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Table 3 in The grass root endophytic fungus Flavomyces fulophazii: An abundant source of tetramic acid and chlorinated azaphilone derivatives
<p><b>Table 3</b> NMR spectroscopic data of <i>E</i> and <i>Z</i> diastereoisomers of vermelhotin (compound <b>5</b>) in chloroform- <i>d</i>, DMSO <i>d</i> 6 and methanol- <i>d</i> 4.</p><table><tbody><tr><th>No. a</th><th>chloroform- <i>d</i></th><th></th><th></th><th></th><th>DMSO <i>d</i> 6</th><th></th><th></th><th></th><th>methanol- <i>d</i> b 4</th><th></th></tr></tbody><tbody><tr><th></th><td><i>δ</i> H (<i>E-</i>)</td><td><i>δ</i> C (<i>E-</i>)</td><td><i>δ</i> H (<i>Z-</i>)</td><td><i>δ</i> C (<i>Z-</i>)</td><td><i>δ</i> H (<i>E-</i>)</td><td><i>δ</i> C (<i>E-</i>)</td><td><i>δ</i> H (<i>Z-</i>)</td><td><i>δ</i> C (<i>Z-</i>)</td><td><i>δ</i> H</td><td><i>δ</i> C</td></tr><tr><th>1 (N)</th><td>5.62, 1H, brs</td><td>–</td><td>5.50, 1H, brs</td><td>–</td><td>7.45 brs, 1H</td><td>–</td><td>7.65 brs, 1H</td><td>–</td><td>–</td><td>–</td></tr><tr><th>2</th><td>–</td><td>171.4</td><td>–</td><td>172.4</td><td>–</td><td>170.9</td><td>–</td><td>170.0</td><td>–</td><td>175.5</td></tr><tr><th>3</th><td>–</td><td>98.1</td><td>–</td><td>97.9</td><td>–</td><td>97.8</td><td>–</td><td>97.7</td><td>–</td><td>98.7</td></tr><tr><th>4</th><td></td><td>192.5</td><td></td><td>194.6</td><td>–</td><td>192.4</td><td>–</td><td>194.8</td><td>–</td><td>195.8</td></tr><tr><th>5</th><td>3.79, s, 2H</td><td>50.4</td><td>3.82, s, 2H</td><td>50.9</td><td>3.58, s, 2H</td><td>49.9</td><td>3.63, s, 2H</td><td>50.4</td><td>3.74, s, 2H</td><td>54.8</td></tr><tr><th>6</th><td>–</td><td>165.4</td><td>–</td><td>166.7</td><td>–</td><td>163.9</td><td>–</td><td>165.3</td><td>–</td><td>162.3</td></tr><tr><th>7</th><td>8.17, d (9.2), 1H</td><td>116.0</td><td>8.18, d (9.2), 1H</td><td>116.5</td><td>8.03, d (9.0), 1H</td><td>115.3</td><td>8.00, d (9.0), 1H</td><td>115.1</td><td>8.10, br, 1H</td><td>116.5</td></tr><tr><th>8</th><td>7.40, dd (9.2, 7.0),</td><td>141.5</td><td>7.41, dd (9.2, 7.0),</td><td>142.0</td><td>7.63, dd (9.0, 7.2),</td><td>142.1</td><td>7.65, dd (9.0, 7.2),</td><td>142.8</td><td>7.67 dd (9.4, 7.2),</td><td>144.7</td></tr><tr><th></th><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td></tr><tr><th>9</th><td>6.29, d (7.0), 1H</td><td>107.5</td><td>6.28, d (7.0), 1H</td><td>107.5</td><td>6.63, d (7.2), 1H</td><td>108.1</td><td>6.63 d, (7.2), 1H</td><td>108.0</td><td>6.60 d (7.2), 1H</td><td>109.9</td></tr><tr><th>10</th><td>–</td><td>158.7</td><td>–</td><td>158.8</td><td>–</td><td>157.3</td><td>–</td><td>157.4</td><td>–</td><td>160.8</td></tr><tr><th>11</th><td>6.17, dq (15.3, 1.5),</td><td>122.1</td><td>6.16, dq (15.3, 1.5),</td><td>122.1</td><td>6.38, dq (15.5, 1.5),</td><td>122.7</td><td>6.38, dq (15.5, 1.5),</td><td>122.8</td><td>6.35 dq (15.5, 1.5),</td><td>123.5</td></tr><tr><th></th><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td></tr><tr><th>12</th><td>7.42, dq (15.3, 7.1),</td><td>138.6</td><td>7.39, dq (15.3, 7.1),</td><td>139.3</td><td>7.18, dq (15.5, 7.0),</td><td>136.1</td><td>7.17 dq (15.5, 7.0),</td><td>136.5</td><td>7.35, br, 1H</td><td>139.5</td></tr><tr><th></th><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td></td><td></td></tr><tr><th>13</th><td>2.01, dd (7.1, 1.5),</td><td>19.0</td><td>1.99, dd (7.1, 1.5),</td><td>18.9</td><td>1.97, dd (7.0, 1.5),</td><td>18.3</td><td>1.95, dd (7.0, 1.5),</td><td>18.4</td><td>1.99 dd (7.2, 1.5),</td><td>18.8</td></tr><tr><th></th><td>3H</td><td></td><td>3H</td><td></td><td>3H</td><td></td><td>3H</td><td></td><td>3H</td><td></td></tr></tbody></table><p><sup>a</sup> Corresponding numbered molecular structure is found in Fig. 2.</p><p><sup>b</sup> Diastereoisomers <i>E</i> and <i>Z</i> vermelhotin could not be separately detected in methanol- <i>d</i>.</p>
Table 2 in Naming Species, A New Paradigm For Crisis Management In Taxonomy: Rapid Journal Validation Of Scientific Names Enhanced With More Complete Descriptions On The Internet
<p><b>Table 2.</b> Current status of the Elateridae in Costa Rica.</p><table><tbody><tr><th>Source</th><th>Tribes Genera</th><th>Species</th></tr></tbody><tbody><tr><th>Literature</th><td>17</td><td>33</td><td>61</td></tr><tr><th>Additional numbers from examined</th><td>0</td><td>9</td><td>218 described</td></tr><tr><th>collections</th><td></td><td></td><td>301 undescribed</td></tr><tr><th>Additional predicted (known to occur elsewhere in Central America)</th><td>0</td><td>?</td><td>?</td></tr><tr><th>Predicted</th><td>17</td><td>42?</td><td>4001</td></tr></tbody></table>
TABLE 8 in Systematics, revisionary taxonomy, and biodiversity of Afrotropical Lithocolletinae (Lepidoptera: Gracillariidae)
