Impact of field dodder (Cuscuta campestris Yunk.) on physiological and anatomical changes in untreated and herbicide-treated alfalfa plants

  • Marija M Sarić-Krsmanović Institute of Pesticides and Environmental Protection, Banatska 31b, 11080 Belgrade
  • Dragana Božić University of Belgrade, Faculty of Agriculture, Nemanjina 6, 11080 Belgrade
  • Ljiljana Radivojević Institute of Pesticides and Environmental Protection, Banatska 31b, 11080 Belgrade
  • Jelena Gajić Umiljendić Institute of Pesticides and Environmental Protection, Banatska 31b, 11080 Belgrade
  • Sava Vrbničanin University of Belgrade, Faculty of Agriculture, Nemanjina 6, 11080 Belgrade
Keywords: Field dodder, Alfalfa, Herbicide, Pigments, Anatomical parameters,

Abstract


The effects of field dodder on physiological processes and the anatomy of alfalfa plants were examined under controlled conditions. The experiment included the following variants: N - noninfested alfalfa plants (control); I - infested alfalfa plants (untreated); T - infested plants treated with imazethapyr. Imazethapyr application rate was 100 g a.i. ha-1. The following parameters were checked: physiological - pigment content (chlorophyll a, chlorophyll b, total carotenoids); anatomical - stem parameters: thickness of epidermis and cortex, and diameter of stem and central cylinder; leaf parameters: thickness of epidermis, parenchyma and spongy tissue, mesophyll and underside leaf epidermis, and diameter of bundle sheath cells in alfalfa plants. Pigment contents and anatomical parameters were measured: prior to herbicide treatment (0 assessment), then 7 (I assessment), 14 (II assessment), 21 (III assessment), 28 (IV assessment) and 35 (V assessment) days after application (DAA).
Field dodder was found to affect the contents of chlorophyll a, chlorophyll a and carotenoids in untreated alfalfa plants, causing significant reductions in pigment content.
Conversely, percent reduction in the treated plants decreased 22-5% for chlorophyll a, 25-1%, for chlorophyll b, and 21-11% for carotenoids, while a stimulating effect of 1-6% was observed for the contents of chlorophyll b and carotenoids 35 DAA. Plants infested (untreated) by field dodder had lower values of most anatomical parameters, compared to noninfested plants. The measured anatomical parameters of alfalfa stems and leaves had significantly higher values in noninfested plants and plants treated with imazethapyr than in untreated plants.

Author Biographies

Marija M Sarić-Krsmanović, Institute of Pesticides and Environmental Protection, Banatska 31b, 11080 Belgrade
Research Associate
Dragana Božić, University of Belgrade, Faculty of Agriculture, Nemanjina 6, 11080 Belgrade
Assistant Professor
Ljiljana Radivojević, Institute of Pesticides and Environmental Protection, Banatska 31b, 11080 Belgrade
Senior Research Associate
Jelena Gajić Umiljendić, Institute of Pesticides and Environmental Protection, Banatska 31b, 11080 Belgrade
Research Associate
Sava Vrbničanin, University of Belgrade, Faculty of Agriculture, Nemanjina 6, 11080 Belgrade
Professor

References

Berg, S., Krupinska, K., & Krause, K. (2003). Plastids of three Cuscuta species differing in plastid coding capacity have a common parasite-specific RNA composition. Planta, 218(1), 135-142. pmid:12898255. doi:10.1007/s00425-003-1082-8

Cudney, D.W., Orloff, S.B., & Reints, J.S. (1992). An integrated weed management procedure for the control of dodder (Cuscuta indecora) in alfalfa (Medicago sativa). Weed Technology, 6(3), 603-606.

Dawson, J.H., Musselman, L.J., Wolswinkel, P., & Dörr, I. (1994). Biology and control of Cuscuta. Reviews of Weed Science, 6, 265-317.

Fathoulla, C.N., & Duhoky, M.M.S. (2008). Biological and anatomical study of different Cuscuta species (Kurdistan 1st Conference on Biological Sciences). Journal of Dohuk University, 11(1), 22-39.

