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At least 343 records · Page 19Linked to original sources

Survival in pond water of four reoviruses isolated from aquatic animals

The viabilities of golden shiner virus (GSV), chum salmon virus (CSV), oyster reovirus 13P2 (13P2). and catfish reovirus (CRV) were compared following viruses incubation in pond water samples held at 4°. 20°, 25°, and 30°C for one month. At the three higher temperatures tested, viral infectivity was lost by day 15 for GSV, day 20 for CSV, and day 10 for CRV and 13P2. At 4°C. no infectious GSV was detected at day 15, while the other viruses showed little or no loss of infectivity during the 30-day incubation period. The survival of these viruses in natural waters appears to be sufficient to sustain fish-to-fish transmission.

Journal of Applied Aquaculture↗

Dissimilatory reduction of selenate and arsenate in nature

This chapter discusses the biogeochemical reduction of selenate (Se(VI)) and arsenate (As(V)) when they enter anoxic environments and are used as electron acceptors for the oxidation of organic matter. These reductions are of a dissimilative nature and support the anaerobic growth of selected bacteria which conserve energy from this process. The chapter summarizes what is known about the bacteria's taxonomy, physiology, and biochemistry. Reduction to the solid, relatively unreactive Se(0) represents a mechanism for the removal of toxic Se(VI) and Se(IV) from natural waters. The environmental ramifications of these issues are also discussed in the chapter. The number of bacterial species known to respire selenate and arsenate continues to increase. The biological reduction of selenate and arsenate occurs for a number of reasons. In general, these are assimilation, regulation of reducing equivalents, detoxification, and dissimilation. Each is discussed in detail in the chapter. The realization that arsenate and selenate are indeed suitable electron acceptors and are readily available in both natural and contaminated environments suggests that even more unrelated species will be discovered. The initial biochemical studies also suggest that there may be different pathways for selenate and arsenate reduction, with specific terminal reductases and cytochromes.

Book chapter↗

Assessment of the analytical capabilities of inductively coupled plasma-mass spectrometry

A thorough assessment of the analytical capabilities of inductively coupled plasma-mass spectrometry was conducted for selected analytes of importance in water quality applications and hydrologic research. A multielement calibration curve technique was designed to produce accurate and precise results in analysis times of approximately one minute. The suite of elements included Al, As, B, Ba, Be, Cd, Co, Cr, Cu, Hg, Li, Mn, Mo, Ni, Pb, Se, Sr, V, and Zn. The effects of sample matrix composition on the accuracy of the determinations showed that matrix elements (such as Na, Ca, Mg, and K) that may be present in natural water samples at concentration levels greater than 50 mg/L resulted in as much as a 10% suppression in ion current for analyte elements. Operational detection limits are presented.

Journal of Research of the National Bureau of Stan↗

Toxicity of synthetic musks to early life stages of the freshwater mussel Lampsilis cardium

Polycyclic musk fragrances are common additives to many consumer products. As a result of their widespread use and slow degradation rates, they are widely found in aquatic environments. This study reports on the lethal and sublethal toxicity of the polycyclic musks AHTN (Tonalide??) and HHCB (Galaxolide??) to glochidial (larval) and juvenile life stages of the freshwater mussel Lampsilis cardium (Rafinesque, 1820). In glochidia, 24-h median lethal concentrations (LC50s) ranged from 454 to 850 ??g AHTN/L and from 1000 to >1750 ??g HHCB/L (water solubility). Results for 48-h tests were similar to the 24-h tests. In 96-h tests with juveniles, we did not observe a dose-response relation between mortality and either musk. However, the growth rate was reduced by musk exposure. The median effective concentrations (EC50s, based on growth) were highly variable and ranged from 108 to 1034 ??g AHTN/L and 153 to 831 ??g HHCB/L. While all adverse effects occurred at concentrations that are much greater than those reported in natural waters (low ??g/L to ng/L), these results indicate the potential for adverse effects on these long-lived organisms from exposure to synthetic musk fragrances. ?? 2006 Springer Science+Business Media, Inc.

