Light quality of continuous illuminating at night to induce floral initiation of Fragaria chiloensis L. CHI-24-1

A wild strawberry strain, Fragaria chiloensis CHI-24-1, produced inflorescences from both parent and asexually propagated daughter plants linked with runners when grown at 23 °C/20 °C (day/night) under a 24 h day-length (DL) of daylight plus nightly lighting by an incandescent lamp, but not under 8 or 16 h DLs. In the present study, the effect of light quality for continuous illuminating at night on floral initiation of CHI-24-1 plants grown under a 24 h DL was examined. The CHI-24-1 plants were grown under a 24 h DL consisting of natural daylight and continuous lighting at night by an incandescent, a blue fluorescent, a red fluorescent or a far-red fluorescent lamp for 40 days in summer and autumn. Also, the CHI-24-1 plants were grown for 40 days in a growth chamber at 25 °C/20 °C (day/night) with natural daylight and continuous lighting at night by red- and four types of far-red light-emitting-diodes (LEDs with peak wavelengths of 660, 700, 735, 780 and 830 nm). In both experiments, floral initiation of the parent and daughter plants was observed under a stereomicroscope. Although more than 50% of the parent and daughter plants initiated flower buds under the incandescent and far-red fluorescent lamps, about 15% and 0% of those initiated flower buds under blue and red fluorescent lamps, respectively. Floral initiation of the parent and daughter plants occurred under the far-red LED light source whose peak wavelength was 735 nm, but not under the red or the other far-red LEDs. From these results, it can be concluded that the effective light wavelength range of nightly continuous illuminating for floral induction in the CHI-24-1 plants is 735 nm in the far-red light region. Hence, the induction of floral initiation by nightly continuous far-red light (735 nm) appeared to be a response mediated by phytochrome.     

Identification of Petunia hybrida cultivars that diurnally emit floral fragrances

In order to identify genetic resources for breeding fragrant petunias for use as bedding plants, volatile compounds released by day from the flowers of 40 commercial Petunia hybrida cultivars were analyzed using a solid-phase micro-extraction technique coupled with GC–MS. The three cultivars with solid deep-blue flowers that accumulate malvidin in corollas with high tissue pH were found to emit abundant iso-eugenol as the principal floral fragrance. Several other cultivars that emitted considerable amounts of methylbenzoate and/or benzylbenzoate from the flower were also identified. Association between the floral fragrance and the other floral traits such as floral anthocyanin composition and corolla-tissue pH was discussed.     

Reproductive organography of Bougainvillea spectabilis Willd

Bougainvillea spectabilis Willd. is of prime importance for horticulture, as well as potentially for pharmaceutical industries, agriculture and environmental industries. However, its floral development is not yet well understood. A detailed study on floral structure and floral organography in the species was first completed using microscopy of paraffin microtome sections of buds. The results were indicated as follows: first, the three trumped flowers in the cymose inflorescence develop asynchronously. Secondly, Varieties with multi-whorl bracts do not develop any sexual organs, i.e., perianth, pistil and stamens. Thirdly, the wall of the two-loculus anther consists of two kinds of cells: the inner wall, consisting of thick-cytoplasmed cells and the outer wall, consisting of fibrous cells. Fourthly, the pollen grains, with three germination colpi, vary substantially in the form and size in summer under the highest day temperature of 40 °C. Fifthly, the pistil is characterized with betalain-acumulating stylar brush. Followed the developmental course, only one basal ovule is developed in the superior ovary. Finally, organs of one flower develop consecutively from the outer to the inner, i.e., from bracts, to calyx, stamen, and carpel while the three flowers bloomed one by one in one cymose inflorescence. It almost takes 1 week from first bud to the third flower blooming. Our research showed a series of special characteristics of reproduction organography of B. spectabilis which can be useful for understanding its reproduction biology and its sterility.     

