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At least 451 records · Page 25Linked to original sources

Oxygenation of a karst subterranean estuary during a tropical cyclone: Mechanisms and implications for the carbon cycle

Seasonal precipitation affects carbon turnover and methane accumulation in karst subterranean estuaries, the region of coastal carbonate aquifers where hydrologic and biogeochemical processes regulate material exchange between the land and ocean. However, the impact that tropical cyclones exert on subsurface carbon cycling within karst landscapes is poorly understood. Here, we present 5-month-long hydrologic and chemical records from 1 and 2 km inland from the coastline within the Ox Bel Ha Cave System in the northeastern Yucatan Peninsula. The record encompasses wet and dry seasons and includes the impact of rainfall during the development of Tropical Storm Hanna in October 2014 . Methane accumulated in highest concentrations at the inland site, especially during the wet season preceding the storm. Intense rainfall led to episodic increases in water level and salinity shifts at both sites, indicating a spatially widespread hydrologic response. The most profound storm effect was a ~ 0.8 mg L −1 pulse of dissolved oxygen that declined to zero within 2 weeks and corresponded with a reduction of methane. A positive shift in methane's stable carbon isotope content from −62.6‰ ± 0.6‰ before the storm to −44.0‰ ± 2.4‰ after the storm indicates microbial methane oxidation was a mechanism for the loss of groundwater methane. Post-storm methane concentrations did not recover to pre-storm levels during the observation period, suggesting tropical cyclones have long-lasting (months) effects on the carbon cycle. Compared to seasonal effects, mixing and oxygen inputs during storm-induced hydrologic forcing have an outsized biogeochemical influence within stratified coastal aquifers.

Ox Bel Ha Cave System, Yucatan Peninsula↗

USGS44, a new high-purity calcium carbonate reference material for δ13C measurements

Rationale The stable carbon isotopic ( δ 13 C) reference material (RM) LSVEC Li 2 CO 3 has been found to be unsuitable for δ 13 C standardization work because its δ 13 C value increases with exposure to atmospheric CO 2 . A new CaCO 3 RM, USGS44, has been prepared to alleviate this situation. Methods USGS44 was prepared from 8 kg of Merck high-purity CaCO 3 . Two sets of δ 13 C values of USGS44 were determined. The first set of values was determined by online combustion, continuous-flow (CF) isotope-ratio mass spectrometry (IRMS) of NBS 19 CaCO 3 ( δ 13 C VPDB = +1.95 milliurey (mUr) exactly, where mUr = 0.001 = 1‰), and LSVEC Li 2 CO 3 ( δ 13 C VPDB = −46.6 mUr exactly), and normalized to the two-anchor δ 13 C VPDB-LSVEC isotope-delta scale. The second set of values was obtained by dual-inlet (DI)-IRMS of CO 2 evolved by reaction of H 3 PO 4 with carbonates, corrected for cross contamination, and normalized to the single-anchor δ 13 C VPDB scale. Results USGS44 is stable and isotopically homogeneous to within 0.02 mUr in 100-μg amounts. It has a δ 13 C VPDB-LSVEC value of −42.21 ± 0.05 mUr. Single-anchor δ 13 C VPDB values of −42.08 ± 0.01 and −41.99 ± 0.02 mUr were determined by DI-IRMS with corrections for cross contamination. Conclusions The new high-purity, well-homogenized calcium carbonate isotopic reference material USGS44 is stable and has a δ 13 C VPDB-LSVEC value of −42.21 ± 0.05 mUr for both EA/IRMS and DI-IRMS measurements. As a carbonate relatively depleted in 13 C, it is intended for daily use as a secondary isotopic reference material to normalize stable carbon isotope delta measurements to the δ 13 C VPDB-LSVEC scale. It is useful in quantifying drift with time, determining mass-dependent isotopic fractionation (linearity correction), and adjusting isotope-ratio-scale contraction. Due to its fine grain size (smaller than 63 μm), it is not suitable as a δ 18 O reference material. A δ 13 C VPDB-LSVEC value of −29.99 ± 0.05 mUr was determined for NBS 22 oil.

