SEARCH · Search USGS

Results for “Carbon”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 73 records · Page 4Linked to original sources

USGS2013

Reorganization of vegetation, hydrology and soil carbon after permafrost degradation across heterogeneous boreal landscapes

The diversity of ecosystems across boreal landscapes, successional changes after disturbance and complicated permafrost histories, present enormous challenges for assessing how vegetation, water and soil carbon may respond to climate change in boreal regions. To address this complexity, we used a chronosequence approach to assess changes in vegetation composition, water storage and soil organic carbon (SOC) stocks along successional gradients within four landscapes: (1) rocky uplands on ice-poor hillside colluvium, (2) silty uplands on extremely ice-rich loess, (3) gravelly–sandy lowlands on ice-poor eolian sand and (4) peaty–silty lowlands on thick ice-rich peat deposits over reworked lowland loess. In rocky uplands, after fire permafrost thawed rapidly due to low ice contents, soils became well drained and SOC stocks decreased slightly. In silty uplands, after fire permafrost persisted, soils remained saturated and SOC decreased slightly. In gravelly–sandy lowlands where permafrost persisted in drier forest soils, loss of deeper permafrost around lakes has allowed recent widespread drainage of lakes that has exposed limnic material with high SOC to aerobic decomposition. In peaty–silty lowlands, 2–4 m of thaw settlement led to fragmented drainage patterns in isolated thermokarst bogs and flooding of soils, and surface soils accumulated new bog peat. We were not able to detect SOC changes in deeper soils, however, due to high variability. Complicated soil stratigraphy revealed that permafrost has repeatedly aggraded and degraded in all landscapes during the Holocene, although in silty uplands only the upper permafrost was affected. Overall, permafrost thaw has led to the reorganization of vegetation, water storage and flow paths, and patterns of SOC accumulation. However, changes have occurred over different timescales among landscapes: over decades in rocky uplands and gravelly–sandy lowlands in response to fire and lake drainage, over decades to centuries in peaty–silty lowlands with a legacy of complicated Holocene changes, and over centuries in silty uplands where ice-rich soil and ecological recovery protect permafrost.

Alaska↗

USGS2014

USGS Arctic Ocean Carbon Cruise 2012: Field Activity L-01-12-AR to collect carbon data in the Arctic Ocean, August-September 2012

From August 25 to September 27, 2012, the United States Coast Guard Cutter (USCGC) Healy was part of an Extended Continental Shelf Project to determine the limits of the extended continental shelf in the Arctic. On a non-interference basis, a USGS ocean acidification team participated on the cruise to collect baseline water data in the Arctic. The collection of data extended from coastal waters near Barrow, Alaska, to 83°2'N., -175°36'W., and southward back to coastal waters near Barrow and on to Dutch Harbor, Alaska. As a consequence, a number of hypotheses were tested and questions asked associated with ocean acidification, including: What is the saturation state for different parts of the basin? What factors drive the saturation state in the different parts of the basin? How does saturation state compare to other regions? How do the carbon fluxes compare in the different parts of the basin? What is the buffering capacity of the water (Revelle factor)? What kind of variability does carbon demonstrate in the Arctic (near shore versus offshore and diurnal)? During the cruise, underway continuous and discrete water samples were collected, and discrete water samples were collected at stations to document the carbonate chemistry of the Arctic waters and quantify the saturation state of seawater with respect to calcium carbonate. These data are critical for providing baseline information in areas where no data have existed prior and will also be used to test existing models and predict future trends.

Arctic Ocean↗

USGS2017

Baseline and projected future carbon storage and carbon fluxes in ecosystems of Hawai‘i

This assessment was conducted to fulfill the requirements of section 712 of the Energy Independence and Security Act of 2007 and to improve understanding of factors influencing carbon balance in ecosystems of Hawai‘i. Ecosystem carbon storage, carbon fluxes, and carbon balance were examined for major terrestrial ecosystems on the seven main Hawaiian islands in two time periods: baseline (from 2007 through 2012) and future (projections from 2012 through 2061). The assessment incorporated observed data, remote sensing, statistical methods, and simulation models. The national assessment has been completed for the conterminous United States, using methodology described in SIR 2010-5233, with results provided in three regional reports (PP 1804, PP 1797, and PP 1897), and for Alaska, with results provided in PP 1826.

Hawai'i↗

USGS2014

Temporal variability of carbon and nutrient burial, sediment accretion, and mass accumulation over the past century in a carbonate platform mangrove forest of the Florida Everglades.

