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TABLE 2 in Canines make the difference: a new species of Hypsugo (Chiroptera: Vespertilionidae) from Laos and Vietnam
<p><b>TABLE 2</b>. Factor loadings of craniodental characters obtained by the PCA.</p><table><tbody><tr><th>Character</th><th>PC1</th><th>PC2</th><th>PC3</th></tr></tbody><tbody><tr><th>GLS-i</th><td>0.837</td><td>-0.140</td><td>0.105</td></tr><tr><th>GLS</th><td>0.871</td><td>-0.291</td><td>0.054</td></tr><tr><th>CCL</th><td>0.932</td><td>-0.202</td><td>-0.032</td></tr><tr><th>C1C1W</th><td>0.678</td><td>-0.167</td><td>0.156</td></tr><tr><th>M3M3W</th><td>0.862</td><td>-0.142</td><td>0.057</td></tr><tr><th>IOW</th><td>0.418</td><td>0.648</td><td>0.355</td></tr><tr><th>MAW</th><td>0.724</td><td>0.483</td><td>-0.08</td></tr><tr><th>BCW</th><td>0.515</td><td>0.672</td><td>0.306</td></tr><tr><th>BCH</th><td>0.575</td><td>-0.527</td><td>0.398</td></tr><tr><th>CM3L</th><td>0.886</td><td>0.114</td><td>-0.297</td></tr><tr><th>CP4L</th><td>0.682</td><td>-0.056</td><td>-0.600</td></tr><tr><th>ML</th><td>0.857</td><td>-0.039</td><td>-0.064</td></tr><tr><th>cm3L</th><td>0.840</td><td>0.270</td><td>-0.296</td></tr><tr><th>CPH</th><td>0.765</td><td>-0.166</td><td>0.313</td></tr><tr><th>Eigenvalue</th><td>8.101</td><td>1.693</td><td>1.064</td></tr><tr><th>Percentage of variance (%)</th><td>57.9</td><td>12.1</td><td>7.6</td></tr></tbody></table>
TABLE 2 in Carabus of Subgenus Cathoplius C. G. Thomson, 1875, with description of their life-way, life-cycle and pre-imaginal morphology (Coleoptera: Carabidae)
<p><b>TABLE 2.</b> Minimum and maximum length of the three larval instars of the species and subspecies of Subgenus <i>Cathoplius</i>.</p><table><tbody><tr><th>Taxon</th><th>1st instar larva minimum and maximum length (mm)</th><th>2nd instar larva minimum and maximum length (mm)</th><th>3rd instar larva minimum and maximum length (mm)</th></tr></tbody><tbody><tr><th><i>C. asperatus</i> (Dejean, 1826)</th><td>9.2÷13.9</td><td>13.0÷20.0</td><td>19.2÷29.0</td></tr><tr><th><i>C. stenocephalus stenocephalus</i> Lucas, 1866</th><td>8.8÷14.0</td><td>13.4÷20.4</td><td>20.1÷29.8</td></tr><tr><th><i>C. stenocephalus susicus</i> Antoine, 1941</th><td>10.0÷14.3</td><td>14.0÷22.0</td><td>20.0÷32.0</td></tr><tr><th><i>C. stenocephalus ifniensis</i> Zarco, 1941</th><td>11.0÷18.0</td><td>17.0÷25.0</td><td>23.0÷35.0</td></tr><tr><th><i>C. stenocephalus aliai</i> Escalera, 1944</th><td>9.5÷16.5</td><td>16.0÷21.5</td><td>22.0÷30.0</td></tr></tbody></table>
TABLE 1 in Carabus of Subgenus Cathoplius C. G. Thomson, 1875, with description of their life-way, life-cycle and pre-imaginal morphology (Coleoptera: Carabidae)
<p><b>TABLE 1.</b> Total number of laid eggs per female, oviposition period and oviposition rate in Subgenus <i>Cathoplius</i>.</p><table><tbody><tr><th>Taxon</th><th>♀♀</th><th>Total no. of laid eggs</th><th>Oviposition period</th><th>Oviposition rate (eggs/day)</th></tr></tbody><tbody><tr><th><i>C. asperatus</i> (Dejean, 1826)</th><td>1st ♀</td><td>241</td><td>from 30/11/2008 to 23/01/2009</td><td>4.46</td></tr><tr><th><i>C. stenocephalus stenocephalus</i> Lucas, 1866</th><td>1st ♀</td><td>288</td><td>from 30/11/2008 to 18/01/2009</td><td>5.88</td></tr><tr><th><i>C. stenocephalus susicus</i> Antoine, 1941</th><td>1st ♀</td><td>511</td><td>from 30/11/2008 to 10/01/2009</td><td>12.46</td></tr><tr><td>2nd ♀</td><td>423</td><td>from 30/11/2008 to 10/03/2009</td><td>4.23</td></tr><tr><th><i>C. stenocephalus ifniensis</i> Zarco, 1941</th><td>1st ♀</td><td>342</td><td>from 30/11/2008 to 12/01/2009</td><td>7.95</td></tr><tr><th><i>C. stenocephalus aliai</i> Escalera, 1944</th><td>1st ♀</td><td>302</td><td>from 28/12/2010 to 02/04/2011</td><td>3.51</td></tr><tr><td>2nd ♀</td><td>261</td><td>from 30/11/2011 to 01/03/2012</td><td>2.87</td></tr><tr><td>3rd ♀</td><td>289</td><td>from 30/11/2011 to 22/02/2012</td><td>3.44</td></tr></tbody></table>
TABLE 1 in Canines make the difference: a new species of Hypsugo (Chiroptera: Vespertilionidae) from Laos and Vietnam
<p><b>TABLE 1</b>. Selected external and craniodental measurements (in mm) of <i>H. pulveratus</i> and <i>H. dolichodon</i> <b>n. sp.</b> Values are given as mean, ± SD (n ≥ 2), min-max, (n). Acronyms and definitions for measurements are given in the text.</p><table><tbody><tr><th>character</th><th><i>H. pulveratus</i></th><th><i>H. pulveratus</i> ♂</th><th><i>H. pulveratus</i> ♀</th><th><i>H. dolichodon</i> <b>n.sp.</b></th></tr></tbody><tbody><tr><th>FA</th><td>34.6 ± 1.39 32.4–37.6 (32)</td><td>34.2 ± 0.99 32.4–35.8 (19)</td><td>35.4 ± 1.63 32.4–37.6 (11)</td><td>37.0 ± 1.30 35.2–38.4 (4)</td></tr><tr><th>TIB</th><td>13.9 ± 0.53 12.9–14.7 (11)</td><td>13.7 ± 0.42 13.0–14.1 (5)</td><td>14.0 ± 0.62 12.9–14.7 (6)</td><td>14.4 ± 0.20 14.2–14.5 (2)</td></tr><tr><th>HF</th><td>6.1 ± 0.79 4.7–8.2 (24)</td><td>6.0 ± 0.81 4.7–8.0 (14)</td><td>6.3 ± 0.78 5.4–8.2 (10)</td><td>6.4 ± 0.50 5.9–7.0 (4)</td></tr><tr><th>GLS-i</th><td>14.01 ± 0.38 13.26–14.64 (26)</td><td>13.89 ± 0.38 13.26–14.28 (11)</td><td>14.12 ± 0.40 13.32–14.64 (13)</td><td>14.25 ± 0.43 13.83–14.83 (4)</td></tr><tr><th>GLS</th><td>13.75 ± 0.25 13.26–14.11 (26)</td><td>13.66 ± 0.22 13.26–13.94 (11)</td><td>13.81 ± 0.27 13.32–14.11 (13)</td><td>13.76 ± 0.41 13.30–14.29 (4)</td></tr><tr><th>CCL</th><td>12.63 ± 0.30 12.00–13.20 (28)</td><td>12.53 ± 0.22 12.12–12.81 (12)</td><td>12.75 ± 0.31 12.00–13.20 (13)</td><td>12.86 ± 0.36 12.45–13.31 (4)</td></tr><tr><th>C1C1W</th><td>4.22 ± 0.19 3.72–4.53 (30)</td><td>4.27 ± 0.18 4.00–4.53 (12)</td><td>4.20 ± 0.20 3.72–4.42 (14)</td><td>4.17 ± 0.19 4.00–4.40 (4)</td></tr><tr><th>M3M3W</th><td>5.73 ± 0.21 5.20–6.11 (29)</td><td>5.69 ± 0.13 5.34–5.83 (11)</td><td>5.78 ± 0.26 5.20–6.11 (14)</td><td>5.77 ± 0.20 5.52–6.00 (4)</td></tr><tr><th>RW</th><td>4.95 ± 0.22 4.53–5.45 (30)</td><td>4.95 ± 0.18 4.62–5.24 (12)</td><td>4.95 ± 0.26 4.53–5.45 (14)</td><td>5.20 ± 0.35 4.87–5.65 (4)</td></tr><tr><th>IOW</th><td>3.73 ± 0.15 3.33–3.99 (31)</td><td>3.75 ± 0.14 3.50–3.97 (12)</td><td>3.70 ± 0.17 3.33–3.99 (15)</td><td>3.86 ± 0.06 3.77–3.90 (4)</td></tr><tr><th>ZYW</th><td>8.46 ± 0.18 8.15–8.80 (21)</td><td>8.39 ± 0.15 8.16–8.62 (11)</td><td>8.52 ± 0.20 8.15–8.80 (8)</td><td>8.43 ± 0.35 8.18–8.68 (2)</td></tr><tr><th>MAW</th><td>7.24 ± 0.13 6.94–7.56 (27)</td><td>7.23 ± 0.12 7.00–7.37 (12)</td><td>7.27 ± 0.15 6.94–7.56 (12)</td><td>7.66 ± 0.14 7.47–7.77 (4)</td></tr><tr><th>BCW</th><td>6.75 ± 0.16 6.18–6.97 (27)</td><td>6.79 ± 0.12 6.58–6.97 (11)</td><td>6.72 ± 0.20 6.18–6.96 (13)</td><td>6.97 ± 0.17 6.79–7.12 (3)</td></tr><tr><th>BCH</th><td>4.81 ± 0.13 4.62–5.10 (25)</td><td>4.78 ± 0.10 4.62–4.97 (10)</td><td>4.82 ± 0.15 4.62–5.10 (12)</td><td>4.84 ± 0.15 4.67–5.04 (4)</td></tr><tr><th>AOB</th><td>0.85 ± 0.19 0.54–1.17 (22)</td><td>0.87 ± 0.14 0.76–1.10 (7)</td><td>0.87 ± 0.21 0.54–1.17 (13)</td><td>0.96 ± 0.07 0.92–1.06 (4)</td></tr><tr><th>CM3L</th><td>4.88 ± 0.14 4.57–5.15 (33)</td><td>4.87 ± 0.14 4.62–5.11 (14)</td><td>4.91 ± 0.14 4.64–5.15 (15)</td><td>5.05 ± 0.15 4.84–5.19 (4)</td></tr><tr><th>CP4L</th><td>1.99 ± 0.12 1.66–2.23 (33)</td><td>2.01 ± 0.11 1.81–2.17 (14)</td><td>1.97 ± 0.14 1.66–2.23 (15)</td><td>2.09 ± 0.20 1.80–2.24 (4)</td></tr><tr><th>ML</th><td>9.65 ± 0.21 9.15–9.96 (31)</td><td>9.59 ± 0.18 9.29–9.92 (14)</td><td>9.75 ± 0.15 9.50–9.96 (14)</td><td>10.00 ± 0.28 9.59–10.21 (4)</td></tr><tr><th>cm3L</th><td>5.20 ± 0.14 4.86–5.47 (33)</td><td>5.19 ± 0.14 4.98–5.47 (14)</td><td>5.24 ± 0.13 5.01–5.39 (15)</td><td>5.49 ± 0.14 5.34–5.65 (4)</td></tr><tr><th>CPH</th><td>2.75 ± 0.11 2.52–3.02 (33)</td><td>2.71 ± 0.09 2.52–2.85 (14)</td><td>2.79 ± 0.13 2.58–3.02 (15)</td><td>2.90 ± 0.20 2.72–3.11 (3)</td></tr></tbody></table>
Table 1 in The first known riodinid ' cuckoo' butterfly reveals deep-time convergence and parallelism in ant social parasites
<p><b>Table 1.</b> Homoplastic ecomorphological traits shared between <i>Aricoris arenarum</i> (Riodinidae) and <i>Niphanda fusca</i> (Lycaenidae) (for details, see Fig. 8 and Discussion)</p><table><tbody><tr><th>Ecomorphological trait</th><th>Potential type of homoplasy</th><th>Hypothetical adaptive significance</th></tr></tbody><tbody><tr><th>Ant–hemipteran-dependent oviposition</th><td>Convergence</td><td>Increases the likelihood of interaction</td></tr><tr><th>Loss of plant specificity and oviposition on Poaceae</th><td>Convergence</td><td>Exploitation of new ant–plant– hemipteran systems</td></tr><tr><th>Feed on liquids (hemipteran honeydew and ant regurgitations)</th><td>Convergence</td><td>Reduction of symbiotic cost by not feeding directly on plant tissue, hemipterans or ants</td></tr><tr><th>Social parasitism</th><td>Convergence</td><td>Stable and enemy-free environment (ant nest) during cold months and nutritional benefits</td></tr><tr><th>Pinkish last instar caterpillars</th><td>Convergence</td><td>Lack of plant pigments and/or no selection for visual crypsis</td></tr><tr><th>Long thoracic setae directed forwards</th><td>Parallelism and convergence</td><td>Tactile communication with hemipterans and ants</td></tr><tr><th>Reduction of dorsal setae on metathorax</th><td>Parallelism</td><td>Improved mobility of the anterior portion, facilitating ant trophallaxis</td></tr><tr><th>Tentacle organs on eighth abdominal segment</th><td>Convergence and parallelism</td><td>Chemical communication with tending ants</td></tr></tbody></table>
Table 1 in Anatomy and phylogenetic relationships of Temnodontosaurus zetlandicus (Reptilia: Ichthyosauria)
<p><b>Table 1.</b> Measurements (anteroposterior length, diameter, dorsoventral height, mediolateral width) of <i>Temnodontosaurus zetlandicus</i> comb. nov. (holotype CAMSM J35176) and <i>Temnodontosaurus</i> cf. <i>zetlandicus</i> (MNHNL TU885)</p><table><tbody><tr><th>Measurements (in mm)</th><th>CAMSM J35176</th><th>MNHNL TU885</th></tr></tbody><tbody><tr><th>Length of the skull (estimation)</th><td>990</td><td>–</td></tr><tr><th>Length of the rostrum (estimation)</th><td>680</td><td>–</td></tr><tr><th>Length of the pre-naris rostrum (estimation)</th><td>544</td><td>–</td></tr><tr><th>Height of the left orbit</th><td>160</td><td>–</td></tr><tr><th>Length of the left orbit</th><td>195</td><td>–</td></tr><tr><th>Height of the right orbit</th><td>164</td><td>–</td></tr><tr><th>Length of the right orbit</th><td>201</td><td>–</td></tr><tr><th>Height of the left sclerotic ring</th><td>–</td><td>165</td></tr><tr><th>Length of the left sclerotic ring</th><td>–</td><td>159</td></tr><tr><th>Length of the left supratemporal fenestra</th><td>165</td><td>–</td></tr><tr><th>Length of the right supratemporal fenestra</th><td>~149</td><td>147</td></tr><tr><th>Length of the left naris</th><td>109</td><td>–</td></tr><tr><th>Length of the right naris</th><td>112</td><td>–</td></tr><tr><th>Length of the parietal foramen</th><td>30</td><td>28</td></tr><tr><th>Width of the parietal foramen</th><td>10</td><td>20</td></tr><tr><th>Length of the left postorbital region</th><td>106</td><td>89</td></tr><tr><th>Length of the right postorbital region</th><td>95</td><td>–</td></tr><tr><th>Length of the parietal</th><td>173</td><td>152</td></tr><tr><th>Length of the frontal</th><td>125</td><td>~120</td></tr><tr><th>Height of the basioccipital</th><td>–</td><td>102</td></tr><tr><th>Width of the basioccipital</th><td>90</td><td>103</td></tr><tr><th>Height of the basioccipital condyle</th><td>_</td><td>61</td></tr><tr><th>Width of the basioccipital condyle</th><td>66</td><td>78</td></tr></tbody></table>
Table 2 in Descriptive skeletal anatomy of Blommersia transmarina (Amphibia: Anura: Mantellidae) from the Comoro Islands
<p>Table 2 Descriptive statistics and sexual dimorphism of the 123 skeletal measures taken on 10 specimens (five male / five female) of <i>Blommersia transmarina</i>. Measures are partitioned into anatomical regions to facilitate lecture:SVL,skull, pectoral girdle, forelimb, vertebral column, pelvic girdle, and hind limb. Significant differences in mean length between males and females (α = 0.05) are shown in bold.Abbreviations follow those in the description of the measurements (Appendix 1) (<i>cont.</i>).</p><table><tbody><tr><th>(mm)</th><th></th><th>N</th><th>range</th><th>min</th><th>max</th><th>Sexual dimorphism</th><th>partial eta-squared</th><th>Median Mean</th><th>sd</th><th>Asymmetry</th><th>Kurtosis</th></tr></tbody><tbody><tr><th>foot_tph1L</th><td>10</td><td>.24</td><td>.39</td><td>.63</td><td></td><td></td><td>.49</td><td>.49</td><td>.0662</td><td>.65</td><td>1.24</td></tr><tr><th></th><td>F M</td><td>5 5</td><td></td><td></td><td></td><td>0.383</td><td>0.10</td><td></td><td>.51.47</td><td>.0876.0353</td><td></td><td></td></tr><tr><th>foot_D1</th><td></td><td>10</td><td>1.46</td><td>3.26</td><td>4.72</td><td></td><td></td><td>3.80</td><td>3.82</td><td>.4315</td><td>.81</td><td>.86</td></tr><tr><th></th><td>F M</td><td>5 5</td><td></td><td></td><td></td><td>0.560</td><td>0.04</td><td></td><td>3.91 3.74</td><td>.5827.2469</td><td></td><td></td></tr><tr><th>foot_ph2L1</th><td>10</td><td>.67</td><td>1.65</td><td>2.32</td><td></td><td></td><td>1.75</td><td>1.83</td><td>.2101</td><td>1.59</td><td>2.59</td></tr><tr><th></th><td>F