Dissolved humic substances supplied as potential enhancers of Cu, Cd, and Pb adsorption by two different mangrove sediments

Purpose The external supply of humic substances has been recently suggested for the remediation of metal-polluted sediments; however, little is known about how to supply them and their effects on metal mobility. The study sought to investigate the sediment\u2014metals\u2014humic substance interaction in mangrove forest sediments. We aimed to evaluate the sediment adsorption potential in the case of large and rapid metal loads, as recently occurred in the Doce River (Brazil). Materials and methods In each mangrove forest sampling point of the Benevente River (RB) and Vitoria bay (MO), sediments were collected randomly along the river banks at a depth of 0\u201310 cm. Samples were characterized in terms of pH, CEC, organic carbon, texture, specific surface area, and elemental composition. The heavy metal content was measured by mass absorption spectrophotometry. Humic substances were extracted from the sediments according to the International Humic Substances Society (IHSS) method, avoiding separation of fulvic and humic acids. Original sediments were supplemented with humic substances and six Cu, Cd, or Pb concentrations. Freundlich and Langmuir equations were employed to create adsorption isotherms. Results and discussion The two sediments are significantly different, specifically with regard to organic carbon and Fe content, texture, and specific surface area. External humic substances increased the Cu adsorption capacity in both sediments but without an important change in Cu adsorption dynamics. Humic substances slightly increased the sediment adsorption capacity of Pb in RB sediment while they decreased in MO sediment, characterized by lower specific surface area, probably due to coverage of the active adsorption sites. Cd isotherms showed that the different characteristics of sediments alone do not affect Cd adsorption, but coupled with humic substances; Cd affinity for the soil surface increased five times in RB sediments confirming sediment-metal- humic substance interactions. Conclusions Humic substances affect soil metal retention mainly by altering the ion affinity for sediment surface, leading to contrasting results. The Fe concentration could be important depending on specific surface area and humic substance percentage, due to its capacity to form spheroids linked to molecules of humic substances on the clay surface. Several works have been carried out on this research area, but due to the many variables and different metal ions, we recommend further studies

Characterization of specificity of bacterial community structure within the burrow environment of the marine polychaete Hediste (Nereis) diversicolor

Bioturbation is known to stimulate microbial communities, especially in macrofaunal burrows where the abundance and activities of bacteria are increased. Until now, these microbial communities have been poorly characterized and an important ecological question remains: do burrow walls harbor similar or specific communities compared with anoxic and surface sediments? The bacterial community structure of coastal sediments inhabited by the polychaete worm Hediste diversicolor was investigated. Surface, burrow wall and anoxic sediments were collected at the Carteau beach (Gulf of Fos, Mediterranean Sea). Bacterial diversity was determined by analyzing small subunit ribosomal RNA (16S rRNA) sequences from three clone libraries (168, 179 and 129 sequences for the surface, burrow wall and anoxic sediments, respectively). Libraries revealed 306 different operational taxonomic units (OTUs) belonging to at least 15 bacterial phyla. Bioinformatic analyses and comparisons between the three clone libraries showed that the burrow walls harbored a specific bacterial community structure which differed from the surface and anoxic environments. More similarities were nevertheless found with the surface assemblage. Inside the burrow walls, the bacterial community was characterized by high biodiversity, which probably results from the biogeochemical heterogeneity of the burrow system

Geochemistry of reduced inorganic sulfur, reactive iron, and organic carbon in fluvial and marine surface sediment in the Laizhou Bay region, China

Understanding the geochemical cycling of sulfur in sediments is important because it can have implications for both modern environments (e.g., deterioration of water quality) and interpretation of the ancient past (e.g., sediment C/S ratios can be used as indicators of palaeodepositional environment). This study investigates the geochemical characteristics of sulfur, iron, and organic carbon in fluvial and coastal surface sediments of the Laizhou Bay region, China. A total of 63 sediment samples were taken across the whole Laizhou Bay marine region and the 14 major tidal rivers draining into it. Acid volatile sulfur, chromium (II)-reducible sulfur and elemental sulfur, total organic carbon, and total nitrogen were present in higher concentrations in the fluvial sediment than in the marine sediment of Laizhou Bay. The composition of reduced inorganic sulfur in surface sediments was dominated by acid volatile sulfur and chromium (II)-reducible sulfur. In fluvial sediments, sulfate reduction and formation of reduced inorganic sulfur were controlled by TOC and reactive iron synchronously. High C/S ratios in the marine sediments indicate that the diagenetic processes in Laizhou Bay have been affected by rapid deposition of sediment from the Yellow River in recent decades

Spatial and temporal trends of iron and iron isotope cycling in the Peruvian oxygen minimum zone

