This book is an original, valuable contribution to creationist thought, especially
in the area of biology, although the author touches on other fields.
The theme permeating the book is that a supernatural creator has placed a pattern
in living things (and their fossils) which defies a naturalistic explanation and
points the observers to the one intelligent designer. This is The Biotic Message:
the unity in biology tells us that there is but one Creator, and the pattern of
diversity defies any consistent naturalistic explanation.
‘Similarity makes life look like the work of one designer, while diversity
makes life difficult to explain by naturalistic processes’ (p. 37).
ReMine highlights area after area of evolutionary thought where hypotheses are constructed
in such a way as to be untestable (that is, not scientific), or illogical. In the
preface, ReMine says that he pursued the hobby of magic (illusion) for many years
and that this prepared him well for the job of exposing evolutionary illusions.
He does this masterfully as illusion after evolutionary illusion is exposed. A simple
example of evolutionary illusion, based on the misuse of terminology, is the statement
by evolutionists that ‘fish gave rise to amphibians and amphibians gave rise
to reptiles’. Such a statement gives the illusion of phylogeny—that
there is here an evolutionary sequence—and yet no sequence has been identified.
Which species of fish gave rise to which species of amphibian? And which species
of amphibian gave rise to which species of reptile? And which fossils show the transitions?
ReMine begins with more general arguments against naturalism in science. He shows
how scientists can be inconsistently selective in what they allow as ‘science’.
Naturalists say that science can say nothing about an intelligent cause for the
universe/life, etc. However, these same naturalists will acknowledge that science
can identify human artefacts in archaeology, because they have the characteristics
of an intelligent, as distinct from natural, cause. Science can also detect fraud
(for example, Piltdown Man), which has an intelligent unseen cause, and can recognise
other patterns in nature that could not have a natural cause—that is, they
must come from an intelligent (and unseen) cause—the SETI programme is tacit
acknowledgement of this.
Testability/falsifiability is widely recognised as the major criterion for science.
A theory must also have explanatory value. Evolutionists will often charge that
creation theory is unfalsifiable but then argue that it is falsified. They will
also formulate evolutionary propositions in such a way that they are a tautology
(a truism), or metaphysical, or lame. ReMine illustrates this with the various formulations
of the anthropic principle:
Tautology: the universe has the (observable) properties for life because we live
(and observe). ReMine says (p. 174) that ‘a tautology is a definition masquerading
as an explanation’.
Metaphysical: there are an infinite number of universes unlike our own. We are in
one of the ones suitable for life (this is untestable—how could you test whether
there are other ‘universes’?)
Lame: the constants take on the values restricted by the requirement that there
are sites where carbon-based life can evolve and by the requirement that the universe
be old enough for it to have already done so (after Barrow and Tipler1). This statement explains nothing and is therefore
ReMine points out that science is limited—using Gödel’s Incompleteness
Theorem, which basically says that no body of mathematical knowledge can be self-contained
or self-authenticating. In other words, there are unprovable true theorems and man
can never have all the answers.
So knowledge cannot be self-referencing. By extension, this means that science cannot
fully understand nature in terms of nature. If this is attempted, we can expect
contradictions and paradoxes. This, I believe, is another way of saying Romans 1:18–23.
ReMine also argues from the ‘Big Bang’ and the laws of thermodynamics
for an origin to the universe. The universe is not eternal; it had a beginning.
Anything which has a beginning has a cause and therefore it demands a creator. Here
I would prefer that he stick to the laws of thermodynamics alone to demonstrate
this. Accepting the Big Bang model gives too much ground to the naturalists and
implies that the billions of years are real.
ReMine’s treatment of the origin of life is good. I particularly liked the
way he dealt with some of the bluffs of evolutionists who try to dilute the improbability
argument with irrelevant analogies. For example, the exact arrangement of the cards
in a deck just after it is shuffled is highly improbable, but nevertheless an improbable
arrangement happens every time. This confuses the point entirely. The question is
not ‘what is the probability that life arose?’ but ‘what is the
probability that life could arise naturalistically, without the involvement of an
intelligent creator?’. Any arrangement of cards is as ‘good’ as
any other and there will be an arrangement of cards. However, with
the DNA code, a particular arrangement is required. If we got an arrangement of
cards with an orderly pattern (Ace, King, Queen, Jack, etc.) we would conclude that
someone had ‘stacked the deck’; that is, an intelligence was responsible
because such an arrangement is so unlikely from random shuffling (the probability
of such an arrangement from random shuffling is less than 1 in 1067).
