<?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>0065-1737</journal-id>
<journal-title><![CDATA[Acta zoológica mexicana]]></journal-title>
<abbrev-journal-title><![CDATA[Acta Zool. Mex]]></abbrev-journal-title>
<issn>0065-1737</issn>
<publisher>
<publisher-name><![CDATA[Instituto de Ecología A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0065-17372025000100139</article-id>
<article-id pub-id-type="doi">10.21829/azm.2025.4112784</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Estructura de la diversidad alfa, beta y aspectos ecológicos de los ensambles de flebotominos en tres poblaciones de la Península de Yucatán, México (Diptera: Psychodidae, Phlebotominae)]]></article-title>
<article-title xml:lang="en"><![CDATA[Structure of alpha, beta diversity and ecological aspects of phlebotomine assemblages in three populations of the Yucatan Peninsula, Mexico (Diptera: Psychodidae, Phlebotominae)]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rebollar-Téllez]]></surname>
<given-names><![CDATA[Eduardo A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ibáñez-Bernal]]></surname>
<given-names><![CDATA[Sergio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández-Cabrera]]></surname>
<given-names><![CDATA[Francisco]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Autónoma de Nuevo León Facultad de Ciencias Biológicas Laboratorio de Entomología Médica]]></institution>
<addr-line><![CDATA[ Nuevo León]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Red de Ambiente y Sustentabilidad, Instituto de Ecología A. C.  ]]></institution>
<addr-line><![CDATA[ Veracruz]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad Autónoma de Nuevo León Facultad de Ciencias Físico Matemáticas ]]></institution>
<addr-line><![CDATA[ Nuevo León]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2025</year>
</pub-date>
<volume>41</volume>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0065-17372025000100139&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0065-17372025000100139&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0065-17372025000100139&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen La leishmaniasis cutánea es endémica en la Península de Yucatán y es causada principalmente por el parásito Leishmania mexicana. En 1965 se reportó la competencia vectorial del flebotomino Bichromomyia olmeca. No obstante, estudios de distribución geográfica de la especie y de la zona reconocida de transmisión de leishmaniasis mostraron que no existía una correspondencia total, por lo tanto, se hipotetizó que otras especies de flebotominos participaban en la transmisión. Las especies sospechosas son Lutzomyia cruciata, Psathyromyia shannoni y Psychodopygus panamensis. Un aspecto fundamental para entender cómo participan estas especies en la transmisión de Le. mexicana es analizar y describir los patrones de diversidad alfa y beta de los ensambles de flebotominos. El objetivo del presente trabajo fue analizar cuantitativamente atributos biológicos relacionados con la diversidad alfa y beta, así como registrar los patrones de actividad de picadura de las especies de importancia médica. En las localidades de Becanchén (BE), municipio Tekax, Yucatán, La Libertad (LA), municipio Escárcega, Campeche y Santa Isabel (SI), municipio Carrillo Puerto, Quintana Roo, se llevaron a cabo muestreos entre 2001-2002, usando trampas de luz CDC, trampas Disney y trampas Shannon. En total se capturaron 4,511 especímenes siendo 1,098 para (BE) 1,394 para (LA) y 2,019 para (SI), y con el índice estandarizado SISA se encontró que las especies con mayor representación fueron: Dampfomyia deleoni, Lu. cruciata, Brumptomyia mesai y Bi. olmeca. Pese a variaciones entre localidades, los métodos de captura de trampas CDC y Shannon fueron significativamente diferentes a las trampas Disney. La riqueza específica fue de 7, 12 y 9 especies para Becanchén, La Libertad y Santa Isabel, respectivamente. Se encontró mayor dominancia de Simpson en BE (0.39), seguido de SI (0.26) y LA (0.21); en cuanto al índice alfa de Fisher, los valores fueron 1.80 (LA), 1.21 (SI) y 0.99 (BE) y para la heterogeneidad de Shannon, los valores fueron: 1.13 (BE), 1.74 (LA) y 