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TABLE 2 in Early Cretaceous angiosperm leaves from the Dakota Formation, Hoisington III locality, Kansas, USA
<p><b>TABLE 2.</b> Comparisons of leaf shape and venation of <i>Rogersia</i> and <i>Wolfiophyllum</i> species (modified from table 1 of Wang and Dilcher, 2009).</p><table><tbody><tr><th></th><th></th><th><b>Number of 2º</b></th><th><b>Loops near</b></th><th><b>Intercostal</b></th><th><b>Intersecondary</b></th><th><b>Tertiary</b></th></tr></tbody><tbody><tr><th><b>Taxon</b></th><td><b>Leaf shape</b></td><td><b>2º venation</b></td><td><b>veins</b></td><td><b>margin</b></td><td><b>region</b></td><td><b>veins</b></td><td><b>veins</b></td></tr><tr><th><i>Wolfiophyllum pfaffianum</i></th><td>very narrow elliptic</td><td>eucamptodromous</td><td>8</td><td>no</td><td>no</td><td>common</td><td>reticulate</td></tr><tr><th><i>Wolfiophyllum heigii</i></th><td>lorate or linear</td><td>eucamptodromous</td><td>10 to 12</td><td>no</td><td>no</td><td>present</td><td>percurrent or exmedially ramified</td></tr><tr><th><i>Wolfiophyllum daphneoides</i></th><td>narrow ovate to lanceolate</td><td>eucamptodromous</td><td>5 to 7</td><td>no</td><td>no</td><td>common, simple</td><td>Not observed</td></tr><tr><th><i>Rogersia dakotensis</i></th><td>linear oblong</td><td>brochidodromous</td><td>>10</td><td>two series, elongate area</td><td>well defined</td><td>present</td><td>percurrent, more or less irregular</td></tr><tr><th><i>Rogersia lottii</i></th><td>narrow elliptic</td><td>festooned brochidodromous</td><td>10</td><td>one series</td><td>well defined</td><td>present, simple</td><td>random reticulate</td></tr><tr><th><i>Rogersia parlatorii</i></th><td>oblong, lorate to linear</td><td>brochidodromous</td><td>>10</td><td>irregular</td><td>elongate and admedially oriented</td><td>common</td><td>intergrading with 2º and 4º</td></tr></tbody></table>
Table 12 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
<p><b>Table 12.</b> Length of appendage-segments in millimeters in <i>Nemastoma bidentatum sneznikensis</i> ssp. nov. from Mt. Snežnik, Slovenia: ♂ holotype (♀).</p><table><tbody><tr><th></th><th><b>Trochanter</b></th><th><b>Femur</b></th><th><b>Patella</b></th><th><b>Tibia</b></th><th><b>Metatarsus</b></th><th><b>Tarsus</b></th><th><b>Total length</b></th></tr></tbody><tbody><tr><th><b>Pedipalp</b></th><td>0.20 (0.15)</td><td>0.59 (0.58)</td><td>0.43 (0.48)</td><td>0.33 (0.38)</td><td>–</td><td>0.24 (0.25)</td><td>1.79 (1.84)</td></tr><tr><th><b>Leg I</b></th><td>0.19 (0.18)</td><td>0.73 (0.62)</td><td>0.31 (0.28)</td><td>0.52 (0.51)</td><td>0.79 (0.96)</td><td>0.74 (0.63)</td><td>3.28 (3.18)</td></tr><tr><th><b>Leg II</b></th><td>0.19 (0.23)</td><td>1.16 (0.95)</td><td>0.38 (0.38)</td><td>1.03 (0.93)</td><td>1.46 (1.61)</td><td>1.27 (1.24)</td><td>5.49 (5.34)</td></tr><tr><th><b>Leg III</b></th><td>0.18 (0.17)</td><td>0.70 (0.78)</td><td>0.29 (0.27)</td><td>0.53 (0.52)</td><td>0.86 (1.04)</td><td>0.63 (0.57)</td><td>3.19 (3.35)</td></tr><tr><th><b>Leg IV</b></th><td>0.17 (0.18)</td><td>1.06 (0.98)</td><td>0.33 (0.28)</td><td>0.74 (0.73)</td><td>1.42 (1.44)</td><td>1.01 (0.92)</td><td>4.73 (4.53)</td></tr></tbody></table>
Table 9 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
<p><b>Table 9.</b> Length of appendage-segments in millimeters in <i>N. kozari</i> Novak, Kozel, Podlesnik & Raspotnig sp. nov. from Vlašić planina, Bosnia and Herzegovina: ♂ holotype (♀).</p><table><tbody><tr><th></th><th><b>Trochanter</b></th><th><b>Femur</b></th><th><b>Patella</b></th><th><b>Tibia</b></th><th><b>Metatarsus</b></th><th><b>Tarsus</b></th><th><b>Total length</b></th></tr></tbody><tbody><tr><th><b>Pedipalp</b></th><td>0.25 (0.28)</td><td>0.74 (0.69)</td><td>0.51 (0.55)</td><td>0.41 (0.43)</td><td>–</td><td>0.28 (0.29)</td><td>2.19 (2.24)</td></tr><tr><th><b>Leg I</b></th><td>0.22 (0.23)</td><td>0.87 (0.76)</td><td>0.35 (0.30)</td><td>0.59 (0.62)</td><td>0.97 (0.91)</td><td>0.82 (0.88)</td><td>3.82 (3.70)</td></tr><tr><th><b>Leg II</b></th><td>0.24 (0.24)</td><td>1.32 (1.22)</td><td>0.44 (0.36)</td><td>1.08 (1.00)</td><td>1.87 (1.72)</td><td>1.46 (1.37)</td><td>6.41 (5.91)</td></tr><tr><th><b>Leg III</b></th><td>0.23 (0.26)</td><td>0.82 (0.78)</td><td>0.33 (0.31)</td><td>0.53 (0.51)</td><td>1.09 (1.06)</td><td>0.82 (0.72)</td><td>3.82 (3.64)</td></tr><tr><th><b>Leg IV</b></th><td>0.27 (0.26)</td><td>1.28 (1.23)</td><td>0.43 (0.38)</td><td>0.88 (0.77)</td><td>1.74 (1.69)</td><td>1.04 (0.79)</td><td>5.64 (5.12)</td></tr></tbody></table>
Table 10 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
<p><b>Table 10.</b> Length of appendage-segments in millimeters in <i>N. bidentatum martensi</i> Novak, Slana Novak & Raspotnig ssp. nov. from Poljane pri Podgradu, Slovenia: ♂ holotype (♀).</p><table><tbody><tr><th></th><th><b>Trochanter</b></th><th><b>Femur</b></th><th><b>Patella</b></th><th><b>Tibia</b></th><th><b>Metatarsus</b></th><th><b>Tarsus</b></th><th><b>Total length</b></th></tr></tbody><tbody><tr><th><b>Pedipalp</b></th><td>0.27 (0.26)</td><td>0.73 (0.76)</td><td>0.48 (0.55)</td><td>0.44 (0.47)</td><td>–</td><td>0.27 (0.29)</td><td>2.19 (2.33)</td></tr><tr><th><b>Leg I</b></th><td>0.23 (0.23)</td><td>0.93 (0.80)</td><td>0.35 (0.35)</td><td>0.60 (0.56)</td><td>1.03 (0.94)</td><td>0.78 (0.89)</td><td>3.92 (3.88)</td></tr><tr><th><b>Leg II</b></th><td>0.22 (0.23)</td><td>1.43 (1.35)</td><td>0.48 (0.45)</td><td>1.15 (1.25)</td><td>1.93 (1.80)</td><td>1.69 (1.65)</td><td>6.88 (6.63)</td></tr><tr><th><b>Leg III</b></th><td>0.24 (0.21)</td><td>0.83 (0.80)</td><td>0.33 (0.33)</td><td>0.60 (0.59)</td><td>1.09 (1.05)</td><td>0.83 (0.83)</td><td>3.93 (3.81)</td></tr><tr><th><b>Leg IV</b></th><td>0.23 (0.21)</td><td>1.33 (1.30)</td><td>0.48 (0.38)</td><td>0.83 (0.83)</td><td>1.59 (1.63)</td><td>0.84 (0.83)</td><td>5.30 (5.18)</td></tr></tbody></table>
Table 8 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
