Phytodegradation of organic compounds.

Abstract

The phytodegradation of organic compounds can take place inside the plant or within the rhizosphere of the plant. Many different compounds and classes of compounds can be removed from the environment by this method, including solvents in groundwater, petroleum and aromatic compounds in soils, and volatile compounds in the air. Although still a relatively new area of research, there are many laboratories studying the underlying science necessary for a wide range of applications for plant-based remediation of organic contaminants.

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Phytodegradation of organic compounds
Lee A Newman1,2?and Charles M Reynolds3
The phytodegradation of organic compounds can take place
inside the plant or within the rhizosphere of the plant. Many
different compounds and classes of compounds can be
removed from the environment by this method, including
solvents in groundwater, petroleum and aromatic compounds
in soils, and volatile compounds in the air. Although still a
relatively new area of research, there are many laboratories
studying the underlying science necessary for a wide range
of applications for plant-based remediation of organic
contaminants.
Addresses
1University of South Carolina Arnold School of Public Health, 800 Sumter
Street, Columbia, SC 29208, USA
2The Savannah River Ecology Laboratory Aiken, SC 29208, USA
3US Army Engineer Research Development Center, Cold Regions
Research and Engineering Laboratory, 72 Lyme Road, Hanover,
NH 03755-1290, USA
?e-mail: Newman2@gwm.sc.edu
Current Opinion in Biotechnology 2004, 15:225–230
This review comes from a themed issue on
Environmental biotechnology
Edited by Michael Y Galperin and Alan JM Baker
Available online 8th May 2004
0958-1669/$ – see front matter
? 2004 Elsevier Ltd. All rights reserved.
DOI 10.1016/j.copbio.2004.04.006
Abbreviations
MTBE
PAH
PCB
TCE
TNT
TPH
methyl-tert-butyl ether
polycyclic aromatic hydrocarbons
polychlorinated biphenyl
trichloroethylene
2,4,6-trinitrotoluene
total petroleum hydrocarbon
Introduction
Phytoremediation is the use of plants to remediate con-
taminants in the environment. With the high costs of site
remediation, it is important that we continue to develop
and refine innovative, low-cost methods for cleaning the
environment. Phytoremediation also has the benefit of
contributing to site restoration when remedial action is
ongoing. The phytoremediation of organic compounds
can take place from the soil, air, groundwater or surface
water. The action of plants can include the degradation,
adsorption, accumulationandvolatilization ofcompounds
or the enhancement of soil rhizosphere activity. Which
plant activity occurs can depend not only on the medium
to be remediated and the type of plant used, but also on
the physical properties of the contaminant. Thus, two
different compounds in the same medium can interact
with a plant in very different ways. In this review, we
classify compounds of a similar nature together and dis-
cuss how recent studies have helped to elucidate plant
interactions with those compounds.
A summary of the contaminants and plants discussed is
given in Table 1.
Phytoremediation of solvents
Thephytoremediationofsolventsisalmost atthe pointof
being considered an accepted technology, even as new
information on the fate of solvents in plants continues to
come to light. Shang and Gordon [1] showed that the
groundwater contaminant trichloroethylene (TCE) taken
up by suspension cell cultures of hybrid poplar becomes
part of the non-volatile, un-extractable portion of the
cells. In whole plant studies, however, Ma and Burken
[2??] demonstrated that the stems and trunks of plants
releaseTCEtotheatmosphere.Tobetterunderstandthe
fate of TCE in whole plant systems, one of us (Newman)
is collaborating with Burken to better define the mass
balance and determine all fates of TCE in plants.
Other groundwater contaminants also continue to be
studied. Ma and Burken [3] looked at the diffusion of
compounds such as 1,1,2,2-tetrachloroethane and carbon
tetrachloride from the transpiration stream of mature
trees on contaminated sites and found that stem concen-
trations can be used as indicators of aquifer concentra-
tions. The fate of ethylene dibromide (EDB) and TCE
has also been studied in the tropical tree Leuceana leuco-
cephala [4] and the plant was shown to be highly effective
at taking up both compounds. Bromide levels in the
hydroponic solutions of plants exposed to EDB showed
a marked increase, indicating a dehalogenation activity in
the plants. Laboratory studies with a hairy root culture of
Brassica napus exposed to 2,4-dichlorophenol resulted in
greater than 90% removal of the compound from solution
over a range of pH values [5]. The plant-based treatment
of benzotriazoles, corrosion inhibitors used in glycol-
based deicing fluids, has also been studied. Castro et al.
