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zenodo28/100

Table 2 in Antioxidant and anticholinesterase potential of Ferulago cassia with farther bio-guided isolation of active coumarin constituents *

<p><b>Table 2</b> Antioxidant activities of the samples from <i>Ferulago cassia</i> in TBA test.</p><table><tbody><tr><th>Tested samples</th><th>IC50 values (&mu;g/mL) &plusmn; SD*</th></tr></tbody><tbody><tr><th></th><td>Aerial part</td><td>Root</td><td>Flower</td><td>Fruit</td></tr><tr><th>MeOH</th><td>195.42 &plusmn; 4.25</td><td>92.21 &plusmn; 3.44</td><td>178.31 &plusmn; 4.33</td><td>155.67 &plusmn; 3.66</td></tr><tr><th>Hexane</th><td>500&gt;</td><td>500&gt;</td><td>500&gt;</td><td>500&gt;</td></tr><tr><th>CH2Cl2</th><td>85.66 &plusmn; 5.02</td><td>43.10 &plusmn; 2.23</td><td>101.13 &plusmn; 2.34</td><td>52.45 &plusmn; 1.67</td></tr><tr><th>EtOAc</th><td>145.65 &plusmn; 2.57</td><td>112.10 &plusmn; 3.47</td><td>181.21 &plusmn; 1.06</td><td>94.91 &plusmn; 3.41</td></tr><tr><th>BuOH</th><td>345.21 &plusmn; 4.30</td><td>471.31 &plusmn; 4.91</td><td>383.23 &plusmn; 2.43</td><td>276.51 &plusmn; 1.66</td></tr><tr><th>Aqueous residue</th><td>500&gt;</td><td>500&gt;</td><td>500&gt;</td><td>500&gt;</td></tr><tr><th>Lyophilized aqueous</th><td>500&gt;</td><td>464.89 &plusmn; 2.09</td><td>489 &plusmn; 3.28</td><td>356 &plusmn; 1.93</td></tr><tr><th>Peucedanol</th><td>18.12 &plusmn; 2.80</td><td></td><td></td><td></td></tr><tr><th>Suberosin</th><td>23.54 &plusmn; 2.43</td><td></td><td></td><td></td></tr><tr><th>Grandivitinol</th><td>61.11 &plusmn; 4.23</td><td></td><td></td><td></td></tr><tr><th>Umbelliferone</th><td>79.53 &plusmn; 3.98</td><td></td><td></td><td></td></tr><tr><th>Chlorogenic acid</th><td>12.98 &plusmn; 4.89</td><td></td><td></td><td></td></tr><tr><th>Propyl gallate</th><td>3.44 &plusmn; 2.05</td><td></td><td></td><td></td></tr><tr><th>Rutin</th><td>9.65 &plusmn; 3.09</td><td></td><td></td><td></td></tr></tbody></table><p>* Standard deviation.</p>

opennotspecifiedMar 2019View details →
zenodo28/100

Table 4 in First insights into past biodiversity of giraffes based on mitochondrial sequences from museum specimens

<p><b>Table 4.</b> Minimum and maximum pairwise distances (in %), as well as mean distance (between brackets), calculated using the nuDNA-78T dataset both within and between haplogroups (Fig. 3). <b>Boldface</b> = maximal intrapopulational variation.</p><table><tbody><tr><th>Taxa</th><th><b>I</b>.</th><th><b>II</b>.</th><th><b>III</b>.</th><th><b>IV</b>.</th><th><b>V</b>.</th><th><b>VI</b>.</th><th><b>VII</b>.</th><th><b>VIII</b>.</th><th><b>IX</b>.</th><th></th></tr></tbody><tbody><tr><th><b>I</b>. Niger</th><td><b>0</b>. <b>09</b></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>II</b>. Kordofan I</th><td>0.03 &ndash; 0.11 (0.06)</td><td><b>0</b>. <b>04</b></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>III</b>. Kordofan II</th><td>0.08 &ndash; 0.12 (0.1)</td><td>0.04 &ndash; 0.05 (0.04)</td><td><b>0</b></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>IV</b>. Rothschild</th><td>0.04 &ndash; 0.21 (0.08)</td><td>0.02 &ndash; 0.17 (0.07)</td><td>0.05 &ndash; 0.2 (0.09)</td><td><b>0</b>. <b>2</b></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>V</b>. Reticulated I</th><td>0.05 &ndash; 0.27 (0.15)</td><td>0.02 &ndash; 0.21 (0.14)</td><td>0.08 &ndash; 0.23 (0.18)</td><td>0 &ndash; 0.25 (0.13)</td><td><b>0</b>. <b>12</b></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>VI</b>. Masai I</th><td>0.40 &ndash; 0.47 (0.44)</td><td>0.40 &ndash; 0.49 (0.44)</td><td>0.46 &ndash; 0.48 (0.47)</td><td>0.38 &ndash; 0.5 (0.44)</td><td>0.32 &ndash; 0.47 (0.41)</td><td><b>0</b></td><td></td><td></td><td></td><td></td></tr><tr><th><b>VII</b>. Masai II</th><td>0.4 &ndash; 0.46 (0.44)</td><td>0.44 &ndash; 0.47 (0.45)</td><td>0.46 &ndash; 0.46 (0.46)</td><td>0.38 &ndash; 0.49 (0.44)</td><td>0.32 &ndash; 0.46 (0.40)</td><td>0.02 &ndash; 0.06 (0.04)</td><td><b>0</b>. <b>04</b></td><td></td><td></td><td></td></tr><tr><th><b>VIII</b>. Southeast Africa</th><td>0.44 &ndash; 0.56 (0.51)</td><td>0.46 &ndash; 0.58 (0.51)</td><td>0.52 &ndash; 0.57 (0.54)</td><td>0.44 &ndash; 0.59 (0.51)</td><td>0.36 &ndash; 0.54 (0.46)</td><td>0.28 &ndash; 0.4 (0.35)</td><td>0.28 &ndash; 0.38 (0.34)</td><td><b>0</b>. <b>08</b></td><td></td><td></td></tr><tr><th><b>IX</b>. Southwestern</th><td>0.43 &ndash; 0.57 (0.51)</td><td>0.45 &ndash; 0.59 (0.52)</td><td>0.5 &ndash; 0.59 (0.55)</td><td>0.42 &ndash; 0.6 (0.52)</td><td>0.35 &ndash; 0.55 (0.47)</td><td>0.27 &ndash; 0.41 (0.34)</td><td>0.27 &ndash; 0.39 (0.34)</td><td>0 &ndash; 0.12 (0.05)</td><td></td><td><b>0</b>. <b>14</b></td></tr></tbody></table>

opencc-by-4.0Aug 2020View details →
zenodo28/100

Table 1 in Exogenous application of polyamines alleviates water stress-induced oxidative stress of Rosa damascena Miller var. trigintipetala Dieck

