<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1405-2768</journal-id>
<journal-title><![CDATA[Polibotánica]]></journal-title>
<abbrev-journal-title><![CDATA[Polibotánica]]></abbrev-journal-title>
<issn>1405-2768</issn>
<publisher>
<publisher-name><![CDATA[Instituto Politécnico Nacional, Escuela Nacional de Ciencias Biológicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-27682022000200123</article-id>
<article-id pub-id-type="doi">10.18387/polibotanica.54.8</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Germinación y multiplicación de plantas in vitro de Heimia salicifolia (Lythraceae).]]></article-title>
<article-title xml:lang="en"><![CDATA[Germination and micropropagation in vitro of Heimia salicifolia (Lythraceae).]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ordoñez Posadas]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martínez-Cárdenas]]></surname>
<given-names><![CDATA[M. de L.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez de la O]]></surname>
<given-names><![CDATA[J.L.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Autónoma Metropolitana División de Ciencias Biológicas y de la Salud ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Autónoma de Chapingo Área de Fitotecnia ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2022</year>
</pub-date>
<numero>54</numero>
<fpage>123</fpage>
<lpage>138</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-27682022000200123&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-27682022000200123&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-27682022000200123&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Las técnicas de germinación y micropropagación in vitro permiten rescatar y multiplicar plantas a gran escala, permitiendo la evaluación del mejor protocolo de cultivo, lo que resulta en su optimización. La técnica de germinación para Heimia salicifolia se planteó a partir del empleo de concentraciones diferentes de citocininas y giberelinas (Tabla 1) en medio MS al 100% suplementados con 3% sacarosa, evaluando los efectos de estos reguladores de crecimiento sobre tiempos de germinación y desarrollo vegetal acorde a número de hojas, tamaño promedio de las vitroplantas por tratamiento y vigor. No se presentó diferencia significativa entre los tratamientos (Tabla 1), sin embargo, la evaluación de las plántulas transcurridos cuatro meses, permite concluir que los reguladores de crecimiento presentes desde la germinación producen afectaciones a la calidad de las plántulas. La micropropagación llevada a cabo con medio básico (Murashige &amp; Skoog, 1962) al 100%, con diferentes concentraciones de 2-isopentiladenina (2iP), Bencilaminopurina (BA) y Kinetina (K), suplementados con 30g/L&#8722;1 de sacarosa, 100 mg L&#8722;1 de Mioinositol, 0.40mg L&#8722;1 de Tiamina, 60 mg L&#8722;1 de L-cisteína y pH de 5.7± 0.1. Los resultados del protocolo exhibieron diferencias significativas a partir de la obtención de explantes basales y apicales. El tratamiento 2 (0.3 mg L&#8722;1 para 2iP, BA y Kinetina) mostró resultados diferenciales en cuanto a número de brotes y número de hojas, sin embargo, el crecimiento longitudinal o tamaño promedio diferencial de la plántula se obtuvo a partir del tratamiento sin hormonas, resultando estos dos tratamientos como eficaces para la micropropagación de Heimia salicifolia.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract In vitro germination and micropropagation techniques allow to rescue and propagate plants on a large scale. The present work evaluated different cultivation treatments to determine the optimal micropropagation protocol. It is possible to establish an in vitro protocol for optimal germination and cloning of Heimia salicifolia based on the requirements for germination and propagation in situ.Germination protocol was applied at different concentrations of cytokinins and gibberellins in MS medium (1962) at 100% with 3% sucrose (Table 1), but the variables obtained by the different treatments allow to conclude that the best method for germination was without vitamins reducing the cost and obtaining the same results. The effect of these growth regulators on germination time and plant development for four months was evaluated according to the number of leaves, length in centimeters and vigor of seedlings. There were significant differences between the treatments in all the variables, concluding that the best treatment for germination and maintenance of vitroplants is without hormones.For micropropagation protocol was necessary the evaluation of 100% MS medium with different concentrations of 2ip, BA and Kinetin, supplemented with 30 g L-1 of sucrose, 100 mg L-1 of Myo-inositol, 0.40 mg of Thiamine, 60 mg L-1 of L-cysteine and pH of 5.7 ± 0.1. (Table 3). There were significant differences between basal and apical explants. Treatment 2 (0.3 mg L-1 2ip, BA and Kinetin) showed the best results in terms of number of shoots and number of leaves. However, the best results in longitudinal growth of the seedlings were obtained with the treatment without hormones. These two treatments showed to be effective for micropropagation allowing to conclude that it is possible to establish a micropropagation protocol for Heimia salicifolia from apical and basal explants with exponential growth.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Cultivo in vitro]]></kwd>
<kwd lng="es"><![CDATA[giberelinas]]></kwd>
<kwd lng="es"><![CDATA[citocininas]]></kwd>
<kwd lng="es"><![CDATA[germinación]]></kwd>
<kwd lng="es"><![CDATA[micropropagación]]></kwd>
<kwd lng="en"><![CDATA[In vitro culture]]></kwd>
<kwd lng="en"><![CDATA[gibberellins]]></kwd>
<kwd lng="en"><![CDATA[cytokinins]]></kwd>
<kwd lng="en"><![CDATA[germination]]></kwd>
<kwd lng="en"><![CDATA[micropropagation]]></kwd>
</kwd-group>
</article-meta>
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