PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2012 | 14 | 1 |

Tytuł artykułu

Chemical composition of the substances from dorsal patches of males of the Curacaoan long-nosed bat, Leptonycteris curasoae (Phyllostomidae: Glossophaginae)

Warianty tytułu

Języki publikacji

EN

Abstrakty

In the absence of visual cues, chemical signals are especially important for nocturnal mammals such as bats, because they facilitate individual recognition, communication, and mate selection. In a recent study, it was reported that adult males of the Curaçaoan long-nosed bat, Leptonycteris curasoae, develop an odoriferous dorsal patch during the short mating season. It was postulated that dorsal patches signal health condition to females, and that females are preferentially attracted to the odor of males with dorsal patches. The chemical characterization of the dorsal patch is key to understanding its implications in chemical communication in a sexual context. In the present study, organic compounds collected from dorsal patches of males of L. curasoae from northwestern Venezuela were extracted using solid-phase micro-extraction (SPME) techniques and tentatively identified using GC-MS (Gas Chromatography-Mass Spectrometry). Nineteen compounds were present in 75% or more of the patches examined: 3-methyl-2-buten-1-thiol, acetic acid, 2′-aminoacetophenone, diacetyl, 2-pentanone, 2,3-dimethylpyrazine, 2-nonanone, acetamide, 2-undecanone, piperidinone, 4-methylquinazoline, 2,4-dimethylquinazoline, 3-methyl-2,5-pyrrolidinedione, 2-butanone, 2-methylfuran, 3-methyl-2-butenal, δ-valerolactone, 3-methyl-2-butenoic acid, and 2-methyl-2-butenoic acid. Although some of these compounds have been reported as important in female attraction among other male mammals during their respective breeding seasons, the actual function of these chemicals in L. curasoae remains to be determined. Some of these compounds have also been identified as natural insecticides, and this may be associated with lower ectoparasite loads reported on males with dorsal patches. These results, when considered along with previous observations, suggest that the dorsal patch in males of L. curasoae promotes the attraction of females during the mating season, and/or provides protection against ectoparasites.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

14

Numer

1

Opis fizyczny

p.213-224

Twórcy

  • Center for Ecology and Conservation Biology, Department of Biology, Boston University, Boston, MA 02215, USA
  • Microanalytics, 2011 A Lamar Drive, Round Rock, TX 78664, USA
autor
  • Centro de Ecologia, Institute Venezolane de Investigaciones Cientificas, Apartado 21827, Caracas 1020-A, Venezuela
autor
  • Center for Ecology and Conservation Biology, Department of Biology, Boston University, Boston, MA 02215, USA

