The God Delusion

by Richard Dawkins

  A lot more work needs to be done, of course, and I'm sure it will be. Such work would never be done if scientists were satisfied with a lazy default such as 'intelligent design theory' would encourage. Here is the message that an imaginary 'intelligent design theorist' might broadcast to scientists: 'If you don't understand how something works, never mind: just give up and say God did it. You don't know how the nerve impulse works? Good! You don't understand how memories are laid down in the brain? Excellent! Is photosynthesis a bafflingly complex process? Wonderful! Please don't go to work on the problem, just give up, and appeal to God. Dear scientist, don't work on your mysteries. Bring us your mysteries, for we can use them. Don't squander precious ignorance by researching it away. We need those glorious gaps as a last refuge for God.' St Augustine said it quite openly: 'There is another form of temptation, even more fraught with danger. This is the disease of curiosity. It is this which drives us to try and discover the secrets of nature, those secrets which are beyond our understanding, which can avail us nothing and which man should not wish to learn' (quoted in Freeman 2002).

  Another of Behe's favourite alleged examples of 'irreducible complexity' is the immune system. Let Judge Jones himself take up the story:

  In fact, on cross-examination, Professor Behe was questioned concerning his 1996 claim that science would never find an evolutionary explanation for the immune system. He was presented with fifty-eight peer-reviewed publications, nine books, and several immunology textbook chapters about the evolution of the immune system; however, he simply insisted that this was still not sufficient evidence of evolution, and that it was not 'good enough.'

  Behe, under cross-examination by Eric Rothschild, chief counsel for the plaintiffs, was forced to admit that he hadn't read most of those fifty-eight peer-reviewed papers. Hardly surprising, for immunology is hard work. Less forgivable is that Behe dismissed such research as 'unfruitful'. It certainly is unfruitful if your aim is to make propaganda among gullible laypeople and politicians, rather than to discover important truths about the real world. After listening to Behe, Rothschild eloquently summed up what every honest person in that courtroom must have felt:

  Thankfully, there are scientists who do search for answers to the question of the origin of the immune system . . . It's our defense against debilitating and fatal diseases. The scientists who wrote those books and articles toil in obscurity, without book royalties or speaking engagements. Their efforts help us combat and cure serious medical conditions. By contrast, Professor Behe and the entire intelligent design movement are doing nothing to advance scientific or medical knowledge and are telling future generations of scientists, don't bother.64

  As the American geneticist Jerry Coyne put it in his review of Behe's book: 'If the history of science shows us anything, it is that we get nowhere by labelling our ignorance "God".' Or, in the words of an eloquent blogger, commenting on an article on intelligent design in the Guardian by Coyne and me,

  Why is God considered an explanation for anything? It's not - it's a failure to explain, a shrug of the shoulders, an 'I dunno' dressed up in spirituality and ritual. If someone credits something to God, generally what it means is that they haven't a clue, so they're attributing it to an unreachable, unknowable sky-fairy. Ask for an explanation of where that bloke came from, and odds are you'll get a vague, pseudo-philosophical reply about having always existed, or being outside nature. Which, of course, explains nothing.65

  Darwinism raises our consciousness in other ways. Evolved organs, elegant and efficient as they often are, also demonstrate revealing flaws - exactly as you'd expect if they have an evolutionary history, and exactly as you would not expect if they were designed. I have discussed examples in other books: the recurrent laryngeal nerve, for one, which betrays its evolutionary history in a massive and wasteful detour on its way to its destination. Many of our human ailments, from lower back pain to hernias, prolapsed uteruses and our susceptibility to sinus infections, result directly from the fact that we now walk upright with a body that was shaped over hundreds of millions of years to walk on all fours. Our consciousness is also raised by the cruelty and wastefulness of natural selection. Predators seem beautifully 'designed' to catch prey animals, while the prey animals seem equally beautifully 'designed' to escape them. Whose side is God on?66

