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Figure 2 from: Bragança PHN, van Zeeventer RM, Bills R, Tweddle D, Chakona A (2020) Diversity of the southern Africa Lacustricola Myers, 1924 and redescription of Lacustricola johnstoni (Günther, 1894) and Lacustricola myaposae (Boulenger, 1908) (Cyprinodontiformes, Procatopodidae). ZooKeys 923: 91-113. https://doi.org/10.3897/zookeys.923.48420
Figure 2 Southern Africa "Lacustricola" distribution maps. Spots correspond to the exact localities for the haplotypes included in this study, and the shaded area refers to the inferred distribution for each species. Map A yellow – "Lacustricola" hutereaui; grey – "L." johnstoni; brown – "L." myaposae; and purple – "L." jubbi. Map B dark green – "L." macrurus; orange – "L." mediolateralis; red – "L." katangae; light blue – "L." centralis; blue – "L. " aff. johnstoni 'Okavango'; light green – "L. " aff. johnstoni 'Congo'.
Figure 1 from: Bragança PHN, van Zeeventer RM, Bills R, Tweddle D, Chakona A (2020) Diversity of the southern Africa Lacustricola Myers, 1924 and redescription of Lacustricola johnstoni (Günther, 1894) and Lacustricola myaposae (Boulenger, 1908) (Cyprinodontiformes, Procatopodidae). ZooKeys 923: 91-113. https://doi.org/10.3897/zookeys.923.48420
Figure 1 Phylogenetic relationships between southern Africa "Lacustricola" haplotypes, based on COI mitochondrial DNA sequences. Numbers left to the bar indicate posterior probability values and on the right are bootstrap support values from the maximum likelihood analysis. Asterisks indicate maximum values. Colours next to each species name correspond to the same colours as depicted in the distribution map (Figure 2). Abbreviations refer to the country where the specimens were collected: ANG = Angola, BOT = Botswana, BUR = Burundi, DRC = Democratic Republic of Congo, NAM = Namibia, MAL = Malawi, MOZ = Mozambique, RSA = Republic of South Africa, ZAM = Zambia.
Figure 4 from: He X, Hsu WH, Hou R, Yao Y, Xu Q, Jiang D, Wang L, Wang H (2020) Comparative genomics reveals bamboo feeding adaptability in the giant panda (Ailuropoda melanoleuca). ZooKeys 923: 141-156. https://doi.org/10.3897/zookeys.923.39665
Figure 4 The GO enrichment analysis of giant panda positive selection gene. The abscissa is the pair value of the corrected p value, and the corrected p < 0.05 is taken as the threshold value.
Figure 3 from: He X, Hsu WH, Hou R, Yao Y, Xu Q, Jiang D, Wang L, Wang H (2020) Comparative genomics reveals bamboo feeding adaptability in the giant panda (Ailuropoda melanoleuca). ZooKeys 923: 141-156. https://doi.org/10.3897/zookeys.923.39665
Figure 3 The KEGG enrichment analysis of the giant panda expansion gene family. The abscissa is the pair value of the corrected p value, and the corrected p < 0.05 is taken as the threshold value.
Figure 2 from: He X, Hsu WH, Hou R, Yao Y, Xu Q, Jiang D, Wang L, Wang H (2020) Comparative genomics reveals bamboo feeding adaptability in the giant panda (Ailuropoda melanoleuca). ZooKeys 923: 141-156. https://doi.org/10.3897/zookeys.923.39665
Figure 2 Analysis of the evolution of giant panda gene family. The number of points represent the time of divergence, in millions of years (Myr). The numbers on the branches represent the number of genes, - for contraction, + for expansion.
Figure 1 from: He X, Hsu WH, Hou R, Yao Y, Xu Q, Jiang D, Wang L, Wang H (2020) Comparative genomics reveals bamboo feeding adaptability in the giant panda (Ailuropoda melanoleuca). ZooKeys 923: 141-156. https://doi.org/10.3897/zookeys.923.39665
Figure 1 The enrichment analysis of shared genes between the giant panda and mammalian species with different feeding habits. Giant pandas have the characteristics of both carnivores and herbivores. Studies show that it is close to carnivores in perception and close to herbivores in physiological functions. The abscissa is the pair value of the corrected p value, and the corrected p < 0.05 is taken as the threshold value. a shared genes between the giant panda and other mammalian species with different feeding habits b gene enrichment analysis of the giant panda and carnivores c gene enrichment analysis of the giant panda and herbivores.
