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April 21 - June 12, 2023
Eyes don’t fossilize, so we don’t know how long our type of eye took to evolve its present complexity and perfection from nothing, but the time available is several hundred million years.
Mutation is random; natural selection is the very opposite of random.
We have seen that living things are too improbable and too beautifully ‘designed’ to have come into existence by chance. How, then, did they come into existence? The answer, Darwin’s answer, is by gradual, step-by-step transformations from simple beginnings, from primordial entities sufficiently simple to have come into existence by chance.
The kind of non-randomness that can be generated by simple sieving is roughly equivalent to opening a combination lock with only one dial: it is easy to open it by sheer luck. The kind of non-randomness that we see in living systems, on the other hand, is equivalent to a gigantic combination lock with an almost uncountable number of dials.
Chance is a minor ingredient in the Darwinian recipe, but the most important ingredient is cumulative selection which is quintessentially nonrandom.
Evolution has no long-term goal. There is no long-distance target, no final perfection to serve as a criterion for selection, although human vanity cherishes the absurd notion that our species is the final goal of evolution. In real life, the criterion for selection is always short-term, either simple survival or, more generally, reproductive success.
The human eye is here doing exactly what it does in the breeding of pedigree dogs or prize roses. Our model, in other words, is strictly a model of artificial selection, not natural selection. The criterion for ‘success’ is not the direct criterion of survival, as it is in true natural selection.
But natural selection doesn’t choose genes directly, it chooses the effects that genes have on bodies, technically called phenotypic effects.
The actual animals that have ever lived on Earth are a tiny subset of the theoretical animals that could exist. These real animals are the products of a very small number of evolutionary trajectories through genetic space. The vast majority of theoretical trajectories through animal space give rise to impossible monsters.
How can we resolve this apparent contradiction? One kind of answer suggests that bird vision has been improving over the same evolutionary timespan as insect camouflage.
Another kind of answer that has been offered to the dilemma is the following. Perhaps each species of bird or monkey has poor vision and latches onto just one limited aspect of an insect. Maybe one predator species notices only the colour, another only the shape, another only the texture, and so on. Then an insect that resembles a stick in only one limited respect will fool one kind of predator, even though it is eaten by all other kinds of predators. As evolution progresses, more and more features of resemblance are added to the repertoire of the insects. The final multifaceted perfection of
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The swimming mollusc Nautilus, a rather strange squid-like creature that lives in a shell like the extinct ammonites (see the ‘shelled cephalopod’ of Figure 5), has a pair of pinhole cameras for eyes.
The Neck of the Giraffe goes on to discuss the bombardier beetle, which squirts a lethal mixture of hydroquinone and hydrogen peroxide into the face of its enemy. These two chemicals, when mixed together, literally explode. So in order to store them inside its body, the Bombardier Beetle has evolved a chemical inhibitor to make them harmless. At the moment the beetle squirts the liquid out of its tail, an antiinhibitor is added to make the mixture explosive once again. The chain of events that could have led to the evolution of such a complex, coordinated and subtle process is beyond
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The statement that ‘these two chemicals, when mixed together, literally explode’, is, quite simply, false, although it is regularly repeated throughout creationist literature.
It is true that it squirts a scaldingly hot mixture of hydrogen peroxide and hydroquinone at enemies. But hydrogen peroxide and hydroquinone don’t react violently together unless a catalyst is added. This is what the bombardier beetle does.
Indian climbing perch,
Darwin wrote (in The Origin of Species): 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.
The skates and rays, relatives of sharks, have become flat in what might be called the obvious way. Their bodies have grown out sideways to form great ‘wings’. They are like sharks that have passed under a steam roller, but they remain symmetrical and ‘the right way up’.
The whole skull of a bony flatfish retains the twisted and distorted evidence of its origins. Its very imperfection is powerful testimony of its ancient history, a history of step-by-step change rather than of deliberate design. No sensible designer would have conceived such a monstrosity if given a free hand to create a flatfish on a clean drawing board.
The basic rationale is that, if a design is good enough to evolve once, the same design principle is good enough to evolve twice, from different starting points, in different parts of the animal kingdom.
The birds that do it are the oil-birds of South America, and the cave swiftlets of the Far East, the ones whose nests are used for birds’ nest soup.
The intriguing suggestion has been made that dolphins, if they chose to use it, have a potentially effortless means of communicating ‘mental pictures’ to one another.
