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FIGURES 34a–f in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 34a–f. Tephritis tridentata: a—tip of aculeus, ventral view; b—eversible membrane, ventral view; c—aculeus, ventral view; d—spermathecae; e—glans of phallus, lateral; f—epandrium, posterior view. Scale bar = 1 mm.
FIGURES 4a–g in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 4a–g. Tephritis arsenii: a—habitus ♀; b—wing; c—glans of phallus, lateral; d—tip of aculeus, ventral view; eaculeus, ventral view; f—spermathecae; g—eversible membrane, ventral view. Scale bar = 1 mm, e = 0.5 mm.
FIGURES 3a–h in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 3a–h. Tephritis, spp. wings: a—T. truncata; b—T. stictica; c—T. arsenii; d—T. arsenii (paratype); e—T. ruralis; f— T. tridentata; g—T. conyzifoliae; h—T. crepidis. Scale bar = 1 mm.
Fig. 4 in Sex or no sex? Group I introns and independent marker genes reveal the existence of three sexual but reproductively isolated biospecies in Trichia varia (Myxomycetes)
Fig. 4 Simplified SSU phylogeny showing distribution of IC1 and IE class introns at position S956 in myxomycetes. Tree topology was derived from published SSU phylogenies (Fiore-Donno et al. 2010, 2012, 2013) and the tree presented in Supplementary Fig. S1 of this study. Trichia varia group 1 is represented by a specimen with an intron lacking an HEG; group 2a is represented by a specimen with a HEG-containing intron. Taxa printed in red and marked with "IC1" carry IC1 introns; those printed in blue and marked with "IE" carry IE introns. Nodes marked by dots received support of both Bayesian posterior probability>0.70 and bootstrap replicates>50 (Color figure online)
Fig. 3 in Sex or no sex? Group I introns and independent marker genes reveal the existence of three sexual but reproductively isolated biospecies in Trichia varia (Myxomycetes)
Fig. 3 Intron types found in 66 specimens of Trichia varia at six insertion positions. For each of the phylogroups 1 and 2a, introns are drawn to scale as horizontal bars. White sections denote intron sequences and gray sections homing endonuclease genes. Red/solid and
Fig. 2 in Geographical versus ecological isolation of closely related black flies (Diptera: Simuliidae) inferred from phylogeny, geography, and ecology
Fig. 2 Principal components analysis (PCA) of stream variables for four species in Clade I-1 of subgenus Gomphostilbia in Thailand. Factor score 1 (PC-1) explained 33.75 % of the total variation and was related positively to stream width, depth, velocity, pH, and conductivity and negatively to altitude. Factor score 2 (PC-2) explained 26.76 % of the total variation and was positively related to stream width, depth, and velocity and negatively to pH and conductivity. The four taxa of Clade I-1 were separated in environmental space along the two axes
Fig. 3 in A new rodent species of the genus Mus (Rodentia: Muridae) confirms the biogeographical uniqueness of the isolated forests of southern Ethiopia
Fig. 3 Posterior sample of species trees from STACEY over- laid by MCC tree. The analysis is based on six nuclear loci. Classification to the maximum credibility MSC species set is indicated on the right margin with colours indicating cor- respondence to CYTB lineages. Branch labels show gdi values of the maximum credibility MSC species consisting of more than one individual
Fig. 1 in A new rodent species of the genus Mus (Rodentia: Muridae) confirms the biogeographical uniqueness of the isolated forests of southern Ethiopia
Fig. 1 (A) and (B) Summary of the distribution of native Ethiopian species of the genus Mus (i.e. excluding introduced commensal M. musculus) based on genetically confirmed records. The taxonomy follows Bryja et al. (2014). Selected major potential natural vegetation types in Ethiopia (based on Lillesø et al., 2011), relevant for this study, are shown by different background colours: Afromontane rain forests (green), Afroalpine vegetation and montane Ericaceous belt (light grey). The rest of background in the scale of grey indicates elevation (higher is darker). The records of DNA-barcoded specimens of eight species are shown by different symbols. More details (e.g. GPS coordinates and GenBank accession numbers) are in Supplementary Information 1. Mus harennensis sp. nov. is distributed only in two very moist rain forests, Harenna and Chingawa; Mus mahomet is widespread species across the Ethiopian Highlands; Mus proconodon is found at low elevation in savannah-like habitats; Mus imberbis is an Afroalpine specialist, easily distinguished by external mor-
