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Results for “Global Biogeochemical Cycles”

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USGS2001

Budgets of soil erosion and deposition for sediments and sedimentary organic carbon across the conterminous United States

The fate of soil organic matter during erosion and sedimentation has been difficult to assess because of the large size and complex turnover characteristics of the soil carbon reservoir. It has been assumed that most of the carbon released during erosion is lost to oxidation. Budgets of bulk soil and soil organic carbon erosion and deposition suggest that the primary fates of eroded soil carbon across the conterminous United States are trapping in impoundments and other redeposition. The total amount of soil carbon eroded and redeposited across the United States is ???0.04 Gt yr-1. Applying this revision to the U. S. carbon budget by Houghton et al. [1999] raises their net sequestration estimate by 20-47 %. If comparable rates of erosion and redeposition occur globally, net carbon sequestration would be ???1 Gt yr-1.

Global Biogeochemical Cycles↗

USGS2002

Historical and future land use effects on N 2 O and NO emissions using an ensemble modeling approach: Costa Rica's Caribbean lowlands as an example

[1] The humid tropical zone is a major source area for N 2 O and NO emissions to the atmosphere. Local emission rates vary widely with local conditions, particularly land use practices which swiftly change with expanding settlement and changing market conditions. The combination of wide variation in emission rates and rapidly changing land use make regional estimation and future prediction of biogenic trace gas emission particularly difficult. This study estimates contemporary, historical, and future N 2 O and NO emissions from 0.5 million ha of northeastern Costa Rica, a well-documented region in the wet tropics undergoing rapid agricultural development. Estimates were derived by linking spatially distributed environmental data with an ecosystem simulation model in an ensemble estimation approach that incorporates the variance and covariance of spatially distributed driving variables. Results include measures of variance for regional emissions. The formation and aging of pastures from forest provided most of the past temporal change in N 2 O and NO flux in this region; future changes will be controlled by the degree of nitrogen fertilizer application and extent of intensively managed croplands.

Global Biogeochemical Cycles↗

USGS2002

A multiisotope C and N modeling analysis of soil organic matter turnover and transport as a function of soil depth in a California annual grassland soil chronosequence

We examine soil organic matter (SOM) turnover and transport using C and N isotopes in soil profiles sampled circa 1949, 1978, and 1998 (a period spanning pulse thermonuclear 14 C enrichment of the atmosphere) along a 3‐million‐year annual grassland soil chronosequence. Temporal differences in soil Δ 14 C profiles indicate that inputs of recently living organic matter (OM) occur primarily in the upper 20–30 cm but suggest that OM inputs can occur below the primary rooting zone. A three‐pool SOM model with downward transport captures most observed variation in Δ 14 C, percentages of C and N, δ 13 C, and δ 15 N, supporting the commonly accepted concept of three distinct SOM pools. The model suggests that the importance of the decadal SOM pool in N dynamics is greatest in young and old soils. Altered hydrology and possibly low pH and/or P dynamics in highly developed old soils cause changes in soil C and N turnover and transport of importance for soil biogeochemistry models.

Global Biogeochemical Cycles↗

USGS2003

Isotopic composition of carbon dioxide from a boreal forest fire: Inferring carbon loss from measurements and modeling

Fire is an important pathway for carbon (C) loss from boreal forest ecosystems and has a strong effect on ecosystem C balance. Fires can range widely in severity, defined as the amount of vegetation and forest floor consumed by fire, depending on local fuel and climatic conditions. Here we explore a novel method for estimating fire severity and loss of C from fire using the atmosphere to integrate ecosystem heterogeneity at the watershed scale. We measured the δ 13 C and Δ 14 C isotopic values of CO 2 emitted from an experimental forest fire at the Caribou-Poker Creek Research Watershed (CPCRW), near Fairbanks, Alaska. We used inverse modeling combined with dual isotope measurements of C contained in aboveground black spruce biomass and soil organic horizons to estimate the amount of C released by this fire. The experimental burn was a medium to severe intensity fire that released, on average, about 2.5 kg Cm −2 , more than half of the C contained in vegetation and soil organic horizon pools. For vegetation, the model predicted that approximately 70–75% of pools such as needles, fine branches, and bark were consumed by fire, whereas only 20–30% of pools such as coarse branches and cones were consumed. The fire was predicted to have almost completely consumed surface soil organic horizons and burned about half of the deepest humic horizon. The ability to estimate the amount of biomass combusted and C emission from fires at the watershed scale provides an extensive approach that can complement more limited intensive ground-based measurements.

