Metal concentrations in sediments from tourist beaches of Miri City,Sarawak, Malaysia (Borneo Island)

Forty-three sediment samples were collected from the beaches of Miri City, Sarawak, Malaysia to identify the enrichment of partially leached trace metals (PLTMs) from six different tourist beaches. The samples were analyzed for PLTMs Fe, Mn, Cr, Co, Cu, Ni, Pb, Sr and Zn. The concentration pattern suggest that the southern side of the study area is enriched with Fe (1821–6097 μg g⁻¹), Mn (11.57–90.22 μg g⁻¹), Cr (51.50–311 μg g⁻¹), Ni (18–51 μg g⁻¹), Pb (8.81–84.05 μg g⁻¹), Sr (25.95–140.49 μg g⁻¹) and Zn (12.46–35.04 μg g⁻¹). Compared to the eco-toxicological values, Cr > Effects range low (ERL), Lowest effect level (LEL), Severe effect level (SEL); Cu > Unpolluted sediments, ERL, LEL; Pb > Unpolluted sediments and Ni > ERL and LEL. Comparative results with other regions indicate that Co, Cr, Cu, Ni and Zn are higher, indicating an external input rather than natural process.     

Source and distribution of lead in the surface sediments from the South China Sea as derived from Pb isotopes

Rapid economic development in East Asian countries has inevitably resulted in environmental degradation in the surrounding seas, and concern for the environment and its protection against pollutants is increasing. Identification of sources of contaminants and evaluation of current environmental status are essential to environmental pollution management, but relatively little has been done in the South China Sea (SCS). In order to investigate the abundance, distribution, and sources of Pb within the SCS, stable Pb isotopes and their ratios were employed to assess the contamination status and to differentiate between natural and anthropogenic origins of Pb in the surface sediments. The total Pb concentrations in sediments varied from 4.18 to 58.7 mg kg⁻¹, with an average concentration of 23.6 ± 8.9 mg kg⁻¹. The observed Pb isotope ratios varied from 18.039 to 19.211 for ²⁰⁶Pb/²⁰⁴Pb, 15.228 to 16.080 for ²⁰⁷Pb/²⁰⁴Pb, 37.786 to 39.951 for ²⁰⁸Pb/²⁰⁴Pb, 1.176 to 1.235 for ²⁰⁶Pb/²⁰⁷Pb, and 2.468 to 2.521 for ²⁰⁸Pb/²⁰⁷Pb. The majority of these ratios are similar to those reported for natural detrital materials. Combined with Pb enrichment factor values, our results show that Pb found within most of the SCS sediments was mainly derived from natural sources, and that there was not significant Pb pollution from anthropogenic sources before 1998. Further studies are needed to reconstruct deposition history and for trend analysis.     

Temporal evolution of lead isotope ratios in sediments of the Central Portuguese Margin: A fingerprint of human activities

Stable Pb isotope ratios (²⁰⁶Pb/²⁰⁷Pb, ²⁰⁸Pb/²⁰⁶Pb), ²¹⁰Pb, Pb, Al, Ca, Fe, Mn and Si concentrations were measured in 7 sediment cores from the west coast of the Iberian Peninsula to assess the Pb contamination throughout the last 200 years. Independently of their locations, all cores are characterized by increasing Pb/Al rends not related to grain-size changes. Conversely, decreasing trends of ²⁰⁶Pb/²⁰⁷Pb were found towards the present. This tendency suggest a change in Pb sources reflecting an increased proportion derived from anthropogenic activities. The highest anthropogenic Pb inventories for sediments younger than 1950s were found in the two shallowest cores of Cascais and Lisboa submarine canyons, reflecting the proximity of the Tagus estuary. Lead isotope signatures also help demonstrate that sediments contaminated with Pb are not constrained to estuarine–coastal areas and upper parts of submarine canyons, but are also to transferred to a lesser extent to deeper parts of the Portuguese Margin.     

