The Big Picture

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The Big Picture Page 47

by Carroll, Sean M.


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  would be hard to create a new universe.

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  But it’s not impossible. (At least for evolution; we still don’t know how

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  to create new universes.) And that’s exactly what Lenski set out to do.

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  His basic setup was— and is, as the experiment is still ongoing— a sim-

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  ple one. He started with twelve flasks containing growth medium: a liquid

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  with a specific mixture of chemicals, including a bit of glucose to provide

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  energy. He then introduced a population of identical E. coli bacteria into

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  each of them. Every day, each flask goes from a few million to a few hun-

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  dred million cells. One percent of the surviving bacteria are extracted and

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  moved to new flasks with the same growth medium as before. The remain-

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  ing bacteria are mostly disposed of, although every so often a sample is fro-

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  zen for future examination, creating an experimental “fossil record.”

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  (Unlike human beings, live bacteria can easily be frozen and revived at a

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  later date using current technology.) The total population growth amounts

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  to about six and a half generations in a day; the limiting resource is nutri-

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  tion, not time (it takes less than an hour for a cell to divide). As of late 2015,

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  this added up to more than 60,000 generations of bacteria— enough for

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  some interesting evolutionary wrinkles to develop.

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  Confined to this extremely specific and stable environment, the evolved

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  bacteria are by now quite well adapted to their surroundings. They are now

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  over twice the size of the individuals in the original population, and they

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  reproduce more rapidly than before. They have become very good at me-

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  tabolizing glucose, while generally decaying in their ability to thrive in

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  more diverse nutrient environments.

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  Most impressively, there have been qualitative as well as quantitative

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  changes in the E. coli. Among the ingredients in the initial growth medium

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  was citrate, an acid made of carbon, hydrogen, and oxygen. The original

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  bacteria had no ability to use this compound. But around generation

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  31,000, Lenski and his collaborators noticed that the population in one

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  particular flask had grown larger than the others. Looking more closely,

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  they realized that some of the bacteria in that flask had developed the abil-

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  ity to metabolize citrate, rather than just glucose.

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  Citrate is not as good an energy source as glucose is. But if you’re a bac-

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  terium in a flask full of other bacteria that are competing for a fixed amount

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  of glucose, the ability to live off of this other energy source is very useful.

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  Without having any particular goal to work toward, without the benefit of

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  any external prompting or instruction, evolution had come up with a clever

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  new way of allowing organisms to flourish in their particular environment.

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  The origin of life was the mother of all phase transitions. Like other chem-

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  ical reactions or combinations thereof, life proceeds by converting free en-

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  ergy into disordered energy. The aspect that makes life special among

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  chemical reactions is that it carries with it a set of instructions. Like the

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  tape in one of John von Neumann’s Universal Constructors, the genetic

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  information contained in DNA regulates and guides the interconnected

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  dance of reactions that defines a living organism. Those instructions can

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  change as they are passed down from generation to generation. That ability

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  is what gets natural selection off the ground.

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  We’ve speculated that DNA came from RNA, which in turn may have

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  self- catalyzed its own production under the right circumstances. It’s possi-

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  ble that the creation of the first RNA molecule involved random fluctua-

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  tions at critical points along the way. Boltzmann taught us that entropy

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  usual y increases, but there is always some probability that it will occasion-

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  ally move downward. The more moving parts a system has, the more rare

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  such fluctuations will be; at macroscopic scales, the number of atoms in-

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  volved is so large that it’s not worth worrying about. But at the level of in-

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  dividual molecules, rare fluctuations are frequent enough to be important.

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  The appearance of the first self- replicating RNA molecule might just have

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  been a matter of good luck.

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  We sometimes think of natural selection as “survival of the fittest.” But

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  even before evolution in Darwin’s sense officially kicked in, there was a

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  competition of sorts going on for the available free energy. Some of it would

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  have been readily accessible, but some— similarly to that locked up in the

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  citrate in Richard Lenski’s flasks of bacteria— would have required more

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  ingenuity to unlock. An intricate network of reactions, directed by proteins

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  created by a sequence of nucleotides in RNA, could have prospered where

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  simpler processes would have flickered out. Once heritable genetic informa-

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  tion starts playing a role, all of the ingredients are in place for natural selec-

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  tion to commence.

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  From a certain perspective, Darwin’s theory is sufficiently commonsensical

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  that it seems almost inevitable. Upon first reading Origin, Thomas Henry 25

  Huxley, Darwin’s contemporary and vocal supporter, exclaimed, “How ex-

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  tremely stupid not to have thought of that!” But natural selection is a very

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  specific process, and by no means inevitable or obvious. It’s not simply “spe-

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  cies gradually change over time,” or “ well- adapted organisms are more likely

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  to reproduce.”

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  Organisms reproduce, and they hand down their genetic information to

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  the next generation. That information is largely stable— children resemble

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  their parents— but it’s not absolutely fixed. Small, random variations can be

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  introduced at every step. The variations do not strive to reach any future

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  goals, and neither can individual organisms influence them by their actions.

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  (Your offspring don’t become more muscular just because you work out.) If

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  we have descent with inheritance, and there is slight, random variation in

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  the genetic information that can affect the likelihood of reproduction,

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  natural selection can occur. Variations that fortuitously improve an organ-

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  ism’s chances of handing down its genetic heritage will be more likely to

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  persist than those that are harmful or neutral.

