Geology topics

E. Callender

Publications and source records attributed to E. Callender.

At least 19 recordsLinked to original sources

USGS2007

The chemical response of particle-associated contaminants in aquatic sediments to urbanization in New England, U.S.A.

Relations between urbanization and particle-associated contaminants in New England were evaluated using a combination of samples from sediment cores, streambed sediments, and suspended stream sediments. Concentrations of PAHs, PCBs, DDT, and seven trace metals (Cd, Cr, Cu, Hg, Ni, Pb, Zn) were correlated strongly with urbanization, with the strongest relations to percentage commercial, industrial, and transportation (CIT) land use. Average PAH and metal concentrations in the most urbanized watersheds were approximately 30 and 6 times the reference concentrations, respectively, in remote, undeveloped watersheds. One-quarter to one-half of sampling sites had concentrations of PAHs, Cu, Pb, or Zn above the probable effects concentration, a set of sediment quality guidelines for adverse effects to aquatic biota, and sediments were predicted to be toxic, on average, when CIT land use exceeded about 10%. Trends in metals in cores from urban watersheds were dominantly downward, whereas trends in PAHs in a suburban watershed were upward. A regional atmospheric-fallout gradient was indicated by as much as order-of-magnitude-greater concentrations and accumulation rates of contaminants in cores from an undeveloped reference lake in Boston compared to those from remote reference watersheds. Contaminant accumulation rates in the lakes with urbanization in their watersheds, however, were 1-3 orders of magnitude greater than those of reference lakes, which indicate the dominance of local sources and fluvial transport of contaminants to urban lakes. These analyses demonstrate the magnitude of urban contamination of aquatic systems and air sheds, and suggest that, despite reductions in contaminant emissions in urban settings, streams and lakes will decline in quality as urbanization of their watersheds takes place. ?? 2006 Elsevier B.V. All rights reserved.

Journal of Contaminant Hydrology↗

USGS2007

Bottom sediments and pore waters near a hydrothermal vent in Lake Baikal (Frolikha Bay)

We discuss the redox environments and the compositions of bottom sediments and sedimentary pore waters in the region of a hydrothermal vent in Frolikha Bay, Lake Baikal. According to our results, the submarine vent and its companion nearby spring on land originate from a common source. The most convincing evidence for their relation comes from the proximity of stable oxygen and hydrogen isotope compositions in pore waters and in the spring water. The isotope composition indicates a meteoric origin of pore waters, but their major- and minor-element chemistry bears imprint of deep water which may seep through permeable faulted crust. Although pore waters near the submarine vent have a specific enrichment in major and minor constituents, hydrothermal discharge at the Baikal bottom causes a minor impact on the lake water chemistry, unlike the case of freshwater geothermal lakes in the East-African Rift and North America. ?? 2007.

Russian Geology and Geophysics↗

USGS2007

Elements of the iron and manganese cycles in Lake Baikal

Using data obtained in recent years, we considered the external mass balance and characteristics of internal iron and manganese cycles in Lake Baikal (biological uptake, remineralization, sedimentary and diffusive fluxes, accumulation in sediments, time of renewal, etc.). Some previous results and common concepts were critically reevaluated. ?? Pleiades Publishing, Ltd. 2007.

Geochemistry International↗

USGS2006

Trends in metals in urban and reference lake sediments across the United States, 1970 to 2001

Trends in metals concentrations in sediment cores from 35 reservoirs and lakes in urban and reference settings were analyzed to determine the effects of three decades of legislation, regulation, and changing demographics and industrial practices in the United States on concentrations of metals in the environment. Decreasing trends outnumber increasing trends for all seven metals analyzed (Cd, Cr, Cu, Pb, Hg, Ni, and Zn). The most consistent trends are for Pb and Cr: For Pb, 83% of the lakes have decreasing trends and 6% have increasing trends; for Cr, 54% of the lakes have decreasing trends and none have increasing trends. Mass accumulation rates of metals in cores, adjusted for background concentrations, decrease from the 1970s to the 1990s, with median changes ranging from -46% (Pb) to -3% (Hg and Zn). The largest decreases are from lakes in dense urban watersheds where the overall metals contamination in recently deposited sediments has decreased to one-half its 1970s median value. However, anthropogenic mass accumulation rates in dense urban lakes remain elevated over those in lakes in undeveloped watersheds, in some cases by as much as two orders of magnitude (Cr, Cu, and Zn), indicating that urban fluvial source signals can overwhelm those from regional atmospheric sources. ?? 2006 SETAC.

