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At least 469 records · Page 26Linked to original sources

Carbon sequestration via reaction with basaltic rocks: geochemical modeling and experimental results

Basaltic rocks are potential repositories for sequestering carbon dioxide (CO 2 ) because of their capacity for trapping CO 2 in carbonate minerals. We carried out a series of thermodynamic equilibrium models and high pressure experiments, reacting basalt with CO 2 -charged fluids over a range of conditions from 50 to 200 °C at 300 bar. Results indicate basalt has a high reactivity to CO 2 acidified brine. Carbon dioxide is taken up from solution at all temperatures from 50 to 200 °C, 300 bar, but the maximum extent and rate of reaction occurs at 100 °C, 300 bar. Reaction path simulations utilizing the geochemical modeling program CHILLER predicted an equilibrium carbonate alteration assemblage of calcite, magnesite, and siderite, but the only secondary carbonate identified in the experiments was a ferroan magnesite. The amount of uptake at 100 °C, 300 bar ranged from 8% by weight for a typical tholeite to 26% for a picrite. The actual amount of CO2 uptake and extent of rock alteration coincides directly with the magnesium content of the rock suggesting that overall reaction extent is controlled by bulk basalt Mg content. In terms of sequestering CO 2 , an average basaltic MgO content of 8% is equivalent to 2.6 × 10 8 metric ton CO 2 /km 3 basalt.

Geochimica et Cosmochimica Acta↗

Carbon cycling in the mantled karst of the Ozark Plateaus, central United States

The nature of carbon (C) cycling in the unsaturated zone where groundwater is in contact with abundant gas-filled voids is poorly understood. The objective of this study was to trace inorganic-C cycling in a karst landscape using stable-C isotopes, with emphasis on a shallow groundwater flow path through the soil, to an underlying cave, and to the spring outlet of a cave stream in the Ozark Plateaus of northwestern Arkansas. Carbon dioxide (CO 2 ) concentration and isotopic composition (δ 13 C-CO 2 ) in gas and dissolved inorganic carbon (DIC) concentration and isotopic composition (δ 13 C-DIC) in water were measured in samples collected from two suction-cup soil samplers above the cave, three sites in the cave, and at the spring outlet of the cave stream. Soil-gas CO 2 concentration (median 2,578 ppm) and δ 13 C-CO 2 (median − 21.5‰) were seasonally variable, reflecting the effects of surface temperature changes on soil-CO 2 production via respiration and organic-matter decomposition. Cave-air CO 2 (median 1,026 ppm) was sourced from the soil zone and the surface atmosphere, with seasonally changing proportions of each source controlled by surface temperature-driven air density gradients. Soil-DIC concentration (median 1.7 mg L − 1 ) was lower and soil-δ 13 C-DIC (median − 19.5‰) was lighter compared to the cave (median 23.3 mg L − 1 and − 14.3‰, respectively) because carbonate-bedrock dissolution provided an inorganic source of C to the cave. Carbon species in the soil had a unique, light stable-C isotopic signature compared to the cave. Discrimination of soil-C sources to karst groundwater was achieved, which is critical for developing hydrologic budgets using environmental tracers such as C.

Geoderma Regional↗

Organic petrography of Leonardian (Wolfcamp A) mudrocks and carbonates, Midland Basin, Texas: The fate of oil-prone sedimentary organic matter in the oil window

