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Fig. 1 in Understanding the tangled taxonomy of the genus Pseudohercostomus Stackelberg, 1931 (Insecta: Diptera: Dolichopodidae) with description of new species from Singapore and DR Congo
Fig. 1. Pseudohercostomus singaporensis, new species, male habitus. Paratype (Kranji Marshes, KM04 (ZRC_BDP0243029, ZRC)). Photo credit: Rene Ong. Abbreviation: metep: metepimeron.
Fig. 5 in Understanding the tangled taxonomy of the genus Pseudohercostomus Stackelberg, 1931 (Insecta: Diptera: Dolichopodidae) with description of new species from Singapore and DR Congo
Fig. 5. Pseudohercostomus congoensis, new species, male. Holotype [Lake Edward, Rwindi r., Albert National Park (Virunga National Park), DR Congo]. A, habitus lateral; B, mesoscutum dorsal; C, head. (RMCA, photo credit: I. Van de Velde)
Fig. 2 in Taxonomy of the Ranatra biroi group sensu Lansbury, 1972 (Nepomorpha: Nepidae), with descriptions of two new species
Fig. 2. Ranatra luzonensis, new species, male holotype. A, habitus; B, head, prothorax, and fore legs, dorsal view; C, head and prothorax, lateral view; D, antenna; E, metasternum; F, operculum; G, left paramere, lateral view. B, C same scale; E, F same scale.
Fig. 1 in Taxonomy of the Ranatra biroi group sensu Lansbury, 1972 (Nepomorpha: Nepidae), with descriptions of two new species
Fig. 1. Parameres of Ranatra species. A, Ranatra digitata, from Sri Lanka (ZRC_ENT00013064); B, R. biroi, from Irian Jaya, Indonesia; C, R. rafflesi, holotype; D, R. rafflesi, from West Kalimantan, intermediate form (ZRC_ENT00013018); E, R. rafflesi, from West Kalimantan, slender form (ZRC_ENT00013054). C, D, E same scale.
Fig. 3 in Novitates neocaledonicae. VIII. Taxonomie et nomenclature du genre Phelline (Phellinaceae) avec la description de la nouvelle espèce Phelline barrierei
Fig. 3. – Distribution de Phelline barrierei Barriera & Schlüssel sur la Grande Terre, en gris les zones à roches ultramafiques.
Fig. 2 in Novitates neocaledonicae. VIII. Taxonomie et nomenclature du genre Phelline (Phellinaceae) avec la description de la nouvelle espèce Phelline barrierei
Fig. 2. – Phelline barrierei Barriera & Schlüssel. A. Habitus; B. Inflorescence femelle; C. Jeune infrutescence.
Fig. 1 in Novitates neocaledonicae. VIII. Taxonomie et nomenclature du genre Phelline (Phellinaceae) avec la description de la nouvelle espèce Phelline barrierei
Fig. 1 – Phelline barrierei Barriera & Schlüssel. A. Rameau femelle; B. Fleurs femelles; C. Fleurs mâles; D. Fruit immature; E. Inflorescence mâle; F. Jeune infrutescence.
Figure 2 in Taxonomy And Phylogenetics Of The Peromyscus Maniculatus Species Group
Figure 2. Maximum parsimony tree derived from sequence variation (ND3/ND4/ND4L) for the northeastern, central and western samples of Peromyscus maniculatus and reference sequences for P. sejugis, P. gambelii, P. keeni, P. polionotus, P. melanotis, and P. leucopus. Numbers associated with the branches are maximum parsimony bootstrap values and Bayesian posterior probabilities. Locality and GenBank references are given in the Materials and Methods.
Fig. 5 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Comoros
Fig. 5. Western Indian Ocean Hymenophyllum subg. Mecodium, illustrating morphological resemblance of taxa which are difficult to distinguish (see text). A. Hymenophyllum kuhnii C.Chr. from Comoros, firstly identified as H. polyanthos (Sw.) Sw. (F.Rakotondrainibe et al. 6864, P00312328). B. Hymenophyllum capense Schrad. from Madagascar, initially identified as H. fumarioides Bory ex Willd. (F.Rakotondrainibe et al. 6121, P00212664). C. Syntype of Hymenophyllum kuhnii C.Chr. from Tanzania (B200092782). D. Hymenophyllum inaequale (Poir.) Desv., representative specimen from La Réunion (L.Bauret 190, P).
