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At least 325 records · Page 18Linked to original sources
USGS2020

Changes in ecosystem nitrogen and carbon allocation with black mangrove (Avicennia germinans) encroachment into Spartina alterniflora salt marsh

Increases in temperature are expected to facilitate encroachment of tropical mangrove forests into temperate salt marshes, yet the effects on ecosystem services are understudied. Our work was conducted along a mangrove expansion front in Louisiana (USA), an area where coastal wetlands are in rapid decline due to compounding factors, including reduced sediment supply, rising sea level, and subsidence. Marsh and mangrove ecosystems are each known for their ability to adjust to sea-level rise and support numerous ecosystem services, but there are some differences in the societal benefits they provide. Here, we compare carbon and nitrogen stocks and relate these findings to the expected effects of mangrove encroachment on nitrogen filtration and carbon sequestration in coastal wetlands. We specifically evaluate the implications of black mangrove ( Avicennia germinans ) encroachment into Spartina alterniflora -dominated salt marsh. Our results indicate that black mangrove encroachment will lead to increased aboveground carbon and nitrogen stocks. However, we found no differences in belowground (that is, root and sediment) nitrogen or carbon stocks between marshes and mangroves. Thus, the shift from marsh to mangrove may provide decadal-scale increases in aboveground nitrogen and carbon sequestration, but belowground nitrogen and carbon sequestration (that is, carbon burial) may not be affected. We measured lower pore water nitrogen content beneath growing mangroves, which we postulate may be due to greater nitrogen uptake and storage in mangrove aboveground compartments compared to marshes. However, further studies are needed to better characterize the implications of mangrove encroachment on nitrogen cycling, storage, and export to the coastal ocean.

Louisiana↗
USGS2011

Calcium carbonate nucleation in an alkaline lake surface water, Pyramid Lake, Nevada, USA

Calcium concentration and calcite supersaturation (Ω) needed for calcium carbonate nucleation and crystal growth in Pyramid Lake (PL) surface water were determined during August of 1997, 2000, and 2001. PL surface water has Ω values of 10-16. Notwithstanding high Ω, calcium carbonate growth did not occur on aragonite single crystals suspended PL surface water for several months. However, calcium solution addition to PL surface-water samples caused reproducible calcium carbonate mineral nucleation and crystal growth. Mean PL surface-water calcium concentration at nucleation was 2.33 mM ( n = 10), a value about nine times higher than the ambient PL surface-water calcium concentration (0.26 mM); mean Ω at nucleation (109 with a standard deviation of 8) is about eight times the PL surface-water Ω. Calcium concentration and Ω regulated the calcium carbonate formation in PL nucleation experiments and surface water. Unfiltered samples nucleated at lower Ω than filtered samples. Calcium concentration and Ω at nucleation for experiments in the presence of added particles were within one standard deviation of the mean for all samples. Calcium carbonate formation rates followed a simple rate expression of the form, rate (mM/min) = A (Ω) + B . The best fit rate equation "Rate (Δ mM/Δ min) = -0.0026 Ω + 0.0175 ( r = 0.904, n = 10)" was statistically significant at greater than the 0.01 confidence level and gives, after rearrangement, Ω at zero rate of 6.7. Nucleation in PL surface water and morphology of calcium carbonate particles formed in PL nucleation experiments and in PL surface-water samples suggest crystal growth inhibition by multiple substances present in PL surface water mediates PL calcium carbonate formation, but there is insufficient information to determine the chemical nature of all inhibitors.

