Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
190
datasets available to search
ShareScore release 0.9.0
Dataset results
190 results for “molecular species delimitation”
Figure 1 from: Ottoni FP, Mattos JLO, Katz AM, Bragança PHN (2019) Phylogeny and species delimitation based on molecular approaches on the species of the Australoheros autrani group (Teleostei, Cichlidae), with biogeographic comments. Zoosystematics and Evolution 95(1): 49-64. https://doi.org/10.3897/zse.95.31658
Figure 1 Map of the samples obtained for the present work. Circles = Australoherosautrani species group; Red circles = Southern Mata Atlântica clade; Yellow circles = Upper/middle Paraíba do Sul river basin and adjacent drainages clade; Green circles – Northern Mata Atlântica clade; and Square = A. sp. Timbé do Sul. Localities: A.autrani = 1 and 18, A.barbosae = 2, 3, 10, 11 and 19, A.ipatinguensis = 4, A.macacuensis = 5, A.macaensis = 6, A.muriae = 9, A.perdi = 12, A.ribeirae = 14, A.robustus = 7, 8, 15, 16 and 20, A.sanguineus = 17, A.cf.capixaba = 13, and A. sp. Timbé do Sul = 21.
Figure 3. A-D in Molecular diversity and species delimitation in the genus Mideopsis Neuman, 1880 in Europe (Acari, Hydrachnidia, Mideopsidae)
Figure 3. A-D Photographs of dorsal shield: A – M. roztoczensis, ♂, CCDB38233 C11, River Zeta, Montenegro. B – M. orbicularis Clade 1, ♂, River Bukowa, Poland. C – M. orbicularis Clade 2, ♀, RMNH.ACA.373, Netherlands. D – M. orbicularis, ♂, Tjeukemeer, Netherlands. E-H Genital field: E – M. roztoczensis, ♂, CCDB38233 C11, Montenegro. F-G – M. orbicularis Clade 1, ♂: F – River Bukowa, Poland; G – RMNH.ACA.374, Netherlands. H-I – M. orbicularis Clade 2, ♀, RMNH.ACA.373, Netherlands. K-O Ejaculatory complex. K – M. roztoczensis, ♂, Roztocze, Poland (from Biesiadka & Kowalik 1979: fig. 10), inset: photograph of anterior ramus, CCDB38233 C11, Montenegro). L – M. orbicularis Clade 1, Roztocze, Poland (from Biesiadka & Kowalik 1979: fig. 12). M – M. orbicularis Clade 1, ♂, River Bukowa, Poland (inset: photograph of anterior ramus). N – M. milankovici, paratype ♂, Montenegro (from Pešić & Smit 2020). O – M. orbicularis, ♂, Tjeukemeer, Netherlands. Scale bars = 100 µm (for K-L = 50 µm).
Figure 2 in Molecular diversity and species delimitation in the genus Mideopsis Neuman, 1880 in Europe (Acari, Hydrachnidia, Mideopsidae)
Figure 2. Minimum Spanning Network showing phylogenetic relationships within three Mideopsis clades: M. roztoczensis, M. orbicularis Clade 1, and M. orbicularis Clade 2. Each bar represents a single mutational change, and a dashed line encircled by separate BINs. The diameter of the circles is proportional to the number of individuals in each haplotype sampled (see open circles with numbers).
FIGURE 2 in Species delimitation in the genus Tamarix: Morphological and molecular data
FIGURE 2. CVA plot of morphological characters for 6 studied Tamarix species.
FIGURE. 1 in Species Delimitation In Rhabdosciadium (Apiaceae): Morphological and Molecular
FIGURE. 1. Distribution map of the populations studied.
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>
FIGURE 3 in Eriocaenus (Acari: Trombidiformes: Eriophyoidea), a new genus from Equisetum spp. (Equisetaceae): morphological and molecular delimitation of two morphologically similar species
FIGURE 3. Semi-schematic drawings of Eriocaenus ramosissimi n. sp.: N. Nymph; L. Larva.
FIGURE 1 in Phylogenetic analyses and species delimitation of Aconurella Ribaut (Hemiptera Cicadellidae: Deltocephalinae: Chiasmini) in China based on molecular data
FIGURE 1. Distribution of sampled specimens of Aconurella in China.
Supplementary material 4 from: Souza CS, Mattox GMT, Vita G, Ochoa LE, Melo BF, Oliveira C (2023) Molecular species delimitation and description of a new species of Phenacogaster (Teleostei, Characidae) from the southern Amazon basin. ZooKeys 1164: 1-21. https://doi.org/10.3897/zookeys.1164.102436
List of the specimens included in the species delimitation analyses
Supplementary material 3 from: Souza CS, Mattox GMT, Vita G, Ochoa LE, Melo BF, Oliveira C (2023) Molecular species delimitation and description of a new species of Phenacogaster (Teleostei, Characidae) from the southern Amazon basin. ZooKeys 1164: 1-21. https://doi.org/10.3897/zookeys.1164.102436
Poisson Tree Processes (PTP) delimitation of species of Phenacogaster
Supplementary material 1 from: Souza CS, Mattox GMT, Vita G, Ochoa LE, Melo BF, Oliveira C (2023) Molecular species delimitation and description of a new species of Phenacogaster (Teleostei, Characidae) from the southern Amazon basin. ZooKeys 1164: 1-21. https://doi.org/10.3897/zookeys.1164.102436
NJ tree of species of Phenacogaster
Data from: Integration of molecular, ecological, morphological and endosymbiont data for species delimitation within the Pnigalio soemius complex (Hymenoptera: Eulophidae)
Open the record for dataset details and reuse information.
