Methane in ocean waters: Concentration and carbon isotope variability at East Pacific Rise and in the Arabian Sea

Methane concentrations and stable carbon isotope ratios of water samples from the East Pacific Rise (EPR) at 21°S and the Arabian Sea (24°N, 65°E) have been determined. EPR surface water is in equilibrium (ca. 50 nl/L and –50<¹³CH₄<–46) with atmospheric methane. Deep background water has the signature of the remaining fraction of atmospheric methane partially oxidized in the water column by bacteria. Bottom near, hydrothermally influenced vent methane (>100nl/L and –30<¹³CH₄<–22) is detectable only close to the seep site. There is no input of hydrothermal methane into the atmosphere. EPR water is considered to be rather a sink than a source of atmospheric methane. Surface waters of the Arabian Sea are enriched in methane relative to the atmosphere (source for atmospheric methane). Carbon isotope ratios point to a bacterial origin of methane (¹³CH₄<–55) that is generated in the surface waters. Concentration changes and variations of carbon isotope ratios also suggest that methane seeping from the sea floor sediments of the Arabian Sea is oxidized by bacterial activity and does not reach the atmosphere.     

The effects of salinity,temperature and sediment on the toxicity of copper to juvenile Hediste (Nereis) diversicolor (O. F. Muller)

Without sediment, increasing salinity (7.3 to 29.2) and increasing temperature (12 to 22 °C) reduced the toxicity of copper to juvenile Hediste diversicolor. The LC₅₀ values ranged from 357 gL^-1 in 7.3 to 513 g L^-1 in 29.2 at 12°C and from 247 to 500 g L^-1 at 22°C. In deionized water all the juvenile were dead in all solutions to which copper was added (100 to 600 g L^-1). Dead worms were swollen and everted their pharynxs. In higher doses of copper (500 to 600 g L^-1) the worms were abnormal in behaviour in all salinities (0 to 29.2). The ability to swim or crawl was disturbed.With sediments increasing temperature and increasing salinity increased the toxicity of copper to the worms. The LC₅₀ values ranged from 3200 to 4100 g L^-1 at 22°C. The response of the juvenile to copper was antagonistic to increasing temperature and salinity and synergistic to increasing salinity and increasing temperature without and with the sediment respectively.     

Routine Measurement of Dissolved Inorganic 15N in Precipitation and Streamwater

The difficulty of measuring 15N in dilute solutions has limited the potential of ecosystem labeling experiments and model comparisons. By concentrating the N from large (up to 20 L) water samples on ion-exchange resin columns, we obtained enough N for accurate and reproducible 15N measurement using the Teflon tape diffusion method. Analysis of standards demonstrated >95% recovery of inorganic N from samples, and 15N values comparable to those obtained using standard distillation methods. The value of the blank at our laboratory was 0.16 moles N. Analytical precision was within 2 15N when samples of streamwater from the Bear Brook Watersheds (1800 eq · ha-1 · yr-1 N addition at 192 15N) were kept frozen until analysis. The analytical process is lengthy, but once set up can easily be performed for large numbers of samples.     

Using Mussel Isotope Ratios to Assess Anthropogenic Nitrogen Inputs to Freshwater Ecosystems

