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Figs 57–66. Antenna. 57. Ecacanthothrips tibialis. 58. Holothrips flavus. 59. Hoplandrothrips bidens. 60. Hoplandrothrips coloratus. 61. Hoplandrothrips flavipes. 62. Hoplandrothrips nobilis. 63. Hoplandrothrips obesametae. 64. Hoplandrothrips ochraceus. 65. Hoplothrips orientalis. 66 in Key to the fungus-feeder Phlaeothripinae species from China (Thysanoptera: Phlaeothripidae)
Figs 57–66. Antenna. 57. Ecacanthothrips tibialis. 58. Holothrips flavus. 59. Hoplandrothrips bidens. 60. Hoplandrothrips coloratus. 61. Hoplandrothrips flavipes. 62. Hoplandrothrips nobilis. 63. Hoplandrothrips obesametae. 64. Hoplandrothrips ochraceus. 65. Hoplothrips orientalis. 66. Hyidiothrips brunneus.
Table 2 in Phytotoxic activity of extracts obtained from cagaita (Eugenia dysenterica DC. - Myrtaceae) on the growth of black-jack (Bidens pilosa L.)
<p>Table 2. Effect of different leaf and stem bark extracts of <i>Eugenia dysenterica</i> DC. on the germination speed index (GSI) of <i>Bidens pilosa</i> L. seeds.</p><table><tbody><tr><th><b>Concentration (<b>mgL-</b> 1<b>)</b></b></th><th><b>LAE</b></th><th><b>LEE</b></th><th><b>LHE 70:30</b></th><th><b>LHE 50:50</b></th><th><b>SAE</b></th><th><b>SEE</b></th><th><b>SHE 70:30</b></th><th><b>SHE 50:50</b></th></tr></tbody><tbody><tr><th>0</th><td>18.20 A</td><td>18.20 A</td><td>18.20 A</td><td>18.20 A</td><td>18.20 A</td><td>18.20 A</td><td>18.20 A</td><td>18.20 A</td></tr><tr><th>250</th><td>15.10 B</td><td>13.60 B</td><td>9.95 B</td><td>7.30 B</td><td>10.60 B</td><td>13.30 B</td><td>12.90 B</td><td>14.20 B</td></tr><tr><th>500</th><td>19.61 A</td><td>12.20 B</td><td>8.18 B</td><td>9.60 B</td><td>9.65 B</td><td>12.20 B</td><td>8.41 C</td><td>9.79 C</td></tr><tr><th>1000</th><td>11.75 C</td><td>7.70 C</td><td>7.61 B</td><td>9.94 B</td><td>9.40 B</td><td>8.04 C</td><td>8.10 C</td><td>9.68 C</td></tr></tbody></table><p>Means followed by the same letter in the column do not differ from each other by the Tukey test at 5% probability. Leaf Aqueous Extract (LAE), Leaf Ethanolic Extract (LEE), Leaf Hydroalcoholic Extract 70:30 (LHE 70:30), Leaf Hydroalcoholic Extract 50:50 (LHE 50:50), Stem aqueous extract (SAE), Stem ethanolic extract (SEE), Stem hydroalcoholic extract 70:30 (SHE 70:30), and Stem hydroalcoholic extract 50:50 (SHE 50:50).</p>
Table 1 in Phytotoxic activity of extracts obtained from cagaita (Eugenia dysenterica DC. - Myrtaceae) on the growth of black-jack (Bidens pilosa L.)
