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Fig. 5 in A new species of mesonychian mammal from the lower Eocene of Mongolia and its phylogenetic relationships
Fig. 5. Dissacus zanabazari sp. nov., holotype, MAE−BU−97−13786, Tsagaan Khushuu, Gobi Desert, Mongolia, early Eocene. Left scapula shown in ventral (A) and lateral (B) views C. Stereopair of left manus, in anterior view. Abbreviations: ce, centrale; Mc, metacarpal; mg, magnum; td, trapezoid.
Fig. 6 in A new species of mesonychian mammal from the lower Eocene of Mongolia and its phylogenetic relationships
Fig. 6. Dissacus zanabazari sp. nov., holotype, MAE−BU−97−13786, Tsagaan Khushuu, Gobi Desert, Mongolia, early Eocene. A. Left radius and ulna in medial view. B. Right humerus in anterior view.
Fig. 7. A in A new species of mesonychian mammal from the lower Eocene of Mongolia and its phylogenetic relationships
Fig. 7. A. Medial view of the left manus of Dissacus zanabazari sp. nov., holotype, MAE−BU−97−13786, Tsagaan Khushuu, Gobi Desert, Mongolia, early Eocene. B. Explanatory drawing of the same.
Fig. 12 in A new species of mesonychian mammal from the lower Eocene of Mongolia and its phylogenetic relationships
Fig. 12. Phylogenetic position of Dissacus zanabazari as depicted in a strict consensus of 8 most parsimonious trees, each 220 steps in length. Bremer support values are placed below and to the left of each node. Abbreviation: H, Hapalodectidae.
Fig. 10 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 10. Line drawings of Russula purpureomarginalis F.Li & Y.Song sp. nov., holotype (SERC2211). A. Basidia. B. Cheilocystidia. C. Pleurocystidia. D. Pileocystidia near pileus margin. E. Hyphal terminations near pileus margin. Scale bar = 10 µm.
Fig. 8 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 8. Line drawings of Russula minirosea Y.Song sp. nov., holotype (SERC2205). A. Basidia. B. Cheilocystidia. C. Pleurocystidia. D. Pileocystidia near pileus margin. E. Hyphal terminations near pileus margin. Scale bar = 10 µm.
Fig. 9. Russula purpureomarginalis F.Li & Y in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 9. Russula purpureomarginalis F.Li & Y.Song sp. nov., holotype (SERC2211). A–C. Fruiting bodies. D–E. Basidia. F. Pileocystidia near pileus margin. G. Basidiospores in Melzer's reagent showing the amyloid ornamentations. Scale bars: A–C = 1 cm; D–G = 10 µm.
Fig. 7. Russula minirosea Y in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 7. Russula minirosea Y.Song sp. nov. A–H. Fruiting bodies. A, D–E. Holotype (SERC2205) B. SERC2206. C. SERC2207. F–G. SERC2208. H. SERC2302. I. Basidiospores in Melzer's reagent showing the amyloid ornamentations, holotype (SERC2205). Scale bars: A–H = 1 cm; I = 10 µm.
Fig. 5. Russula micangshanensis Y in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 5. Russula micangshanensis Y.Song sp. nov. A–H. Fruiting bodies. A, H. Holotype (SERC2201). B–C. SERC2202. D. SERC2303. E. SERC2304. F. SERC2305. G. SERC2307. I. Basidiospores in Melzer's reagent showing the amyloid ornamentations (SERC2201). Scale bars: A–H = 1 cm; I = 10 µm.
Fig. 6 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 6. Line drawings of Russula micangshanensis Y.Song sp. nov., holotype (SERC2201). A. Basidia. B. Cheilocystidia. C. Pleurocystidia. D. Hyphal terminations near pileus margin. Scale bar = 10 µm.
Fig. 11 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 11. Photograph of basidiospores under scanning electron microscope. A–B. Russula micangshanensis Y.Song sp. nov., holotype (SERC2201). C–D. R. minirosea Y.Song sp. nov., holotype (SERC2201). E–F. R. griseorosea Y.Song sp. nov., holotype (SERC2209). G–H. R. purpureomarginalis F.Li & Y.Song sp. nov., holotype (SERC2211). Scale bars = 1 µm.
Fig. 4 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 4. Line drawings of Russula griseorosea Y.Song sp. nov., holotype (SERC2209). A. Basidia. B. Cheilocystidia. C. Pleurocystidia. D. Pileocystidia near pileus margin. E. Hyphal terminations near pileus margin. Scale bar = 10 µm.
