Factors controlling regional spatial distribution of 53 elements in coastal sea sediments in northern Japan: Comparison of geochemical data derived from stream and marine sediments

In all, 53 elements were analyzed in 1406 coastal sea sediment samples collected from an area off Hokkaido and the Tohoku region of Japan during a nationwide marine geochemical mapping project. The spatial distribution patterns of the elemental concentrations in coastal seas along with the existing geochemical maps in terrestrial areas were used to define natural geochemical background variation and mass transport processes. The terrestrial area is covered by mafic volcanic rocks and accretionary complexes associated with ophiolite, which has small amounts of felsic volcanic rocks and granite. The spatial distribution patterns of elements enriched in mafic lithologies such as Fe (Total Fe₂O₃) and Sc in marine environments are influenced by adjoining terrestrial materials. The spatial distribution patterns of Cr and Ni concentrations, which are highly abundant in ultramafic rocks on land, are used to evaluate the mass transport from land to the sea and the dispersive processes caused by oceanic currents. The scale of mass transport by oceanic currents occurs up to a distance of 100–200 km from the coast along the coastal areas. The regional differences of elements rich in felsic lithologies such as K (K₂O), Nb and La in marine sediments are determined mainly by the relative proportion of minerals and lithic fragments enriching felsic materials to those associated with mafic materials. The spatial distribution of elemental concentration is not always continuous between the land areas and coastal sea areas. That difference is interpreted as resulting from (1) transportation of marine sediments by oceanic currents and storm waves, (2) contribution of volcanic materials such as tephra, (3) occurrence of shell fragments and foraminifera tests and (4) distribution of relict sediments of the last glacial age and early transgression age. Contamination with Cu, Zn, Cd, As, Mo, Sn, Sb, Hg, Pb and Bi was not observed in marine environments because the study area has little anthropogenic activity. Terrestrial materials are the dominant source for these metals. The Mo, Cd, Sn, Sb, Hg, Pb and Bi are abundant in silty and clayey sediments locally because of early diagenetic processes, authigenic precipitation and organic substances associated with these elements. The spatial distribution of As concentration shows exceptions: it is concentrated in some coarse and fine sands on the shelf. The enrichment is explained by adsorption of As, sourced from a coal field, to Fe hydroxide.     

Non-transparent uppermost mantle in the island-arc region of Japan

In Japan, the crust and uppermost mantle seismic character is yet unimaged although many refraction surveys have been recorded. The longest seismic profiles are analyzed. A remarkable feature, a long-duration coda wave after the PmP wave (reflected wave at the Moho boundary), is observed on the record sections. Several possible models are considered to explain the long-duration coda wave. The model with many scatterers located in the uppermost mantle explains the observed data well while the undulating Moho and continuous layering models do not account for some aspects of the observed data. The scatterer distributed uppermost mantle is not consistent with that of continental region which is often characterized as transparent. We estimate the scattering coefficient of the uppermost mantle and crust using simulations. The scattering coefficients obtained for upper crust, lower crust, and uppermost mantle are 0.01, 0.02, and 0.025, respectively. The scattering coefficient of the uppermost mantle is slightly larger than that of lower crust, which is characterized as being reflective. The many scatterers in the uppermost mantle might be related to magmatism in Japan. This will be one of the important observations for understanding formation processes of the Moho boundary and uppermost mantle in the island-arc environment.     

Geochemical behavior of Pt and Pd in coastal marine sediments,southeastern margin of the Japan Sea

Eighty-one argillaceous marine sediments collected from the southeastern coastal margin of the Japan Sea were analyzed for Pt and Pd by atomic absorption spectrometry using a graphite furnace atomizer after solvent extraction separation. The average Pt (1.2 ± 0.5 ppb) and Pd(1.6 ± 0.9 ppb) contents are generally similar to those of the published crustal abundances. The Pt or Pd is generally enriched in the fine sediment fraction, and positively correlated with Cu, Pb and water depth. The inverse correlation between the Pt or Pd content and redox potential of the sediment suggests that significant amounts of Pt and Pd are supplied in their dissolved forms, and reduced to their metallic states. It is concluded that the Pt and Pd distributions in the coastal marine sediments are controlled by the geological characteristics of the studied area, grain size and redox potential of sediments, water depths, and dissolved O₂ concentration of sea water.     

