Marine microalgae are considered a potentially new and valuable source of biologically active molecules for applications in the food industry as well as in the pharmaceutical, nutraceutical, and cosmetic sectors. They can be easily cultured, have short generation times and enable an environmentally-friendly approach to drug discovery by overcoming problems associated with the over-utilization of marine resources and the use of destructive collection practices. In this study, 21 diatoms, 7 dinoflagellates, and 4 flagellate species were grown in three different culturing conditions and the corresponding extracts were tested for possible antioxidant, anti-inflammatory, anticancer, anti-diabetes, antibacterial, and anti-biofilm activities. In addition, for three diatoms we also tested two different clones to disclose diversity in clone bioactivity. Six diatom species displayed specific anti-inflammatory, anticancer (blocking human melanoma cell proliferation), and anti-biofilm (against the bacteria Staphylococcus epidermidis) activities whereas, none of the other microalgae were bioactive against the conditions tested for. Furthermore, none of the 6 diatom species tested were toxic on normal human cells. Culturing conditions (i.e., nutrient starvation conditions) greatly influenced bioactivity of the majority of the clones/species tested. This study denotes the potential of diatoms as sources of promising bioactives for the treatment of human pathologies.

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), a high frequency of dead cells (up to 15%) and cells with starch granules (up to 93%), and no evidence of recent mixotrophic behaviour. Still, the cells, which did not perform vertical migration, aggregated around salinity-driven density discontinuities in the top 5 m and had a high cell toxin quota (determined by liquid chromatography-mass spectrometry) for this species. A 3.5-fold difference was found between maximum (during the night) and minimum values of cell toxin quota. Okadaic acid (OA) was the predominant toxin and changes in cell quota of different toxins showed different daily patterns in the content of okadaiates and pectenotoxins; thus, the toxin profile is influenced by the time of sampling. Dissolved toxins (adsorbed by resins in passive samplers from 8 to 14 November) also reached annual maxima and reflected the vertical distribution of D. acuta cells. These results emphasize the need to parameterize physiological conditions and behaviour of Dinophysis populations during different phases of the population growth and hydrodynamic scenarios.