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Figure 11 in A new classification of Callianassidae and related families (Crustacea: Decapoda: Axiidea) derived from a molecular phylogeny with morphological support
Figure 11. Diagnostic characters for genera of Callianassidae. Pleomere 6, telson, uropod: a, Arenallianassa; b, c, Caviallianassa (uropod in detail); d, e, Cheramoides (with pleomere 6 lateral); f, Gilvossius; g, Lipkecallianassa; h, Necallianassa; i, Neotrypaea californiensis; j, N. petalura; k, Notiax; l, Poti; m, Paratrypaea; n, Praedatrypaea; o, Pugnatrypaea; p, Tastrypaea. Original illustrations: a, Arenallianassa arenosa, NMV J31887; b, c, Caviallianassa FP-11, UF 29204; d, e, Cheramoides marginata, MNHN-IU-2016-2462; i, Neotrypaea californiensis, NMV J20600; i, N. petalura, NMV J59981; k, Notiax brachyophthalma, NMV J58880; m, Paratrypaea maldivensis, UF 28781.
Figure 20 in A new classification of Callianassidae and related families (Crustacea: Decapoda: Axiidea) derived from a molecular phylogeny with morphological support
Figure 20. Diagnostic characters for Paracalliacidae, Paracalliax bollorei: a, posterior carapace, pleomeres 1, 2; b, telson, uropod; c, maxilliped 3; d, e, female pleopods 1, 2.
Figure 15 in A new classification of Callianassidae and related families (Crustacea: Decapoda: Axiidea) derived from a molecular phylogeny with morphological support
Figure 15. Diagnostic characters for genera of Callichiridae. Male pleopod 1: a, Mocallichirus mocambiquensis; b, Balsscallichirus balssi; c, B. pixii; d, Corallianassa martensi; e, C. xutha; f, Glypturus armatus; g, Lepidophthalmus eiseni; h, L. madagassus; i, Neocallichirus raymanningi; j, N. vigilax. Male pleopod 2: k, Glypturus armatus; l, Corallianassa coutierei; m, Grynaminna tamakii; n, Michaelcallianassa indica. Female pleopod 2: o, Balsscallichirus balssi; p, Laticallichirus grandis. Original illustrations: a, Mocallichirus mocambiquensis, UF 13986; j, Neocallichirus vigilax MNHN-IU-2015-7072.
Figure 19 in A new classification of Callianassidae and related families (Crustacea: Decapoda: Axiidea) derived from a molecular phylogeny with morphological support
Figure 19. Diagnostic characters for genera of Eucalliacidae. Maxilliped 3: a, Calliaxina punica; b, C. SA-01; c, Andamancalliax; d, Eucalliaxiopsis; e, Pseudocalliax; f, Calliax. Male pleopod 1: g, h, Calliaxina bulimba; i, C. kensleyi; j, C. SA-01; k, C. punica; l, C. sakaii; m, Eucalliaxiopsis panglaoensis; n, E. mcilhennyi; o, p, E. inaequimana; q, Calliax; r, Pseudocalliax; s, Paraglypturus. Male pleopod 2: t, Calliaxina; u, v, Paraglypturus; w,Eucalliax; x,Eucalliaxiopsis. Female pleopod 2, y,Paraglypturus: z, Calliax; z', Calliaxina. Female pleopod 3: z'',Paraglypturus. Original illustrations: b, i, Calliaxina SA-01, UF 36699; g, C. bulimba, MNHN-IU-2013-7097; h, C. bulimba, NMV J71686; w, Eucalliax quadracuta, NHMW 25916; o, Eucalliaxiopsis inaequimana, MNHN-IU-2013-10008; p, E. inaequimana, UF 16512; e, r, Pseudocalliax tooradin NMV J303; u, v, Paraglypturus calderus, MNHN Th1416.
Figure 9 in A new classification of Callianassidae and related families (Crustacea: Decapoda: Axiidea) derived from a molecular phylogeny with morphological support
Figure 9. Diagnostic characters for genera of Callianassidae. Male major cheliped: a, Jocullianassa; b, Notiax; c, Necallianassa; d, Neotrypaea; e, f, Paratrypaea; g, Rayllianassa; h, Rudisullianassa; i, Scallasis; j, Spinicallianassa; k, Tastrypaea. Minor cheliped: l, Jocullianassa; m, Rudisullianassa.
