Showing posts with label speciation. Show all posts
Showing posts with label speciation. Show all posts

Wednesday, April 29, 2009

In Good Company

Congrats to fellow Dechroner, Luke Harmon, who along with several colleagues has a nice paper in this week's Nature. In this article, they describe their research on how the diversification of species via an adaptive radiation strongly affects the ecosystem itself, through a series of studies of sticklebacks. There's a nice News & Views on their article as well. Good work, Luke (et al.)!

Monday, April 6, 2009

Complexity in Crustaceans: A Driven Trend in Organismal Design

One of my favorite papers from last year was the analysis by Adamowicz et al (PNAS) of an apparent trend towards increasing complexity within the Crustacea. Evolutionary biologists have long been fascinated by trends, and many have at least some familiarity with Cope’s Rule, the proposed trend towards increasing body size within lineages. Adamowicz and colleagues looked at complexity within multiple lineages of crustaceans, from the Cambrian to the present. They found that many indices of complexity, including number and disparity of limb types as well as disparity of limb form, generally showed parallel increases in complexity through time.

The very issue of whether complexity is a trend has been controversial (e.g., McShea 1996). Moreover, some might complain that this smacks too much of orthogenesis or progressionism for their tastes. And what do we mean by complexity, anyway? These issues have been and will continue to be debated in the literature. But one of the neatest things about the Adamowicz paper is that they provide a possible mechanism for a trend in complexity. They found that newly originated higher taxa had greater limb differentiation than their contemporaries, and that taxa going extinct had lower degree of limb differentiation. Moreover, limb complexity turns out to be one of the strongest predictors of species richness in extant crustacean clades. Together, these suggest the possibility that the trend in complexity might be driven in part by differential speciation and extinction of lineages based on complexity. What if lineages with higher complexity diversified at greater rates than lineages with reduced complexity? Over time, traits associated with complexity might increase simply because of this connection to diversification. This research thus raises some intriguing levels of selection issues, because there is – in principle – no reason why complexity could only be favored by selection at the individual level.

How might limb complexity fuel the diversification process? The authors speculate that increased limb complexity might increase ‘evolvability’ (the meaning of which is even more fun to discuss than ‘complexity’!) and possibly promoting niche specialization. They also note that new limb types might amplify the intensity of sexual selection, possibly serving indirectly to enable that supposed ‘engine of speciation.’ Anyway, don’t expect this paper to end with a case-closed feeling – after all, questions like these are on par with the biggest unresolved issues in biology. But there are lots of things to think about here!

Sunday, March 29, 2009

Speciation with gene flow?

Liam’s post on nested clade analysis (below) reminded me of this very recent paper by Becquet and Przeworski (Evolution, online accepted). Many of us are interested in understanding whether speciation typically entails an abrupt cessation of gene flow between populations, or whether the process is “leaky”, with continued exchange of migrants after the initial population split. These are typically referred to as the “isolation” and “isolation-migration” models, and several computational tools have been developed to estimate parameters relevant to the isolation-migration model (IM, MIMAR).

Becquet and Przeworski look at both of these programs (and MIMAR is one of their own) and ask the simple question of how they perform when some of their underlying assumptions are violated. Their answer: not as well as one might like. When ancestral populations are structured, both IM and MIMAR can lead to rejections of a true allopatry (isolation only) model, even when there is no post-separation gene-flow. Moreover, parameter estimates – including divergence time and ancestral population sizes – become unreliable when there is ancestral population structure or when gene-flow rates change through time. Real population histories likely involve both time-varying levels of gene flow and complex current and historical population structure and it is not clear how to develop methods that are robust to a broad range of potential splitting scenarios. Approximate Bayesian methods, anyone?