Effect of transplant container volume and growing season length on field performance of micropropagated potatoes

Micropropagation is a tissue culture technique adapted for the rapid multiplication of disease-free seed stocks. Procedures for propagating potatoes in the laboratory and acclimating plantlets in the greenhouse are available, but information on cultural practices for maximizing tuber yield of plantlets when transplanted to the field is lacking. Centennial Russet and Russet Burbank plantlets were transferred from culture jars to three sizes of transplant containers for establishment under greenhouse conditions before transplanting to the field. Length of field growing season was varied by using two transplant dates and two vine kill dates. Survival of field transplanted plantlets was above 95 percent in both 1983 and 1984. Cultural practices significantly affected the tuber yield of plantlets of both cultivars. Total yield and yield of tubers larger than 35 mm in diameter increased with increasing transplant container volume. Transplant container volume had no effect on the yield of tubers less than 35 mm in diameter. Highest total yields and tuber production per plantlet for both Centennial Russet and Russet Burbank were obtained from the longest growing season (early transplant date with late vine kill). Yield of Russet Burbank plantlets increased more in response to a longer growing season than did Centennial Russet.     

Use of jasmonate for conditioning of potato plantlets and microtubers in greenhouse production of minitubers

A two-year study was conducted to determine the effects of (1) jasmonic acid (JA) pre-treatment, (2) JA supplement in culture media, (3) cultivar (Amisk, Atlantic, Russet Burbank, Shepody, and Umatilla Russet), (4) light (0 h, 8 h), and (5) dormancy breaking treatment (Rindite, gibberellic acid) on greenhouse production of minitubers from microtubers andin vitro plantlets. The microtubers were produced under short day (8 h) light conditions and in darkness, from stock plantlets pre-treated with JA and untreated, and on tuberization media with or without JA.In vitro plantlets (the industry choice in nuclear seed potato production) of all five cultivars performed well, meeting the standard criteria for greenhouse production of minitubers. Production of minitubers from microtuber-derived plants of cvs Amisk, Russet Burbank, and Umatilla Russet was similar to that of plantlet-derived plants with regard to number of minitubers. Yields (weight), however, were lower than those from plantlets. Microtuber responses to JA varied with cultivar. Amisk produced the highest number of minitubers per plot from microtubers derived from JA pre-treated plantlets. Jasmonic acid-pretreated microtubers also gave significantly more minitubers in Russet Burbank and Umatilla Russet than the microtubers from other treatments. Shepody did not benefit from JA treatments and JA pre-treated Atlantic microtubers performed poorly, producing significantly lower yields of minitubers than other cultivars. Independently of cultivar, microtubers produced under 8-h photoperiod gave significantly higher yields of minitubers than microtubers produced in the dark. Dormancy release was the key factor influencing microtuber performance. Rindite proved to be a much more effective dormancy breaking treatment than gibberellin. JA conditioning of stock plants prior to tuberization is being proposed as a treatment in production of microtubers for greenhouse production of minitubers.     

Potato leafroll virus spread in differentially resistant potato cultivars under varying aphid densities

An action threshold of 3-10 green peach aphid,Myzus persicae (Sulzer), apterae per 100 lower leaves is recommended for use in Minnesota to prevent further spread of potato leafroll virus (PLRV) in potato,Solarium tuberosum L. This threshold was first developed and validated using the PLRV susceptible cultivar Russet Burbank. Here we report experiments to determine if higher aphid densities could be tolerated in PLRV resistant cultivars,i.e., Kennebec (moderately resistant) or Cascade (highly resistant), without an increase in PLRV infection. Insecticidal sprays were applied to plots when predetermined target aphid densities, based on number of apterae per 100 leaves, were reached: 3, 10, 30, and 100 (Russet Burbank); 10, 30, 100, and 300 (Kennebec); and 30, 100, 300, and 1000 (Cascade). The response variable was the average percentage of PLRV infected plants. Overall mean cumulative aphid-days and percent PLRV infection were 617 and 23.5% for Russet Burbank, 1,296 and 10.2% for Kennebec, and 4,816 and 9.5% for Cascade. For each cultivar, the highest target aphid density tolerated without an increase in PLRV spread was determined by comparing PLRV infection in plots sprayed on predetermined thresholds to PLRV infection in plots where aphids were rigorously controlled. This maximum density was 10 apterae per 100 leaves for Russet Burbank and 300 apterae per 100 leaves for Cascade. Results using Kennebec were ambiguous, but Kennebec was always more resistant to PLRV than Russet Burbank. Excised leaflet tests showed that the cultivars did not differ in resistance to green peach aphid. It appears that action thresholds based on green peach aphid apterae can be different depending upon the inherent PLRV-resistance of the cultivar.     

