A comparative study of mercury contamination in the Tagus estuary (Portugal) and major French estuaries (Gironde,Loire, Rhône)

Concentrations of mercury were determined for the waters, suspended matter and sediments of the Tagus and of major French estuaries.The Tagus estuary is one of the most contaminated by mercury derived from the outfalls of a chloralkali plant and from other industrial sources. In deposited sediments the median level, 1·0 μg Hg g^?1, is twenty times higher than the natural background and Hg contents depend on the sediment grain-size, age and the distance from waste-outfalls. Suspended matter is more regularly and highly contaminated (median value: 4·5 μg Hg g^?1). In the French estuaries Hg levels in the suspended material decrease with salinity due to dilution and/or remobilization processes. In June 1982, in the Loire estuary, high values of Hg are observed in the middle estuary and attributed to urban and industrial sources.In the Tagus estuary, the general distribution of total dissolved Hg confirms the contamination: it increases seaward from 10 ng 1^?1 in the river to 80 ng 1^?1 in the estuary outlet. The dissolved Hg is almost totally organic in the river, inorganic in the middle estuary due to inorganic Hg effluents and again organic in the lower estuary. This variation is related to the dissolved organic carbon values. The dissolved Hg levels in the Loire Estuary (5–300 ng 1^?1) are much higher than in the Gironde estuary (3–6 ng 1^?1) and of the same order as those observed in the Tagus estuary.     

Phytoplankton spring bloom of the Gironde plume waters in the Bay of Biscay: early phosphorus limitation and food-web consequences

During the spring 1995 (2–25 May), a cruise was carried on the RV Poseidon (Germany) on the continental shelf of the south Bay of Biscay. The objective was a comprehensive study of the planktonic food web within the Gironde plume waters. In these waters phosphate was present at very low concentrations (undetectable to < 0.1 μmol.L⁻¹), whereas nitrate, silicate and ammonium concentrations were much higher (several μmol·L⁻¹ for nitrate and silicate and 0.5 to 1.0 μmol·L⁻¹ for ammonium). The size distribution of the phytoplankton biomass (estimated from chlorophyll a measurements by high performance liquid chromatography) and primary production (measured by ¹⁴C in situ method) showed a great proportion of small (40 to 70 % < 3 μm) and active autotrophic cells (growth rates estimated from 0.4 to 0.8 d⁻¹ for the entire euphotic layer). Considering the very high values of NO₃-N:PO₄-P ratios and the high C:P and N:P ratios for the particulate organic matter, it is suggested that an early phosphorus depletion limits the spring bloom phytoplankton and particularly the new production (nitrate uptake coming from the Gironde waters).From these results and other simultaneous observations on the heterotrophic processes (such as grazing of microzooplankton), we can conclude that the planktonic food web would be close to a maintenance system as defined by Platt et al. The possible generalisation of these results for each spring is discussed with respect to the scarcity of previous and reliable phosphate data.     

Changes in biomass structure and trophic status of the plankton communities in a highly dynamic ecosystem (Gulf of Venice,Northern Adriatic Sea)

The changes in the plankton biomass structure in relation to nutrient inputs were studied in the Gulf of Venice (Northern Adriatic Sea), an area characterized by a very marked trophic state variability. The investigation was carried out at two stations, in March, May and July 2005 and 2006, considering the whole water column. The size structure (from picoplankton to mesozooplankton) of both autotrophs and heterotrophs was analysed. Signals of diluted waters and nutrient inputs were more marked in 2005 than in 2006. In 2005, the total plankton biomass was almost double (87 ± 37 μg·C·l^?1) that in 2006 (44 ± 26 μg·C·l^?1). The variations were determined mainly by phytoplankton, with a 70% decrease, and a shift from a community dominated by microphytoplankton (49 ± 12%) in 2005 to one dominated by bacteria (43 ± 11%) in 2006 was observed. The relationship between the heterotrophic (H) and autotrophic (A) biomass indicated a rapid decline of the H/A ratio with increasing phytoplankton biomass. This study, although temporally limited, is consistent with the results reported for other marine environments and it seems to confirm the importance of nutrient inputs in structuring the biomass of plankton community.     

