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Australian Journal of Zoology Australian Journal of Zoology Society
Evolutionary, molecular and comparative zoology
RESEARCH ARTICLE

A multiyear comparison of the male reproductive biology of the brown treesnake (Boiga irregularis) from Guam and the native range

Robert D. Aldridge A C , Dustin S. Siegel A , Angelo P. Bufalino A , Samantha S. Wisniewski A B and Benjamin C. Jellen A
+ Author Affiliations
- Author Affiliations

A Department of Biology, Saint Louis University, 3507 Laclede Avenue, St Louis, MO 63103-2010, USA.

B Caesar Kleberg Wildlife Research Institute, Texas A&M University, Kingsville, TX 78363-8202, USA.

C Corresponding author. Email: aldridge@slu.edu

Australian Journal of Zoology 58(1) 24-32 https://doi.org/10.1071/ZO09068
Submitted: 13 June 2009  Accepted: 3 February 2010   Published: 7 April 2010

Abstract

Previous studies have suggested that reproduction in the brown treesnake (Boiga irregularis) is reduced on Guam because of elevated stress hormones caused by limited food availability. This study examined the reproductive anatomy of male brown treesnakes on Guam over a 15-year period (1985–99) to determine whether the size at maturity and development of the testis and sexual segment of the kidney varied between years and to compare these data to those for snakes collected from the native range. On Guam, the average snout–vent length and body mass of B. irregularis has decreased from its high in 1985 and remained stable from 1989 to 1999. The snout–vent length at maturity was similar between years. Mean diameters of the seminiferous tubule and the sexual segment of the kidney were not significantly different between years. However, the number of sexual segment tubules hypertrophied per snake varied greatly. Snakes from the native range matured at smaller snout–vent lengths and had significantly more hypertrophied sexual segment tubules per kidney than populations on Guam. These data suggest that elevated plasma levels of corticosterone, potentially due to an increase in male–male interactions as a result the explosive population growth experienced on Guam, may be negatively influencing male reproduction.

Additional keywords: spermatogenesis, sexual segment of the kidney.


Acknowledgements

This project was funded by the National Biological Service to RDA. Animal Care Protocol 744 was approved through the Saint Louis University Animal Care Committee. We thank Mark Doles, Stan Kot, Gordon Rodda, Thomas Sharp, and Gad Perry for field and laboratory assistance on Guam, and Jennifer Pawlik, Tim Schmalz and Anna Arackal for laboratory assistance at Saint Louis University. We also thank George R. Zug, National Museum of Natural History, Smithsonian Institution; Howard L. Snell, Museum of South-Western Biology, University of New Mexico; and Alan E. Leviton, California Academy of Science, for permission to examine museum specimens.


References

Aldridge, R. D. , and Arackal, A. A. (2005). Reproductive biology and stress of captivity in male brown treesnakes (Boiga irregularis) on Guam. Australian Journal of Zoology 53, 249–256.
Crossref | GoogleScholarGoogle Scholar | Aldridge R. D. , Jellen B. C. , Siegel D. S. , and Wisniewski S. S. (In press). The sexual segment of the kidney. In ‘Reproductive Biology and Phylogeny of the Ophidia. Volume 4’. (Eds R. D. Aldridge and D. M. Sever.) (Science Publishers, Inc.: Enfield, NH.)

Bishop, J. E. (1959). A histological and histochemical study of the kidney tubule of the common garter snake, Thamnophis sirtalis, with special reference to the sexual segment in the male. Journal of Morphology 104, 307–357.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Ehmann H. (1992). ‘Encyclopedia of Australian Reptiles.’ (Collins, Angus and Robertson: Sydney.)

Krohmer, R. W. , Grassman, M. , and Crews, D. (1987). Annual reproductive cycle in the male red-sided garter snake, Thamnophis sirtalis parietalis: field and laboratory studies. General and Comparative Endocrinology 68, 64–75.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Rodda G. H. , McCoid M. J. , Fritts T. H. , and Campbell E. W. III (1999). Population trends and limiting factors in Boiga irregularis. In ‘Problem Snake Management: The Habu and Brown Treesnake’. (Eds G. H. Rodda, U. Sawai, D. Chizar and H. Tanaka.) pp. 236–253. (Cornell University Press: Ithaca, NY.)

