Tag: David Quammen

Immigration, Extinction, and Island Equilibrium

Reading Time: 4 minutes

Equilibrium is an important concept that permeates many disciplines. In chemistry we think about the point where the rate of forward reaction is equal to the rate of backward reaction. In economics we think of the point where supply equals demand. In physics we can see how gravity is balanced by forward velocity to create things like planetary orbits.

No matter which discipline we are examining, the core idea remains the same: Equilibrium is a state where opposing forces are balanced.

In biology, equilibrium is so important that it can mean the difference between life or death; for a species, it can decide whether they will thrive or become extinct.

In The Song of the Dodo, David Quammen dives into how equilibrium affects a species’ ability to survive, and how it impacts our ability to save animals on the brink of extinction.

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Historically, the concept of island equilibrium was studied with a focus on the interplay between evolution (as the additive) and extinction (as the subtractive). It was believed that speciation, the process where one species becomes two or more species, caused any increase in the number of inhabitants on an island. In this view, the insularity of islands created a remoteness that could only be overcome by the long processes of evolution. 

However, Robert MacArthur and E.O. Wilson, the co-authors of the influential Theory of Island Biogeography, realized that habitats would show a tendency towards equilibrium much sooner than could be accounted for by speciation. They argued the ongoing processes that most influenced this balance were immigration and extinction.

The type of extinctions we’re referring to in this case are local extinctions, specific to the island in question. A species can go extinct on a particular island and yet be thriving elsewhere; it depends on local conditions.

As for immigration, it’s just what you’d expect: The movement of species from one place to another. Island immigration describes the many ingenious ways in which plants, animals, and insects travel to islands. For instance, not only will insects hitch rides on birds and debris (man made or natural, think garbage and sticks/uprooted seaweed), animals will do the same if the debris is massive enough.

Seeds, meanwhile, make the trip in the feces of birds, which helps to introduce new plant species to the island, while highly motivated swimmers (escapees of natural disasters/predators/famine) and hitchhikers on human ships (think rats) make it over in their own unusual ways.

We can plot this process of immigration and extinction graphically, in a way you’re probably familiar with. Quammen explains:

picture1

The decrease in immigration rate and the increase in extinction rate are graphed not against elapsed time but against the number of species present on a given island. As an island fills up with species, immigration declines and extinction increases, until they offset each other at an equilibrium level. At that level, the rate of continuing immigration is just canceled by the rate of continuing extinction, and there is no net gain or loss of species. The phenomenon of offsetting increase and decrease – the change of identities on the roster of species – is known as turnover. One species of butterfly arrives, another species of butterfly dies out, and in the aftermath the island has the same number of butterfly species as before. Equilibrium with turnover.

So while the specific species inhabiting the island will change over time, the numbers will tend to roll towards a balanced point where the two curves intersect.

Of course, not all equilibrium graphs will look the like one above. Indeed, MacArthur and Wilson hoped this theory would be used not just to explain equilibriums, but to also help predict potential issues.

When either curve is especially steep – reflecting the fact that immigration decreases especially sharply or extinction increases especially sharply – their crossing point shifts leftward, toward zero. The shift means that, at equilibrium, in this particular set of circumstances, there will be relatively few resident species.

In other words, high extinction and low immigration yield an impoverished ecosystem. To you and me it’s a dot in Cartesian space, but to an island it represents destiny.

There are two key ideas that can help us understand the equilibrium point on a given island.

First, the concept of species-area relationship: We see a larger number of a given species on larger islands and a smaller number of a given species on smaller islands.

Second, the concept of species quantity on remote islands: Immigration is much more difficult the further away an island is from either a mainland or a cluster of other islands, meaning that fewer species will make it there.

In other words, size and remoteness are directly correlated to the fragility of any given species inhabiting an island.

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Equilibrium, immigration, evolution, extinction – these are all ideas that bleed into so many more areas than biogeography. What happens to groups when they are isolated? Jared Diamond had some interesting thoughts on that. What happens to products or businesses which don’t keep up with co-evolution? They go extinct due to the Red Queen Effect. What happens to our mind and body when we feel off balance? Our life is impoverished.

Reading a book like The Song of the Dodo helps us to better understand these key concepts which, in turn, helps us more fundamentally understand the world.

