Postharvest UV-C irradiation on cut Freesia hybrida L. inflorescences suppresses petal specking caused by Botrytis cinerea

Postharvest petal specking caused by Botrytis cinerea is a major concern for freesia growers and sellers in Holland and the UK. Germicidal and inducible host defence effects of UV-C irradiation were evaluated. UV-C irradiation of freesia inflorescences after artificial inoculation with B. cinerea (i.e. the germicidal effect) was more effective in reducing petal specking, compared to UV-C treatment before artificial inoculation (i.e. the defence induction effect). Cut freesia inflorescences exposed to 1 kJ m^?2 UV-C after artificial inoculation with 10⁴ B. cinerea conidia mL^?1 displayed reduced disease severity scores, lesion numbers and lesion diameters by 74, 68 and 14%, respectively, compared to non-irradiated control inflorescences. In contrast, UV-C irradiation with 1 kJ m^?2 before artificial inoculation reduced lesion numbers and lesion diameters by 13 and 24%, compared to the non-irradiated controls. Higher UV-C doses of 2.5 or 5 kJ m^?2 reduced disease severity scores, lesion numbers and lesion diameters when applied after artificial inoculation, but enhanced disease when applied before artificial inoculation. Vase life of cut freesia inflorescences irradiated with 0.5, 1 or 2.5 kJ m^?2 UV-C was maintained equal to non-irradiated controls. However, 5 kJ m^?2 resulted in phytotoxicity evident as petal discoloration and reduced vase life compared to non-irradiated inflorescences.     

GC-ITMS determination and degradation of captan during winemaking

Captan and its metabolite tetrahydrophthalimide (THPI) were determined in grapes, must, and wine by GC-ITMS. Pesticides were extracted with acetone/petroleum ether (50:50 v/v). Because of the high selectivity of the ITMS detector, no interferent was found and cleanup was not necessary. Recoveries from fortified grapes, must, and wines ranged between 90 and 113% with a maximum coefficient of variation of 11%. Limits of quantitation were 0.01 mg/kg for both compounds. In model systems, captan and its metabolites, THPI, cis-4-cyclohexene-1,2-dicarboxylic acid, and 1,2,3,6-tetrahydrophthalamic acid, were determined by HPLC. The degradation of captan during winemaking was studied. Captan degraded in must, giving 100% THPI, and at the end of fermentation, only THPI was found in wine. The degradation of captan to THPI was due to the acidity in must and wine. This metabolite was present at low levels on grapes, and, unlike captan, it had no negative effect on the fermentative process. Model systems showed that the mechanism of disappearance of captan in grapes was due to photodegradation and codistillation.     

Sulfate-Zinc interaction on aluminium hydroxide surfaces

Adsorption of Zinc from sulfate or chloride solutions onto aluminium hydroxide was investigated. The interaction between anion and cation was evaluated by simultaneously fitting the adsorption data according to the Bowden model. The strongest Zinc-surface interaction, evidenced by the affinity term (K value), was observed in presence of sulfate. That was interpreted as a result of the enhanced chemical affinity of the surface for the cation due to the adsorption of the anion.     

Effect of sunscreen and antioxidant on the stability of pyrethrin formulations

The stability of pyrethrins in formulations containing different combinations of antioxidant and sunscreen was studied with model system experiments. The mechanism of disappearance of pyrethrins was mainly due to photodegradation, but some loss by codistillation can occur. In formulations, the presence of mineral oil and emulsifiers determined a decrease on codistillation losses. The presence of the antioxidant in formulations even at high concentrations did not affect pyrethrin photodegradation rates, but rising amounts of sunscreen determined a progressive increase on half-life times of pyrethrins. A combination of sunscreen and antioxidant at low concentrations provided an effective protection against sunlight similar to that obtained by high amounts of sunscreen alone.     

Evaluation of a portable glucose meter for use in cattle and sheep

Background: In farm animal practice, determination of blood glucose concentration under field conditions is often necessary. Objective: As there is no portable glucose meter device developed for use in farm animals, the analytical accuracy of a portable glucometer designed for people was evaluated for its use in cattle and sheep. Methods: Blood samples from 90 cattle and 101 sheep were used in the study. Glucose concentration was determined in whole blood immediately after blood collection from the jugular vein with the One Touch Vita portable glucometer and in serum with an enzymatic colorimetric method. The agreement between methods was assessed by Passing and Bablok regression analysis. The precision and the accuracy of the measurements were determined using the concordance correlation coefficient. Results: There was a strong linear relationship between the glucose values obtained using the portable glucometer and those obtained by the bench method in both cattle and sheep. Precision was 95% for cattle and 88% for sheep, whereas accuracy was 92% and 99%, respectively. The mean glucose values obtained using the portable glucometer were significantly lower by 8.3% in cattle and 3.2% in sheep than those determined by the bench method. Conclusion: The One Touch Vita portable glucometer can be used in clinical practice to determine blood glucose concentrations in cattle and sheep, but reference intervals (RI) must be corrected to allow for negative bias. Based on these equations the RI for blood glucose in cattle and sheep using the portable glucometer were corrected to 1.84–4.17 and 2.41–4.35 mmol/L, respectively.     