Historical record of metal accumulation and lead source in the southeastern coastal region of Korea

Concentrations of heavy metals and Pb isotopes were measured in the 1-M HCl leaching fraction of core sediments spanning the last 400 years. This sedimentary record of pollution history in metal concentrations shows a good correlation with the increases in industrialization, urbanization, and energy consumption since 1901s. Notably, the Pb concentration and the ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb ratios were constant before the 1910s (16.7 μg/g, 0.844, and 2.098, respectively), whereas they increased steadily up to 21.9 μg/g, 0.848, and 2.101 after the 1910s. The correlations between Pb isotope ratios (²⁰⁶Pb, ²⁰⁷Pb, and ²⁰⁸Pb) showed different linear regression trends for core sediments before and after the 1910s, indicating differences in Pb sources. Our interpretation suggests that the source of anthropogenic Pb in Korean coastal region and the Yellow Sea shelf was presumed to be Chinese coals or ores, which have also played a major role as sources of atmospheric particulate Pb.     

Selenium in sediments and biota from estuaries of southwest England

Selenium concentrations have been measured in sediment, fucoid macroalgae and macroinvertebrates from four estuaries of SW England (Yealm, Plym, Looe, Fal). Sediment concentrations ranged from about 0.4 μg g⁻¹ in the Yealm to 1.49 μg g⁻¹ at one site in the Plym. Concentrations in Fucus vesiculosus (0.05–0.31 μg g⁻¹) and F. ceranoides (0.05–0.51 μg g⁻¹) were significantly lower than corresponding concentrations in sediment but there was no correlation between algal and sediment concentrations. Selenium concentrations in Littorina littorea (∼4 μg g⁻¹), Hediste diversicolor (2.82–12.68 μg g⁻¹), Arenicola marina (∼17 μg g⁻¹) and Scrobicularia plana (1.18–6.85 μg g⁻¹) were considerably higher than concentrations in macroalga or sediment, suggesting that Se is effectively accumulated from the diet. Although Se concentrations in some invertebrates exceed toxicity thresholds for the diet of predacious birds and fish, no specific evidence for Se toxicity exists in these estuaries.     

Refining the pre-industrial atmospheric Pb isotope evolution curve in Europe using an 8000 year old peat core from NW Spain

Pb pollution has existed for several millennia and remains relevant today. By using peat cores as environmental archives it is possible to reconstruct this long history on a regional scale. This is a significant contribution to the findings from ice core records, the only other archive recording purely atmospheric additions. Without information that allows linking and comparison between sites regionally, within Europe and elsewhere, our ability to make coherent global models of the natural Pb cycle, and anthropogenic forcing of this cycle, is limited. In this respect, the characteristics of the Pb pre-pollution aerosol (PPA) are important to define globally. We characterize for the first time a PPA in Southern Europe with [Pb] = 0.78 ± 0.86 μg g^− 1, net Pb accumulation rates of 0.032 ± 0.030 mg m^− 2 y^− 1 and a ²⁰⁶Pb / ²⁰⁷Pb signature of 1.25470 ± 0.02575. This PPA Pb isotope signature is more radiogenic than that found thus far in Western and Northern Europe. Spain is a historically important mining site. Using three-isotope plots and a pool of potential Pb isotope signatures, a detailed source appointment of both natural and anthropogenic Pb sources was made. We found evidence of Saharan aridification and its termination ∼4400 BP and/or agricultural signals and strong local control (from rock and soil) of the Pb PPA. Human impact is first recorded at 3210 BP but does not exceed 50% of deposited Pb until 3005 BP. Mines in SE Spain dominate early Pb pollution history at this site. During the rise of Roman rule, contributions come from mines in N, NW and SW Spain with no strong indication of other European mining activities. In Medieval and Industrial times local contributions to the peat bog are reduced.     

Trace elements in the sediments of a large Mediterranean marina (Port Camargue,France): Levels and contamination history

The study of trace elements (Cu, Zn, Pb, As, Hg) and butyltin concentrations in the sediments of Port Camargue enabled assessment of the levels and history of the contamination of the largest European marina linked with the use of antifouling paints. Surface sediments near the boat maintenance area were heavily contaminated with up to 1497 μg g⁻¹ of Cu, 475 μg g⁻¹ of Zn, 0.82 μg g⁻¹ of Hg, 94 μg g⁻¹ of Pb and over 10,000 ngSn g⁻¹ of tributyltin (TBT). High concentrations of Hg and TBT indicate ongoing sources of these elements despite the ban on their use as biocides in paints. Sediment cores provided records of contamination since 1969. The peak concentrations of As, Hg, Pb and TBT in the sediment profile reflect their presence on boat hulls when the marina was built at the end of the 1960s. Degradation of TBT in the sediments near the boat maintenance area is slow compared to other less contaminated area of the marina.     

