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TABLE 1 in Revised status of Omolicna subgenus Agoo (Hemiptera: Auchenorrhyncha: Fulgoroidea: Derbidae) with a new species from Costa Rica and new country records
<p><b>TABLE 1.</b> Cenchreini used for molecular extractions.</p><table><tbody><tr><th><b>Species</b></th><th><b>Source</b></th><th><b>Collection Date</b></th><th><b>Locality</b></th></tr></tbody><tbody><tr><th><i>Agoo xavieri</i></th><td>FLREC</td><td>12-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Anchimothon dubia</i></th><td>FLREC</td><td>14-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Omolicna brunnea</i></th><td>FLREC</td><td>12-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Omolicna dominicana</i></th><td>University of Delaware</td><td>20-June-2004</td><td>Dominica</td></tr><tr><th><i>Omolicna fulva</i></th><td>University of Delaware</td><td>August-2005</td><td>U.S.A., DE</td></tr><tr><th><i>Omolicna joi</i></th><td>FLREC</td><td>29-July-2018</td><td>U.S.A., FL</td></tr><tr><th><i>Omolicna latens</i></th><td>FLREC</td><td>22-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Omolicna proxima</i></th><td>FDACS-DPI</td><td>18-July-1971</td><td>Trinidad</td></tr><tr><th><i>Omolicna puertana</i></th><td>University of Puerto Rico</td><td>23-March-2019</td><td>U.S.A., PR</td></tr><tr><th><i>Omolicna nero</i></th><td>University of Delaware</td><td>5-July-2003</td><td>Belize</td></tr><tr><th><i>Omolicna triata</i></th><td>FLREC</td><td>12-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Cenchrea dorsalis</i></th><td>University of Delaware</td><td>29-August-1991</td><td>St. Vincent</td></tr><tr><th><i>Neocenchrea heidemanni</i></th><td>University of Delaware</td><td>2-September-2009</td><td>U.S.A., DE</td></tr></tbody></table>
TABLE 2 in Revised status of Omolicna subgenus Agoo (Hemiptera: Auchenorrhyncha: Fulgoroidea: Derbidae) with a new species from Costa Rica and new country records
<p><b>TABLE 2.</b> GenBank accession numbers for included Cenchreini.</p><table><tbody><tr><th><b>Species</b></th><th><b>Source</b></th><th><b>Collection Date</b></th><th><b>Locality</b></th></tr></tbody><tbody><tr><th><i>Agoo xavieri</i></th><td>FLREC</td><td>12-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Anchimothon dubia</i></th><td>FLREC</td><td>14-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Omolicna brunnea</i></th><td>FLREC</td><td>12-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Omolicna dominicana</i></th><td>University of Delaware</td><td>20-June-2004</td><td>Dominica</td></tr><tr><th><i>Omolicna fulva</i></th><td>University of Delaware</td><td>August-2005</td><td>U.S.A., DE</td></tr><tr><th><i>Omolicna joi</i></th><td>FLREC</td><td>29-July-2018</td><td>U.S.A., FL</td></tr><tr><th><i>Omolicna latens</i></th><td>FLREC</td><td>22-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Omolicna proxima</i></th><td>FDACS-DPI</td><td>18-July-1971</td><td>Trinidad</td></tr><tr><th><i>Omolicna puertana</i></th><td>University of Puerto Rico</td><td>23-March-2019</td><td>U.S.A., PR</td></tr><tr><th><i>Omolicna nero</i></th><td>University of Delaware</td><td>5-July-2003</td><td>Belize</td></tr><tr><th><i>Omolicna triata</i></th><td>FLREC</td><td>12-May-2018</td><td>Costa Rica</td></tr><tr><th><i>Cenchrea dorsalis</i></th><td>University of Delaware</td><td>29-August-1991</td><td>St. Vincent</td></tr><tr><th><i>Neocenchrea heidemanni</i></th><td>University of Delaware</td><td>2-September-2009</td><td>U.S.A., DE</td></tr></tbody></table>
Table 4 in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)
<p><b>Table 4</b> Shell characters of <i>Lepidodesma aligera</i> and Lepidodesma languilati</p><table><tbody><tr><th>Characters</th><th><i>Lepidodesma aligera</i> (<i>n</i> =3)</th><th><i>Lepidodesma languilati</i> (<i>n</i> =6)</th></tr></tbody><tbody><tr><th>Length (mm)</th><td>161.38–175.22</td><td>192.25–207.67</td></tr><tr><th>Height (mm)</th><td>98.67–108.56</td><td>121.46–138.34</td></tr><tr><th>Width (mm)</th><td>75.33–81.78</td><td>83.18–88.35</td></tr><tr><th>Shell shape</th><td>Subtriangular</td><td>Subtriangular</td></tr><tr><th>Pseudocardinal teeth</th><td>Nearly absent</td><td>Nearly absent</td></tr><tr><th>Lateral teeth</th><td>2L, 1R</td><td>2L, 1R</td></tr><tr><th>Umbo position</th><td>1/4 of shell length; umbo higher than the dorsal margin</td><td>1/3 of shell length; umbo obviously higher than the dorsal margin</td></tr><tr><th>Umbo sculpture</th><td>Doubly looped or doubly noduled ridges</td><td>Doubly looped ridges</td></tr><tr><th>Umbo pocket</th><td>Deep, wide</td><td>Deep, wide</td></tr><tr><th>Surface sculpture</th><td>Ridges that follow the growth lines, two strong posterior dorsal ridges, and scattered nodules on the post-dorsal wing</td><td>Ridges that follow the growth lines and two strong posterior dorsal ridges</td></tr><tr><th>Nacre color</th><td>Orange, umbo pocket is pale green</td><td>Orange, umbo pocket is lilac</td></tr><tr><th>Dorsal margin</th><td>Anterior margin oval, dorsal margin nearly perpendicular</td><td>Anterior margin oval, with the dorsal margin curved</td></tr><tr><th></th><td>to the posterior margin, strongly curved upwards near the downwards posterior edge</td></tr><tr><th>Ventral margin</th><td>Slightly curve</td><td>Slightly curve</td></tr></tbody></table><p><i>L</i> left valve, <i>R</i> right valve</p>
TABLE 4. Pairwise comparison for the 18 S in Revised status of Omolicna subgenus Agoo (Hemiptera: Auchenorrhyncha: Fulgoroidea: Derbidae) with a new species from Costa Rica and new country records
<p><b>TABLE 4.</b> Pairwise comparison for the 18S gene based on 1,000 bootstrap replications using the p-distance method.</p><table><tbody><tr><th></th><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><th>11</th></tr></tbody><tbody><tr><th>1</th><td><i>Agoo dahliana</i></td><td></td><td>0.003</td><td>0.008</td><td>0.008</td><td>0.008</td><td>0.007</td><td>0.008</td><td>0.008</td><td>0.008</td><td>0.007</td><td>0.007</td></tr><tr><th>2</th><td><i>Agoo xavieri</i></td><td>0.012</td><td></td><td>0.008</td><td>0.008</td><td>0.008</td><td>0.007</td><td>0.007</td><td>0.008</td><td>0.008</td><td>0.007</td><td>0.007</td></tr><tr><th>3</th><td><i>Omolicna latens</i></td><td>0.097</td><td>0.098</td><td></td><td>0.003</td><td>0.003</td><td>0.008</td><td>0.008</td><td>0.003</td><td>0.003</td><td>0.008</td><td>0.008</td></tr><tr><th>4</th><td><i>Omolicna brunnea</i></td><td>0.096</td><td>0.097</td><td>0.009</td><td></td><td>0.002</td><td>0.008</td><td>0.008</td><td>0.001</td><td>0.002</td><td>0.008</td><td>0.008</td></tr><tr><th>5</th><td><i>Omolicna puertana</i></td><td>0.099</td><td>0.100</td><td>0.011</td><td>0.006</td><td></td><td>0.008</td><td>0.008</td><td>0.002</td><td>0.003</td><td>0.008</td><td>0.008</td></tr><tr><th>6</th><td><i>Anchimothon dubia</i></td><td>0.075</td><td>0.076</td><td>0.103</td><td>0.103</td><td>0.102</td><td></td><td>0.004</td><td>0.008</td><td>0.009</td><td>0.006</td><td>0.005</td></tr><tr><th>7</th><td><i>Omolicna nero</i></td><td>0.079</td><td>0.075</td><td>0.100</td><td>0.103</td><td>0.100</td><td>0.023</td><td></td><td>0.008</td><td>0.009</td><td>0.006</td><td>0.006</td></tr><tr><th>8</th><td><i>Omolicna triata</i></td><td>0.098</td><td>0.099</td><td>0.009</td><td>0.002</td><td>0.006</td><td>0.103</td><td>0.103</td><td></td><td>0.002</td><td>0.008</td><td>0.008</td></tr><tr><th>9</th><td><i>Omolicna joi</i></td><td>0.098</td><td>0.099</td><td>0.009</td><td>0.006</td><td>0.009</td><td>0.105</td><td>0.104</td><td>0.008</td><td></td><td>0.008</td><td>0.008</td></tr><tr><th>10</th><td><i>Neocenchrea heidemanni</i></td><td>0.067</td><td>0.068</td><td>0.100</td><td>0.100</td><td>0.098</td><td>0.041</td><td>0.047</td><td>0.100</td><td>0.102</td><td></td><td>0.001</td></tr><tr><th>11</th><td><i>Cenchrea dorsalis</i></td><td>0.065</td><td>0.067</td><td>0.099</td><td>0.098</td><td>0.096</td><td>0.040</td><td>0.045</td><td>0.099</td><td>0.100</td><td>0.053</td><td></td></tr></tbody></table>
Table 2 F in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)
