Phylogeny and host relationships of the Australian gall-inducing fly Fergusonina Malloch (Diptera: Fergusoninidae)
Abstract
Fergusoninidae is a monogeneric family of mainly Australian
flies. In a unique obligate mutualism with a nematode, these
flies induce galls on plants in the family Myrtaceae, and have
been recorded on seven genera of host plants, most commonly on
the eucalypts. Most host plants are associated with multiple
species of Fergusonina, usually galling different sites on the
plant. Despite the abundance and diversity of Fergusoninidae and
its tight association with Australia’s most iconic flora, the
host specificity and coevolutionary relationships of Fergusonina
with its plant hosts have not previously been examined in depth.
I used a phylogenetic approach based on mitochondrial COI to
examine the evolutionary relationships between Fergusonina
species and their plant hosts, initially performing a Bayesian
analysis of 41 putative species on flies from Eucalyptus plant
hosts. This analysis revealed well-supported lineages of flies
characterised by larval morphology and gall type, usually from
the same plant host subgenus. The deeper phylogenetic
relationships between groups of species remained unclear, so I
performed a further analysis of an expanded dataset including
flies from four host genera, using separate and concatenated COI
and nuclear CAD sequences.
Having disparate evolutionary time scales, Fergusonina and their
hosts cannot have codiverged early in the history of Myrtaceae,
but current fly-plant host specificity suggested that there may
be cospeciation at finer taxonomic levels. A fine-scale analysis
of
vi
flies collected from a clade of ten Eucalyptus species explored
the plant-fly coevolutionary relationships in three clades of
flies from different sites of the host plant: flower buds, leaf
blades and vegetative shoot buds. The degree of host specificity
displayed by the three fly groups varied markedly, with flower
bud gallers exhibiting the most cophylogenetic history, and leaf
blade gallers the least. These results suggest that host
switching occurred often in the history of Fergusonina and
Myrtaceae.
I compared molecular, morphological and ecological criteria for
determining species limits, including a number of molecular
species delimitation models. Delimiting species using a 2%
pairwise distance was most consistent with other data such as
larval and adult morphology, host and gall site. However,
molecular methods were not adequate to clarify some ambiguous
species limits, highlighting the need to integrate multiple
criteria when identifying species in this group.
Over the course of the study, I discovered around 95 unrecorded
host plant/gall site associations, indicating that the potential
number of species in this family is very large. The definable
morphological and ecological differences among the lineages of
Fergusonina, supported by molecular evidence, argue for a
revision of the genus along these lines. The type species for
Fergusonina, collected in Sydney in 1924, is in poor condition
and is not identifiable; there are no records of its host, gall
type or larval morphology, and I could not extract and DNA from
it. A neotype will need to replace the existing holotype, or the
type species assigned to a probable group. After a comparison of
morphological characters I concluded that the type species is
likely to belong to a group associated with the host genus
Corymbia.
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