Fractional Crystallization Processes Research Articles

Processes controlling magma fertility at buenavista del cobre porphyry copper deposit (cananea, méxico): A new petrogenetic model based on zircon u-pb dating and apatite geochemistry

The Buenavista del Cobre is a world-class porphyry Cu-Mo deposit located in the Cananea Mining District, northern Sonora, México. Using zircon U-Pb dating, we show that the Proterozoic Cananea Granite, unconformably overlain regionally by Paleozoic limestones hosting skarn deposits underlies the present-day pit. We also present new crystallization ages for host rocks of copper mineralization in the District, dating for the first time a volcanic rock of the Henrietta Formation at 186.8 ± 1.1/3.0 Ma and the El Torre Syenite at 176.3 ± 1.1/2.9 Ma. Zircon U-Pb dating of the different porphyritic bodies reveals that the magmatic activity at Buenavista del Cobre lasted at least 4 Myr, from 59.7 ± 0.5/1.1 Ma to 56.1 ± 0.2/0.9 Ma. The deposit is composed by several porphyry intrusions referred to as “ore-rich” and “ore-poor” based on their individual metal contributions, which provides the opportunity to study the origin and processes enhancing magma fertility in an individual deposit. Combining our new geochronological dataset with geochemistry of apatite from the different porphyries allows us to propose a new petrogenetic model for the Buenavista del Cobre deposit. As the apatite Eu and Ce anomalies overlap with no clear difference between the ore-rich and ore-poor intrusions, we propose that the magmatic oxidation states of the magmas were similar. However, differences in apatite REE signatures, as well as variations in apatite Sr compositions between the two groups suggest that fractional crystallization processes in the parental magma influence the fertility of the porphyries. Additionally, apatite Cl contents of ore-rich porphyry intrusions are higher (>0.4 wt%) than the ore-poor intrusions (<0.2 wt%), suggesting an important role of the initial Cl content of the magmas in the mineralization process. These observations give new insights on the petrogenetic processes at origin of porphyry magma fertility. We propose that the evolution of the parental melt by fractional crystallization of hydrous minerals (hornblende) at upper crustal levels induced low H2O content of the residual magma, resulting in the formation of ore-poor porphyries. In contrast, we suggest that fractionation of anhydrous minerals (plagioclase) increased the H2O content in the residual melt, leading to the formation of ore-rich porphyries. Our new data allow us to propose an original genetic model for the Buenavista del Cobre deposit, which involves two cycles of supply, cooling and partial crystallization. This contribution shows that petrogenetic processes controlling porphyry copper magmas fertility are recorded in the composition of apatite at the deposit scale and highlights the importance of considering apatite geochemistry as an exploration tool.

On the coexistence of rift-related silica-undersaturated and silica-saturated alkaline rocks – The cretaceous Messum alkaline complex (Namibia) revisited

The ~132 Ma-old Messum igneous complex, a circular structure of ~18 km diameter, belongs to the Damaraland intrusive complexes that intruded into the Pan-African Damara basement of Namibia. The plutonic rocks of the core of the complex comprise olivine-gabbro, biotite-gabbro, nepheline-syenite and quartz-syenite as well as minor alkali gabbro and coexist with the Etendeka volcanic sequences of the Goboboseb Mountains, comprising basalts (Tafelkop and Tafelberg types) that are overlain by deposits of several quartz latite eruptions. New major and trace element and Sr, Nd and Pb isotope data are reported for nepheline-syenite and quartz-syenite. Major and trace element data are consistent with the development of nepheline-syenites through fractional crystallization processes. The nepheline-syenite samples have initial 87Sr/86Sr of 0.7046–0.7049 and initial εNd ranging from +0.53 to +1.47, indicating a mantle source with time-integrated lithophile element depletion. Initial Pb isotopes are rather uniform (206Pb/204Pb:17.89–18.14, 207Pb/204Pb: 15.56–15.58, 208Pb/204Pb: 37.78–38.00). Uniform initial Sr and Pb isotope ratios for nepheline-syenites suggest that the syenite magmas evolved through fractional crystallization from an inferred mafic alkaline magma without crustal contamination. However, the range in Nd isotope composition is too large to be related to crystal fractionation alone and imply a heterogeneous source with respect to the Nd isotope composition. The quartz-syenites show a large range in initial εNd (+1.0 to −4.4) and initial 87Sr/86Sr (0.7047–0.7115). Initial Pb isotope ratios are also heterogeneous (206Pb/204Pb: 18.29–18.74, 207Pb/204Pb: 15.60–15.65, 208Pb/204Pb: 37.43–38.49). These data, together with major and trace element constraints and results from AFC modeling substantiate the production of the quartz-syenites by fractional crystallization of clinopyroxene, amphibole and K-feldspar accompanied by assimilation of up to about 30 % pre-Pan African lower crust. Isotope and chemical data do not support derivation from a single batch of magma undergoing contamination, but suggest that a large magma body at depth evolved largely by fractionation with batches of melt extracted from this chamber being variably contaminated at lower crustal levels.

