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| Developmental changes in reproductive parts of
wild parsnip and optimal defense |
| Optimal defense theory is predicated on two fundamental
assumptions: |
| 1.defenses are beneficial--they enhance fitness
relative to undefended organisms when predators, parasites, or pathogens are present. |
| 2.defenses are costly--they reduce fitness relative to
undefended organisms when predators, parasites, or pathogens are absent. |
If defenses are both costly and beneficial, natural selection
will produce defense systems with favorable (greater than one) benefit-cost ratios.
The allocation to defenses within a plant will depend on whether, and how often, the plant
part is attacked and how valuable the plant part is to fitness
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| Reproduction in wild parsnip proceeds through a series of
stages. First, very small buds are produced. These buds expand first into male
flowers and, subsequently, females flowers. If the ovules are successfully
fertilized, fruits develop, which contain seeds. Parsnips are temporally dioecious,
which means their flowers pass through a male stage prior to becoming female. This
is the standard progression in the primary umbel (the first inflorescence to
flower). In later developing secondary and higher order umbels, a proportion of the
flowers never become female and thus never produce fruit. |
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BUDS
MALE FLOWERS FEMALE FLOWERS |
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As this process proceeds,
more and more biomass is incorporated into the reproductive unit. Concomitantly, the
amount of chemical defense, in the form of furanocoumarins,
increases as well, but at a faster rate. Hendrix (1979) discovered that wild
parsnips can compensate for flowers lost to herbivores by producing more inflorescences
containing a higher percentage of flowers that have both male and female stages. In
view of the plant's ability to compensate for lost flowers, the accelerated
investment in furanocoumarins during development was a mystery. |
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The principal
herbivore of parsnip reproductive parts is the parsnip webworm.
This insect feeds on all stages of reproductive development except late stage fruits. We
reasoned that compensation might involve reallocation of resources that would have gone to
structures, had they not been consumed, to production of new infloresences. We
further reasoned that this ability to reallocate would diminish as more and more resources
were incorporated into the reproductive unit. To test this hypothesis, we removed
the primary umbel reproductive units of different sets of small plants in the field
at different developmental stages--female flowers or green fruits. Other plants were
permitted to complete development of seeds in the primary umbel. Total number of
seeds per plant was not significantly reduced if only female flowers were removed (252
seeds vs 358 seeds), suggesting that the compensation mechanism was successful.
However, when green fruits were removed, significantly fewer seeds were produced (190
compared to 358). Thus, the enhanced defense of fruits may function to ensure
survival of offspring that cannot be replaced. |
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| last
updated 1/11/2000 |
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