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101 results for “Musa”

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zenodo32/100

FIGURE 1. Musa balbisiana var. elavazhai. A. habit. B in A new variety of Musa balbisiana Colla (Musaceae) from South India

FIGURE 1. Musa balbisiana var. elavazhai. A. habit. B. pseudostem color at young stage. C. color at maturity. D. leaf apex. E. leaf base. F. cross-section of petiole, G. inflorescence at emerging stage. H–M. female flower parts. H. entire flower. I–J compound tepal. K. flower without tepals. L. free tepal. M. cross-section of ovary. N–O. bract. P–Q. male flower parts. P. entire flower. Q. flower without tepals. R. inflorescene at advanced blooming. S. fruit bunch. T. single fruit. U. seeds. Photos by Alfred Joe.

opennotspecifiedJul 2014View details →
zenodo32/100

FIGURE 1. Musa cylindrica. A. habit. B. pseudostem. C in Musa cylindrica, a new species of Musa (Musaceae) from North-East India

FIGURE 1. Musa cylindrica. A. habit. B. pseudostem. C. cross-section of petiole. D. leaf apex. E. leaf base. F. female bud at early stages. G. female bud. H. male bud at advanced blooming. I–M. female flower parts. I. entire flower. J. compound tepal. K. free tepal. L. flower without tepals. M. cross-section of ovary. N–P. male flower parts. N. entire flower. O. compound tepal. P. flower without tepals. Q. inflorescence. R. fruit bunch. S. seeds. Photos by Alfred Joe.

opennotspecifiedJun 2014View details →
zenodo32/100

FIGURE 4 in Musa ruiliensis (Musaceae, Section Musa), a new species from Yunnan, China

FIGURE 4. Strict consensus tree of Musaceae inferred from 3cpDNA sequences. The numbers associated to each node represent bootstraps and Posterior Probability (values below 50/0.50 are not shown and indicated as ''-"). Letters after the names of Musa species: M and C represent Section Musa and Section Callimusa respectively, which are followed by their relevant chromosome numbers. The clade containing species involved in this study is marked in red.

opennotspecifiedJun 2014View details →
zenodo32/100

FIGURE 1 in Musa ruiliensis (Musaceae, Section Musa), a new species from Yunnan, China

FIGURE 1. The morphological comparisons of Musa ruiliensis and its close sister species. A. Inflorescence with flowers and fruit of M. ruiliensis. B. Inflorescence and fruit of M. chunii. C. Petiole basis and inflorescence with male bud and fruit of M. rubinea. D. Female flower and inflorescence with male bud of M. zaifui. Photos by X.J. Ge: A, and M. Häkkinen: B–D.

opennotspecifiedJun 2014View details →
zenodo32/100

FIGURE 2 in Phyllosticta species from banana (Musa sp.) in Chongqing and Guizhou Provinces, China

FIGURE 2. The first of 2496 equally most parsimonious trees obtained from a heuristic search with 1000 random taxon additions of the ITS, ACT, TEF-1 and GPDH sequences using PAUP v. 4.0b10. The scale bar shows 20 changes. Bootstrap support values for maximum parsimony (MPBS) and maximum likelihood (MLBS)(equal to or above 50 %)were shown. Thickened branches represent significant Bayesian posterior probability (≥90%). A hyphen (–) indicates the value lower than 50%. The tree is rooted Botryosphaeria dothidea.An asterisk (*) indicates the ex-type strains. Novel sequences are printed in bold.

opennotspecifiedDec 2014View details →
zenodo32/100

FIGURE 1. The most parsimonious trees obtained from a heuristic search with 1000 in Phyllosticta species from banana (Musa sp.) in Chongqing and Guizhou Provinces, China

FIGURE 1. The most parsimonious trees obtained from a heuristic search with 1000 random taxon additions of the LSU sequences using PAUP v. 4.0b10. The scale bar shows 5 changes. Bootstrap support values for maximum parsimony (MP) and Bayesian posterior probabilities above 0.90are shown. A hyphens (–) indicates the value lower than 50% (BS) or 0.90 (PP). The tree is rooted to Botryosphaeria dothidea. Ex-type/ex-epitype isolates are marked by an asterisk *. Novel sequences are in boldface.

opennotspecifiedDec 2014View details →
zenodo32/100

FIGURE 3 in Phyllosticta species from banana (Musa sp.) in Chongqing and Guizhou Provinces, China

FIGURE 3.Phyllosticta musaechinensis (CQ12097, holotype).a. Symptom of disease. b. Pycnidia on infected leaf of Musa sp. c, d. Ostiole of pycnidium. e. Pycnidium and conidiogenous cell. f–h. Conidia. i. Conidia on colony. j. Conidiogenous cell in culture. k. Conidia from culture. l–n. Culture on PDA. Scale bars: e = 50µm, f–h, j, k = 20 µm, n = 5 mm.

