks, probably dominated by Cpx and K-richterite. At high pressures (>4 GPa), peritectic Cpx holds back Na, explaining the high K2O/Na2O of lamproites.展开更多
基金co-supported by Key Special Project for Introduced Talents Team of Southern Marine Science and Engineering Guangdong Laboratory(Guangzhou)(No.GML2019ZD0201)the Second Tibetan Plateau Scientific Expedition and Research Program(No.2019QZKK0801)+3 种基金the National Natural Science Foundation of China(NNSFCProject Nos.42272048,41720104009,42172069,92062215)the Key Laboratory of Deep-Earth Dynamics of Ministry of Natural Resources Fund(No.J1901-28)the China Geological Survey(CGS,Project Nos.DD20230340,DD20221630)。
文摘Understanding the nature of parental melts for pyroxenite veins in supra-subduction zone(SSZ)ophiolites provides vibrant constraints on melt infiltration processes operating in subduction zones.The Zedang ophiolitic massif in the eastern Yarlung–Zangbo suture zone in Tibet consists of mantle peridotites and a crustal section of gabbro,diabase,and basalt.Veins of two pyroxenite varieties cut the southern part of the Zedang massif.These pyroxenite rocks have different geochemical characteristics,where the first variety(type-I)has relatively higher contents of SiO_(2)(51.82–53.08 wt%),MgO(20.08–23.23 wt%),andΣPGE(3.42–13.97 ppb),and lower Al_(2)O_(3)(1.59–2.28 wt%)andΣREE(1.63–2.94 ppm).The second pyroxenite variety(type-II)is characterized by SiO_(2)(45.44–49.61 wt%),Mg O(16.68–19.78 wt%),Al_(2)O_(3)(4.24–8.77 wt%),ΣPGE(14.46–322.06 ppb),andΣREE(5.82–7.44 ppm).Pyroxenite type-I shows N-MORB-like chondritenormalized REE patterns.Zircon U-Pb ages of pyroxenite type-I(194±10 Ma),associated ophiolitic gabbro(135.3±2.0 Ma),and plagiogranite(124.2±2.3 Ma)evidently imply episodic evolution of the Zedang ophiolites.The mineralogical and geochemical characteristics of the investigated pyroxenites can be explained by subduction-initiated hydrous melting of metasomatized sub-arc mantle,later overprinted by sub-slab mantle melting triggered by upwelling asthenosphere during the Jurassic–Early Cretaceous times.The geochemical variations in pyroxenite vein composition,coupled with age differences amongst the other ophiolite units,may correspond to intermittent emplacement of pyroxenite dikes and isotropic gabbroic intrusions where the geodynamic setting progressed from arc maturation and slab rollback to slab tearing and delamination.
文摘Pelletization of hematite ore requires high fineness and very high induration temperature（~1325 ℃） owing to its poor diffusion bonding unlike magnetite ore. Further, high-alumina hematite pellets show very high reduction degradation index（RDI） during low temperature（500-650 ℃） reduction due to their volume expansion and lattice distortion. Noamundi（India） hematite ore contains very high Al2O3（2.3%） with adverse ratio of alumina to silica（~2） for which, it shows very high RDI. In this work, the acid pellets prepared from Noamundi ore fines of optimum Blaine fineness show good cold crushing strength（CCS）. However, it shows very high RDI（77%）. In order to reduce RDI, Mg O in form of two different gangue-containing fluxes, such as pyroxenite and olivine in varying quantities has been added. The optimum requirement and performance of these fluxes has been examined and compared. Both pyroxenite and olivine fluxed pellets show significant lowering of RDI（26% and 23%, respectively） and improvement of other properties, viz CCS, swelling indices etc with good reducibility（70%-77%）. Finally, a good quality acidic hematite pellet was developed from high-alumina ore without using any lime which is very important charge material in combination of basic sinter in blast furnace.
基金funded by grants from the Deutsche Forschungsgemeinschaft(Fo 181/3)the Australian Research Council(FL180100134)。
文摘Melting experiments on ultramafic rocks rich in the hydrous minerals phlogopite or phlogopite+K-rich terite,some including 5%of accessory phases,have been conducted at 15 and 50 kbar.The assemblages represent probable source components that contribute to melts in cratonic regions,but whose melt compositions are poorly known.A main series of starting compositions based on MARID xenoliths consisted of a third each of clinopyroxene(CPX),phlogopite(PHL)and K-richterite(KR)with or without 5%ilmenite,rutile or apatite.Additional experiments were run without KR and with higher proportions of accessory phases.Melt traps were used at near-solidus temperatures to facilitate accurate analysis of wellquenched melts,for which reversal experiments demonstrate equilibrium.Results show that KR melts rapidly and completely within 50°C of the solidus,so that melts reflect the composition of the amphibole and its melting reaction.Melts have high SiO_(2) and especially K_(2)O but low CaO and Al_(2)O_(3) relative to basaltic melts produced from peridotites at similar pressures.They have no counterparts amongst natural rocks,but most closely resemble leucite lamproites at 15 kbar.KR and PHL melt incongruently to form olivine(OL)and CPX at 15 kbar,promoting SiO2 contents of the melt,whereas orthopyroxene OPX is increasingly stable at lower lithosphere pressures,leading to an increase in Mg O and decrease in SiO_(2) in melts,which resemble olivine lamproites.Melts of mica pyroxenites without KR are richer in CaO and Al_(2)O_(3) and do not resemble lamproites.These experiments show that low CaO and Al_(2)O_(3) in igneous rocks is not necessarily a sign of a depleted peridotite source.Accessory phases produce melts exceptionally rich in P_(2)O_(5) or TiO_(2) depending on the phases present and are unlike any melts seen at the Earth’s surface,but may be important agents of metasomatism seen in xenoliths.The addition of the 5%accessory phases ilmenite,rutile or apatite result in melting temperatures a few ten of degrees lower;at least two of these appear essential to explain the compositions of many alkaline igneous rocks on cratons.Melting temperatures for CPX+PHL+KR mixtures are close to cratonic geotherms at depths>130 km:minor perturbations of the stable geotherm at>150 km will rapidly lead to 20%melting.Melts of hydrous pyroxenites with a variety of accessory phases will be common initial melts at depth,but will change if reaction with wall-rocks occurs,leading to volcanism that contains chemical components of peridotite even though the temperature in the source region remains well below the melting point of peridotite.At higher temperatures,extensive melting of peridotite will dilute the initial alkaline melts:this is recognizable as alkaline components in basalts and,in extreme cases,alkali picrites.Hydrous pyroxenites are,therefore,components of most mantle-derived igneous rocks:basaltic rocks should not be oversimplified as being purely melts of peridotite or of mixtures of peridotite and dry pyroxenite without hydrous phases.
