Efficacy and environmental fate of copper sulphate applied to Australian rice fields for control of the aquatic snail Isidorella newcombi

Copper sulphate pentahydrate (CuSO₄·5H₂O) is widely used for controlling Isidorella newcombi, an aquatic snail that causes substantial damage to rice crops in southeastern Australia. We conducted field trials on a Birganbigil clay loam soil that demonstrate high levels of efficacy against adult I. newcombi (95% mortality at 6.38 kg ha⁻¹ CuSO₄·5H₂O (1.14 mg Cu L⁻¹)). Dissolved copper fell below the detection limit (0.02 mg Cu L⁻¹) between 7 and 20 d after spraying at application rates up to 2.16 mg Cu L⁻¹ (12 kg ha⁻¹ CuSO₄·5H₂O). Total copper concentrations in the water column fell below the detection limit (0.007 mg Cu L⁻¹) 7–12 d after spraying at initially applied concentrations of 0.52–1.12 mg Cu L⁻¹, but remained detectable (0.01–0.02 mg Cu L⁻¹) until 30 days after spraying (the conclusion of monitoring) when applied at higher initial concentrations (1.18–2.16 mg Cu L⁻¹). There was a strong positive correlation (r² = 0.90, P < 0.001) between copper application rate and copper concentrations in surface sediments 30 d after spraying. Bioassays with immature snails using three different test soils beneath irrigation water showed that underlying soil type strongly influenced the response of snails to applied copper, with significant (P < 0.05) differences between LC₉₀ values which ranged from 0.41 to 1.04 mg applied Cu L⁻¹. Laboratory studies showed that dissolved copper concentrations remained significantly higher (P < 0.05) in the water column above the soil that had the most deleterious effect on copper toxicity. Dissolved organic carbon concentrations were significantly (P < 0.05) higher in both this soil and in the overlying water in the corresponding bioassay system, and correlated more closely with LC₉₀ values than other water chemistry parameters such as total hardness. Our results support the ongoing use of a variable copper application rate of 6–12 kg ha⁻¹ CuSO₄·5H₂O to allow for site-specific variations in efficacy, and suggest that variations in the release of dissolved organic carbon compounds from flooded soils may be a key factor moderating copper toxicity to I. newcombi in rice fields.     

Effects of 1,3-dichloropropene plus chloropicrin on weed seed germination

Telone C-35, a commercial formulation of 1,3-dichloropropene (1,3-D) and chloropicrin (CP), is one of the potential replacements to methyl bromide (MB) for soil fumigation. A laboratory dose–response study and two field trials in tomato were conducted to evaluate their weed control efficacy and their effect on tomato yield. Laboratory studies found that the seeds of Digitaria chinensis were the most sensitive to soil fumigation with Telone C-35, followed by Eleusina indica, Portulaca oleracea and Stellaria media with the LC₅₀ values between 3.35 and 11.68 mg kg⁻¹ soil. Field trials revealed that Telone C-35 applied to the field at 327, 243 and 164 L ha⁻¹ could suppress the percentage of germination weed seeds while maintaining high tomato marketable yields, with no significant differences between MB + CP and the higher two Telone C-35 rates. The yield data from both seasons indicated that all Telone C-35 treatments had a positive effect on tomato yield; there was a 32%–62% increase the mean marketable tomato yield. Our results indicated that Telone C-35 was an excellent MB alternative and could provide acceptable weed control efficacy. Based on our results, Telone C-35, in combination with other alternatives to MB, is recommended to achieve integrated pest management.     

