Wasps: artists or robots?

November 15, 2010 • 5:13 am

by Matthew Cobb

[Continuing my lazy practice of re-posting material from elsewhere in the blogosphere and bringing it to the attention of WEIT readers, here’s one I posted last week over at Pestival (the insect arts festival – yes, honest!  Go look!)]

In case you weren’t listening to BBC Radio 4 at 06:15 am the other Sunday morning, I thought I would present to you the case of one of nature’s artists, the potter wasp. This small solitary wasp was the subject of the excellent Radio 4 programme The Living World. Anyone, anywhere in the world, can listen to it again here:

The female wasp makes a little clay pot about 1cm across, with a small hole in the end. She lays an egg in the pot, and then crams it full of living, semi-paralysed caterpillars which her offspring can eat. You can see quite how small the pot is in this photo from the BBC website, by Andrew Dawes. The “pot” is the tiny white thing underneath the middle finger!

[EDIT: The following (clearer) picture was taken by WEIT reader TrineBM (see comment 2 below)]:

According to Wikipedia (so it must be true, no?) the great entomologist Karl von Frisch, who was the first to study the honey bee’s waggle dance, claimed that the shape of the potter wasps’s pot inspired native American pottery designs. Quite how one could know that was true (or not) is hard to say – and what about other pots from round the world that look pretty much the same?

But is the wasp really an artist? Does it know what the pot should look like? John Walters, who’s been studying the potter wasps on this Devon heath for the last four years, says that he thinks each wasp has a different style – some pots are symmetrical, others have distinct twists. That doesn’t mean to say they know what they’re doing. Indeed, it seems certain they do not.

One of my favourite studies of animal behaviour was carried out on a potter wasp in 1978 by Andrew P. Smith, then of the University of Sydney. On the other hand, I seem to be one of very few people who rate this work – it has only been cited 13 times in the last 32 years. I feel your pain Dr Smith!

Andrew’s wasp – Paralastor – makes a rather more elaborate nest than the Devon potter wasp, a kind of odd umbrella shape, made up of a mud column and a bell-shaped entrance, leading to an underground chamber where the larva can munch its way through its living lunch, as seen here:

This picture shows the female wasp in action:

So how does she know what to build? Construction takes place in stages:

But does she have an image of what the final nest should look like? Or does she simply know that she’s carried out a series of behaviours and simply do them in sequence? The answer to both these questions is “No”.

Through a series of experiments involving changing the ground level, or altering the angle of the column, or making holes at various points, Smith was able to show that the wasp in fact proceeds by a series of steps, each of which is induced by a particular stimulus. If she sees a hole, she makes a column – even if this ends up with a bizarre double-umbrella nest:

The conclusion of the paper – apart from a lot of very tired and confused wasps – is this rather neat flow diagram, showing how the wasp decides what to do next:

So the wasp is not an artist, it’s more like a simple robot, carrying out a task when the appropriate conditions are provided. Less romantic, but still amazing!

Andrew P. Smith (1978) An investigation of the mechanisms underlying nest construction in the mud wasp Paralastor sp. (Hymenoptera: Eumenidae). Animal Behaviour 26:232-240.

The evolution of cat coat patterns

October 27, 2010 • 8:35 am

Why are some species of kittehs plain, while others have spots, stripes, or more elaborate patterns? A provisional answer comes from a new paper by William Allen et al., “Why the leopard got his spots: relating pattern development to ecology in felids”, in the Proceedings of the Royal Society.  The paper’s title, of course, comes from Rudyard Kipling’s Just So Stories.  And the short answer is this: the coats of wild cats help camouflage them, and what pattern evolves depends on where the species lives.

The simple answer comes from a rather elaborate analysis.  The authors set up the paper with what I think is a good specimen of clear scientific writing.  It’s not Joyce, of course, but these guys know how to write. I love the alliteration of “flanks of felids” and the breeziness of “pounce or quick rush.”

The patterns displayed on the flanks of felids are intriguing in their variety. Previous studies of the adaptive function of cat coat patterns have indicated that they are likely to be for camouflage rather than communication or physiological reasons [1,2]. The primary hunting strategy of felids is to stalk prey until they are close enough to capture them with a pounce or quick rush [3,4]. As hunts are more successful when an attack is initiated from shorter distances [5,6], cats benefit from remaining undetected for as long as possible and camouflage helps achieve this. Many smaller cats are also likely to be camouflaged for protection from predation [7].

