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1.
  • Aldama-Campino, Aitor, et al. (författare)
  • Meridional Ocean Carbon Transport
  • 2020
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 34:9
  • Tidskriftsartikel (refereegranskat)abstract
    • The ocean's ability to take up and store CO2 is a key factor for understanding past and future climate variability. However, qualitative and quantitative understanding of surface‐to‐interior pathways, and how the ocean circulation affects the CO2 uptake, is limited. Consequently, how changes in ocean circulation may influence carbon uptake and storage and therefore the future climate remains ambiguous. Here we quantify the roles played by ocean circulation and various water masses in the meridional redistribution of carbon. We do so by calculating streamfunctions defined in dissolved inorganic carbon (DIC) and latitude coordinates, using output from a coupled biogeochemical‐physical model. By further separating DIC into components originating from the solubility pump and a residual including the biological pump, air‐sea disequilibrium, and anthropogenic CO2, we are able to distinguish the dominant pathways of how carbon enters particular water masses. With this new tool, we show that the largest meridional carbon transport occurs in a pole‐to‐equator transport in the subtropical gyres in the upper ocean. We are able to show that this pole‐to‐equator DIC transport and the Atlantic meridional overturning circulation (AMOC)‐related DIC transport are mainly driven by the solubility pump. By contrast, the DIC transport associated with deep circulation, including that in Antarctic bottom water and Pacific deep water, is mostly driven by the biological pump. As these two pumps, as well as ocean circulation, are widely expected to be impacted by anthropogenic changes, these findings have implications for the future role of the ocean as a climate‐buffering carbon reservoir.
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2.
  • Alfredsson, H., et al. (författare)
  • Estimated storage of amorphous silica in soils of the circum-Arctic tundra region
  • 2016
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 30:3, s. 479-500
  • Tidskriftsartikel (refereegranskat)abstract
    • We investigated the vertical distribution, storage, landscape partitioning, and spatial variability of soil amorphous silica (ASi) at four different sites underlain by continuous permafrost and representative of mountainous and lowland tundra, in the circum-Arctic region. Based on a larger set of data, we present the first estimate of the ASi soil reservoir (0-1 m depth) in circum-Arctic tundra terrain. At all sites, the vertical distribution of ASi concentrations followed the pattern of either (1) declining concentrations with depth (most common) or (2) increasing/maximum concentrations with depth. Our results suggest that a set of processes, including biological control, solifluction and other slope processes, cryoturbation, and formation of inorganic precipitates influence vertical distributions of ASi in permafrost terrain, with the capacity to retain stored ASi on millennial timescales. At the four study sites, areal ASi storage (0-1 m) is generally higher in graminoid tundra compared to wetlands. Our circum-Arctic upscaling estimates, based on both vegetation and soil classification separately, suggest a storage amounting to 219 ± 28 and 274 ± 33 Tmol Si, respectively, of which at least 30% is stored in permafrost. This estimate would account for about 3% of the global soil ASi storage while occupying an equal portion of the global land area. This result does not support the hypothesis that the circum-Arctic tundra soil ASi reservoir contains relatively higher amounts of ASi than other biomes globally as demonstrated for carbon. Nevertheless, climate warming has the potential to significantly alter ASi storage and terrestrial Si cycling in the Arctic.
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3.
  • Algesten, Grete, 1974-, et al. (författare)
  • Seasonal variation of CO2 saturation in the Gulf of Bothnia : Indications of marine net heterotrophy
  • 2004
  • Ingår i: Global Biogeochemical Cycles. - Washington, D.C : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 18, s. 4021-4028
  • Tidskriftsartikel (refereegranskat)abstract
    • Seasonal variation of pCO2 and primary and bacterioplankton production were measured in the Gulf of Bothnia during an annual cycle. Surface water was supersaturated with CO2 on an annual basis, indicating net heterotrophy and a source of CO2 to the atmosphere. However, the Gulf of Bothnia oscillated between being a sink and a source of CO2 over the studied period, largely decided by temporal variation in bacterial respiration (BR) and primary production (PP) in the water column above the pycnocline. The calculated annual respiration-production balance (BR-PP) was very similar to the estimated CO2 emission from the Gulf of Bothnia, which indicates that these processes were major determinants of the exchange of CO2 between water and atmosphere. The southern basin (the Bothnian Sea) had a lower net release of CO2 to the atmosphere than the northern Bothnian Bay (7.1 and 9.7 mmol C m−2 d−1, respectively), due to higher primary production, which to a larger extent balanced respiration in this basin.
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4.
  • Alling, Vanja, et al. (författare)
  • Non-conservative behavior of dissolved organic carbon across the Laptev and East Siberian Seas
  • 2010
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 24, s. GB4033-
  • Tidskriftsartikel (refereegranskat)abstract
    • Climate change is expected to have a strong effect on the Eastern Siberian Arctic Shelf (ESAS) region, which includes 40% of the Arctic shelves and comprises the Laptev and East Siberian seas. The largest organic carbon pool, the dissolved organic carbon (DOC), may change significantly due to changes in both riverine inputs and transformation rates; however, the present DOC inventories and transformation patterns are poorly understood. Using samples from the International Siberian Shelf Study 2008, this study examines for the first time DOC removal in Arctic shelf waters with residence times that range from months to years. Removals of up to 10%–20% were found in the Lena River estuary, consistent with earlier studies in this area, where surface waters were shown to have a residence time of approximately 2 months. In contrast, the DOC concentrations showed a strong nonconservative pattern in areas with freshwater residence times of several years. The average losses of DOC were estimated to be 30%–50% during mixing along the shelf, corresponding to a first-order removal rate constant of 0.3 yr−1. These data provide the first observational evidence for losses of DOC in the Arctic shelf seas, and the calculated DOC deficit reflects DOC losses that are higher than recent model estimates for the region. Overall, a large proportion of riverine DOC is removed from the surface waters across the Arctic shelves. Such significant losses must be included in models of the carbon cycle for the Arctic Ocean, especially since the breakdown of terrestrial DOC to CO2 in Arctic shelf seas may constitute a positive feedback mechanism for Arctic climate warming. These data also provide a baseline for considering the effects of future changes in carbon fluxes, as the vast northern carbon-rich permafrost areas draining into the Arctic are affected by global warming.
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5.
  • Ask, Jenny, et al. (författare)
  • Net ecosystem production in clear-water and brown-water lakes
  • 2012
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 26, s. GB1017-
  • Tidskriftsartikel (refereegranskat)abstract
    • We studied 15 lakes in northern Sweden with respect to primary production and respiration in benthic and pelagic habitats. The lakes were characterized by different concentrations of colored dissolved organic carbon (DOC) of terrestrial origin, forming a gradient ranging from clear-water to brown-water lakes. Primary production decreased and respiration increased on a whole-lake scale along the gradient of increasing DOC. Thus, the lakes became more net heterotrophic, i.e., had lower net ecosystem production (NEP = gross primary production - community respiration), with increasing terrestrial DOC and this change coincided with increasing partial pressure of carbon dioxide (pCO(2)) in the surface waters. The single most important process for the increasing net heterotrophy along the DOC gradient was pelagic respiration of terrestrial organic carbon. In spite of high metabolic activity in the benthic habitat, benthic primary production and benthic respiration decreased simultaneously with increasing DOC, showing that the benthic habitat was in metabolic balance throughout the gradient. Therefore, the net heterotrophic states of the lakes depended on the terrestrial DOC export to lakes and the concomitant respiration of terrestrial organic carbon in the pelagic habitat.
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6.
  • Banwart, Steven A., et al. (författare)
  • Process-based modeling of silicate mineral weathering responses to increasing atmospheric CO2 and climate change
  • 2009
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 23, s. GB4013-
  • Tidskriftsartikel (refereegranskat)abstract
    • A mathematical model describes silicate mineral weathering processes in modern soils located in the boreal coniferous region of northern Europe. The process model results demonstrate a stabilizing biological feedback mechanism between atmospheric CO2 levels and silicate weathering rates as is generally postulated for atmospheric evolution. The process model feedback response agrees within a factor of 2 of that calculated by a weathering feedback function of the type generally employed in global geochemical carbon cycle models of the Earth's Phanerozoic CO2 history. Sensitivity analysis of parameter values in the process model provides insight into the key mechanisms that influence the strength of the biological feedback to weathering. First, the process model accounts for the alkalinity released by weathering, whereby its acceleration stabilizes pH at values that are higher than expected. Although the process model yields faster weathering with increasing temperature, because of activation energy effects on mineral dissolution kinetics at warmer temperature, the mineral dissolution rate laws utilized in the process model also result in lower dissolution rates at higher pH values. Hence, as dissolution rates increase under warmer conditions, more alkalinity is released by the weathering reaction, helping maintain higher pH values thus stabilizing the weathering rate. Second, the process model yields a relatively low sensitivity of soil pH to increasing plant productivity. This is due to more rapid decomposition of dissolved organic carbon (DOC) under warmer conditions. Because DOC fluxes strongly influence the soil water proton balance and pH, this increased decomposition rate dampens the feedback between productivity and weathering. The process model is most sensitive to parameters reflecting soil structure; depth, porosity, and water content. This suggests that the role of biota to influence these characteristics of the weathering profile is as important, if not more important, than the role of biota to influence mineral dissolution rates through changes in soil water chemistry. This process-modeling approach to quantify the biological weathering feedback to atmospheric CO2 demonstrates the potential for a far more mechanistic description of weathering feedback in simulations of the global geochemical carbon cycle.
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7.
  • Bastviken, David, et al. (författare)
  • Methane emissions from lakes : Dependence of lake characteristics, two regional assessments, and a global estimate
  • 2004
  • Ingår i: Global Biogeochemical Cycles. - : Wiley-Blackwell Publishing Inc.. - 0886-6236 .- 1944-9224. ; 18, s. GB4009-
  • Tidskriftsartikel (refereegranskat)abstract
    • [ 1] Lake sediments are "hot spots'' of methane production in the landscape. However, regional and global lake methane emissions, contributing to the greenhouse effect, are poorly known. We developed predictions of methane emissions from easily measured lake characteristics based on measurements for 11 North American and 13 Swedish lakes, and literature values from 49 lakes. Results suggest that open water methane emission can be predicted from variables such as lake area, water depth, concentrations of total phosphorus, dissolved organic carbon, and methane, and the anoxic lake volume fraction. Using these relations, we provide regional estimates from lakes in Sweden and the upper midwest of the United States. Considering both open water and plant-mediated fluxes, we estimate global emissions as 8 - 48 Tg CH4 yr(-1) (6 - 16% of total natural methane emissions and greater than oceanic emission), indicating that lakes should be included as a significant source in global methane budgets.
