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96 results for “epiphytic species”
Fig. 10 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 10. Chaetonotus (Chaetonotus) invitatus sp. nov. Detail of internal morphology. Bright field microphotography. X-organ.
Fig. 13 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 13. Chaetonotus (Chaetonotus) paucisquamatus Kisielewski, 1991. Adult specimen. Bright field microphotographs. A. Anterior trunk, dorsal view. B. Anterior trunk ventral view. C. Posterior trunk dorsal view. D. Posterior trunk, ventral view.
Fig. 9 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 9. Chaetonotus (Chaetonotus) invitatus sp. nov. Adult specimen. Bright field microphotographs. A. Detail of the mouth ring, dorsal view. B. Detail of the mouth ring, internal view. C. Detail of the pharynx.
Fig. 25 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 25. Chaetonotus (Hystricochaetonotus) horridus sp. nov. Detail of the internal morphology. Bright field microphotographs. A. Mature egg. B. Sperm pocket. C. X-organ and sperm pocket.
Fig. 7 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 7. Chaetonotus (Chaetonotus) invitatus sp. nov. Bright field microphotographs. A. Detail of dorsal head view of adult specimen. B. Detail of dorsal head view of juvenile specimen. C. Dorsal view of posterior trunk region of specimen with two scales 17. D. Dorsal view of posterior trunk region of specimen with three scales 17.
Fig. 34 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 34. Chaetonotus (Zonochaeta) cestacanthus Balsamo, 1990. Adult specimen. A. Habitus, phase contrast microphotograph. B. Posterior trunk region, furca base and furcal appendages, dorsal view, phase contrast microphotograph. C. Posterior trunk region, furca base and furcal appendages, dorsal view, bright field microphotograph.
Fig. 27 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 27. Chaetonotus (Hystricochaetonotus) inaequabilis sp. nov. Schematic drawings of the scales. A. Head anteriormost scale (scale 1). B. Head anteriormost central scale (scale 2). C. Anterior head dorsal scale (scale 3). D. Anterior head dorsolateral and lateral scale (scale 4). E. Anterior head ventrolateral scale (scale 5). F. Head ventral scale (scale 6). G. Posterior head dorsal scale (scale 7). H. Posterior head dorsolateral and lateral scale (scale 8). I. Posterior head ventrolateral scale (scale 9). J. Anterior neck dorsal scale (scale 10). K. Neck dorsolateral and lateral scale (scale 11). L. Neck ventrolateral scale (scale 12). M. Neck ventral scale (scale 13). N. Posterior neck dorsal scale (scale 14). O. Anterior trunk dorsal, dorsolateral, lateral and ventrolateral scale (scale 15). P. Trunk ventral scale (scale 16). Q. Posterior trunk dorsal, dorsolateral, lateral and ventrolateral scale (scale 17). R. Scale 18. S. Scale 19. T. Scale 20. U. Scale 21. V. Scale 22. W. Scale 23. X. Scale 24. Y. Scale 25. Z. Scale 26. AA. Scale 27. BB. Scale 28. CC. Scale 29. DD. Scale 30. EE. Scale 31. FF. Scale 32. GG. Scale 33.
Fig. 8 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 8. Chaetonotus (Chaetonotus) invitatus sp. nov. Bright field microphotographs. A. Dorsal view of the posterior trunk region, furca base and furcal appendage scales. B. Ventral view of the posterior trunk region, furca base and furcal appendage scales.
Fig. 33 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 33. Chaetonotus (Zonochaeta) cestacanthus Balsamo, 1990. Adult specimen. Bright field microphotographs. A. Scales and spines, dorsal view. B. Scales and spines, ventral view.
Fig. 6 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 6. Chaetonotus (Chaetonotus) invitatus sp. nov. Bright field microphotographs. A. Head, dorsal view. B. Head, ventral view. C. Neck, dorsal view. D. Neck, ventral view. E. Trunk, dorsal view. F. Trunk, ventral view. G. Furca base and furcal appendages, dorsal view. H. Furca base and furcal appendages, ventral view.
Fig. 5 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 5. Chaetonotus (Chaetonotus) invitatus sp. nov. Habitus. Phase contrast microphotographs. A. Juvenile specimen. B. Adult specimen. C. Specimen with mature egg.
Fig. 3 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 3. Chaetonotus (Chaetonotus) invitatus sp. nov. Schematic drawings of the scales. A. Head anteriormost dorsal scale (scale 1). B. Head dorsal scale (scale 2). C. Head dorsolateral scale (scale 3). D. Head lateral and ventrolateral scale (scale 4). E. Head ventral scale (scale 5). F. Anterior neck dorsal scale (scale 6). G. Anterior neck dorsolateral scale (scale 7). H. Anterior neck lateral and ventrolateral scale (scale 8). I. Anterior neck ventral scale (scale 9). J. Posterior neck dorsal scale (scale 10). K. Posterior neck dorsolateral scale (scale 11). L. Posterior neck lateral and ventrolateral scale (scale 12). M. Posterior neck ventral scale (scale 13). N. Trunk dorsal scale (scale 14). O. Trunk dorsolateral scale (scale 15). P. Trunk lateral and ventrolateral scale (scale 16). Q. Trunk ventral scale (scale 17). R. Scale 18. S. Scale 19. T. Scale 20. U. Scale 21. V. Scale 22. W. Scale 23. X. Scale 24. Y. Scale 25. Z. Scale 26. AA. Scale 27. BB. Scale 28. CC. Scale 29. DD. Scale 30. EE. Scale 31. FF. Scale 32. GG. Scale 33. HH. Scale 34. II. Scale 35.