Translocation and mechanical spread of a Minnesota isolate of potato virus S in potatoes

Potato cultivars Norland, Kennebec, and Russet Burbank were inoculated with a Minnesota isolate of potato virus S (PVS) in the field. The incidence of secondary infection, measured by enzyme-linked immunosorbent assay (ELISA), indicated that significantly more PVS infection occurred in Russet Burbank than Norland or Kennebec, and that Norland had significantly more infection than Kennebec (P≤ 0.01). Mature plant resistance was not observed. Rapid reinfection of PVS-free seedlots resulted from inoculum point-sources when routine cultivation practices were followed. Reinfection rates were significantly greater for seedlots grown at Grand Forks, ND, when compared with seedlots grown at Becker, MN, during both years of the study (P≤ 0.01). After two years in the field, reinfection rates for Norland (71.8%) and Russet Burbank (73.0%) did not differ significantly, but were significantly greater than the reinfection rate for Kennebec (29.5%) (P≤ 0.01). In greenhouse-grown plants, PVS moved out of rub-inoculated leaves within 24 hr, however, 13 and 20 days were required before PVS was detected with ELISA in foliage above and below the inoculated leaf, respectively. The frequency of PVS detection was significantly greater in foliage above the inoculated leaf compared to foliage below the inoculated leaf (P≤ 0.05). Translocation of PVS from inoculated leaves to daughter tubers occurred within 13 days for Russet Burbank and Norland and within 20 days for Kennebec.     

Manipulation of microtubers for direct field utilization in seed production

A two-year field study was conducted to determine the effects of jasmonic acid (JA), light (duringin vitro explant production andin vitro tuberization phases), and dormancy-breaking treatment on performance of microtubers in the production of seed tubers (pre-elite) in five potato cultivars. Microtubers were produced under short day (8-h) conditions and in darkness, from stock plantlets pre-treated with JA and untreated, and on tuberization media with or without JA. Microtuber performance was compared to invitro plantlets transplanted directly to the field. Yields of tubers from microtubers were 30% to 40% of those from plantlets. Microtubers of cultivars Amisk and Russet Burbank produced the highest yields of pre-elite tubers. Atlantic microtubers performed poorly in the field. JA pre-treatment of stock plantlets, prior toin vitro tuberization, enhanced seeds tuber production from microtubers in Russet Burbank and lowered in Shepody. JA presence in media duringin vitro tuberization significantly lowered production of tubers while exposure to 8-h light resulted in microtubers performing significantly better in the field than microtubers produced in the dark. Dormancy release was the key factor influencing microtuber performance. Unlike greenhouse studies, gibberellic acid (GA₃) was more effective than Rindite. A further refinement of the production and handling methods is required before microtubers can be recommended for field production of seed tubers.     

Effect of leaves on microtubers produced from potato single-node cuttingsIn Vitro

Microtubers are used to propagate, to store, and to transport potato clones. Culturing single-node explants from potato plantletsin vitro without subtending leaves was reported to result in plantlets with lower vigor and a higher coefficient of variation. The effect on microtuber productionin vitro of leaf area and the presence or absence of leaves on potato single-node cuttings was investigated as an extension of the above study. Stock plantlets of potato cvs Atlantic, Kennebec, Russet Burbank, and Shepody were cultured under a 16-h photoperiod. Single-node cuttings were excised and grown in a high-sucrose tuberization medium in darkness. Leaf area did not affect the frequency, size, or weight of microtubers of cvs Katahdin and Russet Burbank. The absence of leaves reduced microtuber diameter for Russet Burbank; whereas Atlantic, Kennebec, and Shepody were unaffected. Mean fresh weight of microtubers was reduced when leaves were removed for all cvs except Atlantic. No effect of the removal of the leaf was observed for mean dry weights of microtubers from all cvs, although microtubers from single-node cuttings without leaves accumulated significantly more percent dry matter than those with leaves. Rapid multiplication facilities may therefore wish to consider conserving resources such as media, vessels, and growth room space by culturing explants without leaves for the production of microtubers.     

