Simultaneous measurements of ammonia and nitric acid in ambient air at Agra (27°10′N and 78°05′E) (India)

Simultaneous measurements of ammonia and nitric acid in ambient air were conducted at Dayalbagh, Agra using the mist chamber technique. The sampling site is located near a cattle shed. A total of 120 samples were collected during the period July–September and November–February (1997–1998). Sampling was performed during six different times a day. Gas-phase HNO₃ was estimated as NO₃⁻ using ion chromatographic technique while ammonia was determined colorimetrically as NH₄⁺ using indophenol blue method. The mean levels of NH₃ and HNO₃ for the entire data set were 16.3±2.8 and 1.6±1.4 ppbv, respectively. In the monsoon, mean values for NH₃ and HNO₃ averaged to 16.4±3.5 and 0.9±0.7 ppbv while the winter means were 11.8±4.4 and 2.1±1.2 ppbv, respectively. Concentration of both the species (NH₃ and HNO₃) did not show any significant diurnal behaviour in both the seasons. However, concentration of both NH₃ and HNO₃ were lower at dawn than the previous night's value. This has been ascribed to their removal through dew. Concentrations of HNO₃ are observed to increase during the daytime, consistent with its formation by photochemical reactions. Nitric acid and ammonia concentrations show a significant seasonal variation. Levels of HNO₃ are higher in winter but lower in monsoon, while ammonia shows a reverse trend with higher monsoon and lower winter values. Observed trends in nitric acid and ammonia concentration are due to seasonal variation in emission sources, chemistry and meteorology. Gaseous ammonia and nitric acid are in equilibrium with NH₄NO₃ (solid or aqueous) in the atmosphere. The existence of this equilibrium was examined from simultaneous measurements of NH₃ and HNO₃ in the ambient air. It is found that for the monsoon data, measured concentrations are qualitatively below the predicted equilibrium value, while in the winter, concentration product ([NH₃] [HNO₃]) lies consistently above the predicted values. These deviations may be explained due to local sources of both [NH₃] and [HNO₃], presence of coarse nitrate particles and low-temperature and high-humidity conditions.     

The composition of individual aerosol particle in the troposphere and stratosphere over Xianghe (39.45°N, 117.0°E), China

A balloon observation was carried out on 22 August in 1993 from Xianghe Scientific Balloon Base (39.75°N, 117.0°E) near Beijing in China. Individual aerosol particles in the five samples collected in the troposphere and lower stratosphere were analyzed by using a transmission electron microscope equipped with an energy-dispersive X-ray (EDX) analyzer. Types of particles were classified by the quantitative EDX analysis and particle morphology. Following results were obtained by the analyses of aerosol particles in the radius range of 0.1–0.5 μm: (1) Sulfate particles were dominant (80%) in aerosol particles collected between 4 and 6 km altitude. (2) Sulfuric acid particles were present in 74% of particles at ∼8 km altitude, 91% at 11 km, 95% at 17 km and 88% at 21.2 km. (3) “S-rich” particles with K were collected both in the troposphere and lower stratosphere. It was considered that the particles containing K found at ∼5, ∼8 km altitude could originate from burning processes in the continent including the Tibetan plateau and be transported to the middle troposphere. (4) Sulfuric acid particles with Fe were present in 20–30% of sulfuric acid particles in the lower stratosphere. (5) Particles mainly composed of minerals were present in 6, 11% of particles at ∼5, ∼8 km, indicating the vertical transport to the upper troposphere. (6) Mineral particles which contain sulfuric acid and sulfate suggest the formation of sulfuric acid and sulfate on mineral particles by heterogeneous processes in the troposphere. (7) Sea-salt particles with and without minerals were collected in the troposphere and lower stratosphere, suggesting the vertical transport by convective clouds.     

