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2011 | 53 | 1 |

Tytuł artykułu

Cytoembryological analysis of causes for poor seed set in alfalfa (Medicago sativa L.)

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Języki publikacji

EN

Abstrakty

EN
Poor seed set is a limiting factor in alfalfa breeding, as it slows the selection response. One strategy used to overcome this problem is to search for mutations of inflorescence morphology. Long-peduncle (lp), branched-raceme (br) and top-flowering (tf) inflorescence mutations increase the number of flowers per inflorescence, but they do not improve seed set per flower. Here we assessed pollen tube growth in styles of those inflorescence mutants and we observed embryo and endosperm development in seeds 1 to 16 days after pollination (DAP). The number of pollen tubes penetrating the style and the ovary was similar in all tested mutants and in the reference cultivar Radius. At 2 DAP, fertilized ovules were 2.7–3.9 times less numerous in certain inflorescence mutants than in the short-raceme cv. Radius. Ovule degeneration progressed at 2–4 DAP in all analyzed plants. Most ovules were not properly developed in the control cultivar (62%), nor in the forms with mutated inflorescence morphology (69–86%). The number of seeds per pod was lowest in the tf form despite its having the highest number of ovules per ovary. It appears that the number of ovules per pistil is not a crucial factor in seed set in alfalfa when fertilization efficiency is very low. Both poor fertilization and gradual ovule degeneration were factors causing poor seed set in the investigated alfalfa genotypes.

Wydawca

-

Rocznik

Tom

53

Numer

1

Opis fizyczny

p.96-101,fig.,ref.

Twórcy

autor
  • Department of General Botany, Adam Mickiewicz University, Umultowska 89, 61-614 Poznan, Poland
autor
autor

Bibliografia

  • BOLANOS-AGUILAR E.-D, HUYGHE C, JULIER B, and ECALLE C. 2000. Genetic variation for seed yield and its components in alfalfa (Medicago sativa L.) populations.Agronomie 20: 333–345.
  • CEBRAT J. 1973. Cytoembriologiczne badania nad przyczynami niskiej płodności lucerny mieszańcowej (Medicago media Pers.). Zeszyty Problemowe Postępów Nauk Rolniczych 131: 99–100.
  • CHUDZIK B, ZARZYKA B, and ŚNIEŻKO T. 2005. Immunodetection of arabinogalactan proteins in different types of plantovules. Acta Biologica Cracoviensia Series Botanica47(1): 139–146.
  • COOK DR. 1999. Medicago truncatula – a model in the making! Current Opinion in Plant Biology 2: 301–304.
  • DOLIŃSKI R, and HEFNY M. 2006. Regeneracje roślin lucerny mieszańcowej (Medicago sativa L. subsp. falcata xsubsp. sativa) z wierzchołków pędów. Annales UMCS,Sec. E, 61: 63–73.
  • JABŁOŃSKI B. 1973. Badania biologii kwitnienia i zapylenia lucerny mieszańcowej. Pszczelarskie Zeszyty Problemowe14: 1–7.
  • JOHRI BM, AMBEGAOKAR KB, and Srivastava PS. 1992. Comparative Embryology of Angiosperms, vol. 1.Springer-Verlag, Berlin, Heidelberg, New York.
  • KLUCHER KM, CHOW E, REISER L, and FISCHER RL. 1996. The AINTEGUMENTA gene of Arabidopsis required for ovuleand female gametophyte development is related to thefloral homeotic gene APETALA2. Plant Cell 8: 137–153.
  • KOLYASNIKOVA NL. 1985. Determining the fertility of alfalfa by means of fluorescence microscopy. BotanicheskieIssledovaniya na Urale 25.
  • MARTIN FW. 1959. Staining and observing pollen tubes by means of fluorescence. Stain Technology 34: 125–128.
  • PEREIRA TNS., ILARSLAN H, and PALMER RG. 1997. Genetic and cytological analyses of three lethal ovule mutants in soybean(Glycine max; Leguminosae). Genome 40:273–285.
  • ROSELLINI D, LORENZETTI F, and BINGHAM ET. 1998. Quantitative ovule sterility in Medicago sativa.Theoretical and Applied Genetics 97: 1289–1295.
  • STASZEWSKI Z, JAGODZIŃSKA J, JAKUBOWSKA B, and OSIŃSKI R. 1990. Lucerne mutations useable for increasing seedyields. Proc. 9th Eucarpia Meet., Folder Crops Section,18–19.
  • STASZEWSKI Z, STASZEWSKI L, and OSIŃSKI R. 1992. Top flowering – spontaneous mutation of Medicago sativa L. Thefuture of lucerne. Proc. 10th Eucarpia Meet., GroupMedicago, 392–395.
  • ŚNIEŻKO R, and CHUDZIK B. 2003. Zalążek jako aktywny partner w procesie rozmnażania generatywnego roślin kwiatowych.Kosmos 52: 445–457.
  • WOJCIECHOWSKI A, and DYBA S. 1979. Zastosowanie mikroskopu fluorescencyjnego do analizy kiełkowaniałagiewek pyłkowych lucerny (Medicago media Pers.).Hodowla Roślin 2: 14–17.
  • YOUNG BA, SHERWOOD RT, and BASHAW EC. 1979. Cleared-pistil and thick–sectioning techniques for detectingaposporous apomixes in grasses. Canadian Journal ofBotany 57: 1668–1672.

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Bibliografia

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