Fig. 3. Russula griseorosea Y in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 3. Russula griseorosea Y.Song sp. nov., holotype (SERC2209). A–C. Fruiting bodies. D–E. Basidiospores in Melzer's reagent showing the amyloid ornamentations. F. Pileocystidia near pileus margin. G–H. Basidia and basidiole in the hymenium. Scale bars: A–C = 1 cm; D–H = 10 µm.
Fig. 2 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 2. Maximum likelihood tree of subgen. Russula crown clade based on 3-locus (nLSU-tef1-rpb2) combined sequences, bootstrap (BS) values higher than 50% and posterior probability (PP) values higher than 0.9 are presented around nodes. Newly generated sequences are shown in bold and four new species are highlighted in green.
Fig. 1 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
Fig. 1. Maximum likelihood tree of subg. Russula crown clade based on ITS sequences, bootstrap (BS) values higher than 50% and posterior probability (PP) values higher than 0.9 are displayed around nodes. Newly generated sequences are shown in bold and clades with four new species are highlighted in green.
Species introductions cause phylogenetically structured successional pathways in natural wood-inhabiting fungal communities
<p>These files include the data and the scripts for reproducing the results presented in the manuscript "Species introductions cause phylogenetically structured successional pathways in natural wood-inhabiting fungal communities".</p> <p>Description of the files can be found from the README.docx file.</p>
Table 2 in Phylogenetic and morphological evidence for four new species of Russula (Russulaceae, Basidiomycota) from northwestern China
<p><b>Table 2</b> (continued on next page). Sequences used in the multi-locus phylogenetic analysis. Newly generated sequences are shown in <b>bold</b>.</p><table><tbody><tr><th><b>Taxon</b></th><th><b>Voucher specimen</b></th><th><b>Location</b></th><th>Accession <b>number</b></th><th><b>Reference</b></th></tr><tr><th>nucLSU</th><th><i>rpb2</i></th><th><i>tef1</i></th></tr></tbody><tbody><tr><th><i>R.</i> aff. <i>fucosa</i></th><td>BB 06.596</td><td>Canada</td><td>KU237457</td><td>KU237743</td><td>KU237892</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R.</i> aff. <i>xerampelina</i></th><td>DM fl07-14</td><td>USA</td><td>KU237576</td><td>KU237862</td><td>KU238004</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. carpini</i></th><td>BB 07.262</td><td>Slovakia</td><td>KU237543</td><td>KU237829</td><td>KU237973</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R.</i> cf. <i>appalachiensis</i></th><td>BPL250</td><td>USA</td><td>–</td><td>KT933893</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R.</i> cf. <i>aurantioflammans</i></th><td>BB 06.603</td><td>Canada</td><td>KU237488</td><td>KU237774</td><td>KU237917</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R.</i> cf. <i>brunneoviolacea</i></th><td>BB 06.606</td><td>Canada</td><td>KU237516</td><td>KU237802</td><td>KU237946</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R.</i> cf. <i>decipiens</i></th><td>BPL266 (TENN)</td><td>USA</td><td>KT933827</td><td>KT933899</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R.</i> cf. <i>decipiens</i></th><td>BB 06.521</td><td>Mexico</td><td>KU237482</td><td>KU237768</td><td>KU237911</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R.</i> cf. <i>katarinae</i></th><td>BB 06.617</td><td>Canada</td><td>KU237460</td><td>KU237746</td><td>KU237895</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th>R. cf. <i>odorata</i></th><td>BB 07.219</td><td>Slovakia</td><td>KU237517</td><td>KU237803</td><td>KU237947</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R.</i> cf. <i>rugulosa</i></th><td>BPL237 (TENN)</td><td>USA</td><td>KT933814</td><td>KT933885</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R.</i> cf. <i>sejuncta</i></th><td>BB 08.143</td><td>Madagascar</td><td>KU237547</td><td>KU237833</td><td>–</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R.</i> cf. <i>versicolor</i></th><td>FH12259 (GENT)</td><td>Germany</td><td>KT933873</td><td>KT933944</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R.