Howard E. Taylor

An Inductive-coupled Plasma Atomic-Emission Spectrometric Method for Routine Water Quality Testing

Induction-coupled plasma atomic-emission spectrometry offers an ideal method for simultaneous multielement analysis of natural water samples. The Water Resources Division of the U.S. Geological Survey currently employs this technique for quantitative analysis of 17 major and trace constituents. These include analysis of Ba, Be, Cd, Co, Cu, Fe, Pb, Li, Mn, Sr, Mo, V, Zn, Ca, Mg, Na, and SiO2 in a routine production mode, in which an excess of 1000 determinations can be made in a normal working day. Comparability studies with conventional single-element methods of analysis, such as atomic absorption spectrometry and colorimetric techniques, show essentially equivalent accuracy and precision, frequently at much higher sensitivity.

Mercury on the move during snowmelt in Vermont

Although mercury (Hg) emissions peaked in the United States over the last 20 to 40 years and are now declining, they remain well above natural background levels in soils and sediments. Only a small fraction of the Hg deposited from the atmosphere to the terrestrial landscape runs off in streamflow. However, some of this Hg is methylated in the environment and can potentially bioaccumulate to the top of food webs, posing a hazard to people who eat fish, especially children and pregnant women. What factors determine the amount of Hg that runs off in streams? During the 2000 snowmelt at Sleepers River in Vermont, strong correlations were found between dissolved and particulate mercury and the respective dissolved and particulate organic carbon fractions, even when data were pooled from 10 streams of diverse watershed size and land cover. Episodic export of particulate Hg during the highest flows appears to be the dominant mechanism of Hg movement.

Ancient maize from Chacoan great houses: Where was it grown?

In this article, we compare chemical (87Sr/86Sr and elemental) analyses of archaeological maize from dated contexts within Pueblo Bonito, Chaco Canyon, New Mexico, to potential agricultural sites on the periphery of the San Juan Basin. The oldest maize analyzed from Pueblo Bonito probably was grown in an area located 80 km to the west at the base of the Chuska Mountains. The youngest maize came from the San Juan or Animas river floodplains 90 km to the north. This article demonstrates that maize, a dietary staple of southwestern Native Americans, was transported over considerable distances in pre-Columbian times, a finding fundamental to understanding the organization of pre-Columbian southwestern societies. In addition, this article provides support for the hypothesis that major construction events in Chaco Canyon were made possible because maize was brought in to support extra-local labor forces.

Anthropogenic tracers, endocrine disrupting chemicals, and endocrine disruption in Minnesota lakes

Concentrations of endocrine disrupting chemicals and endocrine disruption in fish were determined in 11 lakes across Minnesota that represent a range of trophic conditions and land uses (urban, agricultural, residential, and forested) and in which wastewater treatment plant discharges were absent. Water, sediment, and passive polar organic integrative samplers (POCIS) were analyzed for steroidal hormones, alkylphenols, bisphenol A, and other organic and inorganic molecular tracers to evaluate potential non-point source inputs into the lakes. Resident fish from the lakes were collected, and caged male fathead minnows were deployed to evaluate endocrine disruption, as indicated by the biological endpoints of plasma vitellogenin and gonadal histology. Endocrine disrupting chemicals, including bisphenol A, 17β-estradiol, estrone, and 4-nonylphenol were detected in 90% of the lakes at part per trillion concentrations. Endocrine disruption was observed in caged fathead minnows and resident fish in 90% of the lakes. The widespread but variable occurrence of anthropogenic chemicals in the lakes and endocrine disruption in fish indicates that potential sources are diverse, not limited to wastewater treatment plant discharges, and not entirely predictable based on trophic status and land use.

Inductively coupled plasma-mass spectrometry as an element-specific detector for field-flow fractionation particle separation

An inductively coupled plasma-mass spectrometer was used for the quantitative measurement of trace elements In specific,submicrometer size-fraction particulates, separated by sedimentation field-flow fractionation. Fractions were collected from the eluent of the field-flow fractionation centrifuge and nebulized, with a Babington-type pneumatic nebulizer, into an argon inductively coupled plasma-mass spectrometer. Measured Ion currents were used to quantify the major, minor, and trace element composition of the size-separated colloidal (< 1-microm diameter) particulates. The composition of surface-water suspended matter collected from the Yarra and Darling rivers in Australia is presented to illustrate the usefulness of this tool for characterizing environmental materials. An adsorption experiment was performed using cadmium lon to demonstrate the utility for studying the processes of trace metal-suspended sediment interactions and contaminant transport in natural aquatic systems.

