Mineral Formation Processes Research Articles

The importance of the helical structure of a MamC-derived magnetite-interacting peptide for its function in magnetite formation.

Biomineralization is the process of mineral formation by organisms and involves the uptake of ions from the environment in order to produce minerals, with the process generally being mediated by proteins. Most proteins that are involved in mineral interactions are predicted to contain disordered regions containing large numbers of negatively charged amino acids. Magnetotactic bacteria, which are used as a model system for iron biomineralization, are Gram-negative bacteria that can navigate through geomagnetic fields using a specific organelle, the magnetosome. Each organelle comprises a membrane-enveloped magnetic nanoparticle, magnetite, the formation of which is controlled by a specific set of proteins. One of the most abundant of these proteins is MamC, a small magnetosome-associated integral membrane protein that contains two transmembrane α-helices connected by an ∼21-amino-acid peptide. In vitro studies of this MamC peptide showed that it forms a helical structure that can interact with the magnetite surface and affect the size and shape of the growing crystal. Our results show that a disordered structure of the MamC magnetite-interacting component (MamC-MIC) abolishes its interaction with magnetite particles. Moreover, the size and shape of magnetite crystals grown in in vitro magnetite-precipitation experiments in the presence of this disordered peptide were different from the traits of crystals grown in the presence of other peptides or in the presence of the helical MIC. It is suggested that the helical structure of the MamC-MIC is important for its function during magnetite formation.

The Role of Anionogenic Elements (As, Sb, Mo, Se, S, P, N, Cl, F, C) In The Formation of Technogenic Geochemical Anomalies

The study was conducted on the example of sulphide-containing mine tailings with a varying amount of sulphide and arsenide minerals, from three distinct tailings dumps situated in Russia: Karabash Mine Site, South Ural; Komsomolsk tailings impoundment, Kemerovo region; Khovu-Aksy mine site, Tuva Republic. The aim of the study was to compare the mobility of anionogenic elements (As, Sb, Mo, Se, S, P, N, Cl, F, C) and their role in migration, precipitation, and concentration of metals during the water-tailings interaction depending on the physicochemical parameters (pH, Eh) of the medium and the mineral composition of the waste material. Using slightly acidic leaching experiments the quantitative estimation of mobile forms of elements is given. Based on the compositions of the obtained water leaching solutions, aqueous speciation of chemical elements and saturation index of key minerals in the experimental solutions were calculated. The results of calculating forms of chemical elements made it possible to construct series of mobility of metals and metalloids in solutions with different physicochemical parameters. In the alkaline conditions, Sb>As>Cd>Cu>Zn>Fe>Pb, when the medium is acidified, the series changes, As>Cd>Cu>Zn>Pb>Sb>Fe; in weakly alkaline conditions, Sb>Mn>As>Zn>Fe; however, when the medium is acidified, the series changes to Cd>Mn>Pb>Cu>Zn>Sb>Ni>Fe>As; under acidic conditions Cd>Cu>Zn>Pb>Mn>Fe>Se>Mo>Sb>As>Ni. The mineral composition of the tailings was investigated, which will allow to determine the sources of toxic elements and to understand the processes of secondary mineral formation in technogenic objects. Arsenopyrite and pyrite predominate in the heavy fraction of the Komsomolsk tailings impoundment, arsenopyrite grains are often corroded, Sb contained in Sb oxide and Sb sulfide. The pyrite and barite are determined in the solid matter of the Karabash Mine Site and chalcopyrite, sphalerite, tennantite Cu3AsS3, and tetrahedrite (Cu,Fe)12Sb4S13 are determined in the form of inclusions in grains of pyrite.

Serpentinization of olivine at 300 °C and 500 bars: An experimental study examining the role of silica on the reaction path and oxidation state of iron

