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2,620 results for “Molecular Phylogeny”
Figure 5 in A molecular phylogeny of Equatorial African Lacertidae, with the description of a new genus and species from eastern Democratic Republic of the Congo
Figure 5. Map of the Itombwe Plateau, showing collection localities for Congolacerta asukului sp. nov. (open squares). The type locality is indicated by a star symbol.
Figure 1 in A molecular phylogeny of Equatorial African Lacertidae, with the description of a new genus and species from eastern Democratic Republic of the Congo
Figure 1. Maximum likelihood phylogeny (RAxML tree) of lacertid lizards in the Equatorial African Group, based on the combined nuclear c-mos (oocyte maturation factor)/RAG1 (recombination activating gene 1) data set from this study and GenBank samples from Mayer & Pavlicev (2007). Bootstrap and posterior probability values for each well-supported node are listed in the order: maximum parsimony/maximum likelihood/Bayesian inference.
Figure 7 in A molecular phylogeny of Equatorial African Lacertidae, with the description of a new genus and species from eastern Democratic Republic of the Congo
Figure 7. Dorsal views of the heads of Congolacerta asukului sp. nov. (holotype, UTEP 20263) and Congolacerta vauereselli (UTEP 20291). Supraciliary granules are shaded in grey. Scale bars = 1 mm.
Figure 6 in A molecular phylogeny of Equatorial African Lacertidae, with the description of a new genus and species from eastern Democratic Republic of the Congo
Figure 6. Photograph of the type locality of Congolacerta asukului sp. nov., showing grassland habitat with rocky outcrops.
Figure 3 in A molecular phylogeny of Equatorial African Lacertidae, with the description of a new genus and species from eastern Democratic Republic of the Congo
Figure 3. Photographs of Congolacerta in life. Dorsal (A) and ventral (B) view of Congolacerta asukului holotype UTEP 20263 [adult male, 58.3 mm snout–vent length (SVL)], dorsal view (C) of C. asukului paratype UTEP 20265 (adult male, 53.7 mm SVL), dorsal view (D) of C. asukului paratype UTEP 20267 (subadult male, 42.7 mm SVL), and dorsal (E) and ventral (F) view of Congolacerta vauereselli UTEP 20289 (adult male, 54.4 mm SVL).
Figure 4 in A molecular phylogeny of Equatorial African Lacertidae, with the description of a new genus and species from eastern Democratic Republic of the Congo
Figure 4. Photographs of the holotype of Congolacerta asukului sp. nov. (UTEP 20263, adult male, 58.3 mm snout–vent length) after preservation. Dorsal (A) and ventral (B) view of whole specimen, lateral (C), dorsal (D), and ventral (E) view of head, and ventral view of cloacal region (F) illustrating femoral pores. Scale bars = 0.5 cm.
Figure 2 in A molecular phylogeny of Equatorial African Lacertidae, with the description of a new genus and species from eastern Democratic Republic of the Congo
Figure 2. Maximum likelihood phylogeny (RAxML tree) of the Equatorial African clade of lizards based on the combined 16S, cytochrome b (cyt b), c-mos, and RAG1 genes. Bootstrap and posterior probability values for each well-supported node are listed in the order: maximum parsimony/maximum likelihood/Bayesian inference.
Figure 3 in Molecular phylogeny and classification of the chemosymbiotic bivalve family Lucinidae (Mollusca: Bivalvia)
Figure 3. Molecular phylogeny of the Lucinidae based on the single gene analysis of cytochrome b produced by Bayesian analysis using MRBAYES. Support values are Bayesian posterior probabilities (%). Details of taxa are given in Table 1.
Figure 2 in Molecular phylogeny and classification of the chemosymbiotic bivalve family Lucinidae (Mollusca: Bivalvia)
Figure 2. Molecular phylogeny of the Lucinidae based on the single gene analysis of 28S rRNA produced by Bayesian analysis using MRBAYES. Support values are Bayesian posterior probabilities (%). Details of taxa are given in Table 1.
Figure 1 in Molecular phylogeny and classification of the chemosymbiotic bivalve family Lucinidae (Mollusca: Bivalvia)
Figure 1. Molecular phylogeny of the Lucinidae based on the single gene analysis of 18S rRNA produced by Bayesian analysis using MRBAYES. Support values are Bayesian posterior probabilities (%). Details of the taxa are given in Table 1.
