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183 results for “Eulipotyphla”
Figure 5 in Multilocus phylogeny and morphological analyses illuminate overlooked diversity of Soriculus (Mammalia: Eulipotyphla: Soricidae), with descriptions of two new endemic species from the eastern Himalayas
Figure 5. Estimated divergence times of the genus Soriculus using BEAST.
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>
TABLE 3 in A new species of small-eared shrew of the genus Cryptotis (Mammalia, Eulipotyphla, Soricidae) from the northernmost Peruvian Andes
<p><b>TABLE 3.</b> Measurements (mm) of humerus among Peruvian and Ecuadorian species of <i>Cryptotis</i>. Total length (L1); proximal width (PW); distal width (DW); greater tuberosity to teres tubercle (GT); medial epicondyle to teres tubercle (MT); deltoid process to capitulum (CD); breadth of shaft (BS1).</p><table><tbody><tr><th></th><th><i>C. equatoris</i></th><th><i>C. osgoodi</i></th><th><i>C. montivaga</i> (Ecuador)</th><th><i>C. niausa</i></th><th><i>C. evaristoi</i></th></tr></tbody><tbody><tr><th></th><td>n =3</td><td>n = 4</td><td>n = 3</td><td>n = 3</td><td>n = 11</td></tr><tr><th>L1</th><td>7.44 ± 0.16</td><td>7.63 ± 0.09</td><td>8.05 ± 0.38</td><td>8.30 ± 0.17</td><td>8.84 ± 0.29</td></tr><tr><th></th><td>(7.25–7.54)</td><td>(7.52–7.73)</td><td>(7.82–8.49)</td><td>(8.17–8.49)</td><td>(8.52–9.36)</td></tr><tr><th>PW</th><td>2.31 ± 0.19</td><td>2.21 ± 0.09</td><td>2.58 ± 0.11</td><td>2.59 ± 0.09</td><td>2.57 ± 0.18</td></tr><tr><th></th><td>(2.18–2.52)</td><td>(2.13–2.32)</td><td>(2.46–2.66)</td><td>(2.49–2.65)</td><td>(2.32–2.9)</td></tr><tr><th>DW</th><td>3.20 ± 0.11</td><td>3.16 ± 0.11</td><td>3.40 ± 0,22</td><td>2.67 ± 0.58</td><td>3.51 ± 0.15</td></tr><tr><th></th><td>(3.10–3.32)</td><td>(3.01–3.26)</td><td>(3,15–3.57)</td><td>(3.48–4.48)</td><td>(3.25–3.73)</td></tr><tr><th>GT</th><td>4.22 ± 0.32</td><td>4.01 ± 0.25</td><td>4.62 ± 0.24</td><td>4.80 ± 0.24</td><td>4.71 ± 0.21</td></tr><tr><th></th><td>(3.88–4.50)</td><td>(3.81–4.36)</td><td>(4.43–4.89)</td><td>(4.53–4.98)</td><td>(4.49–5.2)</td></tr><tr><th>MT</th><td>3.38 ± 0.08</td><td>3.54 ± 0.22</td><td>3.40 ± 0.12</td><td>3.92 ± 0.44</td><td>3.64 ± 0.21</td></tr><tr><th></th><td>(3.29–3.43)</td><td>(3.20–3.67)</td><td>(3.30–3.54)</td><td>(3.50–4.38)</td><td>(3.35–4.14)</td></tr><tr><th>CD</th><td>5.62 ± 0.21</td><td>5.68 ± 0.14</td><td>5.52 ± 0.46</td><td>6.05 ± 0.18</td><td>6.20 ± 0.26</td></tr><tr><th></th><td>(5.38–5.79)</td><td>(5.53–5.86)</td><td>(5.09–6.00)</td><td>(5.84–6.15)</td><td>(5.87–6.65)</td></tr><tr><th>BS1</th><td>1.05 ± 0.05</td><td>1.10 ± 0.05</td><td>1.16 ± 0.02</td><td>1.21 ± 0.13</td><td>1.26 ± 0.04</td></tr><tr><th></th><td>(1.01–1.10)</td><td>(1.05–1.15)</td><td>(1.15–1.19)</td><td>(1.11–1.36)</td><td>(1.23–1.36)</td></tr></tbody></table>
TABLE 1 in A new species of small-eared shrew of the genus Cryptotis (Mammalia, Eulipotyphla, Soricidae) from the northernmost Peruvian Andes
