The Role of Plants in Bioremediation of Coal Bed Methane Product Water
Abstract
Coal bed methane (CBM exploration and development has increased substantially over
the past ten years, with the Powder River Basin in Wyoming and Montana emerging as
one of the most active new locations for exploration. Today, almost 6% of total United
States production of methane occurs in this area. Methane extraction co-produces an
excess of water, which can be saline-sodic. The water that is co-produced is spread
onto the land or impounded in ephemeral draws. This water has the potential to elevate
the saline-sodic conditions of the soil, causing decreases in land productivity. It
is hypothesized that specific species of plants can function to uptake excess salts
and remediate the saline-sodic conditions associated with CBM discharge water. Early
research has pointed towards possible successes in this approach. Studies in Europe,
Egypt, and the United States suggest that species called halophytes, defined as "salt
tolerant accumulators", have successfully achieved excess salt uptake by their roots.
These species can accumulate high concentrations of sodium and other salts in their
above ground tissue and, in some cases, can excrete these salts through nodes or on
leaf surfaces. Synthesis of this research suggests that phytoremediation, or remediation
by plants, functions best in rotation or in combination with similar functioning plant
species. Field crops, particularly barley, wheat, sorghum, cotton, and sugar beets,
have been used extensively in phytoremediation of saline-sodic sites worldwide.
CBM Background
Exploration, development, and production within the CBM industry have increased dramatically
over the past ten years. Since 1997, the Powder River Basin in Wyoming and Montana
has emerged as one of the most active new areas of CBM production in the U.S., comprising
nearly 6% of U.S. total production (Rice et al., 2001).
Product Water Volume
As a part of CBM extraction , water is also brought to the land surface. Water extraction
reduces hydrostatic pressure within the coal seam, thereby stimulating desorption
of methane from coal particle surfaces. During CBM production, this water is continuously
pumped into containment areas, discharged to nearby stream channels, or spread onto
the land and into ephemeral stream depressions. As with gas production, water production
has increased significantly as CBM development has advanced. The possibility of millions
of gallons of water discharged per day has become a realistic statistic in recent
literature (Rice et al., 2001).
Product Water Sodicity
Chemistry of CBM product water has been the focus of much research lately. Samples
with relatively high concentrations of salinity and sodicity have been recorded from
wells in the Powder River Basin, as well as the adjacent Tongue River Drainage (Rice
et al., 2001). Sodium adsorption ratios (SAR) and electrical conductivity (EC) levels
of some CBM product water have exceeded published standards for all land uses, with
the exception of domestic and livestock uses. According to the USDA and the University
of California Extension Service, most discharge water is sodic (USDA, 1979). In sodic
soil systems, exchangeable sodium ions are so concentrated in the soil that they may
adversely affect plant growth and often have an adverse effect on soil physical properties.
An SAR of 10 or greater indicates a sodic soil (USDA, 1979).
Sodicity frequently affects soil physical characteristics. The chemical characteristics and hydration status of sodium provide it with properties of a dispersing agent. Excessive sodium, when not balanced with divalent cations, causes soil aggregate structure to disintegrate or disperse. An excess of sodium on the cation exchange sites of fine-textured soils forms a condition in which irrigation water entering the soil is attracted to small pores with a great amount of force, resulting in soil swelling, particle slaking from aggregates, and dispersion, thus precluding drainage. Upon drying, dispersed soil particles undergo a reorientation, resulting in lost soil structure, lower hydraulic conductivity, and surface crusting that can break plant stems, inhibit germination and emergence, and slow infiltration (Dollhopf, 2000).
Adverse impacts of sodicity on dispersion of fine-earth soils are exacerbated by arid
and semi-arid zone environments where rainfall conditions of significance seldom occur
during the irrigation season. This is the period when CBM discharge is likely to contact
surface soils (Rengasamy and Sumner, 1998).
