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  • 2020-2024  (19)
  • 2015-2019
  • 2022  (17)
  • 2021  (2)
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  • 1
  • 2
    Publication Date: 2024-03-12
    Description: Zooplankton plays a notable role in ocean biogeochemical cycles. However, it is often simulated as one generic group and top closure term in ocean biogeochemical models. This study presents the description of three zooplankton functional types (zPFTs, micro‐, meso‐ and macrozooplankton) in the ocean biogeochemical model FESOM‐REcoM. In the presented model, microzooplankton is a fast‐growing herbivore group, mesozooplankton is another major consumer of phytoplankton, and macrozooplankton is a slow‐growing group with a low temperature optimum. Meso‐ and macrozooplankton produce fast‐sinking fecal pellets. With three zPFTs, the annual mean zooplankton biomass increases threefold to 210 Tg C. The new food web structure leads to a 25% increase in net primary production and a 10% decrease in export production globally. Consequently, the export ratio decreases from 17% to 12% in the model. The description of three zPFTs reduces model mismatches with observed dissolved inorganic nitrogen and chlorophyll concentrations in the South Pacific and the Arctic Ocean, respectively. Representation of three zPFTs also strongly affects phytoplankton phenology: Fast nutrient recycling by zooplankton sustains higher chlorophyll concentrations in summer and autumn. Additional zooplankton grazing delays the start of the phytoplankton bloom by 3 weeks and controls the magnitude of the bloom peak in the Southern Ocean. As a result, the system switches from a light‐controlled Sverdrup system to a dilution‐controlled Behrenfeld system. Overall, the results suggest that representation of multiple zPFTs is important to capture underlying processes that may shape the response of ecosystems and ecosystem services to on‐going and future environmental change in model projections.
    Description: Plain Language Summary: Zooplankton plays an important role in the ocean food web and biogeochemical cycles. However, it is often represented in very simple forms in mathematical models that are, for example, used to investigate how marine primary productivity will react to climate change. To understand how these models would change when more complicated formulations for zooplankton are used, we present here a new version of the model with three (instead of only one) zooplankton groups. We find that this more complicated representation leads to higher zooplankton biomass, which is closer to observations, and this stimulates growth of phytoplankton since zooplankton also returns nutrients into the system. In addition, zooplankton grazing controls the seasonal cycle of phytoplankton, as we show for one example in the Southern Ocean.
    Description: Key Points: Nutrient recycling by zooplankton stimulates net primary production in the biogeochemical model REcoM‐2. Modeling zooplankton functional types (zPFTs) leads to a switch from a light‐controlled Sverdrup system to a dilution‐controlled Behrenfeld system. Implementing multiple zPFTs improves the modeled zooplankton biomass and zooplankton‐mediated biogeochemical fluxes.
    Description: Helmholtz Young Investigator Group Marine Carbon and Ecosystem Feedbacks in the Earth System [MarESys]
    Description: https://doi.org/10.1594/PANGAEA.779970
    Description: https://doi.org/10.1594/PANGAEA.785501
    Description: https://doi.org/10.1594/PANGAEA.777398
    Description: https://www.nodc.noaa.gov/OC5/woa18/woa18data.html
    Description: http://sites.science.oregonstate.edu/ocean.productivity/index.php
    Description: https://doi.pangaea.de/10.1594/PANGAEA.942192
    Keywords: ddc:577.7 ; Southern Ocean ; zooplankton ; ocean food web ; biogeochemical cycles ; modeling
    Language: English
    Type: doc-type:article
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  • 3
    Publication Date: 2024-03-09
    Description: Increasing upwelling intensity and shoaling of the oxygen minimum zone (OMZ) is projected for Eastern Boundary Upwelling Systems (EBUSs) under ocean warming which may have severe consequences for mesopelagic food webs, trophic transfer, and fish production also in the Humboldt Current Upwelling System (HUS). To improve our mechanistic understanding, from February 23, 2017 until April 14, 2017 we performed a 50 days mesocosm experiment in the northern HUS (off Callao Bay, Peru) and monitored the zooplankton development prior to and following a simulated upwelling event through the addition of deeper water of two different OMZ-influenced subsurface waters to four of in total eight mesocosms. To elucidate plankton dynamics and trophic relationships, we followed the temporal development of the mesozooplankton community in relation to that of phytoplankton, analyzed the fatty acid composition and gut fluorescence of dominant copepods, and determined the stable isotope (SI) and elemental composition (C:N) of dominant zooplankton taxa. Zooplankton samples were collected from the mesocosms over the entire experiment duration using an Apstein net (17 cm diameter, 100 µm mesh) to determine abundance and taxonomic composition of the zooplankton community, and to analyze fatty acid composition, gut fluorescence and elemental composition of dominant zooplankton. Furthermore, abundance and biomass of zooplankton groups was estimated from scanned ZooScan images.
