Identification and Simultaneous Optimisation of Tunisian Clay Properties: Preliminary Study for the Ceramic Products

The relationship between composition and physical parameters such as specific surface area, cationic exchange capacity and plasticity is studied with the aim of developing regression models that would permit the prediction of clay properties. These models could be useful for mineralogists and industrial applications. Nineteen representative clay samples were collected from Jebel Ressas in north-eastern Tunisia. Mineralogical data show that clay samples cover a very large variety of minerals. The main clay mineral is illite (50–60 wt%), secondary minerals including quartz, calcite and minor amounts of Na-feldspar. This study reveals that the average amount of silica (SiO₂) and alumina (Al₂O₃) are 51.9 and 19.6 wt%, respectively. The contents of lime (CaO) and iron (Fe₂O₃) vary between 4 and 8 wt% whereas the amount of alkalis (Na₂O + K₂O) is on average 4.1 wt%. The grain size data indicates a significant amount of silt fraction, and the fraction <2 µm varies between 23 and 35 wt%. Values for plasticity index range from 16 to 28 wt%. The cation exchange capacity and the specific surface values are 34.1–45.7 meq/100 g of air-dried clay and 302–374 m²/g, respectively. Lastly, regression models are used to correlate the properties with the mineralogical and chemical compositions. The significance and the validity of models were confirmed by statistical analysis and verification experiments. The regression models can be used to select the clay properties (plasticity index, cation exchange capacity and specific surface) in relation with clay minerals proportions and the finer fraction amounts.     

Rheological characteristics of mixed kaolin–sand slurry,impacts of pH,temperature, solid concentration and kaolin–sand mixing ratio

Significant amount of slurry waste is produced from mineral processing plants globally constituting high levels of both kaolin and sand in aqueous suspension. Large quantities of slurry and mine tailings require efficient handling, transportation and storage system. The transportation and treatment of kaolin–sand slurry is dependent on its rheological behaviour which is a function of temperature, total solid concentration and pH. In this study, the effects of total solid concentration, pH and temperature on rheological behaviour of kaolin–sand mixture were investigated. These parameters were varied to analyse the viscosity, yield stress, flow index and shear force requirements of the mixed kaolin–sand suspension as a function of these varying parameters. Experimental rheological investigation conducted on rotational stress-controlled rheometer equipped with Peltier concentric cylinder system showed that the kaolin–sand mixture suspension is shear thickening in nature. The shear stress-rate rheograms for the kaolin–sand suspension can be modelled by the Herschel–Bulkley model with high levels of accuracy for pH range of 4–11, temperature range of 20–50 °C and solid concentration of 5–50 %. Solid concentration of the suspension was found to significantly affect the rheological behaviour of the mixture where higher kaolin–sand slurry concentration resulted in greater viscosity and the trend becoming less predictable for solid concentration greater than 50 % by weight. pH was another factor affecting the rheological behaviour of kaolin–sand slurry. pH of 3 or less resulted in the dramatic increase of viscosity of the suspension possibly due to the isoelectric point of the mixture system found between pH of 3 and 4.     

Constraints from melt inclusions and their host olivines on the petrogenesis of Oligocene-Early Miocene Xindian basalts, Chifeng area, North China Craton

The geochemical characteristics of melt inclusions and their host olivines provide important information on the processes that create magmas and the nature of their mantle and crustal source regions. We report chemical compositions of melt inclusions, their host olivines and bulk rocks of Xindian basalts in Chifeng area, North China Craton. Compositions of both bulk rocks and melt inclusions are tholeiitic. Based on petrographic observations and compositional variation of melt inclusions, the crystallizing sequence of Xindian basalts is as follows: olivine (at MgO > ~5.5 wt%), plagioclase (beginning at MgO = ~5.5 wt%), clinopyroxene and ilmenite (at MgO < 5.0 wt%). High Ni contents and Fe/Mn ratios, and low Ca and Mn contents in olivine phenocrysts, combining with low CaO contents of relatively high MgO melt inclusions (MgO > 6 wt%), indicate that Xindian basalts are possibly derived from a pyroxenite source rather than a peridotite source. In the CS-MS-A diagram, all the high MgO melt inclusions (MgO > 6.0 wt%) project in the field between garnet + clinopyroxene + liquid and garnet + clinopyroxene + orthopyroxene + liquid near 3.0 GPa, further suggesting that residual minerals are mainly garnet and clinopyroxene, with possible presence of orthopyroxene, but without olivine. Modeling calculations using MELTS show that the water content of Xindian basalts is 0.3–0.7 wt% at MgO = 8.13 wt%. Using 20–25 % of partial melting estimated by moderately incompatible element ratios, the water content in the source of Xindian basalts is inferred to be ≥450 ppm, much higher than 6–85 ppm in dry lithospheric mantle. The melting depth is inferred to be ~3.0 GPa, much deeper than that of tholeiitic lavas (<2.0 GPa), assuming a peridotite source with a normal mantle potential temperature. Such melting depth is virtually equal to the thickness of lithosphere beneath Chifeng area (~100 km), suggesting that Xindian basalts are derived from the asthenospheric mantle, if the lithospheric lid effect model is assumed.     

