Relationships among estimates for the length of bud dormancy over a wide range of cultivars of Malus × domestics Borkh. and related Malus spp. are reported. Flower bud dormancy state was estimated after fitting quadratic models for the number of days for 50% terminal budbreak (D50), bud development stage (BDS), and percent terminal budbreak (BB) after 21 days of forcing as a function of chilling unit (CU) accumulation. Cultivar, linear, and quadratic components of regression, as well as all interactions, were significant for D50, BDS, and BB when regressed against CU accumulation. Consequently, cultivars differ not only as to when changes in “dormancy intensity take place, but also in the patterns and rates at which these changes proceed. The number of CU needed to reach arbitrary stages of each characteristic at the end of dormancy was calculated and compared for all genotypes. Rates of CU accumulation until BB, BDS, and D50 reached 50%, 1.5 and 15 days, respectively, were well-correlated. These CU values were considered the end of bud dormancy or genotype chilling requirement (CR). Estimations of D50 were less variable and less subjective, and a wider range of data points could be used in the analysis. In addition, values for D50 can indicate the growth potential of buds when other indices do not show changes. A few sampling times during the dormant season may give a preliminary idea about the CR of a given genotype.
Roberto Hauagge and James N. Cummins
Gayle M. Volk, Christopher M. Richards, Ann A. Reilley, Adam D. Henk, Philip L. Forsline, and Herb S. Aldwinckle
Seeds and scionwood of Malus sieversii Lebed. have been collected from wild populations of apple trees in Kazakhstan. Seedlings and grafted trees were planted in the orchards at the U.S. Dept. of Agriculture Plant Genetic Resources Unit in Geneva, N.Y. We developed core collections to capture the genetic and phenotypic diversity represented in the trees from each of two of the Kazakhstan collection sites. These core collections capture more than 90% of the genetic diversity of the original populations, as determined using seven unlinked simple sequence repeat markers and 19 quantitative traits. Since phenotypic evaluations of these materials have been completed, the 35 trees within each population will be used as parents in crosses so that the genetic diversity in the orchard populations can be captured as seed for long-term ex situ conservation. This strategy of storing seeds, rather than maintaining costly field collections, could be applied to other collections of wild plant materials in the National Plant Germplasm System.
Dorcas K. Isutsa and Ian A. Merwin
We tested 40 seedling lots and 17 clonal accessions—representing 941 genotypes and 19 species or interspecific hybrids of Malus—for their resistance or tolerance to apple replant disease (ARD) in a mixture of five New York soils with known replant problems. Total plant biomass, root necrosis, root-infesting fungi, and root-lesion nematode (RLN; Pratylenchus penetrans Cobb) or dagger nematode (DN; Xiphinema americanum Cobb) populations were evaluated in apple seedlings and clones grown for ≈60 days in the composite soil. In addition to phytophagous nematodes, various Pythium, Cylindrocarpon, Fusarium, Rhizoctonia and Phytophthora species were isolated from roots grown in the test soil. Plant growth response was categorized by a relative biomass index (RBI), calculated as total plant dry weight in the pasteurized field soil (PS) minus that in an unpasteurized field soil (FS), divided by PS. Nematode reproduction on each genotype was defined by a relative reproduction index (RRI), calculated as final nematode populations in roots and soil (Pf) minus initial soil populations (Pi), divided by Pi. The RBI, RRI, and other responses of accessions to ARD soil were used to rate their resistance, tolerance, or susceptibility to apple replant disease. None of the accessions was completely resistant to ARD pathogens in our test soil. Seedling accessions of M. sieversii Roem. and M. kirghisorum Ponom. appeared to have some tolerance to ARD, based upon their low RRIs and RBIs. Three clonal rootstock accessions (G.65, CG.6210, and G.30), and four other clones (M. baccata Borkh.—1883.h, M. xanthocarpa Langenf.—Xan, M. spectabilis Borkh.— PI589404, and M. mandshurica Schneid.—364.s) were categorized as tolerant to ARD. The disease response of other accessions was rated as susceptible or too variable to classify. We concluded that sources of genetic tolerance to ARD exist in Malus germplasm collections and could be used in breeding and selecting clonal rootstocks for improved control of orchard replant pathogens.
M.E. Garcia and Linda A. Boccuzzo
Hardiness testing of the wood of deciduous fruit trees has been conducted using a variety of techniques. In our studies, the objective was to determine an efficient method of determining freezing injury for apple (Malus × domestica Borkh.) wood. We tested 1-year old wood of two cultivars: Liberty and RedMax. The wood was tested over the course of 2 years (1998 and 1999). Collection began in the late fall and continued throughout the winter (until it was determined full hardiness had been achieved) and then again in the early spring. The wood was cut into 1-cm sections and frozen. The artificial freezing was conducted in an ethanol bath, with the temperature lowered at 5 °C/h. Samples were removed in 3-min intervals. After freezing, the wood was acclimated to 4 °C for 12 h. Three tests were conducted to determine the hardiness/injury to the tissues. The tests used were: discoloration, callus growth and vital staining (with 2,3,5-triphenyltetrazolium chloride). This was a split block design with samples collected randomly from each tree. Four replicates (12 trees) of each cultivar were tested. Results showed that the callus test predicted the same LT50 as the other two tests, discoloration and vital staining. Discoloration was not easy to differentiate and was the most time-consuming. The callus grown by the apple wood was easily formed and distinguished. The callus test does not require the tetrazolium stain; therefore, one less step was needed in comparison to the vital staining test. This reduced testing time by over 6 h.
