Genetic Structure of Peruvian Populations of Phytophthora infestans

ABSTRACT Isolates of the late blight pathogen Phytophthora infestans (n = 327) from the central to southern Peruvian Andes were systematically collected in 1997 to 1999 and analyzed to determine the pathogen's population structure at its host's center of diversity. No isolates of the A2 mating type were detected. Cluster analysis of DNA fingerprinting data indicated that the collection consisted of five major groups that were interpreted to be clonal lineages. Two of the lineages (US-1 and EC-1) have been previously described, and three (PE-3, 5, and 6) are described here for the first time. Collections from three areas in the central Peruvian Andes, including two key sites used in an international potato breeding program, consisted of isolates of the EC-1 lineage, which has been reported to dominate the pathogen population in Andean countries to the north of Peru. The collections from Cusco and Puno were more diverse. More than one lineage was detected in 10 of the 20 fields sampled in Cusco. Data on virulence, metalaxyl sensitivity, and band data for allozymes, mitochondrial DNA, and ipiB1 suggested that PE-3 may have been produced through recombination events between US-1 and EC-1. Restriction fragment length polymorphism and amplified fragment length polymorphism marker data were not consistent with this hypothesis.     

Nitrogenous humic fertilizers by ammoniation of humic material obtained from kraft black liquors

Humic materials obtained from kraft black liquor were ammoniated with aqueous ammonia in a stainless-steel batch reactor. The effects of different variables, viz. total acidity of the humic material, reaction temperature and ammonia concentration, on the extent of N fixation by the humic material is reported. A 2³ factorial design was used for the experiments. Results show that products containing up to 11.8 wt% total N can be obtained. The optimum operating conditions in order to obtain a high nitrogen content are: acidity 60 mL NaOH g^?1 of sample; temperature 100 °C; and aqueous ammonia concentration 8 wt%.     

Ultrafiltration of a Waste Emulsified Cutting Oil using Organic Membranes

The influence of operating conditions on permeate flux was investigated using organic ultrafiltration membranes to treat a synthetic cutting-oil emulsion containing 0.05 to 0.8 wt. % oil. A commercial cutting oil, Alba-Kool, and four organic ultrafiltration membranes, two made of polysulfone (PM10 and PM30) and the other two of regenerated cellulose (YM10 andYM30), with cut-off sizes of 10 000 or 30 000 Dalton, were used.All experiments were performed in a commercially available stirred ultrafiltration cell. Within the range of operating conditions studied, it was found that the highest fluxes wereobtained at the following conditions: crossflow velocity (rotation speed) of 375 rpm, temperature of 40 °C andtransmembrane pressure of 0.1–0.15 MPa. Oil rejections between99 and 99.9% were obtained. Complete membrane regeneration wasachieved with a 2 vol. % aqueous solution of a commercial cleaning agent (Derquim+, Panreac).     

Characterization of the resistance to <Emphasis Type="Italic">Phytophthora infestans</Emphasis> in local potato cultivars in Bolivia

This experiment was carried out to investigate whether and how much field resistance to late blight, caused by Phytophthora infestans, is present in the local cultivated potato germplasm. In total 36 entries were compared in a field experiment in an area highly conducive to late blight development. Of the 36 cultivars 32 were local cultivars belonging to five Solanum species, S. tuberosum (1 accession), S. andigena (18), S. juzepczukii (2), S. stenotomum (9) and S. ajanhuiri (2). The other four cultivars were derived from breeding programmes, one being the Dutch cultivar Alpha used as a highly susceptible control. The 36 cultivars were planted according to a simple 6 × 6 lattice design with three replicates. Each replicate was divided in six incomplete blocks each with six cultivars. The disease severity was assessed weekly during 9 weeks starting 48 days after planting. The area under the disease progress curve (AUDPC) was used as a measure of the field resistance. Nine isolates from surrounding potato fields were tested for their virulence to the resistance genes R1–R11 using 22 differential cultivars. The components of the field resistance of 19 of these cultivars were compared in the greenhouse using a local isolate with virulence to all known R-genes, except to R9. The nine isolates represented seven races with a race complexity varying from 7 to 10 virulence factors. All isolates carried virulence against R1, R2, R3, R7, R10 and R11, while virulence against R9 was absent. The AUDPC among the 32 local cultivars ranged from very large, significantly larger than that of ‘Alpha’ to very small. The AUDPC from S. stenotomum accessions ranged from very large to intermediate, those from S. andigena accessions from large to very small. Especially among the S. andigena accessions interesting levels of field resistance were found. Four components of field resistance were assessed, latency period (LP), lesion size (LS), lesion growth rate (LGR) and relative sporulation area (RSA). All four showed a considerable variation among the cultivars. The LP ranged from 3½ to 6 days. The LS ranged from 225 mm² to 20 mm². The LGR varied about six-fold, the RSA more than 10-fold. The components tended to vary in association with one another. LP and LGR were well associated with each other and had a significant correlation with the AUDPC.