[6] observed that benzotriazoles appeared to be actively
taken up and then incorporated into plant tissue by sun-
flowers (Helianthus annuus) grown in hydroponic solution.
Advances in the phytoremediation of methyl-tert-butyl
ether (MTBE) have progressed more slowly. Although
previous studies have shown that a wide variety of plants
are capable of taking up the compound, little is known
about its fate. Trapp et al. [7] looked at the fate of MTBE
in a variety of plants including trees, grasses and herbs,
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and found no evidence for its metabolism by the plants;
they proposed that volatilization was the main fate. It was
also shown by Ramaswami et al. [8] that rhizosphere
bacteria were not a significant source of MTBE degrada-
tion. In laboratory studies, Ma et al. [9] found that not only
wasMTBEreleasedfromtheleaves,asreportedinseveral
previous studies, but it also diffused from the trunk of the
plants. A morerecent studyof fivemature Montereypines
exposed to MTBE in the aquifer reported much higher
levels of tert-butyl alcohol (TBA) than MTBE through
the transpiration stream, indicating that metabolism was
taking place either in the rhizosphere or within the
plant system [10??]. This study also showed a significant
decrease in MTBE levels in the aquifer as it passed under
the trees, indicating that phytoremediation may be a
viable option forMTBE, even if thefateof thecompound
in the plant is not yet fully understood.
Phytoremediation of pesticides
The area of pesticide phytoremediation has recently
yielded some interesting results. Li et al. [11] looked
at the uptake of trifluralin and lindane by ryegrass:
trifluralin appeared to be metabolized by the plant,
whereas lindane had minimal metabolism and instead
formed bound residues. A number of factors have been
shown to effect the phytoremediation of pesticides. For
example, White and colleagues [12,13??] showed that
organic acids increased the uptake of 2,2-bis(p-chloro-
phenyl)-1,1-dichlorethylene (DDE) and Knuteson et al.
[14] reported that younger plants (two weeks old) exhib-
ited greater uptake of simazine (2-chloro-4,6-bis(ethyla-
mino)-1,3,5-triazine) than plants that were just two
weeks older. Although it has long been known that the
abilitytotakeupandtranslocateheavymetalsisnotonly
species-specific, but also ecotype specific, White and
coworkers [15??,16] reported that the uptake of DDE
was also subspecies specific, with certain cultivars show-
ingsignificantlyhigheruptake.Theyconcludedthatthis
difference was the result of higher exudation rates of low
molecular weight organic acids.
Phytoremediation of explosive compounds
Thephytoremediationofexplosivecompoundsisofgreat
interest to the Department of Defense, as they look for
innovative technologies to reduce the levels of contami-
nants onranges while still keeping the ranges operational.
In this regard, Wang et al. [17] studied the interactions
between 2,4,6-trinitrotoluene (TNT) and Myriophyllum
aquaticum, looking at transformation rates. Planting with
Johnsongrass or wild ryegrass has been shown to decrease
soil concentrations of TNT [18] and it has been reported
that the use of plants to remediate surface waters con-
taminated with TNT could reduce toxicity in the system
[19]. A newly discovered endophytic bacterium, Methylo-
bacterium sp. (isolated from hybrid poplar), was shown by
van Aken et al. [20??] to be capable of degrading TNT,
Table 1
Summary of contaminants and plants discussed in the text*.
ClassContaminant Plants studiedEffect studied
ChlorinatedTCEPoplarMetabolism [1],
volatilization from trunk [2??]
Volatilization from trunk
Metabolism
Metabolism
Metabolism
Metabolism
Volatilization from trunk
Metabolism
Uptake
Uptake
Uptake [14]
Metabolism
Metabolism
Metabolism
Metabolism
Rhizosphere effects
CT, tetrachloroethane
TCE
2,4-Dichlorophenol
Benzotriazoles
MTBE
MTBE
EDB
Trifluralin, lindane
DDE
Simazine
TNT
HMX
TNT, RDX, HMX
Perchlorate
Poplar [3]
Leuceana [4], poplar rhizosphere [26]
Brassica [5]
Hellianthus [6]
Herbaceous plants [7], pine [10??]
