| 1. |
- Douglas, Peter M. J., et al.
(författare)
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Clumped Isotopes Link Older Carbon Substrates With Slower Rates of Methanogenesis in Northern Lakes
- 2020
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Ingår i: Geophysical Research Letters. - 0094-8276 .- 1944-8007. ; 47:6
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Tidskriftsartikel (refereegranskat)abstract
- The release of long-stored carbon from thawed permafrost could fuel increased methanogenesis in northern lakes, but it remains unclear whether old carbon substrates released from permafrost are metabolized as rapidly by methanogenic microbial communities as recently produced organic carbon. Here, we apply methane (CH4) clumped isotope (Delta(18)) and C-14 measurements to test whether rates of methanogenesis are related to carbon substrate age. Results from culture experiments indicate that Delta(18) values are negatively correlated with CH4 production rate. Measurements of ebullition samples from thermokarst lakes in Alaska and glacial lakes in Sweden indicate strong negative correlations between CH4 Delta(18) and the fraction modern carbon. These correlations imply that CH4 derived from older carbon substrates is produced relatively slowly. Relative rates of methanogenesis, as inferred from Delta(18) values, are not positively correlated with CH4 flux estimates, highlighting the likely importance of environmental variables other than CH4 production rates in controlling ebullition fluxes. Plain Language Summary There is concern that carbon from thawed permafrost will be emitted to the atmosphere as methane (CH4). It is currently uncertain whether old organic carbon from thawed permafrost can be converted to CH4 as rapidly as organic carbon recently fixed by primary producers. We address this question by combining radiocarbon and clumped isotope measurements of CH4 from lakes in permafrost landscapes. Radiocarbon (C-14) measurements indicate the age of CH4 carbon sources. We present data from culture experiments that support the hypothesis that clumped isotope values are dependent on microbial CH4 production rate. In lake bubble samples, we observe a strong correlation between these two measurements, which implies that CH4 formed from older carbon is produced relatively slowly. We also find that higher rates of CH4 production, as inferred from clumped isotopes, are not linked to higher rates of CH4 emissions, implying that variables other than CH4 production rate strongly influence emission rates.
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| 2. |
- Jansen, Joachim, et al.
(författare)
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Drivers of diffusive lake CH4 emissions on daily to multi-year time scales
- 2020
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Ingår i: Biogeosciences. - : Copernicus GmbH. - 1726-4170 .- 1726-4189. ; 17:7, s. 1911-1932
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Tidskriftsartikel (refereegranskat)abstract
- Lakes and reservoirs are important emitters of climate forcing trace gases. Various environmental drivers of the flux, such as temperature and wind speed, have been identified, but their relative importance remains poorly understood. Here we use an extensive field dataset to disentangle physical and biogeochemical controls on the turbulence-driven diffusive flux of methane (CH4) on daily to multi-year timescales. We compare 8 years of floating chamber fluxes from three small, shallow subarctic lakes (2010–2017, n = 1306) with fluxes computed using 9 years of surface water concentration measurements (2009–2017, n = 606) and a small-eddy surface renewal model informed by in situ meteorological observations. Chamber fluxes averaged 6.9 ± 0.3 mg m−2 d−1 and gas transfer velocities (k600) from the chamber-calibrated surface renewal model averaged 4.0 ± 0.1 cm h−1. We find robust (R2 ≥ 0.93, p < 0.01) Arrhenius-type temperature functions of the CH4 flux (Ea' = 0.90 ± 0.14 eV) and of the surface CH4 concentration (Ea' = 0.88 ± 0.09 eV). Chamber derived gas transfer velocities tracked the power-law wind speed relation of the model (k ∝ u3/4). While the flux increased with wind speed, during storm events (U10 ≥ 6.5 m s−1) emissions were reduced by rapid water column degassing. Spectral analysis revealed that on timescales shorter than a month emissions were driven by wind shear, but on longer timescales variations in water temperature governed the flux, suggesting emissions were strongly coupled to production. Our findings suggest that accurate short- and long term projections of lake CH4 emissions can be based on distinct weather- and climate controlled drivers of the flux.
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| 3. |
- Jansen, Joachim, et al.
(författare)
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Temperature Proxies as a Solution to Biased Sampling of Lake Methane Emissions
- 2020
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Ingår i: Geophysical Research Letters. - 0094-8276 .- 1944-8007. ; 47:14
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Tidskriftsartikel (refereegranskat)abstract
- Lake emissions of the climate forcing trace gas methane (CH4) are spatiotemporally variable, but biases in flux measurements arising from undersampling are poorly quantified. We use a multiyear data set (2009-2017) of ice-free CH(4)emissions from three subarctic lakes obtained with bubble traps (n = 14,677), floating chambers (n = 1,306), and surface concentrations plus a gas transfer model (n = 535) to quantify these biases and evaluate corrections. Sampling primarily in warmer summer months, as is common, overestimates the ice-free season flux by a factor 1.4-1.8. Temperature proxies based on Arrhenius functions that closely fit measured fluxes (R-2 >= 0.93) enable gap filling the colder months of the ice-free season and reduce sampling bias. Ebullition (activation energy 1.36 eV) expressed greater temperature sensitivity than diffusion (1.00 eV). Resolving seasonal and interannual variability in fluxes with proxies requires similar to 135 sampling days for ebullition, and 22 and 14 days for diffusion via models and chambers, respectively.
