Changes in the Activity of Acetyl CoA Carboxylase in Germinating and Ripening Sunflower Seeds

Activity of acetyl CoA carboxylase was determined in germinating and maturing sunflower (Helianthus annuus L.) cv. Rum Sun Record seeds. A constant decrease was observed in germi nating embryos. Exposure of etioplasts to light intensity of 500 (74 mW . cm^?2) lux for different time intervals decreased the activity of the enzyme in the embryos. A reverse trend was observed in ripening embryos where the ATP-Pi exchange rate was found to be directly correlated to the activity of acetyl CoA carboxylase.     

Developing phosphinothricin-resistant transgenic sunflower (Helianthus?annuus L.) plants

Most investigations on genetic transformations of sunflower have used the neomycin transferase (nptII) gene as the selectable marker. We previously reported a PPT-based selection system for sunflower transformation that uses the bialaphos resistance (bar) gene as the selectable marker and 20 mg/l of phosphinothricin (PPT) as the selective agent. Sunflower (Helianthus annuus L.) variety Skorospeliy 87 was genetically transformed via Agrobacterium tumefaciens strain EHA 105 harbouring the binary plasmid vector pBAR. Two-day-old explants from mature embryos competent for direct shooting were used. Southern blot and ELISA experiments confirmed the stability of expression in two generations of transgenic plants. Transformed plants transferred to soil in the greenhouse exhibited resistance to the herbicide Basta^? at 3 l/ha.     

Direct somatic embryogenesis and plant regeneration from immature embryos of hybrid sunflower (Helianthus annuus L.) on a high sucrose-containing medium

Somatic embryos of sunflower (Helianthus annuus) were obtained by placing immature zygotic embryos on a high sucrose (12%) containing medium. The somatic embryos were first observed 6 days after culture and a callus intermediate was not formed. Histological examination revealed the classical stages of embryo development. The somatic embryos proliferated directly from the surface of the zygotic embryos and germinated after placement on a low sucrose medium. Seeds have been obtained from regenerated plants.Abbreviations 2,4-D 2,4-dichlorophenoxyacetic acid - NAA 1-naphthaleneacetic acid - IAA Indole-3-acetic acid - BAP 6-benzylamino purine. Salaries and research support were provided by State and Federal funds appropriated to OSU-OARDC. Journal Article No. 67–87     

ORGANOGENESIS FROM HELIANTHUS ANNUUS INBREDS AND HYBRIDS FROM THE COTYLEDONS OF ZYGOTIC EMBRYOS

Dormant mature and immature zygotic embryos of sunflower (Helianthus annuus L.) inbreds and hybrids were dissected and cultured on modified Murashige and Skoog's medium supplemented with 0.1 mg/l benzyl adenine (BA), 0.5 mg/l naphthalene acetic acid (NAA), adenine sulfate, and casamino acids. For certain inbreds and hybrids, adventitious shoot formation occurred from callused cotyledonary tissue, particularly along the cut edges. The developmental stage of the zygotic embryo was critical. Eighty percent of immature H. annuus ‘Mammoth Russian’ embryos produced adventitious shoots from cotyledons, while mature embryos did not. The organogenic potential of mature cotyledons diminished as soon as one day after germination was initiated. Different forms of regeneration were observed in two inbred lines, and when these were crossed, both forms of regeneration were observed at a lower frequency from the immature embryos of the hybrid. Rooted shoots were successfully grown to maturity in a greenhouse.     

Production of stable transgenic sunflowers (Helianthus annuus L.) from wounded immature embryos by particle bombardment and co-cultivation with Agrobacterium tumefaciens

Split embryonic axes of 21-day old immature sunflower (Helianthus annuus L.) embryos were bombarded by microparticles and then co-cultured with disarmed Agrobacterium tumefaciens strain EHA105 bearing a binary vector carrying nptII and uidA genes. Apical shoot bud development and organogenesis induced on the explants led T₀ transgenic plants. Southern blot analysis revealed complex integration patterns in T₀ plants. The uidA gene segregated as a dominant trait and single-insertion events were observed in T₁ plants. Patterns similar to those of T₁ plants were observed in T₂ progeny.     

