俄罗斯Kurile-Kamchatka地区安山质熔体的成分、挥发分组成和微量元素

Melt inclusions in minerals from some volcanoes of the Kurile-Kamchatka region were examined.The studied basaltic andesites and andesites were sampled from volcanoes of the Central Kamchatka depression(Shiveluch and Bezymyannyi),Eastern Kamchatka volcanic belt(Avachinskii and Karymskii),and Iturup Island,Southern Kuriles(Kudryavyi).Basalts of the 1996 eruption of the Karymskii volcanic center and dacites of Dikii Greben'volcano,Southern Kamchatka were also studied.More than 260 melt inclusions from 31 rock samples were homogenized,and quenched glasses were analyzed using electron and ion microprobes.The compositions of melt inclusions in andesitic phenoerysts vary in silica contents from 56 to 80wt%.Al_2 O_3 ,FeO,MgO,CaO decrease and Na_2O and K_2O increase with increasing SiO_2.Many inclusions(about 80% )are dacitic or rhyolitic.However,the compositions of silicic glasses(>65wt% SiO_2)in andesites significantly differ in TiO2,FeO,MgO,CaO,and K_2O contents from those in dacites and rhyolites.High-potassium melts(K_2O 3.8～6.8wt% )with various SiO_2 from 51.4 to 77.2wt% were found in minerals of all volcanoes studied.This indicates a contribution of a component selectively enriched in potassium to magmas of the whole region.A great compositional diversity of melt inclusions in plagioelase phenocrysts from the Bezymyannyi andesites suggests a complex history of plagioclase crystallization and magma evolution in the andesite formation.Melts from different volcanoes strongly vary in volatile contents.The highest H_2O contents are found in the melts from Shiveluch(3.0～7.2wt%,4.7wt% on average)and Avachinskii (4.7～4.8wt%);while those are lower in melts of Kudryavyi(0.1～2.6wt% ),Dikii Greben'(0.4～1.8wt%),and Bezymyannyi (<1wt%).Chlorine contents are also variable.The lowest values are found in the Bezymyannyi melts(0.09wt% on average),the highest Cl contents are typical of melt inclusions in minerals from the Karymskii andesites(0.26wt% on average).The melts from Avachinskii,Dikii Greben',Kudryavyi,and Shiveluch show intermediate Cl contents(0.13～0.20wt% ).The pressure of 350～1600 bar determined by CO_2 fluid inclusions in plagioclase from the Shiveluch andesites suggests a magma chamber at a depth of 1.5～6 km. Concentrations of 17 elements were determined in glasses of melt inclusions in plagioclases from five volcanoes(Avachinskii, Bezymyannyi,Dikii Greben',Kudryavyi,and Shiveluch).The studied melts show similar trace-element patterns with Nb and Ti minima and B,K,Be,and Li maxima.The melts are close to typical island arc magmas by Sr/Y,La/Yb,K/Ti,and Ca/St ratios, and have some specific regional geochemical features.REE patterns sensitive to degree of magma differentiation indicate that Kudryavyi magmas are most primitive,while Shiveluch magmas are most evolved.     

俄罗斯Chukchi半岛新生代碱性岩的形成和演化：熔体和流体包裹体证据

Melt and fluid inclusions were studied in the minerals of Cenozoic olivine melanephelinites from the Chukchi Peninsula, Russia.The rock contain several generations of olivine phenocrysts varying in composition at mg=0.88～0.77.The phenocrysts bear fluid and melt inclusions recording various stages of melt crystallization in volcanic conduits and shallow magma chambers.Primary fluid inclusions are CO_2-dominated with a density of up to O.93 g/cm~3.All fluid inclusions are partially leaked,which is indicated by haloes of tiny fluid bubbles around large fluid inclusions in minerals.Melt inclusions contain various daughter crystals,which were completely resorbed in thermometric experiments at about 1230℃.Assuming that this temperature corresponds to the entrapment conditions of the CO_2 fluid inclusions,the minimum pressure of the beginning of magma degassing is estimated as 800MPa.Variations in the compositions of homogenized silicate melt inclusions indicate that olivine was the earliest crystalline phase followed by clinopyroxene,nepheline and orthoclase.This sequence is in agreement with the mineralogy of the rocks.The melts are strongly enriched in incompatible trace elements and volatiles(in addition to CO_2,high C1,F,and S contents were detected).There are some differences between the compositions of melts trapped in minerals from different samples.Variations in SiO_2,FeO,and incompatible element contents are probably related to melt generations at various levels in a homogeneous mantle reservoir.     

