taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
03F34A591012FFA7FF51FD43789F5C33.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/6520357/files/figure.png	https://doi.org/10.5281/zenodo.6520357	FIGURE 3. Basidiobolus ranarnm (KUMCC 21-0467). a–c Appearance of colonies on PDA. d–e The branched hypha with zygospores stained by cotton blue reagent. f–g Zygospore with characteristic beak stained by cotton blue reagent. h Thick-walled zygospores stained by cotton blue reagent. i–k Producing meristospores stained by cotton blue reagent. Scale bars: d, e = 50 μm, f, g = 30 μm, h–k = 20 μm.	FIGURE 3. Basidiobolus ranarnm (KUMCC 21-0467). a–c Appearance of colonies on PDA. d–e The branched hypha with zygospores stained by cotton blue reagent. f–g Zygospore with characteristic beak stained by cotton blue reagent. h Thick-walled zygospores stained by cotton blue reagent. i–k Producing meristospores stained by cotton blue reagent. Scale bars: d, e = 50 μm, f, g = 30 μm, h–k = 20 μm.	2022-05-05	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.		Zenodo	biologists	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.			
03F34A591012FFA7FF51FD43789F5C33.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/6520355/files/figure.png	https://doi.org/10.5281/zenodo.6520355	FIGURE 2. Phylogram generated from maximum likelihood analysis based on a combined LSU, ITS, rpb2 and mtSSU sequence datasets. Related sequences were taken from Gryganskyi et al. (2013), Nie et al. (2020) and Al-Hatmi et al. (2021). The 14 strains are included in the combined gene analyses; 3258 total characters including gaps (LSU: 1–1021 bp, ITS: 1022–1745 bp, rpb2: 1746–2590 bp, mtSSU: 2591–3258 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 -10673.579273 (ln).All free model parameters were estimated using the RAxML model, with 586 distinct alignment patterns and 21.73% undetermined characters or gaps. Estimated base frequencies were as follows:A = 0.280858, C = 0.195362, G = 0.257773, T = 0.266007, with substitution rates AC = 1.709550, AG = 4.063199, AT = 2.099405, CG = 1.130856, CT = 8.827188, GT = 1.000000. The gamma distribution shape parameter alpha = 0.109274 and the Tree-Length = 4.770478. The final average standard deviation of split frequencies at the end of total MCMC generations were calculated as 0.009712 in BI analysis. The species determined in this study are indicated in red. Bootstrap values equal to or greater than 70% (ML, left) and Bayesian posterior probabilities (BI, right) equal to or greater than 0.90 are given at the nodes. Hyphens (-) represent support values less than 70% in ML/0.90 in BI.	FIGURE 2. Phylogram generated from maximum likelihood analysis based on a combined LSU, ITS, rpb2 and mtSSU sequence datasets. Related sequences were taken from Gryganskyi et al. (2013), Nie et al. (2020) and Al-Hatmi et al. (2021). The 14 strains are included in the combined gene analyses; 3258 total characters including gaps (LSU: 1–1021 bp, ITS: 1022–1745 bp, rpb2: 1746–2590 bp, mtSSU: 2591–3258 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 -10673.579273 (ln).All free model parameters were estimated using the RAxML model, with 586 distinct alignment patterns and 21.73% undetermined characters or gaps. Estimated base frequencies were as follows:A = 0.280858, C = 0.195362, G = 0.257773, T = 0.266007, with substitution rates AC = 1.709550, AG = 4.063199, AT = 2.099405, CG = 1.130856, CT = 8.827188, GT = 1.000000. The gamma distribution shape parameter alpha = 0.109274 and the Tree-Length = 4.770478. The final average standard deviation of split frequencies at the end of total MCMC generations were calculated as 0.009712 in BI analysis. The species determined in this study are indicated in red. Bootstrap values equal to or greater than 70% (ML, left) and Bayesian posterior probabilities (BI, right) equal to or greater than 0.90 are given at the nodes. Hyphens (-) represent support values less than 70% in ML/0.90 in BI.	2022-05-05	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.		Zenodo	biologists	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.			