Constraints of upper crust magmatic processes on the formation of Saindak porphyry Cu deposit: Insights from mineral geochemistry

Upper crustal magmatic processes play a crucial role in linking the magmatic and hydrothermal systems of porphyry deposits, ultimately controlling the generation of ore-forming fluids. Understanding these processes within a magma chamber is essential for deciphering the formation of porphyry deposits. The Saindak deposit, a large porphyry Cu system in the western Chagai belt, features coeval ore-forming and barren magma pulses, providing key insights into the characterization of porphyry systems. In this study, detailed petrographic observations and geochemical analyses of amphibole, plagioclase, and apatite were conducted to unravel the magmatic evolution at Saindak. Based on textural relationships and crystallization sequences, three distinct populations of amphibole in the ore-forming magma were identified. These amphiboles record the entire fractional crystallization process of magma that initially emplaced at a depth of ∼5 km to the connected magma system at ∼2 km. The study of amphibole and apatite reveals that the fertile magma underwent large-scale fluid exsolution in an open system. The simultaneous and rapid depletion of Cu, Cl, S, and H2O in the magma indicates that Cl and S were highly partitioned into the exsolved fluid phase. These elements formed complexes, which effectively concentrated metals in the fluid. Conversely, the barren magma was characterized by either low metal content or limited fluid exsolution within the magma chamber. Overall, we reconstruct the upper crustal magmatic processes at Saindak and conclude that efficient extraction of Cu through fluid exsolution is the key to porphyry deposit formation.

A Trachytic Monogenetic Volcano in the Changbaishan Volcanic Field, Xitudingzi Volcano: Petrogenesis, Magma Plumbing System and Implications for Non-basaltic Monogenetic Volcanism

Abstract The Changbaishan volcanic field is the largest Quaternary volcanic field in China and includes the most dangerous polygenetic volcano, Tianchi volcano. In addition to the Tianchi volcano, the Changbaishan volcanic field contains two other polygenetic volcanoes (Wangtian’e volcano and Namphothe volcano) and at least 150 monogenetic volcanoes. The compositions of these monogenetic volcanoes range from basalt to rhyolite. Basaltic monogenetic volcanoes are the most abundant and spread throughout the volcanic field, whereas intermediate to evolved monogenetic volcanoes are found only within the Touxi subfield. We know very little about these non-basaltic monogenetic volcanoes, especially the magmatic petrogenesis, volcanological origins and structure of the magma plumbing system beneath them. Therefore, in this study, the Xitudingzi volcano within the Touxi subfield is used as an example to study the petrogenesis of silicic magma and explore the structure of the magma system by combining new 40Ar/39Ar dating, whole-rock geochemistry, Sr-Nd isotopes, and mineral chemistry. The 40Ar/39Ar chronology results showed that the Xitudingzi volcano erupted at 1.17 Ma; this volcano is younger than the other monogenetic volcanoes in the Touxi subfield. The geochemical results indicated that the eruption products of the Xitudingzi volcano are trachytic and formed from the assimilation fractional crystallization (AFC) process of an alkaline basaltic parental magma. The results from the Rhyolite-MELTS and thermobarometry indicated that the magma plumbing system of the Xitudingzi volcano contained two magma chambers at depths of 8 km and 19 km, respectively. The trachytic magma of Xitudingzi was produced by the AFC process from the alkaline basaltic magmas in the deep magma chamber and then transported to the shallow magma chamber. Furthermore, differences in the trace element concentrations between the different units of the Xitudingzi volcano indicated that the shallow pre-eruptive magma chamber was compositionally zoned. Based on the results from our study, the upper crustal magma plumbing system of the Xitutingzi volcano existed independently of the magma plumbing system of the cone-construction stage of the Tianchi volcano, even though the two volcanoes had similar ages of activity as well as the same chemical composition of eruptive products. Based on these results and other existing studies, a relatively thick crust and the developed faults are likely the key factors for the formation of intermediate to evolved monogenetic volcanos in the Touxi volcanic field.

