Abstract. Since the damming of the Nile, the Rh6ne River is the main freshwater and sediment supplier to the Mediterranean Sea. We estimated for the period 1987-1996, the dissolved and particulate organic carbon (DOC and POC), dissolved inorganic carbon (DIC), and total suspended matter (

International audienceIn the oligotrophic ocean characterized by nitrate (NO − 3) depletion in surface waters, dinitrogen (N 2) fixation and dissolved organic nitrogen (DON) can represent significant nitrogen (N) sources for the ecosystem. In this study, we deployed large in situ mesocosms in New Caledonia in order to investigate (1) the contribution of N 2 fixation and DON use to primary production (PP) and particle export and (2) the fate of the freshly produced particulate organic N (PON), i.e., whether it is preferentially accumulated and recycled in the water column or exported out of the system. The mesocosms were fertilized with phosphate (PO 3− 4) in order to prevent phosphorus (P) limitation and promote N 2 fixation. The diazotrophic community was dominated by diatom–diazotroph associations (DDAs) during the first part of the experiment for 10 days (P1) followed by the unicel-lular N 2-fixing cyanobacteria UCYN-C for the last 9 days (P2) of the experiment. N 2 fixation rates averaged 9.8 ± 4.0 and 27.7 ± 8.6 nmol L −1 d −1 during P1 and P2, respectively. NO − 3 concentrations (< 0.04 µmol L −1) in the mesocosms were a negligible source of N, indicating that N 2 fixation was the main driver of new production throughout the experiment. The contribution of N 2 fixation to PP was not significantly different (p > 0.05) during P1 (9.0 ± 3.3 %) and P2 (12.6 ± 6.1 %). However, the e ratio that quantifies the efficiency of a system to export particulate organic carbon (POC export) compared to PP (e ratio = POC export / PP) was significantly higher (p < 0.05) during P2 (39.7 ± 24.9 %) than during P1 (23.9 ± 20.2 %), indicating that the production sustained by UCYN-C was more efficient at promoting C export than the production sustained by DDAs. During P1, PON was stable and the total amount of N provided by N 2 fixation (0.10 ± 0.02 µmol L −1) was not significantly different (p > 0.05) from the total amount of PON exported (0.10 ± 0.04 µmol L −1), suggesting a rapid and probably direct export of the recently fixed N 2 by the DDAs. During P2, both PON concentrations and PON export increased in the mesocosms by a factor 1.5–2. Unlike in P1, this PON production was not totally explained by the new N provided by N 2 fixation. The use of DON, whose concentrations decreased significantly (p < 0.05) from 5.3 ± 0.5 µmol L −1 to 4.4 ± 0.5 µmol L −1 , appeared to be the missing N source. The DON consumption (∼ 0.9 µmol L −1) during P2 is higher Published by Copernicus Publications on behalf of the European Geosciences Union. 4100 H. Berthelot et al.: Dinitrogen fixation and dissolved organic nitrogen fueled primary production than the total amount of new N brought by N 2 fixation (∼ 0.25 µmol L −1) during the same period. These results suggest that while DDAs mainly rely on N 2 fixation for their N requirements, both N 2 fixation and DON can be significant N sources for primary production and particulate export following UCYN-C blooms in the New Caledonia lagoon and by extension in the N-limited oceans where similar events ...

