Biohydrogen production from food industry waste by suspended and immobilized thermophylic bacteria

This work describes hydrogen production by anaerobic digestion of glucose, molasses and milk whey by 4 thermophilic Thermotoga strains. In the attached-cell tests, the biofilm support characterized by the highest specific surface resulted in the best H2 rate. All the Thermotoga strains examined (T. neapolitana, T. maritima, T. naphtophila, T. petrophila) could produce H2 from glucose, molasses and milk whey, both in suspended- and attached-cell tests. With all the three substrates, the best performances were obtained with T. neapolitana. Some tests were conducted out to select the optimal carrier for the attached-cell conditions. 4 types of carrier were tested: 3 sintered glass carriers and a ceramic one; the chosen carrier was Biomax.

Climate-induced interannual variability of marine primary and export production in three global coupled climate carbon cycle models

Fully coupled climate carbon cycle models are sophisticated tools that are used to predict future climate change and its impact on the land and ocean carbon cycles. These models should be able to adequately represent natural variability, requiring model validation by observations. The present study focuses on the ocean carbon cycle component, in particular the spatial and temporal variability in net primary productivity (PP) and export production (EP) of particulate organic carbon (POC). Results from three coupled climate carbon cycle models (IPSL, MPIM, NCAR) are compared with observation-based estimates derived from satellite measurements of ocean colour and results from inverse modelling (data assimilation). Satellite observations of ocean colour have shown that temporal variability of PP on the global scale is largely dominated by the permanently stratified, low-latitude ocean (Behrenfeld et al., 2006) with stronger stratification (higher sea surface temperature; SST) being associated with negative PP anomalies. Results from all three coupled models confirm the role of the low-latitude, permanently stratified ocean for anomalies in globally integrated PP, but only one model (IPSL) also reproduces the inverse relationship between stratification (SST) and PP. An adequate representation of iron and macronutrient co-limitation of phytoplankton growth in the tropical ocean has shown to be the crucial mechanism determining the capability of the models to reproduce observed interactions between climate and PP.

(Figure 3d) Export production reconstruction based on planktonic foraminiferal sampled in surface sediments

To reconstruct Export Productivity (Pexp), 27 taxonomic categories of the planktonic foraminifera census data were used with the modern analog technique SIMMAX 28 (Pflaumann et al., 1996, doi:10.1029/95PA01743; 2003, doi:10.1029/2002PA000774). To the 26 taxonomic groups widely used and listed in Kucera et al. (2005, doi:10.1016/j.quascirev.2004.07.014), Turborotalita humilis was added in our calibration as it is associated with the PCC source region (Meggers et al., 2002, doi:10.1016/S0967-0645(02)00103-0). The modern analog file is based on the Iberian margin database (Salgueiro et al., 2008, doi:10.1016/j.marmicro.2007.09.003) combined with the North Atlantic surface samples used by the MARGO project (Kucera et al., 2005). This results in a total of 999 analogs for Pexp. Modern oceanic primary productivity (PP) is obtained for each site by averaging 12 monthly primary productivity values for a 8-year period (1978-1986) that were estimated from satellite color data (CZCS) and gridded at 0.5° latitude - longitude fields (Antoine et al., 1996, doi:10.1029/95GB02832). Export Productivity (Pexp) was calculated from the PP values following the empirical relationship Pexp = PP**2/400 for primary production below 200 gC/m**2/yr, and Pexp = PP/2 for primary production above 200 gC/m2/yr (Eppley and Peterson, 1979, doi:10.1038/282677a0; Sarnthein et al., 1988, doi:10.1029/PA003i003p00361). The residuals gives the differences between satellite based Pexp and foraminiferal Pexp.