The occurrences of sepiolite beds and nodules in alkaline and saline Miocene Eskisehir lake deposits provide unique examples of ancient lacustrine environments. Stockwork-type magnesite deposits, which were formed very close to the Miocene lake, served as parent rocks for sepiolite nodules (meerschaum). The Miocene succession consists of calcareous clay, clayey carbonate, dolomite, a gypsum-bearing calcareous clay series, siliceous tuffs, sepiolite beds, sepiolite-bearing dolomite, and basal conglomerates of ultramafic rocks. Sepiolite beds were deposited by direct precipitation from Si-supersaturated lake water under alkaline and saline conditions. They are underlain by a gypsum series. Organic matter-rich sepiolites suggest the presence of water stratification with anoxic bottom waters, which developed due to high sulphate input at the base from the ascending hydrothermal solutions along the fracture systems with extensive fresh water input near to the surface. Sepiolite nodules resulted from diagenetic replacement of magnesite pebbles at shallow burial under alkaline conditions in the vicinity of paleo-shorelines. Sepiolite beds were deposited in three ways: 1) black (up to 2.8 wt. % TOC) sepiolite beds rich in organic matter accumulated in an anaerobic paleoenvironment; 2) brown (about 0.5 wt. % TOC) sepiolite beds poor in organic matter, containing minor amounts of white, 2–6 mm long, discontinuous, and very soft dolomite laminae formed in a dysaerobic paleoenvironment; and 3) white dolomitic sepiolite beds in which dolomite content is about 20–40% in an aerobic paleoenvironment.

Cyclic dolomite and gypsum series indicate hypersaline-evaporative paleoenvironments with rapid changes in lake water chemistry. These cyclic evaporatic conditions are also related to cyclic changes in water depth. Based on X-ray powder diffraction data, except degree of crystallinity, no mineralogic difference was found between sepiolite in beds and nodules. SEM studies revealed fibers about 0.2 µm wide and up to 30 µm long in sepiolite beds; crystals less than 5 µm long with bent tips; and a more compacted appearance in sepiolite nodules.

Magnesite pebbles in Miocene lacustrine conglomerates in northwest Turkey have been partially to totally replaced by sepiolite. Only 5% of the magnesite pebbles have been converted to essentially pure sepiolite; the rest represent mixtures of magnesite and sepiolite. This process of sepiolitization is documented by X-ray diffraction (XRD), chemical, scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) techniques. These techniques show that the sepiolitization proceeds from the rim towards the core of the pebbles. The conglomerates, with pebbles of magnesite and ultramafic rocks, were deposited in a near-shore environment on the margin of a large Miocene lake with an ophiolitic substratum. The diagenetic transformation of magnesite to sepiolite is believed to have been caused by the interaction of mixed meteoric and lacustrine waters, which were undersaturated with respect to magnesite. The sepiolitization occurred during the highstands of the lake, when the near-shore conglomerates were flooded by the silica-rich lake waters. The pH of the water during the sepiolitization was probably on the order of 10.5–11.5. The sedimentary magnesite beds in the center of the Miocene basin show no sepiolitization, which is explained by the presence of pore water saturated with respect to magnesite.

The magnesite-sepiolite replacement process is chemically modeled as a 4-stage process from dimerization to polymerization.

Çayırbağı magnesite is one of numerous magnesite deposits occurring throughout Turkey. In this deposit, sepiolite and newly found stevensite occur locally as two daughter minerals formed from magnesite. The sepiolite and stevensite show distinctive compositions and modes of formation compared to those described in the literature. The objective of the current study was to characterize these minerals by means of mineralogic, thermal, structural, geochemical, and textural analyses and to describe their mechanisms of formation. The geology, mineralogy, and geochemistry were examined by field work followed by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), differential thermal (DTA), and thermogravimetric (TG) analyses. Chemical analyses were performed by means of electron microprobe (EMPA), inductively coupled plasma-optical emission spectrometry (ICP-OES), and laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). The XRD analyses showed that the d110 of the sepiolite was at 12.64 Å and at 13 Å after air-drying and ethylene-glycol solvation, respectively. Identification of the sepiolite as sepiolite-13 Å was supported by FTIR and TG-DTA data. Chemical analyses showed an ideal composition with a structural formula of (Ca0.05K0.02)(Mg7.79Al0.10□0.11)Si12O30(OH)4. Stevensite displayed distinctive results for XRD, FTIR, and thermal characteristics. The structural formula of stevensite was: (Ca0.01Na0.20K0.04)(Mg1.90Al0.30Fe3+0.37Ti0.01□0.43)(Si3.93Al0.07)O10(OH)2, indicating a layer charge arising mainly from octahedral sheets. Field and SEM observations demonstrated that sepiolite was formed from magnesite by transformation via a dissolution–precipitation mechanism. Descending surface waters were responsible for this transformation. Thick magnesite veins were partly replaced whereas in thin veins sepiolite replaced the overall mass. Both surface waters with high Si, low Al and Fe activities, and pH values of 8–9.5 were responsible for sepiolite formation. Stevensite was formed similarly to sepiolite with respect to the mechanism and parent mineral under permanent groundwater; where both Si, Fe, Al activities and pH (>9.5) were high.