Light quality affects in vitro adventitious rooting and ex vitro performance of cherry rootstock Colt

The effect of light quality on in vitro rooting of cherry rootstock “Colt” was studied to evaluate adventitious root development, ex vitro acclimatization and plant growth performance. Adventitious rooting was dependent on the light quality to which the microcutting were exposed. Highest number of roots per microcuttings was recorded under dichromatic light (blue + red). This response could be ascribed to the control of a strong synergistic interaction between phytochromes and blue light photoreceptors. Red light was more effective on root elongation than blue light. In this response a strong synergistic interaction between phytochromes and blue light photoreceptors was suggested. The effect of light quality on the number of root/explant affected the plant during acclimation, scoring the highest level of plant survival in the blue-, red- and blue + red-exposed plantlets. The light quality effect was also observed under greenhouse culture conditions, as shown by growth parameters at the end of six months in plants growth. No specific role was observed for the photoequilibrium of phytochrome. The results reported in this work show that plantlets exposed to different light quality, during the in vitro rooting phase, retain the light quality effects in the subsequent plant acclimatization and greenhouse plant growth phase.     

Early flower initiation allows ample manipulation of flowering time in cherimoya (Annona cherimola Mill.)

Flower initiation date and readiness to flowering in buds of different age were studied in ‘Fino de Jete’ cherimoya (Annona cherimola) cultivar in order to establish the limits for the manipulation of its flowering date. Flower initiation was analyzed by light and scanning electron microscopy (SEM) collecting axillary buds from May to the following February, whereas the bud readiness to produce perfect flowers was determined by forcing buds of different age to sprout by means of leaf removal and tipping the new growth. SEM images confirm that cherimoya buds are differentiated into flowers almost a year before blooming. In this regard, axillary buds have already formed the sepals when the subtending leaf has just begun unfolding (week 0), while the petals are clearly visible in 1-week-old buds. Sectioning of paraffin-embedded buds illustrate that cherimoya buds are in fact a bud complex that 1 week after its inception comprises 4–5 buds of different size of which the two largest ones are reproductive, while the 2–3 smallest buds often remain undifferentiated at that time. The high capacity of flowering expressed by young buds that have been forced to grow proves that cherimoya meristems are early competent for flowering. No differences in fertility or in the time needed to reach anthesis after leaf removal were found among buds of different ages. Node position had no effect on bud break and flowering potential. The early flower initiation in cherimoya deduced from this work opens a wide temporal window for the experimental manipulation of flowering and harvest dates in this crop.     

Photoperiodic reaction of sexual and asexual reproduction in Fragaria chiloensis L. CHI-24-1 plants grown at various temperatures

Floral initiation of a wild strawberry strain, Fragaria chiloensis CHI-24-1, is strongly induced by a 24 h day-length (DL) treatment for 40 days consisting of natural daylight and continuous lighting at night by an incandescent lamp. To use the characteristics of floral initiation in CHI-24-1 as a genetic resource for breeding of cultivated strawberries, the photoperiodic reactions of sexual and asexual reproductive growth under various temperature conditions should be clarified. For that purpose, we examined: (1) floral initiation, inflorescence emergence and runner production seasons of CHI-24-1 plants grown under natural climatic conditions in an open field at the Faculty of Agriculture, Kagawa University and (2) the effects of various DLs and temperatures on floral initiation and runner production of CHI-24-1 plants. When the CHI-24-1 plants were grown under natural conditions, the floral initiation, inflorescence emergence and runner production were observed, respectively, in late autumn, spring, and from spring to autumn. Floral initiation of CHI-24-1 plants was induced strongly by 24 h DL at mean temperatures greater than 20 °C. The maximum floral initiation rates were 90% in the parent plant and 94% in the daughter plants, which were linked by runners to the parent plant. The floral initiation of the daughter plants occurred under 20, 22, and 23 h DL at mean temperatures greater than 20 °C, but not for the parent plants. Floral initiation was induced in 100% of the parent plants by the 8 h DL and the lowest mean-temperature conditions. Results of those experiments indicated that CHI-24-1 was an absolute long day plant having critical DL of about 20 h at mean temperatures greater than 20 °C, even though it was a June-bearing strawberry plant. In addition, CHI-24-1 was a facultative short-day plant at mean temperatures of less than 15 °C.     

