1.8 Ga Svecofennian post-collisional shoshonitic magmatism in the Fennoscandian shield

At least 14 small (1–11 km across) 1.8 Ga Svecofennian post-collisional bimodal intrusions occur in southern Finland and Russian Karelia in a 600-km-long belt from the Åland Islands to the NW Lake Ladoga region. The rocks range from ultramafic, calc-alkaline, apatite-rich potassium lamprophyres to peraluminous HiBaSr granites, and form a shoshonitic series with K₂O+Na₂O>5%, K₂O/Na₂O>0.5, Al₂O₃>9% over a wide spectrum of SiO₂ (32–78%). Although strongly enriched in all rocks, the LILE Ba and Sr and the LREE generally define a decreasing trend with increasing SiO₂. Depletion is noted for HFSE Ti, Nb and Ta. Available isotopic data show overlapping values for lamprophyres and granites within separate intrusions and a cogenetic origin is thus not precluded. Initial magmas (Mg#>65) in this shoshonitic association are considered to be generated in an enriched lithospheric mantle during post-collisional uplift some 30 Ma after the regional Svecofennian metamorphic peak. However, prior to the melting episode, the lithospheric mantle was affected by carbonatite metasomatism; more extensively in the east than in the west. The melts generated in the more carbonate-rich mantle are extremely enriched in P₂O₅4%, F12,000 ppm, LILE: Ba9000 ppm, Sr7000 ppm, LREE: La600 ppm and Ce1000 ppm. The parental magma underwent 55–60% fractionation of biotite+clinopyroxene+apatite+magnetite+sphene whereupon intermediate varieties were produced. After further fractionation, 60–80%, of K-feldspar+amphibole+plagioclase±(minor magnetite, sphene and apatite), leucosyenites and quartz-monzonites were formed. In the west, where the source was less affected by carbonatite metasomatism, calc-alkaline lamprophyres (vogesites, minettes and spessartites) and equivalent plutonic rocks (monzonites) were formed. Removal of about 50% of biotite, amphibole, plagioclase, magnetite, apatite and sphene produced peraluminous HiBaSr granites. The impact of crustal assimilation is considered to be low. At about 1.8 Ga, the post-collisional shoshonitic magmatism brought juvenile material, particularly enriched in alkalis, LILE, LREE and F, into the crust. Although areally restricted, the regional distribution of the post-collisional intrusions may indicate that larger volumes of 1.8 Ga juvenile material resides in unexposed parts of the crust.     

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.     

Petrogenesis of A-type granites and origin of vertical zoning in the Katharina pluton, Gebel Mussa (Mt. Moses) area, Sinai, Egypt

The central pluton within the Neoproterozoic Katharina Ring Complex (area of Gebel Mussa, traditionally believed to be the biblical Mt. Sinai) shows a vertical compositional zoning: syenogranite makes up the bulk of the pluton and grades upwards to alkali-feldspar granites. The latters form two horizontal subzones, an albite–alkali feldspar (Ab–Afs) granite and an uppermost perthite granite. These two varieties are chemically indistinguishable. Syenogranite, as compared with alkali-feldspar granites, is richer in Ca, Sr, K, Ba and contains less SiO₂, Rb, Y, Nb and U; Eu/Eu* values are 0.22–0.33 for syenogranite and 0.08–0.02 for alkali-feldspar granites. The δ¹⁸O (Qtz) is rather homogeneous throughout the pluton, 8.03–8.55‰. The δ¹⁸O (Afs) values in the syenogranite are appreciably lower relative to those in the alkali–feldspar granites: 7.59–8.75‰ vs. 8.31–9.12‰. A Rb–Sr isochron (n = 9) yields an age of 593 ± 16 Ma for the Katharina Ring Complex (granite pluton and ring dikes).

The alkali–feldspar granites were generated mainly by fractional crystallization of syenogranite magma. The model for residual melt extraction and accumulation is based on the estimated extent of crystallization ( 50 wt.%), which approximates the rigid percolation threshold for silicic melts. The fluid-rich residual melt could be separated efficiently by its upward flow through the rigid clusters of crystal phase. Crystallization of the evolved melt started with formation of hypersolvus granite immediately under the roof. Fluid influx from the inner part of the pluton to its apical zone persisted and caused increase of P_H2O in the magma below the perthite granite zone. Owing to the presence of F and Ca in the melt, P_H2O of only slightly more than 1 kbar allows crystallization of subsolvus Ab–Afs granite. Abundance of turbid alkali feldspars and their ¹⁸O/¹⁶O enrichment suggest that crystallization of alkali-feldspar granites was followed by subsolvus fluid–rock interaction; the δ¹⁸O (Fsp) values point to magmatic origin of fluids.

The stable and radiogenic isotope data [δ¹⁸O (Zrn) = 5.82 ± 0.06‰, I_Sr = 0.7022 ± 0.0064, ε_Nd (T) values are + 3.6 and + 3.9] indicate that the granite magma was generated from a ‘juvenile’ source, which is typical of the rocks making up most of the Arabian–Nubian shield.     

