| 1. |
- Campeau, Audrey, et al.
(författare)
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Aquatic export of young dissolved and gaseous carbon from a pristine boreal fen : Implications for peat carbon stock stability
- 2017
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Ingår i: Global Change Biology. - : Wiley. - 1354-1013 .- 1365-2486. ; 23:12, s. 5523-5536
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Tidskriftsartikel (refereegranskat)abstract
- The stability of northern peatland's carbon (C) store under changing climate is of major concern for the global C cycle. The aquatic export of C from boreal peatlands is recognized as both a critical pathway for the remobilization of peat C stocks as well as a major component of the net ecosystem C balance (NECB). Here, we present a full year characterization of radiocarbon content (14C) of dissolved organic carbon (DOC), carbon dioxide (CO2), and methane (CH4) exported from a boreal peatland catchment coupled with 14C characterization of the catchment's peat profile of the same C species. The age of aquatic C in runoff varied little throughout the year and appeared to be sustained by recently fixed C from the atmosphere (<60 years), despite stream DOC, CO2, and CH4 primarily being sourced from deep peat horizons (2–4 m) near the mire's outlet. In fact, the 14C content of DOC, CO2, and CH4 across the entire peat profile was considerably enriched with postbomb C compared with the solid peat material. Overall, our results demonstrate little to no mobilization of ancient C stocks from this boreal peatland and a relatively large resilience of the source of aquatic C export to forecasted hydroclimatic changes.
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| 2. |
- 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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| 3. |
- Noumonvi, Koffi Dodji, et al.
(författare)
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The Kulbäcksliden research infrastructure : a unique setting for northern peatland studies
- 2023
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Ingår i: Frontiers in Earth Science. - : Frontiers Media S.A.. - 2296-6463. ; 11
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Forskningsöversikt (refereegranskat)abstract
- Boreal peatlands represent a biogeochemically unique and diverse environment in high-latitude landscape. They represent a long-term globally significant sink for carbon dioxide and a source of methane, hence playing an important role in regulating the global climate. There is an increasing interest in deciphering peatland biogeochemical processes to improve our understanding of how anthropogenic and climate change effects regulate the peatland biogeochemistry and greenhouse gas balances. At present, most studies investigating land-atmosphere exchanges of peatland ecosystems are commonly based on single-tower setups, which require the assumption of homogeneous conditions during upscaling to the landscape. However, the spatial organization of peatland complexes might feature large heterogeneity due to its varying underlying topography and vegetation composition. Little is known about how well single site studies represent the spatial variations of biogeochemical processes across entire peatland complexes. The recently established Kulbäcksliden Research Infrastructure (KRI) includes five peatland study sites located less than 3 km apart, thus providing a unique opportunity to explore the spatial variation in ecosystem-scale processes across a typical boreal peatland complex. All KRI sites are equipped with eddy covariance flux towers combined with installations for detailed monitoring of biotic and abiotic variables, as well as catchment-scale hydrology and hydrochemistry. Here, we review studies that were conducted in the Kulbäcksliden area and provide a description of the site characteristics as well as the instrumentation available at the KRI. We highlight the value of long-term infrastructures with ecosystem-scale and replicated experimental sites to advance our understanding of peatland biogeochemistry, hydrology, ecology, and its feedbacks on the environment and climate system.
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| 4. |
- Osterwalder, S., et al.
(författare)
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Critical Observations of Gaseous Elemental Mercury Air-Sea Exchange
- 2021
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Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 35:8
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Tidskriftsartikel (refereegranskat)abstract
- Air-sea exchange of gaseous elemental mercury (Hg-0) is not well constrained, even though it is a major component of the global Hg cycle. Lack of Hg-0 flux measurements to validate parameterizations of the Hg-0 transfer velocity contributes to this uncertainty. We measured the Hg-0 flux on the Baltic Sea coast using micrometeorological methods (gradient-based and relaxed eddy accumulation [REA]) and also simulated the flux with a gas exchange model. The coastal waters were typically supersaturated with Hg-0 (mean +/- 1 sigma = 13.5 +/- 3.5 ng m(-3); ca. 10% of total Hg) compared to the atmosphere (1.3 +/- 0.2 ng m(-3)). The Hg-0 flux calculated using the gas exchange model ranged from 0.1-1.3 ng m(-2) h(-1) (10th and 90th percentile) over the course of the campaign (May 10-June 20, 2017) and showed a distinct diel fluctuation. The mean coastal Hg-0 fluxes determined with the two gradient-based approaches and REA were 0.3, 0.5, and 0.6 ng m(-2) h(-1), respectively. In contrast, the mean open sea Hg-0 flux measured with REA was larger (6.3 ng m(-2) h(-1)). The open sea Hg-0 flux indicated a stronger wind speed dependence for the Hg-0 transfer velocity compared to commonly used parameterizations. Although based on a limited data set, we suggest that the wind speed dependence of the Hg-0 transfer velocity is more consistent with gases that have less water solubility than CO2 (e.g., O-2). These pioneering flux measurements using micrometeorological techniques show that more such measurements would improve our understanding of air-sea Hg exchange.
