Sc. Armstrong et al., STRONTIUM ISOTOPIC EVIDENCE ON THE CHEMICAL EVOLUTION OF PORE WATERS IN THE MILK RIVER AQUIFER, ALBERTA, CANADA, Applied geochemistry, 13(4), 1998, pp. 463-475
Strontium isotope ratios were measured on 13 rock, 18 leachate and 28
pore-water samples from the Milk River aquifer, the confining argillac
eous formations, and the glacial till mantling the recharge area. Stro
ntium isotope ratios (Sr-87/Sr-86) of pore waters from the aquifer, co
nfining units, and the glacial till ranged from 0.7069 to 0.7082. The
87Sr/86Sr ratios in aquifer pore waters decrease with increasing dista
nce from the aquifer recharge area, and this is interpreted to be the
result of mixing and water-rock interaction within the aquifer. The so
lute composition of the recharging groundwater is modified by the loca
l lithology, causing distinct geochemical patterns along different flo
w paths within the aquifer. Whole-rock Sr-87/Sr-86 ratios indicate tha
t the shales and till are generally more radiogenic than the aquifer s
andstone. The authigenic carbonate cements and rock-forming minerals c
omprising the major lithologic units had little apparent influence on
the pore-water Sr chemistry. Carbonate cement leachates from the till
and the aquifer sandstone are more radiogenic than those from the conf
ining shale formations. Feldspar separates from the aquifer sandstone
have relatively radiogenic Sr isotope ratios, whereas bentonites from
the Milk River and Colorado Shale Formations have whole-rock and leach
ate Sr isotope ratios that are relatively unradiogenic. Ratios of most
Milk River aquifer pore waters are lower than those of any leachates
or whole rocks analyzed, except the bentonites. The Sr-87/Sr-86 ratios
of exchangeable Sr in the bentonites are similar to ratios found in t
he more evolved pore waters. Simple rock-water interaction models calc
ulated for the whole-rock, leachate, and exchangeable-ion/pore-water p
airs indicate that ion exchange with bentonite clays within the Milk R
iver and Colorado Shale Formations appears to influence the isotopic e
volution of the pore-water Sr in each of these units. (C) 1998 Elsevie
r Science Ltd. All rights reserved.