Plankton distribution and vertical flux of biogenic matter during high summer stratification in the Krka estuary (Eastern Adriatic)

The aim of this study was to investigate phytoplankton abundance, composition and vertical export in the highly stratified Krka estuary, Croatia. The estuary is stratified throughout the year, and an interface between fresh- and brackish water plays an important role in production and degradation of biogenic matter. Vertical export of particulate organic carbon (POC), phytoplankton carbon (PPC) and faecal pellet carbon (FPC) was studied by deploying sediment traps in the middle and lower reach of the estuary and in the adjacent coastal zone. Zooplankton faecal pellet (FP) production experiments were conducted to provide additional information on the potential contribution of FP to the total carbon flux. High suspended concentrations of POC, chlorophyll a and phytoplankton was found in the lower reaches of the Krka estuary, adjacent to a source of anthropogenic eutrophication. The fraction of organic detritus to the total POC flux was 61–69% inside the estuary but only 7% at the marine station. This indicates that the primary producers in the surface layer of the Krka estuary are decomposed in and below the interface and then settle as detritus to the bottom. Low sedimentation rates in the coastal zone outside the estuary revealed that the eutrophication does not spread out of the estuary. Mesozooplankton played a modest role in vertical flux regulation, due to their low abundance and dominance of smaller forms as well as low faecal pellet production rates. It is concluded that processes taking place at the freshwater-seawater interface are of major importance for the vertical carbon flux in the investigated area.     

Ten-year observation of the Gironde tributary fluvial system: fluxes of suspended matter, particulate organic carbon and cadmium

A program of long-term observation of suspended solids (TSS), particulate organic carbon (POC) and cadmium transported into the Gironde estuary (France) by its major tributaries has been carried out between 1990 and 1999. This decade included contrasting hydrologic cycles and appears representative of a much longer period (1959–1999). The Garonne and the Dordogne river systems are the main tributaries of the Gironde estuary and derive their waters from drainage basins with different geological, industrial and agricultural features. To better understand their respective contributions, they have been observed separately and compared. Water and TSS fluxes of the Garonne River show greater temporal variations and discharge is more related to the hydrology of the drainage basin (e.g. wet/dry years, local flood events etc.). As POC and particulate Cd concentrations in suspended matter are much less variable than turbidity, their fluxes are mainly controlled by the TSS transport. A major part of annual fluxes of TSS and associated pollutants may occur within few flood days (depending on various parameters, e.g. intensity, duration, season, etc.), and also the succession of dry and wet years has an important influence on annual fluxes. The presented data allow calculating fluvial inputs into the Gironde as the sum of fluxes transported by its major tributaries, the Garonne and the Dordogne river systems. Mean annual fluxes into the Gironde observed in 1990–1999 are about 34×10⁹ m³ year⁻¹ for river water, 3.24×10⁶ t year⁻¹ for suspended solids (TSS) and 9.88×10⁹ mol year⁻¹ for particulate organic carbon (POC). Generally, these fluxes are dominated by the contributions of the Garonne River. However, in dry years, the mean contribution of the Dordogne river system (including Dronne and Isle rivers) to the POC input into the estuary exceeded that of the Garonne. This reflects significant differences in vegetation and soil due to natural properties and land management of the basins. Mean Cd fluxes into the estuary are about 110×10³ mol year⁻¹ of which 19.6×10³ mol year⁻¹ are transported in the dissolved and 90.8×10³ mol year⁻¹ in the particulate phases, respectively. In 1991 (dry year), the net (dissolved) Cd flux towards the ocean exceeded the gross fluvial input of total Cd, suggesting the release of Cd from an important stock in the maximum turbidity zone (MTZ) or the fluid mud of the Gironde estuary.     

