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1,808 results for “flower plantings”
Lamium amplexicaule (Lamiaceae) - whole plant - in flower - general view
Image of Lamium amplexicaule (Lamiaceae) - whole plant - in flower - general view
Corydalis flavula (Fumariaceae) - whole plant - in flower - general view
Image of Corydalis flavula (Fumariaceae) - whole plant - in flower - general view
Claytonia virginica (Portulacaceae) - whole plant - in flower - general view
Image of Claytonia virginica (Portulacaceae) - whole plant - in flower - general view
Mertensia virginica (Boraginaceae) - whole plant - in flower - general view
Image of Mertensia virginica (Boraginaceae) - whole plant - in flower - general view
Fig. 4. A–J in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 4. A–J. Habitus of males of Ebenacobius Haran gen. nov. in lateral view (part 1). A. E. curvisetis Haran gen. et sp. nov. B. E. thoracicus Haran gen. et sp. nov. C. E. rectirostris Haran gen. et sp. nov. D. E. xhosa Haran gen. et sp. nov. E. E. duplicatus Haran gen. et sp. nov. F. E. san Haran gen. et sp. nov. G. E. grobbelaarae Haran gen. et sp. nov. H. E. kuscheli Haran gen. et sp. nov. I. E. costalis (Fåhraeus, 1844) gen. et comb. nov. J. E. mulanjensis Haran gen. et sp. nov. A–J = not to scale.
Fig. 8 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 8. Best-fit ML tree of Ebenacobius Haran gen. nov. and Afrotropical Derelomini resulting from the partitioned analyses of the concatenated molecular dataset (the scale bar represents the estimated number of nucleotide substitutions per site). Support values (*) at nodes indicate SH-aLRT ≥ 80% and uBV ≥ 95% values, in that order.
Fig. 7 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 7. Habitus in natura, host plants and habitats of Ebenacobius Haran gen. nov. A. Habitus of adult of E. rectirostris Haran gen. et sp. nov. B. Inflorescence of Euclea natalensis A.DC. (Ebenaceae), host of E. rectirostris. C. Biotope of E. rectirostris in the Mpumalanga Province of South Africa. D. Habitus of adult of E. san Haran gen. et sp. nov. E. Inflorescence of Euclea racemosa L. (Ebenaceae), host of E. san. F. Biotope of E. san in the Western Cape Province of South Africa.
Fig. 2. A–I in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 2. A–I. Habitus of males of Ebenacobius Haran gen. nov. in dorsal view (part 1). A. E. curvisetis Haran gen. et sp. nov. B. E. rectirostris Haran gen. et sp. nov. C. E. duplicatus Haran gen. et sp. nov. D. E. grobbelaarae Haran gen. et sp. nov. E. E. costalis (Fåhraeus, 1844) gen. et comb. nov. F. E. thoracicus Haran gen. et sp. nov. G. E. xhosa Haran gen. et sp. nov. H. E. san Haran gen. et sp. nov. I. E. kuscheli Haran gen. et sp. nov. Scale bars = 1 mm.
Fig. 5. A–H in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 5. A–H. Habitus of males of Ebenacobius Haran gen. nov. in lateral view (part 2). A. E. hessei Haran gen. et sp. nov. B. E. incognitus (Hesse, 1929) gen. et comb. nov. C. E. pedi Haran gen. et sp. nov. D. E. oberprieleri Haran gen. et sp. nov. E. E. tsonga Haran gen. et sp. nov. F. E. turneri (Marshall, 1935) gen. et comb. nov. G. E. hippopotamorum Haran gen. et sp. nov. H. E. rhodesianus (Hesse, 1929) gen. et comb. nov. A–H = not to scale.
Fig. 1 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 1 (see preceding page). A–M. Details of morphology and measurements of Ebenacobius Haran gen. nov. and Derelomus Schoenherr, 1825. A. Ebenacobius rhodesianus (Hesse, 1929) gen. et comb. nov. in dorsal view, with the white arrows showing where the measurements of width (w) and length (L) are made for the prothorax (top) and elytra (bottom). Black arrow showing the narrowing of prothorax near apical margin. B. Head in lateral view of E. rhodesianus with white arrow showing the groove on forehead and the black arrow showing the convexity of the eyes, exceeding the lateral curve of head. C. Head and apex of prothorax in dorsal view of Derelomus chamaeropsis Fabricius, 1798 with the white arrow showing flat forehead, lacking groove and black arrow showing the constriction on the prothorax near apical margin. D. Detail of the top-left part of the right elytron in E. rhodesianus showing the white scales on interstriae and with the well aligned punctures at base of stria 1 highlighted in white. E. Detail of the top-left part of the right elytron in E. costalis (Fåhraeus, 1844) gen. et comb. nov. showing the setae on interstriae and with the misaligned punctures at base of stria 1 highlighted in white. F. Protibia of males of E. rhodesianus, showing the apical acute mucro and the ante-apical brush of setae. G. Head and prothorax of E. rhodesianus in lateral view with the arrows showing where measurements of rostrum and prothorax length are made. H. Right maxilla of E. rhodesianus in dorsal view. I. Penis of E. costalis in dorsal view showing were measurements are made for the body of penis (white arrows: width; top right black arrows: length) and the length of apodemes (bottom right black arrows). J. Stridulatory plate (tergite VII) in male of E. rhodesianus in dorsal view, with the cuticular tubercles used for stridulation highlighted in white. K–M. Female genitalia. K. Ovipositor in E. rhodesianus. L. Sternite VIII, same species. M. Spermatheca, same species. N. Right mandible, same species. O. Labial prementum, same species. A–O: not to scale.
