Articles | Volume 17, issue 3
Research article
10 Feb 2020
Research article |  | 10 Feb 2020

Low methane emissions from a boreal wetland constructed on oil sand mine tailings

M. Graham Clark, Elyn R. Humphreys, and Sean K. Carey

A 58 ha mixed upland and lowland boreal plains watershed called the Sandhill Fen Watershed was constructed between 2008 and 2012. In the years following wetting in 2013, methane emissions were measured using manual chambers. The presence of vegetation with aerenchymous tissues and saturated soils were important factors influencing the spatial variability of methane emissions across the constructed watershed. Nevertheless, median methane emissions were equal to or less than 0.51 mg CH4 m−2 h−1 even from the saturated organic soils in the lowlands. Although overall methane emissions remained low, observations of methane ebullition increased over the 3 study years. Ebullition events occurred in 10 % of measurements in 2013, increasing to 21 % and 27 % of measurements in 2014 and 2015, respectively, at the plots with saturated soils. Increasing metal ion availability and decreasing sulfur availability was measured using buried ion exchange resins at both seasonal and annual timescales potentially as a result of microbial reduction of these ions. Using principle component analysis, methane fluxes had a significant positive correlation to the leading principle component which was associated with increasing ammonium, iron, and manganese and decreasing sulfur availability (r=0.31, p<0.001). These results suggest that an abundance of alternative inorganic electron acceptors may be limiting methanogenesis at this time.

1 Introduction

The boreal biome stores large quantities of soil carbon (C) due to the high density of peatlands with some estimates as high as 165 kg C m−2 (Beilman et al., 2008). A legacy of open pit oil sands mining in northern Alberta, Canada, will be that almost 5000 km2 of the boreal landscape (Alberta Government, 2017) will require reclamation to restore it to the “equivalent capability” of the pre-mining ecosystems (Environmental Protection and Enhancement Act, 2017). These engineered landscapes will be important in determining the long-term C footprint of the region, potentially helping to offset ecological losses and industrial emissions. Rooney et al. (2012) used land cover classification and reclamation plans to estimate a potential net loss of 11.4–47.3 Tg of the stored soil C from the pre-mining landscape and a reduction in CO2 sequestration capacity of the new constructed landscape by 5.7–7.2 Gg C yr−1. This loss is expected to occur as a result of both the decomposition of peat when it is used in the reclamation of uplands and from the diminished C sequestration capacity of engineered landscapes. In particular, Rooney et al. (2012) predicted that an insufficient proportion of the disturbed area will be replaced with the C sequestration capacity of the original boreal wetlands. However, wetland reclamation in the region is still quite novel, and little is known about the surface–atmosphere exchange of C in these newly engineered wetlands (Nwaishi et al., 2015; Clark et al., 2019).

Undisturbed peatlands are long-term CO2 sinks, accumulating C as peat over millennia (Rydin and Jeglum, 2006; Vasander and Kettunen, 2006). Yet, on annual timescales the C cycling within peatlands is highly variable and only partially understood, particularly with regards to methane (CH4) emissions (Vasander and Kettunen, 2006). Wetland CH4 emissions are thought to be the single greatest driver of inter-annual variability in atmospheric CH4 concentration (Bousquet et al., 2006), and globally wetlands are the largest non-anthropogenic source of CH4 to the atmosphere (Kirschke et al., 2013). Atmospheric CH4 has 28–34 times the global warming potential of CO2 over a 100-year time period but with a perturbation lifetime of 12.4 years in the atmosphere, and its radiative forcing is much greater on decadal timescales (IPCC, 2013). Therefore, CH4 production and release is an important land–atmosphere climate change feedback process (Kirschke et al., 2013). Since methanogenesis is only favoured at the lowest reduction–oxidation (REDOX) potentials known to support life, the high rates of CH4 emission and low rates of C turnover in peatlands are linked to a scarcity of inorganic electron acceptors in anoxic, saturated soils (Hahn-Schöfl et al., 2011; Peters and Conrad, 1995; Thomas et al., 2009). Around the time that Rooney et al. (2012) estimated the C balance for the post-mining landscapes of Alberta, the first two large-scale wetlands were being constructed in the Fort McMurray region. These wetlands were designed and constructed to test theories on how to return the peat-forming and C-capturing capacities to the mined landscape (Wytrykush et al., 2012). A research gap exists, however, between the modelled predictions of C cycling by Rooney et al. (2012) and the actual C cycling of constructed wetlands. Clark et al. (2019) discussed the increasing CO2 sink strength over the first 3 years of one of these wetlands but did not address emissions of CH4, which can contribute substantially towards the long-term C balance of some ecosystems (Vasander and Kettunen, 2006). The aim of this study is to evaluate CH4 emissions from this constructed ecosystem and identify the factors which influence their temporal and spatial variability.

Methane emissions from wetlands are highly variable in space and time (Moore et al., 1998). Four key wetland characteristics are typically linked to the temporal and spatial variability of CH4 flux in peatlands: water table position, REDOX, vegetation composition, and temperature (Ding et al., 2005; Kim et al., 2012; Limpens et al., 2008; Turetsky et al., 2014; Vasander and Kettunen, 2006). Approximately 60 % to 90 % of the CH4 produced in peatlands is reoxidized before it reaches the atmosphere (Le Mer and Roger, 2001). Emissions tend to be higher in areas with a high water table as this limits the potential for CH4 oxidation (Moore et al., 2011), while deep rooting vegetation with aerenchymatous tissues (Couwenberg, 2009; Kludze et al., 1993) allow CH4 to bypass the aerated surface peat where aerobic methanotrophic communities reside. Aerenchymatous tissues can also transport oxygen into the rhizosphere, which can increase REDOX potentials and create unfavourable niches for anaerobic microbial communities (Blossfeld et al., 2011). Rhizospheric microbial communities readily metabolize the labile organic compounds exuded by roots such that plant net primary productivity is positively correlated with CH4 production (Dacey et al., 1994; Megonigal and Schlesinger, 1997; Vann and Megonigal, 2003; e.g. Whiting and Chanton, 1993; Ziska et al., 1998). Numerous studies have also shown CH4 emissions increase in warmer soils (Bubier et al., 2005; Bubier and Moore, 1994; Roulet et al., 1992; Whalen, 2005; Whiting and Chanton, 1993), although this effect may be masked when water table or other environmental factors co-vary (Moore et al., 2011).

Although constructed peatlands are relatively novel, restoration of peatlands has occurred for decades by rewetting drained peat, often by blocking the ditches originally used to drain them (Rochefort and Lode, 2006). In a comprehensive review of the literature, the IPCC suggested that CH4 emission rates from rewetted boreal sites with rich organic soils can be estimated as 2.1 mg CH4 m−2 h−1 but encourage site-specific study because the range in the published literature is very large and not normally distributed (IPCC, 2014). A follow-up review of the literature by Wilson et al. (2016) provided additional evidence that CH4 emissions were 1.7 to 22.6 times greater for rewetted vs. drained boreal organic soils. The data examined by Wilson et al. (2016) were extrapolated using models of average area (to include multiple surface types) and annual rates, to conform with IPCC reporting standards. Our review of paired studies which directly compare rewetted and drained environments shows that rewetted boreal and temperate organic soils have an average of 23 and 64 times the CH4 emissions of their drained counterparts, respectively (Table S1 in the Supplement). However these differences in CH4 emissions are highly variable and some studies show a decrease in CH4 emissions after wetting (Christen et al., 2016; Juottonen et al., 2012; Urbanová et al., 2012; Waddington and Day, 2007). The few studies which compare emissions from rewetted and undisturbed wetlands (Table S1) show a wide range of results with rewetted wetland emissions <1 % (Juottonen et al., 2012), 19 % (Beetz et al., 2013), 43 % (Urbanová et al., 2012), and 127 % (Christen et al., 2016) of the emissions observed in undisturbed wetlands.

To determine the CH4 emissions of a closure watershed in the oil sands mining region of northern Alberta and how these emissions compare to those from the restored peatlands listed above, this paper presents 3 years (2013–2015) of CH4 emission measurements from the Sandhill Fen Watershed (SFW), one of the first wetland complexes constructed in the Athabasca oil sands region (AOSR). Once water was added to the SFW, approximately 17 ha of the 58 ha construction had permanently saturated peat soils with little horizontal or vertical water flow (Nicholls et al., 2016) and thriving plant communities including species with aerenchyma (e.g. Carex spp.) (Vitt et al., 2016). We hypothesized that these areas would be a significant source of CH4 and these CH4 emissions would be an important component of the C balance of the SFW. Results of this research will provide important information on the greenhouse gas and C budget for reclamation ecosystems in the AOSR and help guide future strategies for ecosystem design and C management.

