s 6 s
Theories on Rapid Evolution
"Gaps"
The
observation that new forms and structures appear suddenly in the fossil record
is old news. The difficulty posed by
"missing links" or "gaps" in the fossil record was
acknowledged even by Darwin himself:
Why then is not every geological
formation and every stratum full of such intermediate links? Geology assuredly does not reveal any such
finely graduated organic chain; and this, perhaps, is the most obvious and gravest
objection which can be urged against my theory.
The explanation lies, as I believe, in the extreme imperfection of the
geological record.[1]
Darwin thought the gaps in the
fossil record exist because the record is incomplete, and that subsequent
discoveries might fill in the gaps. To a
degree, he was right. Since then, some
gaps have been replaced by thin bridges of intermediary forms. Yet even where these bridges connect forms in
a parent-descendent relationship, the pattern of sudden appearances, or rapid
transformation into new forms, has not changed.
After 150 years of new discoveries, the pattern is firmly established
and recognized. As Clarkson asserted,
What is seen in the rocks is not
the result of the fossil record's inadequacy, but a fair picture of the actual
pattern of events.[2]
Even George Gaylord Simpson, who
championed the Darwinian opinions of the Modern Synthesis, candidly admitted
the problem,
It is a feature of the known
fossil record that most taxa appear abruptly.
They are not, as a rule, led up to by a sequence of almost imperceptibly
changing forerunners such as Darwin believed should be usual in evolution.[3]
These so-called "gaps"
in the fossil record are a timeless centerpiece of creationist arguments. As Eldredge and Gould put it,
The rarity of transitional series
remains as our persistent bugbear. From
the reputable claims of a Cuvier or an Agassiz to the jibes of modern cranks
and fundamentalists, it has stood as the bulwark of anti-evolutionist
arguments.[4]
Yet by emphasizing the
"gaps," the creationists de-emphasize the fossil links that have been
found, thereby only giving half the picture.
Evolutionist Robert Carroll gave a more complete picture by
acknowledging the pattern of suddenness, yet also making a case for
evolutionary change where evidence exists for it. With regard to sudden appearances, he stated,
Instead
of showing gradual and continuous change through time, the major lineages
appear suddenly in the fossil record.[5]
The same
basic evolutionary pattern applies to all groups for which there is an adequate
fossil record.[6]
New
discoveries are unlikely to change our general understanding of large scale
patterns of evolution.[7]
Instead of new families, orders,
and classes evolving from one another over long periods of time, most had
attained their most distinctive characteristics when they first appeared in the
fossil record and have retained this basic pattern for the remainder of their
duration.[8]
Yet Carroll also found
examples of gradual evolution in conformity with Darwinian expectations. He described the gradual and directional
evolution of ichthyosaur paddles over their 100 million year tenure, as well as
gradual and directional changes in mammal teeth during the Pliocene.[9] He also proposed that late Jurassic pleurosaurs
evolved gradually from the late Triassic sphenodontids.[10]
Likewise, Levinton also acknowledged a "morphological
discontinuity among taxa,"[11]
yet, like Darwin, postulated, "missing data, rather than saltations
(leaps), are the likely explanations."[12]
Even
Gould, who was usually on the opposite side of the fence from the gradualists,
acknowledged a documented case wherein gradual speciation had occurred over a
period of 2 million years from one species of Melanopsis to another.[13]
Thus, although many evolutionists admit that there are
"gaps" in the fossil record, this does not by itself justify
creationists' attempts to use their words to attack evolution, nor to support
the notion that God formed each species as an unrelated lineage, as Genesis 1
repeatedly insists, "each after its own kind."[14] Although there are "gaps" in some
cases, gradual evolution certainly does happen in other cases.
Higher Taxa
The
anomaly has always been, and still remains, the sudden origin of the higher
taxa. As Clarkson put it,
The links between higher taxa are
obscure, and are but poorly represented in the fossil record… but what the
fossil record does give us is many examples of the 'instantaneous' origin of
new structural plans… the origination of higher taxa, in this sense, remains
the least understood of paleontological phenomena.[15]
The
phrase "higher taxa" refers to the broader groupings of life
forms. For example, mammals, birds, and
reptiles are higher taxa than cows, pigeons, and alligators.