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| 5. |
- Smeds, Jacob, et al.
(författare)
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A Simplified Drying Procedure for Analysing Hg Concentrations
- 2022
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Ingår i: Water, Air, and Soil Pollution. - : Springer Science and Business Media LLC. - 0049-6979 .- 1573-2932. ; 233
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Tidskriftsartikel (refereegranskat)abstract
- Mercury (Hg) in peatlands remains a problem of global interest. To mitigate the risks of this neurotoxin, accurate assessments of Hg in peat are needed. Treatment of peat that will be analysed for Hg is, however, not straightforward due to the volatile nature of Hg. The drying process is of particular concern since Hg evasion increases with the temperature. Samples are, therefore, often freeze-dried to limit Hg loss during the drying processes. A problem with freeze-drying is that cost and equipment resources can limit the number of samples analysed in large projects. To avoid this bottleneck, we tested if drying in a 60 degrees C-degree oven could be an acceptable alternative to freeze-drying. We both freeze-dried and oven-dried (60 degrees C) 203 replicate pairs of peat samples, and then examined the differences in total Hg concentration. The Hg concentration differed significantly between the two drying methods with a median Hg deficit in oven-dried samples of 4.2%. Whether a 4.2% deficit of Hg depends on one's purpose. The lower median Hg concentration in oven-dried samples has to be weighed against the upside efficiently drying large sets of peat samples. By freeze-drying a subset of the samples, we fitted a function to correct for Hg loss during oven-drying (y = 0.96x + 0.08). By applying this correction, the freeze-drying bottleneck could oven-dry large-scale inventories of total Hg in peatlands with results equivalent to freeze-drying, but only have to freeze-dry a subset.
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| 6. |
- Öquist, Mats, et al.
(författare)
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The full annual carbon balance of boreal forestsis highly sensitive to precipitation
- 2014
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Ingår i: Environmental Science and Technology Letters. - : American Chemical Society (ACS). - 2328-8930. ; 1:7, s. 315-319
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Tidskriftsartikel (refereegranskat)abstract
- The boreal forest carbon balance is predicted to be particularly sensitive to climate change. Carbon balance estimates of these biomes stem mainly from eddy-covariance measurements of net ecosystem exchange (NEE). However, a full net ecosystem carbon balance (NECB) must include the lateral carbon export (LCE) through discharge. We show that annual LCE at a boreal forest site ranged from 4 to 28%, averaging 11% (standard deviation of 8%), of annual NEE over 13 years. Annual LCE and NEE are strongly anticorrelated; years with weak NEE coincide with high LCE. The decreased NEE in response to increased precipitation is caused by a reduction in the amount of incoming radiation caused by clouds. If our finding is also valid for other sites, it implies that increased precipitation at high latitudes may shift forest NECB in large areas of the boreal biome. Our results call for future analysis of this dual effect of precipitation on NEE and LCE.
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| 7. |
- Bergman, Inger, et al.
(författare)
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The influence of sulphate deposition on the seasonal variation of peat pore water methyl Hg in a boreal mire
- 2012
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Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 7:9, s. e45547-
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Tidskriftsartikel (refereegranskat)abstract
- In this paper we investigate the hypothesis that long-term sulphate (SO42-) deposition has made peatlands a larger source of methyl mercury (MeHg) to remote boreal lakes. This was done on experimental plots at a boreal, low sedge mire where the effect of long-term addition of SO42- on peat pore water MeHg concentrations was observed weekly throughout the snow-free portion of 1999. The additions of SO42- started in 1995. The seasonal mean of the pore water MeHg concentrations on the plots with 17 kg ha(-1) yr(-1) of sulphur (S) addition (1.3 +/- 0.08 ng L-1, SE; n=44) was significantly (p<0.0001) higher than the mean MeHg concentration on the plots with 3 kg ha(-1) yr(-1) of ambient S deposition (0.6 +/- 0.02 ng L-1, SE; n=44). The temporal variation in pore water MeHg concentrations during the snow free season was larger in the S-addition plots, with an amplitude of >2 ng L-1 compared to +/-0.5 ng L-1 in the ambient S deposition plots. The concentrations of pore water MeHg in the S-addition plots were positively correlated (r(2)=0.21; p=0.001) to the groundwater level, with the lowest concentrations of MeHg during the period with the lowest groundwater levels. The pore water MeHg concentrations were not correlated to total Hg, DOC concentration or pH. The results from this study indicate that the persistently higher pore water concentrations of MeHg in the S-addition plots are caused by the long-term additions of SO42- to the mire surface. Since these waters are an important source of runoff, the results support the hypothesis that SO42- deposition has increased the contribution of peatlands to MeHg in downstream aquatic systems. This would mean that the increased deposition of SO42- in acid rain has contributed to the modern increase in the MeHg burdens of remote lakes hydrologically connected to peatlands.