The objective of this research was to measure temporal variability in accretion and mass sedimentation rates (including organic carbon (OC), total nitrogen (TN), and total phosphorous (TP)) from the past century in a mangrove forest on the Shark River in Everglades National Park, USA. The 210 Pb Constant Rate of Supply model was applied to six soil cores to calculate annual rates over the most recent 10, 50, and 100 year time spans. Our results show that rates integrated over longer timeframes are lower than those for shorter, recent periods of observation. Additionally, the substantial spatial variability between cores over the 10 year period is diminished over the 100 year record, raising two important implications. First, a multiple-decade assessment of soil accretion and OC burial provides a more conservative estimate and is likely to be most relevant for forecasting these rates relative to long-term processes of sea level rise and climate change mitigation. Second, a small number of sampling locations are better able to account for spatial variability over the longer periods than for the shorter periods. The site average 100 year OC burial rate, 123 ± 19 (standard deviation) g m -2 yr -1 , is low compared with global mangrove values. High TN and TP burial rates in recent decades may lead to increased soil carbon remineralization, contributing to the low carbon burial rates. Finally, the strong correlation between OC burial and accretion across this site signals the substantial contribution of OC to soil building in addition to the ecosystem service of CO 2 sequestration.

Florida↗

USGS1994

Carbonate deposition, Pyramid Lake subbasin, Nevada: 1. Sequence of formation and elevational distribution of carbonate deposits (Tufas)

During the late Quaternary, the elevation of terrace cutting and carbonate deposition in the Pyramid Lake subbasin were controlled by constancy of lake level imposed by spill to adjoining subbasins. Sill elevations are 1177-1183 m (Mud Lake Slough Sill), 1207 m (Emerson Pass Sill), and 1265 m (Darwin Pass Sill). Carbonate deposition was favored by: (1) hydrologic closure, (2) proximity to a source of calcium, (3) elevated water temperature, and (4) a solid substrate. The thickness and aspect of tufa are a function of lake-level dynamics. Relatively thin sheets and pendant sheets were deposited during a rising or falling lake. The upper parts of thick reef-form tufas have a horizontal aspect and were deposited in a lake which was stabilized by spill to the Carson Desert subbasin. The lower parts of the reef-form tufas are thinner and their outer surface has a vertical aspect, indicating that the lower part formed in a receding lake. The thickest and most complete sequences of tufa are mounds that border the Pyramid Lake shore. The tops of the tallest mounds reach the elevation of the Darwin Pass Sill and many mounds have been eroded to the elevations of the Mud Lake Slough Sill of the Emerson Pass Sill. The sequence of tufa formation (from oldest to youngest) displayed in these mounds is: (1) a beachrock containing carbonate-cemented volcanic cobbles, (2) broken and eroded old spheroids that contain thinolitic tufa and an outer rind of dense laminated tufa, (3) large cylindrical (tubular) tufas capped by (4) coatings of old dense tufas, and (5) several generations of old branching tufa commonly associated with thin, platy tufas and coatings of thinolitic tufa, (6) young spheroids that contain poorly oriented young thinolitic tufa in the center and several generations of radially oriented young thinolitic tufas near the outer edge, (7) a transitional thinolite-to-branching tufa, (8) two or more layers of young branching tufa, (9) a 0.5-cm-thick layer of fine-grained dolomite, (10) a 2-cm-thick layer of young dense laminated tufa, (11) a 0.1-cm-thick layer of encrusting tufa that was covered by a beach deposit and (12) a 1.0-cm-thick layer of porous encrusting tufa that coated the beach deposit and the sides of tufa mounds. The elevational ranges of the principal varieties of tufa are not related to terrace or spill elevations. It seems likely that the distribution of tufa varieties is related to variation in the thermal structure or chemistry of Lake Lahontan. It is hypothesized that the thinolitic tufa (ikaite) formed in the near freezing hypolimnion and the braching tufa (calcite) formed in the seasonally warmer epiliminion of the lake.

