USGS Science⌕ Search

SEARCH · USGS Science

Results for “Nature Water”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 181 records · Page 10Linked to original sources
USGS1975

Perspective on use of fresh water for cooling systems of thermoelectric powerplants in Florida

Cooling ponds, evaporative cooling towers, and once-through cooling systems of thermoelectric powerplants consume appreciable quantities of water. In Florida a cooling pond for a 1,000 megawatt nuclear power-plant operating at full load in sulluner consumes about 12.5 million gallons of water per day (0.55 cubic metres per second). A cooling tower for a plant of the same size consumes about 14.8 million gallons per day (0.65 cubic metres per second). Because the natural water loss to evaporation is greater for a water body than for a land area of comparable size in the same general environment, the total water consumption attributable to powerplant cooling may be greater for a cooling pond than for a cooling tower in instances where, for lack of a suitable natural water body, a cooling pond is created out of a dryland area. Additional water is required to maintain the chemical quality of the recycled cooling water, the quantity varying with the chemical quality of the makeup water and the concentration of chemical constituents that can be tolerated in the cooling water. Once-through cooling systems require 5 to 10 percent less water than cooling ponds, but the total withdrawal of water for this method is so large that it is practicable in Florida only along the coast where saline water can be used. In 1970 cooling systems of powerplants in Florida consumed about 106 million gallons per day (4.6 cubic metres per second), mostly saline water. Water consumption for power production in Florida could increase to 400 million gallons per day (17.5 cubic metres per second) by 1990 and to 800 million gallons per day (35.0 cubic metres per second) by 2000. Demand also will increase greatly for other uses that require Fresh water. The continued use of saline water for cooling systems of 3owerplants would help to conserve the fresh-water supply for these uses.

Florida↗
USGS1971

Minor elements in water

A complete characterization of natural waters includes a determination of the concentrations of 30 or more minor elements. Emission spectrochemical methods are uniquely suited to the determination of a comparatively large number of minor elements, mainly those classified as heavy metals. Spectro-chemical data published by Braidech and Emory in 1935 and more recent data by Durfor and Becker, and by Barnett, Skougstad, and Miller, provide some insight into the minor-element character of the raw- and finished-water supplies of most of the major U.S. cities. Such data permit assessment of those supplies that contain either comparatively high or low concentrations of minor elements. The concentrations of many minor elements are unchanged by the municipal treatment-plant operations between the raw- and finished-water supply. On the other hand, part of the copper in a raw-water supply may be removed during treatment, even though the over-all result is a net increase in copper in the finished water. The aluminum concentration of finished water is greater than in the raw-water supply when aluminum sulfate is used as a coagulant aid. Significant amounts of iron may be removed during treatment.

Book chapter↗
USGS1958

Saline-water resources of North Dakota

Natural waters in North Dakota have been arbitrarily defined in this report as saline or fresh; water containing more than 1,000 ppm (parts per million) of dissolved solids or having a specific conductance greater than 1,400 micromhos per centimeter at 25°C is considered to be saline. A large proportion of the available water supply of North Dakota is saline.

Water Supply Paper↗
USGS2004

Estimates of natural ground-water discharge and characterization of water quality in Dry Valley, Washoe County, West-Central Nevada, 2002-2003