Bibliografia

  • 1. J. D. Altringham , and M. B. Fenton . 2003. Sensory ecology and communication in the Chiroptera. Pp. 90–127, in Bat ecology ( T. H. Kunz and M. B. Fenton , eds.). Chicago University Press, Chicago, 779 pp. Google Scholar
  • 2. R. A. Alzogaray , A. Fontán , F. Camps , H. Masuh , P. Santo Orihuela , D. Fernandez , A. Cork , and E. Zerba . 2005. Behavioural response of Triatoma infestans (Klug) (Hemiptera: Reduviidae) to quinazolines. Molecules, 10: 1190–1196. Google Scholar
  • 3. K. F. Andersen , and T. Vulpius . 1999. Urinary volatile constituents of the lion, Panthera leo. Chemical Senses, 24: 179–189. Google Scholar
  • 4. R. J. E. Bailey , M. A. Birkett , A. Ingvarsdóttir , A. J. Mordue , W. Morue , B. O'Shea , J. A. Pickett , and L. J. Wadhams . 2006. The role of semiochemicals in host locations and non-host avoidance by salmon louse (Lepeophtheirus salmonis) copepodids. Canadian Journal of Fisheries and Aquatic Sciences, 63: 448–456. Google Scholar
  • 5. A. Blaustein 1981. Sexual selection and mammalian olfaction. American Naturalist, 117: 1006–1010. Google Scholar
  • 6. J. Bloss 1999. Olfaction and the use of chemical signals in bats. Acta Chiropterologica, 1: 31–45. Google Scholar
  • 7. J. Bloss , T. E. Acree , J. M. Bloss , W. R. Hood , T. H. Kunz . 2002. Potential use of chemical cues for colony-mate recognition in the big brown bat, Eptesicus fuscus. Journal of Chemical Ecology, 28: 819–834. Google Scholar
  • 8. S. Bouchard 2001. Sex discrimination and roostmate recognition by olfactory cues in the African bats, Mops condylurus and Chaerephon pumilus (Chiroptera: Molossidae). Journal of Zoology (London), 254: 109–117. Google Scholar
  • 9. P. A. Brennan , and K. M. Kendrick 2006. Mammalian social odours: attraction and individual recognition. Philosophical Transactions of the Royal Society, 361B: 2061–2078. Google Scholar
  • 10. A. P. Brooke , and D. M. Decker . 1996. Lipid compounds in secretions of fishing bat, Noctilio leporinus (Chiroptera: Noctilionidae). Journal of Chemical Ecology, 22: 1411–1428. Google Scholar
  • 11. A. K. Brunet-Rossini , and G. S. Wilkinson . 2009. Methods for estimating age in bats. Pp. 315–326, in Ecological and behavioral methods for the study of bats, 2nd edition ( T. H. Kunz and S. Parsons , eds.). The Johns Hopkins University Press, Baltimore, 901 pp. Google Scholar
  • 12. B. V. Burger , A. E. Nell , H. S. C. Spies , M. Le Roux , R. C. Bigalke , and P. A. J. Brand . 1999. Mammalian exocrine secretions. XII: Constituents of interdigital secretions of bontebok, Damaliscus dorcas dorcas, and blesbok, D. d. phillipsi. Journal of Chemical Ecology, 25: 2057–2084. Google Scholar
  • 13. B. A Caspers , F. C. Schroeder , S. Franke , J. W. Streich , and C. C. Voigt . 2009. Odour-based species recognition in two sympatric species of sac-winged bats (Saccopteryx bilineata, S. leptura): combining chemical analyses, behavioural observations and odour preference tests. Behavioral Ecology and Sociobiology, 63: 741–749. Google Scholar
  • 14. B.A. Caspers , F. Schroeder , S. Franke , and C. C. Voigt . 2011. The scent of adolescence: the maturation of the olfactory phenotype in a free ranging mammal. PLoS ONE, 6: 6. doi:10.1371/journal.pone.0021162 Google Scholar
  • 15. F. R. Cole , and D. E. Wilson . 2006. Leptonycteris curasoae. Mammalian Species, 796: 1–3. Google Scholar
  • 16. R. W. Dapson , E. H. Studier , M. J. Buckingham , and A. L. Studier . 1977. Histochemistry of odoriferous secretions from integumentary glands in three species of bats. Journal of Mammalogy, 58: 531–535. Google Scholar