  THE ANTHROPIC PRINCIPLE: PLANETARY VERSION

  Gap theologians who may have given up on eyes and wings, flagellar motors and immune systems, often pin their remaining hopes on the origin of life. The root of evolution in non-biological chemistry somehow seems to present a bigger gap than any particular transition during subsequent evolution. And in one sense it is a bigger gap. That one sense is quite specific, and it offers no comfort to the religious apologist. The origin of life only had to happen once. We therefore can allow it to have been an extremely improbable event, many orders of magnitude more improbable than most people realize, as I shall show. Subsequent evolutionary steps are duplicated, in more or less similar ways, throughout millions and millions of species independently, and continually and repeatedly throughout geological time. Therefore, to explain the evolution of complex life, we cannot resort to the same kind of statistical reasoning as we are able to apply to the origin of life. The events that constitute run-of-the-mill evolution, as distinct from its singular origin (and perhaps a few special cases), cannot have been very improbable.

  This distinction may seem puzzling, and I must explain it further, using the so-called anthropic principle. The anthropic principle was named by the British mathematician Brandon Carter in 1974 and expanded by the physicists John Barrow and Frank Tipler in their book on the subject.67 The anthropic argument is usually applied to the cosmos, and I'll come to that. But I'll introduce the idea on a smaller, planetary scale. We exist here on Earth. Therefore Earth must be the kind of planet that is capable of generating and supporting us, however unusual, even unique, that kind of planet might be. For example, our kind of life cannot survive without liquid water. Indeed, exobiologists searching for evidence of extraterrestrial life are scanning the heavens, in practice, for signs of water. Around a typical star like our sun, there is a so-called Goldilocks zone - not too hot and not too cold, but just right - for planets with liquid water. A thin band of orbits lies between those that are too far from the star, where water freezes, and too close, where it boils.

  Presumably, too, a life-friendly orbit has to be nearly circular. A fiercely elliptical orbit, like that of the newly discovered tenth planet informally known as Xena, would at best allow the planet to whizz briefly through the Goldilocks zone once every few (Earth) decades or centuries. Xena itself doesn't get into the Goldilocks zone at all, even at its closest approach to the sun, which it reaches once every 560 Earth years. The temperature of Halley's Comet varies between about 47°C at perihelion and minus 270°C at aphelion. Earth's orbit, like those of all the planets, is technically an ellipse (it is closest to the sun in January and furthest away in July*); but a circle is a special case of an ellipse, and Earth's orbit is so close to circular that it never strays out of the Goldilocks zone. Earth's situation in the solar system is propitious in other ways that singled it out for the evolution of life. The massive gravitational vacuum cleaner of Jupiter is well placed to intercept asteroids that might otherwise threaten us with lethal collision. Earth's single relatively large moon serves to stabilize our axis of rotation,68 and helps to foster life in various other ways. Our sun is unusual in not being a binary, locked in mutual orbit with a companion star. It is possible for binary stars to have planets, but their orbits are likely to be too chaotically variable to encourage the evolution of life.

  * If you find that surprising, you may be suffering from northern hemisphere chauvinism, as described on page 114-15.

  Two main explanations have been offered for our planet's peculiar friendliness to life. The design theory says that God made the world, placed it in the Goldilocks zone, and deliberately set up all the details for our benefit.
The anthropic approach is very different, and it has a faintly Darwinian feel. The great majority of planets in the universe are not in the Goldilocks zones of their respective stars, and not suitable for life. None of that majority has life. However small the minority of planets with just the right conditions for life may be, we necessarily have to be on one of that minority, because here we are thinking about it.

  It is a strange fact, incidentally, that religious apologists love the anthropic principle. For some reason that makes no sense at all, they think it supports their case. Precisely the opposite is true. The anthropic principle, like natural selection, is an alternative to the design hypothesis. It provides a rational, design-free explanation for the fact that we find ourselves in a situation propitious to our existence. I think the confusion arises in the religious mind because the anthropic principle is only ever mentioned in the context of the problem that it solves, namely the fact that we live in a life-friendly place. What the religious mind then fails to grasp is that two candidate solutions are offered to the problem. God is one. The anthropic principle is the other. They are alternatives.

