Skip to main content
Log in

Soil amendment effects on the exotic annual grass Bromus tectorum L. and facilitation of its growth by the native perennial grass Hilaria jamesii (Torr.) Benth

  • Published:
Plant Ecology Aims and scope Submit manuscript

Abstract

Greenhouse experiments were undertaken to identify soil factors that curtail growth of the exotic annual grass Bromus tectorum L. (cheatgrass) without significantly inhibiting growth of native perennial grasses (here represented by Hilaria jamesii [Torr.] Benth). We grew B. tectorum and H. jamesii alone (monoculture pots) and together (combination pots) in soil treatments that manipulated levels of soil phosphorus, potassium, and sodium. Hilaria jamesii showed no decline when its aboveground biomass in any of the applied treatments was compared to the control in either the monoculture or combination pots. Monoculture pots of B. tectorum showed a decline in aboveground biomass with the addition of Na2HPO4 and K2HPO4. Interestingly, in pots where H. jamesii was present, the negative effect of these treatments was ameliorated. Whereas the presence of B. tectorum generally decreased the aboveground biomass of H. jamesii (comparing aboveground biomass in monoculture versus combination pots), the presence of H. jamesii resulted in an enhancement of B. tectorum aboveground biomass by up to 900%. We hypothesize that B. tectorum was able to obtain resources from H. jamesii, an action that benefited B. tectorum while generally harming H. jamesii. Possible ways resources may be gained by B. tectorum from native perennial grasses include (1) B. tectorum is protected from salt stress by native plants or associated soil biota; (2) when B. tectorum is grown with H. jamesii, the native soil biota is altered in a way that favors B. tectorum growth, including B. tectorum tapping into the mycorrhizal network of native plants and obtaining resources from them; (3) B. tectorum can take advantage of root exudates from native plants, including water and nutrients released by natives via hydraulic redistribution; and (4) B. tectorum is able to utilize some combination of the above mechanisms. In summary, land managers may find adding soil treatments can temporarily suppress B. tectorum and enhance the establishment of native plants. However, the extirpation of B. tectorum is unlikely, as many native grasses are likely to facilitate its growth.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Aguiar MR, Sala OE (1994) Competition, facilitation, seed distribution and the origin of patches in a Patagonian steppe. Oikos 70:26–34. doi:10.2307/3545695

    Article  Google Scholar 

  • Allen EB (1984) VA mycorrhizae and colonizing annuals: implications for growth, competition, and succession. In: Williams SE, Allen MF (eds) VA mycorrhizae and reclamation of arid and semi-arid lands. University of Wyoming, Wyoming Agricultural Experiment Station, Dubois, pp 42–52

    Google Scholar 

  • Allen EB, Padgett PE, Bytnerowicz A, Minnich RA (1996) Nitrogen deposition effects on coastal sage vegetation of southern California. In: Bytnerowicz A, Arbaugh MJ, Schilling S (eds) Proceedings of the international symposium on air pollution and climate change effects on forest ecosystems, Riverside, February 1996. USDA Forest Service, PSW-GTR-164, Albany, pp 131–140

  • Allison LE, Moodie CD (1965) Carbonate. In: Black CA (ed) Chemical and microbiological properties. Methods of soil analysis, part 2. American Society of Agronomy, Soil Science Society of America, Madison, pp 1379–1396

    Google Scholar 

  • Awad F, Römheld V, Marschner H (1994) Effect of root exudates on mobilization in the rhizosphere and uptake of iron by wheat plants. Plant Soil 165:213–218. doi:10.1007/BF00008064

    Article  CAS  Google Scholar 

  • Belnap J, Phillips SL (2001) Soil biota in an ungrazed grassland: response to annual grass (Bromus tectorum) invasion. Ecol Appl 11:1261–1275. doi:10.1890/1051-0761(2001)011[1261:SBIAUG]2.0.CO;2

    Article  Google Scholar 

  • Belnap J, Phillips SL, Sherrod S, Moldenke A (2005) Soil biota can change after exotic plant invasion: does this affect ecosystem processes? Ecology 86:3007–3017. doi:10.1890/05-0333

