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Table 6 in A revised taxonomy and phylogeny of opalinids (Stramenopiles: Opalinata) inferred from the analysis of complete nuclear ribosomal DNA genes
<p><b>Table 6.</b> Number and proportion of shared short tandem repeats (STRs) in the rDNA of opalinids. For each species* the total number of STRs (T) and the proportion of STRs species specific (not shared with other sequences) (S)* STRs shared by species of the same genus (G)* and STRs shared by species of different genera (C) are given. Incomplete sequences (those lacking ≥100 bases at the 3 <i>ʹ</i> or 5 <i>ʹ</i> end) are shown in parentheses. Abbreviation: N/A* sequence not available.</p><table><tbody><tr><th><b>Species</b></th><th><b>SSU rDNA</b></th><th><b>ITS1</b></th><th><b>5.8S rDNA</b></th><th><b>ITS2</b></th><th><b>LSU rDNA</b></th></tr><tr><th><b>T</b></th><th><b>S</b></th><th><b>G</b></th><th><b>C</b></th><th><b>T</b></th><th><b>S</b></th><th><b>G</b></th><th><b>C</b></th><th><b>T</b></th><th><b>S</b></th><th><b>G</b></th><th><b>C</b></th><th><b>T</b></th><th><b>S</b></th><th><b>G</b></th><th><b>C</b></th><th><b>T</b></th><th><b>S</b></th><th><b>G</b></th><th><b>C</b></th></tr><tr><th>OPALINIDA</th></tr></tbody><tbody><tr><th>(<i>Protoopalina axonucleata</i>)</th><td>45</td><td>13.3</td><td>35.6</td><td>51.1</td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td></tr><tr><th>(<i>Protoopalina intestinalis</i>)</th><td>52</td><td>11.5</td><td>38.5</td><td>50.0</td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td></tr><tr><th><i>Protoopalina limnocharis</i></th><td>68</td><td>14.7</td><td>29.4</td><td>55.9</td><td>19</td><td>31.6</td><td>68.4</td><td>0</td><td>5</td><td>0.0</td><td>20.0</td><td>80.0</td><td>16</td><td>25.0</td><td>75.0</td><td>0.0</td><td>177</td><td>3.4</td><td>47.5</td><td>49.1</td></tr><tr><th><i>Protoopalina pingi</i></th><td>68</td><td>14.7</td><td>29.4</td><td>55.9</td><td>20</td><td>35.0</td><td>65.0</td><td>0</td><td>5</td><td>0.0</td><td>20.0</td><td>80.0</td><td>15</td><td>20.0</td><td>80.0</td><td>0.0</td><td>179</td><td>4.5</td><td>46.9</td><td>48.6</td></tr><tr><th><i>Zelleriella orientalis</i></th><td>95</td><td>0.0</td><td>41.0</td><td>59.0</td><td>22</td><td>0.0</td><td>95.5</td><td>4.5</td><td>9</td><td>0.0</td><td>33.3</td><td>66.7</td><td>23</td><td>0.0</td><td>91.3</td><td>8.7</td><td>203</td><td>3.5</td><td>23.6</td><td>72.9</td></tr><tr><th><i>Zelleriella</i> sp.</th><td>95</td><td>0.0</td><td>41.0</td><td>59.0</td><td>22</td><td>0.0</td><td>95.5</td><td>4.5</td><td>9</td><td>0.0</td><td>33.3</td><td>66.7</td><td>23</td><td>0.0</td><td>91.3</td><td>8.7</td><td>212</td><td>6.1</td><td>22.7</td><td>71.2</td></tr><tr><th><i>Opalina undulata</i></th><td>104</td><td>12.5</td><td>33.7</td><td>53.8</td><td>26</td><td>80.8</td><td>15.4</td><td>3.8</td><td>8</td><td>0.0</td><td>37.5</td><td>62.5</td><td>25</td><td>44.0</td><td>48.0</td><td>8.0</td><td>213</td><td>10.3</td><td>19.3</td><td>70.4</td></tr><tr><th><i>Opalina triangulata</i></th><td>103</td><td>11.6</td><td>34.0</td><td>54.4</td><td>24</td><td>79.1</td><td>16.7</td><td>4.2</td><td>8</td><td>0.0</td><td>37.5</td><td>62.5</td><td>26</td><td>46.2</td><td>46.2</td><td>7.6</td><td>207</td><td>7.7</td><td>19.8</td><td>72.5</td></tr><tr><th><i>Opalina obtrigonoidea</i></th><td>104</td><td>12.5</td><td>33.7</td><td>53.8</td><td>27</td><td>81.5</td><td>14.8</td><td>3.7</td><td>8</td><td>0.0</td><td>37.5</td><td>62.5</td><td>26</td><td>46.2</td><td>46.2</td><td>7.6</td><td>217</td><td>12.0</td><td>18.9</td><td>69.1</td></tr><tr><th><i>Opalina japonica</i></th><td>103</td><td>11.6</td><td>34.0</td><td>54.4</td><td>25</td><td>80.0</td><td>16.0</td><td>4.0</td><td>8</td><td>0.0</td><td>37.5</td><td>62.5</td><td>29</td><td>51.7</td><td>41.4</td><td>6.9</td><td>215</td><td>11.2</td><td>19.1</td><td>69.7</td></tr><tr><th><i>Opalina longa</i></th><td>105</td><td>13.4</td><td>33.3</td><td>53.3</td><td>20</td><td>75.0</td><td>20.0</td><td>5.0</td><td>8</td><td>0.0</td><td>37.5</td><td>62.5</td><td>25</td><td>44.0</td><td>48.0</td><td>8.0</td><td>213</td><td>10.3</td><td>19.3</td><td>70.4</td></tr><tr><th>PROTEROMONADIDA</th></tr><tr><th><i>Karotomorpha</i> sp. a*b</th><td>52</td><td>36.5</td><td></td><td>63.5</td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td></tr><tr><th><i>Proteromonas lacertae</i> b</th><td>56</td><td>41.1</td><td></td><td>58.9</td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td><td>N/A</td><td></td><td></td><td></td></tr></tbody></table><p><sup>aThe</sup> data presented correspond to the sequence with accession number DQ431242;the <i>Karotomorpha</i> sp. DQ431243 sequence is partial and has not been considered for this analysis.</p><p><sup>bData</sup> are available for only one species per genus;STRs are therefore considered in two categories* as species/genus specific* or as shared with other genera.</p>
Table 5 in A revised taxonomy and phylogeny of opalinids (Stramenopiles: Opalinata) inferred from the analysis of complete nuclear ribosomal DNA genes
<p><b>Table 5.</b> Types of short tandem repeats (STRs) found in the sequences from opalinids.</p><table><tbody><tr><th><b>Type</b></th><th><b>Characteristics</b></th><th><b>Example</b></th><th><b>Sequence (position)</b></th></tr></tbody><tbody><tr><th>Direct</th><td>Head to tail</td><td></td><td></td></tr><tr><th>Perfect</th><td>All units equal</td><td>TAATAATAATAATAA</td><td><i>Opalina undulata</i> MN 638758 (3423)</td></tr><tr><th>Imperfect</th><td>With substitutions and/or indels</td><td>AGTTT ATTTT AATTT</td><td><i>Zelleriella</i> sp. MN638763 (1762)</td></tr><tr><th>Overlapped</th><td>STR includes bases</td><td>TTTA[T ATTAT]/ [TAT TAT] TAT</td><td><i>Protoopalina limnocharis</i> MN 638759 (1493/1497)</td></tr><tr><th>Inverted</th><td>Head to head</td><td></td><td></td></tr><tr><th>Perfect</th><td>All units equal</td><td>TTTATAATATTT</td><td><i>Opalina triangulata</i> MN 638762 (470)</td></tr><tr><th>Imperfect</th><td>With substitutions and/or indels</td><td>TTATTATTATTATTTTTTTTATTA(-) TATTATT</td><td><i>Opalina japonica</i> MN 638764 (73)</td></tr></tbody></table>
