34 results on '"Carrillo-Ruiz, Hortensia"'
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2. Anatomical Description of the Reproductive System and Maturation States in Females of Omorgus suberosus (Fabricius) (Coleoptera: Trogidae)
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Sánchez-Carrillo, Marcela, Huerta, Carmen, Carrillo-Ruiz, Hortensia, and Escobar, Federico
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- 2017
3. Aspectos comparativos del sistema reproductivo interno de los machos en especies de Melolonthinae, Dynastinae y Rutelinae (Coleoptera: Scarabaeoidea) de México
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Martínez M., Imelda, Rivera-Gasperín, Sara L., Carrillo-Ruiz, Hortensia, and Morón, Miguel A.
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- 2021
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4. Estructura y composición de la comunidad de escarabajos (Coleoptera: Scarabaeoidea) en el cerro Chacateca, Zapotitlán, Puebla, México
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Trujillo-Miranda, Alma L., Carrillo-Ruiz, Hortensia, Rivas-Arancibia, Sombra P., and Andrés-Hernández, A. Rosa
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- 2016
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5. Description of immature stages of Hoplia mexicana Harold and H. squamifera Burmeister (Coleoptera, Melolonthidae, Hopliinae)
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Morón, Miguel Ángel, Ramírez-Ponce, Andrés, Ramírez-Salinas, Concepción, and Carrillo-Ruiz, Hortensia
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- 2016
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6. Variaciones de la comunidad de visitadores florales de Bursera copallifera (Burseraceae) a lo largo de un gradiente de perturbación antropogénica
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Patricia Rivas-Arancibia, Sombra, Bello-Cervantes, Eribel, Carrillo-Ruiz, Hortensia, Rosa Andrés-Hernández, Agustina, María Figueroa-Castro, Dulce, and Guzmán-Jiménez, Silvia
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- 2015
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7. FAUNA DE SCARABAEOIDEA (INSECTA: COLEOPTERA) DE CALMECA, TEPEXCO, PUEBLA, MEXICO
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Carrillo-Ruiz, Hortensia, Guerra-González, Irma, Sánchez-Carrillo, Marcela, Morón, Miguel A., and Rivas-Arancibia, Sombra P.
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- 2017
8. Positive Edge Effects of Natural Habitats Produce Matching Response in Beetle Population and Plant Morphometry in Amaranth Crop
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Álvarez, Hugo A., primary, Clemente-Orta, Gemma, additional, Carrillo-Ruiz, Hortensia, additional, López-Olguín, Jesús F., additional, Jiménez-García, Daniel, additional, and Morón, Miguel A., additional
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- 2022
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9. Patrones de distribución del género Zanthoxylum L. (Rutaceae) en México
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Puga-Jiménez, Ana Laura, Andrés-Hernández, Agustina Rosa, Carrillo-Ruiz, Hortensia, Espinosa, David, and Rivas-Arancibia, Sombra Patricia
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- 2013
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10. Diversidad de coleópteros copro-necrofagos en el 'Rancho Canaletas', Paso del Macho Veracruz, México
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Yanes-Gómez, Gonzalo, Pérez-Méndez, Marisol, Ramírez-González, Oscar Iván, Ángel Morón, Miguel, Carrillo-Ruiz, Hortensia, and Romero-López, Ángel Alonso
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- 2015
11. Plant morphometry matches beetle diversity: effects of natural adjacent vegetation on grain Amaranth crop under small-holder conditions
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Álvarez, Hugo Alejandro, primary, Clemente-Orta, Gemma, additional, Carrillo-Ruiz, Hortensia, additional, López-Olguín, Jesus, additional, Jiménez-García, Daniel, additional, and Morón, Miguel Ángel, additional
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- 2021
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12. Comparative aspects of the internal reproductive system of males in species of Melolonthinae, Dynastinae, and Rutelinae (Coleoptera: Scarabaeoidea) from Mexico
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Martínez M., Imelda, primary, Rivera-Gasperín, Sara L., additional, Carrillo-Ruiz, Hortensia, additional, and Morón, Miguel A., additional
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- 2021
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13. Fauna de coleoptera melolonthidae (Scarabaeoidea) en el Rancho Canaletas, Paso del Macho, Veracruz, Mexico
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Rivera-Gasperín, Sara Lariza, Carrillo-Ruiz, Hortensia, Morón, Miguel Ángel, and Yanes-Gómez, Gonzalo
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- 2013
14. Beetles in Amaranthus hypochondriacus L. during the Dry Season
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Álvarez, Hugo A., primary, Carrillo-Ruiz, Hortensia, additional, López-Olguín, Jesús F., additional, Jiménez-García, Daniel, additional, and Morón†, Miguel A., additional
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- 2019
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15. Edge Effects of an Ecological Gradient on Beetle Functionality: A Case Study in Amaranthus hypochondriacus.
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Álvarez, Hugo Alejandro, Clemente-Orta, Gemma, Carrillo-Ruiz, Hortensia, López-Olguín, Jesús F., Jiménez-García, Daniel, and Morón, Miguel A.