    Article  Google Scholar 

  • Belnap J, Phillips SL, Troxler T (2006) Soil lichen and moss cover and species richness can be highly dynamic: the effects of invasion by the annual exotic grass Bromus tectorum and the effects of climate on biological soil crusts. Appl Soil Ecol 32:63–76. doi:10.1016/j.apsoil.2004.12.010

    Article  Google Scholar 

  • Bever JD (1994) Feedback between plants and their soil communities in an old field community. Ecology 75:1965–1977. doi:10.2307/1941601

    Article  Google Scholar 

  • Biondini M, Klein DA, Redente EF (1988) Carbon and nitrogen losses through root exudation by Agropyron spicatum, A smithii and Bouteloua gracilis. Soil Biol Biochem 20:477–482. doi:10.1016/0038-0717(88)90061-2

    Article  Google Scholar 

  • Bookman PA, Mack RN (1982) Root interaction between Bromus tectorum and Poa pratensis: a three-dimensional analysis. Ecology 63:640–646. doi:10.2307/1936783

    Article  Google Scholar 

  • Booth MS, Caldwell MM, Stark JM (2003) Overlapping resource use in three Great Basin species: implications for community invasibility and vegetation dynamics. J Ecol 91:36–48. doi:10.1046/j.1365-2745.2003.00739.x

    Article  Google Scholar 

  • Bremner JM (1996) Nitrogen-total. In: Sparks DL (ed) Chemical methods. Methods of soil analysis, part 3. American Society of Agronomy, Soil Science Society of America, Madison, pp 1085–1121

    Google Scholar 

  • Bremner JM, Keeney DR (1965) Steam distillation methods for determination of ammonium, nitrate and nitrite. Anal Chim Acta 32:485–495

    Google Scholar 

  • Cakmak I, Oztürk L, Marschner H, Karanlik S, Ekiz H (1996) Zinc-efficient wild grasses enhance release of phytosiderophores under zinc deficiency. J Plant Nutr 19:551–563

    Article  CAS  Google Scholar 

  • Caldwell MM (1990) Water parasitism stemming from hydraulic lift: a quantitative test in the field. Isr J Bot 39:395–402

    Google Scholar 

  • Caldwell MM, Dawson TE, Richards JH (1998) Hydraulic lift: consequences of water efflux from the roots of plants. Oecologia 113:151–161. doi:10.1007/s004420050363

    Article  Google Scholar 

  • Callaway RM, Pugnaire FI (2007) Facilitation in plant communities. In: Pugnaire FI, Valladares F (eds) Functional plant ecology. CRC Press, Boca Raton, pp 435–455

    Google Scholar 

  • Callaway RM, Newingham B, Zabinski C, Mahall BE (2001) Compensatory growth and competitive ability of an invasive weed are enhanced by soil fungi and native neighbors. Ecol Lett 4:429–433. doi:10.1046/j.1461-0248.2001.00251.x

    Article  Google Scholar 

  • Callaway RM, Mahall BE, Wicks C, Pankey J, Zabinski C (2003) Soil fungi and the effects of an invasive forb on grasses: neighbor identity matters. Ecology 84:129–135. doi:10.1890/0012-9658(2003)084[0129:SFATEO]2.0.CO;2

    Article  Google Scholar 

  • Callaway RM, Thelen GC, Barth S, Ramsey PW, Gannon JE (2004) Soil fungi alter interactions between the invader Centaurea maculosa and North American natives. Ecology 85:1062–1071. doi:10.1890/02-0775

    Article  Google Scholar 

  • Cannon JP, Allen EB, Allen MF, Dudley LM, Jurinak JJ (1995) The effects of oxalates produced by Salsola tragus on the phosphorus nutrition of Stipa pulchra. Oecologia 102:265–272. doi:10.1007/BF00329792

    Article  Google Scholar 

  • Carey EV, Marler MJ, Callaway RM (2004) Mycorrhizae transfer carbon from a native grass to an invasive weed: evidence from stable isotopes and physiology. Plant Ecol 172:133–141. doi:10.1023/B:VEGE.0000026031.14086.f1

    Article  Google Scholar 

  • Chapman HD (1965) Cation-exchange capacity. In: Black CA (ed) Chemical and microbiological properties. Methods of soil analysis, part 2. American Society of Agronomy, Soil Science Society of America, Madison, pp 891–901

