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.
493
datasets available to search
ShareScore release 0.7.1
Dataset results
493 results for “Rhaphidophoridae”
FIGURE 3 in Contribution to the Chinese subfamily Rhaphidophorinae Walker, 1869 (Orthoptera: Rhaphidophoridae) V: Two new species of Eurhaphidophora
FIGURE 3. Habitus of Eurhaphidophora fossa sp. nov. in lateral view.
Fig. 12 in High alpine sorcerers: revision of the cave wētā genus Pharmacus Pictet & de Saussure (Orthoptera: Rhaphidophoridae: Macropathinae), with the description of six new species and three new subspecies
Fig. 12. Adult female terminalia of cave wētā in the genus Pharmacus Pictet & de Saussure, 1893. Left column: subgenital plate; central and right columns: ovipositor. A–C. Pharmacus montanus Pictet & de Saussure, 1893. A. Mt Annette, Sealy Range, Mt Cook (MPN CW3303). B–C. Mt Wakefield, Mount Cook Range (MPN CW3362). D–F. Pharmacus cochleatus (Karny, 1935) comb. nov., Lochnagar, Richardson Mountains (MPN CW4590). G–I. Pharmacus cristatus sp. nov., Skippers Range High Point, South Westland (NMNZ AI.052293). J–L. Pharmacus notabilis sp. nov., Two Mile Hut, Hector Mountains (NMNZ AI.052297). Scale bars = 1 mm.
FIGURE 4 in Supplement of the genus Diestramima Storozhenko, 1990 (Orthoptera: Rhaphidophoridae: Aemodogryllinae) from China
FIGURE 4. Habitat of Diestramima arbora sp. nov.
MAP 1 in Supplement of the genus Diestramima Storozhenko, 1990 (Orthoptera: Rhaphidophoridae: Aemodogryllinae) from China
MAP 1. Distribution of the genus Diestramima from China.
Fig. 19. Pleioplectron hudsoni Hutton, 1896 in Diversity and distribution of Pleioplectron Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of Weta Chopard and the description of seven new species
Fig. 19. Pleioplectron hudsoni Hutton, 1896. Live specimens in their natural environment. Zealandia Ecosanctuary, Wellington. A. Mating pair. As in most New Zealand Rhaphidophoridae, the female is on top. B. Adult ♀ egg-laying in rotting log.
Fig. 13 in Diversity and distribution of Pleioplectron Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of Weta Chopard and the description of seven new species
Fig. 13. Pleioplectron thomsoni (Chopard, 1923) comb. nov., adult ♂ A. Original drawing by Lucien Chopard (1923), syntype, ♂, Raincliff Reserve, South Canterbury (MNHN EO-ENSIF4924). B. Pioneer Park, South Canterbury (MPN CW3912). Scale bar = 2 mm.
Fig. 14. Live Pleioplectron Hutton, 1896 in Diversity and distribution of Pleioplectron Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of Weta Chopard and the description of seven new species
Fig. 14. Live Pleioplectron Hutton, 1896 in their natural environments. A–B. P. simplex Hutton, 1896, Hinewai Reserve, Banks Peninsula. A. Adult ♀ feeding on a small native snail Flammulina zebra (Le Guillou, 1842). B. Adult ♂. The different colouration is due to individual variation, not sexual dimorphism. C–D. P. thomsoni (Chopard, 1923) comb. nov. C. Adult ♂ in natural cave, Trotters Gorge, Otago. D. Adult ♀ in mining tunnel in Bannockburn, Central Otago, where a population of nearly white colour exists. E. P. hudsoni Hutton, 1896, adult ♀, Otaki Forks, Tararua Forest. F. P. triquetrum sp. nov., ♂, Hinau Track, Kaikōura.
