ALBERT

Description: The ocean and inland waters are two separate regimes, with concentrations in greenhouse gases differing on orders of magnitude between them. Together, they create the land–ocean aquatic continuum (LOAC), which comprises itself largely of areas with little to no data with regards to understanding the global carbon system. Reasons for this include remote and inaccessible sample locations, often tedious methods that require collection of water samples and subsequent analysis in the lab, and the complex interplay of biological, physical and chemical processes. This has led to large inconsistencies, increasing errors and has inevitably lead to potentially false upscaling. A set-up of multiple pre-existing oceanographic sensors allowing for highly detailed and accurate measurements was successfully deployed in oceanic to remote inland regions over extreme concentration ranges. The set-up consists of four sensors simultaneously measuring pCO2, pCH4 (both flow-through, membrane-based non-dispersive infrared (NDIR) or tunable diode laser absorption spectroscopy (TDLAS) sensors), O2 and a thermosalinograph at high resolution from the same water source. The flexibility of the system allowed for deployment from freshwater to open ocean conditions on varying vessel sizes, where we managed to capture day–night cycles, repeat transects and also delineate small-scale variability. Our work demonstrates the need for increased spatiotemporal monitoring and shows a way of homogenizing methods and data streams in the ocean and limnic realms.

Description: Methane (CH4) is one of the substantial greenhouse gases in our atmosphere and its concentration has increased by ~ 4 % over the last decade. Although sources driving these increases are not well constrained, one potential contribution comes from wetlands, which are usually intertwined with rivers, channels and lakes, creating a considerable need to acquire higher resolution data to facilitate 5 modelling and predictions. Here we took a fully contained sensor set-up to obtain measurements of CO2, CH4, O2 and auxiliary parameters, installed on a houseboat for accessibility, to assess and analyse surface water concentrations within the Danube Delta, Romania. Over 3 seasons, we transected a ~ 400 km route with concentration mapping and additional stations for monitoring diel cycles. Overall, the delta was a source for CH4 throughout all seasons, with concentrations ranging between 0.113–15.6 μmol L−1. The dataset was split into three different subsystems; lakes, rivers and channels, with channels 10 showing the highest variability. We found large to extreme diel cycles in both the lakes and channels, with concentrations varying by an order of magnitude between these two systems. The observed strong diel cycle within the lake suggests daily vertical stratification allowing for macrophytes to create a temporal oxycline due to lack of light and movement between the stems as previously suggested. While throughout the day, there was a consistent overall surface concentration of CH4 at around 0.4 μmol L−1, there was a clear linear trend with an O2:CH4 molar ratio of −50:1 during the phase of nocturnal convection 15 with the two water stratified bodies mixing during the night. Daily spot sampling techniques and neglecting such diel cycles reducing the estimated average methane concentrations by 25 % and increase by 3.3 % for channels and lakes, respectively. On an individual lake basis, spot sampling can potentially incur an uncertainty range of a factor of 4.5. Analyses also included a ‘hot spot’, with a 10-fold stronger methane increase (4–15.6 μmol L−1) overnight compared to the lake, with an almost immediate and extreme decrease in CH4 following sunrise. Calculated diffusive CH4 fluxes for the overall delta yielded an 20 average of 49 ± 61 μmol m−2 h−1 corresponding to an extrapolated annual flux of 0.43 ± 0.53 μmol m−2 yr−1. Our data illustrate the importance of collecting information on diel cycles in different habitats to improve the emission estimates from wetland systems.

Description: Mesoscale eddies are abundant in the eastern tropical North Atlantic and act as oases for phytoplankton growth due to local enrichment of nutrients in otherwise oligotrophic waters. It is not clear whether these eddies can efficiently transfer organic carbon and other flux components to depth and if they are important for the marine carbon budget. Due to their transient and regionally restricted nature, measurements of eddies' contribution to bathypelagic particle flux are difficult to obtain. Rare observations of export flux associated with low-oxygen eddies have suggested efficient export from the surface to the deep ocean, indicating that organic carbon flux attenuation might be low. Here we report on particle flux dynamics north of the Cabo Verde islands at the oligotrophic Cape Verde Ocean Observatory (CVOO; approx. 17∘35′ N, 24∘15′ W). The CVOO site is located in the preferred pathways of highly productive eddies that ultimately originate from the Mauritanian upwelling region. Between 2009 and 2016, we collected biogenic and lithogenic particle fluxes with sediment traps moored at ca. 1 and 3 km water depths at the CVOO site. From concurrent hydrography and oxygen observations, we confirm earlier findings that highly productive eddies are characterized by colder and less saline waters and a low-oxygen signal as well. Overall, we observed quite consistent seasonal flux patterns during the passage of highly productive eddies in the winters of 2010, 2012 and 2016. We found flux increases at 3 km depth during October–November when the eddies approached CVOO and distinct flux peaks during February–March, clearly exceeding low oligotrophic background fluxes during winter 2011 and showing an enhanced particle flux seasonality. During spring, we observed a stepwise flux decrease leading to summer flux minima. The flux pattern of biogenic silicate (BSi) showed a stronger seasonality compared to organic carbon. Additionally, the deep fluxes of total mass showed an unusually higher seasonality compared to the 1 km traps. We assume that BSi and organic carbon/lithogenic material had different sources within the eddies. BSi-rich particles may originate at the eddy boundaries where large diatom aggregates are formed due to strong shear and turbulence, resulting in gravitational settling and, additionally, in an active local downward transport. Organic carbon associated with lithogenic material is assumed to originate from the interior of eddies or from mixed sources, both constituting smaller, dust-ballasted particles. Our findings suggest that the regularly passing highly productive eddies at CVOO repeatedly release characteristic flux signals to the bathypelagic zone during winter–spring seasons that are far above the oligotrophic background fluxes and sequester higher organic carbon than during oligotrophic settings. However, the reasons for a lower carbon flux attenuation below eddies remain elusive.

Description: Multibeam bathymetry raw data was recorded in the Atlantic during cruise M160 that took place between2019-11-23 and 2019-12-20. The data was collected using the ship's own Kongsberg EM 122. This data is part of the DAM (German Marine Research Alliance) underway research data project.