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).     

The Bear Brook Watershed, Maine (BBWM), USA

The Bear Brook Watershed Manipulation project in Maine is a paired calibrated watershed study funded by the U. S. EPA. The research program is evaluating whole ecosystem response to elevated inputs of acidifying chemicals. The project consists of a 2.5 year calibration period (1987-1989), nine years of chemical additions of (NH4)2SO4 (15N- and 34S-enriched for several years) to West Bear watershed (1989-1998), followed by a recovery period. The other watershed, East Bear, serves as a reference. Dosing is in six equal treatments/yr of 1800 eq SO4 and NH4/ha/yr, a 200% increase over 1988 loading (wet plus dry) for SO4 and 300% for N (wet NO3 + NH4). The experimental and reference watersheds are forested with mixed hard- and softwoods, and have thin acidic soils, areas of 10.2 and 10.7 ha, and relief of 210 m. Thin till of variable composition is underlain by metasedimentary pelitic rocks and calc-silicate gneiss intruded by granite dikes and sills. For the period 1987-1995, precipitation averaged 1.4 m/yr, had a mean pH of 4.5, with SO4, NO3, and NH4 concentrations of 26, 14, and 7 eq/L, respectively. The nearly perrenial streams draining each watershed have discharges ranging from 0 (East Bear stops flowing for one to two months per year) to 150 L/sec. Prior to manipulation, East Bear and West Bear had a volume weighted annual mean pH of approximately 5.4, alkalinity = 0 to 4 eq/L, total base cations = 184 eq/L (sea-salt corrected = 118 eq/L), and SO4 = 100 to 111 eq/L. Nitrate ranged from 0 to 30 eq/L with an annual mean of 6 to 25 eq/L; dissolved organic carbon (DOC) ranged from 1 to 7 mg/L but was typically less than 3. Episodic acidification occurred at high discharge and was caused by dilution of cations, slightly increased DOC, significantly higher NO3, and the sea-salt effect. Depressions in pH were accompanied by increases in inorganic Al. The West Bear catchment responded to the chemical additions with increased export of base cations, Al, SO4, NO3, and decreased pH, ANC, and DOC. Silica remained relatively constant. Neutralization of the acidifying chemicals occurred dominantly by cation desorption and mobilization of Al.     

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.     

Insecticide Contamination of Jamaican Environment. V. Island-Wide Rapid Survey of Residues in Surface and Ground Water

Residues of organochlorines and organophosphates were determined by gas chromatography in water and sediment from 26 locations in 17 major rivers, 7 natural springs and 13 wells across Jamaica. Samples were collected on only one occasion between May and July, 1994. Residues of endosulfan were detected in all but three rivers; -endosulfan in 15 samples of sediment (0.9–108.1, mean = 28.93, S.E. = 7.198 g kg-1) and 13 of water (0.01–0.35, mean = 0.11, S.E. = 0.035 g L-1), -endosulfan in 5 sediment (15.29–49.35, mean = 30.56, S.E. = 7.132 g kg-1) and 12 water (0.05–0.31, mean = 0.14, S.E. = 0.031 g L-1) samples, and endosulfan sulphate in waters of three rivers (0.003–0.244 g L-1). Chlorpyrifos was present in 9 sediment (0.423-135.2, mean = 18.38, S.E. = 10.699 g kg-1) and two water (0.001–0.022 g L-1) samples, diazinon and ethoprophos in the sediment of one river each. Mean levels (g L-1) of and isomers and sulphate of endosulfan were 0.16 (S.E. = 0.057), 0.12 (S.E. = 0.036) and 0.15 (S.E. = 0.089), respectively, in four of the seven springs and 0.23 (S.E. = 0.052), 0.11 (S.E. = 0.029) and 0.26 (S.E. = 0.088), respectively, in seven of the thirteen wells monitored.     

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.     

The monitoring of cadmium,zinc and copper in the kidneys and liver of humans deceased in the region of Cracow (Poland)

Cadmium, zinc and copper levels were determined in the renal cortex and liver of 60 inhabitants of Cracow, Poland. Cadmium levels in the renal cortex were contained in broad limits of 5–176 g/g, mean 50.6 g/g (wet weight). Maximum levels were found in the age group of about 50–60 years. The levels were slightly higher in men (53 g/g) than in women (45 g/g), with no effect of location within the region. The levels in smokers (62 g/g) were much higher than in non-smokers (32 g/g). The above relations were less pronounced for cadmium levels in the liver. Whole body retention of cadmium followed the pattern of cadmium in renal cortex. The level of zinc in renal cortex reflected those of cadmium. A significant proportion of the population (54% in smokers, 9% in non-smokers) showed cadmium levels in renal cortex exceeding the reference level of 50 g/g recently accepted for general population. In the view of the authors the exposure to cadmium of the population of Cracow is excessive and calls for attention.The study was performed under a KBN grant No 40106 91 01.     