Alaska↗

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↗

USGS2005

Soil organic carbon dynamics as related to land use history in the northwestern Great Plains

Strategies for mitigating the global greenhouse effect must account for soil organic carbon (SOC) dynamics at both spatial and temporal scales, which is usually challenging owing to limitations in data and approach. This study was conducted to characterize the SOC dynamics associated with land use change history in the northwestern Great Plains ecoregion. A sampling framework (40 sample blocks of 10 × 10 km 2 randomly located in the ecoregion) and the General Ensemble Biogeochemical Modeling System (GEMS) were used to quantify the spatial and temporal variability in the SOC stock from 1972 to 2001. Results indicate that C source and sink areas coexisted within the ecoregion, and the SOC stock in the upper 20-cm depth increased by 3.93 Mg ha −1 over the 29 years. About 17.5% of the area was evaluated as a C source at 122 kg C ha −1 yr −1 . The spatial variability of SOC stock was attributed to the dynamics of both slow and passive fractions, while the temporal variation depended on the slow fraction only. The SOC change at the block scale was positively related to either grassland proportion or negatively related to cropland proportion. We concluded that the slow C pool determined whether soils behaved as sources or sinks of atmospheric CO 2 , but the strength depended on antecedent SOC contents, land cover type, and land use change history in the ecoregion.

Global Biogeochemical Cycles↗

USGS2008

Sediment organic carbon burial in agriculturally eutrophic impoundments over the last century

We estimated organic carbon (OC) burial over the past century in 40 impoundments in one of the most intensively agricultural regions of the world. The volume of sediment deposited per unit time varied as a function of lake and watershed size, but smaller impoundments had greater deposition and accumulation rates per unit area. Annual water storage losses varied from 0.1-20% and were negatively correlated with impoundment size. Estimated sediment OC content was greatest in lakes with low ratios of watershed to impoundment area. Sediment OC burial rates were higher than those assumed for fertile impoundments by previous studies and were much higher than those measured in natural lakes. OC burial ranged from a high of 17,000 g C m-2 a-1 to a low of 148 g C m-2 a-1 and was significantly greater in small impoundments than large ones. The OC buried in these lakes originates in both autochthonous and allochthonous production. These analyses suggest that OC sequestration in moderate to large impoundments may be double the rate assumed in previous analyses. Extrapolation suggests that they may bury 4 times as much carbon (C) as the world's oceans. The world's farm ponds alone may bury more OC than the oceans and 33% as much as the world's rivers deliver to the sea. Copyright 2008 by the American Geophysical Union.

Global Biogeochemical Cycles↗

USGS2007

Flux and age of dissolved organic carbon exported to the Arctic Ocean: A carbon isotopic study of the five largest arctic rivers

The export and Δ 14 C-age of dissolved organic carbon (DOC) was determined for the Yenisey, Lena, Ob', Mackenzie, and Yukon rivers for 2004–2005. Concentrations of DOC elevate significantly with increasing discharge in these rivers, causing approximately 60% of the annual export to occur during a 2-month period following spring ice breakup. We present a total annual flux from the five rivers of ∼16 teragrams (Tg), and conservatively estimate that the total input of DOC to the Arctic Ocean is 25–36 Tg, which is ∼5–20% greater than previous fluxes. These fluxes are also ∼2.5× greater than temperate rivers with similar watershed sizes and water discharge. Δ 14 C-DOC shows a clear relationship with hydrology. A small pool of DOC slightly depleted in Δ 14 C is exported with base flow. The large pool exported with spring thaw is enriched in Δ 14 C with respect to current-day atmospheric Δ 14 C-CO 2 values. A simple model predicts that ∼50% of DOC exported during the arctic spring thaw is 1–5 years old, ∼25% is 6–10 years in age, and 15% is 11–20 years old. The dominant spring melt period, a historically undersampled period, exports a large amount of young and presumably semilabile DOC to the Arctic Ocean.