M</td><td>5 5</td><td></td><td></td><td></td><td>0.226</td><td>0.18</td><td></td><td>1.91 1.74</td><td>.2795.0603</td><td></td><td></td></tr><tr><th>foot_tph2L</th><td>10</td><td>.23</td><td>.49</td><td>.72</td><td></td><td></td><td>.56</td><td>.57</td><td>.0642</td><td>1.58</td><td>4.08</td></tr><tr><th></th><td>F M</td><td>5 5</td><td></td><td></td><td></td><td>0.410</td><td>0.09</td><td></td><td>.59.55</td><td>.0836.0386</td><td></td><td></td></tr><tr><th>foot_D2</th><td></td><td>10</td><td>2.14</td><td>5.82</td><td>7.96</td><td></td><td></td><td>6.33</td><td>6.46</td><td>.6259</td><td>1.68</td><td>3.39</td></tr><tr><th></th><td>F M</td><td>5 5</td><td></td><td></td><td></td><td>0.210</td><td>0.19</td><td></td><td>6.72 6.20</td><td>.8114.2383</td><td></td><td></td></tr><tr><th>foot_ph3L1</th><td>10</td><td>.81</td><td>2.20</td><td>3.02</td><td></td><td></td><td>2.42</td><td>2.47</td><td>.2669</td><td>1.03</td><td>.41</td></tr><tr><th></th><td>F M</td><td>5 5</td><td></td><td></td><td></td><td>0.133</td><td>0.26</td><td></td><td>2.60 2.35</td><td>.3258.1121</td><td></td><td></td></tr><tr><th>foot_ph3L2</th><td>10</td><td>.50</td><td>1.50</td><td>2.01</td><td></td><td></td><td>1.59</td><td>1.65</td><td>.1619</td><td>1.32</td><td>1.48</td></tr><tr><th></th><td>F M</td><td>5 5</td><td></td><td></td><td></td><td>0.162</td><td>0.23</td><td></td><td>1.72 1.57</td><td>.1994.0756</td><td></td><td></td></tr></tbody></table>
Table 2 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
<p><b>Table 2.</b> List of voucher specimens used for molecular-genetic analyses. All type specimens are located at the CeNak, Universität Hamburg (ZMH catalogue), while voucher specimens of undescribed species are located at the DZMB, Hamburg</p><table><tbody><tr><th>Voucher ID #</th><th>Voyage</th><th>Area</th><th>Station</th><th>Species</th><th>Marker</th><th>GenBank accession #</th><th>Collection #</th><th>Sex</th></tr></tbody><tbody><tr><th>Na43</th><td>AB02</td><td>OMS*</td><td>S11</td><td><i>Nannoniscus</i> sp.</td><td>16S</td><td>MT259290</td><td>DZMB-69115</td><td>F</td></tr><tr><th>Na37</th><td>AB02</td><td>OMS</td><td>S11</td><td><i>Nannoniscus</i> sp.</td><td>16S</td><td>MT259291</td><td>DZMB-69116</td><td>F</td></tr><tr><th>Na39</th><td>AB02</td><td>OMS</td><td>S11</td><td><i>Nannoniscus</i> sp.</td><td>16S</td><td>MT259292</td><td>DZMB-69117</td><td>F</td></tr><tr><th>AB2ISO431</th><td>AB02</td><td>OMS</td><td>S5</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>MT256412</td><td>DZMB-69118</td><td>F</td></tr><tr><th>AB2ISO442</th><td>AB02</td><td>UK</td><td>U7</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>MT256413</td><td>DZMB-69119</td><td>M</td></tr><tr><th>Na41</th><td>AB02</td><td>OMS</td><td>S10</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>MT256414</td><td>DZMB-69120</td><td>F</td></tr><tr><th>NB12_Iso020</th><td>BIONOD</td><td>GER</td><td>06</td><td><i>N. hilario</i></td><td><i>COI</i></td><td>KJ736105</td><td>ZMH K-55341</td><td>F</td></tr><tr><th>Na25</th><td>JPIO</td><td>GER PA</td><td>24</td><td><i>N. hilario</i></td><td><i>COI</i>,</td><td>MT256415</td><td>ZMH K-55381</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259293</td><td></td><td></td></tr><tr><th>Na23</th><td>JPIO</td><td>GER PA</td><td>24</td><td><i>N. hilario</i></td><td><i>COI</i></td><td>MT256416</td><td>ZMH K-55342</td><td>F</td></tr><tr><th>NB12_Iso445</th><td>BIONOD</td><td>FRA</td><td>101</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>KJ736107</td><td>DZMB-69121</td><td>F</td></tr><tr><th>Na14</th><td>JPIO</td><td>FRA</td><td>158</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>MT256417</td><td>DZMB-69124</td><td>F</td></tr><tr><th>NB12_Iso098</th><td>BIONOD</td><td>FRA</td><td>67</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>KJ736106</td><td>DZMB-69122</td><td>F</td></tr><tr><th>Na16</th><td>JPIO</td><td>FRA</td><td>158</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>MT256418</td><td>DZMB-69125</td><td>M</td></tr><tr><th>Na20</th><td>JPIO</td><td>GSR</td><td>133</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i>,</td><td>MT256419</td><td>DZMB-69126</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259294</td><td></td><td></td></tr><tr><th>MA13_Iso453</th><td>MA13</td><td>GER PRZ</td><td>90</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>MT256420</td><td>ZMH K-55348</td><td>F</td></tr><tr><th>Iso1005/Na40</th><td>AB02</td><td>OMS</td><td>S11</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>MT256421</td><td>ZMH K-55349</td><td>F</td></tr><tr><th>MA14_Iso272</th><td>MA14</td><td>GER PRZ</td><td>38</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>MT256422</td><td>ZMH K-55350</td><td>M</td></tr><tr><th>MA14_Iso352</th><td>MA14</td><td>GER PRZ</td><td>39</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>MT256423</td><td>ZMH K-55351</td><td>F</td></tr><tr><th>Na06</th><td>JPIO</td><td>GSR</td><td>117</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>MT256424</td><td>ZMH K-55352</td><td>F</td></tr><tr><th>NB12_Iso068</th><td>BIONOD</td><td>GER</td><td>33</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>KJ736104</td><td>ZMH K-55353</td><td>F</td></tr><tr><th>Na27</th><td>JPIO</td><td>FRA</td><td>171</td><td><i>N. menoti</i></td><td><i>COI</i>,</td><td>MT256425</td><td>ZMH K-55354</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259295</td><td></td><td></td></tr><tr><th>Iso1120/Na42</th><td>AB02</td><td>APEI-6</td><td>APEI-6#1</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>MT256426</td><td>ZMH K-55355</td><td>F</td></tr><tr><th>Na18</th><td>JPIO</td><td>GER PA</td><td>20</td><td><i>N. menoti</i></td><td><i>COI</i></td><td>MT256427</td><td>ZMH K-55356</td><td>F</td></tr><tr><th>MA13_Iso049</th><td>MA13</td><td>GER PA</td><td>07</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>MT256428</td><td>ZMH K-55357</td><td>F</td></tr><tr><th>Na08</th><td>JPIO</td><td>GSR</td><td>133</td><td><i>N. pedro</i></td><td><i>COI</i>,</td><td>MT256429</td><td>ZMH K-55358</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259296</td><td></td><td></td></tr><tr><th>MA13_Iso593</th><td>MA13</td><td>GER PRZ</td><td>90</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>MT256430</td><td>ZMH K-55359</td><td>F</td></tr><tr><th>NB12_Iso290</th><td>BIONOD</td><td>GER</td><td>43</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>KJ736102</td><td>ZMH K-55360</td><td>F</td></tr><tr><th>Na04</th><td>JPIO</td><td>GER PA</td><td>20</td><td><i>N. pedro</i></td><td><i>COI</i>,</td><td>MT256431</td><td>ZMH