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5,145 results for “CO₂”
Data analysis on the healthcare personnel engaged in type 2 diabetes treatments and their communication activities as part of Co-exploration Activity 1
<p>This analysis compared the findings from two health-service guidelines and the feedback from the health professionals who participated in Co-design Activity 1 to delineate patient journeys through type 2 diabetes treatments. The patent journeys described the healthcare personnel (health professionals and auxiliary staff) engaged in the treatments, communication activities, and the relevant health contents they commonly deliver to diabetic patients.</p>
Data analyses of Co-exploration Activity 2
<p>These datasets are the appendices of the analyses for Co-exploration Activity 2 of Chininthorn's Ph.D. thesis. </p> <p> </p>
Figure 2 from: Andrino CO, Barbosa-Silva RG, Lovo J, Viana PL, Moro MF, Zappi DC (2020) Iron islands in the Amazon: investigating plant beta diversity of canga outcrops. PhytoKeys 165: 1-25. https://doi.org/10.3897/phytokeys.165.54819
Figure 2 Representative species of canga in new dataset, SFXaAxonopus longispicus (Döll) Kuhlm bDicypellium aff. caryophyllaceum (Mart.) Nees cInga heterophylla Willd dIpomoea decora Meisn eMatelea microphylla Morillo fMimosa dasilvae A.S.L. Silva & Secco gNepsera aquatica (Aubl.) Naudin hOuratea cearensis (Tiegh.) Sastre & Offroy iPachyptera incarnata (Aubl.) Francisco & L.G. Lohmann jPassifora picturata Ker Gawl. kPhyllanthus minutulus Mull.Arg. lRodriguezia lanceolata Ruiz & Pav.
Figure 1 from: Andrino CO, Barbosa-Silva RG, Lovo J, Viana PL, Moro MF, Zappi DC (2020) Iron islands in the Amazon: investigating plant beta diversity of canga outcrops. PhytoKeys 165: 1-25. https://doi.org/10.3897/phytokeys.165.54819
Figure 1 a Geographic location of the present study site at SFX and the other study areas from Carajás complex b aerial view of an island of canga vegetation surrounding by the rainforest (Photo: Leonardo Vianna) cSerra de Campos of São Félix do Xingu (SFX) phytophysiognomy with shrubby and grassy vegetation.
Supplementary material 1 from: Andrino CO, Barbosa-Silva RG, Lovo J, Viana PL, Moro MF, Zappi DC (2020) Iron islands in the Amazon: investigating plant beta diversity of canga outcrops. PhytoKeys 165: 1-25. https://doi.org/10.3897/phytokeys.165.54819
Investigating plant beta diversity of canga outcrops
Figure 4 from: Andrino CO, Barbosa-Silva RG, Lovo J, Viana PL, Moro MF, Zappi DC (2020) Iron islands in the Amazon: investigating plant beta diversity of canga outcrops. PhytoKeys 165: 1-25. https://doi.org/10.3897/phytokeys.165.54819
Figure 4 a Species richness plotted against area of Carajás. Pearson correlation coefficients: r = 0.806094, P = 0.001548 b the number of species shared between site pairs does not change significantly with geographical distance between regions. r = -0.16; P = 0.08 c the number of shared endemic species between site pairs declines with geographical distance between regions. r= -0.45872; P = 1.37e-07.
Figure 3 from: Andrino CO, Barbosa-Silva RG, Lovo J, Viana PL, Moro MF, Zappi DC (2020) Iron islands in the Amazon: investigating plant beta diversity of canga outcrops. PhytoKeys 165: 1-25. https://doi.org/10.3897/phytokeys.165.54819
Figure 3 UPGMA (a) and NMDS (b) multivariate analysis clustering areas from FCC and SFX (see Table 2 for area codes). UPGMA cophenetic coefficient: 0.902. b. NMDS stress: 0.1859.
Figure 2 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 2 Original figures ABuccinum nucleus Bruguière, 1789 (Lister 1770: pl. 976, fig. 32) BPlanaxis semisulcatus G.B. Sowerby I, 1823 ([pl. 73], fig. 3).
Figure 3 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 3 Type specimens of Supplanaxis nucleus and relevant planaxids. ABuccinum nucleus Bruguière, 1789. Neotype, MNHN-IM-2000-35804 BPlanaxis planicostatus G.B. Sowerby I, 1825. Syntype NHMUK 1966623 (© The Trustees of the Natural History Museum, London, http://creativecommons.org/licenses/by/4.0/; https://data.nhm.ac.uk/object/4767541c-a5d1-41db-aa0c-0c03724e970a) CPlanaxis (Supplanaxis) nancyae Petuch, 2013. Holotype, FMNH 328402 (© Field Museum of Natural History–CC BY-NC; https://collections-zoology.fieldmuseum.org/catalogue/2877223) DPlanaxis niger Quoy and Gaimard, 1833. Syntype, one of 22 specimens, MNHN-IM-2000-27769 EPlanaxis nucleola Mörch, 1876. Probable holotype, ZMK 152749. Scale bar: 1 cm.