Fig. 6 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 6 (part 1). A–I. Male genitalia of Ebenacobius Haran gen. nov., penis in dorsal (left) and lateral (right) view.A. E. curvisetis Haran gen. et sp. nov. B. E. rectirostris Haran gen. et sp. nov. C. E. duplicatus Haran gen. et sp. nov. D. E. grobbelaarae Haran gen. et sp. nov. E. E. costalis (Fåhraeus, 1844) gen. et comb. nov. F. E. thoracicus Haran gen. et sp. nov. G. E. xhosa Haran gen. et sp. nov. H. E. san Haran gen. et sp. nov. I. E. kuscheli Haran gen. et sp. nov. A–I = not to scale.
Fig. 6 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 6 (part 2). J–R. Male genitalia of Ebenacobius Haran gen. nov.. penis in dorsal (left) and lateral (right) view. J. E. mulanjensis Haran gen. et sp. nov. K. E. hessei Haran gen. et sp. nov. L. E. pedi Haran gen. et sp. nov. M. E. tsonga Haran gen. et sp. nov. N. E. hippopotamorum Haran gen. et sp. nov. O. E. incognitus (Hesse, 1929) gen. et comb. nov. P. E. oberprieleri Haran gen. et sp. nov. Q. E. turneri (Marshall, 1935) gen. et comb. nov. R. E. rhodesianus (Hesse, 1929) gen. et comb. nov. J–R = not to scale.
Selection against early flowering in geothermally heated soils is associated with pollen but not prey availability in a carnivorous plant
<p>This data set includes data on flowering phenology, rosette diameters and fitness of the perennial herb Pinguicula vulgaris, as well as data on soil temperature and experimental treatment applied. The data was collected during the summer of 2020 in 287 plant individuals located in a sub-arctic geothermal area in Ölfus municipality in SW-Iceland, Hengill (64°03’N; 21°18’W, ~360 m.a.s.l.).</p>
Nectar values from: Quantifying nectar production by flowering plants in urban and rural landscapes
<p>Floral resources (nectar and pollen) provide food for insect pollinators but have declined in the countryside due to land use change. Given widespread pollinator loss, it is important that we quantify their food supply to help develop conservation actions. While nectar resources have been measured in rural landscapes, equivalent data are lacking for urban areas, an important knowledge gap as towns and cities often host diverse pollinator populations.</p> <p>We quantified the nectar supply of urban areas, farmland and nature reserves in the UK by combining floral abundance and nectar sugar production data for 536 flowering plant taxa, allowing us to compare landscape types and assess the spatial distribution of nectar sugar among land uses within cities.</p> <p>The magnitude of nectar sugar production did not differ significantly among the three landscapes. In urban areas the nectar supply was more diverse in origin and predominantly delivered by non-native flowering plants. Within cities, urban land uses varied greatly in nectar sugar production. Gardens provided the most nectar sugar per unit area and 85% of all nectar at a city scale, while gardens and allotments produced the most diverse supplies of nectar sugar. Floral abundance, commonly used as a proxy for pollinators' food supply, correlated strongly with nectar resources, but left a substantial proportion of the variation in nectar supply unexplained.</p> <p>Synthesis. We show that urban areas are hotspots of floral resource diversity rather than quantity and their nectar supply is underpinned by the contribution of residential gardens. Individual gardeners have an important role to play in pollinator conservation as ornamental plants, usually non-native in origin, are a key source of nectar in towns and cities.</p>
Text-fig. 9. The drawing shows the ratio of epigynous and hypogenous flowers in Zliv-Řídká Blana mesofossil flora. The ovary is inferior, and the flower is epigynous in 17 taxa. The ovary is superior, and the flower is hypogenous in 20 taxa. in Plant Mesofossils From The Late Cretaceous Klikov Formation, The Czech Republic
Text-fig. 9. The drawing shows the ratio of epigynous and hypogenous flowers in Zliv-Řídká Blana mesofossil flora. The ovary is inferior, and the flower is epigynous in 17 taxa. The ovary is superior, and the flower is hypogenous in 20 taxa.
