External 4He sources have been invoked to explain 4He concentrations in groundwater greater than those expected from in situ U and Th production. In a fractured aquifer of Ordovician age located in the St. Lawrence Lowlands (Quebec, Canada), 4He concentrations of up to 4.48 × 10−5 cm3 STP
gnormalH2O−1 were measured. Such concentrations are ∼1000 times higher than would be expected from in situ production. A concomitant increase in 4He concentration and 234U/238U activity ratio is shown, suggesting a common release process in groundwater for 234U and 4He. This process has tentatively been identified as glaciation‐induced rock fracturing following the Laurentide Ice Sheet retreat. The resulting increase in exposed grain surface facilitates 234U release by α‐recoil and that of radiogenic 4He by diffusion. Using a model of helium diffusion from a spherical grain, it is shown that rock fracturing facilitated the release of accumulated 4He at rates ranging from 4.2 × 10−10 to 1.06 × 10−8 cm3 STP
gnormalH2O−1 yr−1. These release rates are between 1000 and 30,000 times higher than the local U and Th steady state production rate, of 3.5 ± 1.4 × 10−13 cm3 STP
grock−1 yr−1. Integration of 4He release rates over time yields a radiogenic 4He concentration of between 3.85 × 10−6 and 7.12 × 10−5 cm3 STP
gnormalH2O−1, in the range of concentrations measured in the St. Lawrence Lowlands fractured aquifers. Results support the occurrence of a local radiogenic helium source to explain the excesses measured in groundwater without requiring a significant external He crustal flux.