Viruses on shellfish-growing waters

The conversion of the bivalve shellfish to a virus carriage status is the most important consequence of the virus pollution of shellfish-growing waters. Virus carriage has public health implications of significance for consumers of raw or inadequately cooked shellfish, as well as general biological implications of significance for shellfish themselves. The nonculturable human enteric viruses are responsible for most if not all of the illness transmitted by virus-carrying shellfish. Use of feces-associated natural virus in numbers comparable to those found in grossly polluted waters has been instrumental in developing new perspectives of virus carriage and its biological significance. The feasibility of developing a virus standard for virus surveillance of shellfish and its use for assessment of health risks which aris as a consequence of shellfish virus carriage is discussed.     

PCB levels in surface and waste waters in Egypt

Samples of surface water from the river Nile, Ismailia and El-Mahmodia Canals, and waste waters from eight plants were collected and analysed for determination of PCB levels. The mean concentrations of PCBs in River Nile, Ismailia Canal, El-Mahmodia Canal, and waste waters were 24 ± 14, 39 ± 18, and 170 ± 150 ng/L, respectively. The waste waters discharged from industrial plants were found to increase the levels of PCBs in surface waters. The concentrations of PCBs in the River Nile and two Canals are within the range found in the Hudson, Avon, and Frome Rivers, and for the Northern Mississippi area.     

Abnormal high natural radium concentration in surface waters

Unexpected high 228Ra concentrations, up to 2 Bq 1(-1), were found in waters of a coastal lagoon close to a monazite sand separation plant. Due to their use as process waters in this plant, the initial supposition was a contamination related to its operation. However, it was concluded that these abnormal radium concentrations had a natural origin, springs at the lagoon head area with high 228Ra and 226Ra concentrations. The strong relationship among radium and light rare-earth elements (LREEs), the observed 228Ra/226Ra activity ratio and the rare-earth element pattern in the spring waters suggested that monazite is the main source of nuclides for water, indicating the disturbance of monazite chemical stability by the combined effects of low pH and high salinity. Both factors combined allow relatively low mobility of thorium, but, on the other hand, a relatively high mobility of radium and LREEs.     

Tritium in surface waters of the Yenisei River basin

This paper reports an investigation of the tritium content in the surface waters of the Yenisei River basin near the Mining and Chemical Combine (MCC). In 2001 the maximum tritium concentration in the Yenisei River did not exceed 4 +/- 1 Bq l(-1), which is consistent with the data of 1998-99. However, it has been found that there are surface waters containing enhanced tritium as compared with the background values for the Yenisei River. For instance, in the Ploskii Stream and the Shumikha River the maximum tritium concentrations amount to 168 and 81 Bq l(-1), respectively. The source of tritium in these surface waters is the last operating reactor at the MCC, which still uses the Yenisei water as coolant. In water and sediment samples of the Bolshaya Tel River (a tributary of the Yenisei River) the tritium content turned out to be at least 10 times higher than the background values for the Yenisei River. The measurements conducted at the RPA RADON (Moscow) revealed not only tritium but also the artificial radionuclide (14)C in the Bolshaya Tel samples. The data obtained suggest that the Bolshaya Tel River receives the major part of tritium from sediments rather than from the water catchment area. This allows the conclusion that there is water exchange between the surface waters and the radioactively contaminated underground horizons of the "Severny" testing site.     

Chlorpyrifos in surface waters before and after a federally mandated ban

Samples collected from rural and urban streams in the City of Denton, Texas, USA were analyzed for the organophosphorus pesticides diazinon and chlorpyrifos during the years preceding and following a United States Environmental Protection Agency ban on many chlorpyrifos uses. A network of 70 monitoring stations, based mainly on topography and hydrological considerations, were established within the three main watersheds of Denton. Monitoring stations were sampled monthly from March through August during periods of normal flow (baseflow), resulting in a total of 308 samples and 311 samples collected during 2001 and 2002, respectively. Pesticide concentrations were determined using commercially available enzyme-linked immunosorbent assays (ELISA) specific for each pesticide. Results from this temporally and spatially dense monitoring effort were used to illustrate the impacts of a ban on most chlorpyrifos sales that was imposed in December 2001. The total number of samples exhibiting concentrations above method lower limits of detection (LLD) decreased between 2001 and 2002 for both chlorpyrifos and diazinon. The total number of sites exhibiting at least one sample with concentrations above the LLD for chlorpyrifos, however, significantly decreased (Fisher's exact test, p<0.0001, n=70) when comparing 2001 (before the ban) with 2002 (after the ban). Similar analyses indicated no significant difference (Fisher's exact test, p=0.50, n=70) in the number of sites exhibiting detectable diazinon concentration between 2001 and 2002. Our results indicate that the cessation of retail chlorpyrifos sales at the end of 2001 resulted in a highly significant decrease in the surface water occurrences of this pesticide during 2002.     

