The effect of selenium (Se) treatments on potato growth and Se, soluble sugar, and starch accumulation was investigated. Potato plants were cultivated in quartz sand without or with sodium selenate (0, 0.075, 0.3 mg Se kg(-1) sand). In young potato plants, Se treatment resulted in higher starch concentrations in upper leaves. The tuber yield of Se-treated potato plants was higher and composed of relatively few but large tubers. At harvest, the starch concentration in tubers did not differ significantly between treatments. The higher Se addition (0.3 mg Se kg(-1)) may have delayed the aging of stolons and roots, which was observed as high concentrations of soluble sugar and starch. Together with the earlier results showing elevated starch concentration in Se-treated lettuce, the findings of this research justify the conclusion that Se has positive effects also on potato carbohydrate accumulation and possibly on yield formation.

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Effects of Se fertilization on potato processing quality, possible changes in Se concentration and form in tubers during storage, and retransfer of Se from seed tubers were examined. Potato plants were grown at five selenate (SeO4(2-)) concentrations. Tubers were harvested 16 weeks after planting and were stored at 3-4 degrees C prior to analysis. The results showed that the Se concentration did not decrease during storage for 1-12 months. In tubers, 49-65% of total Se was allocated in protein fraction, which is less than found in plant leaves in a previous study. The next-generation tubers produced by the Se-enriched seed tubers had increased Se concentrations, which evidenced the relocation of Se from the seed tubers. At low levels, Se improved the processing quality of potato tubers by diminishing and retarding their raw darkening. The value of Se-enriched potato tubers as a Se source in the human diet was discussed.

Selenate fertilization is an effective way to secure selenium (Se) nutrition in Se-poor areas but the cycling of the added selenate in the soil-plant system requires further clarification. We examined the Se uptake efficiency of wheat and ryegrass and Se distribution within these plants in two pot experiments. The behaviour of added selenate in a sand soil under wheat was monitored by sequential extractions during a ten-week growing period. In addition, the relationship between Se uptake of ryegrass and the salt extractable and ligand exchangeable Se in a sand and silty clay soil were studied. The added selenate remained mainly salt soluble in the soil throughout the monitoring. Se uptake by wheat comprised 12% of the soluble Se pool in soil and extended over the whole period of growth. In wheat, over 50% of Se accumulated in grains. The Se uptake of ryegrass comprised, on average, 40% of the soil salt soluble Se. In ryegrass, over 80% of the Se accumulated in roots. The distribution pattern of Se in plants can clearly have a major influence on both the Se cycle in soil and the nutritional efficiency of Se fertilization. The simple salt extraction showed fertilizationinduced changes in the soluble soil Se pool, whereas the ligand exchangeable Se fraction reflected the difference in the nonlabile Se status between the two soils.

SUMMARYCultivation of winter turnip rape (Brassica rapa L. ssp. oleifera (DC.) Metzg.) in Finland has been limited because of its reputation as an unreliable crop and its mid-season sowing time of July, when fields are already sown to other crops. An alternative management practice for winter turnip rape is proposed whereby it would be sown as a mixed crop simultaneously with spring cereals. The growth and yield formation of winter turnip rape grown in mixed stands with four different spring cereals was studied in two field experiments conducted in 2009–11. Pure and mixed stands of winter turnip rape and spring cereals were established in May at two different cereal and winter turnip rape stand densities. Subsequent to cereal harvest, one-third of each winter turnip rape plot was harvested for biomass in autumn, before cessation of growth. Three plant stand types, May- and July-sown monocrops and a mixed crop with oat (Avena sativa L.) were sampled for forage analysis. Plant stand densities were monitored from establishment until maturity. Winter turnip rape yield and its quality, including oil content, protein content and thousand seed weight, were determined. Following favourable overwintering conditions, winter turnip rape established with cereals yielded comparably to that of pure stands in terms of both quantity and quality. However, a pure stand of winter turnip rape out-yielded mixed crop stands after unfavourable overwintering conditions. Leaf removal decreased plant survival and seed yield. Establishing winter turnip rape with a cereal in May is an alternative to sowing it as a monocrop in July. A higher seeding rate is needed for under-sown winter turnip rape. Furthermore, autumn-harvested winter turnip rape monocrop forage potentially represents a high-protein supplement for ruminants.

Potatoes (Solanum tuberosum L.) supplemented with increasing amounts of sodium selenate were analyzed for glycoalkaloid (GA) content. GAs were extracted with 5% acetic acid from freeze-dried tubers of two potato cultivars, Satu and Sini, harvested 10 weeks after planting as immature. The GAs alpha-solanine and alpha-chaconine were quantified by reverse-phase high-performance liquid chromatography (RP-HPLC) with diode array detection. Two independent experiments were performed. In the first experiment, the total GA concentration +/- standard error of the tubers ranged between 105 +/- 9 and 124 +/- 10 mg kg(-1) fresh weight in Satu and between 194 +/- 26 and 228 +/- 10 mg kg(-1) fresh weight in Sini. The ratio of alpha-solanine to alpha-chaconine was 0.2 in Satu and 0.5-0.6 in Sini. In the second experiment, the total GA concentration +/- standard error was 75 +/- 4 to 96 +/- 11 mg kg(-1) fresh weight, and the ratio of alpha-solanine to alpha-chaconine was 0.3-0.4 in Satu. A high sodium selenate supplementation (0.9 mg of Se kg(-1) quartz sand) slightly decreased the GA content in Satu, but this decrease was not statistically significant. Furthermore, at this addition level the Se concentration increased to a very high level of 20 microg g(-1) dry weight, which cannot be recommended for human consumption. In both experiments, the Se concentration in tubers increased with increasing sodium selenate application levels. Our results show that acceptable application levels of selenate did not have an effect on the GA concentration in immature potato tubers.

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The aim of this study was to investigate the effect of Se enrichment on the growth of sprouts and growth vigour of seed potatoes (Solanum tuberosum L.) stored for 2 to 8 months. Our results showed that Se did not affect the duration of dormancy. At the high addition levels (0.075 and 0.9 mg kg -1 quartz sand), Se had some positive effects on the growth of sprouts. The peak sprouting capacity was reached after 8 months of storage. The highest Se enrichment of tubers had some positive effect on the free putrescine content in sprouts. However, the better growth of sprouts was not consistent with the growth vigour of the seed tubers and yield produced. Selenium had no significant effect on the malondialdehyde (MDA) or on the concentration of soluble sugars and starch. No significant effect of added Se on the early growth, stem and tuber numbers and yield parameters was observed. Irrespective of the level of Se added, the highest yield was harvested from plants produced with seed tubers stored for 6 months. Our results indicate that Se had some positive effects on the growth of sprouts, but it had no consistent effect on the growth vigour of seed tubers.