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  • Author or Editor: J. Yu x
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Temperature is an important environmental factor that affects lettuce (Lactuca sativa L.) germination. The present research was conducted to determine the role of seed coverings on lettuce seed germination at high temperature. Five lettuce genotypes were primed in order to bypass thermoinhibitional effects on germination. During germination of primed and nonprimed seeds, imbibition followed a normal triphasic pattern. Primed seeds had higher final water content, a decreased imbibitional phase II, and germinated at 36 °C compared to nonprimed seeds of thermosensitive genotypes, which did not germinate at 36 °C. Puncture tests were conducted to determine the force required to penetrate the whole seed or endosperm of the five genotypes at 24 and 33 °C. `Dark Green Boston', a thermosensitive genotype, had the highest mean resistance (0.207 N) and PI 251245, a thermotolerant genotype, had the lowest (0.139 N). Resistance to penetration of the endopserm of the five genotypes was different at both temperatures. However, three thermotolerant genotypes had lower endosperm resistance than two thermosensitive types. At 36 °C, the penetration force for primed and nonprimed seeds was compared after the first hour of imbibition and 1 hour before radicle protrusion. The force required to penetrate the seed was affected by genotype, seed priming, and duration of imbibition. Puncture force decreased as imbibition time at 36 °C increased in primed and nonprimed seed of each thermotolerant genotype but not in the thermosensitive genotypes. Priming reduced the initial force necessary to penetrate the seed and endosperm in all genotypes. Thus, for radicle protrusion to occur, there must first be a decrease in the resistance of the endosperm layer as evidenced by priming or thermotolerant genotype. Then, the pericarp and integument are sufficiently weakened so that tissue resistance is lower than the turgor pressure of the expanding embryo, allowing germination to be completed.

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Dollar spot, caused by Sclerotinia homoeocarpa F.T. Bennett, is an important disease of creeping bentgrass (Agrostis stolonifera L.) on golf courses in the northern United States. Canopy moisture in the form of dew plays an important role in the development of dollar spot and routine displacement has been shown to reduce disease severity. The use of plant growth regulators (PGRs) is a common management practice for maintaining creeping bentgrass fairways, but their influence on dollar spot is unclear. The objective of this field study was to elucidate the influence of dew removal at the time of fungicide application on dollar spot control in creeping bentgrass regulated by trinexapac-ethyl (TE). Main factors in the study included three dew removal strategies (non-treated, dew removed–mowed, and dew removed–not mowed) before the application of four fungicide treatments (non-treated, chlorothalonil, propiconazole, and iprodione). All fungicide treatments were applied once to turfgrass previously treated with TE or not treated. The presence or absence of dew at the time of fungicide application generally had no influence on fungicide performance with respect to dollar spot control. Based on the results of this study, dew removal before the application of fungicides targeting dollar spot is unnecessary. Applications of TE before fungicides reduced dollar spot severity in some cases, but reductions in symptom expression were limited and did not result in markedly improved dollar spot control.

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Lettuce (Lactuca sativa L.) seeds can fail to germinate at temperatures above 24 °C. The degree of thermotolerance is thought to be at least partly related to the environment under which the seed developed. In order to study the effects of temperature during seed development on subsequent germination, various lettuce genotypes were screened for their ability to germinate at temperatures ranging from 20 to 38 °C. Seeds of the selected genotypes `Dark Green Boston' and `Valmaine' (thermosensitive), `Floricos 83', `Everglades', and PI 251245 (thermotolerant) were produced at 20/10, 25/15, 30/20, and 35/25 °C day/night temperature regimes in plant growth chambers. Seeds were germinated on a thermogradient bar from 24 to 36 °C under 12 h light/dark cycles. As germination temperature increased, the number of seeds that failed to germinate increased. Above 27 °C, seeds matured at 20/10 or 25/15 °C exhibited a lower percent germination than seeds that matured at 30/20 or 35/25 °C. Seeds of `Dark Green Boston' and `Everglades' that matured at 30/20 °C exhibited improved thermotolerance over those that matured at lower temperatures. Seeds of `Valmaine' produced at 20/10 °C exhibited 40% germination at 30 °C, but seeds that matured at higher temperatures exhibited over 95% germination. Germination of `Valmaine' at temperatures above 30 °C was not affected by seed maturation temperature. The upper temperature limit for germination of lettuce seed could thus be modified by manipulating the temperature during seed production. The potential thermotolerance of seed thereby increased, wherein thermosensitive genotypes became thermotolerant and thermotolerant genotypes (e.g., PI251245) germinated fully at 36 °C. This information is useful for improving lettuce seed germination during periods of high soil temperature, and can be used to study the biology of thermotolerance in lettuce.

