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Also, it provides an additional line of evidence supporting genetic and morphological data that indicate the SABD is distinct from the CBD in Victoria, Australia.
Although there is some morphological data that has been interpreted to suggest that some microsporidian species may undergo sexual reproduction [31], [32], this is not known for any of the six species in the current analysis.
These relationships were not recovered in cladistic analyses of morphological data that included representatives of a larger number of genera.
However, most of the morphological data that have been published are derived from in vitro and in vivo studies and few reports of direct evidence obtained from patient-derived samples have been described.
In Mutanen et al. [ 9] and the ML analysis based on DNA-data only of the present study (Additional file 8), the sister-group relationship between the two superfamilies was not recovered suggesting that it is the addition of morphological data that brings about this relationship in the present result.
This data provides an additional line of evidence supporting the genetic and morphological data that the SABD is distinct from the CBD in Victorian waters, Australia.
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This might be useful not only for morphological data matrices that only contain variable sites but also for alignments of SNPs.
To take advantage of currently available models of evolution an approach to morphological data collection that includes autapomorphies may be necessary to minimize the consequences of saturation in morphological data sets.
However, the same five clades that were recovered based on DNA sequence data were also recovered using a purely morphological data set that utilized numerous character states that had not previously been considered in the classification within Petrocosmea, albeit the fewer number of morphological characters did not yield the same level of support for the clades.
Indeed, our morphological data suggest that RINs initially undergo a form of somal translocation similar to that of young RGCs and photoreceptors (Randlett et al., 2011b; Suzuki et al., 2013; Zolessi et al., 2006).
These morphological data suggest that in Physcomitrella branches initiate de novo from the epidermis of the gametophore axis and that initiation is usually, but not invariably, acropetal.
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