Register      Login
Emu Emu Society
Journal of BirdLife Australia
RESEARCH ARTICLE

First report of a feather loss condition in Adelie penguins (Pygoscelis adeliae) on Ross Island, Antarctica, and a preliminary investigation of its cause

Wray W. Grimaldi A E , Richard J. Hall B , Daniel D. White C , Jing Wang B , Melanie Massaro D and Daniel M. Tompkins C
+ Author Affiliations
- Author Affiliations

A Department of Zoology, University of Otago, Department of Zoology, PO Box 56, Dunedin 9054, New Zealand.

B Institute of Environmental Science and Research, 66 Ward St, Upper Hutt 5018, New Zealand.

C Landcare Research, Private Bag 92170, Auckland Mail Centre, Auckland 1142, New Zealand.

D School of Environmental Sciences, Charles Sturt University, PO Box 789, Albury NSW 2640, Australia.

E Corresponding author. Email: wray.grimaldi@postgrad.otago.ac.nz

Emu 115(2) 185-189 https://doi.org/10.1071/MU14068
Submitted: 14 July 2014  Accepted: 18 December 2014   Published: 30 April 2015

Abstract

Since the mid-1980s, observations of marine animals with alopecia have been reported worldwide, although in most cases specific causes and consequences have not been elucidated. Adding to that list, an unprecedented feather loss condition affecting ~1 in 1000 adult Adelie penguins was observed at the beginning of December 2011 at each of three colonies on Ross Island, Antarctica. Feather loss was again observed in 2012–13 and 2013–14. The condition was characterised by irregular patches of bare skin on various parts of the body well before the usual period of moult. Blood samples, plucked feathers and cloacal swabs were obtained to investigate the cause or causes of this abnormal loss of feathers. No ectoparasites were detected on physical inspection of any birds or by scanning electron microscopy of feathers removed from birds experiencing feather loss. Blood smears were negative for hemoparasites. There was statistical support for mild lymphocytosis and moderate basophilia from the results of white blood-cell differentials in penguins with feather loss compared with those with no feather loss. Blood samples were negative to a PCR diagnostic specific for beak and feather disease virus. Three new putative RNA viruses were detected by high-throughput sequencing of cloacal samples, showing similarity to rotaviruses, astroviruses and picornaviruses. Although the significance of these viruses is not known, extended investigation into this feather loss condition is needed.

Additional keywords: alopecia, astrovirus, blood differentials, electron microscopy, metagenomic, pathogen discovery, virus.


References

Ainley, D. G. (2002). The Ross Sea, Antarctica, where all ecosystem processes still remain for study, but maybe not for long. Marine Ornithology 30, 55–62.

Barbosa, A., Colominas-Ciuró, R., Coria, N., Centurión, M., Sandler, R., Negri, A., and Santos, M. (2015). First record of feather-loss disorder in Antarctic penguins. Antarctic Science 27, 69–70.

Borriello, F., Granata, F., and Marone, G. (2014). Basophils and skin disorders. Journal of Investigative Dermatology 134, 1202–1210.
Basophils and skin disorders.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhsl2jtLw%3D&md5=606b7b84a27b18c5de3e80aa79a7a3fbCAS | 24499736PubMed |

Brush, A. (1996). On the origin of feathers. Journal of Evolutionary Biology 9, 131–142.
On the origin of feathers.Crossref | GoogleScholarGoogle Scholar |

Campbell, T. W., and Ellis, C. K. (2007). Hematology of birds. In ‘Avian and Exotic Animal Hematology and Cytology’. pp. 3–50. (Blackwell Publishing: Ames, IA.)