Figure 6 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 6 Radular morphology of Supplanaxis nancyae (MNHN-IM-2019-1703, except as noted) A Radular ribbon B Rachidian and lateral teeth C Detail of lateral teeth D Detail of rachidian. Note fusion of innermost denticle with central cusp E Rachidian and lateral teeth viewed at a ~ 45° angle from above, showing detail of cutting edge F Internal and external lateral teeth (MNHN-IM-2019-1704). Scale bars: 200 µm (A), 50 µm (B, C, D, E, F).
Figure 1 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 1 Phylogenetic tree produced via Maximum Likelihood using a concatenated alignment composed of partial mitochondrial COI and 16S sequences. ML bootstrap values greater than 50 are shown at the nodes. Figured specimens: Supplanaxis nancyae, MNHN-IM-2019-1729; S. planicostatus, syntype, NHMUK 1966623; S. nucleus, neotype, MNHN-IM-2000-35804.
Figure 8 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 8 Habitat A Curaçao, S shore, beach in front of CARMABI research station BSupplanaxis nucleus and S. nancyae individuals among cobbles.
Figure 5 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 5 Radular morphology of Supplanaxis nucleus (MNHN-IM-2019-1716) A Radular ribbon B Rachidian and lateral teeth C Detail of lateral teeth D Detail of rachidian E Rachidian and lateral teeth viewed at a ~ 45° angle from above, showing detail of cutting edge. F Internal and external lateral teeth. Scale bars: 200 µm (A), 100 µm (B, E), 50 µm (C, D, F).
Figure 4 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 4 Shell morphology of Supplanaxis from the Caribbean. Sequenced vouchers A–GS. nucleusH–OS. nancyaeA–C Guadeloupe, Plage de Malendure AMNHN-IM-2019-1716 BMNHN-IM-2009-26686 CMNHN-IM-2009-26687 D–E Barbados, Hastings Rocks. D Neotype, MNHN-IM-2000-35804 EMNHN-IM-2019-1728 F–G Curaçao, S shore, beach in front of CARMABI research station FUSNM 1618956 GUSNM 1618953 H–J Guadeloupe, Plage de Malendure HMNHN-IM-2019-1703 IMNHN-IM-2019-1704 J IM MNHN-2009-26684 K–L Barbados, Hastings Rocks KMNHN-IM-2019-1729 LMNHN-IM-2019-1711 M–O Curaçao, S shore, beach in front of CARMABI research station MUSNM 1618949 NUSNM 1618951 OUSNM 1618952. Scale bar: 1 cm.
Figure 7 from: Strong EE, Bouchet P (2020) Hidden in plain sight: two co-occurring cryptic species of Supplanaxis in the Caribbean (Cerithioidea, Planaxidae). ZooKeys 991: 85-109. https://doi.org/10.3897/zookeys.991.57521
Figure 7 Comparative shell morphology of Supplanaxis around the Caribbean. Supplanaxis nancyae is shown at left, and S. nucleus is at right, for each pair. The individuals from each pair were sampled from the same site and were originally part of the same lot A Florida, Miami Beach, South Beach, at jetty (at left, USNM 1620287; at right, USNM 842270) B Bahamas, New Providence, The Caves (at left, USNM 1620274; at right, USNM 603895) C Mexico, Cozumel, 1 mi. N of San Miguel (at left, USNM 1620276; at right, USNM 662773) D Jamaica, St. Mary, 2 mi. N Port Maria (at left, USNM 1620285; at right, USNM 770590) E Dominican Republic, Oro Oro Beach [sic, possibly Playa Dorada], S. shore (at left, USNM 1620275; at right, USNM 603900) F Virgin Islands, St. John, Caneel Bay (at left, USNM 1620284; at right, USNM 738775) G Antigua and Barbuda, Antigua, Green Id. (at left, USNM 1620283; at right, USNM 738725) H Honduras, Utilla Id. (at left, USNM 1620264; at right, USNM 434879) I Panama, Puerto Perme, NW of Cape Tiburon (at left, USNM 1620279; at right, USNM 664216) J Curaçao, S shore, beach in front of CARMABI research station (at left, USNM 1618952; at right USNM 1618956; sequenced vouchers) K Guadeloupe, Plage de Malendure (at left, MNHN-IM-2019-1703; at right MNHN-IM-2009-26687; sequenced vouchers) L Barbados, Hastings Rocks (at left, MNHN-IM-2019-1729; at right, neotype, MNHN-IM-2000-35804; sequenced vouchers). Base map: Wikimedia Commons contributors (2017).
