Uptake and metabolism of the phenylpyridazinone herbicide metflurazon during the bleaching and regeneration process of the green alga,Chlorella fusca

The uptake and metabolism of the pyridazinone herbicide metflurazon by the green alga Chlorella fusca was studied using a new and sensitive technique which is based on reverse-phase high-performance liquid chromatography. During the metflurazon-induced bleaching process, the agent is rapidly taken up and metabolized to the monomethyl derivative, norflurazon, by N-demethylation. Norflurazon accumulates during the treatment in the culture medium because Chlorella cells demethylate norflurazon to the less-phytotoxic SAN 9774 only to a very minor extent. It is shown that only 10% of the initial 1 μM metflurazon is sufficient to induce the bleaching process. This amount is much too small to directly inhibit the photosynthetic electron transport, so that a contribution of this site of action to the bleaching process is not likely. Treated Chlorella cells are able to regenerate to photosynthetically active cells. This phenomenon is based on the inability of the regenerating algae to further take up and demethylate metflurazon. Fully regenerated cells are resistant to metflurazon because a treatment with 1 μM metflurazon neither affects growth nor inhibits photosynthetic activity. This resistance results from an altered permeability of the cell membrane with respect to phenylpyridazinones and an inhibited N-demethylation of metflurazon. These results clearly show that metflurazon itself is nonphytotoxic, and has to be demethylated to norflurazon to exert its bleaching activity.     

Changes in composition of chlorophylls,carotenoids, and prenylquinones in green seedlings of Hordeum and Raphanus induced by the herbicide San 6706—an effect possibly antagonistic to phytochrome action

The substituted pyridazinone herbicide San 6706 (4-chloro-5-(dimethylamino)-2-(α,α,α-trifluoro-m-tolyl)-3-(2H)-pyridazinone) inhibits accumulation of chlorophylls and carotenoids to about the same degree in Hordeum and Raphanus seedlings under continuous illumination. Stronger inhibition of pigment accumulation in general is correlated with a stronger inhibition of the prenylquinones plastoquinone-9,α-tocopherol, and α-tocoquinone; but the amounts of inhibition are much lower for the prenylquinones. Such an inhibition pattern, which is observed in the two plants of different ages and when different herbicide concentrations are applied, points to a site of action which regulates the biosynthesis of these prenyllipids together. There is a different degree in the change of the relative proportions (percentages of herbicide-treated plants as related to the respective control values) of the single carotenoids induced by the herbicide. In this sense there was the highest increase for zeaxanthin and lowest for β-carotene both in Hordeum and Raphanus. The order of relative change of the carotenoids analyzed is about the same as in etiolated barley seedlings of equal age illuminated with white light—but with an opposite sign. The relative proportions of the benzoquinones might be changed in an analogous way. It is suggested, that with respect to carotenoid synthesis and perhaps also benzoquinone synthesis San 6706 acts on the same reaction chain like phytochrome but in an antagonistic way, possibly at the cytoplasmic ribosomes.     

Changes induced by Trichoderma harzianum in suppressive compost controlling Fusarium wilt

The addition of species of Trichoderma to compost is a widespread technique used to control different plant diseases. The biological control activity of these species is mainly attributable to a combination of several mechanisms of action, which may affect the microbiota involved in the suppressiveness of compost. This study was therefore performed to determine the effect of inoculation of Trichoderma harzianum (T. harzianum) on compost, focusing on bacterial community structure (16S rRNA) and chitinase gene diversity. In addition, the ability of vineyard pruning waste compost, amended (GCTh) or not (GC) with T. harzianum, to suppress Fusarium wilt was evaluated. The addition of T. harzianum resulted in a high relative abundance of certain chitinolytic bacteria as well as in remarkable protection against Fusarium oxysporum comparable to that induced by compost GC. Moreover, variations in the abiotic characteristics of the media, such as pH, C, N and iron levels, were observed. Despite the lower diversity of chitinolytic bacteria found in GCTh, the high relative abundance of Streptomyces spp. may be involved in the suppressiveness of this growing media. The higher degree of compost suppressiveness achieved after the addition of T. harzianum may be due not only to its biocontrol ability, but also to changes promoted in both abiotic and biotic characteristics of the growing media.     