Rodda, G. H. , Dean-Bradley, K. , Savidge, J. A. , Christy, M. T. , and Tyrrell, C. L. (2008). Post-colonization reversal of selection pressure on dispersal behavior of the brown treesnake, Boiga irregularis, on Guam. South American Journal of Herpetology 3, 123–134.
Crossref | GoogleScholarGoogle Scholar |

Savidge, J. A. (1987). Extinction of an island forest avifauna by an introduced snake. Ecology 68, 660–668.
Crossref | GoogleScholarGoogle Scholar |

Savidge, J. A. , Qualls, F. J. , and Rodda, G. H. (2007). Reproductive biology of the brown tree snake, Boiga irregularis (Reptilia: Colubridae), during colonization of Guam and comparison with that in their native range. Pacific Science 61, 191–199.
Crossref | GoogleScholarGoogle Scholar |

Schuett, G. W. , and Grober, M. S. (2000). Post-fight levels of plasma lactate and corticosterone in male copperheads, Agkistrodon contortrix (Serpentes, Viperidae): differences between winners and losers. Physiology & Behavior 71, 335–341.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Schuett, G. W. , Harlow, H. J. , Rose, J. D. , Van Kirk, E. A. , and Murdoch, W. J. (1996). Levels of plasma corticosterone and testosterone in male copperheads (Agkistrodon contortrix) following staged fights. Hormones and Behavior 30, 60–68.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Schuett, G. W. , Harlow, H. J. , Rose, J. D. , Van Kirk, E. A. , and Murdoch, W. J. (1997). Annual cycle of plasma testosterone in male copperheads, Agkistrodon contortrix (Serpentes, Viperidae): relationship to timing of spermatogenesis, mating, and agonistic behavior. General and Comparative Endocrinology 105, 417–424.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Shine, R. (1991). Strangers in a strange land: ecology of the Australian colubrid snakes. Copeia 1991, 120–131.
Crossref | GoogleScholarGoogle Scholar |

Siegel, D. S. , Aldridge, R. D. , Clark, C. S. , Poldemann, E. H. , and Gribbins, K. M. (2009). Stress and reproduction in Boiga irregularis with notes on the ultrastructure of the sexual segment of the kidney in squamates. Canadian Journal of Zoology 87, 1138–1146.
Crossref | GoogleScholarGoogle Scholar |

Taylor, E. N. , DeNardo, D. F. , and Jennings, D. H. (2004). Seasonal steroid hormone levels and their relation to reproduction in the western diamond-backed rattlesnake, Crotalus atrox (Serpentes: Viperidae). General and Comparative Endocrinology 136, 328–337.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Waye, H. L. , and Mason, R. T. (2008). A combination of body condition measurements is more informative than conventional condition indices: temporal variation in body condition and corticosterone in brown tree snakes (Boiga irregularis). General and Comparative Endocrinology 155, 607–612.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Weil, M. R. (1985). Comparison of plasma and testicular testosterone levels during the active season in the common garter snake, Thamnophis sirtalis (L.). Comparative Biochemistry and Physiology 81A, 585–587.
CAS |

Weil, M. R. , and Aldridge, R. D. (1981). Seasonal androgenesis in the male water snake, Nerodia sipedon. General and Comparative Endocrinology 44, 44–53.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Whittier, J. M. , and Limpus, D. (1996). Reproductive patterns of a biologically invasive species: the brown tree snake (Boiga irregularis) in eastern Australia. Journal of Zoology (London, England) 238, 591–597.
Crossref | GoogleScholarGoogle Scholar |

Zaidan, F. , Kreider, D. L. , and Beaupre, S. J. (2003). Testosterone cycles and reproductive energetics: implications for northern range limits of the cottonmouth. Copeia 2003, 231–240.
Crossref | GoogleScholarGoogle Scholar |




Appendix 1

Snakes examined from: Museum of Southwestern Biology MSB# 44012, 44025, 44027, 44031, 44035, 44040, 44042, 44047, 44054, 44094, 44097, 44098, 44099, 44134, 44227, 44237, 44241 (Guam); Smithsonian Institution USNM# 120067, 120068, 120070, 120236 (Cape Torokina, Bougainville Island); 195594 (Boroko, Papua New Guinea), 215939 (Indonesia); 506837, 506848, 506859, 506863, 506873, 506888, 506889, 506892, 506893, 507670, 507675, 507717 (Guam); California Academy of Sciences CAS# 114104 (Wahgi-Chimbu Junction, New Guinea), 121223 (Lake Murray, Maka, New Guinea), 133801 (Karemgok, New Guinea), 135568 (Daru Island, New Guinea), 135570 (Maka, Lake Murray, New Guinea).