12 pages, 6 figures, 6 tablesA life cycle assessment (LCA) and an energy balance analysis of marine microalgal biomass production were conducted to determine the environmental impacts and the critical points of production for large scale planning. The artificial lighting and temperature conditions of an indoor bubble column photobioreactor (bcPBR) were compared to the natural conditions of an equivalent outdoor system. Marine microalgae, belonging to the dinoflagellate and raphidophyte groups, were cultured and the results were compared with published LCA data obtained from green microalgae (commonly freshwater algae). Among the species tested, Alexandrium minutum was chosen as the target marine microalgae for biomass production under outdoor conditions, although there were no substantial differences between any of the marine microalgae studied. Under indoor culture conditions, the total energy input for A. minutum was 923 MJ kg−1 vs. 139 MJ kg−1 for outdoor conditions. Therefore, a greater than 85% reduction in energy requirements was achieved using natural environmental conditions, demonstrating the feasibility of outdoor culture as an alternative method of bioenergy production from marine microalgae. The growth stage was identified as the principal source of energy consumption for all microalgae tested, due to the electricity requirements of the equipment, followed by the construction material of the bcPBR. The global warming category (GWP) was 6 times lower in outdoor than in indoor conditions. Although the energy balance was negative under both conditions, this study concludes with suggestions for improvements in the outdoor system that would allow up-scaling of this biomass production technology for outdoor conditions in the MediterraneanThe authors would like to thank to Comisión Nacional de Investigación Ciencia y Tecnología (CONICYT) from Chile for supporting the scholarship “Beca de Gestión Propia,” which finances the PhD studies of C. Fuentes-Grünewald; and to Spanish Ministry of Science and Innovation for supporting the work of E. Garcés and S. Rossi by the Ramon and Cajal award. The authors would like also to thank S. Fraga for providing the clonal culture AMP4, Laura del Río and Xavi Leal for their help with the experiments, and the Zona Acuarios Experimentales (ZAE) of the ICM-CSIC for the use of their facilities. The authors would like also to thank to project Ecotech SudoeSOE2/P2/E377 for its financial support.Peer reviewe

Parasitoids are a major top-down cause of mortality of coastal harmful algae, but the mechanisms and strategies they have evolved to efficiently infect ephemeral blooms are largely unknown. Here, we show that the generalist dinoflagellate parasitoid Parvilucifera sinerae (Perkinsozoa, Alveolata) is activated from dormancy, not only by Alexandrium minutum cells but also by culture filtrates. We unequivocally identified the algal metabolite dimethylsulphide (DMS) as the density-dependent cue of the presence of potential host. This allows the parasitoid to alternate between a sporangium-hosted dormant stage and a chemically-activated, free-living virulent stage. DMS-rich exudates of resistant dinoflagellates also induced parasitoid activation, which we interpret as an example of coevolutionary arms race between parasitoid and host. These results further expand the involvement of dimethylated sulphur compounds in marine chemical ecology, where they have been described as foraging cues and chemoattractants for mammals, turtles, birds, fish, invertebrates and plankton microbes.

Two different strains of microalgae, one raphidophyte and one dinoflagellate, were tested under different abiotic conditions with the goal of enhancing lipid production. Whereas aeration was crucial for biomass production, nitrogen deficiency and temperature were found to be the main abiotic parameters inducing the high-level cellular accumulation of neutral lipids. Net neutral lipid production and especially triacylglycerol (TAG) per cell were higher in microalgae (>200% in Alexandrium minutum, and 30% in Heterosigma akashiwo) under treatment conditions (25°C; 330 μM NaNO₃) than under control conditions (20°C; 880 μM NaNO₃). For both algal species, oil production (free fatty acids plus TAG fraction) was also higher under treatment conditions (57 mg L⁻¹ in A. minutum and 323 mg L⁻¹ in H. akashiwo). Despite the increased production and accumulation of lipids in microalgae, the different conditions did not significantly change the fatty acids profiles of the species analyzed. These profiles consisted of saturated fatty acids (SAFA) and polyunsaturated fatty acids (PUFA) in significant proportions. However, during the stationary phase, the concentrations per cell of some PUFAs, especially arachidonic acid (C20:4n6), were higher in treated than in control algae. These results suggest that the adjustment of abiotic parameters is a suitable and one of the cheapest alternatives to obtain sufficient quantities of microalgal biomass, with high oil content and minimal changes in the fatty acid profile of the strains under consideration.