Funk, H.T., Berg, S., Krupinska, K., Maier, U.G., & Krause, K. (2007). Complete DNA sequences of the plastid genomes of two parasitic flowering plant species, Cuscuta reflexa and Cuscuta gronovii. BMC Plant Biology, 7(1), 45. doi: 10.1186/1471-2229-7-45

García, M.A., Costea, M., Kuzmina, M. & Stefanović, S. (2014). Phylogeny, character evolution, and biogeography of Cuscuta (dodders; Convolvulaceae) inferred from coding plastid and nuclear sequences. American Journal of Botany, 101(4), 670-690. doi:10.3732/ajb.1300449

Hibberd, J.M., Bungard, R.A., Press, M.C., Jeschke, W.D., Scholes, J.D., & Quick, W.P. (1998). Localization of photosynthetic metabolism in the parasitic angiosperm Cuscuta reflexa. Planta, 205(4), 506-513. doi: 10.1007/s004250050349

Hibberd, J.M., & Jeschke, W.D. (2001). Solute flux into parasitic plants. Journal of Experimental Botany, 52, 2043-2049. doi: 10.1093/jexbot/52.363.2043

Joel, D.M., Hershenhorn, J., Eizenberg, H., Aly, R., Ejeta, G., Rich, P.J., … Rubiales, D. (2007). Biology and management of weedy root parasites. Horticultural Reviews, 33, 267-349.

Koskela, T., Salonen, V., & Mutikainen, P. (2001). Interaction of a host plant and its holoparasite: Effects of previous selection by the parasite. Journal of Evolutionary Biology, 14(6), 910-917.

Lichtenthaler, H.K. & Wellburn, A.R. (1983). Determinations of total carotenoides and chlorophylls a and b of leaf extracts in different solvents. Biochemical Society Transactions, 11(5), 591-592. doi: 10.1042/bst0110591

McNeal, J.R., Arumugunathan, K., Kuehl, J.V., Boore, J.L., & de Pamphilis, C.W. (2007a). Systematics and plastid genome evolution of the cryptically photosynthetic parasitic plant genus Cuscuta (Convolvulaceae). BMC Biology, 5, 55. doi: 10.1186/1741-7007-5-55

McNeal, J.R., Kuehl, J.V., Boore, J.L., & de Pamphilis, C.W. (2007b). Complete plastid genome sequences suggest strong selection for retention of photosynthetic genes in the parasitic plant genus Cuscuta. BMC Plant Biology, 7, 57. doi: 10.1186/1471-2229-7-57

Mishra, J.S. (2009): Biology and management of Cuscuta species. Indian Journal of Weed Science, 41(1-2), 1-11.

Panetta, F.D., & Lawes, R. (2005). Evaluation of weed eradication programs: The delimitation of extent. Diversity and Distribution, 11(5), 435-442. doi:10.1111/j.1366-9516.2005.00179.x

Parker, C. (2009). Observations on the current status of Orobanche and Striga problems worldwide. Pest Management Science, 65(5), 453-459.

Ruzin, S.E. (1999). Plant Microtechnique and Microscopy (p 321). New York, NY: Oxford University Press.

Salimi, H. (2000). A study on comparison of seed dormancy and germination in three species of dodder. Rostaniha, 1(4), 33-35.

Stojanović, D., & Mijatović, K. (1973): Distribution, biology and control of Cuscuta spp. in Yugoslavia. In EWRS Symposium on Parasitic Weeds, Malta (pp 269-279). Doorwerth, NL: EWRS.

Van der Kooij, T.A., Krupinska, K., & Krause, K. (2005). Tocochromanol content and composition in different species of the parasitic flowering plant genus Cuscuta. Journal of Plant Physiology, 162, 777-781.

Wellburn, A.R. (1994). The spectral determination of chlorophylls a and b, as well as total carotenoids, using various solvents with spectrophotometers of different resolution. Journal of Plant Physiology, 144(3), 307-313.

Westwood, J.H., Yoder, J.I., Timko, M.P. & de Pamphilis, C. W. (2010). The evolution of parasitism in plants. Trends Plant Science, 15(4), 227-235. doi: 10.1016/j.tplants.2010.01.004

Published
2017/02/03
Section
Original Scientific Paper