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USGS1989

Petrology of the zoned calcalkaline magma chamber of Mount Mazama, Crater Lake, Oregon

Evolution of the magma chamber at Mount Mazama involved repeated recharge by two types of andesite (high-Sr and low-Sr), crystal fractionation, crystal accumulation, assimilation, and magma mixing (Bacon and Druitt 1988). This paper addresses the modal compositions, textures, mineral chemistry and magmatic temperatures of (i) products of the 6845±50 BP climactic eruption, (ii) blocks of partially fused granitoid wallrock found in the ejecta, and (iii) preclimactic rhyodacitic lavas leaked from the chamber in late Pleistocene and early Holocene time. Immediately prior to the climactic eruption the chamber contained ≳ 40 km 3 of rhyodacite (10 vol% plag + opx + aug + hb + mt + ilm, ∼880° C) overlying high-Sr andesite and cumulus-crystal mush (28–51 vol% plag + hb ± opx ± aug + mt ± ilm, 880° to ≥950° C), which in turn overlay low-Sr crystal mush (50–66 vol% plag + opx + aug ± hb ± ol + mt + ilm, 890° to ≥950† C). Despite the well known compositional gap in the ejecta, no thermal discontinuity existed in the chamber. Pre-eruptive water contents of pore liquids in most high-Sr and low-Sr mushes were 4–6 wt%, but on average the high-Sr mushes were slightly richer in water. Although parental magmas of the crystal mushes were andesitic, xenocrysts of bytownite and Ni-rich magnesian olivine in some scoriae record the one-time injection of basalt into the chamber. Textures in ol-bearing scoriae preserve evidence for the reactions ol + liq = opx and ol + aug + liq(+ plag?) = hb, which occurred in andesitic liquids at Mount Mazama. Strontium abundances in plagioclase phenocrysts constrain the petrogenesis of preclimactic and climactic rhyodacites. Phenocryst cores derived from high-Sr and low-Sr magmas have different Sr contents which can be resolved by microprobe. Partition coefficients for plagioclase in andesitic to rhyolitic glasses range from 2 to 7, and increase as glass %SiO 2 increases. Evolved Pleistocene rhyodacites (∼30–25,000 BP) and rhyodacites of the Holocene Llao Rock center (7015±45 BP) contain Sr-poor plagioclase and are derivatives from low-Sr magma. Rhyodacites of the Pleistocene Sharp Peak domes, Holocene Cleetwood flow (∼6850 BP), and climactic ejecta contain discrete Sr-rich and Sr-poor plagioclase phenocryst populations and are hybrids produced by mixing low-Sr rhyodacite (containing Sr-poor plag + opx + aug) with a more mafic high-Sr magma (with Sr-rich plag [ + hb?]). The data reinforce the conclusions of crystal-liquid mixing calculations (Bacon and Druitt 1988), and suggest some important refinements to the magma chamber model.

Oregon↗

USGS1983

Crassulacean acid metabolism in the seasonally submerged aquatic Isoetes howellii

Evidence to date is consistent with the hypothesis that the submerged aquatic Isoetes howellii Engelmann possesses crassulacean acid metabolism. Quantitative 14 C uptake studies indicate that CO 2 assimilation in both the light and dark are functions of pH and total inorganic carbon level. In both the light and dark, maximum uptake rates in 0.6 mM NaHCO 3 were double the rates in 0.3 mM NaHCO 3 . At both carbon levels there was a large drop in carbon assimilation rate between pH 6 and 8. In nature water pH and inorganic carbon level fluctuated diurnally thus complicating the determination of the contribution of light vs dark CO 2 uptake to the total carbon gain. On a sunny day between 0600 and 1200 h water chemistry changed markedly with ∼40% reduction in total carbon, ∼2 pH unit rise resulting from ∼100% depletion of free CO 2 . Under such conditions daytime deacidification in Isoetes leaves was 88% complete by noon. In contrast, on an overcast day, reduction of carbon in the water was much slower, deacidification was only 46% complete by noon and substantial malic acid levels remained in the leaves at the end of the day. Upon emergence crassulacean acid metabolism was largely lost in Isoetes leaves. Preliminary estimates suggest that under natural submerged conditions, early morning photosynthetic rates may be substantially higher than dark CO 2 uptake rates, though uptake rates throughout much of the day could be substantially lower than nightime CO 2 assimilation.

