Within this framework there are other, presumably subordinate, factors
that influence the values of breeding indices, as follows:
1. Migratory habit. Any migrant tends to arrive on breeding grounds
relatively late, hence migrants ordinarily have higher index values than
do residents.
2. Colonial breeding. The strong synchrony of colonially-breeding
species tends to move the modal egg-date toward the time of inception of
breeding; as a result colonially-breeding species probably have lower
index values than they would have if not colonial.
3. Single-broodedness. Species having only one brood per season tend to
have shorter seasons than double-brooded species, and their index values
tend to be lower than those of double-brooded species.
Migratory habit unquestionably has considerable influence on index
values in some species. It is not, however, as important as other
matters, such as the condition of the food substratum or sensitivity of
the pituitary-gonadal mechanism, in determining timing and mode of
breeding activity. The schedule of the Purple Martin is the extreme
example showing that time of spring arrival on breeding grounds is not
necessarily related to time of inception of breeding. It should be
emphasized that the factors leading to northward migratory movement may
be involved in timing of the annual gonadal and reproductive cycle.
Figure 2 presents a graphic summary of values of breeding indices for
many groups of Kansan birds. The values for species of a given family
have been linked by a horizontal line. The length of this line is
proportional to the degree to which the index values for the species
concerned resemble one another. Note that the plottings for the Picidae,
Corvidae, Turdidae, Tyrannidae, and Icteridae each contain one point
that is well-removed from a cluster of points. This can be interpreted
as a measure of the frequency of adaptive plasticity versus adaptive
conservatism; five of the 24 plottings show a plastic character, 19 a
conservative. There are 26 plottings that show temporal consistency, all
of which may be taken as evidence of adaptive (or relictual)
conservatism of the species in question.
[Illustration: FIG. 2.--Breeding indices for Kansan birds.
Vertical hash-marks indicate the value of breeding index for a
given species; horizontal lines show the range of values of
breeding index for families and orders.]
_Conclusion_
Such patterns of breeding chronology support the idea that seasonal
response to the necessities of breeding is conservative more often than
plastic. Most students of breeding schedules believe that since these
are highly adaptive, they must also be capable of flexibility to meet
variable environments within the range of the species. Such thinking
receives support when different geographic localities are considered for
one species (Johnston, 1954), or when specific features of a special
environment are considered (see Miller, 1960; Johnston, 1956).
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