From
lower to higher taxa, humans are classified as
·
sapiens
(species) – (lowest)
·
Homo
(genus - plural is genera)
·
Hominids
(family)
·
Primates
(order)
·
Mammals
(class)
·
Chordates
(phylum – plural is phyla)
·
Animals
(kingdom) – (highest)
With
regard to human evolutionary lineage, the lower taxa show a pattern of gradual
transitions, for there are a multitude of fossils that are progressively more
and more human-like and less and less ape-like, which demonstrate human
evolution happened gradually. However,
at the higher taxa, the order primates appeared suddenly, without a gradual
line of fossils connecting it to an earlier group of mammals. It is this puzzle, the origin of higher taxa,
which has proven the most difficult question.
Saltation
Natura non facit saltum. "Nature does not make sudden
leaps." That statement is among the most sacred
scriptures of Darwinism. But during the
first half of the 20th century, a large group of evolutionists
adopted a theory named after the word saltum,
meaning "sudden leaps." Called "Saltationists," they
defied Darwin, asserting that Natura
facit saltum – "Nature does make
sudden leaps." An evolutionist named Schindewolf was
among their proponents. Schindewolf
expressed the conviction that gaps in the fossil record would remain regardless
of whatever new discoveries are made:
The missing links of the cliché
have never been found… the closed evolutionary lineages which we have before us
regularly break off as we near their roots.
Nothing in the future will change this.[16]
Schindewolf pointed out that when
dramatically different life forms first appear in the fossil record, they
cannot be traced to known ancestors by small incremental steps of evolutionary
change. Rather, they appear suddenly, as
"large evolutionary steps, without connecting transitional links."[17] The clean break in the traceability of
ancestry is most acute at the root of the higher taxa:
All decisive transformations of
the basic structures of the higher-ranking types are brought about in large,
individual steps with far-reaching consequences, without links or transitions,
in early ontogenetic stages.[18]
The
beginnings of Saltationism can be traced to Hugo DeVries who lived at the turn
of the 20th century.[19] At the core of Saltationist theory is the
notion that sudden macro-mutational events can radically alter the DNA
sequences of reproductive cells, thus causing a very speedy injection of new
genetic material, the result of which is a new species. In other words, your sperm 'n' eggs get
zapped so hard by some sort of excessive radiation that your kids are born as
mutants. Then, by means of
multi-generational inbreeding, your kids procreate a new and better
species. Another Saltationist,
Goldschmidt, dubbed these hypothetical mutants "hopeful
monsters." The idea is that a
macro-mutation, which is not immediately lethal, could conceivably be tweaked
by natural selection over a few generations into something useful.
Saltationism
is so reviled among some evolutionists that it is called
"heresy." It is now dead and
buried somewhere in the intellectual trash pile of the scientific community,
mostly on account of its genetic impossibilities. The
large-scale genetic mutations it requires are too harmful for the production of
viable mutants. Evolutionary genetics
favors slight mutations, not macro-mutations.
Yet despite
the collapse of Saltationism, the paleontological observations which originally
constituted the basis for it have not gone away.
Punctuated Equilibrium
After
the conventional wisdom of the Darwinists had silenced the Saltationists, it
was just a matter of time before a new theory of rapid evolution was formulated
to explain the sudden appearance of new forms.
In 1972, Niles Eldredge and Stephen Jay Gould published such a
theory. It has gone down in history as
Punctuated Equilibrium, and it remains the most widely held theory of rapid
evolution today.
The
two words, "Punctuated" and "Equilibrium," refer to two
separate phases within the lifetime of a given species. In the first phase, the evolution of a
species is "Punctuated" – meaning that most of the evolutionary change
occurs over a short time period. Second,
there is a long period of relatively little change, called
"Equilibrium" or "stasis."
