| 1. |
- Oni, Stephen, et al.
(författare)
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Local- and landscape-scale impacts of clear-cuts and climate change on surface water dissolved organic carbon in boreal forests
- 2015
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Ingår i: Journal of Geophysical Research - Biogeosciences. - 2169-8953 .- 2169-8961. ; 120:11, s. 2402-2426
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Tidskriftsartikel (refereegranskat)abstract
- Forest harvesting and climate change may significantly increase concentrations and fluxes of dissolved organic carbon (DOC) in boreal surface waters. However, the likely magnitude of any effect will vary depending on the landscape-element type and spatial scale. We used a chain of hydrological, empirical, and process-based biogeochemical models coupled to an ensemble of downscaled Regional Climate Model experiments to develop scenario storylines for local- and landscape-scale effects of forest harvesting and climate change on surface water DOC concentrations and fluxes. Local-scale runoff, soil temperature, and DOC dynamics were simulated for a range of forest and wetland landscape-element types and at the larger landscape scale. The results indicated that climate change will likely lead to greater winter flows and earlier, smaller spring peaks. Both forest harvesting and climate change scenarios resulted in large increases in summer and autumn runoff and higher DOC fluxes. Forest harvesting effects were clearly apparent at local scales. While at the landscape scale, approximately 1 mg L−1 (or 10%) of the DOC in surface waters can be attributed to clear-cuts, both climate change and intensified forestry can each increase DOC concentrations by another 1 mg L−1 in the future, which is less than that seen in many waterbodies recovering from acidification. These effects of forestry and climate change on surface water DOC concentrations are additive at a landscape scale but not at the local scale, where a range of landscape-element specific responses were observed.
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| 2. |
- Klaminder, Jonatan, et al.
(författare)
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Carbon mineralization and pyrite oxidation in groundwater : Importance for silicate weathering in boreal forest soils and stream base-flow chemistry
- 2011
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Ingår i: Applied Geochemistry. - : Elsevier BV. - 0883-2927 .- 1872-9134. ; 26:3, s. 319-324
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Tidskriftsartikel (refereegranskat)abstract
- What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H(2)CO(3), produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and delta(18)O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H2CO3 generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a buildup of SO(4)(2-) in the groundwater during lateral transport and a delta(34)S parts per thousand value of +0.26-3.76 parts per thousand in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km(2)) as evident by delta(18)O signatures and base cation concentrations that overlap with that of the groundwater.
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| 3. |
- Sundman, Anneli, et al.
(författare)
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XAS study of iron speciation in soils and waters from a boreal catchment
- 2014
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Ingår i: Chemical Geology. - : Elsevier. - 0009-2541 .- 1872-6836. ; 364, s. 93-102
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Tidskriftsartikel (refereegranskat)abstract
- Iron (Fe) is a key element, strongly influencing the biogeochemistry of soils, sediments and waters, but the knowledge about the variety of Fe species present in these systems is still limited. In this work we have used X-ray absorption spectroscopy (XAS) to study the speciation of Fe in soils and waters from a boreal catchment in northern Sweden. The aim was to better understand the controls of Fe speciation across different, but adjacent landscape elements including soil, soil solution, groundwater and stream water draining catchments with contrasting land characteristics. Our results showed that all samples contained mixtures of Fe(II) and Fe(III). The soils consisted of Fe phyllosilicates, Fe (hydr)oxides and Fe complexed by natural organic matter (NOM). All aqueous samples contained Fe(II)– and Fe(III)–NOM complexes, often in combination with Fe(III) (hydr)oxides that were associated with NOM. The variation in contribution from Fe–NOM and Fe (hydr)oxides was controlled by pH and total concentrations of NOM. The XAS spectra suggested formation of mononuclear Fe–NOM complexes consisting of chelate ring structures, but it could not be determined whether they originated solely from Fe(III)– or from a mixture of Fe(II)/Fe(III)–NOM complexes. Our collective results showed that the Fe speciation was highly variable across the different landscape elements and streams. This variation was manifested both in the distribution between mononuclear Fe–NOM complexes and Fe (hydr)oxides associated with NOM and between Fe(II) and Fe(III). These results highlight the complexity of Fe speciation in natural environmental systems and thus the challenges in interpreting Fe reactivity.
