Thermobarometry and fluid evolution of enderbites within the Magondi Mobile Belt, northern Zimbabwe

Metamorphic conditions within arenaceous, calcareous and argillaceous supracrustal rocks of the Magondi Mobile Belt (Zimbabwe) range from greenschist to granulite facies. Within the high-grade segment, basement gneisses of early Proterozoic age and argillaceous rocks of the Mid-Proterozoic Piriwiri Group are intruded by charnockites and enderbites. Metamorphic mineral assemblages and thermobarometric data for enderbitic granulites of Nyaodza show temperatures of 700–800°C and pressures of 5–7 kbar for the peak of granulite-facies metamorphism. Microthermometry and Raman microspectroscopy reveal that CO₂, associated with minor N₂, has been the dominant fluid phase during granulite-facies metamorphism. The chronology of the CO₂ inclusions and the development of microtextures and mineral assemblages in the enderbites indicates that isolated negative crystal shaped CO₂ inclusions in quartz and plagioclase porphyroclasts entrap syn-metamorphic fluids of medium-high densities (0.88–0.90 g/cm³). Lower density (0.71–0.77 g/cm³) CO₂ inclusions in trails and clusters within the same minerals were formed from local re-equilibration and re-entrapment of the former (near-) peak granulitic CO₂ inclusions. As in many other granulites, syn-metamorphic CO₂ is associated with intrusives emplaced near the peak of metamorphism.     

High-density early CO2 fluids in the ultrahigh-temperature granulites of Ihouhaouene (In Ouzzal, Algeria)

Fluid inclusion studies in rocks from the Lower Proterozoic granulites from western Hoggar (Algeria) provide new evidence for the hypothesis that a CO₂-rich, H₂O-poor fluid was present during the high-grade metamorphism. CO₂ inclusions represent the main fluid trapped in the Ihouhaouene ultrahigh-temperature (over 1000 °C) and high-pressure (10 to 14 kbar) granulites. The microthermometric and Raman microspectrometric measurements indicate that the carbonic fluid is mainly composed of CO₂ with minor amounts of CH₄ and N₂ detected in some inclusions (< 4 mol% CH₄). Carbonic fluid densities range from 1.18 to 0.57 g/cm³. The highest densities are recorded in superdense carbonic inclusions presenting evidence of the earliest trapping and they correspond to the fluid densities expected for the P–T conditions of the peak of metamorphism in the area previously determined from mineral geothermobarometers. Lower densities of carbonic fluids mainly result from the reequilibration of earlier trapped fluid inclusions during retrograde metamorphism and final uplift of the metamorphic terrane, but a new influx of carbonic fluids during the retrograde event remains possible. Carbonic fluids can be produced in situ from decarbonation reactions in interlayered impure marbles during the prograde event or derived from CO₂ flushing from underlying basic intrusions. The aqueous fluids present large variations of composition (0.5 to 30 wt.% NaCl equivalent) and densities (1.16 to 0.57 g/cm³). They clearly correspond to post-metamorphic fluids because they mainly occur along microfractures, they do not show any evidence of immiscibility with the carbonic fluids and mixed aquo-carbonic inclusions have not been observed. The percolation of aqueous fluids is related to the Pan-African tectonometamorphic event.     

Reactions and textures in grossular–wollastonite–scapolite calc–silicate granulites from Maligawila, Sri Lanka: evidence for high-temperature isobaric cooling in the meta-sediments of the Highland Complex

Grossular–wollastonite–scapolite calc–silicate granulites from Maligawila in the Buttala klippe, which form part of the overthrusted rocks of the Highland Complex of Sri Lanka, preserve a number of spectacular coronas and replacement textures that could be effectively used to infer their P–T–fluid history. These textures include coronas of garnet, garnet–quartz, and garnet–quartz–calcite at the grain boundaries of wollastonite, scapolite, and calcite as well as calcite–plagioclase and calcite–quartz symplectites or finer grains after scapolite and wollastonite respectively. Other textures include a double rind of coronal scapolite and coronal garnet between matrix garnet and calcite. The reactions that produced these coronas and replacement textures, except those involving clinopyroxene, are modelled in the CaO–Al₂O₃–SiO₂–CO₂ system using the reduced activities. Calculated examples of T–X_CO2 and P–X_CO2 projections indicate that the peak metamorphic temperature of about 900–875 °C at a pressure of 9 kbar and the peak metamorphic fluid composition is constrained to be low in X_CO2 (0.1<X_CO2<0.30). Interpretation of the textural features on the basis of the partial grids revealed that the calc–silicate granulites underwent high-temperature isobaric cooling, from about 900–875 °C to a temperature below 675 °C, following the peak metamorphism. The late-stage cooling was accompanied by an influx of hydrous fluids. The calc–silicate granulites provide evidence for high-temperature isobaric cooling in the meta-sediments of the Highland Complex, earlier considered by some workers to be confined exclusively to the meta-igneous rocks. The coronal scapolite may have formed under open-system metasomatism.     