The generation of H2 during serpentinization of ultramafic oceanic crust along Earth's mid-ocean ridges provides a key energy source for the deep biosphere and has important implications for metal transport and mineral stability in the subseafloor hydrothermal system. Nonetheless, the driving forces and rates of the coupled processes of Fe partitioning and H2 generation during serpentinization are complicated by many factors, but especially, the activity of SiO2(aq) in the serpentinizing fluid. To examine the role of this key variable in H2 generation and Fe partitioning between magnetite and Fe-serpentine during serpentinization, San Carlos olivine was reacted with a NaCl-SiO2(aq)-bearing fluid at 300°C and 500bars for approximately 90days using flexible gold cell hydrothermal equipment. Time-series changes in solution chemistry and dissolved H2 are coupled with magnetic susceptibility, Mössbauer spectroscopy, and Fe isotope measurements of reactant olivine and coexisting alteration products to provide a complete description of Fe mass transfer and oxidation as a function of reaction progress. Utilization of talc as reactant not only provided a source of SiO2(aq) for serpentinization, but effectively prevented brucite formation, in keeping with constraints imposed by many natural hydrothermal systems, which are inherently open systems. Moreover, this experimental strategy allowed Fe derived from olivine dissolution to transfer completely to serpentine and magnetite, facilitating reaction path modeling. Initial changes in solution chemistry indicate “buffering” of dissolved SiO2(aq), owing to the apparently balanced rates of olivine dissolution and serpentine precipitation. During this stage of reaction, a negligible amount of H2 is generated, suggesting that Fe2+-serpentine is stable and the dominant Fe-bearing product. With continued reaction, the rate of SiO2(aq) production lessens likely due to reduction in surface area of talc, such that the continued hydration and hydrolysis of olivine titrates the previously buffered activity of SiO2(aq), eventually approaching serpentine-brucite coexistence. During this secondary stage of reaction, the rate of H2 generation abruptly increases, which reflects the formation of magnetite and Fe3+-serpentine. Temporal changes in the isotope composition of dissolved Fe, throughout these stages, likely reflect different mineral alteration and formation processes, where initially, 1) preferential mass transfer of isotopically light Fe into solution occurred during olivine alteration, without considerable oxidation, as demonstrated by the low H2 production rate, and, 2) the preferential removal of isotopically light Fe from solution in connection with enhanced magnetite and H2 formation during the later stages of reaction. Post experimental analysis of the Fe isotopic composition of Fe-bearing minerals demonstrates statistically negligible enrichment of δ56Fe of magnetite relative to olivine and serpentine, consistent with observations from natural altered oceanic crust. Observations from this study demonstrate the utility of using coupled chemical, isotopic, and analytical approaches to ascertain time series changes in rates of mass transfer and mechanisms of oxidation of Fe during serpentinization of olivine. Ultimately, these insights provide important constraints for the chemical and Fe isotopic evolution of fluids and minerals in ultramafic hosted hydrothermal systems at mid-ocean ridges.

Cd isotope fractionation during sulfide mineral weathering in the Fule Zn-Pb-Cd deposit, Yunnan Province, Southwest China

Zinc (Zn)-Lead (Pb) deposits are generally rich in cadmium (Cd), and the weathering of sulfide minerals in such deposits results in large releases of Cd into the environment. From an environmental and public health standpoint, understanding Cd sources and cycling is critical to identifying potential hazards to humans. In this study, the Cd isotope compositions (expressed as δ114/110Cd) of secondary minerals such as anglesite (−0.57±0.03‰; 2S.D.), granular smithsonite (0.04±0.14‰; 2S.D.), layered smithsonite (0.15±0.40‰; 2S.D.), hydrozincite (0.26±0.01‰; 2S.D.) and clay minerals (−0.01±0.06‰; 2S.D.) from the Fule Zn-Pb-Cd deposit, Southwest China, are investigated to better understand the Cd sources and cycling in this area.Combined with our previous study (Zhu et al., 2017), the work herein elucidates the patterns of Cd isotopic fractionation during the formation processes of such secondary minerals and traces the weathering of these minerals into the ecosystem. The δ114/110Cd values of secondary minerals exhibit the following decreasing trend: hydrozincite>large granular smithsonite>small granular smithsonite>anglesite. Although different amounts of Cd were lost during the formation of equally sized samples, no or minor variations in Cd isotopic composition were observed. However, significant isotopic differences were observed between different size fractions. These results demonstrate that the particle size of secondary minerals and weathering products of sulfide significantly influence Cd isotope composition and fractionation during natural weathering. This systematic fractionation provides an initial foundation for the use of Cd isotopes as environmental tracers in ecosystems and in the global Cd isotope budget.