Apatite-hosted melt inclusions from the Panzhihua gabbroic-layered intrusion associated with a giant Fe–Ti oxide deposit in SW China: insights for magma unmixing within a crystal mush

The ～?2-km-thick Panzhihua gabbroic-layered intrusion in SW China is unusual because it hosts a giant Fe–Ti oxide deposit in its lower zone. The deposit consists of laterally extensive net-textured and massive Fe–Ti oxide ore layers, the thickest of which is ～?60 m. To examine the magmatic processes that resulted in the Fe enrichment of parental high-Ti basaltic magma and the formation of thick, Fe–Ti oxide ore layers, we carried out a detailed study of melt inclusions in apatite from a ～?500-m-thick profile of apatite-bearing leucogabbro in the middle zone of the intrusion. The apatite-hosted melt inclusions are light to dark brown in color and appear as polygonal, rounded, oval and negative crystal shapes, which range from ～?5 to ～?50 µm in width and from ～?5 to ～?100 µm in length. They have highly variable compositions and show a large and continuous range of SiO₂ and FeO_t with contrasting end-members; one end-member being Fe-rich and Si-poor (40.2 wt% FeO_t and 17.7 wt% SiO₂) and the other being Si-rich and Fe-poor (74.0 wt% SiO₂ and 1.20 wt% FeO_t). This range in composition may be attributed to entrapment of the melt inclusions over a range of temperature and may reflect the presence of µm-scale and immiscible Fe-rich and Si-rich components in different proportions. Simulating results for the motion of Si-rich droplets within a crystal mush indicate that Si-rich droplets would be separated from Fe-rich melt and migrate upward due to density differences in the interstitial liquid when the magma unmixed. Migration of the Si-rich, immiscible liquid component from the interstitial liquid caused the remaining Fe-rich melt in the lower part to react with plagioclase primocrysts (An_59–60), as evidenced by fine-grained lamellar intergrowth of An-rich plagioclase (An_79–84)?+?clinopyroxene in the oxide gabbro of the lower zone. Therefore, magma unmixing within a crystal mush, combined with gravitationally driven loss of the Si-rich component, resulted in the formation of Fe-rich, melagabbro and major Fe–Ti oxide ores in the lower part and Si-rich, leucogabbro in the upper part of the intrusion.     

Uranium-rich accessory minerals in the peraluminous and perphosphorous Belvís de Monroy pluton (Iberian Variscan belt)

The strongly peraluminous, perphosphorous (<0.85 wt% P₂O₅) and low-Ca granites from the Belvís de Monroy pluton contain the most U-rich monazite-(Ce) and xenotime known in igneous rocks. Along with these accessory minerals, P-rich zircon occurs, reaching uncommon compositions particularly in the more fractionated units of this zoned pluton. Monazite displays a wide compositional variation of UO₂ (<23.13 wt%) and ThO₂ (<19.58 wt%), positively correlated with Ca, Si, P, Y and REE. Xenotime shows a high UO₂ content (2.37–13.34 wt%) with parallel increases of LREE, Ca and Si. Zircon contains comparatively much lower UO₂ (<1.53 wt%) but high P₂O₅ (<14.91 wt%), Al₂O₃ (<6.96 wt%), FeO (<2.93 wt%) and CaO (<2.24 wt%) contents. The main mechanism of incorporating large U and Th amounts in studied monazite and U in xenotime is the cheralite-type [(Th,U)⁴⁺ + Ca²⁺ = 2(Y,REE)³⁺] substitution. Zircon requires several coupled mechanisms to charge balance the P substitution, resulting in non-stoichiometric compositions with low analytical totals. Compositional variations in the studied accessory phases indicate that the substitution mechanisms during crystal growth depend on the availability of non-formula elements. The strong P-rich character of the studied granites increases monazite crystallization, triggering a progressive impoverishment in Th and LREE in the residual melts, and consequently increasing extraordinarily the U content in monazite and xenotime. This is in marked contrast to other peraluminous (I-type or P-poor S-type) granite series. The P-rich and low-Ca peraluminous melt inhibits uraninite crystallization, so contributing to the U availability for monazite and xenotime.     