    Keywords: Abundance; Biomass; Climate - Biogeochemistry Interactions in the Tropical Ocean; Coastal Upwelling System in a Changing Ocean; CUSCO; Gut fluorescence; Humboldt Current System; KOSMOS_2017; KOSMOS_2017_Peru; KOSMOS Peru; Lipid; MESO; mesocosm experiment; Mesocosm experiment; Oxygen Minimun zone; SFB754; Stable isotopes; Zooplankton
    Type: Dataset
    Format: application/zip, 5 datasets
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  • 4
    Publication Date: 2024-03-09
    Description: A combined stable isotope and fatty acid trophic biomarker approach was adopted for key zooplankton taxa and higher trophic positions of the northern Humboldt Current System to elucidate the pelagic food-web structure and to better understand trophic interactions. Samples covered an extensive spatial range from 8.5°S to 16°S and a vertical range down to 1,000 m depth. Immediately after each haul, specimens were sorted alive in the lab and apparently live and healthy individuals were stored in vials and deep-frozen at -80°C until further lipid and stable isotope analyses. The comprehensive data set covered over 20 zooplankton taxa and indicated that three biomass-rich crustacean species usually dominated the zooplankton community, i.e., the copepods Calanus chilensis at the surface and Eucalanus inermis in the pronounced oxygen minimum zone and the krill Euphausia mucronata, resulting in an overall low number of major trophic pathways toward anchovies. In addition, the semi-pelagic squat lobster Pleuroncodes monodon appears to play a key role in the benthic-pelagic coupling. By partly feeding on benthic resources and by diel vertical migration, P. monodon provides a unique pathway for returning carbon and energy from the sea floor to the epipelagic layer, increasing the food supply for pelagic fish.
    Keywords: Coastal Upwelling System in a Changing Ocean; CUSCO
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 5
    Publication Date: 2024-03-09
    Description: Abundance and community structure of calanoid copepods of one day (stn. 16; bottom depth 5,433 m) and one night station (stn. 15; bottom depth 5,462 m) were analyzed (Fig. 1). Stratified vertical hauls were carried out within 24 h with a HydroBios Multinet Maxi (0.5 m2 net opening, 9 nets, 150 µm mesh size) from 800 m depth to the surface (strata: 800-700-600-500-400-300-200-100-50-0 m). The filtered water volume was measured with a flowmeter attached to the net opening. After retrieval, samples were preserved in a 4% borax-buffered formaldehyde in seawater solution. Calanoid copepods were sorted according to their developmental stages (copepodids C1-3 and C4/5, adult females and males), counted and identified to genus or, if possible, to species level under a dissecting microscope (Leica MZ12). Rare species (〈100 individuals per sample) were counted from the entire sample. Total length (TL) of up to 100 calanoid individuals per taxonomic category (i.e. family/genus/species) and stage was measured (~6,600 specimens in total). Dry mass (DM) of calanoids was calculated based on the median TL of each taxonomic category. Individual respiration rates were calculated from individual DM and in situ temperatures, which were then converted to carbon units and used to calculate ingestion and egestion rates.
    Keywords: calanoid copepods; South Atlantic Ocean; subtropical area; Zooplankton
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 6
    Publication Date: 2024-03-09
    Description: This dataset shows abundance of zooplankton taxa in individuals per liter as determined by ZooScan. Each data point is one sampling day (date) in one mesocosm (MK). For details on experimental treatments and sampling, refer to Bach et al. 2021 (https://doi.org/10.5194/bg-17-4831-2020) and Ayon et al. 2022 (https://doi.org/10.5194/bg-2022-157). Raw images are stored in https://ecotaxa.obs-vlfr.fr/prj/3784. All taxonomic categories are self-explanatory.
