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Table 1 in Survey of gastrointestinal coccidian parasites of pet birds in Tehran
<p><b>Table 1.</b> The number and diversity of pet avian species investigated for digestive coccidian parasites in Tehran.</p><table><tbody><tr><th></th><th></th><th></th><th></th><th>Sample frequency</th><th>Infection</th></tr></tbody><tbody><tr><th>Order</th><td>Family</td><td>Common name</td><td>Scientific name</td><td>(%)</td><td>frequency</td></tr><tr><th>Psittaciformes</th><td>Psittaculidae</td><td>Budgerigar</td><td><i>Melopsittacus</i></td><td>15 (10.3)</td><td>−</td></tr><tr><th></th><td></td><td></td><td><i>undulatus</i></td><td></td><td></td></tr><tr><th></th><td></td><td>Lovebird</td><td><i>Agapornis</i> sp.</td><td>9 (6.2)</td><td>−</td></tr><tr><th></th><td></td><td>Ring necked</td><td><i>Psittacula krameri</i></td><td>3 (2.1)</td><td>−</td></tr><tr><th></th><td></td><td>parakeet</td><td></td><td></td><td></td></tr><tr><th></th><td></td><td>Eclectus parakeet</td><td><i>Eclectus roratus</i></td><td>2 (1.4)</td><td>−</td></tr><tr><th></th><td></td><td>Alexandrine parakeet</td><td><i>Psittacula eupatri</i></td><td>1 (0.7)</td><td>−</td></tr><tr><th></th><td></td><td>Lorikeet parakeet</td><td><i>Trichoglossus</i></td><td>1 (0.7)</td><td>−</td></tr><tr><th></th><td></td><td></td><td><i>moluccanus</i></td><td></td><td></td></tr><tr><th></th><td></td><td>African grey parrot</td><td><i>Psittacus erithacus</i></td><td>24 (16.5)</td><td>−</td></tr><tr><th></th><td>Psittacidae</td><td>Green cheeked</td><td><i>Pyrrhura molinae</i></td><td>3 (2.1)</td><td>−</td></tr><tr><th></th><td></td><td>parakeet</td><td></td><td></td><td></td></tr><tr><th></th><td></td><td>Conure</td><td><i>Aratinga solstitialis</i></td><td>1 (0.7)</td><td>−</td></tr><tr><th></th><td></td><td>Monk parakeet</td><td><i>Myiopsitta monachus</i></td><td>1 (0.7)</td><td>−</td></tr><tr><th></th><td></td><td>Ara</td><td><i>Ara</i> sp.</td><td>1 (0.7)</td><td>−</td></tr><tr><th></th><td>Cacatuidae</td><td>Cockatiel</td><td><i>Nymphicus</i></td><td>33 (22.8)</td><td>−</td></tr><tr><th></th><td></td><td></td><td><i>hollandicus</i></td><td></td><td></td></tr><tr><th></th><td></td><td>Cockatoo</td><td><i>Cacatua galerita</i></td><td>2 (1.4)</td><td>−</td></tr><tr><th>Passeriformes</th><td>Pycnonotidae</td><td>Bulbul</td><td><i>Pycnonotus leucotis</i></td><td>1 (0.7)</td><td>−</td></tr><tr><th></th><td>Fringillidae</td><td>Canary*</td><td><i>Serinus canaria</i></td><td>21 (14.5)</td><td>2</td></tr><tr><th></th><td></td><td>Finch</td><td><i>Taeniopygia guttata</i></td><td>7 (4.8)</td><td>−</td></tr><tr><th></th><td>Sturnidae</td><td>Mynah*</td><td><i>Acridotheres tristis</i></td><td>13 (9.0)</td><td>1</td></tr><tr><th>Columbiformes</th><td>Columbidae</td><td>Pigeon</td><td><i>Columba livia</i></td><td>6 (4.2)</td><td>−</td></tr><tr><th>Galliformes</th><td>Phasianidae</td><td>Quail*</td><td><i>Coturnix coturnix</i></td><td>1 (0.7)</td><td>1</td></tr><tr><th>Total</th><td></td><td></td><td></td><td>145</td><td>4</td></tr></tbody></table><p>*Species infected with parasites.</p>
TABLE 3. Distance matrix from nucleotide sequences for COI, 16 S in A new species of stauromedusa, Calvadosia festivala (Cnidaria: Staurozoa: Kishinouyeidae) from India
<p><b>TABLE 3.</b> Distance matrix from nucleotide sequences for COI, 16S, and 18S alignments from <i>Calvadosia</i> species closely related to <i>Calvadosia festivala</i> n. sp. “−”: represents absence of data for comparison (COI not available for <i>C. tasmaniensis</i> and <i>C. corbini</i>).</p><table><tbody><tr><th>Species</th><th>1</th><th>2</th><th>3</th><th>4</th><th>5</th></tr></tbody><tbody><tr><th>1. <i>C. tasmaniensis</i></th><td>COI: 0.0000 16S: 0.0000 18S: 0.0000</td><td></td><td></td><td></td><td></td></tr><tr><th>2. <i>C. lewisi</i></th><td>COI: − 16S: 0.0945 18S: 0.0017</td><td>COI: 0.0000 16S: 0.0000 18S: 0.0000</td><td></td><td></td><td></td></tr><tr><th>3. <i>C. corbini</i></th><td>COI: − 16S: 0.0985 18S: 0.0017</td><td>COI: − 16S: 0.1266 18S: 0.0038</td><td>COI: 0.0000 16S: 0.0000 18S: 0.0000</td><td></td><td></td></tr><tr><th>4. <i>C. festivala</i> n. sp.</th><td>COI: − 16S: 0.1400 18S: 0.0000</td><td>COI: 0.2215 16S: 0.1629 18S: 0.0014</td><td>COI: − 16S: 0.1430 18S: 0.0014</td><td>COI: 0.0000 16S: 0.0000 18S: 0.0000</td><td></td></tr><tr><th>5. <i>Calvadosia</i> sp. Moorea</th><td>COI: − 16S: 0.1917 18S: 0.0085</td><td>COI: 0.2506 16S: 0.2197 18S: 0.0070</td><td>COI: − 16S: 0.21009 18S: 0.0045</td><td>COI: 0.2158 16S: 0.2193 18S: 0.0083</td><td>COI: 0.0000 16S: 0.0000 18S: 0.0000</td></tr></tbody></table>
TABLE 2 in A new species of stauromedusa, Calvadosia festivala (Cnidaria: Staurozoa: Kishinouyeidae) from India
<p><b>TABLE 2.</b> Staurozoan species used in the phylogenetic analyses, including their respective GenBank accession numbers for each molecular marker. *Sequences from this study.</p><table><tbody><tr><th>Species</th><th>GenBank Accession Numbers</th><th></th></tr></tbody><tbody><tr><th></th><td>COI</td><td>16S</td><td>18S</td></tr><tr><th><i>Depastromorpha africana</i></th><td>KU257474.1</td><td>KU257499.1</td><td>KU308558.1</td></tr><tr><th><i>Haliclystus californiensis</i></th><td>GU201831.1</td><td>GU201829.1</td><td>KU308560.1</td></tr><tr><th><i>Manania gwilliami</i></th><td>KU257486.1</td><td>KU257512.1</td><td>KU308574.1</td></tr><tr><th><i>Calvadosia campanulata</i></th><td>KU257483.1</td><td>KU257508.1</td><td>KU308570.1</td></tr><tr><th><i>Calvadosia corbini</i></th><td>-</td><td>KU257502.1</td><td>KU308565.1</td></tr><tr><th><i>Calvadosia cruciformis</i></th><td>KU257487.1</td><td>KU257514.1</td><td>KU308576.1</td></tr><tr><th><i>Calvadosia cruxmelitensis</i></th><td>KU257484.1</td><td>KU257509.1</td><td>KU308571.1</td></tr><tr><th><i>Calvadosia festivala</i> n. sp. <i>*</i></th><td>PP715785*</td><td>PP711362*</td><td>PP711361*</td></tr><tr><th><i>Calvadosia lewisi</i></th><td>KU257492.1</td><td>KU257519.1</td><td>KU308581.1</td></tr><tr><th><i>Calvadosia nagatensis</i></th><td>OK356409.1</td><td>-</td><td>-</td></tr><tr><th><i>Calvadosia tasmaniensis</i></th><td>-</td><td>KU257510.1</td><td>KU308572.1</td></tr><tr><th><i>Calvadosia vanhoeffeni</i></th><td>KU257485.1</td><td>KU257511.1</td><td>KU308573.1</td></tr><tr><th><i>Calvadosia</i> sp. Moorea</th><td>KU257490.1</td><td>KU257517.1</td><td>KU308579.1</td></tr><tr><th><i>Calvadosia</i> sp. 1 New Zealand</th><td>KU257495.1</td><td>KU257521.1</td><td>KU308584.1</td></tr><tr><th><i>Calvadosia</i> sp. 2 New Zealand</th><td>KU257491.1</td><td>KU257518.1</td><td>KU308580.1</td></tr></tbody></table>
Table 1 in The complete mitochondrial genome of the leopard shark Triakis semifasciata (Triakidae)