Oecologia↗

USGS1983

Crassulacean acid metabolism in Isoetes bolanderi in high elevation oligotrophic lakes

Isoetes bolanderi dominates the littoral flora of Siesta (elevation 2,440 m) and Ellery (2,905 m) lakes in the Sierra Nevada Range of California, USA. Both lakes are sparsely vegetated and I. bolanderi maintained aboveground oven dry weight of 30–50 m −22 through most of the 1981 summer growing season. Plants at the higher elevation Ellery Lake were half as large as plants at Siesta Lake and had substantially more biomass in corms. Titratable acidity levels in Isoetes leaves showed a diurnal fluctuation <50 μeq g 1 fresh weight early in the season at the highest elevation site but this increased to ∼300 μeq g 1 FW by mid-summer; starch and chlorophyll levels likewise increased in the leaves over this time. Throughout the season the magnitude of the diurnal acid change was comparable in Isoetes from both lakes but the dynamics of daytime deacidification were not. Averaged over the season, total daytime deacidification at Ellery Lake was 65% complete by noon whereas at Siesta Lake it was only 22% complete by noon. It is suggested that this may be related to the fact that Siesta Lake was more acidic and thus more carbon was in the form of free CO 2 . In both lakes water chemistry showed no consistent diurnal fluctuation in pH or free CO 2 though total inorganic carbon levels were at the extreme low end for aquatic habitats. The studies reported here suggest that under extremely low inorganic carbon levels there may be selection for nighttime CO 2 assimilation. Consistent with this hypothesis is the observation that emergent I. bolanderi plants, resulting from fluctuating water levels, initiated leaves with stomata (unlike adjacent submerged plants) and, although these leaves had substantially higher chlorophyll levels, they showed an order of magnitude less acid fluctuation than submerged leaves.

California↗

USGS1990

Acid precipitation and food quality: Inhibition of growth and survival in black ducks and mallards by dietary aluminum, calcium and phosphorus

In areas impacted by acid precipitation, water chemistry of acidic ponds and streams often changes, resulting in increased mobilization of aluminum and decreased concentration of calcium carbonate. Aluminum binds with phosphorus and inhibits its uptake by organisms. Thus, invertebrate food organisms used by waterfowl may have inadequate Ca and P or elevated Al for normal growth and development. Acid rain and its effects may be one of the factors negatively impacting American black ducks ( Anas rubripes ) in eastern North America. One-day old mallards ( A. platyrhynchos ) and black ducks were placed on one of three Ca:P regimens: low:low (LL), normal:normal (NN), and low:high (LH) with each regimen divided further into three or four Al levels for 10 weeks. Forty-five % of the black ducks died on nine different diets whereas only 28% of the mallards died on three different diets. Mortality was significantly related to diet in both species. Growth rates for body weight, culmens, wings, and tarsi of both species on control diets exceeded those on many treatment diets but the differences were less apparent for mallards than for black ducks. Differences among treatments were due to both Ca:P and A1 levels.

Archives of Environmental Contamination and Toxico↗

USGS1983

Effects of dietary ABATE® on reproductive success, duckling survival, behavior, and clinical pathology in game-farm mallards

Forty-four pairs of game-farm mallards ( Anas platyrhynchos ) were fed ABATE ® 4E (temephos) to yield 0, 1, or 10 ppm ABATE ® beginning before the initiation of lay, and terminating when ducklings were 21 days of age. The mean interval between eggs laid was greater for hens fed 10 ppm ABATE ® than for controls. Clutch size, fertility, hatchability, nest attentiveness of incubating hens, and avoidance behavior of ducklings were not significantly affected by ABATE ® ingestion. The percentage survival of ducklings to 21 days of age was significantly lower in both treated groups than in controls, but brain acetylcholinesterase (AChE) activity was not inhibited in young which died before termination of the study. In 21-day-old ducklings, aspartate aminotransferase (AST) activity increased and plasma nonspecific cholinesterase (ChE) activity was inhibited by about 20% in both treatment groups, but there were no significant differences in brain AChE or plasma alanine aminotransferase (ALT) activities, or plasma uric acid concentration. Clinical chemistry values of adults were not affected. No ABATE ® , ABATE ® sulfoxide, or ABATE ® sulfone residues were found in eggs or tissue samples.

