The use of satellites to monitor the color of the ocean requires effective removal of the atmospheric signal. This can be performed by extrapolating the aerosol optical properties in the visible from the near-infrared (NIR) spectral region assuming that the seawater is totally absorbant in this latter part of the spectrum. However, the non-negligible water-leaving radiance in the NIR which is characteristic of turbid waters may lead to an overestimate of the atmospheric radiance in the whole visible spectrum with increasing severity at shorter wavelengths. This may result in significant errors, if not complete failure, of various algorithms for the retrieval of chlorophyll-a concentration, inherent optical properties and biogeochemical parameters of surface waters. This paper presents results of an inter-comparison study of three methods that compensate for NIR water-leaving radiances and that are based on very different hypothesis: 1) the standard Sea WiFS algorithm (Stumpfet al., 2003; Bailey et al., 2010) based on a bio-optical model and an iterative process; 2) the algorithm developed by Ruddick et al. (2000) based on the spatial homogeneity of the NIR ratios of the aerosol and water-leaving radiances; and 3) the algorithm of Kuchinke et al. (2009) based on a fully coupled atmosphere-ocean spectral optimization inversion. They are compared using normalized water-leaving radiance nL(w) in the visible. The reference source for comparison is ground-based measurements from three AERONET-Ocean Color sites, one in the Adriatic Sea and two in the East Coast of USA. Based on the matchup exercise, the best overall estimates of the nL(w) are obtained with the latest SeaWiFS standard algorithm version with relative error varying from 14.97\% to 35.27\% for lambda = 490 nm and lambda = 670 nm respectively. The least accurate estimates are given by the algorithm of Ruddick, the relative errors being between 16.36\% and 42.92\% for lambda = 490 nm and lambda = 412 nm, respectively. The algorithm of Kuchinke appears to be the most accurate algorithm at 412 nm (30.02\%), 510 (15.54\%) and 670 nm (32.32\%) using its default optimization and bio-optical model coefficient settings. Similar conclusions are obtained for the aerosol optical properties (aerosol optical thickness tau(865) and the Angstrom exponent, alpha(510, 865)). Those parameters are retrieved more accurately with the SeaWiFS standard algorithm (relative error of 33\% and 54.15\% for tau(865) and alpha(510, 865)). A detailed analysis of the hypotheses of the methods is given for explaining the differences between the algorithms. The determination of the aerosol parameters is critical for the algorithm of Ruddick et al. (2000) while the bio-optical model is critical for the algorithm of Stumpf et al. (2003) utilized in the standard SeaWiFS atmospheric correction and both aerosol and bio-optical model for the coupled atmospheric-ocean algorithm of Kuchinke. The Kuchinke algorithm presents model aerosol-size distributions that differ from real aerosol-size distribution pertaining to the measurements. In conclusion, the results show that for the given atmospheric and oceanic conditions of this study, the SeaWiFS atmospheric correction algorithm is most appropriate for estimating the marine and aerosol parameters in the given turbid waters regions. (C) 2011 Elsevier Inc. All rights reserved.
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P1. Positive effects of species diversity on ecosystem functioning have often been demonstrated in 'macrobial' communities. This relation and the responsible mechanisms are far less clear for microbial communities. Most experimental studies on microorganisms have used randomly assembled communities that do not resemble natural communities. It is therefore difficult to predict the consequences of realistic, non-random diversity loss. 2. In this study, we used naturally co-occurring diatom species from intertidal mudflats to assemble communities with realistically decreasing diversity and analysed the effect of non-random species loss on biomass production. 3. Our results demonstrate a highly positive biodiversity effect on production, with mixtures outperforming the most productive component species in more than half of the combinations. These strong positive diversity effects could largely be attributed to positive complementarity effects (including both niche complementarity and facilitation), despite the occurrence of negative selection effects which partly counteracted the positive complementarity effects at higher diversities. 4. Facilitative interactions were, at least in part, responsible for the higher biomass production. For one of the species, Cylindrotheca closterium, we show its ability to significantly increase its biomass production in response to substances leaked into the culture medium by other diatom species. In these conditions, the species drastically reduced its pigment concentration, which is typical for mixotrophic growth. 5. Synthesis. We show that both species richness and identity have strong effects on the biomass production of benthic diatom biofilms and that transgressive overyielding is common in these communities. In addition, we show mechanistic evidence for facilitation which is partly responsible for enhanced production. Understanding the mechanisms by which diversity enhances the performance of ecosystems is crucial for predicting the consequences of species loss for ecosystem functioning.
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