<p><b>Table 1</b> Effects of foliar application of spermine (Spm) and spermidine (Spd) on growth characters of <i>Rosa damascena</i> Miller var. <i>trigintipetala</i> Dieck plant grown under water stress (50% FC) or non-stress (100%FC) conditions.</p><table><tbody><tr><th>Treatments</th><th>Plant height (cm)</th><th>Plant FW (g)</th><th>Plant DW (g)</th></tr></tbody><tbody><tr><th>100% FC</th><td>Control</td><td>47.10 &plusmn; 0.85b</td><td>37.80 &plusmn; 0.72b</td><td>12.68 &plusmn; 0.45b</td></tr><tr><td>0.5 mM Spm</td><td>50.78 &plusmn; 0.38a</td><td>45.77 &plusmn; 1.66a</td><td>17.82 &plusmn; 0.64a</td></tr><tr><td>0.5 mM Spd</td><td>51.21 &plusmn; 1.07a</td><td>44.71 &plusmn; 0.50a</td><td>16.59 &plusmn; 0.52a</td></tr><tr><th>50% FC</th><td>Control</td><td>35.75 &plusmn; 0.66d</td><td>28.73 &plusmn; 0.64e</td><td>10.35 &plusmn; 0.59d</td></tr><tr><td>0.5 mM Spm</td><td>45.45 &plusmn; 0.78b</td><td>35.45 &plusmn; 1.72c</td><td>12.78 &plusmn; 0.27b</td></tr><tr><td>0.5 mM Spd</td><td>43.78 &plusmn; 0.70c</td><td>33.67 &plusmn; 2.08d</td><td>12.38 &plusmn; 0.15b</td></tr></tbody></table><p>Values are means &plusmn; S.D. (<i>n =</i> 8). Means within a column with different letters are significantly different from each other according to Duncan multiple range test at <i>P =</i> 0.05.</p>

opennotspecifiedMay 2018View details →
zenodo28/100

Table 2 in First insights into past biodiversity of giraffes based on mitochondrial sequences from museum specimens

<p><b>Table 2.</b> Museum specimens sequenced in this study (subspecies assignations have been made by morphological characters or distribution range). DRC = Democratic Republic of the Congo; SA = South Africa.</p><table><tbody><tr><th><b>Voucher</b></th><th><b>Subspecies</b></th><th><b>Collector, Date</b></th><th><b>Locality</b></th><th><b>N&deg; Accession</b></th></tr></tbody><tbody><tr><th><b>IRSNB-IG19076</b></th><td>?</td><td>Unknown, 1953</td><td>Anglo-Egyptian Sudan (Sudan / South Sudan)</td><td>MT542052</td></tr><tr><th><b>MNHN-A10753</b></th><td><i>peralta</i>?</td><td>G&eacute;rardin, 1830</td><td>Bakel, Senegal</td><td>MT542037</td></tr><tr><th><b>MNHN-A10617</b></th><td><i>peralta</i>?</td><td>G&eacute;rardin, 1830</td><td>Bakel, Senegal</td><td>MT542038</td></tr><tr><th><b>MNHN-1896-45</b></th><td><i>capensis</i></td><td>Delalande, 1818&ndash;1820</td><td>Cape of Good Hope (SA)</td><td>MT542039</td></tr><tr><th><b>MNHN-A10749</b></th><td><i>capensis</i></td><td>Delalande, 1818&ndash;1820</td><td>Cape of Good Hope (SA)</td><td>MT542040</td></tr><tr><th><b>MNHN-A7977</b></th><td><i>capensis</i></td><td>Levaillant, 1783&ndash;1785</td><td>Cape of Good Hope (SA)</td><td>MT542041</td></tr><tr><th><b>MNHN-1845-211</b></th><td><i>camelopardalis</i></td><td>Mouker Bey, 1824</td><td>Sennar (Sudan)</td><td>MT542042</td></tr><tr><th><b>MNHN-A8012</b></th><td><i>camelopardalis</i></td><td>Clot Bey, 1843</td><td>Abyssinia (Ethiopia)</td><td>MT542043</td></tr><tr><th><b>MNHN-1913-523</b></th><td><i>tippelskirchi</i>?</td><td>Babault, 1912&ndash;1913</td><td>Kenya</td><td>MT542054</td></tr><tr><th><b>MHNT-1996</b>. <b>121</b>. <b>2</b></th><td><i>camelopardalis</i></td><td>Unknown, 1843</td><td>Abyssinia (Ethiopia)</td><td>MT542044</td></tr><tr><th><b>RMCA-21645M</b></th><td><i>antiquorum</i></td><td>Huese, 1953</td><td>Sarh, Chad</td><td>MT542046</td></tr><tr><th><b>RMCA-25672M</b></th><td><i>congoensis</i></td><td>Poll, 1959</td><td>Gangala, DRC</td><td>MT542047</td></tr><tr><th><b>RMCA-25673M</b></th><td><i>congoensis</i></td><td>Poll, 1959</td><td>Gangala, DRC</td><td>MT542048</td></tr><tr><th><b>RMCA-83</b>. <b>006- M0553</b></th><td><i>congoensis</i></td><td>Colyn, 1946</td><td>Garamba Park, DRC</td><td>MT542049</td></tr><tr><th><b>RMCA-3748M</b></th><td><i>congoensis</i></td><td>De Calonne, 1914</td><td>Kapili, DRC</td><td>MT542050</td></tr><tr><th><b>RMCA-767M</b></th><td><i>cottoni</i></td><td>Powell-Cotton, 1908</td><td>Lado enclave, northwest Uganda and South Sudan</td><td>MT542051</td></tr><tr><th><b>RMCA-5956M</b></th><td><i>congoensis</i></td><td>Pilette, 1923</td><td>North-East Uele, DRC</td><td>MT542053</td></tr><tr><th><b>RMCA-2128M</b></th><td><i>tippelskirchi</i></td><td>Bayer, 1913</td><td>Serengeti-Mara, Kenya</td><td>MT542055</td></tr><tr><th><b>ZMB-48222</b></th><td>?</td><td>Unknown</td><td>Dikoa, Nigeria</td><td>MT542045</td></tr></tbody></table>

opencc-by-4.0Aug 2020View details →
zenodo28/100

TABLE 1 in Taxonomy and phylogeny of Hypoxylon zhaotongensis sp. nov. (Hypoxylaceae, Xylariales), a bambusicolous fungus from Yunnan, China