Archives of Environmental Contamination and Toxico↗

Glass electrode determination of sodium in closed basin waters

Because of its direct relation to total dissolved solids content, sodium concentration is the most useful single hydrochemical parameter of closed basin waters in the western United States. Therefore, it is advantageous to have a rapid method for sodium determination which could be readily adapted to field use. Accordingly, thirty waters of highly variable concentration and anionic composition from the western Great Basin have been analyzed with a sodium-sensitive glass electrode. Na + values ranged from 10 to 130,000 ppm in waters containing from 102 to 401,000 ppm total dissolved solids. The electrode values were compared with conventional sodium determinations; results differed by as much as 11 per cent, although over two-thirds were within 5 per cent. No significant relation was found between the glass electrode and conventional method differences and the total dissolved solids or sodium concentration. The comparative accuracy of electrode and conventional procedures was checked, employing solutions of known sodium concentration. It was concluded that for the analysis of sodium in natural waters the glass electrode method offers results comparable in accuracy to those obtained by conventional methods, but with increased simplicity, and therefore the possibility of rapid, accurate field measurements.

Geochimica et Cosmochimica Acta↗

Ground-water quality and discharge to Chincoteague and Sinepuxent Bays adjacent to Assateague Island National Seashore, Maryland

The U.S. Geological Survey, in cooperation with the National Park Serviceó Assateague Island National Seashore, conducted a study of the transport of nutrients in ground water in the surficial aquifer to estuaries adjacent to Assateague Island National Seashore. The study area includes Assateague Island, Chincoteague and Sinepuxent Bays, and the surface-water drainage basins of the bays. The purpose of the study was to describe ground-water-flow paths that carry freshwater to Chincoteague and Sinepuxent Bays and their tributary streams, and to collect water-quality data, particularly nutrient concentrations, associated with these fresh-water inputs. Twenty-eight ground-water monitoring wells were drilled and constructed in the surficial aquifer and underlying confining bed within the study area to collect water-level and water-quality data at various depths. Base flow was measured and water-quality samples were collected at 17 non-tidal streams within the study area during the winters of 1999 and 2000 to determine the nutrient concentrations being transported to the coastal bays from each stream. Ground-water-flow paths in the surficial aquifer are highly variable in length, ranging from less than 500 feet to longer than 5 miles. Many of the shorter flow paths end by discharging ground water as base flow to both the nontidal and tidal sections of streams, whereas longer flow paths end by discharging ground water directly to Chincoteague Bay or the Atlantic Ocean. Travel-times inferred from sulfur hexafluoride gas analyses for ground water following shorter flow paths before discharging to a stream range from less than 1 year to as long as 5 years. Ground water flowing along longer flow paths may take 30 years or more to reach the discharge point at the end of the flow path. Dissolved ammonia and dissolved nitrate are the dominant nutrients in ground water in the study area. Ammonia concentrations as high as 23.4 milligrams per liter as nitrogen were detected in anoxic ground-water samples. Nitrate concentrations in ground-water samples collected from wells ranged from below 0.05 milligram per liter as nitrogen to 15.5 milligrams per liter as nitrogen, and were highest in oxic ground water. Ammonia is less mobile in ground water than nitrate, so if it remains in the reduced state, transport to the discharge zones would be slower. Nitrate concentrations in samples of stream base flow ranged from below 0.05 milligram per liter as nitrogen to 5.28 milligrams per liter as nitrogen, and showed a significant, positive correlation with the percentage of the stream basin area used to cultivate row crops. The majority of base-flow nitrate concentrations were above 0.4 milligram per liter as nitrogen, the upper limit of the level found in natural waters in the study area, which indicates that the water quality of stream base flow at most sampled stream sites in the study area is affected by anthropogenic activities. Previous U.S. Geological Survey estimates of ground-water nitrate loads to Chincoteague and Sinepuxent Bays assumed an average stream base-flow nitrate concentration of 0.72 milligram per liter as nitrogen. The average stream base-flow nitrate concentration in samples collected during this study was 1.75 milligrams per liter as nitrogen. In addition, the presence of ammonia and organic nitrogen in stream base-flow samples may have implications for the eutrophication of the coastal bays, as these nitrogen species are available as nutrients to microorganisms and plants.