Table 3. Principal component loading values for seven habitat variables across 13 in Impacts of Wastewater Effluent on Temperate Stream Fish Assemblage Structure
<p>Table 3. Principal component loading values for seven habitat variables across 13 sites.</p><table><tbody><tr><th>Variable</th><th>PC1</th><th>PC2</th><th>PC3</th><th>PC4</th><th>PC5</th><th>PC6</th><th>PC7</th></tr></tbody><tbody><tr><th>Mean depth</th><td>0.48071</td><td>0.28063</td><td>0.17675</td><td>0.44277</td><td>0.31253</td><td>0.60423</td><td>0.01098</td></tr><tr><th>Max depth</th><td>0.52734</td><td>0.2317</td><td>0.01965</td><td>0.21237</td><td>0.15811</td><td><i>–</i> 0.7713</td><td>0.05367</td></tr><tr><th>Discharge</th><td>0.1488</td><td>0.53788</td><td><i>–</i> 0.4311</td><td>0.37747</td><td><i>–</i> 0.599</td><td>0.02831</td><td><i>–</i> 0.0247</td></tr><tr><th>% gravel</th><td>0.52703</td><td><i>–</i> 0.0162</td><td><i>–</i> 0.1975</td><td><i>–</i> 0.5051</td><td><i>–</i> 0.3351</td><td>0.17973</td><td>0.53227</td></tr><tr><th>% pebble</th><td><i>–</i> 0.0551</td><td><i>–</i> 0.5723</td><td><i>–</i> 0.4095</td><td>0.52749</td><td>0.10692</td><td><i>–</i> 0.0208</td><td>0.46008</td></tr><tr><th>% cobble</th><td><i>–</i> 0.292</td><td>0.16769</td><td>0.66603</td><td>0.16685</td><td><i>–</i> 0.1803</td><td><i>–</i> 0.0806</td><td>0.61335</td></tr><tr><th>% boulder</th><td><i>–</i> 0.3204</td><td>0.47152</td><td><i>–</i> 0.3636</td><td><i>–</i> 0.2349</td><td>0.60197</td><td><i>–</i> 0.0034</td><td>0.35384</td></tr></tbody></table>
Table 1 in Impacts of Wastewater Effluent on Temperate Stream Fish Assemblage Structure
<p>Table 1. PERMANOVA table of results indicating a significant difference in fish assemblage structure between East and West Fork sites (<i>Pseudo-F</i> ¼ 10.481, df ¼ 1, <i>P</i> ¼ 0.0001) after accounting for the effect of the site distance covariate, which does influence fish assemblage structure (Pseudo- <i>F</i> ¼ 7.813, df ¼ 1, <i>P</i> ¼ 0.00015). Stream distance data (between sites) were square root transformed prior to analysis to ensure that distance variation of East and West Fork sites were more comparable.</p><table><tbody><tr><th><b>Source</b></th><th><b>df</b></th><th><b>SS</b></th><th><b>MS</b></th><th><b>Pseudo- <i>F</i></b></th><th><b><i>P</i> (perm)</b></th><th><b>Unique perms</b></th></tr></tbody><tbody><tr><th>Distance (covariate)</th><td>1</td><td>6650.8</td><td>6650.8</td><td>7.813</td><td>0.0001</td><td>9959</td></tr><tr><th>Site (East vs. West)</th><td>1</td><td>8921.9</td><td>8921.9</td><td>10.481</td><td>0.0001</td><td>9955</td></tr><tr><th>Res</th><td>23</td><td>19579</td><td>851.26</td><td></td><td></td><td></td></tr><tr><th>Total</th><td>25</td><td>35152</td><td></td><td></td><td></td><td></td></tr></tbody></table>
Table 4. Principal component loading values for the four substrate categories measured across all 26 in Impacts of Wastewater Effluent on Temperate Stream Fish Assemblage Structure
<p>Table 4. Principal component loading values for the four substrate categories measured across all 26 sites.</p><table><tbody><tr><th>Variables</th><th>PC1</th><th>PC2</th><th>PC3</th><th>PC4</th></tr></tbody><tbody><tr><th>% gravel</th><td>0.63444</td><td>0.50857</td><td>0.10028</td><td>0.5734</td></tr><tr><th>% pebble</th><td>0.20598</td><td><i>–</i> 0.8296</td><td><i>–</i> 0.0496</td><td>0.51658</td></tr><tr><th>% cobble</th><td><i>–</i> 0.6728</td><td>0.13769</td><td>0.49052</td><td>0.53647</td></tr><tr><th>% boulder</th><td><i>–</i> 0.3201</td><td>0.18476</td><td><i>–</i> 0.8642</td><td>0.3414</td></tr></tbody></table>
Table 4. Posterior means and 95 in A revised taxonomy and phylogeny of opalinids (Stramenopiles: Opalinata) inferred from the analysis of complete nuclear ribosomal DNA genes
<p><b>Table 4.</b> Posterior means and 95% credibility intervals (CIs) of divergence times (DTs) of Opalinata lineages (in million years) inferred in the TimeTree analysis. Three groups of calibration time points were used to calibrate the molecular clock. Group A (‘sequence evolution’): calibration points with uniform distribution were assigned for the origin of Stramenopiles (1469.6–812.4 Mya) and Ciliophora (1344.0–627.3 Mya) and to the split of Apicomplexa and Dinoflagellata (1098.8–501.9 Mya). Group B (‘host class constraints’): the maximum bounds of the origin of Amphibia (355.7 Mya) and Sauropsida (322.4 Mya) were assigned to the nodes where <i>Karotomorpha</i> (parasite of amphibians) and <i>Proteromonas</i> (parasite of lizards) branched off* respectively. Group C (‘anuran family constraints’): a maximum bound was assigned to the nodes where <i>Protoopalina</i> * <i>Zelleriella</i> * and <i>Opalina</i> branched off* based on the estimated maximum time of emergence of the most ancient anuran family in which species of each genus have been cited (respectively: Ascaphidae * 204 Mya; Microhylidae * 116.3 Mya; Bombinatoridae and Alytidae * 196 Mya). Four scenarios were analysed by combining the groups of calibration time points.</p><table><tbody><tr><th></th><th><b>Scenario 1 (A)</b></th><th><b>Scenario 2 (A + B)</b></th><th><b>Scenario 3 (A + C)</b></th><th><b>Scenario 4 (A + B + C)</b></th></tr></tbody><tbody><tr><th></th><td><b>DT (95% CI)</b></td><td><b>DT (95% CI)</b></td><td><b>DT (95% CI)</b></td><td><b>DT (95% CI)</b></td></tr><tr><th>Opalinata</th><td>586.7 (304.6–1130.1)</td><td>515.7 (267.0–996.0)</td><td>586.7 (304.6–1129.8)</td><td>515.7 (267.0–996.1)</td></tr><tr><th><i>Karotomorpha</i></th><td>351.7 (165.2–748.8)</td><td>309.2 (178.8–355.7)</td><td>351.7 (165.6–746.9)</td><td>309.2 (178.8–355.7)</td></tr><tr><th>Opalinida</th><td>250.4 (110.7–566.5)</td><td>220.1 (119.3–286.8)</td><td>250.4 (112.2–558.6)</td><td>220.1 (119.3–286.8)</td></tr><tr><th><i>Protoopalina</i></th><td>119.4 (48.6–293.5)</td><td>105.0 (56.1–196.6)</td><td>119.4 (55.1–204.0)</td><td>105.0 (56.0–196.9)</td></tr><tr><th><i>Zelleriella – Opalina</i> split</th><td>49.7 (17.4–142.3)</td><td>43.7 (20.1–95.0)</td><td>49.7 (19.8–124.7)</td><td>43.7 (20.4–93.5)</td></tr></tbody></table>
