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501 results for “phylogenetic taxonomy”
FIGURE 2 in Phylogenetic position, taxonomy, distribution, and conservation status of the rare and poorly-known Noccaea rosularis, the generic type of Masmenia (Brassicaceae)
FIGURE 2. Phylogenetic placement of Noccaea rosularis (Masmenia rosularis) in Tribe Coluteocarpeae, based on Bayesian analysis of ITS data. Posterior probability (PP) values> 0.5 are shown at nodes. Taxon names follow concept presented in Brassibase (https:// brassibase.cos.uni-heidelberg.de/).
FIGURE 4 in Phylogenetic position, taxonomy, distribution, and conservation status of the rare and poorly-known Noccaea rosularis, the generic type of Masmenia (Brassicaceae)
FIGURE 4. Fruit and seeds of Noccaea rosularis. A. Septum and seed position under light microscope (LM); B. Seed shape and colour under LM; C. SEM general appearance of seed; D. SEM detail of testa surface. Scale bars (A–B) = 1 mm.
FIGURE 3. Noccaea rosularis. A, D in Phylogenetic position, taxonomy, distribution, and conservation status of the rare and poorly-known Noccaea rosularis, the generic type of Masmenia (Brassicaceae)
FIGURE 3. Noccaea rosularis. A, D. Habit; B. Flowers; C. Basal leaves; E. Habitat; F. Fruit; G. Infructescence.
Table 6 in Taxonomy and molecular phylogenetic position of new species and new records of Coelosphaeridae (Demospongiae: Poecilosclerida) from the Mexican Pacific
<p><b>Table 6.</b> Distribution of polymorphic sites in the 28S DNAr region (C1–D2 domain) for four specimens of <i>L. (W.) hawaiiana</i>, one from Hawaii (Vicente <i>et al.</i> 2020) and three from the Mexican Pacific (this study)</p><table><tbody><tr><th><b><i>L.</i> (<i>W.</i>) <i>hawaiiana</i></b></th><th></th><th></th><th><b>Positions of mutations</b></th></tr></tbody><tbody><tr><th>Specimens</th><td><b>Locality</b></td><td><b>GenBank accession number</b></td><td>566</td><td>608</td><td>633</td></tr><tr><th><b>LEB-ICML-UNAM-2441</b></th><td>Playa la Concha, Baja California Sur</td><td>OP704020</td><td>T</td><td>-</td><td>T</td></tr><tr><th><b>LEB-ICML-UNAM-2447</b></th><td>Playa la Concha, Baja California Sur</td><td>OP704019</td><td>T</td><td>-</td><td>T</td></tr><tr><th><b>LEB-ICML-UNAM-3055</b></th><td>La Entrega, Oaxaca</td><td>OP704021</td><td>T</td><td>-</td><td>T</td></tr><tr><th><b>UF 3804</b></th><td>Hawaii</td><td>MT452537</td><td>C</td><td>G</td><td>-</td></tr></tbody></table>
Table 1 in Taxonomy and molecular phylogenetic position of new species and new records of Coelosphaeridae (Demospongiae: Poecilosclerida) from the Mexican Pacific
