Ferromanganese oxide deposits from the Central Pacific Ocean,II. Nodules and associated sediments

Bulk chemical, mineralogical and selective leach analyses have been made on a suite of abyssal ferromanganese nodules and associated sediments from the S.W. equatorial Pacific Ocean. Compositional relations between nodules, sediment oxyhydroxides and nearby ferromanganese encrustations are drawn assuming that the crusts represent purely hydrogenetic ferromanganese material. Crusts, δMnO₂-rich nodules and sediment oxyhydroxides are compositionally similar and distinct from diagenetic todorokitebearing nodules. Compared to Fe-Mn crusts, sediment oxyhydroxides are however slightly enriched, relative to Mn and Ni, in Fe, Cu, Zn, Ti and Al, and depleted in Co and Pb, reflecting processes of non-hydrogenous element supply and diagenesis. δMnO₂ nodules exhibit compositions intermediate between Fe-Mn crusts and sediment oxyhydroxides and thus are considered to accrete oxides from both the water column and associated sediments.Deep ocean vertical element fluxes associated with large organic aggregates, biogenic calcite, silica and soft parts have been calculated for the study area. Fluxes associated with organic aggregates are one to three orders of magnitude greater than those associated with the other phases considered, are in good agreement with element accumulation rates in sediments, and are up to four orders of magnitude greater than element accumulation rates in nodules. Metal release from labile biogenic material in surface sediments can qualitatively explain the differences between the composition of Fe-Mn crusts and sediment oxyhydroxides.Todorokite-rich diagenetic nodules are confined to an eastwards widening equatorial wedge. It is proposed that todorokite precipitates directly from interstitial waters. Since the transition metal chemistry of interstitial waters is controlled dominantly by reactions involving the breakdown of organic carbon, the supply and degradation rate of organic material is a critical factor in the formation of diagenetic nodules. The wide range of (trace metal/Mn) ratios observed in marine todorokite reflects a balance between the release of trace metals from labile biogenic phases and the reductive remobilisation of Mn oxide, both of which are related to the breakdown of organic carbon.     

Estimating growth rates of ferromanganese nodules from chemical compositions: implications for nodule formation processes

Using available information on the accretion rates and the bulk chemical compositions of oceanic ferromanganese nodules, it can be shown that the accumulation rate of manganese is proportional to the square of the accumulation rate of iron. This relationship has been used to derive an equation that predicts nodule growth rates from their chemical compositions. The equation accurately predicts growth rates up to about 50 mm/10⁶ yr, but yields incorrect rates for faster-growing concretions. From this relationship nodules underneath water of high primary productivity grow most rapidly and accumulate transition metals most rapidly; however, nodules from regions of highest primary productivity do not have the highest concentrations of nickel and copper. Reduction of manganese within the sediment column and remobilization of a fraction to the surface sediments adds manganese to nodules without substantially augmenting the supply of other transition elements. The addition of remobilized manganese to the nodule dilutes the concentrations of nickel, copper and iron, even though their rates of accumulation are also high.     

Diagenetic mobilization of manganese in Peru Basin sediments

The Mn contents and sedimentation rates of two cores from different areas of the Peru Basin have been determined. The southern core is associated with Mn nodules of conventional slow accretion rates (~ mm/10⁶ yr) while the northern one accompanies nodules with very high growth rates (~10² mm/10⁶ yr). The depletion of Mn observed within the top 40 cm of the cores is interpreted as resulting from a diagenetic remobilization of Mn⁺² due to the oxidative characteristics of the sedimentary column. In both cores, the calculated flux of Mn provided by the sediment is higher than the total Mn recovered in the overlying nodules. This indicates that the Mn content of the Peru Basin nodules can be supplied by diagenetic processes from the sediment, not only for the slowly growing nodules but also for the extremely fast growing concretions found in the north of the basin.     