Product Water Salinity
CBM discharge water is characterized by modest saline levels and may pose an environmental
constraint on plant production in affected soils. A saline soil is one containing
sufficient salts to interfere with growth of most plant species and is defined as
having a saturated extract EC greater than 4 mmhos/cm (ds/m) (USDA, 1979), at which
the growth rate of some plant species may decrease. Salinity has the potential to
have significant impacts on plant communities, plant community sustainability, and
livestock and wild life forage capabilities. In the absence of a well drained soil
matrix or adequate irrigation or precipitation, salt leaching may not occur and over
time the soil may become saline.
According to Maas (1993), the most common effect of salinity is a general stunting of growth. They (plants) may have darker green leaves that, in some cases, are thicker and more succulent. Visual symptoms, such as leaf burn, necrosis, and defoliation occur in some species, particularly woody crops. This loss in plant productivity is not solely a phytotoxic response, but is also related to osmotic stress (Bauder et al., 1992).
Increased salt concentration in irrigation water can directly affect pH of the soil environment. Research by Bohn et al. (1985) asserts that increasing salt concentrations usually decrease pH by displacement of hydrogen and aluminum with cations in solution, allowing the aluminum ion to hydrolyze and further lower pH. The lowering of pH can lead to phytotoxic soil characteristics. By decreasing solubility of trace metals in the soil and immobilizing nutrients, plant species production may be limited.
Saline-sodic conditions potentially created by CBM discharge water will require mitigation
in order to return the soil system to past land use capabilities. The notion of reclaiming
salt affected soils was conceived of long before the science of CBM reclamation was
considered. In 1981 Francois (1981) claimed that an efficient, economically feasible
soil reclamation strategy was necessary to reverse deteriorating soil conditions associated
with long-term irrigation with water of relatively high total dissolved solid (TDS)
concentration and SAR.
The Role of Bioremediation
Numerous suggestions have been advanced to remediate the effects of salts in the soil.
At the core of these saline-sodic remediation methods are: 1) amending affected soils
with gypsum treatments, a reclamation technique that has been adopted by soil scientists
throughout the world, 2) leaching, a method to dilute and transport salts by water
inundation, and 3) plant community bioremediation, a function of plant species ability
to mitigate salts in soil solution either by plant uptake or chemical alteration of
the soil. Present research points to the third remediation method as the most environmentally
sustainable method in dealing with the saline-sodic condition. Hoffman (1986), an
agricultural scientist, hypothesized that beneficial effects of plants in reclamation
are not well understood but appear to be related to the physical action of the plant
roots, the addition of organic matter, the increase in dissolution of CaCO3, and crop uptake of salts.
In a publication entitled "Bioreclamation of saline-sodic soil by Amshot grass in Northern Egypt," Helalia et al. (1992) reported the effects of Amshot grass (Echinochloa stagnina) compared to ponding and gypsum on reducing alkalinity and salinity of highly saline-sodic soil in Northern Egypt. Their results indicated that Amshot grass reduced the exchangeable sodium percent (ESP) of the surface layer more than did either ponding or gypsum treatment. Reduction in exchangeable sodium was accompanied by a 42-45% decrease in SAR within the upper 45 cm (18 inches) of soil. In addition, Amshot grass significantly reduced soil salinity compared to either ponding or gypsum and produced higher fresh yield than clover (Melilotus officinalis) cultivated in such soils. Additional studies have led to similar findings. Thus, the role of plants in saline-sodic remediation has become accepted by many of the environmental sciences, and federal funding is increasing in these areas of research and development.
University of California-Riverside professor J. D. Oster (2001) identified four criteria needed to achieve sustainable soil quality and plant production: 1) salt tolerant plant species, 2) cropping strategies that maintain a year round cover to minimize the adverse impacts of rainfall, 3) periodic application of nonsaline-nonsodic irrigation waters, and 4) routine monitoring of soil solution chemistry and irrigation water quality. With this in mind, it can further be hypothesize that selected plant community types, functioning as salt tolerant halophytes, ion accumulators/excretors, and species that tend to promote soil permeability, combined with accurate water management strategies, can reduce some of the negative effects of elevated CBM product water salinity and sodicity.