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8.
  • Berggren, Martin, 1981-, et al. (författare)
  • Landscape regulation of bacterial growth efficiency in boreal freshwaters
  • 2007
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union. - 0886-6236 .- 1944-9224. ; 21
  • Tidskriftsartikel (refereegranskat)abstract
    • Allochthonous organic carbon in aquatic systems is metabolized by heterotrophic bacteria, with significant consequences for the biostructure and energy pathways of freshwater ecosystems. The degree to which allochthonous substrates support growth of bacteria is largely dependent on bacterial growth efficiency (BGE), i.e., bacterial production (BP) per unit of assimilated carbon. Here we show how the spatial variability of BGE in the boreal region can be mediated by the distribution of the two dominating landscape elements forest and mires. Using an 11 days bioassay approach, the production and respiration of bacteria were measured in water samples from nine small Swedish streams (64°N 19°E), representing a gradient ranging from organic carbon supplied mainly from peat mires to carbon supplied mainly from coniferous forests. BP was positively correlated to forest coverage (%) of the catchment, while bacterial respiration was similar in all streams. Consequently, BGE showed a strong positive correlation with forest coverage. Partial least square regression showed that BGE was chiefly regulated by qualitative properties of the organic material, indicated by the absorbance ratio a254/a365 plus C/N and C/P ratios. The data suggest that a share of the organic carbon pool, drained mainly from forest soils, had a potential of being incorporated into bacterial biomass with great efficiency. Its potential for supporting growth was probably nutrient regulated as indicated by inorganic nutrient enrichment experiments.
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9.
  • Björkman, Mats P., 1978, et al. (författare)
  • Winter carbon dioxide effluxes from Arctic ecosystems: An overview and comparison of methodologies
  • 2010
  • Ingår i: Global Biogeochemical Cycles. ; 24, s. GB3010-
  • Tidskriftsartikel (refereegranskat)abstract
    • The winter CO2 efflux from subnivean environments is an important component of annual C budgets in arctic ecosystems and consequently makes prediction and estimations of winter processes as well as incorporations of these processes into existing models important. Several methods have been used for estimating winter CO2 effluxes, involving different assumptions about the snow pack, all aiming to quantify CO2 production. Here, four different methods are compared and discussed: (1) measurements with a chamber on the snow surface, Fsnow; (2) chamber measurements directly on the soil, Fsoil, after snow removal; (3) diffusion measurements, F2-point, within the snow pack; and (4) a trace gas technique, FSF6, with multiple gas sampling within the snow pack. According to measurements collected from shallow and deep snow cover in High-Arctic Svalbard and Sub-Arctic Sweden during the winter of 2007-2008, the four methods differ by up to two orders of magnitude in their estimates of total winter emissions. The highest mean winter CO2 effluxes, 7.7-216.8 mg CO2 m-2 h-1, were observed using Fsoil and lowest values, 0.8-12.6 mg CO2 m-2 h-1, using FSF6. The Fsnow and F2-point methods were both within the lower range, 2.1-15.1 mg CO2 m-2 h-1 and 6.8-11.2 mg CO2 m-2 h-1, respectively. These differences are considered to be a result of contrasting methods, but also because the assumptions within the methods are not the same when quantifying CO2 production and effluxes to the atmosphere. Since snow can act as a barrier to CO2, Fsoil is assumed to measure soil production, whereas FSF6, Fsnow and F2-point are considered better approaches for quantifying exchange processes between the soil, snow, and the atmosphere. This study indicates that estimates of winter CO2 emissions may vary more as a result of the method used than due to the actual variation in soil CO2 production or release. This is a major concern, especially when CO2 efflux data are used in climate models or in carbon budget calculations, thus highlighting the need for further development and validation of accurate and appropriate techniques.
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10.
  • Björnerås, C., et al. (författare)
  • Widespread Increases in Iron Concentration in European and North American Freshwaters
  • 2017
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 31:10, s. 1488-1500
  • Tidskriftsartikel (refereegranskat)abstract
    • Recent reports of increasing iron (Fe) concentrations in freshwaters are of concern, given the fundamental role of Fe in biogeochemical processes. Still, little is known about the frequency and geographical distribution of Fe trends or about the underlying drivers. We analyzed temporal trends of Fe concentrations across 340 water bodies distributed over 10 countries in northern Europe and North America in order to gain a clearer understanding of where, to what extent, and why Fe concentrations are on the rise. We found that Fe concentrations have significantly increased in 28% of sites, and decreased in 4%, with most positive trends located in northern Europe. Regions with rising Fe concentrations tend to coincide with those with organic carbon (OC) increases. Fe and OC increases may not be directly mechanistically linked, but may nevertheless be responding to common regional-scale drivers such as declining sulfur deposition or hydrological changes. A role of hydrological factors was supported by covarying trends in Fe and dissolved silica, as these elements tend to stem from similar soil depths. A positive relationship between Fe increases and conifer cover suggests that changing land use and expanded forestry could have contributed to enhanced Fe export, although increases were also observed in nonforested areas. We conclude that the phenomenon of increasing Fe concentrations is widespread, especially in northern Europe, with potentially significant implications for wider ecosystem biogeochemistry, and for the current browning of freshwaters.
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11.
  • Bröder, Lisa, et al. (författare)
  • Quantifying Degradative Loss of Terrigenous Organic Carbon in Surface Sediments Across the Laptev and East Siberian Sea
  • 2019
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 33:1, s. 85-99
  • Tidskriftsartikel (refereegranskat)abstract
    • Ongoing permafrost thaw in the Arctic may remobilize large amounts of old organic matter. Upon transport to the Siberian shelf seas, this material may be degraded and released to the atmosphere, exported off-shelf, or buried in the sediments. While our understanding of the fate of permafrost-derived organic matter in shelf waters is improving, poor constraints remain regarding degradation in sediments. Here we use an extensive data set of organic carbon concentrations and isotopes (n=109) to inventory terrigenous organic carbon (terrOC) in surficial sediments of the Laptev and East Siberian Seas (LS + ESS). Of these similar to 2.7 Tg terrOC about 55% appear resistant to degradation on a millennial timescale. A first-order degradation rate constant of 1.5 kyr(-1) is derived by combining a previously established relationship between water depth and cross-shelf sediment-terrOC transport time with mineral-associated terrOC loadings. This yields a terrOC degradation flux of similar to 1.7Gg/year from surficial sediments during cross-shelf transport, which is orders of magnitude lower than earlier estimates for degradation fluxes of dissolved and particulate terrOC in the water column of the LS + ESS. The difference is mainly due to the low degradation rate constant of sedimentary terrOC, likely caused by a combination of factors: (i) the lower availability of oxygen in the sediments compared to fully oxygenated waters, (ii) the stabilizing role of terrOC-mineral associations, and (iii) the higher proportion of material that is intrinsically recalcitrant due to its chemical/molecular structure in sediments. Sequestration of permafrost-released terrOC in shelf sediments may thereby attenuate the otherwise expected permafrost carbon-climate feedback. Plain language summary Frozen soils in the Arctic contain large amounts of old organic matter. With ongoing climate change this previously freeze-locked carbon storage becomes vulnerable to transport and decay. Upon delivery to the shallow nearshore seas, it may either be directly degraded to carbon dioxide or methane and thereby fuel further warming or get buried and stored in sediments on the sea floor. Our understanding of the fate of carbon released from permafrost soils is increasing, yet uncertainties remain regarding its degradation in the sediment. Here we constrain how much land-derived organic carbon is deposited in the top layer of the sediment (the part that is prone to transport and exposed to oxygen-stimulated degradation) in the Laptev and East Siberian Seas. We find that more than half of this stock likely resists degradation, while the rest decays relatively slowly. Therefore, the amount of carbon released annually from degradation in surface sediments is much smaller than what was found to be emitted from overlying waters in earlier studies. We suspect that this difference is caused by a combination of mechanisms hindering degradation in sediments and thus conclude that the burial of land-derived carbon may help to dampen the climate impact of thawing permafrost.
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12.
  • Bubier, J.L., et al. (författare)
  • A comparison of methane flux in a boreal landscape between a dry and a wet year.
  • 2005
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 19:GB1023
  • Tidskriftsartikel (refereegranskat)abstract
    • We used field measurements of methane (CH4) flux from upland and wetland soils in the Northern Study Area (NSA) of BOREAS (BOReal Ecosystem-Atmosphere Study), near Thompson, Manitoba, during the summers of 1994 and 1996 to estimate the overall CH4 emission from a 1350 km2 landscape. June–September 1994 and 1996 were both drier and warmer than normal, but summer 1996 received 68 mm more precipitation than 1994, a 40% increase, and had a mean daily air temperature 0.6°C warmer than 1994. Upland soils consumed CH4 at rates from 0 to 1.0 mg m−2 d−1, with small spatial and temporal variations between years, and a weak dependence on soil temperature. In contrast, wetlands emitted CH4 at seasonal average rates ranging from 10 to 350 mg CH4 m−2 d−1, with high spatial and temporal variability, and increased an average of 60% during the wetter and warmer 1996. We used Landsat imagery, supervised classification, and ground truthing to scale point CH4 fluxes (<1 m2) to the landscape (>1000 km2). We performed a sensitivity analysis for error terms in both areal coverage and CH4 flux, showing that the small areas of high CH4 emission (e.g., small ponds, graminoid fens, and permafrost collapse margins) contribute the largest uncertainty in both flux measurements and mapping. Although wetlands cover less than 30% of the landscape, areally extrapolated CH4 flux for the NSA increased by 61% from 10 to16 mg CH4 m−2 d−1 between years, entirely attributed to the increase in wetland CH4 emission. We conclude that CH4 fluxes will tend to be underestimated in areas where much of the landscape is covered by wetlands. This is due to the large spatial and temporal variability encountered in chamber-based measurements of wetland CH4 fluxes, strong sensitivity of wetland CH4 emission to small changes in climate, and because most remote sensing images do not adequately identify small areas of high CH4 flux.
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13.