The ‘Storm of the Century’ (December 1999) and the accidental escape of Siberian sturgeons (Acipenser baerii) into the Gironde estuary (Southwest France)

GOAL, SCOPE AND BACKGROUND: The Gironde estuary is considered as a reference ecosystem with a large fish assemblage (75 species) and the presence of eleven diadromous species. However, geochemical studies and biomonitoring using oysters have shown high metal pollution levels. During the December 1999 hurricane, more than 5,000 young Siberian sturgeons (Acipenser baerii) accidentally escaped from a fish farm into the estuary, where this species had not been present until then. METHODS: In 2002/2003, thirteen sturgeons were collected from the estuary and twelve were obtained from the fish farm, from the same initial batch. Analysis of five metals (cadmium, zinc, copper, lead, mercury) measured in the gills, muscle, liver and kidneys, revealed significantly higher levels of cadmium, lead and mercury in the sturgeon collected from the estuary compared with those from the fish farm. RESULTS AND DISCUSSION: Metal analysis of the stomach contents of fish collected from the estuary and artificial food used in the fish farm indicated that dietary exposure might account for the differences observed. Nevertheless, metal concentrations in sturgeons that had spent about three years in the Gironde estuary may be considered low when compared with other species (mullets, eels) or with data in the literature regarding concentrations able to induce structural and functional perturbations in fish. As the introduced Siberian sturgeons live in the same place and feed on the same prey as the juveniles of the endangered A. sturio, our results indicate in the short-term that this strictly protected species does not appear to be much affected by the polymetallic pollution in the Gironde estuary. Marked differences in the concentrations of three metals (Cd, Pb, Hg) were established in four organs (gills, liver, skeletal muscle, kidneys) of Siberian sturgeons between specimens that had accidentally escaped into the Gironde estuary (France) during the December 1999 hurricane and were collected in March/June 2003 and specimens from the same initial batch at the fish farm. RECOMMENDATIONS AND PERSPECTIVES: Based on these results, a programme will be set up, with sampling campaigns carried out in the estuary every two years, with systematic monitoring of age in order to check the origin of individuals, in conjunction with sampling of sturgeon from the fish farm. This programme will complement other studies on several biological species representative of the main trophic levels in the estuary, especially the plankton component, benthic macroinvertebrates and oysters.     

Aromatic hydrocarbons at urban,sub-urban,rural (8°52′N; 67°19′W) and remote sites in Venezuela

Using the novel on-line proton transfer reaction mass spectrometry (PTR-MS) technique, atmospheric concentrations of benzene, toluene, xylenes, and C₉-benzenes were measured in Caracas (urban), Altos de Pipe (sub-urban), Calabozo (rural) and Parupa (remote), during various campaigns in 1999 and 2000.Average daytime mixing ratios measured in Caracas are 1.1, 3.2, 3.7, and 2.7 nmol/mol for benzene, toluene, xylenes, and C₉-benzenes. At the sub-urban site, located only few km from Caracas, relatively low levels (∼20% of the levels measured in Caracas) of these aromatic hydrocarbons were observed.At the rural site during the dry season, higher concentrations of benzene (0.15 nmol/mol) were recorded, whereas those of toluene (0.08 nmol/mol) were lower during that time. The aromatic hydrocarbon ratios in the wet season (benzene: 0.08 nmol/mol; toluene: 0.09 nmol/mol) are consistent with an aged urban plume, whereas biomass burning emissions dominate during the dry season. From rural and urban [benzene]/[toluene] ratios a mean HO concentration of 2.6×10⁶ molecules/cm³ was estimated during the wet season. This value must be considered an overestimate because it does not account for background concentrations which are likely for benzene and toluene.At the remote “La Gran Sabana” region (Parupa) very low mixing ratios (0.031 and 0.015 nmol/mol for benzene and toluene) are showing the pristine region to be unaffected by local sources. From the [benzene]/[toluene] ratio we deduced, that “urban” air arriving from the coastline (350 km) is likely mixed with air containing some background of benzene and toluene.Urban emissions (automobiles) should be the major source of aromatic compounds, however, during the dry season biomass burning seems to make an important contribution.     