Atmospheric Dust Loads and Their Elemental Composition at a Background Site in India

Air particulate samples collected during 1995–96 ata background site situated on the east coast of Thar Desert inRajsthan State of India were analysed for atmospheric dustloads (Suspended Particulate Matter) and elemental composition.The values of SPM ranged from 9 g M^-3 to 97g M^-3 with an average of 43 g M^-3 except a fewepisodic values, which were 3 to 5 times higher than the averageduring summer months. The results for elemental composition ofthe particulate samples showed that the concentrations ofanthropogenic toxic trace elements viz. Br, Cr, Pb, Sb, Se and Znare lower by a factor of 2 to 10 as compared to urban areas. Thehigh enrichment factors for anthropogenic elements viz. Br, Pb,Sb and Zn show an input from coal/wood fuel burning andvehicular pollution at the sampling site. The depletion of Si inSPM samples shows long distance transport of dust to the samplingsite.     

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.     

Chemistry of Dissolved Organic Carbon at Bear Brook Watershed, Maine: Stream Water Response to (NH4)2SO4 Additions

This study was conducted to determine the response of stream water DOC and organic acidity to increased inputs of ammonium sulfate to a whole catchment. Precipitation, throughfall, soil solutions (from Spodosols) and stream waters were characterized for DOC concentrations and fractions (hydrophobic acids and neutrals, hydrophilic acids, bases, and neutrals) in both the control (East Bear) and the treatment (West Bear) catchments of Bear Brook Watershed, Maine (BBWM), a northern hardwood forest. In all solutions except precipitation, DOC was composed primarily of organic acids, with hydrophobic acids dominating (> 60% of DOC) in forest floor leachates (5000 mol C L-1), and a balance of hydrophobic and hydrophilic acids in deep B horizons and stream waters ( 150 mol C L-1). Stream waters had higher concentrations of DOC during storm or snowmelt events (high discharge), often reaching 300 to 400 mol C L-1. Forest floor leachate C was rapidly attenuated by the mineral soils under all flow conditions, indicating how important mineral soil sorption of DOC was in reducing the loss of C via surface water from BBWM. No differences occurred between control and treatment streams for concentration or composition of DOC due to treatment from 1989 through 1994. In 1995, West Bear Brook had much lower concentrations of DOC than East Bear for the first time. However, this occurred during a year of record low runoff, suggesting that hydrology may have affected export of C. Average annual export of DOC from the catchments was similar (1000 to 2000 mol C ha-1 yr-1). Organic anions in streamwaters increased slightly during high flow events (e.g., East Bear had means of 15 and 19 eq L-1 organic anions during base flow and high discharge in 1995). Treatment of West Bear caused a decrease in organic anions, both in concentration and contribution to overall anion composition (organic anions during high discharge as a percentage of total anions decreased from about 8 to 4% for 1987-89 and 1993-95 samples, respectively). This was probably due to decreased solution pH (greater protonation of organics) and higher concentrations of inorganic anions. Overall, there were no clear, detectable changes in stream water DOC, with only minor changes in organic anions, as a result of treatment with ammonium sulfate.     

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.     

A Regional Analysis of Lake Acidification Trends for the Northeastern U.S., 1982-1994

Acidic deposition is a regional phenomenon, but its effects have traditionally been studied using site-specific, intensive monitoring. We present trends information for 36 lakes of high-to-moderate acid sensitivity (defined as acid neutralizing capacity [ANC] < 100 eq L-1), and 15 deposition monitoring stations, in the northeastern U.S. for the period 1982-1994. Trends at each site were assessed through use of the Seasonal Kendall tau test; the resulting statistics were combined, through a technique analogous to analysis of variance, to produce quasi-regional estimates of change for key chemical variables. Rates of sulfate deposition declined significantly across all of the northeastern region during this time period, while rates of nitrate and ammonium deposition were unchanged. All lakes exhibited strong decreases in sulfate concentrations in response to declining sulfate deposition, but there was a strong contrast in the response of acid/base status between lakes in New England and lakes in the Adirondacks. As a group, the New England lakes exhibited recovery (ANC = +0.8 eq L-1yr-1, p<0.001), while the Adirondack lakes exhibited either no trend or further acidification (as a group, ANC = -0.5 eq L-1yr-1, p<0.01). This contrast can be attributed to changes in base cation concentrations: New England lakes exhibited base cations declines that were smaller in magnitude than declines in sulfate, producing the observed recovery in ANC; Adirondack lakes showed base cation declines that were very similar to those of sulfate, and no recovery was evident.     