The influence of the herbicide methabenzthiazuron on the synthesis of plastidic lipids in Hordeum vulgare seedlings

The herbicide methabenzthiazuron, and inhibitor of the Hill reaction, was applied to Hordeum seeds at the time of sowing, and the greening process under continuous Fluora light was investigated to the age of 13 days. Chlorophyll and xanthophyll contents were increased by methabenzthiazuron relative to the controls, with degrading ratios of chlorophyll a/chlorophyll b and rising xanthophyll/carotene values. The enhanced ratios of chlorophyll a to lipoquinones, like the absolute values, indicate an inhibition of the lipoquinones. These metabolic alterations are similar to those found in shade-adapted leaves. It is suggested, therefore, that inhibition of the photosynthetic electron transport, like deficiency in light of shade leaves, is compensated by metabolic reactions leading to a greater amount of photosystem II with an enhanced accumulation of the light-trapping chlorophylls and carotenoids.     

Purification and characterisation of a family of glutathione transferases with roles in herbicide detoxification in soybean (Glycine max L.); selective enhancement by herbicides and herbicide safeners

Glutathione transferases in soybean (GmGSTs) involved in herbicide detoxification in cell suspension cultures were purified by S-hexylglutathione affinity chromatography and resolved by a combination of HPLC and SDS-PAGE into 11 polypeptides. Analysis by Western blotting using antisera raised to three previously characterised tau (GmGSTU) class subunits demonstrated that five polypeptides were related to GmGSTU1, three to GmGSTU2, and one to Gm GSTU3. Plants contained a simpler profile of polypeptides, with a single GmGSTU2-like polypeptide predominating. With respect to herbicide detoxification, two GmGSTU2-related polypeptides dominated the activity toward the chloroacetanilide acetochlor, while an unclassified subunit was uniquely associated with the detoxification of diphenyl ethers (acifluorfen, fomesafen). The inducibility of the different GST subunits was determined in soybean plants exposed to photobleaching diphenyl ethers and the safeners naphthalic anhydride and dichlormid. GmGSTU3, a GmGSTU1-like polypeptide, and thiol (homoglutathione) content were induced by all chemical treatments, while two uncharacterised subunits were only induced in plants showing photobleaching.     

The origins of selectivity and performance of a new pre-emergence bleaching herbicide,WL 110547. Part I: Factors affecting uptake

A novel compound, 1-(3-trifluoromethylphenyl)-5-phenoxy-1,2,3,4-tetrazole (WL 110547) is a pre-emergence bleaching herbicide with selectivities in certain crops. These selectivities and the weed-control spectrum are derived, in part, from features which influence the uptake of WL 110547 into sensitive tissue. WL 110547 is strongly adsorbed to soil with measured K_oc values in the range 1500-2500 and, following application, is confined to the surface layers of soil, especially when the organic matter content is high. Some plant species have anatomical features which protect their developing leaf tissue from contact with the soil during emergence and thus escape direct contact with these treated layers. Furthermore, some of these plants are deeply rooted and thus there is little opportunity for sufficient uptake of WL 110547 to cause a phytotoxic effect. However some weeds, especially annual dicotyledons, germinate only from shallow depths and, during emergence, their cotyledons or leaves are in contact with the soil. In soils treated with WL 110547 they can thus absorb phytotoxic concentrations of herbicide directly into their cotyledons or leaves. Additional uptake may also occur through roots near the surface and allow WL 110547 to be translocated via the transpiration stream to the site of action in cotyledons and leaves and enhance phytotoxicity. Knowledge of the features controlling uptake, combined with a knowledge of intrinsic susceptibility, have allowed an understanding of the spectrum of weed control and the selectivities between weeds and crops.     

Structure-activity relationships of pheromonostasis induced by ACCase-inhibitor herbicides in the moth Helicoverpa armigera

Many moth sex pheromone blends are derived from fatty acids and their production is regulated by a Pheromone Biosynthesis Activating Neuropeptide (PBAN). In prior work we showed that the herbicide Diclofop-acid, an acetyl-coenzyme A carboxylase (ACCase) inhibitor, inhibits PBAN-induced sex pheromone production in vitro. In this work we extend our study showing that several other herbicides, belonging to the 2-aryloxyphenoxypropionate (‘FOP’) and the cyclohexandione-oxime (‘DIM’) families significantly inhibit pheromone production by adult females whilst survival is unaffected by treatment. Enzyme activity in vitro and kinetic analysis revealed a K_m of 0.35 μM with K_i values of 0.1 and 0.28 μM due to Tralkoxydim and Diclofop inhibition, respectively. Inhibitory activity on PBAN-induced pheromone production by all herbicides tested revealed a potency order: Tralkoxydim > Clodinafop > Cycloxidim > Haloxyfop > Diclofop > Fenoxaprop > Fluazifop > Quizalofop, Quizalofop being inactive. Differences in inhibition efficiencies may be attributed to different binding sites on the enzyme or to the polarity and solubility of these compounds.     

