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1

Sekerka, Lukáš. "Taxonomic changes within Imatidiini and Hybosispini (Coleoptera: Chrysomelidae: Cassidinae)." Acta Entomologica Musei Nationalis Pragae 57, no. 2 (2017): 351–80. http://dx.doi.org/10.1515/aemnp-2017-0081.

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Type specimens of various taxa of Imatidiini and Hybosispini were examined to verify their identity. The following taxonomic changes are proposed based on these comparisons. New combinations: Cephaloleia apertura (Staines, 2013) comb. nov. (from Aslamidium Borowiec, 1984), Cephaloleia jataiensis (Pic, 1923) comb. nov. (from Xenispa Baly, 1859), Pseudimatidium bicoloricornis (Pic, 1926) comb. nov. (from Windsorispa Sekerka, 2014), Xanthispa miniacea (Blanchard, 1843) comb. nov. (from Homalispa Baly, 1859), Xenispa aeneipennis (Baly, 1859) comb. nov. (from Cephaloleia Chevrolat, 1836), Xenispa gilvipes (Uhmann, 1930) comb. nov. (from Cephaloleia), Hybosispa claripes (Pic, 1923) comb. nov. (from Solenispa Weise, 1905), Hybosispa delectabilis (Staines, 1996) comb. nov. (from Cephaloleia), Hybosispa sulciceps (Baly, 1885) comb. nov. (from Cephaloleia), and Hybosispa truncatipennis (Baly, 1869) comb. nov. (from Cephaloleia). New synonyms: Cephaloleia impressa Uhmann, 1930 = Demothispa clermonti Pic, 1934 syn. nov.; Xenispa atra (Pic, 1926) = Cephaloleia cyanea Staines, 1996, syn. nov. Change in status: Cephaloleia fernandoi (Bondar, 1940) stat. restit. is removed from synonymy with C. opaca Baly, 1859. The monotypic genus Serratispa Staines, 2002 assign. nov. is transferred from Sceloenoplini to Imatidiini based on morphological characters. Three species are described: Cephaloleia fouquei sp. nov. from Bolivia and Peru, C. renei sp. nov. from Ecuador, and Xenispa fouquei sp. nov. from Venezuela. Keys to Cephaloleia basalis Weise, 1910 species-group, Venezuelan species of Xenispa Baly, 1859, and species of Hybosispa Weise, 1905 are proposed to simplify identifi cation of respective taxa. Most of the taxa discussed herein are provided with colour photographs.
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2

Garcia-Robledo, Carlos, Charles L. Staines, and W. John Kress. "A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets." ZooKeys 477 (January 26, 2015): 143–55. https://doi.org/10.3897/zookeys.477.8220.

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The Neotropical genus Cephaloleia Chevrolat (Coleoptera: Chrysomelidae: Cassidinae) includes 214 species distributed from the south of Mexico to Argentina. Cephaloleia beetles feed mostly on plants from the order Zingiberales. The interactions between Cephaloleia beetles and their Zingiberales host plants is proposed as one of the oldest and most conservative associations. Here we describe a new species of Cephaloleia (C. kuprewiczae sp. n.) that feeds on two species of bromeliads (Pitcairnia arcuata and P. brittoniana, Bromeliaceae: Pitcairnioideae). Cephaloleia kuprewiczae was previously described as Cephaloleia histrionica. This study includes evidence from DNA barcodes (COI), larval and adult morphology and insect diets that separates C. kuprewiczae from C. histrionica as a new species.
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3

GARCÍA-ROBLEDO, CARLOS, CAROL C. HORVITZ, and CHARLES L. STAINES. "Larval morphology, development, and notes on the natural history of Cephaloleia “rolled-leaf” beetles (Coleoptera: Chrysomelidae: Cassidinae)." Zootaxa 2610, no. 1 (2010): 50. http://dx.doi.org/10.11646/zootaxa.2610.1.3.