Poplar [9]
Leuceana [4]
Rye [11]
Curcurbita [12,13??,15??,16]
Parrot feather, canna
Parrot feather [18], Arabidopsis [21]
Poplar [22], bean, alfalfa, canola [23]
Poplar endophytes
Tobacco [24], poplar [25]
Sorghum [27], alfalfa [39], clover, rye [40],
poplar [42,43], willow [44]
Rye [28], fescue [30??], Kandelia [42], Bruguiera [47]
Pothos [48]
Fescue [33]
Poplar [42,43]
Willow [44]
Grasses native to California (US) [35]
Brassica [41]
De-icing agents
Gasoline additivies
Pesticides
Energetics
PAH/TPH
Pyrene
Gasoline
Jet fuel
TPH
Mineral oil
Diesel, heavy oil
Rhizosphere effects
Atmospheric remediation
Rhizosphere effects
Rhizosphere effects
Rhizosphere effects
Rhizosphere effects
Rhizosphere effectsPCBs
*This does not reflect what was done in previous studies and should not be considered an inclusive list of all plant and contaminants studied.
CT, carbon tetrachloride; DDE, 2,2-bis(p-chlorophenyl)-1,1-dichlorethylene; EDB, ethylene dibromide; HMX, octahydro-1,3,5,7-tetranitro-
1,3,5-tetrazocine; RDX, hexahydro-1,3,5-trinitro-1,3,5-triazine.
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hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), and octa-
hydro-1,3,5,7-tetranitro-1,3,5-tetrazocine (HMX); it may
be that this bacterium has a major role in the degradation
of explosive compounds in plants. However, Ekman et al.
[21] found that the detoxification enzymes cytochrome
P450, glutathione S-transferase, an ABC transporter, and
a probable nitroreductase were all induced in Arabidopsis
roots following TNT exposure, which opens the possi-
bility of these enzymes being involved in plant degrada-
tion of TNT. In contrast to the promising results seen
with TNT, Yoon et al. [22] showed that HMX has limited
metabolism in plants, and could result in accumulation
of the compound in plants. Likewise, Groom et al. [23]
looked at HMX uptake using alfalfa (Medicago sativa),
bush bean (Phaseolus vulgaris), canola (Brassica rapa), and
other plants and saw the same limited uptake and meta-
bolism in the plants, suggesting reduced potential for the
phytoremediation of this compound.
Diverse results have also been observed for the remedia-
tion of perchlorate. Although one study reported the
accumulation of perchlorate in the leaves of tobacco
plants [24] another showed that poplars were able to
reduce perchlorate, albeit at a low level [25].
Phytoremediation of petroleum compounds
The rhizosphere degradation of chlorinated solvents
under new plantations is limited, but work by Godsy
et al. [26] indicates that as the trees age the microbial
populations might change and foster anaerobic degrada-
tion. With compounds such as the polycyclic aromatic
hydrocarbons (PAHs), petroleum compounds and poly-
chlorinated biphenyls (PCBs), the role of the rhizosphere
is much more critical.
Efforts to demonstrate plant or rhizosphere effects on
petroleum degradation, particularly PAHs, continue. In a
greenhouse study, Banks et al. [27] observed generally
greater remediation efficiency in soil planted with four
genotypes of Sorghum bicolor (L.) compared with unve-
getated controls. Although the genotypes were selected
for different root characteristics and root exudate levels,
these differences were not reflected in remediation effi-
ciencies. Measuring plant effects on PAH degradation in
soil remains difficult, and our ability to measure phyto-
remediation treatment effects is confronted by numerous
interactions among the soil-rhizosphere-microbial-plant
system. Parts of the system interact on a continuous basis,
interactions vary with conditions, such as moisture and
temperature, as well as with the growth stage of both
plants and microorganisms. These interactions make
understanding and monitoring phytoremediation com-
plex. Results from studies are mixed. Using small field
plotsinpreviouslyvegetatedsoilsthathadbeenamended
with pyrene, mixed and then either revegetated with
annual ryegrass (Lolium multiflorum Lam.) or kept fallow,
Lalande et al. [28] reported greater pyrene loss from
unvegetated treatments and suggested that microorgan-
isms may use easily degradable organic matter as a carbon
source rather than pyrene. Joner et al. [29] suggested that
priming effects associated with experimental protocols
were large, and may tend to mask beneficial effects from
the synergistic effects of fertilizing and planting. Solid
evidence for increased degradation with plants continues
to be reported. Using14C-labeled pyrene, Chen et al.