  • 17. E. De Fanis , and G. Jones . 1995. The role of odour in discrimination of conspecifics by pipistrelle bats. Animal Behavior, 49: 835–839. Google Scholar
  • 18. J. A. Dean 1992. Lange's handbook of chemistry, 14 edition. McGraw-Hill, New York, 1466 pp. Google Scholar
  • 19. D. K. N. Dechmann , and K. Safi . 2005. Studying communication in bats. Cognitie, Creier, Comportament, 9: 479–496. Google Scholar
  • 20. R. L. Doty 1986. Odor-guided behavior in mammals. Experientia, 42: 257–271. Google Scholar
  • 21. K. D. Ehman , and M. E. Scott . 2002. Female mice mate preferentially with non-parasitized males. Parasitology, 125: 461–466. Google Scholar
  • 22. J. F. Eisenberg , and D. G. Kleiman . 1972. Olfactory communication in mammals. Annual Review of Ecology and Systematics, 3: 1–32. Google Scholar
  • 23. M. Fernández-Vargas , Z. Tang-Martínez , and S. M. Phelps . 2008. Olfactory responses of Neotropical short-tailed singing mice, Scotinomys teguina, to odors of the mid-ventral sebaceous gland: discrimination of conspecifics, gender, and female reproductive condition. Journal of Chemical Ecology, 34: 429–437. Google Scholar
  • 24. T. H. Fleming , and J. M. Nassar . 2002. Population biology of the lesser long-nosed bat Leptonycteris curasoae in Mexico and Northern South America. Pp. 283–305, in Columnar cacti and their mutualists: evolution, ecology, and conservation ( T. H. Fleming and A. Valiente-Banuet , eds.). University of Arizona Press, Tucson, 371 pp. Google Scholar
  • 25. W. L. Gannon , R. S. Sikes , and The Animal Care And Use Committee Of The American Society Of Mammalogists . 2007. Guidelines of the American Society of Mammalogists for the use of wild mammals in research. Journal of Mammalogy, 88: 809–823. Google Scholar
  • 26. Y. Q. Gu , M. H. Mo , J. P. Zhou , C. S. Zou , and K. Q. Zhang . 2007. Evaluation and identification of potential organic nematicidal volatiles from soil bacteria. Soil Biology and Biochemistry, 39: 2567–2575. Google Scholar
  • 27. M. K. Gustin , and G. F. McCracken . 1987. Scent recognition between females and pups in the bat Tadarida brasiliensis mexicana. Animal Behavior, 35: 13–19. Google Scholar
  • 28. V. P. Höller , and U. Schmidt . 1993. Olfactory communication in the lesser spear-nosed bat, Phyllostomus discolor (Chiroptera, Phyllostomidae). Zeitschrift für Säugetierkunde, 58: 257–265. Google Scholar
  • 29. C. S. Hood , and J. D. Smith . 1984. Histology of a sexually dimorphic integumentary gland in Macroglossus lacochilus (Chiroptera: Pteropodidae). Journal of Mammalogy, 65: 1–9. Google Scholar
  • 30. M. Kavaliers , and D. D. Colwell . 1993. Aversive responses of female mice to the odors of parasitized males: neuromodulatory mechanisms and implications for mate choice. Ethology, 95: 202–212. Google Scholar
  • 31. M. Kavaliers , and D. D. Colwell . 1995. Odours of parasitized males induce aversive responses in female mice. Animal Behavior, 50: 1161–1169. Google Scholar
  • 32. M. Kavaliers , M. A. Fudge , D. D. Colwell , and E. Choleris . 2003. Aversive and avoidance responses of female mice to the odors of males infected with an ectoparasite and the effects of prior familiarity. Behavioral Ecology and Sociobiology, 54: 423–430. Google Scholar
  • 33. P. H. Krutzsch 2000. Anatomy, physiology and cyclicity of the male reproductive tract. Pp. 91–155, m Reproductive biology of bats ( E. G. Crichton and P. H. Krutzsch , eds.). Academic Press, Cambridge, 510 pp. Google Scholar
