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FIGURE 2 in Entoloma chamaemori (Entolomataceae, Basidiomycota)-a new boreal species, with isolated phylogenetic position
FIGURE 2. Entoloma chamaemori. Holotype in situ. Photo Jostein Lorås
FIGURE 3 in Entoloma chamaemori (Entolomataceae, Basidiomycota)-a new boreal species, with isolated phylogenetic position
FIGURE 3. Entoloma chamaemori. Habitat in Holmvassdalen Nature Reserve. Photo Jostein Lorås.
FIGURE 1 in Nomenclatural and taxonomic notes on Acroglochin and its position in Chenopodiaceae s.str.
FIGURE 1. Lectotype of Acroglochin chenopodioides (LE-00018195!).
FIGURE 4 in Allium istanbulense, a new autumnal species of A. sect. Codonoprasum (Amaryllidaceae) from Turkey and its taxonomic position among allied species
FIGURE 4. Leaf cross section of Allium istanbulense from living material of type locality.
FIGURE 1 in Phylogenetic position, taxonomy, distribution, and conservation status of the rare and poorly-known Noccaea rosularis, the generic type of Masmenia (Brassicaceae)
FIGURE 1. Distribution of Noccaea rosularis (Masmenia rosularis).
FIGURE 5 in A new genus and species of Parastenocarididae Chappuis, 1940 (Copepoda, Harpacticoida) from the Espinhaço Mountain Range (Brazil) with an unclear phylogenetic position within the Fontinalicaridinae Schminke, 2010
FIGURE 5- Tupinicaris rupestris gen. et sp. nov., male. Ventral (A) and lateral (B) views of P5.
FIGURE 1 in A new genus and species of Parastenocarididae Chappuis, 1940 (Copepoda, Harpacticoida) from the Espinhaço Mountain Range (Brazil) with an unclear phylogenetic position within the Fontinalicaridinae Schminke, 2010
FIGURE 1- Map indicating the type locality in the State Park of Rio Preto, Minas Gerais, Brazil.
FIGURE 7 in A new genus and species of Parastenocarididae Chappuis, 1940 (Copepoda, Harpacticoida) from the Espinhaço Mountain Range (Brazil) with an unclear phylogenetic position within the Fontinalicaridinae Schminke, 2010
FIGURE 7- Tupinicaris rupestris gen. et sp. nov., female. P1(A), P2 (B), P3 (C), P4 (D).
FIGURE 4 in A new genus and species of Parastenocarididae Chappuis, 1940 (Copepoda, Harpacticoida) from the Espinhaço Mountain Range (Brazil) with an unclear phylogenetic position within the Fontinalicaridinae Schminke, 2010
FIGURE 4- Tupinicaris rupestris gen. et sp. nov., male. P1(A), P2 (B), P3 (C), P4 (D).
Table 5 in Taxonomy and molecular phylogenetic position of new species and new records of Coelosphaeridae (Demospongiae: Poecilosclerida) from the Mexican Pacific
<p><b>Table 5.