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Morphometric Parameters of Erythrocytes in Juvenile Mandarin Ducks Aix galericulata

ABSTRACT

The morphometric parameters of erythrocytes in Mandarin ducks- Aix galericulata have never been subjected to study even though this species is common in aviculture. The aim of this study is to investigate the morphometric parameters of erythrocytes in juvenile Mandarin ducks. A total of 1500 erythrocytes obtained from thirty Mandarin ducks were analysed. The smears of the peripheral blood were stained using Diff-Quik® stain method, and the length and width of erythrocytes were measured using ImageJ program. The average length of the measured erythrocytes was 11.879 µm. The maximal measured length of the erythrocytes was 16.049 µm, and the minimal measured length was 5.668 µm. The average width of the measured erythrocytes was 6.160 µm. The maximal measured width of the erythrocytes was 10.115 µm and the minimal measured width was 3.750 µm. In conclusion, knowing morphometric parameters of Mandarin duck erythrocytes is the first step in evaluation process of erythrocytes’ functional state and health condition of an individual.

Keywords:
Blood smears; erythrocytes; mandarin duck; morphometric parameters

INTRODUCTION

Several studies have described morphometric parameters and hematological characteristics of non-domestic Anseriformes, including: three species of geese (Williams & Trainer, 1971Williams JI, Trainer DO.A hematological study of snow, blue, and Canada geese. Journal of Wildlife Diseases 1971;7:258-265.), canvasback duck Aythyavalisineria (Kocan & Pitts, 1976Kocan RM, Pitts SM. Blood values of the canvasback duck by age, sex and season, Journal of Wildlife Diseases 1976;12:341-345.), Pacific black duck Anas superciliosa (Mulley, 1979Mulley RC. Haematology and blood chemistry of the black duck (Anas supercilliosa). Journal of Wildlife Diseases 1979;15:473-441.), Australian wood duck Chenonettajubata (Mulley, 1980) and mallard Anas platyrhynchos (Driver, 1981Driver EA. Hematological and blood chemical values of mallard, Anas platyrhynchos, drakes before, during and after remigemoult. Journal of Wildlife Diseases 1981;17:413-421.; Fairbrother et al., 1990Fairbrother A, Craig MA, Walker K, O'Loughlin D. Changes in mallard (Anas platyrhynchos) serum chemistry due to age, sex, and reproductive condition. Journal of Wildlife Diseases 1990;26:67-77.; Fairbrother & O’Loughlin, 1990; Levengoodet al., 2000Levengood JM, Sanderson GC, Anderson WL, Foley GL, Brown PW, Seets JW. Influence of diet on the hematology and serum biochemistry of zinc-intoxicated mallards. Journal of Wildlife Diseases 2000;36:111-123.). These studies have described themorphological characteristics of hematologicalcells. Erythrocytes were ovoid cells with an ovoid nucleus composed of dense chromatin and homogeneous eosinophilic cytoplasm. The “ovoid” shape varies between species with some species having noticeably rounded cells whereas other species have a narrower, elongated shape. Mature avian erythrocytes are elliptical and have an elliptical, centrally positioned nucleus (Campbell, 2015Campbell TW. Exotic animal hematology and cytology. 4th ed. Colorado: John Wiley & Sons; 2015.). Avian mature erythrocytes are generally larger than mammalian erythrocytes but smaller than reptilian erythrocytes (Sturkie & Griminger, 1986).