And if these plagues are carefully timed to occur a prime number of years apart, it makes it that much more difficult for the enemies to synchronize their own life cycles. If the cicadas erupted every 14 years, for instance, they could be exploited by a parasite species with a 7-year life cycle. This is a bizarre idea, but no more bizarre than the phenomenon itself. We really don’t know what is special about 13 and 17 years. What matters for our purposes here is that there must be something special about those numbers, because three different species of cicada have independently converged upon
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The theory that continents drifted about was proposed long ago by the German geophysicist Alfred Wegener, but most people laughed at him until well after the Second World War. The admitted fact that South America and Africa look a bit like separated pieces of a jigsaw puzzle was assumed to be just an amusing coincidence.
Up until about 100 million years ago, then, South America was joined to Africa in the east and to Antarctica in the south. Antarctica was joined to Australia, and India was joined to Africa via Madagascar. There was in fact one huge southern continent, which we now call Gondwanaland, consisting of what is now South America, Africa, Madagascar, India, Antarctica and Australia all rolled into one. There was also a single large northern continent called Laurasia consisting of what is now North America, Greenland, Europe and Asia (apart from India). North America was not connected to South
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An important trade is concerned with the exploitation of the great grasslands variously known as prairie, pampas, savannah, etc. Practitioners of this trade include horses (of which the main African species are called zebras and the desert models are called donkeys), and cattle, such as the North American bison, now hunted to near-extinction.
Each one of these big herbivores is a mountain of valuable food to any predator that can exploit it. As a consequence of this there is, as we shall see, a whole trade devoted to the difficult task of catching and killing them. These are the predators.
There were massive rhino-like Leviathans that had no connection with true rhinos. The skulls of some of the early South American herbivores suggest that they ‘invented’ the trunk independently of the true elephants. Some resembled camels, some looked like nothing on earth (today), or like weird chimeras of modern animals. The group called the litopterns are almost unbelievably similar to horses in their legs, yet they were utterly unrelated to horses.
It is not to be confused with the dingo, by the way, which is a true dog, introduced to Australia more recently by (aboriginal) man. A ciné film made in the 1930s of the last known thylacine, restlessly pacing its lonely zoo cage, shows an uncannily dog-like animal, its marsupial nature betrayed only by its slightly undog-like way of holding its pelvis and back legs, presumably something to do with accommodating its pouch.
Thylacosmilus,
Myrmecophaga
Myrmecobius,
aardvark,
It is worth getting this formidable reputation into perspective by quoting the words of Edward O. Wilson, the world’s foremost authority on ants as well as the author of Sociobiology: In answer to the single question I am asked most frequently about ants, I can give the following answer: No, driver ants are not really the terror of the jungle. Although the driver ant colony is an ‘animal’ weighing in excess of 20 kg and possessing on the order of 20 million mouths and stings and is surely the most formidable creation of the insect world, it still does not match up to the lurid stories told
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My soldiers had inherited the same genes from the present queen as those old soldiers had inherited from the ancestral queens. My soldiers were guarding the master copies of the very instructions that made them do the guarding. They were guarding the wisdom of their ancestors, the Ark of the Covenant. These strange statements will be made plain in the next chapter.
What is special is that these molecules are put together in much more complicated patterns than the molecules of nonliving things, and this putting together is done by following programs, sets of instructions for how to develop, which the organisms carry around inside themselves.
If you want a metaphor, don’t think of fires and sparks and breath. Think, instead, of a billion discrete, digital characters carved in tablets of crystal.
The information technology of the genes is digital. This fact was discovered by Gregor Mendel in the last century, although he wouldn’t have put it like that. Mendel showed that we don’t blend our inheritance from our two parents. We receive our inheritance in discrete particles.
In Darwin’s time everybody (except Mendel who, tucked away in his monastery, was unfortunately ignored until after his death) thought that inheritance was blending.
There is very little difference, in principle, between a two-state binary information technology like ours, and a four-state information technology like that of the living cell.
every location along the chromosome is precisely addressed in terms of linear order along the length of the chromosome, just as every location along a computer tape is precisely addressed, even if the tape is strewn around the floor rather than being neatly rolled up.
There are 20 kinds of amino acids in living cells. All biological proteins are chains made of these 20 basic building-blocks.
There is a fundamental distinction between these two routes of transmission of the DNA information, vertical and horizontal transmission. The information is transmitted vertically to other DNA in cells (that make other cells) that make sperms or eggs. Hence it is transmitted vertically to the next generation and then, vertically again, to an indefinite number of future generations. I shall call this ‘archival DNA’.
It is potentially immortal. The succession of cells along which archival DNA travels is called the germ line. The germ line is that set of cells, within a body, which is ancestral to sperms or eggs and hence ancestral to future generations.
DNA is also transmitted sideways or horizontally: to DNA in non-germ-line cells such as liver cells or skin cells; within such cells to RNA, thence to protein and various effects on embryonic d...
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