Archives of Environmental Contamination and Toxico↗

USGS1987

Cadmium, copper, lead, and zinc determination in precipitation: A comparison of inductively coupled plasma atomic emission spectrometry and graphite furnace atomization atomic absorption spectrometry

Selected trace element analysis for cadmium, copper, lead, and zinc in precipitation samples by inductively coupled plasma atomic emission Spectrometry (ICP) and by atomic absorption spectrometry with graphite furnace atomization (AAGF) have been evaluated. This task was conducted in conjunction with a longterm study of precipitation chemistry at high altitude sites located in remote areas of the southwestern United States. Coefficients of variation and recovery values were determined for a standard reference water sample for all metals examined for both techniques. At concentration levels less than 10 micrograms per liter AAGF analyses exhibited better precision and accuracy than ICP. Both methods appear to offer the potential for cost-effective analysis of trace metal ions in precipitation. ?? 1987 Springer-Verlag.

Mikrochimica Acta↗

USGS1991

Application of electromagnetic techniques in survey of contaminated groundwater at an abandoned mine complex in southwestern Indiana, U.S.A.

In part of a large abandoned mining complex, electromagnetic geophysical surveys were used along with data derived from cores and monitoring wells to infer sources of contamination and subsurface hydrologic connections between acidic refuse deposits and adjacent undisturbed geologic materials. Electrical resistivity increases sharply along the boundary of an elevated deposit of pyritic coarse refuse, which is highly contaminated and electrically conductive, indicating poor subsurface hydrologic connections with surrounding deposits of fine refuse and undisturbed glacial material. Groundwater chemistry, as reflected in values of specific conductance, also differs markedly across the deposit's boundary, indicating that a widespread contaminant plume has not developed around the coarse refuse in more than 40 yr since the deposit was created. Most acidic drainage from the coarse refuse is by surface runoff and is concentrated around stream channels. Although most of the contaminated groundwater within the study area is concentrated within the surficial refuse deposits, transects of apparent resistivity and phase angle indicate the existence of an anomalous conductive layer at depth (>4 m) in thick alluvial sediments along the northern boundary of the mining complex. Based on knowledge of local geology, the anomaly is interpreted to represent a subsurface connection between the alluvium and a flooded abandoned underground mine. ?? 1991 Springer-Verlag New York Inc.

Environmental Geology and Water Sciences↗

USGS1989

Arsenic in ground-water under oxidizing conditions, south-west United States

Concentrations of dissolved arsenic in ground-water in alluvial basins of Arizona commonly exceed 50 μg L −1 and reach values as large as 1,300 μg L −1 . Arsenic speciation analyses show that arsenic occurs in the fully oxidized state of plus 5 (As+5), most likely in the form of HAsO4 ∼2 , under existing oxidizing and pH conditions. Arsenic in source areas presumably is oxidized to soluble As before transport into the basin or, if after transport, before burial. Probable sources of arsenic are the sulphide and arsenide deposits in the mineralized areas of the mountains surrounding the basins. Arsenic content of alluvial material ranged from 2 to 88 ppm. Occurrence and removal of arsenic in ground-water are related to the pH and the redox condition of the ground-water, the oxidation state of arsenic, and sorption or exchange. Within basins, dissolved arsenic correlates (P<0.01) with dissolved molybdenum, selenium, vanadium, and fluoride and with pH, suggesting sorption of negative ions. The sorption hypothesis is further supported by enrichment of teachable arsenic in the basin-fill sediments by about tenfold relative to the crustal abundance and by as much as a thousandfold relative to concentrations found in ground-water. Silicate hydrolysis reactions, as defined within the alluvial basins, under closed conditions cause increases in pH basinward and would promote desorption. Within the region, large concentrations of arsenic are commonly associated with the central parts of basins whose chemistries evolve under closed conditions. Arsenic does not correlate with dissolved iron (r = 0.09) but may be partly controlled by iron in the solid phase. High solid-phase arsenic contents were found in red clay beds. Large concentrations of arsenic also were found in water associated with red clay beds. Basins that contain the larger concentrations are bounded primarily by basalt and andesite, suggesting that the iron content as well as the arsenic content of the basin fill may play a role in the occurrence of arsenic in ground-water. Under oxidizing conditions in Arizona, arsenic in ground-water appears to be controlled in part by sorption or desorption of HAsO4 ∼2 on active ferric oxyhydroxide surfaces.

