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USGS2019

Sediment and organic carbon transport and deposition driven by internal tides along Monterey Canyon, offshore California

Submarine canyons provide globally important conduits for sediment and organic carbon transport into the deep-sea. Using a novel dataset from Monterey Canyon, offshore central California, that includes an extensive array of water column sampling devices, we address how fine-grained sediment and organic carbon are transported, mixed, fractionated, and buried along a submarine canyon. Anderson-type sediment traps were deployed 10 to 300 meters above the seafloor on moorings anchored between 278–1849 m water depths along the axial channel of Monterey Canyon during three consecutive 6-month deployments (2015–2017). Tidal currents within the canyon suspended and transported fine-grained sediment and organic carbon that were captured in sediment traps, which show apparent patterns and composition of sediment and organic carbon transport along the canyon. High sediment accumulation rates in traps increased up-canyon and near the seafloor with fine-scale (<1 cm) layering that was increasingly distinctive in CT scans. There was no along-canyon trend in the organic carbon composition (percent modern carbon and isotopic signatures) among trap locations, suggesting mixing. Organic carbon content (weight percent total organic carbon) and excess 210Pb activities (dpm/g) increased down-canyon, reflecting reduced flux of sediment and organic carbon into traps. Differing organic carbon signatures in traps compared with previous measurements of seabed deposits along Monterey Canyon suggest that canyon deposits may not reflect organic carbon available to organisms and transported through the canyon with internal tides. Organic carbon burial efficiency estimates from comparing core and trap samples are low (~26% or much less), suggesting that the modern upper Monterey Canyon may not be an effective sink for carbon in biogeochemical and CO2 cycling. Organic carbon isotopic signatures appear more marine in traps that sample from the water column than in cores that sample seafloor deposits, likely owing to the influence of sediment density flow events on deposits and preferential consumption of relatively fresh marine organic carbon on the seafloor that was largely prevented in preserved traps. Along-canyon sediment and organic carbon transport by internal tides likely occurs in many modern global submarine canyons, but canyon deposits and remaining organic carbon appear to preferentially reflect episodic sediment density flow events unrelated to internal tides. This study provides a quantified example and conceptual schematic for internal-tide-related sediment and organic carbon transport, mixing, and burial trends along a submarine canyon that are likely to have common global aspects.

California↗

USGS2023

Triple oxygen isotope compositions of globally distributed soil carbonates record widespread evaporation of soil waters

The stable isotopic composition of pedogenic carbonates is central to many studies of past climate and topography, providing a basis for our understanding of Earth's terrestrial history. A core assumption of many applications of oxygen isotope values (δ18O) of pedogenic carbonate is that they reflect the δ18O value of precipitation (rain/snow). This assumption is violated if soil carbonates form in evaporated soil waters. In this work, we develop a means to identify evaporation in ancient soils using the triple oxygen isotope composition (16O-17O-18O) of pedogenic carbonates. Both theoretical predictions of isotope kinetics during evaporation and studies of triple oxygen isotopes in other geological materials show that the deviation in the relationship between δ17O and δ18O from a reference line, evaluated using the parameter Δ'17O, is sensitive to evaporation. As a first step in developing the use of Δ'17O in ancient pedogenic carbonates, we report Δ'17O values from 47 near-modern pedogenic carbonate samples from globally distributed environments that vary in aridity (hyper-arid to humid). The Δ'17O values of pedogenic carbonate range from -154 to -60 per meg (as CaCO3, measured via O2, VSMOW-SLAP), corresponding to calculated soil water values of -66 to +27 per meg (VSMOW-SLAP) (using a carbonate-water triple oxygen isotope fractionation exponent of 0.5250 and clumped isotope-derived carbonate growth temperatures). The Δ'17O values indicate that evaporative modification of soil water from which pedogenic carbonate forms is common, especially in arid environments. Arid environments host pedogenic carbonates formed from soil waters ranging from highly to minimally evaporated, while humid environments host pedogenic carbonates formed from waters that are only minimally evaporated. The variability in Δ'17O within environments classified by the same aridity may relate to the fact that pedogenic carbonates record soil conditions only during times of carbonate mineralization, which may deviate from annual conditions. Thus, Δ'17O may be useful in understanding the specific circumstances of pedogenic carbonate formation but may not provide incontrovertible evidence of the magnitude of environmental aridity. Evaporative modification of δ18O values of pedogenic carbonates can be detected with Δ'17O, thereby improving estimates of δ18O of unevaporated waters. Our data show that evaporation must be (re)considered for all paleoclimate inferences based on the δ18O of pedogenic carbonate. The addition of Δ'17O will re-energize paleoclimate studies that use (or have avoided using) δ18O of pedogenic carbonate.