Comparison of floral ontogeny in wild-type and double-flowered phenotypes of Syringa vulgaris L. (Oleaceae)

A comparative study of floral ontogeny in normal and double-flowered phenotype of Syringa vulgaris was conducted using the epi-illumination light microscopy. In the wild phenotype, floral differentiation starts with calyx inception and the formation of four sepals in orthogonal positions (two median and two lateral). The corolla emerges as a continuous ring-like structure leading to the appearance of four petal lobes alternating with the sepals. Androecium was formed by initiation of two stamen primordia in transverse plane and finally the bicarpellate gynoecium emerges in median position. In the case of the double-flowered lilac, there are supernumerary petals in an additional whorl. In double-flowered phenotype, a ring meristem is formed acropetally after the first petal whorl initiates. Stamens and carpels initiated similarly in double-flowered as well as in wild-type plants. However, position of stamens deviates from the typical transverse situation. It seems that the appearing of an extra petal whorl did not exhibit any adverse effect on the initiation of other whorls, in terms of organ identity. Therefore, it would be suggested that the double-flowered phenotype of Syringa represents a case of neoheterotopy, with formation of an extra petal whorl, rather than a case of homoheterotopy with transformation of an ancestral androecium whorl into petals.     

Effect of Glomus mosseae and Entrophospora colombiana on plant growth,production, and fruit quality of ‘Maradol’ papaya (Carica papaya L.)

The effect of inoculating ‘Maradol’ papaya plants with arbuscular mycorrhizal fungi (AMF) Glomus mosseae (GM) and Entrophospora colombiana (EC) was assessed. The results showed that both mycorrhizae species increased the number of fruits and yield in papaya plants by 41.9 and 105.2% for GM and 22.1 and 44.1% for EC, respectively, with respect to control plants. GM significantly increased plant height. Sugar content, firmness, color (°Hue), and ripening process of mycorrhized plant fruits were similar to those of the control. Weight loss of mycorrhized plant fruits was considerably less than that of the control. Inoculation of papaya with AMF is recommended, particularly with GM since it increases yield, and fruit weight (45.1%), furthermore, it reduced fruit weight loss during ripening.     

Pome fruit viruses at the Canadian Clonal Genebank and molecular characterization of Apple chlorotic leaf spot virus isolates

A survey for apple and pear viruses was carried out at the Canadian Clonal Genebank (CCG), Harrow, Ontario, Canada, during the fall/winter of 2007 and spring of 2008. Leaves and/or dormant cuttings were randomly collected from 438 to 122 accessions of apple and pear, respectively. Samples were tested by Double Antibody Sandwich-Enzyme Linked Immunosorbent Assay (DAS-ELISA) for the presence of Apple chlorotic leaf spot virus (ACLSV), Apple stem pitting virus (ASPV), Apple stem grooving virus (ASGV) and Apple mosaic virus (ApMV). Infection rates for apples were ACLSV (48.1%), ASGV (10%), ASPV (6.6%) and ApMV (7.1%), and for pears ACLSV (42.6%). ACLSV was detected and characterization by multiplex RT-PCR with primers targeting a fragment of 677 bp corresponding to the partial coat protein (CP), movement protein (MP) and untranslated (3′UTR) region in 22 accessions of apple and pear. Multiplex RT-PCR showed a higher sensitivity over the ELISA test. The nucleotide and amino acid deduced partial CP identities ranged from 82.6–100% to 91–100%, respectively, while partial MP identities was 62.5–100% at aa level based on the amplified fragment appropriate for partial MP using a frame shift, among 22 ACLSV isolates. Phylogenetic analyses based on the partial CP region clustered CCG ACLSV isolates in two different groups, while those based on the partial MP region embraced CCG ACLSV isolates in two sub-clusters within the same group. This is the first report on the detection of ACLSV, ASPV, ASGV and ApMV at CCG, and the molecular characterization of ACLSV isolates in apple and pear plants from worldwide countries to deduce possible heterogeneity and evolution.     

