Taxonomic status of Melaleuca argentea "Ashburton biotype" and identification and evaluation of exon capture loci for Myrtaceae
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Choi, Bokyung
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Canberra, ACT : The Australian National University
Abstract
Melaleuca sensu lato is the second biggest genus (ca. 380 spp.) that is mainly distributed in Australia, but some species are found in Southeast Asia, Papua New Guinea and New Caledonia. Melaleuca occupy a range of habitats and are found in all biomes, which makes this hyper-diverse genus an excellent group to carry out evolutionary studies.
The taxonomy of Melaleuca sensu lato (tribe Melaleuceae) has been controversial. The tribe originally included eight other genera: Beaufortia, Calothamnus, Conothamnus, Eremaea, Lamarchea, Petraeomyrtus, Phymatocarpus, and Regelia. However, with taxonomic changes all of the genera in the tribe were transferred to Melaleuca. To date, the phylogenetic studies based on molecular data have shown that Melaleuca is paraphyletic with respect to the other genera in the tribe. However, the taxonomic boundary of Melaleuca is still debated. Existing molecular phylogenies of Melelauceae have used only a few genetic markers, and the relationships within the genus remain unresolved with large polytomies.
Taxonomy of eucalypts has been problematic. Eucalypts include the
following seven genera (Eucalyptus, Corymbia, Angophora,
Arillastrum, Allosyncarpia, Stockwellia, Eucalyptosis). They are
mainly Australian but some genera/species extend outside
Australia. The taxonomic relationship of Corymbia, and Angophora
is still debated. Some molecular phylogenies have shown monophyly
of Corymbia and Angophora while Corymbia was paraphyletic with
respect to Angophora in other studies.
In Chapter 2, the genetic diversity of Melaleuca argentea (M.
leucadendra complex) was explored. Previous research suggested
that populations in the Pilbara region of Western Australia had
some genetic distinctions. The Pilbara populations were recorded
as M. argentea “Ashburton biotype” (AB) in older literature,
but no further information was available. Morphological
characters and molecular data to assess the taxonomic status of
the Pilbara population were used. We found that AB is more
similar and closely related to M. leucadendra than to M.
argentea. The results did not have conclusive evidence to support
that AB is a distinct species from M. leucadendra. In order to
test the taxonomic status, presence of gene flow between AB and
M. leucadendra need to be further tested.
With the ultimate aim of estimating a comprephensive phylogeny of
Melaleuca and eucalypts using more samples and many more loci
compared to previous studies, we developed genetic markers for
exon capture in Chapter 3. A workflow to locate orthologous and
low copy number nuclear loci is introduced along with the method
that was employed to identify the chloroplast markers. 209
chloroplast and nuclear loci that might be useful for Myrtaceae
were identified by and 43 Myrtaceae taxa were successfully
sequenced.
In Chapter 4, a gene tree approach for each individual locus was
undertaken to remove potentially paralogous loci. We have found
144 loci that might be useful for Melaleuca and 174 loci for
eucalypts. The present study contributes towards more robust
estimations of phylogenetic relationships in the genus Melaleuca,
eucalypts as well as other genera in Myrtaceae. Further work is
required to verify the markers and to study phylogenetic
relationships of the taxa at different taxonomic levels using the
loci.
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Keywords
Myrtaceae, exon capture, phylogeny, Melaleuca leucadendra complex, morphometric analysis, morphological characters, gene trees, concatenated dataset, haplotype network, loci identification, nuclear marker identification, chloroplast marker identification, genetic markers, taxonomic status, Pilbara, Melaleuca argentea "Ashburton biotype", Melaleuceae, Melaleuca sensu lato, Eucalypts, Eucalypteae, Eucalyptus
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