Radiocesium in North San Francisco Bay and Baja California coastal surface waters

Radiocesium, 137Cs, and rare earth elements (REEs) were determined in suspended material and dissolved fractions of waters across the salinity gradient in North San Francisco Bay (estuary). We describe the variation of this conservative isotope tracer with salinity and sediment load. REE data are used to differentiate marine and terrigenous source terrains for suspended material and dissolved fractions. We estimate that about 1-4 x 10(10) Bq of 137Cs migrates annually on suspended material through the North Bay. In addition, 137Cs concentrations were measured in surface waters off Baja California. Combined in situ water density (sigma(t)) and 137Cs data distinguish between California Current and Gulf of California water, and delineate areas of upwelling, where nutrient-rich, deep Pacific Intermediate water, with little or no 137Cs, is brought to the surface off promontories along Baja California.     

Viruses in wastewaters

Viruses of animals, plants, and bacteria abound in sewage and receiving waters. Their ecological impact has, for the most part, gone unheeded except as it relates to viruses from human sources. Viruses present at levels infective to man have been recovered from waters used for recreational or drinking purposes. Their presence in a water environment virtually always denotes prior contamination by domestic wastes. Neither conventional sewage treatment processes nor the discharge to land or water of sludges produced by these processes achieve full viral control. Many environmental virologists advocate the setting of permissible virus limits for those recreational and potable waters dominated by wastewater effluents. The initiation of regulatory pressure to restrict virus discharges into these water environments has been instituted in Montgomery County, Maryland, and in the states of California and Arizona.     

Viruses in groundwaters

There is no longer any question as to the presence of human enteroviruses in secondary sewage effluents. Sufficient data are available to indicate that viruses can and do percolate through the soil and move with the groundwater. Also, there is no question that a significant number of human illnesses of viral etiology have been associated with the consumption of untreated or chlorinated groundwater obtained from sewage contaminated wells. Although classical epidemiological investigative evidence linking groundwater with enterovirus disease transmission is not currently available, the alternative data presented in this report indicate that virus in groundwater is of sufficient significance to public health to warrant increased viral surveillance of groundwater. Concurrently, efforts should be directed toward increasing enterovirus disease surveillance and reporting to facilitate the earliest possible recognition of an outbreak and the initiation of an epidemiological investigation. Only under these conditions will the magnitude of the significance of viruses in groundwater be elicited.     

Viruses in wastewater aerosols

Agricultural land application of wastewater is becoming a widely used means of dealing with water scarcity and diminishing sources of unpolluted water. One of the most common forms of land application—sprinkler irrigation—poses an environmental problems in that it created wastewater aerosols. Air sampling experiments done at distances of up to 100 meters from wastewater irrigation sprinklers have detected several airborne enteroviruses: echovirus 1, 25, 29; poliovirus II, and coxsackie B1. The levels of airborne viruses found in wastewater aerosols may be potentially hazardous at any level. Since the impact of these findings on public health is not clear, epidemiological investigations by standard techniques should be conducted. It is estimated that the number of viruses isolated in environmental samples may be smaller by one or two orders of magnitude (90%–99%) than their actual number due to the limitations of virus recovery procedures. The unvailability of a reliable indicator microorganism which fulfills all the requirements for a biological indicator also makes it difficult to determine the virus level in the aerosols. Thus the scientific knowledge available today is insufficient to determine with certainty that no public health risk is created by wastewater aerosols. A comprehensive prospective study will, in all likelihood, provide answers to most questions and make it possible to assess more reliably the extent of the health risk due to wastewater aerosols.     