</b> Comparative data for the dimensions of the spicules (in µm) of <i>L. (W.) hawaiiana</i>. Shass length × width; head diameter are given for megascleres and total length for arcuate isochelae and sigmas. Values in parentheses are means</p><table><tbody><tr><th><b><i>L. (W.) hawaiiana</i> material examined</b></th><th><b>Tylotes</b></th><th><b>Oxeas</b></th><th><b>Arcuate isochelae</b></th><th><b>Sigmas</b></th></tr></tbody><tbody><tr><th>MBR-11506</th><td>200–(212.5)–225 × 2.5–(3)–5</td><td>185–(217.3)–250 × 2.5–(6.3)–7.5</td><td>10–(25.3)–35</td><td>10–(14.6)–25</td></tr><tr><th>LACM-1954</th><td>185–(200)–212.5 × 2.5–(3)–5</td><td>175–(191.8)–205 × 2.5–(6.8)–10</td><td>12.5–(21.6)–30</td><td>10–(11.1)–17.5</td></tr><tr><th>LEB-ICML-UNAM-147</th><td>165–(191.3)–215 × 2.5–(2.7)–5</td><td>185–(208.3)–225 × 2.5–(4.1)–10; 4.5–(6)–8</td><td>15–(25.7)–35</td><td>12.5–(14.6)–17</td></tr><tr><th>LEB-ICML-UNAM-396</th><td>200–(213.5)–235 × 2.5–(2.8)–3.9</td><td>128–(175)–226 × 2.5–(3.4)–5.2; 5–(6.3)–7.5</td><td>15.5–(21.8)–33</td><td>12.9–(17.5)–23</td></tr><tr><th>LEB-ICML-UNAM-1618</th><td>170–(195.6)–220 × 2.5–(4.2)–6.3; 5–(6.5)–7.5</td><td>190–(209.5)–220 × 2.5–(5.2)–7.5</td><td>17.5–(26.7)–35</td><td>I: 12.5–(14.1)–15 II: 32.5–49 (<i>N</i> = 2)</td></tr><tr><th>LEB-ICML-UNAM-1631</th><td>190–(207.7)–220 × 2.5–(3.05)–5</td><td>190–(208.75)–225 × 2.5–(4.375)–7.5</td><td>15–(20.5)–30</td><td>12.5–(14.09)–15</td></tr><tr><th>LEB-ICML-UNAM-1784</th><td>200–(213.5)–233.7 × 2.5–(2.8)–3.9</td><td>128–(166)–220 × 2.5–(3.4)–5.2</td><td>15.5–(21.8)–35</td><td>12.9–(17.5)–25</td></tr><tr><th>LEB-ICML-UNAM-1793</th><td>181–(198)–205 × 1.3–(3)–3.8</td><td>168–(191)–218 × 2.5–(5)–7.7</td><td>18–(25.5)–35</td><td>12.9–(15.8)–18 II: 32.5 (<i>N</i> = 1)</td></tr><tr><th>LEB-ICML-UNAM-1806</th><td>205–(208)–218 × 2.5–(2.8)–3.8</td><td>181–(191)–205 × 2.5–(4.1)–5</td><td>18–(19.1)–21.5</td><td>10–(12.5)–15</td></tr><tr><th>LEB-ICML-UNAM-1809</th><td>174–(198.5)–213 × 1.3–(2.5)–3.8</td><td>171–(190)–207 × 5–(6.7)–7.7</td><td>18–(26)–33.7</td><td>12.5–(15)–18</td></tr><tr><th>LEB-ICML-UNAM-1810</th><td>181–(195.5)–223 × 2.5–(3)–3.3</td><td>161–(175)–192 × 2.5–(5.3)–7.7</td><td>15–(25.3)–31</td><td>10–(12.9)–15</td></tr><tr><th>LEB-ICML-UNAM-1811</th><td>181–(201.1)–210 × 1.5–(4.2)–5</td><td>145–(188.9)–207.7 × 1.3–(4.4)–7.7</td><td>15.5–(27.5)–33.7</td><td>12.5–(15.5)–18</td></tr><tr><th>LEB-ICML-UNAM-1845</th><td>177.5–(201.8)–212.5 × 2.5–(3.4)–7.5</td><td>190–(207)–217.5 × 5–(7.5)–10</td><td>17.5–(27.5)–32.5</td><td>12.5–(14.1)–15 II: 30–(33)–36.3 (<i>N</i> = 4)</td></tr><tr><th>LEB-ICML-UNAM-1884</th><td>180–(198.8)–210 × 2.5–(3.6)–5</td><td>150–(191.2)–225 × 2.5–(5.6)–7.5</td><td>17.5–(27.6)–35</td><td>12.5–(14.3)–20</td></tr><tr><th>LEB-ICML-UNAM-1938</th></tr><tr><th>LEB-ICML-UNAM-2441</th><td>200–(213.5)–232.5 × 3.8–(4.9)–6.3; 5–(7)–8</td><td>155–(205.3)–230 × 6–(7.5)–10</td><td>17.5–(26.2)_37.5</td><td>I: 15–(15.8)–18 II: 37.5–40 (<i>N</i> = 2)</td></tr><tr><th>LEB-ICML-UNAM-2447</th><td>175–(187.8)–193 × 3–(3.6)–5; 3.8–(5.2)–7.5</td><td>132.5–(178.3)–210.5 × 2.5–(5.4)–8.8</td><td>15–(27.3)–35</td><td>I: 10–(12.8)–17.5 II: 35 (<i>N</i> = 1)</td></tr><tr><th>LEB-ICML-UNAM-3055</th><td>185–(195)–215 × 2.5–(4.3)–4; 5–(6.2)–7.5</td><td>165–(190)–212.5 × 2.5–(4.3)–5; (6.2)–7.5</td><td>15–(28.5)–37.5</td><td>I: 10–(14.4)–16.3 II: -</td></tr></tbody></table>