Hemocyanin lipid uptake in Polybetes pythagoricus is altered by fenitrothion

The spider very high density lipoprotein (VHDL), which contains hemocyanin as the major apoprotein, transports most of the circulating lipids. In this work, the effect of the pesticide fenitrothion (FS) on the ability of VHDL-apoproteins to uptake different lipids was investigated. For this, VHDL was delipidated using Triton X-100 and recombined with different radiolabeled lipids in the presence or the absence of FS. The oligomeric structural integrity was maintained after delipidation as shown by non-denaturating PAGE. In the presence of the insecticide, palmitic acid uptake decreased by 28.2 and 62.4% after treating the apolipoprotein with 10 and 20 ppm FS, respectively. Decreases in the uptake of cholesterol, triolein, and phosphatidylcholine caused by FS were 29, 23, and 31% using 10 ppm, and 40, 44, and 29% using 20 ppm FS, respectively. Fluorescence measurements with the hydrophobic probes diphenylhexatriene (DPH) and diphenylhexatrienyl-propionic acid (DPH-PA) indicate that FS induces a red shift, decreases the intensity and increases the anisotropy of the emission of these probes in the VHDL. These results indicate that insecticide binding to the lipoprotein enhances the environment polarity and restricts the mobility of these probes at their binding site. These changes at the hydrophobic VHDL binding sites could lead to the decreased affinity for lipids and hydrophobic ligands. It is inferred that FS could alter the normal lipid exchange between this lipoprotein and tissues.     

Oxidative parameters of Rhamdia quelen in response to commercial herbicide containing clomazone and recovery pattern

In this study, fish Rhamdia quelen, were exposed to different concentrations of herbicide clomazone: 0.0 (control), 0.45 and 0.91 mg L⁻¹. After exposure for 8 days to herbicide, fish were transferred to clean water for a recovery period (8 days). Oxidative stress indicators such as thiobarbituric acid reactive substances (TBARS) levels and protein carbonyl content, as well as antioxidant defenses, such as catalase (CAT), superoxide dismutase (SOD), glutathione S-transferase (GST), ascorbic acid and non-protein thiols levels were studied, using the liver, brain and muscle tissues. Herbicide exposure increased TBARS in muscle and in liver at higher concentration. In liver protein carbonylation increased and catalase activity did not change in fish exposed to herbicide. SOD enhanced in liver at concentration of 0.91 mg L⁻¹. GST, ascorbic acid and non-protein thiols levels increase at both concentrations. At the end of the recovery period the most of the parameters recovered whereas GST and ascorbic acid remain elevated. The present study demonstrates the occurrence of disorders in antioxidant parameters and importance in the assessment of the potential risk of herbicides as clomazone on fish species.     

Effects of herbicides and herbicide analogs on [14C]leucine incorporation by suspension-cultured Solanum nigrum cells

Assays of [¹⁴C]leucine incorporation were used to measure effects of herbicides on suspensioncultured heterotrophic Solanum nigrum cells. Most herbicidal vs. nonherbicidal chemicals in a set of 47 compounds could be distinguished from each other based on their extent of inhibition of leucine incorporation by S. nigrum cells. Herbicides which failed to inhibit leucine incorporation were photosynthetic inhibitors. Both phytotoxic and nonphytotoxic thiocarbamate analogs (as determined by whole-plant studies) tended to inhibit leucine incorporation. It was concluded that the leucine incorporation screen could detect a majority of compounds tested which are herbicidal, and that it may also be useful to detect compounds which have cellular toxicity which is not observed in the whole plant.     

Mutagenic and genotoxic effects of the Atrazine herbicide in Oreochromis niloticus (Perciformes, Cichlidae) detected by the micronuclei test and the comet assay

Atrazine is the triazinic herbicide most found in the rural aquatic environments due to its extensive use and its stability in such places. The mutagenicity and the genotoxicity of different concentrations of the Atrazine herbicide were determinated by the micronucleus test and the comet assay, using Oreochromis niloticus as test-system. The tested concentrations of Atrazine herbicide were 6.25, 12.5 and 25 μg/L, both for the micronuclei test and for the comet assay. The results showed a significant rate of micronuclei and nuclear abnormalities for all the tested concentrations of Atrazine herbicide. For the comet assay, we also observed results significantly different from the control in 6.25, 12.5 and 25 μg/L concentrations. Due to these results, we could infer that such herbicide may be dangerous to the lives of those organisms exposed to it.     