Many a card cheat has paid the price of this powerful evidence of intelligent input!
Evolutionists want us to believe that something far less likely than the orderly
arrangement of cards happened without intelligent input—and they use irrelevant
analogies to try to avoid the argument.
ReMine also points out that evolutionists claim that the biologic universals such
as RNA, DNA, ATP, etc. are evidence for the common ancestry of all things. However,
evolution never predicted that life would arise only once and only
based on the DNA-protein code we have. Furthermore, they have rejected each of the
biologic universals in attempts to build origin-of-life scenarios (for example,
the ‘RNA-first’ idea), showing that the universality of the DNA-protein
system is definitely not a prediction of evolution. However, it is a prediction
of ‘message theory’ that there would be a unifying principle underlying
all living things which shows that there was only one message sender (creator).
Furthermore, the DNA code defies a naturalistic explanation; no wonder that many
evolutionists have tried to exclude the origin of life from debates with creationists.
ReMine labours the tautological nature of ‘survival of the fittest’,
or natural selection, as the evolutionary explanation of adaptation and design.
I found this a bit tedious. He shows that efforts to define it in a testable/falsifiable
way result in either metaphysical or lame formulations which may sound testable/falsifiable
but in practice are not, or have no explanatory value. ReMine describes this exercise
as ‘the intellectual equivalent of a carnival three-shell game’ (p.
The formulation of special definitions results in many disjointed, conflicting theories
parading as a unified theory. For example, in one context evolutionists will argue
that female mosquitos are bigger than the males because the female is responsible
for egg-laying and the male only has to contribute a little sperm, so bigger females
make for greater reproductive success. But in another context, evolutionists will
argue that male lions are bigger than the females because the bigger males have
greater dominance over other males in the mating game and therefore they will mate
with more females and pass on their genes. Both stories sound plausible in isolation,
but they ‘explain’ contradictory states of affairs and so have no value
in prediction. Such special definitions, or story-telling, do not add up to make
a valid scientific theory. Special definitions, which are measurable, testable and
explanatory, are only true for special cases and do not provide any unifying theory
to explain adaptation in general.
The arguments woven into the discussion of natural selection are fascinating: the
way in which evolutionists choose from a smorgasbord of competing and conflicting
theories in attempts to explain adaptation.
The chapter on Darwinian Scenarios (6) was especially entertaining. Here ReMine
shows how Darwinism is story-telling. Darwinists will be very inventive at story-telling
when it suits them, but also seem to lack imagination when it suits them. Riddiford
and Penny’s challenge2 for creationists
to find a non-adaptive structure in nature to disprove Darwinism—such as a
‘bird’s nest’ structure built into an elephant’s back—is
a case in question. ReMine shows how their challenge is quite hollow. An adept Darwinist
would have no trouble thinking of reasons for this structure being adaptive (that
is, it benefits the elephant and therefore would be selected by natural selection).
And ReMine provides some amusing suggestions in the style of Darwinists. At every
turn, ReMine shows how evolutionary theory predicts nothing, but is used after the
fact to ‘explain’ adaptations with ‘just-so’ stories and
‘most any circumstance can be accommodated by evolutionary scenarios’
The various attempts to explain the advent of sexual reproduction illustrate evolutionary
story-telling beautifully (pp. 196–206). In the Darwinian struggle to pass
on genes to the next generation, asexual reproduction is twice as efficient as sexual
because with the latter your genes are diluted by your mate’s. Adding other
disadvantages (such as sharing food resources with ‘useless males’)
results in more than 50 % cost of sexual reproduction. Why then did sex arise? The
conflicting story-telling makes for interesting reading. ReMine argues that sex
has two features necessary for the biotic message: substantial presence throughout
various life-forms (the unifying effect: one designer); and it resists a naturalistic
Various Darwinists have proposed tests which could refute evolution. For example,
Darwin said that an example of truly altruistic behaviour would disprove the theory.
