The God Delusion

  So, we have seen that eyes and wings are certainly not irreducibly complex; but what is more interesting than these particular examples is the general lesson we should draw. The fact that so many people have been dead wrong over these obvious cases should serve to warn us of other examples that are less obvious, such as the cellular and biochemical cases now being touted by those creationists who shelter under the politically expedient euphemism of 'intelligent design theorists'.

  We have a cautionary tale here, and it is telling us this: do not just declare things to be irreducibly complex; the chances are that you haven't looked carefully enough at the details, or thought carefully enough about them. On the other hand, we on the science side must not be too dogmatically confident. Maybe there is something out there in nature that really does preclude, by its genuinely irreducible complexity, the smooth gradient of Mount Improbable. The creationists are right that, if genuinely irreducible complexity could be properly demonstrated, it would wreck Darwin's theory. Darwin himself said as much: 'If it could be demonstrated that any complex organ existed which could not possibly have been formed by numerous, successive, slight modifications, my theory would absolutely break down. But I can find no such case.' Darwin could find no such case, and nor has anybody since Darwin's time, despite strenuous, indeed desperate, efforts. Many candidates for this holy grail of creationism have been proposed. None has stood up to analysis.

  In any case, even though genuinely irreducible complexity would wreck Darwin's theory if it were ever found, who is to say that it wouldn't wreck the intelligent design theory as well? Indeed, it already has wrecked the intelligent design theory, for, as I keep saying and will say again, however little we know about God, the one thing we can be sure of is that he would have to be very very complex and presumably irreducibly so!

  THE WORSHIP OF GAPS

  Searching for particular examples of irreducible complexity is a fundamentally unscientific way to proceed: a special case of arguing from present ignorance. It appeals to the same faulty logic as 'the God of the Gaps' strategy condemned by the theologian Dietrich Bonhoeffer. Creationists eagerly seek a gap in present-day knowledge or understanding. If an apparent gap is found, it is assumed that God, by default, must fill it. What worries thoughtful theologians such as Bonhoeffer is that gaps shrink as science advances, and God is threatened with eventually having nothing to do and nowhere to hide. What worries scientists is something else. It is an essential part of the scientific enterprise to admit ignorance, even to exult in ignorance as a challenge to future conquests. As my friend Matt Ridley has written, 'Most scientists are bored by what they have already discovered. It is ignorance that drives them on.' Mystics exult in mystery and want it to stay mysterious. Scientists exult in mystery for a different reason: it gives them something to do. More generally, as I shall repeat in Chapter 8, one of the truly bad effects of religion is that it teaches us that it is a virtue to be satisfied with not understanding.

  Admissions of ignorance and temporary mystification are vital to good science. It is therefore unfortunate, to say the least, that the main strategy of creation propagandists is the negative one of seeking out gaps in scientific knowledge and claiming to fill them with 'intelligent design' by default. The following is hypothetical but entirely typical. A creationist speaking: 'The elbow joint of the lesser spotted weasel frog is irreducibly complex. No part of it would do any good at all until the whole was assembled. Bet you can't think of a way in which the weasel frog's elbow could have evolved by slow gradual degrees.' If the scientist fails to give an immediate and comprehensive answer, the creationist draws a default conclusion: 'Right then, the alternative theory, "intelligent design", wins by default.' Notice the biased logic: if theory A fails in some particular, theory B must be right. Needless to say, the argument is not applied the other way around. We are encouraged to leap to the default theory without even looking to see whether it fails in the very same particular as the theory it is alleged to replace. Intelligent design - ID - is granted a Get Out Of Jail Free card, a charmed immunity to the rigorous demands made of evolution.