The Dry Valley Hydrographic Area is being considered as a potential source area for additional water supplies for the Reno-Sparks area, which is about 25 miles south of Dry Valley. Current estimates of annual ground-water recharge to Dry Valley have a considerable range. In undeveloped valleys, such as Dry Valley, long-term ground-water discharge can be assumed the same as long-term ground-water recharge. Because estimating ground-water discharge has more certainty than estimating ground-water recharge from precipitation, the U.S. Geological Survey, in cooperation with Washoe County, began a three-year study to re-evaluate the ground-water resources by estimating natural ground-water discharge and characterize ground-water quality in Dry Valley. In Dry Valley, natural ground-water discharge occurs as subsurface outflow and by ground-water evapotranspiration. The amount of subsurface outflow from the upper part of Dry Valley to Winnemucca and Honey Lake Valleys likely is small. Subsurface outflow from Dry Valley westward to Long Valley, California was estimated using Darcy's Law. Analysis of two aquifer tests show the transmissivity of poorly sorted sediments near the western side of Dry Valley is 1,200 to 1,500 square feet per day. The width of unconsolidated sediments is about 4,000 feet between exposures of tuffaceous deposits along the State line, and decreases to about 1,500 feet (0.5 mile) west of the State line. The hydraulic gradient east and west of the State line ranges from 0.003 to 0.005 foot per foot. Using these values, subsurface outflow to Long Valley is estimated to be 50 to 250 acre-feet per year. Areas of ground-water evapotranspiration were field mapped and partitioned into zones of plant cover using relations derived from Landsat imagery acquired July 8, 2002. Evapotranspiration rates for each plant-cover zone were multiplied by the corresponding area and summed to estimate annual ground-water evapotranspiration. About 640 to 790 acre-feet per year of ground water is lost to evapotranspiration in Dry Valley. Combining subsurface-outflow estimates with ground-water evapotranspiration estimates, total natural ground-water discharge from Dry Valley ranges from a minimum of about 700 acre-feet to a maximum of about 1,000 acre-feet annually. Water quality in Dry Valley generally is good and primary drinking-water standards were not exceeded in any samples collected. The secondary standard for manganese was exceeded in three ground-water samples. One spring sample and two surface-water samples exceeded the secondary standard for pH. Dry Valley has two primary types of water chemistry that are distinguishable by cation ratios and related to the two volcanic-rock units that make up much of the surrounding mountains. In addition, two secondary types of water chemistry appear to have evolved by evaporation of the primary water types. Ground water near the State line appears to be an equal mixture of the two primary water chemistries and has as an isotopic characteristic similar to evaporated surface water.

Scientific Investigations Report↗
USGS2017

At the forefront: evidence of the applicability of using environmental DNA to quantify the abundance of fish populations in natural lentic waters with additional sampling considerations

Environmental DNA (eDNA) sampling has proven to be a valuable tool for detecting species in aquatic ecosystems. Within this rapidly evolving field, a promising application is the ability to obtain quantitative estimates of relative species abundance based on eDNA concentration rather than traditionally labor-intensive methods. We investigated the relationship between eDNA concentration and Arctic char ( Salvelinus alpinus ) abundance in five well-studied natural lakes; additionally, we examined the effects of different temporal (e.g., season) and spatial (e.g., depth) scales on eDNA concentration. Concentrations of eDNA were linearly correlated with char population estimates ( = 0.78) and exponentially correlated with char densities ( = 0.96 by area; 0.82 by volume). Across lakes, eDNA concentrations were greater and more homogeneous in the water column during mixis; however, when stratified, eDNA concentrations were greater in the hypolimnion. Overall, our findings demonstrate that eDNA techniques can produce effective estimates of relative fish abundance in natural lakes. These findings can guide future studies to improve and expand eDNA methods while informing research and management using rapid and minimally invasive sampling.

Canadian Journal of Fisheries and Aquatic Sciences↗
USGS1999

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Determination of dissolved arsenic, boron, lithium, selenium, strontium, thallium, and vanadium using inductively coupled plasma-mass spectrometry

The inductively coupled plasma-mass spectrometric (ICP-MS) methods have been expanded to include the determination of dissolved arsenic, boron, lithium, selenium, strontium, thallium, and vanadium in filtered, acidified natural water. Method detection limits for these elements are now 10 to 200 times lower than by former U.S. Geological Survey (USGS) methods, thus providing lower variability at ambient concentrations. The bias and variability of the method was determined by using results from spike recoveries, standard reference materials, and validation samples. Spike recoveries at 5 to 10 times the method detection limit and 75 micrograms per liter in reagent-water, surface-water, and groundwater matrices averaged 93 percent for seven replicates, although selected elemental recoveries in a ground-water matrix with an extremely high iron sulfate concentration were negatively biased by 30 percent. Results for standard reference materials were within 1 standard deviation of the most probable value. Statistical analysis of the results from about 60 filtered, acidified natural-water samples indicated that there was no significant difference between ICP?MS and former USGS official methods of analysis.