<p><b>TABLE 1.</b> Names, strain numbers, and corresponding GenBank accession numbers of the taxa used in this study. Cultures from holotype and epitype specimens are labeled as T and ET respectively. Species highlighted in bold were derived from this study. &ldquo;/&rdquo; means sequences data are unavailable in the GenBank database.</p><table><tbody><tr><th></th><th></th><th></th><th><b>GenBank accession numbers</b></th><th></th></tr></tbody><tbody><tr><th><b>Species name</b></th><td><b>Strain numbers</b></td><td><b>Types</b></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td><b>ITS</b></td><td><b>LSU</b></td><td><i>RPB2</i></td><td><i>&beta;-tubulin</i></td></tr><tr><th><i>Annulohypoxylon annulatum</i></th><td>CBS 140775</td><td>ET</td><td>KY610418</td><td>KY610418</td><td>KY624263</td><td>KX376353</td></tr><tr><th><i>Annulohypoxylon michelianum</i></th><td>CBS 119993</td><td></td><td>KX376320</td><td>KY610423</td><td>KY624234</td><td>KX271239</td></tr><tr><th><i>Annulohypoxylon truncatum</i></th><td>CBS 140778</td><td>ET</td><td>KY610419</td><td>KY610419</td><td>KY624277</td><td>KX376352</td></tr><tr><th><i>Daldinia bambusicola</i></th><td>CBS 122872</td><td>T</td><td>KY610385</td><td>KY610431</td><td>KY624241</td><td>AY951688</td></tr><tr><th><i>Daldinia childiae</i></th><td>CBS 122881</td><td>T</td><td>KU683757</td><td>MH874773</td><td>KU684290</td><td>KU684129</td></tr><tr><th><i>Daldinia concentrica</i></th><td>CBS 113277</td><td></td><td>AY616683</td><td>KY610434</td><td>KY624243</td><td>KC977274</td></tr><tr><th><i>Daldinia dennisii</i></th><td>CBS 114741</td><td>T</td><td>JX658477</td><td>KY610435</td><td>KY624244</td><td>KC977262</td></tr><tr><th><i>Daldinia eschscholtzii</i></th><td>MUCL 45435</td><td></td><td>JX658484</td><td>KY610437</td><td>KY624246</td><td>KC977266</td></tr><tr><th><i>Daldinia petriniae</i></th><td>MUCL 49214</td><td>ET</td><td>AM749937</td><td>KY610439</td><td>KY624248</td><td>KC977261</td></tr><tr><th><i>Daldinia placentiformis</i></th><td>MUCL 47603</td><td></td><td>AM749921</td><td>KY610440</td><td>KY624249</td><td>KC977278</td></tr><tr><th><i>Daldinia vernicosa</i></th><td>CBS 119316</td><td>ET</td><td>KY610395</td><td>KY610442</td><td>KY624252</td><td>KC977260</td></tr><tr><th><i>Durotheca rogersii</i></th><td>YMJ 92031201</td><td></td><td>EF026127</td><td>/</td><td>JX507794</td><td>EF025612</td></tr><tr><th><i>Durotheca comedens</i></th><td>YMJ 90071615</td><td>T</td><td>EF026128</td><td>/</td><td>JX507793</td><td>EF025613</td></tr><tr><th><b>Species name</b></th><td><b>Strain numbers</b></td><td><b>Types</b></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td><b>ITS</b></td><td><b>LSU</b></td><td><i>RPB2</i></td><td><i>&beta;-tubulin</i></td></tr><tr><th><i>Durotheca crateriformis</i></th><td>GMBC0205</td><td>T</td><td>MH645426</td><td>MH645425</td><td>MH645427</td><td>MH049441</td></tr><tr><th><i>Durotheca guizhouensis</i></th><td>GMBC0065</td><td>T</td><td>MH645423</td><td>MH645421</td><td>MH645422</td><td>MH049439</td></tr><tr><th><i>Durotheca rogersii</i></th><td>GMBC0204</td><td></td><td>MH645433</td><td>MH645434</td><td>MH645435</td><td>MH049449</td></tr><tr><th><i>Graphostroma platystomum</i></th><td>CBS 270.87</td><td>T</td><td>JX658535</td><td>DQ836906</td><td>KY624296</td><td>HG934108</td></tr><tr><th><i>Hypomontagnella barbarensis</i></th><td>STMA 14081</td><td>T</td><td>MK131720</td><td>MK131718</td><td>MK135891</td><td>MK135893</td></tr><tr><th><i>Hypomontagnella monticulosa</i></th><td>MUCL 54604</td><td></td><td>KY610404</td><td>KY610487</td><td>KY624305</td><td>KX271273</td></tr><tr><th><i>Hypomontagnella submonticulosa</i></th><td>CBS 115280</td><td></td><td>KC968923</td><td>KY610457</td><td>KY624226</td><td>KC977267</td></tr><tr><th><i>Hypoxylon addis</i></th><td>MUCL 52797</td><td>T</td><td>KC968931</td><td>ON954141</td><td>OP251037</td><td>KC977287</td></tr><tr><th><i>Hypoxylon aveirense</i></th><td>MUM 19.40</td><td>T</td><td>MN053021</td><td>ON954142</td><td>OP251028</td><td>MN066636</td></tr><tr><th><i>Hypoxylon baruense</i></th><td>UCH9545</td><td>T</td><td>MN056428</td><td>ON954143</td><td>/</td><td>MK908142</td></tr><tr><th><i>Hypoxylon canariense</i></th><td>MUCL 47224</td><td></td><td>ON792787</td><td>ON954140</td><td>OP251029</td><td>ON813073</td></tr><tr><th><i>Hypoxylon carneum</i></th><td>MUCL 54177</td><td></td><td>KY610400</td><td>KY610480</td><td>KY624297</td><td>KX271270</td></tr><tr><th><i>Hypoxylon cercidicola</i></th><td>CBS 119009</td><td></td><td>KC968908</td><td>KY610444</td><td>KY624254</td><td>KC977263</td></tr><tr><th><i>Hypoxylon chionostomum</i></th><td>STMA 14060</td><td></td><td>KU604563</td><td>ON954144</td><td>OP251030</td><td>ON813072</td></tr><tr><th><i>Hypoxylon chrysalidosporum</i></th><td>FCATAS2710</td><td>T</td><td>OL467294</td><td>OL615106</td><td>OL584222</td><td>OL584229</td></tr><tr><th><i>Hypoxylon crocopeplum</i></th><td>CBS 119004</td><td></td><td>KC968907</td><td>KY610445</td><td>KY624255</td><td>KC977268</td></tr><tr><th><i>Hypoxylon cyclobalanopsidis</i></th><td>FCATAS2714</td><td>T</td><td>OL467298</td><td>OL615108</td><td>OL584225</td><td>OL584232</td></tr><tr><th><i>Hypoxylon erythrostroma</i></th><td>MUCL 53759</td><td></td><td>KC968910</td><td>ON954154</td><td>OP251031</td><td>KC977296</td></tr><tr><th><i>Hypoxylon eurasiaticum</i></th><td>MUCL 