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USGS2021

Carbon fluxes and potential soil accumulation within Greater Everglades cypress and pine forested wetlands

In forested wetlands, accumulation of organic matter in soil is partly governed by carbon fluxes where photosynthesis, respiration, lateral advection of waterborne carbon, fire-derived carbon emissions, and methanogenesis are balanced by changes in stored carbon. Stored carbon can eventually accumulate as soil over time if net primary productivity exceeds biomass decomposition. For this study, potential soil accumulation was estimated based on four years of continuous daily carbon cycling data and a one-dimensional mass-balance model of landscape-atmospheric exchange for cypress and pine forested wetlands in the Greater Everglades of south Florida. The mass-balance model was driven by eddy-covariance estimates of vertical net ecosystem exchange of carbon dioxide and methane. Key findings include confirmation of a basic premise of the historic Everglades restoration project; specifically, more water either from rainfall or water management encourages soil carbon accumulation and thus conservation of soils that support biologic activity and ecosystem services. For example, an anomalous wet season for south Florida that flooded the forested wetlands through the traditional dry season was followed by the most productive year for photosynthetic carbon uptake and potential soil accumulation. On the other hand, methane emissions were enhanced by the anomalous wet season and extended flooding – which confirmed a complex tradeoff to consider if wetlands are managed for both soil conservation and reduction of greenhouse gas emissions. Potential soil accumulation rates were about 1.7, 2.8, and 18 millimeters per year at the Dwarf Cypress, Cypress Swamp, and Pine Upland ecosystems, assuming soil C density values of 0.07, 0.09, and 0.02 grams of carbon per cubic centimeter, respectively. For these values of soil C density, the accumulation rates are considered a “best-case” upper limit because the lateral export of carbon in the canals and creeks that drain the study area were assumed negligible.

Florida↗

USGS2017

Carbon dynamics of river corridors and the effects of human alterations

Research in stream metabolism, gas exchange, and sediment dynamics indicates that rivers are an active component of the global carbon cycle and that river form and process can influence partitioning of terrestrially derived carbon among the atmosphere, geosphere, and ocean. Here we develop a conceptual model of carbon dynamics (inputs, outputs, and storage of organic carbon) within a river corridor, which includes the active channel and the riparian zone. The exchange of carbon from the channel to the riparian zone represents potential for storage of transported carbon not included in the “active pipe” model of organic carbon (OC) dynamics in freshwater systems. The active pipe model recognizes that river processes influence carbon dynamics, but focuses on CO 2 emissions from the channel and eventual delivery to the ocean. We also review how human activities directly and indirectly alter carbon dynamics within river corridors. We propose that dams create the most significant alteration of carbon dynamics within a channel, but that alteration of riparian zones, including the reduction of lateral connectivity between the channel and riparian zone, constitutes the most substantial change of carbon dynamics in river corridors. We argue that the morphology and processes of a river corridor regulate the ability to store, transform, and transport OC, and that people are pervasive modifiers of river morphology and processes. The net effect of most human activities, with the notable exception of reservoir construction, appears to be that of reducing the ability of river corridors to store OC within biota and sediment, which effectively converts river corridors to OC sources rather than OC sinks. We conclude by summarizing knowledge gaps in OC dynamics and the implications of our findings for managing OC dynamics within river corridors.

Ecological Monographs↗

USGS2013

An evaluation of temporal changes in sediment accumulation and impacts on carbon burial in Mobile Bay, Alabama, USA

The estuarine environment can serve as either a source or sink of carbon relative to the coastal ocean carbon budget. A variety of time-dependent processes such as sedimentation, carbon supply, and productivity dictate how estuarine systems operate, and Mobile Bay is a system that has experienced both natural and anthropogenic perturbations that influenced depositional processes and carbon cycling. Sediments from eight box cores provide a record of change in bulk sediment accumulation and carbon burial over the past 110 years. Accumulation rates in the central part of the basin (0.09 g cm −2 ) were 60–80 % less than those observed at the head (0.361 g cm −2 ) and mouth (0.564 g cm −2 ) of the bay. Sediment accumulation in the central bay decreased during the past 90 years in response to both anthropogenic (causeway construction) and natural (tropical cyclones) perturbations. Sediment accumulation inevitably increased the residence time of organic carbon in the oxic zone, as observed in modeled remineralization rates, and reduced the overall carbon burial. Such observations highlight the critical balance among sediment accumulation, carbon remineralization, and carbon burial in dynamic coastal environments. Time-series analysis based solely on short-term observation would not capture the long-term effects of changes in sedimentation on carbon cycling. Identifying these relationships over longer timescales (multi-annual to decadal) will provide a far better evaluation of coastal ocean carbon budgets.