However, dandelions produce nectar, which benefits insects, but have no need of
the visits from the insects because dandelions reproduce asexually. But then the
story-telling comes into play to rescue the theory: dandelions originally reproduced
sexually so produced nectar for their own benefit but have since lost the need for
it!Another example: Michael Ruse argues that organisms could not evolve a second
time, and if they did, it would refute Darwinism (p. 151). But some foraminifera
have re-appeared in the fossil record after disappearing, and knowing this, Schafersman
says that ‘evolution does not assume or require nonrepeatability’.
Evolutionary theory is so plastic it can conform to any data.
Natural selection is highly efficient or inefficient as the case demands: it could
not get rid of the wasteful production of nectar by dandelions, but it supposedly
got rid of the keen sense of smell of apes as they evolved into humans (not to mention
the ability to synthesise ascorbic acid).
Bacteria, fungi and protozoa have cellulase enzyme which allows them to digest cellulose,
one of the most abundant compounds in nature. Multicellular organisms lack the ability
to digest cellulose. If micro-organisms gave rise to multicellular organisms, why
did they lose such a useful ability? Or, if ‘convergences’ are so easy
for evolution to produce (for example, the thylacine, or marsupial wolf, and the
placental wolf, marsupial mole and placental mole, flying phalanger and flying squirrel,
etc.), why has not the ability to digest cellulose evolved in multicellular organisms?
ReMine argues that this pattern is exactly what one would expect from a biotic message
sender: it makes sense ecologically, because plants need to be protected from over-grazing
by multicellular animals to preserve ecological balance in the system of life. But
why should evolution stop multicellular organisms from developing a cellulase?
Convergences are consistent with ‘message theory’, says ReMine, because
they unify life, they thwart phylogeny and they resist naturalistic explanation
Population Genetics, Haldane’s Dilemma and the Neutral
Theory of Evolution
These chapters (7–9) were probably the highlight of the book for me. ReMine
does a masterful job of exposing the fallacy that population genetics supports evolutionary
ideas. It is quite the contrary. Population genetics does not explain adaptation;
it describes changes in gene frequencies, given a certain ‘fitness’,
and fitness cannot be measured before the event. If we have certain stable allele
frequencies in a population, we can calculate from population genetics the ‘relative
fitness’ of each allele, but this is then a tautology: fitness is defined
in terms of survival. Survival does not explain fitness/adaptation.
The theorems of population genetics are mathematical constructs that say nothing
about evolution as such. However, population genetics is quite useful for testing
various evolutionary (and creationist) scenarios.
Population genetics is hampered by the assumptions of the ‘bean bag model’.
In this simplistic model each gene acts independently of other genes. In the real
world genes often affect more than one trait (pleiotropy), or more than one gene
affects a given trait (polygeny).
ReMine shows how evolutionists, including some big name ones, have misapplied Fisher’s
‘Fundamental Theorem of Natural Selection’, which actually says nothing
about natural selection. It is a theorem about average population growth rates,
given the growth rates of distinct sub-populations. It does not predict that evolutionary
progress is inevitable, as many evolutionists have claimed.
ReMine deals with Haldane’s Dilemma in a thorough and helpful manner. Haldane
effectively showed that long-generation organisms have not had enough time to evolve,
because of the cost of substitution (the fixing of a new gene in a population requires
the death of those individuals which do not have it), even given assumptions favourable
for evolution (for example, no pleiotropy or polygeny and only minimal consideration
of recessive alleles). ReMine deals with various attempts to deal with the problem—such
as Richard Dawkins’ naïve computer ‘simulation’ of mutation
and natural selection where he uses grossly unrealistic assumptions (such as perfect
selection, a high rate of beneficial mutation, high reproductive rate, a pre-determined
goal, etc.) to produce the fastest possible ‘evolution’. This provides
the illusion that evolution is simple, virtually inevitable, and fast (p. 236).
