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Bekir Bukun

Researcher at Colorado State University

Publications -  7
Citations -  883

Bekir Bukun is an academic researcher from Colorado State University. The author has contributed to research in topics: Aminopyralid & Aminocyclopyrachlor. The author has an hindex of 7, co-authored 7 publications receiving 783 citations.

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Gene amplification confers glyphosate resistance in Amaranthus palmeri

TL;DR: This work investigated recently discovered glyphosate-resistant Amaranthus palmeri populations from Georgia, in comparison with normally sensitive populations, and revealed that EPSPS genes were present on every chromosome and, therefore, gene amplification was likely not caused by unequal chromosome crossing over.
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Interspecific hybridization transfers a previously unknown glyphosate resistance mechanism in Amaranthus species.

TL;DR: A previously unknown glyphosate resistance mechanism, amplification of the 5‐enolpyruvyl shikimate‐3‐phosphate synthase gene, was recently reported in Amaranthus palmeri, representing an avenue for acquisition of a novel adaptive trait.
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Vapor Movement of Synthetic Auxin Herbicides: Aminocyclopyrachlor, Aminocyclopyrachlor-Methyl Ester, Dicamba, and Aminopyralid

TL;DR: Phytotoxic responses of plants exposed to vapors emanating from various surfaces treated with aminocyclopyrachlor-methyl ester were similar to responses to dicamba under enclosed incubation conditions, but were less in outdoor, open-air environments.
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Absorption and Translocation of Aminocyclopyrachlor and Aminocyclopyrachlor-Methyl Ester in Canada Thistle (Cirsium arvense)

TL;DR: Significantly greater aminocyclopyrachlor-methyl ester was absorbed, compared with the free acid, which was reflected in the greater aboveground translocation for the methyl ester and, based on this conversion rate, was translocated as the free acids in Canada thistle.
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Aminopyralid and Clopyralid Absorption and Translocation in Canada Thistle (Cirsium arvense)

TL;DR: The results suggest that aminopyralid's chemical structure may provide for greater biological activity at the target site than clopyralids.