Geochimica et Cosmochimica Acta↗

USGS2021

Helium-carbon systematics of groundwaters in the Lassen Peak Region

Carbon dioxide emissions from active subaerial volcanoes represent 20–50% of the annual global volcanic CO 2 flux (Barry et al., 2014). Passive degassing of carbon from the flanks of volcanoes, and the associated accumulation of dissolved inorganic carbon (DIC) within nearby groundwater, also represents a potentially important, yet poorly constrained flux of carbon to the surface (Werner et al., 2019). Here we investigate sources and sinks of DIC in groundwaters in the Lassen Peak region of California. Specifically, we report and interpret the relative abundance and isotopic composition of helium ( 3 He, 4 He) and carbon ( 12 C, 13 C, 14 C) in 37 groundwater samples, from 24 distinct wells, collected between 20 and 60 km from Lassen Peak. Measured groundwater samples have air-corrected 3 He/ 4 He values between 0.19 and 7.44 R A (where R A = air 3 He/ 4 He = 1.39 × 10 −6 ), all in excess of the radiogenic production value (~0.05 R A ), indicating pervasive mantle-derived helium additions to the groundwater system in the Lassen Peak region. Stable carbon isotope ratios of DIC (δ 13 C) vary between −12.6 and − 27.7‰ (vs. VPDB). Measured groundwater DIC/ 3 He values fall in the range of 2.2 × 10 10 to 1.1 × 10 12 . Using helium and carbon isotope data, we explore several conceptual models to estimate surface carbon contributions and to differentiate between DIC derived from soil CO 2 versus DIC derived from external (slab and mantle) carbon sources. Specifically, if we use 14 C to identify soil-derived DIC (assuming decadal-to-centennial groundwater ages and a soil CO 2 14 C activity equal to that of the atmosphere), we calculate that a hypothetical external carbon source would have an apparent δ 13 C signature between −10.3 and − 59.3‰ (vs. Vienna Pee Dee Belemnite (VPDB)) and an apparent C/ 3 He between 7.0 × 10 9 and 1.0 × 10 12 . These apparent δ 13 C and C/ 3 He values are substantially isotopically lighter than and greater than canonical MORB values, respectively. We suggest that >95% of any external (non-soil-derived) DIC in groundwater must thus be non-mantle in origin (i.e., slab derived or assimilated organic carbon). We further investigate possible sources of external DIC to groundwater using two idealized conceptual approaches: a pure (unfractionated) source mixing model (after Sano and Marty, 1995) and a scenario that invokes fractionation due to calcite precipitation. Because the former model requires carbon contributions from an organic source component with unrealistically low δ 13 C (~ − 60‰), we suggest that the second scenario is more plausible. Importantly, however, we caution that all conceptual models are dependent on assumptions about initial 14 C activity. Thus, we cannot rule out the possibility that the true fraction of non-surface-derived DIC in these samples is lower or negligible, despite the pervasive mantle-derived He isotope signatures throughout the region. Following the 14 C approach to deconvolving sources of DIC, we determine that the maximum passive carbon flux could be up to ~2.2 × 10 6 kg/yr, which is lower than previous magmatic carbon flux estimates from the Lassen region (Rose and Davisson, 1996). We find that the passive dissolved carbon flux could represent a maximum of ~4–18% of the total Lassen geothermal CO 2 degassing flux (estimated to be ~3.5 × 10 7 kg/yr Rose and Davisson, 1996; Gerlach et al., 2008), which is still more than an order of magnitude smaller than soil gas CO 2 flux estimates (7.3–11 × 10 7 kg/yr) for nearby volcanoes (Sorey et al., 1998; Gerlach et al., 1999; Evans et al., 2002; Werner et al., 2014 ). We conclude that passive dissolved carbon fluxes should be combined with geothermal fluxes and soil gas fluxes to obtain a complete picture of volcanic carbon emissions globally. Our approach highlights the utility of measuring helium isotopes in concert with the full suite of noble gas abundances, tritium, δ 13 C and 14 C, which when interpreted together can be used to better elucidate the various sources of DIC in groundwater.

California↗

USGS2022

Active forest management accelerates carbon storage in plantation forests in Lishui, southern China

Background China has committed to achieving peak CO 2 emissions before 2030 and carbon neutrality before 2060; therefore, accelerated efforts are needed to better understand carbon accounting in industry and energy fields as well as terrestrial ecosystems. The carbon sink capacity of plantation forests contributes to the mitigation of climate change. Plantation forests throughout the world are intensively managed, and there is an urgent need to evaluate the effects of such management on long-term carbon dynamics. Methods We assessed the carbon cycling patterns of ecosystems characterized by three typical plantation species (Chinese fir ( Cunninghamia lanceolata (Lamb.) Hook.), oak ( Cyclobalanopsis glauca (Thunb.) Oerst.), and pine ( Pinus massoniana Lamb.)) in Lishui, southern China, by using an integrated biosphere simulator (IBIS) tuned with localized parameters. Then, we used the state-and-transition simulation model (STSM) to study the effects of active forest management (AFM) on carbon storage by combining forest disturbance history and carbon cycle regimes. Results 1) The carbon stock of the oak plantation was lower at an early age (<50 years) but higher at an advanced age (>50 years) than that of the Chinese fir and pine plantations. 2) The carbon densities of the pine and Chinese fir plantations peaked at 70 years (223.36 Mg·ha ‒1 ) and 64 years (232.04 Mg·ha ‒1 ), respectively, while the carbon density in the oak plantation continued increasing (>100 years). 3) From 1989 to 2019, the total carbon pools of the three plantation ecosystems followed an upward trend (an annual increase of 0.16–0.22 Tg C), with the largest proportional increase in the aboveground biomass carbon pool. 4) AFM increased the recovery of carbon storage after 1996 and 2009 in the pine and Chinese fir plantations, respectively, but did not result in higher growth in the oak plantation. 5) The proposed harvest planning is reasonable and conducive to maximizing the carbon sequestration capacity of the forest. Conclusions This study provides an example of a carbon cycle coupling model that is potentially suitable for simulating China's plantation forest ecosystems and supporting carbon accounting to monitor peak CO 2 emissions and reach carbon neutrality.