Rapid Communications in Mass Spectrometry↗

Factors Affecting 14C Ages of Lacustrine Carbonates: Timing and Duration of the Last Highstand Lake in the Lahontan Basin

Two processes contribute to inaccurate 14C age estimates of carbonates precipitated within the Lahontan basin, NevadaCalifornia: low initial 14C/C ratios in lake water (reservoir effect) and addition of modern carbon to calcium carbonate after its precipitation. The mast reliable set of 14C ages on carbonates from elevations > 1310 m in the Pyramid and Walker Lake subbasins indicate that lakes in all seven Lahontan subbasins coalesced ???14,200 14C yr B.P. forming Lake Lahontan. Lake Lahontan achieved its 1330-m highstand elevation by ???13,800 14 C yr B.P. and receded to 1310 m by ???13,700 14C yr B.P. Calculations, based on measured carbonate-accumulation rates, of the amount of time Lake Lahontan exceeded 1310 and 1330 m (500 and 50 yr) are consistent with this chronology. The timing of the Lake Lahontan highstand is of interest because of the linkage of highstand climates with proximity to the polar jet stream. The brevity of the Lahontan highstand is interpreted to indicate that the core of the southern branch of the polar jet stream remained only briefly over the Lahontan basin.

Quaternary Research↗

Contemporary carbon dynamics in terrestrial ecosystems in the Southeastern Plains of the United States

Quantifying carbon dynamics over large areas is frequently hindered by the lack of consistent, high-quality, spatially explicit land use and land cover change databases and appropriate modeling techniques. In this paper, we present a generic approach to address some of these challenges. Land cover change information in the Southeastern Plains ecoregion was derived from Landsat data acquired in 1973, 1980, 1986, 1992, and 2000 within 11 randomly located 20-km × 20-km sample blocks. Carbon dynamics within each of the sample blocks was simulated using the General Ensemble Biogeochemical Modeling System (GEMS), capable of assimilating the variances and covariance of major input variables into simulations using an ensemble approach. Results indicate that urban and forest areas have been increasing, whereas agricultural land has been decreasing since 1973. Forest clear-cutting activity has intensified, more than doubling from 1973 to 2000. The Southeastern Plains has been acting as a carbon sink since 1973, with an average rate of 0.89 Mg C/ha/yr. Biomass, soil organic carbon (SOC), and harvested materials account for 56%, 34%, and 10% of the sink, respectively. However, the sink has declined continuously during the same period owing to forest aging in the northern part of the ecoregion and increased forest clear-cutting activities in the south. The relative contributions to the sink from SOC and harvested materials have increased, implying that these components deserve more study in the future. The methods developed here can be used to quantify the impacts of human management activities on the carbon cycle at landscape to global scales.

Environmental Management↗

Woody debris volume depletion through decay: implications for biomass and carbon accounting

Woody debris decay rates have recently received much attention because of the need to quantify temporal changes in forest carbon stocks. Published decay rates, available for many species, are commonly used to characterize deadwood biomass and carbon depletion. However, decay rates are often derived from reductions in wood density through time, which when used to model biomass and carbon depletion are known to underestimate rate loss because they fail to account for volume reduction (changes in log shape) as decay progresses. We present a method for estimating changes in log volume through time and illustrate the method using a chronosequence approach. The method is based on the observation, confirmed herein, that decaying logs have a collapse ratio (cross-sectional height/width) that can serve as a surrogate for the volume remaining. Combining the resulting volume loss with concurrent changes in wood density from the same logs then allowed us to quantify biomass and carbon depletion for three study species. Results show that volume, density, and biomass follow distinct depletion curves during decomposition. Volume showed an initial lag period (log dimensions remained unchanged), even while wood density was being reduced. However, once volume depletion began, biomass loss (the product of density and volume depletion) occurred much more rapidly than density alone. At the temporal limit of our data, the proportion of the biomass remaining was roughly half that of the density remaining. Accounting for log volume depletion, as demonstrated in this study, provides a comprehensive characterization of deadwood decomposition, thereby improving biomass-loss and carbon-accounting models.

