Crystallization Sequence Of Minerals Research Articles

Amphibole geochemistry in the Haobugao skarn Zn-Fe-Sn deposit in the southern Great Xing’an Range: Implications for the ore-forming process

The Haobugao Zn-Fe-Sn deposit is a typical skarn deposit in the southern Great Xing’an Range of NE China. Despite many advances in understanding its genesis, the detailed ore-forming processes of Zn, Fe and Sn are still unclear. Amphibole, a rock-forming mineral, has been well studied as an indicator of diverse magmatic and metamorphic processes; however, the geochemistry of hydrothermal amphibole has previously received less attention. The Haobugao deposit contains two generations of hydrothermal amphibole (Amp-I and Amp-Ⅱ), which provides a good opportunity to use amphibole geochemistry to trace the mineralization process. Early Amp-I coexists with cassiterite, magnetite and quartz, whereas late Amp-II coexists with quartz and sulfides and can be further divided into two subgroups: Amp-Ⅱa (in skarn) and Amp-Ⅱb (in the country rocks of siltstone). The oxygen isotopic compositions of the fluid (δ18Ofluid 2.9‰) responsible for the Amp-I formation indicate that the amphiboles formed from mixed magmatic fluid with meteoric water. Amp-I is LREE-depleted and HREE-enriched with obvious negative Eu anomalies. Amp-Ⅱ is generally slightly LREE-depleted with negative or positive Eu anomalies and positive Ce anomalies. The incorporation of trace and rare elements is mainly controlled by the fluid composition. Detailed petrological observations and amphibole geochemistry, combined with previous research results, confirm that Sn, Fe, Pb and Zn mineralization occurred during a single mineralization event. From the oxide to the quartz sulfide stage, the ore-forming fluid evolved from high-temperature and oxidized conditions with enrichment of Sn, Li, Be and REEs to low-temperature and reduced or oxidized conditions with enrichment of Cu, Co and Zn. The concentrations of Cu, Co and Zn in different amphiboles vary with the mineral crystallization sequence. This study shows that amphibole geochemistry can be useful for tracing fluid evolution and mineralization processes in hydrothermal systems.

Diverse apatite geochemical compositions in early Paleozoic granitoids of the North Qinling orogen, China: Insights into their petrogenesis and magma sources

Apatite geochemistry in granitoids is controlled primarily by the original melt compositions and partition coefficients. However, additional factors (e.g., post-crystallization effects, mineral crystallization sequences, and crustal assimilation) can also contribute to variations in apatite compositions. In this study, we collected three groups of early Paleozoic granitoids from the North Qinling Orogen and obtained in situ geochemical data for apatite. The granitoids were formed by partial melting of oceanic arc crust (group A), recycling of ancient crust (group B), and melting of the lithospheric mantle and extensive fractionation (group C). Trace element and Nd isotope data show the apatite from the Taiping and Manziying plutons (group A) were affected by post-crystallization processes and crustal assimilation, respectively. In addition, crystallization of plagioclase/allanite and apatite resulted in the variable Eu anomalies and rare earth element contents of apatite in the group A granitoids. In contrast, apatite compositions in group C were controlled primarily by the fractionation of hornblende. However, the decoupling of Eu anomalies of apatite and their host rocks, particularly for group B, cannot be easily explained by the aforementioned factors. As such, the redox state may also have been an important factor. We used a ternary diagram (10 × [Eu/Eu*]N–V–Ga) to constrain the redox state from the apatite data, and provide insights into the types and petrogenesis of the host granitoids. Combined with the whole-rock and zircon geochemical data, we found that the apatite from the rocks derived from continental crust (group B and cratonic adakites) is generally reduced, whereas apatite from the mafic rocks and high BaSr granitoids is highly oxidized. The highest degree of oxidation was found for the altered apatite from the group A granitoids and unaltered apatite in the orogenic adakites, possibly due to interactions with fluid derived from oceanic crust. Moreover, unaltered group A granitoids exhibit a transitional trend from an oxidized to a reduced state. Apatite geochemistry can be used to constrain the redox state of adakitic rocks and whether they have a continental or oceanic crustal origin. The high Sr contents of high BaSr granitoids are inherited from their mantle source.

