scholarly journals Factors controlling shell carbon isotopic composition of land snail <i>Acusta despecta sieboldiana</i> estimated from laboratory culturing experiment

2014 ◽  
Vol 11 (19) ◽  
pp. 5335-5348 ◽  
Author(s):  
N. Zhang ◽  
K. Yamada ◽  
N. Suzuki ◽  
N. Yoshida

Abstract. The carbon isotopic composition (δ13C) of land snail shell carbonate derives from three potential sources: diet, atmospheric CO2, and ingested carbonate (limestone). However, their relative contributions remain unclear. Under various environmental conditions, we cultured one land snail subspecies, Acusta despecta sieboldiana, collected from Yokohama, Japan, and confirmed that all of these sources affect shell carbonate δ13C values. Herein, we consider the influences of metabolic rates and temperature on the carbon isotopic composition of the shell carbonate. Based on results obtained from previous works and this study, a simple but credible framework is presented to illustrate how each source and environmental parameter affects shell carbonate δ13C values. According to this framework and some reasonable assumptions, we estimated the contributions of different carbon sources for each snail individual: for cabbage-fed (C3 plant) groups, the contributions of diet, atmospheric CO2, and ingested limestone vary in the ranges of 66–80, 16–24, and 0–13%, respectively. For corn-fed (C4 plant) groups, because of the possible food stress (less ability to consume C4 plants), the values vary in the ranges of 56–64, 18–20, and 16–26%, respectively. Moreover, according to the literature and our observations, the subspecies we cultured in this study show preferences towards different plant species for food. Therefore, we suggest that the potential food preference should be considered adequately for some species in paleoenvironment studies. Finally, we inferred that only the isotopic exchange of the calcite-HCO3−-aragonite equilibrium during egg laying and hatching of our cultured snails controls carbon isotope fractionation.

2014 ◽  
Vol 11 (5) ◽  
pp. 6555-6590 ◽  
Author(s):  
N. Zhang ◽  
K. Yamada ◽  
N. Suzuki ◽  
N. Yoshida

Abstract. The carbon isotopic composition (δ13C) of land snail shell carbonate derives from three potential sources: diet, atmospheric CO2, and ingested carbonate (limestone). However, their relative contributions remain unclear. Under various environmental conditions, we cultured one land snail species, Acusta despecta sieboldiana collected from Yokohama, Japan, and confirmed that all of these sources affect shell carbonate δ13C values. Herein, we consider the influences of metabolic rates and temperature on the carbon isotopic composition of the shell carbonate. Based on previous works and on results obtained in this study, a simple but credible framework is presented for discussion of how each source and environmental parameter can affect shell carbonate δ13C values. According to this framework and some reasonable assumptions, we have estimated the contributions of different carbon sources for each snail individual: for cabbage (C3 plant) fed groups, the contributions of diet, atmospheric CO2 and ingested limestone respectively vary as 66–80%, 16–24%, and 0–13%. For corn (C4 plant) fed groups, because of the possible food stress (lower consumption ability of C4 plant), the values vary respectively as 56–64%, 18–20%, and 16–26%. Moreover, we present new evidence that snails have discrimination to choose C3 and C4 plants as food. Therefore, we suggest that food preferences must be considered adequately when applying δ13C in paleo-environment studies. Finally, we inferred that, during egg laying and hatching of our cultured snails, carbon isotope fractionation is controlled only by the isotopic exchange of the calcite–HCO3−–aragonite equilibrium.


2007 ◽  
Vol 52 (3) ◽  
pp. 388-394 ◽  
Author(s):  
ZongXiu Liu ◽  
ZhaoYan Gu ◽  
NaiQin Wu ◽  
Bing Xu

Radiocarbon ◽  
2002 ◽  
Vol 44 (3) ◽  
pp. 755-760 ◽  
Author(s):  
Jeffrey S Pigati

Correcting the 14C age of a sample for fractionation is straightforward if the measured carbon was derived entirely from the atmosphere, either directly or through chemical and/or biological reactions that originated with atmospheric carbon. This correction is complicated in the case of gastropods that incorporate carbon from limestone or secondary carbonate (e.g. soil carbonate) during shell formation. The carbon isotopic composition of such gastropod shells is determined by fractionation, as well as mixing of carbon from sources with different isotopic values. Only the component of shell carbonate derived from atmospheric carbon should be corrected for fractionation. In this paper, the author derives a new expression for correcting the measured 14C activity of gastropod shells for fractionation, and describe an iterative approach that allows the corrected 14C activity and the fraction of shell carbonate derived from atmospheric carbon to be determined simultaneously.


