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USGS2025

Where to restore and conserve? A regional benefit cost analysis of coral reef protection and restoration for coastal flood resilience

Momentum is growing for the management of coral reefs as a strategy to reduce climate risks in tropical coastlines. Yet, quantification of the life-time costs, impacts, and benefits remains limited. This study provides one of the first rigorous, spatially explicit, regional-scale Benefit:Cost Analyses (BCA) for coral reef restoration and was designed to meet the BCA requirements of major hazard mitigation funding and programs. This study simulates coastal flooding using a hydrodynamic model under different scenarios representing current coral reef conditions, reef degradation, and reef restoration. These coastal flood maps are used to estimate socioeconomic damages, which are included in a BCA to assess cost-effectiveness and priority areas for coral reef conservation and restoration. The United States Virgin Islands is used as a case study given recent impacts from storms and their new policy that declares reefs as natural infrastructure. The results show that flood risk across the islands of Saint Croix, Saint John, and Saint Thomas is $51.4 million USD per year. Annually, coral reefs prevent flood damages to 481 people and $43.6 million USD of infrastructure, which represents 87 % of the flood risk. These results identify the communities that could receive the greatest benefits from coral conservation and restoration, which overlap significantly. Coral reef restoration is found to be a cost-effective strategy for flood mitigation although how reefs are restored matters. Hybrid coral reef restoration provides greater flood mitigation benefits than ecological restoration, but its cost-effectiveness is overall lower given its greater costs. Many coastal areas have benefit:cost ratios exceeding 1.5, which complies with typical government agencies’ requirements for accessing hazard mitigation funds. This valuation framework helps provide rigorous regional-scale quantification of nature-based coastal protection solutions for coastal risk management decisions.

Journal of Environmental Management↗

USGS2025

Integrating refugia modeling and decision science to support climate-adaptive conservation in the Sierra Nevada

To reduce detrimental impacts of anthropogenic change, natural resource managers often look for place-based solutions to minimize biodiversity loss. Climate-change refugia, areas buffered from contemporary climate change, can enable the persistence of valued natural resources and prolong the benefits of conservation action. Here we combine climate-change refugia modeling with structured decision-making to inform conservation decisions for the endangered foothill yellow-legged frog ( Rana boylii ) in the Sierra Nevada region of California, USA. We used an ensemble of species distribution models to identify areas projected to remain suitable into the 2040s and the 2080s under an RCP 8.5 emissions scenario, as well as areas projected to transition to suitable habitat during this time. We integrated these projections with a structured decision-making process to align management strategies with refugia model outcomes for R. boylii in a subset of the study area. Habitat suitability for R. boylii is projected to decline in the study area by over 90% by the 2040s and by a subsequent 15% by the 2080s. Climate-change refugia are projected to occupy ~7% of present-day suitable habitat, with high agreement between GCMs and model timesteps. Areas projected to transition to suitable habitat within the existing R. boylii clade boundaries are negligible. Collectively, climate-change refugia modeling and structured decision-making provide opportunities to improve resource allocation and empower conservation practitioners in climate change adaptation for at-risk species.

California↗

USGS2025

Methodology for quantifying biodiversity

Protected and Conserved Areas (PCAs) are usually created and managed for multiple values, with biodiversity conservation being the primary value for most PCAs (see Chapter 1). When using Natural Climate Solutions (NCS) or Ecosystem-based Management (EBM) approaches to climate change mitigation, it is important to ensure that there are no unintended negative consequences on biodiversity and co-benefits for biodiversity are sought. This requires baseline biodiversity information and periodic monitoring. The Convention on Biological Diversity (CBD) has developed a monitoring framework to measure progress (CBD COP 15 2022) towards the GBF. The framework consists of: • headline indicators for national, regional and global monitoring; • global level indicators (collated from yes/no responses in national reports and used to provide a count of the number of countries having undertaken specific activities); • component indicators (which are a list of optional indicators that may apply at global, regional, national and sub-national levels); • complementary indicators (which are a list of optional indicators for thematic or in-depth analysis of each goal and target). Further details of the monitoring framework can be found in Decision 15/5: Monitoring framework for the Kunming-Montreal Global Biodiversity Framework (CBD COP 15, 2022). See Table 5.1 for headline indicators and related targets that they measure. These indicators are used to track national progress towards the GBF. However, those designing sub-national or regional PCA frameworks can use them as well. Biodiversity can be measured at different scales, both spatially and temporally, and at different levels and attributes of biological organisation (Noss, 1990). The Kunming-Montreal Global Biodiversity Framework (GBF) (Convention on Biological Diversity, 2022, December 18) includes goals and targets across scales, with Targets 1 and 3 focused on spatial planning and PCA creation, Targets 2 and 4 focused on restoration and species management to prevent extinction, Target 5 focused on fish stocks, Target 8 on minimising climate change impacts, Target 11 on ecosystem services, and Target 21 on biodiversity information for monitoring the GBF.

