If garden peas with, let us say, reddish-purple flowers are crossed with
white-flowered ones, the progeny will not be a mixture of these colors
but all reddish-purple. If all danger of subsequent cross-fertilization
is excluded this first generation of reddish-purple progeny will
themselves produce reddish-purple and white progeny in the ratio of
three to one. But the extraordinary part of it is that in the third
generation all the white and about one-third of the reddish-purple
plants will breed true to color. The balance of the reddish-purple
plants, which comprise about two-thirds of the second generation, will,
if their seeds are germinated, produce colored as against white-flowered
progeny in the three-to-one ratio. In other words, these artificial
crosses, made by the plant breeder, and this splitting up of hybrids
which has been many times verified, are seen to be very fertile causes
of the origin of new forms of plant life, if only the factor and
character differences in the ancestry be sufficiently complex. With no
two plants precisely alike, with cross-fertilization so nearly
universal, and with all characters, not a single character or factor
expression, as in control conditions likely to be affected by the cross,
it may be seen how fruitful a source of new forms this natural crossing
may be. It is, in fact, not surprising that plants vary, but that the
force of heredity will hold them into such recognizable categories that
the red maple, or white ash, or blue cohosh are, with thousands of other
species, after all fairly definite designations without which talking
and writing about plants would be all but impossible. Some of our most
beautiful garden plants have arisen either as the result of natural
crossing, or crosses deliberately made by the plant breeder. The scores
of forms of the common garden lilac have mostly come about by such
crosses, although many other garden plants have arisen by still another
kind of variability.
The effects of crossing which have been so briefly noted were not
understood, as indeed the cause of them is still unknown, before 1865,
when Gregor Mendel, an Augustinian monk, published the results of his
work on peas, which furnished the basis for all subsequent work on this
kind of variability. His work was neglected until 1900, when what is now
known as Mendel’s law, involving the Mendelian ratio already noted, was
rediscovered by three independent workers. It is now practically
universally accepted as the way in which natural or induced hybrids
transmit their characters.
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