<p><b>Table 2</b> F-type mtDNA sequences used for molecular analyses and corresponding GenBank numbers</p><table><tbody><tr><th><b>Family</b></th><th><b>Subfamily</b></th><th><b>Tribe</b></th><th><b>Taxa</b></th><th><b>Accession number</b></th></tr></tbody><tbody><tr><th>Unionidae</th><td>Unioninae</td><td>Nodulariini</td><td><i>Cuneopsis demangei</i></td><td>NC_066664</td><td>MZ571513</td></tr><tr><td><i>Cuneopsis heudei</i></td><td>NC_042471</td><td>MH919389</td></tr><tr><td><i>Cuneopsis celtiformis</i></td><td>MZ571520</td><td></td></tr><tr><td><i>Cuneopsis rufescens</i></td><td>NC_066663</td><td>MZ571512</td></tr><tr><td><i>Schistodesmus</i> sp. ‘ <i>Lamprotula gottschei</i> ’</td><td>NC_023806</td><td>KJ018924</td></tr><tr><td><i>Schistodesmus spinosus</i></td><td>NC_066662</td><td>MZ571511</td></tr><tr><td><i>Schistodesmus lampreyanus</i></td><td>NC_042470</td><td>MH919388</td></tr><tr><td><i>Tchangsinaia piscicula</i></td><td>NC_026306</td><td>KP273584</td></tr><tr><td><i>Nodularia breviconcha</i></td><td>MT955592</td><td></td></tr><tr><td><i>Nodularia douglasiae</i></td><td>NC_026111</td><td>KM657954</td></tr><tr><td><i>Pseudocuneopsis capitata</i></td><td>NC_042469</td><td>MH919387</td></tr><tr><td><i>Pseudocuneopsis sichuanensis</i></td><td>NC_066661</td><td>MZ571510</td></tr><tr><td>Unionini</td><td><i>Unio delphinus</i></td><td>NC_033854</td><td>KT326917</td></tr><tr><td><i>Unio pictorum</i></td><td>NC_015310</td><td>HM014130</td></tr><tr><td><i>Unio crassus</i></td><td>NC_033976</td><td>KY290446</td></tr><tr><td><i>Unio tumidus</i></td><td>KY021076</td><td></td></tr><tr><td><i>Unio elongatulus</i></td><td>MN594537</td><td></td></tr><tr><td><i>Unio mancus</i></td><td>MN594538</td><td></td></tr><tr><td>Aculamprotulini</td><td><i>Aculamprotula polysticta</i></td><td>MK728823</td><td></td></tr><tr><td><i>Aculamprotula scripta</i></td><td>NC_045529</td><td>KF991456</td></tr><tr><td><i>Aculamprotula coreana</i></td><td>NC_026035</td><td>JX050180</td></tr><tr><td><i>Aculamprotula tientsinensis</i></td><td>NC_029210</td><td></td></tr><tr><td><i>Aculamprotula tortuosa</i></td><td>NC_021404</td><td>KC109779</td></tr><tr><td>Anodontini</td><td><i>Alasmidonta varicosa</i></td><td>NC_038155</td><td>MG938673</td></tr><tr><td><i>Lasmigona complanata</i></td><td>OM736811</td><td></td></tr><tr><td><i>Platynaias compressa</i></td><td>HM856638</td><td></td></tr><tr><td><i>Prolasmidonta heterodon</i></td><td>MG905826</td><td></td></tr><tr><td><i>Utterbackia imbecillis</i></td><td>NC_015479</td><td>HM856637</td></tr><tr><td><i>Utterbackia peninsularis</i></td><td>HM856636</td><td></td></tr><tr><td><i>Pyganodon grandis</i></td><td>NC_013661</td><td>FJ809754</td></tr><tr><td><i>Anodonta anatina</i></td><td>NC_022803</td><td>KF030964</td></tr><tr><td><i>Anodonta exulcerata</i></td><td>MN594533</td><td></td></tr><tr><td><i>Anodonta nuttalliana</i></td><td>MN594534</td><td></td></tr><tr><td><i>Anodonta cygnea</i></td><td>NC_036488</td><td>MG385135</td></tr><tr><td><i>Pseudanodonta complanata</i></td><td>MN594535</td><td></td></tr><tr><td>Cristariini</td><td><i>Anemina arcaeformis</i></td><td>NC_026674</td><td>KF667530</td></tr><tr><td><i>Anemina euscaphys</i></td><td>NC_026792</td><td>KP187851</td></tr><tr><td><i>Sinanodonta tumens</i></td><td>LC592406</td><td></td></tr><tr><td><i>Sinanodonta lucida</i></td><td>NC_026673</td><td>KF667529</td></tr><tr><td><i>Sinanodonta woodiana</i></td><td>HQ283346</td><td></td></tr><tr><td><i>Beringiana fukuharai</i></td><td>LC592410</td><td></td></tr><tr><td><i>Cristaria plicata</i></td><td>KM233451</td><td></td></tr><tr><td>Lanceolariini</td><td><i>Acuticosta chinensis</i></td><td>NC_042472</td><td>MH919390</td></tr><tr><td><i>Lanceolaria lanceolata</i></td><td>NC_023955</td><td>KJ144818</td></tr><tr><td><i>Lanceolaria gladiola</i></td><td>KY067441</td><td></td></tr><tr><td><i>Lanceolaria grayii</i></td><td>NC_026686</td><td>KJ495725</td></tr><tr><td>Lepidodesmini</td><td><i>Lepidodesma aligera</i> <i>a</i></td><td>OP859025</td><td></td></tr><tr><td><i>Lepidodesma languilati</i> <i>a</i></td><td>OQ910483</td><td></td></tr><tr><th></th><td>Parreysiinae</td><td>Lamellidentini</td><td><i>Lamellidens marginalis</i></td><td>NC_062877</td><td>MT230549</td></tr><tr><th></th><td>Gonideinae</td><td>Gonideini</td><td><i>Parvasolenaia rivularis</i></td><td>NC_039839</td><td>KX966393</td></tr><tr><th></th><td><i>Ptychorhynchus pfisteri</i></td><td>KY067440</td><td></td></tr><tr><th></th><td><i>Sinosolenaia carinata</i></td><td>NC_023250</td><td>KC848654</td></tr><tr><th></th><td><i>Sinosolenaia oleivora</i></td><td>NC_022701</td><td>KF296320</td></tr><tr><th></th><td><i>Sinosolenaia iridinea</i></td><td>MT477834</td><td></td></tr><tr><th></th><td><i>Microcondylaea bonellii</i></td><td>NC_044111</td><td>MK994772</td></tr><tr><th></th><td>Lamprotulini</td><td><i>Lamprotula caveata</i></td><td>NC_030336</td><td>KX060991</td></tr><tr><th></th><td><i>Lamprotula leaii</i></td><td>NC_023346</td><td>JQ691662</td></tr><tr><th></th><td><i>Lamprotula cornuumlunae</i></td><td>MK728822</td><td></td></tr><tr><th></th><td><i>Potomida littoralis</i></td><td>NC_030073</td><td>KT247374</td></tr><tr><th></th><td><i>Pronodularia japanensis</i></td><td>AB055625</td><td></td></tr><tr><th></th><td>Pseudodontini</td><td><i>Monodontina vondembuschiana</i></td><td>NC_044112</td><td>MK994774</td></tr><tr><th></th><td><i>Pilsbryoconcha exilis</i></td><td>NC_044124</td><td>MK994776</td></tr><tr><th></th><td>Contradentini</td><td><i>Lens contradens</i></td><td>MW242812</td><td></td></tr><tr><th></th><td><i>Physunio superbus</i></td><td>MW242814</td><td></td></tr><tr><th></th><td>Rectidentini</td><td><i>Hyriopsis bialata</i></td><td>MW242816</td><td></td></tr><tr><th></th><td><i>Rectidens sumatrensis</i></td><td>MW242818</td><td></td></tr><tr><th></th><td>Chamberlainiini</td><td><i>Sinohyriopsis cumingii</i></td><td>NC_011763</td><td>FJ529186</td></tr><tr><th></th><td><i>Sinohyriopsis schlegelii</i></td><td>NC_015110</td><td>HQ641406</td></tr><tr><th></th><td><i>Chamberlainia hainesiana</i></td><td>NC_044110</td><td>MK994770</td></tr><tr><th></th><td>Ambleminae</td><td>Lampsilini</td><td><i>Lampsilis powellii</i></td><td>NC_037720</td><td>MF326971</td></tr><tr><th></th><td><i>Lampsilis siliquoidea</i></td><td>NC_037721</td><td>MF326973</td></tr><tr><th></th><td><i>Venustaconcha ellipsiformis</i></td><td>FJ809753</td><td></td></tr><tr><th></th><td><i>Lampsilis cardium</i></td><td>BK010478</td><td></td></tr><tr><th></th><td><i>Lampsilis cariosa</i></td><td>OM736866</td><td></td></tr><tr><th></th><td><i>Lampsilis ornata</i></td><td>NC_005335</td><td>AY365193</td></tr><tr><th></th><td><i>Leaunio lienosus</i></td><td>BK010479</td><td></td></tr><tr><th></th><td><i>Potamilus alatus</i></td><td>KU559011</td><td></td></tr><tr><th></th><td><i>Potamilus streckersoni</i></td><td>ON855351</td><td></td></tr><tr><th></th><td><i>Potamilus leptodon</i></td><td>NC_028522</td><td>KT723012</td></tr><tr><th></th><td><i>Toxolasma parvum</i></td><td>NC_015483</td><td>HM856639</td></tr><tr><th></th><td>Popenaiadini</td><td><i>Popenaias popeii</i></td><td>NC_050058</td><td>MT648776</td></tr><tr><th></th><td>Amblemini</td><td><i>Amblema plicata</i></td><td>NC_050056</td><td>MT648774</td></tr><tr><th></th><td>Pleurobemini</td><td><i>Elliptio complanata</i></td><td>BK010477</td><td></td></tr><tr><th></th><td><i>Pleurobema oviforme</i></td><td>NC_050057</td><td>MT648775</td></tr><tr><th></th><td>Quadrulini</td><td><i>Quadrula quadrula</i></td><td>NC_013658</td><td>FJ809750</td></tr><tr><th></th><td><i>Uniomerus tetralasmus</i></td><td>BK010480</td><td></td></tr><tr><th>Margaritiferidae</th><td>Margaritiferinae</td><td><i>Margaritifera dahurica</i></td><td>NC_023942</td><td>KF514426</td></tr><tr><td><i>Margaritifera falcata</i></td><td>NC_015476</td><td>HM856634</td></tr><tr><td><i>Margaritifera margaritifera</i></td><td>KY996745</td><td></td></tr><tr><td><i>Pseudunio marocanus</i></td><td>NC_034911</td><td>KY131953</td></tr><tr><td><i>Cumberlandia monodonta</i></td><td>NC_034846</td><td>KU873123</td></tr><tr><td>Gibbosulinae</td><td><i>Gibbosula crassa</i></td><td>NC_037942</td><td>MH319826</td></tr><tr><td></td><td><i>Gibbosula rochechouartii</i></td><td>KX378172</td><td></td></tr><tr><th>Hyriidae</th><td>Hyriinae</td><td><i>Echyridella menziesii</i></td><td>NC_034845</td><td>KU873121</td></tr><tr><th>Iridinidae</th><td>Iridininae</td><td><i>Mutela dubia</i></td><td>NC_034844</td><td>KU873120</td></tr><tr><th>Mycetopodidae</th><td>Anodontitinae</td><td><i>Anodontites trapesialis</i></td><td>KU873119</td><td></td></tr><tr><th>Trigoniidae</th><td><i>Neotrigonia margaritacea</i></td><td>NC_034843</td><td>KU873118</td></tr></tbody></table><p><sup>aThe</sup> sequence from this study</p>
TABLE 1 in A molecular phylogeny of Garuleum (Calenduleae, Asteraceae) in southern Africa