Maryland↗

Land Use and land cover and associated maps

The Geological Survey is compiling land use and land cover and associated maps for the entire United States. Land use refers to man's activities which are directly related to the land. Land cover describes the vegetation, water, natural surface, and artificial constructions at the land surface. These maps will help satisfy a longstanding need for a consistent level of detail, standardization of categories, and appropriate use of scales of compilation for a type of data frequently used by land use planners, land managers, resource management planners, and others.

General Information Product↗

Evasion of added isotopic mercury from a northern temperate lake

Isotopically enriched Hg (90% 202Hg) was added to a small lake in Ontario, Canada, at a rate equivalent to approximately threefold the annual direct atmospheric deposition rate that is typical of the northeastern United States. The Hg spike was thoroughly mixed into the epilimnion in nine separate events at two-week intervals throughout the summer growing season for three consecutive years. We measured concentrations of spike and ambient dissolved gaseous Hg (DGM) concentrations in surface water and the rate of volatilization of Hg from the lake on four separate, week-long sampling periods using floating dynamic flux chambers. The relationship between empirically measured rates of spike-Hg evasion were evaluated as functions of DGM concentration, wind velocity, and solar illumination. No individual environmental variable proved to be a strong predictor of the evasion flux. The DGM-normalized flux (expressed as the mass transfer coefficient, k) varied with wind velocity in a manner consistent with existing models of evasion of volatile solutes from natural waters but was higher than model estimates at low wind velocity. The empirical data were used to construct a description of evasion flux as a function of total dissolved Hg, wind, and solar illumination. That model was then applied to data for three summers for the experiment to generate estimates of Hg re-emission from the lake surface to the atmosphere. Based on ratios of spike Hg to ambient Hg in DGM and dissolved total Hg pools, ratios of DGM to total Hg in spike and ambient Hg pools, and flux estimates of spike and ambient Hg, we concluded that the added Hg spike was chemically indistinguishable from the ambient Hg in its behavior. Approximately 45% of Hg added to the lake over the summer was lost via volatilization.

Ontario↗

Reactions of metal ions at surfaces of hydrous iron oxide

Cu, Ag and Cr concentrations in natural water may be lowered by mild chemical reduction involving ferric hydroxide-ferrous ion redox processes. V and Mo solubilities may be controlled by precipitation of ferrous vanadate or molybdate. Concentrations as low as 10 −8.00 or 10 −9.00 M are readily attainable for all these metals in oxygen-depleted systems that are relatively rich in Fe. Deposition of manganese oxides such as Mn 3 O 4 can be catalyzed in oxygenated water by coupling to ferrous-ferric redox reactions. Once formed, these oxides may disproportionate, giving Mn 4+ oxides. This reaction produces strongly oxidizing conditions at manganese oxide surfaces. The solubility of As is significantly influenced by ferric iron only at low pH. Spinel structures such as chromite or ferrites of Cu, Ni, and Zn, are very stable and if locally developed on ferric hydroxide surfaces could bring about solubilities much below 10 −9.00 M for divalent metals near neutral pH. Solubilities calculated from thermodynamic data are shown graphically and compared with observed concentrations in some natural systems.

