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340 results for “marine diversity”
Genetic diversity of a marine foundation species, Laminaria hyperborea (Phaeophyceae Laminariales), along the coast of Ireland
<p><span><span><span><span><span><span><span><span><span><span><span>Worldwide, kelp populations are stressed by warming, increased storms and other man-driven disturbances<i>. </i>Marine population distributions are projected to retreat poleward with climate change if they cannot adapt to changing conditions, which would potentially lead to a regime shift in subtidal habitats. In Northern Europe, <i>Laminaria hyperborea</i>is a subtidal ecosystem engineer whose distribution has shifted over millennia, leaving predicted areas of high genetic diversity from the last glacial maximum (LGM) near its southern distribution limit in the Iberian Peninsula. In Ireland, <i>L. hyperborea </i>structures communities by supporting diverse faunal assemblages and producing large quantities of organic carbon throughout the year. We investigated the genetic diversity of eight populations ranging from the southern coast to the northwest of Ireland using nine microsatellite loci. Diversity was found to be highest in Lough Hyne, a Special Area of Conservation (SAC), near the predicted climate refugium. We found evidence of isolation by distance, with high connectivity between populations that were geographically close, likely driven by short range dispersal of <i>L. hyperborea</i>propagules. Genetic diversity (measured as expected heterozygosity and allelic richness) was highest at Lough Hyne, and decreased northwards, as predicted from past range shifts. Expected heterozygosity was highest at Lough Hyne (0.706) and decreased northward, with the lowest value at Bridges of Ross (0.283). Based on these patterns, further fine-scale investigation into population diversity, dispersal and potential resilience in Irish kelp forests are necessary as warming and non-native species are observed more and more frequently.</span></span></span></span></span></span></span></span></span></span></span></p>
FIG. 1 in Marine cyanobacteria diversity and biotechnological potential in Caribbean waters
FIG. 1. — Map showing Caribbean countries were studies on cyanobacteria have been reported (gray) and those that have no reports yet (white).
Fig. 2A–H in Dirty Tricks in the Plankton: Diversity and Role of Marine Parasitic Protists
Fig. 2A–H. Protistan parasites of marine zooplankton. A – the dinoflagellate Haplozoon inerme (bottom left) parasitizing Appendicularia sicula (after Cachon 1964); B, C – hyperparasitic Amobophrya grassi in Oodinium poucheti, an ectoparasites on Oikopleura (after Cachon 1964); B – several early-stage parasites inside the host; C – macrospore (left) and dividing microspores (right) of A. grassi; D, E – the syndinean dinoflagellate Syndinium bogerti in the acantharian Amphilonche sp. (after Hollande and Enjumet 1955); D – multinuclear parasites inside the host; E – relased parasite macrospore (left) and microspore (right); F–H – Syndinium- like parasite in the copepod Clausocalanus sp. from the NW Mediterranean Sea; F, G – dinospores originating from the infected host in H. Scale bars: 10 µm; H – recently diseased host filled with live dinospores. Scale bar: 100 µm.
Fig. 1A in Dirty Tricks in the Plankton: Diversity and Role of Marine Parasitic Protists
Fig. 1A–-E. Protistan parasites of marine phytoplankton. A – Amoeba biddulphiae in the diatom Odontella sinensis. Left: recently attached parasite cell. Center: parasitic amoeba inside the host. Rigth: almost empty diatom frustule with protoplasm transformed into 10 amoebae (after Zuelzer 1927); B, C – the stramenopile fungi Lagenisma coscinodisci in the diatom Coscinodiscus sp.; B – host cell protoplasm transformed into parasite hyphae; C – expulsion of parasite swarmer cells. Courtesy of Gerhard Drebes, Plankton*Net Data Provider at the Alfred Wegener Institute for Polar and Marine, http://planktonnet. awi.de; D – Parvilucifera sp. sporangium in a deceased dinoflagellate, Tripos macroceros, from the North Sea; E – Amoebophrya sp. in the dinoflagellate Tripos fusus from the North Sea. Arrows show extreme points of parasite. All scale bars: 50 µm.
Fig. 20 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 20. Relative abundance of lecithotrophic y-nauplii at Sesoko Island (Okinawa, Japan) during field work in 2018 and 2019. Grey bars denote the number of lecithotrophic nauplii of each morphospecies that survived until the last naupliar stage during laboratory rearing. Blue bars show the numbers of cyprids that successfully molted from these last-stage nauplii. Images of all lecithotrophic y-naupliar morphospecies obtained during those two years are shown to the same scale.