    Google Scholar 

  • Crooke WM, Knight AH (1962) An evaluation of published data on the mineral composition of plants in the light of the cation-exchange capacities of their roots. Soil Sci 93:365–373. doi:10.1097/00010694-196206000-00001

    Article  CAS  Google Scholar 

  • Dawson TE (1993) Hydraulic lift and water use by plants: implications for water balance, performance and plant-plant interactions. Oecologia 95:565–574

    Google Scholar 

  • Deubel A, Gransee A, Merbach W (2000) Transformation of organic rhizodepositions by rhizosphere bacteria and its influence on the availability of tertiary calcium phosphate. J Plant Nutr Soil Sci 163:387–392. doi :10.1002/1522-2624(200008)163:4<387::AID-JPLN387>3.0.CO;2-K

    Article  CAS  Google Scholar 

  • Drake M, Vengris J, Colby WG (1951) Cation-exchange capacity of plant roots. Soil Sci 72:139–147. doi:10.1097/00010694-195108000-00006

    Article  CAS  Google Scholar 

  • Eckert RE Jr, Evans RA (1963) Responses of downy brome and crested wheatgrass to nitrogen and phosphorus in nutrient solution. Weeds 11:170–174. doi:10.2307/4040573

    Article  Google Scholar 

  • Evans RA (1961) Effects of different densities of downy brome (Bromus tectorum) on growth and survival of crested wheatgrass (Agropyron desertorum) in the greenhouse. Weeds 9:216–223. doi:10.2307/4040408

    Article  Google Scholar 

  • Fischer-Walter LE, Hartnett DC, Hetrick BAD, Schwab AP (1996) Interspecific nutrient transfer in a tallgrass prairie plant community. Am J Bot 83:180–184. doi:10.2307/2445936

    Article  Google Scholar 

  • Freeman DC, Emlen JM (1995) Assessment of interspecific interactions in plant communities: an illustration from the cold desert saltbush grasslands of North America. J Arid Environ 31:179–198. doi:10.1006/jare.1995.0059

    Article  Google Scholar 

  • Greenlee JT, Callaway RM (1996) Abiotic stress and the relative importance of interference and facilitation in montane bunchgrass communities in western Montana. Am Nat 148:386–396. doi:10.1086/285931

    Article  Google Scholar 

  • Gries D, Runge M (1995) Responses of calcicole and calcifuge Poaceae species to iron-limiting conditions. Bot Acta 108:482–489

    CAS  Google Scholar 

  • Grime JP, Mackey JML, Hillier SH, Read DJ (1987) Floristic diversity in a model system using experimental microcosms. Nature 328:420–422. doi:10.1038/328420a0

    Article  Google Scholar 

  • Harper KT, Van Buren R, Kitchen SG (1996) Invasion of alien annuals and ecological consequences in salt desert shrublands of western Utah. In: Barrow JR, McArthur ED, Sosebee RE, Tausch RJ (eds) Proceedings: shrubland ecosystem dynamics in a changing environment, Las Cruces, May 1995. USDA Forest Service, INT-GTR-338, Ogden, pp 58–65

  • Hawkes CV, Belnap J, D’Antonio CM, Firestone MK (2006) Arbuscular mycorrhizal assemblages in native plant roots change in the presence of invasive exotic grasses. Plant Soil 281:367–379. doi:10.1007/s11104-005-4826-3

    Article  CAS  Google Scholar 

  • Herron GJ, Sheley RL, Maxwell BD, Jacobsen JS (2001) Influence of nutrient availability on the interaction between spotted knapweed and bluebunch wheatgrass. Restor Ecol 9:326–331. doi:10.1046/j.1526-100x.2001.009003326.x

    Article  Google Scholar 

  • Holzapfel C, Mahall BE (1999) Bidirectional facilitation and interference between shrubs and annuals in the Mojave Desert. Ecology 80:1747–1761

    Google Scholar 

  • Howell W (1998) Germination and establishment of Bromus tectorum L. in relation to cation exchange capacity, seedbed, litter, soil cover and water. Master’s thesis, Prescott College

  • Humphrey LD, Schupp EW (2004) Competition as a barrier to establishment of a native perennial grass (Elymus elymoides) in alien annual grass (Bromus tectorum) communities. J Arid Environ 58:405–422. doi:10.1016/j.jaridenv.2003.11.008