Geochimica et Cosmochimica Acta↗

Chemical composition of snow in the northern Sierra Nevada and other areas

Melting snow provides a large part of the water used throughout the western conterminous United States for agriculture, industry, and domestic supply. It is an active agent in chemical weathering, supplies moisture for forest growth, and sustains fish and wildlife. Despite its importance, virtually nothing has been known of the chemical character of snow in the western mountains until the present study. Analysis of more than 100 samples, most from the northern Sierra Nevada, but some from Utah, Denver, Colo., and scattered points, shows that melted snow is a dilute solution containing measurable amounts of some or all of the inorganic constituents commonly found in natural water. There are significant regional differences in chemical composition; the progressive increase in calcium content with increasing distance eastward from the west slope of the Sierra Nevada is the most pronounced. The chemical character of individual snowfalls is variable. Some show predominant influence of oceanic salt; others show strong effects of mineralization from continental sources, probably largely dust. Silica and boron were found in about half the samples analyzed for these constituents; precipitation is seldom analyzed for these substances. Results of the chemical analyses for major constituents in snow samples are summarized in the following table. The median and mean values for individual constituents are derived from 41-78 samples of Sierra Nevada snow, 6-18 samples of Utah snow, and 6-17 samples of Denver, Colo., snow. The sodium, chloride, and perhaps boron found in snow are probably incorporated in moisture-laden air masses as they move over the Pacific Ocean. Silica, although abundant in the silicate-mineral nuclei found in some snowflakes, may be derived in soluble form largely from dust. Calcium, magnesium, and some bicarbonate are probably added by dust of continental origin. The sources of the other constituents remain unknown. When snowmelt comes in contact with the lithosphere, the earlier diversity of chemical type largely disappears. The melt water rapidly increases its content of dissolved solids and becomes calcium magnesium bicarbonate in type. Silica, whose concentration increases more than tenfold, shows the largest gain; calcium and bicarbonate contents also increase markedly. Most of the additional mineral matter is from soft and weathered rock; bicarbonate, however, is largely from the soil atmosphere. Investigators, some reporting as much as a century ago, concentrated attention largely on nitrogen compounds and seldom reported other constituents except chloride and sulfate. The Northern European precipitation-sampling network provides the most comprehensive collection of data on precipitation chemistry, but it does not segregate snow from other forms of precipitation. The present study establishes with confidence the chemical character of snow in the Sierra Nevada, and suggests that the dissolved-solids content of precipitation increases with increasing distance inland from the Pacific Coast.

Arizona, California, Colorado, Nevada, Oregon, Uta↗

The Solubility and Stabilization of Ikaite (CaCO3·6H2O) from 0° to 25°C: Environmental and Paleoclimatic Implications for Thinolite Tufa

We determined the solubility of ikaite from 0° to 25°C to model its saturation state in natural waters and test the hypothesis that it is the precursor of the calcite pseudomorphs in thinolite tufa of Quaternary Lake Lahontan. Reversible solubility at buffered $P_{CO_{2}}$ yields the following expression for the dissolution constant of ikaite: $log K_{ikaite} = 0.15981 - 2011.1/T$. Where $T = ^{\circ}K$, and $0^{\circ}C \leq t \leq 25^{\circ}C$. Derived standard state properties are $\Delta G_{ikaite}^{\circ} = -2541.9 kJmol^{-1} \pm 0.66; \Delta H_{ikaite}^{\circ} = -2973.4 kJmol^{-1} \pm 1.02; S_{ikaite}^{\circ} = 306.6 JT^{-1}mol^{-1} \pm 1.2$. Modeling shows that ikaite is undersaturated at all temperatures in seawater and in alkaline lakes, but that it rapidly approaches saturation near 0°C. Its precipitation in near-freezing marine sediments requires large additions of $HCO_{3}$ to pore fluids from the diagenetic decomposition of organic matter. Its crystallization in tufas of alkaline lakes, however, requires only small additions of Ca from springs. Simple kinetic experiments show that ikaite is stabilized in natural environments by orthophosphate, which prevents the crystallization of the more stable anhydrous forms of $CaCO_{3}$ but does not interact with the ikaite. Therefore, the presence of ikaite or its pseudomorphs is an indicator of near-freezing conditions in environments with high concentrations of orthophosphate. If ikaite is the precursor of thinolite tufa, then the thinolite likely grew below the sediment-water interface at the site of sublacustrine springs during prolonged cold periods.