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| 4. |
- Nguyen, Thanh Duc, et al.
(författare)
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Technical note: Greenhouse gas flux studies: an automated online system for gas emission measurements in aquatic environments
- 2020
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Ingår i: Hydrology and Earth System Sciences. - : COPERNICUS GESELLSCHAFT MBH. - 1027-5606 .- 1607-7938. ; 24:7, s. 3417-3430
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Tidskriftsartikel (refereegranskat)abstract
- Aquatic ecosystems are major sources of greenhouse gases (GHGs). Robust measurements of natural GHG emissions are vital for evaluating regional to global carbon budgets and for assessing climate feedbacks of natural emissions to improve climate models. Diffusive and ebullitive (bubble) transport are two major pathways of gas release from surface waters. To capture the high temporal variability of these fluxes in a well-defined footprint, we designed and built an inexpensive device that includes an easily mobile diffusive flux chamber and a bubble counter all in one. In addition to automatically collecting gas samples for subsequent various analyses in the laboratory, this device also utilized a low-cost carbon dioxide (CO2) sensor (SenseAir, Sweden) and methane (CH4) sensor (Figaro, Japan) to measure GHG fluxes. Each of the devices was equipped with an XBee module to enable local radio communication (DigiMesh network) for time synchronization and data readout at a server controller station on the lakeshore. The software of this server controller was operated on a lowcost computer (Raspberry Pi), which has a 3G connection for remote control and monitor functions from anywhere in the world. This study shows the potential of a low-cost automatic sensor network system for studying GHG fluxes on lakes in remote locations.
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| 5. |
- Nguyen, Thanh, et al.
(författare)
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Technical note : Greenhouse gas flux studies
- 2020
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Ingår i: Hydrology and Earth System Sciences. - : Copernicus GmbH. - 1027-5606 .- 1607-7938. ; 24:7, s. 3417-3430
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Tidskriftsartikel (refereegranskat)abstract
- Aquatic ecosystems are major sources of greenhouse gases (GHGs). Robust measurements of natural GHG emissions are vital for evaluating regional to global carbon budgets and for assessing climate feedbacks of natural emissions to improve climate models. Diffusive and ebullitive (bubble) transport are two major pathways of gas release from surface waters. To capture the high temporal variability of these fluxes in a well-defined footprint, we designed and built an inexpensive device that includes an easily mobile diffusive flux chamber and a bubble counter all in one. In addition to automatically collecting gas samples for subsequent various analyses in the laboratory, this device also utilized a low-cost carbon dioxide (CO2) sensor (SenseAir, Sweden) and methane (CH4) sensor (Figaro, Japan) to measure GHG fluxes. Each of the devices was equipped with an XBee module to enable local radio communication (DigiMesh network) for time synchronization and data readout at a server controller station on the lakeshore. The software of this server controller was operated on a lowcost computer (Raspberry Pi), which has a 3G connection for remote control and monitor functions from anywhere in the world. This study shows the potential of a low-cost automatic sensor network system for studying GHG fluxes on lakes in remote locations.
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| 6. |
- Wik, Martin, et al.
(författare)
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Stable Methane Isotopologues From Northern Lakes Suggest That Ebullition Is Dominated by Sub-Lake Scale Processes
- 2020
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Ingår i: Journal of Geophysical Research - Biogeosciences. - 2169-8953 .- 2169-8961. ; 125:10
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Tidskriftsartikel (refereegranskat)abstract
- Stable isotopes have emerged as popular study targets when investigating emission of methane (CH4) from lakes. Yet little is known on how isotopic patterns conform to variations in emission magnitudes—a highly relevant question. Here, we present a large multiyear data set on stable isotopes of CH4 ebullition (bubbling) from three small adjacent subarctic lakes. The δ13C‐CH4 and δD‐CH4 range from −78.4‰ to −53.1‰ and from −369.8‰ to −218.8‰, respectively, and vary greatly among the lakes. The signatures suggest dominant hydrogenotrophic methanogenesis, particularly in the deep zones, but there are also signals of seemingly acetoclastic production in some high fluxing shallow areas, possibly fueled by in situ vegetation, but in‐sediment anaerobic CH4 oxidation cannot be ruled out as an alternative cause. The observed patterns, however, are not consistent across the lakes. Neither do they correspond to the spatiotemporal variations in the measured bubble CH4 fluxes. Patterns of acetoclastic and hydrogenotrophic production plus oxidation demonstrate that gains and losses of sediment CH4 are dominated by sub‐lake scale processes. The δD‐CH4 in the bubbles was significantly different depending on measurement month, likely due to evaporation effects. On a larger scale, our isotopic data, combined with those from other lakes, show a significant difference in bubble δD‐CH4 between postglacial and thermokarst lakes, an important result for emission inventories. Although this characteristic theoretically assists in source partitioning studies, most hypothetical future shifts in δD‐CH4 due to high‐latitude lake area or production pathway are too small to lead to atmospheric changes detectable with current technology.
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