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At least 289 records · Page 16Linked to original sources

USGS2003

Effects of dissolved carbonate on arsenate adsorption and surface speciation at the hematite-water interface

Effects of dissolved carbonate on arsenate [As(V)] reactivity and surface speciation at the hematite−water interface were studied as a function of pH and two different partial pressures of carbon dioxide gas [ P CO 2 = 10 - 3.5 atm and ∼0; CO 2 -free argon (Ar)] using adsorption kinetics, pseudo-equilibrium adsorption/titration experiments, extended X-ray absorption fine structure spectroscopic (EXAFS) analyses, and surface complexation modeling. Different adsorbed carbonate concentrations, due to the two different atmospheric systems, resulted in an enhanced and/or suppressed extent of As(V) adsorption. As(V) adsorption kinetics [4 g L - 1 , [As(V)] 0 = 1.5 mM and I = 0.01 M NaCl] showed carbonate-enhanced As(V) uptake in the air-equilibrated systems at pH 4 and 6 and at pH 8 after 3 h of reaction. Suppressed As(V) adsorption was observed in the air-equilibrated system in the early stages of the reaction at pH 8. In the pseudo-equilibrium adsorption experiments [1 g L - 1 , [As(V)] 0 = 0.5 mM and I = 0.01 M NaCl], in which each pH value was held constant by a pH-stat apparatus, effects of dissolved carbonate on As(V) uptake were almost negligible at equilibrium, but titrant (0.1 M HCl) consumption was greater in the air-equilibrated systems ( P CO 2 = 10 - 3.5 atm) than in the CO 2 -free argon system at pH 4−7.75. The EXAFS analyses indicated that As(V) tetrahedral molecules were coordinated on iron octahedral via bidentate mononuclear (≈2.8 Å) and bidentate binuclear (≈3.3 Å) bonding at pH 4.5−8 and loading levels of 0.46−3.10 μM m - 2 . Using the results of the pseudo-equilibrium adsorption data and the XAS analyses, the pH-dependent As(V) adsorption under the P CO 2 = 10 - 3.5 atm and the CO 2 -free argon system was modeled using surface complexation modeling, and the results are consistent with the formation of nonprotonated bidentate surface species at the hematite surfaces. The results also suggest that the acid titrant consumption was strongly affected by changes to electrical double-layer potentials caused by the adsorption of carbonate in the air-equilibrated system. Overall results suggest that the effects of dissolved carbonate on As(V) adsorption were influenced by the reaction conditions [e.g., available surface sites, initial As(V) concentrations, and reaction times]. Quantifying the effects of adsorbed carbonate may be important in predicting As(V) transport processes in groundwater, where iron oxide-coated aquifer materials are exposed to seasonally fluctuating partial pressures of CO 2 (g).

Environmental Science & Technology↗

USGS1999

Dynamic replacement and loss of soil carbon on eroding cropland

Links between erosion/sedimentation history and soil carbon cycling were examined in a highly erosive setting in Mississippi loess soils. We sampled soils on (relatively) undisturbed and cropped hillslopes and measured C, N, 14 C, and CO 2 flux to characterize carbon storage and dynamics and to parameterize Century and spreadsheet 14 C models for different erosion and tillage histories. For this site, where 100 years of intensive cotton cropping were followed by fertilization and contour plowing, there was an initial and dramatic decline in soil carbon content from 1870 to 1950, followed by a dramatic increase in soil carbon. Soil erosion amplifies C loss and recovery: About 100% of the original, prehistoric soil carbon was likely lost over 127 years of intensive land use, but about 30% of that carbon was replaced after 1950. The eroded cropland was therefore a local sink for CO 2 since the 1950s. However, a net CO 2 sink requires a full accounting of eroded carbon, which in turn requires that decomposition rates in lower slopes or wetlands be reduced to about 20% of the upland value. As a result, erosion may induce unaccounted sinks or sources of CO 2 , depending on the fate of eroded carbon and its protection from decomposition. For erosion rates typical of the United States, the sink terms may be large enough (1 Gt yr −1 , back‐of‐the‐envelope) to warrant a careful accounting of site management, cropping, and fertilization histories, as well as burial rates, for a more meaningful global assessment.