Journal of Geology↗

Effects of the earthquake of March 27, 1964, at Anchorage, Alaska

Anchorage, Alaska’s largest city, is about 80 miles west-northwest of the epicenter of the March 27 earthquake. Because of its size, Anchorage bore the brunt of property damage from the quake; it sustained greater losses than all the rest of Alaska combined. Damage was caused by direct seismic vibration, by ground cracks, and by landslides. Direct seismic vibration affected chiefly multistory buildings and buildings having large floor areas, probably because of the long period and large amplitude of the seismic waves reaching Anchorage. Most small buildings were spared. Ground cracks caused capricious damage throughout the Anchorage Lowland. Cracking was most prevalent near the heads or within landslides but was also widespread elsewhere. Landslides themselves caused the most devastating damage. Triggering of landslides by the earthquake was related to the physical-engineering properties of the Bootlegger Cove Clay, a glacial estuarine-marine deposit that underlies much of the Anchorage area. The Bootlegger Cove Clay contains zones of low shear strength, high water content, and high sensitivity that failed under the vibratory stress of the earthquake. Shear strength in sensitive zones ranged from less than 0.2 tsf to about 0.5 tsf; sensitivity ranged from about 10 to more than 40. Sensitive zones generally are centered about 10 to 20 feet above sea level, between zones of stiff insensitive clay. Many physical tests by the U.S. Army Corps of Engineers were directed toward analyzing the causes of failure in the Bootlegger Cove Clay and finding possible remedies. Strengths and sensitivities were measured directly in the field by means of vane shear apparatus. A4tterberg limits, natural water contents, triaxial shear, sensitivity, dynamic modulus, consolidation strength, and other properties were measured in the laboratory. Pulsating-load tests simulated earthquake loading. Most of the destructive landslides in the Anchorage area moved primarily by translation rather than by rotation. Thus, all the highly damaging slides were of a single structural dynamic family despite wide variations in size, appearance, and complexity. They slid on nearly horizontal slip surfaces after loss of strength in the Bootlegger Core Clay. Same failures are attributed to spontaneous liquefaction of sand layers. All translatory slides surmounted flat-topped bluffs bounded marginally by steep slopes facing lower ground. Destructive translatory slides occurred in the downtown area (Fourth Avenue slide and L Street slide), at Government Hill, and at Turnagain Heights. Less destructive slides occurred in many other places-mostly uninhabited or undeveloped areas. In most translatory slides, damage was greatest in graben areas at the head and in pressure-ridge areas at the toe. Many buildings inside the perimeters of slide blocks were little damaged despite horizontal translations of several feet. The large Turnagain Heights slide, however, was characterized by a complete disintegration and drastic lowering of the prequake land surface. Extensive damage back from the slide, moreover, was caused by countless tension cracks. An approximation of the depth of failure in the Bootlegger Cove Clay in the various slides may be obtained by using a geometric relationship herein called the "graben rule." Because the cross-sectional area of the graben at the head of the slide approximated the cross-sectional area of the space voided behind the slide block as the block moved outward, the depth of failure was equal to the area of the graben divided by the lateral displacement. This approximation supplements and accords with test data obtained from borings. The graben rule should apply to any translatory slide in which flowage of material from the zone of failure has not been excessive. Geologic evidence indicates that landslides similar to those triggered by the March 27 earthquake have occurred in the Anchorage area at various times in the past.

Alaska↗

Double-disk solid-phase extraction--Simultaneous cleanup and trace enrichment of herbicides and metabolites from environmental samples

Phenylurea and triazine herbicides, including some metabolites, were isolated from water and soil extracts by solid-phase extraction using a layered system of two extraction disks, a method called double-disk solid-phase extraction. The first disk consisted of strong anion exchange (SAX) of 10-μm styrene divinylbenzene (SDB) particles embedded in Teflon, and the second disk was a C 18 disk of 10-μm particles also embedded in Teflon. A volume of 500 mL of water or aqueous soil extract is passed through the layered system with the SAX disk first. The purpose of the SAX disk is to remove the humic and fulvic acids from the water or aqueous soil extract by ion exchange through their carboxyl groups. Even during methanol elution of herbicides, the humic substances remain bound to the SAX disk with >85% retention. Elution with methanol results in more than 90% recovery of the herbicides from the layered extraction disks. Removal of the humic and fulvic acids results in greater sensitivity for diode array detection quantitation (0.05 μg/L for herbicides) by substantially reducing the absorbance of the humic peak on the LC chromatogram. The herbicides adsorb to the SAX disk either through hydrogen bonding to the anion-exchange sites or by hydrophobic interaction with the SDB surface of the anion-exchange disk. The method was tested for the analysis of natural water samples from the Mississippi Embayment, a cotton-growing area of the southeastern United States.

