Influence of storage temperature on rate of potato tuber tissue infection caused byPhytophthora infestans (mont.) de bary estimated by digital image analysis

Summary Potato tubers were inoculated with two biotypes ofPhytophthora infestans then stored at 3,7, 10 and 15°C. Image analysis quantified average reflective intensity (ARI) of diseased tissue from cut surfaces of sample tubers. Tuber tissue infection and infection rate were measured by calculating Mean ARI of samples. Average tuber tissue infection and infection rate was minimal at 3°C (P.i.-US8 orP.i.-US1). Tuber tissue infection increased at temperatures >3°C, from 220 Mean ARI seven days after inoculation (dai) to 190–150 Mean ARI 50 dai (depending on cultivar and biotype ofP. infestans). Rate of tuber tissue infection caused byP.i.-US1 at 7°C was about zero in cv. Snowden but greater than −0.2 ARI day⁻¹ (cvs Russet Burbank and Superior). Rate of late blight infection in tuber tissue generally increased with temperature from −0.2 ARI day⁻¹ (at 7°C) in all cultivars to a maximum of −0.8 ARI day⁻¹ (10°C).     

Influence of post-harvest storage temperature and gamma irradiation on potato carotenoids

Summary A comparative study of nine Indian potato varieties showed a good correlation between their total carotenoid content and the tuber flesh colour. Regardless of varietal differences, carotenoid level showed an increase during storage at ambient temperature (25–30°C) and to a lesser extent at 2–4°C and 15°C. Tubers exposed to an irradiation dose of 10 krad for sprout inhibition showed decreased levels of carotenoids during storage, particularly at 15°C where 50% loss was observed after 6 months of storage. Irradiated tubers stored for seven months at 15°C, on reconditioning at 34–35°C for 6 to 12 days showed a 2- to 6-fold increase in their carotenoid content.     

Amylolytic activity in stored potato tubers. 2. The effect of low-temperature storage on the activities of α-and β-amylase and α-glucosidase in potato tubers

Summary Tubers of the potato cultivars Record, Wilja, Pentland Dell and Brodick (formerly clone 137371) were sampled before and after storage at either 4°C or 10°C. Reducing sugar content stayed constant during storage at 10°C in all four cultivars but rose greatly during the first 6–12 weeks of storage at 4°C in Record, Wilja and Pentland Dell but not in Brodick. Amylolytic activity was determined after 5 weeks storage using blockedp-nitrophenyl maltoheptaoside as substrate for α-amylase,p-nitrophenyl maltopentaoside as substrate for β-amylase, andp-nitrophenylglucopyranoside as substrate for α-glucosidase. The values obtained from tubers stored at 4°C were higher than those from tubers stored at 10°C, the differences being much less in Brodick than in the other three cultivars.     

The effect of temperature and light during storage of young seed potatoes on initial plant development at early plantings

Summary Young seed tubers of several cultivars were exposed to storage temperatures of 4–24°C in light and dark intended to optimise their growth vigour following early plantings. In five experiments during four autumn and winter periods, the effects of storage conditions on subsequent initial plant development in the glasshouse were studied. Storage of seed potatoes for 2 months at temperatures of 12°C or higher greatly increased early plant development of five cultivars following early plantings. Light during storage had a favourable effect, but desprouting before planting was greatly disadvantageous.     

Shortening dormancy of seed potatoes by storage temperature regimes

Summary Four experiments (three with four cultivars, one with twenty cultivars) investigated the effect of different storage temperature regimes on the duration of dormancy of seed potatoes harvested immature. Regimes included constant temperatures (18 and 28°C), hot pre-treatments (20 days at 28°C and subsequently 18°C) and cold pre-treatments (20 days at 2°C and subsequently 18°C). Compared with 18°C, storage at 28°C slightly prolonged dormancy of some cultivars with a genetically short dormancy and shortened dormancy by up to 45 days in cultivars with a long dormancy. Some tubers of one cultivar lost their ability to sprout after storage at 28°C for 90 days. A hot pre-treatment shortened dormancy by 2–3 weeks on average, for all cultivars examined. A cold pre-treatment shortened dormancy by 2 weeks on average in some cultivars with a short dormancy and in all cultivars with a long dormancy.     

The effect of potato seed tuber age and soil temperature on the phenomenon of non-emergence

Summary In three experiments seed tubers of cvs Jaerla, Bintje and Alpha, stored at 12 °C in the dark, were planted in glasshouses on various dates at soil temperatures varying from 8 °C to 28 °C to study the phenomenon of ‘non-emergence’ with ageing seed tubers. In general the tubers were desprouted before planting. At all plantings cv. Alpha produced normal plants. The cvs Jaerla and Bintje, however, showed high proportions of the ‘little potato’ phenomenon when planted in cold soil, and high proportions of decayed tubers more frequently in warm soil. When using physiologically older seed at later planting dates, both the range of soil temperatures became wider and the proportions of seed tubers experiencing both ‘little potato’ and decay increased.     