Table 4 in Courtship and Mating Behavior of the Rare, Rock-Crevice Dwelling Salamander Plethodon petraeus with a Review for Eastern North American Woodland Salamanders (Amphibia: Plethodontidae)
<p><b>Table 4. Pearson Product Moment correlation coefficients between the duration and frequency of some behaviors during the preliminary (pre-TSW) phase of courtship in the salamander <i>Plethodon petraeuS</i>. Data are from 20 individually unique pairs that engaged in ten incomplete courtships, which did not proceed to a tail-straddling walk (TSW), and ten complete courtships with TSW and spermatophore deposition. Duration <i>¼</i> minutes per pre-TSW hour. Frequency <i>¼</i> occurrences per pre-TSW hour. Apart <i>¼</i> periods when salamanders were more than about 2.5 cm apart after their initial encounter. Close <i>¼</i> periods when salamanders were within about 2.5 cm of each other but not in sustained contact via the mental gland. Dance/shuffle <i>¼</i> foot dance and foot shuffle. MG <i>¼</i> mental gland. See text for description of behaviors. C Coefficient for complete courtships, I coefficient for incomplete courtships, A coefficient for all courtships when both incomplete and complete courtships had very similar correlations. * <i>P</i></b>, <b>0.02, ** <i>P</i></b>, <b>0.01, *** <i>P</i></b>, 0.001.</p><table><tbody><tr><th><b>Duration of period or behavior</b></th></tr></tbody><tbody><tr><th></th><td><b>Apart</b></td><td><b>Close</b></td><td><b>MG</b></td><td><b>Discontinuous,</b> <b>female-first TSW</b></td><td><b>Continuous,</b> <b>female-first TSW</b></td></tr><tr><th></th><td><b>(</b>. <b>2.5 cm)</b></td><td><b>(2.5 cm)</b></td><td><b>sliding</b></td></tr><tr><th>Male frequency</th><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Dance/shuffle</th><td></td><td>I 0.922***</td><td>A 0.528*</td><td></td><td>I 0.734*</td></tr><tr><th>MG popping</th><td></td><td></td><td></td><td></td><td>I 0.748*</td></tr><tr><th>MG swipe</th><td></td><td></td><td></td><td>C 0.704*</td><td></td></tr><tr><th>Mouth grasp</th><td>I 0.856**</td><td></td><td></td><td></td><td></td></tr><tr><th>Snout under</th><td></td><td></td><td></td><td>A 0.595**</td><td></td></tr><tr><th>Female frequency</th><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Tail flex</th><td>I 0.806**</td><td></td><td></td><td></td><td></td></tr><tr><th>Undulate tail</th><td></td><td></td><td>A 0.751***</td><td></td><td></td></tr></tbody></table>
Table 2 in Impacts of Wastewater Effluent on Temperate Stream Fish Assemblage Structure
<p>Table 2. Similarity percentage (SIMPER) showing species contributions (Contrib%) to dissimilarity between East and West Fork sites. West and East Fork average abundance (Av.Abund) columns list the transformed mean abundances for species in both forks, ‘Diss/SD’ represents the ratio between the average dissimilarity and standard deviation, and the cumulative % (Cum.%) column lists the cumulative dissimilarity across species with a 90% cutoff. The average dissimilarity between the East and West Forks was 58.74%.</p><table><tbody><tr><th><b>Species</b></th><th><b>West Fork</b> <b>Av.Abund</b></th><th><b>East Fork</b> <b>Av.Abund</b></th><th></th><th></th><th></th><th></th></tr><tr><th><b>Av.Diss</b></th><th><b>Diss/SD</b></th><th><b>Contrib%</b></th><th><b>Cum.%</b></th></tr></tbody><tbody><tr><th><i>Etheostoma spectabile</i></th><td>4.38</td><td>2.34</td><td>13.7</td><td>1.53</td><td>23.32</td><td>23.32</td></tr><tr><th><i>Etheostoma flabellare</i></th><td>0</td><td>2.26</td><td>11.97</td><td>1.73</td><td>20.38</td><td>43.7</td></tr><tr><th><i>Chrosomus erythrogaster</i></th><td>1.36</td><td>0.24</td><td>6.23</td><td>0.78</td><td>10.61</td><td>54.3</td></tr><tr><th><i>Noturus exilis</i></th><td>0.32</td><td>1.15</td><td>6.16</td><td>1.19</td><td>10.49</td><td>64.79</td></tr><tr><th><i>Cottus bairdii</i></th><td>1.32</td><td>1.72</td><td>5.97</td><td>1.27</td><td>10.17</td><td>74.96</td></tr><tr><th><i>Campostoma</i> sp.</th><td>1.15</td><td>0.45</td><td>5.62</td><td>1.18</td><td>9.57</td><td>84.54</td></tr><tr><th><i>Luxilus zonatus</i></th><td>0.71</td><td>0.2</td><td>3.82</td><td>0.84</td><td>6.51</td><td>91.05</td></tr></tbody></table>
Table 3 in Courtship and Mating Behavior of the Rare, Rock-Crevice Dwelling Salamander Plethodon petraeus with a Review for Eastern North American Woodland Salamanders (Amphibia: Plethodontidae)
<p><b>Table 3. Pearson Product Moment correlation coefficients between the frequency of some male and female behaviors (i.e., occurrences per hour for each pair) during the preliminary (pre-TSW) phase of courtship in the salamander <i>Plethodon petraeuS</i>. Data are from 20 individually unique pairs that engaged in ten incomplete courtships, which did not proceed to a tail-straddling walk (TSW), and ten complete courtships with TSW and spermatophore deposition. Dance/shuffle <i>¼</i> foot dance and foot shuffle. MG <i>¼</i> mental gland. See text for description of behaviors. C Coefficient for complete courtships, I coefficient for incomplete courtships, A coefficient for all courtships when both incomplete and complete courtships had very similar correlations. * <i>P</i></b>, <b>0.025, ** <i>P</i></b>, <b>0.015, *** <i>P</i></b>, 0.001.</p><table><tbody><tr><th></th><th><b>Male behavior</b></th><th><b>Female behavior</b></th></tr><tr><th></th><th><b>Mouth</b> <b>grasp</b></th><th><b>Position</b> <b>for TSW</b></th><th><b>Undulate</b> <b>tail</b></th><th><b>Turn</b> <b>back</b></th></tr></tbody><tbody><tr><th>Male behavior</th><td></td><td></td><td></td><td></td></tr><tr><th>Dance/shuffle</th><td></td><td>A 0.773***</td><td>A 0.660**</td><td></td></tr><tr><th>Snout under</th><td></td><td>I 0.824**</td><td></td><td></td></tr><tr><th>MG popping</th><td></td><td></td><td>A 0.548**</td><td></td></tr><tr><th>Female behavior</th><td></td><td></td><td></td><td></td></tr><tr><th>Tail flex</th><td>I 0.801**</td><td></td><td></td><td></td></tr><tr><th>Undulate tail</th><td></td><td>A 0.507*</td><td></td><td>C 0.762**</td></tr><tr><th>Chin over</th><td></td><td>A 0.566**</td><td>C 0.793**</td><td>A 0.912***</td></tr></tbody></table>