IUCN WCPA Protected Area Technical Report Series↗

USGS1999

The effect of temperature on experimental and natural chemical weathering rates of granitoid rocks

The effects of climatic temperature variations (5-35??C) on chemical weathering are investigated both experimentally using flow-through columns containing fresh and weathered granitoid rocks and for natural granitoid weathering in watersheds based on annual solute discharge. Although experimental Na and Si effluent concentrations are significantly higher in the fresh relative to the weathered granitoids, the proportional increases in concentration with increasing temperature are similar. Si and Na exhibit comparable average apparent activation energies (E(a)) of 56 and 61 kJ/mol, respectively, which are similar to those reported for experimental feldspar dissolution measured over larger temperature ranges. A coupled temperature-precipitation model, using an expanded database for solute discharge fluxes from a global distribution of 86 granitoid watersheds, produces an apparent activation energy for Si (51 kJ/mol), which is also comparable to those derived from the experimental study. This correlation reinforces evidence that temperature does significantly impact natural silicate weathering rates. Effluent K concentrations in the column study are elevated with respect to other cations compared to watershed discharge due to the rapid oxidation/dissolution of biotite. K concentrations are less sensitive to temperature, resulting in a lower average E(a) value (27 kJ/mol) indicative of K loss from lower energy interlayer sites in biotite. At lower temperatures, initial cation release from biotite is significantly faster than cation release from plagioclase. This agrees with reported higher K/Na ratios in cold glacial watersheds relative to warmer temperate environments. Increased release of less radiogenic Sr from plagioclase relative to biotite at increasing temperature produces corresponding decreases in 87Sr/86Sr ratios in the column effluents. A simple mixing calculation using effluent K/Na ratios, Sr concentrations and 87Sr/86Sr ratios for biotite and plagioclase approximates stoichiometric cation ratios from biotite/plagioclase dissolution at warmer temperatures (35??C), but progressively overestimates the relative proportion of biotite with decreasing temperature. Ca, Mg, and Sr concentrations closely correlate, exhibit no consistent trends with temperature, and are controlled by trace amounts of calcite or exchange within weathered biotite. The inability of the watershed model to differentiate a climate signal for such species correlates with the lower temperature dependence observed in the experimental studies.

Geochimica et Cosmochimica Acta↗

USGS2021

Weathering of slags

Weathering is a natural process causing the transformation of minerals, rocks, and related materials like glass under near-surface conditions. Although metallurgical slags are human-made materials, they also undergo natural weathering processes. As base metal slags weather, the released solutions may contain contaminants that could pose an environmental risk. On the other hand, weathering of ferrous slags is important because of the common reuse of the slags. This chapter summarizes factors that affect rates of slag weathering as well as defining and characterizing the two stages of weathering (incipient and advanced) as they are observed in a wide variety of individual phases and slags. We conclude that slags weather at different scales and rates depending on their chemistry and phase composition as well as the external conditions. Furthermore, weathering of slags is a process that is not perfectly reflected by natural processes because these materials are complex (in terms of texture, composition, and disequilibrium with surficial conditions) and not always analogous to rocks. Therefore, some information in this chapter on weathering is applicable to all slag types, some is relevant to only specific slag types, and some aspects require additional study.

Book chapter↗

USGS1976

Magnitude and frequency of floods in Nebraska

Estimates of flood characteristics with recurrence intervals up to 100 years can be obtained at most sites in Nebraska by use of techniques presented in this report. Instructions, equations, and graphs are presented to aid the design engineer in estimating the magnitude and frequency of floods. For natural-flow streams, the estimating equations and graphical solutions are based on regional relations between floods of a specific return period and selected basin characteristics. Nebraska was subdivided into five hydrologic regions by means of regressions and residuals from the regressions. The boundaries of Regions 1 and 2 were determined to a great extent by differences in soil type. The divisions between Region 2 and Region 4 were also determined by differences in soil type. Boundaries of Region 3 and Region 5 are along or near basin divides. Flood magnitude and frequency solution diagrams are presented for major controlled streams such as the North Platte, South Platte, Platte, and Republican Rivers. Flood information on small controlled streams is limited to available station data. Flood characteristics are tabulated for 303 gaging stations having 13 or more years of record. These flood characteristics provide the best information on floods at these gaged sites. Observed maximum flood peaks at 303 gaging stations with 13 or more years of record and significant peaks at 57 short-term stations and 31 miscellaneous sites are useful in designing flood-control works for maximum safety from flood damage. Comparison is made with maximum observed floods in the United States.