The insertion of the Agrobacterium rhizogenes rolC gene in tomato (Solanum lycopersicum L.) affects plant architecture and endogenous auxin and abscisic acid levels

In the present paper we report on the effects of the insertion of the Agrobacterium rhizogenes rolC gene in the tomato (Solanum lycopersicum L., formerly Lycopersicon esculentum Mill.) cultivar Tondino. Several transgenic lines were successfully obtained, between which two clones, rolC1 and rolC3, were chosen for the analysis of morpho-productive traits as well as of the endogenous levels of auxin and abscisic acid. Consistent with the known phenotypic effect of this gene, the transformed tomato plants were significantly shorter than the corresponding controls. On the other hand, even if yield was not affected by the transformation in terms of average number of fruits produced, fruit weight was significantly lower in the transgenics with respect to the controls. Therefore, insertion of the rolC gene does not lead to an improvement in plant productivity.     

Moving lamps increase leaf photosynthetic capacity but not the growth of potted gerbera

To investigate the responses of leaf photosynthesis and plant growth to a moving lighting system, potted gerberas (Gerbera jamesonii H. Bolus ex J.D. Hook “Festival”) were grown under supplemental lighting in a greenhouse with either a stationary or a moving lighting system positioned above the benches. The stationary system consisted of a fixed high pressure sodium (HPS) lighting system, while the moving lighting system consisted of a moving HPS fixture attached to a cable system to move the light fixture back and forth over the crop. In both cases, the supplemental lighting was applied from 6:00 to 24:00 h with the same supplemental daily light integral (4.9 mol m⁻² day⁻¹). Moving lamps significantly increased leaf photosynthetic capacity as represented by light saturated net CO₂ exchange rate (NCER) (A_sat), light- and CO₂-saturated rate of NCER (A_max), maximum rate of Rubisco carboxylation (V_cmax), maximum rate of electron transport (J_max) and rate of triose phosphate utilization. However, in situ leaf NCER and stomatal conductance, leaf chlorophyll content index, leaf area, leaf thickness, fresh weight of plants were significantly lower under moving lighting than under stationary lighting. It is suggested that the reduced growth of plants under moving lighting might be due to (1) the overall lower light use efficiency of leaves under moving lighting than those under stationary lighting; (2) the slower response time of the photosynthetic system compared to the rate of change in light intensity under moving lighting.     

Establishment of efficient regeneration protocol from leaf explants of Iris pumila shoots cultured in vitro

An efficient plant regeneration protocol via somatic embyogenesis by leaf base culture of in vitro grown Iris pumila shoots was developed. Induction of embryogenic calli was achieved on MS media supplemented with 2,4-dichlorophenoxyacetic acid (2,4-D), kinetin (4.5 μM, each) and some additives (L-proline, casein hydrolysate, adenine sulphate and tyrosine). Further differentiation of embryogenic calli was achieved on MS hormone-free media, and on media supplemented with either BAP (4.5 μM) or BAP + zeatin (4.5 and 0.2 μM, respectively), which allowed somatic embryos, as well as shoot-like structures to form. Fully developed somatic embryos germinated on an MS hormone-free medium. An anatomical study confirmed that shoot-like structures represented early germinating stages of somatic embryos. Acclimatization of plants derived from somatic embryos was 64% after 1 year and no morphological variation was observed.     