<p><b>Table 8.</b> Length of appendage-segments in millimeters in <i>N. bidentatum gruberi</i> Novak, Slana Novak, Kozel & Raspotnig ssp. nov. from Dolenje Laknice, Slovenia: ♂ holotype (♀).</p><table><tbody><tr><th></th><th><b>Trochanter</b></th><th><b>Femur</b></th><th><b>Patella</b></th><th><b>Tibia</b></th><th><b>Metatarsus</b></th><th><b>Tarsus</b></th><th><b>Total length</b></th></tr></tbody><tbody><tr><th><b>Pedipalp</b></th><td>0.28 (0.31)</td><td>0.77 (0.81)</td><td>0.56 (0.63)</td><td>0.47 (0.49)</td><td>–</td><td>0.30 (0.31)</td><td>2.38 (2.55)</td></tr><tr><th><b>Leg I</b></th><td>0.26 (0.27)</td><td>0.94 (0.83)</td><td>0.39 (0.35)</td><td>0.67 (0.63)</td><td>1.11 (1.04)</td><td>1.10 (0.98)</td><td>4.47 (4.10)</td></tr><tr><th><b>Leg II</b></th><td>0.23 (0.23)</td><td>1.55 (1.40)</td><td>0.47 (0.50)</td><td>0.91 (1.16)</td><td>2.21 (2.24)</td><td>1.80 (1.61)</td><td>7.17 (7.14)</td></tr><tr><th><b>Leg III</b></th><td>0.22 (0.22)</td><td>0.82 (0.83)</td><td>0.36 (0.35)</td><td>0.63 (0.63)</td><td>1.22 (1.19)</td><td>0.97 (0.95)</td><td>4.22 (4.17)</td></tr><tr><th><b>Leg IV</b></th><td>0.23 (0.23)</td><td>1.43 (1.35)</td><td>0.39 (0.41)</td><td>0.79 (0.91)</td><td>1.94 (1.90)</td><td>1.45 (1.23)</td><td>6.23 (6.03)</td></tr></tbody></table>
Table 11 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
<p><b>Table 11.</b> Length of appendage-segments in millimeters in <i>N. bidentatum schmidti</i> Novak, Raspotnig & Slana Novak ssp. nov. from Dolenja Sevnica, Slovenia: ♂ holotype (♀).</p><table><tbody><tr><th></th><th><b>Trochanter</b></th><th><b>Femur</b></th><th><b>Patella</b></th><th><b>Tibia</b></th><th><b>Metatarsus</b></th><th><b>Tarsus</b></th><th><b>Total length</b></th></tr></tbody><tbody><tr><th><b>Pedipalp</b></th><td>0.28 (0.30)</td><td>0.77 (0.83)</td><td>0.45 (0.60)</td><td>0.46 (0.48)</td><td>–</td><td>0.26 (0.33)</td><td>2.22 (2.54)</td></tr><tr><th><b>Leg I</b></th><td>0.21 (0.25)</td><td>0.86 (0.85)</td><td>0.33 (0.35)</td><td>0.63 (0.60)</td><td>0.93 (1.01)</td><td>0.95 (0.99)</td><td>3.91 (4.05)</td></tr><tr><th><b>Leg II</b></th><td>0.23 (0.29)</td><td>1.35 (1.35)</td><td>0.41 (0.49)</td><td>1.12 (1.08)</td><td>1.98 (1.95)</td><td>1.58 (1.63)</td><td>6.67 (6.79)</td></tr><tr><th><b>Leg III</b></th><td>0.22 (0.18)</td><td>0.86 (0.85)</td><td>0.35 (0.35)</td><td>0.59 (0.60)</td><td>1.08 (1.04)</td><td>0.87 (0.78)</td><td>3.97 (3.80)</td></tr><tr><th><b>Leg IV</b></th><td>0.22 (0.26)</td><td>1.32 (1.33)</td><td>0.41 (0.40)</td><td>0.82 (0.81)</td><td>1.60 (1.81)</td><td>1.11 (1.08)</td><td>5.48 (5.69)</td></tr></tbody></table>
TABLE 1 in Early Cretaceous angiosperm leaves from the Dakota Formation, Hoisington III locality, Kansas, USA
<p><b>TABLE 1 (continued).</b></p><table><tbody><tr><th><b>Taxon</b></th><th></th><th><b>Locality</b></th><th></th></tr></tbody><tbody><tr><th><b>Genus/species</b></th><td><b>Hoisington</b></td><td><b>Braun Ranch</b></td><td><b>Rose Creek</b></td><td><b>Courtland</b></td></tr><tr><th><i>Aspidiophyllum denticulatum</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Sapindopsis powelliana</i> comb. nov.</th><td>+</td><td></td><td></td><td></td></tr><tr><th><i>Sapindopsis retallackii</i> sp. nov.</th><td>+</td><td></td><td></td><td></td></tr><tr><th><i>Anisodromum wolfei</i></th><td>+</td><td></td><td>+</td><td></td></tr><tr><th><i>Anisodromum upchurchii</i> sp. nov.</th><td>+</td><td></td><td></td><td></td></tr><tr><th><i>Anisodromum schimperi</i> comb. nov.</th><td>+</td><td></td><td></td><td></td></tr><tr><th><i>Citrophyllum doylei</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Citrophyllum aligera</i></th><td>+</td><td></td><td></td><td></td></tr><tr><th><i>Trochodendroides rhomboideus</i></th><td></td><td></td><td></td><td>+</td></tr><tr><th><i>Trochodendroides elliptica</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Wingia expansolobum</i> comb. nov.</th><td>+</td><td></td><td>+</td><td></td></tr><tr><th><i>Wingia cf. expansolobum</i></th><td>+</td><td></td><td></td><td></td></tr><tr><th><i>Acritodromum ellipticum</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Crepetii minudentis</i></th><td></td><td></td><td></td><td>+</td></tr><tr><th><i>Didromophyllum basingerii</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Glandilunatus kansense</i></th><td></td><td>+</td><td></td><td>+</td></tr><tr><th><i>Gooleria crasseprima</i></th><td></td><td></td><td></td><td>+</td></tr><tr><th><i>Hickeyphyllum sandersii</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Hickeyphyllum imhofii</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Kladoneuron gooleri</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Reynoldsiophyllum masonii</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Reynoldsiophyllum nebrascense</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th>New genus B</th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Dicotylophyllum aliquantuliserratum</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Dicotylophyllum angularis</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Dicotylophyllum braunii</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Dicotylophyllum carlsonii</i></th><td></td><td></td><td></td><td>+</td></tr><tr><th><i>Dicotylophyllum coughlantii</i></th><td></td><td></td><td></td><td>+</td></tr><tr><th><i>Dicotylophyllum fragile</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Dicotylophyllum huangii</i></th><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Dicotylophyllum leptovenum</i></th><td>+</td><td></td><td></td><td>+</td></tr><tr><th><i>Dicotylophyllum myrtophylloides</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Dicotylophyllum rosafluviatilis</i></th><td></td><td></td><td>+</td><td></td></tr><tr><th><i>Dicotylophyllum skogii</i> sp. nov.</th><td>+</td><td></td><td></td><td></td></tr><tr><th><i>Dicotylophyllum tulipiferum</i></th><td></td><td></td><td></td><td>+</td></tr><tr><th>70</th><td>24</td><td>21</td><td>21</td><td>20</td></tr></tbody></table>
Table 7 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
<p><b>Table 7.</b> Length of appendage-segments in millimeters in <i>N. pluridentatum</i> (Hadži, 1973) stat. nov. from Mt. Paljenik, Bosnia and Herzegovina: ♂ holotype, ♀ unknown.</p><table><tbody><tr><th></th><th><b>Trochanter</b></th><th><b>Femur</b></th><th><b>Patella</b></th><th><b>Tibia</b></th><th><b>Metatarsus</b></th><th><b>Tarsus</b></th><th><b>Total length</b></th></tr></tbody><tbody><tr><th><b>Pedipalp</b></th><td>0.27</td><td>0.68</td><td>0.49</td><td>0.38</td><td>–</td><td>0.29</td><td>2.11</td></tr><tr><th><b>Leg I</b></th><td>0.19</td><td>0.60</td><td>0.31</td><td>0.41</td><td>0.50</td><td>0.49</td><td>2.50</td></tr><tr><th><b>Leg II</b></th><td>0.22</td><td>1.05</td><td>0.28</td><td>1.25</td><td>1.05</td><td>0.80</td><td>4.65</td></tr><tr><th><b>Leg III</b></th><td>0.21</td><td>0.70</td><td>0.25</td><td>0.50</td><td>0.65</td><td>0.65</td><td>3.16</td></tr><tr><th><b>Leg IV</b></th><td>0.22</td><td>0.95</td><td>0.25</td><td>0,60</td><td>1,20</td><td>0.75</td><td>3.95</td></tr></tbody></table>