  • Burdett, Heidi L., et al. (författare)
  • Coralline algae as a globally significant pool of marine dimethylated sulfur
  • 2015
  • Ingår i: Global Biogeochemical Cycles. - : Blackwell Publishing. - 0886-6236 .- 1944-9224. ; 29:10, s. 1845-1853
  • Tidskriftsartikel (refereegranskat)abstract
    • Marine algae are key sources of the biogenic sulfur compound dimethylsulphoniopropionate (DMSP), a vital component of the marine sulfur cycle. Autotrophic ecosystem engineers such as red coralline algae support highly diverse and biogeochemically active ecosystems and are known to be high DMSP producers, but their importance in the global marine sulfur cycle has not yet been appreciated. Using a global sampling approach, we show that red coralline algae are a globally significant pool of DMSP in the oceans, estimated to be similar to 110x10(12) moles worldwide during the summer months. Latitude was a major driver of observed regional-scale variations, with peaks in polar and tropical climate regimes, reflecting the varied cellular functions for DMSP (e.g., as a cryoprotectant and antioxidant). A temperate coralline algal bed was investigated in more detail to also identify local-scale temporal variations. Here, water column DMSP was driven by water temperature, and to a lesser extent, cloud cover; two factors which are also vital in controlling coralline algal growth. This study demonstrates that coralline algae harbor a large pool of dimethylated sulfur, thereby playing a significant role in both the sulfur and carbon marine biogeochemical cycles. However, coralline algal habitats are severely threatened by projected climate change; a loss of this habitat may thus detrimentally impact oceanic sulfur and carbon biogeochemical cycling.
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14.
  • Campeau, Audrey, et al. (författare)
  • Controls on the 14C Content of Dissolved and Particulate Organic Carbon Mobilized Across the Mackenzie River Basin, Canada
  • 2020
  • Ingår i: Global Biogeochemical Cycles. - : AMER GEOPHYSICAL UNION. - 0886-6236 .- 1944-9224. ; 34:12
  • Tidskriftsartikel (refereegranskat)abstract
    • The Mackenzie River Basin (MRB) delivers large quantities of organic carbon (OC) into the Arctic Ocean, with significant implications for the global C budgets and ocean biogeochemistry. The amount and properties of OC in the Mackenzie River's delta have been well monitored in the last decade, but the spatial variability in OC sources transported by its different tributaries is still unclear. Here we present new data on the radiocarbon (14C) content of dissolved and particulate OC (Δ14C‐DOC and Δ14C‐POC) across the mainstem and major tributaries of the MRB, comprising 19 different locations, to identify factors controlling spatial patterns in riverine OC sources. The Δ14C‐DOC and Δ14C‐POC varied across a large range, from −179.9‰ to 62.9‰, and −728.8‰ to −9.0‰, respectively. Our data reveal a positive spatial coupling between the Δ14C of DOC and POC across the MRB, whereby the most 14C‐depleted waters were issued from the mountainous west bank of the MRB. This 14C‐depleted DOC and POC likely originates from a combination of petrogenic sources, connected with the presence of kerogens in the bedrock, and biogenic sources, mobilized by thawing permafrost. Our analysis also reveals intriguing relationships between Δ14C of DOC and POC with turbidity, water stable isotope ratio and catchment elevation, indicating that hydrology and geomorphology are key to understanding riverine OC sources in this landscape. A closer examination of the specific mechanisms giving rise to these relationships is recommended. For now, this study provides a road map of the key OC sources in this rapidly changing river basin.
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15.
  • Campeau, Audrey, et al. (författare)
  • Regional contribution of CO2 and CH4 fluxes from the fluvial network in a lowland boreal landscape of Quebec
  • 2014
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 28:1, s. 57-69
  • Tidskriftsartikel (refereegranskat)abstract
    • Boreal rivers and streams are known as hot spots of CO2 emissions, yet their contribution to CH4 emissions has traditionally been assumed to be negligible, due to the spatially fragmented data and lack of regional studies addressing both gases simultaneously. Here we explore the regional patterns in river CO2 and CH4 concentrations (pCO(2) and pCH(4)), gas exchange coefficient (k), and the resulting emissions in a lowland boreal region of Northern Quebec. Rivers and streams were systematically supersaturated in both gases, with both pCO(2) and pCH(4) declining along the river continuum. The k was on average low and increased with stream order, consistent with the hydrology of this flat landscape. The smallest streams (order 1), which represent <20% of the total river surface, contributed over 35% of the total fluvial greenhouse gas (GHG) emissions. The end of winter and the spring thaw periods, which are rarely included in annual emission budgets, contributed on average 21% of the annual GHG emissions. As a whole, the fluvial network acted as significant source of both CO2 and CH4, releasing on average 1.5 tons of C (CO2 eq) yr(-1)km(-2) of landscape, of which CH4 emissions contributed approximately 34%. We estimate that fluvial CH4 emissions represent 41% of the regional aquatic (lakes, reservoirs, and rivers) CH4 emissions, despite the relatively small riverine surface (4.3% of the total aquatic surface). We conclude that these fluvial networks in boreal lowlands play a disproportionately large role as hot spots for CO2 and more unexpectedly for CH4 emissions. Key Points pCO(2) and pCH(4) decrease, whereas the k600 increases with increasing stream order Small streams and spring thaw period play a large role in regional C balance Rivers are significant sources of CO2 and unexpectedly large sources of CH4
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16.
  • Carstensen, Jacob, et al. (författare)
  • Long-Term and Seasonal Trends in Estuarine and Coastal Carbonate Systems
  • 2018
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 32:3, s. 497-513
  • Tidskriftsartikel (refereegranskat)abstract
    • Coastal pH and total alkalinity are regulated by a diverse range of local processes superimposed on global trends of warming and ocean acidification, yet few studies have investigated the relative importance of different processes for coastal acidification. We describe long-term (1972-2016) and seasonal trends in the carbonate system of three Danish coastal systems demonstrating that hydrological modification, changes in nutrient inputs from land, and presence/absence of calcifiers can drastically alter carbonate chemistry. Total alkalinity was mainly governed by conservative mixing of freshwater (0.73-5.17mmolkg(-1)) with outer boundary concentrations (similar to 2-2.4mmolkg(-1)), modulated seasonally and spatially (similar to 0.1-0.2mmolkg(-1)) by calcifiers. Nitrate assimilation by primary production, denitrification, and sulfate reduction increased total alkalinity by almost 0.6mmolkg(-1) in the most eutrophic system during a period without calcifiers. Trends in pH ranged from -0.0088year(-1) to 0.021year(-1), the more extreme of these mainly driven by salinity changes in a sluice-controlled lagoon. Temperature increased 0.05 degrees Cyr(-1) across all three systems, which directly accounted for a pH decrease of 0.0008year(-1). Accounting for mixing, salinity, and temperature effects on dissociation and solubility constants, the resulting pH decline (0.0040year(-1)) was about twice the ocean trend, emphasizing the effect of nutrient management on primary production and coastal acidification. Coastal pCO(2) increased similar to 4 times more rapidly than ocean rates, enhancing CO2 emissions to the atmosphere. Indeed, coastal systems undergo more drastic changes than the ocean and coastal acidification trends are substantially enhanced from nutrient reductions to address coastal eutrophication.
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17.
  • Catalán, Núria, 1985-, et al. (författare)
  • Behind the Scenes : mechanisms Regulating Climatic Patterns of Dissolved Organic Carbon Uptake in Headwater Streams
  • 2018
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 32:10, s. 1528-1541
  • Tidskriftsartikel (refereegranskat)abstract
    • Large variability in dissolved organic carbon (DOC) uptake rates has been reported for headwater streams, but the causes of this variability are still not well understood. Here we assessed acetate uptake rates across 11 European streams comprising different ecoregions by using whole-reach pulse acetate additions. We evaluated the main climatic and biogeochemical drivers of acetate uptake during two seasonal periods. Our results show a minor influence of sampling periods but a strong effect of climate and dissolved organic matter (DOM) composition on acetate uptake. In particular, mean annual precipitation explained half of the variability of the acetate uptake velocities (Vf(Acetate)) across streams. Temperate streams presented the lowest Vf(Acetate), together with humic-like DOM and the highest stream respiration rates. In contrast, higher Vf(Acetate) were found in semiarid streams, with protein-like DOM, indicating a dominance of reactive, labile compounds. This, together with lower stream respiration rates and molar ratios of DOC to nitrate, suggests a strong C limitation in semiarid streams, likely due to reduced inputs from the catchment. Overall, this study highlights the interplay of climate and DOM composition and its relevance to understand the biogeochemical mechanisms controlling DOC uptake in streams. Plain Language Summary Headwater streams receive and degrade organic carbon and nutrients from the surrounding catchments. That degradation can be assessed by measuring the uptake of simple compounds of carbon or nitrogen such as acetate or nitrate. Here we determine the variability in acetate and nitrate uptake rates across headwater streams and elucidate the mechanisms behind that variability. The balance between nutrients, the composition of the organic materials present in the streams, and the climatic background is at interplay.
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18.
  • Chadburn, Sarah E., et al. (författare)
  • Modeled Microbial Dynamics Explain the Apparent Temperature Sensitivity of Wetland Methane Emissions
  • 2020
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 34:11
  • Tidskriftsartikel (refereegranskat)abstract
    • Methane emissions from natural wetlands tend to increase with temperature and therefore may lead to a positive feedback under future climate change. However, their temperature response includes confounding factors and appears to differ on different time scales. Observed methane emissions depend strongly on temperature on a seasonal basis, but if the annual mean emissions are compared between sites, there is only a small temperature effect. We hypothesize that microbial dynamics are a major driver of the seasonal cycle and that they can explain this apparent discrepancy. We introduce a relatively simple model of methanogenic growth and dormancy into a wetland methane scheme that is used in an Earth system model. We show that this addition is sufficient to reproduce the observed seasonal dynamics of methane emissions in fully saturated wetland sites, at the same time as reproducing the annual mean emissions. We find that a more complex scheme used in recent Earth system models does not add predictive power. The sites used span a range of climatic conditions, with the majority in high latitudes. The difference in apparent temperature sensitivity seasonally versus spatially cannot be recreated by the non-microbial schemes tested. We therefore conclude that microbial dynamics are a strong candidate to be driving the seasonal cycle of wetland methane emissions. We quantify longer-term temperature sensitivity using this scheme and show that it gives approximately a 12% increase in emissions per degree of warming globally. This is in addition to any hydrological changes, which could also impact future methane emissions.
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19.
