variety Hybridisation of
Streptocarpus is conceptually very simple. The pollen of one plant (therefore the father) is placed onto the tip of the stigma of another plant (the mother). To prevent unwanted self-pollination of the mother plant, carefully remove its
anthers beforehand. To help prevent unwanted cross-pollination, cover the newly fertilized stigma with a small plastic bag. If fertilization was successful, the seed pod will start to elongate within a few days. As the pod grows, it will start showing its namesake twisted form. Once the pod is mature, it will turn brown, dry off, and split open along the spiralled seams to release the seeds. Another method that is used to create hybrids is to use radiation or chemicals to alter the genes. For example,
irradiation may be used (e.g. xrays, gamma rays) to induce
mutations that may give rise to plants with new characteristics. Another example is the use of
colchicine to induce
polyploidy (multiplying number of chromosomes) in plants, also to introduce new traits. Over the years, numerous hybrids have been produced.
S. rexii was used in many of the early hybrids, and its form is one that we most recognize in modern-day hybrids. But more recent hybrids may contain the genes of other species or hybrids. When making a cross, hybridizers keep in mind which traits they wish to bring out or improve in the progeny. Much hybridizing work has been done to produce modern hybrids with an increased range of flower colours and forms, leaf variations, increased flowering periods, and more recently to introduce scent. Thanks to the work of hybridizers,
Streptocarpus now come in a range of colours. These include reds, pinks, purples, blues, yellows, whites, and near-blacks. The only colour that is so-far not available is a true orange. Flowers now exist that are multicoloured, striped, spotted, veined, double, larger or smaller, and even fragrant and colour-changing. There are also variegated-leaf varieties, such as
S. 'Canterbury Surprise'. Flower stems may be short or tall; leaves may be big or small; flowers may be full or dainty; and there may be one or many flowers per stem.
AGM cultivars The following hybrid
cultivars have gained the
Royal Horticultural Society's
Award of Garden Merit:- • 'Bethan' (violet-blue, striped) • 'Blue Frills' • 'Burgundy Ice' (burgundy edged white) • 'Carys' (lavender/purple) • 'Charlotte' (pale blue/yellow) • 'Crystal Ice' (white veined with violet-blue) • 'Falling Stars' (pale blue sport of S. johannis, very floriferous) • 'Frosty Diamond' (white, blue, purple) • 'Gloria' (pale pink) • 'Hannah' (light pink/white) • 'Harlequin Blue' (soft blue, yellow, purple line) • 'Harlequin Lace' (pale blue, purple blotches on white) • 'Jennifer' (pale violet-blue with darker veining) • 'Jessica' (mid-pink) • 'Katie' (white with purple blotches) • 'Kim' (deep violet) • 'Laura' (pale pink with maroon veining) • 'Pearl' (white/yellow) • 'Polka-Dot Purple' • 'Rubina Rose' (mid-pink) • 'Sioned' (magenta/pale pink) • 'Snow White' (white, yellow throat) • 'Stella' (pink with deeper veining) • 'Susan' (magenta, yellow throat) • 'Tina' (pink lower lobes deeper pink) • 'White Butterfly'
Genes and inheritance The following is a quick summary of 1950s publications by Lawrence and Sturgess,
Colour genes V = places pigment in the flower stems
F = places pigment in the petal cells V and F are both necessary to give colour, but do not control which colour. When V or F are recessive (vv or ff) the flowers will lack any colour and will be white in appearance.
I = colour intensity. II = intense colour, Ii = medium colour and ii = pale colour. This gene doesn't control "which colour", just how "intense" the final colour will be in appearance. The actual flower colour genes are named
O,
R, and
D. Where the second copy of the gene is given as a "_", the second copy can be either dominant or a recessive. For example, in blue flowers, only one dominant of each the three genes is needed (e.g. the O gene could be either OO or Oo, and it wouldn't matter which).
Blue = O_R_D_
Magenta = ooR_D_
Pink = oorrD_
Mauve = O_R_dd
Rose = ooR_dd
Salmon = oorrdd Other genes affect the
pattern of colour or modify the final colour. Some of these genes are:
B = gives a blotch of colour in the throat of the bloom. The recessive "bb" produces flowers without a blotch. The trait appears to produce a darker or more intense version of the colour of the outer edges of the petals. Thus, you can get dark pink blotches on a lighter pink flower etc.
H = gives colour on the capitate hairs of the pistil. The recessive "hh" gives white or colourless hairs. Genes F, I, B, and H are very closely linked and are usually inherited as a single unit. Therefore, many plants have pigmented flowers with at least medium intensity of color, and blotches in the throat, or have white flowers without blotches.
C = adds a co-pigment to the flower colour. This gene modifies the appearance of the colour, giving a bluish tint to the overall colour. Plants with the recessive "cc" combination have flowers that are "brighter" in appearance. In the Mauve-Rose-Salmon series, the dominant gene produces undesirable murky colours.
L = puts nectar guides in the flower tubes. The recessive "ll" produces flowers without the lines.
Y = puts a yellow central stripe in the flower tube. I suspect that the size of the yellow area changes with "YY" versus "Yy" plants. The recessive "yy" would produce flowers with no yellow in the flower tube. Other genes are mentioned in the original articles, but they appear to involve some rarely seen colour modifications. Genes for plant size, fragrance etc. were not mentioned in these articles. == History of discovery and hybridisation ==