| 1. |
- Audet, J., et al.
(författare)
-
Forest streams are important sources for nitrous oxide emissions
- 2020
-
Ingår i: Global Change Biology. - : Wiley. - 1354-1013 .- 1365-2486. ; 26:2, s. 629-641
-
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 µg N/L, respectively (mean ± SD) despite higher total N (TN) concentrations in agricultural streams (1,520 ± 1,640 vs. 780 ± 600 µg 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 × 109 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 × 109 g CO2-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
|
|
| 2. |
- Audet, Joachim, et al.
(författare)
-
Nitrous oxide emissions from streams in a Swedish agricultural catchment
- 2017
-
Ingår i: Agriculture, Ecosystems & Environment. - : Elsevier BV. - 0167-8809 .- 1873-2305. ; 236, s. 295-303
-
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.
|
|
| 3. |
- Campeau, Audrey, et al.
(författare)
-
Autumn destabilization of deep porewater CO2 store in a northern peatland driven by turbulent diffusion
- 2021
-
Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 12:1
-
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.
|
|
| 4. |
- Guseva, S., et al.
(författare)
-
Variable Physical Drivers of Near-Surface Turbulence in a Regulated River
- 2021
-
Ingår i: Water resources research. - : American Geophysical Union (AGU). - 0043-1397 .- 1944-7973. ; 57:11
-
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.
|
|
| 5. |
- Gutiérrez Loza, Lucia, et al.
(författare)
-
On physical mechanisms enhancing air-sea CO2 exchange
- 2022
-
Ingår i: Biogeosciences. - : European Geosciences Union (EGU). - 1726-4170 .- 1726-4189. ; 19:24, s. 5645-5665
-
Tidskriftsartikel (refereegranskat)abstract
- Reducing uncertainties in the air–sea CO2 flux calculations is one of the major challenges when addressing the oceanic contribution in the global carbon balance. In traditional models, the air–sea CO2 flux is estimated using expressions of the gas transfer velocity as a function of wind speed. However, other mechanisms affecting the variability in the flux at local and regional scales are still poorly understood. The uncertainties associated with the flux estimates become particularly large in heterogeneous environments such as coastal and marginal seas. Here, we investigated the air–sea CO2 exchange at a coastal site in the central Baltic Sea using nine years of eddy covariance measurements. Based on these observations we were able to capture the temporal variability of the air–sea CO2 flux and other parameters relevant for the gas exchange. Our results show that a wind-based model with similar pattern to those developed for larger basins and open sea condition can, on average, be a good approximation for k. However, in order to reduce the uncertainty associated to these averages and produce reliable short-term k estimates, additional physical processes must be considered. Using a normalized gas transfer velocity, we identified conditions associated to enhanced exchange (large k values). During high and intermediate wind speeds (above 6–8 m s−1),conditions on both sides of the air–water interface were found to be relevant for the gas exchange. Our findings further suggest that at such relatively high wind speeds, sea spray is an efficient mechanisms for air–sea CO2 exchange. During low wind speeds (<6 m s−1), water-side convection was found to be a relevant control mechanism. The effect of both sea spray and water-side convection on the gas exchange showed a clear seasonality with positive fluxes (winter conditions) being the most affected.
|
|
| 6. |
- Nilsson, Erik, 1983-, et al.
(författare)
-
Evaluating humidity and sea salt disturbances on CO2 flux measurements
- 2018
-
Ingår i: Journal of Atmospheric and Oceanic Technology. - 0739-0572 .- 1520-0426. ; 35, s. 859-875
-
Tidskriftsartikel (refereegranskat)abstract
- Global oceans are an important sink of atmospheric carbon dioxide (CO2). Therefore, understanding the air-sea flux of CO2 is a vital part in describing the global carbon balance. Eddy covariance (EC) measurements are often used to study CO2 fluxes from both land and ocean. CO2 are usually measured with infrared absorption sensors, which at the same time measure water vapor. Studies have shown that presence of water vapor fluctuations in the sampling air potentially result in erroneous CO2 flux measurements due to cross-sensitivity of the sensor. Here we compare measured CO2 fluxes from both enclosed path Li-Cor 7200 sensors and open-path Li-Cor 7500 instruments from an inland measurement site and a marine site. We also introduce new quality control criteria based upon a Relative Signal Strength Indicator (RSSI). The sampling gas in one of the Li-Cor 7200 instruments was dried by means of a multi-tube diffusion dryer so that the water vapor fluxes were close to zero. With this setup we investigated the effect that cross-sensitivity of the CO2 signal to water vapor can have on the CO2 fluxes. The dryer had no significant effect on the CO2 fluxes. We tested the hypothesis that the cross-sensitivity effect is caused by hygroscopic particles such as sea salt by spraying a saline solution on the windows of the Li-Cor 7200 instruments during the inland field test. Our results confirm earlier findings that sea salt contamination can affect CO2 fluxes significantly and confirm earlier findings, that drying the sampling air for the gas analyzer is an effective method to reduce this signal contamination.
|
|
| 7. |
- Nydahl, Anna C., et al.