Global Biogeochemical Cycles↗

USGS2001

Carbon balance of the terrestrial biosphere in the twentieth century: analyses of CO 2 , climate and land use effects with four process-based ecosystem models

The concurrent effects of increasing atmospheric CO 2 concentration, climate variability, and cropland establishment and abandonment on terrestrial carbon storage between 1920 and 1992 were assessed using a standard simulation protocol with four process-based terrestrial biosphere models. Over the long-term(1920–1992), the simulations yielded a time history of terrestrial uptake that is consistent (within the uncertainty) with a long-term analysis based on ice core and atmospheric CO 2 data. Up to 1958, three of four analyses indicated a net release of carbon from terrestrial ecosystems to the atmosphere caused by cropland establishment. After 1958, all analyses indicate a net uptake of carbon by terrestrial ecosystems, primarily because of the physiological effects of rapidly rising atmospheric CO 2 . During the 1980s the simulations indicate that terrestrial ecosystems stored between 0.3 and 1.5 Pg C yr−1, which is within the uncertainty of analysis based on CO 2 and O 2 budgets. Three of the four models indicated (in accordance with O 2 evidence) that the tropics were approximately neutral while a net sink existed in ecosystems north of the tropics. Although all of the models agree that the long-term effect of climate on carbon storage has been small relative to the effects of increasing atmospheric CO 2 and land use, the models disagree as to whether climate variability and change in the twentieth century has promoted carbon storage or release. Simulated interannual variability from 1958 generally reproduced the El Niño/Southern Oscillation (ENSO)-scale variability in the atmospheric CO 2 increase, but there were substantial differences in the magnitude of interannual variability simulated by the models. The analysis of the ability of the models to simulate the changing amplitude of the seasonal cycle of atmospheric CO 2 suggested that the observed trend may be a consequence of CO 2 effects, climate variability, land use changes, or a combination of these effects. The next steps for improving the process-based simulation of historical terrestrial carbon include (1) the transfer of insight gained from stand-level process studies to improve the sensitivity of simulated carbon storage responses to changes in CO 2 and climate, (2) improvements in the data sets used to drive the models so that they incorporate the timing, extent, and types of major disturbances, (3) the enhancement of the models so that they consider major crop types and management schemes, (4) development of data sets that identify the spatial extent of major crop types and management schemes through time, and (5) the consideration of the effects of anthropogenic nitrogen deposition. The evaluation of the performance of the models in the context of a more complete consideration of the factors influencing historical terrestrial carbon dynamics is important for reducing uncertainties in representing the role of terrestrial ecosystems in future projections of the Earth system.

Global Biogeochemical Cycles↗

USGS2004

Weathering controls on mechanisms of carbon storage in grassland soils

On a sequence of soils developed under similar vegetation, temperature, and precipitation conditions, but with variations in mineralogical properties, we use organic carbon and 14C inventories to examine mineral protection of soil organic carbon. In these soils, 14C data indicate that the creation of slow-cycling carbon can be modeled as occurring through reaction of organic ligands with Al3+ and Fe3+ cations in the upper horizons, followed by sorption to amorphous inorganic Al compounds at depth. Only one of these processes, the chelation Al3+ and Fe3+ by organic ligands, is linked to large carbon stocks. Organic ligands stabilized by this process traverse the soil column as dissolved organic carbon (both from surface horizons and root exudates). At our moist grassland site, this chelation and transport process is very strongly correlated with the storage and long-term stabilization of soil organic carbon. Our 14C results show that the mechanisms of organic carbon transport and storage at this site follow a classic model previously believed to only be significant in a single soil order (Spodosols), and closely related to the presence of forests. The presence of this process in the grassland Alfisol, Inceptisol, and Mollisol soils of this chronosequence suggests that this process is a more significant control on organic carbon storage than previously thought. Copyright 2004 by the American Geophysical Union.

Global Biogeochemical Cycles↗

USGS2007

The role of historical fire disturbance in the carbon dynamics of the pan-boreal region: A process-based analysis

[1] Wildfire is a common occurrence in ecosystems of northern high latitudes, and changes in the fire regime of this region have consequences for carbon feedbacks to the climate system. To improve our understanding of how wildfire influences carbon dynamics of this region, we used the process-based Terrestrial Ecosystem Model to simulate fire emissions and changes in carbon storage north of 45°N from the start of spatially explicit historically recorded fire records in the twentieth century through 2002, and evaluated the role of fire in the carbon dynamics of the region within the context of ecosystem responses to changes in atmospheric CO 2 concentration and climate. Our analysis indicates that fire plays an important role in interannual and decadal scale variation of source/sink relationships of northern terrestrial ecosystems and also suggests that atmospheric CO 2 may be important to consider in addition to changes in climate and fire disturbance. There are substantial uncertainties in the effects of fire on carbon storage in our simulations. These uncertainties are associated with sparse fire data for northern Eurasia, uncertainty in estimating carbon consumption, and difficulty in verifying assumptions about the representation of fires that occurred prior to the start of the historical fire record. To improve the ability to better predict how fire will influence carbon storage of this region in the future, new analyses of the retrospective role of fire in the carbon dynamics of northern high latitudes should address these uncertainties.