Stable isotope geochemistry of marbles from the coesite UHP terrains of Dabieshan and Sulu, China

Marbles from Dabieshan and Sulu, China, suffered ultra high pressure (UHP) metamorphism in the coesite–eclogite facies at approximately 700°C and 30 kbars during Triassic continental collision and subduction. The marbles range in isotopic composition from +7 to +25 δ¹⁸O_VSMOW and from 0 to +6 δ¹³C_VPDB. High δ¹³C values are representative of unmodified protoliths and are similar to those of ¹³C-enriched Sinian carbonate rocks from the Yangtze craton. High oxygen isotope ratios reflect pristine protoliths but the low values may have been caused by infiltration of low ¹⁸O meteoric water during diagenesis and dolomitization, by fracture-controlled infiltration of water during subduction, by metamorphic mineral reactions, or by a combination of these processes. No evidence of regional isotopic transport during UHP metamorphism has been found. Sampling on scales of 1 to 100 m shows marbles to be inhomogeneous in both carbon and oxygen isotopes. Only samples separated by less than 10 cm have equilibrated oxygen and carbon isotope compositions. Limited isotopic equilibration between adjacent rocks is consistent with the preservation of unaltered UHP minerals and indicates that the metamorphic fluid–rock system was rock-dominated during and following peak metamorphism. A freely flowing, pervasive fluid phase was not present during UHP metamorphism. There is no evidence of isotopic exchange between marble and the upper mantle into which it was subducted. Correlation of geochemical similarities of UHP marbles with Sinian limestones implies that the subducted edge of the Yangtze craton extends at least as far north as the coesite–eclogite facies rocks of Dabieshan. Deposition of protolith carbonates may have taken place in a cold climate either preceding or following but not coincident with Neoproterozoic glaciation.     

The Influence of Allogenic Water and Sulfuric Acid to Karst Carbon Sink in Karst Subterranean River in Southern Hu’nan

Evaluating the impact of allogenic water and sulfuric acid on karst carbon sink not only helps to improve the accurate calculation of soil CO₂ uptake by rock weathering, but also obtains a complete understanding of the global carbon cycle. Groundwater samples were collected from four karst subterranean rivers watershed within different lithology strata in Wushui Basin, upstream of Beijiang Basin, Hunan Province, for revealing the important impact of silicate weathering on hydrochemistry of groundwater. To estimate the contribution of soil CO₂ uptake by silicate weathering to CO₂ uptake by rock weathering, the Galy model was employed in this article. The important impact of sulfuric acid on CO₂ uptake by carbonate weathering resulting from the substitution of carbonic acid by protons from sulfuric acid was investigated. Our results showed that the concentration of Na⁺, K⁺ and SiO₂ in L01,L02 subterranean river with silicate strata in watershed were higher than that in L03,L04 subterranean river without silicate strata in watershed, which implied that the contribution of silicate weathering to Na⁺,K⁺ and SiO₂ was very important in watershed within silicate strata . The changeable equivalent ratio between (Ca²⁺+Mg²⁺) and HCO₃^- was 1.05 to 1.15, and the value of [Ca²⁺+Mg²⁺]/[HCO₃^-+SO₄^2-] was 0.99 to 1.08. The concentrations of Ca²⁺ and Mg²⁺ exceeded the equivalent concentrations of HC₃^-, and the excess of Ca²⁺ and Mg²⁺cations were compensated by SO₄^2-, which suggested that sulfuric acid has an important influence on carbonate dissolution. The contribution of soil CO₂uptake by silicate weathering to CO₂ consumption in L01 and L02 subterranean river were 3.36% and 2.22%, respectively, whereas the contribution in L03, L04 subterranean river were less than 0.50%, indicating that the contribution of soil CO₂ uptake by silicate weathering was important in the subterranean river basin within silicate strata. Due to the contributions made by sulfuric acid, the CO₂ consumption in four subterranean rivers decreased by 4.84%, 4.52%, 6.20%, 9.36%, respectively.     

