Effect of sowing date and rate on the yield and flavonolignan content of the fruits of milk thistle (Silybum marianum L. Gaertn.) grown on light soil in a moderate climate

In the moderate climate of Poland it is recommended that milk thistle (Silybum marianum L. Gaertn.) be grown on fertile soils. The plant, however, develops a strong root system, so a working hypothesis has developed that cultivation can be extended to light soils with periodic water deficits. The aim of the present research was to determine the effects of sowing milk thistle on light soil at different dates and rates on the achene yield and flavonolignan content. This experiment was carried out during 2004-2006 at the Mochelek Experiment Station of the University of Technology and Life Sciences in Bydgoszcz (53°13′ N; 17°51′ E). The average fruit yields were 1.23 t ha⁻¹; those of silymarin were 26.5 kg ha⁻¹. The moisture and thermal conditions during the research years caused the fruit yields to range from 0.55 to 1.68 t ha⁻¹ and silymarin yields from 13.3 to 35.4 kg ha⁻¹. Delaying sowing from early to mid-April increased the plant density and decreased numbers of inflorescences and fruits per inflorescence; as a result, no effect of sowing date on fruit yield was found. Delaying the sowing date increased silymarin content by about 0.4% and its yield by 5.3 kg ha⁻¹. Increasing the sowing rate from 12 to 24 kg ha⁻¹ resulted in a slight (40 kg ha⁻¹) but significant increase in achene yield; however, it did not affect the silymarin content. The average silymarin content in fruits was 2.18%. The ratio of silydianin to silychristin was 1:2.2, and the ratio of silydianin to the sum of silybinin and isosilybinin was 1:3.3.     

QTLs for potato tuber resistance to Dickeya solani are located on chromosomes II and IV

The goal of this research was to identify quantitative trait loci (QTLs) for potato tuber resistance to the soil- and seedborne bacterium Dickeya solani and for tuber starch content, to study the relationship between these traits. A resistant diploid hybrid of potato, DG 00-270, was crossed with a susceptible hybrid, DG 08-305, to generate the F₁ mapping population. Tubers that were wound-inoculated with bacteria were evaluated for disease severity, expressed as the mean weight of rotted tubers, and disease incidence, measured as the proportion of rotten tubers. Diversity array technology (DArTseq) was used for genetic map construction and QTL analysis. The most prominent QTLs for disease severity and incidence were identified in overlapping regions on potato chromosome IV and explained 22.4% and 22.9% of the phenotypic variance, respectively. The second QTL for disease severity was mapped to chromosome II and explained 16.5% of the variance. QTLs for starch content were detected on chromosomes III, V, VI, VII, VIII, IX, XI, and XII in regions different from the QTLs for soft rot resistance. Two strong and reproducible QTLs for resistance to D. solani on potato chromosomes IV and II might be useful for further study of candidate genes and marker development in potato breeding programmes. The relationship between tuber resistance to bacteria and the starch content in potato tubers was not confirmed by QTL mapping, which makes the selection of genotypes highly resistant to soft rot with a desirable starch content feasible.     

Effects of a short period of drought on changes in tuber volume and specific leaf weight. II. Diurnal changes

Summary Single-stemmed potato plants, cv. Bintje, were grown on a nutrient solution under controlled conditions. They were exposed to a short drought stress, or remained untreated. Short-term changes in tuber volume and in specific leaf weight were measured non-destructively. Tubers from control plants increased rapidly in volume during the night and did not grow, or even shrivelled during the day. Tubers of stressed plants did not show a uniform response; some tubers markedly declined in volume during the day. The patterns of volume increase of stressed plants became erratic after the stress, mainly because some plants never fully recovered. Patterns of diurnal fluctuation in tuber volume were similar to diurnal changes in specific leaf weight; tubers within the same stressed plant sometimes reacted differently. In these cases the effects on the diurnal fluctuation partly reflected the long-term effects, reported in an earlier paper.     

Tagging quantitative trait loci for dormancy, tuber shape, regularity of tuber shape, eye depth and flesh colour in diploid potato originated from six Solanum species

Potato breeding aims at breeding diversified cultivars not only suitable for different purposes, but also resistant to diseases, such as late blight caused by Phytophthora infestans , which is a major constraint in potato production. Resistance to P. infestans has been previously introduced into the diploid hybrid population 98-21 from Solanum verrucosum and Solanum microdontum . In the present study, we assessed the segregation of tuber dormancy, tuber shape, regularity of tuber shape, eye depth and flesh colour in this population. Quantitative Trait Loci (QTLs) affecting these important quality traits were tagged using the genetic map developed for this population to locate QTLs for late blight resistance. The most prominent QTL for dormancy was detected on chromosome II and explained 7.1% of the variance. The most important QTLs for tuber eye depth, flesh colour, shape and shape regularity were identified on chromosomes X ( R ² = 14.7%), IV ( R ² = 5.8%), II ( R ² = 8.0%) and III ( R ² = 10.4%) respectively. All traits were also affected by minor QTLs. The obtained results improve our understanding of the inheritance of traits relevant for variety development in potato.     