Journal of Geophysical Research G: Biogeosciences↗

USGS2009

Measurement of soil carbon oxidation state and oxidative ratio by 13 C nuclear magnetic resonance

The oxidative ratio (OR) of the net ecosystem carbon balance is the ratio of net O 2 and CO 2 fluxes resulting from photosynthesis, respiration, decomposition, and other lateral and vertical carbon flows. The OR of the terrestrial biosphere must be well characterized to accurately estimate the terrestrial CO 2 sink using atmospheric measurements of changing O 2 and CO 2 levels. To estimate the OR of the terrestrial biosphere, measurements are needed of changes in the OR of aboveground and belowground carbon pools associated with decadal timescale disturbances (e.g., land use change and fire). The OR of aboveground pools can be measured using conventional approaches including elemental analysis. However, measuring the OR of soil carbon pools is technically challenging, and few soil OR data are available. In this paper we test three solid-state nuclear magnetic resonance (NMR) techniques for measuring soil OR, all based on measurements of the closely related parameter, organic carbon oxidation state (C ox ). Two of the three techniques make use of a molecular mixing model which converts NMR spectra into concentrations of a standard suite of biological molecules of known C ox . The third technique assigns C ox values to each peak in the NMR spectrum. We assess error associated with each technique using pure chemical compounds and plant biomass standards whose C ox and OR values can be directly measured by elemental analyses. The most accurate technique, direct polarization solid-state 13 C NMR with the molecular mixing model, agrees with elemental analyses to ??0.036 C ox units (??0.009 OR units). Using this technique, we show a large natural variability in soil C ox and OR values. Soil C ox values have a mean of -0.26 and a range from -0.45 to 0.30, corresponding to OR values of 1.08 ?? 0.06 and a range from 0.96 to 1.22. We also estimate the OR of the carbon flux from a boreal forest fire. Analysis of soils from nearby intact soil profiles imply that soil carbon losses associated with the fire had an OR of 1.09 1 (??0.00 3 ). Fire appears to be a major factor driving the soil C pool to higher oxidation states and lower OR values. Episodic fluxes caused by disturbances like fire may have substantially different ORs from ecosystem respiration fluxes and therefore should be better quantified to reduce uncertainties associated with our understanding of the global atmospheric carbon budget. Copyright 2009 by the American Geophysical Union.

Journal of Geophysical Research G: Biogeosciences↗

USGS2023

Aquatic carbon export and dynamics in mountain headwater streams of the western U.S.

Mountain headwater streams actively cycle carbon, receiving it from terrestrial landscapes and exporting it through downstream transport and gas exchange with the atmosphere. Although their importance is now widely recognized, aquatic carbon fluxes in headwater streams remain poorly characterized. In this study, aquatic carbon fluxes were measured in 15 mountain headwater streams and were used in a geostatistical analysis to determine how landscape characteristics influence aquatic carbon fluxes. In-stream sensors were used to measure fluorescent dissolved organic matter (fDOM) (a surrogate for dissolved organic carbon (DOC)) at a subset of sites to characterize dynamic responses to hydroclimatic events. Wetlands have a positive influence on aquatic carbon fluxes, whereas perennial snow/ice has the opposite effect, reflecting differences in soil organic matter content in these landscapes. Mean annual temperature (MAT) has a complex influence on DOC, with peak DOC exports in basins with MAT of 0–2°C. Precipitation has a strong positive influence on aquatic carbon fluxes, and declining snowpacks in the western United States may reduce future aquatic carbon exports. fDOM (and by implication DOC) and

Journal of Geophysical Research: Biogeosciences.↗

USGS2024

Vegetation loss following vertical drowning of Mississippi River deltaic wetlands leads to faster microbial decomposition and decreases in soil carbon

