Skip to main content

Population Diversity and Dynamics of Parasitic Weeds

  • Chapter
  • First Online:
Parasitic Orobanchaceae

Abstract

Knowledge of the genetic diversity of parasitic weed populations is important in any attempt to develop resistance-breeding strategies for the relevant host crops. Moreover, comparative genetic diversity studies of parasite biotypes in natural habitats and crop fields are important for clarifying the evolutionary path from wild parasitic plants to aggressive parasitic weeds. The genetic diversity of plant populations, analysed by isozymes and SSR, RAPD, ISSR and AFLP markers, is determined by dynamics that deal with the variation in time and space of population composition, size and density. The key elements that determine variation in population dynamics and impact the genetic diversity of parasitic weed populations are the population history, the parasite mating system and dispersal strategy, host preferences and issues imposed by agricultural plant communities, including the existence of host resistances, and farming practices.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Aigbokhan E, Berner D, Musselman L, Mignouna H (2000) Evaluation of variability in Striga aspera, Striga hermonthica and their hybrids using morphological characters and random amplified polymorphic DNA markers. Weed Res 40:375–386

    Article  Google Scholar 

  • Benharrat H, Boulet C, Theodet C, Thalouarn P (2005) Virulence diversity among branched broomrape (Orobanche ramosa L.) populations in France. Agron Sustain Dev 25:123–128

    Article  Google Scholar 

  • Berner DK, Cardwell F, Faturori BO, Ikie FO, Williams OA (1994) Relative roles of wind, crop seeds and cattle in dispersal of Striga spp. Plant Dis 78:402–406

    Article  Google Scholar 

  • Bharathalakshmi, Werth CR, Musselman LJ (1990) A study of genetic diversity among host-specific populations of the witchweed Striga hermonthica (Scrophulariaceae) in Africa. Plant Syst Evol 172:1–12

    Google Scholar 

  • Botanga CJ, Timko MP (2005) Genetic structure and analysis of host and non-host interactions of Striga gesnerioides (witchweed) from Central Florida. Phytopathology 95:1166–1173

    Article  PubMed  CAS  Google Scholar 

  • Botanga CJ, Timko MP (2006) Phenetic relationships among different races of Striga gesnerioides (Willd.) Vatke from West Africa. Genome 49:1351–1365

    Article  PubMed  Google Scholar 

  • Botanga CJ, Kling JG, Berner DK, Timko MP (2002) Genetic variability of Striga asiatica (L.) Kuntz based on AFLP analysis and host-parasite interaction. Euphytica 128:375–388

    Article  CAS  Google Scholar 

  • Brault M, Betsou F, Jeune B, Tuquet C, Sallé G (2007) Variability of Orobanche ramosa populations in France as revealed by cross infestations and molecular markers. Environ Exp Bot 61:272–280

    Article  CAS  Google Scholar 

  • Buschmann H, Gonsior G, Sauerborn J (2005) Pathogenicity of branched broomrape (Orobanche ramosa) populations on tobacco cultivars. Plant Pathol 54:650–656

    Article  Google Scholar 

  • Castejón-Muñoz M, Suso MJ, Romero-Muñoz F, García-Torres L (1991a) Isoenzymatic study of Orobanche (Orobanche cernua) populations infesting sunflower (Helianthus annuus). In: Ransom JK, Musselman LJ, Worsham AD, Parker C (eds) International symposium on parasitic weeds. CIMMYT, Nairobi, Kenya, pp 313–319

    Google Scholar 

  • Castejón-Muñoz M, Romero-Muñoz F, García-Torres L (1991b) Orobanche cernua seed dispersal through sunflower achenes. Helia 14:51–54

    Google Scholar 

  • Cubero JI, Moreno MT (1979) Agronomical control and sources of resistance in Vicia faba to Orobanche crenata. In: Bond DA, Scarascia-Mugnozza GT, Poulsen MH (eds) Some current research on Vicia faba in Western Europe. Commission of the European Communities, Luxemburg, pp 41–80

    Google Scholar 

  • Dongo A, Leflon M, Simier P, Delavault P (2012) Development of a high-throughput real-time quantitative PCR method to detect and quantify contaminating seeds of Phelipanche ramosa and Orobanche cumana in crop seed lots. Weed Res 52:34–41

    Article  CAS  Google Scholar 

  • Dubois S, Cheptou PO, Petit C, Meerts P, Poncelet M, Vekemans X, Lefèbvre C, Escarré J (2003) Genetic structure and mating systems of metallicolous and nonmetallicolous populations of Thlaspi caerulescens. New Phytol 157:633–641

    Article  Google Scholar 

  • Eizenberg H, Plakhine D, Landa T, Achdari G, Joel DM, Hershenhorn J (2004) First report of a new race of sunflower broomrape (Orobanche cumana) in Israel. Plant Dis 88:1284

    Article  Google Scholar 

  • Estep MC, Van Mourik T, Muth P, Guindo D, Parzies HK, Koita OA, Weltzien E, Bennetzen JL (2011) Genetic diversity of a parasitic weed, Striga hermonthica, on sorghum and pearl millet in Mali. Trop Plant Biol 4:91–98

