Toward a statistical description of methane emissions from arctic wetlands
Methane (CH4) emissions from arctic tundra typically follow relations with soil temperature and water table depth, but these process-based descriptions can be difficult to apply to areas where no measurements exist. We formulated a description of the broader temporal flux pattern in the growing season based on two distinct CH4 source components from slow and fast-turnover carbon. We used automatic closed chamber flux measurements from NE Greenland (74°N), W Greenland (64°N), and Svalbard (78°N) to identify and discuss these components. The temporal separation was well-suited in NE Greenland, where the hypothesized slow-turnover carbon peaked at a time significantly related to the timing of snowmelt. The temporally wider component from fast-turnover carbon dominated the emissions in W Greenland and Svalbard. Altogether, we found no dependence of the total seasonal CH4 budget to the timing of snowmelt, and warmer sites and years tended to yield higher CH4 emissions.
KeywordsEmission Greenland Methane Svalbard Tundra
The small coverage of measurement sites in arctic tundra causes large uncertainties in regional emission budgets of the greenhouse gas methane (CH4) (McGuire et al. 2012). The process-based upscaling of CH4 flux measurements requires detailed information about the local ground conditions (Davidson et al. 2016), which typically cannot be obtained with remote sensing techniques. Arctic tundra ecosystems are predicted to warm and change significantly in the near future (Johannessen et al. 2004; Callaghan et al. 2011a; Cohen et al. 2012), so there are pressing questions about the CH4 flux response to, e.g., earlier snowmelt and generally warmer growing seasons (Callaghan et al. 2011b). Temperature and water table position are often identified as key controls for the short-term CH4 fluxes (Turetsky et al. 2008, 2014; Tagesson et al. 2013), but longer-term seasonal patterns could relate more to the decomposability of the different pools of organic substrates and the development of plants (Christensen et al. 2003; Whalen 2005). So would an earlier snowmelt, causing a longer growing season, lead to larger seasonal emissions? If so, the potentially increased CH4 concentrations in the atmosphere could further amplify climate change effects.
Gas exchange measurements in the Arctic are challenging due to the harsh weather and logistical constraints. The used measurement techniques can also differ tremendously between sites (e.g., Crill et al. 1988; Wagner et al. 2003; Corradi et al. 2005; Parmentier et al. 2011), which complicates inter-site comparisons. The closed chamber technique has proven to be a robust method for CH4 flux measurements, but it is generally not applied continuously throughout the whole growing season (Olefeldt et al. 2013). In the larger framework of the Greenland Ecosystem Monitoring Program, three arctic sites were therefore equipped with the same automatic closed chamber system to continuously monitor CH4 fluxes on the same plots over many growing seasons and the subsequent freeze-in periods. The collected dataset gives unique possibilities to analyze the seasonal patterns at these different ecosystems. The first five years from one of the high-arctic sites (Zackenberg) were previously analyzed by Mastepanov et al. (2013). The derived flux pattern led the authors to hypothesize a bi-component origin of growing season CH4 emissions, driven by two different mechanisms related to slow and fast carbon turnover (Chanton et al. 1995). Accordingly, a first emission peak stems from the slow-turnover carbon of frost-damaged roots or cells of soil microorganisms (Skogland et al. 1988). As methane production from this carbon pool diminishes during the first months after snowmelt, the fast-turnover emissions from root exudates start to dominate the total emissions. This second component leads to a wide peak in the middle of the growing season that is related to the maturity of vascular plants and their root exudates (Ström et al. 2003). Similar interplays of the methanogenic carbon pools have been inferred from measurements in Canadian wetlands (Lai et al. 2014), and matching seasonal patterns have also been measured at Alaskan wetlands (Zona et al. 2016). Mastepanov et al. (2013) additionally reported a third component at the Zackenberg site during the autumnal freeze-in period. This final component is, however, most likely related to physical releases of stored gases in the soil rather than instantaneous methane production (Mastepanov et al. 2008; Pirk et al. 2015).
The formation and emission of CH4 can be studied using process-based models (Zhuang et al. 2004) or measurements of stable isotopic signatures (Hodgkins et al. 2015). The present study follows a different approach using a temporal separation of the flux time series to investigate the bi-component source pattern. We apply the method to measurements from three arctic sites located across a gradient from the low Arctic (central W Greenland) to the high Arctic (NE Greenland and Svalbard), and relate the resulting flux patterns to site differences of snow cover and ground thermal regime. Finally, we compare the total seasonal CH4 emissions with the length of the snow-free period and its overall temperature.