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The Founder Principle: A Wonderful Idea from Biology

Reading Time: 5 minutes

We’ve all been taught natural selection; the mechanism by which species evolve through differential reproductive success. Most of us are familiar with the idea that random mutations in DNA cause variances in offspring, some of which survive more frequently than others. However, this is only part of the story.

Sometimes other situations cause massive changes in species populations, and they’re often more nuanced and tough to spot.

One such concept comes from one of the most influential biologists in history, Ernst Mayr. He called it The Founder Principle, a mechanism by which new species are created by a splintered population; often with lower genetic diversity and an increased risk of extinction.

In the brilliant The Song of the Dodo: Island Biography in an Age of Extinction, David Quammen gives us not only the stories of many brilliant biological naturalists including Mayr, but we also get a deep dive into the core concepts of evolution and extinction, including the founder principle.

Quammen begins by outlining the basic idea:

When a new population is founded in an isolated place, the founders usually constitute a numerically tiny group – a handful of lonely pioneers, or just a pair, or maybe no more than one pregnant female. Descending from such a small number of founders, the new population will carry only a minuscule and to some extent random sample of the gene pool of the base population. The sample will most likely be unrepresentative, encompassing less genetic diversity than the larger pool. This effect shows itself whenever a small sample is taken from a large aggregation of diversity; whether the aggregation consists of genes, colored gum balls, M&M’s, the cards of a deck, or any other collection of varied items, a small sample will usually contain less diversity than the whole.

Why does the founder principle happen? It’s basically applied probability. Perhaps an example will help illuminate the concept.

Think of yourself playing a game of poker (five card draw) with a friend. The deck of cards is separated into four suits: Diamonds, hearts, clubs and spades, each suit having 13 cards for a total of 52 cards.

Now look at your hand of five cards. Do you have one card from each suit? Maybe. Are all five cards from the same suit? Probably not, but it is possible. Will you get the ace of spades? Maybe, but not likely.

This is a good metaphor for how the founder principle works. The gene pool carried by a small group of founders is unlikely to be precisely representative of the gene pool of the larger group. In some rare cases it will be very unrepresentative, like you getting dealt a straight flush.

It starts to get interesting when this founder population starts to reproduce, and genetic drift causes the new population to diverge significantly from its ancestors. Quammen explains:

Already isolated geographically from its base population, the pioneer population now starts drifting away genetically. Over the course of generations, its gene pool becomes more and more different from the gene pool of the base population – different both as to the array of alleles (that is, the variant forms of a given gene) and as to the commonness of each allele.

The founder population, in some cases, will become so different that it can no longer mate with the original population. This new species may even be a competitor for resources if the two populations are ever reintroduced. (Say, if a land bridge is created between two islands, or humans bring two species back in contact.)

Going back to our card metaphor, let’s pretend that you and your friend are playing with four decks of cards — 208 total cards. Say we randomly pulled out forty cards from those decks. If there are absolutely no kings in the forty cards you are playing with, you will never be able to create a royal flush (ace+king+queen+jack+10 of the same suit). It doesn’t matter how the cards are dealt, you can never make a royal flush with no kings.

Thus it is with species: If a splintered-off population isn’t carrying a specific gene variant (allele), that variant can never be represented in the newly created population, no matter how prolific that gene may have been in the original population. It’s gone. And as the rarest variants disappear, the new population becomes increasingly unlike the old one, especially if the new population is small.

Some alleles are common within a population, some are rare. If the population is large, with thousands or millions of parents producing thousands or millions of offspring, the rare alleles as well as the common ones will usually be passed along. Chance operation at high numbers tends to produce stable results, and the proportions of rarity and commonness will hold steady. If the population is small, though, the rare alleles will most likely disappear […] As it loses its rare alleles by the wayside, a small pioneer population will become increasingly unlike the base population from which it derived.

Some of this genetic loss may be positive (a gene that causes a rare disease may be missing), some may be negative (a gene for a useful attribute may be missing) and some may be neutral.

The neutral ones are the most interesting: A neutral gene at one point in time may become a useful gene at another point. It’s like playing a round of poker where 8’s are suddenly declared “wild,” and that card suddenly becomes much more important than it was the hand before. The same goes for animal traits.

