Factors controlling carbon isotope ratios of dissolved inorganic carbon in two major tributaries of the Han River,Korea

Understanding the carbon cycle of the Han River system in Korea is of prime interest in managing and preserving this valuable water resource for more than 20 million residents in the area. As a part of a comprehensive carbon cycling study for the Han River system, this report focuses on the carbon isotope compositions of dissolved inorganic carbon (DIC) in its two major tributaries, the North and the South Han Rivers. The major difference in carbonate chemistry of the tributaries originates primarily from the lithology of the catchment areas. The South Han River, draining a carbonate‐dominant terrain, has much higher alkalinities and DIC concentrations, whereas the lower concentrations in the North Han River indicate little influence of carbonate weathering. Likewise, δ¹³C_DIC values in the South Han River indicate that the DIC input from the carbonate rocks is important in controlling carbon isotope ratios of DIC. For the North Han River, the oxidation of organic material influences the amount of riverine DIC and δ¹³C_DIC values to a greater extent. Overall, remarkable seasonal and spatial variations of river chemistry and carbon isotope compositions of DIC reflect the variability in geo‐hydrologic characteristics, in the water regime, and in metabolic activities in the river water and/or the drainage areas. Copyright © 2006 John Wiley & Sons, Ltd.     

Mechanism for calcite dissolution and its contribution to development of reservoir porosity and permeability in the Kela 2 gas field,Tarim Basin,China

This study is undertaken to understand how calcite precipitation and dissolution contributes to depth-related changes in porosity and permeability of gas-bearing sandstone reservoirs in the Kela 2 gas field of the Tarim Basin, Northwestern China. Sandstone samples and pore water samples are col-lected from well KL201 in the Tarim Basin. Vertical profiles of porosity, permeability, pore water chem-istry, and the relative volume abundance of calcite/dolomite are constructed from 3600 to 4000 m below the ground surface within major oil and gas reservoir rocks. Porosity and permeability values are in-versely correlated with the calcite abundance, indicating that calcite dissolution and precipitation may be controlling porosity and permeability of the reservoir rocks. Pore water chemistry exhibits a sys-tematic variation from the Na2SO4 type at the shallow depth (3600-3630 m), to the NaHCO3 type at the intermediate depth (3630―3695 m),and to the CaCl2 type at the greater depth (3728―3938 m). The geochemical factors that control the calcite solubility include pH, temperature, pressure, Ca2 concen-tration, the total inorganic carbon concentration (ΣCO2), and the type of pore water. Thermodynamic phase equilibrium and mass conservation laws are applied to calculate the calcite saturation state as a function of a few key parameters. The model calculation illustrates that the calcite solubility is strongly dependent on the chemical composition of pore water, mainly the concentration difference between the total dissolved inorganic carbon and dissolved calcium concentration (i.e., [ΣCO2] -[Ca2 ]). In the Na2SO4 water at the shallow depth, this index is close to 0, pore water is near the calcite solubility. Calcite does not dissolve or precipitate in significant quantities. In the NaHCO3 water at the intermedi-ate depth, this index is greater than 0, and pore water is supersaturated with respect to calcite. Massive calcite precipitation was observed at this depth interval and this intensive cementation is responsible for decreased porosity and permeability. In the CaCl2 water at the greater depth, pore water is un-der-saturated with respect to calcite, resulting in dissolution of calcite cements, as consistent with microscopic dissolution features of the samples from this depth interval. Calcite dissolution results in formation of high secondary porosity and permeability, and is responsible for the superior quality of the reservoir rocks at this depth interval. These results illustrate the importance of pore water chemis-try in controlling carbonate precipitation/dissolution, which in turn controls porosity and permeability of oil and gas reservoir rocks in major sedimentary basins.     