<p><b>TABLE 1.</b> External anđ craniomađibular measurements (mm), anđ weights (g) from seven Peruvian anđ Ecuađorian species of the genus <i>Cryptotis</i>.</p><table><tbody><tr><th></th><th><i>C. montivaga</i></th><th></th><th><i>C. montivaga</i></th><th></th><th><i>C. niausa</i></th><th></th><th><i>C. osgoodi</i></th><th></th><th><i>C. equatoris</i></th><th><i>C. peruviensis</i></th><th><i>C. evaristoi</i></th><th></th></tr></tbody><tbody><tr><th></th><td>Ecuađor</td><td></td><td>Perủ</td><td></td><td>Ecuađor</td><td></td><td>Ecuađor</td><td></td><td>Ecuađor</td><td></td><td>Perủ</td><td>Perủ</td><td></td></tr><tr><th></th><td>X ± SD</td><td>Range</td><td>n</td><td>X ± SD</td><td>Range</td><td>n</td><td>X ± SD</td><td>Range</td><td>n</td><td>X ± SD</td><td>Range</td><td>n</td><td>X ± SD</td><td>Range</td><td>n</td><td>Type</td><td>X ± SD</td><td>Range</td><td>n</td></tr><tr><th>External measurements</th></tr><tr><th>HB</th><td>79.3 ± 6.03</td><td>65̅89</td><td>14</td><td>85.24 ± 8.48</td><td>73̅99</td><td>6</td><td>77.7 ± 10.52</td><td>54.5̅93</td><td>15</td><td>68.71 ± 9.55</td><td>54̅76</td><td>7</td><td>65.73 ± 9.20</td><td>56.2 -76</td><td>3</td><td>63.15</td><td>85.8 ± 6.96</td><td>70 ̅ 96</td><td>16</td></tr><tr><th>TL</th><td>30.4 ± 3.96</td><td>22̅38</td><td>14</td><td>30.75 ± 3.55</td><td>25̅35</td><td>6</td><td>35.5 ± 3.06</td><td>30̅40.8</td><td>14</td><td>29.86 ± 3.58</td><td>24̅35</td><td>7</td><td>31.87 ± 1.85</td><td>30̅33.7</td><td>3</td><td>30.5</td><td>33.7 ± 2.73</td><td>29 ̅ 37</td><td>16</td></tr><tr><th>HF</th><td>13.5 ± 1.33</td><td>11.8̅17</td><td>13</td><td>14.8 ± 0.76</td><td>14̅16</td><td>5</td><td>14.7 ± 1.02</td><td>13.4̅17.4</td><td>15</td><td>13.67 ± 1.15</td><td>12̅15</td><td>7</td><td>13.47 ± 1.36</td><td>12.4̅15</td><td>3</td><td>14</td><td>14.9 ± 0.47</td><td>14̅16.6</td><td>16</td></tr><tr><th>6</th><td>11.5 ± 2.10</td><td>11̅15</td><td>14</td><td>14.2 ± 2.84</td><td>12.5̅16.5</td><td>5</td><td>14.4 ± 1.79</td><td>12̅17</td><td>15</td><td>8.64 ± 2.88</td><td>6̅13</td><td>7</td><td>9.53 ± 0.72</td><td>8.7̅10</td><td>3</td><td>9</td><td>14 ± 2.55</td><td>11̅16</td><td>16</td></tr><tr><th>Cranial measurements</th></tr><tr><th>CBL</th><td>19.87 ± 0.70</td><td>18.23̅ 20.65</td><td>10</td><td>21.16 ± 0.51</td><td>20.2̅21.7</td><td>6</td><td>21.21 ±0.45</td><td>20.77̅ 21.85</td><td>5</td><td>19.67 ± 0.75</td><td>18.23̅20.65</td><td>7</td><td>20.32 ± 0.28</td><td>20.10 - 20.63</td><td>3</td><td>20.39</td><td>22.34 ± 0.27</td><td>21.9̅ 22.8</td><td>14</td></tr><tr><th>BB</th><td>9.6 4 ± 0.46</td><td>8.74̅ 10.29</td><td>10</td><td>10.57 ± 0.18</td><td>10.28̅ 10.72</td><td>6</td><td>10.38 ± 0.34</td><td>9.96̅ 10.91</td><td>5</td><td>9.54 ± 0.46</td><td>8.74̅10.14</td><td>7</td><td>9.86 ± 0.46</td><td>9.38̅ 10.29</td><td>3</td><td>10.46</td><td>10.75 ± 0.24</td><td>10.4̅ 