CHEMICAL COMPOSITION OF SOFTWATER FLORIDA LAKES AND THEIR SENSITIVITY TO ACID PRECIPITATION1

ABSTRACT: Based on alkalinity data for 596 lakes, 31 percent of Florida's 7300 lakes have < 100 μeq/l alkalinity and are sensitive to acid depostion. More than two-thirds of the lakes in 12 northern Florida counties fit this criterion. Increasing aluminum and decreasing nutrient and chlorophyll a concentrations were observed with decressing pH in a survery of 20 softwater lakes. Maximum measured aluminum values (100-150 μg/L) are below levels asociated with fish toxicity. Factor analysis showed that lake chemistry was related to three principal factors, representing three major processes: watershed weathering, acidification, and nutrient inputs. An acidification index defined as the difference between excess SO₄^2- and excess (Ca²⁺+Mg²⁺) accounted for 74 percent of the variance in lake pH. Comparison of historical (late 1950a) and present data for pH, alkalinity, and excess SO₄^2- indicated loss of alkalinity (>25 μeq/L) and increase in excess SO₄^2- (16-34 μeq/L) in several softwater lakes.     

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.     

Model Calculations of Total Maximum Daily Loads of Mercury for Drainage Lakes1

Abstract: The Watershed Analysis Risk Management Framework watershed model was enhanced to simulate the transport and fate of mercury and to calculate the fish mercury concentrations (FMC) attained by fish through the food web. The model was applied to Western Lake Superior Basin of Minnesota, which has many peat lands and lakes. Topographic, land use, and soil data were used to set up the model. Meteorology and precipitation chemistry data from nearby monitoring stations were compiled to drive the model. Simulated flow and mercury concentrations for several stream stations were comparable to available data. The model was used to perform mercury total maximum daily load calculations for two contrasting drainage lakes (Wild Rice Lake and Whiteface Reservoir). The model results for wet deposition, dry deposition, evasion, watershed yield, and soil sequestration of mercury were comparable with available actual data. The model predicted lake ice cover from November to April and weak stratification in summer, typical of shallow lakes in cold regions. The simulated sulfate decrease and methylmercury increase near the lake bottom in late summer are caused by sulfate reduction and mercury methylation that occur in the surficial sediment. Simulated FMC were within the range of observed values and the R² of correlation between the simulated and observed FMC was 0.77. Under the 1989‐2004 base condition, the average simulated FMC of four‐year‐old walleye was 0.31 μg/g for Whiteface Reservoir and 0.15 μg/g for Wild Rice Lake. The FMC criterion in Minnesota is 0.2 μg/g. Wild Rice Lake already meets this criterion without any load reduction. The model showed that a 65% reduction in atmospheric mercury deposition will not, by itself, allow Whiteface Reservoir to meet the criterion in 15 years. Additional best management practices will be needed to reduce 50% of the watershed input.     

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.     

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.     

STREAM CHEMISTRY IN THE SOUTHERN BLUE RIDGE: FEASIBILITY OF A REGIONAL SYNOPTIC SAMPLING APPROACH1

ABSTRACT: A pilot study, which was conducted in the Southern Blue Ridge geographical province of the Southeastern U.S., demonstrated the feasibility of a probability-based regional synoptic design for the National Stream Survey, which is a project aimed at estimating the number and percentage of streams in various regions of the U.S. that are acidic or at risk from acid deposition. Estimated population distributions for key chemical variables were not appreciably affected by week-to-week variability in stream chemistry during the spring index period chosen for the study. Differences were observed in estimated acid neutralizing capacity (ANC), nitrate, and pH frequency distributions between spring and summer. Observations made at the downstream node did not represent the chemistry of the entire reach for some variables (ANC and nitrate) as indicated by differences in chemical concentrations between upstream and downstream sampling locations. Coefficients of variation in chemical species were low enough to provide a reasonably stable classification of streams based on ANC. Although median ANC, sulfate, and nitrate concentrations were quite low in the region, the probability of finding streams with ph < 6.3 is less than 1.3 percent at the α= 0.05 confidence level.     