    Keywords: Abundance; Acartia spp.; Biomass; Bivalvia; Branchiostoma spp.; Calanoida; Ceratium spp.; Climate - Biogeochemistry Interactions in the Tropical Ocean; Cnidaria; Coastal Upwelling System in a Changing Ocean; Copepoda; Copepoda, nauplii; Corycaeidae; Crustacea, larvae; CUSCO; Cyclopoida; DATE/TIME; Diatoms, centrales; Gastropoda; Gut fluorescence; Harpacticoida; Hemicyclops spp.; Humboldt Current System; KOSMOS_2017; KOSMOS_2017_Peru; KOSMOS Peru; Lipid; MESO; mesocosm experiment; Mesocosm experiment; Mesocosm label; Noctilucales; Oncaeidae; Oxygen Minimun zone; Paracalanus spp.; Polychaeta; Sample code/label; Sample volume; SFB754; Spionidae; Stable isotopes; Tintinnida; Zooplankton; ZOOSCAN
    Type: Dataset
    Format: text/tab-separated-values, 2430 data points
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  • 7
    Publication Date: 2024-03-09
    Keywords: ANT-XXIX/1; calanoid copepods; Life stage; MSN; Multiple opening/closing net; Number of specimens; Polarstern; Prosome, length; Prosome length, standard deviation; PS81; PS81/015-2; PS81/016-4; South Atlantic Ocean; Species; subtropical area; Zooplankton
    Type: Dataset
    Format: text/tab-separated-values, 1071 data points
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  • 8
    Publication Date: 2024-03-09
    Keywords: Acartia spp., c1-c3; Acartia spp., c4-c5; Acartia spp., female; Acartia spp., male; Aetidaeidae, c1-c3; Aetidaeidae, c4-c5; Aetidaeidae, female; Aetidaeidae, male; Aetidaeus arcuatus, c1-c3; Aetidaeus arcuatus, c4-c5; Aetidaeus arcuatus, female; Aetidaeus arcuatus, male; Aetidaeus armatus, c1-c3; Aetidaeus armatus, c4-c5; Aetidaeus armatus, female; Aetidaeus armatus, male; Aetidaeus australis, c1-c3; Aetidaeus australis, c4-c5; Aetidaeus australis, female; Aetidaeus australis, male; Aetidaeus giesbrechti, c1-c3; Aetidaeus giesbrechti, c4-c5; Aetidaeus giesbrechti, female; Aetidaeus giesbrechti, male; Aetidaeus spp., c1-c3; Aetidaeus spp., c4-c5; Aetidaeus spp., female; Aetidaeus spp., male; Aetideopsis carinata, c1-c3; Aetideopsis carinata, c4-c5; Aetideopsis carinata, female; Aetideopsis carinata, male; Aetideopsis spp., c1-c3; Aetideopsis spp., c4-c5; Aetideopsis spp., female; Aetideopsis spp., male; Amallothrix spp., c1-c3; Amallothrix spp., c4-c5; Amallothrix spp., female; Amallothrix spp., male; ANT-XXIX/1; Augaptilidae, c1-c3; Augaptilidae, c4-c5; Augaptilidae, female; Augaptilidae, male; Augaptilus anceps, c1-c3; Augaptilus anceps, c4-c5; Augaptilus anceps, female; Augaptilus anceps, male; Augaptilus longicaudatus, c1-c3; Augaptilus longicaudatus, c4-c5; Augaptilus longicaudatus, female; Augaptilus longicaudatus, male; Augaptilus megalurus, c1-c3; Augaptilus megalurus, c4-c5; Augaptilus megalurus, female; Augaptilus megalurus, male; Augaptilus spinifrons, c1-c3; Augaptilus spinifrons, c4-c5; Augaptilus spinifrons, female; Augaptilus spinifrons, male; Augaptilus spp., c1-c3; Augaptilus spp., c4-c5; Augaptilus spp., female; Augaptilus spp., male; Calanidae, c1-c3; Calanidae, c4-c5; Calanidae, female; Calanidae, male; Calanoides natalis, c1-c3; Calanoides natalis, c4-c5; Calanoides natalis, female; Calanoides natalis, male; Calocalanus spp., c1-c3; Calocalanus spp., c4-c5; Calocalanus spp., female; Calocalanus spp., male; Candacia bipinnata, c1-c3; Candacia bipinnata, c4-c5; Candacia bipinnata, female; Candacia bipinnata, male; Candacia curta, c1-c3; Candacia curta, c4-c5; Candacia curta, female; Candacia curta, male; Candacia elongata, c1-c3; Candacia elongata, c4-c5; Candacia elongata, female; Candacia elongata, male; Candacia ethiopica, c1-c3; Candacia ethiopica, c4-c5; Candacia ethiopica, female; Candacia ethiopica, male; Candacia