Analysis of Arsenic Uptake by Plant Species Selected for Growth in Northwest Ohio by Inductively Coupled Plasma–Optical Emission Spectroscopy

Abstract

Arsenic (As) contamination is widespread in the industrial areas of northwest Ohio. Plant species that both take up As and are appropriate for the climate and growth conditions of the region are needed for phytoremediation to be successfully employed. Actively growing plants from 22 species of native genera were exposed to As in hydroponics systems (either 0, 10, or 50 mg As L^?1; 1 week) and commercially available potting mix (either 0, 10, 25, 100, or 250 mg As L^?1; 2 weeks), depending on their growth conditions. Aboveground plant tissues were harvested and digested, and concentrations of As were determined by inductively coupled plasma–optical emission spectrometry. The highest tissue concentrations of As (mg As kg^?1 dw) were recorded in seven plant species: Rudbeckia hirta (661), Helenium autumnale (363 in tissues formed after exposure to As), Lupinus perennis (333), Echinacea purpurea (298), Coreopsis lanceolata (258), Lepidium virginicum (214), and Linum lewisii (214). These seven species are ecologically diverse, which suggests that phytoremediation of As using diverse assemblages of plants may be an option for a variety of environments.     

Comparative Evaluation of Inductively Coupled Plasma–Optical Emission Spectroscopy and Atomic Absorption Spectrophotometry for Determining DTPA-Extractable Micronutrients in Soils

A study was conducted for comparative evaluation of atomic absorption spectrophotometry (AAS) and inductively coupled plasma–optical emission spectroscopy (ICP-OES) for determining extractable zinc (Zn), copper (Cu), manganese (Mn), and iron (Fe) in sixty diverse soil samples having a wide range in pH and organic carbon (C). The results were significantly affected by the method of analysis and soil type but generally did not follow a definite trend. Results for extractable Fe in Alfisol samples were significantly greater when using ICP-OES than AAS; and the results for Zn, Cu, and Mn were not significantly different for the two methods. For Vertisol samples, the results for extractable Cu were significantly greater by ICP-OES than by AAS, whereas extractable Fe and Zn were significantly greater by AAS than by ICP-OES, and the results for Mn were not significantly different for the two methods. The results are discussed relative to soil type and differences in soil organic carbon and pH of the samples used in the study.     

Determination of Major and Trace Elements in Plant Samples by Inductively Coupled Plasma–Mass Spectrometry

The determination of several trace elements [arsenic (As), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), molybdenum (Mo), nickel (Ni), and lead (Pb)] in plant samples using inductively coupled plasma–mass spectrometry (ICP‐MS) was evaluated. It was established experimentally that moderate amounts (0.2–2%) of dissolved solids decreased the analyte signals significantly. Internal standardization with Rh was efficiently used to compensate for these matrix effects. The accuracy of the method was verified using reference materials digested according to two different procedures: dry ashing and microwave digestion. No significant differences were observed between measured concentrations and certified values. The investigation was next extended for the determination of major elements [aluminum (Al), boron (B), calcium (Ca), iron (Fe), potassium (K), magnesium (Mg), manganese (Mn), sodium (Na), phosphorus (P), and zinc (Zn)] on the same reference materials. The ICP‐MS values agree well with the values supplied. However, it appeared that Sc was the most useful internal standard for major elements.     

Spectrophotometric and Inductively Coupled Plasma–Optical Emission Spectroscopy Determination of Gallium in Natural Soils and Soils Polluted by Industry: Relationships between Elements

The aim of this work was to determine gallium contents in different soils of Poland using a sensitive spectrophotometric method based on the complex of Ga(III) with chrome azurol S and benzyldodecyldimethylammonium bromide and inductively coupled plasma–optical emission spectrometry technique. The total content of gallium in the soils clearly depends on the soil location and properties and ranged from 41.7 to 437 μg g^–1. The contents of gallium determined in 10% nitric acid and 1 M of magnesium chloride extract ranges respectively from 38.0 to 81.9% and 20–40% of the total content of this element. A strong correlation has been found between gallium and zinc, cadmium, lead, and copper. The high Pearson correlation coefficient values and the proportional relationship between the concentrations of Ga and these metals may make it possible to treat gallium as an indicator of soil contamination with heavy metals.     

Comparative Evaluation of Inductively Coupled Plasma–Atomic Emission Spectroscopy and Colorimetric Methods for Determining Hot-Water-Extractable Boron in Soils

Frequency of boron (B) deficiency is increasing in rainfed systems, and hence there is a need to diagnose the deficiency. Colorimetric methods are still widely used in soil-testing laboratories in India for measuring B. Little information is available on the comparative evaluation of the colorimetric and inductively coupled plasma (ICP) methods for determining extractable B in soils. We describe results of the comparative evaluation of these methods for measuring extractable B in 57 soil samples with pH values ranging from 5.3 to 9.5. There was a significant correlation between B values determined by the two methods, and the correlation coefficient was greater for soil samples with pH in the neutral to alkaline range. Interaction between soil samples and methods (ICP or colorimetric) was significant except for soil samples in the pH range of 8.0 to 9.5. Precision for B determination was greater with the ICP than with the colorimetric method.