Figure 1 in Molecular phylogeny of the Forcipulatacea (Asteroidea: Echinodermata): systematics and biogeography
Figure 1. Forcipulatacean diversity. Preserved specimens from the USNM collections; images by C. Mah, unless otherwise noted. A, Pisaster ochraceus E01663 (boreal-clade Asteriidae) B, Diplasterias brandti 1121889, showing brooded juveniles (Antarctic-clade Asteriidae), image courtesy of Adrian Testa, USARP. C, Coscinasterias tenuispina E10146 (pantropical-clade Asteriidae). D, Sclerasterias mollis E09987 (Sclerasterias-clade Asteriidae). E, Labidaster annulatus (Heliasterid/Labidiasteridae). F, Heliaster multispinus E45326 (Heliasteridae). G, Zoroaster fulgens USNM 1017683 (Zoroasteridae). H, Novodinia antillensis (Brisingida), image courtesy of Sandra Brooke, MCBI. I, Stichaster striatus 1082892 (Stichasterid clade). Scale bar: 1.0 cm.
Figure 3. Maximum-likelihood tree for 78 in Molecular phylogeny of the Forcipulatacea (Asteroidea: Echinodermata): systematics and biogeography
Figure 3. Maximum-likelihood tree for 78 forcipulate taxa and five velatidan taxa, based on 327 bp for the early-stage histone H3 gene plus the same rDNA sequences that were used in Figure 2. Bootstrap support values are based on 200 pseudoreplicates. Other details are as described in Figure 2.
Figure 3 in The flightless marine midge Pontomyia (Diptera: Chironomidae): ecology, distribution, and molecular phylogeny
Figure 3. Maximum likelihood tree from four-gene analysis as performed in GARLI. The three values on each branch represent: (1) maximum likelihood bootstrap support; (2) Bayesian posterior probability (PP); and (3) maximum parsimony bootstrap support. Key: *bootstrap value> 98 or PP of 1; #maximum likelihood and maximum parsimony bootstrap values> 98 and PP of 1.
Figure 2 in The flightless marine midge Pontomyia (Diptera: Chironomidae): ecology, distribution, and molecular phylogeny
Figure 2. Photomicrographs showing the male hypogium of each Pontomyia species. A, Pontomyia natans from type series. B, Pontomyia pacifica P06 from Palau. C, Pontomyia cottoni from type series. D, Pontomyia oceana P25 from Taiwan. The scale bar at the bottom right applies to all panels.
Figure 4 in The flightless marine midge Pontomyia (Diptera: Chironomidae): ecology, distribution, and molecular phylogeny
Figure 4. Species tree obtained from BEST analysis of multilocus data. The value on each branch represents the Bayesian posterior probability.
Figure 1 in The flightless marine midge Pontomyia (Diptera: Chironomidae): ecology, distribution, and molecular phylogeny
Figure 1. Map showing the known collection sites of Pontomyia species:, Pontomyia natans; Δ, Pontomyia pacifica; Z, Pontomyia cottoni; O, Pontomyia oceana;, Atlantic Pontomyia sp. (filled symbols indicate type localities). Note that P. natans co-occur with P. pacifica at the type locality of the latter, whereas P. natans and P. oceana co-occur in southern Taiwan.
Figure 36. A in Molecular phylogeny in endemic weevils: revision of the genera of Macaronesian Cryptorhynchinae (Coleoptera: Curculionidae)
Figure 36. A, Silvacalles nubilosus (in dorsal view). B, aedeagus in ventral view (left), endophallus (right). C, Ixanthus viscosus Griseb., the host plant of S. nubilosus.
Figures 33–34 in Molecular phylogeny in endemic weevils: revision of the genera of Macaronesian Cryptorhynchinae (Coleoptera: Curculionidae)
Figures 33–34. Sonchiacalles muelleri has the same larval development, the adults show identical breeding behaviour and the larvae and pupae behave in the same way in the chambers (made of latex and agglutinated small stones) at the root neck of, e.g. Tolpis proustii on El Hierro as Madeiracalles pulverosus in the roots of Tolpis succulenta on Madeira.
Figures 25–32. 25–27 in Molecular phylogeny in endemic weevils: revision of the genera of Macaronesian Cryptorhynchinae (Coleoptera: Curculionidae)
Figures 25–32. 25–27, Madeiracalles is distinguished from the Canarian genera by the conspicuously long and slender, capillary bristles on the median lobe of the aedeagus. 28–32, the 'complex' inverse v-shaped structure of the endophallus shows a clearly comprehensible basic pattern and is doubtlessly homologous amongst the species of Madeiracalles.
Figures 2–22 in Molecular phylogeny in endemic weevils: revision of the genera of Macaronesian Cryptorhynchinae (Coleoptera: Curculionidae)
Figures 2–22. Morphological, biological, and ecological comparison of the genera and subgenera of Macaronesian Cryptorhynchinae along with the respective sections of the tree; (TS) = type species. Figures 4E and 5E show a section of the tree that results when 16S sequences for Aeoniacalles aeonisimilis* and Dendroacalles euphorbiacus* are excluded.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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