<p><b>Table 1.</b> List of references and GenBank accession numbers of sequences used in molecular analysis. The species names are referred to through the accession number in the tree topologies. Sequences generated in the present study are in bold</p><table><tbody><tr><th><b>Reference</b></th><th><b>GenBank accession number</b></th><th></th></tr><tr><th><b>28S</b></th><th><i>COI</i></th></tr></tbody><tbody><tr><th><b>Belinky</b> <i>et al.</i> <b>2012</b></th><td></td><td>HE591461</td></tr><tr><th><b>Erpenbeck</b> <i>et al.</i> <b>2007</b></th><td></td><td>EF519638, EF519639, EF519643, EF519640, EF519641</td></tr><tr><th><b>Hestetun</b> <i>et al.</i> <b>2016</b></th><td>LN870644</td><td></td></tr><tr><th><b>Idan</b> <i>et al.</i> <b>2018</b></th><td></td><td>KX866766</td></tr><tr><th><b>Medina</b> <i>et al.</i> <b>2001</b></th><td>AY026376</td><td></td></tr><tr><th><b>Morrow</b> <i>et al.</i> <b>2012</b></th><td>Hº379226, Hº379228, Hº379229, Hº379230, Hº379231</td><td>JF440339</td></tr><tr><th><b>Morrow</b> <i>et al.</i> <b>2019</b></th><td>KF017189</td><td>KF017195</td></tr><tr><th><b>Nichols 2005</b></th><td>AY561883</td><td></td></tr><tr><th><b>Núñez</b> <i>et al.</i> <b>2017</b></th><td></td><td>KY565309</td></tr><tr><th><b>Pérez</b> <i>et al.</i> <b>2006</b></th><td>Dº241773</td><td></td></tr><tr><th><b>Regueiras</b> <i>et al.</i> <b>2019</b></th><td></td><td>KY492550, KY492536, KY492520</td></tr><tr><th><b>Riesgo</b> <i>et al.</i> <b>2013</b></th><td></td><td>JX999092, JX999090</td></tr><tr><th><b>Rossi</b> <i>et al.</i> <b>2019</b></th><td></td><td>MK803199</td></tr><tr><th><b>Thacker</b> <i>et al.</i> <b>2013</b></th><td>KC869522, KC869546, KC869556, KC869564, KC869447, KC869468, KC869537, KC869541, KC869613, KC869624, KC869629, KC869449, KC869501, KC869603, KC869597, KC869478, KC869489, KC869512, KC869608, KC869561, KC869479, KC869529, KC869506, KC869649, KC869548, KC869515, KC869627, KC869509</td><td></td></tr><tr><th><b>Vargas</b> <i>et al.</i> <b>2012</b></th><td></td><td>HE611618, HE611608</td></tr><tr><th><b>Vargas</b> <i>et al.</i> <b>2015</b></th><td></td><td>LN850204, LN850229, LN850210, LN850247, LN850251, LN850248</td></tr><tr><th><b>Vicente</b> <i>et al.</i> <b>2020</b></th><td>MT452537</td><td></td></tr><tr><th><b>Wulff 2006</b></th><td></td><td>Dº133901, Dº133897</td></tr><tr><th>Present study</th><td><b>OP740700, OP740709, OP740710, OP704019, OP704020, OP704021</b></td><td><b>OP715763</b></td></tr><tr><th>GenBank direct submission</th><td></td><td>KJ620400, LT160711, AJ843890, LR655634, LR655638</td></tr></tbody></table>
Table 2 in Taxonomy and molecular phylogenetic position of new species and new records of Coelosphaeridae (Demospongiae: Poecilosclerida) from the Mexican Pacific