To better understand evolution of oil-prone sedimentary organic matter to petroleum and expulsion from source rock, we evaluated organic petrographic features of Leonardian Wolfcamp A repetitive siliceous and calcareous mudrock and fine-grained carbonate lithofacies cycles occurring in the R. Ricker #1 core from Reagan County, Midland Basin, Texas. The objectives of the petrographic investigation were to estimate thermal maturity, identify organic matter types and abundances, and identify the presence or absence of migrated hydrocarbons in organic-lean carbonate layers. An integrated analytical program included geochemical screening [total organic carbon (TOC) content by LECO, programmed pyrolysis by hydrocarbon analyzer with kinetics (HAWK) including analysis of solvent-extracted samples], X-ray diffraction mineralogy, organic petrography, scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) including correlative light and electron microscopy (CLEM), and micro-Fourier transform infrared spectroscopy (μ-FTIR) analyses of solid bitumen. The data indicate all samples are early to middle oil window thermal maturity with solid bitumen reflectance (BR o ) values of 0.55–0.86% and T max of 440–455 °C. Organic matter is predominantly solid bitumen (as identified by optical microscopy) in all lithofacies with minor contributions from inertinite. Solid bitumen abundance decreases from siliceous mudrock (TOC >3.0 wt%) to calcareous mudrock (TOC 1.0 to 3.0 wt%) to fine-grained carbonate (TOC <1.0 wt%) lithofacies. Interpretations of petrographic data suggest siliceous and calcareous mudrocks are source rock lithofacies and contain solid bitumen (with petroleum generation potential) that is residual (what remains) from conversion of an original Type II sedimentary organic matter. In turn, fine-grained carbonates are interpreted as reservoir lithofacies which contained little or no original oil-prone sedimentary organic matter and at present-day contain only a minor component of migrated solid petroleum sourced from adjacent siliceous and calcareous mudrock lithofacies. This work helps to document petroleum generation and migration processes, improve unconventional reservoir characterization and better define areas of oil window thermal maturity in an area critical to United States hydrocarbon production.

Texas↗

Lake carbonate-δ 18 records from the Yukon Territory, Canada: Little Ice Age moisture variability and patterns

A 1000-yr history of climate change in the central Yukon Territory, Canada, is inferred from sediment composition and isotope geochemistry from small, groundwater fed, Seven Mile Lake. Recent observations of lake-water &delta; 18 O, lake level, river discharge, and climate variations, suggest that changes in regional effective moisture (precipitation minus evaporation) are reflected by the lake&rsquo;s hydrologic balance. The observations indicate that the lake is currently 18 O-enriched by summer evaporation and that during years of increased precipitation, when groundwater inflow rates to the lake increase, lake-water &delta; 18 O values decrease. Past lake-water &delta; 18 O values are inferred from oxygen isotope ratios of fine-grained sedimentary endogenic carbonate. Variations in carbonate &delta; 18 O, supplemented by those in carbonate and organic &delta; 13 C, C/N ratios, and organic carbon, carbonate and biogenic silica accumulation rates, document changes in effective moisture at decadal time scales during the early Little Ice Age period to present. Results indicate that between &sim;AD 1000 and 1600, effective moisture was higher than today. A shift to more arid climate conditions occurred after &sim;AD 1650. The 19th and 20th centuries have been the driest of the past millennium. Temporal variations correspond with inferred shifts in summer evaporation from Marcella Lake &delta; 18 O, a similarly small, stratified, alkaline lake located &sim;250 km to the southwest, suggesting that the combined reconstructions accurately document the regional paleoclimate of the east-central interior. Comparison with regional glacial activity suggests differing regional moisture patterns during early and late Little Ice Age advances.

Yukon Territory↗

Late Holocene vegetation, climate, and land-use impacts on carbon dynamics in the Florida Everglades

Tropical and subtropical peatlands are considered a significant carbon sink. The Florida Everglades includes 6000-km 2 of peat-accumulating wetland; however, detailed carbon dynamics from different environments within the Everglades have not been extensively studied or compared. Here we present carbon accumulation rates from 13 cores and 4 different environments, including sawgrass ridges and sloughs, tree islands, and marl prairies, whose hydroperiods and vegetation communities differ. We find that the lowest rates of C accumulation occur in sloughs in the southern Everglades. The highest rates are found where hydroperiods are generally shorter, including near-tails of tree islands and drier ridges. Long-term average rates of 100 to >200 g C m &minus;2 yr &minus;1 are as high, and in some cases, higher than rates recorded from the tropics and 10&ndash;20 times higher than boreal averages. C accumulation rates were impacted by both the Medieval Climate Anomaly and the Little Ice Age, but the largest impacts to C accumulation rates over the Holocene record have been the anthropogenic changes associated with expansion of agriculture and construction of canals and levees to control movement of surface water. Water management practices in the 20th century have altered the natural hydroperiods and fire regimes of the Everglades. The Florida Everglades as a whole has acted as a significant carbon sink over the mid- to late-Holocene, but reduction of the spatial extent of the original wetland area, as well as the alteration of natural hydrology in the late 19th and 20th centuries, have significantly reduced the carbon sink capacity of this subtropical wetland.