Global Biogeochemical Cycles↗

USGS2008

Climatically driven loss of calcium in steppe soil as a sink for atmospheric carbon

During the last several thousand years the semi-arid, cold climate of the Russian steppe formed highly fertile soils rich in organic carbon and calcium (classified as Chernozems in the Russian system). Analysis of archived soil samples collected in Kemannaya Steppe Preserve in 1920, 1947, 1970, and fresh samples collected in 1998 indicated that the native steppe Chernozems, however, lost 17-28 kg m-2 of calcium in the form of carbonates in 1970-1998. Here we demonstrate that the loss of calcium was caused by fundamental shift in the steppe hydrologic balance. Previously unleached soils where precipitation was less than potential evapotranspiration are now being leached due to increased precipitation and, possibly, due to decreased actual evapotranspiration. Because this region receives low levels of acidic deposition, the dissolution of carbonates involves the consumption of atmospheric CO2. Our estimates indicate that this climatically driven terrestrial sink of atmospheric CO2 is ???2.1-7.4 g C m-2 a-1. In addition to the net sink of atmospheric carbon, leaching of pedogenic carbonates significantly amplified seasonal amplitude of CO2 exchange between atmosphere and steppe soil. Copyright 2008 by the American Geophysical Union.

Global Biogeochemical Cycles↗

USGS2008

Seasonal and spatial variability in dissolved organic matter quantity and composition from the Yukon River basin, Alaska

[1] The seasonal and spatial variability of dissolved organic matter (DOM) quantity and chemical composition were investigated in the Yukon River basin of Alaska, United States, and northwestern Canada. Dissolved organic carbon (DOC), chromophoric DOM (CDOM), and dissolved lignin phenols were measured across a range of source waters and the seasonal hydrograph. Strong relationships were determined between CDOM and both DOC and lignin phenols, highlighting the potential for deriving detailed spatial and temporal distributions of DOM composition from CDOM monitoring. Maximum concentrations of measured parameters were observed during the spring flush, when DOM had a remarkably high content of aromatic vascular plant material derived from surface soil and litter layers. A larger portion of riverine DOM was attributed to vascular plant sources than previously believed by utilizing representative vegetation leachates and a soil pore water as end‐members. In combination with recent studies highlighting export of young, labile DOM during the spring flush in northern high‐latitude river systems, our results suggest riverine DOM is less degraded and more labile than previously thought with clear ramifications for its biomineralization or photo‐oxidation in marine environments.

Global Biogeochemical Cycles↗

USGS2009

Mercury sources, distribution, and bioavailability in the North Pacific Ocean: Insights from data and models

Fish harvested from the Pacific Ocean are a major contributor to human methylmercury (MeHg) exposure. Limited oceanic mercury (Hg) data, particularly MeHg, has confounded our understanding of linkages between sources, methylation sites, and concentrations in marine food webs. Here we present methylated (MeHg and dimethylmercury (Me 2 Hg)) and total Hg concentrations from 16 hydrographic stations in the eastern North Pacific Ocean. We use these data in combination with information from previous cruises and coupled atmospheric‐oceanic modeling results to better understand controls on Hg concentrations, distribution, and bioavailability. Total Hg concentrations (average 1.14 ± 0.38 pM) are elevated relative to previous cruises. Modeling results agree with observed increases and suggest that at present atmospheric Hg deposition rates, basin‐wide Hg concentrations will double relative to circa 1995 by 2050. Methylated Hg accounts for up to 29% of the total Hg in subsurface waters (average 260 ± 114 fM). We observed lower ambient methylated Hg concentrations in the euphotic zone and older, deeper water masses, which likely result from decay of MeHg and Me 2 Hg when net production is not occurring. We found a significant, positive linear relationship between methylated Hg concentrations and rates of organic carbon remineralization ( r 2 = 0.66, p < 0.001). These results provide evidence for the importance of particulate organic carbon (POC) transport and remineralization on the production and distribution of methylated Hg species in marine waters. Specifically, settling POC provides a source of inorganic Hg(II) to microbially active subsurface waters and can also provide a substrate for microbial activity facilitating water column methylation.