Text-fig. 8. Scanning electron micrographs (a–f, h) and X-ray microtomographic orthoslices (g) of flowers from Zliv-Řídká Blana locality. a: Taxon 27, epigynous flower, no. NM-F 4504; b: Taxon 30, epigynous flower, remains of two thick sepals, a massive nectary disk (arrowhead) and two styles, no. NM-F 3199; c: Taxon 29, flower with stamens have long filament, calyx (ca) and corolla (co), no. NM-F 3198; d: Taxon 32, flower, no. NM-F 4503; e–h: Taxon 14, e – hypogenous flower, no. NM-F 3196, f – floral bud with a thick pedicel, no. NM-F 3196, g – flower with gynoecium showing central placentation and several seeds, no. NMF 3196, h – flower with gynoecium showing several seeds, no. NM-F 4505. in Plant Mesofossils From The Late Cretaceous Klikov Formation, The Czech Republic
Text-fig. 8. Scanning electron micrographs (a–f, h) and X-ray microtomographic orthoslices (g) of flowers from Zliv-Řídká Blana locality. a: Taxon 27, epigynous flower, no. NM-F 4504; b: Taxon 30, epigynous flower, remains of two thick sepals, a massive nectary disk (arrowhead) and two styles, no. NM-F 3199; c: Taxon 29, flower with stamens have long filament, calyx (ca) and corolla (co), no. NM-F 3198; d: Taxon 32, flower, no. NM-F 4503; e–h: Taxon 14, e – hypogenous flower, no. NM-F 3196, f – floral bud with a thick pedicel, no. NM-F 3196, g – flower with gynoecium showing central placentation and several seeds, no. NMF 3196, h – flower with gynoecium showing several seeds, no. NM-F 4505.
Text-fig. 3. Scanning electron micrographs of Normapolles flowers/fruits from Zliv-Řídká Blana locality. a: Budvaricarpus serialis, aggregation of laterally fused fruits supported by a common bract (br – bract, hp – hypanthium), no. NM-F 3160; b: Budvaricarpus sp., aggregation of laterally fused fruits supported by several bracts, no. NM-F 3619; c: Caryanthus trebecnsis, reproductive unit consists of three bisexual, epigynous flowers/young fruits, no. NM-F 3286; d: Dahlergeniantus sp., hypogynous flower with radial symmetry, no. NM-F 4495; e: Calathiocarpus sp., epigynous flower with radial symmetry, no. NM-F 4631; f: Caryanthus sp. 1, ribbed fruit–nut of deltoid shape, no. NM-F 3208; g: Zlivifructus vachae, bisymmetrical flower with four tepals and four stamens, no. NM-F 3172; h: Taxon 3, ribbed fruit of Normapolles affinity, no. NM-F 3724. in Plant Mesofossils From The Late Cretaceous Klikov Formation, The Czech Republic
Text-fig. 3. Scanning electron micrographs of Normapolles flowers/fruits from Zliv-Řídká Blana locality. a: Budvaricarpus serialis, aggregation of laterally fused fruits supported by a common bract (br – bract, hp – hypanthium), no. NM-F 3160; b: Budvaricarpus sp., aggregation of laterally fused fruits supported by several bracts, no. NM-F 3619; c: Caryanthus trebecnsis, reproductive unit consists of three bisexual, epigynous flowers/young fruits, no. NM-F 3286; d: Dahlergeniantus sp., hypogynous flower with radial symmetry, no. NM-F 4495; e: Calathiocarpus sp., epigynous flower with radial symmetry, no. NM-F 4631; f: Caryanthus sp. 1, ribbed fruit–nut of deltoid shape, no. NM-F 3208; g: Zlivifructus vachae, bisymmetrical flower with four tepals and four stamens, no. NM-F 3172; h: Taxon 3, ribbed fruit of Normapolles affinity, no. NM-F 3724.
Xyris tennesseensis (Xyridaceae) - herbaceous angiosperms - whole plant - in flower - general view
Image of Xyris tennesseensis (Xyridaceae) - herbaceous angiosperms - whole plant - in flower - general view
Xyris tennesseensis (Xyridaceae) - herbaceous angiosperms - whole plant - in flower - general view
Image of Xyris tennesseensis (Xyridaceae) - herbaceous angiosperms - whole plant - in flower - general view
Xyris tennesseensis (Xyridaceae) - herbaceous angiosperms - whole plant - in flower - general view
Image of Xyris tennesseensis (Xyridaceae) - herbaceous angiosperms - whole plant - in flower - general view
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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.