<p><b>TABLE 8.</b> Host plants of Lithocolletinae mines recorded from herbarium samples.</p><table><tbody><tr><th><b>Host plant</b></th><th><b>Date</b></th><th><b>Country</b></th><th><b>Details</b></th><th><b>comments on insect sample</b></th></tr></tbody><tbody><tr><th><i>Dombeya kefaensis</i></th><td>29.xi.1995</td><td>Ethiopia</td><td>7°18' N 36°54'E, 2200m Kefa Region, 51 km S of Jimma, Alt. 2200m</td><td>larva</td></tr><tr><th><i>Dombeya rotundifolia</i></th><td>29.vii.1952</td><td>Zimbabwe</td><td></td><td>head of larva</td></tr><tr><th><i>Dombeya torrida</i></th><td>22.xii.1837</td><td>Ethiopia</td><td></td><td>larva</td></tr><tr><th><i>Dombeya wittei</i></th><td>13.vii.1967</td><td>Zambia</td><td>Kitwe</td><td>larva</td></tr><tr><th><i>Grewia picta</i> (<i>= aldabrensis</i>)</th><td>21.ii.1968</td><td>Aldabra</td><td>South Island</td><td>pupa</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>21.ii.1968</td><td>Aldabra</td><td>South Island</td><td>pupa</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>21.ii.1968</td><td>Aldabra</td><td>South Island</td><td>pupa</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>2 pieces of pupal remnants</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>remnant of larva</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>larval head</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>parasite</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>complete larva</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>head of larva</td></tr><tr><th><i>Grewia aldabrensis</i></th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>head of larva</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>head of larva or parasite</td></tr><tr><th><i>Grewia picta</i> (= <i>aldabrensis</i>)</th><td>15.ii.1968</td><td>Aldabra</td><td>Isle Michel</td><td>pupa of parasite</td></tr><tr><th><i>Grewia ferruginea</i></th><td>02.x.1967</td><td>Ethiopia</td><td></td><td>remnant of larva + cocoon of parasite</td></tr><tr><th><i>Grewia pinnatifida</i></th><td>15.ix.1953</td><td>DR Congo</td><td></td><td>mine</td></tr><tr><th><i>Grewia praecox</i></th><td>20.iii.1952</td><td>Zambia</td><td>Lusaka</td><td>Pupa at the moment of eclosion</td></tr><tr><th><i>Grewia similis</i></th><td>1962</td><td>Tanzania</td><td>Kondora District, Salanga Hill</td><td>small second instar larva</td></tr><tr><th><i>Grewia tenax</i></th><td>21.ix.1977</td><td>Niger</td><td>30 km NW d'Agades Kori Szezil. Alt. 520 m</td><td>pupa of parasite</td></tr><tr><th><i>Grewia tenax</i></th><td>21.ix.1977</td><td>Niger</td><td>30 km NW d'Agades Kori Szezil. Alt. 520 m</td><td>remnants of probably parasitic pupa</td></tr><tr><th><i>Grewia tenax</i></th><td>21.ix.1977</td><td>Niger</td><td>30 km NW d'Agades Kori Szezil. Alt. 520 m</td><td>remnants of probably parasitic pupa</td></tr><tr><th><i>Grewia tenax</i></th><td>21.ix.1977</td><td>Niger</td><td>30 km NW d'Agades Kori Szezil. Alt. 520 m</td><td>pressed larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.iii.1995</td><td>Ghana</td><td>07°55'N 02°04'W Brong-Ahato, 300m</td><td>complete larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.iii.1995</td><td>Ghana</td><td>07°55'N 02°04'W Brong-Ahato, 300m</td><td>larva of parasite</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.iii.1995</td><td>Ghana</td><td>07°55'N 02°04'W Brong-Ahato, 300m</td><td>larva squashed together with plant epidermis</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.iii.1995</td><td>Ghana</td><td>07°55'N 02°04'W Brong-Ahato, 300m</td><td>empty pupation camera + remnants of pupa</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.ii.1923</td><td>R.C.A.</td><td>Oubangi-Chari A. E. F.</td><td>larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.ii.1923</td><td>R.C.A.</td><td>Oubangi-Chari, A. E. F.</td><td>larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.ii.1923</td><td>R.C. A.</td><td>Oubangi-Chari A. E. F.</td><td>last instar larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.ii.1923</td><td>R.C.A.</td><td>Oubangi-Chari A. E. F.</td><td>empty mine + remnants of larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>08.ii.1923</td><td>R.C.A.</td><td>Oubangi-Chari A. E. F.</td><td>empty mine + remnants of parasitic pupa</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>20.ii.1921</td><td>R.C.A.</td><td></td><td>last instar larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>20.ii.1921</td><td>R.C.A.</td><td></td><td>young larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>??viii.1932</td><td>DR Congo</td><td>Lualaba, Nyongwe (Maniema)</td><td>last instar larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>??viii.1932</td><td>DR Congo</td><td>Lualaba, Nyongwe (Maniema)</td><td>remnants of larva</td></tr><tr><th><i>Hexalobus crispiflorus</i></th><td>??viii.1932</td><td>DR Congo</td><td>Lualaba, Nyongwe (Maniema)</td><td>complete larva</td></tr><tr><th><i>Pavonia columella</i></th><td>07.viii.1942</td><td>Mozambique</td><td>Massingire, Serra da Morumbala</td><td>head of larva</td></tr><tr><th><i>Rhynchosia luteola var. verdickii</i></th><td>17.iv.1954</td><td>Zimbabwe</td><td>Northern Rhodesia, Chingola</td><td>head of larva</td></tr></tbody></table><p>...... continued on the next page</p>
Supplementary Table S2. DNA polymorphisms in gene sequences of 56 sea buckthorn accessions based on the analysis of whole-genome sequencing data.