Florida↗

Estimating burn severity and carbon emissions from a megafire in boreal forests of China

Wildfires, especially those of large size, worsen air quality and alter the carbon cycle through combustion of large quantities of biomass and release of carbon into the atmosphere. The Black Dragon fire, which occurred in 1987 in the boreal forests of China is among the top five of such megafires ever recorded in the world. With over 30 years of accumulation of data and availability of new greenhouse gas emission accounting methods, carbon emissions from this megafire can now be estimated with improved precision and greater spatial resolution. To do this, we combined field and remote sensing data to map four burn severity classes and calculated combustion efficiency in terms of the biomass immediately consumed in the fire. Results of the study showed that 1.30 million hectares burned and 52% of that area burned with high severity. The emitted carbon dioxide equivalents (CO2e), accounted for approximately 10% of total fossil fuel emissions from China in 1987, along with CO (2%–3% of annual anthropogenic CO emissions from China) and non-methane hydrocarbons (NMHC) contributing to the atmospheric pollutants. Our study provides an important basis for carbon emission estimation and understanding the impacts of megafires.

Science of the Total Environment↗

Soil carbon consequences of historic hydrologic impairment and recent restoration in coastal wetlands

Coastal wetlands provide key ecosystem services, including substantial long-term storage of atmospheric CO2 in soil organic carbon pools. This accumulation of soil organic matter is a vital component of elevation gain in coastal wetlands responding to sea-level rise. Anthropogenic activities that alter coastal wetland function through disruption of tidal exchange and wetland water levels are ubiquitous. This study assesses soil vertical accretion and organic carbon accretion across five coastal wetlands that experienced over a century of impounded hydrology, followed by restoration of tidal exchange 5 to 14 years prior to sampling. Nearby marshes that never experienced tidal impoundment served as controls with natural hydrology to assess the impact of impoundment and restoration. Dated soil cores indicate that elevation gain and carbon storage were suppressed 30–70 % during impoundment, accounting for the majority of elevation deficit between impacted and natural sites. Only one site had substantial subsidence, likely due to oxidation of soil organic matter. Vertical and carbon accretion gains were achieved at all restored sites, with carbon burial increasing from 96 ± 33 to 197 ± 64 g C m −2 y −1 . The site with subsidence was able to accrete at double the rate (13 ± 5.6 mm y −1 ) of the natural complement, due predominantly to organic matter accumulation rather than mineral deposition, indicating these ecosystems are capable of large dynamic responses to restoration when conditions are optimized for vegetation growth. Hydrologic restoration enhanced elevation resilience and climate benefits of these coastal wetlands.

Massachusetts↗

Radioisotope tracer studies of inorganic carbon and Ca in microbially derived CaCO3

Microbial calcification significantly impacts the cycling and deposition of inorganic carbon. This research employs 45 Ca and 14 C techniques as radioisotopic tracers to examine the role of cellular cycling of Ca 2+ and inorganic carbon in CaCO 3 precipitation by the unicellular green alga Nannochloris atomus. Implications of the effects of these physiological aspects on CaCO 3 precipitation and the effects of microbial calcification on CaCO 3 δ 13 C ratios are discussed. Results from pulse/chase experiments indicate that intracellular Ca 2+ is incorporated into extracellular CaCO 3 . Intracellular inorganic carbon leaks from cells within 10 to 12 s after injection of unlabelled NaHCO 3 , providing a source of inorganic carbon for extracellular CaCO 3 . Cellular expulsion of calcium plays a key role in increasing the CaCO 3 saturation state at the site of calcification. The δ 13 C ratios of microbial carbonates may vary depending on the amount of photorespiratory CO 2 incorporated.