Open-File Report↗
USGS2026

Reassessing water availability in the Nile River Basin using satellite-based irrigation water use accounting

Existing estimates of irrigation areas and water use in the Nile River Basin vary widely and are based on inconsistent data and methodologies. This study leverages advances in remote sensing to provide an up-to-date and consistent basin-wide reassessment of water use in the Nile River Basin. Land cover and actual evapotranspiration data from 2013 to 2022 were used to quantify irrigated areas, irrigation water use, and the average naturalized water yield. Across the basin, 7.1 million hectares of irrigated land consume an average of 72.5 ± 2.6 billion cubic meters (BCM) of blue water annually. Egypt and Sudan together account for 92% of the irrigated area and 97% of the irrigation water use. The basin’s average naturalized yield, evaluated at Dongola station, is determined to be between 108 and 114.4 ± 3.2 BCM. Although conservative, this updated analysis indicates the basin’s average naturalized yield is 14%–20% higher than the previous naturalized yield estimate (95 BCM) and 29%–36% higher than the commonly cited observed flow of 84 BCM, which is frequently treated as the total basin-wide available water. Importantly, the study underscores that the 84 BCM represents flow at the Aswan gauging station after upstream consumptive uses, not the total water available in the basin under naturalized conditions. This distinction is critical for accurate water accounting, planning, and governance in this water-scarce basin. This study demonstrates the value of open-source remote sensing resources in data-scarce regions while emphasizing the need for region specific validation and bias correction for improved accuracy.

Nile River Basin↗
USGS2014

Precise determination of δ 88 Sr in rocks, minerals, and waters by double-spike TIMS: A powerful tool in the study of chemical, geologic, hydrologic and biologic processes

We present strontium isotopic ( 88 Sr/ 86 Sr and 87 Sr/ 86 Sr) results obtained by 87 Sr– 84 Sr double spike thermal ionization mass-spectrometry (DS-TIMS) for several standards as well as natural water samples and mineral samples of abiogenic and biogenic origin. The detailed data reduction algorithm and a user-friendly Sr-specific stand-alone computer program used for the spike calibration and the data reduction are also presented. Accuracy and precision of our δ 88 Sr measurements, calculated as permil (‰) deviations from the NIST SRM-987 standard, were evaluated by analyzing the NASS-6 seawater standard, which yielded δ 88 Sr = 0.378 ± 0.009‰. The first DS-TIMS data for the NIST SRM-607 potassium feldspar standard and for several US Geological Survey carbonate, phosphate, and silicate standards (EN-1, MAPS-4, MAPS-5, G-3, BCR-2, and BHVO-2) are also reported. Data obtained during this work for Sr-bearing solids and natural waters show a range of δ 88 Sr values of about 2.4‰, the widest observed so far in terrestrial materials. This range is easily resolvable analytically because the demonstrated external error (±SD, standard deviation) for measured δ 88 Sr values is typically ≤0.02‰. It is shown that the “true” 87 Sr/ 86 Sr value obtained by the DS-TIMS or any other external normalization method combines radiogenic and mass-dependent mass-fractionation effects, which cannot be separated. Therefore, the “true” 87 Sr/ 86 Sr and the δ 87 Sr parameter derived from it are not useful isotope tracers. Data presented in this paper for a wide range of naturally occurring sample types demonstrate the potential of the δ 88 Sr isotope tracer in combination with the traditional radiogenic 87 Sr/ 86 Sr tracer for studying a variety of biological, hydrological, and geological processes.

