Effect of heterotrophic versus autotrophic food on feeding and reproduction of the calanoid copepod Acartia tonsa : relationship with prey fatty acid composition
By E. Broglio, S. Jónasdóttir, A. Calbet, H. Jakobsen, E. Saiz. 2003
177 citations recorded by the source corpus.
Subfields: Ecology, Global and Planetary Change, Oceanography
View Paper: https://www.semanticscholar.org/paper/a87a3d1bdf7e21f8e9a960ad46b31ab59baa473a
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In Ecology
In Global and Planetary Change
In Oceanography
- A. Calbet
- E. Saiz
- Aditee Mitra
- M. Boersma
- Kevin J. Flynn
- Kwok-Fung Tang
- Thomas R. Anderson
- C. Meunier
Citations in the corpus
- The role of ciliates, heterotrophic dinoflagellates and copepods in structuring spring plankton communities at Helgoland Roads, North Sea (2011, background): “Filling and mixing procedures during experiments (Gifford 1985; Landry 1993; Broglio et al. 2003) can cause considerable losses, and a high mortality of, e.g., ciliates had been reported previously (up to 80%, Tiselius 1989).”
- Protozoans as a food source for Antarctic krill, Euphausia superba: Complementary insights from stomach content, fatty acids, and stable isotopes (2006, background): “The basic assumption is that 18:1(n-7) represents feeding on phytoplankton, while metazoan and some protozoans contain more 18:1(n-9) (Falk-Petersen et al. 2000; Broglio et al. 2003).”
- The ciliate-copepod link in marine ecosystems (2005, background): “Moreover, ciliates can also be employed as direct sources of proteins, amino acids, and important polyunsaturated fatty acids (PUFA), for the reproduction of crustaceans (Stoecker & Capuzzo 1990, Wickham 1995, Broglio et al. 2003).”
- Trophic modification of essential fatty acids by heterotrophic protists and its effects on the fatty acid composition of the copepod Acartia tonsa (2006, background): “Both EPA and DHA were detected in the two protozoans when they fed on D. tertiolecta.”
- Bridging the gap between marine biogeochemical and fisheries sciences; configuring the zooplankton link (2014, background): “Additionally, based on stoichiometric and biochemical grounds, microzooplankton, rather than phytoplankton, could be expected to be better prey for mesozooplankton (Klein Breteler et al., 1999; Broglio et al., 2003; Mitra and Flynn, 2005).”
- Lipid biomarkers and trophic linkages between phytoplankton, zooplankton and anchovy (Engraulis encrasicolus) larvae in the NW Mediterranean (2006, unknown): “The accumulate MUFA and PUFA in the zooplankton (Table IV) suggests a ‘storage’ strategy in these organisms (Pond et al., 2000; Hagen et al., 2001).”
- Effects of dietary fatty acids on the reproductive success of the calanoid copepod Temora longicornis (2005, background): “Diatoms could make up the main part of the ingested food, because the diatom biomarker and faecal pellet production both had high scores in the same PCA (Table 7). On the other hand, the coupling between the diatom biomarker and faecal pellet production could alternatively be explained by large amou”
- Trophic impact and prey selection by crustacean zooplankton on the microbial communities of an oligotrophic coastal area (NW Mediterranean Sea) (2004, background): “As mentioned above, consuming ciliates might signify a higher intake of nutritious organic matter than that obtained by consuming algae (excluding, perhaps, autotrophic dinoflagellates; Broglio et al. 2003).”
- Trophodynamics and seasonal cycle of the copepod Pseudocalanus acuspes in the Central Baltic Sea (Bornholm Basin): evidence from lipid composition (2006, background): “Lipid proWles of ciliates have been reported to reXect, at least within speciesspeciWc ranges, the fatty acid composition of their diet (Ederington et al. 1995; Harvey et al. 1997; Broglio et al. 2003 ).”
- Application of liposome and stable isotope tracer techniques to study polyunsaturated fatty acid biosynthesis in marine zooplankton (2007, background): “…by different microplanktonic groups in the marine environment and the availability of these compounds in the diet of marine copepods has been linked to growth rates and reproductive success (Jónasdóttir, 1994; Pond et al., 1996; Kleppel et al. 1999; Broglio et al., 2003; Pond et al., 2005).”
- The effects of temperature and salinity on egg production and hatching success of Baltic Acartia tonsa (Copepoda: Calanoida): a laboratory investigation (2006, background): “Peck and L. Holste, submitted; this study), female age (e.g., Parrish and Wilson 1978) and food concentration and quality (e.g., Kiorboe et al. 1985; Broglio et al. 2003 ).”
- FlowCAM: Sizing cells and understanding the impact of size distributions on biovolume of planktonic community structure (2011, background): “Similarly, species-specific loss between 0 to 40% of ciliates and phytoplankton cells has been observed after addition of Lugol’s solution (Montagnes et al. 1994, Broglio et al. 2003, 2004).”
- Synchronous ecological regime shifts in the central Baltic and the North Sea in the late 1980s (2005, background): “Unlike diatoms, dinoflagellates and heterotrophic protists seem to favour copepod production (Kleppel, 1993; Broglio et al., 2003).”