Nevada↗

USGS2006

Stable carbon isotope depth profiles and soil organic carbon dynamics in the lower Mississippi Basin

Analysis of depth trends of 13C abundance in soil organic matter and of 13C abundance from soil-respired CO2 provides useful indications of the dynamics of the terrestrial carbon cycle and of paleoecological change. We measured depth trends of 13C abundance from cropland and control pairs of soils in the lower Mississippi Basin, as well as the 13C abundance of soil-respired CO2 produced during approximately 1-year soil incubation, to determine the role of several candidate processes on the 13C depth profile of soil organic matter. Depth profiles of 13C from uncultivated control soils show a strong relationship between the natural logarithm of soil organic carbon concentration and its isotopic composition, consistent with a model Rayleigh distillation of 13C in decomposing soil due to kinetic fractionation during decomposition. Laboratory incubations showed that initially respired CO 2 had a relatively constant 13C content, despite large differences in the 13C content of bulk soil organic matter. Initially respired CO2 was consistently 13C-depleted with respect to bulk soil and became increasingly 13C-depleted during 1-year, consistent with the hypothesis of accumulation of 13C in the products of microbial decomposition, but showing increasing decomposition of 13C-depleted stable organic components during decomposition without input of fresh biomass. We use the difference between 13C / 12C ratios (calculated as ??-values) between respired CO 2 and bulk soil organic carbon as an index of the degree of decomposition of soil, showing trends which are consistent with trends of 14C activity, and with results of a two-pooled kinetic decomposition rate model describing CO2 production data recorded during 1 year of incubation. We also observed inconsistencies with the Rayleigh distillation model in paired cropland soils and reasons for these inconsistencies are discussed. ?? 2005 Elsevier B.V. All rights reserved.

Geoderma↗

USGS2002

Black carbon from the Mississippi river: Quantities, sources, and potential implications for the global carbon cycle

Black carbon (BC) may be a major component of riverine carbon exported to the ocean, but its flux from large rivers is unknown. Furthermore, the global distribution of BC between natural and anthropogenic sources remains uncertain. We have determined BC concentrations in suspended sediments of the Mississippi River, the 7th largest river in the world in terms of sediment and water discharge, during high flow and low flow in 1999. The 1999 annual flux of BC from the Mississippi River was 5 × 10 - 4 petagrams (1 Pg = 10 15 g = 1 gigaton). We also applied a principal components analysis to particulate-phase high molecular weight polycyclic aromatic hydrocarbon isomer ratios in Mississippi River suspended sediments. In doing so, we determined that ∼27% of the BC discharged from the Mississippi River in 1999 originated from fossil fuel combustion (coal and smelter-derived combustion), implicating fluvial BC as an important source of anthropogenic BC contamination into the ocean. Using our value for BC flux and the annual estimate for BC burial in ocean sediments, we calculate that, in 1999, the Mississippi River discharged ∼5% of the BC buried annually in the ocean. These results have important implications, not only for the global carbon cycle but also for the fluvial discharge of particulate organic contaminants into the world's oceans.

Louisiana↗

USGS1999

The distribution of, and relation among, mercury and methylmercury, organic carbon, carbonate, nitrogen and phosphorus, in periphyton of the south Florida ecosystem

Periphyton samples from Water Conservation Areas, Big Cypress National Preserve, and Everglades National Park in south Florida were analyzed for concentrations of total mercury, methylmercury, nitrogen, phosphorus, organic carbon, and inorganic carbon. Concentrations of total mercury in periphyton decrease slightly along a gradient from north‐to‐south. Both total mercury and methylmercury are positively correlated with organic carbon, nitrogen and phosphorus in periphyton. In horizontal sections of periphyton mats, total mercury concentrations tend to be largest at the tops and bottoms of the mats. Methylmercury concentrations tend to be the largest near the bottom of mats. These localized elevated concentrations of methylmercury suggest that there are “hot spots”; of methylmercury in periphyton.

Florida↗

USGS2015

Carbon isotope analysis of dissolved organic carbon in fresh and saline (NaCl) water via continuous flow cavity ring-down spectroscopy following wet chemical oxidation

This work examines the performance and limitations of a wet chemical oxidation carbon analyser interfaced with a cavity ring-down spectrometer (WCO-CRDS) in a continuous flow (CF) configuration for measuring δ 13 C of dissolved organic carbon ( δ 13 C-DOC) in natural water samples. Low-chloride matrix (<5 g Cl/L) DOC solutions were analysed with as little as 2.5 mg C/L in a 9 mL aliquot with a precision of 0.5 &permil;. In high-chloride matrix (10–100 g Cl/L) DOC solutions, bias towards lighter δ 13 C-DOC was observed because of incomplete oxidation despite using high-concentration oxidant, extended reaction time, or post-wet chemical oxidation gas-phase combustion. However, through a combination of dilution, chloride removal, and increasing the oxidant:sample ratio, high-salinity samples with sufficient DOC (>22.5 µg C/aliquot) may be analysed. The WCO-CRDS approach requires more total carbon (µg C/aliquot) than conventional CF-isotope ratio mass spectrometer, but is nonetheless applicable to a wide range of DOC concentration and water types, including brackish water, produced water, and basinal brines.