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TABLE 1 in Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae)
<p><b>TABLE 1</b> Comparison of characters for distinguishing <i>Deltaya</i> gen.n., <i>Modica</i> gen.n. and related genera.</p><table><tbody><tr><th></th><th><i>Modica gen.n.</i></th><th><i>Emeryus</i></th><th><i>Paryphthimoides</i></th><th><i>Colombeia</i></th><th><i>Scriptor</i></th><th><b><i>Deltaya</i> gen.n.</b></th><th><i>Malaveria</i></th></tr></tbody><tbody><tr><th>Eyes: hair-like setae</th><td>Present</td><td>Absent</td><td>Present</td><td>Present</td><td>Present</td><td>Present</td><td>Present</td></tr><tr><th>DHW pale pupil dots in ocellus in cell Cu2-Cu1</th><td>Visible</td><td>Not visible</td><td>Variably visible</td><td>Variably visible</td><td>Not visible</td><td>Not visible</td><td>Not visible</td></tr><tr><th>VFW: prominent dark brown band (umbra) underlying postdiscal ocelli</th><td>Yes</td><td>No</td><td>Yes, somewhat (except almost absent in <i>P</i>. <i>poltys</i>, <i>P</i>. <i>vestigiata</i>)</td><td>Yes</td><td>Yes</td><td>Yes</td><td>No or weak umbra</td></tr><tr><th>VHW: dark marginal line in tornus</th><td>Thin, not broadening</td><td>Thin, not broadening</td><td>Thin, not broadening (except <i>P</i>. <i>sheba</i>, <i>P</i>. <i>pseudoconfusa</i>)</td><td>Marginal line slightly broader throughout wing</td><td>Broadening</td><td>Broadening</td><td>Thin, not broadening</td></tr><tr><th>VHW: postdiscal ocelli in cells Cu1- M3 and M3-M2</th><td>Double pupils (silver dots or elongate dashes) distinctly ringed with yellow</td><td>Where present, double pupils (silver dots) distinctly ringed with yellow</td><td>Variable across species, either double pupils (silver dots) distinctly ringed with yellow, or single pupil (an elongate silver smudge) indistinctly ringed with orange</td><td>Where present, double pupils (silver dots) distinctly ringed with yellow</td><td>Single pupil (an elongate silver smudge) indistinctly ringed with orange</td><td>Double pupils (silver dots or elongate dashes) distinctly ringed with yellow</td><td>Double pupils (silver dots or elongate dashes) distinctly ringed with yellow</td></tr><tr><th>Male genitalia aedeagus: cornuti</th><td>Variably present</td><td>Present</td><td>Present</td><td>Absent</td><td>Absent</td><td>Present (except in <i>D</i>. <i>andrei</i> and <i>D</i>. <i>probata</i>)</td><td>Absent</td></tr><tr><th>Female genitalia: lamella antevaginalis</th><td>No sclerotized lamella antevaginalis</td><td>Wrinkled, sclerotized lamella antevaginalis</td><td>Sclerotized lamella antevaginalis in some species</td><td>Sclerotized lamella antevaginalis</td><td>No sclerotized lamella antevaginalis</td><td>Sclerotized lamella antevaginalis (except in <i>D</i>. <i>andrei</i> and <i>D</i>. <i>probata</i>)</td><td>Sclerotized ‘spike’-like lamella antevaginalis</td></tr></tbody></table>
TABLE 1 in Phylogenetic position, morphological data, call, and geographic distribution of the elusive treefrog Ololygon skuki (Hylidae: Hylinae: Scinaxini)
<p><b>TABLE 1.</b> Measurements (in mm) of new specimens of <i>Ololygon skuki</i> examined in this study. See Material and Methods for abbreviations.</p><table><tbody><tr><th><b>Measurements</b></th><th><b>Males (<i>n</i> = 3)</b></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td>MHNUFAL 12390</td><td>CFBH 47968</td><td>UFBA 10246</td></tr><tr><th>SVL</th><td>15.3</td><td>14.7</td><td>14.8</td></tr><tr><th>HL</th><td>6.2</td><td>7.4</td><td>5.7</td></tr><tr><th>HW</th><td>5.3</td><td>5.6</td><td>5.2</td></tr><tr><th>IND</th><td>1.3</td><td>1.8</td><td>1.3</td></tr><tr><th>IOD</th><td>1.7</td><td>2.1</td><td>2.0</td></tr><tr><th>ED</th><td>1.8</td><td>1.7</td><td>1.7</td></tr><tr><th>EN</th><td>2.3</td><td>1.8</td><td>1.6</td></tr><tr><th>TD</th><td>0.7</td><td>1.0</td><td>0.7</td></tr><tr><th>TL</th><td>9.3</td><td>9.5</td><td>7.7</td></tr><tr><th>FL</th><td>5.3</td><td>7.3</td><td>5.7</td></tr></tbody></table>
The clinical information of AMI patients is in Supplementary Table I
<p><span>The clinical information of AMI patients is in Supplementary </span><span>Table </span><span>I</span></p>
TABLE 8 in Revisiting the description of Atractoscion macrolepis (Perciformes: Sciaenidae): Another argument for comprehensive taxonomy
<p><b>TABLE 8.</b> Factor loadings, eigenvalues and the variation explained by the first three (of eight) principal components extracted in the Principal Components Analysis of eight transformed otolith variables examining variation among <i>Atractoscion aequidens</i> and <i>A. macrolepis</i>.</p><table><tbody><tr><th>Variable</th><th>Principal Components</th><th></th><th></th></tr></tbody><tbody><tr><th><i>OH’ OL’ OCD’ OrCD’ TOTC’ TOBC’ WC’ OW’</i></th><td>PC1 0.929 0.966 0.573 0.893 0.902 0.976 0.648 0.084</td><td>PC2 -0.068 -0.050 0.136 0.072 -0.071 -0.042 -0.015 0.985</td><td>PC3 -0.235 0.053 0.743 0.071 -0.117 0.036 -0.372 -0.134</td></tr><tr><th>Eigenvalue % Variation Cumulative variation</th><td>5.116 63.95 63.95</td><td>1.007 12.59 76.54</td><td>0.787 9.83 86.37</td></tr></tbody></table>