Alabama↗

USGS2007

Authigenic carbonate formation at hydrocarbon seeps in continental margin sediments: A comparative study

Authigenic carbonates from five continental margin locations, the Eel River Basin, Monterey Bay, Santa Barbara Basin, the Sea of Okhotsk, and the North Sea, exhibit a wide range of mineralogical and stable isotopic compositions. These precipitates include aragonite, low- and high-Mg calcite, and dolomite. The carbon isotopic composition of carbonates varies widely, ranging from −60‰ to +26‰, indicating complex carbon sources that include 13 C-depleted microbial and thermogenic methane and residual, 13 C-enriched, bicarbonate. A similarly large variability of δ 18 O values (−5.5‰ to +8.9‰) demonstrates the geochemical complexity of these sites, with some samples pointing toward an 18 O-enriched oxygen source possibly related to advection of 18 O-enriched formation water or to the decomposition of gas hydrate. Samples depleted in 18 O are consistent with formation deeper in the sediment or mixing of pore fluids with meteoric water during carbonate precipitation. A wide range of isotopic and mineralogical variation in authigenic carbonate composition within individual study areas but common trends across multiple geographic areas suggest that these parameters alone are not indicative for certain tectonic or geochemical settings. Rather, the observed variations probably reflect local controls on the flux of carbon and other reduced ions, such as faults, fluid conduits, the presence or absence of gas hydrate in the sediment, and the temporal evolution of the local carbon reservoir. Areas with seafloor carbonates that indicate formation at greater depth below the sediment–water interface must have undergone uplift and erosion in the past or are still being uplifted. Consequently, the occurrence of carbonate slabs on the seafloor in areas of active hydrocarbon seepage is commonly an indicator of exhumation following carbonate precipitation in the shallow subsurface. Therefore, careful petrographic and geochemical analyses are critical components necessary for the correct interpretation of processes related to hydrocarbon seepage in continental margin environments and elsewhere.

Deep-Sea Research Part II: Topical Studies in Ocea↗

USGS2016

Evaluating land cover influences on model uncertainties—A case study of cropland carbon dynamics in the Mid-Continent Intensive Campaign region

Quantifying spatial and temporal patterns of carbon sources and sinks and their uncertainties across agriculture-dominated areas remains challenging for understanding regional carbon cycles. Characteristics of local land cover inputs could impact the regional carbon estimates but the effect has not been fully evaluated in the past. Within the North American Carbon Program Mid-Continent Intensive (MCI) Campaign, three models were developed to estimate carbon fluxes on croplands: an inventory-based model, the Environmental Policy Integrated Climate (EPIC) model, and the General Ensemble biogeochemical Modeling System (GEMS) model. They all provided estimates of three major carbon fluxes on cropland: net primary production (NPP), net ecosystem production (NEP), and soil organic carbon (SOC) change. Using data mining and spatial statistics, we studied the spatial distribution of the carbon fluxes uncertainties and the relationships between the uncertainties and the land cover characteristics. Results indicated that uncertainties for all three carbon fluxes were not randomly distributed, but instead formed multiple clusters within the MCI region. We investigated the impacts of three land cover characteristics on the fluxes uncertainties: cropland percentage, cropland richness and cropland diversity. The results indicated that cropland percentage significantly influenced the uncertainties of NPP and NEP, but not on the uncertainties of SOC change. Greater uncertainties of NPP and NEP were found in counties with small cropland percentage than the counties with large cropland percentage. Cropland species richness and diversity also showed negative correlations with the model uncertainties. Our study demonstrated that the land cover characteristics contributed to the uncertainties of regional carbon fluxes estimates. The approaches we used in this study can be applied to other ecosystem models to identify the areas with high uncertainties and where models can be improved to reduce overall uncertainties for regional carbon flux estimates.