[30??] showed 38% and 30% pyrene mineralization in tall
fescue (Festuca arundinacea) and switchgrass (Panicum
virgatum L.), respectively, compared with 4.3% in the
unplanted control.
Contamination
affects the carbon:nitrogen (C:N) ratio in soil and can
lead to nitrogen immobilization. Adam and Duncan [31]
evaluated leguminous plants in diesel-contaminated soil
and found that contaminated soil had fewer nodules, but
that these nodules were more developed. White et al. [32]
investigated soil amendments with different C:N ratios
for their effects on both seed germination and plant
growth. Addition of boiler litter, which had a C:N ratio
of approximately eight, resulted in lower soil total pet-
roleum hydrocarbons (TPHs) compared to amendments
with higher C:N ratios.
withhydrocarbon-basedcompounds
In field soils, numerous soil–plant interactions and soil
conditions, including soil moisture and temperature, may
influence contaminant fate. Plants can affect soil water
content and movement in several ways. Karthikeyan et al.
[33] used column studies to demonstrate that transport
and biodegradation of jet fuel (JP-8) were affected by soil
water, and that soil columns planted with fescue grass
(Festuca arundinacia) had less leaching of JP-8. They
suggested that plant transpiration and associated water
movement could favor biodegradation by keeping mobile
contaminants near the soil surface, and they developed a
modeling approach to describe water and JP-8 transport
[34] (Table 1).
Although field studies are more difficult to conduct and
monitor than greenhouse studies, results are encouraging.
Banks etal.[35] foundthat vegetative treatmentofdiesel-
and heavy-oil-contaminated soil yielded both lower TPH
values in the vegetated soil and reduced toxicity. They
suggested that longer term treatment may be needed for
further reductions in TPH concentration. Robson et al.
[36]haveprovidedalistofplantsadaptedtohydrocarbon-
contaminated soils and cold regions.
Our understanding of rhizosphere microbiology and its
changes during phytoremediation is improving. Siciliano
et al.[37??] observed greater levels of hydrocarbon-related
catabolic genes (ndoB, alkB and xylE) in rhizosphere soils
relative tobulk soil.Muratova etal.[38] used fluorescence
microscopy to show that the microflora in the rhizosphere
of bitumen-contaminated soil was greater than in
Phytodegradation of organic compounds Newman and Reynolds 227
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unplanted soil, and that the community structure was also
different. Differences between alfalfa (Medicago sativa)
and reed (Phragmites australis) rhizospheres were also
observed. Additionally, alfalfa enhanced the PAH-
degrading population in the rhizosphere [39]. In a pot
study, Joner and Leyval [40] found that in PAH-contami-
nated soil planted with a clover–ryegrass mix PAH con-
centrations decreased as a function of proximity to the
roots, and that mycorrhiza generally enhanced plant
growth and favored growth of clover at the expense of
ryegrass. Singer et al. [41] repeatedly augmented Aro-
chlor1242-contaminated soil with PCB-degrading bac-
teria, carvone and salicyic acid as enzyme inducers, a
surfactant and minimal salts medium, and compared
Brassica nigra to non-vegetated controls. The B. nigra-
planted treatments resulted in 61% PCB removal in the
top 6 cm after nine weeks of bioaugmentation, compared
with 43% and 14% PCB removal in the 0–2 and 2–6 cm
depths, respectively, in unplanted controls.
