| 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±1.8µgN/L, respectively (mean±SD) despite higher total N (TN) concentrations in agricultural streams (1,520±1,640 vs. 780±600µgN/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 ~1.8×109g 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 800×109gCO2-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. |
- Abbott, Benjamin, et al.
(författare)
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Using multi-tracer inference to move beyond single-catchment ecohydrology
- 2016
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Ingår i: Earth-Science Reviews. - : Elsevier BV. - 0012-8252 .- 1872-6828. ; 160, s. 19-42
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Tidskriftsartikel (refereegranskat)abstract
- Protecting or restoring aquatic ecosystems in the face of growing anthropogenic pressures requires an understanding of hydrological and biogeochemical functioning across multiple spatial and temporal scales. Recent technological and methodological advances have vastly increased the number and diversity of hydrological, biogeochemical, and ecological tracers available, providing potentially powerful tools to improve understanding of fundamental problems in ecohydrology, notably: 1. Identifying spatially explicit flowpaths, 2. Quantifying water residence time, and 3. Quantifying and localizing biogeochemical transformation. In this review, we synthesize the history of hydrological and biogeochemical theory, summarize modem tracer methods, and discuss how improved understanding of flowpath, residence time, and biogeochemical transformation can help ecohydrology move beyond description of site-specific heterogeneity. We focus on using multiple tracers with contrasting characteristics (crossing proxies) to infer ecosystem functioning across multiple scales. Specifically, we present how crossed proxies could test recent ecohydrological theory, combining the concepts of hotspots and hot moments with the Damkohler number in what we call the HotDam framework.
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| 3. |
- Audet, Joachim, et al.
(författare)
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Nitrous oxide emissions from streams in a Swedish agricultural catchment
- 2017
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Ingår i: Agriculture, Ecosystems & Environment. - : Elsevier BV. - 0167-8809 .- 1873-2305. ; 236, s. 295-303
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Tidskriftsartikel (refereegranskat)abstract
- Excess nitrogen fertiliser in agricultural soils might be leached to streams and converted to the greenhouse gas nitrous oxide (N2O). To assess the importance of N2O emissions from agricultural streams, concentration dynamics and emissions N2O emissions in streams were investigated in a 32 km2 lowland agricultural catchment located in Sweden. Dissolved N2O concentration was measured at nine occasions between December 2014 and August 2015 at nine stream stations. The stream stations represented sub-catchments with different land use characteristics with agricultural land use ranging from 0 to 63% of the area. Stream N2O percentage saturation ranged 40-2701% and showed large spatial and temporal variations. Statistical analysis using mixed models revealed that N2O concentration was significantly linked to nitrate concentration in the stream water, to the percentage arable land in the sub catchments as well as to the stream water discharge. Using two empirical equations to estimate the N2O emissions showed that streams were generally a source of N2O to the atmosphere (mean 108 and 175 mu g N m(-2) h(-1) with first and second equation). The catchment scale estimate of N2O stream emissions was compared to the estimate obtained using IPCC guidelines linking N fertilisation inputs and leaching to N2O emissions. The comparison suggested that N2O stream emission calculated using the IPCC methodology might be underestimated. A coarse estimate suggests that N2O stream emissions represent about 4% of the total N2O emissions from N-fertiliser at the catchment scale. Hence while streams covered only 0.1% of the catchment area they were of disproportionate importance as a source of N2O to the atmosphere.
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| 4. |
- 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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| 5. |
- 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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| 6. |
- 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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| 7. |
- 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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| 8. |
- 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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| 9. |
- Dinsmore, Kerry, et al.