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| 4. |
- Audet, Joachim, et al.
(författare)
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Forest streams are important sources for nitrous oxide emissions - Nitrous oxide emissions from Swedish streams
- 2020
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Ingår i: Global Change Biology. - : Wiley. - 1354-1013 .- 1365-2486. ; 26, 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 mu g N/L, respectively (mean +/- SD) despite higher total N (TN) concentrations in agricultural streams (1,520 +/- 1,640 vs. 780 +/- 600 mu g 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 x 10(9) 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 x 10(9) g CO2-eq emitted annually in Sweden, equivalent to 25% of the total N2O emissions from the Swedish agricultural sector.
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| 5. |
- Campeau, Audrey, et al.
(författare)
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Current forest carbon fixation fuels stream CO 2 emissions
- 2019
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Ingår i: Nature Communications. - : Nature Publishing Group. - 2041-1723. ; 10:1
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Tidskriftsartikel (refereegranskat)abstract
- Stream CO 2 emissions contribute significantly to atmospheric climate forcing. While there are strong indications that groundwater inputs sustain these emissions, the specific biogeochemical pathways and timescales involved in this lateral CO 2 export are still obscure. Here, via an extensive radiocarbon ( 14 C) characterisation of CO 2 and DOC in stream water and its groundwater sources in an old-growth boreal forest, we demonstrate that the 14 C-CO 2 is consistently in tune with the current atmospheric 14 C-CO 2 level and shows little association with the 14 C-DOC in the same waters. Our findings thus indicate that stream CO 2 emissions act as a shortcut that returns CO 2 recently fixed by the forest vegetation to the atmosphere. Our results expose a positive feedback mechanism within the C budget of forested catchments, where stream CO 2 emissions will be highly sensitive to changes in forest C allocation patterns associated with climate and land-use changes. © 2019, The Author(s).
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| 6. |
- Campeau, Audrey, et al.
(författare)
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Stable carbon isotopes reveal soil - stream DIC linkages in contrasting headwater catchments
- 2018
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Ingår i: Journal of Geophysical Research - Biogeosciences. - : American Geophysical Union (AGU). - 2169-8953 .- 2169-8961. ; 123:1, s. 149-167
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Tidskriftsartikel (refereegranskat)abstract
- Large CO2 evasion to the atmosphere occurs as dissolved inorganic carbon (DIC) is transported from soils to streams. While this physical process has been the focus of multiple studies, less is known about the underlying biogeochemical transformations that accompany this transfer of C from soils to streams. Here we used patterns in stream water and groundwater C-13-DIC values within three headwater catchments with contrasting land cover to identify the sources and processes regulating DIC during its transport. We found that although considerable CO2 evasion occurs as DIC is transported from soils to streams, there were also other processes affecting the DIC pool. Methane production and mixing of C sources, associated with different types and spatial distribution of peat-rich areas within each catchment, had a significant influence on the C-13-DIC values in both soils and streams. These processes represent an additional control on C-13-DIC values and the catchment-scale cycling of DIC across different northern landscape types. The results from this study demonstrate that the transport of DIC from soils to streams results in more than just rapid CO2 evasion to the atmosphere but also represents a channel of C transformation, which questions some of our current conceptualizations of C cycling at the landscape scale. Plain Language Summary Large carbon dioxide emission to the atmosphere occurs as rainwater percolates through soils and into streams. This physical process is important for the global carbon cycle and has been the focus of multiple studies. However, less is known about the underlying processes that accompanies this transfer of carbon dioxide from soils to streams. Here we analyze the stable isotope composition of soil and stream carbon dioxide and demonstrate that methane production and mixing of carbon sources also occur in soils and streams. These processes were linked to different types and configurations of peat-rich areas, for example, bogs, fens, and riparian zones, found within each of the three studied catchments. Our results therefore demonstrate that the export of carbon dioxide from soils to streams not only results in emissions to the atmosphere but also represents a channel of transformation. This questions some of our current conceptualization of the catchment-scale cycling of carbon dioxide.
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| 7. |
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| 8. |
- Bolou-Bi, Bolou Emile, et al.