Iron (Fe) is a key element in the global ocean’s biogeochemical framework because of its essential role in numerous biological processes. A poorly studied link in the oceanic Fe cycle is the reductive release of Fe from sediments in oxygen depleted ocean regions - the oxygen minimum zones (OMZs). Changing rates of Fe release from OMZ sediments may have the potential to modulate ocean fertility which has far-reaching implications considering the high amplitude oxygen fluctuations throughout earth history as well as the ongoing ocean deoxygenation projected for the near future. In order to explore spatial and temporal trends of Fe cycling in OMZs, we present here Fe isotope and speciation data for surface sediments from a transect across the Peruvian upwelling area, one of the most pronounced OMZs of the modern ocean. Because of continuous dissimilatory Fe reduction and diffusive loss across the benthic boundary, sediments within the OMZ are strongly depleted in reactive Fe components, and the little reactive Fe left behind has a heavy isotope composition. In contrast, surface sediments below the OMZ are enriched in reactive Fe, with the majority being present as Fe oxides with comparably light isotope composition. This lateral pattern of Fe depletion and enrichment indicates that Fe released from sediments within the OMZ is reoxidized and precipitated at the oxycline. First-order calculations suggest that the amount of Fe mobilized within the OMZ and that accumulated at the boundaries are largely balanced. Therefore, benthic Fe fluxes in OMZs should be carefully evaluated prior to incorporation into global models, as much of the initially released Fe may be reprecipitated prior to vertical or offshore transport. First XRF core scanning results for partly laminated piston cores from the OMZ boundaries reveal downcore oscillations in the content of reactive Fe and redox-sensitive trace metals that are attributed to past changes in OMZ extension. Ongoing work on these cores will focus on their dating and the downcore investigation of Fe and trace metal records in order to better understand past Fe cycling within the Peruvian OMZ and potential interactions with climate variability

Subsonic near-surface P-velocity and low S-velocity observations using propagator inversion

Detailed knowledge of near-surface P- and S-wave velocities is important for processing and interpreting multicomponent land seismic data because (1) the entire wavefield passes through and is influenced by the near-surface soil conditions, (2) both source repeatability and receiver coupling also depend on these conditions, and (3) near-surface P- and S-wave velocities are required for wavefield decomposition and demultiple methods. However, it is often difficult to measure these velocities with conventional techniques because sensitivity to shallow-wave velocities is low and because of the presence of sharp velocity contrasts or gradients close to the earth's free surface. We demonstrate that these near-surface P- and S-wave velocities can be obtained using a propagator inversion. This approach requires data recorded by at least one multicomponent geophone at the surface and an additional multicomponent geophone at depth. The propagator between them then contains all information on the medium parameters governing wave propagation between the geophones at the surface and at depth. Hence, inverting the propagator gives local estimates for these parameters. This technique has been applied to data acquired in Zeist, the Netherlands. The near-surface sediments at this site are unconsolidated sands with a thin vegetation soil on top, and the sediments considered are located above the groundwater table. A buried geophone was positioned 1.05 m beneath receivers on the surface. Propagator inversion yielded low near-surface velocities, namely, 270 ± 15 m/s for the compressional-wave velocity, which is well below the sound velocity in air, and 150 ± 9 m/s for the shear velocity. Existing methods designed for imaging deeper structures cannot resolve these shallow material properties. Furthermore, velocities usually increase rapidly with depth close to the earth's surface because of increasing confining pressure. We suspect that for this reason, subsonic near-surface P-wave velocities are not commonly observed

Influence of sediment redox conditions on uranium mobilisation during saline intrusion

This research was funded by the Natural Environment Research Council (grant NE/C506799/1: Studentship NE/H527116/1).In the UK, several coastal nuclear sites have been identified as vulnerable to future sea level rise. Legacy contamination at these sites has accumulated in sub-surface sediments at risk of future seawater inundation and intrusion. Porewater salinization, changes in pH and the influx of oxygen into sediments may impact the stability of sediment associated uranium (U). In this study, saturated column experiments were performed to compare the mobilisation of U from oxic and reduced sediments into seawater under environmentally relevant flow conditions. Uranium release profiles were independent of the initial geochemistry of the sediments. Uranium release from the sediments was kinetically controlled, showing relatively slow desorption kinetics, with release initially limited by the impact of the sediments on the pH of the seawater. Significant U release only occurred when the pH was sufficiently high for the formation of U-carbonate complexes (pHoxic 6.3; pHreduced 7.5). Uranium was more strongly bound to the reduced sediments and after 400 pore volumes of seawater flow, release was more extensive from the initially oxic (46%) compared with initially nitrate reducing (27%) and iron reducing (18%) sediments. The products of iron cycling appeared to act as a buffer limiting U mobilisation, but the on-going dissolution of the Fe-phases suggests that they did not form a permanent protective layer. © 2013 Elsevier B.V

Use of rare earth oxides as tracers to identify sediment source areas for agricultural hillslopes