Effect of short- and long-term exposure of seed tubers to low temperatures on the growth and yield of five potato cultivars

Trials were conducted in Alberta with Norchip, Norland, and Russet Burbank and in Ontario with Kennebec, Russet Burbank, Norchip, and Superior tubers to determine their response to short-term exposure to air temperatures of 0, ?1, and ?5 C and to long-term exposure to ?1, 0, 1,2, and 3 C. Exposure of seed tubers to ?1 C from 6 hours to 5 days did not affect growth characteristics or tuber yield of any of the five cultivars studied. Long-term (October–May) exposure to ?1 C in one study severely reduced emergence and tuber yield of Norchip (P<0.05). While the marketable yield of Russet Burbank was also reduced (P<0.05) by this treatment, Norland was not affected. Tubers of all cultivars exposed to air temperatures of ?3 or ?5 C for longer than 24 hours were severely injured and were not planted in the field trials at either location. In Alberta exposure of seed tubers of Norchip, Norland, and Russet Burbank to ?5 C for 6 and 12 hours caused a reduction (not significant) in yield. In Ontario, long-term storage at 1, 2, and 3 C and in combination with short-term (2 weeks) exposure to 0 or 10 C had no effect on growth or marketable yield of Norchip, Russet Burbank, Superior, and Kennebec seed tubers.     

Effects of sulphur dioxide and nitrogen dioxide on fourSolanum tuberosum L. cultivars

The effects of sulphur dioxide (SO₂) and nitrogen dioxide (NO₂), singly and in combination, on the shoot growth of four potato cultivars differing in maturity classification (Solanum tuberosum L. ‘Superior,’ ‘Norchip,’ ‘Kennebec, rs ‘Russet Burbank’) were determined in controlled conditions. Plants were exposed to 0.11 ppm SO₂ and/or 0.11 ppm NO₂ for 24 hours a day for 7 or 14 days. There were no significant differences in leaf growth of ‘Superior’ or ‘Norchip’ plants at 7 or 14 days. Stem dry weight was significantly reduced in ‘Superior’ only after 14 days in the mixture. ‘Kennebec’ and ‘Russet Burbank’ plants had significantly less leaf area, leaf fresh weight, and leaf water content after 14 days of exposure to the mixture, but there was no significant change in dry weight. Specific leaf weight was significantly increased in the mixture treated plants of both cultivars. The two earlier maturing cultivars, ‘Superior’ and ‘Norchip,’ were less sensitive to the SO₂ and NO₂ combination than the two later maturing cultivars, ‘Kennebec’ and ‘Russet Burbank’.     

Cultivar response to Fusarium storage rot as affected by two methods of seed origin propagation; Clonal selection andin vitro culture

Progeny tubers from seed potatoes originating from either a traditional clonal selection method or the more modernin vitro tissue culture method of propagation were tested for storage rot response following inoculation of three tuber sites with twoFusarium species. Significant differences were found among disease responses for the twoFusarium species and for the four cultivars tested. Disease symptoms were less severe forF. solani var.coeruleum than forF. sambucinum. Fusarium sambucinum caused less disease in Superior than Kennebec, Russet Burbank and Sebago. Seed propagation method did not significantly affect disease response except for one case;in vitro culture of Kennebec had less disease due toF. sambucinum at the tuber side inoculation site than clonal selection. Kennebec and Superior inoculatedF. sambucinum had significant differences with respect to the number of years of field propagation for the tuber side inoculation site and for the tuber mean rot index. Significant differences in number of years of field propagation were also found for eye-ends of Superior tubers and stem ends of Russet Burbank tubers inoculated withF. solani var.coeruleum.     

Potato cultivar response to late blight as affected by clonal selection andin vitro culture

Response to foliar late blight for Superior and Sebago was not affected by the two potato seed selection and multiplication methods. Kennebec and Russet Burbank potato plants derived throughin vitro tissue culture techniques had significantly more late blight damage on only 4 of 7 and 2 of 7 observation dates, respectively, than plants derived through a clonal selection system. In practical terms, the disease response differences between the two seed propagation methods were minimal. Similarly, disease response differences among the 2 and 3 years of field multiplication for Russet Burbank and Kennebec, respectively, did not demonstrate any significant disease response trends. In general,in vitro culture plots had slightly higher yields than clonal plots but only Kennebec had a significant yield response. The incidence of late blight storage rot was generally not significantly different but clonally selected Kennebec potatoes had significantly more disease than those produced throughin vitro culture.     

