A quantitative model for describing the within‐population variation in planktonic foraminifer shell chemistry that results from secondary calcification and selective dissolution is presented. The objective is to construct a basis for inferring the chemistries of different shell components and estimating the extent of shell dissolution. Variation is modeled as mixtures of two kinds of shell calcite, a primary calcite that forms the chambers and a secondary calcite that forms crust. Bulk shell chemistries are intermediate between the chemistries of these calcites and lie on mixing lines between them. For two component systems, mass balance relationships can be reformulated as a linear regression and solved for the chemistries of the primary and secondary calcites and for the uncertainties associated with these estimates. To apply this model, one needs measurements of bulk shell chemistries and estimates of the relative proportions of secondary and primary calcites. For most planktonic foraminifer species the proportion of secondary calcite can be estimated from differences in the relationship between shell size and mass before and after crusting. Preliminary results are consistent with previous work showing that secondary calcites are added at depth. However, even deep‐dwelling species appear to grow most of their primary shell in surface waters and some surface‐dwelling species add secondary calcite in the deep ocean. In contrast to the model's simple description of secondary calcification, the variation in chemistry from selective dissolution is more complicated because undissolved shells are themselves mixtures of primary and secondary calcites and therefore present a wide range of initial shell compositions. Nevertheless, the model allows both the compositions of different components to be inferred and the amount of dissolution to be estimated. Preliminary results indicate that dissolution of planktonic foraminifera is apparent nearly 2 km above the foraminifer lysocline and even apparently well‐preserved shells may be over 50% dissolved.

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Abstract. Using bathymetric transects of surface sediments underlying similar sea surface temperatures but exposed to increasing dissolution, we examined the processes which affect the relationship between foraminiferal Mg/Ca and 5180. We found that Globigerinoides saccculifer calcifies over a relatively large range of water depth and that this is apparent in their Mg content. On the seafloor, foraminiferal Mg/Ca is substantially altered by dissolution with the degree of alteration increasing with water depth. Selective dissolution of the chamber calcite, formed in surface waters, shifts the shell's bulk Mg/Ca and 5180 toward the chemistries of the secondary crust acquired in colder thermocline waters. The magnitude of this shift depends on both the range of temperatures over which the shell calcified and the degree to which it is subsequently dissolved. In spite of this shift the initial relationship between Mg/Ca and 5180, determined by their temperature dependence, is maintained. We conclude that paired measurements of 5180 and Mg/Ca can be used for reconstructing 518Owater, though care must be taken to determine where in the water column the reconstruction applies.

[1] Paired d 18O and Mg/Ca measurements on the same foraminiferal shells offer the ability to independently estimate sea surface temperature (SST) changes and assess their temporal relationship to the growth and decay of continental ice sheets. The accuracy of this method is confounded, however, by the absence of a quantitative method to correct Mg/Ca records for alteration by dissolution. Here we describe dissolution-corrected calibrations for Mg/Ca-paleothermometry in which the preexponent constant is a function of size-normalized shell weight: (1) . The new calibrations improve the accuracy of SST estimates and are globally applicable. With this correction, eastern equatorial Atlantic SST during the Last Glacial Maximum is estimated to be 2.9°± 0.4°C colder than today.

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