Coastal erosion vs riverine sediment discharge in the Arctic Shelf seas

This article presents a comparison of sediment input by rivers and by coastal erosion into both the Laptev Sea and the Canadian Beaufort Sea (CBS). New data on coastal erosion in the Laptev Sea, which are based on field measurements and remote sensing information, and existing data on coastal erosion in the CBS as well as riverine sediment discharge into both the Laptev Sea and the CBS are included. Strong regional differences in the percentages of coastal erosion and riverine sediment supply are observed. The CBS is dominated by the riverine sediment discharge (64.45᎒⁶ t a^-1) mainly of the Mackenzie River, which is the largest single source of sediments in the Arctic. Riverine sediment discharge into the Laptev Sea amounts to 24.10᎒⁶ t a^-1, more than 70% of which are related to the Lena River. In comparison with the CBS, the Laptev Sea coast on average delivers approximately twice as much sediment mass per kilometer, a result of higher erosion rates due to higher cliffs and seasonal ice melting. In the Laptev Sea sediment input by coastal erosion (58.4᎒⁶ t a^-1) is therefore more important than in the CBS and the ratio between riverine and coastal sediment input amounts to 0.4. Coastal erosion supplying 5.6᎒⁶ t a^-1 is less significant for the sediment budget of the CBS where riverine sediment discharge exceeds coastal sediment input by a factor of ca. 10.     

Sustainability of a Tidal Freshwater Marsh Exposed to a Long-term Hydrologic Barrier and Sea Level Rise

A 115-year-old railroad levee bisecting a tidal freshwater marsh perpendicular to the Patuxent River (Maryland) channel has created a northern, upstream marsh and a southern, downstream marsh. The main purpose of this study was to determine how this levee may affect the ability of the marsh system to gain elevation and to determine the levee’s impact on the marsh’s long-term sustainability to local relative sea level rise (RSLR). Previously unpublished data from 1989 to 1992 showed that suspended solids and short-term sediment deposition were greater in the south marsh compared to the north marsh; wetland surface elevation change data (1999 to 2009) showed significantly higher elevation gain in the south marsh compared to the north (6?±?2 vs. 0?±?2 mm year^?1, respectively). However, marsh surface accretion (2007 to 2009) showed no significant differences between north and south marshes (23?±?8 and 26?±?7 mm year^?1, respectively), and showed that shallow subsidence was an important process in both marshes. A strong seasonal effect was evident for both accretion and elevation change, with significant gains during the growing season and elevation loss during the non-growing season. Sediment transport, deposition and accretion decreased along the intertidal gradient, although no clear patterns in elevation change were recorded. Given the range in local RSLR rates in the Chesapeake Bay (2.9 to 5.8 mm year^?1), only the south marsh is keeping pace with sea level at the present time. Although one would expect the north marsh to benefit from high accretion of abundant riverine sediments, these results suggest that long-term elevation gain is a more nuanced process involving more than riverine sediments. Overall, other factors such as infrequent episodic coastal events may be important in allowing the south marsh to keep pace with sea level rise. Finally, caution should be exercised when using data sets spanning only a couple of years to estimate wetland sustainability as they may not be representative of long-term cumulative effects. Two years of data do not seem to be enough to establish long-term elevation change rates at Jug Bay, but instead a decadal time frame is more appropriate.     

Distributions of pesticides and organic contaminants between water and suspended sediment,San Francisco Bay,California

