It was, therefore, a real advantage to the flowers to narrow their
circle of visitors more and more by varying so that only the useful
visitors could gain access to their nectar, and that the rest should
be excluded. Thus there arose 'bee-flowers,' 'butterfly-flowers,'
'hawk-moth flowers,' and, indeed, in many cases, a species of flower
has become so highly specialized that its fertilization can only
be brought about by a single species of insect. This explains the
remarkable adaptations of the orchids and the enormous length of the
proboscis in certain butterflies. Even our own hawk-moths _Macroglossa
stellatarum_ and _Sphinx convolvuli_ show an astonishing length of
proboscis, which measures 8 cm. in the latter species. In _Macrosilia
cluentius_, in Brazil, the proboscis is 20 cm. in length; and in
Madagascar there grows an orchid with nectaries 30 cm. in length,
filled with nectar to a depth of 2 cm., but the fertilizing hawk-moth
is not yet known.
Thus we may say that the flowers, by varying in one direction or
another, have selected a definite circle of visitors, and, conversely,
that particular insect-groups have selected particular flowers for
themselves, for those transformations of the flowers were always most
advantageous which secured to them the exclusive visits of their best
crossing agents, and these transformations were, on the one hand,
such as kept off unwelcome visitors, and, on the other hand, such as
attracted the most suitable ones.
From the botanical point of view the assumption that flowers and
flower-visiting insects have been adapted to each other by means
of processes of selection has been regarded as untenable, because
every variation in the flower presupposes a corresponding one in the
insect. I should not have mentioned this objection had it not come
from such a famous naturalist as Nägeli, and if it were not both
interesting and useful in our present discussion. Nägeli maintained
that selection could not, for instance, have effected a lengthening
of the corolla-tube of a flower, because the proboscis of the insects
must have lengthened _simultaneously_ with it. If the corolla-tube
had lengthened alone, without the proboscis of the butterfly being
at the same time elongated, the flower would no longer be fertilized
at all, and if the lengthening of the proboscis preceded that of the
corolla-tube it would have no value for the butterfly, and could not
therefore have been the object of a process of selection.
Public-domain text, read in full here on John Shaqi.
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