<p><b>TABLE 1.</b> List of species and Genbank accessions in the phylogenetic analysis.</p><table><tbody><tr><th></th><th></th><th></th><th></th><th><b>Genbank accession numbers</b></th></tr><tr><th></th><th><b>Collector</b></th><th><b>Coll. No.</b></th><th><b>Herbarium</b></th><th><b>trnL-trnF spacer</b></th><th><b>ITS</b></th></tr><tr><th><b>OUTGROUP SAMPLES</b></th></tr></tbody><tbody><tr><th><i>Dimorphotheca pluvialis</i> (L.) Moench</th><td>Cultivated, ACCID: 86,120</td><td>ACCID: 86,120 (DIM3-1)</td><td>IAMFPC</td><td>KM356195.1</td><td>KM356171.1</td></tr><tr><th><i>Osteospermum asperulum</i> (DC.) Norl.</th><td>A. Wood</td><td>435</td><td>S</td><td>FJ861567</td><td>FJ861477</td></tr><tr><th><i>Printzia auriculata</i> Harv.</th><td>N.G. Bergh</td><td>NGB2199</td><td>-</td><td>KR559440</td><td>KR559458.1</td></tr><tr><th><i>Artemisia chinensis</i> Burm. ex DC.</th><td>M.H. Chung</td><td>Chung 1076</td><td>UC</td><td>JX073822.1</td><td>JX051756.1</td></tr><tr><th><b>GARULEUM SAMPLES</b></th></tr><tr><th><i>G. album</i> S.Moore</th><td>P.B. Phillipson</td><td>4326</td><td>GRA</td><td>-</td><td>OR924282</td></tr><tr><th><i>G. bipinnatum</i> 1 (Thunb.) Less.</th><td>J. van Zyl</td><td>11</td><td>BLFU</td><td>OR918440</td><td>OR924283</td></tr><tr><th><i>G. bipinnatum</i> 2 (Thunb.) Less.</th><td>J. van Zyl</td><td>16</td><td>BLFU</td><td>OR918441</td><td>OR924284</td></tr><tr><th><i>G. bipinnatum</i> 3 (Thunb.) Less.</th><td>D. Shearing</td><td>K207</td><td>GRA</td><td>OR918442</td><td>-</td></tr><tr><th><i>G. latifolium</i> Harv.</th><td>J. Huse</td><td>191</td><td>NH</td><td>OR918443</td><td>OR924286</td></tr><tr><th><i>G. pinnatifidum</i> 1 (L’Hèrit.) DC.</th><td>E. van Zinderen-Bakker</td><td>179</td><td>BLFU</td><td>OR918444</td><td>MN251015</td></tr><tr><th><i>G. pinnatifidum</i> 2 (L’Hèrit.) DC.</th><td>R. Rossouw</td><td>61</td><td>BLFU</td><td>-</td><td>OR924287</td></tr><tr><th><i>G. pinnatifidum</i> 3 (L’Hèrit.) DC.</th><td>D.B. Muller</td><td>285</td><td>NBG</td><td>OP490276</td><td>MN251016</td></tr><tr><th><i>G. pinnatifidum</i> 4 (L’Hèrit.) DC.</th><td>H.J.T. Venter</td><td>9897</td><td>BLFU</td><td>OR918445</td><td>OR924288</td></tr><tr><th><i>G. schinzii</i> subsp. <i>schinzii</i> O.Hoffm.</th><td>M. Wilman</td><td>5369</td><td>GRA</td><td>OR918446</td><td>OR924289</td></tr><tr><th><i>G. schinzii</i> subsp. <i>crinitum</i> (Dinter) Merxm.</th><td>C. Mannheimer</td><td>2882</td><td>GRA</td><td>OR918447</td><td>OR917752</td></tr><tr><th><i>G. sonchifolium</i> (DC.) Norl.</th><td>F.B. Wright</td><td>-</td><td>NH</td><td>OR918448</td><td>OR924290</td></tr><tr><th><i>G. tanacetifolium</i> 1 (MacOwan) Norl.</th><td>J. van Zyl</td><td>21</td><td>BLFU</td><td>OR918449</td><td>OR924292</td></tr><tr><th><i>G. tanacetifolium</i> 2 (MacOwan) Norl.</th><td>J. van Zyl</td><td>17</td><td>BLFU</td><td>OR918450</td><td>OR924291</td></tr><tr><th><i>G. tanacetifolium</i> 3 (MacOwan) Norl.</th><td>J. van Zyl</td><td>22</td><td>BLFU</td><td>OR918451</td><td>OR924293</td></tr><tr><th><i>G. woodii</i> Schinz.</th><td>M.L Jacobsz</td><td>s.n.</td><td>-</td><td>OR918452</td><td>OR924294</td></tr></tbody></table>
TABLE 3 in Revised status of Omolicna subgenus Agoo (Hemiptera: Auchenorrhyncha: Fulgoroidea: Derbidae) with a new species from Costa Rica and new country records
<p><b>TABLE 3.</b> Pairwise comparison for the COI gene based on 1,000 bootstrap replications using the <i>p</i> -distance method.</p><table><tbody><tr><th></th><th></th><th>1</th><th>2</th><th>3</th><th>4</th><th>5</th><th>6</th><th></th><th>7</th><th>8</th><th>9</th><th>10</th><th>11</th><th>12</th><th>13</th></tr></tbody><tbody><tr><th>1</th><td><i>Agoo dahliana</i></td><td></td><td>0.014</td><td>0.016</td><td>0.016</td><td>0.016</td><td>0.016</td><td><i>Agoo dahliana</i></td><td>0.015</td><td>0.016</td><td>0.016</td><td>0.015</td><td>0.016</td><td>0.015</td><td>0.017</td></tr><tr><th>2</th><td><i>Agoo xavieri</i></td><td>0.147</td><td></td><td>0.015</td><td>0.015</td><td>0.015</td><td>0.016</td><td><i>Agoo xavieri</i></td><td>0.016</td><td>0.016</td><td>0.017</td><td>0.015</td><td>0.016</td><td>0.014</td><td>0.016</td></tr><tr><th>3</th><td><i>Omolicna puertana</i></td><td>0.187</td><td>0.207</td><td></td><td>0.014</td><td>0.013</td><td>0.014</td><td><i>Omolicna puertana</i></td><td>0.014</td><td>0.014</td><td>0.015</td><td>0.013</td><td>0.014</td><td>0.015</td><td>0.015</td></tr><tr><th>4</th><td><i>Omolicna triata</i></td><td>0.197</td><td>0.205</td><td>0.145</td><td></td><td>0.013</td><td>0.015</td><td><i>Omolicna triata</i></td><td>0.014</td><td>0.015</td><td>0.014</td><td>0.013</td><td>0.014</td><td>0.015</td><td>0.015</td></tr><tr><th>5</th><td><i>Omolicna brunnea</i></td><td>0.204</td><td>0.216</td><td>0.137</td><td>0.132</td><td></td><td>0.014</td><td><i>Omolicna brunnea</i></td><td>0.015</td><td>0.016</td><td>0.015</td><td>0.014</td><td>0.014</td><td>0.016</td><td>0.015</td></tr><tr><th>6</th><td><i>Omolicna dominicana</i></td><td>0.216</td><td>0.210</td><td>0.147</td><td>0.157</td><td>0.152</td><td></td><td><i>Omolicna dominicana</i></td><td>0.015</td><td>0.014</td><td>0.015</td><td>0.015</td><td>0.014</td><td>0.015</td><td>0.016</td></tr><tr><th>7</th><td><i>Anchimothon dubia</i></td><td>0.184</td><td>0.197</td><td>0.149</td><td>0.144</td><td>0.165</td><td>0.165</td><td><i>Anchimothon dubia</i></td><td></td><td>0.015</td><td>0.016</td><td>0.015</td><td>0.015</td><td>0.015</td><td>0.015</td></tr><tr><th>8</th><td><i>Omolicna nero</i></td><td>0.223</td><td>0.226</td><td>0.160</td><td>0.163</td><td>0.187</td><td>0.152</td><td><i>Omolicna nero</i></td><td>0.171</td><td></td><td>0.015</td><td>0.014</td><td>0.015</td><td>0.016</td><td>0.016</td></tr><tr><th>9</th><td><i>Omolicna joi</i></td><td>0.221</td><td>0.246</td><td>0.165</td><td>0.157</td><td>0.166</td><td>0.165</td><td><i>Omolicna joi</i></td><td>0.187</td><td>0.174</td><td></td><td>0.014</td><td>0.015</td><td>0.017</td><td>0.016</td></tr><tr><th>10</th><td><i>Omolicna uhleri</i></td><td>0.189</td><td>0.192</td><td>0.131</td><td>0.132</td><td>0.157</td><td>0.149</td><td><i>Omolicna uhleri</i></td><td>0.163</td><td>0.152</td><td>0.152</td><td></td><td>0.014</td><td>0.016</td><td>0.016</td></tr><tr><th>11</th><td><i>Omolicna latens</i></td><td>0.204</td><td>0.233</td><td>0.158</td><td>0.137</td><td>0.150</td><td>0.160</td><td><i>Omolicna latens</i></td><td>0.158</td><td>0.184</td><td>0.178</td><td>0.139</td><td></td><td>0.016</td><td>0.016</td></tr><tr><th>12</th><td><i>Neocenchrea heidemanni</i></td><td>0.160</td><td>0.155</td><td>0.189</td><td>0.176</td><td>0.199</td><td>0.187</td><td><i>Neocenchrea heidemanni</i></td><td>0.160</td><td>0.192</td><td>0.218</td><td>0.176</td><td>0.204</td><td></td><td>0.016</td></tr><tr><th>13</th><td><i>Cedusa _inflata</i></td><td>0.223</td><td>0.212</td><td>0.192</td><td>0.191</td><td>0.191</td><td>0.215</td><td><i>Cedusa _inflata</i></td><td>0.189</td><td>0.221</td><td>0.226</td><td>0.204</td><td>0.210</td><td>0.192</td><td></td></tr></tbody></table>
TABLE 1 in Two new species of eriophyid mites (Acari: Eriophyidae) from Malaysia
<p><b>TABLE 1. Morphological comparison of female species of <i>Neodicrothrix grandcaputus</i> sp. nov. to</b> <i>N. piperae</i>, N. <i>tiliacorae</i>, <i>N. celloshieldae</i> and <i>N. rutacevagrans</i>. <b>(L</b>, <b>length; W</b>, <b>width; N</b>, <b>number; D</b>, <b>distance; -, not applicable)</b></p><table><tbody><tr><th>Characters</th><th>N. grandcaputus <b>sp. nov.</b></th><th>N. piperae</th><th>N. tiliacorae</th><th>N. celloshieldae</th><th><i>N. rutacevagrans</i></th></tr></tbody><tbody><tr><th>Body L</th><td>140–163</td><td>130–140</td><td>190</td><td>140</td><td>140–150</td></tr><tr><th>Body W</th><td>48–68</td><td>58–60</td><td>80</td><td>45</td><td>45</td></tr><tr><th>Prodorsal shield L</th><td>66–80</td><td>60</td><td>70</td><td>60</td><td>85</td></tr><tr><th>D between scapular ubercles</th><td>26–30</td><td>10</td><td>30</td><td>15</td><td>25</td></tr><tr><th>Scapular setae L</th><td>18–24</td><td>3</td><td>15</td><td>short</td><td>-</td></tr><tr><th>Setae <i>c2</i> L</th><td>6–7</td><td>10</td><td>6</td><td>-</td><td>-</td></tr><tr><th>Setae <i>f</i> L</th><td>6–8</td><td>10</td><td>8</td><td>-</td><td>-</td></tr><tr><th>Genital coverflap L</th><td>13 (10–14)</td><td>12</td><td>15</td><td>15</td><td>15</td></tr><tr><th>Genital coverflap W</th><td>20 (16–21)</td><td>18</td><td>20</td><td>18</td><td>20</td></tr><tr><th>Setae <i>3a</i> L</th><td>6 (5–7)</td><td>5</td><td>6</td><td>4</td><td>8</td></tr><tr><th>N of dorsal annuli</th><td>17–21</td><td>25</td><td>25</td><td>26</td><td>28</td></tr><tr><th>N of ventral annuli</th><td>24–16</td><td>45</td><td>25</td><td>-</td><td>-</td></tr></tbody></table>
Supplementary tables
Open the record for dataset details and reuse information.