Nature ◽  
1992 ◽  
Vol 357 (6378) ◽  
pp. 461-466 ◽  
Author(s):  
Bruno D. Marino ◽  
Michael B. McElroy ◽  
Ross J. Salawitch ◽  
W. Geoffrey Spaulding

2010 ◽  
Vol 7 (9) ◽  
pp. 2959-2973 ◽  
Author(s):  
J. W. H. Weijers ◽  
G. L. B. Wiesenberg ◽  
R. Bol ◽  
E. C. Hopmans ◽  
R. D. Pancost

Abstract. Branched Glycerol Dialkyl Glycerol Tetraethers (GDGTs) are membrane spanning lipids synthesised by as yet unknown bacteria that thrive in soils and peat. In order to obtain more information on their ecological niche, the stable carbon isotopic composition of branched GDGT-derived alkanes, obtained upon ether bond cleavage, has been determined in a peat and various soils, i.e. forest, grassland and cropland, covered by various vegetation types, i.e., C3- vs. C4-plant type. These δ13C values are compared with those of bulk organic matter and higher plant derived n-alkanes from the same soils. With average δ13C values of −28‰, branched GDGTs in C3 soils are only slightly depleted (ca. 1‰) relative to bulk organic carbon and on average 8.5‰ enriched relative to plant wax-derived long-chain n-alkanes ( nC29–nC33). In an Australian soil dominantly covered with C4 type vegetation, the branched GDGTs have a δ13C value of −18‰, clearly higher than observed in soils with C3 type vegetation. As with C3 vegetated soils, branched GDGT δ13C values are slightly depleted (1‰) relative to bulk organic carbon and enriched (ca. 5‰) relative to n-alkanes in this soil. The δ13C values of branched GDGT lipids being similar to bulk organic carbon and their co-variation with those of bulk organic carbon and plant waxes, suggest a heterotrophic life style and assimilation of relatively heavy and likely labile substrates for the as yet unknown soil bacteria that synthesise the branched GDGT lipids. However, a chemoautotrophic lifestyle, i.e. consuming respired CO2, could not be fully excluded based on these data alone. Based on a natural labelling experiment of a C3/C4 crop change introduced on one of the soils 23 years before sampling and based on a free-air CO2 enrichment experiment with labelled CO2 on another soil, a turnover time of ca. 18 years has been estimated for branched GDGTs in these arable soils.


2010 ◽  
Vol 7 (3) ◽  
pp. 3691-3734 ◽  
Author(s):  
J. W. H. Weijers ◽  
G. L. B. Wiesenberg ◽  
R. Bol ◽  
E. C. Hopmans ◽  
R. D. Pancost

Abstract. Branched Glycerol Dialkyl Glycerol Tetraethers (GDGTs) are membrane spanning lipids synthesised by as yet unknown bacteria that thrive in soils and peat. In order to obtain more information on their ecological niche, the stable carbon isotopic composition of branched GDGT-derived alkanes, obtained upon ether bond cleavage, has been determined in various soils, i.e. peat, forest, grassland and cropland, covered by various vegetation types, i.e., C3- vs. C4-plant type. These δ13C values are compared with those of bulk organic matter and higher plant derived n-alkanes from the same soils. With average δ13C values of −28‰, branched GDGTs in C3 soils are only slightly depleted (ca. 1‰) relative to bulk organic carbon and on average 8.5‰ enriched relative to plant wax-derived long-chain n-alkanes (nC29–nC33). In an Australian soil covered with C4 type vegetation, the branched GDGTs have a δ13C value of −18‰, clearly higher than observed in soils with C3 type vegetation. As with C3 vegetated soils, branched GDGT δ13C values are slightly depleted (1‰) relative to bulk organic carbon and enriched (ca. 5‰) relative to n-alkanes in this soil. The δ13C values of branched GDGT lipids being similar to bulk organic carbon and their co-variation with those of bulk organic carbon and plant waxes, suggest a heterotrophic life style and assimilation of relatively heavy and likely labile substrates for the as yet unknown soil bacteria that synthesise the branched GDGT lipids. However, a chemoautotrophic lifestyle, i.e. consuming respired CO2, could not be fully excluded based on these data alone. Based on a natural labelling experiment of a C3/C4 crop change introduced on one of the soils 23 years before sampling and based on a free air CO2 enrichment experiment with labelled CO2 on another soil, a turnover time of ca. 17 years has been estimated for branched GDGTs in these arable soils.


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