Gelatinous zooplankton

Source: Wikipedia, the free encyclopedia.
Jellyfish are easy to capture and digest and may be more important as food sources than was previously thought.[1]

Gelatinous zooplankton are fragile animals that live in the

Arthropoda, contain gelatinous species, but many of those odd species live in the open ocean and the deep sea and are less available to the casual ocean observer.[4] Many gelatinous plankters utilize mucous structures in order to filter feed.[5] Gelatinous zooplankton have also been called Gelata.[6]

As prey

Jellyfish are slow swimmers, and most species form part of the plankton. Traditionally jellyfish have been viewed as trophic dead ends, minor players in the marine food web, gelatinous organisms with a

amphipods.[8][1] "Despite their low energy density, the contribution of jellyfish to the energy budgets of predators may be much greater than assumed because of rapid digestion, low capture costs, availability, and selective feeding on the more energy-rich components. Feeding on jellyfish may make marine predators susceptible to ingestion of plastics."[1]

As predators

According to a 2017 study,

ctenophores and cephalopods.[9] The importance of the so-called "jelly web" is only beginning to be understood, but it seems medusae, ctenophores and siphonophores can be key predators in deep pelagic food webs with ecological impacts similar to predator fish and squid. Traditionally gelatinous predators were thought ineffectual providers of marine trophic pathways, but they appear to have substantial and integral roles in deep pelagic food webs.[9]

Pelagic

Portuguese man of war, to the deep sea. They play important roles in ocean ecosystems, and are among the most abundant gelatinous predators.[10]

  • Helmet jellyfish feeding on an armhook squid
    armhook squid
  • Trachymedusa with a large red mysid in its gut
    mysid
    in its gut

Jelly pump

Longhurst Provinces modelled.[11]

Biological oceanic processes, primarily carbon production in the

remineralization, govern the global biological carbon soft‐tissue pump.[12] Sinking and laterally transported carbon‐laden particles fuel benthic ecosystems at continental margins and in the deep sea.[13][14] Marine zooplankton play a major role as ecosystem engineers in coastal and open ocean ecosystems because they serve as links between primary production, higher trophic levels, and deep‐sea communities.[15][14][16] In particular, gelatinous zooplankton (Cnidaria, Ctenophora, and Chordata, namely, Thaliacea) are universal members of plankton communities that graze on phytoplankton and prey on other zooplankton and ichthyoplankton. They also can rapidly reproduce on a time scale of days and, under favorable environmental conditions, some species form dense blooms that extend for many square kilometers.[17] These blooms have negative ecological and socioeconomic impacts by reducing commercially harvested fish species,[18] limiting carbon transfer to other trophic levels,[19] enhancing microbial remineralization, and thereby driving oxygen concentrations down close to anoxic levels.[20][11]

Gelatinous zooplankton biological pump
How jelly carbon fits in the biological pump. A schematic representation of the biological pump and the biogeochemical processes that remove elements from the surface ocean by sinking biogenic particles including jelly carbon.[11]

Jelly carbon

The global biomass of gelatinous zooplankton (sometimes referred to as jelly‐C) within the upper 200 m of the ocean amounts to 0.038

biogeographical provinces that partition the pelagic environment,[28][29] the highest densities of gelatinous zooplankton occur in coastal waters of the Humboldt Current, NE U.S. Shelf, Scotian and Newfoundland shelves, Benguela Current, East China and Yellow Seas, followed by polar regions of the East Bering and Okhotsk Seas, the Southern Ocean, enclosed bodies of water such as the Black Sea and the Mediterranean, and the west Pacific waters of the Japan seas and the Kuroshio Current.[30][31][21] Large amounts of jelly carbon biomass that are reported from coastal areas of open shelves and semi-enclosed seas of North America, Europe, and East Asia come from coastal stranding data.[32][11]

Carbon export

Large amounts of jelly carbon are quickly transferred to and remineralized on the seabed in coastal areas, including estuaries, lagoons and subtidal/intertidal zones,

macrofauna and megafauna once on the seabed.[41][42] Despite the high lability of jelly‐C,[43][39] a remarkably large amount of biomass arrives at the seabed below 1,000 m. During sinking, jelly‐C biochemical composition changes via shifts in C:N:P ratios as observed in experimental studies.[20][44][45] Yet realistic jelly‐C transfer estimates at the global scale remain in their infancy, preventing a quantitative assessment of the contribution to the biological carbon soft‐tissue pump.[11]

continental shelves. Thaliaceans play an important role in the ecology of the sea. Their dense faecal pellets sink to the bottom of the oceans and this may be a major part of the worldwide carbon cycle.[46]

Ocean carbon export is typically estimated from the flux of sinking particles that are either caught in sediment traps [47] or quantified from videography,[48] and subsequently modeled using sinking rates.[49] Biogeochemical models [50][51][52] are normally parameterized using particulate organic matter data (e.g., 0.5–1,000 μm marine snow and fecal pellets) that were derived from laboratory experiments [53] or from sediment trap data.[50] These models do not include jelly‐C (except larvaceans,[54][55] not only because this carbon transport mechanism is considered transient/episodic and not usually observed, and mass fluxes are too big to be collected by sediment traps,[27] but also because models aim to simplify the biotic compartments to facilitate calculations. Furthermore, jelly‐C deposits tend not to build up at the seafloor over a long time, such as phytodetritus (Beaulieu, 2002), being consumed rapidly by demersal and benthic organisms [41] or decomposed by microbes.[42] The jelly‐C sinking rate is governed by organism size, diameter, biovolume, geometry,[56] density,[57] and drag coefficients.[58] In 2013, Lebrato et al. determined the average sinking speed of jelly‐C using Cnidaria, Ctenophora, and Thaliacea samples, which ranged from 800 to 1,500 m day−1 (salps: 800–1,200 m day−1; scyphozoans: 1,000–1,100 m d−1; ctenophores: 1,200–1,500 m day−1; pyrosomes: 1,300 m day−1).[59] Jelly‐C model simulations suggest that, regardless of taxa, higher latitudes are more efficient corridors to transfer jelly‐C to the seabed owing to lower remineralization rates.[60] In subtropical and temperate regions, significant decomposition takes place in the water column above 1,500 m depth, except in cases where jelly‐C starts sinking below the thermocline. In shallow‐water coastal regions, time is a limiting factor, which prevents remineralization while sinking and results in the accumulation of decomposing jelly‐C from a variety of taxa on the seabed. This suggests that gelatinous zooplankton transfer most biomass and carbon to the deep ocean, enhancing coastal carbon fluxes via DOC and DIC, fueling microbial and megafaunal/macrofaunal scavenging communities. However, the absence of satellite‐derived jelly‐C measurements (such as primary production) [61] and the limited number of global zooplankton biomass data sets make it challenging to quantify global jelly‐C production and transfer efficiency to the ocean's interior.[11]

Monitoring

Because of its fragile structure, image acquisition of gelatinous zooplankton requires the assistance of

Tikhonov regularization, support vector machines and genetic programming.[62]

The Beroe ctenophore, mouth gaping, preys on other ctenophores

See also

  • Sea snot

References

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  4. ^ Nouvian, C. (2007) The Deep. University of Chicago Press.
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  6. ^ HADDOCK, S.D.H. (2004) A golden age of gelata: past and future research on planktonic ctenophores and cnidarians. Hydrobiologia 530/531: 549–556.
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  12. ^ Koppelmann, R., & Frost, J. (2008). "The ecological role of zooplankton in the twilight and dark zones of the ocean". In: L. P. Mertens (Ed.), Biological Oceanography Research Trends, pages 67–130. New York: Nova Science Publishers.
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