Glyphosate induces transient male sterility in Ipomoea purpurea

Plant death is the most common effect resulting from the application of glyphosate, the active ingredient in the herbicide Roundup 1 . Individual seedlings of the morning glory, Ipomoea purpurea L. Roth, however, have been shown to exhibit tolerance to glyphosate, surviving after what should have been a lethal dose. Those that grow and reach reproduc- tive maturity often exhibit deformed anthers within what appear to be normally developed flowers. Ipomoea purpurea has a mixed mating system and normally has hermaphroditic flowers that are capable of both selfing and outcrossing. The de- formed anthers do not produce pollen, essentially converting a hermaphroditic flower to a female. Here we describe this morphological change and investigate the reproductive consequences of anther deformation. First, there is phenotypic var- iation for the propensity of an individual to exhibit male sterility through deformed anthers in response to treatment, but a series of field and greenhouse studies suggest that this variation is not genetic. The male sterility is also transient; within an individual, the frequency of flowers with deformed anthers declines over time. Although flowers with deformed anthers do not produce pollen, we observed mixed effects on female function of such flowers. In the greenhouse, flowers with de- formed anthers that were hand-pollinated produced as many seeds as flowers with normal anthers, suggesting no effect on female fertility. In the field, however, plants with a higher proportion of anther deformation set significantly fewer seeds than those untreated, suggesting either reduced female fertility, or a reproductive penalty in flowers with deformed anthers due to the inability to self pollinate. Thus, the presence of this trait could alter the selfing to outcrossing ratio in popula- tions that are sprayed with the herbicide. Individuals that exhibited a higher proportion of anther deformation also produce fewer total flowers than untreated plants, suggesting that anther deformation is part of a suite of responses to damage by glyphosate.

[1]  R. Baucom,et al.  The evolution of novel herbicide tolerance in a noxious weed: the geographic mosaic of selection , 2007, Evolutionary Ecology.

[2]  Stephen O Duke,et al.  The current status and environmental impacts of glyphosate-resistant crops: a review. , 2006, Journal of environmental quality.

[3]  B. Young,et al.  Changes in Herbicide Use Patterns and Production Practices Resulting from Glyphosate-Resistant Crops1 , 2006, Weed Technology.

[4]  R. Relyea The Lethal Impacts of Roundup and Predatory Stress on Six Species of North American Tadpoles , 2005, Archives of environmental contamination and toxicology.

[5]  R. Baucom,et al.  Fitness costs and benefits of novel herbicide tolerance in a noxious weed. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[6]  Judith F. Thomas,et al.  Glyphosate negatively affects pollen viability but not pollination and seed set in glyphosate-resistant corn , 2004, Weed Science.

[7]  R. Ennos Quantitative studies of the mating system in two sympatric species of Ipomoea (Convolvulaceae) , 1981, Genetica.

[8]  S. Senseman,et al.  Boll Abscission Responses of Glyphosate-Resistant Cotton (Gossypium hirsutum) to Glyphosate1 , 2003, Weed Technology.

[9]  Judith F. Thomas,et al.  Glyphosate-induced reductions in pollen viability and seed set in glyphosate-resistant cotton and attempted remediation by gibberellic acid (GA3) , 2003, Weed Science.

[10]  Judith F. Thomas,et al.  Reproductive abnormalities in glyphosate-resistant cotton caused by lower CP4-EPSPS levels in the male reproductive tissue , 2002, Weed Science.

[11]  M. Rausher,et al.  Frequency‐Dependent Pollen Discounting Contributes to Maintenance of a Mixed Mating System in the Common Morning Glory Ipomoea purpurea , 1998, The American Naturalist.

[12]  H. Saini Effects of water stress on male gametophyte development in plants , 1997, Sexual Plant Reproduction.

[13]  David W. Inouye,et al.  Techniques for Pollination Biologists , 1993 .

[14]  D. Roach,et al.  MATERNAL EFFECTS IN PLANTS , 1987 .

[15]  D. Geiger,et al.  Uptake and distribution of N-phosphonomethylglycine in sugar beet plants. , 1981, Plant physiology.