Suspended-sediment and water samples were collected from San Francisco Bay in 1991 during low river discharge and after spring rains. All samples were analyzed for organophosphate, carbamate, and organochlorine pesticides; petroleum hydrocarbons; biomarkers; and polynuclear aromatic hydrocarbons. The objectives were to determine the concentrations of these contaminants in water and suspended sediment during two different hydrologic conditions and to determine partition coefficients of the contaminants between water and sediment. Concentrations of hydrophobic contaminants, such as polynuclear aromatic hydrocarbons, varied with location of sample collection, riverine discharge, and tidal cycle. Concentrations of hydrophobic contaminants in suspended sediments were highest during low river discharge but became diluted as agricultural soils entered the bay after spring rains. Polynuclear aromatic hydrocarbons defined as dissolved in the water column were not detected. The concentrations sorbed on suspended sediments were variable and were dependent on sediment transport patterns in the bay. In contrast, the relatively hydrophilic organophosphate pesticides, such as chlorpyrifos and diazinon, has a more uniform concentration in suspended sediment. These pesticides were detected only after spring rains. Most of the measured diazinon, at least 98% for all samples, was in the dissolved phase. Measured partition coefficients for diazinon generally were uniform, which suggests that suspended-sediment concentrations were close to equilibrium with dissolved concentrations. The concentration of diazinon sorbed to suspended sediments, at any given sampling site, was driven primarily by the more abundant solution concentration. The concentrations of diazinon sorbed to suspended sediments, therefore, were independent of the patterns of sediment movement.     

Potential effect of natural radionuclides in riverbed sediments: a statistical approach based on granulometric and magnetic mineral differences

South India is one of the regions in the world that has the highest background radiation levels. In this region, river sediments are used in large quantities as building material. Therefore, the knowledge of the radionuclides distribution in such sediments is important for assessing their potential adverse effects on humans residing in buildings made of sediment material. For this goal, we focus on the determination of the natural radioactivity levels and magnetic properties in sediment samples collected from 33 locations along the southwestern Bharathapuzha river originating from the Anamalai hills. The sediment samples were subdivided into two categories according to particle size. It is observed that the average activity concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K in sediment samples varied greatly with granulometric and geological differences. The average values of ²²⁶Ra, ²³²Th, and ⁴⁰K and its associated radiological hazard parameters for category II samples (particle size between 149 μm and 2 mm) were lower than category I sediment samples (bulk samples). Moreover, the average radionuclide activity concentrations (except for ⁴⁰K) and the calculated radiation hazard parameters are higher in the lowland region compared to the highland and the midland regions. The mass-specific magnetic susceptibility values ranged widely along the river, as well as between physiographic regions, e.g., average values for category I sediment samples were 950.2 × 10^?8, 351.1 × 10^?8 and 131.8 × 10^?8 m³ kg^?1 (for high-, mid- and lowland regions, respectively). Differences between physiographic regions and sediment fractions from both radioactivity determinations and magnetic parameters were analyzed with statistical tests and multivariate analysis, which showed the advantages of using both independent techniques.     

Influence of friction on erosion and accretion processes in the Yavaros Bay,Gulf of California

A two-dimensional, vertically integrated, nonlinear numerical model was applied to investigate the tide-driven bed load transport of sediments and morphodynamics in the shallow coastal lagoon of Yavaros, located in the southeastern part of the Gulf of California, Mexico. Satellite imagery exposes strong sediment dynamics in this coastal region. The dynamics in the lagoon were forced by 13 tidal constituents at the open boundary. Tides are of a mixed character and they are predominantly semidiurnal. The calculations showed areas of intense tidal currents and considerable water exchange with the Gulf of California. Numerical experiments revealed an ebb-dominant tidal distortion and a net export of sediment from the lagoon to the Gulf of California. A simulation of 20 years showed that the lagoon exported about 1,600 m³ of sediment; however, the daily oscillating exchange of sediment reached values of around 8 m³. The daily averaged flux of export–import sediments oscillates principally with semiannual, monthly and fortnightly periods. By applying a threshold velocity, a variable friction coefficient and the calculated amplitude of tidal velocities, it was possible to determine that morphological changes occur in zones of sharp topographic gradients and to explain the effect of friction on the export–import process of sediments. A 10-year simulation revealed that accumulation of sediment (~20 cm) occurred in small areas, whereas erosion occurred in larger areas but with less intensity (~8 cm). Besides the importance for the morphodynamics, these kinds of erosion–accretion processes may be relevant for the marine ecology.     

