It will be understood that these remarks apply to those cases in which
the production of sports is habitual or frequent, and I imagine in
all such examples it will be found that there are indications of
irregularity in the distribution of the differentiations such as to
justify the view that they are not under that geometrical control which
governs the normal differentiation of the parts. The question next
arises whether these considerations apply also to the production of a
bud-sport as a rare exception, but by the nature of the case it is not
possible to say positively whether the appearance of an exceptional
sport is due to the unsuspected presence of a pre-existing fragment of
material having a special constitution, or to the origin, _de novo_, of
such a material. For instance one of the garden forms of _Pelargonium_
known as _altum_ is liable perhaps once in some hundreds of flowers to
have one or two magenta petals. The normal colour is a brilliant red;
and as we may be fairly sure that this red is recessive to magenta the
interpretation would be quite different according as the appearance of
the magenta is regarded as due to the presence of small areas endowed
with magentaness, or to the spontaneous generation of the factor for
that pigment. Either interpretation is possible on the facts, but the
view that the whole plant has in it scarce mosaic particles of magenta
seems on the whole more consistent with present knowledge.
In _Pelargonium altum_ the enzyme causing the magenta colours must
be distributed in very small areas, but a case in which the magenta
is similarly arranged in a much coarser patchwork may be seen in the
_Pelargonium_ "Don Juan," which often bears whole trusses or branches of
red flowers upon plants having the normal dominant magenta trusses. In
most cases there is little doubt that though the magenta flowered parts
can "sport" to red, the red parts could not produce the magenta flowers.
Public-domain text, read in full here on John Shaqi.
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