Take a mammal population living on an island, having lost all of its ability to swim. That won’t mean much if all is well and it is never required to swim. But the moment there is a natural disaster such as a fire, having the ability to swim the short distance to the mainland could be the difference between survival or extinction.

That’s why the founder principle is so dangerous: The loss of genetic diversity often means losing valuable survival traits. Quammen explains:

Genetic drift compounds the founder-effect problem, stripping a small population of the genetic variation that it needs to continue evolving. Without that variation, the population stiffens toward uniformity. It becomes less capable of adaptive response. There may be no manifest disadvantages in uniformity so long as environmental circumstances remain stable; but when circumstances are disrupted, the population won’t be capable of evolutionary adjustment. If the disruption is drastic, the population may go extinct.

This loss of adaptability is one of the two major issues caused by the founder principle, the second being inbreeding depression. A founder population may have no choice but to only breed within its population and a symptom of too much inbreeding is the manifestation of harmful genetic variants among inbred individuals. (One reason humans consider incest a dangerous activity.) This too increases the fragility of species and decreases their ability to evolve.

The founder principle is just one of many amazing ideas in The Song of the Dodo. In fact, we at Farnam Street feel the book is so important that it made our list of books we recommend to improve your general knowledge of the world and it was the first book we picked for our learning community reading group.

If you have already read this book and want more we suggest Quammen’s The Reluctant Mr. Darwin or his equally thought provoking Spillover: Animal Infections and the Next Human Pandemic. Another wonderful and readable book on species evolution is The Beak of the Finch, by Jonathan Weiner.

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What Can Chain Letters Teach us about Natural Selection?

Reading Time: 6 minutes

“It is important to understand that none of these replicating entities is consciously interested in getting itself duplicated. But it will just happen that the world becomes filled with replicators that are more efficient.”

***

In 1859, Charles Darwin first described his theory of evolution through natural selection in The Origin of Species. Here we are, 157 years later, and although it has become an established fact in the field of biology, its beauty is still not that well understood among the populace. I think that’s because it’s slightly counter-intuitive. Unlike string theory or quantum mechanics, the theory of evolution through natural selection is pretty easily obtainable by most.

So, is there a way we can help ourselves understand the theory in an intuitive way, so we can better go on applying it to other domains? I think so, and it comes from an interesting little volume released in 1995 by the biologist Richard Dawkins called River Out of Eden. But first, let’s briefly head back to the Origin of Species, so we’re clear on what we’re trying to understand.

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In the fourth chapter of the book, entitled “Natural Selection,” Darwin describes a somewhat cold and mechanistic process for the development of species: If species had heritable traits and variation within their population, they would survive in different numbers, and those most adapted to survival would thrive and pass on those traits to successive generations. Eventually, new species would arise, slowly, as enough variation and differential reproduction acted on the population to create a de facto branch in the family tree.

Here’s the original description.

Let it be borne in mind how infinitely complex and close-fitting are the mutual relations of all organic beings to each other and to their physical conditions of life. Can it, then, be thought improbable, seeing that variations useful to man have undoubtedly occurred, that other variations useful in some way to each being in the great and complex battle of life, should sometimes occur in the course of thousands of generations? If such do occur, can we doubt (remembering that many more individuals are born than can possibly survive) that individuals having any advantage, however slight, over others, would have the best chance of surviving and of procreating their kind? On the other hand, we may feel sure that any variation in the least degree injurious would be rigidly destroyed. This preservation of favourable variations and the rejection of injurious variations, I call Natural Selection.

[…]

In such case, every slight modification, which in the course of ages chanced to arise, and which in any way favored the individuals of any species, by better adapting them to their altered conditions, would tend to be preserved; and natural selection would thus have free scope for the work of improvement.

[…]

It may be said that natural selection is daily and hourly scrutinizing, throughout the world, every variation, even the slightest; rejection that which is bad, preserving and adding up all that is good; silently and insensibly working, whenever and wherever opportunity offers, at the improvement of each organic being in relation to its organic and inorganic conditions of life. 

The beauty of the theory is in its simplicity. The mechanism of evolution is, at root, a simple one. An unguided one. Better descendants outperform lesser ones in a competitive world and are more successful at replicating. Traits that improve the survival of their holder in its current environment tend to be preserved and amplified over time. This is hard to see in real time, although some examples are helpful in understanding the concept, e.g. antibiotic resistance.