Parenchyma cell growth in potato tubers I. Different tuber regions

Enlargement rates of starch-storage parenchyma cells during growth of Kennebec and Russet Burbank potato cultivars were determined for cortical, perimedullary, and pith tissuues of bud ends, midsections, and stem ends of tubers. Average volumetric size of parenchyma cells increased 7 to 18x during growth of Russet Burbank tubers, with the greatest increases occurring in cortical and perimedullary cells of bud ends and midsections, and the least in stem ends and pith tissues. In Kennebec tubers parenchyma cells in both stem end and midsection increased only 5 to 8 x, whereas increases in bud ends ranged from 8 to 20 times. Cell enlargement to tuber enlargement ratios appproached unity early in growth of Russet Burbank tubers. As tubers increased beyond the 45 g size, cell enlargement and tuber enlargement rates were essentially equal. Calculations of cells per unit tissue volume agreed with ratio determinations. The timing of such unity appeared to be delayed in Kennebec tubers, and was not quite as pronounced as in Russet Burbank tubers. This may have been due to differences in growth rates of individual tubers in response to cultural conditions. In general, cells of harvestmature Kennebec tubers were about 60% as large as similar cells of Russet Burbank tubers.     

The transmission of Potato Virus S by the cutting knife and retention time of infectious PVS on common surfaces

The transmission of PVS by the cutting knife in potato cvs Norland, Kennebec and Russet Burbank was studied in the field and greenhouse. Field studies showed transmission to Norland via tuber infection was significantly less than for Kennebec and Russet Burbank (P = 0.01). However, significant cultivar differences were not found in the greenhouse (P = 0.05). Contamination of the cutting knife by cutting through sprouts resulted in significantly greater numbers of plants infected for cv Kennebec than when sprout contact was avoided (P = 0.05). Although the same trends were observed for cv Norland and Russet Burbank the differences were not significant (P = 0.05). Infectious PVS particles were readily recovered from materials commonly contacted during potato cultivation, storage and processing. Retention time of infectious PVS was usually greater when materials were held at 4°C and 100% relative humidity than at ambient greenhouse conditions. Retention times ranged from 0 hr (PVS not recovered) to 180 hr on unpainted wood. Results demonstrated the need for strict indexing and sanitation procedures during the production of PVS-free potato seed.     

Wound-healing and the effect of soil temperature,cultivars and protective chemicals on wound-healed potato seed pieces inoculated with seed piece decay fungi and bacteria

The effect ofFusarium solani (Fsc),F. sambucinum (Fs),Erwinia carotovora subsp.atroseptica (Eca), andE. carotovora subsp.carotovora (Ecc) inoculated singly and in combination (FscFs, FscEca, FscEcc, FsEca, FsEcc, and EcaEcc) on wound-healed potato seed pieces of the cultivar Kennebec was studied. Potato seed pieces wound-healed for 5 days at 13 C and approximately 100% relative humidity, inoculated with Fsc, Fs, Eca, Ecc and their combinations, and incubated for 10 days at 9 C were protected from Eca, Ecc, and EcaEcc. When wound-healed potato seed pieces were inoculated with Fsc, Fs, Eca, Ecc, and their combinations and planted in soil maintained at 7, 10, 15, 20 and 25 C, wound-healing protected seed pieces from all pathogens and their combinations in seed pieces held for 10 days at 10 and 15 C. When seed pieces of cultivars Atlantic, Kennebec, Norchip, Russet Burbank and Superior were inoculated with Fsc, Fs, Eca, Ecc, and their combinations, different levels of protection were observed: Russet Burbank had the highest level of protection, Atlantic and Kennebec were intermediate, and Norchip and Superior were slightly protected. Dusting mancozeb on wound-healed seed pieces before inoculation with Fsc, Fs, Eca, Ecc, and their combinations increased protection against all pathogens and their combinations by 39% or more compared to the nonchemical control.     