Pyrethroid resistance in a strain of Spodoptera littoralis is correlated with decreased sensitivity of the CNS in vitro

The effects of permethrin and cypermethrin on the isolated abdominal nerve cord of insecticide-resistant [R] and -susceptible [S] strains of Spodoptera littoralis larvae have been studied. Above ca. 19°C, permethrin at 10^?7M caused a prolonged spike train to follow electrical stimulation of the nerve cord. The time of onset of this repetitive firing was significantly greater for the [R] strain. Moreover, cypermethrin, to which this strain shows negligible resistance, did not cause such repetitive discharges. Thus, resistance to permethrin but not to cypermethrin appears to be based on a qualitative difference between the pyrethroids. Nerve blockage by the two pyrethroids was also investigated, with particular reference to temperature. Once again, differences were apparent: when considered relative to untreated controls, permethrin caused quicker nerve blockage as temperature was reduced whereas the blocking action of cypermethrin was not affected by temperature. However, the times taken to cause nerve blockage by permethrin in [R] and [S] larvae were not significantly different, making it unlikely that nerve blockage plays a major role in this resistance. Two methods were employed to reduce the resistance factor in vitro. The synergist dodecyl imidazole failed to significantly reduce the time taken for permethrin to cause either repetitive firing or nerve blockage. However, reducing the calcium concentration in the saline did significantly reduce the latency of repetitive firing caused by permethrin in [R] larvae, thus increasing the nerve sensitivity to approximately the same level as normal calcium, [S] insects.     

Possible involvement of herbicide sequestration in the resistance to diclofop-methyl in Italian biotypes of Lolium spp.

The mechanism of resistance to diclofop-methyl in three Italian populations of Lolium spp. (two resistant and one susceptible) was investigated. The major proportion of R-1 (Tuscania 1997) and R-2 (Roma 1994) plants (approximately 80%) survived after herbicide treatment by emitting new tillers from the crown. Both resistant (R-1 and R-2) and susceptible (Vetralla 1994) Lolium spp. populations were target-site sensitive. No difference in diclofop-methyl absorption by shoots of resistant and susceptible biotypes was observed. At the dose corresponding to 1× the recommended field rate, a relatively higher metabolism was found in R-2 biotype. In contrast, at the doses 2× and 10× the field rate no difference in herbicide metabolism between susceptible and resistant biotypes was observed. At all the three herbicide doses (1×, 2×, and 10× the field rate) 48 h after the treatment (HAT), the total amount of metabolites produced by wheat was more than three times higher than that produced by resistant and susceptible ryegrass biotypes. At the doses 1× and 2× the field rate, the herbicide translocation was different in the susceptible biotypes compared to resistant biotypes. The total amount of the radiolabel found 48 HAT in culm and root was approximately twice in susceptible biotype than in resistant biotypes. Susceptible and resistant ryegrass biotypes differed in the capability of their roots to acidify the external medium. Susceptible biotype acidified the external solution at approximately 6 times the rates of the resistant biotypes. In the present study, the mechanism responsible for resistance in the investigated resistant biotypes was not univocally identified. Indirect evidence supports the possible involvement of herbicide sequestration or immobilization.     

Activation of paraquat in the earthworm Allolobophora chlorotica is mediated by NAD(P)H-cytochrome c reductase activities

This study reports that earthworms, Allolobophora chlorotica, are capable of biotransforming paraquat, a toxic herbicide, resulting in the formation of reactive oxygen species (ROS). We found that in earthworms the reduction of paraquat is mediated by NADPH- and NADH-cytochrome c reductase activities. The formation of superoxide anion (O₂⁻) from the incubation of paraquat with the earthworm extracts was demonstrated by using both Cypridina luciferin analog (CLA) chemiluminescence and the SOD-inhibitable cytochrome c reduction reaction. In addition, in vivo exposure of earthworms to paraquat in solution (24 and 48 h) was performed to investigate whether or not the herbicide affects the levels of the NAD(P)H-cytochrome c reductase activities. Although in vitro NADPH-cytochrome c reductase reduces paraquat more easily than the NADH-dependent activity, after the in vivo exposure an increase of NADH-cytochrome c reductase activity(s) by 12% compared to control values was observed, whereas NADPH-cytochrome c reductase activity was not affected. Xanthine oxidase (XO) is an enzyme implicated in paraquat toxicity, however, no XO was detected in earthworm extracts nor hypoxanthine was a source of electrons for the herbicide reduction. For comparative reasons menadione, a redox cycling quinone, was also incubated with the earthworm extracts. It was found that the incubation of menadione with earthworm extracts formed about two times more (O₂⁻) than with paraquat. It is concluded that the exposure of paraquat to earthworms could elicit radical formation and consequently toxic effects via oxidative stress-mediated mechanisms. The reduction of paraquat by the reductases leads to the formation of paraquat radical, which reacts with molecular oxygen, accounting for the formation of superoxide anion. Further studies are required to conclude that the observed increase of NADH-cytochrome c reductase activity(s) should be used as a biomarker for paraquat exposure in earthworms.     