Delineation of groundwater prospective zones from a delta region of India,using geoelectrical and water quality approach

Geoelectrical survey was carried out in the western delta region of River Vasista Godavari, Andhra Pradesh, India, for delineation of groundwater prospective zones due to acute shortage of water supply for various purposes. Forty-six vertical electrical soundings (VES) were done, employing the Schlumberger configuration with a maximum AB/2 of 160 m. The interpreted results of VES show four to five layers with variable thicknesses, such as topsoil zone (1.5–3 m), clay zone (0.84–32 m), finer sand zone (2–72 m), medium to coarse sand zone (4 to 28.8 m) and clay zone (1.2–∞ m), indicating a multi-aquifer system. These results are corroborated with the known lithologs of the study area. Further, the resistivity is also compared with electrical conductivity (EC) of groundwater observed nearby shallow wells representing buried channel (BC), flood plain (FP) and coastal (C) zones, which indicate slightly brackish to brackish water (EC: 1470–6010 µS/cm), whereas the groundwater observed from deep wells shows the fresh (EC: 726–1380 µS/cm), fresh to brackish (EC: 1010 to 3250 µS/cm), and brackish water (EC: 3020 to 4170 µS/cm) located in BC, FP and C zones, respectively. This survey reveals the prospective aquifer zones with potable water at VES locations of 4–6, 8, 10, 11, 14, 16–28, 33–36, 39 and 42–44, where the resistivity values vary from 10 to 40 Ω m. The slightly brackish and brackish water zones are also observed from the resistivity of less than 10 Ω m at shallow depth in BC (VES-22, 37, 38 and 46), FP (VES-1, 2, 7, 29, 30 and 40) and C (VES-3, 4, 9, 12, 13, 15, 31, 32, 41 and 45) zones. As a result, the present investigation has delineated the freshwater zones at shallow (<?12 m) and also at deeper depths (30–45 m) as prospective areas, where BC zone occurs. Freshwater pockets also identified in FP (VES-8 and 39) and C (VES-11, 14 and 15) zones. Thus, this study helps to solve the drinking and irrigation water problems.     

Density and visco-elasticity of Natrosol 250 HH solutions: Determining their suitability for experimental tectonics

Analogue models often require that materials with specific physical properties be engineered to satisfy scaling conditions. To achieve this goal we investigate the rheology of aqueous solutions of Natrosol 250 HH, a rheology modifier employed in various industries to thicken viscous solutions. We report the rheological properties as functions of the concentration and temperature and discuss the advantages and limitations of these materials in view of their use in analogue modelling experiments. The solutions are linear visco-elastic for low stresses (or strain-rates), becoming shear-thinning for larger stresses. For the typically slow analogue experiments of tectonics, the solutions can be considered linear visco-elastic with a Maxwell relaxation time much smaller than the characteristic observation time. This simplification is even more appropriate when the solutions are employed at temperatures higher than 20 °C, since the solutions then display a behaviour that is more viscous, less elastic at the same shear-rate, while the Newtonian viscosity reduces and the shear-rate limit between Newtonian and shear-thinning behaviours increases. The Newtonian viscosity is shown to increase non-linearly with concentration and decrease non-linearly with temperature. With concentrations between 0 and 3% and temperature between 20 and 40 °C, the viscosity varied between 10⁻¹ and 4000 Pa s, while the density remained close to the density of water. Natrosol 250 HH thus offers the possibility to control the viscosity of a solution without significantly affecting the density, thereby facilitating the design and setup of analogue experiments.     

Primary melt from Sannome-gata volcano,NE Japan arc: constraints on generation conditions of rear-arc magmas