Dehydrating immature embryo split apices and rehydrating with<Emphasis Type="Italic">Agrobacterium tumefaciens</Emphasis>: A new method for genetically transforming recalcitrant sunflower

Split embryonic axes of 21-day-old immature sunflower (Helianthus annuus L. var. RHA266) embryos were bombarded, vacuum infiltrated, or dehydrated before being infected byAgrobacterium tumefaciens strain EHA 105, bearing a binary vector carrying the selectable markerNPTII and the scorable markeruidA gene. RHA266 was found to be particularly sensitive to in vitro culture and recalcitrant to organogenesis. Of the 3 methods used, only dehydration and rehydration withAgrobacterium gave rise to transient GUS expression in shoot apices and stably transformed plants as confirmed by Southern blotting analysis.     

Callus induction and plant regeneration from mature embryos of sunflower

Callus development and efficient shoot and root organogenesis were obtained from five different sunflower (Helianthus annuus L.) genotypes: Trakya 80, Trakya 129, Trakya 259, Trakya 2098, and Viniimk 8931, which are commercially important for Turkey. Plant tissue culture systems were established on Murashige and Skoog (MS) media supplemented with various plant growth regulators using mature embryos of sunflower. For callus induction MS + 1 mg/l 2,4-D, for shoot regeneration MS + 1 mg/l benzyladenine and 0.5 mg/l α-naphthaleneacetic acid were used. Callus induction ratios were around 80–92% in all tested genotypes. The Trakya 259 genotype gave the best shoot regeneration response (44%). All regenerated shoots were rooted on MS medium supplemented with 1 mg/l indolyl-3-butyric acid and on MS medium without any hormones. Mature embryos could be an alternative source for indirect plant regeneration and gene transfer systems for different sunflower genotypes. Published in Russian in Fiziologiya Rastenii, 2006, Vol. 53, No. 4, pp. 621–624. The text was submitted by the authors in English.     

Sunflower resistance to multiple downy mildew pathotypes revealed by recognition of conserved effectors of the oomycete Plasmopara halstedii

Over the last 40 years, new sunflower downy mildew isolates (Plasmopara halstedii) have overcome major gene resistances in sunflower, requiring the identification of additional and possibly more durable broad‐spectrum resistances. Here, 354 RXLR effectors defined in silico from our new genomic data were classified in a network of 40 connected components sharing conserved protein domains. Among 205 RXLR effector genes encoding conserved proteins in 17 P. halstedii pathotypes of varying virulence, we selected 30 effectors that were expressed during plant infection as potentially essential genes to target broad‐spectrum resistance in sunflower. The transient expression of the 30 core effectors in sunflower and in Nicotiana benthamiana leaves revealed a wide diversity of targeted subcellular compartments, including organelles not so far shown to be targeted by oomycete effectors such as chloroplasts and processing bodies. More than half of the 30 core effectors were able to suppress pattern‐triggered immunity in N. benthamiana, and five of these induced hypersensitive responses (HR) in sunflower broad‐spectrum resistant lines. HR triggered by PhRXLRC01 co‐segregated with Pl22 resistance in F3 populations and both traits localized in 1.7 Mb on chromosome 13 of the sunflower genome. Pl22 resistance was physically mapped on the sunflower genome recently sequenced, unlike all the other downy mildew resistances published so far. PhRXLRC01 and Pl22 are proposed as an avirulence/resistance gene couple not previously described in sunflower. Core effector recognition is a successful strategy to accelerate broad‐spectrum resistance gene identification in complex crop genomes such as sunflower.     

Effects of growth regulator concentrations and explant size on shoot organogenesis from callus derived from zygotic embryos of sunflower (Helianthus annuus L.)