Fig. 6 Wireframe plots showing skull form difference between M in A new rodent species of the genus Mus (Rodentia: Muridae) confirms the biogeographical uniqueness of the isolated forests of southern Ethiopia
Fig. 6 Wireframe plots showing skull form difference between M. triton (blue) and M. sp. "Harenna" (red). The uppermost panel shows size difference by scaling of dorsal consensus configuration, the other three show shape differences in three views of the skull. The most significant difference is highlighted in the lowermost panel (ventral view). See Supplementary Information 3 (Fig. S3.1) for the anatomical location of landmarks
FIGURE 1 in Biscogniauxia dicranopteridis sp. nov. and B. petrensis isolated from Dicranopteris dichotoma in China
FIGURE 1. Phylogenetic tree generated from maximum likelihood analysis of a combined LSU, ITS, RPB2 and β-TUB sequence dataset. Bootstrap support values for ML and MP of at least 75% and Bayesian posterior probabilities of at least 0.95 are shown near the nodes as ML/PP/MP. The tree is rooted with Hypoxylon pulicicidum (MUCL49879) and H. rickii (MUCL53309). The newly generated strains are shown in red. Ex-type strains are indicated in bold.
FIGURE 6 in Two new endophytic fungi of Colletotrichum and Diaporthe isolated from Berchemia polyphylla var. leioclada in Guizhou Province, China
FIGURE 6. Results of the PHI test of Diaporthe berchemiae and closely related species using both LogDet transformation and splits decomposition. The PHI test results (Φw) <0.05 indicate significant recombination within the dataset. The new taxa are in red.
FIGURE 1 in Tubakia byeongjinii, a new species of Tubakiaceae, isolated from Quercus variabilis in South Korea
FIGURE 1. Phylogenetic relationship between Tubakia byeongjinii isolates and some reference isolates retrieved from the NCBI database, inferred by the maximum likelihood method using a combined data set of the LSU, ITS, and TEF-1α gene regions. Bootstrap values (≥50%) based on 1000 replications are indicated. The scale bar represents 0.01 nucleotide substitutions per site. The isolates used in this work are indicated in bold.
Targeted isolation of bacteria with potential to competitively exclude Staphylococcus aureus in the upper respiratory tract of pigs
<p>Data to support a publication</p>
Table 1 in Antioxidant and anticholinesterase potential of Ferulago cassia with farther bio-guided isolation of active coumarin constituents *
<p><b>Table 1</b> Sums of the crushed aerial parts, roots, flowers and fruits and gained extracts and fractions.</p><table><tbody><tr><th>Species</th><th>Extracts/Fractions</th><th>Aerial part</th><th>Root</th><th>Flower</th><th>Fruit</th></tr></tbody><tbody><tr><th><i>Ferulago cassia</i></th><td>MeOH (g)</td><td>32.12</td><td>30.02</td><td>26.93</td><td>29.77</td></tr><tr><td>Hexane (g)</td><td>3.69</td><td>2.37</td><td>3.38</td><td>3.40</td></tr><tr><td>CH2Cl2 (g)</td><td>11.91</td><td>15.01</td><td>9.82</td><td>10.18</td></tr><tr><td>EtOAc (g)</td><td>2.76</td><td>2.28</td><td>1.96</td><td>2.54</td></tr><tr><td>BuOH (g)</td><td>5.99</td><td>4.55</td><td>4.51</td><td>6.08</td></tr><tr><td>Aqueous residue (g)</td><td>6.92</td><td>5.69</td><td>6.30</td><td>6.23</td></tr><tr><td>Lyophilized aqueous (g)</td><td>4.74</td><td>3.98</td><td>4.87</td><td>5.56</td></tr></tbody></table>
Marine Planctomycetota isolated from the biofilm surface of Fucus spiralis
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FIGURE A1 in Abelisauridae (Dinosauria: Theropoda) from the Late Jurassic of Portugal and dentition-based phylogeny as a contribution for the identification of isolated theropod teeth
FIGURE A1. Cross-section outlines of the base crown at the cervix in nonavian theropods. A. subcircular; B. elliptical; C. subrectangular; D. oval; E. lanceolate; F. lenticular; G. eight-shaped; H. bean-shaped (reniform); I–J. U-shaped; K–L. Dshaped; M–N. 'Flying-saucer' shape; O. J-shaped.