New bulk rock and age data on the changes in magma evolution during the Miocene, Galatean volcanic area, central Anatolia, Turkey: A review

The Galatean Volcanic Province (GVP) lies within the Sakarya tectonic belt in the northwest of central Anatolia, Turkey, south of the North Anatolian Fault, cropping out over 12,000 km2. It consists of Early Miocene intermediate to acid lavas, pyroclastic rocks, volcaniclastic deposits, and Late Miocene OIB-like basalts. Our study is based on new bulk geochemistry, SrNd isotopes, and 40Ar/39Ar dating of the volcanic rocks from the south-western part of GVP, but integrates all the available previous data to understand how magmas evolved in the post-collisional geodynamic condition in the GVP. The initial eruptions were rhyolitic, as domes or pyroclastic deposits (Group 1) and basaltic lavas (Group 2) during the Early Miocene. Group 2 is also represented by large volumes of basaltic-andesitic, trachyandesite-dacite/trachydacite lava flows, small intrusions, and pyroclastic deposits as generated between 21 and 14 Ma. Relatively low 87Sr/86Sr ratios (0.705–0.706) of the early rhyolites (Group 1), similar to all the rocks from Group (2), suggest the generation of hybrid melts with variable contributions of mantle-derived and crustal material. The volcanic activity ends with OIB-like basalts (11–7 Ma) showing the lowest 87Sr/86Sr (∼0.703) suggesting an asthenospheric origin.The geodynamic model, based on post-Cyprian slab rollback, results in long-term (22–13 Ma) post-collisional delamination/drip processes that support magmatism. This magmatism is generated in the lithospheric mantle, with the formation of basaltic melts and acid hybrid melts showing variable contributions of mantle-derived and crustal materials in a complex trans-crustal magma plumbing system. Complex mixing of various intra-crustal magmas and fractional crystallization processes generated a huge volume of volcanic rocks. The Late Miocene small-volume OIB basalts were asthenospheric melts that during the late stage recorded localized decompression melting processes.

Nd-isotope effects through factional crystallisation-assimilation (AFC) processes in the continental crust, heterogeneous in age: the example of ferrobasalts from the Ladoga Graben (Karelia, Russia)

Petrography, geochemistry and isotope geochemistry of the Mesoproterozoic volcanic rocks occurred as lava flows and the Valaam sill in the Ladoga rift, have been studied. The Ladoga rift is located in the area of thrusting of the Palaeoproterozoic Svekofennian orogenic complexes onto the Archean Karelian craton. Ferrobasites of close composition and geological position in lava flows and sill have different Nd isotopic composition, differing by 5 units εNd(t): –4…-5 in ferrobasalts of lava flows and a very low-radiogenic Nd isotopic composition in mafic rocks of the sill (εNd(t) to –11 for ferrogabbro), and identical to the isotopic composition of its acidic rocks (εNd(t) to –11 for granophyres). It is shown that in the crust, heterogeneous in age, the process of fractional crystallisation along the tholeiitic trend combined with assimilation of melt from wall rocks can be an effective mechanism for forming such “paradoxical” features of the Nd isotopic composition. The isotopic composition of sill rocks indicates the probable presence of Mesoarchean blocks in the lower crust of the Ladoga graben region.

Magma mingling in plagiogranites of the Oman ophiolite suggests an origin by fractional crystallisation

Late-stage plagiogranites in the Oman-UAE ophiolite are frequently associated with layered and massive gabbro bodies, intrusive into the mid-crustal section of the ophiolite. This study reports persuasive field evidence from five different localities for magma-mingling between plagiogranites and melts with a mafic and dioritic composition. It is argued from these relationships that mafic and felsic magmas coexisted in the same magma chamber. On this basis it is suggested that the range of melt compositions is related by a process of fractional crystallisation. The plagiogranites are interpreted as the end-product of this fractionation process and the associated gabbros are thought to be related cumulates. The hypothesis is supported with geochemical evidence which shows from the major element chemistry a continuum of compositions between the most mafic and felsic endmembers (47.6–80.6 wt% SiO2). These compositions ‘capture’ the fractionation process in operation. Modelling these variations using the major and trace element chemistry indicates that the fractionating assemblage comprised olivine-clinopyroxene-plagioclase+/−amphibole and that some plagiogranites contained cumulus plagioclase. The mafic rocks associated with late stage plagiogranite formation are derived from a highly depleted mantle source, which implies melting of an already-depleted mantle. This is consistent with previous models for the origin of the Oman ophiolite and implies a supra-subduction setting for this phase of ocean crust evolution in this ophiolite.

Genesis of the Jiada pegmatite lithium deposit in the Ke’eryin ore field, western Sichuan, China: Evidence from whole-rock trace element and Li isotope

