Fatty acid trophic markers in the pelagic marine environment.
By J. Dalsgaard, Michael A. St. John, G. Kattner, D. Müller-Navarra, W. Hagen. Advances in Marine Biology, 2003
1,545 citations recorded by the source corpus.
Subfields: Ecology, Global and Planetary Change, Oceanography
View Paper: https://www.semanticscholar.org/paper/0d930f52869c26826389b988b5d1347fa3759457
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecology
- Michael T. Brett
- S. Iverson
- M. Kainz
- Jack J. Middelburg
- R. Scheibling
- J. Kelly
- S. Taipale
- A. Atkinson
In Global and Planetary Change
In Oceanography
- Michael T. Brett
- Jack J. Middelburg
- M. Kainz
- S. Falk‐Petersen
- D. Müller-Navarra
- S. Iverson
- G. Kattner
- M. Gibbons
Citations in the corpus
- Trophic interactions of macro-zooplankton (krill and amphipods) in the Marginal Ice Zone of the Barents Sea (2008, background): “M. longa is a deeper-living species than Calanus spp. (4100 m) and is known to be quite important, both in abundance and biomass in the central Arctic (Mumm et al., 1998).”
- Essential Biomolecules in Food Webs (2019, background): “, 1997), and semi-quantitatively in food webs in marine pelagial (Dalsgaard et al., 2003) and benthos (Kelly and Scheibling, 2012).”
- Trace me if you can: the use of intrinsic biogeochemical markers in marine top predators (2012, background): “Prey fatty acids are deposited into consumer adipose tissue with little modification and, in a predictable way, providing insights into the pathways of energy and nutrient transfer (Dalsgaard et al. 2003; Iverson 2009; Williams and Buck 2010).”
- Autochthonous and allochthonous contributions to mesozooplankton diet in a tidal river and estuary: Integrating carbon isotope and fatty acid constraints (2009, background): “Assimilation efficiencies may indeed be fatty acid-specific, and de novo synthesis of (mostly C-20 and C-22) lipids has been reported for calanoid copepods (Dalsgaard et al. 2003).”
- The importance of ice algae‐produced carbon in the central Arctic Ocean ecosystem: Food web relationships revealed by lipid and stable isotope analyses (2016, background): “Dinophyceae (simplified to dinoflagellates) are often more abundant in the water column and contain high amounts of the FA 22:6n-3 and C18 PUFAs (e.g., Dalsgaard et al. 2003).”
- Distribution of lipids and fatty acids in corals by their taxonomic position and presence of zooxanthellae (2010, background): “Different food sources have a specific lipid composition (Dalsgaard et al. 2003).”
- Daphnia fatty acid composition reflects that of their diet (2006, background): “Most of what is known about dietary impacts on zooplankton fatty acid composition is from the marine copepod literature (Dalsgaard et al. 2003).”
- Lipids and life strategy of Arctic Calanus (2009, background): “The diatom FATM 16:1(n 7), 16PUFAs and 20:5(n 3) were very low (10 15”
- Feeding and overwintering of Antarctic krill across its major habitats: The role of sea ice cover, water depth, and phytoplankton abundance (2014, methodology): “These fatty acids have a specific structural role in higher organisms but are not sufficiently synthesized within the body and have therefore to be taken up with the food (Dalsgaard et al. 2003).”
- Diet-specific biomarkers show that high-quality phytoplankton fuels herbivorous zooplankton in large boreal lakes (2014, background): “Fatty acids are commonly used as trophic biomarkers (Dalsgaard et al., 2003), but are rarely used for quantitative estimation of consumer diets.”
- Fatty acids as dietary tracers in benthic food webs (2012, positive): “FA biosynthesis in heterotrophic bacteria produces oddnumbered and branched FAs such as 15:0, 17:0, 15:1, 17:1, and iso- and anteiso-branched SFAs (Dalsgaard et al. 2003).”