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Relevant bibliographies by topics / Zinnion

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Academic literature on the topic 'Zinnion'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Zinnion"

1

Gombert, Linda, Mark Windham, and Susan Hamilton. "Evaluation of Disease Resistance among 57 Cultivars of Zinnia." HortTechnology 11, no. 1 (2001): 71–74. http://dx.doi.org/10.21273/horttech.11.1.71.

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Fifty-seven cultivars of zinnia (Zinnia elegans Jacq.) were studied for 17 weeks to determine their resistance to alternaria blight (Alternaria zinniae Pape), powdery mildew (Erysiphe cichoracearum DC ex Merat) and bacterial leaf & flower spot [Xanthomonas campestris pv. zinniae (syn. X. nigromaculans f. sp. zinniae Hopkins & Dowson)]. A disease severity scale was used to determine acceptability for landscape use. At week 4, all cultivars were acceptable. At week 10, eleven cultivars were acceptable. At week 17, all cultivars were unacceptable. Ten cultivars had been killed by one or more pathogens by week 17. Only two cultivars showed any tolerance to any disease (powdery mildew) at week 17.

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Szopińska, Dorota. "Effects of hydrogen peroxide treatment on the germination, vigour and health of Zinnia elegans seeds." Folia Horticulturae 26, no. 1 (2014): 19–29. http://dx.doi.org/10.2478/fhort-2014-0002.

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ABSTRACT The high infestation rate of zinnia (Zinnia elegans Jacq.) seeds with fungi, especially pathogenic Alternaria zinniae, has frequently resulted in a poor germination capacity associated with a high number of abnormal diseased seedlings. The effect of hydrogen peroxide (H2O2) treatment on the germination, vigour and health of zinnia seeds was investigated. Two samples of zinnia seeds - sample I, characterised with a low germination capacity (39.5%) and a high level of seed infection with A. zinniae (76%), and sample II, with a high germination capacity (87%) and free from this pathogen - were tested. For treatment, seeds were soaked in 3%, 6%, 9% and 12% H2O2 solutions for 10, 20, 30 and 60 min. Initially, the controls were seeds soaked in distilled water for 10, 20, 30 and 60 min, and then the results of selected treatments were compared with results obtained for untreated seeds and seeds treated with a fungicide (20% carbendazim and 45% thiram). The fungi Alternaria spp. and Fusarium spp. were frequently identified on tested seeds. The concentration of hydrogen peroxide affected the quality of zinnia seeds to a higher extent than the treatment time. However, all of the treatments applied, regardless of time and concentration of H2O2, positively affected seed health, significantly reducing seed infestation by fungi in both samples. Moreover, the lowest level of A. zinniae infection was observed if seeds were soaked in 6% and 9% H2O2 solutions for 60 and 20 min, respectively. Higher concentrations of H2O2 (9% and 12%) negatively influenced seed germination and vigour, especially in sample II. These findings suggested that the treatment of zinnia seeds with hydrogen peroxide can effectively improve germination mostly in samples heavily infected with pathogens, which means that it should be preceded by seed health evaluation.

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Yeargan, Kenneth V., and Sarah M. Colvin. "Butterfly Feeding Preferences for Four Zinnia Cultivars." Journal of Environmental Horticulture 27, no. 1 (2009): 37–41. http://dx.doi.org/10.24266/0738-2898-27.1.37.

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Abstract Zinnias are recommended frequently for inclusion in butterfly gardens as nectar sources for adult butterflies, but little is known about butterfly preferences for different zinnia cultivars. We compared numbers and species of butterflies that visited four widely available zinnia cultivars: Zinnia violacea Cav. (formerly Zinnia elegans Jacq.) ‘Lilliput’, ‘Oklahoma’, ‘State Fair’, and Zinnia marylandica Spooner, Stimart, and Boyle ‘Pinwheel’. Mixed colors were used for all cultivars. Based on a total count of 2355 butterflies, representing 30 species, more than twice as many total butterflies visited ‘Lilliput’ than visited any of the other cultivars. Also, a greater number of butterfly species visited ‘Lilliput’ than visited any of the other cultivars. More than half of the counted butterflies belonged to the family Nymphalidae, with members of the families Pieridae and Hesperiidae being the second and third most frequent visitors, respectively.

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Boyle, Thomas H., and Robert L. Wick. "Responses of Zinnia angustifolia × Z. violacea Backcross Hybrids to Three Pathogens." HortScience 31, no. 5 (1996): 851–54. http://dx.doi.org/10.21273/hortsci.31.5.851.