  • Choi, J. H., et al. (författare)
  • Influence of Biogenic Organics on the Chemical Composition of Arctic Aerosols
  • 2019
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 33:10, s. 1238-1250
  • Tidskriftsartikel (refereegranskat)abstract
    • We use an ultrahigh-resolution 15-T Fourier transform ion cyclotron resonance mass spectrometer to elucidate the compositional changes in Arctic organic aerosols collected at Ny-angstrom lesund, Svalbard, in May 2015. The Fourier transform ion cyclotron resonance mass spectrometer analysis of airborne organic matter provided information on the molecular compositions of aerosol particles collected during the Arctic spring period. The air mass transport history, combined with satellite-derived geographical information and chlorophyll concentration data, revealed that the molecular compositions of organic aerosols drastically differed depending on the origin of the potential source region. The protein and lignin compound populations contributed more than 70% of the total intensity of assigned molecules when the air masses mainly passed over the ocean region. Interestingly, the intensity of microbe-derived organics (protein and carbohydrate compounds) was positively correlated with the air mass exposure to phytoplankton biomass proxied as chlorophyll. Furthermore, the intensities of lignin and unsaturated hydrocarbon compounds, typically derived from terrestrial vegetation, increased with an increase in the advection time of the air mass over the ocean domain. These results suggest that the accumulation of dissolved biogenic organics in the Arctic Ocean possibly derived from both phytoplankton and terrestrial vegetation could significantly influence the chemical properties of Arctic organic aerosols during a productive spring period. The interpretation of molecular changes in organic aerosols using an ultrahigh-resolution mass spectrometer could provide deep insight for understanding organic aerosols in the atmosphere over the Arctic and the relationship of organic aerosols with biogeochemical processes in terms of aerosol formation and environmental changes.
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20.
  • Costello, David M., et al. (författare)
  • Global patterns and controls of nutrient immobilization on decomposing cellulose in riverine ecosystems
  • 2022
  • Ingår i: Global Biogeochemical Cycles. - : John Wiley & Sons. - 0886-6236 .- 1944-9224. ; 36:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Microbes play a critical role in plant litter decomposition and influence the fate of carbon in rivers and riparian zones. When decomposing low-nutrient plant litter, microbes acquire nitrogen (N) and phosphorus (P) from the environment (i.e., nutrient immobilization), and this process is potentially sensitive to nutrient loading and changing climate. Nonetheless, environmental controls on immobilization are poorly understood because rates are also influenced by plant litter chemistry, which is coupled to the same environmental factors. Here we used a standardized, low-nutrient organic matter substrate (cotton strips) to quantify nutrient immobilization at 100 paired stream and riparian sites representing 11 biomes worldwide. Immobilization rates varied by three orders of magnitude, were greater in rivers than riparian zones, and were strongly correlated to decomposition rates. In rivers, P immobilization rates were controlled by surface water phosphate concentrations, but N immobilization rates were not related to inorganic N. The N:P of immobilized nutrients was tightly constrained to a molar ratio of 10:1 despite wide variation in surface water N:P. Immobilization rates were temperature-dependent in riparian zones but not related to temperature in rivers. However, in rivers nutrient supply ultimately controlled whether microbes could achieve the maximum expected decomposition rate at a given temperature. Collectively, we demonstrated that exogenous nutrient supply and immobilization are critical control points for decomposition of organic matter.
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21.
  • Dahl, Martin, 1984-, et al. (författare)
  • A 2,000-Year Record of Eelgrass (Zostera marina L.) : Colonization Shows Substantial Gains in Blue Carbon Storage and Nutrient Retention
  • 2024
  • Ingår i: Global Biogeochemical Cycles. - : John Wiley & Sons. - 0886-6236 .- 1944-9224. ; 38:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Assessing historical environmental conditions linked to habitat colonization is important for understanding long-term resilience and improving conservation and restoration efforts. Such information is lacking for the seagrass Zostera marina, an important foundation species across cold-temperate coastal areas of the Northern Hemisphere. Here, we reconstructed environmental conditions during the last 14,000 years from sediment cores in two eelgrass (Z. marina) meadows along the Swedish west coast, with the main aims to identify the time frame of seagrass colonization and describe subsequent biogeochemical changes following establishment. Based on vegetation proxies (lipid biomarkers), eelgrass colonization occurred about 2,000 years ago after geomorphological changes that resulted in a shallow, sheltered environment favoring seagrass growth. Seagrass establishment led to up to 20- and 24-fold increases in sedimentary carbon and nitrogen accumulation rates, respectively. This demonstrates the capacity of seagrasses as efficient ecosystem engineers and their role in global change mitigation and adaptation through CO2 removal, and nutrient and sediment retention. By combining regional climate projections and landscape models, we assessed potential climate change effects on seagrass growth, productivity and distribution until 2100. These predictions showed that seagrass meadows are mostly at risk from increased sedimentation and hydrodynamic changes, while the impact from sea level rise alone might be of less importance in the studied area. This study showcases the positive feedback between seagrass colonization and environmental conditions, which holds promise for successful conservation and restoration efforts aimed at supporting climate change mitigation and adaptation, and the provision of several other crucial ecosystem services. © 2024. The Authors.
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22.
  • Daniau, A. -L, et al. (författare)
  • predictability of biomass burning in response to climate changes
  • 2012
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 26, s. GB4007-
  • Tidskriftsartikel (refereegranskat)abstract
    • Climate is an important control on biomass burning, but the sensitivity of fire to changes in temperature and moisture balance has not been quantified. We analyze sedimentary charcoal records to show that the changes in fire regime over the past 21,000 yrs are predictable from changes in regional climates. Analyses of paleo-fire data show that fire increases monotonically with changes in temperature and peaks at intermediate moisture levels, and that temperature is quantitatively the most important driver of changes in biomass burning over the past 21,000 yrs. Given that a similar relationship between climate drivers and fire emerges from analyses of the interannual variability in biomass burning shown by remote-sensing observations of month-by-month burnt area between 1996 and 2008, our results signal a serious cause for concern in the face of continuing global warming.
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23.
  • Darracq, A., et al. (författare)
  • Long-term development of Phosphorus and Nitrogen loads through the subsurface and surface water systems of drainage basins
  • 2008
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 22:3, s. GB3022-
  • Tidskriftsartikel (refereegranskat)abstract
    • We analyze and compare simulations and controlling processes of the past 60 years and possible future short-and long-term development of phosphorus and nitrogen loading from the Swedish Norrstrom drainage basin to the Baltic Sea under different inland source management scenarios. Results indicate that both point and agricultural source inputs may need to be decreased by at least 40% in order to reach a long-term sustainable 30% reduction of anthropogenic coastal nitrogen loading, as required by national environmental goals. A corresponding 20% anthropogenic phosphorus load reduction goal may be reached in the short term by analogous combined 40% source input reduction, but appears impossible to maintain as a long-term achievement by inland source abatement only. In general, realistic quantification of the slow subsurface nutrient transport and accumulation-release dynamics may be essential for accurately predicting and managing nutrient loading to surface and coastal waters.
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24.
  • Eckdahl, Johan A., et al. (författare)
  • Mineral soils are an important intermediate storage pool of black carbon in fennoscandian boreal forests
  • 2022
  • Ingår i: Global Biogeochemical Cycles. - : John Wiley & Sons. - 0886-6236 .- 1944-9224. ; 36:11
  • Tidskriftsartikel (refereegranskat)abstract
    • Approximately 40% of earth's carbon (C) stored in land vegetation and soil is within the boreal region. This large C pool is subjected to substantial removals and transformations during periodic wildfire. Fire-altered C, commonly known as pyrogenic carbon (PyC), plays a significant role in forest ecosystem functioning and composes a considerable fraction of C transport to limnic and oceanic sediments. While PyC stores are beginning to be quantified globally, knowledge is lacking regarding the drivers of their production and transport across ecosystems. This study used the chemo-thermal oxidation at 375°C (CTO-375) method to isolate a particularly refractory subset of PyC compounds, here called black carbon (BC), finding an average increase of 11.6 g BC m−2 at 1 year postfire in 50 separate wildfires occurring in Sweden during 2018. These increases could not be linked to proposed drivers, however BC storage in 50 additional nearby unburnt soils related strongly to soil mass while its proportion of the larger C pool related negatively to soil C:N. Fire approximately doubled BC stocks in the mineral layer but had no significant effect on BC in the organic layer where it was likely produced. Suppressed decomposition rates and low heating during fire in mineral subsoil relative to upper layers suggests potential removals of the doubled mineral layer BC are more likely transported out of the soil system than degraded in situ. Therefore, mineral soils are suggested to be an important storage pool for BC that can buffer short-term (production in fire) and long-term (cross-ecosystem transport) BC cycling.
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25.
  • Fatichi, Simone, et al. (författare)
  • A Mechanistic Model of Microbially Mediated Soil Biogeochemical Processes : A Reality Check
  • 2019
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 33:6, s. 620-648
  • Tidskriftsartikel (refereegranskat)abstract
    • Present gaps in the representation of key soil biogeochemical processes such as the partitioning of soil organic carbon among functional components, microbial biomass and diversity, and the coupling of carbon and nutrient cycles present a challenge to improving the reliability of projected soil carbon dynamics. We introduce a new soil biogeochemistry module linked with a well-tested terrestrial biosphere model T&C. The module explicitly distinguishes functional soil organic carbon components. Extracellular enzymes and microbial pools are differentiated based on the functional roles of bacteria, saprotrophic, and mycorrhizal fungi. Soil macrofauna is also represented. The model resolves the cycles of nitrogen, phosphorus, and potassium. Model simulations for 20 sites compared favorably with global patterns of litter and soil stoichiometry, microbial and macrofaunal biomass relations with soil organic carbon, soil respiration, and nutrient mineralization rates. Long-term responses to bare fallow and nitrogen addition experiments were also in agreement with observations. Some discrepancies between predictions and observations are appreciable in the response to litter manipulation. Upon successful model reproduction of observed general trends, we assessed patterns associated with the carbon cycle that were challenging to address empirically. Despite large site-to-site variability, fine root, fungal, bacteria, and macrofaunal respiration account for 33%, 40%, 24%, and 3% on average of total belowground respiration, respectively. Simulated root exudation and carbon export to mycorrhizal fungi represent on average about 13% of plant net primary productivity. These results offer mechanistic and general estimates of microbial biomass and its contribution to respiration fluxes and to soil organic matter dynamics.