Table 3 in Temperate grassy wetlands of South Africa: Description, classification and explanatory environmental factors
<p><b>Table 3</b> Indicator species for the broad clusters of temperate grassy wetlands, indicating the Indicator Values and p-values. Only species where the p-value is smaller than 0.05 and the Indicator Value larger than 20 are listed. Alien species are marked with an asterisk.</p><table><tbody><tr><th>Number</th><th>No. of plots</th><th>Dominants</th><th>Where</th><th>Indicator species</th><th>Indicator value</th><th>p - Value</th></tr></tbody><tbody><tr><th>1</th><td>242</td><td>Eleocharis dregeana, Leersia dregeana</td><td>Throughout the country</td><td>Eleocharis dregeana</td><td>47.7</td><td>0.001</td></tr><tr><th>2</th><td>53</td><td><i>Carex acutiformis</i></td><td>Highveld, Kwazulu-Natal</td><td>Carex acutiformis</td><td>75</td><td>0.001</td></tr><tr><th>3</th><td>36</td><td>Aristida junciformis, Helichrysum aureonitens</td><td>Highveld, Kwazulu-Natal</td><td>Fuirena pubescens</td><td>40</td><td>0.001</td></tr><tr><td>Aristida junciformis</td><td>32.7</td><td>0.001</td></tr><tr><td></td><td>Helichrysum aureonitens</td><td>24.3</td><td>0.001</td></tr><tr><th>4</th><td>162</td><td>Cyperus denudatus, Schoenoplectus brachyceras,</td><td>Highveld</td><td><i>Eragrostis curvula</i></td><td>46.7</td><td>0.001</td></tr><tr><td><i>Juncus effusus</i></td><td><i>Hyparrhenia hirta</i></td><td>50.3</td><td>0.001</td></tr><tr><td>Schoenoplectus brachyceras</td><td>88.8</td><td>0.001</td></tr><tr><td>Juncus effusus</td><td>63.8</td><td>0.001</td></tr><tr><td>Cyperus denudatus</td><td>62.3</td><td>0.001</td></tr><tr><th>5</th><td>31</td><td>Eragrostis planiculmis</td><td>Highveld</td><td>Eragrostis planiculmis</td><td>56.7</td><td>0.001</td></tr><tr><th>6</th><td>63</td><td>Arundinella nepalensis, Leucosidea sericea</td><td>Highveld, particularly Drakensberg</td><td>Arundinella nepalensis</td><td>33.7</td><td>0.001</td></tr><tr><td>Leucosidea sericea</td><td>79.7</td><td>0.001</td></tr><tr><td>Searsia dentata</td><td>52.8</td><td>0.001</td></tr><tr><td>Cliffortia nitidula</td><td>36.9</td><td>0.001</td></tr><tr><td>Euclea crispa</td><td>29.2</td><td>0.001</td></tr><tr><th>7</th><td>114</td><td><i>Hemarthria altissima</i>, Cyperus marginatus,</td><td>Mostly Highveld</td><td>Hemarthria altissima</td><td>37.6</td><td>0.001</td></tr><tr><td><i>Paspalum dilatatum</i></td><td>Cyperus marginatus</td><td>63.8</td><td>0.001</td></tr><tr><td><i>Cynodon dactylon</i></td><td>30.6</td><td>0.001</td></tr><tr><td><i>Plantago lanceolata</i></td><td>29.7</td><td>0.001</td></tr><tr><td>Paspalum dilatatum</td><td>26.4</td><td>0.001</td></tr><tr><td><i>Trifolium repens</i></td><td>26.2</td><td>0.001</td></tr><tr><th>8</th><td>65</td><td><i>Themeda triandra</i></td><td>Highveld</td><td>Themeda triandra</td><td>52.4</td><td>0.001</td></tr><tr><th>9</th><td>77</td><td>Cyperus fastigiatus</td><td>Throughout the country</td><td>Cyperus fastigiatus</td><td>62.8</td><td>0.001</td></tr><tr><th>10</th><td>136</td><td><i>Imperata cylindrica</i></td><td>Throughout the country</td><td>Imperata cylindrica</td><td>41.1</td><td>0.001</td></tr><tr><td>Senecio achilleifolius</td><td>54.2</td><td>0.001</td></tr><tr><td>Pulicaria scabra</td><td>47.3</td><td>0.001</td></tr><tr><td>Andropogon eucomus</td><td>42.2</td><td>0.001</td></tr><tr><td><i>Fimbristylis ferruginea</i></td><td>41.6</td><td>0.001</td></tr><tr><td><i>Paspalum urvillei</i></td><td>34.9</td><td>0.001</td></tr><tr><td>Pycreus betschuanus</td><td>26.8</td><td>0.001</td></tr><tr><td>Chamaecrista stricta</td><td>26.4</td><td>0.001</td></tr><tr><td>Kyllinga alba</td><td>31.8</td><td>0.001</td></tr><tr><td>Miscanthus junceus</td><td>28.9</td><td>0.001</td></tr><tr><td>Phymaspermum athanasoides</td><td>26.6</td><td>0.001</td></tr><tr><td>Wahlenbergia undulata</td><td>26.4</td><td>0.001</td></tr><tr><th>11</th><td>138</td><td><i>Eragrostis plana</i></td><td>Throughout the country</td><td>Eragrostis plana</td><td>29.8</td><td>0.001</td></tr><tr><th>12</th><td>107</td><td>Typha capensis</td><td>Throughout the country</td><td>Typha capensis</td><td>51.9</td><td>0.001</td></tr><tr><th>13</th><td>90</td><td><i>Phragmites australis</i></td><td>Throughout the country</td><td>Phragmites australis</td><td>39.5</td><td>0.001</td></tr></tbody></table>
Table 3 in Ultrastructure of somatic embryo development and plant propagation for Lachenalia montana