Control of citrus postharvest penicillium molds with sodium ethylparaben

The curative antifungal activity of postharvest sodium ethylparaben (SEP) treatments against citrus green mold (GM) and blue mold (BM) was determined on different citrus species and cultivars artificially inoculated with Penicillium digitatum or Penicillium italicum and incubated at 20 °C and 90% RH for 7 d or stored at 5 °C and 90% RH for 8 weeks plus 7 d of shelf-life at 20 °C. The best concentration was selected in in vivo primary screenings with ‘Valencia’ oranges. SEP at 80 mM was tested at 20, 50 or 62 °C for 30, 60 or 150 s in small-scale trials to determine the best dip treatment conditions. Dips of 80 mM SEP at 20 °C for 60 s were selected and applied alone or in combination with 25 μL L⁻¹ of the conventional fungicide imazalil (SEP + IMZ 25). Imazalil at the very low concentrations of 25 (IMZ 25) or 50 μL L⁻¹ (IMZ 50) was also tested. Effectiveness of SEP alone at 20 °C for 60 s was significantly higher on oranges (cvs. ‘Valencia’ and ‘Lanelate’) than on mandarins (cvs. ‘Clemenules’, ‘Nadorcott’ and ‘Ortanique’), with GM and BM incidence reductions of up to 57–73% after 7 d at 20 °C. SEP was compatible with IMZ 25 and consistently improved its performance, irrespective of citrus cultivars and storage conditions. All treatments were less effective on ‘Clemenules’ mandarins. On ‘Valencia’ oranges stored for 8 weeks at 5 °C and 7 d at 20 °C, the combined treatment was significantly more effective than the single treatments (reductions of GM and BM incidence of about 96–93% and 55–39%, respectively). In additional tests, SEP, IMZ 25 and the combination applied at 20 °C for 60 s prevented GM on ‘Valencia’ oranges treated, inoculated with P. digitatum 24 h later and incubated at 20 °C for 7 d. It can be concluded from these results that SEP might be an integrating nonpollutant control alternative to be included in citrus postharvest disease control programs in the future.     

Effects of nitrogen rate on nitrate–nitrogen accumulation in forage kale and rape crops

Nitrogen fertilizer is applied to supplement soil nitrogen supply to maximize forage brassica crop dry-matter production. However, nitrogen fertilizer applications in excess of that required to maximize growth result in potentially toxic nitrate–nitrogen (NO₃–N) concentrations in grazeable plant tissues. Three experiments, two for forage kale at Lincoln (Canterbury) and one for forage rape at Hastings (Hawke's Bay) in New Zealand were grown under different rates of nitrogen (0–500 kg N ha⁻¹) to determine the effect of different rates of nitrogen on NO₃–N content of different plant parts of the crops. One of the kale experiments was grown with either full irrigation or no rain and no irrigation over summer, hereafter referred to as summer drought. The NO₃–N concentration on a whole plant (weighted average) basis increased from 0·1 mg g⁻¹ dry matter for the control plots to 2·30 mg g⁻¹ for the 500 kg N ha⁻¹ plots for forage kale. It increased from 0·99 for the control plots to 3·37 mg g⁻¹ for the 200 kg N ha⁻¹ plots for forage rape crops. However, NO₃–N concentration increased with N supply under the summer-drought plots from an average of 0·33 mg g⁻¹ when ≤120 kg N ha⁻¹ was applied to 2·30 mg g⁻¹ for the 240 kg N ha⁻¹ treatments but was unaffected by N supply under irrigation. The NO₃–N concentrations were higher in the stems and the petiole (which included the midrib of the leaf) than leaves in all three experiments. The NO₃–N concentration was highest at the bottom of the kale stem and decreased towards the top. We recommend N application rates based on soil tests results, and for conditions similar to the current studies up to 300 kg N ha⁻¹ under irrigation and adjusted lower N rates for regions prone to dry summers.     

Changes in the concentration of avenanthramides in response to salinity stress in CBF3 transgenic oat

