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BACKGROUND Ginger (Zingiber officinale Roscoe) is widely planted around the world. Owing to continuous planting, ginger is seriously affected by soilborne fungi, bacteria, and nematodes. Although preplant soil fumigation is an effective prevention strategy of soilborne diseases, individual fumigant and technology could not provide effective control of ginger soilborne disease. In our research, different combinations of soil fumigants and seed rhizome treatments were evaluated by monitoring the soil pathogens population, ginger growth, yield, and estimation of economic benefits. RESULTS Soil fumigation effectively reduced the population of soilborne pathogens, and chloropicrin had a better control effect on soilborne pathogens than dazomet did. Preplant soil fumigation and seed rhizome treatment not only provide good control of soilborne disease, but also reduced the incidence of plant foliar pest and disease. Average yield increase rate of seed rhizome treatment was 12.0%; the highest yield increase was 24.4%. The average cost of seed rhizome treatment only increased by about 2.86%, but the rate of net revenue increase for the seed rhizome treatment reached up to 19.1%. CONCLUSION Seed rhizome treatment is a very cost-effective soilborne disease control technology. In the management of soilborne diseases, the combined application of soil fumigation and seed rhizome treatment can reduce the risk of crops infected by soilborne diseases and ensure high and stable crop yields. © 2021 Society of Chemical Industry.

The quantity of soil fumigants has increased globally that has focused attention on their environmental behavior. However, simultaneous analysis of traces of fumigant residues is often unreported because analysis methods are not readily available to measure them at low concentrations. In this study, typical solvent extraction methods were compared with headspace solid-phase microextraction methods. Both methods can be used for simultaneously measuring the concentrations of five commonly used soil fumigants in soil or water. The solvent extraction method showed acceptable recovery (76-103%) and intraday relative standard deviations (0.8-11%) for the five soil fumigants. The headspace solid-phase microextraction method also showed acceptable recovery (72-104%) and precision rates (1.3-17%) for the five soil fumigants. The solvent extraction method was more precise and more suitable for analyzing relatively high fumigant residue levels (0.05-5 μg/g) contained in multiple soil samples. The headspace solid-phase microextraction method, however, had a much lower limits of detection (0.09-2.52 μg/kg or μg/L) than the solvent extraction method (5.8-29.2 μg/kg), making headspace solid-phase microextraction most suitable for trace analysis of these fumigants. The results confirmed that the headspace solid-phase microextraction method was more convenient and sensitive for the determination of fumigants to real soil samples.

The soil phosphorus (P) cycle and P transformation are largely driven by the soil bacterial microbial community. However, little is known about the effects of dazomet (DZ) soil fumigation on soil P and soil microbial communities associated with P transformation. This research investigated P released from three farm soils as a result of DZ fumigation and changes in enzyme activity, gene abundance, and the encoding alkaline phosphatase PhoD microbial community. After DZ fumigation, we observed a briefly significant increase in the available P and the active P fractionation. The soil ALP activity, 16s rRNA abundance, and the phoD gene decreased significantly after DZ fumigation. The abundance and diversity of phoD-harboring microbes also decreased shortly after fumigation, increased significantly 14-28 days later, and then decreased again toward the end of the experimental period of 86 days. The shared OTUs between treatments became fewer with increasing time after fumigation. The changes in available P and the active P fractionation after DZ fumigation were significantly correlated with the abundance of the dominant phoD-harboring microbes. DZ fumigation promoted P mineralization in these farm soils and changed the composition of phoD-harboring microbial communities, which will benefit crops able to absorb and use P.

Biopesticides have proven to be suitable for the control of agricultural diseases and insects. Natural products and micro-organisms have been used as biopesticides worldwide as they can be ...

The highly-damaging root-knot nematode (Meloidogyne spp., RKN) cannot be reliably controlled using only a nematicide such as fosthiazate because of increasing pest resistance. In laboratory and greenhouse trials, we showed that chloropicrin (CP) or dazomet (DZ) synergized the efficacy of fosthiazate against RKN. The combination significantly extended the degradation half-life of fosthiazate by an average of about 1.25 times. CP or DZ with fosthiazate reduced the time for fosthiazate to penetrate the RKN cuticle compared to fosthiazate alone. CP or DZ combined with low or medium rate of fosthiazate increased the total cucumber yield, compared to the use of each product alone. A low-dose fosthiazate with DZ improved total yield more than a low dose fosthiazate with CP. Extending the half-life of fosthiazate and reducing the time for fosthiazate or fumigant to penetrate the RKN cuticle were the two features that gave the fumigant-fosthiazate combination its synergistic advantage over these products used singularly. This synergy provides the opportunity for farmers to use a low dose of fosthiazate which lowers the risk of RKN resistance. Farmers could combine DZ at 30 g m−2 with fosthiazate at a low rate of 0.375 g m−2 to control RKN and adequately control two major soil-borne diseases in cucumber greenhouses.