The term phytoremediation applies to the above hypothesis. Phytoremediation, often
referred to as bioremediation, botanical-bioremediation, or green remediation, is
the use of plants to make contaminants non-toxic. Phytoremediation includes rhizofiltration
(absorption, concentration, and precipitation of heavy metals by plant roots), phytoextraction
(extraction and accumulation of contaminants in harvestable plant tissue such as roots
and shoots), and phytostabilization (absorption and precipitation of contaminants
by plants) (Miller, 1996).
Halophytes
The term halophyte, referring to salt tolerant plants (in Helalia et al., 1990), has
been used in science for many years. Boyko (1966) was one of the first to suggest
that halophytic plants could be used to desalinate soil and water. The hypothesis
set forth by Boyko does not distinguish between sodium and other salts. However, it
stands to reason that plants that are able to accumulate sodium salts could be used
successfully to remove sodium from the substrates they are grown in (Helalia et al.,
1990).
Ion Accumulators
Halophytes have evolved different mechanisms to deal with excess sodium and other
salts in their environments. Some vascular halophytes accumulate high levels of sodium
and other salts in their above grounds tissue while others do not (Gorham et al.,
1987). Two classes of functioning halophytes are ion accumulators and ion extractors.
Both function to phytoremediate excess salinity and sodicity present within the soil
profile. Ion accumulators, also called hyper-accumulators, have evolved to take up
high concentrations of ions as an adaptation mechanism to saline environments. The
accumulations of salts is thought to reduce the requirements for increased wall extensibility,
leaf thickness, and water permeability that might otherwise be required to maintain
positive growth and turgor at low soil water potentials (Rush and Epstein, 1981).
Holmes (2001) has conducted extensive laboratory and field investigations of the ecology of plants in extreme environments in an effort to select plants that are suitable for phytoremediation in saline sites. She has successfully used native halophyter plants to reclaim salt contaminated soils in Ohio, Oklahoma, and Texas. A joint project with Exxon biologists at a site near Houston, TX has met with great success. Holmes (2001) reports that content of sodium in the soil was decreased by 65% two years after planting with salt accumulating plants.
As early as 1964, ion-accumulating species were being used in saline site remediation. Chaudhri et al. (1964) reported on investigations examining the ability of Suaeda vera Forsk (Suaeda fruticosa) to accumulate sodium and other salts. The leaves of this plant were found to contain 9.06% salt on a fresh weight basis. A salt content of 4.29% fresh weight was measured in the stems. On average, a single plant was able to produce 935 g of fresh leaf tissue and 232 g of fresh stem tissue. Based on these values, it was determined that a single plant could accumulate 95 g of salt in its above ground biomass. Considering that a single S. fruticosa plant covers an area of 0.36 square meters, approximately 2,353 kg of salt could be removed from one hectare of soil within a period of one year. The investigator suggested that three times as much salt could be "harvested" if the plants were being more effectively cultivated (Chaudhri et al., 1964; Rengasamay and Sumner, 1998).
Two ion accumulators that have been repeatedly referenced in the scientific literature are rice (Oryza sitiva) and sunflower (Helianthus annuus). Rice cultivation has been recognized to improve saline soils. According to Iwasaki (1987), the salt content of the 5 to 10 cm soil depth was reduced to less than one-fifth the original salt content after a single year of rice cultivation. While improvement of the soil may have been caused primarily by the leaching effect of rice cultivation, the rice plant does contribute to soil improvement by accumulating salts in its shoots (George, 1967).
Bhatt and Indirakutty (1973) reported that 83 kg of sodium could be removed from one hectare of land via accumulation by sunflower plants. The investigators concluded that sunflower plants gradually reduce soil salinity with the harvest of the edible sunflower oil.
EC can also be mitigated by ion accumulating species. Sharp-leaved rush (J. acutus) and Samaar morr rush (J. rigidus), which have traditionally been used for weaving floor mats, are also considered
as an alternative pulp material for paper production. Researchers attempting to reclaim
poorly drained soils in Egypt recognized that these two species are cumulative halophytes
(ion accumulators) which concentrate salts in the upper parts of their shoots. Horizontal
rhizomes of these plants were transferred to a poorly drained, saline soil and allowed
to grow. The amount of total soluble solids (TSS) in the soil was measured before
planting and after harvest. On average, a single growth cycle of J. acutus reduced the TSS of the soil from 1.03% to 0.08% while a decrease from 1.07% to 0.65%
was measured in the soil containing J. rigidus. For J. rigidus, this translated to a decrease in EC from 33 to 20 mmhos/cm (ds/m) in soil having
a 50% saturation percentage (Zahran et al., 1982).