Arizona, California, Nevada, New Mexico↗

USGS1997

Mercury accumulation in Devils Lake, North Dakota effects of environmental variation in closed-basin lakes on mercury chronologies

Sediment cores were collected from lakes in the Devils Lake Basin in North Dakota to determine if mercury (Hg) accumulation chronologies from sediment-core data are good indicators of variations in Hg accumulation rates in saline lakes. Sediment cores from Creel Bay and Main Bay, Devils Lake were selected for detailed analysis and interpretation. The maximum Hg concentration in the Creel Bay core was 0.15 micrograms per gram at 8 to 9 centimeters. The maximum Hg concentration in the Main Bay core was 0.07 micrograms per gram at 5 to 7 centimeters. The general decreases in Hg concentrations with depth are attributed to historic variations in atmospheric Hg deposition rate. Hg stratigraphies combined with 210Pb and 137Cs dating analyses yield Hg chronologies that indicate a general increase in Hg accumulation rates in Devils Lake since the middle of the 19th century. Mean modern Hg accumulation rates in Creel Bay were 4.9 nanograms per square centimeter per year, and rates in Main Bay were 1.8 nanograms per square centimeter per year. Mean preindustrial Hg accumulation rates in Creel Bay were 1.2 nanograms per square centimeter per year, and rates in Main Bay were 1.6 nanograms per square centimeter per year. Relatively low Hg concentrations in recent sediments in the Devils Lake Basin, along with similarities in Hg accumulation rates between lakes in the Devils Lake Basin and other lakes in the northern interior of North America, indicate that local sources of Hg are not important sources of Hg. Results of the study indicate that accurate Hg chronologies are discernible in sediment cores collected from saline lakes. However, spatial and temporal variations in lake level and water chemistry common to saline lakes make interpretation of radioisotopic and geochemical chronologies difficult. Hg geochemistry in Devils Lake, and presumably in other saline lakes, is dynamic. The results of this study indicate that the absolute amount of sediment transported to Devils Lake, along with the associated Hg and total organic carbon, and the distribution of sedimentation patterns in Devils Lake may be affected by changing lake levels.

Water, Air, & Soil Pollution↗

USGS1996

Effect of whole catchment liming on the episodic acidification of two Adirondack streams

