Radium geochemistry of ground waters in Paleozoic carbonate aquifers, midcontinent, USA

Citation
Nc. Sturchio et al., Radium geochemistry of ground waters in Paleozoic carbonate aquifers, midcontinent, USA, APPL GEOCH, 16(1), 2001, pp. 109-122
Citations number
64
Categorie Soggetti
Earth Sciences
Journal title
APPLIED GEOCHEMISTRY
ISSN journal
08832927 → ACNP
Volume
16
Issue
1
Year of publication
2001
Pages
109 - 122
Database
ISI
SICI code
0883-2927(200101)16:1<109:RGOGWI>2.0.ZU;2-V
Abstract
The purpose of this study was to elucidate the processes controlling the di stribution and behavior of the longer-lived Ra isotopes in continuous Paleo zoic carbonate aquifers of parts of Missouri, Kansas, and Oklahoma. Activit ies of (Ra-228) and (Ra-226) were analyzed in fresh and saline ground water s, brines, and rocks. The fluids have a wide salinity range (200-250,000 mg l(-1) total dissolved solids). The (Ra-226) activity ranges from 0.66-7660 dpm kg(-1) and correlates with salinity and other alkaline earth element ( Ca, Sr, and Ba) concentrations. The range of (Ra-228:Ra-226) ratios in the fluids (0.06-1.48) is similar to that in the aquifer rocks (0.21-1.53). The relatively low mean fluid (Ra-228:Ra-226) ratio (0.30) reflects the low Th :U ratio of the predominant carbonate aquifer rock. Radium occurs mostly (g reater than or equal to 77%) as Ra2+ species in the fluids. Salinity-depend ent sorption-desorption processes (with log K values from 10(0)-10(4) and n egatively correlated with salinity), involving Th-enriched surface coatings on aquifer flow channels, can explain the rapid solid-fluid transfer of Ra isotopes in the system and the correlation of Ra with salinity. (C) 2000 E lsevier Science Ltd. All rights reserved.