Darwin's 'One Long Argument' in the Origin
Lecture notes, ca. 1987.
Parenthetical page references are to On the Origin of Species by
Charles Darwin: A Facsimile of the First Edition, edited by Ernst Mayr.
Harvard University Press, 1964.
Darwin refers to the Origin as "one long argument" (p. 459). What is the
"argument"? We have seen Darwin argue along these lines:
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Individuals within a species vary. (See e.g. p. 45: "no one supposes that all
the individuals are cast in the very same mould. These individual differences
are highly important for us, as they afford the materials for natural selection
to accumulate, in the same manner as man can accumulate in any given direction
individual differences in his domesticated productions.")
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Much individual variation is heritable. (E.g. p. 12, "any variation which is
not inherited is unimportant for us"; p. 13, "perhaps the correct way of
viewing the whole subject, would be, to look at the inheritance of every
character whatever as the rule, and non-inheritance as the exception.")
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Organisms multiply at a rate which exceeds the capacity of their environment
to support them, and so many die. (E.g. pp. 63, "A struggle for existence
inevitably follows from the high rate at which all organic beings tend to
increase.... As more individuals are produced than can possibly survive, there
must in every case be a struggle for existence, either one individual with
another of the same species, or with the individuals of distinct species, or
with the physical conditions of life.")
It follows from (1)-(3) that
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Organisms that are better suited to their environments -- "fitter," though
Darwin eschews this expression -- will survive and reproduce at a higher rate
than those which are less well suited to their environments. (E.g. p. 61,
"Owing to this struggle for life, any variation, however slight and from
whatever cause proceeding, if it be in any degree profitable to an individual
of any species, in its infinitely complex relations to other organic beings and
to external nature, will tend to the preservation of that individual, and will
generally be inherited by its offspring.")
The fact captured by (4) is the fact that Darwin calls "descent with
modification," and it is the key to understanding the origin of species. So
Darwin writes in the Introduction to the Origin:
I am fully convinced that species are not immutable; but that
those belonging to what are called the same genera are lineal descendants of
some other and generally extinct species, in the same manner as the
acknowledged varieties of any one species are the descendants of that species.
(6)
The view is expressed in the concluding sentence as well:
There is grandeur in this view of life, with its several
powers, having been originally breathed into a few forms or into one; and that,
whilst this planet has gone cycling on according to the fixed law of gravity,
from so simple a beginning endless forms most beautiful and most wonderful have
been, and are being, evolved. (490)
In a letter to his friend and critic Charles Lyell, Darwin puts it this way:
Grant a simple archetypal creature, like the mud-fish or
Lepidosiren, with the five senses & some vestige of mind, & I believe Natural
Selection will account for production of every Vertebrate animal. (Darwin to
Lyell, 20 October 1859 [CCD 7: 354])
But the "argument" of the Origin is not simply one in favor of descent with
modification. To establish his own conclusion Darwin must show that his explanation of
the beautiful and wonderful adaptedness of organic beings preferable to its
competitors. The most obvious competing explanation is the hypothesis of
intelligent design; and we know that Darwin was well up on the natural theology of his
time and that he held William Paley's Natural
Theology (1802) in very high regard. We should expect Darwin, then, to
articulate reasons for thinking his own account preferable to Paley's.
This is precisely what Darwin does in the Origin. After making a pretty
straightforward statement of his theory in the first half of the book, Darwin
devotes the second half to showing that his theory offers a better explanation
of the data than does "the theory of creation." Darwin and Paley agree that
certain facts require explanation, e.g. the adaptedness of organic beings to
their surroundings. They disagree over the sort of explanation to be offered.
Paley's explanation invokes the designs of an intelligent
being: Paley's claim is that without intelligence there can be no adaptedness of means to ends, no
purposiveness, no intelligible order in nature -- just as the existence of a
watch on a heath requires the existence of a watchmaker. But the explanation
Darwin suggests in the Origin -- "descent with modification" -- doesn't posit a
watchmaker-like intelligent designer. (It doesn't rule out such a designer, of
course; it simply makes no explanatory use of such a being. In the letter to
Lyell cited above, Darwin writes "I have reflected a good deal on what you say
on necessity of continued intervention of creative power. I cannot see this
necessity; & its admission, I think would make theory of nat. select.
valueless.") But how can Darwin show his explanation to be superior to Paley's?
