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USGS2013

Estimating ecosystem carbon stocks at Redwood National and State Parks

Accounting for ecosystem carbon is increasingly important for park managers. In this case study we present our efforts to estimate carbon stocks and the effects of management on carbon stocks for Redwood National and State Parks in northern California. Using currently available information, we estimate that on average these parks’ soils contain approximately 89 tons of carbon per acre (200 Mg C per ha), while vegetation contains about 130 tons C per acre (300 Mg C per ha). estoration activities at the parks (logging-road removal, second-growth forest management) were shown to initially reduce ecosystem carbon, but may provide for enhanced ecosystem carbon storage over the long term. We highlight currently available tools that could be used to estimate ecosystem carbon at other units of the National Park System.

California↗

USGS2009

Acid neutralizing capacity and leachate results for igneous rocks, with associated carbon contents of derived soils, Animas River AML site, Silverton, Colorado

Mine planning efforts have historically overlooked the possible acid neutralizing capacity (ANC) that local igneous rocks can provide to help neutralize acidmine drainage. As a result, limestone has been traditionally hauled to mine sites for use in neutralizing acid drainage. Local igneous rocks, when used as part of mine life-cycle planning and acid mitigation strategy, may reduce the need to transport limestone to mine sites because these rocks can contain acid neutralizing minerals. Igneous hydrothermal events often introduce moderately altered mineral assemblages peripheral to more intensely altered rocks that host metal-bearing veins and ore bodies. These less altered rocks can contain ANC minerals (calcite-chlorite-epidote) and are referred to as a propylitic assemblage. In addition, the carbon contents of soils in areas of new mining or those areas undergoing restoration have been historically unknown. Soil organic carbon is an important constituent to characterize as a soil recovery benchmark that can be referred to during mine cycle planning and restoration. This study addresses the mineralogy, ANC, and leachate chemistry of propylitic volcanic rocks that host polymetallic mineralization in the Animas River watershed near the historical Silverton, Colorado, mining area. Acid titration tests on volcanic rocks containing calcite (2 – 20 wt %) and chlorite (6 – 25 wt %), have ANC ranging from 4 – 146 kg/ton CaCO3 equivalence. Results from a 6-month duration, kinetic reaction vessel test containing layered pyritic mine waste and underlying ANC volcanic rock (saturated with deionized water) indicate that acid generating mine waste (pH 2.4) has not overwhelmed the ANC of propylitic volcanic rocks (pH 5.8). Sequential leachate laboratory experiments evaluated the concentration of metals liberated during leaching. Leachate concentrations of Cu-Zn-As-Pb for ANC volcanic rock are one-to-three orders of magnitude lower when compared to leached solution from mine waste used in the kinetic reaction vessel test. This finding suggests that mine waste and not ANC rock may generate the majority of leachable metals in a field scenario. The organic carbon content of naturally reclaimed soils derived from weathering of propylitically-altered andesite was determined in catchments where ANC studies were initiated. Soils were found to have total carbon concentrations (TOC) that exceed global average soil TOC abundances by as much as 1.5 – 5 times. These data support an environmental management system involving use of ANC rocks as part of life-cycle mine planning to reduce post-mine closure acid mitigation measures. Carbon contents of undisturbed soils in mined catchments can possibly be used to validate post-reclamation success and help quantify carbon sequestration for CO2 emission offset trading as carbon markets mature.

Colorado↗

USGS2016

The potential carbon benefit of reforesting Hawai‘i Island non-native grasslands with endemic Acacia koa trees

Large areas of forest in the tropics have been cleared and converted to pastureland. Hawai‘i Island is no exception, with over 100,000 ha of historically forested land now dominated by non-native grasses. Passive forest restoration has been unsuccessful because these grasslands tend to persist even after grazers have been removed, yet active outplanting of native tree species can be cost-prohibitive at the landscape scale. It is therefore essential to seek co-benefits of forest restoration to defray costs, such as accredited carbon offsets from increased carbon sequestration. We developed a reforestation scenario for non-native grasslands on Hawai‘i Island by outplanting endemic koa ( Acacia koa ) trees paid for with carbon offsets via the California Cap and Trade Program. This scenario entails reforesting 53,531 ha of non-native grassland at 2500 ha y-1 over 22 years. We estimated planting costs at \$6,178 ha-1, a total cost of approximately \$331,000,000. We used the Land Use and Carbon Simulator (LUCAS) model to estimate island-wide ecosystem carbon sequestration with and without koa reforestation using 100 Monte Carlo simulations per year over a 60-year period. Income from carbon offsets was set at \$13.57 per ton of CO 2 equivalent, the current California Cap and Trade Program carbon market price.

