The minirhizotron system gives opportunity to study the root development without disturbing the soil and root. We have found certified differences in root development during the year 2013 among the rootstocks grafted on ‘Cabernet sauvignon’. The number of roots varied according to the rootstocks in different depth of soil layers and also va...ried the development of ripeness of the root system. We conclude that root system development is affected by soil physical and chemical properties, but differences according to the rootstock genotype on the similar type of soil exist.
The aim of this paper was to investigate the fl owering characteristic of apples and their relationship to meteorological parameters. The trees observed are grown at Újfehértó, Eastern Hungary in the plantation of an assortment (gene bank) with 586 apple varieties. Each of the varieties were observed as for their dates of subsequent phenopha...ses, the beginning of bloom, main bloom and the end of bloom over a period between 1984 and 2001 during this period the meteorological data-base keeps the following variables: daily means of temperature (°C), daily maximum temperature (°C), daily minimum temperature (°C), daily precipitation sums (mm), daily sums of sunny hours, daily means of the differences between the day-time and night-time temperatures (°C), average differences between temperatures of successive daily means (°C). Between the 90th and 147th day of the year over the 18 years of observation. The early blooming varieties start blooming at 10–21April. The varieties of intermediate bloom start at the interval 20 April to 3 May, whereas the late blooming group start at 2–10 May. Among the meteorological variables of the former autumnal and hibernal periods, the hibernal maxima were the most active factor infl uencing the start of bloom in the subsequent spring.
The trees observed are grown at Ujfehert6, Eastern Hungary in a gene bank with 555 pear cultivars. Each of the cultivars was monitored for its dates of: the beginning of bloom, main bloom and the end of bloom and ripe phenophasis separately between I 984 and 2002. We analyzed the statistical features, frequency, distribution of these phenophasi...s and its' correlation the meteorological variables bet ween the interval. During this period the meteorological database recorded the following variables: daily mean temperature (°C), daily maximum temperature (0C), daily mini m um temperature (0C), daily precipitation (mm), daily hours of bright sunshine, daily means or the differences between the day-time and night-time temperatures (0C). For the analysis of data the cultivars have been grouped according to dates of maturity, blooming period as well as types of the seasons. Groups of maturity dates: summer ripe, autumnal ripening, winter ripe cultivars. Groups of blooming dates: early blooming, intermediate blooming, late blooming cultivars. At all the separated groups we analyzed the relationship between phenophasis and meteorological variables. During the 18 years of observation , the early blooming cultivars started blooming on 10-21 April, those of intermediate bloom date started flowering bet ween 20 April and 3 May, whereas the late blooming group started on 2- 10 May. Among the meteorological variables of the former autumn and winter periods, the winter maxima were the most active factor influencing the start dates of bloom in the subsequent spring. For the research of fruit growing-weather relationships we used simple, well known statistical methods, correlation and regression analysis. We used the SPSS 1 1.0 software for the linear regression fitting and for calculation of dispersions as well. The 1ables made by Excel programme.
We have concluded the selection tests of the `Mézes körte' seedlings planted in the spring of 2006, with special emphasis on the cotyledonary, foliage leaf and the height of plant. Out of the 75 seeds planted in rows, there were 40-45 pieces growing out, so during the first cotyledonary test we had to calculate with almost 40% decay. On 12th...April 2006, we recorded some of the important characteristics of the seedlings in their cotyledonary stage which characteristics were important from the point of view of selection (cotyledonary form, cotyledonary length, cotyledonary thickness, cotyledonary colour, cotyledonary petiole length, cotyledonary petiole thickness, cotyledonary petiole colour). The above morphological characteristics are shown in Table No. 1-6. We have also tested the seedling in foliage leaf state, paying special attention on the development stage of the plants (colour of foliage leaf , height of plant). We have completed statistical calculations of the two above mentioned characteristics. The result of that is summarised in Table No. 8-9. The variation coefficient show smaller value in the case of the foliage leaf number (15-32%), while the wider range of spread of the data referring to the height of the plant is shown by the 33-61% CV values. On charts No 4-9. we present the relationship between the height of the plant and the number of foliage leaf, as well as the differences between the two graphs. Based on the above charts and graphs it can be defined that the 40% destruction of the developing seedlings during the period till the next measurement reached 70-80% level. In spite of this however some seedlings showed strong and balanced growth (A44, B42, C25, D16, E5, E39, F38), the further testing and selection of those is to be completed in the future.
An assortment of 17 pear varieties was examined in 2006 at Keszthely, Department of Horticulture, Georgicon Faculty of Agriculture, Veszprem University. The selected varieties were planted in 1980, grafted on seedling rootstock and represented the majority of existing pear plantations in Hungary. The main objective was the determination of suit...ability of the most important varieties for the purpose of intensive growing technologies even when grafted on vigorous seedling rootstock. The most important growing and fruiting characteristics of the varieties have been assessed and evaluated from the point of view of productivity. We stated that the relations of the trunk or the main axis to the lateral branches and fruiting structures are all subject to varietal effects and are valuable indices of the growing character. The quotient of the diameters of trunk and branch should be around 0.3-0.4, and the relative frequency of fruiting structures (Dárda, nyárs, vessző) meaning the ability of branching and regeneration associated with accurate pruning policies are decisive from the point of view of promising success.
Detailed studies were made on the nectar production of 44, 16 and 18 pear cultivars, respectively, in a cultivar collection of pear during three consecutive years with highly different weather in the blooming. Results clearly show that pear does not necessarily produce small amount of nectar as stated in the world literature. In fact, pear can...produce extremely high amount of nectar sometimes much higher than other temperate zone fruit trees species but its nectar production is highly subjected to weather, first of all to air temperature. Low nectar production seems to be more frequent than high one and cold weather can prevent its nectar production at all. On the other hand, results corroborate to the earlier statements on the low sugar concentration of pear nectar. There is a highly significant negative correlation between the amount of nectar produced by pear flowers and its sugar concentration (r = -0.52, n = 291, p< 0.001 for 1996, r = -0.34, n = 197, p< 0.001 for 1998). Sugar concentration in individual flowers may be up, to 40% in exceptional cases but generally it is well below 20%. Very high figures for sugar concentration in pear nectar at the literature seem to be incomprehensible. In contrast of some earlier statement in the literature no real difference could be established in the nectar production of pear cultivars, based on much more measurements than in earlier studies. Very low sugar concentration in pear nectar can explain the fact that the overwhelming majority of honeybees are pollen gatherers at pear trees even in the case of exceptionally high nectar production.
The 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.