Study on the Physical and Chemical Conditions of Ore Formation of Hetai Ductile Shear Zone—Hosted Gold Deposit and Discovery of Melt Inclusions

The Hetai ductile shear zone-hosted gold deposit occurs in the deep-seated fault mylonite zone of the Sinian-Silurian metamorphic rock series. In this study there have been discovered melt inclusions, fluid-melt inclusions and organic inclusions in ore-bearing quartz veins of the ore deposit and mylonite for the first time. The homogenization temperatures of the various types of inclusions are 160℃, 180 - 350℃, 530℃ and 870℃ for organic inclusions, liquid inclusions, two-phase immiscible liquid inclusions and melt inclusions, respectively. Ore fluid is categorized as the neutral to basic K+ -Ca2+ -Mg2+ -Na+ - SO2- 4-HCO3-Cl- system. The contents of trace gases follow a descending order of H2O＞CO2＞CH4＞(or ＜ ) H2＞CO＞C2H2＞C2I-I6＞O2＞N2.The concentrations of K , Ca2 + ,SO2-4,HCO3-,Cl- H2O and C2H2 in fluid inclusions are related to the contents of gold and the Au/Ag ratios in ores from different levels of the gold deposit. This is significant for deep ore prospecting in the region. Daughter minerals in melt inclusions were analyzed using SEM. Quartz, orthoclase, wollastonite and other silicate minerals were identified. They were formed in different mineral assemblages.This analysis further proves the existence of melt inclusions in ore veins. Sedimentary metamorphic rocks could form silicate melts during metamorphic anatexis and dynamic metamorphism, which possess melt-solution characteristics. Ore formation is related to the multi-stage forming process of silicate melt and fluid.     

Hydromagmatic amphibole in komatiitic, tholeiitic and ferropicritic units, Abitibi greenstone belt, Ontario and Québec: evidence for Archaean wet basic and ultrabasic melts

Summary ?Detailed petrographic, electron microprobe and ion probe studies of Archaean hydromagmatic amphiboles from the Abitibi greenstone belt, Canada, yield new insights into the origin of Al-undepleted komatiitic and Al-depleted tholeiitic and ferropicritic melts. The amphiboles are present in peridotite layers and basal chill zones of thick differentiated basic and ultrabasic sills and flows, and are titanian pargasite–hastingsite in composition. They can be grouped into two petrographic types: (1) amphibole in the groundmass; and (2) amphibole-bearing melt inclusions. The groundmass amphiboles are oikocrysts, rims and interstitial grains, present in minor to major amounts. The oikocrysts host cumulus olivines (Fo_83–84) that are rounded in shape, embayed, and smaller in size. The amphibole-bearing melt inclusions are hosted in cumulus olivines (Fo_83–84 in komatiitic rocks and Fo₇₉ in tholeiitic rocks), spherical to ovoid in shape, 50–500 μm in size, and dominated modally by amphibole. The melt inclusions also contain euhedral chromite and aluminous spinel and micrometric clinopyroxene and glass, and sub-micrometric iron–nickel sulphide, chloro-apatite and ilmenite. In-situ ion probe analyses indicate the amphibole is: (1) enriched in Nb, LREE and Zr and depleted in Sr and HREE relative to primitive mantle; (2) contains up to 1–3 wt% H₂O; and (3) overall displays δD values from 50‰ to −140‰, including many values in the accepted magmatic range of −60‰ to −90‰. The petrographic relationships and geochemical compositions, and comparisons to experimental systems, indicate amphibole formation by subsolidus reaction of residual hydrous silicate melt with olivine and clinopyroxene. Some of the hydrous melt intruded and was entrapped as secondary melt inclusions within relict olivine. Rapid crystallization of the hydrous melt inclusions formed amphibole+clinopyroxene±glass±spinel or solely glass. Bulk compositions of the melt inclusions, comparisons to experimental phase equilibria, and presence of magmatic water suggest amphibole crystallisation from olivine → pyroxene residual melts with at least 2–3 wt% H₂O during rapid solidification of the host units. Adjustment for anhydrous phase crystallization (mainly olivine) suggests the initial melts contained 1–2 wt% H₂O. Such high H₂O contents and the magmatic δD compositions are consistent with the participation of H₂O in melt petrogenesis. However, most Abitibi komatiites and tholeiites lack hydromagmatic minerals, making it difficult to attribute all basic and ultrabasic melts to melting in hydrous Archaean mantle. The favoured model is that some Abitibi basic and ultrabasic melts were wet and some were dry, as well as Al-depleted or Al-undepleted. Received July 24, 2001; revised version accepted January 9, 2002     