Stable nitrogen isotope ratios (¹⁵N) of freshwater mussels from a series of lakes and ponds wererelated to watershed land use characteristics to assess their utility in determining the source ofnitrogen inputs to inland water bodies. Nitrogen isotope ratiosmeasured in freshwater musselsfrom 19 lakes and ponds in Rhode Island, U.S.A., ranged from4.9–12.6 and were found tosignificantly correlate with the fraction of residential development in 100 and 200 m bufferzones around the ponds. Mussel ¹⁵N values in 12 of the 19 ponds also showed significantcorrelation with average dissolved nitrate concentrations, which ranged from 23–327 g L^-1.These observations, in light of previous studies which link elevated¹⁵N values of nitrogenderived from septic wastewater with those seen in biota, suggest that mussel isotope ratios mayreflect nitrogen source in freshwater ecosystems. We followed aniterative approach usingmultiple regression analysis to assess the relationship between mussel¹⁵N and the land usecategories fraction residential development, fraction feedlotagriculture, fraction row-cropagriculture, and fraction natural vegetation in 100 and 200 m bufferzones and pond watersheds.From this we developed a simple regression model to predict mussel¹⁵N from the fraction ofresidential development in the 200 m buffer zone around the pond.Subsequent testing with datafrom 16 additional sites in the same ecoregion led us to refine themodel by incorporating thefraction of natural vegetation. The overall average absolute differencebetween measured andpredicted ¹⁵N values using the two-parameter model was 1.6. Potential sources of error inthe model include differences in the scale and categorization ofland-use data used to generate andtest the model, differences in physical characteristics, such asretention time and range ofresidential development, and exclusion of sources of enrichednitrogen such as runoff from feedlot operations or increased nitrogen loading from inefficient or failed septic systems.     

The effect of temperature and salinity on copper body-burden and copper toxicity to Hediste (Nereis) diversicolor

Temperature from 12 to 22°C and salinity from 30.5 to 7.6 increased accumulation of copper in Hediste diversicolor. Copper accumulated ranged from 85.83 to 217.14 g g^-1. Sediments reduced accumulation of copper under temperature-salinity combinations. Accumulated copper ranged from 90.19 to 153.26 g g^-1.However, mortality of the worms was not solely dependent upon copper body-burden. It ranged from 34 to 45% and from 38 to 80% in the presence of sediment. A combination of osmoregulatory and thermal stresses increased the toxic effect of copper to the worms.     

A Survey of Trace Metals in Vegetation, Soil and Lower Animal Along Some Selected Major Roads in Metropolitan City of Lagos

The concentration of trace metals (Cd, Cu, Pb and Zn) in a total of 144 samples of grass, soil and lower animal (earthworm, Lybrodrilus violaceous) were collected and analysed for their metallic content. Levels of cadmium ranged from 0.01–0.07 g g^–1; 0.01–0.12 g g^–1 and from trace–0.05 g g^–1 dry weight for plant, soil and animal samples respectively. Mean concentration of copper ranged 0.10–1.48 g g^–1; 0.10–2.90 g g^–1 and 0.01–0.08 g g^–1 for samples in similar order as above. The levels of Pb varied from 0.01–0.14 g g^–1; 0.02–0.23 g g^–1 and from trace–0.07 g g^–1 while that of Zn ranged from 0.19–1.80 g g^–1; 0.51–3.35 g g^–1and 0.01–0.08 g g^–1 also in the same order of samples as mentioned above. Levels of metals in soil samples were higher than the background levels with the exception of Zn but lower than European Union (EU) limits. The results generally revealed the presence of metals in plant and animal samples and metal dynamics up the food chain is highly possible. Acceptable recoveries of the spiking experiment validate the experimental protocol.     

Monitoring of the atmospheric burdens of CH4, N2O,CO, CHCIF2 and CF2Cl2 above Central Europe during the last decade

Based on high spectral resolution infrared solar observations made at the International Scientific Station of the Jungfraujoch, Switzerland, total vertical column abundances of 18 atmospheric gases have been monitored routinely since 1984. The observed temporal evolutions in the columns of CH₄, N₂O, CO, CHClF₂ (HCFC-22) and CF₂Cl₂ (CFC-12) are reported here as typical examples of this monitoring effort which is conducted within the frame of Global Change and Network for the Detection of Stratospheric Change programs.     