ReMine also discusses Kimura’s neutral evolution theory, which was basically
an attempt to grapple with Haldane’s Dilemma. Neutral evolution was supposed
to make evolution go faster. However, a high rate of neutral evolution means that
there will be a high rate of expressed neutral mutations, 90 %
of which will be definitely harmful (according to Kimura’s
estimate), and this results in error catastrophe.
This is the incredible rationale behind the ‘more than 99 % inert junk’
claim regarding mammalian DNA. This ‘prediction’ of evolutionary theory
has been falsified by molecular biologists as they have been unravelling the human
DNA code, for example. Even as long ago as 1989, Maynard Smith acknowledged that
9–27 % of the human genome codes for protein (p. 250). This puts all evolutionary
scenarios right out of court.
Using the neutralist approach, ReMine shows that, in 10 million years, a human-like
species could substitute no more than 25,000 expressed neutral mutations and this
is merely 0.0007 % of the genome—nowhere near enough to account for human
evolution. This, ReMine says, is the trade secret of evolutionary geneticists. Evolutionary
genetics textbooks avoid mentioning the problem.
The scientific endeavour requires reductionism, which entails the attempt to break
complex systems down into segments which are amenable to experimentation. ReMine
discusses the ideas of sociobiologists who reduce human emotions and thoughts to
the mere consequences of the selfish gene (after Dawkins) through case-by-case story-telling.
Evolutionary critics such as Gould and Kitcher deride the sociobiologists, but ReMine
shows how their arguments against sociobiology are the same arguments creationists
use against evolutionary biology: story-telling is not science.
Many leading evolutionists disparage ‘reductionism’. ReMine shows that
they are really trying to avoid testability. ReMine ‘translates’ a convoluted
statement by Depew and Weber as follows:
‘The desirability of refuting modern creationism suggests the use of reductionistic
ideals. These ideals have been powerful tools for this in the past, and they still
are. But this should not be taken too seriously because evolutionary biology is
definitely non-reductionistic’ (p. 167).
Hierarchy theory (chapter 15) is another example of evolutionists’ anti-reductionism.
ReMine explains the different methods of classification and the attempts of evolutionists
to conscript classification as evidence for common descent. Evolutionists do this
by presenting the tree structures of cladograms and phenograms, which show the nested
pattern of organisms derived from systematics, as evolutionary trees. They present
cladograms as lineages.
However, cladograms do not identify ancestors and descendants. Actual ancestors
and descendants are not identified—and the fossils do not reveal them, as
ReMine shows through a multitude of quotes from evolutionists who admit the absence
of transitional forms.
ReMine shows how terminology, such as primitive/ancestral and intermediate form/transitional
form, are confused and used to give the impression or illusion of evolution. An
example that comes to my mind is Archaeopteryx. Evolutionists will say
that this is an intermediate between reptiles and birds, giving the impression to
non-specialists that Archaeopteryx forms part of a lineage joining a reptile
with the ancestor of the birds. However, it is not transitional—it
does not form part of any sequence (phylogeny) connecting reptiles and birds. Furthermore,
it is a curious mosaic; none of its traits are transitional. For example, the feathers
are fully developed, similar to extant birds; they are not part scale, part feather.
Its brain case is fully avian, and so on. It has teeth—supposedly a reptilian
feature—but they are like those of some other fossil birds, not reptilian
Another misused term is ‘microevolution’, used to describe the observable
variations seen within basic types of organisms (for example, the famed industrial
melanism of the peppered moth, variation in finch beaks in the Galápagos,
antibiotic resistance, etc.). ReMine rightly argues that creationists should not
use the term ‘microevolution’ as this plays into the hands of the illusion
encouraged by evolutionists: that given enough time, microevolution adds up to macroevolution.
The sort of observable variation evolutionists like to dub as ‘microevolution’
is due to re-arrangement of existing alleles, or degenerative changes, whereas evolution
(‘macroevolution’) requires the formation of new, complex, information-laden
genes to produce feathers on reptiles, for example.