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DECIDUOUS forests , *SPECIES diversity , *CHRYSOMELIDAE , *FUNCTIONAL analysis , *NATURE reserves - Abstract
Ecological gradients are important for species in nature. However, there is a need to better understand how varying levels of disturbance influence the functional roles of beetle species within a crop area characterized by different types of natural vegetation. Here, we test such effects by studying a perturbation gradient – an ecological gradient that transitions from a natural area near the ecotone of a deciduous forest (a transitional zone between crops and forest) to a crop. The beetle specimens were collected along transects parallel to the ecotone, and their functional diversity was assessed using a clustering analysis and functional indices. We identified 21 species of beetles, and the highest species richness was observed in the Chrysomelidae family. A functional analysis revealed two main groups, including primary consumers (phytophages) and entomophagous beetles. The hedge area exhibited functional richness similar to the natural area. However, the functional evenness was consistently low across all the areas. The presence of natural habitats positively influenced beetle functionality and potentially impacted the abundance of deleterious species of beetles and their establishment at a low spatial scale. These findings underscore the importance of considering different spatial-scale-dynamics in agroecosystems and highlight the potential role of natural habitats in fostering functionality to indirectly control pests. [ABSTRACT FROM AUTHOR]
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- 2024
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16. Floral morphometry, anthesis, and pollination success of Mammillaria pectinifera (Cactaceae), a rare and threatened endemic species of Central Mexico
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Valverde, Pedro Luis, Jiménez-Sierra, Cecilia, López-Ortega, Gerardo, Zavala-Hurtado, José Alejandro, Rivas-Arancibia, Sombra, Rendón-Aguilar, Beatriz, Pérez-Hernández, Marco Aurelio, Cornejo-Romero, Amelia, and Carrillo-Ruiz, Hortensia
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- 2015
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17. Un primer paso hacia el reconocimiento automático de escarabajos
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Jiménez, Caleb, primary, Carrillo, Maya, additional, Carrillo-Ruiz, Hortensia, additional, Sandoval S., María de Lourdes, additional, and Alfredo Moctezuma, Luis, additional
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- 2017
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18. New Records of Stagmomantis limbata for Three States of Central Mexico
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Álvarez, Hugo A., primary, Carrillo-Ruiz, Hortensia, additional, Jiménez-García, Daniel, additional, and Morón, Miguel A., additional
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- 2017
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19. Anatomical Description of the Reproductive System and Maturation States in Females ofOmorgus suberosus(Fabricius) (Coleoptera: Trogidae)
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Sánchez-Carrillo, Marcela, primary, Huerta, Carmen, additional, Carrillo-Ruiz, Hortensia, additional, and Escobar, Federico, additional
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- 2017
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20. Abundance of Insect Fauna Associated withAmaranthus hypochondriacusL. Crop, in Relation to Natural Living Fences
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Álvarez, Hugo A., primary, Carrillo-Ruiz, Hortensia, additional, Jiménez-García, Daniel, additional, and Morón, Miguel A., additional
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- 2017
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21. Hoplia mexicana Harold 1869
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Morón, Miguel Ángel, Ramírez-Ponce, Andrés, Ramírez-Salinas, Concepción, and Carrillo-Ruiz, Hortensia
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Coleoptera ,Hoplia ,Insecta ,Arthropoda ,Hoplia mexicana ,Melolonthidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Hoplia mexicana Harold, 1869 Third instar (Figs. 1–11 and 13). Description. Head (Fig. 2). Maximum width of head capsule: 1.8–2.0 mm. Surface of cranium smooth, with scattered minute punctures, pale yellowish. Frontal and epicranial sutures hidden. Frons with 2 exterior frontal setae, 3–4 posterior frontal setae, 1 anterior frontal seta, 1 anterior angle seta, 3 dorsoepicranial setae, 8–9 epicranial setae on each side and 7–9 setae behind each antennal support. Clypeus with 2 central setae and 4 lateral seta on each side. Labrum nearly symmetrical with rounded lateral margins irregularly bordered, anterior margin projected forward with irregular border, 6–7 posterior setae, 1 central seta and 3–4 lateral setae on each side. Stemmata absent. Epipharynx (Fig. 5) 1.0– 1.1 mm wide, 0.8–0.9 mm long, epizygum absent and zygum as a irregular, ovate, reddish yellow plate. Haptomerum weakly raised, with 4 heli; each plegmatia formed by 8–10 short plegmata; proplegmatia absent. Each acanthoparia with 10–12 spinose setae. Dexiophoba and laeophoba absent. Dexiotorma narrowed, slightly sinuose. Laeotorma elongate and narrowed, with sclerotized plate unciform, raised. Sense cone short. Crepis weakly defined. Left chaetoparia with 28–30 