Oat avenanthramides have long been known to possess potential nutraceutical and therapeutical properties. The change in avenanthramides 2p, 2c and 2f concentration in four salinity tolerant transgenic oat plants containing CBF₃ gene and non-transgenic control exposed to different levels of salinity stress was investigated. Determination of oat avenanthramides at the nano-scale level was performed using a well-optimized and highly sensitive sequential injection chemiluminescence (SIA-CL) method enhanced by eco-friendly gold nanoparticles biosynthesized from oat biomass extract. Under the conditions of this study, the predominant avenanthramide, which also exhibited the strongest scavenging capacity, was 2c followed by 2p and 2f. At no stress, there was no significant (p ≤ 0.05) difference between the transgenic lines and control regarding the concentrations of the three determined avenanthramides. After exposure to 250 mmol L⁻¹ NaCl, avenanthramide 2c dramatically increased by 170.9%, 580%, 353.6%, 457.6% and 229.1% in the control and the four transgenic lines, respectively. Among the transgenic lines, Agrogle-1 maintained the highest avenanthramides concentration under all salinity levels with maximum values of 71.5 mg kg⁻¹ for 2p, 221.0 mg kg⁻¹ for 2c and 62.0 mg kg⁻¹ for 2f detected at 250 mmol L⁻¹NaCl. The results of this study demonstrated that oat avenanthramides might have a potential role in enhancing abiotic stress tolerance in oats.     

Effect of neemarin on life table indices of Plutella xylostella (L.)

The effects of neemarin at 5, 10, 15 and 20 mg l⁻¹ on the life table indices of Plutella xylostella (L.) were studied on cauliflower in the laboratory. Survivorship was increased with increasing concentrations. A total of 69% eggs hatched at 20 mg l⁻¹ compared 85% in the control. Mortality (d_x) of 1st instars was higher than the other instars in both exposed and unexposed individuals. Life expectancy (e_x) was high in the untreated control and reduced at 20 mg l⁻¹. Development times of immatures were prolonged to 32 days at 20 mg l⁻¹ as compared to 18.6 days in the untreated control. Neemarin significantly reduced the emergence of adults. Potential fecundity (P_f) was 34 females/female/generation at 20 mg l⁻¹ and 92 in the control. The net reproductive rate (R₀) was significantly reduced with the increase in concentration. The intrinsic rate of increase (r_m) and finite rate of increase (λ) were significantly decreased at 20 mg l⁻¹ as compared to other concentrations tested and in the control. Mean generation time (T_c) and corrected generation time (τ) were prolonged at 20 mg l⁻¹ and significantly differed to those of the untreated control. Doubling time (DT) was significantly extended to 28.4 days at 20 mg l⁻¹ as compared to 6.1 days in the control.     

Demographic changes in Helicoverpa armigera after exposure to neemazal (1% EC azadirachtin)

We estimated the effect of 5, 10, 15 and 20 mg l⁻¹ of neemazal (1% EC azadirachtin) on life table parameters of Helicoverpa armigera (Hübner) developing on chickpea (Cicer arietinum L.). The effects were assessed on the survivals emerged from 6th instar larvae that had ingested neemazal-treated chickpea pods. Survivorship (I) and expectancy of life (e_x) were highest with the commencement of age (egg) and decreased gradually with the advancement of age with all the concentrations of neemazal including unexposed cohort. All the eggs hatched in the unexposed group while highest numbers of unhatched eggs (10%) were recorded with 20 mg l⁻¹. Mortality of 1st instars was higher at 20 and 15 mg l⁻¹ than that of other concentration tested. Potential fecundity (pf) was reduced in concentration dependent manner and was lowest with 20 mg l⁻¹ (418 eggs/female/generation) and highest in control (898 eggs/female/generation). Net reproductive rate (R₀) was significantly reduced with the increase in concentration of neemazal. The intrinsic (r_m) and finite rate of increase (λ) were significantly decreased at 20 mg l⁻¹ than that of unexposed population. The mean generation time (T_c) was prolonged at 20 mg l⁻¹ and significantly differed with non-treated individuals. Development of immature stages was prolonged to 38 days with 20 mg l⁻¹ while reduced to 32 days with 15 mg l⁻¹ of neemazal as compared to 37 days in untreated individuals. Doubling time (DT) was significantly extended to 5.02 days with 20 mg l⁻¹ as compared to 3.84 days in the non exposed ones.     