Hawai'i↗

USGS2021

Ecosystem service co-benefits provided through wetland carbon management

What is the role of wetland carbon management in providing ecosystem services? Ecosystem services are the benefits that nature provides to people, and they are often categorized as: provisioning (e.g., food and water), regulating (e.g., climate mitigation and flood protection), cultural (e.g., cultural and recreational), and supporting (e.g., nutrient cycling) services ( www.millenniumassessment.org/ ). Ecosystem services are a function of the quantity and quality of the ecosystem. External factors such as land development, pollution, fragmentation, resource overuse, and climate change can negatively influence an ecosystem's capacity to provide ecosystem services; conversely, management actions to conserve and restore systems can increase ecosystem services (Pindilli, 2019). Wetland carbon management is a set of preservation, conservation, or restoration actions used to preserve ecosystem function that protects or enhances stored carbon or biologic carbon sequestration, with the intent to regulate climate (see Moomaw et al., 2018). By managing for wetland carbon resources, there is often a co-benefit of the preservation or enhancement of other ecosystem services; it may also increase ecosystem disservices (such as mosquito production). This chapter provides an overview of the types of ecosystem service co-benefits provided by wetland carbon management, with specific examples from the literature.

Book chapter↗

USGS2012

Threshold amounts of organic carbon needed to initiate reductive dechlorination in groundwater systems

Aquifer sediment and groundwater chemistry data from 15 Department of Defense facilities located throughout the United States were collected and analyzed with the goal of estimating the amount of natural organic carbon needed to initiate reductive dechlorination in groundwater systems. Aquifer sediments were analyzed for hydroxylamine and NaOH-extractable organic carbon, yielding a probable underestimate of potentially bioavailable organic carbon (PBOC). Aquifer sediments were also analyzed for total organic carbon (TOC) using an elemental combustion analyzer, yielding a probable overestimate of bioavailable carbon. Concentrations of PBOC correlated linearly with TOC with a slope near one. However, concentrations of PBOC were consistently five to ten times lower than TOC. When mean concentrations of dissolved oxygen observed at each site were plotted versus PBOC, it showed that anoxic conditions were initiated at approximately 200 mg/kg of PBOC. Similarly, the accumulation of reductive dechlorination daughter products relative to parent compounds increased at a PBOC concentration of approximately 200 mg/kg. Concentrations of total hydrolysable amino acids (THAA) in sediments also increased at approximately 200 mg/kg, and bioassays showed that sediment CO 2 production correlated positively with THAA. The results of this study provide an estimate for threshold amounts of bioavailable carbon present in aquifer sediments (approximately 200 mg/kg of PBOC; approximately 1,000 to 2,000 mg/kg of TOC) needed to support reductive dechlorination in groundwater systems.

Remediation Journal↗

USGS2017

Paleoclimatic reconstruction using the correlation in δ 18 O of hackberry carbonate and environmental water, North America

Celtis sp. (commonly known as “hackberry”) fruits were collected from 101 North American sites located in 13 states and one Canadian province between the years of 1979–1994. The biomineralized carbonate endocarp of the hackberry, which is a common botanical fossil found throughout the Quaternary sediments of the Great Plains, was analyzed for its δ 18 O value and plotted against the δ 18 O value of site environmental water to demonstrate the potential of the hackberry as a paleoclimate indicator. This correlation was reinforced by intensive studies on extracted tissue-water δ 18 O value and hackberry endocarp carbonate δ 18 O value from three trees in Sterling, Colorado. The observed correlation in the large data set between hackberry endocarp carbonate δ 18 O value and environmental water is [endocarp δ 18 O=38.56+0.69×environmental water δ 18 O] ( R =0.88; R 2 =0.78; p value<0.0001). The relation of the hackberry carbonate to temperature in the Great Plains was the following: (average daily-maximum growing season temperature [°C])=6.33+0.67 (δ 18 O of endocarp carbonate) ( R =0.73; R 2 =0.54; p value=0.0133). The δ 18 O value of early Holocene fossil hackberry carbonate in the Pintwater Cave, southern Nevada, suggested precipitation δ 18 O values more positive than today (&sim;−4&permil; early Holocene vs &sim;−9 to −10&permil; today). This shift, combined with paleobotanical data, suggests an influx of summer monsoonal moisture to this region in the early Holocene. Alternatively, the more positive δ 18 O values could be viewed as suggestive of warmer temperatures, although the direct use of Great Plains hackberry/temperature relationships to the Great Basin is of debatable value.

