The study of ovule senescence in the ovaries of four sweet cherry cultivars (‘Karina᾿, ‘Kordia᾿, ‘Regina᾿ and ‘Summit᾿) in the environmental conditions of West Serbia was carried out. Monitoring of ovaries was performed using the fluorescence microscopy method, on emasculated and pollinated flowers (cross-pollination variant), non-emasculated open-pollinated flowers (open pollination variant), and emasculated unpollinated flowers (unpollinated variant). In cross- and open pollination variants, the rate of unusual pollen tube growth in the ovary, fertilization percentage and fruit set were determined. The tendency in the appearance of fluorescence, as an indicator of ovule senescence, showed strong genotypic dependence ‒ it was the most and the least pronounced in the ovaries of ‘Kordia’ and ‘Regina’, respectively, in all the flower categories. Investigation of unusual pollen tube growth, fertilization percentage and fruit set, considered from the aspect of ovule senescence and cultivars’ behaviour as female (pollinated), pointed to their specific relations and complex dependence on the air temperature before and during the flowering. Flower emasculation and pollination also influenced ovule senescence, and this impact was unequal by genotypes, i.e. those having better ovule vitality in general, had also better ovule vitality in the conditions of emasculation, and pollination absence. The results imply different adaptation of cultivars to higher temperatures before and during the flowering, pointing to the further investigation related to the good adaptability of genotypes to air temperatures in reproductive sense, which is a basic indicator of good adaptability in general.

A study was conducted to investigate the effect of different storage periods and temperatures on pollen viability in vitro and in vivo in plum genotypes ‘Valerija’, ‘Čačanska Lepotica’ and ‘Valjevka’. In vitro pollen viability was tested at day 0 (fresh dry pollen) and after 3, 6, 9 and 12 months of storage at four different temperatures (4, −20, −80 and −196 °C), and in vivo after 12 months of storage at distinct temperatures. In vitro germination and fluorescein diacetate (FDA) staining methods were used to test pollen viability, while aniline blue staining was used for observing in vivo pollen tube growth. Fresh pollen germination and viability ranged from 42.35 to 63.79% (‘Valjevka’ and ‘Čačanska Lepotica’, respectively) and 54.58 to 62.15%, (‘Valjevka’ and ‘Valerija’, respectively). With storage at 4 °C, pollen viability and germination decreased over the period, with the lowest value after 12 months of storage. Pollen germination and viability for the other storage temperatures (−20, −80 and −196 °C) were higher than 30% by the end of the 12 months. Pollination using pollen stored at 4 °C showed that pollen tube growth mostly ended in the lower part of the style. With the other storage temperatures, pollen tube growth was similar, ranging between 50 and 100% of the pistils with pollen tubes penetrated into the nucellus of the ovule in the genotype ‘Čačanska Lepotica’. The results of these findings will have implications for plum pollen breeding and conservation.