The role of carbonate-fluoride melt immiscibility in shallow REE deposit evolution

The Lugiin Gol nepheline syenite intrusion, Mongolia, hosts a range of carbonatite dikes mineralized in rare-earth elements(REE). Both carbonatites and nepheline syenite-fluorite-calcite veinlets are host to a previously unreported macroscale texture involving pseudo-graphic intergrowths of fluorite and calcite. The inclusions within calcite occur as either pure fluorite, with associated REE minerals within the surrounding calcite, or as mixed calcite-fluorite inclusions, with associated zirconosilicate minerals. Consideration of the nature of the texture, and the proportions of fluorite and calcite present(～29 and 71 mol%,respectively), indicates that these textures most likely formed either through the immiscible separation of carbonate and fluoride melts, or from cotectic crystallization of a carbonatefluoride melt. Laser ablation ICP-MS analyses show the pure fluorite inclusions to be depleted in REE relative to the calcite. A model is proposed, in which a carbonate-fluoride melt phase enriched in Zr and the REE, separated from a phonolitic melt, and then either unmixed or underwent cotectic crystallization to generate an REE-rich carbonate melt and an REE-poor fluoride phase. The separation of the fluoride phase(either solid or melt) may have contributed to the enrichment of the carbonate melt in REE, and ultimately its saturation with REE minerals. Previous data have suggested that carbonate melts separated from silicate melts are relatively depleted in the REE, and thus melt immiscibility cannot result in the formation of REE-enriched carbonatites. The observations presented here provide a mechanism by which this could occur, as under either model the textures imply initial separation of a mixed carbonate-fluoride melt from a silicate magma. The separation of an REEenriched carbonate-fluoride melt from phonolitic magma is a hitherto unrecognized mechanism for REE-enrichment in carbonatites, and may play an important role in the formation of shallow magmatic REE deposits.     

中国山东昌乐地区碱性玄武岩刚玉中记录的岩浆不混溶作用

Abundant melt-and fluid inclusions occur in corundum megacrysts of alkaline basalt from the Changle area,Shandong province,eastern China.One type of melt inclusions,i.e.muhiphase melt inclusions(glass bubbles daughter minerals)were identified,which occur along growth zones of host corundum megacrysts.Microthermometry and laser Raman microprobe analysis were performed on the melt inclusions.The bubbles within the melt inclusions are confirmed to be CO_2-rich phase and the daughter minerals are probably silicates,such as augite and okenite.The results of high temperature homogenization experiment strongly suggest that two immiscible melts,i.e.a H_2O-and CO_2-rich melt and an anhydrous and CO_2-poor melt were trapped by melt inclusions in corundum megacryst.     

中国吉林长白山地区地幔捕虏体中硫化物熔体包裹体

Mantle xenoliths are common in the Cenozoic basalts of the Changbaishan District,Jilin Province,China.Sulfide assemblages in mantle minerals can be divided into three types:isolated sulfide grains,sulfide-meh inclusions and filling sulfides in fractures.Sulfide-meh inclusions occur as single-phase sulfides,sulfide-silicate melt,and CO_2-sulfide-silicate melt inclusions. Isolated sulfide grains are mainly composed of pyrrhotite,but cubanite was found occasionally.Sulfide-meh inclusions are mainly composed of pontlandite and MSS,with small amounts of chalcopyrite and talnakhite.The calculated distribution coefficient K_(D3)for lherzolite are similar to that of mean experimental value.The bulk sulfides in lherzolite were in equilibrium with the enclosing minerals, indicating immiscible sulfide melts captured in partial melting of upper mantle.Sulfide in fractures has higher Ni/Fe and(Fe Ni)/S than those of sulfide melt inclusions.They might represent later metasomatizing fluids in the mantle.Ni/Fe and(Fe Ni)/S increase from isolated grains,sulfide inclusions to sulfides in fractures.These changes were not only affected by temperature and pressure,hut by geochemistry of Ni,Fe and Cu,and sulfur fugacity as well.     