The idea of punctuated equilibrium is discussed. ReMine says that ‘punctuationists
say they read their theory from the fossil record’ (p. 333). Actually,
Gould and Eldredge originally claimed that their theory was derived from the theory
of allopatric (geographic) speciation and concepts of group selection, so that they
then ‘predicted’ the discontinuous fossil record.3 Then they claimed the fossil record validated their
‘predictions’ and therefore their theory. However, I think ReMine is
correct: punctuated equilibrium is basically an attempt to down-play the lack of
evidence in the fossils for phylogeny. It derives from a more ‘literal’
reading of the fossil record. Gould’s insistence on ‘bushiness’
rather than trees also serves to down-play the need for lineages to validate evolution.
So is punctuated equilibrium testable? Gould says that a series of fossils showing
gradual development of an adaptation would refute punctuated equilibrium. ReMine
points out the ‘no lose’ situation that Gould and company have created
here: if the fossils show systematic gaps, then the punctuated equilibrium model
of evolution is ‘proven’, but if the fossils show gradualism, then the
standard neo-Darwinian model of evolution is proven. In other words, evolution itself
is no longer falsifiable! Punctuated equilibrium and neo-Darwinism are both now
part of the evolutionists’ grab-bag of conflicting theories as Gould and Eldredge
now view punctuated equilibrium as an addition to evolutionary theory rather than
Evolution does not predict a single unified pattern in organisms. ReMine points
out that the discovery of an organism having no similarity to any known life would
not falsify evolution, because evolution does not predict its absence. Evolutionary
theory would be immediately adjusted to allow for two systems of life.
Nor does the theory predict the nested pattern evident in classification. If evolved
traits were lost and replaced at a high rate, then a nested pattern would not result.
Descendants could bear little resemblance to their ancestors with no pattern of
nested similarities linking them. As ReMine says:
‘Evolutionary theory predicts nothing, not even a nested hierarchy. Rather,
the theory adapts to data like a fog adapts to landscape’ (p. 350).
He has some interesting perspectives on convergences. Convergences are strikingly
similar, but not identical. If they were identical, the observer could conclude
that transposition occurred (that is, the traits were transferred between basically
different kinds of organisms—for example, by viral action). However, they
are sufficiently similar to demand incredible rationalisations from the evolutionist.
Convergences unify diverse organisms in a way which cannot be explained by common
descent or by transposition. Again we see the unifying pattern with a non-naturalistic
The nested pattern of organisms makes the biotic message resistant to noise due
to such things as extinction or absence of organisms for observation in a given
location, because the pattern does not depend on any particular organism. This makes
the biotic message robust.
Again, the patterns seen in embryology defy naturalistic explanations but present
a unifying message. Evolutionists point to similarities at the pharyngula stage
of vertebrate embryos as evidence of common ancestry. However, at earlier stages
they look quite different, which undermines the argument that similar appearance
at the later phase is due to common ancestry. Furthermore, there are examples of
similar organs which develop from different embryonic tissue—for example,
the octopus eye and the vertebrate eye. And there are different modes of development.
The amniote foot develops by dissolution of intercalary tissue from a plate-like
structure, whereas the very similar amphibian foot develops by radial growth from
buds. Here again the unifying pattern which thwarts naturalism and polytheism.
There is a helpful chapter on vestigial organs.
ReMine presents some interesting insights into molecular evolutionary studies. He
shows that the nested pattern of similarities revealed by molecular methods which
is erroneously interpreted by evolutionists as ‘phylogeny’, effectively
thwarts transposition. He shows that evolutionists would embrace transposition,
if they could, because it would help explain the lack of phylogeny and the large
morphological gaps in the record of life. For example, Syvanen said:
‘The cross-species gene transfer model could help explain many observations
which have puzzled evolutionists, such as rapid bursts of evolution and the widespread
occurrence of parallelism in the fossil record’ (p. 403).
Again, evolutionists are not committed to common ancestry, just to naturalism. The
absence of transposition in multicellular organisms is powerful evidence against
evolution and for the biotic message.
