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Reconstructing Pleistocene Climatic Change from the Oxygen Isotope Composition of Sediments: A Review

Published online by Cambridge University Press:  20 January 2017

Curt Covey*
Affiliation:
National Center for Atmospheric Research, P.O. Box 3000, Boulder, Colorado 80307, U.S.A.
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Abstract

The isotope composition of ocean sediments is the chief data source for Pleistocene climatic changes. It is generally believed that the 18O/16O ratio of a sample indicates the global total of glacial ice at the time the sample was deposited. This is roughly correct, but numerous complicating factors limit the accuracy of the isotope proxies.

Information

Type
Research Article
Copyright
Copyright © International Glaciological Society 1984
Figure 0

Fig. 1 Oxygen-isotope composition of ocean-floor sediment samples vs age of samples. Note that time increases to the left and 18O content increases downward; thus lower ice volume and warmer climates are indicated by δ180 values near the top of the graph. Solid line indicates data of Hays and others (1976), dashed line, those of Emiliani (1978). Despite their independent compilations, the two data sets are remarkably similar.

Figure 1

Fig. 2 Main features of model for predicting isotopic composition of precipitation. The model is based on concepts discussed by Dansgaard (1964). A parcel of air and water vapor is formed by evaporation from the ocean at temperature T START, raised adiabatically to pressure P*, then cooled Isobarically by an amount ΔT. Upon encountering elevated terrain (e.g. a continental ice sheet) the parcel is raised to a distance equal to the height of the ice sheet at the point of precipitation ⋄h. The 160/180 ratios in the parcel and in precipitation from the parcel are followed throughout this process.

Figure 2

Fig. 3 Isotopic composition of precipitation onto a continental ice sheet as a function of the height of the ice. Results are shown for seven model runs. “Standard” case uses values based on trajectory calculations for contemporary storms: TSTART = 10 C, P* = 75 kPa, ΔT = 5 C, and an 8‰ enhancement of isotopic fractionation due to kinetic effects during the initial evaporation. Additional curves are for changes in parameter values from the “standard” set, as described in the figure: the curves above the “standard” result from decreasing ΔT, increasing TSTART, and Increasing P*; those below the “standard” result from changes of the opposite sign. The lowest two curves show that raising the parcel further (lowering P* by 10 kPa) can have the same effect as lowering the surface temperature at which precipitation occurs (increasing ΔT by 5 C).

Figure 3

Fig. 4 Flow of Isotopes through a growing ice sheet initialized at zero at time = 0. Details of the calculation are given in Covey and Schneider (in press).