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Bibliographic Details
Main Authors: Blanchot, Jean, Rodier, Martine
Format: Dataset Open Access
Language:en
Published: PANGAEA 1996
Subjects:
Biogeochemical Processes in the Oceans and Fluxes; Counting by flow cytometer; CTD/Rosette; CTD-RO; Cyanobacteria; Date/Time of event; DEPTH, water; EBENE; EBENE_001; EBENE_002; EBENE_003; EBENE_004; EBENE_005; EBENE_006; EBENE_007; EBENE_008; EBENE_009; EBENE_010; EBENE_011; EBENE_012; EBENE_013; EBENE_014; EBENE_015; EBENE_016; EBENE_017; EBENE_018; EBENE_019; EBENE_020; EBENE_021; EBENE_022; EBENE_023; EBENE_024; EBENE_025; EBENE_026; EBENE_027; EBENE_028; EBENE_029; EBENE_030; EBENE_031; EBENE_032; EBENE_033; EBENE_034; EBENE_035; EBENE_036; EBENE_037; EBENE_038; EBENE_039; EBENE_040; EBENE_041; EBENE_042; EBENE_043; EBENE_044; EBENE_045; EBENE_046; EBENE_047; EBENE_048; EBENE_049; EBENE_050; EBENE_051; EBENE_052; EBENE_053; EBENE_054; EBENE_055; EBENE_056; EBENE_057; EBENE_058; EBENE_059; EBENE_060; EBENE_061; EBENE_062; EBENE_063; EBENE_064; EBENE_065; EBENE_066; EBENE_067; EBENE_068; EBENE_069; EBENE_070; EBENE_071; EBENE_072; EBENE_073; EBENE_074; EBENE_075; EBENE_076; EBENE_077; EBENE_078; EBENE_079; EBENE_080; EBENE_081; EBENE_082; EBENE_083; EBENE_084; EBENE_085; EBENE_086; EBENE_087; EBENE_088; EBENE_089; EBENE_090; EBENE_091; EBENE_092; EBENE_093; EBENE_094; EBENE_095; EBENE_096; EBENE_097; EBENE_098; EBENE_099; EBENE_100; EBENE_101; EBENE_102; EBENE_103; EBENE_104; EBENE_105; EBENE_106; EBENE_107; EBENE_108; EBENE_109; EBENE_110; EBENE_111; EBENE_112; EBENE_113; EBENE_114; EBENE_115; EBENE_116; EBENE_117; EBENE_118; EBENE_119; EBENE_120; EBENE_121; EBENE_122; EBENE_123; EBENE_124; EBENE_125; EBENE_126; EBENE_127; EBENE_128; EBENE_129; EBENE_130; EBENE_131; EBENE_132; EBENE_133; EBENE_134; EBENE_135; EBENE_136; EBENE_137; EBENE_138; EBENE_139; EBENE_140; EBENE_141; EBENE_142; EBENE_143; EBENE_144; EBENE_145; Equatorial Pacific; Event label; JGOFS; Joint Global Ocean Flux Study; L Atalante; Latitude of event; Longitude of event; Microalgae; Prochlorophytes; PROOF
Online Access:https://doi.org/10.1594/PANGAEA.807552
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Table of Contents:
  • Natural populations of phytoplankton from the western tropical Pacific Ocean were analyzed by flow cytometry from a transect along 165°E between 20°S and 7°N. The abnormal hydrological situation corresponded to a weak El Niño event, with no equatorial upwelling and a marked nutrient ridge centered on 10°S. Prochlorophytes dominated numerically everywhere along the vertical, whatever the depth, in the 0-160-m layer (96% of cell abundance). Paradoxically, the highest concentrations, up to 4.4 x 10**5 cells/ml, were found in oligotrophic waters (< 0.1 µM NO3). In contrast, the highest concentrations of orange cyanobacteria and redfluorescing picoeukaryotes were observed when nitrate was present in the photic layer, i.e. around 10°S (up to 6.4 x 10**4 cells/ml and 1.3 x 10**4 cells/ml), and, to a lesser extent in the vicinity of the deep nitracline north of 8°S. Along the transect we encountered two hydrological situations, characterized by different community structures. The first one, found from 15°S to 7°N, except at 10°S, was a two-layer structure (Typical Tropical Structure, TTS) defined by a strong pycnocline in the upper 180 m and a well-marked nitracline. In this region, Prochlorococcus and picoeukaryotes co-dominated the 180-m integrated fluorescence and carbon biomass, but Prochlorococcus were the major component in the upper nitrate-depleted layer, while picoeukaryotes dominated the underlying rich layer. Inversely, Synechococcus were a relatively minor contributor to fluorescence (~4%) and phytoplankton biomass (< 1%) in comparison to the other cell types. The second structure observed in the southernmost part of the transect (20°S-16°S) was defined by the absence of a density gradient, and therefore by deep vertical mixing. In this case, the concentration of Prochlorococcus in the upper nitrate-depleted layer was reduced, whereas Synechococcus percentage contribution in the upper 180 m was significantly higher than in the TTS ( > 30% of total fluorescence and ~4% of carbon biomass). According to our results, we discuss the expected role of each phytoplankton group in the regenerated and new production. Finally, we discuss the importance of cell size as a factor in the expected roles of the different phytoplankton groups in the carbon sink.