No abstract

No abstract

Abstract. Organic molecular composition of marine aerosol samples collected during the MALINA cruise in the Arctic Ocean was investigated by gas chromatography/mass spectrometry. More than 110 individual organic compounds were determined in the samples and were grouped into different compound classes based on the functionality and sources. The concentrations of total quantified organics ranged from 7.3 to 185 ng m −3 (mean 47.6 ng m −3 ), accounting for 1.8-11.0 % (4.8 %) of organic carbon in the marine aerosols. Primary saccharides were found to be dominant organic compound class, followed by secondary organic aerosol (SOA) tracers formed from the oxidation of biogenic volatile organic compounds (VOCs) such as isoprene, α-pinene and β-caryophyllene. Mannitol, the specific tracer for airborne fungal spores, was detected as the most abundant organic species in the samples with a concentration range of 0.052-53.3 ng m −3 (9.2 ng m −3 ), followed by glucose, arabitol, and the isoprene oxidation products of 2-methyltetrols. Biomass burning tracers such as levoglucosan are evident in all samples with trace levels. On the basis of the tracer-based method for the estimation of fungal-spore OC and biogenic secondary organic carbon (SOC), we estimate that an average of 10.7 % (up to 26.2 %) of the OC in the marine aerosols was due to the contribution of fungal spores, followed by the contribution of isoprene SOC (mean 3.8 %) and α-pinene SOC (2.9 %). In contrast, only 0.19 % of the OC was due to the photooxidation of β-caryophyllene. This study indicates that primary organic aerosols from biogenic emissions, both from long-range transport of mid-latitude aerosols and from sea-to-air emission of marine organics, as well as secondary organic aerosols formed from the photooxidation of biogenic VOCs are important factors controlling the organic chemical composition of marine aerosols in the Arctic Ocean.

(350) could be determined. By contrast, the spectral slope of CDOM absorption (S CDOM ) was significantly higher (0.023 ± 0.003 nm −1 ) in summer than in fall and winter periods (0.017 ± 0.002 nm −1 ), reflecting either CDOM photobleaching or production in surface waters during stratified sunny periods. The CDOM fluorescence, assessed through excitation emission matrices (EEMs), was dominated by protein-like component (peak T; 1.30-21.94 QSU) and marine humic-like component (peak M; 0.55-5.82 QSU), while terrestrial humic-like fluorescence (peak C; 0.34-2.99 QSU) remained very low. This reflected a dominance of relatively fresh material from biological origin within the CDOM fluorescent pool. At the end of summer, surface CDOM fluorescence was very low and strongly blue shifted, reinforcing the hypothesis of CDOM photobleaching. Our results suggested that unusual RhôneCorrespondence to: R. Sempéré (sempere@univmed.fr) River plume eastward intrusion events might reach Marseilles Bay within 2-3 days and induce local phytoplankton blooms and subsequent fluorescent CDOM production (peaks M and T) without adding terrestrial fluorescence signatures (peaks C and A). Besides Rhône River plumes, mixing events of the entire water column injected relative aged (peaks C and M) CDOM from the bottom into the surface and thus appeared also as an important source of CDOM in surface waters of the Marseilles Bay. Therefore, the assessment of CDOM optical properties, within the hydrological context, pointed out several biotic (in situ biological production, biological production within Rhône River plumes) and abiotic (photobleaching, mixing) factors controlling CDOM transport, production and removal in this highly urbanized coastal area.

No abstract

[1] We investigated the penetration of solar ultraviolet radiation (UVR) in the surface waters of the south east Pacific (08 -35°S, 142 -73°W) from October to December 2004 during the BIOSOPE cruise. In the hyper-oligotrophic waters of the South Pacific Gyre (near Easter Island), diffuse attenuation coefficients for downward irradiance, K d (l), at 305 nm (UV-B), 325, 340 and 380 nm (UV-A) were 0.083, 0.055, 0.039 and 0.021 m À1 , respectively. The corresponding 10% irradiance depths, Z 10% (l), were 28, 42, 59 and 110 m, respectively. These UVR penetrations are the highest ever reported for oceanic waters and are equal to those measured in the clearest fresh waters. UV-extended inherent optical property (IOP) and radiative transfer (RT) models allowed reliable estimations of K d (l) with the Case 1 water assumption when two values of chromophoric dissolved organic matter (CDOM) absorption spectral slope coefficient (S) were used, i.e. 0.017 nm À1 at 325, 340 and 380 nm, and 0.023 nm À1 at 305 nm.