Journal of Analytical Atomic Spectrometry↗
USGS2015

Methods for evaluating potential sources of chloride in surface waters and groundwaters of the conterminous United States

Chloride exists as a major ion in most natural waters, but many anthropogenic sources are increasing concentrations of chloride in many receiving waters. Although natural concentrations in continental waters can be as high as 200,000 milligrams per liter, chloride concentrations that are suitable for freshwater ecology, human consumption, and agricultural and industrial water uses commonly are on the order of 10 to 1,000 milligrams per liter. “Road salt” frequently is identified as the sole source of anthropogenic chloride, but only about 30 percent of the salt consumed and released to the environment is used for deicing. Furthermore, several studies in Southern States where the use of deicing salt is minimal also show anthropogenic chloride in rising concentrations and in strong correlation to imperviousness and road density. This is because imperviousness and road density also are strongly correlated to population density. The term “road salt” is a misnomer because deicers applied to parking lots, sidewalks, and driveways can be a substantial source of chloride in some catchments because these land covers are comparable to roadways as a percentage of the total impervious area and commonly receive higher salt application rates than some roadways. Other sources of anthropogenic chloride include wastewater, dust control on unpaved roads, fertilizer, animal waste, irrigation, aquaculture, energy production wastes, and landfill leachates. The assumption that rising chloride concentrations in surface water or groundwater is indicative of contamination by deicing chemicals rather than one or more other potential sources may preclude the identification of toxic, carcinogenic, mutagenic, or endocrine-disrupting contaminants that are associated with many sources of elevated chloride concentrations. Once the sources of anthropogenic chloride in an area of interest have been identified and measured, water and solute budgets can be estimated to guide decisionmakers to identify and apply potential mitigation measures that can reduce the problem. Scientists, engineers, regulators, and decisionmakers need information about potential sources of chloride, water and solute budgets, and methods for collecting water-quality data to help identify potential sources. This information is needed to evaluate potential sources of chloride in areas where chloride may have adverse ecological effects or may degrade water supplies used for drinking water, agriculture, or industry. Knowledge of potential sources will help decisionmakers identify the best mitigation measures to reduce the total background chloride load, thereby reducing the potential for water-quality exceedances that occur because of superposition on rising background concentrations. Also, knowledge of potential sources may help decisionmakers identify the potential for the presence of contaminants that have toxic, carcinogenic, mutagenic, or endocrine-disrupting effects at concentrations that are lower by orders of magnitude than the chloride concentrations in the source water. This report is a comprehensive synthesis of relevant information, but it is not the result of an exhaustive search for literature on each topic. The potential adverse effects of chloride on infrastructure and the environment are not discussed in this report because these issues have been extensively documented elsewhere.

Open-File Report↗
USGS2016

Trophic dynamics of shrinking Subarctic lakes: naturally eutrophic waters impart resilience to rising nutrient and major ion concentrations

Shrinking lakes were recently observed for several Arctic and Subarctic regions due to increased evaporation and permafrost degradation. Along with lake drawdown, these processes often boost aquatic chemical concentrations, potentially impacting trophic dynamics. In particular, elevated chemical levels may impact primary productivity, which may in turn influence populations of primary and secondary consumers. We examined trophic dynamics of 18 shrinking lakes of the Yukon Flats, Alaska, that had experienced pronounced increases in nutrient (>200 % total nitrogen, >100 % total phosphorus) and ion concentrations (>100 % for four major ions combined) from 1985-1989 to 2010-2012, versus 37 stable lakes with relatively little chemical change over the same period. We found that phytoplankton stocks, as indexed by chlorophyll concentrations, remained unchanged in both shrinking and stable lakes from the 1980s to 2010s. Moving up the trophic ladder, we found significant changes in invertebrate abundance across decades, including decreased abundance of five of six groups examined. However, these decadal losses in invertebrate abundance were not limited to shrinking lakes, occurring in lakes with stable surface areas as well. At the top of the food web, we observed that probabilities of lake occupancy for ten waterbird species, including adults and chicks, remained unchanged from the period 1985-1989 to 2010-2012. Overall, our study lakes displayed a high degree of resilience to multi-trophic cascades caused by rising chemical concentrations. This resilience was likely due to their naturally high fertility, such that further nutrient inputs had little impact on waters already near peak production.