longimana, c1-c3; Candacia longimana, c4-c5; Candacia longimana, female; Candacia longimana, male; Candacia spp., c1-c3; Candacia spp., c4-c5; Candacia spp., female; Candacia spp., male; Centropages bradyi, c1-c3; Centropages bradyi, c4-c5; Centropages bradyi, female; Centropages bradyi, male; Cephalophanes spp., c1-c3; Cephalophanes spp., c4-c5; Cephalophanes spp., female; Cephalophanes spp., male; Clausocalanus spp., c1-c3; Clausocalanus spp., c4-c5; Clausocalanus spp., female; Clausocalanus spp., male; Comment; Copepoda; Ctenocalanus spp., c1-c3; Ctenocalanus spp., c4-c5; Ctenocalanus spp., female; Ctenocalanus spp., male; Delibus spp., c1-c3; Delibus spp., c4-c5; Delibus spp., female; Delibus spp., male; Depth, bottom/max; Depth, top/min; DEPTH, water; Disco spp., c1-c3; Disco spp., c4-c5; Disco spp., female; Disco spp., male; Euaugaptilus spp., c1-c3; Euaugaptilus spp., c4-c5; Euaugaptilus spp., female; Euaugaptilus spp., male; Eucalanus hyalinus, c1-c3; Eucalanus hyalinus, c4-c5; Eucalanus hyalinus, female; Eucalanus hyalinus, male; Euchaeta marina, c1-c3; Euchaeta marina, c4-c5; Euchaeta marina, female; Euchaeta marina, male; Euchaeta spp., c1-c3; Euchaeta spp., c4-c5; Euchaeta spp., female; Euchaeta spp., male; Euchaetidae, c1-c3; Euchaetidae, c4-c5; Euchaetidae, female; Euchaetidae, male; Euchirella pulchra, c1-c3; Euchirella pulchra, c4-c5; Euchirella pulchra, female; Euchirella pulchra, male; Euchirella splendes, c1-c3; Euchirella splendes, c4-c5; Euchirella splendes, female; Euchirella splendes, male; Euchirella spp., c1-c3; Euchirella spp., c4-c5; Euchirella spp., female; Euchirella spp., male; Event label; Farrania frigida, c1-c3; Farrania frigida, c4-c5; Farrania frigida, female; Farrania frigida, male; Gaetanus brevicornis, c1-c3; Gaetanus brevicornis, c4-c5; Gaetanus brevicornis, female; Gaetanus brevicornis, male; Gaetanus cf. pileatus, c1-c3; Gaetanus cf. pileatus, c4-c5; Gaetanus cf. pileatus, female; Gaetanus cf. pileatus, male; Gaetanus kruppii, c1-c3; Gaetanus kruppii, c4-c5; Gaetanus kruppii, female; Gaetanus kruppii, male; Gaetanus spp., c1-c3; Gaetanus spp., c4-c5; Gaetanus spp., female; Gaetanus spp., male; Haloptilus cf. longicirrus, c1-c3; Haloptilus cf. longicirrus, c4-c5; Haloptilus cf. longicirrus, female; Haloptilus cf. longicirrus, male; Haloptilus cf. oxycephalus, c1-c3; Haloptilus cf. oxycephalus, c4-c5; Haloptilus cf. oxycephalus, female; Haloptilus cf. oxycephalus, male; Haloptilus spp., c1-c3; Haloptilus spp., c4-c5; Haloptilus spp., female; Haloptilus spp., male; Heterorhabdidae, c1-c3; Heterorhabdidae, c4-c5; Heterorhabdidae, female; Heterorhabdidae, male; Heterorhabdus cf. lobatus, c1-c3; Heterorhabdus cf. lobatus, c4-c5; Heterorhabdus cf. lobatus, female; Heterorhabdus cf. lobatus, male; Heterorhabdus spp., c1-c3; Heterorhabdus spp., c4-c5; Heterorhabdus spp., female; Heterorhabdus spp., male; Lophothrix humilifrons, c1-c3; Lophothrix humilifrons, c4-c5; Lophothrix humilifrons, female; Lophothrix humilifrons, male; Lophothrix spp., c1-c3; Lophothrix spp., c4-c5; Lophothrix spp., female; Lophothrix spp., male; Lucicutia gaussae, c1-c3; Lucicutia gaussae, c4-c5; Lucicutia gaussae, female; Lucicutia gaussae, male; Lucicutia longicornis, c1-c3; Lucicutia longicornis, c4-c5; Lucicutia longicornis, female; Lucicutia longicornis, male; Lucicutia ovalis, c1-c3; Lucicutia ovalis, c4-c5; Lucicutia ovalis, female; Lucicutia ovalis, male; Lucicutia spp., c1-c3; Lucicutia spp., c4-c5; Lucicutia spp., female; Lucicutia spp., male; Mecynocera clausi, c1-c3; Mecynocera clausi, c4-c5; Mecynocera clausi, female; Mecynocera clausi, male; Megacalanus princeps, c1-c3; Megacalanus princeps, c4-c5; Megacalanus