Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
19,468
datasets available to search
ShareScore release 0.9.0
Dataset results
19,468 results for “p”
Physical and Tsfel Features for (P_10_30_F_05_15_50)
<p>Physical and Tsfel Features for four classes of events that dominate the seismicity in the pacific northwest. Before extracting the features, following processing was applied - </p> <ul> <li>trimming (first arrival - 10, first arrival +30)</li> <li>detrending</li> <li>resampling to 100 Hz</li> <li>cosine taper (10%)</li> <li>bandpass filtered (0.5 - 15 Hz)</li> <li>normalizing by maximum</li> <li>resampling to 50 Hz</li> </ul>
Mapa 1.- 1a. P in Nuevos registros de pirocroidos (Coleoptera, Pyrochroidae) para Galicia (N.O. Península Ibérica).
Mapa 1.- 1a. P. coccinea (L.) 1b. P. serraticornis (Scop.) z citas bibliográficas z citas nuevas
Data for: Synergistic mechanisms of plant phosphorus (P) resorption and microbial P-limitation affecting soil P during grassland vegetation succession
<p>Data for: <strong>Synergistic mechanisms of plant phosphorus (P) resorption and microbial P-limitation affecting soil P during grassland vegetation succession</strong></p>
Whole-mantle P-wave isotropic and anisotropic tomography beneath Japan and adjacent regions
<p>Dear readers,</p> <p>A file named "Japan_ISO.dat" contains whole-mantle P-wave isotropic tompgraphy beneath Japan and surrounding regions.</p> <p>The data format is as follows:<br>1st column: depth (km) (F8.2)<br>2nd column: latitude (deg) (F8.2)<br>3rd column: longitude (deg) (F8.2)<br>4th column: dVp (%) (F8.2)<br>5th column: Ray hit count (I8)</p> <p>These are values on grid points used for tomographic inversion.</p> <p>A file named "Japan_AAN_iso.dat" contains isotropic component of whole-mantle P-wave azimuthal anisotropy (AAN) tompgraphy beneath Japan and surrounding regions. </p> <p>The data format is as follows:<br>1st column: depth (km) (F8.2)<br>2nd column: latitude (deg) (F8.2)<br>3rd column: longitude (deg) (F8.2)<br>4th column: dVp (%) (F8.2)<br>5th column: Ray hit count (I8)</p> <p>These are values on grid points used for tomographic inversion.</p> <p>A file named "Japan_AAN_ai.dat" contains anisotropic component of whole-mantle P-wave azimuthal anisotropy (AAN) tompgraphy beneath Japan and surrounding regions. </p> <p>The data format is as follows:<br>1st column: depth (km) (F10.3)<br>2nd column: latitude (deg) (F10.3)<br>3rd column: longitude (deg) (F10.3)<br>4th column: Anisotropic amplitude (%) (F10.3)<br>5th column: Fast velocity direction (deg) (F10.3)</p> <p>These values are obtained by interpolation from the values at surrounding anisotropic grid points used for tomographic inversion.</p> <p>We hope it is useful to you.</p> <p>Kind wishes,</p> <p>Genti Toyokuni & Dapeng Zhao<br>Tohoku University, Japan<br>E-mail: toyokuni@tohoku.ac.jp</p> <p>Reference:<br>Toyokuni, G., Zhao, D., & Takada, D. (2024).<br>Whole-mantle isotropic and anisotropic tomography beneath Japan and adjacent regions.<br>Journal of Geophysical Research: Solid Earth, under review.</p>
