Trophic marker composition of Arctic zooplankton and Polar cod sampled under sea ice and throughout the water column of the Central Arctic Ocean during the MOSAiC expedition (2019/2020)

At the basis of the marine Arctic food web, there are several carbon sources including ice-associated (sympagic) algae that live primarily in sea ice, melt ponds or underneath sea ice; pelagic algae that live primarily in open waters; terrestrial detritus that got incorporated into sea ice forming on the Siberian Shelf and being transported with the transpolar drift across the Central Arctic Ocean (CAO); and detritus that derives with currents from the Atlantic ocean. Copepods and amphipods are diverse and often biomass-dominant zooplankton groups in the CAO that include taxa specialised in feeding on algae and small heterotrophs, on sinking detritus or other zooplankton. Gelatinous (cnidaria, appendicularia) and semi-gelatinous (chaetognaths) taxa, ostracods, pteropods, euphausiids and pelagic decapods are other important zooplankton groups in the CAO that likewise feed on a range of food sources. With the loss of Arctic sea ice, the relative importance of ice-associated carbon in the Arctic food web became a central research topic, and multiple trophic marker approaches have been developed to distinguish between pelagic and sympagic carbon transfer to higher trophic levels.
During the MOSAiC expedition in the CAO (2019-2020), zooplankton was sampled weekly to fortnightly. A range of nets were used to sample either horizontally underneath the sea ice or vertically from a maximum depth of 2000 m to the surface. Onboard, abundant zooplankton taxa were sorted from each catch, photographed, rinsed with freshwater to remove salt and frozen at -80 degrees Celsius for subsequent analysis of their total dry mass (DM), lipid content, lipid classes and a suite of trophic markers, including bulk stable isotopes (BSI), phytosterols (PS), total fatty acids (TFA), total fatty alcohols (TFAlc), highly-branched isoprenoids (HBI) and the carbon isotopic composition of key FA and FAlc (CSIA-FA; CSIA-FAlc). We had ~10 target species that were sampled in all seasons (the copepods C. hyperboreus, C. glacialis, Metridia longa, the ice amphipods Apherusa glacialis and Eusirus spp., the pelagic amphipods Themisto abyssorum and T. libellula, the euphausiid Thysanoessa spp., chaetognaths and the shrimp H. glacialis). Further zooplankton taxa were collected when available in the net catches and time permitted. Additionally, Polar cod was collected in early and late summer.
The initial separation of the various trophic markers was carried out at the University of Plymouth. After estimating the total DM, subsamples for BSI were sent to the Littoral, Environment and Societies Joint Research Unit stable isotope facility (CNRS - University of La Rochelle, France) for analysis. Three internal standards were added to the samples used for lipid analysis to quantify the TFA, TFAlc, PS and HBI content. As a first step, the total lipid content of the animals was extracted in dichloromethane : methanol. The lipid samples were split into two equal subsamples, one was sent to the Alfred-Wegener-Institute (AWI) in Bremerhaven/Germany for FA and FAlc analyses and the second was used for PS and HBI analyses in Plymouth.
This dataset is linked to a manuscript that assesses trophic relationships in the CAO to understand the carbon fluxes in the current Arctic food web and to predict potential changes in a future ice-free Arctic.