PUBLICATIONS TO BE ADDED Updated: August 6, 2021

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Diet of two sympatric insectivores bats (Chiroptera: Vespertilionidae) in the Cerrado of Central Brazil. Revista Brasileira de Zoologia, 25(1), 28–31 6. Aguiar, L. M. d. S., & Marinho-Filho, J. (2007). Bat frugivory in a remnant of Southeastern Brazilian Atlantic forest. Acta Chiropterologica, 9(1), 251-260. https://doi.org/10.3161/1733-5329(2007)9[251:BFIARO]2.0.CO;2 7. Aguilar-Rodríguez, P. A., MacSwiney G, M. C., Krömer, T., García-Franco, J. G., Knauer, A., & Kessler, M. (2014). First record of bat-pollination in the species-rich genus (Bromeliaceae). Annals of Botany, 113(6), 1047- 1055. https://doi.org/10.1093/aob/mcu031 8. Ahmim, M., & Moali, A. (2011). The diet of the Maghrebian mouse-eared bat Myotis punicus (Mammalia, Chiroptera) in Kabylia, Northern Algeria. Ecologia Mediterranea, 37(1), 45-51. 9. Ahmim, M., & Moali, A. (2013). The diet of four species of horseshoe bat (Chiroptera: Rhinolophidae) in a mountainous region of Algeria: evidence for gleaning. Hystrix, 24(2), 174-176. 10. Aihartza, J. R., Goiti, U., Almenar, D., & Garin, I. (2003). Evidences of Piscivory by Myotis capaccinii (Bonaparte, 1837) in Southern Iberian Peninsula. Acta Chiropterologica, 5(2), 193-198. 11. Aizpurua, O., Budinski, I., Georgiakakis, P., Gopalakrishnan, S., Ibanez, C., Mata, V., . . . Alberdi, A. (2018). Agriculture shapes the trophic niche of a bat preying on multiple pest arthropods across Europe: Evidence from DNA metabarcoding. Molecular Ecology, 27(3), 815-825. https://doi.org/10.1111/mec.14474 12. Aizpurua, O., Garin, I., Alberdi, A., Salsamendi, E., Baagøe, H., & Aihartza, J. (2013). Fishing Long-Fingered Bats (Myotis capaccinii) Prey Regularly upon Exotic Fish. PLoS One, 8(11). https://doi.org/10.1371/journal.pone.0080163 13. Albayrak, I., Aşan, N., & Yorulmaz, T. (2008). The Natural History of the Egyptian Fruit Bat, Rousettus aegyptiacus, in Turkey (Mammalia: Chiroptera). TURKISH JOURNAL OF ZOOLOGY, 32(1), 11-18. 14. Alberdi, A., Garin, I., Aizpurua, O., & Aihartza, J. (2012). The Foraging Ecology of the Mountain Long-Eared Bat Plecotus macrobullaris Revealed with DNA Mini-Barcodes. PLoS One, 7(4), Article e35692. https://doi.org/10.1371/journal.pone.0035692 15. Alcorn, S. M., McGregor, S. E., & Olin, G. (1961). Pollination of saguaro cactus by doves, nectar-feeding bats and honey bees. Science, 133, 1594-1595. 16. Alcorn, S. M., McGregor, S. E., & Olin, G. (1962). Pollination requirements of the organ pipe cactus. Cactus and Succulent Journal of the Cactus and Succulent Society of America, 34(4), 134-138. 17. Aldridge, H. D. J. N., & Rautenbach, I. L. (1987). Morphology, Echolocation and Resource Partitioning in Insectivorous Bats. Journal of Animal Ecology, 56(3), 763-778. https://doi.org/10.2307/4947 18. Allen, J. A., Lang, H., & Chapin, J. P. (1917). Article XVIII.- The American Museum Congo Expedition Collection of Bats. Bulletin American Museum of Natural History, 37, 405-563. 19. Alonso-Mejía, A., & Medellín, R. A. (1991). Micronycteris megalotis. Mammalian Species, 376, 1-6. 20. Alvarez, J., Willig, M. R., Jones, J. K., Jr., & Webster, W. D. (1991). Glossophaga soricina. Mammalian Species, 379, 1-7. 21. Alvarez, T., & Gonzales Quintero, L. (1969). Analisis polinico del contenido gastrico de murcielagos Glossophaginae de Mexico. Anales de la Escuela Nacional de Ciencias Biologicas, 18(1-4), 137-165. 22. Alvarez, T., & Sánchez-Casas, N. (1997). Notas sobre la alimentación de Musonycteris y Choeroniscus (Mammalia: Phyllostomidae) en México. Revista Mexicana de Mastozoología, 2, 113-115. 23. Amerson, A. B. J., Whistler, W. A., & Schwaner, T. D. (1982). Wildlife and Wildlife Habitat of American Samoa. 11. Accounts of Flora and Fauna (R. C. Banks, Ed. Vol. 2). U.S. Fish and Wildlife Service. 24. Ancillotto, L., Mazza, G., Menchetti, M., & Mori, E. (2014). Host specificity of the badger's flea (Paraceras melis) and first detection on a bat host. Parasitology Research, 113(10), 3909-3912. https://doi.org/10.1007/s00436- 014-4136-x 25. Andersen, K. (1912). Catalogue of the Chiroptera in the collection of the British Museum (2nd ed., Vol. 1). British Museum of Natural History. 