The authors first note that others before them have suggested—and supported with some data—the idea that spotted or stripey cats live in forested habitats, and plain cats in open habitats.  But they quantify this “complexity” by doing a developmental analysis of coat patterns on pictures taken from the internet.  I won’t go into the details, but they match the photographs with patterns generated from a mathematical model in which pattern results from the interaction of two diffusible chemicals along gradients of the body.  Given a model that matches an existing pattern (they used 35 species of felids), they could then encompass “pattern” in the mathematical constants involved in generating it.  They could then correlate these constants with various aspect of cat ecology: where they live, preferred times of activity, how big they are, what they eat, and how social they are.

Here’s an example of a cat that came out “plain” in their analysis: the caracal (Caracal caracal), from Africa and the Middle East:

Nine of the 35 species were considered “plain.” Here’s a cat considered “patterned and complex”: the gorgeous clouded leopard (Neofelis nebulosa), from southeast Asia:

Sixteen species were considered patterned, with four of these, including the clouded leopard, as “always complex.”  The other ten were considered “variable”,” since there was polymorphism: individuals within a species can look quite different.

The results?

  • Pattern itself, whether complex or not, was significantly associated with habitat, with more patterned cats in more “closed” habitats (forest, jungle, etc.).  Plain cats are found in open habitats like grasslands, deserts, and mountains.
  • More irregular patterns, like the cloud leopard, are significantly associated with tropical forests and other “closed” environments.
  • “The more time cats spent in trees, the more likely they were to be patterned.”
  • Pattern polymorphism, as in the melanism of “black panthers,” was significantly associated with living in temperate forests that vary seasonally and also with habitat generalism. This supports the idea that “disruptive selection,” that is, selection for different patterns in different places, maintains the intra-specific variation in coat color.
  • There were a few “outliers,” or exceptions—cats that had patterns not fitting into the habitat correlations given above.  One is the very rare bay cat (Catopuma badia; I’ve posted on it before), which is plain though it lives in tropical rainforest:

And another outlier is the black footed cat of Africa (Felis nigripes), which is patterned though it lives in open habitat (savannah, grassland, and semi-desert):

The authors note that the tiger is the only wild cat with vertical stripes, and the common notion that this camouflages them in grassland is unfounded: tigers don’t live in grasslands.

The conclusion, then, is that the patterns of cat coats reflect, in large degree, selection for camouflage in their natural habitats. This camouflage almost certainly evolved to hide them from prey, and, in smaller cats, predators as well.

I love the inclusion of a Kipling quote in their conclusion (reference “45” is to the Just So Stories):

These findings support the hypothesis that felid flank patterns function as background matching camouflage. Evolution has generally paired plain cats with relatively uniformly coloured, textured and illuminated environments, and patterned cats with environments ‘full of trees and bushes and stripy, speckly, patchy-blatchy shadows’ [45].

Now the sample size—35 species—is not large, and some of the associations were barely significant from a statistical standpoint.  This could reflect the low power of tests in small samples. Nevertheless, the study offers a good working hypothesis for the evolution of pattern not just in cats, but other species that “need” to be cryptic.  What remains to understand are those outliers like the bay cat, and also the existence of developmental change of pattern, in which some species are patterned when young and lose the patterns when they get older.  Lions, which are spotted as cubs, are a good example of this:

This change might not be adaptive per se, but simply be an atavism: a holdover from an ancestral spotted pattern that still persists in the young.

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Allen, W. L., I. C. Cuthill, N. E. Scott-Samuel and R. Baddeley. 2010.  Why the leopard got his spots: relating pattern development to ecology in felids.  Proc. Roy. Soc. B online: doi: 10.1098/rspb.2010.1734

Shark jaws

October 23, 2010 • 5:50 am

Here are two more photos from my immensely edifying visit to Jim Krupa’s lab at The University of Kentucky.  They show the extreme diversity of morphology that evolution can produce in a single group.

The first shows the jaw of what I remember as a tiger shark, Galeocerdo cuvier.  National Geographic notes that “They have sharp, highly serrated teeth and powerful jaws that allow them to crack the shells of sea turtles and clams. The stomach contents of captured tiger sharks have included stingrays, sea snakes, seals, birds, squids, and even license plates and old tires.”

The rows of teeth are lined up, waiting in the wings, to be replaced after one on duty is lost. The teeth aren’t embedded in the jaw, but merely in the gum tissue.  Wikipedia has a good article on them.

