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509 of 682 people found the following review helpful:
2.0 out of 5 stars
Mostly dreadful, but some good points., June 12, 2007
In the Debacle in Dover, testifying about biochemistry, his main area of expertise, Behe frequently looked like a complete ID-iot. In EOE, Behe spends substantial time discussing areas outside his main ariea of expertise: zoology, astrophysics, developmental biology, etc. Question: If Behe couldn't survive cross-examination in his main area of expertise, then why should we trust him about other areas?
Besides that troubling, general question, there are several specific items that indicate that Behe simply cannot be trusted to get his facts straight. While some reviewers have identified some fairly esoteric errors, I would like to highlight more basic errors, errors so fundamental that a reasonably knowledgeable high school student would catch them.
Behe claims that his previous book, "Darwin's Black Box" (DBB), showed that irreducibly complex (IC) systems could not possibly have evolved in a step-by-step manner, but in reality DBB never said any such thing. DBB argued only that "direct" evolution was highly unlikely. Not only does that still leave the door open for "indirect" evolution, but "highly unlikely" is obviously not the same thing as "impossible." A reasonably sharp high school student would recognize both of those serious errors.
Behe also has a nasty habit of moving the goalposts on an ad hoc basis. In DBB, Behe claimed that IC systems met the standard set by Darwin himself: "could not possibly have been formed by numerous, successive, slight modifications." Under that standard, which Behe freely accepted, merely plausible evolutionary pathways would be effective rebuttals of Behe's IC claims; but whenever biologists mention the numerous, plausible pathways that exist, Behe suddenly changes the standard to "rigorous, detailed explanations." Even a high school student would recognize that "rigorous, detailed explanations" is a radically different standard from "plausible." Such glaring inconsistency on such a key point seems to imply deliberate deception.
Some of Behe's statistical arguments assume that evolutionary success involves finding a needle in a haystack, i.e., a single, specific combination of mutations. In reality, as Behe himself implies in discussing the "Red Queen" effect, there is frequently a large, possibly enormous, number of potentially beneficial combinations available; so evolution is not searching for a needle, rather it is searching for a haystack; and therefore the odds of success are enormously greater than Behe's statistics imply. Any reasonably sharp high school student would recognize the glaring flaw in Behe's deceptive statistics.
Creationists with limited math abilities seem greatly impressed even by math arguments as obviously stupid as Behe's. I think it's worthwhile to point out that the most influential statistician of the 20th century was probably Sir Ronald Fisher, who, in addition to his spectacular achievements in statistics, also happens to have been one of the most influential evolutionists of the 20th century, having been one of the principal proponents of the "modern synthesis." So when ID-iots like Behe start bloviating about statistics, just remember that the real expert in statistics, Sir Ronald Fisher, was an evolutionist.
Finally, in another key argument, Behe simply assumes that "fitness landscapes" never change, but anyone with even a high school level knowledge of earth science knows that physical landscapes change all the time, due to floods, earthquakes, erosion, etc. Is Behe really so clueless that he doesn't realize that if physical landscapes change, then "fitness landscapes" must change too? Behe's idea of an organism "trapped on a fitness peak," forever barred from crossing even a shallow valley and thereby potentially gaining access to a even higher peak is so obviously stupid that any reasonably knowledgeable high school student would reject it.
I fully realize that not everyone can catch every error. Even major errors, like some of those pointed out by other critics, might slip by if they involve obscure or highly technical details. But it is really baffling that five-star reviewers blithely overlook numerous, major blunders that any knowledgeable high school student would catch. How in God's name could that happen?
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795 of 1,151 people found the following review helpful:
1.0 out of 5 stars
The Edge of Inanity: The Search for the Limits of Credulity, June 6, 2007
Behe's all dog no pony Irreducible Complexity (IC) tour is back in town - fresh from a Dover, PA appearance where he literally brought down the house of Intelligent Design (ID) cards with a slapstick vaudeville routine that confusingly conflated astrology with astronomy, dismissed reams (literally) of research into the evolution of the blood clotting cascade, and routinely produced 'oh dear' deer in the headlights stares while under cross examination.
Much of "The Edge of Evolution" centers on the purported inability of evolutionary mechanisms to account for parasites such as malaria. Behe's preferred instrument of faith-based flagellation - the flagellum - stages an encore performance as the malarial cilium; which to Behe's doe eyes looks even more IC than it did before.
