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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 2014 Nov 3;111(45):E4809. doi: 10.1073/pnas.1418161111

Reply to Maxwell et al.: Stable isotopes and their potential for interpreting archaeobotanical remains

Simone Riehl a,b,1, Konstantin E Pustovoytov a,c
PMCID: PMC4234542  PMID: 25368142

We thank Maxwell et al. (1) for their interest in our study and agree that multielement isotopic analysis helps interpret ancient agricultural systems. Measurements of δ15N on archaeobotanical crop seeds have corroborated hypotheses of Near Eastern cultivation under gradually less-fertile soil conditions (2) and that early farmers used livestock manure to enhance crop yields (3). It is also understood that soil fertility along with salinity, evapotranspiration, and crop density causes variation in δ13C.

However, by stating that δ13C data from archaeological cereal grains is unsuited to “distinguish between variation in nitrogen and water availability,” Maxwell et al. introduce some misapprehension that we believe must be removed.

Maxwell et al. refer to δ13C variation of 2.6‰ in barley caused by different sources of nitrogen in soil (1). These data have been obtained from greenhouse plants. In contrast, field experiments in the Near East demonstrated that the carbon isotope ratios in cereal grain and pulse seeds are largely unaffected by manuring (4). This was even stated in the work that Maxwell et al. use to support their argument (3). In figure 1B of Maxwell et al., δ15N and δ13C data on barley from a Neolithic site in Greece (red squares) are plotted on the δ15N ranges of experimentally manured cereals (for original data, see ref. 3). The Δ13C data on barley from the Neolithic site range between 18‰ and 19.2‰. The variation of 1.2‰ corroborates our model of smaller δ13C ranges at coastal locations or in areas of higher precipitation (5).

In addition, we interpreted our δ13C data from ancient barley clearly for their mean and their minima values, using intrasite variation of up to 6‰ (figure 5 in ref. 5), and not 1‰ as claimed by Maxwell et al. (1). The range between 16‰ and 17‰ is considered as a transitional area from signals of well-watered individuals (>17‰) to reduced water availability (<16‰), as described in our methods section.

Furthermore, the similarity of the carbon isotope signal in coevally charred barley grains and wood charcoals from archaeological sites strongly suggests a predominance of climate forcing in δ13C responses of barley (2).

We therefore agree that δ15N measurements on archaeobotanical crop seeds are useful to address local specifics of ancient agricultural practice, but they are of minor importance for our supraregional approach to patterns of past water availability.

Maxwell et al. further suggest the use of δ18O to obtain information on the water status in relation with possible irrigation (1). Although oxygen is a useful physiological proxy in modern plants, it suffers from strong fractionation during charring of the plant remains. This is decisive for the applicability of the method, as more than 90% of the plant remains in archaeological sites are preserved through charring. Only in rare cases is biogenic carbonate present in some seed coats (Celtis spp. and Lithospermum spp.), and only in this case can δ18O of the carbonate fraction be used for paleoenvironmental reconstruction (6).

Footnotes

The authors declare no conflict of interest.

References

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