Figure 1 from: Samuel S, Shadaydeh M, Böcker S, Brügmann B, Bucher SF, Deckert V, Denzler J, Dittrich P, von Eggeling F, Güllmar D, Guntinas-Lichius O, König-Ries B, Löffler F, Maicher L, Marz M, Migliavacca M, R. Reichenbach J, Reichstein M, Römermann C, Wittig A (2020) A virtual "Werkstatt" for digitization in the sciences. Research Ideas and Outcomes 6: e54106. https://doi.org/10.3897/rio.6.e54106
Figure 1 Integration of the "Werkstatt" in the Friedrich Schiller University and the research center of Jena.
Supplementary material 1 from: Galasso G, Domina G, Adorni M, Angiolini C, Apruzzese M, Ardenghi NMG, Assini S, Aversa M, Bacchetta G, Banfi E, Barberis G, Bartolucci F, Bernardo L, Bertolli A, Bonali F, Bonari G, Bonini I, Bracco F, Brundu G, Buccomino G, Buono S, Calvia G, Cambria S, Castagnini P, Ceschin S, Dagnino D, Di Gristina E, Di Turi A, Fascetti S, Ferretti G, Fois M, Gentili R, Gheza G, Gubellini L, Hofmann N, Iamonico D, Ilari A, Király A, Király G, Laface VLA, Lallai A, Lazzaro L, Lonati M, Longo D, Lozano V, Lupoletti J, Magrini S, Mainetti A, Manca M, Marchetti D, Mariani F, Mariotti MG, Masin RR, Mei G, Menini F, Merli M, Milani A, Minuto L, Mugnai M, Musarella CM, Olivieri N, Onnis L, Passalacqua NG, Peccenini S, Peruzzi L, Pica A, Pinzani L, Pittarello M, Podda L, Prosser F, Ravetto Enri S, Roma-Marzio F, Rosati L, Sarigu M, Scafidi F, Sciandrello S, Selvaggi A, Spampinato G, Stinca A, Tavilla G, Toffolo C, Tomasi G, Turcato C, Villano C, Nepi C (2020) Notulae to the Italian alien vascular flora: 9. Italian Botanist 9: 47-70. https://doi.org/10.3897/italianbotanist.9.53401
Supplementary data
Supplementary material 1 from: Bartolucci F, Domina G, Andreatta S, Angius R, Ardenghi NMG, Bacchetta G, Ballelli S, Banfi E, Barberis D, Barberis G, Bernardo L, Bertolli A, Bonari G, Bovio M, Briozzo I, Buccomino G, Calvia G, Chianese G, Cibei C, Conti F, Copez M, Crisanti A, Dagnino D, Di Filippo A, Esposito A, Fanni S, Festi F, Forte L, Galasso G, Gentili R, Gottschlich G, Lattanzi E, Liguori P, Locci MC, Longo D, Lonati M, Lucchese F, Marchetti D, Mariotti MG, Menini F, Minuto L, Orrù G, Pala ML, Passalacqua NG, Pellegrino M, Pennesi R, Peruzzi L, Pinzani L, Pirastru G, Prosser F, Ravetto Enri S, Roma-Marzio F, Russo G, Scoppola A, Silletti G, Stinca A, Toffolo C, Tomaselli V, Tondi G, Trenchi M, Turcato C, Nepi C (2020) Notulae to the Italian native vascular flora: 9. Italian Botanist 9: 71-86. https://doi.org/10.3897/italianbotanist.9.53429
Supplementary data
Supplementary material 1 from: Cunha MR, Génio L, Pradillon F, Clavel Henry M, Beaulieu S, Birch J, Campuzano FJ, Carretón M, De Leo F, Gula J, Laming S, Lindsay D, Matos FL, Metaxas A, Meyer-Kaiser K, Mills S, Queiroga H, Rodrigues CF, Sarrazin J, Watanabe H, Young R, Young CM (2020) Foresight Workshop on Advances in Ocean Biological Observations: a sustained system for deep-ocean meroplankton. Research Ideas and Outcomes 6: e54284. https://doi.org/10.3897/rio.6.e54284
Abstracts of keynote talks
Figure 2 from: Cunha MR, Génio L, Pradillon F, Clavel Henry M, Beaulieu S, Birch J, Campuzano FJ, Carretón M, De Leo F, Gula J, Laming S, Lindsay D, Matos FL, Metaxas A, Meyer-Kaiser K, Mills S, Queiroga H, Rodrigues CF, Sarrazin J, Watanabe H, Young R, Young CM (2020) Foresight Workshop on Advances in Ocean Biological Observations: a sustained system for deep-ocean meroplankton. Research Ideas and Outcomes 6: e54284. https://doi.org/10.3897/rio.6.e54284
Figure 2 Sustained meroplankton observations - a basin-scale approach. Low-cost samplers for deep-ocean observations (colonization modules coupled with larval traps) deployed at moorings or mounted on landers of the EMSO-ERIC distributed observatories and covering different water masses (Project LO3CATED; Génio, Cunha and Young). NACW: North Atlantic Central Water; AIW: Antarctic Intermediate Water; MOW: Mediterranean Outflow Water; NADW: North Atlantic Deep Water; MABW: Modified Antarctic Bottom Water.