<p><b>Table 3</b> Enhancement of somatic embryos (SEs) and germination frequency in cell suspension culture from friable embryogenic callus (FEC) of L. montana.</p><table><tbody><tr><th>Sucrose (g L <i>−</i> 1) + PGR (μM) in solid MS medium</th><th>PGR (μM) in liquid MS medium</th><th>Liquid MS medium (MSL)</th><th>Number of SEs/SCV developmental stage</th><th>Germination (%)</th></tr></tbody><tbody><tr><th>6 weeks of culture</th><td>4 weeks of culture</td><td>2 weeks of culture</td><td>Globular</td><td>Different stages of embryo*</td><td></td></tr><tr><th>35 + 10 2,4-D + 2 TDZ</th><td>0.5 2,4-D + 1 BA</td><td>MSL</td><td>17.6 b</td><td>9.4 c</td><td>23.0 de</td></tr><tr><td>0.5 2,4-D + 1 <i>m</i> TR</td><td>MSL</td><td>13.2 cd</td><td>8.0 cd</td><td>22.6 e</td></tr><tr><td>0.5 2,4-D + 1 TDZ</td><td>MSL</td><td>26.0 a</td><td>19.4 a</td><td>24.2 d</td></tr><tr><td>1 2,4-D + 1 BA</td><td>MSL</td><td>10.6 e</td><td>7.4 de</td><td>24.4 d</td></tr><tr><td>1 2,4-D + 1 <i>m</i> TR</td><td>MSL</td><td>9.8 ef</td><td>6.2 e</td><td>23.7 de</td></tr><tr><td>1 2,4-D + 1 TDZ</td><td>MSL</td><td>15.4 c</td><td>9.6 c</td><td>32.0 b</td></tr><tr><td>1 2,4-D + 2 BA</td><td>MSL</td><td>7.0 gh</td><td>6.6 e</td><td>22.1 e</td></tr><tr><td>1 2,4-D + 2 <i>m</i> TR</td><td>MSL</td><td>5.6 h</td><td>7.8 de</td><td>26.9 c</td></tr><tr><td>1 2,4-D + 2 TDZ</td><td>MSL</td><td>9.0 ef</td><td>11.8 b</td><td>34.7 a</td></tr></tbody></table><p>PGR = Plant growth regulator. <sub>MSL</sub> = Liquid MS medium. SEs = Somatic embryos. SCV = Settled cell volume. *Different stages of embryo = pear-shaped, early torpedo-shaped, torpedoshaped and cotyledonary-stage embryos. Values with the means derived from 5 replicate (each 500 mg FEC) with 1000 μL SCV of embryogenic suspension cells per replicate.Mean values followed by same letters in each column are not significantly different according to the Duncan's multiple range test at 5% level.</p>
Table 1 in Gene identification using RNA-seq in two sweetpotato genotypes and the use of mining to analyze carotenoid biosynthesis
<p><b>Table 1</b> Length distribution of the assembled transcripts and unigenes.</p><table><tbody><tr><th>Nucleotides length (bp)</th><th>Transcripts</th><th>Unigenes</th></tr></tbody><tbody><tr><th>200–500 bp</th><td>90,099</td><td>67,643</td></tr><tr><th>500–1000 bp</th><td>38,799</td><td>21,181</td></tr><tr><th>1000–2000 bp</th><td>30,015</td><td>13,149</td></tr><tr><th>>2000 bp</th><td>17,254</td><td>7428</td></tr><tr><th>Total</th><td>176,167</td><td>109,401</td></tr><tr><th>Min length</th><td>201</td><td>201</td></tr><tr><th>Mean length</th><td>847</td><td>694</td></tr><tr><th>Median length</th><td>486</td><td>385</td></tr><tr><th>Max length</th><td>15,618</td><td>15,618</td></tr><tr><th>N50</th><td>1430</td><td>1127</td></tr><tr><th>N90</th><td>333</td><td>277</td></tr><tr><th>Total nucleotides</th><td>149,175,171</td><td>75,954,853</td></tr></tbody></table>
TABLE 1 in A new genus for the Blackfin Sucker, Thoburnia atripinnis (Cypriniformes: Catostomidae)
<p><b>TABLE 1.</b> Morphometrics of <i>Vexillichthys</i> <b>n. gen.</b> <i>atripinnis</i>. N=24.</p><table><tbody><tr><th></th><th><b>Average</b></th><th><b>SD</b></th><th><b>Minimum</b></th><th><b>Maximum</b></th></tr></tbody><tbody><tr><th>SL (mm)</th><td>110.8</td><td></td><td>71.6</td><td>133.7</td></tr><tr><th><i>%SL</i></th></tr><tr><th>Body Depth</th><td>18.8</td><td>1.8</td><td>16.1</td><td>26.1</td></tr><tr><th>Caudal Peduncle Depth</th><td>9.5</td><td>0.8</td><td>8.5</td><td>12.4</td></tr><tr><th>Caudal Peduncle Length</th><td>18.4</td><td>1.6</td><td>16.1</td><td>24.0</td></tr><tr><th>Predorsal Length</th><td>46.5</td><td>3.2</td><td>43.6</td><td>60.6</td></tr><tr><th>Dorsal-fin Base Length</th><td>13.5</td><td>1.7</td><td>11.7</td><td>19.1</td></tr><tr><th>Anal-fin Base Length</th><td>8.9</td><td>1.4</td><td>7.3</td><td>13.8</td></tr><tr><th>Dorsal Fin Height</th><td>16.7</td><td>1.7</td><td>14.2</td><td>21.1</td></tr><tr><th>Anal Fin Height</th><td>22.5</td><td>2.9</td><td>19.3</td><td>33.7</td></tr><tr><th>Depressed Dorsal Fin Length</th><td>23.2</td><td>2.9</td><td>20.0</td><td>33.4</td></tr><tr><th>Longest Anal Ray Length</th><td>19.2</td><td>2.1</td><td>16.6</td><td>27.2</td></tr><tr><th>Head Length (HL)</th><td>20.1</td><td>1.4</td><td>18.9</td><td>26.0</td></tr><tr><th><i>%HL</i></th></tr><tr><th>Head Depth</th><td>69.6</td><td>3.1</td><td>64.8</td><td>77.7</td></tr><tr><th>Snout Length</th><td>46.1</td><td>2.6</td><td>41.9</td><td>52.4</td></tr><tr><th>Postorbital Head Length</th><td>37.5</td><td>4.0</td><td>29.7</td><td>46.7</td></tr><tr><th>Orbit to Angle of Preopercle Length</th><td>43.7</td><td>3.5</td><td>40.1</td><td>54.4</td></tr><tr><th>Interorbital Width</th><td>45.6</td><td>3.0</td><td>39.6</td><td>52.2</td></tr><tr><th>Orbit Length</th><td>29.8</td><td>1.8</td><td>25.7</td><td>33.2</td></tr><tr><th>Upper Jaw Length</th><td>30.9</td><td>2.8</td><td>27.1</td><td>40.2</td></tr><tr><th>Mandible Length</th><td>19.1</td><td>1.8</td><td>15.6</td><td>22.4</td></tr><tr><th>Gape Width</th><td>32.0</td><td>1.9</td><td>27.7</td><td>35.9</td></tr></tbody></table>
Table 4 in Phytoconstituents from Vernonia glaberrima Welw. Ex O. Hoffm. leaves and their cytotoxic activities on a panel of human cancer cell lines
<p><b>Table 4</b> Docking scores of 5-methylcoumarin-4-β- glucoside and 4-hydroxy-5-methylcoumarin on carbonic anhydrase IX (CAIX) (PDB ID 3IAI).</p><table><tbody><tr><th></th><th>Name</th><th>Free binding energy (kcal/mol)</th><th>Estimated inhibition constant (Ki)</th></tr></tbody><tbody><tr><th>1</th><td>5-Methylcoumarin-4-β- glucoside</td><td><i>−</i> 6.97</td><td>7.78 μM</td></tr><tr><th>2</th><td>4-Hydroxy-5-methylcoumarin</td><td><i>−</i> 5.70</td><td>66.17 μM</td></tr><tr><th>3</th><td>Co-crystallized ligand</td><td><i>−</i> 6.01</td><td>39.32 μM</td></tr></tbody></table>
