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J. A. Robbins

Publications and source records attributed to J. A. Robbins.

6 recordsLinked to original sources
USGS2016

Stepped-combustion 14C dating of bomb carbon in lake sediment

In this study, we applied a stepped-combustion approach to dating post-bomb lake sediment from north-central Mississippi. Samples were combusted at a low temperature (400 °) and then at 900 °. The CO 2 was collected separately for both combustions and analyzed. The goal of this work was to develop a methodology to improve the accuracy of 14 C dating of sediment by combusting at a lower temperature and reducing the amount of reworked carbon bound to clay minerals in the sample material. The 14 C fraction modern results for the low and high temperature fractions of these sediments were compared with well-defined 137 Cs determinations made on sediment taken from the same cores. Comparison of “bomb curves” for 14 C and 137 Cs indicate that low temperature combustion of sediment improved the accuracy of 14 C dating of the sediment. However, fraction modern results for the low temperature fractions were depressed compared to atmospheric values for the same time frame, possibly the result of carbon mixing and the low sedimentation rate in the lake system.

Radiocarbon↗
USGS2000

Time-averaged fluxes of lead and fallout radionuclides to sediments in Florida Bay

Recent, unmixed sediments from mud banks of central Florida Bay were dated using 210 Pb/ 226 Ra, and chronologies were verified by comparing sediment lead temporal records with Pb/Ca ratios in annual layers of coral ( Montastrea annularis ) located on the ocean side of the Florida Keys. Dates of sediment lead peaks (1978±2) accord with prior observations of a 6 year lag between the occurrence of maximum atmospheric lead in 1972 and peak coral lead in 1978. Smaller lags of 1–2 years occur between the maximum atmospheric radionuclide fallout and peaks in sediment temporal records of 137 Cs and Pu. Such lags are consequences of system time averaging (STA) in which atmospherically delivered particle-associated constituents accumulate and mix in a (sedimentary?) reservoir before transferring to permanent sediments and coral. STA model calculations, using time-dependent atmospheric inputs, produced optimized profiles in excellent accord with measured sediment 137 Cs, Pu, lead, and coral lead distributions. Derived residence times of these particle tracers (16±1, 15.7±0.7, 19±3, and 16±2 years, respectively) are comparable despite differences in sampling locations, in accumulating media, and in element loading histories and geochemical properties. For a 16 year weighted mean residence time, STA generates the observed 6 year lead peak lag. Evidently, significant levels of nondegradable, particle-associated contaminants can persist in Florida Bay for many decades following elimination of external inputs. Present results, in combination with STA model analysis of previously reported radionuclide profiles, suggest that decade-scale time averaging may occur widely in recent coastal marine sedimentary environments.

Florida↗
USGS1996

Uranium-series disequilibrium, sedimentation, diatom frustules, and paleoclimate change in Lake Baikal

The large volume of water, approximately one-fifth of the total surface fresh water on the planet, contained in Lake Baikal in southeastern Siberia is distinguished by having a relatively high concentration of uranium (ca. 2 n M ), and, together with the surface sediments, an unusually high 234 U 238 U alpha activity ratio of 1.95. About 80% of the input of uranium to the lake, with a 234 U 238 U ratio of 2.0, comes from the Selenga River. Profiles of uranium, as well as the extent of isotopic disequilibrium in a 9 m sediment core collected on Academic Ridge, generally show high values during interglacial periods corresponding to high diatom frustule numbers (DiFr) and biogenic silica (BSi) data that have been reported elsewhere. During glacial periods (low DiFr and BSi), uranium progeny ( 234 U and 230 Th) were in secular equilibrium with low concentrations of their parent 238 U. Radionuclide distributions were interpreted in terms of a quantitative model allowing for adsorption of riverine inputs of uranium onto two classes of sedimenting particles with differing 238 U 232 Th ratios and uranium progeny in secular equilibrium. If the 234 U 238 U activity ratio of adsorbed uranium has remained constant, mean sedimentation rates can be independently estimated as 3.6 ± 0.6 and 3.7 ± 0.9 cm · kyr −1 for the decay of 234 U and in-growth of 230 Th, respectively. These rates are consistent with a mean rate of 3.76 cm · kyr −1 , calculated by optimization of the correspondence between adsorbed 238 U and δ 18 O in dated oceanic sediments. The adsorbed uranium apparently tracks variable river flow during interglacials and is drastically reduced during periods of glaciation. Evidently, uranium has not been significantly redistributed within Baikal sediments over at least the past 250 kyr and is a unique, biologically non-essential, tracer for climate-sensitive processes, which provide their own internal geochronometers, potentially useful for ages up to 1 Myr BP.