Data from: Comparison of methods for molecular species delimitation across a range of speciation scenarios
Open the record for dataset details and reuse information.
Data from: Delimiting species-poor datasets using single molecular markers: a study of barcode gaps, haplowebs and GMYC
Open the record for dataset details and reuse information.
Data from: Species delimitation of the cochineal insects (Dactylopius) using molecular phylogenetics and morphology (Ph.D. thesis)
Open the record for dataset details and reuse information.
Fig. 4 in New Echinoderes (Kinorhyncha: Cyclorhagida) from Mexico: Molecular barcoding demonstrate species delimitation between highly similar morphospecies
Fig. 4. Light micrographs showing overviews and details of (A–I) male holotype, NHMD-920097, and (J) female paratype, NHMD-920098, of Echinoderes abeli sp. nov. from Islas Marias, Mexico. (A) Ventral overview. (B) Segments 1 to 4, ventral view. (C) Segments 1 to 4, dorsal view. (D) Segments 4 to 6, ventral view. (E) Segment 5 to 7, dorsal view. (F) Segments 7 to 10, ventral view. (G) Segments 7 to 8, dorsal view. (H) Detail of segments 10 to 11, ventral view, showing male sexual dimorphism. (I) Detail of segments 10 to 11, dorsal view, showing male sexual dimorphism. (J) Segments 10 to 11, dorsal view, showing female sexual dimorphism. Abbreviations: ldt, laterodorsal tube; ltas, lateral terminal accessory spine; lts, lateral terminal spine; lvs, lateroventral spine; lvt, lateroventral tube; mdgco1, middorsal glandular cell outlet type 1; mds, middorsal spine; pdgco1, paradorsal glandular cell outlet type 1; pe, penile spine; pl placid; pr, protuberance; sdgco2, subdorsal glandular cell outlet type 2; sdss, subdorsal sensory spots; trp, trichoscalid plate. Digits after abbreviations in lvs, lvt and mds refer to segment number.
Fig. 8 in New Echinoderes (Kinorhyncha: Cyclorhagida) from Mexico: Molecular barcoding demonstrate species delimitation between highly similar morphospecies
Fig. 8. Scanning electron micrographs showing overviews and details of Echinoderes wilberti sp. nov. (A) Ventral overview. (B) Segment 1 to 3, ventral view. (C) Segment 4 to 6, ventral view. (D) Segment 8, ventral view. (E) Segments 9 to 10, ventral view. (F) Segment 11, ventral view. (G) Segments 10 to 11, ventral view. (H) Dorsal overview. (I) Segments 1 to 4, dorsal view. (J) Segments 6 to 10, dorsal view. (K) Segments 10 to 11, dorsal view, showing male sexual dimorphism. (L) Segments 10 to 11, dorsal view, showing female sexual dimorphism; inset shows close-up of laterodorsal tube. Abbreviations: lat, lateral accessory tube; ldss, laterodorsal sensory spot; ldt, laterodorsal tube; ltas, lateral terminal accessory spine; lvs, lateroventral spine; lvt, lateroventral tube; mlss, midlateral sensory spot; pe, penile spine; pl, placid; sdss, subdorsal sensory spot; ste, sternal extension; te, tergal extension; vlss, ventrolateral sensory spot; vmss, ventromedial sensory spot. Digits after abbreviations lvs and lvt refer to segment number.
Fig. 7 in New Echinoderes (Kinorhyncha: Cyclorhagida) from Mexico: Molecular barcoding demonstrate species delimitation between highly similar morphospecies
Fig. 7. Light micrographs showing overviews and details of (A–G) female holotype, NHMD-1176454, female paratype (H–I) NHMD-1176456, and (J) male paratype, NHMD-1176455, of Echinoderes wilberti sp. nov. from Xcalak, Quintana Roo, Mexico. (A) Ventral overview. (B) Segments 1 to 2, ventral view. (C) Segments 1 to 2, dorsal view. (D) Segments 3 to 5, ventral view. (E) Segment 3 to 5, dorsal view. (F) Segments 6 to 8, ventral view. (G) Segments 6 to 8, dorsal view. (H) Segments 9 to 11, ventral view. (I) Segments 9 to 11, dorsal view, showing female sexual dimorphism. (J) Segments 10 to 11, dorsal view, showing male sexual dimorphism. Abbreviations: lat, lateral accessory tube, ltas, lateral terminal accessory spine; lts, lateral terminal spine; lvs, lateroventral spine; lvt, lateroventral tube; mdgco1, middorsal glandular cell outlet type 1; pdgco1, paradorsal glandular cell outlet type 1; pe, penile spine; pl placid; pvb, paraventral bristles; sdt, subdorsal tube; ste, sternal extensions; te, tergal extensions; trp, trichoscalid plate; vmgco1, ventromedial glandular cell outlet type 1. Digits after abbreviations lvs and lvt refer to segment number.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.