Ion Excretors
Excretive halophytes make up the second component of this functioning class of phytoremediating
plants. Excretive halophytes possess glandular cells or vesiculated trichomes (leaf
hairs), which are able to excrete sodium and other salts from their leaf tissue. Tamarix
species (salt cedar) and Atriplex species (saltbush) are examples of plants that possess
salt excreting glanular cells and trichomes, respectively (Kelly et al, 1982).
Atriplex is from the family Chenopodiaceae, which contains about 20% of all halophyte species (Glenn et al., 2001) and is well known for having very high internal concentrations of sodium ions. Excretive halophytes commonly found in CBM production areas of Montana and Wyoming includes Chenopodium (goosefoot), Kochia (summer cypress), Salicornia (saltwort), Salsola (Russian thistle), and Suaeda (sea blite) (Dorn, 1984). The potential use of Atriplex as a forage or animal feed makes its use for soil salt and sodium removal attractive. A hectare (2.47 acres) of Atriplex has the potential to produce 16,000 kg (35,274 lbs) of dry forage matter per year (Goodin and Mckell, 1970).
Halophytes can further be classified according to the type of mineral ions (salts)
they are able to accumulate or excrete. Chlorine halophytes exhibit an internal ion
composition dominated by Na and Cl ions. This is in contrast to alkali halophytes,
which exibit relatively high concentrations of K+, Mg2+, and Ca2+ (Redman and Fedec, 1987).
Rooting Action
While halophytic species can effectively phytoremediate a saline-sodic system by interacting
with salts in the soil-water environment and reducing them through absorption, the
physical characteristics of rooting can also increase soil permeability and result
in leaching of salts beyond the root zone. Root decomposition frees channels for water
movement, thereby increasing hydraulic conductivity of the soil. Yadav (1975) reported
that the extensive root system of paddy rice loosened the soil, making it more permeable
to leaching of salts.
Other studies have reported that sorghum (Sorghum spp.) increases soil pore sizes and water infiltration and leads to greater saturated hydraulic conductivity (Skidmore et al., 1986). Robbins (1986) reported that a sorghum-sudan grass (Sorghum- Sudanese spp.) hybrid crop produced high soil atmospheric CO2 concentrations and greater Na leaching efficiencies than several other crops and amendment treatments.
Assessments of this research, especially the work by Robbins, suggest that these plant
functions work to phytoremediate best when used in rotation or combination with like
plant species. As early as 1972, studies suggested that alternating or interseeding
plants, in this case barley (Hordium spp.) or rice, would accelerate reclamation and the bioremediation process (Saraswat et
al., 1972).
Cropping Options
Field crops, particularly barley, wheat (Triticum spp.), sorghum (Sorghum spp.), cotton (Gossypium spp.), and sugarbeet, have been used extensively in bioremediation of saline-sodic sites.
By utilizing more water on these crops than actually needed, salts and sodium can
be leached beyond the roots and the soil can be prepared for more sensitive crops
(Oster, 2001). Yadav (1975) and later Bauder et al. (1992) and Bauder and Brock (1992)
present a similar diagnosis to that given by Oster. They suggest that cropping can
play a significant role in reclamation of saline and alkali soils and managed crop
systems are essential for achieving continued improvement of such soils.
Bauder and Brock (1992) concluded that uncropped conditions, which maintain the soil at a relatively high water content and minimize repeated drying and rewetting of the soil, and crops such as sorghum-sudan grass, which cause rapid drying of the soil and create conditions conducive to leaching salts, may be the best combination of conditions to gain maximum efficiency of amendments applied to reclaim saline or sodic soil. They further suggest that a primary halophyte species or combination of like species can help to set the stage for complete restoration by amendments. In the Powder River Basin, this may be the best appraoch to reclamation after CBM production has ended.