The origin and petrogenesis of pegmatite-type lithium deposits within the Songpan-Garze Fold Belt (SGFB) of western China remain subjects of debate. To provide further insight on this subject, this study investigated the whole-rock trace elements and whole-rock Li isotopic compositions of the two-mica monzogranite (TMG) from the Ke’eryin composite pluton, the Jiada albite pegmatite (AP) and albite-spodumene pegmatite (ASP) and their metasedimentary wall rocks within the Ke’eryin ore field in the eastern SGFB. Modeling of muscovite-dehydration melting based on the whole-rock trace elements (e.g., Li, Rb, and Sr) and Rayleigh dehydration modeling related to the whole-rock Li isotopes suggest that the Jiada pegmatites are unlikely to have originated from the low-degree partial melting of metasandstone (MS) of the Zhuwo Formation. Variations in the whole-rock trace elements and Li isotope between the TMG and the Jiada pegmatites are consistent with the evolution trend of magmatic fractionation. However, the whole-rock Li isotopic compositions of the AP and ASP display inverse variation characteristics with the muscovite Li isotopic compositions, with the AP exhibiting lower Li concentrations and higher whole-rock δ7Li values than ASP. Furthermore, the variation patterns of whole-rock trace elements do not align perfectly with the Rayleigh-type fractional crystallization processes, implying other geological processes would be also involved in the formation of the Jiada pegmatites. Collectively considering the Li isotope behavior during various geological processes, the observed variations in whole-rock Li isotopic compositions between AP and ASP can be explained by aqueous fluid enrichment during the pegmatitic melt evolution. This suggests that fractional crystallization and fluid exsolution jointly contributed to pegmatite formation and Li mineralization in the Jiada deposit. Moreover, the whole-rock δ7Li values of the wall rock of ASP (MS2) are lower than those of MS and the wall rock of ASP (MS1), primarily due to metasomatism by 6Li-enriched fluids expelled from ASP and the kinetic diffusion of Li isotopes. The high concentrations of highly mobile elements, especially Li and Cs, combined with the low whole-rock δ7Li value of the metasandstone, could serve as effective tracers for locating concealed orebodies and evaluating the metallogenic potential of Li mineralization.

Petrogenesis of a TTG intrusive suite: the La Dauversière pluton, Abitibi greenstone belt, Canada

Insights into the source and partial melting conditions of tonalite–trondhjemite–granodiorite (TTG) intrusive suites provide essential constraints on the tectonic regimes prevailing before 2.5 Ga. As case studies on individual suites increase, the TTG group becomes more heterogeneous, offering detailed insights into the evolution of the Archean crust. This study focuses on the La Dauversière pluton, a TTG suite in the Chibougamau area, Abitibi greenstone belt, Canada, to unravel complex differentiation processes in a pluton with a relatively limited volume. According to whole-rock and zircon chemistry, the La Dauversière pluton is a TTG suite that contains less Na and light rare earth elements (LREE) than other TTG suites of the Abitibi greenstone belt. Whole-rock chemistry and melt inclusions in zircon also point to an atypical fractional crystallization process that favors K enrichment, contrasting with the Na enrichment trends observed in most TTG suites globally. Magma hybridization, with late magma pulses interacting with early phases partially crystallized at depth, likely explains the chemistry of the La Dauversière pluton. The source of these magmas differs from the basaltic source that gave rise to most TTG suites of the Abitibi greenstone belt, possibly because older basement occurs in the Chibougamau area and is lacking in the rest of the greenstone belt. The La Dauversière pluton underscores the importance of interpreting the petrogenesis of individual TTG suites before inferring global source processes and geodynamic settings.

Chemical constraints and tectonic setting of the Ginebra ophiolite complex

The occurrence and types of ophiolites in the Central Cordillera of the Colombian Andes have not been identified in terms of their tectonic settings and geochemical features. Therefore, the study of the tectonic setting and subduction zones in the ophiolites’ magmatic evolution becomes a significant issue. The Ginebra Ophiolitic Complex (GOC) is located on the western flank of the Central Cordillera in the Valle del Cauca Department, southwest of Colombia, assigned to the Lower Cretaceous period, as indicated by the contact of the GOC with the Buga Batholith. The GOC is formed by three main lithologies: amphibolite, gabbro, and ultramafic rocks (pyroxenite and peridotite), according to Ossa (2007). The rocks in the Puente Piedra section, located in the northeast of Ginebra municipality, are part of the gabbroic cumulates within the ophiolitic sequence. This sequence comprises interspersed layers of gabbroic cumulates, gabbrodiorites, and diorites; interpreted as a result of crystal accumulation and fractional crystallization processes. The mafic rocks of the GOC are sub-alkaline and correspond to the low potassium (K2O wt% 0.03-0.06) tholeiitic series. Geochemically, they have SiO2 wt% ranging from 49 to 61 and an aluminum oxide saturation index of approximately ~0.4 and ~0.8, indicating a metaluminous type. The geochemistry of the studied rocks from Puente Piedra section indicates that the GOC formed through fractional crystallization and accumulation processes from a single magma source. Cluster analysis, used to compare the geochemistry of GOC rocks and the Amaime Complex basalts, suggests a similar magma source, possibly linked to multiple recharge events that underwent fractional crystallization, melt extraction, and accumulation processes. The geochemical parameters are indicative of a suprasubduction zone ophiolite, characterized by a low potassium tholeiitic series affinity, TiO2 values typically &lt;1.2 wt%, Th enrichment typical of subduction zones, high Pb content, and low values of Ti, Y, Yb, Ta, Nb, Zr, and Hf.

