Description: Rising stable nitrogen isotope ratios (δ15N) in dated sediment records of the German Bight/SE North Sea track river-induced coastal eutrophication over the last 2 centuries. Fully exploiting their potential for reconstructions of pristine conditions and quantitative analysis of historical changes in the nitrogen cycle from these sediment records requires knowledge on processes that alter the isotopic signal in non-living organic matter (OM) of sinking particles and sediments. In this study, we analyze the isotopic composition of particulate nitrogen (PN) in the water column during different seasons, in surface sediments, and in sediment cores to assess diagenetic influences on the isotopic composition of OM. Amino acid (AA) compositions of suspended matter, surface sediments, and dated cores at selected sites of the German Bight serve as indicators for quality and degradation state of PN. The δ15N of PN in suspended matter had seasonal variances caused by two main nitrate sources (oceanic and river) and different stages of nitrate availability during phytoplankton assimilation. Elevated δ15N values (〉 20‰) in suspended matter near river mouths and the coast coincide with a coastal water mass receiving nitrate with elevated isotope signal (δ15N 〉 10‰) derived from anthropogenic input. Particulate nitrogen at offshore sites fed by oceanic nitrate having a δ15N between 5 and 6‰ had low δ15N values (〈 2‰), indicative of an incipient phytoplankton bloom. Surface sediments along an offshore–onshore transect also reflect the gradient of low δ15N of nitrate in offshore sites to high values near river mouths, but the range of values is smaller than between the end members listed above and integrates the annual δ15N of detritus. Sediment cores from the coastal sector of the gradient show an increasing δ15N trend (increase of 2.5‰) over the last 150 years. This is not related to any change in AA composition and thus reflects eutrophication. The δ15N signals from before AD 1860 represent a good estimation of pre-industrial isotopic compositions with minimal diagenetic overprinting. Rising δ13C in step with rising δ15N in these cores is best explained by increasing productivity caused by eutrophication.

Description: The effect of the supply of chlorinated biphenyls by the river Oder into some adjacent areas of Baltic Sea was studied in nine sediment cores and in 10 suspended matter samples. Congener-specific analysis was carried out on 28 individual chlorobiphenyls (CBs). ∑CB concentrations in suspension ranged from 2.4 pg dm-3 in the southern Bornholm Basin to 986 pg dm-3 in the Achterwasser. ∑CB contents in surface sediment decreased with increasing distance from the river mouth. Highest contents were found in the Oderhaff (18 ng g-1 dw) decreasing to 2 ng g-1 dw in the Bornholm Basin. The ∑CB contents generally decreased more or less regularly with increasing depth. The compositions of the CB mixtures in surficial sediment and suspension samples were rather similar, suggesting a common source. Compositions of the CB mixtures in the sediment cores showed distinct differences. These may reflect variations in source strength over time. Mass balance considerations on the basis of the 28 CBs resulted in an estimation of a total storage of approximate 733±158 kg ∑CBs in the Oderhaff, Achterwasser, Greifswalder Bodden, Oder Rinne, Arkona Basin and Bornholm Basin in the past 65 years, covering the time period since CBs were first produced. Based on river data about 500 kg of ∑CBs were supplied during this time by river Oder, that may thus be the major source of these compounds for the southern Baltic Sea.

Description: The coastal ocean is strongly affected by ocean acidification because of its shallow water depths, low volume, and the closeness to terrestrial dynamics. Earlier observations of dissolved inorganic carbon (DIC) and total alkalinity (TA) in the southern part of the North Sea, a northwest European shelf sea, revealed lower acidification effects than expected. It has been assumed that anaerobic degradation and subsequent TA release in the adjacent back-barrier tidal areas (Wadden Sea) in summertime is responsible for this phenomenon. In this study the exchange rates of TA and DIC between the Wadden Sea tidal basins and the North Sea and the consequences for the carbonate system in the German Bight are estimated using a 3D ecosystem model. The aim of this study is to differentiate the various sources contributing to observed high summer TA in the southern North Sea. Measured TA and DIC in the Wadden Sea are considered as model boundary conditions. This procedure acknowledges the dynamic behaviour of the Wadden Sea as an area of effective production and decomposition of organic material. According to the modelling results, 39 Gmol TA yr−1 were exported from the Wadden Sea into the North Sea, which is less than a previous estimate but within a comparable range. The interannual variabilities in TA and DIC, mainly driven by hydrodynamic conditions, were examined for the years 2001–2009. Dynamics in the carbonate system are found to be related to specific weather conditions. The results suggest that the Wadden Sea is an important driver for the carbonate system in the southern North Sea. On average 41 % of TA inventory changes in the German Bight were caused by riverine input, 37 % by net transport from adjacent North Sea sectors, 16 % by Wadden Sea export, and 6 % were caused by internal net production of TA. The dominant role of river input for the TA inventory disappears when focusing on TA concentration changes due to the corresponding freshwater fluxes diluting the marine TA concentrations. The ratio of exported TA versus DIC reflects the dominant underlying biogeochemical processes in the Wadden Sea. Whereas aerobic degradation of organic matter played a key role in the North Frisian Wadden Sea during all seasons of the year, anaerobic degradation of organic matter dominated in the East Frisian Wadden Sea. Despite the scarcity of high-resolution field data, it is shown that anaerobic degradation in the Wadden Sea is one of the main contributors of elevated summer TA values in the southern North Sea.