Uranium geochemistry on the Amazon shelf: Evidence for uranium release from bottom sediments

In Amazon-shelf waters, as salinity increases to 36.5 × 10⁻³, dissolved uranium activities increase to a maximum of 4.60 dpm 1⁻¹. This value is much higher than the open-ocean value (2.50 dpm 1⁻¹), indicating a source of dissolved uranium to shelf waters in addition to that supplied from open-ocean and riverine waters. Uranium activities are much lower for surface sediments in the Amazon-shelf seabed (mean: 0.69 ±.09 dpm g⁻¹) than for suspended sediments in the Amazon River (1.82 dpm g⁻¹). Data suggest that the loss of particulate uranium from riverine sediments (and the consequent input of dissolved uranium to shelf waters) is probably the result of uranium desorption from the ferric-oxyhydroxide coatings on sediment particles, and/or uranium release by mobilization of the ferric oxyhydroxides. The total flux (i.e., riverine flux plus desorbed-remobilized particulate flux) of dissolved ²³⁸U from the Amazon shelf (about 1.2 × 10¹⁵ dpm yr⁻¹) constitutes about 15% of uranium input to the world ocean, commensurate to the Amazon River's contribution to world river-water discharge (approximately 18%). Measurement of only the riverine flux of dissolved ²³⁸U underestimates, by a factor of about 5, the flux of dissolved²³⁸U from the Amazon shelf to the open ocean.     

Trace metal and radionuclide pollution in marine sediments of the Aegean Sea (Izmir Bay and Didim)

To determine radioactivity and trace metal levels, surface sediments were collected from two important areas (?zmir Bay and Didim) in the Aegean Sea region of Turkey, and were analyzed for concentrations of ²¹⁰Po, ²¹⁰Pb and trace metals (Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn). The average ²¹⁰Po and ²¹⁰Pb massic activities in sediments varied in the range of 24 ± 5 to 126 ± 6 Bq kg^?1 dry wt. and 18 ± 3 to 59 ± 4 Bq kg^?1 dry wt., respectively. Izmir Bay exhibited the highest polonium activities in sediments, likely due to specific sedimentation processes and other sediment characteristics. The trace metal results showed that the Izmir Bay is facing trace metal pollution. The metal concentrations in sediment samples are low compared to those from the other neighboring marine environments.     

Land use,sediment loads and dispersal pathways from two catchments at the southern end of Lake Tanganyika,Africa: implications for lake management

Increasing sediment loads entering the Lake Tanganyika ecosystem are hastening the need for improved understanding of the linkages between catchment characteristics and influent sediment transport and loading. Sediment loads of two catchments at the southern end of the lake were estimated for October 1998–December 1999, and catchment characteristics determined using GIS. It was found that both sediment yields and loads were higher from the catchment of the Lunzua River (19.8 t km^?2 and 20,114 t, respectively) compared with that of the Kalambo (4.1 t km^?2 and 12,197 t) in 1999. These differences were both attributed to the smaller size and higher road density of the Lunzua catchment, and suggest that previous recommendations regarding the positioning of underwater lake reserves fail to take into account the low sediment retention capacity of small mountainous rivers. Differences between the study rivers in the transport of suspended sediments, organic matter, and bedload sediments into the lake were also found, the latter determined by the novel application of the 'McLaren Model'.     

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.     

The effect of distribution processes on the isomeric composition of hexachlorocyclohexane in a contaminated riverine system