K-55361</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259297</td><td></td><td></td></tr><tr><th>Na11</th><td>JPIO</td><td>FRA</td><td>171</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>MT256432</td><td>ZMH K-55362</td><td>F</td></tr><tr><th>Na22</th><td>JPIO</td><td>GER PA</td><td>24</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>MT256433</td><td>ZMH K-55363</td><td>F</td></tr><tr><th>NB12_Iso330</th><td>BIONOD</td><td>GER</td><td>43</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>KJ736103</td><td>ZMH K-55364</td><td>F</td></tr><tr><th>Na05</th><td>JPIO</td><td>GER PA</td><td>20</td><td><i>N. pedro</i></td><td><i>COI</i>,</td><td>MT256434</td><td>ZMH K-55365</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259298</td><td></td><td></td></tr><tr><th>MA14_Iso242</th><td>MA14</td><td>GER PRZ</td><td>39</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>MT256435</td><td>ZMH K-55366</td><td>M</td></tr><tr><th>MA14_Iso319</th><td>MA14</td><td>GER PRZ</td><td>39</td><td><i>N. pedro</i></td><td><i>COI</i></td><td>MT256436</td><td>ZMH K-55367</td><td>F</td></tr><tr><th>MA14_Iso258</th><td>MA14</td><td>GER IRZ</td><td>21</td><td><i>N. brenkei</i></td><td><i>COI</i></td><td>MT256437</td><td>ZMH K-55368</td><td>M?</td></tr><tr><th>Na03</th><td>JPIO</td><td>GER PA</td><td>20</td><td><i>N. brenkei</i></td><td><i>COI</i>,</td><td>MT256438</td><td>ZMH K-55369</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259299</td><td></td><td></td></tr><tr><th>NB12_Iso070</th><td>BIONOD</td><td>GER</td><td>33</td><td><i>N. brenkei</i></td><td><i>COI</i></td><td>KJ736101</td><td>ZMH K-55370</td><td>F</td></tr><tr><th>Na24</th><td>JPIO</td><td>GER PA</td><td>24</td><td><i>N. brenkei</i></td><td><i>COI</i></td><td>MT256439</td><td>ZMH K-55371</td><td>F</td></tr><tr><th>Na21</th><td>JPIO</td><td>GER PA</td><td>24</td><td><i>Nannoniscus</i> sp.</td><td><i>COI</i></td><td>MT256440</td><td>DZMB-69129</td><td>F</td></tr><tr><th>NB12_Iso099</th><td>BIONOD</td><td>FRA</td><td>67</td><td><i>N. magdae</i></td><td><i>COI</i></td><td>KJ736099</td><td>ZMH K-55373</td><td>F</td></tr><tr><th>Na12</th><td>JPIO</td><td>FRA</td><td>171</td><td><i>N. magdae</i></td><td><i>COI</i></td><td>MT256441</td><td>ZMH K-55374</td><td>F</td></tr><tr><th>Na26</th><td>JPIO</td><td>FRA</td><td>171</td><td><i>N. magdae</i></td><td><i>COI</i>,</td><td>MT256442</td><td>ZMH K-55375</td><td>F</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>16S</td><td>MT259300</td><td></td><td></td></tr><tr><th>Na28</th><td>JPIO</td><td>FRA</td><td>171</td><td><i>N. magdae</i></td><td><i>COI</i></td><td>MT256443</td><td>ZMH K-55376</td><td>F</td></tr><tr><th>Na49</th><td>JPIO</td><td>FRA</td><td>171</td><td><i>N. magdae</i></td><td><i>COI</i></td><td>MT256444</td><td>ZMH K-55377</td><td>M</td></tr><tr><th>Na19</th><td>JPIO</td><td>GER PA</td><td>20</td><td><i>Nannoniscus</i> sp.</td><td>16S</td><td>MT271781</td><td>DZMB-69130</td><td>M</td></tr><tr><th>Na33</th><td>JPIO</td><td>FRA</td><td>158</td><td><i>Nannoniscus</i> sp.</td><td>16S</td><td>MT259301</td><td>DZMB-69131</td><td>F</td></tr><tr><th>Na17</th><td>JPIO</td><td>FRA</td><td>158</td><td><i>Nannoniscus</i> sp.</td><td>16S</td><td>MT259302</td><td>DZMB-69132</td><td>F</td></tr><tr><th>NB12_Iso303</th><td>BIONOD</td><td>GER</td><td>43</td><td><i>Nannoniscus</i> sp. 4</td><td><i>COI</i></td><td>KJ736054</td><td>DZMB-69133</td><td></td></tr><tr><th>NB12_Iso310</th><td>BIONOD</td><td>GER</td><td>43</td><td><i>Nannoniscus</i> sp. 4</td><td><i>COI</i></td><td>KJ736055</td><td>DZMB-69134</td><td></td></tr><tr><th>NB12_Iso307</th><td>BIONOD</td><td>GER</td><td>43</td><td><i>Nannoniscus</i> sp. 4</td><td><i>COI</i></td><td>KJ736053</td><td>DZMB-69135</td><td></td></tr><tr><th>VTDesm013</th><td>VEMA</td><td>NEA</td><td>2–6</td><td><i>Ketosoma vemae</i></td><td><i>COI</i></td><td>MF040892</td><td>ZMH K-46140</td><td>M</td></tr><tr><th>D3D060</th><td>DIVA3</td><td>ARG</td><td>534</td><td><i>Ketosoma werneri</i></td><td><i>COI</i></td><td>MF040893</td><td>ZMH K-46142</td><td>F</td></tr><tr><th>NBIso337</th><td>BIONOD</td><td>GER</td><td>43</td><td><i>Ketosoma ruehlemanni</i></td><td><i>COI</i></td><td>KJ736158</td><td>ZMH K-46139</td><td>M</td></tr></tbody></table><p>*APEI: Area of Particular Environmental Interest, FRA: French licence area; GER: German licence area, GSR: G-TEC Sea Mineral Resources NV; OMS: Ocean Mineral Singapore Pte. Ltd.; UK: UK Seabed Resources Ltd.; IRZ: impact reference zone; PA, prospective mining area; PRZ: preservation reference zone; NEA: North-East Atlantic; Argentine basin; M: male, F: female.</p>
TABLE 2 in Ferula ermenekense (Apiaceae), an interesting new species from Southern Anatolia in the eastern Mediterraenean Basin
<p><b>TABLE 2</b> Comparison of mericarp characteristics of <i>Ferula ermenekense, F. lycia, F. duranii</i> and <i>F. pisidica</i> (L: length, W: width, T: thickness, SD: standard deviation; values in mm).</p><table><tbody><tr><th><b>Mericarpcharacters</b></th><th><i>F. ermenekense</i></th><th><i>F. lycia</i></th><th><i>F. duranii</i></th><th><i>F. pisidica</i></th></tr></tbody><tbody><tr><th>L,W</th><td>9.02–15.01mm, 5.02–7.50 mm</td><td>7.00–10.3mm, 4.00–7.01 mm</td><td>6.02–10.01 mm, 3.03–5.02 mm</td><td>8.01–14.2 mm, 5.03–8.04 mm</td></tr><tr><th>T</th><td>1.92–2.03 mm</td><td>1.25–1.50 mm</td><td>0.70–1.51 mm</td><td>1.45–2.001 mm</td></tr><tr><th>L/W</th><td>12.015/6.26:1.91</td><td>8.65/5.505:1.57</td><td>8.015/4.025:2.01</td><td>11.105/6.535:1.69</td></tr><tr><th>Mericarp Shape</th><td>obovate-eliptical</td><td>rounded-oblong</td><td>narrowly elliptical-oblong</td><td>oblong</td></tr><tr><th>Mericarp Color</th><td>brown</td><td>light brownish</td><td>dark brown</td><td>light brownish</td></tr><tr><th>Mericarp size (mm)</th><td>9–15 × 5–7,5</td><td>7–10 × 4–7</td><td>6–10 × 3–5</td><td>8–14 × 5–8</td></tr><tr><th>Mericarp wing wide (mm)</th><td>0.5–0.7</td><td>1–1.5</td><td>0.3–0.5</td><td>0.5–0.7</td></tr><tr><th>Mericarp dorsal ridges</th><td>filiform straight</td><td>slightly filiform</td><td>filiform and slightly undulate</td><td>filiform and slightly undulate</td></tr><tr><th>ornamentation</th><td>rugulose, granules</td><td>rugulose-reticulate</td><td>rugulose</td><td>rugulose-reticulate</td></tr><tr><th>Epicuticular wax</th><td>crust; sparsely irregular platelets</td><td>smooth layer; irregular and sparsely platelets</td><td>smooth layer; diffuse, dense, irregular and nonentire platelets</td><td>smooth layer; tiny and very sparsely irregular platelets</td></tr><tr><th>Epidermal cells shape</th><td>incospicous more or less isodiametric, polygonal</td><td>conspicous more or less isodiametric, especially quadrangle polygonal</td><td>inconspicous more or less isodiametric, polygonal</td><td>inconspicous rounded, more or less isodiametric</td></tr><tr><th>Anticlinal cell walls</th><td>inconspicuous, regularly thickened and straight</td><td>conspicuous, sunken, ribbed, undulate</td><td>inconspicuous, irregularly thickened and straight</td><td>inconspicuous, irregularly thickened and minutely raised to straight</td></tr><tr><th>Periclinal cells walls</th><td>flat</td><td>convex</td><td>concave</td><td>flat</td></tr></tbody></table>
