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Figure 9. A in Calcareous sponges of the genera Clathrina and Guancha (Calcinea, Calcarea, Porifera) of Norway (north-east Atlantic) with the description of five new species
Figure 9. A, Clathrina nanseni at 5 m depth. Scale bar = 1 cm. B, habitus of a fixed specimen. Scale bar = 1 cm. C, spicules of C. nanseni. tr = regular triactine. te = regular tetractine. Scale bar = 100 µm. D, tetractine with rudimentary and rounded apical actine. Scale bar = 100 µm. E, sharply pointed apical actine of a normal tetractine (ap). Scale bar = 100 µm. F, section of ascon tubes with the apical actines (ap) projecting into the interior of the tube. Scale bar = 100 µm.
Figure 1. A in Calcareous sponges of the genera Clathrina and Guancha (Calcinea, Calcarea, Porifera) of Norway (north-east Atlantic) with the description of five new species
Figure 1. A, holotype of Clathrina corallicola sp. nov. Scale bar = 1 cm. B, spicules of C. corallicola. lte = large tetractines, ste = small tetractines and str = small triactines. Scale bar = 200 µm. C, SEM photo of spicules of C. corallicola. ap = apical actine of sagittal tetractine. Scale bar = 200 µm. D, distribution of spicules seen from the atrial side of the tube wall. Note that the apical actines of the tetractines are orientated towards the interior of the tube. Scale bar = 200 µm.
Figure 5. A in Calcareous sponges of the genera Clathrina and Guancha (Calcinea, Calcarea, Porifera) of Norway (north-east Atlantic) with the description of five new species
Figure 5. A, Clathrina cribrata at 5 m depth. Scale bar = 1 cm. B, holotype of Clathrina cribrata. Note the many erect oscular tubes (arrow). Scale bar = 1 cm. C, regular triactines. Scale bar = 100 µm. D, transverse section of the osculum, showing the sieve of cells (cribrum). Scale bar = 100 µm.
Figure 5 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 5. Vigtorniella spp. Haplotype network of cytochrome c oxidase subunit I (COI). Each large circle represents a sequence from an individual of Vigtorniella ardabilia that has been collected in Sweden (white) or Norway (grey). Black circles represent V. flokati, collected in the Pacific Ocean, three specimens sampled sharing the same haplotype. Letters in circles, A-G, represent haplotypes of V. ardabilia sampled in this study (Table 1). Each line represents a mutation and small empty circles are inferred haplotypes not present in the current study.
Figure 4 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 4. Vigtorniella ardabilia sp. nov., specimen from whale-fall in Sweden, light micrographs: (A) parapodia from mid-body region, (B) detail of neuropodial falcigers, (C) detail of notopodial spine. Scale bar in (A) is 100 Mm, in (B) and (C) 10 Mm.
Figure 3 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 3. Vigtorniella ardabilia sp. nov., specimen from whale-fall in Sweden. SEM micrographs of (A) head region dorsal view, (B) head region ventral view, (C) fine neuropodial falcigers from segment 2, (D) neuropodial falcigers from mid-body region, and (E) notopodial spine. Scale bars in (A) and (B) are 150 Mm, in (C) 7.5 Mm, in (D) 15 Mm and in (E) 6 Mm.
Figure 2 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 2. Vigtorniella ardabilia sp. nov., live photo of specimen from whale-fall in Sweden. The worm is 6 mm long.
Figure 3 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 3. Relationship between the number of chaetigers and total bodylength in 15 specimens of Vigtorniella ardabilia and 33 specimens of V. flokati.
Figure 6. Diagram showing Kimura 2 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 6. Diagram showing Kimura 2 Parameter (K2P)-distances between congeneric species in four chrysopetalid genera, for two nuclear genes (18S, 28S) and two mitochondrial genes (16S, cytochrome c oxidase subunit I (COI)).
Figure 9 in Biogeography, phylogeny and acoustics of the flightless bush-crickets of the East African genus Monticolaria Sjöstedt, 1909, with the description of a new species (Orthoptera: Phaneropterinae)
Figure 9. Male stridulatory file of Monticolaria kilimandjarica (A–C), M. manyara (D–F) and M. meruensis (G–I). A,D,G, overview; B,E,H, details of the file near the wing base; C,F,I large stridulatory teeth (wing base to the right; see text).
Figure 11 in Biogeography, phylogeny and acoustics of the flightless bush-crickets of the East African genus Monticolaria Sjöstedt, 1909, with the description of a new species (Orthoptera: Phaneropterinae)
Figure 11. Distribution of Phaneropterinae taxa in montanous areas of East Africa morphologically related to Monticolaria.