TABLE 1 in Coleophora meridiogallica Baldizzone, Huemer & Nel, sp. n. from France (Lepidoptera, Coleophoridae)
<p><b>TABLE 1.</b> DNA barcode divergence (in %). NN = nearest neighbor.</p><table><tbody><tr><th></th><th><i>C. meridionella</i></th><th><i>C. meridiogallica</i></th></tr></tbody><tbody><tr><th>n</th><td>2</td><td>3</td></tr><tr><th>BIN</th><td>BOLD:ACT2725</td><td>BOLD:AAJ0733</td></tr><tr><th>average distance</th><td>0.16%</td><td>0.1%</td></tr><tr><th>maximum distance</th><td>0.16%</td><td>0.16%</td></tr><tr><th>distance to NN</th><td>3.51%</td><td>3.51%</td></tr></tbody></table>
Table 4. Molecular dating and ancestral area reconstruction results for Liphistius using S in Molecular phylogeny, biogeography, and species delimitation of segmented spider genus Liphistius (Araneae: Liphistiidae) in Thailand
<p><b>Table 4.</b> Molecular dating and ancestral area reconstruction results for <i>Liphistius</i> using S-DIVALIKE+J. The letters A–I correspond to geographical locations shown in Figure 4. The notation shows the biogeographic event in the phylogenetic tree (Fig. 4A) includes →: from the parent node to descendent nodes; ^: Sympatric speciation; |: Vicariance.</p><table><tbody><tr><th><b>Diversification events</b></th><th><b>Dates</b></th><th><b>DIVALIKE+J</b></th><th></th><th></th></tr><tr><th></th><th><b>(Mya)</b></th><th><b>Ancestral areas</b></th><th><b>Process</b></th><th><b>Route and probability</b></th></tr></tbody><tbody><tr><th>The most recent common ancestor of Liphistiidae</th><td>100</td><td>BCI 13.60</td><td>Dispersal:0</td><td>BCI→I|BC</td></tr><tr><th>(Fig. 4, number 1)</th><td></td><td>CEI 13.33</td><td>Vicariance:1</td><td>prob:.02</td></tr><tr><th></th><td></td><td>BEI 10.96</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Heptathelinae</th><td>58.43</td><td>I 100</td><td>Dispersal:0</td><td>I→I^I→I| I</td></tr><tr><th></th><td></td><td></td><td>Vicariance:0</td><td>prob: 1.00</td></tr><tr><th></th><td></td><td></td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of <i>Liphistius</i></th><td>53.61</td><td>BC 14.34</td><td>Dispersal:0</td><td>BC→C|B</td></tr><tr><th>(Fig. 4, number 2)</th><td></td><td>CE 14.05</td><td>Vicariance:1</td><td>prob:.03</td></tr><tr><th></th><td></td><td>C 12.37</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of <i>L. indra</i> + <i>L.</i></th><td>45.51</td><td>C 45.23</td><td>Dispersal:1</td><td>C→CE→C|E</td></tr><tr><th><i>lahu</i> (Fig. 4, number 3)</th><td></td><td>E 38.20</td><td>Vicariance:1</td><td>prob:.45</td></tr><tr><th></th><td></td><td>CE 16.50</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of <i>trang</i> species</th><td>49.61</td><td>B 39.38</td><td>Dispersal:1</td><td>B→DB→D|B</td></tr><tr><th>group + <i>bristowei</i> species group (Fig. 3, number 4)</th><td></td><td>D 30.43</td><td>Vicariance:1</td><td>prob:.30</td></tr><tr><th></th><td></td><td>BD 14.72</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of <i>bristowei</i> spe-</th><td>32.86</td><td>D 75.76</td><td>Dispersal:0</td><td>D→D^D→D|D</td></tr><tr><th>cies group (Fig. 4, number 5)</th><td></td><td>C 21.28</td><td>Vicariance:0</td><td>prob:.55</td></tr><tr><th></th><td></td><td>A 2.02</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of <i>trang</i> species</th><td>46.54</td><td>B 99.88</td><td>Dispersal:0</td><td>B→B^B→B| B</td></tr><tr><th>group (Fig. 4, number 6)</th><td></td><td>A 0.08</td><td>Vicariance:0</td><td>prob: 1.00</td></tr><tr><th></th><td></td><td>H 0.01</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Sibumasu I</th><td>41.39</td><td>B 100</td><td>Dispersal:0</td><td>B→B^B→B|B</td></tr><tr><th>clade (Fig. 4, number 7)</th><td></td><td></td><td>Vicariance:0</td><td>prob: 1.00</td></tr><tr><th></th><td></td><td></td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Sinbumasu II–</th><td>42.48</td><td>B 99.76</td><td>Dispersal:0</td><td>B→B^B→B|B</td></tr><tr><th>IV and Indochina clades (Fig. 4, number 8)</th><td></td><td>A 0.18</td><td>Vicariance:0</td><td>prob:.96</td></tr><tr><th></th><td></td><td>G 0.03</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Shibumasu II</th><td>30.56</td><td>B 99.91</td><td>Dispersal:0</td><td>B→B^B→B|B</td></tr><tr><th>(Fig. 4, number 9)</th><td></td><td>A 0.09</td><td>Vicariance:0</td><td>prob:.97</td></tr><tr><th></th><td></td><td></td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Shibumasu</th><td>38.89</td><td>B 96.03</td><td>Dispersal:1</td><td>B→AB→A|B</td></tr><tr><th>III–IV and Indochina clade (Fig. 4, number 10)</th><td></td><td>A 2.65</td><td>Vicariance:1</td><td>prob:.48</td></tr><tr><th></th><td></td><td>G 0.67</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Shibumasu III</th><td>31.69</td><td>A 51.95</td><td>Dispersal:0</td><td>A→A^A→A| A</td></tr><tr><th>(Fig. 4, number 11)</th><td></td><td>B 48.05</td><td>Vicariance:0</td><td>prob:.26</td></tr><tr><th></th><td></td><td></td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Shibumasu</th><td>34.81</td><td>B 96.15</td><td>Dispersal:1</td><td>B→BG→B| G</td></tr><tr><th>IV + Indochina clade (Fig. 4, number 12)</th><td></td><td>G 1.94</td><td>Vicariance:1</td><td>prob:.48</td></tr><tr><th></th><td></td><td>H 1.90</td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Shibumasu IV</th><td>17.02</td><td>B 100</td><td>Dispersal:0</td><td>B→B^B→B|B</td></tr><tr><th>(Fig. 4, number 13)</th><td></td><td></td><td>Vicariance:0</td><td>prob: 1.00</td></tr><tr><th></th><td></td><td></td><td>Extinction:0</td><td></td></tr><tr><th>The most recent common ancestor of Indochina</th><td>31.15</td><td>G 50.43</td><td>Dispersal:1</td><td>G→GH→G|H</td></tr><tr><th>clade (Fig. 4, number 14)</th><td></td><td>H 49.38</td><td>Vicariance:1</td><td>prob:.50</td></tr><tr><th></th><td></td><td>D 0.20</td><td>Extinction:0</td><td></td></tr></tbody></table>
Table 3 in Molecular phylogeny, biogeography, and species delimitation of segmented spider genus Liphistius (Araneae: Liphistiidae) in Thailand
<p><b>Table 3.</b> Results of Bayes factor delimitation (BFD). Marginal likelihoods of six competing species hypotheses, computed from the concatenated alignments. The log marginal likelihoods are ranked from lowest (6) to highest (1); the Bayes factor (BF) is calculated using 2lnBF = 2 × (marginal likelihood of the highest rank species model − marginal likelihood of each lower rank species model), with 2lnBF> 10 being considered as decisive support for the highest rank species model 1.</p><table><tbody><tr><th></th><th><b>Number of species</b></th><th><b>Marginal likelihood</b></th><th><b>Rank</b></th><th><b>(lnBF)</b></th><th><b>2lnBF</b></th></tr></tbody><tbody><tr><th>mGMYC</th><td>72</td><td>−31519.92277</td><td>6</td><td>52.067437</td><td>104.13487</td></tr><tr><th>bPTP</th><td>65</td><td>−31518.39951</td><td>5</td><td>50.544171</td><td>101.08834</td></tr><tr><th>mPTP</th><td>52</td><td>−31497.18524</td><td>4</td><td>29.329904</td><td>58.659809</td></tr><tr><th>sPTP</th><td>65</td><td>−31483.86739</td><td>3</td><td>16.012054</td><td>32.024108</td></tr><tr><th>sGMYC</th><td>53</td><td>−31480.86681</td><td>2</td><td>13.011473</td><td>26.022947</td></tr><tr><th>STACEY</th><td>56</td><td>−31467.85533</td><td>1</td><td></td><td></td></tr></tbody></table>
Table 1 in Molecular phylogeny, biogeography, and species delimitation of segmented spider genus Liphistius (Araneae: Liphistiidae) in Thailand
