Littérature scientifique sur le sujet « Dieffenbachia »
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Articles de revues sur le sujet "Dieffenbachia"
Henny, R. J., C. A. Conover et R. T. Poole. « ‘Victory’ Dieffenbachia ». HortScience 22, no 5 (octobre 1987) : 967–68. http://dx.doi.org/10.21273/hortsci.22.5.967.
Texte intégralJouen, E., P. Laurent, I. Robène-Soustrade, L. Gagnevin, O. Pruvost, B. Hostachy, G. Gateblé, R. Amice et F. Imbert. « First Report in New Caledonia of Bacterial Blight of Anthurium Caused by Xanthomonas axonopodis pv. dieffenbachiae ». Plant Disease 91, no 4 (avril 2007) : 462. http://dx.doi.org/10.1094/pdis-91-4-0462b.
Texte intégralNorman, D. J., R. J. Henny, J. M. F. Yuen et E. R. Dickstein. « First Report of Xanthomonas axonopodis Infecting Agapanthus in Florida ». Plant Disease 86, no 5 (mai 2002) : 562. http://dx.doi.org/10.1094/pdis.2002.86.5.562a.
Texte intégralNorman, D. J., R. J. Henny et J. M. F. Yuen. « Disease Resistance in Twenty Dieffenbachia Cultivars ». HortScience 32, no 4 (juillet 1997) : 709–10. http://dx.doi.org/10.21273/hortsci.32.4.709.
Texte intégralHenny, R. J., C. A. Conover et R. T. Poole. « ‘Triumph’ Dieffenbachia ». HortScience 22, no 5 (octobre 1987) : 965–66. http://dx.doi.org/10.21273/hortsci.22.5.965.
Texte intégralHenny, R. J., J. Chen et D. J. Norman. « `GoldRush' Dieffenbachia ». HortScience 39, no 6 (octobre 2004) : 1505–6. http://dx.doi.org/10.21273/hortsci.39.6.1505.
Texte intégralHenny, R. J. « `Sparkles' Dieffenbachia ». HortScience 30, no 1 (février 1995) : 163. http://dx.doi.org/10.21273/hortsci.30.1.163.
Texte intégralHenny, R. J., J. Chen et D. J. Norman. « `Sterling' Dieffenbachia ». HortScience 41, no 5 (août 2006) : 1356. http://dx.doi.org/10.21273/hortsci.41.5.1356.
Texte intégralHasanah, Hasni Ummul, et Evi Hanizar. « Pengaruh Ekstrak Daun Bahagia (Dieffenbachia Sp.) terhadap Mortalitas Kecoa (Periplanetta Sp.) ». BIO-CONS : Jurnal Biologi dan Konservasi 5, no 1 (15 juin 2023) : 269–77. http://dx.doi.org/10.31537/biocons.v5i1.1143.
Texte intégralHenny, R. J., R. T. Poole et C. A. Conover. « `Star White' Dieffenbachia ». HortScience 27, no 1 (janvier 1992) : 82–83. http://dx.doi.org/10.21273/hortsci.27.1.82.
Texte intégralThèses sur le sujet "Dieffenbachia"
Hudson, G. « Micropropagation and low temperature storage of Dieffenbachia ». Thesis, University of East London, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370763.
Texte intégralCao, Hui. « The distribution of calcium oxalate crystals in genus Dieffenbachia schott. and the relationship between environmental factors and crystal quantity and quality ». [Gainesville, Fla.] : University of Florida, 2003. http://purl.fcla.edu/fcla/etd/UFE0001245.
Texte intégralDonahoo, Ryan Scott. « Genetic variation in Xanthomonas axonopodis pv. dieffenbachiae ». [Gainesville, Fla.] : University of Florida, 2003. http://purl.fcla.edu/fcla/etd/UFE0000676.
Texte intégralBERTHIER, YVETTE. « Caracterisation de xanthomonas campestris pathovar dieffenbachiae : etude serologique et moleculaire ». Paris 11, 1993. http://www.theses.fr/1993PA112289.
Texte intégralDieffenbacher, Frank [Verfasser]. « Untersuchung zur Parasitenfauna von verwilderten Hauskatzen und deren Behandlung mit Selamectin und Praziquantel / Frank Dieffenbacher ». Berlin : Freie Universität Berlin, 2007. http://d-nb.info/1022493949/34.