  But my present point is that the creationist ploy undermines the scientist's natural - indeed necessary - rejoicing in (temporary) uncertainty. For purely political reasons, today's scientist might hesitate before saying: 'Hm, interesting point. I wonder how the weasel frog's ancestors did evolve their elbow joint. I'm not a specialist in weasel frogs, I'll have to go to the University Library and take a look. Might make an interesting project for a graduate student.' The moment a scientist said something like that - and long before the student began the project - the default conclusion would become a headline in a creationist pamphlet: 'Weasel frog could only have been designed by God.'

  There is, then, an unfortunate hook-up between science's methodological need to seek out areas of ignorance in order to target research, and ID's need to seek out areas of ignorance in order to claim victory by default. It is precisely the fact that ID has no evidence of its own, but thrives like a weed in gaps left by scientific knowledge, that sits uneasily with science's need to identify and proclaim the very same gaps as a prelude to researching them. In this respect, science finds itself in alliance with sophisticated theologians like Bonhoeffer, united against the common enemies of naive, populist theology and the gap theology of intelligent design.

  The creationists' love affair with 'gaps' in the fossil record symbolizes their whole gap theology. I once introduced a chapter on the so-called Cambrian Explosion with the sentence, 'It is as though the fossils were planted there without any evolutionary history.' Again, this was a rhetorical overture, intended to whet the reader's appetite for the full explanation that was to follow. Sad hindsight tells me now how predictable it was that my patient explanation would be excised and my overture itself gleefully quoted out of context. Creationists adore 'gaps' in the fossil record, just as they adore gaps generally.

  Many evolutionary transitions are elegantly documented by more or less continuous series of gradually changing intermediate fossils. Some are not, and these are the famous 'gaps'. Michael Shermer has wittily pointed out that if a new fossil discovery neatly bisects a 'gap', the creationist will declare that there are now twice as many gaps! But in any case, note yet again the unwarranted use of a default. If there are no fossils to document a postulated evolutionary transition, the default assumption is that there was no evolutionary transition, therefore God must have intervened.

  It is utterly illogical to demand complete documentation of every step of any narrative, whether in evolution or any other science. You might as well demand, before convicting somebody of murder, a complete cinematic record of the murderer's every step leading up to the crime, with no missing frames. Only a tiny fraction of corpses fossilize, and we are lucky to have as many intermediate fossils as we do. We could easily have had no fossils at all, and still the evidence for evolution from other sources, such as molecular genetics and geographical distribution, would be overwhelmingly strong. On the other hand, evolution makes the strong prediction that if a single fossil turned up in the wrong geological stratum, the theory would be blown out of the water. When challenged by a zealous Popperian to say how evolution could ever be falsified, J. B. S. Haldane famously growled: 'Fossil rabbits in the Precambrian.' No such anachronistic fossils have ever been authentically found, despite discredited creationist legends of human skulls in the Coal Measures and human footprints interspersed with dinosaurs'.

  Gaps, by default in the mind of the creationist, are filled by God. The same applies to all apparent precipices on the massif of Mount Improbable, where the graded slope is not immediately obvious or is otherwise overlooked. Areas where there is a lack of data, or a lack of understanding, are automatically assumed to belong, by default, to God. The speedy resort to a dramatic proclamation of 'irreducible complexity' represents a failure of the imagination. Some biological organ, if not an eye then a bacterial flagellar motor or a biochemical pathway, is decreed without f
urther argument to be irreducibly complex. No attempt is made to demonstrate irreducible complexity. Notwithstanding the cautionary tales of eyes, wings and many other things, each new candidate for the dubious accolade is assumed to be transparently, self-evidently irreducibly complex, its status asserted by fiat. But think about it. Since irreducible complexity is being deployed as an argument for design, it should no more be asserted by fiat than design itself. You might as well simply assert that the weasel frog (bombardier beetle, etc.) demonstrates design, without further argument or justification. That is no way to do science.