Environmental Toxicology and Chemistry↗

USGS2006

The role of biological uptake in iron and manganese cycling in Lake Baikal

The role of biological uptake in the internal cycling of Fe and Mn in Lake Baikal was quantified. Biological uptake, sedimentation consisting of the biogenic and lithogenic fluxes, and remineralization have been evaluated. The results of calculations show that about 5-10% of Fe and Mn accumulated in the lake are annually taken up by biota. More than 80% of this amount is again recycled after remineralization of biological material. At this, the biogenic fluxes of Fe and Mn are 2-4 times less compared to lithogenic ones. Thus not only is oxidation of Fe and Mn within the water column highly enriched in the oxygen that results in settling of Fe and Mn oxides, but also intensive biological uptake of these elements contributes to their fast removal from internal cycling. However, essential remineralization makes this process of minor importance to Fe and Mn cycling in Lake Baikal. ?? Springer 2006.

Conference Paper↗

USGS2005

Historical backcasting of metal concentrations in the Chattahoochee River, Georgia: Population growth and environmental policy

The impact of increasing urbanization on the quality of a river system has been investigated by examining the current concentration of trace metals in the Chattahoochee River south of Atlanta, GA, and comparing these to previously published historical sediment data from reservoirs along the river. The lack of historical data for dissolved metal concentrations prior to ???1980 requires an approach using these historic metal data from sediment cores. Core data are combined with current suspended load and dissolved metal data to "backcast" dissolved metal concentrations in the metro-Atlanta portion of the Chattahoochee River. The data suggest that the per capita input of dissolved trace metals have actually decreased since the 1920s, but anthropogenic inputs of metal are still a substantial water quality issue. ?? 2005 Elsevier Ltd. All rights reserved.

Applied Geochemistry↗

USGS2004

Tire-wear particles as a source of zinc to the environment

Tire-tread material has a zinc (Zn) content of about 1 wt %. The quantity of tread material lost to road surfaces by abrasion has not been well characterized. Two approaches were used to assess the magnitude of this nonpoint source of Zn in the U.S. for the period 1936−1999. In the first approach, tread-wear rates from the automotive engineering literature were used in conjunction with vehicle distance-driven data from the U.S. Department of Transportation to determine Zn releases. A second approach calculated this source term from the volume of tread lost during lifetime tire wear. These analyses showed that the quantity of Zn released by tire wear in the mid-1990s was of the same magnitude as that released from waste incineration. For 1999, the quantity of Zn released by tire wear in the U.S. is estimated to be 10 000−11 000 metric tons. A specific case study focused on Zn sources and sinks in an urban−suburban watershed (Lake Anne) in the Washington, DC, metropolitan area for a time period of the late 1990s. The atmospheric flux of total Zn (wet deposition) to the watershed was 2 μg/cm 2 /yr. The flux of Zn to the watershed estimated from tire wear was 42 μg/cm 2 /yr. The measured accumulation rate of total Zn in age-dated sediment cores from Lake Anne was 27 μg/cm 2 /yr. These data suggest that tire-wear Zn inputs to urban−suburban watersheds can be significantly greater than atmospheric inputs, although the watershed appears to retain appreciable quantities of vehicular Zn inputs.