First Report of Sapphirine+Quartz Assemblage from Southern India: Implications for Ultrahigh-temperature Metamorphism

We report here for the first time, the occurrence of sapphirine+quartz assemblage in textural equilibrium from quartzo-feldspathic and pelitic granulites from southern India. The sapphirine-bearing rocks occur as layered gneisses associated with pink granite within massive charnockite in Rajapalaiyam area in the southern part of Madurai Block. Sapphirine occurs in three associations: (i) fine-grained subhedral mineral associated with quartz enclosed in garnet, (ii) intergrowth with Al-rich orthopyroxene (up to 9.7 wt.% Al₂O₃), and (iii) in symplectitic intergrowth with orthopyroxene (Al₂O₃= 5.9–6.7 wt.%) and cordierite surrounding garnet. The sapphirine in association with quartz is slightly magnesian (X_Mg = 0.79–0.80) and low in Si content (1.55–1.56 pfu) as compared with those associated with orthopyroxene and cordierite (X_Mg= 0.77–0.79, Si = 1.59–1.63 pfu). The sapphirine+quartz assemblage suggests that the granulites underwent T>1050 °C peak metamorphism. Cores of porphyroblastic orthopyroxene in the sapphirine-bearing rocks shows high-Al₂O₃ content of up to 9.7 wt.%, suggesting T = 1040–1060°C and P = 8 kbar. FMAS reaction of sapphirine+quartz→garnet+sillimanite+cordierite indicates a cooling from sapphirine+quartz stability field after the peak ultrahigh-temperature metamorphism. Slightly lower temperature estimates from ternary feldspar and sapphirine-spinel geothermometers (T = 950–1000°C) also support a post-peak isobaric cooling. Corona textures of orthopyroxene+cordierite (±sapphirine), orthopyroxene+sapphirine, and cordierite+spinel around garnet suggest subsequent decompression. The sapphirine-quartz association and related textures reported in this study have important bearing on the ultrahigh-temperature metamorphism and exhumation history of the Madurai Block as well as on the tectonic evolution of the continental deep crust in southern India.     

A new chemical index of weathering for metamorphic silicate rocks in tropical regions: A study from Sri Lanka

Weathered and fresh samples of metamorphic rocks from Sri Lanka were collected from various localities and analysed for major elements by XRF method (RIGAKU, KG-X System, Japan). The content of water was determined by the ignition method.

The XRF results, obtained from these samples form the basis of a new index of chemical weathering, particularly for Sri Lanka, which is named the Silica-Titania Index, and is calculated as follows: Silica-Titania Index = {(SiO₂/TiO₂)/[(SiO₂/TiO₂) × (Al₂O₃/TiO ₂) × (SiO₂/Al₂O₃)]} × 100(molecular proportions).

The index can be used to determine the degree of weathering in chemically weathered silicate rocks of other countries in tropical regions. A triangular diagram plots the position of this index. The point load strengths of fresh rocksand weathered rocks with different degrees of weathering were correlated with the values of this new chemical index. The relative variation in strengths of fresh rocks and weathered rocks clearly indicates its suitability and usefulness for engineering geologists.     

Persistence of pre-metamorphic C and O isotopic signatures in marbles subject to Pan-African granulite-facies metamorphism and U–Th mineralization (Tranomaro, Southeast Madagascar)

The status of fluid regimes during the Pan-African granulite-facies metamorphism in Southern Madagascar was examined by means of a mineralogical and stable isotope study of marble lithologies. In the granulitic Tranomaro area, which is made up of metasedimentary rocks (metapelitic, leptynitic (felsic) and calc–silicate metasediments) and intruded by syn-granulitic granitic bodies, syn-granulitic mineralization (Th–U) and metasomatic transformations (marbles→pyroxenites) demonstrate that fluid circulation has occurred. The Tranomaro marbles can be subdivided into two compositional groups, either Mg-poor or Mg-rich. This division reflects pre-metamorphic compositional differences rather than different histories. On a regional scale, the marbles display a large variation in (from +19 to +6.5‰ relative to SMOW) but have a more restricted range (from +1.4 to −2.5‰ relative to PDB). The lowest values are observed in magnesian marbles, whereas calcic ones do not have values lower than +13.5‰. Both initially low and high marbles may have locally been infiltrated by the syn-metamorphic fluid flow which gave rise to pyroxenites and Th–U ores (thorianite). values of carbonate in Mg-rich marbles evolve from +7 up to 8.5‰ towards the contact with a metasomatic pyroxenite in a meter-scale profile across an infiltration zone. The mineralogy, as well as the large and small-scale isotopic results argue for: (i) a pre-metamorphic origin for the isotopic variations, probably related to pre-granulitic dolomitization, (ii) a lack of pervasive fluid infiltration capable of erasing pre-metamorphic isotopic compositional differences, (iii) an absence of mantle-derived C-bearing fluids in the infiltrated zones. For the area as a whole, the present data are consistent with the decarbonation of impure siliceous limestones and dolostones coupled with fluid release from syn-metamorphic granitic intrusions.     