Table 2 in Effects of different combinations of N, P and K at different time interval on vegetative, reproductive, yield and quality traits of mango (Mangifera Indica. L) cv. Dusehri
<p><b>Table 2.</b> Effect of different fertilizer combinations of N, P and K on reproductive physiology of mango cv. Dusehri.</p><table><tbody><tr><th><b>Treatments</b></th><th><b>Growth size (mm)</b></th><th><b>Total No. of Panicle/Tree</b></th><th><b>Total no. of flowers / Panicle</b></th><th><b>Sex Ratio (%)</b></th><th><b>Fruit Drop (%)</b></th><th><b>Fruit Retention (%)</b></th><th><b>Total no. of fruit/tree</b></th><th><b>Yield (Kg/Tree)</b></th><th><b>Fruit Length (cm)</b></th><th><b>Fruit Weight (g)</b></th><th><b>Pulp Weight (g)</b></th><th><b>Stone Weight (g)</b></th><th><b>Peel Weight (g)</b></th><th><b>TSS (%)</b></th><th><b>Total Acidity (%)</b></th><th><b>TSS/Acid Ratio</b></th><th><b>Vit. C (mg/100 mL)</b></th><th><b>Total Sugar (%)</b></th></tr></tbody><tbody><tr><th>T1 (Control)</th><td>149.34d ± 3.89</td><td>397.67h ± 3.51</td><td>543.21h ± 3.61</td><td>51.17c ± 2.10</td><td>94.85a ± 1.40</td><td>1.83e ± 0.15</td><td>186.72g ± 4.51</td><td>40.01e ± 4.51</td><td>15.4b ± 3.17</td><td>155.15e ± 6.34</td><td>76.30g ± 2.22</td><td>24.14f ± 2.02</td><td>28.61f ± 1.86</td><td>20.29d ± 1.05</td><td>0.52a ± 0.005</td><td>22.43</td><td>31.26f ± 0.92</td><td>14.52c ± 0.25</td></tr><tr><th>T2 (N)</th><td>166.67b ± 4.47</td><td>508.57f ± 4.51</td><td>612.47f ± 4.58</td><td>54.42bc ± 1.05</td><td>94.86a ± 2.41</td><td>5.57d ± 0.57</td><td>213.34f ± 3.06</td><td>52.70cd ± 4.50</td><td>16.4b ± 3.11</td><td>175.50bc ± 5.50</td><td>82.41f ±1.90</td><td>30.04de ± 2.21</td><td>33.70e ± 1.38</td><td>21.06cd ± 0.95</td><td>0.49b ± 0.004</td><td>25.16</td><td>42.22c ± 1.18</td><td>15.24bc ± 0.41</td></tr><tr><th>T3 (P)</th><td>156.26cd ± 4.85</td><td>467.33g ± 4.04</td><td>593.34g ± 3.61</td><td>53.57bc ± 1.01</td><td>91.72ab± 2.51</td><td>8.82bc ± 0.72</td><td>241.40e ± 4.04</td><td>50.14d ± 5.03</td><td>18.3ab ± 2.75</td><td>169.24cd ± 5.41</td><td>85.23f ± 1.96</td><td>28.50e ± 2.00</td><td>35.62de ±1.94</td><td>22.07bc ± 1.10</td><td>0.45c ± 0.005</td><td>29.13</td><td>39.37d ± 0.98</td><td>15.82bc ± 0.29</td></tr><tr><th>T4 (K)</th><td>164.80bc ± 4.95</td><td>634.57c ± 4.51</td><td>730.19c ± 4.56</td><td>57.39bc ± 2.38</td><td>94.26ab ± 1.79</td><td>5.83d ± 0.48</td><td>278.33d ± 3.51</td><td>55.23cd ± 4.50</td><td>19.3ab ± 2.99</td><td>182.01b ± 5.47</td><td>99.92e ± 1.89</td><td>31.26e ± 1.76</td><td>40.84c ± 1.35</td><td>21.41cd ± 1.25</td><td>0.37d ± 0.002</td><td>43.27</td><td>36.62e ± 1.21</td><td>16.89b ± 0.55</td></tr><tr><th>T5 (NP)</th><td>166.48b ± 4.98</td><td>584.47d ± 3.51</td><td>639e.46 ± 4.04</td><td>56.61bc ± 1.59</td><td>93.34ab ± 2.15</td><td>6.92cd ± 0.33</td><td>288.62c ± 4.51</td><td>57.31c ± 5.03</td><td>17.2b ± 3.29</td><td>160.46de ±4.86</td><td>107.34c ± 2.11</td><td>35.63bc ± 2.02</td><td>37.81d ± 1.88</td><td>23.43ab ± 0.93</td><td>0.35d ± 0.001</td><td>40.48</td><td>42.09b ± 0.47</td><td>16.65b ± 