Mid-Continent Intensive Campaign region↗

USGS2016

Insights into methane dynamics from analysis of authigenic carbonates and chemosynthetic mussels at newly-discovered Atlantic Margin seeps

The recent discovery of active methane venting along the US northern and mid-Atlantic margin represents a new source of global methane not previously accounted for in carbon budgets from this region. However, uncertainty remains as to the origin and history of methane seepage along this tectonically inactive passive margin. Here we present the first isotopic analyses of authigenic carbonates and methanotrophic deep-sea mussels, Bathymodiolus sp., and the first direct constraints on the timing of past methane emission, based on samples collected at the upper slope Baltimore Canyon (&sim;385 m water depth) and deepwater Norfolk (&sim;1600 m) seep fields within the area of newly-discovered venting. The authigenic carbonates at both sites were dominated by aragonite, with an average signature of −47&permil; , a value consistent with microbially driven anaerobic oxidation of methane-rich fluids occurring at or near the sediment–water interface. Authigenic carbonate U and Sr isotope data further support the inference of carbonate precipitation from seawater-derived fluids rather than from formation fluids from deep aquifers. Carbonate stable and radiocarbon ( and ) isotope values from living Bathymodiolus sp. specimens are lighter than those of seawater dissolved inorganic carbon, highlighting the influence of fossil carbon from methane on carbonate precipitation. U–Th dates on authigenic carbonates suggest seepage at Baltimore Canyon between 14.7±0.6 ka to 15.7±1.6 ka , and at the Norfolk seep field between 1.0±0.7 ka to 3.3±1.3 ka , providing constraint on the longevity of methane efflux at these sites. The age of the brecciated authigenic carbonates and the occurrence of pockmarks at the Baltimore Canyon upper slope could suggest a link between sediment delivery during Pleistocene sea-level lowstand, accumulation of pore fluid overpressure from sediment compaction, and release of overpressure through subsequent venting. Calculations show that the Baltimore Canyon site probably has not been within the gas hydrate stability zone (GHSZ) in the past 20 ka, meaning that in-situ release of methane from dissociating gas hydrate cannot be sustaining the seep. We cannot rule out updip migration of methane from dissociation of gas hydrate that occurs farther down the slope as a source of the venting at Baltimore Canyon, but consider that the history of rapid sediment accumulation and overpressure may play a more important role in methane emissions at this site.

Baltimore Canyon seep fields, Norfolk seep fields↗

USGS2007

Soils at the hyperarid margin: The isotopic composition of soil carbonate from the Atacama Desert, Northern Chile

We evaluate the impact of exceptionally sparse plant cover (0–20%) and rainfall (2–114 mm/yr) on the stable carbon and oxygen composition of soil carbonate along elevation transects in what is among the driest places on the planet, the Atacama Desert in northern Chile. δ 13 C and δ 18 O values of carbonates from the Atacama are the highest of any desert in the world. δ 13 C (VPDB) values from soil carbonate range from -8.2% at the wettest sites to +7.9% at the driest. We measured plant composition and modeled respiration rates required to form these carbonate isotopic values using a modified version of the soil diffusion model of [Cerling (1984) Earth Planet. Sci. Lett. 71 , 229–240], in which we assumed an exponential form of the soil CO 2 production function, and relatively shallow (20–30 cm) average production depths. Overall, we find that respiration rates are the main predictor of the δ 13 C value of soil carbonate in the Atacama, whereas the fraction C 3 to C 4 biomass at individual sites has a subordinate influence. The high average δ 13 C value (+4.1%) of carbonate from the driest study sites indicates it formed-perhaps abiotically—in the presence of pure atmospheric CO 2 . δ 18 O (VPDB) values from soil carbonate range from -5.9% at the wettest sites to +7.3% at the driest and show much less regular variation with elevation change than δ 13 C values. δ 18 O values for soil carbonate predicted from local temperature and δ 18 O values of rainfall values suggest that extreme (>80% in some cases) soil dewatering by evaporation occurs at most sites prior to carbonate formation. The effects of evaporation compromise the use of δ 18 O values from ancient soil carbonate to reconstruct paleoelevation in such arid settings.

