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Fig. 6 in The palm (Arecaceae) collections gathered by Bonpland and Humboldt in their American journey: origin and fate of the specimens and typifications
Fig. 6. – List of palm common names written by Bonpland in the first page of the "Journal Botanique" (MS 1332). 1) "Cucurito" (Attalea maripa (Aubl.) Mart.); 2) "Seje" (Oenocarpus sp.); 3) "Volador" (Desmoncus sp.); 4) "Pijiguao" (Bactris gasipaes Kunth); 5) "Macana" (Euterpe sp.); 6) "Palmiche" (Copernicia tectorum Kunth); 7) "Palma de Cobija" (Copernicia tectorum Kunth); 8) "Timiti" (Manicaria saccifera Gaertn.); 9) "Cocos" (Cocos nucifera L.); 10) "Corozo" (Acrocomia aculeata (Jacq.) Lodd. ex Mart.); 11) "Prasse" (unknown Palmae); 12) "Jagua" (Attalea butyracea (Mutis ex L. f.) Wess. Boer; 13) "Moriche" (Mauritia flexuosa L.f.); 14) Piritu (Bactris guineensis (L.) H.E. Moore); 15) "Palma Real de Caracas" (Roystonea oleracea (Jacq.) O.F.Cook; 16) "Id. de Guanare" (prob. Roystonea sp.); 17) "Palma de Sombrero" (Sabal mauritiiformis (H. Karst.) Griseb. & H. Wendl.); 18) "Amac." (unknown Palmae); 19) "Alvarico" (Bactris sp); 20) "Joropa" (Palmae); 21) Tirite (Ischnosiphon arouma (Aubl.) KÖrn. Marantaceae); 22) "Chiquichiqui" (Leopoldinia piassaba Wallace); 23) "Iounouriri" (Attalea sp.).
Fig. 2 in The palm (Arecaceae) collections gathered by Bonpland and Humboldt in their American journey: origin and fate of the specimens and typifications
Fig. 2. – Representative palm specimens collected by Bonpland and Humboldt deposited in P. A. Ceroxylon andicolum Bonpl.; B. Corypha maritima Kunth; C. Corypha tectorum Kunth; D. Martinezia caryotifolia Kunth.
Fig. 5 in The palm (Arecaceae) collections gathered by Bonpland and Humboldt in their American journey: origin and fate of the specimens and typifications
Fig. 5. – Page of the "Journal Botanique" (MS 1332) of Bonpland and Humboldt compiled during their journey in Venezuela. The entry 1276 was written by Humboldt and corresponds to the collection of the royal Cuban palm Oreodoxa regia Humboldt & Bonpland ex Kunth (= Roystonea regia (Humboldt & Bonpland ex Kunth) O.F. Cook).
Data of two neotropical Colaptes woodpeckers' nests fate and environmental features associated with them
<p><span>Understanding factors affecting nest survival of woodpeckers in threatened landscapes is a key tool for land managers, particularly when conservation depends on public policies. However, information of Neotropical woodpeckers breeding in southern temperate forests is noticeably sparse despite the worrying conservation status of these ecosystems and woodpeckers' key role as cavity providers. Our objective was to assess the relationship between tree cavity features, vegetation structure, and landscape configuration on the nest survival of the Green-barred Woodpecker (<em>Colaptes</em> <em>melanochloros</em>) and the Campo Flicker (<em>C</em>. <em>campestris</em>). We monitored nests of these woodpeckers during three breeding seasons from 2015–2018 in a woodland of east-central Argentina threatened by selective tree logging and soil material extraction. We recorded features that presumably influence nest survival at a micro-scale (cavity, cavity-tree features, and foliage cover around the cavity) and a macro-scale (forest cover and shape index within a 500 m circle around the nest). We did not find support for a relationship between daily nest survival rates (DSR) and cavity features, vegetation structure, or landscape configuration. However, </span><span>new cavities were more successful than reused ones for the Green-barred Woodpecker. We also found a surprisingly high rate (~33% of nest failures) of nest abandonment for both species. Abandonment may be a factor regulating this population and causes of abandonment warrants further investigation. Given the importance of new cavities to the success of Green-barred Woodpeckers, our results indicate the preservation of medium-size trees (20 cm < DBH < 50 cm) with wood softened by degradation processes (preferred by the species to excavate cavities) would facilitate persistence of both of this woodpecker and the cavity-nesting community. Effective audit of soil material extraction and controlled selective timber logging practices (including preservation of mature trees) in compliance with existing regulations could contribute to this type of habitat maintenance.</span></p>
Fig. 3 in Climate change and the fate of endemic Beyşehir Frog, Pelophylax caralitanus
Fig. 3. Current climatic habitat suitability map (A) and the eight RCP climatic change scenario maps for P. caralitanus based on RCP 2.6 (B–C), RCP 4.5 (D–E), RCP 6.0 (F–G), and RCP 8.5 (H–I) for either 2050 or 2070 as indicated.
Fig. 2 in Climate change and the fate of endemic Beyşehir Frog, Pelophylax caralitanus
Fig. 2. Variables with the highest contributions to the potential distribution of P. caralitanus according to MAXENT with the standard errors in blue. The Y-axis indicates the probability of presence (based on the Cloglog, or complementary log-log transform, values) and the X-axis shows the contribution of each variable.