Thorium and radium isotopic relationships in manganese nodules and sediments at MANOP Site S

Relationships among Th and Ra isotopes in nodule, sediment and water phases at MANOP Site S establish the most likely source for Th in the nodules, the frequency of nodule turning, and the similarity of micro and macro nodules. Manganese nodules and bottom waters have ${}^{230}\text{Th}{}^{232}\text{Th}$ activity ratios considerably higher than other phases at this site suggesting that sea water is the likely source of Th for the nodules. Similar ${}^{230}\text{Th}{}^{232}\text{Th}$ activity ratios in nodule tops and bottoms and in certain cases departure from expected ${}^{226}\text{Ra}{}^{230}\text{Th}$ activity ratios in nodule tops and bottoms indicate that the nodules rotate every one to ten thousand years. The micro nodules have diffusion coefficients of Ra similar to macro nodule bottoms. I suggest that they may act as a carrier phase for transporting metals through oxic sediments to nodules.     

Rare earth element geochemistry of oceanic ferromanganese nodules and associated sediments

Analyses have been made of REE contents of a well-characterized suite of deep-sea (> 4000 m.) principally todorokite-bearing ferromanganese nodules and associated sediments from the Pacific Ocean. REE in nodules and their sediments are closely related: nodules with the largest positive Ce anomalies are found on sediments with the smallest negative Ce anomalies; in contrast, nodules with the highest contents of other rare earths (3 + REE) are found on sediments with the lowest 3 + REE contents and vice versa. ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratios in the nodules (～0.51244) point to an original seawater source but an identical ratio for sediments in combination with the REE patterns suggests that diagenetic reactions may transfer elements into the nodules. Analysis of biogenic phases shows that the direct contribution of plankton and carbonate and siliceous skeletal materials to REE contents of nodules and sediments is negligible. Inter-element relationships and leaching tests suggest that REE contents are controlled by a P-rich phase with a REE pattern similar to that for biogenous apatite and an Fe-rich phase with a pattern the mirror image of that for sea water. It is proposed that 3 + REE concentrations are controlled by the surface chemistry of these phases during diagenetic reactions which vary with sediment accumulation rate. Processes which favour the enrichment of transition metals in equatorial Pacific nodules favour the depletion of 3 + REE in nodules and enrichment of 3 + REE in associated sediments. In contrast, Ce appears to be added both to nodules and sediments directly from seawater and is not involved in diagenetic reactions.     

Do manganese nodules grow or dissolve after burial? Results from the Central Indian Ocean Basin

Fifty buried manganese nodules at different depth intervals were recovered in 12 sediment cores from the Central Indian Ocean Basin (CIOB). A maximum of 15 buried nodules were encountered in one sediment core (AAS-22/GC-07) and the deepest nodule was recovered at 5.50 m below seafloor in core AAS-04/GC-5A. Approximately 80% of the buried nodules are small in size (2 cm diameter) in contrast to the Atlantic Ocean and Peru Basin (Pacific Ocean) where the majority of the buried nodules are large, 8 cm and >6 cm, respectively. Buried nodule size decreases with core depth and this distribution appears to be similar to the phenomenon of “Brazil Nut Effect”. Buried nodules exhibit both smooth and rough surface textures and are ellipsoidal, elongated, rounded, sub rounded, irregular and polynucleated. Buried nodules from siliceous ooze are enriched in Mn, Cu, Ni, Zn, Mo, Ga, V and Rb whereas those from red clay are enriched in Fe, Co, Ti, U, Th, Y, Cr, Nb and Rare Earth Elements (REE). Buried nodules from siliceous ooze suggest their formation under hydrogenetic, early digenetic and diagenetic processes whereas those from red clay are of hydrogenetic origin.REE are enriched more than 1.5 times in buried nodules from red clay compared to siliceous ooze. However, the mode of incorporation of REE into buried nodules from both sedimentary environments is by a single authigenic phase consisting of Fe–Ti–P. Shale-normalized REE patterns and Ce anomalies suggest that nodules from siliceous ooze formed under more oxidizing conditions than those from red clay. Nodules buried at depths between 1.5 and 2.5 m are diagenetic (Mn/Fe ratio 10–15), formed in highly oxic environments (large positive Ce anomalies) and record aeolian dust (high Eu anomalies). Chemical composition, surface texture and morphology of buried nodules are similar to those of surface nodules from the same basin. Furthermore, buried nodule compositions do not exhibit any distinct patterns within the core depth, suggesting that buried nodules neither grow nor dissolve after their burial in the sediment column.     