Wetland ecosystems hold nearly a third of the global soil carbon pool, but as wetlands rapidly disappear the fate of this stored soil carbon is unclear. The aim of this study was to quantify and then link potential rates of microbial decomposition after vertical drowning of vegetated tidal marshes in coastal Louisiana to known drivers of anaerobic decomposition altered by vegetation loss. Profiles of potential CH 4 and CO 2 production (surface to 60 cm deep) were measured during anaerobic incubations, organic matter chemistry was assessed with infrared spectroscopy, and soil porewater nutrients and redox potentials were measured in the field along a chronosequence of wetland loss. After vertical drowning, pond soils had lower redox potentials, higher pH values, lower soil carbon and nitrogen concentrations, lower lignin: polysaccharide ratios, more NH 4 + and PO 4 3− , and higher rates of potential CO 2 release than vegetated marsh soils. Potential CH 4 production was similar in vegetated marshes and open water ponds, with depth-dependent decreases in CH 4 production as soil carbon concentrations increased. In these anoxic soils, vegetation loss exerts a primary control on decomposition rates because flooding drives sustained increases in porewater nutrient availability (NH 4 + and PO 4 3 , dissolved organic carbon) and decreases in redox potential (from −150 to −500 mV) that lead to higher potential CO 2 fluxes within a few years. Without new carbon inputs following wetland loss, the sustained decomposition in open water ponds may lead to losses of stored soil carbon and could influence global carbon budgets.

Louisiana↗

USGS2026

Hydrological control on soil redox condition and carbon loss of coastal wetland under sea-kevel rise

Coastal wetlands are critical carbon sinks with their biogeochemical and ecological functioning shaped by dynamic hydrological conditions that are increasingly influenced by climate change. A key unresolved question is how hydrologic flow, vegetation response, and rising sea levels interact to regulate soil redox condition and carbon loss in coastal wetlands. Using a field-tested hydrological–biogeochemical–ecological modeling framework, we reveal how the interplay between terrestrial groundwater discharge and tidal fluctuations generates complex groundwater flow patterns at the terrestrial–aquatic interface, and how these patterns modulate soil redox conditions, in turn influencing soil organic matter decomposition and carbon loss. Notably, rising sea levels suppress soil CO 2 emissions while reducing lateral dissolved carbon losses, thereby enhancing litter carbon sequestration under anoxic conditions. As vegetation responds to sea-level rise and carbon inputs diminish, litter carbon subsequently declines. These findings underscore a critical hydrological control on carbon cycling, advancing our understanding of coastal ecosystem resilience in a warming world.

Louisiana↗

USGS2025

Organic matter availability and the production of methane-derived dissolved organic carbon at methane seeps

Methane seeps located along continental margins and slopes export sedimentary methane and dissolved organic carbon (DOC) into the ocean. The flux of these reduced carbon molecules from the seafloor into the ocean impacts ocean chemistry and supports deep-sea life. While significant effort has been made to understand how the anaerobic oxidation of methane (AOM) regulates the release of methane from the seafloor, little is known about the production of DOC in association with AOM or its flux and fate in the ocean. We hypothesize a mechanism for methane incorporation into DOC at seeps and investigate the relationship between sediment total organic carbon (TOC) availability and the incorporation of methane-derived carbon into DOC at four methane seep regions along the Cascadia margin, with a range of microbial and thermogenic methane sources. At sites with <2.0 wt.% TOC (Hydrate Ridge and Bullseye Vent), up to 60%–80% of carbon in DOC is methane-carbon, much more than sites with >2.0 wt.% TOC (Astoria Canyon and Barkley Canyon). We attribute the greater methane contribution at the more TOC-limited sites to a greater role of AOM in the carbon cycle, whereas at the organic matter-rich sites, microbial competition for sulfate as an electron acceptor for organic matter decomposition limits AOM and hence the transfer of carbon from methane to DOC. We estimate that the global diffusive flux of methane-derived DOC from the seafloor is 0.07–10.1 Tg C/yr, contributing to the stock of DOC present in the deep ocean and/or fueling the deep-sea microbial loop.