As Eldredge and Gould put it,
Most evolutionary changes in
morphology occur in a short period of time relative to the total duration of
the species.[20]
One
example of Punctuated Equilibrium in action was provided by a study of African
mollusks from the Turkana Basin. 3,300
individual mollusks across 13 different lineages were measured. Williamson concluded,
The Turkana Basin sequence
clearly conforms to the punctuated equilibrium model: long-term stasis in all
lineages is punctuated by rapid episodes of phenotypic change. No gradualistic morphological trends occurred
in any lineage.
When change did happen,
speciation events were completed within 5,000 to 50,000 years.[21]
Punctuated
Equilibrium can also be observed in the Huaqiao Formation in Hunan, China. Layers of rock record the sudden arrival of
half-a-dozen or so new species, which exist for a while before being replaced
by other suddenly emerging species.
Cycles of spontaneous arrival of new species happen several times in the
formation.[22]
Another
documented occurrence of Punctuated Equilibrium in the fossil record comes from
the analysis of 14,000 conodonts over 10 million years of Ordovician time in
Argentinean strata. Albanesi and Barnes
found that stasis had been punctuated by a brief period of speciation from one
type of tooth-like structure to another.
They hypothesized that the cause of the speciation was genetic isolation
coupled with deposits of volcanic ash into the conodont's habitat. Within 230 meters of rock, there was no
change; then, in less than one meter, the transformation from one type of dentical
to another was complete – representing a period of 50,000 to 100,000
years. This was correlated to Gould's
earlier estimate that marine invertebrate species usually last for 5 to 11
million years, and that the punctuation phase of their evolution generally
accounts for only 1% of that time,[23]
which pleasantly agrees with the 50,000 to 100,000 years they calculated for
the time in which the punctuation event occurred.[24]
The
50,000 to 100,000 years that they calculated for the time it took one species
to evolve into another is consistent with the findings of other studies. Geary's study of Miocene gastropods suggested
that a punctuation event that led to speciation happened in "tens of
thousands of years."[25] Goodfriend and Gould found that the pulmonate
genus Cerion morphed from one species
into another in no more than 15,000 to 20,000 years.[26] Therefore, Punctuated Equilibrium supposes
that evolution happens in the tens of thousands, not millions, of years. Although considerably shorter than
traditional Darwinists suppose, tens of thousands of years is not exactly the
six days mentioned in Genesis 1.
Punctuated Equilibrium cannot support creationist suppositions.
Some
evolutionists were angered by the theory of Punctuated Equilibrium, not so much
because of its scientific merit, but rather because it was presented as an
alternative to Darwinism, which inadvertently resulted in creationists
presenting it as evidence against evolution in general – an unwelcome
consequence that Eldredge and Gould tried to mitigate.
Stasis is Data
The
primary pillar for the theory of Punctuated Equilibrium is the reality of
stasis in the fossil record. Species
tend to remain essentially unchanged for long periods of time, often extending
for millions or even tens of millions of years without altering their
anatomy. As Gould put it,
Stasis is data… The fossil record
may, after all, be 99 percent imperfect, but if you can, nonetheless, sample a
species at a large number of horizons well spread over several million years,
and if these samples record no net change, with beginning and end points
substantially the same, and with only mild and errant fluctuation among the
numerous collections in between, then a conclusion of stasis rests on the presence of data, not on absence![27]
Gould documented a multitude of
examples of stasis, wherein a large number of individual fossils within a
species, sampled over long time increments, revealed a picture of relatively
little or no net change. Gould
summarized evidence for stasis from a large variety of fossilized life forms –
trilobites, beetles, lungfish, cheilostomes, scallops, brachiopods, and certain
ungulates such as wildebeasts.[28] Some of these examples of stasis are based on
extraordinarily plentiful data. For
example, stasis is the norm among nearly all of the more than 330 invertebrate
species that existed over a period of 9 million years in the Devonian times of
the Appalachian Mountains.[29] Some might say these were merely fossilized
hillbillies that were incapable of evolution; notwithstanding, the shear multitude
of data points among these Appalachians is a good indication of the reality of
stasis.