Influence of ion exchange on dissolved load of alpine meltwaters

Meltwaters were collected in Switzerland at the border of two alpine glaciers, the Tsanfleuron glacier resting on limestones and the Tsijiore Nouve glacier flowing over gneissic rocks. Waters were analysed by atomic absorption spectrophotometry for the four major cations. Cation exchange appears to be an essential mechanism in the explanation of the dissolved cationic content of meltwaters in the frontal zone of glaciers. This is indicated by a study of the rate and characteristics of water enrichment. The rate-determining step in the process seems to be film diffusion. The influence of this diffusion is put forward in an analysis of the rates of change in concentration of the four major cations with discharge. Glacier grinding is considered as a factor favouring cation exchange in a proglacial environment.     

Solute concentrations in the lower niger river and the source rock contribution

Water quality analyses for the Niger River for the 1980/81 hydrological year are presented. The samples were collected from the main river at Lokoja, and from two main tributaries, the Kaduna and the Benue Rivers. Different water types were distinguished by the concentrations of major ions. The type Ca > Na > Mg > K - HCO₃ > SO₄ > Cl was represented at all stations during at least part of the year. Chloride was found to dominate the sulphate ion in the Kaduna and Niger, while the Benue maintained a higher concentration of sulphate relative to chloride all year round. Distinct patterns of seasonal variation in the ion concentrations were observed, particularly for the samples collected at Lokoja. Low ion concentrations were prominent during periods of high discharge, while low flow periods coincided with high dissolved ion concentrations. The contribution of rainwater to the total dissolved solids in the river waters was assessed indirectly using rainwater chemistry data from the Gulf of Guinea. The estimated rainwater contribution to the Lower Niger amounts to 5.15 mg 1^?1. Geochemical weathering calculations involving reactions of the four major minerals of granitic rocks - anorthite, biotite, albite, and K-feldspar - with carbon dioxide and water, can account for the average water composition of the Lower Niger. The proportion of the ionic components was also related to the occurrence of the respective element in the minerals.     

淮北临涣矿采煤沉陷区不同水体水化学特征及其影响因素

为研究淮北临涣矿采煤沉陷区不同水体的补给水源及溶质来源,在现场调查的基础上,系统采集丰水期、平水期、枯水期沉陷区积水、地表河水和浅层地下水样进行测试分析,采用Piper三线图、Gibbs图和因子分析方法,对不同水体水化学特征及其影响因素进行讨论.结果表明:地表水水体总溶解性固体(TDS)质量浓度表现为枯水期丰水期平水期,浅层地下水表现为枯水期平水期丰水期,地表水TDS质量浓度明显高于浅层地下水.地表水中主要阴阳离子为Na~+、Cl~-和SO_4~(2-),水化学类型主要为SO_4~(2-)-Cl~--Na~+型;浅层地下水离子以HCO_3~-、Ca~(2+)和Mg~(2+)为主,表现为HCO_3~--Ca~(2+)-Mg~(2+)型.结合Gibbs图和因子分析可知,地表水受蒸发作用、地表径流以及采煤活动等因素影响,浅层地下水在一定程度上体现出大气降水和地表水补给的特点,受岩石风化作用影响较为明显.     

Temporal variability of selected dissolved elements in the lower Orinoco River,Venezuela

Monthly analyses of pH, conductance, alkalinity, total suspended solids, dissolved major cations (Na, K, Ca and Mg), and selected dissolved trace elements (Fe, Al, Mn, Cu, Zn and Cr) were conducted on waters of the lower Orinoco River from February 2004 to May 2006. The data show strong seasonal variability. Major cations had maximum concentrations at low water, and were correlated with pH, conductance and alkalinity because of the tributaries coming from the Andean zones, where the weathering of evaporites and carbonate shales controls water chemistry. K concentrations did not show any relation with evaporite weathering, probably because large amounts of K come from the Guayana Shield rivers as a consequence of feldspar weathering. The concentrations of dissolved Fe, Mn and Cu were highest during the high water stage. Concentrations of the elements K, Cr, Zn and Cu are correlated with each other but not with dissolved Fe and Al, which probably are complexed with humic and fulvic substances. Mn concentrations did not show relationships with other variables. Inter‐annual variability of dissolved elements is explained by temporal changes in precipitation. Copyright © 2008 John Wiley & Sons, Ltd.     

