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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

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