Global Biogeochemical Cycles↗

USGS2011

Strong atmospheric chemistry feedback to climate warming from Arctic methane emissions

The magnitude and feedbacks of future methane release from the Arctic region are unknown. Despite limited documentation of potential future releases associated with thawing permafrost and degassing methane hydrates, the large potential for future methane releases calls for improved understanding of the interaction of a changing climate with processes in the Arctic and chemical feedbacks in the atmosphere. Here we apply a “state of the art” atmospheric chemistry transport model to show that large emissions of CH4 would likely have an unexpectedly large impact on the chemical composition of the atmosphere and on radiative forcing (RF). The indirect contribution to RF of additional methane emission is particularly important. It is shown that if global methane emissions were to increase by factors of 2.5 and 5.2 above current emissions, the indirect contributions to RF would be about 250% and 400%, respectively, of the RF that can be attributed to directly emitted methane alone. Assuming several hypothetical scenarios of CH4 release associated with permafrost thaw, shallow marine hydrate degassing, and submarine landslides, we find a strong positive feedback on RF through atmospheric chemistry. In particular, the impact of CH4 is enhanced through increase of its lifetime, and of atmospheric abundances of ozone, stratospheric water vapor, and CO2 as a result of atmospheric chemical processes. Despite uncertainties in emission scenarios, our results provide a better understanding of the feedbacks in the atmospheric chemistry that would amplify climate warming.

Global Biogeochemical Cycles↗

USGS2012

Landscape-level controls on dissolved carbon flux from diverse catchments of the circumboreal

While much of the dissolved organic carbon (DOC) within rivers is destined for mineralization to CO 2 , a substantial fraction of riverine bicarbonate (HCO 3 - ) flux represents a CO 2 sink, as a result of weathering processes that sequester CO 2 as HCO 3 - . We explored landscape-level controls on DOC and HCO 3 - flux in subcatchments of the boreal, with a specific focus on the effect of permafrost on riverine dissolved C flux. To do this, we undertook a multivariate analysis that partitioned the variance attributable to known, key regulators of dissolved C flux (runoff, lithology, and vegetation) prior to examining the effect of permafrost, using riverine biogeochemistry data from a suite of subcatchments drawn from the Mackenzie, Yukon, East, and West Siberian regions of the circumboreal. Across the diverse catchments that we study, controls on HCO 3 - flux were near-universal: runoff and an increased carbonate rock contribution to weathering (assessed as riverwater Ca:Na) increased HCO 3 - yields, while increasing permafrost extent was associated with decreases in HCO 3 - . In contrast, permafrost had contrasting and region-specific effects on DOC yield, even after the variation caused by other key drivers of its flux had been accounted for. We used ionic ratios and SO 4 yields to calculate the potential range of CO 2 sequestered via weathering across these boreal subcatchments, and show that decreasing permafrost extent is associated with increases in weathering-mediated CO 2 fixation across broad spatial scales, an effect that could counterbalance some of the organic C mineralization that is predicted with declining permafrost.

