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At least 1,243 records · Page 69Linked to original sources

Influence of disturbance on carbon exchange in a permafrost collapse and adjacent burned forest

We measured CO 2 and CH 4 exchange from the center of a Sphagnum ‐dominated permafrost collapse, through an aquatic moat, and into a recently burned black spruce forest on the Tanana River floodplain in interior Alaska. In the anomalously dry growing season of 2004, both the collapse and the surrounding burned area were net sinks for CO 2 , with a mean daytime net ecosystem exchange of −1.4 μ mol CO 2 m −2 s −1 , while the moat was a CH 4 source with a mean flux of 0.013 μ mol CH 4 m −2 s −1 . Regression analyses identified temperature as the dominant factor affecting intragrowing season variation in CO 2 exchange and soil moisture as the primary control influencing CH 4 emissions. CH 4 emissions during the wettest portion of the growing season were four times higher than during the driest periods. If temperatures continue to warm, peatland vegetation will likely expand with permafrost degradation, resulting in greater carbon accumulation and methane emissions for the landscape as a whole.

Alaska↗

Mercury dynamics in relation to dissolved organic carbon concentration and quality during high flow events in three northeastern U.S. streams

Mercury (Hg) contamination is widespread in remote areas of the northeastern United States. Forested uplands have accumulated a large reservoir of Hg in soil from decades of elevated anthropogenic deposition that can be released episodically to stream water during high flows. The objective of this study was to evaluate spatial and temporal variations in stream water Hg species and organic matter fractions over a range of hydrologic conditions in three forested upland watersheds (United States). Mercury and organic matter concentrations increased with discharge at all three sites; however, the partitioning of Hg fractions (dissolved versus particulate) differed among sites and seasons. Associated with increased discharge, flow paths shifted from mineral soil under base flow to upper soil horizons. As flow paths shifted, greater concentrations of dissolved organic carbon (DOC) richer in aromatic substances were flushed from upper soil horizons to stream water. The hydrophobic organic matter associated with humic material from upper soils appears to have had a greater capacity to bind Hg. Because of the strong correlation between Hg and DOC, we hypothesize that there was a concurrent shift in the source of Hg with DOC from lower mineral soil to upper soil horizons. Our study suggests that stream discharge is an effective predictor of dissolved total Hg flux.

Water Resources Research↗

Hydrological mobilization of mercury and dissolved organic carbon in a snow-dominated, forested watershed: Conceptualization and modeling

The mobilization of mercury and dissolved organic carbon (DOC) during snowmelt often accounts for a major fraction of the annual loads. We studied the role of hydrological connectivity of riparian wetlands and upland/wetland transition zones to surface waters on the mobilization of Hg and DOC in Fishing Brook, a headwater of the Adirondack Mountains, New York. Stream water total mercury (THg) concentrations varied strongly (mean = 2.25 ± 0.5 ng L −1 ), and the two snowmelt seasons contributed 40% (2007) and 48% (2008) of the annual load. Methyl mercury (MeHg) concentrations ranged up to 0.26 ng L −1 , and showed an inverse log relationship with discharge. TOPMODEL‐simulated saturated area corresponded well with wetland areas, and the application of a flow algorithm based elevation‐above‐creek approach suggests that most wetlands become well connected during high flow. The dynamics of simulated saturated area and soil storage deficit were able to explain a large part of the variation of THg concentrations (r 2 = 0.53 to 0.72). In contrast, the simulations were not able to explain DOC variations and DOC and THg concentrations were not correlated. These results indicate that all three constituents, THg, MeHg, and DOC, follow different patterns at the outlet: (1) the mobilization of THg is primarily controlled by the saturation state of the catchment, (2) the dilution of MeHg suggests flushing from a supply limited pool, and (3) DOC dynamics follow a pattern different from THg dynamics, which likely results from differing gain and/or loss processes for THg and/or DOC within the Fishing Brook catchment.

