| 1. |
- Erlandsson, M., et al.
(författare)
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Spatial and temporal variations of base cation release from chemical weathering on a hillslope scale
- 2016
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Ingår i: Chemical Geology. - : Elsevier BV. - 0009-2541 .- 1872-6836. ; 441, s. 1-13
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Tidskriftsartikel (refereegranskat)abstract
- Cation release rates to catchment runoff from chemical weathering were assessed using an integrated catchment model that included the soil's unsaturated, saturated and riparian zones. In-situ mineral dissolution rates were calculated in these zones as a function of pH, aluminum and dissolved organic carbon (DOC) concentrations along a hillslope in Northern Sweden where soil water was monitored over nine years. Three independent sets of mineral dissolution equations of varying complexity were used: PROFILE, Transition-State Theory (TST), and the Palandri & Kharaka database. Normalization of the rate-coefficients was necessary to compare the equations, as published rate-coefficients gave base cation release rates differing by several orders of magnitude. After normalizing the TST- and Palandri & Kharaka-rate coefficients to match the base cation release rates calculated from the PROFILE-equations, calculated Ca2 + and Mg2 + release rates are consistent with mass balance calculations, whereas those of Na+ and K+ are overestimated. Our calculations further indicate that a significant proportion of base cations are released from the organic soils in the near-stream zone, in part due to its finer texture. Of the three sets of rate equations, the base cation release rates calculated from the normalized TST-equations were more variable than those calculated using the other two sets of equations, both spatially and temporally, due to its higher sensitivity to pH. In contrast, the normalized Palandri & Kharaka-equations were more sensitive to variations in soil temperature.
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| 2. |
- Teutschbein, Claudia, 1985-, et al.
(författare)
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Future Riverine Inorganic Nitrogen Load to the Baltic Sea From Sweden : An Ensemble Approach to Assessing Climate Change Effects
- 2017
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Ingår i: Global Biogeochemical Cycles. - : American Geophysical Union (AGU). - 0886-6236 .- 1944-9224. ; 31:11, s. 1674-1701
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Tidskriftsartikel (refereegranskat)abstract
- The dramatic increase of bioreactive nitrogen entering the Earth’s ecosystems continues toattract growing attention. Increasingly large quantities of inorganic nitrogen are flushed from land towater, accelerating freshwater, and marine eutrophication. Multiple, interacting, and potentiallycountervailing drivers control the future hydrologic export of inorganic nitrogen. In this paper, we attempt toresolve these land-water interactions across boreal/hemiboreal Sweden in the face of a changing climatewith help of a versatile modeling framework to maximize the information value of existing measurementtime series. We combined 6,962 spatially distributed water chemistry observations spread over 31 years withdaily streamflow and air temperature records. An ensemble of climate model projections, hydrologicalsimulations, and several parameter parsimonious regression models was employed to project future riverineinorganic nitrogen dynamics across Sweden. The median predicted increase in total inorganic nitrogenexport from Sweden (2061–2090) due to climate change was 14% (interquartile range 0–29%), based on theensemble of 7,500 different predictions for each study site. The overall export as well as the seasonal patternof inorganic nitrogen loads in a future climate are mostly influenced by longer growing seasons and morewinter flow, which offset the expected decline in spring flood. The predicted increase in inorganic nitrogenloading due to climate change means that the political efforts for reducing anthropogenic nitrogen inputsneed to be increased if ambitions for reducing the eutrophication of the Baltic Sea are to be achieved.
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| 3. |
- Abbott, Benjamin W., et al.
(författare)
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Biomass offsets little or none of permafrost carbon release from soils, streams, and wildfire : an expert assessment
- 2016
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Ingår i: Environmental Research Letters. - : IOP Publishing. - 1748-9326. ; 11:3
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Tidskriftsartikel (refereegranskat)abstract
- As the permafrost region warms, its large organic carbon pool will be increasingly vulnerable to decomposition, combustion, and hydrologic export. Models predict that some portion of this release will be offset by increased production of Arctic and boreal biomass; however, the lack of robust estimates of net carbon balance increases the risk of further overshooting international emissions targets. Precise empirical or model-based assessments of the critical factors driving carbon balance are unlikely in the near future, so to address this gap, we present estimates from 98 permafrost-region experts of the response of biomass, wildfire, and hydrologic carbon flux to climate change. Results suggest that contrary to model projections, total permafrost-region biomass could decrease due to water stress and disturbance, factors that are not adequately incorporated in current models. Assessments indicate that end-of-the-century organic carbon release from Arctic rivers and collapsing coastlines could increase by 75% while carbon loss via burning could increase four-fold. Experts identified water balance, shifts in vegetation community, and permafrost degradation as the key sources of uncertainty in predicting future system response. In combination with previous findings, results suggest the permafrost region will become a carbon source to the atmosphere by 2100 regardless of warming scenario but that 65%-85% of permafrost carbon release can still be avoided if human emissions are actively reduced.