Cromheecke, J. L., Nguyen, K. T., and Huston, D. P. (2014). Emerging role of human basophil biology in health and disease. Current Allergy and Asthma Reports 14, 408.
Emerging role of human basophil biology in health and disease.Crossref | GoogleScholarGoogle Scholar | 24346805PubMed |

Davis, A. K., Maney, D. L., and Maerz, J. C. (2008). The use of leukocyte profiles to measure stress in vertebrates: a review for ecologists. Functional Ecology 22, 760–772.
The use of leukocyte profiles to measure stress in vertebrates: a review for ecologists.Crossref | GoogleScholarGoogle Scholar |

de Benedictis, P., Schultz-Cherry, S., Burnham, A., and Cattoli, G. (2011). Astrovirus infections in humans and animals – molecular biology, genetic diversity, and interspecies transmissions. Infection, Genetics and Evolution 11, 1529–1544.
Astrovirus infections in humans and animals – molecular biology, genetic diversity, and interspecies transmissions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXht1yltr7I&md5=a5d652f45ac881adc987db399d3a7f6bCAS | 21843659PubMed |

Decuypere, E., and Verheye, G. (1986). Physiological basis of induced moulting and tissue regeneration in fowls. World’s Poultry Science Journal 42, 56–68.
Physiological basis of induced moulting and tissue regeneration in fowls.Crossref | GoogleScholarGoogle Scholar |

Estes, M. K., Palmer, E. L., and Obijeski, J. F. (1983). Rotaviruses: a review. Current Topics in Microbiology and Immunology 105, 123–184.
Rotaviruses: a review.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2cXjtFSk&md5=c61c3aab7c480bc0c8d2b65083d9d1dcCAS | 6313296PubMed |

Gauthier-Clerc, M., Clerquin, Y., and Handrich, Y. (1998). Hyperinfestation by ticks Ixodes uriae: a possible cause of death in adult King Penguins, a long-lived seabird. Colonial Waterbirds 21, 229–233.
Hyperinfestation by ticks Ixodes uriae: a possible cause of death in adult King Penguins, a long-lived seabird.Crossref | GoogleScholarGoogle Scholar |

Harvey, J. W. (2012). Evaluation of leukocytic disorders. In ‘Veterinary Hematology: A Diagnostic Guide and Color Atlas’. pp. 122–176. (Elsevier: St. Louis, MO.)

Hawkey, C. M., Dennett, T. B., and Pierce, M. A. (1989). Normal and abnormal granulocytes. In ‘A Colour Atlas of Comparative Veterinary Haematology’. pp. 58–106. (Wolfe Medical Publications Ltd: London.)

Hays, H., and Risebrough, R. W. (1972). Pollutant concentrations in abnormal young terns from Long Island Sound. Auk 89, 19–35.
Pollutant concentrations in abnormal young terns from Long Island Sound.Crossref | GoogleScholarGoogle Scholar |

Honkavuori, K. S., Shivaprasad, H. L., Briese, T., Street, C., Hirschberg, D. L., Hutchison, S. K., and Lipkin, W. I. (2011). Novel picornavirus in Turkey poults with hepatitis, California, USA. Emerging Infectious Diseases 17, 480–487.
Novel picornavirus in Turkey poults with hepatitis, California, USA.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXktlehu7o%3D&md5=f4c7da67f570b1ca086c7e844e02dbe6CAS | 21392440PubMed |

Kane, O. J., Smith, J. R., Boersma, P. D., Parsons, N. J., Strauss, V., Garcia-Borboroglu, P., and Villanueva, C. (2010). Feather-loss disorder in African and Magellanic Penguins. Waterbirds 33, 415–421.
Feather-loss disorder in African and Magellanic Penguins.Crossref | GoogleScholarGoogle Scholar |

Le Bohec, C., Whittington, J. D., and Le Maho, Y. (2011). Polar monitoring: seabirds as sentinels of marine ecosystems. In ‘Adaptation and Evolution in Marine Environments. Vol. 2: From Pole to Pole’. (Eds C. Verde and G. di Prisco.) pp. 205–230. (Springer-Verlag: Berlin Heidelberg.)