California, Oregon, Washington↗

USGS2014

Rate of tree carbon accumulation increases continuously with tree size

Forests are major components of the global carbon cycle, providing substantial feedback to atmospheric greenhouse gas concentrations. Our ability to understand and predict changes in the forest carbon cycle—particularly net primary productivity and carbon storage - increasingly relies on models that represent biological processes across several scales of biological organization, from tree leaves to forest stands. Yet, despite advances in our understanding of productivity at the scales of leaves and stands, no consensus exists about the nature of productivity at the scale of the individual tree, in part because we lack a broad empirical assessment of whether rates of absolute tree mass growth (and thus carbon accumulation) decrease, remain constant, or increase as trees increase in size and age. Here we present a global analysis of 403 tropical and temperate tree species, showing that for most species mass growth rate increases continuously with tree size. Thus, large, old trees do not act simply as senescent carbon reservoirs but actively fix large amounts of carbon compared to smaller trees; at the extreme, a single big tree can add the same amount of carbon to the forest within a year as is contained in an entire mid-sized tree. The apparent paradoxes of individual tree growth increasing with tree size despite declining leaf-level and stand-level productivity can be explained, respectively, by increases in a tree’s total leaf area that outpace declines in productivity per unit of leaf area and, among other factors, age-related reductions in population density. Our results resolve conflicting assumptions about the nature of tree growth, inform efforts to understand and model forest carbon dynamics, and have additional implications for theories of resource allocation and plant senescence.

Nature↗

USGS2026

Tidal wetland soil carbon accumulation rates for coastal California

Carbon stock and carbon accumulation rate data are vital to multiple aspects of tidal wetland conservation and restoration policy. In California, USA tidal soil data are rare outside of the San Francisco Bay and Sacramento Delta regions, despite the differing conditions experienced by the outer coastline. Here we provide carbon stocks and decadal-to-centennial-scale carbon accumulation rate calculations. This dataset presents 83 soil depth profiles from 15 sites, with 58 cores from 12 tidal wetland sites analyzed for carbon stock, mostly from the outer coastline of California. Mean organic matter content was 11%, and stocks estimated to 1 meter depth ranged from 15.4 to 44.7 kgC m −2 . Organic matter content generally declined asymptotically with depth. Carbon accumulation rates ranged from 39.2 to 130.0 gC m −2 yr −1 . Neither carbon stock nor carbon accumulation rates were notably different from global average values. Data at this level of reporting are vital for establishing restoration baselines, informing greenhouse gas mitigation planning, and projecting future ecosystem response to sea-level rise.

California↗

USGS2023

Past permafrost dynamics can inform future permafrost carbon-climate feedbacks

Climate warming threatens to destabilize vast northern permafrost areas, potentially releasing large quantities of organic carbon that could further disrupt the climate. Here we synthesize paleorecords of past permafrost-carbon dynamics to contextualize future permafrost stability and carbon feedbacks. We identify key landscape differences between the last deglaciation and today that influence the response of permafrost to atmospheric warming, as well as landscape-level differences that limit subsequent carbon uptake. We show that the current magnitude of thaw has not yet exceeded that of previous deglaciations, but that permafrost carbon release has the potential to exert a strong feedback on future Arctic climate as temperatures exceed those of the Pleistocene. Better constraints on the extent of subsea permafrost and its carbon pool, and on carbon dynamics from a range of permafrost thaw processes, including blowout craters and megaslumps, are needed to help quantify the future permafrost-carbon-climate feedbacks.

Communications Earth and Environment↗

USGS2016

Biomass offsets little or none of permafrost carbon release from soils, streams, and wildfire: an expert assessment

As the permafrost region warms, its large organic carbon pool will be increasingly vulnerable to decomposition, combustion, and hydrologic export. Models predict that some portion of this release will be offset by increased production of Arctic and boreal biomass; however, the lack of robust estimates of net carbon balance increases the risk of further overshooting international emissions targets. Precise empirical or model-based assessments of the critical factors driving carbon balance are unlikely in the near future, so to address this gap, we present estimates from 98 permafrost-region experts of the response of biomass, wildfire, and hydrologic carbon flux to climate change. Results suggest that contrary to model projections, total permafrost-region biomass could decrease due to water stress and disturbance, factors that are not adequately incorporated in current models. Assessments indicate that end-of-the-century organic carbon release from Arctic rivers and collapsing coastlines could increase by 75% while carbon loss via burning could increase four-fold. Experts identified water balance, shifts in vegetation community, and permafrost degradation as the key sources of uncertainty in predicting future system response. In combination with previous findings, results suggest the permafrost region will become a carbon source to the atmosphere by 2100 regardless of warming scenario but that 65%–85% of permafrost carbon release can still be avoided if human emissions are actively reduced.

