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New perspectives on radium behavior within a subterranean estuary

New perspectives on radium behavior within a subterranean estuary
New perspectives on radium behavior within a subterranean estuary
Over the past decade, radium isotopes have been frequently applied as tracers of submarine groundwater discharge (SGD). The unique radium signature of SGD is acquired within the subterranean estuary, a mixing zone between fresh groundwater and seawater in coastal aquifers, yet little is known about what controls Ra cycling in this system. The focus of this study was to examine controls on sediment and groundwater radium activities within permeable aquifer sands (Waquoit Bay, MA, USA) through a combination of field and laboratory studies. In the field, a series of sediment cores and corresponding groundwater profiles were collected for analysis of the four radium isotopes, as well as dissolved and sediment associated manganese, iron, and barium. We found that in addition to greater desorption at increasing salinity, radium was also closely tied to manganese and iron redox cycling within these sediments. A series of laboratory adsorption/desorption experiments helped elucidate the importance of 1) contact time between sediment and water, 2) salinity of water in contact with sediment, 3) redox conditions of water in contact with sediment, and 4) the chemical characteristics of sediment on radium adsorption/desorption. We found that these reactions are rapid (on the order of hours), desorption increases with increasing salinity and decreasing pH, and the presence of Fe and Mn (hydr)oxides on the sediment inhibit the release of radium. These sediments have a large capacity to sorb radium from fresh water. Combined with these experimental results, we present evidence from time series groundwater sampling that within this subterranean estuary there are cyclic periods of Ra accumulation and release controlled by changing salinity and redox conditions.
Radium, Sediments, Desorption, Adsorption, Barium, Submarine groundwater discharge, Subterranean estuary, Redox reactions, Ion exchange, Distribution coefficient
0304-4203
250-267
Gonneea, Meagan Eagle
aed0add0-461a-470d-b7c5-471261966853
Morris, Paul J.
05f4f629-e810-4679-a2c5-73611ce9660f
Dulaiova, Henrieta
436bf4df-0bb6-4bb3-acdd-c9969d52718e
Charette, Matthew A.
afe63d56-266a-4819-9dfb-2669ffb204e7
Gonneea, Meagan Eagle
aed0add0-461a-470d-b7c5-471261966853
Morris, Paul J.
05f4f629-e810-4679-a2c5-73611ce9660f
Dulaiova, Henrieta
436bf4df-0bb6-4bb3-acdd-c9969d52718e
Charette, Matthew A.
afe63d56-266a-4819-9dfb-2669ffb204e7

Gonneea, Meagan Eagle, Morris, Paul J., Dulaiova, Henrieta and Charette, Matthew A. (2008) New perspectives on radium behavior within a subterranean estuary. Marine Chemistry, 109 (3-4), 250-267. (doi:10.1016/j.marchem.2007.12.002).

Record type: Article

Abstract

Over the past decade, radium isotopes have been frequently applied as tracers of submarine groundwater discharge (SGD). The unique radium signature of SGD is acquired within the subterranean estuary, a mixing zone between fresh groundwater and seawater in coastal aquifers, yet little is known about what controls Ra cycling in this system. The focus of this study was to examine controls on sediment and groundwater radium activities within permeable aquifer sands (Waquoit Bay, MA, USA) through a combination of field and laboratory studies. In the field, a series of sediment cores and corresponding groundwater profiles were collected for analysis of the four radium isotopes, as well as dissolved and sediment associated manganese, iron, and barium. We found that in addition to greater desorption at increasing salinity, radium was also closely tied to manganese and iron redox cycling within these sediments. A series of laboratory adsorption/desorption experiments helped elucidate the importance of 1) contact time between sediment and water, 2) salinity of water in contact with sediment, 3) redox conditions of water in contact with sediment, and 4) the chemical characteristics of sediment on radium adsorption/desorption. We found that these reactions are rapid (on the order of hours), desorption increases with increasing salinity and decreasing pH, and the presence of Fe and Mn (hydr)oxides on the sediment inhibit the release of radium. These sediments have a large capacity to sorb radium from fresh water. Combined with these experimental results, we present evidence from time series groundwater sampling that within this subterranean estuary there are cyclic periods of Ra accumulation and release controlled by changing salinity and redox conditions.

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More information

Published date: 16 April 2008
Keywords: Radium, Sediments, Desorption, Adsorption, Barium, Submarine groundwater discharge, Subterranean estuary, Redox reactions, Ion exchange, Distribution coefficient

Identifiers

Local EPrints ID: 54667
URI: http://eprints.soton.ac.uk/id/eprint/54667
ISSN: 0304-4203
PURE UUID: 29657d67-d536-4093-9559-6e641a1c6912

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Date deposited: 17 Jul 2008
Last modified: 15 Mar 2024 10:49

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Contributors

Author: Meagan Eagle Gonneea
Author: Paul J. Morris
Author: Henrieta Dulaiova
Author: Matthew A. Charette

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