Table 6 in Phylogeny, evolution, and classification of the ant genus Lasius, the tribe Lasiini and the subfamily Formicinae (Hymenoptera: Formicidae)
<p><b>Table 6.</b> Results of ANOVA tests on alternative ancestral state estimation models.</p><table><tbody><tr><th></th><th>Divergence dating</th><th></th><th></th><th></th><th></th><th></th><th></th><th></th><th>Biogeography reconstruction</th><th></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td>FBD IGRclock</td><td></td><td>FBDTK02 clock</td><td></td><td>UniformIGRclock</td><td>Uniform TK 02 clock</td><td></td><td>DEC (lnL − 136.77)</td><td>DIVALIKE (lnL − 132.24)</td><td>BAYAREALIKE (lnL − 150.98)</td></tr><tr><th>Node</th><td>Meanage(95 % HPD)</td><td>PP</td><td>Meanage(95 % HPD)</td><td>PP</td><td>Mean age(95 % HPD)</td><td>PP</td><td>Mean age (95 % HPD)</td><td>PP</td><td>Range</td><td>Likelihood</td><td>Range</td><td>Likelihood</td><td>Range</td><td>Likelihood</td></tr><tr><th>LasiiniCore LasiiniMetalasius + Prenolepis g. grp.</th><td>70.0 (57.6 –82.7) 62.3 (51.2 –72.9) 51.1 (42.2 –60.2)</td><td>0.990.940.99</td><td>97.2 (89.6 – 106.0) 88.6 (79.8 – 97.8) 71.0 (60.8 – 81.9)</td><td>0.910.641.00</td><td>80.8(68.6 – 91.8) 72.5(59.0 – 85.4) 59.9(48.7 –72.8)</td><td>0.96 0.94 0.99</td><td>100.0 (90.9 – 112.3) 92.0 (83.5 – 102.2) 75.6 (65.1 – 86.5)</td><td>0.94 0.49 1.00</td><td>PI P P</td><td>0.33 0.42 0.40</td><td>PI P P</td><td>0.37 0.56 0.53</td><td>PI PI PI</td><td>0.43 0.43 0.48</td></tr><tr><th><i>Prenolepis</i> g. grp. <i>Lasius</i> g. grp. Crown Lasiusniger clade <i>flavus</i> clade <i>Myrmecocystus</i></th><td>39.0 (36.5 –50.9) 24.9 (18.0 – 33.0) 21.9 (15.3 – 28.6) 15.8 (10.0 – 21.6) 15.7 (10.4 – 21.0) 14.6 (7.3 – 21.5)</td><td><b>0.471.000.771.001.001.00</b></td><td><b>53.1 (43.6 – 62.6) 67.9 (54.9 – 81.6) 63.7 (52.4 – 75.1) 53.2 (41.2 – 65.3) 49.1 (36.7 – 61.8) 47.9 (33.5 – 63.1)</b></td><td><b>1.000.990.630.701.001.00</b></td><td><b>50.9(40.8 – 61.3) 31.1(22.4 – 40.5) <i>27.3(19.4 – 35.6)</i> 20.0(12.7 – 27.7) 19.7(13.2– 26.8)</b> 17.8(8.9 – 26.9)</td><td>1.00 0.99 0.73 1.00 1.00 1.00</td><td>57.0 (48.2 – 66.5) 73.7 (61.9 – 88.3) 64.3 (58.4 – 82.2) 60.6 (46.1 – 73.0) 55.9 (41.1 – 69.4) 55.8 (40.0 – 69.8)</td><td>1.00 0.99 0.71 0.56 1.00 1.00</td><td>PI NaP P P Na Na</td><td>0.42 0.53 0.72 0.87 0.71 0.87</td><td>PI Na P P Na Na</td><td>0.50 0.55 0.71 0.99 0.90 0.97</td><td><b>PI NaP NaP NaP NaP Na</b></td><td><b><b>0.64 0.84 0.87 0.62</b> 0.91</b> 0.53</td></tr></tbody></table>
Table 3 in Phytoconstituents from Vernonia glaberrima Welw. Ex O. Hoffm. leaves and their cytotoxic activities on a panel of human cancer cell lines
<p><b>Table 3</b> Docking result for lupeol on CDK2 (PDB ID 2DUV).</p><table><tbody><tr><th></th><th>Name</th><th>Free binding energy (kcal/mol)</th><th>Estimated inhibition constant (Ki)</th></tr></tbody><tbody><tr><th>1</th><td>Lupeol</td><td><i>−</i> 11.06</td><td>7.82 nM</td></tr><tr><th>2</th><td>Co-crystallized</td><td><i>−</i> 11.08</td><td>7.57 nM</td></tr></tbody></table>
TABLE 3 in Psammobiont halacarid mites (Acari: Halacaridae) from Türkiye: description of two new species of the genus Atelopsalis Trouessart, 1896 and Scaptognathus Trouessart, 1889 and two new records
<p><b>TABLE 3.</b> Summary of data on stations, species identities.</p><table><tbody><tr><th><b>Station</b></th><th><b>St. 1</b></th><th><b>St. 2</b></th><th><b>St. 3</b></th></tr></tbody><tbody><tr><th><b>Date</b></th><td>Oct. 2015</td><td>10 Jun. 2016</td><td>3 July 2018</td></tr><tr><th><b>Locality</b></th><td>Kaş, Antalya</td><td>Örnekköy, Antalya</td><td>Kundu, Antalya</td></tr><tr><th><b>Position</b></th><td>36.157583,29.630333</td><td>36.846944,30.805000</td><td>36.849361,30.839000</td></tr><tr><th><b>Depth</b></th><td>30 m</td><td>- 0.5 m; 3 m</td><td>3 m</td></tr><tr><th><b>Substrate</b></th><td>well sorted soft sand</td><td>well sorted medium sand</td><td>well sorted soft sand</td></tr><tr><th><b>Species</b></th><td><i>A. mediterranea</i> <b>sp. nov.</b></td><td><i>A. delamarei</i>; <i>A. anomalus</i></td><td><i>S. antalyensis</i> <b>sp. nov.</b></td></tr><tr><th><b>Specimens, types and catalogue numbers</b></th><td>1♀ 5♂♂ 1DN FDHAL-24/87-91</td><td>6♀♀ 2♂♂1DN FDHAL-24/78-81; 1♀ 1♂ FDHAL-24/82,83</td><td>1♀ 1♂ FDHAL-24/106,107</td></tr></tbody></table>
Table 4 in Phylogeny, evolution, and classification of the ant genus Lasius, the tribe Lasiini and the subfamily Formicinae (Hymenoptera: Formicidae)