The conditions under which rear-arc magmas are generated were estimated using primary basalts from the Sannome-gata volcano, located in the rear of the NE Japan arc. Scoriae from the volcano occur with abundant crustal and mantle xenoliths, suggesting that the magma ascended rapidly from the upper mantle. The scoriae show significant variations in their whole-rock compositions (7.9–11.1 wt% MgO). High-MgO scoriae (MgO > ~9.5 wt%) have mostly homogeneous ⁸⁷Sr/⁸⁶Sr ratios (0.70318–0.70320), whereas low-MgO scoriae (MgO < ~9 wt%) have higher ⁸⁷Sr/⁸⁶Sr ratios (>0.70327); ratios tend to increase with decreasing MgO content. The high-MgO scoriae are aphyric, containing ~5 vol% olivine microphenocrysts with Mg# [100 × Mg/(Mg + Fe²⁺)] of up to 90. In contrast, the low-MgO scoriae have crustal xenocrysts of plagioclase, alkali feldspar, and quartz, and the mineralogic modes correlate negatively with whole-rock MgO content. On the basis of these observations, it is inferred that the high-MgO scoriae represent primary or near-primary melts, while the low-MgO scoriae underwent considerable interaction with the crust. Using thermodynamic analysis of the observed petrological features of the high-MgO scoriae, the eruption temperature of the magmas was constrained to 1,160–1,220 °C. Given that the source mantle was depleted MORB-source mantle, the primary magma was plausibly generated by ~7 % melting of a garnet-bearing spinel peridotite; taking this into consideration, and considering the constraints of multi-component thermodynamics, we estimated that the primary Sannome-gata magma was generated in the source mantle with 0.5–0.6 wt% H₂O at 1,220–1,230 °C and at ~1.8 GPa, and that the H₂O content of the primary magma was 6–7 wt%. The rear-arc Sannome-gata magma was generated by a lower degree of melting of the mantle at greater depths and lower temperatures than the frontal-arc magma from the Iwate volcano, which was also estimated to be generated by ~15 % melting of the source mantle with 0.6–0.7 wt% H₂O at ~1,250 °C and at ~1.3 GPa.     

El Chichón volcano, April 4, 1982: volcanic cloud history and fine ash fallout

This retrospective study focuses on the fine silicate particles (<62 µm in diameter) produced in a large eruption that was otherwise well studied. Fine particles represent a potential hazard to aircraft, because as simple particles they have very low terminal velocities and could potentially stay aloft for weeks. New data were collected to describe the fine particle size distributions of distal fallout samples collected soon after eruption. Although, about half of the mass of silicate particles produced in this eruption of ~1 km³ dense rock equivalent magma were finer than 62 µm in diameter, and although these particles were in a stratospheric cloud after eruption, almost all of these fine particles fell to the ground near (<300 km) the volcano in a day or two. Particles falling out from 70 to 300 km from the volcano are mostly <62 µm in diameter. The most plausible explanation for rapid fallout is that the fine ash nucleates ice in the convective cloud and initiates a process of meteorological precipitation that efficiently removes fine silicates. These observations are similar to other eruptions and we conclude that ice formation in convective volcanic clouds is part of an effective fine ash removal process that affects all or most volcanic clouds. The existence of pyroclastic flows and surges in the El Chichón eruption increased the overall proportion of fine silicates, probably by milling larger glassy pyroclasts.     

Climatic implications of loess deposits from the Beijing region

Variations in magnetostratigraphy, pedostratigraphy, grain size and magnetic susceptibility of the loess deposits near Beijing have been studied at two sections. The sections are about 400 km east of the main loess deposits in China, have a maximum thickness of 100 m and extend back to 1.1 Ma. The sequence consists of 14 loess–palaeosol couplets (S0‐S14), which correlate well with sequences in the Loess Plateau. Susceptibility records from the sites near Beijing are comparable to the Xifeng, Luochuan and Baoji sections located in the middle part of the Loess Plateau; however, the down‐core variations in the grain size in the Upper Lishi Formation exhibit some differences. The median grain size increases by about 25–30 µm from L4 to L2, with the sandy grains (>63 µm) increasing from 10–20 wt% to 40–50 wt% . This implies that the depositional environment of the dust sources in the Beijing loess section is different in some aspects from the Loess Plateau. The Beijing loess may have had a different dust source than the Loess Plateau. Copyright © 2001 John Wiley & Sons, Ltd.     

Rapid pre-eruptive thermal rejuvenation in a large silicic magma body: the case of the Masonic Park Tuff,Southern Rocky Mountain volcanic field,CO, USA