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Thermotolerance in lettuce seed at high temperature was investigated using primed and nonprimed seed or seeds matured at 20/10°C and 30/20°C. During seed germination at 36°C, the structural changes of the seed coverings in front of the radicle tip were observed in an anatomical study. In all seeds during imbibition, regardless of seed maturation temperature or priming, a crack appeared on one side of the cap tissue and the endosperm separated from the integument in front of the radicle tip. Additional changes took place during imbibition: the protein bodies in the vacuoles enlarged and were gradually depleted, large empty vacuoles formed, the cytoplasm condensed, the endosperm shrank, the endosperm cell wall dissolved and ruptured, then the radicle elongated toward this ruptured area. The findings suggested that the papery endosperm layer presented mechanical resistance to lettuce seed germination and the weakening of this layer was a prerequisite to radicle protrusion at high temperature. Seeds of `Dark Green Boston', `Everglades', and PI 251245 matured at 30/20°C had greater thermotolerance than those matured at 20/10°C. Results of the anatomical study indicated that the endosperm cell walls in front of the radicle of seeds matured at 30/20°C were more easily disrupted and ruptured during early imbibition than seeds matured at 20/10°C, suggesting that these seeds could germinate quickly at supra-optimal temperatures. From anatomical studies conducted to identify and characterize thermotolerance in lettuce seed germination, it was observed that genotype thermotolerance had the ability to reduce physical resistance of the endosperm by weakening the cell wall and by depleting stored reserves.

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A randomly amplified polymorphic DNA (RAPD) technique was used to identify and determine the phylogenetic relationships of 37 hosta accessions representing the major subgenera, sections and groups in the genus Hosta. Results of this study show that RAPD markers were able to differentiate not only the main groups, whose plants shared many genetic traits, but also cultivars within a species. Some accessions were identified by a single primer while others had high intercross linkage and required many markers for their separation. The phylogenetic clustering showed that H. plantaginea, the only night-blooming species, and H. ventricosa, the only known natural tetraploid, are unique and should be classified separately. The four species in the subgenus Bryocles, section Lamellatae H. venusta, H. minor, H. capitata, and H. nakaiana have very low genetic similarity since they do not share many amplified fragments. The other accessions were classified into four main clusters; cluster 1: H. venusta, H. tardiva, H. pycnophylla, H. tsushimensis `Ogon', H. montana, H. tibae, H. montana f. macrophylla, H. kikutii `Kikutii', H. longissima `Longifolia', H. rectifolia `Rectifolia', H. takahashii and H.`Undulata'; cluster 2: H. laevigata, H. sieboldiana, H. pycnophylla × H. longipes f. latifolia, H. longipes `Urajiro' and H. ibukiensis; cluster 3: H. capitata, H. kikutii `Polyneuron', H. nigrescens, H. kikutii `Yakusimensis', H. pachyscapa, H. kikutii `Caput-Avis', H. longipes f. latifolia, H. hypoleuca, H. okamotoi, H. densa and H. takiensis; and cluster 4: H. aequinoctiiantha, H. rupifraga, H. `Amanuma', H. minor and H. kikutii `Densa'.

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The aroma volatiles of ripe fresh `GoldRush' and `Golden Delicious' apples (Malus ×domestica Borkh) were examined using dynamic headspace to capture the volatiles and gas chromatography (GC)–GC–mass spectroscopy (MS) analysis for compound identification. A total of 21 aroma volatiles were identified, with 16 being common to both cultivars: toluene, butyl acetate, hexyl formate, 2-methylbutyl acetate, xylene, butyl propionate, pentyl acetate, s-butyl butanoate, hexyl acetate, iso-butyl 2-methylbutanoate, hexyl propionate, hexyl butanoate, hexyl 2-methylbutanoate, hexyl hexanoate, a-farnesene, and ethyl phthalate. Three volatiles [dipropyl disulfide, pentyl 2-methylpropionate, and 2,6-bis(1,1-dimethylethyl)-2,5-cyclohexadiene-1,4-dione] were unique to `Golden Delicious'; two compounds (nonanal and nerolidol) were unique to `GoldRush'. Most identified compounds were esters. Hexyl acetate (18.39%) was the major volatile in `Golden Delicious', while butyl acetate (13.40%) was the highest in `GoldRush'.