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26.
  • Feng, Xiaojuan, et al. (författare)
  • Multimolecular tracers of terrestrial carbon transfer across the pan-Arctic : C-14 characteristics of sedimentary carbon components and their environmental controls
  • 2015
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 29:11, s. 1855-1873
  • Tidskriftsartikel (refereegranskat)abstract
    • Distinguishing the sources, ages, and fate of various terrestrial organic carbon (OC) pools mobilized from heterogeneous Arctic landscapes is key to assessing climatic impacts on the fluvial release of carbon from permafrost. Through molecular C-14 measurements, including novel analyses of suberin- and/or cutin-derived diacids (DAs) and hydroxy fatty acids (FAs), we compared the radiocarbon characteristics of a comprehensive suite of terrestrial markers (including plant wax lipids, cutin, suberin, lignin, and hydroxy phenols) in the sedimentary particles from nine major arctic and subarctic rivers in order to establish a benchmark assessment of the mobilization patterns of terrestrial OC pools across the pan-Arctic. Terrestrial lipids, including suberin-derived longer-chain DAs (C-24,C-26,C-28), plant wax FAs (C(24,26,2)8), and n-alkanes (C-27,C-29,C-31), incorporated significant inputs of aged carbon, presumably from deeper soil horizons. Mobilization and translocation of these old terrestrial carbon components was dependent on nonlinear processes associated with permafrost distributions. By contrast, shorter-chain (C-16,C-18) DAs and lignin phenols (as well as hydroxy phenols in rivers outside eastern Eurasian Arctic) were much more enriched in C-14, suggesting incorporation of relatively young carbon supplied by runoff processes from recent vegetation debris and surface layers. Furthermore, the radiocarbon content of terrestrial markers is heavily influenced by specific OC sources and degradation status. Overall, multitracer molecular C-14 analysis sheds new light on the mobilization of terrestrial OC from arctic watersheds. Our findings of distinct ages for various terrestrial carbon components may aid in elucidating fate of different terrestrial OC pools in the face of increasing arctic permafrost thaw.
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27.
  • Fetzel, T., et al. (författare)
  • Quantification of uncertainties in global grazing systems assessment
  • 2017
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 31:7, s. 1089-1102
  • Tidskriftsartikel (refereegranskat)abstract
    • Livestock systems play a key role in global sustainability challenges like food security and climate change, yet many unknowns and large uncertainties prevail. We present a systematic, spatially explicit assessment of uncertainties related to grazing intensity (GI), a key metric for assessing ecological impacts of grazing, by combining existing data sets on (a) grazing feed intake, (b) the spatial distribution of livestock, (c) the extent of grazing land, and (d) its net primary productivity (NPP). An analysis of the resulting 96 maps implies that on average 15% of the grazing land NPP is consumed by livestock. GI is low in most of the world's grazing lands, but hotspots of very high GI prevail in 1% of the total grazing area. The agreement between GI maps is good on one fifth of the world's grazing area, while on the remainder, it is low to very low. Largest uncertainties are found in global drylands and where grazing land bears trees (e.g., the Amazon basin or the Taiga belt). In some regions like India or Western Europe, massive uncertainties even result in GI > 100% estimates. Our sensitivity analysis indicates that the input data for NPP, animal distribution, and grazing area contribute about equally to the total variability in GI maps, while grazing feed intake is a less critical variable. We argue that a general improvement in quality of the available global level data sets is a precondition for improving the understanding of the role of livestock systems in the context of global environmental change or food security. Plain Language Summary Livestock systems play a key role in global sustainability challenges like food security and climate change, yet many unknowns and large uncertainties prevail. We present a systematic assessment of uncertainties related to the intensity of grazing, a key metric for assessing ecological impacts of grazing. We combine existing data sets on (a) grazing feed intake, (b) the spatial distribution of livestock, (c) the extent of grazing land, and (d) the biomass available for grazing. Our results show that most grasslands are used with low intensity, but hotspots of high intensity prevail on 1% of the global grazing area, mainly located in drylands and where grazing land bears trees. The agreement between all maps is good on one fifth of the global grazing area, while on the remainder, it is low to very low. Our sensitivity analysis indicates that the input data for available biomass, animal distribution, and grazing area contribute about equally to the total variability of our maps, while grazing feed intake is a less critical variable. We argue that a general improvement in quality of the available data sets is a precondition for improving the understanding of livestock systems in the context of global environmental change or food security.
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28.
  • Fisher, Rebecca E., et al. (författare)
  • Measurement of the C-13 isotopic signature of methane emissions from northern European wetlands
  • 2017
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 31:3, s. 605-623
  • Tidskriftsartikel (refereegranskat)abstract
    • Isotopic data provide powerful constraints on regional and global methane emissions and their source profiles. However, inverse modeling of spatially resolved methane flux is currently constrained by a lack of information on the variability of source isotopic signatures. In this study, isotopic signatures of emissions in the Fennoscandian Arctic have been determined in chambers over wetland, in the air 0.3 to 3m above the wetland surface and by aircraft sampling from 100m above wetlands up to the stratosphere. Overall, the methane flux to atmosphere has a coherent delta C-13 isotopic signature of -71 +/- 1%, measured in situ on the ground in wetlands. This is in close agreement with delta C-13 isotopic signatures of local and regional methane increments measured by aircraft campaigns flying through air masses containing elevated methane mole fractions. In contrast, results from wetlands in Canadian boreal forest farther south gave isotopic signatures of -67 +/- 1%. Wetland emissions dominate the local methane source measured over the European Arctic in summer. Chamber measurements demonstrate a highly variable methane flux and isotopic signature, but the results from air sampling within wetland areas show that emissions mix rapidly immediately above the wetland surface and methane emissions reaching the wider atmosphere do indeed have strongly coherent C isotope signatures. The study suggests that for boreal wetlands (>60 degrees N) global and regional modeling can use an isotopic signature of -71 parts per thousand to apportion sources more accurately, but there is much need for further measurements over other wetlands regions to verify this.
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29.
  • Fransner, Filippa, et al. (författare)
  • Tracing terrestrial DOC in the Baltic Sea - a 3-D model study
  • 2016
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 30:2, s. 134-148
  • Tidskriftsartikel (refereegranskat)abstract
    • The fate of terrestrial organic matter brought to the coastal seas by rivers, and its role in the global carbon cycle, are still not very well known. Here the degradation rate of terrestrial dissolved organic carbon (DOCter) is studied in the Baltic Sea, a subarctic semi-enclosed sea, by releasing it as a tracer in a 3-D circulation model and applying linear decay constants. A good agreement with available observational data is obtained by parameterizing the degradation in two rather different ways; one by applying a decay time on the order of 10 years to the whole pool of DOCter, and one by dividing the DOCter into one refractory pool and one pool subject to a decay time on the order of 1 year. The choice of parameterization has a significant effect on where in the Baltic Sea the removal takes place, which can be of importance when modeling the full carbon cycle and the CO2 exchange with the atmosphere. In both cases the biogeochemical decay operates on time scales less than the water residence time. Therefore only a minor fraction of the DOCter reaches the North Sea, whereas approximately 80% is removed by internal sinks within the Baltic Sea. This further implies that DOCter mineralization is an important link in land-sea-atmosphere cycling of carbon in coastal- and shelf seas that are heavily influenced by riverine DOC.
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30.
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31.
  • Giesler, Reiner, et al. (författare)
  • Spatiotemporal variations of pCO(2) and delta C-13-DIC in subarctic streams in northern Sweden
  • 2013
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 27:1, s. 176-186
  • Tidskriftsartikel (refereegranskat)abstract
    • Current predictions of climate-related changes in high-latitude environments suggest major effects on the C export in streams and rivers. To what extent this will also affect the stream water CO2 concentrations is poorly understood. In this study we examined the spatiotemporal variation in partial pressure of CO2 (pCO(2)) and in stable isotopic composition of dissolved inorganic carbon (delta C-13-DIC) in subarctic streams in northern Sweden. The selected watersheds are characterized by large variations in high-latitude boreal forest and tundra and differences in bedrock. We found that all streams generally were supersaturated in pCO(2) with an average concentration of 850 mu atm. The variability in pCO(2) across streams was poorly related to vegetation cover, and carbonaceous bedrock influence was manifested in high DIC concentrations but not reflected in either stream pCO(2) or delta C-13-DIC. Stream water pCO(2) values were highest during winter base flow when we also observed the lowest delta C-13-DIC values, and this pattern is interpreted as a high contribution from CO2 from soil respiration. Summer base flow delta C-13-DIC values probably are more affected by in situ stream processes such as aquatic production/respiration and degassing. A challenge for further studies will be to disentangle the origin of stream water CO2 and quantify their relative importance.
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32.
  • Gottselig, N., et al. (författare)
  • Elemental Composition of Natural Nanoparticles and Fine Colloids in European Forest Stream Waters and Their Role as Phosphorus Carriers
  • 2017
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 31:10, s. 1592-1607
  • Tidskriftsartikel (refereegranskat)abstract
    • Biogeochemical cycling of elements largely occurs in dissolved state, but many elements may also be bound to natural nanoparticles (NNP, 1-100 nm) and fine colloids (100-450 nm). We examined the hypothesis that the size and composition of stream water NNP and colloids vary systematically across Europe. To test this hypothesis, 96 stream water samples were simultaneously collected in 26 forested headwater catchments along two transects across Europe. Three size fractions (~1-20 nm, >20-60 nm, and >60 nm) of NNP and fine colloids were identified with Field Flow Fractionation coupled to inductively coupled plasma mass spectrometry and an organic carbon detector. The results showed that NNP and fine colloids constituted between 2 ± 5% (Si) and 53 ± 21% (Fe; mean ± SD) of total element concentrations, indicating a substantial contribution of particles to element transport in these European streams, especially for P and Fe. The particulate contents of Fe, Al, and organic C were correlated to their total element concentrations, but those of particulate Si, Mn, P, and Ca were not. The fine colloidal fractions >60 nm were dominated by clay minerals across all sites. The resulting element patterns of NNP <60 nm changed from North to South Europe from Fe- to Ca-dominated particles, along with associated changes in acidity, forest type, and dominant lithology.
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33.
