ALBERT

Description: The Lena River is one of the biggest Russian rivers draining into the Laptev Sea. Due to predicted increasing temperatures, the permafrost areas surrounding the Lena Delta will melt at increasing rates. With this melting, high amounts of methane will reach the waters of the Lena and the adjacent Laptev Sea. Methane oxidation by methanotrophic bacteria is the only biological way to reduce methane concentrations within the system. However, the polar estuary of the Lena River is a challenging environment for bacteria, with strong fluctuations in salinity and temperature. We determined the activity (tracer method) and the abundance (qPCR) of aerobic methanotrophic bacteria. We described the methanotrophic population with MISA; as well as the methane distribution (head space) and other abiotic parameters in the Lena Delta in September 2013. In riverine water (S 〈 5) we found a median methane concentration of 22 nM, in mixed water (5 〈 S 〈 20) the median methane concentration was 19 nM and in polar water (S 〉 20) a median 28 nM was observed. The Lena River was not the methane source for surface water, and bottom water methane concentrations were mainly influenced by the concentration in surface sediments. However, the methane oxidation rate in riverine and polar water was very similar (0.419 and 0.400 nM/d), but with a higher relative abundance of methanotrophs and a higher estimated diversity with respect to MISA OTUs in the rivine water as compared to polar water. The turnover times of methane ranged from 167 d in mixed water, 91 d in riverine water and only 36 d in polarwater. Also the environmental parameters influencing the methane oxidation rate and the methanotrophic population differed between the water masses. Thus we postulate a riverine methanotrophic population limited by sub-optimal temperatures and substrate concentrations and a polar methanotrophic population being well adapted to the cold and methane poor environment, but limited by the nitrogen content. The diffusive methane flux into the atmosphere ranged from 4–163 µmol m2 d−1 (median 24). For the total methane inventory of the investigated area, the diffusive methane flux was responsible for 8 % loss, compared to only 1 % of the methane consumed by the methanotrophic bacteria within the system.

Description: The Lena River is one of the largest Russian rivers draining into the Laptev Sea. The predicted increases in global temperatures are expected to cause the permafrost areas surrounding the Lena Delta to melt at increasing rates. This melting will result in high amounts of methane reaching the waters of the Lena and the adjacent Laptev Sea. The only biological sink that can lower methane concentrations within this system is methane oxidation by methanotrophic bacteria. However, the polar estuary of the Lena River, due to its strong fluctuations in salinity and temperature, is a challenging environment for bacteria. We determined the activity and abundance of aerobic methanotrophic bacteria by a tracer method and by the quantitative polymerase chain reaction. We described the methanotrophic population with a molecular fingerprinting method (monooxygenase intergenic spacer analysis), as well as the methane distribution (via a headspace method) and other abiotic parameters, in the Lena Delta in September 2013. The median methane concentrations were 22 nmol L−1 for riverine water (salinity (S)  

Description: Arctic regions and their water bodies are affected by a rapidly warming climate. Arctic lakes and small ponds are known to act as an important source of atmospheric methane. However, not much is known about other types of water bodies in permafrost regions, which include major rivers and coastal bays as a transition type between freshwater and marine environments. We monitored dissolved methane concentrations in three different water bodies (Lena River, Tiksi Bay, and Lake Golzovoye, Siberia, Russia) over a period of 2 years. Sampling was carried out under ice cover (April) and in open water (July–August). The methane oxidation (MOX) rate and the fractional turnover rate (k′) in water and melted ice samples from the late winter of 2017 was determined with the radiotracer method. In the Lena River winter methane concentrations were a quarter of the summer concentrations (8 nmol L−1 vs. 31 nmol L−1), and mean winter MOX rate was low (0.023 nmol L−1 d−1). In contrast, Tiksi Bay winter methane concentrations were 10 times higher than in summer (103 nmol L−1 vs. 13 nmol L−1). Winter MOX rates showed a median of 0.305 nmol L−1 d−1. In Lake Golzovoye, median methane concentrations in winter were 40 times higher than in summer (1957 nmol L−1 vs. 49 nmol L−1). However, MOX was much higher in the lake (2.95 nmol L−1 d−1) than in either the river or bay. The temperature had a strong influence on the MOX (Q10=2.72±0.69). In summer water temperatures ranged from 7–14 ∘C and in winter from −0.7 to 1.3 ∘C. In the ice cores a median methane concentration of 9 nM was observed, with no gradient between the ice surface and the bottom layer at the ice–water interface. MOX in the (melted) ice cores was mostly below the detection limit. Comparing methane concentrations in the ice with the underlaying water column revealed methane concentration in the water column 100–1000 times higher. The winter situation seemed to favor a methane accumulation under ice, especially in the lake with a stagnant water body. While on the other hand, in the Lena River with its flowing water, no methane accumulation under ice was observed. In a changing, warming Arctic, a shorter ice cover period is predicted. With respect to our study this would imply a shortened time for methane to accumulate below the ice and a shorter time for the less efficient winter MOX. Especially for lakes, an extended time of ice-free conditions could reduce the methane flux from the Arctic water bodies.

