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Linked collectors and determiners for: New data on winter crane flies (Diptera: Trichoceridae) of Korea with description of a new species.
Natural history specimen data linked to collectors and determiners held within, "New data on winter crane flies (Diptera: Trichoceridae) of Korea with description of a new species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/fb9d499d-fe53-4f29-b670-2b2bb67d6412">https://bionomia.net/dataset/fb9d499d-fe53-4f29-b670-2b2bb67d6412</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/fb9d499d-fe53-4f29-b670-2b2bb67d6412">https://gbif.org/dataset/fb9d499d-fe53-4f29-b670-2b2bb67d6412</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Studies in Guatemalan Ensifera: New Glaphyrosoma species (Orthoptera: Anostostomatidae) and additional data for other described species.
Natural history specimen data linked to collectors and determiners held within, "Studies in Guatemalan Ensifera: New Glaphyrosoma species (Orthoptera: Anostostomatidae) and additional data for other described species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/b5964523-7b88-4cf5-8400-4d08f276e32e">https://bionomia.net/dataset/b5964523-7b88-4cf5-8400-4d08f276e32e</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/b5964523-7b88-4cf5-8400-4d08f276e32e">https://gbif.org/dataset/b5964523-7b88-4cf5-8400-4d08f276e32e</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: New distribution data for some charismatic tramp species of Platygastroidea (Hymenoptera).
Natural history specimen data linked to collectors and determiners held within, "New distribution data for some charismatic tramp species of Platygastroidea (Hymenoptera)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/7737cac6-f286-4fc1-8494-01c55df12788">https://bionomia.net/dataset/7737cac6-f286-4fc1-8494-01c55df12788</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/7737cac6-f286-4fc1-8494-01c55df12788">https://gbif.org/dataset/7737cac6-f286-4fc1-8494-01c55df12788</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: New data on the irvinei group of Chydaeus of the Himalaya from Nepal and southern Tibet (Coleoptera, Carabidae, Harpalini).
Natural history specimen data linked to collectors and determiners held within, "New data on the irvinei group of Chydaeus of the Himalaya from Nepal and southern Tibet (Coleoptera, Carabidae, Harpalini)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/22bf1c43-357e-4150-af87-98d6e8f5743e">https://bionomia.net/dataset/22bf1c43-357e-4150-af87-98d6e8f5743e</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/22bf1c43-357e-4150-af87-98d6e8f5743e">https://gbif.org/dataset/22bf1c43-357e-4150-af87-98d6e8f5743e</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: New data on Dysdera Latreille, 1804 and Harpactea Bristowe, 1939 (Araneae: Dysderidae) of the Caucasus, with new species and records.
Natural history specimen data linked to collectors and determiners held within, "New data on Dysdera Latreille, 1804 and Harpactea Bristowe, 1939 (Araneae: Dysderidae) of the Caucasus, with new species and records". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/8bf9665f-c622-4b0f-89a4-c79c06bc3ca0">https://bionomia.net/dataset/8bf9665f-c622-4b0f-89a4-c79c06bc3ca0</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/8bf9665f-c622-4b0f-89a4-c79c06bc3ca0">https://gbif.org/dataset/8bf9665f-c622-4b0f-89a4-c79c06bc3ca0</a>. Formatted as a Frictionless Data package.
TABLE 1 in New specimens of Helicops boitata (Serpentes: Dipsadidae: Hydropsini), with data on morphological variation and behavior
<p><b>TABLE 1.</b> Meristic and morphometric variation for all known specimens of <i>Helicops boitata</i>. The asterisk (*) indicate the holotype.</p><table><tbody><tr><th><b>Specimen</b></th><th><b>Sex</b></th><th><b>Total length</b></th><th><b>Tail length</b></th><th><b>Dorsals</b></th><th><b>Ventrals</b></th><th><b>Subcaudals</b></th><th><b>Supralabials</b></th><th><b>Infralabials</b></th><th><b>Temporals</b></th><th><b>Maxillary teeth</b></th><th><b>Cloaca</b></th><th><b>Nasal</b></th></tr></tbody><tbody><tr><th><b>UFMT-R 11490*</b></th><td>Male</td><td>642</td><td>205</td><td>25/25/21</td><td>113</td><td>68</td><td>10/10</td><td>13/12</td><td>2+2+3 / 1+2+3</td><td>20+2</td><td>Entire</td><td>entire</td></tr><tr><th><b>UFMT-R 12504</b></th><td>Male</td><td>495</td><td>143</td><td>25/25/21</td><td>113</td><td>66</td><td>10/10</td><td>12/13</td><td>2+3+4 / 2+4+3</td><td>20+2</td><td>Divided</td><td>Semi-divided</td></tr><tr><th><b>UFMT-R 12505</b></th><td>Female</td><td>383</td><td>86</td><td>25/25/21</td><td>118</td><td>52</td><td>11/10</td><td>13/13</td><td>2+2+3 / 2+2+3</td><td>20+2</td><td>Divided</td><td>Semi-divided</td></tr><tr><th><b>UFMT-R 12506</b></th><td>Male</td><td>598</td><td>177</td><td>23/25/21</td><td>112</td><td>66</td><td>9/10</td><td>12/11</td><td>1+3+3 / 1+2+3</td><td>20+2</td><td>Divided</td><td>Semi-divided</td></tr><tr><th><b>UFMT-R 12520</b></th><td>Female</td><td>618</td><td>153</td><td>25/25/21</td><td>–</td><td>56</td><td>10/10</td><td>13/12</td><td>–</td><td>19+2</td><td>Divided</td><td>Semi-divided</td></tr><tr><th><b>UFMT-R 12521</b></th><td>Male</td><td>639</td><td>197</td><td>25/25/21</td><td>115</td><td>67</td><td>10/10</td><td>13/12</td><td>2+3+5 / 2+3+3</td><td>19+2</td><td>Entire</td><td>Semi-divided</td></tr></tbody></table>
Linked collectors and determiners for: Taxonomy notes and new occurrence data of four species of atyid shrimp (Crustacea: Decapoda: Atyidae) in Vietnam, all described from China.