Table 2 in Courtship and Mating Behavior of the Rare, Rock-Crevice Dwelling Salamander Plethodon petraeus with a Review for Eastern North American Woodland Salamanders (Amphibia: Plethodontidae)
<p><b>Table 2. Duration (min) of behaviors and phases during courtship and mating in the salamander <i>Plethodon petraeuS</i>. Data are from ten individually unique pairs that engaged in complete courtship with tail-straddling walk (TSW) and spermatophore deposition. For Pair 3 courtship, there were two spermatophore depositions. (A) Apart <i>¼</i> periods when salamanders were more than about 2.5 cm apart after their initial encounter. (B) Close <i>¼</i> periods when salamanders were within about 2.5 cm of each other but not in sustained contact via the mental gland (e.g., includes periods with male foot dance/shuffle, undulate tail, mental-gland tap/swipe, nudge, and snout under). (C) Sliding <i>¼</i> mental-gland sliding. (D) ffTSWd <i>¼</i> discontinuous, female-first TSW. (E) ffTSWc <i>¼</i> continuous, female-first TSW. (F) upTSW <i>¼</i> unsuccessful position for TSW. (G) spTSW <i>¼</i> successful position for TSW. (H) TSW <i>¼</i> tail-straddling walk. (I) SD <i>¼</i> spermatophore deposition. (J) LOS <i>¼</i> lead female over spermatophore. (K) POC <i>¼</i> position on sperm cap. *Successful retrieval of sperm cap. Total B to G <i>¼</i> duration of pre-TSW phase of courtship. Total B to K <i>¼</i> total duration of pre-TSW phase, TSW, and sperm transfer. Total A to K <i>¼</i> total duration of courtship from the initial encounter between salamanders until the final attempted retrieval of sperm cap. Pearson Product Moment correlation coefficients (which do not include durations for behaviors from the second courtship sequence for pair 3): 1 r <i>¼</i> 0.952, <i>P</i></b>, <b>0.0001 for Apart and TSW; 2 r <i>¼</i> 0.770, <i>P</i></b>, <b>0.01 for Sliding and ffTSWd; 3 r <i>¼</i> 0.964, <i>P</i></b>, <b>0.00001 for Sliding and upTSW; 4 r <i>¼</i> 0.765, <i>P</i></b>, 0.01 for ffTSWd and upTSW.</p><table><tbody><tr><th></th><th><b>Pre-TSW phase</b></th><th><b>TSW & sperm-transfer phase</b></th></tr><tr><th></th><th><b>(A)</b> <b>1</b></th><th><b>(B)</b></th><th><b>(C)</b> <b>2,3</b></th><th><b>(D)</b> <b>2,4</b></th><th><b>(E)</b></th><th><b>(F)</b> <b>3,4</b></th><th><b>(G)</b></th><th><b>(H)</b> <b>1</b></th><th><b>(I)</b></th><th><b>(J)</b></th><th><b>(K)</b></th><th><b>Total</b></th><th><b>Total</b></th><th><b>Total</b></th></tr><tr><th><b>Pair</b></th><th><b>Apart</b></th><th><b>Close</b></th><th><b>Sliding</b></th><th><b>ffTSWd</b></th><th><b>ffTSWc</b></th><th><b>upTSW</b></th><th><b>spTSW</b></th><th><b>TSW</b></th><th><b>SD</b></th><th><b>LOS</b></th><th><b>POC</b></th><th><b>B to G</b></th><th><b>B to K</b></th><th><b>A to K</b></th></tr></tbody><tbody><tr><th>1</th><td>29</td><td>152</td><td>5</td><td>3</td><td>0</td><td>3</td><td>3</td><td>31</td><td>7</td><td>0.4</td><td>0.5*</td><td>166</td><td>204.9</td><td>233.9</td></tr><tr><th>2</th><td>13</td><td>122</td><td>3</td><td>20</td><td>0</td><td>2</td><td>6</td><td>22</td><td>8</td><td>0.3</td><td>0.4*</td><td>153</td><td>183.7</td><td>196.7</td></tr><tr><th>3</th><td>9</td><td>69</td><td>19</td><td>3</td><td>0</td><td>73</td><td>2</td><td>23</td><td>7</td><td>0.4</td><td>0.8</td><td>166</td><td>197.2</td><td></td></tr><tr><th></th><td>2</td><td>66</td><td>3</td><td>0</td><td>0</td><td>17</td><td>5</td><td>26</td><td>8</td><td>0.6</td><td>0.5*</td><td>91</td><td>126.1</td><td>334.3</td></tr><tr><th>4</th><td>71</td><td>24</td><td>9</td><td>0</td><td>0</td><td>3</td><td>3</td><td>42</td><td>7</td><td>0.3</td><td>0.5*</td><td>39</td><td>88.8</td><td>159.8</td></tr><tr><th>5</th><td>172</td><td>45</td><td>35</td><td>26</td><td>170</td><td>35</td><td>12</td><td>223</td><td>9</td><td>0.3</td><td></td><td>323</td><td>555.3</td><td>727.3</td></tr><tr><th>6</th><td>12</td><td>69</td><td>33</td><td>6</td><td>0</td><td>17</td><td>15</td><td>20</td><td>8</td><td>0.4</td><td>0.8</td><td>140</td><td>169.2</td><td>181.2</td></tr><tr><th>7</th><td>8</td><td>36</td><td>33</td><td>7</td><td>0</td><td>42</td><td>1</td><td>26</td><td>8</td><td>0.3</td><td>0.7</td><td>119</td><td>154</td><td>162</td></tr><tr><th>8</th><td>29</td><td>119</td><td>68</td><td>15</td><td>0</td><td>73</td><td>10</td><td>43</td><td>7</td><td>0.5</td><td>0.6</td><td>285</td><td>336.1</td><td>365.1</td></tr><tr><th>9</th><td>8</td><td>323</td><td>48</td><td>32</td><td>0</td><td>88</td><td>12</td><td>32</td><td>6</td><td>0.4</td><td>0.9*</td><td>503</td><td>542.3</td><td>550.3</td></tr><tr><th>10</th><td>33</td><td>184</td><td>210</td><td>46</td><td>0</td><td>270</td><td>5</td><td>30</td><td>8</td><td>0.4</td><td>0.6*</td><td>715</td><td>754</td><td>787</td></tr><tr><th>Total</th><td>386</td><td>1209</td><td>466</td><td>158</td><td>170</td><td>623</td><td>74</td><td>518</td><td>83</td><td>4.3</td><td>6.3</td><td>2700</td><td>3311.6</td><td>3697.6</td></tr><tr><th>Mean</th><td>35.1</td><td>109.9</td><td>42.4</td><td>14.4</td><td>15.5</td><td>56.6</td><td>6.7</td><td>47.1</td><td>7.5</td><td>0.4</td><td>0.6</td><td>245.5</td><td>301.1</td><td>369.8</td></tr><tr><th>SD</th><td>49.4</td><td>86.7</td><td>59.3</td><td>15.1</td><td>51.3</td><td>77.2</td><td>4.7</td><td>58.8</td><td>0.8</td><td>0.1</td><td>0.2</td><td>202.3</td><td>218.6</td><td>237.3</td></tr><tr><th>% Total</th></tr><tr><th>B