Environmental Science & Technology↗

USGS2000

Geochemical effects of rapid sedimentation in aquatic systems: Minimal diagenesis and the preservation of historical metal signatures

Rapid sedimentation exerts a pronounced influence on early sedimentary diagenesis in that there is insufficient time for a sediment particle to equilibrate in any one sediment layer before that layer may be displaced vertically by another layer. These sedimentation patterns are common in surface-water reservoirs whose sedimentation rates (1-10 cm yr-1) are several orders of magnitude greater than those for natural lakes (0.01-0.5 cm yr-1). Two examples of the effects of rapid sedimentation on geochemical metal signatures are presented here. Interstitial-water data (Fe) from two sites in the Cheyenne River Embayment of Lake Oahe on the Missouri River illustrate the effects of changing sedimentation rates on dissolved species. Rapid burial during high-flow yrs appears to limit early sedimentary diagenesis to aerobic respiration. Solid-phase metal data (Pb) from a site in Pueblo Reservoir on the upper Arkansas River in Colorado appear to record historical releases by flooding of abandoned mine sites upstream in Leadville, Colorado. Interstitial-water ammonia and ferrous Fe data indicate that at least one interval at depth in the sediment where solid metal concentrations peak is a zone of minimal diagenesis. The principal diagenetic reactions that occur in these sediments are aerobic respiration and the reduction of Mn and Fe oxides. Under slower sedimentation conditions, there is sufficient time for particulate organic matter to decompose and create a diagenetic environment where metal oxides may not be stable. The quasi-steady-state interstitial Fe profiles from Tidal Potomac River sediments are an example of such a situation. This occurs primarily because the residence time of particles in the surficial sediment column is long enough to allow benthic organisms and bacteria to perform their metabolic functions. When faster sedimentation prevails, there is less time for these metabolic reactions to occur since the organisms do not occupy a sediment layer for any length of time. Also, the quantity and quality of the organic matter input to the sediment layer is important in that reservoirs often receive more terrestrial organic matter than natural lakes and this terrestrial organic matter is generally more refractory than autochthonous aquatic organic matter.

Journal of Paleolimnology↗

USGS1999

Greigite (Fe3S4) as an indicator of drought - The 1912-1994 sediment magnetic record from White Rock Lake, Dallas, Texas, USA

Combined magnetic and geochemical studies were conducted on sediments from White Rock Lake, a reservoir in suburban Dallas (USA), to investigate how land use has affected sediment and water quality since the reservoir was filled in 1912. The chronology of a 167-cm-long core is constrained by the recognition of the pre-reservoir surface and by 137Cs results. In the reservoir sediments, magnetic susceptibility (MS) and isothermal remanent magnetization (IRM) are largely carried by detrital titanomagnetite that originally formed in igneous rocks. Titanomagnetite and associated hematite are the dominant iron oxides in a sample from the surficial deposit in the watershed but are absent in the underlying Austin Chalk. Therefore, these minerals were transported by wind into the watershed. After about 1960, systematic decreases in Ti, Fe, and Al suggest diminished input of detrital Fe-Ti oxides from the surficial deposits. MS and IRM remain constant over this interval, however, implying compensation by an increase in strongly magnetic material derived from human activity. Anthropogenic magnetite in rust and ferrite spherules (from fly ash?) are more common in sediment deposited after about 1970 than before and may account for the constant magnetization despite the implied decrease in detrital Fe-Ti oxides. An unexpected finding is the presence of authigenic greigite (Fe3S4), the abundance of which is at least partly controlled by climate. Greigite is common in sediments that predate about 1975, with zones of concentration indicated by relatively high IRM/MS. High greigite contents in sediment deposited during the early to mid-1950s and during the mid-1930s correspond to several-year periods of below-average precipitation and drought from historical records. Relatively long water-residence times in the reservoir during these periods may have led to elevated levels of sulfate available for bacterial sulfate reduction. The sulfate was probably derived via the oxidation of pyrite that is common in the underlying Austin Chalk. These results provide a basis for the paleoenvironmental interpretation of greigite occurrence in older lake sediments. The results also indicate that greigite formed rapidly and imply that it can be preserved in the amounts produced over a short time span (in this lake, only a few years). This finding thus suggests that, in some lacustrine settings, greigite is capable of recording paleomagnetic secular variation.