The saponite examined occurs as two 0.1 m thick layers in a Pliocene sequence consisting of dolomite and dolomitic marl. To characterize this material, mineralogical and structural analyses (XRD, SEM and FTIR), thermal analyses (DTA, TG) and chemical analyses (ICP-ES) were performed. From XRD patterns of randomly-oriented powder samples, the first basal reflection appears as an asymmetric and broad peak with d001 values varying between 16.55 and 17.32 Å. In oriented and air-dried samples, this reflection occurs between 14.45 and 16.42 Å and is fairly symmetrical with FWHM of 2.7º2θ. Oriented and ethylene glycol-solvated samples produce a rational series of basal reflections, where 001 occurs at ~17.8 Å as an intense, narrow (1.1º2θ) and fairly symmetrical reflection. Upon solvation with glycerol, the 001 reflection shifts to ~18.7 Å.

The chemical composition of this saponite is similar to stevensite. However, the structural formula of Na0.114Ca0.013K0.003(Mg2.957Al0.004Fe0.028Ti0.004)(Si3.826Al0.174)O10(OH)2 indicates that vacancies in the octahedral sheet do not exist. The negative layer charge arises nearly entirely from the substitutions in the tetrahedral sheet, with the net layer charge of –0.148, smaller than for common smectites.

Due to the XRD characteristics and particularly the layer-charge distribution, it was concluded that this mineral is a Mg-rich saponite with low layer charge. The saponite was formed by direct precipitation in an alkaline lake environment from Mg- and Si-rich solutions at high pH.

Recognition of widespread carbonate volcanism in central Spain has led to another case in France, of similar age (23–0 Ma) but with entirely new features. More than 100 new carbonate volcanoes are indicated already, adding a wholly unexpected dimension to this form of activity. Eruptions form layers, mostly of glassy nephelinite fragments in a dolomitic matrix, but some layers are largely dolomite. Major new findings are phenocrysts of dolomite, magnesite and calcite in silicate glass, and spectacular dolomite-nephelinite melt immiscibility, neither recorded previously. Most volcanic carbonatites are Ca rich, and dolomite is rare. The Limagne dolomites share links with those in Spain and Zambia, with chromite a hallmark in all three. Limagne is exceptional in being the first case where dolomite has erupted with co-genetic silicate melt. Mantle debris and magnesite indicate a source within ∼ 100–150 km. Chromite in the dolomite globules, and in the enclosing silicate glass, is similar to that in high-temperature kimberlites, indicating immiscibility in the deep mantle. Recognition of two large, previously undetected provinces of carbonate volcanism in Europe, where there has been active research for >200 y, must lead to the inference that similar cases may await discovery on other continents.

Two types of gold can be distinguished in tetrahedrite from the Veitsch magnesite deposit, Austria. Primary gold present in unfractured massive tetrahedrite, has a grain size up to 18 μm and contains, on average, Cu 8.73, Ag 7.01, Au 78.63 and Hg 2.35 (wt.%). Secondary gold is present in fractures and is directly intergrown with digenite, covellite, Cu-thiosulphate, cuprite and chrysocolla but not with malachite or azurite. The secondary gold is up to 200 µm in size with an average composition of Cu 3.06, Ag 6.82, Au 86.41 and Hg 3.51 (wt.%). It is usually closely intergrown with thiosulphates containing up to 0.21 wt.% Au. This, together with the presence of ‘dirty’ gold with cloudy thiosulphate inclusions, directly indicates the transport and deposition of Au by a thiosulphate ligand. We believe this is the first reported direct evidence of gold transport and deposition by thiosulphate complexes in a natural environment.