Hydrogeochemistry and quality of groundwater in a part of Damodar Valley,Eastern India: an integrated geochemical and statistical approach

The influence of geochemical processes and quality of groundwater in a rural tract of Damodar Valley region were investigated. The study has distinguished the groundwater as fresh, soft to moderately hard and mainly CaHCO₃ type. The paired samples student’s t test shows the significant seasonal variations of pH, HCO₃^?, and Fe. Amphoteric exchange has lessened HCO₃^? concentration in post-monsoon which subsequently has caused to drop pH. Quite the reverse, the monsoon precipitation has triggered the additional release of Fe from iron-bearing sediments. The contaminant Cl^? is from the domestic wastewater as is evidenced by field observations. The inter-variable relations, cation and anion mechanisms, and mineral saturation indices reveal that the dissolutions of silicate and carbonate minerals are the primary sources of major ions in groundwater. The chloro-alkaline indices showed the role of ion exchange too in water chemistry. The R-mode factor analysis also successfully identified two dominant processes regulating water chemistry—geogenic sources (Ca²⁺, Mg²⁺, Na⁺, and HCO₃^?) and anthropogenic inputs (mainly Cl^?). The groundwater is found unsuitable for drinking at 82 and 93% of wells in pre- and post-monsoon seasons, respectively mainly due to elevated Fe content. The water from more than 90% of wells is appropriate for irrigation uses. The study recommends the proper treatment of contaminated water for consumption and measures to protect the groundwater from the waste water infiltration.     

The controls on boreal peatland surface water chemistry in Northern Alberta,Canada

Spatial and temporal variability in surface water chemistry, organic soil chemistry and hydrologic indicators were investigated at three poor‐fen complexes in two boreal catchments in Northern Alberta to provide insight into the dominant controls on surface water chemistry. Improved understanding of these controls is required to enable prediction of runoff chemistry in the region under changing atmospheric deposition conditions. Surface water chemistry exhibited considerable variability; within each fen conductivity, dissolved organic carbon (DOC), and Cl⁻ tended to decrease and pH tended to increase with increasing distance from the lake edge. Variations in evaporative isotopic enrichment in ²H and ¹⁸O, expressed as deuterium excess, were used to distinguish between throughflow waters and those that were more evaporatively enriched. Throughflow surface waters were more acidic primarily due to higher concentrations of DOC and NO₃⁻. Exchangeable base saturation and pH of organic soils were strongly related to surface water chemistry at two of the fen complexes, demonstrating the capacity for cation exchange to influence surface water chemistry. Fen surface water concentrations of most elements and DOC increased during the summer period (between June and August), while pH of water decreased. Evaporative concentration of the surface waters was a dominant driver, with surface water temperature increasing at both catchments. Localized groundwater discharge was an important contributor of base cations to the fens, while the organic soils are sinks for atmospherically deposited SO₄²⁻, N and Cl⁻. Copyright © 2010 John Wiley & Sons, Ltd.     

An ecological and hydrochemical study of three springs in NE Iran with the emphasis on diatom diversity

Springs are complex and taxa rich ecosystems. Diatom assemblages have received very little attention in spring ecosystems in Iran; hence, the diatom assemblage in three selected springs in northeast Iran, were investigated using multivariate analysis together with hydro chemical measures. For this purpose, water and diatom samples collected during four seasons of 2019. Hydrochemistry results revealed that water-rock interaction is the most important factor in changing the water chemistry of studied springs and their waters produced from carbonate reservoir rocks (mainly calcite). As a result, Ca-HCO₃ is predominate water type in all three springs. In this study, 75 diatom taxa identified, from which 55 were included in the analysis. Cluster analysis based on diatoms relative abundance, clustered samples in two major groups and third small group. Results of the indicator species analysis for groups and DCA analysis were in the absolute conformity. Results revealed that the diatom assemblage dominated by combination of early colonizer taxa, spring indicator taxa and cosmopolitan taxa; most of them also reported from different spring types. The results also showed that the spring’s diatom composition influence by size and morphology of the springs.     