Geochimica et Cosmochimica Acta↗

Tracing and quantifying magmatic carbon discharge in cold groundwaters: Lessons learned from Mammoth Mountain, USA

A major campaign to quantify the magmatic carbon discharge in cold groundwaters around Mammoth Mountain volcano in eastern California was carried out from 1996 to 1999. The total water flow from all sampled cold springs was ??? 1.8 ?? 107 m3/yr draining an area that receives an estimated 2.5 ?? 107 m3/yr of recharge, suggesting that sample coverage of the groundwater system was essentially complete. Some of the waters contain magmatic helium with 3He/4He ratios as high as 4.5 times the atmospheric ratio, and a magmatic component in the dissolved inorganic carbon (DIC) can be identified in virtually every feature sampled. Many waters have a 14C of 0-5 pmC, a ??13C near -5???, and contain high concentrations (20-50 mmol/1) of CO2(aq); but are otherwise dilute (specific conductance = 100-300 ??S/cm) with low pH values between 5 and 6. Such waters have previously escaped notice at Mammoth Mountain, and possibly at many other volcanoes, because CO2 is rapidly lost to the air as the water flows away from the springs, leaving neutral pH waters containing only 1-3 mmol/1 HCO-3. The total discharge of magmatic carbon in the cold groundwater system at Mammoth Mountain is ~ 20 000 t/yr (as CO2), ranging seasonally from about 30 to 90 t/day. Several types of evidence show that this high discharge of magmatic DIC arose in part because of shallow dike intrusion in 1989, but also demonstrate that a long-term discharge possibly half this magnitude (~ 10 000 t/yr) predated that intrusion. To sustain a 10 000 t/yr DIC discharge would require a magma intrusion rate of 0.057 km3 per century, assuming complete degassing of magma with 0.65 wt% CO2 and a density of 2.7 t/m3. The geochemical data also identify a small ( < 1 t/day) discharge of magmatic DIC that can be traced to the Inyo Domes area north of Mammoth Mountain and outside the associated Long Valley caldera. This research, along with recent studies at Lassen Peak and other western USA volcanoes, suggests that the amount of magmatic carbon in cold groundwaters is important to constraining rates of intrusion and edifice weathering at individual volcanoes and may even represent a significant fraction of the global carbon discharge from volcanoes. ?? 2002 Elsevier Science B.V. All rights reserved.

Journal of Volcanology and Geothermal Research↗

Preparation and evaluation of coal-derived activated carbons for removal of mercury vapor from simulated coal combustion flue fases

Coal-derived activated carbons (CDACs) were tested for their suitability in removing trace amounts of vapor-phase mercury from simulated flue gases generated by coal combustion. CDACs were prepared in bench-scale and pilot-scale fluidized-bed reactors with a three-step process, including coal preoxidation, carbonization, and then steam activation. CDACs from high-organicsulfur Illinois coals had a greater equilibrium Hg0 adsorption capacity than activated carbons prepared from a low-organic-sulfur Illinois coal. When a low-organic-sulfur CDAC was impregnated with elemental sulfur at 600 ??C, its equilibrium Hg0 adsorption capacity was comparable to the adsorption capacity of the activated carbon prepared from the high-organicsulfur coal. X-ray diffraction and sulfur K-edge X-ray absorption near-edge structure examinations showed that the sulfur in the CDACs was mainly in organic forms. These results suggested that a portion of the inherent organic sulfur in the starting coal, which remained in the CDACs, played an important role in adsorption of Hg0. Besides organic sulfur, the BET surface area and micropore area of the CDACs also influenced Hg0 adsorption capacity. The HgCl2 adsorption capacity was not as dependent on the surface area and concentration of sulfur in the CDACs as was adsorption of Hg0. The properties and mercury adsorption capacities of the CDACs were compared with those obtained for commercial Darco FGD carbon.

