26 research outputs found

    Carbohydrates in the North Sea during spring blooms of <i>Phaeocystis</i>: a specific fingerprint

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    Regional and temporal variation in the composition of water-soluble carbohydrates from Phaeocystis colonies sampled in the southern North Sea was small during spring 1994, except for a high variability in the contribution of glucose. Glucose is universally present in storage products of microalgae; the relative constancy of the carbohydrate pattern of the other monosaccharides suggests that these are part of the more refractory colony mucus. In all Phaeocystis samples arabinose dominated, followed by xylose (Belgian coast) or galactose and mannose (Dutch coast). Rhamnose, glucuronate and O-methylated sugars were present in lower amounts. The latter, always present in samples containing Phaeocystis, may be typical for North Sea strains. The sugar patterns we report here differ from those presented in the literature concerning Phaeocystis-derived material, and also from the sugar fingerprint in the preceding diatom bloom. The Phaeocystis mucus apparently behaves as particulate matter since it was retained on filters of over 1 um. This characteristic together with its refractory nature, typical of 'transparent exopolymer particles' (TEPs), must have consequences for the heterotrophic microbial community in terms of adherence and substrate availability

    Current understanding of Phaeocystis ecology and biogeochemistry, and perspectives for future research

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    The phytoplankton genus Phaeocystis has well-documented, spatially and temporally extensive blooms of gelatinous colonies; these are associated with release of copious amounts of dimethyl sulphide (an important climate-cooling aerosol) and alterations of material flows among trophic levels and export from the upper ocean. A potentially salient property of the importance of Phaeocystis in the marine ecosystem is its physiological capability to transform between solitary cell and gelatinous colonial life cycle stages, a process that changes organism biovolume by 6–9 orders of magnitude, and which appears to be activated or stimulated under certain circumstances by chemical communication. Both life-cycle stages can exhibit rapid, phased ultradian growth. The colony skin apparently confers protection against, or at least reduces losses to, smaller zooplankton grazers and perhaps viruses. There are indications that Phaeocystis utilizes chemistry and/or changes in size as defenses against predation, and its ability to create refuges from biological attack is known to stabilize predator–prey dynamics in model systems. Thus the life cycle form in which it occurs, and particularly associated interactions with viruses, determines whether Phaeocystis production flows through the traditional “great fisheries” food chain, the more regenerative microbial food web, or is exported from the mixed layer of the ocean. Despite this plethora of information regarding the physiological ecology of Phaeocystis, fundamental interactions between life history traits and system ecology are poorly understood. Research summarized here, and described in the various papers in this special issue, derives from a central question: how do physical (light, temperature, particle distributions, hydrodynamics), chemical (nutrient resources, infochemistry, allelopathy), biological (grazers, viruses, bacteria, other phytoplankton), and self-organizational mechanisms (stability, indirect effects) interact with life-cycle transformations of Phaeocystis to mediate ecosystem patterns of trophic structure, biodiversity, and biogeochemical fluxes? Ultimately the goal is to understand and thus predict why Phaeocystis occurs when and where it does, and the bio-feedbacks between this keystone species and the multitrophic level ecosystem.info:eu-repo/semantics/publishe

    Absorption-based algorithm of primary production for total and size-fractionated phytoplankton in coastal waters

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    Most satellite models of production have been designed and calibrated for use in the open ocean. Coastal waters are optically more complex, and the use of chlorophyll <i>a</i> (chl <i>a</i>) as a first-order predictor of primary production may lead to substantial errors due to significant quantities of coloured dissolved organic matter (CDOM) and total suspended material (TSM) within the first optical depth. We demonstrate the use of phytoplankton absorption as a proxy to estimate primary production in the coastal waters of the North Sea and Western English Channel for both total, micro- and nano+pico-phytoplankton production. The method is implemented to extrapolate the absorption coefficient of phytoplankton and production at the sea surface to depth to give integrated fields of total and micro- and nano+pico-phytoplankton primary production using the peak in absorption coefficient at red wavelengths. The model is accurate to 8% in the Western English Channel and 22% in this region and the North Sea. By comparison, the accuracy of similar chl <i>a</i> based production models was >250%. The applicability of the method to autonomous optical sensors and remotely sensed aircraft data in both coastal and estuarine environments is discussed

    In vivo inhibition of nitric oxide synthesis by bisisothiouronium and bisguanidinium salts

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    Abstract The ability of two S,S'-(alkane-1,ω-diyl) bisisothiouronium dibromides, three N,N'-(alkane-1,ω-diyl) bis guanidinium dinitrates and N,N'-bis (3-guanidinopropyl)piperazine dinitrate to inhibit constitutive (i.e. endothelial and neuronal forms) and inducible forms of nitric oxide synthases has been evaluated in vivo. These compounds, synthesized by two of us (J.C.L. and C.S.), have been tested in vivo; they were administered simultaneously with an irritant (carrageenan λ) into the pleural cavity. The amount of nitrites collected 0.5 and 7 hours after this injection can be considered as an indicator of nitric oxide (NO) production. According to previous data, the first harvesting time can be related to activation of constitutive NO synthases and the second to activation of inducible NO synthases. These substances significantly inhibited nitrite production as did 2-methyl-2-thiopseudourea sulphate, previously described as a potent inhibitor of NO synthases and considered as the reference compound. The inhibiting effect varied according to the chemical structure of the compounds. Results were significantly different from controls at 0.5 h only with the S,S'-(octane-1,8-diyl) bisisothiouronium dibromide and the S,S'(nonane-1,9-diyl) bisisothiouronium dibromide at the highest concentration, N,N'-(heptane-1,7-diyl) bisguanidinium dinitrate and N,N'-bis (3-guanidinopropyl)piperazine dinitrate. At 7 h, all the results were significantly different from controls, with a major effect observed with N,N'-(heptane-1,7-diyl) bisguanidinium dinitrate. The most active substances exerted similar effects to the reference substance
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