Natural history specimen data linked to collectors and determiners held within, "Taxonomy notes and new occurrence data of four species of atyid shrimp (Crustacea: Decapoda: Atyidae) in Vietnam, all described from China". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/249ee8b0-183e-418e-8db5-ded1afc3a90b">https://bionomia.net/dataset/249ee8b0-183e-418e-8db5-ded1afc3a90b</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/249ee8b0-183e-418e-8db5-ded1afc3a90b">https://gbif.org/dataset/249ee8b0-183e-418e-8db5-ded1afc3a90b</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: A survey of East Palaearctic Gnaphosidae (Araneae). 11. New data on Gnaphosidae (Araneae) from Tajikistan.
Natural history specimen data linked to collectors and determiners held within, "A survey of East Palaearctic Gnaphosidae (Araneae). 11. New data on Gnaphosidae (Araneae) from Tajikistan". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/311f8acb-781d-4dc3-8d0a-2637317aa691">https://bionomia.net/dataset/311f8acb-781d-4dc3-8d0a-2637317aa691</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/311f8acb-781d-4dc3-8d0a-2637317aa691">https://gbif.org/dataset/311f8acb-781d-4dc3-8d0a-2637317aa691</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Three new species and DNA sequence data of the rare South American water beetle genus Adelphydraena Perkins, 1989 (Coleoptera: Hydraenidae).
Natural history specimen data linked to collectors and determiners held within, "Three new species and DNA sequence data of the rare South American water beetle genus Adelphydraena Perkins, 1989 (Coleoptera: Hydraenidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/fa172759-c7a8-4682-b992-8871c155eb3a">https://bionomia.net/dataset/fa172759-c7a8-4682-b992-8871c155eb3a</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/fa172759-c7a8-4682-b992-8871c155eb3a">https://gbif.org/dataset/fa172759-c7a8-4682-b992-8871c155eb3a</a>. Formatted as a Frictionless Data package.
FIGURE 23 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
FIGURE 23. Ecological nische suitability map, described by predictable variables; bio8 and bio14.
TABLE 7 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 7</b>. Spectral parameters belong to male calling songs of <i>Anadolua shcwarzi</i>, <i>A. moli</i> <b>sp. nov.</b> and <i>A. bergeri</i> <b>sp. nov.</b> populations.</p><table><tbody><tr><th><b>Taxon (Location) / Range (min–max) m ± sd n</b></th><th><b>FS-DF kHz</b></th><th><b>FS-PF kHz</b></th><th><b>RS-DF kHz</b></th><th><b>RS-PF kHz</b></th></tr><tr><th><b><i>Anadolua bergeri</i> sp. nov.</b></th></tr></tbody><tbody><tr><th>Konya, Rezebeli (N=3)</th><td>23.55–39.67 30.85 ± 5.04 13</td><td>20.25–30.75 24.20 ± 3.15 13</td><td>42.60–54.38 49.95 ± 3.76 13</td><td>19.13–31.50 27.03 ± 4.09 13</td></tr><tr><th>Antalya, GündoğmuŞ (N=1)</th><td>24.00–31.30 27.70 ± 2.68 5</td><td>25.50–33.00 29.18 ± 3.48 5</td><td>37.00–43.14 40.55 ± 2.74 5</td><td>25.13–28.88 27.60 ± 1.58 5</td></tr></tbody></table><p>......continued on the next page</p>
TABLE 6 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 6</b>. Temporal parameters measured from male calling songs of <i>Anadolua shcwarzi</i>, <i>Anadolua moli</i> <b>sp. nov.</b> <i>Anadolua bergeri</i> <b>sp. nov.</b> populations.</p><table><tbody><tr><th><b>Taxon (Location) Range m ± sd n</b></th><th><b>Song=Phrase Duration (s)</b></th><th><b>Syllables Group per phrase</b></th><th><b>Double Syllables Group Duration (ms)</b></th><th><b>Triple Syllables Group Duration (ms)</b></th><th><b>First Low amplitude Syllable Duration (ms)</b></th><th><b>First Syllable Duration (ms)</b></th><th><b>Second Syllable Duration (ms)</b></th><th><b>Third Syllable Duration (ms)</b></th></tr><tr><th><b><i>Anadolua moli</i> sp. nov.