New York↗

Vulnerability of high-latitude soil organic carbon in North America to disturbance

This synthesis addresses the vulnerability of the North American high-latitude soil organic carbon (SOC) pool to climate change. Disturbances caused by climate warming in arctic, subarctic, and boreal environments can result in significant redistribution of C among major reservoirs with potential global impacts. We divide the current northern high-latitude SOC pools into (1) near-surface soils where SOC is affected by seasonal freeze-thaw processes and changes in moisture status, and (2) deeper permafrost and peatland strata down to several tens of meters depth where SOC is usually not affected by short-term changes. We address key factors (permafrost, vegetation, hydrology, paleoenvironmental history) and processes (C input, storage, decomposition, and output) responsible for the formation of the large high-latitude SOC pool in North America and highlight how climate-related disturbances could alter this pool's character and size. Press disturbances of relatively slow but persistent nature such as top-down thawing of permafrost, and changes in hydrology, microbiological communities, pedological processes, and vegetation types, as well as pulse disturbances of relatively rapid and local nature such as wildfires and thermokarst, could substantially impact SOC stocks. Ongoing climate warming in the North American high-latitude region could result in crossing environmental thresholds, thereby accelerating press disturbances and increasingly triggering pulse disturbances and eventually affecting the C source/sink net character of northern high-latitude soils. Finally, we assess postdisturbance feedbacks, models, and predictions for the northern high-latitude SOC pool, and discuss data and research gaps to be addressed by future research.

Journal of Geophysical Research G: Biogeosciences↗

Volcanic versus anthropogenic carbon dioxide

Which emits more carbon dioxide (CO 2 ): Earth's volcanoes or human activities? Research findings indicate unequivocally that the answer to this frequently asked question is human activities. However, most people, including some Earth scientists working in fields outside volcanology, are surprised by this answer. The climate change debate has revived and reinforced the belief, widespread among climate skeptics, that volcanoes emit more CO 2 than human activities [ Gerlach , 2010; Plimer , 2009]. In fact, present-day volcanoes emit relatively modest amounts of CO 2 , about as much annually as states like Florida, Michigan, and Ohio.

Eos, Transactions, American Geophysical Union↗

Dissolved organic carbon and chromophoric dissolved organic matter properties of rivers in the USA

Dissolved organic carbon (DOC) concentration and chromophoric dissolved organic matter (CDOM) parameters were measured over a range of discharge in 30 U.S. rivers, covering a diverse assortment of fluvial ecosystems in terms of watershed size and landscape drained. Relationships between CDOM absorption at a range of wavelengths (a 254 , a 350 , a 440 ) and DOC in the 30 watersheds were found to correlate strongly and positively for the majority of U.S. rivers. However, four rivers (Colorado, Colombia, Rio Grande and St. Lawrence) exhibited statistically weak relationships between CDOM absorption and DOC. These four rivers are atypical, as they either drain from the Great Lakes or experience significant impoundment of water within their watersheds, and they exhibited values for dissolved organic matter (DOM) parameters indicative of autochthonous or anthropogenic sources or photochemically degraded allochthonous DOM and thus a decoupling between CDOM and DOC. CDOM quality parameters in the 30 rivers were found to be strongly correlated to DOM compositional metrics derived via XAD fractionation, highlighting the potential for examining DOM biochemical quality from CDOM measurements. This study establishes the ability to derive DOC concentration from CDOM absorption for the majority of U.S. rivers, describes characteristics of riverine systems where such an approach is not valid, and emphasizes the possibility of examining DOM composition and thus biogeochemical function via CDOM parameters. Therefore, the usefulness of CDOM measurements, both laboratory-based analyses and in situ instrumentation, for improving spatial and temporal resolution of DOC fluxes and DOM dynamics in future studies is considerable in a range of biogeochemical studies.

Journal of Geophysical Research G: Biogeosciences↗

Looking skyward to study ecosystem carbon dynamics

Between May and October 2011 the U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy's Atmospheric Radiation Measurement (ARM) program, conducted a field campaign at the ARM Southern Great Plains site in north central Oklahoma to evaluate a new instrument for quantitative image-based monitoring of sky conditions and solar radiation. The High Dynamic Range All-Sky Imaging System (HDR-ASIS) was developed by USGS to support studies of cloud- and aerosol-induced variability in the geometric properties of solar radiation (the sky radiance distribution) and its effects on photosynthesis and uptake of carbon dioxide (CO 2 ) by terrestrial ecosystems. Under a clean, cloudless atmosphere when the Sun is above the horizon, most of the solar radiation reaching an area of the Earth's surface is concentrated in a beam coming directly from the Sun; a relatively small proportion arrives as diffuse radiation from the rest of the sky. Clouds and atmospheric aerosols cause increased scattering of the beam radiation, which increases the proportion of diffuse radiation at the surface.

