Sediment fluxes and the littoral drift along northeast Andhra Pradesh Coast, India: estimation by remote sensing

The littoral drift regime along the northeastern coast of India was investigated by analyzing coastal drift indicators and shoreline changes based on multitemporal satellite images. The study of offshore turbidity patterns and quantitative estimation of suspended sediments was undertaken to understand the magnitude and direction of movement of sediment fluxes. The study revealed that: (1) the character of coastal landforms and sedimentation processes indicate that the sediment transport is bidirectional and monsoon dependent; (2) multidate, multitemporal analysis of satellite images helps to show the nature of sediment transport along the coast. The dominant net sediment transport is in a NE direction along the eastern coast of India. Finally, this assessment demonstrates the potential of remote sensing technology in understanding the coastal morphometric changes, long-term sediment transport, shoreline changes, and offshore turbidity distribution pattern and the implications for the transport of sediment-associated pollutants.     

Shoreline change and potential sea level rise impacts in a climate hazardous location in southeast coast of India

Climate change impact on the environment makes the coastal areas vulnerable and demands the evaluation of such susceptibility. Historical changes in the shoreline positions and inundation based on projected sea-level scenarios of 0.5 and 1 m were assessed for Nagapattinam District, a low-lying coastal area in the southeast coast of India, using high-resolution Shuttle Radar Topography Mission data; multi-dated Landsat satellite images of 1978, 1991, 2003, and 2015; and census data of 2011. Image processing, geographical information system, and digital shoreline analysis system methods were used in the study. The shoreline variation indicated that erosion rate varied at different time scales. The end point rate indicated the highest mean erosion of ??3.12 m/year, occurred in 73% of coast between 1978 and 1991. Weighted linear regression analysis revealed that the coast length of 83% was under erosion at a mean rate of ??2.11 m/year from 1978 to 2015. Sea level rise (SLR) impact indicated that the coastal area of about 14,122 ha from 225 villages and 31,318 ha from 272 villages would be permanently inundated for the SLR of 0.5 and 1 m, respectively, which includes agriculture, mangroves, wetlands, aquaculture, and forest lands. The loss of coastal wetlands and its associated productivity will severely threaten more than half the coastal population. Adaptation measures in people participatory mode, integrated into coastal zone management with a focus on sub-regional coastal activities, are needed to respond to the consequences of climate change.     

Phosphorus speciation in the marine sediment of Kalpakkam coast,southeast coast of India

A study was carried out at Kalpakkam coast to find out the distribution of various fractions of phosphorus (P) in the marine sediment during pre-northeast monsoon period. Samples were collected from ten locations covering ~80 km² of the inner-shelf region. Sedimentary parameters such as sand, silt, clay, and organic carbon percentage were analyzed in order to find out their relation with various P fractions. The sediment was found to be predominantly sandy in nature with low silt and clay content. Among all the fractions (loosely bound (LoP), calcium bound (CaP), iron bound (FeP), aluminum bound (AlP), and organic (OP)), CaP fraction constituted the largest portion (68.7 %) followed by organic fraction (16.3 %). The bioavailable P fractions ranged from 5 to 44 % of the total P (TP) content. Relatively high LoP content was observed at the offshore locations with comparatively high mud percentage as compared with the near-shore locations. As FeP and AlP concentrations were directly proportional to the amount of fine-grain sediment, the low levels of these fractions found in this coastal area were therefore attributed to the sandy nature of the sediments. The order of abundance of the major forms of P in the surface sediments of Kalpakkam coast was as follows: CaP?>?OP?>?LoP?>?AlP?>?FeP.     

Geochemical characterisation of major and trace elements in the coastal sediments of India

Thirty-five surface sediment samples from the Indian continental shelf were recovered offshore from the mouths of the major rivers (Brahmaputra, Ganges, Narmada, Tapti, Godavari, Krishna and Cauvery) discharging into the coastal region of both east and west coasts were analysed using inductively coupled plasma atomic emission spectroscopy for selected major (i.e. Al, Ca, Fe, K, Ti, Mg and Na) and trace elements (e.g. Ba, Co, Cr, Cu, Ga, Ni, P and V), after total dissolution. The main objectives are to understand the processes controlling major and trace elements in the surface sediments and to identify natural and anthropogenic sources in the coastal environment using statistically regressed elemental concentrations to establish regional baseline levels. Metal enrichments observed close to the major urban areas in the east and west coasts are associated with the industrialised activities areas rich in Cu and Co in both the east and west coast sediments. Normalisation of metals to Al indicated that high enrichment factors are in the order of Ca>Ti≥Fe>Na>Mg>Co>Cu>Ga>V>Ba except K and P depletion. This indicated that the characteristic of estuarine sediment showed higher level along the west coast of India, which was reflected in the coastal sediments as similar to the source of its origin from the riverine composition and its abundances.     