The effect of salinity,temperature and time on the accumulation and depuration of copper in ragworm,Hediste (Nereis) diversicolor (O.F. Muller)

Under a low temperature condition of 12°C, accumulation of copper by the ragworm, Hediste (Nereis) diversicolor, increased at low salinity of 7.6 but was reduced at intermediate and high salinities of 15.25 and 30.5, respectively. Copper contents of the worms at low salinity and temperature ranged from 68 to 185 µg/g. Under increasing temperature of 17 and 22°C, bioavailability of copper to the worms increased irrespective of salinity gradient. The copper contents of the worm ranged from 59 to 784 µg/g dry weight. ANOVA analysis of data showed that salinity did not significantly affect accumulation of copper by the worm. Temperature significantly affected accumulation. The interaction of salinity and temperature was significant and complex, and days of exposure did not influence accumulation. Depuration of copper by the worm was independent of salinity which ranged from 510 to 15.6 µg/g. Temperature significantly affected depuration. The interaction of salinity and temperature was significant. However, individual worms neither accumulated nor depurated at the same rate.     

Trihalomethane Formation Potential and Concentration Changes During Water Treatment at Mumbai (India)

The treated water at the outlet oftreatment plants and representative servicereservoirs of Mumbai city have been evaluatedfor trihalomethane formation potential in1995–1996. Chloroform, dichlorobromomethane,chlorodibromomethane and bromoform have beenmonitored during monsoon, winter and summer.The levels of chloroform are found above theregulated WHO guideline value of 200 g L^-1 in final water during postmonsoon atGhatkopar (226 g L^-1), Malbar (210.3 g L^-1) and Tulsi (231.26 g L^-1).     

Respiratory Suspended Particulate (RSP) Concentration and its Implications to Roadside Workers: A Case Study of Hong Kong

The adsorption behaviour of Diphenylamine (DPAM), napthylamine ( NAM), napthylamine ( NAM)and aniline on pyrolusite and activated carbon has been studied.Pyrolusite shows remarkable sorption capacity for DPAM and NAM as compared to aniline; (the adsorption followed theorder:Activated Carbon: DPAM = NAM > AnilinePyrolusite: DPAM: NAM > NAM> Aniline)The maximum adsorption of NAM occurred in theconcentration range 4–20 g mL^-1 on pyrolusite (95%)and 4–50 g mL^-1 on activated carbon (100%). Theeffect of various doses of activated carbon on the adsorption of NAM confirm Langmuir and Freundlich isotherms where asFreundlich isotherm is obeyed by pyrolusite. The adsorption of NAM on both the absorbents is not affected in presence ofDPAM over a wide range of their initial concentrations (20–60g mL^-1). The desorption studies of NAM onpyrolusite was carried out by batch as well as column processes.Excellent results were obtained when a mixture of n-hexane andisopropanol (91:1) was used as eluent.     

Characterization of atmospheric dust at Gurushikar,Mt. Abu,Rajasthan

The nature of atmospheric aerosols at Gurushikar, Mt. Abu, Rajasthan where a gamma ray telescope is to be installed, was investigated. Air particulate samples collected on filters were used to estimate the total suspended particulate matter (TSPM) and its elemental composition. The TSPM varied from 31 to 103 g/m³ during January to March 1994. The heighest loads were observed during the months of May and June (80–100 g/m³) and lowest during October (20–60 g/m³). The dust was also examined for size, shape and nature of the mineral matter. The particle sizes varied from 100 m to 5 m. The course particles (>50 m) are irregular shaped quartz grains. Some of the medium size (=50 m) particles were spherical and were highly conducting. These particles were rich in iron content. Correlation coefficients among various elements in the dust showed that it is made up of mainly two components-wind blown ground dust and particulate arising out of wood and coal burning.     

