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Bioavailability
of Arsenic to Edible Plants Grown in Poultry Litter
Applied Soils
Jennifer
Parker, Research Associate, Frontier Geosciences, 414
Pontius Ave. N, Seattle, WA 98109, Tel: 206-622-6960, Fax:
206-622-6870, Email: jennp@FrontierGeosciences.com
Nicolas Bloom, Senior Research Scientist, Frontier
Geosciences, 414 Pontius Ave. N, Seattle, WA 98109, Tel:
206-622-6960
Hakan Gürleyük, Ph.D., Research Scientist, Frontier
Geosciences, 414 Pontius Ave. N, Seattle, WA 98109, Tel:
206-622-6960
The
poultry industry is one of the largest and fastest growing
livestock production systems in the world. Poultry is often treated with organo-arsenical feed additives
used to control coccidial intestinal parasites, improve
feed efficiency, and promote rapid weight gain. Since
these arsenic compounds are not readily absorbed by
poultry, poultry litter may contain as much as 30-50 mg As
kg-1. Approximately, 90% of the 13 million
metric tons of poultry litter annually produced in the
U.S. is applied as a fertilizer on cropland and pasture.
There are already reports of high inorganic arsenic
concentrations in rivers close to these chicken farms and
chicken litter applied fields during/after storm events.
Another important but unstudied aspect of this application
is the possible accumulation of arsenic in agricultural
plants. This study focuses on the bioavailability of As to
various edible plants grown in soils amended with poultry
litter. Arsenic speciation changes in the soil and plants
over time was also monitored. For comparison, soils were
also amended with inorganic As species and differences in
plant bioavailability was assessed. In addition, we
evaluated the ability of different leach solutions to
target the desired As species, as well as a variety of
chemical soil extractions to determine their usefulness in
predicting plant bioavailable As in soils. Arsenic
speciation was conducted using both ion chromatography -
inductively coupled mass spectrometry (IC-ICP-MS) and
hydride generation - cryogenic trapping - atomic
absorption spectroscopy (HG-CT-AAS).
Determination
of Inorganic Arsenic in Soils, Surface Waters and Plants
in Old Mining Sites of Maldon, Australia
Khawar
Sultan and Kim Dowling, School of Science and Engineering,
University of Ballarat, Mt. Helen, Vic 3353, Australia
Arsenic
concentrations in surface water, plant and soil (< 2 mm
fraction) samples were collected from six different sites
located in area that had been affected due to mining,
smelter activities and natural enrichment due to
geological mineralization. Concentrations in excess of
1000 mg/kg of arsenic has been recorded in topsoils (0-10
cm) and more than 51% of soil samples reported
concentrations >500 mg/kg. Concentrations of As in
freshwater at sites exceeded permissible limits even
though atmospheric contribution is less significant during
the past decades. Total arsenic concentration in all soil
samples were higher than those found at non-contaminated
sites particularly at State Battery location which
recorded extreme level of 3265 mg/kg of As. The total
arsenic concentrations of various plants were in the range
~ 0.18-6.9 mg/kg of As (dry mass) and was observed
bioavailable; with difference depending on site location
and possibly plant species.
The
Maldon mining district has been mined for years for gold
and has resulted in waste rock and tailings, rich in
sulphides, over an area including the city itself.
Oxidation of these sulphides result in mobility of As and
other heavy metals into runoff and drains into local
drainage tributaries and water bodies, which ultimately
may contaminate groundwater. Wide range of pH (3.8 ~ 8.3)
and Eh (-286 ~ +396 mV) has been measured in surface
waters. Total dissolved inorganic As in surface waters was
measured as high as 11.5 mg/l in acidified mine drainage
and possible adsorption on to Fe oxides is taking place
preventing extreme mobility. Plants growing on these sites
were shown to accumulate arsenic to levels as high as 6.9
mg/kg of As. Elevated As concentrations in soils, waters
and plants may also have originated from natural source
partly but strong indications by high concentration in
particular sites due to mining activity was observed
clearly.
The
current work focused on identification of localized
contamination of As and its possible mobility and
bioavailability. This study can be useful to examine the
measures to prevent the mobilization of the contaminant
source material in future.
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