</i> cf. <i>vinosobrunea</i></th><td>BB 07.231</td><td>Slovakia</td><td>KU237525</td><td>KU237811</td><td>KU237955</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. changbaiensis</i></th><td>HMAS262355</td><td>China</td><td>KX441304</td><td>KX442045</td><td>MF893389</td><td>–</td></tr><tr><th><i>R. citrinolutea</i></th><td>BB 06.611</td><td>Canada</td><td>KU237459</td><td>KU237745</td><td>KU237894</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. coronaspora</i></th><td>GDGM79711 (holotype)</td><td>China</td><td>MN839580</td><td>MT085657</td><td>MT085600</td><td>Song <i>et al.</i> 2021</td></tr><tr><th><i>R. cremeirosea</i></th><td>BPL289 (TENN)</td><td>USA</td><td>KT933844</td><td>KT933915</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R. curtipes</i></th><td>FH12206 (GENT)</td><td>Germany</td><td>KT933856</td><td>KT933927</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R. decipiens</i></th><td>BB 07.178</td><td>Slovakia</td><td>KU237569</td><td>KU237855</td><td>KU237997</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. flavobrunnescens</i></th><td>AK5024 (holotype)</td><td>Mexico</td><td>–</td><td>MN380530</td><td>–</td><td>Adamčík <i>et al.</i> 2019</td></tr><tr><th><i>R. font-queri</i></th><td>FH12223 (GENT)</td><td>Germany</td><td>KT933864</td><td>KT933935</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R. griseorosea</i> <b>sp</b>. <b>nov</b>.</th><td><b>SERC2209 (holotype)</b></td><td><b>China</b></td><td><b>OP828718</b></td><td><b>OP831169</b></td><td><b>OP857222</b></td><td><b>Present study</b></td></tr><tr><th><i>R. laricina</i></th><td>BB 08.681</td><td>Italy</td><td>KU237560</td><td>KU237846</td><td>KU237991</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. madrensis</i></th><td>AK3422 (holotype)</td><td>Mexico</td><td>–</td><td>MN380520</td><td>–</td><td>Adamčík <i>et al.</i> 2019</td></tr><tr><th><i>R. melliolens</i></th><td>BB 07.194</td><td>Slovakia</td><td>KU237545</td><td>KU237831</td><td>KU237975</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. micangshanensis</i> <b>sp</b>. <b>nov</b>.</th><td><b>SERC2201 (holotype)</b></td><td><b>China</b></td><td><b>OP828723</b></td><td><b>OP831174</b></td><td><b>–</b></td><td><b>Present study</b></td></tr><tr><th><i>R. minirosea</i> <b>sp</b>. <b>nov</b>.</th><td><b>SERC2205 (holotype)</b></td><td><b>China</b></td><td><b>OP828720</b></td><td><b>OP831171</b></td><td><b>OP857224</b></td><td><b>Present study</b></td></tr><tr><th><i>R. minirosea</i> <b>sp</b>. <b>nov</b>.</th><td><b>SERC2206</b></td><td><b>China</b></td><td><b>OP828719</b></td><td><b>OP831170</b></td><td><b>OP857223</b></td><td><b>Present study</b></td></tr><tr><th><i>R. minirosea</i> <b>sp</b>. <b>nov</b>.</th><td><b>SERC2207</b></td><td><b>China</b></td><td><b>OP828721</b></td><td><b>OP831172</b></td><td><b>OP857225</b></td><td><b>Present study</b></td></tr><tr><th><i>R. minirosea</i> <b>sp</b>. <b>nov</b>.</th><td><b>SERC2208</b></td><td><b>China</b></td><td><b>OP828722</b></td><td><b>OP831173</b></td><td><b>OP857226</b></td><td><b>Present study</b></td></tr><tr><th><i>R. nauseosa</i></th><td>BB 07.285</td><td>Slovakia</td><td>KU237572</td><td>KU237858</td><td>KU238000</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. nauseosa</i></th><td>FH12173 (GENT)</td><td>Germany</td><td>KT933846</td><td>KT933917</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R. nitida</i></th><td>FH12218 (GENT)</td><td>Germany</td><td>KT933862</td><td>KT933933</td><td>–</td><td>Looney <i>et al.</i> 2016</td></tr><tr><th><i>R. obscurosordida</i></th><td>BB 06.564</td><td>Canada</td><td>KU237575</td><td>KU237861</td><td>KU238003</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. odorata</i></th><td>BB 07.186</td><td>Slovakia</td><td>KU237518</td><td>KU237804</td><td>KU237948</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. olivacea</i></th><td>BB 07.223</td><td>Slovakia</td><td>KU237492</td><td>KU237778</td><td>KU237921</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. minor</i></th><td>GDGM79686 (holotype)</td><td>China</td><td>MK881964</td><td>MK880691</td><td>MT085599</td><td>Song <i>et al.</i> 2021</td></tr><tr><th><i>R. minor</i></th><td>GDGM79689</td><td>China</td><td>MN839576</td><td>MT085653</td><td>MT085624</td><td>Song <i>et al.</i> 2021</td></tr><tr><th><i>R. puellaris</i></th><td>BB 07.311</td><td>Slovakia</td><td>KU237515</td><td>KU237801</td><td>KU237945</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. purpureomarginalis</i> <b>sp</b>. <b>nov</b>.