University of California, Davis

Category: sticklematt

Stickleback attack (part 1)

Since our last video posting, many of the videos on our lab’s Youtube channel have gone viral. As of this blog post, the video of Inermia vitatta has accrued over 120,000 hits and has been featured on TV programs and newspaper articles around the globe. Not bad for a small fish!

[youtube=http://www.youtube.com/watch?v=psdLbN7skg4]

Today’s video features the threespine stickleback, Gasterosteus aculeatus, feeding on a cladoceran (Daphnia pulex). If you have a short attention span like me, one of the first things you’ll notice from the video is how shiny the fish is. The reflective armor plates and large spines are a clue that this is a threespine stickleback from an anadromous population. Anadromous stickleback have a life history similar to a miniature salmon – they are born in freshwater, travel to the ocean, then return to freshwater to breed. Unlike salmon, anadromous stickleback do not necessarily return to their home stream to breed. Anadromous stickleback also look very similar to each other – an Alaska anadromous fish looks very similar to a California anadromous fish.

Sometimes, these anadromous stickleback will travel to a newly-formed lake or river, and instead of returning to the ocean, some fish will stay in freshwater, founding a new population of freshwater stickleback. Over time, this freshwater population will evolve to better match its new freshwater habitat.

These anadromous and freshwater populations are one of the reasons stickleback are such a good system for studying evolutionary biology. We can study the result of rapid evolution in the freshwater populations, and then turn around and study the anadromous fish that resemble the fish that founded the freshwater population. Studying ancestral and derived populations is one of the few ways – short of a time machine – that we can learn the dynamics of adaptation in natural populations.

If we study how this anadromous stickleback captures prey, and then study how freshwater stickleback catch prey, we can learn a lot about the process of adaptation. I’ve devoted much of my PhD work to studying this system, and I’ll be talking more about it in future posts.

Stickleback camouflage

This week, the Wainwright blog returns to a topic of perennial interest, the threespine stickleback. I will discuss a recent paper from the Schluter lab at UBC on color plasticity and background matching in stickleback.

To set the stage, it’s important to realize that from a stickleback’s perspective, “bird” is a four-letter word. Predation by diving birds like grebes and coots is commonplace in many freshwater stickleback populations. Unlike predatory dragonfly larva, which detect prey by vision and by water movement, diving birds generally detect their prey by sight alone. In other words, if you’re a freshwater stickleback, it’s very important that the top of your body blends in with your surroundings.

This stickleback didn't get the memo. (http://www.lifeontheslea.co.uk )

In this paper, Jason Clarke and Dolph Schluter tried to assay background matching capability between limnetic and benthic sticklebacks in Paxton Lake, British Columbia. First, they used a spectrometer to record the background color in the limnetic and benthic habitats. The open-water limnetic habitat was a bluish color, but the benthic habitat, which has more aquatic vegetation, tended to be more greenish. Additionally, the benthic habitat showed much more variation in color than the limnetic habitat.

After checking the background color, the authors painted two sets of cups, one designed to look like the limnetic background, and one designed to look like the benthic background. Then they put benthic and limnetic sticklebacks on each background, let them adjust their color for 15 minutes, photographed each fish, then measured how well each fish matched its background. They also did the same experiment again, but this time taking pictures every 20 seconds.

What did they find? Limnetic fish and benthic fish were equally good at matching the blue limnetic background, but limnetic fish were not as good at matching the green benthic background as benthics were. The time trial experiment helped to clear up what was going on: benthics rapidly adapted their colors to match the background, but limnetics were doing something different. Limnetic fish were cycling through different colors instead of fixing a particular color. Limnetics were more variable in color when viewed with a benthic background, but even on their “home turf” in the limnetic background, they still showed variation in color, but to a lesser degree.

The authors suggest that the patterns of color chance exhibited by benthics and limnetics are probably adaptive. Their spectrometer data indicates that the benthic habitat is more variable in color, and their background experiments show that benthics are better at rapidly changing their colors to match the background. The limnetic habitat, on the other hand, is much more uniform, so there would be little incentive for limnetics to evolve rapid color matching. However, limnetics may be adapting to their light environment in an entirely different way:  the  “flickering” exhibited by limnetics could be an adaptation to fluctuating light intensity in open water.

After reading this paper, I’m particularly curious what the color-matching abilities of the ancestral marine sticklebacks are like. If they resemble the limnetic, then this color matching ability will be another interesting benthic stickleback adaptation. It will be cool to see if it is possible to discern the genetic basis for this shift in plasticity.

