Stable carbon isotope composition (δ13C) of land snail materials is widely used as a proxy for reconstructing past vegetation and environmental changes. Interpretation δ13C data is challenging due to the complexities of snail physiology. This study cultured Lissachatina fulica (Bowdich, 1822) snails to investigate δ13C of their soft tissues and excrement under various plant types and dietary carbonate content. Our results show that snails primarily assimilate organic matter (OM), with limited use of dietary carbonates. δ13C of organic matter in excrement correlates positively with that in the diet, but exhibits deviations due to variable carbon isotopic fractionation during assimilation. Tissue δ13C (δ13Ctissue) is positively related to the δ13C of OM (δ13COM) in the diet, varying by turnover rates, with faster turnover rate, such as the digestive gland, exhibiting more negative δ13Ctissue values. Moreover, carbon isotopic fractionation between tissues and diet (Δ13Ctissue-OM) differs based on plant type. Snails fed with C3 plants show positive Δ13Ctissue-OM values, whereas those fed with C4 plants exhibit negative values. These Δ13Ctissue-OM values are far from equilibrium (Δ13Ctissue-OM = 0) with conditions of rapid snail growth. Our findings indicate that the snails fed with C3 and C4 plants result in distinct carbon isotopic fractionation, leading to the deviation in δ13C between plants and land snail materials (e.g., excrement, tissues, shells and shell-bound organic matter). A comprehensive model of carbon metabolism and isotopic fractionation in snails is proposed including the assimilation process from diet to soft tissues and excretion. This study highlights the importance of physiological factors such as growth rates and turnover rates when interpreting δ13C of land snail materials for paleoenvironmental reconstructions.
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