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Comparative analysis of sour cherry cultivars on their ecological and biological indicators
7-28.Views:361Sour cherries developed in the northern hemisphere, an alloploid hybrid of dwarf sour cherries (Prunus fruticosa) and bird cherries (P. avium), born in the confluence of the two species. However, the ecological and, above all, cold tolerance of the ancestor of cultivated sour cherries is higher than that of wild cherries (De Candolle, 1894; Rehder, 1954; Terpó, 1974; Iezzoni et al., 1991; Faust & Surányi, 1997). The cultivation limits are in the northern hemisphere 38-44. degree. The Carpathian Basin, the Balkans and Asia Minor are considered to be the main birthplaces for sour cherries. The genetic and morphological diversity of sour cherries is greater than that of the basic species (Iezzoni et al. 1991; Faust & Surányi, 1997). In the study, 472 sour cherry cultivars were compared based on 7 relative ecological indicators and 3 biological values. Compared to other Prunus species, we mostly found less variability in sour cherries - not counting their salt tolerance (SB). The partial similarity between open pollination (OP), frost tolerance (FR) and disease resistance (DR) - partly true in terms of varieties, but also reflected the effects of purposeful breeding and selection. The cultivars together - in comparison, showed balance, but in the highlighting, the differences of the 3 cultivar groups became significant. Indeed, the differences between the species of the former Hungarian cultural flora are clearly different (Surányi, 2004), which is also the case when comparing a large number of apricot (Surányi, 2014), plum (Surányi, 2015) and peach (Surányi, 2020) varieties.
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Comparative analysis of peach and nectarine cultivars based on their ecological and biological indicators
7-26.Views:381Natural conditions other than the ecological conditions of the Chinese gene center (as 34-38° latitude and 600 to 2400 m above sea level), mainly dry subtropical, i.e. Mediterranean effects, facilitated the development of new forms and varieties (Scorza & Okie, 1991; Faust & Timon, 1995). Probably the primary cause of nectarines, this could also be the primary cause of mutations (probably about 2000 years ago) (Roach, 1985; Surányi, 1985). During the long domestication of peaches, its natural occurrence increased, which was greatly enhanced by its ecological and mutational ability and the organoleptical values of its fruit (Hedrick, 1917; Roach, 1985; Scorza & Okie, 1991; Faust et al., 2011). Through the Ellenberg-Borhidi model and its refinement, the author has demonstrated the suitability of peaches in a broad climate zone based on the relative ecological and biological values of 700 varieties. Among the varieties, clone cultivars and hybrids were Hungarian selected and crossed form, because the diverse environmental conditions of the Carpathian Basin and the past and present size of cultivation were representative (Faust & Timon, 1995; Timon, 2000). It can be concluded from the present relative ecological data that the average standard deviation is below 12% for both peach and nectarine varieties, but the relative biological values were very different. Comparison of cultivars or classical (downy) peaches (n = 562) and nectarines (n = 138) in terms of environmental values confirmed the difference in heat demand and salt tolerance of the two groups of varieties. The pictures of the paper also demonstrated the rich diversity of this fruit species, and after analyzing the apricot and plum varieties (Surányi 2014, 2018), the peculiarities of the relative ecological and biological values of peaches were confirmed.
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Floral biology of tree fruit rootstocks
153-161.Views:173The modern nursery industry requires seed sources of a high quality and regular quantity year by year. Besides the seed sources of processed cultivars (Bartlett pear, Shipley, Elberta peach) special seed orchards are planted with selected seed trees producing high quality and genetically determined seed (hybrid seed or inbred lines). Seedlings are still the most common commercial source of rootstocks for stone fruits (almond, apricot, peach, plum, prune and walnut). Although clonal rootstocks are spreading, usage of seedlings is still predominant at stone fruits and nuts. For successful seed production and planning of seed orchard the knowledge on floral biology, flower fertility, pollination, blossom time of trees (selected clone or cultivars) used for seed production is essential. In this field very little systematic research was carried out most of the papers were published in the second half of the 20th century. Our mini review gives an overview on the importance of flower fertility in the mating systems applied in seed orchards, and the research results on floral biology of fruit tree rootstocks propagated by seed (Prunus avium, Prunus mahaleb, Prunus armeniaca, Prunus cerasifera, Prunus insititia, Prunus amygdalus, P persica, P amygdalopersica, Pyrus pyraster, Pyrus communis and Pyrus betulifolia) over the last decades.