Description: The thermokarst lakes of permafrost regions play a major role in the global carbon cycle. These lakes are sources of methane to the atmosphere although the methane flux is restricted by an ice cover for most of the year. How methane concentrations and fluxes in these waters are affected by the presence of an ice cover is poorly understood. To relate water body morphology, ice formation and methane to each other, we studied the ice of three different water bodies in locations typical of the transition of permafrost from land to ocean in a continuous permafrost coastal region in Siberia. In total, 11 ice cores were analyzed as records of the freezing process and methane composition during the winter season. The three water bodies differed in terms of connectivity to the sea, which affected fall freezing. The first was a bay underlain by submarine permafrost (Tiksi Bay, BY), the second a shallow thermokarst lagoon cut off from the sea in winter (Polar Fox Lagoon, LG) and the third a land-locked freshwater thermokarst lake (Goltsovoye Lake, LK). Ice on all water bodies was mostly methane-supersaturated with respect to atmospheric equilibrium concentration, except for three cores from the isolated lake. In the isolated thermokarst lake, ebullition from actively thawing basin slopes resulted in the localized integration of methane into winter ice. Stable δ13CCH4 isotope signatures indicated that methane in the lagoon ice was oxidized to concentrations close to or below the calculated atmospheric equilibrium concentration. Increasing salinity during winter freezing led to a micro-environment on the lower ice surface where methane oxidation occurred and the lagoon ice functioned as a methane sink. In contrast, the ice of the coastal marine environment was slightly supersaturated with methane, consistent with the brackish water below. Our interdisciplinary process study shows how water body morphology affects ice formation which mitigates methane fluxes to the atmosphere.

Description: ABSTRACT: Salinity is an important environmental control of aerobic methane oxidation, which reduces the emission of the potent greenhouse gas methane into the atmosphere. The effect of salinity on methane oxidation is especially severe in river estuaries and adjacent coastal waters, which are important sources of methane emission and, at the same time, are usually characterized by pronounced salinity gradients. Using methane oxidation rates determined by a radiotracer technique as a measure of methanotrophic activity, we tested the effect of immediate and gradual salinity changes on pure cultures of methanotrophic bacteria, and natural freshwater (Elbe River) and natural marine (North Sea) methanotrophic populations. According to our results, Methylomonas sp. and Methylosinus trichosporium are resistant to an increase in salinity, whereas Methylovulum sp. and Methylobacter luteus are sensitive to such an increase. Natural methanotrophic populations from freshwater are more resistant to an increase in salinity than those from marine water are to a decrease in salinity. In contrast to an immediate change of salinity, gradual change (1.25 PSU d−1) can attenuate salinity stress. Experiments with the natural populations revealed different reactions to changes in salinity; thus, we assume that the initial composition of the methanotrophic population, i.e. the ratio of sensitive versus resistant strains, also governs the community response to salinity stress.Repeated experiments with the natural populations revealed different reactions to changes of salinity; thus we assume that the initial composition of the methanotrophic population, i.e. the ratio of sensitive and resistant strains, also governs the community response to salinity stress.

Description: Shelf sea areas are the primary oceanic source for methane release, the most abundant hydrocarbon in the atmosphere. As such, the southern North Sea’s methane concentration is mainly determined by river runoff and tidal marshes. Within such a highly variable temperate estuary, this study is the first to reveal detailed information on the in situ activity, abundance and community structure of methane oxidizing bacteria along a transect from the marine environment near Helgoland island to the riverine harbor of Hamburg, Germany. The in situ methane oxidation rate was determined with a radio tracer, and methane concentration with the head-space method. Abundance and diversity of the methanotrophic bacterial community in the water column was assessed with quantitative polymerase chain reaction for the particulate methane monooxygenase and monooxygenase intergenic spacer analysis. Median abundances ranged from 2.8 × 104 cells l−1 in the marine environment to 7.5 × 105 cells l−1 in the riverine environment. Except for salinity, no conclusive linear correlation between any environmental parameter and the abundance of methanotrophs could be determined. Relating activity with abundance of methanotrophs showed that about 70% of the population is inactive, especially in the coastal and marine environment. This study found distinct operational taxonomic unit (OTU) community compositions among the 3 environmental categories (river, coast, marine). Several identified OTUs have been reported previously and imply a wide geographic occurrence. Overall, we propose that salinity is the most important driver of differing communities in the riverine, coastal and marine environment.

Description: The thermokarst lakes of permafrost regions play a major role in the global carbon cycle. These lakes are sources of methane to the atmosphere although the methane flux is restricted by an ice cover for most of the year. How methane concentrations and fluxes in these waters are affected by the presence of an ice cover is poorly understood. To relate water body morphology, ice formation and methane to each other, we studied the ice of three different water bodies in locations typical of the transition of permafrost from land to ocean in a continuous permafrost coastal region in Siberia. In total, 11 ice cores were analyzed as records of the freezing process and methane composition during the winter season. The three water bodies differed in terms of connectivity to the sea, which affected fall freezing. The first was a bay underlain by submarine permafrost (Tiksi Bay, BY), the second a shallow thermokarst lagoon cut off from the sea in winter (Polar Fox Lagoon, LG) and the third a land-locked freshwater thermokarst lake (Goltsovoye Lake, LK). Ice on all water bodies was mostly methane-supersaturated with respect to atmospheric equilibrium concentration, except for three cores from the isolated lake. In the isolated thermokarst lake, ebullition from actively thawing basin slopes resulted in the localized integration of methane into winter ice. Stable δ13C-CH4 isotope signatures indicated that methane in the lagoon ice was oxidized to concentrations close to or below the calculated atmospheric equilibrium concentration. Increasing salinity during winter freezing led to a micro-environment on the lower ice surface where methane oxidation occurred and the lagoon ice functioned as a methane sink. In contrast, the ice of the coastal marine environment was slightly supersaturated with methane, consistent with the brackish water below. Our interdisciplinary process study shows how water body morphology affects ice formation which mitigates methane fluxes to the atmosphere.