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At least 379 records · Page 21Linked to original sources
USGS1991

Major-ion and selected trace-metal chemistry of the Biscayne Aquifer, Southeast Florida

The major-ion and selected trace-metal chemistry of the Biscayne aquifer was characterized as part of the Florida Ground-Water Quality Monitoring Network Program, a multiagency cooperative effort concerned with delineating baseline water quality for major aquifer systems in the State. The Biscayne aquifer is unconfined and serves as the sole source of drinking water for more than 3 million people in southeast Florida. The Biscayne aquifer consists of highly permeable interbedded limestone and sandstone of Pleistocene and Pliocene age underlying most of Dade and Broward Counties and parts of Palm Beach and Monroe Counties. The high permeability is largely caused by extensive carbonate dissolution. Water sampled from 189 wells tapping the Biscayne aquifer was predominantly a calcium bicarbonate type with some mixed types occurring in coastal areas and near major canals. Major - ion is areally uniform throughout the aquifer. According to nonparametric statistical tests of major ions and dissolved solids, the concentrations of calcium, sodium, bicarbonate, and dissolved solids increased significantly with well depth ( 0.05 significance level ), probably a result of less circulation at depth. Potassium and nitrate concentrations decreased significantly with depth. Although the source of recharge to the aquifer varies seasonally, there was no statistical difference in the concentration of major ions in pared water samples from 27 shallow wells collected during wet and dry seasons. Median concentrations for barium, chromium, copper, lead, and manganese were below maximum or secondary maximum contaminant levels set by the US Environmental Protection Agency. The median iron concentration only slightly exceeded the secondary maximum contaminant level. The concentration of barium was significantly related (0.05 significance level) to calcium and bicarbonate concentration. No distinct areal pattern or vertical distribution of the selected trace metals was evident in water from the Biscayne aquifer. Sources for trace metals found in water from the Biscayne aquifer may include local contamination, well-construction techniques, canal - aquifer interactions, and natural occurrence in area soils and rock.

Florida↗
USGS1993

Water quality, organic chemistry of sediment, and biological conditions of streams near an abandoned wood-preserving plant site at Jackson, Tennessee

An investigation of water quality, organic sediment chemistry, and biological conditions of streams near an abandoned wood-preserving plant site at Jackson, Tennessee, was conducted during December 1990. The study was designed to assess the extent of possible contamination of water and biota in the streams from creosote-related discharge originating at this Superfund site. Central Creek, adjacent to the plant, had degraded water quality and biological conditions. Water samples from the most downstream station on Central Creek contained 30 micrograms per liter of pentachlorophenol, which exceeds the State's criterion maximum concentrations of 9 micrograms per liter for fish and aquatic life. Bottom-sediment samples from stations on Central Creek contained concentrations of acenaphthene, napthalene, and phenanthrene ranging from 1,400 to 2,500 micrograms per kilogram. Chronic or acute toxicity resulted during laboratory experiments using test organisms exposed to creosote-related contaminants. Sediment elutriate samples from Central Creek caused slightly to highly toxic effects on Ceriodaphnia dubia. Pimephales promelas, and Photobacterium phosphoreum. Fish-tissue samples from this station contained concentrations of naphthalene. dibenzofuran, fluorene, and phenanthrene ranging from 1.5 to 3.9 micrograms per kilogram Blue-green algae at this station represented about 79 percent of the organisms counted, whereas diatoms accounted for only 11 percent. Benthic invertebrate and fish samples from Central Creek had low diversity and density. Sediment samples from a station on the South Fork Forked Deer River downstream from its confluence with Central Creek contained concentrations of acenaphthene, anthracene, chrysene, fluoranthene, fluorene, pyrere, and phenanthrene ranging from 2,800 to 69,000 micrograms per kilogram. Sediment elutriate samples using water as elutriate from this station contained concentrations of extractable organic compounds ranging from an estimated 43 to 420 micrograms per liter. Sediment elutriate samples were toxic to Ceriodaphnia dubta, Pimephales promelas, Photobacterium phosphoreum, and Salenastrum capricornulum.