Analytical Chemistry↗

Evaluation of methods used from 1965 through 1982 to determine inorganic constituents in water samples

Since 1962, the U.S. Geological Survey has prepared and distributed Standard Reference Water Samples (SRWS) to participating laboratories in order to alert them to possible analytical deficiencies. This report marks the first time that a concentrated effort has been made to examine and compare the SRWS data for each constituent by the analytical method that was used to obtain the data. Unlike laboratories that participate in interlaboratory studies that are designed to determine the precision and accuracy of a particular analytical method, laboratories that participate in the SRWS program are allowed to select the method used to analyze a reference sample and are requested to report the method used. Data for a particular method could not be compared with a 'true' value because the data were obtained from analyses of reference samples that were prepared using natural waters; however, where possible a comparison was made between the mean concentrations obtained by the various analytical methods that were used to determine each constituent. Where enough information is available, models for predicting the precisions of the methods have been developed, and the precisions have been compared. In addition to the data presented in the reports, this evaluation provides a good indication of methods that were used routinely to analyze water samples during the 18 years of study.

Water Supply Paper↗

Constraints on the utility of MnO 2 cartridge method for the extraction of radionuclides: A case study using 234 Th

[1] Large volume (10 2 -10 3 L) seawater samples are routinely processed to investigate the partitioning of particle reactive radionuclides and Ra between solution and size-fractionated suspended particulate matter. One of the most frequently used methods to preconcentrate these nuclides from such large volumes involves extraction onto three filter cartridges (a prefilter for particulate species and two MnO 2 -coated filters for dissolved species) connected in series. This method assumes that the extraction efficiency is uniform for both MnO 2 -coated cartridges, that no dissolved species are removed by the prefilter, and that any adsorbed radionuclides are not desorbed from the MnO 2 -coated cartridges during filtration. In this study, we utilized 234 Th-spiked coastal seawater and deionized water to address the removal of dissolved Th onto prefilters and MnO 2 -coated filter cartridges. Experimental results provide the first data that indicate (1) a small fraction of dissolved Th (<6%) can be removed by the prefilter cartridge; (2) a small fraction of dissolved Th (<5%) retained by the MnO 2 surface can also be desorbed, which undermines the assumption of uniform extraction efficiency for Th; and (3) the absolute and relative extraction efficiencies can vary widely. These experiments provide insight on the variability of the extraction efficiency of MnO 2 -coated filter cartridges by comparing the relative and absolute efficiencies and recommend the use of a constant efficiency on the combined activity from two filter cartridges connected in series for future studies of dissolved 234 Th and other radionuclides in natural waters using sequential filtration/extraction methods. ?? 2009 by the American Geophysical Union.

Geochemistry, Geophysics, Geosystems↗

Relations of Tualatin River water temperatures to natural and human-caused factors

Aquatic research has long shown that the survival of cold-water fish, such as salmon and trout, decreases markedly as water temperatures increase above a critical threshold, particularly during sensitive life stages of the fish. In an effort to improve the overall health of aquatic ecosystems, the State of Oregon in 1996 adopted a maximum water-temperature standard of 17.8 degrees Celsius (68 degrees Fahrenheit), based on a 7-day moving average of daily maximum temperatures, for most water bodies in the State. Anthropogenic activities are not permitted to raise the temperature of a water body above this level. In the Tualatin River, a tributary of the Willamette River located in northwestern Oregon, water temperatures periodically surpass this threshold during the low-flow summer and fall months.An investigation by the U.S. Geological Survey quantified existing seasonal, diel, and spatial patterns of water temperatures in the main stem of the river, assessed the relation of water temperatures to natural climatic conditions and anthropogenic factors (such as wastewater-treatment-plant effluent and modification of riparian shading), and assessed the impact of various flow management practices on stream temperatures. Half-hourly temperature measurements were recorded at 13 monitoring sites from river mile (RM) 63.9 to RM 3.4 from May to November of 1994. Four synoptic water- temperature surveys also were conducted in the upstream and downstream vicinities of two wastewater-treatment-plant outfalls. Temperature and streamflow time-series data were used to calibrate two dynamic-flow heat-transfer models, DAFLOW-BLTM (RM 63.9-38.4) and CE-QUAL-W2 (RM 38.4-3.4). Simulations from the models provided a basis for approximating 'natural' historical temperature patterns, performing effluent and riparian-shading sensitivity analyses, and evaluating mitigation management scenarios under 1994 climatic conditions. Findings from the investigation included (1) under 'natural' conditions the temperature of the river would exceed the State standard of 17.8 degrees Celsius at many locations during the low-flow season, (2) current operation of wastewater-treatment plants increases the temperature of the river downstream of the plants under low-flow conditions, (3) river temperature is significantly affected by riparian shade variations along both the tributaries and the main stem, (4) flow releases during the low-flow season from the Henry Hagg Lake reservoir decrease the river temperature in the upper section, and (5) removal of a low diversion dam at RM 3.4 would slightly decrease temperatures below RM 10.0.

