Comparison with 1861 |
|
secondary sexual characters,
than in other parts of their organisation; compare, for instance,
the amount of difference between the
males of gallinaceous birds, in which secondary sexual characters are strongly displayed, with the amount of difference between their females; and the truth of this proposition will be granted. males of gallinaceous birds, in which secondary sexual characters are strongly displayed, with the amount of difference between their females; and the truth of this proposition will be granted. 1859 1860 1861 1866 |
males of gallinaceous birds, in which secondary sexual characters are strongly displayed, with the amount of difference between the females; and the truth of this proposition will be granted. 1869 |
females. 1872 |
The cause of the original variability of secondary sexual
characters is not manifest; but we can see why these characters
should not have been rendered as constant and uniform as other
parts of the organisation; for secondary sexual characters have been
accumulated by sexual selection, which is less rigid in its action than ordinary selection, as it does not entail death, but only gives fewer offspring to the less favoured males. Whatever the cause may be of the variability of secondary sexual characters, as they are highly variable, sexual selection will have had a wide scope for action, and may thus readily
have
suc- ceeded suc- ceeded 1861 | succeeded 1859 1860 1866 1869 1872 |
in giving to the species of the same group a greater amount of difference in their sexual characters,
than in other parts of their structure.
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It is a remarkable fact, that the secondary sexual
differences between the two sexes of the same species are generally displayed in the very same parts of the organisation in which the different
species of the same genus differ from each other. Of this fact I will give
in illustration two instances, the first in illustration two instances, the first 1859 1860 1861 1866 |
two instances in illustration, the first 1869 |
in illus- tration the two first instances 1872 |
which happen to stand on my list; and as the differences in these cases are of a very unusual nature, the relation can hardly be accidental. The same number of joints in the tarsi is a character generally
common to very large groups of beetles, but in the Engidæ, as Westwood has remarked, the number varies greatly; and the number likewise differs in the two sexes of the same species:
again
in fossorial
hymenoptera, the manner
of neuration of
the
|
secondary sexual
characters, characters, 1859 1860 1861 1866 1869 | characters 1872 |
than in other parts of their organisation; compare, for instance, than in other parts of their organisation; compare, for instance, 1859 1860 1861 1866 1869 |
are strongly displayed, with 1872 |
the amount of difference between the
males of gallinaceous birds, in which secondary sexual characters are strongly displayed, with the amount of difference between the females; and the truth of this proposition will be granted. males of gallinaceous birds, in which secondary sexual characters are strongly displayed, with the amount of difference between the females; and the truth of this proposition will be granted. 1869 |
males of gallinaceous birds, in which secondary sexual characters are strongly displayed, with the amount of difference between their females; and the truth of this proposition will be granted. 1859 1860 1861 1866 |
females. 1872 |
The cause of the original variability of
secondary sexual secondary sexual 1859 1860 1861 1866 1869 | these 1872 |
characters is not manifest; but we can see why
these characters these characters 1859 1860 1861 1866 1869 | they 1872 |
should not have been rendered as constant and uniform as
other other 1859 1860 1861 1866 1869 | others, 1872 |
parts of the organisation; for secondary sexual characters have been parts of the organisation; for secondary sexual characters have been 1859 1860 1861 1866 1869 |
for they are 1872 |
accumulated by sexual selection, which is less rigid in its action than ordinary selection, as it does not entail death, but only gives fewer offspring to the less favoured males. Whatever the cause may be of the variability of secondary sexual characters, as they are highly variable, sexual selection will have had a wide scope for action, and may thus
readily readily 1859 1860 1861 1866 1869 | readily 1872 |
have
succeeded succeeded 1859 1860 1866 1869 1872 | suc- ceeded 1861 |
in giving to the species of the same group a greater amount of difference in
their sexual characters, their sexual characters, 1859 1860 1861 1866 1869 |
these 1872 |
than in other
parts of their structure. parts of their structure. 1859 1860 1861 1866 1869 |
respects. 1872 |
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It is a remarkable fact, that the secondary
sexual sexual 1859 1860 1861 1866 1869 | sexual 1872 |
differences between the two sexes of the same species are generally displayed in the very same parts of the organisation in which the
different different 1859 1860 1861 1866 1869 | different 1872 |
species of the same genus differ from each other. Of this fact I will give
two instances in illustration, the first two instances in illustration, the first 1869 |
in illustration two instances, the first 1859 1860 1861 1866 |
in illus- tration the two first instances 1872 |
which happen to stand on my list; and as the differences in these cases are of a very unusual nature, the relation can hardly be accidental. The same number of joints in the tarsi is a character
generally generally 1859 1860 1861 1866 1869 | generally 1872 |
common to very large groups of beetles, but in the Engidæ, as Westwood has remarked, the number varies greatly; and the number likewise differs in the two sexes of the same
species: species: 1859 1860 1861 1866 1869 | species. 1872 |
again again 1859 1860 1861 1866 1869 | Again 1872 |
in
fossorial fossorial 1859 1860 1861 1866 1869 | the fossorial 1872 |
hymenoptera, the
manner manner 1859 1860 1861 1866 1869 | neuration 1872 |
of
neuration of neuration of 1859 1860 1861 1866 1869 | neuration of 1872 |
the
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