Lead in blood and eggs of the sea turtle, Lepidochelys olivacea, from the Eastern Pacific: Concentration, isotopic composition and maternal transfer

Concentrations of lead were assessed in the sea turtle, Lepidochelys olivacea, from a nesting colony of the Eastern Pacific. Twenty-five female turtles were sampled and a total of 250 eggs were collected during the “arribada” event of the 2005-2006 season. Considering the nesting season, the maternal transfer of lead (Pb) via egg-laying, in terms of metal burden in whole body, was 0.5%. Pb concentrations (in dry weight) in blood (0.95 ± 0.18 μg g⁻¹) and egg samples (yolk, 0.80 ± 0.10 μg g⁻¹; albumen, 1.08 ± 0.20 μg g⁻¹; eggshell, 1.05 ± 0.20 μg g⁻¹) were comparable or even lower than those found in other sea turtles. The isotope ratios (²⁰⁶Pb/²⁰⁷Pb and ²⁰⁶Pb/²⁰⁸Pb) in blood (1.183 ± 0.0006 and 2.452 ± 0.0006, respectively) were comparable to that of natural Pb-bearing bedrock in Mexico (1.188 ± 0.005 and 2.455 ± 0.008, respectively). According to international norms of Pb, the health of this population and its habitats is acceptable for Pb and corresponds to basic levels of a nearly pristine environment.     

Lead concentrations and isotopes in aerosols from Xiamen, China

To investigate the magnitude and origin of lead (Pb) pollution in the atmosphere of Xiamen, China, 40 aerosol samples were collected from the coast of Xiamen from January to December 2003. All these samples were measured for Pb isotopic compositions (²⁰⁸Pb/²⁰⁶Pb = 2.10897 ± 0.00297, ²⁰⁷Pb/²⁰⁶Pb = 0.85767 ± 0.00159, n = 40) using a Multi-collector-Inductively Coupled Plasma Mass Spectrometer (MC-ICPMS). Thirty-five out of forty samples were also measured for Pb concentrations (79.1 ± 38.3 ng/m³, n = 35) by Atomic Absorption Spectroscopy (AAS). The results indicate that the Pb concentrations display significant seasonal variations while Pb isotopic ratios remain relatively constant. The Pb concentrations were high in January and February, abruptly decreased in March, remained relatively constant (but low) from April to August, and then gradually increased from September to December. This corresponds to the rainless climate in winter and rain scavenging in summer. The higher Pb concentration of Xiamen aerosols in winter and spring may be also caused by long-range transferred anthropogenic Pb during the northeastern monsoon seasons. Although the use of leaded gasoline in Xiamen was banned in 2000, our new data indicate that the Pb annual concentrations of aerosols in Xiamen increased about 12% when compared to the data measured between 1991 and 1993. Thus, Pb pollution in the atmosphere of Xiamen has not receded even after the phase-out of leaded gasoline. Our results further confirm the previous studies’ conclusion that the primary source of atmospheric Pb in China, especially in South China, is the vast combustion of lead-containing coal, not leaded gasoline.     

Occurrence and distribution of phthalate esters in riverine sediments from the Pearl River Delta region,South China

Sixty-eight sediment samples collected from Dongjiang River, Xijiang River, Beijiang River and Zhujiang River in the Pearl River Delta (PRD) region, Southern China, were analyzed for 16 phthalate esters (PAEs). PAEs were detected in all riverine sediments analyzed, which indicate that PAEs are ubiquitous environmental contaminants. The Σ₁₆PAEs concentrations in riverine sediments in the PRD region ranged from 0.567 to 47.3 μg g⁻¹ dry weight (dw), with the mean and median concentrations of 5.34 μg g⁻¹ dw and 2.15 μg g⁻¹ dw, respectively. Elevated PAEs concentrations in riverine sediments in the PRD region were found in the highly urbanized and industrialized areas. Of the 16 PAEs, diisobutyl phthalate (DiBP), di-n-butyl phthalate (DnBP) and di(2-ethylhexyl) phthalate (DEHP) dominated the PAEs, with the mean and median concentrations of 1.12 μg g⁻¹ dw, 0.420 μg g⁻¹ dw and 3.72 μg g⁻¹ dw, and 0.429 μg g⁻¹ dw, 0.152 μg g⁻¹ dw and 1.55 μg g⁻¹ dw, respectively, and accounted for 94.2–99.7% of the Σ₁₆PAEs concentrations. Influenced by local sources and the properties of PAEs, a gradient trend of concentrations and a fractionation of composition from more to less industrialized and urbanized areas were discovered. As compared to the results from other studies, the riverine sediments in the PRD region were severely contaminated with PAEs. Information about PAEs contamination status and its effect on the aquatic organisms in the PRD region may deserve further attention.     