(författare)
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Use of stable Mg isotope ratios in identifying the base cation sources of stream water in the boreal Krycklan catchment (Sweden)
- 2022
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Ingår i: Chemical Geology. - : Elsevier. - 0009-2541 .- 1872-6836. ; 588
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Tidskriftsartikel (refereegranskat)abstract
- The knowledge of the sources of base cations in stream water is a prerequisite to assess potential effects of changing environmental conditions such as changing rainfall, weathering or groundwater flows on cation export with stream water. This study use stable Mg isotopes to identify potential sources in the well-studied catchment of Krycklan located on gneissic bedrock covered by quaternary sediments in Sweden. Samples were collected from open filed rain, throughfall, stream, soil, rock and litterfall. The delta Mg-26 values of these samples was determined and the contributions of different sources to Mg fluxes in the stream were determined from the variation of the Mg isotope and Sr / Mg ratios. The results show an overall variation of 1.10 parts per thousand between all samples. In addition, Magnesium isotope ratios varied little in the streamwater and in soil solution, except during snowmelt periods during which a large portion of the annual runoff occurs. Magnesium in the streamwater is explained as a mixture of three pools (open field rain, soil solution and groundwater) with the latter two influenced by catchment processes. Outside the snow-melt period, Mg in streamwater mainly derived from the groundwater, assumed to be mineral weathering signature in this catchment, with a contribution ranging from 12 to 63% to Mg fluxes. Open field rain dominates Mg fluxes in streamwater during spring flood (0 to 78%) and may contribute significantly during larger summer and autumn rainfall events. Soil solution input to streamwater range from 16 to 59% of Mg fluxes in streamwater. Our results demonstrate that delta Mg-26 values together with Mg concentrations and Sr/Mg ratios can be used to constrain the Mg sources of stream water and quantify weathering release rates.
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| 9. |
- Kritzberg, Emma S., et al.
(författare)
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Browning of freshwaters : Consequences to ecosystem services, underlying drivers, and potential mitigation measures
- 2020
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Ingår i: Ambio: a Journal of the Human Environment. - : Springer Science and Business Media LLC. - 0044-7447 .- 1654-7209. ; 49:2, s. 375-390
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Forskningsöversikt (refereegranskat)abstract
- Browning of surface waters, as a result of increasing dissolved organic carbon and iron concentrations, is a widespread phenomenon with implications to the structure and function of aquatic ecosystems. In this article, we provide an overview of the consequences of browning in relation to ecosystem services, outline what the underlying drivers and mechanisms of browning are, and specifically focus on exploring potential mitigation measures to locally counteract browning. These topical concepts are discussed with a focus on Scandinavia, but are of relevance also to other regions. Browning is of environmental concern as it leads to, e.g., increasing costs and risks for drinking water production, and reduced fish production in lakes by limiting light penetration. While climate change, recovery from acidification, and land-use change are all likely factors contributing to the observed browning, managing the land use in the hydrologically connected parts of the landscape may be the most feasible way to counteract browning of natural waters.
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| 10. |
- Wallin, Marcus, 1979-, et al.
(författare)
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Carbon dioxide and methane emissions of Swedish low-order streams : a national estimate and lessons learnt from more than a decade of observations
- 2018
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Ingår i: Limnology and Oceanography Letters. - : John Wiley & Sons. - 2378-2242. ; 3:3, s. 156-167
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Tidskriftsartikel (refereegranskat)abstract
- Low-order streams are suggested to dominate the atmospheric CO2 source of all inland waters. Yet, many large-scale stream estimates suffer from methods not designed for gas emission determination and rarely include other greenhouse gases such as CH4. Here, we present a compilation of directly measured CO2 and CH4 concentration data from Swedish low-order streams (> 1600 observations across > 500 streams) covering large climatological and land-use gradients. These data were combined with an empirically derived gas transfer model and the characteristics of a ca. 400,000 km stream network covering the entire country. The total stream CO2 and CH4 emission corresponded to 2.7 Tg C yr(-1) (95% confidence interval: 2.0-3.7) of which the CH4 accounted for 0.7% (0.02 Tg C yr(-1)). The study highlights the importance of low-order streams, as well as the critical need to better represent variability in emissions and stream areal extent to constrain future stream C emission estimates.
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