to G</th><td></td><td>44.8</td><td>17.3</td><td>5.9</td><td>6.3</td><td>23.1</td><td>2.7</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>% Total</th></tr><tr><th>B to K</th><td></td><td>36.5</td><td>14.1</td><td>4.8</td><td>5.1</td><td>18.8</td><td>2.2</td><td>15.6</td><td>2.5</td><td>0.1</td><td>0.2</td><td></td><td></td><td></td></tr><tr><th>% Total</th></tr><tr><th>A to K</th><td>10.4</td><td>32.7</td><td>12.6</td><td>4.3</td><td>4.6</td><td>16.8</td><td>2.0</td><td>14.0</td><td>2.2</td><td>0.1</td><td>0.2</td><td></td><td></td><td></td></tr></tbody></table>
TABLE 1 in Ground beetles of the subfamily Lebiinae (Carabidae) of Guinea-Bissau: description of three new species and faunistic notes
<p><b>TABLE 1.</b> List of species and subspecies of Lebiinae sampled in different localities during the entomological mission to Guinea-Bissau in 2009. For each locality is (are) indicated the sampled date(s). * New species records for Guinea-Bissau. ** Endemic species of Guinea-Bissau.</p><table><tbody><tr><th><b>Species/subspecies</b></th><th><b>Localities (dates)</b></th></tr><tr><th><b>Cacheu (IBAP)</b> (25- 28.VI.2009)</th><th><b>Banhinda</b> (26- 27.VI.2009)</th><th><b>Béli</b> (3- 5.VII.2009)</th><th><b>Jemberem (IBAP)</b> (09.VII.2009)</th><th><b>Jemberem (Canamina)</b> (09.VII.2009)</th><th><b>Jemberem (Lautchandé)</b> (12.VII.2009)</th><th><b>Indjassen (P.N.L.Cufada)</b> (16.VII.2009)</th><th><b>Nhala- Incansolé (P.N.L.Cufada)</b> (17.VII.2009)</th><th><b>Quinhamel</b> (21- 23.VII.2009)</th></tr></tbody><tbody><tr><th><b>*</b> <i>Tetragonoderus</i> (<i>Tetragonoderus</i>) <i>quadrum</i></th><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Tetragonoderus</i> (<i>Tetragonoderus</i>) <i>viridicollis</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Anaulacus</i> (<i>Caphora</i>) <i>africanus</i></th><td></td><td></td><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>* Somoplatus amplicollis</i></th><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>*</b> <i>Somoplatus fulvus</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>+</td><td>+</td><td></td></tr><tr><th><b>*</b> <i>Anomotarus</i> (<i>Dromiotes</i>) <i>maculipennis</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Paraglycia rufula</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Cymindoidea bisignata</i></th><td></td><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Cylindrocranius risbeci ganganus</i></th><td></td><td></td><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Polyaulacus brunneus</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Lebia</i> (<i>Lebia</i>) <i>garambae</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Lebia</i> (<i>Nematopeza</i>) <i>melanura</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td>+</td><td>+</td><td></td></tr><tr><th><i>Lebia</i> (<i>Nematopeza</i>) <i>verisimilis</i></th><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td><td></td><td></td></tr><tr><th><b>*</b> <i>Parena africana</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>+</td><td>+</td><td></td></tr><tr><th><i>Peliocypas debilis</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Arsinoe flavosignata</i></th><td></td><td></td><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Arsinoe laevigata</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td></tr><tr><th><b>*</b> <i>Arsinoe triguttata</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Catascopus</i> (<i>Catascopus</i>) <i>senegalensis</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>**</b> <i>Dontolobus bivari</i> n. sp.</th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>* Lobodontus compressus</i></th><td></td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Lobodontus trimaculatus</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Archicolliuris dimidiata</i></th><td>+</td><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><b>**</b> <i>Lasiocera schwarzi</i> sp. n.</th><td>+</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Odacantha</i> (<i>Neocolliuris</i>) <i>cyanea</i></th><td></td><td></td><td></td><td>+</td><td></td><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Smeringocera lineola</i></th><td>+</td><td>+</td><td>+</td><td>+</td><td></td><td></td><td></td><td></td><td>+</td></tr><tr><th><i>Smeringocera nigeriana nigeriana</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Stenidia corrusca</i></th><td></td><td></td><td></td><td></td><td>+</td><td></td><td>+</td><td></td><td></td></tr><tr><th><i>Pentagonica elegans</i></th><td></td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td><td>+</td></tr><tr><th><b>*</b> <i>Perigona</i> (<i>Euripogena</i>) <i>congoana</i></th><td></td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td><td></td></tr><tr><th><b>*</b> <i>Perigona</i> (<i>Perigona</i>) <i>pallida</i></th><td></td><td></td><td></td><td></td><td></td><td>+</td><td></td><td></td><td></td></tr><tr><th>Total</th><td>5</td><td>12</td><td>2</td><td>5</td><td>2</td><td>3</td><td>10</td><td>3</td><td>2</td></tr></tbody></table><p>......Continued on the next page</p>
Myeloid NCOA4 Table S2 and S3
Open the record for dataset details and reuse information.
Table 2 in The atyid shrimp (Crustacea: Decapoda: Atyidae) rostrum: phylogeny versus adaptation, taxonomy versus trophic ecology
