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384 results for “epiphyte”
Fig. 30 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 30. Chaetonotus (Hystricochaetonotus) inaequabilis sp. nov. Adult specimen. Bright field microphotographs. A. Scales, dorsal view. B. Posterior trunk region, furca base and furcal appendage scales, dorsal view. C. Posterior trunk region, furca base and furcal appendage scales, ventral view.
Fig. 4 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 4. Chaetonotus (Chaetonotus) invitatus sp. nov. Schematic drawings of the spine types. A. Dorsal and dorsolateral spine type. B. Lateral and ventrolateral spine type. C. Ventral spine type. D. Scale 18 spine type. E. Dorsolateral furcal appendage spine type. F. Parafurcal spine type.
Fig. 1. Study area. A in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 1. Study area. A. The inside of Jubilee Greenhouse at the Botanical Garden in Kraków. B. Sampling site.
Supplementary material 1 from: Liu H-M, Shen J-Y, Liang Z-L, Peng F, Wang W-Z, Yang Z-W, Wang S, Parris B, Schneider H (2019) Two out of one: revising the diversity of the epiphytic fern genus Scleroglossum (Polypodiaceae, Grammitidoideae) in southern China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 115-133. https://doi.org/10.3897/phytokeys.130.33979
: Data type: Collection data
Figure 2 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 2 Total number of shared haplotypes between populations of Usnea subfloridana in the south-eastern (SE), the western (W) and northern (N) regions of Estonia; the thickness of lines reflects the number of shared haplotypes between populations.
Figure 3 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 3 Usnea subfloridana multilocus genotypes in the principal component analysis (PCA) ordination plot of the first and second axes. Samples are grouped according to the presence of lichen substance: samples containing thamnolic (square) or squamatic acid (circle).
Figure 1 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 1 Distribution map of Usnea subfloridana in Estonia (light grey squares) and study populations (black circles) on Hiiumaa island in the western region (W), in the south-eastern region (SE) and in the northern region of Estonia; the map of Scandinavia was taken from free map resource http://d-maps.com/carte.php?num_car=5977&lang=en.
Figure 6 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 6 Alleles of Usnea subfloridana and explanatory variables mean annual air temperature ('Temp') and geographical longitude of populations ('Long') in the bi-plot of the redundancy analysis (RDA) of the first and second axes. Labels of alleles prefixed by '8' or '9' indicate that these alleles belong to loci Us08 or Us09, respectively; for example, 8201 means that allele 201 is from Us08
Figure 4 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 4 Usnea subfloridana multilocus genotypes (Us02, Us03, Us04, Us05, Us06, Us08, Us09) and explanatory variables mean annual air temperature ('Temp') and the presence of thamnolic acid ('Tham') in a lichen sample in the bi-plot of the redundancy analysis (RDA) of the first and second axes.
Figure 5 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 5 Sample populations of Usnea subfloridana and explanatory variables mean annual air temperature ('Temp') and geographical longitude of populations ('Long') in the bi-plot of the redundancy analysis (RDA) of the first and second axes. The shape of symbols indicates the geographical location of studied populations (square – south-eastern region of mainland, circle - western island and diamond – north-eastern region) and the size of symbols indicates the number of different alleles found in the studied populations.
Figure 2 from: Liu H-M, Shen J-Y, Liang Z-L, Peng F, Wang W-Z, Yang Z-W, Wang S, Parris B, Schneider H (2019) Two out of one: revising the diversity of the epiphytic fern genus Scleroglossum (Polypodiaceae, Grammitidoideae) in southern China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 115-133. https://doi.org/10.3897/phytokeys.130.33979
Figure 2 Reconstruction of the phylogenetic relationships of Scleroglossum species occurring in China including all accessions available in GenBank (October 2018). Newly generated accessions are printed in bold: HaiAcc = Hainan Accessions, two sequences obtained from individual A and B; YunAcc = Yunnan Accessions; VieAcc1 and VieAcc2 = two accessions obtained from the herbaria collections at KUN representing two independent collections (see Suppl. material 1: Table S1). The areas of origin are given for Scleroglossum GenBank accessions. The presented consensus phylogram is based on a Bayesian inference of Phylogeny including 690 accessions represented by rbcL sequences. Clades composed by non-Scleroglossum accessions were pruned. Two stars mark clades with a posterior confidence of p = 1.00 whereas one star marks clade with a posterior confidence p ≥ 0.95 and < 1.00. p.p. = pro parts to indicate the polyphyly of S. sulcatum.
