Eliete Zanardi-Lamardo

Sources and distribution of polycyclic aromatic hydrocarbons in a an urbanized tropical estuary and adjacent shelf, Northeast of Brazil

Located in Northeastern Brazil, the Capibaribe Estuarine System is an important ecosystem that supplies food and protection for nursery of several species with ecological and economic importance. It is located inside an urbanized area, receives untreated domestic and industrial effluents, and houses some marinas and the Harbor of Recife, which are very important to national and international communities. The distribution and sources of PAHs were investigated in sediments from CES and adjacent shelf. Total PAH concentrations ranged from non-detectable to 497.6 μg g(-1). Pyrolytic sources predominated in most of sites, but petrogenic PAHs were also recorded. The concentration decrease of PAHs toward adjacent shelf suggests that the main source of these compounds is in the upper portion of estuary, where there is an intense discharge of sewage, but atmospheric input also seems to be relevant to the area. The results reinforce the important role of an estuary in contaminant retention.

Petroleum hydrocarbons in water from a Brazilian tropical estuary facing industrial and port development.

A fast paced industrial and port development has occurred at Suape Estuary, Northeast Brazil, but no information about hydrocarbon concentrations in water is available to this area. Considering that, the contamination level of Suape was determined by UV-Fluorescence in terms of dissolved and/or dispersed petroleum hydrocarbons (DDPHs), during wet and dry seasons. DDPHs ranged between 0.05 and 4.59 μg L(-1) Carmópolis oil equivalents and 0.01-1.39 μg L(-1) chrysene equivalents, indicating DDPHs close to a baseline contamination level. Some relatively high concentrations (>1 μg L(-1)) were probably associated with shipyard operations (hull paintings and ship docking), pollutants remobilization by dredging operations, occasional industrial discharges and oil derivatives released by vessels. DDPHs concentrations were lower in the wet season suggesting that the increased dilution rates caused by rainfall dominated upon the wet deposition of atmospheric combustion-derived PAHs process. Results in this study may be used as baseline to further studies in this area.

Bioconcentration of phenanthrene and metabolites in bile and behavioral alterations in the tropical estuarine guppy Poecilia vivipara

Quantification of polycyclic aromatic hydrocarbon (PAH) metabolites in fish bile is widely used to evaluate levels of internal PAH contamination in fish, whereas behavioral effects are deemed important to address potential risks to fish populations. The estuarine guppy Poecilia vivipara was exposed for 96h to waterborne phenanthrene at concentrations of 10, 50, 200 and 500μgL(-1). Phenanthrene and metabolites in bile were analyzed by fixed fluorescence at 260/380nm (excitation/emission) wavelengths. Phenanthrene increased in the bile of exposed fish in a dose-dependent pattern, and log bile bioconcentration factors ranged from 4.3 to 3.9 at 10 and 500μgL(-1) phenanthrene, respectively, values that are similar to predicted bioconcentration factors based on phenanthrene Kow. Swimming resistance index was reduced to 81% of control values at 500μgL(-1). Alteration of swimming speed was non monotonic, with a significant speed increase relative to control fish in treatments 50 and 200μgL(-1) phenanthrene, respectively, followed by a speed decrease in fish exposed to 500μgL(-1). However, swimming trajectories of fish exposed to 50, 200 and 500μgL(-1) was altered by the development of a repetitive circular swimming behavior, in contrast to the controls that explored the entire experimental arena. This change in swimming patterns apparently explains the reduction in prey capture rates at 200μgL(-1) phenanthrene. This study provides important information enabling the use of the estuarine guppy P. vivipara to monitor PAH metabolites in bile and its bioconcentration, linking internal exposure with ecologically relevant behavioral effects in the species.

Hydrocarbons in sediments along a tropical estuary-shelf transition area: Sources and spatial distribution

Estuaries generally act as sediment traps and may retain a range of contaminants associated to this matrix. Aliphatic hydrocarbons (AHs) were investigated in Capibaribe Estuarine System and adjacent shelf, Northeast of Brazil, to evaluate the contamination and to better understand its functionality related to the coast. Fourteen sediment samples were analyzed, using gas chromatography with flame ionization detection. Total AHs concentrations ranged from 7.5 to 190.3μgg-1 and n-alkanes ranged from below detection limit (<DL) to 9.47μgg-1. The highest concentrations were in the upper portion of the estuary, which receives domestic and industrial effluents. The observed UCM and other geochemical markers, indicated contamination by petroleum hydrocarbons. The concentration decrease (about 90%) towards the adjacent shelf suggested an estuarine high retention capacity but dilution and degradation processes cannot be neglected. Similar AHs characteristics reported in sediments from the adjacent shelf suggested that this system may also export contaminants.