Mercury in the Southern North Sea and Scheldt estuary

Dissolved and particulate mercury and methylmercury concentrations were determined in the Southern Bight of the North Sea and the Scheldt estuary in the period 1991–1999. Mercury and methylmercury concentrations are higher before 1995 than after 1995, especially in the fluvial part.The North Sea: In the offshore stations, dissolved Hg concentrations are generally higher in winter than in summer while the reverse is true for particulate Hg K_D values (K_D=the concentration of particulate Hg (Hg_P in pmol kg⁻¹) divided by the concentration of dissolved Hg (Hg_D in pmol l⁻¹)) range from 100,000 to 1000,000 l kg⁻¹. Dissolved methylmercury concentrations vary from 0.05 to 0.25 pmol l⁻¹ in summer and from d.l. to 0.23 pmol l⁻¹ in winter and particulate methylmercury concentrations from 1.8 to 36 pmol g⁻¹ in summer and from 0.9 to 21 pmol g⁻¹ in winter. The K_D ranges from 9,000 to 219,000 l kg⁻¹.The Scheldt estuary: In winter, dissolved Hg concentrations are elevated in the upper estuary, decrease exponentially in the low salinity range followed by a very slow decrease towards the mouth. In summer, they are low in the fluvial part, increase in the low salinity range or in the mid-estuary and sometimes show an increase in the lower estuary. Particulate Hg concentrations do not show any seasonal trend.Dissolved MMHg concentrations are much lower in winter, when maximum concentrations are found in the upper estuary, than in summer. In summer, the MMHg concentrations are low at low salinity, they show a first increase in the salinity range from 3 to 12, a decrease in the mid-estuary and a second increase in the lower estuary.The highest particulate MMHg concentrations are found in the upper estuary, while in the lower estuary generally lower and more constant values are observed. The ratio of dissolved MMHg to dissolved Hg (cruise averages between 1.3% and 20%), is higher than the ratio of particulate MMHg to particulate Hg (cruise averages of 0.27–0.90%). The K_D values for MMHg are lower in the summer (30,000–65,000) than in autumn and winter (77,000–114,000).The Scheldt river: In the fluvial part of the Scheldt, dissolved increases in the most upstream stations, while particulate Hg shows no particular pattern. Dissolved MMHg ranges from 0.1 to 0.39 pmol l⁻¹ and particulate MMHg from 3.1 to 43.5 pmol g⁻¹. The MMHg concentrations are comparable to those found in the estuary and no seasonal variations could be observed.     

Chemical composition of corals in Saudi Red Sea Coast

Three species of corals Stylophora pistillata, Lobophyllia corymbosa and Echinopora gemmacea were collected from Sharm Obhur to study their chemical composition. This information was important in the investigation of their metabolic pathways and their mode of feeding. The concentrations of amino acids in these species were 9.37, 21.35 and 3.09 mg·g⁻¹ dry weight of coral respectively. Plant pigments were highest in E. gemmacea followed by S. pistillata and then by L. corymbosa. Lipid concentrations in S. pistillata, L. corymbosa and E. gemmacea were 1.90, 8.58 and 1.32 mg·g⁻¹ of total coral respectively. The fatty acid methyl esters were analyzed in these species and the most abundant saturated acids were 16:0 and 18:0, while unsaturated acids included 16:1, 18:1 and 19:3. The carbohydrate concentrations were 559, 425 and 859 μg·g⁻¹ of total coral dry weight. Residual matter was 42.5, 32.8 and 41.39 per cent by weight of total coral. These data suggest a greater reliance on autotrophic feeding in E. gemmacea and S. pistillata and mostly heterotrophic feeding in L. corymbosa.     

