BIOGEOCIIEMISTRY OF AN OLD-GROWTH FORESTED WATERSHED,OLYMPIC NATIONAL PARK,WASHINGTON1

ABSTRACT: The biogeochemistry of a coastal old-growth forested watershed in Olympic National Park, Washington, was examined. Objectives were to determine: (1) concentrations of major cations and anions and dissolved organic C (DOC) in precipitation, throughfall, stemflow, soil solution and the stream; (2) nutrient input/output budgets; and (3) nutrient retention mechanisms in the watershed. Stemilow was more acidic (pH 4.0–4.5) than throughfall (pH 5.1) and precipitation (pH 5.3). Organic acids were important contributors to acidity in throughfall and stemflow and tree species influenced pH. Soil solution pH averaged 6.2 at 40 cm depth. Stream pH was higher (7.6). Sodium (54.0 μeq L-¹) and Cl (57.6 μeq L^?1) were the dominant ions in precipitation, reflecting the close proximity to the ocean. Throughfall and stemflow were generally enriched in cations, especially K. Cation concentrations in soil solutions were generally less than those in stemilow. Ion concentrations increased in the stream. Dominant ions were Ca (759.7 μeq L^?1), Na (174.4 μeq L^?1), HCO₃ (592.0 μeq L^?1), and SO₄ (331.5 μeq L^?1) with seasonal peaks in the fall. Bedrock weathering strongly influenced stream chemistry. Highest average NO₃ concentrations were in the stream (5.2 μeq L^?1) with seasonal peaks in the fall and lowest concentrations in the growing season. Nitrogen losses were similar to inputs; annual inputs were 4.8 kg/ha (not including fixation) and stream losses were 7.1 kg/ha. Despite the age and successional status of the forest, plant uptake is an important N retention mechanism in this watershed.     

AUTUMN CHEMISTRY OF OREGON COAST RANGE STREAMS1

ABSTRACT: During an autumn runoff event we sampled 48 streams with predominantly forested watersheds and igneous bedrock in the Oregon Coast Range. The streams had acid neutralizing capacities (ANC) > 90 μeq/L and pH > 6.4. Streamwater Na ⁺, Ca^{2 +}, and Mg^{2 +} concentrations were greater than K ⁺ concentrations. Anion concentrations generally followed the order of Cl^- > NO₃^- > SO₄^2-. Chloride and Na ⁺ concentrations were highest in samples collected in streams near the Pacific Ocean and decreased markedly as distance from the coast increased. Sea salt exerted no discernible influence on stream water acid-base status during the sampling period. Nitrate concentrations in the study streams were remarkably variable, ranging from below detection to 172 μeq/L. We hypothesize that forest vegetation is the primary control of spatial variability of the NO₃^- concentrations in Oregon Coast Range streams. We believe that symbiotic N fixation by red alder in pure or mixed stands is the primary source of N to forested watersheds in the Oregon Coast Range.     

VARIATION IN ADIRONDACK,NEW YORK,LAKEWATER CHEMISTRY AS FUNCTION OF SURFACE AREA1

ABSTRACT: Data from a recent survey conducted by the Adirondack Lake Survey Corporation were used to evaluate the influence of lake surface area on the acid-base status of lakes in Adirondack State Park, New York. Acid neutralizing capacity (ANC) in the small lakes (< 4 ha) occurred more frequently at extreme values (> 200, < 0 μeq L^?1), whereas larger lakes tended to be intermediate in ANC. Consequently, acidic (ANC ≤ 0) and low-pH lakes were typically small. The small lakes also exhibited lower Ca²⁺ concentration and higher dissolved organic carbon than did larger lakes. Lakes ≥ 4 ha were only half as likely to be acidic as were lakes ≥ 1 ha in area. These data illustrate the dependence of lake chemistry on lake surface area and the importance of the lower lake area limit for a statistical survey of lake water chemistry.     

