Geology topics

R.G. Deike

Publications and source records attributed to R.G. Deike.

3 recordsLinked to original sources

USGS1997

Formation of ferric iron crusts in Quaternary sediments of Lake Baikal, Russia, and implications for paleoclimate

Phosphate-bearing, ferric iron and siliceous crusts ranging in age from Recent to approximately 65,000 yr B.P. are observed in sediments of Lake Baikal. In younger sediments the crusts are at the base of a spectrum of secondary iron and manganese oxides that accumulate near the sediment/water interface in the zone of positive oxidation potential beneath an oxygenated water column. In areas where the average Quaternary sedimentation rates have been slow (e.g. 0.026 mm/yr), the crusts are more common, and span a wider range of ages. No crusts have been found where the Quaternary sedimentation mode has been deltaic and rapid (0.15 mm/yr). Independent core correlation based on magnetic properties of the sediment suggests that crusts can be correlated over most of Academician Ridge, an area that is particularly sensitive to climatic events affecting the concentration of suspended sediment. These crusts may be indicative of periods of low suspended sediment concentration, which occur during sustained transitions from glacial periods of high detrital input, to interglacial periods of high diatom sedimentation. The crusts are dominated by iron-rich and siliceous amorphous mineral phases, with an FeO:SiO2 by weight of 3:1. Regardless of age or location in the lake the Fe phase always includes Ca, P and Mn. Extensive microprobe data for these four elements recast as normalized elemental weight percent reveal linear trends of Ca:P and Fe:P. With increasing P, Ca also increases such that the two elements maintain a linear relationship passing very close to the origin and with a mean molar Ca:P=0.3 (too low for well-characterized apatite). Conversely, with increasing P, Fe decreases (mean molar Fe:P=3.4). There is no correlation between Mn and P. Molar Fe:P ratios for vivianite (an Fe(II) phosphate mineral observed in sediments closely below some crusts) are clustered around a stoichiometric composition. The covariant increase in Ca:P and the corresponding decrease in Fe:P may be explained by: (1) coupled adsorption of aqueous Ca and P by a colloidal ferric hydrous oxide; (2) loss of Fe from a Ca-P-Fe phase; or (3) oxidation of vivianite to a metastable mineral phase that gradually loses Ca and gains Fe. The first explanation is favored, because there is no petrographic evidence for either the existence of an originating Ca-P-Fe phase, or, for the oxidation of vivianite. Further, it is suggested that by continually equalizing surface charge, Ca allows more phosphate to be adsorbed leading to thicker crusts and longer preservation after burial.

Marine Geology↗

USGS1990

Dolomite dissolution rates and possible Holocene dedolomitization of water-bearing units in the Edwards aquifer, south-central Texas