Materials and methods
The site in Zackenberg Valley (74°30′N, 21°00′W) in the Northeast Greenland National Park lies in a high-arctic region with a mean annual air temperature of −9.9 °C (1958–1987), continuous permafrost, and a total annual precipitation of 286 mm on average (Hansen et al. 2008). Maximum snow depths vary interannually between 13 and 133 cm (Pedersen et al. 2016). The measurement site is located on the edge of a fen, on a large alluvial fan, whose vegetation is dominated by Eriophorum scheuchzeri, Carex cf. stans, Dupontia psilosantha, and moss species.
The Kobbefjord site (64°08′N, 52°23′W) in the Nuuk area in Western Greenland lies in a low-arctic fen, featuring a mean annual air temperature of −1.4 °C (1961–1990), no permafrost, and a total annual precipitation of about 750 mm (Cappelen 2013). Maximum snow depths in our measurement period varied between 120 and 150 cm interannually. The fen’s vegetation is dominated by Scirpus caespitosus and E. angustifolium (Bay et al. 2008).
The three field sites are equipped with the same automatic chamber system based on Goulden and Crill (1997). A set of transparent chambers—each covering a square of 60 by 60 cm, with a height of 30 cm—are placed in close proximity to each other at each site. Kobbefjord and Adventdalen each have six chambers. The transect of six chambers at Zackenberg was extended by four additional chambers in 2011, so the most recent years feature ten instead of six chambers. Inside each chamber a fan ensures ventilation and gas mixing. High-density polyethylene tubes connect each chamber to the CH4 analyzer (Los Gatos Research, USA), which records CH4 concentrations at a rate of 1.0 Hz. The computer running these automatic measurements activates the chambers in succession for 10 min. During the first 3 min, the chamber is open for ventilation, and then closed for 5 min, and opened again for the last 2 min. Each chamber is activated once per cycle while the inactive chambers remain open. The flux calculation is based on ordinary least-squares regression as described by Pirk et al. (2016). This measurement setup yields CH4 flux time series with a resolution of 1 h from each chamber (2 h at Zackenberg after 2011). Our measurements typically start around the time of snowmelt and extend into the freeze-in period as long as the snow conditions allowed (typically covering June through October). Our dataset comprised 8 years of data from Zackenberg (2006–2015), 4 years from Kobbefjord (2012–2015), and 3 years from Adventdalen (2013–2015).
At Kobbefjord and Adventdalen, we used surface albedo measurements from a net radiometer in the direct vicinity of the chambers to determine the day of snowmelt. This day was defined as the first day with an average albedo of less than 0.3, which is a value typically matching our visual assessment. At Zackenberg, where there are no albedo measurements at the chambers, the day of snowmelt was determined by visual inspection on site when most snow had melted inside and around the chambers.
To further characterize each year, we calculated growing degree days (GDD) from daily minimum and maximum air temperatures (T) recorded by a nearby weather station. We used GDD = max (0, (Tmin + Tmax)/2 − Tbase), with base temperature Tbase = 0 °C.
The CH4 flux time series from each individual chamber was temporally separated into three components using the statistical mixing model technique. Two components of this temporal separation are intended to describe the different CH4 growing season sources hypothesized by Mastepanov et al. (2013), while the third component can capture potential autumn bursts (Mastepanov et al. 2008). This model used three Gaussian functions (each with three parameters, i.e., center position, width, and height) whose sum was optimized against the measured fluxes. We used the PyMix software package to estimate these parameters through the standard expectation–maximization algorithm which finds a maximum likelihood solution (Georgi et al. 2010). To reduce higher frequency variations and noise, daily medians of the measured fluxes were calculated first. The temporal separation was then applied from the first to the last day of measurements, between which potential measurement gaps were linearly interpolated. At Zackenberg and Kobbefjord, the data coverage of the daily flux time series was typically above 80%, while at Adventdalen about 50% of the time series needed to be gap-filled.