RELATIONSHIPS BETWEEN WATER QUALITY AND PHOSPHORUS CONCENTRATIONS FOR PUGET SOUND REGION LAKES1

Regression relationships were developed between summer mean total phosphorus (P) concentrations in near-surface water and both chlorophyll a concentrations and Secchi disc transparency for Puget Sound region lakes. Total P concentrations in the lakes studied ranged from 7 to 66 μ/L. The relationship between total P and chlorophyll a, based on data from 69 lakes, explained 57 percent of the variance in chlorophyll a. Predicted chlorophyll a concentrations and 95 percent confidence intervals ranged from 1 ⁺³_-0.5μg/L for 7 μg/L P to about ⁺³⁵_-10μ/L for 66 μ/L P. The relationship between total P and Secchi disc, based on data from 71 lakes, explained 53 percent of the variance in Secchi disc. Predicted Secchi disc transparencies and 95 percent confidence intervals ranged from 5.5 ^+5.5_-3.0 m for 7 μ/L P to 1.4 ^+1.5_-0.7 m for 66 μ/L P.     

The Potential Use of Synthetic Aperture Radar for Estimating Methane Ebullition From Arctic Lakes1

Abstract: Arctic lakes are significant emitters of methane (CH₄), a potent greenhouse gas, to the atmosphere; yet no rigorous quantification of the magnitude and variability of pan‐Arctic lake emissions exists. In this study, we demonstrate the potential for a new method using synthetic aperture radar (SAR) imagery to detect methane bubbles in lake ice to scale up whole‐lake measurements of CH₄ ebullition (bubbling) to regional scales. We estimated ebullition from lakes, which is often the dominant mode of lake emissions, by mapping the distribution of bubble clusters frozen in early winter ice across surfaces of seven tundra lakes and one boreal forest lake in Alaska. Applying previously measured ebullition rates associated with four distinct classes of bubble clusters found in lake ice, we estimated whole‐lake emissions from individual lakes. The percent surface area of lake ice covered with bubbles (R² = 0.68) and CH₄ ebullition rates from lakes (R² = 0.59) and were correlated with radar return values from RADARSAT‐1 Standard Beam mode 3 for the tundra lakes, suggesting that with appropriate scaling and consideration for variability in lake‐ice conditions, this technique has the potential to be used for estimating broader‐scale regional and pan‐Arctic lake methane emissions.     

Back to the basics – Estimating the sensitivity of freshwater to acidification using traditional approaches

This study examines the effects of acidifying sulphur emissions on freshwater ecosystems in the traditional territory of Treaty 8 First Nations in British Columbia (BC). Due to the absence of detailed water chemistry data for most lakes in the region, revised empirical methods for estimating freshwater sensitivity to acidification are formulated using linear regression relationships between individual chemical measurements, and critical loads of acidity calculated using the Steady State Water Chemistry (SSWC) model. Lake alkalinity is the most effective chemical indicator of acidification sensitivity in northeast BC. Critical loads of acidity (CL(A)) estimated using alkalinity range from 0.0827 to 9.48 keq ha^?1 yr^?1. Sulphur deposition estimates range from 0.0113 to 0.303 keq ha^?1 yr^?1 and do not exceed the estimated CL(A) at any of the study lakes. The spatial situation of both the lakes and the emission sources is responsible for the lack of exceedances, and expanded/continued monitoring is recommended to account for geological variability and source proliferation. Measurements of lake conductivity and alkalinity provide a means of community monitoring for freshwater acidification sensitivity as part of cumulative effects management strategies.     