Cell wall thickness during growth of domestic and foreign potato cultivars

During growth of Russet Burbank tubers from less than 100 to over 250 g, thickness of parenchyma cell walls nearly doubled (1.9X) to slightly over 1 μ. Although affecting cell size at harvest maturity, different levels of N fertilizer and soil moisture had little influence on wall thickness. Wall thickness in Kennebec and Norchip increased to 0.9μ (1.7X), and in White Rose to slightly under 0.8 (1.2X). During the same growth, cell size nearly doubled in Russet Burbank. Cells of Kennebec, Norchip and White Rose averaged smaller than those of Russet Burbank at harvest maturity. Wall thickness and cell size showed similar relationships in foreign cultivars. Wall thickness in European varieties Bintje and Pimpernel was comparable to that of White Rose. Thickness in Atjimba closely approached that of Russet Burbank, and in Kamarz was similar to that of Norchip. Among South American cultivars, Doré had unusually thick walls (1.36μ), whereas those in Fruitella and Papa Bianca were between those of Norchip and White Rose. Bintje was comparable to domestic cultivars in tuber size, but all other foreign cultivars studied had medium to small tubers. Doré had unusually large cells for a small tuber. Differences in wall thickness may be due to differences in amounts of cell wall material, to differences in hydration properties of pectic components, or to combinations of both. Independently of wall thickness, the many primary pit fields in parenchyma walls may be a limiting factor in wall strength. The very thin pit membranes consist mainly of cellulosic microfibrils formed early in cell growth.     

Utilization of potatoes for life support in space v. evaluation of cultivars in response to continuous light and high temperature

Twenty-four potato (Solanum tuberosum L.) cultivars from different regions of the world were evaluated in terms of their responses to continuous light (24 h photoperiod) and to high temperature (30 C) in two separate experiments under controlled environments. In each experiment, a first evaluation of the cultivars was made at day 35 after transplanting, at which time 12 cultivars exhibiting best growth and tuber initiation were selected. A final evaluation of the 12 cultivars was made after an additional 21 days of growth, at which time plant height, total dry weight, tuber dry weight, and tuber number were determined. In the continuous light evaluation, the 12 selected cultivars were Alaska 114, Atlantic, Bintje, Denali, Desiree, Haig, New York 81, Ottar, Rutt, Snogg, Snowchip, and Troll. In the high temperature evaluation, the 12 selected cultivars were Alpha, Atlantic, Bake King, Denali, Desiree, Haig, Kennebec, Norland, Russet Burbank, Rutt, Superior, and Troll. Among the cultivars selected under continuous irradiation, Desiree, Ottar, Haig, Rutt, Denali and Alaska showed the best potential for high productivity whereas New York 81 and Bintje showed the least production capability. Among the cultivars selected under high temperature, Rutt, Haig, Troll and Bake King had best performance whereas Atlantic, Alpha, Kennebec and Russet Burbank exhibited the least production potential. Thus, Haig and Rutt were the two cultivars that performed well under continuous irradiation and high temperature conditions, and could have maximum potential for adaptation to varying stress environments. These two cultivars may have the best potential for use in future space farming in which continuous light and/or high temperature conditions may exist. However, cultivar responses under combined conditions of continuous light and high temperature remains for further validation.     

Performance of Dimethomorph + Mancozeb Applied to Seed Potatoes in Early Management of Late Blight (<Emphasis Type="Italic">Phytophthora infestans</Emphasis>)

Treating seed potatoes with contact fungicides prevents infection of Phytophthora infestans from tuber to tuber during handling but does not prevent field infections in the young plant. Dimethomorph (DMM) 9% + mancozeb 60% (Acrobat MZ, BASF) can cover both aspects due to the contact and systemic action of mancozeb and DMM, respectively. Experiments were performed under greenhouse and field conditions (three seasons and two locations) with cvs Kennebec, Shepody, Spunta, Russet Burbank, and Ranger Russet. Immediately after cutting, seed pieces were treated with Acrobat MZ at doses equivalent to 2, 3, and 4 kg ha⁻¹. At any dose, Acrobat MZ protected healthy seed tubers against P. infestans infections. Acrobat MZ (4 kg ha⁻¹) also protected the foliage of all cultivars against artificial inoculation of P. infestans, assessed by the detached-leaf method. These effects were observed up to 30 days after emergence in greenhouse experiments and up to 28 days after crop emergence under field conditions in two growing seasons. In cv Spunta, significant foliage protection was observed up to 35 days after field emergence whereas in seed tubers of cv Kennebec planted in sandy soils, significant foliage protection persisted longer. Additional evidence for acropetal translocation of Acrobat MZ in field crops was also found. With this strategy, there is no need to apply contact or systemic fungicides early in the season, and spraying costs and environmental risks are also reduced.     