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True-breeding lines of Zinnia marylandica Spooner, Stimart & Boyle [allotetraploids of Z. angustifolia H.B.K. and Z. violacea Cav. (2n = 4x = 46)] were backcrossed with autotetraploid Z. angustifolia (2n = 4x = 44) and Z. violacea (2n = 4x = 48). Seed-generated, backcross (BC1) families were screened for resistance to alternaria blight (Alternaria zinniae Pape), bacterial leaf and flower spot [Xanthomonas campestris pv. zinniae (Hopkins and Dowson) Dye], and powdery mildew (Erysiphe cichoracearum DC. ex Merat). All BC1 families exhibited high levels of resistance to alternaria blight and powdery mildew. BC1 families derived from crossing Z. marylandica with autotetraploid Z. angustifolia were highly resistant to bacterial leaf and flower spot, whereas BC1 families derived from crossing Z. marylandica with autotetraploid Z. violacea were susceptible to this disease. Our results suggest that one Z. angustifolia genome in BC1 allotetraploids is sufficient to confer resistance to A. zinniae and E. cichoracearum, but at least two Z. angustifolia genomes are required in BC1 allotetraploids to provide resistance to X. campestris pv. zinniae.

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Miyajima, Daiichiro. "Causes of Low Double-flowered Seed Production in Breeding Zinnia." Journal of the American Society for Horticultural Science 120, no. 5 (1995): 759–64. http://dx.doi.org/10.21273/jashs.120.5.759.

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The causes of low production of seeds capable of producing double-flowered plants and of high production of seeds capable of producing single-flowered plants were investigated in zinnias (Zinnia violaceu Cav.). Poor pollination was a major cause of the low seed set. A tubular floret produced abundant pollen; however, the pollen flow to ray stigmas was limited due to the infrequent visitation by pollinators. Moreover, in the double-flowered capitula, newly opened ray petals overlapped on the pistils that unfolded the previous day. These phenomena were considered to cause low seed set in double-flowered plants. Actually, capitula with more tubular florets produced more seeds than those with fewer tubular florets. Pollen germination and plants near zinnias had additional possible influences on seed production of double-flowered zinnias.

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Myung, I. S., J. Y. Lee, H. L. Yoo, J. M. Wu, and H. S. Shim. "Bacterial Leaf Spot of Zinnia Caused by Xanthomonas campestris pv. zinniae, a New Disease in Korea." Plant Disease 96, no. 7 (2012): 1064. http://dx.doi.org/10.1094/pdis-03-12-0319-pdn.

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In September 2011, bacterial leaf spot was observed on zinnia plants (Zinnia elegans L.) grown in a garden in Suwon, Korea. Leaf symptoms included angular lesions that were yellow or brown-to-reddish brown in the center. Bacterial isolates (BC3293 to BC3299) were recovered on trypticase soy agar from lesions surface-sterilized in 70% ethyl alcohol for 1 min. Pathogenicity of the isolates was confirmed by spray inoculation with a bacterial suspension (106 CFU/ml) prepared in sterile distilled water and applied to zinnia plants at the four- to five-leaf growth stage (two plants per isolate). Sterile distilled water was used as the negative control. The inoculated plants were incubated in a greenhouse at 26 to 30°C and 95% relative humidity. Characteristic leaf spot symptoms developed on inoculated zinnia plants 5 days after inoculation. No symptoms were observed on the negative control plants. The bacterium reisolated from the inoculated leaves was confirmed through gyrB gene sequence analysis (3). All isolates were gram-negative, aerobic rods, each with a single flagellum. Isolates were positive for catalase and negative for oxidase. The biochemical and physiological tests for differentiation of Xanthomonas were performed using methods described by Shaad et al. (2). The isolates were positive for mucoid growth on yeast extract-dextrose-calcium carbonate agar, growth at 35°C, hydrolysis of starch and esculin, protein digestion, acid production from arabitol, and utilization of glycerol and melibiose. Colonies were negative for ice nucleation, and alkaline in litmus milk. The gyrB gene (870 bp) and the 16S-23S rRNA internal transcribed spacer (ITS) regions (884 bp) were sequenced to aid in identification of the original field isolates using published PCR primer sets Xgyr1BF/Xgyr1BR (3) and A1/B1 (1), respectively. Sequence of the gyrB gene (GenBank Accession Nos. JQ665732 to JQ665738) from the zinnia field isolates shared 100% sequence identity with the reference strain of Xanthomonas campestris pv. zinniae (GenBank Accession No. EU285210), and the ITS sequences (GenBank Accession Nos. JQ665725 to JQ665731) had 99.9% sequence identity with X. campestris pv. zinnia XCZ-1 (GenBank Accession No. EF514223). On the basis of the pathogenicity assays, biochemical and physiological tests, and sequence analyses, the isolates were identified as X. campestris pv. zinniae. To our knowledge, this is the first report of bacterial leaf spot of zinnia caused by X. campestris pv. zinniae in Korea. The disease is expected to result in economic and aesthetic losses to plants in Korean landscapes. Thus, seed treatment with bactericides will be required to control the bacterial leaf spot of zinnia before planting. References: (1) T. Barry et al. The PCR Methods Appl. 1:51, 1991. (2) N. W. Schaad et al. Page 189 in: Laboratory Guide for Identification of Plant Pathogenic Bacteria. 3rd ed. N. W. Schaad et al., eds. The American Phytopathological Society, St. Paul, MN, 2001. (3) J. M. Young et al. Syst. Appl. Microbiol. 31:366, 2008.