Geochemistry of Rocks at the Neskevara Rare-Metal Deposit of the Vuoriyarvi Alkaline–Ultramafic Complex, Kola Peninsula

The Vuoriyarvi Paleozoic alkaline–ultramafic complex with carbonatites is made up of a great diversity of rocks with various ore mineralization. The paper presents data on the geochemistry of pyroxenites, phoscorites, and carbonatites from the Neskevara deposit of rare metals. The pyroxenites of the rare-metal deposit are significantly enriched in Nb, Ta, and Th relative to the primitive mantle and the primary alkaline–ultramafic melt composition calculated for the Kola alkaline province and are characterized by high Nb/Ta, Zr/Hf, and Th/U ratios of 29, 35, and 14, respectively. HFSE are maximally enriched in the phoscorites and carbonatites of stages II and III, with the highest concentrations of Nb (16 000 ppm), Th (2800 ppm), and Zr (4000 ppm) found in the calcite–tetraferriphlogopite phoscorites, in which pyrochlore crystallization on the liquidus was identified. The rocks of the carbonatite series are strongly enriched in LREE relative to carbonaceous chondrite. The calcite–dolomite carbonatites of the late magmatic–carbothermal stage show REE enrichment up to 25 800 ppm. The chondrite-normalized REE patterns and (La/Yb)N ratio indicate that REE were systematically more strongly fractionated in the sequence pyroxenite (70)—phoscorite (90)—calcite (540) and dolomite (3790) carbonatites The crystallization sequence of minerals in the rare-metal phoscorites and carbonatites of intermediate stages indicates that magnetite and pyrochlore crystallized nearly simultaneously. The crystallization temperatures of such associations are, according to data of the magnetite–ilmenite thermometer, lower than 500–600°C, at ∆NNO = –0.3 and + 1.5 and corresponded to the temperature at which the rare-metal ore mineralization of the main stage was formed.

In Situ Mineralogical Constraints on Magmatic Process for Porphyry Deposits in the Upper Crust: A Case from Tongchang–Chang’anchong Porphyry Deposits, SW China

The magmatic process within upper crust encompasses various contents such as the transition between magmatic and hydrothermal systems and changes in oxygen fugacity (ƒO2), which ultimately play key roles in the formation of porphyry Cu deposits (PCDs). However, tracing these magmatic processes, especially in porphyry systems, is not an easy task. This study reported the detailed process of magmatic fluid exsolution and systematical variation of magmatic ƒO2 within the upper crust of a Tongchang–Chang’anchong porphyry Cu deposit, based on detailed investigations of mineral crystallization sequences and compositional features of the minerals in the fertile porphyries. Results indicate that the fertile porphyries show a high initial ƒO2, with ΔFMQ ≥ +3.0 (ΔFMQ is the deviation of logƒO2 from the fayalite–magnetite–quartz (FMQ) buffer). The magmatic ƒO2 (ΔFMQ) continued to decrease to ~+2 until fluid exsolution occurred at ~790 °C due to wall-rock contamination. The magmatic fluid exsolution process caused a temporary increase in the ƒO2 (to ΔFMQ = ~+3.4). The high magmatic ƒO2 during this process (790–750 °C) resulted in a higher content of ore-forming materials in the exsolved magmatic fluid. When the temperature dropped below 750 °C, the magmatic ƒO2 began to continuously decrease and eventually reached ΔFMQ = ~+0.6. The lower magmatic ƒO2 hindered the further migration of ore-forming materials through the exsolved fluid during this process (< 750 °C). Results of this study indicate that the initial magma during the upper crustal magmatic process of PCDs generally has a high ƒO2, and the contamination of reduced components can significantly decrease the magmatic ƒO2. The early magmatic fluid exsolution process can maintain a high magmatic ƒO2 condition, thereby efficiently extracting ore-forming minerals and producing ore-forming fluids, which is the key to the formation of PCDs. The latter continuous decrease in magmatic ƒO2 during the fluid exsolution process may be the reason preventing the Tongchang–Chang’anchong porphyry Cu deposit to form a giant PCD.

Apatite and Zircon Geochemistry in Yao’an Alkali-Rich Porphyry Gold Deposit, Southwest China: Implications for Petrogenesis and Mineralization

The Yao’an gold deposit is located in the middle of the Jinshajiang-Ailaoshan alkali-rich metallogenic belt, and this belt hosts many porphyry-type Cu-Au-Mo deposits formed at 46–33 Ma. Yao’an porphyry gold-mineralization is intimately associated with biotite syenite porphyry, whereas the contemporaneous quartz syenite porphyry is barren. In this study, we compared the major and trace elements of apatite and zircon and isotopic compositions of zircon from the biotite syenite porphyry and quartz syenite porphyry, to explore their geochemical differences that may affect their mineralization potential. The results show that both porphyries were derived from the partial melting of the thickened lower crust, which has been modified by slab-derived fluids, but has different mineral crystallization sequences, magma fluid activities, and magma oxidation states, respectively. REE contents in apatite and zircon can be used to reveal the crystallization sequence of minerals. A rapid decrease of (La/Yb)N ratio in apatite from both porphyries may be caused by the crystallization of allanite. Large variation of Cl contents and negative correlation between F/Cl and (La/Yb)N in apatite from fertile porphyry indicate that it has experienced the exsolution of Cl-bearing hydrothermal fluid. Higher Y/Ho and lower Zr/Hf in zircon from fertile porphyry indicate a stronger fluid activity than barren porphyry. The high S, V, As contents, δEu, low δCe in apatite, as well as high Ce4+/Ce3+ and log(fO2) estimated from zircon geochemistry from fertile porphyry, indicate high a oxidation state of fertile porphyry, similar to other fertile porphyries in this metallogenic belt. High fluid activity and fluid exsolution are conducive to the migration and enrichment of metal elements, which are very important for mineralization. High oxygen fugacity inhibits the precipitation of metal in the form of sulfide, thereby enhancing the mineralization potential of rock. Therefore, the exsolution of Cl-bearing hydrothermal fluid and high oxygen fugacity are the key factors promoting mineralization in Yao’an area.