    Article  Google Scholar 

  • Kelrick MI (1991) Factors affecting seeds in a sagebrush-steppe ecosystem and implications for the dispersion of an annual plant species, cheatgrass (Bromus tectorum L.). Ph.D. Dissertation, Utah State University

  • Kleiner EF, Harper KT (1972) Environment and community organization in grasslands of Canyonlands National Park. Ecology 53:299–309. doi:10.2307/1934086

    Article  Google Scholar 

  • Kleiner EF, Harper KT (1977) Occurrence of four major perennial grasses in relation to edaphic factors in a pristine community. J Range Manage 30:286–289. doi:10.2307/3897307

    Article  Google Scholar 

  • Klironomos JN (2002) Feedback with soil biota contributes to plant rarity and invasiveness in communities. Nature 417:67–70. doi:10.1038/417067a

    Article  PubMed  CAS  Google Scholar 

  • Kolb A, Alpert P (2003) Effects of nitrogen and salinity on growth and competition between a native grass and an invasive congener. Biol Invasions 5:229–238. doi:10.1023/A:1026185503777

    Article  Google Scholar 

  • Kotanen PM, Bergelson J, Hazlett DL (1998) Habitats of native and exotic plants in Colorado shortgrass steppe: a comparative approach. Can J Bot 76:664–672. doi:10.1139/cjb-76-4-664

    Article  Google Scholar 

  • Lajtha K, Harrison AF (1995) Strategies of phosphorus acquisition and conservation by plant species and communities. In: Tiessen H (ed) Phosphorus in the global environment: transfers, cycles, and management. SCOPE 54. Wiley, Chichester, pp 140–147

    Google Scholar 

  • Lindsay WL, Norvell WA (1978) Development of a DTPA soil test for zinc, iron, manganese, and copper. Soil Sci Soc Am J 42:421–428

    CAS  Google Scholar 

  • Lowe PN, Lauenroth WK (2003) Effects of nitrogen availability on competition between Bromus tectorum and Bouteloua gracilis. Plant Ecol 167:247–254. doi:10.1023/A:1023934515420

    Article  Google Scholar 

  • Mack RN (1981) Invasion of Bromus tectorum L. into western North America: an ecological chronicle. Agro-Ecosystems 7:145–165. doi:10.1016/0304-3746(81)90027-5

    Article  Google Scholar 

  • Marschner H (1995) Ion uptake mechanisms of individual cells and roots: short-distance transport. Mineral nutrition of higher plants. Academic Press, San Diego, pp 6–78

    Google Scholar 

  • Miller ME (2000) Effects of resource manipulations and soil characteristics on Bromus tectorum L. and Stipa hymenoides R. & S. in calcareous soils of Canyonlands National Park, Utah. Ph.D. Dissertation, University of Colorado

  • Miller ME, Belnap J, Beatty S, Reynolds RL (2006) Performance of Bromus tectorum L. in relation to soil properties, water additions, and chemical amendments in calcareous soils of southeastern Utah, USA. Plant Soil 288:1–18. doi:10.1007/s11104-006-0058-4

    Article  CAS  Google Scholar 

  • Ming DW, Mumpton FA (1989) Zeolites in soils. In: Dixon JB, Weed SB (eds) Minerals in soil environments. Soil Science Society of America, Madison, pp 873–911

    Google Scholar 

  • Monsen SB (1994) The competitive influences of cheatgrass (Bromus tectorum) on site restoration. In: Monsen SB, Kitchen SG (eds) Symposium on ecology, management and restoration of intermountain annual rangelands, Boise, 18–22 May 1992. USDA Forest Service, INT-GTR-313, Ogden, pp 43–50

  • Morrison R (1999) Potassium as a limiting nutrient for germination and production of cheatgrass (Bromus tectorum) in the Canyonlands National Park, Utah. Dissertation, University of Denver

  • Moyer-Henry KA, Burton JW, Israel DW, Rufty TW (2006) Nitrogen transfer between plants: a 15N natural abundance study with crop and weed species. Plant Soil 282:7–20