Research is cited to show that the production of cilium in eukaryotic cells depends upon the availability of another cellular system known as intraflagellar transport (IFT). Behe then asserts (as in provides no supporting evidence) that both the cilium and IFT are irreducibly complex - in fact he christens this section "Irreducible Complexity Squared" (note to the Discovery Institute: get that trademark application in soon, how about IC2). Behe writes on page 94:
"IFT exponentially increases the difficulty of explaining the irreducibly complex cilium. It is clear from careful experimental work with all ciliated cells that have been examined, from alga to mice, that a functioning cilium requires a working IFT. The problem of the origin of the cilium is now intimately connected to the problem of the origin of IFT. Before its discovery we could be forgiven for overlooking the problem of how a cilium was built. Biologists could vaguely wave off the problem, knowing that some proteins fold by themselves and associate in the cell without help. Just as a century ago Haeckel thought it would be easy for life to originate, a few decades ago one could have been excused for thinking it was probably easy to put a cilium together; the piece could probably just glom together on their own. But now that the elegant complexity of IFT has been uncovered, we can ignore the question no longer."
IC2 states that you can't have/build/produce cilia without a functioning IFT mechanism - evolutionary (natural) causations must explain the apparently choreographed origin of IFT and the origin of cilia - quod erat demonstrum. Unfortunately this claim is false. In the real world eukaryotes exist which have cilia but lack IFT.
One of these organisms belongs to a group called Apicomplexans. These protozoa are obligatory intracellular parasites that must spend part, if not all, of their life cycle in a host animal. The specific apicomplexan in question is Plasmodium falciparum. You probably know it better by its street name: malaria. The organism that Behe touts throughout as being an intelligently designed exemplar of irreducibly complex systems completely demolishes his entire claim that cilia and IFT constitute an irreducible system - squared or not.
Compounding the Plasmodium falciparum debacle is Behe's rubber-band reality utilization of fitness landscape arguments in a chapter that should have been titled "The Mathematical Limits of Beheism" since it only manages to showcase his profligate innumeracy. Here's how Behe turned a fitness landscape into a swamp (with thanks to Mark Chu-Carroll):
1. Restrict evolution to a static and unchanging fitness landscape - unfortunately in the real world fitness landscapes are never static. 2. Constrain the fitness landscape to a smooth surface made up of hills and valleys where a local minimum or maximum in any dimension is a local minimum or maximum in all dimensions - and ignore that a valley in one dimension can be a peak in another. 3. Assert that fitness function mapping from a genome to a point of the fitness landscape is monotonically increasing - in spite of the fact that things don't always go in a single direction - for example a virus may decrease in fitness over time but increase in transmissibility. 4. Define the fitness function as smoothly continuous, with infinitesimally small changes (single point base changes) mapping to equally small changes in position on the fitness landscape - in spite of experimental evidence that even a single base pair change (in a viral quasispecies for example) can eliminate one peak while creating another (and also ignore the consequences of gene duplication, recombination, insertional mutations, transposition, and translocation).
As Mark points out Behe doesn't even understand that he is making these assumptions - you can wade through his mathematics without getting your ankles wet. He then traipses into quicksand of his own design by basing all of his arguments on the flawed fitness landscape and straightjacketed search results they produce. William Dembski acted as an advisor to Behe - and it shows. The master of obscurantist pseudomathematics has found a willing apprentice.
Transmuting lush fitness landscapes into malarial swamps is quite a trick but Behe, ever the prankster, isn't finished yet. Behe accepts common descent and admits that overwhelming evidence links closely related species (e.g. humans and chimpanzees) to shared ancestors, but flatly asserts that evolution by natural means is incapable of facilitating genus or taxa level differentiation such as the emergence of tetrapods from Sarcopterygian fish. The horns of this dilemma should be obvious, even to Behe; how can all species be linked by common descent if evolution above the species level is impossible?
Behe never resolves this disconnect - no mechanism is ever offered. No hint of a hypothesis. No suggested experimental avenues. This logical lacuna can't be bridged by incessant appeals to 'design.' Behe further muddies the waters by surreptitiously substituting a concept much closer to creationist 'baramin' (created kinds) for biological species - created kinds and common descent are irreconcilable concepts.