03F34A59101FFFAAFF51FCCB79D853D5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/6520361/files/figure.png	https://doi.org/10.5281/zenodo.6520361	FIGURE 5. Beauveria bassiana (KUMCC 21-0468).aAppearance of fungal colonies on PDA.b Close-up of fungal colonies. c Mycelium with conidia. d Mycelium mass stained by cotton blue reagent. e Conidia connected with conidiogenous cells and stained by cotton blue reagent. f A conidophore. g A branched mycelium stained by congo red reagent. h Minus and plus mycelium stained by congo red reagent. i Conidia stained by congo red reagent. j Conidia stained by cotton blue reagent. Scale bars: d = 50 μm, c, e = 30 μm, g, h = 10 μm, f, i, j = 5 μm.	FIGURE 5. Beauveria bassiana (KUMCC 21-0468).aAppearance of fungal colonies on PDA.b Close-up of fungal colonies. c Mycelium with conidia. d Mycelium mass stained by cotton blue reagent. e Conidia connected with conidiogenous cells and stained by cotton blue reagent. f A conidophore. g A branched mycelium stained by congo red reagent. h Minus and plus mycelium stained by congo red reagent. i Conidia stained by congo red reagent. j Conidia stained by cotton blue reagent. Scale bars: d = 50 μm, c, e = 30 μm, g, h = 10 μm, f, i, j = 5 μm.	2022-05-05	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.		Zenodo	biologists	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.			
03F34A59101FFFAAFF51FCCB79D853D5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/6520359/files/figure.png	https://doi.org/10.5281/zenodo.6520359	FIGURE 4. Phylogram generated from maximum likelihood analysis based on a combined ITS, rpb1, rpb2, tef1-α and Bloc sequence datasets. Related sequences were taken from Chen et al. (2018) and Khonsanit et al. (2020). A total of 81 strains are included in the combined gene analyses; 5090 total characters including gaps (ITS: 1–566 bp, rpb1: 567–1307 bp, rpb2: 1308–2430 bp, tef1-α: 2431–3429 bp, Bloc: 3430-5090 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 -29154.321884 (ln). All free model parameters were estimated using the RAxML model, with 1867 distinct alignment patterns and 15.05% of undetermined characters or gaps. Estimated base frequencies were as follows: A = 0.242248, C = 0.283924, G = 0.257262, T = 0.216566, with substitution rates AC = 0.928484, AG = 3.845624, AT = 0.649405, CG = 0.874887, CT = 4.792288, GT = 1.000000. The gamma distribution shape parameter alpha = 0.712530 and the Tree-Length = 1.618181. The final average standard deviation of split frequencies at the end of total MCMC generations calculated as 0.009746 in BI analysis. The species determined in this study are indicated in red.Bootstrap values equal to or greater than 70% (ML, left) and Bayesian posterior probabilities (BI, right) equal to or greater than 0.95 are given at the nodes. Hyphens (-) represent support values less than 70% in ML/0.95 in BI.	FIGURE 4. Phylogram generated from maximum likelihood analysis based on a combined ITS, rpb1, rpb2, tef1-α and Bloc sequence datasets. Related sequences were taken from Chen et al. (2018) and Khonsanit et al. (2020). A total of 81 strains are included in the combined gene analyses; 5090 total characters including gaps (ITS: 1–566 bp, rpb1: 567–1307 bp, rpb2: 1308–2430 bp, tef1-α: 2431–3429 bp, Bloc: 3430-5090 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 -29154.321884 (ln). All free model parameters were estimated using the RAxML model, with 1867 distinct alignment patterns and 15.05% of undetermined characters or gaps. Estimated base frequencies were as follows: A = 0.242248, C = 0.283924, G = 0.257262, T = 0.216566, with substitution rates AC = 0.928484, AG = 3.845624, AT = 0.649405, CG = 0.874887, CT = 4.792288, GT = 1.000000. The gamma distribution shape parameter alpha = 0.712530 and the Tree-Length = 1.618181. The final average standard deviation of split frequencies at the end of total MCMC generations calculated as 0.009746 in BI analysis. The species determined in this study are indicated in red.Bootstrap values equal to or greater than 70% (ML, left) and Bayesian posterior probabilities (BI, right) equal to or greater than 0.95 are given at the nodes. Hyphens (-) represent support values less than 70% in ML/0.95 in BI.	2022-05-05	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.		Zenodo	biologists	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.			