<p><b>Table 1.</b> Mitochondrial genome of <i>Triakis semifasciata</i>: arrangement and annotation.</p><table><tbody><tr><th>Name</th><th>Type</th><th>Start</th><th>Stop</th><th>Strand</th><th>Length (bp)</th><th>Start</th><th>Stop</th><th>Anticodon</th><th>Continuity</th></tr></tbody><tbody><tr><th>trnF(gaa)</th><td></td><td>1</td><td>69</td><td>(+)</td><td>69</td><td></td><td></td><td></td><td>1</td></tr><tr><th>rrnS</th><td></td><td>71</td><td>1023</td><td>(+)</td><td>953</td><td></td><td></td><td></td><td>−3</td></tr><tr><th>trnV(tac)</th><td></td><td>1021</td><td>1092</td><td>(+)</td><td>72</td><td></td><td></td><td></td><td>23</td></tr><tr><th>rrnL</th><td></td><td>1116</td><td>2763</td><td>(+)</td><td>1648</td><td></td><td></td><td></td><td>−1</td></tr><tr><th>trnL2(taa)</th><td></td><td>2763</td><td>2837</td><td>(+)</td><td>75</td><td></td><td></td><td></td><td>0</td></tr><tr><th><i>nad1</i></th><td></td><td>2838</td><td>3812</td><td>(+)</td><td>975</td><td>ATG</td><td>TAA</td><td></td><td>0</td></tr><tr><th>trnl(gat)</th><td></td><td>3813</td><td>3882</td><td>(+)</td><td>70</td><td></td><td></td><td></td><td>1</td></tr><tr><th>trnQ(ttg)</th><td></td><td>3884</td><td>3955</td><td>(-)</td><td>72</td><td></td><td></td><td></td><td>0</td></tr><tr><th>trnM(cat)</th><td></td><td>3956</td><td>4024</td><td>(+)</td><td>69</td><td></td><td></td><td></td><td>0</td></tr><tr><th><i>nad2</i></th><td></td><td>4025</td><td>5071</td><td>(+)</td><td>1047</td><td>ATG</td><td>TAG</td><td></td><td>−2</td></tr><tr><th>trnW(tca)</th><td></td><td>5070</td><td>5140</td><td>(+)</td><td>71</td><td></td><td></td><td></td><td>1</td></tr><tr><th>trnN(tgc)</th><td></td><td>5142</td><td>5210</td><td>(-)</td><td>69</td><td></td><td></td><td></td><td>0</td></tr><tr><th>trnN(gtt)</th><td></td><td>5211</td><td>5283</td><td>(-)</td><td>73</td><td></td><td></td><td></td><td>6</td></tr><tr><th>OL</th><td></td><td>5290</td><td>5319</td><td>(+)</td><td>30</td><td></td><td></td><td></td><td>1</td></tr><tr><th>trnC(gca)</th><td></td><td>5321</td><td>5389</td><td>(-)</td><td>69</td><td></td><td></td><td></td><td>1</td></tr><tr><th>trnY(gta)</th><td></td><td>5391</td><td>5460</td><td>(-)</td><td>70</td><td></td><td></td><td></td><td>1</td></tr><tr><th><i>cox1</i></th><td></td><td>5462</td><td>7018</td><td>(+)</td><td>1557</td><td>GTG</td><td>TAA</td><td></td><td>0</td></tr><tr><th>trnS2(tga)</th><td></td><td>7019</td><td>7089</td><td>(-)</td><td>71</td><td></td><td></td><td></td><td>3</td></tr><tr><th>trnD(gtc)</th><td></td><td>7093</td><td>7162</td><td>(+)</td><td>70</td><td></td><td></td><td></td><td>7</td></tr><tr><th><i>cox2</i></th><td></td><td>7170</td><td>7860</td><td>(+)</td><td>691</td><td>ATG</td><td>T(AA)</td><td></td><td>0</td></tr><tr><th>trnK(ttt)</th><td></td><td>7861</td><td>7934</td><td>(+)</td><td>74</td><td></td><td></td><td></td><td>1</td></tr><tr><th><i>atp8</i></th><td></td><td>7936</td><td>8103</td><td>(+)</td><td>168</td><td>ATG</td><td>TAA</td><td></td><td>−10</td></tr><tr><th><i>atp6</i></th><td></td><td>8094</td><td>8777</td><td>(+)</td><td>684</td><td>ATG</td><td>TAA</td><td></td><td>−1</td></tr><tr><th>cox3</th><td></td><td>8777</td><td>9562</td><td>(+)</td><td>786</td><td>ATG</td><td>TAA</td><td></td><td>2</td></tr><tr><th>trnG(tcc)</th><td></td><td>9565</td><td>9634</td><td>(+)</td><td>70</td><td></td><td></td><td></td><td>0</td></tr><tr><th><i>nad3</i></th><td></td><td>9635</td><td>9985</td><td>(+)</td><td>351</td><td>ATG</td><td>TAG</td><td></td><td>−2</td></tr><tr><th>trnR(tcg)</th><td></td><td>9984</td><td>10,053</td><td>(+)</td><td>70</td><td></td><td></td><td></td><td>0</td></tr><tr><th><i>nad4l</i></th><td></td><td>10,054</td><td>10,350</td><td>(+)</td><td>297</td><td>ATG</td><td>TAA</td><td></td><td>−7</td></tr><tr><th><i>nad4</i></th><td></td><td>10,344</td><td>11,724</td><td>(+)</td><td>1381</td><td>ATG</td><td>T(AA)</td><td></td><td>0</td></tr><tr><th>trnH(gtg)</th><td></td><td>11,725</td><td>11,793</td><td>(+)</td><td>69</td><td></td><td></td><td></td><td>0</td></tr><tr><th>trnS1(gct)</th><td></td><td>11,794</td><td>11,860</td><td>(+)</td><td>67</td><td></td><td></td><td></td><td>0</td></tr><tr><th>trnL1(tag)</th><td></td><td>11,861</td><td>11,932</td><td>(+)</td><td>72</td><td></td><td></td><td></td><td>0</td></tr><tr><th><i>nad5</i></th><td></td><td>11,933</td><td>13,762</td><td>(+)</td><td>1830</td><td>ATG</td><td>TAA</td><td></td><td>−5</td></tr><tr><th><i>nad6</i></th><td></td><td>13,758</td><td>14,279</td><td>(-)</td><td>522</td><td>ATG</td><td>AGG</td><td></td><td>0</td></tr><tr><th>trnE(ttc)</th><td></td><td>14,280</td><td>14,349</td><td>(-)</td><td>70</td><td></td><td></td><td></td><td>2</td></tr><tr><th><i>cob</i></th><td></td><td>14,352</td><td>15,497</td><td>(+)</td><td>1146</td><td>ATG</td><td>TAG</td><td></td><td>−1</td></tr><tr><th>trnT(tgt)</th><td></td><td>15,497</td><td>15,568</td><td>(+)</td><td>72</td><td></td><td></td><td></td><td>2</td></tr><tr><th>trnP(tgg)</th><td></td><td>15,571</td><td>15,639</td><td>(-)</td><td>69</td><td></td><td></td><td></td><td>278</td></tr><tr><th>CR</th><td></td><td>15,640</td><td>16,613</td><td></td><td>974</td><td></td><td></td><td></td><td></td></tr><tr><th>OH</th><td></td><td>15,918</td><td>16,612</td><td>(+)</td><td>695</td><td></td><td></td><td></td><td></td></tr></tbody></table>
Table 1 in The mitochondrial genome of the Yellowtail Snapper Ocyurus chrysurus (Bloch, 1791) (Perciformes: Lutjanidae)
<p><b>Table 1.</b> Mitochondrial genome of <i>Ocyurus chrysurus</i>. Arrangement and annotation.</p><table><tbody><tr><th>Name</th><th>Type</th><th>Start</th><th>Stop</th><th>Strand</th><th>Length (bp)</th><th>Start</th><th>Stop</th><th>Anticodon</th><th>Continuity</th></tr></tbody><tbody><tr><th>trnF</th><td>tRNA</td><td>1</td><td>68</td><td>+</td><td>68</td><td></td><td></td><td>GAA</td><td>0</td></tr><tr><th>rrnS</th><td>rRNA</td><td>69</td><td>1020</td><td>+</td><td>952</td><td></td><td></td><td></td><td>0</td></tr><tr><th>trnV</th><td>tRNA</td><td>1021</td><td>1092</td><td>+</td><td>72</td><td></td><td></td><td>TAC</td><td>46</td></tr><tr><th>rrnL</th><td>rRNA</td><td>1139</td><td>2790</td><td>+</td><td>1652</td><td></td><td></td><td></td><td>0</td></tr><tr><th>trnL2</th><td>tRNA</td><td>2791</td><td>2864</td><td>+</td><td>74</td><td></td><td></td><td>TAA</td><td>0</td></tr><tr><th><i>nad1</i></th><td>PCG</td><td>2865</td><td>3839</td><td>+</td><td>975</td><td>ATG</td><td>TAA</td><td></td><td>3</td></tr><tr><th>trnI</th><td>tRNA</td><td>3843</td><td>3912</td><td>+</td><td>70</td><td></td><td></td><td>GAT</td><td>−1</td></tr><tr><th>trnQ</th><td>tRNA</td><td>3912</td><td>3982</td><td>−</td><td>71</td><td></td><td></td><td>TTG</td><td>−1</td></tr><tr><th>trnM</th><td>tRNA</td><td>3982</td><td>4050</td><td>