<p><b>Table 4.</b> Bayes Factor results, testing alternative placements of <i>Metalasius</i> and the monophyly of the subgenera using the Lasiini _55t matrix.</p><table><tbody><tr><th>SS</th><th>Marg. log</th><th>Marg. log</th><th></th></tr></tbody><tbody><tr><th>run</th><td>likelihood H0</td><td>likelihood H1</td><td>2lne(B10)</td></tr><tr><th></th><td><i>Metalasius</i> +</td><td><i>Metalasius</i> +</td><td></td></tr><tr><th></th><td><i>Lasius</i> g. g.</td><td><i>Prenolepis</i> g. g.</td><td></td></tr><tr><th>1</th><td>−29 156.21</td><td>−29 092.2</td><td></td></tr><tr><th>2</th><td>−29 153.15</td><td>−29 094.4</td><td></td></tr><tr><th>Mean</th><td>−29 153.79</td><td><b>−29 092.79</b></td><td>−122</td></tr><tr><th>SS</th><td>Marg. log</td><td>Marg. log</td><td></td></tr><tr><th>run</th><td>likelihood H0</td><td>likelihood H1</td><td>2lne(B10)</td></tr><tr><th></th><td><i>Lasius</i> monophyletic</td><td><i>Lasius</i> paraphyletic</td><td></td></tr><tr><th>1</th><td>−29 068.73</td><td>−29 072.46</td><td></td></tr><tr><th>2</th><td>−29 068.86</td><td>−29 072.04</td><td></td></tr><tr><th>Mean</th><td><b>−29 068.79</b></td><td>−29 072.23</td><td>6.88</td></tr><tr><th>SS</th><td>Marg. log</td><td>Marg. log</td><td></td></tr><tr><th>run</th><td>likelihood H0</td><td>likelihood H1</td><td>2lne(B10)</td></tr><tr><th></th><td><i>Lasius</i> s. str.</td><td><i>Lasius</i> s. str.</td><td></td></tr><tr><th></th><td>monophyletic</td><td>paraphyletic</td><td></td></tr><tr><th>1</th><td>−29 092.4</td><td>−29 057.37</td><td></td></tr><tr><th>2</th><td>−29 094.02</td><td>−29 058.11</td><td></td></tr><tr><th>Mean</th><td>−29 092.91</td><td><b>−29 057.67</b></td><td>−70.48</td></tr><tr><th>SS</th><td>Marg. log</td><td>Marg. log</td><td></td></tr><tr><th>run</th><td>likelihood H0</td><td>likelihood H1</td><td>2lne(B10)</td></tr><tr><th></th><td><i>Cautolasius</i></td><td><i>Cautolasius</i></td><td></td></tr><tr><th></th><td>monophyletic</td><td>paraphyletic</td><td></td></tr><tr><th>1</th><td>−29 063.91</td><td>−29 054.38</td><td></td></tr><tr><th>2</th><td>−29 064.12</td><td>−29 054.21</td><td></td></tr><tr><th>Mean</th><td>−29 064.01</td><td><b>−29 054.29</b></td><td>−19.44</td></tr><tr><th>SS</th><td>Marg. log</td><td>Marg. log</td><td></td></tr><tr><th>run</th><td>likelihood H0</td><td>likelihood H1</td><td>2lne(B10)</td></tr><tr><th></th><td><i>Chthonolasius</i></td><td><i>Chthonolasius</i></td><td></td></tr><tr><th></th><td>monophyletic</td><td>polyphyletic</td><td></td></tr><tr><th>1</th><td>−29 100.32</td><td>−29 047.78</td><td></td></tr><tr><th>2</th><td>−29 099.17</td><td>−29 046.75</td><td></td></tr><tr><th>Mean</th><td>−29 099.59</td><td><b>−29 047.13</b></td><td>−104.92</td></tr></tbody></table><p>The mean value for the best-supported hypothesis for each comparison is bolded.</p>
TABLE 2 in Investigation of the distribution patterns in moinids (Crustacea: Cladocera: Moinidae) forming ephippia with two resting eggs
<p><b>TABLE 2</b>. Data matrix of 26 morphological characters used in cladistic analysis.</p><table><tbody><tr><th><b>Taxon</b></th><th><b>1</b></th><th><b>2</b></th><th><b>3</b></th><th><b>4</b></th><th><b>5</b></th><th><b>6</b></th><th><b>7</b></th><th><b>8</b></th><th><b>9</b></th><th><b>10</b></th><th><b>11</b></th><th><b>12</b></th><th><b>13</b></th><th><b>14</b></th><th><b>15</b></th><th><b>16</b></th><th><b>17</b></th><th><b>18</b></th><th><b>19</b></th><th><b>20</b></th><th><b>21</b></th><th><b>22</b></th><th><b>23</b></th><th><b>24</b></th><th><b>25</b></th><th><b>26</b></th></tr></tbody><tbody><tr><th><i>australiensis</i></th><td>1</td><td>0</td><td>1</td><td>1</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td><td>2</td><td>0</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>0</td><td>2</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>tenuicornis</i></th><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td><td>2</td><td>0</td><td>9</td><td>1</td><td>1</td><td>1</td><td>1</td><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>macrocopa</i></th><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>2</td><td>0</td><td>1</td><td>2</td><td>1</td><td>1</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>americana</i></th><td>1</td><td>0</td><td>1</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>2</td><td>0</td><td>1</td><td>2</td><td>1</td><td>1</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>belli</i></th><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>kazsabi</i></th><td>1</td><td>0</td><td>1</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>lipini</i></th><td>1</td><td>0</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>9</td><td>9</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>9</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>ephemeralis</i></th><td>1</td><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>9</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td></tr><tr><th><i>hutchinsoni</i></th><td>1</td><td>0</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>9</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>9</td><td>1</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>1</td><td>1</td><td>0</td><td>0</td></tr><tr><th><i>wierzejskii</i></th><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>2</td><td>0</td><td>0</td><td>0</td><td>2</td><td>0</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>0</td><td>1</td><td>1</td><td>1</td><td>0</td><td>0</td></tr><tr><th><i>brachiata</i></th><td>0</td><td>0</td><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td></tr><tr><th><i>micrura</i></th><td>0</td><td>0</td><td>1</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>1</td><td>2</td><td>0</td><td>0</td><td>0</td><td>2</td><td>0</td><td>0</td><td>0</td><td>2</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td></tr><tr><th><i>macleayi</i></th><td>0</td><td>1</td><td>0</td><td>0</td><td>1</td><td>2</td><td>1</td><td>0</td><td>0</td><td>1</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td><td>2</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td></tr></tbody></table>