<p><b>Table 1</b>. Effect of different leaf and stem bark extracts of <i>Eugenia dysenterica</i> DC. on the germination percentage (G%) of <i>Bidens pilosa</i> L. seeds.</p><table><tbody><tr><th><b>Concentration (<b>mgL-</b> 1<b>)</b></b></th><th><b>LAE</b></th><th><b>LEE</b></th><th><b>LHE 70:30</b></th><th><b>LHE 50:50</b></th><th><b>SAE</b></th><th><b>SEE</b></th><th><b>SHE 70:30</b></th><th><b>SHE 50:50</b></th></tr></tbody><tbody><tr><th>0</th><td>64.00 A</td><td>64.00 A</td><td>64.00 A</td><td>64.00 A</td><td>64.00 A</td><td>64.00 A</td><td>64.00 A</td><td>64.00 A</td></tr><tr><th>250</th><td>59.84 A</td><td>59.14 A</td><td>60.33 A</td><td>59.35 A</td><td>59.18 A</td><td>58.81 A</td><td>58.16 A</td><td>59.11 A</td></tr><tr><th>500</th><td>57.48 A</td><td>59.76 A</td><td>41.56 B</td><td>42.00 B</td><td>57.00 A</td><td>57.25 A</td><td>48.16 B</td><td>42.48 B</td></tr><tr><th>1000</th><td>58.75 A</td><td>57.70 A</td><td>40.18 B</td><td>41.14 B</td><td>59.40 A</td><td>58.14 A</td><td>42.12 B</td><td>41.18 B</td></tr></tbody></table><p>Means followed by the same letter in the column do not differ from each other by the Tukey test at 5% probability. Leaf Aqueous Extract (LAE), Leaf Ethanolic Extract (LEE), Leaf Hydroalcoholic Extract 70:30 (LHE 70:30), Leaf Hydroalcoholic Extract 50:50 (LHE 50:50), Stem aqueous extract (SAE), Stem ethanolic extract (SEE), Stem hydroalcoholic extract 70:30 (SHE 70:30), and Stem hydroalcoholic extract 50:50 (SHE 50:50).</p>
Interactive effects of rhizospheric soil microbes and litter on the growth of the invasive hyperaccumulator Bidens pilosa in cadmium-contaminated soil
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FIGURE 42. a Neogomphus bidens, abdomen S6–10 in The Odonata (Insecta) of Patagonia: A synopsis of their current status with illustrated keys for their identification
FIGURE 42. a Neogomphus bidens, abdomen S6–10, dorsal view; b Neogomphus edenticulatus, abdomen S6–10, dorsal view.
FIGURES 5–8. Limonia bidens. 5 in Limonia crane flies (Diptera: Limoniidae) of Korea
FIGURES 5–8. Limonia bidens. 5: male, general view; 6: wing; 7: male genitalia, dorsal view; 8: male genitalia, ventral view.
FIGURES 1–16. 1–4. Atherigona bidens Hennig, male terminalia. 1. Hypopygial prominence, dorsal view. 2. Male hypopygial prominence, lateral view. 3. Male trifoliate process, posterior view. 4. Male trifoliate process, lateral view. 5– 8. Atherigona oryzae Malloch, male terminal. 5. Hypopygial prominence, dorsal view. 6. Hypopygial prominence, lateral view. 7. Trifoliate process, posterior view. 8. Trifoliate process, lateral view. 9–12 in The Muscidae (Diptera) of New Caledonia 2503
FIGURES 1–16. 1–4. Atherigona bidens Hennig, male terminalia. 1. Hypopygial prominence, dorsal view. 2. Male hypopygial prominence, lateral view. 3. Male trifoliate process, posterior view. 4. Male trifoliate process, lateral view. 5– 8. Atherigona oryzae Malloch, male terminal. 5. Hypopygial prominence, dorsal view. 6. Hypopygial prominence, lateral view. 7. Trifoliate process, posterior view. 8. Trifoliate process, lateral view. 9–12. Atherigona simplex (Thomson), male terminalia. 9. Hypopygial prominence, dorsal view. 10. Hypopygial prominence, lateral view. 11. Trifoliate process, posterior view. 12. Trifoliate process, lateral view. 13–16. Atherigona tibiseta Malloch, male terminalia. 13. Hypopygial prominence, dorsal view. 14. Hypopygial prominence, lateral view. 15. Trifoliate process, posterior view. 16. Trifoliate process, lateral view. Scale bar: 0.1mm
