Temporal diversity of Taraxacum kok-saghyz plants reveals high rubber yield phenotypes. Biodiversitas 17: 847-856. Taraxacum koksaghyz is a diploid, out-crossing, rubber-producing species under development as an alternative natural rubber crop. About 17,650 seed were obtained from progeny of 20 wild collected plants. New populations of plants were developed in Ohio from a random subsample of these seed, which were then open pollinated. In November 2011, these seed were direct seeded in outdoor shallow raised beds and in high tunnel deep raised beds. Plants were harvested from the outdoor beds from July 2012 to July 2013 to provide temporal phenotypic data as plants developed and overwintered. The high tunnel beds were harvested July 2013, and provided data on 11 individual accessions, and their progeny, and on the effect of winter bed heating. Plants were highly variable. Rubber concentration in root tissue was not directly correlated with root, shoot or plant size. Across all growing conditions and developmental stage, the highest rubber yields per plant were found in plants with large roots combined with a large rosette, and an above average rubber concentration. These parameters appeared to segregate independently, and rubber concentration was heritable. Interbreeding plants selected for large root, large rosette and then high rubber concentration, should rapidly move Taraxacum kok-saghyz towards domestication and commercialization.

Rubber dandelion (Taraxacum kok-saghyz, Rodin) is being developed as a temperate-zone source of rubber, but best agronomic practices must be determined before it can become a viable supplement to imported rubber produced from para rubber tree (Hevea brasiliensis, hevea) plantations located mostly in Southeast Asia. In our study, the effect of planting density and harvest time on yield was determined by transplanting 1.5-month-old greenhouse-produced plants at planting densities of 1.24, 2.47, 4.94, and 9.88 million plants/ha, randomized across four planting boxes with two densities per box (i.e., two planting areas at each density). Half of each planting area was selected randomly and hand-harvested after 6 months, and the remaining plants were hand-harvested after 1 year. Rubber yields per plant were greater after 1 year than after 6 months, but yields per unit area were similar as a result of the loss of half the plants during the severe 2013–14 Ohio winter. A maximum rubber yield of 960 kg dry rubber/ha was obtained from the 9.88 million-plants/ha planting density after 1 year, but root size was significantly decreased compared with lower densities, and appeared too small for mechanical harvest. A planting density between 2.47 and 4.94 million plants/ha may produce the optimal combination of root size and total rubber yield. Greater rubber concentrations, faster-growing plants, short-season germplasm, and in-field weed control are required before yields obtained in outdoor planting boxes can be matched or exceeded on farms, especially in a direct-seeded rubber dandelion crop.

Agrobacterium rhizogenes transformation is a more rapid method of obtaining transgenic and edited rubber dandelion (Taraxacum kok-saghyz) plants than Agrobacterium tumefaciens. The hairy root rol genes are present alongside transgenes after transformation, and they change the morphology of rubber dandelion significantly. Although these rol genes are useful visual markers indicating successful transformation of rubber dandelion, they modify the phenotype induced by the target transgenes and are ultimately detrimental to agronomic traits. Fortunately, the rol genes can be removed by conventional plant breeding because they segregate in progeny separately from the targeted transgenes. However, it is preferable to have preliminary identification of promising effects induced by transgenes or gene edits before rol gene removal so that only the best plants are used for breeding. Therefore, the goal of this research was to characterize rol– and rol+ plant morphology so that, in the future, rol+ transgene+ plants can be easily distinguished from rol+ transgene– plants. This requires that rol gene–induced morphological changes and simply assayed physiological traits are first characterized thoroughly so that transgene changes may be observed. Taproot formation is reduced or eliminated in rubber dandelion by rol genes, and rol-induced hairy roots are identifiable easily because they grow shallowly in potting soil, so only partial unearthing is needed. Both leaf and flower numbers are increased by rol genes, but leaves and flowers are smaller than in rubber dandelion wild type with longer stalks. The rosette doming phenotype caused by the induction of a large number of leaf primordia is obvious in rooted plants as young as 1 month old. Photosynthetic rates are reduced significantly in rol+ plants, although growth is not. An accurate description of the morphology of rubber dandelion after A. rhizogenes transformation may allow for initial selection of promising transformed plants before confirmation with polymerase chain reaction, by phenotypic comparison of plants expressing transgenes and the rol gene, with those only expressing the rol gene.