Geochemical and Sr–Nd–Pb isotopic compositions of the Eocene Dölek and Sariçiçek Plutons, Eastern Turkey: Implications for magma interaction in the genesis of high-K calc-alkaline granitoids in a post-collision extensional setting

The major and trace elements and Sr–Nd–Pb isotopes of the host rocks and the mafic microgranular enclaves (MME) gathered from the Dölek and Sariçiçek plutons, Eastern Turkey, were studied to understand the underlying petrogenesis and geodynamic setting. The plutons were emplaced at  43 Ma at shallow depths ( 5 to 9 km) as estimated from Al-in hornblende geobarometry. The host rocks consist of a variety of rock types ranging from diorite to granite (SiO₂ = 56.98–72.67 wt.%; Mg# = 36.8–50.0) populated by MMEs of gabbroic diorite to monzodiorite in composition (SiO₂ = 53.21–60.94 wt.%; Mg# = 44.4–53.5). All the rocks show a high-K calc-alkaline differentiation trend. Chondrite-normalized REE patterns are moderately fractionated and relatively flat [(La/Yb)_N = 5.11 to 8.51]. They display small negative Eu anomalies (Eu/Eu = 0.62 to 0.88), with enrichment of LILE and depletion of HFSE. Initial Nd–Sr isotopic compositions for the host rocks are ε_Nd(43 Ma) = − 0.6 to 0.8 and mostly I_Sr = 0.70482–0.70548. The Nd model ages (T_DM) vary from 0.84 to 0.99 Ga. The Pb isotopic ratios are (²⁰⁶Pb/²⁰⁴Pb) = 18.60–18.65, (²⁰⁷Pb/²⁰⁴Pb) = 15.61–15.66 and (²⁰⁸Pb/²⁰⁴Pb) = 38.69–38.85. Compared with the host rocks, the MMEs are relatively homogeneous in isotopic composition, with I_Sr ranging from 0.70485 to 0.70517, ε_Nd(43 Ma) − 0.1 to 0.8 and with Pb isotopic ratios of (²⁰⁶Pb/²⁰⁴Pb) = 18.58–18.64, (²⁰⁷Pb/²⁰⁴Pb) = 15.60–15.66 and (²⁰⁸Pb/²⁰⁴Pb) = 38.64–38.77. The MMEs have T_DM ranging from 0.86 to 1.36 Ga. The geochemical and isotopic similarities between the MMEs and their host rocks indicate that the enclaves are of mixed origin and are most probably formed by the interaction between the lower crust- and mantle-derived magmas. All the geochemical data, in conjunction with the geodynamic evidence, suggest that a basic magma derived from an enriched subcontinental lithospheric mantle, probably triggered by the upwelling of the asthenophere, and interacted with a crustal melt that originated from the dehydration melting of the mafic lower crust at deep crustal levels. Modeling based on the Sr–Nd isotope data indicates that  77–83% of the subcontinental lithospheric mantle involved in the genesis. Consequently, the interaction process played an important role in the genesis of the hybrid granitoid bodies, which subsequently underwent a fractional crystallization process along with minor amounts of crustal assimilation, en route to the upper crustal levels generating a wide variety of rock types ranging from diorite to granite in an extensional regime.     

Status report on stability of K-rich phases at mantle conditions

Experimental research on K-rich phases and observations from diamond inclusions, UHP metamorphic rocks, and xenoliths provide insights about the hosts for potassium at mantle conditions. K-rich clinopyroxene (Kcpx–KM³⁺Si₂O₆) can be an important component in clinopyroxenes at P>4 GPa, dependent upon coexisting K-bearing phases (solid or liquid) but not, apparently, upon temperature. Maximum Kcpx content can reach 25 mol%, with 17 mol% the highest reported in nature. Partitioning ^(K)D_(cpx/liquid) above 7 GPa=0.1–0.2 require ultrapotassic liquids to form highly potassic cpx or critical solid reactions, e.g., between Kspar and Di. Phlogopite can be stable to about 8 GPa at 1250 °C where either amphibole or liquid forms. When fluorine is present, it generally increases in Phl upon increasing P (and probably T) to about 6 GPa, but reactions forming amphibole and/or KMgF₃ limit F content between 6 and 8 GPa. The perovskite KMgF₃ is stable up to 10 GPa and 1400 °C as subsolidus breakdown products of phlogopite upon increasing P. ^(M4)K-substituted potassic richterite (ideally K(KCa)Mg₅Si₈O₂₂(OH,F)₂) is produced in K-rich peridotites above 6 GPa and in Di+Phl from 6 to 13 GPa. K content of amphibole is positively correlated with P; Al and F content decrease with P. In the system 1Kspar+1H₂O K-cymrite (hydrous hexasanidine–KAlSi₃O₈·nH₂O–Kcym) is stable from 2.5 GPa at 400 to 1200 °C and 9 GPa; Kcym can be a supersolidus phase. Formation of Kcym is sensitive to water content, not forming within experiments with H₂O2O>Kspar. Phase X, a potassium di-magnesium acid disilicate ((K_1−x−n)₂(Mg_1−nM_n³⁺)₂Si₂O₇H_2x), forms in mafic compositions at T=1150–1400 °C and P=9–17 GPa and is a potential host for K and H₂O at mantle conditions with a low-T geotherm or in subducting slabs. The composition of phase-X is not fixed but actually represents a solid solution in the stoichiometries □₂Mg₂Si₂O₇H₂–(K□)Mg₂Si₂O₇H–K₂Mg₂Si₂O₇ (□=vacancy), apparently stable only near the central composition. K-hollandite, KAlSi₃O₈, is possibly the most important K-rich phase at very high pressure, as it appears to be stable to conditions near the core–mantle boundary, 95 GPa and 2300 °C. Other K-rich phases are considered.     