2 Study site

The SFW (57.0403 N, 111.5890 W) was designed to reclaim sand-capped soft tailings with the conditions needed to promote the long-term development of a peat-forming boreal plains ecosystem (Wytrykush et al., 2012). Details of the SFW construction were described by Wytrykush et al. (2012) and others (Biagi et al., 2019; Nicholls et al., 2016; Oswald and Carey, 2016; Vitt et al., 2016). Clark et al. (2019) described the three main topographic features of the SFW as a lowland region (the wetland), a midland region (drained but moist organic soils), and an upland region lying 2 to 6 m above the wetland with well-drained sandy soils and two experimental perched wetland sites with moist organic soils (Fig. 1). The sand of the lowland, midland, and perched wetland regions was covered with 0.5 to 1 m of peat coarsely mixed with some underlying mineral soil via excavation of nearby peatlands before mining. A goal of the SFW design was to limit vertical transport of tailings and process-affected waters (i.e. water with some component of industrial wastewater known to contain salts and naphthenic acids) to the surface (Wytrykush et al., 2012). To achieve this, fine sediments with 26.4 %–46.4 % clay (based on texture analysis) were placed in the lowland regions of the SFW to help minimize vertical transport of process-affected waters from the tailings below.

Figure 1Map of the Sandhill Fen Watershed. Standing water was limited to the lowland region only.

Initially, freshwater was pumped into the containment pond in the west end of the SFW in 2013 (Fig. 1). This water flowed through a leaky gravel dam into the SFW to initially saturate the lowland region. A downstream pump was used to remove water from an outlet V-notched weir (Fig. 1). Except for a few hours of operation, the pumps were not used in 2014 or 2015. Four underdrains, which run along the central area of the lowland region, were placed to limit the upwelling of the salt-rich process water. The underdrains were not operated after the beginning of the 2014 growing season.

After placement and before wetting, the top 0.25 m of the donor peat/mineral material in the midland and lowland had a mean (± SD) C-to-nitrogen (N) ratio of 22.7 (±3.4), N content was 0.98 (±0.36) % by dry weight, Ca and Na concentrations were 786.1 (±409.4) and 184.2 (±79.0) mg kg−1, respectively, and electrical conductivity was 1980 (±600) µS cm−1 (n=107). The concentration of Fe was 8028 (±2712, n=13) mg kg−1 and SO42- concentration was high, with a mean of 914.0 (±425.5, n=107) mg S kg−1. Total S concentration by dry weight was also high at 1.00 % (±0.50 %, n=12) determined by oxidation in an induction furnace then quantified through infrared mass spectroscopy with a LECO IR (LECO Corporation, Saint Joseph, MI).

In the third growing season (2015) since the ecosystem was seeded/planted (see Vitt et al., 2016, for more details), there were four distinct plant communities in the lowland roughly distributed along a soil moisture and water depth gradient (Vitt et al., 2016). The areas with standing water (Fig. 1) were dominated by Carex aquatilis Wahlenb., Typha latifolia L., and to a lesser extent Carex utriculata Stokes, while areas with the water table near the surface contained the most species associated with peatlands including sedges and bryophytes (Vitt et al., 2016). The drier areas contained the largest percentage of weedy species, or species not associated with peatlands (Vitt et al., 2016). The midland and organic soil regions of the upland were populated by planted trees (Populus tremuloides Michx., Betula papyrifera Marshall, Picea glauca Monech, Picea mariana Mill., Larix laricina Du Roi, and Pinus banksiana Lamb.) and local grasses (e.g. Hordeum jubatum L.) that had naturally colonized the region. Vegetation cover throughout the whole watershed increased over time; peak season leaf area index increased from 1.5±0.6 to 2.2±1.1 over the 3 years as measured at 15 plots (5 midland, 10 lowland) using a plant canopy analyzer (LAI-2200, LI-COR Inc., Lincoln, NE).

3 Materials and methods

This study used plot-scale measurements of CH4 fluxes over 3 years to assess the temporal and spatial variations in CH4 emissions and the factors that influence their variability. Fluxes were measured using non-steady-state static chambers following methods described by Wilson and Humphreys (2010). Plots were established over the 3 years of study to sample the dominant landforms and built features of the SFW. In 2013, 15 plots were established across the lowland and midland of the SFW. In 2014, the number of plots was increased to 21 by including plots on the organic soils in the perched wetlands (upland region) and in 2015 was increased to 29 by adding more plots in the lowland (Fig. 1). The 2013 plots were chosen before the pumps were activated and were selected to capture the surface moisture and vegetation heterogeneity while maintaining multiple plots on similar landforms. The midland plots were chosen to capture differences in the vegetative cover. Two plots were placed on sandy soils, one directly on exposed tailings sand and the other on the salvaged mineral soil mixture. In 2014, the new collars were placed on the experimental wetland sites that were depressions built into the upland hills. Note that these upland plots remained moist but well drained for the duration of the measurements. The eight new collars in the lowland added in 2015 were placed along a moisture gradient transect also used for REDOX monitoring (described below).

The midland plots had water table depths over 0.5 m below the surface and all upland plots had water table depths exceeding 1 m. For the remainder of this paper, midland and upland plots were combined into one group called “upland” due to their similar soil, water table depth, and vegetation characteristics. In the lowland, the “saturated” plots were those with volumetric soil water content ≥86 % (i.e. fully saturated), and all remaining plots were part of the “unsaturated” group. Only five lowland plots switched categories in 2013 and early spring 2014 and 2015, all periods when CH4 emissions were uniformly low with no discernible differences among the groups. Water table depth was not monitored at each plot, but the soil moisture measurement method is described below.

Each plot included a pair of 0.19 m tall collars with a surface area of 0.07 m2 that were inserted until nearly flush with the soil surface to minimize changes to the microclimate as a result of the collar (Parkin and Venterea, 2010). Each pair consisted of one collar that was maintained free of vegetation by clipping and the other was left undisturbed (Fig. 2). A limitation of the undisturbed collar was that any vegetation larger than the flux chambers (0.4 m tall, 0.03 m3) was trimmed to fit within the chamber. This trimming had the largest effect in the lowland, where some Typha died once trimmed. The collars were made of SDR35 12” PVC sewer pipe with a groove cut into the top edge where an acrylic chamber was placed during measurement. The chambers were constructed of acrylic and were covered in opaque black plastic to reduce heating within the chamber and eliminate photosynthetic uptake of CO2 for a respiration analysis discussed by Clark et al. (2019). A seal between the chamber and collar was made by filling the groove with water. A small coiled vent tube on the top of the chamber maintained equal pressure with the surroundings (Hutchinson and Livingston, 2001). During a measurement, the air inside the chamber was mixed by pumping a 60 mL syringe connected to the chamber sampling line and then pulling 24 mL of air from the chamber volume at 0, 5, 10, 15, and 20 min intervals. The sampled air was injected into a 12 mL evacuated vial containing a small amount of magnesium perchlorate to remove any water vapour from the air sample. Flux measurements were made between late May and early August in all 3 years, referred to hereafter as the growing season. The air samples were transported to Carleton University where CO2 and CH4 concentrations were measured on a gas chromatograph (CP 3800, Varian, CA) within a few months of sampling. The operational details of the gas chromatograph (GC) are described in Wilson and Humphreys (2010).

Figure 2Example of a plot with a collar pair in the wetland area illustrating a collar excluding vegetation (on the left) and a vegetated collar (right) and surface PRS probes (orange and purple tabs with orange flagging tape; locations outside the collar are marked with circles). The permanent soil thermocouple profile post is marked by an “X”. This plot is from the lowland unsaturated category (bottom of the easternmost boardwalk, Fig. 1), and the photograph was taken on 3 July 2015.


During the initial collar installation, five thermocouples were buried to a depth of 2, 5, 10, 20, and 50 cm at each plot between the two collars. At the time chamber flux measurements were made, soil temperatures were recorded from the buried thermocouples. A portable soil water sensor that integrated over the upper 0.2 m of soil (HydroSense, Campbell Scientific Inc., Utah, USA) was used to measure volumetric water content of the soil at three locations surrounding each of the collars. When there was standing water over 0.05 m deep, no manual soil water measurements were made. In those cases, the soil moisture was estimated at 87 % (an estimate of saturated conditions based on an average soil bulk density of 0.28 g cm−3).