Despite using fumigants for many decades to control soil-borne pathogens and plant-parasitic nematodes, the influence of soil fumigation on microorganisms involved in the nitrogen-transforming process remains little understood. We used real-time PCR (quantitative polymerase chain reaction) and 16S rRNA gene amplicon sequencing techniques to determine nitrous oxide (N2O) emissions from bacterial microorganisms associated with nitrogen (N) transfer when soils were fumigated with dimethyl disulfide (DMDS) or allyl isothiocyanate (AITC). Our results showed that fumigation with DMDS or AITC increased N2O emissions 6.5–7.3 and 11.2–20.7 times, respectively. The abundance of 16S rRNA and N cycling functional genes initially decreased, but recovered to the unfumigated levels after fumigation. N2O emissions were significantly correlated to the presence of NH4+, NO3−, dissolved amino acids (DAA) and microbial biomass nitrogen (MBN). N2O emissions were not correlated with the abundance of N-transforming functional genes. Metatranscriptomes and dual-label 15N 18O isotope anaylsis revealed DMDS fumigation significantly increased the expression of gene families involved in the N-transforming process, but depressed ammonia oxidation which caused a shift in the N2O pathway from nitrification to denitrification. However, AITC fumigation suppressed most genes involved in the N cycle, but increased the expression of genes that transformed NO2− to NO and further organic decomposition, so that overall there was a shift in the N2O pathway from nitrification to nitrifier denitrification. The information obtained in this study will provide further insights into the N cycling pathways in fumigated soils and into the potential responses of different N-cycling groups after fumigation.

Dimethyl disulfide (DMDS) is an alternative fumigant to methyl bromide that was phased out globally due to its stratospheric ozone-depleting properties. Covering the surface of the soil with a plastic tarpaulin or 'barrier film' when using a soil fumigant is typically used to retain fumigants in the soil and to reduce emissions. Emission levels depend on the film's permeability, which varies mainly according to the film's material, the type of fumigant and the environmental conditions. We used specialized laboratory equipment to test the permeability of four films to DMDS under similar temperature and relative humidity (RH) conditions present in the field: polyethylene (PE), polyvinyl chloride (PVC), polyvinylidene chloride (PVDC) and ethylene vinyl alcohol copolymer (EVOH). This report presents evidence that the influence of temperature and relative humidity on the permeability of four films to the fumigant DMDS: PE，PVC,PVDC, EVOH. This research confirmed that PE and PVC films are relatively permeable to DMDS and PVC was more unstable to a range of environmental condition than other three films; PVDC and EVOH films are relatively impermeable to the fumigant DMDS and the permeability of PVDC was more stable to a range of environmental conditions than EVOH. The cumulative emissions of DMDS from soil covered with PE, PVC, PVDC or EVOH were 21.38%, 27.51%, 1.59% and 1.52%, respectively. As the permeability of PVDC was more stable to a range of environmental conditions than EVOH, PVDC shows potential for use in the field with a volatile fumigant such as DMDS.

The fumigant 1,3-dichloropropene (1,3-D) is widely-used to control pathogenic bacteria, fungi, nematodes and insects in soil before a crop is planted. Although fumigants in general have been reported to have a ‘fertilizer effect’ in the soil by increasing nitrogen availability, little is known of how a specific fumigant such as 1,3-D affects available nitrogen. This study used real-time quantitative PCR (qPCR) and 16S rRNA gene amplicon sequencing techniques to investigate the effects of 1,3-D on microorganisms involved in nitrogen cycling that were present in 2 soils: Jiangxi lateritic red soil and Beijing fluvo-aquic soil. The fumigant 1,3-D temporarily decreased the abundance of 11 functional genes involved in nitrogen-fixing, nitrification and denitrification in both soil types. Different nitrogen cycling groups recovered to the unfumigated level in various incubation phases. Microorganisms containing nifH, nxrB, napA and qnorB genes were most vulnerable to 1,3-D fumigation. However, a stronger and longer inhibition effect of 1,3-D on these 11 functional genes was observed in Jiangxi soil than in Beijing soil. At the same time, the abundance of nifH, AOBamoA, nirS, qnorB and cnorB genes was significantly increased 59 days after 1,3-D fumigation. Fumigation with 1,3-D significantly reduced the nitrogen-fixing bacteria Azospirillum and Paenibacillus; the nitrifiers Nitrosomonas and Nitrospira; and the denitrifiers Pseudomonas, Paracoccus and Sphingomonas. Conversely, fumigation with 1,3-D increased the nitrogen-fixing bacteria Bradyrhizobium and Rhizobium; the nitrification bacteria Nitrosospira and Nitrolancea; and the denitrification bacteria Sphingobium, Alcanivorax, Bacillus, Streptomyces and Aeromonas. Fumigation with 1,3-D therefore caused significant shifts in the species composition and number of microbes directly involved in nitrogen cycling in the short-term. These results contribute toward a better understanding of the impact of 1,3-D fumigation on various types of soil nitrogen-cycling groups.