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The Neotropical genus Cephaloleia Chevrolat, 1837 is comprised of 209 described species. Adults usually feed and mate within the scrolls formed by the young rolled leaves of plants of Neotropical Zingiberales. This paper reports for populations of Cephaloleia belti Baly, C. dilaticollis Baly, C. dorsalis Baly and C. placida Baly at La Selva Biological Station (Costa Rica, Central America) detailed descriptions of: 1. larval and adult diets and diet breadth; 2. egg, larval and pupal morphology; 3. larval development times; 4. dimorphic sexual characteristics; 5. adult longevity; and 6. differences in lifespan between genders. Cephaloleia belti displays the broader diet breadth, feeding on 14 species of three families of Zingiberales. Cephaloleia dilaticollis feeds on nine species of three families of Zingiberales. Cephaloleia dorsalis and C. placida feed on four species of Costaceae and two species of Zingiberaceae, respectively. Time to pupation ranges among species from 32.8 to 59.1 days. In the four Cephaloleia species, adult females are larger than males. Genders display marked sexual dimorphism in the shape of their last abdominal sternite and the pygidium. Longevity of adults ranged from ca. 300 to 390 days. Life expectancy estimates for adult beetles reared in the laboratory ranged from 111.5 to 187.2 days. Male and female adults of C. belti and C. dilaticollis have equivalent life expectancies. However, life expectancy is longer for male C. dorsalis and C. placida.
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4

Barrios-Trilleras, Carlos Enrique, Natalia Julieth Castillo-Villarraga, Alex Enrique Bustillo-Pardey, and Charles L. Staines. "Nuevos registros de Cephaloleia (Coleoptera: Chrysomelidae) plaga de la palma de aceite en Colombia." Revista Colombiana de Entomología 46, no. 1 (2020): e6863. http://dx.doi.org/10.25100/socolen.v46i1.6863.

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Se confirmó la identidad taxonómica de Cephaloleia vagelineata y se registra por primera vez en Colombia la especie Cephaloleia depressa y que causa daños en plantaciones de palma de aceite. También, se ofrece un reconocimiento morfológico de los adultos de ambas especies para facilitar su identificación.
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5

Blankenchip, Chelsea L., Dana E. Michels, H. Elizabeth Braker, and Shana K. Goffredi. "Diet breadth and exploitation of exotic plants shift the core microbiome of Cephaloleia, a group of tropical herbivorous beetles." PeerJ 6 (May 17, 2018): e4793. http://dx.doi.org/10.7717/peerj.4793.

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The beetle genus Cephaloleia has evolved in association with tropical ginger plants and for many species their specific host plant associations are known. Here we show that the core microbiome of six closely related Costa Rican Cephaloleia species comprises only eight bacterial groups, including members of the Acinetobacter, Enterobacteriacea, Pseudomonas, Lactococcus, and Comamonas. The Acinetobacter and Enterobacteriacea together accounted for 35% of the total average 16S rRNA ribotypes recovered from all specimens. Further, microbiome diversity and community structure was significantly linked to beetle diet breadth, between those foraging on less than two plant types (specialists) versus over nine plant types (generalists). Moraxellaceae, Enterobacteriaceae, and Pseudomonadaceae were highly prevalent in specialist species, and also present in eggs, while Rickettsiaceae associated exclusively with generalist beetles. Bacteria isolated from Cephaloleia digestive systems had distinct capabilities and suggested a possible beneficial role in both digestion of plant-based compounds, including xylose, mannitol, and pectin, and possible detoxification, via lipases. Cephaloleia species are currently expanding their diets to include exotic invasive plants, yet it is unknown whether their microbial community plays a role in this transition. In this study, colonization of invasive plants was correlated with a dysbiosis of the microbiome, suggesting a possible relationship between gut bacteria and niche adaptation.
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6

Staines, Charles L., and Carlos Garcia-Robledo. "The genus Cephaloleia Chevrolat, 1836 (Coleoptera, Chrysomelidae, Cassidinae)." ZooKeys 436 (August 22, 2014): 1–355. https://doi.org/10.3897/zookeys.436.5766.