During the fall of 1989 7.7Mg/ha of calcium carbonate was applied on two tributary catchments (40 ha and 60 ha) to Woods Lake, a small (25 ha) acidic headwater lake in the western Adirondack region of New York. Stream-water chemistry in both catchment tributaries responded immediately. Acid-neutralizing capacity (ANC) increased by more than 200 μeq/L in one of the streams and more than 1000 μeq/L in the other, from pre-liming values which ranged from −25 to +40 μeq/L. The increase in ANC was primarily due to increases in dissolved Ca 2+ concentrations. Most of the initial response of the streams was due to the dissolution of calcite that fell directly into the stream channels and adjacent wetlands. A small beaver impoundment and associated wetlands were probably responsible for the greater response observed in one of the streams. After the liming of subcatchmentIV (60 ha), Ca 2+ concentrations increased with increasing stream discharge in the stream during fall rain events, suggesting a contribution from calcite dissolved within the soil and transported to the stream by surface runoff or shallow interflow. Concentrations of other ions not associated with the calcite (e.g. Na + ) decreased during fall rain events, presumably due to mixing of solute-rich base flow with more dilute shallow interflow. The strong relation between changes in Ca 2+ and changes in NO − 3 concentrations during spring snowmelt, (r 2 = 0.93, slope = 0.96, on an equivalent basis) suggests that both solutes had a common source in the organic horizon of the soil. Increases in NO − 3 concentrations during snowmelt were balanced by increases in Ca 2+ that was released either directly from the calcite or from exchange sites, mitigating episodic acidification of the stream. However, high ambient NO − 3 concentrations and relatively low ambient Ca 2+ concentrations in the stream during the spring caused the stream to become acidic despite the CaCO 3 treatment. In stream WO2 (40ha), Ca 2+ concentrations were much higher than in stream WO4 because of the dissolution of calcite which fell directly into the upstream beaver pond and its associated wetlands. Calcium concentrations decreased as both NO − 3 concentrations and stream discharge increased, due to the dilution of Ca-enriched beaver pond water by shallow interflow. Despite this dilution, Ca 2+ concentrations were high enough to more than balance strong acid anion (SO − 4 , NO − 3 , Cl − ) concentrations, resulting in a positive ANC in this stream throughout the year. These data indicate that liming of wetlands and beaver ponds is more effective than whole catchment liming in neutralizing acidic surface waters.

Biogeochemistry↗

USGS1997

The use of bulk collectors in monitoring wet deposition at high-altitude sites in winter

Concentrations of dissolved ions from samples collected by wet/dry collectors were compared to those collected by bulk collectors at Halfmoon Creek and Ned Wilson Lake in western Colorado to determine if bulk collectors can be used to monitor wet deposition chemistry in remote, high-altitude regions in winter. Hydrogen-ion concentration was significantly lower (p < 0.05) in the bulk collectors. All other ion concentrations were significantly higher (p < 0.05) in the bulk collectors except for ammonium (p > 0.05) at Halfmoon Creek. Wet deposition concentrations were predicated from bulk deposition concentrations through linear regression analysis. Results indicate that anions (chloride, nitrate and sulfate) can be predicted with a high degree of confidence. Lack of significant differences between seasonal (winter and summer) ratios of bulk to wet deposition concentrations indicates that at sites where operation of a wet/dry collector during the winter is not practical, wet deposition concentrations can be predicted from bulk collector samples through regression analysis of wet and bulk deposition data collected during the summer.

Water, Air, & Soil Pollution↗

USGS1983

Seismicity at Fuego, Pacaya, Izalco, and San Cristobal Volcanoes, Central America, 1973-1974

Seismic data collected at four volcanoes in Central America during 1973 and 1974 indicate three sources of seismicity: regional earthquakes with hypocentral distances greater than 80 km, earthquakes within 40 km of each volcano, and seismic activity originating at the volcanoes due to eruptive processes. Regional earthquakes generated by the underthrusting and subduction of the Cocos Plate beneath the Caribbean Plate are the most prominent seismic feature in Central America. Earthquakes in the vicinity of the volcanoes occur on faults that appear to be related to volcano formation. Faulting near Fuego and Pacaya volcanoes in Guatemala is more complex due to motion on a major E-W striking transform plate boundary 40 km north of the volcanoes. Volcanic activity produces different kinds of seismic signatures. Shallow tectonic or A-type events originate on nearby faults and occur both singly and in swarms. There are typically from 0 to 6 A-type events per day with b value of about 1.3. At very shallow depths beneath Pacaya, Izalco, and San Cristobal large numbers of low-frequency or B-type events are recorded with predominant frequencies between 2.5 and 4.5 Hz and with b values of 1.7 to 2.9. The relative number of B-type events appears to be related to the eruptive states of the volcanoes; the more active volcanoes have higher levels of seismicity. At Fuego Volcano, however, low-frequency events have unusually long codas and appear to be similar to tremor. High-amplitude volcanic tremor is recorded at Fuego, Pacaya, and San Cristobal during eruptive periods. Large explosion earthquakes at Fuego are well recorded at five stations and yield information on near-surface seismic wave velocities (??=3.0??0.2 km/sec.). ?? 1983 Intern. Association of Volcanology and Chemistry of the Earth's Interior.

