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Distribution, associations and role in the biological carbon pump of Pyrosoma atlanticum (Tunicata, Thaliacea) off Cabo Verde, NE Atlantic

  • 1.

    Pugh, P. Gelatinous zooplankton: the forgotten fauna. Sci. Prog. 14, 67–78 (1989).

    Google Scholar 

  • 2.

    Robison, B. H. Deep pelagic biology. J. Exp. Mar. Biol. Ecol. 300, 253–272. https://doi.org/10.1016/j.jembe.2004.01.012 (2004).

    Article 

    Google Scholar 

  • 3.

    Condon, R. H. et al. Questioning the rise of gelatinous zooplankton in the world’s oceans. Bioscience 62, 160–169. https://doi.org/10.1525/bio.2012.62.2.9 (2012).

    Article 

    Google Scholar 

  • 4.

    Haddock, S. H. D. A golden age of gelata: past and future research on planktonic ctenophores and cnidarians. Hydrobiologia 530, 549–556. https://doi.org/10.1007/s10750-004-2653-9 (2004).

    Article 

    Google Scholar 

  • 5.

    Lebrato, M. et al. Sinking of gelatinous zooplankton biomass increases deep carbon transfer efficiency globally. Glob. Biogeochem. Cycles 33, 1764–1783. https://doi.org/10.1029/2019GB006265 (2019).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 6.

    Luo, J. Y. et al. Gelatinous zooplankton-mediated carbon flows in the global oceans: a data-driven modeling study. Glob. Biogeochem. Cycles https://doi.org/10.1029/2020GB006704 (2020).

    Article 

    Google Scholar 

  • 7.

    Lucas, C. H. et al. Gelatinous zooplankton biomass in the global oceans: geographic variation and environmental drivers. Glob. Ecol. Biogeogr. 23, 701–714. https://doi.org/10.1111/geb.12169 (2014).

    Article 

    Google Scholar 

  • 8.

    Robison, B. H. Conservation of deep pelagic biodiversity. Conserv. Biol. 23, 847–858 (2009).

    Article 

    Google Scholar 

  • 9.

    Décima, M., Stukel, M. R., López-López, L. & Landry, M. R. The unique ecological role of pyrosomes in the Eastern Tropical Pacific. Limnol. Oceanogr. 64, 728–743. https://doi.org/10.1002/lno.11071 (2019).

    ADS 
    Article 

    Google Scholar 

  • 10.

    Henschke, N. et al. Large vertical migrations of Pyrosoma atlanticum play an important role in active carbon transport. J. Geophys. Res. Biogeosci. https://doi.org/10.1029/2018jg004918 (2019).

    Article 

    Google Scholar 

  • 11.

    Sutherland, K. R., Sorensen, H. L., Blondheim, O. N., Brodeur, R. D. & Galloway, A. W. E. Range expansion of tropical pyrosomes in the northeast Pacific Ocean. Ecology 99, 2397–2399. https://doi.org/10.1002/ecy.2429 (2018).

    Article 
    PubMed 

    Google Scholar 

  • 12.

    Perissinotto, R., Mayzaud, P., Nichols, P. D. & Labat, J. P. Grazing by Pyrosoma atlanticum (Tunicata, Thaliacea) in the south Indian Ocean. Mar. Ecol. Prog. Ser. 330, 1–11 (2007).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 13.

    van Soest, R. W. M. A monograph of the order Pyrosomatida (Tunicata, Thaliacea). J. Plankton Res. 3, 603–631. https://doi.org/10.1093/plankt/3.4.603 (1981).

    Article 

    Google Scholar 

  • 14.

    Drits, A. V., Arashkevich, E. G. & Semenova, T. N. Pyrosoma atlanticum (Tunicata, Thaliacea): grazing impact on phytoplankton standing stock and role in organic carbon flux. J. Plankton Res. 14, 799–809. https://doi.org/10.1093/plankt/14.6.799 (1992).

    Article 

    Google Scholar 

  • 15.

    Lebrato, M. & Jones, D. O. B. Mass deposition event of Pyrosoma atlanticum carcasses off Ivory Coast (West Africa). Limnol. Oceanogr. 54, 1197–1209. https://doi.org/10.4319/lo.2009.54.4.1197 (2009).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 16.