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| 4. |
- van der Velde, Ype, et al.
(författare)
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Consequences of mixing assumptions for time-variable travel time distributions
- 2015
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Ingår i: Hydrological Processes. - : Wiley. - 0885-6087 .- 1099-1085. ; 29:16, s. 3460-3474
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Tidskriftsartikel (refereegranskat)abstract
- The current generation of catchment travel time distribution (TTD) research, integrating nearly three decades of work since publication of Water's Journey from Rain to Stream, seeks to represent the full distribution in catchment travel times and its temporal variability. Here, we compare conceptualizations of increasing complexity with regards to mixing of water storages and evaluate how these assumptions influence time-variable TTD estimates for two catchments with contrasting climates: the Gardsjon catchment in Sweden and the Marshall Gulch catchment in Arizona, USA. Our results highlight that, as long as catchment TTDs cannot be measured directly but need to be inferred from input-output signals of catchments, the inferred catchment TTDs depend strongly on the underlying assumptions of mixing within a catchment. Furthermore, we found that the conceptualization of the evapotranspiration flux strongly influences the inferred travel times of stream discharge. For the wet and forested Gardsjon catchment in Sweden, we inferred that evapotranspiration most likely resembles a completely mixed sample of the water stored in the catchment; however, for the drier Marshall Gulch catchment in Arizona, evapotranspiration predominantly contained the younger water stored in the catchment. For the Marshall Gulch catchment, this higher probability for young water in evapotranspiration resulted in older water in the stream compared to travel times inferred with assumptions of complete mixing. New observations that focus on the TTD of the evapotranspiration flux and the actual travel time of water through a catchment are necessary to improve identification of mixing and consequently travel times of stream water. Copyright (c) 2014 John Wiley & Sons, Ltd.
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| 5. |
- Winterdahl, Mattias, et al.
(författare)
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Riparian Zone Influence on Stream Water Dissolved Organic Carbon Concentrations at the Swedish Integrated Monitoring Sites
- 2011
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Ingår i: Ambio. - : Springer Science and Business Media LLC. - 0044-7447 .- 1654-7209. ; 40:8, s. 920-930
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Tidskriftsartikel (refereegranskat)abstract
- Short-term variability in stream water dissolved organic carbon (DOC) concentrations is controlled by hydrology, climate and atmospheric deposition. Using the Riparian flow-concentration Integration Model (RIM), we evaluated factors controlling stream water DOC in the Swedish Integrated Monitoring (IM) catchments by separating out hydrological effects on stream DOC dynamics. Model residuals were correlated with climate and deposition-related drivers. DOC was most strongly correlated to water flow in the northern catchment (Gammtratten). The southern Aneboda and Kindla catchments had pronounced seasonal DOC signals, which correlated weakly to flow. DOC concentrations at GAyenrdsjon increased, potentially in response to declining acid deposition. Soil temperature correlated strongly with model residuals at all sites. Incorporating soil temperature in RIM improved model performance substantially (20-62% lower median absolute error). According to the simulations, the RIM conceptualization of riparian processes explains between 36% (Kindla) and 61% (Aneboda) of the DOC dynamics at the IM sites.
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| 6. |
- Temnerud, Johan, et al.
(författare)
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Map-based prediction of organic carbon in headwater streams improved by downstream observations from the river outlet
- 2016
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Ingår i: Biogeosciences. - : Copernicus GmbH. - 1726-4170 .- 1726-4189. ; 13:2, s. 399-413
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Tidskriftsartikel (refereegranskat)abstract
- In spite of the great abundance and ecological importance of headwater streams, managers are usually limited by a lack of information about water chemistry in these headwaters. In this study we test whether river outlet chemistry can be used as an additional source of information to improve the prediction of the chemistry of upstream headwaters (size < 2 km(2)), relative to models based on map information alone. We use the concentration of total organic carbon (TOC), an important stream ecosystem parameter, as the target for our study. Between 2000 and 2008, we carried out 17 synoptic surveys in 9 mesoscale catchments (size 32-235 km(2)). Over 900 water samples were collected in total, primarily from headwater streams but also including each catchment's river outlet during every survey. First we used partial least square regression (PLS) to model the distribution (median, interquartile range (IQR)) of headwater stream TOC for a given catchment, based on a large number of candidate variables including sub-catchment characteristics from GIS, and measured river chemistry at the catchment outlet. The best candidate variables from the PLS models were then used in hierarchical linear mixed models (MM) to model TOC in individual headwater streams. Three predictor variables were consistently selected for the MM calibration sets: (1) proportion of forested wetlands in the sub-catchment (positively correlated with headwater stream TOC), (2) proportion of lake surface cover in the sub-catchment (negatively correlated with headwater stream TOC), and (3) river outlet TOC (positively correlated with headwater stream TOC). Including river outlet TOC improved predictions, with 5-15% lower prediction errors than when using map information alone. Thus, data on water chemistry measured at river outlets offer information which can complement GIS-based modelling of headwater stream chemistry.