Biodegradation of new quaternary ammonium compounds in treated wood by mould fungi

The degradation of seven potential wood preservatives based on imidazolium compounds (ICs) and quaternary ammonium compounds (QACs) with a modified anion structure by mould fungi was determined using soil-block method. Experiments were carried out on Scots pine (Pinus sylvestris L.) wood. Two-phase titration and high-performance liquid chromatography (HPLC) method were used to detect and quantify the degradation products. The performed soil-block tests showed that the ICs and QACs with alkoxymethyl substituents were leached from the experimental wood when in contact with moist soil and revealed their fungal detoxification by mould fungi, especially by Gliocladium roseum. The degree of biological decomposition of new compounds was higher than didecyldimethylammonium chloride and didecylmethylpoli(oxyethyl)ammonium propionate. The observations of the colonization by mould fungi were made using the scanning electron microscope (SEM). Decay of treated wood by mould fungi showed its tolerance to QACs.     

Effect of Metal Ions on the Entomopathogenic Nematode Heterorhabditis Bacteriophora Poinar (Nematoda: Heterohabditidae) Under Laboratory Conditions

The effect of sixteen metal ions: Al, Cd, Co(II), Cr(III), Cr(VI), Cu(II), Fe(III), Li, Mg, Mn(II), Mo(VI), Ni(II), Pb(II), Se(IV), V(V), and Zn on the mortality and infectivity ofHeterorhabditis bacteriophora were observed over a 96 hr period. All ions except Pb(II) even at naturally unrealistic concentrations did not cause the mortality of the nematodes. A weak vitalizing effect could eventually be observed with Mn(II), Mg, Fe(III) and Ni(II) (Table 1). However, such treatment generally lowered infectivity of the nematodes with respect to wax moth caterpillars.Galleria mellonella. This effect was particularly significant with Ni(II) and Pb(II).     

Repression of the 14-3-3 gene affects the amino acid and mineral composition of potato tubers

Recently, transgenic potato plants were created showing underexpression of the 20R isoform of the 14-3-3 protein. The transgenic plants grown in tissue culture showed a significant increase in nitrate reductase activity and a decrease in nitrate level. The transgenic line with the lowest 14-3-3 quantity was field-trialed (1997-2000) and analyzed. The reduction in the 14-3-3 protein level consistently resulted in a starch content increase and in an increase in the ratio of soluble sugars to starch in the tubers, although the latter was only barely visible. The determination of amino acid composition in the tubers showed a significant increase in methionine, proline, and arginine content and a slight but consistent increase in hydrophobic amino acid and lysine content in the cells of the transgenic potato plants. We also observed an increase in the crude protein content, from 19 to 22.1% of the control value in consecutive years. It is proposed that all of these changes might have resulted from the downregulation of nitrate reductase and sucrose phosphate synthase activities by 14-3-3, although other potential mechanisms cannot be excluded (e.g., an increase in enzyme protein level). 14-3-3-repressed transgenic plants showed a significant increase in calcium content in their tubers. It is thus proposed that a function of the isolated 14-3-3 isoform is in the control of amino acid synthesis and calcium metabolism. However, the mechanism of this control is as yet unknown.     

Evaluation of PCR markers for <Emphasis Type="Italic">Phytophthora infestans</Emphasis> mating type determination

Late blight is a devastating potato disease caused by Phytophthora infestans. This organism can reproduce asexually and sexually between the strains of two mating types named A1 and A2. Mating type is an important strain characteristic affecting the pathogen’s population structure. We validate different PCR markers for P. infestans mating type determination by comparison of the results obtained with the markers (W16, S1, PHYB) with the pairing test results for 26 isolates collected worldwide and for a group of 146 Polish isolates. This study identifies an interesting feature of the isolates of genotype US-1. For all these A1 mating type isolates, the product specific for A2 isolates is amplified using the marker W16. Analysis of sequences of W16 PCR products indicates high similarity of the US-1 isolates with modern A2 mating type isolates. When US-1 isolates are excluded from analysis, 95 and 96% of isolates are correctly assigned by markers W16 and S1, respectively, when compared with the pairing test results. Marker PHYB produces 14% of discrepant results with the pairing test. Our results show that molecular markers can be useful tools for P. infestans mating type determination, but their application should be preceded by validation in each local population since their efficiency may vary depending on a pathogen’s genotype.