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Terrestrial Palaeoecology and Global Change

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

Dinosaurs, etc. Temperization leads to afforestation of mid-latitudes <strong>and</strong> a spread<br />

of deciduousness (VII.5). Since deciduous forests are inferior to open evergreen vegetation<br />

in resilience <strong>and</strong> in nutritional quality of the leaf mass, afforestation means a drastic<br />

reduction of trophic resources for the larger herbivores.<br />

Dinosaur extinction is commonly perceived as enigmatic, implying an exotic explanation.<br />

Yet dinosaurs were the larger herbivores dependent on phytomass production,<br />

<strong>and</strong> predators dependent on the herbivore biomass. The early diverging insectivorous<br />

line supposedly gave rise to the birds. The later mammalivorous branch might perish<br />

with multituberculates <strong>and</strong> other archaic mammals. In the history of dinosaurs there<br />

were at least two episodes of semiextinction at the Triassic/Jurassic boundary <strong>and</strong> in<br />

the mid-Cretaceous (the ornithopod/sauropod replacement), both related to vegetational<br />

changes.<br />

Afforestation over the KTB affected the habitats of the richest dinosaur faunas in<br />

North America, Amurl<strong>and</strong>, Mongolia, northern China <strong>and</strong> elsewhere at the mid-latitudes.<br />

The end-Permian afforestation involved the same areas, with the Eurangarian<br />

vegetation extending to northern China. On taphonomic evidence, most of the dominant<br />

arboreal forms were shoot-droppers. This kind of deciduousness primarily affects the<br />

larger browsers that prune leafy shoots at high browsing levels (VIII.I.3).<br />

The residual dinosaur communities of forested areas might have foraged on the residual<br />

patches of cycadophyte thickets (as suggested by association of dinosaur remains<br />

with Encephalartites in the Maastrichtian of Koryak Highl<strong>and</strong>s: Krassilov et al., 1990).<br />

Judged by the aquatic morphological adaptations <strong>and</strong> the gut contents, the Maastrichtian<br />

duck-bills consumed a low nutritional aquatic phytomass or gyttja (Krassilov, 1981a;<br />

Krassilov & Makulbekov, 1995).<br />

The trophic factor might have inflicted a turnover of tetrapod communities at the<br />

PTB as well. Most of the Permian terrestrial tetrapods became extinct towards the end<br />

of this period. The end-Permian to Early Triassic lystrosaurids were ecologically equivalent<br />

to the Maastrichtian hadrosaurids, both switching from browsing to aquatic grazing<br />

in response to afforestation <strong>and</strong> the growing aquatic production (eutrophication, above).<br />

Later in the history, afforestation over the shrub-tundra <strong>and</strong> savannoid “tundra-steppe”<br />

l<strong>and</strong>scapes drove to extinction the larger browsers of the Late Pleistocene mammalian<br />

faunas (Ukraintseva, 1986).<br />

Iridium. The cosmic impact model of the KTB extinction (Alvarez et al., 1980)<br />

implies a giant crater, for which the 250 km wide Chicxulub is considered as the most<br />

plausible c<strong>and</strong>idate. It is a multiring basin with a central peak ring <strong>and</strong> a prominent Moho<br />

rise beneath (Sharpton et al., 1992; Christeson et al., 2001). The latter feature seems to<br />

better agree with magmatic origins. The rock melts <strong>and</strong> brecciation by allogenic impacts<br />

(reviewed in Dressler & Reimold, 2001) are scarcely different from those caused by<br />

explosive volcanic eruptions. Whatever the origins of Chicxulub, its correlation with the<br />

KTB is unlikely because no evidence of an impact-generated (or a volcanic eruption<br />

generated, as it might be) tsunami has been found in the transboundary sequences of the

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