Hydrocarbon composition and distribution in a coastal region under influence of oil production in northeast Brazil

Waters and sediments from the Potiguar Basin (NE Brazilian coast) were investigated for the presence and nature of polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons. The region receives treated produced waters through a submarine outfall system serving the industrial district. The total dispersed/dissolved concentrations in the water column ranged from 10-50 ng L⁻¹ for ∑16PAH and 5-10 μg L⁻¹ for total aliphatic hydrocarbons. In the sediments, hydrocarbon concentrations were low (0.5-10 ng g⁻¹for ∑16PAH and 0.01-5.0 μg g⁻¹ for total aliphatic hydrocarbons) and were consistent with the low organic carbon content of the local sandy sediments. These data indicate little and/or absence of anthropogenic influence on hydrocarbon distribution in water and sediment. Therefore, the measured values may be taken as background values for the region and can be used as future reference following new developments of the petroleum industry in the Potiguar Basin.     

Occurrence,distribution and partitioning of nonionic surfactants and pharmaceuticals in the urbanized Long Island Sound Estuary (NY)

This work deals with the environmental distribution of nonionic surfactants (nonylphenol and alcohol ethoxylates), their metabolites (NP, nonylphenol; NPEC, nonylphenol ethoxycarboxylates; and PEG, polyethylene glycols) and a selection of 64 pharmaceuticals in the Long Island Sound (LIS) Estuary which receives important sewage discharges from New York City (NYC). Most target compounds were efficiently removed (>95%) in one wastewater treatment plant monitored, with the exception of NPEC and some specific drugs (e.g., hydrochlorothiazide). Concentrations of surfactants (1.4–4.5 μg L⁻¹) and pharmaceuticals (0.1–0.3 μg L⁻¹) in seawater were influenced by tides and sampling depth, consistent with salinity differences. Surfactants levels in suspended solids samples were higher than 1 μg g⁻¹, whereas only most hydrophobic or positively charged pharmaceuticals could be found (e.g., tamoxifen, clarithromycin). Maximum levels of target compounds in LIS sediments (PEG at highest concentrations, 2.8 μg g⁻¹) were measured nearest NYC, sharply decreasing with distance from major sewage inputs.     

In situ heavy metals (copper, lead and cadmium) in different plankton compartments and suspended particulate matter in two coupled Mediterranean coastal ecosystems (Toulon Bay, France)

We monitored the concentrations of copper, lead and cadmium in seawater, in suspended particulate matter (SPM) and in bacteria, phyto- and zooplankton communities separated from abiogenic particles, over a one year cycle in two coupled Mediterranean coastal ecosystems (Little Bay (LiB) and Large Bay (LaB)). Metals were present in seawater in the order Cu > Pb > Cd in both bays and showed important variations within the same month than among months. In LiB, their concentrations were between 0.62 and 2.82 μg Cu l⁻¹, 0.16 and 19 μg Pb l⁻¹ and 0.007 and 0.14 μg Cd l⁻¹, respectively, whereas in LaB, they were between 0.23 and 2.11 μg Cu l⁻¹, 0.09 and 0.76 μg Pb l⁻¹ and not detected and 0.65 μg Cd l⁻¹. SPM play an important role on metal adsorption, especially for copper. Bioaccumulation factors showed that bacteria and phytoplankton accumulate metals whereas zooplankton tends to biodiminish them in the plankton food web.     