Nevada↗
USGS2020

Carbon sources in the sediments of a restoring vs. historically unaltered salt marsh

Salt marshes provide the important ecosystem service of carbon storage in their sediments; however, little is known about the sources of such carbon and whether they differ between historically unaltered and restoring systems. In this study, stable isotope analysis was used to quantify carbon sources in a restoring, sparsely vegetated marsh (Restoring) and an adjacent, historically unaltered marsh (Reference) in the Nisqually River Delta (NRD) of Washington, USA. Three sediment cores were collected at “Inland” and “Seaward” locations at both marshes ~ 6 years after restoration. Benthic diatoms, C3 plants, C4 plants, and particulate organic matter (POM) were collected throughout the NRD. δ 13 C and δ 15 N values of sources and sediments were used in a Bayesian stable isotope mixing model to determine the contribution of each carbon source to the sediments of both marshes. Autochthonous marsh C3 plants contributed 73 ± 10% (98 g C m −2 year −1 ) and 89 ± 11% (119 g C m −2 year −1 ) to Reference-Inland and Reference-Seaward sediment carbon sinks, respectively. In contrast, the sediment carbon sink at the Restoring Marsh received a broad assortment of predominantly allochthonous materials, which varied in relative contribution based on source distance and abundance. Marsh POM contributed the most to Restoring-Seaward (42 ± 34%) (69 g C m −2 year −1 ) followed by Riverine POM at Restoring-Inland (32 ± 41%) (52 g C m −2 year −1 ). Overall, this study demonstrates that largely unvegetated, restoring marshes can accumulate carbon by relying predominantly on allochthonous material, which comes mainly from the most abundant and closest estuarine sources. ces.

Washington↗
USGS2022

Can coastal habitats rise to the challenge? Resilience of estuarine habitats, carbon accumulation, and economic value to sea-level rise in a Puget Sound estuary

Sea-level rise (SLR) and obstructions to sediment delivery pose challenges to the persistence of estuarine habitats and the ecosystem services they provide. Restoration actions and sediment management strategies may help mitigate such challenges by encouraging the vertical accretion of sediment in and horizontal migration of tidal forests and marshes. We used a process-based soil accretion model (Coastal Wetland Equilibrium Model) combined with a habitat classification model (MOSAICS) to estimate the effects of SLR, suspended sediment, and inland habitat migration on estuarine habitats, soil carbon accumulation, and economic value of climate change mitigation of carbon accumulation (social cost of carbon dioxide) in a macrotidal estuary in the northwest USA over 100 years (2011 to 2110). Under present-day sediment levels, we projected that after 100 years, most high salt marsh would remain with < 100 cm SLR, but substantial area converted to transitional (low) salt marsh and mudflat with ≥ 100 cm SLR. Increasing sediment availability increased the projected resilience of transitional salt marsh to SLR but did not prevent declines in high marsh area. Projected total carbon accumulation plateaued or declined with ≥ 100 cm SLR, yet the economic value of carbon accumulation continued to rise over time, suggesting that the value of this ecosystem service was resilient to SLR. Doubling or tripling sediment availability increased projected carbon accumulation up to 7.69 and 14.2 kg m −2 and increased total economic value up to $373,000 and $710,000, respectively. Allowing marsh migration supported conversion of upland to freshwater marsh, with slight increases in carbon accumulation. These results inform climate adaptation planning for wetland managers seeking to understand the resilience of estuarine habitats and ecosystem services to SLR under multiple management strategies.

Washington↗
USGS2013

A long-term comparison of carbon sequestration rates in impounded and naturally tidal freshwater marshes along the lower Waccamaw River, South Carolina

Carbon storage was compared between impounded and naturally tidal freshwater marshes along the Lower Waccamaw River in South Carolina, USA. Soil cores were collected in (1) naturally tidal, (2) moist soil (impounded, seasonally drained since ~1970), and (3) deeply flooded “treatments” (impounded, flooded to ~90 cm since ~2002). Cores were analyzed for % organic carbon, % total carbon, bulk density, and 210 Pb and 137 Cs for dating purposes. Carbon sequestration rates ranged from 25 to 200 g C m −2 yr −1 (moist soil), 80–435 g C m −2 yr −1 (naturally tidal), and 100–250 g C m −2 yr −1 (deeply flooded). The moist soil and naturally tidal treatments were compared over a period of 40 years. The naturally tidal treatment had significantly higher carbon storage (mean = 219 g C m −2 yr −1 vs. mean = 91 g C m −2 yr −1 ) and four times the vertical accretion rate (mean = 0.84 cm yr −1 vs. mean = 0.21 cm yr −1 ) of the moist soil treatment. The results strongly suggest that the long drainage period in moist soil management limits carbon storage over time. Managers across the National Wildlife Refuge system have an opportunity to increase carbon storage by minimizing drainage in impoundments as much as practicable.