Texte intégral劉祖惠. « The tissue culture of Dieffenbachia ». Thesis, 1990. http://ndltd.ncl.edu.tw/handle/83314905429411437685.
Texte intégralHsiao, Yi Yun, et 蕭伊芸. « Micropropagagtion and mutation of Dieffenbachia maculata‘Rudolph Roehrs-86-A’ ». Thesis, 2002. http://ndltd.ncl.edu.tw/handle/10955667294211393359.
Texte intégral國立中興大學
園藝學系
90
Shoot regeneration through callus culture was induced successfully from young expanded leaves of Dieffenbachia maculata ‘Rudolph Roehrs-86M1’in vitro. Young leaves were cut into 1 ×1cm pieces and surface sterilized in 0.5% sodium hypochlorite for 10 min followed by washing with sterile distilled water. The contamination was controlled under 25%. Leaves were cultured on the medium containing 1/2 MS, sugar 20g/l, agar 6g/l, BA 5 mg/l and NAA 0.5 mg/l and were induced more callus . Shoot proliferated when callus explant of 5mm in cubic was cultured on the medium containing 1/2 MS, agar 6g/l, sugar 20g/l, BA 5 mg/l and NAA 0.125 mg/l. Shoot longer than 2.5 cm rooted well when shoot base was coated with NAA 0.1%. There was 50% or 66.7% of callus proliferating shoot, when callus of 5mm×5mm was irradiated 4 Gy γ-ray once or twice, respectively. However, callus of 10mm×10mm was irradiated once, the rate of shoot proliferation increased to 76.8%. And there was 50% of callus proliferating shoot when irradiated twice.
Castro, Dip Etyene. « Eugenol e a intoxição por "comigo-ninguém-pode" (Dieffenbachia Picta Schott) ». Master's thesis, 2002. http://hdl.handle.net/10316/89077.
Texte intégralDieffenbachia picta Schott. (Araceae), conhecida no Brasil as “comigo ninguém pode” é uma planta ornamental cujas propriedades tóxicas do suco do caule da planta quanto em contato com a boca ou aspirado são responsáveis por casos de intoxicação em crianças e animais domésticos.
Shen, Rong-Show, et 沈榮壽. « Establishment of regeneration system via axillary bud culture and somatic embryogenesis in Dieffenbachia spp ». Thesis, 2006. http://ndltd.ncl.edu.tw/handle/40432932873352768845.
Texte intégral國立臺灣大學
園藝學研究所
94
In this research the influence of pathogen-free explant preparation on aseptic culture and shoot proliferation in Dieffenbachia ‘Starshine’ was study. Using different sizes of apical meristem as initial pathogen-free explants and cultured on solidified Murashige and Skoog (MS) medium with 1mg/L NAA and 1mg/L TDZ for 15 weeks. The 20% of survival rate were obtained from the minimum size (0.1x0.25mm) of shoot tip explant, and 12.3 shoots were regenerated from the larger size (0.9x1.2mm) of shoot tip explant during primary aseptic culture. Moreover, tests used 4 sizes of axillary bud meristem as initial pathogen-free explant for primary aseptic culture. Result demonstrates that removed 3 or 4 coleoptiles of axillary bud explant, gave the survival rate of 30-35%. But, on average, 11.2 shoots regenerated from excided 1 coleoptile of axillary bud explant. These results indicated using apical meristem as pathogen-free explant gave optimize information for primary aseptic culture in Dieffenbachia ‘Starshine. Furthermore, pretreatment of stock plants with 6-week drought stress and further dissected axillary bud under aseptic condition as pathogen-free explants for primary aseptic culture. Results show the explant preparation procedure gave the high survival rate was 80-92.5% from removed 2-4 coleoptiles of axillary bud explant. This result suggests using axillary bud explant dissection and treating with drought stress could escape contamination from the interior contaminants. At the same procedure, more than 90% of survival rate was observed in axillary bud explants for successfully established of primary aseptic culture between tested cultivars(D. cv. Rudolph Roehrs and D. cv. Jupiter). In addition, the influence of culture methods and TDZ concentration on shoot multiplication were investigated. For shoot multiplication, concentration of 1, 5, and 10mg/L TDZ in the liquid culture were found that shoot yields have a significant effect achieved 5-6 folds. While, 2-nodal explant was cultured in liquid medium only obtained 2 folds of multiplication rate, but compared to solid culture, the regenerated shoots were more rapid growth and uniformity during subculture. This result suggests that liquid culture can significantly enhance axillary shoot proliferation from stock stem explants and 2-nodal explants for mass multiplication in Dieffenbachia seedlings. A rapid and efficient procedure is described for mass multiplication of microshoots using temporary immersion system (TIS) in dieffenbachia (Dieffenbachia ‘Starshine’). Multiple