The application of lead isotope ratios in the Antarctic macroalga Iridaea cordata as a contaminant monitoring tool

Lead (Pb) isotope ratios were measured in the marine macroalga Iridaea cordata collected from four locations in the Windmill Islands, East Antarctica. Based on the masses of thalli collected, samples analysed in this study were likely to be a mixture of one and two year old thalli. For a sample of thalli of various ages (<12 months to 2 years old) from the same site there was no apparent variation in Pb concentration or Pb isotope ratio with thallus mass/age, indicating that contaminant sources had been constant over the lifetime of the thalli sampled. I.cordata samples close to the Thala Valley waste disposal site (Brown Bay Inner) near the Australian Station, Casey, displayed isotopic signatures (²⁰⁸Pb/²⁰⁴Pb 35.99; ²⁰⁶Pb/²⁰⁷Pb 1.066; n = 3; average values shown) trending towards that possessed by major Australian Pb sources (Broken Hill and Mt Isa, ²⁰⁸Pb/²⁰⁴Pb 35.60; ²⁰⁶Pb/²⁰⁷Pb 1.041) suggesting that these samples had been exposed to anthropogenic Pb originating from the Thala Valley waste disposal site. Material collected hundreds of metres from the tip location at Brown Bay Outer had isotopic values (²⁰⁸Pb/²⁰⁴Pb 36.32; ²⁰⁶Pb/²⁰⁷Pb 1.088; n = 10) intermediate between Brown Bay Inner and sites further from the contaminant source at Sparkes Bay and Wilkes (²⁰⁸Pb/²⁰⁴Pb 36.46; ²⁰⁶Pb/²⁰⁷Pb 1.094; n = 4) showing that contaminant transport was predominantly restricted to Brown Bay Inner. This study demonstrates that the isotope ratios of Pb in marine macroalgae can provide valuable information as to the origin and extent of heavy metal flux in a marine environment.     

Mantle plume heterogeneity versus shallow-level interactions: A case study,the São Nicolau Island,Cape Verde archipelago

We present new Sr–Nd–Pb isotopic data, as well as major- and trace-element concentrations, for 19 basaltic samples from São Nicolau Island, Cape Verde archipelago. Fine-scale study of the island argues in favor of mixing between four endmembers to explain isotopic variations of collected samples: 1) a radiogenic endmember (⁸⁷Sr/⁸⁶Sr ~ 0.7034; ¹⁴³Nd/¹⁴⁴Nd ~ 0.51285; ²⁰⁶Pb/²⁰⁴Pb ~ 20.0; ²⁰⁷Pb/²⁰⁴Pb ~ 15.65; ²⁰⁸Pb/²⁰⁴Pb ~ 39.8) representative of the Cape Verde plume deep source; 2) an unradiogenic endmember having isotopic compositions resembling those of Atlantic MORB dredged at the same latitude; 3) a low Sr–high Nd and Pb endmember identified as the Jurassic MORB basement of the archipelago; and 4) São Vicente-like Cape Verde carbonatites. Compositional and isotopic results show that most of the measured variations can be related to mixing of plume-derived melts with shallow-level reservoirs. Therefore the source heterogeneity of the Cape Verde plume is much smaller than the one sampled in basaltic samples. This observation illustrates how caution is required when interpreting global OIB data in terms of mantle topology without filtering from the contribution of shallow-level reservoirs.     

Stable Pb isotope ratios in aerosols, precipitation, and size-fractionated particulate matter in the Gulf of Maine, Scotian Shelf, and Labrador Sea

Measurements of Pb isotopes in aerosols, precipitation, and size-fractionated particulate matter from the Gulf of Maine, Scotian Shelf and Labrador Sea are used to investigate the source of Pb. The ²⁰⁶Pb/²⁰⁷Pb ratio in aerosols and precipitation collected at New Castle, NH suggests that anthropogenic Pb is a mixture of US and Canadian sources. ²⁰⁶Pb/²⁰⁷Pb ratios in >53 μm particulate matter from the Gulf of Maine and Scotian Shelf slope waters are consistent with contaminant Pb inputs predominantly from US and Canadian sources, while in shelf waters ²⁰⁶Pb/²⁰⁷Pb ratios in >0.4 μm and >53 μm particles are consistent with a mixture of US and Canadian sources, as well as Pb associated with resuspended surface sediment. ²⁰⁶Pb/²⁰⁷Pb ratios in particulate matter (>0.4 μm, 10-53 μm, and >53 μm) from Labrador Sea surface waters range from 1.165 to 1.211 and are a mixture of Pb derived from ore compositions consistent with Broken Hill, Australia and southeast Missouri, US sources.     

