| 1. |
- Campeau, Audrey, et al.
(författare)
-
Aquatic export of young dissolved and gaseous carbon from a pristine boreal fen : Implications for peat carbon stock stability
- 2017
-
Ingår i: Global Change Biology. - : Wiley. - 1354-1013 .- 1365-2486. ; 23:12, s. 5523-5536
-
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.
|
|
| 2. |
- Campeau, Audrey, et al.
(författare)
-
Current forest carbon fixation fuels stream CO 2 emissions
- 2019
-
Ingår i: Nature Communications. - : Nature Publishing Group. - 2041-1723. ; 10:1
-
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).
|
|
| 3. |
- Campeau, Audrey, et al.
(författare)
-
Stable carbon isotopes reveal soil - stream DIC linkages in contrasting headwater catchments
- 2018
-
Ingår i: Journal of Geophysical Research - Biogeosciences. - : American Geophysical Union (AGU). - 2169-8953 .- 2169-8961. ; 123:1, s. 149-167
-
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.
|
|
| 4. |
- Haei, Mahsa, 1981-, et al.
(författare)
-
Cold winter soils enhance dissolved organic carbon concentrations in soil and stream water
- 2010
-
Ingår i: Geophysical Research Letters. - : American Geophysical Union. - 0094-8276 .- 1944-8007. ; 37, s. L08501-
-
Tidskriftsartikel (refereegranskat)abstract
- Concentrations of dissolved organic carbon ([DOC]) have increased in lakes, streams and rivers across a large part of the northern hemisphere and raised an animated scientific debate about the underlying mechanisms. The lack of consensus about the role of climate in controlling the DOC trends highlights the need for understanding the regulation of surface water DOC. We found that longer and colder winters result in higher [DOC] in a boreal headwater stream during the subsequent snowmelt. In addition, prolonged soil frost increases the spring and summer [DOC] in the riparian soil water, which is a major contributor of stream water DOC in the studied area. We conclude that winter climatic conditions can play a substantial role in controlling stream [DOC] in ways not previously understood. These findings are especially important for northern latitude regions expected to be most affected by climate change. Citation: Haei, M., M. G. Oquist, I. Buffam, A. angstrom gren, P. Blomkvist, K. Bishop, M. Ottosson Lofvenius, and H. Laudon (2010), Cold winter soils enhance dissolved organic carbon concentrations in soil and st ream water, Geophys. Res. Lett., 37, L08501, doi: 10.1029/2010GL042821.
|
|
| 5. |
- Noumonvi, Koffi Dodji, et al.
(författare)
-
The Kulbäcksliden research infrastructure : a unique setting for northern peatland studies
- 2023
-
Ingår i: Frontiers in Earth Science. - : Frontiers Media S.A.. - 2296-6463. ; 11
-
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.
|
|
| 6. |
- Smeds, Jacob, et al.
(författare)
-
A Simplified Drying Procedure for Analysing Hg Concentrations
- 2022
-
Ingår i: Water, Air, and Soil Pollution. - : Springer Science and Business Media LLC. - 0049-6979 .- 1573-2932. ; 233
-
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.
|
|
| 7. |
- Wallin, Marcus B., et al.
(författare)
-
Spatiotemporal variability of the gas transfer coefficient (KCO2) in boreal streams : Implications for large scale estimates of CO2 evasion
- 2011
-
Ingår i: Global Biogeochemical Cycles. - : John Wiley & Sons. - 0886-6236 .- 1944-9224. ; 25:3, s. GB3025-
-
Tidskriftsartikel (refereegranskat)abstract
- Boreal streams represent potentially important conduits for the exchange of carbon dioxide (CO(2)) between terrestrial ecosystems and the atmosphere. The gas transfer coefficient of CO(2) (K(CO2)) is a key variable in estimating this source strength, but the scarcity of measured values in lotic systems creates a risk of incorrect flux estimates even when stream gas concentrations are well known. This study used 114 independent measurements of K(CO2) from 14 stream reaches in a boreal headwater system to determine and predict spatiotemporal variability in K(CO2). The K(CO2) values ranged from 0.001 to 0.207 min(-1) across the 14 sites. Median K(CO2) for a specific site was positively correlated with the slope of the stream reach, with higher gas transfer coefficients occurring in steeper stream sections. Combining slope with a width/depth index of the stream reach explained 83% of the spatial variability in K(CO2). Temporal variability was more difficult to predict and was strongly site specific. Variation in K(CO2), rather than pCO(2), was the main determinant of stream CO(2) evasion. Applying published generalized gas transfer velocities produced an error of up to 100% in median instantaneous evasion rates compared to the use of actual measured K(CO2) values from our field study. Using the significant relationship to local slope, the median K(CO2) was predicted for 300,000 km of watercourses (ranging in stream order 1-4) in the forested landscape of boreal/nemoral Sweden. The range in modeled stream order specific median K(CO2) was 0.017-0.028 min(-1) and there was a clear gradient of increasing K(CO2) with lower stream order. We conclude that accurate regional scale estimates of CO(2) evasion fluxes from running waters are possible, but require a good understanding of gas exchange at the water surface.
|
|
| 8. |
- Wallin, Marcus, et al.