Alaska↗
USGS1982

Adsorption of natural dissolved organic matter at the oxide/water interface

Natural organic matter is readily adsorbed by alumina and kaolinite in the pH range of natural waters. Adsorption occurs by complex formation between surface hydroxyls and the acidic functional groups of the organic matter. Oxides with relatively acidic surface hydroxyls, e.g. silica, do not react strongly with the organic matter. Under conditions typical for natural waters, almost complete surface coverage by adsorbed organic matter may be expected for alumina, hydrous iron oxides and the edge sites of aluminosilicates. Potentiometric titration and electrophoresis indicate that most of the acidic functional groups of the adsorbed organic matter are neutralized by protons from solution. The organic coating is expected to have a great influence on subsequent adsorption of inorganic cations and anions.

Geochimica et Cosmochimica Acta↗
USGS1995

Computational scheme for the prediction of metal ion binding by a soil fulvic acid

The dissociation and metal ion binding properties of a soil fulvic acid have been characterized. Information thus gained was used to compensate for salt and site heterogeneity effects in metal ion complexation by the fulvic acid. An earlier computational scheme has been modified by incorporating an additional step which improves the accuracy of metal ion speciation estimates. An algorithm is employed for the prediction of metal ion binding by organic acid constituents of natural waters (once the organic acid is characterized in terms of functional group identity and abundance). The approach discussed here, currently used with a spreadsheet program on a personal computer, is conceptually envisaged to be compatible with computer programs available for ion binding by inorganic ligands in natural waters.

Analytica Chimica Acta↗
USGS2013

Roles of patch characteristics, drought frequency, and restoration in long-term trends of a widespread amphibian

Despite the high profile of amphibian declines and the increasing threat of drought and fragmentation to aquatic ecosystems, few studies have examined long-term rates of change for a single species across a large geographic area. We analyzed growth in annual egg-mass counts of the Columbia spotted frog (Rana luteiventris) across the northwestern United States, an area encompassing 3 genetic clades. On the basis of data collected by multiple partners from 98 water bodies between 1991 and 2011, we used state-space and linear-regression models to measure effects of patch characteristics, frequency of summer drought, and wetland restoration on population growth. Abundance increased in the 2 clades with greatest decline history, but declined where populations are considered most secure. Population growth was negatively associated with temporary hydroperiods and landscape modification (measured by the human footprint index), but was similar in modified and natural water bodies. The effect of drought was mediated by the size of the water body: populations in large water bodies maintained positive growth despite drought, whereas drought magnified declines in small water bodies. Rapid growth in restored wetlands in areas of historical population declines provided strong evidence of successful management. Our results highlight the importance of maintaining large areas of habitat and underscore the greater vulnerability of small areas of habitat to environmental stochasticity. Similar long-term growth rates in modified and natural water bodies and rapid, positive responses to restoration suggest pond construction and other forms of management can effectively increase population growth. These tools are likely to become increasingly important to mitigate effects of increased drought expected from global climate change.

Conservation Biology↗
USGS2002

Molecular weight, polydispersity, and spectroscopic properties of aquatic humic substances

The number- and weight-averaged molecular weights of a number of aquatic fulvic acids, a commercial humic acid, and unfractionated organic matter from four natural water samples were measured by high-pressure size exclusion chromatography (HPSEC). Molecular weights determined in this manner compared favorably with those values reported in the literature. Both recent literature values and our data indicate that these substances are smaller and less polydisperse than previously believed. Moreover, the molecular weights of the organic matter from three of the four natural water samples compared favorably to the fulvic acid samples extracted from similar environments. Bulk spectroscopic properties of the fulvic substances such as molar absorptivity at 280 nm and the E4/E6 ratio were also measured. A strong correlation was observed between molar absorptivity, total aromaticity, and the weight average molecular weights of all the humic substances. This observation suggests that bulk spectroscopic properties can be used to quickly estimate the size of humic substances and their aromatic contents. Both parameters are important with respect to understanding humic substance mobility and their propensity to react with both organic and inorganic pollutants.