Ultra-structural changes in the integument induced by the use of three of six forms of allylisothiocyanate tested against Plutella xylostella and Pieris rapae larvae

The insecticidal activity of four forms of Hong Jing (HJ) allylisothiocyanate (AITC), AITC + cypermethrin (HJ_A, HJ_B, and HJ_C) with ratio of (1:1, 4:1, and 2:1), pure AITC (HJ_D), and two forms of Hong Du (HD) AITC, AITC + chlorpyrifos (HD_A and HD_B) with ratio of (2:1 and 2:1), respectively, were studied on the major cruciferous insect larvae Plutella xylostella (L.) and Pieris rapae (L.) by combining both spraying and dipping methods. The P. rapae was more susceptible than P. xylostella larvae. The LC₅₀ values 72 h after treatment of AITC forms (HJ_B, HJ_A, HJ_C, HJ_D, HD_B, and HD_A) on the P. rapae were; 0.07, 0.08, 0.16, 0.83, 0.26, 1.08 gL⁻¹, and 0.69, 0.26, 5.45, 0.93, 3.01, 5.98 gL⁻¹ on the P. xylostella, respectively. The toxicity of some of the AITC forms was very close to or better than that of the commercial contact insecticides such as chlorpyrifos (LC₅₀ = 0.03 and 0.04 gL⁻¹ on P. rapae and P. xylostella, respectively), and cypermethrin (0.65 and 0.78 gL⁻¹, respectively, against P. rapae and P. xylostella). The ultrastructural studies on the integument of the third larval instar of P. xylostella treated by sub-lethal concentration (LC₂₀) of HJ_B, HJ_D, and HD_B were carried out by using transmission electron microscope. The more pronounced alterations in the hypodermis and mitochondria cells. They exhibited changes in all treated samples. The hypodermis was almost completely destroyed, and the mitochondria exhibited morphological alterations, represented by enlargement, matrix rarefaction and vacuolization of the mitochondria matrix, quantity of cristae reduced, and density electron matrix lessened. These AITC forms have potential as contact insecticides, and the ultra structural observations confirm the insecticidal efficiency of different AITC forms on P. rapae and P. xylostella.     

Differential morphological and physiological responses of two oilseed Brassica species to a new herbicide ZJ0273 used in rapeseed fields

Weeds are considered as a major threat to the production of oilseed Brassica crops. The use of herbicides that are safe for crops and effective in controlling weeds is crucial for the agronomists and farmers. Propyl 4-(2-(4,6-dimethoxypyrimidin-2-yloxy)benzylamino)benzoate (ZJ0273), a derivative of 2-pyrimidinyloxy-N-aryl benzoate, is a new herbicide used in the rapeseed field. To evaluate the tolerance of Brassica species against this new herbicide, two cultivars of rapeseed Brassica napus cv. ZS 758 and Brassica rapa cv. Xiaoyoucai were tested by a foliar spray of ZJ0273 at the rate of 100, 500 and 1000 mg/L and a currently used ALS (acetolactate synthase)-inhibiting herbicide bispyribac-sodium (BS) at the rate of 100 mg/L. The results showed that both the cultivars of Brassica were less affected by ZJ0273 as compared to BS. Increasing level of ZJ0273 herbicide from 100 to 1000 mg/L increased the stress for the plants of both the cultivars as indicated by enhanced accumulation of malondialdehyde content. The activities of ALS and antioxidant enzymes (superoxide dismutase and peroxidase), soluble protein and sugar contents, photosynthetic system (SPAD value, photosynthetic rate and chlorophyll fluorescence) as well as the agronomic characters also declined consistently with each successive increase in ZJ0273 concentration. In general, the plants treated with 100 mg/L ZJ0273 recovered from the herbicide stress after 28 days. B. napus showed more tolerance than B. rapa to the new herbicide. Nevertheless, BS application at 100 mg/L did not allow the plants of both the cultivars to recover from the herbicidal stress.     