Characterization of the groundwater flow regime and hydrochemistry of groundwater from the Buem formation,Eastern Ghana

This study demonstrates the application of multivariate statistical methods in definition of groundwater recharge and discharge areas in a sedimentary basin in Ghana. Q‐mode hierarchical cluster analysis (HCA) was applied to 57 hydrochemical data from the Buem formation in the northern part of the Volta Region in Ghana. R‐mode HCA and R‐mode factor analysis were then applied to the same dataset to reveal the processes controlling the hydrochemistry of groundwater from this hydrogeological formation. Results of both the Q‐ and R‐mode analyses were backed by graphical methods. The analyses revealed two major water types, differentiated by salinity levels into four spatial groundwater associations. The characteristics of the four groundwater types are discussed. The recharge areas are characterized by Ca? HCO₃ low salinity waters which evolve through rock–water interactions to Na? HCO₃ high salinity waters in the discharge areas. This study finds that the hydrochemistry of groundwater from this formation is mainly controlled by the weathering of minerals, principally silicates in the aquifer matrix. The effects of the chemistry of recharging precipitation are higher in the recharge areas, while mineral weathering tends to be severe close to the discharge areas in the groundwater flow regime. All the four spatial groundwater associations have low sodium content, but salinity levels increase towards the discharge areas, such that some of wells in the discharge areas may not be acceptable for irrigation on grounds of high salinities which might affect the osmotic potentials of plants. Copyright © 2011 John Wiley & Sons, Ltd.     

Mine Waters of the Eastern Donbass and Their Effect on the Chemistry of Groundwater and Surface Water in the Region

Regularities in the formation of mining water chemistry in Eastern Donbass were established and described for the 100-year period from the 1920s to 2010. The total of more than 1500 analyses were used. The changes in the chemistry were largest in the 1940s–1950s in the mines that had been recovered during World War II and after the mass abandonment of mines in the region (2002–2010). The size of groundwater resources acceptable for drinking water supply had decreased considerably; and the volumes of polluted surface water had increased abruptly. The export of dissolved substances by mining waters onto land surface reached its maximum (426 thousand t/year) in 2010. Four main lines of transformation of mine water chemistry were identified and their genesis was interpreted.     

Drought and deluge: Influence of environmental factors on water quality of kettle holes in two subsequent years with different precipitation

Thirty kettle hole ponds located in agricultural landscape of western Poland were studied with respect to physico-chemical (temperature and pH) and chemical (SC, dissolved oxygen, concentration of nutrients) variables of surface water quality during two subsequent years. Most of the ponds selected for the study host populations of endangered large branchiopod crustaceans, thus the aim of the study was to find out the rules governing these ecosystems and infer the best ways to protect them. Precipitation during the first year of the study was close to the average for the region, whereas severe drought was recorded during the second year. The influence of water regime, morphological parameters, catchment characteristics and vegetation on the parameters of water (pH, conductivity, contents of O₂, N-NH₄, N-NO₂, N-NO₃, SRP and TP) separately for both years was tested using redundancy analyses (RDA). The results showed that the factors significantly explaining the variance in water chemistry differed between years of the study. In the year of average precipitation, the most important factors were related to the morphology of the pond and its catchment. In contrast, under drought conditions the factors connected with pond vegetation and water depth were significant. However, in general, hydroperiod length of the pond was the most important factor, significant in all the models created.     

Effects of land use on water chemistry in a river draining karst terrain,southwest China

Abstract

The effects of land use on river water chemistry in a typical karst watershed (Wujiang River) of southwest China have been evaluated. Dissolved major ions and Sr isotopic compositions were determined in 11 independent sub-watersheds of the Wujiang River to investigate the spatio-temporal variations in river water chemistry and their relationship to land use. The results show significant spatial variability in pH, major ions, total dissolved solids (TDS), and Sr isotopic compositions throughout the basin. Correlation analysis indicates that nitrogen content is significantly related to forest coverage. Nitrogen and potassium generally have higher values in the rainy season, and the percentage of agricultural land controlled NO₃^- levels, which originate from anthropogenic sources. Forest cover, which varies between 35% and 71%, has no statistically significant impact on river solute concentrations, but the TDS flux is low in sub-watersheds with greater forest cover. Geological sources have a significant influence on pH and Sr isotopic compositions in river water throughout the basin.