Origin and evolution of Pliocene–Pleistocene granites from the Larderello geothermal field (Tuscan Magmatic Province, Italy)

Extensive, mainly acidic peraluminous magmatism affected the Tuscan Archipelago and the Tuscan mainland since late Miocene, building up the Tuscan Magmatic Province (TMP) as the Northern Apennine fold belt was progressively thinned, heated and intruded by mafic magmas. Between 3.8 and 1.3 Ma an intrusive complex was built on Larderello area (Tuscan mainland) by emplacement of multiple intrusions of isotopically and geochemically distinct granite magmas. Geochemical and isotopic investigations were carried out on granites cored during drilling exploration activity on the Larderello geothermal field. With respect to the other TMP granites the Larderello intrusives can be classified as two-mica granites due to the ubiquitous presence of small to moderate amounts of F-rich magmatic muscovite. They closely resemble the almost pure crustal TMP acidic rocks and do not show any of the typical petrographic features commonly observed in the TMP hybrid granites (enclaves, patchy zoning of plagioclase, amphibole clots). On the basis of major and trace elements, as well as REE patterns, two groups of granites were proposed: LAR-1 granites (3.8–2.3 Ma) originated by biotite-muscovite breakdown, and LAR-2 granites (2.3–1.3 Ma) generated by muscovite breakdown. At least three main crustal sources (at 14–23 km depth), characterized by distinct ε_Nd(t) and ⁸⁷Sr/⁸⁶Sr values, were involved at different times, and the magmas produced were randomly emplaced at shallow levels (3–6 km depth) throughout the entire field. The partial melting of a biotite-muscovite-rich source with low ε_Nd(t) value (about −10.5) produced the oldest intrusions (about 3.8–2.5 Ma). Afterwards (2.5–2.3 Ma), new magmas were generated by another biotite-rich source having a distinctly higher ε_Nd(t) value (−7.9). Finally, a muscovite-rich source with high ε_Nd(t) (about −8.9) gave origin to the younger group of granites (2.3–1.0 Ma). The significant Sr isotope disequilibrium recorded by granites belonging to the same intrusion is interpreted, as due to the short residence time of magmas in the source region followed by their rapid transfer to the emplacement level. Partial melting was probably triggered by multiple, small-sized mafic intrusions, distributed over the last 3.8 Ma that allowed temporary overstepping of biotite- and muscovite-dehydration melting reactions into an already pre-heated crust. Dilution in time of the magmatic activity probably prevented melt mingling and homogenization at depth, as well as the formation of a single, homogeneous, hybrid pluton at the emplacement level. Moreover the high concentrations of fluxing elements (B, F, Li) estimated for the LAR granites modified melt properties by reducing solidus temperatures, decreasing viscosity and increasing H₂O solubility in granite melts. The consequences were a more efficient, fast, magma extraction and transfer from the source, and a prolonged time of crystallization at the emplacement level. These key factors explain the long-lived hydrothermal activity recorded in this area by both fossil (Plio-Quaternary ore deposits) and active (Larderello geothermal field) systems.     

赣西北小九宫-沙店白垩纪花岗岩的岩石成因及构造意义

赣西北-湘东北地区出露较多晚中生代花岗岩,并与中、下扬子地区晚中生代花岗岩组成一条NEE向岩浆岩带.通过对赣西北小九宫和沙店花岗岩进行系统的岩石学、年代学、元素地球化学、全岩Sr-Nd同位素研究,探讨其岩石成因及其构造意义.小九宫和沙店花岗岩的岩石类型主要为中粗粒斑状黑云二长花岗岩,LA-ICP-MS锆石U-Pb定年结果表明,其形成年龄分别为124±1 Ma和125±1 Ma,均为燕山晚期花岗岩.小九宫和沙店花岗岩均具有高钾、钙碱性、贫铁镁的含量特征,主要为弱过铝质花岗岩.两岩体具有相似的稀土元素分布型式和微量元素特征,表现为轻稀土富集的右倾型式,具有明显的Eu负异常（Eu/Eu*=0.17~0.50）,富集K、Rb、Th、U等大离子亲石元素,亏损Ba、Sr、P和高场强元素Nb、Ta、Ti等.主量、微量元素地球化学特征显示,两岩体为高钾钙碱性Ⅰ型花岗岩.小九宫和沙店花岗岩的ε_Nd（t）值分别为-8.06~-6.20、-6.51~-6.08,两阶段模式年龄（T_DM2）分别为1.42~1.57 Ga、1.42~1.45 Ga.Sr-Nd同位素组成和地球化学特征表明,两岩体主要来源于下地壳源区,其源岩可能为中元古代中性-基性火成岩.小九宫和沙店花岗岩体通过岩墙扩张作用方式被动侵位,结合区域构造背景,认为两岩体形成于伸展构造环境.地幔物质上涌可能为下地壳火成岩部分熔融提供持续的热源,岩浆在上升过程中经历明显的分离结晶作用.岩体中含有少量微粒包体及围岩捕虏体,反映岩浆在上升过程中可能受到较弱的混染作用.区域对比表明,从燕山早期到燕山晚期,赣西北-湘东北地区花岗质岩浆源区存在压力变小的趋势,可能反映了地壳的明显减薄.      