Evolution of ACCase-inhibitor resistance in Chloris virgata is conferred by a Trp2027Cys mutation in the herbicide target site

BACKGROUND

Chloris virgata is a troublesome weed in tropical regions. With the evolution of glyphosate resistance in key grass species, acetyl CoA carboxylase (ACCase) inhibitors have become a commonly used tool in soybean production areas in Brazil. We assessed if suspected resistant populations exhibited cross resistance to the different classes of ACCase inhibitors and investigated the resistance mechanisms in C. virgata.

RESULTS

Dose–response experiments revealed resistance to haloxyfop-methyl and pinoxaden, with 432- and 3-fold resistance, respectively, compared to susceptible populations. Due to the lack of genetic resources for C. virgata, we sequenced, assembled, and annotated the genome using short-read Illumina technology. The k-mer analysis estimated a genome size of approximately 336 Mbp, with BUSCO completeness of 97%, and over 36 000 gene models were annotated. We examined if ACCase copy number variation and increased gene expression were involved in the resistance phenotype and found no difference when compared to a susceptible population. A mutation was detected in ACCase that encodes for amino acid position 2027, resulting in a tryptophan-to-cysteine (Trp2027Cys) substitution. We found the resistant population absorbed 11.4% less herbicide and retained 21% more herbicide on the treated leaf compared to the susceptible population. We developed a genotyping assay targeting the resistance-endowing Trp2027Cys substitution for quick resistance diagnosis.

CONCLUSION

A Trp2027Cys amino acid substitution in ACCase confers resistance to haloxyfop and pinoxaden in C. virgata. We provide important insights into the evolutionary history of C. virgata and a draft genome as a useful resource to further our understanding of the biology in the genus Chloris. © 2023 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.     

发酵时间和乙二酸前体对小核盘菌生物除草剂致病力的影响

以粉碎的大麦颗粒为培养基,采用固体发酵法制作小核盘菌Sclerotinia minor Jagger生物除草剂,研究发酵时间和乙二酸生物合成前体物质对除草菌的生活力、致病力及乙二酸产量的影响,以期为提高除草菌除草效率提供理论依据.发酵7天的液体菌种生产的除草菌生活力达到最大,为65.0 mm,发酵6天的液体菌种生产的除草菌致病力达到最大,为55.8 mm;固体发酵6天的除草菌的生活力、致病力和乙二酸产量均达到最大,分别为64.3 mm、54.3 mm和0.131 mg/g;添加乙二酸前体对除草菌生活力没有明显影响.添加浓度为56mmol/L的琥珀酸钠和柠檬酸后,除草菌中乙二酸产量分别比对照增加了64.4%和39.7%,除草菌的致病力分别增加了12.4%和5.4%,乙二酸产量与致病力之间存在正相关性.     

Spontaneous ultraweak photon emission from rice (Oryza sativa L.) and paddy weeds treated with a sulfonylurea herbicide

All living organisms spontaneously generate ultraweak photon emissions, which originate from biochemical reactions in cells. Current research uses the ultraweak photon emissions from organisms as a novel tool to investigate the physiological states of plants. In this study, we found ultraweak photon emissions from leaf segments of rice and several paddy weed species treated with a sulfonylurea herbicide. There is a definite difference in photon emissions among plant species, and rice (Oryza sativa), barnyardgrass (Echinochloa crus-galli) and Cyperus serotinus showed extremely strong enhancement of photon emissions. Photon emissions from these three species treated with sulfonylurea herbicide were suppressed when the leaf segments were treated with the cytochrome P450 monooxygenase (P450) inhibitors, piperonyl butoxide and malathion. These results suggest that P450 inhibitors affect the ultraweak photon emissions from plants.     

Calcium entry blockers inhibit contractures induced by the molluscicide Frescon in Lymnaea stagnalis smooth and cross-striated muscles

The molluscicide Frescon induces irreversible contracture in smooth and cross-striated muscles of the freshwater snail Lymnaea stagnalis. This contracture can be inhibited or reversed by elevated Mg²⁺ and reduced Ca²⁺ concentrations, by the heavy metals Ni²⁺, Co²⁺, and Mn²⁺, by the rare earth La³⁺, and by the calcium channel blocker D-600. The removal of extracellular Ca²⁺ also prevents the expression of Frescon action. These results are consistent with the hypothesis that Frescon causes an increase in the Ca²⁺ permeability of the sarcolemma.