Dataset for: Differential responses to fertilization and competition among invasive, non-invasive alien and native Bidens species
<p class="manuscript">Comparative studies of invasive, non-invasive alien, and native congenic plant species can identify plant traits that drive invasiveness. In particular, functional traits associated with rapid growth rate and high fecundity likely facilitate invasive success. As such traits often exhibit high phenotypic plasticity, characterizing plastic responses to anthropogenic environmental changes such as eutrophication and disturbance is important for predicting the invasive success of alien plant species in the future. Here, we compared trait expression and phenotypic plasticity at the species level among invasive, non-invasive alien, and native <i>Bidens</i> species. Plants were grown under nutrient addition and competition treatments, and their functional, morphological, and seed traits were examined. Invasive <i>B. frondosa</i> exhibited higher phenotypic plasticity in most measured traits than did the alien non-invasive <i>B. pilosa</i> or native <i>B. bipinnata</i>. However, differential plastic responses to environmental treatments rarely altered the rank of trait values among the three <i>Bidens</i> species, except for the number of inflorescences. The achene size of <i>B. frondosa</i> was larger, but its pappus length was shorter than that of <i>B. pilosa</i>. Two species demonstrated opposite plastic responses of pappus length to fertilization. These results suggest that the plasticity of functional traits does not significantly contribute to the invasive success of <i>B. frondosa</i>. The dispersal efficiency of <i>B. frondosa</i> is expected to be lower than that of <i>B. pilosa</i>, suggesting that long-distance dispersal is likely not a critical factor in determining invasive success.</p>
A genome for Bidens hawaiensis: a member of a hexaploid Hawaiian plant adaptive radiation
Abstract <p></p><p>The plant genus <em>Bidens</em> (Asteraceae or Compositae; Coreopsidae) is a species-rich and circumglobally distributed taxon. The 19 hexaploid species endemic to the Hawaiian Islands are considered an iconic example of adaptive radiation, of which many are imperiled and of high conservation concern. Until now, no genomic resources were available for this genus, which may serve as a model system for understanding the evolutionary genomics of explosive plant diversification. Here, we present a high-quality reference genome for the Hawai'i Island endemic species <em>B. hawaiensis</em> A. Gray reconstructed from long-read, high-fidelity sequences generated on a Pacific Biosciences Sequel II System. The haplotype-aware, draft genome assembly consisted of ~6.67 Giga bases (Gb), close to the holoploid genome size estimate of 7.56 Gb (± 0.44 SD) determined by flow cytometry. After removal of alternate haplotigs and contaminant filtering, the consensus haploid reference genome was comprised of 15,904 contigs containing ~3.48 Gb, with a contig N50 value of 422,594. The high interspersed repeat content of the genome, approximately 74%, along with hexaploid status, contributed to assembly fragmentation. Both the haplotype-aware and consensus haploid assemblies recovered >96% of Benchmarking Universal Single-copy Orthologs. Yet, the removal of alternate haplotigs did not substantially reduce the proportion of duplicated benchmarking genes (~79% versus ~68%). This reference genome will support future work on the speciation process during adaptive radiation, including resolving evolutionary relationships, determining the genomic basis of trait evolution, and supporting ongoing conservation efforts.</p><p></p>