In addition to grasses and legumes, trees such as Populus
are increasingly being considered for use in PAH and
TPH degradation. In short-term tests, Wittig and collea-
gues [42,43] found that poplar cuttings grown in a PAH-
amended sand-nutrient solution had similar shoot bio-
mass, growth and leaf water content to the controls, but
that transpiration, nutrient solution uptake, and root mass
werereduced. Thewatercontentoftheleaveswassimilar
among plants from the PAH-contaminated soils and con-
trols. The effects were also dependent on the PAH under
study. Willow (Salix viminalis L. ‘Orm’) has been eval-
uated for the dissipation of mineral oil and PAHs in
dredgedsediment[44].
decreased 57% after 1.5 years in the willow-planted
treatment compared to 15% in the control. In the vege-
tated soil, mineral oil degradation was greater in the roots
zone than in the total column of soil.
Mineral oil concentration
Because the volume of soil affected by rhizosphere pro-
cesses is related to root morphology and size, there is
continued interest in rooting patterns. Rentz et al. [45??]
investigated five passive methods for increasing oxygen
delivery to enhance root development and plant growth.
Using commercial oxygen release compounds stimulated
plantgrowthandrootdensityinapotstudy.Theseresults
suggest that there may be effective ways to enhance root
growth in oxygen-limiting situations and to couple phy-
toremediation with other technologies to enhance both.
Ke etal.[46] investigatedusing mangrove (Kandelia candel
and Bruguiera gymnorrhiza) wetland systems to treat pyr-
ene-contaminated sediments. After six months, pyrene
concentrations decreased in the mangrove treatments
relative to the controls. Although there was a measurable
increase in pyrene concentrations in the roots relative to
the non-pyrene control roots, the increase was minor
compared with the total pyrene removed from the sedi-
ment, suggesting that plant uptake was not a significant
path for pyrene loss. The authors found that adding
humic acid (HA) to the soil reduced both plant growth
andpyreneloss,suggestingthatpyrenebindingtotheHA
limited its bioavailability [47].
Although most problems with petroleum compounds are
associated with contaminated soils and groundwater, the
atmospheric release of gasoline compounds also needs to
be addressed. Oyabu et al. [48] investigated the ability of
Epipremnum aureum (golden pothos) to remove gasoline
from the air and found that the plants purification ability
reached a maximum value 40 h after gasoline vapors were
inroduced into the growth chamber. The authors did not
separate soil effects from plant effects in their study.
Models of phytoremediation
Difficultiesinmeasuringphytoremediationrates,predict-
ing treatment times, and developing monitoring schemes
are recognized as current limitations to using phytoreme-
diation. Developing effective models may help to address
these limitations and might help the research community
to understand the interactions among the many processes
that contribute to phytoremediation. Thoma and collea-
gues [49,50] developed a model for screening grass spe-
cies for the phytoremediation of weathered petroleum.
Models for calculating hydraulic control based on tran-
spiration and groundwater characteristics have been dis-
cussed and evaluated, with the suggestion that field
measurements be used to verify model predictions when-
ever possible [51]. International interest in using phytor-
emediation has lead to reviews that discuss both models
and processes thought to be important [52], as well as
performance evaluations of existing models against
experimental datasets [53]. Matthews et al. [54] used a
numerical groundwater flow model and evaluated how
variations in hydrogeologic and seasonal growth para-
meters influenced the minimum plantation area needed
for plume capture. They found that the aquifer horizontal
hydraulic conductivity and saturated thickness directly
influenced the plantation size.
Conclusions
Reviews and conference summaries of phytoremediation
studiesareappearingregularlyandallowconciseoverviews
ofinternationalphytoremediationefforts [55–63]. As more
researchers, site owners and regulators become aware of
thetechnology,thereisagreatpotentialfortheapplication
ofthisareaofphytoremediation.Advancesingroundwater
and soil remediation continue to lead to a better under-
standingof themany processes by which plants canhave a
positive impact on contamination in the environment.
Acknowledgements
The authors gratefully acknowledge the efforts of SE Hardy and support
from the US Army Environmental Quality Basic Research Program, the
Department of Energy and the US-NIEHS, grant P42 ES04696, in
developing this review.
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References and recommended reading
Papers of particular interest, published within the annual period of
review, have been highlighted as:
? of special interest
??of outstanding interest
Shang TQ, Gordon MP: Transformation of [14C]
trichloroethylene by poplar suspension cells. Chemosphere
2002, 47:957-962.
1.
2.
??
The authors showed that the trunks of trees can act as a portal for the
diffusion of TCE out of the plant and into the surrounding atmosphere.
