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Figure 9 in A revision of West Palaearctic species of the Micropsectra atrofasciata species group (Diptera: Chironomidae)
Figure 9. Micropsectra calcifontis sp. nov. A, hypopygium. B, anal point, lateral view. C, median volsella. D, superior, median and inferior volsellae.
Figure 6 in Towards a revision of the genus Parastenocaris Kessler, 1913: establishment of Simplicaris gen. nov. from groundwaters in central Italy and review of the P. brevipes-group (Copepoda, Harpacticoida, Parastenocarididae)
Figure 6. Genital field in A, Simplicaris lethaea gen. et sp. nov. (♀). B, Parastenocaris brevipes (♀), Onkimanjarvi Lake, Finland (USNM 259764). Arrow indicates the copulatory pore.
Figure 5. Male P4 in Towards a revision of the genus Parastenocaris Kessler, 1913: establishment of Simplicaris gen. nov. from groundwaters in central Italy and review of the P. brevipes-group (Copepoda, Harpacticoida, Parastenocarididae)
Figure 5. Male P4 exopod in representative members of the family Parastenocarididae. A, Simplicaris lethaea gen. et sp. nov. B, Parastenocaris brevipes, Onkimanjarvi Lake, Finland (USNM 259764). C, Parastenocaris glareola Hertzog, 1936, River Rhône, France.
Figure 4 in Towards a revision of the genus Parastenocaris Kessler, 1913: establishment of Simplicaris gen. nov. from groundwaters in central Italy and review of the P. brevipes-group (Copepoda, Harpacticoida, Parastenocarididae)
Figure 4. Segmental pattern of male antennule in representative members of Parastenocarididae. A, Simplicaris lethaea gen. et sp. nov. (♂). B, Parastenocaris brevipes Kessler, 1913 (♂), Onkimanjarvi Lake, Finland (USNM 259764). C, Forficatocaris claudii (♂) (after Ahnert, 1994; redrawn).
Figure 2 in Towards a revision of the genus Parastenocaris Kessler, 1913: establishment of Simplicaris gen. nov. from groundwaters in central Italy and review of the P. brevipes-group (Copepoda, Harpacticoida, Parastenocarididae)
Figure 2. Simplicaris lethaea gen. et sp. nov. (A-C, G: ♂ paratype; D-F, H: ♂ holotype). A, mandible. B, maxillule. C, maxilla. D, maxilliped. E, P1. F, P2. G, P3. H, P4.
Figure 3 in Towards a revision of the genus Parastenocaris Kessler, 1913: establishment of Simplicaris gen. nov. from groundwaters in central Italy and review of the P. brevipes-group (Copepoda, Harpacticoida, Parastenocarididae)
Figure 3. Simplicaris lethaea gen. et sp. nov. (♀ paratype). A, urosome. B, genital field. C, antennule. D, P2. E, P3. F, P4.
Figure 1 in Towards a revision of the genus Parastenocaris Kessler, 1913: establishment of Simplicaris gen. nov. from groundwaters in central Italy and review of the P. brevipes-group (Copepoda, Harpacticoida, Parastenocarididae)
Figure 1. Simplicaris lethaea gen. et sp. nov. (A, C: ♂ paratype; B, D: ♂ holotype). A, habitus. B, urosome. C, antennule. D, antenna.
Figure 14 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 14. Internal mould of Paracyclas proavia (Goldfuss, 1840) from the Devonian, Eifel, Germany (BMNH Pal. Department L25554). Shell length = 56 mm. A, right side, anterior adductor scar arrowed; B, detail of anterior adductor scar showing ventral detachment from pallial line. aas, anterior adductor muscle scar; pl, pallial line.
Figure 13. A, B in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 13. A, B, internal moulds showing right sides of Ilionia prisca, Silurian, Gotland, Sweden. A, BMNH, Shell length (SL) = 70 mm; B, BMNH, SL = 55 mm. C, D, outside and inside of left valve of Eomiltha voorhoevi, Recent, Mozambique, ANSP 234103, SL = 70 mm.
Figure 12 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 12. Posterior apertures of Fimbria fimbriata (Lizard Island, Queensland) showing double row of papillae, and short length of mantle fusion ventral to inhalant aperture. Abbreviations: ex, exhalant aperture; in, inhalant aperture; pg, pedal gape; vf, ventral fusion.