Minnesota↗

Particulate organic matter quality influences nitrate retention and denitrification in stream sediments: evidence from a carbon burial experiment

Organic carbon supply is linked to nitrogen transformation in ecosystems. However, the role of organic carbon quality in nitrogen processing is not as well understood. We determined how the quality of particulate organic carbon (POC) influenced nitrogen transformation in stream sediments by burying identical quantities of varying quality POC (northern red oak ( Quercus rubra ) leaves, red maple ( Acer rubrum ) leaves, red maple wood) in stream mesocosms and measuring the effects on nitrogen retention and denitrification compared to a control of combusted sand. We also determined how POC quality affected the quantity and quality of dissolved organic carbon (DOC) and dissolved oxygen concentration in groundwater. Nitrate and total dissolved nitrogen (TDN) retention were assessed by comparing solute concentrations and fluxes along groundwater flow paths in the mesocosms. Denitrification was measured by in situ changes in N 2 concentrations (using MIMS) and by acetylene block incubations. POC quality was measured by C:N and lignin:N ratios and DOC quality was assessed by fluorescence excitation emission matrix spectroscopy. POC quality had strong effects on nitrogen processing. Leaf treatments had much higher nitrate retention, TDN retention and denitrification rates than the wood and control treatments and red maple leaf burial resulted in higher nitrate and TDN retention rates than burial of red oak leaves. Leaf, but not wood, burial drove pore water to severe hypoxia and leaf treatments had higher DOC production and different DOC chemical composition than the wood and control treatments. We think that POC quality affected nitrogen processing in the sediments by influencing the quantity and quality of DOC and redox conditions. Our results suggest that the type of organic carbon inputs can affect the rates of nitrogen transformation in stream ecosystems.

Wisconsin↗

Methane hydrate - A major reservoir of carbon in the shallow geosphere?

Methane hydrates are solids composed of rigid cages of water molecules that enclose methane. Sediment containing methane hydrates is found within specific pressure-temperature conditions that occur in regions of permafrost and beneath the sea in outer continental margins. Because methane hydrates are globally widespread and concentrate methane within the gas-hydrate structure, the potential amount of methane present in the shallow geosphere at subsurface depths of < ???2000 m is very large. However, estimates of the amount are speculative and range over about three orders of magnitude, from 2 ?? 103 to 4 ?? 106 Gt (gigatons = 1015 g) of carbon, depending on the assumptions made. The estimate I favor is ??? 1 ?? 104 Gt of carbon. The estimated amount of organic carbon in the methane-hydrate reservoir greatly exceeds that in many other reservoirs of the global carbon cycle - for example, the atmosphere (3.6 Gt); terrestrial biota (830 Gt); terrestrial soil, detritus and peat (1960 Gt); marine biota (3 Gt); and marine dissolved materials (980 Gt). In fact, the amount of carbon may exceed that in all fossil fuel deposits (5 ?? 103 Gt). Because methane hydrates contain so much methane and occur in the shallow geosphere, they are of interest as a potential resource of natural gas and as a possible source of atmospheric methane released by global warming. As a potential resource, methane hydrates pose both engineering and production problems. As a contributor to a changing global climate, destabilized methane hydrates, particularly those in shallow, nearshore regions of the Arctic Ocean, may have some effect, but this effect will probably be minimal, at least during the next 100 years. ?? 1988.

Chemical Geology↗

Fractionation of carbon and hydrogen isotopes by methane-oxidizing bacteria

Carbon isotopic analysis of methane has become a popular technique in the exploration for oil and gas because it can be used to differentiate between thermogenic and microbial gas and can sometimes be used for gas-source rock correlations. Methane-oxidizing bacteria, however, can significantly change the carbon isotopic composition of methane; the origin of gas that has been partially oxidized by these bacteria could therefore be misinterpreted. We cultured methane-oxidizing bacteria at two different temperatures and monitored the carbon and hydrogen isotopic compositions of the residual methane. The residual methane was enriched in both 13 C and D. For both isotopic species, the enrichment at equivalent levels of conversion was greater at 26°C than at 11.5°C. The change in δD relative to the change in δ 13 C was independent of temperature within the range studied. One culture exhibited a change in the fractionation pattern for carbon (but not for hydrogen) midway through the experiment, suggesting that bacterial oxidation of methane may occur via more than one pathway. The change in the δD value for the residual methane was from 8 to 14 times greater than the change in the δ 13 C value, indicating that combined carbon and hydrogen isotopic analysis may be an effective way of identifying methane which has been subjected to partial oxidation by bacteria.