Mineral Inclusions in Chromite from the Chromite Deposit in the Kudi Ophiolite, Tibet, Proto-Tethys

High-Al chromite from the Kudi chromitites contains a wide range of mineral inclusions. They include clinopyroxene, amphibole, phlogopite, olivine, orthopyroxene, apatite, base-metal sulfides, calcite and brucite. The modal abundance of inclusions vary greatly among different grains of chromite. The common inclusions are clinopyroxene and amphibole, which occur as monomineral or polymineral associated with other minerals. The shapes of these inclusions tend to follow the growth plane of host chromite. Mineral assemblages and textures demonstrate that some inclusions(olivine, clinopyroxene) are trapped during magmatic stage, and most of the inclusions(e.g., amphibole, phlogopite) are trapped during recrystallization of chromite. Sulfide inclusions are pentlandite, chalcopyrite and cubanite. They occur either as isolated grains or together with silicate minerals, and formed from the separation of sulfide-bearing liquid from silicate magma. The parental magma of chromitites contains Al_2O_3 15.0wt%–16.5wt%, TiO_20.30wt%–1.05wt% based on calculation with the composition of chromite, similar to parental magma of high-Al chromitites from elsewhere and the estimated melt composition is comparable with that of MORB. Considering the high-Mg olivine in disseminated chromitite and abundant hydrous inclusions, we propose that Kudi chromitites formed beneath a volcanic front during the subduction initiation of Proto-Tethys.     

Trace Elements of Multi-stage Minerals and Titanite U-Pb Dating for the Gneisses from Liansan Island, Sulu UHPM Belt

Gneisses with anatectic characteristics from the Liansan island in the Sulu UHPM (ultra-high pressure metamorphic) belt were studied for petrography, titanite U-Pb dating and mineral geochemistry. Three origins of garnets are distinguished: metamorphic garnet, peritectic garnet and anatectic garnet, which are formed in the stages of peak metamorphism, retrograde anatexis and melt crystallization, respectively. The euhedral titanite has a high content of REE and high Th/U ratios, which is interpreted as indicating that it was newly-formed from an anatectic melt. The LA-ICP-MS titanite U-Pb dating yields 214–217 Ma ages for the titanite (melt) crystallization. The distribution of trace elements varies in response to the different host minerals at different stages. At the peak metamorphic stage, Y and HREE are mainly hosted by garnet, Ba and Rb by phengite, Sr, Nb, Ta, Pb, Th, U and LREE by allanite and Y, U and HREE by zircon. During partial melting, Y, Pb, Th, U and REE are released into the melt, which causes a dramatic decline of these element contents in the retrograde minerals. Finally, titanite absorbs most of the Nb, U, LREE and HREE from the melt. Therefore, the different stages of metamorphism have different mineral assemblages, which host different trace elements.     

The Genesis and Evolution of Alpine-Type Ultrabasic Rocks in Western Junggar, Xinjiang

The alpine-type ultrabasic rocks of the studied area have undergone plastic deformation under a temperature about 800--1200℃, a pressure about 0.9--1.68 GPa and differential stress of 0.2--0.35 GPa in relatively dry conditions, forming ultrabasie mylonite with porphyroclastic and mylonitic textures, Primary crystallized silicate melt inclusions and melt-fluid inclusions are discovered in porphyroclastic minerals and ore-forming chrome spinel. These rocks are formed under relatively stable physico-chemical conditions through liquid immiscibility of silicate melts, at 1200°-- 1300° and 1.1--1.38 GPa, equivalent to a depth of 40--50 km. No inclusion has been found in recrystallized secondary olivine and pyroxene, indicating that the plastic deformation happened after the formation of the rocks.     

Multiphase carbonate-salt immiscibility in carbonatite melts: data on melt inclusions from the Krestovskiy massif minerals (Polar Siberia)