Joseph Postman, Gayle Volk, and Herb Aldwinckle
inaequalis (Cke.) Wint. is an important fungal disease worldwide that results in symptoms on both apple leaves and fruit. Fruit with scab symptoms can be unmarketable, except in some niche outlets. In the GRIN database, scab susceptibility of Malus
Edwin J. Reidel*, Brian G. Ayre, E. Robert Turgeon, and Lailiang Cheng
Sorbitol (d-glucitol) is the major end product of photosynthesis in apple (Malus domestica Borkh.), as well as the predominant phloem-translocated carbohydrate. The mechanism by which sorbitol is phloem-loaded for transport to heterotrophic sink tissues is unknown. We hypothesized that a plasma membrane-bound H+/sorbitol symporter mediates apoplastic phloem-loading of sorbitol. To discover genes potentially encoding sorbitol transporters, a cDNA library was constructed from mature `Gala' apple leaves. A homologous probe was synthesized via PCR with primers were designed against the cherry fruit sorbitol transporter, PcSot1, and using library lysate as template. From an initial plating of approximately 5 × 105 clones, twelve positives were identified after three rounds of hybridization screening. Following single-pass, 5' end sequencing, the clones were sorted into four contiguous sequences. One clone was chosen from each contig for complete sequencing. The four clones, provisionally named MdSOT1-4 (Malus domesitca Sorbitol Transporter), potentially encode full-length cDNAs for sorbitol transporters: Translated-BLAST searching (blastx) revealed that the open reading frames encode the complete Pfam sugar transporter domain, and the most significant alignments are with sequences encoding known- and putative polyol and sugar transporters.
Shiow Y. Wang, Miklos Faust, and Michael J. Line
The effect of Indole-3-acetic acid (IAA) on apical dominance in apple (Malus domestica Borkh.) buds was examined by studying changes In proton density (free water) and membrane lipid composition in lateral buds. Decapitation induced budbreak and enhanced lateral bud growth. IAA replaced apical control of lateral bud paradormancy. Maximal inhibition was obtained when IAA was applied immediately after the apical bud was removed. Delaying this application weakens the effect of IAA. An increase in proton density in lateral buds was observable 2 days after decapitation, whereas the change in membrane lipid composition occurred 4 days later. Decapitating the terminal bud induced an increase in membrane galacto- and phospholipids. and the ratio of unsaturated to corresponding saturated fatty acids. Decapitation also induced a decrease in the ratio of free sterols to phospholipids in lateral buds. Application of IAA to the terminal end of decapitated shoots inhibited the increase of proton density and prevented changes in the membrane lipid composition of lateral buds.
Q. Liu, S. Salih, J. Ingersoll, R. Meng, L. Owens, and F. Hammerschlag
Transgenic `Royal Gala' apple (Malus × domestica Borkh.) shoots were obtained by Agrobacterium-mediated gene transfer using the plasmid binary vector pGV-osm-AC with a T-DNA encoding a chimeric gene consisting of a secretory sequence from barley-amylase joined to the modified cecropin MB39 coding sequence. Shoots were placed under the control of a wound-inducible, osmotin promoter from tobacco. The integration of the cecropin MB39 gene into apple was confirmed by Southern blot analysis. The transformation efficiency was 1.5% when internodes from etiolated shoots were used as explants and 2% when leaf explants were used. Both non- and transgenic tetraploid plants were produced by treatment of leaf explants with colchicine at 25 mg·L-1, and polyploidy was confirmed by flow cytometry. Of the diploid transgenics, three of seven were significantly more resistant to Erwinia amylovora than the non-transgenic `Royal Gala' control. Also, in one instance, a tetraploid transgenic was significantly more resistant than the diploid shoot from which it was derived.
Mekjell Meland and Clive Kaiser
‘Summerred’ apples (Malus domestica Borkh.) are highly susceptible to biennial bearing if not properly thinned. This results in erratic yields and also affects fruit quality adversely. Between 2003 and 2005, ‘Summered’/‘M9’ trees were treated with ethephon at concentrations of 250, 375, and 500 mg·L−1 when most king flowers opened (≈20% bloom) or at concentrations of 500, 625, and 750 mg·L−1 when the average fruitlet size was 10 mm in diameter. The experiment was conducted with 2.5-m height slender spindle trees sprayed to the point of runoff with a hand applicator only when temperatures exceeded 15 °C. Within 2 weeks after the second application, fruit set was reduced linearly with increasing concentrations of ethephon to less than one fruitlet per cluster at the highest concentrations used. Most thinning treatments reduced fruit set significantly compared with unthinned trees. Fruit numbers per tree decreased significantly with increasing ethephon concentrations, and the highest concentrations of ethephon applied during bloom or when the average fruitlet size was 10 mm in diameter resulted in overthinning. Yield results confirmed the fruit set response in which yield reductions were significant at the highest concentrations of ethephon (2.1 kg/tree) compared with hand-thinned trees (7.3 kg/tree) in 2005. All thinning treatments resulted in higher percentage of fruits larger than 60 mm diameter compared with unthinned control fruit. Thinning resulted in significantly higher soluble solid contents, and this was especially so for hand-thinned trees. Other fruit quality parameters like yellow–green background color did not show a clear response to thinning. Return bloom was, however, improved on all thinned trees. It is recommended that ethephon be applied at a rate of 375 mg·L−1 when king flowers open or at a rate of 625 mg·L−1 when the average fruitlet size is 10 mm in diameter. This thins ‘Summerred’ apples to a target of approximately five fruits/cm2 per trunk cross-sectional area or 50 to 70 fruits per 100 flower clusters without impacting on fruit quality, yield, or return bloom the next year.
James Mattheis and David R. Rudell
storage procedures. ‘Honeycrisp’ ( Malus × domestica Borkh.) apples from a commercial orchard in central Washington State were used in two consecutive seasons. Apples determined by the grower to be horticulturally mature were obtained the day of harvest