Sharks are in the class Chondrichthyes:  they have cartilage rather than bone.  The subclass Elasmobranchii includes sharks, skates and rays.  And the tiger shark is in the largest order of elasmobranchs, the Carcharhiniformes.

And here’s one of the weirdest elasmobranchs—the jaw of the Port Jackson shark (Heterodontus portusjacksoni), endemic to Australian waters.  It’s in the order Heterodontiformes (“bull sharks”), distinguished, among other things, by having the mouth completely in front of the eyes. The “Heterodontus” part of the genus name means “different teeth,” and that’s indeed what you see, spectacularly, in the jaw.  Having differentiated teeth in the jaw is very rare in sharks:

The small teeth in front are for grabbing and piercing, the ones at the rear for grinding up stuff, especially molluscs.  The Florida Museum of Natural History site notes:

This species feeds primarily on echinoderms, crustaceans, molluscs, and some small fish. Sea urchins and large gastropod molluscs are noted in almost every study on the diets of Port Jackson sharks. Stomach contents are typically ground up too small for full identification, thus leading researchers to believe Port Jackson sharks grind their food thoroughly before swallowing. This is also supported with juvenile diets, since it has been noted that juveniles eat more soft-bodied animals, and contain less molar-like teeth.

Here’s what the jaws look like in situ:

For $750 you can actually buy a Port Jackson shark for your aquarium, but I’m not sure why anyone would do that, as they grow over five feet long.

You can see the variety of sharks’ teeth here, and if you’re into buying recent or fossil teeth, here’s a place to start,

Adult fly mimics ant larva

September 24, 2010 • 8:30 am

This is the kind of stuff I love to find in my inbox in the morning.  I work on flies, and I’ve never seen or heard of these ones until Matthew Cobb posted about them in his email Z-letter this morning. Look at the creature in the top photo.  Looks like a larva, right? In the bottom photo you can see the same beast with some larvae of the army ant Aenictus.

It’s not a larva at all: it’s an adult fly that mimics ant larvae.  To be precise, it’s a phorid fly, Vestigipoda longiseta, from southeast Asia. (“Vestigipoda” means “vestigial legs,” which these guys have.  That, of course, is  evidence that these things evolved rather than being created.)

The long “grubworm” part of the body is simply the enormously elongated and unpigmented abdomen of the adult.  The head and thorax are the dwarf structures at the left-hand side of the top photo.  This has all evolved from an ancestor that looks pretty much like the flies you know.

You can imagine why natural selection would favor this resemblance: the ants tend and feed the larvae, and mistake the flies for their own brood.  It’s a lifetime of free lunches!  The ants also protect the flies and carry them (like they carry their own larvae) when a colony is on the move.  Here’s an adult of V. longiseta being carefully carried by an Aenictus ant:

Why can’t the ants detect these intruders?  Well, they’re not terribly harmful, getting just a bit of food from the colony, so there’s probably not strong selection to weed them out.  Ants, of course, have pretty bad vision, so they probably can’t see the intruders as different from their own brood. Matthew Cobb hypothesizes, and I agree, that there’s probably chemical mimicry going on here as well: the hydrocarbon molecules on the fly’s cuticule may well resemble the compounds on ant larvae, so that the ants, who “taste” these hydrocarbons, are fooled by chemical mimicry. This could easily be settled with a bit of gas chromatography.

There are several species of Vestigipoda in southeast Asia.  Here’s a shot of the head (right), thorax and first abdominal segment of another species, a Vestigipoda maschwitzi female (from Disney et al, 1998).  You can clearly see the features of a fly.

This is not, as Christopher Taylor at Catalogue of Organisms points out, a case of neoteny—that is, of juvenile flies becoming sexually mature. (An example of that is the axolotl salamander, Ambystoma mexicanum, in which gilled juveniles are able to reproduce.)  No, these phorids have the regular larval stages of flies, but then go through normal metamorphosis, winding up as an adult with ant-larval features.

Curiously, all known larval mimics of Vestigipoda are females.  Where are the males?  Taylor suggests that they may be “normal” flying flies, in which case they’d have to somehow sneak into the ant colonies to mate.

Phorids are just plain weird: they’re among the smallest flies, many are wingless, and there are some vicious parasites among them.  Have a look at this one, which is about the most gruesome fly I know of.  Its larvae live inside ants, crawl into their heads, decapitate them, and then use the empty head for protection during pupation:

There’s simply no end to the wonderful stuff evolution comes up with.  There are tons of weird flies out there; I’m planning “Fly Week” when I return.

h/t:  Catalogue of Organisms

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Disney, R. H. L., A. Weissflog & U. Maschwitz. 1998. A second species of legless scuttle fly (Diptera: Phoridae) associated with ants (Hymenoptera: Formicidae). Journal of Zoology 246 (3): 269-274.