</b></th></tr></tbody><tbody><tr><th>Konya, Sultandağ (N=3)</th><td>3.12–17.21 6.63 ± 3.15 20</td><td>33–171 67 ± 30.4 20</td><td>87.7–164.2 104.10 ± 8.16 260</td><td>-</td><td>72.23–134.00 110.08 ± 19.35 13</td><td>23.05–47.40 28.45 ± 4.64 260</td><td>28.50–43.00 32.57 ± 3.53 260</td><td>--</td></tr><tr><th><i>Anadolua schwarzi</i></th></tr><tr><th><i>Muğla, Sandras</i> (N=4)</th><td>5.83–62.87 29.47 ± 17.47 11</td><td>30–273 156.00 ± 81.35 11</td><td>-</td><td>163.50–230.02 178.95 ± 13.76 100</td><td>273.12–520.05 417.33 ± 96.44 11</td><td>23.50–27.60 25.81 ± 1.05 100</td><td>23.20–30.40 26.25 ± 1.85 100</td><td>24.50–32.30 28.45 ± 1.86 100</td></tr><tr><th><i>Denizli-Babadağ</i> (N=6)</th><td>2.93–23.07 10.39 ± 5.99 14</td><td>16–126 52.64 ± 33.30 14</td><td>-</td><td>182.90–272.90 210.67 ± 10.45 120</td><td>226.60–344.90 269.32 ± 43.54 14</td><td>27.70–38.20 31.84 ± 2.55 120</td><td>30.20–35.10 32.42 ± 1.58 120</td><td>29.00–37.30 33.36 ± 2.41 120</td></tr><tr><th><i>İzmir-Bozdağ</i> (N=3)</th><td>4.55–24.76 13.87 ± 5.46 16</td><td>23–128 70.19 ± 29.01 16</td><td>-</td><td>191.70–214.60 199.46 ± 5.96 130</td><td>179.23–405.24 291.43 ± 85.84 16</td><td>29.60–40.50 34.78 ± 2.14 130</td><td>34.90–40.50 37.59 ± 1.45 130</td><td>36.60–46.60 40.09 ± 1.81 130</td></tr><tr><th><i>Antalya-Gömbe-I</i> (N=1)</th><td>8.25–22.24 12.92 ± 5.57 5</td><td>58–152 86.20 ± 38.69 5</td><td>-</td><td>142.40–179.70 157.72 ± 12.09 40</td><td>170.33–389.65 247.51 ± 86.30 5</td><td>23.50–27.60 25.17 ± 1.26 40</td><td>22.50–28.70 24.93 ± 1.27 40</td><td>20.40–25.90 28.70 ± 1.74 40</td></tr><tr><th><i>Antalya-Gömbe-II</i> (N=1)</th><td>6.46–60.95 26.69 ± 17.36 11</td><td>39–353 150.18 ± 96.19 11</td><td>-</td><td>154.20–203.90 173.30 ± 11.02 110</td><td>170.33–443.40 243.55 ± 99.31 11</td><td>22.60–27.50 24.70 ± 1.16 110</td><td>22.90–27.30 25.43 ± 1.17 110</td><td>25.90–32.70 29.71 ± 1.94 110</td></tr><tr><th><i>Antalya-Tahtalıdağ</i> (N=1)</th><td>21.66–111.96 52.49 ± 51.50 3</td><td>135–702 427.57 ± 127.98 3</td><td>-</td><td>146.80–175.60 156.52 ± 4.94 30</td><td>348.00–575.20 427.57 ± 127.99 3</td><td>21.90–26.20 23.92 ± 1.28 30</td><td>19.60–27.10 22.52 ± 2.34 30</td><td>21.50–28.90 25.29 ± 1.51 30</td></tr><tr><th><i>Uşak-Şaphane</i> (N=2)</th><td>5.20–24.22 12.40 ± 7.11 13</td><td>37–180 92.82 ± 54.66 13</td><td>-</td><td>125.60–185.60 142.76 ± 14.79 130</td><td>140.20–276.10 171.20 ± 60.41 5</td><td>22.30–29.20 25.67 ± 1.96 130</td><td>22.90–30.08 26.23 ± 2.38 130</td><td>24.00–35.50 29.28 ± 2.93 130</td></tr><tr><th><i>Kütahya-Civanağa</i> (N=2)</th><td>7.17–23.06 16.39 ± 5.47 8</td><td>56–177 124.00 ± 41.57 8</td><td>-</td><td>130.20–179.30 141.13 ± 9.85 80</td><td>142.10–291.30 124.20 ± 60.01 6</td><td>21.90–28.00 24.51 ± 1.69 80</td><td>23.80–31.10 27.26 ± 1.49 80</td><td>27.20–33.10 30.02 ± 1.43 80</td></tr><tr><th><b>Taxon (Location) Range m ± sd n</b></th><td><b>Song=Phrase Duration (s)</b></td><td><b>Syllables per phrase</b></td><td><b>Syllables Duration (ms)</b></td><td><b>First Low amplitude Syllable Duration (ms)</b></td><td><b>Opening Hemi Syllable Durations (ms)</b></td><td><b>Closing Hemi Syllable Durations (ms)</b></td><td></td><td></td></tr><tr><th><b><i>Anadolua bergeri</i> sp. nov.</b></th></tr><tr><th>Konya, Rezebeli (N=3)</th><td>0.598–0.864 0.710 ± 0.05 18</td><td>17–21 18.46 ± 0.97 18</td><td>28.80–45.20 39.81 ± 2.96 180</td><td>18.10–21.50 19.62 ± 1.16 18</td><td>6.90–17.62 9.81 ± 1.17 180</td><td>19.00–34.60 29.98 ± 2.31 180</td><td></td><td></td></tr><tr><th>Antalya,GündoğmuŞ (N=1)</th><td>0.484–0.556 0.509 ± 0.03 5</td><td>17–21 18.46 ± 0.97 5</td><td>29.10–38.90 35.45 ± 2.41 50</td><td>16.60–19.10 17.88 ± 1.15 5</td><td>7.60–13.00 9.86 ± 1.32 50</td><td>23.00–30.30 26.89 ± 1.58 50</td><td></td><td></td></tr></tbody></table><p>......continued on the next page</p><p>Range (minimum–maximum); m—Mean; sd—Standard deviation; n—Number of the analyzed characters; N=Number of song recorded males.</p>