SEASONAL INFLUENCES OF THE ORGANIC POLLUTION MONITORING OF THE NEW CALABAR RIVER, NIGERIA

Monitoring of the New Calabar River water was conductedmonthly for a period of one year to ascertain seasonalinfluences and industrial effluent discharges on the organicpollution status of the river. Dissolved oxygen (DO) levelsranged between 3.4 and 9.1 mg/l and 4.4–9.0 mg/l for therainy and dry seasons respectively. Total dissolved solids(TDS) levels ranged between 6.5 and 4013.9 mg/l for the rainyseason and 4.32–619.5 mg/l for the dry season. The ranges forthe organic pollutant parameters were: biochemical oxygendemand, 0.25–4.20 mg/l and 0.15–4.95 mg/l; COD, 10–1000mg/l and 15–100 mg/l; oil and grease, 0.00001–5000 g/l and0.00001–800 g/l; anionic surfactants, 2.0–30 gMBAS/l and 0.1–2.0 g MBAS/l for the rainy and dryseasons respectively. The ranges for the same parameters forthe industrial effluent were: DO, 2.1–3.9 mg/l and 6.5–10.8mg/l; BCD, 0.35–1.4 mg/l and 2.3–2.7 mg/l; COD, 508 mg/l and20–576 mg/l; oil and grase, 0.07–50 g/l and0.048–25.0 g/l; and anionic surfactants, 4.0–7.3g MBAS/l and 0,2–17.0 g MBAS/l for the rainyand dry seasons respectively. These results indicate thatseasonal changes as well as industrial effluent dischargesinfluenced the organic load of the river.     

Linkages of P and Al Export at High Discharge at the Bear Brook Watershed in Maine

Phosphorus chemistry in streams was evaluated at the paired watershed study at the Bear Brook Watershed, Maine. The West Bear catchment has been treated bimonthly since 1989 with 1,800 eq (NH4)2SO4 ha-1 yr-1. East Bear was the untreated reference watershed. During 1993, concentration of total phosphorus (P) in weekly samples from East and West Bear Brook ranged from 0 to 15 g L-1. The median values were 2 and 4 g L-1 for East and West Bear, respectively. During a high discharge event in January of 1995, the concentration of dissolved P remained relatively constant ( 3 g L-1) as pH decreased from 5.63 to 5.08 and from 5.14 to 4.75 in East and West Bear, respectively. The concentration of total P increased to ca. 60 g L-1 during the rising limb of the hydrograph in West Bear, four times the value in East Bear, total P then declined rapidly as discharge remained high followed by an increase. Dissolved Al increased in both streams during the episodic acidification. West Bear, the more acidic, had concentrations of dissolved Al four times those of East Bear (maximum of 1.1 mg L-1 versus 0.25 mg L-1). Acid-soluble particulate Al increased to 0.2 and 4.2 mg L-1 for East and West Bear, respectively, in parallel to total P (but was 102 greater than total P) and then declined in parallel to total P while discharge remained high. Total P, dissolved P, and particulate Al did not relate to pH. Total P and particulate Al and Fe were strongly correlated. Concurrently, base cations remained relatively constant or decreased slightly. Particulate acid-soluble Al exceeded particulate acid-soluble base cations. We hypothesize that the particulate P was occluded in, or adsorbed on, acid-soluble particulate Al(OH)3. This Al(OH)3. This Al(OH)3 precipitates as emerging acidic groundwater degasses CO2 and pH rises. The export of Al and P is greater from the treated watershed because the induced acidification is translocating more Al from soils to the stream. Most of the export of P is related to acid-soluble Al particulate material.     

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.     

Intake of Chromium by the Adult Population of Mumbai City

Electro Thermal Atomic Absorption Spectrophotometry (ET-AAS), is used for the determination of chromium (Cr) in a variety of environmental matrices. The detection limit for the estimation of Cr is 2 pg absolute for a volume injection of 20 l. The precision of the method is established by analysing Cr from a synthetic mixture containing various elements in different qualities (0.5–10 ppm) and is found to be within ± 8%. The reliability of estimation is further assessed through the analysis of Standard Reference Materials (SRMs) of soil, hay, milk powder and lake sediment obtained from IAEA.The total intake of Cr through air, water and food works out to be 54 g/day for the adult population of Mumbai city. The dietary intake through food is the major contributor to the total intake of Cr. The concentration of Cr in atmospheric air and drinking water collected from different suburbs showed geometric mean concentrations of 0.09 g/m³ and 0.3 g/l, respectively. The daily intake of Cr, though lower, is closer to the lower bound of the recommended value of 50–200 g/day.     

