On October 10 2011 an underwater eruption gave rise to a novel shallow submarine volcano south of the island of El Hierro, Canary Islands, Spain. During the eruption large quantities of mantle-derived gases, solutes and heat were released into the surrounding waters. In order to monitor the impact of the eruption on the marine ecosystem, periodic multidisciplinary cruises were carried out. Here, we present an initial report of the extreme physical-chemical perturbations caused by this event, comprising thermal changes, water acidification, deoxygenation and metal-enrichment, which resulted in significant alterations to the activity and composition of local plankton communities. Our findings highlight the potential role of this eruptive process as a natural ecosystem-scale experiment for the study of extreme effects of global change stressors on marine environments.

[1] Enhancement of primary and export production following dust deposition pulses is well established for High Nutrient Low Chlorophyll regions, but the effect of atmospheric dust on the biogeochemistry of oligotrophic gyre regions remains unclear.Here we report atmospheric dust concentrations measured on Gran Canaria, Canary Islands, concomitantly with upper water biogeochemistry at the oligotrophic time series station ESTOC (European Station for Time series in the Ocean, Canary Islands) during a 2-year period from winter 1997 to 1999. ESTOC is located in the eastern subtropical Atlantic gyre about 100 km north of Gran Canaria and 500 km west of the Sahara, and receives aeolian dust episodically mainly in winter and summer. We found a close correlation of the magnitude of atmospheric dust concentration in winter with the magnitude of downward particle flux at ESTOC, mainly due to a relative increase in lithogenic matter and carbonate sedimentation. Higher aerosol concentration was not accompanied by higher primary or export production, however, indicating that phytoplankton production remained unaffected by atmospheric nitrogen supply on a seasonal or yearly timescale. However, by estimating bioavailable iron input and the need of the phytoplankton population, we found that the highly episodic dust pulses might exert a feast and famine effect on the phytoplankton. Despite the high lithogenic matter input, carbonate, mainly stemming from coccolithophorids, exceeded in importance the role of lithogenic matter as ballasting agent of sinking organic matter.

.[1] There are very few sets of long-term measurements of aerosol concentrations over the North Atlantic Ocean, yet such data is invaluable in quantifying atmospheric dust inputs to this ocean region. We present an 8-year record of total suspended particles (TSP) collected at three stations on Gran Canaria Island, Spain (Taliarte at sea level, Tafira 269 m above sea level (a.s.l.) and Pico de la Gorra 1930 m a.s.l.). Using wet and dry deposition measurements, the mean dust flux was calculated at 42.3 mg m À2 d À1

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International audienceDissolved Fe, Mn and Al concentrations (dFe, dMn and dAl hereafter) in surface waters and the water column of the Northeast Atlantic and the European continental shelf are reported. Following an episode of enhanced Saharan dust inputs over the Northeast Atlantic Ocean prior and during the cruise in March 1998, surface concentrations were enhanced up to 4 nmol L− 1 dFe, 3 nmol L− 1 dMn and 40 nmol L− 1 dAl and returned to 0.6 nmol L− 1 dFe, 0.5 nmol L− 1 dMn and 10 nmol L− 1 dAl towards the end of the cruise three weeks later. A simple steady state model (MADCOW, [Measures, C.I., Brown, E.T., 1996. Estimating dust input to the Atlantic Ocean using surface water aluminium concentrations. In: Guerzoni. S. and Chester. R. (Eds.), The impact of desert dust across the Mediterranean, Kluwer Academic Publishers, The Netherlands, pp. 301-311.]) was used which relies on surface ocean dAl as a proxy for atmospheric deposition of mineral dust. We estimated dust input at 1.8 g m− 2 yr− 1 (range 1.0-2.9 g m− 2 yr− 1) and fluxes of dFe, dMn and dAl were inferred. Mixed layer steady state residence times for dissolved metals were estimated at 1.3 yr for dFe (range 0.3-2.9 yr) and 1.9 yr for dMn (range 1.0-3.8 yr). The dFe residence time may have been overestimated and it is shown that 0.2-0.4 yr is probably more realistic. Using vertical dFe versus Apparent Oxygen Utilization (AOU) relationships as well as a biogeochemical two end member mixing model, regenerative Fe:C ratios were estimated respectively to be 20 ± 6 and 22 ± 5 μmol Fe:mol C. Combining the atmospheric flux of dFe to the upper water column with the latter Fe:C ratio, a 'new iron' supported primary productivity of only 15% (range 7%-56%) was deduced. This would imply that 85% (range 44-93%) of primary productivity could be supported by regenerated dFe. The open ocean surface data suggest that the continental shelf is probably not a major source of dissolved metals to the surface of the adjacent open ocean. Continental shelf concentrations of dMn, dFe, and to a lesser extent dAl, were well correlated with salinity and express mixing of a fresher continental end member with Atlantic Ocean water flowing onto the shelf. This means probably that diffusive benthic fluxes did not play a major role at the time of the cruise

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A modification of the method for the determination of aluminium by adsorptive cathodic stripping voltammetry of its 1,2-dihydroxyanthraquinone-3-sulfonic acid (DASA) complex is described. Rapid determination is achieved by using staircase modulation and high potential scan speeds (20 V s-1). Square wave modulation was found inefficient above 2 V s-1 because the potential pulse is distorted by the ohmic drop. The staircase modulation is also distorted, but the determination is not disturbed and high faradaic currents are obtained. The method was not sensitive to the turbulence of the solution during the scan, as a short scan time is required (several ms) and very high currents (FA) are obtained from the reduction of the DASA-A1 complex. Interference from oxygen was also overcome as DASA-A1 to oxygen current ratios are increased and background subtraction is feasible. The natural calcium concentration of sea-water enhances the DASA-A1 peak height; calcium should therefore be added to fresh water to enhance the determination. The method is proposed in particular for the determination of A1 on board oceanographic vessels. There is no need to purge samples, noise due to vibrations of motions of the ship during scanning is avoided, and the sensitivity is enhanced. The total analysis time can be decreased to 8-12 min per sample by using an adsorption time of 40 s. The technique has been tested s u c d u l l y for the on-board determination of Al in sea-water. Results obtained for seawater samples irradiated by ultraviolet tight were similar to those obtained using an existing fiuorimetric method.