Ma X, Burken JG: TCE diffusion to the atmosphere in
phytoremediation applications. Environ Sci Technol 2003,
37:2534-2539. [Comment in 37:310A].
3. Ma X, Burken JG: VOCs fate and partitioning in vegetation:
use of tree cores in groundwater analysis. Environ Sci Technol
2002, 36:4663-4668. [Erratum published in Environ Sci Technol
37:2024].
4.Doty SL, Shang TQ, Wilson AM, Moore AL, Newman LA, Strand SE,
Gordon MP: Metabolism of the soil and groundwater
contaminants, ethylene dibromide and trichloroethylene,
by the tropical leguminous tree, Leuceana leucocephala.
Water Res 2003, 37:441-449.
5.Agostini E, Coniglio MS, Milrad SR, Tigier HA, Giulietti AM:
Phytoremediation of 2,4-dichlorophenol by Brassica napus
hairy root cultures. Biotechnol Appl Biochem 2003, 37:139-144.
6.Castro S, Davis LC, Erickson LE: Phytotransformation of
benzotriazoles. Int J Phytoremed 2003, 5:245-266.
7. Trapp S, Yu X, Mosbaek H: Persistence of methyl tertiary butyl
ether (MTBE) against metabolism by Danish vegetation.
Environ Sci Pollut Res Int 2003, 10:357-360.
8.Ramaswami A, Rubin E, Bonola S: Non-significance of
rhizosphere degradation during phytoremediation of MTBE.
Int J Phytoremed 2003, 5:315-332.
9.Ma X, Andrew AR, Burken JG, Albers S: Phytoremediation of
MTBE with hybrid poplar trees. Int J Phytoremed in press.
10.
??
Newman LA, Arnold CW: Phytoremediation of MTBE – a review
of the state of the technology. In MTBE Remediation Handbook.
Edited by Moyer EE, Kostecki PT. Amherst, Massachusetts:
Amherst Scientific Publishers; 2003:279-288.
Although a review article, this was also the first publication of data from a
fieldsitedemonstrating thepotential for treestohaveapositive impacton
an MTBE-contaminated aquifer.
11. Li H, Sheng G, Sheng W, Xu O: Uptake of trifluralin and lindane
from water by ryegrass. Chemosphere 2002, 48:335-341.
12. White JC, Kottler BD: Citrate-mediated increase in the uptake of
weathered 2,2-bis(p-chlorophenyl) 1,1-dichloroethylene
residues by plants. Environ Toxicol Chem 2002, 21:550-556.
13.
??
White JC, Mattina MI, Lee WY, Eitzer BD, Iannucci-Berger W: Role
of organic acids in enhancing the desorption and uptake of
weathered p,p(-DDE by Cucurbita pepo. Environ Pollut 2003,
124:71-80.
In this and related papers, the authors begin to unravel relationships
among root exudates and contaminant fate processes.
14. Knuteson SL, Whitwell T, Klaine SJ: Influence of plant age and
size on simazine toxicity and uptake. J Environ Qual 2002,
31:2096-2103.
15.
??
White JC, Wang X, Gent MP, Iannucci-Berger W, Eitzer BD,
Schultes NP, Arienzo M, Mattina MI:Subspecies-level variation in
the phytoextraction of weathered p,p(-DDE by Cucurbita pepo.
Environ Sci Technol 2003, 37:4368-4373.
The authors demonstrate what has been seen for many years in the study
of metal uptake: that differences in varieties within the same species can
be a large factor in plant uptake of organic compounds.
16. White JC: Differential bioavailability of field-weathered
p,p(-DDE to plants of the Cucurbita and Cucumis genera.
Chemosphere 2002, 49:143-152.
17. WangC,LyonDY,HughesJB,BennettGN:Roleofhydroxylamine
intermediates in the phytotransformation of 2,4,6-
trinitrotoluene by Myriophyllum aquaticum. Environ Sci Technol
2003, 37:3595-3600.
18. Sung K, Munster CL, Rhykerd R, Drew MC, Corapcioglu MY:
The use of vegetation to remediate soil freshly
contaminated by recalcitrant contaminants. Water Res 2003,
37:2408-2418.
19. Hitchcock DR, McCutcheon SC, Smith MC: Using rotifer
population demographic parameters to assess impacts of the
degradation products from trinitrotoluene phytoremediation.
