Mapping evolution

“Nutcracker” fish shows evolution in action

In biology, odd is awesome. Charles Darwin, famously, struggled with the peacock’s outlandish tail. You might have wondered why the rhinoceros has a horn. We wonder why the narwhal has a tusk-like tooth and looks like an underwater unicorn.

Christopher Martin, a Ph.D. student at the university of California at Davis, wants to know why the common pupfish, found in wetlands from Massachusetts to Venezuela, does not share its ponds with related pupfish species.

ENLARGE

Small, silver fish swimming near bottom of water body, surrounded by short grasses and suction-cup-like plants.

Image courtesy of Chris Martin
This generalist pupfish, in its natural habitat on San Salvador Island, Bahamas, doesn’t have much of a nose. Check out the impressive hood ornaments on the closely-related fish down below!

The lone exception occurs in the Bahamas, where two sister pupfish species evolved from a common ancestor in ponds that are just 10,000 years old.

Three pupfish species live in the pond in question, says Martin, who was first author of the new study:

one generalist that eats a wide variety of food, including seaweed

a parasite that (ecch!) eats scales from other pupfish

a shellfish-eating carnivore with a honking big “nose”

ENLARGE

Two fish. Left: iridescent brown with enlarged bottom jaw. Right: light orange with enlarged nose structure.

Images courtesy Tony Terceira
Left: The Cyprinodon scale-eater is a unique pupfish that eats scales from other fish. Right: Cyprinodon durophage is a specialist pupfish with unique, protruding nasal appendage suited to eating shellfish (clams, anyone?). These pupfish are endemic to San Salvador Island, Bahamas.

The shellfish eater “is bizarre. It’s essentially a fish with a nose; it has a swollen nasal region and the jaw tucks up underneath,” says Martin, and “no one knows what it is used for. Possibly the nose stabilizes the jaw to help crush prey, or females use it to discriminate among males, or it could be a sensory organ. The nose is not just a nutcracker.”

These pupfish are a recent example of adaptive radiation, a rapid evolution of species that occurs after an organism reaches new habitat with empty ecological niches. But why do distinct new species arise, instead of a mishmash of in-between traits?

Trouble is…

How, exactly, does adaptive radiation take place? Offspring of genetically dissimilar parents usually lack the abilities of their parents, and die out, which makes it difficult to transition toward a new ability, like stripping scales or shucking clams.

To study how changes in phenotype (genetically determined behavior and structure) affect survival, biologists create graphs that look like mountains maps.

Survival of fish in wild plotted against jaw shape shows higher survival for two of the three fish studied.

San Salvador Island, Bahamas, courtesy Christopher Martin
This plot relates the survival of three types of pupfish (vertical axis) to the shape of their jaws and bodies (horizontal axes). These fish resulted from adaptive radiation during the past 10,000 years.

On these graphs, peaks show phenotypes with enough offense, defense and presumably reproductive ability to pass along their genes to posterity. But when diverse individuals mate, the hybrids must “jump between the peaks.” They may form a new species, but are more likely to drop into “death valley.”

ENLARGE

Open pond surrounded by vegetation, with study plot at the edge enclosed by black netting supported by white, plastic pipe.

Image courtesy of Chris Martin
Martin used this field enclosure, in Crescent Pond on San Salvador Island, Bahamas.

To figure out how two new pupfish evolved from their common ancestor (the generalist shown in the top photo), Martin cross-bred members of the three pupfish species. (The species could cross-breed because they are still closely related, after such a brief evolution.)

But the offspring were oddballs, says Martin, who worked with Peter Wainwright, a professor of evolution and ecology at Davis. “Eighty percent of the hybrids look nothing like what you find in the wild.” When he returned, the hybrids that had survived “nearly exactly matched the original species.” In other words, there was little room for blended phenotypes; these fish occupied the deadly lower regions of the graph.

Adaptive radicals

The study addresses a mystery from Hawaii and the Galapagos Islands, hotbeds of adaptive radiation. “We have no idea” why some birds, through adaptive radiation, left many related species, while other species did not, Martin says.

The new maps could explain the rarity of specialists in pupfish ponds, Martin says. “When people talk about adaptive landscapes, classically, they think the population should move uphill” to a higher level of adaptation.

But even though the shellfish eaters were more fit in the Bahamas, “The generalists are isolated by a ‘fitness valley’ between them.”

“It’s remarkable,” Martin says. The experiments were done in small pens, “and this means there are two ways of being a pupfish and surviving, even in this small enclosure.”