In most species of birds, erythrocyte shape is relatively uniform, however, the shape of the red blood cells may be somewhat variable (Campbell, 2015Campbell TW. Exotic animal hematology and cytology. 4th ed. Colorado: John Wiley & Sons; 2015.). Variations in erythrocyte morphology occur in blood films from healthy birds as well as those with medical disorders. Therefore, atypical erythrocytes may vary in both size and shape. A significant change in the mean size of the erythrocyte is reflected in the mean corpuscular volume (MCV). A slight variation in the size of erythrocytes is considered in healthy birds. Flight less birds like the ostrich have the largest erythrocytes whereas the higher evolved good fliers, like passerines, tend to have smaller erythrocytes (Maina, 1996Maina JN. Perspectives on the structure and function of birds. In: Rosskopf W, Woerpel R, editors. Diseases of cage and aviary birds. 3rd ed. Baltimore: William & Wilkins; 1996.; Welty, 1982Welty JC. Skin scales, feathers and colours. The life of birds. 3rd ed. Philadelphia: Saunders College Publishing; 1982.). Erythrocyte subpopulations have been reported in ducks, in which larger erythrocytes (MCV, 308 fL/cell) most likely represent those most recently released from the hematopoietic tissue and smaller cells (MCV, 128 fL/cell) most likely represent the older, aging cells (Herbert et al., 1989). Reticulocytes are the penultimate cell in the erythrocyte maturation series, and their presence in the peripheral blood of healthy birds suggests that the final stages of red-cell maturation occur in circulating blood. Reticulocytes tend to be smaller in size and less elongated compared to the mature erythrocyte (Campbell, 2015). Changes that typically occur in the size of avian erythrocytes include microcytosis, macrocytosis and anisocytosis. A greater degree of anisocytosis, however, usually is observed in birds with a regenerative anemia and is associated with polychromasia. Likewise, minor deviations from the normal shape of avian erythrocytes are considered to be normal in the peripheral blood of birds, but marked poikilocytosis may indicate erythrocytic dysgenesis (Campbell, 2015). The degree of variation in the size of erythrocytes anisocytosis can be scored from 1+ to 4+ based on the number of variable-sized erythrocytes in a monolayer field (Weiss, 1984Weiss DJ. Uniform evaluation and semiquantitative reporting of hematologic data in veterinary laboratories. Veterinary Clinical Pathology 1984;13(2):27-31.). Food restriction anemia is also associated with a leukopenia, thrombocytopenia, abnormal erythrocyte shapes (marked poikilocytosis) and hypersegmentation of granulocytes (Maxwell et al., 1991Maxwell MH, Robertson GW, Anderson IA, Dick LA, Lynch M. Haematology and histology of seven-week old broilers after early food restriction. Research in Veterinary Science 1991;50:290-297.). Erythrocytes with variant morphology may be evident, depending on the cause of the anemia and the hematological response (Clark et al., 2009Clark P, Boardman W, Raidal S. Atlas of clinical avian hematology. Oxford; Wiley-Blackwell; 2009.). Microcytic, hypochromic, nonregenerative anemia is often associated with chronic inflammatory diseases in birds, especially those with an infectious etiology (Tell et al., 2004Tell LA, Ferrell ST, Gibbons PM. Avian mycobacteriosis free-living raptors in California: 6 cases. Journal of Avian Medicine and Surgery 2004;18:30-40.). The presence of hemoparasites such as Haemoproteus spp. and Plasmodium spp. may alter the morphology of erythrocytes. The presence of the organism may distort the shape of the cell, enlarge the size of the cell, or displace the nucleus within the cell (Clark et al., 2009).

The aim is to study the morphometric parameters of erythrocytes in juvenile Mandarin ducks Aix galericulata. The morphometric parameters of erythrocytes in Mandarin ducks have never been subjected to study even though this species is common in aviculture. Due to insufficient research and disadvantages of scientific papers from this scientific field, the knowledge about the morphometric parameters of erythrocytes in Mandarin ducks- Aix galericulata represent the beginning of hematological studies on the mandarin ducks. Although numerous quick and simple methods for determination of qualitative and quantitative hematological values exist today, analysing the peripheral blood smears can be valuable when it comes to the species that haven’t been yet studied extensively. The influence of different factors such as sex, mutation, age and reproductive status is proven to have impact on the hematological values of Mandarin ducks, as well as on the hematological values of other bird species. The influence of these factors on a species such as the Mandarin duck, that is still not considered domesticated, in aviculture, needs to be subjected to more detailed studies.

MATERIAL AND METHODS

The study was conducted in January 2018 and the blood smears from juvenile Mandain ducks- Aix galericulata were taken from thirty Mandarin ducks which were six months old at the time. Blood samples from the normal (standard/wild colour), white and apricot Mandarin ducks were collected by puncturing the wing vein- Vena ulnaris cutanea using sterile needles and syringes and following the aseptic principles, according to authors (Janig et al., 2017). Blood samples from all Mandarin ducks were taken during the process of National program of animal health strategy, which is determined by the Ministry of agriculture, forestry and water managment Republic of Serbia. No bird was harmed during this process.