TABLE 2. — Correspondences between the MNHN. F in Fossil wood from the lower Miocene of Myanmar (Natma Formation): palaeoenvironmental and biogeographic implications
<p>TABLE 2. — Correspondences between the MNHN.F specimen numbers cited in the article and the corresponding pages on https://science.mnhn.fr.</p><table><tbody><tr><th>Specimen numbers</th><th><b>Corresponding slides and URLs</b></th></tr></tbody><tbody><tr><th>MNHN. F.50171</th><td>MNHN. F.50171.1, 50171.2, 50171.3, 50171.4, 50171.5, 50171.6, 50171.7</td></tr><tr><th>MNHN. F.50172</th><td>MNHN. F.50172.1, 50172.2, 50172.3</td></tr><tr><th>MNHN. F.50173</th><td>MNHN. F.50173.1, 50173.2, 50173.3</td></tr><tr><th>MNHN. F.50174</th><td>MNHN. F.50174.1, 50174.2, 50174.3</td></tr><tr><th>MNHN. F.50175</th><td>MNHN. F.50175.1, 50175.2, 50175.3, 50175.4, 50175.5</td></tr><tr><th>MNHN. F.50176</th><td>MNHN. F.50176.1, 50176.2, 50176.3</td></tr><tr><th>MNHN. F.50177</th><td>MNHN. F.50177.1, 50177.2, 50177.3</td></tr><tr><th>MNHN. F.50178</th><td>MNHN. F.50178.1, 50178.2, 50178.3</td></tr><tr><th>MNHN. F.50179</th><td>MNHN. F.50179.1, 50179.2, 50179.3</td></tr><tr><th>MNHN. F.50180</th><td>MNHN. F.50180.1, 50180.2, 50180.3, 50180.4</td></tr><tr><th>MNHN. F.50181</th><td>MNHN. F.50181.1, 50181.2, 50181.3</td></tr><tr><th>MNHN. F.50182</th><td>MNHN. F.50182.1, 50182.2, 50182.3</td></tr><tr><th>MNHN. F.50183</th><td>MNHN. F.50183.1, 50183.2, 50183.3</td></tr><tr><th>MNHN. F.50184</th><td>MNHN. F.50184.1, 50184.2, 50184.3, 50184.4, 50184.5, 50184.6</td></tr><tr><th>MNHN. F.50185</th><td>MNHN. F.50185.1, 50185.2, 50185.3</td></tr><tr><th>MNHN. F.50186</th><td>MNHN. F.50186.1, 50186.2, 50186.3, 50186.4</td></tr><tr><th>MNHN. F.50187</th><td>MNHN. F.50187.1, 50187.2, 50187.3</td></tr><tr><th>MNHN. F.50188</th><td>MNHN. F.50188.1, 50188.2, 50188.3, 50188.4, 50188.5, 50188.6</td></tr><tr><th>MNHN. F.50189</th><td>MNHN. F.50189.1, 50189.2, 50189.3, 50189.4, 50189.5, 50189.6</td></tr><tr><th>MNHN. F.50190</th><td>MNHN. F.50190.1, 50190.2, 50190.3</td></tr><tr><th>MNHN. F.50191</th><td>MNHN. F.50191.1, 50191.2, 50191.3, 50191.4, 50191.5, 50191.6</td></tr><tr><th>MNHN. F.50192</th><td>MNHN. F.50192.1, 50192.2, 50192.3</td></tr><tr><th>MNHN. F.50193</th><td>MNHN. F.50193.1, 50193.2, 50193.3, 50193.4, 50193.5, 50193.6</td></tr><tr><th>MNHN. F.50194</th><td>MNHN. F.50194.1, 50194.2, 50194.3</td></tr><tr><th>MNHN. F.50195</th><td>MNHN. F.50195.1, 50195.2, 50195.3</td></tr><tr><th>MNHN. F.50196</th><td>MNHN. F.50196.1, 50196.2, 50196.3</td></tr><tr><th>MNHN. F.50197</th><td>MNHN. F.50197.1, 50197.2, 50197.3</td></tr><tr><th>MNHN. F.50198</th><td>MNHN. F.50198.1, 50198.2, 50198.3</td></tr><tr><th>MNHN. F.50199</th><td>MNHN. F.50199.1, 50199.2, 50199.3, 50199.4</td></tr><tr><th>MNHN. F.50200</th><td>MNHN. F.50200.1, 50200.2, 50200.3, 50200.4, 50200.5</td></tr></tbody></table>
Table 1 in New Eocene South American native ungulates from the Quebrada de los Colorados Formation at Los Cardones National Park, Argentina
<p>Table 1. Measurements (in mm) of the dental specimens. Abbreviations: *, approximate measurements due to the brakeage of the specimen; LLL, labio-lingual length; MDL, mesio-distal length.</p><table><tbody><tr><th>Taxon</th><th>Specimen</th><th>Locus</th><th>MDL</th><th>LLL</th></tr></tbody><tbody><tr><th><i>Astrapotheria</i> indet.</th><td>IBIGEO-P 66</td><td>M1 M2 M3</td><td>>22.62>30.22>35.35</td><td>>30.00>35.42 –</td></tr><tr><th><i>Colbertia lumbrerense</i></th><td>IBIGEO-P 45</td><td>P4 M3</td><td>>4.58 5.62</td><td>>4.44 7.24</td></tr><tr><th></th><td>IBIGEO-P 56</td><td>M1 or M2</td><td>5.43*</td><td>5.17*</td></tr><tr><th></th><td>IBIGEO-P 58a</td><td>M2 M3</td><td>7.28* 7.52*</td><td>– –</td></tr><tr><th><i>Colbertia</i> sp.</th><td>IBIGEO-P 58b</td><td>P4 M1 M2 M3</td><td>5.25* 5.43* 5.45* 6.00*</td><td>7.95 8.40 8.32* 8.00*</td></tr><tr><th>? <i>Homalostylops</i> sp.</th><td>IBIGEO-P 57a</td><td>m1?</td><td>5.85</td><td>4.15</td></tr><tr><th><i>Homalostylops</i> sp.</th><td>IBIGEO-P 57b</td><td>m2?</td><td>7.15</td><td>4.43</td></tr><tr><th></th><td>IBIGEO-P 62</td><td>m1</td><td>>5.77</td><td>4.39*</td></tr><tr><th><i>Pampahippus secundus</i></th><td>IBIGEO-P 63</td><td>p3 or p4</td><td>>7.70</td><td>5.44*</td></tr><tr><th></th><td>IBIGEO-P 64</td><td>m1</td><td>>7.90</td><td>5.00</td></tr><tr><th></th><td>IBIGEO-P 55</td><td>p3 p4</td><td>4.70 5.38</td><td>3.91 4.38</td></tr><tr><th><i>Colbertia falui</i></th><td>IBIGEO-P 59 IBIGEO-P 61</td><td>m2 m3 m2 m3</td><td>6.85 7.83 7.73 9.70</td><td>5.00* 4.53 5.40 4.78</td></tr><tr><th></th><td>IBIGEO-P 67</td><td>m2 m3</td><td>>5.48 7.91</td><td>4.57* 4.30</td></tr></tbody></table>
Table presenting the results of Schmidt hammer tests conducted in the JK-1 cave and the rocky courtyard outside
<p><span>This research was funded by National Science Centre, Poland, research project no. 2020/39/D/ST10/00861.</span></p> <p><span>T</span><span>he table presents the results of Schmidt hammer tests conducted in the JK-1 cave and the rocky courtyard outside. The tests were conducted in the Białe Skały massif, Stołowe Mountains, SW Poland. LW, CW, RW – cave walls; LC, MC – cave ceiling; C – rocky courtyard.</span></p>
TABLE 1 in Fossil wood from the lower Miocene of Myanmar (Natma Formation): palaeoenvironmental and biogeographic implications