Diurnal variation in the concentration of α- and β-pinene in the landes forest (France)

The study deals with the identification and the determination of the main monoterpenes (α- and β-pinene) released by the pines in the Landes Forest in France. The measurements were taken after preconcentration using TENAX-GC and thermal desorption. The diurnal variation of atmospheric concentration of α- and β-pinene is established; it is less than 0.5 ppbV in the daytime and varies from 2 to 4 ppbV in the night-time. These variations are explained by the fact that the photochemical reactions and the turbulence phenomena to which the terpenes are exposed change quite radically from day to night. The terpene concentration, higher at 5 m than at 25 m, would seem to confirm the existence of a terpene source at ground level.     

Spatial and temporal variability of ²¹⁰Po and ²¹⁰Pb in mussels (Mytilus galloprovincialis) at the Turkish coast of the Aegean Sea

In this study, the activity concentrations of ²¹⁰Po and ²¹⁰Pb were determined in mussel samples (Mytilus galloprovincialis) collected from the Turkish coast of the Aegean Sea. The samples were collected seasonally for a period of two years (2004-2006) at six coastal stations (Çanakkale, Dikili, Foça, Çe?me, Didim, Bodrum). Mussels were separated into several groups according to their size (1-4, 4-6, >6 cm). The results showed that ²¹⁰Po concentrations in mussels varied between 53 ± 4 and 1960 ± 60 Bq kg⁻¹ dw. The highest activity ²¹⁰Po concentrations were determined in winter samples of mussels with a shell length of 4-6 cm from Didim. In general, it was observed that the ²¹⁰Pb concentration levels in mussels were lower than ²¹⁰Po concentrations. The ²¹⁰Po/²¹⁰Pb activity concentration ratios exceeded unity for all mussel samples and averaged 26.0. The inter-site differences seen in ²¹⁰Po concentrations can be due to both the natural background levels of sites and industrial activities.     

Methanol measurements in the lower troposphere near Innsbruck (047°16′N; 011°24′E), Austria

Diurnal variations on a time scale of minutes of the mixing ratios of methanol were measured using proton transfer reaction mass spectrometry (PTR-MS) technique during 67 days throughout the time span from November 1996 to July 1998 together with benzene and other volatile organic compounds at the western outskirts of Innsbruck, Austria. Comparison with the course of the mixing ratio of benzene, which served as marker for traffic emissions, as well as the observation of a seasonal variation allowed to distinguish between different sources for methanol release into the troposphere. Strong evidence for methanol removal via deposition on dew-wetted surfaces is obtained from the comparison of meteorological data with methanol mixing ratios. The mean volume mixing ratio of total methanol was 7.5 nmol mol⁻¹. Mixing ratios ranged from 0.03 up to 45 nmol mol⁻¹.     

Inhomogeneities and trends in the surface ozone record (1988–1996) at Jungfraujoch in the Swiss Alps

Ozone data at the Jungfraujoch Observatory (3580 m asl) in the Swiss Alps have been recorded continuously since 1986 in the framework of the Swiss National Air Pollution Monitoring Network (NABEL), operated by the Swiss Federal Laboratories for Materials Testing and Research (EMPA). The long-term ozone record (1988–1996) was examined with regard to potential inhomogeneities using Zugspitze (2960 m asl), a neighbouring alpine site in Germany, as a reference site. The Alexandersson test (for shift) and the Easterling–Peterson test (for trend and shift) were applied to a difference times series, calculated from monthly ozone means at Jungfraujoch and Zugspitze. The Alexandersson test revealed a significant shift discontinuity in November 1989 and the Easterling–Peterson test a trend discontinuity in September 1991. It is assumed that the shift discontinuity may be related to an instrument change, but there is not firm evidence due to lack of detailed information from the instrumental history in the earlier years of the ozone record at Jungfraujoch. Monthly ozone means at Davos (1640 m asl) in eastern Switzerland indicate that part of the trend discontinuity in September 1991 may be of natural origin. Adjustment of the monthly ozone means at Jungfraujoch for the observed shift discontinuity removed the inhomogeneity in November 1989, and reduced the trend discontinuity by a factor of 4.8. A trend analysis on both adjusted (homogenised) and unadjusted monthly ozone means (1988–1996) at Jungfraujoch showed no statistically significant linear trend. The boundaries encompassing the true linear trend are indicated by two linear regression calculations on both adjusted and unadjusted data. Trends in the cold season are positive albeit not significant. The only statistically significant trends are found in October, December, and February for the adjusted data.     