ACID PRECIPITATION AND WEATHERING BY ORGANIC ACIDS IN LABRAI)OR LAKE BASINS1

ABSTRACT: Thirty-five lakes in southern Labrador sampled in 1981 were resampled in 1989 and water chemistry values were compared between visits. Results showed higher pH, specific conductance, acid neutralization capacity, color, and base cations values in 1989, though sulfate, the ion most likely to reflect acid precipitation impacts, did not vary. The major ion changes measured were probably due to natural hydrological variations and not to changes in acid inputs. Results from the 1989 data showed a slight, but significant, decrease in water sulfate concentration trend from western to eastern Labrador, though most values, even in the western portion of the study area, fell close to the values considered “background” by Brakke et at. (1989). Base cation concentrations exceeded those which could be predicted from weathering by carbonic and bicarbonic acid. Assuming that little weathering is generated by acid precipitation in this region, the excess cations measured are probably a result of bedrock dissolution from organic acids generated by plant decomposition. Calculations showed that organic acid effect could be responsible for 9 to 52 percent of total weathering in the study basins.     

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.     

OCCURRENCE OF TOTAL DISSOLVED PHOSPHORUS IN UNCONSOLIDATED AQUIFERS AND AQUITARDS IN IOWA1

ABSTRACT: Seven sets of ground water samples from 103 observation wells were analyzed for total dissolved phosphorus (TDP) in four areas and five materials including loess and loess derived alluvium in the Deep Loess Hills of western Iowa, outwash and fractured till adjacent to Clear Lake in north central Iowa, fractured till in central Iowa, and a sand and gravel aquifer in northwest Iowa. Land use in ground water recharge zones in all four areas is dominated by crop or animal production or both. Concentrations of TDP exceeding the minimum laboratory detection limit of 20 μg/l as P were found in all areas and in all materials sampled. Samples from the outwash deposits associated with Clear Lake contained significantly larger concentrations than all other areas and materials with a median of 160 μg/l. Water from fractured till in three areas produced the smallest range of concentrations with a median of 40 μg/l. The mean value of TDP in all sample sets exceeded 50 μg/l, an important ecological threshold that causes increased productivity in lakes and perennial streams and one being considered as a surface water nutrient standard by regulatory agencies. These results clearly show that ground water in essentially all near‐surface aquifers and aquitards discharging to Iowa's streams and lakes is capable of sustaining P concentrations of 50 to 100 μg/l in streams, lakes, and reservoirs. Consequently, even if point discharges and sediment sources of P are substantially reduced, ground‐water discharge to surface water may exceed critical thresholds under most conditions.     

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.     

ENVIRONMENTAL AUDITING: Exceedance of Critical Loads for Lakes in Finland,Norway, and Sweden: Reduction Requirements for Acidifying Nitrogen and Sulfur Deposition

/ The main objectives of this study were to identify the regions inFennoscandia where the critical loads of sulfur (S) and acidifying nitrogen(N) for lakes are exceeded and to investigate the consequences for depositionreductions, with special emphasis on the possible trade-offs between S and Ndeposition in order to achieve nonexceedance. In the steady-state model forcalculating critical loads and their exceedances, all relevant processesacting assinks for N and S are considered. The critical loads of N and S areinterrelated (defining the so-called critical load function), and therefore asingle critical load for one pollutant cannot be defined without makingassumptions about the other. Comparing the present N and S deposition withthe critical load function for each lake allows determination of thepercentage of lakes in the different regions of Fennoscandia where: (1) Sreductions alone can achieve nonexceedance, (2) N reductions alone aresufficient, and (3) both N and S reductions are required but to a certaindegree interchangeable. Secondly, deposition reduction requirements wereassessed by fixing the N deposition to the present level, in this wayanalyzing the reductions required for S, and by computing the percentage oflakes exceeded in Finland, Norway and Sweden for every possible percentdeposition reduction in S and N, in this way showing the (relative)effectiveness of reducing S and/or N deposition. The results showed clearregional patterns in the S and N reduction requirements. In practically thewhole of Finland and the northern parts of Scandinavia man-made acidificationof surface waters could be avoided by reducing S deposition alone. In thesouthern parts of Sweden some reductions in N deposition are clearly neededin addition to those for S. In southern Norway strong reductions are requiredfor both N and S deposition.KEY WORDS: Acidification; Critical load; Exceedance; Sulfur; Nitrogen;Deposition; Lake     