Laboratory experiment and numerical simulation on authigenic mineral formation induced by seabed methane seeps

In natural gas hydrate marine settings, cold seepage of methane fluid is a widely observed phenomenon, where authigenic minerals serve as an indication of potential gas hydrate-bearing reservoirs at depth. In this study, based on the data from the site HD196 near Dongsha Island, northern continental slope of South China Sea, laboratory experiments and numerical simulation studies were conducted to investigate the biogeochemical processes of authigenic mineral formation induced by methane seepage. The bioreactor experimental results show that in response to methane flux, pH increased to 8.5 after 20 days of reaction, and Eh declined rapidly first and then remained unchanged at about 100 mV. The decrease in SO42−, HS− and HCO3− concentrations indicated the occurrence of anaerobic oxidation of methane coupled with sulfate reduction (AOM-SR). The depletion of Fe2+ implied the formation of iron-bearing minerals, e.g., iron sulfides. Carbonate minerals were also identified in the experimental phase of this study. Most iron sulfides existed as massive pieces, and in some cases as spherical or rod-shape pieces. The calcium carbonates were observed as blocky pieces. Numerical simulations were also performed to reproduce the biogeochemical reactions that occurred in the reactor experiments. Based on experimental data, kinetic parameters associated with the observed reactions were calibrated. The model simulated results are general consistent with those obtained by the experiments conducted in this study. The combination of simulation and experimental studies provided a powerful tool to investigate the biogeochemical processes in the methane leakage environment at different temporal and spatial scales. This study gave a new perspective to understand the formation of cold seep authigenic minerals in marine sediments, and was significant for future investigations on the effects of hydrate decomposition.

A model of basin evolution in the Qa’ Al-Azraq, Jordan using sulfur isotope analysis to distinguish sources of sulfur and gypsum

The closed basin of the Qa’ Al-Azraq, Jordan records gypsum and sulfur depositions. Analysis of the cored sediments used smear slides, isotope geochemistry of gypsum and sulfur, XRD, and SEM. This study distinguishes the sources of gypsum and sulfur in the basin from four different processes. Algae production was responsible for the presence of laminated sulfur at a depth of 48 m where paleolake levels were at a high stand. Primary gypsum, represented by laminated, thick massive beds, records sulfur isotope values of +15.7‰. This period of the paleolake indicates evaporation processes exceeded precipitation, leading to the deposition of thick, massive bed of gypsum. Other sources of gypsum originate from pyrite oxidation, indicated by the overlapping of sulfur isotope values of gypsum and pyrite at −0.7‰. Bassanite and anhydrite identified in this section resulted from dissolution and recrystallization processes. The application of sulfur isotopic analyses identifies environmental distinct formation processes of sulfate minerals in the Al-Azraq basin. This provides the basis for a model of basin evolution and associated changing climates. Finally, this research considers the effect of sulfate minerals on Al-Azraq basin groundwater.

Thermodynamic Aspects of Molluscan Shell Ultrastructural Morphogenesis

Over the years, molluscan shells have become an exemplar model system to study the process of mineral formation by living organisms, the process of biomineralization. Typically, the shells consist of a number of mineralized ultrastructural motifs, each exhibiting a specific mineral‐organic composite architecture. These are made of calcium carbonate building blocks having a well‐defined three‐dimensional morphology that is significantly different from the shape of inorganically formed counterparts. Shell ultrastructures are known to form via a biologically controlled extracellular mineralization pathway in which the organism has no direct control over mineral formation. The cellular tissue, responsible for shell biomineralization, forms an organic framework and sets‐up the physical conditions necessary for the deposition of a specific morphology, whereas the growth of the mineral part of the shell proceeds spontaneously via the process of self‐assembly. In this feature article, the ability to employ thermodynamic models from classical materials science to describe the process of self‐assembly and structural evolution of a variety of shell architectures is reviewed. Having the potential to offer an analytical framework to express ultrastructure formation in time and in space, these models not only provide a deeper insight into shell biomineralization, but also suggest tools for novel composite materials design.

Experimental formation of Pb, Sn, Ge and Sb sulfides, selenides and chlorides in the presence of sal ammoniac: A contribution to the understanding of the mineral formation processes in coal wastes self-ignition

The formation of sulfides, selenides and chlorides was experimentally studied at 800 or 900°C in the presence of sal ammoniac in sealed silica glass tubes. Synthetic PbS, PbSe, SnS, GeS, SnGeS2, PbSnS3, SnS, Sb2S3, and natural uraninite were used as substrates. Depending on the chemical composition of the sulfide/selenide charge, compounds corresponding to cotunnite, galena, herzenbergite, berndtite, ottemannite, stibnite, panichiite, and unnamed SnGeS3, SnSb2S4 and Sn2Sb3S6 phases were identified in sublimates. When natural uraninite in a mixture with sal ammoniac was used as a charge, the reaction produced abundant cotunnite and minor challacolloite due to volatilization of radiogenic lead. When sulfur was introduced to the charge with uraninite and sal ammoniac, galena was found in reaction products. Results of the experiments revealed that an addition of chlorine may contribute to the mobility of metals and metalloids in coal wastes self-burning processes.