Quaternary Research↗

USGS2014

Radiocarbon dating of terrestrial carbonates

Terrestrial carbonates encompass a wide range of materials that potentially could be used for radiocarbon ( 14 C) dating. Biogenic carbonates, including shells and tests of terrestrial and aquatic gastropods, bivalves, ostracodes, and foraminifera, are preserved in a variety of late Quaternary deposits and may be suitable for 14C dating. Primary calcareous deposits (marls, tufa, speleothems) and secondary carbonates (rhizoliths, fracture fill, soil carbonate) may also be targeted for dating when conditions are favorable. This chapter discusses issues that are commonly encountered in 14 C dating of terrestrial carbonates, including isotopic disequilibrium and open-system behavior, as well as methods used to determine the reliability of ages derived from these materials. Recent methodological advancements that may improve the accuracy and precision of 14 C ages of terrestrial carbonates are also highlighted.

Book chapter↗

USGS1980

Stable isotope and fluid inclusion studies of carbonate deposits from the Tolfa Mountains mining district (Latium, central Italy)

Carbon and oxygen isotope analyses were made of representative samples of calcite and quartz from the carbonate deposits in the Tolfa Mountains mining district. Measurements were also made of hydrogen isotope compositions, filling temperatures and salinities of fluid inclusions in these minerals. There are three stages of mineralization at Tolfa. In stage I, characterized by calc-silicate hornfels, the carbonates have relatively high ?? 18O values of 14.5 to 21.6 suggesting a rather low water/rock ratio. ??13C values of -0.3 to 2.1 indicate that appreciable decarbonation or introduction of deep-seated carbon did not occur. Stage II is marked by phanerocrystalline carbonates; ?? 18O values of 13.1 to 20.0 and ??13C values of 0.7 to 5.0 identify them as hydrothermal veins rather than marbles. ?? D values of -56 to -50 for inclusion fluids suggest a possible magmatic component to the hydrothermal fluid. Filling temperatures of coarse-grained samples of Calcite II are 309?? to 362?? C with a salinity range of 5.3 to 7.1 weight percent NaCl. Calculated ??18O values of 11-12 for these fluids are again indicative of low water/rock ratios. The sparry calcites of stage III have ??18O and ??13C values of 8.1 to 12.9 and -1.7 to 3.2, respectively. ?? D values of inclusion fluids are -40 to -33, clearly heavier than in earlier stages and similar to values of modern local ground waters. A salinity measurement of <0.1 weight percent NaCl in a sample of Calcite III is compatible with a relatively unaltered ground water origin for this fluid. Precipitation of the sparry calcite took place at much lower temperatures, around 160?? C. For quartz, ??18O values of 9.3 to 12.4 and ?? D values for inclusions of -53 to -28 are consistent with its late occurrence and paragenetic link with associated carbonates. ?? 1980 Springer-Verlag.