Bulletin Volcanologique↗

USGS1980

Oxygen isotopic determinations of sequentially erupted plagioclases in the 1974 magma of Fuego Volcano, Guatemala

Plagioclases in the 1974 high-Al basalt from Fuego Volcano have ??O18 values of +6.0 to +8.5 per mil. Meteoric water cannot have played a significant role in Fuego's magma. Large, weakly zone clear phenocrysts had ??O18 values in the accepted mantle range, while patchyzoned and oscillatory-zoned plagioclases inferred to have formed later and shallower levels have slightly heavier oxygen isotopic ratios. ?? 1980 Intern. Association of Volcanology and Chemistry of the Earth's Interior.

Bulletin Volcanologique↗

USGS1980

Crystallization history of Kilauea Iki lava lake as seen in drill core recovered in 1967-1979

Kilauea Iki lava lake formed during the 1959 summit eruption, one of the most picritic eruptions of Kilauea Volcano in the twentieth century. Since 1959 the 110 to 122 m thick lake has cooled slowly, developing steadily thickening upper and lower crusts, with a lens of more molten lava in between. Recent coring dates, with maximum depths reached in the center of the lake, are: 1967 (26.5 m). 1975 (44.2 m), 1976 (46.0 m) and 1979 (52.7 m). These depths define the base of the upper crust at the time of drilling. The bulk of the core consists of a gray, olivine-phyric basalt matrix, which locally contains coarser-grained diabasic segregation veins. The most important megascopic variation in the matrix rock is its variation in olivine content. The upper 15 m of crust is very olivine-rich. Abundance and average size of olivine decrease irregularly downward to 23 m; between 23 and 40 m the rock contains 5-10% of small olivine phenocrysts. Below 40 m. olivine content and average grainsize rise sharply. Olivine contents remain high (20-45%, by volume) throughout the lower crust, except for a narrow (< 6 m) olivine depleted zone near the basalt contact. Petrographically the olivine phenocrysts in Kilauea Iki can be divided into two types. Type 1 phenocrysts are large (1-12 mm long), with irregular blocky outlines, and often contain kink bands. Type 2 crystals are relatively small (0.5-2 mm in length), euhedral and undeformed. The variations in olivine content of the matrix rock are almost entirely variations in the amount of type 1 olivines. Sharp mineral layering of any sort is rare in Kilauea Iki. However, the depth range 41-52 m is marked by the frequent occurrence of steeply dipping (70??-90??) bands or bodies of slightly vuggy olivine-rich rock locally capped with a small cupola of segregation-vein material. In thin section there is clear evidence for relative movement of melt and crystals within these structures. The segregation veins occur only in the upper crust. The most widely distributed (occurring from 4.5-59.4 m) are thin veins (most < 5 cm thick), which cut the core at moderate angles and appear to have been derived from the immediately adjacent wall-rock by filter pressing. There is also a series of thicker (0.1-1.5 m) segregation veins, which recur every 2-3 m, between 20 and 52 m. These have subhorizontal contacts and appear, from similarities in thickness and spacing, to correlate between drill holes as much as 100 m apart. These large veins are not derived from the adjacent wallrock: their mechanism of formation is still problematical. The total thickness of segregation veins in Kilauea Iki is 3-6 m in the central part of the lake, corresponding to 6-11% of the upper crust. Whole-rock compositions for Kilauea Iki fall into two groups: the matrix rock ranges from 20-7.5% MgO, while the segregation veins all contain between 6.0 and 4.5% MgO. There are no whole-rock compositions of intermediate MgO content. Samples from < 12 m show eruption-controlled chemistry. Below that depth, matrix rock compositions have higher Al2O3, TiO2 and alkalies, and lower CaO and FeO, at a given MgO content than do the eruption pumices. The probable causes of this are assimilation of low-melting components from foundered crust, plus removal of olivine, plus removal of minor augite, for rocks with MgO contents of < 8.0%. Given the observed rate of growth of the upper crust, one can infer that significant removal of the type 1 olivine phenocrysts from the upper part of the lake began in 1963 and ceased sometime prior to 1972. The process. probably gravitative settling, appears to have been inhibited earlier by gas streaming from the lower part of the lens of melt. The olivine cumulate zone, which extends into the upper crust, contains relatively few (25-40%) olivine crystals, few of which actually touch each other. The diffuseness of the cumulate zone raises the possibility that the crystals were coated with a relatively visous boundary layer