Carbonatite melt–CO2 fluid inclusions in mantle xenoliths from Tenerife, Canary Islands: a story of trapping, immiscibility and fluid–rock interaction in the upper mantle

Three types of fluid inclusions have been identified in olivine porphyroclasts in the spinel harzburgite and lherzolite xenoliths from Tenerife: pure CO₂ (Type A); carbonate-rich CO₂–SO₂ mixtures (Type B); and polyphase inclusions dominated by silicate glass±fluid±sp±silicate±sulfide±carbonate (Type C). Type A inclusions commonly exhibit a “coating” (a few microns thick) consisting of an aggregate of a platy, hydrous Mg–Fe–Si phase, most likely talc, together with very small amounts of halite, dolomite and other phases. Larger crystals (e.g. (Na,K)Cl, dolomite, spinel, sulfide and phlogopite) may be found on either side of the “coating”, towards the wall of the host mineral or towards the inclusion center. These different fluids were formed through the immiscible separations and fluid–wall-rock reactions from a common, volatile-rich, siliceous, alkaline carbonatite melt infiltrating the upper mantle beneath the Tenerife. First, the original siliceous carbonatite melt is separated from a mixed CO₂–H₂O–NaCl fluid and a silicate/silicocarbonatite melt (preserved in Type A inclusions). The reaction of the carbonaceous silicate melt with the wall-rock minerals gave rise to large poikilitic orthopyroxene and clinopyroxene grains, and smaller neoblasts. During the metasomatic processes, the consumption of the silicate part of the melt produced carbonate-enriched Type B CO₂–SO₂ fluids which were trapped in exsolved orthopyroxene porphyroclasts. At the later stages, the interstitial silicate/silicocarbonatite fluids were trapped as Type C inclusions. At a temperature above 650 °C, the mixed CO₂–H₂O–NaCl fluid inside the Type A inclusions were separated into CO₂-rich fluid and H₂O–NaCl brine. At T<650 °C, the residual silicate melt reacted with the host olivine, forming a reaction rim or “coating” along the inclusion walls consisting of talc (or possibly serpentine) together with minute crystals of NaCl, KCl, carbonates and sulfides, leaving a residual CO₂ fluid. The homogenization temperatures of +2 to +25 °C obtained from the Type A CO₂ inclusions reflect the densities of the residual CO₂ after its reactions with the olivine host, and are unrelated to the initial fluid density or the external pressure at the time of trapping. The latter are restricted by the estimated crystallization temperatures of 1000–1200 °C, and the spinel lherzolite phase assemblage of the xenolith, which is 0.7–1.7 GPa.     

Oxygen, carbon, and strontium isotope geochemistry of diamond-bearing carbonate rocks from Kumdy-Kol, Kokchetav Massif, Kazakhstan

Diamond-bearing carbonate rocks from Kumdy-Kol, Kokchetav massif, Kazakhstan, were strongly altered by fluids flowing through fractures and infiltrating along grain boundaries during exhumation. Alteration includes retrogradation of high-grade silicate assemblages by hydrous minerals, replacement of diamond by graphite and of dolomite by calcite. Diamond-bearing carbonate rocks are among the most intensely altered isotopically with δ¹⁸O_VSMOW values as low as +9‰, δ¹³C_VPDB=−9‰, and ⁸⁷Sr/⁸⁶Sr as high as 0.8050. Evidence of isotopic equilibration between coexisting dolomite and high-Mg calcite during ultrahigh-pressure metamorphism (UHPM) is preserved only rarely in samples isolated from infiltrating fluids by distance from fractures. Isotopic heterogeneity and isotopic disequilibrium are widespread on a hand-specimen scale. Because of this lack of homogeneity, bulk analyses cannot provide definitive measurements of ¹³C/¹²C fractionation between coexisting diamond and carbonate. Our study adequately documents alteration on a scale commensurate with observed vein structures. But, testing the hypothesis of metamorphic origin of microdiamonds has not fully succeeded because our analytical spatial resolution, limited to 0.5 mm, is not small enough to measure individual dolomite inclusions or individual diamond crystals.     