Atacama Desert↗

USGS2020

The mineral diversity of Jezero crater: Evidence for possible lacustrine carbonates on Mars

Noachian-aged Jezero crater is the only known location on Mars where clear orbital detections of carbonates are found in close proximity to clear fluvio-lacustrine features indicating the past presence of a paleolake; however, it is unclear whether or not the carbonates in Jezero are related to the lacustrine activity. This distinction is critical for evaluating the astrobiological potential of the site, as lacustrine carbonates on Earth are capable of preserving biosignatures at scales that may be detectable by a landed mission like the Mars 2020 rover, which is planned to land in Jezero in February 2021. In this study, we conduct a detailed investigation of the mineralogical and morphological properties of geological units within Jezero crater in order to better constrain the origin of carbonates in the basin and their timing relative to fluvio-lacustrine activity. Using orbital visible/near-infrared hyperspectral images from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) along with high resolution imagery and digital elevation models, we identify a distinct carbonate-bearing unit, the “Marginal Carbonates,” located along the inner margin of the crater, near the largest inlet valley and the western delta. Based on their strong carbonate signatures, topographic properties, and location in the crater, we propose that this unit may preserve authigenic lacustrine carbonates, precipitated in the near-shore environment of the Jezero paleolake. Comparison to carbonate deposits from terrestrial closed basin lakes suggests that if the Marginal Carbonates are lacustrine in origin, they could preserve macro- and microscopic biosignatures in microbialite rocks like stromatolites, some of which would likely be detectable by Mars 2020. The Marginal Carbonates may represent just one phase of a complex fluvio-lacustrine history in Jezero crater, as we find that the spectral diversity of the fluvio-lacustrine deposits in the crater is consistent with a long-lived lake system cataloging the deposition and erosion of regional geologic units. Thus, Jezero crater may contain a unique record of the evolution of surface environments, climates, and habitability on early Mars.

Icarus↗

USGS1997

Adsorbed natural gas storage with activated carbons made from Illinois coals and scrap tires

Activated carbons for natural gas storage were produced from Illinois bituminous coals (IBC-102 and IBC-106) and scrap tires by physical activation with steam or CO 2 and by chemical activation with KOH, H 3 PO 4 , or ZnCl 2 . The products were characterized for N 2 -BET area, micropore volume, bulk density, pore size distribution, and volumetric methane storage capacity ( V m / V s ). V m / V s values for Illinois coal-derived carbons ranged from 54 to 83 cm 3 /cm 3 , which are 35−55% of a target value of 150 cm 3 /cm 3 . Both granular and pelletized carbons made with preoxidized Illinois coal gave higher micropore volumes and larger V m / V s values than those made without preoxidation. This confirmed that preoxidation is a desirable step in the production of carbons from caking materials. Pelletization of preoxidized IBC-106 coal, followed by steam activation, resulted in the highest V m / V s value. With roughly the same micropore volume, pelletization alone increased V m / V s of coal carbon by 10%. Tire-derived carbons had V m / V s values ranging from 44 to 53 cm 3 /cm 3 , lower than those of coal carbons due to their lower bulk densities. Pelletization of the tire carbons increased bulk density up to 160%. However, this increase was offset by a decrease in micropore volume of the pelletized materials, presumably due to the pellet binder. As a result, V m / V s values were about the same for granular and pelletized tire carbons. Compared with coal carbons, tire carbons had a higher percentage of mesopores and macropores.

Energy and Fuels↗

USGS2003

Modeling carbon dynamics in vegetation and soil under the impact of soil erosion and deposition