Fig. 2 in Gastrotricha - not only in sediments: new epiphytic species of Chaetonotida from the Jubilee Greenhouse of the Botanical Garden in Kraków
Fig. 2. Chaetonotus (Chaetonotus) invitatus sp. nov. Schematic drawings. A. Dorsal body view. B. View of internal morphology. C. Ventral body view. Light grey areas indicate the areas of the insertion of ciliary bands.
Fig 1. — Eulophia epiphytica. A in An unusual new epiphytic species of Eulophia (Orchidaceae) from southeastern Madagascar
Fig 1. — Eulophia epiphytica. A, habit; B, C, flower, front and dorsal views; D, flower side view with nearmost lateral sepal and petal removed; E, dorsal sepal; F, lateral sepal; G, petal; H, lip; I, column, ovary and bract; J, column ventral view; K, column apex with anther hinged back; L, anther and pollinia; M, habit on Elaeis guineensis; N, pollinia. All drawn by Olivier WHALLEY from the type collection.
Plant size and leaf traits for epiphyte species found in flooded gallery forests and non-flooded gallery forests in Central Brazil
<p>Despite their unique adaptations to thrive in canopy environments without access to soil resources, epiphytes are underrepresented in studies of functional traits and of functional composition of tropical plant communities. We investigated functional traits of spermatophytic (seed-bearing) C<sub>3</sub> and CAM epihyte communities in flooded and non-flooded gallery forests in Central Brazil. The two forest types differ in floristic, structure, microclimate and edaphic conditions. We studied plant size, leaf thickness, leaf dry matter content, leaf area, specific leaf area, leaf C, N, P, K, Mg, Ca and C and N stable isotope ratios. Because photosynthetic pathway (C<sub>3</sub> or CAM) is an important aspect of ecologial differentiation of spermatophytic epiphytes, we expected that functional trait syndromes in a multivariate space would be more associated with photosynthetic pathway than forest type and changes in abundance of C<sub>3</sub> and CAM epiphytes would drive functional trait composition at the community level. C<sub>3</sub> and CAM epiphytes segregated in the multivariate trait space, however more complex functional typologies were also evident. Despite lower light levels, CAM epiphytes were more abundant in the flooded gallery forest. There, they accounted for 80% of all individuals, whereas C<sub>3</sub> epiphytes dominated in the non-flooded forest. These large differences in the proportion of C<sub>3</sub> and CAM epiphytes strongly affected functional trait values at the community level, despite very little intraspecfic variation in trait values between forest types for species that occurred in both forests. </p>
Data from: Orchid trade at the source: Epiphytic species with conspicuous flowers in low-elevation forests are more locally collected in a Philippine key biodiversity area
<p>Orchids are the most heavily traded plant group globally, putting pressure on wild populations in many source countries like the Philippines. Despite its rich orchid diversity, there remains a notable gap in understanding the factors driving orchid trade within the country. To address this knowledge gap and support orchid conservation efforts, we utilized a five-year orchid diversity dataset extensively collected through floristic field and village garden surveys in one of the largest key biodiversity areas in the southern Philippines. We employed a trait-based approach to investigate ecological drivers of local orchid collection within this source area. Our results show that around 36% of local orchid diversity have predicted collection risks of ≥50%. Notably, locally collected orchid species exhibited multiple, large, and conspicuously colored flowers that are found in low-elevation forests and higher up in forest stratum. Elevational distribution and flower size emerged as the strongest predictors, potentially influencing collection preferences. Our analysis of predicted collection risks underscores the vulnerability of both threatened and non-threatened orchid species to local collection pressures. Moreover, we highlight the practical utility of our trait-based approach in predicting risks and informing management strategies for local orchid conservation. This research marks a significant step towards identifying ecological drivers influencing orchid trade at its source, providing insights that can inform targeted conservation strategies across many key biodiversity areas for this highly diverse, charismatic, and threatened plant family.</p>
Vertical variation in epiphytic cryptogam species richness and composition in a primeval Fagus sylvatica forest
<p>"Data description.docx " contains the description of the data-file " Data_JVS_Vertical variation.xlsx" used for analyses.<br> </p>
Data from: Orchid trade at the source: Epiphytic species with conspicuous flowers in low-elevation forests are more locally collected in a Philippine key biodiversity area
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Data from: Effects of microclimates on species richness of epiphytic and non-epiphytic bryophytes along a subtropical elevational gradient in China
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Data from: Ghost species form an important component of the epiphytic biota in temperate forests
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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.