As well as the lack of clear lineages in the fossil record mentioned earlier, ReMine
looks at the devices used by evolutionists to deal with the fossils. A major illusion
of fossil sequence was created by evolutionists labelling fossil species as ancestors
and descendants largely on the basis of their relative position in the strata. Fossil
sequence was used to identify ancestors and then the perfect agreement between the
fossil sequence and ancestors was claimed as evidence for evolution.
ReMine deals with five devices evolutionists use to cope with out-of-sequence fossils
(that is, not in the correct strata to be transitional between others in a lineage).
The two most powerful of these are:–
(1)The two fossils do not have an ancestor-descendant relationship; they belong
to sister groups. This is the approach taken now with the horse evolution story.
We now have evolutionary bushes where lineage cannot be clearly seen. Anything can
appear anywhere with a bush. As ReMine points out, with this scenario, the only
way an out-of-sequence fossil could be demonstrated is by identifying a clear-cut
evolutionary lineage based on morphology and then show that the organisms in the
phylogeny are in the wrong stratigraphic sequence. Because it is not possible
to construct any clear-cut phylogeny, evolution is insulated against out-of-sequence
fossils. As ReMine says:
‘The evolutionist need only claim that the organisms in question do not have
an ancestor-descendant relationship… . And who could argue with that?’
(2)The incompleteness of the fossil record. The earliest occurrence of the truly
earliest species has not been found.
Fossils can be in sequence only if they form a lineage and also appear in the proper
chronological succession in the rock strata. Some evolutionists admit that these
are not found.
ReMine has a helpful chapter where he summarises his case. He firstly discusses
the evolutionists’ criticisms of the ‘two-model approach’ (that
is, there are only two alternatives, and evidence against evolution is evidence
for creation). He shows how evolutionists use the two-model approach themselves.
It can be traced right back to Darwin. Vestigial organs, embryonic recapitulation,
‘imperfections’, biologic universals, life’s nested hierarchy,
etc., have been used ‘against God’. Evolution did not predict any of
these things, but it is so plastic that it could be moulded to fit and provide an
‘explanation’. Stephen Gould used the ‘God would not create the
panda’s thumb’ argument in his well-known book.4
And he co-authored an introductory biology text5
that used this approach.
Evolutionists arrived at another dualism via the two-model approach. They reasoned
that they had proved that ’God did not do it’, so evolution must
have. So evolution is a fact. Then they debate (amongst themselves) about
how it occurred. ReMine calls this the whether/how dualism. Of course, if a theory
says nothing about ’how’ it is not a scientific theory because it explains
Natural selection fails to explain the adaptations of life. The genetic model in
all evolutionary genetics textbooks shows that a human-like population could substitute
no more than 1,667 selectively beneficial nucleotides in ten million years (or possibly
25,000 neutral nucleotides). This is nowhere near enough to account for human evolution,
but the implications are not spelled out, with students left with the impression
that evolution is almost inevitable, easy and rapid.
ReMine summarises the illusions created by evolutionists to encourage acceptance
of naturalism: misuse of terminology (such as intermediate/transitional fossils),
reversals of logic (for example, prove neo-Darwinism to disprove punctuationalism—a
no-lose scenario for evolution), failure to clearly refute discredited ideas (such
as embryonic recapitulation, vestigial organs, biogeography arguments), mis-applying
concepts (such as the nested patterns from classification, portraying them as phylogenies),
the formulation of ideas to make them sound scientific, but are untestable (such
as hierarchy theory and ‘bushiness’ which circumvent the need for phylogeny),
portraying ‘postdictions’ as predictions of evolutionary theory when
evolution is so plastic it could accommodate almost anything.
