| 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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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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| 3. |
- Campeau, Audrey
(författare)
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Carbon in Boreal Streams : Isotopic Tracing of Terrestrial Sources
- 2019
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The boreal biome comprises vast areas of coniferous forests, dotted with millions of peatlands. Plants harbouring these ecosystems fix CO2 from the atmosphere, which is later incorporated into the vegetation biomass and subsequently buried in soils. Over the course of millennia, this process has led to the formation of a large repository of organic C, currently stored in boreal soils. Streams draining this landscape are typically enriched with carbon dioxide (CO2), methane (CH4) and dissolved organic carbon (DOC). As a consequence, streams tend to emit CO2 and CH4 to the atmosphere, two potent greenhouse gases, and thus contribute positively to radiative climate forcing. The sources fuelling C to boreal streams are not well understood. This thesis aims to unravel these sources, and promote a better consolidation of terrestrial and aquatic C biogeochemical processes. The work is largely based on stable and radiogenic C isotope characterization of various dissolved C forms in stream and groundwater, within contrasting ecosystem types across Sweden.This thesis identifies boreal soils as the main source of CO2 in streams. Soil respiration (i.e. biogenic sources) overwhelmingly supply CO2 to streams, leaving only a few exceptions where geogenic CO2 sources were present. An array of biological processes also transform CO2 during its transport from soils to streams. These include; methanogenesis, aquatic DOC mineralization and primary production. The majority of C in boreal streams is sustained by the decomposition of recent photosynthates, with ancient C substrates holding a negligible share of the total C export. While these results suggest that the repository of ancient soil organic C is currently stable, within boreal forests and peatlands, the close connection with recently occurring photosynthesis suggest that forecasted alterations in plant C allocation patterns, driven by climate and land-use changes, will produce a rapid response in stream CO2 emissions. Isotopic characterization of C in stream and groundwater can help reveal these sources and transformation processes, but its interpretation must be made with care.
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| 4. |
- 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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| 5. |
- Campeau, Audrey, et al.
(författare)
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Multiple sources and sinks of dissolved inorganic carbon across Swedish streams, refocusing the lens of stable C isotopes
- 2017
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Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 7
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Tidskriftsartikel (refereegranskat)abstract
- It is well established that stream dissolved inorganic carbon (DIC) fluxes play a central role in the global C cycle, yet the sources of stream DIC remain to a large extent unresolved. Here, we explore large-scale patterns in delta C-13-DIC from streams across Sweden to separate and further quantify the sources and sinks of stream DIC. We found that stream DIC is governed by a variety of sources and sinks including biogenic and geogenic sources, CO2 evasion, as well as in-stream processes. Although soil respiration was the main source of DIC across all streams, a geogenic DIC influence was identified in the northernmost region. All streams were affected by various degrees of atmospheric CO2 evasion, but residual variance in delta C-13-DIC also indicated a significant influence of in-stream metabolism and anaerobic processes. Due to those multiple sources and sinks, we emphasize that simply quantifying aquatic DIC fluxes will not be sufficient to characterise their role in the global C cycle.
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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. |
- Riml, Joakim, 1979-, et al.
(författare)
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Spectral Decomposition Reveals New Perspectives on CO2 Concentration Patterns and Soil-Stream Linkages
- 2019
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Ingår i: Journal of Geophysical Research - Biogeosciences. - : American Geophysical Union (AGU). - 2169-8953 .- 2169-8961. ; 124:10, s. 3039-3056
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Tidskriftsartikel (refereegranskat)abstract
- The rapid development of novel technologies to obtain high-frequency observations has provided new possibilities to observe and understand carbon cycling in inland waters. This study investigates carbon dioxide (CO2) dynamics along a boreal soil-stream transect using a state-of-the-art data set in combination with a spectral methodology to identify controls on stream CO2. The spectral decomposition of hourly observations revealed intermediate (multiday) to long-term (monthly) patterns across the upslope-riparian-stream continuum, with similar power law increases in CO2 concentration fluctuations with increasing period. High-frequency CO2 variabilities, specifically diel CO2 concentration fluctuations, were also identified at all locations but were substantially amplified in the stream compared to in the riparian groundwater. Moreover, the spectral coherence between soil and stream CO2 fluctuations was inconsistent and restricted to episodic events. In contrast, we found a strong and consistent spectral coherence between the riparian groundwater level and stream CO2 concentration, indicating a hydrological control on stream CO2 dynamics. However, during some time spans even these patterns were obscured, suggesting that additional processes, such as CO2 evasion and in-stream metabolism, modulated the influence from riparian sources. The scales and patterns of temporal coherences (or lack thereof) between CO2 at different points in the catchment, as well as with other factors, for example, groundwater levels and Photosynthetically Active Radiation, provide new perspectives on the range of processes governing stream CO2 dynamics. Thus, this study highlights the potential of using spectral decomposition of high-resolution, spatially distributed data of different types to investigate biogeochemical transformations and pathways linking terrestrial and aquatic systems.
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| 8. |
- 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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