Minerals of olivine–melilite and olivine–monticellite rocks from the Krestovskiy massif contain primary silicate-salt, carbonate-salt, and salt melt inclusions. Silicate-salt inclusions are present in perovskite I and melilite. Thermometric experiments conducted on these inclusions at 1,230–1,250°C showed silicate–carbonate liquid immiscibility. Globules of composite carbonate-salt melt rich in alkalies, P, S, and Cl separated in silicate melt. Carbonate salt globules in some inclusions from perovskite II at 1,190–1,200°C separated into immiscible liquid phases of simpler composition. Carbonate-salt and salt inclusions occur in monticellite, melilite, and garnet and homogenize at close temperatures (980–780°C). They contain alkalies, Ca, P, SO₃, Cl, and CO₂. According to the ratio of these components and predominance of one of them, melt inclusions are divided into 6 types: I—hyperalkaline (CaO/(Na₂O+K₂O)≤1) carbonate melts; II—moderately alkaline (CaO/(Na₂O+K₂O)>1) carbonate melts; III—sulfate-alkaline melts; IV—phosphate-alkaline melts; V—alkali-chloridic melts, and VI—calc-carbonate melts. Joint occurrence of all the above types and their syngenetic character were established. Some inclusions demonstrated carbonate-salt immiscibility phenomena at 840–800°C. A conclusion in made that the origin of carbonate melts during the formation of intrusion rocks is related to silicate–carbonate immiscibility in parental alkali-ultrabasic magma. The separated carbonate melt had a complex alkaline composition. Under unstable conditions the melt began to decompose into simpler immiscible fractions. Different types of carbonate-salt and salt inclusions seem to reflect the composition of these spatially isolated immiscible fractions. Liquid carbonate-salt immiscibility took place in a wide temperature range from 1,200–1,190°C to 800°C. The occurrence of this kind of processes under macroconditions might, most likely, cause the appearance of different types of immiscible carbonate-salt melts and lead to the formation of different types of carbonatites: alkali-phosphatic, alkali-sulfatic, alkali-chloridic, and, most widespread, calcitic ones.     

Carbonatite melts and genesis of apatite mineralization in the Guli pluton (northern East Siberia)

Inclusions of mineral-forming environments in apatite-containing ijolites and magnetite–phlogopite–apatite ores in carbonatites were studied to elucidate the genesis of apatite mineralization in the Guli alkaline ultramafic carbonatite massif. Primary inclusions of carbonate–salt and carbonate melts have been discovered and studied. The carbonate–salt melt inclusions are of alkaline high-Ca composition and are enriched in P, Sr, SO₃, and F (wt.%): CaO—30–40, Na₂O—5–12, K₂O—2–4, P₂O₅—1–3, SO₃—1.5–3, and SrO—1–3. They also contain minor MgO, FeO, BaO, and SiO₂ (tenths and hundredths of percent). The homogenization temperature of these inclusions is 850–970 °C. The carbonate inclusions contain predominant CaO (54–67 wt.%) and minor MgO, FeO, SrO, Na₂O, and P₂O₅ (tenths of percent). Their homogenization temperature is 840–860 °C. Similar primary carbonate–salt and carbonate inclusions were found in garnet, and secondary ones were detected in silicate minerals (clinopyroxene and nepheline) of ijolites. Clinopyroxenes of ijolites also contain primary inclusions of alkaline ultramafic high-Ca melts similar in composition to melilitite-melanephelinites highly enriched in P, SO₃, and CO₂ (wt.%): SiO₂—41–46, Al₂O₃—8–16, FeO—2–8, MgO—3–6, CaO—12–20, Na₂O—2–9, K₂O—1–6, P₂O₅—0.4–2.1, SO₃—0.2–2.3, and Cl—0.02–0.35. According to the obtained data, apatite of the magnetite–phlogopite–apatite ores and ijolites of the Guli pluton crystallized from phosphorus-rich alkaline carbonate–salt melts at 850–970 °C. The generation of these melts was, most likely, due to the silicate–salt immiscibility in melilitite-melanephelinite melts highly enriched in salts, which occurred either at the final stages of clinopyroxene crystallization or during the formation of melilite. The presence of alkalies, S, F, and CO₂ in spatially separated carbonate–salt melts contributed to the concentration and preservation of phosphorus in them at low temperatures, which led to the formation of apatite mineralization in ijolites and ore deposit in carbonatites.© 2015, V.S. Sobolev IGM, Siberian Branch of the RAS. Published by Elsevier B.V. All rights reserved.     

