2019
DOI: 10.1002/ece3.5533
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Metabolism and foraging strategies of mid‐latitude mesozooplankton during cyanobacterial blooms as revealed by fatty acids, amino acids, and their stable carbon isotopes

Abstract: Increasing sea surface temperatures (SST) and blooms of lipid‐poor, filamentous cyanobacteria can change mesozooplankton metabolism and foraging strategies in marine systems. Lipid shortage and imbalanced diet may challenge the build‐up of energy pools of lipids and proteins, and access to essential fatty acids (FAs) and amino acids (AAs) by copepods. The impact of cyanobacterial blooms on individual energy pools was assessed for key species temperate Temora longicornis and boreal Pseudo‐/Paracalanus spp. that… Show more

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Cited by 15 publications
(10 citation statements)
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“…On the contrary, copepod-dominated zooplankton communities may also facilitate cyanobacteria by praying selectively on the eukaryotic competitors (Ger et al, 2016;Hong et al, 2013). Similar results are found by Eglite et al (2019), who could demonstrate based on fatty acids-, amino acidsand stable carbon isotopes analysis, that mesozooplankton obtained essential fatty acids (FAs) and amino acids (AAs) from cyanobacteria via feeding on mixo-and heterotrophic (dino-)flagellates and detrital complexes. Overall, while copepods play an important grazing role in the ecosystem, they will not be able to control cyanobacteria growth in the Baltic Sea (Sommer et al, 2006).…”
Section: Copepodssupporting
confidence: 65%
“…On the contrary, copepod-dominated zooplankton communities may also facilitate cyanobacteria by praying selectively on the eukaryotic competitors (Ger et al, 2016;Hong et al, 2013). Similar results are found by Eglite et al (2019), who could demonstrate based on fatty acids-, amino acidsand stable carbon isotopes analysis, that mesozooplankton obtained essential fatty acids (FAs) and amino acids (AAs) from cyanobacteria via feeding on mixo-and heterotrophic (dino-)flagellates and detrital complexes. Overall, while copepods play an important grazing role in the ecosystem, they will not be able to control cyanobacteria growth in the Baltic Sea (Sommer et al, 2006).…”
Section: Copepodssupporting
confidence: 65%
“…Arndt proposed that Keratella, through its feeding, enhances leaking of dissolved matter from the algae [ 4 ], thereby supporting the increased biomass of both bacteria and protozoa. Tracer studies suggest that diazotroph nitrogen is mainly incorporated in the Baltic Sea food web by passive leaking of nitrogen compounds by filamentous cyanobacteria [ 64 , 65 ] that stimulate the production of heterotrophic bacteria and picocyanobacteria [ 33 , 34 , 66 ]. Our study confirms that picocyanobacteria are a key resource for the larger zooplankton species, primarily Temora and Centropages, but also, to some extent, Acartia , Bosmina and Synchaeta ( figure 4 a ), and are as such indirectly supported by filamentous cyanobacteria.…”
Section: Discussionmentioning
confidence: 99%
“…Consequently, in the context of library approaches, group differences in FA δ 13 C seem most suitable to complement other methods such as FA source-tracking [60,61] or AA isotope-based library approaches [65]. Nevertheless, FA isotope-based approaches relying on direct source sampling have great potential to assess trophic interactions [13,66,67]. This is reflected by significant differences in standardized FA δ 13 C we found among specific algae species (e.g.…”
Section: (A) Algae Source Separationmentioning
confidence: 96%