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| 8. |
- Bishop, Kevin, et al.
(författare)
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The Effects of Forestry on Hg Bioaccumulation in Nemoral/Boreal Waters and Recommendations for Good Silvicultural Practice
- 2009
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Ingår i: Ambio. - : Royal Swedish Academy of Sciences. - 0044-7447 .- 1654-7209. ; 38:7, s. 373-380
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Tidskriftsartikel (refereegranskat)abstract
- Mercury (Hg) levels are alarmingly high in fish from lakes across Fennoscandia and northern North America. The few published studies on the ways in which silviculture practices influence this problem indicate that forest operations increase Hg in downstream aquatic ecosystems. From these studies, we estimate that between one-tenth and one-quarter of the Hg in the fish of high-latitude, managed forest landscapes can be attributed to harvesting. Forestry, however, did not create the elevated Hg levels in the soils, and waterborne Hg/MeHg concentrations downstream from harvested areas are similar to those from wetlands. Given the current understanding of the way in which silviculture impacts Hg cycling, most of the recommendations for good forest practice in Sweden appear to be appropriate for high-latitude regions, e.g., leaving riparian buffer zones, as well as reducing disturbance at stream crossings and in moist areas. The recommendation to restore wetlands and reduce drainage, however, will likely increase Hg/MeHg loadings to aquatic ecosystems
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| 9. |
- Campeau, Audrey, et al.
(författare)
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Autumn destabilization of deep porewater CO2 store in a northern peatland driven by turbulent diffusion
- 2021
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Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 12:1
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Tidskriftsartikel (refereegranskat)abstract
- The deep porewater of northern peatlands stores large amounts of carbon dioxide (CO2). This store is viewed as a stable feature in the peatland CO2 cycle. Here, we report large and rapid fluctuations in deep porewater CO2 concentration recurring every autumn over four consecutive years in a boreal peatland. Estimates of the vertical diffusion of heat indicate that CO2 diffusion occurs at the turbulent rather than molecular rate. The weakening of porewater thermal stratification in autumn likely increases turbulent diffusion, thus fostering a rapid diffusion of deeper porewater CO2 towards the surface where net losses occur. This phenomenon periodically decreases the peat porewater CO2 store by between 29 and 90 g C m−2 throughout autumn, which is comparable to the peatland’s annual C-sink. Our results establish the need to consider the role of turbulent diffusion in regularly destabilizing the CO2 store in peat porewater.
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| 10. |
- Fritsche, Johannes, et al.
(författare)
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Evasion of Elemental Mercury from a Boreal Peat land Suppressed by Long-Term Sulfate Addition
- 2014
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Ingår i: ENVIRONMENTAL SCIENCE & TECHNOLOGY LETTERS. - : American Chemical Society (ACS). - 2328-8930. ; 1:10, s. 421-425
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Tidskriftsartikel (refereegranskat)abstract
- We investigated the evasion of TGM (total gaseous mercury) from experimental plots on a boreal peatland that had been exposed for 15 years to different combinations of atmospheric sulfur (5) and nitrogen (N) deposition as well as greenhouse treatments simulating climate change. Shaded dynamic flux chamber measurements during the summer in 2009 showed emission of TGM to the atmosphere from most of the treated plots (0.7 +/- 0.94 ng m(-2) h(-1)). However, TGM exchange rates were significantly lower, occasionally indicating Hg uptake, on plots subjected to S addition at rates of 20 kg ha(-1) year(-1). Enhanced nitrogen deposition and greenhouse treatment had no significant effect on TGM fluxes. We hypothesize that the lower Hg evasion from the sulfur-treated plots is related to either earlier Hg evasion or Hg binding to S in organic matter, making, Hg less susceptible to volatilization and more prone to transport in runoff.
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