Evaluation of chemical disinfestants in reducing Verticillium dahliae conidia in irrigation water

Irrigation water disinfestation is an unexplored option for reducing Verticillium dahliae inoculum in water and consequently for more efficiently managing Verticillium wilts in Andalusia. We assessed Suppressive Efficacy (SE; water was infested and subsequently treated) and Preventive Efficacy (PE; previously treated water was subsequently inoculated) of OX-VIRIN^®, OX-AGUA AL 25^® and Deccoklor^® in reducing water infestations by V. dahliae conidia. Five concentrations of each disinfestant, the lowest three being recommended by the manufacturer, were tested in vitro against six V. dahliae isolates. Validation assays were carried out in experiments under natural environmental conditions in spring. The four highest concentrations of OX-VIRIN^® (0.8–51.2 mL L⁻¹), the three highest of OX-AGUA AL 25^® (46.4–417.5 μL L⁻¹) and the two highest of Deccoklor^® (0.375 and 3.75 mL L⁻¹), showed an in vitro-efficacy (SE and PE) of 96.2, 80.0 and 100.0% after 30, 5 to 30 and 15 days respectively. Therefore, recommended concentrations for OX-VIRIN^® and OX-AGUA AL 25^® showed a greater in vitro-effectiveness than those recommended for Deccoklor^®. Assays in natural environmental conditions proved that OX-VIRIN^® at the recommended concentration of 3.2-mL L⁻¹, applied every 28 days to water, was the most effective treatment (SE and PE), with a 100% reduction of the average relative viability after 56 days. Other chemical treatments showing high in vitro-efficacy, such as OX-VIRIN^® at 0.8 mL L⁻¹ and OX-AGUA AL 25^® at 46.4 μL L⁻¹ showed an SE of 99.9% after 14 and 28 days when applied every 28 and 14 days, respectively. However, PE of OX-AGUA AL 25^® at 46.4 μL L⁻¹ was only 59 and 38% after 28 and 14 days respectively, depending on the experiment.     

Efficacy of azoxystrobin for the control of cucumber downy mildew (Pseudoperonospora cubensis) and fungicide residue analysis

During a five-year trial (2007–2011), the efficacy of azoxystrobin (Quadris, 250 g a.i. L⁻¹, Syngenta) in two doses (187.5 g a.i. ha⁻¹ and 250 g a.i. ha⁻¹) and chlorothalonil (Bravo 720-SC, 720 g a.i. L⁻¹, Syngenta) at a rate of 1.44 kg a.i. ha⁻¹ was tested for the control of cucumber downy mildew (CDM). Cultivars that were susceptible or resistant to CDM (Regal and Haros, respectively) were tested for their response to fungicide applications. Differences in both disease severity and yield of the cultivars among resistance levels and fungicide treatments were observed. A highly significant and negative correlation was obtained between AUDPC and yield. Higher yields can be achieved by planting more resistant cultivars in combination with lower doses of fungicides. This is an indication that CDM contributes significantly to yield losses in cucumber production in Serbia. While monitoring the degradation of azoxystrobin residues, a decrease in residue levels to 1.0 mg kg⁻¹ below the maximum residue level (MRL) was observed at the end of the pre-harvest interval (PHI).     

Investigation of the high-amylose maize starch gelatinization behaviours in glycerol-water systems

The effect of glycerol on gelatinization behaviours of high-amylose maize starch was evaluated by confocal laser scanning microscopy (CLSM), scanning electronic microscope (SEM), differential scanning calorimetry (DSC), texture analyzer (TPA) and rheometer. Gelatinization of the high-amylose maize starches with glycerol content of 10% (w/w) began at 95.4 °C (T_o), peaked at 110.3 °C (T_p), and completed at 118.9 °C (T_c). The birefringence began to disappear at around 100 °C and finished at 120 °C which corresponded well to the onset and conclusion temperatures obtained by DSC. The high-amylose maize starch granules maintained original morphological structure at 100 °C and swelled to a great degree at 110 °C. The high-amylose maize starch paste formed at 100 °C showed the lowest hardness (39.92 g), while at 120 and 130 °C, showed the highest hardness (610.89 g and 635.43 g, respectively). It should be noted that in going from 100 °C to 110 °C there is a significant increase in the viscosity of the slurry solution. The identical apparent viscosity was observed when the shear rate exceed 100 s⁻¹, resulting from the high-amylose maize starch granules were completely gelatinized at 120 °C, which was consistent with DSC analysis.     

