Allelochemicals determine competition and grazing control in Alexandrium catenella.

Alexandrium catenella Allelochemicals Food web model Grazing experiment Harmful dinoflagellate Microzooplankton Paralytic Shellfish Toxins (PSTs)

Journal

Harmful algae
ISSN: 1878-1470
Titre abrégé: Harmful Algae
Pays: Netherlands
ID NLM: 101128968

Informations de publication

Date de publication:
Sep 2024
Historique:
received: 06 11 2023
revised: 15 05 2024
accepted: 31 07 2024
medline: 8 9 2024
pubmed: 8 9 2024
entrez: 7 9 2024
Statut: ppublish

Résumé

The production of allelochemicals by the toxigenic dinoflagellate Alexandrium catenella is one of the suggested mechanisms to facilitate its bloom formation and persistence by outcompeting other phototrophic protists and reducing grazing pressure. In Southern California, toxic events caused by A. catenella and paralytic shellfish toxins (PSTs) regularly impact coastal ecosystems; however, the trophic interactions and mechanisms promoting this species in a food web context are still not fully understood. In the present study, we combined a dynamical mathematical model with laboratory experiments to investigate potential toxic and allelochemical effects of an A. catenella strain isolated off the coast of Los Angeles, Southern California, on competitors and a common zooplankton consumer. Experiments were conducted using three toxigenic strains of A. catenella, comparing the new Californian isolate (Alex Cal) to two strains previously described from the North Sea, a lytic (Alex2) and non-lytic (Alex5) strain, testing for donor density-dependent effects on two phytoplankton species (Rhodomonas salina, Tetraselmis sp.) and on the rotifer Brachionus plicatilis. Bioassays revealed a steep decline in competitor and consumer populations with increasing Alex Cal concentrations, indicating an intermediate lytic activity compared to the North Sea strains (lytic Alex2 and non-lytic Alex5). The rotifer fed and grew well on the PST- toxic, but non-lytic Alex5 strain, while its survival significantly decreased with increasing concentrations of the two lytic strains Alex Cal and Alex 2, indicating that negative effects on the rotifer were mediated by allelochemicals rather than PST-toxins. Mixed culture experiments including both competitors and consumers demonstrated that the intensity of allelochemical effects not only depended on the A. catenella density but also on the target density. Negative effects on grazers were alleviated by co-occurring competitors with a lower sensitivity to allelochemicals, thus reducing harmful compounds and allowing grazing control on the dinoflagellate to come into effect again. Results from mixed culture experiments were supported by the mathematical approach used in this study which was calibrated with data from simple monoculture growth, pairwise competition and predator-prey experiments, demonstrating the applicability of this model approach to predict the outcome of more complex food web dynamics at the community level.

Identifiants

pubmed: 39244239
pii: S1568-9883(24)00137-9
doi: 10.1016/j.hal.2024.102704
pii:
doi:

Substances chimiques

Pheromones 0
Marine Toxins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102704

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest I hereby declare on behalf of all authors that we have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Stefanie D Moorthi (SD)

Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky Universität Oldenburg, School of Mathematics and Science, Ammerländer Heerstraße 114-118, 26219 Oldenburg, Germany. Electronic address: stefanie.moorthi@uni-oldenburg.de.

Michaela Busch (M)

Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky Universität Oldenburg, School of Mathematics and Science, Ammerländer Heerstraße 114-118, 26219 Oldenburg, Germany.

Ulrike Feudel (U)

Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky Universität Oldenburg, School of Mathematics and Science, Ammerländer Heerstraße 114-118, 26219 Oldenburg, Germany.

Urban Tillmann (U)

Vrije Universiteit Amsterdam, Faculty of Science, de Boelelaan 1085, 1081 HV Amsterdam, the Netherlands.

Bernd Krock (B)

Alfred-Wegener-Institute for Polar and Marine Research, Am Handelshafen 12, 27570 Bremerhaven, Germany.

Bob W Kooi (BW)

Vrije Universiteit Amsterdam, Faculty of Science, de Boelelaan 1085, 1081 HV Amsterdam, the Netherlands.

Jana Brinkmann (J)

Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky Universität Oldenburg, School of Mathematics and Science, Ammerländer Heerstraße 114-118, 26219 Oldenburg, Germany.

Subhendu Chakraborty (S)

Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky Universität Oldenburg, School of Mathematics and Science, Ammerländer Heerstraße 114-118, 26219 Oldenburg, Germany; Systems Ecology Group, Leibniz Centre for Tropical Marine Research (ZMT), 28359 Bremen, Germany.

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Classifications MeSH