Fig. 10 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 10. Comparisons of inflammatory cells recruited to inflammatory foci in cane toads, Rhinella marina (a) and native frogs, Cyclorana australis (b). Each anuran species was exposed to infective larvae of Rhabdias hylae (white bars) and Rhabdias pseudosphaerocephala (grey bars). Graphs show average values ± 1 S.E.M.
Fig. 7 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 7. Histological investigation of lungworm infection in anurans. Graphs show the proportion of (a) metamorph native frogs (Cyclorana australis) and (b) metamorph cane toads (Rhinella marina) infected with lungworms, not infected with lungworms, or with inflammatory 'foci' (probable cases of a lungworm larva penetrating the anuran's body but failing to survive).
Fig. 2 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 2. The distribution of lungworm larvae in cane toad metamorphs. (a) Toad metamorphs infected with Rhabdias hylae (native frog lungworm) and (b) toad metamorphs infected with Rhabdias pseudosphaerocephala (cane toad lungworm). Data in panel (b) are from Pizzatto et al. (2010), with permission. LUNG refers to adult lungworms found within the lung, SKIN/MUSCLE refers to larvae found in the skeletal muscle or subcutaneous tissue, HEAD refers to larvae detected in the head or neck region (excluding those found in eye tissue), EYE indicates larvae found in the eye or periocular tissue, and COELOM denotes larvae within the coelom or coelomic membranes.
Fig. 1. Histological image depicting a in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 1. Histological image depicting a transverse section of (a) R. hylae larva in the connective tissue of the head of a cane toad and (b) the inflammatory response composed primarily of macrophages and multinucleated giant cells surrounding the parasite. Haematoxylin and eosin stain, 400× magnification, scale bar equals 30 μm.
Fig. 4 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 4. Effect of time since exposure to Rhabdias hylae larvae on cane toad metamorphs: (a) shows the number of larvae found in toads and (b) shows the number of foci (areas of inflammation with no visible larvae) in toads, as determined by histological methods.
Fig. 9 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 9. Change in the average number of inflammatory foci (probable cases of larval parasites breaking down) observed in all anurans over time. Graph shows average values ± 1 S.E.M.
Fig. 6 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 6. Effects of Rhabdias hylae infection on cane toad metamorphs: (a) the average percentage of neutrophils and (b) lymphocytes around inflammation sites over time in cane toads infected with Rhabdias hylae. Graphs show average values ±1 S.E.M.
Fig. 3 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 3. The state of Rhabdias hylae larvae in cane toads as a function of days-post treatment. The graph shows larval numbers as the percentage of total larvae that were seen at each time period.
Fig. 5 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 5. Average inflammation severity surrounding Rhabdias hylae larvae and foci (probable larvae being broken down by the host's immune system) within infected cane toads at different numbers of days post-infection. Graph shows average values ±1 S.E.M.
Fig. 8 in Host-parasite interactions during a biological invasion: The fate of lungworms (Rhabdias spp.) inside native and novel anuran hosts
Fig. 8. Changes through time (days post-infection) on the relative numbers of anurans that were infected with lungworms, and that contained adult versus juvenile stages of the parasites involved. Data are shown for two lungworm species (Rhabdias hylae from native frogs, and Rhabdias pseudosphaerocephala from invasive cane toads) and for two types of host: the native frog, Cyclorana australis, and the cane toad, Rhinella marina. The panels show data for (a) C. australis infected with R. pseudosphaerocephala, (b) C. australis infected with R. hylae, (c) cane toads infected with R. pseudosphaerocephala and (d) cane toads infected with R. hylae.
Fig. 2 Micromorphological differences between Drepanocladus longifolius and D in Do Antarctic populations represent local or widespread phylogenetic and ecological lineages? Complicated fate of bipolar moss concepts with Drepanocladus longifolius as a case study
Fig. 2 Micromorphological differences between Drepanocladus longifolius and D. capillifolius. Alar cells of D. longifolius a, b—from Lyall 47, Falkland Islands. Alar cells of D. capillifolius c―from Nelson 4262, USA, Wyoming (KRAM), d―from isolectotype of Hypnum capillifolium var. fallax Renauld, Canada, Quebec. Scale bar 100 μm
Fig. 1 in Do Antarctic populations represent local or widespread phylogenetic and ecological lineages? Complicated fate of bipolar moss concepts with Drepanocladus longifolius as a case study
Fig. 1 Geographical distribution of the studied accessions and detected genetic lineages corresponding to Drepanocladus longifolius (blue dots) and D. capillifolius (green triangles) according to present circumscription.
Data: In vivo fate of free and encapsulated iron oxide nanoparticles after injection of labelled stem cells
<p>This data set is composed of magnetic resonance images (MRI) that are supporting the article entitled <em>In vivo fate of free and encapsulated iron oxide nanoparticles after injection of labelled stem cells </em>by the same authors. Nanoparticle contrast agents are used to label stem cells and monitor their bio-distribution in pre-clinical models of disease. Due to the impact on the interpretation of imaging results, understanding the <em>in vivo</em> fate of the particles is important. The bio-distribution after intra-cardiac injection of labelled cells with superparamagnetic iron oxide nanoparticles was monitored longitudinally by MRI. </p>
Research data supporting "Fate of Liposomes in Presence of Phospholipase C and D: From Atomic to Supramolecular Lipid Arrangement"
<p>Raw research data for experimental work supporting the publication above.</p> <p>Raw data for MD simulation is available upon reasonable request from Irene Yarovsky (irene.yarovsky@rmit.edu.au).</p>
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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.