Table 3 in Taxonomy and molecular phylogenetic position of new species and new records of Coelosphaeridae (Demospongiae: Poecilosclerida) from the Mexican Pacific
<p><b>Table 3.</b> Comparative data for the dimensions of the spicules (in µm) of <b><i>Lissodendoryx (Anomodoryx) incrustans</i> sp. nov.</b>, shass length × width are given for megascleres and total length for arcuate isochelae and sigmas. Values in parentheses are means</p><table><tbody><tr><th><b>Material examined</b></th><th><b>Tylotes</b></th><th><b>Arcuate isochelae</b></th><th><b>Sigmas</b></th></tr><tr><th><b>Holotype</b></th></tr></tbody><tbody><tr><th>LEB-ICML-UNAM-449</th><td>150–(168.1)–200 × 2.5–(2.8)–5</td><td>12.5–(15.9)–20</td><td>15–(32.9)–40</td></tr><tr><th><b>Paratype</b></th></tr><tr><th>LEB-ICML-UNAM-1393</th><td>160–(213.3)–230 × 2.5–(2.5)–2.5</td><td>15–(16.9)–20</td><td>22.5–(35.4)–40</td></tr></tbody></table>
Table 4 in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)
<p><b>Table 4</b> Shell characters of <i>Lepidodesma aligera</i> and Lepidodesma languilati</p><table><tbody><tr><th>Characters</th><th><i>Lepidodesma aligera</i> (<i>n</i> =3)</th><th><i>Lepidodesma languilati</i> (<i>n</i> =6)</th></tr></tbody><tbody><tr><th>Length (mm)</th><td>161.38–175.22</td><td>192.25–207.67</td></tr><tr><th>Height (mm)</th><td>98.67–108.56</td><td>121.46–138.34</td></tr><tr><th>Width (mm)</th><td>75.33–81.78</td><td>83.18–88.35</td></tr><tr><th>Shell shape</th><td>Subtriangular</td><td>Subtriangular</td></tr><tr><th>Pseudocardinal teeth</th><td>Nearly absent</td><td>Nearly absent</td></tr><tr><th>Lateral teeth</th><td>2L, 1R</td><td>2L, 1R</td></tr><tr><th>Umbo position</th><td>1/4 of shell length; umbo higher than the dorsal margin</td><td>1/3 of shell length; umbo obviously higher than the dorsal margin</td></tr><tr><th>Umbo sculpture</th><td>Doubly looped or doubly noduled ridges</td><td>Doubly looped ridges</td></tr><tr><th>Umbo pocket</th><td>Deep, wide</td><td>Deep, wide</td></tr><tr><th>Surface sculpture</th><td>Ridges that follow the growth lines, two strong posterior dorsal ridges, and scattered nodules on the post-dorsal wing</td><td>Ridges that follow the growth lines and two strong posterior dorsal ridges</td></tr><tr><th>Nacre color</th><td>Orange, umbo pocket is pale green</td><td>Orange, umbo pocket is lilac</td></tr><tr><th>Dorsal margin</th><td>Anterior margin oval, dorsal margin nearly perpendicular</td><td>Anterior margin oval, with the dorsal margin curved</td></tr><tr><th></th><td>to the posterior margin, strongly curved upwards near the downwards posterior edge</td></tr><tr><th>Ventral margin</th><td>Slightly curve</td><td>Slightly curve</td></tr></tbody></table><p><i>L</i> left valve, <i>R</i> right valve</p>
Table 2 F in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)