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| 7. |
- 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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| 8. |
- Temnerud, Johan, et al.
(författare)
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Spatial patterns of some trace elements in four Swedish stream networks
- 2013
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Ingår i: Biogeosciences. - : Copernicus GmbH. - 1726-4170 .- 1726-4189. ; 10, s. 1407-1423
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Tidskriftsartikel (refereegranskat)abstract
- Four river basins in southern Sweden, with catchment sizes from 0.3 to 127 km(2) (median 1.9), were sampled in October 2007. The 243 samples were analysed for 26 trace elements (Ag, As, Au, Ba, Be, Bi, Cd, Co, Cr, Cu, Ga, Ge, In, La, Li, Mo, Ni, Pb, Sb, Se, Sn, Tl, Ti, U, V and Zn) to identify spatial patterns within drainage networks. The range and median of each element were defined for different stream orders, and relationships to catchment characteristics, including deposition history, were explored. The sampling design made it possible to compare the differences along 40 stream reaches, above and below 53 stream junctions with 107 tributaries and between the 77 inlets and outlets of 36 lakes. The largest concentration differences (at reaches, junctions and lakes) were observed for lakes, with outlets usually having lower concentration compared to the inlets for As, Ba, Be, Bi, Cd, Co, Cr, Ga, Ge, Ni, Pb, Sn, Ti, Tl, U, V and Zn. Significantly lower concentrations were observed for Cd and Co when comparing headwaters with downstream sites in each catchment. Common factor analysis (FA) revealed that As, Bi, Cr, Ga, Ge, Tl and V co-vary positively with Al, Fe and total organic carbon (TOC) and negatively with La, Li and pH. The strong removal of a large number of trace elements when passing through lakes is evident though in the FA, where lake surface coverage plots opposite to many of those elements. Forest volume does not respond in a similar systematic fashion and, surprisingly, the amount of wetland does not relate strongly to either Fe or TOC at any of the rivers. A better understanding of the quantitative removal of organic carbon and iron will aid in understanding trace element fluxes from landscapes rich in organic matter and iron.
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| 9. |
- 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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| 10. |
- Ledesma, Jose, et al.
(författare)
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Potential for long-term transfer of dissolved organic carbon from riparian zones to streams in boreal catchments
- 2015
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Ingår i: Global Change Biology. - : Wiley. - 1354-1013 .- 1365-2486. ; 21, s. 2963-2979
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Tidskriftsartikel (refereegranskat)abstract
- Boreal regions store most of the global terrestrial carbon, which can be transferred as dissolved organic carbon (DOC) to inland waters with implications for both aquatic ecology and carbon budgets. Headwater riparian zones (RZ) are important sources of DOC, and often just a narrow ‘dominant source layer' (DSL) within the riparian profile is responsible for most of the DOC export. Two important questions arise: how long boreal RZ could sustain lateral DOC fluxes as the sole source of exported carbon and how its hydromorphological variability influences this role. We estimate theoretical turnover times by comparing carbon pools and lateral exports in the DSL of 13 riparian profiles distributed over a 69km2 catchment in northern Sweden. The thickness of the DSL was 36±18 (average ± SD) cm. Thus, only about one-third of the 1-m-deep riparian profile contributed 90% of the lateral DOC flux. The 13 RZ exported 8.7±6.5g C m-2year-1, covering the whole range of boreal stream DOC exports. The variation could be explained by local hydromorphological characteristics including RZ width (R2=0.90). The estimated theoretical turnover times were hundreds to a few thousands of years, that is there is a potential long-lasting supply of DOC. Estimates of net ecosystem production in the RZ suggest that lateral fluxes, including both organic and inorganic C, could be maintained without drawing down the riparian pools. This was supported by measurements of stream DO14C that indicated modern carbon as the predominant fraction exported, including streams disturbed by ditching. The transfer of DOC into boreal inland waters from new and old carbon sources has a major influence on surface water quality and global carbon balances. This study highlights the importance of local variations in RZ hydromorphology and DSL extent for future DOC fluxes under a changing climate.
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