Effects of inoculum source and irrigation on black dot disease of potatoes (Colletotrichum coccodes (Wallr.) Hughes) and its development during storage

Summary In 1985 and 1986 plots were planted with seed tubers affected with black dot and with healthy seed inoculated or not with cultures ofColletotrichum coccodes at planting. Half the plots were irrigated from shoot emergence to the end of July. Seed tubers rotted more often when they were diseased than when they were not and rotting was increased by irrigation; by contrast, up to 18 weeks after planting irrigation decreased infection of stem-bases, roots and tubers. Tuber infection, first recorded in July, increased throughout the season and most rapidly from September, when the irrigation applied earlier increased disease. Soil-applied inoculum gave most disease in both years and tubers from healthy seed gave least in 1986 but as much as from diseased seed in 1985. Incidence and severity of black dot increased more during storage at 15°C than at 5°C and only on unwashed tubers.     

Post-harvest characteristics of potato minitubers with different fresh weights and from different harvests. II. Losses during storage

Summary Storage losses were studied in minitubers of cvs Agria and Liseta, using five fresh weight classes (<0.50 g, 0.5–0.99 g, 1.00–1.99 g, 2.00–2.99 g, ≥3.00 g), and three successive harvests of the same plantlets. After each harvest, tubers were dired at room temperature (1 day), curred at 18 °C (13 days) and stored at 2 °C (540 days). Two kinds of storage losses were considered: (a) losses of entire tubers because of deterioration, and (b) fresh weight losses of the other tubers. Both kinds of losses were higher in cv. Liseta, in tubers with lower fresh weights and in tubers from the first harvest. Almost all minitubers ≥0.5 g from later harvests and from both cultivars survived storage for 1.5 years. Deterioration occurred mainly from 6 to 12 months of storage. Tubers which deteriorated during cold storage had already shown high weight losses during curing.     

Leak syndrome of potato in Tunisia caused byPythium aphanidermatum andPythium ultimum

Summary TwoPythium spp. were isolated from diseased tubers exhibiting rots at harvest, in summer stores and also in refrigerated storage. Symptoms shared features described for both pink rot caused byPhytophthora erythroseptica and leak caused byPythium spp. The causal agents were identified asPythium aphanidermatum andP. ultimum by morphological and physiological observations and by fingerprinting using oomycete specific primers to amplify the internal transcribed spacer (ITS1) within ribosomal DNAs. The optimum temperatures for infection were 30°C forP. aphanidermatum and 25°C forP. ultimum, corresponding to the optimum temperatures for growth in vitro. The optimum concentration for infection of tubers inoculated by dipping in a suspension of oospores or hyphal swellings after wounding was found to be 10³ reproductive organs/ml, whereas the infection threshold was 10 reproductive organs/ml.     

Relation between growth conditions and dormancy of seed potatoes. 2. Effects of temperature

Summary In two indoor experiments under short day conditions, the effect of temperature during tuber bulking on dormancy of tubers was investigated for cvs Diamant and Désirée. Temperature treatments started after tuber initiation and lasted for 4 weeks, after which the haulm was removed. In Experiment 1, the day/night temperature regimes 18/12, 22/22, 26/18 and 32/12 °C (T18/12 etc.) were compared. In Experiment 2, three day temperatures (18, 24 and 30 °C) were combined with three night temperatures (12, 18 and 24 °C), resulting in nine treatments. The dormancy of cv. Diamant was shortest after very high day temperatures (30–32 °C), but intermediate day temperatures (22–26 °C) had no shortening effect compared to T18/12. Dormancy of cv. Désirée was not shortened, but rather tended to be prolonged by high temperatures (22–32 °C) during growth. High temperatures during growth resulted in more sprouts per tuber after dormancy had ended.     

The relationship between temperature and sprout growth in stored seed potatoes

Summary Sprout growth in a range of European cultivars was studied over two seasons at constant temperatures from 2 to 25°C, with an additional 33 (day)/22°C (night) treatment in the second season. There were only minor differences in the response of the cultivars and the optimum for sprout growth was at 15–18°C in all cases, when measured over an extended period, but initially sprout growth was more rapid at 23–25°C. Sprout growth at 23–25°C was frequently arrested by sub-apical necrosis, and at these temperatures the sprouts remained short enough for the tubers to be planted by hand without desprouting.     