TABLE 1 in Contribution to the Chinese subfamily Rhaphidophorinae Walker, 1869 (Orthoptera: Rhaphidophoridae: Rhaphidophorinae) IV: Seven new species of Rhaphidophora and one new mitogenome
<p>TABLE 1. Annotation and gene organization of the <i>Rhaphidophora quadrispina</i> mitogenome.</p><table><tbody><tr><th>Gene</th><th><b>Strand</b></th><th><b>Location</b></th><th><b>Size (bp)</b></th><th><b>ovl/nc</b></th><th><b>Codons</b></th><th><b>Anticodon</b></th></tr></tbody><tbody><tr><th>trnaI</th><td>J</td><td>1 <b>–</b> 65</td><td>65</td><td>-3</td><td></td><td>GAT</td></tr><tr><th>trnaQ</th><td>N</td><td>63 <b>–</b> 131</td><td>69</td><td>7</td><td></td><td>TTG</td></tr><tr><th>trnaM</th><td>J</td><td>139 <b>–</b> 208</td><td>70</td><td>0</td><td></td><td>CAT</td></tr><tr><th>ND2</th><td>J</td><td>209 <b>–</b> 1237</td><td>1029</td><td>-1</td><td>ATG/TAA</td><td></td></tr><tr><th>trnaW</th><td>J</td><td>1237 <b>–</b> 1303</td><td>67</td><td>-8</td><td></td><td>TCA</td></tr><tr><th>trnaC</th><td>N</td><td>1296 <b>–</b> 1365</td><td>70</td><td>12</td><td></td><td>GCA</td></tr><tr><th>trnaY</th><td>N</td><td>1378 <b>–</b> 1444</td><td>67</td><td>-8</td><td></td><td>GTA</td></tr><tr><th>COI</th><td>J</td><td>1437 <b>–</b> 2981</td><td>1545</td><td>-5</td><td>ATT/TAA</td><td></td></tr><tr><th>trnaL2</th><td>J</td><td>2977 <b>–</b> 3042</td><td>66</td><td>0</td><td></td><td>TAA</td></tr><tr><th>COII</th><td>J</td><td>3043 <b>–</b> 3732</td><td>690</td><td>2</td><td>ATT/TAA</td><td></td></tr><tr><th>trnaR</th><td>J</td><td>3735 <b>–</b> 3804</td><td>70</td><td>-1</td><td></td><td>CTT</td></tr><tr><th>trnaD</th><td>J</td><td>3804 <b>–</b> 3871</td><td>68</td><td>0</td><td></td><td>GTC</td></tr><tr><th>ATP8</th><td>J</td><td>3872 <b>–</b> 4030</td><td><b>159</b></td><td>-7</td><td>ATT/TAA</td><td></td></tr><tr><th>ATP6</th><td>J</td><td>4024 <b>–</b> 4701</td><td>678</td><td>2</td><td>ATG/TAA</td><td></td></tr><tr><th>COIII</th><td>J</td><td>4704 <b>–</b> 5492</td><td>789</td><td>9</td><td>ATG/TAA</td><td></td></tr><tr><th>trnaG</th><td>J</td><td>5502 <b>–</b> 5567</td><td>66</td><td>0</td><td></td><td>TCC</td></tr><tr><th>ND3</th><td>J</td><td>5568 <b>–</b> 5921</td><td>354</td><td>-2</td><td>ATT/TAG</td><td></td></tr><tr><th>trnaA</th><td>J</td><td>5920 <b>–</b> 5983</td><td>64</td><td>-1</td><td></td><td>TGC</td></tr><tr><th>trnaR</th><td>J</td><td>5983 <b>–</b> 6047</td><td>65</td><td>4</td><td></td><td>TCG</td></tr><tr><th>trnaN</th><td>J</td><td>6052 <b>–</b> 6118</td><td>67</td><td>0</td><td></td><td>GTT</td></tr><tr><th>trnaS1</th><td>J</td><td>6119 <b>–</b> 6185</td><td>67</td><td>14</td><td></td><td>GCT</td></tr><tr><th>trnaE</th><td>J</td><td>6200 <b>–</b> 6265</td><td>66</td><td>8</td><td></td><td>TTC</td></tr><tr><th>trnaF</th><td>N</td><td>6264 <b>–</b> 6329</td><td>66</td><td>-3</td><td></td><td>GAA</td></tr><tr><th>ND5</th><td>N</td><td>6327 <b>–</b> 8061</td><td><b>1735</b></td><td>0</td><td><b>GTG</b> /T(AA)</td><td></td></tr><tr><th>trnaH</th><td>N</td><td>8062 <b>–</b> 8125</td><td>64</td><td>3</td><td></td><td>GTG</td></tr><tr><th>ND4</th><td>N</td><td>8129 <b>–</b> 9464</td><td>1336</td><td>-7</td><td>ATG/T(AA)</td><td></td></tr><tr><th>ND4L</th><td>N</td><td>9458 <b>–</b> 9751</td><td>294</td><td>7</td><td>ATG/TAA</td><td></td></tr><tr><th>trnaT</th><td>J</td><td>9759 <b>–</b> 9824</td><td>66</td><td>0</td><td></td><td>TGT</td></tr><tr><th>trnaP</th><td>N</td><td>9825 <b>–</b> 