Iron isotope fractionation in reduced hydrothermal gold deposits: A case study of the Wulong gold deposit, Liaodong Peninsula, East China

Abstract Iron isotope fractionation in hydrothermal systems is a useful diagnostic tool for tracing ore-forming processes. Here, we report on the Fe isotopic compositions of a suite of hydrothermal minerals from ores (pyrite, pyrrhotite, and quartz) from the Wulong gold deposit, Liaodong Peninsula, East China. Pyrites from quartz sulfide ores show a δ56Fe (56Fe/54Fe in the sample relative to IRMM-14) range from +0.11 ± 0.03‰ to +0.78 ± 0.03‰ (2SD), and pyrrhotites from the same vein are isotopically lighter than the pyrites, varying between −0.85 ± 0.01‰ and −0.07 ± 0.00‰. This result is consistent with theoretical predictions of equilibrium fractionation and published mineral compositions. For the first time, to our knowledge, we report the Fe isotopes of hydrothermal quartz that records the isotopic compositions of the ore-forming fluids. Two quartz separates in the quartz-sulfide vein yield δ56Fe values of −0.02 ± 0.02‰ and +0.07 ± 0.07‰. Our Fe isotope fractionation calculations show that pyrrhotite with light Fe isotopes crystallized first from the ore-forming fluids, which indicates a relatively reduced condition for the initial ore-forming fluids. Then the remaining fluids with heavy Fe isotopes precipitated pyrites with positive δ56Fe values, and their mineral crystallization sequence records an increase of oxygen fugacity during mineralization. Gold deposits in Wulong and Jiaodong share many similar geological characteristics. The pyrites from the Wulong deposit have higher δ34S values (+0.5 to +4.1‰) than the pyrrhotites (–1.2 to +1.2‰). Pyrites from the Jiaodong gold deposits show a wide range of both positive and negative δ56Fe values as well as high δ34S values, whereas those from the Wulong deposit have a relatively narrow range of positive δ56Fe values and near-zero δ34S values. The differences in Fe isotopes may be due to early precipitation of pyrrhotite with light Fe isotopes under a relatively low oxygen fugacity environment in the Wulong deposit, resulting in pyrite precipitated from the remaining fluids with heavy isotopes. The sulfur isotope variations between Wulong and Jiaodong gold deposits reflect differences in their source regions rather than oxygen fugacities. In addition, we have compiled Fe isotopic compositions of pyrites and pyrrhotites from different types of ore deposits to investigate their Fe isotopic behavior in magmatic-hydrothermal systems. Pyrite grains show a wide range of δ56Fe values. Positive pyrite δ 56Fe values reflect an equilibrium isotope effect, whereas negative pyrite δ56Fe values may be due to kinetic isotope effects or to a mixture of sedimentary host rocks. Pyrrhotite grains show similar negative δ56Fe values, and they have a strong influence on the Fe isotope systematics in magmatic and hydrothermal systems. Our data show that Fe isotopes can be used to trace precipitation orders of pyrite and pyrrhotite and oxygen fugacity evolution in relatively reduced hydrothermal deposits.

