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Figures 22-26 from: da Silva HAM, Silva-Soares T, de Brito-Gitirana L (2017) Comparative analysis of the integument of different tree frog species from Ololygon and Scinax genera (Anura: Hylidae). Zoologia 34: 1-17. https://doi.org/10.3897/zoologia.34.e20176
Figures 22-26 - Light micrograph of the integument of S. hayii: (22) Dorsal region (Mallory´s trichrome staining); (23) Dorsal region (AB-method); (24) Ventrolateral region (HE-staining) (25) Ventral region (AB-method); (26) Ventral region (HE-staining). In the dorsal integument, exocrine glands are more frequent, mainly the serous glands (Ø). Melanophores (_) occur in the spongious dermis, even around the secretory portion of glands. Note clusters of apocrine glands with heterogeneous content (¬)in the spongious dermis of the ventrolateral integument. The EK-layer (Æ) is continuous in the dorsal integument, but absent in the ventral region. Slight cutaneous elevations (á) in the ventral integument are formed by the epidermis and the dermis, mainly the spongious dermis. They are separated by groves (). CD = compact dermis.
Figures 18-21 from: da Silva HAM, Silva-Soares T, de Brito-Gitirana L (2017) Comparative analysis of the integument of different tree frog species from Ololygon and Scinax genera (Anura: Hylidae). Zoologia 34: 1-17. https://doi.org/10.3897/zoologia.34.e20176
Figures 18-21 - Light micrograph of the integument of O. flavoguttata: (18) Dorsal region (HE-staining); (19) Dorsal region (AB-method); (20) Ventrolateral region (HE-staining) (21) Ventral region (HE-staining). The epidermis (E) is partially keratinized, and the outermost cell layer exhibits the nuclear profiles (→). Melanophores (_) occur in the spongious dermis of both dorsal and ventrolateral regions; they are more frequent in the dorsal integument. Small clusters of apocrine glands with heterogeneous content occur in the ventrolateral integument. In the ventral region, the lipid content (ë), mixed with basophilic material, is easily visualized in the apocrine glands (Fig. 21). In the dorsal region, the EK-layer () is continuous, but discontinuous in the ventrolateral integument, being less alcianophilic in the ventral region when compared to other integument regions. CD = compact dermis; H = hypodermis.
Figures 32-35 from: da Silva HAM, Silva-Soares T, de Brito-Gitirana L (2017) Comparative analysis of the integument of different tree frog species from Ololygon and Scinax genera (Anura: Hylidae). Zoologia 34: 1-17. https://doi.org/10.3897/zoologia.34.e20176
Figures 32-35 - Light micrograph of the integument of O. perpusilla: (32) Dorsal region (HE-staining); (33) Dorsal region (AB-method); (34) Ventrolateral region (HE-staining) (35) Ventral region (AB-method). The spongious dermis houses both apocrine glands with heterogeneous content (¬) and serous glands (Ø). Melanophores (_) occur in the dorsal integument, but they are not identified in either the ventrolateral or ventral region. Iridophores did not occur in all integument regions. The EK-layer (Æ) is a well defined continuous layer occurs as irregular deposits between the spongious and compact dermis of the ventral region. Cutaneous elevations (â) are separated by grooves (Ú) in the ventral region. CD = compact dermis.
Figures 14-17 from: da Silva HAM, Silva-Soares T, de Brito-Gitirana L (2017) Comparative analysis of the integument of different tree frog species from Ololygon and Scinax genera (Anura: Hylidae). Zoologia 34: 1-17. https://doi.org/10.3897/zoologia.34.e20176
Figures 14-17 - Light micrograph of the integument of O. angrensis: (14) Dorsal region (AB-staining); (15) Ventrolateral region (HE-staining), inset (Mallory´s trichrome staining); (16) Ventral region (HE-staining); (17) Ventral region (AB-method). The melanophores (_) are numerous and located just beneath of the epidermis as well as around de glandular secretory units. They occur also in the hypodermis, but absent in the ventral integument. Iridophores (→) occur in the spongious dermis of the dorsal region just beneath the epidermis. No iridophore is visualized in the ventral region of the integument. Clusters of apocrine glands (¬) with heterogeneous intake predominate at ventrolateral integument; inset of Fig. 15: Observe the granular content with dense stained core () intermingled with cytoplasm material (*). The EK-layer () is continuous in the ventral region, but discontinuous in the ventral integument. Serous glands (Ø) occur in all body regions. Note blood vessels (Æ) in the spongious dermis. CD = compact dermis.
