Vascular occlusion in stems of cut rose flowers exposed to air: Role of xylem anatomy and rates of transpiration

Stems of cut rose flowers were exposed to air at 20°C and 60% relative humidity and then placed in water. The rate of water uptake in Frisco, Sonia, Madelon, and Cara Mia roses was maximally inhibited after 72, 36, 24, and 3 h of exposure to air. respectively. Anatomical observations showed no tyloses, gums, or deposition of hydrophobic material in the xylem conduits (tracheids and vessels) of any of the investigated cultivars. Frisco, Sonia, Madelon, and Cara Mia roses showed no difference in the number, the length, the wall thickness, or the diameter of the lumina of either the tracheids or the vessels. This indicates that differences in recovery are not related to capillary diameter or length.
During exposure to air the decrease in transpiration rate, fresh weight, and water potential was the same in Sonia, Madelon, and Cara Mia roses. Upon exposure to air Frisco roses lost less water than the other cultivars studied In Frisco roses stomatal conductance was similar to that of other cultivars, but the rate of cuticular transpiration was lower.
It is concluded that conservation of water through low cuticular transpiration is one of the reasons for the relatively slow development of the vascular occlusion in Frisco roses, but the differences between Sonia. Madelon and Cara Mia roses were not related to their rates of transpiration.     

Cytokinins in Rosa hybrida in relation to bud break

To assess the role of endogenous cytokinins in growth and development of Rosa hybrida , their concentrations in bleeding sap and in roots, stem, leaves, axillary shoots and bottom breaks in three stages of development were quantified. Cytokinins were purified by means of immunoaffinity chromatography and HPLC, and identified by retention time, UV spectrum and GC-MS. The major translocation form in the xylem was zeatin riboside (ZR). In all mature tissues, cytokinins of the zeatin-type were predominant, amounting to 80–90% of the total cytokinin concentration. The stems contained high concentrations of cytokinins, probably caused by lateral movement of ZR from the xylem to adjacent stem tissue and the ability of the stem to metabolize cytokinins. In young leaves the contribution of isopentenyl adenine (iP)-type cytokinins to the total cytokinin pool was about 50%, indicating that these leaves might be capable of de novo synthesis of cytokinins. In older leaves, the concentration of an unidentified cytokinin-like compound increased to more than 50% of total cytokinins. This compound, which was also found in the roots, might be a storage form of cytokinins. In young axillary shoots, about 50% of the cytokinins are iP-compounds, suggesting either import of iP-type cytokinins via the phloem or de novo synthesis of cytokinins. In buds forming bottom breaks, ZR and zeatin riboside monophosphate (ZRMP) are the main cytokinins, indicating that these buds receive their cytokinins from the roots.     

Physiological response of cut rose flowers to cold storage

The effects of low temperature storage on the physiology of cut rose flowers ( Rosa hybridaL. cv. Mercedes) were studied. Extension of cold storage or increase in temperature (from 3 to 8°C) was accompanied by shortening of vase life and advancement of petal senescence, as reflected in an advance in the timing of the rise in ethylene production and an increase in membrane permeability (ion leakage). Although storage at a relative humidity (RH) of 65% reduced petal water content by 20% in comparison with flowers stored at 95% RH, it did not shorten vase life. The progression of petal senescence was measured during storage at 3°C and during aging at 22°C. Both ethylene production rates and membrane microviscosity measured by fluorescence depolarization increased with time at 3°C and at 22°C, but more slowly at 3°C. At 3°C membrane permeability measured by ion leakage did not increase. Following cold storage the rate of ethylene production in the petals was increased by up to eight times the rate in unstored flowers. Silver thiosulphate extended the vase life of both stored and fresh flowers equally by 2 days, but did not increase the life of stored flowers to that of treated fresh flowers. It is concluded that the primary effect of cold storage on roses is to slow down senescence and that the continued slow senescence leads to shorter vase life. The possible occurrence of sequential processes during senescence and the effects of temperature on these processes is discussed.     