    Lebrato, M. et al. Sinking jelly-carbon unveils potential environmental variability along a continental margin. PLoS ONE 8, e82070. https://doi.org/10.1371/journal.pone.0082070 (2013).

    ADS 
    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 17.

    Archer, S. K. et al. Pyrosome consumption by benthic organisms during blooms in the northeast Pacific and Gulf of Mexico. Ecology 99, 981–984. https://doi.org/10.1002/ecy.2097 (2018).

    Article 
    PubMed 

    Google Scholar 

  • 18.

    Harbison, G. R. in The Biology of Pelagic Tunicates (ed Q. Bone) Ch. 12, 186–214 (Oxford University Press, 1998).

  • 19.

    James, G. D. & Stahl, J. C. Diet of southern Buller’s albatross (Diomedea bulleri bulleri) and the importance of fishery discards during chick rearing. NZ J. Mar. Freshwat. Res. 34, 435–454. https://doi.org/10.1080/00288330.2000.9516946 (2000).

    Article 

    Google Scholar 

  • 20.

    Hedd, A. & Gales, R. The diet of shy albatrosses (Thalassarche cauta) at Albatross Island, Tasmania. J. Zool. 253, 69–90. https://doi.org/10.1017/S0952836901000073 (2001).

    Article 

    Google Scholar 

  • 21.

    Brodeur, R. et al. An unusual gelatinous plankton event in the NE Pacific: the great pyrosome bloom of 2017. PICES Press 26, 22–27 (2018).

    Google Scholar 

  • 22.

    Childerhouse, S., Dix, B. & Gales, N. Diet of New Zealand sea lions at the Auckland Islands. Wildl. Res. 28, 291–298. https://doi.org/10.1071/WR00063 (2001).

    Article 

    Google Scholar 

  • 23.

    Lindsay, D., Hunt, J. & Hayashi, K.-I. Associations in the midwater zone: The penaeid shrimp Funchalia sagamiensis FUJINO 1975 and pelagic tunicates (Order: Pyrosomatida). Marine Freshwater Behav. Phys. 34, 157–170. https://doi.org/10.1080/10236240109379069 (2001).

    Article 

    Google Scholar 

  • 24.

    Andersen, V. in The Biology of Pleagic Tunicates (ed Q. Bone) Ch. 7, 125–137 (Oxford University Press, 1998).

  • 25.

    Madin, L. P. Production, composition and sedimentation of salp fecal pellets in oceanic waters. Mar. Biol. 67, 39–45. https://doi.org/10.1007/BF00397092 (1982).

    Article 

    Google Scholar 

  • 26.

    Thomsen, P. F. & Willerslev, E. Environmental DNA: an emerging tool in conservation for monitoring past and present biodiversity. Biol. Cons. 183, 4–18. https://doi.org/10.1016/j.biocon.2014.11.019 (2015).

    Article 

    Google Scholar 

  • 27.

    Andruszkiewicz, E. A. et al. Biomonitoring of marine vertebrates in Monterey Bay using eDNA metabarcoding. PLoS ONE 12, e0176343. https://doi.org/10.1371/journal.pone.0176343 (2017).

    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 28.

    Doty, M. S. & Oguri, M. The Island mass effect. ICES J. Mar. Sci. 22, 33–37. https://doi.org/10.1093/icesjms/22.1.33 (1956).

    Article 

    Google Scholar 

  • 29.

    Gove, J. M. et al. Near-island biological hotspots in barren ocean basins. Nat. Commun. 7, 10581. https://doi.org/10.1038/ncomms10581 (2016).

    ADS 
    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 30.

    Faye, S., Lazar, A., Sow, B. & Gaye, A. A model study of the seasonality of sea surface temperature and circulation in the Atlantic North-eastern tropical upwelling system. Front. Phys. https://doi.org/10.3389/fphy.2015.00076 (2015).

    Article 

    Google Scholar 

  • 31.

    Schütte, F., Brandt, P. & Karstensen, J. Occurrence and characteristics of mesoscale eddies in the tropical northeastern Atlantic Ocean. Ocean Sci. 12, 663–685. https://doi.org/10.5194/os-12-663-2016 (2016).