<p>TABLE 1. — Distribution of fossil taxa for the Natma Formation among extant tropical forests of the Indo-Burman region, according to their Nearest Living Relatives. Only the most convincing NLR have been taken into consideration. Symbols and abbreviations: ●, main environment; ○, alternative environment; <b>1</b>, Tidal and coastal forests; <b>2</b>, Moist evergreen and semi-evergreen forests; <b>3</b>, Deciduous and seasonal forests; <b>4</b>, Dry forests and savanna woodlands. The specimen of <i>Cupressinoxylon</i> is not used here, as not diagnostic of any particular environment.The specimen indet sp. 1 is shown as an indication of possible relative modern ecosystem because the possible related taxa are mostly found in ecosystems in adequacy with our other specimens.</p><table><tbody><tr><th><b>Fossil species</b></th><th><b>NLR</b></th><th><b>Modern ecosystems</b></th><th><b>1</b></th><th><b>2</b></th><th><b>3</b></th><th><b>4</b></th><th><b>Forest type</b></th></tr></tbody><tbody><tr><th><i>Cynometroxylon holdeniae</i></th><td><i>Cynometra ramiflora</i> / <i>Cynometra polyandra</i></td><td>Tidal, back-mangrove, wet evergreen and semi-evergreen forests. In lowlands</td><td>●</td><td>○</td><td>–</td><td>–</td><td></td></tr><tr><th></th><td></td><td>up to 400-1300 m</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Cynometroxylon parainaequifolium</i></th><td><i>Cynometra inaequifolia</i> / <i>Cynometra polyandra</i></td><td>Tidal, back-mangrove, wet evergreen and semi-evergreen forests. In lowlands</td><td>●</td><td>○</td><td>–</td><td>–</td><td>Coastal forests</td></tr><tr><th></th><td></td><td>up to 400-1300 m</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Pahudioxylon bankurensis</i></th><td><i>Intsia bijuga</i></td><td>Coastal areas, along tidal rivers or at the dry back of mangroves. Also wet evergreen forest</td><td>●</td><td>●</td><td>–</td><td>○</td><td></td></tr><tr><th></th><td></td><td>associated with Anisoptera. Up to 600 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>indet sp. 1</th><td><i>Dipterocarpus</i> / <i>Prioria</i></td><td>Wet evergreen forests, coastal forests, flooded and riparian forests, also in semi-evergeen</td><td>●</td><td>●</td><td>○</td><td>○</td><td>?</td></tr><tr><th></th><td></td><td>forest or savannahs. In lowlands.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Dryobalanoxylon</i> sp.</th><td><i>Dryobalanops aromatica</i> / <i>D. oblongifolia</i></td><td>Lowland mixed dipterocarp forests, in coastal areas in sandy or gravelly soils. Also in wetter</td><td>●</td><td>●</td><td>○</td><td>–</td><td></td></tr><tr><th></th><td></td><td>soils. Up to 600 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>cf. Koompassioxylon</th><td><i>Koompassia</i> / <i>Kalappia</i> / <i>Martiodendron</i></td><td>Mostly rainforest. Also in coastal forest, riparian forests or swamps. Rarely in savannas or dry</td><td>○</td><td>●</td><td>–</td><td>○</td><td></td></tr><tr><th></th><td></td><td>forests. Up to 600 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Koompassioxylon elegans</i></th><td><i>Koompassia malaccensis</i></td><td>Mostly freshwater peat-swamps. Also dry lands. Up to 150 m (800 m in elevated areas)</td><td>–</td><td>●</td><td>–</td><td>○</td><td></td></tr><tr><th><i>Burseroxylon</i> sp.</th><td><i>Canarium bengalense</i> / <i>Protium serratum</i></td><td>Wet evergreen and moist dipterocarp forests, mostly along rivers. Also in deciduous forests</td><td>–</td><td>●</td><td>○</td><td>–</td><td></td></tr><tr><th></th><td></td><td>or monsonnal area. Up to 1300 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Anisopteroxylon</i> sp.</th><td><i>Anisoptera costata</i> / <i>Anisoptera scaphula</i></td><td>Moist (not everwet) evergreen and semi- evergreen dipterocarp forests, along rivers,</td><td>–</td><td>●</td><td>○</td><td>–</td><td></td></tr><tr><th></th><td></td><td>in seasonal forest and foothills. Up to 700 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Dipterocarpoxylon</i> cf. <i>jammuense</i></th><td><i>Dipterocarpus</i></td><td>Evergreen, semi-evergeen tropical forest, mixed dipterocarps forests. Also in seasonal forests.</td><td>–</td><td>●</td><td>○</td><td>–</td><td>Wet evergreen forests</td></tr><tr><th></th><td></td><td>In lowland (rarely up to 1400 m).</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Dryobalanoxylon</i> cf. <i>javanense</i></th><td><i>Dryobalanops keithii</i> / <i>D. oblongifolia</i></td><td>Near water (periodically inundated, streams, poorly-drained soils...), in mixed dipterocarps</td><td>–</td><td>●</td><td>○</td><td>–</td><td></td></tr><tr><th></th><td></td><td>forests. Up to 600 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Shoreoxylon</i> cf. <i>sumatraense</i></th><td><i>Shorea negrosensis</i></td><td>Evergreen, semi-evergreen and seasonal dipterocarp forests. In lowlands.</td><td>–</td><td>●</td><td>○</td><td>–</td><td></td></tr><tr><th><i>Shoreoxylon</i> cf. <i>deomaliense</i></th><td><i>Shorea laevis</i></td><td>Mixed dipterocarp forests. On undulated lands and well-drained soils. Up to 700-1000 m.</td><td>–</td><td>●</td><td>○</td><td>–</td><td></td></tr><tr><th><i>Artocarpoxylon kartikcherraensis</i></th><td><i>Artocarpus lamellosus</i> / <i>Artocarpus chama</i></td><td>Mixed dipterocarp evergreen forests, but also in semi-deciduous forests, moist deciduous</td><td>–</td><td>●</td><td>○</td><td>○</td><td></td></tr><tr><th></th><td></td><td>or monsoonal area. Up to 1500-1800 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Shoreoxylon</i> sp. 2</th><td><i>Shorea balangeran</i> / <i>Shorea laevis</i></td><td>From well-drained soils to peat-swamp forests. Also in lowland mixed dipterocarp forests</td><td>–</td><td>●</td><td>●</td><td>–</td><td></td></tr><tr><th></th><td></td><td>and hillsides. Up to 100(-1000)m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Albizinium eolebbekianum</i></th><td><i>Albizia lebbeck</i> / <i>Albizia ferruginea</i></td><td>Wooded savannas, dry forests borders, semi- decidous. Also rainforests, riparian or</td><td>○</td><td>○</td><td>●</td><td>○</td><td></td></tr><tr><th></th><td></td><td>periodically inundeted ofrests. Up to 1400 m.</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Pahudioxylon</i> cf. <i>bankurensis</i></th><td><i>Afzelia africana</i> / <i>A. javanica</i></td><td>Both present in humid evergreen and dry deciduous forests. Frequent in savannas. Up</td><td>–</td><td>○</td><td>●</td><td>○</td><td>Seasonal and</td></tr><tr><th></th><td></td><td>to 1400 m.</td><td></td><td></td><td></td><td></td><td>dry forests</td></tr><tr><th><i>Shoreoxylon</i> sp. 1</th><td><i>Shorea parvifolia</i> /</td><td>Deciduous dry dipterocarp forests and under</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td><i>Shorea obtusa</i></td><td>marked seasonal monsoon climates. Sometimes in moister forests or savannas.</td><td>–</td><td>○</td><td>●</td><td>●</td><td></td></tr><tr><th></th><td></td><td>Up to 1000 m.</td><td></td><td></td><td></td><td></td><td></td></tr></tbody></table>