Figure 3 from: Liu H-M, Shen J-Y, Liang Z-L, Peng F, Wang W-Z, Yang Z-W, Wang S, Parris B, Schneider H (2019) Two out of one: revising the diversity of the epiphytic fern genus Scleroglossum (Polypodiaceae, Grammitidoideae) in southern China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 115-133. https://doi.org/10.3897/phytokeys.130.33979
Figure 3 Similarity clustering of the Chinese provinces that are home to at least one grammitid ferns. The clustering analysis was carried out using Jaccard distances and the NJ-tree building algorithm. The underlying scoring (Table 1) was carried out as absence (0) and presence (1).
Figure 1 from: Liu H-M, Shen J-Y, Liang Z-L, Peng F, Wang W-Z, Yang Z-W, Wang S, Parris B, Schneider H (2019) Two out of one: revising the diversity of the epiphytic fern genus Scleroglossum (Polypodiaceae, Grammitidoideae) in southern China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 115-133. https://doi.org/10.3897/phytokeys.130.33979
Figure 1 The grammitid genus Scleroglossum in China. A–EScleroglossum pusillum in Yunnan (YunAcc) and F–HScleroglossum sulcatum in Hainan (HaiAcc). A habitat of S. pusillum occurrences in Yunnan B germinated green spore recovered from opened mature sporangia of S. pusillum. The remains of the spore wall are visible at the lower part of the larger of the two cells that both contain mature chloroplasts. The smaller cell is the first daughter cell formed by the first cell division C habit of S. pusillumD close up of the dorsal surface of the simple leaves showing the location of the submarginal sori and the occurrences of brown branched hairs of S. pusillumE close up of the sorus structure showing the placement at the submargin of the leaves in S. pusillum. F habit of S. sulcatumG close up of the dorsal surface of the simple leaves showing the location of the not submarginal sori and the occurrences of brown branched hairs of S. sulcatumH close up of the sorus structure showing the placement of the sori in dorsal grooves and a distinct lamina margin in S. sulcatum. Scale bars: 0.02 mm (B); 1 mm (E, H).
FIGURE 3 in An unusual new epiphytic species of Cymbidium (Orchidaceae: Epidedroideae) from Hainan, China
FIGURE 3. Seed micromorphology (SEM). A. Cymbidium dayanum. B. Cymbidium lii.
FIGURE 1. A in Colletorichum serranegrense sp. nov., a new endophytic species from the roots of the endangered Brazilian epiphytic orchid Cattleya jongheana
FIGURE 1. A, Cattleya jongheana habitat; B, Flower of C. jongheana.
FIGURE 3 in Verrucaria tenebrosa (Verrucariaceae), a new lichen species from Finland and Norway, and notes on the taxonomy of epiphytic taxa belonging to the V. hydrophila complex
FIGURE 3. Section of perithecium of Verrucaria tenebrosa (holotype).
FIGURE 2 in Verrucaria tenebrosa (Verrucariaceae), a new lichen species from Finland and Norway, and notes on the taxonomy of epiphytic taxa belonging to the V. hydrophila complex
FIGURE 2. Verrucaria tenebrosa (holotype).
Data from: Low modularity and specialization in a commensalistic epiphyte–phorophyte network in a tropical cloud forest
Species interactions can shape the structure of natural communities. Such sets of interactions have been described as complex ecological networks, an example of which is the commensal network formed by epiphyte–phorophyte interactions. Vascular epiphytes germinate and grow on phorophytes (support trees), assuming a horizontal distribution (among the phorophyte species) and a vertical distribution (from the base of the tree trunk to the crown of phorophytes, i.e., through ecological zones). Here we investigated the organization of these structural dimensions of the epiphyte–phorophyte network in a Brazilian tropical montane cloud forest. The analyzed network, comprising 66 epiphyte species and 22 phorophyte species, exhibited a nested structure with a low degree of specialization, a typical pattern for epiphyte–phorophyte networks in forests. The network was slightly modular, with 65% of the species common to three modules, and had vertical structure corresponding to the vertical organization of the phorophytes. The size (diameter at breast height) of phorophyte individuals influenced the network structure, possibly due to the increase in habitat area, the time available for colonization by epiphytes, and a greater number of microenvironments. We found that the distribution of the epiphyte species differed between the phorophyte ecological zones, with greater richness in the lower portions and greater abundance in the upper portions of the phorophytes. The results provide relevant guidance for future research on the characteristics and the vertical and horizontal organization of vascular epiphyte and phorophyte networks.
FIGURE 3 in Patterns of diversity and gaps in vascular (hemi-)epiphyte flora of Southwestern Amazonia
FIGURE 3. Collecting density of epiphytes by municipality in Acre.
FIGURE 4 in Aetokthonos hydrillicola gen. et sp. nov.: Epiphytic cyanobacteria on invasive aquatic plants implicated in Avian Vacuolar Myelinopathy
FIGURE 4. Line drawing showing branching pattern (artist: Bradley Bartelme). Scale = 10 μm.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.