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The species of the Neotropical genus <em>Cephaloleia </em>Chevrolat, 1836 are revised. We present a key to the known larvae of <em>Cephaloleia </em>(8 species), a key to the 95 species known to occur in Mexico, Central America and the West Indies, and a key to the 138 species known to occur in South America. All identification keys were translated to Spanish. Descriptions for the 214 known species of <em>Cephaloleia </em>as well as illustrations for 212 species are presented. The following species are removed from <em>Cephaloleia</em>: <em>C. bipartita </em>Pic, 1926c is transferred to <em>Hybosispa</em> Weise, 1910; <em>C. minasensis </em>Pic, 1931 and <em>C. viridis </em>Pic, 1931 are transferred to <em>Stenispa </em>Baly, 1858. The following species are described as new: <em>C. abdita</em> <strong>sp. n.</strong> from Brazil; <em>C. amba </em><strong>sp. n.</strong> from Colombia, Ecuador, and Peru; <em>C. angustacollis </em><strong>sp. n.</strong> from Ecuador; <em>C. brevis </em><strong>sp. n.</strong> from French Guiana; <em>C. calathae </em><strong>sp. n.</strong> from Costa Rica; <em>C. chica </em><strong>sp. n.</strong> from Peru; <em>C. conforma </em><strong>sp. n.</strong> from Costa Rica; <em>C. crenulata </em><strong>sp. n.</strong> from Ecuador; <em>C. gemma </em><strong>sp. n.</strong> from Bolivia and Brazil; <em>C. horvitzae </em><strong>sp. n.</strong> from French Guiana; <em>C. interrupta </em><strong>sp. n.</strong> from Costa Rica; <em>C. kressi </em><strong>sp. n.</strong> from Costa Rica; <em>C. lenticula </em><strong>sp. n.</strong> from Ecuador, French Guiana, Peru, and Suriname; <em>C. nana </em><strong>sp. n.</strong> from Ecuador; <em>C. ochra </em><strong>sp. n.</strong> from Ecuador; <em>C. stainesi </em><strong>sp. n.</strong> from Costa Rica; and <em>C. susanae </em><strong>sp. n.</strong> from Brazil and Ecuador. <em>Cephaloleia simoni </em>Pic, 1934 is treated as Incertae sedis. The larvae of <em>C. erichsonii </em>Baly, 1858 and <em>C. puncticollis </em>Baly, 1885 are described and illustrated.
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7

Staines, C. L. "A new species of Cephaloleia Chevrolat, 1837 (Coleoptera: Chrysomelidae: Cassidinae) from Dominica." Insecta Mundi 2008, no. 30 (2008): 1–4. https://doi.org/10.5281/zenodo.4532893.

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8

García-Robledo, Carlos, Carol C. Horvitz, and Charles L. Staines. "Larval morphology, development, and notes on the natural history of Cephaloleia " rolled-leaf " beetles (Coleoptera: Chrysomelidae: Cassidinae)." Zootaxa 2610 (December 31, 2010): 50–68. https://doi.org/10.5281/zenodo.197794.

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García-Robledo, Carlos, Horvitz, Carol C., Staines, Charles L. (2010): Larval morphology, development, and notes on the natural history of Cephaloleia " rolled-leaf " beetles (Coleoptera: Chrysomelidae: Cassidinae). Zootaxa 2610: 50-68, DOI: 10.5281/zenodo.197794
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9

Sekerka, Lukáš, Donald Windsor, and Charles L. Staines. "A new species of Cephaloleia from Panama with description of larva and first record of orchid-feeding in Cephaloleiini (Coleoptera: Chrysomelidae: Cassidinae)." Acta Entomologica Musei Nationalis Pragae 53, no. 1 (2013): 303–14. https://doi.org/10.5281/zenodo.5740509.

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Sekerka, Lukáš, Windsor, Donald, Staines, Charles L. (2013): A new species of Cephaloleia from Panama with description of larva and first record of orchid-feeding in Cephaloleiini (Coleoptera: Chrysomelidae: Cassidinae). Acta Entomologica Musei Nationalis Pragae 53 (1): 303-314, DOI: 10.5281/zenodo.5740509
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10

Schmitt, Michael, and Meike Frank. "Notes on the ecology of rolled-leaf hispines (Chrysomelidae, Cassidinae) at La Gamba (Costa Rica)." ZooKeys 332 (September 19, 2013): 55–69. https://doi.org/10.3897/zookeys.332.5215.