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.     

Distribution of heavy metals in sediment and water of river Gomti

Gomti river receives industrial as well as domestic wastes from various drains of Lucknow city. In the process the water and sediment of the river Gomti get contaminated with heavy metals and other pollutants. In the present study, impacts of domestic/industrial wastes on the water and sediment chemistry of river Gomti with special reference to heavy metals have been investigated in different seasons (summer, winter and rainy). For this, seven sampling sites: Gaughat, Mohan Meakin, Martyrs Memorial, Hanuman Setu, Nishatganj bridge, Pipraghat and Malhaur, in the river Gomti in Lucknow region were identified and samples of water and sediments were collected in all the three seasons. In the collected water and sediment samples, six metals (Cd, Cr, Cu, Ni, Pb, and Zn) were analyzed on ICP-AES (Inductively coupled plasma emission spectroscopy) Labtam Plasmalab 8440. High concentrations of all the metals were noticed in water and sediment in rainy season compared to summer and winter. Because in rainy season runoff from open contaminated sites, agricultural field and industries, directly comes into the river without any treatment. In both the cases, the concentration of zinc was maximum (0.091 g/ml in water and 182.13 g/g in sediment) and the concentration of cadmium (0.001 g/ml in water and 17.26 g/g in sediment) was minimum. Higher concentration of metal in water and sediment during rainy season could be due to the industrial/agricultural/domestic runoff coming into the river.     

The distribution of molybdenum in the tissues of wild ducks

The Mo contents and the relations between Mo and Cu or Crcontents were investigated in the organs of Japanese wild ducks(spotbill duck, pintail, wigeon, scaup and tufted duck). Thehighest Mo content in kidney and liver of the dabbling duckswere more than 30 g g^-1 dry weight (g g^-1 d.wt.), though that of diving ducks were less than 11 gg^-1 d. wt. The contents were lower in the ducks migratingwithin Japan, Eurasia and North America than those in the birdsmigrating between Japan and Eurasia. The contents of liver inall species were more than 50 and less than 5 g g^-1 d.wt. for Cu and Cr, respectively. Significant correlations werefound between Mo and both elements in pintail and scaup, and Moand Cr in tufted duck. These results suggest that thecontamination of wild ducks reflects the reproductive area, andnot the collected area. Mo contents closely correlated with theCu and/or Cr contaminations.     

Concurrent Exposure Assessments of Atrazine and Metolachlor in the Mainstem, Major Tributaries and Small Streams of the Chesapeake Bay Watershed: Indicators of Ecological Risk

The goals of this study were to: (1) measure atrazine and metolachlor concentrations during both high and low use periods in the Chesapeake Bay's mainstem/major tributaries, smaller tributaries and representative small agricultural streams during 1995 and 1996; (2) compare these exposure data with toxicity benchmarks for each herbicide to predict ecological risk and (3) use in-stream fish community data collected in the streams to provide supportive data for ecological risk characterization. Spatially, atrazine (<0.10–98 g/L) and metolachlor (<0.10–68 g/L) concentrations were highest in the streams, followed by the small tributaries (<0.10–11 g/L atrazine; <0.10–8.6 g/L metolachlor) with the lowest concentration in the mainstem Bay/larger tributaries (<0.10–0.22 g/L atrazine; <0.10–0.24 g/L metolachlor). Temporally, concentrations of both herbicides were greatest in all three types of habitats in the late spring and early summer. Concentrations of atrazine and metolachlor were very low or non-detectable in all habitats sampled from early August to mid-April. Toxicity benchmarks of 20 g/L for atrazine based on an ecological No Observed Effect Concentration (NOEC) for microcosm/mesocosm studies and an acute 10th percentile of 53 g/L for metolachlor (protection of ninety % of the species) based on laboratory toxicity data were selected to assess annual and seasonal ecological risk. Both of these toxicity benchmarks were conservative estimates of ecological risk designed to protect the trophic group (plants) most sensitive to these herbicides. Based on a comparison of these toxicity benchmarks with two years of exposure data, the ecological risk from both atrazine and metolachlor exposure in the mainstem Chesapeake Bay/large tributaries, small tributaries and representative agriculturally dominated streams was generally judged to be low. During one 72-h stream rain event in 1995, the atrazine toxicity benchmark (20 g/L) was exceeded during part of the event. However, long-term permanent ecological effects are not expected based on the documented recovery potential of the most sensitive trophic group (plant communities) to the concentrations of atrazine reported and the transient nature of the atrazine pulses. Fish communities at the stream sites receiving the highest concentrations of both herbicides were judged to be healthy based on an Index of Biotic Integrity (IBI) developed for Maryland's coastal plain.     

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.