Energy and Fuels↗

Modeling soil thermal and carbon dynamics of a fire chronosequence in interior Alaska

In this study, the dynamics of soil thermal, hydrologic, and ecosystem processes were coupled to project how the carbon budgets of boreal forests will respond to changes in atmospheric CO 2 , climate, and fire disturbance. The ability of the model to simulate gross primary production and ecosystem respiration was verified for a mature black spruce ecosystem in Canada, the age-dependent pattern of the simulated vegetation carbon was verified with inventory data on aboveground growth of Alaskan black spruce forests, and the model was applied to a postfire chronosequence in interior Alaska. The comparison between the simulated soil temperature and field-based estimates during the growing season (May to September) of 1997 revealed that the model was able to accurately simulate monthly temperatures at 10 cm ( R > 0.93) for control and burned stands of the fire chronosequence. Similarly, the simulated and field-based estimates of soil respiration for control and burned stands were correlated ( R = 0.84 and 0.74 for control and burned stands, respectively). The simulated and observed decadal to century-scale dynamics of soil temperature and carbon dynamics, which are represented by mean monthly values of these variables during the growing season, were correlated among stands ( R = 0.93 and 0.71 for soil temperature at 20- and 10-cm depths, R = 0.95 and 0.91 for soil respiration and soil carbon, respectively). Sensitivity analyses indicate that along with differences in fire and climate history a number of other factors influence the response of carbon dynamics to fire disturbance. These factors include nitrogen fixation, the growth of moss, changes in the depth of the organic layer, soil drainage, and fire severity.

Alaska↗

Climatically driven loss of calcium in steppe soil as a sink for atmospheric carbon

During the last several thousand years the semi-arid, cold climate of the Russian steppe formed highly fertile soils rich in organic carbon and calcium (classified as Chernozems in the Russian system). Analysis of archived soil samples collected in Kemannaya Steppe Preserve in 1920, 1947, 1970, and fresh samples collected in 1998 indicated that the native steppe Chernozems, however, lost 17-28 kg m-2 of calcium in the form of carbonates in 1970-1998. Here we demonstrate that the loss of calcium was caused by fundamental shift in the steppe hydrologic balance. Previously unleached soils where precipitation was less than potential evapotranspiration are now being leached due to increased precipitation and, possibly, due to decreased actual evapotranspiration. Because this region receives low levels of acidic deposition, the dissolution of carbonates involves the consumption of atmospheric CO2. Our estimates indicate that this climatically driven terrestrial sink of atmospheric CO2 is ???2.1-7.4 g C m-2 a-1. In addition to the net sink of atmospheric carbon, leaching of pedogenic carbonates significantly amplified seasonal amplitude of CO2 exchange between atmosphere and steppe soil. Copyright 2008 by the American Geophysical Union.

Global Biogeochemical Cycles↗

Upscaling carbon fluxes over the Great Plains grasslands: Sinks and sources

Previous studies suggested that the grasslands may be carbon sinks or near equilibrium, and they often shift between carbon sources in drought years and carbon sinks in other years. It is important to understand the responses of net ecosystem production (NEP) to various climatic conditions across the U.S. Great Plains grasslands. Based on 15 grassland flux towers, we developed a piecewise regression model and mapped the grassland NEP at 250 m spatial resolution over the Great Plains from 2000 to 2008. The results showed that the Great Plains was a net sink with an averaged annual NEP of 24 ± 14 g C m −2 yr −1 , ranging from a low value of 0.3 g C m −2 yr −1 in 2002 to a high value of 47.7 g C m −2 yr −1 in 2005. The regional averaged NEP for the entire Great Plains grasslands was estimated to be 336 Tg C yr −1 from 2000 to 2008. In the 9 year period including 4 dry years, the annual NEP was very variable in both space and time. It appeared that the carbon gains for the Great Plains were more sensitive to droughts in the west than the east. The droughts in 2000, 2002, 2006, and 2008 resulted in increased carbon losses over drought-affected areas, and the Great Plains grasslands turned into a relatively low sink with NEP values of 15.8, 0.3, 20.1, and 10.2 g C m −2 yr −1 for the 4 years, respectively.