Ecotoxicol Environ Saf 2003, 55:143-151.
20.
??
van Aken B, Yoon JM, Schnoor JL: Biodegradation of nitro-
substituted explosives 2,4,6-trinitrotoluene, hexahydro-1,3,5-
trinitro-1,3,5-triazine, and octahydro-1,3,5,7-tetranitro-1,3,5-
tetrazocine by a phytosymbiotic Methylobacterium
sp. associated with poplar tissues (Populus deltoides x nigra
DN34). Appl Environ Microbiol 2004, 70:508-517.
The authors show that for some explosive compounds degradation may
be through plant vascular tissue endophytes, rather than through plant
metabolic pathways.
21. Ekman DR, Lorenz WW, Przybyla AE, Wolfe NL, Dean JF: SAGE
analysis of transcriptome responses in Arabidopsis roots
exposed to 2,4,6-trinitrotoluene. Plant Physiol 2003,
133:1397-1406.
22. Yoon JM, Oh BT, Just CL, Schnoor JL: Uptake and leaching of
octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine by hybrid
poplar trees. Environ Sci Technol 2002, 36:4649-4655.
23. Groom CA, Halasz A, Paquet L, Morris N, Olivier L, Dubois C,
Hawari J: Accumulation of HMX (octahydro-1,3,5,7-tetranitro-
1,3,5,7-tetrazocine)inindigenousandagriculturalplantsgrown
in HMX-contaminated anti-tank firing-range soil. Environ Sci
Technol 2002, 36:112-118.
24. Sundberg SE, Ellington JJ, Evans JJ, Keys DA, Fisher JW:
Accumulation ofperchlorateintobacco plants:developmentof
a plant kinetic model. J Environ Monit 2003, 5:505-512.
25. van Aken B, Schnoor JL: Evidence of perchlorate (ClO4S)
reduction in plant tissues (poplar tree) using radio-labeled
36ClO4?. Environ Sci Technol 2002, 36:2783-2788.
26. Godsy EM, Warren E, Paganelli VV: The role of microbial
reductive dechlorination of TCE at a phytoremediation site.
Int J Phytoremed 2003, 5:73-88.
27. Banks MK, Kulakow P, Schwab AP, Chen Z, Rathbone K:
Degradation of crude oil in the rhizosphere of sorghum bicolor.
Int J Phytoremed 2003, 5:225-234.
28. Lalande TL, Skipper HD, Wolf DC, Reynolds CM, Freedman DL,
Pinkerton BW, Hartel PG, Grimes LW: Phytoremediation of
pyrene in a cecil soil under field conditions. Int J Phytoremed
2003, 5:1-12.
29. Joner EJ, Hirmann D, Szolar OH, Todorovic D, Leyval C,
LoibnerAP:PrimingeffectsonPAHdegradationandecotoxicity
during a phytoremediation experiment. Environ Pollut 2004,
128:429-435.
30.
??
Chen YC, Banks MK, Schwab AP: Pyrene degradation in the
rhizosphere of tall fescue (Festuca arundinacea) and
switchgrass (Panicum virgatum L.). Environ Sci Technol 2003,
37:5778-5782.
The authors provide data based on14C techniques that show a clear
phytoremediation effect.
31. Adam G, Duncan H: The effect of diesel fuel on common vetch
(Vicia sativa L.) plants. Environ Geochem Health 2003,
25:123-130.
32. White PM Jr, Wolf DC, Thoma GJ, Reynolds CM: Influence of
organic and inorganic soil amendments on plant growth
in crude oil-contaminated soil. Int J Phytoremed 2003,
5:381-398.
33. Karthikeyan R, Mankin KR, Davis LC, Erickson LE: Fate and
transport of jet fuel (JP-8) in soils with selected plants.
Int J Phytoremed 2003a, 5:281-292.
34. Karthikeyan R, Mankin KR, Davis LC, Erickson LE: Modeling jet
fuel (JP-8) fate and transport in soils with plants. Int J
Phytoremed 2003b, 5:293-314.
Phytodegradation of organic compounds Newman and Reynolds 229
www.sciencedirect.com
Current Opinion in Biotechnology 2004, 15:225–230