+</td><td>69</td><td></td><td></td><td>CAT</td><td>0</td></tr><tr><th><i>nad2</i></th><td>PCG</td><td>4051</td><td>5097</td><td>+</td><td>1047</td><td>ATG</td><td>TAA</td><td></td><td>−1</td></tr><tr><th>trnW</th><td>tRNA</td><td>5097</td><td>5168</td><td>+</td><td>72</td><td></td><td></td><td>TCA</td><td>0</td></tr><tr><th>trnA</th><td>tRNA</td><td>5169</td><td>5237</td><td>−</td><td>69</td><td></td><td></td><td>TGC</td><td>1</td></tr><tr><th>trnN</th><td>tRNA</td><td>5239</td><td>5311</td><td>−</td><td>73</td><td></td><td></td><td>GTT</td><td>2</td></tr><tr><th>OL</th><td>PCG</td><td>5314</td><td>5352</td><td>+</td><td>39</td><td></td><td></td><td></td><td>−2</td></tr><tr><th>trnC</th><td>tRNA</td><td>5351</td><td>5417</td><td>−</td><td>67</td><td></td><td></td><td>GCA</td><td>0</td></tr><tr><th>trnY</th><td>tRNA</td><td>5418</td><td>5487</td><td>−</td><td>70</td><td></td><td></td><td>GTA</td><td>1</td></tr><tr><th><i>cox1</i></th><td>PCG</td><td>5489</td><td>7039</td><td>+</td><td>1551</td><td>GTG</td><td>TAA</td><td></td><td>2</td></tr><tr><th>trnS2</th><td>tRNA</td><td>7042</td><td>7112</td><td>−</td><td>71</td><td></td><td></td><td>TGA</td><td>3</td></tr><tr><th>trnD</th><td>tRNA</td><td>7116</td><td>7187</td><td>+</td><td>72</td><td></td><td></td><td>GTC</td><td>6</td></tr><tr><th><i>cox2</i></th><td>PCG</td><td>7194</td><td>7886</td><td>+</td><td>693</td><td>ATG</td><td>TAG</td><td></td><td>−2</td></tr><tr><th>trnK</th><td>tRNA</td><td>7885</td><td>7959</td><td>+</td><td>75</td><td></td><td></td><td>TTT</td><td>1</td></tr><tr><th><i>atp8</i></th><td>PCG</td><td>7961</td><td>8128</td><td>+</td><td>168</td><td>ATG</td><td>TAA</td><td></td><td>−10</td></tr><tr><th><i>atp6</i></th><td>PCG</td><td>8119</td><td>8802</td><td>+</td><td>684</td><td>ATG</td><td>TAA</td><td></td><td>−1</td></tr><tr><th><i>cox3</i></th><td>PCG</td><td>8802</td><td>9587</td><td>+</td><td>786</td><td>ATG</td><td>TAA</td><td></td><td>−1</td></tr><tr><th>trnG</th><td>tRNA</td><td>9587</td><td>9658</td><td>+</td><td>72</td><td></td><td></td><td>TCC</td><td>0</td></tr><tr><th><i>nad3</i></th><td>PCG</td><td>9659</td><td>10,009</td><td>+</td><td>351</td><td>ATG</td><td>TAG</td><td></td><td>−2</td></tr><tr><th>trnR</th><td>tRNA</td><td>10,008</td><td>10,076</td><td>+</td><td>69</td><td></td><td></td><td>TCG</td><td>0</td></tr><tr><th><i>nad4l</i></th><td>PCG</td><td>10,077</td><td>10,373</td><td>+</td><td>297</td><td>ATG</td><td>TAA</td><td></td><td>−7</td></tr><tr><th><i>nad4</i></th><td>PCG</td><td>10,367</td><td>11,747</td><td>+</td><td>1381</td><td>ATG</td><td>T</td><td></td><td>0</td></tr><tr><th>trnH</th><td>tRNA</td><td>11,748</td><td>11,816</td><td>+</td><td>69</td><td></td><td></td><td>GTG</td><td>0</td></tr><tr><th>trnS1</th><td>tRNA</td><td>11,817</td><td>11,884</td><td>+</td><td>68</td><td></td><td></td><td>GCT</td><td>4</td></tr><tr><th>trnL1</th><td>tRNA</td><td>11,889</td><td>11,961</td><td>+</td><td>73</td><td></td><td></td><td>TAG</td><td>0</td></tr><tr><th><i>nad5</i></th><td>PCG</td><td>11,962</td><td>13,800</td><td>+</td><td>1839</td><td>ATG</td><td>TAA</td><td></td><td>−4</td></tr><tr><th><i>nad6</i></th><td>PCG</td><td>13,797</td><td>14,318</td><td>−</td><td>522</td><td>ATG</td><td>TAG</td><td></td><td>0</td></tr><tr><th>trnE</th><td>tRNA</td><td>14,319</td><td>14,387</td><td>−</td><td>69</td><td></td><td></td><td>TTC</td><td>6</td></tr><tr><th><i>Cob</i></th><td>PCG</td><td>14,394</td><td>15,534</td><td>+</td><td>1141</td><td>ATG</td><td>T</td><td></td><td>0</td></tr><tr><th>trnT</th><td>tRNA</td><td>15,535</td><td>15,606</td><td>+</td><td>72</td><td></td><td></td><td>TGT</td><td>−1</td></tr><tr><th>trnP</th><td>tRNA</td><td>15,606</td><td>15,675</td><td>−</td><td>70</td><td></td><td></td><td>TGG</td><td>254</td></tr><tr><th>CR</th><td></td><td>15,675</td><td>16,502</td><td>+</td><td>827</td><td></td><td></td><td></td><td>51</td></tr></tbody></table>
Table 1 in Nesting behaviour of Neotropical social wasps of the genus Clypearia de Saussure (Hymenoptera: Vespidae: Polistinae)
<p><b>Table 1.</b> Nests of the social wasp <i>Clypearia</i> (Hymenoptera: Vespidae) fixed in plant substrate in ecological conditions in Cerrado and Atlantic Forest of Minas Gerais State, and associated with ants in Amazon Forest, Amazonas, and Pará State, Brazil.</p><table><tbody><tr><th>Species</th><th>Substrate, ecological condition and state</th></tr></tbody><tbody><tr><th><i>C. angustior</i></th><td>Trunk of arboreous species, around 80 m from the water and 5 m above the ground, Barroso</td></tr><tr><th></th><td>municipality, Minas Gerais State.</td></tr><tr><th><i>C. angustior</i></th><td>Trunk of <i>Pyrus</i> sp. (Rosaceae) in an agricultural area, around 5 m from a river and 1.5 m above the</td></tr><tr><th></th><td>ground (Barroso, Minas Gerais State, Brazil).</td></tr><tr><th><i>C. angustior</i></th><td>Tree trunk in an ombrophilous forest, around 3 m from a river and 3.2 m above the ground (Parque</td></tr><tr><th></th><td>Estadual do Rio Doce, Minas Gerais State, Brazil).</td></tr><tr><th><i>C. apicipennis</i></th><td>Tree trunk in a wetland (Manaus, Amazonas State, Brazil) in the Amazon rainforest.</td></tr><tr><th><i>C. weyrauchi</i></th><td>Two colonies in mango tree <i>Mangifera indica</i> L. (Anacardiaceae), over 4 m above the ground, in</td></tr><tr><th></th><td>Amazonas State.</td></tr><tr><th><i>C. sulcata</i></th><td>In a non-identified tree, over 1.5 m above the ground, 7 m from a lake and 10 cm and 40 cm,</td></tr><tr><th></th><td>respectively, from two colonies of the ant <i>Azteca chartifex</i>, Pará State.</td></tr></tbody></table>
Table 3 in Variable foraging and flower probing behaviour of sunbird pollinators of the South African Pelargonium fulgidum
<p><b>Table 3.</b> Summary of sunbird foraging behaviour. During consistent bouts none of the aspects of foraging behaviour quantified here changed during a plant visit, whereas during variable bouts foraging behaviour and/or flower probing direction changed during a plant visit. Values represent total number of foraging bouts (2022/2023 bouts).</p><table><tbody><tr><th></th><th></th><th></th><th></th><th></th><th></th><th>Nototrobic and</th></tr></tbody><tbody><tr><th></th><td></td><td>Nototribic flower</td><td>Sternotribic flower</td><td>sternotrobic</td></tr><tr><th></th><td></td><td>probing</td><td>probing</td><td>flower probing</td></tr><tr><th></th><td></td><td>Female</td><td>Male</td><td>Female</td><td>Male</td><td>Female</td><td>Male</td></tr><tr><th>Consistent</th><td>Hovering</td><td>0</td><td>0</td><td>9 (0/9)</td><td>10 (0/10)</td><td></td><td></td></tr><tr><th></th><td>Alternative perch</td><td>4 (3/1)</td><td>9 (2/7)</td><td>15 (6/9)</td><td>10 (2/8)</td><td></td><td></td></tr><tr><th></th><td>Inflorescence perch</td><td>23 (3/20)</td><td>10 (3/7)</td><td>2 (0/2)</td><td>2 (1/1)</td><td></td><td></td></tr><tr><th>Variable</th><td>Inflorescence perch</td><td></td><td></td><td></td><td></td><td>2 (0/2)</td><td></td></tr><tr><th></th><td>Hovering and alternative perch</td><td></td><td></td><td>1 (0/1)</td><td></td><td></td><td></td></tr><tr><th></th><td>Hovering and inflorescence perch</td><td></td><td></td><td></td><td></td><td>1 (0/1)</td><td></td></tr><tr><th></th><td>Alternative perch and inflorescence perch</td><td></td><td></td><td></td><td>1 (0/1)</td><td>1 (0/1)</td><td></td></tr></tbody></table>