Various factors influence the isomeric composition of hexachlorocyclohexanes which are released to the environment. Original compositions in technical mixtures may vary slightly, but higher shifts are observable for transfer processes, bioaccumulation and microbial transformation. Consequently, the isomeric composition in environmental samples is a superposition of these processes. In this study, isomeric distributions and concentrations of hexachlorocyclohexanes were analyzed in water, sediment, and soil samples of a riverine system known to be highly contaminated by hexachlorocyclohexanes. To assess desorption of hexachlorocyclohexanes from particulate matter to water, batch shaking and percolation experiments were conducted complementary. Analyzed samples exhibited total hexachlorocyclohexane concentrations of up to 2.8 µg/g in sediments and up to 21 µg/L in river water predominated by the α-isomer. Downstream hexachlorocyclohexane pattern changed toward δ-isomer domination, while overall hexachlorocyclohexane concentrations decreased. Desorption experiments supported the assumption of discrimination by preferred association of the α- and β-isomers with particulate matter, showing elevated mobilization of γ-, δ- and ε-hexachlorocyclohexanes and lower mobilization of the α- and β-isomers. Soil samples of a riparian wetland exhibited elevated concentrations of hexachlorocyclohexanes exceeding 200 µg/g and predominance of α-hexachlorocyclohexanes in the top soil layer. Subjacent soil layers showed rapidly decreasing hexachlorocyclohexane concentrations and an isomeric shift toward the β-isomer. The assumed preferential mobilization of β-hexachlorocyclohexane was supported by desorption experiments. This study demonstrated firstly that transfer processes influence substantially hexachlorocyclohexane isomer distribution in the aquatic environment. Secondly, conditions of aging determine strength of association and remobilization potential of hexachlorocyclohexane residue down to an isomer-specific level.     

Anaerobic Carbon Mineralisation Through Sulphate Reduction in the Inner Shelf Sediments of Eastern Arabian Sea

Monsoon-induced coastal upwelling, land run-off, benthic and atmospheric inputs make the western Indian shelf waters biologically productive that is expected to lead to high rates of mineralisation of organic matter (OM) in the sediments. Dissimilatory sulphate reduction (SR) is a major pathway of OM mineralisation in near-shore marine sediments owing to depletion of other energetically more profitable electron acceptors (O₂, NO₃ ^?, Mn and Fe oxides) within few millimetres of the sediment-water interface. We carried out first ever study to quantify SR rates in the inner shelf sediments off Goa (central west coast of India) using the ³⁵S radiotracer technique. The highest rates were recorded in the upper 10 cm of the sediment cores and decreased gradually thereafter below detection. Despite significant SR activity in the upper ～12 to 21 cm at most of the sites, pore water sulphate concentrations generally did not show much variation with depth. The depth integrated SR rate (0.066–0.46 mol m^?2 year^?1) decreased with increasing water depth. Free sulphide was present in low concentrations (0–3 μM) in pore waters at shallow stations (depth <30 m). However, high build-up of sulphide (100–600 μM) in pore waters was observed at two deeper stations (depths 39 and 48 m), 7–11 cm below the sediment-water interface. The total iron content of the sediment decreased from ～7 to 5 % from the shallowest to the deepest station. The high pyrite content indicates that the shelf sediments act as a sink for sulphide accounting for the low free sulphide levels in pore water. In the moderately organic rich (2–3.5 %) sediments off Goa, the measured SR rates are much lower than those reported from other upwelling areas, especially off Namibia and Peru. The amount of organic carbon remineralised via sulphate reduction was ～0.52 mol m^?2 year^?1. With an estimated average organic carbon accumulation rate of ～5.6 (±0.5) mol m^?2 year^?1, it appears that the bulk of organic matter gets preserved in sediments in the study region.     

Exploratory study on improving the benthic environment in sediment by sediment microbial fuel cells

Benthos cannot survive in strongly reduced sediments, in which the redox potential is around ?400 mV. Such sediments are typically found in inner harbors that are exposed to wastewater discharges. Field experiments were conducted to investigate the potential of sediment microbial fuel cells (SMFCs) for improving the benthic environment in such sediments. To the best of our knowledge, this has not been reported in any previous literature. Bottom sediment was collected and used to fuel an SMFC suspended 500 mm below the water surface. The sediments then were collected one year after installation, and their benthos environment was investigated. The most remarkable results are that the diversity and growth of benthos were higher in the SMFC-applied sediment than in a control sediment. The results have further strengthened that the sediment remediation was enhanced, in which the oxygen consumption rate of the sediment was reduced, and the mineralization of the organic matter was increased. Our findings suggest that SMFCs are a promising technology for the remediation of strongly reduced sediment and for the improvement of the benthic environment.     

