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Supplementary material 2 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure S2. Maximum-likelihood tree of the complete set of taxa inferred with RAxML : Explanation note: Support values as in Figure S1.
Supplementary material 1 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure S1. Maximum-likelihood tree of the complete set of taxa inferred with IQ-TREE : Explanation note: This tree is identical to the one shown in Figs 2–12 except that it includes all outgroups and all support values are shown (in the sequence SBS / RBS / SH-like aLRT).
Data used for the paper Daniel Malko, Yanjun Guo, Pip Jones, George Britovsek, and Anthony Kucernak, "Heterogeneous iron containing carbon catalyst (Fe-N/C) for epoxidation with molecular oxygen|", Journal of Catalysis, 2019, DOI:10.1016/j.jcat.2019.01.008
<p>The data in this spreadsheet was used to produce the figures in the paper</p> <p>Daniel Malko, Yanjun Guo, Pip Jones, George Britovsek, and Anthony Kucernak</p> <p>Heterogeneous iron containing carbon catalyst (Fe-N/C) for epoxidation with molecular oxygen</p> <p>Journal of Catalysis</p> <p>DOI:10.1016/j.jcat.2019.01.008</p> <p>Please cite the above reference if you wish to use this data<br> DOI of this data file is: 10.5281/zenodo.2539183</p>
FIGURES 27–32 in Cephalomalthinus simplicicornis (Wittmer, 1993) rev. stat. et comb. n.: a resurrected soldier beetle (Coleoptera, Cantharidae) from Taiwan based on morphological and molecular data
FIGURES 27–32. Abdominal ventrite VII of female, ventral view: 27–28. Cephalomalthinus simplicicornis (Wittmer) rev. stat. et comb. n. Female genitalia, lateral view: 29–30. C. formosanus (Pic); 31–32. C. simplicicornis (Wittmer) rev. stat. et comb. Scale bar: 0.5 mm.
FIGURES 21–26 in Cephalomalthinus simplicicornis (Wittmer, 1993) rev. stat. et comb. n.: a resurrected soldier beetle (Coleoptera, Cantharidae) from Taiwan based on morphological and molecular data
FIGURES 21–26. Inner sac of aedeagus: 21–23. Cephalomalthinus formosanus (Pic); 24–26. C. simplicicornis (Wittmer) rev. stat. et comb. n. Ventral view: 21, 24; dorsal view: 22, 25; lateral view: 23, 26. Scale bar: 0.5 mm.
FIGURES 11–14 in Cephalomalthinus simplicicornis (Wittmer, 1993) rev. stat. et comb. n.: a resurrected soldier beetle (Coleoptera, Cantharidae) from Taiwan based on morphological and molecular data
FIGURES 11–14. Head of males, dorsal view: 11–12. Cephalomalthinus formosanus (Pic); 13–14. C. simplicicornis (Wittmer) rev. stat. et comb. n.
FIGURES 15–20 in Cephalomalthinus simplicicornis (Wittmer, 1993) rev. stat. et comb. n.: a resurrected soldier beetle (Coleoptera, Cantharidae) from Taiwan based on morphological and molecular data
FIGURES 15–20. Conjoint dorsal plate of parameres, dorsal view: 15–16. Cephalomalthinus formosanus (Pic); 17–20. C. simplicicornis (Wittmer) rev. stat. et comb. n. Dorsal processes of median lobe indicated by blue arrows. Variation in form of median lobe showed in Fig. 20. Non-type specimens: 15–18; holotype: 19. Scale bar: 1.0 mm.
FIGURES 2–10 in Cephalomalthinus simplicicornis (Wittmer, 1993) rev. stat. et comb. n.: a resurrected soldier beetle (Coleoptera, Cantharidae) from Taiwan based on morphological and molecular data
FIGURES 2–10. Habitus, dorsal view: 2–4. Cephalomalthinus formosanus (Pic); 5–10. C. simplicicornis (Wittmer) rev. stat. et comb. n. Males: 2–3, 5–7, 10; females: 4, 8–9. Non-type specimens: 2–9; holotype: 10. Scale bar: 5.0 mm.
