Environmental effects of water resource development and use in the Tarim River basin of northwestern China

The unbridled development and use of water resources in the Tarim River basin over the last 50 years have led to a serious degradation of soil (>12×10³ km² of land desertified between the 1960s and 1990s) and water quality (rise in maximum salinity was from 1.3 g l^–1 in 1960, to 4.0 g l^–1 in 1981–1984, and to 7.8 g l^–1 in 1998). Approximately 300 km of the lower reaches of the river course dried up between the 1950s and 1970s, seriously altering the downstream hydrological processes (a 4–6 m drop in groundwater levels from the 1960s to the 1980s, and 0.2 m yr^–1 thereafter) and ecosystems (67% and 50% decrease (1958–1978) in Populus euphratica forest acreage and biomass, respectively). Between the 1950s and 1990s, 3820 km² of P. euphratica forest and 200 km² of shrub- and grassland were lost in the lower reaches of the Tarim River. In this study, based on estimates of soil organic carbon in desertified lands, it has been found that in the last 30 years (1970–2000), approximately 112 Tg of organic carbon (28% originating in the 0–1.0 m soil profile) has been released into the atmosphere as a result of soil degradation in the Tarim River basin. Intensive anthropogenic disturbance has been one of the foremost factors leading to the deterioration of water resources in this region. The key to solving these problems is to enhance the scientific and technical level of monitoring, management, and restoration of water resources and associated water and soil components of local ecosystems.     

Recharge processes in karstic systems investigated through the correlation of chemical and isotopic composition of rain and spring-waters

Four karstic springs in southern France, along with rainwater in the same area, were monitored during two hydrological cycles. Stable isotopic ratios (δ¹⁸O and δD) allow the contribution of the rain waters from the previous periods (discretised as winter or summer period) to the spring water to be estimated. These computations indicate that heavy rainfall events during the autumn season contribute for 56 ± 7% and 68 ± 9% of the spring water discharge during the following winter and summer seasons, respectively. During the low flow period, residence time does not exceed 1 hydrological cycle, for a large part of the water.Stable isotopic ratios (δ¹⁸O and δD) combined with Cl concentration allow the evapotranspiration coefficients to be estimated although the recharge surface is not known and hydrological balance can not be computed. Except for one spring, the evapotranspiration coefficients range from 0.54 to 0.38 (46–62% volume reduction), even during the high flow period.The short residence times, and the strong evapotranspiration coefficients whatever the period (winter or summer) are interpreted as the result of the major role of the epikarst reservoir in the karst recharge functioning over direct or diffuse infiltration.     

Environmental impact of an urban landfill on a coastal aquifer (El Jadida, Morocco)

The El Jadida landfill is one among many uncontrolled dumping sites in Morocco with no bottom liner. About 150 tons/day of solid wastes from mixed urban and industrial origins are placed directly on the ground. At the site of this landfill, the groundwaters circulate deeply (10–15 m) in the Cenomanian rock (calcareous–marl), which is characterised by an important permeability from cracks. The soil is sand–clay characterized by a weak coefficient of retention.The phreatic water ascends to the bottom of three quarries, which are located within the landfill. These circumstances, along with the lack of a leachate collection system, worsen the risks for a potential deterioration of the aquifer.To evaluate groundwater pollution due to this urban landfill, piezometric level and geochemical analyses have been monitored since 1999 on 60 wells. The landfill leachate has been collected from the three quarries that are located within the landfill. The average results of geochemical analyses show an important polluant charge vehiculed by landfill leachate (chloride = 5680 mg l⁻¹, chemical oxygen demand = 1000 mg l⁻¹, iron = 23 000 μg l⁻¹). They show also an important qualitative degradation of the groundwater, especially in the parts situated in the down gradient area and in direct proximity to the landfill. In these polluted zones, we have observed the following values: higher than 4.5 mS cm⁻¹ in electric conductivity, 1620 and 1000 mg l⁻¹ respectively in chlorides and sulfate (), 15–25 μg l⁻¹ in cadmium, and 60–100 μg l⁻¹ in chromium. These concentrations widely exceed the standard values for potable water.Several determining factors in the evolution of groundwater contamination have been highlighted, such as (1) depth of the water table, (2) permeability of soil and unsaturated zone, (3) effective infiltration, (4) humidity and (5) absence of a system for leachate drainage. So, to reduce the pollution risks of the groundwater, it is necessary to set a system of collection, drainage and treatment of landfill leachates and to emplace an impermeable surface at the site of landfill, in order to limit the infiltration of leachate.     