Soil erosion and deposition may play important roles in balancing the global atmospheric carbon budget through their impacts on the net exchange of carbon between terrestrial ecosystem and the atmosphere. Few models and studies have been designed to assess these impacts. In this study, we developed a general ecosystem model, Erosion-Deposition-Carbon-Model (EDCM), to dynamically simulate the influences of rainfall-induced soil erosion and deposition on soil organic carbon (SOC) dynamics in soil profiles. EDCM was applied to several landscape positions in the Nelson Farm watershed in Mississippi, including ridge top (without erosion or deposition), eroding hillslopes, and depositional sites that had been converted from native forests to croplands in 1870. Erosion reduced the SOC storage at the eroding sites and deposition increased the SOC storage at the depositional areas compared with the site without erosion or deposition. Results indicated that soils were consistently carbon sources to the atmosphere at all landscape positions from 1870 to 1950, with lowest source strength at the eroding sites (13 to 24 gC m-2 yr-1), intermediate at the ridge top (34 gC m-2 yr-1), and highest at the depositional sites (42 to 49 gC m-2 yr-1). During this period, erosion reduced carbon emissions via dynamically replacing surface soil with subsurface soil that had lower SOC contents (quantity change) and higher passive SOC fractions (quality change). Soils at all landscape positions became carbon sinks from 1950 to 1997 due to changes in management practices (e.g., intensification of fertilization and crop genetic improvement). The sink strengths were highest at the eroding sites (42 to 44 gC m-2 yr-1 , intermediate at the ridge top (35 gC m-2 yr-1), and lowest at the depositional sites (26 to 29 gC m-2 yr-1). During this period, erosion enhanced carbon uptake at the eroding sites by continuously taking away a fraction of SOC that can be replenished with enhanced plant residue input. Overall, soil erosion and deposition reduced CO2 emissions from the soil into the atmosphere by exposing low carbon-bearing soil at eroding sites and by burying SOC at depositional sites. The results suggest that failing to account for the impact of soil erosion and deposition may potentially contribute to an overestimation of both the total historical carbon released from soils owing to land use change and the contemporary carbon sequestration rates at the eroding sites.

Global Biogeochemical Cycles↗

USGS2012

Hydrous carbonates on Mars?: Evidence from Mariner 6/7 infrared spectrometer and ground‐based telescopic spectra

Absorption features at 2.28 and 5.4 μm identified in Mariner 6/7 infrared spectrometer and terrestrial telescopic spectra are consistent with the spectra of hydrous magnesium carbonates such as hydromagnesite and artinite. Spectral characteristics of these hydrous carbonates are different from those of the anhydrous carbonates, as the former do not have the strong spectral features typically associated with anhydrous carbonates such as calcite and siderite. Theoretical mixing indicates that, depending on the type of hydrous carbonate, 10–20 wt % can be incorporated into the regolith without contradicting the spectral observations or the Viking x ray fluorescence chemical analysis. Hydrous carbonates form as weathering products of mafic minerals in the presence of H 2 O and CO 2 , even in the Antarctic. Their formation as evaporite minerals from either original magmas or hydrothermally altered rocks is consistent with the Martian environment, provided liquid water is or has been at least transiently present. On Earth, formation of hydrous Mg carbonates is associated with the production of amorphous iron oxides, which is consistent with both the environment and the inferred surface mineralogy of Mars. These minerals are about 60 wt % H 2 O, CO 3 , and OH; if they are abundant everywhere at the 10% level, then about 6% of the surface weight could be volatiles bound in this type of mineral. Although the stability of hydrous carbonates in a Martian environment is uncertain, there may be kinetic factors inhibiting the dehydration of these minerals, which may persist metastably in the current environment. Although the spectroscopic evidence for anhydrous carbonates is scant, the possible presence of hydrous carbonates provides an appealing mechanism for the existence of carbonates on Mars.

Journal of Geophysical Research↗

USGS2001

Carbon dynamics within agricultural and native sites in the loess region of Western lowa

In order to quantify the historical changes in carbon storage that result from agricultural conversion, this study compared the carbon dynamics of two sites in the loess region of Iowa: a native prairie and a cropland. Field data were obtained to determine present-day carbon storage and its variability within a landscape (a stable ridgetop vs. eroding upper-midslope vs. depositional lower slope). Models were used to recreate the historical carbon budget of these sites and determine the cropland's potential to be a net CO2 source or sink, relative to the atmosphere. Regardless of slope position, the cropland site contains approximately half the amount of carbon as prairie. Variability in soil carbon storage within a site as a consequence of slope position is as large or larger (variations of 200-300%) than temporal variation (???200% at all slope positions). The most extreme difference in soil carbon storage between the cropland and prairie sites is found in the soil at the upper-midslope, which is the area of greatest erosion. The models estimate that 93-172% of the carbon in the original topsoil has been lost from the cropland's eroding midslope. Much of this carbon is derived from deeper soil horizons. Either a small sink or strong source of carbon to the atmosphere is created, depending on the fate of the eroded sediment and its associated carbon.

