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95 results for “Hepatica”
Anemone hepatica L. (BR0000012421596)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Analysis and visualization of the Fasciola hepatica spatial transcriptomics dataset
<p>This repository contains various files related to the analysis of the paper: Spatial transcriptomics of a parasitic flatworm provides a molecular map of drug targets and drug-resistance genes.</p>
Table 1 in Patterns of Fasciola hepatica infection in Danish dairy cattle: implications for on-farm control of the parasite based on different diagnostic methods
<p><b>Table 1</b> Summary of data used as inclusion criteria for the 4 farms in the study</p><table><tbody><tr><th>Farm</th><th>Year</th><th>No. of heifers</th><th>No. of cows</th><th>Total no. of cattle</th><th>Liver condemnation (%)</th><th>BTM ELISA value (S/P%)a</th></tr></tbody><tbody><tr><th>C1</th><td>2011</td><td>72.5</td><td>176.5</td><td>314</td><td>6.2</td><td><i>–</i></td></tr><tr><th></th><td>2012</td><td>65.5</td><td>184.5</td><td>303</td><td>21.3</td><td><i>–</i></td></tr><tr><th></th><td>2013</td><td>65</td><td>187.5</td><td>315</td><td>30.0</td><td><i>–</i></td></tr><tr><th></th><td>2014</td><td>63</td><td>183.5</td><td>312</td><td>18.6</td><td>179.3</td></tr><tr><th>C2</th><td>2011</td><td>103</td><td>135</td><td>292</td><td>8.3</td><td><i>–</i></td></tr><tr><th></th><td>2012</td><td>98.5</td><td>145</td><td>300</td><td>11.9</td><td><i>–</i></td></tr><tr><th></th><td>2013</td><td>105.5</td><td>144</td><td>314</td><td>16.1</td><td><i>–</i></td></tr><tr><th></th><td>2014</td><td>111</td><td>149</td><td>331</td><td>19.4</td><td>181.2</td></tr><tr><th>O1</th><td>2011</td><td>145</td><td>172</td><td>367</td><td>2.6</td><td><i>–</i></td></tr><tr><th></th><td>2012</td><td>141</td><td>168</td><td>362</td><td>7.6</td><td><i>–</i></td></tr><tr><th></th><td>2013</td><td>124</td><td>174.5</td><td>354</td><td>33.3</td><td><i>–</i></td></tr><tr><th></th><td>2014</td><td>172</td><td>183</td><td>425</td><td>23.3</td><td>221.4</td></tr><tr><th>O2</th><td>2011</td><td>90.5</td><td>113.5</td><td>251</td><td>18.1</td><td><i>–</i></td></tr><tr><th></th><td>2012</td><td>97.5</td><td>124</td><td>275</td><td>32.6</td><td><i>–</i></td></tr><tr><th></th><td>2013</td><td>111</td><td>131.5</td><td>282</td><td>27.7</td><td><i>–</i></td></tr><tr><th></th><td>2014</td><td>113</td><td>133.5</td><td>285</td><td>38.1</td><td>206.9</td></tr></tbody></table><p><sup>a</sup> by IDEXX ELISA test (cut-off is 30 and ≥ 150S/P% is considered high)</p>
FIGURE 9. Oxalis hepatica. A in Taxonomic revision and morphological delimitation of Oxalis sect. Ripariae (Oxalidaceae)
FIGURE 9. Oxalis hepatica. A—habit; B—leaf abaxial (left), adaxial (right) surfaces, and inflorescence; C—leaf abaxial surface; D— abaxial leaflet insertions detail, pulvina (arrowhead); E—longistylous flower, frontal view; F—leaf insertion at stem detail, showing stipule; G—inflorescence in bud; H—floral bud in pre-anthesis, showing glandular hairs on perianth; I—detail of leaflet abaxial surface; J—peduncle with bracts (arrowhead); K. stem indumentum detail. Photos: A–B, D, F, I–L. A. Nuernberg-Silva; C, E, G–H. P. Fiaschi.
FIGURE 3 in A new Mylia Gray (Myliaceae, Hepaticae) species from North Vietnam extends the range of the genus to the Paleotropics
FIGURE 3 Mylia vietnamica Bakalin et Vilnet: 1—plant habit in dry condition (glistening stem is visible), 2—fissured leaf cuticle, 3—cells in the midleaf, 4—leaf margin, 5—underleaf; from Holotype (V-3-36-16, VBGI). Mylia taylorii (Hook.) Gray: 6, 7—leaf margin, 8—midleaf cells; from Khabarovsk Territory (Kh-18-22-16, VBGI). Scales: a—100 μm, for 2–8; b—2 mm, for 1.
FIGURE 2 in A new Mylia Gray (Myliaceae, Hepaticae) species from North Vietnam extends the range of the genus to the Paleotropics
FIGURE 2 Mylia vietnamica Bakalin et Vilnet: 1, 2—plant habit, 3—stem cross section (fragment), 4–8—leaves. Scales: a—2 mm, for 1,2, 4–8; b—100 μm, for 3. All from Holotype (V-3-36-16, VBGI).
FIGURE 1 in A new Mylia Gray (Myliaceae, Hepaticae) species from North Vietnam extends the range of the genus to the Paleotropics
FIGURE 1 Phylogram obtained in a maximum likelihood calculation for the genus Mylia based on the combined dataset of ITS1-2 nrDNA and trnL-F cpDNA nucleotide sequences. Bootstrap support values more than 50% (0.50) and length of cut branches are indicated.
FIGURE 16. Drouetiella hepatica. A in Revision of the Synechococcales (Cyanobacteria) through recognition of four families including Oculatellaceae fam. nov. and Trichocoleaceae fam. nov. and six new genera containing 14 species
FIGURE 16. Drouetiella hepatica. A. Heterogeneity in trichome width between young and mature filaments, young filaments isodiametric to slightly cylindrical. B–C. False-branching very rare in young trichomes, only single false-branches observered. D–F. Sheath sometimes elongated and lamellate as in (E). G. Rapid cell division in meristematic zones sometimes caused twisted trichomes. H. Frequent necridia occur along actively dividing trichomes. Scale bar 10μm in 1000X magnification.
FIGURE 3 in Austral Hepaticae 50. Gackstroemia in New Zealand, together with an interesting new species
FIGURE 3. Gackstroemia weindorferi (Herzog) Grolle. 1. Two leaf pairs of main shoot, dorsal view; note dorsally interlocking insertion lines and plane and not reflexed dorsal margin of dorsal lobes. 2. Two leaf pairs of main shoot, ventral view (underleaves removed for clarity, only the scars indicated); note first branch underleaf (= fbu); (drawn to same scale as fig. 1). 3. Leaf from main shoot. 4. Median cells of dorsal lobe. 5. Underleaf, in situ, of main shoot, ventral view. 6. Underleaf. 7. Distal sector of underleaf lobe. 8. Tertiary branch showing saccate lobes of both first branch underleaf and underleaves of branch (ventral view). Note the bilobed first branch underleaf (= fbu) of the secondary branch (= 2º br), and the next two underleaves of the branch, the first bilobed similar to the first branch underleaf, the second with both lobes saccate. Underleaf scars are shown on short sector of primary branch (= 1º br). 9. Innermost bracts. 10. Perianth (flattened). 11. Spore and elater drawn to same scale; note proximal face. 12. Elater. (Figs. 1, 2, 5, 8, from Engel 19039A, New Zealand, South Is., Westland Prov., Paparoa Range, ridge immediately N of Sewell Peak; 3, 6, 7, from Engel 13154, Tasmania, E side of Tasman Peninsula, W facing, upper slope of Tatnells Hill; 4, 9-12, from Engel 12912, Tasmania, Mt. Field National Park, off Lake Dobson Road.)
FIGURE 1. Gackstroemia novae-zelandiae R.M.Schust. & J.J.Engel. 1 in Austral Hepaticae 50. Gackstroemia in New Zealand, together with an interesting new species
FIGURE 1. Gackstroemia novae-zelandiae R.M.Schust. & J.J.Engel. 1. Sector of shoot with Frullania-type branch (note first branch underleaf), ventral view. Note also the flattened, lamelliform stylus. 2. Leaf pair of main shoot, dorsal view; note dorsally interlocking insertion lines and reflexed dorsal margin of dorsal lobes. 3, 4. Leaves from main shoot (dm = dorsal margin). 5. Median leaf cells. 6. Dorsal margin of leaf from main shoot. 7. Underleaf, in situ of main shoot (drawn to same scale as fig. 1). 8. Underleaf. 9, 10. Distal sector of underleaf lobes. 11. Tertiary branch (= 3º br) showing explanate lobes of first branch underleaf (= fbu) and explanate underleaves of branch, ventral view (LB = leaf base). (Fig. 3 from Engel 21925, New Zealand, South Is., Otago Prov., Mt. Aspiring Natl. Park, Blue Valley Track; remainder from holotype.)
FIGURE 2. Gackstroemia novae-zelandiae R.M.Schust. & J.J.Engel. 1 in Austral Hepaticae 50. Gackstroemia in New Zealand, together with an interesting new species
FIGURE 2. Gackstroemia novae-zelandiae R.M.Schust. & J.J.Engel. 1. Portion of main shoot with gynoecium pseudolateral in position through growth of a pseudo-innovation (= pi); note also the Frullania-type branch (= FB; hl = half leaf), (dorsal view). The gynoecium forming a sporophyte-bearing coelocaule tightly invested by mutually, strongly imbricated bracts and bracteoles. Note form of capsule valves are coherent at apex, both in wet and (to left) dry conditions. 2. Coelocaule (dorsal view) with bract insertions indicated by scars, and, at summit, a perianth-like structure (the bract margins not fused on the ventral side, see fig. 3). Note also the copious cilia at the perianth mouth. 3. Ventral side of a perianth-like structure shown in fig. 2, note that bract margins are not fused. 4. Portion of perianth mouth. 5. Cilia of perianth mouth. 6. Capsule wall, cross section, the outermost layer of intermediate cells ± in tact, but those within for the most part collapsed. 7. Capsule wall, outer layer. 8. Capsule wall, inner layer. 9. Spore and to left, portion of elater drawn to same scale. 10. Elater. (All from holotype.)
FIGURE 3 in The transfer of Tritomaria koreana to Lophozia has led to recircumscription of the genus and shown convergence in Lophoziaceae (Hepaticae)
FIGURE 3. Lophozia koreana (Bakalin, S.S. Choi et B.-Y. Sun) Bakalin, Maltseva et Vilnet: A—oil bodies in the midleaf cells; B, F—mat, plants with gemmae; C—gemmae; D—mat; E, G—leaves. Scales:50 µm for A, C; 500 µm for E, G; 1 mm for B, D; 5 mm for F. A, B, C, E, G from Bakalin Kor-75-15-19 (VBGI); D from Bakalin Kor-74-5-19 (VBGI); F from Bakalin J-87-13-15 (VBGI).
FIGURE 1 in The transfer of Tritomaria koreana to Lophozia has led to recircumscription of the genus and shown convergence in Lophoziaceae (Hepaticae)
FIGURE 1. Phylogram obtained in a Bayesian analysis for the genus Lophozia and related taxa based on the combined ITS1–2+trnL-F dataset. The values of bootstrap support from the MP and ML analyses and Bayesian posterior probabilities greater than 50% (0.50) are indicated. Newly studied specimens are marked in red.
Large-scale phylogenomics reveals ancient introgression in Asian Hepatica and new insights into the origin of the insular endemic Hepatica maxima
<p><i>Hepatica maxima</i> is native to Ulleungdo, which is one of the oceanic islands in Korea, and it likely originated via anagenetic speciation from the Korean mainland species <i>H. asiatica</i>. However, the relationships among the Asian lineages remain unresolved. Phylogenomics based on plant genomes can provide new insights into the evolutionary history of plants. We first generated plastid, mitochondrial and transcriptome sequences of the insular endemic species <i>H. maxima</i>. Using the genomic data for <i>H. maxima</i>, we obtained a phylogenomic dataset consisting of 76 plastid, 37 mitochondrial and 413 nuclear genes from Asian <i>Hepatica</i> and two outgroups. Coalescent- and concatenation-based methods revealed cytonuclear and organellar discordance in the lineage. The presence of gynodioecy with cytoplasmic male sterility in Asian <i>Hepatica</i> suggests that the discordance is correlated with potential disruption of linkage disequilibrium between the organellar genomes. Species network analyses revealed a deep history of hybridization and introgression in Asian <i>Hepatica.</i> We discovered that ancient and recent introgression events occurred throughout the evolutionary history of the insular endemic species <i>H. maxima</i>. The introgression may serve as an important source of genetic variation to facilitate adaptation to the Ulleungdo environment.</p>
Large-scale phylogenomics reveals ancient introgression in Asian Hepatica and new insights into the origin of the insular endemic Hepatica maxima
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Hepatica nobilis Miller (BR0000012340668)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Hepatica nobilis Miller (BR0000020280604)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Hepatica nobilis Miller (BR0000011140870)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Hepatica nobilis Miller (BR0000012198085)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Hepatica nobilis Miller (BR0000011851240)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.