Journal of Paleolimnology↗

USGS1997

Historical trends in organochlorine compounds in river basins identified using sediment cores from reservoirs

This study used chemical analyses of dated sediment cores from reservoirs to define historical trends in water quality in the influent river basins. This work applies techniques from paleolimnology to reservoirs, and in the process, highlights differences between sediment-core interpretations for reservoirs and natural lakes. Sediment cores were collected from six reservoirs in the central and southeastern United States, sectioned, and analyzed for 137Cs and organochlorine compounds. 137Cs analyses were used to demonstrate limited post-depositional mixing, to indicate sediment deposition dates, and to estimate sediment focusing factors. Relative lack of mixing, high sedimentation rates, and high focusing factors distinguish reservoir sediment cores from cores collected in natural lakes. Temporal trends in concentrations of PCBs, total DDT (DDT + DDD + DDE), and chlordane reflect historical use and regulation of these compounds and differences in land use between reservoir drainages. PCB and total DDT core burdens, normalized for sediment focusing, greatly exceed reported cumulative regional atmospheric fallout of PCBs and total DDT estimated using cores from peat hogs and natural lakes, indicating the dominance of fluvial inputs of both groups of compounds to the reservoirs.This study used chemical analyses of dated sediment cores from reservoirs to define historical trends in water quality in the influent river basins. This work applies techniques from paleolimnology to reservoirs, and in the process, highlights differences between sediment-core interpretations for reservoirs and natural lakes. Sediment cores were collected from six reservoirs in the central and southeastern United States, sectioned, and analyzed for 137Cs and organochlorine compounds. 137Cs analyses were used to demonstrate limited post-depositional mixing, to indicate sediment deposition dates, and to estimate sediment focusing factors. Relative lack of mixing, high sedimentation rates, and high focusing factors distinguish reservoir sediment cores from cores collected in natural lakes. Temporal trends in concentrations of PCBs, total DOT (DDT+DDD+DDE), and chlordane reflect historical use and regulation of these compounds and differences in land use between reservoir drainages. PCB and total DDT core burdens, normalized for sediment focusing, greatly exceed reported cumulative regional atmospheric fallout of PCBs and total DDT estimated using cores from peat bogs and natural lakes, indicating the dominance of fluvial inputs of both groups of compounds to the reservoirs.

Environmental Science & Technology↗

USGS1997

Biogeochemical phosphorus mass balance for Lake Baikal, southeastern Siberia, Russia

Extensive data for Lake Baikal have been synthesized into a geochemical mass balance for phosphorus (P). Some of the P budget and internal cycling terms for Baikal have been compared to similar terms for oligotrophic Lake Superior, mesotrophic Lake Michigan and the Baltic Sea, and the Ocean. Lake Baikal has a large external source of fluvial P compared to the Laurentian upper Great Lakes and the Ocean. The major tributary to Lake Baikal has experienced substantial increases in organic P loading during the past 25 years. This, coupled with potential P inputs from possible phosphorite mining, may threaten Baikal's oligotrophic status in the future. Water-column remineralization of particulate organic P is substantially greater in Lake Baikal than in the Laurentian Great Lakes. This is probably due to the great water depths of Lake Baikal. There is a gradient in P burial efficiency, with very high values (80%) for Lake Baikal and Lake Superior, lower values (50%) for Lake Michigan and the Baltic Sea, and a low value (13%) for the Ocean. The accumulation rate of P in Lake Baikal sediments is somewhat greater than that in the Laurentian upper Great Lakes and the Baltic Sea, and much greater than in the Ocean. Benthic regeneration rates are surprisingly similar for large lacustrine and marine environments and supply less than 10% of the P utilized for primary production in these aquatic environments.