Distribution of phosphorus along the Delaware,an urbanized coastal plain estuary

The Delaware Estuary is heavily urbanized with elevated concentrations of phosphorus from industrial and municipal inputs. For 24 research cruises during 1986–1988, total phosphorus (TP) concentration was highest near maximum inputs in the tidal river and at low salinity where turbidity was maximal. In these contiguous regions, average TP concentration over the study period was 5.3–6.1 μM. Downstream of the TP peak in the high turbidity zone of the estuary, TP decreased to minimum concentrations (1.3–1.5 μM) near the mouth of Delaware Bay. Distributions of dissolved reactive (DRP), dissolved organic (DOP), and particulate (PP) phosphorus along the estuary reflected spatial and temporal patterns in phosphorus inputs, turbidity, river flow, and biological production. In the river, DRP was 2–4 μM (51–65% of TP) and inversely related to river flow. PP, although enriched in the river (1–3 μM), was highest (>4 μM) in the turbidity maximum at low salinity. In the bay, distributions of DRP, PP, and DOP were all linked, in different ways, to biological production. The dependence of DOP on production was, however, complex and affected by DRP concentrations. During the past 30 yr, there has been a fourfold decrease in TP concentrations in the tidal river of the Delaware Estuary. This dramatic decrease in TP, however, is contrasted by an apparent increase in DRP concentration over the past 12 yr. This apparent increase in DRP may be linked to improved water quality (e.g., higher pH) in the river over the past decade.     

Geostatistical analysis of arsenic concentration in groundwater in Bangladesh using disjunctive kriging

The National Hydrochemical Survey of Bangladesh sampled the water from 3,534 tube wells for arsenic throughout most of Bangladesh. It showed that 27% of the shallow tube wells (less than 150 m deep) and 1% of the deep tube wells (more than 150 m deep) exceeded the Bangladesh standard for arsenic in drinking water (50 µg L^–1). Statistical analyses revealed the main characteristics of the arsenic distribution. Concentrations ranged from less than the detection limit (0.5 µg L^–1), to as much as 1,600 µg L^–1, though with a very skewed distribution, and with spatial dependence extending to some 180 km. Disjunctive kriging was used to estimate concentrations of arsenic in the shallow ground water and to map the probability that the national limit for arsenic in drinking water was exceeded for most of the country (the Chittagong Hill Tracts and the southern coastal region were excluded). A clear regional pattern was identified, with large probabilities in the south of the country and small probabilities in much of the north including the Pleistocene Tracts. Using these probabilities, it was estimated that approximately 35 million people are exposed to arsenic concentrations in groundwater exceeding 50 µg L^–1 and 57 million people are exposed to concentrations exceeding 10 µg L^–1 (the WHO guideline value).     

The role of supergene sulphuric acid during weathering in small river catchments in low mountain ranges of Central Europe: Implications for calculating the atmospheric CO2 budget

The geochemistry of dissolved and suspended loads in river catchments of two low mountain ranges in Central Europe allows comparison of pertinent chemical weathering rates. Distinct differences in lithology, i.e. granites prevailing in the Black Forest compared to Palaeozoic sediments in the Rhenish Massif, provide the possibility to examine the influence of lithology on weathering. Here we determine the origin of river water using the stable isotope ratio δ¹⁸O_H2O and we quantify the geogenic proportions of sulphate from stable isotope ratios δ³⁴S_SO4 and δ¹⁸O_SO4. Particularly in catchments with abundant pyrite, determination of the geogenic amount of sulphate is important, since oxidation of pyrite leads to acidity, which increases weathering. Our results show that spatially averaged silicate weathering rates are higher for the river catchments Acher and Gutach in the Black Forest (10–12 t/km²/yr) compared to the river catchments of the Möhne dam and the Aabach dam in the Rhenish Massif (2–6 t/km²/yr). Correspondingly, the CO₂ consumption by silicate weathering in the Black Forest (334–395 × 10³ mol/km²/yr) is more than twice as high as in the Rhenish Massif (28–151 × 10³ mol/km²/yr). These higher rates for watersheds of the Black Forest are likely due to steeper slopes leading to higher mechanical erosion with respective higher amounts of fresh unweathered rock particulates and due to the fact that the sediments in the Rhenish Massif have already passed through at least one erosion cycle. Carbonate weathering rates vary between 12 and 38 t/km²/yr in the catchments of the Rhenish Massif. The contribution of sulphuric acid to the silicate weathering is higher in the catchments of the Rhenish Massif (9–16%) than in the catchments of the Black Forest (5–7%) due to abundant pyrite in the sediments of the Rhenish Massif. Three times higher long-term erosion rates derived from cosmogenic nuclides compared to short-term erosion rates derived from river loads in Central Europe point to three times higher CO₂ consumption during the past 10³ to 10⁴ years.     