princeps, female; Megacalanus princeps, male; Mesocalanus tenuicornis, c1-c3; Mesocalanus tenuicornis, c4-c5; Mesocalanus tenuicornis, female; Mesocalanus tenuicornis, male; Metridia brevicauda, c1-c3; Metridia brevicauda, c4-c5; Metridia brevicauda, female; Metridia brevicauda, male; Metridia discreta, c1-c3; Metridia discreta, c4-c5; Metridia discreta, female; Metridia discreta, male; Metridia effusa, c1-c3; Metridia effusa, c4-c5; Metridia effusa, female; Metridia effusa, male; Metridia lucens, c1-c3; Metridia lucens, c4-c5; Metridia lucens, female; Metridia lucens, male; Metridia princeps, c1-c3; Metridia princeps, c4-c5; Metridia princeps, female; Metridia princeps, male; Metridia spp., c1-c3; Metridia spp., c4-c5; Metridia spp., female; Metridia spp., male; Metridia venusta, c1-c3; Metridia venusta, c4-c5; Metridia venusta, female; Metridia venusta, male; Metridinidae, c1-c3; Metridinidae, c4-c5; Metridinidae, female; Metridinidae, male; Microcalanus spp., c1-c3; Microcalanus spp., c4-c5; Microcalanus spp., female; Microcalanus spp., male; Mimocalanus spp., c1-c3; Mimocalanus spp., c4-c5; Mimocalanus spp., female; Mimocalanus spp., male; Monacilla spp., c1-c3; Monacilla spp., c4-c5; Monacilla spp., female; Monacilla spp., male; Monacilla typica, c1-c3; Monacilla typica, c4-c5; Monacilla typica, female; Monacilla typica, male; MSN; Multiple opening/closing net; Nannocalanus minor, c1-c3; Nannocalanus minor, c4-c5; Nannocalanus minor, female; Nannocalanus minor, male; Neocalanus gracilis, c1-c3; Neocalanus gracilis, c4-c5; Neocalanus gracilis, female; Neocalanus gracilis, male; Neocalanus robustior, c1-c3; Neocalanus robustior, c4-c5; Neocalanus robustior, female; Neocalanus robustior, male; Nullosetigera impar, c1-c3; Nullosetigera impar, c4-c5; Nullosetigera impar, female; Nullosetigera impar, male; Nullosetigera spp., c1-c3; Nullosetigera spp., c4-c5; Nullosetigera spp., female;
    Type: Dataset
    Format: text/tab-separated-values, 9342 data points
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  • 9
    Publication Date: 2024-04-20
    Description: Males of the four crab species Percnon affine (H. Milne Edwards, 1853), Grapsus albolineatus (Latreille in Milbert, 1812), Orisarma intermedium (Schubart &Ng, 2020), and Geothelphusa albogilva (Shy, Ng & Yu, 1994), were collected in the southern part of Taiwan in May 2007. Individuals were starved for 12 days and midgut glands were dissected before and after the starvation period. Midgut glands were lyophilized and total lipids were extracted with dichloromethane:methanol (2:1 per volume) and an aqueous solution of 0.88% KCl. Extracted lipid mass was determined gravimetrically. Lipid classes were separated and quantified using Thin-Layer Chromatography with an integrated flame ionization detector (MK-5 TLC/FID analyzer, Iatron Laboratories). Lipids were converted to fatty acids methyl esters (FAME) by applying methanol containing 3% concentrated sulfuric acid. FAMEs were quantified by gas chromatography equipped with a DB-FFAP column, a programmable temperature vaporizer injector, and a flame ionization detector. Helium was used as carrier gas. Fatty acids were identified by retention times and by using fish oil standard (Marinol). Data are supplement to: Stumpp et al (2021) Dietary preferences of brachyuran crabs from Taiwan for marine or terrestrial food sources: evidence based on fatty acid trophic markers accepted for publication in Frontiers in Zoology
    Keywords: algae; Decapoda; fatty acids; lipids; midgut gland; triacylglycerols; trophic relationships; vascular plants
    Type: Dataset
    Format: application/vnd.openxmlformats-officedocument.spreadsheetml.sheet, 202.7 kBytes
