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Figure S14 in Supplementary Materials for Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Figure S14. Phylogeny of Caesalpinioideae. ASTRAL species tree based on the 821 single-copy gene trees. Local posterior probability support values are only shown for nodes with a local posterior probability <1. Branch lengths are expressed in coalescent units. Terminal branches were assigned an arbitrary uniform length for visual clarity.
Fig. 2 in Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Fig. 2. Drivers of phylogenetic turnover of Mimosoid legumes across the global lowland tropics. Bars show relative fractions of phylogenetic turnover explained by predictors (rescaled to add up to one). Numbers above bars are absolute explained percentages of turnover (tables S12 and S20). (A) Phylogenetic turnover explained by climatic distance (maroon), geographic distance (blue), or their interaction (cream). Turnover is assessed across four depths in the phylogeny: with the full metachronogram (age cutoff of 0) and with all clades younger than 5, 10, and 20 Ma collapsed. Note that it was not possible to fit a model to the phylogeny collapsed at 20 Ma for the pantropical and Australian models. (B) Phylogenetic turnover explained by MAP (green) and/or annual mean temperature (orange). Turnover is expressed as phylogenetic turnover not explained by geographic distance ("geographic residuals"). (C) Geographic residuals of phylogenetic turnover explained by MAP (green) and/or precipitation seasonality (gray; left) or dry season length (DSL) (i.e., the number of consecutive months with precipitation <100 mm/month; yellow; right). See fig. S45 for results obtained with an alternative, genus-level Mimosoid phylogeny. P, MAP; T, annual mean temperature; Pseas, precipitation seasonality.
Fig. 1 in Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Fig. 1. Mimosoid evolution and diversity across precipitation gradients. (A) Phylogeny of Mimosoid legumes showing the evolution of precipitation niches and transcontinental dispersal events through time. Branch colors correspond to mean annual precipitation (MAP) estimates [see (C) for scale]. Pie charts at tips and nodes of named clades [sensu (24)] represent observed and estimated spatial distributions [based on area definitions in (D)]. Ancestral niches and areas were estimated using a complete metachronogram for Caesalpinioideae, including non-Mimosoid Caesalpinioideae taxa, but only the Mimosoid clade is shown here. Green circles on branches indicate shifts between precipitation categories [following (17)] that encompass a difference of at least 250-mm MAP; red triangles indicate postulated transcontinental dispersals according to the best-supported model. The six most species-rich genera are labeled. (B) Fractions of niche shifts and transcontinental dispersal events, averaged across multiple optimizations, relative to total phylogenetic splits plotted through time for 5-Ma bins. (E) Mimosoid growth form diversity across the tropical precipitation gradient, from deserts with <50-mm MAP (left) through savannas to rain forests with>5000-mm MAP (right). See the Supplementary Results for species names and photographers. See fig. S51 for more information.
Fig. 37. Scanning electron micrographs for assumed outgroup taxa for Diognetus. A−C 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. 37. Scanning electron micrographs for assumed outgroup taxa for Diognetus. A−C − Argenis incisuratus (Walker, 1873) (from Nakhon Ratchasima, Thailand); D−E − Tinginotopsis sp. (Java, Indonesia); F−L − Tinginotum formosanum Poppius, 1915 (Ryukyus, Japan); M−O − T. perlatum Linnavuori, 1961 (Nagasaki, Japan). A − left lateral habitus; B, G, M − pleura and scent efferent system, left lateral view; C, H − metatarsus; D − anterior body, left lateral view; F − anterior body, dorsal view; I − posterior body, left lateral view; J − sclerotized ring; K, M − posterior wall; L. O − interramal lobe.
Fig. 36 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. 36. Scanning electron micrographs for Diognetus yamato Yasunaga nom. nov. from Shikoku, Japan (A−I), J (A−F) and ♀ (G−I), and immature forms of D. cheimon sp. nov. from Nagasaki, Japan (J−L), D. styrax sp. nov. from Nantou, Taiwan (M−N) and D. vernus sp. nov. from Nagasaki (O). A − anterior body, left lateral view; B − apex of labium with mandibular and maxillary stylets; C − pleura and scent efferent system, left lateral view; D − metatarsus; E, L − pretarsal structure of metaleg; F − apex of pygophore with parameres, left lateral view; G − posterior wall; H − dorsal structure and interramal lobe; I − apex of ovipositor (gonapophysis I); J − 5th instar exuvia, right lateral view; K − 5th instar thorax and abdomen, dorsal view; M − 5th instar nymph, anterior body; N − same, dorsal habitus; O − 5th instar exuvia, dorsal view.