<p><b>Table 2</b> F-type mtDNA sequences used for molecular analyses and corresponding GenBank numbers</p><table><tbody><tr><th><b>Family</b></th><th><b>Subfamily</b></th><th><b>Tribe</b></th><th><b>Taxa</b></th><th><b>Accession number</b></th></tr></tbody><tbody><tr><th>Unionidae</th><td>Unioninae</td><td>Nodulariini</td><td><i>Cuneopsis demangei</i></td><td>NC_066664</td><td>MZ571513</td></tr><tr><td><i>Cuneopsis heudei</i></td><td>NC_042471</td><td>MH919389</td></tr><tr><td><i>Cuneopsis celtiformis</i></td><td>MZ571520</td><td></td></tr><tr><td><i>Cuneopsis rufescens</i></td><td>NC_066663</td><td>MZ571512</td></tr><tr><td><i>Schistodesmus</i> sp. ‘ <i>Lamprotula gottschei</i> ’</td><td>NC_023806</td><td>KJ018924</td></tr><tr><td><i>Schistodesmus spinosus</i></td><td>NC_066662</td><td>MZ571511</td></tr><tr><td><i>Schistodesmus lampreyanus</i></td><td>NC_042470</td><td>MH919388</td></tr><tr><td><i>Tchangsinaia piscicula</i></td><td>NC_026306</td><td>KP273584</td></tr><tr><td><i>Nodularia breviconcha</i></td><td>MT955592</td><td></td></tr><tr><td><i>Nodularia douglasiae</i></td><td>NC_026111</td><td>KM657954</td></tr><tr><td><i>Pseudocuneopsis capitata</i></td><td>NC_042469</td><td>MH919387</td></tr><tr><td><i>Pseudocuneopsis sichuanensis</i></td><td>NC_066661</td><td>MZ571510</td></tr><tr><td>Unionini</td><td><i>Unio delphinus</i></td><td>NC_033854</td><td>KT326917</td></tr><tr><td><i>Unio pictorum</i></td><td>NC_015310</td><td>HM014130</td></tr><tr><td><i>Unio crassus</i></td><td>NC_033976</td><td>KY290446</td></tr><tr><td><i>Unio tumidus</i></td><td>KY021076</td><td></td></tr><tr><td><i>Unio elongatulus</i></td><td>MN594537</td><td></td></tr><tr><td><i>Unio mancus</i></td><td>MN594538</td><td></td></tr><tr><td>Aculamprotulini</td><td><i>Aculamprotula polysticta</i></td><td>MK728823</td><td></td></tr><tr><td><i>Aculamprotula scripta</i></td><td>NC_045529</td><td>KF991456</td></tr><tr><td><i>Aculamprotula coreana</i></td><td>NC_026035</td><td>JX050180</td></tr><tr><td><i>Aculamprotula tientsinensis</i></td><td>NC_029210</td><td></td></tr><tr><td><i>Aculamprotula tortuosa</i></td><td>NC_021404</td><td>KC109779</td></tr><tr><td>Anodontini</td><td><i>Alasmidonta varicosa</i></td><td>NC_038155</td><td>MG938673</td></tr><tr><td><i>Lasmigona complanata</i></td><td>OM736811</td><td></td></tr><tr><td><i>Platynaias compressa</i></td><td>HM856638</td><td></td></tr><tr><td><i>Prolasmidonta heterodon</i></td><td>MG905826</td><td></td></tr><tr><td><i>Utterbackia imbecillis</i></td><td>NC_015479</td><td>HM856637</td></tr><tr><td><i>Utterbackia peninsularis</i></td><td>HM856636</td><td></td></tr><tr><td><i>Pyganodon grandis</i></td><td>NC_013661</td><td>FJ809754</td></tr><tr><td><i>Anodonta anatina</i></td><td>NC_022803</td><td>KF030964</td></tr><tr><td><i>Anodonta exulcerata</i></td><td>MN594533</td><td></td></tr><tr><td><i>Anodonta nuttalliana</i></td><td>MN594534</td><td></td></tr><tr><td><i>Anodonta cygnea</i></td><td>NC_036488</td><td>MG385135</td></tr><tr><td><i>Pseudanodonta complanata</i></td><td>MN594535</td><td></td></tr><tr><td>Cristariini</td><td><i>Anemina arcaeformis</i></td><td>NC_026674</td><td>KF667530</td></tr><tr><td><i>Anemina euscaphys</i></td><td>NC_026792</td><td>KP187851</td></tr><tr><td><i>Sinanodonta