spinose and medium size setae mixed. Right chaetoparia with 30–36 short, stout setae. Mandibles (Figs. 3 and 4) without ventral stridulatory area; scissorial area in both mandibles without distal blade. Right mandible with 1 small preapical tooth, inner margin simply curved, and distal lobe (M1) of molar area scarcely developed. Calx short. Left mandible with 1 small preapical tooth, inner margin simply curved, brustia moderately setose.Acia absent. Maxillae (Figs. 6–9). Mala with 1 uncus on apex of galea, 3 unci surrounded by 3–4 stout heli on apex of lacinia; stridulatory area with 8 small teeth with anteriorly directed points. Hypopharyngeal sclerome (Fig. 10) asymmetrical with raised and curved projection on the right side. Fourth antennomere elongate, with distal half narrowed, with 1 ovate, dorsal sensory spot on basal half and 2 ventral sensory spots. Thorax. Respiratory plates light yellow, scarcely curved, “C” shaped (Figs. 1 and 13) 0.12–0.14 mm long, 0.10–0.11 mm wide, bulla small, slightly raised, rounded, distance between lobes longer than dorso-ventral diameter of bulla; microscopic holes of respiratory plate elongate-oval in outline and arranged in irregular transverse rows. Lateral sclerome of pronotum not defined. Proprescutum with 20–22 long setae regularly distributed; proscutum with 8–9 slender long setae; mesoprescutum with transverse row of 10–12 long setae; mesoscutum with 12–16 setae; mesoscutellum with row of 8–10 slender long setae; metaprescutum with transverse row of 12–16 mixed short and long setae; metascutum with 10–12 setae; metascutellum with transverse row of 10–12 mixed short and long setae (Figs. 1 and 13). Protarsal claws long, narrowed, sharply pointed, with 1 prebasal inner seta and 1 lateral external seta, moderately longer than mesotarsal claws; mesotarsal claws long, sharply pointed, with pre-basal and lateral setae; metatarsal claw short, rounded, with 2 setae, much shorter than mesotarsal claws. Apical metatarsomere shortened, rounded, with ventral side clearly convex. Abdomen. Respiratory plates light yellow, slightly curved, “C” shaped; on segments I–IV with similar diameter, 0.12–0.13 mm long, 0.10 mm wide; plates on segments V–VII are slightly smaller, 0.10–0.11 mm length, 0.09 mm width. Plate on segment VIII is smaller than preceding. Dorsa of abdominal segments I–VI each with dense vestiture of yellow stout, short setae; dorsa of segments VII–IX with transverse rows of 20–28 slender, short setae. Venter of abdominal segments I–VIII with transverse rows of 14–18 slender, long setae; venter of segment IX with transverse rows of 12–16 mixed short and long setae. Raster (Fig. 11) with each palidia formed by 9–11 pali, convergent toward basal and distal extremes, septula wide, oval; tegilla with 20–26 short, stout setae; campus with 14–18 slender, short setae; barbula much more densely setose.Dorsal anal lip with dense vestiture of short setae. Ventral anal lip with scattered short setae toward sides and distal border narrowly notched at middle. Anal slit “Y” shaped. Approximate dorsal body length 16–17 mm. Description: body length 7.5–7.8 mm. Widest width 4.4–4.5 mm. Head. Surface glabrous, strongly deflexed; frons convex with two rounded prominences; clypeus widely concave on the center; labrum, mandibles, maxillae and palps discernible; antennal theca briefly expanded, stout with apex rounded; eyes small (Fig. 14). Thorax: surface glabrous. Pronotum convex, surface slightly irregular, anterior angles prominent, posterior angles rounded. Meso- and metanotum well-differentiated. Elytral and posterior wing thecae closely appressed, curved ventrally around the body; elytral thecae with irregular depressions and large, prominent, humeral tubercles (Figs. 12 and 15); thecae of the wings slightly longer than elytral thecae. Protibiae with apical and preapical tubercles clearly developed. Meso and metatibiae with apical tubercle. Abdomen: segments I–VI clearly wider and shorter than the distal segments VII–VIII, without dioneiform organs, but segments II–IV with pairs of prominent tubercles and segment V with increased posterior border (Figs. 12 and 15–16). Pleural lobes rounded. Spiracle I elongate, with fine peritreme and covered by wing thecae; spiracles II–IV ovate and high, prominent, with narrow sclerotized peritreme; spiracles V–VIII closed. Sutures between segments VIII and X not complete, partially fused. Last segment slightly pruinose, without urogomphi. Last abdominal segment of male with large dorsal and lateral rounded prominences, and genital ampulla ventrally exposed (Figs. 12 and 14–16); female without such prominences at the apex of abdomen. Specimens examined. Four third instar larvae, four pupae and two exuviae of third instar larvae reared to adults, collected at Mexico: Oaxaca: Santa María Tlahuitoltepec municipality, Cerro Zempoaltepetl, 2400 m, 8-VI-2010, A. Ramírez col. (IEXA). Comments. The third instar larvae of H.mexicana resemble those of H. callipyge and H. equina, but H. mexicana has 4 heli on haptomerum, and palidia with well-defined septula. Hoplia callipyge and H. equina each have1 helus on the haptomerum and only subtriangular teges of long hamate setae with curved tips. The dense setiferous vestiture on the dorsum of abdominal segments I–VI and the sides of the last segment, aid in distinguishing H. mexicana from the known larvae of other Mexican melolonthine scarabs. Projections on the humeral area of the elytra and the middle of the abdominal segments of the pupae of both sexes