• European Marine Science
• SI close
• Biogeosciences close

Abstract. The eruption of the Eyjafjallajökull volcano starting on 14 April 2010 resulted in the spreading of volcanic ash over most parts of Europe. In Slovenia, the presence of volcanic ash was monitored using ground-based in-situ measurements, lidar-based remote sensing and airborne in-situ measurements. Volcanic origin of the detected aerosols was confirmed by subsequent spectral and chemical analysis of the collected samples. The initial arrival of volcanic ash to Slovenia was first detected through the analysis of precipitation, which occurred on 17 April 2010 at 01:00 UTC and confirmed by satellite-based remote sensing. At this time, the presence of low clouds and occasional precipitation prevented ash monitoring using lidar-based remote sensing. The second arrival of volcanic ash on 20 April 2010 was detected by both lidar-based remote sensing and airborne in-situ measurements, revealing two or more elevated atmospheric aerosol layers. The ash was not seen in satellite images due to lower concentrations. The identification of aerosol samples from ground-based and airborne in-situ measurements based on energy-dispersive X-ray spectroscopy confirmed that a fraction of particles were volcanic ash from the Eyjafjallajökull eruption. To explain the history of the air masses bringing volcanic ash to Slovenia, we analyzed airflow trajectories using ECMWF and HYSPLIT models.

Abstract. Hypoxia and anoxia have become a key threat to shallow coastal seas. Much is known about their impact on macrofauna, less on meiofauna. In an attempt to shed more light on the latter group, in particular from a process-oriented view, we experimentally induced short-term anoxia (1 week) in the Northern Adriatic Sea, Mediterranean, and examined the two most abundant meiofauna taxa – harpacticoid copepods and nematodes. Both taxa also represent different ends of the tolerance spectrum, with copepods being the most sensitive and nematodes among the most tolerant. We compared two methods: CellTracker Green (CTG) – new labelling approach for meiofauna – with the traditional Rose Bengal (RB) staining method. CTG binds to active enzymes and therefore colours live organisms only. The two methods show considerable differences in the number of living and dead individuals of both meiofauna taxa. Generally, RB will stain dead but not yet decomposed copepods and nematodes equally as live ones. Specifically, RB significantly overestimated the number of living copepods in all sediment layers in anoxic samples, but not in any normoxic samples. In contrast, for nematodes, the methods did not show such a clear difference between anoxia and normoxia. Surprisingly, RB overestimated the number of living nematodes in the top sediment layer of normoxic samples, which implies an overestimation of the overall live nematofauna. For monitoring and biodiversity studies, the RB method might be sufficient, but for more fine-scaled (days, hours, tipping points) studies, especially on hypoxia and anoxia where it is necessary to resolve the course of events, CTG labelling is a better tool. Moreover, it clearly highlights the surviving species within the copepod or nematode community. As already accepted for foraminiferal research, we demonstrate that the CTG labelling is also valid for other meiofauna groups.

Abstract. Combined in situ and laboratory studies were conducted to document the effects of anoxia on the structure and functioning of meiobenthic communities, with special focus on harpacticoid copepods. In a first step, anoxia was created artificially by means of an underwater chamber at 24 m depth in the Northern Adriatic, Gulf of Trieste (Mediterranean). Nematodes were found as the most abundant taxon, followed by harpacticoid copepods. While nematode densities were not affected by treatment (anoxia/normoxia) or sediment depth, these factors had a significant impact on copepod abundances. Harpacticoid copepod family diversity, in contrast, was not affected by anoxic conditions, only by depth. Ectinosomatidae and Cletodidae were most abundant in both normoxic and anoxic samples. The functional response of harpacticoid copepods to anoxia was studied in a laboratory tracer experiment by adding 13C pre-labelled diatoms to sediment cores in order to test (1) if there is a difference in food uptake by copepods under normoxic and anoxic conditions and (2) whether initial (normoxia) feeding of harpacticoid copepods on diatoms results in a better survival of copepods in subsequent anoxic conditions. Independent of the addition of diatoms, there was a higher survival rate in normoxia than anoxia. The supply of additional food did not result in a higher survival rate of copepods in anoxia, which might be explained by the presence of a nutritionally better food source and/or a lack of starvation before adding the diatoms. However, there was a reduced grazing pressure by copepods on diatoms in anoxic conditions. This resulted in a modified fatty acid composition of the sediment. We concluded that anoxia not only impacts the survival of consumers (direct effect) but also of primary producers (indirect effect), with important implications for the recovery phase.