CONTROL OF LAKE PHOSPHORUS WITH ALUMINUM SULFATE: DOSE DETERMINATION AND APPLICATION TECHNIQUES1

ABSTRACT: Nutrient diversion does not always bring about prompt and sufficient reduction in lake phosphorus concentration due to recycling from nutrient rich sediments. Certain lakes and reservoirs may continue to experience nuisance algal blooms and require additional restorative steps. The phosphorus precipitation/inactivation technique is a procedure to remove phosphorus from the water column and to control its release from sediments in order to achieve P-limiting conditions to algal growth. Aluminum salts have been used in advanced waste water treatment to remove phosphorus and this technology was extended to lake rehabilitation. Guidelines for dose calculation and application are generally lacking, and are provided in this report. The dose determination suggested here allows maximum application of aluminum to bottom sediments and thus emphasizes long term control of phosphorus recycling. Dose can be calculated directly from the alkalinity of the water to be treated. Titration of lake water samples of Varying alkalinity allows the establishment of the relationship between residual dissolved aluminum, alkalinity, and dose which can then be employed for lake scale applications of alum to lakes and reservoirs. Application equipment and procedures are described. These depend on site characteristics and treatment objectives and include lakeside stores, a distribution pipe, and an application barge and manifold. Alum may also be used to meet other restoration objectives including the treatment of problem flows and the reduction of particulate concentrations.     

Limitations for brine acidification due to SO2 co-injection in geologic carbon sequestration

Co-injection of sulfur dioxide during geologic carbon sequestration can cause enhanced brine acidification. The magnitude and timescale of this acidification will depend, in part, on the reactions that control acid production and on the extent and rate of SO₂ dissolution from the injected CO₂ phase. Here, brine pH changes were predicted for three possible SO₂ reactions: hydrolysis, oxidation, or disproportionation. Also, three different model scenarios were considered, including models that account for diffusion-limited release of SO₂ from the CO₂ phase. In order to predict the most extreme acidification potential, mineral buffering reactions were not modeled. Predictions were compared to the case of CO₂ alone which would cause a brine pH of 4.6 under typical pressure, temperature, and alkalinity conditions in an injection formation. In the unrealistic model scenario of SO₂ phase equilibrium between the CO₂ and brine phases, co-injection of 1% SO₂ is predicted to lead to a pH close to 1 with SO₂ oxidation or disproportionation, and close to 2 with SO₂ hydrolysis. For a scenario in which SO₂ dissolution is diffusion-limited and SO₂ is uniformly distributed in a slowly advecting brine phase, SO₂ oxidation would lead to pH values near 2.5 but not until almost 400 years after injection. In this scenario, SO₂ hydrolysis would lead to pH values only slightly less than those due to CO₂ alone. When SO₂ transport is limited by diffusion in both phases, enhanced brine acidification occurs in a zone extending only 5 m proximal to the CO₂ plume, and the effect is even less if the only possible reaction is SO₂ hydrolysis. In conclusion, the extent to which co-injected SO₂ can impact brine acidity is limited by diffusion-limited dissolution from the CO₂ phase, and may also be limited by the availability of oxidants to produce sulfuric acid.     

FATE OF NITROGEN AND PHOSPHORUS ENTERING A GULF COAST FRESHWATER LAKE: A CASE STUDY1

ABSTRACT: Nitrogen and P fluxes, transformations and water quality functions of Lake Verret (a coastal Louisiana freshwater lake), were quantified. Ortho-P, total-P, NH₄⁺-N NO₃ -N and TKN in surface water collected from streams feeding Lake Verret averaged 104, 340, 59, 185, and 1,060 mg 1^?1, respectively. Lake Verret surface water concentrations of ortho-P, total-P, NH⁺-N, NO₃^?_-N and TKN averaged 66, 191, 36, 66, and 1,292 μg 1^?1. The higher N and P concentrations were located in areas of the lake receiving drainage. Nitrification and denitrification processes were significant in removing appreciable inorganic N from the system. In situ denitrification rates determined from acetylene inhibition techniques show the lake removes 560 mg N m^?2 yr^?1. Laboratory investigations using sediment receiving 450 μg NH⁺₄-N (N-15 labeled) showed that the lake has the potential to remove up to 12.8 g N m^?2 yr^?1. Equilibrium studies of P exchanges between the sediment and water column established the potential or adsorption capacity of bottom sediment in removing P from the overlying water. Lake Verret sediment was found to adsorb P from the water column at concentrations above 50 μg P 1^?1 and the adsorption rates were as great as 300 μg P cm^?2 day^?1 Using the ¹³⁷C s dating techniques, approximately 18 g N m^?2 yr^?1 and 1.2 g P m^?2 yr^?1 were removed from the system via sedimentation. Presently elevated nutrient levels are found only in the upper reaches of the lake receiving nutrient input from runoff from streams draining adjacent agricultural areas. Nitrification, denitrification, and adsorption processes at the sediment water interface over a relatively short distance reduces the N and P levels in the water column. However, if the lake receives additional nutrient loading, elevated levels will likely cover a larger portion of the lake, further reducing water quality in the lake.     