TABLE 3. Means and standard deviations for 16 morphometric characters measured from males representing 12 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 3</b>. Means and standard deviations for 16 morphometric characters measured from males representing 12 populations belonging to <i>Anadolua</i> genus.</p><table><tbody><tr><th><b>Localities</b></th><th></th><th></th><th></th><th></th><th></th><th></th><th></th><th><b>Characters</b></th><th></th><th></th><th></th><th></th><th></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td></td><td></td><td></td><td></td><td></td><td></td><td>(m ± sd, except NSF)</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>TLB</td><td>TL</td><td>TLP</td><td>MIDLC</td><td>MADLC</td><td>LHF</td><td>MWHF</td><td>MWFS</td><td>MLS</td><td>MWS</td><td>MWBE</td><td>MLAT</td><td>MWAT</td><td>MLC</td><td>LCMIT</td><td>NSF</td></tr><tr><th><i>A. schwarzi</i> (Muğla-Sandras) N=4</th><td>26.40 ±0.59</td><td>5.26 ±0.11</td><td>7.09 ±0.09</td><td>1.72 ±0.13</td><td>4.79 ±0.09</td><td>18.90 ±0.67</td><td>4.05 ±0.13</td><td>1.06 ±0.01</td><td>0.99 ±0.04</td><td>0.84 ±0.00</td><td>2.41 ±0.05</td><td>1.44 ±0.11</td><td>1.06 ±0.02</td><td>1.80 ±0.02</td><td>0.64 ±0.03</td><td>66.75 ±3.09</td></tr><tr><th><i>A. schwarzi</i> (Denizli-Babadağ) N=10</th><td>23.47 ±1.46</td><td>5.50 ±0.13</td><td>6.30 ±0.10</td><td>1.60 ±0.12</td><td>4.93 ±0.19</td><td>18.57 ±0.40</td><td>3.87 ±0.16</td><td>1.04 ±0.05</td><td>1.04 ±0.01</td><td>0.91 ±0.06</td><td>2.28 ±0.05</td><td>1.42 ±0.09</td><td>0.88 ±0.04</td><td>1.69 ±0.08</td><td>0.52 ±0.02</td><td>65.00 ±2.71</td></tr><tr><th><i>A. schwarzi</i> (İzmir-Bozdağ) N=5</th><td>20.84 ±0.71</td><td>5.37 ±0.14</td><td>6.84 ±0.18</td><td>1.83 ±0.12</td><td>5.08 ±0.08</td><td>18.50 ±0.38</td><td>3.96 ±0.11</td><td>1.00 ±0.08</td><td>1.10 ±0.05</td><td>0.83 ±0.02</td><td>2.43 ±0.07</td><td>1.40 ±0.12</td><td>0.85 ±0.85</td><td>1.63 ±0.09</td><td>0.65 ±0.07</td><td>65.60 ±3.21</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_I) N=3</th><td>22.33 ±1.04</td><td>4.76 ±0.09</td><td>6.18 ±0.13</td><td>1.53 ±0.05</td><td>4.72 ±0.13</td><td>18.60 ±0.96</td><td>3.60 ±0.20</td><td>0.91 ±0.06</td><td>1.00 ±0.05</td><td>0.84 ±0.05</td><td>2.19 ±0.08</td><td>1.34 ±0.07</td><td>0.74 ±0.09</td><td>1.74 ±0.07</td><td>0.54 ±0.04</td><td>70.00 ±3.60</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_II) N=4</th><td>20.92 ±1.11</td><td>4.82 ±0.10</td><td>6.34 ±0.09</td><td>1.65 ±0.19</td><td>4.89 ±0.16</td><td>18.62 ±0.29</td><td>3.95 ±0.19</td><td>0.93 ±0.03</td><td>1.01 ±0.05</td><td>0.90 ±0.03</td><td>2.22 ±0.07</td><td>1.35 ±0.03</td><td>0.85 ±0.03</td><td>1.71 ±0.03</td><td>0.48 ±0.01</td><td>67.75 ±4.35</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Tahtalıdağ) N=1</th><td>24.40</td><td>5.14</td><td>6.84</td><td>1.84</td><td>4.84</td><td>18.30</td><td>3.90</td><td>1.06</td><td>0.96</td><td>0.84</td><td>2.37</td><td>1.57</td><td>1.00</td><td>1.92</td><td>0.56</td><td>74.00</td></tr><tr><th><i>A. schwarzi</i> (UŞak-Şaphane) N=6</th><td>19.87 ±1.48</td><td>4.81 ±0.14</td><td>6.26 ±0.24</td><td>1.79 ±0.07</td><td>4.79 ±0.19</td><td>18.83 ±0.40</td><td>3.63 ±0.10</td><td>0.97 ±0.02</td><td>1.14 ±0.06</td><td>0.84 ±0.04</td><td>2.10 ±0.06</td><td>1.41 ±0.12</td><td>0.98 ±0.08</td><td>1.77 ±0.10</td><td>0.59 ±0.04</td><td>64.00 ±3.16</td></tr><tr><th><i>A. schwarzi</i> (Kütahya-Civanağa) N=4</th><td>21.17 ±0.89</td><td>5.35 ±0.14</td><td>6.36 ±0.16</td><td>1.72 ±0.11</td><td>4.94 ±0.10</td><td>18.00 ±0.82</td><td>3.42 ±0.15</td><td>0.96 ±0.02</td><td>1.07 ±0.05</td><td>0.71 ±0.03</td><td>2.17 ±0.09</td><td>1.37 ±0.03</td><td>1.02 ±0.09</td><td>1.65 ±0.05</td><td>0.57 ±0.01</td><td>62.2 ±2.22</td></tr><tr><th><i>A. schwarzi</i> (Denizli Çameli) N=5</th><td>22.32 ±4.16</td><td>5.44 ±0.12</td><td>6.81 ±0.15</td><td>1.63 ±0.03</td><td>5.12 ±0.13</td><td>18.98 ±1.24</td><td>4.00 ±0.19</td><td>0.98 ±0.03</td><td>1.13 ±0.03</td><td>0.79 ±0.03</td><td>2.28 ±0.03</td><td>1.45 ±0.06</td><td>0.88 ±0.04</td><td>1.62 ±0.04</td><td>0.57 ±0.01</td><td>64.00 ±3.67</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Konya-Rezebeli) N=4</th><td>22.62 ±1.11</td><td>5.36 ±0.30</td><td>6.43 ±0.30</td><td>2.20 ±0.09</td><td>4.84 ±0.27</td><td>17.27 ±0.48</td><td>4.00 ±0.09</td><td>1.04 ±0.07</td><td>1.13 ±0.07</td><td>0.89 ±0.10</td><td>2.43 ±0.05</td><td>1.33 ±0.11</td><td>1.44 ±0.05</td><td>2.22 ±0.16</td><td>0.87 ±0.06</td><td>46.00 ±1.82</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Antalya-GündoğmuŞ) N=1</th><td>24.00</td><td>5.32</td><td>6.63</td><td>2.21</td><td>4.89</td><td>16.60</td><td>4.00</td><td>0.95</td><td>1.05</td><td>0.84</td><td>2.58</td><td>1.28</td><td>1.19</td><td>2.31</td><td>0.97</td><td>49.00</td></tr><tr><th><i>A. moli</i> <b>sp. nov.</b> (Konya-Sultandağ) N=5</th><td>21.90 ±1.51</td><td>4.72 ±0.08</td><td>6.28 ±0.09</td><td>1.81 ±0.04</td><td>4.59 ±0.10</td><td>17.80 ±0.45</td><td>3.74 ±0.17</td><td>0.93 ±0.05</td><td>1.12 ±0.06</td><td>0.87 ±0.05</td><td>2.24 ±.06</td><td>1.71 ±0.16</td><td>1.14 ±0.05</td><td>1.33 ±0.11</td><td>0.65 ±0.03</td><td>51.80 ±2.39</td></tr></tbody></table><p>m—Mean; sd—Standard deviation; N—individuals</p>
TABLE 9 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 9</b>. Percentage contributions of bioclimatic variables in different model algorithms.</p><table><tbody><tr><th><b>Bioclimatic variables</b></th><th><b>Code</b></th><th><b>Model’s Percentage contributions based on AUC metric (%)</b></th></tr></tbody><tbody><tr><th></th><td></td><td>GLM</td><td>FD</td><td>MARS</td><td>RF</td><td>MAXENT</td></tr><tr><th>Annual mean temperature</th><td>bio1</td><td>8.9</td><td>7.4</td><td>10.4</td><td>2.1</td><td>0.4</td></tr><tr><th>Isothermality (BIO2/BIO7) (×100)</th><td>bio3</td><td>5.7</td><td>4.2</td><td>9.9</td><td>1.5</td><td>2.6</td></tr><tr><th>Temperature Seasonality (standard deviation ×100)</th><td>bio4</td><td>13.2</td><td>7.1</td><td>30.7</td><td>3.2</td><td>4.1</td></tr><tr><th>Mean Temperature of Wettest Quarter</th><td>bio8</td><td>44</td><td>49</td><td>23.7</td><td>31.8</td><td>50.9</td></tr><tr><th>Precipitation of Driest Month</th><td>bio14</td><td>19.5</td><td>5.3</td><td>18.3</td><td>6.5</td><td>13.9</td></tr><tr><th>Precipitation Seasonality (Coefficient of Variation)</th><td>bio15</td><td>7.7</td><td>15</td><td>27.5</td><td>3.8</td><td>5.3</td></tr></tbody></table>
TABLE 1. 13 bioclimatic variables from the 19 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 1</b>. 13 bioclimatic variables from the 19 input variables have collinearity problem. After excluding the collinear variables, the linear correlation coefficient ranges between min correlation (bio8~bio4). -0.0037, max correlation (bio4~bio14): -0.783.Descriptive statistics for morphological measurements of the both sexes (mean and standard error).</p><table><tbody><tr><th>Variables</th><th>VIF</th></tr></tbody><tbody><tr><th>Bio1</th><td>3.345</td></tr><tr><th>Bio3</th><td>2.703</td></tr><tr><th>Bio4</th><td>5.227</td></tr><tr><th>Bio8</th><td>3.195</td></tr><tr><th>Bio14</th><td>6.855</td></tr><tr><th>Bio15</th><td>2.475</td></tr></tbody></table>
