Trifolium subterraneum cover cropping for improving the nutritional status of a Mediterranean apricot orchard.

BACKGROUND: The utilization of Trifolium subterraneum L. cover crops may represent an innovative and efficient option in low-input and organic farming, especially in Mediterranean agroecosystems where low and irregular rainfall require frequent soil tillage and use of herbicides to reduce moisture losses and weed competitiveness. Since imbalances of soil macro- and micro-nutrients due to cover cropping establishment could be responsible for numerous problems in specialized orchards, such as disturbances in the normal tree growth and quality of fruits, the objective of this study was to investigate, the cumulative effects of a 3-years established T. subterraneum cover cropping, compared with a spontaneous flora and a conventional management (as a control), on the levels of mineral nutrients in the apricot leaves and fruits. RESULTS: Our findings indicated that T. subterraneum cover cropping tended to stimulate higher leaf macro- and micro-nutrients content than conventional management and flora spontaneous cover cropping. In addition, the presence of T. subterraneum cover cropping, especially with the incorporation of dead mulches into the soil, increased the content of potassium (K), nitrogen (N), calcium (Ca), iron (Fe) and manganese (Mn) in apricot fruits. CONCLUSION: Taking also into account the effects of T. subterraneum cover cropping on both the reduction of soil weed and enhancement of bacteria communities involved in the soil N-cycle, we may suggest its application in Mediterranean orchards as an eco-friendly alternative to synthetic herbicides for weed control and mineral N fertilizers, while enhancing the apricot tree nutritional status and fruit quality. © 2020 Society of Chemical Industry.

Long-Term Effect of Cover Crops on Species Abundance and Diversity of Weed Flora.

Cover crops are gaining in popularity as an eco-friendly tool for weed control in organic and low-input agricultural systems. A 5-year study was carried out in a Mediterranean environment (Sicily, south Italy) to (1) quantify cover crop biomass production and (2) evaluate the effects on weed soil seed bank, aboveground biomass, species richness, species composition and associations between communities. Cover crop treatments included subterranean clover (Trifolium subterraneum L.) and spontaneous flora, both with and without burying dead mulch into the soil, compared to a conventional management treatment. Weed biomass was significantly reduced by subterranean clover, contrariwise to spontaneous flora, with season-dependent results. Cover crop biomass, which ranged from 44 to more than 290 g DW m-2, was negatively correlated to weed biomass. Moreover, subterranean clover decreased the size of the soil seed bank and species richness. Based on relative frequency, a low similarity was found between the conventional management and cover crop treatments. In addition, no significant differences in species composition across treatments were observed, whereas principal component analysis highlighted some associations. The results suggest that subterranean clover cover cropping is a good option for weed management in Mediterranean agroecosystems.

Metabolic and molecular methods to evaluate the organoclay effects on a bacterial community.

The aim of this work was to evaluate the influence exerted by two different commercial organoclays (DELLITE 43B and DELLITE 67G) on a model microbial consortium using microbial metabolic characterization with BIOLOG system and denaturing gradient gel electrophoresis (DGGE) molecular approach. The information obtained from the molecular analyses, in their complex, account for the differences in species composition induced on the reference consortium by the contact with the organoclays under study. DELLITE 43B resulted to produce a marked selective effect, stimulating the quantitative increase especially of Pseudomonas pseudoalcaligenes. A weaker effect was found for DELLITE 67G. On the other hand, Biolog analyses indicated a depressing action exerted by DELLITE 43B on the metabolic activity of the model microbial consortium as a whole. The presence of P. pseudoalcaligenes and B. borstelensis in the bacterial community after the treatments confirmed that a positive change in the microbial structure consortium occurred.

The adsorption and degradation of chlorpyriphos-methyl, pendimethalin and metalaxyl in solid urban waste compost.

To evaluate the feasibility of using compost to prepare substrates for the disposal of pesticide residues, adsorption and degradation studies were carried out on three widely used agricultural pesticides: chlorpyriphos-methyl, pendimethalin and metalaxyl. Obtained from solid urban waste, this compost has been shown to be able to adsorb high levels of chlorpyriphos-methyl and pendimethalin (85%, 100%) whereas metalaxyl was only adsorbed at a level of 37%. However, adding smectite to the compost increased the adsorption of metalaxyl by 117%. Chlorpyriphos-methyl and pendimethalin degraded quickly with half-lives of 1.7 and 14.5 days, respectively, whereas metalaxyl proved more persistent (a half-life of 84 days). Adding ammonium nitrate to the compost accelerated metalaxyl degradation to a half-life of 15 days.