Determining the mechanisms involved in generating large-volume eruptions (>100 km³) of silicic magma with crystallinities approaching rheological lock-up (~50 vol% crystals) remains a challenge for volcanologists. The Cenozoic Southern Rocky Mountain volcanic field, in Colorado and northernmost New Mexico, USA, produced ten such crystal-rich ignimbrites within 3 m.y. This work focuses on the 28.7 Ma Masonic Park Tuff, a dacitic (~62–65 wt% SiO₂) ignimbrite with an estimated erupted volume of ~500 km³ and an average of ~45 vol% crystals. Near-absence of quartz, titanite, and sanidine, pronounced An-rich spikes near the rims of plagioclase, and reverse zoning in clinopyroxene record the reheating (from ~750 to >800?°C) of an upper crustal mush in response to hotter recharge from below. Zircon U–Pb ages suggest prolonged magmatic residence, while Yb/Dy vs temperature trends indicate co-crystallization with titanite which was later resorbed. High Sr, Ba, and Ti concentrations in plagioclase microlites and phenocryst rims require in-situ feldspar melting and concurrent, but limited, mass addition provided by the recharge, likely in the form of a melt-gas mixture. The larger Fish Canyon Tuff, which erupted from the same location ~0.7 m.y. later, also underwent pre-eruptive reheating and partial melting of quartz, titanite, and feldspars in a long-lived upper crustal mush following the underplating of hotter magma. The Fish Canyon Tuff, however, records cooler pre-eruptive temperatures (~710–760?°C) and a mineral assemblage indicative of higher magmatic water contents (abundant resorbed sanidine and quartz, euhedral amphibole and titanite, and absence of pyroxene). These similar pre-eruptive mush-reactivation histories, despite differing mineral assemblages and pre-eruptive temperatures, indicate that thermal rejuvenation is a key step in the eruption of crystal-rich silicic volcanics over a wide range of conditions.     

Polycyclic aromatic hydrocarbons (PAHs) in particle-size fractions of urban topsoils

Polycyclic aromatic hydrocarbons’ (PAHs) concentrations in bulk samples are commonly used to assess contamination but PAHs are unevenly distributed among particle-size fractions. Seventeen urban surface soil samples from the city of Xuzhou, China, were collected and then fractionated into five size fractions (2,000–300, 300–150, 150–75, 75–28, and <28 μm). The concentrations of 12 US EPA PAHs were measured using gas chromatograph/mass spectrometry in various fractions, and the bulk soil samples and distribution patterns of PAHs in different particle-size fractions were investigated. The mean concentration of total PAHs in bulk soil samples was 1,879 ng/g. The median concentrations for all individual PAH were higher for the 75–2,000 μm fraction than for the <75 μm fraction. The distribution factors for various PAHs in <28 μm soil fraction were closely correlated (r = ?0.661, p < 0.019) to bulk soil fugacity capacity. The values of PAH isomer indicated that traffic emissions might be the major origin of PAHs in Xuzhou surface soils. Spearman correlation analysis was performed and the result suggested that soil organic carbon might be a factor controlling the concentrations of PAHs in soils.     

Regional geochemical baseline concentration of potentially toxic trace metals in the mineralized Lom Basin,East Cameroon: a tool for contamination assessment

The distribution of trace metals in active stream sediments from the mineralized Lom Basin has been evaluated. Fifty-five bottom sediments were collected and the mineralogical composition of six pulverized samples determined by XRD. The fine fraction (<?150 µm) was subjected to total digestion (HClO₄?+?HF?+?HCl) and analyzed for trace metals using a combination of ICP-MS and AAS analytical methods. Results show that the mineralogy of stream sediments is dominated by quartz (39–86%), phyllosilicates (0–45%) and feldspars (0–27%). Mean concentrations of the analyzed metals are low (e.g. As?=?99.40 µg/kg, Zn?=?573.24 µg/kg, V?=?963.14 µg/kg and Cr?=?763.93 µg/kg). Iron and Mn have significant average concentrations of 28.325 and 442 mg/kg, respectively. Background and threshold values of the trace metals were computed statistically to determine geochemical anomalies of geologic or anthropogenic origin, particularly mining activity. Factor analysis, applied on normalized data, identified three associations: Ni–Cr–V–Co–As–Se–pH, Cu–Zn–Hg–Pb–Cd–Sc and Fe–Mn. The first association is controlled by source geology and the neutral pH, the second by sulphide mineralization and the last by chemical weathering of ferromagnesian minerals. Spatial analysis reveals similar distribution trends for Co–Cr–V–Ni and Cu–Zn–Pb–Sc reflecting the lithology and sulphide mineralization in the basin. Relatively high levels of As were concordant with reported gold occurrences in the area while Fe and Mn distribution are consistent with their source from the Fe-bearing metamorphic rocks. These findings provide baseline geochemical values for common and parallel geological domains in the eastern region of Cameroon. Although this study shows that the stream sediments are not polluted, the evaluation of metal composition in environmental samples from abandoned and active mine sites for comparison and environmental health risk assessment is highly recommended.     