may act as auxiliary supports during pupal development. These projections possibly aid in regulating humidity near the body wall. This type of structure is also observed in pupae of some Scarabaeinae (Edmonds and Halffter, 1978), and Ceratocanthinae (Morón and Arce, 2003). Biology. Hoplia mexicana is known only from the northern mountains of the Mexican state of Oaxaca, at localities with elevations between 2300 and 2500 m. Larvae have been collected in rich organic soil of oak and coniferous forest. Adults are rarely attracted to electric lights during summer, and their host plants are unknown., Published as part of Morón, Miguel Ángel, Ramírez-Ponce, Andrés, Ramírez-Salinas, Concepción & Carrillo-Ruiz, Hortensia, 2016, Description of immature stages of Hoplia mexicana Harold and H. squamifera Burmeister (Coleoptera, Melolonthidae, Hopliinae), pp. 1-7 in Revista Brasileira de Entomologia 60 (1) on pages 2-4, DOI: 10.1016/j.rbe.2015.11.012, http://zenodo.org/record/8111182, {"references":["Harold, E., 1869. Scarabaeidae. In: Gemminger, M., Harold, E. (Eds.), Catalogus Coleopterorum Hucusque Descriptorum Synonymicus et Systematicus, vol. 4. E. H. Gummi, Munich, pp. 979 - 1346.","Edmonds, W. D., Halffter, G., 1978. Taxonomic review of immature dung beetles of the subfamily Scarabaeinae (Coleoptera: Scarabaeidae). Syst. Entomol. 3, 307 - 331.","Moron, M. A., Arce, R., 2003. Description of third instar larva and pupa of Ceratocanthus relucens (Bates) (Coleoptera: Scarabaeidae; Ceratocanthinae). Coleopterists Bull. 57, 245 - 253."]}
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- 2015
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22. Hoplia squamifera Burmeister 1844
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Morón, Miguel Ángel, Ramírez-Ponce, Andrés, Ramírez-Salinas, Concepción, and Carrillo-Ruiz, Hortensia
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Coleoptera ,Hoplia ,Insecta ,Arthropoda ,Melolonthidae ,Animalia ,Hoplia squamifera ,Biodiversity ,Taxonomy - Abstract
Hoplia squamifera Burmeister, 1844 Third instar (Figs. 17–24). Description. Head (Fig. 18). Maximum width of head capsule: 2.1–2.4 mm. Surface of cranium smooth, with scattered minute punctures, pale yellowish. Frontal and epicranial sutures hidden. Frons with 2 exterior frontal setae, 1 posterior frontal seta, anterior frontal seta absent, 1 anterior angle seta, 3–4 dorsoepicranial, 14–18 epicranial setae on each side and 6–8 setae behind each antennal support. Clypeus with 2 central setae and 4 lateral setae on each side. Labrum nearly symmetrical with rounded lateral margins irregularly bordered, anterior margin projected forward with irregular border, basal transverse keel with 5 posterior setae, 1 anterior-central seta and 5–6 lateral setae on each side. Stemmata absent. Epipharynx (Fig. 21) 1.6–1.9 mm wide, 1.0– 0.2 mm long. Epizygum absent and zygum as irregular, ovate, reddish yellow plate. Haptomerum weakly raised, with 4 heli; each plegmatia formed by 9–10 short plegmata; proplegmatia absent. Each acanthoparia with 9–10 spinose setae. Dexiophoba and laeophoba absent. Dexiotorma narrowed, slightly curved. Laeotorma elongate and narrowed with sclerotized plate unciform, raised. Sense cone short. Crepis weakly defined. Left chaetoparia with 30–34 spinose and medium size setae mixed. Right chaetoparia with 28–30 short, stout setae. Mandibles (Figs. 19 and 20) without ventral stridulatory area; scissorial area in both mandibles without distal blade. Right mandible with 1 small rounded, preapical tooth, inner margin simply curved, and distal lobe (M1) of molar area scarcely developed. Calx short. Left mandible without preapical tooth, inner margin simply curved, brustia moderately setose. Acia absent. Maxillae (Fig. 23). Mala with 1 uncus on apex of galea, 3 unci surrounded by 3–4 stout heli on apex of lacinia; stridulatory area with 10–11 small teeth with anteriorly directed points. Hypopharyngeal sclerome (Fig. 22) asymmetrical with curved projection on the right side. Fourth antennomere elongate, with distal half narrowed, with 1 ovate, dorsal sensory spot on basal half and 2 ventral sensory spots. Thorax. Respiratory plates light yellow, scarcely curved, “C” shaped (Fig. 17) 0.11–0.15 mm long, 0.10–0.12 mm wide, bulla small, slightly raised, rounded, distance between lobes longer than dorso-ventral diameter of bulla; microscopic holes of respiratory plate elongate-oval in outline and arranged in irregular transverse rows. Lateral sclerome of pronotum not defined. Proprescutum with 14–18 long setae regularly distributed; proscutum with 5–6 slender long setae; mesoprescutum with transverse row of 8–9 long setae; mesoscutum with 10–12 setae; mesoscutellum with row of 6–8 slender long setae; metaprescutum with transverse row of 9–12 mixed short and long setae; metascutum with 8–10 setae; metascutellum with transverse row of 6–8 mixed short and long setae (Fig. 17). Protarsal claws long, narrowed, sharply pointed, with 1 pre-basal inner seta and 1 lateral external seta, moderately longer than mesotarsal claws; mesotarsal claws long, sharply pointed, with pre-basal and lateral setae; metatarsal claw short, rounded, with 2 setae, much shorter than mesotarsal claws. Apical metatarsomere shortened, rounded, with ventral side clearly convex. Abdomen. Respiratory plates light yellow, slightly curved, “C” shaped; on segments I–IV with similar diameter, 0.13–0.14 mm long, 0.11 mm wide; plates on segments V–VII slightly smaller, 0.11–0.12 mm long, 0.10 mm wide. Respiratory