Looks can be deceiving: speciation dynamics of co-distributed Angophora (Myrtaceae) species in a varying landscape
<p>Understanding the mechanisms underlying species divergence remains a central goal in evolutionary biology. Landscape genetics can be a powerful tool for examining evolutionary processes. We used genome-wide scans to genotype samples from populations of eight <i>Angophora</i> species. <i>Angophora</i> is a small genus within the eucalypts comprising common and rare species in a heterogeneous landscape, making it an appropriate group to study speciation. We found <i>A. hispida</i> was highly differentiated from the other species. Two subspecies of <i>A. costata</i> (subsp. <i>costata</i> and subsp. <i>euryphylla</i>) formed a group, while the third (subsp. <i>leiocarpa, </i>which is only distinguished by its smooth fruits and provenance) was supported as a distinct pseudocryptic species. Other species that are morphologically distinct could not be genetically differentiated (e.g., <em>A. floribunda </em>and <em>A. subvelutina</em>). Distribution and genetic differentiation within <i>Angophora</i> were strongly influenced by temperature and humidity, as well as biogeographic barriers, particularly rivers and higher elevation regions. While extensive introgression was found between many populations of some species (e.g., <i>A. bakeri</i> and <i>A. floribunda</i>), others only hybridized at certain locations. Overall, our findings suggest multiple mechanisms drove evolutionary diversification in <em>Angophora</em> and highlight how genome-wide analyses of related species in a diverse landscape can provide insights into speciation. </p>
Figure 6 from: Gonella PM, Barbosa-Silva RG, Fleischmann AS, Zappi DC, Baleeiro PC, Andrino CO (2020) Hidden biodiversity of Amazonian white-sand ecosystems: two distinctive new species of Utricularia (Lentibulariaceae) from Pará, Brazil. PhytoKeys 169: 75-98. https://doi.org/10.3897/phytokeys.169.57626
Figure 6 SEM microphotographs of seeds of Utricularia jaramacaru at 420× magnification, in dorsal, lateral and oblique view (from the holotype).
Figure 5 from: Gonella PM, Barbosa-Silva RG, Fleischmann AS, Zappi DC, Baleeiro PC, Andrino CO (2020) Hidden biodiversity of Amazonian white-sand ecosystems: two distinctive new species of Utricularia (Lentibulariaceae) from Pará, Brazil. PhytoKeys 169: 75-98. https://doi.org/10.3897/phytokeys.169.57626
Figure 5 Utricularia jaramacarua inflorescence apex with open flowers and bud b detail of inflorescence apex showing mucilage droplet in the axil of a pedicel c inflorescence apex with a flower in posterior view, highlighting the calyx (c1) d flower in anterior view; e, peduncle bases with stolons and leaves.
Figure 3 from: Gonella PM, Barbosa-Silva RG, Fleischmann AS, Zappi DC, Baleeiro PC, Andrino CO (2020) Hidden biodiversity of Amazonian white-sand ecosystems: two distinctive new species of Utricularia (Lentibulariaceae) from Pará, Brazil. PhytoKeys 169: 75-98. https://doi.org/10.3897/phytokeys.169.57626
Figure 3 Utricularia arirambaa inflorescence apex with flowers and bud of the white corolla morphotype, showing the reflexed apex of lower corolla lip b flowers of the lavender corolla morphotype, with a calyx of a developing fruit to the left c flower of the white corolla morphotype in posterior view, showing the calyx lobes and the concavity in the ventral portion of the spur d flowers of the lavender corolla morphotype e inflorescence apex of the white corolla morphotype showing variation in spur morphology.
Figure 1 from: Gonella PM, Barbosa-Silva RG, Fleischmann AS, Zappi DC, Baleeiro PC, Andrino CO (2020) Hidden biodiversity of Amazonian white-sand ecosystems: two distinctive new species of Utricularia (Lentibulariaceae) from Pará, Brazil. PhytoKeys 169: 75-98. https://doi.org/10.3897/phytokeys.169.57626
Figure 1 Distribution map of the new species of Utricularia in the Amazon. On the left map, the main rivers of the hydrographic basin of the region and which cross the FLOTA Trombetas (highlighted in green). The map to the right shows the records of Utricularia ariramba (squares) and Utricularia jaramacaru (triangle), which are near the FLOTA limits, as well the as threats to the area, including recent fires, full deforestation, and selective deforestation of timber species.
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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.