Biomedical subjects

J M Arocena

Publications and source records attributed to J M Arocena.

4 recordsLinked to original sources

PubMed2005

Properties of hydrocarbon- and salt-contaminated flare pit soils in northeastern British Columbia (Canada).

Many contaminated sites in Canada are associated with flare pits generated during past petroleum extraction operations. Flare pits are located adjacent to well sites, compressor stations and batteries and are often subjected to the disposal of wastes from the flaring of gas, liquid hydrocarbons and brine water. This study was conducted to evaluate the physical, chemical, electrical and mineral properties of three flare pit soils as compared to adjacent control soils. Results showed that particle size distribution, pH, total N, cation exchange capacity, exchangeable Mg(2+), and sodium adsorption ratio were similar in soils from flare pits and control sites. Total C, exchangeable Ca(2+), K(+) and Na(+), soluble Ca(2+), Mg(2+), K(+) and Na(+) and electrical conductivity were higher in flare pit soils compared to control soils. X-ray diffraction and scanning electron microscopic analyses showed the presence of gypsum [CaSO(4).2H(2)O], dolomite [CaMg(CO(3))(2)], pyrite [FeS(2)], jarosite [KFe(3)(OH)(6)(SO(4))(2)], magnesium sulphate, oxides of copper and iron+copper in salt efflorescence observed in flare pit soils. Soils from both flare pits and control sites contained mica, kaolonite and 2:1 expanding clays. The salt-rich materials altered the ionic equilibria in the flare pit soils; K(Mg-Ca) selectivity coefficients in control soils were higher compared to contaminated soils. The properties of soils (e.g., high electrical conductivity) affected by inputs associated with oil and gas operations might render flare pit soils less conducive to the establishment and growth of common agricultural crops and forest trees.

British Columbia↗

PubMed2005

Uptake, distribution, and speciation of chromium in Brassica juncea.

Brassica juncea (Indian mustard) has been widely used in phytoremediation because of its capacity to accumulate high levels of chromium (Cr) and other metals. The present study was conducted to investigate mechanism(s) involved in Cr binding and sequestration by B. juncea. The plants were grown under greenhouse conditions in field-moist or air-dried soils, amended with 100 mg kg(-1) of Cr (III) or VI). The plant concentrated Cr mainly in the roots. B. juncea removed an average of 48 and 58 microg Cr per plant from Cr (III) and Cr (VI)-treated soils, respectively. The uptake of Cr was not affected by the moisture status of the soils. X-ray absorption near-edge spectroscopy measurements showed only Cr (III) bound predominantly to formate and acetate ligands, in the bulk and rhizosphere soils, respectively. In the plant tissues, Cr (III) was detected, primarily as acetate in the roots and oxalate in the leaves. X-ray microprobe showed the sites of Cr localization, and probably sequestration, in epidermal and cortical cells in the roots and epidermal and spongy mesophyll cells in the leaves. These findings demonstrate the ability of B. juncea to detoxify more toxic Cr (VI), thereby making this plant a potential candidate for phytostabilization.

Brassica↗

PubMed2001

Evaluation of iron-phosphate as a source of internal lake phosphorus loadings.

Biological, physical and chemical characteristics of the water column of a shallow (Zmax = 9.2 m), small (surface area 3.8 km2) residential and recreational lake near Prince George, British Columbia, indicated that the system was being loaded internally with phosphorus (P) from the sediments. The abundance of P released from the fine glaciolacustrine, and organic rich sediments was resulting in excess algal and weed growth. It was postulated that iron-phosphate reduction at redox potentials below approximately 200 mV and/or bacterially mediated orthophosphate (PO4-P) releases could be occurring. The development of an appropriate nutrient management strategy required that the process associated with the sediment P release be determined. The MINTEQA2 geochemical model was used to predict the release of orthophosphate (PO4-P) into the interstitial water with the assumption that P is present alternately as strengite, variscite and hydroxyapatite. The predicted release of PO4-P from these P containing minerals was compared to the concentration of PO4-P and total phosphorus (TP) in the overlying hypolimnion. In order to improve the accuracy of the model prediction, the proportion of the sediment present as iron-bound phosphate was estimated. A significant correlation between the observed hypolimnetic TP and interstitial PO4-P concentrations as predicted from iron-bound P dissolution (r2 = 0.59) was found. Total phosphorus release rates to the hypolimnion were also found to be strongly correlated to the iron-bound P component of the sediment (r2 = 0.88). Multivariate regression analyses showed significant relationships between hypolimnetic PO4-P and sediment iron-bound P, Eh, and interstitial Fe (r2 = 0.76). These results provided sufficient evidence to conclude that PO4-P in the system is predominantly bound to Fe-containing minerals and therefore could be managed using treatment techniques that address iron-bound phosphates.

Environmental Monitoring↗

PubMed1995

Radon emanation coefficients for phosphogypsum.

Phosphogypsum is a by-product of the phosphate fertilizer industry which is stockpiled in large quantities world-wide. Phosphogypsum consists mainly of dihydrate gypsum (CaSO42H2O) but also contains elevated concentrations of 226Ra and other inorganic species which originate from the processing of phosphate rock. 222Rn gas is the first decay product of 226Ra and has been identified as one of the major environmental concerns associated with phosphogypsum. This study was conducted to determine effects of particle size, weathering, and moisture content on the 222Rn emanation coefficient (epsilon) for phosphogypsum. Average epsilon for air-dry, unfractionated phosphogypsums derived from Togo, Florida, or Idaho rock was approximately 12%. Average epsilon for fine fraction phosphogypsum (< 20 microns diameter) was greater than for unfractionated phosphogypsum by a factor of 4.6, 1.4, and 4.4 for samples derived from Idaho rock, Togo rock, and Florida rock, respectively. Phosphogypsum samples subjected to an artificial weathering procedure lost 40% mass, with no change in epsilon. Increasing water content was found to first slightly decrease, then to increase epsilon compared to air-dry samples; epsilon for 100% saturated phosphogypsum was 1.9-fold greater than in air-dry phosphogypsum. Particle size sorting could account for variability of 222Rn exhalation at repositories. Very high moisture contents could slightly increase 222Rn emanation, but exhalation would likely be reduced due to slow diffusion through porosity of saturated phosphogypsum.

Calcium Sulfate↗