<p><b>Table 2.</b> Comparative data for the dimensions of the spicules (in µm) of the genus <i>Celtodoryx</i>, shass length × width; head diameter are given for megascleres and total length for arcuate isochelae and oxychaetes.Values in parentheses are means</p><table><tbody><tr><th><i>Celtodoryx species</i></th><th><b>Diactinal megascleres tylotes and strongyles (and derivates)</b></th><th><b>Arcuate isochelae</b></th><th><b>Oxychaetes</b></th></tr><tr><th><b><i>Celtodoryx chichiltik</i> sp. nov.</b></th></tr><tr><th><b>Holotype</b></th></tr></tbody><tbody><tr><th>LEB-ICML-UNAM-144</th><td>TYa: 195–(213.8)–225 × 2–(2.65)–3; 2.5–(3.8)–5</td><td>20–(28)–32.5</td><td>51–(65.5)–95</td></tr><tr><td>STb: 213–(243.5)–273 × 2.5–(4.3)–7.5</td><td></td><td></td></tr><tr><th><b>Paratypes</b></th></tr><tr><th>LEB-ICML-UNAM-161</th><td>TY: 197.5–(231.7)–261.5 × 3–(4.2)–5; 4.5–(5.4)–6.3</td><td>25–(28)–30</td><td>55–(71.3)–100</td></tr><tr><td>ST: 215–(264)–287.5 × 5.5–(7.1)–8</td><td></td><td></td></tr><tr><th>LEB-ICML-UNAM-172</th><td>TY: 180–(206)–237.5 × 2.5–(3)–4.5; 3–(4)–5</td><td>20–(25.8)–30</td><td>30–(62.8)–90</td></tr><tr><td>ST: 187.5–(226)–287.5 × 3.7–(5.5)–8</td><td></td><td></td></tr><tr><th>LEB-ICML-UNAM-260</th><td>TY: 150–(238.5)–275 × 2.5–(4.8)–5; 3.8–(5)–7.5</td><td>22.5–(24.3)–27.5</td><td>47.5–(64.8)–78</td></tr><tr><td>ST: 235–(248.2)–287.5 × 5–(6.4)–7.5</td><td></td><td></td></tr><tr><th>LEB-ICML-UNAM-292</th><td>TY:190–(221.6)–250 × 2.5–(2.9)–5; 3.7–(4.9)–7</td><td>20–(23.6)–25</td><td>40–(67)–80</td></tr><tr><td>ST: 220–(230)–252.5 × 5–(6.4)–7.5</td><td></td><td></td></tr><tr><th>LEB-ICML-UNAM-618</th><td>TY:210–(225)245 × 2.5–(3.3)–5; 3–(4.8)–6.3</td><td>22.5–(24.2)–7</td><td>57.5–(69)–77.5</td></tr><tr><td>ST: 212.5–(228.3)–250 × 3–(3–8)–5</td><td></td><td></td></tr><tr><th>LEB-ICML-UNAM-740</th><td>TY: 187.5–(216)–237.5 × 2.5(3.4)–4.5; 1.3–(4)–6.3</td><td>21.3–(25.2)–27.5</td><td>30–(75.5)–90</td></tr><tr><td>ST: 207–(231)–270 × 5(5.5)–7</td><td></td><td></td></tr><tr><th>LEB-ICML-UNAM-797</th><td>TY: 180–(213)–240 × 2.5–(2.8)–3.8; 3–(3.5)–5</td><td>20–(21.5)–25</td><td>45–(65.5)–77.5</td></tr><tr><td>ST: 232.5–(248.3)–265 × 2–(4.2)–5.5</td><td></td><td></td></tr><tr><th>LEB-ICML-UNAM-850</th><td>TY: 180–(237.8)–257.5 × 2–(3.7)–4.5; 3–(4.8)–7.5</td><td>20–(22.5)–25</td><td>62–(71)–75</td></tr><tr><td>ST: 207.5–(251)–297.5 × 2.5–(3.8)–7.5</td><td></td><td></td></tr><tr><th><b><i>Celtodoryx ciocalyptoides</i> (</b>Burton, 1935<b>)</b> <b>for comparison</b></th></tr><tr><th><b>Lectotype</b> ZIN 10844e</th><td>SETYc: 