Geochemical evolution of halogen-enriched granite magmas and mineralizing fluids of the Zinnwald tin-tungsten mining district,Erzgebirge, Germany

We remelted and analyzed crystallized silicate melt inclusions in quartz from a porphyritic albite-zinnwaldite microgranite dike to determine the composition of highly evolved, shallowly intruded, Li- and F-rich granitic magma and to investigate the role of crystal fractionation and aqueous fluid exsolution in causing the extreme extent of magma differentiation. This dike is intimately associated with tin- and tungsten-mineralized granites of Zinnwald, Erzgebirge, Germany. Prior research on Zinnwald granite geochemistry was limited by the effects of strong and pervasive greisenization and alkali-feldspar metasomatism of the rocks. These melt inclusions, however, provide important new constraints on magmatic and mineralizing processes in Zinnwald magmas.The mildly peraluminous granitic melt inclusions are strongly depleted in CAFEMIC constituents (e.g., CaO, FeO, MgO, TiO₂), highly enriched in lithophile trace elements, and highly but variably enriched in F and Cl. The melt inclusions contain up to several thousand ppm Cl and nearly 3 wt% F, on average; several inclusions contain more than 5 wt% F. The melt inclusions are geochemically similar to the corresponding whole-rock sample, except that the former contain much more F and less CaO, FeO, Zr, Nb, Sr, and Ba. The Sr and Ba abundances are very low implying the melt inclusions represent magma that was more evolved than that represented by the bulk rock. Relationships involving melt constituents reflect increasing lithophile-element and halogen abundances in residual melt with progressive magma differentiation. Modeling demonstrates that differentiation was dominated by crystal fractionation involving quartz and feldspar and significant quantities of topaz and F-rich zinnwaldite. The computed abundances of the latter phases greatly exceed their abundances in the rocks, suggesting that the residual melt was separated physically from phenocrysts during magma movement and evolution.Interactions of aqueous fluids with silicate melt were also critical to magma evolution. To better understand the role of halogen-charged, aqueous fluids in magmatic differentiation and in subsequent mineralization and metasomatism of the Zinnwald granites, Cl-partitioning experiments were conducted with a F-enriched silicate melt and aqueous fluids at 2,000 bar (200 MPa). The results of the experimentally determined partition coefficients for Cl and F, the compositions of fluid inclusions in quartz and other phenocrysts, and associated geochemical modeling point to an important role of magmatic-hydrothermal fluids in influencing magma geochemistry and evolution. The exsolution of halogen-charged fluids from the Li- and F-enriched Zinnwald granitic magma modified the Cl, alkali, and F contents of the residual melt, and may have also sequestered Li, Sn, and W from the melt. Many of these fluids contained strongly elevated F concentrations that were equivalent to or greater than their Cl abundances. The exsolution of F-, Cl-, Li-, ± W- and Sn-bearing hydrothermal fluids from Zinnwald granite magmas was important in effecting the greisenizing and alkali-feldspathizing metasomatism of the granites and the concomitant mineralization.Editorial Handling: B. Lehmann     

Mineral/melt partitioning of trace elements during hydrous peridotite partial melting

This experimental study examines the mineral/melt partitioning of incompatible trace elements among high-Ca clinopyroxene, garnet, and hydrous silicate melt at upper mantle pressure and temperature conditions. Experiments were performed at pressures of 1.2 and 1.6 GPa and temperatures of 1,185 to 1,370 °C. Experimentally produced silicate melts contain up to 6.3 wt% dissolved H ₂O, and are saturated with an upper mantle peridotite mineral assemblage of olivine+orthopyroxene+clinopyroxene+spinel or garnet. Clinopyroxene/melt and garnet/melt partition coefficients were measured for Li, B, K, Sr, Y, Zr, Nb, and select rare earth elements by secondary ion mass spectrometry. A comparison of our experimental results for trivalent cations (REEs and Y) with the results from calculations carried out using the Wood-Blundy partitioning model indicates that H ₂O dissolved in the silicate melt has a discernible effect on trace element partitioning. Experiments carried out at 1.2 GPa, 1,315 °C and 1.6 GPa, 1,370 °C produced clinopyroxene containing 15.0 and 13.9 wt% CaO, respectively, coexisting with silicate melts containing ~1–2 wt% H ₂O. Partition coefficients measured in these experiments are consistent with the Wood-Blundy model. However, partition coefficients determined in an experiment carried out at 1.2 GPa and 1,185 °C, which produced clinopyroxene containing 19.3 wt% CaO coexisting with a high-H ₂O (6.26±0.10 wt%) silicate melt, are significantly smaller than predicted by the Wood-Blundy model. Accounting for the depolymerized structure of the H ₂O-rich melt eliminates the mismatch between experimental result and model prediction. Therefore, the increased Ca ²⁺ content of clinopyroxene at low-temperature, hydrous conditions does not enhance compatibility to the extent indicated by results from anhydrous experiments, and models used to predict mineral/melt partition coefficients during hydrous peridotite partial melting in the sub-arc mantle must take into account the effects of H ₂O on the structure of silicate melts.     