tumens</i></td><td>LC592406</td><td></td></tr><tr><td><i>Sinanodonta lucida</i></td><td>NC_026673</td><td>KF667529</td></tr><tr><td><i>Sinanodonta woodiana</i></td><td>HQ283346</td><td></td></tr><tr><td><i>Beringiana fukuharai</i></td><td>LC592410</td><td></td></tr><tr><td><i>Cristaria plicata</i></td><td>KM233451</td><td></td></tr><tr><td>Lanceolariini</td><td><i>Acuticosta chinensis</i></td><td>NC_042472</td><td>MH919390</td></tr><tr><td><i>Lanceolaria lanceolata</i></td><td>NC_023955</td><td>KJ144818</td></tr><tr><td><i>Lanceolaria gladiola</i></td><td>KY067441</td><td></td></tr><tr><td><i>Lanceolaria grayii</i></td><td>NC_026686</td><td>KJ495725</td></tr><tr><td>Lepidodesmini</td><td><i>Lepidodesma aligera</i> <i>a</i></td><td>OP859025</td><td></td></tr><tr><td><i>Lepidodesma languilati</i> <i>a</i></td><td>OQ910483</td><td></td></tr><tr><th></th><td>Parreysiinae</td><td>Lamellidentini</td><td><i>Lamellidens marginalis</i></td><td>NC_062877</td><td>MT230549</td></tr><tr><th></th><td>Gonideinae</td><td>Gonideini</td><td><i>Parvasolenaia rivularis</i></td><td>NC_039839</td><td>KX966393</td></tr><tr><th></th><td><i>Ptychorhynchus pfisteri</i></td><td>KY067440</td><td></td></tr><tr><th></th><td><i>Sinosolenaia carinata</i></td><td>NC_023250</td><td>KC848654</td></tr><tr><th></th><td><i>Sinosolenaia oleivora</i></td><td>NC_022701</td><td>KF296320</td></tr><tr><th></th><td><i>Sinosolenaia iridinea</i></td><td>MT477834</td><td></td></tr><tr><th></th><td><i>Microcondylaea bonellii</i></td><td>NC_044111</td><td>MK994772</td></tr><tr><th></th><td>Lamprotulini</td><td><i>Lamprotula caveata</i></td><td>NC_030336</td><td>KX060991</td></tr><tr><th></th><td><i>Lamprotula leaii</i></td><td>NC_023346</td><td>JQ691662</td></tr><tr><th></th><td><i>Lamprotula cornuumlunae</i></td><td>MK728822</td><td></td></tr><tr><th></th><td><i>Potomida littoralis</i></td><td>NC_030073</td><td>KT247374</td></tr><tr><th></th><td><i>Pronodularia japanensis</i></td><td>AB055625</td><td></td></tr><tr><th></th><td>Pseudodontini</td><td><i>Monodontina vondembuschiana</i></td><td>NC_044112</td><td>MK994774</td></tr><tr><th></th><td><i>Pilsbryoconcha exilis</i></td><td>NC_044124</td><td>MK994776</td></tr><tr><th></th><td>Contradentini</td><td><i>Lens contradens</i></td><td>MW242812</td><td></td></tr><tr><th></th><td><i>Physunio superbus</i></td><td>MW242814</td><td></td></tr><tr><th></th><td>Rectidentini</td><td><i>Hyriopsis bialata</i></td><td>MW242816</td><td></td></tr><tr><th></th><td><i>Rectidens sumatrensis</i></td><td>MW242818</td><td></td></tr><tr><th></th><td>Chamberlainiini</td><td><i>Sinohyriopsis cumingii</i></td><td>NC_011763</td><td>FJ529186</td></tr><tr><th></th><td><i>Sinohyriopsis schlegelii</i></td><td>NC_015110</td><td>HQ641406</td></tr><tr><th></th><td><i>Chamberlainia hainesiana</i></td><td>NC_044110</td><td>MK994770</td></tr><tr><th></th><td>Ambleminae</td><td>Lampsilini</td><td><i>Lampsilis powellii</i></td><td>NC_037720</td><td>MF326971</td></tr><tr><th></th><td><i>Lampsilis