9891</td><td>67</td><td>2</td><td></td><td>TGG</td></tr><tr><th>ND6</th><td>J</td><td>9894 <b>–</b> 10421</td><td>528</td><td>-1</td><td>ATT/TAA</td><td></td></tr><tr><th>CytB</th><td>J</td><td>10421 <b>–</b> 11557</td><td>1137</td><td>2</td><td>ATG/TAA</td><td></td></tr><tr><th>trnaS2</th><td>J</td><td>11560 <b>–</b> 11628</td><td>69</td><td>16</td><td></td><td>TGA</td></tr><tr><th>ND1</th><td>N</td><td>11645 <b>–</b> 12580</td><td>936</td><td>15</td><td>TTG/TAG</td><td></td></tr><tr><th>trnaL1</th><td>N</td><td>12596 -12660</td><td>65</td><td><b>-23</b></td><td></td><td>TAG</td></tr><tr><th>rrnL</th><td>N</td><td>12638 <b>–</b> 13950</td><td>1313</td><td><b>30</b></td><td></td><td></td></tr><tr><th>trnaV</th><td>N</td><td>13981 <b>–</b> 14052</td><td>72</td><td>0</td><td></td><td>TAC</td></tr><tr><th>rrnS</th><td>N</td><td>14053 <b>–</b> 14843</td><td>791</td><td>0</td><td></td><td></td></tr><tr><th>CR</th><td></td><td>14844 <b>–</b> 15892</td><td>1048</td><td></td><td></td><td></td></tr></tbody></table>
TABLE 2 in Contribution to the Chinese subfamily Rhaphidophorinae Walker, 1869 (Orthoptera: Rhaphidophoridae: Rhaphidophorinae) IV: Seven new species of Rhaphidophora and one new mitogenome
<p>TABLE 2. Nucleotide composition and skew of <i>Rhaphidophora quadrispina</i> mitogenome.</p><table><tbody><tr><th></th><th>A%</th><th>T%</th><th>C%</th><th>G%</th><th>A+T%</th><th>AT-skew</th><th>GC-skew</th></tr></tbody><tbody><tr><th>Genome</th><td>41.35</td><td>34.18</td><td>14.84</td><td>9.62</td><td>75.53</td><td>0.09</td><td>-0.21</td></tr><tr><th>PCGs</th><td>40.78</td><td>33.52</td><td>15.40</td><td>10.30</td><td>74.30</td><td>0.10</td><td>-0.20</td></tr><tr><th>PCGs-1st</th><td>37.89</td><td>36.21</td><td>17.10</td><td>8.80</td><td>74.10</td><td><b>0.02</b></td><td>-0.32</td></tr><tr><th>PCGs-2nd</th><td>47.00</td><td>34.15</td><td>11.94</td><td>6.91</td><td>81.15</td><td>0.16</td><td>-0.27</td></tr><tr><th>PCGs-3rd</th><td>37.45</td><td>30.19</td><td>17.16</td><td>15.20</td><td>67.64</td><td>0.11</td><td><b>-0.06</b></td></tr><tr><th>tRNAs</th><td>38.01</td><td>13.33</td><td>37.87</td><td>10.78</td><td><b>51.34</b></td><td><b>0.48</b></td><td><b>-0.56</b></td></tr><tr><th>rRNAs</th><td>44.58</td><td>33.32</td><td>14.40</td><td>7.70</td><td>77.90</td><td>0.14</td><td>-0.30</td></tr><tr><th>CR</th><td>39.94</td><td>41.75</td><td>12.68</td><td>5.62</td><td><b>81.69</b></td><td><b>-0.02</b></td><td>-0.39</td></tr></tbody></table>
Figure 1 in The genus Troglophilus Krauss, 1879 (Orthoptera: Rhaphidophoridae) in the west Balkans
Figure 1. The geographical distribution of the genera Troglophilus and Dolichopoda.
Figure 5 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 5 - Comparison of the autumnal diet between female and male sub-samples of Troglophilus andreinii. Grey: green vegetables; light grey: fibres; black: arthropod remains.
Figure 4 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 4 - Overlap analysis of food resource exploitation conducted in individuals of different age (young instars, nymphs and adults). The dendrograms were performed using euclidean distances based on the Morisita-Horn index matrices. (a: Troglophilus cavicola, b: Troglophilus andreinii).
Figure 3 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 3 - Comparison of the diet among age sub-samples (Young instars, Nymphs and Adults) of Troglophilus cavicola and Troglophilus andreinii. Grey: green vegetables; light grey: fibres; black: arthropod remains.