Fig. 2 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Comoros
Fig. 2. Illustration of representative descriptors and states used in the Xper database (see Appendix 1). A. Hymenophyllum hirsutum (L.) Sw., typical bilabiate sori (S) without a developed base, fully hairy lamina with pedunculated brown trichomes (see inset). B. Didymoglossum robinsonii (Hook. ex Baker) Copel., false veins (FV) parallel but not connected to true veins (TV) and marginal dark trichomes clustered here by 6 (see inset). C. Crepidomanes inopinatum (Pic.Serm.) J.P.Roux, typical trichomanoid sori (S) with a developed tubular base, lips are here dilated as a collar. D. Didymoglossum rotundifolium (Bonap.) J.P.Roux, false veins (FV) parallel but not connected to true veins (TV) and continuous submarginal false vein (smFV), here the one-cell thick lamina appears well translucent. E. Crepidomanes bipunctatum (Poir.) Copel., false veins more or less continuous and parallel to margins (mFV) and not connected to true veins (TV). F. Hymenophyllum sibthorpioides (Bory ex Willd.) Mett. ex Kuhn, bilabiate sori (S) with toothed margins. Photographs by A.H. Saïd.
Fig. 4. Terrestrial Comorian Hymenophyllaceae. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Comoros
Fig. 4. Terrestrial Comorian Hymenophyllaceae. A. Abrodictyum pseudorigidum Bauret & Dubuisson, first identified as A. rigidum (Sw.) Ebihara & Dubuisson, (F.Rakotondrainibe et al. 6771, P00312031). B. Trichomanes boivinii Bosch, new for the archipelago according to the last inventories (as discussed in text) (F.Rakotondrainibe et al. 6675, P00311390). Scale bar for both species = 3 cm.
Fig. 3 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Comoros
Fig. 3. Representative Comorian Hymenophyllaceae as observed in situ in rainforests (here from Grande Comore or Mohéli). A. Endemic Didymoglossum kirkii (Hook.) Ebihara & Dubuisson (G.Rouhan et al. 925, P00684886). B. Hymenophyllum sibthorpioides (Bory ex Willd.) Mett. ex Kuhn (G.Rouhan et al. 888, P02439806). C. Didymoglossum hildebrandtii (Kuhn) Ebihara & Dubuisson (M.Pignal et al. 3456, P02439793). D. Hymenophyllum kuhnii C.Chr. (G.Rouhan 897, P02439807). E. Crepidomanes bipunctatum (Poir.) Copel. (G.Rouhan et al. 882, P02439805). F. Hymenophyllum hirsutum (L.) Sw. (M.Pignal et al. 3487, P02439796). Photographs by G. Rouhan. Scale bars = 1 cm.
Fig. 1 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Comoros
Fig. 1. Location of the Comoros archipelago in the western Indian Ocean; close-up on the four islands in grey inset; islands in white form the Union of Comoros, Mayotte in grey is a French overseas department.
Fig. 1. A in "A character does not make a genus, but the genus makes the character ": three-taxon statement analysis and intuitive taxonomy
Fig. 1. A. Strict consensus of 61 most parsimonious phylogenetic trees; tree length = 90 steps; CI = 0.6000; RI = 0.8302, recovered from a standard cladistic analysis (MP) (Fitch Parsimony) of the complete conventionalmorphologicalmatrixof Atraphaxis s. l. (TableS1).All 27 unordered (non-additive) characters are parsimony informative. B. Strict consensus of two nested most parsimonious hierarchies of patterns; length = 8328 steps; CI = 0.8521; RI = 0.8264), recovered from a MP analysis of the three-taxon statement representation of the complete conventional 27 characters' morphological matrix of Atraphaxis s. l. (Table S1). The number of 3TSs (characters) is equal to 7096, all are parsimony-informative. C. Strict consensus of six most parsimonious phylogenetic trees; tree length = 56 steps; CI = 0.6071; RI = 0.8370, recovered from a MP analysis of the reduced conventional 18 characters' morphological matrix of Atraphaxis s. l. (Table S1) with the characters one, two, four, eight, 12, 16, 18, 19, and 26 excluded. D. Strict consensus of two nested, most parsimonious hierarchies of patterns; length = 5844 steps; CI = 0.8665; RI = 0.8460), recovered from a MP analysis of the three-taxon statement representation of the reduced conventional 18 characters' morphological matrix of Atraphaxis s. l. (Table S1) with characters 1, 2, 4, 8, 12, 16, 18, 19 and 26 excluded. The number of 3TSs (characters) is equal to 5064, all are parsimony-informative. All MP analyses as in PAUP* 4.0a150 (Swofford 2002) were conducted using either conventional matrices or TAXODIUM's output 3TS NEXUS files with a heuristic search of 1000 random addition replicates (saving no more than 100 trees per replicate), and the TBR branch swapping/MulTrees option into effect. Branches with a minimum length of zero were collapsed. The three-taxon statement analysis (3TA) of the unordered morphological matrix was established after it three-taxon (3TS) Williams-Siebert (WS) representation (Williams & Siebert 2000) using TAXODIUM v. 1.2 (Mavrodiev & Madorsky 2012). The 3TS permutations were performed with the following command: taxodium input_file_name. csv –ium –ob –og –nex The value of the operational outgroup was fixed as a value of Bactria lazkovii. All 3TSs were weighted uniformly and treated as ''ordered'' (Wagner Parsimony). The bootstrap resampling of both conventional and 3TS matrices have been performed as described in Mavrodiev & Madorsky (2012). The diagnostic traits are optimized using Mesquite (Maddison & Maddison 2011).