57720</td><td>T</td><td>MW367851</td><td>/</td><td>MW373852</td><td>MW373861</td></tr><tr><th><i>Hypoxylon fendleri</i></th><td>MUCL 54792</td><td></td><td>KF234421</td><td>KY610481</td><td>KY624298</td><td>KF300547</td></tr><tr><th><i>Hypoxylon ferrugineum</i></th><td>CBS 141259</td><td></td><td>KX090079</td><td>/</td><td>/</td><td>KX090080</td></tr><tr><th><i>Hypoxylon fragiforme</i></th><td>MUCL 51264</td><td>ET</td><td>KC477229</td><td>KM186295</td><td>MK887342</td><td>KX271282</td></tr><tr><th><i>Hypoxylon fuscoides</i></th><td>MUCL 52670</td><td>T</td><td>ON792789</td><td>ON954145</td><td>OP251038</td><td>ON813076</td></tr><tr><th><i>Hypoxylon fuscum</i></th><td>CBS 113049</td><td>ET</td><td>KY610401</td><td>KY610482</td><td>KY624299</td><td>KX271271</td></tr><tr><th><i>Hypoxylon gibriacense</i></th><td>MUCL 52698</td><td>T</td><td>KC968930</td><td>ON954146</td><td>OP251026</td><td>ON813074</td></tr><tr><th><i>Hypoxylon griseobrunneum</i></th><td>CBS 331.73</td><td>T</td><td>KY610402</td><td>KY610483</td><td>KY624300</td><td>KC977303</td></tr><tr><th><i>Hypoxylon guilanense</i></th><td>MUCL 57726</td><td>T</td><td>MT214997</td><td>MT214992</td><td>MT212235</td><td>MT212239</td></tr><tr><th><i>Hypoxylon haematostroma</i></th><td>MUCL 53301</td><td>ET</td><td>KC968911</td><td>KY610484</td><td>KY624301</td><td>KC977291</td></tr><tr><th><i>Hypoxylon hainanense</i></th><td>FCATAS2712</td><td>T</td><td>OL467296</td><td>OL616132</td><td>OL584224</td><td>OL584231</td></tr><tr><th><i>Hypoxylon hinnuleum</i></th><td>ATCC 36255,MUCL 3621</td><td>T</td><td>MK287537</td><td>MK287549</td><td>MK287562</td><td>MK287575</td></tr><tr><th><i>Hypoxylon hongheensis</i></th><td>KUMCC 21-0452</td><td></td><td>OM001333</td><td>OM001334</td><td>ON392008</td><td>ON468655</td></tr><tr><th><i>Hypoxylon hongheensis</i></th><td>HKAS 122663</td><td>T</td><td>OM001336</td><td>OM001339</td><td>ON392009</td><td>ON468656</td></tr><tr><th><i>Hypoxylon howeanum</i></th><td>MUCL 47599</td><td></td><td>AM749928</td><td>KY610448</td><td>KY624258</td><td>KC977277</td></tr><tr><th><i>Hypoxylon hypomiltum</i></th><td>MUCL 51845</td><td></td><td>KY610403</td><td>KY610449</td><td>KY624302</td><td>KX271249</td></tr><tr><th><b>Species name</b></th><td><b>Strain numbers</b></td><td><b>Types</b></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td><b>ITS</b></td><td><b>LSU</b></td><td><i>RPB2</i></td><td><i>&beta;-tubulin</i></td></tr><tr><th><i>Hypoxylon invadens</i></th><td>MUCL 51475</td><td>T</td><td>MT809133</td><td>MT809132</td><td>MT813037</td><td>MT813038</td></tr><tr><th><i>Hypoxylon investiens</i></th><td>CBS 118183</td><td></td><td>KC968925</td><td>KY610450</td><td>KY624259</td><td>KC977270</td></tr><tr><th><i>Hypoxylon isabellinum</i></th><td>MUCL 53308</td><td>T</td><td>KC968935</td><td>/</td><td>OP251032</td><td>KC977295</td></tr><tr><th><i>Hypoxylon laschii</i></th><td>MUCL 52796</td><td></td><td>JX658525</td><td>/</td><td>OP251027</td><td>ON813075</td></tr><tr><th><i>Hypoxylon lateripigmentum</i></th><td>MUCL 53304</td><td>T</td><td>KC968933</td><td>KY610486</td><td>KY624304</td><td>KC977290</td></tr><tr><th><i>Hypoxylon lechatii</i></th><td>MUCL 54609</td><td></td><td>KF923407</td><td>/</td><td>OP251033</td><td>KF923405</td></tr><tr><th><i>Hypoxylon lenormandii</i></th><td>CBS 119003</td><td></td><td>KC968943</td><td>KY610452</td><td>KY624261</td><td>KC977273</td></tr><tr><th><i>Hypoxylon lienhwacheense</i></th><td>MFLUCC14-1231</td><td></td><td>KU604558</td><td>MK287550</td><td>MK287563</td><td>KU159522</td></tr><tr><th><i>Hypoxylon lividipigmentum</i></th><td>STMA14045</td><td></td><td>ON792788</td><td>/</td><td>/</td><td>ON813077</td></tr><tr><th><i>Hypoxylon lividipigmentum</i></th><td>BCRC 34077</td><td></td><td>JN979433</td><td>/</td><td>/</td><td>AY951735</td></tr><tr><th><i>Hypoxylon macrocarpum</i></th><td>CBS 119012</td><td></td><td>ON792785</td><td>/</td><td>OP251034</td><td>ON813071</td></tr><tr><th><i>Hypoxylon munkii</i></th><td>MUCL 53315</td><td></td><td>KC968912</td><td>/</td><td>OP251035</td><td>KC977294</td></tr><tr><th><i>Hypoxylon musceum</i></th><td>MUCL 53765</td><td></td><td>KC968926</td><td>KY610488</td><td>KY624306</td><td>KC977280</td></tr><tr><th><i>Hypoxylon ochraceum</i></th><td>MUCL 54625</td><td>ET</td><td>KC968937</td><td>/</td><td>KY624271</td><td>KC977300</td></tr><tr><th><i>Hypoxylon olivaceopigmentum</i></th><td>DSM 107924</td><td>T</td><td>MK287530</td><td>MK287542</td><td>MK287555</td><td>MK287568</td></tr><tr><th><i>Hypoxylon perforatum</i></th><td>CBS115281</td><td></td><td>KY610391</td><td>KY610455</td><td>KY624224</td><td>KX271250</td></tr><tr><th><i>Hypoxylon petriniae</i></th><td>CBS 114746</td><td>T</td><td>KY610405</td><td>KY610491</td><td>KY624279</td><td>KX271274</td></tr><tr><th><i>Hypoxylon pilgerianum</i></th><td>STMA 13455</td><td></td><td>KY610412</td><td>KY610412</td><td>KY624308</td><td>KY624315</td></tr><tr><th><i>Hypoxylon porphyreum</i></th><td>CBS 119022</td><td></td><td>KC968921</td><td>KY610456</td><td>KY624225</td><td>KC977264</td></tr><tr><th><i>Hypoxylon pseudofuscum</i></th><td>DSM112038</td><td>T</td><td>MW367857</td><td>MW367848</td><td>MW373858</td><td>MW373867</td></tr><tr><th><i>Hypoxylon pulicicidum</i></th><td>CBS 122622</td><td>T</td><td>JX183075</td><td>KY610492</td><td>KY624280</td><td>JX183072</td></tr><tr><th><i>Hypoxylon