South Carolina↗
USGS1984

Origin of epigenetic calcite in coal from Antarctica and Ohio based on isotope compositions of oxygen, carbon and strontium

Isotopic compositions of oxygen, carbon and strontium of calcite cleats in coal seams of southern Victoria Land, Antarctica, and Tuscarawas County, Ohio, contain a record of the conditions a the time of their formation. The Antarctic calcites (?? 18O(SMOW) = +9.14 to +11.82%0) were deposited from waters enriched in 16O whose isotopic composition was consistent with that of meteoric precipitation at low temperature and high latitude. The carbon of the calcite cleats (?? 13C(PDB) = -15.6 to -16.9%0) was derived in part from the coal (?? 13C(PDB) = -23.5 to -26.7%0) as carbon dioxide and by oxidation of methane or other hydrocarbon gases. The strontium ( 87Sr 86Sr = 0.71318-0.72392) originated primarily from altered feldspar grains in the sandstones of the Beacon Supergroup. Calcite cleats in the Kittaning No. 6 coal seam of Ohio (?? 18O(SMOW) = +26.04 to +27.79%0) were deposited from waters that had previously exchanged oxygen, possibly with marine carbonate at depth. The carbon (?? 13C(PDB) = 0.9 to +2.4%0) is enriched in 13C even though that cleats were deposited in coal that is highly enriched in 12C and apparently originated from marine carbonates. Strontium in the cleats ( Sr 87 0.71182-0.71260) is not of marine origin but contains varying amounts of radiogenic 87Sr presumably derived from detrital Rb-bearing minerals in the adjacent sedimentary rocks. The results of this study suggest that calcite cleats in coal of southern Victoria Land, Antarctica, were deposited after the start of glaciation in Cenozoic time and that those in Ohio precipitated from formation waters derived from the underlying marine carbonate rocks, probably in the recent geologic past. ?? 1984.

Chemical Geology↗
USGS1986

Carbon isotope systematics of a mantle "hotspot": A comparison of Loihi Seamount and MORB glasses

The carbon isotope geochemistry of glasses from Loihi Seamount has been compared with that of MORB glasses. Stepped heating shows two carbon components in both sample suites: (1) isotopically light carbon ( avg. δ 13 C = −26.3‰ ) released < 600°C, ascribed to surficial contamination, and (2) isotopically heavy carbon released > 600°C, regarded as indigenous. The high-temperature component in MORB samples varied from 52 to 169 ppm C, average δ 13 C = −6.6‰ , consistent with previous studies (overall MORD average δ 13 C = −6.4 ± 0.9‰ ), and new results for Indian Ocean glasses are similar to Atlantic and Pacific Ocean samples. Carbon release profiles produced by stepped heating may be typical of locality, but there are no significant differences in δ 13 C values between MORB samples from different areas. Lower yields (17–110 ppm C) correlated with depth in the Loihi samples suggest that they are partially degassed. This degassing has not affected δ 13 C values significantly (avg. −5.8‰). Loihi tholeiites have higher δ 13 C (avg. −5.6‰) than the alkali basalts (avg. −7.1‰). Carbon abundances correlate well with He concentration data. Comparison of the δ 13 C values with trace element and He, Sr, Nd, and Pb isotope data from the literature suggests that the Loihi samples with highest δ 13 C have high 3 He/ 4 He and possibly the least depleted 143 Nd/ 144 Nd and 87 Sr/ 86 Sr. The carbon isotope data are consistent with previous models for Loihi involving several mantle sources, lithospheric contamination, and mixing. The slightly higher δ 13 C of Loihi tholeiites suggests that the undegassed “plume” component manifested by high 3 He/ 4 He values might have δ 13 C about 1‰ higher than the MORB average.