Total blood volume for birds is usually about 6-8 ml per 100g body mass (Sturkie et al., 1986). We extracted 0.5 ml of blood from each Mandarin duck which would be about 0.2% of the total blood volume. Immediately after vein puncture and extracting 0,5 ml of each bird’s blood, a few drops of blood without anticoagulants were transferred into microscope slides and the blood smears were made. These were dried promptly and stored until prepared for study in the laboratory. The smears were stained using Diff-Quik® stain method. After being dried, blood smears were observed under a microscope and the images were made. In this research 1500 morphometric parameters of erythrocytes were obtained from blood samples of thirty Mandarin ducks. According to the instructions of the authors (Janiga et al., 2017) from each individual blood smear, from the thirty blood smears obtained, fifty erythrocytes were randomly chosen, whose morphometric parameters, or more precisely, the length and width of erythrocytes were calculated by using ImageJ, a public domain, Java-based image processing program developed at the National Institutes of Health.

RESULTS

This study is based on the morphometric parameters of 1500 measured erythrocytes which are obtained from blood smears of thirty Mandarin ducks. The length and width of each of the 1500 erythrocytes were determined and expressed in micrometers (µm) (Fig. 1 and 2). The average length of the measured erythrocytes was 11.879 µm. The average width of the measured erythrocytes was 6.160 µm (Table 1). The maximal measured length of the erythrocytes was 16.049 µm whereas the minimal measured length was 5.668 µm. The maximal measured width of the erythrocytes was 10.115 µm and the minimal measured width was 3.750 µm (Fig. 3). The average ratio of length to width of erythrocytes was 1.996.

Figure 1
Display of measuring length erythrocyte in Mandarin ducks using the ImageJ program. Following the random selection of each individual erythrocyte, using the ImageJ program, a line that measures the length of the erythrocyte, the value of measured erythrocyte lenght was obtained.

Figure 2
Display of measuring width of singular erythrocyte in Mandarin ducks using the ImageJ program. Following the random selection of each individual erythrocyte, using the ImageJ program, a line that measures the width of the erythrocyte, the value of the measured erythrocyte width was obtained.

Table 1
Average values of morphometric parameters of Mandarin duck’s Aix galericulata erythrocytes

Figure 3
Extreme (maximal and minimal) length and width of the measured erythrocytes of Mandarin duck’s Aix galericulata.

DISCUSSION

Autors Hartman & Lasser (1963Hartman FA, Lessler MA. Erythrocyte measurments. In: Birds F A. Hartman and M. A. Lessler The Auk 1963;80(4):467-473.) in their research of birds erythrocytes, have measured average ratio of length and width of erythrocyte. The highest value of average ratio of length and width was 2.11 µm and it was recorded forth especies Cardellinapusilla, while the lowest value of average ratio of length and width was 1.62 µm and it was recorded forth especies Turdusplebejus and Thraupisepiscopus. In this research, average value of this ratio in erythrocytes of Mandarin duck was 1.99 µm.

According to Rusov (2002Rusov C. Hematologijaptica. Beograd: Naucniinstitut za veterinarstvo Srbije; 2002.), the erythrocytes in peripheral blood smears have a 10.7-15.5μm long and 2.64-2.25 μm wide diameter, depending on bird species. The average length of Mandarin ducks’ erythrocytes determined in this study corresponds to the values that Rusov (2002) described. However, the average width of the measured erythrocytes was 6.160 µm and it is almost three times larger than what he described.

Avian erythrocytes vary in size depending on the species, but they generally range between 10.2- 15.8 μm and 6.1-10.7 μm (Sturkie & Griminger, 1986). Their results correspond to the results of this study of morphometric parameters of erythrocytes in Mandarin ducks with the length of erythrocytes - 11.879 μm and width - 6.160 μm.

According to Tadjalli et al. (2003Tadjalli M, Nazifi S, Eemanparvar A. Normal cellular morphology of the blood of Japanese quail (Coturnix coturnix japonica). Comparative Clinical Pathology 2003;12:102-105.) measures of adult Coturnix quail erythrocytes were 11.06 ± 0.70 μm in length and 6.80 ± 0.67μm in width in males and 11.40 ± 0.63 μm in length and 6.73 ± 0.45 μm in width in females. The results of this study are almost the same as the results of the study that Tadjalli et al. (2003) performed, although the blood smears weren’t divided according to the ducks’ sex. But according to Sturkie & Griminger, (1986) measures of adult Coturnix quail erythrocytes were 9.80 ± 0.77μm in length and 8.23 ± 0.72 μm in width in males and 9.80 ± 0.77 μm in length and 7.73 ± 0.70 μm in width in females. When compared to the results in this study, it’s clear that the erythrocytes in Coturnix quail (regardless of the sex of the quails) are significantly smaller in size than the erythrocytes in Mandarin ducks.

