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The Origin and Evolution of Mammals - Moodle

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Although there is no mammal-like contact between<br />

the dentary <strong>and</strong> the squamosal bone, eucynodonts<br />

do have a secondary contact between one <strong>of</strong> the<br />

postdentary bones, the surangular, <strong>and</strong> the<br />

squamosal. It lies immediately laterally to the articular–quadrate<br />

hinge <strong>and</strong> presumably functioned to<br />

stabilise the jaw articulation. <strong>The</strong> front ends <strong>of</strong> the<br />

paired dentaries have fused to form a strong,<br />

immobile symphysis. <strong>The</strong> eucynodont postcranial<br />

skeleton (Jenkins 1971b) shows a number <strong>of</strong> evolutionary<br />

modifications towards the mammalian condition,<br />

such as the appearance <strong>of</strong> a definite acromion<br />

process on the scapular for attachment <strong>of</strong> the clavicle.<br />

<strong>The</strong> ilium is more exp<strong>and</strong>ed <strong>and</strong> the pubis more<br />

reduced compared to Thrinaxodon. <strong>The</strong> head <strong>of</strong> the<br />

femur is well turned in <strong>and</strong> the major <strong>and</strong> minor<br />

trochanters are enlarged <strong>and</strong> very mammalian in<br />

form. In the early eucynodonts from the Cynognathus<br />

Assemblage Zone <strong>of</strong> South Africa, such as<br />

Diademodon <strong>and</strong> Cynognathus, the costal plates on the<br />

ribs are still well developed, but by the Middle<br />

(a)<br />

Cynognathus<br />

EVOLUTION OF MAMMAL-LIKE REPTILES 65<br />

Triassic they are either greatly reduced, as in certain<br />

traversodontids, or completely absent, assumed to<br />

have been secondarily lost, as in probainognathians.<br />

While there are several non-mammalian eucynodont<br />

taxa that are well categorised <strong>and</strong> more or less<br />

universally accepted, the interrelationships among<br />

them remains a matter <strong>of</strong> controversy, <strong>and</strong> at least<br />

three recent cladistic analyses have produced results<br />

at variance with one another. Pr<strong>of</strong>oundly embedded<br />

in this taxonomic disagreement is disagreement<br />

about exactly which <strong>of</strong> the non-mammalian cynodonts<br />

is the most closely related to Mammalia, an<br />

issue taken up later in the section. <strong>The</strong> more or less<br />

unchallenged monophyletic subgroups <strong>of</strong> eucynodonts<br />

are these.<br />

● Cynognathidae: a family <strong>of</strong> relatively primitive<br />

carnivores<br />

● Diademodontoidea: two families <strong>of</strong> herbivorous<br />

eucynodonts, Diademodontidae <strong>and</strong> Traversodontidae<br />

(b)<br />

cor.pr.<br />

cor.pr.<br />

ang.pr.<br />

ART<br />

refl.lam.<br />

ART<br />

refl.lam.<br />

Figure 3.21 (left) (a) Skull <strong>of</strong> Cynognathus in four views. Approx. skull length 29 cm (Broili <strong>and</strong> Schröder 1934). (b) Medial <strong>and</strong> lateral views <strong>of</strong><br />

lower jaw (Kermack et al. 1973). (right) Probainognathian cynodonts. (b) Skull <strong>of</strong> Lumkuia fuzzi in four views. Skull length approx. 6 cm (Hopson<br />

<strong>and</strong> Kitching 2001) (c) Skull <strong>of</strong> Probainognathus jenseni in four views (Carroll 1988, from Romer 1970). (d) Chiniquodon (Probelesodon). Skull length<br />

approx. 11 cm ( Romer 1969). (e) Lateral view <strong>of</strong> skull <strong>of</strong> Ecteninion lunensis. Skull length approx. 12 cm (Martinez et al. 1996). ART, articular.<br />

ang.pr, angular process. cor.pr, coronoid process. refl.lam, reflected lamina <strong>of</strong> the angular. Continued overleaf

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