Nebraska↗

USGS1986

The SALT NORM : a quantitative chemical-mineralogical characterization of natural waters

The new computer program SNORM calculates the salt norm from the chemical composition of a natural water. The salt norm is the quantitative ideal equilibrium assemblage that would crystallize if the water evaporated to dryness at 25 C and 1 bar pressure under atmospheric partial pressure of CO2. SNORM proportions solute concentrations to achieve charge balance. It quantitatively distributes the 18 acceptable solutes into normative salts that are assigned from 63 possible normative salts to allow only stable associations based on the Gibbs Phase Rule, available free energy values, and observed low-temperature mineral associations. Although most natural water compositions represent multiple solute origins, results from SNORM identify three major categories: meteoric or weathering waters that are characterized by normative alkali-bearing sulfate and carbonate salts: connate marine-like waters that are chloride-rich with a halite-bischofite-carnallite-kieserite-anhydrite association; and diagenetic waters that are frequently of marine origin but yield normative salts, such as Ca-bearing chlorides (antarcticite and tachyhydrite) and sylvite, which suggest solute alteration by secondary mineral reactions. The solute source or reaction process within each of the above categories is commonly indicated by the presence or absence of diagnostic normative salts and their relative abundance in the normative salt assemblage. For example, salt norms: (1) may identify lithologic source; (2) may identify the relative roles of carbonic and sulfuric acid hydrolysis in the evolution of weathering waters; (3) may identify the origin of connate water from normal marine, hypersaline, or evaporite salt resolution processes; and (4) may distinguish between dolomitization and silicate hydrolysis or exchange for the origin of diagenetic waters. (Author 's abstract)

Water-Resources Investigations Report↗

USGS2014

Nonsteady flow to a well of constant drawdown in an extensive aquifer

A mathematical theory is given for the discharge of a well of constant drawdown, discharging as by natural flow from an effectively infinite aquifer of uniform transmissibility and uniform compressibility. This theory is based on the solution by L. P. Smith of the analogous problem in heat conduction. The mathematical function involved in the solution, which cannot be integrated directly, is evaluated by numerical integration. A table of its values is given for a wide range of its argument. This function is compared with other,asymptotic solutions, and simple, useful approximations are given. Two graphical methods are outlined for determining the coefficients of storage and transmissibility from variations in the rate of discharge of wells flowing at constant drawdown. Data from the Grand Junction, Colo., artesian basin are treated by these methods. In the Grand Junction artesian basin there are about 25 flowing wells ranging in depth from 600 to 1600 ft, most of which obtain water from the Entrada sandstone. A few of the wells obtain water from a sandstone in the overlying Morrison formation and a few tap the underlying Wingate sandstone. The procedure of the tests is outlined, and the “ink-well” mercury gage used to measure the artesian pressures is described. Recovery tests were run on the same wells after the discharge tests. Values of transmissibility obtained from the recovery tests check those obtained by means of the discharge tests.

Colorado↗

USGS1984

Development of a model to predict the adsorption of lead from solution on a natural streambed sediment

Adsorption of solutes by solid mineral surfaces commonly influences the dissolved ionic composition of natural waters. A model based on electrical double-layer theory has been developed which appears to be capable of characterizing the surface chemical behavior of a natural fine-grained sediment containing mostly quartz and feldspar. This variable surface charge-variable surface potential (VSC-VSP) model differs from others in being capable of evaluating more closely the effect of total metal ion activity on the pH-dependent change in electrical potential at the solid surface. The model was tested using 10-4 molar solutions of lead and a silt-size fraction of sediment from the bed of Colma Creek, a small stream in urban northern San Mateo County, California. The average deviation of measured percent adsorption and values calculated from the model was 6.6 adsorption percent from pH 2.0 to pH 7.0.

