TY - JOUR
T1 - Environmental Controls on Groundwater Chemistry in an Offshore Island Aquifer
T2 - Fiesta Key, Florida
AU - Machusak, Donald D.
AU - Kump, Lee R.
N1 - Funding Information:
Financial support for this research was provided by the U. S. Geological Survey (E.A. Shinn, Principal Investigator), the American Association of Petroleum Geologists (awarded to DDM), and the Department of Geosciences at The Pennsylvania State University (PSU). Logistical assistance from J. Swanson, W. Gibbs, R. Craft, and R. Durner of the Keys Marine Laboratory, Long Key, Florida, was also greatly appreciated. Core extraction was made possible by H. Hudson (NOAA), R. Parizek (PSU), and E. Shinn, with operational assistance in the field provided by H. Hudson and S. Ellis (PSU). J. Bodkin and H. Gong in the Materials Characterization Laboratory at PSU provided laboratory space and analytical equipment. XRD analysis was performed by Tanya Baker, at the PSU Materials Research Laboratory. Data collection was under the assistance of the Field Methods class of 1983: M. Al-Mugheiry, S. Altman, J. Bologa, K. Burkett, D. Cox, P. Fawcett, D. Follweiler, K. Gibbs, W. Kapsner, D. Leppold, M. Martinez, T. Maher, T. Miller, M. Pagani, R. Pancost, S. Petsch, R. Robinson, J. Simmons, K. Yuhas, and especially C. Machusak. Collectively their field assistance made it possible to present the quantity of data included in this study. M. Arthur, R. Parizek, W. White and an anonymous reviewer provided helpful reviews.
PY - 1997
Y1 - 1997
N2 - A field study was undertaken on the Florida Bay side of Fiesta Key, Florida, to identify the chemical characteristics of a previously unexplored offshore groundwater system and to define the critical parameters affecting groundwater movement and interaction with sediment pore fluids and bedrock. Emphasis was placed on the upper 2 meters of bedrock, where groundwater recharge and discharge potentials are maximized, along a 100 meter transect extending from the island margin. Bedrock cores were used to describe Pleistocene depositional textures, and were sampled at discrete depths to determine the extent of water-rock interaction. Piezometers installed into each core hole were used to monitor surface and ground water tide levels, and for the systematic collection of water samples for a large suite of chemical determinations. Aqueous chemical data indicate that these groundwaters are marine in origin, anoxic, and moderately hypersaline (S = 36-40). Exchange of bedrock pore fluids with overlying Bay waters is restricted by a layer of Holocene sediment and a discontinuous soilstone crust formed at the modern bedrock surface. Groundwater chemistry near the sediment/bedrock interface is marked by elevated concentrations of total alkalinity and Ca2+, and by significant Mg2+ depletion. These waters likely acquired their unusual chemistry by mixing between deeper groundwaters and overlying, early diagenetically altered, sediment porewaters. High alkalinity and calcium concentrations presumably result from the combination of the effects of aerobic metabolism, carbonate dissolution, and sulfate reduction. Mg-depletion most likely resulted from the precipitation of Mg-calcite. These unusual chemistries disappear by 2 m depth in the groundwater system, where Ca2+ and Mg2+ concentrations are similar to those expected for seawater under slightly hypersaline conditions. The Pleistocene bedrock contains low Mg, Sr, F, and P concentrations relative to the overlying unconsolidated Holocene carbonate sediments. This is consistent with the diagenetic recrystallization processes that the bedrock has undergone. Hydraulic conditions favor the net recharge of Florida Bay seawater to the groundwater system, but there are insufficient tide data to identify cyclical water exchange rates or groundwater flow patterns.
AB - A field study was undertaken on the Florida Bay side of Fiesta Key, Florida, to identify the chemical characteristics of a previously unexplored offshore groundwater system and to define the critical parameters affecting groundwater movement and interaction with sediment pore fluids and bedrock. Emphasis was placed on the upper 2 meters of bedrock, where groundwater recharge and discharge potentials are maximized, along a 100 meter transect extending from the island margin. Bedrock cores were used to describe Pleistocene depositional textures, and were sampled at discrete depths to determine the extent of water-rock interaction. Piezometers installed into each core hole were used to monitor surface and ground water tide levels, and for the systematic collection of water samples for a large suite of chemical determinations. Aqueous chemical data indicate that these groundwaters are marine in origin, anoxic, and moderately hypersaline (S = 36-40). Exchange of bedrock pore fluids with overlying Bay waters is restricted by a layer of Holocene sediment and a discontinuous soilstone crust formed at the modern bedrock surface. Groundwater chemistry near the sediment/bedrock interface is marked by elevated concentrations of total alkalinity and Ca2+, and by significant Mg2+ depletion. These waters likely acquired their unusual chemistry by mixing between deeper groundwaters and overlying, early diagenetically altered, sediment porewaters. High alkalinity and calcium concentrations presumably result from the combination of the effects of aerobic metabolism, carbonate dissolution, and sulfate reduction. Mg-depletion most likely resulted from the precipitation of Mg-calcite. These unusual chemistries disappear by 2 m depth in the groundwater system, where Ca2+ and Mg2+ concentrations are similar to those expected for seawater under slightly hypersaline conditions. The Pleistocene bedrock contains low Mg, Sr, F, and P concentrations relative to the overlying unconsolidated Holocene carbonate sediments. This is consistent with the diagenetic recrystallization processes that the bedrock has undergone. Hydraulic conditions favor the net recharge of Florida Bay seawater to the groundwater system, but there are insufficient tide data to identify cyclical water exchange rates or groundwater flow patterns.
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U2 - 10.1023/A:1009648200301
DO - 10.1023/A:1009648200301
M3 - Article
AN - SCOPUS:0343329373
SN - 1380-6165
VL - 3
SP - 129
EP - 167
JO - Aquatic Geochemistry
JF - Aquatic Geochemistry
IS - 2
ER -