opennotspecifiedDec 2014View details →
zenodo32/100

Inputs (forcing and observations) ready for use by 'MuSA: The Multiscale Snow Data Assimilation System (v1.0)'

<p>MuSA is a snow data assimilation system that can fuse observations with snowpack simulations generated by the Flexible Snow Model (FSM2). This repository contains meteorological forcing developed with the Micromet model and 5 m resolution snow depth observations in the Izas basin (central Spanish Pyrenees) generated with drones, ready to be used in MuSA.</p>

opencc-by-4.0Aug 2022View details →
zenodo32/100

Fig. 4 in Assessment of metabolic variability and diversity present in leaf, peel and pulp tissue of diploid and triploid Musa spp.

Fig. 4. PCA analysis of leaf (A), peel (B) and pulp (C) of different Musa varieties. Data included metabolites identified by UPLC and LC-MS for all tissues and additional metabolites analysed by GC-MS for peel and pulp. PCA analysis of peel (B) is displayed in two plots: with all varieties (top plot) and without the outliers Petite Naine (ITC0654), Mbwazirume (ITC0084) and Blue Java (ITC0361) (bottom plot). Varieties are marked by genome group, see legend.

opennotspecifiedAug 2020View details →
zenodo32/100

Fig. 1 in Assessment of metabolic variability and diversity present in leaf, peel and pulp tissue of diploid and triploid Musa spp.

Fig. 1. PCA analysis of leaf 1 to 9 comparing Mbi egome (stars) and Fougamou (circles) at three plant growth stages. The three plant growth stages comprised preflowering, flowering and harvest stage (colours displayed in legend). Data includes 76 metabolites analysed by UPLC-DAD and GC-MS (polar extracts). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedAug 2020View details →
zenodo32/100

Fig. 3 in Assessment of metabolic variability and diversity present in leaf, peel and pulp tissue of diploid and triploid Musa spp.

Fig. 3. Metabolites detected by three analytical platforms in leaf, peel and pulp of 18 Musa varieties. The analytical platforms included LC-MS, GC-MS and UPLCDAD. Metabolites are coloured by highest expression in a specific tissue (leaf-green, peel-orange and pulp-yellow) and no difference between tissue types (grey). Metabolites not detected with any analytical platform show no colouration. Roman numbers indicate isomeric metabolites: chlorogenic acid and violaxanthin (geometric isomers) and rutin and kaempferol-glucoside and –rutinoside (constitutional isomers of sugars). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedAug 2020View details →
zenodo32/100

Fig. 2 in Assessment of metabolic variability and diversity present in leaf, peel and pulp tissue of diploid and triploid Musa spp.

Fig. 2. Heatmap highlighting significant differences of Fougamou (ABB) compared to Mbi egome (AAB). Colours show metabolite ratios for leaf, peel and pulp. Metabolites not detected in either variety are marked as ND. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedAug 2020View details →
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Fig. 5 in Assessment of metabolic variability and diversity present in leaf, peel and pulp tissue of diploid and triploid Musa spp.

Fig. 5. Heatmap of metabolites detected in pulp tissue. Metabolites and varieties were clustered (dendrograms) according to their similarity. Abundance of metabolites is indicated as high to low by a red to blue scale (see legend). Genome groups are displayed below the variety names. A more detailed version is available under Supplementary Fig. S5. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedAug 2020View details →
ClinicalTrials.gov32/100

Ultrasound Evaluation of the Myometrium Using the MUSA Terminology Comparison With Histology

ClinicalTrials.gov study NCT04990076. IPD Sharing: NO. Countries: 1. Publications: 2.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Adenomyosis in Fertile Women in MUSA Criteria

ClinicalTrials.gov study NCT06250569. IPD Sharing: NO. Countries: 1. Publications: 4.

closedIPD-NOFeb 2026View details →
zenodo28/100

Figure 2 from: Samarakoon BC, Phookamsak R, Wanasinghe DN, Chomnunti P, Hyde KD, Mckenzie EHC, Promputtha I, Xu J-C, Li Y-J (2020) Taxonomy and phylogenetic appraisal of Spegazzinia musae sp. nov. and S. deightonii (Didymosphaeriaceae, Pleosporales) on Musaceae from Thailand. MycoKeys 70: 19-37. https://doi.org/10.3897/mycokeys.70.52043

Figure 2 Spegazzinia deightonii (MFLU 19-2908) a–c fungal colonies on host surface d conidiophore mother cell of α conidia e–g α conidia i a developmental stage of β conidia h, k conidia l colonies on PDA after 28 days showing sporulation j, m–p β conidia. Scale bars: 500μm (a), 200μm (b), 50 μm (c), 20μm (e–h), 10μm (d, k, m–p), 5 μm (i, j).