According to Biester & Schwarte (1955Biester HE, Schwarte LH. Bolestiperadi. Zagreb: Poljoprivredninakladnizavod;1955.), the average length of chickens’ erythrocytes is 12.2 μm and the average width is 7.3 μm. When compared to the results of this study, the values are similar, as the average length of Mandarin ducks’ erythrocytes is 11.879 μm and the average width of Mandarin ducks’ erythrocytes is 6.160 μm.

Comparison of birds with their ancestral relatives, the reptiles, shows how great the divergence is between these groups. According to Wintrobe (1961Wintrobe M. Clinical hematology. Philadelphia: Lea and Febiger;1961.), reptilian erythrocytes range from 18.1-8.7 μm (turtle) to 23.2- 12.1 μm (alligator). These differences indicate how far ahead on the metabolic scale the birds are and also Mandarin duck with average length of erythrocytes 11.87μm and the average width erythrocytes 6.16 μm.

Comparison of the erythrocytes of birds with other warm-blooded animals is interesting. In mammals their diameters range from 5- 6 μm in horse, cow, pig, mouse and rat, to 7-7.4 μm in chimpanzee, woodchuck and llama (Wintrobe, 1961Wintrobe M. Clinical hematology. Philadelphia: Lea and Febiger;1961.). This author’s results compared to the results of this study show that birds have larger erythrocytes than mammals.

Seasonal variations, age and species affect the erythrocyte parameters of healthy birds, especially wildlife (Harper & Lowe, 1998Harper EJ, Lowe B. Hematology values in a colony of budgerigars (Melopsittacusundulatus) and changes associated with aging. Journal of Nutrition 1998;28:2639S-2640S.; Hauptmanova et al., 2006Hauptmanova K, Maly M, Literak I. Changes of haematological parameters in common pheasant throughout the year. Vet Med 2006;51:29034.; Rehder et al., 1982Rehder NB, Lague DM, Mackay C. Variation in selected hematological parameters of captive red-tailed hawks. Journal of Wildlife Diseases 1982;18:105-109.; Schmidt et al., 2007Schmidt EMDS, Paulillo AC, Dittrich RL. The effect of age on hematological and serum biochemical values in juvenile ring-necked pheasants (Phasianuscolchicus). International Journal of Poultry Science 2007;6:459-461.; Shave & Howard, 1976Shave HJ, Howard V. A hematologic survey of captive waterfowl. Journal of Wildlife Diseases 1976;12:195-201.). These authors’ claims can be compared to the results of this study as all the birds were of the same age and under the same climate conditions. The above-mentioned factors can be linked to the determined minimal and maximal length (5.66 μm and 16.04 μm) and minimal and maximal width (10.11 μm and 3.75 μm) of erythrocytes in Mandarin ducks.

Age can be a cause of variation in the normal hemogram of healthy ducklings. Difference in hematologic parameters likely including erythrocytes associated with the high metabolic rate of young rapidly growing ducks that are consuming diets higher in protein and carbohydrates (Kocan & Pitts, 1976Kocan RM, Pitts SM. Blood values of the canvasback duck by age, sex and season, Journal of Wildlife Diseases 1976;12:341-345.). Some studies have shown that averages for erythrocyte parameters tend to be higher in the winter and pre-nesting period in adult ducks and geese regardless of gender compared to the post-nesting period and fall (Williams & Trainer, 1971Williams JI, Trainer DO.A hematological study of snow, blue, and Canada geese. Journal of Wildlife Diseases 1971;7:258-265.; Shave & Howard, 1976Shave HJ, Howard V. A hematologic survey of captive waterfowl. Journal of Wildlife Diseases 1976;12:195-201.). Although the results of this study represent the first data on the erythrocytes of the Mandarin ducks, they can be compared to these authors’ results as the blood samples were taken during the winter season, two months before the reproductive season for these birds started.

CONCLUSION

Erythrocytes, as the most numerous blood cells, represent one of the basic indicators of health condition in birds. Making of blood smears is a simple and practical method used to determine various pathological processes inside birds’ organism, caused by erythrocytes size change. Knowing morphometric parameters of Mandarin duck erythrocytes is the first step in the evaluation process of erythrocytes’ functional state and health condition of an individual.

