Mutationism is one of several alternatives to evolution by natural selection that have existed both before and after the publication of Charles Darwin's 1859 book, On the Origin of Species. In the theory, mutation was the source of novelty, creating new forms and new species, potentially instantaneously, in sudden jumps. This was envisaged as driving evolution, which was thought to be limited by the supply of mutations.
Before Darwin, biologists commonly believed in saltationism, the possibility of large evolutionary jumps, including immediate speciation. For example, in 1822 Étienne Geoffroy Saint-Hilaire
argued that species could be formed by sudden transformations, or what
would later be called macromutation. Darwin opposed saltation, insisting
on gradualism in evolution as in geology (uniformitarianism). In 1864, Albert von Kölliker revived Geoffroy's theory. In 1901 the geneticist Hugo de Vries gave the name "mutation" to seemingly new forms that suddenly arose in his experiments on the evening primrose Oenothera lamarckiana, and in the first decade of the 20th century, mutationism, or as de Vries named it mutationstheorie, became a rival to Darwinism supported for a while by geneticists including William Bateson, Thomas Hunt Morgan, and Reginald Punnett.
Understanding of mutationism is clouded by the mid-20th century portrayal of the early mutationists by supporters of the modern synthesis
as opponents of Darwinian evolution and rivals of the biometrics school
who argued that selection operated on continuous variation. In this
portrayal, mutationism was defeated by a synthesis of genetics and
natural selection that supposedly started later, around 1918, with work
by the mathematician Ronald Fisher. However, the alignment of Mendelian genetics and natural selection began as early as 1902 with a paper by Udny Yule,
and built up with theoretical and experimental work in Europe and
America. Despite the controversy, the early mutationists had by 1918
already accepted natural selection and explained continuous variation as
the result of multiple genes acting on the same characteristic, such as
height.
Mutationism, along with other alternatives to Darwinism like Lamarckism and orthogenesis, was discarded by most biologists as they came to see that Mendelian genetics and natural selection could readily work together;
mutation took its place as a source of the genetic variation essential
for natural selection to work on. However, mutationism did not entirely
vanish. In 1940, Richard Goldschmidt
again argued for single-step speciation by macromutation, describing
the organisms thus produced as "hopeful monsters", earning widespread
ridicule. In 1987, Masatoshi Nei argued controversially that evolution was often mutation-limited. Modern biologists such as Douglas J. Futuyma conclude that essentially all claims of evolution driven by large mutations can be explained by Darwinian evolution.
Developments leading up to mutationism
Geoffroy's monstrosities, 1822
Prior to Charles Darwin, most naturalists were saltationists, believing that species evolved and that speciation took place in sudden jumps. Jean-Baptiste Lamarck was a gradualist but similar to other scientists of the period had written that saltational evolution was possible.
In 1822, in the second volume of his Philosophie anatomique, Étienne Geoffroy Saint-Hilaire
endorsed a theory of saltational evolution that "monstrosities could
become the founding fathers (or mothers) of new species by instantaneous
transition from one form to the next." Geoffroy wrote that environmental pressures could produce sudden transformations to establish new species instantaneously.
Darwin's anti-saltationist gradualism, 1859
In his 1859 book On the Origin of Species, Charles Darwin denied saltational evolution. He argued that evolutionary transformation always proceeds gradually, never in jumps: "natural selection
acts solely by accumulating slight successive favourable variations, it
can produce no great or sudden modification; it can act only by very
short steps". Darwin continued in this belief throughout his life.
Thomas Henry Huxley warned Darwin that he had taken on "an unnecessary difficulty in adopting Natura non facit saltum ["Nature does not take leaps"] so unreservedly." Huxley feared this assumption could discourage naturalists (catastrophists) who believed that major leaps and cataclysms played a significant role in the history of life.
von Kölliker's heterogenesis, 1864
In 1864 Albert von Kölliker revived Geoffroy's theory that evolution proceeds by large steps, under the name of heterogenesis, but this time assuming the influence of a nonmaterial force to direct the course of evolution.
Galton's "sports", 1892
Darwin's cousin, Francis Galton,
considered Darwin's evidence for evolution, and came to an opposite
conclusion about the type of variation on which natural selection must
act. He carried out his own experiments and published a series of papers
and books setting out his views. Already by 1869 when he published Hereditary Genius, he believed in evolution by saltation. In his 1889 book Natural Inheritance
he argued that natural selection would benefit from accepting that the
steps need not, as Darwin had stated, be minute. In his 1892 book Finger Prints,
he stated directly that "The progress of evolution is not a smooth and
uniform progression, but one that proceeds by jerks, through successive
'sports' (as they are called), some of them implying considerable
organic changes; and each in its turn being favoured by Natural
Selection".