Fig. 19 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 19. Last-stage nauplii of four different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–E. Y-nauplius Type AK. F–G. Y-nauplius Type AO. H. Y-nauplius Type AM. I–K. Y-nauplius Type AN. Shown either in life (A–B, H) or as slide-mounted exuviae (C–G, I–K). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 16 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 16. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–E. Y-nauplius Type Y. F–J. Y-nauplius Type O*. Shown either in life (A, F–G) or as slide-mounted exuviae (B–E, H–J). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 18 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 18. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–F. Y-nauplius Type AL. G–J. Y-nauplius Type AJ. Shown either in life (A–C, G–J) or as slide-mounted exuviae (D–F). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 17 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 17. Last-stage nauplii of three different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–E. Y-nauplius Type AF. F–K. Y-nauplius Type N*. L. Y-nauplius Type AP. Shown either in life (A–C, F–G) or as slide-mounted exuviae (D–E, H–L). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible. L from Grygier et al. (2019).
Fig. 15 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 15. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–F. Y-nauplius Type L. G–M. Y-nauplius Type AB. Shown either in life (A–C, G–J) or as slide-mounted exuviae (D–F, K–M). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 13 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 13. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–E. Y-nauplius Type X. F–J. Y-nauplius Type K. Shown either in life (A–B, F–H) or as slide-mounted exuviae (C–E, I–J). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 14 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 14. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–F. Y-nauplius Type M. G–L. Y-nauplius Type AI. Shown either in life (A–B, G–I) or as slide-mounted exuviae (C–F, J–L). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 9 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 9. Last-stage nauplii of four different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–C. Hansenocaris cristalabri Olesen & Grygier, 2022. D–E. Hansenocaris aquila Olesen & Grygier, 2022. F–H. Y-nauplius Type AC. I–N. Y-nauplius Type AH*. Shown either in life (A–B, F–H, I–J), as slide-mounted exuviae (D–E, K–N) or in SEM (C). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible. A–E from Olesen & Grygier (2022).
Fig. 4 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 4. Planktotrophic (feeding) y-nauplius of morphospecies Type A*. A. Ventral view. B. Lateral view. C. Naupliar feeding apparatus of right side. D. Postero-lateral spines of left side, dorso-caudal organ, dorso-caudal spine and furcal spines. The naupliar feeding apparatus, postero-lateral spines, dorsocaudal organ and dorso-ventrally flattened body (especially the first of these) are the key characters for separating planktotrophic y-nauplii from lecithotrophic y-nauplii. Abbreviations: Bas = basis; Cox = coxa; En = endopod; 1–3 = postero-lateral spine rows on trunk.
Fig. 11 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 11. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–G. Y-nauplius Type W. H–M. Y-nauplius Type AD. Shown either in life (A–C, H–J) or as slide-mounted exuviae (D–G, K–M). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 8 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 8. Last-stage nauplii of three different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–D. Type F. E–G. Type G. H–J. Type H. Shown either in life (A–B, E–F, H–I) or as slide-mounted exuviae (C–D, G, J). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 10 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 10. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–F. Y-nauplius Type E*. G–K. Y-nauplius Type AG*. Shown either in life (A–B, G–H) or as slide-mounted exuviae (C–F, I–K). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 3 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 3. Example of canvasses used to sort images of more than 500 last-stage y-nauplii obtained during field work at Sesoko Island (Okinawa, Japan) in 2018 and 2019 into morphospecies. This canvas shows different developmental stages of 52 specimens of a particularly distinctive morphospecies, Type C (nicknamed 'Bumblebee' due to its distinct color pattern), with color codes indicating each specimen's manner of preservation and storage.
Fig. 7 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 7. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–G. Type D* ("Big brown"). H–M. Type B. Shown either in life (A–B, H–J) or as slide-mounted exuviae (C–G, K–M). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 2. Y in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 2. Y-naupliar (Facetotecta) diversity at Sesoko Island (Okinawa, Japan). A. Schematic life cycle of y-larvae (modified from Itô 1991; Glenner et al. 2008). B. Overview of 34 morphospecies of lecithotrophic last-stage y-nauplii obtained by laboratory rearing of earlier-stage nauplii collected in the plankton; three of them represent formally described species while 31 remain undescribed. C. Nine types of planktotrophic y-larvae, of which only Type A* is treated in detail in this paper. All photos in B and C are to the same scale. Figure also used in Olesen (2004). Examples of live video of most of the y-naupliar morphospecies can be seen at https://youtu.be/er0mYLswV-c and are also deposited at Figshare.com: https://doi.org/10.6084/m9.figshare.24953568.v1.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.