Source code of tables for the publication "K- and L-shell theoretical fluorescence yields for the Fe isonuclear sequence"
<p>In this work, we present K- and L- shell fluorescence yield values of the full isonuclear sequence of Fe ions, using a state-of-the-art multiconfiguration Dirac-Fock approach. These results may be of importance for spectral fitting and plasma modeling, both in laboratory and astrophysical studies, where Fe is an important benchmark element. The K-shell fluorescence yields were found to be very similar up to the removal of 14 electrons.</p>
Supplementary Table S1. Combined analysis of variance containing the degrees of freedom (DF), mean squares (MS), P value (P val.), mean, coefficient of experimental variation (CEV%) and selective accuracy (SA) for the traits of luminosity (L*), chromaticity a* (a*), chromaticity b* (b*), grain length (length, mm), grain width (width, mm), grain thickness (thickness, mm), mass of 100 grains (Mass, g), normal grains (Ng, %), water absorption (absorption, %), cooking time (Ct, min:s), and concentrations of potassium (K, g kg-1 dry matter - DM), phosphorus (P, g kg-1 DM), calcium (Ca, g kg-1 DM), magnesium (Mg, g kg-1 DM), iron (Fe, mg kg-1 DM), zinc (Zn, mg kg-1 DM), and copper (Cu, mg kg-1 DM) obtained in 25 common bean cultivars evaluated in four experiments carried out from 2019 to 2021
<p><strong><span>Table S1.</span></strong><span> Combined analysis of variance.</span></p> <p><strong><span>Indirect selection for multiple technological and nutritional traits in common bean cultivars under different degrees of multicollinearity</span></strong></p> <p><strong><span>Bragantia, 2024.</span></strong></p>
Table 3 in Fig. 11. Left G 1 s in Tuerkayana latens, a New Species of Land Crab from French Polynesia, with a Discussion on the Phylogeny of the Genus (Crustacea: Decapoda: Brachyura: Gecarcinidae)
<p><b>Table 3.</b> The frequency of contribution of environmental variables in predicting the clades geographic distribution models</p><table><tbody><tr><th>Environmental variable (unit)</th><th>Clade <i>I</i></th><th>Clade <i>III</i></th></tr></tbody><tbody><tr><th>Temperature Mean</th><td>39.8</td><td>56.8</td></tr><tr><th>Temperature Range</th><td>25.7</td><td>4.9</td></tr><tr><th>Phytoplankton Mean</th><td>15.3</td><td>5.9</td></tr><tr><th>Salinity Mean</th><td>5.5</td><td>1.4</td></tr><tr><th>Salinity Range</th><td>3.9</td><td>6.2</td></tr><tr><th>Current Velocity Mean</th><td>2.7</td><td>3.7</td></tr><tr><th>Current Velocity Ltmax</th><td>2</td><td>0</td></tr><tr><th>Dissolved oxygen Range</th><td>1.9</td><td>1.6</td></tr><tr><th>Phosphate Mean</th><td>1.6</td><td>5.3</td></tr><tr><th>Current Velocity Min</th><td>1</td><td>14.2</td></tr><tr><th>Current Velocity Max</th><td>0.6</td><td>0</td></tr></tbody></table>
Table 2 in Fig. 11. Left G 1 s in Tuerkayana latens, a New Species of Land Crab from French Polynesia, with a Discussion on the Phylogeny of the Genus (Crustacea: Decapoda: Brachyura: Gecarcinidae)
<p><b>Table 2.</b> Pairwise estimates of <i>COI</i> genetic divergence (Φ ST) for <i>Amphibalanus amphitrite</i> among five biogeographical areas. The significance of ΦST values was tested by a permutation test with 1000 replicates</p><table><tbody><tr><th></th><th>MK(PG)</th><th>TH(PG)</th><th>GU(GO)</th><th>CH(GO)</th><th>JS(GO)</th></tr></tbody><tbody><tr><th>MK(PG)</th><td>0</td><td></td><td></td><td></td><td></td></tr><tr><th>TH(PG)</th><td>0.00748</td><td>0</td><td></td><td></td><td></td></tr><tr><th>GU(GO)</th><td>0.00728</td><td>0.03051*</td><td>0</td><td></td><td></td></tr><tr><th>CH(GO)</th><td>0.03196*</td><td>0.00921</td><td>0.01027</td><td>0</td><td></td></tr><tr><th>JS(GO)</th><td>0.01838</td><td>0.00420</td><td>0.00528</td><td>0.02062</td><td>0</td></tr></tbody></table><p>* <i>p</i> <0.05.</p>
Table 5 in Newly discovered species of cheilostomatid Bryozoa from the Miocene of western Kachchh, Gujarat, India
<p><b>Table 5.</b> Measurements in mm of <i>Cupuladria</i> sp. (GIS/B 0471 to 0503), Aquitanian, lower Miocene, Kharinadi Formation, western Kachchh, Gujarat, India. Abbreviations: see Material and methods.</p><table><thead><tr><th></th><th><b>Minimum</b></th><th><b>Maximum</b></th><th><b>Mean</b></th><th><b>SD</b></th><th><b>N</b></th></tr></thead><tbody><tr><th>LZ</th><td>0.140</td><td>0.160</td><td>0.152</td><td>± 0.005</td><td>10</td></tr><tr><th>WZ</th><td>0.100</td><td>0.110</td><td>0.104</td><td>± 0.001</td><td>10</td></tr><tr><th>LOp</th><td>0.070</td><td>0.090</td><td>0.081</td><td>± 0.004</td><td>10</td></tr><tr><th>WOp</th><td>0.050</td><td>0.070</td><td>0.060</td><td>± 0.004</td><td>10</td></tr><tr><th>LZ</th><td>0.223</td><td>0.241</td><td>0.233</td><td>± 0.007</td><td>10</td></tr><tr><th>WZ</th><td>0.090</td><td>0.109</td><td>0.102</td><td>± 0.006</td><td>10</td></tr><tr><th>LOr</th><td>0.043</td><td>0.051</td><td>0.048</td><td>± 0.002</td><td>05</td></tr><tr><th>WOr</th><td>0.020</td><td>0.032</td><td>0.028</td><td>± 0.003</td><td>05</td></tr></tbody></table>
Table 1 in Review of the plant bug tribe Eccritotarsini (Hemiptera: Heteroptera: Miridae) of India and Sri Lanka with description of two new genera and six new species