Mineralogical and Geochemical Study on the Yaojiazhuang Ultrapotassic Complex, North China Craton: Constraints on the Magmatic Differentiation Processes and Genesis of Apatite Ores

The differentiation process of ultrapotassic magmas is enigmatic and poorly understood. The Yaojiazhuang ultrapotassic complex is concentrically zoned by late-intruded syenite in the core and early emplaced clinopyroxenite in the periphery, combining a “bi-modal” lithology. Spatially, apatite and iron oxide-apatite (IOA) ores, glimmerite and pseudoleucite occur in the upper part of clinopyroxenite. The syenite and clinopyroxenite are composed of variable amounts of clinopyroxenite, biotite, K-feldspar, magnetite, apatite with minor analcite, titanite and primary calcite. The pseudoleucite clinopyroxenite contains mainly clinopyroxene, biotite and garnet in the matrix, and nepheline–K-feldspar intergrowth with muscovite and minor celestine in the leucite pseudomorph. Geochemically, rocks of the Yaojiazhuang complex are significantly enriched in potassium (K), light rare earth elements (LREE) and large ion lithophile elements (LILE). Crustal contamination by Archean tonalite–trondhjemite–granodiorite (TTG) gneisses basement may play an important role to convert the syenitic melts from silica-undersaturation to saturation. Fractionation crystallization is supported by the mineral crystallization sequence to explain the bimodal lithologies instead of silicate liquid immiscibility. During the magmatic evolution, decompression, fractionation of volatile-poor clinopyroxene and the enhancement by CO2 may result in the exsolution of an aqueous fluid. The late-stage interactions between existing minerals and magmatic fluids in the crystal mush could be a key process in the generation of both leucite pseudomorphs and apatite/IOA ores.

Discrepancy between bulk-rock and zircon Hf isotopes accompanying Nd-Hf isotope decoupling

Abstract Zircon is an important accessory mineral for studying the crust-mantle interaction and crustal growth through time because zircon crystals not only allow precise dating but also record initial Hf isotope ratios of the host magma. Our study on a suite of gabbronorite, mafic diorite cumulate, diorite and granite from the Kekeli Batholith in the North Qilian Orogenic Belt, Northern Tibetan Plateau, shows (1) a significant Hf isotope discrepancy between zircon and their bulk rocks; and (2) bulk-rock Nd-Hf isotope decoupling. These observations thus demonstrate that zircons do not always capture the full history of magmatic system. The significant positive correlation between bulk-rock Hf isotope ratios and TiO2 content (R2 = 0.94) indicates that Ti-rich minerals (e.g., ilmenite, amphibole) are likely important Hf hosts. The early-formed Ti-rich minerals possibly record different Hf isotopes from those of zircons crystallized subsequently, thus causing discrepancy between zircon and bulk-rocks and leading to bulk-rock Nd-Hf isotope decoupling. Correlations between bulk-rock TiO2 content, Mg isotopes and Hf isotopes indicate a mixing process, with granite and gabbronorite representing two compositional endmembers. Because Ti minerals have higher crystallization temperatures than zircons, when the mixing melts have contrasting isotopes (or from heterogeneous sources/have a strong crustal contamination), the bulk-rock and zircon Hf isotope discrepancies reflect mineral crystallization sequence during mafic and felsic magma mixing. It is thus imperative to consider early formed minerals such as Ti-rich minerals and the bulk rock composition, not just zircons, when using Hf isotopes to track melt evolution and precisely constrain mantle contribution to granitoid petrogenesis.

Redox-controlled generation of the giant porphyry Cu–Au deposit at Pulang, southwest China

Some porphyry Cu–Au deposits with relatively reduced ore assemblages, characterized by high hydrothermal pyrrhotite contents and a lack of primary hematite and magnetite, are generally considered to be associated with reduced I-type granitoids. However, the role of magmatic oxygen fugacity (fO2) in controlling Cu–Au mineralization in such reduced porphyry deposits is poorly understood. The giant Late Triassic (ca 216 Ma) Pulang porphyry Cu–Au deposit of southwest China shows typical reduced ore assemblages. This study reported the systematical variation of upper crustal magmatic fO2 of Pulang deposit, based on detailed investigations of mineral crystallization sequences and compositional features of the mineralization-related porphyries (early P1 and late P2 porphyry). Results indicate that magma of the mineralization-related porphyries experienced complex fO2 fluctuations during its upper crustal evolution. The early primary magma had very high initial fO2, with ΔFMQ ≥ + 3.0 at depths of > 12 km [ΔFMQ is the deviation of logfO2 from the fayalite–magnetite–quartz (FMQ) buffer]. The fO2 of evolved parental magma subsequently decreased, with ΔFMQ ≤ + 1.9, due to injection of relatively reduced dioritic magmas (ΔFMQ = + 1.4 to + 2.3) from a deeper chamber (17–21 km depth) into the primary magma chamber at 10–12 km depth. Magma mixing had largely ceased at 6–10 km depth. The parental magma then ponded within the reduced Tumugou formation at a depth of ~ 3.7 km where magmatic fO2 decreased to a moderately oxidized state (ΔFMQ = ~ + 1.6), and finally to a moderately reduced state [reflected by log(Fe2O3/FeO) ratios of − 0.5 for P2 porphyry]. Results of this study of magmatic fO2 indicate that porphyry magmas associated with reduced Pulang ore assemblages were initially generated as highly oxidized magma which was subsequently reduced through magma mixing and contamination by reduced sedimentary rocks of the Tumugou Formation. The sharp fO2 decrease at very shallow depth prevented the early loss of Cu and Au because the magma remained oxidized until it was emplaced at ~ 3.7 km depth. Moderately reduced magmas may thus have a genetic association with porphyry Cu–Au mineralization.