— David J. Tenenbaum

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Terry Devitt, editor; S.V. Medaris, designer/illustrator; David J. Tenenbaum, feature writer; Amy Toburen, content development executive; Emily Eggleston, project assistant

Bibliography

  1. Multiple Fitness Peaks on the Adaptive Landscape Drive Adaptive Radiation in the Wild, Christopher H. Martin and P.C. Wainwright, Science, 11 Jan. 2013.
  2. Salt or fresh? How fish survive in different types of water
  3. Taking the long view: Fish as they first appeared on earth
  4. What’s the latest news on fish evolution?
  5. The Story of the Prehistoric Fish

Tracking traveling toads

POSTED FEBRUARY 4, 2010

The genes of an invading toad

Why do some animals steam-roll across the landscape, commanding new territory in the manner of Genghis Khan, while others skulk around a tiny patch of marsh?

The question can also be applied to smaller groups of animals, like the toads. At one extreme, the spray toad lives only in the mist of one waterfall and has gone extinct in its native Tanzania. Meanwhile, the cane toad, a monster native of South America that was deliberately distributed to control insects on farms, has colonized Australia and Caribbean and Pacific islands, where it is busily crowding out native animals.

Closeup photo of brown toad sitting in grass with tall tree in background, toad in a resting position

The cane toad is an ecological pest in Australia, but it carries a full set of genes that enable it to occupy new habitat.

Both species are among the 500-plus members of the family bufonidae, called the “true toads.” But what distinguishes toads that can dominate new landscapes from those that must struggle to survive, and what can that tell us about how species form from their ancestors?

In a study published this week, Ines Van Bocxlaer, of the biology department at Vrije University in Brussels, identified “range expansion” traits that would, logically, make for successful invaders:

Poison glands that make the skin toxic to predators

The ability to survive dry conditions with an intermittent water supply

A large body with plenty of energy-storing fat

Heavy egg production

Image courtesy Franky Bossuyt
The Common Indian Toad (Duttaphrynus melanostictus), an optimal range-expansion phenotype that originated from tropically-adapted ancestors endemic to the Western Ghats mountain range of the Indian subcontinent.

The making of a new species

“We chose characteristics that might be related to being able to disperse,” says Franky Bossuyt of Vrije University, the study’s corresponding author. “If they don’t need too much water, or are poisonous, that’s an advantage.”

Van Bocxlaer and colleagues correlated the range expansion traits with the size of habitats occupied by particular species, and concluded that all seven traits were “highly correlated” with the area occupied by the toads in their new homes, Bossuyt said.

The researchers produced a branched genetic tree that traces back to the ancestral toads in South America, which suggested that the range expansion traits were present when the toads began dispersing to new locations between about 37 million and 24 million years ago. Afterwards, these traveling toads branched into many of the species that survive today.

The species that now live in South America, however, have fewer of the range expansion traits. “We think it is the first time this was studied in this way, correlating the range-expansion characteristics and mapping them on a phylogenetic tree,” says Bossuyt.

Photo: Simeon
A sugar cane farm in Northern New South Wales, Australia. Cane toads were brought here to control insect pests, and then became pests themselves.

Traits tell tales

These results shine a beacon on a venerable evolutionary question: do new species arise before or after they begin occupying new ground? Which is more important for promoting the development of new species: new habitat, or the traits needed to occupy it?

“Links between geographic expansions and speciation have rarely been demonstrated,” says Carol Lee, an associate professor of zoology at the University of Wisconsin-Madison. “The authors first found a correlation between life history traits that might promote range expansion and current distribution, suggesting that such traits are plausible candidates for promoting range expansions.” Then they constructed a genetic tree of the apparent range-expansion traits, and found that the traits correlated with the transcontinental movements, adds Lee, who focuses on the genetics of invasive organisms.

Finally, the researchers calculated that species were forming extra-fast during the global colonization, Lee notes. “The authors argue that this coincidence suggests that range expansion itself might have been an important driver of diversification and speciation. Thus, they argue that this might be a case where dispersal ability might drive range expansions, followed by speciation.”

“Range expansion itself,” the researchers concluded, “was an important driver of diversification in bufonids.” In other words, animals that can adapt are more likely to invade and conquer new habitats.

Photo: Image courtesy Bert Willaert
The common European toad has all the talents needed to colonize new habitat, and is widespread in Europe.

Which came first?

The differentiation of newcomers into many different species is the standard explanation for the many unique species found in islands like Hawaii. Although this “adaptive radiation” is often thought to result from the availability of new ecological niches rather than the genetic talents of the arriving organism, the new study suggests that these genetic talents may need more focus.

Because the study looks at only one example of global expansion, “the co-occurrence of acceleration of speciation with global colonization could be purely coincidental,” says Lee. “Nevertheless, this study is an elegant attempt to test the links between range expansions and speciation.”

Although Bossuyt concedes that the study may not aid the battle against the pestiferous cane toad, “if people wanted to try again to introduce some other species, they could use this method to predict if it was good disperser or not, and thus whether it might be dangerous.”

David J. Tenenbaum

Bibliography

Gradual Adaptation Toward a Range-Expansion Phenotype Initiated the Global Radiation of Toads, Ines Van Bocxlaer et al, Science, 5 Feb. 2010.

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