Water-Resources Investigations Report↗
USGS1994

Quality of water and chemistry of bottom sediment in the Rillito Creek basin, Tucson, Arizona, 1986-92

Data were collected on physical properties and chemistry of 4 surface water, l4 ground water, and 4 bottom sediment sites in the Rillito Creek basin where artificial recharge of surface runoff is being considered. Concentrations of suspended sediment in streams generally increased with increases in streamflow and were higher during the summer. The surface water is a calcium and bicarbonate type, and the ground water is calcium sodium and bicarbonate type. Total trace ek=nents in surface water that exceeded the U.S. Environmental Protection Agency primary maximum contaminant levels for drinking-water standards were barium, beryllium, cadmium, chromium, lead, mercury and nickel. Most unfiltered samples for suspended gross alpha as uranium, and unadjusted gross alpha plus gross beta in surface water exceeded the U.S. Environmental Protection Agency and the State of Arizona drinking-water standards. Comparisons of trace- element concentrations in bottom sediment with those in soils of the western conterminous United States generally indicate similar concentrations for most of the trace elements, with the exceptions of scandium and tin. The maximum concentration of total nitrite plus nitrate as nitrogen in three ground- samples and total lead in one ground-water sample exceeded U.S. Environmental Protection Agency primary maximum contaminant levels for drinking- water standards, respectively. Seven organochlorine pesticides were detected in surface-water samples and nine in bottom-sediment samples. Three priority pollutants were detected in surface water, two were detected in ground water, and eleven were detected in bottom sediment. Low concentrations of oil and grease were detected in surface-water and bottom- sediment samples.

Water-Resources Investigations Report↗
USGS1996

Hydrologic and geochemical factors affecting the chemistry of small headwater streams in response to acidic deposition on Catoctin Mountain, north-central Maryland

Hydrologic and water-quality data were collected at a precipitation-collection station and from two small watersheds on Catoctin Mountain, north- central Maryland, as part of an investigation of episodic acidification and its effects on streamwater quality. Data were collected from June 1990 through December 1993. Descriptions of the water shed instrumentation, data-collection techniques, and laboratory methods used to conduct the studies are included. Data that were collected on precipitation, throughfall, soil water, ground water, and streamwater during base flow and stormflow indicate that the streams undergo episodic acidification during storms. Both streams showed decreases in pH to less than 5.0 standard units during stormflow. The acid-neutralizing capacity (ANC) of both streams decreased during stormflow, and the ANC of one of the streams, Bear Branch, became negative. The chemistries of the different types of waters that were sampled indicate that shallow subsurface water with minimal residence time in the watersheds is routed to the streams to become stormflow and is the cause of the episodic acidification observed. Three-component hydrograph separations were performed on the data collected during several storms in each watershed. The hydrograph separations of all of the storms indicate that throughfall contributed 0 to 50 percent of the stormflow, soil water contributed 0 to 80 percent, and ground water contributed 20 to 90 percent. The results of the hydrograph separations indicate that, in general, the watershed with higher hydraulic gradients tends to have shallower and shorter flow paths than the watershed with lower hydraulic gradients.

Maryland↗
USGS1996

Water-chemistry and chloride fluctuations in the Upper Floridan Aquifer in the Port Royal Sound area, South Carolina, 1917-93

Withdrawal of water from the Upper Floridan aquifer south of Port Royal Sound in Beaufort and Jasper Counties, South Carolina, has lowered water levels and reversed the hydraulic gradient beneath Hilton Head Island, South Carolina. Ground water that had previously discharged at the Sound is now being deflected southwest, toward withdrawals located near the city of Savannah, Georgia, and the island of Hilton Head. The reversal of this hydraulic gradient and the decline of water levels have caused saltwater in the Upper Floridan aquifer north of Port Royal Sound to begin moving southwest, toward water-supply wells for the town of Hilton Head and toward industries pumping ground water near Savannah. Analytical results from ground-water samples collected from wells in the Upper Floridan aquifer beneath and adjacent to Port Royal Sound show two plumes in the aquifer with chloride concentrations above the drinking- water standard. One plume of high chloride concentration extends slightly south of the theoretical predevelopment location of the steady- state freshwater-saltwater interface as indicated by numerical modeling. The other plume is present beneath the town of Port Royal, where the upper confining unit above the Upper Floridan aquifer is thin or absent. In these areas, the decline in water levels caused by ground-water withdrawals may have made it possible for water from tidal creeks to enter the Upper Floridan aquifer. Many wells completed in the upper permeable zone of the Upper Floridan aquifer show a distinct specific- conductance profile. One non-producing, monitoring well on Hilton Head Island (BFT-1810) was selected to depict a worst-case scenario to examine the short- and long-term water-chemistry and chloride fluctuations in the aquifer. Specific conductance was monitored at depths of 170, 190, and 200 feet below the top of the well casing. The specific conductance measured in 1987 ranged from approximately 450 microsiemens per centimeter near the top of the Upper Floridan aquifer to 1,500 microsiemens per centimeter near the lower, less permeable zone. Short-term fluctuations in conductance were measured at each probe and were found to be related to water-level fluctuations in the well caused by tidal cycles. The conductance varied regularly up to 100 microsiemens per centimeter, with an increasing time lag between high and low tides and low and high specific conductance for progressively shallower depths. Well BFT-1810 was monitored for specific conductance and water levels from October 1987 through September 1993. Specific conductance at the 170-foot probe showed little long-term change, while the 190- and the 200-foot probes showed long-term increases to approximately 4,000 and 10,000 microsiemens per centimeter, respectively. This well is located closest to one of the two plumes of saltwater delineated in the Upper Floridan aquifer, and the long-term chloride increases are a result of the movement of saltwater in the Upper Floridan aquifer toward Hilton Head Island under the influence of regional ground-water withdrawals.