0.61</td></tr><tr><th>T6 (NK)</th><td>160.75bc ± 5.05</td><td>684.66b ± 4.50</td><td>810.62b ± 4.59</td><td>60.17b ± 2.53</td><td>90.28cd ± 2.71</td><td>9.74ab ± 0.66</td><td>320.32b ± 3.05</td><td>66.61b ± 4.49</td><td>18.5ab ± 2.73</td><td>180.32b ± 5.35</td><td>118.04b ± 1.94</td><td>37.21b ± 1.81</td><td>46.92b ± 1.65</td><td>23.30ab ± 0.08</td><td>0.32e ± 0.002</td><td>51.28</td><td>51.48b ±1.07</td><td>16.07b ± 0.71</td></tr><tr><th>T7 (PK)</th><td>159.42bc ± 4.98</td><td>559.71e ± 3.49</td><td>701.17d ± 3.61</td><td>55.31bc ± 1.02</td><td>92.96ab ± 2.56</td><td>7.49bcd ± 0.52</td><td>274.37d ± 2.52</td><td>54.85cd ± 4.51</td><td>18.1b ± 3.01</td><td>178.24bc ± 6.53</td><td>103.51d ± 1.79</td><td>33.07cd ± 1.95</td><td>42.14c ± 1.43</td><td>2.35bc ± 0.05</td><td>0.31e ± 0.002</td><td>52.41</td><td>51.55b ± 0.95</td><td>15.01b ± 0.37</td></tr><tr><th>T8 (NPK)</th><td>177.51a ± 4.92</td><td>845.64a ± 3.61</td><td>974.52a ± 4.58</td><td>69.18a ± 2.87</td><td>86.10e ± 2.85</td><td>13.85a ± 0.43</td><td>379.05a ± 3.00</td><td>82.35a ± 3.51</td><td>23.3a ± 3.10</td><td>197.05a ± 5.62</td><td>135.32a ± 2.09</td><td>43.53a ± 2.07</td><td>52.09a ± 1.77</td><td>24.53a ± 0.06</td><td>0.26f ± 0.001</td><td>73.53</td><td>57.63a ± 0.07</td><td>20.48a ± 0.53</td></tr></tbody></table><p>Values within each column followed by the same letter are not significantly different at P <0.5 level.</p><p>Values within each column followed by the same letter are not significantly different at <i>P</i> <0.05 level.</p><p>Values within each column followed by the same letters are not significantly different at <i>P</i> <0.05 level.</p>
Table 1 K 2 P in Sand fly fauna of South-Eastern Romania, with the description of PhlebotomUS (TranSphlebotomUS) Simonahalepae n. sp. (Diptera: Psychodidae)
<p><b>Table 1</b> K2P sequence divergence (<i>Cytb</i> / <i>CO1</i> / <i>ND4</i>) between the species belonging to the subgenus Transphlebotomus</p><table><tbody><tr><th></th><th><i>Ph</i>. <i>anatolicus</i></th><th><i>Ph</i>. <i>canaaniticus</i></th><th><i>Ph.economidesi</i></th><th><i>Ph</i>. <i>killicki</i></th><th><i>Ph</i>. <i>mascittii</i></th><th><i>Ph</i>. <i>simonahalepae</i> n. sp.</th></tr><tr><th><i>Ph</i>. <i>anatolicus</i></th></tr></tbody><tbody><tr><th><i>Ph</i>. <i>canaaniticus</i></th><td>0.069/0.068/na</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Ph.economidesi</i></th><td>0.107/0.146/na</td><td>0.112/0.131/0.103</td><td></td><td></td><td></td><td></td></tr><tr><th><i>Ph</i>. <i>killicki</i></th><td>0.107/0.146/na</td><td>0.103/0.111/0.097</td><td>0.083/0.131/0.096</td><td></td><td></td><td></td></tr><tr><th><i>Ph</i>. <i>mascittii</i></th><td>0.107/0.146/na</td><td>0.120/0.104/0.116</td><td>0.116/0.150/0.105</td><td>0.106/0.115/0.117</td><td></td><td></td></tr><tr><th><i>Ph</i>. <i>simonahalepae</i> n. sp.</th><td>0.107/0.146/na</td><td>0.122/0.112/0.116</td><td>0.075/0.090/0.075</td><td>0.086/0.110/0.101</td><td>0.121/0.115/0.112</td><td></td></tr></tbody></table><p><i>na</i> not available</p>