Geochemistry of ferromanganese nodules from DOMES site a,Northern Equatorial Pacific: Multiple diagenetic metal sources in the deep sea

The major and minor element composition of ferromanganese nodules from DOMES Site A has been determined by X-ray fluorescence methods. Three phases appear to control the bulk compositions: Mn and Fe oxyhydroxides and aluminosilicates. Relatively wide compositional variations are evident throughout the area. Nodules with high Mn/Fe ratios, high Cu, Mg, Mo, Ni and Zn concentrations and high todorokite/δ-MnO₂ ratios have granular surface textures and are confined to an east-west trending depression with thin Quaternary sediment cover. Nodules with low Mn/Fe ratios, high concentrations of As, Ca, Ce, Co, La, P, Sr, Ti, V, Y and Zr and low todorokite/δ-MnO₂ ratios have smooth surfaces and are confined to shallower areas with relatively thick Quaternary sediment to the north and south of the depression.All nodules in the area have compositions which are influenced by diagenesis, but those with the most marked diagenetic signature (high Mn/Fe and Cu/Ni ratios, low Ce/La ratios and more todorokite) are found in areas of very slow or non-existent sedimentation; many of these nodules are actually in contact with outcropping Tertiary sediment. This paradox may be resolved by postulating, by analogy with some shallow-water occurrences, that the nodules accrete from bottom waters which have enhanced particulate and dissolved metal contents derived from diagenetic reaction in areas remote from the site of nodule formation. The metals are supplied in a bottom flow (probably Antarctic Bottom Water) which also erodes, or prevents modern sedimentation in, the depression. Nodules on the flanks of the depression are not evidently affected by this flow and derive at least pan of their constituent metals from diagenetic reaction in the underlying Quaternary sediment.Apparently, abyssal diagenetic nodules can have an immediate and a remote diagenetic metal source. Metal fluxes derived from pore water dissolved metal gradients may not be relevant to particular accreting nodules if a significant fraction of their metals is derived from outside the area in which they form.     

Comparative geochemistry of cadmium, rhenium, uranium, and molybdenum in continental margin sediments

The concentrations of authigenic phases of Cd, Re, U, and Mo increase with depth in four 45-cm-long sediment box cores collected along the axis of the Laurentian Trough, Gulf of St. Lawrence. Average authigenic accumulation rates, estimated from element inventories, are similar to rates in other continental margin environments. Strong regional variations in sediment accumulation rate and sulfide concentration have little influence on the accumulation rates of Cd and Re. This suggests that slow precipitation kinetics controls the accumulation of Cd and Re in these sediments. The accumulation rate of authigenic U is more variable; it may be tied to the kinetics of microbially mediated U reduction and be controlled by the availability of reactive organic matter. Authigenic Mo is distinguished by a sharp subsurface concentration minimum, above which Mo cycles with manganese. Mo released to pore water upon reduction of Mn oxides diffuses downward and enriches the subsurface sediment. Mo accumulates most rapidly in the sediment with the highest sulfide content. Slow conversion of molybdate to thiomolybdate may explain the much slower Mo accumulation rate in the less sulfidic sediments. A component of authigenic Mo accumulates with pyrite in an approximately constant Mo:Fe ratio. The accumulation rate of pyrite and associated Mo is insensitive to AVS abundance. Pyrite formation may be limited by the reactivity of iron oxide minerals.     

长江口-杭州湾毗连海区的现代沉积速率

运用沉积地层同位素210 Pb、137Cs测年技术,估算长江口 杭州湾毗连海区的现代沉积速率。研究结果表明,以泗礁水道为界,东侧的马鞍列岛区受外海高盐水的顶托,长江来沙少,淤积缓慢;西侧至长江口、杭州湾海岸交汇点 (南汇咀 )之间水域,是长江泥沙扩散南下的主要通道。其中,受长江冲淡水次级锋和杭州湾锋面输沙影响的湾口浅滩区,沉积速率约 3cm/a;洋山港区,水深大于 20m的峡道区,受强动力作用而处于侵蚀状态,峡道两端出口的浅水区,沉积速率为0.3～ 1.6cm/a;马迹山港区,位于典型的峡道沿岸淤泥质陡坡,其沉积过程不稳定,正常沉积速率为 0.7～ 3.4cm/a,但常有快速淤积和地层滑塌流失现象发生.     

