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Journal articles on the topic 'Tigridia pavonia'

Author: Grafiati
Published: 11 September 2021
Last updated: 18 February 2022

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1

Leszczyñska-Borys, H., M. W. Borys, and M. T. Borys. "Algunas características de la tigridia Tigridia pavonia Ker. Gawl." Revista Chapingo Serie Horticultura I, no. 04 (April 1995): 117–30. http://dx.doi.org/10.5154/r.rchsh.1995.03.017.

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2

RODRÍGUEZ, AARÓN, DENNIS SZESZKO, and GUADALUPE MUNGUÍA-LINO. "The species of Tigrideae (Iridaceae) in the Sierra of Nanchititla, State of México, Mexico, and description of the new species Tigridia nanchititlensis." Phytotaxa 446, no. 5 (June 3, 2020): 268–80. http://dx.doi.org/10.11646/phytotaxa.446.5.1.

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The Sierra of Nanchititla Natural Park is located in central Mexico. It occupies the southwestern corner of the State of México, within the municipality of Luvianos at the border with the states of Michoacán and Guerrero. It is part of the Balsas Basin biogeographical province. The sierra is a topographically complex region, isolated from the neighboring sierras, harboring several endemic species. Here, Tigridia nanchititlensis is described and illustrated as a new species. Morphologically, this taxon pertains to the subgenus Hydrotaenia. It is a rupicolous and pendulous plant characterized by its horizontal flowers and upright fruits. It is most closely related to T. meleagris, and co-occurs in the studied area with other species of Tigrideae, such as Cardiostigma longispatha, Cipura campanulata, Tigridia meleagris, T. mortonii, and T. pavonia. Two of them, Tigridia nanchititlensis and T. mortonii are endemic to the Sierra of Nanchititla.
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3

Effers, Kerstin, Bettina Scholz, Christoph Nickel, Bernadette Hanisch, and Franz-Josef Marner. "ChemInform Abstract: Structure Determination of Tigridial, an Iridopentaene from Tigridia pavonia (Iridaceae)." ChemInform 31, no. 6 (June 11, 2010): no. http://dx.doi.org/10.1002/chin.200006194.

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4

Carrillo-Ocampo, Aída, and E. M. Engleman. "Anatomía de la semilla de Tigridia pavonia (Iridaceae)." Botanical Sciences, no. 70 (May 31, 2017): 66. http://dx.doi.org/10.17129/botsci.1655.

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With methods of light microscopy, histochemical staining and scanning electron microscopy, it was found that the ovule in the seed of Tigridia pavonia (Iridaceae) is anatropous, bitegmic, and crassinucellate. During development, the exotegmen is crushed and the endotegmen persists with tannins in the lumens and in the walls, which also react positively for lignin. The exotesta contains tannins and its outer walls are convex, thickened, and cuticularized. The mesotesta has multiple layers, accumulates abundant lipids, and forms a bulge in the chalaza. The cell walls of the endotesta collapse and accumulate tannins. In the chalaza, a hypostasal cushion contains tannins in the lumens and in the walls, which also react positively for lignin. At the micropylar end of the seed there is an operculum which consists of: a) a slightly crushed exotegmen, b) an endotegmen with cuticular thickenings that are concentric with respect to the micropyle, c) hemispherical deposists of cutin on the anticlinal walls of the endotegmen, and c) a thin layer of endosperm that covers the radicle. During its cellular stage of development, the endosperm has conspicuous transfer walls at the chalazal end next to the nucella. The embryo is small and has a conical cotyledon.
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5

Borys, M. W., H. Leszczyñska-Borys, and J. L. Galván. "EMERGENCIA Y CRECIMIENTO CONTÍNUO DE RAÍCES DE Tigridia pavonia Ker. Gawl." Revista Chapingo Serie Horticultura VI, no. 01 (June 2000): 57–61. http://dx.doi.org/10.5154/r.rchsh.1998.11.072.

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6

Piña-Escutia, J. L., L. M. Vázquez-García, and A. M. Arzate-Fernández. "Interspecific hybridization between Tigridia pavonia and T. augusta through ovary slice culture." Genetics and Molecular Research 12, no. 1 (2013): 15–22. http://dx.doi.org/10.4238/2013.january.16.4.

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7

Tapia-Pastrana, Fernando, and Fernando Tapia-Aguirre. "Evidencia de autopoliploidía y translocaciones en el cariotipo de Tigridia pavonia (Iridaceae, Iridoideae) de la Reserva Ecológica del Pedregal de San Ángel, México." Acta Botanica Mexicana, no. 121 (October 2, 2017): 151–58. http://dx.doi.org/10.21829/abm121.2017.1205.

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Antecedentes y Objetivos: Tigridia pavonia fue propuesto como un taxon alotetraploide 2n=4x=28, pero sin evidencia citogenética que sustente su origen híbrido. Es una especie de amplia distribución en México y sus poblaciones carecen de una fórmula cariotípica y un análisis detallado de los cromosomas con satélites como criterio para determinar el número de organizadores nucleolares que confirmen o no dominancia nucleolar. En este trabajo se analiza y describe el número y arquitectura cromosómica de T. pavonia de una población mexicana, en búsqueda de evidencias que soporten o descarten su origen híbrido y se propone una fórmula cariotípica acorde al nivel y origen de ploidía.Métodos: Se utilizó una técnica de extendido en superficie y secado al aire que incluye maceración enzimática y choque hipotónico en meristemos radiculares para obtener los cromosomas en mitosis de seis individuos de T. pavonia, nativa de la Reserva Ecológica del Pedregal de San Ángel, en la Ciudad de México.Resultados clave: Se confirmó un cariotipo bimodal con 28 cromosomas que, de acuerdo a su similitud morfológica, fueron incluidos en siete grupos de cuatro cromosomas homólogos cada uno. Los cromosomas del grupo más pequeño exhibieron constricciones secundarias asociadas a macrosatélites lo que evidenció ausencia de dominancia nucleolar o amfiplastía diferencial. En el grupo de cromosomas grandes se observaron configuraciones que sugieren rearreglos por translocaciones. Se propone la fórmula 6m + 8sm para el cariotipo haploide.Conclusiones: Citogenéticamente, la presencia de cuatro satélites descarta un origen alotetraploide y la evidencia de posibles translocaciones se correlaciona con fragmentos, cromosomas B y centrómeros frágiles observados en otras especies del género. Lo anterior apoya el papel activo de las translocaciones en la conformación del cariotipo bimodal de T. pavonia.
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8

