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FIG. 11 in A world revisionary study of the genus Groutiella Steere (Orthotrichaceae, Bryopsida)
FIG. 11. — Groutiella tomentosa (Hornsch.) Wijk & Margad.: A, plant; B-G, leaves; H, apical leaf cells; I, median marginal leaf cells; J, basal leaf cells; K, perichaetial bract; L, capsule; M, calyptra; N, portion of peristome; O, phaneropore; P, spores. A, K-P from Larsen et al. 2362 (MO); B, C from de Robillard s.n., lectotype of G. laxotorquata (Müll. Hal. ex Besch.) Wijk & Margad.; D-G from Allen 25041 (MO); H-J from Sellow s.n., lectotype of G. tomentosa, H. Scale bar: A, 1.2 cm; B-J, 90 µm; K, 0.9 mm; L, M, 3 mm; N-P, 130 µm. Credits: Yu N.-N. & Guo M. S.
FIG. 3 in A world revisionary study of the genus Groutiella Steere (Orthotrichaceae, Bryopsida)
FIG. 3. — Capsules, peristome and spores of Groutiella Steere: A, G. apiculata (Hook.) H.A. Crum & Steere; B, D, E, G. husnotii (Schimp. ex Besch.) H.A. Crum & Steere; C, G. tumidula (Mitt.) Vitt.; F, H, G. wagneriana (Müll. Hal.) H.A. Crum & Steere; G, G. obtusa (Mitt.) Florsch. A from Allen 15136 (MO); B, D, E from Steere 7180 (MO); C from Vital 2319 (MO); F, H from Pringle 10560 (MO); G from Liesner 16772A (NSW). Scale bars: A-C, 3 mm; D, 250 µm; E, 25 µm; F, G, 5 µm; H, 2.5 µm.
TABLE 2 in Studies in Austral Bryaceae (Bryopsida). IV. New records from the Falkland Islands (Islas Malvinas), with a phytogeographic analysis of the family
<p>TABLE 2. — Sorenson’s coefficient of similarity among six regions in the southern hemisphere for the moss family Bryaceae. The larger the percent similarity the more similar floras are to each other.Abbreviations: <b>FI</b>, Falkland Islands; <b>NZ</b>, South Island and offshore islands of New Zealand with some extensions to the North Island; <b>SA</b>, South Africa; <b>SAM</b>, southern South America; <b>SI</b>, subantarctic islands; <b>TAS</b>, Tasmania, with extensions to southeast Australia.</p><table><tbody><tr><th></th><th><b>SAM</b></th><th><b>FI</b></th><th><b>NZ</b></th><th><b>TAS</b></th><th><b>SA</b></th><th><b>SI</b></th></tr></tbody><tbody><tr><th>SAM</th><td>100</td><td>77.4</td><td>64</td><td>51</td><td>41</td><td>54.4</td></tr><tr><th>FI</th><td>–</td><td>100</td><td>75</td><td>58.7</td><td>38.3</td><td>54</td></tr><tr><th>NZ</th><td>–</td><td>–</td><td>100</td><td>92.5</td><td>40.8</td><td>75</td></tr><tr><th>TAS</th><td>–</td><td>–</td><td>–</td><td>100</td><td>55.6</td><td>68.1</td></tr><tr><th>SA</th><td>–</td><td>–</td><td>–</td><td>–</td><td>100</td><td>38.8</td></tr><tr><th>SI</th><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>100</td></tr></tbody></table>
APPENDIX 1 in Studies in Austral Bryaceae (Bryopsida). IV. New records from the Falkland Islands (Islas Malvinas), with a phytogeographic analysis of the family
<p>APPENDIX 1. — List of Bryaceae species from the southern hemisphere used in the study. Although <i>Bryum chrysoneuron</i> Müll.Hal. is reported from the subantarctic Macquarie Island it is likely misidentified (R. Seppelt, pers. comm. 2021). Its removal from the analyses would not affect the results. <i>Bryum gilliesii</i> Hook. and <i>B. platyphyllum</i> Müll.Hal. are placed within <i>Plagiobryoides</i> J.R.Spence as they are likely members of that genus. <i>Bryum lamprocarpum</i> Müll.Hal. is placed within <i>Plagiobryum</i> Lindb. as it may be a member of that genus. Neither combination was made.</p><table><tbody><tr><th><b>Genus</b></th><th>Species</th><th><b>Tierra del</b> <b>Fuego/</b> <b>S. Patagonia</b></th><th><b>Falklands</b></th><th><b>New Zealand</b></th><th><b>Tasmania</b></th><th>South Africa</th><th><b>Sub</b> Islands</th><th><b>Antarctica</b></th></tr></tbody><tbody><tr><th><i>Anomobryum</i></th><td><i>A. drakensbergense</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td><td>–</td></tr><tr><td><i>A. julaceum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td></tr><tr><th><i>Brachymenium</i></th><td><i>B. magellanicum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th><i>Bryum</i></th><td><i>B. argenteum</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td></tr><tr><td><i>B. badium</i></td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. barnesii</i></td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. caespiticium</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td></tr><tr><td><i>B. dichotomum</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td></tr><tr><td><i>B. funkii</i></td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. harriotii</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>B. microimbricatum</i></td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. miserum</i></td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. pabstianum</i></td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. rhizoblastum</i></td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. sabuletorum</i></td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>B. sauteri</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>1</td><td>–</td></tr><tr><th><i>Imbribryum</i></th><td><i>I. alpinum</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td><td>–</td></tr><tr><td><i>I. australe</i></td><td>1</td><td>–</td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>Bryum