Evaluation of treatments with hot water,chemicals and ventilated containers to reduce microbial spoilage in irradiated potatoes

Summary Potatoes irradiated to control sprouting were dipped in: hot water (56°C, 5 min; 52°C, 10, 15 and 20 min); cold (25°C, 5 min) or hot (56°C, 5 min) salicylic acid (1000 and 2000 ppm); or sodium hypochlorite (0.1 and 0.2%, 5 min); or dusted with salicylic acid (1 and 2%), to try to reduce the incidence of bacterial soft rot (Erwinia sp.) during controlled temperature (10°C, 15°C) and ambient temperature (20–34°C) storage. All treatments, particularly hot water and hot salicylic acid dip, increased microbial spoilage, possibly as a result of handling damage during the treatments combined with the inhibition of wound periderm formation as a result of irradiation. Storing irradiated tubers in well ventilated containers reduced soft rot compared to storing them in sacks and after 6 months storage at 10, 15 and 20–34°C, 95, 90 and 77% respectively were healthy and marketable.     

The immediate effect of gamma irradiation upon the sugar content of potatoes previously stored at 2, 4.5, 6, 10 and 15.5°C

Summary The sugar content of samples of potatoes, cv. Majestic, was varied by storage for 4 weeks at 2, 4.5, 6, 10 and 15.5°C, before irradiation with 10 krad. With initial sucrose contents of 0.14–0.37% FW (tubers from 4.5–15.5°C) the marked temporary increase in sucrose, as reported previously, was observed, reaching a maximum after 3–7 days before falling rapidly to a level rather higher than in non-irradiated tubers. Tubers from 2°C, with 1.4% sucrose, showed an immediate drop in this after irradiation, succeeded within 3 days by a rise to values not significantly different from the controls. Irradiation caused a significant increase in reducing sugar content, for a period of up to 7 days in sweetened tubers, but for 21 days or more in unsweetened tubers. Previous storage at the different temperatures had some permanent residual effect upon the sugar content of the controls during subsequent storage for up to 90 days at 10°C.     

Seed potato quality as influenced by high temperatures during the growth period. 1. Effect of storage temperature on sprout growth

Summary In the Negev area of Israel potatoes are grown in two seasons of the year: spring and autumn. Locally grown seed of cv. Up-to-Date prepared for the autumn season are grown in the spring under high-temperature conditions during the last part of the growth period. The response to storage temperature treatments consisted of different degrees of sprouting. Temperatures that encouraged bud development (12–22°C) shortened the dormant period of the tubers by about a month, and usually there is clear apical dominance. However, increasing length of the apical bud was positively correlated with storage temperature. Partial loss of apical dominance was obtained when the tubers were held at a low temperature (4°C) for at least two months after lifting. After transfer of the tubers to high temperatures for another month, there were 3 or 4 sprouts per tuber. The physiological age of seed tubers developing in the semi-arid region is discussed. Contribution from the Agricultural Research Organization, Beit Dagan, Israel 1979 Series, No 300.     

The effect of temperature on the development of wilting and on progeny tuber infection of potatoes inoculated with South African strains of biovar 2 and 3 ofPseudomonas solanacearum

Summary Potato plants, after inoculation with a South African strain of biovar 2 or a strain of biovar 3 ofPseudomonas solanacearum were grown in growth chambers at temperatures ranging from 14/16°C (dark/light) up to 25/30°C. When grown at 14/16°C or higher, plants inoculated with the biovar 2 strain developed wilting symptoms and internal symptoms on progeny tubers and the disease was transmitted by the progeny tubers. When the plants were inoculated with the biovar 3 strain, wilting symptoms developed from 18/20°C, internal symptoms on progeny tubers from 20/22°C and the disease was transmitted by progeny tubers from plants grown at 16/18°C or higher.     

Effect of a continuous hot water treatment of potato tubers on seed-borne fungal pathogens

Summary The viability of five pathogens was decreased by treatment with hot water when tested in vitro.Polyscytalum pustulans was most sensitive andRhizoctonia solani least sensitive. Potato tubers were exposed to 55°C for 5 min in a commercial continuous hot water treatment plant using naturally contaminated seed tubers and tubers which had been inoculated by dipping in comminuted cultures. The frequency of eyes colonised byP. pustulans, Helminthosporium solani, andR. solani was reduced to virtually zero and the effect persisted on tubers subsequently stored at 4°C and at 15°C for up to 16 wk. Results withColletotrichum coccodes were inconclusive. Treatment suppressedPenicillium spp. which, however, rapidly recolonised the eyes during storage, leading to higher contamination levels in the treated than in the untreated tubers. With tubers inoculated withPhoma foveata, good control was achieved when the incubation period before treatment was 10 d but not when the period was 42 d.     