Anaerobic soil disinfestation (ASD), as a bio-fumigation technology, has been developed to control soil-borne pests. There is increasing evidence showing that carbon sources and cover tarps play an important role in the ASD suppression of soil-borne pests, but little is known about the effect of composted chicken manure (CCM) and totally impermeable films (TIF) against soil-borne pests in the strawberry production system. In experiments, the colonies of Fusarium spp. and Phytophthora spp., which are recognized to cause strawberry soil-borne diseases, decreased significantly after ASD. The soil promoted a significant increase in ammonium nitrogen, nitrate-nitrogen and organic matter, but a decrease in oxidation-reduction potential after ASD. Besides, the strawberry plant height, stem thickness and yield were significantly higher than in the non-amended soil. Compared to the untreated control, ASD, both at 6 and 12 ton/ha of CCM, significantly (p = 0.05) increased strawberry marketable yield and income. The economic benefit could be due to the suppression of soil-borne diseases and the improvement of soil nutrition. The soil bacterial and fungal diversity and richness increased after soil fumigation. The increased presence of biological control agents led to the suppression of soil-borne pathogens. In summary, ASD with CCM amendments could be applied in pre-plant fumigation to control strawberry soil-borne pests, strengthen soil fertility, improve crop yield and increase growers&rsquo, income.

As a substitute for methyl bromide, effects of allyl isothiocyanate (AITC) on nontarget microorganisms in soil are poorly understood. This study measured the half-life of AITC in the soil as well as its effects on the soil substrate-induced respiration (SIR) and on communities of soil bacteria and fungi. The results showed that AITC had a short half-life and a short-term inhibition of SIR; high-throughput sequencing analysis showed that AITC had less effect on bacterial than fungal communities. Fumigation reduced the diversity of soil bacteria temporarily, but stimulated the diversity of soil fungi in the long-term and significantly changed the structure of the fungal community. Following AITC fumigation there were significant increases in the relative abundance of probiotics such as Sphingomonas, Streptomyces, Hypocreales, Acremonium, Aspergillus, and Pseudallescheria that help to control plant diseases. Our study provided useful information for assessing the ecological safety of AITC.

The mechanism of N2O production following chloropicrin (CP) fumigation was investigated in this study. Our results showed that CP fumigation increased N2O production from 23 to 25 times in comparison with the control and significantly decreased the abundance of 16S rRNA and N-cycling functional genes. CP also decreased the soil bacterial diversity and caused a shift in the community composition. The N2O emissions in fumigated soil were significantly correlated with soil environmental factors (NH4+, dissolved amino acid, microbial biomass nitrogen, and NO3-) but were not correlated with the abundance of functional genes. Metatranscriptomes and dual-label 15N-18O isotope analysis revealed that CP fumigation inhibited the expression of gene families involved in N2O production and sink processes and shifted the main pathway of N2O production from nitrification to denitrification. These results provided useful information for environmental safety assessments of CP in China, to improve our understanding of the N-cycling pathways in fumigated soils.