Arsenic in the groundwater of Ouro Preto (Brazil): its temporal behavior as influenced by the hydric regime and hydrogeology

In the city of Ouro Preto (MG), water catchment for public supply originates from superficial drainage, springs, old abandoned mines and some driven wells. In the rocks of the region, As is originally found in gold-enriched sulphide-bearing mineral deposits. The weathering process introduces As into the hydrological system by dissolution of this element into the leachate. Measurement of the As content in the groundwater of some catchments was carried out during 1 year and these measurements demonstrated high As content—up to 224 μg L⁻¹ of As(V)—during the rainy season (the maximum concentration limit according to World Health Organization is 10 μg L⁻¹). Lower values were observed during the dry season and in some sampling stations, As was not even detected. The As concentration variability during 1 year shows a strict and direct relationship to seasonal and hydrological conditions. For city authorities, responsible for public water supply, it is necessary to perform a complete inventory of the water sources used and constantly monitor the As content in the water.     

Lake Suwa — Eutrophication and its partial recent recovery

Lake Suwa, located in the center of the largest Japanese island of Honshu was a typical hypertrophic lake with a dense scum Microcystis species in summer during the 1970's. However, due to the introduction of a sewage treatment plant and the awareness of environmental pollution by local residents, a decrease in the concentration of nutrients in lake water since 1981 has been observed (from 1600 g l^–1 and 160 g l^–1 in 1977 to 990 g l^–1 and 110 g l^–1 in 1984 for total nitrogen and phosphorus respectively).     

Separation of groundwater-flow components in a karstified aquifer using environmental tracers

Groundwater discharges from the intensively karstified Taurus Mountains to the Mediterranean Sea, either along the contact zone between the mountains and the Travertine Plateau (the Kirkgozler Springs, 15 m³/s), or through the travertine (e.g. the Dudenbasi Spring, 18 m³/s) and underneath it (unnamed submarine springs, unknown discharges). In an attempt to identify the hydraulic connections between the various outlet points, groundwater was analyzed for stable and radioactive isotopes, CFCs and He. The upgradient springs, belonging to the Kirkgozler–Dudenbasi system, were proven to be a mixture of recent and older water on the basis of their low ¹⁴C values (12–22.4 pmc), their exceptionally high He content (429–991 μcc/kg) and ³He:⁴He (R:Ra) ratios (1.471–2.602) and their measurable ³H and CFC contents (1.9–5.9 TU and 0.84 to 3.27 pmoles/kg, respectively). The older component probably contains an even lower amount of modern C. However, the undersaturation of the mixture with respect to calcite, its high CO₂ content (up to 83 mg/L) and its enriched ¹³C values (−2.2 to −4.1‰) suggest intensive water/rock interactions, which would contribute ¹⁴C-devoid bicarbonates to the solution. Downgradient springs discharging along the Mediterranean coast contain groundwater contributions from higher altitudes, as evidenced by their depleted δ¹⁸O and δD composition with respect to the local precipitation; however, a larger portion of the recent water component could be contributed from direct precipitation on the travertine. This larger component is reflected in the increased ³H (3.4 to 8.4 TU) and ¹⁴C (32.7–63.6 pmc) contents, atmospheric He (43–82 pmoles/kg), R:Ra values (1.006–1.198) and CFC contamination of the water.     