Early diagenesis and authigenic mineral formation in mobile muds of the Changjiang Estuary and adjacent shelf

Abstract Large-river delta-front estuaries (LDEs) and their adjacent shelf margins are sites of dynamic diagenetic processes that play a significant role in coastal biogeochemical cycling. In this study, we used dissolved inorganic carbon (DIC), redox sensitive elements (Fe 2 + and Mn 2 + ), dissolved inorganic nitrogen (DIN) nutrients (NH 4 + , NO 3 − , and NO 2 − ), major cations and anions (K + , Ca 2 + , Mg 2 + , SO 4 2 − , and Cl − ) in bottom-water and sediment pore-waters, to investigate the early chemical diagenesis and authigenic mineral formation in mobile-mud deposits of the Changjiang Estuary and adjacent inner shelf of the East China Sea (ECS). Vertical profiles of DIC and NH 4 + in pore-waters had similar trends at most sites, showing a significant increase with depth near the Changjiang Estuary and being relatively constant at offshore sites. Higher pore-water DIC and NH 4 + concentrations were observed in nearshore sites in winter, which were likely attributed to exposure of deeper deposits by winter coastal erosion. Nitrification was observed at most sites, and AOB (ammonia-oxidizing bacteria) played a leading role in ammonia oxidation in the study areas. The nitrification-denitrification was likely important in contributing to the loss of DIN in offshore sites during summer. Large inputs of organic carbon (OC) and terrestrial materials from Changjiang River resulted in intense sulfate reduction and Fe and Mn reduction in nearshore sites. Lower C/N and C/S ratios coupled with an apparent decrease in pore-water Ca 2 + and Mg 2+ concentrations with depth near the Changjiang Estuary, which indicated that authigenic carbonate formation occurs in these sediments. Decreases in K + and Mg 2 + with depth reflected that reverse weathering was an important process of authigenic mineral formation in these sediments. We conclude that adsorption process, seasonal erosion-redeposition, and summer hypoxic conditions of bottom-waters may play an important role in early diagenesis processes and remineralization of SOC in the Changjiang LDE.

Retrieving the hydrous minerals on Mars by sparse unmixing and the Hapke model using MRO/CRISM data

The hydrous minerals on Mars preserve records of potential past aqueous activity. Quantitative information regarding mineralogical composition would enable a better understanding of the formation processes of these hydrous minerals, and provide unique insights into ancient habitable environments and the geological evolution of Mars. The Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) has the advantage of both a high spatial and spectral resolution, which makes it suitable for the quantitative analysis of minerals on Mars. However, few studies have attempted to quantitatively retrieve the mineralogical composition of hydrous minerals on Mars using visible-infrared (VISIR) hyperspectral data due to their distribution characteristics (relatively low concentrations, located primarily in Noachian terrain, and unclear or unknown background minerals) and limitations of the spectral unmixing algorithms. In this study, we developed a modified sparse unmixing (MSU) method, combining the Hapke model with sparse unmixing. The MSU method considers the nonlinear mixed effects of minerals and avoids the difficulty of determining the spectra and number of endmembers from the image. The proposed method was tested successfully using laboratory mixture spectra and an Airborne Visible Infrared Imaging Spectrometer (AVIRIS) image of the Cuprite site (Nevada, USA). Then it was applied to CRISM hyperspectral images over Gale crater. Areas of hydrous mineral distribution were first identified by spectral features of water and hydroxyl absorption. The MSU method was performed on these areas, and the abundances were retrieved. The results indicated that the hydrous minerals consisted mostly of hydrous silicates, with abundances of up to 35%, as well as hydrous sulfates, with abundances ≤10%. Several main subclasses of hydrous minerals (e.g., Fe/Mg phyllosilicate, prehnite, and kieserite) were retrieved. Among these, Fe/Mg- phyllosilicate was the most abundant, with abundances ranging up to almost 30%, followed by prehnite and kieserite, with abundances lower than 15%. Our results are consistent with related research and in situ analyses of data from the rover Curiosity; thus, our method has the potential to be widely used for quantitative mineralogical mapping at the global scale of the surface of Mars.