NITROGEN TRANSFORMATIONS IN SEDIMENTS AS AFFECTED BY CHEMICAL AMENDMENTS1

ABSTRACT: A study was conducted to elucidate some of the chemical factors affecting the rate and pathways of N transformations in lake sediments. The main emphasis was placed on modifying a noncalcareous sediment with CaCO₃ to approximate the composition of a calcareous sediment. Additionally, the effects of Ca²⁺, CO₃^2-, Mg2⁺ and OH^- were evaluated by using appropriate chemicals. Further, the effect of aluminum sulfate was evaluated with both sediment types. Sediment pH at 7 days was not affected by CaCO₃, but was decreased by aluminum sulfate. The CaCO₃ treatment increased the rate of ammonification, nitrification, reduction of acetylene to ethylene and methane formation, while with few exceptions the other treatments decreased the rate of the transformations studied. Aluminum sulfate, which has been proposed as a lake restoration treatment, increased ammonification but decreased most of the other transformations.     

SENSITIVITY OF HIGH-ELEVATION STREAMS IN THE SOUTHERN BLUE RIDGE PROVINCE TO ACIDIC DEPOSITION1

ABSTRACT: The Southern Blue Ridge Province, which encompasses parts of northern Georgia, eastern Tennessee, and western North Carolina, has been predicted to be sensitive to impacts from acidic deposition, owing to the chemical composition of the bedrock geology and soils. This study confirms the predicted potential sensitivity, quantifies the level of total alkalinity and describes the chemical characteristics of 30 headwater streams of this area. Water chemistry was measured five times between April 1983 and June 1984 at first and third order reaches of each stream during baseflow conditions. Sensitivity based on total alkalinity and the Calcite Saturation Index indicates that the headwater streams of the Province are vulnerable to acidification. Total alkalinity and p11 were generally higher in third order reaches (mean, 72 μeq/θ and 6.7) than in first order reaches (64 μeq/θ and 6.4). Ionic concentrations were low, averaging 310 and 340 μeq/θ in first and third order reaches, respectively. A single sampling appears adequate for evaluating sensitivity based on total alkalinity, but large temporal variability requires multiple sampling for the detection of changes in pH and alkalinity over time. Monitoring of stream water should continue in order to detect any subtle effects of acidic deposition on these unique resource systems.     

REGIONAL CHEMISTRY OF LAKES IN MASSACHUSETTS 1

ABSTRACT: We surveyed over 2000 lakes in the State of Massachusetts (1983–1984) to examine the spatial variations in their acid-base chemistry. Our survey differed from previous surveys by including small lakes and nonpristine urban lakes. For samples collected in October 1983 and 1984, the median acid neutralizing capacity (ANC) was 184 μeq L^?1 and 5.9 percent were acidic (ANC≤O). Small lakes (<4 ha) were more likely to be acidic than large lakes. Generally, sulfate was the dominant acidifying agent, although organic anions were dominant in some of the lakes in the Cape Cod Region. The ionic composition of the lakes showed strong regional patterns which appear to be related to geology and human population density. An analysis of variance of ANC shows the six regional categories in the state explain 51 percent of the variance, while a combined general linear model of lake drainage type, color, elevation, size, silica, and hydrogen ion deposition could explain only 4.9 percent of the variation in ANC. Calcium rich, high ionic strength lakes were present in the marble bedrock in the west, and relatively dilute lakes dominated by sodium and chloride were found near the coast. Chloride concentrations were also related to population density, suggesting road salt as a likely contributing source.     