    Article  CAS  Google Scholar 

  • Newingham B, Belnap J (2006) Direct effects of soil amendments on field emergence and growth of the invasive annual grass Bromus tectorum L. and the native perennial grass Hilaria jamesii (Torr.) Benth. Plant Soil 280:29–40. doi:10.1007/s11104-005-8551-8

    Article  CAS  Google Scholar 

  • Olsen SR, Cole CV, Watanabe FS, Dean LA (1954) Estimation of available phosphorus in soils by extraction with sodium bicarbonate. US Department of Agriculture, Circular No. 939, Washington DC, pp 1–9

  • Peek MS, Leffler AJ, Ivans CY, Ryel RJ, Caldwell MM (2005) Fine root distribution and persistence under field conditions of three co-occurring Great Basin species of different life form. New Phytol 165:171–180. doi:10.1111/j.1469-8137.2004.01186.x

    Article  PubMed  Google Scholar 

  • Rasmuson KE, Anderson JE (2002) Salinity affects development, growth, and photosynthesis in cheatgrass. J Range Manage 55:80–87. doi:10.2307/4003267

    Article  Google Scholar 

  • Rhoades JD (1982) Soluble salts. In: Page AL (ed) Chemical and microbiological properties. Methods of soil analysis, part 2. American Society of Agronomy, Soil Science Society of America, Madison, pp 167–179

    Google Scholar 

  • Sannazzaro AI, Ruiz OA, Albertó EO, Menéndez AB (2006) Alleviation of salt stress in Lotus glaber by Glomus intraradices. Plant Soil 285:279–287. doi:10.1007/s11104-006-9015-5

    Article  CAS  Google Scholar 

  • Schoenau JJ, Karamonos RE (1993) Sodium bicarbonate extractable P, K and N. In: Carter MR (ed) Soil sampling and methods of analysis. Canadian Society of Soil Science, Ottawa, pp 51–58

    Google Scholar 

  • Scott D, Billings WD (1964) Effects of environmental factors on standing crop and productivity of an alpine tundra. Ecol Monogr 34:243–270. doi:10.2307/1948502

    Article  Google Scholar 

  • Shen YY, Li Y, Yan GY (2003) Effects of salinity on germination of six salt-tolerant forage species and their recovery from saline conditions. N Z J Agric Res 46:236–269

    Google Scholar 

  • Sperry LJ, Belnap J, Evans RD (2006) Bromus tectorum invasion alters nitrogen dynamics in an undisturbed arid grassland ecosystem. Ecology 87:603–615. doi:10.1890/05-0836

    Article  PubMed  CAS  Google Scholar 

  • Staunton S, LePrince F (1996) Effect of pH and some organic anions on the solubility of soil phosphate: implications for P availability. Eur J Soil Sci 47:231–239. doi:10.1111/j.1365-2389.1996.tb01394.x

    Article  CAS  Google Scholar 

  • Ström L, Olsson T, Tyler G (1994) Differences between calcifuge and acidifuge plants in root exudation of low-molecular organic acids. Plant Soil 167:239–245. doi:10.1007/BF00007950

    Article  Google Scholar 

  • Tausch RJ, Svejcar T, Burkhardt JW (1994) Patterns of annual grass dominance on Anaho Island: implications for Great Basin vegetation management. In: Monsen SB, Kitchen SG (eds) Symposium on ecology, management and restoration of intermountain annual rangelands, Boise, 18–22 May 1992. USDA Forest Service, INT-GTR-313, Ogden, pp 120–125

  • Thomas GW (1982) Exchangeable cations. In: Page AL (ed) Chemical and microbiological properties. Methods of soil analysis, part 2. American Society of Agronomy, Soil Science Society of America, Madison, pp 159–165

    Google Scholar 

  • Trappe JM (1981) Mycorrhizae and productivity of arid and semiarid rangelands. In: Manassah JT, Briskey EJ (eds) Advances in food-producing systems for arid and semiarid lands. Academic Press, New York, pp 581–599

    Google Scholar 

  • Troeh FR, Thompson LM (1993) Soils and soil fertility. Oxford, New York

    Google Scholar 

  • Tyler G (1992) Inability to solubilize phosphate in limestone soils: key factor controlling calcifuge habit of plants. Plant Soil 145:65–70. doi:10.1007/BF00009542