  • 34. T. H. Kunz , C. Wemmer , and V. Hayssen . 1996. Sex, age and reproductive condition. Pp. 279–290, in Measuring and monitoring biological diversity. Standard methods for mammals ( D. E. Wilson , F. R. Cole , J. D. Nichols , R. Rudran , and M. S. Foster , eds.). Smithsonian Institution Press, Washington, D.C., 409 pp. Google Scholar
  • 35. T. H. Kunz , R. Hodgkison , and C. Weise . 2009. Methods of capturing and handling bats. Pp. 3–35, m Ecological and behavioral methods for the study of bats, 2nd edition ( T. H. Kunz and S. Parsons , eds.). The Johns Hopkins University Press, Baltimore, 901 pp. Google Scholar
  • 36. D. Lily , and J. Vanitharani . 2005. Chemical signaling in Hipposideros speoris. Journal of Theoretical and Experimental Biology, 1: 183–192. Google Scholar
  • 37. W. Lwande , A. Hassanali , P. G. McDowell , L. Moreka , S. K. Nokoe , and P. G. Waterman . 1992. Constituents of Commiphora rostrata and some of their analogs as maize weevil, Sitophilus zeamais repellents. Insect Science and its Application, 13: 679–683. Google Scholar
  • 38. A. Martino , A. Arends , and J. Aranguren . 1998. Reproductive pattern of Leptonycteris curasoae Miller (Chiroptera: Phyllostomidae) in northern Venezuela. Mammalia, 62: 69–76. Google Scholar
  • 39. M. Muñoz-Romo 2008. The dorsal patch and chemical signaling in the long-nosed bat, Leptonycteris curasoae in Venezuela. PhD Thesis, Boston University, Boston, 183 pp. Google Scholar
  • 40. M. MuÑOz-Romo , and T. H. Kunz . 2009. Dorsal patch and chemical signaling of males of the long-nosed bat, Leptonycteris curasoae (Chiroptera: Phyllostomidae). Journal of Mammalogy, 90: 1139–1147. Google Scholar
  • 41. M. Muñoz-Romo , J. F. Burgos , and T. H. Kunz . 2011a. Smearing behavior of males Leptonycteris curasoae (Chiroptera) and female response to the odor of male dorsal patches. Behaviour, 148: 461–483. Google Scholar
  • 42. M. Muñoz-Romo , J. F. Burgos , and T. H. Kunz . 2011b. The dorsal patch of males of the Curaçaoan long-nosed bat, Leptonycteris curasoae (Phyllostomidae: Glossophaginae) as a visual signal. Acta Chiropterologica, 13: 207–215. Google Scholar
  • 43. R. Mykytowycz , and B. S. Goodrich . 1974. Skin glands as organs of communication in mammals. Journal of Investigative Dermatology, 62: 124–131. Google Scholar
  • 44. J. M. Nassar , V. Salazar , A. Quintero , K. Stoner , A. Cabrera , M. Gómez , and K. Jaffé . 2008. Seasonal sebaceous patch in the nectar-feeding bats Leptonycteris curasoae and L. yerbabuenae (Phyllostomidae: Glossophaginae): Phenological, histological, and preliminary chemical characterization. Zoology, 111: 363–376. Google Scholar
  • 45. L. T. Nielsen , D. K. Eaton , D. W. Wright , and B. Schmidt-French . 2006. Characteristic odors of Tadarida brasiliensis mexicana Chiroptera: Molossidae. Journal of Cave and Karst Studies, 68: 27–31. Google Scholar
  • 46. J. Pawliszyn 1997. Solid phase microextraction: theory and practice. Wiley-VCH, New York, 247 pp. Google Scholar
  • 47. D. Penn , and W. K. Potts . 1998. Chemical signals and parasite-mediated sexual selection. Trends in Ecology and Evolution, 13: 391–396. Google Scholar
  • 48. P. A. Racey 2009. Reproductive assessment of bats. Pp. 247–264, in Ecological and behavioral methods for the study of bats, 2nd edition ( T. H. Kunz and S. Parsons , eds.). The Johns Hopkins Uuniversity Press, Baltimore, 901 pp. Google Scholar
  • 49. J. Ruther , S. Steiner , and L. A. Garbe . 2008. 4-Methylquinazoline is a minor component of the male sex pheromone in Nasonia vitripennis. Journal of Chemical Ecology, 34: 99–102. Google Scholar
  • 50. M. Ryg , Y. Solberg , C. Lydersen , and T. G. Smith . 1992. The scent of rutting male ringed seals (Phoca hispida). Journal of Zoology (London), 226: 681–689. Google Scholar