Stasis
is the "equilibrium" part of Punctuated Equilibrium, and often it is
the only part of a species' evolutionary history that can be observed, because
the period of stasis is so much longer than the period of punctuation, that
only fossils from the period of stasis have been preserved.
Richard
Dawkins, a critic of Punctuated Equilibrium, attributes punctuations to
migrations, not to rapid evolution:
When we look at a series of
fossils from any one place, we are probably not looking at an evolutionary event at all: we are
looking at a migrational event, the
arrival of a new species from another geographical area.[30]
However, the difference between a
migrational event and a punctuational event can be distinguished when the
punctuational event has fossil intermediaries in a formation. In fact, Eldredge's first discovery of a punctuation
event was characterized by just that – parent and child species, together with
intermediaries, all in a single formation.
He found that a certain species of trilobite called Phacops milleri dominated lower Hamilton formations for 3 or 4
million years. It consistently had 18
columns of lenses in its eyes. The
entire time period with regard to P.
milleri was characterized by a "simple lack of change."[31] Then, very abruptly, that trilobite was
replaced by another very similar trilobite called Phacops rana, which remained unchanged for 7 or 8 million years
thereafter.[32]
The
replacement was too abrupt, and the periods of stasis too long, for a gradual
transition to be possible. At first,
there were no intermediaries, and so Eldredge, like Dawkins, attributed the
phenomenon to migration, not macromutation.
However, there was one formation in New York, where intermediary forms
did exist. They were present in a
quarry, and occurred enough to discern that the evolutionary event was
completed in just 1,000 to 10,000 years' time.[33] Once the change was complete, the new species
branched out to new locations, replacing the earlier species, and it remained
essentially unchanged for millions of years thereafter.
We
may draw certain conclusions from Punctuated Equilibrium. Among them,
1. Species stay essentially
unchanged for millions of years.
2. When species do evolve, they
evolve within thousands of years, not millions.
3. The degree to which they evolve
is small and produces only a slightly different descendent species.
The Problem Remains
This
third conclusion, namely that Punctuated Equilibrium explains only small
evolutionary changes, should draw our attention, for it means that Punctuated
Equilibrium does not necessarily solve the bigger problem regarding the sudden
appearance of higher taxa. This, I
think, should give us pause, for it tends to limit the applicability of
Punctuated Equilibrium to the level of the lower taxa, and leaves us still
curious about the higher taxa. Eldredge
himself hinted at the matter, speaking about Phacops rana,
Hardly prodigious, this degree of
anatomical retooling falls well within the bounds of
"micro-evolution" – loosely speaking, the kind and degree of
relatively minor change that marks the difference between closely related
species.[34]
The
sudden appearance of new and completely unparalleled forms is the great
problem. Where are the missing links
from archosaurs to pterosaurs? From
mustelids to sea lions? From Ediacaran
fauna to the Cambrian Explosion?
Punctuated Equilibrium seems to only address small changes from species
to species – not from order to order, class to class, or phylum to phylum, and
therefore does not answer the most pressing question about the origin of higher
taxa. The examples of Punctuated
Equilibrium that can be garnered from the fossil record – the snails, the
conodonts, the trilobites – all these are examples of minor species-level
changes. Although Punctuated Equilibrium
is an excellent framework for explaining small evolutionary changes at the
level of the lower taxa, it is not necessarily directly pertinent to the bigger
problem regarding the sudden appearance of higher taxa.
If
the change brought from a punctuation event is small, as every indication
testifies, then an accumulation of Punctuated Equilibrium cycles are required
before a quantum leap from one phylum, class, or order can be realized. And if these punctuations are most often
separated by long periods of stasis, then would not the emergence of new phyla,
classes, and orders be, as a matter of the big picture, gradual?
The
accomplishments of multiple Punctuated Equilibrium cycles over time should
therefore yield a gradual advancement not too different from what Darwin
originally envisioned – a slow and steady progress, characterized by
punctuations, yes, but each of such a small scale and with such infrequency as
to be barely distinguishable from the "big picture" of phyletic
gradualism. The alternation between
stasis and punctuation yields a very slow rate of progress over time. It still falls short of explaining the sudden
emergence of the higher taxa. For even
though a punctuation at the level of species or genus, such as Phacops was, could be quite speedy;
however, the subsequent period of stasis is not speedy, and therefore if we
wish to use the framework of Punctuated Equilibrium to explain, for example,
how the trilobite's relatives became spiders, we must assume it happened over a
long period of time, for a large number of punctuations followed by periods of
stasis must have occurred to make it happen.