Phosphorus Cycling and Burial in Sediments of a Seasonally Hypoxic Marine Basin

Recycling of phosphorus (P) from sediments contributes to the development of bottom-water hypoxia in many coastal systems. Here, we present results of a year-long assessment of P dynamics in sediments of a seasonally hypoxic coastal marine basin (Lake Grevelingen, the Netherlands) in 2012. Sequential phosphorus extractions (SEDEX) and X-ray absorption spectroscopy (XAS) indicate that P was adsorbed to Fe-(III)-(oxyhydr)oxides when cable bacteria were active in the surface sediments in spring. With the onset of summer hypoxia, sulphide-induced dissolution of the Fe-(III)-(oxyhydr)oxides led to P release to the pore water and overlying water. The similarity in authigenic Ca-P concentrations in the sediment and suspended matter suggest that Ca-P is not formed in situ. The P burial efficiency was ≤ 32%. Hypoxia-driven sedimentary P recycling had a major impact on the water-column chemistry in the basin in 2012. Water-column monitoring data indicate up to ninefold higher surface water concentrations of phosphate in the basin in the late 1970s and a stronger hypoxia-driven seasonal P release from the sediment. The amplified release of P from the sediment in the past is attributed to the presence of a larger pool of Fe-bound P in the basin prior to the first onset of hypoxia. Given that P is not limiting, primary production in the basin has not been affected by the decadal changes in P availability and recycling over the past 40 years. The changes in P dynamics on decadal time scales were not recorded in sediment profiles of total P or organic C/total P.     

The landscape-scale relationship between lake sediment geochemistry and catchment bedrock composition from the Temagami and Gowganda areas of Northeastern Ontario,Canada

Lake sediments are integrators of watershed wide environmental information that includes bedrock geology, glacial overburden, vegetation, hydrology and land use. Lake sediments were collected from an area covering approximately 13,600 km² from the Gowganda and Temagami regions to determine the geochemical background conditions representing different bedrock types. For the entire dataset, the median value for arsenic in lake sediment was 2.6 mg/kg, well within the prescribed limits indicating that the Canadian national objective for arsenic in sediments for the protection of aquatic life (17 mg/kg). Overall, the vast majority of lake sediment samples (97.2%) were below the 17 mg/kg Canadian objective for the protection of aquatic life, however, catchments with Nipissing Diabase had the highest background levels for arsenic (10 mg/kg) with some lakes ranging up to 30 mg/kg. The major geological controls influencing changes in lake sediment geochemistry were determined using random forest classification and principal component analysis (PCA). Random forest classification was able to identify which geological province the samples were derived from and the dominant rock types in the sample catchment with respectable accuracy. PCA revealed strong spatial relationships between lake sediment geochemistry and bedrock geology, particularly a strong relationship between Nipissing Diabase in the watershed of the lake and the cobalt-type mineralization indicator elements in the lake sediment including naturally higher levels of arsenic. Within the samples that exceeded regulatory standards, over half the samples that exceeded the regulatory objectives were located in watersheds that contained Nipissing Diabase in their catchment. This study demonstrates that unique geochemical assemblages can be associated with specific geological areas which is of interest to exploration geologists, for target generation and prospecting, and to environmental policy makers, for site-specific restoration targets.     

Mercury colonial footprint in Darién Gulf sediments,Colombia

The mercury (Hg) deposition history in the Darién Gulf is reconstructed from three sediment cores spanning up to 1,000 years. Knowledge on the contribution to global Hg budget from the Caribbean is limited. Patterns of water circulation, sediment deposition rates, cataclysmic atmospheric inputs, and post-depositional migration have been considered in Hg trapping in the seabed. The sediment delivery rates to the coastal zone over the Late Holocene have increased from 0.2 to 1 cm year^?1 owing to anthropogenic influence. This alteration took the form of geological effects, like coastal morphology change, that played a major role in Hg downcore signal preservation. Natural background Hg levels in Southern Caribbean sediments (77.0 μg kg^?1) are up to three times higher than preindustrial signals at other latitudes, because of volcanic contributions from the Pacific ring of fire. Enrichment factors rose from 0.9 to 1.5 (70.1–113.5 μg kg^?1) within profiles related to Hg usage since Spanish colonial times between the calendar years 1550 and 1811.     