Effect of shade regime on flower development,yield and quality in lisianthus

The effects of shading on lisianthus (Eustoma grandiflorum) floral transition, plant development, flower yield and quality, and content of starch and soluble sugars were assessed in three cultivars, over two consecutive years. Shading nets affording 67% or 88% reduction in light intensity, were fitted at planting in the greenhouse for periods ranging from 3 to 8 weeks. Meristem morphology at floral transition was characterized by apical meristem widening and the appearance of two bract primordia. Floral transition time was affected by cultivars, but in general, longer and heavier shade treatments delayed floral transition; the longest delay (6 weeks) being recorded in Mariachi White under 88% shade for 7 weeks or under a combined shade treatment of 88% for 3 weeks followed by 67% for 5 weeks. Despite interactions between cultivar and shade treatment, consistent trends were discerned: the heaviest and most prolonged shading reduced yield (up to 40%), cut stem length (up to 15%), and number of flower buds/stem (up to 26%), within cultivar. Total carbohydrates levels were very low, and it is questionable whether changes observed in carbohydrate quantity following shade treatments had any effect on plant growth or flower yield. Rather, it appears that lisianthus is very dependent on current photosynthesis, so that even a brief shading interlude could reduce branching and flower quality. It may be concluded that the intensive shading usually applied is detrimental for lisianthus.     

Regeneration and characterization of plants derived from leaf in vitro culture of two sweet orange (Citrus sinensis (L.) Osbeck) cultivars

In the current work attempts were made to investigate culture of leaf explants derived from in vitro seedlings of two sweet orange (Citrus sinensis (L.) Osbeck) cultivars, Bingtangcheng and Valencia. Effects of several factors, including culture medium, lighting condition, explant age and genotype on regeneration response were examined based on three parameters, percentage of explants producing shoots, mean number of shoots per explant and shoot forming capacity. Culture of the explants on shoot-inducing media (SIM) composed of MT salts supplemented with different growth regulators gave rise to disparate shoot regeneration, in which SIM₁ (MT + 0.5 mg L⁻¹ BA + 0.5 mg L⁻¹ Kinetin + 0.1 mg L⁻¹ NAA + 3% sucrose + 0.8% agar, pH 5.8) was shown to be the most effective medium for direct induction of shoots from leaf explants. Highly significant difference in the response of shoot bud regeneration was noted between the two cultivars, with Bingtangcheng being more responsive than Valencia. Culture of explants from fully developed leaves led to better shoot regeneration capacity in comparison to undeveloped ones. However, the two lighting conditions used herein did not cause significant difference in shoot regeneration. Phenotypic observation and randomly amplified polymorphic DNA (RAPD) analysis confirmed that all the regenerated plants from both genotypes were genetically identical to their donor plants, suggesting absence of detectable genetic variation in the regenerated plants. The data presented here demonstrated that direct initiation of plants from leaf explants has been successfully accomplished. To our knowledge, this is the first report on direct regeneration of shoots from leaf explants in Citrus, which will provide an alternative source for citrus genetic manipulation in the future.     

African spider flower (Cleome gynandra L./Gynandropsis gynandra (L.) Briq.) as a red spider mite (Tetranychus urticae Koch) repellent in cut-flower rose (Rosa hybrida L.) cultivation

Companion planting of Cleome gynandra, of Kenyan origin, in beds of cut-flower roses reduces significantly red spider mite (Tetranychus urticae Koch) infestation without any detrimental effect on productivity or flower quality. The level of reduction is dependent upon the density of the C. gynandra plants with 15 plants in a 1.8 m² bed (8.3 plants m²) being the most effective, planted either around the bed perimeter or within the rows of roses. The relatively high density of C. gynandra plants required may limit the direct application of this technology in export-focused, greenhouse rose production yet may be of significant value as a supplement to other mite-control strategies. The potential benefits of such companion planting for growers of field roses and those involved in some domestic markets are also evident. Research into the nature and extraction of the active, volatile mite-repellant components of C. gynandra is indicated.     