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A total of 301 adult hispine beetles of the genera <i>Cephaloleia</i> and <i>Chelobasis</i> were found in rolled leaves of plants of 17 species of Zingiberales (families Costaceae, Heliconiaceae, Maranthaceae, Musaceae, and Zingiberaceae) during a field study at La Gamba, Golfito region, Costa Rica. Of these beetles, <i>Cephaloleia belti</i> was recorded from 12 potential host plant species, <i>C. distincta from </i>7, <i>C.</i> <i>dilaticollis</i> from 5, <i>C.</i>, <i>Chelobasis bicolor</i>, <i>C. championi,</i> and <i>C. histrionica </i>from 3, <i>Chelobasis perplexa</i> and <i>C.</i> <i>instabilis</i> from 2, whereas <i>C. trivittata </i>from only one. Of the plant species, <i>Heliconia latispatha</i> had 7 beetle species in its leaf rolls, <i>Calathea lutea</i> had 5, <i>H. imbricata</i> and <i>H. rostrata</i> had 4, <i>H. stricta</i> and <i>Musa paradisiaca</i> had 3, <i>H. wagneriana</i> had 2, while on <i>H. vaginalis</i>, <i>H. danielsiana</i>, <i>H. densiflora</i>, <i>H. longiflora</i>, <i>Calathea crotalifera</i>, <i>C.</i> <i>platystachya</i>, <i>Goeppertia lasiophylla</i>, <i>Alpinia purpurata</i>, <i>Costus pulverulentus</i> and <i>Costus barbatus</i>, <i>H. densiflora</i>, <i>H. vaginalis</i>, and <i>H. danielsana</i> only hispines of one species were found.<i>Cephaloleia belti</i> occurred together with beetles of six other hispine species, whereas <i>Cephaloleia</i> <i>trivittata</i> never shared a leaf roll with another hispine species. The remaining beetle species aggregated with one to four other hispines. Adults of <i>C. belti</i> and <i>C. championi</i> were frequently seen, occasionally also with <i>C. dilaticollis, C. histrionica, and Chelobasis perplexa</i>, to co-occur with the carabid <i>Calophaena ligata</i> in the same leaf roll without any sign of interspecific aggression.A comparison of host choices and the phylogeny of the hispines and of their host plants revealed no signs that beetles used species level phylogenetic relationships within the Zingiberales to food plants. Obviously, within this plant order, rolled-leaf hispines choose their plant hosts in a nearly opportunistic manner. Seemingly, they use differences among plants at higher taxonomic levels but within the Zingiberales, the availability of young – rolled – leaves might be the actual decisive factor.
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11

Staines, Charles L., and Carlos Garcia-Robledo. "The genus Cephaloleia Chevrolat, 1836 (Coleoptera, Chrysomelidae, Cassidinae)." ZooKeys 436 (August 22, 2014): 1–355. http://dx.doi.org/10.3897/zookeys.436.5766.

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12

Chaves-Fallas, José Miguel. "Predation of the Rolled-Leaf Beetle Cephaloleia kressi García-Robledo (Coleoptera: Chrysomelidae: Cassidinae) by the Rove Beetle Phanolinus Sp. (Coleoptera: Staphylinidae: Xanthopygina) in a Montane Forest of Costa Rica." Coleopterists Bulletin 74, no. 4 (2020): 714–18. https://doi.org/10.1649/0010-065X-74.4.714.

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Chaves-Fallas, José Miguel (2020): Predation of the Rolled-Leaf Beetle Cephaloleia kressi García-Robledo (Coleoptera: Chrysomelidae: Cassidinae) by the Rove Beetle Phanolinus Sp. (Coleoptera: Staphylinidae: Xanthopygina) in a Montane Forest of Costa Rica. The Coleopterists Bulletin 74 (4): 714-718, DOI: 10.1649/0010-065X-74.4.714, URL: http://dx.doi.org/10.1649/0010-065x-74.4.714
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13

ERWIN, TERRY L., and RAUL F. MEDINA. "The Neotropical species Askalaphium depressum (Bates): Larval description, first diagnosis and illustrations of immature Ctenodactylini, with natural history notes on the genus and tribe (Coleoptera: Carabidae)." Zootaxa 273, no. 1 (2003): 1. http://dx.doi.org/10.11646/zootaxa.273.1.1.