Isotopes in Environmental and Health Studies↗

USGS2009

The changing global carbon cycle: Linking plant-soil carbon dynamics to global consequences

Most current climate-carbon cycle models that include the terrestrial carbon (C) cycle are based on a model developed 40 years ago by Woodwell & Whittaker (1968) and omit advances in biogeochemical understanding since that time. Their model treats net C emissions from ecosystems as the balance between net primary production (NPP) and heterotrophic respiration (HR, i.e. primarily decomposition). Under conditions near steady state, geographic patterns of decomposition closely match those of NPP, and net C emissions are adequately described as a simple balance of NPP and HR (the Woodwell-Whittaker model). This close coupling between NPP and HR occurs largely because of tight coupling between C and N (nitrogen) cycles and because NPP constrains the food available to heterotrophs. Processes in addition to NPP and HR become important to understanding net C emissions from ecosystems under conditions of rapid changes in climate, hydrology, atmospheric CO 2 , land cover, species composition and/or N deposition. Inclusion of these processes in climate-C cycle models would improve their capacity to simulate recent and future climatic change. Processes that appear critical to soil C dynamics but warrant further research before incorporation into ecosystem models include below-ground C flux and its partitioning among roots, mycorrhizas and exudates; microbial community effects on C sequestration; and the effects of temperature and labile C on decomposition. The controls over and consequences of these processes are still unclear at the ecosystem scale. Carbon fluxes in addition to NPP and HR exert strong influences over the climate system under conditions of rapid change. These fluxes include methane release, wildfire, and lateral transfers of food and fibre among ecosystems. Water and energy exchanges are important complements to C cycle feedbacks to the climate system, particularly under non-steady-state conditions. An integrated understanding of multiple ecosystem-climate feedbacks provides a strong foundation for policies to mitigate climate change. Synthesis . Current climate systems models that include only NPP and HR are inadequate under conditions of rapid change. Many of the recent advances in biogeochemical understanding are sufficiently mature to substantially improve representation of ecosystem C dynamics in these models.

Journal of Ecology↗

USGS2011

Development of an assessment methodology for hydrocarbon recovery potential using carbon dioxide and associated carbon sequestration-Workshop findings

The Energy Independence and Security Act of 2007 (Public Law 110-140) authorized the U.S. Geological Survey (USGS) to conduct a national assessment of geologic storage resources for carbon dioxide (CO 2 ) and requested that the USGS estimate the "potential volumes of oil and gas recoverable by injection and sequestration of industrial carbon dioxide in potential sequestration formations" (121 Stat. 1711). The USGS developed a noneconomic, probability-based methodology to assess the Nation's technically assessable geologic storage resources available for sequestration of CO 2 (Brennan and others, 2010) and is currently using the methodology to assess the Nation's CO2 geologic storage resources. Because the USGS has not developed a methodology to assess the potential volumes of technically recoverable hydrocarbons that could be produced by injection and sequestration of CO 2 , the Geologic Carbon Sequestration project initiated an effort in 2010 to develop a methodology for the assessment of the technically recoverable hydrocarbon potential in the sedimentary basins of the United States using enhanced oil recovery (EOR) techniques with CO 2 (CO 2 -EOR). In collaboration with Stanford University, the USGS hosted a 2-day CO 2 -EOR workshop in May 2011, attended by 28 experts from academia, natural resource agencies and laboratories of the Federal Government, State and international geologic surveys, and representatives from the oil and gas industry. The geologic and the reservoir engineering and operations working groups formed during the workshop discussed various aspects of geology, reservoir engineering, and operations to make recommendations for the methodology.

Fact Sheet↗

USGS2021

The importance of wetland carbon dynamics to society: Insight from the Second State of the Carbon Cycle Science Report

The Second State of the Carbon Cycle Report (SOCCR2) culminated in 19 chapters that spanned all North American sectors – from Energy Systems to Agriculture and Land Use – known to be important for understanding carbon (C) cycling and accounting. Wetlands, both inland and coastal, were found to be significant components of C fluxes along the terrestrial to aquatic hydrologic continuum. In this chapter, we synthesize the role of wetlands in the overall C footprint of North America (from Canada to Mexico) as one metric of the societal values placed on these terrestrial-aquatic interfaces. We also summarize the effects of management activities and climate change on the wetland C cycle and give some perspectives on the current and future importance of wetlands to society.