FIGURE A8. A in Abelisauridae (Dinosauria: Theropoda) from the Late Jurassic of Portugal and dentition-based phylogeny as a contribution for the identification of isolated theropod teeth
FIGURE A8. A. Strict consensus cladogram of nine most parsimonious trees recovered from the analysis of a supermatrix including a dentition-based datamatrix and six recent datasets based on whole theropod skeleton (i.e., Xu et al. 2009; Brusatte et al. 2010; Martinez et al. 2011; Senter 2011; Pol and Rauhut 2012; Carrano et al. 2012). Initial analysis was a New Technology Search using TNT v.1.1 of a supermatrix comprising 1972 characters for one outgroup (Eoraptor) and 59 nonavian theropod taxa. Tree length = 3583 steps; CI = 0.546; RI = 0.604. B. Strict consensus cladogram of four most parsimonious trees recovered from the analysis of a supermatrix after the deletion of the two wildcard taxa Erectopus and Piatnitzkysaurus. Tree length = 3529 steps; CI = 0.575; RI = 0.642.
FIGURE 5 in Abelisauridae (Dinosauria: Theropoda) from the Late Jurassic of Portugal and dentition-based phylogeny as a contribution for the identification of isolated theropod teeth
FIGURE 5. Plots of CBR versus CHR of ML 962, ML 327, ML 966 and 23 theropod taxa comprising the data set. For reasons of clarity, only taxa with CBR of less than 1 were considered.
FIGURE A10 in Abelisauridae (Dinosauria: Theropoda) from the Late Jurassic of Portugal and dentition-based phylogeny as a contribution for the identification of isolated theropod teeth
FIGURE A10. Strict consensus cladogram of 96 most parsimonious trees recovered from the analysis of a supermatrix including a dentition-based datamatrix and six recent datasets based on whole theropod skeleton (i.e., Xu et al. 2009; Brusatte et al. 2010; Martinez et al. 2011; Senter 2011; Pol and Rauhut 2012; Carrano et al. 2012). Initial analysis was a New Technology Search using TNT v.1.1 of a supermatrix comprising 1972 characters for one outgroup (Eoraptor), 59 non-avian theropod taxa and ML 327, ML 966, ML 939 (coded as lateral teeth), and ML 962 (coded as a mesialmost tooth). Tree length = 3607 steps; CI = 0.529; RI = 0.58.
FIGURE 3 in Plastid DNA fingerprinting of the rare Fritillaria moggridgei (Liliaceae) reveals population differentiation and genetic isolation within the Fritillaria tubiformis complex
FIGURE 3. Median-joining (MJ) network for the combined plastid DNA data set of Fritillaria tubiformis s.l. A. MJ network based on indel repeats at locus 4, 7, 8, 9, 10. Haplotypes (Ha, Hb1 and Hb2) are indicated by circles, the size of each circle being proportional to the observed frequency of each haplotype. B. MJ network for the combined plastid DNA data set of Fritillaria tubiformis s.l. based on all ten microsatellites. Median vectors are labelled mv1, mv2, mv3 and mv4. Number of changes required to explain transitions among haplotypes is indicated along the lines of the networks, except for connections that required only a single change. Information on type and number of repeat motifs contributing to the network is provided for the two main clusters (A and B) corresponding to var. burnatii and subsp. moggridgei.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.
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