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Adults and larvae of Askalaphium depressum (Bates) live in association with hispine chrysomelid beetles of the genus Cephaloleia Chevrolat, in the appressed leaf axils of the riverside reed, Gynerium sagittatum (Aubl.) P. Beauv. This reed is locally known in Amazonian Perú as Caña Brava. Both adult and larval A. depressum eat larvae of Cephaloleia species and larvae of an unidentified dipteran, and perhaps other insects living in the confines of the leaf sheaths of that plant species. The geographic range of Caña Brava reed extends from subtropical South America northward to México (and Florida), but A. depressum has been found thus far at only three Amazonian localities, probably indicating its cryptic microhabitat and lack of collecting, therein. Likely, the range of this commensal carabid species is more extensive and may approach the range of its host plant and hispine food. Structural features of second and third instar larvae of A. depressum are described for the first time. Larval character states that are shared with a related ctenodactyline, Leptotrachelus dorsalis (Fabricius), provide a basis for characterization of the tribe Ctenodactylini.
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14

Johnson, Derek Marley. "Life History and Demography of Cephaloleia fenestrata (Hispinae: Chrysomelidae: Coleoptera)." Biotropica 36, no. 3 (2004): 352–61. http://dx.doi.org/10.1111/j.1744-7429.2004.tb00327.x.

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15

Johnson, Derek Marley. "Life History and Demography of Cephaloleia fenestrata (Hispinae: Chrysomelidae: Coleoptera)1." BIOTROPICA 36, no. 3 (2004): 352. http://dx.doi.org/10.1646/03069.

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16

Arreguín-Espinosa, Roberto, Barbarín Arreguín, and Carolina González. "Purification and properties of a lipase from Cephaloleia presignis (Coleoptera, Chrysomelidae)." Biotechnology and Applied Biochemistry 31, no. 3 (2000): 239. http://dx.doi.org/10.1042/ba19990088.

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17

Moraza, Maria L., and Evert E. Lindquist. "A new species-group with new species of the genus Lasioseius (Acari: Mesostigmata: Blattisociidae) associated with neotropical hispine beetles in furled leaves of Heliconia." Acarologia 58, no. 1 (2018): 62–98. http://dx.doi.org/10.24349/acarologia/20184227.

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A new species-group of Lasioseius is described from adults and immatures of four newly described and one undescribed species associated with hispine beetles of the genera Cephaloleia and Chelobasis and other gamasine mites in the furled leaf habitat of Heliconia and related Zingiberales plants. The species-group presents a suite of apomorphic attributes placing it in the subgenus L. (Lasioseius). Adults and immatures were found moving freely on and off the beetles when the latter were exposed from their habitat. Larviparity is indicated by adult females gravid with fully developed larvae. Limited data suggest considerable host specificity between mites and their beetle hosts, indicating that there may be a vast diversity of these mites associated with hundreds of species of hispine beetles in the Neotropical Region. Keys are provided to currently accepted species-groups of Lasioseius and to the species within the new species-group.
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18

McKenna, Duane D., and Brian D. Farrell. "Molecular phylogenetics and evolution of host plant use in the Neotropical rolled leaf ‘hispine’ beetle genus Cephaloleia (Chevrolat) (Chrysomelidae: Cassidinae)." Molecular Phylogenetics and Evolution 37, no. 1 (2005): 117–31. http://dx.doi.org/10.1016/j.ympev.2005.06.011.

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19

Garcia-Robledo, Carlos, Charles L. Staines, and W. John Kress. "A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets." ZooKeys 477 (January 26, 2015): 143–55. http://dx.doi.org/10.3897/zookeys.477.8220.

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20

Moraza, Maria L., and Evert E. Lindquist. "New species and biological data for the neotropical mite genus Hispiniphis (Acari: Mesostigmata: Melicharidae) associated with hispine beetles, genus Cephaloleia, in unfurled leaves of Heliconia." Systematic and Applied Acarology 21, no. 1 (2016): 85. http://dx.doi.org/10.11158/saa.21.1.7.

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21

"Cephaloleia neglecta." CABI Compendium CABI Compendium (January 7, 2022). http://dx.doi.org/10.1079/cabicompendium.119731.