Figure 5 in A TIME-CALIBRATED PHYLOGENY OF VERBESINA (HELIANTHEAE - ASTERACEAE) BASED ON NUCLEAR RIBOSOMAL ITS AND ETS SEQUENCES
Figure 5. Ancestral area reconstruction produced by means of the RASP–Bayesian binary Markov Chain Monte Carlo method and based on the occurrence of Verbesina L. (Heliantheae–Asteraceae) species. Nodes with a predicted dispersal component are circled in blue, and those with a significant vicariance component are circled in green. The green bar indicates the consensus age of the closure of the Panama Isthmus (age based on Leigh et al., 2013; O'Dea et al., 2016). BOL, Bolivia; BRA, Brazil; CAR, Caribbean; COL, Colombia; CRC, Costa Rica; ECU, Ecuador; MEX, Mexico; NIC, Nicaragua; PER, Peru; USA, United States of America; VEN, Venezuela.
Figure 4 in A TIME-CALIBRATED PHYLOGENY OF VERBESINA (HELIANTHEAE - ASTERACEAE) BASED ON NUCLEAR RIBOSOMAL ITS AND ETS SEQUENCES
Figure 4. Time-calibrated Bayesian inference tree generated using concatenated internal and external transcribed spacer data. The values at the nodes indicate mean divergence dates, and the horizontal bars indicate 95% highest posterior density ranges for the age at each node. The green bar indicates the consensus age of the closure of the Panama Isthmus (age based on Leigh et al., 2013; O'Dea et al., 2016). BOL, Bolivia; BRA, Brazil; CAR, Caribbean; COL, Colombia; CRC, Costa Rica; ECU, Ecuador; MEX, Mexico; NIC, Nicaragua; PER, Peru; USA, United States of America; VEN, Venezuela.
Figure 3 in A TIME-CALIBRATED PHYLOGENY OF VERBESINA (HELIANTHEAE - ASTERACEAE) BASED ON NUCLEAR RIBOSOMAL ITS AND ETS SEQUENCES
Figure 3. Bayesian inference tree of combined internal and external transcribed spacer data. Posterior probabilities> 0.9 are given above the branches. The red text indicates South American species. Leaf figures indicate opposite and alternate phyllotaxy. Chromosome numbers are based on Moreira & Cavalcanti (2020) and Panero & Strother (2021). BOL, Bolivia; BRA, Brazil; CAR, Caribbean; COL, Colombia; CRC, Costa Rica; ECU, Ecuador; MEX, Mexico; NA, North America; NIC, Nicaragua; PER, Peru; SA, South America; VEN, Venezuela.
Figure 2 in A TIME-CALIBRATED PHYLOGENY OF VERBESINA (HELIANTHEAE - ASTERACEAE) BASED ON NUCLEAR RIBOSOMAL ITS AND ETS SEQUENCES
Figure 2. Total distribution of Verbesina in North America, Central America, the Caribbean, and South America. (Data accessed from GBIF, https://www.gbif.org/).
Figure 1 in A TIME-CALIBRATED PHYLOGENY OF VERBESINA (HELIANTHEAE - ASTERACEAE) BASED ON NUCLEAR RIBOSOMAL ITS AND ETS SEQUENCES
Figure 1. Morphological characters in Verbesina. A, Tree of Verbesina floribunda Gardner; B, subshrubby habit of V. bipinnatifida Baker; C, capitulum of V. luetzelburgii Mattf.; D, capitulum of V. bipinnatifida; E, cypsela of V. bipinnatifida; F, cypsela of V. floribunda; G, scanning electron micrograph (SEM) of the verrucous cypsela surface of V. macrophylla (Cass.) S.F.Blake; H, inflorescence of V. macrophylla; I, pinnatipartite leaf of V. macrophylla; J, SEM of the scalariform cypsela surface of V. glabrata Hook. & Arn.; K, inflorescence of V. glabrata; L, entire leaf of V. glabrata. Vouchers: C, G.L. Moreira et al. 118 (CEN); D–E, G.L. Moreira et al. 116 (CEN); F, G.L. Moreira et al. 101 (CEN). Scale bars: C, 8 mm; D, 4 mm; E, 2 mm; F, 4 mm; G and J, 200 μm. Photographs: G. L. Moreira.
Fig. 2c. Tillomorphites otiliae n in Two new fossil species of Tillomorphites Vitali (Coleoptera: Cerambycidae) and remarks on the morphological evolution, mimicry, biogeography and phylogeny of the tribe Tillomorphini
Fig. 2c. Tillomorphites otiliae n. sp., habitus, Fig. 2 e. Tillomorphites otiliae n. sp., reconstruction. Paratype, colour reconstruction.