<p><b>Table 1 (continued on next page).</b> Measurements (mm) of eccritotarsine specimens examined for this study. Abbreviations: Clyp/Cun = distance between apex of clypeus and apex of cuneus in dorsal view; InterOcDi = width of vertex between inner margins of eyes in dorsal view.</p><table><thead><tr><th></th><th></th><th colspan="11"><b>Length</b></th><th colspan="5"><b>Width</b></th></tr></thead><tbody><tr><th colspan="2"><b>Specimens</b></th><td><b>Body</b></td><td><b>Clyp/ Cun.</b></td><td><b>Head</b></td><td><b>Pron.</b></td><td colspan="2"><b>Scut. Cun.</b></td><td colspan="4"><b>Antennal segments I II III IV</b></td><td><b>Labium</b></td><td><b>Head</b></td><td><b>Pron.</b></td><td colspan="2"><b>Scut. InterOcDi</b></td><td><b>Body</b></td></tr><tr><th></th><td colspan="17"><b><i>Dioclerus bengalicus</i> Stonedahl, 1988</b></td></tr><tr><th>♀, <b>N=1</b></th><td></td><td>3.46</td><td>2.55</td><td>0.25</td><td>0.66</td><td>0.38</td><td>0.41</td><td>0.56</td><td>1.11</td><td>0.47</td><td>0.44</td><td>0.80</td><td>0.80</td><td>1.15</td><td>0.52</td><td>0.38</td><td>1.48</td></tr><tr><th></th><td colspan="17"><b><i>Dioclerus lutheri</i> Poppius, 1912</b></td></tr><tr><th>♂, <b>N=1</b></th><td></td><td>3.42</td><td>2.63</td><td>0.25</td><td>0.74</td><td>0.40</td><td>0.39</td><td>0.62</td><td>1.09</td><td>0.45</td><td>0.63</td><td>0.91</td><td>0.88</td><td>1.19</td><td>0.60</td><td>0.44</td><td>1.42</td></tr><tr><th></th><td colspan="17"><b><i>Ernestinus ramkeshariae</i> Yasunaga & Ishikawa, 2016</b></td></tr><tr><th rowspan="4">♂, N=3</th><td rowspan="4"><b>Max</b> <b>Min</b> <b>Mean</b> <b>SD</b></td><td>3.25</td><td>2.28</td><td>0.19</td><td>0.80</td><td>0.34</td><td>0.54</td><td>0.36</td><td>0.63</td><td>0.64</td><td>0.64</td><td>0.78</td><td>0.59</td><td>1.23</td><td>0.43</td><td>0.34</td><td>1.26</td></tr><tr><td>3.10</td><td>2.14</td><td>0.17</td><td>0.74</td><td>0.28</td><td>0.52</td><td>0.35</td><td>0.56</td><td>0.59</td><td>0.56</td><td>0.74</td><td>0.56</td><td>1.01</td><td>0.37</td><td>0.31</td><td>1.14</td></tr><tr><td>3.17</td><td>2.21</td><td>0.18</td><td>0.78</td><td>0.31</td><td>0.53</td><td>0.35</td><td>0.60</td><td>0.00</td><td>0.00</td><td>0.76</td><td>0.57</td><td>1.11</td><td>0.40</td><td>0.33</td><td>1.18</td></tr><tr><td>0.06</td><td>0.05</td><td>0.01</td><td>0.02</td><td>0.02</td><td>0.01</td><td>0.00</td><td>0.03</td><td>0.00</td><td>0.00</td><td>0.02</td><td>0.01</td><td>0.10</td><td>0.02</td><td>0.01</td><td>0.05</td></tr><tr><th rowspan="4">♀, <b>N=3</b></th><td rowspan="4"><b>Max</b> Min <b>Mean</b> <b>SD</b></td><td>3.55</td><td>2.43</td><td>0.15</td><td>0.82</td><td>0.29</td><td>0.56</td><td>0.33</td><td>0.56</td><td>0.57</td><td>0.66</td><td>1.00</td><td>0.58</td><td>1.10</td><td>0.46</td><td>0.34</td><td>1.38</td></tr><tr><td>3.40</td><td>2.34</td><td>0.14</td><td>0.78</td><td>0.27</td><td>0.50</td><td>0.32</td><td>0.55</td><td>0.52</td><td>0.61</td><td>0.79</td><td>0.55</td><td>1.00</td><td>0.41</td><td>0.30</td><td>1.20</td></tr><tr><td>3.47</td><td>2.39</td><td>0.15</td><td>0.79</td><td>0.28</td><td>0.52</td><td>0.32</td><td>0.55</td><td>0.56</td><td>0.63</td><td>0.90</td><td>0.56</td><td>1.03</td><td>0.43</td><td>0.32</td><td>1.29</td></tr><tr><td>0.06</td><td>0.04</td><td>0.00</td><td>0.02</td><td>0.01</td><td>0.03</td><td>0.01</td><td>0.00</td><td>0.02</td><td>0.02</td><td>0.08</td><td>0.01</td><td>0.05</td><td>0.02</td><td>0.02</td><td>0.07</td></tr><tr><th></th><td colspan="17"><b><i>Ernestinus mimicus</i> Distant, 1911</b></td></tr><tr><th rowspan="4">♂, <b>N=3</b></th><td rowspan="4"><b>Max</b> Min <b>Mean</b> <b>SD</b></td><td>3.11</td><td>2.06</td><td>0.18</td><td>0.70</td><td>0.26</td><td>0.50</td><td>0.35</td><td>0.78</td><td>0.59</td><td>0.44</td><td>1.00</td><td>0.60</td><td>0.97</td><td>0.42</td><td>0.35</td><td>1.12</td></tr><tr><td>2.74</td><td>1.96</td><td>0.13</td><td>0.62</td><td>0.24</td><td>0.48</td><td>0.32</td><td>0.77</td><td>0.55</td><td>0.43</td><td>0.90</td><td>0.58</td><td>0.97</td><td>0.40</td><td>0.34</td><td>1.01</td></tr><tr><td>2.87</td><td>2.00</td><td>0.15</td><td>0.66</td><td>0.25</td><td>0.49</td><td>0.33</td><td>0.77</td><td>0.57</td><td>0.44</td><td>0.96</td><td>0.59</td><td>0.97</td><td>0.40</td><td>0.35</td><td>1.06</td></tr><tr><td>0.14</td><td>0.04</td><td>0.02</td><td>0.04</td><td>0.01</td><td>0.01</td><td>0.01</td><td>0.00</td><td>0.01</td><td>0.01</td><td>0.04</td><td>0.01</td><td>0.00</td><td>0.01</td><td>0.00</td><td>0.05</td></tr><tr><th rowspan="4">♀, <b>N=3</b></th><td rowspan="4"><b>Max</b> Min <b>Mean</b> <b>SD</b></td><td>3.43</td><td>2.96</td><td>0.18</td><td>0.72</td><td>0.31</td><td>0.54</td><td>0.36</td><td>0.72</td><td>0.51</td><td>0.49</td><td>1.05</td><td>0.64</td><td>1.07</td><td>0.49</td><td>0.38</td><td>1.30</td></tr><tr><td>3.28</td><td>2.31</td><td>0.17</td><td>0.69</td><td>0.30</td><td>0.50</td><td>0.32</td><td>0.67</td><td>0.47</td><td>0.43</td><td>1.00</td><td>0.60</td><td>1.01</td><td>0.45</td><td>0.36</td><td>1.16</td></tr><tr><td>3.34</td><td>2.49</td><td>0.17</td><td>0.71</td><td>0.30</td><td>0.52</td><td>0.35</td><td>0.69</td><td>0.49</td><td>0.46</td><td>1.02</td><td>0.61</td><td>1.04</td><td>0.47</td><td>0.36</td><td>1.23</td></tr><tr><td>0.06</td><td>0.26</td><td>0.00</td><td>0.01</td><td>0.01</td><td>0.02</td><td>0.02</td><td>0.02</td><td>0.01</td><td>0.02</td><td>0.02</td><td>0.01</td><td>0.02</td><td>0.01</td><td>0.01</td><td>0.05</td></tr><tr><th></th><td colspan="17"><b><i>Harpedona sanguinipes</i> Distant, 1909</b></td></tr><tr><th rowspan="4">♂, <b>N=3</b></th><td rowspan="4"><b>Max</b> Min <b>Mean</b> <b>SD</b></td><td>3.82</td><td>2.75</td><td>0.41</td><td>0.71</td><td>0.47</td><td>0.58</td><td>0.37</td><td>0.85</td><td>0.43</td><td>0.39</td><td>1.40</td><td>0.77</td><td>1.09</td><td>0.59</td><td>0.74</td><td>1.10</td></tr><tr><td>3.56</td><td>2.52</td><td>0.35</td><td>0.62</td><td>0.44</td><td>0.53</td><td>0.32</td><td>0.75</td><td>0.42</td><td>0.32</td><td>1.20</td><td>0.72</td><td>1.00</td><td>0.49</td><td>0.47</td><td>1.03</td></tr><tr><td>3.67</td><td>2.64</td><td>0.39</td><td>0.68</td><td>0.45</td><td>0.55</td><td>0.35</td><td>0.81</td><td>0.00</td><td>0.00</td><td>1.30</td><td>0.75</td><td>1.06</td><td>0.53</td><td>0.56</td><td>1.06</td></tr><tr><td>0.13</td><td>0.12</td><td>0.03</td><td>0.05</td><td>0.02</td><td>0.02</td><td>0.02</td><td>0.05</td><td>0.00</td><td>0.00</td><td>0.10</td><td>0.03</td><td>0.05</td><td>0.05</td><td>0.15</td><td>0.04</td></tr><tr><th rowspan="4">♀, <b>N=3</b></th><td rowspan="4"><b>Max</b> Min <b>Mean</b> <b>SD</b></td><td>3.80</td><td>2.76</td><td>0.42</td><td>0.74</td><td>0.56</td><td>0.60</td><td>0.34</td><td>0.74</td><td>0.55</td><td>0.60</td><td>1.60</td><td>0.80</td><td>1.20</td><td>0.68</td><td>0.51</td><td>1.10</td></tr><tr><td>3.43</td><td>2.69</td><td>0.32</td><td>0.66</td><td>0.48</td><td>0.51</td><td>0.32</td><td>0.71</td><td>0.51</td><td>0.54</td><td>1.50</td><td>0.66</td><td>1.10</td><td>0.61</td><td>0.47</td><td>1.02</td></tr><tr><td>3.63</td><td>2.73</td><td>0.38</td><td>0.70</td><td>0.52</td><td>0.55</td><td>0.33</td><td>0.72</td><td>0.00</td><td>0.00</td><td>1.53</td><td>0.75</td><td>1.14</td><td>0.64</td><td>0.49</td><td>1.06</td></tr><tr><td>0.19</td><td>0.04</td><td>0.05</td><td>0.04</td><td>0.04</td><td>0.05</td><td>0.01</td><td>0.02</td><td>0.00</td><td>0.00</td><td>0.06</td><td>0.08</td><td>0.05</td><td>0.04</td><td>0.02</td><td>0.04</td></tr><tr><th></th><td colspan="17"><b><i>Harpedona vittlaensis</i> sp. nov.