Skip to main content Skip to main navigation menu Skip to site footer
  • Register
  • Login
  • Menu
  • Home
  • Current
  • Archives
  • Announcements
  • About
    • About the Journal
    • Submissions
    • Editorial Team
    • Privacy Statement
    • Contact
  • Register
  • Login

Ecological Questions

Allelopathic potential of Lupinus polyphyllus L. in relation to habitat variables
  • Home
  • /
  • Allelopathic potential of Lupinus polyphyllus L. in relation to habitat variables
  1. Home /
  2. Archives /
  3. Vol. 37 No. 2 (2026): Forthcoming /
  4. Articles

Allelopathic potential of Lupinus polyphyllus L. in relation to habitat variables

Authors

  • Milena Powolny https://orcid.org/0009-0005-3612-6531
  • Daniel Pruchniewicz Wrocław University of Environmental and Life Sciences Department of Botany and Plant Ecology pl. Grunwaldzki 24a 50-363 Wrocław, Poland https://orcid.org/0000-0002-9841-0192

DOI:

https://doi.org/10.12775/EQ.2026.020

Keywords

Allelopathy, invasive species, target species, habitat factors, water extracts, volatile compounds

Abstract

Lupinus polyphyllus L. is an invasive species widely spread in Europe. Despite many studies on perennial lupine, relatively few have explored its allelopathic potential. . Hence, the aim of this study was to determine the allelopathic effects of three perennial lupine populations originating from various habitats (lowland – S1, foothill – S2 and mountain – S3) on the growth and development of two target species – white mustard (Sinapis alba L.) and meadow red-fescue (Festuca rubra L.). The goal was to determine which of the habitat factors have the greatest influence on the allelopathic potential of this species. The results of conducted research have not demonstrated the existence of clear dependencies which could allow to determine which populations of perennial lupine have the strongest allelopathic potential to inhibit the seed germination and growth of the target species. Among the analyzed habitat factors in laboratory conditions, low concentrations of phosphorus in the soil can stimulate the production of allelochemicals inhibiting the seed germination of the two target species - S. alba and F. rubra.

 

References

Akritidu, K.P.; Boinik, V.V.; Demeshko, O.V. 2013. Organic acids from Lupinus polyphyllus roots. Chem. Nat. Compd., 49, 501–502. https://doi.org/10.1007/s10600-013-0649-2.

Allen S.E. 1989. Chemical Analysis of Ecological Materials. Second Edition, Blackwell Scientific Publications, pp. 367.

Barazani, O.; Friedman, J. 2001. Allelopathic bacteria and their impact on higher plants, Crit. Rev. Microbiol, 27: 41–55.

Boinik, V.V.; Akritidu, K.P.; Demeshko, O.V. 2015. Phenolic compounds from roots of Lupinus polyphyllus. Chem. Nat. Compd., 51, 352–352. https://doi.org/10.1007/s10600-015-1280-1.

Callaway, R.M.; Aschehoug, E.T. 2000. Invasive plants versus their new and old neighbors: A mechanism for exotic invasion. Science, 290, 521–523. https://doi.org/10.1126/science.290.5491.521

Callaway, R.M.; Ridenour, W.M.; Laboski, T.; Weir, T.; Vivanco, J.M. 2005. Natural selection for resistance to the allelopathic effects of invasive plants. Journal of Ecology, 93, 576–583. https://doi.org/10.1111/j.1365-2745.2005.00994.x

Duke, S.O.; Cedergreen, N.; Velini, E.D.; Belz, R.G. 2006. Hormesis: is it an important factor in herbicide use and allelopathy? Outlooks Pest Manag, 17, 29–33.

Eckstein, R.L.; Welk, E.; Klinger, Y.P.; Lennartsson, T.; Wissman, J.; Ludewig, K.; Hansen, W.; Ramula, S. 2023. Biological flora of Central Europe – Lupinus polyphyllus Lindley. Perspectives in Plant Ecology, Evolution and Systematics, 58, 125715.

Einhellig, F.A. 1996. Interactions involving allelopathy in cropping systems: allelopathy in cropping systems. Agronomy J., 88: 883–893.

