It is time the praise was taken back from natural selection
and given to the God of Creation. Taking away the Designers
credit is the crime of the age. One wonders if there is any better
application of this Scripture:
Many scientists who are fine citizens otherwise may without
intention have done just that. Such a course is tragic for them
and for those they teach.
How much more logical for all who investigate and see the
wonders built into all living things that instead we look up in
adoration to Him of whom great throngs in heaven sing, Great
and marvelous are thy deeds, O Lord God, sovereign over all . . .
Who shall not revere thee, Lord, and do homage to thy name?
(Revelation 15:3,4, NEB).
1
David I. Blumenstock, The Ocean of Air (New Brunswick, N.l.: Rutgers
University Press, 1959), p. vii of preface.
2
Francis H. C. Crick, The Language of Life, 1969 Yearbook of Science and
the Future (Britannica), p. 139.
3
George F. Howe and P. William Davis, Natural Selection Reexamined,
Creation Research Society Quarterly, Vol. 8 (June, 1971), p. 43.
4
André de Cayeux, Three Billion Years of Life (New York: Stein and Day,
1969) p. 198. First published in France in 1964.
5
George G. Simpson and William S. Beck, Life: An Introduction to Biology,
Shorter Edition (New York: Harcourt, Brace & World, 1969), p. 143.
6
de Cayeux, Three Billion Years, p. 200.
7
John C. Kendrew, The Thread of Life (Cambridge, Mass.: Harvard University
Press, 1966), pp. 106, 107.
8
More than forty-six trillion times three billion years. This is calculated from
the figures obtained in chapter 2.
9
Simpson and Beck, Life, p. 132.
10
Thomas H. Jukes, Molecules and Evolution (New York: Columbia University
Press, 1966), preface.
Such reverse mutations are common in laboratory work with bacteria. (Roger
Y. Stanier, Michael Doudoroff, and Edward A. Adelberg, The Microbial World,
3rd ed. [Englewood Cliffs, N.J.: Prentice-Hall, Inc., 1970], pp. 471, 472). This
doubtless arises in part from their rapid multiplication rate.
These authors also mention the probability that many good mutations which
occur in experiments with bacteria might nevertheless make the possessors unfit
for survival in the wild: In adapting to existence in laboratory media, organisms
may undergo genetic modifications that would lead to their speedy suppression
in a competitive environment (p. 478).
To understand this principle more clearly, imagine this extreme but comparable
situation: a human being who is by mutation immune to athletes foot (which is
good) because he has no feet (which is bad for the entire organism except in the
most artificial of situations.) An actually existing good/bad mutation makes the
possessor immune to some forms of malaria but also predisposes him to sickle-cell
anemia.
11
Irving Adler, Probability and Statistics for Everyman (New York: John Day
Co., 1963), p. 239.
12
Bolton Davidheiser, Evolution and Christian Faith (Nutley, N.J.: Presbyterian
and Reformed Publishing Co., 1969), p. 212.
13
David Lack, Darwins Finches, Scientific American, Vol.188 (April, 1953),
p.67.
14
Eldon J. Gardner, Principles of Genetics (New York: John Wiley & Sons, Inc.,
1972), p. 358.
Adaptation of animals of the same species to different environments is well
known. Species which in warm climates have short hair may have longer hair
when found in cold climates. Snowshoe rabbits (varying hares) change color from
winter to summer. Any plan by a Creator would doubtless provide a method for
such changes within species. This may perhaps be linked to environmental factors
which trigger the proper genes into action to bring about the needed result by
turning them on. Conceivably, we may speculate, this could also be done through
changes in diet, or even possibly from large alterations in behavior. Such changes
would merely make use of already existing genes that were dormant or turned
off until thus induced into production. Mechanisms for such induction of idle
genes are known at the cellular level
While not necessarily meant to lead to such conclusions, the following statements
of Professor Gardner would give a basis for the preceding hypothesis to
account for adaptability:
We know that environmental factors are interwoven with inheritance mechanisms
at every point in the developmental process (ibid., p. 357). Quantitative
traits, however, are influenced by the environment as well as by inheritance (p.
367). The inheritance of quantitative traits depends upon the cumulative or
additive action of several or many genes, each of which produces a small proportion
of the total effect. This is in marked contrast to the inheritance of qualitative
traits which is an all-or-none phenomenon dependent on one gene or a
few interacting genes. An important consideration in studies of inheritance of
quantitative traits is that environmental factors also have an effect on end products
such as height, weight, or color intensity (p. 119). This might explain variations
in the beaks of Darwins finches.
15
Fred John Meldau, Why We Believe in Creation, Not in Evolution (Denver:
Christian Victory Publishing Co., 1959), p. 19.
16
Björn Sigurbjörnsson, Induced Mutations in Plants, Scientific American
(January, 1971), p. 87.
One may suspect, however, that mutations have by mistake been given the
credit for many changes which were not genetic at all. Authors of a study on
Hawaiian lizard variation in 1973 included this suggestion in their report: Perhaps
environmental heterogeneity may be a very important source of variation in
some morphological characters. (M. E. Soule, et al., Island Lizards: the Genetic-Phenetic Variation Correlation, Nature, Vol. 242 [March 16, 1973], pp. 191-193.)
In line with the hypothesis explained in reference 14 a bit earlier, some of these
outward variations may have resulted from the turning on of existing genes by
environmental stimuli. Some mechanisms for such regulation will be described in
chapter 9.
17
Encyclopaedia Britannica (1967), s.v. mutations.
18
Differential reproduction is currently stressed as the key way natural selection
operates. Organisms who survive to produce greater numbers of viable offspring
will be selected.
19
Richard Goldschmidt, The Material Basis of Evolution (Paterson, N.J.:
Pageant Books, 1960), pp. 390,391. First published 1940.
Goldschmidt made feeble attempts at citing examples. One was the short-legged
dog, the dachshund, which is able to enter badgers dens because of its short legs!
However, the dachshund is bred by genetic engineering and would doubtless not
survive in the wild.
20
L. S. Davitashvili, in Notes and Comments, Evolution, Vol. 23 (September,
1969), p. 514.
21
A. I. Oparin, Genesis and Evolutionary Development of Life (New York:
Academic Press, 1968), p. 130.
22
If all droplets had those catalyst salts, they would be equal, and no selection
could operate. If some, but not all, droplets had such an advantage as better
catalysts, there could be no further progress without an accurate duplicating system.
Each better molecule would be a blind alley. If we consider just the droplets
lucky enough to get these catalyst salts and thereby to monopolize the food
supply, this still provides for no intrinsic improvement, but depends wholly on
external conditions.
23
John Keosian, The Origin of Life (New York: Reinhold Publishing Corp.,
1964), p. 89.
24
Theodosius Dobzhansky, The Biology of Ultimate Concern (New York: New
American Library, 1967), p. 48. (Dobzhansky is an evolutionist, but is quite
definite in his protest against this careless use of the term natural selection to
apply to the era before life existed.)
25
Michael Conrad and H. H. Pattee, Evolution Experiments with an Artificial
Ecosystem, Journal of Theoretical Biology (September, 1970), pp. 405, 406.
These authors did not state their own philosophy regarding evolution in this article.
26
Ibid., p. 406.
27
Charles Darwin, The Origin of Species, Mentor Edition (New York: New
American Library, 1958); all the foregoing quotations are on pp. 96, 97.
28
Ibid., p. 91.