Lishui↗

USGS2021

Development and application of surrogate models, calculated loads, and aquatic export of carbon based on specific conductance, Big Cypress National Preserve, south Florida, 2015–17

Understanding the carbon transport within aquatic environments is crucial to quantifying global and local carbon budgets, yet limited empirical data currently (2021) exist. This report documents methodology and provides data for quantifying the aquatic export of carbon from a cypress swamp within Big Cypress National Preserve and is part of a larger carbon budget study. The U.S. Geological Survey operated two continuous monitoring stations, 022889001 and 022909471, that measured flow volume and water quality within the Big Cypress National Preserve in South Florida from September 2015 to October 2017. Station 022889001 represented the flow into the study area and station 022909471 represented the flow out of the study area. Site-specific regression models were developed by using continuously measured specific conductance and concomitant, discretely collected dissolved organic carbon, dissolved inorganic carbon, and particulate carbon samples to calculate total carbon (TC) concentrations at 15-minute intervals. Calculated TC concentrations typically increased as flow was decreasing and decreased as flow was increasing. TC loads were calculated by multiplying concentrations and flow volume, and the difference between the load calculations for input/output locations of the swamp flow system was used to determine the aquatic carbon export from the study area. Calculated monthly TC loads ranged from 0 metric tons in spring 2017 at both stations to 3,145 and 7,821 metric tons in September 2017 at 022889001 and 022909471, respectively. During 2016, the annual loads were 10,479 and 15,243 metric tons at 022889001 and 022909471, respectively. Calculated monthly aquatic TC exports from the study area ranged from −0.7 gram of carbon per square meter in May 2016 to 44.1 grams of carbon per square meter during September 2017. The carbon export from the study area varied monthly, increased as flow increased, and was greatly influenced by Hurricane Irma in September 2017. The aquatic TC export from the Sweetwater Strand study area was 42.0 grams of carbon per square meter per year in 2016, which is substantially (about 15 times) larger than the estimated overall mean riverine carbon export per square meter for the eastern United States; however, it was also less than the monthly export of carbon in September 2017. The monthly aquatic carbon export from the study area in September 2017 alone was greater than the aquatic carbon export from all of 2016, which is largely the result of the substantial increase in flow attributed to Hurricane Irma.

Florida↗

USGS2024

Distribution of ancient carbon in groundwater and soil gas from degradation of petroleum near the Red Hill Bulk Fuel Storage Facility, O‘ahu, Hawai‘i

The groundwater below the Red Hill Bulk Fuel Storage Facility (the facility) in Oʻahu, Hawaiʻi, contains fuel compounds from past spills. This study used carbon-14 analyses to distinguish fuel-derived carbon from background carbon, along with other biodegradation indicators, to address two goals: (1) determine the extent and migration direction of groundwater affected by residual fuel below the facility and (2) determine if residual fuel locations in the subsurface could be identified by analyzing soil gas at the surface above the facility. Groundwater from 19 wells was sampled between September 2022 and April 2023. Nonvolatile dissolved organic carbon (NVDOC) from a well presumed to be unaffected by past spills contained 38 percent ancient carbon indicating a natural source of ancient carbon in the subsurface. The NVDOC concentrations and ancient carbon percentages indicate fuel biodegradation products are likely present on the north and south of Red Hill with the greatest effects at well RHMW02 near the 2014 spill site. The NVDOC concentrations are almost three times higher than diesel range organic (DRO) concentrations in groundwater from the same sites. Major ion data indicate that iron reduction is an important biodegradation process. Soil probe samples and soil carbon traps were used to determine the carbon-14 content of soil carbon dioxide. Ancient carbon from fuel biodegradation was not detected at any soil probe or carbon trap site in contrast to a 2017 study which reported ancient carbon detections. A reanalysis of the 2017 results using a range of local values for background carbon-14 indicates that ancient carbon from fuel biodegradation was probably only detected in lower tunnel exhaust system samples and not in any soil carbon trap samples. Measurements of carbon dioxide efflux with a dynamic closed chamber were highly variable. The soil gas results indicate that soil gas measurements at land surface were not useful for detecting residual fuel at the facility.

