Ultrastructural changes in leaf and needle segments treated with herbicides containing picloram

The herbicide Tordon 50D (picloram+2,4-D) affected the integrity of the nucleus and cell membranes in Pinus radiata needle segments and caused the swelling of internal chloro plast membranes and the eventual disintegration of the chloroplasts. Tordon 22K (picloram) only affected chloro plast structure. Both herbicides had similar adverse effects on cell membranes and chloroplasts of Eucalyptus viminalis.     

The effect of soil aggregate size and water content on herbicide concentration in soil water

Suspensions of wettable powders of metribuzin and simazine were sprayed onto samples of two soils of two particle size grades, > 2.5 mm and <0.5 mm. The soils were either air-dry or at a water content of 12%. After either 1 h or 1 week, water was added to give a soil to water ratio of 1:1. Samples of solution were analysed after 1, 24 and 48 h. With metribuzin the intial concentration for both soils after wetting was greater from the >2.5 mm samples than the <0.5 mm samples, following application to dry soil, but by 48 h the differences were negligible. With simazine WRO soil did not show this effect at all and with Kirton soil only small differences were seen. If the soil was wet at the time of application, particle size had no effect except with simazine in Kirton soil. Generally metribuzin concentrations were higher after application to wet than to dry soils for at least 24 h after wetting whereas simazine concentrations were higher from initially dry soils and the differences had virtually disappeared 24 h after wetting. With the WRO soil herbicide concentrations in soil water were higher if the soil was wetted 1 h after spraying than if left for 1 week but the differences rarely persisted for 48 h. No such trend was observed with Kirton soil. It is concluded that the differences observed in these experiments could be responsible for variations in the performance of soil-applied herbicides.     

The selectivity of methabenzthiazuron between barley, perennial ryegrass and Poa trivialis

In field experiments methabenzthiazuron at 1.1 kg ai/ha applied pre-emergence gave good control of Poa trivialis L. in perennial ryegrass S23 which was undersown in spring barley (Zephyr); no significant damage to barley or perennial ryegrass resulted from 2.2 kg ai/ha. However this dose applied when barley had three to four leaves decreased the subsequent barley yield. In pot experiments in the glasshouse methabenzthiazuron was active mainly due to uptake through the soil. Much greater damage to barley and perennial ryegrass resulted when herbicide-treated soil was placed below seed level than above the seed. The difference was less marked with P. trivialis. The latter started to develop secondary roots near the soil surface earlier than either perennial ryegrass or spring barley.     

Structure-activity relationships of 1,2,3-benzothiadiazoles as synergists for carbaryl against the house fly (Musca domestica)

Fifty six 1,2,3-benzothiadiazoles and related compounds were evaluated as carbaryl synergists against the house fly (Musca domestica). Many of these were excellent synergists, the most active being those containing various combinations of halogen, alkyl, or alkoxy substituents in the 5- and/or 6-positions of the ring.Regression analysis on the data from 14 compounds for which substituents constants were available established that synergistic activity can be satisfactorily described by equations in terms of the hydrophobic bonding constant (π) and the homolytic free radical constant (σ ·).The results with compounds related to the 1,2,3-benzothiadiazoles suggest that synergistic activity is associated primarily with the diazosulfide moiety.     

The effect of phosphine on the absorption and circular dichroic spectra of cytochrome c and cytochrome oxidase

The interaction of phosphine with purified cytochrome c and cytochrome oxidase was studied by absorption and circular dichroic spectrometry. Treatment of cytochrome oxidase with phosphine yielded absorption spectra in both the visible and Soret region that were similar to that produced by dithionite. Striking changes in the circular dichroic spectra were also recorded, sugesting that a valence change of the heme iron was accompanied by a conformation change of the prosthetic group.Phosphine treatment of cytochrome c also yielded spectra similar to those produced by reduction with dithionite suggesting a valence change of the heme iron. However, both the time necessary for complete reduction and the concentration of phosphine necessary for this effect suggest that, in comparison with cytochrome oxidase, cytochrome c was relatively insensitive. Reduction of cytochrome oxidase by phosphine had only a very minor effect on the intrinsic dichroic spectrum suggesting little effect on the polypeptide chains.The persistence of a component after reduction by phosphine and the subsequent reduction of this component by dithionite suggests that phosphine primarily reduced only one comonent of the cytochrome aa₃ complex. The failure of EDTA and fluoride, which are known ligands of cytochrome a₃ to affect the reduction of cytochrome aa₃ by phosphine, as well as the occurrence of a 436-nm isosbestic point of the ferric-ferrous absorption spectra suggests that phosphine reduced primarily cytochrome a. However, it is argued that a slow reduction of cytochrome a₃ cannot be ruled out.     