  • 51. K. Safi , and G. Kerth . 2003. Secretions of the interaural gland contain information about individuality and colony membership in the Bechstein's bat. Animal Behavior, 65: 363–369. Google Scholar
  • 52. S. Schulz , and J. S. Dickschat . 2007. Bacterial volatiles: the smell of small organisms. Natural Products Report, 24: 814–842. Google Scholar
  • 53. W. M. R Scully , M. B. Fenton , and A. S. M. Saleuddin . 2000. A histological examination of the holding sacs and glandular scent organs of some bat species (Emballonuridae, Hipposideridae, Phyllostomidae, and Molossidae). Canadian Journal of Zoology, 78: 613–623. Google Scholar
  • 54. E. H. Studier , and K. H. Lavoie . 1984. Microbial involvement in scent production in noctilionid bats. Journal of Mammalogy, 65: 711–714. Google Scholar
  • 55. J. Vanitharani , M. Vijaya , and D. Lily . 2007. Scent gland and chemical signaling in Cynopterus sphinx (short-nosed fruit bat) during breeding season. Journal of Theoretical and Experimental Biology, 3: 67–75. Google Scholar
  • 56. G. Vas , And K. Vékey . 2004. Solid-phase microextraction: a powerful sample preparation tool prior to mass spectrometric analysis. Journal of Mass Spectrometry, 39: 233–254. Google Scholar
  • 57. C. C. Voigt 2002. Individual variation in perfume blending in male greater sac-winged bats. Animal Behavior, 63: 907–913. Google Scholar
  • 58. C. C. Voigt , and O. Von Helversen . 1999. Storage and display of odour by male Saccopteryx bilineata (Chiroptera, Emballonuridae). Behavioral Ecology and Sociobiology, 47: 29–40. Google Scholar
  • 59. C. C. Voigt , O. Von Helversen , R. Michener , and T. H. Kunz . 2001. The economics of harem maintenance in the sacwinged bat, Saccopteryx bilineata (Emballonuridae). Behavioral Ecology and Sociobiology, 50: 31–36. Google Scholar
  • 60. C. C. Voigt , B. Caspers , and S. Speck 2005. Bats, bacteria, and bat smell: sex-specific diversity of microbes in a sexually selected scent organ. Journal of Mammalogy, 86: 745–749. Google Scholar
  • 61. C. C. Voigt , G. Heckel , and O. Von Helversen . 2006. Conflicts and strategies in the harem-polygynous mating system of the sac-winged bat, Saccopteryx bilineata. Pp. 269–289, in Functional and evolutionary ecology of bats ( A. Zubaid , G. F. Mccracken , and T. H. Kunz , eds.). Oxford University Press, New York, 342 pp. Google Scholar
  • 62. W. F. Wood , and J. M. Szewczak . 2007. Volatile antimicrobial compounds in the pelage of the Mexican free-tailed bat, Tadarida brasiliensis. Biochemical Systematics and Ecology, 35: 566–568. Google Scholar
  • 63. W. F. Wood , A. Walsh , J. Seyjagat , and P. J. Weldon . 2005. Volatile compounds in shoulder gland secretions of male flying foxes, genus Pteropus (Pteropodidae, Chiroptera). Zeitschrift für Naturforschung, 60: 779–784. Google Scholar
  • 64. D. W. Wright , D. E. Eaton , L. T. Nielsen , F. W. Kuhrt , J. A. Koziel , J. P. Spinhirne , and F. B. Parker . 2005. Multidimensional gas chromatography-olfactometry for the identification and prioritization of malodors from confined animal feeding operations. Journal of Agricultural and Food Chemistry, 53: 8663–8672. Google Scholar
  • 65. J. X. Zhang , H. A. Soini , K. E. Bruce , D. Wiesler , S. K. Woodley , M. J. Baum , and M. V. Novotny . 2005. Putative chemosignals of the ferret (Mustela furo) associated with individual and gender recognition. Chemical Senses, 30: 727–737. Google Scholar

Uwagi

PL
Rekord w opracowaniu

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-4d1bb66f-6c02-406b-94b9-81e7ea3955ba
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.