Mineralium Deposita↗

USGS2006

Reconciling carbon-cycle concepts, terminology, and methods

Recent projections of climatic change have focused a great deal of scientific and public attention on patterns of carbon (C) cycling as well as its controls, particularly the factors that determine whether an ecosystem is a net source or sink of atmospheric carbon dioxide (CO 2 ). Net ecosystem production (NEP), a central concept in C-cycling research, has been used by scientists to represent two different concepts. We propose that NEP be restricted to just one of its two original definitions—the imbalance between gross primary production (GPP) and ecosystem respiration (ER). We further propose that a new term—net ecosystem carbon balance (NECB)—be applied to the net rate of C accumulation in (or loss from [negative sign]) ecosystems. Net ecosystem carbon balance differs from NEP when C fluxes other than C fixation and respiration occur, or when inorganic C enters or leaves in dissolved form. These fluxes include the leaching loss or lateral transfer of C from the ecosystem; the emission of volatile organic C, methane, and carbon monoxide; and the release of soot and CO 2 from fire. Carbon fluxes in addition to NEP are particularly important determinants of NECB over long time scales. However, even over short time scales, they are important in ecosystems such as streams, estuaries, wetlands, and cities. Recent technological advances have led to a diversity of approaches to the measurement of C fluxes at different temporal and spatial scales. These approaches frequently capture different components of NEP or NECB and can therefore be compared across scales only by carefully specifying the fluxes included in the measurements. By explicitly identifying the fluxes that comprise NECB and other components of the C cycle, such as net ecosystem exchange (NEE) and net biome production (NBP), we can provide a less ambiguous framework for understanding and communicating recent changes in the global C cycle.

Ecosystems↗

USGS2018

Fire changes the spatial distribution and sources of soil organic carbon in a grassland-shrubland transition zone

Aims In many mixed grass-shrub ecosystems, increased shrub biomass tends to promote overall carbon storage, but the distribution of carbon pools may be complicated by disturbances such as wildfires. We investigated the spatial distribution of surface soil organic carbon (SOC) and its relative contribution from grasses and shrubs after fires in a grass-shrub transition zone in the northern Chihuahuan Desert, USA. Methods We used a prescribed fire to create a burned treatment, then collected soil and plant samples. The biogeochemical approaches, geostatistical analyses, and carbon partitioning analyses were used to quantify the SOC and soil δ 13 C spatial patterns. Results Before the prescribed fire, up to 98% of the spatial dependence of SOC was autocorrelated at a distance of 1.91 m, corresponding to the approximate average shrub canopy diameter, but the spatial dependence dropped to 81% at a larger autocorrelation distance (3.74 m) two windy seasons after the fire. C 4 grasses and C 3 shrubs contributed approximately equal amounts of carbon to the surface SOC pool before the prescribed fire. However, C 4 grasses became the dominant source of SOC two windy seasons following the fire. For individual microsites, a substantially increased proportion of SOC was derived from C 4 grasses at the shrub microsites following the fire. Conclusions The higher proportion of C 4 grasses-derived SOC at the shrub microsites post-fire suggests that SOC may have preferred pathways to move among different microsites following fire disturbance. The distinct spatial distribution patterns of δ 13 C, and the increased contribution of SOC from grasses may be explained by the rapid recovery of grasses following the fire. Overall, our results provide insights into how fire might be used as a management tool to alter soil carbon pools in the context of shrub encroachment.

Plant and Soil↗

USGS2020

Structural impacts, carbon losses, and regeneration in mangrove wetlands after two hurricanes on St. John, U.S. Virgin Islands

Hurricanes Irma and Maria ravaged the mangroves of St. John, U.S. Virgin Islands, in 2017. Basal area losses were large (63–100%) and storm losses of carbon associated with aboveground biomass amounted to 11.9–43.5 Mg C/ha. Carbon biomass of dead standing trees increased 8.1–18.3 Mg C/ha among sites, and carbon in coarse woody debris on the forest floor increased 1.9–18.2 Mg C/ha, with effects varying by mangrove typology. While St. John has only ~45 ha of mangroves, they exist as isolated basins, salt ponds, and fringe mangroves; the latter sometimes support diverse marine communities. Salt pond and fringe mangroves had proportionately more organic carbon (46.3 Mg C/ha) than inorganic carbon (1.1 Mg C/ha) in soils than isolated basins. Soil organic carbon was also appreciable in isolated basins (30.8 Mg C/ha) but was matched by inorganic C (36.7 Mg C/ha), possibly due to adjacent land use history (e.g., road construction), previous storm overwash, or geomorphology. Soil nitrogen stocks were low across all typologies. Mangroves had limited regeneration 26 months after the storms, and recovery on St. John may be hindered by pre-storm hydrologic change in some stands, and potential genetic bottlenecks and lack of propagule sources for expedient recovery in all stands.