THE FATE OF AN OIL SPILL IN SÃO SEBASTIÃO CHANNEL: A CASE STUDY

An oil pipeline ruptured in May 1994 and 2 700 tons of crude oil leaked into the Sao Sebastiao Channel, affecting several neighboring areas. A program for the monitoring of hydrocarbons in sediments, using the gas chromatography / flame ionization detector methodology, was being undertaken in the area at the time. The data obtained were compared to those of samples collected after the accident to determine the fate of the oil spilled and ascertain its contribution to the environment. The earlier results showed that hydrocarbons were introduced from two different sources: biogenic, mainly from terrestrial plants, and anthropogenic, as oil, in sewage and from shipping. The later data indicated that the site closest to the pipeline rupture had been the most affected. Following that, two stations located at the north entrance of the channel presented the highest n-alkane concentrations, suggesting that the northeasterly wind-driven currents had carried the oil northward. Seven months later, one of these stations, a high-energy site, showed some signs of recovery, but this process was not observed at the other, which seemed to be a low-energy site. In conclusion, the data showed that the aliphatic hydrocarbon analyses were powerful tools for the assessment of the fate of the oil spill and that the northern part of the Sao Sebastiao Channel is more subject to the effects of oil spills.

Sources and distribution of aromatic hydrocarbons in a tropical marine protected area estuary under influence of sugarcane cultivation

Goiana estuary is a well preserved marine protected area (MPA) located on the northeastern coast of Brazil. Despite its current state, human activities in the watershed represent a potential threat to long term local preservation. Dissolved/dispersed aromatic hydrocarbons and polycyclic aromatic hydrocarbons (PAHs) were investigated in water and sediments across the estuarine salt gradient. Concentration of aromatic hydrocarbons was low in all samples. According to results, aromatic hydrocarbons are associated to suspended particulate matter (SPM) carried to the estuary by river waters. An estuarine turbidity maximum (ETM) was identified in the upper estuary, indicating that both sediments and contaminants are trapped prior to an occasional export to the adjacent sea. PAHs distribution in sediments were associated with organic matter and mud content. Diagnostic ratios indicated pyrolytic processes as the main local source of PAHs that are probably associated with sugarcane burning and combustion engines. Low PAH concentrations probably do not cause adverse biological effects to the local biota although their presence indicate anthropogenic contamination and pressure on the Goiana estuary MPA.

Assessment of organotins and imposex in two estuaries of the northeastern Brazilian coast

Butyltin compounds (BTs) were used worldwide, especially because of their properties as biocides. Due to its high toxicity, the use of tributyltin (TBT) in antifouling paints has been prohibited in most countries. The occurrence and impact of BTs were assessed in surface sediments and in Stramonita rustica populations of two tropical estuaries that host major ports in northeastern Brazil. ΣBT concentrations ranged from <LOQ to 542ngSng-1 dry weight in sediments while imposex was not observed in S. rustica. This is in contrast to previous studies that reported high incidence of imposex at the same sites. Butyltin degradation index indicates recent input of TBT at levels that might trigger imposex in gastropod species more sensitive than S. rustica. These results emphasize the need of more rigorous controls by local authorities since Brazil has restricted the use of TBT-based antifouling paints.

Aquatic organic matter: Classification and interaction with organic microcontaminants

Organic matter (OM) in aquatic system is originated from autochthonous and allochthonous natural sources as well as anthropogenic inputs, and can be found in dissolved, particulate or colloidal form. According to the type/composition, OM can be divided in non-humic substances (NHS) or humic substances (HS). The present review focuses on the main groups that constitute the NHS (carbohydrates, proteins, lipids, and lignin) and their role as chemical biomarkers, as well as the main characteristics of HS are presented. HS functions, properties and mechanisms are discussed, in addition to their association to the fate, bioavailability, and toxicity of organic microcontaminants in the aquatic systems. Despite the growing diversity and potential impacts of organic microcontaminants to the aquatic environment, limited information is available about their association with OM. A protective effect is, however, normally seen since the presence of OM (HS mainly) may reduce bioavailability and, consequently, the concentration of organic microcontaminants within the organism. It may also affect the toxicity by either absorbing ultraviolet radiation incidence and, then, reducing the formation of phototoxic compounds, or by increasing the oxygen reactive species and, thus, affecting the decomposition of natural and anthropogenic organic compounds. In addition, the outcome data is hard to compare since each study follows unique experimental protocols. The often use of commercial humic acid (Aldrich) as a generic source of OM in studies can also hinder comparisons since differences in composition makes this type of OM not representative of any aquatic environment. Thus, the current challenge is find out how this clear fragmentation can be overcome.