  • Grasset, Charlotte, et al. (författare)
  • Decreasing Photoreactivity and Concurrent Change in Dissolved Organic Matter Composition With Increasing Inland Water Residence Time
  • 2024
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 38:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Photochemical degradation of dissolved organic matter (DOM) has been the subject of numerous studies; however, its regulation along the inland water continuum is still unclear. We aimed to unravel the DOM photoreactivity and concurrent DOM compositional changes across 30 boreal aquatic ecosystems including peat waters, streams, rivers, and lakes distributed along a water residence time (WRT) gradient. Samples were subjected to a standardized exposure of simulated sunlight. We measured the apparent quantum yield (AQY), which corresponds to DOM photomineralization per photon absorbed, and the compositional change in DOM at bulk and individual compound levels in the original samples and after irradiation. AQY increased with the abundance of terrestrially derived DOM and decreased at higher WRT. Additionally, the photochemical changes in both DOM optical properties and molecular composition resembled changes along the natural boreal WRT gradient at low WRT (<3 years). Accordingly, mass spectrometry revealed that the abundance of photolabile and photoproduced molecules decreased with WRT along the boreal aquatic continuum. Our study highlights the tight link between DOM composition and DOM photodegradation. We suggest that photodegradation is an important driver of DOM composition change in waters with low WRT, where DOM is highly photoreactive.
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34.
  • Guo, Laodong, et al. (författare)
  • Characterization of Siberian Arctic coastal sediments : implications for terrestrial organic carbon export
  • 2004
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 18:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Surface sediments were collected during the 2000 TransArctic Expedition along the Siberian Arctic coastline, including the Ob, Yenisey, Khatanga, Lena, and Indigirka estuaries. Sediments were characterized for elemental composition (total organic carbon, TOC, black carbon, BC, and total N, as well as major and trace elements), isotopic signature (δ13C, δ15N, Δ14C, ɛNd, 87Sr/86Sr), and organic molecular composition to better understand river export variations over the large spatial scale of the Siberian Arctic. On average, 79 ± 9% of the total C in sediments was organic while 21 ± 9% was inorganic. BC made up 9 ± 4% of the TOC pool, with a general increasing trend from west to east along the Siberian coast. The combined Nd- and Sr-isotopes (ɛNd and 87Sr/86Sr) were used to define two distinct sediment sources between east and west Siberian regions with the Khatanga River as a boundary. Data from pyrolysis-GC/MS of the sedimentary organic carbon (SOC) indicated an increase in the freshness of the organic matter from west to east on the Siberian Arctic coast, with increasing relative abundance of furfurals (polysaccharides) with respect to nitriles. Values for the δ13C of SOC ranged from -27.1‰ (mostly terrigenous) to -23.8‰, while δ15N increased from east to west (3.1 to 5.2‰) with a significant correlation with C/N ratio. Values for the Δ14C of SOC ranged from -805 to -279‰, with a consistent trend increasing from the east (Indigirka River) to the west (Ob River). These Δ14C values corresponded to a 14C age of 2570 ± 30 yBP in the Ob estuary and 13,050 ± 50 yBP in the Indigirka estuary. Most importantly, Δ14C values were significantly correlated with the ratio of BC/TOC (R2 = 0.91, n = 6), consistent with the distribution pattern of increasing permafrost zone from the west to the east along the Siberian coast. Together, our results suggest that older OC was derived from the release of recalcitrant BC during permafrost thawing and riverbank and coastal erosion, likely enhanced by ongoing environmental changes in the northern ecosystem
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35.
  • Gustafsson, Erik, et al. (författare)
  • External total alkalinity loads versus internal generation : The influence of nonriverine alkalinity sources in the Baltic Sea
  • 2014
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 28:11, s. 1358-1370
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study we first present updated riverine total alkalinity (TA) loads to the various Baltic Sea sub-basins, based on monthly measurements in 82 of the major rivers that represent 85% of the total runoff. Simulations in the coupled physical-biogeochemical BALTSEM (BAltic sea Long-Term large Scale Eutrophication Model) model show that these river loads together with North Sea water inflows are not sufficient to reproduce observed TA concentrations in the system, demonstrating the large influence from internal sources. Budget calculations indicate that the required internal TA generation must be similar to river loads in magnitude. The nonriverine source in the system amounts to about 2.4mmolm(-2) d(-1) on average. We argue here that the majority of this source is related to denitrification together with unresolved sediment processes such as burial of reduced sulfur and/or silicate weathering. This hypothesis is supported by studies on sediment processes on a global scale and also by data from sediment cores in the Baltic Sea. In a model simulation with all internal TA sources and sinks switched on, the net absorption of atmospheric CO2 increased by 0.78mol C m(-2) yr(-1) compared to a simulation where TA was treated as a passive tracer. Our results clearly illustrate how pelagic TA sources together with anaerobic mineralization in coastal sediments generate a significant carbon sink along the aquatic continuum, mitigating CO2 evasions from coastal and estuarine systems.
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36.
  • Hagedorn, Frank, et al. (författare)
  • Elevated atmospheric CO(2) fuels leaching of old dissolved organic matter at the alpine treeline
  • 2008
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 22:2, s. GB2004-
  • Tidskriftsartikel (refereegranskat)abstract
    • Dissolved organic matter (DOM), the mobile form of soil organic matter (SOM), plays an important role in soil C cycling and in nutrient transport. We investigated the effects of 5 years of CO(2) enrichment (370 versus 570 mu mol CO(2) mol(-1)) on DOM dynamics at the alpine treeline, including the analysis of fast-cycling components such as low molecular weight organic acids (LMWOAs), dissolved organic carbon (DOC) biodegradability, and the decomposition of (14)C-labeled oxalate. Concentrations of DOC in canopy throughfall were 20% higher at elevated CO(2), probably driven by higher carbohydrate concentrations in leaves. In the organic soil layer, 5 years of CO(2) enrichment increased water-extractable organic C by 17% and soil solution DOC at 5 cm depth by 20%. The (13)C tracing of recently assimilated CO(2) revealed that the input of recent plant-derived C (< 15% of total DOC) was smaller than the CO(2)-induced increase in DOC. This strongly suggests that CO(2) enrichment enhanced the mobilization of native DOC, which is supported by significant increases in dissolved organic nitrogen (DON). We mainly attribute these increases to a stimulated microbial activity as indicated by higher basal and soil respiration rates (+27%). The (14)C-labeled oxalate was more rapidly mineralized from high CO(2) soils. The concentrations of LMWOAs, but also those of "hydrophilic'' DOC and biodegradable DOC (6% of total DOC), were, however, not affected by elevated CO(2), suggesting that production and consumption of "labile'' DOC were in balance. In summary, our data suggest that 5 years of CO(2) enrichment speeded up the cycling of "labile'' DOM and SOM in a late successional treeline ecosystem and increased the mobilization of older DOM through a stimulated microbial activity. Such a "priming effect'' implies that elevated CO(2) can accelerate the turnover of native SOM, and thus, it may induce increasing losses of old C from thick organic layers.
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37.
  • Harrison, John A., et al. (författare)
  • Global importance, patterns, and controls of dissolved silica retention in lakes and reservoirs
  • 2012
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 26:2, s. n/a-n/a
  • Tidskriftsartikel (refereegranskat)abstract
    • Lentic water bodies (lakes and reservoirs) offer favorable conditions for silica (SiO2) burial in sediments. Recent global estimates suggest that (1) lentic SiO2 trapping is a globally important SiO2 flux, and (2) through reservoir construction, humans have dramatically altered river dissolved SiO2 (DSi) transport and coastal DSi delivery. However, regional to global scale patterns and controls of DSi removal in lentic systems are poorly constrained. Here we use 27 published lake and reservoir DSi budgets to develop insights into patterns and controls of lentic DSi retention and to develop a new, spatially explicit, global model of lentic DSi removal called SiRReLa (Silica Retention in Reservoirs and Lakes). In our analysis, lentic DSi removal (kg SiO2 yr−1) was significantly and positively related to DSi loading (P < 0.0001; r2 = 0.98), and DSi removal efficiency was significantly and positively related to water residence time (P < 0.0001; r2 = 0.68). In addition, DSi settling rates were, on average, 6.5-fold higher in eutrophic systems than in non-eutrophic systems (median settling velocities: 11.1 and 1.7 m yr−1 for eutrophic and non-eutrophic systems, respectively; P < 0.01). SiRReLa, which incorporates these insights, performed quite well in predicting both total DSi removal (kg SiO2 yr−1; Nash Sutcliffe Efficiency (N.S.E) = 0.88) and DSi removal efficiency (% Si removed; N.S.E. = 0.75), with no detectable bias in the model. Global application of SiRReLa confirms that lentic systems are important sinks for DSi, removing 89.1 Tg DSi yr−1 from watersheds globally, roughly 19–38% of all DSi inputs to surface waters. Small lakes and reservoirs (<50 km2) were critical in the analysis, retaining 81% (72 Tg DSi yr−1) of the globally retained total. Furthermore, although reservoirs occupy just 6% of the global lentic surface area, they retained approximately 35% of the total DSi removed by lentic systems. Regional hot spots for lentic DSi removal were identified and imply that lentic systems can remove the vast majority of DSi across a large fraction of Earth's land surface. Finally, a sensitivity analysis indicates that future improvements in DSi trapping and transport models should focus on improving estimates of DSi input to surface waters.
  •  
38.
  • Holmes, M. E., et al. (författare)
  • Carbon Accumulation, Flux, and Fate in Stordalen Mire, a Permafrost Peatland in Transition
  • 2022
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 36:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Stordalen Mire is a peatland in the discontinuous permafrost zone in arctic Sweden that exhibits a habitat gradient from permafrost palsa, to Sphagnum bog underlain by permafrost, to Eriophorum-dominated fully thawed fen. We used three independent approaches to evaluate the annual, multi-decadal, and millennial apparent carbon accumulation rates (aCAR) across this gradient: seven years of direct semi-continuous measurement of CO2 and CH4 exchange, and 21 core profiles for 210Pb and 14C peat dating. Year-round chamber measurements indicated net carbon balance of −13 ± 8, −49 ± 15, and −91 ± 43 g C m−2 y−1 for the years 2012–2018 in palsa, bog, and fen, respectively. Methane emission offset 2%, 7%, and 17% of the CO2 uptake rate across this gradient. Recent aCAR indicates higher C accumulation rates in surface peats in the palsa and bog compared to current CO2 fluxes, but these assessments are more similar in the fen. aCAR increased from low millennial-scale levels (17–29 g C m−2 y−1) to moderate aCAR of the past century (72–81 g C m−2 y−1) to higher recent aCAR of 90–147 g C m−2 y−1. Recent permafrost collapse, greater inundation and vegetation response has made the landscape a stronger CO2 sink, but this CO2 sink is increasingly offset by rising CH4 emissions, dominated by modern carbon as determined by 14C. The higher CH4 emissions result in higher net CO2-equivalent emissions, indicating that radiative forcing of this mire and similar permafrost ecosystems will exert a warming influence on future climate.