Whole-mantle P-wave isotropic tomography beneath Australia and New Zealand
<p>Dear readers,</p> <p>A file named "AN_ISO.dat" contains whole-mantle P-wave isotropic tompgraphy beneath Australia and New Zealand.</p> <p>The data format is as follows:<br>1st column: depth (km) (F7.2)<br>2nd column: latitude (deg) (F7.2)<br>3rd column: longitude (deg) (F7.2)<br>4th column: dVp (%) (F7.2)<br>5th column: Ray hit count (I8)</p> <p>These are values on grid points used for tomographic inversion.</p> <p>We hope it is useful to you.</p> <p>Kind wishes,</p> <p>Genti Toyokuni & Dapeng Zhao<br>Tohoku University, Japan<br>E-mail: toyokuni@tohoku.ac.jp</p> <p>Reference:<br>Toyokuni, G. & Zhao, D. (2024).<br>Slab-plume interactions beneath Australia and New Zealand: New insight from whole-mantle tomography.<br>Geochemistry, Geophysics, Geosystems, under review.</p>
Table 3. Uncorrected p in A New Species of Murina (Chiroptera: Vespertilionidae) from Yunnan, China
<p><b>Table 3.</b> Uncorrected <i>p</i> -distances (%) between species calculated from 657 bp COI gene fragment. Values less than or equal to <i>p</i> -distances between our specimen and <i>M. chrysochaetes</i> are underlined.</p><table><thead><tr><th>No.</th><th>Taxon</th><th>1</th><th>2</th><th>3</th><th>4</th><th>5</th><th>6</th><th>7</th><th>8</th><th>9</th><th>10</th><th>11</th><th>12</th><th>13</th><th>14</th></tr></thead><tbody><tr><th>1</th><td><i>M. yuanyang</i> sp. Nov. (KIZ20230415)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>2</th><td><i>M. yuanyang</i> sp. Nov. (KIZ20230424)</td><td>0.0</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>3</th><td><i>M. yuanyang</i> sp. Nov. (KIZ20230426)</td><td>0.0</td><td>0.0</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>4</th><td><i>M. yuanyang</i> sp. Nov. (KIZ20230449)</td><td>0.0</td><td>0.0</td><td>0.0</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>5</th><td><i>M. yuanyang</i> sp. Nov. (KIZ20230492)</td><td>0.0</td><td>0.0</td><td>0.0</td><td>0.0</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>6</th><td><i>M. yuanyang</i> sp. Nov. (KIZ20230498)</td><td>0.3</td><td>0.3</td><td>0.3</td><td>0.3</td><td>0.3</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>7</th><td><i>M. chrysochaetes</i></td><td>2.7</td><td>2.7</td><td>2.7</td><td>2.7</td><td>2.7</td><td>3.0</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>8</th><td><i>M. harpioloides</i></td><td>9.0</td><td>9.0</td><td>9.0</td><td>9.0</td><td>9.0</td><td>9.3</td><td>9.4</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>9</th><td><i>M. eleryi</i></td><td>16.3</td><td>16.3</td><td>16.3</td><td>16.3</td><td>16.3</td><td>16.3</td><td>17.2</td><td>16.5</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>10</th><td><i>M. leucogaster</i></td><td>17.0</td><td>17.0</td><td>17.0</td><td>17.0</td><td>17.0</td><td>17.4</td><td>16.9</td><td>16.0</td><td>16.6</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>11</th><td><i>M. rongjiangensis</i></td><td>16.6</td><td>16.6</td><td>16.6</td><td>16.6</td><td>16.6</td><td>16.9</td><td>17.0</td><td>16.0</td><td>15.7</td><