Effects of medium growth regulator composition and embryo size on shoot organogenesis of callus derived from globular- to torpedo-shaped zygotic embryos of five sunflower (Helianthus annuus L.) genotypes were examined. Forty growth regulator combinations composed of 0 to 5 mgl^-1 naphthaleneacetic acid (NAA) and 0 to 1 mgl^-1 6-benzylaminopurine (BA) were tested. The frequency of zygotic embryos forming shoot-regenerating callus was analysed according to categorical data modelling using a maximum-likelihood approach. Both NAA and BA must be present to induce the formation of morphogenic callus from zygotic embryos, but each growth regulator effect varied with the genotype. For four genotypes, NAA and BA effects were neither linear nor quadratic; whereas, they were linear for the fifth one. Most effective concentrations across genotypes were 0.1 mgl^-1 NAA and 0.5 mgl^-1 or 0.2 mgl^-1 BA. However, the optimal growth regulator combination depended on the genotype and an interaction between the two growth regulators. The frequency of shoot-regenerating callus also varied with the size of the embryo explant. For all five genotypes, 0.4 to 1.2 mm long heart-shaped zygotic embryos formed morphogenic callus more frequently than smaller less-developed ones.     

Reevaluation of biosecurity of Ophraella communa against sunflower (Helianthus annuus)

Ophraella communa (Coleoptera: Chrysomelidae), originally from North America, has been used for biological control of common ragweed, Ambrosia artemisiifolia, in China since 2007. However, there is still a debate on whether O. communa can attack sunflowers under field conditions. To re-evaluate the biosecurity of O. communa against sunflower (Helianthus annuus), we investigated the population density of O. communa on three sunflower varieties that were intercropped with or planted in circumambience of A. artemisiifolia under field conditions. Our results showed that only very few O. communa eggs (<0.5 eggs/plant) were found on sunflower plants at the last two surveys when sunflowers were planted in circumambience of common ragweed. O. communa eggs were not found on sunflower plants at each survey when sunflowers were intercropped with common ragweed. The first–second instar larvae, third instar larvae, pupae and adults of O. communa were occasionally found on sunflower plants, but their densities were very low under either case of planting patterns. Based on these results, we conclude that sunflower is not a potential host plant for O. communa and the beetle is an effective host-specific biological control agent of common ragweed.     

Effect of timing and exposure of sunflower pollen on a common gut pathogen of bumble bees

1. Several bee species are declining due to multiple factors, including pathogens. Ingestion of sunflower (Helianthus annuus) pollen can dramatically reduce the bumble bee gut pathogen Crithidia bombi, but little is known about how timing and exposure to sunflower pollen consumption affects pathogen load. 2. Two experiments were carried out to investigate how exposure to sunflower pollen relative to pathogen exposure affects Crithidia bombi in Bombus impatiens. Foraging trials with pollen‐producing and male‐sterile (pollen absent) sunflower lines were performed to investigate whether sunflower pollen affected pathogen transmission in a single foraging bout, and 7‐day laboratory trials were done to investigate whether timing and duration of exposure to sunflower pollen after infection affected C. bombi. 3. In foraging trials, pollen presence on inflorescences inoculated with C. bombi did not affect transmission (pathogen cell counts of foraging workers) 1 week later, suggesting that a brief experience with sunflower pollen concurrent with pathogen exposure is insufficient to reduce infection. In laboratory trials, consuming sunflower pollen for the first 3.5 days or all 7 days after infection reduced cell counts compared with a negative control pollen, but consuming sunflower pollen starting 3.5 days after infection did not. Consuming sunflower pollen for 7 days was significantly and substantially more effective than any other treatment. Thus, both duration and timing of exposure to sunflower pollen may affect pathogen load. 4. These results are important for understanding ecological disease dynamics in natural settings with free‐flying bumble bees, and may inform decisions about using medicinal diets to manage bumble bee health commercially.     