11.2</td><td>14</td></tr><tr><th>ZP</th><td>2.27 ± 0.14</td><td>2.03̅2.48</td><td>10</td><td>2.09 ± 0.06</td><td>2̅2.17</td><td>6</td><td>2.00 ± 0.17</td><td>1.75̅2.13</td><td>5</td><td>2.26 ± 0.15</td><td>2.03̅2.48</td><td>7</td><td>2.3 ± 0.10</td><td>2.19̅2.38</td><td>3</td><td>2</td><td>2.24 ± 0.09</td><td>2.1̅2.4</td><td>14</td></tr><tr><th>PO</th><td>4.72 ± 0.24</td><td>4.27̅4.99</td><td>10</td><td>4.98 ± 0.14</td><td>4.84̅5.2</td><td>6</td><td>4.86 ± 0.15</td><td>4.63̅5.02</td><td>5</td><td>4.67 ± 0.26</td><td>4.27̅4.99</td><td>7</td><td>4.86 ± 0.14</td><td>4.70̅4.94</td><td>3</td><td>4.82</td><td>5.26 ± 0.16</td><td>5.0̅5.6</td><td>14</td></tr><tr><th>U1B</th><td>2.45 ± 0.14</td><td>2.21̅2.6</td><td>10</td><td>2.55 ± 0.09</td><td>2.47̅2.7</td><td>6</td><td>2.55 ± 0.16</td><td>2.3̅2.74</td><td>5</td><td>2.46 ± 0.13</td><td>2.33̅2.60</td><td>7</td><td>2.44 ± 0.20</td><td>2.21̅2.59</td><td>3</td><td>2.27</td><td>2.73 ± 0.07</td><td>2.6̅2.8</td><td>14</td></tr><tr><th>U3B</th><td>2.92 ± 0.26</td><td>2.6̅3.38</td><td>10</td><td>3.03 ± 0.1</td><td>2.93̅3.2</td><td>6</td><td>3.35 ± 0.21</td><td>3.13̅3.68</td><td>5</td><td>2.93 ± 0.31</td><td>2.60̅3.38</td><td>7</td><td>2.91 ± 0.17</td><td>2.81̅3.11</td><td>3</td><td>3.05</td><td>3.18 ± 0.11</td><td>2.9̅3.3</td><td>14</td></tr><tr><th>M2B</th><td>5.74 ± 0.21</td><td>5.49̅6.22</td><td>10</td><td>5.89 ± 0.16</td><td>5.78̅6.2</td><td>6</td><td>5.79 ± 0.32</td><td>5.43̅6.13</td><td>5</td><td>5.65 ± 0.12</td><td>5.49̅5.85</td><td>7</td><td>5.95 ± 0.24</td><td>5.79̅6.22</td><td>3</td><td>5.91</td><td>5.82 ± 0.11</td><td>5.6̅6.0</td><td>14</td></tr><tr><th>PL</th><td>8.81 ± 0.41</td><td>7.91̅9.32</td><td>10</td><td>9.43 ± 0.19</td><td>9.24̅9.7</td><td>6</td><td>9.56 ± 0.17</td><td>9.37̅9.79</td><td>5</td><td>8.74 ± 0.46</td><td>7.91̅9.32</td><td>7</td><td>8.98 ± 0.21</td><td>8.80̅9.21</td><td>3</td><td>8.6</td><td>9.96 ± 0.17</td><td>9.6̅10.2</td><td>14</td></tr><tr><th>TR</th><td>7.83 ± 0.28</td><td>7.32̅8.25</td><td>10</td><td>8.25 ± 0.14</td><td>8.05̅8.37</td><td>6</td><td>7.98 ± 0.40</td><td>7.49̅8.55</td><td>5</td><td>7.72 ± 0.22</td><td>7.32̅7.98</td><td>7</td><td>8.08 ± 0.25</td><td>7.79̅8.25</td><td>3</td><td>7.9</td><td>8.43 ± 0.18</td><td>8.0̅8.7</td><td>14</td></tr><tr><th>UTR</th><td>2.65 ± 0.31</td><td>2.3̅3.18</td><td>10</td><td>2.82 ± 0.12</td><td>2.69̅3.01</td><td>6</td><td>2.66 ± 0.08</td><td>2.57̅2.78</td><td>5</td><td>2.69 ± 0.35</td><td>2.34̅3.18</td><td>7</td><td>2.55 ± 0.22</td><td>2.30̅2.68</td><td>3</td><td>2.42</td><td>2.78 ± 0.13</td><td>2.5̅2.9</td><td>14</td></tr><tr><th>MTR</th><td>5.53 ± 0.25</td><td>5.14̅5.97</td><td>10</td><td>5.81 ± 0.08</td><td>5.72̅5.91</td><td>5</td><td>5.65 ± 0.37</td><td>5.11̅5.99</td><td>5</td><td>5.41 ± 0.15</td><td>5.14̅5.61</td><td>7</td><td>5.79 ± 0.26</td><td>5.49̅5.97</td><td>3</td><td>5.63</td><td>5.99 ± 0.16</td><td>5.58̅6.2</td><td>14</td></tr><tr><th>6M1</th><td>1.65 ± 