Geology topics

Liang-Feng Han

Publications and source records attributed to Liang-Feng Han.

3 recordsLinked to original sources

USGS2014

The curved 14 C vs. δ 13 C relationship in dissolved inorganic carbon: A useful tool for groundwater age- and geochemical interpretations

Determination of the 14 C content of dissolved inorganic carbon (DIC) is useful for dating of groundwater. However, in addition to radioactive decay, the 14 C content in DIC ( 14 C DIC ) can be affected by many geochemical and physical processes and numerous models have been proposed to refine radiocarbon ages of DIC in groundwater systems. Changes in the δ 13 C content of DIC (δ 13 C DIC ) often can be used to deduce the processes that affect the carbon isotopic composition of DIC and the 14 C value during the chemical evolution of groundwater. This paper shows that a curved relationship of 14 C DIC vs. δ 13 C DIC will be observed for groundwater systems if (1) the change in δ 13 C value in DIC is caused by a first-order or pseudo-first-order process, e.g. isotopic exchange between DIC and solid carbonate, (2) the reaction/process progresses with the ageing of the groundwater, i.e. with decay of 14 C in DIC, and (3) the magnitude of the rate of change in δ 13 C of DIC is comparable with that of 14 C decay. In this paper, we use a lumped parameter method to derive a model based on the curved relationship between 14 C DIC and δ 13 C DIC . The derived model, if used for isotopic exchange between DIC and solid carbonate, is identical to that derived by Gonfiantini and Zuppi (2003). The curved relationship of 14 C DIC vs. δ 13 C DIC can be applied to interpret the age of the DIC in groundwater. Results of age calculations using the method discussed in this paper are compared with those obtained by using other methods that calculate the age of DIC based on adjusted initial radiocarbon values for individual samples. This paper shows that in addition to groundwater age interpretation, the lumped parameter method presented here also provides a useful tool for geochemical interpretations, e.g. estimation of apparent rates of geochemical reactions and revealing the complexity of the geochemical environment.

Chemical Geology↗

USGS2013

Revision of Fontes & Garnier's model for the initial 14 C content of dissolved inorganic carbon used in groundwater dating

The widely applied model for groundwater dating using 14 C proposed by Fontes and Garnier (F&G) (Fontes and Garnier, 1979) estimates the initial 14 C content in waters from carbonate-rock aquifers affected by isotopic exchange. Usually, the model of F&G is applied in one of two ways: (1) using a single 13 C fractionation factor of gaseous CO 2 with respect to a solid carbonate mineral, εg/s, regardless of whether the carbon isotopic exchange is controlled by soil CO 2 in the unsaturated zone, or by solid carbonate mineral in the saturated zone; or (2) using different fractionation factors if the exchange process is dominated by soil CO 2 gas as opposed to solid carbonate mineral (typically calcite). An analysis of the F&G model shows an inadequate conceptualization, resulting in underestimation of the initial 14 C values ( 14 C 0 ) for groundwater systems that have undergone isotopic exchange. The degree to which the 14 C 0 is underestimated increases with the extent of isotopic exchange. Examples show that in extreme cases, the error in calculated adjusted initial 14 C values can be more than 20% modern carbon (pmc). A model is derived that revises the mass balance method of F&G by using a modified model conceptualization. The derivation yields a “global” model both for carbon isotopic exchange dominated by gaseous CO 2 in the unsaturated zone, and for carbon isotopic exchange dominated by solid carbonate mineral in the saturated zone. However, the revised model requires different parameters for exchange dominated by gaseous CO 2 as opposed to exchange dominated by solid carbonate minerals. The revised model for exchange dominated by gaseous CO 2 is shown to be identical to the model of Mook (Mook, 1976). For groundwater systems where exchange occurs both in the unsaturated zone and saturated zone, the revised model can still be used; however, 14 C 0 will be slightly underestimated. Finally, in carbonate systems undergoing complex geochemical reactions, such as oxidation of organic carbon, radiocarbon ages are best estimated by inverse geochemical modeling techniques.

Chemical Geology↗

USGS2012

A graphical method to evaluate predominant geochemical processes occurring in groundwater systems for radiocarbon dating

A graphical method is described for identifying geochemical reactions needed in the interpretation of radiocarbon age in groundwater systems. Graphs are constructed by plotting the measured 14 C, δ 13 C, and concentration of dissolved inorganic carbon and are interpreted according to specific criteria to recognize water samples that are consistent with a wide range of processes, including geochemical reactions, carbon isotopic exchange, 14 C decay, and mixing of waters. The graphs are used to provide a qualitative estimate of radiocarbon age, to deduce the hydrochemical complexity of a groundwater system, and to compare samples from different groundwater systems. Graphs of chemical and isotopic data from a series of previously-published groundwater studies are used to demonstrate the utility of the approach. Ultimately, the information derived from the graphs is used to improve geochemical models for adjustment of radiocarbon ages in groundwater systems.

Chemical Geology↗