Showing posts with label ecology. Show all posts
Showing posts with label ecology. Show all posts

Monday, October 20, 2008

Phylogeny, evolution, biodiversity and ecology

ResearchBlogging.org

We are in the midst of massive upheaval in the world’s ecosystems, driven by species invasions and the sixth mass extinction in Earth’s history. How will these changes in biodiversity affect the functions of ecological communities? Will the functions of ecological systems that humans rely on for survival, such as production of oxygen, be impacted by all this upheaval?

Answering these questions requires that biologists have a good metric for biodiversity. New research by Marc Cadotte, Brad Cardinale and I, and published this week in Proceedings of the National Academy of Sciences, indicates that one particular metric of biodiversity - evolutionary diversity - is a particularly strong predictor of the biomass produced in plant communities: The more biodiversity present (measured as evolutionary diversity), the more productive the community. In fact, for the datasets we examined, evolutionary diversity was a better predictor of productivity than raw species number or number of functional groups in the community. This suggests that the most evolutionarily diverse communities may function best, and that the most evolutionarily distinct species might be the best targets of conservation efforts aimed at maximizing ecosystem productivity.

Measuring Biodiversity
One common theme in current ecological research is to ask questions about how changes in biodiversity impact or influence ecological systems or communities. This has obvious importance when we know that many species are going extinct, and that many species are being shipped around the world by human transportation. Often in ecological research, a measure of biodiversity is placed on the X-axis, and some predicted response is placed on the Y-axis, to test if there is a strong relationship. For example, one might predict that less diverse and simpler communities are more susceptible to invasive species compared to more diverse and complex communities. One might also predict that more ecological diversity leads to a healthier ecosystem, as measured by higher production. Namely, a higher diversity of organisms could make more efficient or more complete use of available resources, ultimately leading to a healthier, better functioning ecosystem.

These types of ecological studies usually use a measure of biodiversity referred to as “species richness” as the X-axis variable. “Species richness” is simply a count of the number of species. However, simply counting species makes the assumption that, say, two very closely related grass species contribute the same amount to the diversity measure as two much more distantly related species, such as a grass and a magnolia. In contrast to this implicit assumption of “species richness”, phylogeneticists often think of biodiversity in terms of evolutionary relationships, assuming that differences between species (one way to conceive of diversity) accumulate over the time since they last shared a common ancestor. To a phylogeneticist then, species that share a very recent common ancestor – like the two similar grasses mentioned above – should be nearly identical and therefore represent less total diversity compared to the much more distantly related grass and magnolia species.

We wondered if evolutionary diversity really does matter for predicting how much biomass a community produces, one measure of the health of ecological communities. Decades of experiments have already established that species number (“species richness”) is in fact correlated with productivity – the more species of plants growing together, the more biomass is produced. We extended these studies, weighing different species by how closely related they are evolutionarily. Could we better predict biomass production by also accounting for evolutionary (phylogenetic) diversity? Based on our analyses, the answer was a clear “yes”. Incorporating evolutionary distances into our biodiversity metric resulted in better predictive power of the productiveness of experimental plant communities. The metric including evolutionary history was better than “species richness” and better than the number of functional plant groups, two commonly used metrics of biodiversity.

Our data set was a collection of 40 different previously published experimental studies, conducted around the world using a total of 177 different species of flowering plants. Researchers planted experimental ecological communities, using many different combinations of plant species, and using different numbers of species. Then they let the communities grow, and measured the biomass produced by the different combinations. We added an analysis of the phylogenetic relationships of the plants using publicly available genetic data from four different genes commonly used in other studies of plant phylogeny.

Phylogenetics and Nihilism

Do all ecologists now need to become phylogeneticists? This question is similar to one asked of comparative biologists in the mid 1980’s.

In 1985, Joe Felsenstein wrote a landmark paper introducing the method of phylogenetic independent contrasts, which is now standard in comparative biology. The core message is that we cannot treat species as independent entities because they share a nested set of common ancestors. In other words, species are similar because of descent, not only because of adaptations, and traits might be correlated across species because of shared evolutionary history. At that time, comparative biologists were told they must consider phylogeny when testing for correlations among traits. Felsenstein addressed the question, “What if we do not take phylogeny into consideration [in comparative biology]?” His answer:

“Some reviewers of this paper felt that the message was “rather nihilistic,” and suggested that it would be much improved if I could present a simple and robust method that obviated the need to have an accurate knowledge of the phylogeny. I entirely sympathize, but do not have a method that solves the problem…. Comparative biologists may understandably feel frustrated upon being told that they need to know the phylogenies of their groups in detail, when this is not something that they had much interest in knowing. Nevertheless, efforts to cope with the effects of the phylogeny will have to be made. Phylogenies are fundamental to comparative biology; there is no doing it without taking them into account.”
-Felsenstein (1985)