Environmental Research Letters↗

USGS2013

Modeling the effects of fire severity and climate warming on active layer and soil carbon dynamics of black spruce forests across the landscape in interior Alaska

There is a substantial amount of carbon stored in the permafrost soils of boreal forest ecosystems, where it is currently protected from decomposition. The surface organic horizons insulate the deeper soil from variations in atmospheric temperature. The removal of these insulating horizons through consumption by fire increases the vulnerability of permafrost to thaw, and the carbon stored in permafrost to decomposition. In this study we ask how warming and fire regime may influence spatial and temporal changes in active layer and carbon dynamics across a boreal forest landscape in interior Alaska. To address this question, we (1) developed and tested a predictive model of the effect of fire severity on soil organic horizons that depends on landscape-level conditions and (2) used this model to evaluate the long-term consequences of warming and changes in fire regime on active layer and soil carbon dynamics of black spruce forests across interior Alaska. The predictive model of fire severity, designed from the analysis of field observations, reproduces the effect of local topography (landform category, the slope angle and aspect and flow accumulation), weather conditions (drought index, soil moisture) and fire characteristics (day of year and size of the fire) on the reduction of the organic layer caused by fire. The integration of the fire severity model into an ecosystem process-based model allowed us to document the relative importance and interactions among local topography, fire regime and climate warming on active layer and soil carbon dynamics. Lowlands were more resistant to severe fires and climate warming, showing smaller increases in active layer thickness and soil carbon loss compared to drier flat uplands and slopes. In simulations that included the effects of both warming and fire at the regional scale, fire was primarily responsible for a reduction in organic layer thickness of 0.06 m on average by 2100 that led to an increase in active layer thickness of 1.1 m on average by 2100. The combination of warming and fire led to a simulated cumulative loss of 9.6 kgC m −2 on average by 2100. Our analysis suggests that ecosystem carbon storage in boreal forests in interior Alaska is particularly vulnerable, primarily due to the combustion of organic layer thickness in fire and the related increase in active layer thickness that exposes previously protected permafrost soil carbon to decomposition.

Alaska↗

USGS2007

Hydrogeology and paths of flow in the carbonate bedrock aquifer, northwestern Indiana

The U.S. Geological Survey (USGS) is assessing the ground.water resources of the carbonate bedrock aquifers in Indiana and Ohio as part of their Regional Aquifer Systems Analysis program. Part of this assessment includes the determination of unknown aspects of the hydraulic characteristics, boundaries, and flow paths of the carbonate aquifer. To accomplish this, the USGS drilled three wells through the carbonate aquifer near the Kankakee River in northwestern Indiana. Geophysical logs were used to help determine depths and thicknesses for testing and to help describe geology at the three wells. Packer tests were used to determine direction of ground-water flow and to provide data for an analysis of the distribution of transmissivity in the carbonate aquifer. Transmissivity of the carbonates is associated with two physical characteristics of the rocks: fractures and interconnected porosity. Almost all of the transmissivity is derived from horizontal fracturing; however, only a few of the fractures present in the carbonate are transmissive. Some transmissivity is associated with a zone of fossiliferous, vuggy dolomite, which yields water from the rock matrix. Most of the transmissivity is associated with large fractures and solution crevices in the upper 30 feet of the bedrock; less transmissivity is associated with the deeper vuggy reef material, even where extensively fractured. Transmissivity of individual fractures and fossiliferous zones ranges from 300 to 27,000 feet squared per day. The aquifer bottom is defined by a lack of transmissive fractures and an increased shale content near the contact of the Silurian and Ordovician sections. Water-level data from the three wells indicate that flow is horizontal at well site 1 north of the Kankakee River, upward at well site 2 near the river, and downward at well site 3 south of the river. Most of the flow occurs in the upper part of the carbonate bedrock where fracturing and solution-enlarged crevices are most developed. Water levels indicate the the Kankakee River is a hydrologic boundary for the regional carbonate bedrock aquifer.

