The pink fairy
armadillo or pichiciego is the smallest
species of armadillo (mammals of the family Dasypodidae, recognized by a bony
armor shell), first described by R. Harlan in 1825. This desert-adapted animal
is endemic to central Argentina and can be found inhabiting sandy plains,
dunes, and scrubby grasslands.Pink fairy armadillos have small eyes, silky
yellowish white fur, and a flexible dorsal shell that is solely attached to its
body by a thin dorsal membrane. In addition, its spatula-shaped tail protrudes
from a vertical plate at the blunt rear of its shell.
This creature
exhibits nocturnal and solitary habits and has a diet that is mainly composed
of insects, worms, snails, and variousplant parts.Unfortunately, the
conservation status for pink fairy armadillo is still uncertain, and it is
listed as Data Deficient by the IUCN Red List of Threatened Species. The
decline in population for this species has generally been attributed to farming
activities and predators including domestic dogs and cats. Pink fairy
armadillos are found less commonly than they were a few decades ago, and the
field sightings have been rare and incidental. Individuals that have been
caught in the wild had a tendency to die during or a couple days after they
were transported from their natural habitat to captive facilities. There is a
sole record for the longevity of a pink fairy armadillo that was held in
captivity more than 4 years; however, that particular case lacks proper
scientific description and thus cannot be considered fully valid. Armadillos'
evolutionary distinctiveness, combined with their restricted geographic range,
ongoing threats, and rarity makes the urgent conservation attention extremely
important for these species.
At present,
fairy armadillos have the least molecular data available within the armadillo
family. This genus includes only 2 living species of fairy armadillo:
Chlamyphorus truncatus (pink fairy armadillo) and Chlamyphorus retusus (chacoan
orgreater fairy armadillo). These two species are morphologically similar: both
have notably reduced eyes and reinforced forearms that support enlarged digging
claws. Both species are specialized to subterranean lifestyle which was
developed in their ancestral lineage sometime between 32 and 17 Mya. Both
species have allopatric distributions; both are strictly nocturnal but the
details of their ecology and population biology remain unknown. The
similarities can be explained either by the presence of a shared common
ancestry, which would prove the monophyly of both species, or by the result of
adaptiveconvergence due to extreme selective pressures induced by their
lifestyle (which would suggest the diphyletic origin). In 2012, the first
theory has been proven. The split between these two species was estimated to
have occurred around 17 ± 3Mya, around the transition between Early and Middle
Miocene.
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