The influence of additives of distilled liquids, containing NAСL and СAСL2 on the process of mineralformation at roasting of sulphate containing blend

The influence of additives of distilled liquids, containing NAСL and СAСL2 on the process of mineralformation at roasting of sulphate containing blend

A study on sintering of ceramic bricks made from waste coal

The results of the study on phase transformations and structure formation during firing of bricks made from wastes of coaly argillite processing. The effect of firing temperature on the processes of mineral formation and changes in the quantitative content of amorphous phase and brick porosity was defined. It was found that at 950-1050 °C the sintering takes place providing a solid brick structure.

End‐member identification and spectral mixture analysis of CRISM hyperspectral data: A case study on southwest Melas Chasma, Mars

AbstractWe present spectral unmixing results over the southwest Melas Chasma region, where a variety of hydrated minerals were identified. We use the Discrete Ordinate Radiative Transfer radiative transfer model to simultaneously model Mars atmospheric gases, aerosols, and surface scattering and retrieve the single‐scattering albedos (SSAs) modeled by the Hapke bidirectional scattering function from Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) data. We employ a spectral unmixing algorithm to quantitatively analyze the mineral abundances by modeling the atmospherically corrected CRISM SSAs using a nonnegative least squares linear deconvolution algorithm. To build the spectral library used for spectral unmixing, we use the factor analysis and target transformation technique to recover spectral end‐members within the CRISM scenes. We investigate several distinct geologic units, including an interbedded polyhydrated and monohydrated sulfate unit (interbedded unit 1) and an interbedded phyllosilicate‐sulfate unit (interbedded unit 2). Our spectral unmixing results indicate that polyhydrated sulfates in the interbedded unit 1 have a much lower abundance (~10%) than that of the surrounding unit (~20%) and thus may have been partially dehydrated into kieserite to form the interbedded strata, supporting a two‐staged precipitation‐dehydration formation hypothesis. In the interbedded unit 2 phyllosilicates have an abundance of ~40% and are interbedded with ~20% sulfates. The results, in combination with thermodynamic calculations performed previously, suggest that the interbedded phyllosilicates and sulfates likely formed through coupled basalt weathering and evaporation. The methodology developed in this study provides a powerful tool to derive the mineral abundances, aiming to better constrain the formation processes of minerals and past aqueous environment on Mars.

In Situ Biomineralization and Particle Deposition Distinctively Mediate Biofilm Susceptibility to Chlorine.

Microbial biofilms and mineral precipitation commonly co-occur in engineered water systems, such as cooling towers and water purification systems, and both decrease process performance. Microbial biofilms are extremely challenging to control and eradicate. We previously showed that in situ biomineralization and the precipitation and deposition of abiotic particles occur simultaneously in biofilms under oversaturated conditions. Both processes could potentially alter the essential properties of biofilms, including susceptibility to biocides. However, the specific interactions between mineral formation and biofilm processes remain poorly understood. Here we show that the susceptibility of biofilms to chlorination depends specifically on internal transport processes mediated by biomineralization and the accumulation of abiotic mineral deposits. Using injections of the fluorescent tracer Cy5, we show that Pseudomonas aeruginosa biofilms are more permeable to solutes after in situ calcite biomineralization and are less permeable after the deposition of abiotically precipitated calcite particles. We further show that biofilms are more susceptible to chlorine killing after biomineralization and less susceptible after particle deposition. Based on these observations, we found a strong correlation between enhanced solute transport and chlorine killing in biofilms, indicating that biomineralization and particle deposition regulate biofilm susceptibility by altering biocide penetration into the biofilm. The distinct effects of in situ biomineralization and particle deposition on biocide killing highlight the importance of understanding the mechanisms and patterns of biomineralization and scale formation to achieve successful biofilm control.

Geochemical features of Kulunda plain lakes (Altay region, Russia)

Geochemical specifics of lake water of the Kulunda Steppe territory (Altay region, Russia) are studied. The results show that in the territory mainly chloride and less soda lakes with sodium compound are developed. It is presented that calcite and soda saturation indexes (SI) of lake water increase with growth of pH, but decrease in such minerals as gypsum and barite. The opposite situation is typical for SI depending on the salinity. It is revealed that evaporation, secondary mineral formation and various biological processes have the greatest impact on accumulation of elements in solution.