Maruyama, M., R. H. L. Disney & R. Hashim. 2008. Three new species of legless, wingless scuttle flies (Diptera: Phoridae) associated with army ants (Hymenoptera: Formicidae) in Malaysia. Sociobiology 52 (3): 485-496.

Bad breath fells aphids

August 20, 2010 • 5:43 am

Friday science quickie:  a new paper in Current Biology reports an intriguing adaptation: the breath of mammalian herbivores induces aphids to drop off plants, saving them from being eaten along with the leaves.

Three biologists at the University of Haifa in Israel noticed that two species of aphids, the pea aphid (Acyrthosiphon pisum) and Uroleucon sonchi,  dropped off their plants when they were about to be ingested by a goat or a lamb.  Here’s a photo:

This escape behavior is probably adaptive, because although dropping off the plant risks death by starvation and desiccation, it surely give you more of a chance than being eaten by a herbivore.

The authors tested whether the appearance of a shadow over the plant, or shaking of the plant itself from plucking leaves, could cause this behavior  Shaking caused a moderate drop, but nowhere near as big as herbivore breath.  Nor did the aphids drop when faced with a natural predator, the ladybug (Coccinella septempunctata).   So the authors made an artificial breath machine, which controlled temperature, humidity of the airstream, and presence of chemicals in the airstream:

The result:  no chemicals, including carbon dioxide, acetone, etc., increased the aphid drop, nor did they in mixture.  Bovine nasal secretions added to the air didn’t do anything, either.  Nor did higher airstream temperature or higher humidity at ambient temperature.  But the aphid drop really took off when they increased both the temperature and humidity of the airstream.  It was the combination of these two factors, then, that the aphids used as a dropping cue.

This fleeing behavior in response to mammal breath is, so far, unique.  Other parasites, like ticks and mosquitoes, can detect and home in on exhaled carbon dioxide and body head, but using mammalian (and perhaps bird) cues to flee hasn’t been seen before.  Of course, nobody’s really looked for it before (this study resulted from a fortuitous observation), and I’ll bet that there are similar cases in other species.

One question: has this behavior evolved in recent times, when humans introduced foraging cows and goats? Or did aphids have mammalian enemies in more ancient times? The authors don’t discuss this.

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Gish, M., A. Dafni, and M. Inbar. 2010.  Mammalian herbivore breath alerts aphids to free host plant.  Current Biol. 20:R628-R629.

Why eyespots?

June 30, 2010 • 6:52 am

While listening to talks at the evolution meetings, I’ve mentally divided them into two groups: what I call “general” versus “anecdotal” research.  The former seeks general laws of evolution that apply across diverse species.  “Haldane’s rule” is one example:  the observation that if, in a cross between two species, only of the two sexes of hybrid offspring is sterile or inviable, it’s nearly always the heterogametic sex (males in mammals and many insects, females in birds and lepidoptera). I’ve spent a lot of years trying to explain that one. Another “law” is the repeated observation that if only one sex in a species is ornamented or brightly colored, it’s almost invariably the male sex.

“Anecdotal” research—the name is not meant disparagingly—seeks to find the evolutionary basis of a single phenomenon, often in a single species.  The “panda’s thumb”, made famous by Steve Gould, is a familar example.  In this case, a herbivorous bear has evolved a rudimentary opposable “thumb” by modifying the radial sesamoid bone of the wrist.  The thumb helps strip leaves from bamboo, the only item on the panda menu.

Both strategies are essential to answer the question, “How has evolution produced the marvels of nature?”  But young people at this meeting seem to be pursuing the “generalist” strategy, perhaps sensing that career rewards are more likely to come if you answer Big Questions rather than concentrating on a single system.

A new perspective piece by Dan Janzen and his colleages in PNAS straddles the boundary between these two areas. It takes a single element in the color pattern of caterpillars and pupae of Lepidoptera—the presence of false eyespots—and floats a theory to explain this group-restricted pattern.