Kinetics of nutrient and metal release from decomposing lake sediments

Rates of anaerobic decomposition of Lake Erie sediments were determined for seven depth intervals at three temperatures. Sealed sediment sections were incubated under anoxic conditions and the interstitial waters were serially sampled over a period of approximately 200 days. Concentration increases of bicarbonate, phosphate, ammonium, Ca, Mg, Fe and Mn in pore water within any given depth interval followed zero order kinetics over the sampling period and exhibited Arrhenius temperature dependency. Rates of release to the pore waters were proportional to the concentrations in the solid phases, indicating first order kinetics overall.The rates and temperature dependencies of these fermentation reactions were only slightly less than those reported from sediments undergoing sulfate reduction. The observed release rates decreased exponentially with depth in the sediment due to a corresponding decrease in the amount of metabolizable organic matter and acid hydrolyzable mineral phases.A stoichiometric model was constructed utilizing the observed release rates and assumed chemical reactions to predict the stoichiometry of the decomposing organic matter and the nature of the hydrogen buffer. The modeling indicates that 60% of the observed bicarbonate release is the direct result of organic decomposition, that 20% of the release is from the dissolution of calcium carbonate mineral phases, and that the remaining 20% of the release is from the dissolution of magnesium, iron und manganese carbonate mineral phases.Kinetic modeling of the observed production rates accurately predicts the vertical profiles of Ca, Mg, Fe and Mn, but cannot quantitatively account for all the concentration differences of the nutrient elements C, N and P. This implies that in addition to decomposition, increased depositional flux also accounts for the significant changes in concentrations of the nutrient elements in the near surface sediments.     

Erosion rates on different timescales derived from cosmogenic 10Be and river loads: implications for landscape evolution in the Rhenish Massif, Germany

We determined erosion rates on timescales of 10¹–10⁴ years for two catchments in the northeastern Rhenish Massif, in order to unravel the Quaternary landscape evolution in a Variscan mountain range typical of central Europe. Spatially averaged erosion rates derived from in situ produced ¹⁰Be concentrations in stream sediment of the Aabach and M?hne watersheds range from 47 ± 6 to 65 ± 14 mm/ka and integrate over the last 9–13 ka. These erosion rates are similar to local rates of river incision and rock uplift in the Quaternary and to average denudation rates since the Mesozoic derived from fission track data. This suggests that rock uplift is balanced by denudation, i.e., the landscape is in a steady state. Short-term erosion rates were derived from suspended and dissolved river loads subsequent to (1) correcting for atmospheric and anthropogenic inputs, (2) establishing calibration curves that relate the amount of suspended load to discharge, and (3) estimating the amount of bedload. The resulting solid mass fluxes (suspended and bedload) agree with those derived from the sediment volume trapped in three reservoirs. However, resulting geogenic short-term erosion rates range from 9 to 25 mm/ka and are only about one-third of the rates derived from ¹⁰Be. Model simulations in combination with published sediment yield data suggest that this discrepancy is caused by at least three factors: (1) phases with higher precipitation and/or lower evapotranspiration, (2) rare flood events not captured in the short-term records, and (3) prolonged periods of climatic deterioration with increased erosion and sediment transport on hillslopes.     

Diagenetic metal profiles in recent sediments of a scottish freshwater Loch

Integrated total elemental, phase-specific, and pore-water analyses of sediment cores from Loch Ba, Scotland, show that early diagenetic processes have promoted extensive metal enrichment immediately beneath the sediment-water interface. The accumulation of Mn, Pb, Zn, Cu, and Co in sedimentary solids upward of 3 cm depth is accompanied by an increasing residence of these elements in adsorbed and hydrous oxide phases. Such phases are formed through oxidative precipitation from the interstitial pore fluids, following the upward migration of metals from more deeply buried, anaerobic sectors of the sediment pile. There is good evidence that Fe and Ni are subject to similar influences, although their total abundances near the sediment surface are less conspicuously modified. In the Loch Ba sediments, the oxic conditions promoting metal precipitation are entirely confined to strata of postindustrial age. In the absence of fully diagnostic pore-water and sequential chemical data, similar diagenetic profiles could plausibly be misinterpreted as the product of anthropogenic contamination.     

