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dc.contributor.advisorMerkle, Morris G.
dc.creatorVaughn, Steven Francis
dc.date.accessioned2020-08-21T22:17:00Z
dc.date.available2020-08-21T22:17:00Z
dc.date.issued1987
dc.identifier.urihttps://hdl.handle.net/1969.1/DISSERTATIONS-754602
dc.descriptionTypescript (photocopy).en
dc.description.abstractThe effects of the grass-specific herbicide haloxyfop {2- [4- [[3-chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]-phenoxy]propanoic acid} on the growth and ultrastructure of susceptible sorghum (Sorghum bicolor (L.) Moench.) root meristems were determined. Mitotic index analysis indicated that 1.0 μM haloxyfop inhibited cell division completely after 24 h, and arrested chromosomes in a state similar to prometaphase. Ultrastructural analysis indicated that after 4 h cells treated with 1.0 μM haloxyfop exhibited increased vacuolization, and by 24 h cells contained large vacuoles, some of which were autophagic. Complete cell destruction occurred at the 1.0 μM level by 72 h treatment time. The phytotoxicity of haloxyfop was not altered by the presence of either 2,4-DB [4-(2,4-dichlorophenoxy)butanoic acid] or TIBA (2,3,5-triicdobenzoic acid), though both compounds caused independent effects of their own, e.g. cortical cell expansion, extensive root hair development. These results suggest that a possible mechanism of action of haloxyfop is to cause premature cell differentiation, indicated by extensive vacuolization of meristematic cells, after which intracellular digestion, and subsequent death of the cells take place. Similar, although not identical results were obtained when sorghum roots were treated with the herbicides cinmethylin {exo-1-methyl-4-(1-methylethyl)-2-[(2-methylphenyl)methoxy]-7-oxabicyclo[2.2.1]heptane}, dalapon (2,2-dichloropropanoic acid), and sethoxydim {2-[1-(ethoxyimino)butyl]- 5-[2-(ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one}. These results are also similar those found in research concerning bensulide {0,0- bis(1-methylethyl) S-[2[-(phenylsulfonyl)amino]ethyl]phosphorodithioate), bromacil [5-bromo-6-methyl-3-(1-methylpropyl)-2,4(1H,3H) pyrimidinedione}, isoxaben {N-[3-(1-ethyl-1-methylpropyl)-5-isoxazolyl]-2,6- dimethoxybenzamide}, and propham (1-methylethyl phenylcarbamate), herbicides which have different selectivity among plants and are not chemicallt related. Based upon the data from this research and research with herbicides producing similar effects, two possible mechanisms of action for haloxyfop are proposed.en
dc.format.extentxi, 88 leavesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.rightsThis thesis was part of a retrospective digitization project authorized by the Texas A&M University Libraries. Copyright remains vested with the author(s). It is the user's responsibility to secure permission from the copyright holder(s) for re-use of the work beyond the provision of Fair Use.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectMajor agronomyen
dc.subject.classification1987 Dissertation V317
dc.subject.lcshPlantsen
dc.subject.lcshEffect of herbicides onen
dc.subject.lcshSorghumen
dc.subject.lcshRootsen
dc.subject.lcshHerbicidesen
dc.subject.lcshToxicologyen
dc.titleEffects of haloxyfop on sorghum (Sorghum bicolor (L.) Moench.) root meristemsen
dc.typeThesisen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.namePh. Den
dc.contributor.committeeMemberChandler, James M.
dc.contributor.committeeMemberCraile, Harry
dc.contributor.committeeMemberNewton, Ronald J.
dc.type.genredissertationsen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen
dc.publisher.digitalTexas A&M University. Libraries
dc.identifier.oclc18974401


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