Janzen, perhaps the world’s finest field naturalist, has spent much of his life studying the insects of Costa Rica, especially in Guanacaste Province in northwest Costa Rica.  (I had the privilege of being one of Dan’s students in a Tropical Ecology course in Guanacaste in 1973.) He and his colleagues noticed, as others had before them, that many of the Lepidoptera (butterflies and moths)  in the neotropics had markings on the larvae (caterpillars) and pupae that looked a lot like eyes.  Here are some caterpillars with eyespots, taken from the paper:

And here are nonmobile pupae with eyespots:

Nice, eh?  Biologists have reflected on the existence of these eyespots, suggesting that they evolved because they enhance survival.  How? By fooling predators, mostly birds, who mistake the “eyespots”  for their own enemies—snakes, lizards, predatory birds, and some mammals—and flee in fear.  The insect with the eyespots thereby avoids being eaten.

It’s clear that the eyespots have something to do with predation, because in many cases they’re displayed only when the larva is disturbed or detected by a potential predator.  Here’s one example, with the caption (taken from the paper):

The 7-mm-wide pupa of Cephise nuspesez (23) (Hesperiidae), a Costa Rican skipper butterfly as itappears to a foraging bird that (Upper) has poked into the front of the rolled leaf shelter constructed bythe caterpillar or (Lower) has opened the roll from above. When disturbed, this pupa rotates to present its face to the open end of the leaf roll.

That sure looks as if it would frighten a foraging bird that was investigating a leaf.

Here’s another example of how eyespots are displayed when a caterpillar is detected (note that this adaptation is twofold: the eyespot itself but also the evolved behavior that displays it only in a certain context).  The caption is from the paper:

The 50-mm-long last instar caterpillar of Costa Rican Ridens panche (Hesperiidae) at the moment when its leaf shelter is forced open (Upper) and a few seconds later (Lower), when it presents glowing red false eye spots directed at the invader and glowing lemon-yellow eye spots in the dark of the cavernbehind. Both kinds of false eyes are thrust at the leaf roll entrance until the invader leaves.

So far so good.  Janzen et al. are not the first to suggest that eyespots evolve to protect lepidopterans from predation.  But they go further, and suggest that the birds’ avoidance of insect eyespots is often innate (that is, a hard-wired genetic behavior that is the product of natural selection) rather than learned.

A bit of background.  Some forms of mimicry, in which an edible species of insect mimics another species that is both brightly colored and repugnant to predators, involve predator learning.  When a hand-reared and naive bird eats a ladybug for the first time, it noms it down and then, realizing how dreadful it tastes, spits it out.  You can show in the lab that after one or a few such episodes the bird learns to avoid the brightly spotted pattern of the lady bug. And, it will also avoid tasty insects that have evolved patterns that resemble the ladybug. (This resemblance has evolved in many species that birds find tasty, including cockroaches and beetles.)

This form of mimicry, in which an edible species evolves to physically resemble an inedible one, is called Batesian mimicry, after the Amazonian naturalist H. W. Bates.  Its evolution depends on the predator being able to learn that an insect is inedible, and then generalizing that experience to avoid other insect species with similar patterns.

Janzen et al. suggest, however, that the eyespot mimicry (lepidopteran patterns mimic bird-predator eyes) is based not on the predator learning to avoid the eyespots, but evolving to avoid the eyespots.  The state their reason succinctly:

[T]he bird that must learn to avoid an eye is not long for this world.

In other words, the evolution of “eye avoidance” (which generalizes to eyespot avoidance) is likely to be innate rather than learned, for it’s hard to learn to avoid an eye.  If you encounter the eye of an owl or a snake, and don’t flee right away, you’re dead. No learning can occur. On the other hand, the higher survival of individuals who flee at the sight of an eye would select for an innate avoidance of things that look like eyes.

Once that’s evolved in an insect-eating bird, it sets the stage for the evolution of eyespots in caterpillars and pupae, which gain survival benefits from the birds’ innate avoidance of anything eyelike. Janzen et al. call this phenomenon, which has apparently caused the evolution of eyespots in hundreds of diverse lepidopteran species, “diffuse seletion.”

Janzen et al. don’t mention this, but their theory about innate versus learned avoidance is eminently testable.  All you have to do is hand-raise, from eggs, some of the birds known to flee from eyespots.  If, on first encountering a pupa or caterpillar with an eyespot, they get startled and flee, then their aversion must have been innate rather than learned.

This kind of experiment was done by Susan Smith in 1975, showing that birds who avoid the black, yellow, and red striped pattern of coral snakes do so innately, not through learning (indeed, it would be hard to learn since an encounter with a coral snake is likely to be fatal).

Explaining eyespots may not yield the professional cachet of explaining something like Haldane’s rule, but the real joys of evolutionary biology are found more often in the particular than in the general.

