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116 results for “endophytic fungi”
Fig. 6 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 6. (continued).
Fig. 3 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 3. (continued).
Fig. 5 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 5. Sesterterpenoids.
Fig. 4 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 4. (continued).
Fig. 8 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 8. Other terpenoids.
Fig. 6 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 6. (continued).
Fig. 3 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 3. (continued).
Data from: Endophytic-insect parasitic fungi translocate nitrogen directly from insects to plants
Open the record for dataset details and reuse information.
Figure 1 from: Tibpromma S, Hyde K, Bhat J, Mortimer P, Xu J, Promputtha I, Doilom M, Yang J, Tang A, Karunarathna S (2018) Identification of endophytic fungi from leaves of Pandanaceae based on their morphotypes and DNA sequence data from southern Thailand. MycoKeys 33: 25-67. https://doi.org/10.3897/mycokeys.33.23670
Figure 1 Habitats of the host plants: a, b Pandanus spp. c, d Freycinetia spp.
Figure 1 from: Tibpromma S, Hyde K, Bhat J, Mortimer P, Xu J, Promputtha I, Doilom M, Yang J, Tang A, Karunarathna S (2018) Identification of endophytic fungi from leaves of Pandanaceae based on their morphotypes and DNA sequence data from southern Thailand. MycoKeys 33: 25-67. https://doi.org/10.3897/mycokeys.33.23670
Figure 1 - Habitats of the host plants: a, b Pandanus spp. c, d Freycinetia spp.
FIGURE 6 in Two new endophytic fungi of Colletotrichum and Diaporthe isolated from Berchemia polyphylla var. leioclada in Guizhou Province, China
FIGURE 6. Results of the PHI test of Diaporthe berchemiae and closely related species using both LogDet transformation and splits decomposition. The PHI test results (Φw) <0.05 indicate significant recombination within the dataset. The new taxa are in red.
FIGURE 8 in Endophytic fungi associated with Coriaria nepalensis in an abandoned open-pit phosphate mine in Yunnan, P.R. China
FIGURE 8. Epicoccum nigrum (HKAS 129062). (a,b) Obverse and reverse of colony on PDA; (a–b) Close up of the fruiting bodies on PDA; (e,f) Conidiogenous cells bearing conidia; (g) Mycelium; (h–m) Conidia.
FIGURE 5 in Endophytic fungi associated with Coriaria nepalensis in an abandoned open-pit phosphate mine in Yunnan, P.R. China
FIGURE 5. Phylogram generated from Maximum Likelihood analysis based on a combined LSU, ITS, rpb2 and tub2 sequence datasets. The 70 strains are included in the combined gene analysis 2460 total character including gaps (LSU: 1–590 bp, ITS: 591–1128 bp, rpb2: 1129–1730 bp, tub2: 1731–2460 bp). Tree topology of the ML analysis was similar to the BI. The matrix had distinct alignment patterns, with the final ML optimization likelihood value of -13768.250026 (ln). All free model parameters were estimated by RAxML model, with 828 distinct alignment patterns and 11.11% of undetermined characters or gaps. Estimated base frequencies were as follows: A = 0.236385, C =0.275681, G = 0.277948, T = 0.209986, with substitution rates AC = 1.091927, AG = 4.082662, AT = 1.184028, CG = 1.265089, CT = 7.046047, GT = 1.000000. The gamma distribution shape parameter alpha = 0.760807 and the Tree-Length = 1.234745. The final average standard deviation of split frequencies at the end of total MCMC generations was calculated as 0.009913 in BI analysis. The species introduced in this study are indicated in red, and the type strains are indicated in bold. Bootstrap values greater than 60% (ML, Left) and Bayesian posterior probabilities (BI, right) greater than 0.95 are given at the nodes. Hypens (-) represent values less than 60% in ML/0.95 in BI.
FIGURE 3 in Endophytic fungi associated with Coriaria nepalensis in an abandoned open-pit phosphate mine in Yunnan, P.R. China
FIGURE 3. Phylogram generated from Maximum Likelihood analysis based on a combined LSU, ITS, rpb2 and tef1-α sequence datasets. The 49 strains are included in the combined gene analysis 2675 total character including gaps (LSU: 1–858 bp, ITS: 859–1493 bp, rpb2: 1494–2264 bp, tef1-α: 2265–2675 bp). Tree topology of the ML analysis was similar to the BI. The matrix had distinct alignment patterns, with the final ML optimization likelihood value of -17797.249759 (ln). All free model parameters were estimated by RAxML model, with 1009 distinct alignment patterns and 20.15% of undetermined characters or gaps. Estimated base frequencies were as follows: A = 0.251880, C = 0.239731, G = 0.262605, T = 0.245784, with substitution rates AC = 1.333861, AG = 3.064614, AT = 1.306478, CG = 0.734024, CT = 6.282119, GT = 1.000000. The gamma distribution shape parameter alpha = 0.181243 and the Tree-Length = 2.594332. The final average standard deviation of split frequencies at the end of total MCMC generations was calculated as 0.009897 in BI analysis. The species introduced in this study are indicated in red, and the type strains are indicated in bold. Bootstrap values greater than 60% (ML, Left) and Bayesian posterior probabilities (BI, right) greater than 0.95 are given at the nodes. Hypens (-) represent values less than 60% in ML/0.95 in BI.
Fig. 3 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 3. (continued).
Fig. 3 in Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011-2020)
Fig. 3. (continued).
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