Global Change Biology↗

USGS2001

Large carbon isotope fractionation associated with oxidation of methyl halides by methylotrophic bacteria

The largest biological fractionations of stable carbon isotopes observed in nature occur during production of methane by methanogenic archaea. These fractionations result in substantial (as much as ≈70‰) shifts in δ 13 C relative to the initial substrate. We now report that a stable carbon isotopic fractionation of comparable magnitude (up to 70‰) occurs during oxidation of methyl halides by methylotrophic bacteria. We have demonstrated biological fractionation with whole cells of three methylotrophs (strain IMB-1, strain CC495, and strain MB2) and, to a lesser extent, with the purified cobalamin-dependent methyltransferase enzyme obtained from strain CC495. Thus, the genetic similarities recently reported between methylotrophs, and methanogens with respect to their pathways for C 1 -unit metabolism are also reflected in the carbon isotopic fractionations achieved by these organisms. We found that only part of the observed fractionation of carbon isotopes could be accounted for by the activity of the corrinoid methyltransferase enzyme, suggesting fractionation by enzymes further along the degradation pathway. These observations are of potential biogeochemical significance in the application of stable carbon isotope ratios to constrain the tropospheric budgets for the ozone-depleting halocarbons, methyl bromide and methyl chloride. Methyl bromide (MeBr) and methyl chloride (MeCl) are, respectively, the most abundant volatile bromo- and chlorocarbons in the troposphere and are major contributors to stratospheric ozone destruction (1). Both compounds have natural and human-influenced sources and a predominant sink by reaction with OH in the troposphere (2–4). MeBr also has a bacterial soil sink (5) that represents about 20% of the estimated total removal from the troposphere, and it is likely that a soil sink of similar magnitude exists for MeCl (6). Hence, if an isotopic fractionation is associated with the soil sink, it will influence the isotopic compositions of MeBr and MeCl in the lower atmosphere (7). The δ 13 C value of industrially produced MeBr ranges between −43.5‰ and −66.4‰ (7), but δ 13 C values of tropospheric MeBr and natural sources are not yet known. The δ 13 C of atmospheric MeCl has been measured from −22‰ to −45‰ (8, 9). If carbon isotope ratios are to be used to constrain the budgets of these methyl halides, it is essential to determine the extent of carbon isotope fractionation that occurs during biological degradation of these compounds. Methylotrophic bacteria use C 1 compounds, which are simple organic molecules that contain no carbon–carbon bonds. Strains IMB-1, CC495, and MB2 are as-yet-unnamed facultative methylotrophs isolated from agricultural soil, woodland leaf litter, and coastal seawater, respectively (10–13), environments where methyl halides are produced. They are members of the α subgroup of the Proteobacteria . On the basis of 16S rRNA gene sequences, strains IMB-1 and CC495 show some phylogenetic alignment with the genus Rhizobium (10, 11) and are very closely related to the new genus Pseudoaminobacte r (I. McDonald, personal communication). Strain MB2 aligns within the Ruegeria clade [J. K. Schaefer, K. D. Goodwin, I. R. McDonald, J. C. Murrell and R.S.O., unpublished work]. All of these aerobic bacteria are methylotrophs in that they can grow by using MeBr or MeCl as their sole carbon source, but they do not metabolize methane. They oxidize MeBr, MeCl, and methyl iodide (MeI) to CO 2 . Soil bacteria are known to consume MeBr at the ambient tropospheric mixing ratio of around 10 parts per trillion by volume (5). Preliminary experiments with strain IMB-1 indicate that it can oxidize MeBr at these mixing ratios** and is therefore likely to be characteristic of bacteria associated with MeBr uptake by soils. We examined δ 13 C of MeCl, MeBr, and MeI during oxidation by whole-cell suspensions of IMB-1 and CC495 and also the change in δ 13 C values of the three methyl halides during oxidation by the marine strain MB2. In addition, we measured the fractionation of carbon isotopes during formation of methane thiol (MeSH) from MeCl by the purified cobalamin-dependent enzyme, halomethane:bisulphide/halide ion methyltransferase (11) from CC495, to determine whether this initial step in MeCl degradation could account for the observed fractionation by whole cells. Finally, we determined the fractionation associated with the degradation of MeBr during field studies with agricultural soil by monitoring MeBr concentration and δ 13 C of MeBr in the headspace of flux chambers under fumigation conditions.