South Carolina↗
USGS1997

Hydrogeology and water chemistry of Montezuma Well in Montezuma Castle National Monument and surrounding area, Arizona

Increasing population and associated residential and commercial development have greatly increased water use and consumption in the Verde Valley near Montezuma Well, a unit of Montezuma Castle National Monument in central Arizona. Flow from Montezuma Well and water levels in eight wells that are measured annually do not indicate that the ground-water system has been affected by development. Additional data are needed to develop an adequate ground-water monitoring program so that future effects of development can be detected. Monitoring the ground-water system would detect changes in discharge from the Montezuma Well or changes in the ground-water system that might indicate a potential change of flow to the well. Water samples were collected, and field measurements of specific conductance, pH, temperature, and dissolved oxygen were made throughout the pond at Montezuma Well during an exploration in May 1991. The exploration included two fissures in the bottom of the pond that were filled with sand. The sand in the fissures was kept in suspension by water entering the pond. Water chemistry indicates that the ground water from the area is a mixed combination of calcium, magnesium, sodium, and bicarbonate type water. The analyses for 18O/16O and 2H/1H show that the water from the wells and springs in the area, including Montezuma Well, has been exposed to similar environmental conditions and could have had similar flow paths. The MODFLOW finite-difference ground-water model was used to develop an uncalibrated interpretive model to study possible mechanisms for discharge of water at Montezuma Well. The study presents the hypothesis that ground water in the Supai Formation is the source of discharge to Montezuma Well because of the differences between the surface elevation of the pond at Montezuma Well and the stage in the adjacent Wet Beaver Creek. A series of simulations shows that upward flow from the Supai Formation is a possible mechanism for discharge to Montezuma Well, and that a geologic structure in the Supai Formation could play a role in the upward movement of water to Montezuma Well. The mechanism for inflow from the Verde Formation is not understood; however, this study concludes that the Verde Formation, Supai Formation, and other underlying rock units are probably the sources of water to Montezuma Well.

Water-Resources Investigations Report↗
USGS1998

Water quality in the vicinity of Mosquito Creek Lake, Trumbull County, Ohio, in relation to the chemistry of locally occurring oil, natural gas, and brine