Oxidized, magnetite-series, rapakivi-type granites of Carajás, Brazil: Implications for classification and petrogenesis of A-type granites

The varying geochemical and petrogenetic nature of A-type granites is a controversial issue. The oxidized, magnetite-series A-type granites, defined by Anderson and Bender [Anderson, J.L., Bender, E.E., 1989. Nature and origin of Proterozoic A-type granitic magmatism in the southwestern United States of America. Lithos 23, 19–52.], are the most problematic as they do not strictly follow the original definition of A-type granites, and approach calc-alkaline and I-type granites in some aspects. The oxidized Jamon suite A-type granites of the Carajás province of the Amazonian craton are compared with the magnetite-series granites of Laurentia, and other representative A-type granites, including Finnish rapakivi and Lachlan Fold Belt A-type granites, as well as with calc-alkaline, I-type orogenic granites. The geochemistry and petrogenesis of different groups of A-types granites are discussed with an emphasis on oxidized A-type granites in order to define their geochemical signatures and to clarify the processes involved in their petrogenesis. Oxidized A-type granites are clearly distinguished from calc-alkaline Cordilleran granites not only regarding trace element composition, as previously demonstrated, but also in their major element geochemistry. Oxidized A-type granites have high whole-rock FeO_t/(FeO_t + MgO), TiO₂/MgO, and K₂O/Na₂O and low Al₂O₃ and CaO compared to calc-alkaline granites. The contrast of Al₂O₃ contents in these two granite groups is remarkable. The CaO/(FeO_t + MgO + TiO₂) vs. CaO + Al₂O₃ and CaO/(FeO_t + MgO + TiO₂) vs. Al₂O₃ diagrams are proposed to distinguish A-type and calc-alkaline granites. Whole-rock FeO_t/(FeO_t + MgO) and the FeO_t/(FeO_t + MgO) vs. Al₂O₃ and FeO_t/(FeO_t + MgO) vs. Al₂O₃/(K₂O/Na₂O) diagrams are suggested for discrimination of oxidized and reduced A-type granites. Experimental data indicate that, besides pressure, the nature of A-type granites is dependent of ƒO₂ conditions and the water content of magma sources. Oxidized A-type magmas are considered to be derived from melts with appreciable water contents (≥ 4 wt.%), originating from lower crustal quartz-feldspathic igneous sources under oxidizing conditions, and which had clinopyroxene as an important residual phase. Reduced A-type granites may be derived from quartz-feldspathic igneous sources with a metasedimentary component or, alternatively, from differentiated tholeiitic sources. The imprint of the different magma sources is largely responsible for the geochemical and petrological contrasts between distinct A-type granite groups. Assuming conditions near the NNO buffer as a minimum for oxidized granites, magnetite-bearing granites formed near FMQ buffer conditions are not stricto sensu oxidized granites and a correspondence between oxidized and reduced A-type granites and, respectively, magnetite-series and ilmenite-series granites is not always observed.     

Pre-eruptive conditions revealed by mega- and pheno-cryst compositions from the Quaternary Erzincan Volcanics, Eastern Turkey: Insights into the magma processes

Quaternary Erzincan Volcanics (QEVs) from the Erzincan Basin consist of mega- and pheno-cryst-bearing high-K calc-alkaline dome lavas. Fourteen nearly phenocrystic domes, with a range of basaltic-andesite, andesite, dacite and rhyolite compositions, were emplaced in the North Anatolian Fault Zone. The emplacement ages yielded by the unspiked K–Ar technique range from 102 to 140 ka. The andesitic domes (each less than 3 km in diameter) contain amphibole megacrysts. Amphibole compositions show a linear variation from ferro-edenite, edenite to pargasite from rhyolite to andesite. Pargasitic amphibole megacrysts scattered into the groundmass are very similar in composition to the microlites. All plagioclases are 53 mol%. Oscillation types are An₃₂₋₅₀ whose variations range from 10 to 16 mol% An and have 10–150 μm in thickness. Pre-eruptive conditions, calculated from mega- and pheno-cryst composition, using pyroxene and two oxide thermometers and the Al-in-hornblende barometer, ranged from 918 to 837 °C and 6.6 to 4.3 kbar for andesitic magma, 824–755 °C and 4.6–4.2 kbar for dacitic magma to 803–692 °C and 4.3–3.9 kbar for rhyolitic magma, which correspond to a depth of >10 km for storage region of the crust. The fO₂ values vary from −14.25 to −15.35 log units which are plotted just below nickel–nickel oxide (NNO) buffers. The systematic decrease in thermobarometric results from andesite to rhyolite is consistent with a single magma reservoir moving upward through the crust followed by fractional crystallization. Textural and compositional relationships of mega- and pheno-crystic phases suggest that magma mixing, fluid input to the reservoir and fractional crystallization processes, with a small amount crustal contamination play key role in evolution of the QEVs.     