Darwin’s idea didn’t take as quickly as we might like to think. In The Reluctant Mr. Darwin, David Quammen talks about the period after the release of the groundbreaking work, in which the world had trouble coming to grips with Darwin’s theory. It was not the case, as it might seem today, that the world simply threw up its hands and accepted Darwin as a genius. This is a lesson in and of itself. It was quite the contrary:

By the 1890s, natural selection as Darwin had defined it–that is, differential reproductive success resulting from small, undirected variations and serving as the chief mechanism of adaption and divergence–was considered by many evolutionary biologists to have been a wrong guess.

It wasn’t until Gregor Mendel’s peas showed how heritability worked that Darwin’s ideas were truly vindicated against his rivals’. So if we have trouble coming to terms with evolution by natural selection in the modern age, we’re not alone: So did Darwin’s peers.

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What’s this all got to do with chain letters? Well, in Dawkins’ River Out of Eden, he provides an analogy for the process of evolution through natural selection that is quite intuitive, and helpful in understanding the simple power of the idea. How would a certain type of chain letter come to dominate the population of all chain letters? It would work the same way.

A simple example is the so-called chain letter. You receive in the mail a postcard on which is written: “Make six copies of this card and send them to six friends within a week. If you do not do this, a spell will be cast upon you and you will die in horrible agony within a month.” If you are sensible you will throw it away. But a good percentage of people are not sensible; they are vaguely intrigued, or intimidated by the threat, and send six copies of it to other people. Of these six, perhaps two will be persuaded to send it on to six other people. If, on average, 1/3 of the people who receive the card obey the instructions written on it, the number of cards in circulation will double every week. In theory, this means that the number of cards in circulation after one year will be 2 to the power of 52, or about four thousand trillion. Enough post cards to smother every man, woman, and child in the world.

Exponential growth, if not checked by the lack of resources, always leads to startlingly large-scale results in a surprisingly short time. In practice, resources are limited and other factors, too, serve to limit exponential growth. In our hypothetical example, individuals will probably start to balk when the same chain letter comes around to them for the second time. In the competition for resources, variants of the same replicator may arise that happen to be more efficient at getting themselves duplicated. These more efficient replicators will tend to displace their less efficient rivals. It is important to understand that none of these replicating entities is consciously interested in getting itself duplicated. But it will just happen that the world becomes filled with replicators that are more efficient.

In the case of the chain letter, being efficient may consist in accumulating a better collection of words on the paper. Instead of the somewhat implausible statement that “if you don’t obey the words on the card you will die in horrible agony within a month,” the message might change to “Please, I beg of you, to save your soul and mine, don’t take the risk: if you have the slightest doubt, obey the instructions and send the letter to six more people.”

Such “mutations” happen again and again, and the result will eventually be a heterogenous population of messages all in circulation, all descended from the same original ancestor but differing in detailed wording and in the strength and nature of the blandishments they employ. The variants that are more successful will increase in frequency at the expense of less successful rivals. Success is simply synonymous with frequency in circulation. 

The chain letter contains all of the elements of biological natural selection except one: Someone had to write the first chain letter. The first replicating biological entity, on the other hand, seems to have sprung up from an early chemical brew.

Consider this analogy an intermediate mental “step” towards the final goal. Because we know and appreciate the power of reasoning by analogy and metaphor, we can deduce that finding an appropriate analogy is one of the best ways to pound an idea into your head–assuming it is a correct idea that should be pounded in.

And because evolution through natural selection is one of the more powerful ideas a human being has ever had, it seems worth our time to pound this one in for good and start applying it elsewhere if possible. (For example, Munger has talked about how business evolves in a manner such that competitive results are frequently similar to biological outcomes.)

Read Dawkins’ book in full for a deeper look at his views on replication and natural selection. It’s shorter than some of his other works, but worth the time.

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Evolution and Divergence

Reading Time: 0 minutes Less than a minute

“[A] species of crow and a species of woodpecker can continue to diverge evolutionarily, when while sharing the same forest. They do it by responding differently to different aspects of the environment—that is by adapting themselves to different ecological niches.”

— David Quammen

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David Quammen on Why Big Populations Survive and Small Ones Go Extinct

Reading Time: 4 minutes

“Big populations don’t go extinct. Small populations do.
It’s not a surprising finding but it is a significant one.”
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Why do small populations go extinct?