The seasonal components suggested by the Zackenberg fluxes are not equally well detectable at Kobbefjord and Adventdalen. At Kobbefjord, the model found the components at sometimes quite different positions for each chamber (cf. Fig. 4d). At Adventdalen, the flux time series featured no distinct peaks to constrain the temporal separation model during the growing season (cf. Fig. 4f). Still, the mathematical description by the temporal separation captures the overall pattern of fluxes and the NRMSE is quite comparable to Zackenberg. Our temporal separation model is designed to use all three components to describe the measured fluxes. At Kobbefjord, however, component C cannot be mechanistically associated with the same processes as at the other two sites, because the flux measurements never continued into the autumnal freeze-in period. Besides, no permafrost is present, which is the hypothesized requirement for an autumn burst (Mastepanov et al. 2013).
We used the hypothesized bi-component origin of CH4 emissions in relation to the timing of snowmelt to describe flux patterns at different arctic tundra sites. Finding the statistical distributions of the seasonal flux patterns using only the day of snowmelt is useful to explore site differences and potentially upscale fluxes to areas where no measurements exist. The underlying hypothesis based on slow and fast-turnover carbon could not be tested with our dataset, so alternative explanations remain possible. For example, CH4 fluxes could originate from one dominating source, and surface fluxes could primarily be a result of the seasonal patterns of soil temperature and water table rather than differences in substrate. The sharp rise of emissions after snowmelt at Zackenberg could also stem from stored organic acids or gases that were produced in the previous summer. Many such mechanisms could, however, still be captured with the temporal separation model proposed here or a variation thereof. Therefore, even when the underlying drivers are different, our statistical breakdown would remain useful to describe spatial and temporal patterns in CH4 fluxes. While Mastepanov et al. (2013) treated individual chambers as replicates and derived the flux pattern from mean values and standard deviations, the present study analyzed each chamber individually using a temporal separation into three-components. The choice of Gaussian functions for each component was intended to give a simple description with a minimal number of fitting parameters, so the model did not explicitly represent the mechanisms underlying the suggested hypothesis. Therefore, this model may not resolve the exact shape and integral of the individual seasonal components, as indicated by the mismatches seen in Fig. 2. However, the model’s simplicity leads to numerically robust and intuitive results with three clearly distinguished peaks, which allowed us to investigate the peak center positions at Zackenberg. The results indicate a significant dependence between the timing of the first peak (component A) and day of snowmelt with an average lag of 31.4 days, supporting the findings by Mastepanov et al. (2013). The timing of the second peak (component B)—hypothesized to stem from root exudates of plants—was independent of the day of snowmelt. The center of component B occurred between approximately DOY 210 and 240 (cf. Fig. 3b), which coincides with the typical time of maximum CO2 uptake fluxes in this wetland (Nordstroem et al. 2001; Mastepanov et al. 2013). This match further supports the bi-component hypothesis, because root exudates are expected to correlate with plant growth as measured by CO2 fluxes (Ström et al. 2003). In a nearby heath ecosystem, the plant dynamics later in the growing season have been shown to depend more on incoming sunlight than the timing of snowmelt (Lund et al. 2012). Therefore, a strong dependence between component B and the day of snowmelt is not expected, which follows our hypothesis. After confirming the earlier findings at the Zackenberg site, the same analysis was performed on data from the two sites at Kobbefjord and Adventdalen. The fluxes at these sites, however, showed no clear presence of three seasonal components, so a correlation of the first component with the date of snowmelt did not exist. These differences between the three sites suggest quite different dominating processes behind the CH4 emissions. At Kobbefjord, for example, the growing season CH4 flux has one strongly expressed component (cf. Fig. 4d), which bears a resemblance to component B because of its large width. This site features no permafrost, so despite the seasonal ground freezing, the physical mechanisms proposed to lie behind the autumn CH4 burst cannot be at work (Mastepanov et al. 2008, 2013; Pirk et al. 2015). However, we cannot fully exclude the presence of this flux component at Kobbefjord, because our measurements never continued long enough into the freeze-in period (November–December). Component A might well be present at this site, but could be masked by a shoulder of the much larger component B. The dominance of the component B would be in line with the finding that the total growing season CH4 emission at Kobbefjord appears linearly related to the total growing degree days per season (cf. Fig. 5b). At Zackenberg, in contrast, this relation cannot be seen, possibly because component A is much more pronounced than it is at Kobbefjord.