Environmental Science & Technology↗
USGS1964

Adsorption equilibria between earth materials and radionuclides, Cape Thompson, Alaska

The concept and the derivation of a distribution coefficient are developed. Ion exchange and the nature of competition among cations are given. Distribution coefficients for carrier-free cesium, strontium, and iodine were determined on 17 samples collected during July, 1961, in the vicinity of Cape Thompson, northwestern Alaska. High percentage uptake of these ions was measured under the test conditions. Cesium adsorption, at 1 day, was found to be represented by the mass-action equation. The distribution coefficients for cesium adsorption were so large that, in all but a few cases, very little of this nuclide would remain long in solution in the natural waters of the area. Strontium adsorption was found to be a function of the calcium-plus-magnesium concentration and to be independent of the sodium concentration. In most samples, its equilibrium is reached in less than 1 day. Iodine sorption varied with percent organic matter in the samples. If the iodine were in contact with organic matter for several days, a substantial part of it probably would be removed from solution in the natural waters.

Alaska↗
USGS1992

The aqueous photolysis of α-pinene in solution with humic acid

Terpenes are produced abundantly by environmental processes but are found in very low concentrations in natural waters. Aqueous photolysis of solutions containing α-pinene, a representative terpene, in the presence of humic acid resulted in degradation of the pinene. Comparison of this reaction to photolysis of α-pinene in the presence of methylene blue leads to the conclusion that the reactive pathway for the abiotic degradation of α-pinene is due to reaction with singlet oxygen produced by irradiation of the humic material. The initial product of single oxygen and α-pinene is a hydroperoxide. Since humic materials are prevalent in most natural waters, this mechanism of photodecomposition for α-pinene probably also applies to other terpenes in surface waters and may be reasonably considered to contribute to their low environmental concentration.

Journal of Contaminant Hydrology↗
USGS2013

New Method for Electrical Conductivity Temperature Compensation

Electrical conductivity (κ) measurements of natural waters are typically referenced to 25 °C (κ 25 ) using standard temperature compensation factors (α). For acidic waters (pH < 4), this can result in a large κ 25 error (δκ 25 ). The more the sample temperature departs from 25 °C, the larger the potential δκ 25 . For pH < 4, the hydrogen ion transport number becomes substantial and its mode of transport is different from most other ions resulting in a different α. A new method for determining α as a function of pH and temperature is presented. Samples with varying amounts of H 2 SO 4 and NaCl were used to develop the new α, which was then applied to 65 natural water samples including acid mine waters, geothermal waters, seawater, and stream waters. For each sample, the κ and pH were measured at several temperatures from 5 to 90 °C and κ 25 was calculated. The δκ 25 ranged from −11 to 9% for the new method as compared to −42 to 25% and −53 to 27% for the constant α (0.019) and ISO-7888 methods, respectively. The new method for determining α is a substantial improvement for acidic waters and performs as well as or better than the standard methods for circumneutral waters.

Environmental Science & Technology↗
USGS2019

Influenza A virus detected in native bivalves in waterfowl habitat of the Delmarva Peninsula, USA

We evaluated the prevalence of influenza A virus (IAV) in different species of bivalves inhabiting natural water bodies in waterfowl habitat along the Delmarva Peninsula and Chesapeake Bay in eastern Maryland. Bivalve tissue from clam and mussel specimens ( Macoma balthica , Macoma phenax , Mulinia sp., Rangia cuneata , Mya arenaria , Guekensia demissa , and an undetermined mussel species) from five collection sites was analyzed for the presence of type A influenza virus by qPCR targeting the matrix gene. Of the 300 tissue samples analyzed, 13 samples (4.3%) tested positive for presence of influenza virus A matrix gene. To our knowledge, this is the first report of detection of IAV in the tissue of any bivalve mollusk from a natural water body.

Delaware, Maryland, Virginia↗