Water Supply Paper↗

USGS1976

Classification of organic solutes in water by using macroreticular resins

A series of macroreticular resin adsorbents was evaluated for ability to extract and fractionate organic solutes found in natural waters. Studies with organic solute standards and natural water samples lead to the development of dissolved organic carbon (DOC) fractionation analysis whereby the DOC is concentrated and fractionated by macroreticular resins into acid, base, and neutral hydrophobic organic solute fractions and into acid, base, and neutral hydrophilic organic solute fractions. The hydrophobic solutes were sorbed and fractionated on nonionic, nonpolar macroreticular resins, and the hydrophilic solutes were sorbed and fractionated by macroreticular ion-exchange resins. Organic-inorganic complexes as well as organic solutes were isolated by resin sorption. DOC fractionation analysis was developed to serve as a compound classification that fills the gap in organic solute characterization between the organic solute concentration (DOC) and specific compound identification.

Journal of Research of the U.S. Geological Survey↗

USGS2011

A distribution-based parameterization for improved tomographic imaging of solute plumes

Difference geophysical tomography (e.g. radar, resistivity and seismic) is used increasingly for imaging fluid flow and mass transport associated with natural and engineered hydrologic phenomena, including tracer experiments, in situ remediation and aquifer storage and recovery. Tomographic data are collected over time, inverted and differenced against a background image to produce ‘snapshots’ revealing changes to the system; these snapshots readily provide qualitative information on the location and morphology of plumes of injected tracer, remedial amendment or stored water. In principle, geometric moments (i.e. total mass, centres of mass, spread, etc.) calculated from difference tomograms can provide further quantitative insight into the rates of advection, dispersion and mass transfer; however, recent work has shown that moments calculated from tomograms are commonly biased, as they are strongly affected by the subjective choice of regularization criteria. Conventional approaches to regularization (Tikhonov) and parametrization (image pixels) result in tomograms which are subject to artefacts such as smearing or pixel estimates taking on the sign opposite to that expected for the plume under study. Here, we demonstrate a novel parametrization for imaging plumes associated with hydrologic phenomena. Capitalizing on the mathematical analogy between moment-based descriptors of plumes and the moment-based parameters of probability distributions, we design an inverse problem that (1) is overdetermined and computationally efficient because the image is described by only a few parameters, (2) produces tomograms consistent with expected plume behaviour (e.g. changes of one sign relative to the background image), (3) yields parameter estimates that are readily interpreted for plume morphology and offer direct insight into hydrologic processes and (4) requires comparatively few data to achieve reasonable model estimates. We demonstrate the approach in a series of numerical examples based on straight-ray difference-attenuation radar monitoring of the transport of an ionic tracer, and show that the methodology outlined here is particularly effective when limited data are available.

Geophysical Journal International↗

USGS2000

An assessment of calcite crystal growth mechanisms based on crystal size distributions

Calcite crystal growth experiments were undertaken to test a recently proposed model that relates crystal growth mechanisms to the shapes of crystal size distributions (CSDs). According to this approach, CSDs for minerals have three basic shapes: (1) asymptotic, which is related to a crystal growth mechanism having constant-rate nucleation accompanied by surface-controlled growth; (2) lognormal, which results from decaying-rate nucleation accompanied by surface-controlled growth; and (3) a theoretical, universal, steady-state curve attributed to Ostwald ripening. In addition, there is a fourth crystal growth mechanism that does not have a specific CSD shape, but which preserves the relative shapes of previously formed CSDs. This mechanism is attributed to supply-controlled growth. All three shapes were produced experimentally in the calcite growth experiments by modifying nucleation conditions and solution concentrations. The asymptotic CSD formed when additional reactants were added stepwise to the surface of solutions that were supersaturated with respect to calcite (initial Ω = 20, where Ω = 1 represents saturation), thereby leading to the continuous nucleation and growth of calcite crystals. Lognormal CSDs resulted when reactants were added continuously below the solution surface, via a submerged tube, to similarly supersaturated solutions (initial Ω = 22 to 41), thereby leading to a single nucleation event followed by surface-controlled growth. The Ostwald CSD resulted when concentrated reactants were rapidly mixed, leading initially to high levels of supersaturation (Ω >100), and to the formation and subsequent dissolution of very small nuclei, thereby yielding CSDs having small crystal size variances. The three CSD shapes likely were produced early in the crystallization process, in the nanometer crystal size range, and preserved during subsequent growth. Preservation of the relative shapes of the CSDs indicates that a supply-controlled growth mechanism was established and maintained during the constant-composition experiments. CSDs having shapes intermediate between lognormal and Ostwald also were generated by varying the initial levels of supersaturation (initial Ω = 28.2 to 69.2) in rapidly mixed solutions. Lognormal CSDs were observed for natural calcite crystals that are found in septarian concretions occurring in southeastern Colorado. Based on the model described above, these CSDs indicate initial growth by surface control, followed by supply-controlled growth. Thus, CSDs may be used to deduce crystal growth mechanisms from which geologic conditions early in the growth history of a mineral can be inferred. Conversely, CSD shape can be predicted during industrial crystallization by applying the appropriate conditions for a particular growth mechanism.

