Spectral fluorometric characterization of Haptophyte dynamics using the FluoroProbe: an application in the eastern English Channel for monitoring Phaeocystis globosa

• Published in: Journal of plankton research Vol. 34; no. 2; pp. 136 - 151
• Main Authors: Houliez, Emilie, Lizon, Fabrice, Thyssen, Melilotus, Artigas, Luis Felipe, Schmitt, Francçois G.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.02.2012; Oxford University Press (OUP)
• Subjects: Animal and plant ecology; Animal, plant and microbial ecology; Biological and medical sciences; Ecology, environment; Fundamental and applied biological sciences. Psychology; General aspects; Isochrysis; Life Sciences; Phaeocystis globosa; Symbiosis; Synecology; English Channel; Atlantic Ocean; North Atlantic; ANE, Europe, English Channel; Haptophytes; chlorophyll; phytoplankton quantification; algal blooms; spectral fluorescence; Characterization; Phaeocystis; Plankton; Dynamics; Haptophyta; Algae
• ISSN: 0142-7873; 1464-3774
• DOI: 10.1093/plankt/fbr091

In this study, we examined the possibility of using the FluoroProbe for monitoring the dynamics of the Haptophyte Phaeocystis globosa in the coastal waters of the eastern English Channel. The FluoroProbe was recalibrated by recording a new fingerprint for P. globosa and the use of this new fingerprint was tested through a series of laboratory and in situ experiments. The annual dynamics of P. globosa estimated using the FluoroProbe and by flow cytometry were similar. A strong relationship was found between the FluoroProbe estimates of P. globosa biomass expressed in terms of chlorophyll a equivalent per litre (eq. µg L−1) and flow cytometric cell counts (r = 0.889, P < 0.001, n = 121). The FluoroProbe can be used to detect the flagellated cells as well as the colonial cells of P. globosa but not to distinguish these two cell types in mixed assemblages. The use of the new fingerprint recorded for P. globosa improved the detection of Isochrysis sp. This suggests the possibility of using the FluoroProbe to monitor Haptophytes other than P. globosa by calibrating the device with species representative of the region of interest. However, it is important to note that the detection of P. globosa at the species level was possible in the eastern English Channel because it was the only Haptophyte species present with a biomass sufficient to be detected by the FluoroProbe. In areas where several Haptophyte species are simultaneously present, their discrimination will be impossible and in such situations the FluoroProbe can be used to monitor the dynamics of the combined Haptophyte group.