In conclusion, product water quality associated with CBM extraction has the potential to significantly impacts soil chemistry, plant community production, and land class capabilities in discharge areas and affected regions. In general, it is hypothesized that plant species, including halophytes, can function to phytoremediate saline-sodic conditions through the intrinsic characteristics possessed by the specific species or community. In combination with scientific irrigation strategies, interseeding, crop rotation, and post discharge amendments, such as with gypsum, pre-development land capabilities can be achieved in these affected systems.
Common Name | Scientific Name | Function |
Amshot Grass
|
Echinochloa stagnina
|
ion accumulator
|
Suada vera Forsk
|
Suaeda fruiticosa
|
ion accumulator
|
Rice
|
Oryza sitiva
|
ion accumulator
|
Sunflower
|
Helianthus annuus
|
ion accumulator
|
Sharp-leaved rush
|
Juncus acutus
|
ion accumulator
|
Samaar morr
|
Juncus rigidus
|
ion accumulator
|
Salt Cedar
|
Tamarix L.
|
ion excretor
|
Goosefoot
|
Chenopodium spp.
|
ion excretor
|
Summer Cypress
|
Kochia spp.
|
ion excretor
|
Salt Wort
|
Salicornia spp.
|
ion excretor
|
Russian Thistle
|
Salsola spp.
|
ion excretor
|
Seablite
|
Suaeda spp.
|
ion excretor
|
Sorghum-sudan grass
|
Sorghum-sudanese
|
soil pore size enhancer
|
Barley
|
Hordium spp.
|
limited ion accumalator
|
Wheat
|
Triticum spp.
|
limited ion accumulator
|
Cotton
|
Gossypium spp.
|
limited ion accumulator
|
Sugarbeet
|
Heterodera spp.
|
limited ion accumulator
|
References
Bauder, J. W., and T. A. Brock. 1992. Crop species, amendments, and water quality effects on selected soil physical properties. Soil Sci Soc. Amer. J. 56:1292-1298.
Bauder, J. W., and T. A. Brock. 2001. Irrigation water quality, soil amendments, and crop effects on sodium leaching. J. Arid Lands Research and Management. 15:101-113.
Bauder, J. W., J. S. Jacobson, and W. T. Lanier. 1992. Alfalfa emergence and survival response to irrigation water quality and soil series. Soil Sci. Soc. Amer. J. Vol. 56.
Bhatt, J. G. and K. N. Indirakutty. 1973. Salt tolerance and salt uptake by sunflower. Plant and Soil. 39: 457-460.
Bohn, H. L., B. L. McNeal, and G. A. O'Connor. 1985. Soil Chemistry sec. Edition. John Whiley and Sons. New York, N.Y.
Boyko, H. 1966. Basic ecological principles of plant growing by irrigation with highly saline or seawater. In: Salinity and Aridity. Ed. H. Boyko. Dr. W. Junk Publishers. The Hauge.
Chaudhri, I., B. H. Shah, N. I. Haqvi, and I. A. Mallic. 1964. Investigations on the role of Suaeda fructicosa Forsk in the revegetation of saline and alkali soils in west Pakistan. Plant and Soil. 21:1-7.
Dollhopf, D. J., 2000. Plant growth on saline and acidic borrow soils. Bozeman Montana. Reclamation Research Unit. MSU, Bozeman. P.89.
Dorn, R. D. 1984.Vascular Plants of Montana. Mountain West Publishing. Cheyenne, WY.
Francois, L. E., 1981. Alfalfa management under saline conditions with zero leaching. Agron J. 73:1042-1046.
George, L. Y. 1967. Accumulation of sodium and calcium by seedling of some cereal crops under saline conditions. Agron J. 59: 297.
Glenn, E. P., J. Jed Brown and James O'Leary. 2001. Irrigation crops with seawater. Sci Amer. April 2001. pgs.112-114
Goodin, J. R. and C. M. Mckell, 1970. Wild land Shrubs-Their Biology and Utilization. International Shrubs Symposium. Atriplex spp. As a potential forage crop in marginal agricultural areas. Queensland Press. Brisbane. 11:158. Reprinted by Utah State Univ. p.494.