Torngat ultramafic lamprophyres and their relation to the North Atlantic Alkaline Province

Geological mapping and diamond exploration in northern Quebec and Labrador has revealed an undeformed ultramafic dyke swarm in the northern Torngat Mountains. The dyke rocks are dominated by an olivine-phlogopite mineralogy and contain varying amounts of primary carbonate. Their mineralogy, mineral compositional trends and the presence of typomorphic minerals (e.g. kimzeyitic garnet), indicate that these dykes comprise an ultramafic lamprophyre suite grading into carbonatite. Recognized rock varieties are aillikite, mela-aillikite and subordinate carbonatite. Carbonatite and aillikite have in common high carbonate content and a lack of clinopyroxene. In contrast, mela-aillikites are richer in mafic silicate minerals, in particular clinopyroxene and amphibole, and contain only small amounts of primary carbonate. The modal mineralogy and textures of the dyke varieties are gradational, indicating that they represent end-members in a compositional continuum.

The Torngat ultramafic lamprophyres are characterized by high but variable MgO (10–25 wt.%), CaO (5–20 wt.%), TiO₂ (3–10 wt.%) and K₂O (1–4 wt.%), but low SiO₂ (22–37 wt.%) and Al₂O₃ (2–6 wt.%). Higher SiO₂, Al₂O₃, Na₂O and lower CO₂ content distinguish the mela-aillikites from the aillikites. Whereas the bulk rock major and trace element concentrations of the aillikites and mela-aillikites overlap, there is no fractional crystallization relation between them. The major and trace element characteristics imply related parental magmas, with minor olivine and Cr-spinel fractionation accounting for intra-group variation.

The Torngat ultramafic lamprophyres have a Neoproterozoic age and are spatially and compositionally closely related with the Neoproterozoic ultramafic lamprophyres from central West Greenland. Ultramafic potassic-to-carbonatitic magmatism occurred in both eastern Laurentia and western Baltica during the Late Neoproterozoic. It can be inferred from the emplacement ages of the alkaline complexes and timing of Late Proterozoic processes in the North Atlantic region that this volatile-rich, deep-seated igneous activity was a distal effect of the breakup of Rodinia. This occurred during and/or after the rift-to-drift transition that led to the opening of the Iapetus Ocean.     

Magma–host interactions during differentiation and emplacement of a shallow-level, zoned granitic pluton (Tarçouate pluton, Morocco): implications for magma emplacement

The Tarçouate pluton (Anti-Atlas, Morocco) is an inversely zoned laccolith emplaced 583 Ma ago into low-grade metasediments, with the following succession: leucocratic granites, biotite–granodiorites (±monzodiorites), hornblende–granodiorites (±monzodiorites) and monzodiorites syn-plutonic dykes. These rocks form two distinct, chemically coherent, units:

(1) A main unit consists of layered (572<59 wt.%) and homogeneous (632<67%) hornblende–granodiorites, biotite–granodiorites (672<72%) and aplites (702<76%). All these rocks are metaluminous to peraluminous and display fractionated HREE depleted patterns (La/Yb_N=14–61; Yb_N=0.7–6.8). Initial ⁸⁷Sr/⁸⁶Sr ratios (0.7072 to 0.7080) increase, whereas _Nd(t) values (−1.7 to −2.8) decrease from the hornblende– to the biotite–granodiorites. Monzodiorites occur as mafic microgranular enclaves or syn-plutonic dykes.

(2) A subordinate unit consists of leucocratic, distinctly peraluminous, muscovite-bearing granites (722<75%) occurring at the northern edge of the pluton and as dykes in the surrounding schists towards the top of the pluton. These rocks are free of monzodioritic enclaves. They display less fractionated patterns with higher HREE contents (La/Yb_N=2–19; Yb_N=11–18), a distinct _Nd(t) value (−11.8) and a ⁸⁷Sr/⁸⁶Sr initial ratio (0.7480) within those of the surrounding schists (0.7393–0.7819).