<p><b>Table 1.</b> Collecting localities with GPS coordinates, species and species group identification, and geological classification.</p><table><tbody><tr><th><b>No.</b></th><th><b>Localities</b></th><th><b>Latitude</b></th><th><b>Longitude</b></th><th><b>Altitude (m)</b></th><th><b>Sample identify</b></th><th><b>Geological terrains</b></th><th><b>Areas</b></th></tr></tbody><tbody><tr><th></th><td></td><td></td><td></td><td></td><td><i>birmanicus group:</i></td><td></td><td></td></tr><tr><th>1</th><td>Mae Sun, Fang District, Chiang Mai</td><td>19.86°N</td><td>99.05°E</td><td>1646</td><td><i>Liphistius lahu</i></td><td>Sibumasu</td><td>C</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td><b><i>bristowei</i> group:</b></td><td></td><td></td></tr><tr><th>2</th><td>Kuet Chang, Mae Taeng District, Chiang 19.32°N Mai</td><td>98.60°E</td><td>1545</td><td><i>Liphistius lannaianus</i></td><td>Sibumasu</td><td>C</td></tr><tr><th>3</th><td>Suthep, Mueang Chiang Mai District, Chiang Mai</td><td>18.80°N</td><td>98.90°E</td><td>1110</td><td><i>Liphistius bristowei s.l.</i></td><td>Sibumasu</td><td>C</td></tr><tr><th>4</th><td>Tha Pha, Mae Chaem District, Chiang Mai</td><td>18.51°N</td><td>98.48°E</td><td>1428</td><td><i>Liphistius bristowei s.l., Liphistius yamasakii</i></td><td>Sibumasu</td><td>C</td></tr><tr><th>5</th><td>Mae Koeng, Wang Chin District, Phrae</td><td>17.97°N</td><td>99.59°E</td><td>389</td><td><i>Liphistius</i> sp. WKS</td><td>Sibumasu</td><td>F</td></tr><tr><th>6</th><td>Mae Tho, Mueang Tak District, Tak-A</td><td>16.79°N</td><td>98.92°E</td><td>881</td><td><i>Liphistius jarujini</i></td><td>Sibumasu</td><td>D</td></tr><tr><th>7</th><td>Mae Tho, Mueang Tak District, Tak-B</td><td>16.72°N</td><td>98.97°E</td><td>967</td><td><i>Liphistius marginatus</i></td><td>Sibumasu</td><td>D</td></tr><tr><th>8</th><td>Wang Nam Yen, Wang Chao District, Tak 16.64°N</td><td>99.02°E</td><td>868</td><td><i>Liphistius marginatus</i></td><td>Sibumasu</td><td>D</td></tr><tr><th>9</th><td>Pang Ta Wai, Pang Sila Thong District, Kamphaeng Phet</td><td>16.09°N</td><td>99.12°E</td><td>1250</td><td><i>Liphistius maewongensis</i></td><td>Sibumasu</td><td>D</td></tr><tr><th>10</th><td>Rabam, Lan Sak District, Uthai Thani</td><td>15.61°N</td><td>99.32°E</td><td>214</td><td><i>Liphistius</i> sp. HKK</td><td>Sibumasu</td><td>D</td></tr><tr><th>11</th><td>Nong Lu, Sangkhlaburi District, Kanchanaburi-A</td><td>15.22°N</td><td>98.37°E</td><td>197</td><td><i>Liphistius</i> sp. Sangkraburi</td><td>Sibumasu</td><td>A</td></tr><tr><th>12</th><td>Nong Lu, Sangkhlaburi District, Kanchanaburi-B</td><td>15.16°N</td><td>98.34°E</td><td>183</td><td><i>Liphistius</i> sp. Sangkraburi</td><td>Sibumasu</td><td>A</td></tr><tr><th>13</th><td>Pilok, Thong Pha Phum District, Kanchanaburi</td><td>14.69°N</td><td>98.40°E</td><td>938</td><td><i>Liphistius</i> sp. TPP</td><td>Sibumasu</td><td>A</td></tr><tr><th>14</th><td>Pa Kar Ri, Dawei, Myanmar</td><td>14.10°N</td><td>98.30°E</td><td>39</td><td><i>Liphistius</i> sp. DW</td><td>Sibumasu</td><td>A</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td><b><i>trang</i> group:</b></td><td></td><td></td></tr><tr><th>15</th><td>Noen Phoem, Nakhon Thai District, Phitsanulok</td><td>17.00°N</td><td>101.01°E</td><td>1238</td><td><i>Liphistius onoi</i></td><td>Indochina</td><td>H</td></tr><tr><th>16</th><td>Sap Sawang, Nam Nao District, Phetchabun</td><td>16.74°N</td><td>101.58°E</td><td>859</td><td><i>Liphistius pusohm</i></td><td>Indochina</td><td>H</td></tr><tr><th>17</th><td>Tat Ton, Mueang Chaiyaphum, Chaiyaphum</td><td>15.98°N</td><td>102.04°E</td><td>285</td><td><i>Liphistius</i> sp. TT</td><td>Indochina</td><td>H</td></tr><tr><th>18</th><td>Huai Yang, Mueang Sakon Nakhon District, Sakon Nakhon</td><td>17.10°N</td><td>103.97°E</td><td>308</td><td><i>Liphistius isan</i></td><td>Indochina</td><td>H</td></tr><tr><th>19</th><td>Nong Pla Lai, Mueang Saraburi District, Saraburi</td><td>14.44°N</td><td>100.96°E</td><td>98</td><td><i>Liphistius</i> sp. SL</td><td>Indochina</td><td>G</td></tr><tr><th>20</th><td>Wang Phae, Kaeng Khoi District, Saraburi</td><td>14.53°N</td><td>101.04°E</td><td>74</td><td><i>Liphistius</i> sp. CPP</td><td>Indochina</td><td>H</td></tr><tr><th>21</th><td>Mittraphap, Muak Lek District, Saraburi</td><td>14.58°N</td><td>101.15°E</td><td>280</td><td><i>Liphistius tham</i></td><td>Indochina</td><td>H</td></tr><tr><th>22</th><td>Chet Khot, Kaeng Khoi District, Saraburi 14.47°N</td><td>101.17°E</td><td>201</td><td><i>Liphistius</i> sp. CK</td><td>Indochina</td><td>H</td></tr><tr><th>23</th><td>Sarika, Mueang Nakhon Nayok District, Nakhon Nayok</td><td>14.34°N</td><td>101.30°E</td><td>157</td><td><i>Liphistius</i> sp. WTK</td><td>Indochina</td><td>H</td></tr><tr><th>24</th><td>Mu Si, Mueang Nakhon Nayok District, Nakhon Nayok</td><td>14.44°N</td><td>101.37°E</td><td>754</td><td><i>Liphistius thoranie</i></td><td>Indochina</td><td>H</td></tr><tr><th>25</th><td>Na Hin Lat, Pak Phli District, Nakhon Nayok</td><td>14.37°N</td><td>101.41°E</td><td>1171</td><td><i>Liphistius thoranie</i></td><td>Indochina</td><td>H</td></tr><tr><th>26</th><td>Udom Sap, Wang Nam Khiao District, Nakhon Ratchasima</td><td>14.51°N</td><td>101.93°E</td><td>372</td><td><i>Liphistius</i> sp. SKR</td><td>Indochina</td><td>H</td></tr><tr><th>27</th><td>Na Chaluai, Na Chaluai District, Ubon Ratchathani</td><td>14.44°N</td><td>105.27°E</td><td>354</td><td><i>Liphistius dangrek</i></td><td>Indochina</td><td>H</td></tr><tr><th>28</th><td>Bang Phra, Si Racha District, Chon Buri</td><td>13.24°N</td><td>101.05°E</td><td>326</td><td><i>Liphistius sayam</i></td><td>Indochina</td><td>D</td></tr><tr><th>29</th><td>Pluang, Khao Khitchakut District, Chanthaburi</td><td>12.84°N</td><td>102.12°E</td><td>79</td><td><i>Liphistius ornatus</i></td><td>Indochina</td><td>G</td></tr><tr><th>30</th><td>Phe, Mueang Rayong District, Rayong</td><td>12.57°N</td><td>101.45°E</td><td>69</td><td><i>Liphistius phileion</i></td><td>Indochina</td><td>D</td></tr><tr><th>31</th><td>Phliu, Laem Sing District, Chanthaburi</td><td>12.53°N</td><td>102.18°E</td><td>116</td><td><i>Liphistius tenuis</i></td><td>Indochina</td><td>G</td></tr><tr><th>32</th><td>Ko Chang, Ko Chang District, Trat</td><td>12.11°N</td><td>102.27°E</td><td>84</td><td><i>Liphistius nesioticus</i></td><td>Indochina</td><td>G</td></tr><tr><th>33</th><td>Tha Kradan, Si Sawat District, Kanchanaburi-A</td><td>14.37°N</td><td>99.14°E</td><td>272</td><td><i>Liphistius erawan s.l.</i></td><td>Sibumasu</td><td>A</td></tr><tr><th>34</th><td>Tha Kradan, Si Sawat District, Kanchanaburi-B</td><td>14.39°N</td><td>99.13°E</td><td>229</td><td><i>Liphistius erawan s.l.</i></td><td>Sibumasu</td><td>A</td></tr><tr><th>35</th><td>Tha Sao,Sai Yok District, Kanchanaburi-A 14.38°N</td><td>98.93°E</td><td>380</td><td><i>Liphistius erawan s.l.</i></td><td>Sibumasu</td><td>A</td></tr><tr><th>36</th><td>Tha Sao, Sai Yok District, Kanchanaburi-B</td><td>14.24°N</td><td>99.06°E</td><td>158</td><td><i>Liphistius erawan s.l.</i></td><td>Sibumasu</td><td>A</td></tr><tr><th>37</th><td>Wang Krachae, Sai Yok District, Kanchanaburi</td><td>14.20°N</td><td>99.02°E</td><td>510</td><td><i>Liphistius</i> sp. TNL</td><td>Sibumasu</td><td>A</td></tr><tr><th>38</th><td>Suan Som, Thap Sakae District, Phra Chaup Khirikhan</td><td>11.57°N</td><td>99.54°E</td><td>108</td><td><i>Liphistius albipes</i></td><td>Sibumasu</td><td>A</td></tr><tr><th>39</th><td>Na Sak, Sawi District, Chumphon</td><td>10.23°N</td><td>98.95°E</td><td>48</td><td><i>Liphistius keeratikiati</i></td><td>Sibumasu</td><td>A</td></tr><tr><th>40</th><td>Na Kha, Suk Samran District, Ranong</td><td>9.46°N</td><td>98.50°E</td><td>52</td><td><i>Liphistius bicoloripes, Liphistius castaneus,</i></td><td>Sibumasu</td><td>B</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td><i>Liphistius schwendingeri s.l.