Editor D. Koutsoyiannis

Citation Han, G., Li, F., and Tan, Q., 2014. Effects of land use on water chemistry in a river draining karst terrain, southwest China. Hydrological Sciences Journal, 59 (5), 1063–1073.     

Spatial characteristics and controlling factors of chemical weathering of loess in the dry season in the middle Loess Plateau,China

Hydrochemistry methods were used to decipher the weathering and geochemical processes controlling solute acquisition of river waters in the dry season in the middle Loess Plateau (MLP), one of the most severely eroded areas and turbid riverine systems in the world. River waters were neutral to slightly alkaline with pH varying from 7.6 to 9.6. The total dissolved solids decreased from northwest to southeast with a mean value of 804 mg/l, much higher than the global average and other large rivers in China. Ternary diagram showed that river waters were dominated by Na⁺, HCO₃^?, and Cl^? with the main water‐type of HCO₃^?–Cl^?–Na⁺. Saturation index values, Mg²⁺, Ca²⁺, and HCO₃^? analyses indicated the preferential Ca²⁺ removal by calcite precipitation. Gibbs plots and stoichiometry plots indicated that the dissolved solutes were mainly derived from rock weathering with minor anthropogenic and atmospheric inputs. Samples in the northwestern basin are also influenced by evaporation. A forward model of mass budget calculation showed that, owing to high soluble characteristics, evaporite dissolution was a major feature of river waters and contributed 41% to the total dissolved cations on average, while carbonate and silicate weathering contributed 28%,and 25% on average, respectively. Besides evaporite dissolution, cation exchange is also responsible for the high concentrations of Na⁺ in river water. Spatial variations showed that evaporite dissolution and silicate weathering were higher in the northern basin, whereas carbonate weathering was higher in the southern basin. Different from most rivers in the world, the physical erosion rates (varying from 117.7 to 4116.6 t/km²y) are much higher than the chemical weathering rates (varying from 3.54 to 6.76 t/km²y) in the MLP because of the loose structure of loess and poor vegetation in the basin. In the future, studies on comparison of water geochemistry in different seasons and on influence of different types of land use and soil salinization on water geochemistry, denudation rates, and water quality should be strengthened in the MLP. These results shed some lights on processes responsible for modern loess weathering and also indicate the importance of time‐series sampling strategy for river water chemistry. Copyright © 2016 John Wiley & Sons, Ltd.     

Water Quality Monitoring of Tropical Ponds: Location and Depth Effect in Two Case Studies

The variability in water chemistry of samples taken on a monthly basis (March 1999 to February 2000) from two shallow tropical ponds was studied. The effect of location and pond depth on water chemistry was also examined. The study demonstrated that intraannual variability in nutrient concentration is high. Thus, a high annual sampling frequency is required to provide representative annual mean water quality data. Routine monitoring during the monsoons is important for studies on dissolved oxygen and macrophyte growth. Significant differences were found between the topmost and bottommost points for samples of dissolved oxygen collected from the deepest part of both ponds. For nutrient analysis (nitrogen and phosphorus), sample from any location was found to be representative of the whole pond.     