Mineral Phase Crystallization Sequence of Delta Steel Company (DSC), Ovwian-Aladja, Western Niger Delta Steelmaking Slag for Use as Material in Industry

Slag is a non-metallic by-product obtained in the refining of metals from metallic ores. Slag production at the Delta Steel Company (DSC), Ovwian-Aladja, western Niger Delta, follows the direct iron reduction steelmaking process. Fifteen company slag samples collected were examined by x-ray fluorescence, thin section petrography and electron microprobe analyses to establish the mineralogy and mineral crystallization sequence and thus explain their occurrences. The results show the presence of synthesized silicate minerals of belite, melilite and merwinite; calcium aluminate, wustite, periclase, perovskite and glass in the slag formed at between the temperatures of 1500°C and 500°C. Crystallization sequence is alpha (α) form of belite (1500°C-1420°C), alpha high (α/H) belite (1420°C-1160°C), alpha low (α/L) belite (1160°C-680°C, beta (β-) belite (680°C – 630°C), Melilite (1420°C-680°C), aluminate, merwinite, wustite, periclase, peruvskite and glass (630°C–500°C) in that order. This study has revealed that in behavior, synthetic minerals also crystallize from high to low temperature forms as is the case with natural minerals formed from silicate magmas. The forming behaviour of these minerals confers on them the important characteristics for industrial use as an industrial mineral compliment to natural materials.

Mineralogical characteristics of polymetallic sulfides from the Deyin-1 hydrothermal field near 15°S, southern Mid-Atlantic Ridge

A seafloor hydrothermal field, named Deyin-1 later, near 15°S southern Mid-Atlantic Ridge (SMAR) was newly found during the 22nd cruise carried out by the China Ocean Mineral Resources Research & Development Association (COMRA). Sulfide samples were collected at three stations from the hydrothermal field during the 26th cruise in 2012. In this paper, mineralogical characteristics of the sulfides were analyzed with optical microscope, X-ray diffractometer, scanning electron microscope and electron microprobe to study the crystallization sequence of minerals and the process of hydrothermal mineralization. According to the difference of the ore-forming metal elements, the sulfide samples can be divided into three types: (1) the Ferich sulfide, which contains mainly pyrite and chalcopyrite; (2) the Fe-Cu-rich sulfide consisting predominantly of pyrite, chalcopyrite and isocubanite, with lesser amount of sphalerite, marmatite and pyrrhotine; and (3) the Fe-Zn-rich sulfide dominated by pyrite, sphalerite and marmatite, with variable amounts of chalcopyrite, isocubanite, pyrrhotine, marcasite, galena and gratonite. Mineral precipitations in these sulfides are in the sequence of chalcopyrite (isocubanite and possible coarse pyrite), fine pyrite, sphalerite (marmatite), galena, gratonite and then the minerals out of the dissolution. Two morphologically distinct generations (Py-I and Py-II) of pyrite are identified in each of the samples; inclusions of marmatite tend to exist in the coarse pyrite crystals (Py-I). Sphalerite in the Fe-Zn-rich sulfide is characterized by a “chalcopyrite disease” phenomenon. Mineral paragenetic relationships and a wide range of chemical compositions suggest that the environment of hydrothermal mineralization was largely changing. By comparison, the Fe-rich sulfide was formed in a relatively stable environment with a high temperature, but the conditions for the formation of the Fe-Cu-rich sulfide were variable. The Fe-Zn-rich sulfide was precipitated during the hydrothermal venting at relatively low temperature.

Amphibolite facies retrograde metamorphism of the Zhujiachong eclogite, SE Dabieshan: 40Ar/39Ar age constraints from argon extraction using UV‐laser microprobe, in vacuo crushing and stepwise heating