TABLE 1 in Hysterium madraspatanum (Hysteriaceae), a new species from Tropical Dry Evergreen Forest of Tamil Nadu, India
<p><b>TABLE 1.</b> Taxa names, Culture accession, and corresponding GenBank accession numbers of the taxa used in the phylogenetic analyses. Newly generated sequences in this study are indicated in bold.</p><table><tbody><tr><th><b>Taxon</b></th><th><b>Culture accession</b></th><th><b>GenBank accession Number</b></th></tr></tbody><tbody><tr><th><i>Gloniopsis leucaenae</i></th><td>MFLUCC17-2425</td><td>NR163334</td></tr><tr><th><i>Gloniopsis calami</i></th><td>MFLUCC14-0049</td><td>MN860550</td></tr><tr><th><i>Hysterobrevium constrictum</i></th><td>JCM2753</td><td>LC228641</td></tr><tr><th><i>Hysterobrevium mori</i></th><td>-</td><td>KY496739.1</td></tr><tr><th><i>Rhytidhysteron thailandicum</i></th><td>MFLU:19-2373</td><td>MN989428</td></tr><tr><th><i>Rhytidhysteron mangrovei</i></th><td>MFLU 18-1894</td><td>NR165548.1</td></tr><tr><th><i>Rhytidhysteron chromolaenae</i></th><td>MFLUCC17-1516</td><td>NR171860</td></tr><tr><th><i>Rhytidhysteron subrufulum</i></th><td>SDBR-CMU475</td><td>OQ943972</td></tr><tr><th><i>Rhytidhysteron magnoliae</i></th><td>KUMCC21-0478</td><td>OP494093</td></tr><tr><th><i>Rhytidhysteron neorufulum</i></th><td>MFLUCC13-0221</td><td>KU377562</td></tr><tr><th><i>Hysterium rhizophorae</i></th><td>PUFD43</td><td>MG844284.1</td></tr><tr><th><i>Hysterium pulicare</i></th><td>CBS240.34</td><td>MH855497</td></tr><tr><th><i>Hysterium angustatum</i></th><td>MFLUCC:11-0004</td><td>MN608547</td></tr><tr><th><i>Hysterium angustatum</i></th><td>GZCC 19-0119</td><td>OR225030.1</td></tr><tr><th><i>Hysterium madraspatanum</i></th><td><b>MRL-MCC001</b></td><td><b>OR420067</b></td></tr><tr><th><i>Anteaglonium rubescens</i></th><td>CBS 143911</td><td>NR164489.1</td></tr><tr><th><i>Anteaglonium parvulum</i></th><td>17626ITS</td><td>MN582759</td></tr><tr><th><i>Anteaglonium gordoniae</i></th><td>C332</td><td>MK347761</td></tr><tr><th><i>Anteaglonium hydei</i></th><td>GZCC 20-0196</td><td>OR224994.1</td></tr><tr><th><i>Anteaglonium lusitanicum</i></th><td>AMI-SPL647</td><td>OP441407</td></tr></tbody></table>
TABLE 1 in Description and natural history notes of the tadpole of Proceratophrys belzebul (Anura: Odontophrynidae)
<p><b>TABLE 1.</b> Morphological measurements (mm) of 12 tadpoles of <i>Proceratophrys belzebul:</i> total length (TL), body length (BL), maximum body width (BW), body height (BH), tail length (TAL), maximum tail height (MTH), tail muscle width at the same level (TMW), tail muscle height at body-tail junction (TMH), upper fin height (UFH), lower fin height (LFH), eye diameter (ED), interorbital distance (IOD), internarial distance (IND), distance from center of naris to center of eye (NE), nostril-snout distance (NSD), eye-snout distance (ES). Values presented as mean ± standard deviation (range).</p><table><tbody><tr><th><b>Character</b></th><th><b>Stage 35 (n = 3)</b></th><th><b>Stage 37 (n = 1)</b></th><th><b>Stage 39 (n = 3)</b></th><th><b>Stage 41 (n = 5)</b></th></tr></tbody><tbody><tr><th>TL</th><td>28.8 ± 1.44 (26.8–29.6)</td><td>34.6</td><td>31.2 ± 0.61 (30.8–32)</td><td>30.7 ± 5.58 (20.3–34.3)</td></tr><tr><th>BL</th><td>12.9 ± 0.75 (12.1–13.6)</td><td>14.2</td><td>13.4 ± 0.42 (12.8–13.6)</td><td>12.7 ± 1.11 (10.6–13.5)</td></tr><tr><th>BW</th><td>9.5 ± 0.44 (8.8–9.6)</td><td>9.1</td><td>9.9 ± 0.61 (9.1–10.3)</td><td>10.6 ± 1.07 (8.6–10.9)</td></tr><tr><th>BH</th><td>5.6 ± 0.36 (5.1–5.8)</td><td>5.9</td><td>5.8 ± 0.17 (5.8–6.1)</td><td>5.9 ± 0.66 (4.6–6)</td></tr><tr><th>TAL</th><td>16.2 ± 0.50 (15.7–16.7)</td><td>20.8</td><td>18.4 ± 0.55 (17.8–18.9)</td><td>18.4 ± 4.95 (8.9–21.9)</td></tr><tr><th>MTH</th><td>6.5 ± 0.4 (6–6.8)</td><td>6.6</td><td>6.8 ± 0.49 (6–6.9)</td><td>6.9 ± 0.59 (5.6–7)</td></tr><tr><th>TMW</th><td>3.1 ± 0.15 (3- 3.3)</td><td>2.8</td><td>3.3 ± 0.40 (2.8–3.6)</td><td>3.1 ± 0.17 (2.9–3.3)</td></tr><tr><th>TMH</th><td>3.3 ± 0.23 (2.9–3.3)</td><td>3.3</td><td>3.5 ± 0.26 (3.4–3.9)</td><td>3.6 ± 0.34 (3.1–4)</td></tr><tr><th>UFH</th><td>2.4 ± 0.42 (1.8–2.6)</td><td>2.2</td><td>2.3 ± 0.29 (2.3–2.8)</td><td>2.1 ± 0.36 (1.6–2.6)</td></tr><tr><th>LFH</th><td>1.8 ± 0.17 (1.5–1.8)</td><td>1.6</td><td>2 ± 0.46 (1.4–2.3)</td><td>1.8 ± 0.18 (1.4–1.8)</td></tr><tr><th>ED</th><td>1.5 ± 0.20 (1.3–1.7)</td><td>1.8</td><td>1.8 ± 0.12 (1.6–1.8)</td><td>1.6 ± 0.11 (1.6–1.8)</td></tr><tr><th>IOD</th><td>3.9 ± 0.32 (3.4–4)</td><td>3.8</td><td>4.3 ± 0.10 (4.2–4.4)</td><td>4.3 ± 0.11 (4.1–4.4)</td></tr><tr><th>IND</th><td>2.1 ± 0 (2.1–2.1)</td><td>2.2</td><td>2.1 ± 0.15 (1.9–2.2)</td><td>2 ± 0.23 (1.6–2.2)</td></tr><tr><th>NE</th><td>1.8 ± 0.06 (1.7–1.8)</td><td>2</td><td>2.1 ± 0.06 (2–2.1)</td><td>2.1 ± 0.05 (2-2.1)</td></tr><tr><th>NSD</th><td>1.5 ± 0.26 (1.1–1.6)</td><td>1.4</td><td>1.3 ± 0 (1.3–1.3)</td><td>1.4 ± 0.13 (1.1–1.4)</td></tr><tr><th>ES</th><td>3 ± 0.35 (2.6–3.3)</td><td>2.9</td><td>2.9 ± 0.10 (2.8–3)</td><td>2.9 ± 0.18 (2.6–3.1)</td></tr></tbody></table>
Table 2 in Correction to: First description of ECHinoCoCCUS oRtleppi infection in China
<p><b>Table 2</b> Summary of animal infection of Echinococcus ortleppi</p><table><tbody><tr><th>Year</th><th>Country</th><th>Species</th><th>No. infected</th><th>Reference</th></tr><tr><th>Asia</th></tr></tbody><tbody><tr><th>2009</th><td>India</td><td>Cattle/buffalo/pig</td><td>3/2/4</td><td>Pednekar et al. [8]</td></tr><tr><th>2009</th><td>Vietnam</td><td>Monkey</td><td>1</td><td>Pednekar et al. [8]</td></tr><tr><th>2015</th><td>Egypt</td><td>Camel</td><td>1</td><td>Amer et al. [11]</td></tr><tr><th>2016</th><td>Bhutan</td><td>Cattle</td><td>1</td><td>Thapa et al. [33]</td></tr><tr><th>2017</th><td>Iran</td><td>Camel</td><td>1</td><td>Ebrahimipour et al. [34]</td></tr><tr><th>Africa</th></tr><tr><th>2004</th><td>Kenya</td><td>Cattle/pig</td><td>2/1</td><td>Dinkel et al. [9]</td></tr><tr><th>2010–2012</th><td>South Africa</td><td>Cow</td><td>1</td><td>Mogoye et al. [27]</td></tr><tr><th>2013</th><td>Sudan</td><td>Camel</td><td>1</td><td>Ahmed et al. [35]</td></tr><tr><th>2013</th><td>Kenya</td><td>Cattle/goat/sheep</td><td>23/3/2</td><td>Mbaya