Eos, Transactions, American Geophysical Union↗

Field information links permafrost carbon to physical vulnerabilities of thawing

Deep soil profiles containing permafrost (Gelisols) were characterized for organic carbon (C) and total nitrogen (N) stocks to 3m depths. Using the Community Climate System Model (CCSM4) we calculate cumulative probability functions (PDFs) for active layer depths under current and future climates. The difference in PDFs over time was multiplied by C and N contents of soil horizons in Gelisol suborders to calculate newly thawed C and N, Thawing ranged from 147 PgC with 10 PgN by 2050 (representative concentration pathway RCP scenario 4.5) to 436 PgC with 29 PgN by 2100 (RCP 8.5). Organic horizons that thaw are vulnerable to combustion, and all horizon types are vulnerable to shifts in hydrology and decomposition. The rates and extent of such losses are unknown and can be further constrained by linking field and modelling approaches. These changes have the potential for strong additional loading to our atmosphere, water resources, and ecosystems.

Geophysical Research Letters↗

The influence of reservoirs, climate, land use and hydrologic conditions on loads and chemical quality of dissolved organic carbon in the Colorado River

Longitudinal patterns in dissolved organic carbon (DOC) loads and chemical quality were identified in the Colorado River from the headwaters in the Rocky Mountains to the United States-Mexico border from 1994 to 2011. Watershed- and reach-scale climate, land use, river discharge and hydrologic modification conditions that contribute to patterns in DOC were also identified. Principal components analysis (PCA) identified site-specific precipitation and reach-scale discharge as being correlated with sites in the upper basin, where there were increases in DOC load from the upstream to downstream direction. In the lower basin, where DOC load decreased from upstream to downstream, sites were correlated with site-specific temperature and reach-scale population, urban land use and hydrologic modification. In the reaches containing Lakes Powell and Mead, the two largest reservoirs in the United States, DOC quantity decreased, terrestrially derived aromatic DOC was degraded and/or autochthonous less aromatic DOC was produced. Taken together, these results suggest that longitudinal patterns in the relatively unregulated upper basin are influenced by watershed inputs of water and DOC, whereas DOC patterns in the lower basin are reflective of a balance between watershed contribution of water and DOC to the river and loss of water and DOC due to hydrologic modification and/or biogeochemical processes. These findings suggest that alteration of constituent fluxes in rivers that are highly regulated may overshadow watershed processes that would control fluxes in comparable unregulated rivers. Further, these results provide a foundation for detailed assessments of factors controlling the transport and chemical quality of DOC in the Colorado River.

Arizona, California, Colorado, Nevada, New Mexico,↗

Role of tidal wetland stability in lateral fluxes of particulate organic matter and carbon

Tidal wetland fluxes of particulate organic matter and carbon (POM, POC) are important terms in global budgets but remain poorly constrained. Given the link between sediment fluxes and wetland stability, POM and POC fluxes should also be related to stability. We measured POM and POC fluxes in eight microtidal salt marsh channels, with net POM fluxes ranging between −121 ± 33 (export) and 102 ± 28 (import) g OM·m −2 ·year −1 and net POC fluxes ranging between −52 ± 14 and 43 ± 12 g C·m −2 ·year −1 . A regression employing two measures of stability, the unvegetated‐vegetated marsh ratio (UVVR) and elevation, explained >95% of the variation in net fluxes. The regression indicates that marshes with lower elevation and UVVR import POM and POC while higher elevation marshes with high UVVR export POM and POC. We applied these relationships to marsh units within Barnegat Bay, New Jersey, USA, finding a net POM import of 2,355 ± 1,570 Mg OM/year (15 ± 10 g OM·m −2 ·year −1 ) and a net POC import of 1,263 ± 632 Mg C/year (8 ± 4 g C·m −2 ·year −1 ). The magnitude of this import was similar to an estimate of POM and POC export due to edge erosion (−2,535 Mg OM/year and − 1,291 Mg C/year), suggesting that this system may be neutral from a POM and POC perspective. In terms of a net budget, a disintegrating wetland should release organic material, while a stable wetland should trap material. This study quantifies that concept and demonstrates a linkage between POM/POC flux and geomorphic stability.

