Financial support: INTA project number 1837.Keywords: colchicine, flow cytometry, ornamental plants, Scrophulariaceae, tetraploid.Abbreviations: BAP: 6-benzyl amino purine DMSO: dimethylsulfoxide MS: Murashige and Skoog (1962) The commercial value of Bacopa monnieri, a widespread herbaceous plant in Argentina, can be substantially improved increasing its flower size by chromosome doubling with colchicine. MS supplemented with 0.25 mg/L of 6-benzylaminopurine proved to be an appropriate medium for the in vitro multiplication of nodal segments of B. monnieri. Polyploidization was achieved submerging nodal segments during 24 or 48 hrs in colchicine solution 0.001 and 0.01% P/V, in 1% DMSO. Segments submerged in water and in DMSO 1% aqueous solution were used as controls. DNA contents from recovered plants was measured and characterized and their phenotype described. Two tetraploid plants originated from independent events were detected. These plants showed significant differences in size and colour both in leaves and flowers compared to untreated controls.

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Calibrachoa (Solanaceae) is a plant genus typical of open environments that occurs in both the Pampas and the high-altitude grasslands of southern Brazil (Fregonezi et al. 2012). Calibrachoas (mini petunias) are hybrids developed from native germplasm, with increasing importance in the ornamental plant market. During October 2019, basal rot was observed in plants of C. hybrida cv. INTA 06575 grown in a propagation greenhouse in Hurlingham, Buenos Aires. Those symptoms caused the darkening and withering of the leaves (incidence of 10 %). White mycelial mats containing sclerotia of 2 to 8 mm in diameter were evident on the base of the wilted plants and the nearby soil surface. Pieces of symptomatic stem tissues were surface-disinfested in ethanol 70% for 1 min, sodium hypochlorite (2 g Cl/L) for 1 min, washed with distilled water for 1 min, and placed on potato dextrose agar (PDA) plates. The plates were incubated in the dark for 5 days at 23°C and individual colonies were transferred to new plates of PDA to obtain pure cultures. The colonies developed white cottony mycelium, and a ring of large black sclerotia at the periphery of the plates. No teleomorph was observed. Based on the morphology of the colony, sclerotia, and microscopic observations, the pathogen was identified as Sclerotinia sclerotiorum (Lib.) de Bary (Mordue and Holliday 1976). A representative isolate was deposited in the Entomopathogenic Fungal Culture Collection of Argentina, CEPAVE as CEP 785. Genomic DNA was extracted and the internal transcribed spacer (ITS) region of rDNA was amplified with the primers ITS1/ITS4 (White et al. 1990). The resulting sequence was deposited in GenBank (Accession No. MT177216) and the BLASTn search showed 100 % of identity with those of S. sclerotiorum (ex. MG931017, KX781301). The pathogenicity of the isolate was confirmed by placing plugs of 10 mm2 obtained from a 7-day-old culture grown on PDA,on the stem bases of 12 healthy potted calibrachoas 2 months old. Those segments were wrapped with moistened sterilized cotton (Choi et al. 2017). Four plants with sterile PDA plugs served as controls. Each plant was placed inside a polyethylene bag, and all of them were kept in a growth chamber at 20°C. All the inoculated plants had their leaves discolored after five days, and wilted after thirteen days. Sclerotinia sclerotiorum was consistently re-isolated from rotten stem bases, thus fulfilling Koch’s postulates. Control plants did not develop symptoms. To our knowledge, this is the first report of S. sclerotiorum causing basal rot on Calibrachoa hybrida (Farr and Rossman 2020) in Argentina, and in the world.