Quinoa (Chenopodium quinoa Willd.) protein hydrolysates with in vitro dipeptidyl peptidase IV (DPP-IV) inhibitory and antioxidant properties

The potential of quinoa to act as a source of dipeptidyl peptidase IV (DPP-IV) inhibitory and antioxidant peptides was studied. A quinoa protein isolate (QPI) with a purity of 40.73 ± 0.90% was prepared. The QPI was hydrolysed at 50 °C for 3 h with two enzyme preparations: papain (P) and a microbial papain-like enzyme (PL) to yield quinoa protein hydrolysates (QPHs). The hydrolysates were evaluated for their DPP-IV inhibitory and oxygen radical absorbance capacity (ORAC) activities. Protein hydrolysis was observed in the QPI control, possibly due to the activity of quinoa endogenous proteinases. The QPI control had significantly higher DPP-IV half maximal inhibitory concentrations (IC₅₀) and lower ORAC values than QPH-P and QPH-PL (P < 0.05). Both QPH-P and QPH-PL had similar DPP-IV IC₅₀ and ORAC values. QPH-P had a DPP-IV IC₅₀ value of 0.88 ± 0.05 mg mL⁻¹ and an ORAC activity of 501.60 ± 77.34 μmol Trolox equivalent (T.E.) g⁻¹. To our understanding, this is the first study demonstrating the in vitro DPP-IV inhibitory properties of quinoa protein hydrolysates. QPHs may have potential as functional ingredients with serum glucose lowering properties.     

Baseline susceptibility of Bemisia tabaci (Genn.) biotype B in southern Florida to cyantraniliprole

Cyantraniliprole 200 mg ai l⁻¹ (Cyazypyr™ 200 SC) is a new xylem systemic insecticide in the anthranilic diamide chemistry class. A systemic laboratory bioassay using cut stems of cotton seedlings was developed to quantify the baseline susceptibility of nymphs and adults of the sweet potato whitefly, Bemisia tabaci (Genn.) biotype B, to cyantraniliprole. Bioassays were conducted on a susceptible laboratory colony and nine field populations collected in 2008, 2009 and 2010 in southern Florida. Bioassays with cyantraniliprole on the susceptible colony (targeting nymphs with exposure initiated at the egg stage) revealed pooled LC₅₀ and slope values of 0.017 mg ai l⁻¹ and 1.766 (SE = 0.125) in 2008, respectively, and 0.013 mg ai l⁻¹ and 1.355 (SE = 0.156) in 2009, correspondingly. Adult bioassays generated pooled LC₅₀ and slope values of 0.049 mg ai l⁻¹ and 3.201 (SE = 0.367) in 2010, respectively. LC₅₀ and slope values targeting nymphs (as above) of field populations ranged from 0.013 to 0.023 mg ai l⁻¹ and 1.425 (SE = 0.167) to 1.923 (SE = 0.187), respectively, in 2008, and 0.023 to 0.034 mg ai l⁻¹ and 1.682 (SE = 0.140) to 2.318 (SE = 0.226), respectively, in 2009. Resistance ratio values at 50% mortality (RR₅₀) on nymphs of field colonies ranged from 0.784 to 1.346 in 2008 and from 1.760 to 2.589 in 2009. Bioassays with adult field populations yielded LC₅₀ and slope values ranging from 0.037 to 0.059 mg ai l⁻¹ and 2.639 (SE = 0.561) to 6.948 (SE = 1.294), respectively, in 2010. The RR₅₀ values for adults from field colonies ranged from 0.752 to 1.207. The overlapping fiducial limits of the LC₅₀ values, the low RR₅₀ values, and the lack of significant differences in the slopes of probit lines between laboratory and field colonies, indicate that the B. tabaci populations present in southern Florida fields were highly sensitive to cyantraniliprole. These data will be helpful in monitoring for any changes in susceptibility as a result of use of the insecticide. The baseline information developed in the present study confirmed the susceptibility of field populations in Florida to cyantraniliprole and will be an essential component of a resistance management program to help ensure the continued viability of cyantraniliprole for B. tabaci management.     