  Liquid water is a necessary condition for life as we know it, but it is far from sufficient. Life still has to originate in the water, and the origin of life may have been a highly improbable occurrence. Darwinian evolution proceeds merrily once life has originated. But how does life get started? The origin of life was the chemical event, or series of events, whereby the vital conditions for natural selection first came about. The major ingredient was heredity, either DNA or (more probably) something that copies like DNA but less accurately, perhaps the related molecule RNA. Once the vital ingredient - some kind of genetic molecule - is in place, true Darwinian natural selection can follow, and complex life emerges as the eventual consequence. But the spontaneous arising by chance of the first hereditary molecule strikes many as improbable. Maybe it is - very very improbable, and I shall dwell on this, for it is central to this section of the book.

  The origin of life is a flourishing, if speculative, subject for research. The expertise required for it is chemistry and it is not mine. I watch from the sidelines with engaged curiosity, and I shall not be surprised if, within the next few years, chemists report that they have successfully midwifed a new origin of life in the laboratory. Nevertheless it hasn't happened yet, and it is still possible to maintain that the probability of its happening is, and always was, exceedingly low - although it did happen once!

  Just as we did with the Goldilocks orbits, we can make the point that, however improbable the origin of life might be, we know it happened on Earth because we are here. Again as with temperature, there are two hypotheses to explain what happened - the design hypothesis and the scientific or 'anthropic' hypothesis. The design approach postulates a God who wrought a deliberate miracle, struck the prebiotic soup with divine fire and launched DNA, or something equivalent, on its momentous career.

  Again, as with Goldilocks, the anthropic alternative to the design hypothesis is statistical. Scientists invoke the magic of large numbers. It has been estimated that there are between 1 billion and 30 billion planets in our galaxy, and about 100 billion galaxies in the universe. Knocking a few noughts off for reasons of ordinary prudence, a billion billion is a conservative estimate of the number of available planets in the universe. Now, suppose the origin of life, the spontaneous arising of something equivalent to DNA, really was a quite staggeringly improbable event. Suppose it was so improbable as to occur on only one in a billion planets. A grant-giving body would laugh at any chemist who admitted that the chance of his proposed research succeeding was only one in a hundred. But here we are talking about odds of one in a billion. And yet . . . even with such absurdly long odds, life will still have arisen on a billion planets - of which Earth, of course, is one.69

  This conclusion is so surprising, I'll say it again. If the odds of life originating spontaneously on a planet were a billion to one against, nevertheless that stupefyingly improbable event would still happen on a billion planets. The chance of finding any one of those billion life-bearing planets recalls the proverbial needle in a haystack. But we don't have to go out of our way to find a needle because (back to the anthropic principle) any beings capable of looking must necessarily be sitting on one of those prodigiously rare needles before they even start the search.

  Any probability statement is made in the context of a certain level of ignorance. If we know nothing about a planet, we may postulate the odds of life's arising on it as, say, one in a billion. But if we now import some new assumptions into our estimate, things change. A particular planet may have some peculiar properties, perhaps a special profile of element abundances in its rocks, which shift the odds in favour of life's emerging. Some planets, in other words, are more 'Earth-like' than others. Earth itself, of course, is especially Earth-like! This should give encouragement to our chemists trying to recreate the event in the lab, for it could shorten the odds against their success. But my earlier calculation demonstrated that even a chemical model with odds of success as low as one in a billion would still predict that life would arise on a billion planets in the universe. And the beauty of the anthropic principle is that it tells us, against all intuition, that a chemical model need only predict that life will arise on one planet in a billion billion to give us a good and entirely satisfying explanation for the presence of life here. I do not for a moment believe the origin of life was anywhere near so improbable in practice. I think it is definitely worth spending money on trying to duplicate the event in the lab and - by the same token, on SETI, because I think it is likely that there is intelligent life elsewhere.