shoot proliferation was induced from 2-nodal and stock-stem explants on Murashige and Skoog (MS) media supplemented with 1 mg/L NAA and 0.1-5.0 mg/L thidiazuron (TDZ) or BA. Especially, the 2-nodal or stock-stem explants cultured under TIS on 5mg/L TDZ enriched medium had the highest shoot yield which was 24.5 and 59.2, respectively, the multiplication rate increased by 3.3-8 folds, over that obtained from conventional solid support systems. Therefore, the scheme for the rapid microshoot propagation of dieffenbachia using temporary immersion system had commercial efficiency. In addition, elongated multiple shoots after acclimatization, taken from the temporary immersion system, pretreated with 500mg/dm3 NAA then were cut and planted in plug with soilless mix under mist propagation condition to prevent desiccation. Survival was investigated after 30 days, microshoots taller than 3.0㎝ had the highest survival rate, which achieved 80-100%. Moreover, the shoot cluster was segmented into 1/4 or 1/2 section as propagules; the survival rate was 83.3-100%. In this production scheme, shoot cluster could be established a system of superior stock-plant for use in dieffenbachia cuttage. A method for the somatic embryogenesis and subsequent plant regeneration for Dieffenbachia ‘Tiki’ hybrids was described. Male inflorescence explants isolated from spadix of flowering plants cultured in vitro, formed embryogenic calli on surfaces of inflorescence axis within eight weeks of culture on full-strength Murashiage and Skoog (MS) medium with 4-6 mg/L 2,4-D. Somatic embryogenesis and embryoid were induced using a modified half-strength MS combination of 2 % sucrose with 1 % glucose, 0.18 % Gelrite for the basal medium, supplemented with 4.0 to 5.1 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.5 mg/L Kinetin. Male inflorescence explants transfer to modified half-strength MS basal medium with 0.5mg/L Kinetin and 4mg/L 2,4-D(or 2-4mg/L Dicamba)resulted in somatic embryogenesis at frequencies of 45-72.1% with an average of 13.3-22.2 somatic embryos per responding explant. Furthermore, at the same culture condition, male inflorescence explants were cultured onto half-strength MS basal medium with 4mg/L 2,4-D and 0.5-1.0mg/L Thidiazuron(TDZ) for embryogenesis. TDZ was found to increase the somatic embryogenesis frequencies to 100% with an average of 32.1-38.2 somatic embryos per responding explant. At the same condition, a few somatic embryos developed into complete plantlets. In this study, we are the first to report somatic embryogenesis in Dieffenbachia ‘Tiki’ and the conversion of somatic embryos to greenhouse-established plant. A regeneration system for improving the efficiency of somatic embryogenesis and emblings recovery from male inflorescences and somatic embryos of Dieffenbachia ‘Tiki’ were described. The highest percentage (100%) of primary somatic embryogenesis were achieved, and the highest yield of mature primary embryos were 75.5 on the half strength modified Murashige and Skoog(MS)medium with 2mg/L Dicamba and 0.5mg/L TDZ from male inflorescence explants. The results indicated that combination of Dicamba (2mg/L) and TDZ (0.5mg/L) significantly promoted high-efficiency multiplication of mature primary embryos in Dieffenbachia ‘Tiki’. Furthermore, the mature embryos of primary somatic embryogenesis were used as initial secondary explants for the induction of repetitive somatic embryogenesis. On the same culture medium supplemented with 2mg/L Dicamba and 0.5-1.0mg/L TDZ, the highest frequency (100%) of secondary embryo formation was obtained after 8-week subculture, and the highest number of mature secondary embryos per explant achieved 33.0-34.3 after 13-week subculture. Consequently, the same medium compositions were suitable for efficient repetitive somatic embryogenesis and multiplication of secondary embryos. In addition, emblings conversion of mature secondary embryos was investigated. The green secondary embryos of 4-5mm in size and the age of 8-10 weeks were used as explants, and cultured on half strength modified MS supplemented with 150mL/L coconut milk for somatic embryo conversion. The highest converted frequency of somatic embryo were 73.3%, and the number of converted emblings per explant reached 7.8 at 0.5% glucose and 1.0mg/L TDZ combination. Plantlets conversion from embryo was successfully acclimatized to greenhouse conditions. This technique could have significant industry application in dieffenbachia micropropagation, based on it has high efficiency of somatic embryo formation and high level of plant recovery.