Control of postharvest radish decay using a Cryptococcus albidus yeast coating formulation

An antagonist yeast strain, WY-1, was identified using 18S and internal transcribed spacer (ITS) 1-5.8S-ITS2 rDNA region sequences. The 18S and ITS1-5.8S-ITS2 rDNA sequences of this yeast strain were amplified and sequenced using the universal primer pairs NS1/NS8 and ITS4/ITS5. The ITS1-5.8S-ITS2 rDNA sequence and 18S neighbor-joining tree showed that WY-1 was a strain of Cryptococcus albidus. The biocontrol activity of C. albidus WY-1 on postharvest decay of radishes caused by Alternaria spp. and Fusarium spp. was investigated. In vitro, at 10⁸ CFU ml⁻¹ C. albidus WY-1 inhibited the mycelial weight increases of Alternaria spp. and Fusarium spp. by 45.3% and 59.6%, respectively. In vivo, infection incidence and lesion development of radish decay were suppressed by the application of C. albidus WY-1 at 10⁸ CFU ml⁻¹. After 6 days of incubation at 20 °C or 24 days at 4 °C, disease incidences were 2.8% and 1.4%, respectively; however, the disease incidences of control fruit were 98.6% and 87.5% under these incubation conditions, respectively. Application of C. albidus WY-1 and the chemical fungicide thiabendazole were statistically just as effective. Finally, C. albidus cell counts around inoculation sites remained high at 4 °C even 32 days after inoculation (6.7 × 10⁵ CFU per cm²).     

Effects of Bacillus subtilis strain QST 713 and storage temperatures on post-harvest disease development on greenhouse tomatoes

Tomato plants in two commercial greenhouses were treated with Rhapsody (Bacillus subtilis strain QST 713, rate of 1.45%) once every 4 weeks during 2012–2013 to determine effects on post-harvest fruit infection. Populations of Bacillus and disease incidence were monitored weekly from harvested fruit over an 18-week period. Population levels of Bacillus ranged from 75 to 110 × 10⁴ colony forming units (cfu) cm⁻² of fruit surface area one week after application to 25–30 × 10⁴ cfu cm⁻² of fruit surface area 4 weeks after application. Disease incidence on harvested fruit incubated at 21 °C for 7–10 days was variable, due to variation in inoculum levels within the greenhouse as well as variable environmental conditions. Both disease incidence and severity were significantly reduced on Rhapsody-treated fruit, especially in the 1–2 week period following application. Post-harvest storage temperature (13 °C vs. 21 °C) and incubation time (12 vs. 16 days) had a significant effect on final disease severity. Rhapsody-treated fruit incubated at 13 °C had an average of 1–2% fruit infection compared to up to 20% infection on untreated fruit at 21 °C. The most frequent pathogens affecting fruit quality were Penicillium sp. and Rhizopus stolonifer. Rhapsody applications made every 4 weeks maintained sufficiently high populations of Bacillus on the fruit surface to prevent spread of these fungi onto the fruit, resulting in significant post-harvest disease control on fresh market tomatoes. When combined with storage at 13 °C for no more than 12 days, disease was reduced to negligible levels.     

The control of isariopsis leaf spot and downy mildew in grapevine cv. Isabel with the essential oil of lemon grass and the activity of defensive enzymes in response to the essential oil

The aim of this study was to evaluate the potential of the essential oil of lemon grass (Cymbopogon citratus) for the control of isariopsis leaf spot (Pseudocercospora vitis) and downy mildew (Plasmopara viticola) in grapevine cv. Isabel, the effect of the essential oil on the productivity of the grapevines and the effect of the essential oil on the activity of the enzymes chitinase and catalase. The experiment was conducted in a commercial vineyard over two consecutive crop cycles. Each plant in the experiment was subjected to one of the following nine treatments: 0, 0.5, 1.0, 2.0 or 4.0 mL L⁻¹ essential oil, Tween^® 80%, Bordeaux mixture, Acibenzolar-S-methyl and mancozeb. An analysis of the area under the disease progress curve showed a quadratic response by both diseases to the doses of essential oil during the first and second crop cycles. The essential oil treatments also increased the number and mass of the clusters of fruit as well as the productivity and desirable chemical characteristics of the grape. The activity of chitinase increased as a result of the essential oil treatments, whereas the activity of catalase decreased. The essential oil at doses of 1.0 and 2.0 mL L⁻¹ can serve as an alternative means of controlling isariopsis leaf spot and downy mildew and can also serve to improve the fruit quality of grapes cv. Isabel in tropical regions.     