Environmental samples collected in the Mosquito Creek Lake area were used to characterize water quality in relation to the chemistry of locally occurring oil, natural gas, and brine and to establish baseline water quality. Mosquito Creek Lake (a manmade reservoir) and the shallow bedrock aquifers near the lake are major sources of potable water in central Trumbull County. The city of Warren relies on the lake as a sole source of potable water. Some of the lake bottom may be in direct hydraulic connection with the underlying aquifers. The city of Cortland, along the southeastern shore of the lake, relies on the Cussewago Sandstone aquifer as a sole source of potable water. This aquifer subcrops beneath the glacio-fluvial sediments that underlie the lake. Nearly all residential homes around the lake, with the exception of homes in the city of Cortland, rely on domestic supply wells as a source of potable water. Oil and natural gas exploration and production have been ongoing in the Mosquito Creek Lakearea since the discovery of the historic Mecca Oil Pool in the Mississippian Berea and Cussewago Sandstones in 1860. Since the late 1970' s, the major drilling objective and zone of production is the Lower Silurian Clinton sandstone. The oil and natural gas resources of the Mosquito Creek Lake area, including reservoir pressure, production history, and engineering and abandonment practices are described in this report. The chemical and isotopic characteristics of the historic Mecca oil and natural gas are very different than those of the Clinton sandstone oil and natural gas. Gas chromatograms show that Mecca oil samples are extensively altered by biodegradation, whereas Clinton sandstone oils are not. Extensive alteration of Mecca oil is consistent with their occurrence at very shallow depths (less than 100 ft below land surface) where microbial activity can affect their composition. Also, the carbon-isotope composition of dissolved methane gas from Berea and Cussewago Sandstone water samples indicates that the gas is microbially generated, whereas the Clinton sandstone gases are thermogenically generated. Methane gas, in addition to crude oil, occurs naturally in the shallow Berea and Cussewago Sandstone aquifers in the Mosquito Creek Lake area and concentrations of dissolved methane are significant in the city of Cortland public-supply wells and in the domestic-supply wells near the southern shore of the lake. Water associated with oil and gas in the Clinton sandstone is a brine with high concentrations of chloride. Water from the Berea and Cussewago Sandstones, however, is fresh and potable. The contrasting geochemical characteristics are important for addressing water-quality issues that relate to oil and natural gas development in the Mosquito Creek area. A reexamination of the geologic framework and results of a subsurface-gas survey show that crude oil in the historic Mecca Oil Pool probably does not seep into Mosquito Creek Lake. Environmental samples show no evidence of any measurable release of oil, gas, or brine from the deeper Clinton sandstone oil and gas wells to the shallow aquifers, the lake, or lake tributaries. Brine is not associated with the hydrocarbons in the shallow Berea-Cussewago aquifer system and therefore cannot be a source of brine contamination. A mixing diagram constructed for dissolved bromide and chloride in surface water and water-supply wells shows no demonstrable mixing of these water resources with brine from the Clinton sandstone. There is some notable salinity in surface waters; however, the water is bromide poor, and a mixing diagram indicates that some local ground waters are influenced by halite solutions, presumably derived from leaching of road salt or from septic effluent.

Ohio↗
USGS2000

Ground-water and water-chemistry data for the Willamette basin, Oregon

This report presents ground-water data collected and compiled as part of a study of the ground-water resources of the Willamette River Basin, Oregon. The report includes tabulated information and a location map for 1,234 field-located water wells and 6 springs, hydrographs showing water-level fluctuations during various time periods for 265 of the wells, borehole geophysical data for 16 wells, and water-chemistry analyses from 125 wells and 6 springs. These data, as well as data for 4,752 additional fieldlocated wells and 1 spring, are included on a CD-ROM. In addition, the locations of the field-located wells and springs are provided in geographic information system formats on the CD-ROM.

Oregon↗
USGS1985

A primer on trace metal-sediment chemistry

In most aquatic systems, concentrations of trace metals in suspended sediment and the top few centimeters of bottom sediment are far greater than concentrations of trace metals dissolved in the water column. Consequently, the distribution, transport, and availability of these constituents can not be intelligently evaluated, nor can their environmental impact be determined or predicted solely through the sampling and analysis of dissolved phases. This Primer is designed to acquaint the reader with the basic principles that govern the concentration and distribution of trace metals associated with bottom and suspended sediments. The sampling and analysis of suspended and bottom sediments are very important for monitoring studies, not only because trace metal concentrations associated with them are orders of magnitude higher than in the dissolved phase, but also because of several other factors. Riverine transport of trace metals is dominated by sediment. In addition, bottom sediments serve as a source for suspended sediment and can provide a historical record of chemical conditions. This record will help establish area baseline metal levels against which existing conditions can be compared. Many physical and chemical factors affect a sediment's capacity to collect and concentrate trace metals. The physical factors include grain size, surface area, surface charge, cation exchange capacity, composition, and so forth. Increases in metal concentrations are strongly correlated with decreasing grain size and increasing surface area, surface charge, cation exchange capacity, and increasing concentrations of iron and manganese oxides, organic matter, and clay minerals. Chemical factors are equally important, especially for differentiating between samples having similar bulk chemistries and for inferring or predicting environmental availability. Chemical factors entail phase associations (with such sedimentary components as interstitial water, sulfides, carbonates, and organic matter) and ways in which the metals are entrained by the sediments (such as adsorption, complexation, and within mineral lattices).