Table 3 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
<p><b>Table 3.</b> Weight (in grams) and external and craniomandibular measurements (in mm) of two specimens of <i>Alpiscaptulus medogensis</i> and <i>Scapanulus oweni</i> (means ± standard deviation, observed ranges, and number of specimens)</p><table><tbody><tr><th></th><th><i>Alpiscaptulus medogensis</i></th><th><i>Scapanulus oweni</i></th></tr></tbody><tbody><tr><th></th><td>KIZ: 037966</td><td>KIZ: 037965</td><td><i>N</i> = 6</td></tr><tr><th></th><td>♀</td><td>♂</td><td></td></tr><tr><th>W</th><td>25.9</td><td>34.8</td><td>32.34 ± 7.63</td></tr><tr><td></td><td></td><td>20.50–41.80; 5</td></tr><tr><th>HB</th><td>89</td><td>111</td><td>100.83 ± 13.17</td></tr><tr><td></td><td></td><td>80.00–116.00; 6</td></tr><tr><th>TL</th><td>42</td><td>40</td><td>40.00 ± 6.51</td></tr><tr><td></td><td></td><td>33.00–49.00; 6</td></tr><tr><th>HF</th><td>18</td><td>18</td><td>16.17 ± 1.83</td></tr><tr><td></td><td></td><td>14.00–19.00; 6</td></tr><tr><th>GLS</th><td>29.08</td><td></td><td>29.59 ± 0.96</td></tr><tr><td></td><td></td><td>28.45–30.73; 4</td></tr><tr><th>BL</th><td>24.67</td><td></td><td>25.23 ± 0.65</td></tr><tr><td></td><td></td><td>24.46–26.03; 4</td></tr><tr><th>PL</th><td>12.83</td><td>12.71</td><td>13.40 ± 0.43</td></tr><tr><td></td><td></td><td>12.90–13.97; 5</td></tr><tr><th>CH</th><td>8.33</td><td></td><td>8.56 ± 0.04</td></tr><tr><td></td><td></td><td>8.52–8.60; 3</td></tr><tr><th>CB</th><td>13.41</td><td></td><td>13.77 ± 0.40</td></tr><tr><td></td><td></td><td>13.34–14.30; 4</td></tr><tr><th>IOB</th><td>6.67</td><td>6.97</td><td>6.53 ± 0.19</td></tr><tr><td></td><td></td><td>6.36–6.80; 4</td></tr><tr><th>ZB</th><td>9.85</td><td>9.5</td><td>10.77 ± 0.20</td></tr><tr><td></td><td></td><td>10.53–11.03; 4</td></tr><tr><th>UTL</th><td>12.43</td><td>11.88</td><td>12.86 ± 0.34</td></tr><tr><td></td><td></td><td>12.42–13.25; 5</td></tr><tr><th>UML</th><td>5.05</td><td>4.85</td><td>5.48 ± 0.10</td></tr><tr><td></td><td></td><td>5.41–5.62; 4</td></tr><tr><th>M2-M2</th><td>7.5</td><td>7.68</td><td>8.39 ± 0.22</td></tr><tr><td></td><td></td><td>8.12–8.73; 5</td></tr><tr><th>P4-M3</th><td>6.18</td><td>6.39</td><td>7.04 ± 0.16</td></tr><tr><td></td><td></td><td>6.95–7.28; 4</td></tr><tr><th>LTR</th><td>11.17</td><td>10.9</td><td>11.47 ± 0.30</td></tr><tr><td></td><td></td><td>11.10–11.82; 4</td></tr><tr><th>HCP</th><td>6.36</td><td>7.24</td><td>7.27 ± 0.33</td></tr><tr><td></td><td></td><td>6.88–7.67; 4</td></tr><tr><th>HCV</th><td>4.57</td><td>4.25</td><td>4.22 ± 0.20</td></tr><tr><td></td><td></td><td>3.93–4.41; 4</td></tr></tbody></table>
TABLE 1 in Preliminary account on the bryozoans of the Alboran platform (Western Mediterranean), with description of two new species
<p><b>TABLE 1.</b> List of sampling stations from the INDEmaRES- alboRaN project 2011 examined in this study.</p><table><tbody><tr><th><b>Station</b></th><th><b>Date</b></th><th><b>Position</b></th><th><b>Substrate</b></th><th><b>Depth (m)</b></th></tr></tbody><tbody><tr><th>BV12</th><td>23/09/2011</td><td>35°52.22’N – 03°05.21’W, 35°52.17’N – 03°05.38’W</td><td>Gravel</td><td>112–120</td></tr><tr><th>BV13</th><td>23/09/2011</td><td>35°52.38’N – 03°05.18’W, 35°52.82’N – 03°04.59’W</td><td>Gravel</td><td>95–99</td></tr><tr><th>BV14</th><td>23/09/2011</td><td>35°52.72’N – 03°04.67’W, 35°52.34’N – 03°05.26’W</td><td>Gravel</td><td>96–100</td></tr><tr><th>BV15</th><td>23/09/2011</td><td>35°52.67’N – 03°04.66’W, 35°52.90’N – 03°04.92’W</td><td>Gravel</td><td>96</td></tr></tbody></table>
Table 1 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
<p><b>Table 1.</b> Station list of CCZ sampling sites across where examined <i>Nannoniscus</i> specimens were collected [including gear type, date, position (degrees) and depth (m)]</p><table><tbody><tr><th>Voyage</th><th>Area</th><th>Gear</th><th>Station</th><th>Date</th><th>Start latitude °N</th><th>Start longitude °W</th><th>End latitude °N</th><th>End longitude °W</th><th>Depth (m)</th></tr></tbody><tbody><tr><th>AB02</th><td>OMS*</td><td>EBS</td><td>S10</td><td>2015-03-14</td><td>12°2’17.16’’</td><td>117°14’12’’</td><td>12°2’29’’</td><td>117°13’1’’</td><td>4097–4094</td></tr><tr><th>AB02</th><td>OMS</td><td>EBS</td><td>S11</td><td>2015-03-16</td><td>12°2’43.08’’</td><td>117°25’26’’</td><td>12°3’1.44’’</td><td>117°24’17’’</td><td>4223–4235</td></tr><tr><th>AB02</th><td>APEI-6</td><td>EBS</td><td>APEI-6#1</td><td>2015-03-20</td><td>19°27’52’’</td><td>120°1’31’’</td><td>19°28’54’’</td><td>120°0’58’’</td><td>4099–4076</td></tr><tr><th>AB02</th><td>OMS</td><td>EBS</td><td>S5</td><td>2015-03-01</td><td>12°15’3’’</td><td>117°19’14’’</td><td>n.a.</td><td>n.a.</td><td>4137</td></tr><tr><th>AB02</th><td>UK</td><td>EBS</td><td>U7</td><td>2015-03-02</td><td>12°27’5’’</td><td>116°37’48’’</td><td>n.a.</td><td>n.a.</td><td>4145</td></tr><tr><th>JPIO</th><td>GER PA</td><td>EBS</td><td>20</td><td>2015-03-21</td><td>11°50’9’’</td><td>117°58’29’’</td><td>11°50’11’’</td><td>116°58’0’’</td><td>4093</td></tr><tr><th>JPIO</th><td>GER PA</td><td>EBS</td><td>24</td><td>2015-03-22</td><td>11°51’19’’</td><td>117°1’30’’</td><td>11°51’31’’</td><td>116°58’0’’</td><td>4093</td></tr><tr><th>JPIO</th><td>GSR</td><td>EBS</td><td>117</td><td>2015-04-07</td><td>13°52’19’’</td><td>123°15’27’’</td><td>13°52’37’’</td><td>123°14’16’’</td><td>4498–4521</td></tr><tr><th>JPIO</th><td>GSR</td><td>EBS</td><td>133</td><td>2015-04-10</td><td>13°50’45’’</td><td>123°15’39’’</td><td>13°51’8’’</td><td>123°14’8’’</td><td>4516–4427</td></tr><tr><th>JPIO</th><td>FRA</td><td>EBS</td><td>158</td><td>2015-04-15</td><td>14°3’25’’</td><td>130°7’59’’</td><td>14°3’49’’</td><td>130°6’29’’</td><td>4946–4978</td></tr><tr><th>JPIO</th><td>FRA</td><td>EBS</td><td>171</td><td>2015-04-17</td><td>14°2’41’’</td><td>130°5’57’’</td><td>14°3’12’’</td><td>130°4’36’’</td><td>5024–5017</td></tr><tr><th>MA13</th><td>GER