FIGURE 1 in Cephalomalthinus simplicicornis (Wittmer, 1993) rev. stat. et comb. n.: a resurrected soldier beetle (Coleoptera, Cantharidae) from Taiwan based on morphological and molecular data
FIGURE 1. Neighbor joining (NJ) tree of soldier beetles inferred from mitochondrial COI gene. Bootstrapping values of NJ (left), ML (middle), and those of posterior probabilities from Bayesian inference (BI) (right) with more than 50% are shown at nodes.
FIGURE 9 in Congruence between morphology and molecular data supports the distinction between the snapping shrimps Alpheus macrocheles and A. amblyonyx (Caridea, Alpheidae)
FIGURE 9. Localities of origin of the specimens of Alpheus macrocheles (Hailstone, 1835b) (red) and A. amblyonyx Chace, 1972 (blue) used in the morphology analysis (solid circles), or for both morphology and genetics (solid squares). Type localities are indicated with a letter X. The black arrow indicates the location of the neotype.
FIGURE 5. Alpheus amblyonyx Chace, 1972 in Congruence between morphology and molecular data supports the distinction between the snapping shrimps Alpheus macrocheles and A. amblyonyx (Caridea, Alpheidae)
FIGURE 5. Alpheus amblyonyx Chace, 1972, ovigerous female specimen from Guadeloupe, MNHN 12112. (A) major cheliped, lateral view; (B) same, mesial view; (C) minor cheliped, lateral view; (D) same, mesial view; (E, F) detail of the spiniform setae in the ischium and propodus of the major and minor chelae, respectively; (G) dactylus of the major chelae, mesial in mesial view, detail on the plunger. Scale bars: A–E, 1 mm; F, G, 0.5 mm.
FIGURE 1 in Congruence between morphology and molecular data supports the distinction between the snapping shrimps Alpheus macrocheles and A. amblyonyx (Caridea, Alpheidae)
FIGURE 1. Alpheus macrocheles (Hailstone, 1835b), neotype male specimen from Roscoff, France, RMHN.Crus.D.29789. (A) Carapace and cephalic appendages, dorsal view (setae omitted); (B) same, lateral view; (C) ventromesial carina of the antennular peduncle; (D) left mandible, mesial view; (E) first maxilla, lateral view; (F) second maxilla, lateral view; (G) first maxilliped, lateral view; (H) second maxilliped, lateral view; (I) third maxilliped, lateral view; (J) telson and uropods, dorsal view (setae omitted). Scale bars: A, B, I, J, 1 mm; C–H, 0.5 mm.
FIGURE 4. Alpheus amblyonyx Chace, 1972 in Congruence between morphology and molecular data supports the distinction between the snapping shrimps Alpheus macrocheles and A. amblyonyx (Caridea, Alpheidae)
FIGURE 4. Alpheus amblyonyx Chace, 1972, male specimen from Quintana Roo, Mexico, CNCR 21271. (A) Carapace and cephalic appendages, dorsal view (setae omitted); (B) same, lateral view; (C) ventromesial carina of the antennular peduncle; (D) third maxilliped, lateral view; (E) telson and uropods, dorsal view (setae omitted); (F) uropod, detail of the distal margin of endopod, setae ommited. Scale bars: A, B, D, E, F, 1 mm; C, 0.5 mm.
FIGURE 6. Alpheus amblyonyx Chace, 1972 in Congruence between morphology and molecular data supports the distinction between the snapping shrimps Alpheus macrocheles and A. amblyonyx (Caridea, Alpheidae)
FIGURE 6. Alpheus amblyonyx Chace, 1972, ovigerous female specimen from Guadeloupe, MNHN 12112. (A) second pereiopod, lateral view; (B) third pereiopod, lateral view; (C) fourth pereiopod, lateral view; (D) fifth pereiopod, lateral view; (E–G) third–fifth pereiopods, detail of the propodus; (H, I) third and fourth pereiopods in lateral view, detail of the dactylus. Scale bars: A–D, 1 mm; E–I, 0.5 mm.