Sources and concentrations of gaseous and particulate reduced nitrogen in the city of Münster (Germany)

Atmospheric ammonia mixing ratios and the main inorganic ions NH₄⁺, NO₃⁻ and SO₄²⁻ of size-resolved particles in the range from 0.05 to 10 μm were measured at an urban site in Münster, Germany. High mixing ratios of ammonia with a median of 5.2 ppb and a maximum of 50 ppb were detected. The mass fraction of submicron particles was much higher during the day than at night. At night, a greater particle mass and an increased presence of particulate nitrate was measured. Recurring patterns of particle distribution were distinguished and their characteristics analysed. In half of the measurements, the accumulation mode was clearly dominating, which is an indication of aged aerosol. In some measurements, higher concentrations of fine particles were found indicating particle formation. In these cases, a smaller particle mass and about four times greater ratios of ammonia versus ammonium concentrations were observed. These data show that ammonia contributes considerably to the formation of secondary particulate material.     

The sea–air exchange of mercury (Hg) in the marine boundary layer of the Augusta basin (southern Italy): Concentrations and evasion flux

The first attempt to systematically investigate the atmospheric mercury (Hg) in the MBL of the Augusta basin (SE Sicily, Italy) has been undertaken. In the past the basin was the receptor for Hg from an intense industrial activity which contaminated the bottom sediments of the Bay, making this area a potential source of pollution for the surrounding Mediterranean. Three oceanographic cruises have been thus performed in the basin during the winter and summer 2011/2012, where we estimated averaged Hg_atm concentrations of about 1.5 ± 0.4 (range 0.9–3.1) and 2.1 ± 0.98 (range 1.1–3.1) ng m⁻³ for the two seasons, respectively. These data are somewhat higher than the background Hg_atm value measured over the land (range 1.1 ± 0.3 ng m⁻³) at downtown Augusta, while are similar to those detected in other polluted regions elsewhere. Hg evasion fluxes estimated at the sea/air interface over the Bay range from 3.6 ± 0.3 (unpolluted site) to 72 ± 0.1 (polluted site of the basin) ng m⁻² h⁻¹. By extending these measurements to the entire area of the Augusta basin (∼23.5 km²), we calculated a total sea–air Hg evasion flux of about 9.7 ± 0.1 g d⁻¹ (∼0.004 t yr⁻¹), accounting for ∼0.0002% of the global Hg oceanic evasion (2000 t yr⁻¹). The new proposed data set offers a unique and original study on the potential outflow of Hg from the sea–air interface at the basin, and it represents an important step for a better comprehension of the processes occurring in the marine biogeochemical cycle of this element.     

The toxic effects of neem extract and azadirachtin on the brown planthopper, Nilaparvata lugens (Stål) (BPH) (Homoptera: Delphacidae)