From 1860 to 1880 saltation had been a minority viewpoint, to the
extent that Galton felt his writings were being universally ignored. By
1890 it became a widely held theory, and his views helped to launch a
major controversy.
Bateson's discontinuous variation, 1894
William Bateson's 1894 book Materials for the Study of Variation, Treated with Especial Regard to Discontinuity in the Origin of Species marked the arrival of mutationist thinking, before the rediscovery of Mendel's laws. He examined discontinuous variation (implying a form of saltation) where it occurred naturally, following William Keith Brooks, Galton, Thomas Henry Huxley and St. George Jackson Mivart.
Early 20th century mutationism
De Vries and Mendelian mutationstheorie, 1901
The main principle of the mutation theory is that species and varieties have originated by mutation, but are, at present, not known to have originated in any other way. — Hugo de Vries
Hugo de Vries's careful 1901 studies of wild variants of the evening primrose Oenothera lamarckiana
showed that distinct new forms could arise suddenly in nature,
apparently at random, and could be propagated for many generations
without dissipation or blending. He gave such changes the name "mutation".
By this, de Vries meant that a new form of the plant was created in a
single step (not the same as a mutation in the modern sense); no long
period of natural selection was required for speciation, and nor was reproductive isolation.
In the view of the historian of science Peter J. Bowler, De Vries used the term to mean
large-scale genetic changes capable of producing a new subspecies, or even species, instantaneously.
The historian of science Betty Smocovitis described mutationism as
the case of purported saltatory evolution that Hugo de Vries had mistakenly interpreted for the evening primrose, Oenothera.
De Vries set out his position, known as Mutationstheorie (mutation theory) on the creative nature of mutation in his 1905 book Species and Varieties: their Origin by Mutation.
In the view of the historian of science Edward Larson, de Vries was
the person largely responsible for transforming Victorian era
saltationism into early 20th century mutation theory, "and in doing so
pushed Darwinism near the verge of extinction as a viable scientific
theory".
Johannsen's "pure line" experiments, 1903
In the early 1900s, Darwin's mechanism of natural selection was
understood by believers in continuous variation, principally the biometricians Walter Weldon and Karl Pearson,
to be able to work on a continuously varying characteristic, whereas de
Vries argued that selection on such characteristics would be
ineffective. Wilhelm Johannsen's "pure line" experiments on Phaseolus vulgaris
beans appeared to refute this mechanism. Using the true-breeding
Princess variety of bean, carefully inbred within weight classes,
Johannsen's work appeared to support de Vries. The offspring had a
smooth random distribution. Johanssen believed that his results showed
that continuous variability was not inherited, so evolution must rely on
discontinuous mutations, as de Vries had argued. Johanssen published his work in Danish in a 1903 paper Om arvelighed i samfund og i rene linier (On inheritance in populations and in pure lines), and in his 1905 book Arvelighedslærens Elementer (The Elements of Heredity).
Punnett's mimicry, 1915
In 1915, Reginald Punnett argued in his book Mimicry in Butterflies that the 3 morphs (forms) of the butterfly Papilio polytes, which mimic different host species of butterfly, demonstrated discontinuous evolution in action. The different forms existed in a stable polymorphism controlled by 2 Mendelian factors (genes).
The alleles of these genes were certainly discontinuous, so Punnett
supposed that they must have evolved in discontinuous leaps.
The undermining of mutationism
Yule's analysis of Mendelism and continuous variation, 1902
The undermining of mutationism began almost at once, in 1902, as the statistician Udny Yule
analysed Mendel's theory and showed that given full dominance of one
allele over another, a 3:1 ratio of alleles would be sustained
indefinitely. This meant that the recessive allele could remain in the
population with no need to invoke mutation. He also showed that given
multiple factors, Mendel's theory enabled continuous variation, as
indeed Mendel had suggested, removing the central plank of the
mutationist theory, and criticised Bateson's confrontational approach. However, the "excellent" paper did not prevent the Mendelians and the biometricians from falling out.