siliquoidea</i></td><td>NC_037721</td><td>MF326973</td></tr><tr><th></th><td><i>Venustaconcha ellipsiformis</i></td><td>FJ809753</td><td></td></tr><tr><th></th><td><i>Lampsilis cardium</i></td><td>BK010478</td><td></td></tr><tr><th></th><td><i>Lampsilis cariosa</i></td><td>OM736866</td><td></td></tr><tr><th></th><td><i>Lampsilis ornata</i></td><td>NC_005335</td><td>AY365193</td></tr><tr><th></th><td><i>Leaunio lienosus</i></td><td>BK010479</td><td></td></tr><tr><th></th><td><i>Potamilus alatus</i></td><td>KU559011</td><td></td></tr><tr><th></th><td><i>Potamilus streckersoni</i></td><td>ON855351</td><td></td></tr><tr><th></th><td><i>Potamilus leptodon</i></td><td>NC_028522</td><td>KT723012</td></tr><tr><th></th><td><i>Toxolasma parvum</i></td><td>NC_015483</td><td>HM856639</td></tr><tr><th></th><td>Popenaiadini</td><td><i>Popenaias popeii</i></td><td>NC_050058</td><td>MT648776</td></tr><tr><th></th><td>Amblemini</td><td><i>Amblema plicata</i></td><td>NC_050056</td><td>MT648774</td></tr><tr><th></th><td>Pleurobemini</td><td><i>Elliptio complanata</i></td><td>BK010477</td><td></td></tr><tr><th></th><td><i>Pleurobema oviforme</i></td><td>NC_050057</td><td>MT648775</td></tr><tr><th></th><td>Quadrulini</td><td><i>Quadrula quadrula</i></td><td>NC_013658</td><td>FJ809750</td></tr><tr><th></th><td><i>Uniomerus tetralasmus</i></td><td>BK010480</td><td></td></tr><tr><th>Margaritiferidae</th><td>Margaritiferinae</td><td><i>Margaritifera dahurica</i></td><td>NC_023942</td><td>KF514426</td></tr><tr><td><i>Margaritifera falcata</i></td><td>NC_015476</td><td>HM856634</td></tr><tr><td><i>Margaritifera margaritifera</i></td><td>KY996745</td><td></td></tr><tr><td><i>Pseudunio marocanus</i></td><td>NC_034911</td><td>KY131953</td></tr><tr><td><i>Cumberlandia monodonta</i></td><td>NC_034846</td><td>KU873123</td></tr><tr><td>Gibbosulinae</td><td><i>Gibbosula crassa</i></td><td>NC_037942</td><td>MH319826</td></tr><tr><td></td><td><i>Gibbosula rochechouartii</i></td><td>KX378172</td><td></td></tr><tr><th>Hyriidae</th><td>Hyriinae</td><td><i>Echyridella menziesii</i></td><td>NC_034845</td><td>KU873121</td></tr><tr><th>Iridinidae</th><td>Iridininae</td><td><i>Mutela dubia</i></td><td>NC_034844</td><td>KU873120</td></tr><tr><th>Mycetopodidae</th><td>Anodontitinae</td><td><i>Anodontites trapesialis</i></td><td>KU873119</td><td></td></tr><tr><th>Trigoniidae</th><td><i>Neotrigonia margaritacea</i></td><td>NC_034843</td><td>KU873118</td></tr></tbody></table><p><sup>aThe</sup> sequence from this study</p>
Dataset for the paper "Efficient sentence processing significantly affects the position of objects in Russian"
<p>Dataset and the scripts for the paper "Efficient sentence processing significantly affects the position of objects in Russian"</p>
Linked collectors and determiners for: The systematic position of Pamera noctuabunda Bergroth, 1907 (Hemiptera: Heteroptera: Rhyparochromidae), with a revised key to the species of Stalaria Harrington, 1980.