TABLE 5. Means and standard deviations for 15 morphometric characters measured from females representing 10 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 5</b>. Means and standard deviations for 15 morphometric characters measured from females representing 10 populations belonging to <i>Anadolua</i> species.</p><table><tbody><tr><th><b>Characters</b> (mm ± sd)</th></tr></tbody><tbody><tr><th><b>Localities</b></th><td>TLB</td><td>TLP</td><td>MIDLC</td><td>MADLC</td><td>MLHF</td><td>MWHF</td><td>MWFS</td><td>MLS</td><td>MWS</td><td>MWBE</td><td>MLAT</td><td>MWAT</td><td>MLC</td><td>MLO</td><td>MWO</td></tr><tr><th><i>A. schwarzi</i> (Muğla-Sandras) N=3</th><td>25.66 ±1.52</td><td>7.37 ±0.19</td><td>1.96 ±0.08</td><td>5.40 ±0.16</td><td>24.00 ±3.00</td><td>4.33 ±0.15</td><td>1.16 ±0.05</td><td>1.14 ±0.02</td><td>0.89 ±0.05</td><td>2.66 ±0.08</td><td>1.08 ±0.05</td><td>0.27 ±0.02</td><td>1.63 ±0.04</td><td>21.06 ±0.40</td><td>1.90 ±0.10</td></tr><tr><th><i>A. schwarzi</i> (Denizli-Babadağ) N=6</th><td>25.00 ±2.61</td><td>6.96 ±0.25</td><td>2.06 ±0.13</td><td>5.29 ±0.21</td><td>19.83 ±1.25</td><td>4.15 ±0.26</td><td>1.08 ±0.03</td><td>1.30 ±0.09</td><td>0.92 ±0.03</td><td>2.46 ±0.12</td><td>1.15 ±0.07</td><td>0.26 ±0.02</td><td>1.43 ±0.04</td><td>19.80 ±1.58</td><td>1.96 ±0.08</td></tr><tr><th><i>A. schwarzi</i> (İzmir-Bozdağ) N=8</th><td>24.90 ±1.15</td><td>7.89 ±0.31</td><td>2.08 ±0.10</td><td>5.54 ±0.15</td><td>22.00 ±1.00</td><td>4.76 ±0.39</td><td>1.16 ±0.06</td><td>1.13 ±0.09</td><td>0.88 ±0.03</td><td>2.72 ±0.14</td><td>1.06 ±0.07</td><td>0.29 ±0.06</td><td>1.50 ±0.06</td><td>21.81 ±0.55</td><td>2.20 ±0.29</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_I) N=2</th><td>23.75 ±0.64</td><td>6.45 ±0.41</td><td>2.00 ±0.07</td><td>5.37 ±0.30</td><td>18.50 ±0.71</td><td>3.90 ±0.00</td><td>1.08 ±0.04</td><td>1.29 ±0.04</td><td>0.84 ±0.07</td><td>2.31 ±0.08</td><td>0.92 ±0.00</td><td>0.32 ±0.01</td><td>1.44 ±0.00</td><td>20.20 ±0.00</td><td>2.00 ±0.00</td></tr><tr><th>A. schwarzi (Antalya-Gömbe_II) N=6</th><td>21.07 ±3.37</td><td>6.28 ±0.41</td><td>1.73 ±0.20</td><td>4.62 ±0.22</td><td>17.67 ±0.42</td><td>3.90 ±0.18</td><td>0.98 ±0.05</td><td>1.09 ±0.04</td><td>0.83 ±0.04</td><td>2.27 ±0.17</td><td>0.94 ±0.06</td><td>0.37 ±0.04</td><td>1.28 ±0.08</td><td>18.41 ±0.58</td><td>2.03 ±0.05</td></tr><tr><th><i>A. schwarzi</i> (UŞak-Şaphane) N=4</th><td>21.70 ±0.57</td><td>6.60 ±0.21</td><td>1.89 ±0.04</td><td>5.14 ±0.20</td><td>20.60 ±0.36</td><td>3.85 ±0.06</td><td>1.06 ±0.03</td><td>1.28 ±0.09</td><td>0.92 ±0.03</td><td>2.43 ±0.03</td><td>1.09 ±0.07</td><td>0.36 ±0.07</td><td>1.22 ±0.03</td><td>22.02 ±0.83</td><td>2.17 ±0.09</td></tr><tr><th><i>A. schwarzi</i> (Kütahya-Civanağa) N=3</th><td>22.33 ±1.15</td><td>6.82 ±0.29</td><td>2.16 ±0.19</td><td>5.04 ±0.28</td><td>18.17 ±0.80</td><td>3.63 ±0.35</td><td>1.05 ±0.00</td><td>1.26 ±0.05</td><td>0.91 ±0.03</td><td>2.45 ±0.03</td><td>0.93 ±0.04</td><td>0.48 ±0.03</td><td>1.28 ±0.05</td><td>19.47 ±0.47</td><td>2.13 ±0.06</td></tr><tr><th><i>A. schwarzi</i> (Denizli Çameli) N=5</th><td>23.04 ±1.51</td><td>7.50 ±0.30</td><td>2.16 ±0.20</td><td>5.61 ±0.11</td><td>21.54 ±0.93</td><td>4.54 ±0.29</td><td>1.09 ±0.03</td><td>1.33 ±0.04</td><td>0.95 ±0.05</td><td>2.62 ±0.09</td><td>1.19 ±0.06</td><td>0.19 ±0.04</td><td>1.40 ±0.02</td><td>22.04 ±1.65</td><td>2.06 ±0.11</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Konya-Rezebeli) N=3</th><td>22.73 ±0.64</td><td>5.80 ±0.16</td><td>1.60 ±0.06</td><td>4.19 ±0.08</td><td>15.97 ±0.15</td><td>3.97 ±0.06</td><td>0.89 ±0.00</td><td>1.09 ±0.03</td><td>0.79 ±0.00</td><td>2.24 ±0.03</td><td>0.80 ±0.04</td><td>0.28 ±0.03</td><td>1.22 ±0.05</td><td>13.97 ±0.15</td><td>1.80 ±0.10</td></tr><tr><th><i>A. moli</i> <b>sp. nov.</b> (Konya-Sultandağ) N=6</th><td>22.25 ±1.17</td><td>6.98 ±0.22</td><td>2.22 ±0.14</td><td>5.22 ±0.16</td><td>20.95 ±0.83</td><td>4.02 ±0.19</td><td>1.10 ±0.06</td><td>1.28 ±0.03</td><td>0.81 ±0.04</td><td>2.49 ±0.07</td><td>1.12 ±0.05</td><td>0.43 ±0.03</td><td>1.45 ±0.07</td><td>21.59 ±1.11</td><td>2.08 ±0.10</td></tr></tbody></table><p>m—Mean; sd—Standard deviation; N—individuals</p>