1.58 (SI). Las curvas de rango abundancia indicaron que la jerarquía por dominancia de las especies en BE fue Br. mesai seguida de Lu. cruciata, para LA fue Da. deleoni y Br. olmeca, mientras que para SI fue Da. deleoni y Br. mesai. La diversidad beta mediante el modelo de Morisita-Horn, indicó que LA y SI, eran más similares en el ensamble de especies comparado con BE. Un análisis de escalamiento no-métrico multidimensional confirmó que la ordenación de la variación era traslapada para LA y SI, y distinta con BE. La tasa de picadura de flebotominos hembra se calculó para Lu. cruciata en BE, para Lu. cruciata y Bi. olmeca en LA y para Lu. cruciata y Pa. shannoni en SI. Existieron correlaciones significativas de Lu. cruciata con la humedad y temperatura en LA y SI. Finalmente se discute el significado de los ensambles en el contexto de la transmisión de leishmaniasis.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract The Cutaneous leishmaniasis is endemic in the Yucatan Peninsula and is caused mainly by the parasite Leishmania mexicana. In 1965, the vectorial competence of the sand fly Bichromomyia olmeca was reported as a vector. However, studies of the geographic distribution of the species and the recognized human leishmaniasis area of transmission showed that there was no total correspondence, therefore, it was hypothesized that other sand fly species participated in the transmission. These suspected species are Lutzomyia cruciata, Psathyromyia shannoni and Psychodopygus panamensis. A fundamental aspect to understand how these species participate in the transmission of Le. mexicana is to analyze and describe the alpha and beta diversity patterns of the sand fly assemblages. The objective of the present work was to quantitatively analyze biological attributes related to alpha and beta diversity, as well as to record the bite activity patterns of the species of medical importance. In the localities of Becanchén (BE), municipality Tekax, Yucatán, La Libertad (LA), municipality Escárcega, Campeche and Santa Isabel (SI), municipality Carrillo Puerto, Quintana Roo, sampling was carried out between 2001-2002, using CDC light traps, Disney traps, and Shannon traps. A total of 4,511 specimens were captured, 1,098 for (BE), 1,394 for (LA), and 2,019 for (SI). Using the standardized SISA index, it was found that the species with the highest representation were: Dampfpmyia deleoni, Lu. cruciata, Brumptomyia mesai, and Bi. olmeca. Despite variations between localities, the capture methods of CDC and Shannon traps were significantly different from those of Disney traps. The species richness was 7, 12, and 9 for Becanchén, La Libertad, and Santa Isabel, respectively. Simpson's dominance was found highest in BE (0.39), followed by SI (0.26) and LA (0.21). Fisher's alpha index values were 1.80 (LA), 1.21 (SI) and 0.99 (BE). Shannon's heterogeneity values were: 1.13 (BE), 1.74 (LA) and 1.58 (SI). Abundance rank curves indicated that the species dominance hierarchy in BE was Br. mesai followed by Lu. cruciata, for LA it was Da. deleoni and Br. olmeca, while for SI it was Da. deleoni and Br. mesai. Beta diversity using the Morisita-Horn model indicated that LA and SI were more similar in species assemblage compared to BE. A multidimensional non-metric scaling analysis confirmed that the ordering of variation was overlapped for LA and SI, and different with BE. The biting rate of female sandflies was calculated for Lu. cruciata in BE, for Lu. cruciata and Bi. olmeca in LA and for Lu. cruciata and Pa. shannoni in SI. There were significant correlations of Lu. cruciata with humidity and temperature in certain locations such as LA and SI. Finally, the significance of the assemblages in the context of leishmaniasis transmission is discussed.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[leishmaniasis]]></kwd>
<kwd lng="es"><![CDATA[diversidad]]></kwd>
<kwd lng="es"><![CDATA[incriminación de vectores]]></kwd>
<kwd lng="en"><![CDATA[leishmaniasis]]></kwd>
<kwd lng="en"><![CDATA[diversity]]></kwd>
<kwd lng="en"><![CDATA[vector incrimination]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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