The Origin and Evolution of Mammals - Moodle
The Origin and Evolution of Mammals - Moodle
The Origin and Evolution of Mammals - Moodle
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the presence <strong>of</strong> a deep, longitudinal groove along<br />
the dorsal edge <strong>of</strong> the dentary, called the dentary<br />
sulcus. <strong>The</strong> posterior part <strong>of</strong> the feeding apparatus<br />
appears to have been more important than in other<br />
dicynodonts, with a slicing, knife-like blade on the<br />
lower jaw shearing against a horny palatal pad. In<br />
most members <strong>of</strong> the group, the premaxillary margin<br />
is also sharp <strong>and</strong> fits quite closely against the<br />
outer edge <strong>of</strong> the dentary, indicating a cutting<br />
edge perhaps suitable for cropping palate-sized<br />
bites <strong>of</strong> leafy vegetation, with the different species<br />
specialised for h<strong>and</strong>ling the foliage <strong>of</strong> different<br />
forms <strong>of</strong> glossopterid trees, shrubs, etc. (Cox 1998).<br />
Pristerodon is a primitive member <strong>of</strong> the group. It is<br />
small in size with a broad intertemporal ro<strong>of</strong>, <strong>and</strong> possesses<br />
small postcanine teeth in both upper <strong>and</strong> lower<br />
jaws (King <strong>and</strong> Rubidge 1993). Common <strong>and</strong> widespread<br />
in Africa, it existed from the Tapinocephalus<br />
to the Dicynodon Assemblage Zones, a longevity<br />
matched otherwise only by Diictodon (Angielczyk<br />
2001), <strong>and</strong> it also occurs in India. <strong>The</strong> adaptive<br />
radiation which occurred from a hypothetical<br />
EVOLUTION OF MAMMAL-LIKE REPTILES 49<br />
Pristerodon-like ancestor includes such familiar<br />
types as Oudenodon which lost its tusks but retained<br />
the wide intertemporal region <strong>and</strong> narrow snout.<br />
According to Hotton (1986), Oudenodon held its<br />
snout forwards when feeding, indicating that its<br />
source <strong>of</strong> food was vegetation well above ground<br />
level. This group also includes the largest <strong>of</strong> the<br />
Permian dicynodonts, with skull lengths up to 50 cm.<br />
Aulacocephalodon is a fairly large, wide-snouted<br />
pristerodontoid in which the front edge <strong>of</strong> the<br />
premaxilla formed a transverse cutting blade.<br />
In contrast, the even larger Dinanomodon possessed<br />
a narrow, pointed snout which might perhaps have<br />
adapted it to browsing on higher-level foliage.<br />
<strong>The</strong>se two inevitably have been compared to white<br />
<strong>and</strong> black rhinos, respectively.<br />
<strong>The</strong> familiar <strong>and</strong> once much overused genus<br />
Dicynodon retained a pair <strong>of</strong> tusks, evolved a<br />
narrow intertemporal region, <strong>and</strong> tended to<br />
shorten the length <strong>of</strong> the palate. Haughton <strong>and</strong><br />
Brink (1954) famously listed 111 species <strong>of</strong><br />
Dicynodon, a number whittled down by King (1988)<br />
(a) (b) (c)<br />
Dicynodon Kwazulusaurus Lystrosaurus<br />
Figure 3.14 Triassic dicynodonts. (a) Dicynodon (King 1990). (b) Kwazulusaurus shakai (Maisch 2002). (c) Lystrosaurus declivis (King 1988).<br />
(d) Skeleton <strong>of</strong> Kannemeyeria (after Pearson). (e) <strong>The</strong> shansiodontine Tetragonius njalilus (King 1988, from Cruickshank). (f) Stahleckeria<br />
(King 1990 after Camp). (g) Ischigualasto jenseni (King 1988, after Cox). Continued overleaf