Apports de nutriments et développement phytoplanctonique en baie de Seine

As part of the Programme National d'Océanographie Côtière, the nutrient dynamics of the Bay of Seine were studied between 1992 and 1994 in order to complement work on ecological modelling. Firstly, the River Seine's nutrient fluxes were established: 80 000–130 000 t a⁻¹ of dissolved inorganic nitrogen, 6 400–8 4001 a⁻¹ of dissolved phosphorus and 20 000–77 000 t a⁻¹ of dissolved silicium. Estuarine processes were taken into account. Consequences of nutrient loading for the bay were then evaluated at the pelagic level (nutrient and chlorophyll enrichments) and the benthic level (distribution of various phosphorus fractions in superficial sediments). The large continental inputs always induce concentration gradients in the water from the mouth of the river to the northwest of the bay. The northward spreading of fine particulate matter controls the distribution of adsorbed phosphate and iron-aluminium bound phosphate in sediments. In contrast, calcium bound phosphate, the main fraction in sediments, is not affected by river inputs. Organic phosphorus in sediments is related to phytoplankton blooms, with increasing concentrations during productive periods; afterwards the fast recycling prevents sedimentary accumulation. The nutrient depletions observed beyond the turbid plume during spring 1992 enabled the calculation of nutrient uptake rates, and the comparison of these rates with phytoplankton biomass (chlorophyll a + phaeopigments). Ratios of nutrient consumption to pigment concentration were estimated at 1 μmol μg⁻¹ for nitrogen, 0.05 for phosphorus and 0.5 for silicate. These values, as N/P and Si/N uptake ratios (respectively 17.5 and 0.4), were similar to usual values.     

Response of Sedimentary Nucleic Acids to Benthic Disturbance in the Central Indian Basin

Information on the response of nucleic acids (i.e., DNA and RNA) to simulated benthic disturbance was obtained from samples collected from eight sediment cores (0–10 cm) located in the Central Indian Basin (CIB). In general the total sedimentary DNA (DNA) increased with depth (from 380.09 to 408.99 μg·g^?1), while total sedimentary RNA (RNA) decreased (from 878.13 to 484.16 μg·g^?1). Following the simulated benthic disturbance brought about by the benthic hydraulic disturber, DNA decreased by 10% along the disturbed track while the RNA increased by around 75%. The RNA/DNA ratio decreased nearly 10%. However, the ratio doubled along the disturbed track suggesting that the activity was stimulated at molecular level following artif icial disturbance. The nucleic acid ratio thus shows that the CIB sediments are metabolically active, and with disturbance the activity tends to increase further.     

Trace metals in the Göta river estuary

The concentrations of the trace metals Cd, Cu, Fe, Ni, Pb and Zn in the Göta River estuary have been investigated. The following metal fractions have been determined: acid-leachable, dissolved, labile and particulate.The estuary represents a salt wedge type estuary and is situated in a densely populated region of Sweden. The metal concentrations found for the dissolved fraction is in the range of what can be considered as background levels for freshwater. It is difficult to evaluate any estuarine processes other than conservative mixing for Cd, Cu, Ni and Zn. The dissolved levels in the freshwater end member are Cd, 9–25 ngl^?1; Cu, 1·1–1·4 μgl^?1; Fe, 20–75 μg l^?1: Ni, 0·7–0·9 μg l^?1: Pb 0·09–0·2 μg l^?1; and Zn, 6–7 μg l^?1:The results from the acid-leachable fraction show that at high suspended load the particles sediment in the river mouth. The trace metal levels in this fraction are subject to large variations.     

Dissolved chromium in the St. Lawrence estuary

A study of dissolved chromium in the St. Lawrence estuary and Gulf of St. Lawrence has been carried out. A chromium concentration of 0·7 μg l^?1 was found in the St. Lawrence River. In the turbidity maximum of the upper estuary, chromium is removed from solution onto fine-grained resuspended sediments and internally produced organic-rich floccules. A simple flux calculation shows that these processes remove ～50% of the total dissolved chromium input of the river. At salinities greater than 5‰ dissolved chromium mixes conservatively.     