  The logic turns out to be no more convincing than this: 'I [insert own name] am personally unable to think of any way in which [insert biological phenomenon] could have been built up step by step. Therefore it is irreducibly complex. That means it is designed.' Put it like that, and you immediately see that it is vulnerable to some scientist coming along and finding an intermediate; or at least imagining a plausible intermediate. Even if no scientists do come up with an explanation, it is plain bad logic to assume that 'design' will fare any better. The reasoning that underlies 'intelligent design' theory is lazy and defeatist - classic 'God of the Gaps' reasoning. I have previously dubbed it the Argument from Personal Incredulity.

  Imagine that you are watching a really great magic trick. The celebrated conjuring duo Penn and Teller have a routine in which they simultaneously appear to shoot each other with pistols, and each appears to catch the bullet in his teeth. Elaborate precautions are taken to scratch identifying marks on the bullets before they are put in the guns, the whole procedure is witnessed at close range by volunteers from the audience who have experience of firearms, and apparently all possibilities for trickery are eliminated. Teller's marked bullet ends up in Penn's mouth and Penn's marked bullet ends up in Teller's. I [Richard Dawkins] am utterly unable to think of any way in which this could be a trick. The Argument from Personal Incredulity screams from the depths of my prescientific brain centres, and almost compels me to say, 'It must be a miracle. There is no scientific explanation. It's got to be supernatural.' But the still small voice of scientific education speaks a different message. Penn and Teller are world-class illusionists. There is a perfectly good explanation. It is just that I am too naive, or too unobservant, or too unimaginative, to think of it. That is the proper response to a conjuring trick. It is also the proper response to a biological phenomenon that appears to be irreducibly complex. Those people who leap from personal bafflement at a natural phenomenon straight to a hasty invocation of the supernatural are no better than the fools who see a conjuror bending a spoon and leap to the conclusion that it is 'paranormal'.

  In his book Seven Clues to the Origin of Life, the Scottish chemist A. G. Cairns-Smith makes an additional point, using the analogy of an arch. A free-standing arch of rough-hewn stones and no mortar can be a stable structure, but it is irreducibly complex: it collapses if any one stone is removed. How, then, was it built in the first place? One way is to pile a solid heap of stones, then carefully remove stones one by one. More generally, there are many structures that are irreducible in the sense that they cannot survive the subtraction of any part, but which were built with the aid of scaffolding that was subsequently subtracted and is no longer visible. Once the structure is completed, the scaffolding can be removed safely and the structure remains standing. In evolution, too, the organ or structure you are looking at may have had scaffolding in an ancestor which has since been removed.

  'Irreducible complexity' is not a new idea, but the phrase itself was invented by the creationist Michael Behe in 1996.62 He is credited (if credited is the word) with moving creationism into a new area of biology: biochemistry and cell biology, which he saw as perhaps a happier hunting ground for gaps than eyes or wings. His best approach to a good example (still a bad one) was the bacterial flagellar motor.

  The flagellar motor of bacteria is a prodigy of nature. It drives the only known example, outside human technology, of a freely rotating axle. Wheels for big animals would, I suspect, be genuine examples of irreducible complexity, and this is probably why they don't exist. How would the nerves and blood vessels get across the bearing?* The flagellum is a thread-like propeller, with which the bacterium burrows its way through the water. I say 'burrows' rather than 'swims' because, on the bacterial scale of existence, a liquid such as water would not feel as a liquid feels to us. It would feel more like treacle, or jelly, or even sand, and the bacterium would seem to burrow or screw its way through the water rather than swim. Unlike the so-called flagellum of larger organisms like protozoans, the bacterial flagellum doesn't just wave about like a whip, or row like an oar. It has a true, freely rotating axle which turns continuously inside a bearing, driven by a remarkable little molecular motor. At the molecular level, the motor uses essentially the same principle as muscle, but in free rotation rather than in intermittent contraction.t It has been happily described as a tiny outboard motor (although by engineering standards - and unusually for a biological mechanism - it is a spectacularly inefficient one).