Fluxes in units of mg C-CH4 m−2 h−1 were calculated from the linear rate of change in CH4 mixing ratios (nmol CH4 mol−1 air), the molar density of the air in the chamber (mol air m−3), the chamber volume (m3) and area (m2), and the molecular weight of carbon (mg C nmol−1CH4). To determine air density, barometric pressure was recorded at a nearby micrometeorological station (Fig. 1) and chamber temperature was estimated using the 0.02 m thermocouple at each plot. The chamber volume was adjusted for the different collar heights and depth of standing water. All calculations and statistical analyses were carried out with MATLAB 2015 (MathWorks Inc., Massachusetts, USA).

The R2 coefficient from the linear regression of CH4 concentration over time is not suitable as a quality control metric by itself (Lai et al., 2012). For example, when the fluxes approach zero, the slope also approaches zero and small variability in gas concentrations results in low R2 values. In total, 16 % of the fluxes had an R2 over 0.9 % and 28 % over 0.8. Instead of the typical R2 filtering, quality control of the data was done by a visual inspection of each time series used to calculate the fluxes. Any flux measurement which had a distinctly non-monotonic or non-linear trend due to individual data point anomalies was removed from further analysis (6.4 %, 12.3 %, and 11.2 % of the flux measurements in 2013, 2014, and 2015, respectively). These anomalies included isolated large decreases in concentration or a return to ambient concentration or isolated or unsustained large increases in concentration and represented fluxes from a leaking chamber or an ebullition event (Tokida et al., 2007). In 2013 REDOX potential was measured every 15 min with nine HYPNOS III rods (Vorenhout et al., 2011) inserted into the soil every 2 m alongside the 20 m transect of new plots to evaluate the impacts of a moisture gradient on CH4 emissions (Fig. 1). The HYPNOS rods were equipped with four platinum probes and thermistor temperature sensors, of which the sensors 0.2 and 0.4 m below the surface were used in this study. The reference was a pH probe with a 0.1 M KCl standard buried below the water table near the middle of the transect. The probes were connected to two HYPNOS data loggers and the standardized REDOX potentials (n=36) were calculated as the sum of the measured potential and the reference potential. No pH correction was applied to probe measurements because pore water remained circumneutral and stable throughout the season. During summer 2015, the mean pH was 7.1±0.4 (± SD) as determined using weekly measurements at a nearby pore water sampling well that integrates the water from ∼1 m depth to the surface. Early spring (20 May) had the largest discrepancy between the well and surface water measurement locations, with the surface water at a pH of 7.6 and the well water at 6.2. By early July the two sampling locations had almost converged at neutral, with a slightly higher pH in the surface water ( 7.4 vs. 6.9).

Within each plot, three replicate sets of plant root simulator (PRS) probes (Western Ag., Saskatoon, Canada) were buried at a depth of 0.1 m (shallow) and 0.2 m (deep) outside the collars. PRS probes are ion exchange membranes designed to mimic in situ soil–root exchange of nutrients and other ions in a non-destructive manner (Qian et al., 2008; Qian and Schoenau, 2005). PRS probes provide a time-integrated representation of the soil nutrient availability and net adsorption rates in units of ion mass per membrane area per burial time. These values differ from the more common point-in-time soil extraction measurements (typically element mass per mass of dry soil), although studies show good correspondence between methods for N, P, K, and S (Harrison and Maynard, 2014; Qian et al., 1992). The probes were buried for 28 d ( 1 month), with three consecutive burial periods monitored each year starting on days 149, 146, and 146 for 2013, 2014, and 2015, respectively. For simplicity, since the midpoint of each of these three 1-month burial periods corresponds roughly to the start of June, July, and August, results from each period were referred to as the result from those months (i.e. the July ion adsorption rate refers to the moles of ions absorbed by the PRS probe period between the 174th and 202nd days of the year). An example plot with collars, PRS probes, and thermocouples is shown in Fig. 2.

Temporal trends in the PRS probe ion data were assessed using Spearman rank correlations using three different temporal groupings of the data. First, the data were binned into categories 1 to 9, representing each of the 3 months across 3 years of measurements (for example, June of the third year was category 7). Second, the data were binned into three categories corresponding to the 3 months of measurements each year, regardless of year, to ignore the inter-annual trends. Finally, the data were binned by year, regardless of the collection month, to ignore the monthly and seasonal trends. This allowed some quantification of the seasonal trends relative to the inter-annual trends in all three groups (upland and the saturated and unsaturated lowland groups).

To relate CH4 fluxes, REDOX, and PRS probe results, a principal component analysis (PCA) was performed on the standardized measurements (z scores) of net ion adsorption rates from the PRS probes buried at 0.2 m depth in the nine plots with REDOX probes. The availability of alternative electron acceptors including NH4+, Mn4+, Fe3+, and SO42- are linked to varying soil REDOX potential through their participation in microbially mediated REDOX reactions. It should be noted that although PRS probes adsorb all mobile forms of S, most are expected to be SO42- (Li et al., 2001). Using Pearson correlation, the relationship between the leading two principal components and 0.2 m REDOX measurements were assessed. Pearson correlation was also used to assess the relationship between the leading two principal components and the log-transformed CH4 flux (transformed to account for skew) averaged over the burial period. Methane fluxes were increased by a common absolute value of the minimum flux observed in the study (−0.10 mg C-CH4 m−2 h−1) to permit the log transformation. Pearson correlation was also used to assess any linear relationships between the transformed CH4 flux and soil moisture and 0.02 m soil temperature. Individual Pearson correlations were calculated between the mean transformed CH4 flux and the net ion adsorption rates at the two burial depths for a burial period.

The effects of vegetation and standing water on CH4 fluxes were evaluated using a linear mixed-effect (LME) model:

(1) methane flux i j = α i j + ζ 0 j + β 1 v e g e t a t e d i j + β 2 s a t u r a t e d i j + ϵ i j ,

where vegetated and saturated were binary vectors indicating if the measurement comes from a vegetated plot or a saturated plot, respectively. i and j subscripts represent measurements from each sampling day and site, respectively. β is the slope of the fixed effect, ε the residual, α the intercept, and ζ the random effect from the repeated measures occurring at each site.

An independent but similar LME model was constructed to detect significant effects of soil depth and standing water on PRS net ion adsorption rates and REDOX potentials; the vegetated covariate was replaced with the binary vector deep, which represented the relative depth of the REDOX or PRS measurement (i.e. deep or shallow):

(2) PRS ion / REDOX potential i j = α i j + ζ 0 j + β 1 d e e p i j + β 2 s a t u r a t e d i j + ϵ i j .
4 Results

The three growing seasons (1 May through 31 September) were warmer and wetter than the long-term average. The average air temperatures recorded at 3 m above the lowland were 16.4, 15.3, and 15.3 C and total rainfall was 375.1, 299.1, and 231.3 mm for the 2013, 2014, and 2015 growing seasons, respectively. The 1981–2010 climate normal for this period was 13.3 C and 211.1 mm at a nearby weather station (Fort McMurray Airport; 48 km from study area; Environment and Climate Change Canada, 2016). Over the 3-year study period, the upland plot soils were drier and slightly warmer than the lowland plots with an average volumetric soil moisture of 34.7 % compared to the 57.5 % in the lowland (Table 1). There were only small differences in growing season 0.02 m soil temperatures at the plot level (Table 1). Near the climate monitoring station in the centre of the lowland the electrical conductivity was measured to be 1171±269, 2109±306, and 2163±248µS cm−1 in 2013, 2014, and 2015, respectively, where the typical electrical conductivity of boreal wetland pore waters ranges from 400 to 2770 µS cm−1 (Trites and Bayley, 2009).

Table 1Soil and CH4 flux characteristics of the three location groups. The standard deviation from the mean is reported in brackets. Dominant vegetation is the most common plant type among the vegetated collars (by percentage of cover).

a As the water table declined, plots were reclassified as unsaturated in the lowland at the time of sampling. Therefore, the sum of the groups each year exceeds the number of chambers reported in the text for that year. b When standing water was observed, soil moisture was not measured, and the volumetric soil moisture was set to 87 %. The depth of standing water varied from 0.03 to 0.33 m.

Download Print Version | Download XLSX

4.1 Spatial and temporal CH4 and ion relationships in the SFW

During each growing season, CH4 emissions were generally very low, with median values less than or equal to 0.04 mg C-CH4 m−2 h−1 for all plot groups (Table 1). The greatest median CH4 emissions were from the saturated plots (all located in the lowland) in July 2015 with median emissions reaching 0.51 mg C-CH4 m−2 h−1 (Fig. 3).