Laminated tufa sediments formed from overflow karst springs: Controls on their deposition and carbon–oxygen isotope records

Tufa sediments are freshwater carbonates that precipitate in karst regions after degassing of carbon dioxide from groundwater in contact with the atmosphere. When laminated, these carbonates can provide high‐resolution records for the study of climate, hydrological and environmental conditions at the time of their precipitation. The formation of these carbonates directly depends on the hydrological regime, and in karst regions discontinuous discharges are often recorded. This study investigates the record of recent laminated tufa sediments precipitated downstream overflow springs in Trabaque Canyon (central Spain). The hydrological dynamics of the karst system were monitored for over three years and a stable isotope record was obtained from laminated tufa carbonates precipitated from an overflow spring. Additionally, a hydrological model of overflow springs was generated and a tufa δ¹⁸O record under constrained parameters was simulated. Temperature is the dominant control of the variation in tufa δ¹³C and δ¹⁸O values within each lamina, although when comparing different laminae, δ¹³C_DIC and δ¹⁸O of river water are also major controls. The positive correlation between tufa δ¹³C values and water temperature is caused by the fractionation occurred by carbon dioxide degassing due to the thermal dependence of carbon dioxide solubility. Additionally, the system recorded a temperature‐independent degassing process caused by the large gradient between groundwater and atmospheric carbon dioxide that is limited to the proximity of the spring. This study cautions on the risk of assuming continuous deposition when studying laminated tufa sediments and highlights the potential of their stable isotope records to provide hydrological information of their aquifers during the past.     

A preliminary investigation into the use of ochre as a remedial amendment in arsenic-contaminated soils

Ochre is an unwanted waste product that accumulates in wetlands and streams draining abandoned coal and metal mines. A potential commercial use for ochre is to remediate As contaminated soil. Arsenic contaminated soil (605 mg kg⁻¹) was mixed with different ochres (A, B and C) in a mass ratio of 1:1 and shaken in 20 mL of deionised water. After 72 h As concentration in solution was ca. 500 μg kg⁻¹ in the control and 1–2.5 μg kg⁻¹ in the ochre treated experiments. In a second experiment soil:ochre mixtures of 0.05–1:1 were shaken in 20 mL of deionised water for 24 h. For Ochres A and C, as solution concentration was reduced to ca. 1 μg kg⁻¹ by 0.2–1:1 ochre:soil mixtures. For Ochre B, as concentration only reached ca. 1 μg kg⁻¹ in the 1:1 ochre:soil mix. Sorption of As was best modelled by a Freundlich isotherm using As sorption per mass of goethite in the ochre (log K = 1.64, n = 0.79, R² = 0.76, p 0.001). Efficiency of ochre in removing As from solution increased with increasing total Fe, goethite, citrate dithionite extractable Fe and surface area.     

Carbon sources and signals through time in an Alpine groundwater Basin, Sagehen California

In 2003, chlorofluorocarbon (CFC) apparent ages, major ion chemistry and C isotopes were determined in nine springs from Sagehen Basin, a high elevation watershed in the eastern Sierra Nevada. Springs with similar apparent ages, which ranged between 15 and 45 a, had very similar chemistry despite being found in different areas of the watershed. In agreement with earlier studies, concentrations of rock-derived cations (Ca²⁺ and Na⁺), conductivity, temperature and pH increase with apparent age, documenting the chemical evolution of this groundwater system. In contrast with the cation data, δ¹³C and ΣCO₂ show no correlation with apparent age. δ¹³C displays a strong linear relationship with 1/ΣCO₂ (R² = 0.91). This is consistent with results from a previously developed soil respiration/diffusion model. Spring radiocarbon content ranged between 85 and 110 pmc and varied with apparent age, whereby the youngest groundwater has the highest radiocarbon values. The spring radiocarbon is set by the soil pCO₂ and its trend can be best described assuming the soil CO₂ is composed of a mixture of 50–66% fast- (15–25 a) and 33–50% slow- (4 ka) cycling components. These results are consistent with previous soil C studies. The C isotope data indicate that in Sagehen Basin the groundwater ΣCO₂ is inherited from the soil zone with little, if any, contribution from the dissolution of disseminated calcite.     

Dolomite Versus Calcite Weathering in Hydrogeochemically Diverse Watersheds Established on Bedded Carbonates (Sava and So?a Rivers, Slovenia)