PA</td><td>EBS</td><td>07</td><td>2013-04-12</td><td>11°51’30.18’’</td><td>117°01’12.30’’</td><td>11°51’45.36’’</td><td>117°0’10.26’’</td><td>4131–4121</td></tr><tr><th>MA13</th><td>GER PRZ</td><td>EBS</td><td>90</td><td>2013-05-03</td><td>11°49’44.52’’</td><td>117°30’16.68’’</td><td>111°49’54.36’’</td><td>117°29’23.7’’</td><td>4340–4357</td></tr><tr><th>MA14</th><td>GER IRZ</td><td>EBS</td><td>20</td><td>2014-05-10</td><td>11°51’32’’</td><td>117°01’8’’</td><td>11°51’43’’</td><td>117°00’19’’</td><td>4127–4124</td></tr><tr><th>MA14</th><td>GER IRZ</td><td>EBS</td><td>21</td><td>2014-05-10</td><td>11°49’44.52’’</td><td>117°00’27.06’’</td><td>11°49’56.76’’</td><td>116°59’40.62’’</td><td>4132–4136</td></tr><tr><th>MA14</th><td>GER PRZ</td><td>EBS</td><td>38</td><td>2014-05-13</td><td>11°47’52’’</td><td>117°30’31’’</td><td>11°48’3’’</td><td>117°29’45’’</td><td>4363–4373</td></tr><tr><th>MA14</th><td>GER PRZ</td><td>EBS</td><td>39</td><td>2014-05-13</td><td>11°49’37’’</td><td>117°30’49’’</td><td>11°49’47’’</td><td>117°30’5’’</td><td>4361–4343</td></tr><tr><th>BIONOD</th><td>GER</td><td>EBS</td><td>06</td><td>2012-04-02</td><td>11°46’13’’</td><td>116°41’8’’</td><td>11°46’13’’</td><td>116°41’7’’</td><td>4259</td></tr><tr><th>BIONOD</th><td>GER</td><td>EBS</td><td>33</td><td>2012-04-07</td><td>11°51’44’’</td><td>117°3’10’’</td><td>11°51’54’’</td><td>117°3’8’’</td><td>4133</td></tr><tr><th>BIONOD</th><td>GER</td><td>EBS</td><td>43</td><td>2012-04-09</td><td>11°48’12’’</td><td>117°32’3’’</td><td>11°48’20’’</td><td>117°31’57.079’’</td><td>4358</td></tr><tr><th>BIONOD</th><td>FRA</td><td>EBS</td><td>67</td><td>2012-04-19</td><td>14°3’4’’</td><td>130°4’36’’</td><td>14°3’10’’</td><td>130°4’27’’</td><td>5021</td></tr><tr><th>BIONOD</th><td>FRA</td><td>EBS</td><td>101</td><td>2012-04-25</td><td>14°4’51’’</td><td>130° 6’11’’</td><td>14°5’0’’</td><td>130°6’11’’</td><td>5055</td></tr></tbody></table><p>*APEI: Area of Particular Environmental Interest; FRA: French licence area; GER: German licence area; GSR: G-TEC Sea Mineral Resources NV; OMS: Ocean Mineral Singapore Pte. Ltd.; UK: UK Seabed Resources Ltd.; IRZ: impact reference zone; PA, prospective mining area; PRZ: preservation reference zone.</p>
Table 4. The K 2 P in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
<p><b>Table 4.</b> The K2P distance of the <i>CYT B</i> gene in the genera of the Scalopini</p><table><tbody><tr><th><i>Alpiscaptulus Parascalops Scapanulus Scapanus</i></th></tr><tr><th><i>Alpiscaptulus</i></th></tr></tbody><tbody><tr><th><i>Parascalops</i></th><td>0.145</td><td></td><td></td><td></td></tr><tr><th><i>Scapanulus</i></th><td>0.161</td><td>0.171</td><td></td><td></td></tr><tr><th><i>Scapanus</i></th><td>0.174</td><td>0.156</td><td>0.189</td><td></td></tr><tr><th><i>Scalopus</i></th><td>0.189</td><td>0.186</td><td>0.217</td><td>0.172</td></tr></tbody></table>
TABLE 1 in Connecting the dots: DNA barcoding and lectotype designation shedding light on Labrundinia longipalpis (Goetghebuer, 1921), an intriguing non-biting midge (Chironomidae, Tanypodinae)
<p><b>TABLE 1.</b> List of analyzed specimens, including their sample localities, life stage, and voucher reference and GenBank accession numbers.</p><table><tbody><tr><th><b>Taxon</b></th><th><b>Country</b></th><th><b>Stage</b></th><th><b>Voucher number</b></th><th><b>Accession number</b></th></tr></tbody><tbody><tr><th><i>Labrundinia amandae</i></th><td>Brazil</td><td>Immature</td><td>NEOTA044-12</td><td>JX887502.1</td></tr><tr><th><i>Labrundinia fiorelinii</i></th><td>Brazil</td><td>Immature</td><td>MPCB005-09</td><td>HM379514.1</td></tr><tr><th><i>Labrundinia jasoni</i></th><td>Brazil</td><td>Immature</td><td>NEOTA059-12</td><td>JX887518.1</td></tr><tr><th><i>Labrundinia longipalpis</i></th><td>Finland</td><td>Adult</td><td>ZMUO.025300</td><td>MZ660598.1</td></tr><tr><th><i>Labrundinia longipalpis</i></th><td>Finland</td><td>Adult</td><td>ZMUO.025299</td><td>MZ658837.1</td></tr><tr><th><i>Labrundinia maculata</i></th><td>USA</td><td>Immature</td><td>CATP8. 8</td><td>MW283530.1</td></tr><tr><th><i>Labrundinia mayaca</i></th><td>Brazil</td><td>Immature</td><td>NEOTA029-12</td><td>JX887525.1</td></tr><tr><th><i>Labrundinia parafittkaui</i></th><td>Brazil</td><td>Adult</td><td>NEOTA073-12</td><td>JX887508.1</td></tr><tr><th><i>Labrundinia parareniformis</i></th><td>Brazil</td><td>Immature</td><td>NEOTA035-12</td><td>JX887496.1</td></tr><tr><th><i>Labrundinia paravirescens</i></th><td>Brazil</td><td>Adult</td><td>NEOTA041-12</td><td>JX887527.1</td></tr><tr><th><i>Labrundinia reniformis</i></th><td>Brazil</td><td>Adult</td><td>NEOTA033-12</td><td>JX887489.1</td></tr><tr><th><i>Labrundinia sofiae</i></th><td>Brazil</td><td>Adult</td><td>NEOTA076-12</td><td>JX887517.1</td></tr></tbody></table>
TABLE 1. A in Ferula ermenekense (Apiaceae), an interesting new species from Southern Anatolia in the eastern Mediterraenean Basin
<p><b>TABLE 1.</b> A comparison of selected characters differing among <i>F. ermenekense, F. lycia, F. duranii</i> and <i>F. pisidica</i>.</p><table><tbody><tr><th><b>Characters</b></th><th><i>Ferula ermenekense</i></th><th><i>F. lycia</i></th><th><i>F. duranii</i></th><th><i>F. pisidica</i></th></tr></tbody><tbody><tr><th>Basal leaves</th><td>4–5(–6) pinnate</td><td>6 pinnate</td><td>6–7 pinnate</td><td>6–7 pinnate</td></tr><tr><th>Basal leaves</th><td>sparsely scabrid</td><td>glabrous</td><td>glabrous</td><td>setulose</td></tr><tr><th>Ultimate segments</th><td>linear, 4–10 (–12) × 1–3 mm</td><td>oblong-linear, 1–2 × 0.5–1 mm</td><td>linear, 3–8 × 0.4–0.8 mm</td><td>linear, 1–4 × 0.5–1.5 mm</td></tr><tr><th>Ultimate segments apex</th><td>acuminate</td><td>acute</td><td>acuminate</td><td>obtuse</td></tr><tr><th>Inflorescence</th><td>dense</td><td>lax</td><td>lax</td><td>lax</td></tr><tr><th>Sheaths</th><td>lanceolate</td><td>ovate</td><td>lanceolate</td><td>ovate</td></tr><tr><th>Upper sheaths lamina</th><td>very reduced</td><td>very reduced</td><td>distinctly leafy</td><td>very reduced</td></tr><tr><th>Central umbels rays</th><td>14–26</td><td>6–16</td><td>14–22</td><td>8–22</td></tr><tr><th>Central umbels pedicel</th><td>7–10 mm</td><td>6–14</td><td>5–10 mm</td><td>2–8 mm</td></tr><tr><th>Umbellules flowers</th><td>(10–)15–23</td><td>10–15</td><td>20–40</td><td>9–15</td></tr><tr><th>Petals</th><td>glabrous</td><td>glabrous</td><td>glabrous</td><td>setulose</td></tr><tr><th>Mericarps</th><td>obovate-elliptic, 9–15 × 5–7.5 mm</td><td>orbicular-oblong, 7–10 × 4–7 mm</td><td>narrowly elliptic-blong, 6–10 × 3–5 mm</td><td>oblong, 8–14 × 4–9 mm</td></tr><tr><th>Dorsal vittae per vallecula</th><td>1–2</td><td>1</td><td>2–3</td><td>1–3</td></tr><tr><th>Commussural vittae</th><td>6–8</td><td>2–4</td><td>4–6</td><td>(2–)4–6</td></tr><tr><th>Lateral wings wide</th><td>0.5–0.7 mm</td><td>1–1.5 mm</td><td>0.3–0.5 mm</td><td>0.5–1 mm</td></tr></tbody></table>
