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Terrestrial Palaeoecology and Global Change

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302 Valentin A. Krassilov. <strong>Terrestrial</strong> <strong>Palaeoecology</strong><br />

a<br />

b<br />

d<br />

c<br />

Fig. 122. Extension of lacustrine rift deposits with Lycoptera–<br />

Ephemeropsis–proangiosperm assemblages (of the type shown in Fig.<br />

118) to northeastern China: (a) a fern-marsh palaeosol with Coniopteris<br />

in tuffaceous deposits of Didao Formation representing a wetl<strong>and</strong> type<br />

that became rare after the transboundary Jurassic/Cretaceous volcanic<br />

phase (b) a fish bed of Yixian Formation, a mass mortality case, (c)<br />

Gurvanella, a fruit-like proangiosperm cupule common in the Yixian<br />

Formation, (d) the same species from contemporaneous deposits of<br />

Gurvan Eren, Mongolia (Krassilov, 1982).<br />

catastrophes possibly related to volcanism <strong>and</strong> acid rains as well as an enhanced chemical<br />

weathering of the granite bedrock, a massive source of Al <strong>and</strong> F in the drainage<br />

runoff. The same factors might have been responsible for vegetation turnovers in the<br />

adjacent wetl<strong>and</strong>s.<br />

Thus, the Jurassic to Cretaceous riftogenesis <strong>and</strong> basaltic volcanism over the trans-<br />

Asiatic Mongolo-Okhotskian zone (V.5.2) provided an ecological situation for a highrate<br />

macrevolutionary development. Remarkably, a comparable proangiosperm development<br />

took place over the contemporaneous Brazilian basaltic province (Mohr & Friis,<br />

2000). Rift valleys (Fig. 125) are hot spots of basic diversification not only for higher

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