Main

Squyres et al. claim1 that their model is misrepresented in our Fig. 1 (ref. 2). However, the apices of the shaded triangle represent not the present composition of the mineral components, but the bulk composition of the potential primary chemical inputs in the sedimentary/evaporite model: a siliciclastic component, sulphate salts precipitated from evaporating groundwater, and iron that may have been mobilized to form haematite. In our Fig. 1 (ref. 2), the composition of the siliciclastic component was represented as basalt, consistent with their descriptions3,4,5,10. Although weathering of silicate minerals is discussed4,5,10, the current mineralogical composition of silicates in the bedrock places no definitive constraints on the chemical composition of the original siliciclastic component; this is because it is inherently unclear whether the current minerals represent primary inputs or secondary alteration products. Consequently, the inferred presence of phyllosilicates and silica4,5,10 cannot be used reliably to constrain the bulk chemical composition of the original siliciclastic input.

Squyres et al.1 suggest that we should have placed one apex of the shaded triangle at the Si + Al end-member (their Fig. 1b), but this is valid only if one of the primary chemical inputs had a bulk composition consisting of just Si + Al. However, the Si:Al ratio is constant throughout Meridiani bedrock3, and both the abundance of SiO2 (48–53% by weight on a sulphur-free basis) and the Si:Al ratio (4.7–5.3) of the bedrocks are nearly identical to martian basalts11 (48–51% by weight SiO2; Si:Al, 3.5–7.2). There is thus no evidence for significant mobilization of Si or Al into the rocks, and Fig. 1b of Squyres et al.1 does not accurately portray primary chemical inputs.

We agree that the current chemical composition of Meridiani bedrock can be accounted for by combining evaporitic and siliciclastic components12. However, this siliciclastic component would have to have been substantially depleted in divalent cations and enriched in Si+Al relative to basalt before it ever interacted with evaporating fluids, not just before it was incorporated into the current outcrop (Fig. 1b). This critical requirement is not discussed in descriptions of the sedimentary/evaporite scenario3,4,5,10, nor has a plausible source for such a large amount of material with this composition been proposed. Furthermore, it would be necessary for evaporating groundwater to add divalent cations to the cation-depleted siliciclastic material in the right proportions to result in their basalt-like chemical compositions12, which seems improbable. The sedimentary/evaporite scenario has significant shortcomings and alternative models2,7 need to be considered.