Hawaii↗

USGS1998

Dissolved organic carbon concentrations and compositions, and trihalomethane formation potentials in waters from agricultural peat soils, Sacramento-San Joaquin Delta, California; implications for drinking-water quality

Water exported from the Sacramento-San Joaquin River delta (Delta) is an important drinking-water source for more than 20 million people in California. At times, this water contains elevated concentrations of dissolved organic carbon and bromide, and exceeds the U.S. Environmental Protection Agency's maximum contaminant level for trihalomethanes of 0.100 milligrams per liter if chlorinated for drinking water. About 20 to 50 percent of the trihalomethane precursors to Delta waters originates from drainage water from peat soils on Delta islands. This report elucidates some of the factors and processes controlling and affecting the concentration and quality of dissolved organic carbon released from peat soils and relates the propensity of dissolved organic carbon to form trihalomethanes to its chemical composition. Soil water was sampled from near-surface, oxidized, well-decomposed peat soil (upper soil zone) and deeper, reduced, fibrous peat soil (lower soil zone) from one agricultural field in the west central Delta over 1 year. Concentrations of dissolved organic carbon in the upper soil zone were highly variable, with median concentrations ranging from 46.4 to 83.2 milligrams per liter. Concentrations of dissolved organic carbon in samples from the lower soil zone were much less variable and generally slightly higher than samples from the upper soil zone, with median concentrations ranging from 49.3 to 82.3 milligrams per liter. The dissolved organic carbon from the lower soil zone had significantly higher aromaticity (as measured by specific ultraviolet absorbance) and contained significantly greater amounts of aromatic humic substances (as measured by XAD resin fractionation and carbon-13 nuclear magnetic resonance analysis of XAD isolates) than the dissolved organic carbon from the upper soil zone. These results support the conclusion that more aromatic forms of dissolved organic carbon are produced under anaerobic conditions compared to aerobic conditions. Dissolved organic carbon concentration, trihalomethane formation potential, and ultraviolet absorbance were all highly correlated, showing that trihalomethane precursors increased with increasing dissolved organic carbon and ultraviolet absorbance for whole water samples. Contrary to the generally accepted conceptual model for trihalomethane formation that assumes that aromatic forms of carbon are primary precursors to trihalomethanes, results from this study indicate that dissolved organic carbon aromaticity appears unrelated to trihalomethane formation on a carbon-normalized basis. Thus, dissolved organic carbon aromaticity alone cannot fully explain or predict trihalomethane precursor content, and further investigation of aromatic and nonaromatic forms of carbon will be needed to better identify trihalomethane precursors.

California↗

USGS2023

Above- and belowground biomass carbon stock and net primary productivity maps for tidal herbaceous marshes of the United States

Accurate assessments of greenhouse gas emissions and carbon sequestration in natural ecosystems are necessary to develop climate mitigation strategies. Regional and national-level assessments of carbon sequestration require high-resolution data to be available for large areas, increasing the need for remote sensing products that quantify carbon stocks and fluxes. The Intergovernmental Panel on Climate Change (IPCC) provides guidelines on how to quantify carbon flux using land cover land change and biomass carbon stock information. Net primary productivity (NPP), carbon uptake, and storage in vegetation, can also be used to model net carbon sequestration and net carbon export from an ecosystem (net ecosystem carbon balance). While biomass and NPP map products for terrestrial ecosystems are available, there are currently no conterminous United States (CONUS) biomass carbon stock or NPP maps for tidal herbaceous marshes. In this study, we used peak soil adjusted vegetation index (SAVI) values, derived from Landsat 8 composites, and five other vegetation indices, plus a categorical variable for the CONUS region (Pacific Northwest, California, Northeast, Mid-Atlantic, South Atlantic-Gulf, or Everglades), to model spatially explicit aboveground peak biomass stocks in tidal marshes (i.e., tidal palustrine and estuarine herbaceous marshes) for the first time. Tidal marsh carbon conversion factors, root-to-shoot ratios, and vegetation turnover rates, were compiled from the literature and used to convert peak aboveground biomass to peak total (above- and belowground) biomass and NPP. An extensive literature search for aboveground turnover rates produced sparse and variable values; therefore, we used an informed assumption of a turnover rate of one crop per year for all CONUS tidal marshes. Due to the lack of turnover rate data, the NPP map is identical to the peak biomass carbon stock map. In reality, it is probable that turnover rate varies by region, given seasonal length differences; however, the NPP map provides the best available information on spatially explicit CONUS tidal marsh NPP. This study identifies gaps in the scientific knowledge, to support future studies in addressing this lack of turnover data. Across CONUS, average total peak biomass carbon stock in tidal marshes was 848 g C m −2 (871 g C m −2 in palustrine and 838 g C m −2 in estuarine marshes), and based on a median biomass turnover rate of 1, it is expected that the mean NPP annual flux for tidal marshes is similar (e.g., 848 g C m −2 y −1 ). Peak biomass carbon stocks in tidal marshes were lowest in the Florida Everglades region and highest in the California regions. These are the first fine-scale national maps of biomass carbon and NPP for tidal wetlands, spanning all of CONUS. These estimates of CONUS total peak biomass carbon stocks and NPP rates for tidal marshes can support regional- and national-scale assessments of greenhouse gas emissions, as well as natural resource management of coastal wetlands, as part of nature-based climate solution efforts.

