| 1. |
- Audet, J., et al.
(författare)
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Forest streams are important sources for nitrous oxide emissions
- 2020
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Ingår i: Global Change Biology. - : Wiley. - 1354-1013 .- 1365-2486. ; 26:2, s. 629-641
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Tidskriftsartikel (refereegranskat)abstract
- Streams and river networks are increasingly recognized as significant sources for the greenhouse gas nitrous oxide (N2O). N2O is a transformation product of nitrogenous compounds in soil, sediment and water. Agricultural areas are considered a particular hotspot for emissions because of the large input of nitrogen (N) fertilizers applied on arable land. However, there is little information on N2O emissions from forest streams although they constitute a major part of the total stream network globally. Here, we compiled N2O concentration data from low-order streams (~1,000 observations from 172 stream sites) covering a large geographical gradient in Sweden from the temperate to the boreal zone and representing catchments with various degrees of agriculture and forest coverage. Our results showed that agricultural and forest streams had comparable N2O concentrations of 1.6 ± 2.1 and 1.3 ± 1.8 µg N/L, respectively (mean ± SD) despite higher total N (TN) concentrations in agricultural streams (1,520 ± 1,640 vs. 780 ± 600 µg N/L). Although clear patterns linking N2O concentrations and environmental variables were difficult to discern, the percent saturation of N2O in the streams was positively correlated with stream concentration of TN and negatively correlated with pH. We speculate that the apparent contradiction between lower TN concentration but similar N2O concentrations in forest streams than in agricultural streams is due to the low pH (<6) in forest soils and streams which affects denitrification and yields higher N2O emissions. An estimate of the N2O emission from low-order streams at the national scale revealed that ~1.8 × 109 g N2O-N are emitted annually in Sweden, with forest streams contributing about 80% of the total stream emission. Hence, our results provide evidence that forest streams can act as substantial N2O sources in the landscape with 800 × 109 g CO2-eq emitted annually in Sweden, equivalent to 25% of the total N2O emissions from the Swedish agricultural sector. © 2019 The Authors. Global Change Biology published by John Wiley & Sons Ltd
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| 2. |
- Barros, Nathan, et al.
(författare)
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Carbon emission from hydroelectric reservoirs linked to reservoir age and latitude
- 2011
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Ingår i: Nature Geoscience. - : Nature Publishing Group. - 1752-0894 .- 1752-0908. ; 4:9, s. 593-596
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Tidskriftsartikel (refereegranskat)abstract
- Hydroelectric reservoirs cover an area of 3.4 x 10(5) km(2) and comprise about 20% of all reservoirs. In addition, they contain large stores of formerly terrestrial organic carbon. Significant amounts of greenhouse gases are emitted(2), especially in the early years following reservoir creation, but the global extent of these emissions is poorly known. Previous estimates of emissions from all types of reservoir indicate that these human-made systems emit 321 Tg of carbon per year (ref. 4). Here we assess the emissions of carbon dioxide and methane from hydroelectric reservoirs, on the basis of data from 85 globally distributed hydroelectric reservoirs that account for 20% of the global area of these systems. We relate the emissions to reservoir age, location biome, morphometric features and chemical status. We estimate that hydroelectric reservoirs emit about 48 Tg C as CO(2) and 3 Tg C as CH(4), corresponding to 4% of global carbon emissions from inland waters. Our estimates are smaller than previous estimates on the basis of more limited data. Carbon emissions are correlated to reservoir age and latitude, with the highest emission rates from the tropical Amazon region. We conclude that future emissions will be highly dependent on the geographic location of new hydroelectric reservoirs.
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| 3. |
- Bastviken, David, et al.
(författare)
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Degradation of dissolved organic matter in oxic and anoxic lake water
- 2004
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Ingår i: Limnology and Oceanography. - : John Wiley & Sons. - 0024-3590 .- 1939-5590. ; 49:1, s. 109–116-
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Tidskriftsartikel (refereegranskat)abstract
- Decades of conflicting results have fueled a debate about how O-2 affects organic matter (OM) degradation and carbon cycling. In a laboratory study, using both OM taken directly from a humic lake and chemically isolated fulvic acid, we monitored the mineralization of dissolved OM in freshwater under purely oxic and anoxic conditions, under oxic then anoxic conditions, and under anoxic then oxic conditions, for 426 d. Between 5% and 24% of the initial OM was mineralized, with most extensive mineralization occurring under purely oxic and anoxic-oxic conditions. A sequential change in the O-2 regime did not result in greater overall degradation, but initially anoxic conditions favored subsequent oxic mineralization. A substantially greater fraction of the OM was degraded than in previous shorter studies, with as much as 50% of the total OM degradation occurring after 147 d into the experiment. Three fractions of the degradable OM were identified: OM degraded only under oxic conditions (68-78%), OM degraded more rapidly under anoxic conditions than under oxic conditions (16-18%), and OM degraded at equal rates under both oxic and anoxic conditions (6-14%). The degradation patterns of natural dissolved OM from a humic lake and chemically isolated fulvic acid were very similar, which indicates a similar level of bioavailability. The difference between anoxic and oxic degradation was greater in our long-term studies than in previous short-term experiments, which indicates that the oxic and anoxic degradation potentials vary with increasing overall OM recalcitrance and that similar oxic and anoxic degradation rates can be expected in short-term experiments in which <30% of the long-term degradable OM is allowed to decompose.