Minimum gaseous sulphur dioxide concentrations and exposure periods to control Botrytis cinerea

Sulphur dioxide (SO₂) concentrations required to kill the spores and mycelium of Botrytis cinerea and control post-harvest decay of fresh grapes were determined in chamber studies. Effective concentrations and exposure times were simulataneously expressed in a single dosage term, parts per million-hours (p.p.m.-h). This unit is the product of the concentration of SO₂ in parts per million multiplied by the duration of the fumigation in hours. SO₂ dosages that killed 99% of the spores (ED₉₉) were 78.3 ± 22.3 p.p.m.-h at 0°C and 20.3± 2.0 p.p.m.-h at 20°C. These values were determined with continuous concentrations of 25, 50, 100 and 200 p.p.m. SO₂ at high humidity. The mycelium on the surface of infected berries was injured by dosages of 10 p.p.m.-h and was no longer viable after fumigation with dosages of 50–100 p.p.m.-h at 0°C. Infection of inoculated berries at 0°C compared with the controls was 68, 47, 2 and 0% after dosages of 20, 50, 100 and 200 p.p.m.-h, respectively. Reduction in the percentage infection after spore inoculation of berries required a larger dosage ( 100 p.p.m.-h) than that which controlled mycelial growth ( 50 p.p.m.-h). For initial fumigation of grapes after harvest, where control of spores on the surface of grapes is required, 100 p.p.m.-h should be sufficient; for subsequent storage fumigations where control of mycelial growth from latent infections is required, 50 p.p.m.-h should be sufficient. Colorimetric dosimeters have been developed to quantify exposures of humans to SO₂ rapidly and inexpensively for safety purposes. They consist of a sealed glass tube containing a colour-indicating substrate that reacts with SO₂ to produce a coloured product. One end of the tube is opened before use, and the length of the colour change indicates the accumulated dosage in units of p.p.m.-h. They should be placed inside grape packages before fumigation and examined promptly after fumigation. Their accuracy was sufficient for determination of adequacy of SO₂ dosages to control decay.     

Effects of genotype and environment on avenanthramides and antioxidant activity of oats grown in northwestern China

To investigate the effects of genotype and growing environment on avenanthramides and antioxidant activity of oats, the total phenolic content (TPC), avenanthramide compositions, and antioxidant activity were determined for whole oat from 39 cultivars grown in four locations in northwestern China (Inner Mongolia, Qinghai, Shanxi and Gansu). The results demonstrated that environment (E), genotype (G) and the interaction of these factors (E × G) significantly affected TPC, concentration of avenanthramide 2c (2c, ranged from 6.24 to 136.20 mg kg⁻¹), avenanthramide 2p (2p, 6.07–112.25 mg kg⁻¹), avenanthramide 2f (2f, 7.26–222.77 mg kg⁻¹) and antioxidant activity of oats. The effect of E was considerably greater than that of G or E × G. Based on G plus G × E interaction biplots (GGE biplots) analysis, the four locations in northwestern China can be divided into either two or three regions. Qinghai was determined to be distinct from the other locations. Cultivar Bayou 9 and oats grown in Gansu exhibited the highest TPCs, concentrations of 2c, 2p, 2f and antioxidant activity. The results suggest that oats containing more avenanthramides and exhibiting high levels of antioxidant activity could be obtained by selecting an appropriate genotype and growth location.     