Marbles and interlayered coesite-bearing eclogites near the village ofSanqingge in the Sulu ultrahighpressure (UHP) terrane ofeastern China were studied to estimate their P-T evolution. Using garnet, omphacite and phengite as geothermobarometers, the coesite eclogites are calculated to have experienced P-T conditions of3.4 –3.7 GPa and ~600ºC (stage I), followed by decompression and a slight temperature decrease to 2.7–3.2 GPa and 520–560ºC respectively (stage II) and later to 2.6–2.8 GPa and ~500ºC (stage III). No water influx affected the eclogites until reaching amphibolite facies conditions of 0.5–1.3 Gpa and 595–685ºC (stage IV). As we interpret the occasional appearance ofcalcite with magnesite relics in the core as a reaction ofUHP dolomite and magnesite with Ca-rich fluids at stage IV to form CaCO3, the calculated pressure for stage I could be the maximum pressure experienced by these rocks. Thus, the crustal material ofthe Sanqingge quarry, originally sedimentary carbonates (now marbles) and interstratified basic tuffs (now eclogites), has been buried to a depth of ≥ 120 km at ~600ºC. This burial occurred in a subduction setting along a very low geotherm of 5–6ºC/km. The exhumation possibly occurred in the environment ofa subduction channel.

Carbonates of the magnesite-siderite series have been found and analysed in carbonatites from the Lueshe, Newania, Kangankunde, and Chipman Lake complexes. This series has been represented until now only by a few X-ray identifications of magnesite and three published analyses of siderite and breunnerite (magnesian siderite). Most of the siderite identified in carbonatites in the past has proved to be ankerite, but the new data define the complete solid-solution series from magnesite to siderite. They occur together with dolomite and ankerite and in one rock with calcite. The magnesites, ferroan magnesites and some magnesian siderites may be metasomatic/hydrothermal in origin but magnesian siderite from Chipman Lake appears to have crystallized in the two-phase calcite + siderite field in the subsolidus CaCO3-MgCO3-FeCO3 system. Textural evidence in Newania carbonatites indicates that ferroan magnesite, which co-exists with ankerite, is a primary liquidus phase and it is proposed that the Newania carbonatite evolved directly from a Ca-poor, Mg-rich carbonatitic liquid generated by partial melting of phlogopite-carbonate peridotite in the mantle at pressures >32 kbar.

The process of transforming hydromagnesite to magnesite is analysed in the context of the theory of solvent-mediated transformations. A series of experiments at 120, 150 and 180ºC with different heating times was designed to determine, by powder X-ray diffraction, the amount of magnesite generated as a function of time. The aqueous-phase composition was monitored by inductively coupled plasma-mass spectrometry and carbonate alkalimetry. From the analytical data, the evolution of saturation indexes with respect to both phases was determined using the geochemical code PHREEQC. Finally, two different methods were applied to obtain the activation energy of the process and a TTT (Temperature- Transformation-Time) graph was constructed to define suitable conditions in which to obtain magnesite.

The magma source and evolution of a zoned breccia pipe on the southern Beara Peninsula in southwest Ireland are investigated using the geochemistry of the host mineral assemblages. The clast-poor inner zone of the pipe has a magnesium-rich silicocarbonatite whole-rock composition (14.30 wt.% MgO; 31.80 wt.% SiO2). The silicocarbonatite has retained an ultimate mantle source 13C isotopic composition after metamorphism, consistent with the presence of mantle debris. The silicocarbonatite is Cr-, Ni- and Co-rich (847 ppm, 611 ppm and 60 ppm, respectively) but REE depleted compared with volcanic dolomite carbonatites worldwide. The mineral assemblage consists of Sr-rich (0.55 wt.% SrO) ferroan dolomite, magnesite and pseudomorphs of chlorite after phlogopite, consistent with derivation from a carbonated and hydrated mantle. However, chrome spinel crystals (≤4 40.14 wt.% Cr2O3) are compositionally indistinguishable from unmetasomatized spinel macrocrysts in kimberlites. The silicocarbonatite is inferred to represent a magma produced by partial melting of metasomatized mantle at physical conditions between those in which primary dolomite carbonatite and ultramafic magmas of high-pressure origin form. The primary silicocarbonatite magma ascended and sampled mantle material in a manner similar to kimberlite, and subsequently lost volatile components due to release of metasomatic fluids and later metamorphism.

An Early Pliocene sedimentary succession in the Yenidoğan area, Sivrihisar, Turkey, consists of sepiolite, stevensite, kerolite, dolomite and magnesite. The geology, mineralogy and geochemistry of the succession was examined by extensive field work along several trenches and a representative measured section, followed by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermal, and chemical analyses.

Structurally, two distinct forms of sepiolites were distinguished by XRD: (a) well crystallized sepiolite with a 110 reflection at 12.07–12.3 Å , and (b) poorly crystallized sepiolite in which the 110 reflection occurs at 12.7–13.0 Å (denoted as sepiolite-13Å ). Differences in crystal chemistry, thermal and morphological properties of these forms, the vibrational spectra and XRD characterization of the related phyllosilicates were also documented.