Simulated effects of sulfur deposition on nutrient cycling in class I wilderness areas

We predicted the effects of sulfate (SO(4)) deposition on wilderness areas designated as Class I air quality areas in western North Carolina using a nutrient cycling model (NuCM). We used three S deposition simulations: current, 50% decrease, and 100% increase. We measured vegetation, forest floor, and root biomass and collected soil, soil solution, and stream water samples for chemical analyses. We used the closest climate stations and atmospheric deposition stations to parameterize NuCM. The areas were: Joyce Kilmer (JK), Shining Rock (SR), and Linville Gorge (LG). They differ in soil acidity and nutrients, and soil solution and stream chemistry. Shining Rock and LG have lower soil solution base cation and higher acidic ion concentrations than JK. For SR and LG, the soil solution Ca/Al molar ratios are currently 0.3 in the rooting zone (A horizon), indicating Al toxicity. At SR, the simulated Ca/Al ratio increased to slightly above 1.5 after the 30-yr simulation regardless of S deposition reduction. At LG, Ca/Al ratios ranged from 1.6 to 2.4 toward the end of the simulation period, the 100% increase scenario had the lower value. Low Ca/Al ratios suggest that forests at SR and LG are significantly stressed under current conditions. Our results also suggest that SO(4) retention is low, perhaps contributing to their high degree of acidification. Their soils are acidic, low in weatherable minerals, and even with large reductions in SO(4) and associated acid deposition, it may take decades before these systems recover from depletion of exchangeable Ca, Mg, and K.     

ARE RURAL RESIDENTS WILLING TO PAY ENOUGH TO IMPROVE DRINKING WATER QUALITY?1

ABSTRACT: The concentrations of iron and sulfate in community water supplies are a concern for a number of areas in southwestern Minnesota. This study used the contingent valuation method to determine how much consumers would be willing to pay to improve their drinking water quality. On average, individuals were willing to pay US$5.25 per month (in 1995 U.S. dollars) to reduce the level of iron and US$4.33 per month to reduce the level of sulfate in their water to the USEPA's secondary standards for drinking water quality. Respondents with negative perceptions of their drinking water quality were willing to pay more to improve water quality. The aggregate annual willingness to pay (WTP) for all consumers in community water systems in southwestern Minnesota that were out of compliance with water quality standards were estimated to be US$2.4 million and US$2.0 million (in 1995 dollars) for reducing the levels of iron and sulfate, respectively. Yet the total WTP of consumers who use small community water systems may not be enough to pay the full cost of providing improved water in those systems. Economies of scale in water treatment and difficulties in financing improvements mean that technical innovation, government assistance, or institutional changes may be needed to improve water quality in these areas.     