Deformation-driven differentiation of granitic magma: the Stepninsk pluton of the Uralides, Russia

The wide compositional spectrum of the Variscan batholiths of the Urals, a continuum from gabbros (or diorites) to leucogranites, was produced by crystal fractionation, but the physical mechanisms involved in formation of the bodies remains obscure. To test whether syn-magmatic deformation was essential to enhance the efficiency of the process, we studied the Main Series of Stepninsk, a pluton emplaced into an active crustal-scale strike-slip shear zone. The Main Series (>95 vol.% of total granitoids) is high-K calc-alkaline, comprises rocks with SiO₂ from 51 to 77 wt.%, and stands out because most major and many trace elements yield excellent linear or curvilinear correlations with silica. It includes deformed gabbrodiorites to monzogranites, and undeformed syenogranites to alaskites. Deformed and undeformed rocks are coeval (283±2 Ma). All rocks, irrespective of their silica content, have the same initial Sr and Nd isotope ratios (⁸⁷Sr/⁸⁶Sr_{283 Ma}=0.70488±0.000131; ε(Nd)_{283 Ma}=−0.79±0.49), and contain amphibole and biotite with the same compositions. Based on thermodynamic and trace-element fractionation simulations, we propose a model of deformation-driven filter-pressing differentiation consistent with these features. The Main Series is derived from a hydrous high-K granodioritic magma which intruded containing 0.3 of early-formed solids. These accumulated locally by flow differentiation to produce the gabbrodiorites. The crystallization continued until the fraction of solids was higher than 0.55, after which different magma batches were efficiently squeezed by differential stress coupled with the opening of tensile fractures in the shear zone. This process produced a range of residua and segregates, the composition of which depended on the fraction of early-formed solids, the fraction of solids present when squeezing occurred and, especially, the efficiency of melt segregation. The monzodiorites and quartz–monzodiorites represent efficiently squeezed residua, the granodiorites to monzogranites represent unfractionated or little fractionated magma batches, and the leucogranites represent melt segregates with a few entrained crystals of amphibole and biotite. We proposed that wide-spectrum fractionation of granite magmas mainly occurs when they crystallize under compressive regimes, and is caused by deformation-driven filter-pressing differentiation.     

Source contributions to Devonian granite magmatism near the Laurentian border, New Hampshire and Western Maine, USA

Radiogenic isotope data (initial Nd, Pb) and elemental concentrations for the Mooselookmeguntic igneous complex, a suite of mainly granitic intrusions in New Hampshire and western Maine, are used to evaluate petrogenesis and crustal variations across a mid-Paleozoic suture zone. The complex comprises an areally subordinate monzodiorite suite [377±2 Ma; ε_Nd (at 370 Ma)=−2.7 to −0.7; initial ²⁰⁷Pb/²⁰⁴Pb=15.56–15.58] and an areally dominant granite [370±2 Ma; ε_Nd (at 370 Ma)=−7.0 to −0.6; initial ²⁰⁷Pb/²⁰⁴Pb=15.55–15.63]. The granite contains meter-scale enclaves of monzodiorite, petrographically similar to but older than that of the rest of the complex [389±2 Ma; ε_Nd (at 370 Ma)=−2.6 to +0.3; initial ²⁰⁷Pb/²⁰⁴Pb 15.58, with one exception]. Other granite complexes in western Maine and New Hampshire are 30 Ma older than the Mooselookmeguntic igneous complex granite, but possess similar isotopic signatures.

Derivation of the monzodioritic rocks of the Mooselookmeguntic igneous complex most likely occurred by melting of Bronson Hill belt crust of mafic to intermediate composition. The Mooselookmeguntic igneous complex granites show limited correlation of isotopic variations with elemental concentrations, precluding any significant presence of mafic source components. Given overlap of initial Nd and Pb isotopic compositions with data for Central Maine belt metasedimentary rocks, the isotopic heterogeneity of the granites may have been produced by melting of rocks in this crustal package or through a mixture of metasedimentary rocks with magmas derived from Bronson Hill belt crust.

New data from other granites in western Maine include Pb isotope data for the Phillips pluton, which permit a previous interpretation that leucogranites were derived from melting heterogeneous metasedimentary rocks of the Central Maine belt, but suggest that granodiorites were extracted from sources more similar to Bronson Hill belt crust. Data for the Redington pluton are best satisfied by generation from sources in either the Bronson Hill belt or Laurentian basement. Based on these data, we infer that Bronson Hill belt crust was more extensive beneath the Central Maine belt than previously recognized and that mafic melts from the mantle were not important to genesis of Devonian granite magma.     

