Sediment transport,biotic modifications and selection of grain size in a surface deposit-feeder

Deposit-feeders often select for particles on the basis of grain size. The available pool of particles at the sediment surface may be modified both by deposit-feeder activity and by sediment transport, but the effects of these alterations on deposit-feeder diet composition have received little attention. In laboratory experiments the spionid polychaeteParaprionospio pinnata altered the grain-size composition in its foraging area, and these alterations were reflected in grain-size changes in the diet. After simulated transport of fine-grain sediments,P. pinnata diets also changed in grain-size composition. Field data were collected from 9 m depth in the lower Chesapeake Bay. A video camera, deployed near the bottom, identified times of sediment transport over a 6-h Period;P. pinnata were collected concurrently for gut analysis. Consistent with predictions from the laboratory experiments,P. pinnata ingested primarily small-grain sizes. During periods of no sediment transport this feeding pattern reduced the relative availability of small particles; larger sediments were incorporated into the diet. Sediment transport may resupply the foraging area with fine-grain particles which are then incorporated into the diet. On these small spatial and time scales, deposit-feeder activity may affect the availability of food resources.     

Variations in the content and distribution of n-alkanes in a series of carboniferous vitrinites and sporinites of bituminous rank

n-Alkanes in the soluble organic matter extracted from a series of vitrinite and sporinite concentrates have been analysed by gas chromatography. The macerals were isolated from coals ranging in rank from 77.1% to 86.6% carbon (vitrinite: dry, ash-free), and yields of n-alkanes ranged from 10 to 580 ppm for vitrinites and from 20 to 970 ppm for sporinites. The maximum yields were found at a rank of 85.4% C from vitrinites and 86.6% C from sporinites.Distribution maxima of the n-alkanes, as shown by gas chromatography, range from C₂₇ and C₂₉ at lower ranks to as low as C₁₆ at higher ranks. The distributions also show a progressive decrease in the preference of odd-carbon-number homologues with increasing rank. Virtually smooth distributions were attained in high-volatile bituminous A coals. Quantitative data show that the loss of the odd-carbon-number preference occurred, for the most part, while individual long-chain homologues increased in concentration.There is a progressive increase in the amounts of shorter-chain n-alkanes with increasing rank. It is suggested that sequential processes may have occurred whereby the rate of formation of long-chain n-alkanes in high-volatile bituminous A rank macerals becomes slower than their rate of subsequent fragmentation to shorter chain lengths. Consequently, assuming derivation from the insoluble maceral matrices, the chain-length distributions of parent n-alkyl structures within the insoluble material may retain characteristics pertaining more to the nature of the source organic matter at the time of deposition than do the extractable n-alkane patterns, especially at higher ranks.     

The typing of Au and base-metal occurrences by plasma/mass spectrometry: initial results

This paper discusses the application of the newly developed ELAN 250 I.C.P./mass spectrometer to exploration geochemistry. This instrument combines an inductively coupled plasma with a quadrupole mass spectrometer. The combination of these two existing technologies makes it possible for the first time to perform stable-isotope and elemental analysis rapidly and concurrently.Particular attention is paid to the use of lead isotopes to type Au and base-metal occurrences. Data are presented on galena samples obtained from the Geological Survey of Canada and the Royal Ontario Museum. Consideration is also given to the potential usefulness of Pb isotopes and trace-element data to type mineral occurrences and to identify new ones.     

Long-term monitoring of the behavior of a talus-colluvium deposit

Landslides - This article describes the behavior of a talus-colluvium deposit up to 70-m thick located in the Serra dos Orgaos, Rio de Janeiro/RJ, Brazil. The monitoring dataset of 13 years...     

Biogeochemical Zones Within a Macrotidal,Dry-Tropical Fluvial-Marine Transition Area: A Dry-Season Perspective

The Fitzroy River delivers large amounts of nutrients and fine sediments to Keppel Bay (contiguous with the Great Barrier Reef Lagoon) during intermittent flow events. This study explores sources, forms and transformations of nutrients in Keppel Bay, and develops a functional process zonation that integrates seabed geochemistry and water column nutrient characteristics which are controlled by suspended sediment. The water column and seabed properties were investigated over two dry seasons, with supplementary core incubations taken to measure carbon decomposition rates and nutrient fluxes. Keppel Bay can be divided into three zones, the: zone of maximum resuspension (ZMR); coastal transitional zone (CTZ); and blue water zone (BWZ). Mineralisation of predominantly terrestrial organic matter occurs in the ZMR where nutrient uptake by phytoplankton is light limited. The CTZ and BWZ had higher light penetration and phytoplankton growth was likely limited by N and P, respectively. The identified zones conform to the bathymetry and hydrodynamic characteristics of the bay, allowing for the development of an integrated conceptual model accounting for the benthic and pelagic biogeochemical processes. Recognition of these different zones shows that considerable variation in benthic and water column properties is possible within a small system with the bathymetric and hydrodynamic characteristics of the fluidized bed reactor.     