170–(208)–290 × 1.5–(4.5)–6.5; 1.5–(5.7)–7.2</td><td>I: 48–(51)–56</td><td>62–(67)–72</td></tr><tr><td>AnSTd: 190–(273)–305 × 3.2–(8)–10.4</td><td>II: 22–(25)–30</td><td></td></tr><tr><th><b>Paratype</b> (MNHN D JV 93) of <i>Celtodoryx girardae</i> e</th><td>AnST: 165–(268)–320 × 5.8–(8.9)–12</td><td>I: 40–(48)–54</td><td>65–(74)–87</td></tr><tr><td>SETY:: 125–(195)–220 × 1.6–(4.2)–5.6, 2.4–(4.3)–6.4</td><td>II: 19–(23)–27</td><td></td></tr></tbody></table><p><sup>aTY</sup>,Smooth tylotes, <sup>bST</sup>, Smooth strongyles, <sup>cSETY</sup>,spined ends tylotes, <sup>dAnST</sup>,spined ends anisostrongyles, <sup>eSpicule</sup> measures from Henkel and Janussen 2011.</p>
Table 4 in Taxonomy and molecular phylogenetic position of new species and new records of Coelosphaeridae (Demospongiae: Poecilosclerida) from the Mexican Pacific
<p><b>Table 4.</b> Comparative data for the dimensions of the spicules (in µm) of <i>L. (L.) albemarlensis</i> and <i>L</i>. <i>(L.) isodictyalis</i>. Shass length × width; head diameter are given for megascleres and total length for arcuate isochelae and sigmas. Values in parentheses are means</p><table><tbody><tr><th><b><i>L. (L.) albemarlensis</i> material examined</b></th><th><b>Styles</b></th><th><b>Tylotes</b></th><th><b>Arcuate isochelae</b></th><th><b>Sigmas</b></th></tr></tbody><tbody><tr><th>AHF-1736-49</th><td>150–(161.5)–175 × 2.5–(3.4)–5</td><td>165–(175.1)–185 × 2.5–(2.5)–5; 4.5–(5.5)–7</td><td>17.5–(24.8)–30</td><td>15–(26.3)–37.5</td></tr><tr><th>AHF-608-36</th><td>160–(169.2)–180 × 2.5–(3.5)–5</td><td>180–(193.3)–205 × 2.5–(3.1)–5</td><td>17.5–(21.8)–27.5</td><td>15–(18.5)–25</td></tr><tr><th>LEB-ICML-UNAM-27</th><td>150–(169.5)–185 × 2.5–(4.5)–7.5</td><td>125–(178.6)–200 × 2.5–(3)–5; 3.8–(5)–6.3</td><td>11.3–(20.5)–32</td><td>15–(28.2)–40</td></tr><tr><th>LEB-ICML-UNAM-183</th><td>142.5–(159.5)–180 × 2.5–(4.2)–6.3</td><td>155–(170.3)–205 × 2.5–(4)–6.3; 5–(5.9)–7.5</td><td>20–(27)–30</td><td>20–(26.6)–31.3</td></tr><tr><th>LEB-ICML-UNAM-190</th><td>150–(166)–187.5 × 2.5–(4.9)–8.8</td><td>153.8–(172.5)–185 × 2.5–(3.6)–5; 3.8–(6)–8.8</td><td>12.5–(18.3)–27.5</td><td>17.5–(25.9)–30</td></tr><tr><th>LEB-ICML-UNAM-191</th><td>142.5–(172.2)–185 × 1.3–(5.2)–8.8</td><td>162–(178.8)–195 × 2.5–(3.5)–5; 5–(5.9)–7</td><td>12.5–(17.2)–27.5</td><td>15–(26)–31.3</td></tr><tr><th>LEB-ICML-UNAM-193</th><td>135–(157.5)–185 × 1.3–(4.3)–6.3</td><td>150–(174)–190 × 2.5–(3.9)–5; 5–(5.7)–6.3</td><td>22.5–(25.5)–30</td><td>20–(26.3)–35</td></tr><tr><th>LEB-ICML-UNAM-232</th><td>170–(183.4)–195 × 2.5–(5.9)–10</td><td>127.5–(172.8)–190 × 2.5–(3.6)–5</td><td>10–(19.4)–30</td><td>15–(25.1)–40</td></tr><tr><th>LEB-ICML-UNAM-720</th><td>165–(177.2)–190 × 2.5–(3.7)–5</td><td>170–(181.6)–200 × 2.5–(3.3)–5</td><td>12.5–(21.3)–27.5</td><td>15–(27.0)–40</td></tr><tr><th>LEB-ICML-UNAM-1018</th><td>145–(160.2)–175 × 2.5–(2.5)–2.5</td><td>180–(195.8)–215 × 2.5–(2.9)–5</td><td>22.5–(25.9)–30</td><td>15–(23.4)–27.5</td></tr><tr><th>LEB-ICML-UNAM-1104</th><td>150–(157.9)–175 × 2.5–(3.8)–5</td><td>175–(187.9)–215 × 2.5–(2.9)–5</td><td>17.5–(23.3)–27.5</td><td>20–(26.1)–30</td></tr><tr><th>LEB-ICML-UNAM-1369</th><td>150–(162.8)–180 × 2.5–(2.8)–5</td><td>170–(186.5)–200 × 2.5–(2.6)–5</td><td>20–(25.7)–30</td><td>20–(23.3)–27.5</td></tr><tr><th>LEB-ICML-UNAM-1443</th><td>145–(161.6)–175 × 2.5–(3.0)–5</td><td>170–(181.2)–195 × 2.5–(2.7)–5</td><td>20–(23.4)–30</td><td>20–(25.1)–32.5</td></tr><tr><th>LEB-ICML-UNAM-1553</th><td>150–(160.4)–180 × 2.5–(2.7)–5</td><td>170–(180.9)–195 × 2.5–(2.7)–5</td><td>15–(24.1)–30</td><td>17.5–(23.5)–27.5</td></tr><tr><th>LEB-ICML-UNAM-1579</th><td>155–(170.2)–190 × 2.5–(3.6)–5</td><td>180–(186.5)–195 × 2.5–(2.7)–5</td><td>12.5–(19.8)–27.5</td><td>15–(25.5)–37.5</td></tr><tr><th>LEB-ICML-UNAM-1581</th><td>150–(169.2)–185 × 2.5–(3.2)–5</td><td>170–(181.2)–200 × 2.5–(2.7)–5</td><td>12.5–(21.9)–27.5</td><td>17.5–(28.1)–40</td></tr><tr><th>LEB-ICML-UNAM-2374</th><td>125–(150.3)–175 × 2–(4.5)–7.5</td><td>162.5–(171.3)–190 × 3–(5)–6; 5–(5.7)–7.5</td><td>15–(25.5)–32</td><td>15–(26)–30</td></tr><tr><th>LEB-ICML-UNAM-2377</th><td>167.5–(185)–198 × 2.5–(5.7)–7.5</td><td>162.5–(190)–200 × 2.5–(4.2)–5; 5–(5.5)–6.3</td><td>12.5–(22.2)–31.3</td><td>17.5–(33.6)–40</td></tr><tr><th>LEB-ICML-UNAM-2379</th><td>142.5–(158)–165 × 1.3–(6.2)–7.5</td><td>120–(167)–182.5 × 2.5–(4.3)–5; 3.8–(4.8)–5.5</td><td>17.5–(25.3)–32.5</td><td>20–(26.5)–32.5</td></tr><tr><th>For comparison (non-examined material)</th></tr><tr><th><i>L</i>. (<i>L</i>.) <i>albemarlensis</i> from Desqueyroux-Faúndez and Van Soest 1997</th><td>123–(157)–190 × 4–8</td><td>107–(139)–170 × 5</td><td>16–26</td><td>16–26</td></tr><tr><th><i>L</i>. (<i>L</i>.) <i>isodictyalis</i> (Carter, 1882); from Rützler <i>et al.</i> 2007</th><td>148.6–(164.6)–175.2 × 3.8–(4.8)–5.7</td><td>177.9–(198.3)–207.9 × 3.1–(3.9)–4.2</td><td>19.6–(26.3)–41.4</td><td>18.3(21)–22.9</td></tr></tbody></table>
FIGURE 4 in Phylogenetic position and taxonomy of the enigmatic Orobanche krylowii (Orobanchaceae), a predominatly Asian species newly found in Albania (SE Europe)
FIGURE 4. Distribution of Orobanche krylowii based on the examined herbarium material and photos (big dots) as well as literature data (small dots). The locality in Albania is marked with a triangle.