Fremstad, E. 2010. NOBANIS – Invasive Alien Species Fact Sheet – Lupinus polyphyllus. Online Database of the European Network on Invasive Alien Species, NOBANIS. www.nobanis.org

Gent, M.P.N.; Parrish, Z.D.; White, J.C. 2005. Nutrient uptake amongst the sub species of Cucurbita pepo L. is related to exudation of citric acid. J Amer Soc Hort Sci., 130, 782–788.

Hejda, M.; Pyšek, P.; Jarošík, V. 2009. Impact of invasive plants on the species richness, diversity and composition of invaded communities. Journal of Ecology, 97, 393–403, doi:10.1111/j.1365-2745.2009.01480.x

Hiltbrunner, E.; Aerts, R.; Buhlmann, T.; Huss-Danell, K.; Magnusson, B.; Myrold, D.D.; Reed, S.C.; Sigurdsson, B.D.; Korner, C. 2014. Ecological consequences of the expansion of N2-fixing plants in cold biomes. Oecologia, 176 (1), 11–24. https://doi.org/10.1007/s00442-014-2991-x

Iannucci, A.; Fragasso, M.; Platani, C.; Papa, R. 2013. Plant growth and phenolic compounds in the rhizosphere soil of wild oat (Avena fatua L.). Frontiers in Plant Science, 4 (509), 1e7. http://dx.doi.org/10.3389/fpls.2013.00509.

Kalske, A.; Blande, J.D.; Ramula, S. 2022a. Soil microbiota explain differences in herbivore resistance between native and invasive populations of a perennial herb. J. Ecol., 110, 2649–2660. https://doi.org/10.1111/1365-2745.13975.

Kalske, A.; Mäkinen, E.; Ramula, S. 2022b. Allelopathy by the invasive garden lupine inhibits the germination of native herbs. Botany, 101 (1), 24–29. https://doi.org/10.1139/cjb-2022–0076.

Koeppe, D.E.; Southwick, L.M.; Bittell, J.E. 1976. The relationship of tissue chlorogenic acid concentration and leaching of phenolics from sunflowers grown under varying phosphate nutrient conditions, Can. J. Bot., 54, 593–599.

Latif, S.; Chiapusio, G.; Weston, L.A. 2017. Allelopathy and the Role of Allelochemicals in Plant Defence. In G. Becard (Ed.), How Plants Communicate with their Biotic Environment, 19–54.

Loydi, A.; Donath, T.W.; Eckstein, R.L.; Otte, A. 2015. Non-native species litter reduces germination and growth of resident orbs and grasses: allelopathic, osmotic or mechanical effects? Biol Invasions, 17, 581–595, DOI 10.1007/s10530-014-0750-x

Ludewig, K.; Klinger, Y.; Donath, T.; Bärmann, L.; Eichberg, C.; Thomsen, J.; Görzen, E.; Hansen, W.; Hasselquist, E.; Helminger, T.; Kaiskog, F.; Karlsson, E.; Kirchner, T.; Knudsen, C.; Lenzewski, N.; Lindmo, S.; Milberg, P.; Pruchniewicz D.; Richter, E.; Sandner, T.; Sarneel, J.; Schmiede, R.; Schneider, S.; Schwarz, K.; Tjäder, Å.; Tokarska‐Guzik, B.; Walczak, C.; Weber, O.; Żołnierz, L.; Eckstein, R. 2022. Phenology and morphology of the invasive legume Lupinus polyphyllus along a latitudinal gradient in Europe. NeoBiota, 78, 185–206. DOI:10.3897/neobiota.78.89673

Lyytinen, A.; Lindstrӧm, L. 2019. Responses of a native plant species from invaded and uninvaded areas to allelopathic effects of an invader. Ecology and Evolution, 9: 6116–6123. DOI: 10.1002/ece3.5195

Mahmood, K.; Khan, M.B.; Song, Y.Y.; Ijaz, M.; Luo, S.M.; Zeng, R.S. 2013. UV irradiation enhances rice allelopathic potential in rhizosphere soil. Plant Growth Regulation, 71(1), 21e29. http://dx.doi.org/10.1007/s10725-013-9804-9.