AbstractThe Zhujiachong eclogite in the south‐eastern Dabieshan ultra‐high‐P terrane has been overprinted during retrograde metamorphism, with the development of garnet‐amphibolite mineral assemblages in most rocks in the outcrop. This study is focused on providing age constraints for the retrograde amphibolite facies and greenschist facies mineralogy by 40Ar/39Ar dating. By applying a novel approach of combining three different techniques for extracting argon: laser stepwise heating of single grains and small separates, a spot fusion technique by UV‐laser ablation microprobe on polished sections and an in vacuo crushing technique for liberating radiogenic argon from fluid inclusions, it is demonstrated that an internally consistent thermal history can be derived. The 40Ar/39Ar ages indicate that phengite formed before 265 Ma, probably during the ultra‐high‐P event. Ages associated with amphibolite facies retrograde metamorphism range from 242 to 217 Ma by the analyses of amphibole. Ages of c. 230 Ma were found for the symplectite matrix that formed during retrogression from eclogite pyroxene. Late stage hydrothermal activity leading to the formation of coarse‐grained paragonite and fluid inclusions in vein amphibole was dated at c. 200 Ma. These age results agree well with the mineral crystallization sequence observed from thin‐sections of the retrograded eclogite: phengite → paragonite and amphibole in matrix → amphibole in the corona.

The Dongcaohe ophiolite from the North Qilian Mountains: A fossil oceanic crust of the Paleo-Qilian ocean

The Dongcaohe ophiolite, located at the south of the North Qilian subduction complexes, is a tectonic block with an exposed area of about 3 km×6 km. It consists of an intrusive section overlain by an extrusive section. The lower part of the intrusive section consists of cyclic layers of cumulate dunites, troctolites, anorthosites, anorthositic gabbros, and gabbros with small discordant dunite and troctolite bodies. This layered sequence grades upward to isotropic gabbros and gabbronorites, which are overlain by the extrusive sequence of diabasic sheeted dikes and basaltic lavas. The overall mineral crystallization sequence was olivine±Cr-spinel, plagioclase, clinopyroxene, orthopyroxene, and Fe-Ti oxides. The Cr-spinel (Mg#: 42–66, Cr#: 41–57) in these layered cumulates and present-day abyssal peridotites have similar compositions. Also, the compositional variations of the plagioclase and clinopyroxene in the intrusive section reflect crystallization from melts compositionally similar to the present-day ocean basalts. Moreover, the rare earth element (REE) and multi-element distribution patterns of the intrusive and extrusive lithologies in the Dongcaohe ophiolite are consistent with crystallization of mid-ocean ridge basalts. The zircon grains separated from the gabbronorite have an SHRIMP average 206Pb/238U weighted age of 497 ± 7 Ma, which is considered as the tectonic emplacement age of the Dongcaohe ophiolite. The field occurrence, mineral and whole-rock compositions indicate that the Dongcaohe ophiolite represents a well-persevered oceanic crustal fragment composed of a complete oceanic crustal section of layered cumulates at bottom upgrading through isotropic cumulates to sheeted dikes and lava flows.

The Origin of Marginal Compositional Reversals in Basic-Ultrabasic Sills and Layered Intrusions by Soret Fractionation

Marginal reversals—a common feature of many basic differentiated igneous bodies regardless of their size and bulk composition—are remarkable in being a mirror of the Layered Series. These are distinguished by: (1) an apparent lack of mass balance between the lower part of the marginal reversals, including chilled margins, and the bulk composition of the intrusions; (2) mineral crystallization sequences and (3) mineral compositional trends, which are both essentially the opposite of those in the Layered Series; (4) the cotectic composition of rocks composing the marginal reversals; (5) the capacity to form from both phenocryst-rich and phenocryst-free parental magmas; (6) the capability to develop along the floor, subvertical walls and even the roof of magma chambers. None of the current models of magma chamber evolution can provide an adequate explanation for the characteristic features of the marginal reversals. The problem can be resolved in the context of a model combining Soret diffusion in thin liquid boundary layers at the magma chamber margins and vigorous convection in the main magma body. The key proposal is that the formation of marginal reversals takes place through the non-equilibrium evolution of liquid boundary layers as a result of a temperature gradient imposed by the cold country rock. The fundamental explanation for the mirror image of a marginal reversal is that the non-equilibrium Soret fractionation works in a manner opposite to that of the equilibrium crystal–liquid fractionation that produces the Layered Series.

Magma evolution observed in the Matsuura basalts in northwest Kyushu, Japan: An example of high-pressure open system fractional crystallization in a refilled magma chamber near the crust–mantle boundary