Table 3 in Acute toxicity and antiproliferative and procoagulant activities of fractions derived from Thymus satureioides of the Moroccan High Atlas
<p><b>Table 3</b> Antioxidant activity of CE and organic fractions from of T. satureioides.</p><table><tbody><tr><th>Extract</th><th>FRAP (mmol Trolox/g DR)</th><th>Radical scavenging activity [IC50 (mg/mL DR)]</th></tr></tbody><tbody><tr><th>Crude extract</th><td>41.41 ± 4.55</td><td>0.44 ± 0.06*</td></tr><tr><th>Dichloromethane fraction</th><td>33.48 ± 0.08*</td><td>0.48 ± 0.05</td></tr><tr><th>Ethyl acetate fraction</th><td>82.69 ± 2.29**</td><td>0.33 ± 0.02**</td></tr><tr><th>Methanol fraction</th><td>55.99 ± 2.21*</td><td>0.71 ± 0.09**</td></tr><tr><th>Aqueous fraction</th><td>25.46 ± 2.71**</td><td>0.85 ± 0.06**</td></tr><tr><th>Trolox</th><td>44.33 ± 7.55</td><td>0.51 ± 0.01</td></tr></tbody></table>
TABLE 1 in Dzihunia pseudoamudarjensis, a new nemacheilid loach from the Syr Darya drainage (Teleostei: Nemacheilidae)
<p><b>TABLE 1.</b> Morphometric data of <i>Dzihunia pseudoamudarjensis</i> (holotype SWU08122023001 and paratypes SWU 08122023002, n=10; BSFC 0073, n=6; and ZIN 57058, n=2).</p><table><tbody><tr><th></th><th><b>Holotype</b></th><th><b>min</b></th><th><b>Holotype & Paratypes max mean</b></th><th><b>SD</b></th></tr></tbody><tbody><tr><th>Total length (mm)</th><td>116.7</td><td>71.2</td><td>128.2</td><td>100.1</td><td></td></tr><tr><th>Standard length (mm)</th><td>95.9</td><td>58.4</td><td>107.2</td><td>82.7</td><td></td></tr><tr><th><b>In percent of standard length</b></th></tr><tr><th>Head length</th><td>22.1</td><td>19.2</td><td>22.8</td><td>21.1</td><td>1.0</td></tr><tr><th>Body depth at dorsal-fin origin</th><td>14.7</td><td>12.9</td><td>15.3</td><td>14.0</td><td>0.6</td></tr><tr><th>Body width at dorsal-fin origin</th><td>12.2</td><td>10.5</td><td>12.6</td><td>11.4</td><td>0.5</td></tr><tr><th>Predorsal length</th><td>50.3</td><td>48.3</td><td>52.6</td><td>50.6</td><td>1.2</td></tr><tr><th>Postdorsal length</th><td>40.3</td><td>36.7</td><td>41.8</td><td>39.8</td><td>1.3</td></tr><tr><th>Prepelvic length</th><td>47.2</td><td>46.1</td><td>49.4</td><td>47.6</td><td>0.9</td></tr><tr><th>Preanal length</th><td>69.1</td><td>67.0</td><td>70.9</td><td>69.3</td><td>1.1</td></tr><tr><th>Dorsal-fin depth</th><td>15.4</td><td>13.1</td><td>16.6</td><td>14.7</td><td>1.0</td></tr><tr><th>Dorsal-fin base length</th><td>12.7</td><td>11.0</td><td>14.2</td><td>12.7</td><td>0.7</td></tr><tr><th>Anal-fin height</th><td>14.7</td><td>12.7</td><td>16.6</td><td>14.0</td><td>1.1</td></tr><tr><th>Anal-fin base length</th><td>9.0</td><td>7.6</td><td>9.6</td><td>8.4</td><td>0.5</td></tr><tr><th>Pectoral-fin length</th><td>17.2</td><td>14.9</td><td>18.6</td><td>16.8</td><td>1.2</td></tr><tr><th>Pelvic-fin length</th><td>14.3</td><td>12.5</td><td>17.0</td><td>14.3</td><td>1.3</td></tr><tr><th>Caudal peduncle length</th><td>22.4</td><td>20.6</td><td>23.6</td><td>22.3</td><td>0.9</td></tr><tr><th>Caudal peduncle depth</th><td>5.4</td><td>4.9</td><td>6.0</td><td>5.5</td><td>0.3</td></tr><tr><th>Pectoral-pelvic fins origins distance</th><td>28.4</td><td>23.6</td><td>30.2</td><td>28.7</td><td>1.4</td></tr><tr><th>Pelvic-anal fins origins distance</th><td>21.7</td><td>19.8</td><td>23.7</td><td>21.7</td><td>1.0</td></tr><tr><th>Vent-anal fin origin distance</th><td>3.7</td><td>2.7</td><td>4.6</td><td>3.5</td><td>0.5</td></tr><tr><th>Caudal peduncle length/depth</th><td>4.2</td><td>3.5</td><td>4.5</td><td>4.1</td><td>0.3</td></tr><tr><th><b>In percent of head length</b></th></tr><tr><th>Head depth at nape</th><td>54.4</td><td>51.3</td><td>58.0</td><td>54.0</td><td>2.0</td></tr><tr><th>Head depth at eye</th><td>45.5</td><td>42.0</td><td>49.8</td><td>45.3</td><td>2.1</td></tr><tr><th>Maximum head width</th><td>64.2</td><td>60.8</td><td>72.0</td><td>66.1</td><td>3.1</td></tr><tr><th>Snout length</th><td>50.2</td><td>43.4</td><td>52.3</td><td>46.4</td><td>2.1</td></tr><tr><th>Eye diameter</th><td>9.8</td><td>9.2</td><td>13.2</td><td>10.8</td><td>1.1</td></tr><tr><th>Interorbital width</th><td>31.2</td><td>27.8</td><td>35.2</td><td>30.3</td><td>1.7</td></tr><tr><th>Postorbital length</th><td>45.0</td><td>43.9</td><td>49.6</td><td>47.5</td><td>1.7</td></tr><tr><th>Maxillary barbel length</th><td>30.6</td><td>24.2</td><td>34.6</td><td>29.3</td><td>3.3</td></tr><tr><th>Inner premaxillary barbel length</th><td>22.2</td><td>20.3</td><td>29.5</td><td>24.3</td><td>2.4</td></tr><tr><th>Outer premaxillary barbel length</th><td>33.5</td><td>29.3</td><td>41.6</td><td>34.7</td><td>3.8</td></tr></tbody></table><p>......continued on the next page</p>
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