I doubt that they think that. Especially as the extinct armadillo genus
Macroeuphractus was heterodont. Also, what homodont sloths? (So far all
the sloths I've found details on have caniniform and molariform teeth.)
On a broad scale, and considering a single trait, heterodonty and
homodonty are equally parsimonious as the ancestral state in Xenartha:
heterodonty requires a transition to homodonty in Cingulata and
Vermilingua, and homodonty requires a transition to homodonty in
Xenartha (heterodonty goes way back in mammalian ancestry: a short
browse up the phylogenetic tree at WikiPedia suggests that it's an
apomorphy of Theriodonta) and a reversion to heterodonty in Folivora.
Macroeuphractus has derived heterodonty either way.
In the absence of any stem-Xenarthrans (at least Google isn't finding
any for me) we're stuck we examining tooth development and anatomy to
resolve the issue. On the one hand the Tetrapod Zoology blog writes
"some evidence suggests that the upper caniniform in Choloepus is a true
canine". On the other hand Xenarthra as a whole has a number of derived
dental characters (e.g. monophyodonty versus diphyodonty) so one is led
to a suspicion of a restructuring on dental anatomy on the Xenarthran
stem, with homodonty as part of the suite. On the gripping hand a paper
in Scientific Reports (
https://www.nature.com/articles/srep27763 - not
paywalled) says that Bradypus has vestigal incisors as juveniles, from
which one infers that Xenarthrans had heterodont ancestors.
[There may be a usage question with regards to whether adult sloths are
heterodont - if the caniniform teeth are modified molars than under at
least some usages sloths are still homodont.]
I expect that mammalian palaeontologists and neontologists think that
dental anatomy is under the control of multiple genes, and the degree of
differentiation of teeth can change of time.
>
> And then another gene evolved in later whales to prevent heterodont dentition too? Do they think it happened individually in whales or from a common ancestor? And why would it require any more than one ghost lineage for whales?
You seem to be postulating a model of evolution in which transitions
only occur from an unspecialised homodont dentition to a specialised
heterodont dentition. That's not a problem considering Xenartha in
isolation. But if you assume that whales are primitively homodont (and
that all their ancestors were) you require the independent development
of heterodonty in Mysticeti, in various stem-Cetacean groups, in
Hippopotamidae/Anthracotheridae, in Ruminantia, in Suina, in Tylopoda,
in Perissodactyla and Carnivora (or Pegasoferae), in Meridioungulata, in
Lipotyphla, in Euarchontoglires, in Afrotheria, and so one down the
mammalian stem, with the existence of undiscovered homodont stem-taxa
for all these groups (ghost lineages). This is massively unparsimonious.
It's easier to lose a complex trait (such as the archetypal mammalian
heterodonty with distinct incisors, canines, premolars and molars) than
to evolve it. If a species adopts a lifestyle that isn't benefited by
the possession of differentiated teeth it will tend to lose the
differentiation (quickly through selection, or slowly through drift,
depending on whether they're an active handicap); if a species adopts a
lifestyle that isn't benefited by the possession of teeth it will
similarly tend to lose or simplify them.
As I understand an array of conical teeth is advantageous for catching
fish, and so animals that specialise in fish-eating will tend towards
homodonty.
Similarly animals whose prey doesn't require mastication will tend to
lose or simplify teeth. Thus this is part of the suite of characters
independently developed by anteaters (anteaters sensu strictu,
pangolins, aardvarks, numbats, echidnas). Similarly the suction-feeding,
squid-eating beaked whales have reduced dentitions.
>
> Thanks.
>
--
alias Ernest Major