On following pages: 74. Greater Long-tongued Blossom Bat (Macroglossus sobrinus); 75. Southern Blossom Bat (Syconycteris australis); 76. Halmaheran Blossom Bat (Syconycteris carolinae); 77. Moss-forest Blossom Bat (Syconycteris hobbit); 78. Manado Fruit Bat (Boneia bidens); 79. Sulawesi Harpy Fruit Bat (Harpyionycteris celebensis); 80. Philippine Harpy Fruit Bat (Harpyionycteris whitehead); 81. Bulmer's Fruit Bat (Aproteles bulmerae); 82. Lesser Naked-backed Fruit Bat (Dobsonia minor); 83. Moluccan Naked-backed Fruit Bat (Dobsonia moluccensis); 84. Western Naked-backed Fruit Bat (Dobsonia peronii); 85. Andersen's Naked-backed Fruit Bat (Dobsonia anderseni): 86. Panniet Naked-backed Fruit Bat (Dobsonia pannietensis); 87. Philippine Naked-backed Fruit Bat (Dobsonia chapman); 88. Biak Naked-backed Fruit Bat (Dobsonia emersa); 89. Sulawesi Naked-backed Fruit Bat (Dobsonia exoleta): 90. Greenish Naked-backed Fruit Bat (Dobsonia viridis); 91. Beaufort's Naked-backed Fruit Bat (Dobsonia beaufort); 92. Halmahera Naked-backed Fruit Bat (Dobsonia crenulata); 93. Solomons Naked-backed Fruit Bat (Dobsonia inermis); 94. New Britain Naked-backed Fruit Bat (Dobsonia praedatrix). in Pteropodidae
On following pages: 74. Greater Long-tongued Blossom Bat (Macroglossus sobrinus); 75. Southern Blossom Bat (Syconycteris australis); 76. Halmaheran Blossom Bat (Syconycteris carolinae); 77. Moss-forest Blossom Bat (Syconycteris hobbit); 78. Manado Fruit Bat (Boneia bidens); 79. Sulawesi Harpy Fruit Bat (Harpyionycteris celebensis); 80. Philippine Harpy Fruit Bat (Harpyionycteris whitehead); 81. Bulmer's Fruit Bat (Aproteles bulmerae); 82. Lesser Naked-backed Fruit Bat (Dobsonia minor); 83. Moluccan Naked-backed Fruit Bat (Dobsonia moluccensis); 84. Western Naked-backed Fruit Bat (Dobsonia peronii); 85. Andersen's Naked-backed Fruit Bat (Dobsonia anderseni): 86. Panniet Naked-backed Fruit Bat (Dobsonia pannietensis); 87. Philippine Naked-backed Fruit Bat (Dobsonia chapman); 88. Biak Naked-backed Fruit Bat (Dobsonia emersa); 89. Sulawesi Naked-backed Fruit Bat (Dobsonia exoleta): 90. Greenish Naked-backed Fruit Bat (Dobsonia viridis); 91. Beaufort's Naked-backed Fruit Bat (Dobsonia beaufort); 92. Halmahera Naked-backed Fruit Bat (Dobsonia crenulata); 93. Solomons Naked-backed Fruit Bat (Dobsonia inermis); 94. New Britain Naked-backed Fruit Bat (Dobsonia praedatrix).
On following pages: 146. Hairy Big-eyed Bat (Chiroderma villosum); 147. Brazilian Big-eyed Bat (Chiroderma doriae); 148. Vizotto's Big-eyed Bat (Chiroderma vizottoi); 149. Bidentate Yellow-eared Bat (Vampyriscus bidens); 150. Brock's Yellow-eared Bat (Vampyriscus brocki); 151. Striped Yellow-eared Bat (Vampyriscus nymphaea); 152. Baker's Tent-making Bat (Uroderma bakeri); 153. Common Tent-making Bat (Uroderma bilobatum); 154. Pacific Tent-making Bat (Uroderma convexum); 155. Davis's Tent-making Bat (Uroderma davisi); 156. Brown Tent-making Bat (Uroderma magnirostrum); 157. Kalko's Yellow-eared Bat (Vampyressa elisabethae); 158. Melissa's Yellow-eared Bat (Vampyressa melissa); 159. Quechuan Yellow-eared Bat (Vampyressa sinchi); 160. NorthernLittle Yellow-eared Bat (Vampyressa thyone); 161. Southern Little Yellow-eared Bat (Vampyressa pusilla); 162. MacConnell's Bat (Mesophylla macconnell)); 163. Caracciolo's Stripe-faced Bat (Vampyrodes caracciol)); 164. Great Stripe-faced Bat (Vampyrodes major). in Phyllostomidae