Geochimica et Cosmochimica Acta↗

USGS1985

Chemistry and transport of soluble humic substances in forested watersheds of the Adirondack Park, New York

Studies were conducted in conjunction with the Integrated Lake-Watershed Acidification Study (ILWAS) to examine the chemistry and leaching patterns of soluble humic substances in forested watersheds of the Adirondack region. During the summer growing season, mean dissolved organic carbon (DOC) concentrations in the ILWAS watersheds ranged from 21–32 mg C l −1 in O/A horizon leachates, from 5–7 mg C l −1 in B horizon leachates, from 2–4 mg C l −1 in groundwater solutions, from 6–8 mg C l −1 in first order streams, from 3–8 mg C l −1 in lake inlets, and from 2–7 mg C l −1 in lake outlets. During the winter, mean DOC concentrations dropped significantly in the upper soil profile. Soil solutions from mixed and coniferous stands contained as much as twice the DOC concentration of lysimeter samples from hardwood stands. Results of DOC fractionation analysis showed that hydrophobia and hydrophilic acids dominate the organic solute composition of natural waters in these watersheds. Charge balance and titration results indicated that the general acid-base characteristics of the dissolved humic mixture in these natural waters can be accounted for by a model organic acid having an average p K a of 3.85, an average charge density of 4–5 μeq mg −1 C at ambient pH, and a total of 6–7 meq COOH per gram carbon.

New York↗

USGS2007

The NatCarb geoportal: Linking distributed data from the Carbon Sequestration Regional Partnerships

The Department of Energy (DOE) Carbon Sequestration Regional Partnerships are generating the data for a "carbon atlas" of key geospatial data (carbon sources, potential sinks, etc.) required for rapid implementation of carbon sequestration on a broad scale. The NATional CARBon Sequestration Database and Geographic Information System (NatCarb) provides Web-based, nation-wide data access. Distributed computing solutions link partnerships and other publicly accessible repositories of geological, geophysical, natural resource, infrastructure, and environmental data. Data are maintained and enhanced locally, but assembled and accessed through a single geoportal. NatCarb, as a first attempt at a national carbon cyberinfrastructure (NCCI), assembles the data required to address technical and policy challenges of carbon capture and storage. We present a path forward to design and implement a comprehensive and successful NCCI. ?? 2007 The Haworth Press, Inc. All rights reserved.

Journal of Map & Geography Libraries↗

USGS1995

Soil-solution chemistry in a low-elevation spruce-fir ecosystem, Howland, Maine

Soil solutions were collected monthly by tension and zero-tension lysimeters in a low-elevation red spruce stand in east-central Maine from May 1987 through December 1992. Soil solutions collected by Oa tension lysimeters had higher concentrations of most constituents than the Oa zero-tension lysimeters. In Oa horizon soil solutions growing season concentrations for SO 4 , Ca, and Mg averaged 57, 43, and 30 μmol L −1 in tension lysimeters, and 43, 28, and 19 μmol L −1 in zero-tension lysimeters, respectively. Because tension lysimeters remove water held by the soil at tensions up to 10 kPa, solutions are assumed to have more time to react with the soil compared to freely draining solutions collected by zero-tension lysimeters. Solutions collected in the Bs horizon by both types of collectors were similar which was attributed to the frequency of time periods when the water table was above the Bs lysimeters. Concentrations of SO 4 and NO 3 at this site were lower than concentrations reported for most other eastern U.S. spruce-fir sites, but base cation concentrations fell in the same range. Aluminum concentrations in this study were also lower than reported for other sites in the eastern U.S. and Ca/Al ratios did not suggest inhibition of Ca uptake by roots. Concentrations of SO 4 , Ca, K, and Cl decreased significantly in both the Oa and Bs horizons over the 56-month sampling period, which could reflect decreasing deposition rates for sulfur and base cations, climatic influences, or natural variation. A longer record of measured fluxes will be needed to adequately define temporal trends in solution chemistry and their causes.