Remote Sensing↗

USGS2023

Dissolved carbon export by large river systems is influenced by source area heterogeneity

Rivers and streams export inorganic and organic carbon derived from contributing landscapes and so downstream carbon fluxes are important quantitative indicators of change in ecosystem function and for the full accounting of terrestrial carbon budgets. Carbon concentration-discharge ( C-Q ) relationships in rivers provide important information about carbon source and behavior in watersheds and are useful for estimating carbon export. However, C-Q relationships are complex in large river systems because of spatial and temporal heterogeneity in carbon dynamics across the watershed and river networks. We quantified dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC) fluxes in the Upper Mississippi River basin and investigated their relationships with land cover and hydrology. The magnitude of dissolved carbon yields ranged widely among stations, 0.6–5.7 g DOC m −2 yr −1 and 2.9–11.8 g DIC m −2 yr −1 . Spatial patterns in carbon fluxes were strongly related to land cover, with agricultural sites having high DIC/low DOC exports and forested and wetland areas having the opposite. DIC was always negatively related to discharge ( Q ), while the DOC- Q relationship varied with land cover. Differential behavior of carbon across the basin resulted in Q having a weak relationship with DOC and DIC at the basin outlet. Hence, there is a need to improve understanding of headwater terrestrial-to-aquatic carbon connections in order to improve basin-to-continental-scale carbon export estimates. Our results demonstrate that quantitative understanding of carbon export by large rivers can be improved by incorporating stream network information, such as the timing, location, and source of constituent flux, rather than relying solely upon relationships between constituent behavior and seasonality or discharge at the basin outlet.

Minnesota, Wisconsin↗

USGS2014

A shift of thermokarst lakes from carbon sources to sinks during the Holocene epoch

Thermokarst lakes formed across vast regions of Siberia and Alaska during the last deglaciation and are thought to be a net source of atmospheric methane and carbon dioxide during the Holocene epoch 1,2,3,4 . However, the same thermokarst lakes can also sequester carbon 5 , and it remains uncertain whether carbon uptake by thermokarst lakes can offset their greenhouse gas emissions. Here we use field observations of Siberian permafrost exposures, radiocarbon dating and spatial analyses to quantify Holocene carbon stocks and fluxes in lake sediments overlying thawed Pleistocene-aged permafrost. We find that carbon accumulation in deep thermokarst-lake sediments since the last deglaciation is about 1.6 times larger than the mass of Pleistocene-aged permafrost carbon released as greenhouse gases when the lakes first formed. Although methane and carbon dioxide emissions following thaw lead to immediate radiative warming, carbon uptake in peat-rich sediments occurs over millennial timescales. We assess thermokarst-lake carbon feedbacks to climate with an atmospheric perturbation model and find that thermokarst basins switched from a net radiative warming to a net cooling climate effect about 5,000   years ago. High rates of Holocene carbon accumulation in 20 lake sediments (47±10 grams of carbon per square metre per year; mean±standard error) were driven by thermokarst erosion and deposition of terrestrial organic matter, by nutrient release from thawing permafrost that stimulated lake productivity and by slow decomposition in cold, anoxic lake bottoms. When lakes eventually drained, permafrost formation rapidly sequestered sediment carbon. Our estimate of about 160petagrams of Holocene organic carbon in deep lake basins of Siberia and Alaska increases the circumpolar peat carbon pool estimate for permafrost regions by over 50 per cent (ref. 6). The carbon in perennially frozen drained lake sediments may become vulnerable to mineralization as permafrost disappears 7,8,9 , potentially negating the climate stabilization provided by thermokarst lakes during the late Holocene.

Nature↗

USGS2020

Mangrove blue carbon in the face of deforestation, climate change, and restoration

Coastal wetlands have disproportionately high carbon densities, known as blue carbon, compared to most terrestrial ecosystems. Mangroves and their blue carbon stocks are at risk globally from land‐use and land‐cover change (LULCC) activities such as aquaculture, alongside biophysical disturbances such as sea‐level rise and cyclones. Global estimates of carbon emissions from mangrove loss have been previously unable to differentiate between the variable impacts of different drivers of loss. This article discusses the impacts that different LULCC activities and biophysical disturbances have on carbon stocks (biomass and soil) and greenhouse gas fluxes (CO 2 and CH 4 ). The dynamics of carbon stocks and fluxes depends on the type of LULCC; aquaculture often results in biomass and soil carbon removal, and some forms of agriculture can substantially increase methane emissions. Natural disturbances have mixed impacts on mangrove carbon; sea‐level rise will drown some mangroves and their carbon stocks but provide opportunities for new carbon accumulation, while cyclones can have immediate negative impacts on stocks but positive impacts on sequestration during recovery. Mangrove rehabilitation practices can actively restore carbon stocks and reduce greenhouse gas emissions from previous land uses. It is critical to consider the type of LULCC when estimating carbon emissions due to mangrove loss or rehabilitation. Mangrove blue carbon is now high on the international conservation policy agenda, and a better understanding of how carbon stocks and fluxes respond to anthropogenic and biophysical disturbance may provide better incentives for mangrove conservation and sustainable management.