Environmental Contaminants in Blood, Hair, and Tissues of Ocelots from the Lower Rio Grande Valley, Texas, 1986–1997

The ocelot (Felis pardalis) isan endangered neotropical cat distributed within asmall range in the Lower Rio Grande Valley (LRGV), inTexas, U.S.A. Studies of the impacts of environmentalcontaminants in wild cats are few. Approximately onefourth of the estimated population (about 100) ofocelots in the LRGV was sampled to evaluate theimpacts of chlorinated pesticides, polychlorinatedbiphenyls, and trace elements on the population. Hairwas collected from 32 ocelots trapped between 1986–1992,and blood was collected from 20 ocelots trappedbetween 1993–1997. A few blood samples were obtainedfrom individuals recaptured two or three times. Tissue samples from 4 road-killed ocelots were alsoanalyzed. DDE, PCBs, and Hg were some of the mostcommon contaminants detected in hair and blood. MeanHg levels in hair ranged from 0.5 to 1.25 g g^-1 dw,Se from 1.5 to 3.48 g g^-1 dw, and Pb from 0.56 to26.8 g g^-1 dw. Mean DDE concentrations in plasma ranged from 0.005 g g^-1 ww to 0.153 g g^-1 ww, and PCBs ranged from 0.006 g g^-1 ww to 0.092 g g^-1 ww. Mean Hg levels in red blood cells rangedfrom 0.056 g g^-1 dw to 0.25 g g^-1 dw. Concentrations of DDE, PCBs, or Hg, did not increasesignificantly with age, although the highestconcentrations of DDE and Hg were found in olderanimals. Overall, concentrations of DDE, PCBs, and Hgwere low and at levels that currently do not pose anythreat to health or survival of the ocelot. This isfurther supported by good reproduction of the ocelotin the LRGV, where adult females averaged about 1.5kittens/litter. Thus, it seems that the current majorthreat to recovery of the ocelot in the LRGV may behabitat loss, although potential impacts of newgeneration pesticides, such as organophosphorus andcarbamate insecticides need further study.     

Roadside Concentration of Gaseous and Particulate Matter Pollutants and Risk Assessment in Dar-Es-Salaam, Tanzania

This study used manual air sampling method to assess the contribution of road traffic to air pollution level in Dar-es-Salaam City, Tanzania. Samples were collected from 11 different sites. Parameters measured were: sulphur dioxide using pararosaniline method, nitrogen dioxide using saltzman method, particulate matter and particulate lead using filtration method and atomic absorption spectrometric method, respectively. Results showed that hourly average sulphur dioxide concentration range from 127 to 1385 g/m³. The measured values of sulphur dioxide were above the recommended WHO guidelines with an hourly objective value of 350 g/m³ at 87% of the sampling sites. The hourly average nitrogen dioxide concentration ranged from 18 to 53 g/m³. The maximum hourly nitrogen dioxide concentration at 53 g/m³ was below the WHO guideline value of 200 g/m³. The hourly average suspended particulate matter (SPM) ranged from 98 to 1161 g/m³, exceeding the recommended value of 230 g/m³ by WHO at 87% of the sampling sites. The hourly average lead concentration was found to range from 0.60 to 25.6 g/m³, exceeding again the WHO guideline value of 1.5 g/m³at 83% of the sampling sites. Results predicted by Gaussian model when compared with the measured values were found to have a correlation coefficient of 0.8, signifying a good correlation. The risk assessment was undertaken considering the people who spend a significant portion of their time near the roads, such as the Uhuru primary school pupils and the adult population who reside by the roadside. The unit risk realised was 18.2 × 10^–6 for adult population and 2.2 × 10^–6 for pupils, both scenarios showing risk higher than the United Sates of America Environmental Protection Agency (USEPA) acceptable limit of 1× 10^–6. Considering the magnitude of the problem at hand, this study recommends an introduction of mandatory emission tests of SPM, lead and sulphur dioxide (SO₂). The study further recommends the introduction of continuous and/or regular air quality monitoring and the use non-leaded petrol in Tanzania.     