<p>Table 2. List of the untransformed morphometric characters and their ratios.</p><table><tbody><tr><th>Morphometric character</th><th>Ratio</th><th></th><th>Formula</th></tr></tbody><tbody><tr><th>CL</th><td>postorbital carapace length</td><td></td><td></td><td></td></tr><tr><th>RO</th><td>rostral length</td><td>rcl</td><td>relative rostral length</td><td>RO/CL</td></tr><tr><th>CT</th><td>length of part of the</td><td>ctcl</td><td>relative length of part</td><td>CT/CL</td></tr><tr><th></th><td>carapace with teeth</td><td></td><td>of the carapace with</td><td></td></tr><tr><th></th><td>behind the eyes</td><td></td><td>teeth behind the eyes</td><td></td></tr><tr><th><i>ROT1</i></th><td>number of dorsal teeth on</td><td>r12rct</td><td>density of dorsal teeth</td><td>(<i>ROT1</i> + <i>ROT2</i>)</td></tr><tr><th></th><td>rostrum in front of the eyes</td><td></td><td>on rostrum and</td><td>/(RO+CT)</td></tr><tr><th><i>ROT2</i></th><td>number of teeth on carapace</td><td></td><td>carapace</td><td></td></tr><tr><th>behind the eyes</th></tr><tr><th><i>ROT3</i></th><td>number of ventral teeth on</td><td>r3r</td><td>density of ventral teeth</td><td><i>ROT3</i> /RO</td></tr><tr><th></th><td>rostrum</td><td></td><td>on rostrum</td><td></td></tr></tbody></table><p>Numerical counted characters are written in italics.</p>
TABLE 1 in Compsoneura nallarettiana (Myristicaceae), a new species from north-western Peru
<p><b>TABLE 1.</b> Comparison of <i>Compsoneura nallarettiana</i> with similar species.</p><table><tbody><tr><th>Species</th><th><i>Compsoneura cuatrecasasii</i></th><th><i>Compsoneura debilis</i></th><th><i>Compsoneura diazii</i></th><th><i>Compsoneura excelsa</i></th><th><i>Compsoneura mutisii</i></th><th><i>Compsoneura nallarettiana</i></th></tr></tbody><tbody><tr><th>Leaf base</th><td>rounded or broadly obtuse</td><td>attenuate</td><td>acute</td><td>acute to attenuate</td><td>acute to attenuate</td><td>acute to attenuate</td></tr><tr><th>Leaf apex</th><td>obtuse or obtusely cuspidate</td><td>rounded or obtuse</td><td>acute to caudate</td><td>acuminate short to cuspidate</td><td>acuminate to obtuse</td><td>acuminate to brevi-acuminate</td></tr><tr><th>Staminate inflorescence length (cm)</th><td>1.5–2.5</td><td><1.5</td><td>4.0–4.5</td><td>4.0–9.0</td><td>2.0</td><td>(5.5-) 6.5–10.4</td></tr><tr><th>Number of flowers per branch in staminate inflorescences</th><td>3–5</td><td>5–20</td><td>2–6</td><td>2–3</td><td>3–5</td><td>2–8</td></tr><tr><th>Staminate flower tube length (cm)</th><td>0.120–0.140</td><td>0.100</td><td>0.900–0.130</td><td>No information</td><td>No information</td><td>0.028–0.088</td></tr><tr><th>Androecium length (cm)</th><td>0.15</td><td>0.10</td><td>0.10–0.14</td><td>0.12</td><td>0.10</td><td>0.05–0.12</td></tr><tr><th>Anther length (cm)</th><td>0.30–0.40</td><td>0.06–0.08</td><td>0.09–0.12</td><td>0.08–0.11</td><td>0.05–0.06</td><td>0.03–0.08</td></tr><tr><th>Fruit</th><td>pedunculate</td><td>pedunculate</td><td>pedunculate</td><td>pedunculate</td><td>pedunculate</td><td>sessile</td></tr><tr><th>Distribution</th><td>Colombia</td><td>Brazil, Colombia and Venezuela</td><td>Peru and Ecuador</td><td>Costa Rica</td><td>Ecuador and Colombia</td><td>Peru</td></tr></tbody></table>
TABLE 1 in A new species of Macrobrachium (Decapoda, Palaemonidae) from Vamanapuram River, Southern Kerala, India
<p><b>TABLE 1.</b> Morphometric and meristic features of <i>Macrobrachium prabhakarani</i> <b>sp. nov.</b> (length in mm and weight in g.)</p><table><tbody><tr><th>Specimen nos.</th><th>1</th><th>2</th><th>3</th><th>4</th><th>5</th><th>6</th><th>7</th></tr></tbody><tbody><tr><th>Total length</th><td>42</td><td>41</td><td>37</td><td>41</td><td>43</td><td>25</td><td>26</td></tr><tr><th>Carapace length</th><td>13</td><td>11</td><td>11</td><td>13</td><td>13</td><td>7</td><td>8</td></tr><tr><th>Length of rostrum</th><td>7</td><td>6</td><td>6</td><td>7</td><td>7</td><td>4</td><td>5</td></tr><tr><th>Max. width of carapace</th><td>7.5</td><td>7.0</td><td>7.0</td><td>7.5</td><td>7.0</td><td>6.0</td><td>5.0</td></tr><tr><th>Preorbital teeth</th><td>7</td><td>7</td><td>6</td><td>7</td><td>7</td><td>8</td><td>9</td></tr><tr><th>Postorbital teeth</th><td>7</td><td>5</td><td>6</td><td>5</td><td>6</td><td>6</td><td>5</td></tr><tr><th>Rostral formula</th><td>14/2</td><td>12/2</td><td>12/2</td><td>12/2</td><td>13/1</td><td>14/2</td><td>14/2</td></tr><tr><th>Length of large 2nd chelate leg</th><td>32.0</td><td>25.5</td><td>26.5</td><td>27.4</td><td>-</td><td>-</td><td>-</td></tr><tr><th>Length of small 2nd chelate leg</th><td>24.5</td><td>21.0</td><td>21.0</td><td>21.4</td><td>-</td><td>14.0</td><td>-</td></tr><tr><th>Uropod length</th><td>7.0</td><td>7.0</td><td>6.0</td><td>7.0</td><td>7.0</td><td>4.5</td><td>-</td></tr><tr><th>Telson length</th><td>5.0</td><td>5.0</td><td>5.0</td><td>5.0</td><td>6.0</td><td>3.5</td><td>-</td></tr><tr><th>Weight</th><td>1.28</td><td>0.93</td><td>0.75</td><td>1.18</td><td>1.09</td><td>0.29</td><td>0.26</td></tr><tr><th>Sex</th><td>♂</td><td>♀</td><td>♂</td><td>♂</td><td>♂</td><td>♀</td><td>♂</td></tr></tbody></table>
Table 4 in The atyid shrimp (Crustacea: Decapoda: Atyidae) rostrum: phylogeny versus adaptation, taxonomy versus trophic ecology
<p>Table 4. Swallowing time efficiency (in seconds) for two specimens of <i>Proteus</i>, while feeding on <i>Troglocaris</i> without rostra and with long undamaged rostra.</p><table><tbody><tr><th>Time efficiency: mean ± SD (<i>n</i>)</th></tr></tbody><tbody><tr><th></th><td>Shrimps with long undamaged rostra</td><td>Shrimps without rostra</td></tr><tr><th><i>Proteus</i> 1</th><td>38.5 ± 12.8 (<i>n</i> = 6)</td><td>14.3 ± 12.6 (<i>n</i> = 6)</td></tr><tr><th><i>Proteus</i> 2</th><td>10.3 ± 8.5 (<i>n</i> = 4)</td><td>9.3 ± 6.8 (<i>n</i> = 7)</td></tr><tr><th>Mean ± SD, mean ± standard deviation; <i>n</i>, number of eaten shrimps.</th></tr></tbody></table>
TABLE 2 in Cambarus (P.) theepiensis, a new species of crayfish (Decapoda: Cambaridae) from the coalfields region of Eastern Kentucky and Southwestern West Virginia, USA