Crofton weed (Eupatorium adenophorum Spreng.) is an invasion in China and its spread speed rate has been faster than anticipated. Laboratory and greenhouse studies were employed to investigate the effect of heavy metal elements on several factors and the survivability mechanism of Crofton weed. Biochemical and ultrastructural methods revealed that this plant tolerated low concentrations of lead (Pb) or cadmium (Cd) individually or in combination as well, based on measurements of photosynthesis, the malondialdehyde and proline content, and the total electrolyte rate. After Pb, Cd or a mixture treatment, the total electrolyte rate, the malondialdehyde and proline content increased in Crofton weed, and leaves became darker than those of the control. Cellular ultrastructure observations showed that a cellular ultrastructure altered, including a thickened cell wall, chloroplast deformation, and damaged mitochondrial membrane. In addition, the activity of catalase, peroxidase and superoxide dismutase and the soluble protein content were affected after treatment with high concentrations of Pb, Cd or a combination. Taken together, these results suggest that Crofton weed has a high tolerance to Pb and Cd at low concentrations but becomes susceptible at high concentrations. These results may help control the environmental threat of Crofton weed or other invasive weed species.

The antifungal activity of oils extracted from Eupatorium adenophorum was tested against five phytopathogens in vitro. Oil extracts inhibited the mycelial growth of Phytophthora capsici which causes phytophthora blight in pepper. The minimum inhibitory concentration of oils against P. capsici was 500μg/ml after 7days incubation. At the ultrastructural level, oil extracts caused complete disorganization of intracellular organelles, cytoplasm depletion, disruption of cytoplasmic membranes and the cell wall. Membrane permeability increased with the increasing concentration of oil extracts. These results suggested that these oil extracts exhibited multiple modes of action including disruption of the cell membrane system. Furthermore, oil extracts combined with synthetic fungicides synergistically inhibited mycelial growth of P. capsici, which creates the possibility of reducing fungicide concentration needed to successfully control phytophthora blight in commercial pepper production. This study's use of multiple methods of analysis has increased our understanding of the mode of action of E. adenophorum oil extracts against P. capsici.

Combined use of chloropicrin (Pic) and 1,3-dicloropropene (1,3-D) is as effective as methyl bromide (MB) at controlling soilborne diseases in many trials and commercial uses. However, Pic and 1,3-D are both highly volatile and may pose strong exposure risks to humans and the environment. A gelatin capsule formulation containing Pic and 1,3-D has been developed to reduce exposure risks to workers and bystanders and improved application safety. We conducted two experiments in tomato and cucumber greenhouses located in Beijing and Qingdao, China, to study the efficacy of Pic plus 1,3-D gelatin capsules applied at different dosages and soil depths. Results indicated that both injection and gelatin capsules of Pic plus 1,3-D provided good control of soil nematodes and reduced disease index of Fusarium wilt and root-knot nematode. Plant yield of tomato and cucumber treated with gelatin capsules was similar to MB treatment. Based on our results, gelatin capsules applied at a soil depth of 15 cm provided better control of soilborne diseases and led to higher fruit yield compared to an application depth of 5 cm. In conclusion, a gelatin capsule of Pic plus 1,3-D is a promising and novel formulation, which not only shows good efficacy in controlling soilborne diseases, but also reduces potential exposure risks of fumigants.

Main-chain nonlinear optical polymers based on novel chromophores with special structures presented good solubility in most of the organic solvents. Polymers PE-1 and PE-2 attained the thermal decomposition temperatures of 305 and 223 °C and glass transition temperatures of 113 and 108 °C, and exhibited only negligible decay in the SHG signal baked at 85 °C over hundreds of hours, respectively. The SHG coefficients of poled films from polymers PE-1 and PE-2 were 26.3 and 35.8 pm/V, respectively. These results indicated that this class of polymers can be used in the preparation of organic electro-optic devices.

BACKGROUND Dimethyl disulphide (DMDS) is a new and effective alternative to methyl bromide for soil fumigation. The effect of biochar on the fate of DMDS in soil is not fully understood. The objective of this study was to determine the degradation kinetics of DMDS in different soils and evaluate the effect of biochar amendment on DMDS degradation using incubation experiments. RESULTS The degradation half-life of DMDS was between 1.05 and 6.66 days under non-sterile conditions, and 12.63 to 22.67 days under sterile conditions in five types of soil. Seven out of the eight tested biochar amendments (BC-2 to BC-8) delayed the degradation of DMDS in soil, increasing the half-life of DMDS in Fangshan soil from 1.05 to 1.16–5.87 days following amendment with 1% (w/w) biochar. The degradation rate of DMDS in Fangshan soil accelerated as the amendment rate of BC-1 increased, and decreased as the amendment rate of BC-7 increased. CONCLUSION Biodegradation is an important degradation route for DMDS in soil, and DMDS degraded faster in alkaline soil. The effects of biochar amendments on DMDS degradation in soil are determined by complex multiple factors (such as surface area, pH and physicochemical composition), rather than by any single property of biochar. © 2017 Society of Chemical Industry