On following pages: 146. Hairy Big-eyed Bat (Chiroderma villosum); 147. Brazilian Big-eyed Bat (Chiroderma doriae); 148. Vizotto's Big-eyed Bat (Chiroderma vizottoi); 149. Bidentate Yellow-eared Bat (Vampyriscus bidens); 150. Brock's Yellow-eared Bat (Vampyriscus brocki); 151. Striped Yellow-eared Bat (Vampyriscus nymphaea); 152. Baker's Tent-making Bat (Uroderma bakeri); 153. Common Tent-making Bat (Uroderma bilobatum); 154. Pacific Tent-making Bat (Uroderma convexum); 155. Davis's Tent-making Bat (Uroderma davisi); 156. Brown Tent-making Bat (Uroderma magnirostrum); 157. Kalko's Yellow-eared Bat (Vampyressa elisabethae); 158. Melissa's Yellow-eared Bat (Vampyressa melissa); 159. Quechuan Yellow-eared Bat (Vampyressa sinchi); 160. NorthernLittle Yellow-eared Bat (Vampyressa thyone); 161. Southern Little Yellow-eared Bat (Vampyressa pusilla); 162. MacConnell's Bat (Mesophylla macconnell)); 163. Caracciolo's Stripe-faced Bat (Vampyrodes caracciol)); 164. Great Stripe-faced Bat (Vampyrodes major).
On following pages: 26. Striped Hairy-nosed Bat (Gardnerycteris crenulatum); 27. Keenan's Hairy-nosed Bat (Gardnerycteris keenani); 28. Koepcke's Hairy-nosed Bat (Gardnerycteris koepckeae); 29. Kalko's Round-eared Bat (Lophostoma kalkoae); 30. Pygmy Round-eared Bat (Lophostoma brasiliense); 31. Carriker's Round-eared Bat (Lophostoma carrikeri); 32. Schulz's Round-eared Bat (Lophostoma schulzi); 33. Western Round-eared Bat (Lophostoma occidentale); 34. Davis's Round-eared Bat (Lophostoma evotis); 35. White-throated Round-eared Bat (Lophostoma silvicola); 36. Greater Round-eared Bat (Tonatia bidens); 37. Stripe-headed Round-eared Bat (Tonatia saurophila); 38. Pale-faced Bat (Phylloderma stenops); 39. Pale Spearnosed Bat (Phyllostomus discolon; 40. Lesser Spearnosed Bat (Phyllostomus elongatus); 41. Greater Spearnosed Bat (Phyllostomus hastatus); 42. Guianan Spearnosed Bat (Phyllostomuslatifolius); 43. Woolly False Vampire Bat (Chrotopterus auritus); 44. Southern Golden Bat (Mimon bennett); 45. Cozumelan Golden Bat (Mimon cozumelae); 46. Spectral Bat (Vampyrum spectrum). in Phyllostomidae
On following pages: 26. Striped Hairy-nosed Bat (Gardnerycteris crenulatum); 27. Keenan's Hairy-nosed Bat (Gardnerycteris keenani); 28. Koepcke's Hairy-nosed Bat (Gardnerycteris koepckeae); 29. Kalko's Round-eared Bat (Lophostoma kalkoae); 30. Pygmy Round-eared Bat (Lophostoma brasiliense); 31. Carriker's Round-eared Bat (Lophostoma carrikeri); 32. Schulz's Round-eared Bat (Lophostoma schulzi); 33. Western Round-eared Bat (Lophostoma occidentale); 34. Davis's Round-eared Bat (Lophostoma evotis); 35. White-throated Round-eared Bat (Lophostoma silvicola); 36. Greater Round-eared Bat (Tonatia bidens); 37. Stripe-headed Round-eared Bat (Tonatia saurophila); 38. Pale-faced Bat (Phylloderma stenops); 39. Pale Spearnosed Bat (Phyllostomus discolon; 40. Lesser Spearnosed Bat (Phyllostomus elongatus); 41. Greater Spearnosed Bat (Phyllostomus hastatus); 42. Guianan Spearnosed Bat (Phyllostomuslatifolius); 43. Woolly False Vampire Bat (Chrotopterus auritus); 44. Southern Golden Bat (Mimon bennett); 45. Cozumelan Golden Bat (Mimon cozumelae); 46. Spectral Bat (Vampyrum spectrum).