Table 1 in Molecular analysis reveals a cryptic species of Chthamalus (Crustacea: Cirripedia) in the Cape Verde Islands
<p><b>Table 1.</b> Number of individuals for each marker</p><table><tbody><tr><th><i>Chthamalus</i> species</th><th><i>EF1</i></th><th><i>NaKA</i></th><th><i>COI</i></th></tr></tbody><tbody><tr><th><i>C. alani</i></th><td>24</td><td>8</td><td>19</td></tr><tr><th><i>C. angustitergus</i></th><td>18</td><td>7</td><td>23</td></tr><tr><th><i>C. dalli</i></th><td>8</td><td>8</td><td>164</td></tr><tr><th><i>C. fissus</i></th><td>10</td><td>6</td><td>12</td></tr><tr><th><i>C. hedgecocki</i></th><td>10</td><td>8</td><td>9</td></tr><tr><th><i>C. panamensis</i></th><td>19</td><td>9</td><td>33</td></tr><tr><th><i>C. proteus</i></th><td>16</td><td>9</td><td>22</td></tr><tr><th><i>C. stellatus</i></th><td>236</td><td>233</td><td>61</td></tr><tr><th>Cape Verde population</th><td>37</td><td>37</td><td>12</td></tr><tr><th>Total</th><td>378</td><td>325</td><td>355</td></tr></tbody></table>
Table 2 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
<p><b>Table 2.</b> Samples and sequences used for molecular analyses, new sequences generated in this study are shown in bold</p><table><tbody><tr><th>Species</th><th>Museum code</th><th>Sample locality</th><th><i>CYT B</i></th><th>12S</th><th><i>APOB</i></th><th><i>BRCA1</i></th><th><i>RAG2</i></th></tr></tbody><tbody><tr><th><i>Alpiscaptulus</i> <i>medogensis</i></th><td>KIZ: 037965</td><td>China: Tibet</td><td><b>MT349295</b></td><td><b>MT349878</b></td><td><b>MT349297</b></td><td><b>MT349299</b></td><td><b>MT349301</b></td></tr><tr><th><i>Alpiscaptulus</i> <i>medogensis</i></th><td>KIZ: 037966</td><td>China: Tibet</td><td><b>MT349296</b></td><td><b>MT349879</b></td><td><b>MT349298</b></td><td><b>MT349300</b></td><td><b>MT349302</b></td></tr><tr><th><i>Scapanulus oweni</i></th><td>KIZ: 036922</td><td>China: Gansu</td><td>KX754480</td><td>KX754509</td><td>KX755181</td><td>KX754542</td><td>KX754602</td></tr><tr><th><i>Scapanulus oweni</i></th><td>KIZ: 037964</td><td>China: Gansu</td><td>KX754481</td><td>KX754510</td><td>KX755182</td><td>KX754543</td><td>KX754603</td></tr><tr><th><i>Scapanulus oweni</i></th><td>KIZ: 036923</td><td>China: Gansu</td><td>KX754482</td><td>KX754511</td><td>KX755183</td><td>KX754544</td><td>KX754604</td></tr><tr><th><i>Scapanulus oweni</i></th><td>KIZ: 027013</td><td>China: Shaanxi</td><td>KX754483</td><td>KX754512</td><td>KX755184</td><td>KX754545</td><td>KX754605</td></tr><tr><th><i>Parascalops breweri</i></th><td>HT-1</td><td>USA: New York</td><td>AB076808</td><td>KX754496</td><td>KX755167</td><td>KX754529</td><td>KX754589</td></tr><tr><th><i>Scapanus latimanus</i></th><td>BF-1</td><td>USA: California</td><td>AB076813</td><td>KX754497</td><td>KX755170</td><td>KX754532</td><td>KX754592</td></tr><tr><th><i>Scapanus orarius</i></th><td>UWBM:81154</td><td>USA: Oregon</td><td>KX754472</td><td>KX754500</td><td>KX755171</td><td>KX754533</td><td>KX754593</td></tr><tr><th><i>Scapanus orarius</i></th><td>UWBM:81163</td><td>USA: California</td><td>KX754473</td><td>—</td><td>KX755172</td><td>KX754534</td><td>KX754594</td></tr><tr><th><i>Scapanus orarius</i></th><td>CM-3</td><td>Canada: British Columbia</td><td>AB076816</td><td>KX754501</td><td>KX755173</td><td>—</td><td>—</td></tr><tr><th><i>Scapanus townsendii</i></th><td>UWBM:81168</td><td>USA: Washington</td><td>KX754474</td><td>KX754502</td><td>KX755174</td><td>KX754535</td><td>KX754595</td></tr><tr><th><i>Scapanus townsendii</i></th><td>TM-3</td><td>USA: Washington</td><td>AB076820</td><td>KX754503</td><td>KX755175</td><td>KX754536</td><td>KX754596</td></tr><tr><th><i>Scalopus aquaticus</i></th><td>HPW622</td><td>USA: Illinois</td><td>KX754471</td><td>KX754498</td><td>KX755169</td><td>KX754531</td><td>KX754591</td></tr><tr><th><i>Scalopus aquaticus</i></th><td>NMMNH:DJH4822:4348</td><td>USA: Iowa</td><td>KX754470</td><td>KX754497</td><td>KX755168</td><td>KX754530</td><td>KX754590</td></tr><tr><th><i>Euroscaptor</i> <i>longirostris</i></th><td>KIZ: 0905172</td><td>China: Sichuan</td><td>HG737870</td><td>HG737884</td><td>KX755148</td><td>HG737899</td><td>HG737932</td></tr><tr><th><i>Euroscaptor</i> <i>longirostris</i></th><td>KIZ: 0905290</td><td>China: Sichuan</td><td>HG737871</td><td>HG737885</td><td>KX755149</td><td>HG737900</td><td>HG737933</td></tr><tr><th><i>Euroscaptor parvidens</i></th><td>SIK:0859</td><td>Viet Nam: Quang Nam</td><td>AB823121</td><td>AB823156</td><td>KX755147</td><td>KX754521</td><td>HG737931</td></tr><tr><th><i>Scaptonyx fusicaudus</i></th><td>KIZ: GLGS5532</td><td>China: Yunnan</td><td>KX754475</td><td>KX754504</td><td>KX755177</td><td>KX754537</td><td>KX754597</td></tr><tr><th><i>Scaptonyx fusicaudus</i></th><td>KIZ: GLGS5974</td><td>China: Yunnan</td><td>KX754476</td><td>KX754505</td><td>KX755178</td><td>KX754538</td><td>KX754598</td></tr><tr><th><i>Parascaptor leucura</i></th><td>KIZ: DY0054</td><td>China: Yunnan</td><td>HG737877</td><td>HG737891</td><td>KX755161</td><td>HG737905</td><td>HG737939</td></tr><tr><th><i>Parascaptor leucura</i></th><td>KIZ: 0412179</td><td>China: Yunnan</td><td>HG737878</td><td>HG737892</td><td>KX755162</td><td>HG737906</td><td>HG737940</td></tr><tr><th><i>Episoriculus caudatus</i></th><td>THUB-S-00005</td><td>China: Taiwan</td><td>GU981272</td><td>GU981030</td><td>GU981118</td><td>GU981193</td><td>GU981451</td></tr><tr><th><i>Uropsilus nivatus</i></th><td>KIZ: 0705081</td><td>China: Yunnan</td><td>KX754484</td><td>KX754513</td><td>KX755187</td><td>KX754546</td><td>KX754606</td></tr></tbody></table>
TABLE 1 in A new species of Batillipes (Arthrotardigrada: Batillipedidae) from the mid littoral zone of the southeast coast of India