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Flower visiting activity of honeybees on fruit species blooming subsequently
12-16.Views:195In the small demonstration orchard of the College Faculty of Horticulture at Kecskemét the blooming time, the flower density and the honeybee activity was observed at a number of cultivars of 20 flower species during four consecutive years.
Fruit crop species were in flower during 3-4 months altogether. The blooming period of them was classified into five groups as early (almond, apricot, gooseberry), middle early (sweet cherry, red currant, currant-gooseberry, black currant, white currant, peach, plum, sour cherry), middle late (pear, strawberry, apple), late (black elder, quince, medlar, raspberry, blackberry-raspberry) and very late blooming period (blackberry). The blooming period of the members of the groups of early and medium early blooming often coincided partly and the same happened between the medium and the medium late as well as between fruits of late and very late flowering.
The flower density of some fruit species is extremely variable (currant-gooseberry, medlar), while at others it is fairly stable and evenly dense in consecutive years (sour cherry, sweet cherry, strawberry). At other fruit species it is moderately changeable. Some fruit species tended to attract more honeybees than others (plum, apple, quince, medlar) and some of them tended to attract much less (black elder, pear) but most species can be regarded as of medium attractivity.
On the flowers of some fruit species (pear, strawberry, quince) honeybees gathered pollen predominantly. At most fruit species however pollen and nectar gathering behaviour seemed to be gradually changing during the season. Namely most honeybees tended to gather pollen at the flowers of the early blooming fruit species, but on the other hand typical foraging behaviour gradually shifted to nectar gathering at the flowers of fruit species of moderate and late blooming periods.
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The effect of the limitation of insect pollination period on the fruit set and yield of temperate-zone fruit tree species
90-95.Views:221The duration of effective bee pollination period was limited by caging flowering branches for shorter or longer time in blooming fruit trees in a number of experiments during the past decades. In the case of self-sterile fruit species and cultivars (apples, pears, quinces, some plums, some sour cherries) even partial limitation of the effective duration of bee pollination period significantly reduced the fruit set and the yield. In the case of self-fertile apricots the effect of the total and also the influence of partial limitation of bee pollination period was the same as in the case of the mentioned self-sterile fruits. On the other hand, in the case of another self-fertile fruits (some plums, some sour cherries), the effect of partial limitation of bee pollination period was usually small, but complete (or incomplete but strong) limitation of be pollination usually resulted in a strong reduction of yield. This means that not only self-sterile but also self-fertile fruits clearly depend on insect (bee) pollination. This is because pollen dehiscence of anthers and the receptive period of stigmas do not overlap in time within the individual flowers. Stigmas in self-fertile trees, therefore, need pollen carried by bees from another flowers of the same tree (or compatible pollen from another trees). Accordingly, additional bee pollination (moving bee colonies to the orchards in flower) is needed to all kinds of temperate-zone fruit tree species when bee visitation of plantations is not abundant enough for some reasons.
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Pollen morphology of fruit species
49-57.Views:1206Size and surface morphology of pollen has been studied in 87 twit varieties of 10 fruit species during the period of 1990-1995. No preceding work of that type came to our knowledge, yet.
The samples comprised a wide variety of cultivars included male sterile, self-incompatible, partially self-fertile stone fruits, diploid and hexaploid plums, diploid and triploid apples.
The large number of species and varieties facilitated the comparison of items within and between the respective species.
It was stated that the size, shape and surface morphology of pollen is genetically determined and those data, combined with other variety characters, are suitable for the classification and distinction of varieties.
In assessment of pollen size and shape, their moisture content is crucial. The major diameter of the swollen pollen as well as the length and width of the dry grains are characteristic to species and/or to variety.
The width and shape changes largely with moisture content. Large grains are proper to quince, apricot, peach and almond, medium sizes are found in apple, sweet cherry, sour cherry, European plum, whereas small size is typical to Japanese plums.
The low number of varieties studied does not allow conclusions concerning differences within pears, quinces and almonds as species. In the rest of species, valid differences have been registered as between varieties.
Within species, as apple and plum, the effect of ploidy (i.e. number of chromosomes) was expressed in the size of their pollen. In stone fruit species, the correlation between size. of anthers and size of pollen grains was positive.
Genetic relations between the self-fertile sour cherry varieties of the Pándy type (Debreceni bőtermő, Kántorjánosi, Újfehértói fürtös) as well as the self-incompatible apricots of "giant" fruit size are supposed to be analysed by pollen studies but there did not turn out any decisive conclusion, yet. Other characters also should be considered.
The assembly of pollen characters is decisive in the determination of the variety. The ratio of empty pollen grains, the grain size and the density as well as the size of the pits on the surface are best suited to distinguish pollen lots.