Description: The westerlies and trade winds over the South Atlantic and Indian Ocean are important drivers of the regional oceanography around southern Africa, including features such as the Agulhas Current, the Agulhas leakage, and the Benguela upwelling. Agulhas leakage constitutes a fraction of warm and saline water transport from the Indian Ocean into the South Atlantic. The leakage is stronger during intensified westerlies. Here, we analyze the wind stress of different observational and modeled atmospheric data sets (covering the last 2 millennia, the recent decades, and the 21st century) with regard to the intensity and position of the southeasterly trades and the westerlies. The analysis reveals that variations of both wind systems go hand in hand and that a poleward shift of the westerlies and trades and an intensification of westerlies took place during the recent decades. Furthermore, upwelling in South Benguela is slightly intensified when trades are shifted poleward. Projections for strength and position of the westerlies in the 21st century depend on assumed CO2 emissions and on their effect relative to the ozone forcing. In the strongest emission scenario (RCP8.5) the simulations show a further southward displacement, whereas in the weakest emission scenario (RCP2.6) a northward shift is modeled, possibly due to the effect of ozone recovery dominating the effect of anthropogenic greenhouse forcing. We conclude that the Agulhas leakage has intensified during the last decades and is projected to increase if greenhouse gas emissions are not reduced. This will have a small impact on Benguela upwelling strength and may also have consequences for water mass characteristics in the upwelling region. An increased contribution of Agulhas water to the upwelling water masses will import more preformed nutrients and oxygen into the upwelling region.

Description: Amino acids (AAs) mainly bound in proteins are major constituents of living biomass and non-living organic material in the oceanic particulate and dissolved organic matter pool. Uptake and cycling by heterotrophic organisms lead to characteristic changes in AA composition so that AA-based biogeochemical indicators are often used to elucidate processes of organic matter cycling and degradation. We analyzed particulate AA in a large sample set collected in various oceanic regions covering sinking and suspended particles in the water column, sediment samples, and dissolved AA from water column and pore water samples. The aim of this study was to test and improve the use of AA-derived biogeochemical indicators as proxies for organic matter sources and degradation and to better understand particle dynamics and interaction between the dissolved and particulate organic matter pools. A principal component analysis (PCA) of all data delineates diverging AA compositions of sinking and suspended particles with increasing water depth. A new sinking particle and sediment degradation indicator (SDI) allows a fine-tuned classification of sinking particles and sediments with respect to the intensity of degradation, which is associated with changes of stable isotopic ratios of nitrogen (δ15N). This new indicator is furthermore sensitive to sedimentary redox conditions and can be used to detect past anoxic early diagenesis. A second indicator emerges from the AA spectra of suspended particulate matter (SPM) in the epipelagic and that of the meso- and bathypelagic ocean and is a residence time indicator (RTI). The characteristic changes in AA patterns from shallow to deep SPM are recapitulated in the AA spectra of the dissolved organic matter (DOM) pool, so that deep SPM is more similar to DOM than to any of the other organic matter pools. This implies that there is equilibration between finely dispersed SPM and DOM in the deep sea, which may be driven by microbial activity combined with annealing and fragmentation of gels. As these processes strongly depend on physico-chemical conditions in the deep ocean, changes in quality and degradability of DOM may strongly affect the relatively large pool of suspended and dissolved AA in the ocean that amounts to 15 Pg amino acid carbon (AAC) and 89 ± 29 Pg AAC, respectively.