Post - sedimentation influence on filtration capacity reservoir rock properties (Pur-Tazov oil\\gas-bearing area)

The processes of the second mineral formation (kaolinite, carbonates and micas) were identified during the post-sedimentation transformation studies in oil\\gas deposits. Besides, quartz regeneration, solid product destructive formation processes and hydrocarbon oxidation processes were -determined. Correlation analysis of the mineralogy and petrophysics data revealed the post-sedimentation influence factors on the reservoir properties of deposits. It should be noted that the second kaolinite composition increase results in water saturation and density decrease, porosity and, especially, permeability increase. Quartz regeneration and second mica formation deteriorate the reservoir properties or poorly influence them. The hydrocarbon decay and oxidation products, as well as secondary carbonate seal the void space, replace the soluble rock debris and sharply deteriorate the reservoir properties of oil andgas deposits.

Mass fluxes and clay mineral formation in soils developed on slope deposits of the Kowarski Grzbiet (Karkonosze Mountains, Czech Republic/Poland)

Weathering, mineral formation, and transformation processes along slopes are complex. In cool mountainous regions, undisturbed soil development with a strong vertical leaching element may abruptly change as a result of erosion, accumulation, lateral water fluxes and aeolian input. We investigated soils in the eastern Karkonosze Mountains that have developed on silicatic slope deposits. To date, illite, vermiculite and chlorite are the minerals that have been detected in the clay fraction. Although the climate and parent material should be favourable for the formation of smectites, expandable phases were not verified so far. We investigated if expandable phases could be detected and how they related to elemental fluxes along a short slope sequence (1142–1268ma.s.l. on the border between the Czech Republic and Poland). Mass balance calculations indicated intensive mineral weathering together with a significant leaching of Mg, Al, Ca and Mn on the shoulder and foot slope positions. In the middle zone, which has a concave or undulating surface shape, however, the mass balances of several elements (Na, K, Al, P) revealed a less pronounced leaching (corresponding to a lower degree of podsolization) and in some cases even accumulation. At all sites, mass balance calculations and detected soil minerals (e.g. the increase in illite towards the surface together with an increase in Al and K) indicate some aeolian input. Kaolinite was detected in all soil horizons. Its concentration slightly increased towards the soil surface. Together with the pronounced leaching of Ca, part of kaolinite originates from plagioclase weathering. Besides being a weathering product of primary minerals, part of the kaolinite is inherited from the parent material and probably is also due to aeolian input. In all soils, illite was being transformed into vermiculite and smectites (through regularly-interstratified illite-smectite phases). In addition, the content of chloritic components which increases with depth indicated their concurrent weathering and transformation into smectites. Amphibole also may have acted as a source of smectites. Not all smectite is being actively formed in the soil. Most likely due to slope processes (cover beds) that affected even the subsoil, some smectite has been transferred along the slope. Part of the smectite also seems to derive from the parent material. Active formation of expandable clay minerals is related to convex and planar landscape forms. This relationship suggests intense element leaching, inheritance from the parent material and cover bed mixing processes have contributed to the presence of smectite. Along the slope, zones with predominant vertical transport (shoulder, foot slopes) may repeatedly be interchanged with zones dominated by lateral transport (undulating slope, concave forms).

