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633 results for “Kd”
Figure 7 from: Prathapan KD, Poorani J, Amritha Kumari S, Anuradha C, Padmanaban B, Thanigairaj R (2019) Species composition and diagnoses of leaf- and fruit-scarring beetles (Coleoptera, Chrysomelidae) infesting bananas and plantains (Zingiberales, Musaceae) in the Indian subcontinent. Deutsche Entomologische Zeitschrift 66(2): 179-202. https://doi.org/10.3897/dez.66.47447
Figure 7 Damage caused by B. subcostata (Jacoby) on banana. a. Leaf whorl showing scarring damage; b. Scars on spindle leaf; c. Scars on leaf; d, e. Scarring on leaf petiole; f. Flower damage; g. Bract damage; h–i. Damage on young fruits and emerging bunch; j–l. Fruit damage.
Figure 1 from: Tennakoon DS, Thambugala KM, Jeewon R, Hongsanan S, Kuo C-H, Hyde KD (2019) Additions to Chaetothyriaceae (Chaetothyriales): Longihyalospora gen. nov. and Ceramothyrium longivolcaniforme, a new host record from decaying leaves of Ficus ampelas. MycoKeys 61: 91-109. https://doi.org/10.3897/mycokeys.61.47056
Figure 1 RAxML tree based on a combined dataset of ITS, LSU and SSU partial sequences of 45 taxa. Bootstrap support values for maximum likelihood (ML and, maximum parsimony (MP) values higher than 60 % and Bayesian posterior probabilities (BYPP) greater than 0.90 are given above each branch respectively. The new isolates are in red. Ex-type strains are in bold. The tree is rooted by Leptoxyphium fumago (CBS 123.26) and L. madagascariense (CBS 124766).
Figure 3 from: Tennakoon DS, Thambugala KM, Jeewon R, Hongsanan S, Kuo C-H, Hyde KD (2019) Additions to Chaetothyriaceae (Chaetothyriales): Longihyalospora gen. nov. and Ceramothyrium longivolcaniforme, a new host record from decaying leaves of Ficus ampelas. MycoKeys 61: 91-109. https://doi.org/10.3897/mycokeys.61.47056
Figure 3 Longihyalospora ampeli (MFLU 19-0824, holotype). a Host leaf b appearance of colony (black spots) on leaf c ring of setae around the pellicle d mycelial pellicle with setae e mycelial pellicle cells f, g vertical section through ascoma h section of peridium i–m asci n–r ascospores s ascospore stained in Indian ink showing a mucilaginous sheath. Scale bars: 100 µm (c), 75 µm (d), 20 µm (e, f), 50 µm (g), 10 µm (h), 50 µm (i–m), 20 µm (n–s).
Figure 2 from: Tennakoon DS, Thambugala KM, Jeewon R, Hongsanan S, Kuo C-H, Hyde KD (2019) Additions to Chaetothyriaceae (Chaetothyriales): Longihyalospora gen. nov. and Ceramothyrium longivolcaniforme, a new host record from decaying leaves of Ficus ampelas. MycoKeys 61: 91-109. https://doi.org/10.3897/mycokeys.61.47056
Figure 2 Ceramothyrium longivolcaniforme (MFLU19-0823, new host record). a, b Appearance of colony (black spots) on host leaf c mycelial pellicle d vertical section through ascoma e section of peridium f–i asci j–m ascospores n ascospore stained in Indian ink showing mucilaginous sheath o germinating ascospore p, q colony from above and below. Scale bars: 50 µm (d), 10 µm (e), 20 µm (f–i), 10 µm (j–o).
Figure 2 from: Zhang Q, Yang Z-F, Cheng W, Wijayawardene NN, Hyde KD, Chen Z, Wang Y (2020) Diseases of Cymbopogon citratus (Poaceae) in China: Curvularia nanningensis sp. nov. MycoKeys 63: 49-67. https://doi.org/10.3897/mycokeys.63.49264
Figure 2 Maximum Parsimony (MP) analysis of Curvularia pathogens in China, India and Pakistan based on ITS sequences. Alternaria alternata (taxon:5599) was used as outgroup taxon. Bootstrap values (≥ 50%) of the MP method are shown near the nodes.