et al. [10]</td></tr><tr><th>2015</th><td>Ethiopia</td><td>Cattle/pig</td><td>5/1</td><td>Tigre et al. [36]</td></tr><tr><th>2016</th><td>Kenya</td><td>Cattle/goat/camel/sheep</td><td>54/3/2/1</td><td>Addy et al. [3]</td></tr><tr><th>2016</th><td>Zambia</td><td>Cattle/pig</td><td>52/1</td><td>Addy et al. [3]</td></tr><tr><th>2016</th><td>Namibia</td><td>Cattle/oryx</td><td>35/3</td><td>Addy et al. [3]</td></tr><tr><th>2016</th><td>Ethiopia</td><td>Cattle</td><td>7</td><td>Addy et al. [3]</td></tr><tr><th>2016</th><td>Sudan</td><td>Cattle/camel</td><td>15/1</td><td>Addy et al. [3]</td></tr><tr><th>2018</th><td>Kenya</td><td>Dog</td><td>1</td><td>Mulinge et al. [37]</td></tr><tr><th>America</th></tr><tr><th>2002</th><td>Argentina</td><td>Cattle/dog</td><td>5/2</td><td>Kamenetzky et al. [25]</td></tr><tr><th>2012</th><td>Brazil</td><td>Cattle</td><td>277</td><td>Balbinotti et al. [38]</td></tr><tr><th>2016</th><td>Brazil</td><td>Cattle</td><td>7</td><td>Addy et al. [3]</td></tr><tr><th>2016</th><td>Brazil</td><td>Bovine</td><td>250</td><td>Monteiro et al. [39]</td></tr><tr><th>2018</th><td>Chile</td><td>Cattle</td><td>2</td><td>Correa et al. [41]</td></tr><tr><th>Europe</th></tr><tr><th>2012</th><td>UK</td><td>Spotted deer</td><td>1</td><td>Boufana et al. [12]</td></tr><tr><th>2014</th><td>France</td><td>Cattle</td><td>7</td><td>Grenouillet et al. [29]</td></tr><tr><th>2016</th><td>France</td><td>Cattle</td><td>7</td><td>Addy et al. [3]</td></tr><tr><th>2018</th><td>Bosnia and Herzegovina</td><td>Crested porcupine</td><td>1</td><td>Hodzic et al. [40]</td></tr><tr><th>2008</th><td>Italy</td><td>Cattle</td><td>1</td><td>Casulli et al. [42]</td></tr></tbody></table>
TABLE 2. The closest hits using a in Myxotrichum persicum sp. nov., and two new combinations in the genus Myxotrichum
<p><b>TABLE 2</b>. The closest hits using a MegaBLAST search of the LSU, ITS, <i>MCM7</i> and <i>RPB1</i> sequences of Malbranchea <i>circinata</i> and <i>M. flavorosea</i>.</p><table><tbody><tr><th><b>Species</b></th><th><b>Sequence</b></th><th><b>Blast hits</b></th><th><b>Query</b></th><th><b>Identity</b></th><th><b>Gaps</b></th></tr></tbody><tbody><tr><th><i>Malbranchea circinata</i></th><td>LSU</td><td><i>Myxotrichum setosum</i> (CBS:260.52, GenBank MH868555)</td><td>66%</td><td>98% (854/871)</td><td>0% (0/871)</td></tr><tr><td>ITS</td><td><i>Myxotrichum chartarum</i> (NBRC 31717, GenBank LC639295)</td><td>99%</td><td>94% (874/925)</td><td>0% (8/925)</td></tr><tr><td><i>MCM7</i></td><td><i>Myxotrichum chartarum</i> (NBRC 31717, GenBank LC639235)</td><td>99%</td><td>91% (542/598)</td><td>0% (1/598)</td></tr><tr><td><i>RPB1</i></td><td><i>Myxotrichum chartarum</i> (NBRC 31717, GenBank LC639271)</td><td>99%</td><td>88% (597/676</td><td>0% (0/676)</td></tr><tr><th><i>Malbranchea flavorosea</i></th><td>LSU</td><td><i>Myxotrichum setosum</i> (CBS:260.52, GenBank MH868555)</td><td>100%</td><td>99 % (611/615)</td><td>0% (1/615)</td></tr><tr><td>ITS</td><td><i>Myxotrichum stipitatum</i> (CBS:393.62, GenBank MH858191)</td><td>88%</td><td>98 % (506/518)</td><td>0% (2/518)</td></tr><tr><td><i>MCM7</i></td><td><i>Myxotrichum stipitatum</i> (NBRC 31721, GenBank LC639236)</td><td>100%</td><td>98 % (587/597)</td><td>0% (0/597)</td></tr><tr><td><i>RPB1</i></td><td><i>Myxotrichum stipitatum</i> (NBRC 31721, GenBank LC639272)</td><td>99%</td><td>98 % (691/703)</td><td>0% (0/703)</td></tr></tbody></table>
Table 2 in Variable foraging and flower probing behaviour of sunbird pollinators of the South African Pelargonium fulgidum
<p><b>Table 2.</b> Mean ± standard deviation (SD) (sample size) of sunbird measurements.</p><table><tbody><tr><th></th><th><i>Cinnyris chalybeus</i></th></tr></tbody><tbody><tr><th></th><td>Male</td><td>Female</td></tr><tr><th>Bill length (mm)**</th><td>18.59 ± 1.03 (21)</td><td>16.45 ± 0.73 (6)</td></tr><tr><th>Bill base diameter (mm)</th><td>2.88 ± 0.27 (20)</td><td>2.92 ± 0.23 (6)</td></tr><tr><th>Bill height (mm)</th><td>3.53 ± 0.40 (21)</td><td>3.30 ± 0.44 (6)</td></tr></tbody></table><p>**Differed significantly between male and female sunbirds (P <0.05).</p>
Table 1 in Variable foraging and flower probing behaviour of sunbird pollinators of the South African Pelargonium fulgidum
<p><b>Table 1.</b> Mean ± standard deviation (SD) (sample size) of Pelargonium <i>fulgidum</i> measurements.</p><table><tbody><tr><th></th><th>P. fulgidum</th></tr></tbody><tbody><tr><th>Peduncle length (mm)</th><td>45.5 ± 12.3 (35)</td></tr><tr><th>Peduncle angle (°)</th><td>24.2 ± 15.1 (35)</td></tr><tr><th>Pedicel length (mm)</th><td>32.4 ± 3.2 (35)</td></tr><tr><th>Number of open flowers per inflorescence</th><td>5.3 ± 1.5 (21)</td></tr><tr><th>Angle between peduncle and nearest flower (°)</th><td>94.7 ± 18.4 (21)</td></tr><tr><th>Angle between two outermost flowers of inflorescence (°)</th><td>145.3 ± 31.8 (21)</td></tr><tr><th>Most upright flower angle (°)</th><td>18.1 ± 10.5 (35)</td></tr><tr><th>Most downward flower angle (°)</th><td>−1.7 ± 12.6 (35)</td></tr><tr><th>Hypanthium length (mm)</th><td>26.0 ± 2.2 (20)</td></tr><tr><th>Reproductive organ length (mm)</th><td>5.55 ± 1.3 (20)</td></tr><tr><th>Nectar volume (μL)</th><td>12.8 ± 8.2 (19)</td></tr><tr><th>Sugar concentration (% brix)</th><td>18.2 ± 3.2 (19)</td></tr></tbody></table>
TABLE 2. Diagnostic characters for X. lichneuta and X in Taxonomic status of Xyrosaris melanopsamma Meyrick, 1931 (Lepidoptera: Yponomeutidae) with notes on congeneric species in East Asia
<p><b>TABLE 2.</b> Diagnostic characters for <i>X. lichneuta</i> and <i>X. melanopsamma</i> on the base of female and male genitalia.</p><table><tbody><tr><th><b>No</b></th><th><b>Diagnostic character\ species</b></th><th><i>X. lichneuta</i></th><th><i>X. melanopsamma</i></th></tr><tr><th><b>Female genitalia</b></th></tr></tbody><tbody><tr><th>1</th><td>distance between anterior edge of sterigma and posterior edge of 7th segment</td><td>relatively short, 7.6 times shorter than papillae anales</td><td>relatively long, 2.5 times shorter than papillae anales</td></tr><tr><th>2</th><td>shape of posterior edge of 7th sternite</td><td>rounded concave, with distinct lateral triangular projections</td><td>almost straight, with faintly distinguishable lateral projections</td></tr><tr><th>3</th><td>shape of sterigma</td><td>transversely oval with distinct anterior margin</td><td>more or less angular, with a weakly defined anterior edge</td></tr><tr><th>4</th><td>7th sternite</td><td>with relatively wide longitudinal zone almost lacking microsetae in the middle and sclerotised lateral sides</td><td>with close longitudinal lines of dense microsetae in the middle and weak sclerotised lateral sides</td></tr><tr><th>5</th><td>plate between base of papillae anales</td><td>as equilateral triangle</td><td>as longitudinally elongated triangle</td></tr><tr><th><b>Male genitalia</b></th></tr><tr><th>6</th><td>length of harpa</td><td>reaches 9/10 of valva length</td><td>slightly exceeds 3/5 of valva length</td></tr><tr><th>7</th><td>row of strong thorns on apical part of harpa</td><td>semioval with equal dorsal and ventral parts (Fig. 8)</td><td>arched, with longer part along ventral margin of harpa (Fig. 12)</td></tr><tr><th>3</th><td>thorns on the apical part of harpa</td><td>smaller</td><td>larger, especially along ventral margin of harpa</td></tr><tr><th>4</th><td>shape of valva</td><td>smoothly widened from base towards 3/5 (Fig. 7)</td><td>smoothly widened from base towards 1/3, further parallel-sided towards 2/3 (Fig. 11)</td></tr></tbody></table><p>......continued on the next page</p>