Formation of an extensive shallow water sedimentary basin before the voluminous Matsuura basalt volcanism in the back arc volcanic belt in northwest Kyushu, Japan, seems to indicate the lower crust erosion due to the upwelling of the mantle, which results in the decompression melting of mantle to form basaltic magma. The Matsuura basalts, 10 to 1 Ma, range in composition from low alkali tholeiitic basalt through alkali olivine basalt to basaltic andesite. Their compositions show a wide variation in MgO from 11.6 wt.% to 2.8 wt.%. Their chemical characteristics are: (1) evolution across the alkali–subalkali boundary, (2) crescent form of the basalt distribution on a SiO 2 vs. MgO diagram, (3) enrichment in normative plagioclase component and a diminution in normative clinopyroxene component with the magma evolution, (4) abrupt termination of this plagioclase-enrichment trend at MgO=3.3 wt.%, (5) marked enrichment in SiO 2 in aphyric basalts with MgO<5.5 wt.%, (6) a limit of magma evolution, and (7) magma mixing. Mineral crystallization sequence is found to be olivine, olivine+clinopyroxene, and then olivine+clinopyroxene+plagioclase. Iron oxide crystallization starts in iron-enriched magmas a little before the joining of plagioclase in crystallization, which results in the rapid enrichment in SiO 2. The chemical characteristics of the Matsuura basalts are well accounted for by assuming open system fractional crystallization in a refilled magma chamber near the crust–mantle boundary. The chamber may have contained small amounts of water. It seems probable that the open system fractional crystallization operative under high pressure conditions can transform low alkali tholeiitic primitive magmas through weakly nepheline-normative basalt compositions finally to the convergent composition of hypersthene-normative basaltic andesite.

Petrology and geochemistry of the Kruuse Fjord Gabbro Complex, East Greenland

The Kruuse Fjord Gabbro Complex is a composite intrusion of layered gabbro and troctolite with subordinate ultramafic rocks and minor trondhjemitic bodies. It was emplaced into Archaean continental crust of East Greenland during early Tertiary rifting of Greenland from Eurasia. The work to date has identified an outer gabbro series and an inner troctolite series, and these are separated by a narrow zone of trondhjemitic intrusions. In the southeast, the partially crystallized cumulates of the gabbro series were intruded by a lenticular, ultramafic pluton 800 m in thickness. Volumetrically minor, syenite–trachyandesite net-veined dykes and later, diabase dykes cross-cut the plutonic rocks. Structural and topographic features suggest that the layered rocks were affected by synmagmatic subsidence and deformation but not by monoclinal coastal flexure.The gabbro series is composed of a marginal gabbro unit, about 20 m wide, bordering more than a 2 km thickness of layered olivine and magnetite gabbro cumulates. The marginal gabbro is interpreted to be chilled magma. The layered cumulates are the product of repeated injections of magma that fractionated in an open-system magma chamber. Anorthositic and troctolitic layers in the lower part of the sequence may represent inputs of magma and suggest that the order of cumulus mineral crystallization was (1) plagioclase (An39–85), (2) olivine (Fo46–82), (3) augite (Wo28–47En39–58Fs8–18 ) and (4) magnetite. The disappearance of cumulus magnetite and a reversal in mineral compositions at 1.5 km from the base of the succession suggests a major input of magma occurred at this height. In the troctolite series, the composition of cumulus minerals, mineral crystallization sequence and style of emplacement are similar to those in the gabbro series. The ultramafic pluton is composed of coarse-grained wehrlite, olivine melagabbro and troctolite that were formed by at least three injections of magma. The typical mineral crystallization sequence was (1) cumulus chromite and olivine (Fo84–88); (2) poikilitic chrome diopside (Wo29–51En43–63Fs3–13 ); and (3) intercumulus plagioclase (An75–90), phlogopite, apatite and localized disseminated sulphides containing Au and platinum-group elements.Comparison of crystallization sequences and the major and trace element compositions of clinopyroxene suggests that the gabbroic and troctolitic rocks formed from a magma represented by the chilled marginal gabbro, a tholeiitic basalt magma similar to E-MORB, whereas the ultramafic rocks formed from a magma that was relatively enriched in incompatible trace elements and volatiles. The association of these two magma types is an example of bimodal mafic–ultramafic magmatism in a rifting environment.

Melt and Aqueous Series of Silicate Crystallization Displayed by Chemical-Potential Diagrams

Bowen's series of silicate-mineral growth from melts can be deduced easily from the effect of the stoichiometry of the initial olivine on the composition of the residual melt, which then has to give rise to other silicates less “wasteful” of oxygen. The same series can also be deduced from qualitative chemical-potential diagrams, themselves easy to construct from appropriate mineral-composition diagrams. Similar diagrams also yield mineral-crystallization sequences from aqueous solutions. Chemical-potential diagrams are a sound and very easy pedagogical tool to connect geochemistry with petrology in all kinds of environments and rocks.