Global Biogeochemical Cycles↗

USGS2012

Carbon dioxide and methane emissions from the Yukon River system

Carbon dioxide (CO 2 ) and methane (CH 4 ) emissions are important, but poorly quantified, components of riverine carbon (C) budgets. This is largely because the data needed for gas flux calculations are sparse and are spatially and temporally variable. Additionally, the importance of C gas emissions relative to lateral C exports is not well known because gaseous and aqueous fluxes are not commonly measured on the same rivers. We couple measurements of aqueous CO 2 and CH 4 partial pressures ( p CO 2 , p CH 4 ) and flux across the water-air interface with gas transfer models to calculate subbasin distributions of gas flux density. We then combine those flux densities with remote and direct observations of stream and river water surface area and ice duration, to calculate C gas emissions from flowing waters throughout the Yukon River basin. CO 2 emissions were 7.68 Tg C yr −1 (95% CI: 5.84 −10.46), averaging 750 g C m −2 yr −1 normalized to water surface area, and 9.0 g C m −2 yr −1 normalized to river basin area. River CH 4 emissions totaled 55 Gg C yr −1 or 0.7% of the total mass of C emitted as CO 2 plus CH 4 and ∼6.4% of their combined radiative forcing. When combined with lateral inorganic plus organic C exports to below head of tide, C gas emissions comprised 50% of total C exported by the Yukon River and its tributaries. River CO 2 and CH 4 derive from multiple sources, including groundwater, surface water runoff, carbonate equilibrium reactions, and benthic and water column microbial processing of organic C. The exact role of each of these processes is not yet quantified in the overall river C budget.

Yukon River Basin↗

USGS2012

Dissolved organic matter composition of winter flow in the Yukon River basin: Implications of permafrost thaw and increased groundwater discharge

Groundwater discharge to rivers has increased in recent decades across the circumpolar region and has been attributed to thawing permafrost in arctic and subarctic watersheds. Permafrost-driven changes in groundwater discharge will alter the flux of dissolved organic carbon (DOC) in rivers, yet little is known about the chemical composition and reactivity of dissolved organic matter (DOM) of groundwater in permafrost settings. Here, we characterize DOM composition of winter flow in 60 rivers and streams of the Yukon River basin to evaluate the biogeochemical consequences of enhanced groundwater discharge associated with permafrost thaw. DOC concentration of winter flow averaged 3.9 ± 0.5 mg C L −1 , yet was highly variable across basins (ranging from 20 mg C L −1 ). In comparison to the summer-autumn period, DOM composition of winter flow had lower aromaticity (as indicated by specific ultraviolet absorbance at 254 nm, or SUVA 254 ), lower hydrophobic acid content, and a higher proportion of hydrophilic compounds (HPI). Fluorescence spectroscopy and parallel factor analysis indicated enrichment of protein-like fluorophores in some, but not all, winter flow samples. The ratio of DOC to dissolved organic nitrogen, an indicator of DOM biodegradability, was positively correlated with SUVA 254 and negatively correlated with the percentage of protein-like compounds. Using a simple two-pool mixing model, we evaluate possible changes in DOM during the summer-autumn period across a range of conditions reflecting possible increases in groundwater discharge. Across three watersheds, we consistently observed decreases in DOC concentration and SUVA254 and increases in HPI with increasing groundwater discharge. Spatial patterns in DOM composition of winter flow appear to reflect differences in the relative contributions of groundwater from suprapermafrost and subpermafrost aquifers across watersheds. Our findings call for more explicit consideration of DOC loss and stabilization pathways associated with changing subsurface hydrology in watersheds underlain by thawing permafrost.

Global Biogeochemical Cycles↗

USGS2012

Biodegradability of dissolved organic carbon in the Yukon River and its tributaries: Seasonality and importance of inorganic nitrogen

Northern high-latitude rivers transport large amounts of terrestrially derived dissolved organic matter (DOM) from boreal and arctic ecosystems to coastal areas and oceans. Current knowledge of the biodegradability of DOM in these rivers is limited, particularly for large rivers discharging to the Arctic Ocean. We conducted a seasonally comprehensive study of biodegradable dissolved organic carbon (BDOC) dynamics in the Yukon River and two of its tributaries in Alaska, USA. Distinct seasonal patterns of BDOC, consistent across a wide range of watershed size, indicate BDOC is transported year-round. Relative biodegradability (%BDOC) was greatest during winter, and decreased into spring and summer. Due to large seasonal differences in DOC concentration, the greatest concentrations of BDOC (mg C L −1 ) occurred during spring freshet, followed by winter and summer. While chemical composition of DOM was an important driver of BDOC, the overriding control of BDOC was mineral nutrient availability due to wide shifts in carbon (C) and nitrogen (N) stoichiometry across seasons. We calculated seasonal and annual loads of BDOC exported by the Yukon River by applying measured BDOC concentrations to daily water discharge values, and also by applying an empirical correlation between %BDOC and the ratio of DOC to dissolved inorganic N (DIN) to total DOC loads. The Yukon River exports &sim;0.2 Tg C yr −1 as BDOC that is decomposable within 28 days. This corresponds to 12–18% of the total annual DOC export. Furthermore, we calculate that the six largest arctic rivers, including the Yukon River, collectively export &sim;2.3 Tg C yr −1 as BDOC to the Arctic Ocean.

