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The global distribution of chromophoric dissolved organic matter (CDOM) in the euphotic layer of the Atlantic, Indian and Pacific oceans (between 35º N and 40º S) was analysed by absorption spectroscopy during the Malaspina 2010 circumnavigation. Absorption coefficients at 254 nm (a254) and 325 nm (a325), indices (a254/a365) and spectral slopes (between 275-295 nm, S275-295) were calculated from the dissolved fraction of the UV absorption spectra to describe the amount and quality of CDOM. Generalized additive models (GAMs) were applied to evaluate the relevance of physical and biogeochemical drivers of the variability of CDOM. Besides the low CDOM values, a first division of our data following the Longhurst's biogeographic classification showed significant differences in CDOM levels among provinces. The lowest values of a254 and a325 were found in the oligotrophic gyres, particularly in the Indian Ocean, and the highest in the upwelling areas, particularly in the Equatorial Pacific. Opposite distributions were obtained for S275-295 and a254/a365, indicative of higher photobleaching in the gyres. Within each province, whereas a254 was constant through the photic layer, a325 increased significantly with depth as a result of the dominance of photobleaching over biological production in the surface layer and the opposite at depth. The Pacific provinces, including the subtropical gyres, showed however significantly higher a325 values, indicative of lower photobleaching/higher biological production. The GAM analysis indicates that a254 and a325 were primarily related to chlorophyll a, exhibiting a significant positive linear response. Apparent oxygen utilization also contributed to explain the distributions of these absorption coefficients, being inversely related to a254 and directly related to a325. These results are consistent with the premise that a254 could be a proxy for the concentration of dissolved organic carbon and a325 for the aromatic by-products of biological degradation. The GAM analysis also shows that a254/a365 and S275-295 exhibited inverse relationships with solar radiation, indicating that the biological production of CDOM counteracts photodegradation as solar radiation increases. In summary, whereas photobleaching dictates the vertical distribution of CDOM, chlorophyll a explains the CDOM differences among the photic layer of the tropical and subtropical ocean provinces visited during the circumnavigation.
The observation that the relative importance of picophytoplankton is greatest in warm and nutrient‐poor waters was tested here based on a comprehensive review of the data available in the literature from oceanic and coastal estuarine areas. Results show that picophytoplankton dominate (≥50%) the biomass and production in oligotrophic (chlorophyll a [Chl a ] < 0.3 mg m −3 ), nutrient poor (NO 3 + NO 2 < 1 µM), and warm (>26°C) waters, but represent <10% of autotrophic biomass and production in rich (Chl a > 5 mg m −3 ) and cold <3°C) waters. There is, however, a strong covariation between temperature and nutrient concentration ( r = −0.95, P < 0.001), but the number of observations where both temperature and nutrient concentrations are available is too small to allow attempts to statistically separate their effects. The results of mesocosm nutrient addition experiments during summer in the Mediterranean Sea allowed the dissociation of the effects of temperature from those of nutrients on pico phytoplankton production and biomass and validated the magnitude at which picoplankton dominates (≥50%) autotrophic biomass and production obtained in the comparative analysis. The fraction contributed by picoplankton significantly declined ( r 2 = 0.76 and 0.90, respectively, P < 0.001) as total autotrophic production and biomass increased. These results support the increasing importance of picophytoplankton in warm, oligotrophic waters. The reduced contribution of picophytoplankton in warm productive waters is hypothesized here to be due to increased loss rates, whereas the dominance of picophytoplankton in warm, oligotrophic waters is attributable to the differential capacity to use nutrients as a function of differences in size and capacity of intrinsic growth of picophytoplankton and larger phytoplankton cells.
Abstract Coral reefs are under rapid decline due to human pressures such as climate change. Achieving the Kunming-Montreal Global Biodiversity Framework goals, which include restoring 30% of degraded habitats like coral reefs by 2030, requires a comprehensive understanding of their extent and structure, which has been hitherto lacking. We address this limitation based on the unprecedented canonical inventory of coral reefs extracted from the Allen Coral Atlas of shallow-water tropical reefs. We identified a total of 1,579,772 individual reefs globally, extending over a total of 52,423 km 2 of ocean area with mean and median sizes of 3.32 ha and 0.3 ha, respectively. We unravelled three universal laws that are common to all coral reef provinces: the size-frequency distribution, the inter-reef distance distribution and the area-perimeter relation, which follow power laws with an exponent of 1.8, 2.33 and 1.26, respectively. We demonstrate that coral reefs develop universal fractal patterns characterised by a perimeter fractal dimension of D P = 1.3 and a surface fractal dimension of D A = 1.6. Our analysis shows that coral reefs display intricate fractal-like geometries and exhibit universal macroecological patterns, largely independent of their geographical location. The universality of the observed patterns suggests that these features possibly stem from the highly conserved interactions of biological, physical, and chemical processes. Over geological scales, these processes lead to reef landscape patterns common among all provinces, providing new information relevant to reef growth modelling.