Tsai, Yao-Lung, et 蔡曜隆. « Induction and proliferation of somatic embryo,emblings conversion and axillary buds multiplication in Dieffenbachia ‘Anna’ ». Thesis, 2004. http://ndltd.ncl.edu.tw/handle/64091275229082120197.
Texte intégral國立嘉義大學
園藝學系研究所
94
A procedure for the induction, proliferation, emblings conversion of somatic embryo and axillary buds multiplication in Dieffenbachia ‘Anna’ was described. The male inflorescence explants were isolated and cultured on 1/2 Murashige and Skoog (MS) medium with 1% glucose, 2% sucrose, 3% Gelrite as the basal medium. Embryogenesis callus was induced and had the best growth index on medium with 4 mg/L Dicamba and 1-2 mg/L Thidiazuron (TDZ), the percentage of forming somatic embryo were 69.4-90.4% with an average of 41.7-43.7 somatic embryos per explant. Furthermore, at the same culture condition, primary somatic embryo explants were cultured on 1/2 MS basal medium with 1-2 mg/L 2,4-D or 1-2 mg/L Dicamba and 1-2 mg/L Dicamba combined with 2 mg/L TDZ, respectively, the percentage of secondary somatic embryogenesis was 100%. Secondary somatic embryos (SSE) could be obtained with an average of 30-35 embryos on basal medium supplemented with 1 or 4 mg/L Dicamba and 2 mg/L TDZ. At the same test, SSE could be reached with an average of 30 embryos on basal medium added 2-4 mg/L TDZ and 2% glucose. Moreover, the emblings formation of mature somatic embryo was at a frequency of 80% with an average 3.1 emblings on 1/2 MS basal medium supplemented with 150 mL/L coconut milk and 2% glucose, those emblings developed into complete plantlets at the same culture condition. At the same tests, the basal medium with 2-4 mg/L GA3 was found to significantly accelerate SSE developed to coleoptilar stage, and then promote the sheaths elongation. Furthermore, axillary buds multiplication via temporary immersion system (TIS) was invesgated. The shoot proliferation was induced on MS medium supplemented with 1 mg/L NAA and 1mg/L BA, results indicated the shoot yield was 6.1 under 30 min/6hr immersion time, and the basal suitable medium volume was 350 mL. Shoot proliferation crate be obtained from >5cm nodal and stock-stem explants was 5.4-5.5. In this production scheme, a mass-production system could be established from axillary multiplication for Dieffenbachia industry.
Livres sur le sujet "Dieffenbachia"
Hudson, Glyn. Micropropagation and low temperature storage of Dieffenbachia. London : North East London Polytechnic, 1985.
Trouver le texte intégralHudson, Glyn. Micropropagation and low temperature storage of dieffenbachia. London : NELP, 1986.
Trouver le texte intégralKlein, Alain. Dieffenbach-lès-Woerth. Haguenau : Familles d'Alsace du Nord-généalogie, 2010.
Trouver le texte intégralKlein, Alain. Woerth : Localités du bailliage de Woerth, Dieffenbach-lès-Woerth, Eberbach-lès-Woerth, Griesbach et Morsbronn-les-Bains avant 1793. Haguenau : Familles d'Alsace du Nord-généalogie, 2010.
Trouver le texte intégralShantz, Mary C. John & Elizabeth Shupe & descendants : A family history of certain Shupes in North America from the early 18th century to the present : including notes on families of Dieffenbach, Munson, Overholt, Warner, Fulsom, Ahrens, Hirschy, Shantz, & Bock. Sudbury, Ont., Canada : M.C.S. Shantz, 1985.
Trouver le texte intégralDieffenbach, Johann Philipp, J. J. Tanner et F. Heinzerling. Ansichten Von Giessen und Seiner Nachbarschaft. Nach Originalzeichnungen Von F. Heinzerling, in Stahl Gestochen Von J. J. Tanner, Nebst Einem Beschreibenden Texte Von Prof. Dr. P. Dieffenbach. Creative Media Partners, LLC, 2019.