</b></td></tr><tr><th>♂, <b>N=1</b></th><td></td><td>3.12</td><td>2.28</td><td>0.26</td><td>0.65</td><td>0.39</td><td>0.46</td><td>0.37</td><td>0.89</td><td></td><td></td><td>1.40</td><td>0.77</td><td>1.07</td><td>0.61</td><td>0.42</td><td>1.10</td></tr><tr><th>♀, <b>N=1</b></th><td></td><td>3.21</td><td>2.28</td><td>0.25</td><td>0.62</td><td>0.35</td><td>0.45</td><td>0.34</td><td>0.68</td><td>0.46</td><td>0.39</td><td>1.23</td><td>0.74</td><td>1.10</td><td>0.50</td><td>0.40</td><td>1.11</td></tr><tr><th></th><td colspan="12"><b>Length</b></td><td colspan="5"><b>Width</b></td></tr><tr><th><b>Specimens</b></th><td></td><td><b>Body</b></td><td><b>Clyp./ Cun.</b></td><td><b>Head</b></td><td><b>Pron.</b></td><td colspan="2"><b>Scut. Cun.</b></td><td colspan="4"><b>Antennal segments I II III IV</b></td><td><b>Labium</b></td><td><b>Head</b></td><td><b>Pron.</b></td><td colspan="2"><b>Scut. InterOcDi</b></td><td><b>Body</b></td></tr><tr><th colspan="18"><b><i>Harpedona vittlaensis</i> sp. nov.</b></th></tr><tr><th>♂, <b>N=1</b></th><td></td><td>3.12</td><td>2.28</td><td>0.26</td><td>0.65</td><td>0.39</td><td>0.46</td><td>0.37</td><td>0.89</td><td></td><td></td><td>1.40</td><td>0.77</td><td>1.07</td><td>0.61</td><td>0.42</td><td>1.10</td></tr><tr><th>♀, <b>N=1</b></th><td></td><td>3.21</td><td>2.28</td><td>0.25</td><td>0.62</td><td>0.35</td><td>0.45</td><td>0.34</td><td>0.68</td><td>0.46</td><td>0.39</td><td>1.23</td><td>0.74</td><td>1.10</td><td>0.50</td><td>0.40</td><td>1.11</td></tr><tr><th colspan="18"><b><i>Lopidolon dandeliensis</i> sp. nov.</b></th></tr><tr><th rowspan="4">♂, N=3</th><td><b>Max</b></td><td>5.28</td><td>3.88</td><td>0.49</td><td>1.04</td><td>0.90</td><td>0.96</td><td>0.58</td><td>1.39</td><td>0.58</td><td>0.24</td><td>2.27</td><td>1.16</td><td>1.83</td><td>1.43</td><td>0.55</td><td>2.32</td></tr><tr><td><b>Min</b></td><td>4.91</td><td>3.57</td><td>0.42</td><td>0.95</td><td>0.82</td><td>0.93</td><td>0.50</td><td>1.32</td><td>0.48</td><td>0.24</td><td>2.12</td><td>1.09</td><td>1.83</td><td>1.38</td><td>0.52</td><td>2.19</td></tr><tr><td><b>Mean</b></td><td>5.12</td><td>3.74</td><td>0.44</td><td>0.99</td><td>0.86</td><td>0.94</td><td>0.54</td><td>1.35</td><td>0.53</td><td>0.24</td><td>2.19</td><td>1.12</td><td>1.83</td><td>1.40</td><td>0.53</td><td>2.24</td></tr><tr><td><b>SD</b></td><td>0.19</td><td>0.16</td><td>0.04</td><td>0.05</td><td>0.04</td><td>0.01</td><td>0.04</td><td>0.03</td><td>0.07</td><td>0.00</td><td>0.07</td><td>0.03</td><td>0.00</td><td>0.03</td><td>0.02</td><td>0.07</td></tr><tr><th rowspan="4"><b>♀, N=2</b></th><td><b>Max</b></td><td>5.12</td><td>3.83</td><td>0.50</td><td>0.82</td><td>0.81</td><td>0.92</td><td>0.55</td><td>1.08</td><td>0.53</td><td>0.39</td><td>2.23</td><td>1.10</td><td>1.68</td><td>1.26</td><td>0.61</td><td>2.10</td></tr><tr><td>Min</td><td>5.00</td><td>3.72</td><td>0.48</td><td>0.77</td><td>0.80</td><td>0.91</td><td>0.51</td><td>1.05</td><td>0.53</td><td>0.34</td><td>2.19</td><td>1.06</td><td>1.54</td><td>1.23</td><td>0.60</td><td>2.02</td></tr><tr><td><b>Mean</b></td><td>5.06</td><td>3.78</td><td>0.49</td><td>0.79</td><td>0.81</td><td>0.92</td><td>0.53</td><td>1.06</td><td>0.00</td><td>0.00</td><td>2.21</td><td>1.08</td><td>1.61</td><td>1.25</td><td>0.60</td><td>2.06</td></tr><tr><td><b>SD</b></td><td>0.08</td><td>0.08</td><td>0.01</td><td>0.04</td><td>0.01</td><td>0.01</td><td>0.03</td><td>0.03</td><td>0.00</td><td>0.00</td><td>0.03</td><td>0.03</td><td>0.10</td><td>0.02</td><td>0.01</td><td>0.06</td></tr><tr><th colspan="18"><b><i>Mertila rubrocephala</i> sp nov.</b></th></tr><tr><th rowspan="4"><b>♂, N=3</b></th><td><b>Max</b></td><td>5.54</td><td>3.86</td><td>0.53</td><td>1.10</td><td>0.72</td><td>0.97</td><td>0.66</td><td>1.20</td><td>0.00</td><td>0.00</td><td>2.53</td><td>1.26</td><td>2.10</td><td>1.29</td><td>0.55</td><td>2.52</td></tr><tr><td>Min</td><td>5.28</td><td>3.76</td><td>0.49</td><td>0.98</td><td>0.67</td><td>0.95</td><td>0.55</td><td>1.08</td><td>0.00</td><td>0.00</td><td>2.43</td><td>1.24</td><td>2.04</td><td>1.19</td><td>0.50</td><td>2.50</td></tr><tr><td><b>Mean</b></td><td>5.39</td><td>3.80</td><td>0.51</td><td>1.04</td><td>0.69</td><td>0.96</td><td>0.63</td><td>1.13</td><td>0.00</td><td>0.00</td><td>2.47</td><td>1.25</td><td>2.08</td><td>1.26</td><td>0.53</td><td>2.51</td></tr><tr><td><b>SD</b></td><td>0.12</td><td>0.05</td><td>0.02</td><td>0.05</td><td>0.02</td><td>0.01</td><td>0.06</td><td>0.05</td><td>0.00</td><td>0.00</td><td>0.05</td><td>0.01</td><td>0.03</td><td>0.04</td><td>0.02</td><td>0.01</td></tr><tr><th colspan="18"><b><i>Namyatovia castlerockensis</i> sp. nov</b></th></tr><tr><th rowspan="4">♂, N=3</th><td><b>Max</b></td><td>3.63</td><td>2.60</td><td>0.29</td><td>0.57</td><td>0.37</td><td>1.01</td><td>0.47</td><td>0.70</td><td>0.49</td><td>0.56</td><td>1.09</td><td>0.75</td><td>1.07</td><td>0.66</td><td>0.37</td><td>1.31</td></tr><tr><td><b>Min</b></td><td>3.27</td><td>2.41</td><td>0.26</td><td>0.47</td><td>0.32</td><td>0.92</td><td>0.39</td><td>0.62</td><td>0.46</td><td>0.53</td><td>0.96</td><td>0.70</td><td>0.96</td><td>0.58</td><td>0.37</td><td>1.12</td></tr><tr><td><b>Mean</b></td><td>3.42</td><td>2.49</td><td>0.28</td><td>0.52</td><td>0.35</td><td>0.97</td><td>0.42</td><td>0.66</td><td>0.47</td><td>0.55</td><td>1.01</td><td>0.72</td><td>1.01</td><td>0.60</td><td>0.37</td><td>1.23</td></tr><tr><td><b>SD</b></td><td>0.19</td><td>0.10</td><td>0.01</td><td>0.05</td><td>0.03</td><td>0.05</td><td>0.05</td><td>0.04</td><td>0.01</td><td>0.02</td><td>0.07</td><td>0.03</td><td>0.06</td><td>0.05</td><td>0.00</td><td>0.10</td></tr><tr><th colspan="18"><b><i>Namyatovia sirsiensis</i> sp. nov</b></th></tr><tr><th rowspan="4"><b>♂, N=3</b></th><td><b>Max</b></td><td>3.63</td><td>2.60</td><td>0.29</td><td>0.57</td><td>0.37</td><td>1.01</td><td>0.47</td><td>0.70</td><td>0.49</td><td>0.56</td><td>1.09</td><td>0.75</td><td>1.07</td><td>0.66</td><td>0.37</td><td>1.31</td></tr><tr><td>Min</td><td>3.27</td><td>2.41</td><td>0.26</td><td>0.47</td><td>0.32</td><td>0.92</td><td>0.39</td><td>0.62</td><td>0.46</td><td>0.53</td><td>0.96</td><td>0.70</td><td>0.96</td><td>0.58</td><td>0.37</td><td>1.12</td></tr><tr><td><b>Mean</b></td><td>3.42</td><td>2.49</td><td>0.28</td><td>0.52</td><td>0.35</td><td>0.97</td><td>0.42</td><td>0.66</td><td>0.47</td><td>0.55</td><td>1.01</td><td>0.72</td><td>1.01</td><td>0.60</td><td>0.37</td><td>1.23</td></tr><tr><td><b>SD</b></td><td>0.19</td><td>0.10</td><td>0.01</td><td>0.05</td><td>0.03</td><td>0.05</td><td>0.05</td><td>0.04</td><td>0.01</td><td>0.02</td><td>0.07</td><td>0.03</td><td>0.06</td><td>0.05</td><td>0.00</td><td>0.10</td></tr><tr><th colspan="18"><b><i>Stonedahlia mishmiensis</i> sp. nov.