Extracts of neem (Azadirachta indica A. Juss) are used in the developing world for many purposes including management of agricultural insect pests. The effects of different neem extracts (aqueous (NSKEaq), ethanol (NSKEeth) and hexane (NSKEhex)) on mortality, survival and weight of the brown planthopper, Nilaparvata lugens (St?l) (BPH) (Homoptera: Delphacidae) third and fourth nymphal instars were investigated. When fed rice plants treated with neem derivatives in bioassays, the survival of BPH nymphs is affected. Comparisons were made with the pure neem limonoid, azadirachtin (AZA) to ascertain its role as a compound responsible for these effects. AZA was most potent in all experiments and produced almost 100% nymphal mortality at 0.5 ppm and higher concentrations. When higher concentrations were applied, the effects appeared shortly after treatment and mortality was higher. Many insects died after remaining inactive for several days or during prolonged moulting. At lower concentrations, if moulting was achieved, disturbed growth and abnormalities were then likely to occur in the moulting process. Nymphs that were chronically exposed to neem extract showed a reduction in weight (45-60%). The results clearly indicate the simple NSKE (aqueous, ethanolic or both), containing low concentrations of AZA, can be used effectively to inhibit the growth and survival of BPH.     

Current State of the Altai Glaciers (Russia) and Trends Over the Period of Instrumental Observations 1952–2008

Results of research into climate and glacier dynamics in the Altai Mountains (Russia) over the period of instrumental observations (1952–2008) are presented in this article. About 1030 glaciers with a total area of 805 km² and volume of 42.5 km³ have been recorded in the Altai Region. The average summer air temperature in different regions of the Altai has increased during the study period from about 0.2°C (Aktru) to 1.1°C (Akkem). The annual atmospheric precipitation rate has also increased, by 8–10%. Since 1952, the glacier area in different regions of the Altai has decreased by 9–27%, and volume by 12–24%. By 2008, as a result of degradation, the total number of glaciers was 953 with an area of 724 km² and volume of 38 km³.     

Enantioselective toxicokinetics study of the bioaccumulation and elimination of α-hexachlorocyclohexane in loaches (Misgurnus anguillicaudatus) and its environmental implications

The enantioselective bioaccumulation and elimination of α-hexachlorocyclohexane (α-HCH) in loaches (Misgurnus anguillicaudatus) were studied for the first time. Valid chiral residue analysis methods for α-HCH enantiomers in water and loach samples were established using gas chromatography coupled with electron capture detector and a BGB-172 chiral column. A rapid accumulation process was found during the 39-d bioaccumulation experiment. The α-HCH in loaches reached its maximum on the fourth day, after which it fluctuated slightly, reflecting a balance between elimination and reuptake. The maximum bioaccumulation factor was 728 at the 10 μg L^?1 exposure level. The enantiomeric fraction (EF) values showed that the bioaccumulation was enantioselective with enantioenrichment of (+)-α-HCH in the loaches. The elimination experiment indicated that the degradation kinetics of α-HCH fitted a typical first-order kinetics model, and the half-life was about 5 d. Significant enantioselectivity was observed during the elimination process, with the EFs declining from higher than 0.5–0.39, suggesting (+)-α-HCH is preferentially biotransformed than (?)-α-HCH in loaches. The results reveal a high capacity for α-HCH bioconcentration by loaches and that biotransformation is the main route of decontamination.     

Acute and Chronic Toxicity of Chlorine Dioxide (ClO2) and Chlorite (ClO2ˉ) to Rainbow Trout (Oncorhynchus mykiss) (4 pp)