Figure 11 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 11. Posterior apertures of a range of lucinid species. All SEMs of critical point dried specimens. A, Anodontia omissa (Iredale, 1930), Moreton Bay Queensland; B, Phacoides pectinatus (Gmelin, 1792), Brazil; C, Bathyaustriella thionipta (Glover et al., 2004), Kermadec Ridge, New Zealand; D, Ctena bella (Conrad, 1837), Lizard Island, Queensland; E, Pillucina vietnamica Zorina, 1978, Port Douglas, Queensland; F, Wallucina assimilis (Angas, 1867), Jervis Bay, New South Wales; G, Lucina adansoni d'Orbigny, 1839, Cape Verde Islands. H, Cardiolucina pisiformis (Thiele, 1930), Shark Bay, Western Australia; I, Myrtea spinifera (Montagu, 1803), Oban Scotland. Images adjusted to similar scale. Abbreviations: ex, exhalant aperture; in, inhalant aperture; p, papillae; vf, ventral mantle fusion.
Figure 9 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 9. SEM section of ctenidial filament of Lucinisca nassula (Conrad, 1846) showing bacteriocytes and granule cells. Scale bar = 10 µm. Abbreviations b, bacteriocyte with rod-shaped bacteria. gr, granule cell and granules.
Figure 8 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 8. TEM section through part of ctenidial filament of Anodontia ovum (Reeve, 1850), Lizard Island, Queensland, showing central blood space flanked by bacteriocytes and intercalary cells. Scale bar = 5 µm. Abbreviations: b, bacteria; ba, bacteriocyte; bs, blood space; eic, distal extension of intercalary cell; ic, intercalary cell; ly, lysosome; m, microvilli; n, nucleus.
Figure 7 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 7. Composite tree of lucinid relationships derived from Bretsky (1976: figs 3–9) and including living taxa only.
Figure 10 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 10. Mantle gills in lucinids. A, Codakia tigerina; B, Lucina pensylvanica; C, Phacoides pectinatus; D, Anodontia philippiana. Scale bars = 1 mm.
Figure 6 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 6. Tree summarizing Chavan's (1969) ideas of relationships in Lucinidae derived from his subfamilial classification of genera. Recent taxa only included.
Figure 1 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 1. Diversity of form within Lucinidae. A, Plicolucina flabellata Glover, Taylor & Slack-Smith, 2003, Shell length (SL) = 22 mm; B, Lamellolucina trisulcata Taylor & Glover, 2002, SL = 10 mm; C, Codakia tigerina (Linnaeus, 1758), SL = 70 mm; D, Anodontia philippiana (Reeve, 1850), SL = 66 mm; E, Miltha childrenae (Gray 1825), SL = 82 mm; F, Eomiltha voorhoevi, SL = 80 mm; G, Austriella corrugata (Deshayes, 1843), SL = 60 mm; H, Ctena bella (Conrad, 1837), SL = 25 mm; I, Rasta lamyi (Abrard, 1942), SL = 30 mm; J, Pompholigina gibba (Gray, 1825), SL = 27 mm; K, Myrtea spinifera (Montagu, 1803), SL = 26 mm.
Figure 5 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 5. Tree of lucinid relationships derived from final figure (tableau chronologique de l'evolution des lucines) by Chavan, 1937−1938), including living taxa only.
Figure 4 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 4. General anatomy of Anodontia philippiana, Dampier, Western Australia, with left valve and mantle removed. Abbreviations: aa, anterior adductor muscle; exa, exhalant aperture; f, foot; fm, fused mantle; ld, left demibranch of ctenidia; me, mantle edge; mg, mantle gills on septum; p, periostracum; pa, posterior adductor muscle. Shell length = 40 mm
Figure 2 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs
Figure 2. Molecular phylogeny of heterodont and palaeoheterodont bivalves produced by Bayesian analysis of partial sequences from the 18SrRNA gene. Branches with posterior probabilities <85% have been collapsed. Nodal support is posterior probability/bootstrap (Neighbour-joining using Maximum Likelihood distance, 10 000 reps). Details of taxa and methods in Taylor et al., 2005.
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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)
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.