Langyu Gu, Hanyu Yang, Canwei Xia, Zitan Song, Yachang Cheng, Chenjing Huang, Yuelou Liu, Yang Liu. 2023: Comparisons of microstructure and elemental composition of eggshells among wild plover populations. Avian Research, 14(1): 100146. DOI: 10.1016/j.avrs.2023.100146
Citation: Langyu Gu, Hanyu Yang, Canwei Xia, Zitan Song, Yachang Cheng, Chenjing Huang, Yuelou Liu, Yang Liu. 2023: Comparisons of microstructure and elemental composition of eggshells among wild plover populations. Avian Research, 14(1): 100146. DOI: 10.1016/j.avrs.2023.100146

Comparisons of microstructure and elemental composition of eggshells among wild plover populations

Funds: 

the Science and Technology Projects in Guangzhou 202102020231

YL was funded by the Forestry Administration of Guangdong Province, China DFGP Project of Fauna of Guangdong-202115

YL was funded by the Forestry Administration of Guangdong Province, China Science and Technology Planning Projects of Guangdong Province-2021B1212110002

More Information
  • Corresponding author:

    E-mail address: liuy353@mail.sysu.edu.cn (Y. Liu)

  • 1 These authors contributed equally to this work.

  • Received Date: 10 Jul 2023
  • Rev Recd Date: 04 Oct 2023
  • Accepted Date: 29 Oct 2023
  • Available Online: 10 Jan 2024
  • Publish Date: 05 Nov 2023
  • Reproduction investment is a prominent trade-off in life-history theory and is subject to strong selection pressure. The avian eggshell, as a crucial barrier between the bird embryo and the surrounding environment, undergoes optimization under different environmental selection regimes to ensure the successful development of embryos, which can be linked to local adaptation. Therefore, understanding the variation in eggshell microstructure and composition in wild bird populations living in contrasting ambient environments is of great significance. In this study, we utilized electron microscope ultrastructure measurement and elemental analyses to measure and compare the microstructure and element composition of eggshells from three wild plover populations (Charadrius alexandrinus and C. dealbatus) residing in heterogeneous habitats across varied climatic zones. These populations include the high-altitude Qinghai Lake population, the temperate coastal Tangshan population, and the tropical coastal Zhanjiang population. Our findings revealed that the palisade layer was thinner in the Qinghai Lake population compared to its lowland populations. This difference might be attributed to hypoxia which facilitates the hatching process by allowing chicks to easily break through their shells. Additionally, the variations in the elemental composition of the eggshells among populations well reflected the distribution of element content in different geographical regions. The Qinghai Lake population displayed low zinc and low manganese levels but high calcium levels, while the Zhanjiang population exhibited high zinc, high iron, high manganese, and high phosphorus levels. Furthermore, these variations in elemental composition could also account for the observed microstructural differences among populations. Collectively, we propose that the dissimilarities in eggshell microstructure and elemental composition among populations could be attributed to adaptations to different environmental conditions. Our findings lay the groundwork for future research to explore the mechanisms behind the variations in eggshell characteristics among wild bird populations, and contribute to a broader understanding of biodiversity mechanisms.

  • Pollution of the natural environment by heavy metals is a worldwide problem. Heavy metals enter the aquatic ecosystem through a variety of anthropogenic sources as well as from natural processes (Ebrahimpour and Mushrifah, 2010). They are a serious threat because of their toxicity, bioaccumulation, long persistence and bio-magnification in the food chain (Erdoĝrul and Ates, 2006). The degree of toxic metal uptake, translocation and eventual detoxification within an organism depends on metal speciation, but also differs strongly among organisms (Mukherjee and Nuorteva, 1994; Doyle and Otte, 1997). Assessing ecosystem health adequately by means of biomonitoring requires the selection of representative indicator species. Birds are widely used to biomonitoring variation in environmental levels of anthropogenic pollutants (Furness and Camphuysen, 1997; Barbieri et al., 2009), because they are exposed to a wide range of chemicals and occupy high trophic levels and can therefore provide information on the extent of contamination in the entire food chain (Furness and Camphuysen, 1997; Burger et al., 2007).

    According to Burger and Gochfeld(2000a, 2000b) feathers are useful for measuring heavy metal contamination in birds because birds sequester heavy metals in their feathers, where the proportion of the body burden is relatively constant for each metal. In general, metals in breast feathers are representative of circulating concentrations in the blood stream only during the limited time period of feather formation, which in turn represents both local exposure and mobilization from internal tissues (Lewis and Furness, 1991; Monteiro, 1996). Many studies have recommended herons and egrets as bioindicators for heavy metals in aquatic systems and local pollution around breeding sites (Boncompagni et al., 2003; Kim and Koo, 2007). Herons and gulls are high at the top of their food pyramid and can yield information over a large area around each sampling site, not only on bioavailability of contaminants but also on how, where, and when they are transferred within the food web (Battaglia et al., 2005). Hence, the aim of the present study was to investigate the level of nickel in feathers of two bird species, the Western Reef Heron (Egretta gularis) and the Siberian Gull (Larus heuglini), in order 1) to compare metal concentrations between two species with their life strategy and 2) to examine the species and gender related variation in trace nickel accumulations in the Hara Biosphere Reserve of southern Iran.