plate on segment VIII smaller than plate on preceding segment. Dorsa of abdominal segments I–VI each with dense vestiture of yellow stout, short setae; dorsa of segments VII–IX with transverse rows of 18–20 slender, short setae. Venter of abdominal segments I–VIII with transverse rows of 10–12 slender, long setae; venter of segment IX with transverse rows of 10–12 mixed short and long setae. Raster (Fig. 24) with each palidia formed by 10–12 pali, convergent toward basal and distal extremes, septula wide, oval; tegilla with 24–30 short, stout setae; campus with 14–16 slender, short setae; barbula densely setose. Dorsal anal lip with dense vestiture of short setae. Ventral anal lip with scattered short setae at sides and distal border narrowly notched at middle. Anal slit “Y” shaped. Approximate dorsal body length 16–18 mm. Pupa (Figs. 25 and 26). Description: body length 7.8–8.1 mm. Widest width 4.5–4.6 mm. Head. Surface glabrous, strongly deflexed; frons convex with two rounded prominences; clypeus widely concave on the center; labrum, mandibles, maxillae and palps discernible; antennal theca briefly expanded, stout with apex rounded; eyes small (Fig. 25). Thorax: surface glabrous. Pronotum convex, surface slightly irregular, anterior angles briefly prominent, posterior angles widely rounded. Meso- and metanotum well-differentiated. Elytral and posterior wing thecae closely appressed, curved ventrally around body; elytral thecae with irregular longitudinal striae and large, prominent, semiconical humeral tubercles (Figs. 25 and 26); thecae of the wings slightly longer than elytral thecae. Protibiae with apical and preapical tubercles clearly developed. Meso and metatibiae with apical tubercle. Abdomen: segments I–VI clearly wider and shorter than the distal segments VII–VIII, without dioneiform organs, but segments II–IV with pairs of prominent tubercles and segment V with thicker posterior border (Figs. 25 and 26). Pleural lobes rounded. Spiracle I elongate, with fine peritreme partially covered by wing thecae; spiracles II–IV ovate and high, prominent, with narrow sclerotized peritreme; spiracles V–VIII closed. Sutures between segments VIII and X incomplete, partially fused. Last segment slightly pruinose, without urogomphi. Last abdominal segment of male with dorsal and lateral rounded prominences, and genital ampulla ventrally exposed (Fig. 26); female without such abdominal prominences (Fig. 25). Specimens examined. Seven third instar larvae, collected at Mexico: Chiapas, Amatenango del Valle municipality, El Madronal, 2400 m, 20-I-1997, corn field, C. Ramírez col. (IEXA). Two pupae and 2 exuviae of third instar larvae reared to adults, with same data, except 24-X-2005 (IEXA). Two third instar larvae: Chiapas, Amatenango del Valle, 28-X-1996, corn field, C. Ramírez; 4 third instar larvae with same data, except 4-XI-1996; 5 third instar larvae 24-IX-2001 (IEXA, ECOSUR). Comments. The larvae of Hoplia squamifera resemble those of H. mexicana, but lack antero-frontal setae, have 9–10 wide plegmata on each plegmatia, and have wide septula, whereas Hoplia mexicana have 2 antero-frontal setae, 7–8 narrow plegmata on each plegmatia and narrower septula. Pupae of both Hoplia mexicana, and H. squamifera lack urogomphi and dioneiform organs. This fact is very interesting because, as far as we know, no other scarab group possesses such a combination of characters. For instance, with the exception of Manopus biguttatus Laporte, 1840 (Neita-Moreno et al., 2012), known pupae of Melolonthinae have urogomphi and lack dioneiform organs (Table 1). On the other hand, known pupae of Rutelinae and Dynastinae, lack urogomphi but, in contrast, have dioneiform organs (Morón, 1993). With the combination of these characters, and the unique paired supporting organs in the humeri and tergites, the pupae of Hopliinae are very distinct from other subfamilies of Melolonthidae. Description of the pupae of many other genera of Melolonthidae surely will offer more characters to be tested in future phylogenetic analyses of Scarabaeoidea. Biology. Hoplia squamifera has been recorded from the Mexican mountains of northern Chiapas and Oaxaca states, southern Veracruz state, and in western Guatemala at localities with elevations between 1200 and 2100 m. Larvae have been collected in soil of corn fields in northern Chiapas, Mexico. Adults are frequently attracted to electric lights during spring and summer, but their host plants are unknown., Published as part of Morón, Miguel Ángel, Ramírez-Ponce, Andrés, Ramírez-Salinas, Concepción & Carrillo-Ruiz, Hortensia, 2016, Description of immature stages of Hoplia mexicana Harold and H. squamifera Burmeister (Coleoptera, Melolonthidae, Hopliinae), pp. 1-7 in Revista Brasileira de Entomologia 60 (1) on pages 4-6, DOI: 10.1016/j.rbe.2015.11.012, http://zenodo.org/record/8111182, {"references":["Burmeister, H. C. C., 1844. Handbuch der Entomologie (Coleoptera Lamellicornia Anthobia et Phyllophaga Systellochela) vol. 4, part 1. T. C. F. Enslin, Berlin.","Moron, M. A., 1986. El genero Phyllophaga en Mexico. Morfologia, Distribucion y Sistematica Supraespecifica (Insecta: Coleoptera). Instituto de Ecologia, Mexico, Publ. 20.","Moron, M. A., Nogueira, G., 2015. Descripcion de los estados inmaduros de Polyphylla conspersa Burmeister (Coleoptera: Melolonthidae: Melolonthinae) con observaciones sobre su biologia. Boletin Sociedad Entomologica Aragonesa 57.","Neita-Moreno, J. C., Moron, M. A., Zuluaga-Correa, C. A., 2012. Description of the immature stages of four species of Macrodactylini (Coleoptera: Melolonthidae: Melolonthinae). Neotrop. Entomol. 