Geochimica et Cosmochimica Acta↗

Shrubland carbon sink depends upon winter water availability in the warm deserts of North America

Global-scale studies suggest that dryland ecosystems dominate an increasing trend in the magnitude and interannual variability of the land CO 2 sink. However, such model-based analyses are poorly constrained by measured CO 2 exchange in open shrublands, which is the most common global land cover type, covering ∼14% of Earth’s surface. Here we evaluate how the amount and seasonal timing of water availability regulate CO 2 exchange between shrublands and the atmosphere. We use eddy covariance data from six US sites across the three warm deserts of North America with observed ranges in annual precipitation of ∼100–400mm, annual temperatures of 13–18°C, and records of 2–8 years (33 site-years in total). The Chihuahuan, Sonoran and Mojave Deserts present gradients in both mean annual precipitation and its seasonal distribution between the wet-winter Mojave Desert and the wet-summer Chihuahuan Desert. We found that due to hydrologic losses during the wettest summers in the Sonoran and Chihuahuan Deserts, evapotranspiration (ET) was a better metric than precipitation of water available to drive dryland CO 2 exchange. In contrast with recent synthesis studies across diverse dryland biomes, we found that NEP could not be directly predicted from ET due to wintertime decoupling of the relationship between ecosystem respiration (R eco ) and gross ecosystem productivity (GEP). Ecosystem water use efficiency (WUE=GEP/ET) did not differ between winter and summer. Carbon use efficiency (CUE=NEP/GEP), however, was greater in winter because R eco returned a smaller fraction of carbon to the atmosphere (23% of GEP) than in summer (77%). Combining the water-carbon relations found here with historical precipitation since 1980, we estimate that lower average winter precipitation during the 21st century reduced the net carbon sink of the three deserts by an average of 6.8TgC yr 1 . Our results highlight that winter precipitation is critical to the annual carbon balance of these warm desert shrublands.

Agricultural and Forest Meteorology↗

Evaluating drivers of environmental change in a lake sediment core: Insights from spectroscopic metrics of water-extractable organic matter and stable carbon isotopes

Freshwater lakes play a critical role in the global carbon cycle by storing and transforming organic matter (OM) from both terrestrial and aquatic sources. Small lakes in northern temperate regions, despite their limited surface area, disproportionately influence regional carbon budgets. Buried sediments integrate OM inputs over time and archive ecosystem responses to natural and anthropogenic disturbances. However, the direction and magnitude of recent environmental changes on sediment carbon (C) dynamics remain poorly understood. A 23-cm core was collected from a small temperate lake in northeastern USA to evaluate sediment OM content and composition over timescales relevant to historical land-use change, damming, and recovery from acid deposition. Patterns in OM burial and source contributions were revealed via elemental and isotopic analyses of bulk OM and ultraviolet-visible spectrophotometry of water-extractable organic matter (WEOM). The optical metrics expanded observations of likely OM sources beyond the information gained from bulk carbon metrics (total carbon, δ 13 C). The aromaticity of WEOM increased downcore, which is consistent with a shift from increased terrestrial inputs during early logging and damming activity (pre ∼1920) to more microbial-derived OM in recent surficial sediments. Future applications of WEOM optical properties as complements to traditional geochemical metrics can enhance interpretations of lake ecosystem responses recorded in lake sediments to environmental perturbations in temperate lakes.

New York↗

Carbon and geochemical properties of cryosols on the North Slope of Alaska

Cryosols contain roughly 1700 Gt of Soil organic carbon (SOC) roughly double the carbon content of the atmosphere. As global temperature rises and permafrost thaws, this carbon reservoir becomes vulnerable to microbial decomposition, resulting in greenhouse gas emissions that will amplify anthropogenic warming. Improving our understanding of carbon dynamics in thawing permafrost requires more data on carbon and nitrogen content, soil physical and chemical properties and substrate quality in cryosols. We analyzed five permafrost cores obtained from the North Slope of Alaska during the summer of 2009. The relationship between SOC and soil bulk density can be adequately represented by a logarithmic function. Gas fluxes at &minus; 5 &deg;C and 5 &deg;C were measured to calculate the temperature response quotient (Q 10 ). Q 10 and the respiration per unit soil C were higher in permafrost-affected soils than that in the active layer, suggesting that decomposition and heterotrophic respiration in cryosols may contribute more to global warming.