By beating Paley at his own game. Natural Theology is methodologically quite
sophisticated. Paley begins by adducing a number of very striking facts about
organisms, their parts, and their relations with each other. He suggests that
there must be some explanation of these facts -- there must be an answer to the
question why things are this way. It can't simply be a coincidence, e.g., that
the vertebrate eye is so well adapted to see; the odds against are just too
great. Chance, then, is no explanation. Paley then goes on to eliminate other
alternatives to the intelligent designer hypothesis. The gist of his argument
is simple:
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Certain things are true about organisms, e.g. that they are well suited to
their surroundings, that many of them possess organs well adapted to performing
valuable functions, etc.;
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There must be some explanation of these facts;
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The best explanation is one which invokes the designs of an intelligent being;
Therefore
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We have reason to think such a being exists.
Darwin agrees with (5) and (6), but differs with Paley over (7). In fact, (7),
far from being true, is for Darwin the reverse of the truth. Not only is
Paley's designer hypothesis not the best explanation of the facts cited in (5),
it fails to explain some of the most striking facts about organisms and their
surroundings. It is these facts, and the inability of the designer hypothesis
to account for them, that Darwin seizes on in the second half of the Origin.
Darwin's suggestion is that his own theory of descent with modification
accounts for evident facts about organisms and their surroundings that are
inexplicable on the designer hypothesis.
In the concluding chapter of the Origin, in his "recapitulation" of his
argument, Darwin reviews some of the facts that he believes are anomalous on
"the theory of creation," but explicable on the hypothesis of descent with
modification. (A brief Darwinian "explanation" appears in square brackets, but
obviously all of these are controversial; read the rest of the Origin
for the details.).
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No "mark of demarcation" can be drawn between species (supposedly produced
by special acts of creation) and varieties (allowed to be the result of
secondary laws). [The difference between species and variety is conventional:
species are nothing but "strongly marked and permanent varieties."]
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We usually find many varieties within species in regions where many
species of a genus have been produced. [Speciation -- the formation of new
species within a genus -- is simply the production of varieties within a
species on a larger, longer scale.]
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Species of large genera retain the character of varieties, while species
of small genera don't: (i) they differ from each other less than do species of
smaller genera; (ii) closely allied species of larger genera tend to cluster in
small groups around other species. [Large genera are large in part because
their members vary and diverge from each other to fill available niches.
Liability to vary is itself heritable.]
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Forms of life are arranged in groups subordinate to groups, all in a few
great classes. [The tendency of large groups to increase in size and diverge in
character, together with much extinction, accounts for this.]
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"Natura non facit saltum" -- nature is prodigal in variety, niggard in
innovation. [Natural selection acts by accumulating very slight favorable
variations.]
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We find strange animal-surroundings pairs, e.g. birds of woodpecker-like
form feeding on ground insects; upland geese which rarely swim, yet have webbed
feet; thrushes which dive and feed on sub-aquatic insects. [Natural selection
adapts slowly-varying descendants of each form to any unoccupied or
ill-occupied niche. Perfection isn't necessary, only competitive advantage.]
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We find occasional reversions to long-lost characters, e.g. occasional
appearance of stripes on shoulders/legs of several species of the horse genus.
[These species have descended from a striped ancestor; in general the
characters of distant ancestors occasionally display themselves in living
forms.]
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Specific characters -- which distinguish species within a genus -- are
more variable than generic characters -- which distinguish between genera.
[Species are well-marked varieties; they have already varied since they
branched off from the common ancestor in a certain character, by which they
have come to be specifically distinct from each other. The same character would
be more likely still to be variable than the generic ones, which have been
inherited without change for a very long period.]
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Parts developed in an unusual manner (e.g. trunk, tail, beak) in any one
species of a genus are especially liable to variation. [Since the several
species branched off from the common ancestor, this part has undergone an
unusual amount of variability and modification -- witness its unusual shape,
etc. We should expect this to continue.]
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Allied species in considerably different conditions of life follow nearly
the same instincts. [Instincts change by successive slight profitable
modifications; all species of a genus descended from a common ancestor, and so
inherit much in common.]
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Some instincts are apparently not perfect, and are liable to mistakes
(e.g. the moth and the flame); many instincts cause other animals to suffer.
[See explanations of (f) and (j).]