41, 150 - 162.","Moron, M. A., Salvadori, J. R., 2006. Third stage larva and pupa of Demodema brevitarsis Blanchard (Coleoptera: Scarabaeidae: Melolonthinae). Proc. Entomol. Soc. Washington 108, 511 - 518.","Ramirez-Salinas, C., Moron, M. A., Castro-Ramirez, A., 2011. Descripcion de los inmaduros de cuatro especies de Phyllophaga, Paranomala y Macrodactylus (Coleoptera: Melolonthidae) de los Altos de Chiapas, Mexico. Acta Zoologica Mexicana (n. s.) 27, 527 - 545.","Mico, E., Moron, M. A., Galante, E., 2003. New larval descriptions and biology of some New World Anomalini beetles (Coleoptera: Scarabaeoidea: Rutelinae). Ann. Entomol. Soc. Am. 96, 597 - 614.","Moron, M. A., Paucar-Cabrera, A., 2003. Larvae and pupae of species of Macraspis Macleay (Coleoptera: Scarabaeidae: Rutelinae: Rutelini). Can. Entomol. 135, 467 - 491.","Jameson, M. L., Moron, M. A., 2001. Descriptions of the larvae of Chlorota cincticollis Blanchard and Chasmodia collaris (Blanchard) (Scarabaeidae: Rutelinae: Rutelini) with a key to the larvae of the American genera of Rutelini. Coleopterists Bull. 55, 385 - 396.","Pardo-Locarno, L. C., Moron, M. A., 2007. Larva and pupa of Chrysophora chrysochlora (Coleoptera: Scarabaeidae: Rutelinae: Rutelini). Can. Entomol. 139, 80 - 86.","Pardo-Locarno, L. C., Moron, M. A., Montoya-Lerma, J., 2006 b. Descripcion de los estados inmaduros de Leucothyreus femoratus (Coleoptera: Melolonthidae, Rutelinae: Geniatini) con notas sobre su biologia e importancia agricola en Colombia. Folia Entomologica Mexicana 45, 179 - 193.","Ramirez-Salinas, C., Moron, M. A., Castro-Ramirez, A., 2004. Descripcion de los estados inmaduros de tres especies de Anomala, Ancognatha y Ligyrus (Coleoptera: Melolonthidae: Rutelinae y Dynastinae) con observaciones de su biologia. Acta Zoologica Mexicana (n. s.) 20, 67 - 82.","Pardo-Locarno, L. C., Moron, M. A., Gaigl, A., 2006 a. Los estados inmaduros de Coelosis biloba (Linne, 1767) (Coleoptera: Melolonthidae: Dynastinae) y notas sobre su biologia. Revista Mexicana de Biodiversidad 77, 215 - 224.","Moron, M. A., 1995 b. Review of the Mexican species of Golofa Hope (Coleoptera: Melolonthidae, Dynastinae). Coleopterist's Bull. 49, 343 - 386.","Moron, M. A., 1987. Los estados inmaduros de Dynastes hyllus Chevrolat (Col. Melolonthidae, Dynastinae) con observaciones sobre su biologia y el crecimiento alometrico del imago. Folia Entomologica Mexicana 72, 33 - 74.","Neita-Moreno, J. C., Oliveira, M. C., Moron, M. A., 2014. Larval and pupal descriptions of two Aegopsis species (Coleoptera: Melolonthidae: Dynastinae). Florida Entomol. 97, 114 - 125.","Ramirez-Salinas, C., Castro-Ramirez, A., Moron, M. A., 2001. Descripcion de la larva y la pupa de Euphoria basalis (G & P.) (Coleoptera: Melolonthidae; Cetoniinae). Acta Zoologica Mexicana (n. s.) 83, 73 - 82.","Moron, M. A., Arce, R., 2002. Descriptions of the immature stages of five Mexican species of Gymnetini (Coleoptera: Scarabaeidae: Cetoniinae). Proc. Entomol. Soc. Washington 104, 1036 - 1054.","Nogueira, G., Moron, M. A., Fierros-Lopez, H. E., Navarrete-Heredia, J. L., 2004. The immature stages of Neoscelis dohrni (Westwood) (Coleoptera: Scarabaeidae: Cetoniinae: Goliathini) with notes on the adult behavior. Coleopterists Bull. 58, 171 - 183.","Moron, M. A., 1983. Los estados inmaduros de Inca clathrata sommeri Westw (Col. Melolonthidae, Trichiinae). Folia Entomologica Mexicana 56, 31 - 51.","Moron, M. A., 1995 a. Larva and pupa of Archedinus relictus Moron & Krikken (Coleoptera: Melolonthidae, Trichiinae, Incaini). Pan-Pacific Entomol. 71, 237 - 244.","Moron, M. A., 1991. The immature stages of Aegidium cribratum Bates (Coleoptera, Scarabaeidae, Orphninae). Coleopterists Bull. 45, 360 - 367.","Moron, M. A., Arce, R., 2003. Description of third instar larva and pupa of Ceratocanthus relucens (Bates) (Coleoptera: Scarabaeidae; Ceratocanthinae). Coleopterists Bull. 57, 245 - 253.","Reyes-Castillo, P., Martinez, A., 1979. Nuevos Rhyparini neotropicales, con notas sobre su biologia (Coleoptera, Scarabaeidae, Aphodiinae). Folia Entomologica Mexicana 41, 115 - 133.","Edmonds, W. D., 1967. The immature stages of Phanaeus (Coprophanaeus) jasius Olivier and Phanaeus (Metallophanaeus) saphirinus Sturm (Coleoptera: Scarabaeidae). Coleopterist Bull. 21, 97 - 105.","Lopez-Guerrero, Y., Moron, M. A., 1994. Description of immature stages of Eurysternus mexicanus Burmeister and Sisyphus submonticolus Howden (Coleoptera: Scarabaeidae: Scarabaeinae). J. Kansas Entomol. Soc. 67, 347 - 353.","Moron, M. A., 1993. Observaciones comparativas sobre la morfologia pupal de los Coleoptera Melolonthidae neotropicales. Giornale Italiano di Entomologia 6, 249 - 255."]}
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- 2015
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23. Record of Scarabaeoidea Larvae and Adults Associated withAmaranthus hypochondriacusL. and Living Fences
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Álvarez, Hugo A., primary, Carrillo-Ruiz, Hortensia, additional, and Morón, Miguel A., additional
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- 2016
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24. Abundance of Insect Fauna Associated with Amaranthus hypochondriacus L. Crop, in Relation to Natural Living Fences.
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Álvarez, Hugo A., Carrillo-Ruiz, Hortensia, Jiménez-García, Daniel, and Morón, Miguel A.