The relative contributions of dolomite to calcite weathering related to riverine fluxes are investigated on a highly resolved spatial scale in the diverse watersheds of Slovenia, which previous work has shown have some of the highest carbonate-weathering intensities in the world and suggests that dolomite weathering is favored over limestone weathering in mixed carbonate watersheds. The forested Sava and So?a River watersheds of Slovenia with their headwaters in the Julian Alps drain alpine regions with thin soils (<30 cm) and dinaric karst regions with thicker soils (0 to greater than 70 cm) all developed over bedded Mesozoic carbonates (limestone and dolomite), and siliclastic sediments is the ideal location for examining temperate zone carbonate weathering. This study extends previous work, presenting geochemical data on source springs and documenting downstream geochemical fluctuations within tributaries of the Sava and So?a Rivers. More refined sampling strategies of springs and discrete drainages permit directly linking the stream Mg²⁺/Ca²⁺ ratios to the local bedrock lithology and the HCO₃ ^? concentrations to the relative soil depths of the tributary drainages. Due to differences in carbonate source lithologies of springs and tributary streams, calcite and dolomite weathering end members can be identified. The Mg²⁺/Ca²⁺ ratio of the main channel of the Sava River indicates that the HCO₃ ^? concentration can be attributed to nearly equal proportions by mass of dolomite relative to calcite mineral weathering (e.g., Mg²⁺/Ca²⁺ mole ratio of 0.33). The HCO₃ ^? concentration and pCO₂ values increase as soil thickness and alluvium increase for discrete spring samples, which are near equilibrium with respect to calcite. Typically, this results in approximately 1.5 meq/l increase in HCO₃ ^? from the alpine to the dinaric karst regions. Streams in general do not change in HCO₃ ^?, Mg²⁺/Ca²⁺, or Mg²⁺/HCO₃ ^? concentrations down course, but warming and degassing of CO₂ produce high degrees of supersaturation with respect to calcite. Carbonate-weathering intensity (mmol/km²-s) is highest within the alpine regions where stream discharge values range widely to extreme values during spring snowmelt. Overall, the elemental fluxes of HCO₃ ^?, Ca²⁺, and Mg²⁺ from the tributary watersheds are proportional to the total water flux because carbonates dissolve rapidly to near equilibrium. Importantly, dolomite weathers preferentially over calcite except for pure limestone catchments.     

Lead in archaeological samples: an isotopic study by ICP-MS

Inductively coupled plasma mass spectrometry (ICP-MS) has been used to measure the concentration and isotopic composition of Pb in archaeological human and animal skeletal remains, soil from a village site of the Omaha tribe (U.S.A.) and cosmetic pigments.Lead concentrations in human bones from the Omaha tribe vary between 4.8 and 2570 μg/g, with younger people having the highest concentrations. Lead concentrations in animal bones from an Omaha village vary between 0.6 and 3.7 μg/g, and those of three soil samples range between 18 and 21 μg/g. Lead concentrations found in human bones from Anasazi (Utah, U.S.A.) and Alta (Peru) populations vary between 0.7 and 3.2 μg/g.Isotope ratios of a reagent grade Pb(NO₃)₂ solutions were measured by thermal ionization mass spectrometry (TIMS), as well as by ICP-MS to provide laboratory reference materials. The accuracy of the ICP-MS measurements relative to TIMS for the standard solution were found to be within 0.02–0.31% for²⁰⁶Pb/²⁰⁴Pb, 0.02–0.55% for²⁰⁷Pb/²⁰⁴Pb, and 0.16–0.56% for²⁰⁸Pb/²⁰⁴Pb. The precision of measurements on artifacts was 0.42–0.65% for²⁰⁶Pb/²⁰⁴Pb and 0.41–0.62% for²⁰⁷Pb/²⁰⁴Pb, whereas the precision for the same ratios for the bones was 0.85–1.8 and 0.82–1.67%, respectively. For the cosmetic lead-bearing pigments, a precision of 0.07–0.15% was found for both²⁰⁶Pb/²⁰⁴Pb and²⁰⁷Pb/²⁰⁴Pb ratios. Lead isotope ratios of artifacts give a radiogenic Pb signature, of which are close to signatures from PbZn mines of the central U.S. region. Lead isotope ratios of the pigments give non-radiogenic Pb signatures. Lead isotope ratios of the bones differ from those of the artifacts, and although similar in isotopic ratio to the pigments, they are more scattered, suggesting potential mixing of Pb from different regions.     