Figure 3Water table, precipitation, and median CH4 fluxes by sampling date. Water table depth and precipitation (a) were measured at the central meteorological station (Fig. 1). Circles indicate median CH4 flux on the day of sampling, and lines indicate the 25th to 75th percentiles for collars with vegetation (b) and collars maintained free of vegetation (c). An offset between vegetation groups has been added to the x axis to reduce overlapping points. All groups were sampled on the same day, roughly once a week. Tick marks on the x axis indicate first day of the labelled month. If the upper 75th percentile exceeded the range of the y axis, the value is printed on the plot.


The proportion of measurements where substantive CH4 emissions were detected increased for the saturated plots over the study period (Table 1). This included occasions with ebullition or when fluxes were greater than 0.5 mg C-CH4 m−2 h−1, which is equivalent to 10 times the maximum CH4 uptake rate observed at this site and is in the upper range of average uptake rates observed in grassland and forest soils around the world (Yu et al., 2017). Among all three groups and years, the 2015 saturated plots had the highest proportion of CH4 emissions exceeding 0.5 mg C-CH4 m−2 h−1 (6.5 %) and the highest number of ebullition events (26.6 %). Vegetated collars had a higher median CH4 flux than in collars with vegetation excluded, particularly in the saturated plots (Fig. 3). There appeared to be an increase in CH4 emissions over time in the vegetated collars within the saturated plots both within the growing season and inter-annually.

The rates of Mn2+, Fe2+, and NH4+ ion adsorption on the PRS probes were greatest in the saturated lowland plots and lowest in the upland plots. By 2015, net adsorption of S was lower in the saturated lowland plots than in the upland plots (Fig. 4). The ion with the strongest absolute temporal trend in adsorption was S (Table 2, Fig. 4), with most of this trend likely a result of changes in SO42- availability (Geer and Schoenau, 1994; Li et al., 2001). In the saturated plots, mobile S decreased seasonally, annually, and over the duration of the study (the greatest Spearman rank coefficient was for 0.25 m deep S ion adsorption rates and chronological time represented as increasing values 1 through 9, Table 2). Declines in net S adsorption were also observed in the other plot groups but the greatest decline was in the saturated lowland plots, where, relative to 2013 values, 2014 values were 40 % lower and 2015 values were 50 % lower (Table 1 and Fig. 4). Correspondingly, net adsorption rates for Mn2+, Fe2+, and NH4+ ions significantly increased over time at the saturated plots (Table 2).

Table 2Spearman rank correlations to assess temporal trends in net ion adsorption rates for the three plot groups. Plant root simulator (PRS) data were categorized into chronological order (1–9 for the three burial periods over 3 years, “Combined”), seasonal order regardless of year (1–3, “Seasonal”), and annual order regardless of season (1–3, “Annual”). Bold values indicate a significant trend at α=0.01. The greatest temporal trend across all plot groups for a given ion and depth is in italic.

Download Print Version | Download XLSX

Figure 4Ion availability as measured using plant root simulator ion exchange resins over the three monthly burial periods for 3 years expressed in units of µg 10 cm−2 per month at two depths (0.1 and 0.2 m). Units are a function of time the probes were buried for. Metal ions were measured in their reduced forms and mobile S is the oxidized form of sulfur. An offset has been added between groups on the x axis to reduce overlapping points.


4.2 Spatial and temporal relationships along a moisture gradient in the lowland

Along the moisture gradient established by a slightly sloping surface in the north-eastern part of the lowland (Fig. 1), CH4 emissions were higher in the four saturated plots than in the five unsaturated plots (Fig. 5). Methane emissions were also higher in vegetated collars than in collars with vegetation excluded. Using a LME model (Eq. 1), and controlling for sampling location as a random effect, CH4 emissions were 0.34±0.11 mg m−2 h−1 greater in saturated plots than unsaturated plots and 0.17±0.06 mg m−2 h−1 greater in vegetated collars than collars without vegetation over the August period (Table 3), when CH4 fluxes were greatest, in both magnitude and proportion of emissions exceeding 0.5 mg C-CH4 m−2 h−1 (Table 1). Temperature and soil moisture were also included in an earlier version of the LME model, but they did not have a significant effect on CH4 emissions so were removed from the model.

Table 3Results of the linear mixed-effect models for CH4 emissions, PRS ions, and REDOX potential (Eqs. 1 and 2) measured August 2015 at the nine plots along the moisture gradient in the lowland of the Sandhill Fen Watershed. Values are the mean effect ± the standard deviation. Bold values indicate parameters significantly different from zero at the α=0.05 level. Vegetation effects are only for the CH4 emission model (Eq. 1). Plot effect is the standard deviation of the random effects from each plot.

Download Print Version | Download XLSX

Figure 5CH4 fluxes (a), net rates of ion adsorption measured with PRS ion exchange resins (b, c, d), and the REDOX potential (e) measured every 15 min at 0.2 and 0.4 m over the burial period in the lowland moisture gradient plots in August 2015. Box plots represent the interquartile range, with whiskers as 95 % and lines representing the median for the nine plots (n=4 for the saturated category where there was standing water; n=5 for the unsaturated category, where mean 0–0.20 m volumetric water content was 57 %).


When CH4 emissions were greatest in the saturated plots, both REDOX potential and the PRS ion adsorption rates indicated reduced soil conditions (higher Mn2+ and Fe2+ and lower S net adsorption; Fig. 5). Using just the August data from all lowland plots, the LME model indicated that the average net adsorption of Mn2+ was 16.0±3.7µg 10 cm−2 per month higher in saturated conditions and 7.1±2.3µg 10 m−2 per month higher for the deeper (0.2 m) probes. The net adsorption of Fe2+ was 188±36µg 10 m−2 per month higher in saturated conditions, but there was no significant difference at depth (β2=42±24). The net adsorption of S was 588±92µg 10 m−2 per month lower in the saturated plots, but there was no significant difference between the two depths (β2=-74±63). The median REDOX potentials were −127 and −168 mV in the saturated plots at 0.2 and 0.4 m below the surface, respectively. The LME model (Eq. 2) indicated REDOX potentials were 116 mV ± 47 (hydrogen standard) lower in saturated conditions and 85 mV ± 33 lower at a 0.4 m depth (Table 3).

The PCA's leading component related increasing net adsorption rates of NH4+ and the metals with decreasing S. Together, the leading two components of the PCA explained 89.8 % of the variability in net ion adsorption rates for the deep probes (with 79.1 % explained by the first component) for the nine plots with REDOX potential measurements. All ions loaded relatively evenly in magnitude on the leading component (PC1; Table 4), but S was inverse to the others. Although the negative sign of the correlation coefficient between PC1 and the REDOX potential (R=-0.24) intuitively matched what would be expected for a REDOX gradient, where more negative potentials were associated with less S availability and more Mn2+ and Fe2+, it was not significantly different from zero (p=0.243). The correlation coefficient between PC1 and log-transformed CH4 fluxes (R=0.378) was also not significant (p=0.06), perhaps due to relatively few observations at the REDOX monitoring transect in 2015 (n=25). However, the same analysis conducted for all plots' PRS data (n=163) found similar weighting on PC1 and a significant (p<0.001) correlation between PC1 and log-transformed CH4 fluxes (R=0.31). This suggests a link between increasing CH4 emissions and decreasing S and increasing Mn2+, Fe2+, and NH4+ availability. Some of the individual ion adsorption rates were correlated to log-transformed CH4 fluxes for the nine plots along the moisture gradient in the lowland and for the entire data set (Table 5). At the REDOX monitoring transect in 2015, only S adsorption was negatively and significantly correlated to CH4 emissions, but when the full data set was included, CH4 emissions were significantly correlated with the following ion adsorption rates in the following order, by correlation strength: Mn2+=Fe2+>NH4+>NO3- (Table 5). Overall, the correlations were similar for shallow and deep probes (Table 5). A significant correlation was also found between CH4 fluxes and 0–20 cm integrated volumetric soil moisture (R=0.24), whereas no significant relationship was found for 0.02 m soil temperature (R=-0.04).

Table 4PCA loadings and the Pearson correlation for principle components (PC) 1 and 2 and REDOX potential and log-transformed CH4 flux (p values given in parentheses). Methane fluxes were averaged over the same 1-month periods in which the PRS probes were buried. Bold numbers indicate significant correlations at α=0.05, n=25.

Download Print Version | Download XLSX

Table 5Pearson correlation coefficients between natural logarithm-transformed CH4 fluxes and plant root simulator (PRS) ion exchange resin measurements. Methane fluxes were averaged over the same 1-month periods in which the PRS probes were buried, n=25 for transect data and n=163 for the entire study. Deep probes were buried outside the collars at 0.2 m, and shallow probes were buried at 0.1 m outside the collars. Significant correlations (α=0.05) are in bold.