Geochemistry, Rb-Sr whole rock age and Sr-Nd isotopic constraints on the Variscan A1-type granite from Azegour area in the Marrakech High Atlas (Moroccan Meseta) and their geodynamic implications

In the northern part of the Marrakech High Atlas (MHA), along the southern Variscan segment of the Western Meseta, a Variscan granitic intrusion crops out, intruding metasediments and meta-volcanosedimentary rocks of Early Cambrian to Ordovician age. A new whole-rock Rb-Sr isochron age of 268 ± 9 Ma for the granite, combined with a previously published whole-rock Rb-Sr radiometric dating (271 ± 3 Ma), reveals a post-kinematic (tectonic) character with regard to the main Variscan deformational event, belonging within the tectonic context of the Moroccan Variscan orogenic belt. Geochemically, the Azegour intrusion is metaluminous to peraluminous and exhibits a calc-alkaline affinity with a ferruginous composition. The massif shows an extremely differentiated character (SiO2 = 77.53–78.14 per cent), K2O and high total alkali contents, FeOt/(FeOt + MgO) and Ga/Al ratios, which have typical characteristics of an A-type granite. In addition, the granite contains high concentrations of LREE (LaN/SmN= 7.9–13.67) relative to HREE (LaN/YbN= 4.81–11.61) and a well-defined Eu negative anomaly (Eu/Eu* = 0.44–0.75). The granitic samples exhibit a strong enrichment of the most incompatible elements (RbN/YbN = 69.84–159.98) and a strong depletion of Ba, Sr, Eu, Nb, P and Ti. These characteristics are similar to those of A1-type granites. The absence of mineralogy typical of an S-type granite, combined with its weakly peraluminous character [A/CNK (molar Al2O3/CaO+Na2O+K2O) = 1,013–1,045], suggest that there is little or no significant involvement of supracrustal sources in the petrogenesis of the intrusion studied. Despite the strongly differentiated character of Azegour granitic rocks samples, their multi-element patterns shows many similarities to those of I-type granitoids, which has led to postulate that the parental liquids of A1-type were derived from partial melting of mafic magmas. The representative samples studied show less depleted εNd(t = 270 Ma)values of –0.94 to –4.85 and lower positive to slightly negative εSr(t = 270 Ma) values of –1.45 to 9.32. The isotopic data suggest that the Azegour granite was emplaced 270 myr ago, apparently generated by partial melting of a mafic/intermediate magma source in the lower crust as a result of the underplating of the asthenosphere mantle-derived Oceanic Island Basalt-like magmas. Alternatively, their isotopic signatures also can be attributed to the interaction and/or hybridisation of basaltic liquids derived from the mantle with these lower crust materials. The generated parental magma probably occurred at deep structural levels and involved fractional crystallisation processes by the separation of a mineralogical association composed of plagioclase + potassium feldspar ± biotite ± amphibole ± sphene ± apatite. The whole-rock Rb-Sr age of 268 ± 9 Ma, whole-rock geochemistry and Sr-Nd isotopic compositions of εNd(t = 270 Ma) and εSr(t = 270 Ma), combined with fieldwork data, suggest that the Azegour granite was emplaced.

Slab failure‐related magmatism in the Pinheiro Machado Complex, southern Dom Feliciano Belt, Brazil

In the Dom Feliciano Belt, Brazil, the Pinheiro Machado Complex (PMC) includes diorites, tonalites, granodiorites, syenogranites and granites, whose evolution is related to several magmatic pulses and complex petrogenetic processes. Two magmatic stages were identified (early and late), resulting in different rock subgroups. The geochemical data showed that the early magmatism was chemically affected by partial melting. Geochemical modelling results suggest that fractional crystallization processes with assimilation of around 40% from the crustal basement and the decoupling of assimilated magma are crucial for the PMC rocks' genesis. Geochemical data also show that during the early magmatism, the subsequent process of early diorite anatexis developed by heating and continuous activity of the underlying magma chamber possibly occurred at a melting rate of 5%–10%. The hybrid rocks have contributions from the mixing process related to early terms, showing geochemical correlations in the major element curves, for the early diorite and syenogranitic melt members, at 60%–50% and 50%–40%, respectively. Slab failure tectonic context is related to the multi‐intrusive events dynamics recorded in the studied rocks. Recharge and melting events of the recently formed crust due to the constant heating of new pulses of deep slab melting would explain the magmatic interactions observed in the Complex. The results demonstrate that the studied rocks crystallized in an open system, including mixing processes to form hybrid rocks, physical disaggregation and assimilation of early intrusions, truncation, dragging and erosion of early mushes by younger pulses.

