Biological control of botrytis bunch rot in organic wine grapes with the yeast antagonist Candida sake CPA‐1

The aim of this research was to confirm the efficacy of the yeast antagonist Candida sake CPA‐1 in suppressing botrytis bunch rot development, in an organic vineyard under Mediterranean conditions for two seasons, and compare its performance with that of two biologically based products currently registered for botrytis bunch rot control in New Zealand. In 2009, treatments applied were: commercial formulations of Ulocladium oudemansii (BOTRY‐Zen^®) and chitosan (ARMOUR‐Zen^®), C. sake CPA‐1 combined with the fatty acid‐based additive Fungicover^® and combinations of these products. All treatments were applied six times between early flowering and harvest and compared with an unsprayed control. In 2010, the treatments focused on C. sake and Fungicover and the number of applications was reduced from six to four. The population dynamics of U. oudemansii and C. sake were measured and wine quality tests were carried out in both seasons. Disease control achieved by C. sake treatments in 2009 were comparable to those achieved by BOTRY‐Zen and ARMOUR‐Zen. Applications of C. sake plus Fungicover between flowering and harvest significantly (P < 0·05) reduced botrytis bunch rot incidence and severity by 64% and 90%, respectively, compared with the untreated control in 2009, and by 67% and 89%, respectively, in 2010. Treatments did not adversely affect wine quality parameters after treated grapes were processed. Candida sake consistently provided effective control of botrytis bunch rot in grapes under different meteorological and disease pressure conditions, thereby improving its potential for future commercial applications.     

Biochemical responses to ultraviolet‐C radiation and methyl jasmonate in Pinus radiata seedlings that accompany induced resistance to Diplodia pinea

Irradiation of Pinus radiata seedlings with ultraviolet‐C (UV‐C) radiation or spray application of methyl jasmonate (MeJA) each resulted in induced resistance to subsequent wound inoculation with Diplodia pinea. Induced resistance was expressed by lower incidence of disease and by reduced size of stem lesions than in untreated seedlings. UV‐C was more effective than MeJA and the induced resistance was greatest in seedlings that were irradiated with UV‐C for 60 min, 1 week before pathogen inoculation. Induced resistance in the UV‐C treated stems was concomitant with increases in peroxidase (POX) and polyphenol oxidase (PPO) activity but showed no correlation with concentrations of α‐pinene and β‐pinene or total phenolics. Furthermore, POX induction in stem tissue was cumulative and was greatest after three repeat treatments with UV‐C at 6, 3 and 1 week before inoculation. In contrast to UV‐C, MeJA induced a significant increase in β‐pinene concentration in stem tissue but did not affect PPO activity. POX activity was induced by MeJA in stems, although to a lesser extent than by UV‐C, but was not affected in needles. This appears to be the first report demonstrating the use of UV‐C radiation to induce resistance to fungal infection in a coniferous species. The implications of the underlying differences between UV‐C‐ and MeJA‐mediated resistance to D. pinea are discussed.     

Identification and expression pattern of a glutathione S‐transferase in Echinochloa crus‐galli

Plant glutathione S‐transferase (GST) forms a major part of the herbicide detoxification enzyme network in plants. A GST cDNA was isolated from Echinochloa crus‐galli and characterised. The gene, designated EcGST1 (E. crus‐galli GeneBank no: JX518596 ), has a 684 bp open reading frame predicted to encode a 25 kD protein. Sequence alignment showed that EcGST1 is a GST homologue. Its expression in response to quinclorac treatment was monitored in seedlings (leaves and roots) and adult plants (leaves, roots, stems and seeds) of quinclorac‐resistant (R) and susceptible (S) biotypes of E. crus‐galli. EcGST1 expression was 1.5–3 times greater in the R plants than in the S plants. However, after exposure to quinclorac, the difference in the expression levels of EcGST1 in R plants, compared with S plants, increased to a ratio of 6–10. Enhanced EcGST1 levels should enable greater quinclorac detoxification following quinclorac stimulation in R plants. GST‐based metabolism may be partially responsible for resistance to quinclorac in E. crus‐galli. The results suggest a new resistance mechanism for this R biotype in Chinese rice fields.     

Influence of variety on the within-plant distribution of cassava green spider mite (Acari: Tetranychidae), and leaf anatomical characteristics and chemical components in relation to varietal resistance

The within-plant distribution of the cassava green spider mite, Mononychellus tanajoa Bondar, and the anatomical characteristics and the chemical components relating to varietal resistance of cassava, were studied using 11 cassava genotypes with varying levels of resistance for two dry seasons and one wet season. The results show that M. tanajoa aggregates on the top leaves of cassava at low levels of resistance as compared with a more even within-plant distribution at higher levels of resistance. Thus, for accurate sampling of mite populations, it might be important to consider young and old leaves, not just the young leaves, in fields containing resistant and susceptible cassava genotypes. Correlations between the anatomical characteristics and mite population density and damage scores were not consistent across months, either within or over seasons. This suggests that leaf anatomical characteristics may not be important in the varietal resistance of cassava to M. tanajoa. During the dry season, mite population density was positively correlated with leaf nitrogen, potassium and phosphorus and negatively correlated with leaf calcium and fat. Only calcium was negatively associated with mite damage at the peak of the dry season (January 1993 and 1994). Breeding cassava genotypes with high levels of leaf calcium and fat, and low levels of leaf nitrogen, potassium and phosphorus, may improve the level of resistance to M. tanajoa.     