Phytoplankton Functional Groups in a Tropical Estuary: Hydrological Control and Nutrient Limitation

Hydrology and nutrients have been indicated as the main driving factors acting on phytoplankton biomass and composition in estuarine systems, although grazing may occasionally have some influence. In order to identify these factors over temporal and spatial scales, we analyzed physical, chemical, and biological properties of a tropical river-dominated estuary during the dry and rainy seasons. As far as we know, this is the first time that the functional groups approach has been used to analyze the changes in phytoplankton composition in an estuary. This recent framework is based on the tolerances and sensitivities in relation to environmental conditions of groups of species, which are labeled by alpha-numeric codes (Reynolds et al., J. Pl. Res. 24:417–428, 2002). In the estuary of Paraíba do Sul River, all phytoplankton groups were represented by freshwater organisms, indicating the strong influence of the river. However, remarkable shifts in composition and biomass occurred from the low to high flushing seasons, due much more to the river discharge than to nutrient availability. The overall results showed no nitrogen, phosphorus, or silica limitation to phytoplankton growth (mean values: dissolved inorganic nitrogen?=?30.5 µM, soluble reactive phosphorus?=?1.45 µM, and silica?=?208.05 µM). The higher river flow supports a lower phytoplankton biomass composed mainly of nanoplankton (<20 µm) fast-growing functional groups, which are able to maintain biomass even in high flushing conditions (X₁), or large heavy organisms, such as some heavy diatoms of group P, which are able to be in suspension in shallow and turbulent systems. The lower river flow led to the coexistence of large organisms (>20 µm) of the groups P and F, which include slow-growing populations typically found in mesotrophic lakes. Although the functional group approach was originally developed for temperate lakes, our data support this approach for a tropical estuarine environment.     

Fractional crystallization of primitive,hydrous arc magmas: an experimental study at 0.7 GPa

Differentiation of mantle-derived, hydrous, basaltic magmas is a fundamental process to produce evolved intermediate to SiO₂-rich magmas that form the bulk of the middle to shallow continental and island arc crust. This study reports the results of fractional crystallization experiments conducted in a piston cylinder apparatus at 0.7 GPa for hydrous, calc-alkaline to arc tholeiitic magmas. Fractional crystallization was approached by synthesis of starting materials representing the liquid composition of the previous, higher temperature experiment. Temperatures ranged from near-liquidus at 1,170 °C to near-solidus conditions at 700 °C. H₂O contents varied from 3.0 to more than 10 wt%. The liquid line of descent covers the entire compositional range from olivine–tholeiite (1,170 °C) to high-silica rhyolite (700 °C) and evolves from metaluminous to peraluminous compositions. The following crystallization sequence has been established: olivine → clinopyroxene → plagioclase, spinel → orthopyroxene, amphibole, titanomagnetite → apatite → quartz, biotite. Anorthite-rich plagioclase and spinel are responsible for a marked increase in SiO₂-content (from 51 to 53 wt%) at 1,040 °C. At lower temperatures, fractionation of amphibole, plagioclase and Fe–Ti oxide over a temperature interval of 280 °C drives the SiO₂ content continuously from 53 to 78 wt%. Largest crystallization steps were recorded around 1,040 °C and at 700 °C. About 40 % of ultramafic plutonic rocks have to crystallize to generate basaltic–andesitic liquids, and an additional 40 % of amphibole–gabbroic cumulate to produce granitic melts. Andesitic liquids with a liquidus temperature of 1,010 °C only crystallize 50 % over an 280 °C wide range to 730 °C implying that such liquids form mobile crystal mushes (<50 % crystals) in long-lived magmatic systems in the middle crust, allowing for extensive fractionation, assimilation and hybridization with periodic replenishment of more mafic magmas from deeper magma reservoirs.     

The role and conditions of second-stage mantle melting in the generation of low-Ti tholeiites and boninites: the case of the Manihiki Plateau and the Troodos ophiolite

High-Mg, low-Ti volcanic rocks from the Manihiki Plateau in the Western Pacific share many geochemical characteristics with subduction-related boninites such as high-Ca boninites from the Troodos ophiolite on Cyprus, which are believed to originate by hydrous re-melting of previously depleted mantle. In this paper we compare the Manihiki rocks and Troodos boninites using a new dataset on the major and trace element composition of whole rocks and glasses from these locations, and new high-precision, electron microprobe analyses of olivine and Cr-spinel in these rocks. Our results show that both low-Ti Manihiki rocks and Troodos boninites could originate by re-melting of a previously depleted lherzolite mantle source (20–25% of total melting with 8–10% melting during the first stage), as indicated by strong depletion of magmas in more to less incompatible elements (Sm/Yb < 0.8, Zr/Y < 2, Ti/V < 12) and high-Cr-spinel compositions (Cr# > 0.5). In comparison with Troodos boninites, the low-Ti Manihiki magmas had distinctively lower H₂O contents (< 0.2 vs. > 2 wt% in boninites), ~ 100 °C higher liquidus temperatures at a given olivine Fo-number, lower fO₂ (ΔQFM < + 0.2 vs. ΔQFM > + 0.2) and originated from deeper and hotter mantle (1.4–1.7 GPa, ~ 1440 °C vs. 0.8–1.0 GPa, ~ 1300 °C for Troodos boninites). The data provide new evidence that re-melting of residual upper mantle is not only restricted to subduction zones, where it occurs under hydrous conditions, but can also take place due to interaction of previously depleted upper mantle with mantle plumes from the deep and hotter Earth interior.     