Aliphatic and polycyclic aromatic hydrocarbons in the surface sediments of the Mediterranean: assessment and source recognition of petroleum hydrocarbons

Coastal marine sediment samples were collected from ten sampling stations along the Egyptian Mediterranean coast in April 2010. All sediment samples were analyzed for aliphatic (C7 to C34) and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC) contents and grain size analysis. Total aliphatic hydrocarbons ranged from 1621.82 to 9069.99 ng/g (dry weight), while aromatic hydrocarbons (16 PAHs) varied between 208.69 and 1020.02 ng/g with an average of 530.68?±?225.86 ng/g?dwt. Good correlations observed between certain PAH concentrations allowed to identify its origin. The average TOC percent was varied from 0.13 to 1.46 %. Principal component analysis was used to determine the sources of hydrocarbon pollutants in sediments of Mediterranean. Additionally, special PAHs compound ratios suggest the petrogenic origins.     

Levels, distribution, and risk assessment of organochlorines in surficial sediments of the Red Sea coast, Egypt

The analyses of environmentally persistent pollutants like polychlorinated biphenyls (PCBs), hexachlorocyclohexane (HCH) isomers, and dichlorodiphenyltrichloroethane (DDT) and its metabolites in surficial sediment samples collected from 17 locations along with the coast of the Red Sea in Egypt were carried out using gas chromatography–mass spectrometry. Several potential organic contaminants from agricultural (e.g., DDT and its breakdown products, lindane, endrin, dieldrin, and endosulfan) and industrial (PCBs) sources were measured. The levels of 20 organochlorine pesticides (OCPs) and ten PCB congeners in sediment collected from 17 stations along ~1,200 km were investigated. Concentrations of PCBs, HCHs, DDTs, and cyclodienes ranged from 0.40 to 6.17, 0.01 to 0.09, n.d. to 0.46, and 0.08 to 0.90 ppb dry weight. Two statistical programs were applied on the data (principal component analysis, PCA, and cluster analysis, CA), and it was concluded that it is impossible to predict the distribution patterns of the OCPs in a contaminated area. Risk assessment of the organochlorines contaminated in the sediments of the studied area was investigated.     

Organochlorine pesticide residues in sediments from coastal environment of Cantabria (northern Spain) and evaluation of the Atlantic Ocean

This paper documents levels of organochlorine pesticides (OCs) in coastal surface sediments from selected reference sites on the northern Atlantic Spanish coast. One hundred eight samples covering three estuaries in the Cantabrian Coast were sampled in 2006 and analyzed in the finer fraction (<63 ??m) for 19 OCs by gas chromatography with electron capture detector after confirmation by mass spectrometry. Detected organochlorine pesticides were endosulfan ??, endosulfan ??, endosulfan sulfate, hexachlorobenzene (HCB), aldrin, dieldrin, methoxychlor, 1,1-dichloro-2,2-bis(4-chlorophenyl)ethylene (4,4??-DDE) and 1,1-dichloro-2,2-bis(4-chlorophenyl)ethane (4,4??-DDD). Total OCs concentrations ranged from 1.8 ng g^???1 dry weight (dw) to 3.9 ng g^???1 dw, showing a uniform distribution along the studied area, and being consistent with recorded levels in the literature for coastal sediments in other reference sites with low levels of pollution by OCs along the Atlantic Ocean. Endosulfan, 4,4??-DDD, HCB, aldrin, and dieldrin seemed to be ubiquitous as the legacy of past uses and deposition. OCs concentrations were significantly correlated to organic matter content and particle size distribution. No adverse biological effects derived from these pollutants are expected to take place as it can be concluded from the comparison with the existent marine sediment quality guidelines.     