Understanding sediment sources is essential to enable more effective targeting of in-field mitigation approaches to reduce diffuse pollution from agricultural land. In this paper we report on the application of rare earth element oxides to arable soils at hillslope scale in order to determine sediment source areas and their relative importance, using a non-intrusive method of surface spraying. Runoff, sediments and rare earth elements lost from four arable hillslope lengths at a site in the UK with clay soils were monitored from three rainfall events after tracer application. Measured erosion rates were low, reflecting the typical event conditions occurring at the site, and less than 1% of the applied REO tracers were recovered, which is consistent with the results of comparable studies. Tracer recovery at the base of the hillslope was able to indicate the relative importance of different hillslope sediment source areas, which were found to be consistent between events. The principal source of eroded sediments was the upslope area, implying that the wheel tracks were principally conduits for sediment transport, and not highly active sites of erosion. Mitigation treatments for sediment losses from arable hillslopes should therefore focus on methodologies for trapping mobile sediments within wheel track areas through increasing surface roughness or reducing the connectivity of sediment transport processes

The Mersey Estuary : sediment geochemistry

This report describes a study of the geochemistry of the Mersey estuary carried out between April 2000 and December 2002. The study was the first in a new programme of surveys of the geochemistry of major British estuaries aimed at enhancing our knowledge and understanding of the distribution of contaminants in estuarine sediments. The report first summarises the physical setting, historical development, geology, hydrography and bathymetry of the Mersey estuary and its catchment. Details of the sampling and analytical programmes are then given followed by a discussion of the sedimentology and geochemistry. The chemistry of the water column and suspended particulate matter have not been studied, the chief concern being with the geochemistry of the surface and near-surface sediments of the Mersey estuary and an examination of their likely sources and present state of contamination

Abundance and Distribution of Enteric Bacteria and Viruses in Coastal and Estuarine Sediments—a Review

The long term survival of fecal indicator organisms (FIOs) and human pathogenic microorganisms in sediments is important from a water quality, human health and ecological perspective. Typically, both bacteria and viruses strongly associate with particulate matter present in freshwater, estuarine and marine environments. This association tends to be stronger in finer textured sediments and is strongly influenced by the type and quantity of clay minerals and organic matter present. Binding to particle surfaces promotes the persistence of bacteria in the environment by offering physical and chemical protection from biotic and abiotic stresses. How bacterial and viral viability and pathogenicity is influenced by surface attachment requires further study. Typically, long-term association with surfaces including sediments induces bacteria to enter a viable-but-non-culturable (VBNC) state. Inherent methodological challenges of quantifying VBNC bacteria may lead to the frequent under-reporting of their abundance in sediments. The implications of this in a quantitative risk assessment context remain unclear. Similarly, sediments can harbor significant amounts of enteric viruses, however, the factors regulating their persistence remains poorly understood. Quantification of viruses in sediment remains problematic due to our poor ability to recover intact viral particles from sediment surfaces (typically <10%), our inability to distinguish between infective and damaged (non-infective) viral particles, aggregation of viral particles, and inhibition during qPCR. This suggests that the true viral titre in sediments may be being vastly underestimated. In turn, this is limiting our ability to understand the fate and transport of viruses in sediments. Model systems (e.g., human cell culture) are also lacking for some key viruses, preventing our ability to evaluate the infectivity of viruses recovered from sediments (e.g., norovirus). The release of particle-bound bacteria and viruses into the water column during sediment resuspension also represents a risk to water quality. In conclusion, our poor process level understanding of viral/bacterial-sediment interactions combined with methodological challenges is limiting the accurate source apportionment and quantitative microbial risk assessment for pathogenic organisms associated with sediments in aquatic environments

Short-term fate of phytodetritus in sediments across the arabian sea oxygen minimum zone

The short-term fate of phytodetritus was investigated across the Pakistan margin of the Arabian Sea at water depths ranging from 140 to 1850 m, encompassing the oxygen minimum zone (~100–1100 m). Phytodetritus sedimentation events were simulated by adding ~44 mmol 13C-labelled algal material per m2 to surface sediments in retrieved cores. Cores were incubated in the dark, at in situ temperature and oxygen concentrations. Overlying waters were sampled periodically, and cores were recovered and sampled (for organisms and sediments) after durations of two and five days. The labelled carbon was subsequently traced into bacterial lipids, foraminiferan and macrofaunal biomass, and dissolved organic and inorganic pools. The majority of the label (20 to 100%) was in most cases left unprocessed in the sediment at the surface. The largest pool of processed carbon was found to be respiration (0 to 25% of added carbon), recovered as dissolved inorganic carbon. Both temperature and oxygen were found to influence the rate of respiration. Macrofaunal influence was most pronounced at the lower part of the oxygen minimum zone where it contributed 11% to the processing of phytodetritus