Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-22T14:57:42.987Z Has data issue: false hasContentIssue false

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.
Rights & Permissions [Opens in a new window]

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.

Type
Research Article
Copyright
Copyright © International Glaciological Society 1984

Oxygen isotopes in ocean sediments provide a continuous record of climate changes over the past several hundred thousand years (see, for example, Reference Hays, Imbrie and ShackletonHays and others (1976) or Reference EmilianiEmiliani (1978). The ratio of 180 to 160 is measured in the calcium carbonate shells of small marine fossils and the isotope composition is expressed at i180, the deviation in parts per thousand of the isotope ratio of the sample compared with the isotope ratio of a convenient standard. For the most part, the δ180 record is similar in ocean sediment cores recovered from different parts of the world (Fig.1). It is generally believed that this record reflects the global total of glacial ice; 160 is preferentially deposited onto ice sheets so that higher values of δ180 in the ocean sediments indicate higher ice volume. In the following discussion we evaluate this interpretation and conclude that it is correct to “first order”, but that (1) effects other than ice volume may control part of the amplitude of the δ180 signal, and (2) even considering the effect of volume alone, the time record of the δl80 signal is probably distorted compared with the true ice volume record.

Originally it was believed that δ18O measures the temperature of the water in which the calcium carbonate shells were formed. An increase of roughly 0.2‰ takes place for each 1 K decrease in temperature (Reference Epstein, Buchsbaum, Lowenstam and UreyEpstein and others 1953). Note that this effect operates in the same “direction” as the effect of ice volume, so that colder climates mean higher δ180. The observed increase in δ180 between today’s conditions and those of a glacial maximum is in the range from 1.5 to 2.0‰ for the fossils of bottom-dwelling as well as surface–dwelling organisms (Reference ShackletonShackleton 1967). The inferred temperature change, over 7 K, is far too large for bottom waters and thus the temperature effect cannot be the prime contributor to δ180 variations, at least in bottom-dwelling organisms.

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 Reference Hays, Imbrie and ShackletonHays and others (1976), dashed line, those of Reference EmilianiEmiliani (1978). Despite their independent compilations, the two data sets are remarkably similar.

Fig. 2 Main features of model for predicting isotopic composition of precipitation. The model is based on concepts discussed by Reference DansgaardDansgaard (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.

The ice volume effect can account for most of the amplitude of δ18O variations provided that there is enough isotopic fractionation between ocean water and glacial ice. From measurements of the isotopic composition of rain and snow at the present time and of ice from Greenland and Antarctica, it has been inferred that the great Pleistocene ice sheets were from about 30 to 40‰ lighter than ocean water (Reference OlaussonOlausson 1965, Reference Dansgaard and TauberDansgaard and Tauber 1969). Since the fraction of ocean water stored in the Pleistocene ice sheets was about 0.03, the ice volume effect would then account for a change of from roughly 0.9 to 1.2‰, or about two-thirds of the observed variation.

We have recently obtained results from a model of isotopic fractionation in evaporation and precipitation (Fig.2) which support this conclusion (Covey and HaagensonFootnote *). Results of the model depend strongly on (a) the degree to which non-equilibrium processes act in evaporation, (b) the height to which saturated air is raised after its formation, and (c) the temperature at which precipitation is formed. After obtaining representative values for these parameters by calibrating the model against isotope data from the present, we extend the calculations to predict the isotopic composition of precipitation onto the Laurentide ice sheet during the last glacial maximum. Our results (Fig.3) imply that near the ice divide, δ180 relative to ocean water should have been ~ 30‰. Since most of the ice in an equilibrium ice sheet originates near the ice divide, the conclusion is that the isotopic fractionation/ice volume effect is large enough to account for most of the δ180 signal in oceanic sediments.

It should be noted, however, that the sensitivity of isotope composition to the meteorological details of evaporation and precipitation does introduce significant uncertainties into the interpretation of a related paleoclimate proxy, namely the isotope composition of ice cores from the Greenland and Antarctic ice sheets. The amount of 180 in ice is found to decrease during glacial periods; this has been interpreted as indicating colder temperatures at the 1ce sheet surface during these times (Reference Dansgaard, Johnsen, Clausen, Langway and TurekianDansgaard and others 1971). Our results (Fig.3) show that a lowering of δ180 may indeed be caused by a decrease in temperature, but it may also be caused by a shift in precipitation patterns, e.g. by Increased uplift of precipitating air masses independent of terrain elevation. Thus the ice-core data are more ambiguous than has been hitherto appreciated.

It is important to assess the ice volume effects of the Antarctic as well as the Pleistocene ice sheets. During a glacial maximum the exposure of the Antarctic continental shelf would allow the ice sheet to expand. An approximate 10% increase in ice volume results from a shelf exposure of 0.5° latitude. The change in volume is much less than the volume of the Pleistocene ice sheets though its effect on the δ180 record would be magnified by the fact that Antarctic ice is isotopically very light.

In addition to the temperature and ice volume effects, many other factors such as variations of isotope composition within the oceans, non-equilibrium incorporation of oxygen isotopes into marine animal shells, and preferential dissolution of isotopically lighter shells can influence the δ180 signal. Reference Berger and GardnerBerger and Gardner (1975) estimate that each of these effects could contribute up to 0.5‰. Surprisingly few laboratory studies have been performed on cultured foraminifera to quantify effects such as these (Reference Erez and LuzErez and Luz 1982).