Nilsson-Ehle's experiments on Mendelian inheritance and continuous variation, 1908
The Swedish geneticist H. Nilsson-Ehle demonstrated in 1908, in a paper published in German in a Swedish journal, Einige Ergebnisse von Kreuzungen bei Hafer und Weizen (Observations on Crosses in Oats and Wheat),
that continuous variation could readily be produced by multiple
Mendelian genes. He found numerous Mendelian 3:1 ratios, implying a
dominant and a recessive allele, in oats and wheat; a 15:1 ratio for a cross of oat varieties with black and white glumes
respectively, implying two pairs of alleles (two Mendelian factors);
and that crossing a red-grained Swedish velvet wheat with a white one
gave in the third (F3) generation the complex signature of ratios
expected of three factors at once, with 37 grains giving only red
offspring, 8 giving 63:1 in their offspring, 12 giving 15:1, and 6
giving 3:1. There weren't any grains giving all white, but as he had
only expected 1 of those in his sample, 0 was not an unlikely outcome.
Genes could clearly combine in almost infinite combinations: ten of his
factors allowed for almost 60,000 different forms, with no need to
suppose that any new mutations were involved. The results implied that
natural selection would work on Mendelian genes, helping to bring about
the unification of Darwinian evolution and genetics.
Similar work in America by Edward East on maize in 1910 showed the same thing for biologists without access to Nilsson-Ehle's work. On the same theme, the mathematician Ronald Fisher published "The Correlation Between Relatives on the Supposition of Mendelian Inheritance" in 1918,
again showing that continuous variation could readily be produced by
multiple Mendelian genes. It showed, too, that Mendelian inheritance had
no essential link with mutationism: Fisher stressed that small
variations (per gene) would be sufficient for natural selection to drive
evolution.
Castle's selection experiments on hooded rats, 1911
Starting in 1906, William Castle carried out a long study of the effect of selection on coat colour in rats. The piebald or hooded pattern was recessive to the grey wild type.
He crossed hooded rats with the black-backed Irish type, and then
back-crossed the offspring with pure hooded rats. The dark stripe on the
back was bigger. He then tried selecting different groups for bigger or
smaller stripes for 5 generations, and found that it was possible to
change the characteristics way beyond the initial range of variation.
This effectively refuted de Vries's claim that continuous variation
could not be inherited permanently, requiring new mutations. By 1911
Castle noted that the results could be explained by Darwinian selection
on heritable variation of Mendelian genes.
Morgan's small Mendelian genes in Drosophila, 1912
By 1912, after years of work on the genetics of Drosophila fruit flies, Thomas Hunt Morgan
showed that these animals had many small Mendelian factors on which
Darwinian evolution could work as if variation was fully continuous. The
way was open for geneticists to conclude that Mendelism supported
Darwinism.
Muller's balanced lethal explanation of Oenothera "mutations", 1918
De Vries's mutationism was dealt a serious if not fatal blow in 1918 by the American geneticist Hermann Joseph Muller. He compared the behaviour of balanced lethals in Drosophila with De Vries's supposed mutations in Oenothera, showing that they could work the same way. No actual mutations were involved, but infrequent chromosome crossovers accounted for the sudden appearance of traits which had been present in the genes all along.
Fisher's explanation of polymorphism, 1927
In
1927, Fisher explicitly attacked Punnett's 1915 theory of discontinuous
evolution of mimicry. Fisher argued that selection acting on genes
making small modifications to the butterfly's phenotype (its appearance) would allow the multiple forms of a polymorphism to be established.
Later mutationist theories
The
understanding that Mendelian genetics could both preserve discrete
variations indefinitely, and support continuous variation for natural
selection to work on gradually, meant that most biologists from around
1918 onwards accepted natural selection as the driving force of
evolution. Mutationism and other alternatives to evolution by natural selection did not however vanish entirely.
Berg's nomogenesis, 1922
Lev Berg proposed a combination of mutationism and directed (orthogenetic) evolution in his 1922 book Nomogenesis; or, Evolution Determined by Law. He used evidence from paleontology, zoology, and botany
to argue that natural selection had limitations which set a direction
for evolution. He claimed that speciation was caused by "mass
transformation of a great number of individuals" by directed mass
mutations.
Willis's macromutations, 1923
In 1923, the botanist John Christopher Willis proposed that species were formed by large mutations, not gradual evolution by natural selection, and that evolution was driven by orthogenesis, which he called "differentiation", rather than by natural selection.
Goldschmidt's hopeful monsters, 1940
In his 1940 book The Material Basis of Evolution, the German geneticist Richard Goldschmidt
argued for single-step speciation by macromutation, describing the
organisms thus produced as "hopeful monsters". Goldschmidt's thesis was
universally rejected and widely ridiculed by biologists, who favoured
the neo-Darwinian explanations of Fisher, J. B. S. Haldane and Sewall Wright. However, interest in Goldschmidt's ideas has reawakened in the field of evolutionary developmental biology.