<p><b>TABLE 2.</b> Pleopodal egg diameters and instar condition for <i>Cambarus theepiensis,</i> <b>n. sp.</b> ED denotes average egg diameter in mm; asterisk denotes incomplete complement of eggs or instars.</p><table><tbody><tr><th>Stream</th><th>Date</th><th>Female TCL</th><th>Condition of eggs/instars</th></tr></tbody><tbody><tr><th>Hood Cr, Lawrence Co. KY</th><td>29 Apr 2012</td><td>30.7</td><td>141 attached eggs; ED = 2.5</td></tr><tr><th>Hood Cr, Lawrence Co. KY</th><td>29 Apr 2012</td><td>38.5</td><td>157 attached eggs; ED = 2.6</td></tr><tr><th>Type locality</th><td>4 Jun 2012</td><td>42.3</td><td>210 attached eggs; ED = 2.8</td></tr><tr><th>Type locality</th><td>4 Jun 2012</td><td>39.1</td><td>174 attached eggs; ED = 2.7</td></tr><tr><th>Type locality</th><td>4 Jun 2012</td><td>41.1</td><td>209 attached eggs; ED = 2.5</td></tr><tr><th>Type locality</th><td>3 Jul 2012</td><td>41.3</td><td>43 attached eggs*; ED = 2.7</td></tr><tr><th>Type locality</th><td>3 Jul 2012</td><td>38.6</td><td>2nd stage instars</td></tr><tr><th>Type locality</th><td>3 Jul 2012</td><td>38.3</td><td>2nd stage instars</td></tr><tr><th>Type locality</th><td>3 Jul 2012</td><td>39.4</td><td>3rd stage instars</td></tr><tr><th>Type locality</th><td>3 Sep 2012</td><td>46.4</td><td>4th stage instars</td></tr><tr><th>Type locality</th><td>10 Oct 2012</td><td>49.1</td><td>4th stage instars</td></tr></tbody></table>
TABLE 1 in Cambarus (P.) theepiensis, a new species of crayfish (Decapoda: Cambaridae) from the coalfields region of Eastern Kentucky and Southwestern West Virginia, USA
<p><b>TABLE 1.</b> Measurements (mm) of <i>Cambarus theepiensis</i>, new species.</p><table><tbody><tr><th></th><th>Holotype</th><th>Allotype</th><th>Morphotype</th></tr></tbody><tbody><tr><th>Carapace Total carapace length Postorbital length</th><td>46.6 38.9</td><td>42.6 35.7</td><td>47.3 39.6</td></tr><tr><th>Length cephalic section Width Depth Length rostrum</th><td>29.1 25.0 19.0 9.8</td><td>26.4 23.2 17.6 7.6</td><td>29.0 25.6 19.9 8.0</td></tr><tr><th>Length acumen Length areola Width areola</th><td>3.3 16.5 3.0</td><td>3.0 15.4 4.3</td><td>7.7 22.7 4.0</td></tr><tr><th>Antennal scale Width</th><td>3.1</td><td>2.7</td><td>3.2</td></tr><tr><th>Abdomen Width</th><td>20.5</td><td>20.5</td><td>21.5</td></tr><tr><th>Cheliped Length mesial margin palm Width palm Depth palm Length dactyl Length carpus Width carpus</th><td>13.3 21.1 11.2 30.3 13.5 11.0</td><td>9.4 15.3 9.1 21.2 10.3 9.1</td><td>12.5 19.4 11.1 27.0 12.7 11.4</td></tr><tr><th>Length dorsal margin merus Depth merus</th><td>20.0 11.8</td><td>16.2 9.4</td><td>18.1 9.4</td></tr><tr><th>Gonopod length</th><td>9.5</td><td>N.A.</td><td>9.9</td></tr></tbody></table>
Table 3 in The atyid shrimp (Crustacea: Decapoda: Atyidae) rostrum: phylogeny versus adaptation, taxonomy versus trophic ecology
<p>Table 3. Analyses of sexual differences and differences due to the presence of <i>Proteus</i> in adult specimens of three major <i>Troglocaris</i> s. str. phylogroups (W-Slo; E-Slo; Adriatic) and in pooled phylogroups (Soča and Istra phylogroups added).</p><table><tbody><tr><th>Phylogroup/MC</th><th></th><th>Sexual dimorphism (males/females)</th><th></th><th>Presence of <i>Proteus</i> (presence/absence)</th></tr></tbody><tbody><tr><th></th><td><i>Proteus</i> YES</td><td><i>Proteus</i> NO</td><td></td><td>Males</td><td></td><td>Females</td></tr><tr><th></th><td><i>Z</i></td><td>Sig.</td><td><i>Z</i></td><td>Sig.</td><td><i>Z</i></td><td>Sig.</td><td><i>Z</i></td><td>Sig.</td></tr><tr><th><b>All phylogroups</b></th></tr><tr><th>CL</th><td>4.297</td><td><b>0.000</b> 83/161</td><td>2.688</td><td><b>0.000</b> 67/88</td><td>1.521</td><td><b>0.020</b> 83/67</td><td>2.552</td><td><b>0.000</b> 161/88</td></tr><tr><th>CT</th><td>2.389</td><td><b>0.000</b> 83/161</td><td>1.434</td><td><b>0.033</b> 67/88</td><td>2.454</td><td><b>0.000</b> 83/67</td><td>3.075</td><td><b>0.000</b> 161/88</td></tr><tr><th>RO</th><td>1.659</td><td><b>0.008</b> 74/151</td><td>1.581</td><td><b>0.014</b> 59/78</td><td>3.497</td><td><b>0.000</b> 74/59</td><td>4.074</td><td><b>0.000</b> 151/78</td></tr><tr><th><i>ROT1</i></th><td>0.720</td><td>0.678 74/149</td><td>0.895</td><td>0.399 59/79</td><td>3.190</td><td><b>0.000</b> 74/59</td><td>3.568</td><td><b>0.000</b> 149/79</td></tr><tr><th><i>ROT2</i></th><td>1.460</td><td><b>0.028</b> 83/159</td><td>1.117</td><td>0.165 65/88</td><td>2.370</td><td><b>0.000</b> 83/65</td><td>3.258</td><td><b>0.000</b> 159/88</td></tr><tr><th><i>ROT3</i></th><td>0.662</td><td>0.774 74/151</td><td>0.752</td><td>0.625 60/79</td><td>2.839</td><td><b>0.000</b> 74/60</td><td>3.293</td><td><b>0.000</b> 151/79</td></tr><tr><th>rcl</th><td>0.835</td><td>0.488 74/151</td><td>0.900</td><td>0.392 59/78</td><td>4.101</td><td><b>0.000</b> 74/59</td><td>4.202</td><td><b>0.000</b> 151/78</td></tr><tr><th>ctcl</th><td>1.070</td><td>0.202 83/161</td><td>1.364</td><td><b>0.048</b> 67/88</td><td>2.454</td><td><b>0.000</b> 83/67</td><td>3.231</td><td><b>0.000</b> 161/88</td></tr><tr><th>r12rct</th><td>1.548</td><td><b>0.017</b> 74/149</td><td>1.787</td><td><b>0.003</b> 59/78</td><td>1.478</td><td><b>0.025</b> 74/59</td><td>1.614</td><td><b>0.011</b> 149/78</td></tr><tr><th>r3r</th><td>1.731</td><td><b>0.005</b> 74/149</td><td>0.929</td><td>0.353 59/78</td><td>1.151</td><td>0.141 74/59</td><td>0.600</td><td>0.865 149/78</td></tr><tr><th><b>(1) W-Slo</b></th></tr><tr><th>CL</th><td>3.115</td><td><b>0.000</b> 34/70</td><td>1.648</td><td><b>0.009</b> 21/26</td><td>1.938</td><td><b>0.001</b> 34/21</td><td>1.742</td><td><b>0.005</b> 70/26</td></tr><tr><th>CT</th><td>1.873</td><td><b>0.002</b> 34/70</td><td>0.868</td><td>0.439 21/26</td><td>2.230</td><td><b>0.000</b> 34/21</td><td>2.703</td><td><b>0.000</b> 70/26</td></tr><tr><th>RO</th><td>0.642</td><td>0.805 31/63</td><td>1.346</td><td>0.053 