Pink manganian phengite in a high P/T meta-conglomerate from northern Syros (Cyclades, Greece)

A new occurrence of Mn-rich rocks was discovered within the high-pressure/low-temperature metamorphic rocks on the Palos peninsula of Syros (Greece). Near the summit of Mount Príonas, a meta-conglomerate consists of calcite (~63 wt%), pink manganian phengite, blue–purple manganian aegirine–jadeite, microcline, albite and quartz. In addition, it contains abundant braunite-rich aggregates (up to ~1.5 cm in diameter) that include hollandite [(Ba_0.98–1.02K_<0.01Na_<0.02Ca_<0.03) (Mn _1.02–1.52 ³⁺ Fe _0.38–0.88 ³⁺ Ti_0.29–0.92Mn _5.11–5.76 ⁴⁺ )O₁₆], barite and manganian hematite. Due to metamorphic recrystallization and deformation, the contacts between clasts and matrix are blurred and most clasts have lost their identity. In back-scattered electron images, many aegirine–jadeite grains appear patchy and show variable jadeite contents (Jd_10–67). These pyroxenes occur in contact with either quartz or albite. Manganian phengite (3.41–3.49 Si per 11 oxygen anions) is of the 3T type and contains 1.4–2.2 wt% of Mn₂O₃. At the known P–T conditions of high-pressure metamorphism on Syros (~1.4 GPa/ 470 °C), the mineral sub-assemblage braunite + quartz + calcite (former aragonite) suggests high oxygen fugacities relative to the HM buffer (+7 ≤ ?f_O2 ≤ + 17) and relatively high CO₂ fugacities. The exact origin of the conglomerate is not known, but it is assumed that the Fe–Mn-rich and the calcite-rich particles originated from different sources. Braunite has rather low contents of Cu (~0.19 wt%) and the concentrations of Co, Ni and Zn are less than 0.09 wt%. Hollandite shows even lower concentrations of these elements. Furthermore, the bulk-rock compositions of two samples are characterized by low contents of Cu, Co and Ni, suggesting a hydrothermal origin of the manganese ore. Most likely, these Fe–Mn–Si oxyhydroxide deposits consisted of ferrihydrite, todorokite, birnessite, amorphous silica (opal-A) and nontronite. Al/(Al + Fe + Mn) ratios of 0.355 and 0.600 suggest the presence of an aluminosilicate detrital component.     

Lake Boga Granite,northwestern Victoria: mineralogy,geochemistry and geochronology

The Devonian Lake Boga Granite in northern Victoria, while almost entirely under thin Murray Basin cover, is one of the largest plutons in the western Lachlan Fold Belt. Its only exposure is a quarry penetrating the Cenozoic sediments. In the quarry, prominent pod pegmatites and miarolitic cavities suggest a high level of emplacement. The granite, a non-magnetic, fractionated S-type, contains a large range of accessory minerals, including primary uranium- and REE-bearing phosphates and oxides, and primary copper sulfides. Monazite-series minerals show an exceptionally wide range of compositions, from normal monazite-(Ce) through cheralite (Ca – Th-rich) to rare huttonitic monazite (Th-rich) and brabantite; U contents in monazite also vary widely (0 – 7.9 wt%). Primary low-Ca uraninites are well preserved and are unusual in having low Th/U and LREE. Late-stage cavity fluorapatite crystals up to several centimetres across show intricate elemental zoning patterns with extreme U gradients (<10 – 6900 ppm) in some crystals. New ⁴⁰Ar – ³⁹Ar ages for magmatic biotite, muscovite and K-rich feldspar average 365 ± 3 Ma, which approximates the emplacement age of the granite. This is supported by a 377 ± 12 Ma U – Th – Pb (CHIME) age for primary uraninite. New whole-rock geochemical data support earlier observations: the granite is strongly fractionated (SiO₂ 70.7 – 76.0 wt%; 4.2 – 0.6 wt% FeO_t) and peraluminous (ASI = 1.23 – 1.45), and has slightly elevated Na₂O and P₂O₅ (0.30 wt%) contents compared with other fractionated S-type granites from the Lachlan Fold Belt. Trace-element abundances are typical of fractionated granites, although U and Cu concentrations vary strongly and reach >60 and ≈1400 ppm, respectively. REE patterns also vary strongly, from LREE-enriched with moderate Eu depletion, to flat with strong Eu depletion. The flattest of the REE patterns, in samples with FeO_total < 1%, are characterised by M-type tetrad effects. These and other samples also show low (subcrustal average) and variable Zr/Hf (35 – 16) and Nb/Ta (8 – 4) ratios; these and other unusual elemental fractionations are related to changes in elemental partitioning during the late magmatic stage, when felsic peraluminous magma and high-temperature magmatic fluid coexisted.     