Perfluorinated compounds in surface waters from Northern China: Comparison to level of industrialization

Inclusion of Perfluorooctane Sulfonate (PFOS) in the Stockholm Convention because of its exemptions, has resulted in increased annual production of PFOS-containing chemicals in China to accommodate domestic and overseas demands. Accordingly, concern about environmental contamination with perfluorinated compounds (PFCs), such as PFOS, has arisen. However, little information is available on the status and trends in the distribution, sources or risk of PFCs in aquatic environments of China. In the present study, forty two surface water samples collected from five regions with different levels of industrialization were monitored for concentrations of PFCs by use of solid phase extraction and LC/MS/MS. Mean concentrations (maximum concentration) of PFOA and PFOS, which were the dominant PFCs, were 1.2 (2.3) and 0.16 (0.52) ng/l for Guanting, 1.2 (1.8) and 0.32 (1.1) ng/l for Hohhot, 2.7 (15) and 0.93 (5.7) ng/l for Shanxi, 6.8 (12) and 2.6 (11) ng/l for Tianjin, 27 (82) and 4.7 (31) ng/l for Liaoning, respectively. The greatest concentrations of PFCs (121 ng/l), PFOA (82 ng/l) and PFOS (31 ng/l) were observed in Liaoning, which might originate from tributaries of the Liaohe River, the most polluted watershed in Northeast China. While, concentrations of PFCs in the Guanting and Hohhot regions were 3 to 20 fold less than those from Tianjin and Liaoning. This result is consistent with little contribution of PFCs being released from agricultural and non-industrial activities. The magnitudes of mass flow for PFOA and PFOS in decreasing order were: Guanting < Hohhot < Tianjin < Liaoning < Shanxi and Guanting < Hohhot < Shanxi < Tianjin < Liaoning. The larger mass flows of PFOS were accompanied by relatively larger magnitudes of PFOA. Concentrations of both PFOA and PFOS in waters from all regions were less than suggested allowable concentrations. However, the relatively greater concentrations of PFCs in Tianjin and Liaoning suggest that further studies characterizing their sources and potential risk to both humans and wildlife are needed.     

Impacts of climate change on surface water quality in relation to drinking water production

Besides climate change impacts on water availability and hydrological risks, the consequences on water quality is just beginning to be studied. This review aims at proposing a synthesis of the most recent existing interdisciplinary literature on the topic. After a short presentation about the role of the main factors (warming and consequences of extreme events) explaining climate change effects on water quality, the focus will be on two main points. First, the impacts on water quality of resources (rivers and lakes) modifying parameters values (physico-chemical parameters, micropollutants and biological parameters) are considered. Then, the expected impacts on drinking water production and quality of supplied water are discussed. The main conclusion which can be drawn is that a degradation trend of drinking water quality in the context of climate change leads to an increase of at risk situations related to potential health impact.     

Organochlorine and organophosphorous pesticide residues in ground water and surface waters of Kanpur, Uttar Pradesh, India

A survey undertaken in Kanpur, northern India, has shown the presence of high concentrations of both organochlorine and organophosphorous pesticides in the surface and ground water samples. Liquid-liquid extraction followed by GC-ECD was used for the determination of these compounds. Among the various pesticides analyzed, high concentrations of gamma-HCH (0.259 microg/l) and malathion (2.618 microg/l) were detected in the surface water samples collected from the River Ganges in Kanpur. In the ground water samples collected from the various hand pumps located in agricultural and industrial areas, apart from gamma-HCH and malathion, dieldrin was also detected. The maximum concentration values of gamma-HCH, malathion and dieldrin were 0.900, 29.835 and 16.227 microg/l, respectively. Especially, the concentration of malathion was found to be much higher than the EC water quality standards in the ground water samples from industrial area posing a high risk to the common people. Pesticides like DDE, DDT, aldrin, ethion, methyl parathion and endosulfan were not detected in both the surface and ground water samples.     