Journal of Geophysical Research: Biogeosciences↗

Organic carbon burial rates in mangrove sediments: strengthening the global budget

Mangrove wetlands exist in the transition zone between terrestrial and marine environments and as such were historically overlooked in discussions of terrestrial and marine carbon cycling. In recent decades, mangroves have increasingly been credited with producing and burying large quantities of organic carbon (OC). The amount of available data regarding OC burial in mangrove soils has more than doubled since the last primary literature review (2003). This includes data from some of the largest, most developed mangrove forests in the world, providing an opportunity to strengthen the global estimate. First-time representation is now included for mangroves in Brazil, Colombia, Malaysia, Indonesia, China, Japan, Vietnam, and Thailand, along with additional data from Mexico and the United States. Our objective is to recalculate the centennial-scale burial rate of OC at both the local and global scales. Quantification of this rate enables better understanding of the current carbon sink capacity of mangroves as well as helps to quantify and/or validate the other aspects of the mangrove carbon budget such as import, export, and remineralization. Statistical analysis of the data supports use of the geometric mean as the most reliable central tendency measurement. Our estimate is that mangrove systems bury 163 (+40; -31) g OC m -2 yr -1 (95% C.I.). Globally, the 95% confidence interval for the annual burial rate is 26.1 (+6.3; -5.1) Tg OC. This equates to a burial fraction that is 42% larger than that of the most recent mangrove carbon budget (2008), and represents 10&ndash;15% of estimated annual mangrove production. This global rate supports previous conclusions that, on a centennial time scale, 8&ndash;15% of all OC burial in marine settings occurs in mangrove systems.

Global Biogeochemical Cycles↗

Predicted vulnerability of carbon in permafrost peatlands With future climate change and permafrost thaw in western Canada

Climate warming in high-latitude regions is thawing carbon-rich permafrost soils, which can release carbon to the atmosphere and enhance climate warming. Using a coupled model of long-term peatland dynamics (Holocene Peat Model, HPM-Arctic), we quantify the potential loss of carbon with future climate warming for six sites with differing climates and permafrost histories in Northwestern Canada. We compared the net carbon balance at 2100 CE resulting from new productivity and the decomposition of active layer and newly thawed permafrost peats under RCP8.5 as a high-end constraint. Modeled net carbon losses ranged from −3.0 kg C m −2 (net loss) to +0.1 kg C m −2 (net gain) between 2015 and 2100. Losses of newly thawed permafrost peat comprised 0.2%–25% (median: 1.6%) of “old” C loss, which were related to the residence time of peat in the active layer before being incorporated into the permafrost, peat temperature, and presence of permafrost. The largest C loss was from the permafrost-free site, not from permafrost sites. C losses were greatest from depths of 0.2–1.0 m. New C added to the profile through net primary productivity between 2015 and 2100 offset ∼40% to >100% of old C losses across the sites. Differences between modeled active layer deepening and flooding following permafrost thaw resulted in very small differences in net C loss by 2100, illustrating the important role of present-day conditions and permafrost aggradation history in controlling net C loss.

western Canada↗

Springtime formation of laminated soil carbonate rinds and changes in fluvial terrace soils on orbital timescales at Rio Mesa, Utah, USA