Alaska↗

Simulation of dissolved organic carbon flux in the Penobscot Watershed, Maine

Dissolved organic carbon (DOC) is an important component of the carbon cycle as a measure of the hydrological transport of carbon between terrestrial carbon pools into soil pools and eventually into streams. As a result, changes in DOC in rivers and streams may indicate alterations in the storage of terrestrial carbon. Exploring the complex interactions between biogeochemical cycling and hydrologic processes, as well as the micro-climate variabilities that impact the rate of DOC fluxes, are challenging because the information is not readily available from in-situ measurements or from empirical models alone. This is particularly true of large-scale watersheds. The Penobscot Watershed is the largest watershed of the Gulf of Maine and the second largest in New England. Its typical soils, with high organic matter and a large forested and wetland landscape, result in higher DOC fluxes than what has been observed previously for most rivers in the northern temperate or boreal zones (Hope et al., 1994; Mulholland, 1997; Aitkenhead and McDowell, 2000). In this study, we emphasized the simulation of streamflow and DOC fluxes from the Penobscot Watershed (and several tributaries within the Penobscot Watershed) using the spatially distributed process-based Regional Hydro-Ecological Simulation System (RHESSys) model. Simulated results were evaluated using field measurements (streamflow, DOC fluxes) and remotely sensed products (Net Primary Production (NPP) and Leaf Area Index (LAI) from Moderate Resolution Imaging Spectroradiometer (MODIS). The average DOC flux for the Penobscot Watershed during 2004-2012 using the RHESSys model was 69 kg C/ha/year. The RHESSys simulated DOC flux is shown to correlate well with observed values, as well as with results previously reported from the empirical Load Estimator (LOADEST) model (71 kg C/ha/year) for 2004-2007 ( Huntington and Aiken, 2013). Our simulated results also show a temporal variation in the amount of DOC flux, indicating that the antecedent DOC concentration from one year can impact the DOC export in following years. Thus, DOC concentration is positively correlated with streamflow and antecedent precipitation, in agreement with previous studies (Ågren et al., 2010; Huntington and Aiken, 2013; Tian et al., 2013 ). The successful application of the rigorous RHESSys model in the Penobscot Watershed makes it a reasonable platform to test future scenarios impacting the hydrology and biogeochemistry within similar large complex watersheds.

Maine↗

Estimating aboveground forest biomass carbon and fire consumption in the U.S. Utah High Plateaus using data from the Forest Inventory and Analysis program, Landsat, and LANDFIRE

The concentrations of CO 2 and other greenhouse gases in the atmosphere have been increasing and greatly affecting global climate and socio-economic systems. Actively growing forests are generally considered to be a major carbon sink, but forest wildfires lead to large releases of biomass carbon into the atmosphere. Aboveground forest biomass carbon (AFBC), an important ecological indicator, and fire-induced carbon emissions at regional scales are highly relevant to forest sustainable management and climate change. It is challenging to accurately estimate the spatial distribution of AFBC across large areas because of the spatial heterogeneity of forest cover types and canopy structure. In this study, Forest Inventory and Analysis (FIA) data, Landsat, and Landscape Fire and Resource Management Planning Tools Project (LANDFIRE) data were integrated in a regression tree model for estimating AFBC at a 30-m resolution in the Utah High Plateaus. AFBC were calculated from 225 FIA field plots and used as the dependent variable in the model. Of these plots, 10% were held out for model evaluation with stratified random sampling, and the other 90% were used as training data to develop the regression tree model. Independent variable layers included Landsat imagery and the derived spectral indicators, digital elevation model (DEM) data and derivatives, biophysical gradient data, existing vegetation cover type and vegetation structure. The cross-validation correlation coefficient ( r value) was 0.81 for the training model. Independent validation using withheld plot data was similar with r value of 0.82. This validated regression tree model was applied to map AFBC in the Utah High Plateaus and then combined with burn severity information to estimate loss of AFBC in the Longston fire of Zion National Park in 2001. The final dataset represented 24 forest cover types for a 4 million ha forested area. We estimated a total of 353 Tg AFBC with an average of 87 MgC/ha in the Utah High Plateaus. We also estimated that 8054 Mg AFBC were released from 2.24 km 2 burned forest area in the Longston fire. These results demonstrate that an AFBC spatial map and estimated biomass carbon consumption can readily be generated using existing database. The methodology provides a consistent, practical, and inexpensive way for estimating AFBC at 30-m resolution over large areas throughout the United States.