An electrochemical study of the speciation of copper,zinc and iron in two estuaries in England

The organic speciation of copper, iron and zinc in estuarine waters is studied using electrochemical techniques. Complexing capacities for copper and zinc were determined by cathodic stripping voltammetry (CSV) of their complexes with respectively catechol and amino pyrrolidine dithiocarbamate (APDC). Iron speciation was studied by CSV measurements of dissolved iron before (‘free iron’) and after acidification and UV-irradiation (‘total iron’) of the filtered samples. Complexing capacities of copper were found to vary between 1·4 and 5 × 10⁻⁷m with conditional stability constants, logK′_CuL, between 9·2 and 10·3 in the Tamar estuary. Complexing capacities of zinc were less at between 0·4 and 1·6 × 10⁻⁷m with values for logK′_ZnL between 8·1 and 9·4. Copper complexing capacities generally decreased with increasing salinity, and variations in the results were related to high concentrations of suspended material. Similar variations in the dissolved vanadium concentrations suggested that part of this element was associated with colloidal material. The total dissolved iron concentration in samples from the River Ribble decreased from 10⁻⁶m at low salinity to 10⁻⁷m at high salinity, but the free iron concentration was found to decrease from 8 to 3 × 10⁻⁸m over the same salinity range, which may be compared with the calculated solubility of iron in seawater of 2 × 10⁻⁸m. Comparative experiments showed that on average about 24% of the non-labile iron fraction was stabilized by organic material, the rest being composed of inorganic colloidal material.     

Seasonal variability in the kinetics of Cu,Pb, Cd and Hg accumulation by macroalgae

Here it is demonstrated that both Porphyra spp. and Enteromorpha spp. of macro-algae display similar and very marked seasonal variations in their concentration factor (CF) of Cu, Pb, Cd and Hg in field conditions. The CF variations are specific for each metal and reproducible over several years. The way variations in the biological activity affect the equilibrium and kinetics of the interaction between trace metals and live algae was studied in vitro. Natural seawater was used as the culture medium. Voltammetry was used for the determination of natural organic ligands and trace metals except Hg, which was determined by mercury cold vapour after on-line pre-concentration. Titrations with the relevant metal demonstrated that the maximum binding capacity of the algae was not significantly dependent on the season for Pb (ca. 100 μmol g_{dry algae}⁻¹), Cd (ca. 50 μmol g⁻¹) and Hg (80–100 μmol g⁻¹). Marked seasonal variations were observed for Cu (ca. 40 μmol g⁻¹ in January; 70 μmol g⁻¹ in May; and 100 μmol g⁻¹ in August). The conditional stability constants of metal–algae complexation sites were seasonally independent and similar for both algae: logK_MS′=8.5±0.3 (Cu), 5.6±0.2 (Pb), 5.3±0.2 (Cd) and 18.0±0.3 (Hg). Exudates with a strong Cu complexing capacity (logK′_CuL=12.47±0.06) were determined in cultures with added Cu, Pb or Cd concentrations, and identified by cathodic stripping voltammetry (CSV) as cysteine or glutathione. All the tested metals promoted the liberation of exudates, both cysteine- and glutathione-like ligands were exuded in the presence of Cu, only cysteine-like ligands in the presence of Pb, and only glutathione-like ligands in the presence of Cd, the rise depending of the season of the year, particularly for Cu. Highest levels were produced in the presence of added Pb. When exposed to either 1- or 100-μM total dissolved metal concentrations, the metal uptake, and its rate, varied with the season and the algae.     