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AMARANTHS , *INSECT physiology , *CROP yields , *FENCES , *AGRICULTURAL ecology , *ECONOMICS , *EQUIPMENT & supplies - Abstract
Abundance of insect fauna associated with Amaranthus hypochondriacus L. in small-holder farm conditions, in terms of field complexity was studied. Agroecology theory suggests that natural fence rows reinforce good microclimatic conditions in a crop field, and provide food and cover for wildlife that could benefit the crop. However, organisms respond differently to the presence of an edge which could be positive or negative, and the response is driven by the form of the edge. In total, 1,621 specimens were collected in the insect orders Coleoptera, Diptera, Hymenoptera, Lepidoptera, Neuroptera, Orthoptera, the suborders Heteroptera, Homoptera, superfamily Mantodea, family Aleyrodidae, and class Arachnida. Results revealed that even when abundance of Heteroptera and Homoptera differ between sample areas of living fences, no fences, and natural vegetation, overall abundance was not related with field complexity. Response of arthropods to the presence of a natural living fence was neutral. However, tendencies in abundance suggested possible edge effects. [ABSTRACT FROM AUTHOR]
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- 2017
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25. New Records of Stagmomantis limbata1 for Three States of Central Mexico.
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Álvarez, Hugo A., Carrillo-Ruiz, Hortensia, Jiménez-García, Daniel, and Morón, Miguel A.
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STAGMOMANTIS , *MANTODEA , *FOREST plants , *PREDATORY insects , *GRASSLANDS - Abstract
The mantids of Mexico are not well known. We found records of Stagmomantis limbata Hahn for the states of Guerrero, Morelos, and Puebla, in central Mexico, and discuss the geographical range and weather variables in the recorded information. Results suggested that, at least S. limbata was found in deciduous forest, grassland, and cloudy forest vegetation in places with semi-warm to temperate climates throughout Balsas and Tuxpan-Nautla hydological regions. [ABSTRACT FROM AUTHOR]
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- 2017
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26. Horns positive allometry in a Mexican population of Strategus aloeus (L.) (Coleoptera: Scarabaeoidea: Dynastinae)
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Álvarez, Hugo A., Carrillo-Ruiz, Hortensia, Morón, Miguel Ángel, Álvarez, Hugo A., Carrillo-Ruiz, Hortensia, and Morón, Miguel Ángel
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The scaling relationships between horns and body size in a Mexican population of males of the rhinoceros beetle Strategus aloeus are analysed. We performed an allometric analysis using a sample of 94 specimens from many localities in Mexico. Our results suggest that median horn frequency in Strategus aloeus has a non-linear bimodal distribution and adjacent horns frequency has a non-linear distribution, however, residual and logarithmic transformation suggest linearity. Therefore we analysed data of horns using MA (model II) regression between log horns length and log body length; results of MA regression show strong positive allometry. These results suggest that bigger males possess larger disproportioned horns than small males, and that males could be investing more in developing the principal horn than in adjacent horns, possibly reflecting strong sexual pressures. This supports the idea that positive static allometry in horn and adjacent horns in S. aloeus could be explained by an extreme reaction norm, suggested by the “positive allometry reaction norm model”.
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- 2013
27. Record of Scarabaeoidea Larvae and Adults Associated with Amaranthus hypochondriacus L. and Living Fences.
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Álvarez, Hugo A., Carrillo-Ruiz, Hortensia, and Morón, Miguel A.
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AMARANTHS , *SCARABAEIDAE , *DECIDUOUS forests , *FENCES , *PHYLLOPHAGA - Abstract
White grubs of several species are known to plague crops such as amaranth. White grubs of the subfamily Melolonthinae significantly damage amaranth production. Agroecology theory suggests that natural fence rows provide food and cover for wildlife and help control soil erosion, which could help control plagues. However, there is no information regarding larvae and adults associated with amaranth crops in relation to natural fences. Here we record adults and larvae of Scarabaeoidea associated with Amaranthus hypochondriacus L. crop, adjacent to a deciduous forest and living fences. Results showed the occurrence of 12 species grouped in two families and seven genera. Phyllophaga obsoleta and P. ravida were the most abundant species. Larvae were collected in the growing area near the fence and in the natural zone. [ABSTRACT FROM AUTHOR]
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- 2016
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28. Comparative Study of the Reproductive System of Two Species of Hoplia (Coleoptera: Scarabaeidae: Hopliinae)
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Carrillo-Ruiz, Hortensia, primary, Imelda Martínez, M., additional, and Morón, Miguel A., additional
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- 2008
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29. Variaciones de la comunidad de visitadores florales de Bursera copallifera (Burseraceae) a lo largo de un gradiente de perturbación antropogénica.
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Rivas-Arancibia, Sombra Patricia, Bello-Cervantes, Eribel, Carrillo-Ruiz, Hortensia, Andrés-Hernández, Agustina Rosa, Figueroa-Castro, Dulce María, and Guzmán-Jiménez, Silvia
- Abstract
Copyright of Revista Mexicana de Biodiversidad is the property of Universidad Nacional Autonoma de Mexico, Instituto de Biologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2015
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30. FAUNA DE COLEOPTERA SCARABAEOIDEA DE CUETZALAN DEL PROGRESO, PUEBLA , MÉX ICO
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Carrillo Ruiz, Hortensia, primary and Morón Ríos, Miguel Ángel, additional
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- 2003
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31. Spatial Variation in the Community of Insects Associated with the Flowers of Pachycereus weberi (Caryophyllales: Cactaceae).