  Even accepting the most pessimistic estimate of the probability that life might spontaneously originate, this statistical argument completely demolishes any suggestion that we should postulate design to fill the gap. Of all the apparent gaps in the evolutionary story, the origin of life gap can seem unbridgeable to brains calibrated to assess likelihood and risk on an everyday scale: the scale on which grant-giving bodies assess research proposals submitted by chemists. Yet even so big a gap as this is easily filled by statistically informed science, while the very same statistical science rules out a divine creator on the 'Ultimate 747' grounds we met earlier.

  But now, to return to the interesting point that launched this section. Suppose somebody tried to explain the general phenomenon of biological adaptation along the same lines as we have just applied to the origin of life: appealing to an immense number of available planets. The observed fact is that every species, and every organ that has ever been looked at within every species, is good at what it does. The wings of birds, bees and bats are good at flying. Eyes are good at seeing. Leaves are good at photo-synthesizing. We live on a planet where we are surrounded by perhaps ten million species, each one of which independently displays a powerful illusion of apparent design. Each species is well fitted to its particular way of life. Could we get away with the 'huge numbers of planets' argument to explain all these separate illusions of design? No, we could not, repeat not. Don't even think about it. This is important, for it goes to the heart of the most serious misunderstanding of Darwinism.

  It doesn't matter how many planets we have to play with, lucky chance could never be enough to explain the lush diversity of living complexity on Earth in the same way as we used it to explain the existence of life here in the first place. The evolution of life is a completely different case from the origin of life because, to repeat, the origin of life was (or could have been) a unique event which had to happen only once. The adaptive fit of species to their separate environments, on the other hand, is millionfold, and ongoing.

  It is clear that here on Earth we are dealing with a generalized process for optimizing biological species, a process that works all over the planet, on all continents and islands, and at all times. We can safely predict that, if we wait another ten million years, a whole new set of species will be as well adapted to their ways of life as today's species are
to theirs. This is a recurrent, predictable, multiple phenomenon, not a piece of statistical luck recognized with hindsight. And, thanks to Darwin, we know how it is brought about: by natural selection.

  The anthropic principle is impotent to explain the multifarious details of living creatures. We really need Darwin's powerful crane to account for the diversity of life on Earth, and especially the persuasive illusion of design. The origin of life, by contrast, lies outside the reach of that crane, because natural selection cannot proceed without it. Here the anthropic principle comes into its own. We can deal with the unique origin of life by postulating a very large number of planetary opportunities. Once that initial stroke of luck has been granted - and the anthropic principle most decisively grants it to us - natural selection takes over: and natural selection is emphatically not a matter of luck.

  Nevertheless, it may be that the origin of life is not the only major gap in the evolutionary story that is bridged by sheer luck, anthropically justified. For example, my colleague Mark Ridley in Mendel's Demon (gratuitously and confusingly retitled The Cooperative Gene by his American publishers) has suggested that the origin of the eucaryotic cell (our kind of cell, with a nucleus and various other complicated features such as mitochondria, which are not present in bacteria) was an even more momentous, difficult and statistically improbable step than the origin of life. The origin of consciousness might be another major gap whose bridging was of the same order of improbability. One-off events like this might be explained by the anthropic principle, along the following lines. There are billions of planets that have developed life at the level of bacteria, but only a fraction of these life forms ever made it across the gap to something like the eucaryotic cell. And of these, a yet smaller fraction managed to cross the later Rubicon to consciousness. If both of these are one-off events, we are not dealing with a ubiquitous and all-pervading process, as we are with ordinary, run-of-the-mill biological adaptation. The anthropic principle states that, since we are alive, eucaryotic and conscious, our planet has to be one of the intensely rare planets that has bridged all three gaps.