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Łacicowa, Barbara, Antoni Filipowicz, and Anna Wagner. "Fungi pathogenic for Zinnia elegans L." Acta Mycologica 15, no. 1 (2014): 11–20. http://dx.doi.org/10.5586/am.1979.002.

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Among fungi isolated from specimens of <i>Zinnia elegans</i> L. dying due to rotting of the stem base and root neck the most frequent were <i>Sclerotinia sclerotiorum, Fusarium culmorum, F. solani, F. oxysporum</i> and <i>Alternaria zinniae. Alternaria zinniae</i> has been found to very harmful to these plants. The fungus harmed the root neck and stem base and caused formation of spots on above-ground organs, especially on leaves. <i>Sclerotinia sclerotiorum</i> and <i>Fusarium culmorum</i> also proved to be very harmful, especially for seedlings.

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Gombert, Linda, Susan Hamilton, and Mark Windham. "Evaluation of Disease Resistance among 57 Varieties of Zinnia elegans." HortScience 33, no. 3 (1998): 467a—467. http://dx.doi.org/10.21273/hortsci.33.3.467a.

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Fifty-seven of the most widely grown, commercially popular varieties of Zinnia elegans were evaluated for disease susceptibility under uniform field conditions. Plants were started from seed and transplanted into cell-packs to be grown on as bedding plants. They were later transplanted into the field and observed for development and progression of the diseases alternaria blight (Alternaria zinniae), powdery mildew (Erisyphe cichoracearum), and bacterial leaf and flower spot (Xanthomonas campestris pv. zinniae). Evaluations were performed throughout the growing season in order to rate each variety on its susceptibility to disease based upon severity of infection as well as portion of plant affected. Results will be presented on disease susceptibility and resistance of the 57 varieties evaluated.

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Miyajima, Daiichiro. "Improvement of Ornamental Value by Seed Selection in Double-flowered Zinnias." HortScience 33, no. 4 (1998): 696–98. http://dx.doi.org/10.21273/hortsci.33.4.696.

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In double-flowered (Dbf) zinnias (Zinnia violacea Cav.), seed lots inevitably contain seeds for single-flowered (Sgf) plants. A Sgf capitulum is composed of many disk florets and some ray florets with wide ovaries. A Dbf capitulum is composed of many ray florets with ovaries of various widths. Based on differences in morphology of florets that develop in Sgf and Dbf capitula and the fact that doubling is a genetically controlled trait, seeds of two cultivars of Dbf zinnias were classified into three groups by morphology of the pericarps: thin (RT) and wide (RW) seeds (achenes) produced by ray florets, and seeds (D) produced by disk florets. Plants were grown from these seeds and the ornamental value of their capitula was evaluated. Percentage of plants with Dbf capitula and the number of ray florets in a capitulum were highest for plants from RT seeds. Thus, the ornamental value of Dbf zinnias could be heightened by selecting RT seeds.

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Dudley, Jerry B., Alton J. Pertuit, and Joe E. Toler. "Leonardite Influences Zinnia and Marigold Growth." HortScience 39, no. 2 (2004): 251–55. http://dx.doi.org/10.21273/hortsci.39.2.251.