At Adventdalen, where permafrost is present, the CH4 autumn burst (flux component C) was observed, as suggested by the physical mechanism. Similar autumnal flux patterns with significant contributions to the CH4 budget were reported from permafrost-underlain tundra in Alaska (Sturtevant et al. 2012; Zona et al. 2016). The short observation history in Adventdalen and gaps in the data, however, prevent a detailed analysis of this peak, leaving this task for future studies. Flux component A was either small or irregular compared to Zackenberg, which could be related to climatic differences during wintertime. At Zackenberg, despite the proximity to the sea (which is ice-covered for a large part of the year), the climate is stable and continental. Wintertime air temperature typically varies between −10 and −30 °C. In combination with the relatively thick snow cover of up to 1.3 m at the site (Pedersen et al. 2016), the harsh conditions lead to a constant soil temperature, which is low enough to suppress microbial decomposition processes until the soil starts to thaw (around the day of snowmelt). Adventdalen, on the other hand, has a maritime climate with changeable weather in wintertime. Air temperature can rise above 0 °C in episodic warm spells in the autumn, winter, and spring. Together with the relatively thin snow cover of about 20–30 cm, which can melt and refreeze repeatedly, this leads to a strongly varying soil temperature and episodic warming of the top of the permafrost. CH4 attributed to type A decomposition, therefore, may have escaped to the atmosphere before complete snowmelt in May, and was not captured by our measurements. Thus, flux component B is predominant at this site during the growing season. Furthermore, due to the polygonal ground pattern in Adventdalen and the associated differences in soil wetness, the flux magnitude varies strongly on small spatial scales. The overall interannual temperature variations as quantified by the total growing degree days are relatively small (cf. Fig. 5b) and explain little of the interannual variations of CH4 emissions.
Arctic winter precipitation is both observed and projected to change with climate warming, affecting snow cover differently depending on the season and region within the Arctic (Callaghan et al. 2011b; Derksen and Brown 2012). Arctic coastal regions (such as our sites) are likely to experience strong decreases of snow cover duration due to an earlier snowmelt in spring (Callaghan et al. 2011b), which would prolong the growing season. At each of our three sites, there was no indication that an earlier snowmelt would increase the total seasonal amount of emitted CH4 (cf. Fig. 5a). This finding is in line with Oberbauer et al. (1998), who observed no statistically significant difference in total CH4 emissions in a snow removal experiment in Alaskan tundra. Variations of the wintertime snow thickness, on the other hand, were found to increase CH4 emission, largely as a response to soil warming (Blanc-Betes et al. 2016). So it could be argued that the shorter growing season could be compensated by typically higher soil temperature (higher CH4 fluxes) in years with a thick, long-lasting snowpack (Stiegler et al. 2016). Reciprocally, an earlier snowmelt can in part be due to less wintertime precipitation, which in turn leads to a lower water table position upon melt in summertime and therefore lower CH4 fluxes. Note, however, that these interannual differences can in the long term be overruled by climate warming and potential permafrost thawing, which is expected to increase both CH4 and CO2 emissions (Schädel et al. 2016).
The CH4 emission patterns differed strongly between the three measurement sites. The Zackenberg site featured two clearly distinct flux components during the growing season, which responded differently to the timing of snowmelt, as expected from the bi-component hypothesis. Zackenberg and Adventdalen showed a third component during the autumnal freeze-in period, which is presumably caused by physical mechanisms in permafrost regions (Pirk et al. 2015). The absence of such large CH4 autumn bursts at Kobbefjord, where seasonal ground freezing without permafrost occurs, remains to be investigated in future studies with measurements covering this period. To further investigate the origin of the different flux components, future studies could aim to measure the isotopic signature of the CH4 source to resolve potential differences between components A, B, and C. From the present study, we expect more distinct source variations at Zackenberg than at Kobbefjord and Adventdalen, where growing season emissions appear dominated by one single component (B). Another approach could involve laboratory studies with soil samples from the different sites, which could be subjected to freeze–thaw cycles to study type A fluxes. With a better understanding of the different components, the modeling of CH4 fluxes using the specifics of the underlying processes can be improved. Our statistical analysis of CH4 emission from arctic wetlands can be used to predict the temporal flux patterns based on a minimal amount of information, namely the timing of snowmelt. Across the sites and years, the seasonality of the flux patterns was related to the timing of snowmelt, which did, however, not significantly affect the total seasonal budget.
Data were provided by the Greenland Ecosystem Monitoring Program supported by the Danish Energy Agency. The research leading to these results has received funding from the European Community’s Seventh Framework Program (FP7) under Grants 238366, 262693, and 282700, and the Nordic Centers of Excellence DEFROST and eSTICC (eScience Tool for Investigating Climate Change in northern high latitudes) funded by Nordforsk (Grant 57001).
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