Raina Margaret Maier

Raina Margaret Maier

Professor, Environmental Science
Professor, Pharmaceutical Sciences
Professor, Pharmacology and Toxicology
Professor, BIO5 Institute
Primary Department
Department Affiliations
Contact
(520) 621-7231

Research Interest

Raina M Maier, PhD, is a Professor of Environmental Microbiology in the Department of Soil, Water and Environmental Science and Director of the University of Arizona NIEHS Superfund Research Program. She also serves as Director of the University of Arizona Center for Environmentally Sustainable Mining and as Deputy Director of the TRIF Water Sustainability Program. Dr. Maier is internationally known for her work on microbial surfactants (biosurfactants) including discovery of a new class of biosurfactants and of novel applications for these unique materials in remediation and green technologies. She is also recognized for her work on the relationships between microbial diversity and ecosystem function in oligotrophic environments such as carbonate caves, the Atacama desert, and mine tailings. Dr. Maier has published over 100 original research papers, authored 23 book chapters, and holds a patent on the use of biosurfactants to control zoosporic plant pathogens. She is the lead author on the textbook “Environmental Microbiology” currently in its second edition.Dr. Maier emphasizes a multidisciplinary approach to her work and has served as PI or co-PI on several large granting efforts including the UA NIEHS Superfund Research Program, the UA NSF Kartchner Caverns Microbial Observatory, and the UA NSF Collaborative Research in Chemistry grant on biosurfactants.

Publications

Hayes, S. M., Webb, S. M., Bargar, J. R., O'Day, P. A., Maier, R. M., & Chorover, J. (2012). Geochemical weathering increases lead bioaccessibility in semi-arid mine tailings. Environmental science & technology, 46(11), 5834-41.

Mine tailings can host elevated concentrations of toxic metal(loid)s that represent a significant hazard to surrounding communities and ecosystems. Eolian transport, capable of translocating small (micrometer-sized) particles, can be the dominant mechanism of toxic metal dispersion in arid or semiarid landscapes. Human exposure to metals can then occur via direct inhalation or ingestion of particulates. The fact that measured doses of total lead (Pb) in geomedia correlate poorly with blood Pb levels highlights a need to better resolve the precise distribution of molecularly speciated metal-bearing phases in the complex particle mixtures. Species distribution controls bioaccessibility, thereby directly impacting health risk. This study seeks to correlate Pb-containing particle size and mineral composition with lability and bioaccessibility in mine tailings subjected to weathering in a semiarid environment. We employed X-ray absorption spectroscopy (XAS) and X-ray fluorescence (XRF), coupled with sequential chemical extractions, to study Pb speciation in tailings from the semiarid Arizona Klondyke State Superfund Site. Representative samples ranging in pH from 2.6 to 5.4 were selected for in-depth study of Pb solid-phase speciation. The principle lead-bearing phase was plumbojarosite (PbFe(6)(SO(4))(4)(OH)(12)), but anglesite (PbSO(4)) and iron oxide-sorbed Pb were also observed. Anglesite, the most bioavailable mineral species of lead identified in this study, was enriched in surficial tailings samples, where Pb concentrations in the clay size fraction were 2-3 times higher by mass relative to bulk. A mobile and bioaccessible Pb phase accumulates in surficial tailings, with a corresponding increase in risk of human exposure to atmospheric particles.

Sandrin, T. R., & Maier, R. M. (2002). Effect of pH on cadmium toxicity, speciation, and accumulation during naphthalene biodegradation. Environmental Toxicology and Chemistry, 21(10), 2075-2079.

PMID: 12371483;Abstract:

Lowering pH of a microbiological medium from 7 to 4 decreased cadmium toxicity during naphthalene biodegradation by a Burkholderia sp. Cadmium speciation and cadmium accumulation in the system were studied to explain this effect. Cadmium speciation was determined by direct measurement and by geochemical modeling. Previous studies have implicated the monovalent hydroxylated cadmium (CdOH+) species in the effect of pH on cadmium toxicity. Modeling analysis predicted CdOH+ formation only at very low concentrations (≤0.0128 μM), while the measured concentration of divalent ionic cadmium (Cd2+) was at least three orders of magnitude greater, suggesting that Cd2+ is the more significant metal form. With respect to cadmium accumulation, cells contained in media adjusted to pH 4 accumulated only 2.76 ± 0.76 mg Cd/g cells, whereas cells in media adjusted to pH 7 accumulated 8.52 ± 0.71 mg Cd/g cells. These data suggest that cadmium toxicity is correlated with increased cadmium accumulation rather than the formation of CdOH+ as pH is increased. At low pH, the decrease in cadmium accumulation may be caused by increased competition between hydrogen and cadmium ions for binding sites on the cell surface or by an increase in metal efflux pump activity due to an increase in the proton gradient that drives the efflux pump.

de-Bashan, L. E., Hernandez, J. P., Nelson, K. N., Bashan, Y., & Maier, R. M. (2010). Growth of quailbush in acidic, metalliferous desert mine tailings: effect of Azospirillum brasilense Sp6 on biomass production and rhizosphere community structure. Microbial ecology, 60(4), 915-27.

