In this paper, the production of the microalga Nannochloropsis gaditana using centrate from the anaerobic digestion of treated urban wastewater is studied. For this, semicontinuous cultures were performed indoors at laboratory scale, under controlled conditions, supplying seawater with different centrate percentages from a real wastewater treatment plant as the culture medium. It was demonstrated that N. gaditana can be produced using solely centrate as the nutrient source but only at percentages below 50%. Above this level, inhibition is caused by an excess of ammonia, thus reducing productivity. In the 30-50% centrate range, biomass productivity was 0.4 g·l −1 ·day −1 , equal to that measured when using Algal culture medium. Moreover, the biochemical composition of the biomass was also equal to that measured when using Algal culture medium, with the protein content in the 30-40% d.wt. range; whereas the lipid content ranged from 20 to 25% d.wt. Under these conditions, phosphorus depuration from the culture medium was in the 80-90% range while nitrogen depuration was only between 20 and 40%, indicating an excess of nitrogen in the centrate with respect to phosphorus. In spite of this phosphorus limitation, in the optimal centrate range (30-50% in the culture medium), the cells performed under optimal conditions, removing up to 35 mg N ·l −1 ·day −1 and 5.7 mg P ·l −1 ·day −1 , with quantum yield values measuring 1.0-1.3 g·E −1 . By supplying additional phosphorus, it was possible to enhance productivity and increase nitrate and phosphorus depuration to over 80%. The use of centrate is confirmed as a useful method for reducing microalgae production costs while also increasing process sustainability, especially when using biomass for bioenergy applications.

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Entomopathogenic nematodes are a subgroup of insect-parasitic nematodes that are used in biological control as alternatives or supplements to chemical pesticides. Steinernema scapterisci is an unusual member of the entomopathogenic nematode guild for many reasons including that it is promiscuous in its association with bacteria, it can reproduce in the absence of its described bacterial symbiont, and it is known to have a narrow host range. It is a powerful comparative model within the species and could be used to elucidate parasite specialization. Here we describe a new method of efficiently producing large numbers of S. scapterisci infective juveniles (IJs) in house crickets and for quantifying parasitic activation of the IJs upon exposure to host tissue using morphological features. We found that parasite activation is a temporal process with more IJs activating over time. Furthermore, we found that activated IJs secrete a complex mixture of proteins and that S. scapterisci IJs preferentially activate upon exposure to cricket tissue, reaffirming the description of S. scapterisci as a cricket specialist.

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