FIGURE 8 in Congruence between morphology and molecular data supports the distinction between the snapping shrimps Alpheus macrocheles and A. amblyonyx (Caridea, Alpheidae)
FIGURE 8. Bayesian Inference Tree of 16S gene among specimens of Alpheus macrocheles (Hailstone, 1835b) and Alpheus amblyonyx Chace, 1972 and other snapping shrimp of the genus Alpheus Fabricius, 1798 and Synalpheus Spence Bate, 1888. CNCR: Colección Nacional de Crustáceos, Mexico; MNHN: Muséum national d'Histoire naturelle, France; RMNH: Netherlands Centre for Biodiversity Naturalis; OUMNH: Oxford University Museum of Natural History; UF: Florida Museum of Natural History; ULLZ: University of Louisiana at Lafayette Zoological Collection. Numbers close to nodes represent posterior probabilities.
FIGURE 2 in Congruence between morphology and molecular data supports the distinction between the snapping shrimps Alpheus macrocheles and A. amblyonyx (Caridea, Alpheidae)
FIGURE 2. Alpheus macrocheles (Hailstone, 1835b), (A, B, E) neotype male specimen from Roscoff, France, RMHN.Crus. D.29789; (G, H, F) female specimen from Roscoff France, RMHN 34508; (C, D, J), male specimen from Azores, RMNH.Crus. D.51342: (A, C) major cheliped in lateral view; (B, D) same, in mesial view; (E, F) detail of the spiniform setae on the ischium and propodus of the major and minor chelae, respectively; (G) minor cheliped, lateral view; (H) same, mesial view; (I, J) dactylus of the major chelae in mesial view, detail of the plunger. Scale bars: A–H, 1 mm; I, J, 0.5 mm.
FIGURES 11–16 in A new species of Heliothrips (Thysanoptera, Panchaetothripinae), based on morphological and molecular data
FIGURES 11–16. Heliothrips species from China. Meso– and metanotum, 11–12: (11) longisensibilis sp. n.; (12) haemorrhoidalis; Antennae, 13–14: (13) longisensibilis sp.n.; (14) haemorrhoidalis; Abdominal tergites VIII–X of female, 15–16: (15) longisensibilis sp. n.; (16) haemorrhoidalis.
FIGURES 1–10 in A new species of Heliothrips (Thysanoptera, Panchaetothripinae), based on morphological and molecular data
FIGURES 1–10. Heliothrips longisensibilis sp. n. (1) Female; (2) Teneral Female; (3) Male; (4) Head and pronotum; (5) Abdominal tergites IV–VI; (6) Prospinasternum; (7) Abdominal tergite I; (8) Abdominal sternites III–IV of male; (9) Abdominal tergites VIII–X of male; (10) Fore wing.
FIGURE 17 in A new species of Heliothrips (Thysanoptera, Panchaetothripinae), based on morphological and molecular data
FIGURE 17. Neighbour-joining tree of two species of Heliothrips based on mitochondrial COI sequences (a) and combined nuclear ITS2+28S+EF-1α sequences (b), using Kimura 2-parameter distance. Bootstrap values are calculated in MEGA7.0 with 1000 replicates. Voucher number, species name, origin and GenBank Accession number are shown in the right column.
FIGURE 14. Consensus tree obtained from a 847 in The identity of some specimens previously (mis)identified as Rhinoleucophenga obesa (Loew) (Diptera: Drosophilidae) in Brazil, based on morphological and molecular data, with implications on distribution
FIGURE 14. Consensus tree obtained from a 847-bp alignment of cytochrome c oxidase subunit I (COI) gene sequences of Rhinoleucophenga specimens. Above the branches, support values by Neighbour-joining (10,000 bootstrap replications) and posterior probabilities values using Bayesian inference (1,000,000 generations), respectively.
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Allen Brain Atlas
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International Brain Laboratory public data
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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.