Download Print Version | Download XLSX

5 Discussion

Methane emissions typically increase with increasing saturation/rising water tables within (Moore et al., 2011) and among peatlands (Turetsky et al., 2014), and they also tend to increase when drained peatlands are restored by wetting (Table S1). However, CH4 emissions in the newly constructed SFW unexpectedly remained very low over the first 3 years since wetting, despite abundant vegetation with aerenchymatous tissues, peat soils, and high water tables. Over the 3-year study period, the only plots that showed small but increasing trends in CH4 emissions over time were vegetated plots with standing water above the soil surface. The vegetation at these plots was primarily Carex aquatilis and Typha latifolia. These species have aerenchymatous tissues that enable plant-mediated transport of CH4 to the surface and have been reported in the peatland restoration literature to promote CH4 emissions (Mahmood and Strack, 2011; Wilson et al., 2009).

Median CH4 fluxes from this system are 0.2 % to 50 % of the values published from other studies on rewetted peatlands (Tables 1 and S1). Instead, the fluxes in this study are similar to those reported from the other constructed wetland in the AOSR (median CH4 emissions were below 0.08 mg m−2 h−1) and an undisturbed saline fen (Murray et al., 2017). Murray et al. (2017) accredited the low CH4 emissions and low CH4 pore water concentrations at the constructed wetland to the supply rate of mobile S. Methanogens, CH4-producing microorganisms, are obligate anaerobes, and an abundance of alternative electron acceptors such as SO42- can support microbial communities that can outcompete methanogens. This effect has been described using the conceptual framework of the REDOX “ladder” (for a detailed definition see Bethke et al., 2011). Simply, a conceptual pristine aquifer will contain zones with distinct electron acceptors for metabolic REDOX reactions as reduction potentials decrease (Lovley et al., 1994). The sequence starts with the reduction of oxygen until it is consumed, then oxidized nitrogen (NO3-), oxidized metals (non-mobile MnO2 and Fe(OH)3), S (e.g. SO42-), and finally the production of CH4 through the reduction of CO2 or acetate. In incubation studies, methanogens can be outcompeted by both metal-reducing bacteria (MRB) (Achtnich et al., 1995; Miller et al., 2015) and sulfur-reducing bacteria (SRB) (Achtnich et al., 1995; Akunna et al., 1998; Gauci and Chapman, 2006; Granberg et al., 2001; Hahn-Schöfl et al., 2011; Kang et al., 1998; Kuivila et al., 1989; Lovley and Klug, 1983; Peters and Conrad, 1995; Watson and Nedwell, 1998). Although the community dynamics between MRB, SRB, and methanogens is complex (Bethke et al., 2011), increased interactions among these organisms often lead to the suppression of methanogenic activity since microbial communities are competing for H2 and acetate, which methanogenic microbes require exclusively for their metabolism. In some fen peatlands, drought conditions have been shown to increase alternative electron acceptor abundance and suppress CH4 production after rewetting (Estop-Aragonés et al., 2013). Two lines of evidence suggest that methanogenesis was inhibited in the SFW through this mechanism. Within the plots with REDOX probes, the largest (albeit still very small) CH4 fluxes were observed where reduction potentials at both 0.2 and 0.4 m below the surface were close to hydrogen standards of −200 mV, potentials known to be favourable for methanogenesis (Akunna et al., 1998). At these potentials, the net adsorption of reduced metals (Fe2+ and Mn2+) was the greatest, and mobile S, which would be largely SO42-, was lowest. In those nine plots where REDOX was observed, only S had a significant relationship to CH4, but Fe2+ and Mn2+ were also found to have a significant correlation to CH4 with the full data set. In addition, CH4 emissions and ebullition events increased over time in the saturated plots (those with standing water) throughout the lowland while mobile S appeared to be declining in abundance as the presence of mobile metals (Fe2+ and Mn2+) increased. This suggests the SFW soil became more reduced with a decrease in SRB abundance, which eased the competitive exclusion of methanogenic organisms. This conclusion follows Christiansen et al. (2016), who also found that Fe2+ measured with PRS probes was highest in conditions which promoted greater CH4 emissions.

Wetter soils are expected to increase the probability of mobile ions diffusing toward the PRS probes. For example, Wood et al. (2015) found that the variability of net adsorption rates of Mn2+, Fe2+, and S flux was greatest when the soil volumetric moisture content was highest in three undisturbed wetland sites from the same region as this study. Wood et al. (2015) interpreted these results as an increase in ion availability as well as increased mobility. However, if a change in either availability or mobility was the driving force of the observed variability in this study, all abundant ions should increase (or decrease) as they did in the Wood et al. (2015) study. Here, mobile S fluxes decreased in the saturated soils where reduced metal ions were increasing. The loading of net adsorption rates of S on PC1 was almost equal to the other ions, but was negative (Table 4), suggesting that the leading mode of variability in ion adsorption rates had an opposite relationship between the reduced and oxidized ions. This suggests that microbially mediated REDOX reactions such as those by SRB and MRB are important in the changing biogeochemistry of the SFW peat soils. Negative correlations between time and mobile S and NO3- and positive correlations between time and reduced metals and NH4+ provide additional evidence that alternative electron acceptors are being consumed over time (Table 2). The results presented here are comparable to a study by Kreiling et al. (2015), who found an increase in PRS-adsorbed Mn2+ and Fe2+ along with a decrease in mobile S with increasing flood frequency within the Mississippi River floodplain. They too attributed these changes in ion adsorption to decreasing REDOX potentials.

Although there is evidence that the soil REDOX conditions and alternative electron acceptor abundance vary in time and space at the SFW as described by the REDOX ladder, the variability in CH4 emissions was not strongly explained by these factors. This may be due in part to the complexity associated with electron acceptor abundance and CH4 production. In one study, methanogen communities were documented to become better competitors, relative to MRB, for scarce resources in Arctic tundra soils with increasing temperatures at higher REDOX potentials (Herndon et al., 2015). Granberg et al. (2001) demonstrated that vegetation, rapid temperature shifts, and N and S deposition all had significant dependent effects on CH4 fluxes. In that study, the effects of the interaction terms were as large as, and sometimes inverse to, the effects of each variable correlated to CH4 fluxes alone. Other factors might include the role of humic substances, soil heterogeneity and microsites, salinity, pH, and a breakdown of the REDOX ladder conceptual framework. For example, there is evidence that humic substances can suppress CH4 production, by becoming anaerobic election acceptors (Blodau and Deppe, 2012), and more recently particulate organic matter itself has been shown to be an important electron acceptor in peat soils (Gao et al., 2019). Microsites (<10µm) with limited gas and water exchange with surrounding soil pore space may also affect overall soil REDOX potential and CH4 production by permitting localized electron acceptor depletion or abundance (Sey et al., 2008). Soil salinity may also have impacted the CH4 emissions from this wetland constructed on top of mine tailings; in 2013, the electrical conductivity was 792±616µS cm−1, which increased to 2163±248µS cm−1 in 2015 (Biagi et al., 2019). Although the effects of salinity on CH4 production are not well understood, Poffenbarger et al. (2011) reviewed the literature and found CH4 emissions were suppressed only in polyhaline wetlands (18 g L−1 or ∼24 mS cm−1) where salinity far exceeded that of the SFW. In this constructed wetland the dominant form of cation is Ca2+ not Na+, and thus it is unknown what effect this may have on the microbes at this time. However, Na+ concentrations have been increasing from 56±52 mg L−1 in 2013 to 130±109 mg L−1 in 2015 (Biagi et al., 2019), suggesting a trend towards more common Na+-dominated saline environments. The assemblage of anaerobic microbes that are thermodynamically favoured in a soil also varies with pH since the Gibbs energies of some alternative electron-accepting metabolic process, but not others, vary with hydrogen ion concentration (Bethke et al., 2011; Flynn et al., 2014). Bethke et al. (2011) concluded that at neutral pH, the Gibbs energies of the major metabolic pathways of Fe3+ reduction, SO42- reduction, and methanogenesis all converge. This contradicts the competitive exclusion concept of the REDOX ladder at neutral conditions. Other reactions can also have a cascading effect on the thermodynamics of the system. For example, Kreiling et al. (2015) found that precipitation of Fe2+ and H2PO4- leads to non-linear trends in Fe2+ ion adsorption to ion exchange resins despite increasing time in anoxic conditions. Kreiling et al. (2015) demonstrated that the precipitate removed waste products and maintained the system's relative abundance of oxidized iron (Fe3+), thereby maintaining forward reactions within Fe-reducing metabolic pathways. Currently, microsite conditions are very difficult to assess at the level Bethke et al. (2011) argue is needed to explain anaerobic microbial community dynamics on a thermodynamic basis.