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The addition of leonardite may increase, or at least maintain, production quality of ornamental plants and permit reductions in fertilizer inputs. The objective of this study was to determine the effects of a Utah-mined leonardite on early stages of zinnia (Zinnia elegans Jacq. `Small World Pink') and marigold (Tagetes patula L. `Janie Yellow') growth. The Utah leonardite was characterized by comparing it to the International Humic Substances Society's leonardite standard. Zinnia and marigold seedlings and transplants were grown in sand and 1 sand: 1 peat media (by volume) with leonardite additions of 0%, 3.125%, 6.25%, and 12.5%. Both species showed positive growth responses to 3.125% leonardite in each medium compared to fertilizer alone. Plant responses to increased leonardite additions were generally quadratic, and optimal leonardite levels were estimated. For growing zinnias, optimal conditions were determined to be 7.5% leonardite in a sand medium for seedlings and 8% in a sand-peat mixture for transplants. A sand-peat medium containing 7% leonardite was determined to be optimal for growing marigold seedlings and transplants. Addition of leonardite to growing medium offers promise for reducing fertilizer use during production of some ornamental plants.

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Dissertations / Theses on the topic "Zinnion"

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Veenker, Hermannus Johannes Jacobus Maria. "De zinnen verzetten." [S.l. : [Groningen] : s.n.] ; [University Library Groningen] [Host], 1996. http://irs.ub.rug.nl/ppn/152777180.

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Thelan, Michael Paul. "Differentiation-specific nuclease of Zinnia elegans." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.316002.

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Montillet, Jean-Luc. "Dosage radioimmunologique du zinniol application à l'étude de cette toxine dans l'alternariose de la carotte." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37599747t.

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Montillet, Jean-Luc. "Dosage radioimmunologique du zinniol : application a l'etude de cette toxine dans l'alternariose de la carotte." Toulouse 3, 1986. http://www.theses.fr/1986TOU30208.

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Un dosage radioimmunologique specifique du zinniol a ete au point; les etapes de ce travail ont ete les suivantes: - synthese d'une molecule immunogene (conjugue zinniol-proteine porteuse). - obtention d'anticorps specifique (4 ci/mmole). - mise au point du dosage radioimmunologique valide du point de vue de sa specificite, de sa reproductibilite et de sa sensibilite (limite de detection 0,14 nn/essai). Cet outil a permis de realiser des dosages sur des plantes infectees. Ces resultats inedits montrent que la molecule est emise tres rapidement dans les tissus infectes (12 h apres inoculation).

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Withaar, Rienk Gerwin. "The role of the phonological loop in sentence comprehension." [S.l. : Groningen : s.n. ; University Library Groningen] [Host], 2002. http://irs.ub.rug.nl/ppn/303542071.

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Mourelatou, Maria. "Proliferation versus differentiation in the Zinnia elegans model system." Thesis, University of East Anglia, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.393124.

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Lin, Quan. "Differentiation of tracheary elements from mesophyll cells of Zinnia elegens L." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358693.

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Driel, Joost van. "Prikkeling der zinnen : de stilistische diversiteit van de Middelnederlandse epische po·ezie." Zutphen Walburg Pers, 2007. http://digitool.hbz-nrw.de:1801/webclient/DeliveryManager?pid=2603801&customa̲tt2̲=simplev̲iewer.

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Thuleau, Patrice. "Le canal calcium chez Daucus carota L : caractérisation biochimique et régulation du fonctionnement par une phytotoxine d'origine fongique, le zinniol." Toulouse 3, 1990. http://www.theses.fr/1990TOU30173.

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Le recepteur des antagonistes des canaux calcium chez daucus carota, solubilise a partir des membranes par le chaps, a ete purifie par chromatographie d'affinite sur lectines greffees et d'echanges d'ions avec un taux de purification de 36,5 et un rendement de 30%. L'analyse en electrophorese de l'extrait denature fait apparaitre quatre polypeptides majeurs de 75, 66, 32 et 16 kda. Le photomarquage in situ ou apres solubilisation, a l'aide d'un ligand specifique photoactivable, a permis d'identifier un polypeptide de 75 kda, la proteine native presentant un poids moleculaire identique. La double localisation sur le plasmalemme et le tonoplaste, suggere un role potentiel du recepteur dans la perception de signaux extra ou intracellulaires. Ainsi le zinniol, phytotoxine produite par alternaria dauci en se fixant sur des sites specifiques, partiellement communs avec ceux des antagonistes des canaux calcium, stimule de maniere dose-dependante l'entree de calcium dans des protoplastes de carotte. Cet effet est inhibe par les antagonistes. Chez une lignee resistante a la toxine, le zinniol, se fixant a des taux negligeables, ne provoque aucun effet sur les influx de calcium. Le site primaire d'action de la molecule pourrait donc etre un recepteur, commun avec les antagonistes, lie au canal calcium dont le fonctionnement est alors perturbe