chrysoneuron</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>I. clavatum</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>I. crassinervium</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>I. laevigatum</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>I. subapiculatum</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td></tr><tr><td><i>I. orthotheciellae</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><th><i>Ochiobryum</i></th><td><i>O. blandum</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>1</td><td>–</td></tr><tr><th><i>Plagiobryoides</i></th><td><i>Bryum gilliesii</i></td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. orbiculatifolia</i></td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>1</td><td>1</td></tr><tr><td><i>Bryum platyphyllum</i></td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th><i>Plagiobryum</i></th><td><i>Bryum lamprocarpum</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>P. novae -seelandiae</i></td><td>–</td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. zierii</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td><td>–</td></tr><tr><th><i>Ptychostomum</i></th><td><i>P. altisetum</i></td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. bimum</i></td><td>1</td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>–</td></tr><tr><td><i>P. chorizodontum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. cernuum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>P. compactum</i></td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>P. creberrimum</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. dicarpum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. donatii</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. eatonii</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>P. gayanum</i></td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. inclinatum</i></td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td><td>1</td><td>1</td></tr><tr><td><i>P. kerguelense</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>P. lamprochaete</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. mucronatum</i></td><td>1</td><td>–</td><td>1</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>P. nivale</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>1</td></tr><tr><td><i>P. orthothecium</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. pallens</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. pallescens</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td><td>1</td></tr><tr><td><i>P. pauperculum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. pseudotriquetrum</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td></tr><tr><td><i>P. tenuidens</i></td><td>–</td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. turbinatum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td><td>–</td></tr><tr><td><i>P. vernicosum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>P. weigelii</i></td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>P. zeballosicum</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th><i>Rhodobryum</i></th><td><i>R.</i> cf. <i>roseodens</i></td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th><i>Rosulabryum</i></th><td><i>R. billarderii</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>–</td><td>1</td><td>–</td></tr><tr><td><i>R. capillare</i></td><td>1</td><td>1</td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td></tr><tr><td><i>R. flaccidum</i></td><td>–</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>R. macrophyllum</i></td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td><i>R. microrhodon</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td></tr><tr><th></th><td><i>R. perlimbatum</i></td><td>1</td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th></th><td><i>R. puconense</i></td><td>1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th></th><td><i>R. rubens</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td></tr><tr><th></th><td><i>R. subtomentosum</i></td><td>–</td><td>–</td><td>1</td><td>1</td><td>–</td><td>–</td><td>–</td></tr><tr><th>Species</th><td></td><td>38</td><td>28</td><td>26</td><td>21</td><td>11</td><td>22</td><td>7</td></tr><tr><th>Endemics</th><td></td><td>11</td><td>3</td><td>2</td><td>2</td><td>1</td><td>4</td><td>0</td></tr></tbody></table>
FIGURE 4 in Lectotypification, taxonomy and distribution of Braunia plicata (Bryopsida, Hedwigiaceae) in South America and Mexico
FIGURE 4. Gametophytic and sporophytic features of Braunia plicata. A–C, I–J) Vegetative leaves. D–E) Perichaetial leaves. F, K) Capsules. G) Upper leaf cells. H) Apical leaf cells. A–H from lectotype Bridges s.n. (BM-herb-Hooker). I–K from Herzog 3703 (JE).
FIGURE 2 in Lectotypification, taxonomy and distribution of Braunia plicata (Bryopsida, Hedwigiaceae) in South America and Mexico
FIGURE 2. Jameson syntype of Braunia plicata. A–B) Vegetative leaves in the Jameson syntype. C) Perichaetial leaf in the Jameson syntype. D–E) Vegetative leaves characteristic of Braunia cirrhifolia. F. Perichaetial leaf of B. cirrhifolia. A–C from Jameson s.n. (syntype of B. plicata, NY-herb. Mitten). D–F from Jameson 1 (BM), type for B. cirrhifolia.
FIGURE 3 in Lectotypification, taxonomy and distribution of Braunia plicata (Bryopsida, Hedwigiaceae) in South America and Mexico
FIGURE 3. Jameson syntype of Braunia plicata. A–B) Leaf cells in the apex and upper leaf, in the Jameson syntype. C–D) Leaf cells in the apex and upper leaf, characteristic of B. cirrhifolia. A–B from Jameson s.n. (syntype of B. plicata, NY-herb. Mitten). C–D from Jameson 1 (BM), type for B. cirrhifolia.
FIGURE 1 in Lectotypification, taxonomy and distribution of Braunia plicata (Bryopsida, Hedwigiaceae) in South America and Mexico
FIGURE 1. Lectotype of Braunia plicata. A) Specimen Bridges s. n., 1846, at BM (herb. Hooker). B) Detail of lectotype, showing one capsule. C) Detail of leaves with hyaline apex. D) Leaf apex hyaline and dentate. (Photographs by E. De Luna).
FIGURES 21–23. Bryobrothera tambuyukonensis. 21 in A new species, Bryobrothera tambuyukonensis (Daltoniaceae, Bryopsida), from Sabah, Borneo Island
FIGURES 21–23. Bryobrothera tambuyukonensis. 21: Axillary hair. 22: Perichaetial leaves. 23: Margin of inner perichaetial leaf. (All from the holotype.)
FIGURE 2 in A new species, Bryobrothera tambuyukonensis (Daltoniaceae, Bryopsida), from Sabah, Borneo Island
FIGURE 2. Strict consensus tree of Maximum parsimony based on date set of rps4, trnL-F, and nad5 sequences. Figures by the nodes are reliabilities estimated by bootstrap methods (1000 duplicates). Leucomium strumosum and Leskeodon cubensis (with asterisks) changes their places in the tree comparing to that obtained from Maximum likelihood method.
FIGURE 3 in A new species, Bryobrothera tambuyukonensis (Daltoniaceae, Bryopsida), from Sabah, Borneo Island
FIGURE 3. ML tree indicating phylogenetic interrelationships among the four species of the genera Adelothecium, Benitotania, and Bryobrothera inferred from the small date set of rps4, trnL-F, and nad5 sequences. Two Ephemeropsis species are attributed as outgroup terminals of these three genera on the basis of results presented by Ho et al. (2012) and Pokorny et al. (2012). Scale bar indicates base substitution.
FIGURE 1 in A new species, Bryobrothera tambuyukonensis (Daltoniaceae, Bryopsida), from Sabah, Borneo Island
FIGURE 1. Maximum likelihood tree based on date set of rps4, trnL-F, and nad5 sequences. Figures by the nodes are reliabilities estimated by bootstrap methods (1000 duplicates). The present new species Bryobrothera tambuyukonensis forms a monophyletic group with Adelothecium, Benitotania, and Bryobrothera.
FIGURE 2. Entosthodon pocsii. 1 in Three new species of Entosthodon Schwägr. (Bryopsida, Funariaceae) from sub-Saharan Africa
FIGURE 2. Entosthodon pocsii. 1. Habit, dry (S. Iversen, E. Persson, B. Petterson & T. Pócs, 87145/D, BOL); 2–5. Leaves (2 ‒ as for 1; 3—5 ‒ S. Iversen, E. Persson, B. Petterson & T. Pócs, 87145/N, BOL); 6, 7. Leaf apex (6 ‒ as for 1; 7 ‒ as for 3); 8. Leaf cross-section (as for 3); 9. Capsule, dry (T. Pócs, D. Harrison & J.M. Mushy 90130/UV, (BOL, EGR); 10. Capsule mouth & peristome (as for 3); 11. Operculum (as for 1); 12. Spores (as for 1). Scale bars: A (2–5) = 500 μm; B (10) = 100 μm; C (1, 9) = 1 mm; D (8) = 100 μm; E (12) = 50 μm; F (11) = 100 μm; G (6, 7) = 100 μm.
FIGURE 1. Entosthodon heddersonii. 1 in Three new species of Entosthodon Schwägr. (Bryopsida, Funariaceae) from sub-Saharan Africa
FIGURE 1. Entosthodon heddersonii. 1. Habit, dry; 2–4. Leaves; 5. Leaf apex; 6. Leaf cross-section; 7. Capsule mouth & peristome (teeth missing in image); 8. Operculum; 9. Spores. All from Holotype. Scale bars: A (2–4) = 500 μm; B (5, 7) = 100 μm; C (1) = 1 mm; D (6) = 100 μm; E (9) = 50 μm; F (8) = 100 μm.