</i></td><td></td><td></td></tr><tr><th>41</th><td>Krung Ching, Nopphitam District, Nakhon Si Thammarat</td><td>8.72°N</td><td>99.67°E</td><td>248</td><td><i>Liphistius niphanae</i></td><td>Sibumasu</td><td>B</td></tr><tr><th>42</th><td>Khlong Ya, Ao Luek District, Krabi</td><td>8.35°N</td><td>98.9°E</td><td>129</td><td><i>Liphistius</i> sp. KPN</td><td>Sibumasu</td><td>B</td></tr><tr><th>43</th><td>Mueang Krabi District, Krabi</td><td>8.24°N</td><td>98.92°E</td><td>307</td><td><i>Liphistius fuscus</i></td><td>Sibumasu</td><td>B</td></tr><tr><th>44</th><td>Khanaen, Thalang District, Phuket</td><td>8.03°N</td><td>98.36°E</td><td>89</td><td><i>Liphistius phuketensis</i></td><td>Sibumasu</td><td>B</td></tr><tr><th>45</th><td>Chong, Na Yong District, Trang</td><td>7.55°N</td><td>99.79°E</td><td>161</td><td><i>Liphistius trang</i></td><td>Sibumasu</td><td>B</td></tr><tr><th>46</th><td>Lam Khlaeng, Palian District, Trang</td><td>7.29°N</td><td>99.88°E</td><td>89</td><td><i>Liphistius</i> sp. T</td><td>Sibumasu</td><td>B</td></tr><tr><th>47</th><td>Lang Khao, Kantang District, Trang</td><td>7.27°N</td><td>99.38°E</td><td>37</td><td><i>Liphistius thaleri</i></td><td>Sibumasu</td><td>B</td></tr><tr><th>48</th><td>Kho Hong, Hat Yai District, Songkhla</td><td>7.04°N</td><td>100.51°E</td><td>162</td><td><i>Liphistius hatyai</i></td><td>Sibumasu</td><td>B</td></tr><tr><th>49</th><td>Chalung, Hat Yai District, Songkhla</td><td>6.95°N</td><td>100.24°E</td><td>167</td><td><i>Liphistius yangae s.l.</i></td><td>Sibumasu</td><td>B</td></tr><tr><th>50</th><td>Wang Prachan, Khuan Don District, Satun</td><td>6.71°N</td><td>100.17°E</td><td>174</td><td><i>Liphistius yangae s.l.</i></td><td>Sibumasu</td><td>B</td></tr><tr><th></th><td>Rayong, Thailand (GPS unavailable, Not show on the map)</td><td>-</td><td>-</td><td>-</td><td><i>Liphistius cf. ornatus</i></td><td>Indochina</td><td>D</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td><b><i>linang</i> group:</b></td><td></td><td></td></tr><tr><th>51</th><td>Sai Khao, Khok Pho District, Pattani</td><td>6.66°N</td><td>101.10°E</td><td>83</td><td><i>Liphistius indra</i></td><td>Sibumasu</td><td>E</td></tr></tbody></table>
Table 2 in A new theropod dinosaur from the Callovian Balabansai Formation of Kyrgyzstan
<p><b>Table 2.</b> Measurements of hindlimb elements of <i>A. kyrgyzicus</i> (in cm).</p><table><tbody><tr><th><b>Element</b></th><th><b>Number</b></th><th><b>Length</b></th><th><b>Proximal width</b></th><th><b>Proximal depth</b></th><th><b>Distal width</b></th><th><b>Distal depth</b></th><th><b>Shaft circumference</b></th></tr></tbody><tbody><tr><th>Femur right</th><td>IGB 2-33</td><td>90</td><td>15.5a</td><td>10.5</td><td>16</td><td>15.5</td><td>29</td></tr><tr><th>Femur left</th><td>IGB 2-32</td><td>88</td><td>18.5</td><td>10</td><td>15.5b</td><td>15.5</td><td></td></tr><tr><th>Tibia left</th><td>IGB 2-34</td><td>72</td><td>13</td><td>22</td><td>19.5</td><td>9.5</td><td>25</td></tr><tr><th>Tibia right</th><td>IGB 2-35</td><td>71.5</td><td>12c</td><td></td><td></td><td>7.5c</td><td></td></tr><tr><th>Mt II right</th><td>IGB 2-41</td><td>34.7</td><td>7.2</td><td>9</td><td>6.5</td><td>6</td><td></td></tr><tr><th>Mt III right</th><td>IGB 2-42</td><td>40</td><td>8.5</td><td>10.5d</td><td>7.7</td><td>6</td><td></td></tr><tr><th>Mt III left</th><td>IGB 2-43</td><td>39.8</td><td>9e</td><td>10.5e</td><td>7.5</td><td>5.5</td><td></td></tr><tr><th>Tibia right (Paratype)</th><td>IGB 2-48</td><td>60.5</td><td>7</td><td>11f</td><td>11</td><td>4.5</td><td>17</td></tr></tbody></table><p><sup>aLaterally</sup> incomplete. <sup>bDistorted</sup>. <sup>cSlightly</sup> damaged. <sup>dPosteriorly</sup> slightly incomplete. <sup>eSlightly</sup> rotated. <sup>fSomewhat</sup> eroded.</p>
Table 1 in Glaciambulata neumayeri gen. et sp. nov., a new Antarctic trachymedusa (Cnidaria: Hydrozoa), with a revision of the family Ptychogastriidae
<p><b>Table 1.</b> Main distinguishing characters of the genera belonging to the family Ptychogastriidae Mayer, 1900.</p><table><tbody><tr><th>Umbrella</th><th><i>Glaciambulata</i> gen. nov. Flat</th><th><b><i>Ptychogastria</i> Allman, 1878</b> Dome-shaped</th><th><b><i>Tesserogastria</i> Beyer, 1959</b> Dome-shaped</th></tr></tbody><tbody><tr><th><b>Manubrium</b></th><td>Eight-lobed</td><td>Eight-lobed</td><td>Four-lobed</td></tr><tr><th><b>Mesenteries</b></th><td>8</td><td>8</td><td>Absent</td></tr><tr><th><b>Tentacles</b></th><td>Filiform + adhesive; forming contiguous groups; inserted in superimposed rows on umbrella margin</td><td>Filiform + adhesive; forming contiguous groups; inserted in superimposed rows on umbrella margin</td><td>Filiform; reportedly not arranged in groups; inserted at varied levels on umbrella margin</td></tr><tr><th><b>Centripetal canals</b></th><td>Absent</td><td>Present/absent</td><td>Absent</td></tr><tr><th><b>Gonads</b></th><td>Ovoid; in pairs, on either side of the manubrial lobes</td><td>Ovoid; in pairs, on either side of the manubrial lobes</td><td>Elongated; simple; attached to the body of manubrium</td></tr><tr><th><b>Velum</b></th><td>Absent</td><td>Present</td><td>Present</td></tr><tr><th><b>Statocysts</b></th><td>16</td><td>16</td><td>8</td></tr><tr><th><b>Ability to swim</b></th><td>No</td><td>Yes</td><td>Yes</td></tr></tbody></table>
Table 1. Vertebral measurements for A in A new theropod dinosaur from the Callovian Balabansai Formation of Kyrgyzstan
<p><b>Table 1.</b> Vertebral measurements for <i>A. kyrgyzicus</i> (in mm)</p><table><tbody><tr><th><b>Element</b></th><th><b>Number</b></th><th><b>Centrum length</b></th><th><b>Anterior height</b></th><th><b>Anterior width</b></th><th><b>Mid-centrum width</b></th><th><b>Posterior height</b></th><th><b>Posterior width</b></th></tr></tbody><tbody><tr><th>Dorsal</th><td>IGB 2-10</td><td>115</td><td>122</td><td><i>c</i>. 105</td><td><i>c</i>. 55</td><td>124</td><td>105</td></tr><tr><th>Dorsal</th><td>IGB 2-11</td><td>120</td><td>124</td><td>108</td><td><i>c</i>. 64</td><td><i>c</i>. 120</td><td><i>c</i>. 107</td></tr><tr><th>Sacral 5</th><td>IGB 2-15</td><td>110</td><td><i>c</i>. 100</td><td><i>c</i>. 88</td><td><i>c</i>. 60</td><td>127</td><td>106</td></tr></tbody></table>
TABLE 5 in A new species of small-eared shrew of the genus Cryptotis (Mammalia, Eulipotyphla, Soricidae) from the northernmost Peruvian Andes
<p><b>TABLE 5.</b> Kimura’s two parameter (K2P) genetic distances among species of <i>Cryptotis</i> based on cytochrome b (A) and COI (B).</p><table><tbody><tr><th>A</th><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><th>11</th><th>12</th><th>13</th><th>14</th></tr></tbody><tbody><tr><th>1</th><td><i>C. alticola</i></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>C. peregrina</i></td><td>0.107</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>C. obscura</i></td><td>0.138</td><td>0.134</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>C. mexicana</i></td><td>0.136</td><td>0.139</td><td>0.045</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>C. mayensis</i></td><td>0.127</td><td>0.109</td><td>0.123</td><td>0.123</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>C. phillipsii</i></td><td>0.155</td><td>0.140</td><td>0.123</td><td>0.130</td><td>0.148</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>C. nelsoni</i></td><td>0.140</td><td>0.127</td><td>0.056</td><td>0.064</td><td>0.123</td><td>0.126</td><td>-</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>8</th><td><i>C. magna</i></td><td>0.161</td><td>0.159</td><td>0.134</td><td>0.141</td><td>0.156</td><td>0.084</td><td>0.138</td><td>-</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>9</th><td><i>C. goldmani</i></td><td>0.103</td><td>0.015</td><td>0.131</td><td>0.133</td><td>0.108</td><td>0.145</td><td>0.124</td><td>0.163</td><td>-</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>1</th><td><i>C. parva</i></td><td>0.136</td><td>0.131</td><td>0.164</td><td>0.158</td><td>0.150</td><td>0.192</td><td>0.144</td><td>0.194</td><td>0.128</td><td>-</td><td></td><td></td><td></td><td></td></tr><tr><th>11</th><td><i>C. niausa</i></td><td>0.131</td><td>0.128</td><td>0.144</td><td>0.144</td><td>0.132</td><td>0.139</td><td>0.129</td><td>0.136</td><td>0.136</td><td>0.138</td><td>-</td><td></td><td></td><td></td></tr><tr><th>12</th><td><i>C. montivaga</i></td><td>0.120</td><td>0.112</td><td>0.124</td><td>0.124</td><td>0.110</td><td>0.141</td><td>0.129</td><td>0.149</td><td>0.118</td><td>0.150</td><td>0.123</td><td>-</td><td></td><td></td></tr><tr><th>13</th><td><i>C. evaristoi</i></td><td>0.112</td><td>0.117</td><td>0.142</td><td>0.138</td><td>0.120</td><td>0.144</td><td>0.135</td><td>0.161</td><td>0.117</td><td>0.141</td><td>0.138</td><td>0.097</td><td>-</td><td></td></tr><tr><th>14</th><td>Outgroup</td><td>0.145</td><td>0.159</td><td>0.152</td><td>0.149</td><td>0.168</td><td>0.172</td><td>0.133</td><td>0.163</td><td>0.157</td><td>0.166</td><td>0.150</td><td>0.164</td><td>0.163</td><td>-</td></tr></tbody></table>