Figure 1 from: Zhang Q, Yang Z-F, Cheng W, Wijayawardene NN, Hyde KD, Chen Z, Wang Y (2020) Diseases of Cymbopogon citratus (Poaceae) in China: Curvularia nanningensis sp. nov. MycoKeys 63: 49-67. https://doi.org/10.3897/mycokeys.63.49264
Figure 1 Maximum Parsimony (MP) topology of Curvularia generated from a combination of ITS, GAPDH and tef1 sequences. Bipolaris maydis (CBS 136.29) and B. drechsleri (MUS0028) were used as outgroup taxa. MP and ML above 50% and BPP values above 0.90 were placed close to topological nodes and separated by "/". The bootstrap values below 50% and BPP values below 0.90 were labelled with "-". Our main research clade was labelled with green colour.
Supplementary material 1 from: Zhang Q, Yang Z-F, Cheng W, Wijayawardene NN, Hyde KD, Chen Z, Wang Y (2020) Diseases of Cymbopogon citratus (Poaceae) in China: Curvularia nanningensis sp. nov. MycoKeys 63: 49-67. https://doi.org/10.3897/mycokeys.63.49264
: Data type: (measurement/occurrence/multimedia/etc.)
Figure 4 from: Zhang Q, Yang Z-F, Cheng W, Wijayawardene NN, Hyde KD, Chen Z, Wang Y (2020) Diseases of Cymbopogon citratus (Poaceae) in China: Curvularia nanningensis sp. nov. MycoKeys 63: 49-67. https://doi.org/10.3897/mycokeys.63.49264
Figure 4 Pathogen inoculation and symptom (4 days). ACymbopogon citratus inoculated and disease symptom B inoculation point and disease symptom C control D detached experiment. Left. Control. Right. Inoculation point and disease symptoms.
Figure 3 from: Zhang Q, Yang Z-F, Cheng W, Wijayawardene NN, Hyde KD, Chen Z, Wang Y (2020) Diseases of Cymbopogon citratus (Poaceae) in China: Curvularia nanningensis sp. nov. MycoKeys 63: 49-67. https://doi.org/10.3897/mycokeys.63.49264
Figure 3 Curvularia nanningensis (GUCC11005, holotype) A, B diseased symptom C colony on PDA from above D colony on PDA from below E−G conidia and conidiophores H−I conidia. Scale bars: 50 μm (E), 20 μm (F), 10 μm (G−I).
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).
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.
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).
Figure 6 from: Tennakoon DS, Thambugala KM, Wanasinghe DN, Gentekaki E, Promputtha I, Kuo C-H, Hyde KD (2020) Additions to Phaeosphaeriaceae (Pleosporales): Elongaticollum gen. nov., Ophiosphaerella taiwanensis sp. nov., Phaeosphaeriopsis beaucarneae sp. nov. and a new host record of Neosetophoma poaceicola from Musaceae. MycoKeys 70: 59-88. https://doi.org/10.3897/mycokeys.70.53674
Figure 6 Neosetophoma poaceicola (MFLU 18–2597, new host record) a appearance of ascomata on host b close up of ascomata c vertical section through ascoma d peridium e pseudoparaphyses f–h asci i–k ascospores l germinated ascospore in PDAm colony from above n colony from below. Scale bars: 50 µm (c), 20 µm (d), 30 µm (e–h), 15 µm (i–l).
Figure 5 from: Tennakoon DS, Thambugala KM, Wanasinghe DN, Gentekaki E, Promputtha I, Kuo C-H, Hyde KD (2020) Additions to Phaeosphaeriaceae (Pleosporales): Elongaticollum gen. nov., Ophiosphaerella taiwanensis sp. nov., Phaeosphaeriopsis beaucarneae sp. nov. and a new host record of Neosetophoma poaceicola from Musaceae. MycoKeys 70: 59-88. https://doi.org/10.3897/mycokeys.70.53674
Figure 5 Phaeosphaeriopsis beaucarneae (MFLU 18-2586, paratype) a appearance of conidiomata on host b close up of conidiomata c vertical section through conidioma d conidiomatal wall e, f conidiogenous cells and developing conidia g–i conidia j germinated conidium in PDAk colony from above l colony from below. Scale bars: 100 µm (c), 20 µm (d), 3 µm (e, f), 5 µm (g–j).