Stevensite, kerolite and sepiolite were formed by direct precipitation from alkaline lake water rich in Mg and Si. Sepiolite-13Å was probably formed by transformation from precursor smectite via dissolution-precipitation, more likely during early diagenesis. Environmental conditions such as ion concentration, salinity and variations in pH may have controlled the formation of the phyllosilicates.

The objective of this work was to determine the apparent bioavailability of magnesium from four different types of calcined magnesites of Greek origin. These four types (A, B, C, D) were different in particle size fractions and production process. The solubility of the above four magnesium samples and their fractions were determined: (a) in the laboratory using ammonium nitrate solution after 24-h shaking and (b) in vivo using a nylon bag technique after 24-h incubation.

Solubility was correlated with apparent bioavailability as determined in a balance experiment with five wether sheep in a 5×5 Latin-square design.

Sheep were kept in metabolism cages and were given daily a basal diet (500 g hay + 700 g concentrate) plus 2 g magnesium supplements from types A to D. The magnesium bioavailability of the basal diet was used as a base for the determination of the bioavailability of magnesium in A, B, C and D supplements.

Magnesium apparent bioavailability of the basal diet was found to be 0·203 and, for the supplements A, B, C and D, 0·381, 0·339, 0·315 and 0·292 respectively. The solubility of supplements A, B, C and D in ammonium nitrate solution and in vivo (using the nylon-bag technique) was found to be 0·812, 0·805, 0·784 and 0·773 or 0·294, 0·152, 0·102 and 0·200 respectively.

The solubilities of the magnesium supplements in ammonium nitrate solution and in vivo both reflected dietary bioavailability differences up to a point, but neither was well enough correlated with the apparent bioavailability as determined by the balance experiment, this being judged to be the most precise method for bioavailability determination.

Serpentinites are a major component in a distinctive suite of metasedimentary and metamorphosed igneous rocks, the Outokumpu association, in the early–middle Proterozoic Svecokarelides of eastern Finland. Like the adjacent mica schists and associated supracrustal rocks, they show the effects of at least six phases of deformation (D1–D6). The tectonic history began with the emplacement of the Outokumpunappe (pre-D1), but a study of relict assemblages in the serpentinites and theirenvelope rocks reveals evidence for a complex pre-nappe history involving ultramaficmagmatism with extensive high-temperature hornfels development, and low-temperature serpentinisation contributing to sea-floor exhalation of sulphide ores.

The serpentinites subsequently underwent recrystallisation during several phases of regional metamorphism giving rise to mineral fabrics, including a pressure-solution initiated segregation (M1–D1), anthophyllite growth during the thermal climax (D2–M2—600–680°C, 2·5–4 kb), and steatitisation (D2c–M2c). Steatitisation is structurally controlled, occurring where serpentinite bodies impinge upon localised shear zones (wrench faults—D2c). Talc–carbonate–brucite assemblages reflect the influx of CO2 in this environment. Deformation during late metamorphic retrogression (greenschist—D3–D4) has a dichotomous expression with crenulations developed in strongly anisotropic phyllonitised serpentinite and irregular fracturesin massive rock.

The implications of such polyphase reconstitution for geochemical and isotopic studies are assessed and discussed.

Orthopyroxene- and kyanite-lineage eclogites are distinguished on the basis of silicate and carbonate petrography and chemistry. Different textural and chemical types of magnesite, dolomite and calcite can be satisfactorily attributed to one of the three sequential metamorphic stages of eclogite history at anhydrous eclogite facies, hydrous eclogite facies and amphibolite facies. The chronological sequence of development of magnesite, dolomite and calcite matches the carbonate sequence found experimentally in synthetic peridotite-CO2-H2O systems during decompression. Magnesite and dolomite show reasonably regular Fe/Mg distribution relationships with silicates.

A new geothermobarometer based upon is provisionally calibrated. It yields T estimates for given P very similar to those given by the geothermobarometer, e.g. 759–829°C at 20 kb and 803–894°C at 40 kb. P is tentatively estimated at 30±10, 23±6 and 10 ± 3 kb respectively for the three metamorphic stages.

Fluid conditions after equilibration during each stage were either low or fluid-absent, but not low . A unique quartz-magnesite-dolomite vein represents an influx of CO2 in the P-T regime of instability of CO2 + pyroxene. Tectonic emplacement by deep-level obduction of diverse foreign source materials remains the petrogenetic model which best fits the data for these eclogites.