Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-04T21:45:02.007Z Has data issue: false hasContentIssue false

Pollen-mediated gene flow in wild oat

Published online by Cambridge University Press:  20 January 2017

Bruce G. Murray
Affiliation:
Dow AgroSciences, 104-111 Research Drive, Innovation Place, Saskatoon, Saskatchewan, Canada S7N 3R2
Ian N. Morrison
Affiliation:
Faculty of Agriculture, Forestry and Home Economics, 2-14 Agriculture-Forestry Centre, University of Alberta, Edmonton, Alberta, Canada T6G 2P5

Abstract

Two separate field experiments were conducted to quantify the degree of plant-to-plant outcrossing and pollen-mediated gene flow (PMGF) in wild oat. The purpose of the study was to determine the extent to which pollen movement could contribute to the spread of herbicide resistance in this species. In both experiments, an acetyl-CoA carboxylase inhibitor–resistant (R) wild oat genotype (UM1) was used as the pollen donor and a susceptible (S) genotype (UM5) was used as the pollen receptor. Hybrid progeny resulting from a cross between UM1 and UM5 were identified using the herbicide resistance trait as a marker. In the plant-to-plant outcrossing experiment, single UM5 plants were closely surrounded by 20 homozygous R UM1 plants in hills. By screening seed from the S parent for resistance, outcrossing was determined to range from 0 to 12.3%, with a mean of 5.2% over 10 hills. In the PMGF experiment, single homozygous R UM1 plants were surrounded by UM5 plants arranged in a hexagonal pattern at low and high densities (total of 19 and 37 wild oat plants m−2), growing within spring wheat and flax crops. In the wheat crop, mean wild oat outcrossing was 0.08 and 0.05% at low and high densities, respectively. In the less competitive flax, corresponding outcrossing values were 0.07 and 0.16% at low and high densities, respectively. Distance from the pollen source was a significant factor only for the high-density planting arrangement in flax. Up to 77 R hybrid seeds were recovered from 6 m2 in the PMGF experiment, indicating that PMGF contributes to the evolution of resistance in wild oat populations. However, the contribution of pollen movement to resistance evolution and the spread of resistance in wild oat populations would be relatively small when compared with R seed production and dispersal from a resistant plant.

EDITOR'S NOTE: This manuscript was reviewed by six colleagues whose recommendations varied widely. Lack of repetition was a major concern. The authors address the problem in the last paragraph of the results section. Factors favoring publication included the worldwide importance of wild oats, the minimal data on gene flow in the species, and the fact that the results are consistent with those of other studies cited in this manuscript. The points raised by reviewers who did not favor publication, especially the role of the environment in pollen production and viability, are acknowledged.

R. L. Zimdahl, Editor

Type
Research Article
Copyright
Copyright © Weed Science Society of America 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Literature Cited

Bickelman, U. and Leist, N. 1988. Homogeneity of oat cultivars with respect to outcrossing. Pages 358363 In Proceedings of the 3rd International Oat Conference. Lund, Sweden.Google Scholar
Coffman, F. A. and Wiebe, G. A. 1930. Unusual crossing in oats in Aberdeen, Idaho. J. Am. Soc. Agron. 22:245250.CrossRefGoogle Scholar
Derrick, R. A. 1933. Natural crossing with wild oats, Avena fatua . Sci. Agric. 13:458459.Google Scholar
Eber, F., Chèvre, A. M., Baranger, A., Vallée, P., Tanguy, X., and Renard, M. 1994. Spontaneous hybridization between a male-sterile oilseed rape and two weeds. Theor. Appl. Genet. 88:362368.CrossRefGoogle ScholarPubMed
Gomez, K. A. and Gomez, A. A. 1984. Statistical Procedures for Agricultural Research. 2nd ed. New York: J. Wiley. pp. 187207.Google Scholar
Handel, S. N. 1983. Pollination ecology, plant population structure and gene flow. Pages 163211 In Real, L., ed. Pollination Biology. Orlando, FL: Academic Press.CrossRefGoogle Scholar
Harrington, J. B. 1932. Natural crossing in wheat, oats, and barley at Saskatoon, Saskatchewan. Sci. Agric. 12:470483.Google Scholar
Heap, I. M., Murray, B. G., Loeppky, H. A., and Morrison, I. N. 1993. Resistance to aryloxyphenoxypropionate and cyclohexanedione herbicides in wild oat (Avena fatua). Weed Sci. 41:232238.CrossRefGoogle Scholar
Imam, A. G. and Allard, R. W. 1965. Population studies in predominantly self-pollinated species. VI. Genetic variability between and within natural populations of wild oats from differing habitats in California. Genetics 51:4962.Google ScholarPubMed
Jasieniuk, M., Brûlé-Babel, A. L., and Morrison, I. N. 1996. The evolution and genetics of herbicide resistance in weeds. Weed Sci. 44:176193.CrossRefGoogle Scholar
Levin, D. A. and Kerster, H. W. 1974. Gene flow in seed plants. Pages 139220 In Dobzhansky, T., Hecht, M. K., and Steere, W. C., eds. Evolutionary Biology. Volume 7. New York: Plenum Press.CrossRefGoogle Scholar
Manasse, R. 1992. Ecological risk of transgenic plants: effects of spacial dispersion on gene flow. Ecol. Appl. 2:431438.CrossRefGoogle Scholar
Manasse, R. and Kareiva, P. 1991. Quantifying the spread of recombinant genes and organisms. Pages 215231 In Ginzburg, L., ed. Assessing Ecological Risks of Biotechnology. Boston, MA: Butterworth-Heinemann.CrossRefGoogle Scholar
Maxwell, B. D., Rousch, M. L., and Radosevich, S. R. 1990. Predicting the evolution and dynamics of herbicide resistance in weed populations. Weed Technol. 4:213.CrossRefGoogle Scholar
Morse, P. M. and Thompson, B. K. 1981. Presentation of experimental results. Can. J. Plant Sci. 61:799802.Google Scholar
Murray, B. G., Friesen, L. F., Beaulieu, K. J., and Morrison, I. N. 1996. A seed bioassay to identify acetyl-CoA carboxylase inhibitor resistant wild oat (Avena fatua) populations. Weed Technol. 10:8589.CrossRefGoogle Scholar
Murray, B. G., Morrison, I. N., and Brûlé-Babel, A. L. 1995. Inheritance of acetyl-CoA carboxylase inhibitor resistance in wild oat (Avena fatua). Weed Sci. 43:233238.CrossRefGoogle Scholar
Nurminiemi, M., Tufto, J., Nilsson, N., and Rognli, O. A. 1998. Spatial models of pollen dispersal in the forage grass meadow fescue. Evol. Ecol. 12:487502.CrossRefGoogle Scholar
Scheffler, J. A., Parkinson, R., and Dale, P. J. 1993. Frequency and distance of pollen dispersal from transgenic oilseed rape (Brassica napus). Transgenic Res. 2:356364.CrossRefGoogle Scholar
Slatkin, M. 1985. Gene flow in natural populations. Annu. Rev. Ecol. Syst. 16:393430.CrossRefGoogle Scholar
Smyth, C. A. and Hamrick, J. L. 1987. Realized gene flow via pollen in artificial populations of musk melon, Carduus nutans L. Evolution 41:613619.CrossRefGoogle Scholar