Earth and Planetary Science Letters↗
USGS1992

Sulfur, carbon, and oxygen isotope variations in submarine hydrothermal deposits of Guaymas Basin, Gulf of California, USA

Sulfur, carbon, and oxygen isotope values were measured in sulfide, sulfate, and carbonate from hydrothermal chimney, spire, and mound samples in the southern trough of Guaymas Basin, Gulf of California, USA. δ 34 S values of sulfides range from −3.7 to 4.5%. and indicate that sulfur originated from several sources: 1. (1) dissolution of 0‰ sulfide contained within basaltic rocks, 2. (2) thermal reduction of seawater sulfate during sediment alteration reactions in feeder zones to give sulfide with positive δ 34 S , and 3. (3) entrainment or leaching of isotopically light (negative- δ 34 S ) bacteriogenic sulfide from sediments underlying the deposits. δ 34 S of barite and anhydrite indicate sulfur derivation mainly from unfractionated seawater sulfate, although some samples show evidence of sulfate reduction and sulfide oxidation reactions during mixing within chimneys. Oxygen isotope temperatures calculated for chimney calcites are in reasonable agreement with measured vent fluid temperatures and fluid inclusion trapping temperatures. Hydrothermal fluids that formed calcite-rich chimneys in the southern trough of Guaymas Basin were enriched in 18 O with respect to seawater by about 2.4‰ due to isotopic exchange with sedimentary and/or basaltic rocks. Carbon isotope values of calcite range from −9.6 to −14.0‰ δ 34 C pDB , indicating that carbon was derived in approximately equal quantities from the dissolution of marine carbonate minerals and the oxidation of organic matter during migration of hydrothermal fluid through the underlying sediment column. Statistically significant positive, linear correlations of δ 34 S , δ 34 C , and δ 18 O of sulfides and calcites with geographic location within the southern trough of Guaymas Basin are best explained by variations in water/rock ( w r "> wr ) ratios or sediment reactivity within subsurface alteration zones. Low w r "> wr ratios and the leaching of detrital carbonates and bacteriogenic sulfides at the southern vent sites result in relatively high δ 13 C and low δ 34 S in chimney carbonates and sulfides, respectively. In the north, where the depletion of alkalis in vent fluids indicates higher w r "> wr ratios, positive δ 34 S and more negative δ 13 c are due to increased contributions from organic matter oxidation and sulfate reduction reactions.

Geochimica et Cosmochimica Acta↗
USGS1991

Steady- and non-steady-state carbonate-silicate controls on atmospheric CO2

Two contrasting hypotheses have recently been proposed for the past long-term relation between atmospheric CO 2 and the carbonate-silicate geochemical cycle. One approach (Berner, 1990) suggests that CO 2 levels have varied in a manner that has maintained chemical weathering and carbonate sedimentation at a steady state with respect to tectonically controlled decarbonation reactions. A second approach (Raymo et al. , 1988), applied specificlly to the late Cenozoic, suggests a decrease in CO 2 caused by an uplift-induced increase in chemical weathering, without regard to the rate of decarbonation. According to the steady-state (first) hypothesis, increased weathering and carbonate sedimentation are generally associated with increasing atmospheric CO 2 , whereas the uplift (second) hypothesis implies decreasing CO 2 under the same conditions. An ocean-atmosphere-sediment model has been used to assess the response of atmospheric CO 2 and carbonate sedimentation to global perturbations in chemical weathering and decarbonation reactions. Although this assessment is theoretical and cannot yet be related to the geologic record, the model simulations compare steady-state and non-steady-state carbonate-silicate cycle response. The e-fold response time of the ‘CO 2 -weathering’ feedback mechanism is between 300 and 400 ka. The response of carbonate sedimentation is much more rapid. These response times provide a measure of the strength of steady-state assumptions, and imply that certain systematic relations are sustained throughout steady-state and non-steady-state scenarios for the carbonate-silicate cycle. The simulations suggest that feedbacks can maintain the system near a steady state, but that non-steady-state effects may contribute to long-term trends. The steady-state and uplift hypotheses are not necessarily incompatible over time scales of a few million years.