Temporal variation of mineralogy and petrology in cognate gabbroic enclaves at Arenal volcano,Costa Rica

Gabbroic enclaves ejected during the current eruption phase (A-1) and during the latest prehistoric eruption phase (A-2) of Arenal Volcano show systematic variations in texture, mineralogy and composition as a function of host rock chemistry and timing of eruption. The most differentiated enclaves occur in the more differentiated A-2 lavas. Enclaves in the A-1 volcanics are consistently less evolved. Within the current A-1 eruption, the most mafic enclaves are amphibole-bearing rocks that were erupted during the first 2–3 years of activity (1968–1970). These enclaves occur in the most differentiated A-1 volcanics and are not in equilibrium with their host rocks. They crystallized from a hydrous melt that was slightly more mafic than anything erupted during the current cycle. We interpret the enclaves as sidewall crystallization products of a melt, possibly a high-alumina basalt, that was immediately parental to the A-1 lavas. Enclaves that occur in A-1 rocks erupted after 1970 and all of the A-2 enclaves are amphibole-free and less mafic than the early A-1 enclaves. Their chemistry suggests that they formed during the early to intermediate crystallization of their host lavas. None of the enclaves contain minerals that might have equilibrated with a primary, mantle-derived melt. Geothermometry is consistent with geochemistry, with amphibole-bearing A-1 enclaves yielding the highest pyroxene temperatures (ave. 1090° C) and A-2 enclaves the lowest (ave. 1030° C). Geobarometry suggests mid- to upper crustal depths for the crystallization of all enclaves. The enclaves are cognate and reflect pre-eruptive crystallization of Arenal magmas. They record evolution from a hydrous, basaltic magma to the drier basaltic andesites that characterize the current eruption. Volatiles appear to have been lost due to depressurization during the slow ascent of the magmas through the upper levels of the crust following the initial explosive eruption. Volatile loss and depressurization resulted in the destabilization and the progressive resorption of amphibole. The A-2 lavas may represent the long-term fractionation products of basaltic andesite magmas similar in composition to the A-1 lavas. Anorthitic plagioclase, commonly thought of as a phase stabilized by high Ca/Na and high water pressure, continued to crystallize in a system with relatively low Ca/Na and which had dehydrated and/or depressurized to the point at which amphibole was no longer stable. This suggests that compositional characteristics other than high Ca/Na or high water content may have stabilized the anorthite in the basaltic and basaltic andesite melts at Arenal. We speculate that the high-alumina content of the Arenal magmas may be the stabilizing factor.     

Petrological and geochronological constraints on the origin of the Palimé–Amlamé granitoids (South Togo, West Africa): A segment of the West African Craton Paleoproterozoic margin reactivated during the Pan-African collision

The Palimé–Amlamé Pluton (PAP) in southern Togo, consists of silica-rich to intermediate granitoids including enclaves of mafic igneous rocks and of gneisses. They are commonly called the “anatectic complex of Palimé–Amlamé” and without any convincing data, they were interpreted either as synkinematic Pan-African granitoids or as reworked pre Pan-African plutons. New field and petrological observations, mineral and whole-rock chemical analyses together with U–Pb zircon dating, have been performed to evaluate the geodynamic significance of the PAP within the Pan-African orogenic belt. With regard to these new data, the granitoids and related enclaves probably result from mixing and mingling processes between mafic and silicic magmas from respectively mantle and lower crust sources. They display Mg–calc-alkaline chemical features and present some similarities with Late Archaean granites such as transitional (K-rich) TTGs and sanukitoids.

The 2127 ± 2 Ma age obtained from a precise U/Pb concordia on zircon, points out a Paleoproterozoic age for the magma crystallization and a lower intercept at 625 ± 29 Ma interpreted as rejuvenation during Pan-African tectonics and metamorphism. Based on these results, a Pan-African syn to late orogenic setting for the PAP, i.e. the so-called “anatectic complex of Palimé–Amlamé”, can be definitively ruled out. Moreover according to its location within the nappe pile and its relationships with the suture zone, the PAP probably represents a fragment of the West African Craton reactivated during the Pan-African collision.     

Mineral chemistry constraints on the evolution of the 1.88–1.87 Ga post-kinematic granite plutons in the Central Finland Granitoid Complex

A suite of post-kinematic, 1.88–1.87 Ga, silicic plutons crosscut 1.89–1.88 Ga synkinematic granitoids in the Central Finland Granitoid Complex (CFGC) in south-central Finland. The plutons range from biotite±hornblende quartz monzonite to syenogranite and include pyroxene- and olivine-bearing varieties. Mineral chemical data on feldspars, biotite, amphibole, pyroxenes, olivine, and oxides of the post-kinematic plutons are presented. The data are interpreted to show that these plutons register (1) a considerable range in pressure from 2–4 kbar (amphibole barometry) to 5–7 kbar (olivine–pyroxene barometry), (2) temperatures mostly reflecting resetting during cooling (450–800°C; QUIlF thermometry), and (3) low fO₂ (log fO₂ ΔFMQ −0.3 to −1.5; QUIlF equilibria). In particular, plutons with olivine- and pyroxene-bearing margins and amphibole-dominated central parts record progressive oxidation and hydration upon cooling, shifting from the QUIlF equilibrium toward KUIlB. The post-kinematic granites can be considered post-collisional in regard to compressional events in the CFGC and display many of the characteristics of the anorogenic 1.6 Ga rapakivi granites further south. They were presumably derived from a deep and dry crustal source, like the rapakivi granites.     