    ADS 
    Article 

    Google Scholar 

  • 32.

    Gilly, W. F., Beman, J. M., Litvin, S. Y. & Robison, B. H. Oceanographic and biological effects of shoaling of the oxygen minimum zone. Ann. Rev. Mar. Sci. 5, 393–420. https://doi.org/10.1146/annurev-marine-120710-100849 (2013).

    Article 
    PubMed 

    Google Scholar 

  • 33.

    Schütte, F. et al. Characterization of “dead-zone” eddies in the eastern tropical North Atlantic. Biogeosciences 13, 5865–5881. https://doi.org/10.5194/bg-13-5865-2016 (2016).

    ADS 
    Article 

    Google Scholar 

  • 34.

    GEOMAR Helmholtz-Zentrum für Ozeanforschung. CVOO Cape Verde Ocean Observatory, http://cvoo.geomar.de/ (n.d.).

  • 35.

    NASA Goddard Space Flight Center, O. E. L., Ocean Biology Processing Group. Moderate-resolution Imaging Spectroradiometer (MODIS) Aqua Chlorophyll Data. https://doi.org/10.5067/AQUA/MODIS/L3B/CHL/2018 (2019).

  • 36.

    Hoving, H. J. et al. The Pelagic in situ observation system (PELAGIOS) to reveal biodiversity, behavior, and ecology of elusive oceanic fauna. Ocean Sci. 15, 1327–1340. https://doi.org/10.5194/os-15-1327-2019 (2019).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 37.

    Schlining, B. & Stout, N. MBARI’s Video Annotation and reference system. Vol. 2006 (2006).

  • 38.

    O’Loughlin, J. H. et al. Implications of Pyrosoma atlanticum range expansion on phytoplankton standing stocks in the Northern California Current. Prog. Oceanogr. 188, 102424. https://doi.org/10.1016/j.pocean.2020.102424 (2020).

    Article 

    Google Scholar 

  • 39.

    Al-Mutairi, H. & Landry, M. R. Active export of carbon and nitrogen at Station ALOHA by diel migrant zooplankton. Deep Sea Res. Part II Top. Stud. Ocean. 48, 2083–2103. https://doi.org/10.1016/S0967-0645(00)00174-0 (2001).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 40.

    Mayzaud, P., Boutoute, M., Gasparini, S., Mousseau, L. & Lefevre, D. Respiration in marine zooplankton—the other side of the coin: CO2 production. Limnol. Oceanogr. 50, 291–298. https://doi.org/10.4319/lo.2005.50.1.0291 (2005).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 41.

    GEOMAR Helmholtz-Zentrum für Ozeanforschung, Hissmann, K. & Schauer, J. Manned submersible JAGO. J. Large-Scale Res. Facil. 3, 1–12, https://doi.org/10.17815/jlsrf-3-157 (2017).

  • 42.

    Lavaniegos, B. E. & Ohman, M. D. Long-term changes in pelagic tunicates of the California current. Deep Sea Res. Part II Top. Stud. Ocen. 50, 2473–2498. https://doi.org/10.1016/S0967-0645(03)00132-2 (2003).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 43.

    GEBCO Compilation Group. GEBCO 2019 Grid. https://doi.org/10.5285/836f016a-33be-6ddc-e053-6c86abc0788e (2019).

  • 44.

    Schram, J. B., Sorensen, H. L., Brodeur, R. D., Galloway, A. W. E. & Sutherland, K. R. Abundance, distribution, and feeding ecology of Pyrosoma atlanticum in the Northern California current. Mar. Ecol. Prog. Ser. 651, 97–110 (2020).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 45.

    Goy, J. Vertical migration of zooplankton. Résultats des Campagnes à la mer, GNEXO 13, 71–73 (1977).

    Google Scholar 

  • 46.

    Andersen, V. & Sardou, J. Pyrosoma atlanticum (Tunicata, Thaliacea): diel migration and vertical distribution as a function of colony size. J. Plankton Res. 16, 337–349. https://doi.org/10.1093/plankt/16.4.337 (1994).

    Article 

    Google Scholar 

  • 47.