The surface chemistry of sediments from the Panama Basin: The influence of Mn oxides on metal adsorption

The solid Mn content of sediments at a site in the Panama Basin (5°21′N 81°56′W) decreases from 3.9% in the interfacial sediment to 1% at 1.5 cm and <0.2% below 5 cm. These conditions provide an opportunity to examine the influence of Mn oxides on the metal adsorption characteristics of natural marine sediments.The adsorption of 14 metals on interfacial sediment and sediment from depths of 0.5 to 3 cm and 15 to 19 cm from the Panama Basin site was studied, and distribution coefficients (K_D) were determined. A comparison of the K_D values for a variety of samples containing different Mn contents (i.e., Panama Basin sediments, MANOP site H interfacial sediment, red clay, and buserite) indicates that an increase in the solid Mn content enhances the ability of the particles to bind certain metals (e.g., Zn, Pb, Co, Cd, and Ba) while the binding ability for other metals (e.g., Cs, Be, Sc, Pu, Sn, and Fe) is not significantly affected. For the Panama Basin sediment, the K_D values for Ni, Co, Cd, Ba, and Mn for the Mn enriched interfacial sediment are 5 to 23 times greater than the K_D values for the Mn depleted deep sediment. The K_D values for Cs, Be, Sc, Pu, and Fe for the two types of sediment are essentially the same. The correlation between the Mn content and the binding ability of the sediment for particular metals coincides with the Mn-metal correlations observed in bulk compositional data for ferromanganese nodules and sediments. This implies that the observed metal enrichments in nodules or hemipelagic sediments are most likely caused by preferential adsorption of the metals by Mn enriched phases.     

Petrology of recent caliche pisolites, spherulites, and speleothem deposits from central Texas

Recent caliche, including nodules, pisolites, crusts, internal sediment, speleothem deposits, and spherulites, has formed within the dolomitic Cretaceous Edwards Formation of central Texas. As weathering altered the host strata, rhombic crystals of calcite were precipitated concomitantly with dissolution of the dolomite, thereby forming nodules. The highly altered dolomite (i.e. pulverulite) was then removed and spar, internal sediment, and travertine accumulated in the internodular voids. Nodular masses of calcite and dolomite are the most prominent constituent of the caliche. Some of the nodules have a well developed concentric structure as well as other characteristics similar to hypersaline pisolites. Features which appear to be useful in distinguishing caliche from hypersaline pisolites are: regional geological setting, association with other caliche and palaeosoil deposits, types of fossils present, and the presence of rhombic calcite and/or bladed sparry calcite with triangular shaped cross-section. A brick-like calcite texture and relict aragonite rays characterize hypersaline pisolites. Incipient neomorphism of the nodules and pisolites has resulted in the development of a radial pattern of spar within these structures. Geopetal deposits of internal sediment, including terra rossa soil, inhibited spar growth in the upward direction; consequently, spar is much better developed on the undersides of pisolites. Crusts and travertine flowstone (speleothem) deposits are intimately associated with the nodular masses and internal sediment. The brecciated thin crusts and travertine flowstone are end products of the same processes. The crusts formed during times of periodic desiccation of the growing surface while the flowstone formed when water was relatively abundant. Spherulitic bodies within the caliche, commonly 1–2 mm in diameter, display a radial texture and yet are composed of single crystals of calcite. The structures are the product of neomorphosed Microcodium or Microcodium-like globular bodies.     