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UPDATE: In the comments, Naturalistbiologist points out the scary resemblance of the Gaudy Sphinx caterpillar to a snake.  Just to show you how far caterpillar mimicry can go, have a look at it:

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Janzen, D. H., W. Hallwachs, and J. M. Burns.  2010.  A tropical horde of counterfeit predator eyes. Proc Nat. Acad. Sci. USA 107:11659-11665.

Smith, S. M. 1975. Innate recognition of coral snake pattern by a possible avian predator. Science 187: 759–760.

Polymorphism in vertebrates

March 26, 2010 • 1:04 pm

by Greg Mayer

Darwin’s theory of evolution (and ours), unlike that of Lamarck, is variational, rather than transformational: the process of evolution is a change in frequency of different variants within a population, not a transformation of the individuals.  Darwin thus made the origin, nature, and inheritance of variation key problems for biology; indeed, for much of the 20th century, evolution and genetics were often taught as a single course at universities.

One of the most distinctive sorts of variation is polymorphism, in which two or more discontinuous forms are found in a single species (this is distinct from sexual or age related variation). Darwin himself pioneered the study of polymorphisms. Such discontinuous variation often has a simple genetic basis, with allelic variation at one genetic locus accounting for all (or most) of the variability.The color polymorphism in peppered moths (Biston betularia) is a well known and well studied case involving industrial melanism, in which light and dark forms are adapted to polluted and unpolluted environments, respectively. A well known case of polymorphism in vertebrates are the two color phases of Cuban sparrow hawk (Falco sparverius sparverioides). This case is not well studied, though, and we know nothing about the genetics, nor the adaptive significance (if any) of the polymorphism.

Light and rufous phase male Cuban sparrow hawks (Falco sparverius sparverioides).

A polymorphism in vertebrates that many Americans and Canadians are familiar with are the melanistic and gray forms of the gray squirrel (Sciurus carolinensis). The most frequent color form is gray, but blackish or dark brownish individuals are widely distributed, and in places quite frequent. I have seen them in Illinois (Cook County), Wisconsin (Racine and Kenosha Cos.) and Michigan (Ingham Co.), and also on the campus of Princeton University. (I was told at Princeton that, during football season, black squirrels are captured, and orange stripes applied to them, so that they resemble diminutive arboreal tigers, the tiger being Princeton’s mascot.)

A demonic gray squirrel (locally known as 'yard dogs'), Annapolis, MD, 23 June 2008.

A much less common color morph is the leucistic or albinistic form, which is whitish, cream or yellowish. They are famously common in Olney, Illinois (due to an introduction of two albinistic individuals to an area previously lacking any gray squirrels at all), and also occur regularly in Stevens Point, Wisconsin, but I had never seen one before my recent trip to Washington, DC, where I saw one on the tree right across from the steps on the Mall entrance to the USNM.  (The picture was taken through a bus window.)

Leucistic or albinistic gray squirrel, Washington, DC, 16 March 2010.

Vertebrate polymorphisms are often less well understood than those of invertebrates, because their generally greater size and longer generation times make experimental study more difficult. Melanism in squirrels, for example, has been related to thermoregulation and fire frequency, but no thoroughly compelling explanation has been found. One exception to this is coat color variation in mice of the genus Peromyscus, where coat color seems to be an adaptation for camouflage in varying environments.

Light and dark forms of Peromyscus polionotus from sandy and dark soils (P. p. leucocephalus on the left, P. p. polionotus on the right, I think).

In the 1930s, F.B. Sumner conducted classic field and lab studies on light colored mice living on sandy soils and dark mice on dark soils. Unlike the melanistic and albinistic squirrels, which are variant individuals within a populations, there is an element of geographic variation in the mice, which live in distinct, though adjacent, places. Sumner’s studies showed that there were several (not just one) genetic loci involved in coat color, and the color forms intergrade where their habitats meet and they interbreed. Hopi Hoekstra of the Museum of Comparative Zoology is currently conducting exciting studies of some of the same species studied by Sumner.

Although the mice occur in distinct modal forms (white vs. brown), the intergradation where they meet shows an underlying continuous variation. The frogs below show that although we can pick out distinctly different individuals, the range of pattern from plain to mottled to striped makes it difficult to recognize a small number of discrete color morphs, and the variation approaches a continuous dictribution. Such continuous variations were thought by Darwin, and most biologists today as well, to be important raw material for the evolutionary process.

Leotpdactylus albilabris from Isla Vieques.