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  These ingredients shouldn’t be taken for granted. This is why biologists

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  highlight the difference between “evolution” and “natural selection.” The

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  former is the change of the genome (complete set of genetic information)

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  over time; the latter refers to the specific case where changes in the genome

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  are driven by different amounts of reproductive success.

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  Darwin didn’t know about DNA or RNA, or even of genes, discrete

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  units of inherited information. It was the Augustinian monk Gregor Men-

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  del who established the basic rules of heredity, through a set of now- famous

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  experiments crossing different varieties of pea plants. In the 1930s and ’40s,

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  biologists developed the modern synthesis, combining natural selection with

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  Mendelian genetics. The paradigm continues to be elaborated upon as we

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  learn more and more about biology and inheritance, but the basic picture

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  remains enormously successful.

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  The reality of biology here on Earth is, unsurprisingly, more compli-

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  cated than the simplest statement of natural selection. Like any way of talk-

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  ing about the world, Darwin’s theory works only within its domain of

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  applicability.

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  There are forces at work in the history of life other than organisms

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  adapting to their environments. This is completely compatible with Dar-

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  win’s conception; natural selection happens, but it happens within the

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  messiness of the real world, and it’s not the only thing happening. Many

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  features of the genome of any individual species are going to be the results

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  of accidents rather than any particular adaptation. This is known as genetic

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  drift. Sometimes there will be mutations that neither increase nor decrease

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  the fitness of an organism; other times, the randomness inherent in sexual

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  reproduction or unpredictable features of the environment will cause some

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  traits to become common while others die off. Biologists debate the relative

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  importance of adaptation and genetic drift, but there is little doubt that

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  both are important.

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  In Lenski’s long- term evolution experiment, the mutation that allowed

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  some of the bacteria to metabolize citrate occurred around generation

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  31,000. When the researchers unfroze some of the earlier generations to see

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  if they would evolve this ability again, they found that the answer was yes—

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  but only when they started with cells from generation 20,000 or later.

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  Around generation 20,000, one or more mutations must have occurred that

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  did not themselves allow the bacteria to metabolize citrate, but set the stage

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  for a later mutation that would do so. A single trait can be brought to life

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  by multiple, separate mutations, which may not individually have much

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  noticeable impact at all.

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  Selection pressures work on traits, while genetic information is passed

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  down through DNA, and the map from one to the other isn’t a simple one.

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  Something as basic as how tall a person is won’t typically be fixed by one

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  particular string of nucleotides, but instead will depend on an interplay

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  between different factors working simultaneously. As a result, selection

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  pressure acting on one trait may end up affecting another one, if they de-

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  pend on common sets of DNA sequences. Evolutionary history is replete

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  with “spandrels,” as was famously emphasized by biologists Stephen Jay

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  Gould and Richard Lewontin. These are traits that arise for one reason and

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  then end up being used for something quite different. By-products of the

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  evolutionary process, rather than aspects that are directly selected for.

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  Gould and Lewontin imagine that many features of the human brain fall

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  under this category.

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  To make matters worse, inheritance can be more than simply a matter

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  of passing down DNA from one generation to the next. There is horizontal

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  gene transfer, in which genes are passed from one organism to another in a

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  way other than reproduction. It is relatively common in bacteria, and oc-

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  casionally happens in multicellular species. There are epigenetic phenomena,

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  in which the chemical structure of inherited DNA is modified during de-

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  velopment by influences such as the nutritional intake of an organism and

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  the maternal environment in which an embryo develops. It is currently

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  unclear how much such changes can be inherited by subsequent genera-

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  tions, but to the extent that they are, natural selection will act upon them

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  as usual.

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  So the real world is a beautiful mess. Is this kind of undirected

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  mechanism— just what we would expect in a universe governed by un-

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  thinking underlying laws and with a strong arrow of time— sufficient to

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  account for all the spectacular intricacy of our planet’s biosphere? “There is

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  grandeur in this view of life,” Darwin writes in On the Origin of Species. But 02

  is his simple mechanism really enough to make dolphins and butterflies and

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  rain forests from a meager collection of organic molecules fighting for free

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  energy? Can the wonders of efficiency and ingenuity we see in biological

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  organisms really come about from random variation plus time? (Hint: yes.)

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  Searching through the Landscape

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  I

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  n computer science, as in life, we are often faced with the simple prob-

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  lem of finding some particular item in a long list of possibilities. Con-

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  sider the traveling- salesman problem: given a list of cities and the

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  distances between them, what is the shortest route that visits each city ex-

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  actly once? That can be rephrased in the following way. Take a list of cities

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  and the distances between them. Now make another list, consisting of ev-

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  ery possible route that goes through each city at least once. (It will be an

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  enormously longer list, but it is still finite.) Which route is the shortest?

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  A search algorithm is a precisely stated procedure for finding what you

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  are looking for in a list of objects. Of course you could trudge through every

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  element of the list, asking, “Is this the one?” That can be hard, since quite

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  reasonable- sounding questions can involve very unreasonably sized lists to

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  sort through. For the traveling- salesman problem, the number of possible

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  routes grows roughly as the factorial of the number of cities involved. The

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  factorial of a number n is equal to 1 times 2 times 3 times 4 . . . times ( n – 1) 28

  times n. For twenty- seven cities, that’s about 1028 routes to search through.

 

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