Polymerisation of added coniferyl alcohol by inherent xylem peroxidases and its effect on fungal decay resistance of Norway spruce

It is known that active peroxidase isozymes exist in mature wood of Norway spruce (Picea abies L. Karst.) and that they remain active for years and are found even in the heartwood (in Scots pine), where all cellular activity has ceased. This peroxidase activity was utilised in the impregnation of wood blocks with a natural monolignol, coniferyl alcohol and hydrogen peroxide. The hypothesis was that the internal wood peroxidases would oxidise the added monolignol and bind it stably into the cell wall matrix, which could hinder fungal decay. Since coniferyl alcohol is not very soluble in water, the impregnation was done under vacuum with an acetone–water solution containing 10% coniferyl alcohol and 0.4 mM H₂O₂ at room temperature (ca. 0.02 g of coniferyl alcohol was added to 1 g of wood). After impregnation, dimers of coniferyl alcohol and free coniferyl alcohol were found in acetone extracts with GC–MS analysis. Penetration of coniferyl alcohol and non-extractable reaction products were studied from the wood blocks with FTIR PAS technique. The wood samples treated were also subjected to a fungal decay test with Coriolus versicolor. This treatment hindered fungal decay in a 60-day experiment and led to a dry weight loss of 8.8% in comparison with 19.9% in the control. The reactions of coniferyl alcohol and H₂O₂ in the presence of peroxidases are discussed as well as the use of monolignols to increase wood decay resistance.     

Geographical patterns of phenotypic diversity in <Emphasis Type="Italic">Oryza sativa</Emphasis> landraces of Côte d’Ivoire

The knowledge of agro-morphological diversity and the distribution pattern of variation among conserved accessions could be an invaluable aid in germplasm management and crop improvement strategies. In this study, the geographical pattern of morphological variation of 880 landrace rice (Oryza sativa (L.)) accessions in Côte d’Ivoire was evaluated for 13 agro-morphological characters. Shannon –weaver diversity index indicated an overall mean of 0.47 ± 0.07 in the collection, with the greatest diversity from derived Savanna and north-west (H′ = 0.52 and 0.50) while the west-central had the lowest diversity (H′ = 0.41). Canonical discriminant analysis showed that traits such as panicle length, grain size (weight and length), tillering ability, number of days to heading and maturity were the main discriminatory characteristics. Result of the phenotypic frequency shows that, the landraces from the north and north-western zones were mostly tall, early heading and maturity, compared to those from the west and west-central which were mainly dwarf to medium height, late heading and maturing. This differential distribution of landraces with height, heading and maturity period reflected the distribution pattern of different Oryza sativa landraces in Côte d’Ivoire, which could be useful in germplasm management and breeding programs.     

Antibacterial activity and phytochemical study of six medicinal plants used in Benin

The ethanol extracts obtained from Psidium guajava, Flacourtia flavescens Boswellia dalzielii, Ficus exasperata, Pavetta corymbosa and Hybanthus enneaspermus, six species traditionally used in Benin to treat several infectious diseases, were evaluated for their in vitro antimicrobial activity against Staphylococcus aureus, Enteroccocus feacalis, Escherichia coli and Pseudomonas aeruginosa. The minimum inhibitory concentration of extracts was determinate using the microplate dilution method. The presence of major phytoconstituents was detected qualitatively. The diphenylpicrylhydrazine radical scavenging activity was also performed. The extracts exhibited antibacterial activities against the tested bacteria. Boswellia dalzielii, Psidium guayava, Pavetta corymbosa and Flacourtia flavescens exibited the lowest minimum inhibitory concentration values (0.313-2.5 mg mL(-1)). Pseudomonas aeruginosa was the lest sensitive microorganism with MIC values higher than 10 mg mL(-1). In antioxidant assay the crude extracts of B. dalzielii and P. corymbosa appeared to be as potent as quercetol with an inhibition percentage of 83 and 75.3% at 10 microg mL(-1) which is comparable to 75.9% for quercetol at the same concentration.     

Fast track participatory approach to release of elite cassava genotypes for various uses in Nigeria’s cassava economy

The aim of the Integrated Cassava Project (ICP) of the International Institute of Tropical Agriculture was to pre-emptively manage the cassava mosaic disease (CMD) to avert an imminent and increasing possible threat of the Ugandan strain of the CMD virus of the pathogen from doing damage to the Nigerian cassava economy. The strategy was to engage in activities that would lead to cultivar-substitution by replacing the susceptible varieties on farmers’ fields with superior genotypes that are not only CMD resistant or tolerant but also high yielding with good dry matter content. A fast track participatory selection approach was used in 2 years to release nine new lines in Nigeria. It was intensive and several lessons were learnt. The varieties released after 2 years were TMS 98/0510, TMS 98/0581, TMS 97/2205, TMS 98/0505, TME 419, TMS 92/0326, TMS 96/1632, TMS 98/0002, and TMS 92/0057.     

Measurements of oxygen consumption and ammonia excretion of Atlantic salmon (Salmo salar L.) in commercial-scale, single-pass freshwater and seawater landbased culture systems

The oxygen consumption of Atlantic salmon was measured in large culture tanks for a period of 20 months from the parr to the adult stage. In addition, diurnal sampling was conducted for estimation of both oxygen consumption and ammonia excretion. The oxygen consumption was affected especially by temperature, season and smoltification. For parr the oxygen consumption rate was 1–6 mg O₂/kg min and the ammonia excretion rate was 0·037–0·13 mg N/kg min from autumn to spring. The corresponding rates for adult salmon during the period October to July were 1·5–4·5 mg O₂/kg min and 0·075–0·13 mg N/kg min.