rickii</i></th><td>MUCL 53309</td><td>ET</td><td>KC968932</td><td>KY610416</td><td>KY624281</td><td>KC977288</td></tr><tr><th><i>Hypoxylon rubiginosum</i></th><td>MUCL 52887</td><td>ET</td><td>KC477232</td><td>KY610469</td><td>KY624266</td><td>KY624311</td></tr><tr><th><i>Hypoxylon samuelsii</i></th><td>MUCL 51843</td><td>ET</td><td>KC968916</td><td>KY610466</td><td>KY624269</td><td>KC977286</td></tr><tr><th><i>Hypoxylon sporistriatatunicum</i></th><td>UCH9542</td><td>T</td><td>MN056426</td><td>/</td><td>OP251036</td><td>MK908140</td></tr><tr><th><i>Hypoxylon subticinense</i></th><td>MUCL 53752</td><td></td><td>KC968913</td><td>/</td><td>/</td><td>KC977297</td></tr><tr><th><i>Hypoxylon texense</i></th><td>DSM 107933</td><td>T</td><td>MK287536</td><td>MK287548</td><td>MK287561</td><td>MK287574</td></tr><tr><th><i>Hypoxylon ticinense</i></th><td>CBS 115271</td><td></td><td>JQ009317</td><td>KY610471</td><td>KY624272</td><td>AY951757</td></tr><tr><th><i>Hypoxylon trugodes</i></th><td>MUCL 54794</td><td>ET</td><td>KF234422</td><td>KY610493</td><td>KY624282</td><td>KF300548</td></tr><tr><th><i>Hypoxylon vogesiacum</i></th><td>CBS 115273</td><td></td><td>KC968920</td><td>KY610417</td><td>KY624283</td><td>KX271275</td></tr><tr><th><i>Hypoxylon wuzhishanense</i></th><td>FCATAS2708</td><td>T</td><td>OL467292</td><td>OL615104</td><td>OL584220</td><td>OL584227</td></tr><tr><th><i>Hypoxylon zhaotongensis</i></th><td><b>GMBCC1168</b></td><td><b>T</b></td><td><b>OP597690</b></td><td><b>OP598100</b></td><td><b>OP615662</b></td><td><b>OP615660</b></td></tr><tr><th><i>Hypoxylon zhaotongensis</i></th><td><b>GMBCC1157</b></td><td></td><td><b>OP597691</b></td><td><b>OP598101</b></td><td><b>OP615663</b></td><td><b>OP615661</b></td></tr><tr><th><i>Jackrogersella cohaerens</i></th><td>CBS 119126</td><td></td><td>KY610396</td><td>KY610497</td><td>KY624270</td><td>KY624314</td></tr><tr><th><b>Species name</b></th><td><b>Strain numbers</b></td><td><b>Types</b></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td><b>ITS</b></td><td><b>LSU</b></td><td><i>RPB2</i></td><td><i>&beta;-tubulin</i></td></tr><tr><th><i>Jackrogersella multiformis</i></th><td>CBS 119016</td><td>ET</td><td>KC477234</td><td>KY610473</td><td>KY624290</td><td>KX271262</td></tr><tr><th><i>Natonodosa speciosa</i></th><td>CLM-RV86</td><td>T</td><td>MF380435</td><td>MF380435</td><td>MH745150</td><td>/</td></tr><tr><th><i>Parahypoxylon papillatum comb. nov.</i></th><td>ATCC 58729</td><td>T</td><td>KC968919</td><td>KY610454</td><td>KY624223</td><td>KC977258</td></tr><tr><th><i>Parahypoxylon ruwenzoriense sp. nov.</i></th><td>MUCL51392</td><td>T</td><td>ON792786</td><td>/</td><td>OP251039</td><td>ON813078</td></tr><tr><th><i>Pyrenopolyporus hunteri</i></th><td>MUCL 52673</td><td>ET</td><td>KY610421</td><td>KY610472</td><td>KY624309</td><td>KU159530</td></tr><tr><th><i>Pyrenopolyporus laminosus</i></th><td>MUCL 53305</td><td>T</td><td>KC968934</td><td>KY610485</td><td>KY624303</td><td>KC977292</td></tr><tr><th><i>Pyrenopolyporus nicaraguense</i></th><td>CBS 117739</td><td></td><td>AM749922</td><td>KY610489</td><td>KY624307</td><td>KC977272</td></tr><tr><th><i>Rhopalostroma angolense</i></th><td>CBS 126414</td><td></td><td>KY610420</td><td>KY610459</td><td>KY624228</td><td>KX271277</td></tr><tr><th><i>Rostrohypoxylon terebratum</i></th><td>CBS 119137</td><td>T</td><td>DQ631943</td><td>DQ840069</td><td>DQ631954</td><td>DQ840097</td></tr><tr><th><i>Ruwenzoria pseudoannulata</i></th><td>MUCL 51394</td><td>T</td><td>KY610406</td><td>KY610494</td><td>KY624286</td><td>KX271278</td></tr><tr><th><i>Thamnomyces dendroidea</i></th><td>CBS 123578</td><td>T</td><td>FN428831</td><td>KY610467</td><td>KY624232</td><td>KY624313</td></tr><tr><th><i>Xylaria arbuscula</i></th><td>CBS 126415</td><td></td><td>KY610394</td><td>KY610463</td><td>KY624287</td><td>KX271257</td></tr><tr><th><i>Xylaria hypoxylon</i></th><td>CBS 122620</td><td>ET</td><td>KY610407</td><td>KY610495</td><td>KY624231</td><td>KX271279</td></tr></tbody></table><p>......continued on the next page</p><p>......continued on the next page</p><p>......continued on the next page</p><p><b>Abbreviations: CBS:</b> Culture collection of the Westerdijk Fungal Biodiversity Institute, Utrecht, Netherlands; <b>MUCL:</b> Agrofood &amp; Environmental Fungal Collection; <b>GMBC:</b> Guizhou Medical University Culture Collection; <b>STMA:</b> HZI culture collection, Helmholtz Centre for Infection Research, Braunschweig, Germany; <b>MUM:</b> Micoteca da Universidade do Minho; <b>UCH:</b> Universidad Autonoma de Chiriqui; <b>FCATAS:</b> Fungarium of the Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences; <b>KUMCC:</b> Kunming Institute of Botany Culture Collection; <b>HKAS:</b> Cryptogamic Herbarium of Kunming Institute of Botany, Chinese Academy of Sciences; <b>MFLUCC:</b> Mae Fah Luang University Culture Collection, Chiang Rai, Thailand; <b>JF:</b> Jonkershoek Forestry Research Centre, Environment Affairs Department; <b>BCRC:</b> Bioresource Collection and Research Center; <b>DSM:</b> Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH; <b>GMBCC:</b> Guizhou Medical University Culture Collection, Guiyang, China; <b>CLM -RV:</b> -; <b>ATCC:</b> American Type Culture Collection; <b>YMJ:</b> YuMing, Ju; &ldquo;-&rdquo;: not available in the abbreviations.</p>

