, Food, and Rural Affairs Guelph, ON Pate, J.S. 1980 Transport and partitioning of nitrogenous solutes Annu. Rev. Plant Physiol. 31 313 340 Plotkowski, D. Cline, J. 2021 Evaluation of selected cider apple ( Malus domestica Borkh
Neal Mays, Curt Richard Rom, Kristofor R. Brye, Mary C. Savin, and M. Elena Garcia
soil erosion ( Carter, 2002 ; Karlen et al., 1992 ; Kemper and Rosenau, 1986 ). Surface crusting and erosion may be reduced or eliminated in orchards with application of non-living groundcover mulches. Mulches useful for organic apple ( Malus
Cecil Stushnoff, Philip L. Forsline, Leigh Towill, and John Waddell
Cryopreservation of dormant buds has potential to provide back-up conservation of vegetatively propagated genetic resources for fruit crop species. This system may be useful where clonal integrity must be maintained and where it is desirable to rapidly recover plants with flowers for crossing purposes. In 1988, a pilot project involving the National Clonal Apple Repository at Geneva, NY and the National Seed Storage Laboratory, Fort Collins, CO, was initiated to test handling protocols as a prelude to establishing a cryopreservation backup system for apple genetic resources. Sufficient buds have been cryopreserved to permit viability evaluation after 1 month, 1, 2, 3, 4, 5, 10, 15, 20, and 25 years storage in liquid nitrogen vapor phase storage (-150 C]. Recovery of dormant buds collected 12/12/88 and 02/06/89 after one month in LN2 was 36% and 35%, respectively, for eight different taxa. After one year in LN2, recovery was 50% and 48% for the same taxa. The difference was attributed to improved handling during dehydration prior to patch budding for viability estimation. In 1990, recovery after 1 month in LN2 was 38% for six different cultivars. The response to controlled acclimation and desiccation for 15 taxa will be presented.
Xuetong Fan, J.P. Mattheis, M.E. Patterson, and J.K. Fellman
Several strains of Fuji apples were harvested weekly from September through October in 1990 and 1991, and evaluated for maturation and quality after 1 and 7 days at 20 °C following harvest and storage in atmospheres of 0.5%, 1.0%, 2.0% O2 and air. Results showed that Fuji apples have very low ethylene production rates and little firmness loss during maturation. A change in the postharvest respiration pattern preceded the increase ethylene synthesis. Oxygen concentration during storage directly affected apple respiration rate after removal from storage. Ethylene production rates and internal ethylene concentrations indicated that the apples were still in the preclimacteric stage after 7 to 9 months storage at 0.5%, 1.0%, or 2% O2. Fuji apples develop watercore and tend to have a particular type of corebrowing during maturation on the tree, or during and after storage. The cause is unknown.
Xiang Shen*, Zhenlin Wei, and Ling Guo
`Pingyitiancha' has good agricultural traits and is an important rootstock for apples. It was studied for Kam, Cef and Carb concentrations, precultural times, active medium of A.tum, Ca++ concentration, mixed inoculation times of AgNO3, and PVP delay selection times for getting transgenic `Pingyitiancha' stock with more resistance to drought and salt. It was demonstrated that the highest transformation frequency was obtained with 200 mg·L-1 Cef as an A.tum restraining antibiotic, 8 mg·L-1 Kam as a selection antibiotic, GCJ8 active medium, a precultural of 2 days, 5 Ca++ concentrations in preculture and coculture medium compared with standard MS medium, immersed in A. tum as OD600 for 0.5 to 1 min., 4 mg·L-1 AgNO3 and 0.7% PVP as an anti-oxidation compound to reduce hydroxybenzene oxidation and delay selection for 5 days by using `Pingyitiancha' apex shoots as explants. Using mediate of A. tum strain LBA4404 under conditions mentioned above and same explants, the HVA1 gene were transformed into `Pingyitiancha' under the control of CaMV35S promoter and obtained Kam resistance regeneration plants. Six transgenic plants were confirmed by PCR and subsequent dot blot methods.