Kumar, Lekha, Sincy Joseph, and Narmatha Bai. "Micropropagation of Tigridia pavonia (L.f) DC-a potential floricultural plant from twin scale explants." Asian Pacific Journal of Reproduction 1, no. 1 (March 2012): 38–41. http://dx.doi.org/10.1016/s2305-0500(13)60045-7.

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9

Díaz-L., E., J. Pichardo-R., E. De la Cruz-T., T. Norman-M., F. Sandoval-R, and L. Vázquez-G. "VARIABILIDAD INDUCIDA EN Tigridia pavonia (L. f.) D.C. var. Sandra POR IRRADIACIÓN DE BULBOS CON RAYOS GAMMA DE 60Co." Revista Chapingo Serie Horticultura IX, no. 02 (December 2003): 235–37. http://dx.doi.org/10.5154/r.rchsh.2002.06.037.

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10

Arroyo-Martínez, Hugo Abelardo, Amaury Martín Arzate-Fernández, Rodrigo Barba-González, and José Luis Piña-Escutia. "Karyotype analysis and physical mapping of the 5S and 45S rDNA genes in Tigridia pavonia var. Dulce (Iridaceae)." Caryologia 71, no. 1 (November 15, 2017): 1–6. http://dx.doi.org/10.1080/00087114.2017.1382302.

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11

Leonel, Hugo F., and Gloria C. Luna-Cabrera. "Evaluación de Procesos Participativos para la Formación Ambiental a partir del Conocimiento de Watsimba Tigridia pavonia (L.F.) DC. en Sibundoy, Putumayo, Colombia." Información tecnológica 28, no. 1 (2017): 219–28. http://dx.doi.org/10.4067/s0718-07642017000100022.

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12

Effers, Kerstin, Bettina Scholz, Christoph Nickel, Bernadette Hanisch, and Franz-Josef Marner. "Structure Determination of Tigridial, an Iridopentaene fromTigridia pavonia (Iridaceae)." European Journal of Organic Chemistry 1999, no. 11 (November 1999): 2793–97. http://dx.doi.org/10.1002/(sici)1099-0690(199911)1999:11<2793::aid-ejoc2793>3.0.co;2-z.

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13

Arzate-Fernández, Amaury Martín, José Luis Piña-Escutia, and Luis Miguel Vázquez-García. "In vitro regeneration and genetic fidelity of Tigridia pavonia (L.f.) DC." Electronic Journal of Biotechnology 13, no. 1 (January 15, 2010). http://dx.doi.org/10.2225/vol13-issue1-fulltext-1.

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14

Piña-Escutia, José Luis, Luis Miguel Vázquez-García, and Amaury Martín Arzate-Fernández. "Variety discrimination of Tigridia pavonia (L.f.) DC. assesed by different length RAPD primers." Electronic Journal of Biotechnology 13, no. 4 (June 15, 2010). http://dx.doi.org/10.2225/vol13-issue4-fulltext-7.

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15

Saddler, G. S. "Burkholderia gladioli pv. gladioli. [Descriptions of Fungi and Bacteria]." IMI Descriptions of Fungi and Bacteria, no. 122 (July 1, 1994). http://dx.doi.org/10.1079/dfb/20056401218.

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Abstract A description is provided for Burkholderia gladioli pv. gladioli. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Crocus spp., Freesia hybrida, F. refracta, Gladiolus colvillei, G. hortulanus, Iris spp., Ixia maculata and Tigridia pavonia. In addition the same organism has been reported to infect various ferns, including Asplenium nidus, Platycerium bifurcatum, Pteris cretica, P. ensiformis, Adiantum sp., Cyrtomium falcatum, Davallia fejeensis, Pelleae rotundifolia (63, 3386; 64, 216). Orchids of the genus Dendrobium are also thought to be susceptible (63, 5459). DISEASE: Rot of stem bases and corms of gladioli; leaf spots and blight of ferns. Leaves begin dying at the tip, initially spots are reddish in colour becoming enlarged and circular and darkening to dark brown to black. Yellow or orange sunken spots develop on the corm. Severity of the disease may be enhanced by the actions of the root knot nematode, Meloidogyne javanica (53, 3055), bulb mites and possibly grub and wireworm injury. Young tissue appears to be the most susceptible. GEOGRAPHICAL DISTRIBUTION: South Africa, Zimbabwe, China, Japan, Thailand, Australia (NT, NSW, Qd., S. Aust., Tas., WA, Vict.), New Caledonia, Belgium, Czechoslovakia, Finland, Germany, Italy, Netherlands, Romania, USA (widespread), Canada (Ontario, British Columbia), Argentina. TRANSMISSION: By the movement of infected corms.
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