Annual Plant Reviews↗

USGS2017

Isotopic Approach to Soil Carbonate Dynamics and Implications for Paleoclimatic Interpretations

The radiocarbon content and stable isotope composition of soil carbonate are best described by a dynamic system in which isotopic reequilibration occurs as a result of recurrent dissolution and reprecipitation. Depth of water penetration into the soil profile, as well as soil age, determines the degree of carbonate isotope reequilibration. We measured ??13C, ??18O and radiocarbon content of gravel rinds and fine (<2 mm) carbonate in soils of 3 .different ages (1000, 3800, and 6300 14 C yr B.P.) to assess the degree to which they record and preserve a climatic signal. In soils developing in deposits independently dated at 3800 and 6300 radiocarbon yr B.P., carbonate radiocarbon content above 40 cm depth suggests continual dissolution and reprecipitation, presumably due to frequent wetting events. Between 40 and 90 cm depth, fine carbonate is dissolved and precipitated as rinds that are not redissolved subsequently. Below 90 cm depth in these soils, radiocarbon content indicates that inherited, fine carbonate undergoes little dissolution and reprecipitation. In the 3800- and 6300-yr-old soils, ??13C in rind and fine carbonate follows a decreasing trend with depth, apparently in equilibrium with modern soil gas, as predicted by a diffusive model for soil CO2. ??18O also decreases with depth due to greater evaporative enrichment above 50 cm depth. In contrast, carbonate isotopes in a 1000-yr-old deposit do not reflect modern conditions even in surficial horizons; this soil has not undergone significant pedogenesis. There appears to be a lag of at least 1000 but less than 3800 yr before carbonate inherited with parent material is modified by ambient climatic conditions. Although small amounts of carbonate are inherited with the parent material, the rate of pedogenic carbonate accumulation indicates that Ca is derived primarily from eolian and rainfall sources. A model describing carbonate input and radiocarbon decay suggests that fine carbonate below 90 cm is mostly detrital (inherited) and that carbonate rinds have been forming pedogenically at a constant rate since alluvial fans were deposited.

Quaternary Research↗

USGS1979

Effects of karst and geologic structure on the circulation of water and permeability in carbonate aquifers

The results of the natural processes caused by solution and leaching of limestone, dolomite, gypsum, salt and other soluble rocks, is known as karst. Development of karst is commonly known as karstification, which may have a pronounced effect on the topography, hydrology and environment, especially where such karst features as sinkholes and vertical solution shafts extend below the land surface and intersect lateral solution passages, cavities, caverns and other karst features in carbonate rocks. Karst features may be divided into two groups: (1) surficial features that do not extend far below the surface; and (2) karst features such as sinkholes that extend below the surface and affect the circulation of water below. The permeability of the most productive carbonate aquifers is due chiefly to enlargement of fractures and other openings by circulation of water. Important controlling factors responsible for the development of karst and permeability in carbonate aquifers include: (1) climate, topography, and presence of soluble rocks; (2) geologic structure; (3) nature of underground circulation; and (4) base level. Another important factor is the condition of the surface of the carbonate rocks at the time they are exposed to meteoric water. A carbonate rock surface, with soil or relatively permeable, less soluble cover, is more favorable for initiation of karstification and solution than bare rocks. Water percolates downward through the cover to the underlying carbonate rocks instead of running off on the surface. Also, the water becomes more corrosive as it percolates through the permeable cover to the underlying carbonate rocks. Where there is no cover or the cover has been removed, the carbonate rocks become case hardened and resistant to erosion. However, in regions underlain not only by carbonate rocks but also by beds of anhydrite, gypsum and salt, such as the Hueco Plateau in southeastern New Mexico, subsurface solution may occur where water without natural acids moves down from bare rock surfaces through cracks to the beds that are more soluble than carbonate rocks. For example, in the area of Carlsbad Caverns in southeastern New Mexico, much of the water responsible for solution that formed the caverns apparently entered the groundwater system through large open fractures and did not form sinkhole topography. East of the Carlsbad Caverns, however, in the Pecos River Valley where the carbonate rocks are overlain by the less soluble Ogallala Formation of Late Tertiary age, solution began along escarpments as the Pecos River and its tributaries cut through the less soluble cover. As these escarpments retreated, sinkholes and other karst features developed. Joints or fractures are essential for initiation of downward percolation of water in compact carbonate rocks such as some Paleozoic limestone in which there is no intergranular permeability. Also joints or fractures and bedding planes may be essential in the initiation of lateral movement of water in the zone of saturation. Where conditions of recharge and discharge are favorable, groundwater may move parallel to the dip. However, the direction of movement of water in most carbonate rocks is not necessarily down dip or parallel to the dip. The general direction of movement of both surface and groundwater may be parallel to the strike in a breached anticline. Faults may restrict the lateral movement of water, especially if water-bearing beds are faulted against relatively impervious beds. Conversely, some fault may serve as avenues through which water may move as, for example, in the Cretaceous Edwards aquifer in the San Antonio area, Texas. Karst aquifers, chiefly carbonate rocks, may be placed in three groups according to water-bearing capacity. Water in aquifers of group 1 occurs chiefly in joints, fractures, and other openings that have not been enlarged by solution. The yield of wells is small. Aquifers in group 2 , with low to intermediate yields, are those in which water occurs in joints and fractures with some cavities and channels enlarged by solution. Aquifers in group 3 are those in which the yield of wells and springs range from intermediate to very large. This group includes five of the most productive aquifers in the U.S.A. The water-bearing beds of all of these productive aquifers, except the Biscayne aquifer in southeastern Florida, contain buried paleokarst in which the permeability has been reactivated and enlarged by the present circulation system.