The temperature dependence of planktonic metabolism in the subtropical North Atlantic Ocean was assessed on the basis of measurements of gross primary production (GPP), community respiration (CR) and net community production (NCP), as well as experimental assessments of the response of CR to temperature manipulations. Metabolic rates were measured at 68 stations along three consecutive longitudinal transects completed during the Malaspina 2010 Expedition, in three different seasons. Temperature gradients were observed in depth and at basin and seasonal scale. The results showed seasonal variability in the metabolic rates, the highest rates being observed during the spring transect. The overall mean integrated GPP / CR ratio was 1.39 ± 0.27 decreasing from winter to summer, and the NCP for the subtropical North Atlantic Ocean during the cruises exhibits net autotrophy (NCP > 0) in about two-thirds (66%) of the total sampled communities. Also, we reported the activation energies describing the temperature dependence of planktonic community metabolism, which was generally higher for CR than for GPP in the subtropical North Atlantic Ocean, as the metabolic theory of ecology predicts. Furthermore, we made a comparison of activation energies describing the responses to in situ temperature in the field (EaCR Combining double low line 1.64 ± 0.36 eV) and those derived experimentally by temperature manipulations (EaCR Combining double low line 1.45 ± 0.6 eV), which showed great consistency. © 2014 Author(s). This is a contribution to the Malaspina Expedition 2010, funded by the INGENIO 2010 CONSOLIDER program (ref. CDS2008-00077) of the Spanish Ministry of Economy and Competitiveness. L. S. García-Corral was supported by a JAE Pre-doc fellowship from the Spanish National Research Council (CSIC) and the BBVA Foundation, Spain Peer Reviewed

International audience; Long-term experimental studies suggest that, under transient anoxic conditions, redox fronts within the sediment shift upwards, causing sequential rise and fall of ben-thic fluxes of reduced species (Mn(II), Fe(II) and S(-II)). In-faunal benthic organisms are associated with different re-dox fronts as micro-habitats and must be affected by such changes during natural hypoxia events. In order to document the geochemical evolution of the sediment during prolonged anoxia in the framework of an in situ experiment designed to mimic natural conditions, benthic chambers were deployed on the seafloor of the Northern Adriatic and sampled after 9, 30 and 315 days of incubation. Oxygen and sulfide were measured continuously in the early stages (9 days) of the experiment. High-resolution pore water profiles were sampled by DET probes and redox-sensitive species (S(VI), Mn(II) and Fe(II)) and alkalinity were measured. Starting oxygen saturation was about 80 % within the chamber. After 7 days, anoxia was established in the bottom waters within the chambers. Mn(II) and Fe(II) started diffusing towards the anoxic water column until they reached the surficial sediment. Being reoxidized there, Mn and Fe re-precipitated, giving a rusty coloration to the seafloor. Infau-nal species appeared at the sediment surface. After 20 days, all macro-organisms were dead. Decomposition of macro-organisms at the sediment-water interface generated S(-II) within the entire height of the chamber, leading to a downward flux of sulfides into the sediment, where they were quickly oxidized by metallic oxides or precipitated as FeS. S(-II) was below detection in the water column and pore waters at the end of the experiment. Our results suggest that S(-II) enrichment in the water column of coastal systems, which are episodically anoxic, is strongly controlled by the biomass of benthic macrofauna and its decay during anoxia, whereas its residence time in the water column is controlled by iron availability (as solid oxides or as dissolved reduced cations) within the sediment, even without water circulation.

Abstract. The impact of anoxia on meiobenthic copepod species was assessed by means of a field experiment. Four plexiglass chambers were deployed in situ in 24 m depth to simulate an anoxic event of 9 days, 1 month, 2 months and 10 months. From normoxic to anoxic conditions, we recorded a drop in copepod density and species richness. With increasing duration of anoxia the relative abundance of the individuals of the family Cletodidae increased, and they survived the 1 month and 2 month anoxia, the latter with few specimens. They were the true "winners" of the experimentally induced anoxia. Dominance did not increase throughout all deployments because; not one, but several species from this family were tolerant to anoxia. The overall rate of survival was the same for males and females, but no juvenile stages of copepods survived in anoxia. During a recovery phase of 7 days after a short-term anoxia of 9 days, harpacticoid copepod density did not increase significantly, and there was only a slight increase in species diversity. We concluded that there was no substantial colonisation from the surrounding sediment. The survivors, however, showed a high potential for recovery according to the number of gravid females, whose number increased significantly once the oxygen was available again. These finding imply that a substantial amount of energy is allocated to reproduction in the recovery phase.