Agrobacterium-mediated transformation of sunflower (Helianthus annuus L.) shoot apices: transformation patterns

Apical segments of embryonic axes of sunflower (Helianthus annuus L.) embryos were submitted to co-culture experiments with a disarmed strain of Agrobacterium tumefaciens, harbouring a plasmid coding for the marker enzyme -glucuronidase. The expression patterns of this marker were analysed at different developmental stages of the regenerated shoots. The results are consistent with the hypothesis that transformed shoots originate from transformation events that have occurred within the existing meristems. Two of the resulting chimaeric plants have been analysed in detail, and some representative gene integration patterns are presented.     

Influence of four host‐plants on feeding,growth and reproduction of Diacrisia casignetum (Lepidoptera: Arctiidae)

Effects of four host‐plants, sunflower, castor, jute and sesame, on feeding, growth and reproduction of Diacrisia casignetum Kollar (Lepidoptera: Arctiidae) were studied under laboratory conditions (27 ± 0.5°C, 12 h light : 12 h dark, 65 ± 5% RH). Total larval developmental time of D. casignetum was highest on sesame than the other three host‐plants used in this study, but pupal duration was higher on sesame than sunflower but not for other dietary treatments. The longevity of females was generally longer than males. Male and female longevity was higher in sunflower than sesame (P < 0.05), but it did not differ significantly among other treatments. Fecundity was highest in sunflower followed by castor, jute and sesame. The growth and development of D. casignetum were related to nutrient and phenol contents of these four host‐plants. Total carbohydrates and amino acids were present in rich quantities in sunflower when compared to other three host leaves, while nitrogen, protein and lipid contents were comparatively higher in sunflower and castor than jute and sesame. Phenol content was greatest in sesame, and least in castor and sunflower. Higher levels of total carbohydrates, proteins, lipids, nitrogen and amino acids including water content and lower phenol content of sunflower have influenced higher growth rate and fecundity of D. casignetum.     

Unsaturated Fatty Acid Synthesis During the Development of Isolated Sunflower (Helianthus annuus L.) Seeds

The effect of temperature on unsaturated fatty acid synthesisin developing sunflower seed embryos (Helianthus annuus L.)has been studied using isolated seeds grown in culture. Variabilitybetween individual embryos in the response to temperature wasalso investigated. Oil and dry matter accumulation in cultured embryos were similarto those of embryos allowed to develop in intact plants, andthe effect of increasing temperature in lowering the amountof linoleic acid in seed oil was reproduced in cultured embryos.The isolated seed culture system, therefore, constitutes a suitablemodel system for studies of oil synthesis in developing sunflowerembryos. The decrease in linoleic acid synthesis in response to highertemperature was detectable after only 18 day-degrees incubation,and the incorporation of labelled substrates suggests that alterationsin the fatty acid composition of seed oil in response to temperatureare produced by an effect on the desaturation of newly synthesizedoleate rather than through turnover of existing lipid. Variation in fatty acid composition between individual embryosgrown at constant temperature was considerable. The detectionof embryos with high linoleic acid levels following growth athigh temperature indicates that potential may exist for theselection of cultivars for temperature-stable fatty acid compositionin sunflower oil. Key words: Fatty acid synthesis, Helianthus annuus, Sunflower seeds     

Diazacon Inhibits Reproduction in Invasive Monk Parakeet Populations

Abstract: Throughout the United States, managers lack safe, effective methods to control expanding populations of the invasive monk parakeet (Myiopsitta monachus). Because the reproductive inhibitor diazacon (20,25 diazacholesterol) has been used effectively in captive monk parakeets, we provided diazacon-treated sunflower seeds to birds at electric utility substations inhabited by parakeets in south Florida, USA. Nest productivity (nestlings plus eggs with embryos) averaged 1.31 (SE = 0.45, n = 100 nests) at 6 treated sites compared to 4.15 (SE = 0.68, n = 50 nests) at 4 untreated sites, a 68.4% reduction. Exposure of native bird species to treated bait was infrequent. Diazacon is an effective means to reduce reproductive success of monk parakeets, and development of methods to limit exposure of nontarget birds will enable more widespread use of this useful population management technique.     