Spatial variation of potentially toxic elements in different grain size fractions of marine sediments from Gulf of Mannar, India

Marine sediments of the Gulf of Mannar (GoM), India are contaminated by potential toxic elements (PTEs) due to anthropogenic activities posing a risk to the existing fragile coral ecosystem and human health. The current study aimed to assess the distribution of PTEs (arsenic—As; cobalt—Co; copper—Cu, molybdenum—Mo; lead—Pb; and zinc—Zn) in marine sediments of different grain size fractions, viz., medium sand (710 μm), fine sand (250 μm), and clay (<63 μm) among the different coastal regions of Pamban, Palk Bay, and Rameswaram coasts of GoM, using grain size as one of the key factor controlling their concentrations. The concentrations of PTEs were measured in the different size fractions of sediment using inductively coupled plasma mass spectrophotometer. The order of accumulation of all PTEs in the three fractions was ranked as Zn > Cu > Pb > As > Co > Mo and in the three locations as Rameswaram > Palk Bay > Pamban. The concentration of PTEs in Palk Bay and Rameswaram coast was significantly different (P?<?0.05), when compared to Pamban coast. Measured geoaccumulation index (I _geo) and contamination factor (CF) indicated significant enrichment of Co and Pb from Rameswaram coast when compared to other two coasts. Although the concentration of Co was low but the measured I _geo and CF values indicated significant enrichment of this PTE in Rameswaram coast. The increased input of PTEs in the coastal regions of GoM signifies the need to monitor the coast regularly using suitable monitoring tools such as sediments to prevent further damage to the marine ecosystem.     

Sedimentation and remobilization of radiocesium in the coastal area of Ibaraki, 70 km south of the Fukushima Dai-ichi Nuclear Power Plant

Sedimentation and remobilization processes of radiocesium were investigated from time-series observations at nine stations in the coastal area of Ibaraki, 70–110 km south of the Fukushima Dai-ichi Nuclear Power Plant (1FNPP). Sediment samples were collected four times between June 2011 and January 2012, and concentrations of radiocesium as well as sediment properties such as grain size and elemental compositions were analyzed. Cumulative inventory of ¹³⁷Cs in sediment (0–10 cm) ranged between 4?×?10³ and 3?×?10⁴ Bq/m² as of January 2012. This amount was generally higher at stations nearer 1FNPP and has remained at the same level since August 2011. From these results, it can be inferred that dissolved radiocesium advected southward from the region adjacent to the 1FNPP and was deposited to the sediment of the study area in the early stage after the accident. The incorporation of radiocesium into sediments was almost irreversible, and higher concentrations of ¹³⁷Cs were obtained from the finer-grained fraction of sediments. In the northern offshore stations, resuspension of the fine-grained sediments formed a high-turbidity layer 10–20 m above the seabed. These results indicate that radiocesium-enriched fine particles were transported from the coast to offshore regions through the bottom high-turbidity layer.     

Heavy metal inputs evolution to an urban hypertrophic coastal lagoon, Rodrigo De Freitas Lagoon, Rio De Janeiro, Brazil

This work discusses the temporal variation of metal concentrations in a hypertrophic coastal lagoon located in the metropolitan area of Rio de Janeiro (Brazil). The lagoon watershed includes one of the mostly densely urbanized areas of the city but without industrial activities. Six sediment cores were collected in the lagoon between May and July 2003 and analyzed for the concentration of metals (Fe, Al, Mn, Zn, Pb, Cu, Cr, and Ni). Typical sedimentation rate was calculated as being 0.75 cm year^???1 and was uniform for at least the past 70 years. Therefore, the alterations in the dynamics of the lagoon caused by changes in its watershed were clearly indicated in sediment cores. The construction of an artificial canal to the sea and the increasing urbanization and soil use changes were the major factors affecting metal accumulation in the lagoon sediments. Metals typical of anthropogenic urban sources (Pb, Zn, and Cu) showed increasing loads following urbanization.     