Grinding of mineral mixtures in high-pressure grinding rolls

Attempts at improving comminution machines generally have been directed towards increasing the performance efficiency, particularly increasing throughput rate and decreasing energy consumption. The latest and most successful new comminution technology has been the high-pressure grinding rolls (HPGR), which have proved to be highly efficient in energy consumption and to have a relatively high throughput rate at low steel consumption. Already used extensively in cement plants worldwide, the first HPGRs in the mineral industry were installed in plants processing diamond ores. They are now finding their way into the large-scale base-metal mining industry. Since feed constituents in natural ores vary in their physical properties such as hardness, plasticity and brittleness, the present paper is concerned with an investigation of the behavior of a heterogeneous feed as it passes through the HPGR. The effect of feed composition on operational parameters, the energy efficiency of comminution, and energy distribution among the feed components is addressed. Mineral particles with high hardness act as energy transfer agents in the roll gap and enhance the grinding of softer mineral particles in a mixed feed.     

Mathematical models for petroleum-forming processes: n-paraffins and isoprenoid hydrocarbons

Mathematical models have been developed which simulate both random and nonrandom thermal cracking of branched and straight-chain hydrocarbons. Application of these models to n-paraffins suggests that thermal cracking alone cannot be the dominant mechanism in formation of the n-paraffin distributions present in crude oils. Application to isoprenoid hydrocarbons indicates that nonrandom cracking could be important in producing the isoprenoid distributions found in oils.Results of the mathematical modeling show that methane formation should, as predicted from energy considerations, be kinetically disfavored. It therefore is likely that substantial quantities of methane are produced from saturated hydrocarbons only under thermal conditions more severe than those under which oil is produced.The mathematical models employed are adaptable for other geochemical applications, such as isotope fractionation.     

Effect of adsorbed metal ions on the transport of Zn- and Ni-EDTA complexes in a sand and gravel aquifer

Adsorption, complexation, and dissolution reactions strongly influenced the transport of metal ions complexed with ethylenediaminetetraacetic acid (EDTA) in a predominantly quartz-sand aquifer during two tracer tests conducted under mildly reducing conditions at pH 5.8 to 6.1. In tracer test M89, EDTA complexes of zinc (Zn) and nickel (Ni), along with excess free EDTA, were injected such that the lower portion of the tracer cloud traveled through a region with adsorbed manganese (Mn) and the upper portion of the tracer cloud traveled through a region with adsorbed Zn. In tracer test S89, Ni- and Zn-EDTA complexes, along with excess EDTA complexed with calcium (Ca), were injected into a region with adsorbed Mn. The only discernable chemical reaction between Ni-EDTA and the sediments was a small degree of reversible adsorption leading to minor retardation. In the absence of adsorbed Zn, the injected Zn was displaced from EDTA complexes by iron(III) [Fe(III)] dissolved from the sediments. Displacement of Zn by Fe(III) on EDTA became increasingly thermodynamically favorable with decreasing total EDTA concentration. The reaction was slow compared to the time-scale of transport. Free EDTA rapidly dissolved aluminum (Al) from the sediments, which was subsequently displaced slowly by Fe. In the portion of tracer cloud M89 that traveled through the region contaminated with adsorbed Zn, little displacement of Zn complexed with EDTA was observed, and Al was rapidly displaced from EDTA by Zn desorbed from the sediments, in agreement with equilibrium calculations. In tracer test S89, desorption of Mn dominated over the more thermodynamically favorable dissolution of Al oxyhydroxides. Comparison with results from M89 suggests that dissolution of Al oxyhydroxides in coatings on these sediment grains by Ca-EDTA was rate-limited whereas that by free EDTA reached equilibrium on the time-scale of transport. Rates of desorption are much faster than rates of dissolution of Fe oxyhydroxides from sediment-grain surfaces and, therefore, adsorbed metal ions can strongly influence the speciation of ligands like EDTA in soils and sediments, especially over small temporal and spatial scales.