For
the last 70 years, the dominant paradigm in evolutionary science has
been the so-called “new synthesis.” Widely publicized in recent years by
Oxford evolutionary biologist Richard Dawkins, the new synthesis unites
Darwin’s theory of natural selection with Mendelian genetics, which
explains heredity.
The
current crisis in evolutionary science does not imply complete
rejection of this paradigm. Rather, it entails a major, progressive
reorganization of existing knowledge, without undermining the
fundamental tenets of evolutionary theory: organisms alive today
developed from significantly different organisms in the distant past;
dissimilar organisms may share common ancestors; and natural selection
has played a crucial role in this process.
Other
assumptions, however, are under threat. For example, in the traditional
“tree of life” representation of evolution, the branches always move
apart, never merging, implying that species’ ancestry follows a linear
path, and that all evolutionary changes along this path occur within the
lineage being traced. But examination of genomes – particularly
microbes – has shown that genes moving between distantly related
organisms are an important catalyst of evolutionary change.
Moreover,
the new synthesis assumes that the main drivers of evolution are small
mutations generated by chance within a species. But recent evidence
suggests that large changes, caused by the absorption of a chunk of
alien genetic material, may be just as significant. Indeed, the
absorption of entire organisms – such as the two bacteria that formed
the first eukaryotic cell (the more complex cell type found in
multicellular animals) – can generate large and crucial evolutionary
change.
This can create chaotic effects rather than just randomness being behind mutations. For example one mutation might build on another as dependent variables to amplify the effects. For example a mutation might cause R prey to have larger lung, a later mutation to longer legs might then be amplified because the animal already has an extra ability to supply oxygen in this faster running.
This can create chaotic effects rather than just randomness being behind mutations. For example one mutation might build on another as dependent variables to amplify the effects. For example a mutation might cause R prey to have larger lung, a later mutation to longer legs might then be amplified because the animal already has an extra ability to supply oxygen in this faster running.
Further
destabilizing evolutionary theory is the growing realization that many
factors, not just the genome, determine an individual organism’s
development. Ironically, as the discovery of DNA’s structure – initially
lauded as the final act in the triumph of the new synthesis – led to a
better understanding of genomes’ functioning, it ended up weakening
belief in their unique role in directing biological development. Those
who long deplored the omission of development from evolutionary models –
a decades-old critique made under the scientific banner of evolutionary
developmental biology (“evo-devo”) – together with the insistence that
organisms’ development draws on a wide variety of resources, have been
vindicated.
Recent
developments in molecular biology have put the final nail in the coffin
of traditional genetic determinism. For example, epigenetics – the
study of heritable modifications of the genome that do not involve
alterations to the genetic code – is on the rise. And the many kinds of
small RNA molecules are increasingly recognized as forming a regulatory
layer above the genome.
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