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| 4. |
- Bastviken, David, et al.
(författare)
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Freshwater Methane Emissions Offset the Continental Carbon Sink
- 2011
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Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 331:6013, s. 50-50
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Tidskriftsartikel (refereegranskat)abstract
- Inland waters (lakes, reservoirs, streams, and rivers) are often substantial methane (CH4) sources in the terrestrial landscape. They are, however, not yet well integrated in global greenhouse gas (GHG) budgets. Data from 474 freshwater ecosystems and the most recent global water area estimates indicate that freshwaters emit at least 103 teragrams of CH4 year−1, corresponding to 0.65 petagrams of C as carbon dioxide (CO2) equivalents year−1, offsetting 25% of the estimated land carbon sink. Thus, the continental GHG sink may be considerably overestimated, and freshwaters need to be recognized as important in the global carbon cycle.
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| 5. |
- Bastviken, David, et al.
(författare)
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Methane emissions from lakes : Dependence of lake characteristics, two regional assessments, and a global estimate
- 2004
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Ingår i: Global Biogeochemical Cycles. - : Wiley-Blackwell Publishing Inc.. - 0886-6236 .- 1944-9224. ; 18, s. GB4009-
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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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| 6. |
- Chmiel, Hannah Elisa, 1983-, et al.
(författare)
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The role of sediments in the carbon budget of a small boreal lake
- 2016
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Ingår i: Limnology and Oceanography. - : Wiley. - 0024-3590 .- 1939-5590. ; 61:5, s. 1814-1825
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Tidskriftsartikel (refereegranskat)abstract
- We investigated the role of lake sediments as carbon (C) source and sink in the annual C budget of a small (0.07 km2), shallow (mean depth 3.4 m), and humic lake (mean DOC concentration 17 mg L-1) in boreal Sweden. Organic carbon (OC) burial and mineralization in sediments were quantified from 210Pb-dated sediment and laboratory sediment incubation experiments, respectively, and upscaled to the entire basin and to one whole year, by using sediment thickness derived sub-bottom profiling, basin morphometry, and water column monitoring data of temperature and oxygen concentration. Furthermore, catchment C import, open water metabolism, photochemical mineralization as well as carbon dioxide (CO2) and methane (CH4) emissions to the atmosphere, were quantified to relate sediment processes to other lake C fluxes. We found that on a whole-basin and annual scale, sediment OC mineralization was three times larger than OC burial, and contributed about 16% to the annual CO2 emission from the lake to the atmosphere. Remaining contributions to the CO2 emission were attributed to water column metabolism (31%), photochemical mineralization (6%), and catchment imports via inlet streams and inflow of shallow groundwater (47%). We conclude that on an annual and whole-basin scale 1) sediment OC mineralization dominated over OC burial, 2) water column OC mineralization contributed more than sediments to lake CO2 emission, and 3) catchment import of C to the lake was greater than lake-internal C cycling.
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| 7. |
- Denfeld, Blaize A., et al.
(författare)
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Constraints on methane oxidation in ice-covered boreal lakes
- 2016
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Ingår i: Journal of Geophysical Research - Biogeosciences. - : AMER GEOPHYSICAL UNION. - 2169-8953 .- 2169-8961. ; 121:7, s. 1924-1933
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Tidskriftsartikel (refereegranskat)abstract
- Boreal lakes can be ice covered for a substantial portion of the year at which time methane (CH4) can accumulate below ice. The amount of CH4 emitted at ice melt is partially determined by the interplay between CH4 production and CH4 oxidation, performed by methane-oxidizing bacteria (MOB). Yet the balance between oxidation and emission and the potential for CH4 oxidation in various lakes during winter is largely unknown. To address this, we performed incubations at 2 degrees C to screen for wintertime CH4 oxidation potential in seven lakes. Results showed that CH4 oxidation was restricted to three lakes, where the phosphate concentrations were highest. Molecular analyses revealed that MOB were initially detected in all lakes, although an increase in type I MOB only occurred in the three lake water incubations where oxidation could be observed. Accordingly, the increase in CO2 was on average 5 times higher in these three lake water incubations. For one lake where no oxidation was measured, we tested if temperature and CH4 availability could trigger CH4 oxidation. However, regardless of incubation temperatures and CH4 concentrations, ranging from 2 to 20 degrees C and 1-500M, respectively, no oxidation was observed. Our study indicates that some lakes with active wintertime CH4 oxidation may have low emissions during ice melt, while other and particularly nutrient poor lakes may accumulate large amounts of CH4 below ice that, in the absence of CH4 oxidation, will be emitted following ice melt. This variability in CH4 oxidation rates between lakes needs to be accounted for in large-scale CH4 emission estimates.