At the SFW, it is reasonable to assume that N and S deposition near an oil sand processing plant could influence soil biogeochemistry and the results described here. Even before wetting, high concentrations of total S and available S in the peat used to construct the SFW were similar to an undisturbed fen in Alberta as reported by Chagué-Goff et al. (1996). Such high concentrations of S occur when the groundwater that supplies the fen passes though coal and dark shale deposits. Because Alberta is rich in both types of deposits, fens classified as “moderate rich” or “extreme rich” in terms of ion abundance, such as the four boreal fens described by Hartsock et al. (2016), are not uncommon in the region. High concentrations of S are also found in natural tidal wetlands where CH4 emissions are typically low (Poffenbarger et al., 2011). However, due to the abrupt change in environmental conditions affecting the salvaged peat with placement and flooding in the SFW, the mobile S appears to be declining in abundance in the anoxic regions of this system. In the future, surface soil SO42- may be replenished by diffusion from the underlying tailings, which has high concentrations of gypsum added during post-processing to promote aggregation of soft tailings (Oil Sands Wetland Working Group, 2014). However, there is no indication that the upward vertical transport of salts from the tailing sands is occurring at a rate to offset the current decline in mobile S (Biagi et al., 2019). Therefore, without any other processes limiting production, CH4 emissions may increase in the future at the SFW.

6 Conclusions

Carbon cycling processes in constructed boreal plains lowlands are not yet well understood as these ecosystems have only existed for a few years. This study shows that CH4 emissions are very low in the SFW, one of the first of two boreal plains lowlands constructed in boreal northern Alberta. Methane emissions were low compared to rewetted and restored peatlands but similar to another newly constructed wetland in the Alberta oil sand region. Changes in ion adsorption rates on buried ion exchange resins (PRS probes) were related to decreasing REDOX potentials and were used to support the argument that methanogen activity may be competitively suppressed by an abundance of alternative electron acceptors. Seasonal and interannual variations in net ion adsorption rates suggest microbially mediated changes in soil chemistry. In particular, decreases in PRS S adsorption occur concurrently with modest increases in CH4 emissions in the lowlands of the SFW, suggesting CH4 emissions are likely to increase in the future, if the trends in the abundance of electron acceptors continue. The findings of this research indicate that the design of the SFW promotes, at least initially, highly reduced soils in the lowlands with limited CH4 production. This is significant as the REDOX conditions necessary for long-term C accumulation appear to be achieved while limiting the emissions of a potent greenhouse gas.

Data availability

Data will be provided on request.


The supplement related to this article is available online at:

Author contributions

Funding was obtained by ERH and SKC, who also supervised MGC during this work. The experiments were designed by MGC and ERH, with MGC conducting them in the field. This paper was written by MGC, who also performed the primary investigation, with contributions from all co-authors.

Competing interests

This work was funded by an industrial partner in the oil and gas sector of Canada.


We thank everyone who helped with the fieldwork, Erin Nicholls, Kelly Biagi, Haley Spennato, Chelsea Thorne, Jessica Sara, Arthur Szybalski, Gord Drewitt, and Mike Treberg for building and helping maintain the gas exchange chambers. We would also like to thank the dedicated team at the Reclamation and Closure Department of Syncrude Canada for their support.

Financial support

This research has been supported by Syncrude Canada Ltd. (grant no. 441022033).

Review statement

This paper was edited by Tina Treude and reviewed by one anonymous referee.


Achtnich, C., Bak, F., and Conrad, R.: Competition for electron donors among nitrate reducers, ferric iron reducers, sulfate reducers, and methanogens in anoxic paddy soil, Biol. Fert. Soils, 19, 65–72, 1995. 

Akunna, J. C., Bernet, N., and Moletta, R.: Effect of nitrate on methanogenesis at low redox potential, Environ. Technol., 19, 1249–1254, 1998. 

Alberta Government: Alberta's leased oil sands area map, available at: (last access: 3 July 2019), 2017. 

Beetz, S., Liebersbach, H., Glatzel, S., Jurasinski, G., Buczko, U., and Höper, H.: Effects of land use intensity on the full greenhouse gas balance in an Atlantic peat bog, Biogeosciences, 10, 1067–1082,, 2013. 

Beilman, D. W., Vitt, D. H., Bhatti, J. S., and Forest, S.: Peat carbon stocks in the southern Mackenzie River Basin: Uncertainties revealed in a high-resolution case study, Glob. Change Biol., 14, 1221–1232, 2008. 

Bethke, C. M., Sanford, R. A., Kirk, M. F., Jin, Q., and Flynn, T. M.: The thermodynamic ladder in geomicrobiology, Am. J. Sci., 311, 183–210, 2011. 

Biagi, K. M., Oswald, C. J., Nicholls, E. M., and Carey, S. K.: Increases in salinity following a shift in hydrologic regime in a constructed wetland watershed in a post-mining oil sands landscape, Sci. Total Environ., 653, 1445–1457, 2019. 

Blodau, C. and Deppe, M.: Humic acid addition lowers methane release in peats of the Mer Bleue bog, Canada, Soil Biol. Biochem., 52, 96–98, 2012. 

Blossfeld, S., Gansert, D., Thiele, B., Kuhn, A. J., and Lösch, R.: The dynamics of oxygen concentration, pH value, and organic acids in the rhizosphere of Juncus spp., Soil Biol. Biochem., 43, 1186–1197, 2011. 

Bousquet, P., Ciais, P., Miller, J. B., Dlugokencky, E. J., Hauglustaine, D. A., Prigent, C., Van der Werf, G. R., Peylin, P., Brunke, E.-G., Carouge, C., Langenfelds, R. L., Lathière, J., Papa, F., Ramonet, M., Schmidt, M., Steele, L. P., Tyler, S. C., and White, J.: Contribution of anthropogenic and natural sources to atmospheric methane variability, Nature, 443, 439–443, 2006. 

Bubier, J., Moore, T., Savage, K., and Crill, P.: A comparison of methane flux in a boreal landscape between a dry and a wet year, Global Biogeochem. Cy., 19, 1–11, 2005. 

Bubier, J. L. and Moore, T. R.: An ecological perspective on methane emissions from northern wetlands, Trends Ecol. Evol., 9, 460–464, 1994. 

Chagué-Goff, C., Goodarzi, F., and Fyfe, W. S.: Elemental distribution and pyrite occurrence in a freshwater peatland, Alberta, J. Geol., 104, 649–663, 1996. 

Christen, A., Jassal, R. S., Black, T. A., Grant, N. J., Hawthorne, I., Johnson, M. S., Lee, S.-C., and Merkens, M.: Summertime greenhouse gas fluxes from an urban bog undergoing restoration through rewetting, Mires Peat, 17, 1–24, 2016. 

Christiansen, J. R., Levy-Booth, D. J., Prescott, C. E., and Grayston, S. J.: Microbial and environmental controls of methane fluxes along a soil moisture gradient in a Pacific coastal temperate rainforest, Ecosystems, 19, 1255–1270, 2016. 

Clark, M. G., Humphreys, E., and Carey, S. K.: The initial three years of carbon dioxide exchange between the atmosphere and a reclaimed oil sand wetland, Ecol. Eng., 135, 116–126, 2019. 

Couwenberg, J.: Methane emissions from peat soils (organic soils, histosols) facts, MRV-ability, emission factors, Wetlands International, Wageningen, the Netherlands, 2009. 

Dacey, J. W. H., Drake, B. G., and Klug, M. J.: Stimulation of methane emission by carbon dioxide enrichment of marsh vegetation, Nature, 370, 47–49, 1994. 

Ding, W., Cai, Z., and Tsuruta, H.: Plant species effects on methane emissions from freshwater marshes, Atmos. Environ., 39, 3199–3207, 2005. 

Environment and Climate Change Canada: Fort McMurray A Climate Normals, available at:, last access: 26 August 2016. 

Environmental Protection and Enhancement Act: Province of Alberta, available at:, last access: 6 June 2017. 

Estop-Aragonés, C., Knorr, K.-H., and Blodau, C.: Belowground in situ redox dynamics and methanogenesis recovery in a degraded fen during dry-wet cycles and flooding, Biogeosciences, 10, 421–436,, 2013. 