Concentration and Distribution of Persistent Organic Pollutants (POPs) in Harbour Dredging Sediments: A Pilot Study Using a Statistical Approach for a More Efficient Characterisation and Management

The Italian guidelines concerning the dumping of dredgingmaterials implies chemical, physical and microbiologicalcharacterisation of dumping sediments collected through aspecific sampling strategy.POP's such as PCB's and organochlorine pesticides, areconsidered as priority pollutants in all the InternationalConventions for the protection of the marine environment, inconsequence of their persistence, toxicity and bioaccumulation capacity.In the present article the concentrations and distribution ofPCB's and organochlorine pesticides in dredging sediments ofPiombino harbour (northern Thyrrenian sea) were investigates.The results showed high POP's concentrations in all the studiedareas. The maximum values were: 3.94 mg kg^-1 dry weight for PCB's(IUPAC Nos. 28; 52; 101, 118; 137; 153; 180; 209); 2.04 mg kg^-1 d.w.for HCH's (-, -, - and -hexachlorocyclohexane isomers); 0.28 mg kg^-1 d.w. for DD's (DDT + DDE + DDD).Subsequently, the data related to each pollutant were treatedwith statistical tests, in order to verify how well the samplingstrategy is able to represent the distribution of contaminantsin the dredging area. Finally, management strategies werederived for the studied dredging sediments.     

Monitoring the results of Canada/U.S.A acid rain control programs: some lake responses

Aquatic acidification by deposition of airborne pollutants emerged as an environmental issue in southeastern Canada during the 1970s. Drawing information from the extensive research and monitoring programs, a sequence of issue assessments demonstrated the necessity of reducing the anthropogenic emissions of acidifying pollutants, particularly sulphur dioxide (SO₂). The 1991 Canada-U.S. Air Quality Agreement (AQA) was negotiated to reduce North American SO₂ emissions by 40% relative to 1980 levels by 2010, and at present, both countries have reduced emissions beyond their AQA commitment. In response to reduced SO₂ emissions, atmospheric deposition of sulphate (SO₄ ^2–) and SO₄ ^2– concentrations in many lakes have declined, particularly in south-central Ontario and southern Québec. Sulphate deposition still exceeds aquatic critical loads throughout southeastern Canada however. Increasing pH or alkalinity (commonly deemed recovery) has been observed in only some lakes. Several biogeochemical factors have intervened to modify the lake chemistry response to reduced SO₄ ^2– input, notably release of stored SO₄ ^2– from wetlands following periods of drought and reduction in the export of base cations from terrestrial soils. Three examples from Ontario are presented to illustrate these responses. Significant increases in pH and alkalinity have been observed in many lakes in the Sudbury area of Ontario due to the large reductions in local SO₂ emissions; early-stage biological recovery is evident in these lakes. An integrated assessment model predicts that AQA emission reductions will not be sufficient to promote widespread chemical or biological recovery of Canadian lakes. Monitoring and modeling are mutually supporting assessment activities and both must continue.     

Performances and application of a passive sampling method for the simultaneous determination of nitrogen dioxide and sulfur dioxide in ambient air

The performances and applicability of a diffusion tubesampler for the simultaneous measurements of NO₂ andSO₂ in ambient air were evaluated. SO₂ andNO₂are collected by the passive sampler using triethanolamine astrapping agent and are determined as sulphate and nitrite withion chromatography. The detection limit (2.3 g m^-3 ofNO₂ and 4.2 g m^-3 of SO₂ for two weekssampling) is adequate for the determination of concentrationsin urban and industrial areas. Precision of the method as RSDis in mean 5% for NO₂ and 12% for SO₂ at theconcentration levels in urban areas. Calibration of the methodwas performed in the field conditions by comparison between theresponses of sampler and the concentrations measured by thecontinuous monitors. High degree of linearity (correlationcoefficients > 0.8) is found between the passive sampler tubeand the continuous monitor data for both NO₂ and SO₂.To reduce the wind velocity influence on passive sampling ofdiffusion tubes, a protective shelter was tested in this study.The overall uncertainty of one measure for the optimised methodis estimated at 5 g m^-3 for NO₂ and 6g m^-3 for SO₂. Suitability of this passivesampling method for air pollution monitoring in urban areas wasdemonstrated by the results shown in this paper on a campaigncarried out in the French agglomeration.     