Hydrochemistry of the Tumen River Estuary,Sea of Japan

The hydrological and hydrochemical parameters of the Tumen River estuary were collected at 13 stations in May and October 2015. Vertical temperature, conductivity, dissolved oxygen, chlorophyll fluorescence, and turbidity profiles were obtained. Water was sampled from the surface and bottom layer. The water samples were analyzed for major ions, pH, salinity, concentrations of dissolved oxygen, major nutrients, dissolved organic carbon, humic matter, and δ¹⁸О and δD isotopes. This estuary is attributed to microtidal type with a flushing time of about 10 h. A phytoplakton bloom occurred in the top layer of the estuary. For surface horizons, the hydrochemical parameters show a linear correlation with salinity. In the bottom horizons, all these parameters, except for major ions and δ¹⁸О and δD isotopes, reveal substantial nonconservative behavior. The nonconservative behavior of the hydrochemical parameters in the bottom waters was mainly caused by degradation of the phytoplankton biomass at the water/sediment interface. Hypoxic conditions were established in the bottom waters of the estuary in May.     

Coprostanol levels and organic enrichment in sediments of the Bilbao estuary (north of Spain)

An assessment was made of the distribution of the faecal sterol coprostanol (COP) in sediments in the Bilbao estuary. Concentrations of COP ranged from 135.15 to 10.77 μg g⁻¹ dry weight, from the inner to the open estuary, with a mean value of 51.43 μg g⁻¹; the highest concentrations were found near the mouths of several tribularies flowing into the estuary. Comparisons with other published values indicate that sediments from the Bilbao estuary are affected by sewage pollution in a similar degree to that reported for other estuaries in the world. Organic enrichment and anaerobic sediment conditions prevail in three-fourths of its watercourse bed. Since the spatial distribution of several organic sedimentary parameters could be clearly correlated with COP levels, we can conclude the existence of major pollution by the addition of untreated sewage, coming from mainly domestic sources. The implementation of a sewerage treatment plan by the local water authority needs the monitoring of reliable sewage tracers, such as faccal sterols, to assess the effectiveness of the plan in reducing the effects of pollution.     

The nitrogen isotopic composition of dissolved nitrate in the Yangtze River (Changjiang) estuary,China

The nitrogen isotopic composition of dissolved nitrate (δ¹⁵N-NO₃⁻) in surface water of the Yangtze River estuary was determined in four seasons of 2006. δ¹⁵N-NO₃⁻ ranged from 0.4‰ to 6.5‰ and varied with seasons and geographic regions, reflecting the dynamics of nitrogen cycling in the estuarine ecosystem. δ¹⁵N-NO₃⁻ was markedly lower in February than in other seasons and exhibited conservative mixing, which was probably attributed to the NO₃⁻ being sourced from the atmospheric deposition and agricultural fertilizer. In the upper estuary, the influence of riverine inputs was important during all surveys. In the turbidity maximum zone, nitrification was found with nitrate depleted in ¹⁵N in May, whereas denitrification resulting in heavy δ¹⁵N-NO₃⁻ played an important role in August. More enriched δ¹⁵N-NO₃⁻ values coinciding with losses of nitrate concentrations based on the conservative mixing model were found in the adjacent marine area in May, and may reflect obvious phytoplankton assimilation of dissolved nitrate. In this manner, δ¹⁵N-NO₃⁻ may be a sensitive indicator of nitrogen sources and biogeochemical processing existing in this estuary in conjunction with the variations of dissolved nitrate and other environmental factors.     

Seasonal variations of dissolved and particulate copper species in estuarine waters

