Coevolution is the the mutual evolutionary influence between two species (the evolution of two species totally dependent on each other). Each of the species involved exerts selective pressure on the other, so they evolve together. Coevolution is an extreme example of mutualism. Some examples of coevolution include:
Yucca flowers are a certain shape so only that tiny moth can
pollinate them. The moths lay their eggs in the yucca flowers and the
larvae (caterpillars) live in the developing ovary and eat yucca
seeds.
Acacias are small, Central American trees in the Leguminosae. They have
large, hollow thorns. The acacia ants live in the thorns. On the tips
of its leaflets, the plant makes a substance used by the ants as food.
The ants defend the tree from herbivores by attacking/stinging any animal
that even accidentally brushes up against the plant. The ants also prune
off seedlings of any other plants that sprout under “their” tree
Lichens are composed of a mixture of fungi and algae. In each “species”
of lichen, the alga and fungus are so closely intertwined that whole
lichens are classified as species, rather than the component
fungus/alga. The type of fungus and alga are species-specific. The
alga does photosynthesis and produces sugars for fuel for both. The
fungus attaches the whole lichen to its substrate (tree, rock) and holds
in water needed by the alga.
Coevolution is often seen in a number of species of flowering plants that
coevolved with specific pollinators (insects, bats, etc). The pollinator
gets a reward such as nectar for pollinating the plant. Moth-pollinated
plants often have spurs or tubes the exact length of a certain moth’s
“tongue.” For example, Charles Darwin predicted the existance of a moth
in Madagascar based on the size and shape of a flower he saw there. The
moth was actually discovered about 40 years later. The common
snapdragons that many people plant in their gardens are designed for a
bumblebee of just the right weight to trip the opening mechanism.
Some plants (pine, grasses, ragweed) are wind-pollinated. Their
reproductive strategy is to produce lots of pollen in hopes that some
makes it to the female. These plants expend much energy in making
pollen.
Many plants depend on animals to spread their pollen. This is a
mutualistic relationship where the plant and the pollinator benefit each
other. The plant expends less energy on pollen production and instead
produces showy flowers, nectar, and/or odors. Some plants/flowers are
more general, while others are more specific.
The hypothetical evolution of pollination and angiosperms is tied together.
Early gymnosperms and angiosperms were wind-pollinated. Like modern
gymnosperms, the ovule exuded droplets of sap to catch pollen grains.
Insects (beetles) on the plant found this protein/sugar mix and used it
as food. Insects then became dependent on this food source and started
carrying pollen from plant to plant. Beetle-pollination must have been
more efficient than wind for some species, so there was natural selection
for plants that attracted insects.
For pollination to work, to be effective, a relationship must be established between the pollinator and the blossom to be pollinated, involving:
The pollinator should visit this particular blossom regularly. These
visits (whatever the cause) should constitute a regular part of the life
activities of the animal. The visitor must perform or at least try to
perform certain tasks that are tied in with the structure and function
of the blossom. Insects that happen to visit a couple flowers and
transfer pollen don’t count as pollinators of that species unless they
regularly visit that species of plant for some specific reason.
The plant must supply:
Adaptations of flowers depend on the type of pollinator on which they depend.
Bees don’t see red, but do see yellow, blue, and UV. Thus,
bee-pollinated flowers are mostly yellow or blue with UV nectar guides
(landing patterns) to guide the bee. They usually have a delicate,
sweet scent, and a small, narrow floral tube to fit the tongue-length
of that species of bee. The flowers are sturdy and irregularly-shaped
with a specifically-designed landing platform. For example,
snapdragons will only open for a bee of the right weight.
Butterflies are diurnal and have good vision (can see red) but a
weak sense of smell. They are perching feeders. Butterfly-pollinated
flowers are brightly-colored but odorless. Often, these flowers occur in
clusters (Compositae, milkweed) and/or are designed with a “landing
platform.” Butterflies walk around on flower clusters probing the
blossoms with their tongues. Each flower has a tube of suitable length
for the butterfly’s tongue.
Moths are nocturnal, have a good sense of smell, and are
hover-feeders. These flowers are white or pale colors so they are
visible at night, and may only be open at night. Typically, these
flowers have a strong, sweet scent (again, maybe only at night) and deep
tubes to match the length of the appropriate moth’s tongue. The petals
are flat or bent back (recurved) so the moth can get in.
Birds, especially hummingbirds have good eyes which expecially
can see red but poor senses of smell. These flowers are brightly-colored,
especially red, but have no smell, and have recurved petals so they are
out of the way. Hummingbirds are hover-feeders, and these flowers (for
example, columbine or fuchsia) are designed to dust the bird’s head
(and back) with pollen.
Flies are attracted to rotting flesh. These flowers may be
nondescript or may be brownish-red with a bad, rotten smell as their
main attractant. Some flowers, near the ground, are pollinated by
ants or ground beetles.
On the other hand, some plants have not specifically coevolved with a
certain pollinator. Canada thistle flowers are visited by a wide variety
of bees, beetles, and butterflies.
Similarly, goldenrod flowers attract a variety of beetles, wasps, and
other small insects which, in turn, may be food for waiting spiders.