Table 4 in Taxonomy and trans-Beringian biogeography of the pond snails (Gastropoda: Lymnaeidae) of East Asia: an integrative view
<p><b>Table 4.</b> Conchometric characteristics of type specimens of the newly described lymnaeid species and a sample of <i>Orientogalba ollula</i>.</p><table><tbody><tr><th><b>Character /index</b></th><th><b>Species (number of measured shells)</b></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td><b><i>Galba pacifica</i> (<i>N</i> = 14)</b></td><td><i>Kamtschaticana nipponica</i></td><td><i>Orientogalba hokkaidoensis</i></td><td><i>Orientogalba ollula</i></td></tr><tr><th></th><td></td><td><b>(<i>N</i> = 5)</b></td><td><b>(<i>N</i> = 9)</b></td><td><b>(<i>N</i> = 10)</b></td></tr><tr><th>Number of whorls</th><td>4.25–5.25</td><td>3.50–4.00</td><td>4.25–5.25</td><td>3.37–5.12</td></tr><tr><th></th><td>4.72 ± 0.38</td><td>3.81 ± 0.24</td><td>4.90 ± 0.40</td><td>4.19 ± 0.45</td></tr><tr><th>Shell height (SH), mm</th><td>6.0–8.8</td><td>9.3–12.0</td><td>9.3–11.7</td><td>6.53–9.52</td></tr><tr><th></th><td>7.5 ± 1.0</td><td>10.0 ± 1.2</td><td>10.9 ± 0.7</td><td>7.50 ± 0.96</td></tr><tr><th>Shell width (SW), mm</th><td>3.5–5.2</td><td>6.5–8.4</td><td>6.1–7.3</td><td>4.07–5.69</td></tr><tr><th></th><td>3.6 ± 0.8</td><td>7.2 ± 0.8</td><td>6.7 ± 0.4</td><td>4.62 ± 0.56</td></tr><tr><th>Spire height (SpH), mm</th><td>2.3–4.7</td><td>2.2–3.9</td><td>2.2–4.2</td><td>2.18–3.76</td></tr><tr><th></th><td>3.6 ± 0.8</td><td>3.0 ± 0.7</td><td>3.6 ± 0.7</td><td>2.76 ± 0.48</td></tr><tr><th>Body whorl height (BWH), mm</th><td>4.7–6.5</td><td>8.2–10.8</td><td>7.1–9.6</td><td>4.59–7.95</td></tr><tr><th></th><td>5.7 ± 0.6</td><td>9.0 ± 1.0</td><td>8.7 ± 0.8</td><td>5.89 ± 0.85</td></tr><tr><th>Aperture height (AH), mm</th><td>3.3–4.6</td><td>6.5–8.2</td><td>5.9–7.8</td><td>4.23–7.52</td></tr><tr><th></th><td>3.9 ± 0.4</td><td>7.1 ± 0.7</td><td>7.1 ± 0.6</td><td>4.89 ± 1.02</td></tr><tr><th>Aperture width (AW), mm</th><td>2.1–3.3</td><td>6.5–8.2</td><td>4.7–5.6</td><td>2.56–3.96</td></tr><tr><th></th><td>2.7 ± 0.3</td><td>5.0 ± 0.7</td><td>5.2 ± 0.3</td><td>3.24 ± 0.42</td></tr><tr><th>Index SW/SH</th><td>0.53–0.75</td><td>0.69–0.83</td><td>0.58–0.66</td><td>0.59–0.66</td></tr><tr><th></th><td>0.60 ± 0.06</td><td>0.72 ± 0.06</td><td>0.62 ± 0.03</td><td>0.62 ± 0.02</td></tr><tr><th>Index SpH/SH</th><td>0.38–0.54</td><td>0.25–0.34</td><td>0.19–0.38</td><td>0.33–0.41</td></tr><tr><th></th><td>0.48 ± 0.04</td><td>0.29 ± 0.05</td><td>0.33 ± 0.06</td><td>0.37 ± 0.03</td></tr><tr><th>Index BWH/SH</th><td>0.72–0.83</td><td>0.88–0.95</td><td>0.62–0.87</td><td>0.62–0.84</td></tr><tr><th></th><td>0.77 ± 0.03</td><td>0.90 ± 0.02</td><td>0.80 ± 0.07</td><td>0.79 ± 0.08</td></tr><tr><th>Index AH/SH</th><td>0.45–0.63</td><td>0.65–0.76</td><td>0.62–0.73</td><td>0.59–0.85</td></tr><tr><th></th><td>0.52 ± 0.05</td><td>0.71 ± 0.05</td><td>0.65 ± 0.03</td><td>0.65 ± 0.07</td></tr><tr><th>Index AW/AH</th><td>0.61–0.85</td><td>0.62–0.78</td><td>0.66–0.83</td><td>0.49–0.75</td></tr><tr><th></th><td>0.70 ± 0.06</td><td>0.70 ± 0.07</td><td>0.73 ± 0.04</td><td>0.67 ± 0.08</td></tr></tbody></table><p>In each cell, above line,limits of variation (minimum–maximum); below line,mean value ± σ.</p>
Table 1 in Taxonomy and trans-Beringian biogeography of the pond snails (Gastropoda: Lymnaeidae) of East Asia: an integrative view
<p><b>Table 1.</b> The type series of the new lymnaeid species described in this paper.</p><table><tbody><tr><th><b>Species</b></th><th><i>N</i></th><th><b>Sampling site and date</b></th><th><b>Depository, accession number</b></th></tr></tbody><tbody><tr><th><i>Galba pacifica</i> (the holotype and a paratype)</th><td>2</td><td>Japan, Hokkaido Prefecture, Biei Town, the Ishikari River system, a ditch near the Rubeshibe Stream, 43.520331°N, 142.372452°E, 7 September 2015, leg. Y. Ohari</td><td>ZIN, no. <i>1/531-2021</i> (holotype), 3/531-2021 (paratype)</td></tr><tr><th><i>G. pacifica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Biei Town, the Ishikari River system, a ditch near the Kawamukai Stream, 43.528123°N, 142.594829°E, 7 September 2015, leg. Y. Ohari</td><td>ZIN, no. 2/531-2021</td></tr><tr><th><i>G. pacifica</i> (paratypes)</th><td>3</td><td>Japan, Hokkaido Prefecture, Hidaka Town, the Saru River system, a ditch near the Pankeusyappu Stream, 42.927325°N, 142.402711°E, 9 September 2015, leg. Y. Ohari</td><td>ZIN, no. 3/531-2021</td></tr><tr><th><i>G. pacifica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Shimukappu village, the Mukawu River system, a ditch near the Horokatomamu Stream, 43.058562°N, 142.529372°E, 8 September 2015, leg. Y. Ohari</td><td>ZIN, no. 4/531-2021</td></tr><tr><th><i>G. pacifica</i> (paratypes)</th><td>1</td><td>Japan, Hokkaido Prefecture, Shin-hidaka Town, the Shizunai River system, a ditch near the Sunbetsu Stream, 42.445675°N, 142. 549053°E, 17 September 2013, leg. Y. Ohari</td><td>RMBH, no. MLym-1113/7</td></tr><tr><th><i>G. pacifica</i> (paratypes)</th><td>1</td><td>Japan, Hokkaido Prefecture, Shin-hidaka Town, the Shizunai River system, a ditch near the Sunbetsu Stream, 42.445675°N, 142.549053°E, 17 September 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1113/6</td></tr><tr><th><i>G. pacifica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Nakagawa Town, the Teshio River system, a ditch near the Chirashinai Stream, 44.72604°N, 142.062333°E, 8 August 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1113/2</td></tr><tr><th><i>G. pacifica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Niseko Town, the Shiribetsu River system, a ditch near the Konbu Stream, 42.772299°N, 140.598945°E, 25 May 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1113/1</td></tr><tr><th><i>G. pacifica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Engaru Town, the Yubetsu River system, a ditch near the Shiyubetsu Stream, 43.862232°N, 143.189478°E, 6 