ALBERT

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: Although methane is a widely studied greenhouse gas, uncertainties remain with respect to the factors controlling its distribution and diffusive flux into the atmosphere, especially in highly dynamic coastal waters. In the southern North Sea, the Elbe and Weser rivers are two major tributaries contributing to the overall methane budget of the southern German Bight. In June 2019, we continuously measured methane and basic hydrographic parameters at a high temporal and spatial resolution (one measurement per minute every 200–300 m) on a transect between Cuxhaven and Helgoland. These measurements revealed that the overall driver of the coastal methane distribution is the dilution of riverine methane-rich water with methane-poor marine water. For both the Elbe and Weser, we determined an input concentration of 40–50 nmol/L compared to only 5 nmol/L in the marine area. Accordingly, we observed a comparatively steady dilution pattern of methane concentration toward the marine realm. Moreover, small-scale anomalous patterns with unexpectedly higher dissolved methane concentrations were discovered at certain sites and times. These patterns were associated with the highly significant correlations of methane with oxygen or turbidity. However, these local anomalies were not consistent over time (days, months). The calculated diffusive methane flux from the water into the atmosphere revealed local values approximately 3.5 times higher than background values (median of 36 and 128 μmol m–2 d–1). We evaluate that this occurred because of a combination of increasing wind speed and increasing methane concentration at those times and locations. Hence, our results demonstrate that improved temporal and spatial resolution of methane measurements can provide a more accurate estimation and, consequently, a more functional understanding of the temporal and spatial dynamics of the coastal methane flux.

Description: MOSES (Modular Observation Solutions for Earth Systems) is a novel observation system that is specifically designed to unravel the impact of distinct, dynamic events on the long-term development of environmental systems. Hydro-meteorological extremes such as the recent European droughts or the floods of 2013 caused severe and lasting environmental damage. Modelling studies suggest that abrupt permafrost thaw events accelerate Arctic greenhouse gas emissions. Short-lived ocean eddies seem to comprise a significant share of the marine carbon uptake or release. Although there is increasing evidence that such dynamic events bear the potential for major environmental impacts, our knowledge on the processes they trigger is still very limited. MOSES aims at capturing such events, from their formation to their end, with high spatial and temporal resolution. As such, the observation system extends and complements existing national and international observation networks, which are mostly designed for long-term monitoring.Several German Helmholtz Association centers have developed this research facility as a mobile and modular “system of systems” to record energy, water, greenhouse gas and nutrient cycles on the land surface, in coastal regions, in the ocean, in polar regions, and in the atmosphere – but especially the interactions between the Earth compartments. During the implementation period (2017-2021), the measuring systems were put into operation and test campaigns were performed to establish event-driven campaign routines. With MOSES’ regular operation starting in 2022, the observation system will then be ready for cross-compartment and cross-discipline research on the environmental impacts of dynamic events.

Description: Rivers are suspected to be a main suppliers of greenhouse gases (methane and carbon dioxide) to coastal seas, while the role of the interjacent tidal flats is still ambiguous. In this study we investigated the role of the Elbe and Weser estuaries as source of methane to the North Sea. We used high spatially resolved methane measurements from an underway degassing system and subsequent analysis with cavity ring down spectroscopy. Thus, a high-resolution representation of the methane distribution in surface waters as well as of hydrographic parameters was obtained for several cruises with two ships in 2019. For most areas, riverine methane was simply diluted by seawater, overlain by a strong tidal signal. However, on several occasions unexpectedly high methane concentrations were observed. Further detailed analysis will elucidate the role of riverine versus tidal impact on coastal North Sea methane fluxes.