Partial melting mechanisms of peraluminous felsic magmatism in a collisional orogen: An example from the Khondalite belt, North China craton

AbstractSedimentary‐derived (S‐type) granites are an important product of orogenic metamorphism, and a range of subtypes can be recognized by differences in field occurrence, mineralogy and geochemistry. These subtypes can reflect variations of initial protolith composition, partial melting reactions, pressure and temperature of anatexis, or magmatic processes that occur during ascent through the crust (e.g. mineral fractional crystallization or crustal assimilation). Together, these diverse factors complicate geological interpretation of the history of peraluminous felsic melt fractions in orogenic settings. To assess the influence of these factors, we performed integrated field investigation, petrology, geochemistry, geochronology and phase equilibrium modelling on a series of leucosomes within migmatite associated with different S‐type granites within the Khondalite belt, North China craton (NCC), which is an archetypal collisional orogen. Three types of leucosome are recognized in the east Khondalite belt: leucogranitic leucosome, K‐feldspar (Kfs)‐rich granitic leucosome and garnet (Grt)‐rich granitic leucosome. Phase equilibrium modelling of partial melting and fractional crystallization processes indicate that the leucogranitic leucosomes were mostly produced through fluid‐present melting, Kfs‐rich granitic leucosomes are produced through muscovite dehydration melting with 3 vol.% garnet fractional crystallization, and Grt‐rich granitic leucosomes are produced through biotite dehydration melting with 20–40 vol.% K‐feldspar fractional crystallization and up to 20 vol.% peritectic garnet entrainment. Mineral fractional crystallization and peritectic mineral entrainment occur in the source during melting, and play equally important roles in partial melting mechanisms in terms of affecting the geochemical compositions of granitic melts. Thus, we suggest that peraluminous felsic magmas preserved in collisional orogens are dominantly produced by fluid‐absent melting in the middle to deep continental crust, although extraction of low‐volume melt fractions from an anatectic source region at shallower depths during fluid‐present melting can also generate small amounts of S‐type granites that subsequently crystallize at high structural levels in the crust.

Experimental re-melting of a continental crust: probing the deep storage zone of Campi Flegrei and Vesuvius magmas

Mantle magmas interact with surrounding rocks during their ascent and storage in the continental crust, leading to open system processes as wall rock partial melting. In this study, we have experimentally investigated the reactions between a leucosome depleted migmatite and a primitive K-basaltic of Campi Flegrei (Italy). Experiments were carried out at pressure of 0.8 GPa temperatures from 1250 °C to 1050 °C and constant temperature and thermal gradient conditions. The experimental products consist of biotite-free migmatite, glass and crystals of clinopyroxene, olivine, plagioclase and Cr-spinel with proportions that vary as a function of temperature. Open system isothermal experiments indicate that the chemistry of melts and phase relationships are controlled by the high Al2O3 content of leucosome depleted migmatite with the glass composition shifting from K-trachybasalt towards shoshonite as the temperature decreases from 1200 °C to 1125 °C. At temperatures \\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\le$$\\end{document}1150°C, migmatite assimilation is not exclusively due to the assimilation fractional crystallization process because evidence of mingling and mixing is observed. T-gradient experiment shows melt composition ranging from shoshonite to phono-tephrite moving from the slightly crystalline zone (T = 1250 –1210 °C) at the bottom of the capsule towards the highly crystalline zone (T = 1160 –1140 °C). This SiO2-constant trend indicates that at temperature below the basalt solidus, the assimilation of leucosome depleted crust is represented almost exclusively by the biotite breakdown, leading to the increase in Al, Mg, Fe, Ti, and K activities in the system. The shoshonitic composition obtained in our experiments could represent the parental magma for both Campi Flegrei volcanic district and Vesuvius magmatic systems, indicating modification in a deep storage zone through mixing with the partial melts derived from restitic continental crust.

Stratigraphy, geochronology, geochemistry and Nd isotopes of the Ouarzazate Group, Anti-Atlas, Morocco: Evidence of a Late Neoproterozoic LIP in the northwestern part of the West African Craton