Natural alkalinity generation in neutral lakes affected by acid mine drainage

Lakes in surface mining areas are often subject to continuous loads of acid mine drainage. The knowledge of internal alkalinity generation in a lake is necessary to predict if the lake will stay circumneutral or may acidify. The most important processes of alkalinity production in lakes are sulfate reduction, denitrification, and the burial of N in the sediment. By summarizing data from the literature, we present probable rates of these different processes in circumneutral mining lakes. The critical acidity load that can probably be compensated for by internal processes, is 5.09 mmol(-) m(-2) d(-1) in productive lakes and 0.50 mmol(-) m(-2) d(-1) in less productive lakes. Under the assumption that methanogenesis is inhibited by high sulfate concentrations, the highest probable acidity loads in such lakes are 6.85 mmol(-) m(-2) d(-1) and 1.06 mmol(-) m(-2) d(-1), respectively. Denitrification, sulfate reduction, and N burial contributed significantly to total alkalinity production. Sulfate reduction had the largest potential. However, existing models cannot predict alkalinity generation from sulfate concentrations alone because the long-term stability of reduced S compounds in the sediment is crucial for a sustainable biological alkalinity generation. The larger acid-neutralizing potential of higher trophic lakes is caused both by higher rates of microbial activity and by a greater stability of reduced reaction products in the sediment. The largest uncertainties in our knowledge with respect to the total alkalinity budget are related to microbial processes in sulfate-rich freshwater lakes and the long-term stability of reduced reaction products in the sediment.     

Health benefits due to reductions of CO levels

A method is presented by which an upper limit of the adverse health effect of existing ambient CO concentrations on the U. S. population can be estimated. The method is based upon estimating the primary human physiological response to CO concentrations (COHb%) for the population in terms of person-hour-COHb>1.5% resulting from the time exposure of the population to CO concentrations in excess of the federally designated ambient air quality standard. The estimates of person-hour-COHb>1.5% are for exposures only to ambient CO concentrations and do not take into account the additional CO exposure for people who smoke or have occupational exposures.We estimate that there were up to 30.9×10⁹ person-hour-COHb>1.5% in 1973 due to ambient concentrations in excess of the ambient 8-hour CO standard, with approximately 5×10⁹ person-hour-COHb>1.5% occurring West of the Continental Divide and 25.9>10⁹ person-hour-COHb>1.5% occuring East of the Continental Divide; of these 21.3×10⁹ personhour-COHb>1.5% occurred in New York City. It was also estimated that a 60% reduction in 1973 ambient concentrations of CO (corresponding to an automotive emmision standard of less than 15 g/mile) would be needed to reduce to zero the person-hour-COHb>1.5%. The maximum estimated effects on the U.S. population of increases in ambient CO concentration above 1973 levels are also presented.     

Tracing sources of sulfur in the Florida Everglades

We examined concentrations and sulfur isotopic ratios (34S/32S, expressed as delta34S in parts per thousand [/1000] units) of sulfate in surface water, ground water, and rain water from sites throughout the northern Everglades to establish the sources of sulfur to the ecosystem. The geochemistry of sulfur is of particular interest in the Everglades because of its link, through processes mediated by sulfate-reducing bacteria, to the production of toxic methylmercury in this wetland ecosystem. Methylmercury, a neurotoxin that is bioaccumulated, has been found in high concentrations in freshwater fish from the Everglades, and poses a potential threat to fish-eating wildlife and to human health through fish consumption. Results show that surface water in large portions of the Everglades is heavily contaminated with sulfate, with the highest concentrations observed in canals and marsh areas receiving canal discharge. Spatial patterns in the range of concentrations and delta34S values of sulfate in surface water indicate that the major source of sulfate in sulfur-contaminated marshes is water from canals draining the Everglades Agricultural Area. Shallow ground water underlying the Everglades and rain water samples had much lower sulfate concentrations and delta34S values distinct from those found in surface water. The delta34S results implicate agricultural fertilizer as a major contributor to the sulfate contaminating the Everglades, but ground water under the Everglades Agricultural Area (EAA) may also be a contributing source. The contamination of the northern Everglades with sulfate from canal discharge may be a key factor in controlling the distribution and extent of methylmercury production in the Everglades.     