Benthic fluxes of dissolved inorganic carbon in the Tinto–Odiel system (SW of Spain)

The benthic fluxes (diffusive and with chambers) of dissolved inorganic carbon (DIC), dissolved oxygen (DO) and total alkalinity (TA) have been calculated in summertime in the estuary system formed by the mouths of the Tinto and Odiel rivers (SW of Spain). An increase of DIC in interstitial water with depth was found for all stations showing values of up to 28 mM at a depth of 5 cm. The diffusive fluxes of DIC and TA obtained ranging between 1.8–7.8 and 1.5–7.3 mmol m⁻² d⁻¹, respectively. These intervals are in agreement with those found for other coastal systems. Considering the plots of DIC vs. alkalinity (ΔDIC/ΔTA) in the first 30 cm of interstitial water, it was deduced that sulphate reduction and the oxidation of sulphides seem to have special relevance in the sediments of the stations studied. The benthic fluxes of inorganic carbon and DO measured by benthic chambers were variable, presenting elevated values (309–433 mmol DIC m⁻² d⁻¹ and 50–120 mmol DO m⁻² d⁻¹). The most elevated fluxes of DIC were seen at the stations with high anthropogenic influence (close to populated areas and industrial discharges). A great proportion of these fluxes are due to CaCO₃ dissolution processes, which constitute an estimated 49% of total DIC flux. DIC and DO benthic flux quotients were far in excess of unity, indicating the significance processes of anaerobic degradation of organic material at the stations studied.     

Baseline heavy metals and metalloid values in blood of loggerhead turtles (Caretta caretta) from Baja California Sur, Mexico

Environmental pollution due to heavy metals is having an increased impact on marine wildlife accentuated by anthropogenic changes in the planet including overfishing, agricultural runoff and marine emerging infectious diseases. Sea turtles are considered sentinels of ecological health in marine ecosystems. The objective of this study was to determine baseline concentrations of zinc, cadmium, copper, nickel, selenium, manganese, mercury and lead in blood of 22 clinically healthy, loggerhead turtles (Caretta caretta), captured for several reasons in Puerto López Mateos, Baja California Sur, Mexico. Zinc was the most prevalent metal in blood (41.89 μg g⁻¹), followed by Selenium (10.92 μg g⁻¹). The mean concentration of toxic metal Cadmium was 6.12 μg g⁻¹ and 1.01 μg g⁻¹ respectively. Mean concentrations of metals followed this pattern: Zn > Se > Ni > Cu > Mn > Cd > Pb and Hg. We can conclude that blood is an excellent tissue to measure in relatively non-invasive way baseline values of heavy metals in Caretta caretta.     

Distribution of rare earth elements in marine sediments from the Strait of Sicily (western Mediterranean Sea): evidence of phosphogypsum waste contamination

Concentrations of rare earth elements (REE), Y, Th and Sc were recently determined in marine sediments collected using a box corer along two onshore-offshore transects located in the Strait of Sicily (Mediterranean Sea). The REE + Y were enriched in offshore fine-grained sediments where clay minerals are abundant, whereas the REE + Y contents were lower in onshore coarse-grained sediments with high carbonate fractions. Considering this distribution trend, the onshore sediments in front of the southwestern Sicilian coast represent an anomaly with high REE + Y concentrations (mean value 163.4 μg g⁻¹) associated to high Th concentrations (mean value 7.9 μg g⁻¹). Plot of shale-normalized REE + Y data of these coastal sediments showed Middle REE enrichments relative to Light REE and Heavy REE, manifested by a convexity around Sm-Gd-Eu elements. These anomalies in the fractionation patterns of the coastal sediments were attributed to phosphogypsum-contaminated effluents from an industrial plant, located in the southern Sicilian coast.     

Anthropogenic organic matter inputs indicated by sedimentary fecal steroids in a large South American tropical estuary (Paranaguá estuarine system, Brazil)

Urban sewage is considered one of the most important sources of marine pollution in South America, because most coastal cities do not have proper facilities to treat and dispose of sewage. The Paranaguá estuarine system is an important estuarine environment of the South American coast where fishing, urban and tourist activities, industries and the main Brazilian grain shipping port are potential sources of pollution in this area. The anthropogenic input of sedimentary organic matter, represented by sewage contribution, was evaluated by fecal steroid concentrations. The coprostanol levels were comparatively low (<0.10 μg g⁻¹), except at the sites close to Paranaguá city, where the coprostanol concentration reached 2.22 μg g⁻¹ showing strong sewage contamination. Fecal steroid levels were comparable to the lower to midrange concentrations reported for coastal sediments worldwide. The results of this work demonstrated that sewage pollution can be considered a problem for a small part of the Paranaguá estuary.