    Article  Google Scholar 

  • Frost CC, Musselman LJ (1980) Clover broomrape in the United States. Weed Sci 28:119–122

    Google Scholar 

  • Gagne G, Roeckel-Drevet P, Grezes-Besset B, Shindrova P, Ivanov P, Grand- Ravel C, Vear F, Tourvieille de Labrouhe D, Charmet G, Nicolas P (1998) Study of the variability and evolution of Orobanche cumana populations infesting sunflower in different European countries. Theor Appl Genet 96:1216–1222

    Article  Google Scholar 

  • Gagne G, Roeckel-Drevet P, Grezes-Besset B, Shindrova P, Ivanov P, Grand-Ravel C, Vear F, Charmet G, Nicolas P (2000) Amplified fragment length polymorphism (AFLP) as suitable markers to study Orobanche cumana genetic diversity. J Phytopathol 148:457–459

    Article  CAS  Google Scholar 

  • Gethi G, Smith M, Mitchell S, Kresovich S (2005) Genetic diversity of Striga hermonthica and Striga asiatica populations in Kenya. Weed Res 45:64–73

    Article  CAS  Google Scholar 

  • Ginman E (2009) Dispersal biology of Orobanche ramosa in South Australia. MSc Thesis, The University of Adelaide

    Google Scholar 

  • Hamrick JL, Godt MJW (1989) Allozyme diversity in plant species. In: Brown AHD, Clegg MT, Kahler AL, Weir BS (eds) Plant population genetics, breeding and genetic resources. Sinauer, Sunderland, MA, pp 43–63

    Google Scholar 

  • Hamrick JL, Nason JD (1996) Consequences of dispersal in plants. In: Rhodes EO, Chesser RK, Smith MH (eds) Population dynamics in ecological space and time. University of Chicago Press, Chicago, IL, pp 203–236

    Google Scholar 

  • Ivanov P, Shindrova P, Ivanova I (1998) An isoenzyme analysis of the North-East Bulgarian Orobanche cumana populations. In: Wegmann K, Musselman LJ, Joel DM (eds) Current problems of Orobanche researches. Proceedings of the 4th international workshop on Orobanche. ‘Dubroudja’, Albena, Bulgaria, pp 87–94

    Google Scholar 

  • Joel DM (2000) A new virulent race of Orobanche crenata. Haustorium 37:2

    Google Scholar 

  • Joel DM, Benharrat H, Portnoy H, Thalouarn (1998) Molecular markers for Orobanche species – new approaches and their potential uses. In: Wegmann K, Musselman LJ, Joel DM (eds) Current problems in Orobanche research. Proceedings of the 4th international Orobanche workshop. Albena, Bulgaria, pp 115–124

    Google Scholar 

  • Kharrat M, Halila MH, Linke KH, Haddar T (1992) First report of Orobanche foetida Poiret on faba bean in Tunisia. FABIS Newsl 30:46–47

    Google Scholar 

  • Melero-Vara JM, Domínguez J, Fernández-Martínez JM (2000) Update on sunflower broomrape situation in Spain: racial status and sunflower breeding for resistance. Helia 23:45–56

    Google Scholar 

  • Musselman LJ (1994) Taxonomy and spread of Orobanche. In: Pieterse AH, Verkleij JAC, ter Borg SJ (eds) Biology and management of Orobanche. Proceedings of the third international workshop on Orobanche and related Striga research. Royal Tropical Institute, Amsterdam, The Netherlands, pp 27–35

    Google Scholar 

  • Noubissie Tchiagam JB, Bell JM, Guissai Birwe S, Gonne S, Youmbi E (2010) Varietal response of cowpea (Vigna unguiculata (L.) Walp.) to Striga gesnerioides (Willd.) Vatke Race SG5 Infestation. Notulae Botanicae Horti Agrobotanici Cluj-Napoca 38(2):33–41

    Google Scholar 

  • Pérez-de-Luque A, Fondevilla S, Pérez-Vich B, Aly R, Thoiron S, Simier P, Castillejo MA, Fernández-Martínez JM, Jorrín J, Rubiales D, Delavault P (2009) Understanding Orobanche and Phelipanche-host plant interaction and developing resistance. Weed Res 49:8–22

    Article  Google Scholar 

  • Provine WB (2004) Ernst Mayr: genetics and speciation. Genetics 167:1041–1046

    PubMed  Google Scholar 

  • Radwan MS, Abdalla MMF, Fischbeck G, Metwally AA, Darwish DS (1988) Variation in reaction of faba bean lines to different accessions of Orobanche crenata Forsk. Plant Breed 101:208–216

    Article  Google Scholar 

  • Roberts HA (1981) Seed banks in the soil, vol 6, Advances in applied biology. Academic, Cambridge, 55 p