Indiana↗

USGS1987

Possible Late Middle Ordovician organic carbon isotope excursion: Evidence from Ordovician oils and hydrocarbon source rocks, mid-continent and east-central United States

Oils generated by Middle Ordovician rocks are found throughout the Mid-Continent and east-central regions of the United States. Gas chromatographic characteristics of these oils include a relatively high abundance of n-alkanes with carbon numbers less than 20, a strong predominance of odd-numbered n-alkanes between C 10 and C 20 , and relatively small amounts of branched and cyclic alkanes. Saturated and aromatic hydrocarbon fractions of 43 Ordovician oils from the Anadarko, Ardmore, Forest City, Illinois, Michigan, Salina-Sedgwick, and Williston basins and the Iowa shelf demonstrate a wide range in carbon isotope composition (^dgr 13 C sat = -24.9 ^pmil to -33.9 ^pmil, (^dgr 13 C arom = -24.3 ^pmil to -33.7 ^pmil). Saturated and aromatic hydrocarbons extracted from late Middle Ordovician shales (17 core samples) show ranges in ^dgr 13 C similar to that of the oils. The wide ranges in ^dgr 13 C for oils and rock extracts reflect a major, positive excursion(s) (6-9 per ^pmil) in organic matter ^dgr 13 C in late Middle Ordovician rocks. This excursion has at least a regional significance in that it can be documented in sections 480 mi (770 km) apart in south-central Kansas and eastern Iowa. The distance may be as much as 930 mi (1,500 km) if the carbon isotope variations observed in Michigan basin Ordovician oils and in organic matter from late Middle Ordovician rocks in southwestern Ontario are related to the same carbon isotope excursion. Organic-matter ^dgr 13 C in core samples from south-central Kansas and eastern Iowa is not directly related to variations in quantity or quality of organic matter, or maceral compositi n. The positive excursion in organic matter ^dgr 13 C is a possible result of increased organic matter productivity and/or preservation. The parallel shifts in organic and carbonate ^dgr 13 C in core samples from 1 E. M. Greene well, Washington County, Iowa, imply changes in the isotope composition of the ocean-atmosphere carbon reservoir. Differences in the magnitude of the carbon isotope shifts between organic matter (8.8 ^pmil) and carbonate (4.2 ^pmil) in this core suggest a decrease, either locally or regionally, in available dissolved CO 2 , possibly a result of high organic-matter productivity and/or limited circulation in the late Middle Ordovician seas.

American Association of Petroleum Geologists Bulle↗

USGS2010

Correlation of aptian-albian carbon isotope excursions in continental strata of the cretaceous Foreland Basin, Eastern Utah, U.S.A.

Nodular carbonates ("calcretes") in continental foreland-basin strata of the Early Cretaceous Cedar Mountain Formation (CMF) in eastern Utah yield ??13C and ??O records of changes in the exogenic carbon cycle related to oceanic anoxic events (OAEs), and terrestrial paleoclimate. Chemostratigraphic profiles of both forebulge and foredeep sections show two prominent positive ??13C excursions, each with a peak value of -3% VPDB, and having background ??13C values of about -6% VPDB. These excursions correlate with the global early Aptian (Ap7) and late Aptian-early Albian (Apl2-All) carbon isotope excursions. Aptian-Albian positive ??13C excursions in the CMF also correspond to 3-4 per mil increases in carbonate ??18O. These phenomena record local aridification events. The chemostratigraphic profile on the thinner forebulge section of the CMF is calibrated, for the first time, by a radiogenic U-Pb date of 119.4 ?? 2.6 Ma on a carbonate bed, and by detrital zircon U-Pb dates on two bounding sandstone units (maximum depositional ages of 146 Ma and 112 Ma). P??trographie observations and diagenetic analyses of micritic to microsparitic carbonates from nodules indicate palustrine origins and demonstrate that they crystallized in shallow early meteoric phreatic environments. Meteoric calcite lines derived from CMF carbonates have ??18O values ranging between -8.1 to -7.5%o VPDB, supporting an estimate of zonal mean groundwater ??18O of -6% VSMOW for an Aptian-Albian paleolatitude of 34?? N. Furthermore, our two chemostratigraphic profiles exhibit a generally proportionate thinning of correlative strata from the foredeep on to the forebulge, suggesting that there were consistently lower rates of accumulation on the forebulge during the Aptian-Albian. Identification of the global Aptian-Albian ??13C excursions in purely continental strata, as demonstrated in this paper, opens a new avenue of research by identifying specific stratigraphie intervals that record the terrestrial paleoclimatic impacts of perturbations of the global carbon cycle. Copyright ?? 2010, SEPM (Society for Sedimentary Geology).

Journal of Sedimentary Research↗