Crystal fractionation in the petrogenesis of an alkali monzodiorite–syenite series: the Oshurkovo plutonic sheeted complex, Transbaikalia, Russia

The Oshurkovo Complex is a plutonic sheeted complex which represents numerous successive magmatic injections into an expanding system of subparallel and subvertical fractures. It comprises a wide range of rock types including alkali monzodiorite, monzonite, plagioclase-bearing and alkali-feldspar syenites, in the proportion of about 70% mafic rocks to 30% syenite. We suggest that the variation within the complex originated mainly by fractional crystallization of a tephrite magma.

The mafic rocks are considered as plutonic equivalents of lamprophyres. They exhibit a high abundance of ternary feldspar and apatite, the latter may attain 7–8 vol.% in monzodiorite. Ternary feldspar is also abundant in the syenites. The entire rock series is characterized by high Ba and Sr concentrations in the bulk rock samples (3000–7000 ppm) and in feldspars (up to 1 wt.%). The mafic magma had amphibole at the liquidus at 1010–1030 °C based on amphibole geothermometer. Temperatures as low as this were due to high H₂O and P₂O₅ contents in the melt (up to 4–6 and 2 wt.%, respectively). Crystallization of the syenitic magmas began at about 850 °C (based on ternary feldspar thermometry). The series was formed at an oxygen fugacity from the NNO to HM buffer, or even higher.

The evolution of the alkali monzodiorite–syenite series by fractional crystallization of a tephritic magma is established on the basis of geological, mineralogical, geochemical and Sm–Nd and Rb–Sr isotope data. The geochemical modeling suggests that fractionation of amphibole with subordinate apatite from the tephrite magma leaves about 73 wt.% of the residual monzonite melt. Further extraction of amphibole and plagioclase with minor apatite and Fe–Ti oxides could bring to formation of a syenite residuum. Rb–Sr isotopic analyses of biotite, apatite and whole-rock samples constrain the minimum age of basic intrusions at ca. 130 Ma and that of cross-cutting granite pegmatites at ca. 120 Ma. Hence the entire evolution took place in an interval of ≤10 My. Initial ⁸⁷Sr/⁸⁶Sr ratios for the mafic rocks range from 0.70511 to 0.70514, and for syenites from 0.70525 to 0.70542. Initial _Nd (130 Ma) values for mafic rocks vary from −1.9 to −2.4, and for syenites from −2.9 to −3.5. In a _Nd(T) vs. (⁸⁷Sr/⁸⁶Sr)_i diagram, all rock types of the complex fall in the enriched portion of the Mantle Array, suggesting their derivation from a metasomatized mantle source. However, the small but distinguishable difference in Sr and Nd isotopic compositions between mafic rocks and syenites probably resulted from mild (10–20%) crustal contamination during differentiation. Large negative Nb anomalies are interpreted as a characteristic feature of the source region produced by Precambrian fluid metasomatism above a subduction zone rather than by crustal contamination.     

Isotopic equilibrium/disequilibrium in granites, metasedimentary rocks and migmatites (Damara orogen, Namibia)—a consequence of polymetamorphism and melting

The overwhelming part of the continental crust in the high-grade part of the Damara orogen of Namibia consists of S-type granites, metasedimentary rocks and migmatites. At Oetmoed (central Damara orogen) two different S-type granites occur. Their negative ε_Nd values (− 3.3 to − 5.9), moderately high initial ⁸⁷Sr/⁸⁶Sr ratios (0.714–0.731), moderately high ²⁰⁶Pb/²⁰⁴Pb (18.21–18.70) and ²⁰⁸Pb/²⁰⁴Pb (37.74–37.89) isotope ratios suggest that they originated by melting of mainly mid-Proterozoic metasedimentary material. Metasedimentary country rocks have initial ε_Nd of − 4.2 to − 5.6, initial ⁸⁷Sr/⁸⁶Sr of 0.718–0.725, ²⁰⁶Pb/²⁰⁴Pb ratios of 18.32–18.69 and ²⁰⁸Pb/²⁰⁴Pb ratios of 37.91–38.45 compatible with their variation in Rb/Sr, U/Pb and Th/Pb ratios. Some migmatites and residual metasedimentary xenoliths tend to have more variable ε_Nd values (initial ε_Nd: − 4.2 to − 7.1), initial Sr isotope ratios (⁸⁷Sr/⁸⁶Sr: 0.708–0.735) and less radiogenic ²⁰⁶Pb/²⁰⁴Pb (18.22–18.53) and ²⁰⁸Pb/²⁰⁴Pb (37.78–38.10) isotope compositions than the metasedimentary rocks. On a Rb–Sr isochron plot the metasedimentary rocks and various migmatites plot on a straight line that corresponds to an age of c. 550 Ma which is interpreted to indicate major fractionation of the Rb–Sr system at that time. However, initial ⁸⁷Sr/⁸⁶Sr ratios of the melanosomes of the stromatic migmatites (calculated for their U–Pb monazite and Sm–Nd garnet ages of c. 510 Ma) are more radiogenic (⁸⁷Sr/⁸⁶Sr: 0.725) than those obtained on their corresponding leucosomes (⁸⁷Sr/⁸⁶Sr: 0.718) implying disequilibrium conditions during migmatization that have not lead to complete homogenization of the Rb–Sr system. However, the leucosomes have similar Nd isotope characteristics than the inferred residues (melanosomes) indicating the robustness of the Sm–Nd isotope system during high-grade metamorphism and melting. On a Rb–Sr isochron plot residual metasedimentary xenoliths show residual slopes of c. 66 Ma (calculated for an U–Pb monazite age of 470 Ma) again indicating major fractionation of Rb/Sr at c. 540 Ma. However, at 540 Ma, these xenoliths have unradiogenic Sr isotope compositions of c. 0.7052, indicating depleted metasedimentary sources at depth. Based on the distinct Pb isotope composition of the metasedimentary rocks and S-type granites, metasedimentary rocks similar to the country rocks are unlikely sources for the S-type granites. Moreover, a combination of Sr, Nd, Pb and O isotopes favours a three-component mixing model (metasedimentary rocks, altered volcanogenic material, meta-igneous crust) that may explain the isotopic variabilty of the granites. The mid-crustal origin of the different types of granite emphasises the importance of recycling and reprocessing of pre-existing differentiated material and precludes a direct mantle contribution during the petrogenesis of the orogenic granites in the central Damara orogen of Namibia.     