In the eastern and central Anti-Atlas of Morocco, the Late Neoproterozoic Ouarzazate Group (OG) forms a ∼ 2 km-thick section of volcano-sedimentary rocks deposited during intermittent magmatic activity, spanning a time period between 590 and 540 Ma. In the eastern Anti-Atlas, the stratigraphy of the OG, termed IMS (Imiter Mine succession), includes four units that reflect a gradual change from fluvial to lacustrine depositional sedimentary environments. In the central Anti-Atlas, the deposition of the OG occurs within a caldera environment, consisting of five units referred to as BMS (Bou Azzer Mine succession). UPb dating on zircon from the rhyolite lava flow at the top of the IMS constrains the latest lava flow of the IMS to 570.7 ± 2.1 Ma. In the Bou Azzer inlier, the stratigraphically correlated basal andesite and top dacite lava flows were emplaced at 590.6 ± 4.2 Ma and 555.9 ± 20.4 Ma, respectively, suggesting that the OG was constructed through successive pulses within a long-lived magmatic episode. The magmatic rocks display geochemical signatures typical of continental arc magmas, including high-K calc-alkaline to shoshonite composition, enrichment in LILE, and negative Nb, Sr, Ti and P anomalies. Nd isotopes indicate that magmas supplying the plumbing systems of the IMS and BMS constitute transitional products resulting from a combination of orogenic and intraplate volcanism, involving deep crustal recycling. The compositions of these magmas evolved through processes of crustal contamination, bulk assimilation, and minor fractional crystallization of the parent melt. High εNd values of the BMS rocks argue for a juvenile origin, whereas lower εNdt recorded in the IMS likely reflect old crustal protoliths and an overall less contribution of juvenile material in their source. The magmatic rocks of the OG are interpreted as products of a large igneous province (LIP) developed by a post-collisional delamination model that initiated tens of millions of years after the subduction-collision process stage of the Pan-African orogeny in the northwestern part of the West African Craton (WAC).

Mechanism of beryllium mineralization in a granite-pegmatite system: Constraints from ore geology and beryl mineralogy of the large Arskartor Be-Nb-Mo deposit, southern Chinese Altai

The Arskartor Be-Nb-Mo deposit is the second largest Be deposit in the Chinese Altai, NW China, which hosts over 11,000 tons of BeO resource. The muscovite-albite granite and rare-metal pegmatite in the ore district are spatially and temporally coexisted and both are beryllium mineralized. The muscovite-albite granitic stock can be divided into a barren zone and a Be-mineralized zone. The pegmatite shows an well-developed internal zone including the layered muscovite-quartz-albite zone, (lower) beryl-muscovite-quartz zone, quartz core, (hanging) beryl-muscovite-quartz zone, and muscovite-quartz-microcline zone. Beryl is the dominant Be-bearing mineral and mainly occurs in the Be-mineralized granite, the layered muscovite-quartz-albite and the beryl-muscovite-quartz zones of the pegmatite. Subhedral to euhedral beryl in the Be-mineralized granite is interstitial to or intergrown with rock-forming minerals. In contrast, beryl crystals in the pegmatite are coarser in grain size and more euhedral in shape, and mainly coexist with coarse “booked” muscovite and blocky quartz. Concentrations of Li, Cs and Na/Li ratios of beryl are 184–760 ppm, 218–1996 ppm, and 2.13–21.3, respectively. The progressive variations of incompatible elements compositions and Na/Li ratios are consistent with the fractional crystallization mechanism of the granite-pegmatite system. Paragenesis and internal structure of beryl suggest nonequilibrium crystallization of a relatively incompatible elements and fluxes-enriched late granitic melt, generated the coarse-grained Be-mineralized granite. With the progressive enrichment of incompatible and fluxing elements and decreasing temperature, liquidus overcooling was achieved and generated the aplite and immediate zoned pegmatite that hosts abundant beryl. Moreover, the differentiating pegmatitic melt with varying amounts of aqueous fluids at different melt fractions, likely resulted in heterogeneous distribution of beryllium and subsequent variable amounts of beryl crystallization in different internal zones. The exsolution of aqueous fluids from the residual pegmatitic melt resulted in Mo-mineralization and related hydrothermal alteration. Consequently, both protracted fractional crystallization and subsolidus processes contributed the formation of the Arskartor granite-pegmatite system with Be-polymetallic mineralization.

Geochemical fingerprinting of continental crust trapped in Cadomian volcanic arcs along northern Gondwana

During the Ediacaran to Cambrian periods, the extensive Avalonian–Cadomian accretionary orogen formed along the northern margin of the Gondwana (Pannotia) supercontinent. One of the best-preserved magmatic arcs within this orogenic system is the Davle volcanic complex (DVC) in the Teplá–Barrandian unit of the Bohemian Massif. Using detailed field observations, petrography, major/trace element concentrations, Nd–Hf isotopic compositions as well as U–Pb zircon dating, we interpret a complex evolutionary history of the DVC as comprising three main stages. The first stage (∼610–570 Ma) is represented by a volcano-plutonic association of andesite, dacite, rhyolite and tonalite–trondhjemite–granodiorite (metamorphosed to orthogneiss). A wide range of major/trace element contents together with highly variable εNd values (+3.6 to –5.1) suggest derivation from a juvenile (mantle-derived) source with subsequent assimilation of cratonic crust during magma emplacement, also supported by the modelling of the assimilation–fractional crystallization (AFC) process. The second stage (∼580–560 Ma) is characterized by a gradual termination of the volcanic arc activity, followed by a deposition of marine siliciclastic succession comprising, from the bottom to the top, laminated tuffs, silicified black shales (Lečice Member), and a thick turbidite greywacke–shale–conglomerate sequence (Štěchovice Group). The third stage of poorly constrained age (∼570–500 Ma) is represented by an intra-arc extension and intrusion of juvenile trondhjemite and related rhyolite dykes (εNd +4.8 to +8.4). Finally, we compare these findings with zircon U–Pb ages and whole-rock Nd isotopic data from other Cadomian terranes and propose that the cratonic crust played an important role in recycling along the whole orogenic belt. Thus, we conclude that the Cadomian Orogen formed as a collage of fringing (such as modern Japan, Taiwan, or Philippines) and continental (as modern Andes) arcs of variable evolutionary stages rather than as a belt dominated by intra-oceanic island arcs.