Limnology and Oceanography↗

Hydrologic export is a major component of coastal wetland carbon budgets

Coastal wetlands are among the most productive habitats on Earth and sequester globally significant amounts of atmospheric carbon (C). Extreme rates of soil C accumulation are widely assumed to reflect efficient C storage. Yet the fraction of wetland C lost via hydrologic export has not been directly quantified, since comprehensive budgets including direct estimates of lateral C loss are lacking. We present a complete net ecosystem C budget (NECB), demonstrating that lateral losses of C are a major component of the NECB for the largest stable brackish tidal marsh on the U.S. Pacific coast. Mean annual net ecosystem exchange of CO 2 with the atmosphere (NEE = −185 g C m 2 year −1 , negative NEE denoting ecosystem uptake) was compared to long-term soil C burial (87–110 g C m 2 year −1 ), suggesting only 47–59% of fixed atmospheric C accumulates in soils. Consistently, direct monitoring in 2017–2018 showed NEE of −255 g C m −2 year −1 , and hydrologic export of 105 g C m −2 year −1 (59% of NEE remaining on site). Despite their high C sequestration capacity, lateral losses from coastal wetlands are typically a larger fraction of the NECB when compared to other terrestrial ecosystems. Loss of inorganic C (the least measured NECB term) was 91% of hydrologic export and may be the most important term limiting C sequestration. The high productivity of coastal wetlands thus serves a dual function of C burial and estuarine export, and the multiple fates of fixed C must be considered when evaluating wetland capacity for C sequestration.

Global Biogeochemical Cycles↗

Carbon fluxes and microbial activities from boreal peatlands experiencing permafrost thaw

Permafrost thaw in northern ecosystems may cause large quantities of carbon (C) to move from soil to atmospheric pools. Because soil microbial communities play a critical role in regulating C fluxes from soils, we examined microbial activity and greenhouse gas production soon after permafrost thaw and ground collapse (into collapse-scar bogs), relative to the permafrost plateau or older thaw features. Using multiple field and laboratory-based assays at a field site in interior Alaska, we show that the youngest collapse-scar bog had the highest CH 4 production potential from soil incubations, and, based upon temporal changes in porewater concentrations and 13 C-CH 4 and 13 C-CO 2 , had greater summer in situ rates of respiration, methanogenesis, and surface CH 4 oxidation. These patterns could be explained by greater C and N availability in the young bog, while alternative terminal electron accepting processes did not play a significant role. Field diffusive CH 4 fluxes from the young bog were 4.1 times greater in the shoulder season and 1.7–7.2 times greater in winter relative to older bogs, but not during summer. Greater relative CH 4 flux rates in the shoulder season and winter could be due to reduced CH 4 oxidation relative to summer, magnifying the importance of differences in production. Both the permafrost plateau and collapse-scar bogs were sources of C to the atmosphere due in large part to winter C fluxes. In collapse scar bogs, winter is a critical period when differences in thermokarst age translates to differences in surface fluxes.

Alaska↗

Heterogeneous patterns of aged organic carbon export driven by hydrologic flow paths, soil texture, fire, and thaw in discontinuous permafrost headwaters

