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Fig
Research
Figs (Ficus
sp., Moraceae) and their pollinating wasps (Agaonidae, Chalcidoidea,
Hymenoptera) constitute one of the most extraordinary pollination mutualisms
known. The fig depends completely on its pollinating wasp for being pollinated
and the wasps on the fig for completing its life cycle. In addition to
the pollinating wasps, a diverse community of non-pollinating wasps also
exploits figs. Individual host fig species may harbor many different
species of non-pollinating wasps, and related host figs may possess very
similar assemblages of these species. Further, species-specific parasitic
nematodes (Parasitodiplogaster sp., Diplogasteridae) associated with the
pollinating wasps are also found in the system.
We
are interested in understanding the causes of fig species diversity
The nearly 750
described species of figs (Ficus sp.) occur worldwide in tropical
and subtropical regions,
and are considered “keystone” species in tropical forests
due to their year-round production of fruit essential to a large number
of frugivores. At the phenotypic level figs are an extremely diverse group
of plants, and allozyme studies have shown that allele diversity and overall
heterozygosity in Neotropical figs (sect. Urostigma) are among the highest
reported in flowering plants. Such high genetic diversity could be simply
the result of large historical effective population sizes. However, field
observations on the figs and genetic data on the pollinators suggest a
different but not mutually exclusive explanation: it is possible that
Neotropical figs are not “good” biological species, and that
gene flow between species is prevalent and plays a fundamental role in
the generation of the tremendous diversity of what we recognize as different
fig species. That interpretation arises from the observation of several
cases of potential hybrid phenotypes in nature, the fact that pollinating
wasps occasionally enter and successfully reproduce in the “wrong”
host fig species (often resulting in viable hybrid seeds), and genetic
data we have obtained that shows that there are several cases of more
than one species of wasp pollinating the same species of fig.
To address this hypothesis we have developed a battery of sequencing markers
based on sequences from cDNA clones obtained from cDNA libraries of two
Neotropical fig species (F. citrifolia, F. popenoei) and one fig pollinator
species (Pegocapus estherae) that were constructed in our lab. 2000 clones
were sequenced and the sequences have been used to find variable markers
that are being used in population genetic studies of species divergence
in Neotropical fig species. These mini-genomic resources are being used
to collect phylogenetic and population genetic data to test the long-held
idea of strict-sense cospeciation between closely related species of figs
and their pollinators, and to test our hypothesis that gene introgression
in figs due to pollinator host switches or host sharing has been the main
mechanism involved in the generation of fig species diversity.
Our initial phylogenetic and population genetic data has been published
(Machado et al. 2005) and more data is being collected for a larger study.
In the future we want to develop additional markers using our cDNA database,
and to increase the geographic sampling of the study (currently confined
to the Panama Canal area).
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