Rates of dolomite dissolution can be used to test the concept, based on geomorphologic evidence, that a major part of the Edwards aquifer could have formed within the Holocene, a timeframe of approximately 10,000 years. During formation of the aquifer in the Edwards limestone (Cretaceous, Albian) of the Balcones fault zone, dolomite dissolution and porosity development were synchronous and the result of mixing-zone dedolomitization. Initiation of the mixing zone in the early Holocene (∼11,000 years before present) is suggested by the maximum age of formation of major discharge sites that allowed the influx of meteoric water into brine-filled, dolomitic preaquifer units. Dedolomitization, the dissolution of dolomite and net precipitation of calcite, has left aquifer units that are calcitic, and 40 vol.% interconnected pore space. The mass of dolomite missing is obtained by comparison of stratigraphically equivalent altered and unaltered units. One dissolution rate (1.76 × 10 −4 mmol dolomite kg H2O −1 yr −1 ) is determined from this mass, 10 4 yr reaction time, and a log-linear function describing the increase in mass discharge (three orders of magnitude) during aquifer formation. The second estimated dissolution rate is obtained from the mass transfer of dolomite to solution calculated from the increase in magnesium in pore fluids selected from the modern aquifer to represent a typical flowpath during aquifer formation. A reaction time of 10 4 yr for this mass transfer yields a rate of 0.56 × 10 −4 mmol dolomite kg H2O −1 yr −1 Both of these rates are comparable to modern rates of dolomite dissolution (0.3 to 4.5 × 10 −4 mmol dolomite kg H2O −1 yr −1 ) calculated from measured reaction times in the Tertiary Floridan aquifer system in Florida and the Madison aquifer in the Mississippian Madison Limestone of the Northern Great Plains. Similarity of these rates to the estimated paleo-rates of dolomite dissolution supports a 10 4 yr reaction timeframe. Both of these rates are comparable to modern rates of dolomite dissolution (0.3 to 4.5 × 10 −4 mmol dolomite kg H2O −1 yr −1 ) calculated from measured reaction times in the Tertiary Floridan aquifer system in Florida and the Madison aquifer in the Mississippian Madison Limestone of the Northern Great Plains. Similarity of these rates to the estimated paleo-rates of dolomite dissolution supports a 10 4 yr reaction timeframe. The Holocene reaction time also can be compared to a series of reaction times calculated by assuming that the mass of dolomite missing from the Edwards was removed at rates observed in the Floridan and Madison aquifers. These reaction times (for complete removal of dolomite) range from 2700 to 58,500 yr and span the Pleistocene-Holocene boundary. Finally, an estimated dolomite reaction rate during dedolomitization of the Edwards aquifer based on surface area of exposed dolomite [mmol cm −2 s −1 (millimoles per square centimeter per second)] may be approximated from reaction times. This rate is directly a function of the mass of dolomite removed and the surface area exposed per pore volume passing through the rock. The surface area is available from the observed dolomite rhomb size in unaltered rock. The rate of pore fluid movement is obtained from the averaged annual discharge. Rates during formation of the Edwards aquifer calculated from all reaction times range from 10 −13 to 10 −14 mmol dolomite cm −2 s −1 . These rates are faster than rates (10 −18 mmol cm −2 s −1 ), measured in the pure laboratory system, CaMg(CO 3 ) 2 CO 2 H 2 O, but slower than rates determined in an alpine stream study (10 −10 to 10 −11 mmol cm −2 s −1 ) where cold glacial melt water flows over dolostone. Dolomite dissolution rates from both the Edwards and other aquifers support the concept that a major part of the Edwards aquifer could have formed within the Holocene.

Texas↗

USGS1971

A geochemical hypothesis for dolomitization by ground water

Most modern disordered dolomite has been found in dynamic environments. However, solutions associated with modern dolomite formation do not have a common Mg/Ca ratio; the ratio ranges from about 3 to 100. Ground-water circulation may have a significant role in formation of regional dolomites; one of the primary requirements for regional dolomite formation is a large supply of magnesium ions. An X-ray study of well cuttings from the Tertiary limestone aquifer of central Florida indicates that it is composed primarily of calcite and dolomite with minor amounts of quartz and apatite. The magnesium content of the calcite is slightly lower (0-2 percent MgC03) in the recharge areas than in the deeper confined parts of the aquifer system (2-4 percent MgC03). Our data support other recent work and indicate an equilibrium constant for dolomite of 2 X 10-17. Inasmuch as this value is exactly the square of the calcite equilibrium constant (10~8-35), the Mg/Ca ratio must be unity for the three-phase equilibrium, calcite-dolomite-water. The Mg/Ca ratio in water from the aquifer is as low as 0.05 in the recharge area where the water is also undersaturated with respect to both calcite and dolomite. With time and length of travel path in the system, the water increases systematically in Mg/Ca ratio, which approaches unity; saturation with respect to the two carbonates also increases downgradient until the solution apparently becomes over-saturated with respect to both carbonates. In Tertiary limestones of the Yucatan Peninsula, the Mg/Ca range in water is similar to that for Florida. The small amount of magnesium available from the solution of magnesium calcites and dolomite in the potable zone of active circulation is insufficient to provide the amount required for extensive dolomitization unless enormous quantities of rock are available for dissolution. However, dolomite may be forming in the zones of brackish water that underlie the Florida and Yucatan Peninsulas. The required magnesium may be derived from the readily available ocean water or reflux brines as the hydrologic regimen is changed because of relative fluctuations of sea level.

Florida↗