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1.
Sci Rep ; 13(1): 20218, 2023 Nov 18.
Article in English | MEDLINE | ID: mdl-37980440

ABSTRACT

Drainage for forestry has created ~ 1 million km of artificial waterways in Sweden, making it one of the largest human-induced environmental disturbances in the country. These extensive modifications of both peatland and mineral soil dominated landscapes still carry largely unknown, but potentially enormous environmental legacy effects. However, the consequences of contemporary ditch management strategies, such as hydrological restoration via ditch blocking or enhancing forest drainage to promote biomass production via ditch cleaning, on water resources and greenhouse gas (GHG) fluxes are unclear. To close the gap between science and management, we have developed a unique field research platform to experimentally evaluate key environmental strategies for drained northern landscapes with the aim to avoid further environmental degeneration. The Trollberget Experimental Area (TEA) includes replicated and controlled treatments applied at the catchment scale based on a BACI approach (before-after and control-impact). The treatments represent the dominant ecosystem types impacted by ditching in Sweden and the boreal zone: (1) rewetting of a drained peatland, (2) ditch cleaning in productive upland forests and (3) leaving these ditches unmanaged. Here we describe the TEA platform, report initial results, suggest ways forward for how to best manage this historical large-scale alteration of the boreal landscape, as well as warn against applying these treatments broadly before more long-term results are reported.

2.
Water Res ; 203: 117544, 2021 Sep 15.
Article in English | MEDLINE | ID: mdl-34419921

ABSTRACT

Widespread increases in organic matter (OM) content of surface waters, as measured by color and organic carbon (OC), are a major issue for aquatic ecosystems. Long-term monitoring programs revealed the issue of "brownification", with climate change, land cover changes and recovery from acidification all suspected to be major drivers or contributing factors. While many studies have focused on the impact and drivers, fewer have followed up on whether brownification is continuing. As time-series of OM data lengthen, conventional data-analysis approaches miss important information on when changes occur. To better identify temporal OM patterns during three decades (1990-2020) of systematic monitoring, we used generalized additive models to analyze 164 time-series from watercourses located across Sweden. Increases in OC that were widespread during 1990-2010 ceased a decade ago, and most color increases ceased 20 years ago. These findings highlight the need to reassess the understanding of brownification's spatial and temporal extent, as well as the tools used to analyze lengthening time series.


Subject(s)
Carbon , Ecosystem , Carbon/analysis , Climate Change , Sweden , Water
3.
Water Res ; 200: 117272, 2021 Jul 15.
Article in English | MEDLINE | ID: mdl-34098268

ABSTRACT

Rivers play an important role in global water and carbon cycling, but there are still large uncertainties concerning evaporation and aquatic photosynthesis. Here we combined measurements of water chemistry, isotopic compositions (i.e., δDw, δ18Ow, δ13CDIC and ▵14CDIC) and geographic characteristics (i.e., river width) to elucidate in-stream hydrological and biogeochemical processes across rivers in Hainan Island, China. The results showed that dissolved inorganic carbon (DIC) in river waters was largely of modern origin, with about 95% from contemporary biogenic sources based on an isotopic mass balance of ▵14CDIC. Significant evaporation and aquatic primary production co-occurred in these tropical rivers with large amounts of water and DIC being rapidly turned over in the water column, altering the water cycle and the carbon balance. High rates of evaporation and aquatic primary production were observed in the headwater segments, with narrow river width but broad available reactive surface area at the air-water interface. The asymmetric aquatic photosynthesis at different river segments caused the spatial heterogeneities of dissolved solutes. The results suggest that the available reactive area at the water-air interface is responsible for synchronous water loss and dissolved carbon evolution in flat tropical rivers. This study provides evidence that intense evaporation and aquatic photosynthesis mainly occurred in headwater segments, which has implications for understanding global carbon cycling.


Subject(s)
Carbon Cycle , Rivers , Carbon/analysis , Carbon Isotopes/analysis , China , Environmental Monitoring
4.
Glob Chang Biol ; 26(2): 629-641, 2020 02.
Article in English | MEDLINE | ID: mdl-31465582

ABSTRACT

Streams and river networks are increasingly recognized as significant sources for the greenhouse gas nitrous oxide (N2 O). N2 O 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 N2 O emissions from forest streams although they constitute a major part of the total stream network globally. Here, we compiled N2 O 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 N2 O 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 N2 O concentrations and environmental variables were difficult to discern, the percent saturation of N2 O 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 N2 O 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 N2 O emissions. An estimate of the N2 O emission from low-order streams at the national scale revealed that ~1.8 × 109  g N2 O-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 N2 O sources in the landscape with 800 × 109  g CO2 -eq emitted annually in Sweden, equivalent to 25% of the total N2 O emissions from the Swedish agricultural sector.