Quaternary Science Reviews↗
USGS2017

Human footprint affects US carbon balance more than climate change

The MC2 model projects an overall increase in carbon capture in conterminous United States during the 21st century while also simulating a rise in fire causing much carbon loss. Carbon sequestration in soils is critical to prevent carbon losses from future disturbances, and we show that natural ecosystems store more carbon belowground than managed systems do. Natural and human-caused disturbances affect soil processes that shape ecosystem recovery and competitive interactions between native, exotics, and climate refugees. Tomorrow's carbon budgets will depend on how land use, natural disturbances, and climate variability will interact and affect the balance between carbon capture and release.

Book chapter↗
USGS2012

Carbon dioxide stripping in aquaculture -- part II: development of gas transfer models

The basic mass transfer equation for gases such as oxygen and carbon dioxide can be derived from integration of the driving force equation. Because of the physical characteristics of the gas transfer processes, slightly different models are used for aerators tested under the non steady-state procedures, than for packed columns, or weirs. It is suggested that the standard condition for carbon dioxide should be 20 °C, 1 atm, CCO 2 =20 mg/kg, and XCO 2 =0.000285. The selection of the standard condition for carbon dioxide based on a fixed mole fraction ensures that standardized carbon dioxide transfer rates will be comparable even though the value of C* CO 2 in the atmosphere is increasing with time. The computation of mass transfer for carbon dioxide is complicated by the impact of water depth and gas phase enrichment on the saturation concentration within the unit, although the importance of either factor depends strongly on the specific type of aerator. For some types of aerators, the most accurate gas phase model remains to be determined for carbon dioxide. The assumption that carbon dioxide can be treated as a non-reactive gas in packed columns may apply for cold acidic waters but not for warm alkaline waters.

Aquacultural Engineering↗
USGS2021

Carbon stock losses and recovery observed for a mangrove ecosystem following a major hurricane in Southwest Florida

Studies integrating mangrove in-situ observations and remote sensing analysis for specific sites often lack precise estimates of carbon stocks over time frames that include disturbance events. This study quantifies change in mangrove area from 1985 to 2018 with Landsat time series analysis, estimates above and belowground stored carbon using field data, and evaluates aboveground carbon stock changes after the 2004 Category 4, Hurricane Charley, in J.N. “Ding” Darling National Wildlife Refuge. Two allometric equation methods yielding similar results were used to estimate aboveground carbon content in three mangrove species found in the refuge. Aboveground carbon contained 67 (SE = 2) MgC ha −1 with a total refuge estimate of 74,504 MgC in 2018. Sediment contained 259 (SE = 28) MgC ha −1 for a total of 288,008 MgC in the refuge. The initial reduction in mangrove area caused by Hurricane Charley was between 0.6% and 5.3%, equivalent to between 427 MgC and 3,599 MgC under three different scenarios of carbon loss. As a result of the hurricane, approximately 61 ha of mangroves were disturbed, of which 24 ha had recovered by 2018, with 37 ha (~3% of the pre-hurricane mangrove area) still not recovered 14 years after the event. The 37 ha of mangroves that have not recovered are located in a tidally restricted area of the refuge. A longer recovery time in this area will likely result in a greater loss of carbon storage than in the rest of the refuge.

Florida↗
USGS2009

U.S. Department of Energy's Regional Carbon Sequestration Partnership Program: Overview