Mardani, H.; Kazantseva, E.; Onipchenko, V.; Fujii, Y. 2016. Evaluation of allelopathic activity of 178 Caucasian plant species. International Journal of Basic and Applied Sciences, 5 (1), 75–81.

Muzquiz, M.; de la Cuarda, C.; Cuadrado, C.; Burbano, C.;, Calvo, R. 1994. Herbicide-like effect of Lupinus alkaloids. Ind Crop Prod, 2: 273–280. https://doi.org/10.1016/0926-6690(94)90118-X

Oberdorfer, E. Pflanzensoziologische Exkursionsflora: Für Deutschland und angrenzende Gebiete (in German) 2001.

Otte, A.; Maul, P. 2005. Verbreitungsschwerpunkte und strukturelle Einnischung der Stauden- Lupine (Lupinus polyphyllus Lindl.) in Bergwiesen der Rhon. Tuexenia, 25, 151–182.

Polyak, Y.M., Sukcharevich VI 2019. Allelopathic Interactions between Plants and Microorganisms in Soil Ecosystems. Biology Bulletin Reviews, 9 (6): 562–574.

Pribyl, D.W. 2010. A critical review of the conventional SOC to SOM conversion factor. Geoderma 2010, 156: 75-83.

Pruchniewicz, D. 2017. Abandonment of traditionally managed mesic mountain meadows affects plant species composition and diversity. Basic Appl. Ecol., 20, 10–18. https://doi.org/10.1016/j.baae.2017.01.006.

Pruchniewicz, D.; Halarewicz, A. Allelopathic effects of wood small-reed (Calamagrostis epigejos) on germination and growth of selected grassland species. Polish Journal of Ecology 2019, 67 (2): 122–136. DOI:10.3161/15052249PJE2019.67.2.003

Radojevic, M.; Bashkin, V. 2006. Plant analysis. [w:] Practical Environmental Analysis pod red. M. Radojevic i V. Bashkin. Royal Society of Chemistry Publishing Cambridge, pp. 457.

Reigosa, M.J.; Pedrol, N.; Sanchez-Moreiras, A.M.; Gonzalez, L. 2022. Stress and allelopathy, in Allelopathy: From Molecules to Ecosystems, Reigosa, M.J. and Pedrol, N., Eds., Enfield, NH: Science, 231-256.

Rice, E.L. 1984. Allelopathy (2nd ed.). San Diego, CA Academic Press.

Rothmaler, W. Exkursionflora für die Gebiete der DDR und die BRD. Bd. 2. Gefässpflanzen, Bd. 4. Kritischer Band. Volk u. Volkseigener Verl., Berlin.2002.

Sebald, O.; Seybold, S.; Philippi, G. Die Farn- und Blütenpflanzen von Baden-Württemberg. Band 3: Spezieller Teil (Spermatophyta, Unterklasse Rosidae), Droseraceae bis Fabaceae. Eugen Ulmer,, Verlag, Stuttgart. 1992.

Tang, C.H.; Cai, W.F.; Kohl, K.; Nishimote, R.K. 1995. Plant stress and allelopathy, in Allelopathy, Organisms, Processes, and Applications, Inderjit, Dakshini, K.M.M., and Einhellig, F.A., Eds., Washington DC: Am. Chem. Soc., 142–157.

Tibico Software Inc. Statistica, Version 13; Tibico Software Inc.: Palo Alto, CA, USA, 2017, Available online: http://statistica.io

Tyler, T.; Karlsson, T.; Milberg, P.; Sahlin, U.; Sundberg, S. 2015. Invasive plant species in the Swedish flora: developing criteria and definitions, and assessing the invasiveness of individual taxa. Nord. J. Bot. , 33, 300–317. https://doi.org/10.1111/njb.00773.

Valtonen, A.; Jantunen, J.; Saarinen, K. 2006. Flora and lepidoptera fauna adversely affected by invasive Lupinus polyphyllus along road verges. Biol. Cons., 133: 389-396. https://doi.org/10.1016/j.biocon.2006.06.015.