0.16</td><td>1.42̅1.87</td><td>10</td><td>1.73 ± 0.1</td><td>1.63̅1.9</td><td>6</td><td>1.30 ± 0.14</td><td>1.19̅1.54</td><td>5</td><td>1.60 ± 0.14</td><td>1.42̅1.80</td><td>7</td><td>1.76 ± 0.15</td><td>1.59̅1.87</td><td>3</td><td>1.73</td><td>1.98 ± 0.09</td><td>1.8̅2.1</td><td>14</td></tr><tr><th></th><td><i>C. montivaga</i></td><td></td><td><i>C. montivaga</i></td><td></td><td><i>C. niausa</i></td><td></td><td><i>C. osgoodi</i></td><td></td><td><i>C. equatoris</i></td><td></td><td><i>C. peruviensis</i></td><td><i>C. evaristoi</i></td><td></td></tr><tr><th></th><td>Ecuađor</td><td></td><td>Perủ</td><td></td><td></td><td>Ecuađor</td><td></td><td>Ecuađor</td><td></td><td>Ecuađor</td><td></td><td>Perủ</td><td>Perủ</td><td></td></tr><tr><th></th><td>X ± SD</td><td>Range</td><td>n</td><td>X ± SD</td><td>Range</td><td>n</td><td>X ± SD Range</td><td>n</td><td>X ± SD</td><td>Range</td><td>n</td><td>X ± SD</td><td>Range</td><td>n</td><td>Type</td><td>X ± SD</td><td>Range</td><td>n</td></tr><tr><th>Manđibular measurements</th></tr><tr><th>ML</th><td>6.69 ± 0.42</td><td>5.95̅7.35</td><td>10</td><td>7.2 ± 0.27</td><td>6.92̅7.6</td><td>6</td><td>7.32 ± 0.57</td><td>6.84̅8.28</td><td>5</td><td>6.62 ± 0.48</td><td>5.95̅7.35</td><td>7</td><td>6.84 ± 0.21</td><td>6.65̅7.06</td><td>3</td><td>7.08</td><td>7.71 ± 0.20</td><td>7.6̅8.2</td><td>14</td></tr><tr><th>HCP</th><td>4.21 ± 0.24</td><td>3.89̅4.65</td><td>10</td><td>4.68 ± 0.15</td><td>4.41̅4.87</td><td>6</td><td>4.50 ± 0.16</td><td>4.22̅4.61</td><td>5</td><td>4.09 ± 0.15</td><td>3.89̅4.30</td><td>7</td><td>4.48 ± 0.16</td><td>4.33̅4.65</td><td>3</td><td>4.54</td><td>4.75 ± 0.14</td><td>4.5̅5.0</td><td>14</td></tr><tr><th>HCV</th><td>2.78 ± 0.12</td><td>2.5̅2.97</td><td>10</td><td>3.24 ± 0.16</td><td>3̅3.39</td><td>6</td><td>3.21 ± 0.38</td><td>2.88̅3.86</td><td>5</td><td>2.76 ± 0.12</td><td>2.50̅2.87</td><td>7</td><td>2.84 ± 0.13</td><td>2.71̅2.97</td><td>3</td><td>3.07</td><td>3.34 ± 0.12</td><td>3.1̅3.5</td><td>14</td></tr><tr><th>HAC</th><td>3.69 ± 0.29</td><td>3.24̅4.13</td><td>10</td><td>4.14 ± 0.17</td><td>3.95̅4.31</td><td>5</td><td>4.00 ± 0.09</td><td>3.89̅4.09</td><td>5</td><td>3.59 ± 0.26</td><td>3.24̅4.10</td><td>7</td><td>3.93 ± 0.24</td><td>3.66̅4.13</td><td>3</td><td>4.25</td><td>4.51 ± 0.22</td><td>4.1̅4.9</td><td>14</td></tr><tr><th>BAC</th><td>3.13 ± 0.22</td><td>2.68̅3.48</td><td>10</td><td>3.35 ± 0.17</td><td>3.16̅3.55</td><td>5</td><td>3.28 ± 0.20</td><td>3.04̅3.49</td><td>5</td><td>3.07 ± 0.22</td><td>2.68̅3.33</td><td>7</td><td>3.27 ± 0.20</td><td>3.09̅3.48</td><td>3</td><td>3.22</td><td>3.51 ± 0.10</td><td>3.3̅3.6</td><td>14</td></tr><tr><th>AC3</th><td>5.06 ± 0.51</td><td>4.41̅5.82</td><td>10</td><td>5.31 ± 0.11</td><td>4.22̅5.42</td><td>5</td><td>5.46 ± 0.34</td><td>5.13̅6.0</td><td>5</td><td>4.82 ± 0.40</td><td>4.41̅5.39</td><td>7</td><td>5.61 ± 0.19</td><td>5.44̅5.82</td><td>3</td><td>4.78</td><td>5.82 ± 