Trouver le texte intégralDieffenbach, Johann Philipp, et J. J. Tanner. Ansichten Von Giessen und Seiner Nachbarschaft. Nach Originalzeichnungen Von F. Heinzerling, in Stahl Gestochen Von J. J. Tanner, Nebst Einem Beschreibenden Texte Von Prof. Dr. P. Dieffenbach. Creative Media Partners, LLC, 2018.
Trouver le texte intégralComplete Triathlon Guide. Human Kinetics, 2012. http://dx.doi.org/10.5040/9781718219304.
Texte intégralChapitres de livres sur le sujet "Dieffenbachia"
Montag, Andreas. « Dieffenbachie (Dieffenbachia seguine) ». Dans Pflanzen und Haut, 441–44. Berlin, Heidelberg : Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-63014-3_33.
Texte intégralHammiche, Victoria, Rachida Merad et Mohamed Azzouz. « Dieffenbachia ». Dans Plantes toxiques à usage médicinal du pourtour méditerranéen, 119–21. Paris : Springer Paris, 2013. http://dx.doi.org/10.1007/978-2-8178-0375-3_16.
Texte intégralSastry, K. Subramanya, Bikash Mandal, John Hammond, S. W. Scott et R. W. Briddon. « Dieffenbachia spp. » Dans Encyclopedia of Plant Viruses and Viroids, 886–89. New Delhi : Springer India, 2019. http://dx.doi.org/10.1007/978-81-322-3912-3_323.
Texte intégralAraus, J. L., R. Calafell, G. Burgos, J. F. Aguila et J. Azcón-Bieto. « Relationship Between Structural Mitochondrial Parameters and Respiration Rates in Variegated Leaves of Dieffenbachia ‘Camilla’ ». Dans Plant Mitochondria, 385–88. Boston, MA : Springer US, 1987. http://dx.doi.org/10.1007/978-1-4899-3517-5_64.
Texte intégralZenkteler, E., K. Włodarczak et M. Kłosowska. « The Application of Antibiotics and Sulphonamide for Eliminating Bacillus Cereus During the Micropropagation of Infected Dieffenbachia Picta Schott ». Dans Pathogen and Microbial Contamination Management in Micropropagation, 183–91. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-015-8951-2_22.
Texte intégralMahendran, Ravindran, Ethan Herng Rwei Lim et Ming Jie Kuan. « Antimicrobial, Antioxidant, Toxicity and Phytochemical Screening of Dieffenbachia Camilla and the Synthesis of a Novel and Green Topical Delivery Method for It ». Dans IRC-SET 2021, 555–68. Singapore : Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-9869-9_44.
Texte intégralTolhurst, David. « Johann Friedrich Dieffenbach (1792–1847) ». Dans Pioneers in Plastic Surgery, 5–7. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-19539-1_3.
Texte intégralProbst, J. « Ehrengedenken für Johann Friedrich Dieffenbach (1792–1847) ». Dans Hefte zur Zeitschrift „Der Unfallchirurg“, 28–31. Berlin, Heidelberg : Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78271-8_5.
Texte intégralWessinghage, D. « Johann Friedrich Dieffenbach : „Der Aether gegen den Schmerz“ ». Dans Geschichte der Grenzgebiete der Orthopädie, 97–109. Heidelberg : Steinkopff, 2002. http://dx.doi.org/10.1007/978-3-642-57510-5_11.
Texte intégralVichev, Yavor, Ralf Neuhaus et Wilhelm Zink. « Kontinuierlicher Verbesserungsprozess (KVP) – Praxisbeispiel Dieffenbacher GmbH Maschinen- und Anlagenbau ». Dans ifaa-Edition, 143–50. Berlin, Heidelberg : Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48552-1_20.
Texte intégralActes de conférences sur le sujet "Dieffenbachia"
Peixoto, Ellen Carvalho, LARA FABIAN RODRIGUES DE JESUS, MARIA GABRIELA DOS PASSOS SANTOS, BRUNO DA SILVA MOTA et JULIANO RICARDO FABRICANTE. « ESTRUTURA POPULACIONAL DA ESPECIES DIEFFENBACHIA SEGUINTE (JACQ) SCHOTT NO PARQUE NACIONAL SERRA DE ITABAIANA SERGIPE BRASIL ». Dans V Congresso Brasileiro de Ciências Biológicas. Revista Multidisciplinar de Educação e Meio Ambiente, 2024. http://dx.doi.org/10.51189/conbracib2024/35694.
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