</b></th></tr><tr><th rowspan="4"><b>♂, N=3</b></th><td><b>Max</b></td><td>4.62</td><td>2.96</td><td>0.31</td><td>0.77</td><td>0.38</td><td>1.10</td><td>0.61</td><td>1.21</td><td>1.10</td><td>0.56</td><td>1.20</td><td>0.64</td><td>1.20</td><td>0.60</td><td>0.45</td><td>1.50</td></tr><tr><td>Min</td><td>4.42</td><td>2.80</td><td>0.26</td><td>0.68</td><td>0.31</td><td>1.00</td><td>0.52</td><td>1.10</td><td>0.97</td><td>0.50</td><td>1.10</td><td>0.60</td><td>1.00</td><td>0.53</td><td>0.34</td><td>1.39</td></tr><tr><td><b>Mean</b></td><td>4.50</td><td>2.88</td><td>0.29</td><td>0.73</td><td>0.36</td><td>1.06</td><td>0.56</td><td>1.16</td><td>1.01</td><td>0.52</td><td>1.16</td><td>0.62</td><td>1.10</td><td>0.55</td><td>0.37</td><td>1.44</td></tr><tr><td><b>SD</b></td><td>0.07</td><td>0.07</td><td>0.02</td><td>0.04</td><td>0.03</td><td>0.04</td><td>0.04</td><td>0.05</td><td>0.05</td><td>0.03</td><td>0.04</td><td>0.02</td><td>0.08</td><td>0.03</td><td>0.05</td><td>0.04</td></tr><tr><th rowspan="4">♀, N=33</th><td><b>Max</b></td><td>4.73</td><td>3.14</td><td>0.32</td><td>0.87</td><td>0.39</td><td>1.15</td><td>0.65</td><td>1.24</td><td>1.13</td><td>0.63</td><td>1.23</td><td>0.65</td><td>1.24</td><td>0.60</td><td>0.39</td><td>1.59</td></tr><tr><td><b>Min</b></td><td>4.43</td><td>3.00</td><td>0.29</td><td>0.78</td><td>0.35</td><td>1.00</td><td>0.60</td><td>1.16</td><td>0.95</td><td>0.50</td><td>1.12</td><td>0.60</td><td>1.16</td><td>0.45</td><td>0.36</td><td>1.51</td></tr><tr><td><b>Mean</b></td><td>4.54</td><td>3.07</td><td>0.30</td><td>0.83</td><td>0.37</td><td>1.08</td><td>0.63</td><td>1.20</td><td>1.03</td><td>0.57</td><td>1.18</td><td>0.63</td><td>1.20</td><td>0.52</td><td>0.37</td><td>1.54</td></tr><tr><td><b>SD</b></td><td>0.12</td><td>0.05</td><td>0.01</td><td>0.03</td><td>0.02</td><td>0.06</td><td>0.02</td><td>0.03</td><td>0.08</td><td>0.05</td><td>0.04</td><td>0.02</td><td>0.03</td><td>0.06</td><td>0.01</td><td>0.03</td></tr></tbody></table>
Table 6 in Newly discovered species of cheilostomatid Bryozoa from the Miocene of western Kachchh, Gujarat, India
<p><b>Table 6.</b> Measurements in mm of <i>Crepis gurjarensis</i> Guha & Gopikrishna, 2005 (GIS/B 0504 to 0514), Aquitanian, lower Miocene, Kharinadi Formation, western Kachchh, Gujarat, India. Abbreviations: see Material and methods.</p><table><thead><tr><th></th><th><b>Minimum</b></th><th><b>Maximum</b></th><th><b>Mean</b></th><th><b>SD</b></th><th><b>N</b></th></tr></thead><tbody><tr><th>LZ</th><td>0.400</td><td>0.540</td><td>0.484</td><td>± 0.044</td><td>10</td></tr><tr><th>WZ</th><td>0.190</td><td>0.362</td><td>0.284</td><td>± 0.054</td><td>10</td></tr><tr><th>LOp</th><td>0.130</td><td>0.200</td><td>0.161</td><td>± 0.022</td><td>10</td></tr><tr><th>WOp</th><td>0.120</td><td>0.170</td><td>0.143</td><td>± 0.015</td><td>10</td></tr><tr><th>LZ</th><td>0.223</td><td>0.241</td><td>0.233</td><td>± 0.007</td><td>10</td></tr><tr><th>WZ</th><td>0.090</td><td>0.109</td><td>0.102</td><td>± 0.006</td><td>10</td></tr><tr><th>LOr</th><td>0.043</td><td>0.051</td><td>0.048</td><td>± 0.002</td><td>05</td></tr><tr><th>WOr</th><td>0.020</td><td>0.032</td><td>0.028</td><td>± 0.003</td><td>05</td></tr></tbody></table>
TABLE 2 in Beavers and flying squirrels (Rodentia: Castoridae, Pteromyini) from the Late Pliocene of Hambach 11 C, Germany
<p>TABLE 2. — Measurements (in mm) of <i>Trogontherium minus</i> teeth from Hambach 11C.</p><table><tbody><tr><th><b>Museum number</b></th><th><b>Species</b></th><th><b>Dex/Sin</b></th><th><b>Tooth position</b></th><th><b>Length</b></th><th><b>Width</b></th></tr></tbody><tbody><tr><th>HaR-5642-1</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>i</td><td>–</td><td>4.77</td></tr><tr><th>HaR-5642-2</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>p4</td><td>4.05</td><td>3.01</td></tr><tr><th>HaR-5642-3</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>m1</td><td>5.68</td><td>6.27</td></tr><tr><th>HaR-5642-4</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>m2</td><td>5.94</td><td>6.07</td></tr><tr><th>HaR-5643-1</th><td><i>Trogontherium minus</i></td><td>Dex</td><td>P4</td><td>8.24</td><td>8.87</td></tr><tr><th>HaR-5643-2</th><td><i>Trogontherium minus</i></td><td>Dex</td><td>M1</td><td>5.99</td><td>6.21</td></tr><tr><th>HaR-5643-3</th><td><i>Trogontherium minus</i></td><td>Dex</td><td>M2</td><td>5.73</td><td>6.21</td></tr><tr><th>HaR-5644</th><td><i>Trogontherium minus</i></td><td>Dex</td><td>M3</td><td>7.71</td><td>6.05</td></tr><tr><th>HaR-5645</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>P4</td><td>8.31</td><td>9.03</td></tr><tr><th>HaR-5646</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>M1/2</td><td>5.84</td><td>6.19</td></tr><tr><th>HaR-5647</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>M1/2</td><td>6.06</td><td>6.43</td></tr><tr><th>HaR-5648</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>M3</td><td>7.75</td><td>5.97</td></tr><tr><th>HaR-5649</th><td><i>Trogontherium minus</i></td><td>Dex</td><td>P4</td><td>7.2</td><td>8.53</td></tr><tr><th>HaR-5650</th><td><i>Trogontherium minus</i></td><td>Sin</td><td>dP4</td><td>5.18</td><td>5.06</td></tr><tr><th>HaR-5651</th><td><i>Trogontherium minus</i></td><td>Dex</td><td>M3</td><td>5.92</td><td>5.96</td></tr><tr><th>HaR-5652</th><td><i>Trogontherium minus</i></td><td>Dex</td><td>M1/2</td><td>6.08</td><td>5.53</td></tr></tbody></table>
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