Journal of Hydrology↗

USGS2025

American alligators (Alligator mississippiensis) as wetland ecosystem carbon stock regulators

Blue carbon refers to organic carbon sequestered by oceanic and coastal ecosystems. This stock has gained global attention as a high organic carbon repository relative to other ecosystems. Within blue carbon ecosystems, tidally influenced wetlands alone store a disproportionately higher amount of organic carbon than other blue carbon systems. North America harbors 42% of tidally influenced global wetland area, which has been identified as a critical carbon stock in the context of climate change mitigation. However, quantified associations between vertebrate biota and carbon sequestration within ecosystems are in their infancy and have been incidental, given that microbial trophic levels are thought to drive nutrient dynamics. Here, we assess the relationship between American alligator ( Alligator mississippiensis ) demography and tidally influenced wetland soil carbon stock among habitats at continental, biogeographically-relevant, and local scales. We used soil core profile data from the Smithsonian’s Coastal Carbon Network and filtered for continuous core profiles in tidally influenced wetland areas along the Gulf and Atlantic Coasts of the United States. Results indicate that American alligator presence is positively correlated with soil carbon stock across habitats within their native distribution. Further, American alligator demographic variables are positively correlated with soil carbon stock at local scales. These conclusions are concordant with previous findings that apex predators, through trophic cascade theory, play a key role in regulating soil carbon stock and that alligators are functional apex predators in carbon dynamics and a key commercialized natural resource.

Connecticut, Delaware, Florida, Georgia, Louisiana↗

USGS2023

Arctic-boreal lakes of interior Alaska dominated by contemporary carbon

Northern high-latitude lakes are critical sites for carbon processing and serve as potential conduits for the emission of permafrost-derived carbon and greenhouse gases. However, the fate and emission pathways of permafrost carbon in these systems remain uncertain. Here, we used the natural abundance of radiocarbon to identify and trace the predominant sources of methane, carbon dioxide, dissolved inorganic and organic carbon in nine lakes within the Yukon Flats National Wildlife Refuge in interior Alaska, a discontinuous permafrost region with high landscape heterogeneity and susceptibility to climate, permafrost, and hydrological changes. We find that although Yukon Flats lakes primarily process young carbon (modern to 1290 ± 60 years before present), permafrost-derived carbon is present in some of the sampled lakes and contributes, at most, 30 ± 10% of the dissolved carbon in lake surface waters. Apportionment of young carbon and legacy carbon (carbon with radiocarbon age ⩾5000 years before present) is decoupled among the dissolved inorganic and organic carbon species, with methane showing a stronger legacy signature. Our observations suggest that permafrost-thaw-related transport of carbon through Yukon Flats lacustrine ecosystems and into the atmosphere is small, and likely regulated by surficial sediments, permafrost distribution, wildfire occurrence, or masked by contemporary carbon processes. The heterogeneity of lakes across our study area and northern landscapes more broadly cautions against using any one region (e.g. Yedoma permafrost lakes) to upscale their contribution across the pan-Arctic.

Alaska↗

USGS2021

Potential role for microbial ureolysis in the rapid formation of carbonate tufa mounds

Modern carbonate tufa towers in the alkaline (~pH 9.5) Big Soda Lake (BSL), Nevada, exhibit rapid precipitation rates (exceeding 3 cm/year) and host diverse microbial communities. Geochemical indicators reveal that carbonate precipitation is, in part, promoted by the mixing of calcium-rich groundwater and carbonate-rich lake water, such that a microbial role for carbonate precipitation is unknown. Here, we characterize the BSL microbial communities and evaluate their potential effects on carbonate precipitation that may influence fast carbonate precipitation rates of the active tufa mounds of BSL. Small subunit rRNA gene surveys indicate a diverse microbial community living endolithically, in interior voids, and on tufa surfaces. Metagenomic DNA sequencing shows that genes associated with metabolisms that are capable of increasing carbonate saturation (e.g., photosynthesis, ureolysis, and bicarbonate transport) are abundant. Enzyme activity assays revealed that urease and carbonic anhydrase, two microbial enzymes that promote carbonate precipitation, are active in situ in BSL tufa biofilms, and urease also increased calcium carbonate precipitation rates in laboratory incubation analyses. We propose that, although BSL tufas form partially as a result of water mixing, tufa-inhabiting microbiota promote rapid carbonate authigenesis via ureolysis, and potentially via bicarbonate dehydration and CO 2 outgassing by carbonic anhydrase. Microbially induced calcium carbonate precipitation in BSL tufas may generate signatures preserved in the carbonate microfabric, such as stromatolitic layers, which could serve as models for developing potential biosignatures on Earth and elsewhere.