FIGURE 1 in Phylogenetic position and taxonomy of the enigmatic Orobanche krylowii (Orobanchaceae), a predominatly Asian species newly found in Albania (SE Europe)
FIGURE 1. Maximum likelihood tree of nuclear ITS sequences of Orobanche, using the genus Diphelypaea as outgroup. Some clades with more sequences per species and/or several closely related species are collapsed to aid legibility. Orobanche krylowii is indicated in bold larger font. Numbers above branches are maximum likelihood, those below maximum parsimony bootstrap support values above 60%.
FIGURE 2 in Re-evaluation of the taxonomy of the Sri Lankan pigmy shrew Suncus fellowesgordoni (Soricidae: Crocidurinae) and its phylogenetic relationship with S. etruscus
FIGURE 2. Dorsal, lateral and ventral views of cranium; and lateral view of dentary, illustrating measurements taken in this study (see Materials and Methods for explanations of abbreviations).
FIGURE 5 in Re-evaluation of the taxonomy of the Sri Lankan pigmy shrew Suncus fellowesgordoni (Soricidae: Crocidurinae) and its phylogenetic relationship with S. etruscus
FIGURE 5. Ventral, dorsal and lateral views of the crania and mandibles of, A; Suncus fellowesgordoni (WHT 6818) and B; S. etruscus (WHT 6936). Arrows are pointing to the two denticulations of the incisor.
FIGURE 1 in Re-evaluation of the taxonomy of the Sri Lankan pigmy shrew Suncus fellowesgordoni (Soricidae: Crocidurinae) and its phylogenetic relationship with S. etruscus
FIGURE 1. Portraits of (A) Suncus fellowesgordoni from Agarapathana (WHT 6818, male, 47.7 mm HBL) and (B) S. etruscus from Anuradhapura (WHT 6936, male, 42.2 mm HBL).
FIGURE 3 in Re-evaluation of the taxonomy of the Sri Lankan pigmy shrew Suncus fellowesgordoni (Soricidae: Crocidurinae) and its phylogenetic relationship with S. etruscus
FIGURE 3. Phylogram inferred from Bayesian analysis of combined mitochondrial (cytochrome b + 16S) and nuclear (Rag 1) data under model GTR+I+G. Posterior probability and bootstrap values (expressed as percentages) are given above and below branches, respectively.
FIGURE 5 in Molecular phylogenetics and taxonomy of leaf-toed geckos (Phyllodactylidae: Phyllodactylus) inhabiting the peninsula of Baja California
FIGURE 5. Phylogenetic relationships of Mexican Phyllodactylus based on maximum parsimony (MP; A) and Bayesian inference (BI; B) of mitochondrial DNA (mtDNA). Numbers above nodes on MP tree represent nonparametric bootstrap proportions (BSP). Numbers above nodes on the Bayesian topology represent Bayesian posterior probabilities (BPP; * = 1.0). Gekko gecko was removed from the BI tree due to its long branch length. Refer to text for a description of loci and total base pairs (bp) sequenced.
FIGURE 2 in Molecular phylogenetics and taxonomy of leaf-toed geckos (Phyllodactylidae: Phyllodactylus) inhabiting the peninsula of Baja California
FIGURE 2. Phylogenetic relationships of Mexican Phyllodactylus based on a branch-and-bound maximum parsimony (MP) analysis of the concatenated dataset. Numbers above nodes represent MP bootstrap proportions (BSP) resulting from 10,000 pseudoreplicates.
FIGURE 3 in Molecular phylogenetics and taxonomy of leaf-toed geckos (Phyllodactylidae: Phyllodactylus) inhabiting the peninsula of Baja California
FIGURE 3. Phylogenetic relationships of Mexican Phyllodactylus based on Bayesian inference (BI) of the concatenated dataset. Numbers above and adjacent to nodes represent Bayesian posterior probabilities (BPP; * = 1.0) sampled from the posterior distribution of trees. Gekko gecko was removed from the tree due to its long branch length.