Goal, Scope and Background Chlorite (ClO2ˉ) is a primary decomposition product when chlorine dioxide (ClO2) is added during water treatment; therefore the toxic effects of both compounds on aquatic organisms are possible. Limited data are available concerning their toxicity to fish. The aim of this study was to investigate sensitivity of rainbow trout to acute and chronic toxicity of chlorine dioxide and chlorite, and to estimate the Maximum-Acceptable-Toxicant-Concentration (MATC) of those compounds in fish. Methods The acute and chronic toxicity of chlorine dioxide and chlorite to larval and adult rainbow trout was investigated in 96-hour to 20-day laboratory exposures evaluating the wide range spectrum of biological indices under semi-static conditions. Results and Discussion Median lethal concentration (96-hour LC50) values derived from the tests were: 2.2 mg/l for larvae; 8.3 mg/l for adult fish and 20-day LC50 for larvae was 1.6 mg/l of chlorine dioxide, respectively. Chlorite was found to be from 48 to 18 times less acutely toxic to larvae and adult fish, correspondingly. Both chemical compounds induced similar toxic effects in rainbow trout larvae during chronic tests (they affected cardio-respiratory and growth parameters), but chlorine dioxide had a higher toxic potency than chlorite. A significant decrease in the heart rate and respiration frequency of larvae was established. However, within an increase in exposure duration recovery of cardio-respiratory responses was seen to have occurred in larvae exposed to chlorite. Meanwhile, in larvae exposed to chlorine dioxide, a significant decrease in cardio-respiratory responses remained during all 20-day chronic bioassays. Chlorine dioxide also more strongly affected growth parameters of rainbow trout larvae at much lower test concentrations. Decreased rate of yolk-sack resorption occurred only in the tests with chlorine dioxide. Conclusions Maximum-Acceptable-Toxicant-Concentration (MATC) of 0.21 mg/l for chlorine dioxide and of 3.3 mg/l for chlorite to fish was derived from chronic tests based on the most sensitive parameter of rainbow trout larvae (growth rate). According to substance toxicity classification accepted for Lithuanian inland waters, chlorine dioxide and chlorite can be referred to substances of \moderate\ toxicity to fish. Recommendations and Outlook Due to its very reactive nature, chlorine dioxide is rapidly (in a few hours) reduced to chlorite, which is persistent also as a biocide but 16 times less toxic to fish, according to MATC. Therefore, it is much more likely that fish will be exposed to chlorite than to chlorine dioxide in natural waters. Presently accepted, the Maximum-Permitted-Concentration of total residual chlorine (TRC) in waste-water discharging into receiving waters is 0.6 mg/l. If this requirement will not be exceeded, it is unlikely that fish would be exposed to lethal or even to sublethal concentrations of chlorine dioxide or chlorite. Furthermore, chlorine dioxide does not generate toxic nitrogenous (chloramines) or carcinogenic organic residuals (trihalomethanes). All these properties make chlorine dioxide a more promising biocide than chlorine.     

Partitioning of formaldehyde between air and ice at −35°C to −5°C

The equilibrium partitioning of formaldehyde (HCHO) between air and snow was studied in a series of laboratory experiments conducted at −5°C, −15°C, and −35°C, in order to understand how partitioning of HCHO between air and polar snow varies with temperature, and thus seasonally on the ice sheet. Measured partitioning coefficients were 56, 93, and 245 mol l⁻¹ atm⁻¹ for −5°C, −15°C and −35°C, respectively, showing a similar trend as the values previously estimated from field observations. Estimates of the pseudo-first-order rate coefficient for air–snow exchange for the same three temperatures were 4.1×10⁻⁴, 1.1×10⁻⁴, and 1.1×10⁻⁵ s⁻¹, respectively. This implies a time scale for air–snow equilibration of the order of hours to days for HCHO accumulated at or near the ice–air interface on snow grains. Comparing the current laboratory partitioning coefficients with those estimated from measurements of air and freshly fallen snow in Greenland during summer demonstrates that the snow is supersaturated and should degas HCHO to the surrounding air. During this degassing, polar snow should be a significant source of HCHO to the lower troposphere.     

Selected trace metals in oysters (Crassostrea iridescens) and sediments from the discharge zone of the submarine sewage outfall in Mazatlán Bay (southeast Gulf of California): chemical fractions and bioaccumulation factors

Concentrations of Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn in the soft tissue of Crassostrea iridescens and the associated surface sediments (bulk and bioavailable metal concentrations) from an area influenced by a sewage outfall in Mazatlán Bay (southeast Gulf of California), were determined by atomic absorption spectrophotometry. Significant spatial differences in metal concentrations in both the bulk and bioavailable forms in the sediments were identified. An enrichment of Cu, Ni, Pb and Zn in sites located on a south-north transect was detected indicating a dominant influence of the sewage outfall toward the north. C. iridescens accumulated more Zn, Cu, Ni, Fe, Cd; and less Mn, Cr and Pb than were bioavailable in the sediments, as measured using conventional extraction analysis. The degree of enrichment and the bioavailable metal concentrations in the sediments of the south portion of Mazatlán Bay is discussed. The potential ability of C. iridescens as a biomonitor of metallic pollutants is postulated.     