Dissolution channels in quartz and the role of pressure changes in gold and sulfide deposition in the Archean, greenstone-hosted, Hutti gold deposit, Karnataka, India

The pressure, temperature and composition of ore fluids that resulted in gold deposition in the Archean, greenstone-hosted Hutti deposit have been studied using fluid inclusions and the compositions of arsenopyrite and chlorite. Five types of fluids have been identified in fluid inclusions in quartz veins associated with mineralization. They are (1) monophase CO ₂-rich fluid; (2) low-salinity (0 to 14 wt% NaCl equivalent) and high-salinity (16 to 23 wt% NaCl equiv.) aqueous fluids; (3) high-salinity (28 to 40 wt% NaCl equiv.), polyphase aqueous fluids; (4) CO ₂–H ₂O–NaCl fluids of low salinity (0–8 wt% NaCl equiv.); and (5) a few carbonic inclusions with halite±nahcolite. The diversity of entrapped fluid composition is explained in terms of changes in fluid pressure and temperature which affect a more or less uniform supply of primary low-salinity CO ₂–H ₂O–NaCl fluid to the shear zone. Geothermobarometric studies indicate that during mineralization temperature ranged between 360 and 240 °C, and fluid pressure between 3,600 and 1,600 bar. The data are interpreted in terms of the cyclic fault-valve mechanism for active shear zones. Deposition of gold and sulfides has been studied on the basis of constraints from the composition of wall-rock chlorite, ore-mineral assemblages, and textural features. Tubular channels, 20 to 100 µm wide and up to 500 µm long that arise from fractures and C-planes in sheared quartz veins are reported for the first time. The channels have pyrrhotite, arsenopyrite, pyrite and gold at their distal ends, with calcite filling up the remaining part. These channels form in response to increases in T and P, by dissolution of quartz grains, guided by dislocations in them. At the P– T conditions of interest, gold and sulfide deposition takes place in the shears and fractures of quartz veins from CO ₂–H ₂O–NaCl ore fluid of low salinity and pH due to changes in phase compositions that occur during the process of shear failure of the enclosing rocks. In the wall rock where pH is buffered, gold deposition takes place from the predominant Au(HS) ₂ ^- species with progressive sulfide deposition and decrease in SS, from 0.01 to 0.001 mol/kg as T falls from 360 to 240 °C.     

Cell Size-Dependent Effects of Solar UV Radiation on Primary Production in Coastal Waters of the South China Sea

In order to examine the effects of solar ultraviolet radiation (UVR, 280–400 nm) on photosynthesis of differently cell-sized phytoplankton, natural phytoplankton assemblages from the coastal waters of the South China Sea were separated into three groups (>20, 5–20, and <5 μm) and exposed to four different solar UV spectral regimes, i.e., 280–700 nm (PAR?+?UVR), 400–700 nm (PAR), 280–400 nm (UV-A?+?B), and 315–400 nm (UV-A). In situ carbon fixation measurements revealed that microplankton (>20 μm) efficiently utilized UV-A for photosynthetic carbon fixation, with assimilation number of up to 1.01 μg C (μg chl a)^?1?h^?1 under 21.4 W?m^?2 UV-A alone (about half of noontime irradiance at the surface), about 40 % higher than nanoplankton (5–20 μm). UV-B (280–315 nm) of 0.95 W?m^?2 reduced the carbon fixation by approximately 20 and 57 % in microplankton and nanoplankton assemblages, respectively. In contrast, smaller picoplankton (<5 μm) was unable to utilize UV-A for the photosynthetic carbon fixation. In addition, only micro-sized assemblages demonstrated the UV enhancement on their primary productivity in the presence of PAR, by about 8 % under moderate intensities of solar radiation.