Nei's mutation-driven evolution, 1987
Contemporary
biologists accept that mutation and selection both play roles in
evolution; the mainstream view is that while mutation supplies material
for selection in the form of variation, all non-random outcomes are
caused by natural selection. Masatoshi Nei
argues instead that the production of more efficient genotypes by
mutation is fundamental for evolution, and that evolution is often
mutation-limited. Nei's book received thoughtful reviews; while Wright, in the conservative journal Evolution, rejected Nei's thinking as mistaken, Galtier, Weiss, Stoltzfus, and Wagner, although not necessarily agreeing with Nei's position, treated it as a relevant alternative view.
Contemporary approaches
Reviewing the history of macroevolutionary theories, the American evolutionary biologist Douglas J. Futuyma notes that since 1970, two very different alternatives to Darwinian gradualism have been proposed, both by Stephen Jay Gould: mutationism, and punctuated equilibria.
Gould's macromutation theory gave a nod to his predecessor with an
envisaged "Goldschmidt break" between evolution within a species and
speciation. His advocacy of Goldschmidt was attacked with "highly
unflattering comments" by Brian Charlesworth, and Alan Templeton. Futuyma concludes, following other biologists reviewing the field such as K.Sterelny and A. Minelli,
that essentially all the claims of evolution driven by large mutations
could be explained within the Darwinian evolutionary synthesis. James A. Shapiro's
claim that molecular genetics undermines Darwinism has been described
as mutationism and an extreme view by the zoologist Andy Gardner.
Historiography
Biologists
at the start of the 20th century broadly agreed that evolution
occurred, but felt that the mechanisms suggested by Darwin, including
natural selection, would be ineffective. Large mutations looked likely
to drive evolution quickly, and avoided the difficulty which had rightly
worried Darwin, namely that blending inheritance would average out any
small favourable changes.
Further, large saltatory mutation, able to create species in a single
step, offered a ready explanation of why the fossil record should
contain large discontinuities and times of rapid change.
These discoveries were often framed by supporters of the mid-20th century modern synthesis, such as Julian Huxley and Ernst Mayr,
as a controversy between the early geneticists—the
"Mendelians"—including Bateson, Johannsen, de Vries, Morgan, and
Punnett, who advocated Mendelism and mutation, and were understood as
opponents of Darwin's original gradualist view, and the biometricians
such as Pearson and Weldon, who opposed Mendelism and were more faithful
to Darwin. In this version, little progress was made during the eclipse of Darwinism,
and the debate between mutationist geneticists such as de Vries and
biometricians such as Pearson ended with the victory of the modern
synthesis between about 1918 and 1950. According to this account, the new population genetics of the 1940s demonstrated the explanatory power of natural selection, while mutationism, alongside other non-Darwinian approaches such as orthogenesis and structuralism, was essentially abandoned. This view became dominant in the second half of the 20th century, and was accepted by both biologists and historians.
A more recent view, advocated by the historians Arlin Stoltzfus
and Kele Cable, is that Bateson, de Vries, Morgan and Punnett had by
1918 formed a synthesis of Mendelism and mutationism. The understanding
achieved by these geneticists spanned the action of natural selection on
alleles (alternative forms of a gene), the Hardy-Weinberg equilibrium, the evolution of continuously-varying traits (like height), and the probability that a new mutation will become fixed.
In this view, the early geneticists accepted natural selection
alongside mutation, but rejected Darwin's non-Mendelian ideas about
variation and heredity, and the synthesis began soon after 1900.
The traditional claim that Mendelians rejected the idea of continuous
variation outright is simply false; as early as 1902, Bateson and Edith Saunders wrote that "If there were even so few as, say, four or five pairs of possible allelomorphs, the various homo- and hetero-zygous
combinations might, on seriation, give so near an approach to a
continuous curve, that the purity of the elements would be unsuspected".
Historians have interpreted the history of mutationism in different ways.The
classical view is that mutationism, opposed to Darwin's gradualism, was
an obvious error; the decades-long delay in synthesizing genetics and
Darwinism is an "inexplicable embarrassment";
genetics led logically to the modern synthesis and mutationism was one
of several anti-Darwinian "blind alleys" separate from the main line
leading from Darwin to the present.
A revisionist view is that mutationists accepted both mutation and
selection, with broadly the same roles they have today, and early on
accepted and indeed offered a correct explanation for continuous
variation based on multiple genes, paving the way for gradual evolution.
At the time of the Darwin centennial in Cambridge in 1909, mutationism
and Lamarckism were contrasted with natural selection as competing ideas; 50 years later, at the 1959 University of Chicago centennial of the publication of On the Origin of Species, mutationism was no longer seriously considered.