The U.S. Department of Energy (DOE) has formed a nationwide network of seven regional partnerships to help determine the best approaches for capturing and permanently storing gases that can contribute to global climate change. The Regional Carbon Sequestration Partnerships (RCSPs) are tasked with determining the most suitable technologies, regulations, and infrastructure for carbon capture, transport, and storage in their areas of the country and parts of Canada. The seven partnerships include more than 350 state agencies, universities, national laboratories, private companies, and environmental organizations, spanning 42 states, two Indian nations, and four Canadian provinces. The Regional Partnerships initiative is being implemented in three phases: ???Characterization Phase (2003-2005): The objective was to collect data on CO 2 sources and sinks and develop the human capital to support and enable future carbon sequestration field tests and deployments. The completion of this Phase was marked by release of the Carbon Sequestration Atlas of the United States and Canada-Version 1 which included a common methodology for capacity assessment and reported over 3,000GT of storage capacity in saline formations, depleted oil and gas fields, and coal seams.???Validation Phase (2005-2009): The objective is to plan and implement small-scale (<1??million tons CO 2 ) field testing of storage technologies in areas determined to be favorable for carbon storage. The partnerships are currently conducting over 20 small-scale geologic field tests and 11 terrestrial field tests.???Development Phase (2008-2018): The primary objective is the development of large-scale (>1??million tons of CO 2 ) Carbon Capture and Storage (CCS) projects, which will demonstrate that large volumes of CO 2 can be injected safely, permanently, and economically into geologic formations representative of large storage capacity. Even though the RCSP Program is being implemented in three phases, it should be viewed as an integrated whole, with many of the goals and objectives transitioning from one phase to the next. Accomplishments and results from the Characterization Phase have helped to refine goals and activities in the Validation and Deployment Phases. The RCSP Program encourages and requires open information sharing among its members by sponsoring both general workshops and meetings to facilitate information exchange. Although each RCSP has its own objectives and field tests, mutual cooperation has been an important part of the Program thus far. The primary goal of the RCSP initiative is to promote the development of a regional framework and the infrastructure necessary to validate and deploy carbon sequestration technologies within each Partnership's region. ?? 2009 Elsevier Ltd. All rights reserved.

Conference Paper↗
USGS2020

Low O2 level enhances CH4-derived carbon flow into microbial communities in landfill cover soils

CH 4 oxidation in landfill cover soils plays a significant role in mitigating CH 4 release to the atmosphere. Oxygen availability and the presence of co-contaminants are potentially important factors affecting CH 4 oxidation rate and the fate of CH 4 -derived carbon. In this study, microbial populations that oxidize CH 4 and the subsequent conversion of CH 4 -derived carbon into CO 2 , soil organic C and biomass C were investigated in landfill cover soils at two O 2 tensions, i.e., O 2 concentrations of 21% (“sufficient”) and 2.5% (“limited”) with and without toluene. CH 4 -derived carbon was primarily converted into CO 2 and soil organic C in the landfill cover soils, accounting for more than 80% of CH 4 oxidized. Under the O 2 -sufficient condition, 52.9%–59.6% of CH 4 -derived carbon was converted into CO 2 (CE CO2-C ), and 29.1%–39.3% was converted into soil organic C (CE organic-C ). A higher CE organic-C and lower CE CO2-C occurred in the O 2 -limited environment, relative to the O 2 -sufficient condition. With the addition of toluene, the carbon conversion efficiency of CH 4 into biomass C and organic C increased slightly, especially in the O 2 -limited environment. A more complex microbial network was involved in CH 4 assimilation in the O 2 -limited environment than under the O 2 -sufficient condition. DNA-based stable isotope probing of the community with 13 CH 4 revealed that Methylocaldum and Methylosarcina had a higher relative growth rate than other type I methanotrophs in the landfill cover soils, especially at the low O 2 concentration, while Methylosinus was more abundant in the treatment with both the high O 2 concentration and toluene. These results indicated that O 2 -limited environments could prompt more CH 4 -derived carbon to be deposited into soils in the form of biomass C and organic C, thereby enhancing the contribution of CH 4 -derived carbon to soil community biomass and functionality of landfill cover soils (i.e. reduction of CO 2 emission).

Environmental Pollution↗
USGS2007

Carbon isotopic compositions of organic matter across continental Cretaceous-Tertiary (K-T) boundary sections: Implications for paleoenvironment after the K-T impact event