Comparative levels of potato viruses S and Y infection of microplants and tuber-propagated plants in the field

The practice of transplanting microplants from tissue-culture to the field was compared to normal tuber propagation with respect to the transmission and translocation of potato virus S (PVS) and potato virus Y (PVY) to the daughter tubers of Red Pontiac, Shepody, Kennebec, and Russet Burbank cultivars in Prince Edward Island in 1984 and 1985. In general, the use of microplants to produce seed stocks appeared to increase the risk of infection with both viruses, although the results for tuber infection with PVY were only significant in one of the years.     

Textural quality of cooked potatoes: II. Relationship of steam cooking time to cellular strength of cultivars with similar and differing solids

The relationship of steam cooking time with cellular strength of cultivars Chieftain, Kennebec, Russet Burbank and White Rose was compared within and among solids concentrations. Nitrogen fertilization had no discernible effect on cell wall strength. Cell strength of Kennebec and Russet Burbank was similar regardless of solids concentration or cooking time. However, cell strength of Chieftain and White Rose differed with solids concentration and cooking time. Knowledge of cell strength and its characteristics with cooking time appear important for understanding the differences in textural quality that exists between cultivars.     

Utilization of potatoes for life support in space. V. Evaluation of cultivars in response to continuous light and high temperature

Twenty-four potato (Solanum tuberosum L.) cultivars from different regions of the world were evaluated in terms of their responses to continuous light (24 h photoperiod) and to high temperature (30 C) in two separate experiments under controlled environments. In each experiment, a first evaluation of the cultivars was made at day 35 after transplanting, at which time 12 cultivars exhibiting best growth and tuber initiation were selected. A final evaluation of the 12 cultivars was made after an additional 21 days of growth, at which time plant height, total dry weight, tuber dry weight, and tuber number were determined. In the continuous light evaluation, the 12 selected cultivars were Alaska 114, Atlantic, Bintje, Denali, Desiree, Haig, New York 81, Ottar, Rutt, Snogg, Snowchip, and Troll. In the high temperature evaluation, the 12 selected cultivars were Alpha, Atlantic, Bake King, Denali, Desiree, Haig, Kennebec, Norland, Russet Burbank, Rutt, Superior, and Troll. Among the cultivars selected under continuous irradiation, Desiree, Ottar, Haig, Rutt, Denali and Alaska showed the best potential for high productivity whereas New York 81 and Bintje showed the least production capability. Among the cultivars selected under high temperature, Rutt, Haig, Troll and Bake King had best performance whereas Atlantic, Alpha, Kennebec and Russet Burbank exhibited the least production potential. Thus, Haig and Rutt were the two cultivars that performed well under continuous irradiation and high temperature conditions, and could have maximum potential for adaptation to varying stress environments. These two cultivars may have the best potential for use in future space farming in which continuous light and/or high temperature conditions may exist. However, cultivar responses under combined conditions of continuous light and high temperature remains for further validation.     

Modification of potato microtuber dormancy during induction and growthin vitro orex vitro

Prolonged or highly variable dormancy can be a significant impediment to the efficient use of potato (Solanum tuberosum L.) microtubers by the seed industry. In the present study, reductions in microtuber dormancy duration were obtained in cultivars commonly used by the processing industry (Kennebec, Russet Burbank and Shepody). This was achieved by modifying microtuber induction media and applying various dormancy-release treatments after harvest, with or without prior storage. An 8 h photoperiod, instead of continuous darkness during microtuber induction and development, increased microtuber yield while reducing dormancy duration. Dormancy duration was also shortened by increased sucrose concentration during microtuber induction under an 8 h photoperiod. As sucrose was increased from 4 to 16% under an 8 h photoperiod, mean dormancy duration decreased by 86 d for Shepody, 65 d for Kennebec and 46 d for Russet Burbank. During theex vitro storage period, 24 h treatment with bromoethane vapor (from 0.22 ml liquid BE per L volume) or bromoethane vapor followed by a 3 d treatment of 60% CO₂/ 20% O₂/ 20% N₂ resulted in a rapid dormancy release of freshly harvested microtubers. These dormancy-releasing treatments significantly increased minituber yields under greenhouse conditions for all cultivars when compared to untreated controls. Increased minituber yields were also observed when dormancy release treatments were applied to microtubers after storage at 6 C for 8 weeks. The results demonstrate that microtuber dormancy duration can be manipulated during growthin vitro orex vitro. However, optimization may require cultivarspecific protocols