td>4.3</td><td></td><td></td><td></td><td></td></tr><tr><th>12</th><td><i>M. shuipuensis</i></td><td>17.5</td><td>17.5</td><td>17.5</td><td>17.5</td><td>17.5</td><td>17.8</td><td>17.7</td><td>16.4</td><td>16.1</td><td>2.6</td><td>4.1</td><td></td><td></td><td></td></tr><tr><th>13</th><td><i>M. gracilis</i></td><td>17.8</td><td>17.8</td><td>17.8</td><td>17.8</td><td>17.8</td><td>17.8</td><td>18.8</td><td>17.5</td><td>9.6</td><td>17.5</td><td>16.6</td><td>17.0</td><td></td><td></td></tr><tr><th>14</th><td><i>M. recondita</i></td><td>19.1</td><td>19.1</td><td>19.1</td><td>19.1</td><td>19.1</td><td>19.1</td><td>20.0</td><td>18.6</td><td>10.7</td><td>18.4</td><td>17.2</td><td>17.5</td><td>4.2</td><td></td></tr></tbody></table>
Dataset for the publication: Synthesis, Characterization and Interconversion of p-Tolylsulfone-Functionalized Norbornadiene/Quadricyclane Couples
<p>Overview of all collected data used for the publication "Synthesis, Characterization and Interconversion of p-Tolylsulfone-Functionalized Norbornadiene/Quadricyclane Couples" in the journal Chemistry - A European Journal.</p>
TABLEAU 2 in Identité d'Amphorkis inermis Thouars et d'Arnottia mauritiana A. Rich.: deux espèces distinctes, traitées en synonymie comme Cynorkis inermis (Thouars) Hermans & P. J. Cribb dans la Flore des Mascareignes
<p>TABLEAU 2. — Caractères distinctifs de <i>Cynorkis inermis</i> (P00738182; MAU0012611; MAU001534; MAU001535) et <i>Cynorkis mauritiana</i> comb.nov. (P00738198; P00738214; P00738203; P00738209) mesurés en mm à partir d’exsicatas (réhydratés pour les pièces florales). Les valeurs indiquées sont: <b>min-max</b>, moyenne; <b>L</b>, longueur; <b>l</b>, largeur.</p><table><tbody><tr><th></th><th><i>Cynorkis inermis</i></th><th><i>Cynorkis mauritiana</i> <b>comb. nov.</b></th></tr><tr><th></th><th><b>N = 4</b></th></tr><tr><th></th><th><b>N = 4</b></th></tr></tbody><tbody><tr><th>Feuille (L)</th><td>101 (77-121)</td><td>122 (82-202)</td></tr><tr><th>Feuille (l)</th><td>12 (11-15)</td><td>25 (16-38)</td></tr><tr><th>Tige (L)</th><td>170 (131-221)</td><td>161 (131-197)</td></tr><tr><th>Bractée stérile (L)</th><td>8,8 (7,8-10,2)</td><td>16,7 (10,8-23,2)</td></tr><tr><th>Bractée fertile (L)</th><td>5,1 (4,1-6,0)</td><td>5,2 (5-5,6)</td></tr><tr><th>Ovaire (L)</th><td>5,6 (5,0-6,5)</td><td>13,7 (12-15)</td></tr><tr><th>Sépale dorsal (L)</th><td>4,1 (3,8-4,5)</td><td>6,1 (5,7-6,5)</td></tr><tr><th>Sépale dorsal (l)</th><td>1,9 (1,8-2,0)</td><td>3,0 (2,6-3,3)</td></tr><tr><th>Sépale latéral (L)</th><td>4,6 (4,1- 5,3)</td><td>9,0 (7,2-10,8)</td></tr><tr><th>Sépale latéral (l)</th><td>2,2 (2,3-2,2)</td><td>4,2 (3,3-5,4)</td></tr><tr><th>Pétale (L)</th><td>4,0 (3,6-4,5)</td><td>6,1(5,5-6,8)</td></tr><tr><th>Pétal (l)</th><td>1,1 (1,0-1,2)</td><td>2,1 (1,5-2,5)</td></tr><tr><th>Labelle (L)</th><td>4,0 (3,5- 4,6)</td><td>6,8 (5,9-7,5)</td></tr><tr><th>Labelle (l)</th><td>1,1 (1,0-1,3)</td><td>2,6 (2,2-3,0)</td></tr></tbody></table>
p-IgGen Dataset: Cleaned paired and unpaired antibody sequence data for machine learning applications.