    Article  CAS  Google Scholar 

  • Tyler G (1994) A new approach to understanding the calcifuge habit of plants. Ann Bot (Lond) 73:327–330. doi:10.1006/anbo.1994.1038

    Article  Google Scholar 

  • Tyler G, Ström L (1995) Differing organic acid exudation pattern explains calcifuge and acidifuge behaviour of plants. Ann Bot (Lond) 75:75–78. doi:10.1016/S0305-7364(05)80011-3

    Article  CAS  Google Scholar 

  • Upadhyaya MK, Turkington R, McIlvride D (1986) The biology of Canadian weeds. 75. Bromus tectorum L. Can J Plant Sci 66:689–709

    Article  Google Scholar 

  • Vail D (1994) Management of semi-arid rangelands – impacts of annual weeds on resource values. In: Monsen SB, Kitchen SG (eds) Symposium on ecology, management and restoration of intermountain annual rangelands, Boise, 18–22 May 1992. USDA Forest Service, INT-GTR-313, Ogden, pp 3–5

  • Walkley A, Black IA (1934) An examination of Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Sci 37:29–37. doi:10.1097/00010694-193401000-00003

    Article  CAS  Google Scholar 

  • Wardle DA, van der Putten WH (2002) Biodiversity, ecosystem functioning and above-ground-below-ground linkages. In: Loreau M, Naeem S, Inchausti P (eds) Biodiversity and ecosystem functioning. Oxford University Press, Oxford, pp 155–168

    Google Scholar 

  • Welsh SL, Atwood ND, Goodrich S, Higgins LC (1993) A Utah flora. Brigham Young University, Provo

    Google Scholar 

  • Whisenant SG (1990) Changing fire frequencies on Idaho’s Snake River plains: ecological and management implications. In: McArthur ED, Romney EM, Smith SD, Tueller PT (eds) Symposium on cheatgrass invasion, shrub die-off, and other aspects of shrub biology and management, Las Vegas, April 1989. USDA Forest Service, GTR-INT-276, Ogden, pp 4–10

  • Woodward RA, Harper KT, Tiedemann AR (1984) An ecological consideration of the significance of cation-exchange capacity of roots of some Utah range plants. Plant Soil 79:169–180. doi:10.1007/BF02182339

    Article  CAS  Google Scholar 

  • Yoder CK, Nowak RS (2000) Phosphorus acquisition by Bromus madritensis ssp. rubens from soil interspaces shared with Mojave Desert shrubs. Funct Ecol 14:685–692. doi:10.1046/j.1365-2435.2000.00482.x

    Article  Google Scholar 

  • Zabinski C, Quinn L, Callaway RM (2002) Phosphorus uptake, not carbon transfer, explains arbuscular mycorrhizal enhancement of Centaurea maculosa in the presence of native grassland species. Funct Ecol 16:758–765. doi:10.1046/j.1365-2435.2002.00676.x

    Article  Google Scholar 

  • Zhang F, Romheld F, Marschner H (1991) Release of Zn mobilizing root exudates in different plant species as affected by Zn nutritional status. J Plant Nutr 14:675–686

    Article  CAS  Google Scholar 

  • Zhang FS, Ma J, Cao YP (1997) Phosphorus deficiency enhances root exudation of low-molecular organic acids and utilization of sparingly soluble inorganic phosphates by radish (Raghanus satiuvs L.) and rape (Brassica napus L.) plants. Plant Soil 196:261–264. doi:10.1023/A:1004214410785

    Article  CAS  Google Scholar 

Download references

Acknowledgments

Many thanks to Mark Miller, Sue Phillips, Tina Kister, and Christy Parry for help with the study and manuscript preparation. Funding was provided by the Department of Defense Strategic Environmental Research and Development Program and the US Geological Survey. The use of trade, product, or firm names in this publication is for descriptive purposes only and does not imply endorsement by the US Government.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jayne Belnap.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Belnap, J., Sherrod, S.K. Soil amendment effects on the exotic annual grass Bromus tectorum L. and facilitation of its growth by the native perennial grass Hilaria jamesii (Torr.) Benth. Plant Ecol 201, 709–721 (2009). https://doi.org/10.1007/s11258-008-9463-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11258-008-9463-5

Keywords

Navigation