  •  
39.
  • Hugelius, Gustaf, 1980-, et al. (författare)
  • Landscape partitioning and environmental gradient analyses of soil organic carbon in a permafrost environment
  • 2009
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 23:GB3006
  • Tidskriftsartikel (refereegranskat)abstract
    • This study investigates landscape allocation and environmental gradients in soil organic carbon (C) storage in northeastern European Russia. The lowlands of the investigated Usa River Basin range from taiga with isolated permafrost to tundra vegetation on continuous permafrost. We compile and analyze databases on soil properties, permafrost, vegetation, and modeled climate. Mean soil C storage is estimated at 38.3 kg C m−2, with similar amounts in taiga and tundra regions. Permafrost soils hold 42% of the total soil C in the area. Peatlands dominate soil C storage with 72% of the total pool and 98% of permafrost C. Multivariate gradient analyses show that local vegetation and permafrost are strong predictors of soil chemical properties, overshadowing the effect of climate variables. This study highlights the importance of peatlands, particularly bogs, in bulk soil C storage. Soil organic matter stored in permafrost has higher C:N ratios than unfrozen material. Permafrost bogs constitute the main vulnerable C pool in the region. Remobilization of this frozen C can occur through gradual but widespread deepening of the active layer with subsequent talik formation or through more rapid but localized thermokarst erosion.
  •  
40.
  • Hugelius, Gustaf (författare)
  • Spatial upscaling using thematic maps : an analysis of uncertainties in permafrost soil carbon estimates
  • 2012
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 26, s. GB2026-
  • Tidskriftsartikel (refereegranskat)abstract
    • Studies of periglacial regions confirm their importance in the global carbon (C) cycle, but estimates of ecosystem C storage or green-house gas fluxes from these remote areas are generally poorly constrained and quantitative estimates of upscaling uncertainties are lacking. In this study, a regional database describing soil organic carbon (SOC) storage in periglacial terrain (European Russian Arctic) was used to evaluate spatial upscaling from point measurements using thematic maps. The selection of classes for upscaling and the need for replication in soil sampling were statistically evaluated. Upscaling using a land cover classification and a soil map estimated SOC storage to 48.5 and 47.0 kg C m(-2), respectively with 95% confidence intervals (CI) within +/- 8%. When corrected for spatial errors in the LCC upscaling proxy, SOC was estimated to 46.5 kg C m(-2) with a 95% CI reflecting propagated variance from both natural variability and spatial errors of +/- 11%. Artificially decreasing the size of the database used for upscaling showed that relatively stable results could be achieved with lower replication in some upscaling classes. Decreased spatial resolution for upscaling from 30 m to 1 km had little impact on SOC estimates in this region, but classification accuracy was dramatically reduced and land cover classes show different, sometimes nonlinear, responses to scale. The methods and recommendations presented here can provide guidelines for any future study where point observations of a variable are upscaled using remotely sensed thematic maps or classifications and potential applications for circum-arctic studies are discussed. For future upscaling studies at large geographic scales, a priori determination of sample sizes and tests to insure unimodal and statistically independent samples are recommended. If these prerequisites are not fulfilled, classes may be merged or subdivided prior to upscaling.
  •  
41.
  • Humborg, Christoph, et al. (författare)
  • Sea-air exchange patterns along the central and outer East Siberian Arctic Shelf as inferred from continuous CO2, stable isotope, and bulk chemistry measurements
  • 2017
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 31:7, s. 1173-1191
  • Tidskriftsartikel (refereegranskat)abstract
    • This large-scale quasi-synoptic study gives a comprehensive picture of sea-air CO 2 fluxes during the melt season in the central and outer Laptev Sea (LS) and East Siberian Sea (ESS). During a 7 week cruise we compiled a continuous record of both surface water and air CO 2 concentrations, in total 76,892 measurements. Overall, the central and outer parts of the ESAS constituted a sink for CO 2 , and we estimate a median uptake of 9.4 g C m -2 yr -1 or 6.6 Tg C yr -1 . Our results suggest that while the ESS and shelf break waters adjacent to the LS and ESS are net autotrophic systems, the LS is a net heterotrophic system. CO 2 sea-air fluxes for the LS were 4.7 g C m -2 yr -1 , and for the ESS we estimate an uptake of 7.2 g C m -2 yr -1 . Isotopic composition of dissolved inorganic carbon (δ 13 C DIC and δ 13 C CO2 ) in the water column indicates that the LS is depleted in δ 13 C DIC compared to the Arctic Ocean (ArcO) and ESS with an offset of 0.5‰ which can be explained by mixing of δ 13 C DIC -depleted riverine waters and 4.0 Tg yr -1 respiration of OC ter ; only a minor part (0.72 Tg yr -1 ) of this respired OC ter is exchanged with the atmosphere. Property-mixing diagrams of total organic carbon and isotope ratio (δ 13 C SPE-DOC ) versus dissolved organic carbon (DOC) concentration diagram indicate conservative and nonconservative mixing in the LS and ESS, respectively. We suggest land-derived particulate organic carbon from coastal erosion as an additional significant source for the depleted δ 13 C DIC .
  •  
42.
  • Häggi, C., et al. (författare)
  • Negligible Quantities of Particulate Low-Temperature Pyrogenic Carbon Reach the Atlantic Ocean via the Amazon River
  • 2021
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 35:9
  • Tidskriftsartikel (refereegranskat)abstract
    • Particulate pyrogenic carbon (PyC) transported by rivers and aerosols, and deposited in marine sediments, is an important part of the carbon cycle. The chemical composition of PyC is temperature dependent and levoglucosan is a source-specific burning marker used to trace low-temperature PyC. Levoglucosan associated to particulate material has been shown to be preserved during riverine transport and marine deposition in high- and mid-latitudes, but it is yet unknown if this is also the case for (sub)tropical areas, where 90% of global PyC is produced. Here, we investigate transport and deposition of levoglucosan in suspended and riverbed sediments from the Amazon River system and adjacent marine deposition areas. We show that the Amazon River exports negligible amounts of levoglucosan and that concentrations in sediments from the main Amazon tributaries are not related to long-term mean catchment-wide fire activity. Levoglucosan concentrations in marine sediments offshore the Amazon Estuary are positively correlated to total organic content regardless of terrestrial or marine origin, supporting the notion that association of suspended or dissolved PyC to biogenic particles is critical in the preservation of PyC. We estimate that 0.5-10 x 10(6) g yr(-1) of levoglucosan is exported by the Amazon River. This represents only 0.5-10 ppm of the total exported PyC and thereby an insignificant fraction, indicating that riverine derived levoglucosan and low-temperature PyC in the tropics are almost completely degraded before deposition. Hence, we suggest caution in using levoglucosan as tracer for past fire activity in tropical settings near rivers.
  •  
43.
  • Isles, Peter D. F., et al. (författare)
  • Recent Synchronous Declines in DIN:TP in Swedish Lakes
  • 2018
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 32:2, s. 208-225
  • Tidskriftsartikel (refereegranskat)abstract
    • Declining atmospheric nitrogen (N) deposition in northern Europe and parts of North America, coupled with ongoing changes in climate, has the potential to alter the nutrient limitation status of freshwater ecosystems. In this study we compared time series data of atmospheric N deposition, air temperature, and precipitation with corresponding estimates of dissolved inorganic nitrogen (DIN), total phosphorus (TP), DIN: TP, and total organic carbon from 78 headwater streams and 95 nutrient-poor lakes in Sweden from 1998 to 2013 to assess trends in, and potential drivers of, lake N:P ratios. We found that trends in nutrients were variable at the scale of individual lakes but were highly synchronous at the regional scale, suggesting underlying control by broad-scale environmental drivers mediated by site-specific characteristics. Widespread declines in lake DIN throughout Sweden were correlated with declines in atmospheric N deposition, particularly in northern areas. TP did not have strong directional trends, but interannual variability was synchronous at regional scales, implying that broad-scale climate drivers were affecting these trends. Overall, we observed a significant decline in DIN:TP throughout Sweden over the monitoring period. At the beginning of the study period, 32% of lakes were N limited and 45% colimited by N and P. Proportions increased to 63% of lakes N limited and 20% colimited by N and P at the end of the study period. These results suggest that N limitation is likely to become more widespread in subarctic and boreal areas of Europe in the future if recent trends continue. Plain Language Summary This article examines the way in which changes in the amount of nitrogen from the atmosphere being delivered to lakes (as a result of fossil fuel combustion) are interacting with global climate change to affect nutrient availability in Swedish lakes. Nitrogen can act as fertilizer in lakes, supporting increased growth of algae and aquatic plants. The amount of nitrogen relative to other important elements such as phosphorus can help to determine which groups of plants and algae dominate lake ecosystems, as well as how much living biomass lakes can sustain. We find that declines in atmospheric deposition of nitrogen, which have resulted from the adoption of policies controlling emissions from fossil fuel combustion, have caused declines in nitrogen concentrations in lakes throughout Sweden. This has changed the balance of nitrogen and phosphorus, which may result in changes to the structure of lake biological communities. At the same time, variability in climate also has subtle but widespread affects on lake nutrient concentrations, suggesting that the availability of nutrients in lakes at northern latitudes is likely to change in the future as the climate warms.
  •  
44.
