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At least 577 records · Page 32Linked to original sources
USGS1886

Report of work done in the division of chemistry and physics mainly during the fiscal year 1884-85

The present bulletin contains some of the more important results obtained in the chemical laboratory of the United States Geological Survey during the fiscal year 1884—'85. It also contains two physical papers representing work which was mainly done during previous fiscal years, but completed during the one for which this bulletin is issued. These papers are practically continuations of or supplements to Bulletin 14.

Bulletin↗
USGS1990

Chemistry and mineralogy of natural bitumens and heavy oils and their reservoir rocks from the United States, Canada, Trinidad and Tobago, and Venezuela

Twenty-one samples from natural bitumen and heavy oil deposits in seven States of the United States and six samples from outside the United States form the basis of this initial study. This Circular gives the mineral content of the reservoir rock, the trace-element distribution in the reservoir rock and hydrocarbons, and the composition of the heavy oil and natural bitumen. The reservoir rock and sediment residues from California contain more trace-element maximum amounts than any of the other rock samples. These relatively high concentrations of trace elements may be due, in part, to the low quartz content of the rock and to the presence of heulandite, cristobalite, siderite, and pyrite. The reservoir rock and sediment residues from Oklahoma contain more minimum amounts of trace elements than any of the other rock samples. This pattern probably results from the large amount of quartz in four of the samples and a large amount of calcite in the other sample. The maximum and minimum amounts of trace elements in the bitumen and heavy oil do not correlate with those in the reservoir rocks. The bitumen from Utah contains the greatest number of trace-element maxima, whereas there is no trend in the trace-element minima in the bitumen and heavy oil.

Circular↗
USGS2007

Soil and sediment chemistry in the Mississippi River Delta following Hurricane Katrina

In October 2005, the U.S. Geological Survey's (USGS) Mid-Continent Geographic Science Center and the University of Missouri-Rolla's (UMR) Environmental Research Center for Emerging Contaminants partnered to collect perishable environmental data along the Mississippi River Delta to catalog the effects of Hurricane Katrina, a category 3 storm that caused nearly complete destruction to the delta's population support structure and industry. The data presented here begin the process of characterizing the chemical composition of sediments and soil along the delta following this significant natural disaster.

Louisiana↗
USGS2007

Effects of Hurricanes Katrina and Rita on the chemistry of bottom sediments in Lake Pontchartrain, La.

Concerns about the effect of pumping contaminated flood waters into Lake Pontchartrain following the hurricanes of 2005 prompted the U.S. Geological Survey (USGS) to sample street mud, canal-suspended sediment, and bottom sediment in Lake Pontchartain. The samples were analyzed for a wide variety of potential inorganic and organic contaminants. Results indicate that contamination of lake sediment relative to other urban lakes and to accepted sedimentquality guidelines was limited to a relatively small area offshore from the Metairie Outfall Canal (popularly known as the 17th Street Canal) and that this contamination is probably transient.

Louisiana↗
USGS1983

Evidence for acid-precipitation-induced trends in stream chemistry at hydrologic bench-mark stations

Ten- to 15-year water-quality records from a network of headwater sampling stations show small declines in stream sulfate concentrations at stations in the northeastern quarter of the Nation and small increases in sulfate at most southeastern and western sites. The regional pattern of stream sulfate trends is similar to that reported for trends in S02 emissions to the atmosphere during the same period. Trends in the ratio of alkalinity to total major cation concentrations at the stations follow an inverse pattern of small increases in the Northeast and small, but widespread decreases elsewhere. The undeveloped nature of the sampled basins and the magnitude and direction of observed changes in relation to SO2 emissions support the hypothesis that the observed patterns in water quality trends reflect regional changes in the rates of acid deposition.