Kenaf seed storage duration on germination,emergence, and yield

Kenaf (Hibiscus cannabinus L.) is a potential alternative crop being developed for fiber production. Because planting area varies dramatically from year to year, seed supplies may greatly exceed use so that the excess seed must be stored for one to several years. The objectives of this study were to determine the effect of seed storage duration at 10 °C on germination, vigor, emergence, and yield. Replicated trials were established at Starkville, MS in 1999 and 2000 to evaluate field emergence and biomass yield of kenaf seed from five ‘Everglades 41’ (‘E41’) harvest year seed lots stored at 10 °C in ambient relative humidity for up to 4 years. Germination of these same seed lots under standard (20–30 °C) and cool (20 °C) temperatures, and seed vigor was evaluated over time. Field emergence was the same for the different seed storage durations up to 4 years, but was directly affected by drought conditions for each planted year. Biomass yields ranged from 12.39 to 14.57 Mg ha⁻¹ in 1999 and 16.82 to 18.47 Mg ha⁻¹ in 2000, but were not different between storage durations. Seed germination remained greater than 80% regardless of storage duration. Electrolyte leakage, based on conductivity, was 38–50% less with freshly harvested seed than seed stored for 4 years at 10 °C. However, neither the conductivity nor accelerated aging test were reliable predictors of field emergence. Kenaf seed stored up to 4 years at 10 °C retained germination rates acceptable for commercial use. Neither field emergence nor biomass yield was affected by seed storage duration.     

First report on the presence of Alloxan in bleached flour by LC-MS/MS method

In this work the presence of Alloxan in bread, pastry and cake bleached flour was investigate in order to verify possible risk for consumers related to the use of chemicals for flour bleaching. A selective UHPLC–MS/MS method has been developed and validated for the purpose. Alloxan is one of the possible minor side products of oxidation after chemical bleaching of wheat flours, when several chemical agents are used. One hundred and seventy-five flour samples were analyzed for Alloxan determination. The validation of the method was performed in accordance with the ISO/IEC/EN 17025 for linearity, detection limit, quantification limit, accuracy, precision and ruggedness determination. Satisfactory performances were obtained for the analyte, with a Limit of Detection (LOD) of 0.73 mg kg⁻¹, a Limit of Quantification (LOQ) of 0.85 mg kg⁻¹ and recovery values between 94% and 102%. The present work report for the first time the presence of trace levels of Alloxan in 24% of the analyzed samples, with mean values of 0,95 ± 0,04 mg kg⁻¹. The presence of Alloxan was detected only in cake flour samples. Further studies on toxicological levels of Alloxan are needed in order to evaluate possible risks for consumers linked to the consumption of bakery products.     

Increases in leaf artemisinin concentration in Artemisia annua in response to the application of phosphorus and boron

Malaria resurgence particularly in the third world is considerable and exacerbated by the development of multi-drug resistances to chemicals such as chloroquinone. Drug therapies, as recommended by WHO include the use of antimalarial compounds derived from Artemisia annua L., i.e. artemisinin-based therapies. This work aims to determine how A. annua plant dry matter can be enhanced while maximising artemisinin concentration from understanding the plant's mineral requirements for P and B. Experiments with differing of P, from 5 to 120 mg L⁻¹ and B from 0.1 to 0.9 mg L⁻¹ were undertaken. Mineral nutrients were supplied in irrigation water to potted plants and after a period of growth, dry matter production and leaf artemisinin concentration were determined. Increases in P application enhanced plant growth and total dry matter production. An optimal application rate, with respect to dry matter, was apparent around 30 mg P L⁻¹. Despite increases in P application having no influence on leaf artemisinin concentration, optimal yields of artemisinin, on a per plant basis, were again achieved at supply rate around 30-60 mg L⁻¹. Increasing B application rate had little influence on dry matter production despite increases in B leaf tissue concentration promoting the total amount of B per plant. Leaf artemisinin concentration significantly increased with B application rate up to 0.6 mg B L⁻¹. The higher artemisinin concentrations when multiplied by total leaf dry matter at the higher B application rates produced an increase in total artemisinin production per plant. There was however no further significant effect on leaf artemisinin concentration when B supply concentrations increased further (0.9 mg L⁻¹). Artemisinin production varied between the two experiments to a greater extent than plant dry matter production and the reasons for this are discussed in relation to growing environments and their possible impacts on artemisinin biosynthesis.