Description: Understanding river-sea-systems requires a thorough understanding of processes that span different Earth system compartments. To overcome issues related to the interaction of different scientific disciplines and compartments, such as different measurement and calibration standards, quality control approaches and data formats for specific environmental parameters, joint measurement campaigns have been initiated within the Helmholtz Association’s MOSES (Modular Observation Solutions for Earth Systems) project. Following multiple senor comparison and intercalibration campaigns in 2019, MOSES’ Hydrological Extremes event chain working group initiated joint field campaigns in summer 2020 covering the Elbe river from the Czech-German border to the tidal Elbe and further on into the estuary and the German Bight. The fundamental objective was to establish scientifically sound and resilient multi-ship applicable sampling procedures and to create reference data for the main environmental parameters for future investigation of extreme events such as flooding and drought and their overall impact on the catchment region and the adjacent estuarine area of a large European fresh water / marine system. The campaign involved four research vessels, four research centers and spanned nearly two months. Measurements included standard hydrological and oceanographic parameters, as well as quantities relevant to the nutrient and carbonate system. Furthermore, selected water quality indicators and atmospheric measurements were performed. In the fresh water section of the Elbe river measurements were taken while drifting with the water mass. In the tidal section of the river sampling was done against the ebb current while in the North Sea a grid covering a large part of the German exclusive economic zone (EEZ) was sampled. We detected a longitudinal increase of phytoplankton biomass along the 585 km freshwater part of the river towards the tidal system. In contrast, concentrations of dissolved nitrate and phosphate decreased to low values due the uptake by planktonic algae. The concentration of dissolved CO2 decreased caused by increasing photosynthesis while the concentration of methane increased along the river stretch, particularly in the most downstream part when sedimentation of phytoplankton increased the organic load of sediments. The tidal part of the transect showed a strong influence of Hamburg harbor on almost all quantities, while downstream towards the estuary, the effects of the tidal cycle dominated variabilities. In the marine area, elevated chlorophyll concentrations were mainly found near the west coast of Schleswig-Holstein, probably mostly influenced by the Eider river outflow or the adjacent tidal flats. While most of the measured parameters showed an expected behavior relative to their individual compartments, the transfer of quantities between the compartments revealed rather complex and sometimes difficult to understand behaviors and patterns, especially when considering a functional quantitative analysis. The first results of this trans-compartment campaign showed that a quantitative understanding of the fate and dynamics of water constituents across compartments from the spring to the sea needs enhanced scientific collaboration and awareness to finally come to a better integrated understanding of physical, biogeochemical and biological processes from the local to the global scale.

Description: Surface waters are known to be significant sources of greenhouse gases (CH4 and CO2), but our understanding of large scale patterns is still incomplete. The greenhouse gases in rivers originate both from in-stream processes and interactions with the catchment. For coastal seas, rivers are suspected to be one of the main source of greenhouse gases, while the role of the interjacent tidal flats is still ambiguous. Especially the reaction of the entire system on terrestrial hydrological extremes such as low flow situations are still under consideration. The functional understanding of such events and their impacts on the water chemistry along its transition pathway in the terrestrial and limnic compartment as well as in the coastal marine environment is crucially needed for the evaluation of its relevance in the Earth system. As part of a MOSES campaign (Modular Observation Solutions for Earth Systems) spanning disciplines as well as earth system compartments we investigated the aquatic as well as the atmospheric compartemt in and above the Elbe River from inland waters through the tidal section of the river and the estuary to the North Sea with the goal to explore spatial heterogeneity of CO2 and CH4 concentrations in the water and in ambient air above the water during a low water period in summer 2020. Overall, dissolved CH4 concentrations ranged over three orders of magnitude. Along the freshwater part of the transect, dissolved CH4 increased and weirs and harbors appeared to be hot spots of elevated CH4 concentrations both for the dissolved and atmospheric phase. We observed a longitudinal gradient of CO2 in the river which was closely linked to primary production. In the estuary and the marine part, dissolved CH4 concentrations of the transect were determined by the variability of temperature and salinity. Correlations with other water parameters revealed the complex regulation of dissolved CH4 concentrations along the freshwater-seawater continuum. For atmospheric CH4 above the North Sea, wind direction and wind speed proved to be crucial. Besides the typical diurnal fluctuations of atmospheric CO2 and CH4, an observed link between dissolved and atmospheric concentrations has to be further clarified.

Description: We investigated the impact of kelp deposition on the geochemistry and microbial community composition of beach sands on the island of Helgoland (North Sea). The composition of the microbial community at a beach with regular kelp deposition appeared shaped by this regular input of organic material, as indicated by significantly higher proportions of aerobic degraders, fermenters, and sulfur cycling microorganisms. Rapid degradation of deposited kelp by this community leads to high levels of dissolved organic and inorganic carbon and nutrients, a lower pH and anoxia. Aerobic respiration, fermentation, Fe- and SO42- reduction and methanogenesis were strongly enhanced, with SO42- reduction being the main process in kelp degradation. SO42- reduction rates increased 20 to 25-fold upon addition of kelp. The main route of electrons from kelp to SO42- was not via CO and H2, as expected, but via organic fermentation products. O2 supply by the tides was not sufficient and reduced intermediates escaped from the sediment with tidal water retraction. The resulting extremely high levels of free sulfide (〉10 mmol L-1) lead to abundant filamentous growth of sulfur-oxidizing bacteria largely composed of a rare O2-adapted Sulfurovum lacking the expected denitrification genes. Our results show that regular kelp deposition strongly enhances the thermodynamic disequilibrium in the beach sand habitat, leading to a dramatic enhancement of the sulfur cycle.