ESTIMATED BACKGROUND CONCENTRATIONS OF SULFATE IN DILUTE LAKES1

ABSTRACT: Lake water sulfate values were examined for two areas in western Norway and the western United States presently receiving low levels of sulfate in atmospheric deposition. Data from these areas were used to estimate background concentrations of sulfate in lakes found in areas currently receiving acidic deposition. The two areas contain dilute lakes with concentrations of sea-salt corrected Ca+ Mg less than 50 μeq/l or conductivity < 10μS cm^-1and receive precipitation with volume-weighted mean pH > 4.8. Based on observations from these areas, we conclude that background sulfate concentrations were probably no more than 10 to 15 μeq L^-1for areas of Norway and the U.S. containing lakes with low concentrations of base cations. For southern Norway and the northeastern U.S., present lakewater sulfate concentrations represent an increase of 7 to 10 fold above these estimated background values.     

Application of nutrient loading models to the analysis of trophic conditions in Lake Okeechobee,Florida

Lake Okeechobee (surface area = 1830 km², mean depth = 3.5 m), the largest lake in Florida, is eutrophic and has nitrogen and phosphorus loading rates in excess of nearly all established criteria. The lake is not homogeneous regarding trophic conditions, and spatial and temporal variations occur regarding nutrient limitation. Nonetheless, phosphorus loading rate and trophic state data fit reasonably well to various input-output models developed for temperate lakes. Modification of the models by regression analysis to fit data for Florida lakes resulted in improved predictions for most parameters. Analysis of nutrient management alternatives for the lake indicates that a 75% reduction of phosphorus loading from the largest source (the Taylor Creek-Nubbins Slough watershed) would reduce the average chlorophyll a concentration by less than 20%. Complete elimination of inputs from the largest nitrogen source (the Everglades Agricultural Area) would decrease the average nitrogen concentration in the lake by about 20%. Limitations of nutrient inputoutput models regarding analysis of trophic conditions and management alternatives for the lake are discussed.     

Estimating Water Budgets and Vertical Leakages for Karst Lakes in North‐Central Florida (United States) Via Hydrological Modeling1

Lin, Zhulu, 2011. Estimating Water Budgets and Vertical Leakages for Karst Lakes in North‐Central Florida (United States) Via Hydrological Modeling. Journal of the American Water Resources Association (JAWRA) 1‐16. DOI: 10.1111/j.1752‐1688.2010.00513.x Abstract: Newnans, Lochloosa, and Orange Lakes are closely hydrologically connected karst lakes located in north‐central Florida, United States. The complex karst hydrology in this region poses a great challenge to the hydrological modeling that is essential to the development of Total Maximum Daily Loads for these lakes. We used a Hydrological Simulation Program – Fortran model coupled with the parallel Parameter ESTimation model calibration and uncertainty analysis software to estimate effectively the hydrological interactions between the lakes and the underlying upper Floridan aquifer and the water budgets for these three lakes. The net results of the lake‐groundwater interactions in Newnans and Orange Lakes are that both lakes recharge the underlying upper Floridan aquifer, with the recharge rate of the latter one magnitude greater than that of the former. However, for Lochloosa Lake, the net lake‐groundwater interaction is that the lake gains water from groundwater in a significant amount, approximately 40% of its total terrestrial water input. The annual average vertical leakages estimated for Newnans, Lochloosa, and Orange Lakes are 6.0 × 10⁶, ?8.9 × 10⁶, and 44.4 × 10⁶ m³, respectively. The average vertical hydraulic conductance (K_v/b) of the units between a lake bottom and the underlying upper Floridan aquifer in this region are also estimated to be from 1.26 × 10^?4 to 1.01 × 10^?3 day^?1.     