TABLE 6 in A new species of small-eared shrew of the genus Cryptotis (Mammalia, Eulipotyphla, Soricidae) from the northernmost Peruvian Andes
<p><b>TABLE 6.</b> Main diagnostic characters among <i>Cryptotis evaristoi</i> sp. noV. and other PeruVian and Ecuadorian congeneric species.</p><table><tbody><tr><th><i>C. montivaga</i> (Ecuador)</th><th><i>C. montivaga</i> (Peru)</th><th><i>C. niausa</i> (Ecuador)</th><th><i>C. equatoris</i> (Ecuador)</th><th><i>C. osgoodi</i> (Ecuador)</th><th><i>C. peruviensis</i> (holotype, Peru)</th><th><i>C. evaristoi</i> (neW species, Peru)</th></tr></tbody><tbody><tr><th>Size large (head and body length = 79.3 ± 6.03mm; Weight = 11.5 ± 2.1 g; condylobasal length = 19.87 ± 0.7 mm)</th><td>Size large (head and body length = 85.24 ± 8.48 mm; Weight = 14.2 ± 2.84 g; condylobasal length = 21.16 ± 0.51 mm)</td><td>Size large (head and body length = 77.9 ± 10.5 mm; Weight = 14.4 ± 1.8 g; condylobasal length = 21.21 ± 0,5 mm)</td><td>Size small (Head and body length = 65.73 ± 9.2 mm; Weight = 9.53 ± 0.72 g; condylobasal length = 20.32 ± 0.28 mm)</td><td>Size small (Head and body length = 68.71 ± 9.55 mm; Weight = 8.64 ± 2.88 g; condylobasal length = 19.67 ± 0.75 mm)</td><td>Size small (head and body length = 63 mm; Weight = 9 g; head and body length; condylobasal length = 20.6 mm)</td><td>Size large (head and body length = 85.8 ± 7 mm; Weight = 14 ± 2.6 g; condylobasal length = 22.34 ± 0.3 mm)</td></tr><tr><th>Tail Very short (30.4 ± 4</th><td>Tail Very short (30.75 ±</td><td>Tail short (35.5 ± 3.1</td><td>Tail short (31.87 ± 1.85</td><td>Tail short (29.86 ± 3.58</td><td>Tail medium (31 mm;</td><td>Tail short (33.7 ± 2.7</td></tr><tr><th>mm; 37% of Head and body length)</th><td>3.55 mm; 37% of Head and body length)</td><td>mm; 46% of Head and body length)</td><td>mm; 48.5% of Head and body length), tail hairy</td><td>mm; 43.5% of Head and body length), tail not hairy</td><td>49% of Head and body length)</td><td>mm; 40% of Head and body length)</td></tr><tr><th>Dorsal color grayish</th><td>Dorsal color grayish</td><td>Dorsal color grayish</td><td>Dorsal color blackish</td><td>Dorsal color blackish</td><td>Dorsal color blackish</td><td>Dorsal color grayish</td></tr><tr><th>Interorbital in dorsal VieW conVergent</th><td>Interorbital in dosal VieW parallel</td><td>Interorbital in dorsal VieW almost parallel</td><td>Interorbital in dorsal VieW conVergent and Wide</td><td>Interorbital in dorsal VieW sligthy parallel and less Wide</td><td>Interorbital in dorsal VieW slighty conVergent</td><td>Interorbital in dorsal VieW parallel</td></tr><tr><th>Anterior border of nasal With a spine-shaped process</th><td>Anterior border of nasal Without a spine-shaped process</td><td>Anterior border of nasal Without a spine- shaped process</td><td>Anterior border of nasal Without a spine-shaped process</td><td>Anterior border of nasal Without a spine-shaped process</td><td>Anterior border of nasal With a spine-shaped process</td><td>Anterior border of nasal Without a spine-shaped process</td></tr><tr><th>Braincase in dorsal VieW heXagonal</th><td>Braincase in dorsal VieW heXagonal</td><td>Braincase in dorsal VieW heXagonal</td><td>Braincase in dorsal VieW circular</td><td>Braincase in dorsal VieW circular</td><td>Braincase in dorsal VieW heXagonal</td><td>Braincase in dorsal VieW heXagonal</td></tr><tr><th>Fronto-occipital suture rounded</th><td>Fronto-occipital suture as a half heXagon</td><td>Fronto-occipital suture as a half heXagon</td><td>Fronto-occipital suture as a half heXagon</td><td>Fronto-occipital suture as a half heXagon</td><td>Fronto-occipital suture rounded</td><td>Fronto-occipital suture as rounded to triangular</td></tr><tr><th>Secondary cusp of upper incisors Very reduced fourth of anterior cusp</th><td>Secondary cusp of upper incisors approXimately half of anterior cusp</td><td>Secondary cusp of upper incisors Very reduced fourth of</td><td>Secondary cusp of upper incisors approXimately half of anterior cusp</td><td>Secondary cusp of upper incisors approXimately half of anterior cusp</td><td>Secondary cusp of upper incisors approXimately half of anterior cusp</td><td>Secondary cusp of upper incisors Very reduced a third of anterior cusp</td></tr><tr><th></th><td></td><td>anterior cusp</td><td></td><td></td><td></td><td></td></tr><tr><th>Four unicuSpid viSible in 83.3 (fully viSible in 58.3%, barely viSible in 25%), not viSible in 16.7%</th><td>Four unicuSpid not viSible in 66.67%; viSible in one mandible in 16.67%; viSible in both mandibleS in one 16.67%</td><td>Fourth unicuSpid viSible in 70.6%, in two SpecimenS not</td><td>Four unicuSpid not viSible in lateral view</td><td>Four unicuSpidS viSible in lateral view</td><td>Four unicuSpid not viSible in lateral view</td><td>Fourth unicuSpid viSible in both mandibleS in 60%; viSible alSo in one mandible in 20%; not viSible in 20%</td></tr><tr><th>Fourth unicuSpid Small, half or one-third to third unicuSpidS; in line with other unicuSpidS</th><td>Fourth unicuSpid very reduced, one-third to third unicuSpid; in line with other unicuSpidS</td><td>Fourth unicuSpid Small and rounded, half or leSS to third unicuSpid; in line with other unicuSpidS</td><td>Fourth unicuSpid very reduced, one-third to third unicuSpid; in line with other unicuSpidS</td><td>Fourth unicuSpid reduced, half to third unicuSpid; in line with other unicuSpidS</td><td>Fourth unicuSpid very reduced, one-third to third unicuSpid; not in line with other unicuSpidS</td><td>Fourth unicuSpid very reduced, one-third to fourth unicuSpidS; not in line with other unicuSpidS</td></tr><tr><th>Ectoloph of M3 Simple, form of "j"</th><td>Ectoloph of M3 Specialized, form of incomplete "w"</td><td>Ectoloph of M3 Specialized, form of "w"</td><td>Ectoloph of M3 Specialized, form of incomplete "w"</td><td>Ectoloph of M3 Specialized, form of incomplete "w"</td><td>Ectoloph of M3 Specialized, form of incomplete "w"</td><td>Ectoloph of M3 Simple, form of "j"</td></tr><tr><th>PoSt protocriSta PM4 in occluSal view iS bigger than the reSt of the tooth</th><td>PoSt protocriSta PM4 in occluSal view approximately the Same Size aS the reSt of the tooth</td><td>PoSt protocriSta PM4 in occluSal view approximately the Same Size aS the reSt of the tooth</td><td>PoSt protocriSta PM4 in occluSal view larger than the reSt of the tooth</td><td>PoSt protocriSta PM4 in occluSal view larger than the reSt of the tooth</td><td>PoSt protocriSta PM4 in occluSal view approximately the Same Size aS the reSt of the tooth</td><td>PoSt protocriSta PM4 in occluSal view twice or more than the reSt of the tooth</td></tr><tr><th>Premolar with protocone developed, without paraconule</th><td>Premolar with protocone developed, without paraconule</td><td>Premolar with protocone and paraconule developed</td><td>Premolar with protocone and paraconule developed</td><td>Premolar with protocone and paraconule developed</td><td>Premolar with protocone, and Small paraconule</td><td>Premolar with protocone developed, without paraconule</td></tr><tr><th>PoSterior border of lower inciSorS in variable poSition to anterior border of PM4</th><td>PoSterior border of lower inciSor reacheS the anterior border of PM4</td><td>PoSterior border of lower inciSorS doeS not reach the anterior border of PM4</td><td>PoSterior border of lower inciSor reacheS the anterior border of PM4</td><td>PoSterior border of lower inciSor reacheS the anterior border of PM4</td><td>PoSterior border of lower inciSor reacheS the anterior border of PM4</td><td>PoSterior border of lower inciSor reacheS the anterior border of PM4</td></tr><tr><th>Optic foramen completely viSible in lateral view</th><td>Optic foramen completely viSible in lateral view</td><td>Optic foramen completely viSible in lateral view</td><td>Optic foramen partially viSible in lateral view</td><td>Optic foramen partially viSible in lateral view</td><td>Optic foramen partially viSible in lateral view</td><td>Optic foramen partially viSible in lateral view</td></tr><tr><th>Coronoid proceSS variable, Short or large</th><td>Coronoid proceSS Short</td><td>Coronoid proceSS Short</td><td>Coronoid proceSS large</td><td>Coronoid proceSS large</td><td>Coronoid proceSS Short</td><td>Coronoid proceSS large</td></tr></tbody></table><p>……continued on the next page</p>