Occurrence of organochlorine pesticides (OCPs) and their enantiomeric signatures, and concentrations of polybrominated diphenyl ethers (PBDEs) in the Adélie penguin food web, Antarctica

Concentrations and enantiomeric signatures of organochlorine pesticides were determined in Antarctic krill, emerald rockcod and Adélie penguin from the Ross Sea, Antarctica. HCB and DDTs were prevalent contaminants in penguin eggs. The highest concentrations of SigmaHCHs (1.35 +/- 0.72 ng/g) were found in the rockcod muscle, where gamma-HCH (1.23 +/- 0.67 ng/g) was the principal isomer. The ratio gamma-HCH/alpha-HCH was evaluated. Enantioselective gas chromatography was used for the evaluation of enantiomeric fractions (EFs) for alpha-HCH and oxychlordane. An increase of 14% in the (+)alpha-HCH enantiomer was found from krill through penguin, suggesting the enantioselective biotransformation increased proportionately with trophic level. Polybrominated diphenyl ethers (PBDEs) were measured and their concentrations were 5.6 +/- 1.12, 5.81 +/- 2.32, 4.57 +/- 0.17 and 3.06 +/- 3.27 ng/g lipids in krill, rockcod muscle, rockcod homogenate and penguin eggs, respectively. The detection of BDE28, BDE47, BDE99 and BDE100 in Antarctic organisms confirmed their global transport and distribution; the detection of lower brominated congeners suggested a potential long-range transport.     

Experimental study on the survival of the water hyacinth (Eichhornia crassipes (Mart.) Solms—Pontederiaceae) under different oil doses and times of exposure

In the last decades, petroleum activities have increased in the Brazilian Amazon where there is oil exploration on the Urucu River, a tributary of the Amazon River, about 600 km from the city of Manaus. Particularly, transportation via the Amazon River to reach the oil refinery in Manaus may compromise the integrity of the large floodplains that flank hundreds of kilometers of this major river. In the Amazon floodplains, plant growth and nutrient cycling are related to the flood pulse. When oil spills occur, floating oil on the water surface is dispersed through wind and wave action in the littoral region, thus affecting the vegetation of terrestrial and aquatic environments. If pollutants enter the system, they are absorbed by plants and distributed in the food chain via plant consumption, mortality, and decomposition. The effect of oil on the growth and survival of vegetation in these environments is virtually unknown. The water hyacinth [Eichhornia crassipes (Mart.) Solms] has a pantropical distribution but is native to the Amazon, often growing in high-density populations in the floodplains where it plays an important role as shelter and food source for aquatic and terrestrial biota. The species is well known for its high capacity to absorb and tolerate high levels of heavy metal ions. To study the survival and response of water hyacinth under six different oil doses, ranging from 0 to 150 ml l^?1, and five exposure times (1, 5, 10, 15, and 20 days), young individuals distributed in a completely randomized design experiment composed of vessels with a single individual each were followed over a 50-day period (30-day acclimatization, 20 days under oil treatments). Growth parameters, biomass, visual changes in the plants, and pH were recorded at 1, 5, 10, 15, and 20 days. Increasing the time of oil exposure caused a decrease in biomass, ratio of live/dead biomass and length of leaves, and an increase in the number of dead leaves. Dose of oil and time of exposure are the most important factors controlling the effects of petroleum hydrocarbons on E. crassipes. Although the species is able to survive exposure to a moderate dose of oil, below 75 ml l^?1 for only 5 days, severe alterations in plant growth and high mortality were observed. Therefore, we conclude that Urucu oil heavily affects E. crassipes despite its known resistance to many pollutants.