On following pages: 18. Sowery's Beaked Whale (Mesoplodon bidens); 19. Blainville's Beaked Whale (Mesoplodon densirostris); 20. Andrews's Beaked Whale (Mesoplodon bowdoini); 21. Spade-toothed Whale (Mesoplodon traversil); 22. Gervais's Beaked Whale (Mesoplodon europaeus). in Ziphiidae
On following pages: 18. Sowery's Beaked Whale (Mesoplodon bidens); 19. Blainville's Beaked Whale (Mesoplodon densirostris); 20. Andrews's Beaked Whale (Mesoplodon bowdoini); 21. Spade-toothed Whale (Mesoplodon traversil); 22. Gervais's Beaked Whale (Mesoplodon europaeus).
FIGURE 1 in Description of the pupa of Culex (Culex) bidens Dyar (Diptera: Culicidae)
FIGURE 1. Culex (Culex) bidens. Pupa: a) Cephalothorax; b) abdomen. Male genitalia: c) Gonocoxite and gonostylus (lateral view); d) lateral plate, lateral surface; e) dorsal aspect of phallosome and proctiger. CT, cephalothorax; GL, genital lobe; Pa, paddle; I–VIII = abdominal segments I–VIII; 1–11,14 = setal numbers for specified areas. Note: Abdominal segment IX is not labelled but seta 1 of that segment is shown. Scales in millimeters.
Figure 3 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga
Figure 3: Temporal distribution of insect remains preyed upon by Tonatia bidens in the Brazilian Caatinga. (A) Richness, number of insect remains, and monthly rainfall recorded in each sampled month. (B) Richness and number of insect remains in the dry (September and October 2016, March and August 2017) and rainy (May and November 2022) seasons, considering all data gathered. Rainfall data from https://www.apac.pe.gov. br.
Figure 1 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga
Figure 1: Abundance of remains of different lepidopteran taxa sampled under feeding perches of the bat Tonatia bidens, in the Brazilian Caatinga. Data collected in September and October 2016, March and August 2017, and May and November 2022. Undet. = undetermined. Lepidopteran silhouettes were used under CC0 1.0 license (www.phylopic.org).
Figure 2 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga
Figure 2: Abundance of remains of different coleopteran taxa sampled under feeding perches of the bat Tonatia bidens, in the Brazilian Caatinga. Data collected in September and October 2016, March and August 2017, and May and November 2022. Coleopteran silhouettes were used under CC0 1.0 license (www.phylopic.org).
Data from: An unusual new species of Bidens (Asteraceae, Coreopsideae) with its phylogenetic position and taxonomic notes
An unusual new species of Bidens (Asteraceae) from Brazil is described and its placement within the genus is elucidated by phylogenetic analysis of ITS sequences. The new species, described as Bidens campanulata , is distinct in the genus based on its broadly campanulate corolla limb with long lobes, an extremely reduced involucre (shorter than the flower length), and the absence of awns on the pappus. This study presents a taxonomic treatment of the species of Bidens with discoid capitula endemic to the Brazilian Cerrado, including a key to the species, typification, and information on conservation status.
FIGURE 3. Pseudopalicus bidens new species. A–B in A new species of palicid crab (Crustacea, Decapoda: Brachyura: Palicidae) from the Andaman Sea, west coast of Thailand
FIGURE 3. Pseudopalicus bidens new species. A–B, Holotype male (8.1×10.4 mm) (PMBC 26820); C–F, Paratype male (7.8×10.0 mm) (PMBC 26821). A, ventral view; B, epistome, frontal view; C, male abdomen; D, left G1, dorsal view; E, left G1, apex, ventral view; F, left G1, apex, lateral view (inner side).
Dataset for: Differential responses to fertilization and competition among invasive, non-invasive alien and native Bidens species
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