湘中紫云山岩体暗色微粒包体的成因:岩相学、全岩及矿物地球化学证据

暗色微粒包体广泛分布于湘中紫云山岩体中的似斑状角闪石黑云母花岗闪长岩中,但其研究程度较低.对具有火成结构的暗色微粒包体及其寄主岩进行了岩相学、全岩及长石、辉石、黑云母的矿物地球化学研究,探讨其岩石成因及构造意义.寄主岩的全岩主量、微粒元素较为均一,而暗色微粒包体变化较大,且后者相对贫SiO₂而富Na₂O,但总体上二者均具有准铝质、钙碱性、镁质的特征,均富集轻稀土和大离子亲石元素,而亏损重稀土和高场强元素.寄主岩和暗色微粒包体的斜长石、辉石和黑云母均分别属于中长石、次透辉石－低铁次透辉石和铁质黑云母的范畴,显示相似的矿物地球化学特征.详尽的岩相学和地球化学特征表明,寄主岩属于I型和ACG型花岗岩,具有明显壳幔混合的特点;而暗色微粒包体形成时处于液态并具有流动性,与寄主岩间存在明显的机械和化学混合作用,并具有早期为骤冷快速结晶、晚期缓慢结晶这两期过程.因此,紫云山岩体中出现大量暗色微粒包体,是印支晚期湘中地区在强烈挤压之后的松弛阶段,由于软流圈物质上涌,并与其诱发的壳源酸性岩浆混合作用的产物.      

藏北尼玛地区白垩纪岩浆岩对班公湖-怒江缝合带演化的制约

班公湖-怒江缝合带及其两侧广泛分布白垩纪岩浆岩,这些岩浆活动记录了班公湖-怒江特提斯洋俯冲至闭合以及拉萨-羌塘板块碰撞过程.为了约束该缝合带在早-晚白垩世的演化过程,本文对缝合带中段尼玛地区花岗岩进行岩相学、地球化学、锆石年代学和Hf同位素研究.尼玛北部虾别错花岗岩侵入到中生代地层中,发育石英闪长质包体.锆石U-Pb定...     

Fluid-bearing alkaline carbonate melts as the medium for the formation of diamonds in the Earth''s mantle: an experimental study

We have experimentally studied the formation of diamonds in alkaline carbonate–carbon and carbonate–fluid–carbon systems at 5.7–7.0 GPa and 1150–1700 °C, using a split-sphere multi-anvil apparatus (BARS). The starting carbonate and fluid-generating materials were placed into Pt and Au ampoules. The main specific feature of the studied systems is a long period of induction, which precedes the nucleation and growth of diamonds. The period of induction considerably increases with decreasing P and T, but decreases when adding a C–O–H fluid to the system. In the range of P and T corresponding to the formation of diamonds in nature, this period lasts for tens of hours. The reactivity of the studied systems with respect to the diamond nucleation and growth decreases in this sequence: Na₂CO₃–H₂C₂O₄·2H₂O–C>K₂CO₃–H₂C₂O₄·2H₂O–C>>Na₂CO₃–C>K₂CO₃–C. The diamond morphology is independent of P and T, and is mainly governed by the composition of the crystallization medium. The stable growth form is a cubo-octahedron in the Na₂CO₃ melt, and an octahedron in the K₂CO₃ melt. Regardless of the composition of the carbonate melt, only octahedral diamond crystals formed in the presence of the C–O–H fluid. The growth rates of diamond varied in the range from 1.7 μm/h at 1420 °C to 0.1–0.01 μm/h at 1150 °C, and were used to estimate, for the first time, the possible duration of the crystallization of natural diamonds. From the analysis of the experimental results and the petrological evidence for the formation of diamonds in nature, we suggest that fluid-bearing alkaline carbonate melts are, most likely, the medium for the nucleation and growth of diamonds in the Earth's upper mantle.