The pollution of marine sediments by trace elements in the coastal region of Togo caused by dumping of cadmium-rich phosphorite tailing into the sea

 The marine coastal sediments from Togo have been analysed for the trace elements Cd, Cr, Cu, Ni, Pb, Sr, V, Zn and Zr to ascertain the geo-ecological impact of dumping of phosphorite tailings into the sea. Trace element concentrations ranged from 2–44 ppm for Cd, 22–184 ppm for Cu, 19–281 ppm for Ni, 22–176 ppm for Pb, 179–643 ppm for Sr, 38–329 ppm for V, 60–632 ppm for Zn and 18–8928 ppm for Zr. Regional distribution of trace elements in the marine environment indicates that the concentrations of Cr, Cu, Ni, Pb, V, Sr and Zn increase seawards and along the coastal line outwards of the tailing outfall, whereas Cd and Zr showed reversed spatial patterns. Sorting and transport of phosphorite particles by coastal currents are the main factors controlling the distribution of particle-bound trace metals in the coastal environment. The Cd, Sr and Zn concentrations decrease with decreasing grain size in marine coastal sediments, whereas Cr, Cu, Ni and Zn concentrations increase with decreasing grain size. Percolation and shaking experiments were carried out in laboratory using raw phosphate material and artificial sea water. Enhanced mobilization of Cd from phosphorites by contact with the sea water was observed. Received: 11 May 1998 · Accepted: 20 October 1998     

Post-glacial regional climate variability along the East Antarctic coastal margin—Evidence from shallow marine and coastal terrestrial records

We review the post-glacial climate variability along the East Antarctic coastline using terrestrial and shallow marine geological records and compare these reconstructions with data from elsewhere. Nearly all East Antarctic records show a near-synchronous Early Holocene climate optimum (11.5–9 ka BP), coinciding with the deglaciation of currently ice-free regions and the optimum recorded in Antarctic ice and marine sediment cores. Shallow marine and coastal terrestrial climate anomalies appear to be out of phase after the Early Holocene warm period, and show complex regional patterns, but an overall trend of cooling in the terrestrial records. A Mid to Late Holocene warm period is present in many East Antarctic lake and shallow coastal marine records. Although there are some differences in the regional timing of this warm period, it typically occurs somewhere between 4.7 and 1 ka BP, which overlaps with a similar optimum found in Antarctic Peninsula terrestrial records. The differences in the timing of these sometimes abrupt warm events in different records and regions points to a number of mechanisms that we have yet to identify. Nearly all records show a neoglacial cooling from 2 ka BP onwards. There is no evidence along the East Antarctic coastline for an equivalent to the Northern Hemisphere Medieval Warm Period and there is only weak circumstantial evidence in a few places for a cool event crudely equivalent in time to the Northern Hemisphere's Little Ice Age. There is a need for well-dated, high resolution climate records in coastal East Antarctica and particularly in Terre Adélie, Dronning Maud Land and Enderby Land to fully understand the regional climate anomalies, the disparity between marine and terrestrial records, and to determine the significance of the heterogeneous temperature trends being measured in the Antarctic today.     

Heavy metal concentrations in sediments and in mussels from Argentinean coastal environments,South America

Among environmental contaminants, heavy metals are currently considered to be some of the most toxic ones present worldwide due to their harmful effects on organisms and ability to bioaccumulate in aquatic systems. In this work, the concentration of heavy metals (Cd, Cu, Pb, Zn, Ni and Cr) in Brachidontes rodriguezii and in the fine sediments of several coastal sites at the southwest of Buenos Aires Province, Argentina is analyzed. The Bahía Blanca Estuary and Pehuen-Có beach are located in a highly complex oceanographic and ecological regional system, which creates the basis of one of the most valuable Argentinean habitats for fishing commercial species. An assessment, which involved analyzing distribution pattern of trace metals, comparative studies with sediment and ecological quality guidelines; and a sequential and integrated index analyses approach (containing Metal Pollution Index, Biosediment Accumulation Factor, Geo-accumulation Index (Igeo), Pollution Load Index and the mean Probable Effect Level quotients), was followed to estimate enrichment and risks of heavy metals in the sediments and in the mussels from these study areas. The results showed higher concentrations of some heavy metals (e.g., Cd, Cr and Ni) in mussels collected at Pehuen-Có, while no spatial differences in sediments were observed. According to the international environmental regulations, mean values of trace metals in mussels allowed to place both sites between “unpolluted and moderately polluted” and between the “low and medium category” of pollution. Furthermore, the mean concentrations found were within the detected ranges in other coastal sites worldwide.     