Marine Geology↗

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↗

USGS1997

Water-quality trends in White Rock Creek Basin from 1912-1994 identified using sediment cores from White Rock Lake Reservoir, Dallas, Texas

Historical trends in selected water-quality variables from 1912 to 1994 in White Rock Creek Basin were identified by dated sediment cores from White Rock Lake. White Rock Lake is a 4.4-km2 reservoir filled in 1912 and located on the north side of Dallas, Texas, with a drainage area of 259 km2. Agriculture dominated land use in White Rock Creek Basin before about 1950. By 1990, 72% of the basin was urban. Sediment cores were dated using cesium-137 and core lithology. Major element concentrations changed, and sedimentation rates and percentage of clay-sized particles in sediments decreased beginning in about 1952 in response to the change in land use. Lead concentrations, normalized with respect to aluminum, were six times larger in sediment deposited in about 1978 than in pre-1952 sediment. Following the introduction of unleaded gasoline in the 1970s, normalized lead concentrations in sediment declined and stabilized at about two and one-half times the pre-1952 level. Normalized zinc and arsenic concentrations increased 66 and 76%, respectively, from before 1952 to 1994. No organochlorine compounds were detected in sediments deposited prior to about 1940. Concentrations of polychlorinated biphenyls (PCB) and DDE (a metabolite of DDT) increased rapidly beginning in the 1940s and peaked in the 1960s at 21 and 20 ??g kg-1, respectively, which is coincident with their peak use in the United States. Concentrations of both declined about an order of magnitude from the 1960s to the 1990s to 3.0 and 2.0 ??g kg-1, respectively. Chlordane and dieldrin concentrations increased during the 1970s and 1980s. The largest chlordane concentration was 8.0 ??g kg-1 and occurred in a sediment sample deposited in about 1990. The largest dieldrin concentration was 0.7 ??g kg-1 and occurred in the most recent sample deposited in the early 1990s. Agricultural use of chlordane and dieldrin was restricted in the 1970s; however, both were used as termiticides, and urban use of chlordane continued at least until 1990. Recent use of dieldrin and aldrin, which degrades to dieldrin, has not been reported; however, increasing trends in dieldrin since the 1970s suggest recent urban use could have occurred.

Journal of Paleolimnology↗

USGS1997

Geochemical mass balances of major elements in Lake Baikal

Major element mass balances for Lake Baikal are calculated with mostly previously published data for soluble fluxes and new, unpublished data for riverine suspended particulate matter chemistry. Physical transport seems to be the most important riverine process. The elements Ca, Mg, and Na seem to be very mobile in the weathering mantle and K and Si seem to be relatively mobile. A comparison of elemental input-output budgets and mass accumulation rates (MAR) in bottom sediments shows that most major elements, except Ca, Si, and Mn, have comparable riverine particulate matter fluxes and MARs. The addition of wet atmospheric deposition fluxes results in an excess of Ca, Mg, and Na entering the lake. The additive effect of these excess inputs during a 40-year period amounts to undetectable concentration increases in the water column. If erosion of weathered bedrock is the source of most dissolved and all particulate matter transported to the lake, theoretical elemental fluxes can be calculated with Al as the conservative element. Flux ratios (observed/theoretical) range from 0.7 to 2.2, but most fall within the acceptable range of 0.7-1.5. Major rock-forming elements are carried by rivers as weathering products and there are minimal biogeochemical processes that modify these inputs as suspended particulate matter accumulates in the bottom sediments of the lake.

Limnology and Oceanography↗

USGS1996

Identifying water-quality trends in the Trinity River, Texas, USA, 1969-1992, using sediment cores from Lake Livingston

Chemical analyses were done on cores of bottom sediment from three locations in Lake Livingston, a reservoir on the Trinity River in east Texas to identify trends in water quality in the Trinity River using the chemical record preserved in bottom sediments trapped by the reservoir. Sediment cores spanned the period from 1969, when the reservoir was impounded, to 1992, when the cores were collected. Chemical concentrations in reservoir sediment samples were compared to concentrations for 14 streambed sediment samples from the Trinity River Basin and to reported concentrations for soils in the eastern United States and shale. These comparisons indicate that sediments deposited in Lake Livingston are representative of the environmental setting of Lake Livingston within the Trinity River Basin. Vertical changes in concentrations within sediment cores indicate temporal trends of decreasing concentrations of lead, sodium, barium, and total DDT (DDT plus its metabolites DDD and DDE) in the Trinity River. Possible increasing temporal trends are indicated for chlordane and dieldrin. Each sediment-derived trend is related to trends in water quality in the Trinity River or known changes in environmental factors in its drainage basin or both.