While the answer is simple to outline the scientific details are more nuanced. For now, lets stick to the outline version.

“Small populations go extinct because (1) all populations fluctuate in size from time to time, under the influence of two kinds of factors, which ecologists refer to as deterministic and stochastic; and (2) small populations, unlike big ones, stand a good chance of fluctuation to zero, since zero is not far away.”

song of the dodo
Deterministic factors are those involving straightforward cause-and-effect relations that to some extent can be predicted and controlled: hunting, trapping, destroying habitat, introducing new animals that compete with or prey on existing ones, etc.

Stochastic factors “operate in a realm beyond human prediction and control, either because they are truly random or because they are linked to geophysical or biological causes so obscurely complex that they seem random.” We’re talking things like weather patterns, epidemic disease, infestation of parasites, forest fires, etc. Each might cause a downward fluctuation in the population of some species.

In Song of the Dodo, David Quammen gives the following illuminating example.

Think of two species that live on the same tiny island. One is a mouse. Total population, ten thousand. The other is an owl. Total population, eighty. The owl is a fierce and proficient mouse eater. The mouse is timorous, fragile, easily victimized. But the mouse population as a collective entity enjoys the security of numbers.

Say that a three-year drought hits the island of owls and mice, followed by a lightning-set fire, accidental events that are hurtful to both species. The mouse population drops to five thousand, the owl population to forty. At the height of the next breeding season a typhoon strikes, raking the treetops and killing and entire generation of unfledged owls. Then a year passes peacefully, during which the owl and the mouse populations both remain steady, with attrition from old age and individual mishaps roughly offset by new births. Next, the mouse suffers an epidemic disease, cutting its population to a thousand, fewer than at any other time within decades. This extreme slump even affects the owl, which begins starving for lack of prey.

Weakened by hunger, the owl suffers its own epidemic, from a murderous virus. Only fourteen birds survive. Just six of those fourteen owls are female, and three of the six are too old to breed. Then a young female owl chokes to death on a mouse. That leaves two fertile females. One of them loses her next clutch of eggs to a snake. The other nests successfully and manages to fledge four young, all four of which happen to be male. The owl population is now depressed to a point of acute vulnerability. Two breeding females, a few older females, a dozen males. Collectively they possess insufficient genetic diversity for adjusting to further troubles, and there is a high chance of inbreeding between mothers and sons. The inbreeding, when it occurs, tends to yield some genetic defects. Meanwhile the mouse population is also depressed far below its original number.

Ten years pass, with the owl population becoming progressively less healthy because of inbreeding. A few further females are hatched, precious additions to the gender balance, though some of them turn out to be congenitally infertile. During that same stretch of time the mouse population rebounds vigorously. Good weather, plenty of food, no epidemics, genetically it’s fine—and so the mouse quickly returns to its former abundance.

Then another wildfire scorches the island, killing four adult owls, and, oh, six thousand mice. The four dead owls were all breeding-age females, crucial to the beleaguered population. The six thousand mice were demographically less crucial. Among the owls there now remains only one female who is young and fertile. She develops ovarian cancer, a problem to which she is susceptible because of the history of inbreeding among her ancestors. She dies without issue. Very bad news for the owl species. Let’s give the mouse another plague of woe, just to be fair: a respiratory infection, contagious and lethal, causes eight hundred fatalities. None of this is implausible. These things happen. The owl population—reduced to a dozen mopey males, several dowagers, no fertile females—is doomed to extinction. When the males and the dowagers die off, one by one, leaving not offspring, that’s that. The mouse population fluctuates upward in response to the extinction of the owls, a rude signal that life is easier in the absence of predation. Twelve thousand mice. Fifteen thousand. Twenty thousand. But while its numbers are so high it will probably overexploit its own resources and eventually decline again as a consequence of famine. Then rise again. Then decline again. Then …

The mouse population is a yo-yo on a long string. Despite all the accidental disasters, despite all the ups and downs, the mouse doesn’t go extinct because the mouse is not rare. The owl goes extinct. Why? Because life is a gauntlet of uncertainties and the owl’s population size, in the best of times, was too small to buffer it against the worst of times.

Still curious? Read The Song of the Dodo.

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