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The volatiles of muskmelon (Cucumis melo L. reticulatis cv. Mission) were sampled by dichloromethane extraction and dynamic headspace methods and analyzed by gas chromatography (GC) and GC–mass spectroscopy (MS). A total of 34 constituents were identified, with esters contributing 8%–92% of the total volatiles. Butyl propionate, ethyl 3-methylpentanoate, hexadecanoic acid, methyl (methylthio)acetate, propyl butyrate, phenylpropyl alcohol, and vanillin, were recovered only by solvent extraction, while hexanal was only detected using dynamic headspace sampling. Methyl butyrate 35.2%, ethyl acetate 17.1%, butyl acetate 11.6%, ethyl propionate 8.3%, and 3-methylbutyl acetate 6.3% were the major constituents by solvent extraction sampling method. Butyl acetate 35.5%, 3-methylbutyl acetate 20.9%, ethyl acetate 7.3%, 2-butyl acetate 5.6%, and hexyl acetate 3.8% were the major constituents recovered by headspace sampling. Fruit tissue was also separated into five layers (exocarp, outer mesocarp, middle mesocarp, inner mesocarp, and seed cavity) and the volatile constituents differed significantly in content and composition by tissue.

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Two random amplified polymorphic DNA (RAPD) markers linked to En, the gene conferring resistance to pea enation mosaic virus in pea, were identified and the DNA fragments were cloned and partially sequenced. Allele-specific associated primers for each cloned DNA fragment were developed and used in screening F2 populations. One marker, P256900, mapped very near Adh-1, about 6 cM from En. The other marker, B500400, was located about 8 cM from En on the same side as P256900.

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In Florida, cabbage (Brassica oleracea L.) is typically grown without a plastic mulch and as a result, weeds are a significant problem in most fields. Experiments were conducted from Nov. 2015 to Apr. 2016 in Balm, Citra, and Parrish, FL, to evaluate weed control and ‘Bravo’ cabbage tolerance to multiple herbicide programs applied pretransplanting (PRE-T), posttransplanting (POST-T), PRE-T followed by (fb) a sequential application at 3 weeks after transplanting (WATP), and POST-T fb sequential application at 3 WATP. PRE-T herbicide treatments of 277 g a.i./ha clomazone, 280 g a.i./ha oxyfluorfen, and 798 g a.i./ha pendimethalin and POST-T herbicide treatments of 6715 g a.i./ha dimethyl tetrachloroterephthalate (DCPA) were ineffective, and weed control never exceeded 70% in Balm and provided <50% weed control in Citra and Parrish at 6 and 8 WATP, respectively. POST-T applications of napropamide + S-metolachlor at 2242 + 1770 g a.i./ha, DCPA + S-metolachlor at 6715 + 1170 g a.i./ha, and S-metolachlor POST-T fb clopyralid at 1170 g a.i./ha fb 210 g ae/ha were the most effective herbicide treatments and consistently provided >70% weed control. In addition, results showed that all of the herbicide treatments evaluated except the PRE application of clomazone at 277 g a.i./ha are safe for cabbage with no adverse effect on yield.

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Petunia ×hybrida (Hook) Vilm. cv. Mitchell was transformed with an E. coli gene encoding mannitol-1-phosphate dehydrogenase (mtlD). Four plant lines that grew on kanamycin and contained the mtlD transgene were identified. Two of these lines contained high levels of mannitol [high-mannitol lines M3 and M8; mean mannitol = 3.39 μmol·g-1 dry weight (DW)] compared to nontransformed wild-type plants (0.86 μmol·g-1 DW), while two lines had mannitol levels similar to wild-type plants (low-mannitol lines M2 and M9; mean mannitol = 1.05 μmol·g-1 DW). Transgenic and control plants were subjected to chilling stress (3 ± 0.5 °C day/0 ± 0.5 °C night, 12-hour photoperiod and 75% relative humidity) to evaluate the role of mannitol in chilling tolerance. Based upon foliage symptoms and membrane leakage after a 3-week chilling treatment, the high-mannitol containing lines, M3 and M8, were more tolerant of chilling stress than the low-mannitol containing transgenic lines, M2 and M9, and wild-type. Under nonchilling conditions mannitol was the only carbohydrate that differed among transgenic lines, but all carbohydrates were present. When subjected to chilling stress, mannitol levels dropped by 75%, sucrose by 52%, and inositol by 54% in the low-mannitol lines (M2 and M9). In M3 and M8, the high-mannitol lines, mannitol levels decreased by 36%, sucrose by 25%, and inositol by 56%, respectively. Raffinose increased 2- to 3-fold in all lines following exposure to low-temperature chilling stress. In the higher mannitol lines only 0.04% to 0.06% of the total osmotic potential generated from all solutes could be attributed to mannitol, thus its action is more like that of an osmoprotectant rather than an osmoregulator. This study demonstrates that metabolic engineering of osmoprotectant synthesis pathways can be used to improve stress tolerance in horticultural crops.

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