MEPS Marine Ecology Progress Series Contact the journal Facebook Twitter RSS Mailing List Subscribe to our mailing list via Mailchimp HomeLatest VolumeAbout the JournalEditorsTheme Sections MEPS 137:203-213 (1996) - doi:10.3354/meps137203 Growth and population dynamics of Posidonia oceanica on the Spanish Mediterranean coast: elucidating seagrass decline Marbà N, Duarte CM, Cebrián J, Gallegos ME, Olesen B, Sand-Jensen K The growth and population dynamics of Posidoniaoceanica were examined in 29 meadows along 1000 km of the Spanish Mediterranean coast (from 36*46' to 42*22'N). P.oceanica developed the densest meadows (1141 shoots m-2) and the highest aboveground biomass (1400 g DW m-2) between 38 and 39*N. P.oceanica shoots produced, on average, 1 leaf every 47 d, though leaf formation rates in the populations increased from north to south (range 5.7 to 8.9 leaves shoot-1 yr-1). P.oceanica is a long-living seagrass, with shoots able to live for at least 30 yr. P.oceanica recruited shoots at low rates (0.02 to 0.5 ln units yr-1) which did not balance the mortality rates (0.06 to 0.5 ln units yr-1) found in most (57%) of the meadows. If the present disturbance and rate of decline are maintained, shoot density is predicted to decline by 50% over the coming 2 to 24 yr. Because P.oceanica rhizomes grow very slowly (1 to 6 cm yr-1 apex-1), maintenance of existing meadows is essential, and our results suggest bad future prospects for P.oceanica in the Spanish Mediterranean Sea like most other seagrass species in the world oceans. Leaf growth . Rhizome growth . Shoot demography . Posidonia oceanica . Seagrass decline Full text in pdf format PreviousNextExport citation RSS - Facebook - Tweet - linkedIn Cited by Published in MEPS Vol. 137. Publication date: June 27, 1996 Print ISSN:0171-8630; Online ISSN:1616-1599 Copyright © 1996 Inter-Research.
Abstract. The Arctic Ocean is considered the most vulnerable ecosystem to ocean acidification (OA) and large-scale assessments of pH and the saturation state for aragonite (Ωarag) indicate that it is already close to corrosive states (Ωarag < 1). In high-latitude coastal waters the regulation of pH and Ωarag is far more complex than offshore because increased biological activity and input of glacial meltwater affect pH. As most calcifiers occupy coastal habitats, the assessment of risks from OA to these vulnerable organisms cannot be derived from extrapolation of current and forecasted offshore conditions, but requires an understanding of the regimes of pH and Ωarag in their coastal habitats. To increase knowledge of the natural variability of pH in the Arctic coastal zone and specifically to test the influence of benthic vegetated habitats, we quantified pH-variability in a Greenland fjord in a nested scale approach. A sensor array logging pH, O2, PAR, temperature and salinity was applied on spatial scales ranging from km-scale across the horizontal extension of the fjord, over 100 m scale vertically in the fjord, 10–100 m scale between subtidal habitats with and without kelp forests and between vegetated tidal pools and adjacent vegetated shores, to cm-m scale within kelp forests and mm-scale across boundary layers of macrophyte tissue. In addition, we assessed the temporal variability in pH on diurnal and seasonal scales. Based on pH-measurements combined with relationships between salinity, total alkalinity and dissolved inorganic carbon we also estimated variability of Ωarag. Results show variability in pH and Ωarag of up to 0.2–0.3 units at several scales, i.e. along the horizontal and vertical extension of the fjord, between seasons and on a diel basis in benthic habitats and within 1 m3 of kelp forest. Vegetated intertidal pools exhibited extreme diel pH variability of > 1.5 units and macrophyte boundary layers a pH-range of up to 0.8 units. Overall, Ωarag was favorable to calcification, and pelagic and benthic metabolism was an important driver of pH and Ωarag producing mosaics of variability from low levels in the dark to peak levels at high irradiance. We suggest that productive coastal environments may form niches of high pH in a future acidified Arctic Ocean.