The
three figures below plot amounts of evolution over time. Notice that both Darwinism and Punctuated
Equilibrium yield an overall pattern of gradual evolution. Even though Punctuated Equilibrium is
characterized by fits and starts, it still necessarily takes a long time to
accomplish significant evolutionary change at the magnitude of higher
taxa. That is because stasis separates
punctuations, and because punctuations only accomplish small amounts of change. Both traditional Darwinism and Punctuated
Equilibrium contrast sharply with what the fossil record actually demands, for
the fossil record frequently does not allow for the gradual evolution of higher
taxa.



However,
if we postulate that several punctuations occurred in rapid succession, then
perhaps we have an answer. For if the
punctuations were very numerous and followed each other in quick succession,
occurring with greater frequency, and with shorter periods of stasis
intervening between them, this might explain the sudden appearance of the
higher taxa. We might call it "Punctuated Punctuationalism," in which
the "Equilibrium" part of the process is skipped or greatly
abbreviated. If this model works in
tandem with Punctuated Equilibrium, then rapid succession of punctuations is followed
by long periods wherein punctuations are comparatively infrequent. If this is the case, we might interpose a
staircase upon the quantum leap, such that sudden leaps are explained by the
summation of smaller punctuation events.
A graphical example is below.

Yet
for this to happen, one must consider the series of population bottlenecks that
would follow each punctuation event, for the bottlenecks would rapidly deplete
the gene pool and make species vulnerable to further selective pressures. As with the case of the dark and light
colored moths mentioned earlier, the more selection kills off the ill-adapted
members of a species, the more that species looses its genetic variety. The more it looses its variety, the less able
it is to make further adaptations.
Moreover,
every time a species is nearly killed off in a bottleneck, the population
declines, which significantly increases the chances of inbreeding. This brings harmful recessive alleles to the
surface, where they kill their carriers and thus exterminate even more variety
from the gene pool. The mutations that
enable evolution to occur get killed off before transposable elements can
reshuffle them and make them useful.
The
question is, can the mechanics of population genetics support a series of
population bottlenecks associated with several punctuations in rapid
succession, and still retain enough genetic variety to effect a
mega-evolutionary transition on the order of magnitude required to explain the
sudden appearance of higher taxa?
Yet
even if it were genetically plausible, we are still left with another question
– what caused the series of punctuations in rapid succession to begin with?
[1] Darwin, Charles. On the Origin of Species by Means of Natural Selection. 1859, p 280
[2] Clarkson, E N K. Invertebrate Paleontology and Evolution, 2nd Edition. 1986, Unwin Hyman Ltd, London, UK, p 26
[3] Simpson, George Gaylord. In Tax, S. Evolution After Darwin. 1960, University of Chicago Press, Chicago, IL, p 149
[4] Eldredge, Niles; Gould, Stephen Jay. Punctuated Equilibrium: An Alternative to Phyletic Gradualism. First published in 1972, Models of Paleobiology, Edited by T J M Schopf. Reprinted in Eldredge, Niles. Time Frames: The Rethinking of Darwinian Evolution and the Theory of Punctuated Equilibrium. 1985, Simon and Schuster, New York, NY, p 198-199