Global Biogeochemical Cycles↗

USGS2018

The role of the upper tidal estuary in wetland blue carbon storage and flux

Carbon (C) standing stocks, C mass balance, and soil C burial in tidal freshwater forested wetlands (TFFW) and TFFW transitioning to low‐salinity marshes along the upper estuary are not typically included in “blue carbon” accounting, but may represent a significant C sink. Results from two salinity transects along the tidal Waccamaw and Savannah rivers of the US Atlantic Coast show total C standing stocks were 321‐1264 Mg C ha ‐1 among all sites, generally shifting to greater soil storage as salinity increased. Carbon mass balance inputs (litterfall, woody growth, herbaceous growth, root growth, surface accumulation) minus C outputs (surface litter and root decomposition, gaseous C) over a period of up to 11 years were 340‐900 g C m ‐2 yr ‐1 . Soil C burial was variable (7‐337 g C m ‐2 yr ‐1 ), and lateral C export was estimated as C mass balance minus soil C burial as 267‐849 g C m ‐2 yr ‐1 . This represents a large amount of C export to support aquatic biogeochemical transformations. Despite reduced C persistence within emergent vegetation, decomposition of organic matter, and higher lateral C export, total C storage increased as forests converted to marsh with salinization. These tidal river wetlands exhibited high N mineralization in salinity‐stressed forested sites and considerable P mineralization in low salinity marshes. Large C standing stocks and rates of C sequestration suggest that TFFW and oligohaline marshes are considerably important globally to coastal C dynamics and in facilitating energy transformations in areas of the world in which they occur.

Georgia, South Carolina↗

USGS2019

Remobilization of old permafrost carbon to Chukchi Sea sediments during the end of the last deglaciation

Climate warming is expected to destabilize permafrost carbon (PF‐C) by thaw‐erosion and deepening of the seasonally thawed active layer and thereby promote PF‐C mineralization to CO 2 and CH 4 . A similar PF‐C remobilization might have contributed to the increase in atmospheric CO 2 during deglacial warming after the last glacial maximum. Using carbon isotopes and terrestrial biomarkers (Δ 14 C, δ 13 C, and lignin phenols), this study quantifies deposition of terrestrial carbon originating from permafrost in sediments from the Chukchi Sea (core SWERUS‐L2‐4‐PC1). The sediment core reconstructs remobilization of permafrost carbon during the late Allerød warm period starting at 13,000 cal years before present (BP), the Younger Dryas, and the early Holocene warming until 11,000 cal years BP and compares this period with the late Holocene, from 3,650 years BP until present. Dual‐carbon‐isotope‐based source apportionment demonstrates that Ice Complex Deposit—ice‐ and carbon‐rich permafrost from the late Pleistocene (also referred to as Yedoma)—was the dominant source of organic carbon (66 ± 8%; mean ± standard deviation) to sediments during the end of the deglaciation, with fluxes more than twice as high (8.0 ± 4.6 g·m −2 ·year −1 ) as in the late Holocene (3.1 ± 1.0 g·m −2 ·year −1 ). These results are consistent with late deglacial PF‐C remobilization observed in a Laptev Sea record, yet in contrast with PF‐C sources, which at that location were dominated by active layer material from the Lena River watershed. Release of dormant PF‐C from erosion of coastal permafrost during the end of the last deglaciation indicates vulnerability of Ice Complex Deposit in response to future warming and sea level changes.

Global Biogeochemical Cycles↗