Progressive veining during peridotite carbonation: insights from listvenites in Hole BT1B, Samail ophiolite (Oman)

The reaction of serpentinized peridotites with CO2-bearing fluids to listvenite (quartz-carbonate rocks) requires massive fluid flux and significant permeability despite increase in solid volume. Listvenite and serpentinite samples from Hole BT1B of the Oman Drilling Project help to understand mechanisms and feedbacks during vein formation in this process. Samples analyzed in this study contain abundant magnesite veins in closely spaced, parallel sets and younger quartz-rich veins. Cross-cutting relationships suggest that antitaxial, zoned carbonate veins with elongated grains growing from a median zone towards the wall rock are among the earliest structures to form during carbonation of serpentinite. Their bisymmetric chemical zoning of variable Ca and Fe contents, a systematic distribution of SiO2 and Fe-oxide inclusions in these zones, and cross-cutting relations with Fe-oxides and Cr-spinel indicate that they record progress of reaction fronts during replacement of serpentine by carbonate in addition to dilatant vein growth. Euhedral terminations and growth textures of carbonate vein fill together with local dolomite precipitation and voids along the vein – wall rock interface suggest that these antitaxial veins acted as preferred fluid pathways allowing infiltration of CO2-rich fluids necessary for carbonation to progress. Fluid flow was probably further enabled by external tectonic stress, as indicated by closely spaced sets of subparallel carbonate veins. Despite widespread subsequent quartz mineralization in the rock matrix and veins, which most likely caused a reduction in the permeability network, carbonation proceeded to completion in listvenite horizons.

Dolomite genesis in bioturbated marine zones of an early-middle Miocene coastal mud volcano outcrop (Kuwait)

The origin of spheroidal dolomitized burrow from Al-Subiya sabkha in Kuwait was previously described as enigmatic as no evidence of precursor calcium carbonate was found in the siliciclastic sediment. An assumption for the genesis of spheroidal dolomite from the same area was attributed to hydrocarbon seepage but no evidence was provided. Here, we investigated a recently discovered early-middle Miocene coastal mud volcano outcrop in Al-Subiya sabkha where dolomitized burrows and spheroidal dolomite are found in bioturbated marine zones, and associated with traces of salt. Conversely, the continental zone lacks bioturbation features, dolomite and traces of salt, which together contrast with bioturbated rich marine zones. Geochemical signatures of Rare Earth Elements + Yttrium show a true positive Ce anomaly (Ce/Ce* > 1.2) and positive Eu/Eu* anomaly of spheroidal dolomite indicating strictly anoxic conditions, and sulphate reduction to sulphide, respectively. Our results are suggestive of a relationship between dolomite formation and interdependent events of hydrocarbon seepage, flux of hypersaline seawater, bioturbation, and fluid flow in the marine zones of the mud volcano. The bioturbation activity of crustaceans introduced channels/burrows in the sediment–water interface allowing for the mixing of seeped pressurized hydrocarbon-charged fluids, and evaporitic seawater. In the irrigated channels/burrows, the seeped pressurized hydrocarbon-charged fluids were oxidized via microbial consortia of methanotrophic archaea and sulphate-reducing bacteria resulting in elevated alkalinity and saturation index with respect to dolomite, thus providing the preferential geochemical microenvironment for dolomite precipitation in the bioturbated sediment.

From poorly-ordered precursors to crystals: Factors contributing to spherulitic growth of dolomite

<p>Dolomite is one of the most abundant carbonate minerals in the geological record, yet it barely forms in the present. The contrast in the abundance of dolomite between geological and modern records combined with the impossibility of synthesizing stoichiometric dolomite in the laboratory at ambient conditions are known as the 'dolomite problem'. This enigma has been in the scope of research for decades, trying to understand dolomite formation, mechanisms and the contributing factors. Dolomite is known to form via two abiotic mechanisms; through (1) dolomitization or (2) dolomite cementation. Also, the contribution of microorganisms can result in biotic dolomite crystallization. The mechanisms of dolomite formation at the molecular and nanoscale in biotic and abiotic environments are relatively well-described, but we still struggle to develop a unified model of dolomite formation in modern and ancient settings. In this contribution, we summarize the development of research related to the dolomite formation processes and in particular the direct dolomite precipitation via spherulitic growth of proto-dolomite.</p>