Magma–host interactions are closely related to differentiation and occurred at different levels, but mainly before emplacement. Field relationships and petrogenetic modelling show that the bt–granodiorites formed at levels deeper than the level of emplacement, by fractional crystallisation (0.65

These data preclude any significant material transfer process for the emplacement of the Tarçouate pluton, but rather suggest assembly of successive pulses of variably differentiated crystal-poor magmas. These shallow level granitic plutons can be considered as an end-member of magma emplacement with minimum interactions with the country rocks.     

Petrology, Origin and Metamorphic History of Proterozoic-aged Granulites of the Natal Metamorphic Province, Southeastern Africa

The geochemistry of the Leisure Bay Formation, Natal Metamorphic Province suggests that its protoliths were greywackes, pelites and arkoses that were deposited in an oceanic island arc environment. These rocks contain the mineral assemblage biotite + hypersthene + cordierite (with hercynite inclusions) + garnet + quartz + feldspar. Numerous generations of garnet genesis are evident from which a long history of metamorphism can be interpreted. M₁ involved syn-D₁ high temperature/low pressure metamorphism (4kb and >850^oC) and dehydration melting to produce essentially anhydrous assemblages particularly in the vicinity of, and probably related to the intrusion of the Munster Suite sills. The inclusions of hercynite in cordierite and the garnet + quartz symplectites after hypersthene + plagioclase (550^oC and 5kb) suggests isobaric cooling after M₁. This indicates an anticlockwise P-T loop related to the early intrusion of subduction related calc-alkaline magmatic rocks. M₂ involved syn-D₂ dehydration melting of hydrous assemblages possibly related to the emplacement of many A-type rapakivi charnockite granitoids, which provided heat and loading. The D₂ tectonism post-dated all lithologies in the region, except for syn- to late-D₂ granitoid plutons, and is interpreted as a transpressional tectonothermal reworking of pre-existing (Proterozoic) crust at 1030Ma.     

Fluid inclusions in Scourian granulites from the Lewisian complex of NW Scotland: evidence for CO2-rich fluid in Late Archaean high-grade metamorphism

In this paper the first fluid-inclusion data are presented from Late Archaean Scourian granulites of the Lewisian complex of mainland northwest Scotland. Pure CO₂ or CO₂-dominated fluid inclusions are moderately abundant in pristine granulites. These inclusions show homogenization temperatures ranging from − 54 to + 10 °C with a very prominent histogram peak at − 16 to − 32 °C. Isochores corresponding to this main histogram peak agree with P-T estimates for granulite-facies recrystallization during the Badcallian (750–800 °C, 7–8 kbar) as well as with Inverian P-T conditions (550–600 °C, 5 kbar). The maximum densities encountered could correspond to fluids trapped during an early, higher P-T phase of the Badcallian metamorphism (900–1000 °C, 11–12 kbar). Homogenization temperatures substantially higher than the main histogram peak may represent Laxfordian reworking (≤ 500 °C, < 4 kbar). In the pristine granulites, aqueous fluid inclusions are of very subordinate importance and occur only along late secondary healed fractures. In rocks which have been retrograded to amphibolite facies from Inverian and/or Laxfordian shear zones, CO₂ inclusions are conspicuously absent; only secondary aqueous inclusions are present, presumably related to post-granulite hydration processes. These data illustrate the importance of CO₂-rich fluids for the petrogenesis of Late Archaean granulites, and demonstrate that early fluid inclusions may survive subsequent metamorphic processes as long as no new fluid is introduced into the system.     

等压扩散下CO2对不同变质程度煤中CH4置换效应的影响

为了研究等压扩散条件下不同变质程度煤中CO₂置换CH₄特征规律,选择无烟煤、瘦煤和气肥煤3种煤样,进行了不同等压扩散压力下的等压扩散置换实验。实验结果表明:随着煤变质程度的增加煤吸附CH₄和CO₂的能力表现出逐渐增强的趋势,且CO₂的吸附量大于CH₄的吸附量;随着实验点扩散压力的增加,CO₂对CH₄的绝对置换量和置换率均随之增加,CO₂对CH₄的注置比却随之降低。在实验煤样变质程度范围内,CH₄置换率与煤变质程度和CO₂注置比均呈负相关关系。研究成果对井下注CO₂置换煤层CH₄的工程技术和理论具有指导意义。      

Comparison of petrogenetic signatures between mantle-derived alkali silicate intrusives with and without associated carbonatite, Namibia

