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Terrestrial Palaeoecology and Global Change

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

Sedimentary basins involved in orogenic uplift <strong>and</strong> subsequent denudation, might leave<br />

no traces other than redeposited palynomorphs (e.g., the reworked Carboniferous palynomorphs<br />

in the areas devoid of Carboniferous deposists: Guy-Ohlson et al., 1987).<br />

Likewise, redeposited palynomorphs provide a timing of orogenic uplift of the source<br />

areas (e.g., of the Rocky Mountains exhumation from under the Palaeogene peneplain,<br />

with the reworked palynomorphs reaching to the Gulf of Mexico).<br />

A chronology of orogenic uplifts can also be deduced from the dynamics of altitudinal<br />

vegetation belts (Axelrod, 1965, 1997) <strong>and</strong> a spread of xeromorphic vegetation in the<br />

rain shadows, as over the piedmonts of incipient Rocky Mountains in the Late Eocene<br />

(Axelrod & Raven, 1985).<br />

Thus, both latitudinal <strong>and</strong> altitudinal differentiation of fossil plant assemblages provide<br />

evidence of tectonic reconstructions. <strong>Global</strong>ly, the vegetational zonation reflects a heat transfer<br />

controlled by geography in turn controlled by tectonics. Mountain ranges form boundaries<br />

of vegetation types, as in the case of the broadleaved/pine forest types divided by the Urals.<br />

Similarly, the Angarian <strong>and</strong> Cathaysian taphofloras in Primorye <strong>and</strong> Japan were separated by<br />

the Vladivostok – Abo system of volcanic ranges (Krassilov, 1972a). As the relationships of<br />

the Laurasian <strong>and</strong> Gondwanic floras suggest, orographic barriers for floristic exchange over<br />

the Tethys belt might have been more efficient than marine barriers.<br />

Tectonic developments also indirectly affect phytogeography by their impact on climate.<br />

Thus, a distinctness of zonal vegetation boundaries increases with a restriction of<br />

the meridional heat transfer by latitudinal mountain ranges. Sea-floor uplifts might have<br />

a similar effect by restricting deep-water circulation inflicting a monsoon depression <strong>and</strong><br />

xeromorphism of equatorial vegetation. Conversely, a spread of equatorial rainforests is<br />

owing to summer monsoons that are sustained by the tropical upwellings of psychrospheric<br />

oceanic circulation in turn related to a subsidence of l<strong>and</strong> barriers <strong>and</strong> a free<br />

passage of deep water through marine gateways.<br />

V.9.1. Tectonics <strong>and</strong> vegetation of continental margins<br />

A tectonic zonation of active continental margins with the coastal volcanic ranges,<br />

their foredeeps, isl<strong>and</strong> arcs <strong>and</strong> forearc basins is reflected in the pattern of vegetation<br />

zones <strong>and</strong> taphonomic environments. <strong>Change</strong>s of the latter are evidence of tectonic<br />

restructuring. In the Sea of Japan example (Krassilov, 1975b), differentiation of plant<br />

communities reflects both the scale <strong>and</strong> timing of tectonic events.<br />

A vegetational zonation over Japan Isl<strong>and</strong>s (Kimura, 2000 <strong>and</strong> previous work) is traceable<br />

to the maritime area of Primorye (Krassilov, 1967a). About one third of Neocomian<br />

species are distinctive for the inner (Tetori) zone of Japan as compared with the roughly<br />

contemporaneous outer (Rioseki) zone. On account of bennettite diversities, including several<br />

Dictyozamites morphotypes, the Tetori flora appears more thermophilic of the two.<br />

Since their dividing “median line” is a shear fault zone, the vegetational differences might

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