</th><td><b>SERC2211 (holotype)</b></td><td><b>China</b></td><td><b>OP828727</b></td><td><b>OP831178</b></td><td><b>OP857230</b></td><td><b>Present study</b></td></tr><tr><th><i>R. rugulosa</i></th><td>BPL654</td><td>USA</td><td>–</td><td>KY701373</td><td>KY701415</td><td>Looney <i>et al.</i> 2020</td></tr><tr><th><i>R. sinoparva</i></th><td>BJTC C540</td><td>China</td><td>OP133234</td><td>OP156829</td><td>OP156839</td><td>Zhou <i>et al.</i> 2022</td></tr><tr><th><i>R. solaris</i></th><td>BB 07.282</td><td>Slovakia</td><td>KU237549</td><td>KU237835</td><td>KU237978</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. tlaxcalae</i></th><td>BB 06.542</td><td>Mexico</td><td>KU237463</td><td>KU237749</td><td>KU237897</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. subversatilis</i></th><td>BJTC C653 (holotype)</td><td>China</td><td>OP133238</td><td>OP156832</td><td>OP156844</td><td>Zhou <i>et al.</i> 2022</td></tr><tr><th><i>R. versicolor</i></th><td>BB 07.288</td><td>Slovakia</td><td>KU237573</td><td>KU237859</td><td>KU238001</td><td>Buyck <i>et al.</i> 2018</td></tr><tr><th><i>R. yanshanensis</i></th><td>BJTC Z1305</td><td>China</td><td>OP133243</td><td>OP156834</td><td>OP156848</td><td>Zhou <i>et al.</i> 2022</td></tr><tr><th>Outgroup</th></tr><tr><th><i>R. glutinosa</i></th><td>Roody WRWV 04.1154 (holotype)</td><td>USA</td><td>MN315511</td><td>MN326798</td><td>MN326799</td><td>Buyck <i>et al.</i> 2020</td></tr><tr><th><i>R. glutinosoides</i></th><td>HKAS106678 (holotype)</td><td>China</td><td>MN428827</td><td>–</td><td>–</td><td>Buyck <i>et al.</i> 2020</td></tr></tbody></table>
Linked collectors and determiners for: Phylogenetic analysis of the Taeniothrips genus-group, with revision of the species of Ctenothrips and Vulgatothrips (Thysanoptera, Thripinae).
Natural history specimen data linked to collectors and determiners held within, "Phylogenetic analysis of the Taeniothrips genus-group, with revision of the species of Ctenothrips and Vulgatothrips (Thysanoptera, Thripinae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/68aa6965-5a25-41ac-80ac-9a899e24bc94">https://bionomia.net/dataset/68aa6965-5a25-41ac-80ac-9a899e24bc94</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/68aa6965-5a25-41ac-80ac-9a899e24bc94">https://gbif.org/dataset/68aa6965-5a25-41ac-80ac-9a899e24bc94</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Phylogenetic systematics, ecology, and conservation of marsupial frogs (Anura: Hemiphractidae) from the Andes of southern Ecuador, with descriptions of four new biphasic species.
Natural history specimen data linked to collectors and determiners held within, "Phylogenetic systematics, ecology, and conservation of marsupial frogs (Anura: Hemiphractidae) from the Andes of southern Ecuador, with descriptions of four new biphasic species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/da18d6cf-db48-4fc6-b74d-2e763b6bf888">https://bionomia.net/dataset/da18d6cf-db48-4fc6-b74d-2e763b6bf888</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/da18d6cf-db48-4fc6-b74d-2e763b6bf888">https://gbif.org/dataset/da18d6cf-db48-4fc6-b74d-2e763b6bf888</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Description of two new species and phylogenetic reassessment of Perelleschus O'Brien & Wibmer, 1986 (Coleoptera: Curculionidae), with a complete taxonomic concept history of Perelleschus sec. Franz & Cardona-Duque, 2013.
Natural history specimen data linked to collectors and determiners held within, "Description of two new species and phylogenetic reassessment of Perelleschus O'Brien & Wibmer, 1986 (Coleoptera: Curculionidae), with a complete taxonomic concept history of Perelleschus sec. Franz & Cardona-Duque, 2013". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/af97dd93-ad80-4dcf-af96-c67a1cc0901e">https://bionomia.net/dataset/af97dd93-ad80-4dcf-af96-c67a1cc0901e</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/af97dd93-ad80-4dcf-af96-c67a1cc0901e">https://gbif.org/dataset/af97dd93-ad80-4dcf-af96-c67a1cc0901e</a>. Formatted as a Frictionless Data package.
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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.