Search Results

You are looking at 31 - 40 of 71 items for

  • Author or Editor: David Byrne x
  • Refine by Access: All x
Clear All Modify Search
Free access

Jonathan W. Sinclair and David H. Byrne

Carbohydrate source of peach [Prunus persica (L.) Batsch] embryo culture media affects embryo growth and survival. The first objective of this study was to determine the effect of five carbohydrates (fructose, glucose, maltose, sorbitol, and sucrose) in Woody Plant Medium (WPM) on the germination and survival of peach embryos in vitro. Fructose, glucose, maltose, and sucrose in WPM resulted in better embryo germination and survival than sorbitol. Fructose (2% and 3%) produced greater survival than all other carbohydrates tested in smaller embryos (<10% ovule dry weight). However, sucrose was better than all other carbohydrates tested in the larger embryos (≥10% ovule dry weight). In addition, large embryos (>10% ovule dry weight) on fructose at 1% combined with glucose, maltose, sorbitol, or sucrose at 1% had equivalent or higher survival than did those on either 1% or 2% sucrose in conjunction with the same carbohydrates. Embryo survival on different carbohydrates varied with genotype. The second objective of this study was to determine the effect of three levels of MES buffer (0.0 mm, 4.5 mm, and 9.0 mm) on medium pH stability and embryo survival. MES buffer at 0.0 mm and 4.5 mm concentration produced significantly better embryo survival than 9.0 mm. The pH stability was better at MES 9.0 mm, however survival decreased significantly. Chemical name used: [2-(N-morpholino)-ethane sulphonic acid] (MES)

Free access

Young-ju Kim and David H. Byrne

Isozyme analysis has been used for cultivar identification, but little has been done with the genus Rosa. One hundred and sixty rose accessions (species, cultivars, and hybrids) were characterized for isozyme phenotypes using starch gel electrophoresis. Six enzyme systems were stained on three electrode buffer systems. ACP, MDH, and 6PGD were run on morpholine citrate (pH 6.1) and histidine (pH 5.7), PGI and PGM were run on histidine (pH 5.7) and lithium borate (pH 8.3), and SKDH was run on morpholine citrate (PH 6.1) and lithium borate (PH 8.3). The most variable isozymes were MDH and 6PGD. MDH and 6PGD revealed 10 and 9 bands, respectively. This study showed that isozyme variability exists in roses and can be useful in their classification into species groups.

Free access

David H. Byrne and Terry A. Bacon

Free access

David Shupert, David H. Byrne, and H. Brent Pemberton

Research with the Basye Rose Breeding and Genetic Program at Texas A&M University has developed rose populations to use to study the genetic nature of leaf, stem, and several other rose traits. The rose populations are from the backcross of Rosachinensis`Old Blush' to WOB (interspecific hybridization of the diploid parents Rosawichuariana `Basye's Thornless' and `Old Blush'). The qualitative trait of presence of stem prickles and the quantitative traits of stem prickle density and leaflet number were observed in three field locations. Two locations are in College Station, Texas, and one location in Overton, Texas. The qualitative trait of presence of stem prickles supports the reported monogenic modes of inheritance. The presence of stem prickles (dominant) had a segregation ratio of 1:1 for prickles: no prickles. Prickle density and leaflet number demonstrated a quantitative mode of inheritance. For prickle density the genotype was significant and environment was nonsignificant. For leaflet number the genotype/generation was significant and environment was nonsignificant. This shows that genotype influences prickle density and leaflet number expression. The genotype by environment interaction was nonsignificant for all traits.

Free access

Yan Ma, David H. Byrne, and David M. Stelly

Mitotic chromosome numbers and measurements were determined from enzymatically digested shoot tips for 14 species of Rosa, subgenus Hulthemia, Platyrhodon, and Rosa (the latter represented by sections Pimpinellifoliae, Cinnamoneae, Synstylae, Banksianae, Laevigatae, and Bracteatae). All were 2n = 14 or 2n = 28, as expected from previously published chromosome counts in Rosa. Arm lengths of chromosome pairs measured from digitized images were analyzed for similarity using a least-squares algorithm. On this basis, tetraploid species were compared to their diploid relatives. This study demonstrates the value of karyotypic data in combination with morphological and ecological information for examining the evolution of Rosa.

Free access

Natalie Anderson, David H. Byrne, Jonathan Sinclair, and A. Millie Burrell

Embryo culture techniques are employed to germinate seed of early ripening peach and nectarine [Prunus persica (L.) Batsch] cultivars. Generally, the embryos in these genotypes do not mature by the time the fruit matures, thus rendering normal stratification procedures ineffective. In 1998 and 1999, immature embryos from multiple peach genotypes were cultured in an embryo rescue medium (Woody Plant Medium, 3% sucrose, 0.065% agar) at 5 °C for 45 days in the dark. Embryos were then placed under lights at either a cool-temperature (18 °C in 1999 and 20 °C in 1998) or a warm-temperature (30 °C in 1999 and 28 °C in 1998) treatment with a photoperiod of 12 hours for germination and initial growth. After 2-4 weeks, embryos were rated for germination, root number, and top growth. The embryos incubated at the cool-temperature regime not only had better germination, but also had a higher rate of greenhouse survival.