FIGURE 4 in Molecular phylogenetics and taxonomy of leaf-toed geckos (Phyllodactylidae: Phyllodactylus) inhabiting the peninsula of Baja California
FIGURE 4. Phylogenetic relationships of Mexican Phyllodactylus based on maximum parsimony (MP; A) and Bayesian inference (BI; B) of nuclear DNA (nDNA). Numbers above nodes on MP tree represent nonparametric bootstrap proportions (BSP). Numbers above nodes on the Bayesian topology represent Bayesian posterior probabilities (BPP; * = 1.0). Refer to text for a description of loci and total base pairs (bp) sequenced.
FIGURE 1 in Molecular phylogenetics and taxonomy of leaf-toed geckos (Phyllodactylidae: Phyllodactylus) inhabiting the peninsula of Baja California
FIGURE 1. Map of Baja California, the Gulf of California, southwestern USA, and northwestern Mexico illustrating the geographic location of samples of Phyllodactylus included in this study. Sample numbers correspond to those presented in Table 1. The break in geographic ranges in the Isthmus of La Paz region is due to unsuitable natural habitat (lack of rocky outcrops). Gray area represents the geographic range of P. nocticolus, black area represents the geographic range of P. xanti, striped area represents the range of P. unctus.
Figure 8 in Phylogenetic affinities and taxonomy of the Oligocene Diomedeoididae, and the basal divergences amongst extant procellariiform birds
Figure 8. Bones of extant procellariiform taxa to illustrate osteological features used in the phylogenetic analysis. A, B, ventral view of beak of A, Fulmarus glacialis (Procellariidae) and B, Bulweria bulwerii (Procellariidae); inset in A showing details of striae along inner margin of rhamphotheca. C, skull of Fregetta tropica (Oceanitinae). D, E, orbital region of D, Fr. tropica and E, Fu. glacialis. F, furcula of Oceanites oceanicus (Oceanitinae). G, H, os carpi ulnare of G, Pelagodroma marina (Oceanitinae) and H, Lugensa brevirostris (Procellariidae). I, J, humerus (caudal view) of I, L. brevirostris and J, Pe. marina. K–M, carpometacarpus of K, O. oceanicus, L, Puffinus huttoni (Procellariidae), and M, L. brevirostris. Abbreviations: afu, apophysis furculae; cbr, crus breve; ect, os ectethmoidale; fen, elongate fenestra delimited by dorsal margin of os lacrimale; fos, subovate fossa in rostral half of ventral surface of bill of Fulmarus, Macronectes, and Daption; fpn, second (dorsal) fossa pneumotricipitalis; lac, distal extension of os lacrimale; ldg, ledge on caudal humerus surface; orb, foramen orbitonasale; pis, processus pisiformis; prc, process formed by midsection of lateral margin of os ectethmoidale; str, striae along inner margin of rhamphotheca; tbd, tuberculum dorsale; tub, rostrodorsally directed tubular nostril of Fregetta tropica; unc, os uncinatum. Scale bars = 10 mm, except for G and H = 2 mm.
Figure 6 in Phylogenetic affinities and taxonomy of the Oligocene Diomedeoididae, and the basal divergences amongst extant procellariiform birds
Figure 6. Bones described by van Beneden (1871) in comparison to Rupelornis definitus specimens from the collection of IRSNB. A, 'Vanellus selysii' holotype (distal humerus, from van Beneden, 1871: fig. 2, reversed to facilitate comparison) in comparison to B, IRSNB Av 102a. C, incomplete humerus referred to 'Anas creccoides' (= Anas benedeni Sharpe, 1899) (from van Beneden, 1871: fig. 4) in comparison to D, IRSNB Av 111 (reversed to facilitate comparison). E, Rupelornis definitus holotype (distal tibiotarsus, from van Beneden, 1871: fig. 7) in comparison to F, IRSNB Av 103c. Scale bars = 10 mm and refer only to IRSNB fossils; bones from van Beneden (1871) are not to scale.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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