<p>This data is released alongside "p-IgGen: A Paired Antibody Generative Language Model", which contains full details on the data processing and cleaning.</p> <p>p-IgGen Paper: https://www.biorxiv.org/content/10.1101/2024.08.06.606780v1 .</p> <p>OAS: https://opig.stats.ox.ac.uk/webapps/oas/</p> <p> </p>
TABLE 3 in Taxonomic status of the Western Hemispingus Sphenopsis ochracea (Thraupidae) and a review of species limits in the genus Sphenopsis P. L. Sclater, 1861
<p>TABLE 3</p><table><thead><tr><th>Sex</th><th><b>Species</b></th><th><i>n</i></th><th>WG</th><th>TR</th><th>TL</th><th>BL</th><th><b>BW</b></th></tr></thead><tbody><tr><th>female</th><td><i>S. melanotis melanotis</i></td><td>5</td><td>73.2 ± 1.6</td><td>19.9 ± 0.3</td><td>62.8 ± 2.4</td><td>8.2 ± 0.3</td><td>3.9 ± 0.1</td></tr><tr><th></th><td><i>S. m. castaneicollis</i></td><td>3</td><td>61.7 ± 1.5</td><td>21.3 ± 2.1</td><td>55.0 ± 2.8</td><td>7.6 ± 0.4</td><td>3.7 ± 0.3</td></tr><tr><th></th><td><i>S. frontalis frontalis</i></td><td>5</td><td>69.5 ± 2.8</td><td>19.4 ± 0.8</td><td>61.0 ± 4.0</td><td>8.3 ± 0.1</td><td>3.5 ± 0.0</td></tr><tr><th></th><td><i>S. f. hanieli</i></td><td>0</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th></th><td><i>S. piurae</i></td><td>1</td><td>68</td><td>21.7</td><td>61</td><td>8.8</td><td>3.2</td></tr><tr><th></th><td><i>S. ochracea</i></td><td>1</td><td>67</td><td>23.5</td><td>56</td><td>8.4</td><td>4.1</td></tr><tr><th>male</th><td><i>S. m. melanotis</i></td><td>2</td><td>75.0 ± 2.8</td><td>19.5 ± 0.1</td><td>63.0 ± 5.7</td><td>8.4 ± 0.4</td><td>4.1 ± 0.4</td></tr><tr><th></th><td><i>S. m. castaneicollis</i></td><td>6</td><td>69.3 ± 1.5</td><td>21.1 ± 1.4</td><td>60.0 ± 1.8</td><td>7.8 ± 0.5</td><td>3.7 ± 0.2</td></tr><tr><th></th><td><i>S. f. frontalis</i></td><td>6</td><td>73.7 ± 3.4</td><td>19.4 ± 1.4</td><td>62.7 ± 2.4</td><td>8.5 ± 0.1</td><td>3.5 ± 0.1</td></tr><tr><th></th><td><i>S. f. hanieli</i></td><td>1</td><td>70</td><td>19.9</td><td>–</td><td>8.5</td><td>3.5</td></tr><tr><th></th><td><i>S. piurae</i></td><td>3</td><td>70.0 ± 0.0</td><td>21.9 ± 1.5</td><td>63.3 ± 5.8</td><td>8.7 ± 0.0</td><td>3.4 ± 0.1</td></tr><tr><th></th><td><i>S. ochracea</i></td><td>3</td><td>72.5 ± 0.7</td><td>22.2 ± 0.1</td><td>60.5 ± 0.7</td><td>9.1 ± 0.0</td><td>4.2 ± 0.0</td></tr></tbody></table>
Table 2. Pairwise uncorrected p - distances for 16 S in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships
<p><b>Table 2.</b> Pairwise uncorrected <i>p</i> -distances for 16S rRNA between <i>Petracola</i> species. The asterisk (*) indicates type locality.</p><table><tbody><tr><th></th><th>1</th><th>2</th><th>3</th><th>4</th><th>5</th><th>6</th><th>7</th><th>8</th><th>9</th><th>10</th></tr></tbody><tbody><tr><th>(1) <i>P. ventrimaculatus</i> CORBIDI 9235</th><td>-</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>(2) <i>P. ventrimaculatus</i> KU 219838</th><td>0.024</td><td>-</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>(3) <i>P. waka</i> KU 212687</th><td>0.063</td><td>0.071</td><td>-</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>(4) <i>P. waka</i> MUBI 2603</th><td>0.073</td><td>0.091</td><td>0.063</td><td>-</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>(5) <i>P. waka</i> MUBI 