Molecular diagnostic for detecting the cytochrome b G143S - QoI resistance mutation in Cercospora beticola

The mutation G143S has been associated with high-level strobilurin resistance in laboratory mutant strains of Cercospora beticola, one of the most destructive pathogens in sugar beet plants. By using allele specific primers (PASA-PCR) and agarose gel visualization, a molecular diagnostic was developed for the detection of the G143S resistance mutation. This assay is simple and applicable in low tech laboratory settings, with high reliability when a relatively large proportion of mutated mitochondrial alleles are present in the resistant strains. To achieve detection of resistant alleles at low frequencies, a more sensitive Real Time PCR based assay capable of discriminating resistant (S143) genotypes in frequencies as low as 1:10,000 resistant:sensitive alleles was developed. Both diagnostics were successfully validated in laboratory strains. Subsequently, a large number of C. beticola isolates from QoI-treated sugar beet experimental fields in Greece were screened for resistance to Qo fungicides using these diagnostics and classic bioassays. No proportion of the 143S resistant allele was detected in all field isolates tested, which was in agreement with the phenotypes revealed by the biotests confirming that the efficacy of QoIs against C. beticola has been sustained in Greece 7 years after their introduction.     

Effect of aqueous and lipophilic mullet (Mugil cephalus) Bottarga extracts on the growth and lipid profile of intestinal Caco-2 cells

The importance of n-3 polyunsaturated fatty acid (n-3 PUFA) intake has long been recognized in human nutrition. Although health benefits, n-3 PUFA are subject to rapid and/or extensive oxidation during processing and storage, resulting in potential alteration in nutritional composition and quality of food. Bottarga, a salted and semi-dried mullet ( Mugil cephalus ) ovary product, is proposed as an important source of n-3 PUFA, having high levels of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). In this work, we investigated the extent of lipid oxidation of grated bottarga samples during 7 months of storage at -20 °C and room temperature under light exposure. Cell viability, lipid composition, and lipid peroxidation were measured in intestinal differentiated Caco-2 cell monolayers after 6-48 h of incubation with lipid and hydrophilic extracts obtained from bottarga samples at different storage conditions. The storage of bottarga did not affect the n-3 PUFA level, but differences were observed in hydroperoxide levels in samples from different storage conditions. All tested bottarga extracts did not show a toxic effect on cell viability of differentiated Caco-2 cells. Epithelial cells incubated with bottarga oil had significant changes in fatty acid composition but not in cholesterol levels with an accumulation of EPA, DHA, and 22:5. Cell hydroperoxides were higher in treated cells, in relation to the oxidative status of bottarga oil. Moreover, the bottarga lipid extract showed an in vitro inhibitory effect on the growth of a colon cancer cell line (undifferentiated Caco-2 cells).     

Comparing photosynthetic and photovoltaic efficiencies and recognizing the potential for improvement

Comparing photosynthetic and photovoltaic efficiencies is not a simple issue. Although both processes harvest the energy in sunlight, they operate in distinctly different ways and produce different types of products: biomass or chemical fuels in the case of natural photosynthesis and nonstored electrical current in the case of photovoltaics. In order to find common ground for evaluating energy-conversion efficiency, we compare natural photosynthesis with present technologies for photovoltaic-driven electrolysis of water to produce hydrogen. Photovoltaic-driven electrolysis is the more efficient process when measured on an annual basis, yet short-term yields for photosynthetic conversion under optimal conditions come within a factor of 2 or 3 of the photovoltaic benchmark. We consider opportunities in which the frontiers of synthetic biology might be used to enhance natural photosynthesis for improved solar energy conversion efficiency.     

Genetic variation in cassava for postharvest physiological deterioration

Cassava storage roots start deteriorating 1 to 3 days after harvest due to postharvest physiological deterioration (PPD) which reduces the potential of cassava as a commercial crop. The objective of this study was to examine the extent of genetic variability in cassava for PPD. Genetic variability is important in selecting suitable genotypes for crop improvement. Twelve cassava genotypes were evaluated in a randomized complete block design at three different locations in Uganda for five different harvest times, and PPD assessment was done 7 days after each harvest time. Genotype, location, harvest time, genotype × harvest time and harvest time × location were highly significantly different for PPD. Estimates of phenotypic, genotypic and environmental variance components revealed that a large portion of the phenotypic variance was accounted for by the genotypic component which is an indication of substantial genetic variability among the test genotypes for PPD. This genetic variability is important in a breeding programme because it indicates that significant genetic gain through phenotypic selection is possible for PPD. The results give guidance to breeding efforts for improved shelf life of cassava storage roots.     

Identification of new sources of resistance to Striga gesnerioides in cowpea germplasm

There have been reports of breakdown of striga resistance in previously resistant cowpea cultivars in Burkina Faso. This could be attributed to new striga races emerging or to an increase in the aggressiveness of current striga races. Therefore, cowpea genotypes were evaluated in fields infested with S. gesnerioides at three striga hot spots in Burkina Faso and in pots under artificial infestation with striga races SR 1, SR 5 and SR Kp to identify new, adapted and striga‐resistant sources. Cowpea genotypes showed differential reactions for striga resistance over sites and for striga races in pot experiments, indicating differences in the races involved, and SR Kp was reported as a new race. Resistant sources conferring site‐specific or multiple striga‐race resistance were identified. Genotypes 58‐57, Sanga 2, IT84S‐2049, IT98K‐205‐8, IT93K‐693‐2, KVx771‐10, KVx775‐33‐2, KVx61‐1, Gorom local, Mouride and Melakh conferred resistance to all three striga races. These genotypes are potential donor parents for breeding new, adapted and striga‐resistant genotypes. Cowpea landraces including Moussa local and Niaogo local with farmers' preferred traits were susceptible and need improvement for striga resistance.