Characterization of species diversity of zooplankton is key to understanding, assessing, and predicting the function and future of pelagic ecosystems throughout the global ocean. The marine zooplankton assemblage, including only metazoans, is highly diverse and taxonomically complex, with an estimated ~28,000 species of 41 major taxonomic groups. This review provides a comprehensive summary of DNA sequences for the barcode region of mitochondrial cytochrome oxidase I (COI) for identified specimens. The foundation of this summary is the MetaZooGene Barcode Atlas and Database (MZGdb), a new open-access data and metadata portal that is linked to NCBI GenBank and BOLD data repositories. The MZGdb provides enhanced quality control and tools for assembling COI reference sequence databases that are specific to selected taxonomic groups and/or ocean regions, with associated metadata (e.g., collection georeferencing, verification of species identification, molecular protocols), and tools for statistical analysis, mapping, and visualization. To date, over 150,000 COI sequences for ~ 5600 described species of marine metazoan plankton (including holo- and meroplankton) are available via the MZGdb portal. This review uses the MZGdb as a resource for summaries of COI barcode data and metadata for important taxonomic groups of marine zooplankton and selected regions, including the North Atlantic, Arctic, North Pacific, and Southern Oceans. The MZGdb is designed to provide a foundation for analysis of species diversity of marine zooplankton based on DNA barcoding and metabarcoding for assessment of marine ecosystems and rapid detection of the impacts of climate change.
Aim Invasive species are of increasing global concern. Nevertheless, the mechanisms driving further distribution after the initial establishment of non‐native species remain largely unresolved, especially in marine systems. Ocean currents can be a major driver governing range occupancy, but this has not been accounted for in most invasion ecology studies so far. We investigate how well initial establishment areas are interconnected to later occupancy regions to test for the potential role of ocean currents driving secondary spread dynamics in order to infer invasion corridors and the source–sink dynamics of a non‐native holoplanktonic biological probe species on a continental scale. Location Western Eurasia. Time period 1980s–2016. Major taxa studied ‘Comb jelly’ Mnemiopsis leidyi. Methods Based on 12,400 geo‐referenced occurrence data, we reconstruct the invasion history of M. leidyi in western Eurasia. We model ocean currents and calculate their stability to match the temporal and spatial spread dynamics with large‐scale connectivity patterns via ocean currents. Additionally, genetic markers are used to test the predicted connectivity between subpopulations. Results Ocean currents can explain secondary spread dynamics, matching observed range expansions and the timing of first occurrence of our holoplanktonic non‐native biological probe species, leading to invasion corridors in western Eurasia. In northern Europe, regional extinctions after cold winters were followed by rapid recolonizations at a speed of up to 2,000 km per season. Source areas hosting year‐round populations in highly interconnected regions can re‐seed genotypes over large distances after local extinctions. Main conclusions Although the release of ballast water from container ships may contribute to the dispersal of non‐native species, our results highlight the importance of ocean currents driving secondary spread dynamics. Highly interconnected areas hosting invasive species are crucial for secondary spread dynamics on a continental scale. Invasion risk assessments should consider large‐scale connectivity patterns and the potential source regions of non‐native marine species.
Stemmann, L., Youngbluth, M., Robert, K., Hosia, A., Picheral, M., Paterson, H., Ibanez, F., Guidi, L., Lombard, F., and Gorsky, G. 2008. Global zoogeography of fragile macrozooplankton in the upper 100–1000 m inferred from the underwater video profiler. – ICES Journal of Marine Science, 65: 433–442. Mesopelagic gelatinous zooplankton fauna are insufficiently known because of inappropriate and infrequent sampling, but may have important trophic roles. In situ imaging systems and undersea vehicles have been used to investigate their diversity, distribution, and abundance. The use of different platforms, however, restricts the comparison of data from different regions. Starting in 2001, the underwater video profiler (UVP) was deployed during 12 cruises in six oceanic regimes (Mediterranean Sea, North Atlantic shelves, Mid-Atlantic Ridge, tropical Pacific Ocean, eastern Indian Ocean, and Subantarctic Ocean) to determine the vertical distribution of organisms in the upper 1000 m. Nine oceanic regions were identified based on the hydrological properties of the water column. They correspond to nine of the biogeochemical provinces defined by Longhurst. In all, 21 morphotypes were recognized: sarcodines (eight groups), ctenophores (two groups), siphonophores, medusae (five groups), crustaceans (one group), chaetognaths, appendicularians, salps, and fish. The similarity in the community assemblages of zooplankton in the 100–1000 m layer was significantly greater within regions than between regions, in most cases. The regions with comparable composition were located in the North Atlantic with adjacent water masses, suggesting that the assemblages were either mixed by advective transport or that environmental conditions were similar in mesopelagic layers. The data suggest that the spatial structuring of mesopelagic macrozooplankton occurs on large scales (e.g. basin scales) but not necessarily on smaller scales (e.g. oceanic front).
Quantitative seasonal studies on gelatinous zooplankton in Norwegian fjords are scarce. We recorded the quantitative composition of the gelatinous zooplankton community in Korsfjord and Fanafjord during 1 yr. Thirty-six species or genera of hydromedusae, 7 species of siphonophores, 4 species of ctenophores and 2 species of scyphomedusae were recorded. Aglantha digitale was numerically dominant in both fjords. A separate video-profiling study on the vertical distribution of fully grown specimens of this species was made in Korsfjord and the adjacent Bjørnafjord. Our data suggest 2 A. digitale generations yr -1 , with relatively low importance of the latter generation. The overwintering strategy includes autumn growth to full size and distribution at intermediate depth, mainly between 200 and 300 m. Siphonophores were prominent in the more oceanic Korsfjord, while Fanafjord was characterized by meroplanktonic hydromedusae. More species were recorded from Korsfjord, which may be partly attributed to the larger volume sampled and the higher probability of encountering oceanic visitors in this fjord. Korsfjord also harbored a community of deep-water hydromedusae absent from Fanafjord. The gelatinous community of both fjords was most numerous and species-rich from April to June. Spring maximum densities were higher in Fanafjord. During winter, gelatinous zooplankton was more abundant in Korsfjord, with eudoxids of Dimophyes arctica and Lensia conoidea forming the bulk of the community. Hydromedusa species appeared sequentially and differed in terms of maximum abundance attained and length of their presence in the plankton. Multivariate analyses revealed a clear seasonal succession for the gelatinous community of both fjords.
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