ReMine summarises the case against evolution, and the case for creation, in that
evolution did not predict the patterns of similarity and diversity in organisms,
whereas ‘message theory’ does. But in the end,
‘when pressed, however, we can say that evolutionary theory—as practised
by its proponents—is unfalsifiable, since that is its essential character’
‘In short, their program is not science. From beginning to end, their program
is driven by an unrelenting commitment to naturalism, at the expense of science’
ReMine claims that evolution is not science, being driven by naturalism, but creation
(or message theory) is science because it makes testable predictions. I think that
ReMine is going a bit far here. I don’t think one can separate the two philosophically
in that way. ReMine’s ’predictions’ from message theory are really
postdictions like those of evolutionists. He has looked at the data and asked, ’how
does this make sense, considering that it was created for the purpose of revealing
the creator?’. Certainly the observations make much more sense from a creationist
point of view, and ReMine has ably shown that evolutionary thought is a mess of
contradictory, ad hoc story-telling, but both deal with past events, which
are not amenable to experimental verification in the present, and both are ultimately
driven by belief systems. The naturalist has no room for a creator and the creationist
has no room for anti-Biblical naturalism. In my view neither are ultimately ’science’,
but are, as Popper said of evolution, metaphysical frameworks.
ReMine assumes the ’Big Bang’ cosmology. I initially gave him the benefit
of the doubt here—many creationists just use the ’Big Bang’ as
agreed evidence of a beginning; that everything had a beginning and therefore there
was a ’First Cause’. Many theistic philosophers have taken this approach:
’OK, you accept the Big Bang, you must accept that there was a beginning and
everything which has a beginning has a cause—ultimately the uncaused cause’.
This is fair enough, as far as it goes, but ultimately it entails acceptance of
the evolutionary time-scale with its attendant billions of years of fossil record
and death and suffering before the Fall, and therefore undermines the Gospel which
depends upon the historicity of the Fall and its consequences (I Corinthians 15:21,22).
ReMine, oddly, calls Big Bang cosmology among our ’most firmly established
science’ (p. 467).
ReMine proposes that the fossil sequence—the pattern of abrupt appearance
and the sufficient completeness of the fossil record—was planned by the biotic
message sender (Chapter 21: Fossil sequence and message theory). He proposes that
the message sender did this to thwart the ’life from space’ and other
naturalistic scenarios. This is fanciful. ReMine shows here that he is confused
about the message sent by the message sender in the form of the written Word. The
Bible is clear that death, disease and suffering resulted from the cursing of the
creation after Adam and Eve sinned (Genesis 3, Romans 8). ReMine seems to accept
the fossil dating scheme of the evolutionists without question, which then puts
the death, disease and suffering implied by the fossils before the Fall. The Bible
gives a reason for most of the fossils: the great Flood (Genesis 6–8). The
fossils do send a message; a message of judgment (2 Peter 3). It’s a shame
that ReMine’s otherwise sound logic falls apart here.
It is curious that ReMine begins this chapter with an interesting quote from Raup:
’One of the ironies of the evolution-creation debate is that the creationists
have accepted the mistaken notion that the fossil record shows a detailed and orderly
progression and they have gone to great lengths to accommodate this "fact"
in their Flood geology’ (p. 423).
And then ReMine omits any reference to Flood geology—which can explain the
general patterns seen in the fossils without resorting to the contrivance of planned
sequential release of newly-created organisms. It’s sad that ReMine resorts
to this ’progressive creationist’ approach. It mars an otherwise very
Another negative is the lack of illustrations. There is not one illustration in
this large book of 538 quarto pages. Many of the points made would be made much
clearer with illustrations—for example, the systems of classification, including
’discontinuity systematics’, could be explained much better with diagrams.
There is a lot of unnecessary white space throughout the book which could be put
to good use with some illustrations, or removed to save paper.
It is sad that the book is relatively expensive, which will limit its accessibility
to tertiary science students, who would benefit greatly from this book, particularly
in developing their critical thinking skills regarding origins.
The evolutionary literature is thoroughly reviewed and critiqued. ReMine understands
evolutionary theory better than most evolutionists. The book will inspire those
who read it that biology only makes sense in the light of creation.There is a good
index. Cited references are set out in a single reference index at the end, and
footnotes are used extensively to explain or cross-reference (which is much easier
for the reader than having endnotes, or worse, notes listed by chapter at the end
of the book). There are two helpful and extensive appendices dealing with natural
selection and Haldane’s dilemma in more detail. The volume is beautifully
produced with good quality paper and binding.
This is a book that should be read by anyone interested in the big picture, and
especially biology. It is a landmark volume with many original insights—only
some of which have been touched upon in this review.
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