Both anti-oxidation and lipid-carbohydrate conversion enhancements are involved in priming-improved emergence of Echinacea purpurea seeds that differ in size

This study evaluated the effects of priming on emergence responses of purple coneflower (Echinacea purpurea L. Moench) seeds. The seeds that differ in seed size were either primed with moistened vermiculite (solid matrix priming) or primed in non-aerated −0.5 MPa polyethylene glycol 6000 solution at 25 °C for 6 days (osmopriming), followed by air-drying to their initial moisture level. The tetrazolium staining tests indicated that both large and small seeds were biochemically viable. No notable difference in germination percentage was found between large and small seeds. However, extensive cavity was visible in portions of small seeds in comparison with large seeds. Large seeds accumulated more antioxidants and had greater activities of anti-oxidative enzymes than small seeds. They also had greater isocitrate lyase and malate synthase activities than small seeds. As a result, large seeds had higher emergence percentage and faster emergence speed as compared to that of small seeds. Both solid matrix priming and osmopriming increased emergence percentage and shortened mean emergence time of purple coneflower seeds by increasing the activities of anti-oxidative enzymes and decreasing the levels of malondialdehyde and total peroxide accumulation. Moreover, priming also enhanced the anti-oxidative activities of treated seeds. The activities of isocitrate lyase and malate synthase were also increased in primed seeds. The enhanced anti-oxidation and lipid-carbohydrate conversion activities might explain in part why primed purple coneflower seeds emerged better than non-primed seeds.     

Characterization of antioxidant compounds in Eriobotrya fragrans Champ leaf

Both loquat (Eriobotrya fragrans Champ) fruits and leaves are often used as important ingredients in Chinese herbal formulations for medicinal treatments against cough and asthma, but little information is available about the inherent bioactive chemicals. In this study, 11 major compounds were identified from the acetic ether extract of leaves of the fragrance flower loquat. These chemicals are (1) 2α,19α-dihydroxy-3-oxo-urs-12-en-28-oic acid, (2) 2α-hydroxyursolic acid, (3) ursolic acid, (4) 2α-hydroxyoleanolic acid, (5) tormentic acid, (6) β-daucosterol, (7) epicatechin, (8) cinchonain Ia (9), cinchonain Ib, (10) quercetin-3-O-α-l-rhamnoside and (11) arbutin. Meanwhile, the antioxidant activities of these compounds were evaluated by the DPPH and FRAP assays. Cinchonain Ib exhibited the highest antioxidant activity, followed by cinchonain Ia, epicatechin, quercetin-3-O-α-l-rhamnoside and arbutin.     

Effect of pollination intensity,frequency and pollen source on fig (Ficus carica L.) productivity and fruit quality

Yield and fruit quality in fig (Ficus carica L.) are highly dependent on cultural practices especially caprification (pollination). However, this technique remains not well controlled in Tunisia. This study was conducted during two successive years, 2009 and 2010, to investigate different pollination conditions, i.e. number of caprifigs and repetitions of caprification on fruiting of two cultivars Bouhouli (San Pedro type) and Zidi (Smyrna type). In addition, the efficiency of four pollen sources was evaluated to identify the most effective pollinator for female cultivar Zidi. The following parameters were recorded: fruit number per shoot, fruit set, productivity, fruit characteristics and vegetative growth.     

Identification of seven haplotype-specific SFBs in European pear (Pyrus communis) and their use as molecular markers

The European pear (Pyrus communis) carries the S-RNase-mediated gametophytic self-incompatibility (GSI) system. The S-haplotype is conferred by an S-locus, which contains the style-specific expressed S-RNase, and the pollen-specific expressed F-box genes (SFB). Both the S-RNase and the SFB genes are multi-allelic and each is characteristic of one of the S-haplotypes. Therefore, they are ideal markers for molecular S-genotyping. In this work, for the first time, seven haplotype-specific SFBs were isolated from European pears. Particular primers for each of these SFBs were generated, thus providing an additional tool for S-genotyping of European pear cultivars.