(författare)
-
Groundwater carbon within a boreal catchment : spatiotemporal variability of a hidden aquatic carbon pool
- 2020
-
Ingår i: Journal of Geophysical Research - Biogeosciences. - 2169-8953 .- 2169-8961. ; 125:1
-
Tidskriftsartikel (refereegranskat)abstract
- Groundwater is an essential resource providing water for societies and sustaining surface waters. Although groundwater at intermediate depth could be highly influential at regulating lake and river surface water chemistry, studies quantifying organic and inorganic carbon (C) species in intermediate depth groundwater are still rare. Here, we quantified dissolved and gaseous C species in the groundwater of a boreal catchment at 3- to 20-m depth. We found that the partial pressure of carbon dioxide (pCO(2)), the stable carbon isotopic composition of dissolved inorganic carbon (delta C-13-DIC), and pH showed a dependency with depth. Along the depth profile, a negative relationship was observed between pCO(2) and delta C-13-DIC and between pCO(2) and pH. We attribute the negative pCO(2)-pH relationship along the depth gradient to increased silicate weathering and decreased soil respiration. Silicate weathering consumes carbon dioxide (CO2) and release base cations, leading to increased pH and decreased pCO(2). We observed a positive relationship between delta C-13-DIC and depth, potentially due to diffusion-related fractionation in addition to isotopic discrimination during soil respiration. Soil CO2 may diffuse downward, resulting in a fractionation of the delta C-13-DIC. Additionally, the dissolved organic carbon at greater depth may be recalcitrant consisting of old degraded material with a greater fraction of the heavier C isotope. Our study provides increased knowledge about the C biogeochemistry of groundwater at intermediate depth, which is important since these waters likely contribute to the widespread CO2 oversaturation in boreal surface waters.
|
|
| 8. |
- Nydahl, Anna, et al.
(författare)
-
No long-term trends in pCO2 despite increasing organic carbon concentrations in boreal lakes, streams and rivers
- 2017
-
Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 31:6, s. 985-995
-
Tidskriftsartikel (refereegranskat)abstract
- Concentrations of dissolved organic carbon (DOC) from terrestrial sources have been increasing in freshwaters across large parts of the boreal region. According to results from large-scale field and detailed laboratory studies, such a DOC increase could potentially stimulate carbon dioxide (CO2) production, subsequently increasing the partial pressure of CO2 (pCO2) in freshwaters. However, the response of pCO2 to the presently observed long-term increase in DOC in freshwaters is still unknown. Here we tested whether the commonly found spatial DOC-pCO2 relationship is also valid on a temporal scale. Analyzing time series of water chemical data from 71 lakes, 30 streams, and 4 river mouths distributed across all of Sweden over a 17 year period, we observed significant DOC concentration increases in 39 lakes, 15 streams, and 4 river mouths. Significant pCO2 increases were, however, only observed in six of these 58 waters, indicating that long-term DOC increases in Swedish waters are disconnected from temporal pCO2 trends. We suggest that the uncoupling of trends in DOC concentration and pCO2 are a result of increased surface water runoff. When surface water runoff increases, there is likely less CO2 relative to DOC imported from soils into waters due to a changed balance between surface and groundwater flow. Additionally, increased surface water runoff causes faster water flushing through the landscape giving less time for in situ CO2 production in freshwaters. We conclude that pCO2 is presently not following DOC concentration trends, which has important implications for modeling future CO2 emissions from boreal waters.
|
|
| 9. |
- Peacock, Mike, et al.
(författare)
-
Greenhouse gas emissions from urban ponds are driven by nutrient status and hydrology
- 2019
-
Ingår i: Ecosphere. - : Wiley. - 2150-8925 .- 2150-8925. ; 10:3
-
Tidskriftsartikel (refereegranskat)abstract
- Inland waters emit significant quantities of greenhouse gases (GHGs) such as methane (CH4) and carbon dioxide (CO2) to the atmosphere. On a global scale, these emissions are large enough that their contribution to climate change is now recognized by the Intergovernmental Panel on Climate Change. Much of the past focus on GHG emissions from inland waters has focused on lakes, reservoirs, and rivers, and the role of small, artificial waterbodies such as ponds has been overlooked. To investigate the spatial variation in GHG fluxes from artificial ponds, we conducted a synoptic survey of forty urban ponds in a Swedish city. We measured dissolved concentrations of CH4 and CO2, and made complementary measurements of water chemistry. We found that CH4 concentrations were greatest in high‐nutrient ponds (measured as total phosphorus and total organic carbon). For CO2, higher concentrations were associated with silicon and calcium, suggesting that groundwater inputs lead to elevated CO2. When converted to diffusive GHG fluxes, mean emissions were 30.3 mg CH4·m−2·d−1 and 752 mg CO2·m−2·d−1. Although these fluxes are moderately high on an areal basis, upscaling them to all Swedish urban ponds gives an emission of 8336 t CO2eq/yr (±1689) equivalent to 0.1% of Swedish agricultural GHG emissions. Artificial ponds could be important GHG sources in countries with larger proportions of urban land.
|
|
| 10. |
- Venkiteswaran, Jason J., et al.
(författare)
-
Large carbon dioxide fluxes from headwater boreal and sub-boreal streams
- 2014
-
Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 9:7, s. e101756-
-
Tidskriftsartikel (refereegranskat)abstract
- Half of the world's forest is in boreal and sub-boreal ecozones, containing large carbon stores and fluxes. Carbon lost from headwater streams in these forests is underestimated. We apply a simple stable carbon isotope idea for quantifying the CO2 loss from these small streams; it is based only on in-stream samples and integrates over a significant distance upstream. We demonstrate that conventional methods of determining CO2 loss from streams necessarily underestimate the CO2 loss with results from two catchments. Dissolved carbon export from headwater catchments is similar to CO2 loss from stream surfaces. Most of the CO2 originating in high CO2 groundwaters has been lost before typical in-stream sampling occurs. In the Harp Lake catchment in Canada, headwater streams account for 10% of catchment net CO2 uptake. In the Krycklan catchment in Sweden, this more than doubles the CO2 loss from the catchment. Thus, even when corrected for aquatic CO2 loss measured by conventional methods, boreal and sub-boreal forest carbon budgets currently overestimate carbon sequestration on the landscape.
|
|