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).

Other effects may distort the time series of δ180 obtained from sediment cores away from the true ice volume record. Bioturbation preferentially diminishes the Record of higher-frequency fluctuations (Reference GoreauGoreau 1980, Reference Dalfes, Schneider, Thompson, Berger, Hays, Imbrie and SaltzmanDalfes and others in press), furthermore, we must consider the changing isotopic composition of the ice sheets themselves: the ice sheets were probably isotopically heavier (less negative δ180) at their inception than at their maximum extent (Reference OlaussonOlausson 1981). Thus the apparent record of ice growth inferred from ocean sediment δ180, which implicitly assumes a constant isotopic composition for the ice sheets, will lag the true ice volume record. Estimates based on simple Isotope budgets for the Pleistocene ice sheets indicate that this lag time could be as long as several thousand years; similar effects may create a lag between ice decay and its appearance in the δ180 record (Reference OlaussonOlausson 1981, Reference Mix and RuddimanMix and Ruddiman in press).

More detailed calculations with an ice-sheet/ice-flow model (Reference Covey, Schneider, Berger, Hays, Imbrie and SaltzmanCovey and Schneider in press) imply that the distortions between ice volume and δ180 record may be even greater because in a real ice sheet a large amount of the ice has a very long residence time. Covey and Schneider use a zonally symmetric ice-sheet model with power law creep and instant bedrock adjustment. δ180 of deposition is specified as a function of the height of the ice sheet, and isotopes are advected by the ice flow. Preliminary results for the Antarctic ice sheet are shown in Figure 4. Long after the ice sheet reaches an equilibrium height, a large amount of (relatively) isotopically heavy ice remains trapped below the bedrock level.

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

In summary, it is apparent that the δ180 record from ocean sediment cores primarily reflects the changing ice volume during the Pleistocene. The isotope record is probably good enough to identify the major cycles of glacial/interglacial variations, i.e. the cycle of 106 a and other “Milankovitch peaks”. But caution should be exercised in examining the details, particularly in interpreting phase lags between ice volume and other climatic variables such as temperature, and in “tuning” the results of climate models to correlate with δ180 series.

The National Center for Atmospheric Research is sponsored by the National Science Foundation.

Footnotes

page 44 note * Submitted for publication:

Covey C, Haagenson P L A model of oxygen isotope composition of precipitation: implications for paleoclimate data

References

Berger, W H, Gardner, J V 1975 On the determination of Pleistocene temperatures from planktonic foraminifera. Journal of Fommini feral Research 5: 102113 Google Scholar
Covey, C, Schneider, S H In press Models for reconstructing temperature and ice volume from oxygen isotope data. In Berger, A, Hays, J, Imbrie, J, Saltzman, B (eds) Milankovitch and climate: understanding the response to orbital forcing. Dordrecht, Reldel Publishing Co.Google Scholar
Dalfes, H N, Schneider, S H, Thompson, S L In press Effects of bioturbation on climatic spectra inferred from deep sea cores. In Berger, A, Hays, J, Imbrie, J, Saltzman, B (eds) Milarikovitah and climate: understanding the response to orbital forcing, Dordrecht, Reidel Publishing Co.Google Scholar
Dansgaard, W 1964 Stable isotopes in precipitation. Tellus 16(4): 436468 CrossRefGoogle Scholar
Dansgaard, W, Tauber, H 1969 Glacial oxygen-18 content and Pleistocene ocean temperatures. Science 166(3904): 499502 CrossRefGoogle ScholarPubMed
Dansgaard, W, Johnsen, S J, Clausen, H B, Langway, C C Jr 1971 Climatic record revealed by the Camp Century ice core. In Turekian, K K (ed) The late Cemzois glacial ages. New Haven and London, Yale University Press: 3751 Google Scholar
Emiliani, C 1978 The cause of the ice ages. Earth and Planetary Science Letters 37(3): 349354 Google Scholar
Epstein, S, Buchsbaum, H A, Lowenstam, H A, Urey, H C 1953 Revised carbonate-water isotopic temperature scale. Geological Soeiety of America Bulletin 64: 13151325 Google Scholar
Erez, J, Luz, B 1982 Temperature control of oxygen-isotope fractionation of cultured planktonic foraminifera. Nature 297(5763): 220222 Google Scholar
Goreau, T J 1980 Freguency sensitivity of the deep-sea climatic record, mature 287(5783): 620622 Google Scholar
Hays, J D, Imbrie, J, Shackleton, N J 1976 Variations in the Earth’s orbit: pacemaker of the ice ages. Science 194(4270): 11211132 Google Scholar
Mix, A C, Ruddiman, W F In press Oxygen isotope analyses and Pleistocene ice volumes. Quaternary Research Google Scholar
Olausson, E 1965 Evidence of climatic changes in North Atlantic deep sea cores, with remarks on isotopic paleotemperature analysis. Progress in Oceanography 3: 221252 CrossRefGoogle Scholar
Olausson, E 1981 On the isotopic composition of late Cenozoic sea water. Geogmfiska Annaler 63A(3—4): 311312 Google Scholar
Shackleton, N J 1967 Oxygen isotope analyses and Pleistocene temperatures re-assessed, nature 215(5096): 1517 CrossRefGoogle Scholar
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).