The chemical composition, in particular the stable oxygen isotope and Mg/Ca ratio, of its shell is often used to reconstruct subsurface ocean conditions (Groeneveld & Chiessi, 2011;Moffa-Sánchez et al., 2014;Santos et al., 2020). The morphospecies G. inflata contains two different genotypes, with type I associated with subtropical waters in both hemispheres and type II restricted to the subpolar waters of the southern hemisphere (Morard et al., 2011). Subtle differences in shell morphology in G. inflata are thought to reflect this genotypic variation (Morard et al., 2016). However, the two morphotypes are not distinguished in paleoceanographic studies despite different ecological preferences, which may affect their seasonal or vertical habitat and hence chemical composition (Morard et al., 2013). It is also possible (or suspected) that biological differences between the types of G. inflata may induce differences in biomineralization and hence cause their geochemical proxy signals to differ, irrespective of their ecology. In other words, it is unknown if grown under the same conditions, genotype I and II would have the same or different chemical composition. There are indications from other species that genotypes may have different seasonal or vertical habitat preferences (Marshall et al., 2015) as well as for genotypical controls on shell composition (Sadekov et al., 2016). However, despite the obvious implications for paleoceanographic reconstructions, no studies exist that investigate the influence of cryptic diversity on the geochemistry of G. inflata.Next to the unresolved issue of a possible effect of cryptic diversity on its geochemistry, G. inflata is a species that forms a crust that often covers most of the lamellar calcite. In many species of foraminifera such crusts may account for a significant proportion of the shell mass and since crusts may have a markedly