Figures 52-55 from: da Silva HAM, Silva-Soares T, de Brito-Gitirana L (2017) Comparative analysis of the integument of different tree frog species from Ololygon and Scinax genera (Anura: Hylidae). Zoologia 34: 1-17. https://doi.org/10.3897/zoologia.34.e20176
Figures 52-55 - Light micrograph of the integument of S. x-signatus: (52) Dorsal region (HE-staining); (53) Dorsal region (AB-method); (54) Ventrolateral region (Mallory´s trichrome staining); (55) Ventral region (Mallory´s trichrome staining). The epidermis (E) is slightly ticker when compared to those of other hylids, as in the compact dermis (CD). Melanophores (_) are visulized in both dorsal and ventrolateral integument just beneath the epidermis. Serous glands are present in all regions; however, some of them show slightly alcianophilic content (→) in both ventrolateral and ventral regions. The apocrine glands (¬) with granular content occur in both dorsal and ventrolateral regions. The EK-layer (Æ) is visualized in both dorsal and ventrolateral integument but is absent in the ventral integument.
Figure 5 from: Caraballo-Ortiz MA, Trejo-Torres JC (2017) Two new endemic tree species from Puerto Rico: Pisonia horneae and Pisonia roqueae (Nyctaginaceae). PhytoKeys 86: 97-115. https://doi.org/10.3897/phytokeys.86.11249
Figure 5 - Pisonia roqueae. A Foliage B Adaxial side of mature leaves C Twig with ferrugineous-brownish pubescence, turning grayish as it ages D Pistillate inflorescence and young leaves E Ripe infructescence F Trunk of an adult tree. Photo credits: A–C, F: Fabiola Areces (Areces Berazain et al. 2013-2017); D–E: JCTT.
Figure 4 from: Caraballo-Ortiz MA, Trejo-Torres JC (2017) Two new endemic tree species from Puerto Rico: Pisonia horneae and Pisonia roqueae (Nyctaginaceae). PhytoKeys 86: 97-115. https://doi.org/10.3897/phytokeys.86.11249
Figure 4 - Fruits of the six species of Pisonia from Puerto Rico. A P. aculeata B P. albida C P. horneae D P. roqueae E P. subcordata F P. taina. Reference specimens: A Rose 3548, US B Little 13219, US C Acevedo-Rdgz. 13404, US D Proctor 44432, US E Breckon 7766, US; and F Trejo 2371, US.
Figure 3 from: Caraballo-Ortiz MA, Trejo-Torres JC (2017) Two new endemic tree species from Puerto Rico: Pisonia horneae and Pisonia roqueae (Nyctaginaceae). PhytoKeys 86: 97-115. https://doi.org/10.3897/phytokeys.86.11249
Figure 3 - Distribution of Pisonia (excluding P. aculeata) in Puerto Rico and adjacent islands based on herbarium specimens. Empty symbols represent historical localities where populations have been presumably extirpated (see Trejo-Torres 2005 and this study for details).
Figure 6 from: Caraballo-Ortiz MA, Trejo-Torres JC (2017) Two new endemic tree species from Puerto Rico: Pisonia horneae and Pisonia roqueae (Nyctaginaceae). PhytoKeys 86: 97-115. https://doi.org/10.3897/phytokeys.86.11249
Figure 6 - Holotype specimen of Pisonia roqueae from the National Herbarium of the Smithsonian Institution (Proctor et al. 48064, US [00707324]). Note the dendroid staminate inflorescences with globose crowns and the leafless branches during the flowering period. Photo courtesy of The United States National Herbarium, Smithsonian Institution.