Figure 2 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 2 - Comparison of seasonal niche breadth in Troglophilus cavicola and Troglophilus andreinii populations
Figure 1 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 1 - Seasonal comparison of food resource exploitation among cumulate samples of Troglophilus cavicola and Troglophilus andreinii. Grey: green vegetables; light grey: fibres; black: arthropod remains.
Figure 22 from: Rampini M, Di Russo C, Taylan M, Gelosa A, Cobolli M (2012) Four new species of Dolichopoda Bolivar, 1880 from Southern Sporades and Western Turkey (Orthoptera, Rhaphidophoridae, Dolichopodainae). ZooKeys 201: 43-58. https://doi.org/10.3897/zookeys.201.2609
Figure 22 - Distribution of troglophilous species of Dolichopoda in Aegean Region. 1 Dolichopoda sutini sp. n. (Sütini cave, Selçuk, İzmir) 2 Dolichopoda giulianae sp. n. (Panaghia Spiliani cave, Pythagorion, Samos) 3 Dolichopoda kalithea sp. n. (Kakoperato cave, Kalithea, M. Kerkis, Samos) 4 Dolichopoda calidnae sp. n. (Seven Virgins cave, Pothia, Kalymnos) 5 Dolichopoda thasosensis (Drakotrypa cave, Thasos) 6 Dolichopoda makrykapa (Piyi Nyphi cave, Makrykapa, Eubea) 7 Dolichopoda cassagnaui (Aghia Trias cave, Karystos, Eubea) 8 Dolichopoda ochtoniai (unnamed cave at North Est of Eubea) 9 Dolichopoda saraolakosi (Lynaria caves, Skyros) 10 Dolichopoda naxia (Za cave, Filotas, Naxos) 11 Dolichopoda paraskevi (Aghia Paraskevi cave, Skotino, Iraklion, Crete).
Figures 11-15 from: Rampini M, Di Russo C, Taylan M, Gelosa A, Cobolli M (2012) Four new species of Dolichopoda Bolivar, 1880 from Southern Sporades and Western Turkey (Orthoptera, Rhaphidophoridae, Dolichopodainae). ZooKeys 201: 43-58. https://doi.org/10.3897/zookeys.201.2609
Figures 11-15 - Dolichopoda kalithea sp. n. Holotype male, 11 X tergite, dorsal view 12 subgenital plate, ventral view 13 epiphallus a dorsal view b lateral view. Female 14 subgenital plate, ventral view 15 ovipositor, lateral view. Scale bars: 1 mm.
Figure 21 from: Rampini M, Di Russo C, Taylan M, Gelosa A, Cobolli M (2012) Four new species of Dolichopoda Bolivar, 1880 from Southern Sporades and Western Turkey (Orthoptera, Rhaphidophoridae, Dolichopodainae). ZooKeys 201: 43-58. https://doi.org/10.3897/zookeys.201.2609
Figure 21 - Dolichopoda calidnae sp. n., holotype male, epiphallus and accessory apparatus a dorsal view b lateral view.
Figures 6-10 from: Rampini M, Di Russo C, Taylan M, Gelosa A, Cobolli M (2012) Four new species of Dolichopoda Bolivar, 1880 from Southern Sporades and Western Turkey (Orthoptera, Rhaphidophoridae, Dolichopodainae). ZooKeys 201: 43-58. https://doi.org/10.3897/zookeys.201.2609
Figures 6-10 - Dolichopoda giulianae sp. n. Holotype male 6 X tergite, dorsal view 7 subgenital plate, ventral view 8 epiphallus, a dorsal view b lateral view. Female 9 subgenital plate, ventral view 10 ovipositor, lateral view. Scale bars: 1 mm.
Figures 1-5 from: Rampini M, Di Russo C, Taylan M, Gelosa A, Cobolli M (2012) Four new species of Dolichopoda Bolivar, 1880 from Southern Sporades and Western Turkey (Orthoptera, Rhaphidophoridae, Dolichopodainae). ZooKeys 201: 43-58. https://doi.org/10.3897/zookeys.201.2609
Figures 1-5 - Dolichopoda sutini sp. n. Holotype male, 1 X tergite, dorsal view 2 subgenital plate, ventral view 3 epiphallus: a- dorsal view, b- lateral view. Female 4 subgenital plate, ventral view 5 ovipositor, lateral view. Scale bars: 1 mm.
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.