Tumor Transformation of Petunia hybrida via Pollen Co-Cultured with Agrobacterium tumefaciens

Pollen preparations usually show a high nuclease activity. Therefore, to avoid DNA degradation, co-cultures of pollen and Agrobacterium tumefaciens were evaluated as a new tool in gene transfer experiments. As a model system, Petunia pollen was co-cultured with an A. tumefaciens wild strain. The co-cultured pollen was used for pollination of Petunia flowers. The seeds obtained were germinated and one cotyledon per seedling was removed and put stalk upwards on nutrient agar. In 80% of the cotyledons a callus developed from the cut surface of the stalks which was screened for tumor transformation on hormone-free medium. In repeated subculturing some calli maintained growth on hormone-free medium. Two of these calli were habituated. One callus, the best growing one, showed on Southern blot analysis a distinct hybridization signal at 3.2 kb when probed with Hind III fragment 22 DNA, covering two genes responsible for hormone free growth. This is the exact size that could be expected when plant material has been transformed with T-DNA. Another callus gave a hybridization signal at 2 kb which could only be explained with chromosomal rearrangement. In these two calli there was no co-transformation of the nos-gene: nopaline synthase activity could be detected from none of the calli, and none of the calli DNAs hybridized when probed with the nos-gene. Bacterial contamination could be excluded by probing the DNAs with virfragments.     

Nucleus substitution between Petunia species using gamma ray-induced androgenesis

Summary The ovaries of two different Petunia species: Petunia hybrida (hort) and Petunia parodii (Steere) were irradiated with -ray doses ranging from 50 to 1,000 Gy before pollination. Seed setting occurred after 4 days preculture on a non-sterile medium. Ovaries transformed into fruits were then cultivated aseptically with the following results: (1) -ray doses ranging from 200 to 1,000 Gy led to the development of two types of plants: haploids 2n=x=7 and overdiploids 2n>2x=14. (2) The androgenetic origin of haploids was ascertained by using genetic markers. The origin of overdiploids is discussed. (3) Androgenetic haploids contained the chloroplasts of the irradiated female parent. No visible change of cp DNA patterns was observed after irradiation. (4) The four possible androgenetic events were successfully obtained between the two Petunia species: hybrida haploids with hybrida or parodii cytoplasm, and parodii haploids with parodii or hybrida cytoplasm.     

Synthesis of malvidin and petunidin in pigmented tissue cultures ofPetunia hybrida

Summary In petunia cells culturedin vitro anthocyanin synthesis is usually repressed resulting in white/ yellow cells. However, we observed that in petunia strain AK-5000 purple cells appeared at a frequency of about 5 × 10^–5. Analysis of the pigments showed that these cells contained the same anthocyanidins (petunidin and malvidin) as found in corollas of the parental plants. This suggests an induction of anthocyanin synthesis in these cells. In white/yellow cells, from which these pigmented cells originated, we could not observe any of the known precursors of these pigments.     

S-alleles are retained and expressed in a self-compatible cultivar of Petunia hybrida.

Summary We identified two S-allele-associated proteins (S-proteins) in a self-compatible cultivar of Petunia hybrida based on their segregation in F₁ hybrids between P. hybrida and its self-incompatible relative, Petunia inflata (with S₂S₂ genotype), and in selfed progeny of P. hybrida. These two S-proteins, designated S_x-protein (24 kDa) and S_o- protein (31 kDa), are pistil specific, and their expression follows a temporal and spatial pattern similar to that of S-proteins characterized in self-incompatible solanaceous species. Their amino-terminal sequences also share a high degree of similarity with those of solanaceous S-proteins. Selfing of P. hybrida yielded plants with S_oS_o, SxSo, and S_xS_x genotypes in an approximately 1:2:1 ratio, indicating that the S_x- and S_o-alleles, though expressed in the pistil, failed to elicit a self-incompatibility response. The S₂-allele of P. inflata is expressed in all the F₁ hybrids, rendering them capable of rejecting pollen bearing the S₂-allele. The S_o-allele is not functional in the F1 hybrids, because all the F₁ progeny with S₂S_o genotype are self-compatible. However, in F₁ hybrids with S₂S_x genotype, approximately half are self-incompatible and half are self-compatible, indicating that the function of the S_x-allele depends on the genetic background. These results strongly suggest that the presence of functional S-alleles alone is not sufficient for expression of a self-incompatibility phenotype, and reaffirm the multigenic nature of gametophytic self-incompatibility suggested by earlier genetic studies.