Earth and Planetary Science Letters↗
USGS1995

A summary of the effects of mining and related activities on the sediment-trace element geochemistry of Lake Coeur d'Alene, Idaho, USA

During 1989 and 1990 a series of 12 gravity cores, and 150 surface grab samples were collected in Lake Coeur d'Alene, Idaho to determine trace element concentrations, partitioning and surface and subsurface distribution patterns in the bed sediments of the lake. In addition, selected subsamples from one core were analyzed for 117 Cs activity to begin to establish a trace element geochemical history for the lake. The intent was to try and relate the trace element concentrations and distributions in the sediment column to past and present mining and mining related activities in the area. Substantial portions of the surface and near-surface sediments in Lake Coeur d'Alene are markedly enriched in Ag, As, Cd, Hg, Pb, Sb and Zn, and somewhat enriched in Cu, Fe and Mn. Surface distribution patterns, as well as variations in the thickness of the trace element-rich subsurface sediments, indicate that the source of much of this enriched material is the Coeur d'Alene River. The similarity between the trace element-rich surface and subsurface sediments with respect to: their location, their bulk chemistry, and their trace element partitioning indicate that the sources and/or concentrating mechanisms causing the trace element enrichment in the lake sediments probably have been the same throughout their depositional history. An estimated 75 million metric tons of trace element-rich sediments have been deposited on or in the lakebed. Based on a Mt. St. Helens' ash layer from the 1980 eruption, ages estimated from 137 Cs activity, and the presence of 80 discernible and presumably annual layers in a core collected near the Coeur d'Alene River delta, indicate that the deposition of trace element-rich sediments began, at least in the Coeur d'Alene River delta, some time between 1895 and 1910, dates consistent with the onset of mining and ore-processing activities that began in the area in the 1880's.

Journal of Geochemical Exploration↗
USGS1993

The Effect of mining and related activities on the sediment-trace element geochemistry of Lake Coeur d'Alene, Idaho, U.S.A.; Part II, Subsurface sediments

During the summer of 1990, 12 gravity cores were collected in Lake Coeur d'Alene, Idaho, at various depths and in a variety of depositional environments. All core subsamples were analyzed to determine bulk chemistry and selected subsamples were analyzed for trace-element partitioning and (137)Cs activity. The purpose of these analyses was to determine the trace-element concentrations and distributions in the sediment column and to try to establish a trace-element geochemical history of the lake in relation to mining and mining-related discharge operations in the area. Substantial portions of the near-surface sediments in Lake Coeur d'Alene are markedly enriched in Ag, As, Cd, Hg, Pb, Sb, and Zn, and somewhat enriched in Cu, Fe, and Mn. Variations in the thickness of the trace element- rich sediments suggest that the source of much of this material is the Coeur d'Alene River. Calculated estimates indicate that there are some 75 million metric tons of trace element-rich sediments currently on/in the lakebed. Estimated trace-element masses in excess of those caused by non-mining-related sources, range from a high of 468,000 metric tons of Pb to a low of 260 metric tons of Hg. The similarity between the trace element-rich surface and subsurface sediments as regards their: (1) location; (2) bulk chemistry; (3) interelement relationships; and (4) trace-element partitioning indicate that the sources and/or concentrating mechanisms causing the trace-element enrichment in the lake probably have been the same throughout their depositional history. Based on Mt. St. Helens' ash layer from the 1980 eruption, ages estimated from (137)Cs activity, and the presence of 80 discernible and presumably annual layers in a core collected near the Coeur d'Alene River delta, it appears that deposition rates for the trace element-rich sediments varied from 2.1 to 1.3 cm/yr. These data also indicate that the deposition of trace element-rich sediments began, at least in the Coeur d'Alene River delta, sometime between 1895 and 1910, dates consistent with the onset of mining and ore-processing activities in the area which began in the 1880's.

Open-File Report↗