Molt Associated Hematocrit Changes in African Penguins, Spheniscus demersus
IAAAM Archive
Delphine Sarran; J. Lawrence Dunn; Lisa Mazzaro
Research and Veterinary Services, Mystic Aquarium
Mystic, CT, USA

Abstract

An assay of hematologic parameters is an important component of a complete health examination, and has obvious value in the assessment of patients or the reassessment of post-treatment patients. In Sphenisciforms published reference ranges for hematocrit and erythrocyte counts are not well documented. Several years of blood sampling from the African Black Footed penguins (Spheniscus demersus) at Mystic Aquarium and interpretation of their hemograms have documented seasonal hematologic variations. Hematocrit especially has been noted to decline without evidence of injury or disease and to increase subsequently in the absence of any treatment. Previous studies conducted on various avian species examined the effects of age, sex, time of day, breeding and physiologic status on several blood parameters but hematocrit variation has received little attention in hematological studies of penguins.2,5,6,8,9,15,16,25,27

This study was designed to examine hematocrit variations in relation to the physiological status of the African Black Footed penguins and, specifically, to determine how molt influences that parameter. We hypothesize that molt imposes hormonal, immunological and energetic challenges that result in a hematocrit decrease in otherwise healthy birds.1,18 239 samples were collected from healthy birds in the period 1995-2005. Most (222) were routinely scheduled samplings and only 17 were collected during the molt. All birds were sampled from the jugular vein, usually in early morning. Hematocrit was determined as the percentage of packed red cell volume to total column height (plasma + packed red cell volume). All hematocrit measurements were made within 3 hours of sampling. One Way Analysis of Variance (ANOVA) was used for comparison of the hematocrit in molting versus non molting birds. Although the sample size in this study was limited, the results showed a statistically significant difference (p<0.05) in hematocrit between molting and non molting birds. The hematocrit of molting birds averaged approximately 7.4% less than the hematocrit of non molting birds, thus supporting our hypothesis.

A number of hypotheses have been advanced to explain this reduction in hematocrit during the molt. Since hematocrit is only a measurement of relative volume, it can vary because of changes in the size and/or numbers of hemocytes or in plasma volume. Hematocrit may decline because of (1) a reduction in erythropoiesis secondary to nutritional and energetic imbalances undergone during the molt including some degree of fasting, potentially leading to iron deprivation.1,11,23,29 Previous studies on Humboldt penguins (Spheniscus humboldti) show that molting is associated with low concentrations of sex steroid hormones and a drastic increase and subsequent decrease of thyroid hormones. These hormonal changes may influence hematological values.3,4,7,10,12,13,14,17,19,20,21,22,24,26,28

A second (2) possible explanation for the decrease in hematocrit is hemodilution, an increase in plasma volume as an osmotic adjustment in response to the extensive vascularization of growing feathers without an accompanying increase in erythrocyte population or size.6,29,30

These hypotheses are not mutually exclusive and therefore a combination of patterns may be observed. Results of this pilot study have confirmed for us the need to initiate a more complex investigation to determine the cause(s) of the molt associated hematocrit decline.

References

1.  Bougaeff S, Dorst J. 1975. Weight variations and energy expenditure in the Adelie penguin (Pygoscelis adeliae). C R Acad Sci Hebd Seances Acad Sci D 280 (20): 2373-6.

2.  Brake J, Baker M, Morgan GW, Thaxton P. 1982. Physiological changes in caged layers during a forced molt. 4. Leukocytes and packed cell volume. Poult Sci Apr 61(4):790-5.

3.  Cherel Y, Robin JP, Walch O, Karmann H, Netchitailo P, Le Maho Y. 1988. Fasting inking penguin. I. Hormonal and metabolic changes during breeding. Am. J. Physiol. Regul Integr Comp Physiol 254:170-177.

4.  Cherel Y, Leloup J, Le Maho Y. 1988. Fasting in king penguin. II. Hormonal and metabolic changes during molt. Am J Physiol Regul Integr Comp Physiol 254:178-184.

5.  Dawson R, Bortolotti G. 1997. Variation in hematocrit and total plasma proteins of nestling American kestrels (Falco sparverius) in the wild. Comp. Biochem.Physiol.117 (A):383-390.

6.  De Graw WA, Kern MD. 1985. Changes in the blood and plasma volume of Harris' sparrows during postnuptial molt. Comp. Biochem.Physiol.81 (4):889-93.