Excised Barley root uptake of several 14C labeled organic compounds

Many organic pollutants potentially are available for uptake by plants and thus bioaccumulation and food contamination. One method of studying uptake is with excised roots, a technique extensively used with plant nutrients. A similar method was developed and used to evaluate uptake patterns of several ¹⁴C-labeled organic chemicals. Uptake rate constants for the chemicals tested occurred in the following order: captan phenol > aniline > ethanol indole trifluralin propanil > 1,2,4-trichlorobenzene (TCB) > nitrobenzene atrazine > bromacil > simazine > monuron.     

SMOKE CONCENTRATION AS AN INDICATOR OF POLYCYCLIC AROMATIC HYDROCARBONS LEVELS IN THE AIR

The relationship of polycyclic aromatichydrocarbons (PAH) and smoke concentrationwas analysed at four different locations in Zagreb during theheating season. At two sampling sitessmoke pollution came primarily from domestic heating while theother two sites were under a directinfluence of traffic. At locations away from trafficcorrelations between smoke and PAH concentrationswere stochastically significant at 0.01 level. Takingbenzo-a-pyrene (BaP) as a PAH representative itwas shown that for these two locations the smoke/BaPrelationship can be presented with a singleregression line which can serve for rough assessment of BaPlevels in the air. The BaP concentrationof 10 ng/m³ – proposed by the German FederalEnvironmental Agency as orientation < mark (Lahman et al., 1984) – might be expected to occurat smoke levels 60 g/m³,and above this level it is recommended to start measuringactual concentrations of PAH.     

Simultaneous determination of parathion and p-nitrophenol in vegetable tissues by derivative spectrophotometry

A first derivative spectrophotometric method has been developedfor the determination of parathion and p-nitrophenol in vegetabletissues. Ethanol was used as solvent for extracting the compoundsfrom the tissues and subsequently the samples were evaluated against a vegetable tissue blank, directly by derivative spectrophotometry. The simultaneous determination of these compounds can be carried out using the zero-crossing approach for parathion at 253.0 nm and for p-nitrophenol at 273.1 nm. In the samples each analyte was determined in the presence of one another in the ranges between 4.9 to 3883.5 g g^-1 forparathion and 4.9 to 3285.3 g g^-1 for p-nitrophenol.The detection limits (3) were found to be 1.5 and 1.4 g g^-1 for parathion and p-nitrophenol, respectively. The relative standard deviations were in all instances less than1.8%. The proposed method was applied to the determination ofthe analytes in spiked leafs of corn. The results show a goodrecovery and they are in agreement with those obtained bypolarography.     

Aldehyde Concentrations in Ambient Air of Coastal Georgia, U.S.A.

Aldehydes are an airborne byproduct of many industrialprocesses, vehicle transportation, and emissions fromnumerous natural sources. To characterize aldehydeconcentrations in ambient air of the Savannah, Georgiaarea, air samples for 3 aldehydes (formaldehyde,acetaldehyde, and propionaldehyde) were collected atfive sites on a monthly basis over a 12-month periodfrom December of 1995 through November 1996. Four ofthe sites were in central Savannah and the fifth sitewas located in a rural area about 56 km south ofSavannah. During each 24-hr sampling episode, sampleswere collected in two 12-hr periods approximatingdaylight and nighttime hours, following U.S. EPAMethod TO-11. Formaldehyde concentrations ranged from0.17 to 6.80 g m^-3, acetaldehydeconcentrations ranged from 0.07 to7.60 g m^-3, and propionaldehyde levels rangedfrom 0.02 to 9.10 g m^-3. On average, thefour sites in Savannah had higher aldehydeconcentrations than the rural site (2.0 versus1.2 g m^-3 for formaldehyde, 2.3 versus1.7 g m^-3 for acetaldehyde, and 1.2 versus1.0 g m^-3 for propionaldehyde). The daytimeconcentrations for formaldehyde and acetaldehyde werehigher than the nighttime levels. The data from allthe sites were within published worldwide backgroundvalues for aldehydes.