Assessment of priority phenolic compounds in sediments from an extremely polluted coastal wetland (Lake Maryut, Egypt)

Although high concentrations of trace organic pollutants were recorded along the Egyptian Mediterranean Coast and its corresponding coastal wetlands, no published data are available for the levels of phenolic compounds. Thus, this work aimed to investigate the levels of phenolic compounds in sediments of a heavily polluted coastal wetland (Lake Maryut, Egypt). For that purpose, a method was optimized for the extraction and detection of chlorophenols, methylphenols, and nitrophenols in sediments using GC-MS. Sediments were extracted with 0.1 M NaOH/methanol by sonication. Cleanup of sediment extracts using liquid–liquid extraction and SPE was found important to remove most of the interfering co-extracts. The proposed analytical methodology was validated by analysis of matrix spikes. Detection limits were 0.063–0.694 μg/kg dw for sediments. Good recoveries (70–110%) and precision values (RSD?<?20%) were obtained from the fortification experiments at the parts per billion level in sediments. The method was applied to investigate the level of contamination with phenols in 19 sediment samples from Lake Maryut. Results revealed that higher concentrations were observed in the main basin (MB) of Lake Maryut affected by the discharge of effluents from a primary wastewater treatment plant, direct discharge of industrial effluents, domestic wastes, and agricultural effluents from Qalaa Drain (QD). Chlorophenols (CPs) were the major group detected in the lake sediments followed by methylphenols (MPs) and nitrophenols (NPs). CPs were dominated by 2-, 4-, and 3-chlorophenols. Concentrations of CPs were higher at the north and northwestern parts of the MB indicating the influence of industrial effluents discharged into the lake. On the other hand, higher concentrations of NPs were observed at the south and southwestern parts of the MB, which is subjected to the discharge of agricultural and domestic effluents via QD. Results of the risk assessment revealed that phenol, cresols, 2,4-dinitrophenol, 4-NP, 2-CP, 2,3,4,6-tetrachlorophenol and 2,4-dimethylphenol are contaminants of concern and that adverse ecological effects could possibly occur to benthic species from the exposure to these pollutants in Lake Maryut and thus phenols should be included in monitoring and pollution prevention programs in the Egyptian aquatic environment affected by anthropogenic activities.     

Enhanced anthropogenic heavy metal dispersal from tidal disturbance in the Jiaozhou Bay, North China

Heavy metal contamination in surface sediments of the Jiaozhou Bay was investigated in this study. Sediment sample was collected from the Jiaozhou Bay and its rivers. Heavy metal concentration was determined by inductively coupled plasma atomic emission spectroscopy and graphite furnace atomic absorption spectrometry. The result shows that river sediment in the east coast of the Jiaozhou Bay was heavily polluted especially for the Cu, Pb, Cd, and Zn. A slightly increase of heavy metal concentration was observed at stations near the east coast in the Jiaozhou Bay; however, contaminated sediment from polluted river was constrained mostly near shore within 3–4 km. Downstream decrease of heavy metals in river mouth suggested dilution from strong tidal current. Rapid seaward decline in the east coast and alongshore band dispersal pattern of heavy metals in surface sediment indicated mixing and remobilizing enhanced by large tidal range that regulated dispersal of sediments and anthropogenic heavy metals in the Jiaozhou Bay area.     

Phosphorous speciation in surface sediments of the Cochin estuary

Sequential chemical extraction using chelating agents were used to study the P dynamics and its bioavailability along the surface sediments of the Cochin estuary (southwest coast of India). Sediments were analyzed for major P species (iron bound P, calcium bound P, acid soluble organic P, alkali soluble organic P and residual organic P), Fe, Ca, total carbon, organic carbon, total nitrogen and total sulfur contents. An abrupt increase in the concentration of dissolved inorganic P with increasing salinity was observed in the study region. Iron-bound P exhibited a distinct seasonal pattern with maximum values in the monsoon season when fresh water condition was prevailed in the estuary. As salinity increased, the percentage of iron-bound P decreased, while that of calcium-bound P and total sedimentary sulfur increased. C/P and N/P ratios were low which indicate that large amounts of organic matter enriched with P tend to accumulate in surface sediments. The high organic P contribution in the sedimentary P pool may indicate high organic matter load with incomplete mineralization, as well as comparatively greater percentage of humic substance and resistant organic compounds. Principal component analysis is employed to find the possible processes influencing the speciation of P in the study region and indicate the following processes: (1) the spatial and seasonal variations of calcium bound P and acid soluble organic P was mainly controlled by sediment texture and organic carbon content, (2) sediment redox conditions control the distribution of iron bound P and (3) the terrigenous input of organic P is a significant processes controlling total P content in surface sediments. The bioavailable P was very high in the surface sediments which on an average accounts for 59 % in the pre-monsoon, 65 % in the monsoon and 53 % in the post-monsoon seasons. The surface sediments act as a potential internal source of P in the Cochin estuary.     