Heavy metal accumulation in the surficial sediments along southwest coast of India

Concentration and distribution of heavy metals (Cd, Cr, Cu, Hg, Ni, Pb and Zn) in surface sediments collected from five stations located along the southwest coast of India were investigated seasonally to assess whether there is insidious buildup of heavy metals. Spatial variation was in accordance with textural characteristics and organic matter content. The concentration of the metals in sediments of the study area followed the order: Zn > Cr > Ni > Cu > Pb > Cd > Hg. The use of geochemical tools and sediment quality guidelines to account for the magnitude of heavy metal contamination revealed high contamination in monsoon and impoverishment during post-monsoon. Estimated total metal concentrations in the present investigation were comparable with other studies; however, concentrations of Ni and Zn were higher than that of other coastal regions. Concentrations of metals in sediment largely exceed NOAA effects range:low (e.g., Cu, Cr, Hg) or effects range:median (e.g., Ni) values. This means that adverse effects for benthic organisms are highly probable.     

The distribution, sources and toxicity risks of polycyclic aromatic hydrocarbons and n-alkanes in riverine and estuarine core sediments from the Daliao River watershed

The burial characteristics and toxicity risks associated with n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in the riverine and estuarine sediments of the Daliao River watershed were investigated based on three sediment cores. The sum of the n-alkane and PAH concentrations, normalized to organic carbon (OC), ranged from 0.27 to 63.09 μg g^?1OC^?1 and 6.60 to 366.20 μg g^?1OC^?1, respectively. The features and the history of industrial activities, such as the oil and chemical industries and port activities near the river and estuary, resulted in different distributions and sources of hydrocarbons. The sources of pollution were identified based on n-alkane indexes and on diagnostic ratios of PAHs. The diagnostic ratios indicated that the n-alkanes were derived from both biogenic and petrogenic sources in different proportions and that the PAHs were derived primarily from petrogenic combustion sources. A hierarchical cluster analysis grouped the core samples into two clusters. The first cluster, river sediments, corresponded to industrial activities; the second cluster, estuarine sediments, corresponded to port shipping activities. The toxic potency of the PAHs in the cores was assessed in terms of toxic equivalents (TEQs) of dibenzo[a,h]anthracene and benzo[a]pyrene. The top layer of the sediment in the cores had a relatively high toxicity. The TEQ values for benzo(a)pyrene (TEQ_BaP) and dioxins (TEQ_TCDD) furnished a consistent assessment of the PAHs in the sediment cores.     

A case study considering the comparability of mass and volumetric suspended sediment data

Contemporary real-time instruments that advance suspended sediment monitoring capabilities often provide results in units (e.g. volumetric) that are not easily comparable to traditional mass (e.g. gravimetric) methods. A Midwest case study was initiated to assess the accuracy of three methods commonly used to convert volumetric data to mass. Water samples from rural, suburban, and urban stream reaches were analyzed for suspended sediment concentration using laser diffraction and wet sieving methods, resulting in paired volumetric (μl/l) and mass (mg/l) suspended sediment concentrations. Observed volumetric data were converted to mass using an assumed particle density (Pd) of 2.65 g/cm³, a calculated Pd, and linear regression. Using the assumed Pd, estimated mass data differed from observed mass data by as much as 60 %. Dividing mass concentration (mg/l) by the volumetric concentration (μl/l) resulted in site-specific average suspended sediment particle densities ranging from 2.17, 1.99, 1.76 g/cm³ for different land use types. Using a calculated Pd, estimated mass data differed from observed mass data by as much as 45 %. Paired sample t tests showed observed and estimated mass values to be significantly different (p < 0.01). R ² values for regression equations ranged from 0.82 to 0.88. Conversion difficulties likely result from temporal and spatial variations of Pd. The results illustrate the imprecision of conversion methods and highlight possible estimation errors assuming idealized conditions. Continued work is necessary to improve quantitative relationship(s) between mass and volumetric suspended sediment data and the utility of both types of information for science and land management practices.     