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Figueroa-Castro, Dulce María, Valverde, Pedro Luis, Vite, Fernando, and Carrillo-Ruiz, Hortensia
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INSECTS ,FLOWERS ,PESTS ,CACTUS ,PLANTS - Abstract
The positive relationship between productivity and species diversity is well-known. Insect communities associated with the flowers of Cactaceae species represent an interesting system to explore the productivity-diversity relationship because branches facing the equator receive more photosynthetically active radiation and have higher productivity. Thus, flowers with contrasting orientations within an individual, and even within a single branch, might differ in productivity. Therefore, higher abundance, species richness, and diversity are expected for the insect communities associated with south-facing flowers. This hypothesis was tested in Pachycereus weberi (J.M. Coulter) Backeberg (Cactaceae). Insects within flowers with contrasting orientations were collected and its abundance, richness, and diversity were estimated. We also asked if insects prefer big flowers. Thus, flower volume was estimated and regression analyses were conducted to test if there is a positive relationship between flower size and insect abundance. Flower orientation did not affect species richness. However, species abundance and diversity were different in flowers with contrasting orientations. In general, species abundance was higher in flowers facing southwards than in north-facing flowers. On the contrary, species diversity was higher in north-facing flowers. Abundance of Coleoptera was explained by flower volume in south-facing flowers. Contrary to our hypothesis, total diversity was greater in the less productive oriented flowers. Three possible explanations are discussed to explain the low diversity found in the highly productive, south-facing flowers. Our study provides evidence for the effects of productivity on the structure of insect communities at a very small-scale. [ABSTRACT FROM AUTHOR]
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- 2014
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32. Description of immature stages of Hoplia mexicanaHarold and H. squamiferaBurmeister (Coleoptera, Melolonthidae, Hopliinae)
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Morón, Miguel Ángel, Ramírez-Ponce, Andrés, Ramírez-Salinas, Concepción, and Carrillo-Ruiz, Hortensia
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Third stage larvae and pupae are described based on specimens collected in Mexico: Oaxaca (Cerro Zempoaltepetl), and Chiapas (Amatenango), respectively. Pupal characters are described for the first time for American Hopliinae. Habitus images and figures of diagnostic characters as well as comments on the differences between these larvae and those of Hoplia callipygeLeConte, 1856 and H. equinaLeConte, 1880, the only Hopliinae larvae previously known in New World, are also included.
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- 2016
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33. Variaciones de la comunidad de visitadores florales de Bursera copallifera(Burseraceae) a lo largo de un gradiente de perturbación antropogénica
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Patricia Rivas-Arancibia, Sombra, Bello-Cervantes, Eribel, Carrillo-Ruiz, Hortensia, Rosa Andrés-Hernández, Agustina, María Figueroa-Castro, Dulce, and Guzmán-Jiménez, Silvia
- Abstract
El cambio en las condiciones ambientales y el grado de perturbación antropogénica afectan las comunidades de visitadores florales. Así, se identificó y caracterizó la comunidad de visitadores florales de Bursera copallifera, en Jolalpan, Puebla, México, considerando cambios en variables ambientales (temperatura, humedad y altitud) y factores asociados con un gradiente de perturbación. Se usó un índice multimétrico cuantitativo para medir la perturbación en 13 zonas de la localidad. Se seleccionaron 3 sitios en un gradiente de perturbación, donde se recolectaron los visitantes florales. Se registró un total de 66 especies, pertenecientes a 25 familias, repartidas en 5 órdenes. Los órdenes con mayor abundancia fueron Hymenoptera y Coleoptera. La temperatura y la humedad fueron significativamente diferentes entre horarios y sitios, y en conjunto con los factores de perturbación, afectaron la estructura y dinámica de la comunidad de visitadores florales. El sitio más perturbado fue significativamente menos diverso, pero más abundante en insectos. Apis melliferafue la especie más abundante en el sitio más perturbado, aunque debido a la variación de altitud entre sitios, el efecto de la perturbación no fue claramente establecido. La gran diversidad de insectos encontrados mostraron la importancia de Bursera copalliferaen este tipo de ecosistemas.
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- 2015
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34. Patrones de distribución del género ZanthoxylumL. (Rutaceae) en México
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Puga-Jiménez, Ana Laura, Andrés-Hernández, Agustina Rosa, Carrillo-Ruiz, Hortensia, Espinosa, David, and Rivas-Arancibia, Sombra Patricia
- Abstract
El género Zanthoxylumtiene distribución pantropical y México es considerado un centro de diversificación para este género. Por tal motivo, se llevó a cabo un análisis de trazos con el programa Trazos 2004® y se realizaron 2 análisis de parsimonia de endemismos (PAE, por sus siglas en inglés), uno de áreas y otro con los tipos de vegetación donde habitan las especies. Se obtuvieron 21 trazos individuales y 2 trazos generalizados en la Zona de Transición Mexicana de Montaña y Neotropical. Se obtuvieron 3 nodos, 2 se ubican en la transición de las provincias de la Sierra Madre Oriental, Golfo de México y Oaxaca y el otro se ubica en la provincia del Golfo de México. El análisis de simplicidad de endemismos (PAE) agrupa a las provincias de la Costa del Pacífico, el Eje Neovolcánico, el Golfo de México, Oaxaca, Depresión del Balsas y la Sierra Madre del Sur, en un conjunto de clados sucesivamente anidados, sustentados por Zanthoxylum aguilarii, Z. culantrillo, Z. liebmannianumy Z. purpusiien diferentes ramas. Con el análisis de vegetación se obtuvo un cladograma, en donde los tipos de vegetación de las zonas templadas (bosque mesófilo de montaña, bosque de Quercusy Coníferas) forman un clado reciente sustentado por Z. elegantissimum, Z. foliolosumy Z. melanorhachis.
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- 2013
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