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Table 1 in Improvement of Pisum sativum salt stress tolerance by bio-priming their seeds using Typha angustifolia leaves aqueous extract

<p><b>Table 1</b> Germination percentage (%G) and germination index (GI) of not primed (NP) and primed (P) pea seeds, in presence of 0, 240, and 320 mM NaCl.</p><table><tbody><tr><th>NaCl (mM)</th><th>Seeds</th><th>% G</th><th>GI</th></tr></tbody><tbody><tr><th>0</th><td>NP</td><td>100a</td><td>5.22b</td></tr><tr><td>P</td><td>100a</td><td>6.72a</td></tr><tr><th>240</th><td>NP</td><td>51.25c</td><td>1.89d</td></tr><tr><td>P</td><td>66.25b</td><td>2.57c</td></tr><tr><th>320</th><td>NP</td><td>0e</td><td>0f</td></tr><tr><td>P</td><td>10d</td><td>0.33e</td></tr></tbody></table><p>Means with the same letters in a column are not significantly different at p &lt;0.05.</p>

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Table 2 in A new species of the genus Amerila Walker, 1855 from Tanzania (Lepidoptera: Erebidae: Arctiinae: Amerilini)

<p><b>Table 2</b>. Inter- and intraspecific K2P distances of COI-5P sequences in the <i>A. magnifica</i> species complex.</p><table><tbody><tr><th>COI-5P</th><th>A. magnifica ANLMN 3308 - 21</th><th>A. magnifica ANLMN 3309 - 21</th><th>A. mulleri CAM 101</th><th>A. mulleri CAM 158</th><th>A. mulleri CAM 102</th><th>A. mulleri CAM 159</th><th>A. francesae sp. n. NI 141</th><th>A. francesae sp. n. ANLMN 3427 -21</th></tr></tbody><tbody><tr><th><i>A. magnifica</i> ANLMN 3308-21</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>A. magnifica</i> ANLMN 3309-21</th><td>0,00%</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>A. mulleri</i> CAM 101</th><td>9,36%</td><td>9,36%</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>A. mulleri</i> CAM 158</th><td>9,36%</td><td>9,36%</td><td>0,00%</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>A. mulleri</i> CAM 102</th><td>9,18%</td><td>9,18%</td><td>0,15%</td><td>0,15%</td><td></td><td></td><td></td><td></td></tr><tr><th><i>A. mulleri</i> CAM 159</th><td>9,18%</td><td>9,18%</td><td>0,15%</td><td>0,15%</td><td>0,00%</td><td></td><td></td><td></td></tr><tr><th><i>A. francesae</i> <b>sp. n.</b> NI141</th><td>7,97%</td><td>7,97%</td><td>4,02%</td><td>4,02%</td><td>4,37%</td><td>4,37%</td><td></td><td></td></tr><tr><th><i>A. francesae</i> <b>sp. n.</b> ANLMN3427-21</th><td>8,33%</td><td>8,33%</td><td>6,09%</td><td>6,09%</td><td>6,26%</td><td>6,26%</td><td>0,65%</td><td></td></tr></tbody></table><p>0,65%</p>

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Table 2 in One in, one out: Generic circumscription within subtribe Manilkarinae (Sapotaceae)

<p><b>Table 2.</b> Characters and character states used for the morphological analyses and the ancestral state reconstructions (ASR).</p><table><tbody><tr><th>Characters</th><th>Abbreviations</th><th>Character states</th><th>Variable type (morphological analyses)</th><th>Character type (ASR)</th></tr></tbody><tbody><tr><th>Dorsal appendage dissection</th><td>App.Integr</td><td>Absent Entire Laciniate</td><td>Qualitative</td><td>Discrete</td></tr><tr><th>Staminode apex dissection</th><td>Stam.Integr</td><td>Absent Entire Toothed Laciniate</td><td></td><td></td></tr><tr><th>Ovary pubescence</th><td>Ov.Pub</td><td>Pubescent Glabrous</td><td></td><td></td></tr><tr><th>Merosity of corolla</th><td>Merosity</td><td>6 7 8 12 18</td><td>Quantitative integer</td><td></td></tr><tr><th>Number of ovary locules</th><td>Ov.locules</td><td>6 8 9 10 12</td><td></td><td></td></tr><tr><th>Total length of corolla (lobe + tube)</th><td>Cor.length</td><td>Millimeters</td><td>Quantitative continuous</td><td>Continuous</td></tr><tr><th>Corolla tube length to corolla lobe length ratio</th><td>Tube_Cor</td><td>Ratio</td><td></td><td></td></tr><tr><th>Dorsal appendage length to corolla lobe length ratio</th><td>App_Cor</td><td>Ratio</td><td></td><td></td></tr><tr><th>Staminode length to corolla lobe length ratio</th><td>Stam_Cor</td><td>Ratio</td><td></td><td></td></tr><tr><th>Style length to corolla lobe length ratio</th><td>Style_Cor</td><td>Ratio</td><td></td><td>Not used for ancestral state reconstruction</td></tr><tr><th>Staminode width to length ratio</th><td>Stam.l_L</td><td>Ratio</td><td></td></tr><tr><th>Corolla lobe width to length ratio</th><td>Cor.l_L</td><td>Ratio</td><td></td><td></td></tr><tr><th>Dorsal appendage width to length ratio</th><td>App.l_L</td><td>Ratio</td><td></td><td></td></tr></tbody></table>

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Table 1 in Taxonomy, phylogeny and biogeography of Politolana Bruce, 1981 (Crustacea: Isopoda: Cirolanidae)

<p><b>Table 1.</b> Measures of support for branches of <i>Politolana sensu stricto</i> (a monophyletic clade containing nine <i>Politolana</i> species, excluding the out-group genera and three outlying <i>Politolana</i> species: <i>P. dasyprion, P. obtusispina</i> and <i>P. crosnieri</i>)</p><table><tbody><tr><th>Branch #</th><th>Synapomorphies</th><th><i>b</i></th><th>Distance</th><th>Bootstrap</th></tr></tbody><tbody><tr><th>1</th><td>2</td><td>1</td><td>4</td><td>68%</td></tr><tr><th>2</th><td>3</td><td>3</td><td>5</td><td>86%</td></tr><tr><th>3</th><td>3</td><td>6</td><td>8</td><td>99%</td></tr><tr><th>4</th><td>2</td><td>3</td><td>4</td><td>78%</td></tr><tr><th>5</th><td>1</td><td>2</td><td>3</td><td>71%</td></tr><tr><th>6</th><td>2</td><td>2</td><td>3</td><td>66%</td></tr><tr><th>7</th><td>2</td><td>2</td><td>4</td><td>69%</td></tr><tr><th>8</th><td>0</td><td>1</td><td>1</td><td>52%</td></tr></tbody></table><p>Branch numbers correspond to Fig. 3. Synapomorphies include only those characters with a CI = 1; distance reflects the total amount of change on the branch, including homoplasious characters; <i>b</i> = Bremer support (decay index) of branch; bootstrap proportions are based on 1000 replicates, obtained with the heuristic search option in PAUP ver. 3.1.</p>

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TABLE 1 in Pterobryopsis siheiana (Bryophyta: Pterobryaceae) - a new species from the Western Ghats of India