This one-year survey conducted in the macrotidal estuary of Penzé (Brittany, Western part of the Channel, France) was aimed at examining the variations of the various dissolved and particulate copper species. Ten field stations along the whole freshwater–seawater mixing zone were sampled each month. Different biogeochemical parameters (SPM, chl-a, pH and DOC) were also measured. The levels in total dissolved and total particulate copper ranged from 1.8 to 9.5 nM and from 5 to 98 μg g⁻¹, respectively; such amounts are indicative of a pollution-free system. Extractable C₁₈ copper (non-polar hydrophobic organic copper species), in winter and spring, accounted for 30–40% of the total dissolved copper. In summer, this contribution rapidly rose to 60% in the salinity range 20–30; over the same period of time, total particulate copper decreased. The change in dissolved copper speciation and the lowering of particulate copper concentrations were attributed to the release of strong organic ligands by phytoplankton. Our field data evidenced a highly variable behaviour for the various copper species over the seasonal cycle, and then led us to identify the following mechanisms: (i) metal desorption from organic river-flown particles (winter and spring), (ii) metal desorption from resuspended sediment in the upstream section (summer), (iii) competition between particles, non-extractable C₁₈ organic ligands and phytoplankton-released extractable C₁₈ organic ligands to complex copper in the downstream section (summer), and (iv) removal of non-extractable C₁₈ organic copper by adsorption (autumn). Dissolved copper species fluxes were assessed: most of metal inputs to the estuary (60–74%) corresponded to non-extractable C₁₈ organic copper. Winter and spring metal output fluxes were mainly constituted of non-extractable C₁₈ organic complexes; on the other hand, extractable C₁₈ organic complexes were predominant in summer and autumn output fluxes.     

Low reproductive success for copepods during a bloom of the non‐aldehyde‐producing diatom Cerataulina pelagica in the North Adriatic Sea

Egg production rates and/or hatching success in the copepods Acartia clausi, Calanus helgolandicus and Temora longicornis were negatively affected by a late spring (May–June 2003) phytoplankton bloom in the North Adriatic Sea, dominated mainly by the large diatom Cerataulina pelagica. Highest total concentrations of 3.3·10⁴ cells·ml^?1 were located in the vicinity of the Po River, which also corresponded to the area where the highest numbers of phaeophorbides were measured (0.779, 0.528 and 0.419 μg·l^?1, respectively, compared to an average of the remaining stations of 0.183 ± 0.049 SD), suggesting some grazing on the bloom. Phytoplankton biomass in terms of carbon was dominated by diatoms, representing on average 42% of total phytoplankton carbon and more than 80% at several stations. Cerataulina pelagica, Cyclotella spp., Chaetoceros spp. and small unidentified centric diatoms dominated the diatom community numerically but C. pelagica was by far the dominant diatom in terms of carbon due to its large cell size. This species represented more than 60% of the diatom biomass at nine of the 14 stations sampled, and was absent only at one station, which was the most offshore station sampled during the cruise. Although polyunsaturated aldehydes (PUAs) were not detected, other oxylipins which are hydroxy and keto derivatives of eicosapentaenoic and docosahexaenoic acids that affect copepod reproduction were found in these samples. Hence, we can attribute the negative impact of diatoms not only to PUAs, as previously believed, but also to these compounds. This is the first direct evidence of the presence of oxylipins other than PUAs in marine blooms dominated by diatoms.     

Distribution and quality of sedimentary organic matter on the Aquitanian margin (Bay of Biscay)

During the ECOFER experiment (French ECOMARGE program), surficial sediments were sampled on the Aquitanian margin with box corers and analyzed to determine the quantity and quality of organic matter. Sediments from the margin are enriched in organic carbon (mean value 1.35%) in comparison to deep-sea and shelf sediments, due to a fine grain-size sedimentation. As sedimentation rates are high, the margin appears to be an organic depocenter. Some preferential organic enrichment zones were identified in the Cap-Ferret Canyon. There is a supply of continental material from the Gironde estuary, but marine contribution seems more possible than Adour or spanish rivers. No seasonal variations of organic matter were observed at the surface of sediments, suggesting mineralization processes of labile organic matter: average organic carbon consumption was evaluated to 9.0 g C m⁻² yr⁻¹. Rapid biological mineralization processes are lower than on the Mediterranean margin, mainly related to significant differences in water temperature. The great width of the canyon, its distance from the continent, and the current circulation pattern prevent any precise recording of the variable organic inputs to the sediment and favor nepheloı̈d transport, resuspension and shelf break processes, which wipe out any print of fresh material input. An organic carbon budget indicates that an equilibrium between organic inputs and organic mineralization+accumulation is not obtainable. The supply of suspended matter could have been minor during the year in question, and sedimentation rates are still imprecise.