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Since the 1990s red-tide blooms of Fibrocapsa japonica have frequently been observed in European waters; despite their recurrence also in the Adriatic coastal areas, they have never been conclusively linked to ichthyotoxic events. Since the toxicity of F. japonica is still under debate and its effects differ among the strains, in this study all the compounds previously postulated as involved in the toxic mechanism, such as brevetoxins, fatty acids and ROS, were screened for Adriatic strains. Whole algal extracts were analyzed for brevetoxin PbTx-2, which was not found, and for a qualitative and quantitative analysis of fatty acids. The fatty acid profile evidenced the presence of PUFAs, with considerable amounts of 18:4n-3, 20:4n-6, and 20:5n-3, as already found in different strains, but with a lower amount of arachidonic acid (20:4n-6). None of the PUFAs was released in the extracellular medium. Different toxicological assays (Vibrio fischeri, Artemia sp., haemolysis of fish erythrocytes) were performed using algal cellular, extracellular or subcellular samples as well as fractions of the algal extract, in order to identify the toxic compounds. The tested cultures were found to inhibit V. fischeri bioluminescence, to affect Artemia nauplii viability and to have haemolytic effects comparable to those previously observed in different strains. The solid phase extraction (SPE) of the Adriatic F. japonica extracts resulted in a high concentration of PUFAs in two main fractions, which caused mortality in Artemia nauplii and inhibition of V. fischeri bioluminescence. Fish (Dicentrarchus labrax) assays were also performed, reporting mortality after long exposure times and the cause of fish death was investigated. A significant increase of H2O2 in the tanks where sea basses were exposed to F. japonica was obtained, indicating that the presence of fish stimulates H2O2 production by algal cells and leading to the hypothesis of H2O2 involvement in F. japonica toxicity. The presence of oxidative stress in the exposed fish was confirmed by the increased malondialdehyde concentration in their gills. Overall these results indicate that since F. japonica cells can easily cling to fish gills, due to their high polysaccharide production, it is presumable that high PUFA amounts are released in loco, as a result of cell breakage, and that exert their toxicity together with ROS. This study shows that the Adriatic strains of F. japonica can be harmful to higher level organisms. Nevertheless a high cell density and a long lasting bloom are necessary to cause severe damage to fish gills or death for crustaceans.

The spatial and temporal distribution of the toxic benthic dinoflagellate Ostreopsis ovata was investigated along the Conero Riviera (northern Adriatic Sea) during summer 2007 to evaluate the role of substratum, depth and hydrodynamic conditions on bloom dynamics. Sampling was carried out from April to November on different substrata (seaweeds, mollusc shells and rocks) and in the water column. O. ovata bloom started in September, reaching maximum values in the first week of October (1.7 × 106 cells g−1 fw corresponding to 21.0 × 106 cells g−1 dw and 6.2 × 104 cells cm−2) and completely disappearing at the beginning of November. On average, the abundances of O. ovata on rocks were significantly higher than those on seaweeds. Seaweeds with branched thalli supported higher values of epiphytes than non-branched ones. The abundances of O. ovata were significantly higher in sheltered than in exposed sites indicating a major role of hydrodynamism in regulating bloom dynamics. O. ovata abundances showed a marked decrease with depth with significantly lower values at depths >3 m. In the northern Adriatic, bloom development did not show any relationship with temperature, as the peak occurred when temperature values were decreasing.

The effects of temperature, salinity, inorganic and organic nutrients on the growth and physiological performance of Fibrocapsa japonica have been investigated in strains isolated from the northern Adriatic Sea, where intense and regular blooms have occurred since 1997 in coastal waters during summer. Strains isolated at different times and from different locations appeared homogeneous in terms of both physiological responses and molecular (ITS-5.8S rDNA) characteristics. Growth rates were higher at temperatures between 20 and 26 °C and in a salinity range of 30–35 (0.7 div day −1 ). The temperature of 16 °C inhibited growth, more markedly at the lowest and highest salinity values, a result also confirmed by a lower photosynthetic efficiency and by an increase in cell volume due to impaired division. Higher cell concentrations were obtained with macronutrients at f/2 levels than in a fivefold diluted medium. Comparing the utilization of 200 μM nitrate to that of different N sources (inorganic and organic), F. japonica showed an efficient growth with equivalent amounts of ammonia, urea and amino acids, such as glycine and tryptophan; glutamate was less effective, while methionine had toxic effects. Organic phosphate, administered as glycerophosphate, could also sustain F. japonica growth, probably on account of an alkaline phosphatase whose activity was enhanced in the presence of the organic form. Vitamins were necessary for growth, though no further stimulation was observed when a surplus of vitamin B12 (3 nM) was added. The addition of 11.7 μM iron instead of 2.3 μM, as well as that of humic acid, with or without macronutrients, did not enhance algal growth either. These results led us to hypothesise that F. japonica blooms became more frequent due to a general seawater temperature increase and to the availability of organic forms which, in coastal anthropized areas, are especially abundant in summer periods.

Fibrocapsa japonica resting cysts were detected in coastal sediments of the Marche region (northern Adriatic Sea, Italy), where summer blooms regularly occur. Sampling was carried out along 18 transects (2 stations each) during May–June 2007. The identification and counting of raphidophyte cysts were carried out under the inverted microscope and molecular analyses were applied to sediment samples to confirm species-specific identification. Raphidophyte cysts were recorded in almost all stations with maximum abundance of 9 ± 5 and 12 ± 3 cysts g−1 dw for cysts of F. japonica and undetermined Raphidophyceae, respectively. Cyst formation was induced in F. japonica monoclonal cultures under different conditions: shadow-optimal temperature and dark-low temperature treatment; both experiments were performed at two salinity values (30 and 35). Cyst formation (preliminary cysts) was observed in both experiments, although with different encystment rates. However, only a further permanence in the dark at 15 °C in microplates led to the formation of mature cysts, probably supported by the possibility to adhere to solid surfaces. Before pre-cyst formation, vegetative cells showed a cytoplasmatic “brown body”.