Variation in pathogenicity on potato tubers and sensitivity to thiabendazole of the dry rot fungusFusarium avenaceum

Summary The majority of isolates ofFusarium avenaceum caused dry rot on potato tubers; many were as pathogenic asF. coeruleum. Pathogenicity ofF. avenaceum was not related to the plant species from which the isolates originated. Tubers of potato cv. Cara were more susceptible than those of cvs Romano or Maris Piper. Temperature (5–15° C) had no effect on lesion depth but lesions tended to be slightly wider at the lowest temperature. Two isolates (of 61) from wheat and white lupin had a moderate level of resistance to thiabendazole. The results are discussed in relation to the control of dry rot in stored potato tubers.     

The effect of controlled atmosphere storage at 4°C on crisp colour and on sprout growth,rotting and weight loss of potato tubers

Summary After three weeks curing at 10°C, potato tubers cv. Record were stored at 4°C under different controlled atmospheres (CA) for six months to study the effect on crisp fry colour, sprout growth and rotting. Combinations of low levels of CO₂ (0.7–1.8%) and low levels of O₂ (2.1–3.9%) gave a significantly lighter crisp colour, low sprout growth and fewer rotted tubers compared with 0.9% CO₂ and 21.0% O₂. Tubers stored in these conditions. showed a significantly higher weight loss and shrinkage after reconditioning. High CO₂: low O₂ combinations during storage completely inhibited sprout growth and caused the darkest crisp colour, but after reconditioning tubers gave the same level of sprouting and crisps as light as the other CA combinations. Furthermore these combinations, especially CO₂ at 10 or 15%, increased the onset of rotting. Also our results showed that at low concentrations of CO₂ (0.7–1.6%), and low O₂ (2–2.4%) there was an increase in tuber rotting.     

Dormancy and sprout development of some South African potato cultivars during cold storage

Summary Observations were made on dormancy and sprout growth of nine potato cultivars stored at 3–4°C, 7–8°C and 11–12°C, respectively. Tubers of the cultivar Vanderplank had a very long dormant period (232 days at 3–4°C) and showed little sprout growth at 180 days. The cultivar Koos Smit had a very short dormant period (92 days at 3–4°C) and developed considerable sprout growth at the higher temperatures. The reaction of tubers of Up-to-date and BP₁ were approximately the same, and intermediate between those of Vanderplank and Koos Smit.     

Etablierung von Kartoffelsorten im Feld nach physiologischer Alterung der Pflanzknollen

Zusammenfassung Die physiologische Alterung der Pflanzknollen durch Lagerung bei überoptimalen Temperaturen (jahresunterschiedlich 16–29,5°C, 1988–90 vor dem Pflanzen abgekeimt, 1991 vorgekeimt wie Kontrolle) führte im Vergleich zur vorgekeimten Kontrolle im Mittel von 25 Sorten in allen Versuchsjahren zu einer Verminderung der Bestandesdichte und des Ertrages. Eine Gruppe von Sorten erwies sich in allen Jahren als relativ tolerant gegen die Alterung, eine andere als signifikant empfindlicher, dazwischen lag ein breites Mittelfeld mit zum Teil erheblichen Schwankungen in den Jahren. Die Reaktion der Sorten zeigte keine Beziehung zu ihrer Reifegruppe und ihrer Keimintensit?t, dagegen war die sortentypische Ertragsdepression nicht sehr eng, aber signifikant mit dem Schwund w?hrend der Lagerung korreliert.

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Summary Seed tubers were stored at above optimal temperatures. Mean temperatures varied during test years from 16 to 29.5°C (in 1988–1990 tubers desprouted before planting; in 1991 chitted tubers as in control; Table 1). This procedure of physiological ageing of seed tubers resulted in reduced plant density and lower yield compared to the chitted control in every year of the test period (average of 25 cultivars). The emergence was significantly delayed as compared to the control in all years (Table 2). Assessed for yield, the cultivars Désirée, Sanetta, Astilla and Andra showed a significantly higher degree of tolerance to warm storages (>80%, when compared to the control) than the cultivars Arkula, Dorisa, Karlena and Koretta (<25%; Table 3). Between these two extremes there was a large number of intermediate levels of tolerance, a result of fluctuating reactions of various cultivars to changing conditions in the years of the test period (Fig. 1). No correlation could be found between the cultivars' reactions and their maturity group or their sprouting behaviour. There was, however, for each cultivar a significant negative correlation between loss in weight through transpiration and respiration and plant density and yield (r=−0.55 and −0.54; Table 4). Plant density and yield were closely correlated (Table 4). The regressions between loss of plants and reductions in yields show that after seed tuber storage at higher temperatures a reduced yield must be expected even when plant density is not reduced (loss of plant 0%; Fig. 2). With complete stands, the use of physiologically aged seed tubers that were desprouted before planting (1988–1990) resulted in a reduction of yield of 17–20%; when old seeds were chitted as in control a loss in yield of 15% was calculated.