FOG AND ACIDIFICATION IMPACTS ON ION BUDGETS OF BASINS IN NOVA SCOTIA,CANADA1

ABSTRACT: We examined hydrogeochemical records for a dozen watersheds in and near Kejimkujik National Park in southwestern Nova Scotia by relating stream ion concentrations and fluxes to atmospheric deposition, stream type (lake inlet versus outlet; brown versus clear water), and watershed type (catchment area, topography, soils, and dominant forest cover type). We found that fog and dry deposition make important contributions to S, N, Cl, H, Ca, Mg, K, and Na inputs into these watersheds. Seasalt chloride deposition from rain, snow, fog, and dry deposition equal total stream outputs on a region‐wide basis. Chloride outputs, however, differ among watersheds by a factor of about two, likely due to local differences in air flow and vegetational fog interception. We found that most of the incoming N is absorbed by the vegetation, as stream water NO3^‐ and NH4⁺ are very low. Our results also show that the vegetation and the soils absorb about half of the incoming SO4². In comparison with other North American watersheds with similar forest vegetation, Ca outputs are low, while Mg and K outputs are similar to other regions. Soil exchangeable Ca and soil cation exchange capacity are also very low. We found that first‐order forest streams with no upstream lakes have a distinct seasonal pattern that neither corresponds with the seasonal pattern of atmospheric deposition, nor with the seasonal pattern of downstream lake outlets.     

Mobilization and Toxicity Potential of Aluminum from Alum Floc Deposits in Kensico Reservoir,New York

There is detailed literature on the mobilization of aluminum (Al) from soil to surface waters as a result of elevated acidic deposition to base‐poor forest watersheds. There is considerably less information on the mobilization and effects of Al from the application of alum that is used in some water supplies to control turbidity during high‐flow events. We report on the results of field measurements, laboratory sediment release experiments, and chemical equilibrium calculations conducted to evaluate the potential for the mobilization of Al from alum floc deposits in sediments of Kensico Reservoir, New York. Under ambient water quality conditions, mobilization of sediment Al is not a noteworthy concern at Kensico Reservoir. However, under experimental conditions of low pH, low acid neutralizing capacity (ANC), and low temperature, the inorganic fraction of monomeric Al can be mobilized from Kensico sediments to concentrations that would likely impair the health of aquatic organisms (>2 μmol/l). Elevated concentrations of monomeric Al were observed only when ANC decreased below 50 μeq/l, which is outside the range of values observed in Kensico during the 1997‐2007 interval (120‐460 μeq/l). Concentrations of complexing ligands are relatively low in Kensico waters (i.e., fluoride, naturally occurring organic solutes) and do not appear to substantially contribute to potential Al mobilization. For other water supplies with low ANC, the potential for sediment release of Al may exist.     

Contaminants of Emerging Concern in Fish from Western U.S. and Alaskan National Parks — Spatial Distribution and Health Thresholds

Remote national parks of the western U.S. and Alaska are not immune to contaminants of emerging concern. Semivolatile organic compounds (SOCs) such as pesticides and PCBs can selectively deposit from the atmosphere at higher rates in cold, high‐elevation and high‐latitude sites, potentially increasing risk to these ecosystems. In the environment, SOCs magnify up food chains and are known to increase health risks such as cancer and reproductive impairment. One hundred twenty‐eight fish in 8 national parks in Alaska and the western U.S. were analyzed for contaminant concentrations, assessed by region, and compared to human and wildlife health thresholds. SOC concentrations from an additional 133 fish from a previous study were also included, for a total of 31 water bodies sampled. PCBs, endosulfan sulfate, and p,p′‐DDE were among the most frequently detected contaminants. Concentrations of historic‐use pesticides dieldrin, p,p′‐DDE, and/or chlordanes in fish exceeded USEPA guidelines for human subsistence fish consumers and wildlife (kingfisher) health thresholds at 13 of 14 parks. Average concentrations in fish ranged from 0.6‐280 ng/g lipid (0.02‐7.3 μg/g ww). Contaminant loading was highest in fish from Alaskan and Sierra Nevada parks. Historic compounds were highest in Alaskan parks, while current‐use pesticides were higher in the Rockies and Sierra Nevada. This study provides a rigorous analysis of CECs in fish from national parks and identifies regions at potential risk.