19/21</td><td>3.321</td><td><b>0.000</b> 31/19</td><td>3.591</td><td><b>0.000</b> 63/21</td></tr><tr><th><i>ROT1</i></th><td>1.141</td><td>0.148 31/61</td><td>0.744</td><td>0.637 19/21</td><td>2.337</td><td><b>0.000</b> 31/19</td><td>2.188</td><td><b>0.000</b> 61/21</td></tr><tr><th><i>ROT2</i></th><td>1.190</td><td>0.118 34/68</td><td>0.868</td><td>0.439 21/26</td><td>2.362</td><td><b>0.000</b> 34/21</td><td>2.605</td><td><b>0.000</b> 68/26</td></tr><tr><th><i>ROT3</i></th><td>1.356</td><td>0.051 31/63</td><td>0.412</td><td>0.996 19/21</td><td>2.546</td><td><b>0.000</b> 31/19</td><td>2.268</td><td><b>0.000</b> 63/21</td></tr><tr><th>rcl</th><td>1.636</td><td><b>0.009</b> 31/63</td><td>0.910</td><td>0.379 19/21</td><td>3.211</td><td><b>0.000</b> 31/19</td><td>3.780</td><td><b>0.000</b> 63/21</td></tr><tr><th>ctcl</th><td>1.242</td><td>0.091 34/70</td><td>0.868</td><td>0.439 21/26</td><td>2.230</td><td><b>0.000</b> 34/21</td><td>2.703</td><td><b>0.000</b> 70/26</td></tr><tr><th>r12rct</th><td>1.868</td><td><b>0.002</b> 31/61</td><td>1.393</td><td><b>0.041</b> 19/21</td><td>3.030</td><td><b>0.000</b> 31/19</td><td>3.116</td><td><b>0.000</b> 61/21</td></tr><tr><th>r3r</th><td>1.793</td><td><b>0.003</b> 31/61</td><td>0.863</td><td>0.446 19/21</td><td>0.711</td><td>0.693 31/19</td><td>0.386</td><td>0.998 61/21</td></tr><tr><th></th><td><i>Proteus</i> YES</td><td><i>Proteus</i> NO</td><td></td><td>Males</td><td></td><td>Females</td></tr><tr><th></th><td><i>Z</i></td><td>Sig.</td><td><i>Z</i></td><td>Sig.</td><td><i>Z</i></td><td>Sig.</td><td><i>Z</i></td><td>Sig.</td></tr><tr><th><b>(2) E-Slo</b></th></tr><tr><th>CL</th><td>2.611</td><td><b>0.000</b> 22/44</td><td>1.783</td><td><b>0.003</b> 31/37</td><td>0.684</td><td>0.738 22/31</td><td>1.239</td><td>0.093 44/37</td></tr><tr><th>CT</th><td>1.219</td><td>0.103 22/44</td><td>0.970</td><td>0.303 31/37</td><td>1.099</td><td>0.178 22/31</td><td>1.991</td><td><b>0.001</b> 44/37</td></tr><tr><th>RO</th><td>1.718</td><td><b>0.005</b> 20/42</td><td>0.951</td><td>0.326 27/34</td><td>1.632</td><td><b>0.010</b> 20/27</td><td>2.768</td><td><b>0.000</b> 42/34</td></tr><tr><th><i>ROT1</i></th><td>0.473</td><td>0.979 20/42</td><td>0.289</td><td>1.000 27/35</td><td>2.341</td><td><b>0.000</b> 22/31</td><td>2.913</td><td><b>0.000</b> 42/35</td></tr><tr><th><i>ROT2</i></th><td>1.480</td><td><b>0.025</b> 22/44</td><td>0.543</td><td>0.930 30/37</td><td>1.641</td><td><b>0.009</b> 22/30</td><td>2.635</td><td><b>0.000</b> 44/37</td></tr><tr><th><i>ROT3</i></th><td>0.421</td><td>0.994 20/42</td><td>0.648</td><td>0.795 28/35</td><td>1.854</td><td><b>0.002</b> 20/28</td><td>2.434</td><td><b>0.000</b> 42/35</td></tr><tr><th>rcl</th><td>1.104</td><td>0.174 20/42</td><td>0.520</td><td>0.950 27/34</td><td>2.210</td><td><b>0.000</b> 20/27</td><td>3.382</td><td><b>0.000</b> 42/34</td></tr><tr><th>ctcl</th><td>0.783</td><td>0.571 22/44</td><td>0.859</td><td>0.451 31/37</td><td>1.010</td><td>0.260 22/31</td><td>2.074</td><td><b>0.000</b> 44/37</td></tr><tr><th>r12rct</th><td>2.033</td><td><b>0.001</b> 20/42</td><td>0.778</td><td>0.581 27/34</td><td>1.255</td><td>0.086 20/27</td><td>0.789</td><td>0.562 42/34</td></tr><tr><th>r3r</th><td>0.885</td><td>0.414 20/42</td><td>0.807</td><td>0.533 27/34</td><td>1.124</td><td>0.160 20/27</td><td>0.698</td><td>0.714 42/34</td></tr><tr><th><b>(3) Adriatic</b></th></tr><tr><th>CL</th><td>2.349</td><td><b>0.000</b> 17/36</td><td>1.997</td><td><b>0.001</b> 10/23</td><td>1.712</td><td><b>0.006</b> 17/10</td><td>1.344</td><td>0.054 36/23</td></tr><tr><th>CT</th><td>1.122</td><td>0.161 17/36</td><td>1.113</td><td>0.168 10/23</td><td>1.816</td><td><b>0.003</b> 17/10</td><td>0.814</td><td>0.521 36/23</td></tr><tr><th>RO</th><td>1.083</td><td>0.192 13/35</td><td>1.873</td><td><b>0.002</b> 9/21</td><td>1.439</td><td><b>0.032</b> 13/9</td><td>0.759</td><td>0.612 35/21</td></tr><tr><th><i>ROT1</i></th><td>0.535</td><td>0.937 13/35</td><td>0.478</td><td>0.976 9/21</td><td>0.808</td><td>0.531 13/9</td><td>0.794</td><td>0.555 35/21</td></tr><tr><th><i>ROT2</i></th><td>0.933</td><td>0.349 17/36</td><td>0.976</td><td>0.297 10/23</td><td>1.816</td><td><b>0.003</b> 17/10</td><td>1.430</td><td><b>0.034</b> 36/23</td></tr><tr><th><i>ROT3</i></th><td>0.670</td><td>0.761 13/35</td><td>0.837</td><td>0.486 9/21</td><td>0.414</td><td>0.995 13/9</td><td>0.552</td><td>0.921 35/21</td></tr><tr><th>rcl</th><td>0.548</td><td>0.925 13/35</td><td>1.355</td><td>0.051 9/21</td><td>1.261</td><td>0.083 13/9</td><td>0.897</td><td>0.397 35/21</td></tr><tr><th>ctcl</th><td>0.911</td><td>0.378 17/36</td><td>0.999</td><td>0.271 10/23</td><td>1.712</td><td><b>0.006</b> 17/10</td><td>0.710</td><td>0.694 36/23</td></tr><tr><th>r12rct</th><td>0.839</td><td>0.482 13/35</td><td>1.633</td><td><b>0.010</b> 9/21</td><td>1.360</td><td><b>0.049</b> 13/9</td><td>1.518</td><td><b>0.020</b> 35/21</td></tr><tr><th>r3r</th><td>0.697</td><td>0.716 13/35</td><td>0.757</td><td>0.615 9/21</td><td>0.926</td><td>0.357 13/9</td><td>0.966</td><td>0.308 35/21</td></tr></tbody></table><p>(<i>Continued</i>)</p><p>Six untransformed characters and four ratios are tested by a non-parametric Two Independent Samples Kolmogorov–Smirnov test (two-tailed). MC, morphological character; <i>Z</i>, Kolmogorov–Smirnov <i>Z</i> value; for each MC and condition, numbers of specimens in compared groups are added (in superscript; for sexual dimorphism, number of males/females; for presence of <i>Proteus</i>, number of specimens co-occurring with/or living without <i>Proteus</i>); bold type indicates statistically significant differences at <i>p</i> <0.05 (under Sig.); italic type indicates numerical counted characters. Characters’ abbreviations are given in Table 2.</p>
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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.