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FIGURE 4. Magnolia unicarmensis. A. Leaf. B. Twig. C in Magnolia unicarmensis (Magnolia subsect. Dugandiodendron; Magnoliaceae): a new species from tropical montane forests of Antioquia, Colombia
FIGURE 4. Magnolia unicarmensis. A. Leaf. B. Twig. C. Leaves and stipules in the treetop. D and E. Fruit. Photos by A.F. MontoyaLópez.
FIG. 1. Siphocampylus flavescens. A. Habit. B. Flowering branch. C. Adaxial leaf surface. D. Abaxial leaf surface. E in Siphocampylus flavescens (Campanulaceae, Lobelioideae), a New Endangered Species from Southeastern Brazil
FIG. 1. Siphocampylus flavescens. A. Habit. B. Flowering branch. C. Adaxial leaf surface. D. Abaxial leaf surface. E. Detail of an immature fruit. F. Detail of a flower. Photographs by Guilherme Peres Coelho.
CO2 Electroreduction To Syngas With Tunable Composition In An Artificial Leaf
<p>Experimental dataset corresponding to figures in the main manuscript and supporting information</p>
FIGURE 6. Magnolia cirorum. A, B, D. Leaf variability. C, E, F in Magnolia cirorum (Magnolia sect. Talauma, Magnoliaceae), a new species from Pico Bonito National Park, Atlántida, Honduras
FIGURE 6. Magnolia cirorum. A, B, D. Leaf variability. C, E, F. Gynoecium and stamens at male-phase. G. Sepals and petals. H. Immature seeds. I, J Mature seeds. K. Scarified seeds with a black seed coat. Photographs A & H–K by A.H. Martínez; and B–G by A. Vázquez.
FIGURE 3. Pathogenicity test results for C in Eucalyptus leaf spot disease caused by Coniella eucalyptorum in Sri Lanka
FIGURE 3. Pathogenicity test results for C. eucalyptorum on E. camaldulensis leaves. a1–a4 wounded leaves inoculated with C. eucalyptorum spore suspensions. b1–b2 non-wounded leaves inoculated with C. eucalyptorum spore suspensions. c1–c2 non-wounded leaves inoculated with sterile water (control). d1–d2 wounded leaves inoculated with sterile water (control). e1–e4 wounded leaves inoculated with C. eucalyptorum mycelial plugs. f1–f2 non-wounded leaves inoculated with C. eucalyptorum mycelial plugs. g1–g2 wounded leaves inoculated with sterile PDA plugs (control). h1–h2 non-wounded leaves inoculated with sterile PDA plugs (control).
FIGURE 1 in Eucalyptus leaf spot disease caused by Coniella eucalyptorum in Sri Lanka
FIGURE 1. Phylogram generated for Coniella species from ML and BI analyses based on a combined dataset of ITS, LSU, and tef1-α sequences. The tree is rooted with Melanconiella sp. (CBS110385). Bootstrap support values for ML ≥ 65 % and Bayesian posterior probabilities (PP) ≥ 0.95 are shown at the nodes. The strain from the current study is in red. All ex-type strains are in bold black. Some branches were shortened to fit them to the pages, and these are indicated by two diagonal lines with the number of times a branch was shortened indicated next to the lines.
FIGURES 107–115 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 107–115. Teuchothrips of Australia. T. tolga 107–112: (107) head & pronotum; (108) antenna; (109) prosternites; (110) tergites IX–X; (111) pelta of female; (112) pelta of male. T. toowoomba 113–115: (113) head; (114) pronotum; (115) metanotum and pelta.
FIGURES 96–106 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 96–106. Teuchothrips of Australia. T. simplicipennis 96–101: (96) head & pronotum; (97) antenna; (98) metanotum & pelta; (99) prosternites; (100) male sternite VIII; (101) tergites IX–X. (102) T. sodalis metanotum. T. soror 103–106: (103) head; (104) antenna; (105) metanotum & pelta; (106) prosternites.
FIGURES 88–95 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 88–95. Teuchothrips of Australia. T. miriwoong 88–90: (88) head & pronotum; (89) antenna; (90) metanotum & pelta. T. monga 91–92: (91) metanotum & pelta; (92) pronotum. T. mooni 93–95: (93) head & pronotum; (94) metanotum & pelta; (95) tergites IX–X.