We compare the petrogenetic and chemical signatures of two alkali silicate suites from the Cretaceous Damaraland igneous province (Namibia), one with and one without associated carbonatite, in order to explore their differences in terms of magma source and evolution. The Etaneno complex occurs in close spatial proximity to the Kalkfeld bimodal carbonatite–alkali silicate complex, and is dominated by nepheline (ne)-monzosyenites and ne-bearing alkali feldspar syenites. The Etaneno samples have isotopic compositions of ⁸⁷Sr/⁸⁶Sr(i)=0.70462–0.70508 and Nd=−0.5 to −1.5, with the highest ⁸⁷Sr/⁸⁶Sr(i) and lowest Nd values observed in evolved samples. The magma differentiated via olivine, feldspar, clinopyroxene, and nepheline (ne) fractionation in a F-rich system, which fractionated Zr from Hf, and Y from Ho. Partly glassy, recrystallized inclusions in some samples are less evolved than their host rocks and contain a cumulate component (nepheline, plagioclase). The Kalkfeld ne-foidites (ijolites) and ne-syenites have ⁸⁷Sr/⁸⁶Sr(i)=0.70285–0.70592 and Nd=0.5 to 1.1. The isotope ratios show no consistent variation with rock composition, and they are in the same range as the associated carbonatites. The Kalkfeld silicate magma fractionated nepheline and alkali-feldspar in a CO₂-dominated, F- and Ca-poor system. As a result, the rocks display some major and trace element trends distinctly different from those of the Etaneno samples.

We suggest that the Etaneno and the Kalkfeld magmas represent different melt fractions of a heterogeneous mantle source, resulting in different compositions especially with respect to CO₂ contents of the primitive, parental magmas. In this scenario, the carbonated alkali silicate Kalkfeld parental melt contained a critical CO₂ concentration and underwent liquid separation of carbonate and silicate melt fractions at crustal depths. The resulting silicate melt fraction experienced a very different mode of differentiation than the carbonate-poor Etaneno parental magma. Thus, the Kalkfeld rocks are depleted in Ca and other divalent cations, as well as F, rare-earth elements (REE), Ba, and P relative to the Etaneno syenites. We interpret these differences to reflect the partitioning of these elements into the carbonate melt fraction during immiscible separation.     

Two-stage corona growth during Precambrian granulite facies metamorphism of Smitbson Bjerge, north-west Greenland

Abstract Late Archaean orthogneisses and aluminous and iron-rich metasedimentary rocks intruded by anorthosite and a ferrodiorite-granite suite were completely recrystallized during Proterozoic granulite facies metamorphism. Geobarometry and geothermometry indicate P-T conditions of around 7.5kbar. 700°C, with a CO₂-rich fluid phase and logfO₂ at or below -16. A two-stage high-grade history of near isochemical corona growth is preserved in metasediments with the reaction cycle opx + plag + H₂O → hbl+gar+SiO₂→ opx+plag+H₂O. End product compositions resemble those of the initial phases, and the only mobile components were SiO₂ and/or H₂O. The coronas reflect shortlived fluctuations in chemical activity at essentially constant P and T, contrary to simple progressive change in equilibrium parameters recorded by most corona-bearing textures.     

Two types of gneisses associated with eclogite at Shuanghe in the Dabie terrane: carbon isotope, zircon U–Pb dating and oxygen isotope

There are two types of gneisses, biotite paragneiss and granitic orthogneiss, to be closely associated with UHP eclogite at Shuanghe in the Dabie terrane. Both concentration and isotope composition of bulk carbon in apatite and host gneisses were determined by the EA-MS online technique. Structural carbonate within the apatite was detected by the XRD and FTIR techniques. Significant ¹³C-depletion was observed in the apatite with δ¹³C values of −28.6‰ to −22.3‰ and the carbon concentrations of 0.70–4.98 wt.% CO₂ despite a large variation in δ¹⁸O from −4.3‰ to +10.6‰ for these gneisses. There is significant heterogeneity in both δ¹³C and δ¹⁸O within the gneisses on the scale of several tens meters, pointing to the presence of secondary processes after the UHP metamorphism. Considerable amounts of carbonate carbon occur in some of the gneisses that were also depleted in ¹³C primarily, but subjected to overprint of ¹³C-rich CO₂-bearing fluid after the UHP metamorphism. The ¹³C-depleted carbon in the gneisses is interpreted to be inherited from their precursors that suffered meteoric–hydrothermal alteration before plate subduction. Both low δ¹³C values and structural carbonate in the apatite suggest the presence of ¹³C-poor CO₂ in the UHP metamorphic fluid. The ¹³C-poor CO₂ is undoubtedly derived from oxidation of organic matter in the subsurface fluid during the prograde UHP metamorphism.