Impact of anthropogenic input on physicochemical parameters and trace metals in marine surface sediments of Bay of Bengal off Chennai, India

The study of heavy metal distribution in coastal surface sediments is an important component in understanding the exogenic cycling as well as in assessing the effect of anthropogenic influences on the marine ecosystem. In this study, surface sediment samples were collected from five different traverses along the innershelf of Bay of Bengal, off Chennai, India during pre- and post-monsoon seasons. The results of Spearmen correlation matrix, factor and cluster analysis, enrichment and contamination factor analysis, and geoaccumulation index of the heavy metals analyzed in the collected surface sediment were discussed. The level of both enrichment and contamination factor are shown in following order Cd > Cu > Cr > Ni > Pb > Co > Zn > Mn > Fe > Hg. The geoaccumulation index suggests that Cd and Cu are strongly to extremely pollute the sediments in both seasons. The results strongly indict anthropogenic sources for moderate input of Cd and Cu in to the innershelf of Chennai coast.     

Trace metals: Inputs, sedimentation and accumulation in San Vicente Bay, Chile

The present study deals with sediment dynamics affecting sediment-associated metal distributions in an embayment system experiencing pollution from coastal industries. Sedimentary metal content may originate from diagenetic processes of foundation rock on the bottom, allochthonous minerals from natural sources, and metals from industrial effluents along the coast. The study presents experimental estimations of quantities of metals entering the bay in industrial wastewater, measurements of metal content in particulate material captured in sediment traps, and metals distribution in surface sediments. Quantitative estimations of metals entering the system in industrial effluent showed the relation Pb Zn > Cu > Cr Ni > Cd. That of metals associated with particulate material from traps was Zn > Cr Cu > Pb > Ni > Cd and the abundance of metals in sediments was Zn > Cr > Cu > Pb > Ni > Cd. Finally, rates of bottom sediment accumulation are estimated in relation to the time of residence of water in the bay. The experimental data on sedimentation and sediment abundance were consistent with field observations on distribution and accumulation at sites of major sedimentation in this bay.     

Comparison of different methods for extraction of polycyclic aromatic hydrocarbons (PAHs) from Sicilian (Italy) coastal area sediments

This paper describes a work aimed at improving the conditions of an extraction method, coupling GC-MS determination, for the analysis without cleanup phase, of polycyclic aromatic hydrocarbons (PAHs) from sediment samples. The automatic Soxhlet extraction in warm mode (using Extraction System B-811 Standard, Büchi) has demonstrated advantages for automation, reduced extraction time, and lower solvent use than for conventional Soxhlet extraction. Under these conditions, the recoveries are very good as they resulted greater than 85 % and, in most of the cases, near 100 %. The repeatability is also satisfactory (relative standard deviation less than 15 %). The detection limits are also acceptable and ranged from 0.001 to0.01 μg/kg dry weight. Fifty-four sediment samples were collected. The total concentration of the 17 compounds investigated, in samples of sediments collected from three Sicilian coastal areas, expressed as the sum of concentrations, varies from 99 to 11,557 μg/kg of dry matrix; concentrations of total PAHs in the sediments of Cala are two to three times higher than the other stations.     

Spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in sediments of the Nansi Lake, China

Polycyclic aromatic hydrocarbons (PAHs) were measured in surface sediments and dated core sediments from the Nansi Lake of China to investigate the spatial and temporal distribution characteristics. The concentrations of 16 kinds priority PAH compounds were determined by GC-MS method. And ²¹⁰Pb isotope dating method was used to determine the chronological age of the sediment as well as the deposition rate. The results indicated that the total PAHs concentration ranges in surface and core sediment samples were 160 ~32,600 and 137 ~ 693 ng/g (dry wt.), respectively. The sediment rate and the average mass sedimentation were calculated to be 0.330 cm·year^???1 and 0.237 g·cm^???2·yr^???1 and the sediment time of the collected core sample ranged from 1899 to 2000. The peak of PAH concentrations came at recent years. The source analysis showed PAHs mainly came from the contamination of low temperature pyrogenic processes, such as coal combustion. The PAHs concentrations were lower than ERL and LEL values for most collected samples. However, in several surface sediment samples especially in estuary sites, the PAHs concentrations were not only higher than ERL and LEL values, but also higher than ERM values.     