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Offspring of different species which are crossed (i.e. hybrids) follow the
same complex laws in the degrees and kinds of resemblance to their parents as
do the crossed offspring of acknowledged varieties -- i.e. crosses among
species show the same laws of inheritance as crosses among varieties. [See
explanations of (a) and (b).]
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The fossil remains of each formation are intermediate in character between
fossils in formations above (more recent) and below (older). [They occupy
intermediate positions in chains of descent.]
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All extinct beings belong to the same system as recent beings, and fall
either into the same or into intermediate groups. [See (m).]
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The more ancient a fossil is, the oftener it stands in some degree
intermediate between existing and allied groups. [The descended groups have
diverged in character, so the ancestor will appear intermediate compared to its
later descendants.]
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Recent forms appear "higher" or "more developed" or "better adapted" or
"more specialized" than ancient or extinct forms. [The later, better adapted
forms, conquered the older ones.]
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We find a striking parallelism in (i) the distribution of organic beings
throughout space (e.g. similar niches filled with similar organisms), and in
(ii) the geological succession of organic beings throughout time (e.g. similar
developments at similar periods). [Beings in a particular region are related by
ancestry, and the means of modification have remained the same. Given migration
from one part of the world to another we should expect parallelisms of this
sort.]
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On the same continent, under the most diverse conditions, most of the
inhabitants within each great class are related. [They are lineal descendants
of a common ancestor.]
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Oceanic islands are inhabited by a few species; many of these species are
peculiar to these islands; animals which can't traverse wide spaces of ocean
(frogs, terrestrial mammals) don't inhabit oceanic islands, yet other new and
peculiar species (e.g. bats, birds) are found. [Migration with subsequent
modification; see (q) and (r).]
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Whenever many closely allied species inhabit two areas (e.g. two of the
Galapagos Islands), some identical species common to both still exist; and
whenever many closely allied but distinct species occur, many doubtful
forms/varieties occur as well. [The same parents both once inhabited both
areas; the inhabitants of each area are related to the inhabitants of the
nearest source from which immigrants might have been derived.]
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All past and present organic beings constitute one grand natural system,
with group subordinate to group, and extinct groups often falling between
recent groups. [Specific differences are the result of most recent divergences;
genera next, etc. "The real affinities of all organic beings are due to
inheritance or community of descent" (479).]
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Some characters are more serviceable than others for classification --
e.g. adaptive characters, though important for the organism, are unimportant in
classification; characters derived from rudimentary parts, though of little
importance for the organism, are often very valuable in classification;
embryological characters are most valuable. ["The natural system is a
genealogical arrangement, in which we have to discover the lines of descent by
the most permanent characters, however slight their vital importance might be."
(479)]
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We find homologies -- e.g. the framework of bones is the same in a human's
arm, a bat's wing, a porpoise's fin and a horse's leg. [Each structure
represents the gradual modification of parts/organs which were alike in the
original ancestors of the class.]
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The embryos of humans, birds, reptiles and fish are alike; and each is
unlike its adult form. [Successive variations don't always appear at an early
age; the differences appear at later stages in the development of the embryos
into mature forms. The common ancestral form is more evident in embryo than in
adult.]
These are some of the evident facts which Darwin claims are inexplicable on
the designer hypothesis. His own theory, however, explains them -- they are
just what you would expect if his theory is true. The logic of Darwin's
argument is precisely that of Paley's:
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Certain things are true about organisms, e.g. (A)-(X);
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There must be some explanation of these facts;
But instead of Paley's (7) Darwin suggests
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The hypothesis of descent with modification explains (A)-(X) more
satisfactorily than does the designer hypothesis;
from which it follows that
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The hypothesis of descent with modification is to be preferred to the designer
hypothesis.
This is the conclusion of the "one long argument" presented in The Origin of
Species. As Darwin was to put it in his Autobiography, written late
in his life (1876),
The old argument of design in nature, as given by Paley,
which formerly seemed to me so conclusive, fails, now that the law of natural
selection has been discovered. We can no longer argue that, for instance,
the beautiful hinge of a bivalve shell must have been made by an intelligent
being, like the hinge of a door by man. There seems to be no more design in
the variability of organic beings and in the action of natural selection,
than in the course which the wind blows. (Autobiography, ed. Nora
Barlow [Norton, 1958], 87.)
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