Water Supply Paper↗
USGS2024

Editorial: From cold seeps to hydrothermal vents: Geology, chemistry, microbiology, and ecology in marine and coastal environments

This Research Topic compiles contemporary studies on cold seeps, hydrothermal vents, mud volcanoes, and related seafloor features that are associated with focused fluid emissions and the transfer of carbon, other chemical species, and sometimes heat from the geosphere to the ocean. Because these features sometimes tap fluids and gas originating kilometers below the seafloor, they provide an important window into deep processes that are otherwise inaccessible to scientists. At the shallow portion of their journey, migrating fluids nearing the seafloor contribute to a range of unique biological, physical, and chemical processes within the sediments themselves and at the sediment-water interface. Seafloor fluid emissions play a critical role in global biogeochemical cycles, ocean chemistry, and possibly even climate change. Seafloor leakage points often emit hydrocarbon gases (especially methane and CO 2 ) and are sometimes the loci for deposition of seafloor minerals that have economic value. A burgeoning area of research focuses on natural products generated at these features, seeking compounds with potential pharmaceutical or other applications. Multidisciplinary studies have become routine for characterization of seafloor fluid emission sites, attesting to the inseparability of geologic, physical, chemical, and biological processes in these settings. It is increasingly common for researchers to combine in a single research cruise: subbottom imaging and seafloor mapping; porewater and water column geochemistry and gas sampling; sediment retrieval for lithologic, biostratigraphic, and solid phase analyses; and studies of benthic and subseafloor communities at the microbial to macrofaunal scales. This multidisciplinary approach has the advantage of ensuring the spatial and temporal coincidence of surveys and samples, an important factor at highly dynamic seafloor fluid emission sites. In addition, researchers often use remotely operated vehicles (ROVs), autonomous underwater vehicles (AUVs), or human-occupied vehicles (HOVs) to record video of the seafloor, compile photomosaics, collect targeted samples, and survey with high-resolution geophysical near-seafloor systems, providing a degree of detail about seafloor fluid emission sites that is unprecedented compared to most areas of the deep ocean. While rarer, long-term cabled observatories or shorter-term deployments of portable observatories are also used at some loci for seafloor fluid flux and are particularly helpful for capturing temporal variations at these dynamic features. Here we summarize the Research Topic’s contribution to multidisciplinary seafloor emission studies in the categories of cold seeps, mud volcanoes, and hydrothermal vents. Figure 1 shows the geographic distribution of the studies in this Research Topic and key features referred to in this Introduction.

Frontiers in Earth Science↗
USGS2001

Hematological and serum chemistry norms for sandhill and whooping cranes

The normal values used as a diagnostic tool and for comparison of cranes were established in the early 1970's. In that early study, no effort was made to look at factors such as age, sex, or subspecies. In addition, during the early study disease problems (primarily disseminated visceral coccidiosis) and nutritional problems were undiagnosed and uncontrolled. For 2 years during the annual health examinations of cranes at the USGS Patuxent Wildlife Research Center (Patuxent), we collected blood from healthy cranes for analysis. We found significant differences between the values reported from the 1970's and the values seen in this study for 8 blood parameters for Florida sandhill cranes (Grus canadensis pratensis), 6 blood parameters for greater sandhill cranes (G. c. tabida), and 6 blood parameters for whooping cranes (Grus americana). In addition, there were significant differences for some hematology and serum chemistry values based on the age of the cranes.

Book chapter↗
USGS2002

Baseline hematology and clinical chemistry results from captive-raised trumpeter swans

Results from hematology and clinical chemistry tests are presented for healthy captive-raised Trumpeter Swans (Cygnus buccinator) to help establish baseline data. Blood samples were obtained from 14 cygnets between the ages of three to four and seven to eight months that were the subjects of a study to teach migration routes to swans. Males and females differed significantly in asparatate aminotransferase, alanine aminotransferase and total protein. Age categories differed significantly in hematocrit, white blood cell counts, alkaline phosphatase, aspar-rate aminotransferase, glucose, cholesterol and uric acid. There were no significant differences among age categories in values of alanine aminotransferase, calcium, triglycerides and total protein.