Ecological Indicators↗

Resolving model parameter values from carbon and nitrogen stock measurements in a wide range of tropical mature forests using nonlinear inversion and regression trees

Objectively assessing the performance of a model and deriving model parameter values from observations are critical and challenging in landscape to regional modeling. In this paper, we applied a nonlinear inversion technique to calibrate the ecosystem model CENTURY against carbon (C) and nitrogen (N) stock measurements collected from 39 mature tropical forest sites in seven life zones in Costa Rica. Net primary productivity from the Moderate-Resolution Imaging Spectroradiometer (MODIS), C and N stocks in aboveground live biomass, litter, coarse woody debris (CWD), and in soils were used to calibrate the model. To investigate the resolution of available observations on the number of adjustable parameters, inversion was performed using nine setups of adjustable parameters. Statistics including observation sensitivity, parameter correlation coefficient, parameter sensitivity, and parameter confidence limits were used to evaluate the information content of observations, resolution of model parameters, and overall model performance. Results indicated that soil organic carbon content, soil nitrogen content, and total aboveground biomass carbon had the highest information contents, while measurements of carbon in litter and nitrogen in CWD contributed little to the parameter estimation processes. The available information could resolve the values of 2-4 parameters. Adjusting just one parameter resulted in under-fitting and unacceptable model performance, while adjusting five parameters simultaneously led to over-fitting. Results further indicated that the MODIS NPP values were compressed as compared with the spatial variability of net primary production (NPP) values inferred from inverse modeling. Using inverse modeling to infer NPP and other sensitive model parameters from C and N stock observations provides an opportunity to utilize data collected by national to regional forest inventory systems to reduce the uncertainties in the carbon cycle and generate valuable databases to validate and improve MODIS NPP algorithms.

Ecological Modelling↗

Widespread kelp-derived carbon in pelagic and benthic nearshore fishes

Kelp forests provide habitat for diverse and abundant fish assemblages, but the extent to which kelp provides a source of energy to fish and other predators is unclear. To examine the use of kelp-derived energy by fishes we estimated the contribution of kelp- and phytoplankton-derived carbon using carbon (δ 13 C) and nitrogen (δ 15 N) isotopes measured in muscle tissue. Benthic-foraging kelp greenling (Hexagrammos decagrammus) and pelagic-foraging black rockfish (Sebastes melanops) were collected at eight sites spanning ∼35 to 60°N from the California Current (upwelling) to Alaska Coastal Current (downwelling) in the northeast Pacific Ocean. Muscle δ 13 C values were expected to be higher for fish tissue primarily derived from kelp, a benthic macroalgae, and lower for tissue primarily derived from phytoplankton, pelagic microalgae. Muscle δ 13 C values were higher in benthic-feeding kelp greenling than in pelagic-feeding black rockfish at seven of eight sites, indicating more kelp-derived carbon in greenling as expected. Estimates of kelp carbon contributions ranged from 36 to 89% in kelp greenling and 32 to 65% in black rockfish using carbon isotope mixing models. Isotopic evidence suggests that these two nearshore fishes routinely derive energy from kelp and phytoplankton, across coastal upwelling and downwelling systems. Thus, the foraging mode of nearshore predators has a small influence on their ultimate energy source as energy produced by benthic macroalgae and pelagic microalgae were incorporated in fish tissue regardless of feeding mode and suggest strong and widespread benthic-pelagic coupling. Widespread kelp contributions to benthic- and pelagic-feeding fishes suggests that kelp energy provides a benefit to nearshore fishes and highlights the potential for kelp and fish production to be linked.