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| 8. |
- Grasset, Charlotte, et al.
(författare)
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Large but variable methane production in anoxic freshwater sediment upon addition of allochthonous and autochthonous organic matter
- 2018
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Ingår i: Limnology and Oceanography. - : Wiley. - 0024-3590 .- 1939-5590. ; 63:4, s. 1488-1501
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Tidskriftsartikel (refereegranskat)abstract
- An important question in the context of climate change is to understand how CH4 production is regulated in anoxic sediments of lakes and reservoirs. The type of organic carbon (OC) present in lakes is a key factor controlling CH4 production at anoxic conditions, but the studies investigating the methanogenic potential of the main OC types are fragmented. We incubated different types of allochthonous OC (alloOC; terrestrial plant leaves) and autochthonous OC (autoOC; phytoplankton and two aquatic plants species) in an anoxic sediment during 130 d. We tested if (1) the supply of fresh alloOC and autoOC to an anoxic refractory sediment would fuel CH4 production and if (2) autoOC would decompose faster than alloOC. The addition of fresh OC greatly increased CH4 production and the δ13C-CH4 partitioning indicated that CH4 originated exclusively from the fresh OC. The large CH4 production in an anoxic sediment fueled by alloOC is a new finding which indicates that all systems with anoxic conditions and high sedimentation rates have the potential to be CH4 emitters. The autoOC decomposed faster than alloOC, but the total CH4 production was not higher for all autoOC types, one aquatic plant species having values as low as the terrestrial leaves, and the other one having values as high as phytoplankton. Our study is the first to report such variability, suggesting that the extent to which C fixed by aquatic plants is emitted as greenhouse gases or buried as OC in sediment could more generally differ between aquatic vegetation types.
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| 9. |
- Gudasz, Cristian, et al.
(författare)
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Constrained microbial processing of allochthonous organic carbon in boreal lake sediments
- 2012
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Ingår i: Limnology and Oceanography. - : Wiley. - 0024-3590 .- 1939-5590. ; 57:1, s. 163-175
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Tidskriftsartikel (refereegranskat)abstract
- We investigated sediment bacterial metabolism in eight lakes with different inputs of allochthonous and autochthonous organic carbon in south-central Sweden. Sediment bacterial production, mineralization and biomass were measured on a seasonal basis and along a lake depth gradient together with different water and sediment characteristics. Sediment bacterial metabolism was primarily controlled by temperature but also regulated by organic carbon quality/origin. Metabolism was positively correlated to measures of autochthonous influence on the sediment organic carbon, but did not show a similar increase with increasing input of allochthonous organic carbon. Hence, in contrast to what is currently known for the water column, increasing amounts of terrestrial organic carbon do not result in enhanced sediment bacterial metabolism. Meio- and macrobenthic invertebrate biomass were at most weakly correlated to bacterial metabolism and biomass, suggesting limited control of sediment bacteria by grazing. We suggest that the bacterial metabolism in boreal lake sediments is constrained by low temperatures and by the recalcitrant nature of the dominant organic carbon, resulting in sediments being an effective sink of organic carbon.
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| 10. |
- Gudasz, Cristian, et al.
(författare)
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Temperature-controlled organic carbon mineralization in lake sediments
- 2010
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Ingår i: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 466:7305, s. 478-481
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Tidskriftsartikel (refereegranskat)abstract
- Peatlands, soils and the ocean floor are well-recognized as sites of organic carbonaccumulation andrepresentimportant global carbon sinks(1,2). Although the annual burial of organic carbon in lakes and reservoirs exceeds that of ocean sediments(3), these inland waters are components of the global carbon cycle that receive only limited attention(4-6). Of the organic carbon that is being deposited onto the sediments, a certain proportion will be mineralized and the remainder will be buried over geological timescales. Here we assess the relationship between sediment organic carbon mineralization and temperature in a cross-system survey of boreal lakes in Sweden, and with input froma compilation of published data from awide range of lakes that differ with respect to climate, productivity and organic carbon source. We find that the mineralization of organic carbon in lake sediments exhibits a strongly positive relationship with temperature, which suggests that warmer water temperatures lead to more mineralization and less organic carbon burial. Assuming that future organic carbon delivery to the lake sediments will be similar to that under present-day conditions, we estimate that temperature increases following the latest scenarios presented by the Intergovernmental Panel on Climate Change(7) could result in a 4-27 per cent (0.9-6.4 Tg Cyr(-1)) decrease in annual organic carbon burial in boreal lakes.
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