Natural history specimen data linked to collectors and determiners held within, "The systematic position of Pamera noctuabunda Bergroth, 1907 (Hemiptera: Heteroptera: Rhyparochromidae), with a revised key to the species of Stalaria Harrington, 1980". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/cb23c8ce-d093-4dfc-9d46-8f20ee18a6e8">https://bionomia.net/dataset/cb23c8ce-d093-4dfc-9d46-8f20ee18a6e8</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/cb23c8ce-d093-4dfc-9d46-8f20ee18a6e8">https://gbif.org/dataset/cb23c8ce-d093-4dfc-9d46-8f20ee18a6e8</a>. Formatted as a Frictionless Data package.
Full-waveform inversion reveals diverse origins of lower mantle positive wave speed anomalies
Open the record for dataset details and reuse information.
Energy distribution of negatively and positively charged ions in a magnetron sputtering discharge with a tungsten cathode and a positively biased anode in an argon/oxygen gas mixture.
<p>The energy distribution of negatively and positively charged ions in a magnetron discharge with a positively biased anode is investigated. A tungsten cathode operated in an argon/oxygen gas mixture is employed. The magnetron is operated either in direct current (DCMS) or in high power impulse magnetron sputtering (HiPIMS) mode.</p>
Data set and control code for "Force-Sensor-Free Implementation of a Hybrid Position–Force Control for Overconstrained Cable-Driven Parallel Robots"
<p>See the attached readme file</p>
Data from: The experimental evolution of herbicide-resistance in Chlamydomonas reinhardtii results in a positive correlation between fitness in the presence and absence of herbicides
Pleiotropic fitness trade-offs will be key determinants of the evolutionary dynamics of selection for pesticide resistance. However, for herbicide resistance, empirical support for a fitness cost of resistance is mixed, and it is therefore also questionable what further ecological trade-offs can be assumed to apply to herbicide resistance. Here, we test the existence of trade-offs by experimentally evolving herbicide resistance in Chlamydomonas reinhardtii. Although fitness costs are detected for all herbicides, we find that, counterintuitively, the most resistant populations also have the lowest fitness costs as measured by growth rate in the ancestral environment. Furthermore, after controlling for differences in the evolutionary dynamics of resistance to different herbicides, we also detect significant positive correlations between resistance, fitness in the ancestral environment and cross-resistance to other herbicides. We attribute this to the highest levels of nontarget-site resistance being achieved by fixing mutations that more broadly affect cellular physiology, which results in both more cross-resistance and less overall antagonistic pleiotropy on maximum growth rate. Consequently, the lack of classical ecological trade-offs could present a major challenge for herbicide resistance management.
Data from: The systematic position of the stonefly †culonga Sinitshenkova, 2011 (Plecoptera: Leuctrida) reassessed using Reflectance Transforming Imaging and cladistic analysis
The phylogenetic position of the insect species †culonga Sinitshenkova, 2011, recovered from the Khasurty locality (Transbaikalia, Russia; Early Cretaceous), is re-investigated. This fossil needle stonefly has been considered an Exeleuctrida nec Mioleuctrida & Eleuctrida based on the organization of the hind wing venation opposite the arculus. We reconsidered this interpretation based on a direct observation, complemented by a Reflectance Transforming Imaging file. Our investigation indicates that the species displays the defining character state of Eleuctrida while it lacks the defining character state of Mioleuctrida. Due to inconsistencies in the character state combination displayed by the species, we carried out a cladistics analysis. The species †culonga is recovered as an Eleuctrida nec Mioleuctrida, and therefore represents a suitable calibration point for a node more recent than previously assumed, and incidentally demonstrates that Mioleuctrida belongs to Eleuctrida.
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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.