Figure 1 from: Cunha MR, Génio L, Pradillon F, Clavel Henry M, Beaulieu S, Birch J, Campuzano FJ, Carretón M, De Leo F, Gula J, Laming S, Lindsay D, Matos FL, Metaxas A, Meyer-Kaiser K, Mills S, Queiroga H, Rodrigues CF, Sarrazin J, Watanabe H, Young R, Young CM (2020) Foresight Workshop on Advances in Ocean Biological Observations: a sustained system for deep-ocean meroplankton. Research Ideas and Outcomes 6: e54284. https://doi.org/10.3897/rio.6.e54284
Figure 1 Workshop participants "under the microscope" at the campus of Universidade de Aveiro: Back row, left to right: Fábio Matos, Jonathan Gula, Henrique Queiroga, Rob Young, Sven Laming, Kirstin Meyer-Kaiser, Jozée Sarrazin, Craig M. Young, Fabio De Leo. Front row, left to right: Jim Birch, Morane Clavel Henry, Marina R. Cunha, Clara Rodrigues, Florence Pradillon, Anna Metaxas.
Figure 7 from: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924
Figure 7 Hippocampus nalu in situ, juvenile, approximately 10 mm SL, Sodwana Bay, South Africa at 14 m depth (photograph Richard Smith / oceanrealmimages.com).
Figure 6 from: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924
Figure 6 Hippocampus nalu in situ, SAMC-F041934, paratype, male, Sodwana Bay, South Africa at 14 m depth (photograph Richard Smith / oceanrealmimages.com).
Figure 5 from: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924
Figure 5 Hippocampus nalu in situ, SAMC-F041933, holotype, female, Sodwana Bay, South Africa at 14 m depth (photograph Richard Smith / oceanrealmimages.com).
Figure 4 from: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924
Figure 4 Computed tomography scan of Hippocampus nalu, SAMC-F041933, holotype, female, 18.9 mm SL, 2 Mile Reef, Sodwana Bay, South Africa A lateral view of head and trunk area B anterolateral view of first and second superior trunk ridge spines (STrR1-2) C close-up lateral view of second superior trunk ridge cuspidate spines (STrR2). Abbreviations: ES, double eye spines; SOC, supraoccipital; CO, coronet; SC, supracleithrum; STrR1, first superior trunk ridge spine; STrR2, second superior trunk ridge spines; STrR5, fifth superior trunk ridge spine; STrR12, twelfth superior trunk ridge spine.
Figure 1 from: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924
Figure 1 Hippocampus nalu, preserved specimens A SAMC-F041933, holotype female, 18.9 mm SL, and B SAMC-F041934, paratype, male, 22 mm SL; South Africa: Sodwana Bay, 2 Mile Reef (photograph Australian Museum Research Institute).
Figure 2 from: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924
Figure 2 Computed tomography scanned skeleton of Hippocampus nalu, SAMC-F041933, holotype, 18.9 mm SL, female SLA ventral view B lateral view C dorsal view.
Figure 3 from: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924
Figure 3 Computed tomography scanned skeleton of Hippocampus nalu, SAMC-F041934, paratype, male, 22 mm SLA ventral view B lateral view C dorsal view.
Supplementary material 1 from: Ballelli S, Pennesi R, Campetella G, Cervellini M, Chelli S, Cianfaglione K, Lucarini D, Piermarteri K, Tardella FM, Catorci A, Canullo R (2020) An updated checklist of the vascular flora of Montagna di Torricchio State Nature Reserve (Marche, Italy). Italian Botanist 9: 87-100. https://doi.org/10.3897/italianbotanist.9.50032
Supplementary materials
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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.