September 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1113/5</td></tr><tr><th><i>G. pacifica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Naie Town, the Ishikari River system, Naie Stream, 43.391666°N, 141.975526°E, 3 September 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1113/4</td></tr><tr><th><i>G. pacifica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Wakkanai City, the Koetoi River system, Uruya Stream, 45.261444°N, 141.906737°E, 9 August 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1113/3</td></tr><tr><th><i>Kamtschaticana nipponica</i> (the holotype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Sarabetsu village, ZIN, no. <i>1/528-2021</i> the Tokachi River system, Itarataraki Stream, 42.627161°N, 143.265175°E, 3 October 2013, leg. Y. Ohari</td></tr><tr><th><i>K. nipponica</i> (paratypes)</th><td>4</td><td>Japan, Hokkaido Prefecture, Sarabetsu village, the ZIN, no. 2/528-2021 Tokachi River system, Saccharobetsu Stream, 42.627161°N, 143.265175°E, 22 June 2013, leg. Y. Ohari</td></tr><tr><th><i>K. nipponica</i> (paratypes)</th><td>3</td><td>Japan, Hokkaido Prefecture, Obihiro City, the Tokachi River system, Tobetsu Stream, 42.766686°N, 143.202864°E, 18 September 2013, leg. Y. Ohari</td><td>RMBH, no. MLym-1115/2, MLym-1115/3, and MLym-1115/4</td></tr><tr><th><i>K. nipponica</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Rankoshi Town, a ditch near the Shiribetsu River, 42.815818°N, 140.535244°E, 25 May 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1115/1</td></tr><tr><th><i>Orientogalba hokkaidoensis</i> (the holotype + paratypes)</th><td>3</td><td>Japan, Hokkaido Prefecture, Hokuto City, a ZIN, no. <i>1/530-2021</i> (holotype), ditch near the Hikirichi Stream, 41.842808°N, 2/530-2021 (paratypes) 140.634441°E, 29 June 2015, leg. Y. Ohari</td></tr><tr><th><i>O. hokkaidoensis</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Horokanai Town, the Ishikari River system, a ditch near the Uryu Stream, 44.052343°N, 142.142657°E, 4 September 2015, leg. Y. Ohari</td><td>ZIN, no. 3/530-2021</td></tr><tr><th><i>O. hokkaidoensis</i> (paratypes)</th><td>3</td><td>Japan, Hokkaido Prefecture, Tomomae Town, the Kotanbetsu River system, a ditch near the Sankebetsu River, 44.192775°N, 141.771754°E, 7 August 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1114/1, no. MLym-1114/2, and no. MLym-1114/3</td></tr><tr><th><i>O. hokkaidoensis</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Kikonai Town, the RMBH, no. MLym-1114/4 Kikonai River system, a ditch near the Uriya Stream, 41.687164°N, 140.386156°E, 29 June 2015, leg. Y. Ohari</td></tr><tr><th><i>O. hokkaidoensis</i> (a paratype)</th><td>1</td><td>Japan, Hokkaido Prefecture, Fukushima Town, a ditch near the Fukushima River, 41.490724°N, 140.250207°E, 29 June 2015, leg. Y. Ohari</td><td>RMBH, no. MLym-1114/5</td></tr></tbody></table>
Table 2 in Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus
<p>Table 2. Specimens identified as possible type material of <i>Hibiscus krichauffianus</i>, and arguments for and against nominating these samples as original material.</p><table><tbody><tr><th>Accession</th><th>Pro</th><th>Con</th><th>Decision</th></tr></tbody><tbody><tr><th>K000659853</th><td>Attributed to Babbage, a small fragment. Sent to Kew by Schomburgk in Sep.1871.</td><td>Includes fruit (label in Schomburgk’s hand).</td><td>Likely not seen by Mueller as this lacks an identification but part of original material.</td></tr><tr><th>K000659852</th><td>Annotated by Mueller.</td><td>A single fruit with seeds annotated as <i>H. krichauffii,</i> not <i>krichauffianus</i>. Dated 1885 by Mueller therefore too late for consideration.</td><td>Not a syntype.</td></tr><tr><th>AD 97611531</th><td><i>H. krichauffianus</i>, in the Schomburgk herbarium, collected in South Australia. No further collecting information. Buds and flower, no fruit.</td><td>A large branched specimen with minimal flowering material. Connection to Babbage tenuous and looks different from the material at <i>K</i>.</td><td>Probably not a syntype.</td></tr><tr><th>MEL 0068091A</th><td>Locality of Darling River, annotated by Mueller as <i>H. krichauffianus</i>, collected by Goodwin. Mentioned in protologue.</td><td>A collection of six small fragments, one of which has a young capsule. Description in protologue does not (appear to) encompass these.</td><td>Syntype, as part of the type gathering but not material used in describing the species.</td></tr><tr><th>Herb. F. Mueller: five branches from different collectors mounted on same K sheet as those above. Without barcode.</th><td>Herbarium of the author of the species. Includes a specimen locality of Darling River. All but the one on the right have flowers and no fruit. These specimens are all from the Mueller Herb. Bentham cites a Babbage collection in <i>Flora australiensis</i> supporting the concept that one of these five is the original Babbage collection used by Mueller.</td><td>As discussed in text, specimens 1, 2, and 5 can be excluded. Either or both specimens 3 and 4 represent original material used by Mueller to describe the species and could be chosen.</td><td>Specimens 3 and 4 are possible syntypes, possibly matching either the Babbage or Goodwin material.</td></tr></tbody></table>
Table 3 in Plastid phylogenomics of the Eriostemon group (Rutaceae; Zanthoxyloideae): support for major clades and investigation of a backbone polytomy
<p>Table 3. Alignment Information.</p><table><tbody><tr><th>Item</th><th>Number of variable sites</th><th>Number of parsimony-informative sites</th><th>Number of constant sites</th><th>Total length (bp)</th></tr></tbody><tbody><tr><th>Phylogenomic alignment</th><td>30 038</td><td>16 845</td><td>76 847</td><td>106 885</td></tr><tr><th>Supermatrix alignment</th><td>30 057</td><td>16 895</td><td>76 657</td><td>106 714</td></tr></tbody></table>
Table 2 in Plastid phylogenomics of the Eriostemon group (Rutaceae; Zanthoxyloideae): support for major clades and investigation of a backbone polytomy