Oregon↗

Legacy sediment as a potential source of orthophosphate: Preliminary conceptual and geochemical models for the Susquehanna River, Chesapeake Bay watershed, USA

Nutrient pollution from agriculture and urban areas plus acid mine drainage (AMD) from legacy coal mines are primary causes of water-quality impairment in the Susquehanna River, which is the predominant source of freshwater and nutrients entering the Chesapeake Bay. Recent increases in the delivery of dissolved orthophosphate (PO 4 ) from the river to the bay may be linked to long-term increases in pH, decreased acidity of precipitation, and decreased acidity, iron, and aluminum loading from widespread AMD. Since the 1950s, baseline pH increased from ~6.5 to ~8 in the West Branch and “North Branch” of the Susquehanna River, which drain bituminous and anthracite coalfields of Pennsylvania. A current baseline pH of ~8 and daily maxima exceeding 9 have been documented along the lower Susquehanna River. In response to improved river quality, bioavailable PO 4 now may be released into solution from legacy sediment that has filled major impoundments in lower reaches of the river. At typical pH (5–8) of natural water, aqueous PO 4 species tend to be adsorbed by hydrous iron, aluminum, and manganese oxides that coat soil and sediment particles; however, PO 4 may be substantially desorbed at pH >8. We created a geochemical model that simulates equilibrium aqueous/solid distributions of PO 4 as pH and other solution characteristics change. Considering current conditions in the lower Susquehanna River, the model demonstrates potential for extensive release of adsorbed PO 4 at pH >8. Empirical data from laboratory experiments corroborate model results. The transfer of PO 4 into the water column may increase algae growth, which removes CO 2 and drives pH to higher values, facilitating additional PO 4 release and exacerbating the potential for harmful algal blooms. Thus, legacy sediment is a currently unquantified source of PO 4 that warrants consideration by resource managers and programs collaborating to reduce phosphorus loads to the bay and similar settings worldwide.

Chesapeake Bay watershed↗

A comparison of high-resolution specific conductance-based end-member mixing analysis and a graphical method for baseflow separation of four streams in hydrologically challenging agricultural watersheds

Quantifying the relative contributions of different sources of water to a stream hydrograph is important for understanding the hydrology and water quality dynamics of a given watershed. To compare the performance of two methods of hydrograph separation, a graphical program [baseflow index (BFI)] and an end-member mixing analysis that used high-resolution specific conductance measurements (SC-EMMA) were used to estimate daily and average long-term slowflow additions of water to four small, primarily agricultural streams with different dominant sources of water (natural groundwater, overland flow, subsurface drain outflow, and groundwater from irrigation). Because the result of hydrograph separation by SC-EMMA is strongly related to the choice of slowflow and fastflow end-member values, a sensitivity analysis was conducted based on the various approaches reported in the literature to inform the selection of end-members. There were substantial discrepancies among the BFI and SC-EMMA, and neither method produced reasonable results for all four streams. Streams that had a small difference in the SC of slowflow compared with fastflow or did not have a monotonic relationship between streamflow and stream SC posed a challenge to the SC-EMMA method. The utility of the graphical BFI program was limited in the stream that had only gradual changes in streamflow. The results of this comparison suggest that the two methods may be quantifying different sources of water. Even though both methods are easy to apply, they should be applied with consideration of the streamflow and/or SC characteristics of a stream, especially where anthropogenic water sources (irrigation and subsurface drainage) are present.

Hydrological Processes↗