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  • 10
    Publication Date: 2024-04-24
    Description: Fatty acids were analyzed by gas chromatography using a DB-FFAP column of 30 m length and 0.25 mm inner diameter and a programmable temperature vaporizer injector. Following the trophic biomarker concept, the fatty acids 16:0, 20:5(n-3) and 22:6(n-3) were classified as typical components of biomembranes. High levels of 16:1(n−7) as well as 16:4(n−1) and 18:1(n−7) were used as diatom markers and 18:4(n−3) as fatty acid marker for dinoflagellates. The fatty acid 18:1(n-9) indicates carnivorous feeding. A carnivory index was applied based on the fatty acid ratio 18:1(n−9) / [16:1(n−7) + 16:4(n−1) + 18:1(n−7) + 18:4(n−3) + 18:1(n−9)] to reflect the proportion of carnivorous compared to herbivorous feeding in an organism. Fatty acid compositions of zooplankton and fish were taxon-specific and did not depend on sampling area or depth. Most species showed a dominance of typical membrane fatty acids, e.g., 16:0, 20:5(n-3) and 22:6(n-3). The dominant copepod Calanus chilensis had a low carnivory index and elevated amounts of diatom fatty acid markers which point to a predominantly herbivorous feeding. Among the krill species, Euphausia mucronata had the lowest carnivory index compared to the other euphausiids indicating a more herbivorous feeding. The squat lobster Pleuroncodes monodon had a significantly lower carnivory ratio compared to the deep-sea decapods Gennadas sp. and Acanthephyra sp. emphasizing its different trophic role compared to other decapods.
    Keywords: 6,9,12,15-Hexadecatetraenoic acid of total fatty acids; ACS; all-cis-4,7,10,13,16,19-Docosahexaenoic acid of total fatty acids; all-cis-5,8,11,14,17-Eicosapentaenoic acid of total fatty acids; all-cis-5,8,11,14-Eicosatetraenoic acid of total fatty acids; all-cis-8,11,14-Octadecatrienoic acid of total fatty acids; all-cis-9,12-Octadecadienoic acid of total fatty acids; cis-11-Docosenoic acid of total fatty acids; cis-11-Icosenoic acid of total fatty acids; cis-11-Octadecenoic acid of total fatty acids (IUPAC: Octadec-11-enoic acid); cis-11-Octadecenol of total fatty alcohols; cis-15-Tetracosenoic acid of total fatty acids; cis-9-Hexadecenoic acid of total fatty acids (IUPAC: (9Z)-hexadec-9-enoic acid); cis-9-Hexadecenol of total fatty alcohols; cis-9-Octadecenoic acid of total fatty acids (IUPAC: Octadec-9-enoic acid); cis-9-Octadecenol of total fatty alcohols; Coastal Upwelling System in a Changing Ocean; CUSCO; CUSCO-1; Date/Time of event; Depth, bottom/max; Depth, top/min; Docosenol of total fatty alcohols; Eicosenol of total fatty alcohols; Event label; Gas chromatography; Hexadecanoic acid of total fatty acids; Hexadecanol of total fatty alcohols; IKMT; Individual dry mass; Isaac-Kid-Midwater Trawl; Latitude of event; Life stage; Lipids; Longitude of event; Maria S. Merian; Microstructure Profiler; MSM80; MSM80_102-4; MSM80_13-4; MSM80_15-5; MSM80_1-6; MSM80_16-4; MSM80_18-4; MSM80_18-7; MSM80_1-9; MSM80_20-4; MSM80_30-4; MSM80_31-4; MSM80_31-7; MSM80_34-4; MSM80_40-5; MSM80_4-6; MSM80_46-15; MSM80_46-20; MSM80_46-23; MSM80_49-6; MSM80_56-5; MSM80_58-4; MSM80_67-4; MSM80_68-5; MSM80_68-6; MSM80_7-4; MSM80_74-4; MSM80_7-8; MSM80_85-3; MSM80_94-5; MSM80_95-4; MSN; MSSP; Multiple opening/closing net; Octadecanoic acid of total fatty acids; Octadecanol of total fatty alcohols; Optical Profiler, ACS; Order; Phytanic acid of total fatty acids; Sample ID; Species; Station label; Tetradecanoic acid of total fatty acids; Tetradecanol of total alcohols; Wax esters
    Type: Dataset
    Format: text/tab-separated-values, 4235 data points
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