    Andersen, V., Sardou, J. & Nival, P. The diel migrations and vertical distributions of zooplankton and micronekton in the Northwestern Mediterranean Sea. 2. Siphonophores, hydromedusae and pyrosomids. J. Plankton Res. 14, 1155–1169. https://doi.org/10.1093/plankt/14.8.1155 (1992).

    Article 

    Google Scholar 

  • 48.

    Roe, H. S. J. et al. Great Meteor East: a biological characterisation (Wormley, 1987).

    Google Scholar 

  • 49.

    Williamson, C. E., Fischer, J. M., Bollens, S. M., Overholt, E. P. & Breckenridge, J. K. Toward a more comprehensive theory of zooplankton diel vertical migration: Integrating ultraviolet radiation and water transparency into the biotic paradigm. Limnol. Oceanogr. 56, 1603–1623. https://doi.org/10.4319/lo.2011.56.5.1603 (2011).

    ADS 
    Article 

    Google Scholar 

  • 50.

    Bianchi, D., Galbraith, E. D., Carozza, D. A., Mislan, K. A. S. & Stock, C. A. Intensification of open-ocean oxygen depletion by vertically migrating animals. Nat. Geosci. 6, 545–548. https://doi.org/10.1038/ngeo1837 (2013).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 51.

    Purcell, J. et al. in Coastal Hypoxia: Consequences for Living Resources and Ecosystems Vol. 58 77–100 (2001).

  • 52.

    Neitzel, P. The impact of the oxygen minimum zone on the vertical distribution and abundance of gelatinous macrozooplankton in the Eastern Tropical Atlantic, Christian-Albrechts-Universität Kiel, (2017).

  • 53.

    Hoving, H. J. T. et al. In situ observations show vertical community structure of pelagic fauna in the eastern tropical North Atlantic off Cape Verde. Sci. Rep. 10, 21798. https://doi.org/10.1038/s41598-020-78255-9 (2020).

    ADS 
    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 54.

    Thuesen, E. V. et al. Intragel oxygen promotes hypoxia tolerance of scyphomedusae. J. Exp. Biol. 208, 2475. https://doi.org/10.1242/jeb.01655 (2005).

    Article 
    PubMed 

    Google Scholar 

  • 55.

    Keeling, R. F., Körtzinger, A. & Gruber, N. Ocean deoxygenation in a warming world. Ann. Rev. Mar. Sci. 2, 199–229. https://doi.org/10.1146/annurev.marine.010908.163855 (2009).

    Article 

    Google Scholar 

  • 56.

    Wiebe, P. H., Madin, L. P., Haury, L. R., Harbison, G. R. & Philbin, L. M. Diel vertical migration by Salpa aspera and its potential for large-scale particulate organic matter transport to the deep-sea. Mar. Biol. 53, 249–255. https://doi.org/10.1007/BF00952433 (1979).

    Article 

    Google Scholar 

  • 57.

    Ariza, A., Garijo, J. C., Landeira, J. M., Bordes, F. & Hernández-León, S. Migrant biomass and respiratory carbon flux by zooplankton and micronekton in the subtropical northeast Atlantic Ocean (Canary Islands). Prog. Oceanogr. 134, 330–342. https://doi.org/10.1016/j.pocean.2015.03.003 (2015).

    ADS 
    Article 

    Google Scholar 

  • 58.

    Hernández-León, S. et al. Zooplankton and micronekton active flux across the tropical and subtropical Atlantic Ocean. Front. Mar. Sci. https://doi.org/10.3389/fmars.2019.00535 (2019).

    Article 

    Google Scholar 

  • 59.

    Kiko, R. et al. Zooplankton-mediated fluxes in the eastern tropical North Atlantic. Front. Mar. Sci. https://doi.org/10.3389/fmars.2020.00358 (2020).

    Article 

    Google Scholar 

  • 60.

    Cascão, I., Domokos, R. K., Lammers, M. O., Santos, R. S. & Silva, M. N. A. Seamount effects on the diel vertical migration and spatial structure of micronekton. Prog. Ocean. 175, 1–13. https://doi.org/10.1016/j.pocean.2019.03.008 (2019).

    Article 

    Google Scholar 

  • 61.