Weston, P.A.; Weston, L.A.; Hildebrand, S. 2013. Metabolic profiling in Echium plantagineum L: presence of bioactive pyrrolizidine alkaloids and napthoquinones from accessions across southeastern Australia. Phytochemistry Reviews, 12 (4), 831e837. http://dx.doi.org/10.1007/s11101-013-9306-4.

Wink, M. 1983 Inhibition of seed germination by quinolizidine alkaloids. Aspects of allelopathy in Lupinus albus L. Planta, 158, 365–368.

Wink, M.; Witte, L.; Hartmann, T.; Theuring, C.; Volz, V. 1983. Accumulation of quinolizidine alkaloids in plants and cell suspension cultures: genera Lupinus, Cytisus, Baptisia, Genista, Laburnum, and Sophora. Planta Med., 48, 253–257. https://doi.org/10.1055/s-2007-969928.

Zhang, Z.; Liu, Y.; Yuan, L.; Weber, E.; van Kleunen, M. 2021. Effect of allelopathy on plant performance: a meta-analysis. Ecology Letters, 24 (2), 348–362. https://doi.org/10.1111/ele.13627

Downloads

  • pdf

Published

2026-04-20

How to Cite

1.
MILENA POWOLNY and DANIEL PRUCHNIEWICZ. Allelopathic potential of Lupinus polyphyllus L. in relation to habitat variables. Ecological Questions. Online. 20 April 2026. Vol. 37, no. 2, pp. 1-18. [Accessed 20 April 2026]. DOI 10.12775/EQ.2026.020.
  • ISO 690
  • ACM
  • ACS
  • APA
  • ABNT
  • Chicago
  • Harvard
  • IEEE
  • MLA
  • Turabian
  • Vancouver
Download Citation
  • Endnote/Zotero/Mendeley (RIS)
  • BibTeX

Issue

Vol. 37 No. 2 (2026): Forthcoming

Section

Articles

License

Copyright (c) 2026 Milena Powolny, Daniel Pruchniewicz

Creative Commons License

This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License.

Stats

Number of views and downloads: 6
Number of citations: 0

Search

Search

Browse

  • Browse Author Index
  • Issue archive

User

User

Current Issue

  • Atom logo
  • RSS2 logo
  • RSS1 logo

Information

  • For Readers
  • For Authors
  • For Librarians

Newsletter

Subscribe Unsubscribe

Tags

Search using one of provided tags:

Allelopathy, invasive species, target species, habitat factors, water extracts, volatile compounds
Up

Akademicka Platforma Czasopism

Najlepsze czasopisma naukowe i akademickie w jednym miejscu

apcz.umk.pl

Partners

  • Akademia Ignatianum w Krakowie
  • Akademickie Towarzystwo Andragogiczne
  • Fundacja Copernicus na rzecz Rozwoju Badań Naukowych
  • Instytut Historii im. Tadeusza Manteuffla Polskiej Akademii Nauk
  • Instytut Kultur Śródziemnomorskich i Orientalnych PAN
  • Instytut Tomistyczny
  • Karmelitański Instytut Duchowości w Krakowie
  • Ministerstwo Kultury i Dziedzictwa Narodowego
  • Państwowa Akademia Nauk Stosowanych w Krośnie
  • Państwowa Akademia Nauk Stosowanych we Włocławku
  • Państwowa Wyższa Szkoła Zawodowa im. Stanisława Pigonia w Krośnie
  • Polska Fundacja Przemysłu Kosmicznego
  • Polskie Towarzystwo Ekonomiczne
  • Polskie Towarzystwo Ludoznawcze
  • Towarzystwo Miłośników Torunia
  • Towarzystwo Naukowe w Toruniu
  • Uniwersytet im. Adama Mickiewicza w Poznaniu
  • Uniwersytet Komisji Edukacji Narodowej w Krakowie
  • Uniwersytet Mikołaja Kopernika
  • Uniwersytet w Białymstoku
  • Uniwersytet Warszawski
  • Wojewódzka Biblioteka Publiczna - Książnica Kopernikańska
  • Wyższe Seminarium Duchowne w Pelplinie / Wydawnictwo Diecezjalne „Bernardinum" w Pelplinie

© 2021- Nicolaus Copernicus University Accessibility statement Shop