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Terrestrial Palaeoecology and Global Change

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Chapter 7. Climate change<br />

193<br />

high latitudes with expansion of redbeds (as over the Permian/Triassic boundary or in the<br />

Late Cretaceous: IV.3.1). An intermittent low-latitude paralic coal zone intervening the<br />

redbed realm, as in the terminal Cretaceous (IV.3.5), is evidence of a radical global<br />

climate change.<br />

VII.1.2. Isotope ratios<br />

Isotopic compositions of carbon <strong>and</strong> oxygen, expressed as proportions of the heavier<br />

species, δ 13 C, δ 18 O, are interrelated, reflecting productivity <strong>and</strong> the dead mass export<br />

from terrestrial <strong>and</strong> marine ecosystems, the variables that fall under climatic control.<br />

Their relation to climate is mediated by the influence of temperature <strong>and</strong> precipitation on<br />

photosynthesis, biomass growth rates, continental runoff, organic <strong>and</strong> carbonate deposition,<br />

calcification of rhizolites <strong>and</strong> skeletal structures, etc. Oxygen isotope ratios of carbonate<br />

skeletons fluctuate with water temperature <strong>and</strong> salinity. The carbonate δ 18 O<br />

tends to decrease with deglaciation <strong>and</strong> the influx of meltwater, hence a correlation with<br />

deep water (in particular, NADW) production <strong>and</strong> the Heinrich events (e.g., in the Younger<br />

Dryas: Smith et al., 1997).<br />

<strong>Terrestrial</strong> biomass preferentially contributes the heavier oxygen <strong>and</strong> consumes the<br />

lighter carbon, thereby inflicting a parallel evolution of δ 18 O <strong>and</strong> δ 13 C. The lighter carbon<br />

is locked in the st<strong>and</strong>ing crop biomass, humus <strong>and</strong> the buried dead mass of organic-rich<br />

deposits. It is returned to the atmosphere with plant/soil respiration, biomass burning, <strong>and</strong><br />

the outgassing of buried organic matter. The ratios of terrestrial to marine production are<br />

reflected in δ 13 C fluctuations owing to their different 12 C consumption rates (Jasper &<br />

Gagosian., 1989). Their relative contributions depend, among other factors, on sea-level<br />

fluctuations that are in these way reflected in the δ 13 C records.<br />

Anaerobic metabolism of methane-consuming Archaea is an additional sink for the<br />

lighter isotope potentially leaving a signature in the δ 13 C records (Kuypers et al., 2001;<br />

Orphan et al., 2001). However, a recent tendency to ascribe all isotopic anomalies to this<br />

factor (e.g., Prokoph et al., 2001) does not seem warranted by the evidence, because a<br />

much higher 13 C/ 12 C ratio has been found in other chemoautotrophic organisms of the<br />

anaerobic ecosystems (Orphan et al., 2001) <strong>and</strong> the net effect might have been not so<br />

prominent.<br />

Since the globally recognized level about 7.3 Ma, but probably even earlier, the δ 13 C<br />

is also affected by the changing ratio of C 3<br />

:C 4<br />

photosynthesis that depends on the atmospheric<br />

CO 2<br />

concentration <strong>and</strong> climate.<br />

In the shallow-water carbonate precipitation systems, isotope fractionation is in equilibrium<br />

with that of the organic carbon reservoir. A correlation with terrestrial productivity<br />

is confirmed by δ 13 C carb<br />

fluctuations with precession cycles (their induced precipitation<br />

cycles) <strong>and</strong>, on a minor scale, with the monsoon index – rainforest production during<br />

the El Niño cycles (Siegenthaler, 1990; Siegenthaler & Sermiento, 1993).

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