FIGURE 1 in Folk taxonomy of the gray mullets (Mugilidae: Mugiliformes) in a marine extractivist reserve of northern Brazil
FIGURE 1 | Map of Ajuruteua Plateau, on the northern coast of Brazil, showing the two villages at which the ethnotaxonomic data on the fish of the family Mugilidae were collected in the present study.
FIGURE 4 in Folk taxonomy of the gray mullets (Mugilidae: Mugiliformes) in a marine extractivist reserve of northern Brazil
FIGURE 4 | Results of the Redundancy Analysis (RDA) of the definition of the ethnospecies by the artisanal fishers from the Caeté-Taperaçu Marine Extractive Reserve in Bragança, northern Brazil, with the characteristics that best identify each taxon. A. CA: 'caica', PA: 'pratiqueira', PR: 'pratiqueira/ ribação', SR: 'sajuba/ribação', RI: 'ribação', UR: 'urubarana', PQ: 'pratiqueirão', FI: 'filhotes'; B: narrow body, B1: juvenile of large mullet, D: does not grow a lot, G: narrow headed, I: small headed, M: small eyed, P: small scales, U: does not jump, Z: smells. B. TA: 'tainha', TM: 'tainha macho', TBR: 'tainha branca', TB: 'tainha boi', TC: 'tainha chata', TGP: 'tainha grande/puá', TG: 'tainha grande', TCU: 'tainha curimã', CT: 'caica tamatarana', SA: 'sajuba', A: rounded body, C: grows a lot, E: back dark/bluish, F: flattened head, H: rounded head, J: large headed, L: large eyed, N: red eyed, O: large scales, Q: rounded scales, R: shiny scales, S: scales close together, V: smart, X: stupid. C. PB: 'pratiqueira/barrasco', BA: 'barrasco', BR: 'barrasco/ribação', SBR: 'sajuba/barrasco/ribação', IR: 'irichona', A1: sexual dimorphism, C1: 'baby mullet'.
FIGURE 3 in Folk taxonomy of the gray mullets (Mugilidae: Mugiliformes) in a marine extractivist reserve of northern Brazil
FIGURE 3 | Folk taxonomy designated by the artisanal fishers of the Caeté-Taperaçu Marine Extractive Reserve for the gray mullet (Mugilidae) and the corresponding scientific classification. The numbers within parentheses indicate the number of fishers reporting the ethnospecies. * = the number of fishers who stated that they did not know the ethnospecies or that it did not occur in the region.
FIGURE 2 in Folk taxonomy of the gray mullets (Mugilidae: Mugiliformes) in a marine extractivist reserve of northern Brazil
FIGURE 2 | Morphological features of a gray mullet (Mugilidae), showing the terminology used by the fishers of the Caeté-Taperaçu Marine Extractive Reserve in Bragança, Pará, Brazil.
Supplementary Fig. 1 in Two new species of Eleutherodactylus (Anura: Eleutherodactylidae) from Southern Mexico, with comments on the taxonomy of related species and their advertisement calls
Supplementary Fig. 1. Bayesian phylogenetic inference of members of the Eleutherodactylus subgenus Syrrhophus, based on the mitochondrial loci 16S rRNA. All nodes with support of less than 0.5 are collapsed.
Fig. 7 in Two new species of Eleutherodactylus (Anura: Eleutherodactylidae) from Southern Mexico, with comments on the taxonomy of related species and their advertisement calls
Fig. 7. (A) Map showing the type localities and distribution of Eleutherodactylus species related to E. nitidus in southern Mexico. The stars represent type localities and circles represent additional localities, with each color coded for the species: E. sentinelus sp. nov. (purple), E. maculabialis sp. nov. (green), E. dilatus (pink), E. maurus (yellow), and E. syristes (blue). (B) Map showing the type localities and distribution of Eleutherodactylus species related to E. pipilans in southern Mexico. The red star represents the type locality of E. pipilans and red circles represent additional localities. The black star represents the type locality of E. nebulosus and black circles represent additional localities.
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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
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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.