Gorham, J., C. Hardy, R. G. Wyn Jones, L. R. Joppa and C. N. Law. 1987. Chromosomal location of the K/Na discriminating character in the D genome of wheat. Theor. Appl.Genet. 74: 584-588.
Helalia, A. M., S. El-Amir, S. T. Abou-Zeid and K. F. Zagholoul. 1990. Bioremediation of saline-sodic soil by amshot grass in northern Egypt. Soil and Tillage Research. 22:109-116.
Hoffman, G. 1986. Guidelines for reclamation of salt-affected soils. Appl. Ag. Research. 1(2): 65-72.
Holmes, P. M., 2001. Mycorrhizal colonization of halophytes in central European salt marshes. Referenced by E. P. Glenn in Scientific Amer. April 2001. pgs. 112-114.
Iwasaki, K. 1987. The effectiveness of salt-accumulating plants in reclaiming salinized soils. Japan. J. Trop. Agr. 31:255.
Kelly, D. B., J. R. Goodin and D. R. Miller. 1982. Biology of Atriplex. In: Tasks For Vegetation Science, Vol. 2 Contributions to the Ecology of Halophytes. Eds. D. N. Sen and K. S. Rajpurohit. Dr. W. Junk Publishers. The Hauge.
Maas, E. V., J. A. Poss, and G. J. Hoffman. 1993. Salinity sensitivity of sorgam at three growth stages. Irrig. Sci. 7:1-11.
Miller, R. 1996. Ground water remediation technologies. TO-96-03. Groundwater Remediation Tech. Analysis Center. Ref. Available at http://www.gwrtac.org/html/tech-over.html#PYTOREM. (verified 3/31/01).
Oster, J. D. 2001. Sustainable use of saline-sodic irrigation waters. 2001 California Plant and Soil Conference. Feb. 2001. Dept. of Environmental Sciences. UOC, Riverside, CA.
Redman, R. E. and P. Fedec. 1987. Mineral composition of halophytes and associated soils in western canada. In: Field Survey of Kocia scoparia Inland Halophytes of the United States. Commun. Soil Sci. Plant Anal. 18:559.
Rengasamy, P. and M. E. Sumner. 1998. Processes involved in sodic behavior. In: ‘Sodic Soils: distribution, properties, management, and environmental consequences.' Eds. M. E. Sumner and R. Naidu. Pp. 35-50. ( Oxford Univ. Press: New York).
Rice, C. A., M. S. Ellis, and J. H. Bullock, Jr. 2001. Water co-produced with coal bed methane in the powder river basin, Wyoming: prelim. compositional data. Open file report 00-372, avalible at http://www.greenwood.cr.usga.gov./energy/Cbmethane/oF00-372/table2.html.
Robbins, C. W. 1986. Carbon dioxide partial pressure in lysimeter soils. Agron. J.. 78:151-158.
Rush, D. W. and E. Epstein. 1981. Breeding and selecting for crop tolerance by the incorporation of wild germplast into a domesticated tomato. J. Amer. Soc. Hort. Sci. 106:669-670.
Saraswat, S. N., P. S. Marwaha, and P. Lal. 1972. Use of crop and other organic materials in the reclamation of saline and alkali soils. Agric. Agro-Ind. 5:8-13.
Skidmore, E. L., J. B. Layton, D. V. Armbrust, and M. L. Hooker. 1986. Soil properties as influenced by cropping and residue management. Soil Sci. Soc. Am. J. 50:415-419.
USDA. 1979. Saline and alkali soils. USDA Agricultural Handbook. Available at http://www.fao.org/docrep.html.
Yadav, J. S. P. 1975. Improvement of saline alkali soils through biological methods. Indian For. (July) Pp. 385-395.
Zahran, M. A. and A.A. Abdel Wahid. 1982. Halophytes and human welfare. In: Tasks for Vegetation Science, Vol. 2. Contributions to the Ecology of Halophytes. Eds. D. N. Sen and K. S. Rajpurohit. Dr. W. Junk Publishers. The Hague.