<p><b>TABLE 1.</b> Specimen data and GenBank Accession numbers of the nuclear ITS sequences.</p><table><tbody><tr><th>Species</th><th>Isolate</th><th>Locality</th><th>Voucher</th><th>GenBank Accession #</th></tr></tbody><tbody><tr><th><i>Pterobryopsis schmidii</i></th><td>OK3793</td><td>India, Kerala, Idukki</td><td>Athira 319 p.p., SCCN</td><td>PP448000</td></tr><tr><th><i>Pterobryopsis divergens</i></th><td>OK3795</td><td>India, Kerala, Idukki</td><td>Athira 305 p.p., SCCN</td><td>PP448001</td></tr><tr><th><i>Pterobryopsis siheiana</i></th><td>OK3813</td><td>India, Kerala, Idukki</td><td>Athira 326 p.p., SCCN</td><td>PP448002</td></tr><tr><th><i>Pterobryopsis acuminata</i></th><td>OK3800</td><td>India, Kerala, Idukki</td><td>Athira 313 p.p., SCCN</td><td>PP448003</td></tr><tr><th><i>Pterobryopsis flexipes</i></th><td>OK3798</td><td>India, Tamil Nadu, Dindigul</td><td>Daniels 89, SCCN</td><td>PP448004</td></tr></tbody></table>

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Table 1 in Katydids (Orthoptera: Tettigoniidae) from Guartelá State Park, State of Paraná, Southern Brazil: diversity, bioacoustics and description of five new species

<p><b>Table 1.</b> Species of katydids collected in the Guartel&aacute; State Park, Brazil. Asterisks (*) indicate taxa that probably correspond to new species but are not described here.</p><table><tbody><tr><th>Taxa</th></tr></tbody><tbody><tr><th><b>CONOCEPHALINAE</b></th><td><b>PHANEROPTERINAE</b> (sequel)</td></tr><tr><th><b>Conocephalini</b></th><td><b>Odonturini</b> (sequel)</td></tr><tr><th><i>Conocephalus</i> (<i>Anisoptera</i>) <i>goianus</i></th><td><i>Xenicola nunoi</i> sp. nov.</td></tr><tr><th><i>Conocephalus</i> (<i>Anisoptera</i>) <i>guartela</i> sp. nov.</th><td><i>Xenicola xukrixi</i></td></tr><tr><th><i>Conocephalus</i> (<i>Anisoptera</i>) <i>saltator</i></th><td><b>Phaneropterini</b></td></tr><tr><th><i>Conocephalus</i> (<i>Anisoptera</i>) <i>truncatus</i></th><td><i>Anaulacomera angelinae</i></td></tr><tr><th><i>Conocephalus</i> (<i>Opeastylus</i>) <i>longipes</i></th><td><i>Anaulacomera trispinata</i></td></tr><tr><th>Conocephalini gen. et. sp. unknown</th><td><i>Anaulacomera</i> (<i>Anallomes</i>) <i>arlindoi</i></td></tr><tr><th><b>Copiphorini</b></th><td><i>Anaulacomera</i> (<i>Anallomes</i>) <i>sylviae</i></td></tr><tr><th><i>Lamniceps gigliotosi</i></th><td><i>Anaulacomera</i> (<i>Anaulacomera</i>) <i>longicercata</i></td></tr><tr><th><i>Neoconocephalus exaltatus</i></th><td><i>Anaulacomera</i> (<i>Anaulacomera</i>) <i>metropolitana</i></td></tr><tr><th><i>Neoconocephalus flavirostris</i></th><td><i>Anaulacomera</i> (<i>Anaulacomera</i>) <i>szinwelskii</i> sp. nov.</td></tr><tr><th><i>Neoconocephalus rioclarensis</i></th><td><i>Anaulacomera</i> (<i>Cervicercora</i>) <i>dama</i></td></tr><tr><th><i>Neoconocephalus spiniger</i></th><td><i>Anaulacomera</i> (<i>Cervicercora</i>) <i>melloi</i> sp. nov.</td></tr><tr><th><i>Neoconocephalus testaceus</i></th><td><i>Grammadera</i> (<i>Deragramma</i>) <i>albida</i></td></tr><tr><th><i>Neconocephalus vicinus</i></th><td><i>Grammadera</i> (<i>Deragramma</i>) <i>steinbachi</i></td></tr><tr><th><i>Neoconocephalus viridis</i></th><td><i>Grammadera</i> (<i>Grammadera</i>) <i>forcipata</i></td></tr><tr><th><i>Neoconocephalus</i> sp. 1 *</th><td><i>Phaneropteroides longicercatus</i></td></tr><tr><th><i>Neoconocephalus</i> sp. 2 *</th><td><i>Tomeophera modesta</i></td></tr><tr><th><i>Neoconocephalus</i> sp. 3 *</th><td><b>Phyllopterini</b></td></tr><tr><th><i>Neoconocephalus</i> sp. 4 *</th><td><i>Phylloptera fosteri</i></td></tr><tr><th><i>Oxyprora flavicornis</i></th><td><i>Phylloptera</i> sp. 1 *</td></tr><tr><th><b>MECONEMATINAE</b></th><td><b>Pycnopalpini</b></td></tr><tr><th><b>Phlugidini</b></th><td><i>Pycnopalpa bicordata</i></td></tr><tr><th><i>Phlugis</i> sp. 1 *</th><td><i>Topana</i> (<i>Topana</i>) <i>angulata</i></td></tr><tr><th><b>PHANEROPTERINAE</b></th><td><b>Scaphurae genus group</b></td></tr><tr><th><b>Aniarae genus group</b></th><td><i>Scaphura elegans</i></td></tr><tr><th><i>Aniarella minor</i></th><td><b>Scuderiini</b></td></tr><tr><th><i>Aniarella proxima</i></th><td><i>Ceraia cornutoides cornutoides</i></td></tr><tr><th><i>Hyperophora brasiliensis</i></th><td><i>Ceraia liebermanni</i></td></tr><tr><th><i>Hyperophora minor</i></th><td><i>Homotoicha similis</i></td></tr><tr><th><b>Cosmophylla genus group</b></th><td><i>Theudoria melanocnemis</i></td></tr><tr><th><i>Engonia minor</i></th><td><b>Steirodontini</b></td></tr><tr><th><i>Engonia</i> sp. 1 *</th><td><i>Stilpnochlora marginoides</i></td></tr><tr><th><b>Microcentrini</b></th><td><i>Incertae sedis</i></td></tr><tr><th><i>Microcentrum lanceolatum</i></th><td><i>Enthephippion olivaceum</i></td></tr><tr><th><b>Odonturini</b></th><td><b>PSEUDOPHYLLINAE</b></td></tr><tr><th><i>Anisophya melanochloris</i></th><td><b>Cocconotini</b></td></tr><tr><th><i>Anisophya hemanuelae</i> sp. nov.</th><td>Dasyscelus intermedius</td></tr></tbody></table>

opennotspecifiedJul 2023View details →
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TABLE 8 in Horses in the suburbs of a medieval city - a case study from Brno (Czech Republic)