Study on Environmental Factors of Fluorine in Chagan Lake Catchment, Northeast China

The Chagan Lake Catchment is located in the midwest of Songnen Plain, which is a typical high fluoride groundwater area. High fluoride water has an important impact on the economic development and ecosystem stability of Chagan Lake. In this study, the spatial distribution characteristics and influencing factors of fluorine in Chagan Lake Catchment are discussed by using hydrochemistry and mathematical statistical analysis. The groundwater in the study area was characterized as Na+-rich and Ca2+-poor, with a high pH value and high HCO3– content. The average concentration of F– was 3.02 mg/L, which was the highest in Qian’an County. The dissolution of fluorine-containing minerals and the desorption of F– in soil provided the source of F– in groundwater, while calcite and dolomite precipitation, cation exchange, and evaporation concentration provided favorable conditions for F– dissolving, migration, and enrichment in water. In addition, the concentration of F– in surface water was 4.56 mg/L, and the highest concentration was found in Hongzi Pool and Hua’ao Pool. The elevated concentrations of F– in both surface water and groundwater in the study were affected by human factors, such as rice planting and water conservancy project construction.

Modern dolomite formation caused by seasonal cycling of oxygenic phototrophs and anoxygenic phototrophs in a hypersaline sabkha

The “Dolomite Problem” has been a controversy for over a century, owing to massive assemblages of low-temperature dolomite in ancient rocks with little dolomite forming today despite favorable geochemical conditions. Experiments show that microbes and their exopolymeric substances (EPS) nucleate dolomite. However, factors controlling ancient abundances of dolomite can still not be explained. To decode the enigma of ancient dolomite, we examined a modern dolomite forming environment, and found that a cyclic shift in microbial community between cyanobacteria and anoxygenic phototrophs creates EPS suited to dolomite precipitation. Specifically, EPS show an increased concentration of carboxylic functional groups as microbial composition cycles from cyanobacterial to anoxygenic phototroph driven communities at low-and high- salinity, respectively. Comparing these results to other low-T forming environments suggests that large turnover of organic material under anoxic conditions is an important driver of the process. Consequently, the shift in atmospheric oxygen throughout Earth’s history may explain important aspects of “The Dolomite Problem”. Our results provide new context for the interpretation of dolomite throughout Earth’s history.

Use of Calcined Dolomite as Chemical Precipitant in the Simultaneous Removal of Ammonium and Phosphate from Synthetic Wastewater and from Agricultural Sludge

Phosphorus as phosphate and nitrogen as ammonium or nitrate are the main nutrients in wastewaters and agricultural sludges. They runoff easily to waterways and cause eutrophication in water bodies. However, ammonium and phosphate could be precipitated simultaneously and used as recycled nutrients. In this research, dolomite calcined at 650 °C, 750 °C, or 950 °C and commercial MgO were used as precipitants in simultaneous phosphate and ammonium removal from synthetic (NH4)2HPO4 solution and agricultural sludge. Calcination at 750 °C was the preferred option as dolomite was decomposed to MgO and CaCO3 for optimal struvite precipitation. Molar ratios of 1.1–1.6:1–2:2 (Mg:P:N) were employed in the experiments. Very robust ammonium removal was obtained with MgO (57%), dolomite 650 °C and dolomite 750 °C (75%). MgO removed almost all phosphate, while dolomite 650 °C removed 65%, and dolomite 750 °C removed 60% (70% from agricultural sludge). Some part of the phosphate was adsorbed, most likely by CaCO3, during dolomite precipitation. Struvite was the only identified reaction product in all samples after 24 h of precipitation. Calcined dolomite had great potential in ammonium and phosphate precipitation from both synthetic waters and agricultural sludges and the precipitates could be used as recycled fertilizers.