Proceedings of the National Academy of Sciences of↗

USGS2021

Ecosystem carbon balance in the Hawaiian Islands under different scenarios of future climate and land use change

The State of Hawai'i passed legislation to be carbon neutral by 2045, a goal that will partly depend on carbon sequestration by terrestrial ecosystems. However, there is considerable uncertainty surrounding the future direction and magnitude of the land carbon sink in the Hawaiian Islands. We used the Land Use and Carbon Scenario Simulator (LUCAS), a spatially explicit stochastic simulation model that integrates landscape change and carbon gain-loss, to assess how projected future changes in climate and land use will influence ecosystem carbon balance in the Hawaiian Islands under all combinations of two radiative forcing scenarios (RCPs 4.5 and 8.5) and two land use scenarios (low and high) over a 90 year timespan from 2010 to 2100. Collectively, terrestrial ecosystems of the Hawaiian Islands acted as a net carbon sink under low radiative forcing (RCP 4.5) for the entire 90 year simulation period, with low land use change further enhancing carbon sink strength. In contrast, Hawaiian terrestrial ecosystems transitioned from a net sink to a net source of CO 2 to the atmosphere under high radiative forcing (RCP 8.5), with high land use accelerating this transition and exacerbating net carbon loss. A sensitivity test of the CO 2 fertilization effect on plant productivity revealed it to be a major source of uncertainty in projections of ecosystem carbon balance, highlighting the need for greater mechanistic understanding of plant productivity responses to rising atmospheric CO 2 . Long-term model projections such as ours that incorporate the interactive effects of land use and climate change on regional ecosystem carbon balance will be critical to evaluating the potential of ecosystem-based climate mitigation strategies.

Hawaii↗

USGS2020

From pools to flow: The PROMISE framework for new insights on soil carbon cycling in a changing world

Soils represent the largest terrestrial reservoir of organic carbon, and the balance between soil organic carbon (SOC) formation and loss will drive powerful carbon‐climate feedbacks over the coming century. To date, efforts to predict SOC dynamics have rested on pool‐based models, which assume classes of SOC with internally homogenous physicochemical properties. However, emerging evidence suggests that soil carbon turnover is not dominantly controlled by the chemistry of carbon inputs, but rather by restrictions on microbial access to organic matter in the spatially heterogeneous soil environment. The dynamic processes that control the physicochemical protection of carbon translate poorly to pool‐based SOC models; as a result, we are challenged to mechanistically predict how environmental change will impact movement of carbon between soils and the atmosphere. Here, we propose a novel conceptual framework to explore controls on belowground carbon cycling: P robabilistic R epresentation of O rganic M atter I nteractions within the S oil E nvironment (PROMISE). In contrast to traditional model frameworks, PROMISE does not attempt to define carbon pools united by common thermodynamic or functional attributes. Rather, the PROMISE concept considers how SOC cycling rates are governed by the stochastic processes that influence the proximity between microbial decomposers and organic matter, with emphasis on their physical location in the soil matrix. We illustrate the applications of this framework with a new biogeochemical simulation model that traces the fate of individual carbon atoms as they interact with their environment, undergoing biochemical transformations and moving through the soil pore space. We also discuss how the PROMISE framework reshapes dialogue around issues related to SOC management in a changing world. We intend the PROMISE framework to spur the development of new hypotheses, analytical tools, and model structures across disciplines that will illuminate mechanistic controls on the flow of carbon between plant, soil, and atmospheric pools.