    Fock, H., Matthiessen, B., Zidowitz, H. & Westernhagen, H. Diel and habitat-dependent resource utilisation of deep-sea fishes at the Great Meteor seamount (subtropical NE Atlantic): niche overlap and support for the sound-scattering layer-interception hypothesis. Mar. Ecol. Progr. Ser. 244, 219–233. https://doi.org/10.3354/meps244219 (2002).

    ADS 
    Article 

    Google Scholar 

  • 62.

    Laval, P. Hyperiid amphipods as crustacean parasitoids associated with gelatinous zooplankton. Oceanogr. Mar. Biol. Annu. Rev. 18, 11–56 (1980).

    Google Scholar 

  • 63.

    Madin, L. P. & Harbison, G. R. The associations of Amphipoda Hyperiidea with gelatinous zooplankton—I Associations with Salpidae. Deep-Sea Res. 24, 449–463. https://doi.org/10.1016/0146-6291(77)90483-0 (1977).

    ADS 
    Article 

    Google Scholar 

  • 64.

    Gasca, R., Hoover, R. & Haddock, S. H. D. New symbiotic associations of hyperiid amphipods (Peracarida) with gelatinous zooplankton in deep waters off California. J. Mar. Biol. Assoc. UK 95, 503–511. https://doi.org/10.1017/S0025315414001416 (2015).

    Article 

    Google Scholar 

  • 65.

    Harbison, G. R., Biggs, D. C. & Madin, L. P. The associations of Amphipoda Hyperiidea with gelatinous zooplankton—II. Associations with Cnidaria, Ctenophora and Radiolaria. Deep Sea Res. 24, 465–488. https://doi.org/10.1016/0146-6291(77)90484-2 (1977).

    ADS 
    Article 

    Google Scholar 

  • 66.

    Harbison, G. R., Madin, L. P. & Swanberg, N. R. On the natural history and distribution of oceanic ctenophores. Deep-Sea Res. 25, 233–256 (1978).

    ADS 
    Article 

    Google Scholar 

  • 67.

    Laval, P. The barrel of the pelagic amphipod Phronima sedentaria (Forsk.) (Crustacea: hyperiidea). J. Exp. Mar. Biol. Ecol. 33, 187–211. https://doi.org/10.1016/0022-0981(78)90008-4 (1978).

    Article 

    Google Scholar 

  • 68.

    Desmarest, A.-G. in Dictionnaire des Sciences Naturelles, 28. (ed F.G. Levrault) 138–425 (Paris and Strasbourg, 1823).

  • 69.

    Laval, P. Observations on biology of Phronima curvipes Voss (Amphipoda Hyperidae) and description of adult male. Cah. Biol. Mar. 9, 347–362 (1968).

    Google Scholar 

  • 70.

    Janssen, J. & Harbison, G. R. Fish in Salps: the Association of Squaretails (Tetragonurus Spp) with Pelagic Tunicates. J. Mar. Biol. Assoc. UK. 61, 917–927. https://doi.org/10.1017/S0025315400023055 (1981).

    Article 

    Google Scholar 

  • 71.

    Choy, C. A., Haddock, S. H. D. & Robison, B. H. Deep pelagic food web structure as revealed by in situ feeding observations. Proc. R. Soc. B Biol. Sci. 284, 20172116. https://doi.org/10.1098/rspb.2017.2116 (2017).

    Article 

    Google Scholar 

  • 72.

    Robison, B. H., Sherlock, R. E., Reisenbichler, K. R. & McGill, P. R. Running the gauntlet: assessing the threats to vertical migrators. Front. Mar. Sci. https://doi.org/10.3389/fmars.2020.00064 (2020).

    Article 

    Google Scholar 

  • 73.

    Hoving, H. J., Neitzel, P. & Robison, B. In situ observations lead to the discovery of the large ctenophore Kiyohimea usagi (Lobata: Eurhamphaeidae) in the eastern tropical Atlantic. Zootaxa 4526, 232–238. https://doi.org/10.11646/zootaxa.4526.2.8 (2018).

    Article 
    PubMed 

    Google Scholar 

  • 74.

    Arai, M. N. Predation on pelagic coelenterates: a review. J. Mar. Biol. Assoc. UK. 85, 523–536. https://doi.org/10.1017/S0025315405011458 (2005).

    Article 

    Google Scholar 


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