Geological affinities of the Glenelg river complex, western Victoria

A detailed comparison between the Glenelg River Complex in the Wando Vale district of western Victoria and the South Australian Kanmantoo Group of the Mt Lofty Ranges reveals many common elements. As the basis of comparison the geology of Wando Vale is described concisely with emphasis on its magmatic and structural history. Both have similar metasedimentary rocks, which are siliciclastically dominated with a substantial calcareous component. Geochemically, these rocks are relatively rich in CaO and Na2O, and compositionally distinct from the mature turbidites of the Lachlan Orogenic Belt. Four deformational episodes are identified in the Glenelg River Complex and are comparable to the history of the Kanmantoo Group in the Tungkillo‐Palmer region. The regional metamorphic zonation of both units extends into the amphibolite facies and is of the andalusite‐sillimanite type with similar mineral crystallization sequences. Tholeiitic dykes with comparable timing, the geochemical affinities of mid‐ocean ridge b...

An ocean-ridge type magma chamber at a passive volcanic, continental margin: the Kap Edvard Holm layered gabbro complex, East Greenland

AbstractThe gabbros of the Tertiary Kap Edvard Holm Layered Serieshave a stratigraphic thickness of more than 5000 m. Earlier work has shown that the range in cumulus mineral compositions is restricted (plagioclase An81—An51; olivine Fo85—Fo66; pyroxenes Ca43Mg46Fe11 to Ca43Mg37Fe20). Field evidence of magma injections is common, which together with the restricted range in mineral chemistry suggests that the magma chamber was frequently replenished by a less fractionated magma. A detailed study of a 600 m section (900–1500 m) in the Lower Layered Series reveals a period of crystallization when the magma chamber behaved as a closed system (900–1300 m). The rocks formed during this periodare well-laminated olivine–gabbros (900–110 m), which evolved to well-laminated oxide-gabbros (1100–1300 m). Compositional trends in the cumulusminerals are towards more evolved compositions (plagioclase An64—An58, pyroxene Mg# from 80 to 76) with stratigraphic height. From 1300 m to 1500 m, granular olivine-gabbros dominate, with moreprimitive mineral compositions (plagioclase An67—An76, pyroxene Mg# from 78 to 82). The transition olivine–gabbro to oxide-gabbro at 1100m is a consequence of fractional crystallization, and it is shown how changes in activities of FeO and Fe203 in the magma are reflected in the total iron content of plagioclases.The transition from oxide-gabbro to olivine-gabbro at 1300 m results from replenishment by less evolved basaltic magma. On the basis of calcic pyroxene chemistry and the mineral crystallization sequence it is concluded that the Kap Edvard Holm Layered Series crystallized from a tholeiitic magma similar to MORB. Melanogabbroic units occur throughout the intrusion as discordant to subconcordant sill-like bodies 0.2–2.0 m thick. The melanogabbroic units consist of Cr-rich augite-olivine-plagioclase heteradcumulates and contain deformed mica crystals of pre-emplacement origin. These units crystallized from a wet, MgO-rich magma which was injected into the layered host gabbros after the formation of the cumulus pile, but before the magma was completely solidified.The Kap Edvard Holm Layered Series has several parallels with the plutonic part of ophiolite sequences. These include: cumulus mineral assemblage, compositions of the minerals and the restricted range in compositions with stratigraphic height; field evidence of repeated replenishment of basaltic magma; dyke swarms overlying the roof zone of the magma chamber; and the existence of a late intrusive suite of wet, MgO-rich magma. These parallels suggest that the processes involved in the formation of the Kap Edvard Holm Layered Series were similar to those involved in the formation of the crustalpart of many ophiolites and beneath present-day spreading ridges. The Kap Edvard Holm Layered Series is therefore believed to represent a shallow-level magma chamber which acted as a reservoir for basaltic flows at the continental margin during the opening of the North Atlantic Ocean.

Strontium isotopic resolution of magma dynamics in a layered intrusion.

Kalka is one of about 14 major layered mafic-ultramafic intrusions forming the Giles Complex in central Australia1. The stratigraphical section of the Kalka Intrusion passes from a basal pyroxenite zone (450 + m) through norite and olivine gabbro zones (3,500 m) to an uppermost anorthosite zone (800 + m)2. Further resolution into 21 cyclic units is derived from repeated mineral crystallization sequences and cyclical variation in plagioclase and olivine compositions. A conventional interpretation would have a basaltic magma progressively fractionating as crystallization proceeded from mafic base to leucocratic top, with periodic resetting to less evolved states by fresh incursions of primary magma or by convectional overturn within a sealed magma chamber. However, the reconnaissance isotopic data reported here indicate development of a more complex open system. High initial 87Sr/86Sr ratios in conjunction with normal 143Nd/144Nd ratios demonstrate massive contamination by country rock within the main part of the intrusion3. Furthermore, great variation in Sr initial ratios from 0.7049 to 0.7088 suggests substantial changes in magma composition beyond those induced by fractionation. Similar isotopic heterogeneity in the Newer Gabbros of Scotland4 and the Bushveld Complex5 has been attributed to variable contamination or the emplacement of magma batches of differing composition.