Although other systems and other questions might differ from our study in how diversity relates to ecological processes, it seems to me that counting species is far too simplistic of a metric of biodiversity. If adding phylogenetic information was valuable in one case, it seems worthy of strong consideration any time a metric of diversity is below the X-axis in a graph. To paraphrase Joe, ecologists may understandably feel frustrated upon being told that they need to know the phylogenies of their groups in detail, when this is not something that they had much interest in knowing. Nevertheless, the evolutionary history of their focal communities or systems will often have a lot to tell them. Species are not independent entities, and biodiversity cannot be measured as if they were.

M. W. Cadotte, B. J. Cardinale, T. H. Oakley (2008). Evolutionary history and the effect of biodiversity on plant productivity Proceedings of the National Academy of Sciences, 105 (44), 17012-17017 DOI: 10.1073/pnas.0805962105

Tuesday, October 7, 2008

Fallen Giants



In the 1880's loggers felled many ancient and giant sequoia trees in an area that is now in King's Canyon National Park. The wood from these majestic trees is brittle, and mostly wasted when the trees would shatter upon impacting the ground. The 50% or so of the timber that did make it to the mills was probably used for shingles, fence posts, or matchsticks. High tannin levels make sequoia wood resistant to decay, so remnants of the fallen giants remain to this day. I visited Big Stump Grove on Saturday while clouds shrouded the tops of the living trees and drips of rain fell from the skies. Giant blackened stumps were like ghosts and piles of sawdust like blood stains.





(These pictures were snapped from my little Mino Flip Video camera because I forgot to take my still camera. I like this little video camera more and more, the more I use it.)

Wednesday, August 6, 2008

Evolve: Guts

Many evolution buffs, like myself, have been watching the History Channel Series called Evolve, which are airing here in CA at 10pm on Tuesdays. These are well produced pieces that focus each week on a particular trait (eyes last week, guts this week). Both shows have been collections of ~5 narratives, mostly showing how the focal trait works in different animals. The narratives are tied together by asserting that evolution occurred (which I am quite certain it did). As such, these are not really about the historical science of evolution, but rather they are using evolution as an organizing principle to tie together experimental science on how particular traits work in different animal groups, with a preference for charismatic vertebrates. In the end, it all works quite well, and I would recommend the series.


In honor of Guts, I thought I would post a link to some of my favorite gut science. Work by Dirk Haller and (separately) Ruth Ley lies at the interface of ecology, evolution, and medicine. They wonder, how does the composition of bacteria in the gut of humans and mice affect the host - and how does that composition of bacteria get established?

You can think of the bacteria as a community, like a forest or grassland ecosystem, living inside each of us. Communities can have different levels of diversity - they can be comprised of many of just a few species. Those species could be closely or distantly related evolutionarily. And those communities could be established from environmental sources, or established by inheritance.

I saw Dirk and Ruth talk about some of this work at last years GAFOS conference, which is a conference of about 20 Americans and 20 Germans, under the age of 40, who were invited because someone took notice of his or her work. GAFOS is funded by the National Academy of Sciences and the von Humboldt Foundation. I described it in a bit more detail in a previous post, where I linked a symposium this year on the evolution of complex adaptations.

Some of the conclusions that Ruth and her colleagues have made are that certain groups of bacteria are associated with obesity of the host. There exists an experimentally generated line of sterile mice - mice that are born and live in sterile conditions, ie with no bacteria anywhere (amazing!). Some of these sterile and genetically identical mice were seeded with different bacteria, and some combinations were more likely to result in obesity of the mice, given the same amount of food.

Another interesting result is that gut bacteria tend to be passed from mother to offspring, as opposed to being obtained from the environment. This result is based on phylogenetic trees of gut bacteria from different populations. It is heritage, not locality that determines the bulk of gut bacteria.

Dirk's presentation was a really great example of pluralism, which I like to promote. He contrasted the germ theory of disease with the genetic/inherited theory of disease. He hints at a possible link between our currently germ-o-phobic society and the increase of genetic, especially auto-immune diseases like Crohn's disease and asthma. It may be that without the insult of germs, our bodies find it more difficult to distinguish self from non-self. By just having a germ theory of disease, we lose the full picture.

(These are my memories from over a year ago, so I may have some details wrong. Check out Ruth's and Dirk's presentations on this site, to see for yourselves!)


Next week Evolve, Jaws!