Flynn, T. M., O'Loughlin, E. J., Mishra, B., DiChristina, T. J., and Kemner, K. M.: Sulfur-mediated electron shuttling during bacterial iron reduction, Science, 344, 1039–1042, 2014. 

Gao, C., Sander, M., Agethen, S., and Knorr, K.-H.: Electron accepting capacity of dissolved and particulate organic matter control CO2 and CH4 formation in peat soils, Geochim. Cosmochim. Ac., 245, 266–277, 2019. 

Gauci, V. and Chapman, S. J.: Simultaneous inhibition of CH4 efflux and stimulation of sulphate reduction in peat subject to simulated acid rain, Soil Biol. Biochem., 38, 3506–3510, 2006. 

Geer, K. G. and Schoenau, J. J.: Salinity and salt contamination assessment using anion exchange resin membranes, in: Soils and Crops Workshop Proceedings, Univ. Saskatchewan, Saskatoon, AB, Canada, 44–48, 1994. 

Granberg, G., Sundh, I., Svensson, H., and Nilsson, M.: Effects of temperature and nitrogen and sulfur deposition on methane emission from a boreal mire, Ecology, 82, 1982–1998, 2001. 

Hahn-Schöfl, M., Zak, D., Minke, M., Gelbrecht, J., Augustin, J., and Freibauer, A.: Organic sediment formed during inundation of a degraded fen grassland emits large fluxes of CH4 and CO2, Biogeosciences, 8, 1539–1550,, 2011. 

Harrison, D. J. and Maynard, D. G.: Nitrogen mineralization assessment using PRS™ probes (ion-exchange membranes) and soil extractions in fertilized and unfertilized pine and spruce soils, Can. J. Soil Sci., 94, 21–34, 2014. 

Hartsock, J. A., House, M., and Vitt, D. H.: Net nitrogen mineralization in boreal fens?: a potential performance indicator for peatland reclamation, Botany, 94, 1027–1040, 2016. 

Herndon, E. M., Mann, B. F., Roy Chowdhury, T., Yang, Z., Wullschleger, S. D., Graham, D., Liang, L., and Gu, B.: Pathways of anaerobic organic matter decomposition in tundra soils from Barrow, Alaska, J. Geophys. Res.-Biogeo., 120, 2345–2359, 2015. 

Hutchinson, G. L. and Livingston, G. P.: Vents and seals in non-steady-state chambers used for measuring gas exchange between soil and the atmosphere, Eur. J. Soil Sci., 52, 675–682, 2001. 

IPCC: Climate Change 2013: The physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change, edited by: Stocker, T. F., Qin, D., Plattner, G.-K., Tignor, M., Allen, S. K., Boschung, J., Nauels, A., Xia, Y., Bex, V., and Midgley, P. M., Cambridge University Press, Cambridge, UK and New York, NY, USA, 1535 pp., 2013. 

IPCC (Blain, D., Murdiyarso, D., Couwenberg, J., Nagata, O., Renou-Wilson, F., Sirin, A., Strack, M., Tuittila, E.-S., Wilson, D., Evans, C. D., Fukuda, M., and Parish, F.): Rewetted organic soils, in: 2013 Supplement to the 2006 IPCC guidelines for national greenhouse gas inventories: wetlands, edited by: Hiraishi, T., Krug, T., Tanabe, K., Srivastava, N., Jamsranjav, B., Fukuda, M., and Troxler, T., IPCC, Switzerland, 3.1–3.43, 2014. 

Juottonen, H., Hynninen, A., Nieminen, M., Tuomivirta, T. T., Tuittila, E., Nousiainen, H., and Kell, D. K.: Methane-cycling microbial communities and methane emission in natural and restored peatlands, Appl. Environ. Microb., 78, 6386–6389, 2012. 

Kang, H., Freeman, C., and Lock, M. A.: Trace gas emissions from a north wales fen – role of hydrochemistry and soil enzymore activity, Water Air Soil Poll., 105, 107–116, 1998. 

Kim, D.-G., Vargas, R., Bond-Lamberty, B., and Turetsky, M. R.: Effects of soil rewetting and thawing on soil gas fluxes: a review of current literature and suggestions for future research, Biogeosciences, 9, 2459–2483,, 2012. 

Kirschke, S., Bousquet, P., Ciais, P., Saunois, M., Canadell, J. G., Dlugokencky, E. J., Bergamaschi, P., Bergmann, D., Blake, D. R., Bruhwiler, L., Cameron-Smith, P., Castaldi, S., Chevallier, F., Feng, L., Fraser, A., Heimann, M., Hodson, E. L., Houweling, S., Josse, B., Fraser, P. J., Krummel, P. B., Lamarque, J.-F., Langenfelds, R. L., Le Quéré, C., Naik, V., O'Doherty, S., Palmer, P. I., Pison, I., Plummer, D., Poulter, B., Prinn, R. G., Rigby, M., Ringeval, B., Santini, M., Schmidt, M., Shindell, D. T., Simpson, I. J., Spahni, R., Steele, L. P., Strode, S. A., Sudo, K., Szopa, S., van der Werf, G. R., Voulgarakis, A., van Weele, M., Weiss, R. F., Williams, J. E., and Zeng, G.: Three decades of global methane sources and sinks, Nat. Geosci., 6, 813–823, 2013. 

Kludze, H. K., DeLaune, R. D., and Patrick, W. H.: Aerenchyma formation and methane and oxygen exchange in rice, Soil Sci. Soc. Am. J., 57, 386–391, 1993. 

Kreiling, R. M., De Jager, N. R., Swanson, W., Strauss, E. A., and Thomsen, M.: Effects of flooding on ion exchange rates in an Upper Mississippi River floodplain forest impacted by herbivory, invasion, and restoration, Wetlands, 35, 1005–1012, 2015. 

Kuivila, K. M., Murray, J. W., Devol, A. H., and Novelli, P. C.: Methane production, sulfate reduction and competition for substrates in the sediments of Lake Washington, Geochim. Cosmochim. Ac., 53, 409–416, 1989. 

Lai, D. Y. F., Roulet, N. T., Humphreys, E. R., Moore, T. R., and Dalva, M.: The effect of atmospheric turbulence and chamber deployment period on autochamber CO2 and CH4 flux measurements in an ombrotrophic peatland, Biogeosciences, 9, 3305–3322,, 2012. 

Le Mer, J. and Roger, P.: Production, oxidation, emission and consumption of methane by soils: A review, Eur. J. Soil Biol., 37, 25–50, 2001. 

Li, S., Lin, B., and Zhou, W.: Soil sulfur supply assessment using anion exchange resin strip-plant root simulator probe, Commun. Soil Sci. Plan., 32, 711–722, 2001. 

Limpens, J., Berendse, F., Blodau, C., Canadell, J. G., Freeman, C., Holden, J., Roulet, N., Rydin, H., and Schaepman-Strub, G.: Peatlands and the carbon cycle: from local processes to global implications – a synthesis, Biogeosciences, 5, 1475–1491,, 2008. 

Lovley, D. R. and Klug, M. J.: Sulfate reducers can outcompete methanogens at freshwater sulfate concentrations, Appl. Environ. Microb., 45, 187–192, 1983. 

Lovley, D. R., Chapelle, F. H., and Woodward, J. C.: Use of dissolved H2 concentrations to determine distribution of microbially catalyzed redox reactions in anoxic groundwater, Environ. Sci. Technol., 28, 1205–1210, 1994. 

Mahmood, M. S. and Strack, M.: Methane dynamics of recolonized cutover minerotrophic peatland: Implications for restoration, Ecol. Eng., 37, 1859–1868, 2011. 

Megonigal, J. P. and Schlesinger, W. H.: Enhanced CH4 emissions from a wetland soil exposed to elevated CO2, Biogeochemistry, 37, 77–88, 1997. 

Miller, K. E., Lai, C. T., Friedman, E. S., Angenent, L. T., and Lipson, D. A.: Methane suppression by iron and humic acids in soils of the Arctic Coastal Plain, Soil Biol. Biochem., 83, 176–183, 2015. 

Moore, T. R., Roulet, N. T., and Waddington, J. M.: Uncertainty in predicting the effects of climatic change on the carbon cyling of Canadian peatlands, Climatic Change, 40, 229–245, 1998. 

Moore, T. R., De Young, A., Bubier, J. L., Humphreys, E. R., Lafleur, P. M., and Roulet, N. T.: A multi-year record of methane flux at the Mer Bleue Bog, southern Canada, Ecosystems, 14, 646–657, 2011. 