Zircons from two samples of the granitic orthogneiss exhibit low δ¹⁸O values of −4.1‰ to −1.1‰, demonstrating that its protolith was significantly depleted in ¹⁸O prior to magma crystallization. U–Pb discordia datings for the ¹⁸O-depleted zircons yield Neoproterozoic ages of 724–768 Ma for the protolith of the granitic orthogneiss, consistent with protolith ages of most eclogites and orthogneisses from the other regions in the Dabie–Sulu orogen. Therefore, the meteoric–hydrothermal alteration is directly dated to occur at mid-Neoproterozoic, and may be correlated with the Rodinia supercontinental breakup and the snowball Earth event. It is thus deduced that the igneous protolith of the granitic orthogneiss and some eclogites would intrude into the older sequences composing the sedimentary protoliths of the biotite paragneiss and some eclogites along the northern margin of the Yangtze plate at mid-Neoproterozoic, and drove local meteoric–hydrothermal circulation systems in which both ¹³C- and ¹⁸O-depleted fluid interacted with the protoliths of these UHP rocks now exposed in the Dabie terrane.     

Geochronology and petrogenesis of Pan-African, syn-tectonic, S-type and post-tectonic A-type granite (Namibia): products of melting of crustal sources, fractional crystallization and wall rock entrainment

The Oetmoed Granite–Migmatite Complex (OGMC), Central Damara Orogen, Namibia, consists mainly of 526 to 516 Ma garnet- and cordierite-bearing granite and subordinate 488 to 494 Ma hornblende- and titanite-bearing granite in the form of planar sheets and dykes. Additionally, a slightly elongated granite body occurs in the center of the complex. The garnet- and cordierite-bearing granite has major- and trace-element characteristics of S-type granite but the hornblende- and titanite-bearing granite has higher HFSE and REE contents similar to A-type granite. Whereas the garnet- and cordierite-bearing granite contains numerous restitic xenoliths, the hornblende- and titanite-bearing granite is xenolith-free. The country rocks are cordierite–sillimanite–K-feldspar–garnet-bearing metasedimentary rocks and migmatite. Cordierite- and garnet-rich xenoliths in the S-type granite do not represent primary restite, their depleted chemical composition is best explained by varying and large degrees of partial melting of incorporated country rocks. Most chemical variations among the garnet- and cordierite-bearing granite can be explained by processes linked with fractional crystallization of plagioclase, biotite and accessory phases, mostly monazite and zircon. Major and trace element data and high δ ¹⁸O values suggest that the least evolved members of the garnet- and cordierite-bearing granite were derived from metapelitic rocks at ca. 800°C as inferred from monazite and apatite dissolution thermometry. Higher CaO and Na₂O but lower SiO₂ contents and lower Rb/Sr ratios as well as lower δ ¹⁸O values of the hornblende- and titanite-bearing granite suggest that they are more likely generated by partial melting of non-pelitic sources (metagranitoids?) at temperatures in excess of 900°C. Decreasing TiO₂, Na₂O, FeO_tot., MgO, CaO, total REE content but increasing Al₂O₃ and K₂O indicate fractionation of mainly hornblende and titanite in the case of the hornblende- and titanite-bearing granite. The differing compositions of the garnet- and cordierite-bearing granite and the hornblende- and titanite-bearing granite are attributed to different source rocks (metapelite instead of metagranitoid) and different temperatures during melting as inferred from accessory phase dissolution thermometry. Furthermore, significant entrainment of country rock in some samples played a major role during petrogenesis of the garnet- and cordierite-bearing granite but was not important during the evolution of the hornblende- and titanite-bearing granite. Intrusion of such hot, felsic magmas close to the inferred peak of metamorphism has probably caused, in part, the high temperature metamorphism and anatexis of the country rocks at relatively low pressures.     

Le facies granulite en Norvege Meridionale II. Les inclusions fluides

Liquid inclusions in quartz found in rocks of amphibolite and of granulite facies were studied. In the former water is predominant, in the latter CO₂ (probably juvenile). Estimates of PT conditions during metamorphism based on the study of inclusions gave values (800°C, 8 kb) comparable to those obtained by the petrological study (7–800 °C, 6–8 kb) presented in part I.