Laminated soil carbonate rinds are a Quaternary paleoclimate archive whose isotope composition is linked to soil formation conditions. At Rio Mesa, Utah (USA), we investigated the fidelity of rind records in a river terrace setting by determining the seasonal timing of rind formation and testing for inter-record replication. We infer soil carbonate formed in the spring season, contrasting with our prior inference of summer formation at Teasdale, Utah, ≈200 km distant. This apparent discrepancy occurs because of differences in the timing of the largest annual infiltration (spring vs. summer). At Rio Mesa, modern soil data show that soil carbonate δ 13 C would have high values (−2 to 2‰ VPDB) regardless of seasonal activity of C 3 versus C 4 plants because respiration rate is a strong control. We accordingly suggest reassessment of published records interpreting soil carbonate δ 13 C only via C 3 versus C 4 plant abundance. Three rind δ 13 C and δ 18 O records generally replicated. Intriguingly, rind δ 13 C may inversely correlate with summer insolation, evidence for global-scale influence on soils. Rind δ 18 O is not as clearly correlated with published western USA paleoclimate records, potentially due to regional differences in climate and because rinds record soil-specific processes. Our results support the fidelity of the soil carbonate rind paleoarchive and suggest that because rind formation seasonality is intimately tied to infiltration seasonality, spatial transects of rind records might be used to delineate boundaries between areas dominated by spring and summer infiltration, permitting reconstruction of the geographic extent of large-scale hydrologic phenomena such as the North American Monsoon.

Utah↗

Evidence of mineral alteration in a salt marsh subterranean estuary: Implications for carbon and trace element cycling

Subterranean estuaries (STE) in salt marshes are biogeochemically active zones where interactions between terrestrial groundwater and seawater drive complex cycling of carbon and trace elements, influenced by mineral dissolution. These systems, characterized by fine-grained organic-rich peat overlying permeable coastal aquifers, play a crucial role as a blue carbon sink, yet their geochemical dynamics remain poorly understood. We investigated dissolved trace elements, carbon, silica, and radium isotopes in a salt marsh STE (Sage Lot Pond, Waquoit Bay, MA) over seasonal and annual cycles. Our results reveal that groundwater and estuarine water circulation through marsh peat and aquifer sediments leads to enrichments of dissolved organic and inorganic carbon (DOC and DIC), Si, Ba, and Mn, with variable source/sink behavior of Fe and net removal of U. Submarine groundwater discharge dominated Ba fluxes, whereas pore water drainage from marsh peat acted as the main sink for U and source of Si. Fe cycling was variable, with terrestrial Fe largely removed as groundwater passed through the STE, consistent with Fe-sulfide and amorphous phase formation. Radium isotope ratios identified two distinct subsurface flow pathways, influenced by metal-oxide cycling and organic matter breakdown. Si production was decoupled from DIC, suggesting Si originates from mineral alteration, whereas DIC results from both mineral weathering and microbial respiration. Silicate mineral alteration, coupled with marsh pore water drainage, accounts for up to 16% of annual DIC exports (66 g C m −2 y −1 ), highlighting the importance of STEs in coastal carbon and trace element cycling, especially as marshes face environmental change.

Massachusetts↗

A fundamental role of carbonate–sulfate melts in the formation of iron oxide–apatite deposits

Genetic models for iron oxide–apatite deposits are controversial and span a spectrum from orthomagmatic to hydrothermal endmembers. This lack of consensus is rooted in uncertainties as to the nature and origin of ore-forming fluids in these systems. Here, we present a fluid-inclusion study of mineralizing fluids at two iron oxide–apatite deposits (Buena Vista, Nevada and Iron Springs, Utah). We found that the inclusions in both systems comprise both aqueous brine and ubiquitous iron-rich carbonate–sulfate melts. These melts were found throughout the paragenesis of both deposits and show a tremendous capacity to transport ferric iron. Hence, we argue that orthomagmatic fluids played a role in mineralization at both Buena Vista and Iron Springs, and that the main ore-forming fluid was an iron-rich carbonate–sulfate melt formed by the assimilation and anatexis of evaporite-bearing carbonate rocks. The geological conditions that give rise to carbonate–sulfate melts are also a common feature of other classic iron oxide–apatite systems worldwide. Hence, we argue that the process of assimilation, anatexis and immiscibility of carbonate–sulfate melts is fundamental to iron oxide–apatite formation and provides a common link between iron oxide–apatite systems in different geological settings.

Nature Geoscience↗