Anatexis and fluid regime of the deep continental crust: New clues from melt and fluid inclusions in metapelitic migmatites from Ivrea Zone (NW Italy)

We investigate the inclusions hosted in peritectic garnet from metapelitic migmatites of the Kinzigite Formation (Ivrea Zone, NW Italy) to evaluate the starting composition of the anatectic melt and fluid regime during anatexis throughout the upper amphibolite facies, transition, and granulite facies zones. Inclusions have negative crystal shapes, sizes from 2 to 10 μm and are regularly distributed in the core of the garnet. Microstructural and micro‐Raman investigations indicate the presence of two types of inclusions: crystallized silicate melt inclusions (i.e., nanogranitoids, NI), and fluid inclusions (FI). Microstructural evidence suggests that FI and NI coexist in the same cluster and are primary (i.e., were trapped simultaneously during garnet growth). FI have similar compositions in the three zones and comprise variable proportions of CO₂, CH₄, and N₂, commonly with siderite, pyrophyllite, and kaolinite, suggesting a COHN composition of the trapped fluid. The mineral assemblage in the NI contains K‐feldspar, plagioclase, quartz, biotite, muscovite, chlorite, graphite and, rarely, calcite. Polymorphs such as kumdykolite, cristobalite, tridymite, and less commonly kokchetavite, were also found. Rehomogenized NI from the different zones show that all the melts are leucogranitic but have slightly different compositions. In samples from the upper amphibolite facies, melts are less mafic (FeO + MgO = 2.0–3.4 wt%), contain 860–1700 ppm CO₂ and reach the highest H₂O contents (6.5–10 wt%). In the transition zone melts have intermediate H₂O (4.8–8.5 wt%), CO₂ (457–1534 ppm) and maficity (FeO + MgO = 2.3–3.9 wt%). In contrast, melts at granulite facies reach highest CaO, FeO + MgO (3.2–4.7 wt%), and CO₂ (up to 2,400 ppm), with H₂O contents comparable (5.4–8.3 wt%) to the other two zones. Our results represent the first clear evidence for carbonic fluid‐present melting in the Ivrea Zone. Anatexis of metapelites occurred through muscovite and biotite breakdown melting in the presence of a COH fluid, in a situation of fluid–melt immiscibility. The fluid is assumed to have been internally derived, produced initially by devolatilization of hydrous silicates in the graphitic protolith, then as a result of oxidation of carbon by consumption of Fe³⁺‐bearing biotite during melting. Variations in the compositions of the melts are interpreted to result from higher T of melting. The H₂O contents of the melts throughout the three zones are higher than usually assumed for initial H₂O contents of anatectic melts. The CO₂ contents are highest at granulite facies, and show that carbon‐contents of crustal magmas are not negligible at high T. The activity of H₂O of the fluid dissolved in granitic melts decreases with increasing metamorphic grade. Carbonic fluid‐present melting of the deep continental crust represents, together with hydrate‐breakdown melting reactions, an important process in the origin of crustal anatectic granitoids.     

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.     

Lamprophyres of the Tomtor Massif: A result of mixing between potassic and sodic alkaline mafic magmas

The paper presents data on inclusions in minerals of the least modified potassic lamprophyres in a series of strongly carbonatized potassic alkaline ultramafic porphyritic rocks. The rocks consist of diopside, kaersutite, analcime, apatite, and rare phlogopite and titanite phenocrysts and a groundmass, which is made up, along with these minerals, of potassic feldspar and calcite. The diopside and kaersutite phenocrysts display unsystematic multiple zoning. Chemically and mineralogically, the rock is ultramafic foidite and most likely corresponds to monchiquite. Primary and secondary melt inclusions were found in diopside, kaersutite, apatite, and titanite phenocrysts and are classified into three types: sodic silicate inclusions with analcime, potassic silicate inclusions with potassic feldspar, and carbonate inclusions, which are dominated by calcite. Heating and homogenization of the inclusions show that the potassic lamprophyres crystallized from a heterogeneous magma, with consisted of mixing mafic sodic and potassic alkaline magmas enriched in a carbonatite component. The composition of the magmas was close to nepheline and leucite melanephelinite. The minerals crystallized at 1150–1090°C from the sodic melts and at 1200–1250°C from the potassic ones. The sodic mafic melts were richer in Fe than the potassic ones, were the richest in Al, Mn, SO₃, Cl, and H₂O and poorer in Ti and P. The potassic mafic melts were not lamproitic, as follows from the presence of albite in the crystallized primary potassic melt inclusions. The diopside, the first mineral to crystallize in the rock, started to crystallize in the magmatic chamber from sodic mafic melt and ended to crystallize from mixed sodic–potassic melts. The potassic mafic melts were multiply replenished in the chamber in relation to tectonic motions. The ascent of the melts to the surface and rapidly varying P–T parameters of the magma were favorable for multiple separations of carbonatite melts from the alkaline mafic ones and their mixing and mingling.     