<p><b>TABLE 1.</b> Morphometrics (μm) of <i>Batillipes kalami</i> <b>sp. nov.</b>, <i>n</i>, number of specimens observed.</p><table><tbody><tr><th><b>Characters</b></th><th><b>Holotype</b> female</th><th><b>Paratypes average females, <i>n</i> =5</b></th><th><b>Paratypes average males, <i>n</i> =4</b></th></tr></tbody><tbody><tr><th><b>Voucher No.</b></th><td>VD9</td><td>VD10, 11, 13, 15, 18</td><td>VD12, 14, 16, 17</td></tr><tr><th>Body length</th><td>170.2</td><td>164.2 ± 4.9</td><td>162.5 ± 5.1</td></tr><tr><th>Body width</th><td>51.5</td><td>49.5 ± 2.8</td><td>49.8 ± 2.7</td></tr><tr><th>Cephalic region width</th><td>45.4</td><td>44.9 ± 2.1</td><td>45.2 ± 2.3</td></tr><tr><th>Median cirrus</th><td>9.8</td><td>9.7 ± 0.7</td><td>9.8 ± 0.9</td></tr><tr><th>Internal cirri</th><td>12.7</td><td>12.5 ± 1.2</td><td>12.2 ± 0.9</td></tr><tr><th>External cirri</th><td>12.1</td><td>11.8 ± 1.5</td><td>11.9 ± 1.2</td></tr><tr><th>Lateral cirri</th><td>29.3</td><td>27.9 ± 0.9</td><td>28.0 ± 1.1</td></tr><tr><th>Primary clavae</th><td>11.7</td><td>10.9 ± 0.9</td><td>11.4 ± 1.0</td></tr><tr><th>Cirri E</th><td>22.5</td><td>20.9 ± 1.5</td><td>21.9 ± 1.2</td></tr><tr><th>Caudal apparatus</th><td>23.4</td><td>22.5 ± 3.9</td><td>22.8 ± 4.2</td></tr><tr><th>Body projection 1</th><td>9.9</td><td>9.6 ± 1.1</td><td>9.6 ± 1.0</td></tr><tr><th>Body projection 2</th><td>9.4</td><td>9.2 ± 1.5</td><td>9.2 ± 1.3</td></tr><tr><th>Body projection 3</th><td>11.5</td><td>11.6 ± 1.3</td><td>11.8 ± 1.4</td></tr><tr><th>Body projection 4</th><td>9.7</td><td>9.6 ± 0.8</td><td>9.5 ± 1.0</td></tr><tr><th>Body projection 5</th><td>18.4</td><td>18.2 ± 1.4</td><td>18.7 ± 2.0</td></tr><tr><th>Leg I–III: Toe 1</th><td>8.7</td><td>7.9 ± 0.9</td><td>8.0 ± 1.0</td></tr><tr><th>Toe 2</th><td>6.1</td><td>6.1 ± 0.7</td><td>6.6 ± 0.8</td></tr><tr><th>Toe 3</th><td>11.2</td><td>10.8 ± 0.8</td><td>11.7 ± 0.9</td></tr><tr><th>Toe 4</th><td>6</td><td>5.9 ± 0.4</td><td>6.0 ± 0.6</td></tr><tr><th>Toe 5</th><td>17.1</td><td>15.5 ± 1.0</td><td>16.1 ± 1.0</td></tr><tr><th>Toe 6</th><td>11.8</td><td>10.1 ± 0.9</td><td>9.4 ± 1</td></tr><tr><th>Leg IV: Toe 1</th><td>7.4</td><td>7.6 ± 1.0</td><td>7.7 ± 1.1</td></tr><tr><th>Toe 2</th><td>11.9</td><td>11.7 ± 1.1</td><td>12.1 ± 0.7</td></tr><tr><th>Toe 3</th><td>5.6</td><td>5.9 ± 0.9</td><td>6.1 ± 1.0</td></tr><tr><th>Toe 4</th><td>5.5</td><td>5.6 ± 1.0</td><td>5.4 ± 0.8</td></tr><tr><th>Toe 5</th><td>12.9</td><td>13.0 ± 1.2</td><td>12.2 ± 1.0</td></tr><tr><th>Toe 6</th><td>7.3</td><td>7.3 ± 0.8</td><td>7.4 ± 0.9</td></tr><tr><th>Leg I spine</th><td>9.5</td><td>10.0 ± 1.6</td><td>9.9 ± 1.0</td></tr><tr><th>Leg II spine</th><td>12.8</td><td>12.7 ± 2.1</td><td>12.5 ± 1.8</td></tr><tr><th>Leg III spine</th><td>10.1</td><td>11.2 ± 1.4</td><td>11.9 ± 1.3</td></tr><tr><th>Leg IV sense organ</th><td>11.7</td><td>11.3 ± 1.8</td><td>12.1 ± 1.9</td></tr></tbody></table>
Table 2 in Two new related oodine genera in the Oriental Region, with remarks on the systematic position of the genera Hololeius and Holosoma (Coleoptera, Carabidae)
<p>Table 2. Diagnostic character state combinations shown by exemplars of Hololeius ceylanicus and Hololeius cyaneus.</p><table><tbody><tr><th>No.</th><th>Characters</th><th>Hololeius ceylanicus</th><th>Hololeius cyaneus</th></tr></tbody><tbody><tr><td>01</td><td>Pubescence of integument</td><td>partly pubescent</td><td>glabrous</td></tr><tr><td>02</td><td>Punctuation of integument</td><td>punctate (Figs 1-3)</td><td>impunctate (Figs 13-16)</td></tr><tr><td>03</td><td>Antennomere 3</td><td>with a few short and scattered setae</td><td>glabrous</td></tr><tr><td>04</td><td>Mentum tooth form anteriorly</td><td>truncate</td><td>rounded</td></tr><tr><td>05</td><td>PW/PL</td><td>1.14-1.15 (Fig. 1)</td><td>1.24-1.37 (Fig. 13)</td></tr><tr><td>06</td><td>Basal margin of pronotum at posterior angles</td><td>oblique (Fig. 1)</td><td>gradually rounded (Fig. 13)</td></tr><tr><td>07</td><td>Pronotum</td><td>bordered laterally and lateroapically, not bordered medioapically and basally (Fig. 1)</td><td>bordered throughout (Fig. 13)</td></tr><tr><td>08</td><td>Elytral striae 1-8</td><td>1-7 punctate, 8 impunctate (Fig. 2)</td><td>impunctate (Fig. 14)</td></tr><tr><td>09</td><td>Stria 8</td><td>not or hardly deeper than other striae (Figs 2-3)</td><td>evidently deeper than other striae (Figs 14-16)</td></tr><tr><td>10</td><td>Elytral intervals</td><td>punctate (Figs 2-3)</td><td>impunctate (Figs 14-16)</td></tr><tr><td>11</td><td>Interval 9</td><td>distinct throughout</td><td>transformed into marginal gutter along anterior 2/5 of elytra, distinct in posterior 3/5</td></tr><tr><td>12</td><td>Number of umbilicate pores</td><td>23-25</td><td>15-16</td></tr><tr><td>13</td><td>Mesocoxa lateral margin</td><td>with one long seta</td><td>without seta</td></tr><tr><td>14</td><td>Joins of claws</td><td>opposite, distantly situated from each other</td><td>nearly parallel, closely situated to each other (Figs 14-15)</td></tr><tr><td>15</td><td>Number of pores on last sternum in female</td><td>four pores</td><td>two pores</td></tr><tr><td>16</td><td>Apical stylomere of ovipositor</td><td>subtriangular, as wide as basal stylomere, with 36 long ensiform setae at dorsomedial, dorsolateral and ventral position, and with nematiform setae, shorter than ensiform setae (Figs 10-11)</td><td>subelongate, nearly twice as narrow as basal stylomere, with 11 short ensiform setae at dorsomedial and dorsolateral position, and with nematiform setae, nearly twice as long as ensiform setae (Figs 17-18)</td></tr></tbody></table>
Table 1 in Two new related oodine genera in the Oriental Region, with remarks on the systematic position of the genera Hololeius and Holosoma (Coleoptera, Carabidae)
<p>Table 1. List of the Oriental genera of Oodini, their species number and distribution.</p><table><tbody><tr><th>Genera</th><th>Species</th><th>Distribution (incl. unpublished data)</th></tr></tbody><tbody><tr><td>Anatrichis LeConte, 1853</td><td>3</td><td>Indian subcontinent, Myanmar, Philippines</td></tr><tr><td>Bamaroodes B. Guéorguiev, gen. n.</td><td>1</td><td>Myanmar, Thailand</td></tr><tr><td>Brachyodes Jeannel, 1949</td><td>4</td><td>whole region</td></tr><tr><td>Holcocoleus Chaudoir in Oberthur, 1883</td><td>2</td><td>India (Tamil Nadu), Ceylon</td></tr><tr><td>" Holosoma boettcheri Jedlička, 1936 "</td><td>1</td><td>Philippines</td></tr><tr><td>Megaloodes Lesne, 1896</td><td>1</td><td>SE Thailand, E Cambodia</td></tr><tr><td>Miltodes Andrewes, 1922</td><td>1</td><td>India, Thailand, Sumatra</td></tr><tr><td>Nanodiodes Bousquet, 1996</td><td>3</td><td>Ceylon, SE Asia, Indonesia, Philippines</td></tr><tr><td>Oodes Bonelli, 1810</td><td>16</td><td>whole region</td></tr><tr><td>Oodinus Motschulsky, 1864</td><td>1</td><td>Vietnam, Sumatra, Moluccas, Philippines</td></tr><tr><td>Pseudosphaerodes Jeannel, 1949</td><td>2</td><td>Myanmar, Philippines</td></tr><tr><td>Simous Chaudoir, 1882</td><td>9</td><td>whole region east of Bengal</td></tr><tr><td>Systolocranius Chaudoir, 1857</td><td>1</td><td>“Bengal”: MNHUB; "Ind. or.": NMW</td></tr><tr><td>Thaioodes B. Guéorguiev, gen. n.</td><td>1</td><td>Thailand</td></tr></tbody></table>
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