Figure 7 in Biogeography, phylogeny and acoustics of the flightless bush-crickets of the East African genus Monticolaria Sjöstedt, 1909, with the description of a new species (Orthoptera: Phaneropterinae)
Figure 7. Spectrum of the song of Monticolaria kilimandjarica, high pass filtered at 4 kHz. Black line: song recorded with Genrad 1988 in the laboratory. Grey: song recorded with Pettersson D1000X in the field; peak at about 5–10 kHz from Aerotegmina kilimandjarica, at 40–45 kHz from Amytta olindo, both singing simultaneously.
Figure 6 in Biogeography, phylogeny and acoustics of the flightless bush-crickets of the East African genus Monticolaria Sjöstedt, 1909, with the description of a new species (Orthoptera: Phaneropterinae)
Figure 6. Song of Monticolaria kilimandjarica. A–F: calling song. A, field recording; B–F, laboratory recording; G, H, rivalry song? (see text).
Figure 4 in Biogeography, phylogeny and acoustics of the flightless bush-crickets of the East African genus Monticolaria Sjöstedt, 1909, with the description of a new species (Orthoptera: Phaneropterinae)
Figure 4. Lateral view on fastigium verticis of male: A, M. manyara; B, M. kilimandjaric; C, M. meruensis. Abdominal apices of male: D, M. manyara; E, M. kilimandjarica; and F, M. meruensis. Lateral view of abdominal apex of female: G, M. manyara; H, M. kilimandjarica; I, M. meruensis (scale bars represent 2 mm).
Figure 1 in Biogeography, phylogeny and acoustics of the flightless bush-crickets of the East African genus Monticolaria Sjöstedt, 1909, with the description of a new species (Orthoptera: Phaneropterinae)
Figure 1. Molecular phylogeny of Monticolaria species based on DNA sequences from the mitochondrial gene cytochrome oxidase subunit I (COI). Bootstrap values (1000 replicates) at nodes in the order: distance, ML, MP. '*' for nodes not resolved.
Figure 5. A, Male M in Biogeography, phylogeny and acoustics of the flightless bush-crickets of the East African genus Monticolaria Sjöstedt, 1909, with the description of a new species (Orthoptera: Phaneropterinae)
Figure 5. A, Male M. manyara; B, habitat of M. manyara: strongly disturbed montane forest on the southern slopes of Mt. Hanang; C, female M. kilimandjarica; D, male M. kilimandjarica.
Figure 16 in North-east Atlantic and Mediterranean species of the genus Buffonellaria (Bryozoa, Cheilostomata): implications for biodiversity and biogeography
Figure 16. Distribution of North Atlantic and Mediterranean Buffonellaria species. Note that the Greenland location of Buffonellaria arctica sp. nov. was randomly chosen, as these samples lack specific locality information.
Figure 15 in North-east Atlantic and Mediterranean species of the genus Buffonellaria (Bryozoa, Cheilostomata): implications for biodiversity and biogeography
Figure 15. Buffonellaria sp. 2: SMF 3015, off Sierra Leone. A, general aspect; scale bar, 200 Mm. B, Close-up of autozooecia; scale bar, 100 Mm.
Figure 13 in North-east Atlantic and Mediterranean species of the genus Buffonellaria (Bryozoa, Cheilostomata): implications for biodiversity and biogeography
Figure 13. Escharella linearis (Hassall, 1841) forma biaperta (Michelin, 1848): SNHM 1742, Svalbard, Edge Island, illustrated by Smitt (1868: pl. 24, figs 71–73), uncleaned specimen. A, autozooids at colony margin; note the large areolar pores compared with Buffonellaria arctica sp. nov.; scale bar, 400 Mm. B, autozooids with thick secondary calcification; scale bar, 200 Mm.
Figure 14 in North-east Atlantic and Mediterranean species of the genus Buffonellaria (Bryozoa, Cheilostomata): implications for biodiversity and biogeography
Figure 14. Buffonellaria porcellanum Arístegui Ruiz, 1987: holotype, NHM 1987.1.3.2, Canary Islands. A, general aspect; note the reparative growth in zooecia on the right, and the reversed polarity growth of two zooecia at the centre; scale bar, 200 Mm. B, autozooecia and ovicellate zooecia; scale bar, 100 Mm. C, close-up of orifice; scale bar, 50 Mm. D, close-up of ooecium; scale bar, 40 Mm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.