7.  Dickerman RW, Bahr JM. 1989. Molt induced by gonadotropin-releasing hormoneagonist as a model for studying endocrine mechanisms of molting in laying hens. Poult.Sci.68(10):1402-8.

8.  Driver EA. 1981. Hematological and blood chemical values of mallard, Anas platyrhynchos, drakes before, during and after remige moult. J. Wildl. Dis. 17: 413-421.

9.  Gayathri KL, Hedge SN. 2005. Alteration in haematocrit values and plasma protein fractions during the breeding cycle of female pigeons, Columba livia. Animal Reproduction Science 2728, 9 pages.

10. Groscolas R, Leloup J. 1986. The endocrine control of reproduction and molt in male and female emperor (Aptenodytes forsteri) and adelie (Pygoscelis adeliae) penguins. II. Annual changes in plasma levels of thyroxine and triiodothyronine. Gen Comp Endocrinol 63(2):264-274.

11. Groscolas R, Robin JP. 2001. Long-term fasting and re-feeding in penguins. Comparative Biochemistry and Physiology Part A 128:645-655.

12. Herremans M, Decuypere E, Chiasson RB. Role of ovarian steroids in the control of moult induction in laying fowls. 1988. Br Poult.Sci. 29(1): 125-36.

13. Kuenzel WJ. 2003. Neurobiology of molt in avian species. Poult. Sci. Jun 82(6): 981-91.

14. Le Ninan F, Cherel Y, Robin JP, Leloup J, Le Maho Y. 1988. Early changes in plasma hormones and metabolites during fasting in king penguin chicks. J Comp Physiol B 158:395-401.

15. Merino S, Barbosa A. 1997. Haematocrit values in chinstrap penguins (Pygoscelisantarctica): variation with age and reproductive status. Polar Biol 17:14-16.

16. Morton LM. 1993. Hematocrits in montane sparrows in relation to reproductive schedule. The Condor 96:119-126.

17. Otsuka R, Machida T, Wada M. 2004. Hormonal correlations at transition from reproduction to molting in an annual life cycle of Humboldt penguins (Spheniscushumboldti). Gen.Comp.Endocrinol. 135: 175-85.

18. Penney RL. 1967. Molt in the adelie penguin. The Auk, 84:61-71.

19. Queen WH, Christensen VL, May JD. 1997. Supplemental thyroid hormones and molting in turkey breeder hens. Poult.Sci. 76:887-893.

20. Reidarson TH, McBain JF, Denton D. 1999. The use of medroxyprogesterone acetate to induce molting in chinstrap penguins (Pygoscelis antartica). J Zoo Wildl Med Jun 30(2):278-80.

21. Reinert BD, Wilson FE. 1997. Effects of Thyroxine and Triiodothyronine replacement therapy on the programming of seasonal reproduction and postnuptial molt in thyroidectomized male American tree sparrows (Spizella arborea) exposed to long days. J.Exp.Zool. 279:367-376.

22. Remage-Healey L, Romero LM. 2002. Corticosterone and insulin interact to regulateplasma glucose but not lipid concentrations in molting starlings. Gen.Comp.Endrinol. 129:88-94.

23. Robin JP, Frain M, Sardet C, Groscolas R, Le Maho Y. 1988. Protein and lipid utilization during long-term fasting in emperor penguins. Am J Physiol 254(1 Pt 2):R61-8.

24. Romero LM, Strochlic D, Wingfield JC. 2005. Corticosterone inhibits feather growth: potential mechanism explaining seasonal down regulation of corticosterone during molt. Comp.Biochem.Physiol. (A) 142:65-73.

25. Sergent N, Rogers T, Cunningham M. 2004. Influence of biological and ecological factors on hematological values in wild Littele Penguins, Eudyptula minor. Comp. Biochem.Physiol 138:333-339.

26. Smith JP. 1982. Changes in blood levels of thyroid hormones on two species of passerine birds. The Condor 84:160-167.

27. Svensson E, Merila J. 1996. Molt and migratory condition in blue tits: a serological study. The Condor 98:825-831.

28. Szelenyi Z, Peezely P. 1988. Thyroxine induced moult in domestic hen. Acta Physiol Hung 72(2):143-9.

29. Watson GE. 1963. The mechanism of feather replacement during natural molt. The Auk 80:486-495.

30. Williams TD, Challenger WO, Christians JK, Evanson M, Love O, Vezina F.2004.What causes the decrease in haematocrit during egg production? Functional Ecology 18:330-336.

Speaker Information
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Delphine Sarran


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