Groundwater Dating with 3H - 3He
 

The earlier discussion leaves us with the impression that our ability to produce quantitative tritium ages for groundwaters is fading as fast as the thermonuclear bomb peak. However, by measuring 3H together with its daughter 3He, true ages can be determined through calculations that do not rely on the complicated tritium input function. The drawback to this approach is that 3He is not a routinely sampled nor measured isotope (Clarke et al., 1976). The method was first introduced to the field of hydrogeology in 1979 (Torgersen et al., 1979). Schlosser et al. (1988) provide an excellent review and application and Ekwurzel et al. (1994) compare this technique with dating based on chlorofluorocarbons (CFCs) and 85Kr .
 

Helium-tritium systematics

The decay of tritium from an initial concentration 3Ho after some time t is predicted by:

3Ht = 3Ho elt However, determining t requires that we know 3Ho. The decay of tritium leads to an ingrowth of 3He, which would then be: 3Het = 3Ho(1– elt) By combining both equations, we can cancel the dependency on the input concentration of tritium 3Ho: 3Het = 3Ht(elt –1)  The helium concentration at time t, 3Het, is expressed in TU (1 3He per 1018 H). The measured 3He must be corrected for atmospheric 3He that is dissolved at the time of recharge. Note that atmospheric He is dominantly 4He. This input is assumed to be at equilibrium with the atmosphere, and considers the following points:
  Fig. 7-11 Solubility of noble gases in water (Andrews, 1992).

 
The measured value of 3He, corrected for atmospheric 3He, represents 3He ingrown from 3H decay, and is then used in the dating equation:

t = 12.43/ln2 · ln(1 + [3Het]/[3Ht]) where [3Het]/[3Ht] is the concentration ratio of these two isotopes expressed in tritium units.