Global Change Biology↗

USGS2000

Sources and yields of dissolved carbon in northern Wisconsin stream catchments with differing amounts of Peatland

In five tributary streams (four inflowing and one outflowing) of 1600-ha Trout Lake in northern Wisconsin, USA, we examined factors that can affect the magnitude of stream flow and transport of dissolved organic and inorganic carbon (DOC and DIC) through the streams to the lake. One catchment, the Allequash Creek basin, was investigated in more detail to describe the dynamics of carbon flow and to identify potential carbon sources. Stream flows and carbon loads showed little or no relation to surface-water catchment area. They were more closely related to ground-water watershed area because ground-water discharge, from both local and regional sources, is a major contributor to the hydrologic budgets of these catchments. An important factor in determining carbon influx to the stream is the area of peatland in the catchment. Peatland porewaters contain DOC concentrations up to 40 mg 1 −1 and are a significant potential carbon source. Ground-water discharge and lateral flow through peat are the suspected mechanisms for transport of that carbon to the streams. Carbon and nitrogen isotopes suggested that the sources of DOC in Allequash Creek above Allequash Lake were wetland vegetation and peat and that the sources below Allequash Lake were filamentous algae and wild rice. Catchments with high proportions of peatland, including the Allequash Creek catchment, tended to have elevated DOC loads in outflowing stream water. Respiration and carbon mineralization in lakes within the system tend to produce low DOC and low DOC/DIC in lake outflows, especially at Trout Lake. In Allequash Lake, however, the shallow peat island and vegetation-filled west end were sources of DOC. Despite the vast carbon reservoir in the peatlands, carbon yields were very low in these catchments. Maximum yields were on the order of 2.5 g m −2 y −1 DOC and 5.5 g m −2 y −1 DIC. The small yields were attributable to low stream flows due to lack of significant overland runoff and very limited stream channel coverage of the total catchment area.

Wisconsin↗

USGS2012

Concentrations, loads, and yields of organic carbon in streams of agricultural watersheds

Carbon is cycled to and from large reservoirs in the atmosphere, on land, and in the ocean. Movement of organic carbon from the terrestrial reservoir to the ocean plays an important role in the global cycling of carbon. The transition from natural to agricultural vegetation can change the storage and movement of organic carbon in and from a watershed. Samples were collected from 13 streams located in hydrologically and agriculturally diverse watersheds, to better understand the variability in the concentrations and loads of dissolved organic carbon (DOC) and particulate organic carbon (POC) in the streams, and the variability in watershed yields. The overall annual median concentrations of DOC and POC were 4.9 (range: 2.1–6.8) and 1.1 (range: 0.4–3.8) mg C L −1 , respectively. The mean DOC watershed yield (± SE) was 25 ± 6.8 kg C ha −1 yr −1 . The yields of DOC from these agricultural watersheds were not substantially different than the DOC yield from naturally vegetated watersheds in equivalent biomes, but were at the low end of the range for most biomes. Total organic carbon (DOC + POC) annually exported from the agricultural watersheds was found to average 0.03% of the organic carbon that is contained in the labile plant matter and top 1 m of soil in the watershed. Since the total organic carbon exported from agricultural watersheds is a relatively small portion of the sequestered carbon within the watershed, there is the great potential to store additional carbon in plants and soils of the watershed, offsetting some anthropogenic CO2 emissions.

California;Indiana;Iowa;Maryl;Mississippi;Nebraska↗

USGS2001

A guide to potential soil carbon sequestration: Land-use management for mitigation of greenhouse gas emissions

Terrestrial carbon sequestration has a potential role in reducing the recent increase in atmospheric carbon dioxide (CO2) that is, in part, contributing to global warming. Because the most stable long-term surface reservoir for carbon is the soil, changes in agriculture and forestry can potentially reduce atmospheric CO2 through increased soil-carbon storage. If local governments and regional planning agencies are to effect changes in land-use management that could mitigate the impacts of increased greenhouse gas (GHG) emissions, it is essential to know how carbon is cycled and distributed on the landscape. Only then can a cost/benefit analysis be applied to carbon sequestration as a potential land-use management tool for mitigation of GHG emissions. For the past several years, the U.S. Geological Survey (USGS) has been researching the role of terrestrial carbon in the global carbon cycle. Data from these investigations now allow the USGS to begin to (1) 'map' carbon at national, regional, and local scales; (2) calculate present carbon storage at land surface; and (3) identify those areas having the greatest potential to sequester carbon.

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