Figure 2 from: Caraballo-Ortiz MA, Trejo-Torres JC (2017) Two new endemic tree species from Puerto Rico: Pisonia horneae and Pisonia roqueae (Nyctaginaceae). PhytoKeys 86: 97-115. https://doi.org/10.3897/phytokeys.86.11249
Figure 2 - Isotype specimen of Pisonia horneae from the University of Florida Herbarium (Trejo et al. 2310, FLAS [230768]). Photo courtesy of The University of Florida Herbarium (FLAS) – Florida Museum of Natural History.
Figure 1 from: Caraballo-Ortiz MA, Trejo-Torres JC (2017) Two new endemic tree species from Puerto Rico: Pisonia horneae and Pisonia roqueae (Nyctaginaceae). PhytoKeys 86: 97-115. https://doi.org/10.3897/phytokeys.86.11249
Figure 1 - Pisonia horneae. A Branch showing adaxial side of leaves B Abaxial side of leaves C Staminate (left) and pistilate (right) flowers at anthesis D Seedlings E Bark F Lower trunk of an adult tree. Note the characteristic swollen base observed in all Pisonia from Puerto Rico, where the trunk base wraps over the rocks as it grows. Photo credits: A–B, E–F: JCTT; C–D: MACO.
Fig. 6. – Dalbergia rajeryi N in Taxonomic studies on Malagasy Dalbergia (Fabaceae). V. Eight new large tree species and notes on related Malagasy species
Fig. 6. – Dalbergia rajeryi N. Wilding, Phillipson & Crameri. A. Fruiting branch (immature infrutescence); B. Mature fruit; C. Leaflet upper surface; D. Leaflet lower surface; E. Inflorescence; F. Flower; G. Calyx (outer surface, split open and flattened); H. Standard petal (adaxial surface); I. Wing petal (adaxial surface); J. Keel petal (adaxial surface); K. Androecium (adaxial surface, flattened). L. Gynoecium.
Fig. 3. – Dalbergia karatrae N in Taxonomic studies on Malagasy Dalbergia (Fabaceae). V. Eight new large tree species and notes on related Malagasy species
Fig. 3. – Dalbergia karatrae N. Wilding, Phillipson & Crameri. A. Flowering branch; B. Portion of leaf rachis with leaflets (lower surface); C. Infructescence; D. Flower; E. Calyx (outer surface, split open and flattened); F.Standard petal (adaxial surface);
Baseline and Future Habitat Suitability Maps for Tree Species Prioritized for Food Tree Portfolios for Zambia
<p>This archive includes habitat suitability maps for six native food tree species (<em>Anisophyllea boehmii</em> Engl., <em>Parinari curatellifolia</em> Planch. ex Benth., <em>Strychnos cocculoides</em> Baker, <em>Tamarindus indica </em>L., <em>Thespesia garckeana </em>F.Hoffm. [syn. <em>Azanza garckeana </em>(F.Hoffm.) Exell & Hillc.] and <em>Uapaca kirkiana</em>|Müll.Arg.|) and four exotic food tree species (<em>Carica papaya</em> L., <em>Mangifera indica</em> L., <em>Persea americana</em> Mill. and <em>Psidium guajava</em> L.). These species had been prioritized by the project. Species suitability modelling followed the BIOCLIM algorithm whereby a climate suitability score is calculated that reflects the core distribution (5% - 95%) and the marginal distribution (0% - 5% or 95% or 100%) of a species in environmental space. The BIOCLIM algorithm was expanded to reflect the middle of the environmental range (25% - 75%).</p> <p>Species suitability was inferred through bioclimatic ranges documented in the Tree Globally Observed Environmental Ranges database (TreeGOER; Kindt <a href="https://onlinelibrary.wiley.com/doi/10.1111/gcb.16914">2023</a>). Baseline suitability maps used the historical climate documented by WorldClim 2.1 (Fick & Hijmans <a href="https://doi.org/10.1002/joc.5086">2017</a>). Future suitability maps correspond to a low emissions scenario (Shared Socio-Economic Pathway [SSP] 1-2.6) and a high emissions scenario (SSP 3-7.0), both calculated as medians from Global Climate Models (GCM) projections for the 2050s (2041-2060) available from WorldClim 2.1 (respectively from 23 and 18 GCMs).</p> <p>For larger sets of tree species native to Zambia, it has recently become possible to filter tree species by bioclimatic conditions of the planting site with the GlobalUsefulNativeTrees database (GlobUNT; Kindt et al. <a href="https://www.nature.com/articles/s41598-023-39552-1">2023</a>). The GlobUNT database internally uses TreeGOER environmental ranges and the same BIOCLIM algorithm that was used the generate the habitat suitability maps. Included in this archive is a list of native tree species to Zambia that were filtered for the use category of human food.