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Serk, Henrik. "Cellular Aspects of Lignin Biosynthesis in Xylem Vessels of Zinnia and Arabidopsis." Doctoral thesis, Umeå universitet, Institutionen för fysiologisk botanik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-109179.

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Lignin is the second most abundant biopolymer on earth and is found in the wood (xylem) of vascular land plants. To transport the hydro-mineral sap, xylem forms specialized conduit cells, called tracheary elements (TEs), which are hollow dead cylinders reinforced with lateral secondary cell walls (SCW). These SCWs incorporate lignin to gain mechanical strength, water impermeability and resistance against pathogens. The aim of this thesis is to understand the spatio-temporal deposition of lignin during TE differentiation and the relationship with its neighbouring cells. In vitro TE differentiating cell cultures of Zinnia elegans and Arabidopsis thaliana are ideal tools to study this process: cells differentiate simultaneously into 30-50% TEs while the rest remain parenchymatic (non-TEs). Live-cell imaging of such TEs indicated that lignification occurs after programmed cell death (PCD), in a non-cell autonomous manner, in which the non-TEs provide the lignin monomers. This thesis confirms that lignification occurs and continues long after TE PCD in both in vitro TE cultures and whole plants using biochemical, pharmacological and cytological methods. The cooperative supply of lignin monomers by the non-TEs was demonstrated by using Zinnia and Arabidopsis in vitro TE cultures. Inhibitor experiments revealed further that the non-TEs supply reactive oxygen species (ROS) to TEs and that ROS are required for TE post-mortem lignification. Characterization of the non-TEs showed an enlarged nucleus with increased DNA content, thus indicating that non-TEs are in fact endoreplicated xylem parenchyma cells (XP). The cooperative lignification was confirmed in whole plants by using knock-out mutants in a lignin monomer synthesis gene, which exhibit reduced TE lignification. The XP specific complementation of these mutants led to nearly completely rescuing the TE lignin reduction. Using microscopic techniques, the spatial distribution of lignin was analyzed in TEs from in vitro cultures and whole plants, revealing that lignification is restricted to TE SCWs in both protoxylem and metaxylem. These specific deposition domains were established by phenoloxidases, i.e. laccases localized to SCWs and peroxidases, present in SCWs and the apoplastic space. Laccases were cell-autonomously produced by developing TEs, indicating that the deposition domains are defined before PCD. Altogether, these results highlight that the hydro-mineral sap transport through TEs is enabled by the spatially and temporally controlled lignification of the SCW. Lignification occurs post-mortem by the supply of monomers and ROS from neighbouring XP cells and is restricted to specific deposition domains, defined by the pre-mortem sequestration of phenoloxidases.

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Books on the topic "Zinnion"

1

Quick, Amanda. Zinnia. Beeler Large Print, 1997.

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Quick, Amanda. Zinnia. Pocket Star Books, 1997.

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Alison's zinnia. Greenwillow Books, 1990.

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Zinnia and Dot. Viking, 1992.

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De zeven laatste zinnen. Contact, 2010.

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Virahsawmy, Dev. Morisien, Zinnia, Ziliet ek lezot. Educational Production Ltd., 2001.

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Huriet, Geneviève. Aunt Zinnia and the Ogre. Gareth Stevens Children's Books, 1992.

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Polette, Nancy. Apple trees to zinnias: Research reporting patterns. Book Lures, 1992.

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Lemaire, Ton. Met open zinnen: Natuur, landschap, aarde. 3rd ed. Ambo, 2002.

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Beheydt, L. Een Zinnig woord: Werkboek elementaire woordenschat. Van In, 1989.

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Book chapters on the topic "Zinnion"

1

Sastry, K. Subramanya, Bikash Mandal, John Hammond, S. W. Scott, and R. W. Briddon. "Zinnia spp. (Zinnia)." In Encyclopedia of Plant Viruses and Viroids. Springer India, 2019. http://dx.doi.org/10.1007/978-81-322-3912-3_1029.