    Google Scholar 

  • Román B, Rubiales D, Torres AM, Cubero JI, Satovic Z (2001) Genetic diversity in Orobanche crenata populations from southern Spain. Theor Appl Genet 103:1108–1114

    Article  Google Scholar 

  • Román B, Satovic Z, Rubiales D, Torres AM, Cubero JI, Katzir N, Joel DM (2002) Variation among and within populations of the parasitic weed Orobanche crenata from Spain and Israel revealed by inter simple sequence repeat markers. Phytopathology 92:1262–1266

    Article  PubMed  Google Scholar 

  • Román B, Satovic Z, Alfaro C, Moreno MT, Kharrat M, Perez de Luque A, Rubiales D (2007a) Host differentiation in Orobanche foetida Poir. Flora 202:201–208

    Article  Google Scholar 

  • Román B, Hernandez R, Pujadas A, Cubero JI, Rubiales D, Satovic Z (2007b) Genetic diversity in two variants of Orobanche gracilis Sm. [var. gracilis and var. deludens (Beck) A. Pujadas] from different regions of Spain. Electron J Biotechnol 10:221–229

    Article  Google Scholar 

  • Rubiales D, Sadiki M, Román B (2005) First report of Orobanche foetida on common vetch (Vicia sativa) in Morocco. Plant Dis 89:528

    Article  Google Scholar 

  • Satovic Z, Joel DM, Rubiales D, Cubero JI, Román B (2009) Population genetics in weedy species of Orobanche. Australas Plant Pathol 38:228–234

    Article  Google Scholar 

  • Sweigart AL, Willis JH (2003) Patterns of nucleotide diversity in two species of Mimulus are affected by mating system and asymmetric introgression. Evolution 11:2490–2506

    Google Scholar 

  • Thorogood CJ, Rumsey FJ, Harris SA, Hiscock SJ (2008) Host-driven divergence in the parasitic plant Orobanche minor Sm. (Orobanchaceae). Mol Ecol 17:4289–4303

    Article  PubMed  CAS  Google Scholar 

  • Thorogood CJ, Rumsey FJ, Harris SA, Hiscock SJ (2009) Gene flow between alien and native races of the holoparasitic angiosperm Orobanche minor (Orobanchaceae). Plant Syst Evol 282:31–42

    Article  Google Scholar 

  • Vaz Patto MC, Díaz-Ruiz R, Satovic Z, Román B, Pujadas-Salvà AJ, Rubiales D (2008) Genetic diversity of Moroccan populations of Orobanche foetida: from wild parasitic plants to parasitic weeds. Weed Res 48:179–186

    Article  Google Scholar 

  • Vaz Patto MC, Fernández-Aparicio M, Satovic Z, Rubiales D (2009) Extent and pattern of genetic differentiation within and between European populations of Phelipanche ramosa revealed by amplified fragment length polymorphism analysis. Weed Res 49:48–55

    Article  CAS  Google Scholar 

  • Verkleij JAC, Janssen J, Pieterse AH (1986) A preliminary study on isoenzyme variation in Orobanche crenata and Orobanche aegyptiaca from Syria. In: Borg SJ (ed) Proceedings of a workshop on the biology and control of Orobanche, Wageningen, The Netherlands, pp 154–159

    Google Scholar 

  • Verkleij JAC, Koevoets P, López-Granados F, Egbers WS, García-Torres L, Pieterse AH (1991) Genetic variability in populations of Orobanche crenata from Spain. In: Ransom JK, Musselman LJ, Worsham AD, Parker C (eds) International symposium on parasitic weeds. CIMMYT, Nairobi, Kenya, pp 462–469

    Google Scholar 

  • Vrânceanu AV, Tudor VA, Stoenescu FM, Pirvu N (1980) Virulence groups of Orobanche cumana Wallr. differential hosts and resistance sources and genes in sunflower. In: Proceedings of the 9th international sunflower conference, 8–13 July 1980, Torremolinos, Spain, pp 74–80

    Google Scholar 

  • Vrânceanu, AV, Pîrvu N, Stoenescu FM, Pacureanu M (1986) Some aspects of the interaction Helianthus annuus L./Orobanche cumana Wallr. and its implications in sunflower breeding. In: ter Borg S (ed) Proceedings of a workshop on biology and control of Orobanche LH/VPO, Wageningen, The Netherlands, pp 181–189

    Google Scholar 

  • Werth CR, Riopel JL, Gillespie NW (1984) Genetic uniformity in an introduced population of witchweed (Striga asiatica) in the United States). Weed Sci 32:645–648

    Google Scholar 

  • Westwood JH, Fagg CM (2004) ISSR characterization of Orobanche minor populations in the US. In: Joel DM (ed) Proceedings of the eighth international parasitic weeds symposium. IPPS, Durban, South Africa, p 15

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Belén Román .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2013 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Román, B. (2013). Population Diversity and Dynamics of Parasitic Weeds. In: Joel, D., Gressel, J., Musselman, L. (eds) Parasitic Orobanchaceae. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-38146-1_19

Download citation

Publish with us

Policies and ethics