Search Results

You are looking at 21 - 30 of 62 items for :

  • Prunus amygdalus Batsch x
  • Refine by Access: All x
Clear All
Free access

Carlos Miranda, Luis G. Santesteban, and José B. Royo

The influence of the species in spring frost sensibility was determined for the Prunus species peach (P. persica (L.) Batsch), sweet cherry (P. avium L.), almond (P. dulcis (Mill.) Webb/P. amygdalus Batsch), japanese plum (P. salicina Lindl.), and blackthorn (P. spinosa L.). The confidence intervals for lethal temperatures of 10% (LT10) and 90% (LT90) bud injury were also determined. In 2000 and 2001, seven frost treatments were made for each one of the phenological stages comprised between B (first swell) and I (jacket split) in two cultivars per each species. The relationships between frost temperature and the proportion of frost damaged buds for each cultivar, year, and phenological stage were adjusted to linear regression models. The 95% confidence intervals were also calculated. The spring frost hardiness order of the species, from the least to most hardy, was as follows: sweet cherry, almond, peach, japanese plum, and blackthorn. Despite the highly homogeneous nature of the frost and bud characteristics, the temperature range for a given injury degree was quite broad, since the confidence interval's breadth for LT10 was as high as about 3 °C and as high as about 6 °C for LT90. Consequently, when critical temperatures are used in making decisions as to when to begin active frost protection, a prudent measure would be to take the temperature references from the upper limits in the confidence intervals.

Free access

Thomas M. Gradziel and Steven A. Weinbaum

The regulation of anther dehiscence by relative humidity (RH) was assessed for detached anthers and detached whole flowers from a limited selection of apricot (Prunus armeniaca L.), peach [P. persica (L.) Batsch], and almond [P. dulcis (Mill.) D.A. Webb, syn. P. amygdalus Batsch; P. communis (L.) Arcangeli, non Huds.] genotypes, as well as an almond X peach F2 progeny. Dehiscence was evaluated at 33, 64, 87, 93 and 97% RH for detached anthers, and at 33, 64 and 97% RH for whole detached flowers. Anther dehiscence was suppressed with increasing RH for all genotypes. Apricot anthers showed the greatest dehiscence at low RH and measurable dehiscence at high RH even when detached. Anther dehiscence in almond appeared more suppressed than in apricot at all RH levels tested, being completely suppressed by high RH in detached anthers. Peach genotypes exhibited the full range of variability between apricot and almond patterns. Evidence for transgressive segregation of RH-controlled anther dehiscence was observed in the occurrence of cleistogamy in an almond × peach F2 progeny. Rates of anther dehiscence were approximately linear with change in RH in detached anthers but exhibited a more buffered, step-wise response when detached whole flowers were tested. Results are consistent with field observations, and highlight the low but measurable risk of cleistogamy in these species, as well as opportunities to modify the breeding systems and crossing environments to facilitate controlled hybridization, and to reduce pollination vulnerability to adverse environments.

Full access

Joseph H. Connell

California almonds [Prunus dulcis, (Mill.) D.A. Webb, syn. Prunus amygdalus Batsch] are self-incompatible requiring cross-pollination to produce a commercial crop. Within seven known pollen groups, they also display cross-incompatibility. Coincidence of bloom between compatible cultivars is essential for cross-pollination. Since almonds are pollinated primarily by honeybees [Apis mellifera L.], arranging pollinizers in close proximity to one another promotes maximum pollen transfer. Almonds are frequently subject to inclement weather during their February bloom period. Strong honeybee colonies are better able to forage during marginal weather conditions than are weak colonies. Honeybee management can encourage pollen foraging and placement of colonies can affect flight activity and ultimately nut-set. Weather permitting vigorous honeybee flight activity is the most important factor for setting a good crop. Temperature also affects anther dehiscence, pollen germination, and pollen tube growth. The sooner an almond flower is cross-pollinated after opening, the greater the chance of fertilization and nut-set. Optimizing all of these pollination factors is therefore essential to achieve maximum production in almond orchards.

Free access

T. Caruso, P. Inglese, M. Sidari, and F. Sottile

Seasonal development of leaf area, leaf area index (LAI), dry matter, and carbohydrate content were measured from harvest 1992 to harvest 1993 in above-ground components of `Flordaprince' peach [Prunus persica (L.) Batsch] trees grafted on GF 677 (Prunus persica × Prunus amygdalus) and MrS 2/5 (Prunus cerasifera free pollinated) rootstocks, which widely differ in vigor. Whole trees were separated into fruit, leaves, shoots, 1-year-old wood and >1-year-old wood. Sampling dates were coincident with key fruit and tree developmental stages: dormancy, fruit set, pit hardening, and fruit harvest. Rootstock modified the vegetative vigor of the tree, the seasonal partitioning of dry matter, and starch content in above-ground components. Leaf area, LAI, and total above-ground dry matter were twice as high in the most vigorous combination (`Flordaprince'/GF 677), which gave the highest yield, but had the lowest harvest index. Rootstock vigor did not affect soluble sugar concentration in any of the canopy components. Starch content was greatest during dormancy and in the oldest wood of GF 677 trees. During fruit development, starch content rapidly decreased in 1-year-old wood and perennial components; at pit hardening it was four times greater in MrS 2/5 than in GF 677 trees. The vegetative-to-fruit dry mass ratio by pit hardening was 3:1 for MrS 2/5 and 9:1 for GF 677 trees. Competition with shoot growth apparently reduced fruit growth, particularly during Stage I and Stage II, as fruit size at harvest was significantly lower (17%) in GF 677 than in MrS 2/5 trees.