Clark JM, Schluter D. Colour plasticity and background matching in a threespine stickleback species pair. Biological Journal of the Linnean Society. DOI: 10.1111/j.1095-8312.2011.01623.x

Stickleblog: Caught in the act

ResearchBlogging.orgThis week, I’m going to discuss a cool paper that came out of Dolph Schluter’s lab in 2008. The paper zooms in on a particularly interesting part of stickleback evolution, the transition between an ancestral marine form that breeds in fresh water to a population that lives in freshwater year-round.

Usually, (and this is one of the “color-coded for your convenience” things that make stickleback a fantastic model system) you can get a good idea where a stickleback is from by looking at its armor plates. Stickleback from marine habitats tend to have a full complement of plates, whereas sticklebacks from freshwater habitats will have few to no plates:


Stickleback armor plate phenotypes: fully plated (top), partially plated(middle), low plated(bottom)

The authors sorted through hundreds of marine stickleback to find fish that had intermediate numbers of plates, which signified that they were heterozygotes for the gene that governs plate number, Eda. These fish were placed in experimental ponds and allowed to breed. Because the fish were heterozygotes for Eda, they produced offspring with high, medium, and low plates, which gave the authors a chance to observe if natural selection favored the low-plated form in freshwater.

In each pond, the frequency of the low allele increased over time, and in a similar way. There was a slight dip when fish were very young, but then frequency increased until the fish reached breeding condition. Interestingly, fish carrying the low allele grew faster and reached breeding condition sooner than fish carrying the high allele, probably because building armor plates takes energy that could be spent on growing more quickly.

The story is more complicated than that, though – not only is there a period early in life where the high allele appears to be favored, but there is also a point where fish with intermediate plates have the highest fitness, which is difficult to explain. The authors raise the possibility that the Eda gene that controls plates in stickleback may affect other traits (pleiotropy). Either way, it looks like even the most well-understood stickleback phenotype has more to tell us.

Barrett, R., Rogers, S., & Schluter, D. (2008). Natural Selection on a Major Armor Gene in Threespine Stickleback Science, 322 (5899), 255-257 DOI: 10.1126/science.1159978

Stickleblog: Sticklebacks (in) rock

ResearchBlogging.orgThere are millions of sticklebacks across the globe, but you can also find sticklebacks in fossil form. The scientific name for most fossil sticklebacks is Gasterosteus doryssus, but morphologically this fossil “species” belongs within the threespine stickleback complex.

One Miocene fossil site has offered up some fascinating insights into the pace of evolution in threespine stickleback. Today I’ll be focusing on a paper that examines evolution in diet type in this unique stickleback “population”.

A few weeks ago, I mentioned “limnetic” and “benthic” stickleback – two different morphs of freshwater stickleback that live in different places within a lake and eat different things. Limnetic stickleback generally swim in the open areas of the lake and feed on zooplankton like calanoid copepods. Benthic stickleback stay close to the lakebed and feed on insect larva and small crustaceans like gammarids and ostracods.

In an earlier paper, it was shown that you can identify whether a stickleback is benthic or limnetic just from tiny scratches on the teeth. That technique was applied to fossil sticklebacks, with some striking results: at different periods in time, the population changed from limnetic to benthic and back again to limnetic.

Most stickleback in this lake were limnetic, which makes a lot of sense – in order for the stickleback to be preserved in anoxic sediment, the lake had to be fairly deep, which opens up a lot of potential habitat for limnetic stickleback. In addition, the substrate the sticklebacks are buried in is called diatomaceous earth – basically, millions and millions of dead diatoms, a type of phytoplankton. Lots of phytoplankton swimming around suggests there was zooplankton that ate them, which would provide a perfect source of food for limnetic stickleback.


Fossil sticklebacks (photo courtesy of Michael Bell)

So what about the point in time where the population changed from limnetic to benthic? The authors suggest that because of the speed of the change – and because there are few sticklebacks from these rocks that are halfway between benthic and limnetic – it might be the case that the limnetic sticklebacks went extinct and were replaced by a new population of invading benthic stickleback.

Still, even if we can’t say for sure whether the limnetics were replaced by benthics or whether they evolved into benthics, we can say that the benthic population evolved into a limnetic population over a few thousand years, because the pattern of tooth wear changes from the heavy markings typical of a benthic to the lighter markings typical of a limnetic.

