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22,710 results for “Plants for planting”
Fig. 12 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 12. Male genitalia of Diognetus gotohi sp. nov. (A−C), D. insulanus (Yasunaga, 1994) (D−F) and D. laureus sp. nov. (G−I). A, D, G − left paramere; B, E, H − right paramere; C, F, I − vesica (endosoma). Scale bars 0.2 mm.
Fig. 5 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 5. Late instar immature forms and eclosion (E−H, L−M) of Diognetus cheimon sp. nov. (A−H) and D. vernus sp. nov. (I−M), observed in Nagasaki, Japan (A, J−K on Eurya japonica and B−C on E. emerginata). A − yellow-green form of 4th (left) and 5th instars; B−C − reddish form of 5th instar; D − 4 anal spots of 5th instar; E − 5th instar nymph (3 hours before eclosion, with pigmented wing-pads); F−H − emerging ♀; I − yellow-green form of 5th instar; J−K − reddish form of 5th instar; L−M − emerging ♀.
Fig. 15 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 15. Male genitalia of Diognetus insulanus (Yasunaga, 1994) (A−E), D. intonsus Distant, 1904 (F−J) and D. magnificus sp. nov. (K−N). A−B, F−G, K−L − left paramere; C, H, M − right paramere; D−E, I−J, N − vesica (endosoma). Scale bars 0.1 mm.
Fig. 24 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 24. Habitus images of most plausible outgroup taxa for Diognetus.A−B − Argenis incisuratus (Walker, 1873) (from Nakhon Ratchasima, Thailand); C − Tinginotum signatum (Distant, 1904) (Rayong, Thailand); D − same, 4th instar nymph; E − final (5th) instar nymph; F − a species similar to T. javanum (Kirkaldy, 1902) (Nakhon Ratchasima, Thailand); G − T. perlatum Linnavuori, 1961 (Nagasaki, Japan).
Fig. 14 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 14. Habitus images of Diognetus spp. A−C − D. insulanus (Yasunaga, 1994), ♀, dorsal (A) and ventral (B) views; C−F − D. intonsus Distant, 1904, J (C) and ♀ (D) from India, ♀ (E−F) from Thailand. G−I – D. magnificus sp. nov., ♀ (G−H) and holotype J (I).
Fig. 18 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 18. Male (A–D) and female (E–G) genitalia of Diognetus minusculus sp. nov. A − left paramere and apex of pygophore; B − right paramere; C−D − vesica (endosoma); E − ovipositor (gonapophysis I); F − genital chamber; G − posterior wall. Scale bars 0.1 mm.
Fig. 1 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 1. Habitats and host plants, Japan (A−F), Nepal (G−H) and Taiwan (I) for Diognetus cheimon sp. nov. (A−F), D. laureus sp. nov. (A−F), D. vernus sp. nov. (A−F), D. bagmaticus sp. nov. (G), D. puspae sp. nov. (H) and D. styrax sp. nov. (I). A–C − Eurya emarginata at preserved wetland (A), house entrance (B) and seaside park (C) in Nagasaki; D − Machilus thunbergii at Satoyama zone in Nagasaki City; E−F − Castanopsis sieboldii at coastal zones in Nagasaki City; G − Quercus semecaprifolia, inflorescence, at Nagarjun, Kathmandu; H − flowers of Schima wallichii at Godawari Valley, Lalitpur; I − Styrax formosanus, flowers, in Nantou.
Fig. 4 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 4. Habitus images of Diognetus cheimon sp. nov. (all from Nagasaki, Japan).A − J sucking on Eurya emarginata fruit; B − 5th instar nymph (left) and J on flower buds of Eurya japonica; C − ♀; D − J (left) and ♀ sucking on young fruits of E. japonica; E−F − ventral habitus images of J (E) and ♀ (F).
Fig. 21 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 21. Male genitalia of Diognetus styrax sp. nov. (A−C), D. vernus sp. nov. (D−G) and D. yamato nom. nov. (H−J). A, D, H − left paramere; B, E, I − right paramere; C, F−G, J − vesica (endosoma). Scale bars 0.2 mm.
Fig 13 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig 13. Habitus images of adults (A−E) and immature forms (F−I) for Diognetus laureus sp. nov. A, C − male on Machilus thunbergii (C− holotype); B, E − female; D − male and exuvia (left); F − 4th instar nymph; G − 3rd (left) and 5th instar nymphs; H−I − 5th instar nymph.
Fig. 7 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 7. Habitus images of Diognetus spp. A−C − D. bagmaticus sp. nov., J (A−B) and ♀ (C); D – undetermined J specimen from Queensland, Australia; E−F − D. dhampus sp. nov., J; G−H − D. duwalorum sp. nov., holotype J; I − D. giganteus sp. nov., holotype ♀; J−K − D. gotohi sp. nov., holotype J; L−N − D. flavigenis (Horváth, 1905), J (M − head in frontal view). Scale bar 2 mm.