St Johns↗

USGS2024

Modeling the responses of blue carbon fluxes in Mississippi River Deltaic Plain brackish marshes to climate change induced hydrologic conditions

Carbon fluxes in tidal brackish marshes play a critical role in determining coastal wetland carbon sequestration and storage, thus affecting carbon crediting of coastal wetland restoration. In this study, a process-driven wetland biogeochemistry model, Wetland Carbon Assessment Tool DeNitrification-DeComposition was applied to nine brackish marsh sites in Mississippi River (MR) Deltaic Plain to examine the responses of gross primary productivity (GPP), ecosystem respiration (ER), net ecosystem exchange (NEE), and emissions of methane (CH 4 ) and nitrous oxide (N 2 O) to climate change. Simulations of a normal hydrologic year (2013), dry year (2011) and wet year (2021), and a hypothetical sea level rise (SLR) case were conducted as climate change scenarios. These climate change scenarios were determined by the Palmer Drought Severity Index (PDSI) for the Northeast Division of Coastal Louisiana during 2001–2021. Model results showed that GPP, ER, NEE, CH 4 , and N 2 O vary with site, and these brackish marshes lost carbon (net CO 2 emission) due to large reduction in primary productivity under the climate scenarios, as well as even during the normal hydrologic year. Average cross-site NEE were 148, 140 and 132 g C m −2 yr −1 in the dry, wet, and normal years (all net loss of wetland C). Under the hypothetical SLR, NEE were reduced by -25% compared to the normal year, but GPP and NPP were declined by -40% and -70%, respectively. These results suggest that climate change induced changes in soil salinity and water table depth will exacerbate carbon loss from tidal brackish marshes.

Louisiana↗

USGS1992

Comparison of methods for the removal of organic carbon and extraction of chromium, iron and manganese from an estuarine sediment standard and sediment from the Calcasieu River estuary, Louisiana, U.S.A.

U.S. National Bureau of Standards (NBS) estuarine sediment 1646 from the Chesapeake Bay, Maryland, and surface sediment collected at two sites in the Calcasieu River estuary, Louisiana, were used to evaluate the dilute hydrochloric acid extraction of Cr, Fe and Mn from air-dried and freeze-dried samples that had been treated by one of three methods to remove organic carbon. The three methods for the oxidation and removal of organic carbon were: (1) 30% hydrogen peroxide; (2) 30% hydrogen peroxide plus 0.25 mM pyrophosphate; and (3) plasma oxidation (low-temperature ashing). There was no statistically significant difference at the 95% confidence level between air- and freeze-dried samples with respect to the percent of organic carbon removed by the three methods. Generally, there was no statistically significant difference at the 95% confidence level between air- and freeze-dried samples with respect to the concentration of Cr, Fe and Mn that was extracted, regardless of the extraction technique that was used. Hydrogen peroxide plus pyrophosphate removed the most organic carbon from sediment collected at the site in the Calcasieu River that was upstream from industrial outfalls. Plasma oxidation removed the most organic carbon from the sediment collected at a site in the Calcasieu River close to industrial outfalls and from the NBS estuarine sediment sample. Plasma oxidation merits further study as a treatment for removal of organic carbon. Operational parameters can be chosen to limit the plasma oxidation of pyrite which, unlike other Fe species, will not be dissolved by dilute hydrochloric acid. Preservation of pyrite allows the positive identification of Fe present as pyrite in sediments.

Chemical Geology↗

USGS1971

Calcium-magnesium carbonate solid solutions from Holocene conglomerate cements and travertines in the Coast Range of California

Two calcium-magnesium carbonate solid solutions form Holocene travertines and conglomerate cements in fresh water stream channels of the Coast Range of California. Calcite does not yield the {015} diffraction maximum. The {006} diffraction maximum is lacking over most of the range of composition of calcite. Calcite has compositions from CaCO 3 to Ca 0.5 Mg 0.5 CO 3 . Dolomite yields both the {006} and {015} diffraction maxima over its entire composition range, Ca 0.6 Mg 0.4 CO 3 to Ca 0.5 Mg 0.5 CO 3 . The Ca-Mg carbonates form in isotopic equilibrium and thermodynamic disequilibrium from dispersion of Ca 2+ -rich water into CO 3 2− -rich water within the alluvium. The stable isotope data suggest that all the Mg-rich carbonates are primary precipitates and not a result of Mg-substitution in precursor CaCO 3 . There is a correlation between δC 13 and Mg content of the carbonates which predicts a 5%. fractionation of C 13 between dolomite and calcite at sedimentary temperatures. C 14 is incorporated in Ca-Mg carbonates forming from C 13 -poor meteoric waters and C 13 -rich waters from Cretaceous sediments. C 14 ages of the Ca-Mg carbonates are apparent, and cannot be corrected to absolute values. Solution rates of calcite decrease with increasing MgCO 3 content; dolomite dissolves slower than any calcite.