To assess the environmental perturbation induced by the impact event that marks the Cretaceous-Tertiary (K-T) boundary, concentrations and isotopic compositions of bulk organic carbon were determined in sedimentary rocks that span the terrestrial K-T boundary at Dogie Creek, Montana, and Brownie Butte, Wyoming in the Western Interior of the United States. The boundary clays at both sites are not bounded by coals. Although coals consist mainly of organic matter derived from plant tissue, siliceous sedimentary rocks, such as shale and clay, may contain organic matter derived from microbiota as well as plants. Coals record ??13C values of plant-derived organic matter, reflecting the ??13C value of atmospheric CO2, whereas siliceous sedimentary rocks record the ??13C values of organic matter derived from plants and microbiota. The microbiota ??13C value reflects not only the ??13C value of atmospheric CO2, but also biological productivity. Therefore, the siliceous rocks from these sites yields information that differs from that obtained previously from coal beds. Across the freshwater K-T boundary at Brownie Butte, the ??13C values decrease by 2.6??? (from - 26.15??? below the boundary clay to - 28.78??? above the boundary clay), similar to the trend in carbonate at marine K-T sites. This means that the organic ??13C values reflect the variation of ??13C of atmospheric CO2, which is in equilibrium with carbon isotopes at the ocean surface. Although a decrease in ??13C values is observed across the K-T boundary at Dogie Creek (from - 25.32??? below the boundary clay to - 26.11??? above the boundary clay), the degree of ??13C-decrease at Dogie Creek is smaller than that at Brownie Butte and that for marine carbonate. About 2??? decrease in ??13C of atmospheric CO2 was expected from the ??13C variation of marine carbonate at the K-T boundary. This ??13C-decrease of atmospheric CO2 should affect the ??13C values of organic matter derived from plant tissue. As such a decrease in ??13C value was not observed at Dogie Creek, a process that compensates the ??13C-decrease of atmospheric CO2 should be involved. For example, the enhanced contribution of 13C-enriched organic matter derived from algae in a high-productivity environment could be responsible. The ??13C values of algal organic matter become higher than, and thus distinguishable from, those of plant organic matter in situations with high productivity, where dissolved HCO3- becomes an important carbon source, as well as dissolved CO2. As the ??13C-decrease of atmospheric CO2 reflected a reduction of marine productivity, the compensation of the ??13C decrease by the enhanced activity of the terrestrial microbiota means that the microbiota at freshwater environment recovered more rapidly than those in the marine environment. A distinct positive ??13C excursion of 2??? in the K-T boundary clays is superimposed on the overall decreasing trend at Dogie Creek; this coincides with an increase in the content of organic carbon. We conclude that the K-T boundary clays include 13C-enriched organic matter derived from highly productive algae. Such a high biological productivity was induced by phenomena resulting from the K-T impact, such as nitrogen fertilization and/or eutrophication induced by enhanced sulfide formation. The high productivity recorded in the K-T boundary clays means that the freshwater environments (in contrast to marine environments) recovered rapidly enough to almost immediately (within 10??yr) respond to the impact-related environmental perturbations. ?? 2006 Elsevier B.V. All rights reserved.

Earth and Planetary Science Letters↗
USGS2012

Recycling of water, carbon, and sulfur during subduction of serpentinites: A stable isotope study of Cerro del Almirez, Spain

We use the concentrations and isotope compositions of water, carbon, and sulfur in serpentinites and their dehydration products to trace the cycling of volatiles during subduction. Antigorite serpentinites from the Cerro del Almirez complex, Spain, contain 9–12 wt.% H2O and 910 ± 730 ppm sulfur, and have bulk δ18O values of 8.6 ± 0.4‰, δD = − 54 ± 5‰, and δ34S = 5.0‰, consistent with serpentinization at temperatures of ~ 200 °C by seawater hydrothermal fluids in a seafloor setting. The serpentinites were dehydrated to chlorite–harzburgite (olivine + orthopyroxene + chlorite) at 700 °C and 1.6–1.9 GPa during subduction metamorphism, resulting in loss of water, and sulfur. The chlorite–harzburgites contain 5.7 ± 1.9 wt.% H2O, and have bulk δ18O = 8.0 ± 0.9‰, and δD = − 77 ± 11‰. The rocks contain 650 ± 620 ppm sulfur having δ34S = 1.2‰. Dehydration of serpentinite resulted in loss of 5 wt.% H2O having δ18O = 8–10‰ and δD = − 27 to − 65‰, and loss of 260 ppm sulfur as sulfate, having δ34S = 14.5‰. The contents and δ13C of total carbon in the two rock types overlap, with a broad trend of decreasing carbon contents and δ13C from ~ 1300 to 200 ppm and − 9.6 to − 20.2‰. This reflects mixing between reduced carbon in the rocks (210 ppm, δ13C ≈ − 26‰) and seawater-derived carbonate (δ13C ≈ − 1‰). Our results indicate: 1) Serpentinized oceanic peridotites carry significant amounts of isotopically fractionated water, carbon and sulfur into subduction zones; 2) Subduction of serpentinites to high P and T results in loss of water, and sulfur, which can induce melting and contribute to 18O, D, and 34S enrichments and oxidation of the sub-arc mantle wedge; and 3) Isotopically fractionated water, carbon, and sulfur in serpentinite dehydration products are recycled deeper into the mantle where they can contribute to isotope heterogeneities and may be significant for volatile budgets of the deep Earth.