Variability in upwelling intensity and nutrient regime in the coastal upwelling system offshore Namibia: results from sediment archives

The coastal upwelling system offshore Namibia is ideally suited to address a focal question of the Integrated Marine Biogeochemistry and Ecosystem Research Programme: what are the mechanisms that drive long-term changes in ecosystems? Considerable interannual variability in climatic forcing is indicated by long time series of meteorological and remote sensing observation; these accompany considerable interannual to interdecadal changes in the upwelling intensity over the last 100 years, as well as a centennial trend. On longer time scales, the only archives available are sediment records spanning the late Holocene. To decipher the sediment record, we mapped surface-sediment patterns of proxies for physical (sea surface temperature/SST from alkenone unsaturation indexes) and nutrient (δ¹⁵N on bulk sedimentary N) variables. Their present-day surface-sediment patterns outline the coastal upwelling cells and filaments and associated high productivity area. Analysed in an array of dated sediment cores, the spatial patterns of SST suggest long-term (>100 years) variability in the location and intensity of individual upwelling cells. The patterns of δ¹⁵N outline an area of intense denitrification near the coast, and advection of water with low-oxygen concentrations in the undercurrent from the North. δ¹⁵N exhibits considerable downcore variability, in particular over the last 50 years. The variability appears to be governed by differences in extent of denitrification and thus of the shelf oxygen balance, which appears to have deteriorated in the last 50 years. Together, the data suggest that SST and denitrification conditions have remained in the narrow bounds outlined by today’s patterns in surface sediments, but that spatially small variability in upwelling intensity and make-up of upwelling feed waters induced considerable changes in the lower trophic levels of the coastal upwelling ecosystem over the last 6,000 years. Attempts to correlate proxy records from sediments with observational time series and regional climate reconstructions were not successful, possibly because annual to interannual environmental signals are erased in the process of sediment formation.     

Distribution and source of organochlorine pesticides (OCPs) in the sediments of Poyang Lake

The concentrations of typical organochlorine pesticides (OCPs) (DDTs, HCHs, PCP-Na, and HCB) were measured to understand distribution and source of OCPs in surface and columnar sediments of Poyang Lake in 2006. And OCPS concentrations in surface sediment in 2017 were made a comparison with those in 2006 at several same sampling sites. OCPs showed higher concentrations in main stream than in river mouths (entrance of river flow into lake) of the lake. The average concentrations of HCHs and DDTs were 4.63 ± 3.86 and 20.15 ± 26.86 ng/g in surface sediments in 2006, respectively. Concentrations of OCPs in 2017 were lower than in 2006, such as HCHs average 1.98 ± 2.04 ng/g and DDTs average 4.87 ± 1.48 ng/g in 2017, indicating historical residual and degradation. The primary isomers of HCHs and DDTs in the lake were α-HCH, γ-HCH and p,p′-DDD, respectively. HCHs were from historical residual and lindane application. DDTs were from historical residual. PCP-Na total concentrations in surface sediment were 77.36 ng/g in 2006 and 44.04 ng/g in 2017. The concentration of HCB residues in surface sediment was 0.92 ± 0.90 ng/g in 2006 and 0.42 ± 0.38 ng/g in 2017. The concentrations of OCPs in columnar sediments showed annual variations, and the peak concentrations occurred in 1953, 1961, 1974, 1982, and 1995, showing close relations with onset of production OCPs pesticide in 1950s and its later prohibition in 1980s and a large number agricultural cultivated land decrease in 1990s in China. The concentrations of HCB in columnar sediments were average 2.33 ± 1.26 ng/g. OCPs of columnar sediments were from historical residues and lindane input. The main contamination of OCPs was PCP-Na and p,p′-DDD in Poyang Lake. On the whole, the combination of surface samples (0–5 cm in depth) and columnar samples (0–38 cm in depth) in a single study would give insight into OCPs pollution levels in different years (temporal resolution) and in different regions (spatial resolution) in Poyang Lake.