Climate change is thawing and potentially mobilizing vast quantities of organic carbon (OC) previously stored for millennia in permafrost soils of northern circumpolar landscapes. Climate-driven increases in fire and thermokarst may play a key role in OC mobilization by thawing permafrost and promoting transport of OC. Yet, the extent of OC mobilization and mechanisms controlling terrestrial-aquatic transfer are unclear. We demonstrate that hydrologic transport of soil dissolved OC (DOC) from the active layer and thawing permafrost to headwater streams is extremely heterogeneous and regulated by the interactions of soils, seasonal thaw, fire, and thermokarst. Repeated sampling of streams in eight headwater catchments of interior Alaska showed that the mean age of DOC for each stream ranges widely from modern to ∼2,000 years B.P. Together, an endmember mixing model and nonlinear, generalized additive models demonstrated that Δ 14 C-DOC signature (and mean age) increased from spring to fall, and was proportional to hydrologic contributions from a solute-rich water source, related to presumed deeper flow paths found predominantly in silty catchments. This relationship was correlated with and mediated by catchment properties. Mean DOC ages were older in catchments with >50% burned area, indicating that fire is also an important explanatory variable. These observations underscore the high heterogeneity in aged C export and difficulty of extrapolating estimates of permafrost-derived DOC export from watersheds to larger scales. Our results provide the foundation for developing a conceptual model of permafrost DOC export necessary for advancing understanding and prediction of land-water C exchange in changing boreal landscapes.

Alaska↗

Electrical properties of carbon dioxide hydrate: Implications for monitoring CO2 in the gas hydrate stability zone

CO 2 and CH 4 clathrate hydrates are of keen interest for energy and carbon cycle considerations. While both typically form on Earth as cubic structure I (sI), we find that pure CO 2 hydrate exhibits over an order of magnitude higher electrical conductivity ( σ ) than pure CH 4 hydrate at geologically relevant temperatures. The conductivity was obtained from frequency-dependent impedance ( Z ) measurements made on polycrystalline CO 2 hydrate (CO 2 ·6.0 ± 0.2H 2 O by methods here) with 25% gas-filled porosity, compared with CH 4 hydrate (CH 4 ·5.9H 2 O) formed and measured in the same apparatus and exhibiting closely matching grain characteristics. The conductivity of CO 2 hydrate is 6.5 × 10 −4 S/m at 273K with an activation energy ( E a ) of 46.5 kJ/mol at 260–281 K, compared with ∼5 × 10 −5 S/m and 34.8 kJ/m for CH 4 hydrate. Equivalent circuit modeling indicates that different pathways govern conduction in CO 2 versus CH 4 hydrate. Results show promise for use of electromagnetic methods in monitoring CO 2 hydrate formation in certain natural settings or in CO 2 /CH 4 exchange efforts.

Geophysical Research Letters↗

Influence of permafrost type and site history on losses of permafrost carbon after thaw

We quantified permafrost peat plateau and post-thaw carbon (C) stocks across a chronosequence in Interior Alaska to evaluate the amount of C lost with thaw. Macrofossil reconstructions revealed three stratigraphic layers of peat: (1) a base layer of fen/marsh peat, (2) peat from a forested peat plateau (with permafrost) and, (3) collapse-scar bog peat (at sites where permafrost thaw has occurred). Radiocarbon dating revealed that peat initiated within the last 2,500 years and that permafrost aggraded during the Little Ice Age (ca. 250 – 575 years ago) and degraded within the last several decades. The timing of permafrost thaw within each feature was not related to thaw bog size. Their rate of expansion may be more influenced by local factors, such as ground ice content and subsurface water inputs. We found C losses due to thaw over the past century were up to 46% of the C available, but the absolute amount of C lost (kg m -2 ) was over 50% lower than losses previously described in other Alaskan peatland chronosequences. We hypothesize that this difference stems from the process by which permafrost aggraded, with sites that formed permafrost epigenetically (significantly later than most peat accumulation) experiencing less absolute C loss with thaw than sites that formed syngenetically (simultaneously with peat accumulation). Epigenetic peat from our site had lower C:N ratios as compared to Alaskan sites that have syngenetic peat. This difference could help predict the magnitude of C loss with thaw across a range or permafrost types and histories.