Triclosan in waste and surface waters from the upper Detroit River by liquid chromatography-electrospray-tandem quadrupole mass spectrometry

Triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol) is an antimicroibial disinfectant agent used in a wide array of consumer products. An analytical method based on solid-phase extraction (SPE) followed by reverse phase, liquid chromatography coupled with electrospray ionization (negative)-tandem quadrupole mass spectrometry (LC-ESI(-)-MS/MS; in the multiple reaction monitoring (MRM) mode) was developed, optimized and validated for the determination of triclosan in wastewater/sewage treatment plant (WSTP) effluent and surface waters from the upper Detroit River (Canada). The mean recoveries (+/-%RSD) of triclosan and the internal standard 2'-HO-tribromodiphenyl ether (2'-HO-BDE-28) spiked to surface water and WSTP effluent samples ranged similarly from 104+/-8% and 91+/-10%, respectively, and method limits of quantification were in the low ppb/high ppt range. However, ESI(-) enhancement was found for both analytes due to sample matrix effects, as indicated by % process efficiencies (a measure of ESI(-) enhancement/suppression), which were in the 111-128% range. We report the first known assessment of triclosan in the Detroit River watershed of the Great Lakes, which preliminarily examined the presence and UV-treatment effects on triclosan in effluent from the major WSTP serving the City of Windsor, Ontario, Canada, and fate in surface waters of the upper Detroit River. Triclosan in WSTP effluent decreased 22% after final UV treatment to a mean concentration of 63 ng/L. Concentrations were further reduced to 4 and 8 ng/L (a >90% reduction) in surface water samples from sites downstream on the Canadian shoreline of the Detroit River, which was due to dilution. Two hydroxylated tribrominated diphenyl ethers, which are structurally similar to triclosan, were also detected in WSTP effluent and surface water samples.     

Simultaneous biological removal of endosulfan (alpha+beta) and nitrates from drinking waters using wheat straw as substrate

Nitrate and endosulfan (alpha+beta) removal was studied in an upflow biological denitrification reactor packed with wheat straw as carbon source and support particles for microorganisms. While almost complete nitrate elimination and between 65% and 70% endosulfan (alpha+beta) elimination occurred when the temperature was higher than 20 degrees C; below that value, nitrate removal efficiency decreased to about 10%. Nitrate, dissolved organic carbon (DOC), and endosulfan (alpha+beta) removal efficiencies decreased considerably at 1500 microg/l endosulfan concentration in the batch experiments. Although a high removal efficiency was observed for endosulfan (alpha+beta) and nitrate in the biological denitrification continuous reactor, the effluent water could not be used for drinking purpose because of the unacceptable levels of endosulfan (alpha+beta), colour and dissolved organic content. During the continuous study, 23.4% of the initial weight of wheat straw was lost and 24 g was consumed per gram of nitrogen removed. The results of the continuous study showed that 21.3% of the endosulfan removal was achieved by adsorption onto the wheat straw and 68.2% of the endosulfan removal occurred by biological activity and the remaining portion was detected in the effluent water.     

Characterization of natural organic matter from eight Norwegian surface waters: Proton and copper binding

As a part of the International NOM-Typing Project, proton and copper binding studies were conducted on ultrafiltered (>1000 dal.) and dialysed (>100 dal.) natural organic matter (NOM) samples from eight Norwegian Lakes. The NOM samples were similar with respect to proton and copper binding, although minor differences were observed among the samples of different origin. Slight variations occurred for seasonal changes and lime additions. The proton binding pK_a values grouped in three distinct classes: pK_a1 = 4.20–4.28; pK_a2 = 6.61–6.87; and pK_a3 = 9.27–9.8. The average total proton binding site concentration of the NOM samples was: 12.7 meq/g total organic carbon (TOC). Two binding sites were established for copper with average log K1 = 4.84 and log K2 = 7.17. The average site concentration for samples isolated by reverse osmosis (RO) was 0.56 μmol/mg C. Copper binding characteristics appear to be influenced by the method of sample isolation. For NOM isolated by low pressure evaporation (evap), binding site concentrations are smaller, conditional stability constants are higher, variability of the copper complexation capacity is smaller, and correlation with elemental composition (C, N, H) is better than in the case of NOM isolated by RO.     