FIGURES 76–87 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 76–87. Teuchothrips of Australia. T. mareeba 76–80: (76) head & pronotum; (77) metanotum & pelta; (78) prosternites; (79) tergites IX–X; (80) fore wing sub-basal setae. T. melaleucae 81–83: (81) metanotum & pelta; (82) antenna; (83) head & pronotum. T. minor 84–87: (84) head & pronotum; (85) metanotum & pelta; (86) antenna; (87) fore wing sub-basal setae.
FIGURES 63–75 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 63–75. Teuchothrips of Australia. T. larrakia 63–64: (63) head & pronotum; (64) fore tarsus, male. T. leptospermum 65–67: (65) head & pronotum; (66) metanotum & pelta; (67) antenna. T. longiseta 68–70: (68) head & pronotum; (69) type slide; (70) metanotum & pelta. T. lutruwita 71–75: (71) antenna; (72) head; (73) metanotum & pelta; (74) prosternites; (75) tergites IX–X.
FIGURES 44–52 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 44–52. Teuchothrips of Australia. T. jarowair 44–48: (44) head; (45) pronotum; (46) metanotum & pelta; (47) tergites IX–X; (48) male sternite VIII. T. jukun 49–52: (49) head & pronotum; (50) fore tarsus; (51) metanotum & pelta; (52) tergite VIII, male.
FIGURES 53–62 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 53–62. Teuchothrips of Australia. T. kaurna 53–55: (53) head, thorax & pelta; (54) antenna; (55) tergites IX–X. T. kokatha 56–62: (56) head; (57) head & pronotum; (58) metanotum & pelta; (59) pronotum; (60) antenna; (61) metanotum; (62) pelta.
FIGURES 27–36 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 27–36. Teuchothrips of Australia. (27) T. clavipilus head. T. connatus 28–30: (28) head & pronotum anterior margin; (29) antenna; (30) metanotum & pelta. T. disjunctus (31) head. T. dodonaea 32–34: (32) head & pronotum; (33) antenna; (34) metanotum & pelta. T. froggatti 35–36: (35) head & pronotum; (36) metanotum & pelta.
FIGURES 11–26 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 11–26. Teuchothrips of Australia. T. badiipennis 11–12: (11) metanotum & pelta; (12) prosternites. T. badu 13– 16: (13) head & pronotum; (14) metanotum & pelta; (15) prosternites; (16) antenna. T. bundjalong 17–20: (17) head; (18) metanotum & pelta; (19) tergites IX–X; (20) male sternite VIII. T. burroughsi 21–22: (21) head & pronotum; (22) metanotum & pelta. T. bursariicola (=ater) 23–26: (23) head & pronotum, Female; (24) head & pronotum, Male; (25) metanotum & pelta; (26) male sternite VIII.
FIGURES 37–43 in Structural diversity among the leaf-feeding thrips of Australia in the genus Teuchothrips (Thysanoptera, Phlaeothripinae) with 20 new species
FIGURES 37–43. Teuchothrips of Australia. T. gangarru 37–40: (37) head & pronotum; (38) antenna; (39) male sternite VIII; (40) metanotum & pelta. T. garrunggam 41–43: (41) head & pronotum; (42) antenna; (43) fore wing sub-basal setae.
Predicting time series of vegetation leaf area index across North America based on climate variables for land surface modeling using attention-enhanced LSTM
<p>We developed an attention-enhanced long and short memory (AELSTM) model for predicting vegetation LAI time series based on climatic data. The developed AELSTM model establishes the relationships between the time series of vegetation LAI and climatic variables. </p>
Supplementary material 7 from: Cumming RT, Bank S, Le Tirant S, Bradler S (2020) Notes on the leaf insects of the genus Phyllium of Sumatra and Java, Indonesia, including the description of two new species with purple coxae (Phasmatodea, Phylliidae). ZooKeys 913: 89-126. https://doi.org/10.3897/zookeys.913.49044
File S3. Deposition of paratype material for Phyllium (Phyllium) gardabagusi sp. nov. and Phyllium (Phyllium) nisus sp. nov.
Supplementary material 1 from: Cumming RT, Bank S, Le Tirant S, Bradler S (2020) Notes on the leaf insects of the genus Phyllium of Sumatra and Java, Indonesia, including the description of two new species with purple coxae (Phasmatodea, Phylliidae). ZooKeys 913: 89-126. https://doi.org/10.3897/zookeys.913.49044
Table S1. GenBank accession numbers for 55 sequences from Phyllium specimens, including sex, type designation, specimen collection code, and collection data
Ganesha on a Leaf
The Leaf Ganesha was 3D Scanned at **Addere Creations**. 3D Scan Process: **Photogrammetry** Number of Photos used: 53 Source: Objaverse 1.0 / Sketchfab
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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