Free access

Unaroj Boonprakob, David H. Byrne, and Dale M.J. Mueller

Actively growing shoots of peach [Prunus persica (L.) Batsch] were collected every 2 weeks throughout the 1989 growing season. The samples were sectioned longitudinally and transversely to observe axillary bud initiation, which occurred in all samples collected. Differentiation of axillary bud meristems from early season samples (mostly normal nodes) included apical and prophyll formation, with procambium connected to the stem procambium. Little to no differentiation of such structures occurred in the late-season samples (mostly blind nodes). Other results suggest that blind node formation is a consequence of a lack of bud differentiation rather than a failure of bud initiation.

Free access

Ockert Greyvenstein, Terri Starman, Brent Pemberton, Genhua Niu, and David Byrne

The decline of garden rose sales over the past 20 years can be partially attributed to the lack of material adapted to a wide range of landscapes, which includes adaptation to high temperature stress. Current methods for evaluating high temperature susceptibility in garden roses are based on field observations, which are time consuming and subjected to ever-changing environmental conditions. A series of experiments were conducted to optimize protocols and compare the use of chlorophyll fluorescence (CFL) and cell membrane thermostability (MTS) by way of electrolyte leakage as methods to screen for high temperature susceptibility. Immature leaves proved better than mature leaves for both CFL and MTS measurements, using either detached leaf or whole plant stress assays. MTS measured on immature leaves stressed in a water bath at 50 °C for 45 minutes proved most consistent in separating rose clones based on high temperature susceptibility. Stressing actively growing plants with flower buds of 2 mm in diameter in a heat chamber at 44 °C for 3 hours resulted in increased flower abscission and leaf necrotic lesions on more susceptible clones when compared with those that were heat tolerant. Combining MTS measurements from immature leaves stressed in a water bath with the flower abscission and leaf necrosis responses 10 days after stress in a heat chamber could be the first step to screen and select against the more susceptible clones in a garden rose breeding program. Power analyses suggest that the proposed MTS protocol would be efficient in detecting differences between clones when the difference in electrolyte leakage is greater than 10%.

Free access

Qianni Dong, Xinwang Wang, David H. Byrne, and Kevin Ong

Black spot disease, caused by the fungus Diplocarpon rosae Wolf, is one of the most serious diseases of garden roses. Both complete (vertical) resistance conditioned by dominant Rdr genes and partial (horizontal) resistance conditioned by multiple genes have been described. The use of resistant rose cultivars would reduce the demand of agrochemical applications. The characterization of 16 genotypes for resistance to black spot using two laboratory assays, the detached leaf assay (DLA) and the whole plant inoculation (WPI) approach, indicated that these techniques were well correlated. Thus, either method could be used to assess the resistance of the plants to black spot. Fifteen diploid hybrid populations from 10 parents segregating for partial (horizontal) resistance to black spot derived from Rosa wichuraiana ‘Basye’s Thornless’ (RW) were assessed for black spot resistance by quantifying the percentage of the leaf area with symptoms (LAS) and lesion length (LL) measured by the diameter of the largest lesion per leaf in DLAs. The narrow-sense heritability of partial resistance to black spot as measured by LAS and LL data of DLA was estimated to be from 0.28 to 0.43 when calculated with a genetic variance analysis and from 0.74 to 0.86 when generated from offspring–midparent regression. This suggests that the development of rose cultivars with high levels of stable partial resistance to black spot is a feasible approach for the rose industry.

Free access

Bruce D. Mowrey, Dennis J. Werner, and David H. Byrne

Eighteen isozyme systems were surveyed in the peach [Prunus persica (L.) Batsch.] plant introduction collection. Seven systems were polymorphic. Three previously unreported isocitrate dehydrogenase (IDH; EC 1.1.1.41), three malate dehydrogenase (MDH; EC 1.1.1.37) and two shikimate dehydrogenase (SDH; EC 1.1.1.25) banding patterns were detected in the clones. Isocitrate dehydrogenase was dimeric in structure, with two alleles present at a single locus. Malate dehydrogenase was dimeric in structure, with three alleles present at the fast locus, while a second locus was monomorphic. Shikimate dehydrogenase was monomeric, with one allele present in most clones, while PI 113452, PI 113650, and PI 117679 were heterozygous for a slow SDH allele. Electrophoretic evidence suggests PI 113452, PI 113650, and PI 117679 are peach × almond (P. dulcis Webb) hybrids, since they were heterozygous for alleles previously reported only in almond.