Estrogen-, androgen- and aryl hydrocarbon receptor mediated activities in passive and composite samples from municipal waste and surface waters

Passive and composite sampling in combination with in vitro bioassays and identification and quantification of individual chemicals were applied to characterize pollution by compounds with several specific modes of action in urban area in the basin of two rivers, with 400,000 inhabitants and a variety of industrial activities. Two types of passive samplers, semipermeable membrane devices (SPMD) for hydrophobic contaminants and polar organic chemical integrative samplers (POCIS) for polar compounds such as pesticides and pharmaceuticals, were used to sample wastewater treatment plant (WWTP) influent and effluent as well as rivers upstream and downstream of the urban complex and the WWTP. Compounds with endocrine disruptive potency were detected in river water and WWTP influent and effluent. Year-round, monthly assessment of waste waters by bioassays documented estrogenic, androgenic and dioxin-like potency as well as cytotoxicity in influent waters of the WWTP and allowed characterization of seasonal variability of these biological potentials in waste waters. The WWTP effectively removed cytotoxic compounds, xenoestrogens and xenoandrogens. There was significant variability in treatment efficiency of dioxin-like potency. The study indicates that the WWTP, despite its up-to-date technology, can contribute endocrine disrupting compounds to the river. Riverine samples exhibited dioxin-like, antiestrogenic and antiandrogenic potencies. The study design enabled characterization of effects of the urban complex and the WWTP on the river. Concentrations of PAHs and contaminants and specific biological potencies sampled by POCIS decreased as a function of distance from the city.     

Pollution studies on Nigerian rivers: The onset of lead pollution of surface waters in Ibadan

Lead levels in the waters and sediments of the lake of the International Institute of Tropical Agriculture, Agodi Lake, Oba Lake, at three stations on Ogunpa stream, and at three stations on Ona River were measured from October 1977 to June 1978, using the combined APDC-MIBK-flame atomic absorption spectrophotometry technique. The lead levels recorded ranged from 0.2 to 46 μg/L for the aqueous phases; however, the levels in the sediments were much higher, ranging from about 18 to 85 mg/kg (dry weight). Although there is nothing alarming about these levels, the levels of lead in water bodies located in areas with high traffic density were consistently higher than levels for comparable waters in low traffic density areas. Similarly, lead levels were significantly higher in the fresh sediments of water bodies in areas with high traffic density, clearly indicating the onset of lead pollution for those high traffic density areas.     

Pollution studies on Nigerian rivers: Toxic heavy metal status of surface waters in Ibadan City

The levels of the heavy elements cadmium, copper, cobalt, iron, manganese, nickel, lead, and zinc in the major streams and man-made lakes in and around Ibadan City were determined at roughly two monthly intervals between August 1977 and February 1979. They were found to be in the ppb and sub-ppb level except for iron and manganese which were in the ppm range. To assess the quality of these waters with respect to heavy metal contamination, a comparison is made between our results, world averages for both freshwater and seawater, and international water quality standards for drinking water. All elements, except iron manganese, were well within the safety limits. The low level of industrialization in Ibadan has kept its streams and lakes relatively free from heavy metal contamination.     

Assessment of surface waters acidification as indicated by zooplankton in the taiga zone of Northern European Russia

Published results of comprehensive hydrochemical and hydrobiological studies of water bodies in the taiga zone of northwestern Russia were analyzed to estimate the lowest values of water pH at which individual zooplankton species had been recorded. On this basis, the most significant species indicative of surface water acidification were identified and a scale of their distribution depending on the degree of acidification was compiled.     

Transport of plutonium in surface and sub-surface waters from the Arctic shelf to the North Pole via the Lomonosov Ridge

New data on the levels and long-range transport of plutonium in the Arctic Ocean, recorded in the course of two expeditions to this zone in 1994 and 1996, are discussed in this paper. Specifically, approximately 100 plutonium measurements in surface and sub-surface water sampled at 58 separate stations throughout the Kara, Laptev and East Siberian Seas, as well as along latitudinal transects across the Lomonosov Ridge, are reported and interpreted in terms of the circulation pathways responsible for the transport of this element from the North Atlantic to the Arctic Shelf and into the Arctic interior. In addition, the behaviour of plutonium in its transit through the vast Arctic shelf seas to open waters under extreme environmental conditions is discussed in terms of the partitioning of plutonium between filtered (<0.45 microm) seawater and suspended particulate, and its association with colloidal matter. Finally, limited evidence of the presence of a colloidal plutonium component in Arctic waters subject to direct riverine input is adduced.