Geobiology↗

USGS2009

Endogenic carbonate sedimentation in Bear Lake, Utah and Idaho, over the last two glacial-interglacial cycles

Sediments deposited over the past 220,000 years in Bear Lake, Utah and Idaho, are predominantly calcareous silty clay, with calcite as the dominant carbonate mineral. The abundance of siliciclastic sediment indicates that the Bear River usually was connected to Bear Lake. However, three marl intervals containing more than 50% CaCO 3 were deposited during the Holocene and the last two interglacial intervals, equivalent to marine oxygen isotope stages (MIS) 5 and 7, indicating times when the Bear River was not connected to the lake. Aragonite is the dominant mineral in two of these three high-carbonate intervals. The high-carbonate, aragonitic intervals coincide with warm interglacial continental climates and warm Pacific sea-surface temperatures. Aragonite also is the dominant mineral in a carbonate-cemented microbialite mound that formed in the southwestern part of the lake over the last several thousand years. The history of carbonate sedimentation in Bear Lake is documented through the study of isotopic ratios of oxygen, carbon, and strontium, organic carbon content, CaCO 3 content, X-ray diffraction mineralogy, and HCl-leach chemistry on samples from sediment traps, gravity cores, piston cores, drill cores, and microbialites. Sediment-trap studies show that the carbonate mineral that precipitates in the surface waters of the lake today is high-Mg calcite. The lake began to precipitate high-Mg calcite sometime in the mid-twentieth century after the artificial diversion of Bear River into Bear Lake that began in 1911. This diversion drastically reduced the salinity and Mg 2+ :Ca 2+ of the lake water and changed the primary carbonate precipitate from aragonite to high-Mg calcite. However, sediment-trap and core studies show that aragonite is the dominant mineral accumulating on the lake floor today, even though it is not precipitating in surface waters. The isotopic studies show that this aragonite is derived from reworking and redistribution of shallow-water sediment that is at least 50 yr old, and probably older. Apparently, the microbialite mound also stopped forming aragonite cement sometime after Bear River diversion. Because of reworking of old aragonite, the bulk mineralogy of carbonate in bottom sediments has not changed very much since the diversion. However, the diversion is marked by very distinct changes in the chemical and isotopic composition of the bulk carbonate. After the last glacial interval (LGI), a large amount of endogenic carbonate began to precipitate in Bear Lake when the Pacific moisture that filled the large pluvial lakes of the Great Basin during the LGI diminished, and Bear River apparently abandoned Bear Lake. At first, the carbonate that formed was low-Mg calcite, but ???11,000 years ago, salinity and Mg 2+ :Ca 2+ thresholds must have been crossed because the amount of aragonite gradually increased. Aragonite is the dominant carbonate mineral that has accumulated in the lake for the past 7000 years, with the addition of high-Mg calcite after the diversion of Bear River into the lake at the beginning of the twentieth century. Copyright ?? 2009 The Geological Society of America.

Special Paper of the Geological Society of America↗

USGS1985

Rate and depth of pedogenic-carbonate accumulation in soils: Formation and testing of a compartment model.

The rate and depth of pedogenic carbonate accumulation in soils formed in Quaternary alluvium may be viewed as a theoretical problem that involves the mutual interaction of several independent and dependent soil-forming variables. We propose a model for carbonate accumulation in which the soil column is defined by a vertical sequence of 1-cm 2 -area compartments, each with a specified texture, bulk density, water-holding content, lithologic and mineralogic composition, soil-air pCO 2 , ionic strength, and temperature. On the basis of these data, rates of carbonate solubility and dissolution within a given compartment are determined. In arkosic to lithic arkosic sandy parent materials, high carbonate solubility (0.137 to 0.212 mg/ml) and the large reactive surface area of eolian calcareous dust result in rapid carbonate dissolution (0.79 to 9.92 × 10 −10 g/cm 2 /sec) that promotes rapid translocation of carbonate by infiltrating water. We derive a group of equations and use them to calculate net carbonate depletion or accumulation in a soil compartment over an interval of time as a function of the independent variables temperature and precipitation. These two variables largely determine or strongly influence soil-water balance, the external carbonate influx rate, and carbonate solubility. The carbonate distribution that our model predicts closely resembles the observed carbonate distribution in soils associated with Holocene deposits forming in arid, hyperthermic to xeric, thermic moisture-temperature regimes in southern California. This modeling indicates that with a mean carbonate influx rate of 1 × 10 −4 g/cm 2 /yr and in a semiarid, thermic climate, the maximum depression of the top of the Cca horizon is attained within only a few thousand years. In contrast, given the same influx rate, our model predicts that a noncalcareous B horizon cannot form in an arid, hyperthermic climate, a conclusion supported by field and laboratory studies of calcic soils in this climate. The influence of glacial-to-interglacial climatic changes on carbonate accumulation can be modeled by calculating latest Pleistocene soil-water balance with the aid of published estimates of full-glacial temperature and precipitation. On the basis of these modeling results, we propose that either of two types of glacial-to-interglacial climatic changes may account for the strongly bimodal, apparently polygenetic carbonate distribution that is observed in late Pleistocene soils of the eastern Mojave Desert of southern California. Such results of compartment-strategy modeling are encouraging and indicate the great potential of combined theoretical and empirical methods for considering pedological problems of interest to Quaternary geologists.

GSA Special Papers↗