Composite carbonate and silicate multiphase solid inclusions in metamorphic garnet from ultrahigh‐P eclogite in the Dabie orogen

Composite multiphase solid (MS) inclusions composed of carbonate and silicate minerals have been found for the first time in metamorphic garnet from ultrahigh‐P eclogite from the Dabie orogen. These inclusions are morphologically euhedral to subhedral, and some show relatively regular shapes approaching the negative crystal shape of the host garnet. Radial fractures often occur in garnet hosting the inclusions. The inclusions are primarily composed of variable proportions of carbonate and silicate minerals such as calcite, quartz, K‐feldspar and plagioclase, with occasional occurrences of magnetite, zircon and barite. They are categorized into two groups based on the proportions of carbonate and silicate phases. Group I is carbonate‐dominated with variable proportions of silicate minerals, whereas Group II is silicate‐dominated with small proportions of carbonates. Trace element analysis by LA‐ICPMS for the two groups of MS inclusions yields remarkable differences. Group I inclusions exhibit remarkably lower REE contents than Group II inclusions, with significant LREE enrichment and large fractionation between LREE and HREE in the chondrite‐normalized REE diagram. In contrast, Group II inclusions show rather flat REE patterns with insignificant fractionation between LREE and HREE. In the primitive mantle‐normalized spidergram, Group I inclusions exhibit positive anomalies of Zr and Hf, whereas Group II inclusions show negative anomalies of Zr and Hf. Nevertheless, both groups exhibit positive anomalies of Ba, U, Pb and Sr, but negative anomalies of Nb and Ta, resembling the composition of common continental crust. Group I inclusions have higher Ba and U contents than Group II inclusions. Combined with petrological observations, the two groups of MS inclusions are interpreted as having crystallized from composite silicate and carbonate melts during continental subduction‐zone metamorphism. The differences in trace element composition between the two groups are primarily attributed to the proportions of carbonate and silicate phases in the MS inclusions. The silicate melts were derived from the breakdown of hydrous minerals such as paragonite and phengite, whereas the occurrence of carbonate melts indicates involvement of carbonate minerals in the partial melting and thus has great bearing on recycling of supracrustal carbon into the mantle. The coexistence of silicate and carbonate melts in the eclogitic garnet provides insights into the nature of hydrous melts in the subduction factory.     

Kankan diamonds (Guinea) I: from the lithosphere down to the transition zone

Peridotitic inclusions in alluvial diamonds from the Kankan region of Guinea in West Africa are mainly of lherzolitic paragenesis. Nevertheless, extreme Cr₂O₃ contents (max. 17 wt%) in some of the exclusively lherzolitic garnets document that the diamond source experienced a previous stage of melt extraction in the spinel stability field. This initial depletion was followed by at least two metasomatic stages: (1) enrichment of LREE and Sr and (2) introduction mainly of MREE–HREE and other HFSE (Ti, Y, Zr, Hf). The Ti- and HFSE-poor character of stage (1) points towards a CHO-rich fluid or carbonatitic melt, the high HFSE in stage (2) favour silicate melts as enriching agent. Eclogitic inclusions are derived from a large depth interval ranging from the lithosphere through the asthenosphere into the transition zone. The occurrence of negative Eu anomalies in garnet and clinopyroxene from both lithosphere and transition zone suggests a possible relationship to subducted oceanic crust. Lithospheric eclogitic inclusions are derived from heterogeneous sources, that may broadly be divided into a low-Ca group with LREE depleted trace element patterns and a high-Ca group representing a source with negative LREE–HREE slope that is moderately enriched in incompatible elements relative to primitive mantle. High-Ca inclusions of majoritic paragenesis are significantly more enriched in incompatible elements, such as in Sr and LREE. Calculated whole rock compositions require metasomatic enrichment even if a derivation from MORB is assumed. Received: 26 January 2000 / Accepted: 18 May 2000