Isomerization and Beckmann rearrangement reactions in the metabolism of methomyl in rats

Methomyl {S-methyl-N-[(methylcarbamoyl)oxy]thioacetimidate}, also known as Lannate, may exist in two geometric configurations but the more stable syn isomer is the form applied as an insecticide. In the rat, syn[¹⁴CN]methomyl [CH₃S(CH₃)CNOC(O)NHCH₃] was metabolized to respiratory ¹⁴CO₂ and $\text{CH}{}_3{}^{14}\text{CN}$ in a ratio of about 2 to 1. Studies with the anti isomer showed that it was metabolized predominately to $\text{CH}{}_3{}^{14}\text{CN}$. These and other data are presented supporting the contention that syn methomyl is partially isomerized to the anti isomer in the animal prior to the hydrolysis of the ester linkage. After hydrolysis, the syn oxime [CH₃S(CH₃)¹⁴CNOH] is further metabolized to ¹⁴CO₂ while the anti oxime is metabolized to $\text{CH}{}_3{}^{14}\text{CN}$. Proposed immediate precursors to the carbon dioxide and acetonitrile, formed by Beckmann rearrangement of the syn and anti oximes, are CH₃S¹⁴C(O)NHCH₃ and $\text{[}\text{CH}{}_3{}^{\mathrm{14\oplus }}\text{CNSCH}{}_3\text{]x}{}^{\mathrm{?}}$, respectively.     

Distinguishing between carbamate and organophosphate insecticide poisoning in house flies by symptomology

Three criteria, latency to convulsions, still period, and recovery are used to distinguish between carbamate and phosphate insecticide poisoning in house flies, Musca domestica. Because of shorter latencies with carbamate-treated flies, the central nervous system was considered more sensitive to the presence of carbamates than phosphates. Recovery from carbamate-induced tetany was considered correlated with reactivation of carbamylated cholinesterase. There appeared to be a fundamental difference between the insecticidal actions of carbamates and phosphates not wholly explainable by cholinesterase inhibition. Tethered or held house flies were less susceptible to poisoning than unrestrained flies.     

Spectral interactions of insecticide synergists with microsomal cytochrome P-450 from insecticide-resistant and susceptible house flies

The spectral interactions of 45 insecticide synergists and related compounds with oxidized and reduced cytochrome P-450 from microsomes of insecticide-resistant and -susceptible house flies were investigated. The type III interaction typical of piperonyl butoxide was the most common spectral interaction for the compounds studied. In addition to this, several other varients of the type III interaction were noted. In general these responses with house fly microsomes were similar to those reported for mammals, although some minor species and strain differences were observed. The cytochrome P-450 from susceptible house flies, although reported previously not to exhibit type I difference spectra with many xenobiotics, was found to elicit this spectral response with several methylenedioxyphenyl compounds.     

Biochemical genetics of oxidative resistance to diazinon in the house fly

The genetics and biochemistry of oxidative resistance to diazinon were investigated in a diazinon-resistant strain of the house fly, Musca domestica L. The resistant strain was crossed with a multimarker susceptible strain and substrains containing portions of the resistant strain genome were prepared. Resistance, microsomal oxidase, and cytochrome P-450 spectral characteristics were then compared in the different strains. The major gene for resistance to diazinon is semidominant and is located on chromosome II, 13 crossing over units from the recessive mutant stubby wing. Additional resistance genes occur on chromosome II and on other chromosomes as well. Resistance to diazinon was introduced into a susceptible mutant-marked strain via genetic crossing over. Increases in parathion oxidase, total and P-450-specific N- and O-demethylase activity, and resistant strain type I binding spectrum were introduced along with resistance, indicating genes controlling these parameters and resistance are either identical or closely linked. No increase in activity of cytochrome P-450 itself was introduced into the mutant strain. Additional genes controlling the amount of cytochrome P-450 and several spectral changes characteristic of the resistant strains are apparently controlled by genes located at different loci on chromosome II. Resistance factors on other chromosomes are also present, but were not characterized.