PREDICTION OF CHLOROPHYLL A CONCENTRATIONS IN FLORIDA LAKES: THE IMPORTANCE OF PHOSPHORUS AND NITROGEN1

ABSTRACT: Models for the prediction of chlorophyll a concentrations were developed and tested using data on 223 Florida lakes. A statistical analysis showed that the best model was log (Chl a) =?2.49 + 0.269 log (TP) + 1.06 log (TN) or log (Chl a) =?2.49 + 1.06 log (TN/TP) + 1.33 log (TP) where Chl a is the chlorophyll a concentration (mg m^-3), TP is the total phosphorus concentration (mg m^-3) and TN is the total nitrogen concentration (mg m^-3). The model yields unbiased estimates of chlorophyll a concentrations over a wide range of lake types and has a 95 percent confidence interval of 29–319 percent of the calculated chlorophyll a concentrations. Other models, especially the published Dillon-Rigler and Jones-Bachmann phosphorus-chlorophyll models, are less precise when applied to Florida lakes. The data support the hypothesis that nitrogen is an important limiting nutrient in hypereutrophic lakes.     

CHANGE IN LAKE TROPHIC STATE AND INTERNAL PHOSPHORUS RELEASE AFTER ALUMINUM SULFATE APPLICATION1

ABSTRACT: Recovery of eutrophic lakes after nutrient diversion may be delayed if the lake experiences significant internal phosphorus (p) loading to the water column. A maximum dose of aluminum sulfate, defined herein, was applied to the anaerobic sediments of the hypolimnia of two dimictic Ohio lakes following septic tank diversion, with the objective of attaining long term control of the release of phosphorus to the water column from these sediments. The results were compared to a similar, downstream, untreated lake. Total phosphorus concentration declined sharply after treatment and has remained so through 1980 for both lakes, a period of 5 and 6 years of control, respectively. Internal P loading from anaerobic, hypolimnetic sediments was partially controlled by the treatment but there are other important sources, perhaps in the littoral zone, in these lakes. Algal biomass is Smaller and water transparency has increased. Both lakes became mesotrophic after treatment, as described by the Carlson (1977) trophic state index, and remain in that improved condition to date. No deleterious side effects were observed, although one lake experienced a significant decrease in diversity of planktonic microcrustacea and a lakeward extension of the macrophyte community. This method appears to be an effective and lasting means of accelerating the recovery of a eutrophic lake following nutrient diversion.     

ASPECTS OF THE UNDERWATER LIGHT FIELD OF EIGHT CENTRAL NEW YORK LAKES1

ABSTRACT: The underwater light field of eight central New York lakes, which represent a wide range of trophic state, was characterized through paired measurements of Sechi disc transparency (SD, m) and diffuse light attenuation (K_d, m^?1). A total of 90 paired measurements are included in the data base. Substantial variability in the K_d SD product with time within individual systems, and amongst systems, was observed, which indicates differences in the relative contributions of absorption and scattering to attenuation. More than 50 percent of the temporal variability in K_d was attributable to attendant variations in chlorophyll a (C, mg m^?3) in only two of the lakes. Estimates of the adsorption (a, m^?1) and scattering (b, m^?1) coefficients based on paired K_d and SD measurements compared well with more precise determinations available for one of the lakes. Determinations of a and b for the eight lakes, from SD and K_d measurements, indicated great system-specificity and temporal variability in these characteristics. The temporal variability in relative contributions of a and b to K_d is consistent with covariation of different attenuating components and the lack of correlation between C and K_d in most of the study lakes.     