Conservation tillage systems for sorghum production under semi‐arid conditions in India

Abstract

Field research was conducted near Hyderabad, India, during 1981 and 1982 to investigate zero‐tillage and reduced‐tillage systems for production of sorghum (Sorghum bicolor (L.) Moench.) under semi‐arid tropical conditions. Part of the investigation compared post‐seeding hand weeding and herbicide treatments for weed control efficacy. The results showed that shallow pre‐seeding tillage was just as effective as deep cultivations in producing high sorghum fodder and grain yields provided weeds were controlled after crop emergence. Both tillage regimes were more effective than a no tillage regime which received only a mixture of glyphosate and 2,4‐D prior to seeding. Post‐seeding weed control practices were essential to maintain high fodder and grain yields of sorghum. Hand weeding and inter‐row blade harrowing were more effective than atrazine applied pre‐emergence or 2,4‐D applied post‐emergence.     

Comparative biology of Mallada desjardinsi (navas) and Chrysoperla congrua (walker) (Neuroptera: Chrysopidae), predators of Helicoverpa armigera (Hubner) (Lepidoptera: Noctuidae) and aphis gossypii (glover) (Homoptera: Aphididae) on cotton in eastern Tanzania

The developmental biology of Mallada desjardinsi (Navas) and Chrysoperla congrua (Walker) on the American bollworm, Helicoverpa armigera and the cotton aphid, Aphis gossypii was studied in the laboratory at 28–32°C. Total larva! periods of M. desjardinsi and C. congrua on H. armigera eggs were 14.4 and 14.8 days respectively. However, when reared on A. gossypii larval periods of M. desjardinsi and C. congrua were 14.9 and 13.5 days respectively. When reared on H. armigera 52.9% and 25% respectively of third instars of M. desjardinsis and C. congrua sp. died before pupation. However, when reared on A. gossypii 82.6% and 46.9% respectively of third instars of M. desjardinsi and C. congrua died before pupation. Thus, H. armigera eggs and A. gossypii nymphs were both adequate but not optimal diets for chrysopid larval development. The number of prey consumed by M. desjardinsi and C. congrua increased with instar. Total larval consumption of H. armigera by M. desjardinsi and C. congrua was determined to be 135.5 and 169.8 eggs respectively. However, total larval consumption of A. gossypii by M. desjardinsi and C. congrua was found to be 189.0 and 171.8 nymphs respectively. Because of its longer larval period, and higher consumption of A. gossypii, M. desjardinsi would be better suited for use against A. gossypii than C. congrua. In contrast, C. congrua whose consumption of H. armigera was higher than that of M. desjardinsi although their larval periods were similar, would appear promising for control of H. armigera.     

Low root‐to‐root transmission of a tobamovirus,yellow tailflower mild mottle virus,and resilience of its virions

Tobamoviruses are serious pathogens because they have extremely stable virions, they are transmitted by contact, and they often induce severe disease in crops. Knowledge of the routes of transmission and resilience of tobamovirus virions is essential in understanding the epidemiology of this group of viruses. Here, an isolate of the tobamovirus yellow tailflower mild mottle virus (YTMMV) was used to examine root‐to‐root transmission in soil and in a hydroponic growth environment. Root‐to‐root transmission occurred rarely, and when it occurred plants did not exhibit systemic movement of the virus from the roots to the shoots over a 30‐day period. The resilience of YTMMV virions was tested in dried leaf tissue over time periods from one hour to one year under temperatures ranging from ?80 to 160 °C. Infectivity was maintained for at least a year when incubated at ?80 or 22 °C, or at fluctuating ambient temperatures of 0.8 to 44.4 °C, but incubation under dry conditions at 160 °C for >4 days eliminated infectivity. Exposure of virions to 0.1 m sodium hydroxide or 20% w/v skimmed milk solution for 30 min, treatments recommended for tobamovirus inactivation, did not abolish infectivity of YTMMV.     

Accumulation of sorghum phytoalexins induced by Colletotrichum graminicola at the infection site

Microspectrophotometry was performed on intact, pigmented vesicle-like inclusions within living sorghum cells that were accumulating phytoalexins as a response to attempted fungal infection. The results indicate that the deoxyanthocyanidin phytoalexins are present in inclusions. Moreover, the phytoalexin concentration within a single inclusion, based on luteolinidin, was calculated to be 0·15 m. The amounts of luteolinidin and apigeninidin in cells involved in the phytoalexin response at individual infection sites were also determined. The data showed that luteolinidin accumulated to levels of 0·48–1·20 ng/cell whereas apigeninidin accumulated to levels of 0·24–0·91 ng/cell. The results of both analyses confirmed that at the infection site the deoxyanthocyanidins accumulate to levels in substantial excess of those required for inhibition of the fungus Colletotrichum graminicola.