(författare)
-
Evasion of CO2 from streams : The dominant component of the carbon export through the aquatic conduit in a boreal landscape
- 2013
-
Ingår i: Global Change Biology. - : Wiley. - 1354-1013 .- 1365-2486. ; 19:3, s. 785-797
-
Tidskriftsartikel (refereegranskat)abstract
- Evasion of gaseous carbon (C) from streams is often poorly quantified in landscape C budgets. Even though the potential importance of the capillary network of streams as C conduits across the land-water-atmosphere interfaces is sometimes mentioned, low-order streams are often left out of budget estimates due to being poorly characterized in terms of gas exchange and even areal surface coverage. We show that evasion of C is greater than all the total dissolved C (both organic and inorganic) exported downstream in the waters of a boreal landscape. In this study evasion of carbon dioxide (CO2) from running waters within a 67 km2 boreal catchment was studied. During a four year period (2006-2009) 13 streams were sampled on 104 different occasions for dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC). From a locally determined model of gas exchange properties, we estimated the daily CO2 evasion with a high-resolution (5×5 m) grid based stream evasion model comprising the entire ~100 km stream network. Despite the low areal coverage of stream surface the evasion of CO2 from the stream network constituted 53% (5.0 (±1.8) g C m−2 yr−1) of the entire stream C flux (9.6 (±2.4) g C m−2 yr−1) (lateral as DIC, DOC and vertical as CO2). In addition, 72% of the total CO2 loss took place already in the 1st and 2nd order streams. This study demonstrates the importance of including CO2 evasion from low-order boreal streams into landscape C budgets since it more than doubled the magnitude of the aquatic conduit for C from this landscape. Neglecting this term will consequently result in an overestimation of the terrestrial C sink strength in the boreal landscape.
|
|
| 9. |
- Wallin, Marcus, et al.
(författare)
-
Temporal and spatial variability of dissolved inorganic carbon in a boreal stream network: Concentrations and downstream fluxes
- 2010
-
Ingår i: Journal of Geophysical Research: Biogeosciences. - 2169-8953 .- 2169-8961. ; 115, s. G02014-
-
Tidskriftsartikel (refereegranskat)abstract
- Carbon dioxide (CO(2)) and dissolved inorganic carbon (DIC) concentrations and export were analyzed throughout a 67 km(2) boreal stream network in northern Sweden. 700 DIC and CO(2) samples from 14 subcatchments were collected in 2006 and 2007. All sites were consistently supersaturated in CO(2) with respect to the atmosphere. Temporal variability of DIC and CO(2) concentration was best correlated with discharge, with concentrations generally diluting at high discharge. However, the variability in CO(2) concentration was also dependent on the specific pH range of the stream, as variability was greatest in acidic headwater streams and lowest in larger circumneutral streams. In the larger ones the increase in the CO(2) proportion of DIC at increased discharge counteracts the dilution of CO(2). The shift toward proportionally more CO(2) of the DIC at higher discharge is caused by decline in pH. Spatial patterns showed that DIC and CO(2) concentrations were best correlated with peatland coverage of the subcatchment. The highest concentrations were found in headwater streams draining peatlands. The downstream export of DIC from the catchment outlet constitutes 19% of the total downstream export of carbon (DIC + DOC), or 0.7 (+/-0.09) g C m(-2) yr(-1). This study demonstrates the importance of including fluvial fluxes of inorganic carbon in landscape carbon budgets via runoff, and also highlights the need to account for stream evasion of CO(2) to the atmosphere in such estimates since it can be larger than the downstream DIC export.
|
|
| 10. |
- Öquist, Mats, et al.
(författare)
-
Dissolved Inorganic Carbon Export Across the Soil/Stream Interface and Its Fate in a Boreal Headwater Stream
- 2009
-
Ingår i: Environmental Science & Technology. - : American Chemical Society (ACS). ; 43, s. 7364-7369
-
Tidskriftsartikel (refereegranskat)abstract
- The aim of this investigation was to determine the lateral export of dissolved inorganic carbon (DIC) from soils of a Swedish boreal forest to a first order stream and to estimate the partitioning of this DIC into CO2 evasion from the stream surface and the DIC pool exported down through the catchment by streamwater. The groundwater entering the stream was supersaturated with CO2 with values as high as 17 times equilibrium with the atmosphere. Up to 90% of the estimated daily soil DIC export to the stream was emitted to the atmosphere as CO2 within 200 in of the water entering the stream. The annual DIC export from the soil to the stream was estimated to be 3.2 (+/- 0.1) g C m(-2) yr(-1) (normalized to catchment size). Ninety percent of the variation in soil DIC export could be explained by the variation in groundwater discharge and the DIC concentrations per se, were of minor importance. A significant correlation (R-2 = 0.74, P < 0.01) between soil DIC export and CO2 emission from the stream surface suggests that emission dynamics were primarily driven by the export of terrestrial DIC and that in-stream processes were less important Our results reveal that current budget estimates of lateral DIC export from soils to aquatic conduits need to be revised because they do not account for conditions prevailing in headwater streams. Any quantification of lateral stream C export and CO2 emissions from freshwater systems must include headwater streams as well as the lower parts of the aquatic conduit
|
|