FIGURE 3. Entosthodon zygolimbatus. 1 in Three new species of Entosthodon Schwägr. (Bryopsida, Funariaceae) from sub-Saharan Africa
FIGURE 3. Entosthodon zygolimbatus. 1. Habit, dry; 2–4. Leaves; 5. Leaf apex; 6. Leaf cross-section; 7. Capsule mouth & peristome (teeth missing in image); 8. Spores. All from: T. Pócs, R. Ochyra & H. Bednarek‒Ochyra 88108/M, BOL. Scale bars: A (2–4) = 500 μm; B (5, 7) = 100 μm; C (1) = 1 mm; D (6) = 100 μm; E (8) = 50 μm.
Data from: Maintenance of genetic and morphological identity in two sibling Syrrhopodon species (Calymperaceae, Bryopsida) despite extensive introgression
Bryophytes are a group of land plants wherein the role of hybridization has long been challenged. Using Genotyping by Sequencing to circumvent the lack of molecular variation at selected loci previously used for phylogeny and morphology, we determine the level of genetic and morphological divergence and reproductive isolation between the sibling Syrrhopodon annotinus and S. simmondsii (Calymperaceae, Bryopsida) that occur in sympatry but in different habitats in lowland Amazonian rainforests. A clear morphological differentiation and a low (0.06), but significant Fst derived from the analysis of 183 SNPs were observed between the two species. Conspecific pairs of individuals consistently exhibited higher average kinship coefficients along a gradient of geographic isolation than interspecific pairs. The weak, but significant genetic divergence observed is consistent with growing evidence that ecological specialization can lead to genetic differentiation among bryophyte species. Nevertheless, the spatial genetic structures of the two species were significantly correlated, as evidenced by the significant slope of the Mantel test based on kinship coefficients between pairs of interspecific individuals and the geographic distance separating them. Interspecific pairs of individuals are thus more closely related when they are geographically closer, suggesting that isolation-by-distance is stronger than the interspecific reproductive barrier and pointing to interspecific gene flow. We conclude that interspecific introgression, whose role has long been questioned in bryophytes, may take place even in species wherein sporophyte production is scarce due to dioicy, raising the question as to what mechanisms maintain differentiation despite weak reproductive isolation.
FIGURE 2 in On the systematic position of the genus Timmiella (Dicranidae, Bryopsida) and its allied genera, with the description of a new family Timmiellaceae
FIGURE 2. Opercula (A, C, E, G, I, K) and peristomes (B, D, F, H, J, L) of Timmiella and Luisierella. A, B. Timmiella acaulon. C, D. T. anomala. E, F. T. barbuloides. G, H. T. crassinervis. I, J. T. diminuta. K, L. Luisierella barbula (Peristome teeth indicated by arrowheads). A, B from C. C. Hosseus 396 (HIRO). C, D from Y. Inoue 1910 (HIRO). E, F from C. C. Townsend s.n. (HIRO). G, H from W. B. Schofield 14404 (HIRO). I, J from C. Y. Chang s.n. (TNS). K from R. A. Pursell 632 (HIRO). L from R. L. Redfearn Jr. 73–55 (HIRO). Scale bars = 100 µm.
FIGURE 1 in On the systematic position of the genus Timmiella (Dicranidae, Bryopsida) and its allied genera, with the description of a new family Timmiellaceae
FIGURE 1. Phylogenetic tree based on analysis with the concatenated sequences of chloroplast rps4 and rbcL genes, depicted by a 50% majority-rule consensus tree for the 9 topologies passing both AU and PP tests. Supporting values more than 50% obtained by the program CONSEL were overlaid: the values by the AU test (AU), bootstrap probabilities calculated through the same theory as AU (NP), and Bayesian posterior probabilities (PP) are shown on or near each branch (AU/NP/PP). The root is arbitrarily placed on the branch leading to the clade which includes members of the genera Buxbaumia and Diphyscium following Tsubota et al. (2003, 2004) and Cox et al. (2010).
Data from: Maintenance of genetic and morphological identity in two sibling Syrrhopodon species (Calymperaceae, Bryopsida) despite extensive introgression
Open the record for dataset details and reuse information.
FIGURES 9–20 in A new species, Bryobrothera tambuyukonensis (Daltoniaceae, Bryopsida), from Sabah, Borneo Island
FIGURES 9–20. Bryobrothera tambuyukonensis.
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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.
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DANDI Archive for NWB datasets
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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
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