The invention provides seed and plants of the bean line designated SV0579GG. The invention thus relates to the plants, seeds and tissue cultures of bean line SV0579GG, and to methods for producing a bean plant produced by crossing a plant of bean line SV0579GG with itself or with another bean plant, such as a plant of another line. The invention further relates to seeds and plants produced by such crossing. The invention further relates to parts of a plant of bean line SV0579GG, including the pods and gametes of such plants.

The cotton variety FM 1911GLT is disclosed. The invention relates to seeds, plants, plant cells, plant tissue, harvested products and cotton lint as well as to hybrid cotton plants and seeds obtained by repeatedly crossing plants of variety FM 1911GLT with other plants. The invention also relates to plants and varieties produced by the method of essential derivation from plants of FM 1911GLT and to plants of FM 1911GLT reproduced by vegetative methods, including but not limited to tissue culture of regenerable cells or tissue from FM 1911GLT.

The invention relates to a dominant mutation in the TDM gene leading to the production of 2n gametes in plants, to the plants comprising said mutation, and to their use in plant breeding. The invention relates also to plants in which the dominant mutation in the TDM gene is combined with the inactivation of a gene involved in meiotic recombination in plants and a gene involved in the monopolar orientation of the kinetochores during meiosis. These plants which produce apomeiotic gametes are also useful in plant breeding.

The present invention relates to a hybrid Swiss chard seed designated 69-104 RZ. The present invention also relates to a Swiss chard plant produced by growing the 69-104 RZ seed, which plant exhibits a combination of traits including green leaves with a reddish purple petiole and midrib, slow growing, resistance to downy mildew (Peronospora farinosa f sp. betae), a dark to very dark green leaf coloring and strongly blistered leaf blades. The invention further relates to methods for producing the Swiss chard cultivar, represented by hybrid Swiss chard variety 69-104 RZ.

The present invention relates to a Diplotaxis tenuifolia seed designated 89-001 RZ, which exhibits a combination of traits including downy mildew resistance, medium to dark grey green leaves, high leaf thickness and very narrow primary lobes. The present invention also relates to a Diplotaxis tenuifolia plant produced by growing the 89-001 RZ seed. The invention further relates to methods for producing the wild rocket cultivar, represented by wild rocket variety 89-001 RZ.

The present invention relates generally to an artificial plant seed and to its use for plant propagation, in particular, for the propagation of cannabis plants.

Disclosed herein are methods of producing one or more cannabinoid compounds, expanding cells that produce the compounds, cannabinoid compounds produced by the methods, pharmaceutical compositions comprising the cannabinoid compounds, and methods of producing and utilizing the compounds and compositions.

Disclosed herein are methods of producing one or more cannabinoid compounds, expanding cells that produce the compounds, cannabinoid compounds produced by the methods, pharmaceutical compositions comprising the cannabinoid compounds, and methods of producing and utilizing the compounds and compositions.

Methods for obtaining genetic material from plant embryos while preserving their viability are provided. In the methods, preservation of viability may be maintained by suspending the embryos in an aqueous solution surrounded by an oil matrix. Genetic material may be obtained from an aliquot of the aqueous solution and may be used directly for molecular analysis, or whole genome amplification may be performed prior to molecular analysis.

Methods for obtaining genetic material from plant embryos while preserving their viability are provided. In the methods, preservation of viability may be maintained by suspending the embryos in an aqueous solution surrounded by an oil matrix. Genetic material may be obtained from an aliquot of the aqueous solution and may be used directly for molecular analysis, or whole genome amplification may be performed prior to molecular analysis.