Estuarine, Coastal and Shelf Science↗

Delineation of Magnesium-rich Ultramafic Rocks Available for Mineral Carbon Sequestration in the United States

The 2005 Intergovernmental Panel on Climate Change report on Carbon Dioxide Capture and Storage suggested that a major gap in mineral carbon sequestration is locating the magnesium-silicate bedrock available to sequester CO2. It is generally known that silicate minerals with high concentrations of magnesium are suitable for mineral carbonation. However, no assessment has been made covering the entire United States detailing their geographical distribution and extent, or evaluating their potential for use in mineral carbonation. Researchers at Columbia University and the U.S. Geological Survey have developed a digital geologic database of ultramafic rocks in the continental United States. Data were compiled from varied-scale geologic maps of magnesium-silicate ultramafic rocks. These rock types are potentially suitable as source material for mineral carbon-dioxide sequestration. The focus of the national-scale map is entirely on suitable ultramafic rock types, which typically consist primarily of olivine and serpentine minerals. By combining the map with digital datasets that show non-mineable lands (such as urban areas and National Parks), estimates on potential depth of a surface mine, and the predicted reactivities of the mineral deposits, one can begin to estimate the capacity for CO2 mineral sequestration within the United States. ?? 2009 Elsevier Ltd. All rights reserved.

Conference Paper↗

Carbon stock trends of baldcypress knees along climate gradients of the Mississippi River Alluvial Valley using allometric methods

Carbon stock trends of the knees of Taxodium distichum likely vary across climate gradients of the southeastern United States and contribute an unknown quantity of “teal” carbon to inland freshwater wetlands. Knee metrics (e.g., density, height, biomass) were measured in mixed T. distichum swamps across the Mississippi River Alluvial Valley (MRAV) from Illinois to Louisiana. Based on their geometric similarity to a cone, the biomasses of field knees were estimated by relating the volume of their measured field dimensions to lab-measured water displacement volume and biomass via volume/mass regressions (biomass (g) = 7.2230149 + 0.292902 × volume). Knees had greater height in flooded conditions (maximum height = 163 cm; Goose Lake, Arkansas), and also in climate normal environments of mid-range precipitation and temperature (p < 0.0001). Overall, knee biomass ha−1 was 7.5 times greater in flooded vs. not flooded conditions (34.6 ± 7.3 vs. 4.6 ± 1.0 Mg ha−1, respectively). The overall mean of knee carbon biomass stock was substantial (flooded vs. not flooded conditions: 18.1 ± 3.7 Mg C ha−1 to 2.9 ± 0.7 Mg C ha−1, respectively; knee/tree live standing biomass: 17.9–5.2%, respectively). Clearly, T. distichum knees should not be ignored in blue (teal) carbon discussions of wetlands. Because knees respond to climate normal conditions, hotter/drier environments in the MRAV could lead to a decline in the contribution of knee carbon stock in the southeastern United States.

Mississippi River Alluvial Valley↗

ATR-FTIR spectroscopic characterization of coexisting carbonate surface complexes on hematite

The speciation of carbonate adsorbed to hematite in air-equilibrated aqueous solutions has been studied using ATR-FTIR spectroscopy. Samples were measured over a range of pH conditions, at 0.1 M NaCl and at low ionic strength, and in H2O and D2O solutions to permit a multispecies analysis of the data. Second-derivative analyses and fits to the spectra indicate the presence of two major and two minor surface-bound carbonate species. The two major complexes coexist at near-neutral pH and low ionic strength. One of these two complexes is relatively sensitive to ionic strength, being displaced at 0.1 M NaCl, whereas the other is not. Comparison of experimental to DFT/MO-calculated frequencies suggest these two major species to be (a) a monodentate binuclear inner-sphere carbonate surface complex, and (b) a fully or partially solvated carbonate (CO32-) species that is symmetry broken and appears to reside in the structured vicinal water layers at the hematite-water interface, retained by hydrogen bonding and/or other forces. Minor carbonate complexes include diffuse layer CO32- and an unidentified inner-sphere species. Both of the dominant species observed here are likely to be significant controls of the surface charge and sorptive properties of Fe-oxides. Copyright ?? 2005 Elsevier Ltd.

Geochimica et Cosmochimica Acta↗