Review of recent advances in post-harvest techniques for tropical cut flowers and future prospects: Heliconia as a case-study.

Aesthetic attributes and easy-to-grow nature of tropical cut flowers (TCFs) have contributedto their potential for increased production. The dearth of information regarding agronomic practices and lack of planting materials are the key hindrances against their fast expansion. Unconventional high-temperature storage requirements and the anatomy of the peduncle contribute topoor vase life performance, while troublesome packaging and transport due to unusual size and structureprimarily cause post-harvest quality deterioration. Nonetheless, the exotic floral structuresconsequently increase market demand, particularly in temperate countries. This boosts studies aimed at overcoming post-harvest hindrances. While a few TCFs (Anthurium, Strelitzia, Alpinia, and a few orchids) are under the spotlight, many others remain behind the veil. Heliconia, an emerging specialty TCF (False Bird-of-Paradise, family Heliconiaceae), is one of them. The structural uniquenessand dazzling hues of Heliconia genotypes facilitate shifting its position from the back to the forefrontof the world floriculture trade. The unsatisfactory state-of-the-art of Heliconia research and the absence of any review exclusively on it are the key impetus for structuring this review. In addition to the aforementioned setbacks, impaired water uptake capacity after harvest, high chilling sensitivity, and the proneness of xylem ducts to microbial occlusion may be counted as a few additional factors that hinder its commercialization. This review demonstrates the state-of-the-art of post-harvest research while also conceptualizing the implementation of advanced biotechnological aid to alleviate the challenges, primarily focusing on Heliconia (the model crop here) along with some relevant literature on its other allied members. Standard harvesting indices, grading, and packaging are also part of the entire post-harvest operational chain, but since these phases are barely considered in Heliconia and the majority of tropical ornamentals except a few, a comprehensive account of these aspects has also been given. The hypothesized cues to nip chilling injury, resorting to different bio-chemical treatments, nano-based technology, and advanced packaging techniques, may help overcome preservation difficulties and propel its transition from niche to the commercial flower market. In a nutshell, readers will gain a comprehensive overview of how optimum post-harvest handling practices can rewardingly characterize this unique group of TCFs as the most remunerative component.

Molecular cloning and potential function prediction of homologous SOC1 genes in tree peony.

KEY MESSAGE: The central flower integrator PsSOC1 was isolated and its expression profiles were analyzed; then the potential function of PsSOC1 in tree peony was postulated. The six flowering genes PrSOC1, PdSOC1, PsSOC1, PsSOC1-1, PsSOC1-2, and PsSOC1-3 were isolated from Paeonia rockii, Paeonia delavayi, and Paeonia suffruticosa, respectively. Sequence comparison analysis showed that the six genes were highly conserved and shared 99.41% nucleotide identity. Further investigation suggested PsSOC1 was highly homologous to the floral integrators, SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1), from Arabidopsis. Phylogenetic analysis showed that the SOC1 protein clustering has family specificity and PsSOC1 has a close relationship with homologous SOC1 from Asteraceae species. The studies of PsSOC1's expression patterns in different buds and flower buds, and vegetative organs indicated that PsSOC1 could express in both vegetative and reproductive organs. While the expression of PsSOC1 in different developmental stages of buds was different; high expression levels of PsSOC1 occurred in the bud at the bud sprouting stage and the type I aborted the flower bud. PsSOC1 expression was also shown to be affected by gibberellins (GA), low temperature, and photoperiod. One of the pathways that regulates tree peony flowering may be the GA-inductive pathway. Ectopic expression of PsSOC1 in tobacco demonstrated that greater PsSOC1 expression in the transgenic tobacco plants not only promoted plant growth, but also advanced the flowering time. Finally, the potential function of PsSOC1 in tree peony was postulated.

Endogenous isoflavone methylation correlates with the in vitro rooting phases of Spartium junceum L. (Leguminosae).

Spartium junceum L. (Leguminosae) is a perennial shrub, native to the Mediterranean region in southern Europe, widespread in all the Italian regions and, as a leguminous species, it has a high isoflavone content. An in vitro culture protocol was developed for this species starting from stem nodal sections of in vivo plants, and isoflavone components of the in vitro cultured tissues were studied by means of High Performance Liquid Chromatography (HPLC) analytical techniques. Two main isoflavones were detected in the S. junceum tissues during the in vitro propagation phases: Genistein (4',5,7-Trihydroxyisoflavone), already reported in this species, and its methylated form 4',5,7-Trimethoxyisoflavone, detected for the first time in this plant species (0.750 ± 0.02 mg g(-1) dry tissue). The presence of both of these compounds in S. junceum tissues was consistently detected during the in vitro multiplication phase. The absence of the methylated form within plant tissues in the early phases of the in vitro adventitious root formation was correlated with its negative effect displayed on root induction and initiation phases, while its presence in the final "root manifestation" phase influenced positively the rooting process. The unmethylated form, although detectable in tissues in the precocious rooting phases, was no longer present in the final rooting phase. Its effect on rooting, however, proved always to be beneficial.

Micropropagation of Helleborus through axillary budding.

Helleborus genus, belonging to the Ranunculaceae family, has 20 species of herbaceous perennial flowering plants. The commercial exploitation of this plant is dependent on the selection and propagation of appropriate lines. High propagation rate could be accomplished by using a suitable tissue culture method enabling the rapid introduction of valuable selections in the market. However, in vitro cultivation of Helleborus is still very difficult. Thereby the development of reliable in vitro propagation procedures is crucial for future production systems. Axillary buds cultured on agar-solidified Murashige and Skoog medium supplemented with 1 mg/L benzyladenine, 0.1 mg/L ß-naphthoxyacetic acid, and 2 mg/L isopentenyl adenine develop shoots after 16 weeks of culture under 16 h light regime, 50-60 µmol/s/m(2), and 19 ± 1°C. The multiplication rate ranges from 1.4 to 2.1. However, the genotype and the number of subcultures affect the efficiency of the micropropagation process. The rooting of shoots is about 80% in solidified MS medium containing 1 mg/L 1-naphthaleneacetic acid and 3 mg/L indole-3-butyric acid. The described protocol provides information which can contribute to the commercial production of Helleborus plants.

In vitro propagation through axillary shoot culture of Ranunculus asiaticus L.

Ranunculus asiaticus is an important ornamental species mainly cultivated in the countries surrounding the Mediterranean sea. So far, the multiplication of this plant has been mainly carried out by seed and tuberous root division; however, these systems present many drawbacks. Tissue culture is an attractive alternative for accelerated propagation of selected and indexed genotypes. In this chapter, we present a flow chart for the commercial production of Ranunculus clones by using in vitro axillary budding. Although the price of micropropagated plants is higher compared to traditional material (seedlings and tuberous roots from seed populations), we need to consider that micropropagation helps to supply growers with more performant and healthy genotypes, and a better production schedule can be envisaged for cultivation and packaging.