Lebigre, C., Alatalo, R., Kilpimaa, J., Staszewski, V., and Siitari, H. (2012). Leucocyte counts variation and measures of male fitness in the lekking Black Grouse. Journal für Ornithologie 153, 95–102.
Leucocyte counts variation and measures of male fitness in the lekking Black Grouse.Crossref | GoogleScholarGoogle Scholar |

Leeson, S., and Walsh, T. (2004). Feathering in commercial poultry. II. Factors influencing feather growth and feather loss. World’s Poultry Science Journal 60, 52–63.
Feathering in commercial poultry. II. Factors influencing feather growth and feather loss.Crossref | GoogleScholarGoogle Scholar |

McFarlane, R. (1996). Some observations on Adelie penguin (Pygoscelis adeliae) mortality in East Antarctica. Avian Pathology 25, 187–190.
Some observations on Adelie penguin (Pygoscelis adeliae) mortality in East Antarctica.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD1cvmslCitA%3D%3D&md5=41fba4c38c4c5fd720755d10dd424468CAS | 18645851PubMed |

Møller, A. P., Nielsen, J. T., and Erritzøe, J. (2006). Losing the last feather: feather loss as an antipredator adaptation in birds. Behavioral Ecology 17, 1046–1056.
Losing the last feather: feather loss as an antipredator adaptation in birds.Crossref | GoogleScholarGoogle Scholar |

Pantin-Jackwood, M. J., Spackman, E., and Woolcock, P. R. (2006). Molecular characterization and typing of Chicken and Turkey astroviruses circulating in the United States: implications for diagnosis. Avian Diseases 50, 397–404.
Molecular characterization and typing of Chicken and Turkey astroviruses circulating in the United States: implications for diagnosis.Crossref | GoogleScholarGoogle Scholar | 17039840PubMed |

Penney, R. L. (1967). Molt in the Adelie Penguin. Auk 84, 61–71.
Molt in the Adelie Penguin.Crossref | GoogleScholarGoogle Scholar |

Prum, R. (1999). Development and evolutionary origin of feathers. Journal of Experimental Zoology 285, 291–306.
Development and evolutionary origin of feathers.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3c%2FkslWjtg%3D%3D&md5=52521a0662411d08df68d530472bdf0bCAS | 10578107PubMed |

Quesada, Ó., Rodríguez, F., Herráez, P., Seara, D., and Espinosa de los Monteros, A. (2007). Mucor ramosissimus associated with feather loss in Canaries (Serinus canarius). Avian Diseases 51, 643–645.
Mucor ramosissimus associated with feather loss in Canaries (Serinus canarius).Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2svgvVKksQ%3D%3D&md5=d7f8768cae4a9f903e3da508bf45f394CAS | 17626501PubMed |

Savory, C. J. (1995). Feather pecking and cannibalism. World’s Poultry Science Journal 51, 215–219.
Feather pecking and cannibalism.Crossref | GoogleScholarGoogle Scholar |

Schmidt, R. E. (2002). Avian thyroid metabolism and diseases. Seminars in Avian and Exotic Pet Medicine 11, 80–83.
Avian thyroid metabolism and diseases.Crossref | GoogleScholarGoogle Scholar |

Schmidt, R. E., and Lightfoot, T. L. (2003). Integument. In ‘Clinical Avian Medicine’. (Eds G. J. Harrison and T. L. Lightfoot.) pp. 395–410. (Spix Publishing: Palm Beach, FL.)

Seddon, P., and Van Heezik, Y. (1991). Effects of hatching order, sibling asymmetries, and nest site on survival analysis of Jackass Penguin chicks. Auk 108, 548–555.
Effects of hatching order, sibling asymmetries, and nest site on survival analysis of Jackass Penguin chicks.Crossref | GoogleScholarGoogle Scholar |

Spearman, R. I. C., and Hardy, J. A. (1985). Integument. In ‘Form and Function in Birds. Vol. 3’. (Eds A. S. King and J. McLelland.) pp. 1–52. (Academic Press: London.)

Trojnar, E., Otto, P., Roth, B., Reetz, J., and Johne, R. (2010). The genome segments of a Group D rotavirus possess Group A-like conserved termini but encode group-specific proteins. Journal of Virology 84, 10254–10265.
The genome segments of a Group D rotavirus possess Group A-like conserved termini but encode group-specific proteins.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtlars7%2FP&md5=cddfa08e813c954716f5457cab55d9caCAS | 20631147PubMed |

Voehringer, D. (2011). Basophils in allergic immune responses. Current Opinion in Immunology 23, 789–793.
Basophils in allergic immune responses.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhsFOhtLnP&md5=3e0c541f7e953f5eca50912a1a259d56CAS | 22035810PubMed |