Circular↗
USGS2007

Aquatic Communities and Selected Water Chemistry in St. Vrain Creek near the City of Longmont, Colorado, Wastewater-Treatment Plant, 2005 and 2006

In 2005, the U.S. Geological Survey and the City of Longmont, Colo., began a study to document chemical characteristics of St. Vrain Creek that had previously been unavailable either due to high cost of analysis or lack of analytical capability. Stream samples were collected at seven sites on St. Vrain Creek during the spring of 2005 and 2006 for analysis of wastewater compounds. A Lagrangian-sampling design was followed during each sampling event, and time-of-travel studies were conducted just prior to each sampling event to determine appropriate sampling times for the synoptic. In addition, semipermeable membrane devices, passive samplers that concentrate hydrophobic organic chemicals, were installed at six sites during the spring of 2005 and 2006 for approximately 4 weeks. After retrieval, contaminant residues concentrated in the semipermeable membrane devices were recovered and used in a toxicity assay that provided a screen for aryl hydrocarbon receptor type compounds, including polycyclic aromatic hydrocarbons, polychlorinated biphenyls, dioxins, and furans. In addition, the U.S. Geological Survey summarized information on macroinvertebrate and fish communities known from St. Vrain Creek dating back to the early 1900s in order to assess their utility in evaluating wastewater-treatment plant upgrades and habitat improvement projects. Unfortunately, because of inconsistencies in data collection these data cannot be used as intended; however, they are useful for understanding to some degree gross patterns in fish species distribution, but less so for macroinvertebrates.

Data Series↗
USGS2012

Water chemistry and electrical conductivity database for rivers in Yellowstone National Park, Wyoming

Chloride flux has been used to estimate heat flow in volcanic environments since the method was developed in New Zealand by Ellis and Wilson (1955). The method can be applied effectively at Yellowstone, because nearly all of the water discharged from its thermal features enters one of four major rivers (the Madison, Yellowstone, Snake, and Falls Rivers) that drain the park, and thus integration of chloride fluxes from all these rivers provides a means to monitor the total heat flow from the entire Yellowstone volcanic system (Fournier and others, 1976; Fournier, 1979). Fournier (1989) summarized the results and longterm heat-flow trends from Yellowstone, and later efforts that applied the chloride inventory method to estimate heat flow were described by Ingebritsen and others (2001) and Friedman and Norton (2007). Most recently, the U.S. Geological Survey (USGS), in conjunction with the National Park Service, has provided publicly accessible reports on solute flux, based on periodic sampling at selected locations (Hurwitz and others, 2007a,b). While these studies have provided a wealth of valuable data, winter travel restrictions and the great distances between sites present significant logistical challenges and have limited collection to a maximum of 28 samples per site annually. This study aims to quantify relations between solute concentrations (especially chloride) and electrical conductivity for several rivers in Yellowstone National Park (YNP), by using automated samplers and conductivity meters. Norton and Friedman (1985) found that chloride concentrations and electrical conductivity have a good correlation in the Falls, Snake, Madison, and Yellowstone Rivers. However, their results are based on limited sampling and hydrologic conditions and their relation with other solutes was not determined. Once the correlations are established, conductivity measurements can then be used as a proxy for chloride concentrations, thereby enabling continuous heat-flow estimation on a much finer timescale and at lower cost than is currently possible with direct sampling. This publication serves as a repository for all data collected during the course of the study from May 2010 through July 2011, but it does not include correlations between solutes and conductivity or recommendations for quantification of chloride through continuous electrical conductivity measurements. This will be the object of a future document.

Wyoming↗
USGS2025

Exploring atmospheric deposition chemistry data across the United States

The National Atmospheric Deposition Program (NADP) collects atmospheric data to monitor air pollution effects on the quality of United States water supplies and ecosystems. The NADP requires consistent data collection at fixed locations and is governed by a committee with participation by many Federal and State agencies, universities, Tribes, and private companies. NADP conducts a spring business meeting where the Network Operations, Education and Outreach, and multiple science subcommittees adjourn to discuss all aspects of NADP. Similar to the spring meeting, a fall meeting occurs with the addition of a two-day scientific symposium where scientists present their research using NADP data.

Fact Sheet↗