Degradation of poly (lactic acid) and nanocomposites by Bacillus licheniformis.

BACKGROUND, AIM, AND SCOPE: The disposal problem due to non-degradable petroleum-based plastics has raised the demand for biodegradable polymers. The degradation of poly (lactic acid) (PLA) has been studied for several years, but the understanding of involved mechanisms is still incomplete. Based on our previous studies, and it is hypothesized an enzymatic involvement, the aim of this study was to continue investigations on the degradation of PLA and its nanocomposites by Bacillus licheniformis. MATERIALS AND METHODS: Biodegradation of PLA and its nanocomposites (CLOISITE 30B and SOMASIF MEE) was performed on compression-molded, 25 × 25 × 0.6-mm films. Firstly, two plastic films were dipped into sterile nutrient broth inoculated with B. licheniformis and incubated at 32°C. Then, to verify if biodegradation was due to extracellular esterase, the culture broth was filtered to remove B. licheniformis cells, and the plastic materials were put into this broth. RESULTS AND DISCUSSION: PLA degradation by B. licheniformis was accelerated by the presence of organoclays. After 5 months in liquid culture, nanocomposites showed only the 10% of residual mass, compared with the 60% of pure PLA. Extracellular esterase activity was detected in the filtered culture broth confirming that PLA biodegradation was probably due to this enzyme action.

Effects of organoclays on soil eubacterial community assessed by molecular approaches.

The aim of this study was to evaluate the effects of the commercial organoclays, CLOISITE 30B, NANOFIL 804 and DELLITE 26C on soil eubacterial community. An enrichment test was carried out on Nutrient Broth containing the organoclay and the microorganisms previously isolated from soil. Four transfers were made, each after 7 days incubation. The molecular analyses on the eubacterial community were performed before treatment and 7 days after each transfer. DNA was extracted, amplified with eubacterial primers, finally analysed by amplified ribosomal DNA restriction analysis (ARDRA) and denaturing gradient gel electrophoresis (DGGE). The profiles of the samples treated with each organoclay showed the absence, the appearance and an increase in the intensity of some bands. These bands were excised from the gels, and the related microorganisms were identified by DNA sequencing, as Pseudomonas putida, Alcaligenes xylosoxidans, Pseudomonas monteilii and Pseudomonas aeruginosa. NAN804 treatment did not have any influence on soil eubacterial community, CLO30B had a slight toxic effect only on P. putida, instead the DEL26C treatment had a stronger toxic effect on P. putida and a slight toxic effect on P. monteilii. Finally, all the tested organoclays stimulated the growth of both A. xylosoxidans and P. aeruginosa.

Removal of fenhexamid and pyrimethanil from aqueous solutions by clays and organoclays.

The ability of a sodium montmorillonite (CLONa) and two commercial available organoclays having interlayer organic cations possessing different functional groups (CLO20A and CLO30B) was investigated for adsorbing two pesticides namely fenexamid (FEX) and pyrimethanyl (PMT). The two organoclays displayed a higher affinity with the pesticides than the unmodified clay, but the improvement in adsorption capacity varied according to the characteristics of the pesticide and the interlayer organic cation. FEX was adsorbed to a greater extent than PMT by both organoclays, which may be due to the higher hydrophobicity of FEX thereby indicating considerable hydrophobic interaction between the adsorbent/adsorbate systems. Our findings may find application in the removal of water-soluble pesticides from aquifers.

Solubility and adsorption behaviors of chlorpyriphos-methyl in the presence of surfactants.

In the present work changes in the adsorption of the pesticide chlorpyrifos-methyl (CLP-m) on soil colloids induced by application of surfactants were determined using a batch equilibrium method. The surfactants used were sodium dodecyl sulphate (SDS), Tween 20, and dihexadecyldimethylammonium bromide (DHAB). The adsorption isotherms of CLP-m in aqueous medium and in surfactant solutions at concentration equal to the critical micelle concentration (CMC) fitted the Freunlich adsorption equation generally with R(2) values greater than 0.96. While the addition of SDS and DHAB decreased the pesticide adsorption, the addition of Tween 20 increased the pesticide adsorption. The increases or decreases in the adsorption in the experiment revealed that the behavior of CLP-m in soil water-systems mainly depends on the type of surfactant. Moreover water solubility of CLP-m changes by the three surfactants below and above their CMC were studied. While the solubility of CLP-m was enhanced by SDS both below and above the CMC, the solubility of the pesticide was enhanced by DHAB only above the CMC. Tween 20 did not influence the solubility of CLP-m.