</p> <p> </p> <p>When using these maps, cite the following:</p> <p>· Fick, S. E., & Hijmans, R. J. (2017). WorldClim 2: New 1‐km spatial resolution climate surfaces for global land areas. <em>International Journal of Climatology</em>, <em>37</em>(12), 4302–4315. <a href="https://doi.org/10.1002/joc.5086">https://doi.org/10.1002/joc.5086</a></p> <p>· Kindt, R. (2023). TreeGOER: A database with globally observed environmental ranges for 48,129 tree species. <em>Global Change Biology</em>, 29, 6303–6318. <a href="https://doi.org/10.1111/gcb.16914">https://doi.org/10.1111/gcb.16914</a></p> <p> </p> <p>Information in this archive were generated for the project of <strong>Piloting incentive-based agricultural portfolios for nutrition and resilience in Zambia</strong>. For more information about this project, check the website: <a href="https://www.worldagroforestry.org/project/piloting-incentive-based-agricultural-portfolios-nutrition-and-resilience-zambia">Piloting incentive-based agricultural portfolios for nutrition and resilience in Zambia | World Agroforestry | Transforming Lives and Landscapes with Trees</a></p>
Occurrence data for 18 tree species used in a common garden experiment
<p>Occurance data for 18 tropical rainforest tree species from across their home range downloaded from gbif, processed and used in the determination of ecoclimatic niche maps as part of work examinnig variation in growth and survival when grown under contrasting common garden sites</p>
Fig. 4 in Predicting the potential distribution of the subalpine broad-leaved tree species, Betula ermanii Cham. under climate change in South Korea
Fig. 4. The response curves for the two largest contributing variables for Betula ermanii under current climate conditions. Response curves indicate the correlation between the climatic variables and the probability of B. ermanii presence.
Fig. 5 in Predicting the potential distribution of the subalpine broad-leaved tree species, Betula ermanii Cham. under climate change in South Korea
Fig. 5. The potential distribution of Betula ermanii under current and future climatic conditions (2050s and 2070s) based on RCPs4.5 and 8.5 scenarios. A. Current. B. 2050s-RCP4.5. C. 2050s-RCP8.5. D. 2070s-RCP4.5. E. 2070s-RCP8.5. Blue dotted lines indicate the locations of potential habitat.
Fig. 3. A neighbor-joining phylogenetic tree reconstructed from a in Report of two unrecorded yeast species in the class Tremellomycetes
Fig. 3. A neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strain DJ2-14-10C with closely related species. Bootstrap values (>70%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position (Trees, 1987).
Figure 8 from: Yang J, Liu JK, Hyde KD, Jones EBG, Liu ZY (2018) New species in Dictyosporium, new combinations in Dictyocheirospora and an updated backbone tree for Dictyosporiaceae. MycoKeys 36: 83-105. https://doi.org/10.3897/mycokeys.36.27051
Figure 8 Dictyosporium nigroapice (MFLU18-1043). a Colonies on submerged wood b, c Conidia and conidiophores d–j Conidia k Germinated conidium l, m Culture, l from above, m from reverse. Scale bars: a = 100 μm, b, c, j = 20 μm, d–i = 10 μm, k = 30 μm.
Figure 6 from: Yang J, Liu JK, Hyde KD, Jones EBG, Liu ZY (2018) New species in Dictyosporium, new combinations in Dictyocheirospora and an updated backbone tree for Dictyosporiaceae. MycoKeys 36: 83-105. https://doi.org/10.3897/mycokeys.36.27051
Figure 6 Dictyosporium tratense (MFLU 18-1042, holotype). a Colonies on submerged wood b Squash mount of a sporodochium c Germinated conidium d–i Conidia j, k Culture j from above k from reverse. Scale bars: a = 200 μm, b = 50 μm, c = 30 μm, d–i = 20 μm.
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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.