<?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>0034-7744</journal-id>
<journal-title><![CDATA[Revista de Biología Tropical]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. biol. trop]]></abbrev-journal-title>
<issn>0034-7744</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Costa Rica]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-77442018000100394</article-id>
<article-id pub-id-type="doi">10.15517/rbt.v66i1.29013</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Los agroecosistemas cafetaleros modernos y su relación con la conservación de mariposas en paisajes fragmentados]]></article-title>
<article-title xml:lang="en"><![CDATA[Modern coffee agroecosystems and their relationship with butterflies conservation in fragmented landscapes]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pérez-García]]></surname>
<given-names><![CDATA[Oscar]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Benjamin]]></surname>
<given-names><![CDATA[Tamara J.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Tobar L.]]></surname>
<given-names><![CDATA[Diego Enrique]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto Politécnico Nacional  ]]></institution>
<addr-line><![CDATA[ Oaxaca]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Purdue University  ]]></institution>
<addr-line><![CDATA[ Indiana]]></addr-line>
<country>USA</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Centro Agronómico Tropical de Investigación y Enseñanza  ]]></institution>
<addr-line><![CDATA[Turrialba ]]></addr-line>
<country>Costa Rica</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2018</year>
</pub-date>
<volume>66</volume>
<numero>1</numero>
<fpage>394</fpage>
<lpage>402</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0034-77442018000100394&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0034-77442018000100394&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0034-77442018000100394&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El cambio de uso del suelo por la intensificación de la agricultura contribuye a la fragmentación de los bosques tropicales y la pérdida de la biodiversidad. En este sentido, a diferencia de los sistemas agroforestales (SAF) tradicionales, los SAF modernos son considerados de poca importancia para la conservación de la biodiversidad de los fragmentos de bosque. Sin embargo, existe una tendencia al establecimiento de SAF modernos. Debido a la sensibilidad a los cambios ambientales, se evaluó la diversidad de mariposas en SAF modernos de Coffea arabica y Erythrina poeppigiana (CP) y en combinación con Musa spp. (CPM) o Cordia alliodora (la única especie nativa de los SAF) (CPL), además de fragmentos de bosque muy húmedo premontano (FR) en el Corredor Biológico Volcánica Central-Talamanca, Costa Rica. En seis sitios representativos de cada sistema se establecieron tres transectos paralelos de 80 m cada uno y distanciados a 25 m entre los mismos. Cada cafetal y fragmento de bosque fue muestreado durante 1.5 horas en total para el registro de mariposas. Durante tres fechas de muestreo, se obtuvo un esfuerzo de muestreo de 4.5 horas/sitio y 27 horas en cada SAF y en FR. CP y CPM juntos tuvieron una composición de especies de mariposas diferente a la de CPL y FR. CP y CPM juntos resultaron con las especies de áreas abiertas Hermeuptychia hermes y Anartia jatrophae como indicadoras. CPL resultó con las especies de bosques secundarios Heliconus erato petiverana y Pareuptychia ocirrhoe como indicadoras. Por el contrario, FR resultó con diversas especies indicadoras típicas de bosques continuos tales como Pierella helvina incanescens, Caligo eurilochus y Morpho peleides limpida. Además, la riqueza de especies en FR fue mayor en relación a los SAF. Sin embargo, entre los SAF, CPL resultó con la mayor diversidad (Exp(H&#8217;)) de especies de áreas cerradas que CP. Así mismo, CPM tuvo una mayor abundancia de mariposas frugívoras que CP y CPL. En bosques fragmentados, los cafetales con sombras exóticas pueden ser mejores hábitats para mariposas de bosques si se combinan con árboles nativos y/o frutales.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Land use change by the intensification of agriculture contributes to tropical forest fragmentation and biodiversity loss. In this sense, in comparison with traditional agroforestry systems (AFS), modern AFS are considered irrelevant for the conservation of biodiversity of tropical forest fragments. However, there is an increasing trend toward the establishment of different types of modern AFS. Owing to the sensitivity to environmental changes, we evaluated the biodiversity of butterflies in AFS with Coffea arabica and Erythrina poeppigiana (CP), and intermixed with Musa spp. (CPM) or Cordia alliodora (the only native species of AFS) (CPL), as well as premontane very humid forest fragments in the Volcánica Central-Talamanca Biological Corridor, Costa Rica. In six representative sites of each system we set up three parallel 80 m line-transects, separated by a distance of 25 m. Each coffee farm and forest fragment (FR) was surveyed during 1.5 hours to record butterflies. All sites were sampled once a month from May to July 2007. We obtained 4.5 hours of sampling/site, and 27 hours of sampling/habitat. Both CP and CPM together had a butterflies&#8217; species composition which differed from CPL and FR. The indicator species of both CP and CPM together were Hermeuptychia hermes and Anartia jatrophae which are typical of open areas. CPL resulted with the species of secondary forests Heliconius erato petiverana and Pareuptychia ocirrhoe as indicators. In contrast, FR resulted with several indicator species typical of closed canopy forests such as Pierella helvina incanescens, Caligo eurilochus, and Morpho peleides limpida. Moreover, the richness of species was similar among coffee AFS. Furthermore, the richness of species of each coffee AFS was lower in comparison with FR. However, among coffee AFS, CPL harbored higher diversity (Exp(H&#8217;)) of forest butterflies than CP. Also, CPM was higher in abundance of frugivorous butterflies in relation with CP and CPL. In fragmented forests, coffee farms with exotic shade species combined at least with a native tree or fruit species, can be a better habitat for forest butterflies than those dominated by an exotic monospecific shade. Rev. Biol. Trop. 66(1): 394-402. Epub 2018 March 01.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[especies indicadoras]]></kwd>
<kwd lng="es"><![CDATA[gremios]]></kwd>
<kwd lng="es"><![CDATA[matriz de cafetales]]></kwd>
<kwd lng="es"><![CDATA[Papilionoidea]]></kwd>
<kwd lng="es"><![CDATA[preferencias de hábitat]]></kwd>
<kwd lng="es"><![CDATA[sistemas agroforestales]]></kwd>
<kwd lng="en"><![CDATA[agroforestry systems]]></kwd>
<kwd lng="en"><![CDATA[coffee matrix]]></kwd>
<kwd lng="en"><![CDATA[guilds]]></kwd>
<kwd lng="en"><![CDATA[habitat preferences]]></kwd>
<kwd lng="en"><![CDATA[indicator species]]></kwd>
<kwd lng="en"><![CDATA[Papilionoidea]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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