Bulletin Volcanologique↗

USGS1999

Techniques for restoration of disturbed coastal wetlands of the Great Lakes

A long history of human-induced degradation of Great Lakes wetlands has made restoration a necessity, but the practice of wetland restoration is relatively new, especially in large lake systems. Therefore, we compiled tested methods and developed additional potential methods based on scientific understanding of Great Lakes wetland ecosytems to providc an overview of approaches for restoration. We addressed this challenge by focusing on four general fields of science: hydrology, sedimentology, chemistry, and biology. Hydrologic remediation methods include restoring hydrologic connections between diked and hydrologically altered wetlands and the lakes, restoring water tables lowered by ditching, and restoring natural variation in lake levels of regulated lakes Superior and Ontario. Sedimentological remediation methods include management of sediment input from uplands, removal or proper management of dams on tributary rivers, and restoration of protective barrier beaches and sand spits. Chemical remediation methods include reducing or eliminating inputs of contaminants from point and non-pont sources, natural sediment remediation by biodegradation and chemical degradation, and active sediment remediation by removal or by in situ treatment Biological remediation methods include control of non-target organisms, enhancing populations of target organisms, and enhancing habitat for target organisms. Some of these method were used in three major restoration projects (Metzger Marsh on Lake Erie and Cootes Paradise and Oshawa Second Marsh on Lake Ontario), which are described as case studies to show practical applications of wetland restoration in the Great Lakes. Successful restoration techniques that do not require continued manipulation must be founded in the basic tenets of ecology and should mimic natural processes. Success is demonstrated by the sustainability, productivity, nutrient-retention ability, invasibility, and biotic interactions within a restored wetland.

Wetlands↗

USGS2001

Effects of stream acidification and habitat on fish populations of a North American river

Water quality, physical habitat, and fisheries at sixteen reaches in the Neversink River Basin were studied during 1991-95 to identify the effects of acidic precipitation on stream-water chemistry and on selected fish-species populations, and to test the hypothesis that the degree of stream acidification affected the spatial distribution of each fish-species population. Most sites on the East Branch Neversink were strongly to severely acidified, whereas most sites on the West Branch were minimally to moderately acidified. Mean density of fish populations ranged from 0 to 2.15 fish/m 2 ; biomass ranged from 0 to 17.5 g/m 2 . Where brook trout were present, their population density ranged from 0.04 to 1.09 fish/m 2 , biomass ranged from 0.76 to 12.2 g/m 2 , and condition (K) ranged from 0.94 to 1.07. Regression analyses revealed strong relations ( r 2 ± 0.41 to 0.99; p ≤ 0.05) between characteristics of the two most common species (brook trout and slimy sculpin) populations and mean concentrations of inorganic monomeric aluminum (Al im ), pH, Si, K + , NO 3 - , NH 4 + , DOC, Ca 2+ , and Na + ; acid neutralizing capacity (ANC); and water temperature. Stream acidification may have adversely affected fish populations at most East Branch sites, but in other parts of the Neversink River Basin these effects were masked or mitigated by other physical habitat, geochemical, and biological factors.