Figure 4 from: Tennakoon DS, Thambugala KM, Wanasinghe DN, Gentekaki E, Promputtha I, Kuo C-H, Hyde KD (2020) Additions to Phaeosphaeriaceae (Pleosporales): Elongaticollum gen. nov., Ophiosphaerella taiwanensis sp. nov., Phaeosphaeriopsis beaucarneae sp. nov. and a new host record of Neosetophoma poaceicola from Musaceae. MycoKeys 70: 59-88. https://doi.org/10.3897/mycokeys.70.53674
Figure 4 Phaeosphaeriopsis beaucarneae (MFLU 18-2586, holotype) a appearance of ascomata on host b close up of ascoma c vertical section through ascoma d peridium e pseudoparaphyses f–i asci j–n ascospores o germinated ascospore in PDAp colony from above q colony from below. Scale bars: 100 µm (c), 15 µm (d), 50 µm (e–i), 10 µm (j–o).
Figure 2 from: Tennakoon DS, Thambugala KM, Wanasinghe DN, Gentekaki E, Promputtha I, Kuo C-H, Hyde KD (2020) Additions to Phaeosphaeriaceae (Pleosporales): Elongaticollum gen. nov., Ophiosphaerella taiwanensis sp. nov., Phaeosphaeriopsis beaucarneae sp. nov. and a new host record of Neosetophoma poaceicola from Musaceae. MycoKeys 70: 59-88. https://doi.org/10.3897/mycokeys.70.53674
Figure 2 Elongaticollum hedychii (MFLU 18-2542, holotype) a specimen b appearance of conidiomata on host c close up of conidiomata on host d vertical section through conidioma e, f squash mount of conidioma g conidioma wall h, i elongated conidiomatal necks j conidiogenous cells k conidia l, m germinated conidia n colony from below o colony from above p, q pycnidia formed on PDA. Scale bars: 100 µm (c), 50 µm (d–h), 10 µm (g), 30 µm (i), 3 µm (j–m), 100 µm (p, q).
Figure 1 from: Tennakoon DS, Thambugala KM, Wanasinghe DN, Gentekaki E, Promputtha I, Kuo C-H, Hyde KD (2020) Additions to Phaeosphaeriaceae (Pleosporales): Elongaticollum gen. nov., Ophiosphaerella taiwanensis sp. nov., Phaeosphaeriopsis beaucarneae sp. nov. and a new host record of Neosetophoma poaceicola from Musaceae. MycoKeys 70: 59-88. https://doi.org/10.3897/mycokeys.70.53674
Figure 1 RAxML tree inferred from combined dataset of ITS, LSU, SSU and tef1-α partial sequences of 168 strains of Phaeosphaeriaceae. Bootstrap support values for maximum likelihood (ML), maximum parsimony (MP) values ≥70%, and Bayesian posterior probabilities (BYPP) ≥0.95 are given above each branch respectively. The new species are highlighted in red, and the new record in green. Ex-type strains are in bold. The tree is rooted by Leptosphaeria doliolum (CBS 505.75) and Paraleptosphaeria dryadis (CBS 643.86).
Figure 3 from: Tennakoon DS, Thambugala KM, Wanasinghe DN, Gentekaki E, Promputtha I, Kuo C-H, Hyde KD (2020) Additions to Phaeosphaeriaceae (Pleosporales): Elongaticollum gen. nov., Ophiosphaerella taiwanensis sp. nov., Phaeosphaeriopsis beaucarneae sp. nov. and a new host record of Neosetophoma poaceicola from Musaceae. MycoKeys 70: 59-88. https://doi.org/10.3897/mycokeys.70.53674
Figure 3 Ophiosphaerella taiwanensis (MFLU 18-2534, holotype) a, b appearance of ascomata on host c close-up of ascomata d vertical section through ascoma e apex of ascoma f peridium g pseudoparaphyses h–j asci k, l ascospores m germinated ascospore in PDAn colony from above o colony from below. Scale bars: 100 µm (d, e), 15 µm (f), 50 µm (g–m).
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).
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).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.