<?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>2007-4298</journal-id>
<journal-title><![CDATA[Botanical Sciences]]></journal-title>
<abbrev-journal-title><![CDATA[Bot. sci]]></abbrev-journal-title>
<issn>2007-4298</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Botánica de México A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2007-42982024000200464</article-id>
<article-id pub-id-type="doi">10.17129/botsci.3415</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Corolla micromorphology in 12 plant species with different pollination systems]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vélez-Esperilla]]></surname>
<given-names><![CDATA[Fernando]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fondón-Aguilar]]></surname>
<given-names><![CDATA[Ángela]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez-Riaño]]></surname>
<given-names><![CDATA[Tomás]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ortega-Olivencia]]></surname>
<given-names><![CDATA[Ana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Extremadura Facultad de Ciencias Departamento de Biología Vegetal, Ecología y Ciencias de la Tierra]]></institution>
<addr-line><![CDATA[ Badajoz]]></addr-line>
<country>Spain</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Kyoto University Graduate School of Science Department of Botany]]></institution>
<addr-line><![CDATA[ Kyoto]]></addr-line>
<country>Japan</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2024</year>
</pub-date>
<volume>102</volume>
<numero>2</numero>
<fpage>464</fpage>
<lpage>481</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2007-42982024000200464&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2007-42982024000200464&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2007-42982024000200464&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Background: Floral microstructure, with multiple functions, is very important in pollination biology.  Questions:  Are the expected general characteristics of corolla micromorphology fulfilled in the selected species with different pollination systems?  Studied species: Agave americana, Arbutus unedo, Aristolochia paucinervis, Cestrum nocturnum, Cytinus hypocistis subsp. macranthus, C. ruber, Dianthus lusitanus, Grevillea robusta, Musa x paradisiaca, Nicotiana glauca, Stellaria media and Teucrium fruticans.  Study site and dates: Southern Spain, 2017-2019.  Methods: Floral micromorphological characters were studied by light and scanning electron microscopy and analyzed using different statistical tests.  Results:  The adaxial side of the corolla lobes in melittophilous, myrmecophilous, psychophilous and sapromyophilous species showed papillose cells, and the same was true of the sphingophilous species Cestrum nocturnum and hummingbird-pollinated Nicotiana glauca. In contrast, tabular cells were observed in the perching-pollinator ornithophilous species Grevillea robusta, the two studied chiropterophilous species, and autogamous Stellaria media. In addition, corolla mesophyll was thicker in chiropterophilous species. Furthermore, differences were detected in cell turgidity (in protogynous Aristolochia paucinervis) and in mesophyll thickness between male and female flowers (Cytinus).  Conclusions:  Papillose cells were present in corollas in physical contact with pollinators, as expected, but also appeared in corollas of some other species without such contact. We recommend that studies of dichogamous and unisexual species include comparisons of corolla micromorphology between sexual states, as differences may exist in cell turgidity or mesophyll thickness. We also caution against the widespread view that certain types of pollinators do not mechanically interact with the epidermal surface of the corolla.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Antecedentes: La microestructura floral posee gran importancia en biología de la polinización, con múltiples funciones.  Preguntas: ¿Se cumplen los patrones esperados de micromorfología de la corola en las especies seleccionadas?  Especies de estudio: Agave americana, Arbutus unedo, Aristolochia paucinervis, Cestrum nocturnum, Cytinus hypocistis subsp. macranthus, C. ruber, Dianthus lusitanus, Grevillea robusta, Musa x paradisiaca, Nicotiana glauca, Stellaria media y Teucrium fruticans.  Sitio y años de estudio:  Sur de España, 2017-2019.  Métodos:  Micromorfología floral estudiada a MO y MEB y analizada mediante pruebas estadísticas.  Resultados:  La cara adaxial de los lóbulos corolinos en las especies melitófilas, mirmecófilas, psicófilas y sapromófilas mostró células papilosas, pero también en la esfingófila Cestrum nocturnum y en la ornitófila por colibríes Nicotiana glauca. Presentaron células tabulares la ornitófila perchera Grevillea robusta, las dos especies quiropterófilas y la autógama Stellaria media. Además, el mesofilo de las quiropterófilas fue más grueso. Finalmente, hubo diferencias en la turgencia celular (A. paucinervis, protógina) y en el grosor del mesofilo entre las flores masculinas y femeninas (Cytinus).  Conclusiones: Se cumplió el patrón esperado de existencia de células papilosas en corolas que contactan físicamente con los polinizadores, pero también aparecieron en corolas sin tal contacto. En especies con dicogamia y unisexualidad es aconsejable estudiar la microestructura corolina diferenciando entre los dos estados sexuales, ya que la turgencia celular o el grosor del mesofilo podrían diferenciarlos. También advertimos contra la amplia opinión de que ciertos tipos de polinizadores no interaccionan mecánicamente con la superficie epidérmica de la corola.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[mesophyll thickness]]></kwd>
<kwd lng="en"><![CDATA[nectar theft]]></kwd>
<kwd lng="en"><![CDATA[papillose cells]]></kwd>
<kwd lng="en"><![CDATA[sphingophily]]></kwd>
<kwd lng="en"><![CDATA[tabular cells]]></kwd>
<kwd lng="en"><![CDATA[zoophily]]></kwd>
<kwd lng="es"><![CDATA[Células papilosas]]></kwd>
<kwd lng="es"><![CDATA[células tabulares]]></kwd>
<kwd lng="es"><![CDATA[esfingofilia]]></kwd>
<kwd lng="es"><![CDATA[grosor del mesofilo]]></kwd>
<kwd lng="es"><![CDATA[robo de néctar]]></kwd>
<kwd lng="es"><![CDATA[zoofilia]]></kwd>
</kwd-group>
</article-meta>
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