Fig. 22 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 22. Female genitalia of Diognetus pilosus (Poppius, 1914) (A–B – 00419636 from Sumatra, C–D – from Malaysia), D. styrax sp. nov. (E−F), D. vernus sp. nov. (G−I) and D. yamato nom. nov.(J−L). A, C, H, K − genital chamber. B, D, E, G, J − posterior wall; F, I, L − ovipositor (gonapophysis I); Scale bars 0.1 mm.
Fig. 17 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 17. Habitus images of Diognetus spp. A−C − D. minusculus sp. nov., J (A) and ♀ (B−C); D−E − D. pilosus, J (D) and ♀ (E); F − D. puspae sp. nov., J. Scale bar 2 mm.
Fig. 3. Habitus images for Diognetus species from Japan and Taiwan. A–B – D in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 3. Habitus images for Diognetus species from Japan and Taiwan. A–B – D. flavigenis (Horváth, 1905) (from Kumano, Wakayama), C – D. insulanus (Yasunaga, 1994) (from Okinawa), D–F – D. styrax sp. nov., ♀ (D–E) and 5th instar nymph (Nantou, Taiwan), G–H – D. yamato nom. nov. (from Kochi).
Fig. 20 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 20. Male genitalia of Diognetus puspae sp. nov. (A−C) and D. schuhorum sp. nov. (D−F). A, E − left paramere; B, E − right paramere; C, F − vesica (endosoma). Scale bars 0.2 mm.
Fig. 6 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 6. Habitus images of Diognetus vernus sp. nov. (all from Nagasaki, Japan). A − holotype J; B − ♀; C − ♀ darkened variant; D − newly emerged ♀ (left) and J; E−F − ventral habitus images of J (E) and ♀ (F).
Fig. 9 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 9. Female genitalia of Diognetus bagmaticus sp. nov. (A−B) and D. intonsus Distant, 1904 (C−D). A, C − posterior wall; B, D − genital chamber. Scale bars 0.1 mm.
Fig. 10 in Revision of the plant bug genus Diognetus, with descriptions of thirteen new species from the Oriental and Eastern Palearctic Regions (Hemiptera: Heteroptera: Miridae)
Fig. 10. Female genitalia of Diognetus bagmaticus sp. nov. (A−D), D. cheimon sp. nov. (E−G) and D. laureus sp. nov. (H−K). A, E − genital chamber; B, I − sclerotized ring; C, F, J − posterior wall; D, G, K − ovipositor (gonapophysis I). Scale bars 0.1 mm.
Data for: Single-gene resolution of diversity-driven overyielding in plant genotype mixtures
<p>In plant communities, diversity often increases productivity and functioning, but the specific underlying drivers are difficult to identify. Most ecological theories attribute positive diversity effects to complementary niches occupied by different species or genotypes. However, the specific nature of niche complementarity often remains unclear, including how it is expressed in terms of trait differences between plants. Here, we use a gene-centred approach to study positive diversity effects in mixtures of natural <em>Arabidopsis </em><em>thaliana</em> genotypes. Using two orthogonal genetic mapping approaches, we find that between-plant allelic differences at the <em>AtSUC8</em> locus are strongly associated with mixture overyielding. <em>AtSUC8</em> encodes a proton-sucrose symporter and is expressed in root tissues. Genetic variation in <em>AtSUC8</em> affects the biochemical activities of protein variants and natural variation at this locus is associated with different sensitivities of root growth to changes in substrate pH. We thus speculate that - in the particular case studied here - evolutionary divergence along an edaphic gradient resulted in the niche complementarity between genotypes that now drives overyielding in mixtures. Identifying such genes important for ecosystem functioning may ultimately allow linking ecological processes to evolutionary drivers, help identify traits underlying positive diversity effects, and facilitate the development of high-performing crop variety mixtures.</p>
Plants metacommunity from temporary ponds
<p>The database comprises a long-term survey of a plant metacommunity of temporary ponds. The metacommunity is <span><span>located in a flat landscape surrounded by hills, where a maximum of 61 ponds, every year</span><span>,</span><span> are filled with water in winter and dry out in summer in the same spatial locations. Information on species occurrences at the sampling unit level was recorded since 2005 (until 2022 and continuous). </span></span></p> <p><span>The database includes: </span></p> <ol> <li><span>Species occurrences at the sampling unit level for 61 temporary ponds along 14 years (to be periodically updated). </span></li> <li><span>Species traits database and functional description of traits. </span></li> <li><span>Environmental information of each pond including connectivity, area, heterogeneity and hydroperiod.</span></li> </ol>
ScienceDex guides
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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.