Maine↗

USGS1968

Activity product constant of cryolite at 25°C and one atmosphere using selective-ion electrodes to estimate sodium and fluoride activities

The activity product constant of cryolite (Na 3 AlF 6 ) at 25°C and 1 atm total pressure was calculated from data for solutions from which synthetic cryolite or mixtures of cryolite and a solid apparently related to ralstonite had precipitated. The activities of fluoride and of sodium were estimated using specific ion electrodes. The activity of Al 3+ was calculated from aluminum concentrations using equations which involve aluminum species existing in water solutions containing fluoride and hydroxide ions. For the reaction Na 3 AlF 6 ( c ) = 3 Na ( aq ) + + Al 3+ ( aq ) + 6 E - ( aq ) the activity product constant K so is 10 −33.84 , and the standard free energy of formation at 25°C is -745.4±1.0 kcal mole −1 . This latter is identical to a value from the literature which is based on calorimetric data. Although cryolite and related minerals are easily precipitated in the laboratory, their relative scarcity in nature suggests that the effect of influences, perhaps solutes other than those occurring in the structure, may inhibit or prevent the formation of cryolite.

Geochimica et Cosmochimica Acta↗

USGS2017

A guide to multi-objective optimization for ecological problems with an application to cackling goose management

Choices in ecological research and management are the result of balancing multiple, often competing, objectives. Multi-objective optimization (MOO) is a formal decision-theoretic framework for solving multiple objective problems. MOO is used extensively in other fields including engineering, economics, and operations research. However, its application for solving ecological problems has been sparse, perhaps due to a lack of widespread understanding. Thus, our objective was to provide an accessible primer on MOO, including a review of methods common in other fields, a review of their application in ecology, and a demonstration to an applied resource management problem. A large class of methods for solving MOO problems can be separated into two strategies: modelling preferences pre-optimization (the a priori strategy), or modelling preferences post-optimization (the a posteriori strategy). The a priori strategy requires describing preferences among objectives without knowledge of how preferences affect the resulting decision. In the a posteriori strategy, the decision maker simultaneously considers a set of solutions (the Pareto optimal set) and makes a choice based on the trade-offs observed in the set. We describe several methods for modelling preferences pre-optimization, including: the bounded objective function method, the lexicographic method, and the weighted-sum method. We discuss modelling preferences post-optimization through examination of the Pareto optimal set. We applied each MOO strategy to the natural resource management problem of selecting a population target for cackling goose ( Branta hutchinsii minima ) abundance. Cackling geese provide food security to Native Alaskan subsistence hunters in the goose's nesting area, but depredate crops on private agricultural fields in wintering areas. We developed objective functions to represent the competing objectives related to the cackling goose population target and identified an optimal solution first using the a priori strategy, and then by examining trade-offs in the Pareto set using the a posteriori strategy. We used four approaches for selecting a final solution within the a posteriori strategy; the most common optimal solution, the most robust optimal solution, and two solutions based on maximizing a restricted portion of the Pareto set. We discuss MOO with respect to natural resource management, but MOO is sufficiently general to cover any ecological problem that contains multiple competing objectives that can be quantified using objective functions.

Ecological Modelling↗

USGS2017

CO2 diffusion into pore spaces limits weathering rate of an experimental basalt landscape

Basalt weathering is a key control over the global carbon cycle, though in situ measurements of carbon cycling are lacking. In an experimental, vegetation-free hillslope containing 330 m 3 of ground basalt scoria, we measured real-time inorganic carbon dynamics within the porous media and seepage flow. The hillslope carbon flux (0.6–5.1 mg C m –2 h –1 ) matched weathering rates of natural basalt landscapes (0.4–8.8 mg C m –2 h –1 ) despite lacking the expected field-based impediments to weathering. After rainfall, a decrease in CO 2 concentration ([CO 2 ]) in pore spaces into solution suggested rapid carbon sequestration but slow reactant supply. Persistent low soil [CO 2 ] implied that diffusion limited CO 2 supply, while when sufficiently dry, reaction product concentrations limited further weathering. Strong influence of diffusion could cause spatial heterogeneity of weathering even in natural settings, implying that modeling studies need to include variable soil [CO 2 ] to improve carbon cycling estimates associated with potential carbon sequestration methods.

Geology↗