Physical-chemical constraints on cyanobacterial growth in the Oceans
Identifieur interne : 00C666 ( Main/Exploration ); précédent : 00C665; suivant : 00C667Physical-chemical constraints on cyanobacterial growth in the Oceans
Auteurs : H. W. Paerl [États-Unis]Source :
- Bulletin de l'Institut océanographique : (Monaco) [ 0304-5722 ] ; 1999.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Océan.
English descriptors
- KwdEn :
Abstract
Cyanobacteria are significant and at times dominant contributors to estuarine, coastal and open ocean primary production and fixed nitrogen inputs. CO2 and N2 fixation can be controlled by single or combined nutrient supplies, depending on the influence of external vs. internal inputs. Nitrogen limitation characterizes much of the world's oceanic surface waters, providing a vast niche for cyanobacteria capable of N2 fixation. The filamentous planktonic N2 fixers, Trichodesmium and Richelia (endosymbiont in the diatom Rhizosolenia) can form large (< 100's of km2) surface blooms in nutrient-deplete, oligotrophic open ocean waters. Here, the availability of iron (Fe), a cofactor in the N2 fixing enzyme complex nitrogenase, may control N2 fixation, as shown subtropical W. Atlantic and Caribbean waters. The picoplanktonic (< 5 μm) genera Synechococcus, Synechocystis, and Prochlorococcus are important (i.e., 20 to > 50%) contributors to phytoplankton productivity and biomass. These non N2 fixers rely on small size (i.e., high surface to volume ratio) and efficient light harvesting abilities, to optimize growth in poorly-illuminated, nutrient-rich deep waters. Marine cyanobacteria exhibit various morphological, physiological, and ecological strategies aimed at co-optimizing diazotrophy, photosynthesis and nutrient (N, P, Fe) sequestration. These include; buoyancy regulation to facilitate access to near-surface sunlight (energy) and nutrient-rich deeper water, aggregation as colonies supporting nutrient-exchanging consortial interactions with microheterotrophs and invertebrate grazers, endosymbioses, intracellular nitrogen and phosphorus storage, heterotrophic and photoheterotrophic capabilities. Certain cyanobacterial genera can exploit nutrient-enriched estuaries and seas (e.g. Baltic), sometimes as persistent nuisance (i.e. hypoxia/anoxia-generating, toxic) blooms. If N2 fixing cyanobacteria predominate as planktonic blooms (Nodularia, Aphanizomenon) or benthic mats (Lyngbya, Oscillatoria), or if high rates of external N loading occur, N+P co-limitation or exclusive P limitation may dominate. In non-N2 fixing communities, Fe may synergistically interact with combined N, especially NO3-, to enhance growth. Increasing anthropogenic N and Fe enrichment (runoff, atmospheric deposition, groundwater) supports large-scale eutrophication which, in addition to degrading water quality, affects air-water CO2 fluxes, oceanic C, N and other nutrient budgets.
Affiliations:
- États-Unis
- Caroline du Nord
- Chapel Hill (Caroline du Nord)
- Université de Caroline du Nord à Chapel Hill
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Le document en format XML
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<keywords scheme="Pascal" xml:lang="fr"><term>Cyanobacteria</term>
<term>Bactérioplancton</term>
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<term>Facteur milieu</term>
<term>Propriété physicochimique</term>
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<front><div type="abstract" xml:lang="en">Cyanobacteria are significant and at times dominant contributors to estuarine, coastal and open ocean primary production and fixed nitrogen inputs. CO<sub>2</sub>
and N<sub>2</sub>
fixation can be controlled by single or combined nutrient supplies, depending on the influence of external vs. internal inputs. Nitrogen limitation characterizes much of the world's oceanic surface waters, providing a vast niche for cyanobacteria capable of N<sub>2</sub>
fixation. The filamentous planktonic N<sub>2</sub>
fixers, Trichodesmium and Richelia (endosymbiont in the diatom Rhizosolenia) can form large (< 100's of km<sup>2</sup>
) surface blooms in nutrient-deplete, oligotrophic open ocean waters. Here, the availability of iron (Fe), a cofactor in the N<sub>2</sub>
fixing enzyme complex nitrogenase, may control N<sub>2</sub>
fixation, as shown subtropical W. Atlantic and Caribbean waters. The picoplanktonic (< 5 μm) genera Synechococcus, Synechocystis, and Prochlorococcus are important (i.e., 20 to > 50%) contributors to phytoplankton productivity and biomass. These non N<sub>2</sub>
fixers rely on small size (i.e., high surface to volume ratio) and efficient light harvesting abilities, to optimize growth in poorly-illuminated, nutrient-rich deep waters. Marine cyanobacteria exhibit various morphological, physiological, and ecological strategies aimed at co-optimizing diazotrophy, photosynthesis and nutrient (N, P, Fe) sequestration. These include; buoyancy regulation to facilitate access to near-surface sunlight (energy) and nutrient-rich deeper water, aggregation as colonies supporting nutrient-exchanging consortial interactions with microheterotrophs and invertebrate grazers, endosymbioses, intracellular nitrogen and phosphorus storage, heterotrophic and photoheterotrophic capabilities. Certain cyanobacterial genera can exploit nutrient-enriched estuaries and seas (e.g. Baltic), sometimes as persistent nuisance (i.e. hypoxia/anoxia-generating, toxic) blooms. If N<sub>2</sub>
fixing cyanobacteria predominate as planktonic blooms (Nodularia, Aphanizomenon) or benthic mats (Lyngbya, Oscillatoria), or if high rates of external N loading occur, N+P co-limitation or exclusive P limitation may dominate. In non-N<sub>2</sub>
fixing communities, Fe may synergistically interact with combined N, especially NO<sub>3</sub>
<sup>-</sup>
, to enhance growth. Increasing anthropogenic N and Fe enrichment (runoff, atmospheric deposition, groundwater) supports large-scale eutrophication which, in addition to degrading water quality, affects air-water CO<sub>2</sub>
fluxes, oceanic C, N and other nutrient budgets.</div>
</front>
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