Provenance of sandstones from the Wakino Subgroup of the Lower Cretaceous Kanmon Group, northern Kyushu, Japan

Abstract The Wakino Subgroup is a lower stratigraphic unit of the Lower Cretaceous Kanmon Group. Previous studies on provenance of Wakino sediments have mainly concentrated on either petrography of major framework grains or bulk rock geochemistry of shales. This study addresses the provenance of the Wakino sandstones by integrating the petrographic, bulk rock geochemistry, and mineral chemistry approaches. The proportions of framework grains of the Wakino sandstones suggest derivation from either a single geologically heterogeneous source terrane or multiple source areas. Major source lithologies are granitic rocks and high‐grade metamorphic rocks but notable amounts of detritus were also derived from felsic, intermediate and mafic volcanic rocks, older sedimentary rocks, and ophiolitic rocks. The heavy mineral assemblage include, in order of decreasing abundance: opaque minerals (ilmenite and magnetite with minor rutile), zircon, garnet, chromian spinel, aluminum silicate mineral (probably andalusite), rutile, epidote, tourmaline and pyroxene. Zircon morphology suggests its derivation from granitic rocks. Chemistry of chromian spinel indicates that the chromian spinel grains were derived from the ultramafic cumulate member of an ophiolite suite. Garnet and ilmenite chemistry suggests their derivation from metamorphic rocks of the epidote‐amphibolite to upper amphibolite facies though other source rocks cannot be discounted entirely. Major and trace element data for the Wakino sediments suggest their derivation from igneous and/or metamorphic rocks of felsic composition. The major element compositions suggest that the type of tectonic environment was of an active continental margin. The trace element data indicate that the sediments were derived from crustal rocks with a minor contribution from mantle‐derived rocks. The trace element data further suggest that recycled sedimentary rocks are not major contributors of detritus. It appears that the granitic and metamorphic rocks of the Precambrian Ryongnam Massif in South Korea were the major contributors of detritus to the Wakino basin. A minor but significant amount of detritus was derived from the basement rocks of the Akiyoshi and Sangun Terrane. The chromian spinel appears to have been derived from a missing terrane though the ultramafic rocks in the Ogcheon Belt cannot be discounted.     

Interbasin groundwater flow and groundwater interaction with surface water in a lowland rainforest, Costa Rica: A review

This paper reviews work related to interbasin groundwater flow (naturally occurring groundwater flow beneath watershed topographic divides) into lowland rainforest watersheds at La Selva Biological Station in Costa Rica. Chemical mixing calculations (based on dissolved chloride) have shown that up to half the water in some streams and up to 84% of the water in some riparian seeps and wells is due to high-solute interbasin groundwater flow (IGF). The contribution is even greater for major ions; IGF accounts for well over 90% of the major ions at these sites. Proportions are highly variable both among watersheds and with elevation within the same watershed (there is greater influence of IGF at lower elevations). The large proportion of IGF found in water in some riparian wetlands suggests that IGF is largely responsible for maintaining these wetlands. δ¹⁸O data support the conclusions from the major ion data. Annual water and major ion budgets for two adjacent watersheds, one affected by IGF and the other not, showed that IGF accounted for two-thirds of the water input and 92–99% of the major ion input (depending on the major ion in question) to the former watershed. The large (in some cases, dominating) influence of IGF on watershed surface water quantity and quality has important implications for stream ecology and watershed management in this lowland rainforest. Because of its high phosphorus content, IGF increases a variety of ecological variables (algal growth rates, leaf decay rate, fungal biomass, invertebrate biomass, microbial respiration rates on leaves) in streams at La Selva. The significant rates of IGF at La Selva also suggest the importance of regional (as opposed to small-scale local) water resource planning that links lowland watersheds with regional groundwater. IGF is a relatively unexplored and potentially critical factor in the conservation of lowland rainforest.     

Reactive-transport modeling of fly ash–water–brines interactions from laboratory-scale column studies