2605</th><td>0.073</td><td>0.091</td><td>0.063</td><td>0.000</td><td>-</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>(6) <i>P. waka</i> MUBI 2609*</th><td>0.069</td><td>0.082</td><td>0.066</td><td>0.031</td><td>0.031</td><td>-</td><td></td><td></td><td></td><td></td></tr><tr><th>(7) <i>P. waka</i> MUBI 2611*</th><td>0.069</td><td>0.082</td><td>0.066</td><td>0.031</td><td>0.031</td><td>0.000</td><td>-</td><td></td><td></td><td></td></tr><tr><th>(8) <i>P. shurugojalcapi</i> MUBI 17727</th><td>0.058</td><td>0.074</td><td>0.080</td><td>0.079</td><td>0.079</td><td>0.079</td><td>0.079</td><td>-</td><td></td><td></td></tr><tr><th>(9) <i>P. shurugojalcapi</i> PFAUNA 430</th><td>0.058</td><td>0.074</td><td>0.080</td><td>0.079</td><td>0.079</td><td>0.079</td><td>0.079</td><td>0.000</td><td>-</td><td></td></tr><tr><th>(10) <i>P. amazonensis</i> MUBI 11473</th><td>0.057</td><td>0.072</td><td>0.085</td><td>0.078</td><td>0.078</td><td>0.072</td><td>0.072</td><td>0.037</td><td>0.037</td><td>-</td></tr></tbody></table>
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>
Neutral-current DIS event samples at leading order with $E_e = 27.5\,{\rm GeV}$, $E_p = 920\,{\rm GeV}$, and $\mu_{\rm F}^2 = \mu_{\rm R}^2 = Q^2$
<p>Neutral-current DIS multi-jet event samples at parton level in the HDF5 event format.</p> <p>Beam energies: $E_e = 27.5\,{\rm GeV}$, $E_p = 920\,{\rm GeV}$</p> <p>Renormalisation and factorisation scale: $\mu_{\rm F}^2 = \mu_{\rm R}^2 = Q^2$ with seven-point scale variation</p> <p>PDF: NNPDF40_lo_pch_as_01180</p> <p>Generation cuts: $Q^2 > 2\,{\rm GeV}^2$, $k_{\rm T} > 2\,{\rm GeV}$ in the $k_{\rm T}$-algorithm with $D=1.0$</p> <p>Generated with <a href="https://gitlab.com/hpcgen/me" target="_blank" rel="noopener">Sherpa</a> using the run cards below.</p>
Neutral-current DIS event samples at leading order with $E_e = 27.5\,{\rm GeV}$, $E_p = 820\,{\rm GeV}$, and $\mu_{\rm F}^2 = \mu_{\rm R}^2 = Q^2$
<p>Neutral-current DIS multi-jet event samples at parton level in the HDF5 event format.</p> <p>Beam energies: $E_e = 27.5\,{\rm GeV}$, $E_p = 820\,{\rm GeV}$</p> <p>Renormalisation and factorisation scale: $\mu_{\rm F}^2 = \mu_{\rm R}^2 = Q^2$ with seven-point scale variation</p> <p>PDF: NNPDF40_lo_pch_as_01180</p> <p>Generation cuts: $Q^2 > 2\,{\rm GeV}^2$, $k_{\rm T} > 2\,{\rm GeV}$ in the $k_{\rm T}$-algorithm with $D=1.0$</p> <p>Generated with <a href="https://gitlab.com/hpcgen/me" target="_blank" rel="noopener">Sherpa</a> using the run cards below.</p>
The P-V-T dataset of liquid Fe-C alloys from FP-MD simulations
<p>The <em>P</em>-<em>V</em>-<em>T</em> dataset of liquid Fe-C alloys with different carbon contents (<em>X</em><sub>C</sub> = 0, 2.1, 4.7, 7.6, and 11.2 wt%) under the <em>P</em>-<em>T</em> conditions of the outer core (~136-330 GPa, 4000-6000 K) are obtained via first-principles molecular dynamics simulations.</p>
P-demotion: Extended sample