Alaska↗

Climatic controls on soil carbon accumulation and loss in a dryland ecosystems

Arid and semiarid ecosystems drive year-to-year variability in the strength of the terrestrial carbon (C) sink, yet there is uncertainty about how soil C gains and losses contribute to this variation. To address this knowledge gap, we embedded C-depleted soil mesocosms, containing litter or biocrust C inputs, within an in situ dryland ecosystem warming experiment. Over the course of one year, changes in microbial biomass and total soil organic C pools were monitored alongside hourly measurements of soil CO 2 flux. We also developed a biogeochemical model to explore the mechanisms that gave rise to observed soil C dynamics. Field data and model simulations demonstrated that water exerted much stronger control on soil biogeochemistry than temperature, with precipitation events triggering large CO 2 pulses and transport of litter- and biocrust-derived C into the soil profile. We expected leaching of organic matter would result in steady accumulation of C within the mineral soil over time. Instead, the size of the total organic C pool fluctuated throughout the year, largely in response to microbial growth: increases in the size of microbial biomass were negatively correlated with the quantity of C residing in the top 2 cm, where most biogeochemical changes were observed. Our data and models suggest that microbial responses to precipitation events trigger rapid metabolism of dissolved organic C inputs, which strongly limit accumulation of autotroph-derived C belowground. Accordingly, changes in the magnitude and/or frequency of precipitation events in this dryland ecosystem could have profound impacts on the strength of the soil C sink.

Utah↗

Evaluating streamwater dissolved organic carbon dynamics in context of variable flowpath contributions with a tracer-based mixing model

This study focuses on characterizing the contributions of key terrestrial pathways that deliver dissolved organic carbon (DOC) to streams during hydrological events and on elucidating factors governing variation in water and DOC fluxes from these pathways. We made high-frequency measurements of discharge, specific conductance (SC), and fluorescent dissolved organic matter (FDOM) during 221 events recorded over 2 years within four Vermont (USA) watersheds that range in area from 0.4 to 139 km 2 . Using the SC measurements, together with statistical information on discharge, we separated the event hydrographs into contributions from three terrestrial pathways, which we refer to as riparian quickflow, subsurface quickflow, and slow-flow groundwater. The pathway discharges were used as input to a mixing model that closely approximated sub-hourly streamwater DOC concentrations as measured with the FDOM sensors. Subsurface quickflow, comprised of pre-event water, was the leading contributor to streamwater DOC fluxes, while riparian quickflow, comprised of event water, was the second-leading contributor to streamwater DOC fluxes, despite comprising the smallest proportion of streamflow yield among the three end-member pathways. Fixed-effects regression analysis revealed that the relationship between DOC fluxes from the end-member pathways and event magnitude was consistent across the four watersheds. This analysis also showed that DOC fluxes from the quickflow pathways increased significantly with temperature and varied inversely, but weakly, with catchment antecedent wetness. We believe that our approach, which leverages in-stream sensors that enable high-frequency measurements over extended periods, may be applicable for evaluating controls on DOC export from other watersheds within and beyond our study region.

New Hampshire, Vermont↗

A process-model perspective on recent changes in the carbon cycle of North America

Continental North America has been found to be a carbon (C) sink over recent decades by multiple studies employing a variety of estimation approaches. However, several key questions and uncertainties remain with these assessments. Here we used results from an ensemble of 19 state-of-the-art dynamic global vegetation models from the TRENDYv9 project to improve these estimates and study the drivers of its interannual variability. Our results show that North America has been a C sink with a magnitude of 0.37 ± 0.38 (mean and one standard deviation) PgC year −1 for the period 2000–2019 (0.31 and 0.44 PgC year −1 in each decade); split into 0.18 ± 0.12 PgC year −1 in Canada (0.15 and 0.20), 0.16 ± 0.17 in the United States (0.14 and 0.17), 0.02 ± 0.05 PgC year −1 in Mexico (0.02 and 0.02) and 0.01 ± 0.02 in Central America and the Caribbean (0.01 and 0.01). About 57% of the new C assimilated by terrestrial ecosystems is allocated into vegetation, 30% into soils, and 13% into litter. Losses of C due to fire account for 41% of the interannual variability of the mean net biome productivity for all North America in the model ensemble. Finally, we show that drought years (e.g., 2002) have the potential to shift the region to a small net C source in the simulations (−0.02 ± 0.46 PgC year −1 ). Our results highlight the importance of identifying the major drivers of the interannual variability of the continental-scale land C cycle along with the spatial distribution of local sink-source dynamics.

Journal of Geophysical Research Biogeosciences↗