Modelling ice-sheet sensitivity to late weichselian environments in the svalbard-barents sea region

Ice-proximal sedimentological features from the northwestern Barents Sea suggest that this region was covered by a grounded ice sheet during the Late Weichselian. However, there is debate as to whether these sediments were deposited by the ice sheet at its maximum or a retreating ice sheet that had covered the whole Barents Sea. To examine the likelihood of total glaciation of the Late Weichselian Barents Sea, a numerical ice-sheet model was run using a range of environmental conditions. Total glaciation of the Barents Sea, originating solely from Svalbard and the northwestern Barents Sea, was not predicted even under extreme environmental conditions. Therefore, if the Barents Sea was completely covered by a grounded Late Weichselian ice sheet, then a mechanism (not accounted for within the glaciological model) by which grounded ice could have formed rapidly within the central Barents Sea, may have been active during the last glaciation. Such mechanisms include (i) grounded ice migration from nearby ice sheets in Scandinavia and the central Barents Sea, (ii) the processes of sea-ice-induced ice-shelf thickening and (iii) isostatic uplift of the central Barents Sea floor.     

Determination of organochlorine compounds in coastal marine sediments from the southern west of the Mediterranean Sea

Recent evidence suggests that polychlorinated biphenyls might also have adverse reproductive, developmental and endocrine effects. Although, the use of polychlorobiphenyls in Algeria has been banned for more than two decades, large quantities of these compounds containing products remain disseminated, mainly stored in obsolete or damaged equipments. This research describes a study to assess polychlorinated biphenyls distribution in marine sediments collected from the seaside of Tamentfoust touristic resort located in the eastern side of Algiers Bay. After microwave-assisted extraction and purification with both concentrated sulphuric acid and activated silica gel, the extracts were analyzed by gas chromatography with an electron capture detector. Relatively high contamination levels of polychlorinated biphenyls were found in samples collected from the port of Tamentfoust (15 to 70 ng/g d.w.), while the concentrations were lower in the stations located outside the port (0 to 26 ng/g d.w.). Compared with data previously reported by some other researchers, the polychlorobiphenyls concentrations found in this work showed an environmental persistence, but a decrease of approximately 5 times in 30 year i.e since the ban of the use of polychlorinated biphenyls. The predominant polychlorinated biphenyls congeners in all sediment samples were polychlorinated biphenyls138, 153, 180 and 187. This composition was similar to industrial mixture (Aroclor 1260). This probably indicated that the contamination originated from the port and has a continental source.     

Compositional similarities of non-solvent extractable fatty acids from recent marine sediments deposited in differing environments

Five recent sediment samples from a variety of North American continental shelves were analyzed for fatty acids (FAs) in the solvent-extractable (SOLEX) lipids as well as four types of non-solvent extractable (NONEX) lipids. The NONEX lipids were operationally defined by the succession of extraction procedure required to recover them. The complete procedure included (i) very mild acid treatment, (ii) HF digestion and (iii) saponification of the sediment residue following exhaustive solvent extraction.The distribution pattern and various compositional parameters of SOLEX FAs in the five sediments were divided into three different groups, indicating the difference of biological sources and also diagenetic factors and processes among the three groups of samples. Nevertheless, the compositions of the corresponding NONEX FAs after acid treatment were surprisingly very similar. This was also true for the remaining NONEX FA groups in the five sediment samples.The findings implied that most of the NONEX FAs reported here are derived directly from living organisms. It is also concluded that a large part of NONEX FAs are much more resistant to biodegradation than we have thought, so that they can form the large percentage of total lipids with increasing depth of water and sediments.     