0.20</td><td>5.5̅6.1</td><td>14</td></tr><tr><th>TRM</th><td>5.89 ± 0.23</td><td>5.56̅6.23</td><td>10</td><td>6.69 ± 0.1 6.59̅6.82</td><td>6</td><td>6.37 ± 0.21</td><td>6.11̅6.67</td><td>5</td><td>5.89 ± 0.21</td><td>5.56̅6.16</td><td>7</td><td>5.90 ± 0.32</td><td>5.59̅6.23</td><td>3</td><td>6.15</td><td>6.76 ± 0.10</td><td>6.6̅6.9</td><td>14</td></tr><tr><th>m1L</th><td>1.87 ± 0.08</td><td>1.74̅2.0</td><td>10</td><td>1.75 ± 0.09</td><td>1.66̅1.87</td><td>5</td><td>1.90 ± 0.10</td><td>1.74̅2.0</td><td>5</td><td>1.86 ± 0.09</td><td>1.74̅2.00</td><td>7</td><td>1.90 ± 0.04</td><td>1.86̅1.93</td><td>3</td><td>1.76</td><td>1.93 ± 0.07</td><td>1.8̅2.1</td><td>14</td></tr></tbody></table>
FIGURE 3. G in C-heterochromatin variation in the karyotype reflects species level distinction between Erinaceus roumanicus and E. concolor (Eulipotyphla: Erinaceidae) in Turkey
FIGURE 3. G-banded karyotype of Erinaceus concolor (female from Konya in central Anatolia).
FIGURE 2 in C-heterochromatin variation in the karyotype reflects species level distinction between Erinaceus roumanicus and E. concolor (Eulipotyphla: Erinaceidae) in Turkey
FIGURE 2. Conventional karyotype of Erinaceus roumanicus (male from Edirne in Thrace).
Data from: Post K-Pg diversification of the mammalian order Eulipotyphla as suggested by phylogenomic analyses of ultra-conserved elements
The origin of the mammalian order Eulipotyphla has been debated intensively with arguments around whether they began diversifying before or after the Cretaceous-Palaeogene (K-Pg) boundary at 66 Ma. Here, we used an in-solution nucleotide capture method and next generation DNA sequencing to determine the sequence of hundreds of ultra-conserved elements (UCEs), and conducted phylogenomic and molecular dating analyses for the four extant eulipotyphlan lineages—Erinaceidae, Solenodontidae, Soricidae, and Talpidae. Concatenated maximum-likelihood analyses with single or partitioned models and a coalescent species-tree analysis showed that divergences among the four major eulipotyphlan lineages occurred within a short period of evolutionary time, but did not resolve the interrelationships among them. Alternative suboptimal phylogenetic hypotheses received consistently the same amount of support from different UCE loci, and were not significantly different from the maximum likelihood tree topology, suggesting the prevalence of stochastic lineage sorting. Molecular dating analyses that incorporated among-lineage evolutionary rate differences supported a scenario where the four eulipotyphlan families diversified between 57.8 and 63.2 Ma. Given short branch lengths with low support values, traces of rampant genome-wide stochastic lineage sorting, and post K-Pg diversification, we concluded that the crown eulipotyphlan lineages arose through a rapid diversification after the K-Pg boundary when novel niches were created by the mass extinction of species.