Free access

Qijing Zhang and Dajun Gu

morphotypes. Previously, Rehder (1990) divided Prunus into five subgenera: Prunophora (plum and apricot), Amygdalus (peach, nectarine, and almond), Cerasus (cherry), Padus (cluster cherry), and Laurocerasus (laurel cherry), and later, Ingram

Free access

Ashraf Abdallah, Miguel H. Ahumada, and Thomas M. Gradziel

Seed of California almond [Prunus dulcis (Mill.) D.A. Webb, syn. P. amygdalus Batsch, and P. communis (L.) Arcangeli, non-Huds.] genotypes contained very low saturated fatty acids, high monounsaturated fatty acids, and low polyunsaturated fatty acids. Kernel oil consisted primarily of five fatty acids: palmetic, palmetoleic, stearic, oleic, and linoleic. Linolenic acid was only present in amounts of <0.02% and only in a few samples. Small but significant differences among genotypes and sampling sites were found in the proportions of palmetic, palmetoleic, and stearic fatty acids. The major differences in fatty acid composition among genotypes was found in the proportions of oleic, a monounsaturated fatty acid, and linoleic, a polyunsaturated fatty acid. The proportion of oleic acid was highest, ranging from ≈62% to 76%, and was highly and negatively correlated with linoleic acid levels. Usable genetic variation and a significant genotype × environment interaction were identified for oil content and composition. The introgression of new germplasm from peach and related species does not appear to reduce oil quantity or quality, and may offer opportunities for further genetic improvement of kernel oil composition.

Free access

J.M. Alonso, J.M. Ansón, M.T. Espiau, and R. Socias i Company

Almond (Prunus amygdalus Batsch.) blooming date is determined by the temperatures during the dormancy period, from the onset of endodormancy to just before blooming. In this work we have developed a model, based on several years data, to estimate the mean transition date from endodormancy to ecodormancy in 44 almond cultivars covering the whole range of almond bloom, through the significance of correlation coefficients between the temperatures occurring during dormancy and the date of full bloom. The estimation of this date for each cultivar has allowed the calculation of its chill and heat requirements. It was found that most cultivars have chilling requirements between 400 and 600 chill units, whereas the span of heat requirements was wider, from 5500 to 9300 growing degree hours Celsius. Some cultivars show high chilling requirements and low heat requirements whereas others show opposite requirements. These differences confirm the wide almond adaptability to different climatic conditions and offer the possibility of being utilized in breeding programs. The good fit shown by the application of this model in the prediction of bloom time may sustain its application in chilling and heat requirement estimation in other fruit species if blooming dates and climatic data for several years are available.

Free access

F. Bartolozzi, M.L. Warburton, S. Arulsekar, and T.M. Gradziel

Almond [Prunus dulcis (Mill.) D.A. Webb, syn. P. amygdalus, Batsch; P. communis (I.) Archangeli] represents a morphologically and physiologically variable group of populations that evolved primarily in central and southwest Asia. California cultivars have been developed from highly selected subgroups of these populations, while new breeding lines have incorporated germplasm from wild almond and closely related peach species. The genetic relatedness among 17 almond genotypes and 1 peach genotype was estimated using 37 RAPD markers. Genetic diversity within almond was found to be limited despite its need for obligate outcrossing. Three groupings of cultivar origins could be distinguished by RAPD analysis: bud-sport mutations, progeny from interbreeding of early California genotypes, and progeny from crosses to genotypes outside the California germplasm. A similarity index based on the proportion of shared fragments showed relatively high levels of 0.75 or greater within the almond germplasm. The level of similarity between almond and the peach was 0.424 supporting the value of peach germplasm to future almond genetic improvement.

Free access

Ossama Kodad and Rafel Socias i Company

, were included in this study. These selections were grafted onto the peach [ Prunus persica (L.) Batsch] × almond hybrid rootstock ‘Garnem’ and grown in blocks of three trees in an alluvial loamy soil. Nuts were harvested at maturity, when fruit

Free access

D. Esmenjaud, J.C. Minot, R. Voisin, J. Pinochet, and G. Salesses

Resistance variability was evaluated for five rootstock: three Myrobalan plum (Prunus cerasifera Ehr.) genotypes (P.1079, P.2175, and P.2032) grown from in vitro plantlets, one peach (P. persica (L.) Batsch `GF 305') grown from seeds, and one peach-almond hybrid (P. persica × P. amygdalus Batsch `GF 557') grown from rooted cuttings. Twenty-two root-knot nematode populations from different origins were used: Meloidogyne arenaria (Neal) Chitwood (six populations), M. incognita (Kofoid and White) Chitwood (eight populations), M.javanica (Treub) (four populations), M. hispanica Hirschmann (one population), M. hapla Chitwood (two populations), and an unclassified root-knot species (one population). The study was conducted under greenhouse conditions for 1 and 2 months. No galling or nematode reproduction was observed in P.1079 and P.2175, which should be considered immune; P.2032 showed the highest galling and nematode counts when inoculated with M. hispanica and M. javanica. In P.2032, a high proportion of males was recovered in populations that had a limited development. Because the populations of the first four Meloidogyne species reproduce by obligatory mitotic parthenogenesis, high sex ratio maybe the expression of a late form of resistance. Host suitability of `GF 305' was highly variable among M. arenaria and M. incognita populations. A lower relative variation was observed in M. javanica. `GF 557' was resistant to M. arenaria and M. incognita except for one population of M. arenaria that was weakly aggressive and susceptible to M. javanica. Consequently, resistances specific to the genus Meloidogyne for the Myrobalan plum genotypes P.1079 and P.2175, specific to the nematode species for `GF 557', and specific to the nematode population for `GF 305', were evidenced. This study indicates that, in rootstock selection procedures, it is important to test resistance to several populations within the same nematode species.