Monthly averaged level-3 SeaWiFS chlorophyll concentration data from 1998 to 2001 are globally analyzed using Fourier's analysis to determine the main patterns of temporal variability in all parts of the world ocean. In most regions, seasonal variability dominates over interannual variability, and the timing of the yearly bloom can generally be explained by the local cycle of solar energy. The studied period was influenced by the late consequences of the very strong El Niño of 1997-98. After this major event, the recovery to normal conditions followed different patterns at different locations. Right at the equator, chlorophyll concentration was abnormally high in 1998, and then decreased, while aside from the equator, it was low in 1998, and increased later when equatorial upwelled waters spread poleward.
We investigated the effects of changes in nutrient concentrations on phytoplankton biomass and community composition during 8 field trips performed during different seasons in the southwestern coral lagoon of New Caledonia. The lagoon is characterized by spatial variation in macronutrient concentrations, with locally elevated values in the bays bordering the city of Nouméa. Low DIN:DIP (dissolved inorganic nitrogen:dissolved inorganic phosphorus) and elevated Si:DIN ratios suggest that nitrogen is the macronutrient that likely drives phytoplankton community composition. Most of the microphytoplankton groups discriminated by inverted microscopy and the picoplankton groups distinguished by flow cytometry present significant and distinct relationships with inorganic nitrogen concentrations. Picophytoplankton-dominated assemblages are replaced by microphytoplankton-dominated assemblages with increasing DIN concentrations. Within the picophytoplankton, Prochlorococcus abundance dominates in the adjacent oceanic and southern lagoon shelf sites, and assemblages shift to Synechococcus-dominated populations in the bays, with an increasing proportion of picoeukaryotic phytoplankton. Within the microplankton, 142 species of microphytoplankton were identified, mainly represented by diatoms, dinoflagellates, and coccolithophorids. Nutrient enrichment in the bays favors large diatoms at the expense of coccolithophorids and dinoflagellates, which dominate in adjacent oceanic and southern shelf waters. Therefore, although moderate, the elevated nitrogen concentrations in the bays result in increased phytoplankton biomass, accompanied by important shifts in the phytoplankton community structure.
The present study reports on observations carried out in the Tropical North Atlantic in summer and autumn 2017, documenting Sargassum aggregations using both ship-deck observations and satellite sensor observations at three resolutions (MSI-10 m, OLCI-300 m, VIIRS-750 m and MODIS-1 km). Both datasets reported that in summer, Sargassum aggregations were mainly observed off Brazil and near the Caribbean Islands, while they accumulated near the African coast in autumn. Based on in situ observations, we propose a five-class typology allowing standardisation of the description of in situ Sargassum raft shapes and sizes. The most commonly observed Sargassum raft type was windrows, but large rafts composed of a quasi-circular patch hundreds of meters wide were also observed. Satellite imagery showed that these rafts formed larger Sargassum aggregations over a wide range of scales, with smaller aggregations (of tens of m2 area) nested within larger ones (of hundreds of km2). Match-ups between different satellite sensors and in situ observations were limited for this dataset, mainly because of high cloud cover during the periods of observation. Nevertheless, comparisons between the two datasets showed that satellite sensors successfully detected Sargassum abundance and aggregation patterns consistent with in situ observations. MODIS and VIIRS sensors were better suited to describing the Sargassum aggregation distribution and dynamics at Atlantic scale, while the new sensors, OLCI and MSI, proved their ability to detect Sargassum aggregations and to describe their (sub-) mesoscale nested structure. The high variability in raft shape, size, thickness, depth and biomass density observed in situ means that caution is called for when using satellite maps of Sargassum distribution and biomass estimation. Improvements would require additional in situ and airborne observations or very high-resolution satellite imagery.
BackgroundMorphological data suggest that, unlike most other groups of marine organisms, scleractinian corals of the genus Stylophora are more diverse in the western Indian Ocean and in the Red Sea than in the central Indo-Pacific. However, the morphology of corals is often a poor predictor of their actual biodiversity: hence, we conducted a genetic survey of Stylophora corals collected in Madagascar, Okinawa, the Philippines and New Caledonia in an attempt to find out the true number of species in these various locations.ResultsA molecular phylogenetic analysis of the mitochondrial ORF and putative control region concurs with a haploweb analysis of nuclear ITS2 sequences in delimiting three species among our dataset: species A and B are found in Madagascar whereas species C occurs in Okinawa, the Philippines and New Caledonia. Comparison of ITS1 sequences from these three species with data available online suggests that species C is also found on the Great Barrier Reef, in Malaysia, in the South China Sea and in Taiwan, and that a distinct species D occurs in the Red Sea. Shallow-water morphs of species A correspond to the morphological description of Stylophora madagascarensis, species B presents the morphology of Stylophora mordax, whereas species C comprises various morphotypes including Stylophora pistillata and Stylophora mordax.ConclusionsGenetic analysis of the coral genus Stylophora reveals species boundaries that are not congruent with morphological traits. Of the four hypotheses that may explain such discrepancy (phenotypic plasticity, morphological stasis, morphological convergence, and interspecific hybridization), the first two appear likely to play a role but the fourth one is rejected since mitochondrial and nuclear markers yield congruent species delimitations. The position of the root in our molecular phylogenies suggests that the center of origin of Stylophora is located in the western Indian Ocean, which probably explains why this genus presents a higher biodiversity in the westernmost part of its area of distribution than in the "Coral Triangle".
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