A direct differential pulse anodic stripping voltammetric method for the determination of thallium in natural waters

Abstract A dual direct method for the ultratrace determination of thallium in natural waters by differential pulse anodic stripping voltamrnetry (d.p.a.s.v.) is presented. D.p.a.s.v. at the hanging mercury drop electrode and at the mercury film electrode is used in the concentration ranges 0.5–100 μg Tl l-1, and 0.01–10 μg Tl l-1, respectively. Quantification is aided by the technique of standard additions. The response of the method is optimized for typical natural surface water matrices. An intercomparison of thalium determinations performed by the two anodic stripping methods and electrothermal-atomization atomic absorption spectrometry on normal and thallium-spiked surface water samples demonstrates equivalent accuracy within the range where atomic absorption is applicable. The method appears free from serious interferences.

Mississippi river methods comparison study: Implications for water quality monitoring of dissolved trace elements

Recent reports have questioned the validity of dissolved trace element concentrations reported by the U.S. Geological Surveys National Stream Quality Accounting Network (NASQAN) as well as by other water-quality monitoring programs. To address these concerns and to evaluate the NASQAN protocols, the U.S. Geological Survey undertook the Mississippi River Methods Comparison Study. We report here the major results and implications of this study. In particular, we confirm the possible inaccuracy of previous NASQAN dissolved trace element data. The results suggest that all steps of the NASQAN protocol (sampling, processing, and analysis) require revision, though the sample filtration step appears to be of particular concern

Snow chemistry of the Cascade-Sierra Nevada Mountains.

This investigation assesses geographic variations in atmospheric deposition in Washington, Oregon, and California using snow cores from the Cascade-Sierra Nevada Mountains, collected from late February to mid-March 1983. A statistical analysis of the analytical and sampling precision was made. The snowpack in the higher Cascades and Sierra Nevada is not strongly influenced by anthropogenic activities at present. The pH of snow samples ranges from 5.11 to 5.88. Sulfate and nitrate correlate with H/sup +/ in some segments of the sample traverse. The SO/sub 4/ data show apparent influence from major source areas in Washington and California; nitrate does not. An apparent decrease in NH/sub 4/ in snow in Washington and California suggests atmospheric interactions resulting in the removal of NH/sub 4/. The NH/sub 4/ reduction raises questions about nutrient supply in the mountain vegetation. Heavy-metal correlations included Cd, Cu, and Fe with Pb, and Mn with K and DOC, among others. No correlation was found between constituents and snow-water content. 47 references, 11 figures, 7 tables.

A Babington-type Nebulizer for Use in the Analysis of Natural Water Samples by Inductively Coupled Plasma Spectrometry

The construction and evaluation of a Babington-type pneumatic nebulizer for use in the inductively coupled plasma, emission spectrometric analysis of natural water samples is described. The performance of the nebulizer is relatively insensitive to suspended particulate matter, and detection limits for a wide variety of elements are equivalent to or better than those achieved with other pneumatic nebulizers. An accuracy comparison with a conventional crossflow pneumatic nebulizer shows essentially no analysis bias.

The Western Airborne Contaminant Assessment Project (WACAP): An Interdisciplinary Evaluation of the Impacts of Airborne Contaminants in Western U.S. National Parks

The National Park Service Organic Act of 1916 (1) required protection of the national parks for perpetuity by tasking the National Park Service (NPS) to maintain these lands “...unimpaired for the enjoyment of future generations.” Near the close of the last century, the NPS became aware of a new body of research describing a potential ecosystem threat that could not be ignored. Toxic airborne contaminants were increasingly being found in the world’s most pristine alpine and polar ecosystems, far from where such chemicals were produced or used, and the risks to the national parks of the western U.S. were unknown. Airborne contaminants present a broad range of potential risks to these ecosystems, largely due to bioaccumulation and or biomagnification of toxicants in biota, particularly vertebrates, that can result in loss of fecundity, unfit offspring, maladaptive behavior, and even death. As an outgrowth of these concerns, the Western Airborne Contaminants Assessment Project (WACAP) was initiated in 2002 to determine the risk from airborne contaminants to ecosystems and food webs in national parks of the U.S. The specific objectives that guided design and implementation of WACAP were the following: 1. Determine if contaminants were present in western national parks. 2. If contaminants were present, determine in what way and where they were accumulating (geographically and by elevation). EP A Environ. Sci. Technol. 2010, 44, 855–859