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Neuenschwander, Eduard. "Zürichs Zinnen." In Niemandsland. Birkhäuser Basel, 1988. http://dx.doi.org/10.1007/978-3-0348-6660-6_26.

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Azimova, Shakhnoza S., and Anna I. Glushenkova. "Zinnia elegans Jacq." In Lipids, Lipophilic Components and Essential Oils from Plant Sources. Springer London, 2012. http://dx.doi.org/10.1007/978-0-85729-323-7_472.

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Smith, M. A. L. "Micropropagation of Zinnia." In Biotechnology in Agriculture and Forestry. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-662-03354-8_22.

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Szopińska, Dorota. "Diseases of Zinnia." In Handbook of Plant Disease Management. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-32374-9_28-1.

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Szopińska, Dorota. "Diseases of Zinnia." In Handbook of Plant Disease Management. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-39670-5_28.

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Onrust, Margreet, Arie Verhagen, and Rob Doeve. "Het schikken van zinnen." In Formuleren. Bohn Stafleu van Loghum, 1993. http://dx.doi.org/10.1007/978-90-313-9474-6_7.

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Stieve, S. M., and D. P. Stimart. "Somaclonal Variation in Zinnia." In Biotechnology in Agriculture and Forestry. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61081-3_24.

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Sugiyama, Munetaka, and Hiroo Fukuda. "Zinnia mesophyll culture system to study xylogenesis." In Plant Tissue Culture Manual. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0103-2_55.

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Sugiyama, Munetaka, and Hiroo Fukuda. "Zinnia mesophyll culture system to study xylogenesis." In Plant Tissue Culture Manual. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0303-9_5.

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Conference papers on the topic "Zinnion"

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Mohamed, Marina, Nazihah Ismail, Syafiza Saila Samsudin, and Noor Azimah Ibrahim. "Mathematical nature’s pattern in Zinnia Peruviana." In PROCEEDING OF THE 25TH NATIONAL SYMPOSIUM ON MATHEMATICAL SCIENCES (SKSM25): Mathematical Sciences as the Core of Intellectual Excellence. Author(s), 2018. http://dx.doi.org/10.1063/1.5041579.

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Fladila, Qisthi, and Maryani. "Anatomical responses of Zinnia violacea Cav. roots and stems to batik wastewater." In THE 6TH INTERNATIONAL CONFERENCE ON BIOLOGICAL SCIENCE ICBS 2019: “Biodiversity as a Cornerstone for Embracing Future Humanity”. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0015760.

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Maryani, Ninda Nur Amalia, and Tevi Agustina. "Batik liquid waste inhibited germination and degraded root tissues of Tagetes erecta L. and Zinnia violacea Cav." In THE 6TH INTERNATIONAL CONFERENCE ON BIOLOGICAL SCIENCE ICBS 2019: “Biodiversity as a Cornerstone for Embracing Future Humanity”. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0015768.

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Tugbaeva, A. S., A. A. Ermoshin, and I. S. Kiseleva. "Sodium chloride affects the growth, tissue organization of axial organs andlignification of the cell walls of plants of Zinnia elegans Jacq." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-442.

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Ibragimova, C. M., E. A. Trifonova, E. A. Filipenko, and A. V. Kochetov. "STUDY OF THE ROLE OF EXTRACELLULAR RIBONUCLEASES IN PHYTOPATHOGENESIS IN PLANTS BY THE EXAMPLE OF TRANSGENIC POTATO PLANTS CARRIED WITH THE GENES OF ZRNaseII EXTRACELLULAR RIBONUCLEASIS OF ZINNIA." In The All-Russian Scientific Conference with International Participation and Schools of Young Scientists "Mechanisms of resistance of plants and microorganisms to unfavorable environmental". SIPPB SB RAS, 2018. http://dx.doi.org/10.31255/978-5-94797-319-8-913-916.

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Reports on the topic "Zinnion"

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Eriksson, Karl-Erik L., and Jeffrey F. D. Dean. Mechanisms of Lignin Biosynthesis During Xylogenesis in Zinnia elegans. Final report. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/762053.

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Warker, Peter M. Strategic Leadership Competency Development: A Comparison of Generals Zinni and Powell. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada432492.

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Eriksson, K. E. L., and J. F. D. Dean. Mechanisms of lignin biosynthesis during xylogenesis in Zinnia elegans. Final report, July 1, 1992--June 30, 1996. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/477719.

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