TABLE 4 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 4</b>. Factors, eigenvalues and cumulative percentages obtained by factor analysis of 16 morphological characters from the males of <i>Anadolua shcwarzi</i> (9 populations), <i>Anadolua moli</i> <b>sp. nov.</b> (1 population), <i>Anadolua bergeri</i> <b>sp. nov.</b> (2 populations).</p><table><tbody><tr><th>Characters</th><th>Factor 1</th><th>Factor 2</th><th>Factor 3</th><th>Factor 4</th><th>Factor 5</th></tr></tbody><tbody><tr><th>LCMIT</th><td>. <b>933</b> a</td><td>.204</td><td>.024</td><td>-.009</td><td>-.050</td></tr><tr><th>MWAT</th><td>. <b>905</b> a</td><td>-.100</td><td>-.072</td><td>.128</td><td>.087</td></tr><tr><th>MIDLC</th><td>. <b>852</b> a</td><td>.157</td><td>-.181</td><td>-.115</td><td>-.072</td></tr><tr><th>NSF</th><td><b>-.818</b> a</td><td>.150</td><td>.217</td><td>.051</td><td>-.098</td></tr><tr><th>MLC</th><td>. <b>754</b> a</td><td>.244</td><td>.450</td><td>.008</td><td>.162</td></tr><tr><th>MLHF</th><td>-.550</td><td>.418</td><td>-.406</td><td>.435</td><td>.124</td></tr><tr><th>TL</th><td>-.004</td><td>. <b>798</b> a</td><td>.074</td><td>-.182</td><td>.039</td></tr><tr><th>MADLC</th><td>.051</td><td>. <b>797</b> a</td><td>.105</td><td>.187</td><td>-.140</td></tr><tr><th>TLP</th><td>-.182</td><td>. <b>714</b> a</td><td>-.282</td><td>-.190</td><td>-.222</td></tr><tr><th>MWHF</th><td>.129</td><td>. <b>617</b> a</td><td>.087</td><td>.088</td><td>.530</td></tr><tr><th>MWBE</th><td>.493</td><td>. <b>607</b> a</td><td>.368</td><td>-.016</td><td>.205</td></tr><tr><th>MWFS</th><td>.101</td><td>.547</td><td>.135</td><td>.330</td><td>.232</td></tr><tr><th>MLS</th><td>.374</td><td>-.007</td><td><b>-.829</b> a</td><td>-.014</td><td>.008</td></tr><tr><th>MLAT</th><td>-.079</td><td>.034</td><td>-.024</td><td>. <b>894</b> a</td><td>-.097</td></tr><tr><th>TLB</th><td>.114</td><td>.353</td><td>.481</td><td>.531</td><td>.114</td></tr><tr><th>MWS</th><td>.004</td><td>-.062</td><td>.004</td><td>-.063</td><td>. <b>944</b> a</td></tr><tr><th>Eigenvalue</th><td>4.623</td><td>3.106</td><td>1.609</td><td>1.244</td><td>1.179</td></tr><tr><th>Cumulative %</th><td>30.823</td><td>51.532</td><td>62.260</td><td>70.553</td><td>78.412</td></tr></tbody></table><p><sup>a</sup> Factor loadings considered to be important to each factor.</p>
Data from: Host associations and beta diversity of fungal endophyte communities in New Guinea rainforest trees
Processes shaping the distribution of foliar fungal endophyte species remain poorly understood. Despite increasing evidence that these cryptic fungal symbionts of plants mediate interactions with pathogens and herbivores, there remain basic questions regarding the extent to which dispersal limitation and host specificity might shape fungal endophyte community composition in rainforests. To assess the relative importance of spatial pattern and host specificity, we isolated fungi from a sample of mapped trees in lowland Papua New Guinea. Sequences of the internal transcribed spacer (ITS) region were obtained for 2,079 fungal endophytes from three sites and clustered into molecular operational taxonomic units (MOTUs) at 95% similarity. Multivariate analyses suggest that host affinity plays a significant role in structuring endophyte community composition whereas there was no evidence of endophyte spatial pattern at the scale of tens to hundreds of meters. Differences in endophyte communities between sampled trees were weakly correlated with variation in foliar traits but not with tree species relatedness. The dominance of relatively few generalist endophytes and the presence of a large number of rare MOTUs was a consistent observation at three sites separated by hundreds of kilometers and regional turnover was low. Host specificity appears to play a relatively weak but more important role than dispersal limitation in shaping the distribution of fungal endophyte communities in New Guinea forests. Our results suggest that in the absence of strong ecological gradients and host turnover, beta diversity of endophyte communities could be low in large areas of contiguous forest.