(författare)
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Contrasting CO2 concentration discharge dynamics in headwater streams : a multi-catchment comparison
- 2013
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Ingår i: Journal of Geophysical Research-Biogeosciences. - : American Geophysical Union (AGU). - 2169-8953 .- 2169-8961. ; 118:2, s. 445-461
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Tidskriftsartikel (refereegranskat)abstract
- Aquatic CO2 concentrations are highly variable and strongly linked to discharge, but until recently, measurements have been largely restricted to low-frequency manual sampling. Using new in situ CO2 sensors, we present concurrent, high-frequency (<30 min resolution) CO2 concentration and discharge data collected from five catchments across Canada, UK, and Fennoscandinavia to explore concentration-discharge dynamics; we also consider the relative importance of high flows to lateral aquatic CO2 export. The catchments encompassed a wide range of mean CO2 concentrations (0.73–3.05 mg C L−1) and hydrological flow regimes from flashy peatland streams to muted outflows within a Finnish lake system. In three of the catchments, CO2 concentrations displayed clear bimodal distributions indicating distinct CO2 sources. Concentration-discharge relationships were not consistent across sites with three of the catchments displaying a negative relationship and two catchments displaying a positive relationship. When individual high flow events were considered, we found a strong correlation between both the average magnitude of the hydrological and CO2 response peaks, and the average response lag times. An analysis of lateral CO2 export showed that in three of the catchments, the top 30% of flow (i.e., flow that was exceeded only 30% of the time) had the greatest influence on total annual load. This indicates that an increase in precipitation extremes (greater high-flow contributions) may have a greater influence on the flushing of CO2 from soils to surface waters than a long-term increase in mean annual precipitation, assuming source limitation does not occur.
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| 10. |
- Guseva, S., et al.
(författare)
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Variable Physical Drivers of Near-Surface Turbulence in a Regulated River
- 2021
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Ingår i: Water resources research. - : American Geophysical Union (AGU). - 0043-1397 .- 1944-7973. ; 57:11
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Tidskriftsartikel (refereegranskat)abstract
- Inland waters, such as lakes, reservoirs and rivers, are important sources of climate forcing trace gases. A key parameter that regulates the gas exchange between water and the atmosphere is the gas transfer velocity, which itself is controlled by near-surface turbulence in the water. While in lakes and reservoirs, near-surface turbulence is mainly driven by atmospheric forcing, in shallow rivers and streams it is generated by bottom friction of gravity-forced flow. Large rivers represent a transition between these two cases. Near-surface turbulence has rarely been measured in rivers and the drivers of turbulence have not been quantified. We analyzed continuous measurements of flow velocity and quantified turbulence as the rate of dissipation of turbulent kinetic energy over the ice-free season in a large regulated river in Northern Finland. Measured dissipation rates agreed with predictions from bulk parameters, including mean flow velocity, wind speed, surface heat flux, and with a one-dimensional numerical turbulence model. Values ranged from to . Atmospheric forcing or gravity was the dominant driver of near-surface turbulence for similar fraction of the time. Large variability in near-surface dissipation rate occurred at diel time scales, when the flow velocity was strongly affected by downstream dam operation. By combining scaling relations for boundary-layer turbulence at the river bed and at the air-water interface, we derived a simple model for estimating the relative contributions of wind speed and bottom friction of river flow as a function of depth.Plain Language SummaryInland water bodies such as lakes, reservoirs and rivers are an important source of climate forcing trace gases to the atmosphere. Gas exchange between water and the atmosphere is regulated by the gas transfer velocity and the concentration difference between the water surface and the atmosphere. The gas transfer velocity depends on near-surface turbulence, but robust formulations have not been developed for river systems. Their surface area is sufficiently large for meteorological forcing to cause turbulence, as in lakes and reservoirs, but turbulence generated from bed and internal friction of gravity-driven flows is also expected to contribute. Here we quantify near-surface turbulence using data from continuous air and water side measurements conducted over the ice-free season in a large subarctic regulated river in Finland. We find that turbulence, quantified as the dissipation rate of turbulent kinetic energy, is well described using equations for predicting turbulence from meteorological data for sufficiently high wind speeds whereas the contribution from bottom shear dominated at higher flow velocities. A one-dimensional river model successfully captured these processes. We provide a fundamental model for estimating the relative contributions of atmospheric forcing and bottom friction as a function of depth.
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