基金The reported study was funded by RFBR according to the research project(18-35-00535)IGC State Assignment Project(0350-2019-0008).
文摘Swarms of orthopyroxenite and websterite veins are found within Egiingol residual SSZ peridotite massif of Dzhida terrain(Central Asian Orogenic Belt,Northern Mongolia).The process of Egiingol pyroxenite veins formation is investigated using new major and trace element analyses of pyroxenite minerals,calculations of closure temperatures and composition of equilibrium melt.The pyroxenites show abundant petrographic and geochemical evidence for replacement of the residual peridotite minerals by ortho-and clinopyroxene due to melt-rock interaction.Relics of peridotite olivines are found in pyroxenites,Cr#of spinel increases from peridotites to pyroxenites,and compositions of ortho-and clinopyroxene change from peridotite to pyroxenite.The authors show that calculated equilibrium melts for investigated pyroxenites are very similar to compositions of boninite lavas from the Dzhida terrain.Therefore,formation of pyroxenite veins most likely resulted from percolation of boninite melts through the Egiingol peridotites.Orthopyroxenite veins formed at first,followed by websterite veins.Thus,the authors assume that pyroxenite veins represent the channels for boninitic melts migration in supra-subduction environment.
文摘Phlogopite-amphibole-pyroxenite xenoliths contained in the alkali basic-ultrabasic subvolcanic complex in Langao, Shaanxi Province, are composed of diopside, Ti-rich pargasite, phlogopite apatite, sphene and ilmenite, which have subsolidus metamorp hism- de formation textures such as triple-points, cataclastic boundaries and kink-bands. Mineral chemical characteristics show that the diopside, Ti-rich pargasite and phlogoPite are derived from the mantle and are the products of mantle metasomatism. Compared with normal mantle-derivedspinel-lherzolites, the xenoliths are enriched in TiO2, Fe2O3, CaO, Na2O and K2O, with apparent depletion in MgO. Chondrite-normalized REE patterns and primordial-mantle normalized trace elements data show that they are enriched in REE (especially LREE) and incompatible trace elements. The petrographic, mineralogical and petrochemical characteristics indicate that the xenoliths are metasomatized mantle xenoliths, which offers the evidence for mantle metasomatism and represents the anomalous mantle beneath the Early Paleozoic rift in northern Daba Mountains. The agents of mantle metasomatism are probably derived from the rising of mantle hot plumes. The processes of metasomatism varied from limited-range fluid metasomatism in deep mantle (＞90 km) to pervasive metasomatism of silicate melt.
基金funded by grants from the Deutsche Forschungsgemeinschaft,Germany (Fo 181/3)and the Australian Research Council,Australia (FL180100134).
文摘The trace element compositions of melts and minerals from high-pressure experiments on hydrous pyroxenites containing K-richterite are presented. The experiments used mixtures of a third each of the natural minerals clinopyroxene, phlogopite and K-richterite, some with the addition of 5% of an accessory phase ilmenite, rutile or apatite. Although the major element compositions of melts resemble natural lamproites, the trace element contents of most trace elements from the three-mineral mixture are much lower than in lamproites. Apatite is required in the source to provide high abundances of the rare earth elements, and either rutile and/or ilmenite is required to provide the high field strength elements Ti, Nb, Ta, Zr and Hf. Phlogopite controls the high levels of Rb, Cs and Ba.Since abundances of trace elements in the various starting mixtures vary strongly because of the use of natural minerals, we calculated mineral/melt partition coefficients (DMin/melt) using mineral modes and melting reactions and present trace element patterns for different degrees of partial melting of hydrous pyroxenites. Rb, Cs and Ba are compatible in phlogopite and the partition coefficient ratio phlogopite/K-richterite is high for Ba (136) and Rb (12). All melts have low contents of most of the first row transition elements, particularly Ni and Cu ((0.1-0.01)×primitive mantle). Nickel has high DMin/melt for all the major minerals (12 for K-richterite, 9.2 for phlogopite and 5.6 for Cpx) and so behaves at least as compatibly as in melting of peridotites. Fluorine/chlorine ratios in melts are high and DMin/melt for fluorine decreases in the order apatite (2.2) > phlogopite (1.5) > K-richterite (0.87). The requirement for apatite and at least one Ti-oxide in the source of natural lamproites holds for mica pyroxenites that lack K-richterite. The results are used to model isotopic ageing in hydrous pyroxenite source rocks: phlogopite controls Sr isotopes, so that lamproites with relatively low 87Sr/86Sr must come from phlogopite-poor source rocks, probably dominated by Cpx and K-richterite. At high pressures (>4 GPa), peritectic Cpx holds back Na, explaining the high K2O/Na2O of lamproites.