Karstological study of the new Kunming airport building area (Yunnan, China)

In Kunming area (6.8 mio population), two big interventions are in progress: construction of a new airport, the 23 km² area of which will extend across karst terrain northeast of the city, and extensive uptake of water from karst aquifers for drinking and agricultural use. In the study, an interdisciplinary approach was utilized to demonstrate the need for holistic karstology studies prior to performing extensive interferences in the karst environment. This study included survey of surface karst features and microscopic analyses of rock samples in the area of the new airport location, accompanied by hydrogeological studies and microbiological analyses of two karst drinking water sources in its vicinity (Qinglongdong, Huanglongdong). Results showed the specific characteristics of the subsoil stone forest that indicated a high level of karstification. The direction and characteristics of groundwater flow from the sinking Qiaotou Stream at the margin of the new airport area toward the Huanglongdong Spring were defined with a single tracer test. Additional information about hydrogeological characteristics of the karst aquifer was obtained by individual measurements of physical and chemical parameters of the springs and sinking stream. Selected chemical and bacteriological parameters showed substantial pollution of both springs due to various types of human activities in the catchments. The results of the study pointed to the necessity of taking immediate measures for the springs’ protection and showed the importance of interdisciplinary research when planning anthropogenic activities in the karst.     

Geomorphic controls on mercury accumulation in soils from a historically mined watershed, Central California Coast Range, USA

Historic Hg mining in the Cache Creek watershed in the Central California Coast Range has contributed to the downstream transport of Hg to the San Francisco Bay-Delta. Different aspects of Hg mobilization in soils, including pedogenesis, fluvial redistribution of sediment, volatilization and eolian transport were considered. The greatest soil concentrations (>30 mg Hg kg⁻¹) in Cache Creek are associated with mineralized serpentinite, the host rock for Hg deposits. Upland soils with non-mineralized serpentine and sedimentary parent material also had elevated concentrations (0.9–3.7 mg Hg kg⁻¹) relative to the average concentration in the region and throughout the conterminous United States (0.06 mg kg⁻¹). Erosion of soil and destabilized rock and mobilization of tailings and calcines into surrounding streams have contributed to Hg-rich alluvial soil forming in wetlands and floodplains. The concentration of Hg in floodplain sediment shows sediment dispersion from low-order catchments (5.6–9.6 mg Hg kg⁻¹ in Sulphur Creek; 0.5–61 mg Hg kg⁻¹ in Davis Creek) to Cache Creek (0.1–0.4 mg Hg kg⁻¹). These sediments, deposited onto the floodplain during high-flow storm events, yield elevated Hg concentrations (0.2–55 mg Hg kg⁻¹) in alluvial soils in upland watersheds. Alluvial soils within the Cache Creek watershed accumulate Hg from upstream mining areas, with concentrations between 0.06 and 0.22 mg Hg kg⁻¹ measured in soils 90 km downstream from Hg mining areas. Alluvial soils have accumulated Hg released through historic mining activities, remobilizing this Hg to streams as the soils erode.     

Geochemistry and genesis of brine emanations from Cretaceous strata of the Mamfe Basin, Cameroon

The geochemistry of 5 salt springs in the southwestern Mamfe Basin was investigated in order to infer the mineral content of their source and to relate the genesis of the springs to the local geology. Field observations revealed that, they are cold springs (23–28 °C), and are composed of secondary brines that are neutral to alkaline with pH values ranging from 7 to 8.7. Results of chemical analysis show that the springs contain major ions that form evaporite minerals, as well as chalcophile elements. The dominant cation is Na⁺ (>96%), and the dominant anion is Cl⁻ (>99%). Based on correlation coefficients between ions that form evaporites and field occurrence of efflorescences of halite, it is suggested that the ancient evaporites in the Mamfe Basin are composed entirely of carbonate and chloride salts. Meteoric and convective fluid flow processes are responsible for the dissolution of ancient evaporites and subsequent migration of brines to the surface from underground. The brines migrate through permeable strata with migration pathways resulting from a combination of fracture porosity created by post––Cretaceous tectonism and intergranular porosity enhanced by the chemically aggressive migrating brines.     

Ecological studies on the Kerhni reservoir (N-Greece)

This paper refers to the morphometric and hydrological conditions, as well as to the physical and chemical characteristics of the Kerkini reservoir (N Greece) and determines the trophic status. The flushing rate, and the residence time of the water show clearly the dominance of the riverine system upon the lacustrine circulation pattern. The shallowness of the reservoir, the inflow of river Strimon, and the nearly continuous functioning of the dam throughout the year should be considered as the factors influencing the circulation of the water in the reservoir. Phosphorous mean annual value, mean annual and maximum values of chlorophyll-a were found 106.6 g P 1^–1, 18.4 g 1^–1, 29.7 g 1^–1 respectively. There is a tendency of the reservoir to decline into a hypertrophic state from a eutrophic one. River Strimon contributes significantly to the overloading of the reservoir by nitrogenous agricultural effluents.