It’s rare that we can use fossils to examine how a specific population changes over time, but because we can take our understanding of modern stickleback and apply it to the fossils, we can learn a lot about the dynamics of evolutionary change.

Purnell, M., Bell, M., Baines, D., Hart, P., & Travis, M. (2007). Correlated Evolution and Dietary Change in Fossil Stickleback Science, 317 (5846), 1887-1887 DOI: 10.1126/science.1147337

Stickleblog: The stickleback family tree, part 2

ResearchBlogging.orgSome weeks ago, I discussed a large phylogenetic study that separated sticklebacks from the seahorses and pipefishes – today I’m going to discuss a phylogenetics paper that zooms in on the relationships between different sticklebacks(and their very closest relatives).

Many of the same scientists from the earlier stickleback phylogeny were involved in this paper, though there is one new face, Yale’s Tom Near, a longtime Wainwright Lab collaborator and former CPB Postdoc.

The group sequenced the mitochondrial genomes of all nine sticklebacks and stickleback relatives, and they also sequenced 11 nuclear genes. They used both maximum-likelihood and Bayesian methods to estimate a phylogenetic tree of sticklebacks.

Here’s what they found:

The mitogenome and nuclear gene data dovetail beautifully, as do the maximum-likelihood and Bayesian methods for each dataset, so there’s every reason to feel confidant about this arrangement of species.

There are a number of interesting results here: Aulorhynchidae, the family that includes the tubesnout, turns out to be paraphyletic – perhaps the Aulorhynchidae should be folded into the family Gasterosteidae and considered proper sticklebacks?

The thing I find the most interesting is the phylogenetic position of Spinachia spinachia, an elongated stickleback similar in appearance to the tubesnout. The paper suggests that perhaps Spinachia‘s elongate form is the result of convergent evolution.

It’s also worth thinking about the geographical distribution of stickleback in the context of this phylogeny: Spinachia and Apeltes, two Atlantic Ocean-only species, are grouped together, while the most basal stickleback relatives are all found in the North Pacific.

There are some interesting future directions possible here as well. One of Tom’s specialties is using fossil data to calibrate phylogenies, so it’s likely we’ll see a phylogeny in the near future that gives us an idea of the timescales of major stickleback divergence events.

KAWAHARA, R., MIYA, M., MABUCHI, K., NEAR, T., & NISHIDA, M. (2009). Stickleback phylogenies resolved: Evidence from mitochondrial genomes and 11 nuclear genes Molecular Phylogenetics and Evolution, 50 (2), 401-404 DOI: 10.1016/j.ympev.2008.10.014

Stickleblog: Get ready for sticklebacks!

This is the first installment of a weekly feature on the Wainwright Lab blog.

First, a little introduction: My name is Matthew McGee, and I’m a graduate student in the Population Biology program at UC Davis with Peter Wainwright.

(For those wondering, Peter is the derived fish on the left.)

The species I’m primarily interested in is the threespine stickleback, Gasterosteus aculeatus (which I generally refer to as just “stickleback”, because they’re much more commonly used in research than the other stickleback species).

My research deals with stickleback functional trophic morphology and evolution; or put another way, how the food sticklebacks eat shapes their appearance and how they change over time.

Threespine stickleback, Gasterosteus aculeatus


(Image courtesy of Wikimedia Commons)

So why sticklebacks in particular?

Clearly, because sticklebacks are awesome.

They’re awesome because they have a few key qualities that make them an excellent model system for evolutionary biology. Sticklebacks are marine fish that can tolerate freshwater, and populations of stickleback will often colonize lakes and streams from the ocean, then diverge from the marine population in interesting ways.

From a functional perspective, they’ve got a great assortment of interesting traits: lateral “armor” plates, serrated pelvic spines instead of fins, different mouth shapes, and they produce their own form of glue!

Stickleback are also a great genetic system, because they have a fully sequenced genome, and it’s easy to cross different types of stickleback with each other, which can help us locate the genes involved in particular traits.

As if that wasn’t enough, stickleback are also a model system for behavior, toxicology, and development.

In short, sticklebacks = awesome.

Every week, I’ll be blogging on a different aspect of stickleback biology, which will usually involve a discussion of a stickleback-themed peer-reviewed research publication.

Join me next week, when I talk about phylogenetics and the stickleback family tree!

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