  * There is an example in fiction. The children's writer Philip Pullman, in His Dark Materials, imagines a species of animals, the 'mulefa', that co-exist with trees that produce perfectly round seedpods with a hole in the centre. These pods the mulefa adopt as wheels. The wheels, not being part of the body, have no nerves or blood vessels to get twisted around the 'axle' (a strong claw of horn or bone). Pullman perceptively notes an additional point: the system works only because the planet is paved with natural basalt ribbons, which serve as 'roads'. Wheels are no good over rough country.

  Fascinatingly, the muscle principle is deployed in yet a third mode in some insects such as flies, bees and bugs, in which the flight muscle is intrinsically oscillatory, like a reciprocating engine. Whereas other insects such as locusts send nervous instructions for each wing stroke (as a bird does), bees send an instruction to switch on (or switch off) the oscillatory motor. Bacteria have a mechanism which is neither a simple contractor (like a bird's flight muscle) nor a reciprocator (like a bee's flight muscle), but a true rotator: in that respect it is like an electric motor or a Wankel engine.

  Without a word of justification, explanation or amplification, Behe simply proclaims the bacterial flagellar motor to be irreducibly complex. Since he offers no argument in favour of his assertion, we may begin by suspecting a failure of his imagination. He further alleges that specialist biological literature has ignored the problem. The falsehood of this allegation was massively and (to Behe) embarrassingly documented in the court of Judge John E. Jones in Pennsylvania in 2005, where Behe was testifying as an expert witness on behalf of a group of creationists who had tried to impose 'intelligent design' creationism on the science curriculum of a local public school - a move of 'breathtaking inanity', to quote Judge Jones (phrase and man surely destined for lasting fame). This wasn't the only embarrassment Behe suffered at the hearing, as we shall see. The key to demonstrating irreducible complexity is to show that none of the parts could have been useful on its own. They all needed to be in place before any of them could do any good (Behe's favourite analogy is a mousetrap). In fact, molecular biologists have no difficulty in finding parts functioning outside the whole, both for the flagellar motor and for Behe's other alleged examples of irreducible complexity. The point is well put by Kenneth Miller of Brown University, for my money the most persuasive nemesis of 'intelligent design', not least because he is a devout Christian. I frequently recommend Miller's book, Finding Darwin's God, to religious people who write to me having been bamboozled by Behe.

  In the case of the bacterial rotary engine, Miller calls our attention to a mechanism called the Type Three Secretory System or TTSS.63 The TTSS is not used for rotatory movement. It is one of several systems used by parasitic bacteria for pumping toxic substances through their cell walls to poison their host organism. On our human scale, we might think of pouring or squirting a liquid through a hole; but, once again, on the bacterial scale thin
gs look different. Each molecule of secreted substance is a large protein with a definite, three-dimensional structure on the same scale as the TTSS's own: more like a solid sculpture than a liquid. Each molecule is individually propelled through a carefully shaped mechanism, like an automated slot machine dispensing, say, toys or bottles, rather than a simple hole through which a substance might 'flow'. The goods-dispenser itself is made of a rather small number of protein molecules, each one comparable in size and complexity to the molecules being dispensed through it. Interestingly, these bacterial slot machines are often similar across bacteria that are not closely related. The genes for making them have probably been 'copied and pasted' from other bacteria: something that bacteria are remarkably adept at doing, and a fascinating topic in its own right, but I must press on.

  The protein molecules that form the structure of the TTSS are very similar to components of the flagellar motor. To the evolutionist it is clear that TTSS components were commandeered for a new, but not wholly unrelated, function when the flagellar motor evolved. Given that the TTSS is tugging molecules through itself, it is not surprising that it uses a rudimentary version of the principle used by the flagellar motor, which tugs the molecules of the axle round and round. Evidently, crucial components of the flagellar motor were already in place and working before the flagellar motor evolved. Commandeering existing mechanisms is an obvious way in which an apparently irreducibly complex piece of apparatus could climb Mount Improbable.