Subject(s)
Forests , Nitrous Oxide , Fertilizers , Soil , Sweden
5.
Sci Rep ; 8(1): 16060, 2018 10 30.
Article in English | MEDLINE | ID: mdl-30375497

ABSTRACT

Dissolved organic matter (DOM) from soils enters the aquatic environment via headwater streams. Thereafter, it is gradually transformed, removed by sedimentation, and mineralised. Due to the proximity to the terrestrial source and short water residence time, the extent of transformation is minimal in headwaters. DOM has variable composition across inland waters, but the amount of variability in the terrestrial end member is unknown. This gap in knowledge is crucial considering the potential impact large variability would have on modelling DOM degradation. Here, we used a novel liquid chromatography -mass spectrometry method to characterise DOM in 74 randomly selected, forested headwater streams in an 87,000 km2 region of southeast Sweden. We found a large degree of sample similarity across this region, with Bray-Curtis dissimilarity values averaging 8.4 ± 3.0% (mean ± SD). The identified variability could be reduced to two principle coordinates, correlating to varying groundwater flow-paths and regional mean temperature. Our results indicate that despite reproducible effects of groundwater geochemistry and climate, the composition of DOM is remarkably similar across catchments already as it leaves the terrestrial environment, rather than becoming homogeneous as different headwaters and sub-catchments mix.

6.
Sci Rep ; 7(1): 9158, 2017 08 22.
Article in English | MEDLINE | ID: mdl-28831088

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 δ13C-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 δ13C-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.

7.
Glob Chang Biol ; 23(12): 5523-5536, 2017 12.
Article in English | MEDLINE | ID: mdl-28712133

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 (14 C) of dissolved organic carbon (DOC), carbon dioxide (CO2 ), and methane (CH4 ) exported from a boreal peatland catchment coupled with 14 C 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 14 C 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.


Subject(s)
Carbon Dioxide/chemistry , Carbon/chemistry , Climate Change , Methane/chemistry , Soil , Wetlands , Atmosphere , Carbon Cycle , Carbon Dioxide/metabolism , Environmental Monitoring , Gases , Methane/metabolism
8.
Sci Rep ; 7: 39729, 2017 01 03.
Article in English | MEDLINE | ID: mdl-28045092

ABSTRACT

Global stream and river greenhouse gas emissions seem to be as large as the oceanic C uptake. However, stream and river emissions are uncertain until both spatial and temporal variability have been quantified. Here we investigated in detail the stream CH4 and CO2 emissions within a hemiboreal catchment in Southwest Sweden primarily covered by coniferous forest. Gas transfer velocities (k600), CH4 and CO2 concentrations were measured with multiple methods. Our data supported modelling approaches accounting for various stream slopes, water velocities and discharge. The results revealed large but partially predictable spatio-temporal variabilities in k600, dissolved gas concentrations, and emissions. The variability in CO2 emission was best explained by the variability in k, while dissolved CH4 concentrations explained most of the variability in CH4 emission, having implications for future measurements. There were disproportionately large emissions from high slope stream reaches including waterfalls, and from high discharge events. In the catchment, stream reaches with low slope and time periods of moderate discharge dominated (90% of area and 69% of time). Measurements in these stream areas and time periods only accounted for <36% of the total estimated emissions. Hence, not accounting for local or episodic high emissions can lead to substantially underestimated emissions.

9.
PLoS One ; 9(7): e101756, 2014.
Article in English | MEDLINE | ID: mdl-25058488

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.


Subject(s)
Carbon Cycle , Carbon Dioxide/chemistry , Carbon/chemistry , Models, Statistical , Rivers/chemistry , Soil/chemistry , Carbon Isotopes , Environmental Monitoring , Forests , Seasons , Sweden
10.
Glob Chang Biol ; 19(3): 785-97, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23504836

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 km(2) boreal catchment was studied. During a 4 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 first- and second-order streams. This study demonstrates the importance of including CO2 evasion from low-order boreal streams into landscape C budgets as 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.


Subject(s)
Carbon Dioxide/analysis , Carbon/analysis , Rivers/chemistry , Soil/analysis
11.
Environ Sci Technol ; 43(19): 7364-9, 2009 Oct 01.
Article in English | MEDLINE | ID: mdl-19848147

ABSTRACT

The aim of this investigation was to determine the lateral exportof 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 m 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(l) = 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.


Subject(s)
Carbon/chemistry , Rivers/chemistry , Soil/analysis , Arctic Regions , Ecosystem , Environmental Monitoring
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