Pesticides associated with suspended sediemnts entering San Francisco Bay following the first major storm of water year 1996

Estuaries receive large quantities of suspended sediments following the first major storm of the water year. The first-flush events transport the majority of suspended sediments in any given year, and because of their relative freshness in the hydrologic system, these sediments may carry a significant amount of the sediment-associated pesticide load transported into estuaries. To characterize sediment-associated pesticides during a first-flush event, water and suspended sediment samples were collected at the head of the San Francisco Bay during the peak in suspended sediment concentration that followed the first major storm of the 1996 hydrologic year. Samples were analyzed for a variety of parameters as well as 19 pesticides and degradation products that span a wide range of hydrophobicity. Tidal mixing at the head of the estuary mixed relatively fresh suspended sediment transported down the rivers with suspended sediments in estuary waters. Segregation of the samples into groups with similar degrees of mixing between river and estuary water revealed that transport of suspended sediments from the Sacramento-San Joaquin drainage basin strongly influenced the concentration and distribution of sediment-associated pesticides entering the San Francisco Bay. The less-mixed suspended sediment contained a different distribution of pesticides than the sediments exposed to greater mixing. Temporal trends were evident in pesticide content after samples were segregated according to mixing history. These results indicate sampling strategies that collect at a low frequency or do not compare samples with similar mixing histories will not elucidate basin processes. Despite the considerable influence of mixing, a large number of pesticides were found associated with the suspended sediments. Few pesticides were found in the concurrent water samples and in concentrations much lower than predicted from equilibrium partitioning between the aqueous and sedimentary phases. The observed sediment-associated pesticide concentrations may reflect disequilibria between sedimentary and aqueous phases resulting from long equilibration times at locations where pesticides were applied, and relatively short transit times over which re-equilibration may occur.     

Zoned minerals in garnet peridotite nodules from the Colorado Plateau: implications for mantle metasomatism and kinetics

Some garnet peridotite nodules from The Thumb, a minette neck on the Colorado Plateau in the southwestern United States, contain zoned minerals. Zoning does not exceed 1.5 wt.% for any oxide, but some relative changes are large: in one garnet TiO₂ and Cr₂O₃ ranges are 0.05–0.65 and 3.5–5.0 wt.%, respectively. In two porphyroclastic nodules, garnet rims are depleted in Mg and enriched in Fe, Ti, and Na compared to cores, and one garnet is irregularly zoned in Ti and Cr. Olivine crystals in these rocks are unzoned, and pyroxene zoning is slight, yet matrix olivine and pyroxene contain more Fe and Ti and less Mg and Cr than inclusions of these phases in garnet. In three coarse nodules, garnet rims are Ti-rich compared to cores, and Ca, Fe, Mg, and Cr zoning patterns are complex. Several nodules appear to have partially equilibrated near 1200° C and 35 kb, and under these conditions cation mobility in pyroxene was greater than in garnet. The zoning partly reflects Fe and Ti metasomatism in the mantle. Calculations indicate that Fe-Mg gradients in garnet could have persisted for only a short time in the mantle, perhaps thousands of years or less, so the metasomatism occurred shortly before eruption. The minette host, a likely source of the Fe and Ti, is rich in light rare earth elements: since the nodules are much poorer in these elements, little or no infiltrated minette was trapped in them. Diffusion is a possible mechanism for nodule metasomatism. Some fertile peridotite nodules from kimberlites may have been affected by similar events. Compositional differences between inclusions in garnet and matrix phases are intriguingly similar to some of the differences between most peridotite inclusions in diamonds and common lherzolite phases.     

Biogeochemical consequences of macrofauna burrow ventilation

The burrow walls created by macrofauna in aquatic sediments are sites of intense chemical mass transfer. Quantitative measurement of their significance is, however, difficult because chemistry in the immediate vicinity of burrow walls is temporally dynamic due to periodic ventilation of burrows by macrofauna. A temporally dynamic, 2D multicomponent diffusion-reaction model was utilized to depict the magnitude and time dependency of chemical mass transfer in the immediate vicinity of burrow walls as well as at the water/sediment interface. The simulation results illustrate that sediment particles, pore water, and microorganisms within a few millimeters of burrow walls experience significant oscillation in pH (as much as two pH units) and dissolved oxygen concentration (between saturation and near anoxia) whereas such oscillation is absent at the water/ sediment interface. The geochemical oscillation is expected to affect the net stability of mineral phases, activities and community structures of microorganisms, and rates and magnitudes of microbial diagenetic reactions.     