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22

Del Rivero Bautista, Nydia, Egla Lugo-Cruz, Saúl Sánchez-Soto, Rodolfo Osorio- Osorio, and Jesús Romero-Nápoles. "INSECTOS FITÓFAGOS ASOCIADOS A CULTIVOS DE HELICONIAS (Heliconia spp.) EN TABASCO, MÉXICO." AgroProductividad 13, no. 2 (2020). http://dx.doi.org/10.32854/agrop.vi.1582.

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RESUMEN&#x0D; Objetivo: Identificar las especies de insectos que se alimentan y dañan plantas del género Heliconia (Heliconiaceae) en plantaciones comerciales del estado de Tabasco, México.&#x0D; Diseño/metodología/aproximación: De enero a octubre de 2013 se visitaron quincenalmente tres plantaciones en los municipios de Cárdenas, Comalcalco y Teapa, para detectar insectos fitófagos.&#x0D; Resultados: Se identificaron cuatro especies de insectos pertenecientes a tres órdenes y tres familias: Cephaloleia sallei (Coleoptera: Chrysomelidae) asociada a H. psittacorum, Cephaloleia vicina (Coleoptera: Chrysomelidae) asociada a H. latisphata, Pentalonia sp. (Hemiptera: Aphididae) asociada a H. latisphata, y Telchin atymnius futilis (Lepidoptera: Castniidae) asociada a H. psittacorum, H. bihai y H. stricta.&#x0D; Limitaciones/implicaciones: Pentalonia sp. no se pudo registrar a nivel de especie. Para ello se sugiere un estudio que tome en cuenta áfidos de este género recolectados también en plantas de plátano (Musa spp.) y otras hospederas.&#x0D; Hallazgos/conclusiones: Fueron pocas las especies de insectos que se encontraron alimentándose o dañando heliconias cultivadas; sin embargo, se considera que estos insectos tienen potencial para afectar el cultivo o el producto destinado como flor de corte.
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23

Sekerka, Lukáš. "Commented catalogue of Cassidinae (Coleoptera: Chrysomelidae) of the state of São Paulo, Brazil, with remarks on the collection of Jaro Mráz in the National Museum in Prague." Acta Entomologica Musei Nationalis Pragae, December 26, 2020, 667–707. http://dx.doi.org/10.37520/aemnp.2020.048.