Fig. 35 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. 35. Scanning electron micrographs for Diognetus vernus sp. nov. from southwestern Japan, J (B, G−K) and ♀ (A, C−F, L−O). A – dorsal habitus; B − left lateral habitus; C − anterior body, left lateral view; D − pleura and scent efferent system, left lateral view; E − metatarsus; F − pretarsal structure of metaleg; G−H − apex of pygophore with parameres, left lateral view (G) and dorsal view (H); I − left paramere; J−K − vesica (endosoma); L − sclerotized ring; M − posterior wall; N − dorsal structure; O − interramal lobe.
Fig. 31 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. 31. Scanning electron micrographs for Diognetus laureus sp. nov. from Nagasaki, Japan, J (A−C), ♀ (G−I), 4th instar nymph's exuvia (J−L) and 5th instar's exuvia, J (M−O). A − metatarsi; B − pretarsal structure of metaleg; C − apex of pygophore with parameres, left lateral view; D−E − posterior wall; F − dorsal structure and interramal lobe; G − genital chamber, dorsal view; H − sclerotized ring; I − apex of ovipositor (gonapophysis I); J, M − anterior body, right (J) and left (M) lateral view; K, N − compound eye; L, O − metatarsus.
Fig. 30. Scanning electron micrographs for Diognetus intonsus Distant, 1904 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. 30. Scanning electron micrographs for Diognetus intonsus Distant, 1904, ♀ from Chiang Mai, Thailand (A−I) and D. laureus sp. nov., J from Nagasaki, Japan (J−O). A, K − anterior body, left lateral view; J − left lateral habitus; B, L − scutellum and adjacent structures, left lateral view; C − head and anterior pronotum, dorsal view; D − scutellum and adjacent structures; E−F − metatarsus; G − sclerotized ring; H − posterior wall; I − dorsal structure and interramal lobe; M − dorsal habitus; N − corium; O − posterior corium and anterior cuneus.
Fig. 32 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. 32. Scanning electron micrographs for Diognetus magnificus sp. nov., ♀ from N. Sumatra, Indonesia (A−F) and D. pilosus (Poppius, 1914), ♀ from W. Malaysia (K−M) and Sumatra (G−J, N−P). A − scutellum and adjacent structures, left lateral view; B, I − pleura and scent efferent system, left lateral view; C, J − metatarsus; D, K, N − sclerotized ring; E, O − posterior wall; F, M − interramal lobe; L, P − dorsal structure and interramal lobe.
Fig. 34 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. 34. Scanning electron micrographs for Diognetus puspae sp. nov.,J (A−F), D. schuhorum sp. nov., holotype J (G−I), and D. styrax sp. nov., holotype J (J, L, M−O) and ♀ (K). A, G, J, K − anterior body, left lateral view; B, L − pleura and scent efferent system, left lateral view; C, N − metatarsus; D − left paramere; E − right paramere; F − vesica (endosoma); H − apex of labium; I − apex of pygophore with parameres, left lateral view; M − scutellum and adjacent structures, left lateral view; N − metatarsus; O − pygophore, left lateral view.
Fig. 33 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. 33. Scanning electron micrographs for Diognetus minusculus sp. nov. from Malaysia (except for Sumatra, ♀ on C), J (A−B, D−E, G−K) and ♀ (C−F, L−O). A − dorsal habitus; B–C − left lateral habitus; D − head and anterior pronotum, dorsal view; E − scutellum and adjacent structures, left lateral view; F − pleura and scent efferent system, left lateral view; G − apex of pygophore with parameres, left lateral view; H − mesotarsus (lower) and metatarsus; I − pretarsal structure of metaleg; J − apex of pygophore with parameres, dorsal view; K − vesica; L − genital chamber, dorsal view; M − posterior wall; N − dorsal structure; O − interramal lobe.