REFERENCES

  • Biester HE, Schwarte LH. Bolestiperadi. Zagreb: Poljoprivredninakladnizavod;1955.
  • Clark P, Boardman W, Raidal S. Atlas of clinical avian hematology. Oxford; Wiley-Blackwell; 2009.
  • Driver EA. Hematological and blood chemical values of mallard, Anas platyrhynchos, drakes before, during and after remigemoult. Journal of Wildlife Diseases 1981;17:413-421.
  • Campbell TW. Exotic animal hematology and cytology. 4th ed. Colorado: John Wiley & Sons; 2015.
  • Fairbrother A, O'Loughlin D. Differential white blood cell values of the mallard (Anas platyrhynchos) across different ages and reproductive states. Journal of Wildlife Diseases 1990;26:78-82.
  • Fairbrother A, Craig MA, Walker K, O'Loughlin D. Changes in mallard (Anas platyrhynchos) serum chemistry due to age, sex, and reproductive condition. Journal of Wildlife Diseases 1990;26:67-77.
  • Harper EJ, Lowe B. Hematology values in a colony of budgerigars (Melopsittacusundulatus) and changes associated with aging. Journal of Nutrition 1998;28:2639S-2640S.
  • Hartman FA, Lessler MA. Erythrocyte measurments. In: Birds F A. Hartman and M. A. Lessler The Auk 1963;80(4):467-473.
  • Hauptmanova K, Maly M, Literak I. Changes of haematological parameters in common pheasant throughout the year. Vet Med 2006;51:29034.
  • Kocan RM, Pitts SM. Blood values of the canvasback duck by age, sex and season, Journal of Wildlife Diseases 1976;12:341-345.
  • Levengood JM, Sanderson GC, Anderson WL, Foley GL, Brown PW, Seets JW. Influence of diet on the hematology and serum biochemistry of zinc-intoxicated mallards. Journal of Wildlife Diseases 2000;36:111-123.
  • Maina JN. Perspectives on the structure and function of birds. In: Rosskopf W, Woerpel R, editors. Diseases of cage and aviary birds. 3rd ed. Baltimore: William & Wilkins; 1996.
  • Maxwell MH, Robertson GW, Anderson IA, Dick LA, Lynch M. Haematology and histology of seven-week old broilers after early food restriction. Research in Veterinary Science 1991;50:290-297.
  • Mulley RC. Haematology and blood chemistry of the black duck (Anas supercilliosa). Journal of Wildlife Diseases 1979;15:473-441.
  • Mulley RC. Haematology of the wood duck Chenonettajubata. Journal of Wildlife Diseases 1980;16:271-273.
  • Rehder NB, Lague DM, Mackay C. Variation in selected hematological parameters of captive red-tailed hawks. Journal of Wildlife Diseases 1982;18:105-109.
  • Rusov C. Hematologijaptica. Beograd: Naucniinstitut za veterinarstvo Srbije; 2002.
  • Schmidt EMDS, Paulillo AC, Dittrich RL. The effect of age on hematological and serum biochemical values in juvenile ring-necked pheasants (Phasianuscolchicus). International Journal of Poultry Science 2007;6:459-461.
  • Shave HJ, Howard V. A hematologic survey of captive waterfowl. Journal of Wildlife Diseases 1976;12:195-201.
  • Sturkie PD, Griminger P. Avian physiology. In: Sturkie PD, editor. Body fluids: blood. 4th ed. New York: Springer; 1976.
  • Tadjalli M, Nazifi S, Eemanparvar A. Normal cellular morphology of the blood of Japanese quail (Coturnix coturnix japonica). Comparative Clinical Pathology 2003;12:102-105.
  • Tell LA, Ferrell ST, Gibbons PM. Avian mycobacteriosis free-living raptors in California: 6 cases. Journal of Avian Medicine and Surgery 2004;18:30-40.
  • Weiss DJ. Uniform evaluation and semiquantitative reporting of hematologic data in veterinary laboratories. Veterinary Clinical Pathology 1984;13(2):27-31.
  • Welty JC. Skin scales, feathers and colours. The life of birds. 3rd ed. Philadelphia: Saunders College Publishing; 1982.
  • Williams JI, Trainer DO.A hematological study of snow, blue, and Canada geese. Journal of Wildlife Diseases 1971;7:258-265.
  • Wintrobe M. Clinical hematology. Philadelphia: Lea and Febiger;1961.

Publication Dates

  • Publication in this collection
    14 Nov 2019
  • Date of issue
    2019

History

  • Received
    14 Feb 2018
  • Accepted
    09 Jan 2019
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