[5] Carroll, Robert L. Patterns and Processes of Vertebrate Evolution. 1997, Cambridge University Press, Cambridge, UK, p 2
[6] Carroll, Robert L. ibid, p 8
[7] Carroll, Robert L. ibid, p 16
[8] Carroll, Robert L. ibid, p 167
[9] Carroll, Robert L. ibid, p 257, 90-95
[10] Carroll, Robert L. ibid, p 473-475
[11] Levinton, Jeffrey S. Genetics, Paleontology, and Macroevolution. 2001, Cambridge University Press, Cambridge, UK, p 208
[12] Levinton, Jeffrey S. ibid, p 357
[13] Gould, Stephen Jay. The Structure of Evolutionary Theory. 2002, President and Fellows of Harvard College, The Belknap Press of Harvard University Press, Cambridge, MA, p 867
[14] Genesis 1:11-12, 1:21, 1:24-25
[15] Clarkson, E N K. Invertebrate Paleontology and Evolution, 2nd Edition. 1986, Unwin Hyman Ltd, London, UK, p 37-38
[16] Schindewolf, Otto H. Basic Questions in Paleontology. 1950, E Schweizerbartsche Verlagsbuchhandlung, Erwin Nagele, Stuttgart, Germany. Translated by Schaefer, Judith. Edited by Reif, Wolf-Ernst, Forward by Gould, Stephen Jay. 1993, The University of Chicago Press, Chicago, IL, p 106
[17] Schindewolf, Otto H. ibid, p 124
[18] Schindewolf, Otto H. ibid, p 211
[19] Schwartz, Jeffrey H. Sudden Origins. 1999, John Wiley & Sons Inc, USA, p 192
[20] Eldredge, Niles; Gould, Stephen Jay. Punctuated Equilibrium: An Alternative to Phyletic Gradualism. First published in 1972, Models of Paleobiology, Edited by Schopf, T J M. Reprinted in Eldredge, Niles. Time Frames: The Rethinking of Darwinian Evolution and the Theory of Punctuated Equilibrium, 1985, Simon and Schuster, New York, NY, p 204
[21] Williamson, P G. Paleontological Documentation of Speciation in Cenozoic Molluscs from Turkana Basin. 1981, Nature 293, p 437-443
[22] Peng, Shanchi; Robison, Richard A. Agnostoid Biostratigraphy Across the Middle-Upper Cambrian Boundary in Hunan, China. 2000, Journal of Paleontology, Volume 74, Special Issue 53, p 4
[23] Gould, Stephen J. The Meaning of Punctuated Equilibrium and Its Role in Validating a Hierarchical Approah to Macroevolution. Compiled in Milkman, R. Perspectives on Evolution. 1982, Sinauer, Sunderland, MA, p 83-104; and in The Structure of Evolutionary Theory. 2002, President and Fellows of Harvard College, The Belknap Press of Harvard University Press, Cambridge, MA, p 768
[24] Albanesi, Guillermo L; Barnes, Christopher R. Subspeciation Within a Punctuated Equilibrium Evolutionary Event: Phylogenetic History of the Lower-Middle Ordovician Paroistodus Originalis-P. Horridus Complex (Conodonta). 2000, Journal of Paleontology 74(3), p 492-502
[25] Geary, D H. The Importance of Gradual Change in Species-Level Transitions. In Erwin, D H; Anstey, R L. New Approaches to Speciation in the Fossil Record. 1995, Columbia University Press, NY, p 67-86
[26] Goodfriend, G A; Gould, S J. Paleontology and Chronology of Two Evolutionary Transitions by Hybridization in the Bahamian Land Snail Cerion. 1996, Science 274, p 1894-1897
[27] Gould, Stephen Jay. The Structure of Evolutionary Theory. 2002, President and Fellows of Harvard College, The Belknap Press of Harvard University Press, Cambridge, MA, p 759
[28] Gould, Stephen Jay. ibid, p 753-755, 769, 788, 817, 824, 826, 866; and references therein
[29] Gould, Stephen Jay. ibid, p 865
[30] Dawkins, Richard. The Blind Watchmaker: Why the Evidence of Evolution Reveals a Universe without Design. 1987, W W Norton & Company, New York, NY, London, UK, p 240
[31] Eldredge, Niles. Time Frames: The Rethinking of Darwinian Evolution and the Theory of Punctuated Equilibrium, 1985, Simon and Schuster, New York, NY, p 67-70
[32] Eldredge, Niles. ibid, p 80
[33] Eldredge, Niles. ibid, p 81
[34] Eldredge, Niles. ibid, p 70