Geophysical Monograph Series↗

USGS2025

Quantifying the effect of petrogenic carbon on SOC turnover for two Rocky Mountain soils: When are petrogenic carbon corrections required?

Petrogenic organic carbon (OC petro ), derived from sedimentary rocks, is an often overlooked and poorly quantified source of soil organic carbon (SOC), which may influence measured or modeled SOC composition, age, and stability. In this study, we exploited differences in thermochemical stability between OC petro and biogenic SOC (OC bio ) using stepped elemental analysis to quantify the fractional contribution of OC petro to total SOC (f petro ), and we conducted a sensitivity analysis to estimate the effects of OC petro on modeled SOC transit times and system ages. Specifically, we compared the effects of accounting for OC petro inputs in SOC turnover modeling (using SoilR) for two montane meadow soils that are underlain by Cretaceous Mancos Shale. At these sites, we estimate that OC petro comprises 7%–9% of the total SOC stock (f petro = 0.07–0.09). However, accounting for OC petro as a mixture of inert and passive C or as completely inert C had negligible effects on SOC transit times and system ages, suggesting that there is a threshold of OC petro content under which there is minimal effect on calculated SOC turnover. Based on our sensitivity analysis, we estimate this threshold to be f petro = 0.125, further supporting that the accurate calculation of OC petro remains an important factor in estimating SOC turnover.

Colorado↗

USGS2016

Potential carbon emissions dominated by carbon dioxide from thawed permafrost soils

Increasing temperatures in northern high latitudes are causing permafrost to thaw , making large amounts of previously frozen organic matter vulnerable to microbial decomposition . Permafrost thaw also creates a fragmented landscape of drier and wetter soil conditions that determine the amount and form (carbon dioxide (CO 2 ), or methane (CH 4 )) of carbon (C) released to the atmosphere. The rate and form of C release control the magnitude of the permafrost C feedback, so their relative contribution with a warming climate remains unclear . We quantified the effect of increasing temperature and changes from aerobic to anaerobic soil conditions using 25 soil incubation studies from the permafrost zone. Here we show, using two separate meta-analyses, that a 10 °C increase in incubation temperature increased C release by a factor of 2.0 (95% confidence interval (CI), 1.8 to 2.2). Under aerobic incubation conditions, soils released 3.4 (95% CI, 2.2 to 5.2) times more C than under anaerobic conditions. Even when accounting for the higher heat trapping capacity of CH 4 , soils released 2.3 (95% CI, 1.5 to 3.4) times more C under aerobic conditions. These results imply that permafrost ecosystems thawing under aerobic conditions and releasing CO 2 will strengthen the permafrost C feedback more than waterlogged systems releasing CO 2 and CH 4 for a given amount of C.

Nature Climate Change↗

USGS2010

The effect of fire and permafrost interactions on soil carbon accumulation in an upland black spruce ecosystem of interior Alaska: Implications for post-thaw carbon loss

High‐latitude regions store large amounts of organic carbon (OC) in active‐layer soils and permafrost, accounting for nearly half of the global belowground OC pool. In the boreal region, recent warming has promoted changes in the fire regime, which may exacerbate rates of permafrost thaw and alter soil OC dynamics in both organic and mineral soil. We examined how interactions between fire and permafrost govern rates of soil OC accumulation in organic horizons, mineral soil of the active layer, and near‐surface permafrost in a black spruce ecosystem of interior Alaska. To estimate OC accumulation rates, we used chronosequence, radiocarbon, and modeling approaches. We also developed a simple model to track long‐term changes in soil OC stocks over past fire cycles and to evaluate the response of OC stocks to future changes in the fire regime. Our chronosequence and radiocarbon data indicate that OC turnover varies with soil depth, with fastest turnover occurring in shallow organic horizons (∼60 years) and slowest turnover in near‐surface permafrost (>3000 years). Modeling analysis indicates that OC accumulation in organic horizons was strongly governed by carbon losses via combustion and burial of charred remains in deep organic horizons. OC accumulation in mineral soil was influenced by active layer depth, which determined the proportion of mineral OC in a thawed or frozen state and thus, determined loss rates via decomposition. Our model results suggest that future changes in fire regime will result in substantial reductions in OC stocks, largely from the deep organic horizon. Additional OC losses will result from fire‐induced thawing of near‐surface permafrost. From these findings, we conclude that the vulnerability of deep OC stocks to future warming is closely linked to the sensitivity of permafrost to wildfire disturbance.