TABLE 4 in A new species of small-eared shrew of the genus Cryptotis (Mammalia, Eulipotyphla, Soricidae) from the northernmost Peruvian Andes
<p><b>TABLE 4.</b> Comparison of measurement inđices among seven species of <i>Cryptotis</i> from Peru anđ Ecuađor. See materials anđ methođs for abbreviations. Relative length of tail (TL/HB); relative breađth of interorbital area (PO/CBL); relative length of rostrum (PL/CBL); relative breađth of zygomatic plate (ZP/CBL); relative breađth of zygomatic plate (ZP/PL); relative length of unicuspiđ row (UTR/CBL); relative breađth of palate (M2B/PL); relative height of coronoiđ process (HCP/ML); relative posterior length of manđible (AC3/ML); relative extension of articular conđyle (AC3/HCP).</p><table><tbody><tr><th></th><th><i>C.osgoodi</i></th><th><i>C. equatoris</i></th><th><i>C. montivaga</i></th><th><i>C. montivaga</i></th><th><i>C. niausa</i></th><th><i>C.peruviensis</i></th><th><i>C. evaristoi</i></th></tr></tbody><tbody><tr><th></th><td>(N=7)</td><td>(N=3)</td><td>Ecuađor (N=5)</td><td>Peru (N=5)</td><td>(N=15)</td><td>(holotype)</td><td>(N=14)</td></tr><tr><th></th><td>X ±SD</td><td>Range</td><td>X ± SD</td><td>Range</td><td>X ± SD</td><td>Range</td><td>X ± SD</td><td>Range</td><td>X ± SD</td><td>Range</td><td>Type</td><td>X ±SD</td><td>Range</td></tr><tr><th>TL/HB</th><td>0.45 ± 0.11</td><td>0.32̅0.65</td><td>0.49 ± 0.07</td><td>0.44̅0.57</td><td>0.38 ± 0.01</td><td>0.37̅0.39</td><td>0.36 ± 0.03</td><td>0.34̅0.40</td><td>0.46 ± 0.07</td><td>0.34̅0.62</td><td>0.49</td><td>0.40 ± 0.04</td><td>0.32̅0.45</td></tr><tr><th>IO/CBL</th><td>0.24 ± 0.01</td><td>0.22̅0.25</td><td>0.24 ± 0.01</td><td>0.23̅0.24</td><td>0.23 ± 0.01</td><td>0.22̅0.24</td><td>0.47 ± 0.01</td><td>0.45̅0.48</td><td>0.22 ± 0.01</td><td>0.20̅0.23</td><td>0.28</td><td>0.24 ± 0.01</td><td>0.22̅0.25</td></tr><tr><th>PL/CBL</th><td>0.44 ± 0.01</td><td>0.43̅0.47</td><td>0.44 ± 0.004</td><td>0.44̅0.45</td><td>0.45 ± 0.01</td><td>0.43̅0.46</td><td>0.89 ± 0.02</td><td>0.86̅0.91</td><td>0.44 ± 0.01</td><td>0.42̅0.46</td><td>0.43</td><td>0.45 ± 0.00</td><td>0.44̅0.45</td></tr><tr><th>ZP/CBL</th><td>0.11 ± 0.01</td><td>0.11̅0.13</td><td>0.11 ± 0.004</td><td>0.11̅0.12</td><td>0.09 ± 0.01</td><td>0.08̅0.10</td><td>0.20 ± 0,0 1</td><td>0.19̅0.21</td><td>0.10 ± 0.01</td><td>0.08̅0.10</td><td>0.1</td><td>0.10 ± 0.00</td><td>0.09̅0.11</td></tr><tr><th>ZP/PL</th><td>0.26 ± 0.02</td><td>0.23̅0.29</td><td>0.26 ± 0.01</td><td>0.25̅0.27</td><td>0.21 ± 0.02</td><td>0.19̅0.22</td><td>0.22 ± 0.01</td><td>0.21̅0.23</td><td>0.22 ± 0.01</td><td>0.19̅0.24</td><td>0.24</td><td>0.23 ± 0.01</td><td>0.21̅0.24</td></tr><tr><th>UTR/CBL</th><td>0.14 ± 0.02</td><td>0.12̅0.16</td><td>0.13 ± 0.01</td><td>0.11̅0.13</td><td>0.13 ± 0.005</td><td>0.12̅0.13</td><td>0.27 ± 0.01</td><td>0.25̅0.28</td><td>0.12 ± 0.01</td><td>0.11̅0.14</td><td>0.13</td><td>0.12 ± 0.01</td><td>0.11̅0.13</td></tr><tr><th>M2B/PL</th><td>0.65 ± 0.04</td><td>0.60̅0.71</td><td>0.66 ± 0.04</td><td>0.63̅0.71</td><td>0.61 ± 0.03</td><td>0.57̅0.65</td><td>0.62 ± 0.01</td><td>0.61̅0.64</td><td>0.59 ± 0.03</td><td>0.52̅0.64</td><td>0.64</td><td>0.58 ± 0.01</td><td>0.56̅0.60</td></tr><tr><th>HCP/ML</th><td>0.62 ± 0.04</td><td>0.57̅0.69</td><td>0.66 ± 0.04</td><td>0.63̅0.70</td><td>0.62 ± 0.04</td><td>0.55̅0.66</td><td>0.66 ± 0.03</td><td>0.62̅0.68</td><td>0.60 ± 0.03</td><td>0.54̅0.64</td><td>0.62</td><td>0.62 ± 0.02</td><td>0.59̅0.65</td></tr><tr><th>AC3/ML</th><td>0.73 ± 0.07</td><td>0.65̅0.86</td><td>0.82 ± 0.05</td><td>0.77̅0.88</td><td>0.75 ± 0.09</td><td>0.64̅0.86</td><td>0.75 ± 0.03</td><td>0.71̅0.78</td><td>0.76 ± 0.04</td><td>0.71̅0.86</td><td>0.76</td><td>0.75 ± 0.03</td><td>0.72̅0.80</td></tr><tr><th>AC3/HCP</th><td>1.18 ± 0.10</td><td>1.08̅1.30</td><td>1.25 ± 0.03</td><td>1.22̅1.28</td><td>1.21 ± 0.09</td><td>1.11̅1.31</td><td>1.14 ± 0.06</td><td>1.07̅1.23</td><td>1.27 ± 0.09</td><td>1.14̅1.41</td><td>1.21</td><td>1.23 ± 0.03</td><td>1.18̅1.28</td></tr></tbody></table>
TABLE 2 in A new species of small-eared shrew of the genus Cryptotis (Mammalia, Eulipotyphla, Soricidae) from the northernmost Peruvian Andes
<p><b>TABLE 2.</b> Probability values of Student’s t-test for the comparison of measurements and weights among Peruvian and Ecuadorian <i>Cryptotis</i> species. Significant values are in bold.</p><table><tbody><tr><th></th><th><i>C. evaristoi</i></th><th><i>C. montivaga</i></th><th><i>C. montivaga</i></th><th><i>C. osgoodi</i></th><th><i>C. equatoris</i></th></tr></tbody><tbody><tr><th></th><td></td><td>Ecuador</td><td>Peru</td><td></td><td></td></tr><tr><th>Head and body length</th></tr><tr><th><i>C. montivaga</i> Ecuador</th><td>0.4691</td><td></td><td></td><td></td><td></td></tr><tr><th><i>C. montivaga</i> Peru</th><td>0.8379</td><td>0.6018</td><td></td><td></td><td></td></tr><tr><th><i>C. osgoodi</i></th><td><b>0.0004</b></td><td><b>0.0227</b></td><td><b>0.0075</b></td><td></td><td></td></tr><tr><th><i>C. equatoris</i></th><td><b>0.0009</b></td><td><b>0.0227</b></td><td><b>0.0096</b></td><td>0.6661</td><td></td></tr><tr><th><i>C. niausa</i></th><td>0.0771</td><td>0.4697</td><td>0.2545</td><td>0.0682</td><td>0.0878</td></tr><tr><th>Tail length</th></tr><tr><th><i>C. montivaga</i> Ecuador</th><td><b>0.0021</b></td><td></td><td></td><td></td><td></td></tr><tr><th><i>C. montivaga</i> Peru</th><td><b>0.0063</b></td><td>0.5805</td><td></td><td></td><td></td></tr><tr><th><i>C. osgoodi</i></th><td><b>0.0005</b></td><td>0.5344</td><td>0.2794</td><td></td><td></td></tr><tr><th><i>C. equatoris</i></th><td><b>0.0311</b></td><td>0.5925</td><td>0.9501</td><td>0.3943</td><td></td></tr><tr><th><i>C. niausa</i></th><td>0.6044</td><td><b>0.0083</b></td><td><b>0.0161</b></td><td><b>0.0012</b></td><td>0.0738</td></tr><tr><th>Condyle basal length</th></tr><tr><th><i>C. montivaga</i> Ecuador</th><td><b>3.9 E -6</b></td><td></td><td></td><td></td><td></td></tr><tr><th><i>C. montivaga</i> Peru</th><td><b>2.3 E -6</b></td><td>0.8637</td><td></td><td></td><td></td></tr><tr><th><i>C. osgoodi</i></th><td><b>2.6 E -10</b></td><td><b>0.0023</b></td><td><b>0.0018</b></td><td></td><td></td></tr><tr><th><i>C. equatoris</i></th><td><b>0. 7 E -8</b></td><td><b>0.0224</b></td><td><b>0.0345</b></td><td>0.1998</td><td></td></tr><tr><th><i>C. niausa</i></th><td><b>0.0250</b></td><td><b>0.0001</b></td><td><b>0.14 E -4</b></td><td><b>1.5 E -9</b></td><td><b>0.4 E -4</b></td></tr><tr><th>Mass</th></tr><tr><th><i>C. montivaga</i> Ecuador</th><td><b>0.0268</b></td><td></td><td></td><td></td><td></td></tr><tr><th><i>C. montivaga</i> Peru</th><td>0.4853</td><td>0.1685</td><td></td><td></td><td></td></tr><tr><th><i>C. osgoodi</i></th><td><b>0.0004</b></td><td>0.1650</td><td><b>0.0167</b></td><td></td><td></td></tr><tr><th><i>C. equatoris</i></th><td><b>0.0124</b></td><td>0.3051</td><td>0.0740</td><td>0.6228</td><td></td></tr><tr><th><i>C. niausa</i></th><td>0.7282</td><td><b>0.0016</b></td><td>0.2383</td><td>1.3 E -6</td><td>0.0004</td></tr></tbody></table>
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