    The Hara Biosphere Reserve (26°40′–27°N, 55°21′–55°52′E) is located in southern Iran, in the Straits of Khuran between Queshm Island and the Persian Gulf (Fig. 1). This area became part of the Man and Biosphere Program (MAB) of UNESCO in 1977 (UNESCO, 2010). As well, this region is one of the protected areas in Iran introduced by the Department of the Environment. The entire region was selected as wetland of international importance under the Wetlands of International Importance category as a Habitat of Aquatic Birds. This region was also introduced as one of the important bird areas by the International Organization of Birdlife (Neinavaz et al., 2010).

    Figure  1.  Location of the Hara Biosphere Reserve in southern Iran

    During November and December 2010, under license of the Environmental Protection Agency of Hormozgan, a total of thirty birds were shot and removed from throughout the Hara biosphere reserve. The collection included the Western Reef Heron (Egretta gularis) (n = 15) and the Siberian Gull (Larus heuglini) (n = 15). The birds were transported to the laboratory packed in ice. The specimen were killed, weighed, stored in plastic bags and kept at −20℃ until dissection and analysis. We chose breast feathers because they are representatives of the plumage and are less affected by molt compared to flight feathers. All feathers were analyzed in the Laboratory of the Inland Water Aquaculture Research Institute in port Anzali. The feather samples were digested in a nitric acid (HNO3) and perchloric acid (HClO4) mixture. Feathers were then accurately weighed in 150-mL Erlenmeyer flasks, where 10 mL nitric acid (65%) was added to each sample. The samples were left overnight to be slowly digested; thereafter, 5 mL perchloric acid (70%) was added to each sample. Digestion was performed on a hot plate (sand bath) at 200℃. After that, the digested samples were diluted by 25 mL deionized water. The concentration of nickel was estimated using a Shimadzu AA 680 flame atomic absorption spectrophotometer. The accuracy of the analysis was checked by measuring CRM certified reference tissue (DORM-2, NRC Canada). The detection limit for nickel was 0.039 µg·g−1. The results for nickel gave a mean recovery of 98.6%.

    A statistical analysis was carried out using SPSS (version 18.0). We used a three-way ANOVA for nickel (sex, age, species, interaction (sex × age × species)). Data were log transformed to obtain normal distributions that satisfied the homogeneity of variance required by ANOVA (Custer et al., 2003; Kim et al., 2009). The nickel concentration in feathers was tested for mean differences between species using Student t tests. The level of significance was set at α = 0.05. The concentration of nickel in feathers was expressed in microgram per gram of dry weight (dw). Values are given in means ± standard errors (SE).

    Variations in the nickel concentration of feathers of the Western Reef Heron and Siberian Gull are presented in Table 1. The results show that there was a significant difference between the mean nickel concentrations in the two bird species, i.e. the Western Reef Heron and Siberian Gull, while there was no evidence of significant different accumulation between genders and ages (Table 2). Also, the results indicate that the level of nickel concentration in the Western Reef Heron was higher in females than in males; in contrast, the level of nickel concentration in the Siberian gull was higher in males.

    Table  1.  Geometric means (95% CI) nickel concentrations in feathers of Western Reef Heron and Siberian Gull from the Hara Biosphere Reserve of southern Iran
    Species Male/adult Male/juvenile Female/adult Female/juvenile
    Western Reef Heron
    Geometric mean 2.77 3.79 4.67
    Mean ± SE 3.47±2.7 4.67±2.7 4.67
    Number 9/9 5/5 1
    Siberian Gull
    Geometric mean 8.89 3.87 6.72 7.24
    Mean ± SE 8.94±1.1 4.38±2.5 7.6±3.4 8.1±4.8
    Number 3/3 3/3 6/6 3/3
     | Show Table
    DownLoad: CSV
    Table  2.  Analysis of variance (ANOVA) of nickel concentrations among species, gender and age
    Source of variation Mean square F p
    Species 78.23 8.56 0.01 a
    Gender 9.56 1.04 NS b
    Age 7.57 0.82 NS
    Intercept (species × gender × age) 572.55 62.66 0.001
    a p-value for 3-way ANOVA. Interaction term significant as indicated.
    b NS = not significant at p > 0.05.
     | Show Table
    DownLoad: CSV

    Nickel is not an important trace element in organisms, but at high levels, they can cause adverse health effects. Sources of heavy metals vary considerably. It is emitted into the environment by both natural and man-made sources. Once released into the environment, nickel readily forms complexes with many ligands, making it more mobile than most heavy metals (Mansouri et al., 2011). Nickel is related to the pigmentation of feathers in birds and excreted via the feathers by moulting (Honda et al., 1986). