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1,918 results for “molecular evidence”
FIGURE 2 in Cymbidium biflorens (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data
FIGURE 2. Phylogenetic relationships of C. biflorens based on the combined plastid DNA. The numbers near the nodes are Bayesian
FIGURE 3 in Cymbidium biflorens (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data
FIGURE 3. Phylogenetic relationships of C. biflorens based on the nuclear DNA (ITS). The numbers near the nodes are Bayesian posterior probabilities (PP), maximum likelihood bootstrap percentages (BP) and maximum parsimony bootstrap percentages (BP). ML MP "*" indicates that the node has BP 100 or PP 1.00. "-" indicates that the node is incongruent between the Bayesian and MP/ML trees.
FIGURE 1 in Liparis mai (Orchidaceae; Malaxideae), a new species from China: evidence from morphological and molecular analyses
FIGURE 1. Phylogenetic tree obtained by maximum-likelihood analysis of the combined matrix. Numbers near the nodes are bootstrap percentages and Bayesian posterior probabilities (BP, BP, PP). A dash (–) indicates a node is inconsistent between the topology of the ML MP ML/MP and the Bayesian trees. An asterisk (*) indicates a node is 100 bootstrap percentage or 1.00 posterior probability.
FIGURE 3. Liparis mai X.D in Liparis mai (Orchidaceae; Malaxideae), a new species from China: evidence from morphological and molecular analyses
FIGURE 3. Liparis mai X.D.Tu, M.Z.Huang & M.H.Li. A. Plant. B. Flower, front view. C. Flower, side view. D. Dorsal sepal, petal, lateral sepal, and lip. E. Pollinarium. F. Bulbil.
FIGURE 2. Liparis mai X.D in Liparis mai (Orchidaceae; Malaxideae), a new species from China: evidence from morphological and molecular analyses
FIGURE 2. Liparis mai X.D.Tu, M.Z.Huang & M.H.Li. A. Plant. B. Dorsal sepal, petal, lateral sepal, lip, Anther cap and pollinarium. C. Bulbil, front view. D. Bulbil side view. E. Flowers. F. callus. G. Flower, front view. H. Flower, side view.
FIGURE 2 in Molecular and morphological evidence for a new species in the genus Sirodotia (Batrachospermales, Rhodophyta) from the State of Assam, India
FIGURE 2. Distance tree (neighbor joining) of COI-5P DNA sequences for Sirodotia species and Batrachospermales outgroup taxa. The numbers associated with the nodes indicate the bootstrap values, nodes without values indicate support <70%. Sample codes as in Table 1.
FIGURE 1 in Molecular and morphological evidence for a new species in the genus Sirodotia (Batrachospermales, Rhodophyta) from the State of Assam, India
FIGURE 1. Maximum likelihood phylogenetic tree based on rbcL DNA sequences. The numbers associated with the nodes indicate the bootstrap values (BS) for maximum likelihood and posterior probability (PP) for Bayesian analysis, respectively. Nodes without values indicate BS ≤ 70% and PP ≤ 0.70. Sample codes as in Table 1.
FIGURE 3 in Molecular and morphological evidence for a new species in the genus Sirodotia (Batrachospermales, Rhodophyta) from the State of Assam, India
FIGURE 3. Sirodotia assamica sp. nov. a. Main axis. b. Whorl showing densely arranged gonimoblast filaments along the internode (arrow). c. Primary fascicles and spermatangia (Sp) in clusters on a primary fascicle. d. Carposporangia (Cp), prostrate (Pr) and erect (Er) gonimoblast filaments. e. Detail of spermatangia (Sp) in clusters on primary fascicle. f. Spermatangia (Sp) in clusters on a secondary fascicle. g. A carpogonium with a mature trichogyne (Tr) and a basal hemispherical protuberance (PB). h. Fertilized carpogonium with attached spermatium and gonimoblast initial (GI) on the same side of the basal protuberance. Scale bar: 100 µm for figure a; 50 µm for figures b, c and f; 20 µm for figures d,e,g and h.
FIGURE 1 in Morphological and Molecular Evidence for a New Species of Dianthus (Caryophyllaceae) from Turkey
FIGURE 1. The ML tree showing the genetic relationships of Dianthus hamzaoglui, 6 Dianthus taxa and the outgroup Silene acaulis based on the ITS region.
FIGURE 5 in Morphological and Molecular Evidence for a New Species of Dianthus (Caryophyllaceae) from Turkey
FIGURE 5. Distribution of Dianthus hamzaoglui (■), D. masmenaeus (●) and D. burdurensis (▲) in Turkey.
FIGURE 4 in Morphological and Molecular Evidence for a New Species of Dianthus (Caryophyllaceae) from Turkey
FIGURE 4. SEM photographs of the seed coat. (A) Dianthus hamzaoglui, (B) Dianthus burdurensis. Scale bars: 1 and 4 = 100 μm; 2, 3, 5, and 6 = 20 μm. (Dianthus burdurensis seed photographs taken from the Hamzaoğlu & Koç 2015)
FIGURE 4. Phylogenetic tree with bootstrap values inferred from trnL-F in Revisit of European-Asiatic connections in Tayloria rudolphiana (Splachnaceae, Bryophyta) based on molecular data and new morphological evidence
FIGURE 4. Phylogenetic tree with bootstrap values inferred from trnL-F sequences (accession numbers after each species name obtained from Genbank) based on Maximum Likelihood and Maximum Parsimony analyses. Values above the branches indicate bootstrap (>50%) and numbers below the branches indicate PP values of Bayesian.
FIGURE 3. Phylogenetic tree with bootstrap values inferred from rps4 in Revisit of European-Asiatic connections in Tayloria rudolphiana (Splachnaceae, Bryophyta) based on molecular data and new morphological evidence
FIGURE 3. Phylogenetic tree with bootstrap values inferred from rps4 sequences (accession numbers after each species name obtained from Genbank) based on Maximum Likelihood and Maximum Parsimony analyses. Values above the branches indicate bootstrap (>50%) and numbers below the branches indicate PP values of Bayesian.
FIGURE 1. Tayloria rudolphiana. A in Revisit of European-Asiatic connections in Tayloria rudolphiana (Splachnaceae, Bryophyta) based on molecular data and new morphological evidence
FIGURE 1. Tayloria rudolphiana. A. Habit in field. B. Dry habit (left); wet habit (right). C. Perichaetial leaves. D. Upper leaves. E. Low leaves. F–G. leaf apices. H. Midleaf. I. Basal leaf. J. Juxtacostal cells at midleaf. K. Median laminal cells. L. Basal laminal cells. (All photo images prepared from He & Yi 49798, MO).
FIGURE 2. Dendrobium yongjiaense Z.Zhou & S.R.Lan. A. Plant. B. Flower, front view. C. Flower with lateral sepals removed, side view. D. Lip, front view. E. Petal. F. Dorsal sepal. G. Lateral sepal. H. Column, front view. I in Morphological and molecular evidence for a new species from China: Dendrobium yongjiaense (Orchidaceae: Malaxideae)
FIGURE 2. Dendrobium yongjiaense Z.Zhou & S.R.Lan. A. Plant. B. Flower, front view. C. Flower with lateral sepals removed, side view. D. Lip, front view. E. Petal. F. Dorsal sepal. G. Lateral sepal. H. Column, front view. I. Pollinarium. Drawn by Zhuang Zhou.
FIGURE 1 in Morphological and molecular evidence for a new species from China: Dendrobium yongjiaense (Orchidaceae: Malaxideae)
FIGURE 1. Phylogenetic tree obtained by maximum-likelihood analysis of the combined matrix. Separate nrITS (A) and combined plastid (B) results are shown in the top left corner. Numbers near the nodes are bootstrap percentages and Bayesian posterior probabilities (BP, PP, and BP). A dash (-) indicates a node is inconsistent between the topology of the MP/ML trees and the Bayesian tree; * node ML MP is 100 bootstrap percentage or 1.00 posterior probability.
TABLE 1 in Two new diploid species of Isoetes (Isoetaceae: Lycopodiopsida) from Southeastern China based on morphological and molecular evidence
<p><b>TABLE 1.</b> Comparative accounts on the morphology of megaspores and microspores of <i>Isoetes</i> species in China.</p><table><tbody><tr><th></th><th><i>I. changleensis</i></th><th><i>I. yuhangensis</i></th><th><i>I. baodongii</i></th><th><i>I. sinensis</i></th><th><i>I. longpingii</i></th><th><i>I. xiangfei</i></th><th><i>I. orientalis</i></th><th><i>I. taiwanensis</i></th><th><i>I. yunguiensis</i></th><th><i>I. hypsophila</i></th><th><i>I. shangrilaensis</i></th></tr></tbody><tbody><tr><th>Megaspore diameter (μm)</th><td>246–314</td><td>270–324</td><td>390–510</td><td>317–424</td><td>310–410</td><td>390–450</td><td>350–460</td><td>280–340</td><td>340–430</td><td>361–510</td><td>207–273</td></tr><tr><th>Mean megaspore size (μm)</th><td>284</td><td>302</td><td>450</td><td>378</td><td>350</td><td>430</td><td>420</td><td>312</td><td>390</td><td>450</td><td>245</td></tr><tr><th>Ornamentation of megaspores</th></tr><tr><th>proximal surface</th><td>tuberculate</td><td>rugulate</td><td>echinate-cristate</td><td>echinate</td><td>tuberculate-cristate</td><td>cristate-reticulate</td><td>cristate-reticulate</td><td>tuberculate</td><td>cristate-reticulate</td><td>levigate</td><td>levigate</td></tr><tr><th>Equatorial surface (girdle)</th><td>rugulate</td><td>smooth</td><td>/</td><td>loss</td><td>/</td><td>/</td><td>/</td><td>smooth</td><td>loss</td><td>loss</td><td>smooth</td></tr><tr><th>distal surface</th><td>rugulate</td><td>rugulate</td><td>echinate-cristate</td><td>echinate-cristate</td><td>tuberculate-cristate</td><td>cristate-reticulate</td><td>cristate-reticulate</td><td>tuberculate-cristate</td><td>cristate-reticulate</td><td>levigate</td><td>tuberculate-rugulate</td></tr><tr><th>Range microspore size (μm)</th><td>14–20</td><td>16–26</td><td>22–27</td><td>20–29</td><td>27–30</td><td>26–28</td><td>20–38</td><td>20–28</td><td>20–25</td><td>19–25</td><td>11–24</td></tr><tr><th>Mean microspore size (μm)</th><td>18</td><td>21</td><td>25</td><td>25</td><td>29</td><td>27</td><td>34</td><td>24</td><td>22</td><td>22</td><td>19</td></tr><tr><th>Ornamentation of microspores</th><td>blunt-tipped echinate</td><td>sharp-tipped echinate</td><td>echinate</td><td>echinate</td><td>echinate</td><td>echinate</td><td>echinate-tuberculate</td><td>echinate</td><td>levigate-granulate</td><td>rugulate</td><td>echinate-cristate</td></tr><tr><th>Chromosome number</th><td>22</td><td>22</td><td>22</td><td>44</td><td>44</td><td>44</td><td>66</td><td>22</td><td>22</td><td>22</td><td>22</td></tr><tr><th>Data Source</th><td>this study</td><td>this study</td><td>Lu <i>et al.</i> 2021</td><td>Liu <i>et al.</i> 2008</td><td>Shu <i>et al.</i> 2022</td><td>Shu <i>et al.</i> 2022</td><td>Liu <i>et al.</i> 2008</td><td>Liu <i>et al.</i> 2008</td><td>Liu <i>et al.</i> 2008</td><td>Li <i>et al.</i> 2019</td><td>Li <i>et al.</i> 2019 Shu <i>et al.</i> 2022</td></tr></tbody></table><p>Note:/ represents no data.</p>
FIGURE 3. Dendrobium yongjiaense Z.Zhou & S.R.Lan. A. Flowering plant. B. Inflorescences. C in Morphological and molecular evidence for a new species from China: Dendrobium yongjiaense (Orchidaceae: Malaxideae)
FIGURE 3. Dendrobium yongjiaense Z.Zhou & S.R.Lan. A. Flowering plant. B. Inflorescences. C. Anatomy of the flower. D. Lip, side view. E. Pollinarium. F. Flower, front view. G. Flower with lateral sepals removed, side view. H. Column, front view. I. Lip, front view (left) and basal view (right). J–K. Anther cap, different view.
FIGURE 2. Tayloria rudolphiana. A. Young sporophyte. B. Calyptra. C–D. Capsules. E. Columella with spore sac. F. Peristome teeth. G. Stomata. H. Axillary hairs. I in Revisit of European-Asiatic connections in Tayloria rudolphiana (Splachnaceae, Bryophyta) based on molecular data and new morphological evidence
FIGURE 2. Tayloria rudolphiana. A. Young sporophyte. B. Calyptra. C–D. Capsules. E. Columella with spore sac. F. Peristome teeth. G. Stomata. H. Axillary hairs. I. Cross sections of stem. J. Cross sections of leaves at midleaf. (All photo images prepared from He & Yi 49798, MO).
FIGURE 5 in Satureja kermanica (Lamiaceae) a new species from south-east of Iran, inferred from molecular and morphological evidence
FIGURE 5. Bayesian consensus tree from ITS of Satureja species. Data above branches are the value from Bayesian inference (BI). Green color represents S. kermanica sp. nov. "S" is the abbreviation of Satureja. The geographical area of distribution for S. bachtiarica and the herbarium numbers for the accessions sequenced in this study are presented.
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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.