Ultimately Behe's colleagues at Lehigh University are ideally positioned to comment on his work. The Department of Biological Sciences has posted the following statement on their website concerning Behe:
"The faculty in the Department of Biological Sciences is committed to the highest standards of scientific integrity and academic function. This commitment carries with it unwavering support for academic freedom and the free exchange of ideas. It also demands the utmost respect for the scientific method, integrity in the conduct of research, and recognition that the validity of any scientific model comes only as a result of rational hypothesis testing, sound experimentation, and findings that can be replicated by others."
"The department faculty, then, are unequivocal in their support of evolutionary theory, which has its roots in the seminal work of Charles Darwin and has been supported by findings accumulated over 140 years. The sole dissenter from this position, Prof. Michael Behe, is a well-known proponent of 'intelligent design.' While we respect Prof. Behe's right to express his views, they are his alone and are in no way endorsed by the department. It is our collective position that intelligent design has no basis in science, has not been tested experimentally, and should not be regarded as scientific."
Behe's book is one long train wreck. Unlike Darwin who eloquently elucidated one long argument, Behe tosses off sloppy seconds as research, recycles sophomoric (and rejected) fitness landscape arguments, confusingly conflates or redefines common terms and proffers puerile probability assessments - standard creationist (excuse me, I meant to say IDist) fare.
Thanks to Nick Matzke for uncovering Behe's monumentally grotesque Plasmodium falciparum gaffe.
Special thanks as well to Behe's dysfunctional advisory team: Lydia and Tim McGrew, Peter and Paul Nelson, George Hunter, David DeWitt, Doug Axe, Bill Dembski, Jonathan Wells, Tony Jelsma, Neil Manson, Jay Richards, Guillermo Gonzalez, Bruce Chapman, Steve Meyer, John West, and Rob Crowther - a veritable bestiary of methodological supernaturalists operating at the edge of inanity - and only one 's' away from insanity.
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84 of 121 people found the following review helpful:
2.0 out of 5 stars
Good try, but shaky arguments, July 14, 2007
Behe accepts common descent, and therefore by definition evolution. He claims "Darwinian" micro-evolution, but "designed" macro-evolution. He thus argues not for an edge to evolution, but for an edge to natural selection, beyond which we find the intelligent designer. (Though Behe coyly says that the conclusion is really up to the reader; he's only presenting scientific facts.) For reasons not readily apparent to me, he places the boundary or edge somewhere between Orders and Genera. Apparently Behe doesn't realize the ancestors of today's primates and petunias were once in the same Genus, if you go back far enough.
There's much to criticize, so I'll just pick three items.
Behe claims to prove mathematically that the chance of 3 beneficial genetic mutations occuring simultaneously is statistically virtually zero, throughout all the existence of life on earth. Assume that's true, although Behe ignores the good possibility of higher mutation rates under earth's earlier, more radiation-penetrable atmosphere. Still, he hasn't proven that simultaneous, rather than sequential, mutations are necessary to natural selection. (Obviously, the genetic modifications that produced a light-sensitive cell, a lens, an iris, and eyelids didn't occur at once.) However, he states that malaria bacteria resistant to chloroquine may have as many as 8 genetic mutations, developed through random mutation and natural selection. Albeit he claims 2 of the mutations as "primary", yet he says the others "apparently 'compensate' for side-effects" of the primary mutations. So actually Behe cites a case of 8 individual self-reinforcing genetic mutations arising, apparently sequentially. And, these obviously contradictory items occur within 15 pages of each other!
Behe claims that natural selection is always detructive, rather than constructive - it can't add anything "new". In addition to basing this on the "insufficient mutation rate/insufficient chance of accumulation of beneficial mutations" argument above, which Behe himself naively contradicts, he seems to be working with some rather Platonic concept of an abstract "ideal" fitness outside of environment conditions. So Behe seems to suggest that the sickle-cell trait is destructive of the organism's "ideal" fitness. Rather, in a tropic environment, it is constructive precisely because on average you are more likely to live to reproduce if you have the trait.
Irreducable complexity: Since the old favorite the eye has been shown to fail this argument, through the presence of numerous useable forms simpler than the complex human eye, the new candidate Behe puts forward is bacterial cilia. Apparently Behe would ask us to stop trying to seek how this could have evolved naturally, turn from biology to mysticism and theology, and just bow our heads. No doubt if Behe had lived 500 years ago, he'd tell us not to worry what the stars are made of - god put them there, and we'll never know.
Buy this to read the best the ID crowd can produce, and buy Dawkin's Climbing Mount Improbable for your ID-inclined friends.
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