Book chapter↗
USGS2005

The effect of varying protein levels on blood chemistry, food consumption, and behavior of captive seaducks

The Chesapeake Bay is a primary wintering area for scoters and the long-tailed ducks (Clangia hyemalis) that migrate along the Atlantic Flyway. Recently, the Chesapeake Bay had undergone an ecosystem shift and little is known about how this is affecting the seaduck populations. We are determining what are the preferred food sources of the seaducks wintering on the Bay and analyzing the factors influencing prey selection whether it is prey composition, energy assimilated, prey availability, or a combination of any or all of these factors. We have established a captive colony of surf (Melanitta perspicillata) and white-winged scoters (Melanitta fusca) as well as long-tailed ducks at Patuxent Wildlife Research Center to allow us to examine these factors in a more controlled environment. This project contains a multitude of experiments and the resultant data will be compiled into a compartmental model on the feeding ecology of seaducks wintering on the Bay. The first experiment entailed feeding groups of each species (four ducks per pen of equal sex ratio, if possible, and four pens per species) three diets varying in percent protein levels from November to February. Each diet was randomly assigned to each pen and the amount of food consumed was recorded each day. New feed was given when all existing food was consumed. Behavioral trials and blood profiles were completed on all study birds to determine the effects of the varying diets. There were no significant differences in food consumption, blood chemistry, and behavior detected at the 5% level among the diets for all three species of interest. There was a seasonal effect determined based on the food consumption data for white-winged scoters, but not for surf scoters or long-tailed ducks. The blood profiles of the surf scoters were compared to blood profiles of wild surf scoters and a there was no difference detected at the 5% level. As a health check of the ducks an aspergillosis test was run on the blood obtained during the experiment and it was found that surf scoters are more resistant to the disease than the other species. In the next two winters natural prey items available to seaducks wintering in the Chesapeake Bay will be offered on palettes to examine preference without the additional energetic costs of diving. Assimilation efficiency trials will be run on all three species to determine amount of energy the ducks obtain from each food source. Finally, using two large aquariums, prey preference will be analyzed with the additional energetic costs of diving and searching for prey. In addition, we will determine the effect of availability of a prey item on the prey selection of seaducks. We hope the model created from these experiments will allow managers to examine the effects of changes in the benthos on the seaduck populations wintering in the Chesapeake Bay.

Book chapter↗
USGS2006

Macroinvertebrate abundance, water chemistry, and wetland characteristics affect use of wetlands by avian species in Maine

Our objective was to determine use by avian species (e.g., piscivores, marsh birds, waterfowl, selected passerines) of 29 wetlands in areas with low (<200 ueq 1-1) acid-neutralizing capacity (ANC) in southeastern Maine. We documented bird, pair, and brood use during 1982?1984 and in 1982 we sampled 10 wetlands with a sweep net to collect invertebrates. We related mean numbers of invertebrates per wetland to water chemistry, basin characteristics, and avian use of different wetland types. Shallow, beaver (Castor canadensis)-created wetlands with the highest phosphorus levels and abundant and varied macrophyte assemblages supported greater densities of macroinvertebrates and numbers of duck broods (88.3% of all broods) in contrast to deep, glacial type wetlands with sparse vegetation and lower invertebrate densities that supported fewer broods (11.7%). Low pH may have affected some acid-intolerant invertebrate taxa (i.e., Ephemeroptera), but high mean numbers of Insecta per wetland were recorded from wetlands with a pH of 5.51. Other Classes and Orders of invertebrates were more abundant on wetlands with pH > 5.51. All years combined use of wetlands by broods was greater on wetlands with pH < 5.51 (77.4%) in contrast to wetlands with pH > 5.51 that supported 21.8% of the broods. High mean brood density was associated with mean number of Insecta per wetland. For lentic wetlands created by beaver, those habitats contained vegetative structure and nutrients necessary to provide cover to support invertebrate populations that are prey of omnivore and insectivore species. The fishless status of a few wetlands may have affected use by some waterfowl species and obligate piscivores.