Dynamic leaching tests are important studies that provide more insights into time-dependent leaching mechanisms of any given solid waste. Hydrogeochemical modeling using PHREEQC was applied for column modeling of two ash recipes and brines generated from South African coal utility plants, Sasol and Eskom. The modeling results were part of a larger ash–brine study aimed at acquiring knowledge on (i) quantification and characterization of the products formed when ash is in contact with water–brines in different scenarios, (ii) the mineralogical changes associated with water–brine–ash interactions over time, (iii) species concentration, and (iv) leaching and transport controlling factors. The column modeling was successfully identified and quantified as important reactive mineralogical phases controlling major, minor and trace elements’ release. The pH of the solution was found to be a very important controlling factor in leaching chemistry. The highest mineralogical transformation took place in the first 10 days of ash contact with either water or brines, and within 0.1 m from the column inflow. Many of the major and trace elements Ca, Mg, Na, K, Sr, S(VI), Fe, are leached easily into water systems and their concentration fronts were high at the beginning (within 0.1 m from the column inflow and within the first 10 days) upon contact with the liquid phase. However, their concentration decreased with time until a steady state was reached. Modeling results also revealed that geochemical reactions taking place during ash–water–brine interactions does affect the porosity of the ash, whereas the leaching processes lead to increased porosity. Besides supporting experimental data, modeling results gave predictive insights on leaching of elements which may directly impact on the environment, particularly ground water. These predictions will help develop scenarios and offer potential guide for future sustainable waste management practices as a way of addressing the co-disposal of brines within inland ash dams and heaps.     

Analysis of recharge-induced geochemical change in a contaminated aquifer

Recharge events that deliver electron acceptors such as O2, NO3, SO4, and Fe3+ to anaerobic, contaminated aquifers are likely important for natural attenuation processes. However, the specific influence of recharge on (bio)geochemical processes in ground water systems is not well understood. The impact of a moderate-sized recharge event on ground water chemistry was evaluated at a shallow, sandy aquifer contaminated with waste fuels and chlorinated solvents. Multivariate statistical analyses coupled with three-dimensional visualization were used to analyze ground water chemistry data (including redox indicators, major ions, and physical parameters) to reveal associations between chemical parameters and to infer processes within the ground water plume. Factor analysis indicated that dominant chemical associations and their interpreted processes (anaerobic and aerobic microbial processes, mineral precipitation/dissolution, and temperature effects) did not change significantly after the spring recharge event of 2000. However, the relative importance of each of these processes within the plume changed. After the recharge event, the overall importance of aerobic processes increased from the fourth to the second most important factor, representing the variability within the data set. The anaerobic signatures became more complex, suggesting that zones with multiple terminal electron-accepting processes (TEAPs) likely occur in the same water mass. Three-dimensional visualization of well clusters showed that water samples with similar chemical associations occurred in distinct water masses within the aquifer. Water mass distinctions were not based on dominant TEAPs, suggesting that the recharge effects on TEAPs occurred primarily at the interface between infiltrating recharge water and the aquifer.     

Analysis of patterns of vertical and temporal distribution of phytoplankton using multifactorial analysis: Acidic Lake Caviahue, Patagonia, Argentina

Most existing studies on the algal communities of acid lakes are based on environments that have been caused by anthropogenic disturbances. Such lakes have a different origin compared to the natural acidic lakes and could be expected to differ also in the mechanisms controlling phytoplankton and trophic status. Planktonic community in Lake Caviahue is somewhat diverse in spite of the low pH of the water. Algae have a distinctive vertical distribution: the values of phytoplankton biomass remain constant throughout the water column and at times were highest in the upper end of the hypolimnion, forming a maximum or a layer of chlorophyll a at depth. The goal of this work was to investigate the factors influencing the seasonal and vertical distribution of phytoplankton. The lake was sampled between the years 2004 and 2006. Physical, chemical and biological parameters at different depths throughout the water column were determined. The interrelationships between environmental variables at different sampling dates were analyzed using an integration of multivariate matrices, multiple factor analysis, to analyze any joint partnerships in the samples. We found that phytoplankton biomass is dominated by Keratococcus rhaphidioides. With regard to zooplankton, we found a single species of rotifers (Philodina sp.). The two arms of the lake and the depths have different behaviours showing differences in the arms' conductivity, dissolved oxygen and pH. The more superficial layers were characterized by high values of phytoplankton and zooplankton biomass, organic and inorganic carbon, dissolved oxygen and pH. The deeper layers showed high values of chlorophyll a, ammonium and phosphorus (dissolved and particulate). From the multivariate analysis the relationships of the each algal species with pH, as a possible indicator of the degree of “acidophilia”, could be extracted.