03F34A59101BFFAEFF51FCEF7D2752B5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/6520365/files/figure.png	https://doi.org/10.5281/zenodo.6520365	FIGURE 7. Colletotrichum jiangxiense (KUMCC 21-0466). a, b Colonies on PDA. c Hyphae. d Hyphae stained by cotton blue reagent. e, f Conidophores connected with conidia (f: stained by congo red reagent). g–i Conidia (g: stained by cotton blue reagent). Scale bars: c, d = 20 μm, e–i = 10 μm.	FIGURE 7. Colletotrichum jiangxiense (KUMCC 21-0466). a, b Colonies on PDA. c Hyphae. d Hyphae stained by cotton blue reagent. e, f Conidophores connected with conidia (f: stained by congo red reagent). g–i Conidia (g: stained by cotton blue reagent). Scale bars: c, d = 20 μm, e–i = 10 μm.	2022-05-05	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.		Zenodo	biologists	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.			
03F34A59101BFFAEFF51FCEF7D2752B5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/6520363/files/figure.png	https://doi.org/10.5281/zenodo.6520363	FIGURE 6. Phylogram generated from maximum likelihood analysis based on a combined ITS, HIS, CAL, ACT, tub2 and GPDH sequence datasets. Related sequences were taken from Diao et al. (2017) and Chaiwan et al. (2021). The 52 strains are included in the combined gene analyses, 2882 total characters including gaps (ITS: 1–579 bp, HIS: 580–874 bp, CAL: 875–1610 bp, ACT: 1611–1888 bp, tub2: 1889–2602 bp, GPDH: 2603–2882). 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 -14018.222367 (ln). All free model parameters were estimated using the RAxML model, with 1867 distinct alignment patterns and 15.05% of undetermined characters or gaps. Estimated base frequencies were as follows: A = 0.227166, C = 0.283924, G = 0.257262, T = 0.216566, with substitution rates AC = 1.035930, AG = 0.298823, AT = 0.248992, CG = 0.225019, CT = 4.115498, GT = 1.000000. The gamma distribution shape parameter alpha = 0.904631 and the Tree- Length = 0.821909. The final average standard deviation of split frequencies at the end of total MCMC generations calculated as 0.009613 in BI analysis. The species determined in this study are indicated in red. Bootstrap values equal to or greater than 70% (ML, left) and Bayesian posterior probabilities (BI, right) equal to or greater than 0.95 are given at the nodes. Hyphens (-) represent support values less than 70% in ML/0.95 in BI.	FIGURE 6. Phylogram generated from maximum likelihood analysis based on a combined ITS, HIS, CAL, ACT, tub2 and GPDH sequence datasets. Related sequences were taken from Diao et al. (2017) and Chaiwan et al. (2021). The 52 strains are included in the combined gene analyses, 2882 total characters including gaps (ITS: 1–579 bp, HIS: 580–874 bp, CAL: 875–1610 bp, ACT: 1611–1888 bp, tub2: 1889–2602 bp, GPDH: 2603–2882). 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 -14018.222367 (ln). All free model parameters were estimated using the RAxML model, with 1867 distinct alignment patterns and 15.05% of undetermined characters or gaps. Estimated base frequencies were as follows: A = 0.227166, C = 0.283924, G = 0.257262, T = 0.216566, with substitution rates AC = 1.035930, AG = 0.298823, AT = 0.248992, CG = 0.225019, CT = 4.115498, GT = 1.000000. The gamma distribution shape parameter alpha = 0.904631 and the Tree- Length = 0.821909. The final average standard deviation of split frequencies at the end of total MCMC generations calculated as 0.009613 in BI analysis. The species determined in this study are indicated in red. Bootstrap values equal to or greater than 70% (ML, left) and Bayesian posterior probabilities (BI, right) equal to or greater than 0.95 are given at the nodes. Hyphens (-) represent support values less than 70% in ML/0.95 in BI.	2022-05-05	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.		Zenodo	biologists	Yang, Erfu;Tibpromma, Saowaluck;Dai, Dongqin;Promputtha, Itthayakorn;Mortimer, Peter E.;Karunarathna, Samantha C.			