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figure 1 from: Samarakoon BC, Phookamsak R, Wanasinghe DN, Chomnunti P, Hyde KD, Mckenzie EHC, Promputtha I, Xu J-C, Li Y-J (2020) Taxonomy and phylogenetic appraisal of Spegazzinia musae sp. nov. and S. deightonii (Didymosphaeriaceae, Pleosporales) on Musaceae from Thailand. MycoKeys 70: 19-37. https://doi.org/10.3897/mycokeys.70.52043

Figure 1 Maximum likelihood tree revealed by RAxML from an analysis of SSU, LSU and ITS and TEF1-α sequence data of selected genera of family Didymosphaeriaceae, showing the phylogenetic position of Spegazzinia musae (MFLUCC 20-0001) and S. deightonii (MFLUCC 20-0002). ML bootstrap supports (≥60 %) and Bayesian posterior probabilities (≥ 0.95 BYPP) are given above in the branches, respectively. The tree was rooted with Pleospora herbarum and Stemphylium botryosum (Pleosporaceae). Strains generated in this study are indicated in red-bold. Ex-type species are indicated in bold. The scale bar represents the expected number of nucleotide substitutions per site. A best scoring RAxML tree is shown with a final ML optimization likelihood value of -13516.66. The matrix had 795 distinct alignment patterns, with 33.60% of undetermined characters or gaps. Estimated base frequencies were: A = 0.239862, C = 0.245185, G = 0.277025, T = 0.237927; substitution rates AC = 1.626982, AG = 2.468452, AT = 1.211822, CG = 1.092437, CT = 6.295657, GT = 1.000000; proportion of invariable sites I = 0.484119; gamma distribution shape parameter α = 0.445929.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figure 3 from: Samarakoon BC, Phookamsak R, Wanasinghe DN, Chomnunti P, Hyde KD, Mckenzie EHC, Promputtha I, Xu J-C, Li Y-J (2020) Taxonomy and phylogenetic appraisal of Spegazzinia musae sp. nov. and S. deightonii (Didymosphaeriaceae, Pleosporales) on Musaceae from Thailand. MycoKeys 70: 19-37. https://doi.org/10.3897/mycokeys.70.52043

Figure 3 Spegazzinia musae (MFLU 19-2907, holotype) a–c fungal colonies on host surface d mature conidia e conidiophore of α conidia with the mother cell f, g α conidia h–q β conidia r colony on PDA after 28 days. Scale bars: 200 μm (a–c), 20 μm (d–g, j), 10 μm (h, i, k–q).

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figure 3 from: Samarakoon BC, Wanasinghe DN, Samarakoon MC, Phookamsak R, McKenzie EH.C, Chomnunti P, Hyde KD, Lumyong S, Karunarathna SC (2020) Multi-gene phylogenetic evidence suggests Dictyoarthrinium belongs in Didymosphaeriaceae (Pleosporales, Dothideomycetes) and Dictyoarthrinium musae sp. nov. on Musa from Thailand. MycoKeys 71: 101-118. https://doi.org/10.3897/mycokeys.71.55493

Figure 3 Dictyoarthrinium sacchari (MFLU 20-0439) a conidia on the host b developmental stage of terminal conidium attached to the conidiophore c–f Conidiophores and conidia (e, with distinct mother cell) g, h mature conidiophores with four-celled terminal conidium i conidiophore with two celled terminal conidium j developmental stages of conidia on conidiophore k colony on PDA after 21 days l–q conidia. Scale bars: a = 1000 μm (a); 20 μm (b, j); 50 μm (c–i); 5 μm (l–q).

opencc-by-4.0Aug 2020View details →
zenodo28/100

Figure 2 from: Samarakoon BC, Wanasinghe DN, Samarakoon MC, Phookamsak R, McKenzie EH.C, Chomnunti P, Hyde KD, Lumyong S, Karunarathna SC (2020) Multi-gene phylogenetic evidence suggests Dictyoarthrinium belongs in Didymosphaeriaceae (Pleosporales, Dothideomycetes) and Dictyoarthrinium musae sp. nov. on Musa from Thailand. MycoKeys 71: 101-118. https://doi.org/10.3897/mycokeys.71.55493

Figure 2 Dictyoarthrinium musae (MFLU 20-0437, holotype) a conidia on the host b conidiophore and conidia with conidiophore mother cell c–f conidia with conidiophores on stalk g developmental stage of an immature lateral conidium h four-celled terminal conidium i conidiophore j conidiophores and conidia with terminal conidium k, l conidiophores without terminal conidium m attachment of a mature lateral conidium n–q warted four-celled mature conidia r, s mature conidia that split at septa t colony on PDA after 21 days. Scale bars: 500 μm (a); 50 μm (b, c); 20 μm (d–g, i); 10 μm (h); 5 μm (j–s).

opencc-by-4.0Aug 2020View details →

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