Data from: A new method of Bayesian causal inference in non-stationary environments
Bayesian inference is the process of narrowing down the hypotheses (causes) to the one that best explains the observational data (effects). To accurately estimate a cause, a considerable amount of data is required to be observed for as long as possible. However, the object of inference is not always constant. In this case, a method such as exponential moving average (EMA) with a discounting rate is used to improve the ability to respond to a sudden change; it is also necessary to increase the discounting rate. That is, a trade-off is established in which the followability is improved by increasing the discounting rate, but the accuracy is reduced. Here, we propose an extended Bayesian inference (EBI), wherein human-like causal inference is incorporated. We show that both the learning and forgetting effects are introduced into Bayesian inference by incorporating the causal inference. We evaluate the estimation performance of the EBI through the learning task of a dynamically changing Gaussian mixture model. In the evaluation, the EBI performance is compared with those of the EMA and a sequential discounting expectation-maximization algorithm. The EBI was shown to modify the trade-off observed in the EMA.
Data from: The genetic architecture of constitutive and induced trichome density in two new RIL populations of Arabidopsis thaliana: phenotypic plasticity, epistasis, and bidirectional leaf damage response
Background: Herbivory imposes an important selective pressure on plants. In Arabidopsis thaliana leaf trichomes provide a key defense against insect herbivory; however, trichome production incurs a fitness cost in the absence of herbivory. Previous work on A. thaliana has shown an increase in trichome density in response to leaf damage, suggesting a mechanism by which the cost associated with constitutively high trichome density might be mitigated; however, the genetic basis of trichome density induction has not been studied. Results: Here, we describe the mapping of quantitative trait loci (QTL) for constitutive and damage induced trichome density in two new recombinant inbred line populations of A. thaliana; mapping for constitutive and induced trichome density also allowed for the investigation of damage response (plasticity) QTL. Both novel and previously identified QTL for constitutive trichome density and the first QTL for induced trichome density and response are identified. Interestingly, two of the four parental accessions and multiple RILs in each population exhibited lower trichome density following leaf damage, a response not previously described in A. thaliana. Importantly, a single QTL was mapped for the response phenotype and allelic variation at this locus appears to determine response trajectory in RILs. The data also show that epistatic interactions are a significant component of the genetic architecture of trichome density. Conclusions: Together, our results provide further insights into the genetic architecture of constitutive trichome density and new insights into induced trichome density in A. thaliana specifically and to our understanding of the genetic underpinnings of natural variation generally.
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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.