<p>This dataset is a component of the Polonez Bis project No. 2021/43/P/HS2/01395, co-funded by the National Science Centre and the European Union's Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement no. 945339, headed by Katarzyna Janic as Principle Investigator, from October 1, 2022, to September 30, 2024, at Adam Mickiewicz University. Katarzyna Janic and Krzysztof Strońsk created the dataset. They and Mohammad Tavakoli, Ph.D assistant, subsequently populated it. They entered data gathered through grammar mining. If necessary, they also contacted language experts for further clarification. This dataset corresponds to the <em>Extended sample </em>in Polonez Bis 1 project and is subject to further adjustment. Should you observe any inconsistency, please contact Katarzyna Janic at Katarzyna.Janic@amu.edu.pl.</p>
Validation of urine p-cresol glucuronide as renal cell carcinoma non-invasive biomarker
<p><strong>Description of the study</strong>: Renal cell carcinoma (RCC) stands among the most lethal urological malignancies. Most RCCs are incidentally diagnosed as initial symptoms are unspecific. Novel, minimally-invasive diagnostic and prognostic methods for RCC are needed, ideally in urine.</p> <p>Using UPLC-Q-ToF MS untargeted metabolomic analysis in urine, we previously revealed p-cresol glucuronide as potential RCC diagnostic marker. Additionally, urine samples one-year post-nephrectomy revealed isobutyryl-L-carnitine and L-proline betaine as potential RCC prognostic markers. Our present aim was to validate these differences in an independent cohort of RCC patients and healthy controls to strengthen their value as non-invasive biomarkers.</p> <p>In an independent cohort of 69 RCC patients and 52 controls we validated an increase in p-cresol glucuronide in urine from patients at diagnosis compared to controls (<em>P</em>=0.0043). It remained increased one-year post-nephrectomy (<em>P</em>=0.0288). The value of p-cresol glucuronide for RCC diagnosis was assessed with ROC curves analysis (AUC=0.66, 95% Confidence Interval 0.56-0.76). The role of isobutyryl-L-carnitine and <a name="_Hlk172707445"></a>L-proline betaine as prognostic markers could not be validated and will require a larger cohort.</p> <p>Our findings confirm the value of p-cresol glucuronide in urine as diagnostic marker for RCC in an independent cohort. This non-invasive method holds promise for enhancing patient care by reducing the need for potentially risky diagnostic procedures. Further metaproteomics-oriented approaches towards the tyrosine oxidation pathway and microbiota metagenomics studies may promote a holistic management of RCC.</p> <p><strong>Description of the data:</strong></p> <p>We provided data in .d format adquired with Agilent.</p> <p> </p> <p> </p>
Data Appendix for Lack, P., "Using Word Analysis to Track the Evolution of Emotional Well-being in Nineteenth-Century Industrializing Britain", Historical Methods (forthcoming)
<p>This file contains the data associated with the publication Lack, P., "Using Word Analysis to Track the Evolution of Emotional Well-being in Nineteenth-Century Industrializing Britain", <em>Historical Methods</em> (forthcoming). It quantifies the trend in emotional well-being expressed in a corpus of British pamphlets published between 1800 and 1900. The first page of the excel document presents this key data on the trend in emotional well-being. Sheet 1A presents summary statistics on the trend in emotional well-being and its correlation with GDP per capita and real wages. </p>
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.