The Cichlid fish of Lake Malawi provide a laboratory for evolutionary biologists to study the processes responsible for the origin of new species. You have seen some of the elements of this species rich system that make it so interesting to scientists on my Evolution of Malawi Cichlids page, but how can we exploit this system to learn more about the processes of evolution? I am working on a number of projects focused on the Metriaclima zebra species complex of Lake Malawi in an attempt to discover the mechanisms that have resulted in their diversification. The origin of new species occurs as populations of the same species diverge along their own evolutionary trajectories. So a great way to study speciation is to study sibling species or populations of the same species to discover the forces acting to push them on their own evolutionary paths. Below I will briefly describe a few of the major things that I am working on to try to infer the evolutionary processes acting on this species complex.
Male reproductive coloration in
the M. zebra species complex: convergence or vicarience?
Throughout Lake Malawi, several distinct populations
of the typical M. zebra occur. These populations of fish are
essentially identical, except for a single feature of male reproductive
coloration. All males of some of these populations possess a blue
dorsal fin, while all males of other populations possess a red dorsal fin.
Often a blue population will be within less than a kilometer from a red
population. This distribution presents an interesting question --
are populations that are geographically proximate more closely related
to each other than distant populations, despite coloration? Or, are
all red dorsal populations more closely related to each other than they
are to their blue dorsal fin bearing counter parts? This question
has more significance than it may seem at first. These two color
morphs are ecological analogs. They apparently occupy the same ecological
niche. The fact that they never occur at the same locality is testament
to this assertion. If they are merely lake wide colonists of two
lineages that diverged early on (i.e.., before the last low water stand)
then why do they both still exist, and why in such close proximity to each
other? Is their distribution evidence that the divergence between
red and blue forms has occurred several times within the lake, possibly
with the aid of reproductive character displacement? The answers
to these questions have critical implications in both the timing and the
mechanism of speciation in Lake Malawi. If geographically proximate
populations are genetically closest (convergence),
the divergence (or speciation) of the groups would have to have occurred
since the last low water -- less than 40,000 years ago. This rate
of speciation is exceedingly fast! Similarly, if these populations
have diverged in situ, there may be merit to the idea of sympatric
speciation, or even speciation by sexual selection. Alternatively,
if red and blue populations are found to form two distinct clades (vicarience),
slightly slower rates of diversification and standard allopatric divergence
become more logical. I am examining these relationships using several
microsatellite DNA markers and calculations of genetic distance between
populations.
A phylogeny for the zebras
Because of their extremely recent origin, the species
of the M. zebra complex have been resistant to phylogenetic analyses.
As ecological analogs, they are morphologically identical. While
they differ in color, we know that color patterns are frequently convergent
(as species of divergent genera often display very similar color patterns).
Attempts at phylogenetic analysis using mitochondrial DNA sequences have
failed as a result of incomplete lineage sorting -- a effect of the
extremely young age of this group. In the absence of a phylogeny,
we have no way of making sister group comparisons which are critical to
the evaluation of the speciation process. We aim to reconstruct the
phylogeny of this group using microsatellite DNA. Microsatellites
have generally been thought to be of no utility in interspecific comparisons.
Again, because of the recent origin of this group, we believe that microsatellites
will be of use in erecting a phylogeny for this group. Initial results
indicate that microsatellites may be of use in this pursuit.
Field work in Lake Malawi
In October of 1998 I spent a month on Lake Malawi with
my advisor, Dr. Irv Kornfield. We spent much time observing the behavior
of Cichlids in their natural habitat and the phenotypic variation within
and between populations. We also collected many fin clips for genetic
analyses at home. Field work was conducted with the assistance of
Ad
Konings, Martin Geerts, and
Stuart
Grantof Salima, Malawi. Below are some pictures of Lake Malawi.
Pictures Coming Soon....
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This work on Malawi Cichlid fishes is supported by
the National Science Foundation
NSF DEB 9707532