26. Andrade, T. Y., Thies, W., Rogeri, P. K., Kalko, E. K. V., & Mello, M. A. R. (2013). Hierarchical fruit selection by Neotropical leaf-nosed bats (Chiroptera: Phyllostomidae). Journal of Mammalogy, 94(5), 1094- 1101. https://doi.org/10.1644/12-MAMM-A-244.1 27. Andreas, M., Reiter, A., & Benda, P. (2012a). Dietary composition, resource partitioning and trophic niche overlap in three forest foliage-gleaning bats in Central Europe. Acta Chiropterologica, 14(2), 335- 345. https://doi.org/http://dx.doi.org/10.3161/150811012X661657 28. Andreas, M., Reiter, A., & Benda, P. (2012b). Prey selection and seasonal diet changes in the western barbastelle bat Barbastella barbastellus. Acta Chiropterologica, 14(1), 81- 92. https://doi.org/http://dx.doi.org/10.3161/150811012X654295 29. Andriafidison, D., Andrianaivoarivelo, R. A., Ramilijaona, O. R., Razanahoera, M. R., Mackinnon, J., Jenkins, R. K. B., & Racey, P. A. (2006). Nectarivory by Endemic Malagasy Fruit Bats During the Dry Season. Biotropica, 38(1), 85-90. https://doi.org/10.1111/j.1744-7429.2006.00112.x 30. Andriafidison, D., Kofoky, A., Mbohoahy, T., Racey, P. A., & Jenkins, R. K. B. (2007). Diet, reproduction and roosting habits of the Madagascar free-tailed bat, Otomops madagascariensis Dorst, 1953 (Chiroptera: Molossidae) [research-article]. Acta Chiropterologica, 9, 445-450. https://doi.org/i1733-5329-9-2-445 31. Andrianaivoarivelo, R. A., Ramilijaona, O. R., Racey, P. A., Razafindrakoto, N., & Jenkins, R. K. B. (2011). Feeding ecology, habitat use and reproduction of Rousettus madagascariensis Grandidier, 1928 ( Chiroptera: Pteropodidae) in eastern Madagascar. Mammalia, 75(1), 69-78. https://doi.org/10.1515/mamm.2010.071 32. Andrianaivoarivelo, R. A., Ranaivoson, N., Racey, P. A., & Jenkins, R. K. B. (2006). The diet of three synanthropic bats (Chiroptera: Molossidae) from eastern Madagascar [research-article]. Acta Chiropterologica, 8(2), 439- 444. https://doi.org/i1733-5329-8-2-439 33. Aranguren, C. I., González-Carcacía, J. A., Martínez, H., & Nassar, J. M. (2011). Noctilio albiventris (Noctilionidae), a potential seed disperser in disturbed tropical dry forest habitats. Acta Chiropterologica, 13(1), 189- 194. https://doi.org/http://dx.doi.org/10.3161/150811011X578732 34. Arias, E., & Pacheco, V. (2019). Diet and trophic structure in an assemblage of bats in montane forest of Pampa Hermosa National Sanctuary, Junin, Peru. Revista Peruana de Biologia, 26(2). https://doi.org/10.15381/rpb.v26i2.16375 35. Arias-Cóyotl, E., Stoner, K. E., & Casas, A. (2006). 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Biotropica, 36(2), 131- 138. https://doi.org/Forest fragmentation and the resulting spatial isolation of tree species can modifj the activity of pollinators and may have important implications for the reproductive success and mating systems of the plants they pollinate. The objectives of this study were to (1) evaluate the effect of forest fragmentation on pollinator activity in bat-pollinated bombacaceous trees and (2) determine the effects of forest fragmentation on reproductive success and mating systems of bombacaceous trees. We studied these parameters in three bombacaceous tree species in tropical seasonal forest of Chamela, Jalisco, Mexico, and Osa and Guanacaste, Costa Rica. For Ceiba aesrulifolia, more visits were observed in fragments by both Glossopbaga soricina and Leptonycteris rurasoae. For Ceiba grandzfira, Musonyctmis barrijoni visited flowers exclusively in forest and G. soricina visited more flowers in forest than in fragments; no difference was shown by L. rurasoae. For Ceiba pentandra in Chamela, no differences were found in visitation by G. soricina between forest and fragments; L. curasoae visited significantly more flowers in forest. Ceiba pentandra received more visits by Pbyllostomus discolor than G. soricina in Guanacaste, whereas no bat visitors were observed in Osa. Total mean flower production was greater in fragments than forest for C. aesculifolia, whereas no difference was observed for C. grandzjora. Fruit set was greater in forest than in fragments for C. grandzfira, whereas no difference was observed for C. aesrulzfilia. Outcrossing rates were high for C. aesrulzjlia and C. grandzfira in Chamela, and for C. pentandra in Guanacaste, independent of tree habitat, while C. pentandra in Osa showed a mixed-mating system. The effects of forest fragmentation on bat pollinators, plant reproductive success, and mating patterns varied depending upon the bombacaceous species. 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