Mine tailing deposits in semiarid and arid environments frequently remain devoid of vegetation due to the toxicity of the substrate and the absence of a diverse soil microbial community capable of supporting seed germination and plant growth. The contribution of the plant growth promoting bacterium (PGPB) Azospirillum brasilense Sp6 to the growth of quailbush in compost-amended, moderately acidic, high-metal content mine tailings using an irrigation-based reclamation strategy was examined along with its influence on the rhizosphere bacterial community. Sp6 inoculation resulted in a significant (2.2-fold) increase in plant biomass production. The data suggest that the inoculum successfully colonized the root surface and persisted throughout the 60-day experiment in both the rhizosphere, as demonstrated by excision and sequencing of the appropriate denaturing gradient gel electrophoresis (DGGE) band, and the rhizoplane, as indicated by fluorescent in situ hybridization of root surfaces. Changes in rhizosphere community structure in response to Sp6 inoculation were evaluated after 15, 30, and 60 days using DGGE analysis of 16S rRNA polymerase chain reaction amplicons. A comparison of DGGE profiles using canonical correspondence analysis revealed a significant treatment effect (Sp6-inoculated vs. uninoculated plants vs. unplanted) on bacterial community structure at 15, 30, and 60 days (p  0.05). These data indicate that in an extremely stressed environment such as acid mine tailings, an inoculated plant growth promoting bacterium not only can persist and stimulate plant growth but also can directly or indirectly influence rhizobacterial community development.

Miller, R. M., Stitzer, L. S., Artiola, J. F., & Fuller, W. H. (1992). Effect of four alcohols on adsorption, desorption, and movement of cadmium, nickel, and zinc through soils. Chemosphere, 24(12), 1855-1866.

Abstract:

Miscible-displacement experiments were conducted to compare the effects of aqueous soil solutions with ethyl alcohol, ethylene glycol, diethylene glycol, and triethylene glycol on the movement of metals through soils. Aqueous or alcohol solutions containing 1 mM each Cd, Ni, and Zn and 5 mM Ca were perfused through columns containing River Sand, Canelo loam (Canelo I) or Mohave sandy clay loam (Mohave scl) until effluent metal concentrations (C) equaled influent concentrations (CO) or CC0-1 = 1. In general, the order of sorption was Zn > Ni > Cd in aqueous-perfused columns, while in alcohol-perfused columns sorption of M > > Cd ≥ Zn. In comparison to aqueous solutions, alcohols reduced total metal sorption by at least 25%. Metal sorption was best correlated to cation exchange capacity of the soil, sorption of metals being greatest in the Mohave scl and least in the River Sand. After CC0-1 = 1 was reached, columns were leached with deionized water. While leaching did not affect the sorption of metals in columns which had been perfused with aqueous solvents, sorption behavior of metals changed significantly in columns which had been perfused with alcohol solvents. Leaching caused desorption of 5 to 30% of the sorbed Ni. In general, Cd was desorbed (up to 45%) from the soils tested. The exceptions were River Sand columns perfused with diethylene and triethylene glycol in which additional Cd was sorbed to the soil from the soil solution. Additional Zn was sorbed in all columns tested with the exception of the Canelo I column perfused with ethyl alcohol.

Miller, R. M., Singer, G. M., Rosen, J. D., & Bartha, R. (1988). Photolysis primes biodegradation of benzo[a]pyrene. Applied and Environmental Microbiology, 54(7), 1724-1730.

PMID: 3415236;PMCID: PMC202736;Abstract:

14C-labeled benzo[a]pyrene (BaP) was used as a model compound for polycyclic aromatic hydrocarbons (PAH) in order to assess the effect of photolytic pretreatment on the subsequent fate of BaP in sewage sludge and soil test systems. Photolysis was performed in methanolic solution with or without 0.1 M H2O2, under either UV light (300 nm) or natural sunlight. The presence of H2O2 greatly enhanced the rate of photolysis both with UV and with natural sunlight. Intact BaP resisted biodegradation in both test systems. Photolysis transformed BaP to polar materials that were subject to increased mineralization and binding in both biological test systems. As shown by the Ames assay, photolysis decreased the mutagenicity of BaP to test strains TA98 and TA104 only moderately. The photolysate had an increased acute toxicity and lost its need for activation by S-9 enzymes. However, during subsequent incubation in soil or sewage sludge, mutagenicity decreased rapidly by one to two orders of magnitude and acute toxicity disappeared due to the mineralization and binding of photoproducts to humic materials. Photolysis of BaP and similar PAH compounds represents a useful treatment option that could be applied to certain PAH-containing petroleum refinery sludge and to coal tar residues in order to facilitate their detoxification and environmentally safe disposal.