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Background: A Chenopodium album L. biotype surviving in atrazine-treated Serbian corn fields (VC) was compared against atrazine-susceptible (S) and atrazine-resistant (R) standards., Results: Atrazine (2 kg ha(-1)) killed S and VC shoot biomass 15 days after treatment (DAT), but R was only suppressed by 42% and survived 8 kg ha(-1). Atrazine at 2 kg ha(-1) only inhibited VC height by 60% as against 100 and 0% for S and R respectively. Chlorophyll fluorescence (Fv/Fm) and transpiration were insensitive to atrazine in R, but were inhibited by 90 and 100% in S and by 50 and 60% in VC respectively. Decline of Fv/Fm after 2 kg ha(-1) atrazine was stabilized at 3 DAT for the VC biotype., Conclusion: A toxicity mitigation mechanism could have facilitated VC survival in an atrazine-treated field. Further knowledge on this mechanism is needed to establish if surviving VC plants are indicators of atrazine resistance evolution in these Serbian corn fields. Variables related to foliar function provided better detection of weed mechanisms to survive herbicide action than the usual shoot biomass measurements.

The effect of 2-benzylamino-1,3,5-triazines on photosynthetic electron transport (PET) was measured with thylakoids isolated from atrazine-resistant, wild-type Chenopodium album, and spinach to find novel 1,3,5-triazine herbicides bearing a strong PET inhibition. The PET inhibition assay with Chenopodium (wild-type and resistant), yielded a resistance ratio (R/W = I50 (resistant)/I50 (wild-type)) of 324 for atrazine while for benzylamino-1,3,5-triazine derivatives of diamino-1,3,5-triazines a R/W of 11 to 160 was found. The compounds having a benzylamino group at one of the amino groups in the diamino-1,3,5-triazines have a resistant ratio down to one half to 1/30 of the atrazine value. The average resistance ratio of 21 benzylamino derivatives of monoamino-1,3,5-triazines was found to be about 4.0. The inhibition of 21 benzylamino-1,3,5-triazines assayed with atrazine-resistant Chenopodium thylakoids, indicated by pI50 (R)-values, correlated well with the PET inhibition pI50 (W) of wild-type thylakoids from Chenopodium.