Murray, K. R., Barlow, N., and Strack, M.: Methane emissions dynamics from a constructed fen and reference sites in the Athabasca Oil Sands Region, Alberta, Sci. Total Environ., 583, 369–381, 2017. 

Nicholls, E., Carey, S., Humphreys, E. R., Clark, M. G., and Drewitt, G.: Multi-year water balance assessment of a newly constructed wetland, Fort McMurray, Alberta, Hydrol. Process., 30, 2739–2753, 2016. 

Nwaishi, F., Petrone, R. M., Price, J. S., and Andersen, R.: Towards developing a functional-based approach for constructed peatlands evaluation in the Alberta oil sands region, Canada, Wetlands, 35, 211–225, 2015. 

Oil Sands Wetland Working Group: Guideline for wetland establishment on reclaimed oil sands leases, Cumulative Environmental Management Association, 3rd Edn., available at: (last access: 3 July 2019), 2014. 

Oswald, C. J. and Carey, S. K.: Total and methyl mercury concentrations in sediment and water of a constructed wetland in the Athabasca Oil Sands Region, Environ. Pollut., 213, 628–637, 2016. 

Parkin, T. B. and Venterea, R. T.: USDA-ARS GRACEnet project protocols, chap. 3, Chamber-based trace gas flux measurements, Sampling Protocols, Beltsville, MD, 1–39, 2010. 

Peters, V. and Conrad, R.: Sequential reduction processes and initiation of CH4 production upon flooding of oxic upland soils, Soil Biol. Biochem., 28, 371–382, 1995. 

Poffenbarger, H. J., Needelman, B. A., and Megonigal, J. P.: Salinity influence on methane emissions from tidal marshes, Wetlands, 31, 831–842, 2011. 

Qian, P. and Schoenau, J. J.: Use of ion-exchange membrane to assess nitrogen-supply power of soils, J. Plant Nutr., 28, 2193–2200, 2005. 

Qian, P., Schoenau, J. J., and Huang, W. Z.: Use of Ion exhange membranes in routine soil testing, Commun. Soil Sci. Plan., 23, 1791–1804, 1992. 

Qian, P., Schoenau, J. J., and Ziadi, N.: Ion supply rates using ion-exchange resins, in: Soil Sampling and Methods of Analysis, edited by: Carter, M. R. and Gregorich, E. G., CRC Press, Boca Raton, FL, 161–166, 2008. 

Rochefort, L. and Lode, E.: Restoration of degraded boreal peatlands, in: Boreal Peatland Ecosystems, edited by: Wieder, R. K. and Vitt, D. H., Springer, Berlin, 382–423, 2006. 

Rooney, R. C., Bayley, S. E., and Schindler, D. W.: Oil sands mining and reclamation cause massive loss of peatland and stored carbon, P. Natl. Acad. Sci. USA, 109, 4933–4937, 2012. 

Roulet, N. T., Moore, T. R., Bubier, J. L., and Lafleur, P. M.: Northern fens: methane flux and climate change, Tellus B, 44, 100–105, 1992. 

Rydin, H. and Jeglum, J. K.: The Biology of Peatlands, Oxford University Press, Oxford, p. 250, 2006. 

Sey, B. K., Manceur, A. M., Whalen, J. K., Gregorich, E. G., and Rochette, P.: Small-scale heterogeneity in carbon dioxide, nitrous oxide and methane production from aggregates of a cultivated sandy-loam soil, Soil Biol. Biochem., 40, 2468–2473, 2008. 

Thomas, C. R., Miao, S., and Sindhoj, E.: Environmental factors affecting temporal and spatial patterns of soil redox potential in Florida Everglades wetlands, Wetlands, 29, 1133–1145, 2009. 

Tokida, T., Miyazaki, T., Mizoguchi, M., Nagata, O., Takakai, F., Kagemoto, A., and Hatano, R.: Falling atmospheric pressure as a trigger for methane ebullition from peatland, Global Biogeochem. Cy., 21, 1–8, 2007. 

Trites, M. and Bayley, S. E.: Vegetation communities in continental boreal wetlands along a salinity gradient: Implications for oil sands mining reclamation, Aquat. Bot., 91, 27–39, 2009. 

Turetsky, M. R., Kotowska, A., Bubier, J., Dise, N. B., Crill, P., Hornibrook, E. R. C., Minkkinen, K., Moore, T. R., Myers-Smith, I. H., Nykänen, H., Olefeldt, D., Rinne, J., Saarnio, S., Shurpali, N., Tuittila, E. S., Waddington, J. M., White, J. R., Wickland, K. P., and Wilmking, M.: A synthesis of methane emissions from 71 northern, temperate, and subtropical wetlands, Glob. Change Biol., 20, 2183–2197, 2014. 

Urbanová, Z., Picek, T., Hájek, T., and Bufková, I.: Vegetation and carbon gas dynamics under a changed hydrological regime in central European peatlands, Plant Ecol. Divers., 5, 89–103, 2012. 

Vann, C. D. and Megonigal, J. P.: Elevated CO2 and water depth regulation of methane emissions: Comparison of woody and non-woody wetland plant species, Biogeochemistry, 63, 117–134, 2003. 

Vasander, H. and Kettunen, A.: Carbon in boreal peatlands, Boreal Peatl. Ecosyst., 188, 165–194, 2006. 

Vitt, D. H., House, M., and Hartsock, J. A.: Sandhill Fen, An initial trial for wetland species assembly on in-pit substrates: lessons after three years, Botany, 94, 1–33, 2016. 

Vorenhout, M., van der Geest, H. G., and Hunting, E. R.: An improved datalogger and novel probes for continuous redox measurements in wetlands, Int. J. Environ. An. Ch., 91, 801–810, 2011. 

Waddington, J. M. and Day, S. M.: Methane emissions from a peatland following restoration, J. Geophys. Res., 112, 1–11, 2007. 

Watson, A. and Nedwell, D. B.: Methane production and emission from peat: the influence of anions (sulphate, nitrate) from acid rain, Atmos. Environ., 32, 3239–3245, 1998. 

Whalen, S. C.: Biogeochemistry of methane exchange between natural wetlands and the atmosphere, Environ. Eng. Sci., 22, 73–94, 2005. 

Whiting, G. J. and Chanton, J. P.: Primary production control of methane emission from wetlands, Nature, 364, 794–795, 1993. 

Wilson, D., Alm, J., Laine, J., Byrne, K. A., Farrell, E. P., and Tuittila, E. S.: Rewetting of cutaway peatlands: Are we re-creating hot spots of methane emissions?, Restor. Ecol., 17, 796–806, 2009. 

Wilson, D., Blain, D., Couwenberg, J., Evans, C. D., Murdiyarso, D., Page, S. E., Renou-Wilson, F., Rieley, J. O., Sirin, A., Strack, M., and Tuittila, E.-S.: Greenhouse gas emission factors associated with rewetting of organic soils, Mires Peat, 17, 1–28, 2016.  

Wilson, K. S. and Humphreys, E. R.: Carbon dioxide and methane fluxes from Arctic mudboils, Can. J. Soil Sci., 90, 441–449, 2010. 

Wood, M. E., Macrae, M. L., Strack, M., Price, J. S., Osko, T. J., and Petrone, R. M.: Spatial variation in nutrient dynamics among five different peatland types in the Alberta oil sands region, Ecohydrology, 9, 688–699, 2015. 

Wytrykush, C., Vitt, D., McKenna, G., and Vassov, R.: Designing landscapes to support peatland development on soft tailings deposits, in: Resotration and Reclamation of Breal Ecosystem, edited by: Vitt, D. H. and Bhatti, J., Cambridge University Press, 161–178, 2012. 

Yu, L., Huang, Y., Zhang, W., Li, T., and Sun, W.: Methane uptake in global forest and grassland soils from 1981 to 2010, Sci. Total Environ., 607, 1163–1172, 2017. 

Ziska, L. H., Moya, T. B., Wassmann, R., Namuco, O. S., Lantin, R. S., Aduna, J. B., Abao, E., Bronson, K. F., Neue, H. U., and Olszyk, D.: Long-term growth at elevated carbon dioxide stimulates methane emission in tropical paddy rice, Glob. Change Biol., 4, 657–665, 1998. 

Short summary
Natural and restored wetlands typically emit methane to the atmosphere. However, we found that a wetland constructed after oil sand mining in boreal Canada using organic soils from local peatlands had negligible emissions of methane in its first 3 years. Methane production was likely suppressed due to an abundance of alternate inorganic electron acceptors. Methane emissions may increase in the future if the alternate electron acceptors continue to decrease.
Final-revised paper