The occurrence and distribution of tin with particular reference to marine environments

Concentrations of tin in sea water decreased from estuarine and shelf (0.02-0.04 μg/kg) to surface Atlantic waters (0.009 μg/kg). Mean contents (ppm) in other materials included: ultramafic rocks, 0.8; basalts, 1.7; silicic rocks, 2.5; red clays, 3.4; amphibolites, 1.2. Oceanic ferromanganese deposits contained from 0.2 to 5.8 ppm; tin and cobalt contents were correlated.     

Distribution of trace elements in the coastal sea sediments of Maslinica Bay, Croatia

Spatial distributions of trace elements in the coastal sea sediments and water of Maslinica Bay (Southern Adriatic), Croatia and possible changes in marine flora and foraminifera communities due to pollution were investigated. Macro, micro and trace elements’ distributions in five granulometric fractions were determined for each sediment sample. Bulk sediment samples were also subjected to leaching tests. Elemental concentrations in sediments, sediment extracts and seawater were measured by source excited energy dispersive X-ray fluorescence (EDXRF). Concentrations of the elements Cr, Cu, Zn, and Pb in bulk sediment samples taken in the Maslinica Bay were from 2.1 to over six times enriched when compared with the background level determined for coarse grained carbonate sediments. A low degree of trace elements leaching determined for bulk sediments pointed to strong bonding of trace elements to sediment mineral phases. The analyses of marine flora pointed to higher eutrophication, which disturbs the balance between communities and natural habitats.     

Modeling of subsurface calcite dissolution, including the respiration and reoxidation processes of marine sediments in the region of equatorial upwelling off Gabon

Mineralization of organic matter and the subsequent dissolution of calcite were simulated for surface sediments of the upper continental slope off Gabon by using microsensors to measure O₂, pH, pCO₂ and Ca²⁺ (in situ), pore-water concentration profiles of NO₃⁻, NH₄⁺, Fe²⁺, and Mn²⁺ and SO₄²⁻ (ex situ), as well as sulfate reduction rates derived from incubation experiments. The transport and reaction model CoTReM was used to simulate the degradation of organic matter by O₂, NO₃⁻, Fe(OH)₃ and SO₄²⁻, reoxidation reactions involving Fe²⁺ and Mn²⁺, and precipitation of FeS. Model application revealed an overall rate of organic matter mineralization amounting to 50 μmol C cm⁻² yr⁻¹, of which 77% were due to O₂, 17% to NO₃⁻ and 3% to Fe(OH)₃ and 3% to SO₄²⁻. The best fit for the pH profile was achieved by adapting three different dissolution rate constants of calcite ranging between 0.01 and 0.5% d⁻¹ and accounting for different calcite phases in the sediment. A reaction order of 4.5 was assumed in the kinetic rate law. A CaCO₃ flux to the sediment was estimated to occur at a rate of 42 g m⁻² yr⁻¹ in the area of equatorial upwelling. The model predicts a redissolution flux of calcite amounting to 36 g m⁻² yr⁻¹, thus indicating that ∼90% of the calcite flux to the sediment is redissolved.     

Magnetic studies applied to different environments (soils and stream sediments) from a relatively polluted area in Buenos Aires Province,Argentina

Anthropogenic influence, mainly due to urban and industrial activities, may affect fluvial environments and soils, via atmospheric contamination and liquid and solid waste.Continuing previous works on stream sediments and soils, the Gran La Plata area was chosen. In this area, located in the Northeast of Buenos Aires Province (Argentina), several streams and soils were sampled. The streams have similar characteristics, although some of them have a higher input of pollutants (fluvial effluents, fly ashes, solid wastes, etc.). The studied soils have different pedological development.Magnetic and chemical studies were carried out in the laboratory. Analyses of the results indicated that the behavior of magnetic parameters can be related to the variations of heavy metal contents in stream sediments but there is not a good correlation in soils. The comparison between both environments (stream-sediment and soils) reveals a different impact of pollutants. Magnetite, especially PSD grains, seems to be the main carrier for both environments.     

