This dataset contains the digitized treatments in Plazi based on the original journal article Zhang, Miao, Zhang, Xiao-Hui, Shi, Shi, Chen, Bing-Hua (2023): Lithocarpus dahuensis (Fagaceae), a new species from Fujian Province based on morphology and genomic data. PhytoKeys 222: 1-18, DOI: http://dx.doi.org/10.3897/phytokeys.222.99370, URL: http://dx.doi.org/10.3897/phytokeys.222.99370

This dataset contains the digitized treatments in Plazi based on the original journal article Zhang, Miao, Zhang, Xiao-Hui, Ge, Chang-Li, Chen, Bing-Hua (2022): Terniopsis yongtaiensis (Podostemaceae), a new species from South East China based on morphological and genomic data. PhytoKeys 194: 105-122, DOI: http://dx.doi.org/10.3897/phytokeys.194.83080, URL: http://dx.doi.org/10.3897/phytokeys.194.83080

This dataset contains the digitized treatments in Plazi based on the original journal article Chen, Bing-Hua, Zhang, Miao, Zhao, Kai, Zhang, Xiao-Hui, Ge, Chang-Li (2022): Polypleurum chinense (Podostemaceae), a new species from Fujian, China, based on morphological and genomic evidence. PhytoKeys 199: 167-186, DOI: http://dx.doi.org/10.3897/phytokeys.199.85679, URL: http://dx.doi.org/10.3897/phytokeys.199.85679

This dataset contains the digitized treatments in Plazi based on the original journal article Zhang, Miao, Zhang, Xiao-Hui, Ge, Chang-Li, Chen, Bing-Hua (2022): Danxiaorchis mangdangshanensis (Orchidaceae, Epidendroideae), a new species from central Fujian Province based on morphological and genomic data. PhytoKeys 212: 37-55, DOI: http://dx.doi.org/10.3897/phytokeys.212.91534, URL: http://dx.doi.org/10.3897/phytokeys.212.91534

Figure S1. The number and coverage of RAD-tags for G-type, P-type and each F2 individual of Barbarea vulgaris. The x-axis indicates the plant accession including G-type, P-type and each of the F2 individuals; the y-axis indicates the number of RAD-tags (a) and the coverage (b). Figure S2. Characteristics of the glucosinolate profiles in F2 offspring from a cross between P-type and G-type B. vulgaris. a. Glucosinolates from each of the two biosynthetic families, tryptophan (Trp) derived and phenylalanine (Phe) derived, showed little correlation. b. Three large, rather well defined groups of progeny plants could be recognized from the balance of the glucosinolate epimers BAR and EBAR. For the inserted hypothetic genotypes, see Discussion. The question marks indicate that the genotypes may be overly simplified, due to additional genes influencing the glucosinolate profile. In addition, a further fine structure in the group SHO RHO is evident, with one group (the upper) relatively higher in EBAR than the other. c. A plot of NAS levels as a function of the sum of its two hydroxyl derivatives BAR and EBAR revealed a small deviating group of â NAS-formâ progeny plants, characterized by very low levels of both epimeric glucobarbarins (BAR and EBAR), resulting in accumulation of the apparent biosynthetic precursor, NAS. Reasons for the very low number of apparent sho rho plants are discussed in Discussion. d. Levels of the 4-substituted indole glucosinolate 4mIM were essentially not correlated with the precursor IM, suggesting the substitution to be specifically regulated, in agreement with identification of a major QTL for 4mIM (ZIP 238 kb)

Figure S1. The number and coverage of RAD-tags for G-type, P-type and each F2 individual of Barbarea vulgaris. The x-axis indicates the plant accession including G-type, P-type and each of the F2 individuals; the y-axis indicates the number of RAD-tags (a) and the coverage (b). Figure S2. Characteristics of the glucosinolate profiles in F2 offspring from a cross between P-type and G-type B. vulgaris. a. Glucosinolates from each of the two biosynthetic families, tryptophan (Trp) derived and phenylalanine (Phe) derived, showed little correlation. b. Three large, rather well defined groups of progeny plants could be recognized from the balance of the glucosinolate epimers BAR and EBAR. For the inserted hypothetic genotypes, see Discussion. The question marks indicate that the genotypes may be overly simplified, due to additional genes influencing the glucosinolate profile. In addition, a further fine structure in the group SHO RHO is evident, with one group (the upper) relatively higher in EBAR than the other. c. A plot of NAS levels as a function of the sum of its two hydroxyl derivatives BAR and EBAR revealed a small deviating group of â NAS-formâ progeny plants, characterized by very low levels of both epimeric glucobarbarins (BAR and EBAR), resulting in accumulation of the apparent biosynthetic precursor, NAS. Reasons for the very low number of apparent sho rho plants are discussed in Discussion. d. Levels of the 4-substituted indole glucosinolate 4mIM were essentially not correlated with the precursor IM, suggesting the substitution to be specifically regulated, in agreement with identification of a major QTL for 4mIM (ZIP 238 kb)

Table S1. Anchoring of sequenced contigs of G-type Barbarea vulgaris to the eight linkage groups. Table S2. Comparison of anchored contig information between this and the best previous Barbarea vulgaris genome assembly. Table S3. The trichome density, color, maximum leaf length and width, and glucosinolate content in the leaves of each individual of the F2 population of Barbarea vulgaris (ZIP 1442 kb)

Table S1. Anchoring of sequenced contigs of G-type Barbarea vulgaris to the eight linkage groups. Table S2. Comparison of anchored contig information between this and the best previous Barbarea vulgaris genome assembly. Table S3. The trichome density, color, maximum leaf length and width, and glucosinolate content in the leaves of each individual of the F2 population of Barbarea vulgaris (ZIP 1442 kb)