Fate and degradation of triasulfuron in soil and water under laboratory conditions.

The behavior and fate of triasulfuron (TRS) in water and soil systems were examined in laboratory studies. The degradation of TRS in both buffer solution and soil was highly pH-sensitive. The rate of degradation could be described with a pseudo first-order kinetic and was much faster at pH 4 than at pH 7 and 9. Aqueous hydrolysis occurred by cleavage of the sulfonylurea bridge to form 2-(2-chloroethoxy) benzenesulfonamide (CBSA) and [(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] (AMMT). AMMT was unstable in aqueous solutions in any pH condition but it degraded more quickly at pH 4 and 9. CBSA did not degrade in aqueous solutions or in enriched cultures but it underwent a quick degradation in the soil. The rates of TRS degradation in sterile and non-sterile soils were similar, suggesting that microorganisms played a minimal role in the breakdown process. This hypothesis is supported by the results of studies on the degradation of TRS by enriched cultures during which the molecule underwent a prevalently chemical degradation.

Use of model soil colloids to evaluate adsorption of phenanthrene and its mobilization by different solutions.

Inorganic (a montmorillonite; a complex of montmorillonite and aluminium hydroxide) and organo-mineral model soil colloids (a complex of montmorillonite, aluminium hydroxide and humic acid) were tested for their capacity to adsorb and desorb phenanthrene. The adsorption-desorption isotherms demonstrated that the inorganic surfaces were able to bind the pollutant, although to a lesser extent than the organo-mineral complex. The capacity of different aqueous solutions to desorb phenanthrene after 1, 7, and 30 days' contact with the model colloids was tested in order to assess their efficacy with respect to the aging effect. The solutions used were 0.01 N CaCl(2), dissolved soil organic matter (DOM), a model root exudates solution (aqueous solution of saccharose, fructose, glucose, fumaric acid, ferrulic acid, and leucine), and three commercial surfactants (sodium dodecyl sulfate, Tween 20, and didecyldimethylammonium bromide). The desorptive capacity of these solutions were compared with that of organic solutions (water-ethanol and n-hexane-ethanol). More than 85% phenanthrene was desorbed after 30 days aging by organic solutions. Among the aqueous solutions, the best results were obtained with dissolved soil organic matter solution and the model root exudates solution which were able to desorb up to 50% phenanthrene after 30 days aging. Such naturally occurring aqueous solutions should be preferred to synthetic compounds to mobilize phenanthrene in contaminated sites without further contaminating the environment.

Behavior of fenhexamid in soil and water.

A study was conducted to investigate fenhexamid (FEX) behavior in soil and in water. FEX proved to be rather stable at acid pH but showed slight degradation at neutral and alkaline pH. After 101 days of FEX spiking of a soil sample, 94% at pH 4, 12% at pH 7 and 23% at pH 9 of the active ingredient was still present. In natural water the rate of FEX disappearance appeared to be slow which may be due to abiotic rather than biotic processes. The soil degradation tests showed low persistence of the active ingredient if a good microflora activity is guaranteed (DT(50) about 1 day). Moreover, in absence of microorganisms, FEX proved to be stable. Humidities of 25 and 50% of Water Holding Capacity (WHC) influenced in equal measure the rate of degradation. From the same soil, a bacterium was isolated and identified as Bacillus megaterium, which was able to metabolize FEX with the hydroxylation of the cyclohexane ring. Moreover, FEX showed an elevated affinity for humic acid (73%), smectite (31%), and ferrihydrite(20%) and low affinity for vermiculite (11%) and kaolinite (7%).

Inexpensive isolation of beta-D-glucopyranosidase from alpha-L-arabinofuranosidase, alpha-L-rhamnopyranosidase, and o-acetylesterase.

Beta-D-Glucopyranosidase (betaG, EC 3.2.1.21) has been isolated from some collateral activities, alpha-L-arabinofuranosidase (Ara, EC 3.2.1.55), alpha-L-rhamnopyranosidase (Rha, EC 3.2.1.40), and o-acetylesterase (Est, EC 3.1.1.53), using a commercial enzyme preparation and a simple method economically sustainable for the food industry. The procedure comprises precipitation of extraneous substances by adding ethanol and CaCl2, ultrafiltration, and adsorption, first on bentonite and then on chitosan. The results obtained were the complete isolation of betaG from the above-mentioned activities, a drastic reduction in extraneous compounds, such as brown substances and polysaccharides, and a slight increase in purification.