Alaska↗

USGS1970

Water, hydrogen, deuterium, carbon, carbon-13, and oxygen-18 content of selected lunar material

The water content of the breccia is 150 to 455 ppm, with a δD from—580 to —870 per mil. Hydrogen gas content is 40 to 53 ppm with a δD of —830 to —970 per mil. The CO 2 is 290 to 418 ppm with δ 13 C = + 2.3 to + 5.1 per mil and δ 18 O = 14.2 to 19.1 per mil. Non-CO 2 carbon is 22 to 100 ppm, δ 13 C = —6.4 to —23.2 per mil. Lunar dust is 810 ppm H 2 O (D = 80 ppm) and 188 ppm total carbon(δ 13 C = —17.6 per mil). The 18 O analyses of whole rocks range from 5.8 to 6.2 per mil. The temperature of crystallization of type B rocks is 1100° to 1300°C, based on the oxygen isotope fractionation between coexisting plagioclase and ilmenite.

Science↗

USGS1991

High-energy carbonate-sand accumulation, the Quicksands, southwest Florida Keys

High-resolution seismic-reflection profiles of the Quicksands, located along a broad ridge on the platform shelf west of Key West, Florida, indicate a significant deposit of non-oolitic carbonate sand occurs in a belt 47 km long by 28 km wide. The surface of the belt is ornamented by large (5 m), migrating tidal bars, oriented in a north-south direction, on which sand waves, oriented in an east-west direction, are superimposed. Some of the sand waves are awash at low tide. The sand waves are formed by strong reversing tidal currents flowing between the Gulf of Mexico and the Straits of Florida. The waves migrate directly over Pleistocene bedrock to the east, but the deposit thickens to the west and sand waves there overlie non-oolitic Holocene accumulations as thick as 12 m. Westward-dipping accretionary bedding indicates that net migration of the sands is to the west, despite north-south movement of tidal currents. The westward edge of the accumulation has accreted over deeper, muddier deposits. Although tidal currents and resultant bedforms appear identical to those of active ooid deposits in the Bahamas and elsewhere, no oolitically coated grains were found in this study. Thin-section analyses show the principal component (average 48%) of the sands is fragmented plates of species of the green alga Halimeda , followed by particulate coral (average 17%), which increases off the flanks of the main sand body. Short vibracores confirm the presence of cross-bedding.

Florida↗

USGS2020

Modeling geologic sequestration of carbon dioxide in a deep saline carbonate reservoir with TOUGH2–ChemPlugin, a new tool for reactive transport modeling

This paper outlines the development and demonstration of a new tool, TOUGH2–ChemPlugin (T2CPI) for predicting rock–water–CO 2 interaction following injection of supercritical CO 2 into a heterogeneous carbonate system. Specifically, modeling capabilities of TOUGH2, which examines multiphase flow and supercritical CO 2 behavior, were combined with the geochemical modeling capabilities of The Geochemist’s Workbench ® (GWB), using ChemPlugin TM . ChemPlugin is a self-linking re-entrant software object that, when coupled to a transport simulator, retains the flow and transport capabilities of the simulator but enables incorporation of reactive chemistry via GWB. To test and assess the capabilities of T2CPI, results from T2CPI simulations were compared to those of TOUGHREACT, using the same carbonate reservoir parameters (based on the Dollar Bay Formation of the South Florida Basin). Overall, results of simulations from TOUGHREACT and T2CPI were very similar for nearly all evaluated parameters. Dissimilarities between the two programs included qualitative differences in how TOUGHREACT and T2CPI predicted calcite dissolution and the subsequent spatial pattern of the porosity gain caused by how each handles evaporation of water near the injection point. The TOUGHREACT program is a proven, widely used tool for evaluating CO 2 –brine–rock interaction following supercritical CO 2 injection. The T2CPI tool offers similar capabilities and strengths of TOUGHREACT, with the ability to read in and use databases for a wide range of activity coefficient types. This program also has abilities to use a wide range of kinetic constraints, define those kinetic constraints with scripts or compiled libraries, account for colloidal transport, and/or account for a wide range of surface sorption models.

Florida↗