Heavy metal concentrations in the surface marine sediments of Sfax Coast, Tunisia

Sixty-seven surface marine sediment samples in the <63 ?? m fraction collected from the coast of Sfax (Tunisia) were analyzed by inductively coupled plasma-atomic emission spectrometry for seven heavy metals (Pb, Ni, Cu, Cr, Zn, Cd, and Fe). Metal concentrations were compared with natural values, marine sediment quality standards, and also with other results concerning sediments from several Mediterranean coasts. The study of their spatial distributions refined by complementary approaches including principal component analysis, enrichment factors, and geoaccumulation index showed a significant impact of multiple anthropogenic sources. These included industrial sources and municipal discharges of the urban Sfax and also non-controlled discharges in rural zones close to the coastline. Moderate pollution of sediments, especially by Pb, Zn, and Ni, was shown to exist in localized sites. Besides, it was shown that other sites, slightly to highly enriched in terms of Cu, Cr, and Cd, are characterized by a quality of sediments varying from unpolluted to moderately polluted.     

Multi-year monitoring of estuarine sediments as ultimate sink for DDT, HCH, and other organochlorinated pesticides in Argentina

Forty-nine superficial sediment samples used in this study were collected from eight sites in the Bahia Blanca Estuary, located in the Buenos Aires Province southwest, Argentina, in a period between April 2005 and March 2009, to assess the concentration levels, spatial and seasonal distribution, and putative input sources of 18 selected organochlorine pesticides (OCs), following UNEP-IAEA procedures. Average concentration levels in sediments ranged between 3.54 and 63.79 ng g^???1, d.w. (mean = 15.99 ng g^???1, d.w.), for ??OCs, and from nondetectable to 8.03 ng g^???1, d.w. (mean = 2.16 ng g^???1, d.w.), and from nondetectable to 3.20 ng g^???1 (mean = 0.97 ng g^???1, d.w.) for hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs), respectively. Principal component analysis allowed the classification of sampling sites according to the main OCs inputs over the estuary. In comparison to other worldwide locations and to the world coastal sediment concentrations range, sediment DDTs and HCHs levels were in the low range; on the opposite, ??OCs average was in the medium range. OCs seasonal distribution was found to be highly correlated with the precipitations seasonality and sowing seasons in the adjacent agriculture fields. In addition, an ecotoxicological risk assessment pointed industrial and agriculture catchment zones with intermediate probability of adverse effects to biota, while the city sewage outfall was classified with none indication of an immediate threat. Data indicated that the estuary sediments were functioning as a sink for persistent OC pesticides (either in use or banned), however, it was found a declining trend on their environmental burden.     

Environmetrics to evaluate marine environment quality

The environmetric data analysis of analytical datasets from sediment and benthic organisms samples collected from different sampling sites along the coast of Black Sea near to City of Varna, Bulgaria has given some important indications about the bioindication properties of both type of samples. Various multivariate statistical methods like cluster analysis, principal components analysis, source apportioning modeling and partial least square (PLS) modeling were used in order to classify and interpret the parameters describing the chemical content of the coastal sediments (major components, heavy metals and total organic carbon) and benthic organisms (heavy metals). It has been shown that seriously polluted coastal zones are indicated in the same way by all benthic species, although some specificity could be detected for moderate polluted regions' e.g. polychaeta accumulated preferably Co, Cr, Cu, and Pb; crustacea - As, Cd, and Ni; mollusca - Zn. The identified latent factors responsible for the dataset structure are clearly indicated and apportioned with respect to their contribution to the total mass or total concentration of the species in the samples. The linear regression and PLS models indicated that a reliable forecast about the relation between naturally occurring chemical components and polluting species accumulated in the benthic organisms is possible.