Conference Paper↗
USGS1985

Growth and blood chemistry of ducklings reared on acidified wetlands

Acid deposition is one factor that may be responsible for the decline of some waterfowl populations. Growth and physiological condition were monitored in captive-reared black ducks (Anas rubripes) exposed for 10-day trials (day 11-20 of life) on control (pH 6.8) and acidified (pH 5.0) man-made emergent wetlands. Impaired growth (body weight, culmen and tarsus length) and increased mortality (50%) were apparent in broods (hen + 4 ducklings) reared on acidified wetIands. Ducklings exbibiting poor growth had reduced hematocrit, plasma protein and cholesterol levels. This subset of birds had elevated plasma uric acid concentration and creatine kinase activity (perhaps due to enhanced protein and nucleotide catabolism). and elevated pIasma K+ levels. Based upon overt appearance, growth and blood chemistry, ducklings exposed to acidified wetlands were concluded to be in poorer condittion than those exposed on circumneutral pH wetlands.

American Zoologist↗
USGS1989

The evolution of thermal structure and water chemistry in Lake Nyos

We collected a time series of physical and chemical data to gain a better understanding of the dynamics of Lake Nyos. Measurements of water and gas chemistry, and temperature made during January, March, and May 1987 are compared to data taken in September 1986 just after the initial CO2 gas release. There is no pattern of change in overall heat content of the lake, although heat input to bottom waters (185-208 m) has occurred at a rate of 1600 mW m-2. This increase in heat content translates to a change from 23.38 to 24.12??C at 200 m and can be explained by geothermal heat flow and addition of thermal spring water. Concentrations of Ca2+, Mg2+, Na+, K+, Fe2+ and alkalinity have increased only in bottom waters. In situ lake processes such as sulfate and iron reduction are unable to account for the changes in alkalinity. Observed chemical changes are consistent with a scenario where slightly thermal soda water is being input to the bottom of the lake. Measurements of pCO2 at depth ranged from 18 to 28% of saturation and exhibited horizontal variability. Overall recharge of CO2 in bottom waters is negligible. Mainly because of increasing ion concentrations in bottom water, total stability of the water column increased 33% from 48,800 J m-2 in September 1986 to 64,700 J m-2 in May 1987. As long as CO2 concentrations remain the same, this level of stability is higher than could be disrupted by common limnologic or meteorologic processes. There is thermal and chemical evidence that a buildup of dissolved iron and CO2 in bottom waters must have preceded the August 1986 gas release. In addition, a survey of all crater lakes in Cameroon indicates that only Lakes Nyos and Monoun contain high concentrations of dissolved iron and CO2. Thus there is a low probability of any other Cameroonian lake releasing a substantial volume of CO2. ?? 1989.

Journal of Volcanology and Geothermal Research↗
USGS1990

Crystal chemistry of the natural vanadium bronzes

The crystal chemistry of the natural vanadium bronze minerals is reviewed on the basis of published information and new studies (mainly by X-ray powder-diffraction methods) using type material wherever possible. The known V bronze minerals are divided into three categories: 1) the hewettite group, 2) the straczekite group, 3) other structure types including navajoite, schubnelite, fervanite, shcherbinaite, bannermanite, and melanovanadite. All known structures associated with the fibrous V bronzes (fiber spacing 3.6 A??) can be considered as various lateral linkages (into sheets or networks) of only two types of polyvanadate chains: 1) a divanadate chain (V2O6)n consisting of alternating square pyramids, and 2) a tetravanadate chain (V4O12)n consisting of four highly condensed single octahedral chains. -from Authors

American Mineralogist↗
USGS1994

The crystal structure and crystal chemistry of fernandinite and corvusite

Using type material of fernandinite from Minasragra, Peru, and corvusite from the Jack Claim, La Sal Mountains, Utah, the properties and crystal chemistry of these minerals have been determined by Rietveld analysis of the powder X-ray-diffraction patterns. The crystal structure of both species is isotypic with the V2O5 -type layer first found for ??-Ag0.68V2O5; it consists of chains of VO6 octahedra linked by opposite corners (parallel to b) condensed by edge-sharing to form the layer. The vanadium has average valence 4.8, and the resulting layer-charge is balanced by varying amounts of Ca, Na, and K in the interlayer region accompanied by labile water. This study has confirmed the validity of fernandinite as a unique mineral species. It is closely related to corvusite, from which it is distinguished on the basis of the dominant interlayer cation: Ca for fernandinite, Na for curvusite. -Authors

Canadian Mineralogist↗