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154 results for “Raja”
Figure 4 from: Medina-Ortiz AJ, Herrera T, Vásquez-Dávila MA, Raja HA, Figueroa M (2017) The genus Podaxis in arid regions of Mexico: preliminary ITS phylogeny and ethnomycological use. MycoKeys 20: 17-36. https://doi.org/10.3897/mycokeys.20.11570
Figure 4 - Phylogram of the most likely tree (-lnL = 1860.99) from a RAxML analysis of 56 taxa based on ITS rDNA (681 bp). Numbers above the nodes refer to RAxML bootstrap support values ≥ 70% based on 1000 replicates. Clades to the right (A–F) are labeled as per Conlon et al. 2016. The tree is rooted with Leucocoprinus birnbaumii. Symbol (*) next to collections indicates, it was reported from termite mounds. Bar indicates nucleotide substitutions per site.
Figure 2 from: Medina-Ortiz AJ, Herrera T, Vásquez-Dávila MA, Raja HA, Figueroa M (2017) The genus Podaxis in arid regions of Mexico: preliminary ITS phylogeny and ethnomycological use. MycoKeys 20: 17-36. https://doi.org/10.3897/mycokeys.20.11570
Figure 2 - Fruit bodies and basidiospores of selected Podaxis specimens from clades D (MEXU 12808 and 27557) and E (MEXU 8424 and 8426).
Figure 3 from: Medina-Ortiz AJ, Herrera T, Vásquez-Dávila MA, Raja HA, Figueroa M (2017) The genus Podaxis in arid regions of Mexico: preliminary ITS phylogeny and ethnomycological use. MycoKeys 20: 17-36. https://doi.org/10.3897/mycokeys.20.11570
Figure 3 - Mean ± SE spore (A) length and (B) width of MEXU Podaxis specimens from clades D and E. Results of Mann-Whitney U test: D–E, p < 0.001.
FIGURE A7 A–B in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia
FIGURE A7 A–B. Faunus ater (L = 35.8 mm, W = 8.7 mm), C–D. Terebralia palustris (L = 56.1 mm, W = 22.5 mm), E–F. Terebralia sulcata (L = 37.8 mm, W = 19.7 mm), G. Cypraea tigris, H. Monetaria annulus. Scale bars: 5 mm.
FIGURE A5 A in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia
FIGURE A5 A. Spondylus sp., B. Chama Lazarus, C–D. Chama limbula (L = 62.8 mm, H = 49.8 mm), E-F. Geloina papua, juvenile (L = 26.6 mm, H = 41.4 mm), G. Aphrodora sp. (L = 16.4 mm, H = 1.3 mm). Scale bars: 5 mm, unless stated otherwise.
FIGURE 4 in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia
FIGURE 4 Non-metric Multidimensional Scaling (NMDS) ordination plot of mollusc assemblages from 11 marine lakes in Raja Ampat, Indonesia, based on Jaccard distances between lakes. Mollusc species that have significant influence on reshaping the species composition among marine lakes are shown Geloina papua (r2 = 0.78, P = 0.02), Brachidontes sp. (r2 = 0.78, P = 0.02), Brachidontes ustulatus (r2 = 0.66, P = 0.018), Cerithium coralium (r2 = 0.59, P = 0.017), Neocollonia pilula (r2 = 0.56, P = 0.044) and Terebralia palustris (r2 = 0.63, P = 0.024). The arrows represent environmental (temperature and salinity) and physical characteristics (connectivity and surface area) of the lakes.
FIGURE 1 in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia
FIGURE 1 Map of sampling locations in Raja Ampat, West Papua, Indonesia. (A) Overview of Indonesia. (B) Close-up of Misool, Raja Ampat, including 11 marine lakes. (C) Aerial and (D) ground level views of a marine lake. (E) Categorization of sampling areas according to the degree of connection into three groups: High, Medium and Low. Location codes and connectivity measurements correspond with table 1. Downloaded from Brill.com 06/21/2024 06:27:04PM via Open Access. This is an open access article distributed under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/
FIGURE 19. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 19. Rajella lintea mature male, ZMH 113180, radiograph of pelvic girdle.
FIGURE 18. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 18. Rajella lintea mature male, ZMH 113180, radiograph of cranium and snout.
FIGURE 3. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 3. Rajella lintea mature male, ZMH 113180, mouth-nasal region in ventral view.
FIGURE 4. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 4. Rajella lintea mature male, ZMH 113180, pelvic-clasper region in dorsal view.
FIGURE 8. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 8. Rajella lintea mature male, ZMH 113180, right side alar thorn field.
FIGURE 2. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 2. Rajella lintea mature male, ZMH 113180, dorsal fins and tail end in semilateral view.
FIGURE 7. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 7. Rajella lintea mature male, ZMH 113180, thorns on origin of tail dorsally.
FIGURE 6. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 6. Rajella lintea mature male, ZMH 113180, mid-section of tail in dorsal view.
FIGURE 1. Rajella lintea mature male, ZMH 113180 in Complementary redescription of Raja lintea Fries, 1839 (Elasmobranchii, Rajidae) and its revised generic assignment
FIGURE 1. Rajella lintea mature male, ZMH 113180, in total dorsal (a) and ventral (b) views.
Figures 4a- b from: Raja H, Schoch C, Hustad V, Shearer C, Miller A (2011) Testing the phylogenetic utility of MCM7 in the Ascomycota. MycoKeys 1: 63-94. https://doi.org/10.3897/mycokeys.1.1966
Figures 4a- b - Nucleotide substitution saturation plots: The proportion of transitions (s) and transversions (v) were plotted against sequence divergence using Jukes-Cantor evolutionary distance in the program DAMBE.
Figure 6 from: Raja H, Schoch C, Hustad V, Shearer C, Miller A (2011) Testing the phylogenetic utility of MCM7 in the Ascomycota. MycoKeys 1: 63-94. https://doi.org/10.3897/mycokeys.1.1966
Figure 6 - Phylogenetic informativeness profiles for two genes LSU (1076 bp) and MCM7 (642 bp) through 1.4 time units using PhyDesign online tool. Tree was obtained with PHYML. The relative time units are shown on the X-axis and profiles of net and per-site phylogenetic informativeness is shown on the Y-axis. Profiles of LSU gene are shown in red and MCM7 are shown in green.
Figure 2 from: Raja H, Schoch C, Hustad V, Shearer C, Miller A (2011) Testing the phylogenetic utility of MCM7 in the Ascomycota. MycoKeys 1: 63-94. https://doi.org/10.3897/mycokeys.1.1966
Figure 2 - Maximum Likelihood phylogeny of Leotiomyceta (Ascomycota) based on MCM7 data set (642 bp) of 89 taxa using PhyML ((-ln)L score 24325). Support values, shading and classification as in Fig. 1.
Figure 3 from: Raja H, Schoch C, Hustad V, Shearer C, Miller A (2011) Testing the phylogenetic utility of MCM7 in the Ascomycota. MycoKeys 1: 63-94. https://doi.org/10.3897/mycokeys.1.1966
Figure 3 - Maximum Likelihood phylogeny of Leotiomyceta (Ascomycota) based on a combined 28S nrDNA large subunit and MCM7 data set (1718 bp) of 89 taxa using PhyML ((-ln)L score 39965). Support values, shading and classification as in Fig. 1.
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