Sediment Accumulation Rates and Submersed Aquatic Vegetation (SAV) Distributions in the Mesohaline Chesapeake Bay, USA

This study assesses spatial and temporal sedimentological trends in four mesohaline Chesapeake Bay submersed aquatic vegetation (SAV) habitats, two with persistent SAV beds and two with ephemeral SAV beds, to determine their relationship to current and historical sediment characteristics??grain size, organic content, and accumulation rates. In general, grain size is similar among all sites, and subsurface sediment differs from surficial sediment only at one site where a thin surficial sand layer (??2?C3?cm) is present. This thin sand layer is not completely preserved in the longer-term sedimentary record even though it is critical to determining whether the sediment is suitable for SAV. Evidence for nearshore fining, similar to that observed in the deeper waters of the Bay, is present at the site where the shoreline has been hardened suggesting that locations with hardened shorelines limit exchange of coarser (sandy) material between the shore and nearshore environments. Whether the fining trend will continue to a point at which the sediment will become unsuitable for SAV in the future or whether some new type of equilibrium will be reached cannot be addressed with our data. Instead, our data suggest that SAV presence/absence is related to changes in sedimentary characteristics??persistent beds have relatively steady sediment composition, while ephemeral beds have finer sediments due to reduced sand input. Additionally, sediment accumulation rates in the persistent beds are ??9?mm/year, whereas rates in the ephemeral beds are ??3?mm/year. Thus, the ephemeral sites highlight two potential sedimentary controls on SAV distribution: the presence of a sufficiently thick surficial sand layer as previously postulated by Wicks (2005) and accumulation rates high enough to bury seeds prior to germination and/or keep up with sea-level rise.     

Site preservation along an active meandering and avulsing river: The Red River,Arkansas

The low-gradient Red River is a rapidly migrating, sinuous stream with easily erodible banks. Avulsion is common at many scales, from individual meander bends that are cut off to major sections of the river that form multiple, complex meander belts. The present meander belt can be subdivided into mappable landforms—termed phases—that are associated with river courses of different ages and thus associated with archeological sites of different ages. Within the study area two phases are present. The younger Modern meander belt phase has formed within the past 0.2–0.3 ky, precluding preservation of prehistoric archaeological sites. Any protohistoric artifacts that may have been preserved in this meander belt phase would be deeply buried because as much as 2 m of the vertical accretion sediment has accumulated between artificial levees in <0.1 ky and 1–2 m of sediment has accumulated beyond the artificial levees in <0.2 ky. Archeological site preservation in this highly mobile fluvial end member can be used as a predictor for other, similar streams. A large prehistoric site is preserved on an older (0.5–1 kya) Late Prehistoric meander belt phase associated with an abandoned river course. In the study area a Fourche Maline 7 period (A.D. 800–900) through Caddo IV period (ca. A.D. 1500–1700) archeological site (3MI3/30) is preserved on this slightly higher altitude portion of the flood plain. At locations proximal to the river, the site may be buried by overbank sediment 0.4 m thick, but at more distant locations the site is at the surface or only buried by thin overbank sediment because of low sedimentation rates (0.04 cm yr⁻¹) over the span of a millennium. Sites, such as 3MI3/30, that are occupied contemporaneous with overbank sedimentation may be stratified; however, localized erosion and removal of some archeological material may occur where channelized flow crosses the natural levee. © 1998 John Wiley & Sons, Inc.     

Accumulation and fractionation of trace elements in soil ferromanganese nodules of different size

The concentrations and distribution of bulk and mobile species of trace elements were investigated in various size fractions of ferromanganese nodules from bleached meadow-brown soils. It was shown that the enrichment factor of trace elements increases during the growth of nodules; however, the character of element accumulation appeared to depend on the nature of the element. The nodules intensely accumulate Mn, Co, Ni, and Pb and, to a lesser extent, Cu and Mo. The process of trace element uptake by the nodules is most contrasting in the middle part of the soil profile. The nature of trace element concentration by soil nodules is rather complex and requires further special investigations.