FIGURE 4 in One step closer but still far from solving the puzzle - The phylogeny of marine associated mites (Acari, Oribatida, Ameronothroidea) inferred from morphological and molecular genetic data
FIGURE 4 Bayesian inference topology based on 66 morphological traits of 102 oribatid mite species. Posterior probability values are shown near nodes. Photographs of selected species are given to provide an insight into the basic morphology of each larger group. *Photograph shows Tegeocranellus knysnaensis, this species was not used for the analyses but is given here to visualize the typical habitus of Tegeocranellus species.
FIGURE 3 in One step closer but still far from solving the puzzle - The phylogeny of marine associated mites (Acari, Oribatida, Ameronothroidea) inferred from morphological and molecular genetic data
FIGURE 3 One of 14 most parsimonious trees based on 66 characters or character states of 98 ameronothroid and four terrestrial oribatid mite species. Bootstrap values are shown near nodes. Colours refer to different families and are the same as in preceding figures.
FIGURE 1 in One step closer but still far from solving the puzzle - The phylogeny of marine associated mites (Acari, Oribatida, Ameronothroidea) inferred from morphological and molecular genetic data
FIGURE 1 Bayesian inference tree of marine associated Ameronothroidea and terrestrial outgroups based on 18S sequences. Posterior probabilities>0.9 are shown near nodes; abbreviations: PRT – Portugal, DE – Germany, DR – Dominican Republic, JP – Japan, TW – Taiwan, MY – Malaysia; families are given in different colours. Photographs of selected species are given to provide an insight into the basic habitus of each larger group.
FIGURE 2 in One step closer but still far from solving the puzzle - The phylogeny of marine associated mites (Acari, Oribatida, Ameronothroidea) inferred from morphological and molecular genetic data
FIGURE 2 Bayesian topology based on the combined data set of coi, D3 and 18S sequences. Posterior probabilities>0.9 are shown near nodes; abbreviations: PRT – Portugal, DE – Germany, DR – Dominican Republic, TW – Taiwan.
Fig 11. Capsicum neei Barboza & X in Four new species of Capsicum (Solanaceae) from the tropical Andes and an update on the phylogeny of the genus
Fig 11. Capsicum neei Barboza & X. Reyes. (A) Plant. (B) Flower bud. (C) Flowering branch. Photos by G. E. Barboza. https://doi.org/10.1371/journal.pone.0209792.g011
Fig 10. Capsicum neei Barboza & X in Four new species of Capsicum (Solanaceae) from the tropical Andes and an update on the phylogeny of the genus
Fig 10. Capsicum neei Barboza & X. Reyes. (A) Flowering branch. (B) Inflorescence. (C) Flower bud. (D) Flower. (E) Calyx. (F) Opened corolla. (G) Gynoecium (H) Fruit. (I) Glandular trichome of the inside calyx. (J) Glandular trichome of the pedicels. (K)
Fig 6 in Four new species of Capsicum (Solanaceae) from the tropical Andes and an update on the phylogeny of the genus
Fig 6. Bayesian majority-rule consensus tree of Capsicum. Posterior probabilities values indicated by each branch. New species are highlighted in bold-colored letters and the clade to which they belong is indicated. https://doi.org/10.1371/journal.pone.0209792.g006
Fig 5 in Multigene phylogeny reveals a new Iranian earthworm genus (Lumbricidae: Philomontanus) with three new species
Fig 5. Sampling sites of new species. (A1, A2) Mazandaran, Abbasabad (36.72 o N; 51.11o E), Elburz Mountains, sampling site of Philomontanus sarii sp. nov. (B1, B2) Kurdistan, Kamyaran (35.49o N; 46.35o E), Zagros Mountains, sampling site of Philomontanus baloutchi sp. nov. (C1, C2) Kurdistan, Baneh (35.99o N; 45.88o E), Zagros Mountains, sampling site of Philomontanus mahmoudi sp.nov. https://doi.org/10.1371/journal.pone.0208904.g005
Fig 3 in Multigene phylogeny reveals a new Iranian earthworm genus (Lumbricidae: Philomontanus) with three new species
Fig 3. Ventrolateral view of the Philomontanus species. Arrows point to tubercula pubertatis A. Philomontanus sarii sp. nov. B. Philomontanus mahmoudi sp. nov. C. Philomontanus baloutchi sp. nov.. https://doi.org/10.1371/journal.pone.0208904.g003
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.