High-pressure minerals and new lunar mineral changesite-(Y) in Chang’e-5 regolith

Forty-five years after the Apollo and Luna missions, China’s Chang’e-5 (CE-5) mission collected ∼1.73 kg of new lunar materials from one of the youngest basalt units on the Moon. The CE-5 lunar samples provide opportunities to address some key scientific questions related to the Moon, including the discovery of high-pressure silica polymorphs (seifertite and stishovite) and a new lunar mineral, changesite-(Y). Seifertite was found to be coexist with stishovite in a silica fragment from CE-5 lunar regolith. This is the first confirmed seifertite in returned lunar samples. Seifertite has two space group symmetries (Pnc2 and Pbcn) and formed from an α-cristobalite-like phase during “cold” compression during a shock event. The aftershock heating process changes some seifertite to stishovite. Thus, this silica fragment records different stages of an impact process, and the peak shock pressure is estimated to be ∼11 to 40 GPa, which is much lower than the pressure condition for coexistence of seifertite and stishovite on the phase diagram. Changesite-(Y), with ideal formula (Ca8Y)□Fe2+(PO4)7 (where □ denotes a vacancy) is the first new lunar mineral to be discovered in CE-5 regolith samples. This newly identified phosphate mineral is in the form of columnar crystals and was found in CE-5 basalt fragments. It contains high concentrations of Y and rare earth elements (REE), reaching up to ∼14 wt. % (Y,REE)2O3. The occurrence of changesite-(Y) marks the late-stage fractional crystallization processes of CE-5 basalts combined with silicate liquid immiscibility. These new findings demonstrate the significance of studies on high-pressure minerals in lunar materials and the special nature of lunar magmatic evolution.

Sr- and Nd-Isotope Geochemical Effects of Assimilation and Fractional Crystallization (AFC) Processes in the Heterogeneous Crust: The Example of Ferrobasites from the Ladoga Graben (Karelia, Russia)

Sr- and Nd-Isotope Geochemical Effects of Assimilation and Fractional Crystallization (AFC) Processes in the Heterogeneous Crust: The Example of Ferrobasites from the Ladoga Graben (Karelia, Russia)

Mineral chemistry and thermobarometry of Jurassic arc granitoids: implications for petrotectonic and unroofing history of the southern Colombian Andes

Abstract The Jurassic magmatic record in the southern Colombian (Northern Andes) includes numerous subduction-related I-type calc-alkaline granitoids with diverse structures and textures, formed in two main episodes at ∼195 to 165 Ma and ∼165 to 145 Ma. We provide new insights into the mineral chemistry, estimates of intensive parameters and petrogenetic processes of 12 plutonic occurrences in the region, grouped in 4 petrographic associations. Primary mineral assemblages include labradorite-to-oligoclase, alkali feldspars, ferroan enstatite, Mg-rich augite to ferroan-diopside, tschermakite to hastingsite and hornblende and Mg-rich annite; Fe-rich phlogopite and actinolite are post-magmatic phases. Amphibole chemistry indicates that the older (195–165 Ma) Jurassic bodies formed from relatively highly oxidized (fO2 values buffered at −0.1 ≤ NNO ≤ +1.4) hydrous (∼4 to 6 wt % H2O) magmas and their differentiation involves significant crustal assimilation and/or magma mixing, fractional crystallization and late-magmatic re-equilibration processes. In contrast, the younger (165–145 Ma) Jurassic intrusives, derived from subducted-modified mantle sources, record moderately lower oxidized hydrous conditions (fO2 values −0.7 to 0.8 ≤ NNO; ∼5 wt % H2O) with magma evolution mainly controlled by fractional crystallization and late-magmatic re-equilibration processes. Clinopyroxene-only, amphibole-only and amphibole-plagioclase thermobarometry estimations suggest that the Jurassic occurrences crystallized over variable temperature (647°C–1087°C) and pressure (0.7–6.3 kbar) conditions, corresponding to emplacement depths ranging from ∼15, ∼8 to 11, ∼5 to 7 and &lt;4 km along the arc crustal column. The obtained data combined with time evolution allow the identification of exhumed and fragmented arc blocks in the Jurassic magmatic system and provide an essential link between the orogenic deformation event poorly constrained in the Northern Andes.