Encyclopedia of Evolution.pdf - Online Reading Center
Encyclopedia of Evolution.pdf - Online Reading Center
Encyclopedia of Evolution.pdf - Online Reading Center
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missing links<br />
Batesian mimicry. Named after a 19th-century British<br />
naturalist who first observed this phenomenon in the Amazon<br />
rain forest (see Bates, Henry Walter), this form <strong>of</strong> mimicry<br />
occurs when nonpoisonous prey (mimics) evolve a resemblance<br />
to poisonous animals (models). The mimic therefore<br />
benefits from the protection afforded by the poisonous models,<br />
without themselves having to expend resources to make<br />
themselves poisonous. Examples include stingless flies that<br />
resemble bees and wasps, and the viceroy butterfly (Limenitis<br />
archippus) that resembles the poisonous monarch butterfly<br />
(Danaus plexippus). If the mimic becomes too common, relative<br />
to the model, the system becomes unstable, because when<br />
the predators occasionally eat the mimic it will not suffer the<br />
consequences that originally selected for the ability to recognize<br />
the model.<br />
Mimicry provides numerous excellent examples <strong>of</strong> natural<br />
selection. Batesian mimicry formed an important piece <strong>of</strong><br />
evidence that Charles Darwin cited in his original presentation<br />
<strong>of</strong> evolutionary theory (see Darwin, Charles; origin<br />
<strong>of</strong> species [book]).<br />
Further <strong>Reading</strong><br />
Kaiser, Roman. “Plants and fungi use scents to mimic each other.”<br />
Science 311 (2006): 806–807.<br />
Ruxton, Graeme D., Thomas N. Sherratt, and Michael P. Speed.<br />
Avoiding Attack: The <strong>Evolution</strong>ary Ecology <strong>of</strong> Crypsis, Warning<br />
Signals and Mimicry. New York: Oxford University Press, 2005.<br />
missing links “Missing links” refers to fossil evidence <strong>of</strong><br />
evolutionary transitions that has not been found. The term<br />
makes little sense today, as practically all “missing links”<br />
have been found. This is particularly amazing when one considers<br />
the low probability that any individual, or even any<br />
species, might be preserved (see fossils and fossilization).<br />
Fossils have been found that confirm most <strong>of</strong> the transitional<br />
states between major (and minor) groups <strong>of</strong> organisms.<br />
For example:<br />
• The transition <strong>of</strong> reptiles to birds required the evolution<br />
<strong>of</strong> feathers, the loss <strong>of</strong> tail vertebrae, the loss <strong>of</strong> teeth, and<br />
the development <strong>of</strong> the furcula or breastbone, among other<br />
things. A missing link might have feathers but have reptilian<br />
skeletal features such as tail vertebrae and teeth. Numerous<br />
fossils <strong>of</strong> feathered dinosaurs have been found, as well as<br />
primitive birds that had teeth (see birds, evolution <strong>of</strong>).<br />
The most famous <strong>of</strong> these fossils is arcHaeopteryx.<br />
• The transition <strong>of</strong> reptiles to mammals required numerous<br />
changes, some <strong>of</strong> which can be preserved in fossils. One<br />
<strong>of</strong> these is the transition <strong>of</strong> some reptilian jawbones into<br />
mammalian ear bones, and the relocation <strong>of</strong> the jaw joint.<br />
A missing link might have intermediate jawbones and two<br />
jaw joints, one reptilian and one mammalian. A series <strong>of</strong><br />
such fossils, the therapsids or mammal-like reptiles, has<br />
been found that displays these features, including some<br />
with two jaw joints (see mammals, evolution <strong>of</strong>).<br />
• The transition <strong>of</strong> terrestrial mammals to whales required,<br />
among other things, the loss <strong>of</strong> hind legs, the transition <strong>of</strong><br />
front limbs from legs into paddles, and the migration <strong>of</strong> the<br />
nostrils to the top <strong>of</strong> the head. A missing link might have<br />
small limbs and a skull intermediate between that <strong>of</strong> terrestrial<br />
mammals and modern whales. A series <strong>of</strong> such fossils<br />
has been found (see whales, evolution <strong>of</strong>).<br />
It is not always certain that the transitional fossil or<br />
fossils are actually the direct ancestors <strong>of</strong> the modern forms.<br />
Archaeopteryx is a good example. There were other birds<br />
that had more modern characteristics and that lived soon<br />
after Archaeopteryx. Therefore Archaeopteryx itself may<br />
not have been an ancestor <strong>of</strong> modern birds. It was probably<br />
a cousin, not an ancestor. Archaeopteryx and the true ancestor<br />
<strong>of</strong> modern birds descended from a common ancestor,<br />
and Archaeopteryx had evolved less than the ancestor <strong>of</strong><br />
modern birds at the time that Archaeopteryx lived. Archaeopteryx<br />
is very clear confirmation <strong>of</strong> a transitional state<br />
between Mesozoic dinosaurs and modern birds. Feathered<br />
dinosaurs lived at the very time that one would expect them<br />
to have lived, if birds evolved from dinosaurs, but scientists<br />
are not sure which feathered dinosaur might have been the<br />
true ancestor.<br />
In some cases, the evolution <strong>of</strong> a complex adaptation<br />
might appear improbable or even unbelievable. This is one<br />
<strong>of</strong> the major claims <strong>of</strong> intelligent design. In such cases,<br />
the discovery <strong>of</strong> a fossil “missing link,” or the living descendant<br />
<strong>of</strong> a “missing link,” can demonstrate that the complex<br />
adaptation did, in fact, evolve, even if an observer could<br />
not have imagined how. One example <strong>of</strong> many is the complex<br />
set <strong>of</strong> adaptations displayed by desert cacti such as the<br />
saguaro <strong>of</strong> the American southwest. Such cacti can survive<br />
and flourish in desert areas because they carry out photosynthesis<br />
and store water in thick green stems rather than<br />
leaves. In order to do this, cacti underwent several evolutionary<br />
modifications. Their leaves were reduced to small and<br />
temporary structures that did not carry out photosynthesis;<br />
stomata, the pores normally found on leaves, developed<br />
on stems instead; bark development was suppressed on the<br />
stems, allowing them to be s<strong>of</strong>t and green rather than hard<br />
and brown; instead <strong>of</strong> many small branches, they developed<br />
large, thick branches that stored water; and they developed a<br />
modified form <strong>of</strong> photosynthesis known as CAM (see photosynthesis,<br />
evolution <strong>of</strong>). So complex are these adaptations<br />
that some observers are tempted to attribute them<br />
to special creation. But, in fact, there are several species <strong>of</strong><br />
plants <strong>of</strong> the genus Pereskia which are almost perfect intermediates<br />
between desert cacti and their ancestors. They live<br />
in dry mountainous areas <strong>of</strong> Central and South America.<br />
Pereskia plants have leaves, even though they are succulent<br />
leaves; some have stem stomata, some do not; some have<br />
delayed bark formation, some do not. All <strong>of</strong> them are bushes<br />
or trees, rather than having succulent branches. Even their<br />
flowers are intermediate between those <strong>of</strong> desert cacti and<br />
their ancestors. Many have succulent leaves, and some <strong>of</strong><br />
them can use CAM under drought conditions. They closely<br />
resemble the “missing links” that must have existed around<br />
30 million years ago.<br />
Throughout this encyclopedia, transitional forms are discussed.<br />
This next section focuses on “missing links” that seem