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Because the thylacine's anatomy has been recorded nearly as well as that
of most other Australian mammals, with the possible exception of the macropodids,
it is possible to discuss its position within the Marsupialia. Among
the thylacine's advanced physical characteristics are large size, digitigrade
stance, enlarged brain, lengthened jaws and sectorial molars which in some
respects parallel those of canids and felids. These adaptations evolved
to facilitate cursorial hunting of large to medium-sized prey and represent
the end result of a very long period of evolution from a primitive marsupiocarnivore
stock.
Many earlier authorities such as Le Souef and Burrell (1926), and
Troughton (1967) usually categorized the thylacine with the Dasyuridae
partly because the dasyurids are the only carnivorous, polyprotodont, didactylous
group in Australia.
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| A
thylacine "kangaroo standing" at the Hobart Zoo (Domain site). In
the wild, thylacines use this upright posture to gain a better view of
their surroundings. Because the thylacine's heel has a long and narrow
tract of bare, roughened skin along its length, it is evident that the
animal frequently rests it on the ground in a kangaroo-like stance.
This image is from a film
taken in 1928. |
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The majority of the distinctive features of the thylacine are specializations
of characteristics present in all marsupicarnivore stocks, as well as placental
carnivores. The thylacine's limb proportions are similar to those
of the dasyurids, despite its larger size. Its reproductive system
is also quite dasyurine in form. By most counts, Thylacinus
is no further removed from the Dasyuridae than is Myrmecobius (numbat).
The thylacine was considered by Tate (1947) to be related to the Short-haired
marsupial "mice" (Murexia spp.) of New Guinea on the basis of the
progressive increase in size of the posterior molars, and the tubular braincase
with post-orbital constriction which is seen in some mature male examples
of Murexia. However, since these characteristics are virtually
the only similarities between the genera (Archer 1976c), this theory gained
little support. |
On a dental basis, the relationship becomes tenuous. The morphology
of the shearing crest differs from that of all dasyurids, and the loss
of the stylar cusps in a form with enlarged third premolars also contrasts
with the overall dasyurid trend. This suggests that the dasyurid
and thylacinid lines diverged quite early. A closer relationship
to the now extinct borhyaenids
of South America was proposed by Bensley (1903). Formerly, this view
was partly upheld by Archer (1976c). However, Archer (1976b) stated
that basicranial evidence tends to point to a didelphid rather than borhyaenid
relationship.
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By 1982, a comparative study of blood proteins called albumins had demonstrated
that the thylacine is in fact very closely related to the dasyurids, and
suggested that it had branched off from the main dasyurid line approximately
12 million years ago. A decade later, analysis
of DNA recovered from a preserved thylacine pelt provided an even stronger
confirmation of this evolutionary affinity. The borhyaenid
link was simply another deceptive case of evolutionary convergence: similar
lifestyles create similar physical forms. However, the albumin study
also misled evolutionary biologists by underestimating how long ago the
thylacinids and dasyurids had diverged from an early proto-dasyurid predecessor. |
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| A
thylacine photo taken by Harry Burrell at the Hobart Zoo (Beaumaris site)
in 1912. As was the case with the other thylacine photos from Burrell's
series (all of which were probably taken on the same day), this one was
greatly cropped before being published. Compare it with the
original
version. |
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The recent discoveries
of a number of fossil thylacinid species and at least one ancestral dasyurid
at Riversleigh
(north-western Queensland) from approximately 22 million years ago suggest
a minimum divergence time of 25 million years, and possibly even as far
back as 30 to 40 million years ago. Although
fossils of primitive marsupicarnivores have been found in the rocks of
central Australia (Archer 1976a), our understanding of the precise history
of this group remains as of yet rather incomplete.
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| Another
one of Burrell's thylacine photos (1912). This particular image is
considered by some to have played an important role in promoting the unsubstantiated
belief that the thylacine was a significant predator of poultry.
While it is true that thylacines may have occasionally been fed chickens
in zoos, there is no strong evidence that the species ever posed any serious
threat to domestic fowl, sheep or other livestock. The structure
of the thylacine's jaws and teeth appears to be much more suited to dealing
with species of wild prey such as small to medium-sized mammals.
The photo shown above is the cropped version which appeared in a 1921 issue
of
Australian Museum Magazine, as well as various other publications.
Compare it with the original. |
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The thylacine's preferred habitat and hunting technique remain under debate.
The widespread distribution of fossil T. cynocephalus material proves
that, even allowing for climatic change, the species' range of habitats
was once wide, a fact which is demonstrated by the fossils that have been
found in association with it. Similarly, the thylacine's alleged
preference for dense forest may have possibly come about as a result of
persecution by man. |
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