California↗

USGS1989

Carbon isotope effects associated with autotrophic acetogenesis

The carbon kinetic isotope effects associated with synthesis of acetate from CO 2 and H 2 during autotrophic growth of Acetobacterium woodii at 30°C have been measured by isotopic analyses of CO 2 , methyl-carbon, and total acetate. Closed systems allowing construction of complete mass balances at varying stages of growth were utilized, and the effects of the partitioning of carbon between CO 2 and HCO 3 − were taken into account. For the overall reaction, total carbonate → total acetate, isotope effects measured in replicate experiments ranged from −59.0 ± 0.9% to − 57.2 ± 2.3 z %. Taking into account all measurements, the weighted mean and standard deviation are −58.6 ± 0.7%. There is no evidence for intramolecular ordering in the acetate. The carbon isotopic composition of sedimentary acetate, otherwise expected to be near that of sedimentary organic carbon, is likely to be depleted in environments in which autotrophic acetogenesis is occurring.

Organic Geochemistry↗

USGS1985

Dissolution of barite for the analysis of strontium isotopes and other chemical and isotopic variations using aqueous sodium carbonate

A simple procedure for preparing barite samples for chemical and isotopic analysis is described. Sulfate ion, in barite, in the presence of high concentrations of aqueous sodium carbonate, is replaced by carbonate. This replacement forms insoluble carbonates with the cations commonly in barite: Ba, Sr, Ca and Pb. Sulfate is released into the solution by the carbonate replacement and is separated by filtration. The aqueous sulfate can then be reprecipitated for analysis of the sulfur and oxygen isotopes. The cations in the carbonate phase can be dissolved by acidifying the solid residue. Sr can be separated from the solution for Sr isotope analysis by ion-exchange chromatography. The sodium carbonate used contains amounts of Sr which will affect almost all barite 87 Sr 86 Sr "> 87Sr86Sr ratios by less than 0.00001 at 1.95θ of the mean. The procedure is preferred over other techniques used for preparing barite samples for the determination of 87 Sr 86 Sr "> 87Sr86Sr ratios because it is simple, rapid and enables simultaneous determination of many compositional parameters on the same material.

Chemical Geology: Isotope Geoscience Section↗

USGS1983

The nature of carbon dioxide waters in Snaefellsnes, western Iceland

Over 20 occurrences of thermal and non-thermal waters rich in carbon dioxide are known in the Snaefellsnes Peninsula of western Iceland. On the basis of the thermal, chemical and isotopic characteristics of these waters, and hydrological considerations, it is concluded that they represent meteoric waters which have seeped to variable depths into the bedrock. Ascending carbon dioxide gas originating from intrusions or the mantle mixes with the meteoric waters to produce carbon dioxide waters: at considerable depth in the case of the thermal carbon dioxide waters but close to the surface in the case of cold carbon dioxide waters. The occurrence of carbon dioxide waters cannot be regarded as evidence for underground geothermal reservoirs.

Geothermics↗

USGS2012

Carbonate aquifers

Only limited hydrogeological research has been conducted using ichnology in carbonate aquifer characterization. Regardless, important applications of ichnology to carbonate aquifer characterization include its use to distinguish and delineate depositional cycles, correlate mappable biogenically altered surfaces, identify zones of preferential groundwater flow and paleogroundwater flow, and better understand the origin of ichnofabric-related karst features. Three case studies, which include Pleistocene carbonate rocks of the Biscayne aquifer in southern Florida and Cretaceous carbonate strata of the Edwards–Trinity aquifer system in central Texas, demonstrate that (1) there can be a strong relation between ichnofabrics and groundwater flow in carbonate aquifers and (2) ichnology can offer a useful methodology for carbonate aquifer characterization. In these examples, zones of extremely permeable, ichnofabric-related macroporosity are mappable stratiform geobodies and as such can be represented in groundwater flow and transport simulations.

Florida;Texas↗