  • Karlsson, Emma, et al. (författare)
  • Different sources and degradation state of dissolved, particulate, and sedimentary organic matter along the Eurasian Arctic coastal margin
  • 2016
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 30:6, s. 898-919
  • Tidskriftsartikel (refereegranskat)abstract
    • Thawing Arctic permafrost causes massive fluvial and erosional releases of dissolved and particulate organic carbon (DOC and POC) to coastal waters. Here we investigate how different sources and degradation of remobilized terrestrial carbon may affect large-scale carbon cycling, by comparing molecular and dual-isotope composition of waterborne high molecular weight DOC (>1kD, aka colloidal OC), POC, and sedimentary OC (SOC) across the East Siberian Arctic Shelves. Lignin phenol fingerprints demonstrate a longitudinal trend in relative contribution of terrestrial sources to coastal OC. Wax lipids and cutins were not detected in colloidal organic carbon (COC), in contrast to POC and SOC, suggesting that different terrestrial carbon pools partition into different aquatic carrier phases. The C-14 signal suggests overwhelmingly contemporary sources for COC, while POC and SOC are dominated by old C from Ice Complex Deposit (ICD) permafrost. Monte Carlo source apportionment (C-13, C-14) constrained that COC was dominated by terrestrial OC from topsoil permafrost (65%) and marine plankton (25%) with smaller contribution ICD and other older permafrost stocks (9%). This distribution is likely a result of inherent compositional matrix differences, possibly driven by organomineral associations. Modern OC found suspended in the surface water may be more exposed to degradation, in contrast to older OC that preferentially settles to the seafloor where it may be degraded on a longer timescale. The different sources which partition into DOC, POC, and SOC appear to have vastly different fates along the Eurasian Arctic coastal margin and may possibly respond on different timescales to climate change.
  •  
45.
  • Khalili, Maria, et al. (författare)
  • Nitrogen and carbon interactions between boreal soils and lakes
  • 2010
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 24
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, we used a large data set on nitrogen (N) and carbon (C) from Swedish boreal soils and lake waters to investigate N and C interactions between soils and lake waters. To link thousands of soils sites with hundreds of lake sites distributed all over Sweden, we gridded the data and found a significant relation between gridded C:N ratios of the organic soil layer and the ones of lake waters. We also found evidence of N deposition having depressed the C:N ratios of lake waters more than the ones of organic soil layers. In lake waters N strongly increased toward southern Sweden, mainly in the form of nitrate-nitrogen (NO(3)(-)-N) which we primarily attribute to an increased NO(3)(-)-N input from the boreal soils into the lakes. In contrast to N we found a much weaker direct relationship for C between soils and lake waters over Sweden. Instead, lake C was strongly related to lake morphometry and catchment characteristics. Our results indicate that large-scale variations in soil C content are not directly linked to C concentrations in lake waters, whereas soil N seems to leach in small amounts from the soils directly into the lakes in form of NO(3)(-)-N. Such differences in N and C interactions between soils and lake waters give important insights into the global biogeochemical cycling of N and C.
  •  
46.
  • Klaus, Marcus, et al. (författare)
  • Evaluations of Climate and Land Management Effects on Lake Carbon Cycling Need to Account Temporal Variability in CO2 Concentration
  • 2019
  • Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 33:3, s. 243-265
  • Tidskriftsartikel (refereegranskat)abstract
    • Carbon dioxide (CO2) concentrations in lakes vary strongly over time. This variability is rarely captured by environmental monitoring but is crucial for accurately assessing the magnitude of lake CO2 emissions. However, it is unknown to what extent temporal variability needs to be captured to understand important drivers of lake carbon cycling such as climate and land management. We used environmental monitoring data of Swedish forest lakes collected in autumn (n = 439) and throughout the whole open water season (n = 22) from a wet and a dry year to assess temporal variability in effects of climate and forestry on CO2 concentrations across lakes. Effects differed depending on the season and year sampled. According to cross-lake comparisons based on autumn data, CO2 concentrations increased with annual mean air temperature (dry year) or catchment forest productivity (wet year) but were not related to colored dissolved organic matter concentrations. In contrast, open water-season averaged CO2 concentrations were similar across temperature and productivity gradients but increased with colored dissolved organic matter. These contradictions resulted from scale mismatches in input data, lead to weak explanatory power (R-2 = 9-32%), and were consistent across published data from 79 temperate, boreal, and arctic lakes. In a global survey of 144 published studies, we identified a trade-off between temporal and spatial coverage of CO2 sampling. This trade-off clearly determines which conclusions are drawn from landscape-scale CO(2 )assessments. Accurate evaluations of the effects of climate and land management require spatially and temporally representative data that can be provided by emerging sensor technologies and forms of collaborative sampling.
  •  
47.
  • Koehler, Birgit, 1980-, et al. (författare)
  • Sunlight-induced carbon dioxide emissions from inland waters
  • 2014
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 28:7, s. 696-711
  • Tidskriftsartikel (refereegranskat)abstract
    • The emissions of carbon dioxide (CO2) from inland waters are substantial on a global scale. Yet, the fundamental question remains open which proportion of these CO2 emissions is induced by sunlight via photochemical mineralization of dissolved organic carbon (DOC), rather than by microbial respiration during DOC decomposition. Also, it is unknown on larger spatial and temporal scales how photochemical mineralization compares to other C fluxes in the inland water C cycle. We combined field and laboratory data with atmospheric radiative transfer modeling to parameterize a photochemical rate model for each day of the year 2009, for 1086 lakes situated between latitudes from 55 to 69°N in Sweden. The sunlight-induced production of dissolved inorganic carbon (DIC) averaged 3.8 ± 0.04 g C m-2 yr-1, which is a flux comparable in size to the organic carbon burial in the lake sediments. Countrywide, 151 ± 1 kt C yr-1 was produced by photochemical mineralization, corresponding to about 12% of total annual mean CO2 emissions from Swedish lakes. With a median depth of 3.2 m, the lakes were generally deep enough that incoming, photochemically active photons were absorbed in the water column. This resulted in a linear positive relationship between DIC photoproduction and the incoming photon flux, which correspond to the absorbed photons. Therefore, the slope of the regression line represents the wavelength- and depth-integrated apparent quantum yield of DIC photoproduction. We used this relationship to obtain a first estimate of DIC photoproduction in lakes and reservoirs worldwide. Global DIC photoproduction amounted to 13 and 35 Mt C yr-1 under overcast and clear sky, respectively. Consequently, these directly sunlight-induced CO2 emissions contribute up to about one tenth to the global CO2 emissions from lakes and reservoirs, corroborating that microbial respiration contributes a substantially larger share than formerly thought, and generate annual C fluxes similar in magnitude to the C burial in natural lake sediments worldwide.
  •  
48.
  • Kronberg, Rose-Marie, et al. (författare)
  • Forest harvest contribution to Boreal freshwater methyl mercury load
  • 2016
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 30:6, s. 825-843
  • Tidskriftsartikel (refereegranskat)abstract
    • Effects of Boreal forest harvest on mercury (Hg) and methyl mercury (MeHg) soil pools and export by stream runoff were quantified by comparing 10 reference watersheds (REFs) covered by >80year old Norway spruce (Picea abies Karst.) forests with 10 similar watersheds subjected to clear-cutting (CCs). While total Hg soil storage did not change, MeHg pools increased seven times (p=0.006) in the organic topsoil 2 years after clear-cutting. In undulating terrain, situated above the postglacial marine limit (ML) of the ancient Baltic Sea, the mass ratio between flux-weighted MeHg and dissolved organic carbon (MeHg/DOC) in stream runoff increased 1.8 times (p<0.004) as a consequence of forest harvest. When recalculated to 100% clear-cutting of the watershed, the annual MeHg stream export increased 3.8 times (p=0.047). Below the ML, where the terrain was flatter, neither the MeHg/DOC ratio nor the annual export of MeHg differed between REFs and CCs, likely because of the larger contribution of MeHg exported from peaty soils and small wetlands. The most robust measure, MeHg/DOC, was used to calculate MeHg loadings to Boreal headwaters. If the forest harvest effect lasts 10years, clear-cutting increases MeHg runoff by 12-20% in Sweden and 2% in the Boreal zone as a whole. In Sweden, having intensely managed forests, 37% and 56% of MeHg are exported from peatlands and forest soils, respectively, and forest clear-cutting is adding another 6.6%. In the Boreal zone as a whole peatlands and forests soils contribute with 53% and 46%, respectively, and clear-cutting is estimated to add another 1.0%. An expected rapid increase in Boreal forest harvest and disturbance urge for inclusion of land use effects in mercury biogeochemical cycling models at different scales.
  •  
49.
  • Laruelle, G. G., et al. (författare)
  • Anthropogenic perturbations of the silicon cycle at the global scale: Key role of the land-ocean transition
  • 2009
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 23
  • Forskningsöversikt (refereegranskat)abstract
    • Silicon (Si), in the form of dissolved silicate (DSi), is a key nutrient in marine and continental ecosystems. DSi is taken up by organisms to produce structural elements (e.g., shells and phytoliths) composed of amorphous biogenic silica (bSiO(2)). A global mass balance model of the biologically active part of the modern Si cycle is derived on the basis of a systematic review of existing data regarding terrestrial and oceanic production fluxes, reservoir sizes, and residence times for DSi and bSiO(2). The model demonstrates the high sensitivity of biogeochemical Si cycling in the coastal zone to anthropogenic pressures, such as river damming and global temperature rise. As a result, further significant changes in the production and recycling of bSiO(2) in the coastal zone are to be expected over the course of this century.
  •  
50.
  • Laudon, Hjalmar, et al. (författare)
  • Linking variability in soil solution dissolved organic carbon to climate, soil type, and vegetation type
  • 2014
  • Ingår i: Global Biogeochemical Cycles. - 0886-6236 .- 1944-9224. ; 28, s. 497-509
  • Tidskriftsartikel (refereegranskat)abstract
    • Lateral transport of carbon plays an important role in linking the carbon cycles of terrestrial and aquatic ecosystems. There is, however, a lack of information on the factors controlling one of the main C sources of this lateral flux, i.e., the concentration of dissolved organic carbon (DOC) in soil solution across large spatial scales and under different soil, vegetation, and climate conditions. We compiled a database on DOC in soil solution down to 80cm and analyzed it with the aim, first, to quantify the differences in DOC concentrations among terrestrial ecosystems, climate zones, soil, and vegetation types at global scale and second, to identify potential determinants of the site-to-site variability of DOC concentration in soil solution across European broadleaved and coniferous forests. We found that DOC concentrations were 75% lower in mineral than in organic soil, and temperate sites showed higher DOC concentrations than boreal and tropical sites. The majority of the variation (R2=0.67-0.99) in DOC concentrations in mineral European forest soils correlates with NH4+, C/N, Al, and Fe as the most important predictors. Overall, our results show that the magnitude (23% lower in broadleaved than in coniferous forests) and the controlling factors of DOC in soil solution differ between forest types, with site productivity being more important in broadleaved forests and water balance in coniferous stands.
  •  
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