Silicate versus carbonate weathering in Iceland: New insights from Ca isotopes

Several studies have measured riverine fluxes of Ca and carbonate alkalinity in Iceland with the aim of quantifying the role of basalt weathering in the long-term carbon cycle. A major assumption is that all of the Ca and alkalinity originates from the dissolution of Ca-bearing silicate minerals, such as plagioclase and clinopyroxene. However, hydrothermal calcite occurs throughout Iceland, and even trace levels are expected to impact river geochemistry owing to the mineral's high solubility and fast dissolution rate. To test this hypothesis, we used a new, high-precision Ca isotope MC-TIMS method (δ44/40Ca; 2σSD=±0.04‰) to trace sources of Ca in Icelandic rivers. We report elemental and Ca isotope data for rivers, high- and low-temperature groundwater, basalt, hydrothermal calcite (including Iceland Spar), and stilbite and heulandite, which are two types of zeolites commonly formed during low-grade metamorphism of basalt. In agreement with previous research, we find that rivers have higher δ44/40Ca values than basalt, with a maximum difference of ∼0.40‰. This difference may reflect isotope fractionation in the weathering zone, i.e., preferential uptake of 40Ca during clay mineral formation, adsorption, and other geochemical processes that cycle Ca. However, calcite δ44/40Ca values are also up to ∼0.40‰ higher than bedrock values, and on a diagram of δ44/40Ca versus Sr/Ca, nearly all waters plot within a plausible mixing domain bounded by the measured compositions of basalt and calcite, with glacial rivers plotting closer to calcite than non-glacial rivers. Calcite and heulandite form during hydrothermal alteration of basalt in the deep lava pile and often occur together in metabasalts now exposed at the surface. Because heulandite δ44/40Ca values are ∼1–2‰ lower than basalt, we suggest that 40Ca uptake by heudlandite explains the relatively high δ44/40Ca values of calcite and that calcite weathering in turn elevates riverine δ44/40Ca values. High mechanical erosion rates are known to facilitate the exposure and weathering of calcite, which explains the isotopic contrast between glacial and non-glacial watersheds. Using a mixing model, we find that calcite weathering provides ∼0–65% of the Ca in non-glacial rivers and ∼25–90% of the Ca in glacial rivers, with silicate weathering providing the remainder. Icelandic hydrothermal calcite contains mantle carbon. Noting that zeolite facies metamorphism and hydrothermal fluid circulation are ubiquitous characteristics of basaltic eruptions and assuming that hydrothermal calcite in other basaltic settings also contains mantle carbon, we suggest that the contribution of basalt weathering to long-term CO2 drawdown and climate regulation may be less significant than previously realized.

The Major Types of the Weathering Crust of the Eastern Russian Plate and its Mineralogical and Geochemical Features

The long continental period in the East of the Russian plate (the upper Proterozoic – the middle Devonian) caused the formation of a weathering crust on the crystalline basement rocks. In pre-Devonian time, due to the washing-out and the subsequent processes of redeposition of substance, two types of weathering crust were formed: displaced and non-displaced. The widespread weathering crust of the crystalline basement of the East of the Russian plate is a unique object for studying the mineral formation processes of ancient weathering. Complex mineralogical and geochemical studies of the weathering crust are of practical value for the creation of a full picture of the development of the deep horizons of the earth crust and a forecast of mineral deposits.

CAMAM: A Miniature Laser Ablation Ionisation Mass Spectrometer and Microscope‐Camera System for In Situ Investigation of the Composition and Morphology of Extraterrestrial Materials

Performance studies of a microscope‐camera system (MCS) and a laser ablation/ionisation mass spectrometer (LIMS) instrument (referred to here as a laser mass spectrometer or LMS) are presented. These two instruments were designed independently for in situ analysis of solids on planetary surfaces and will be combined to a single miniature instrument suite for in situ chemical and morphological analysis of surface materials on planetary bodies. LMS can perform sensitive chemical (elemental, isotope and molecular) analyses with spatial resolution close to micrometre‐sized grains. It allows for studies with mass resolution (M/ΔM) up to 800 in ablation mode (elemental composition) and up to 1500 in desorption mode (molecular analysis). With an effective dynamic range of at least eight orders of magnitude, sensitive and quantitative measurements can be conducted of almost all elements and isotopes with a concentration larger than a few ppb atoms. Hence, in addition to the major element composition, which is important for the determination of mineralogical constituents of surface materials, trace elements can also be measured to provide information on mineral formation processes. Highly accurate isotope ratio measurements can be used to determine in situ geochronology of sample material and for investigations of various isotope fractionation processes. MCS can conduct optical imagery of mm‐sized objects at several wavelengths with micrometre spatial resolution for the characterisation of morphological surface details and to provide insight into surface mineralogy. Furthermore, MCS can help in the selection of sample surface areas for further mass spectrometric analysis of the chemical composition. Surface auto‐fluorescence measurements and images in polarised light are additional capabilities of the MCS, to identify either fluorescing minerals or organic materials, if present on the analysed surface, for further investigation by LMS. The results obtained by investigations of NIST reference materials, amino acid films and a natural graphite sample embedded in silicate rock are presented to illustrate the performance of the instruments and their potential to deliver chemical information for mineral and organic phases in their geological context.