Morphology,phylogeny and pathogenicity of Alternaria species,involved in leaf spot disease of sunflower in northern Iran

Leaf spot disease of sunflower is one of the most important foliar diseases on this crop worldwide. Several fungal groups are known to cause leaf spot disease on sunflower. Species of the genus Alternaria are the most common and serious leaf spot causing fungi on this crop. Leaf spot disease is the most destructive foliar diseases on sunflower in northern Iran; however, the identity of the causal agent remains unknown. The present study was aimed to characterise the identity of the causal agent of the disease by means of morphological and molecular data as well as to evaluate the pathogenicity of the responsible species. For this purpose, a total number of 97 fungal isolates were recovered from sunflower leaves with leaf spot disease symptoms from the sunflower fields in northwestern zone of Iran. All of the isolates were identified as Alternaria alternata based on cultural and morphological characteristics. A subset of isolates was subjected to phylogenetic analysis using sequence data from ITS-rDNA region, gpd and rpb2 genes. Sequence data from ITS-rDNA and gpd did not discriminate A. alternata from the other small-spored Alternaria species. A phylogeny inferred using sequence data from rpb2 gene clustered our isolates in several sub-clades within a single monophyletic clade. Sequence data for the type strain of the other small-spored Alternaria species has to be included in phylogenetic analysis, in order to make sure, whether the observed variations in rpb2 gene sequences are an indication for the population variation in sunflower isolates of A. alternata or define species boundaries among the small-spored Alternaria species. The results of pathogenicity assay on sunflower plants (cultivar Euroflor) under greenhouse condition revealed that A. alternata is pathogenic on sunflower.     

Laboratory Efficacy of Chemical Repellents for Reducing Blackbird Damage in Rice and Sunflower Crops

Abstract: Nonlethal alternatives are needed to manage blackbird (Icterids) damage to rice and sunflower production in the United States. We evaluated 4 registered fungicides on rice seeds (i.e., Allegiance® FL, Thiram 42-S, Trilex®, and Vitavax® 200 preplant seed treatments) and 2 foliar pesticides on sunflower seeds (Cobalt™ insecticide and Flock Buster bird repellent) as candidate blackbird repellents. Red-winged blackbirds (Agelaius phoeniceus) preferred untreated rice relative to rice treated with Thiram (P < 0.001) and Vitavax (P < 0.001), and untreated sunflower relative to sunflower treated with Cobalt (P < 0.001). Blackbirds preferred untreated sunflower relative to sunflower treated with Flock Buster repellent on day 1 of a 4-day preference test (P < 0.001). We observed no difference in consumption of treated versus untreated rice during the Allegiance preference test (P = 0.928), and blackbirds preferred rice treated with Trilex relative to untreated rice (P = 0.003). Although repellency was positively related to tested concentrations of Thiram (P = 0.010), Trilex (P = 0.026), and Vitavax (P < 0.001), maximum repellency was < 50% during our concentration-response tests of these seed treatments. Repellency was also positively related to tested concentrations of Cobalt (P < 0.001), and we observed >80% repellency of sunflower treated with Cobalt at ≥50% of the label rate. We observed no concentration-response relationship for the Allegiance seed treatment (P = 0.341) and Flock Buster repellent (P = 0.952). We recommend implementation of supplemental field studies to compare laboratory efficacy, repellency, and chemical residues of effective avian repellents throughout periods of needed crop protection.     

Somatic embryogenesis and organogenesis induced on the immature zygotic embryo of sunflower (Helianthus annum L.) cultivated in vitro: role of the sugar

Summary Immature zygotic embryos of sunflower constitute an experimental system where the change of a single key factor (sucrose concentration) conditions the in vitro morphogenesis to either organogenesis (87 mM sucrose) or somatic embryogenesis (350 mM sucrose). Experiments with a variety of culture media differing in the sugar type and concentration, as well as osmotic pressure, indicate that a minimal threshold level of both, sugar supply and osmotic pressure, are required for somatic embryogenesis, but not organogenesis, to occur. The nature of the sugar used, though, was less important.Abbreviations IZE immature zygotic embryo