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Commented catalogue of Cassidinae species reported from the state of São Paulo, Brazil is given. Altogether, 343 species are presently registered from the state representing the following tribes: Alurnini (5 spp.), Cassidini (84 spp.), Chalepini (85 spp.), Dorynotini (9 spp.), Goniocheniini (8 spp.), Hemisphaerotini (2 spp.), Imatidiini (25 spp.), Ischyrosonychini (6 spp.), Mesomphaliini (83 spp.), Omocerini (14 spp.), Sceloenoplini (9 spp.), and Spilophorini (13 spp.). Fifty-two species are recorded for the first time and 19 are removed from the fauna of São Paulo. Each species is provided with a summary of published faunistic records for São Paulo and its general distribution. Dubious or insufficient records are critically commented. A list of Cassidinae species collected in São Paulo by Jaro Mráz (altogether 145 identified species) is included and supplemented with general information on this material. In addition, two new synonymies are established: Cephaloleia caeruleata Baly, 1875 = C. dilatata Uhmann, 1948, syn. nov.; Stolas lineaticollis (Boheman, 1850) = S. silaceipennis (Boheman, 1862), syn. nov.; and the publication year of the genus Heptatomispa Uhmann, 1940 is corrected to 1932. The following 54 species are recorded from São Paulo for the first time: Agroiconota tristriata (Fabricius, 1792), Charidotella (Philaspis) polita (Klug, 1829), Charidotis admirabilis Boheman, 1855, C. auroguttata Boheman, 1855, C. circumscripta Boheman, 1855, C. concentrica (Boheman, 1855), C. consentanea (Boheman, 1855), C. gemellata Boheman, 1855, Coptocycla (s. str.) stigma (Germar, 1823), Coptocycla (Coptocyclella) adamantina (Germar, 1823), Eremionycha bahiana (Boheman, 1855), Helocassis flavorugosa (Boheman, 1855), Helocassis flavorugosa (Boheman, 1855), Microctenochira patruelis (Boheman, 1855), Plagiometriona deyrollei (Boheman, 1855), P. punctatissima (Boheman, 1855), P. tenella (Klug, 1829), Baliosus conspersus Weise, 1911, Chalepus aenescens Weise, 1910, Decatelia pallipes (Weise, 1922), Octhispa gemmata (Germar, 1823), Octhispa robinsonii (Baly, 1864), Octotoma brasiliensis Weise, 1921, Octotoma crassicornis Weise, 1910, Oxychalepus centralis Uhmann, 1940, Temnochalepus imitans Uhmann, 1935, Uroplata coarctata Weise, 1921, Uroplata minuscula (Chapuis, 1877), Calliapis umbonata Hincks, 1956, Cephaloleia caeruleata Baly, 1875, C. flavovittata Baly, 1859, C. trilineata Uhmann, 1942, C. zikani Uhmann, 1935, Stenispa vespertina Baly, 1877, S. viridis (Pic, 1931), Xenispa bicolorata (Uhmann, 1948), Anacassis candida (Boheman, 1854), Chelymorpha commutabilis Boheman, 1854, C. constellata (Klug, 1829), Cyrtonota vulnerata (Boheman, 1850), Hilarocassis evanida (Boheman, 1850), Mesomphalia gibbosa (Fabricius, 1781), Nebraspis corticina (Boheman, 1850), Sceloenopla rectelineata (Pic, 1929), Stolas acuta (Boheman, 1850), S. aenea (Olivier, 1790), S. sexsignata (Boheman, 1850), S. sommeri (Boheman, 1850), S. subreticulata (Boheman, 1850), Omocerus (Platytauroma) cornutus (Boheman, 1850), Calyptocephala nigricornis (Germar, 1823), Oediopalpa brunnea (Uhmann, 1943), O. caerulescens (Baly, 1875), and O. fulvipes Baly, 1859.
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Chaves‐Fallas, José Miguel, Carlos García‐Robledo, Mónica M. Carlsen, Orlando Vargas, Mónica Rojas‐Gómez, and Robert J. Marquis. "The impact of host biogeography, ecology, evolutionary history, and architecture on the structure of rolled‐leaf beetle assemblages of Costa Rican Zingiberales." Biotropica 57, no. 1 (2025). https://doi.org/10.1111/btp.13402.

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AbstractDetermining the factors affecting the structure of insect herbivore communities is a major challenge in ecology. Previous research demonstrated that plant defenses determine plant‐herbivore associations. However, non‐defensive variables may also explain why some plant species are associated with more diverse insect herbivore assemblages than others. Neotropical rolled‐leaf beetles (Cephaloleia and Chelobasis) complete their life cycle inside the young rolled leaves of their host plants in the order Zingiberales. The diet breadth of each species in this assemblage is particularly well‐known at our study site, La Selva Biological Station in Costa Rica. This study focused on the following non‐defensive variables: host plant elevational and geographic range size, soil type, habitat, local abundance, plant size, and leaf size. Because plant characteristics among closely related plants are not independent, we analyzed these variables in a phylogenetic context. We detected a positive effect of leaf width on rolled‐leaf beetle species richness (explaining 55% of the variation), abundance (28% of the variation and 57% when habitat is included in the model), diversity (37% of the variation), and community structure (6% of the variation, and 21%–26% when taxonomic family is included in the model). Our study demonstrates that Zingiberales leaf width influences positively rolled‐leaf beetle species richness, abundance, and diversity. This effect varies among plant families. Our study shows that plant architecture plays an important role in structuring insect herbivore assemblages in Zingiberales. Our results highlight the importance of including variables beyond plant defenses to understand the ecology and evolution of plant‐herbivore interactions.
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25

Chaves-Fallas, José Miguel. "Predation of the Rolled-Leaf Beetle Cephaloleia kressi García-Robledo (Coleoptera: Chrysomelidae: Cassidinae) by the Rove Beetle Phanolinus Sp. (Coleoptera: Staphylinidae: Xanthopygina) in a Montane Forest of Costa Rica." Coleopterists Bulletin 74, no. 4 (2020). http://dx.doi.org/10.1649/0010-065x-74.4.714.

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