Fig. 28 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. 28. Scanning electron micrographs for Diognetus flavigenis (Horváth, 1905) from Honshu, Japan, J (A, C−H) and ♀ (B, K−P). A – left lateral habitus; B − dorsal habitus; C − scutellum and adjacent structures; D − head and pronotum, anterior view; E − pleura and scent efferent system, left lateral view; F − metatarsus; G−H − pretarsal structure of metaleg; I − left paramere; J − right paramere; K − posterior wall; L − dorsal structure; M − dorsal structure and interramal lobe; N − interramal lobe; O − sclerotized ring; P − apex of ovipositor (gonapophysis I).
Fig. 29 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. 29. Scanning electron micrographs for Diognetus insulanus (Yasunaga, 1994) from Okinawa, Japan, J (A, D−E, G−H) and ♀ (B−C, F, I, L−O). A – left lateral habitus; B − dorsal habitus; C − ventral habitus; D − anterior body, left lateral view; E − pleura and scent efferent system, left lateral view; F − metatarsus; G−H − apex of pygophore with parameres, left lateral view (G) and dorsal view (H); I − pretarsal structure of metaleg; J−K − vesica (endosoma); L − posterior wall; M − dorsal structure and interramal lobe; N − sclerotized ring; O − apex of ovipositor (gonapophysis I).
Fig. 27 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. 27. Scanning electron micrographs for Diognetus dhampus sp. nov., J (A−E), D. duwalorum sp. nov., holotype J (F−I), D. giganteus sp. nov., holotype ♀ (J−K) and D. gotohi sp. nov., holotype J (L−O). A, L − anterior body, left lateral view; F, J − left lateral habitus; B, D − scutellum and adjacent structures; C, G, M − pleura and scent efferent system, left lateral view; D, I, N − metatarsus; E, H, O – pygophore.
Fig. 26 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. 26. Scanning electron micrographs for Diognetus cheimon sp. nov. from Nagasaki, Japan,J (A−K) and ♀ (L−P). A−B – left lateral habitus; C − pleura and scent efferent system, left lateral view; D − head and pronotum, left lateral view; D − anterior body, left lateral view; E − metatarsus; F−G − pretarsal structure of metaleg; H − apex of pygophore with exposed vesica and left paramere; I − right paramere; J − left paramere; K − vesica (endosoma); L − sclerotized ring; M − apex of ovipositor (gonapophysis I); N − posterior wall; O − dorsal structure; P − interramal lobe.
Fig. 25 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. 25. Scanning electron micrographs for Diognetus bagmaticus sp. nov. from Nepal, J (A−J) and ♀ (K−O). A−B − dorsal habitus; C − head and anterior pronotum, left lateral view; D − anterior body, left lateral view; E − pleura and scent efferent system, left lateral view; F − pygophore, left lateral view; G − metatarsus; H−I − pretarsal structure of metaleg; J − apex of pygophore with exposed vesica and left paramere; K − genital chamber, dorsal view; L − sclerotized ring; M − posterior wall; N − dorsal structure; O − interramal lobe.
Fig. 16 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. 16. Female genitalia of Diognetus insulanus (Yasunaga, 1994) (A−C), D. intonsus Distant, 1904 (D−E) and D. magnificus sp. nov. (F−H). A, F − genital chamber; D − sclerotized ring; B, G − posterior wall; C, E, H − ovipositor (gonapophysis I). Scale bars 0.1 mm.
Fig. 23. Dorsal vestiture pattern for 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. 23. Dorsal vestiture pattern for 4 Japanese Diognetus species: D. cheimon sp. nov., D. insulanus (Yasunaga, 1994), D. laureus sp. nov and D. vernus sp. nov.
Fig. 19 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. 19. Habitus images of Diognetus spp. A−B − D. schuhorum sp. nov., holotype J, dorsal (A) and ventral (B) views; C−D − D. styrax sp. nov., holotype J; E–F – D. yamato nom. nov., J. Scale bars 2 mm.
Fig. 8 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. 8. Male genitalia of Diognetus bagmaticus sp. nov. (A−D), D. cheimon sp. nov. (E−G), D. dhampus sp. nov. (H−J) and D. duwalorum sp. nov. (K−M). A−B, E − apex of pygophore with parameres; C, H, L − right paramere; I, K − left paramere; D, F−G, J, M − vesica (endosoma). Scale bars 0.2 mm.
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Allen Brain Atlas
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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.
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