<p>TABLE 8. &mdash; Recorded scores for the ossification of interosseous ligaments between metapodials of the horses from Brno.</p><table><tbody><tr><th></th><th></th><th><b>Left</b></th><th><b>Right</b></th><th><b>Left</b></th><th><b>Right</b></th><th></th></tr></tbody><tbody><tr><th></th><td></td><td><b>metacarpal metacarpal metatarsal metatarsal</b></td></tr><tr><th></th><td><b>Age</b></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>ID</b></th><td><b>(years)</b></td><td><b>II-III</b></td><td><b>III-IV</b></td><td><b>II-III</b></td><td><b>III-IV</b></td><td><b>II-III</b></td><td><b>III-IV</b></td><td><b>II-III</b></td><td><b>III-IV</b></td></tr><tr><th>T_1490</th><td>10-13</td><td>0</td><td>0</td><td>0</td><td>0</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td></tr><tr><th>T_3256</th><td>10-11</td><td>2</td><td>1b</td><td>1b</td><td>1b</td><td>0</td><td>0</td><td>0</td><td>0</td></tr><tr><th>T_3257</th><td>7-8</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td></tr><tr><th>T_3258</th><td>9-11</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>T_3164</th><td>&gt;5</td><td>2</td><td>0</td><td>2</td><td>0</td><td>2</td><td>0</td><td>2</td><td>0</td></tr><tr><th>M_802</th><td>12-14</td><td>2</td><td>1b</td><td>2</td><td>2</td><td>0</td><td>2</td><td>0</td><td>1b</td></tr><tr><th>K_800</th><td>&lt;3-3.5</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td><td>&ndash;</td></tr><tr><th>K_801</th><td>3-4</td><td>1c</td><td>1c</td><td>1c</td><td>0</td><td>0</td><td>0</td><td>0</td><td>0</td></tr><tr><th>K_802</th><td>9-11</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></tbody></table>

opencc-by-4.0Nov 2024View details →
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TABLE 3 in Horses in the suburbs of a medieval city - a case study from Brno (Czech Republic)

<p>TABLE 3. &mdash; Mod&rcaron;ice: list of horse burials</p><table><tbody><tr><th><b>Skeleton Number Preservation</b></th><th><b>Pit description Dating Figure</b></th></tr></tbody><tbody><tr><th>M_802</th><td>Postcranial skeleton and seven loose teeth (3 x I1-3, 1 x C, 2 x upper P2,</td><td>Oval.</td><td>15th-16th century.</td><td>12</td></tr><tr><th></th><td>1 x upper P3). Four horse shoes <i>in situ</i>.</td><td></td><td></td><td></td></tr><tr><th>M_803</th><td>Complete skeleton of a newborn foal.</td><td>Oval.</td><td>15th-16th century.</td><td>12</td></tr></tbody></table>

opencc-by-4.0Nov 2024View details →
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The supporting information for the Gega Megaflood and Yigong Superflood contains additional information, including methods, tables, figures.

Open the record for dataset details and reuse information.

opencc-by-4.0Oct 2024View details →
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Additional information and tables for: Association of circulating metabolites in plasma or serum and risk of stroke: Meta-analysis from seven prospective cohorts

<p><b>Objective: </b>To conduct a comprehensive analysis of circulating metabolites and incident stroke in large prospective population-based settings.</p> <p><b>Methods: </b>We investigated the association of metabolites with risk of stroke in seven prospective cohort studies including 1,791 incident stroke events among 38,797 participants in whom circulating metabolites were measured by Nuclear Magnetic Resonance (<sup>1</sup>H-NMR) technology. The relationship between metabolites and stroke was assessed using Cox proportional hazards regression models. The analyses were performed considering all incident stroke events and ischemic and hemorrhagic events separately.</p> <p><b>Results: </b>The analyses revealed ten significant metabolite associations. Amino acid histidine (hazard ratio (HR) per standard deviation (SD) = 0.90, 95% confidence interval (CI): 0.85, 0.94; <i>P</i> = 4.45×10<sup>-5</sup>), glycolysis-related metabolite pyruvate (HR per SD = 1.09, 95% CI: 1.04, 1.14; <i>P</i> = 7.45×10<sup>-4</sup>), acute phase reaction marker glycoprotein acetyls (HR per SD = 1.09, 95% CI: 1.03, 1.15; <i>P</i> = 1.27×10<sup>-3</sup>), cholesterol in high-density lipoprotein (HDL) 2 and several other lipoprotein particles were associated with risk of stroke. When focusing on incident ischemic stroke, a significant association was observed with phenylalanine (HR per SD = 1.12, 95% CI: 1.05, 1.19; <i>P = </i>4.13×10<sup>-4</sup>) and total and free cholesterol in large HDL particles.</p> <p><b>Conclusions: </b>We found association of amino acids, glycolysis-related metabolites, acute phase reaction markers, and several lipoprotein subfractions with the risk of stroke. These findings support the potential of metabolomics to provide new insights into the metabolic changes preceding stroke.</p>

opencc-zeroDec 2021View details →
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Table S1

<p>This table is the experiment results for topaz up to 13 GPa at room temperature</p>

opencc-by-4.0Jul 2021View details →
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Table S1 for Yeager, et al. Biomolecules 2021

<p>Differentially abundant transcripts in spores sorted by mating type, according to edgeR analysis.</p>

opencc-by-4.0Jul 2021View details →
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Table e-1 and e-references for: Neurogenic dysphagia: a systematic review and proposal of a classification system

<p><b>Objective:</b> Introduction of a phenotypic classification of dysphagia with differential diagnostic implications and its validation in different disease groups using videos of flexible endoscopic evaluation of swallowing (FEES).</p> <p><b>Methods: </b>A systematic literature review was performed to summarize disease-typical FEES-findings.<b> </b>In an interdisciplinary team, a FEES-based classification of neurogenic dysphagia was developed which distinguishes different dysphagia phenotypes. The classification was validated using 1012 randomly selected FEES videos of patients with various neurological disorders. Chi-square tests were applied to investigate the relationship between the disease groups and each dysphagia phenotype.</p> <p><b>Results: </b>Seven dysphagia phenotypes were defined and all phenotypes were significantly  associated with specific neurological disease groups: (1) "Premature bolus spillage" and (2) "delayed swallowing reflex" occurred mainly in stroke patients, (3) "predominance of residue in the valleculae" was most common in Parkinson's disease, (4) "predominance of residue in the piriform sinus" occurred only in myositis, motoneuron disease and brainstem stroke patients, (5) "pharyngolaryngeal movement disorder" was found in atypical Parkinsonian syndromes and stroke patients, (6) "fatigable swallowing weakness" was common in patients with myasthenia gravis, and (7) "complex disorder" with a heterogeneous dysphagia pattern was the leading mechanism in amyotrophic later sclerosis. The interrater reliability showed a strong agreement (kappa = 0.84).</p> <p><b>Conclusion: </b>Neurogenic dysphagia is not a mere symptom, but a multi-etiological syndrome with different phenotypic patterns depending on the underlying disease. Dysphagia phenotypes can facilitate differential diagnosis in patients with dysphagia of unclear etiology.</p>

opencc-zeroOct 2021View details →
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FIGURE 11 in Table 7

FIGURE 11. Habitat of Ancyronyx yunju sp. nov. [photo by Tong]

opennotspecifiedApr 2012View details →
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bed12 tables for hg19, dm6 and ce11

<p>tables for tandem exon duplication analysis</p>

opencc-by-4.0Sep 2021View details →

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