EFFECTS OF FOREST HERBICIDE APPLICATIONS ON STREAMWATER CHEMISTRY IN SOUTHWESTERN BRITISH COLUMBIA1

ABSTRACT: The herbicide glyphosate was applied to portions of two watersheds in southwestern British Columbia to kill vegetation that was competing with Pseudotsuga menziesii (Douglas-fir) plantations. This application had little significant effect on streamwater chemistry (K⁺, Na²⁺, Mg²⁺, Ca²⁺, Cl^-, NOs₃^-, NH₄⁺, PO4^3-, SO₄⁼, and SiO₂ concentrations, electrical conductivity, and pH) when vegetation cover in a watershed was reduced by 4%, but had significant (P>0.05) effects, which lasted for at least five years, when cover was reduced by 43%. In this case, most parameters increased in value following the application, with K⁺ and Mg²⁺ concentrations and pH values exhibiting the most prolonged increases and NO₃^- concentrations exhibiting the greatest percentage increases. Sulphate and dissolved SiO₂ concentrations decreased following the application. Streamwater chemical fluxes showed similar trends to concentrations except that changes in fluxes were less significant and no decreases were observed. Forest management induced losses of NO₃-N in streamwater during the first five post-treatment years in the study area decreased in the order: herbicide application (approximately 40 kg/ha) < clearcutting and slashburning (approximately 20 kg/ha) < clearcutting (approximately 10 kg/ha). In watersheds similar to those of the study area, herbicide application is likely to have a greater impact on streamwater chemistry, in general, than would clearcutting or clearcutting followed by slashburning.     

COALBED METHANE PRODUCT WATER CHEMISTRY IN THREE WYOMING WATERSHEDS1

ABSTRACT: The Powder River Basin in Wyoming has become one of the most active areas of coalbed methane (CBM) development in the western United States. Extraction of methane from coalbeds requires pumping of aquifer water, which is called product water. Two to ten extraction wells are manifolded into one discharge point and product water is released into nearby unlined holding ponds. The objective of this study was to evaluate the chemistry, salinity, and sodicity of CBM product water at discharge points and associated holding ponds as a function of watershed. The product water samples from the discharge points and associated holding ponds were collected from the Cheyenne River (CHR), Belle Fourche River (BFR), and Little Powder River (LPR) watersheds during the summers of 1999 and 2000. These samples were analyzed for pH, electrical conductivity (EC), total dissolved solids (TDS), alkalinity, sodium (Na), calcium (Ca), magnesium (Mg), potassium (K), sulfate (SO₄^2‐), and chloride (C^1‐). From the chemical data, practical sodium adsorption ratio (SARp) and true sodium adsorption ratio (SARt) were calculated for the CBM discharge water and pond water. The pH, EC, TDS, alkalinity, Na, Ca, Mg, K, SARp, and SARt of CBM discharge water increased significantly moving north from the CHR watershed to the LPR watershed. CBM discharge water in associated holding ponds showed significant increases in EC, TDS, alkalinity, Na, K, SARp, and SARt moving north from the CHR to the LPR watershed. Within watersheds, the only significant change was an increase in pH from 7.21 to 8.26 between discharge points and holding ponds in the LPR watershed. However, the LPR and BFR exhibited larger changes in mean chemistry values in pH, salinity (EC, TDS), and sodicity (SAR) between CBM product water discharges and associated holding ponds than the CHR watershed. For instance, the mean EC and TDS of CBM product water in LPR increased from 1.93 to 2.09 dS/m, and froml,232 to 1,336 mg/L, respectively, between discharge and pond waters. The CHR exhibited no change in EC, TDS, Na, or SAR between discharge water and pond water. Also, while not statistically significant, mean alkalinity of CBM product water in BFR and LPR watersheds decreased from 9.81 to 8.01 meq/L and from 19.87 to 18.14 meq/L, respectively, between discharge and pond waters. The results of this study suggest that release of CBM product water onto the rangelands of BFR and LPR watersheds may precipitate calcium carbonate (CaCO₃) in soils, which in turn may decrease infiltration and increase runoff and erosion. Thus, use of CBM product water for irrigation in LPR and BFR watersheds may require careful planning based on water pH, EC, alkalinity, Na, and SAR, as well as local soil physical and chemical properties.