Cerro Del Almirez;Betic Cordillera In Southern Spa↗
USGS2013

Determination of diffusion coefficients of carbon dioxide in water between 268 and 473 K in a high-pressure capillary optical cell with in situ Raman spectroscopic measurements

Accurate values of diffusion coefficients for carbon dioxide in water and brine at reservoir conditions are essential to our understanding of transport behavior of carbon dioxide in subsurface pore space. However, the experimental data are limited to conditions at low temperatures and pressures. In this study, diffusive transfer of carbon dioxide in water at pressures up to 45 MPa and temperatures from 268 to 473 K was observed within an optical capillary cell via time-dependent Raman spectroscopy. Diffusion coefficients were estimated by the least-squares method for the measured variations in carbon dioxide concentration in the cell at various sample positions and time. At the constant pressure of 20 MPa, the measured diffusion coefficients of carbon dioxide in water increase with increasing temperature from 268 to 473 K. The relationship between diffusion coefficient of carbon dioxide in water [D(CO 2 ) in m 2 /s] and temperature (T in K) was derived with Speedy–Angell power-law approach as: D(CO 2 )=D 0 [T/Ts-1] m where D 0 = 13.942 × 10 −9 m 2 /s, Ts = 227.0 K, and m = 1.7094. At constant temperature, diffusion coefficients of carbon dioxide in water decrease with pressure increase. However, this pressure effect is rather small (within a few percent).

Geochimica et Cosmochimica Acta↗
USGS2021

A reactive transport approach to modeling cave seepage water chemistry I: Carbon isotope transformations

The majority of Critical Zone research has emphasized silicate lithologies, which are typified by relatively slow rates of reactivity and incongruent weathering. However, the relatively simpler weathering of carbonate-dominated lithology can result in secondary mineral deposits, such as speleothems, which provide a long-term archive for Critical Zone processes. In particular, carbon isotopic variability in speleothems has the potential to provide records of changes in vegetation, soil respiration, carbon stabilization in deep soils, and/or chemical weathering in the host rock. Despite this opportunity to reconstruct many Critical Zone processes, multiple influences can also make interpretion of these speleothem carbon isotope records challenging. The integration of observational data and simulations specific to karst systems offers an interpretive framework for these unique time-averaged records accumulated through the evolution of carbonate landscapes. Here, we present a forward and process-based reactive transport simulation based on a multi-year monitoring study of Blue Spring Cave in central Tennessee, USA. The simulations describe the fluid-driven weathering of limestone including explicit tracking of dissolved calcium, stable carbon, and radiocarbon isotope ratios based on reaction rates calibrated through laboratory batch reaction data. We find that calcium concentrations and radiocarbon isotope ratios are strongly influenced by the combination of fluid flow rate and soil CO 2 content, and require rapid gas phase communication between the overlying soil boundary condition and interior karst to sustain both elevated limestone weathering rates and relatively modern radiocarbon signatures. Stable carbon isotopes are largely dictated by temperature-dependent equilibrium fractionation among contemporaneous species. These simulations are extended to a wide range of parameter space to demonstrate the environmental factors that these isotope proxies record.

Geochimica et Cosmochimica Acta↗