<p>Table 2. Taxonomic coverage of sampling from the <i>Eriostemon</i> group.</p><table><tbody><tr><th>Genus</th><th>Section</th><th>Number of species sampled (full plastome data)</th><th>Number of species sampled (Sanger data)</th><th>Total number of species</th></tr></tbody><tbody><tr><th><i>Asterolasia</i></th><td></td><td>2</td><td></td><td>19</td></tr><tr><th><i>Chorilaena</i></th><td></td><td>3</td><td></td><td>4</td></tr><tr><th><i>Correa</i></th><td></td><td>3</td><td></td><td>11</td></tr><tr><th><i>Crowea</i></th><td></td><td>3</td><td></td><td>3</td></tr><tr><th><i>Diplolaena</i></th><td></td><td>2</td><td></td><td>15</td></tr><tr><th><i>Drummondita</i></th><td></td><td>3</td><td>(1)</td><td>11</td></tr><tr><th><i>Eriostemon</i></th><td></td><td>2</td><td></td><td>2</td></tr><tr><th><i>Geleznowia</i></th><td></td><td>1</td><td>(1)</td><td>2</td></tr><tr><th><i>Halfordia</i></th><td></td><td>1</td><td></td><td>1–3</td></tr><tr><th><i>Leionema</i></th><td></td><td>4</td><td></td><td>28</td></tr><tr><th><i>Muiriantha</i></th><td></td><td>1</td><td></td><td>1</td></tr><tr><th><i>Myrtopsis</i></th><td></td><td>1</td><td></td><td>~9</td></tr><tr><th><i>Nematolepis</i></th><td></td><td>3</td><td></td><td>7</td></tr><tr><th><i>Neoschmidia</i></th><td></td><td>1</td><td></td><td>2</td></tr><tr><th><i>Phebalium</i></th><td></td><td>7</td><td></td><td>38</td></tr><tr><th><i>Philotheca</i></th><td><i>Corynonema</i></td><td>3</td><td></td><td>3</td></tr><tr><th></th><td><i>Cyanochlamys</i></td><td>2</td><td></td><td>2</td></tr><tr><th></th><td><i>Erionema</i></td><td>2</td><td>2</td><td>15</td></tr><tr><th></th><td><i>Philotheca</i></td><td>4</td><td>20 (2)</td><td>34</td></tr><tr><th>Total</th><td></td><td>48</td><td>22 (4)</td><td>~206–209</td></tr></tbody></table><p>Numbers in parentheses indicate where the same species was sampled in both the full plastome and Sanger datasets. Total number of species includes described taxa only (i.e. phrase-named species are excluded).</p>
Table 1. Morphological diagnostic characters delimiting H in Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus
<p>Table 1. Morphological diagnostic characters delimiting <i>H. krichauffianus</i> sens. strict., and the three new entities.</p><table><tbody><tr><th>Character</th><th>Morphotype A – <i>Hibiscus krichauffianus</i></th><th>Morphotype B – <i>Hibiscus verecundus</i></th><th>Morphotype C – <i>Hibiscus calcareus</i></th><th>Morphotype D – <i>Hibiscus</i> sp. Belele (D.W.Goodall 3417)</th></tr></tbody><tbody><tr><th>Substrate preference</th><td>Deep sand</td><td>Typically shallow soils over sandstone, laterite or basalt</td><td>Lime-rich soils</td><td>Insufficient data</td></tr><tr><th>Plant habit</th><td>Subshrub or shrub to ~1 m high, usually erect or ascending</td><td>Low spreading subshrub or shrub to ~0.5 m high, usually decumbent</td><td>Low subshrub to ~0.5 m high, spreading, dome-shaped or rounded</td><td>Low or dwarf subshrub or shrub to ~0.3 m high</td></tr><tr><th>Branchlet indumentum colour</th><td>Silvery-white, white, sometimes fading to yellowish-white</td><td>Yellowish-brown, sometimes fading to white</td><td>White, or silvery-white</td><td>White on younger branchlets, older branchlets becoming ferruginous (ferruginous rays and white rays sometimes on the same hair)</td></tr><tr><th>Stipule width (mm)</th><td>0.16–0.4</td><td>0.1–0.17</td><td>0.2–0.5</td><td>0.2–0.35</td></tr><tr><th>Leaf lamina colour (adaxial)</th><td>Whitish-silver to grey, becoming greyish-green with age</td><td>Green to dark green</td><td>Grey to silvery-white</td><td>Silvery–ferruginous</td></tr><tr><th>Leaf lamina shape</th><td>Mostly ovate to lanceolate or oblong, occasionally broadly ovate</td><td>Ovate to broadly ovate, rarely elliptic–ovate</td><td>Ovate, elliptic–ovate or oblong–ovate</td><td>Ovate to elliptic–ovate</td></tr><tr><th>Leaf lamina in transverse</th><td>Flat to weakly concave or weakly folded</td><td>Flat to weakly concave or weakly folded</td><td>Mostly strongly concave to vshaped (and appearing folded on many herbarium specimens)</td><td>Flat to weakly folded</td></tr><tr><th>Leaf lamina length and width (mm)</th><td>10–55 × 5–35</td><td>9–52 × 8–33</td><td>6–28 × 4–16</td><td>17–43 × 6–22</td></tr><tr><th>Leaf lamina base</th><td>Obtuse, truncate or very broadly cuneate</td><td>Broadly cuneate, obtuse or truncate</td><td>Broadly cuneate or truncate</td><td>Truncate, very slightly cordate or broadly obtuse</td></tr><tr><th>Leaf lamina margin</th><td>Crenate to dentate</td><td>Serrate to dentate, rarely crenate</td><td>Serrate to dentate or crenate, undulate, sinus between teeth up to halfway to midvein</td><td>Dentate to crenate</td></tr><tr><th>Abcision line (at peduncle–pedicel junction), whether visible and position</th><td>Not obvious, obscured by hairs, usually 1–2 mm from the base, rarely up to one-half length from the base</td><td>Sometimes obvious, one-third to one-half length from the base</td><td>±Obvious, sometimes obscured by hairs, usually in upper half, 2–17 (–24) mm from the base</td><td>±Obvious, sometimes obscured by hairs, approximately one-third length from the base</td></tr><tr><th>Number of epicalyx lobes</th><td>5–8 (rarely 10, rarely bifurcating)</td><td>5–7</td><td>7–8</td><td>5–6</td></tr><tr><th>Epicalyx length (Including fused portion, excluding receptacle) (mm)</th><td>7–16</td><td>6–10</td><td>4–14</td><td>6–12</td></tr><tr><th>Fusion of epicalyx lobes at base</th><td>Fused for 1–4 mm</td><td>Free or fused to 0.5 mm</td><td>Fused for 1–3.5 mm</td><td>Free or fused for up to 1 mm</td></tr><tr><th>Epicalyx lobes degree of curvature</th><td>Straight in flower, becoming recurved or rarely incurved in fruit</td><td>Straight</td><td>Straight in flower, becoming recurved in fruit</td><td>Straight in flower, becoming recurved in fruit</td></tr><tr><th>Corolla colour</th><td>Pale pink or mauve (rarely white)</td><td>Pale pink or white (sometimes drying pale yellow)</td><td>Pale pink to mauve, sometimes almost white</td><td>Purple</td></tr><tr><th>Petal length (mm)</th><td>17–35</td><td>15–28</td><td>20–44</td><td>39–42</td></tr><tr><th>Seed indumentum</th><td>Patchy indumentum of wispy spreading, white to off-white hairs</td><td>Short patchy indumentum of appressed white to yellowish-brown hairs</td><td>Short patchy indumentum of appressed white hairs</td><td>Short patchy indumentum of appressed white to yellowish hairs</td></tr><tr><th>Seed length (mm, greatest dimension)</th><td>2–3</td><td>1.7–2.3</td><td>2.5–3</td><td>~3</td></tr><tr><th>Seed characteristic features or notes</th><td>Reniform (rarely subangular–reniform), funicular remnants brown, membranous and wing-like, on either side of the hilum</td><td>Two straighter sides almost forming a right angle at intersection, funicular remnants brown, membranous and wing-like, one centrally placed and one on either side of the hilum</td><td>Two straighter sides almost forming a right angle at intersection, funicular remnants brown, membranous and wing-like, on either side of the hilum</td><td>Two straighter sides almost forming a right angle at intersection, funicular remnants brown, membranous and wing-like, on either side of the hilum</td></tr><tr><th>Flower cleistogamy</th><td>Observed in some specimens</td><td>No evidence</td><td>Observed in a single specimen</td><td>Not observed in material examined</td></tr></tbody></table>
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