Jacques J. Crabbe
The flushing behavior of shoot growth and its consequences on shoot differentiation are important features in fruit tree development, with regard to flowering ability. In this respect, two different approaches were applied to young `M26' apple trees. First, poorly branched 2-year-old trees were headed back, either in the second-year or in the first-year wood, at different times from right before to 6 weeks after budbreak. Early pruning resulted in rapid and prolonged regrowth, with a final very similar shaping of the tree to that of the intact controls. Late pruning, in contrast, leads to a two-step reaction (late spring and summer flushes), sometimes stronger on 2-year-old than on 1-year-old wood. In a second experiment, buds and young shoots were sampled on pruned trees in locations where they could be supposed to remain short shoots or grow long, with one or two flushes. They were weighed, their leaves and internodes measured, and the plastochron evaluated. During budbreak and the first month afterwards, shoot differentiation appears achieved. The primary difference between long and short shoot types does not consist in faster internode elongation but, rather, in faster production (reduced plastochron) of larger leaves.
Manfredo J. Seufferheld, Cecil Stushnoff, and Philip Forsline
Cryopreservation of mature dormant vegetative buds is a useful method to preserve germplasm of a large number of cold hardy apple cultivars. However, cold tender cultivars have proven to be much more difficult to cryopreserve. Eight cultivars were harvested in September 1993 at Geneva, NY before developing cold hardiness naturally. The twigs were encapsulated with 5% alginate and treated with stepwise imbibition of 0.5 to 1.0 M sucrose. The samples were desiccated over glycerol at 0C. Half of the samples were plunged directly into liquid nitrogen (IN) and the other half were first cooled slowly to -30C. The twigs that had been exposed to prefreezing conditions showed the highest survival (20 to 100%). The samples that were plunged directly in LN survived poorly (0 to 20 %). Samples without encapsulation and no sucrose imbibition had 0% survival. We conclude that this protocol opens up the possibility to expand cryopreservation of cold tender apple cultivars, presently grown only in field gene banks, at great expense and inconvenience.
Wenbin Zhang, Junru Zhang, and Xulan Hu
Adriana C. de M. Dantas, Gerson R. de L. Fortes, Sergio D. dos Anjos e Silva, and João Baptista da Silva
This work aimed to evaluate apple rootstock somaclones by characterizing the genetic variability among them. The isoenzymatic systems were used for analyzing variability as follows: FAC (acid phosphatase), PRX (peroxidase), and 6-PGD (6-phosphogluconate dehydrogenase). The migration were performed by applying a potential difference around 10 volt/linear cm. A data matrix was built so that the genotypes were placed in the lines and the bands in the columns. The scores were attributed as follows: band present (1) and band not present (0). By the gel analyses in relation to the presence/absence and band intensity, we observed marked differences among the somaclones and within somaclones as well. In the peroxidase system a higher band polyimorphism was detected with 18 enzymatic patterns. The group analyses for the 73 apple somaclones revealed a large variability through the enzymes (18 peroxidases, 8 FAC, and 6 6-PGD), which were classified into two groups. Group I was represented by M.7 somaclones with seven subgroups with 43% similarity among the clones. Differences among M.9 and M.111 cultivars and two clones referred to as M9b and M925 were fitted within somaclones M.111. The remaining somaclones of cultivar M.9 showed a higher variability bearing 43 subgroups. Clones M929, M930 and M932 presented 100% similarity.
Frank Cheng, Norman Weeden, and Susan Brown
The ability to pre-screen apple populations for fruit color at an early seedling stage would be advantageous. In progeny of the cross `Rome Beauty' × `White Angel' red/yellow color variation was found to be highly correlated with the genotype at Idh-2, an isozyme locus that was heterozygous in both parents. We postulate that the red/yellow color variation was produced by a single gene linked to I&-2 and also heterozygous in both parents. This population was also screened with over 400 primers to detect randomly amplified polymorphic (RAPD) markers for fruit color. DNA extraction procedures were developed for bark, and DNA was extracted from bark samples and leaves. Red and yellow fruited individuals were examined in bulk. Several markers have been found that are linked to red color. A high density map is being constructed in this region. These markers are being examined in other crosses segregating for fruit color. The application of these markers will be discussed in relation to the inheritance and manipulation of fruit color.