Figure 5 from: Chen Z, Hu T, Pei X, Yang G, Yong F, Xu Z, Qu W, Onditi KO, Zhang B (2022) A new species of Asiatic shrew of the genus Chodsigoa (Soricidae, Eulipotyphla, Mammalia) from the Dabie Mountains, Anhui Province, eastern China. ZooKeys 1083: 129-146. https://doi.org/10.3897/zookeys.1083.78233
Figure 5 - Dorsal and ventral view of Chodsigoa dabieshanensis sp. nov.
Figure 8 from: Bannikova AA, Jenkins PD, Solovyeva EN, Pavlova SV, Demidova TB, Simanovsky SA, Sheftel BI, Lebedev VS, Fang Y, Dalen L, Abramov AV (2019) Who are you, Griselda? A replacement name for a new genus of the Asiatic short-tailed shrews (Mammalia, Eulipotyphla, Soricidae): molecular and morphological analyses with the discussion of tribal affinities. ZooKeys 888: 133-158. https://doi.org/10.3897/zookeys.888.37982
Figure 8 The male karyotype of Parablarinella griselda (ZMMU S-195179) with 2n = 49; NFa = 50.
Figure 6 in Cytogenetic characteristic of the Caucasian pygmy shrew (Sorex volnuchini) and Levant mole (Talpa levantis) (Mammalia: Eulipotyphla) in northern Anatolia, Turkey
Figure 6. Sorex volnuchini NOR bands (female); the arrows show NORs on the chromosomes.
Data from: Post K-Pg diversification of the mammalian order Eulipotyphla as suggested by phylogenomic analyses of ultra-conserved elements
Open the record for dataset details and reuse information.
Figure 6 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
Figure 6. Divergence times estimated using BEAST based on mitochondrial-nuclear concatenated data. Node numbers refer to divergence time in million years (Mya) and Bayesian posterior probabilities (PP).
Figure 4 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
Figure 4. Skins (dorsal view, left and ventral views, right) of the holotype of Alpiscaptulus medogensis (KIZ: 037966).
Figure 3 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
Figure 3. Occlusal views of the right lower teeth and upper teeth of Alpiscaptulus medogensis (KIZ: 037966; A, B) and Scapanulus oweni (KIZ: 033872; C, D). Scale bar = 5 mm.
Figure 2 in Evolutionary history of Sundaland shrews (Eulipotyphla: Soricidae: Crocidura) with a focus on Borneo
Figure 2. Mitochondrial genome maximum-likelihood consensus phylogeny of tropical east Asia Crocidura. Reconstructed with IQTREE. Since most nodes are highly supported [ultrafast bootstrap (UFBP)> 0.95], only less supported nodes are marked (orange circle, 0.95 0.80; green circle, UFBP <0.80). Colours on the vertical bar indicate geographical origin of sampled animals, and colours match the map. Samples from north of the Isthmus of Kra are shown in grey.
Fig. 5 in Whole mitogenomes of Turkish white-toothed shrews, genus Crocidura (Eulipotyphla: Soricidae), with new insights into the phylogenetic positions of Crocidura leucodon and the Crocidura suaveolens group
Fig. 5 Distributional map of taxa within the C. suaveolens group and C. leucodon lineages inferred from CYTB sequences
Figure 6 in Multilocus phylogeny and morphological analyses illuminate overlooked diversity of Soriculus (Mammalia: Eulipotyphla: Soricidae), with descriptions of two new endemic species from the eastern Himalayas
Figure 6. Dorsal, ventral, and lateral views of the skull and lateral view of the mandible of (A) S. nigrescens (MT201904155), (B) S. nivatus (holotype, MT1904951), (C) S. medogensis (holotype, MT201811181), and (D) S. minor (TC-H-KIZ 2345).
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