A theoretical model of the stable sulfur isotope distribution in marine sediments

A diffusion-diagenesis model of the sulfur cycle is developed to calculate theoretical distributions of stable sulfur isotopes in marine sediments. The model describes the depth variation in δ³⁴S of dissolved sulfate and H₂S. and of pyrite. The effects of sulfate reduction, sulfate and H₂S diffusion. and of sedimentation are considered as well as the bacterial isotope fractionation and the degree of pyrite formation. Under open system conditions of sulfur diagenesis the isotopic difference, ΔSO^2?₄ — H₂S, tends to increase with depth being smaller than the bacterial fractionation factor near the sediment surface and larger in deeper layers. The two isotopes in SO^2?₄ or in H₂S do not diffuse in the same proportion as they occur in the porewater. This explains why sulfur, which is incorporated from seawater sulfate by diffusion and precipitation as pyrite, can be enriched in ³²S relative to the seawater sulfate. The model calculations demonstrate the importance of taking the whole dynamic sulfur cycle into account before drawing conclusions about sulfur diagenesis from the stable isotope distribution.     

Mobilisation of traffic-derived trace metals from road corridors into coastal stream and estuarine sediments,Cairns, northern Australia

This investigation revealed the presence of traffic-derived metals within road, stream and estuarine sediments collected from a coastal catchment, northern Australia. Studied road sediments displayed variable total metal concentrations (median Cd, Cu, Pb, Pd, Pt, Ni and Zn values: 0.19, 42.6, 67.5, 0.064, 0.104, 36.7 and 698 mg/kg, respectively). The distinctly elevated Zn values are due to abundant tyre rubber shreds (as verified by SEM-EDS and correlation analysis). By comparison to the road sediments, background stream sediments taken upstream from roads have relatively low median Pb, Pd, Pt and Zn concentrations (7.3 mg/kg Pb, 0.01 mg/kg Pd, 0.012 mg/kg Pt, 62 mg/kg Zn). Stream and estuarine sediment samples collected below roads have median values of 21.8 mg/kg Pb, 0.014 mg/kg Pd, 0.021 mg/kg Pt and 71 mg/kg Zn, and exhibit ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb ratios that appear on a mixing line between the isotopically distinct background stream sediments and the road sediments. Thus, mobilisation of dusts and sediments from road surfaces has resulted in relatively elevated Pb, Pd, Pt and Zn concentrations and non-radiogenic Pb isotope ratios in local coastal stream and estuarine sediments. The investigation demonstrates that traffic-derived metals enter coastal stream and estuary sediments at the fringe of the Great Barrier Reef lagoon.     

Calcium distribution in soils and stream sediments in Istria (Croatia) and the Slovenian littoral

For experimental geochemical mapping soil was sampled in 5×5 km regular grid in Istria and the Slovenian littoral (Croatia and Slovenia). The territory consists predominantly of karstified limestones and dolomites, and of flysch beds exposed in two basins, Istrian and Brkini. In addition to soil, stream sediment was also collected in the flysh area. Sampling was performed according to an analysis of variance design that permitted one to estimate the effects of the sample medium, geographic position, sampling error and analytical error. The analysis of variance of chemical variables indicated that soil and stream sediment as sampling media lead to similar results in producing geochemical maps. The largest differences with respect to the lithologic substrate of soil is indicated by calcium. As shown by the geochemical map, calcium in soil is high on the Istrian flysch beds, and low on limestones as well as on the flysch beds of the Brkini basin. The two soils also differ in mineralogy. The reason for this difference seems to lie in soil genesis on limestone and on flysch, and in the variable calcium content of flysch beds. The results of Q-mode factor analysis confirmed the adherence of soil and stream sediment of the two flysch basins to two differing groups. This difference was discovered by geochemical mapping. The hypothesis of differing calcium content in the rocks of the two basins was confirmed by the investigation of fresh and weathered rocks and soils in eight profiles sampled in the Brkini and Istrian flysch basin. It was found that the sandstone and calcarenitic samples from the Istrian basin contain an average factor of 3.5 more Ca than those of the investigated Brkini basin, and the samples of Istrian marls 4 times more Ca than those of the Brkini siltstones. Furthermore, the investigated weathered rocks and soils that originated from these rocks in the Istrian basin contain considerably more Ca than in the Brkini basin. In comparison with sandstone and siltstone samples of the Brkini basin, sandstone, calcarenite and marl samples of the Istrian flysch basin contain less clay minerals, quartz and feldspars and more calcite.