Texas↗

USGS1992

Thermal springs in Lake Baikal

Pore waters extracted from sediment cores were analyzed for their oxygen and hydrogen isotopic compositions and major ion chemistry to determine the source of water from a vent area for diffuse lake-bottom thermal springs or seeps in Frolikha Bay, northeastern Lake Baikal. The δ 18 O values of pore waters range from -15.2‰ to -16.7‰, and δD values range from -119‰ to -126‰ (both isotopes determined relative to standard mean ocean water [SMOW]). Bottom water in Lake Baikal has a δ 18 O value of -5.6‰ and a δD value of -120‰ Pore waters in the vent area are significantly enriched in Mg, B, Ca, and especially Na and have the lowest δD and δ 18 O values; these pore waters are isotopically and chemically distinct from pore waters in other, more typical parts of the lake. The pore-water isotopic data fall on a local meteoric water line, and covariations in water isotopes and chemistry are not consistent with evaporation or hydrothermal water-rock interaction. The thermal springs represent discharging meteoric waters that have been gently heated during subsurface circulation and are largely unaltered isotopically. Chemical variations are most likely due to dissolution of subsurface evaporites.

Geology↗

USGS1988

The effect of mining on the sediment - trace element geochemistry of cores from the Cheyenne River arm of Lake Oahe, South Dakota, U.S.A.

Six cores, ranging in length from 1 to 2 m, were collected in the Cheyenne River arm of Lake Oahe, South Dakota, to investigate potential impacts from gold-mining operations around Lead, South Dakota. Sedimentation rates in the river arm appear to be event-dominated and rapid, on the order of 6-7 cm yr.-1. All the chemical concentrations in the core samples fall within the wide ranges previously reported for the Pierre Shale of Cretaceous age and with the exception of As, generally are similar to bed sediment levels in the Cheyenne River, Lake Oahe and Foster Bay. Based on the downcore distribution of Mn, it appears that reducing conditions exist in the sediment column of the river arm below 2-3 cm. The reducing conditions do not appear to be severe enough to produce differentiation of Fe and Mn throughout the sediment column in the river arm. Cross-correlations for high-level metal-bearing strata within the sediment column can be made for several strata and for several cores; however, cross-correlations for all the high-level metal-bearing strata are not feasible. As is the only element which appears enriched in the core samples compared to surface sediment levels. Well-crystallized arsenopyrite was found in high-As bearing strata from two cores and probably was transported in that form from reducing sediment-storage sites in the banks or floodplains of Whitewood Creek and the Belle Fourche River. It has not oxidized due to the reducing conditions in the sediment column of the Cheyenne River arm. Some As may also be transported in association with Fe- and Mn-oxides and -hydroxides, remobilized under the reducing conditions in the river arm, and then reprecipitated in authigenic sulfide phases. In either case, the As appears to be relatively immobile in the sediment column. ?? 1988.

Chemical Geology↗

USGS1983

Authigenic vivianite in Potomac River sediments: control by ferric oxy-hydroxides

Sand-size particles of vivianite (Fe 3 (PO 4 ) 2 .8H 2 O) have been identified in surficial sediments of the tidal Potomac River near a major sewage treatment plant. Vivianite is concentrated in a surface layer of coarse-sand dredge spoil, which overlies much finer sediment. Although saturation indices indicate that the pore waters of virtually all the sediments in the study area are supersaturated with respect to vivianite, it is found only in association with dredge spoil. Pore-water profiles of Fe, P, and Eh, and the size and morphology of individual grains, indicate that the vivianite is authigenic. The major control on the occurrence of the mineral is the presence or absence of amorphous ferric oxy-hydroxides, which react with pore-water phosphorus to form stable ferric hydroxy-phosphates preferentially to the formation of vivianite.--Modified journal abstract.

Journal of Sedimentary Petrology↗