New York↗

USGS2023

Nitrogen-15 NMR study on the incorporation of nitrogen into aquatic NOM upon chloramination

Chloramination is being used increasingly in water treatment to lower the formation of regulated disinfection byproducts (DBPs). How monochloramine nitrogen becomes incorporated into aquatic natural organic matter (NOM) and potentially affects the formation of nitrogenous DBPs is an unresolved question in the chemistry of humic substances. To address the problem, Suwannee River NOM and Suwannee River fulvic acid were reacted with preformed 15 NH 2 Cl and analyzed by solid and liquid state 15 N NMR spectrometry. Both samples were also reacted with 15 NH 4 Cl as a control. A majority of the monochloramine nitrogen incorporated into the samples matched the structural forms resulting from the control reaction with ammonia, indicating that condensation reactions of ammonia with the carbonyl functionality can partly explain the transformation of the 15 NH 2 Cl nitrogen into the NOM. These structural forms include aminohydroquinone, 1° amide, indole, and pyridine-like nitrogens. Spectra of the samples reacted with 15 NH 2 Cl also showed possible evidence for nitrosophenol nitrogens, which would arise from the reaction of hydroxylamine or nitrite, intermediates in the chemical oxidation of the inorganic nitrogen to nitrate.

Aquatic Sciences↗

USGS2014

Geochemistry of magnetite from porphyry Cu and skarn deposits in the southwestern United States

A combination of petrographic observations, laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), and statistical data exploration was used in this study to determine compositional variations in hydrothermal and igneous magnetite from five porphyry Cu–Mo and skarn deposits in the southwestern United States, and igneous magnetite from the unmineralized, granodioritic Inner Zone Batholith, Japan. The most important overall discriminators for the minor and trace element chemistry of magnetite from the investigated porphyry and skarn deposits are Mg, Al, Ti, V, Mn, Co, Zn, and Ga—of these the elements with the highest variance for (I) igneous magnetite are Mg, Al, Ti, V, Mn, Zn, for (II) hydrothermal porphyry magnetite are Mg, Ti, V, Mn, Co, Zn, and for (III) hydrothermal skarn magnetite are Mg, Ti, Mn, Zn, and Ga. Nickel could only be detected at levels above the limit of reporting (LOR) in two igneous magnetites. Equally, Cr could only be detected in one igneous occurrence. Copper, As, Mo, Ag, Au, and Pb have been reported in magnetite by other authors but could not be detected at levels greater than their respective LORs in our samples. Comparison with the chemical signature of igneous magnetite from the barren Inner Zone Batholith, Japan, suggests that V, Mn, Co, and Ga concentrations are relatively depleted in magnetite from the porphyry and skarn deposits. Higher formation conditions in combination with distinct differences between melt and hydrothermal fluid compositions are reflected in Al, Ti, V, and Ga concentrations that are, on average, higher in igneous magnetite than in hydrothermal magnetite (including porphyry and skarn magnetite). Low Ti and V concentrations in combination with high Mn concentrations are characteristic features of magnetite from skarn deposits. High Mg concentrations (<1,000 ppm) are characteristic for magnetite from magnesian skarn and likely reflect extensive fluid/rock interaction. In porphyry deposits, hydrothermal magnetite from different vein types can be distinguished by varying Ti, V, Mn, and Zn contents. Titanium and V concentrations are highly variable among hydrothermal and igneous magnetites, but Ti concentrations above 3,560 ppm could only be detected in igneous magnetite, and V concentrations are on average lower in hydrothermal magnetite. The highest Ti concentrations are present in igneous magnetite from gabbro and monzonite. The lowest Ti concentrations were recorded in igneous magnetite from granodiorite and granodiorite breccia and largely overlap with Ti concentrations found in hydrothermal porphyry magnetite. Magnesium and Mn concentrations vary between magnetite from different skarn deposits but are generally greater than in hydrothermal magnetite from the porphyry deposits. High Mg, and low Ti and V concentrations characterize hydrothermal magnetite from magnesian skarn deposits and follow a trend that indicates that magnetite from skarn (calcic and magnesian) commonly has low Ti and V concentrations.

Arizona, New Mexico↗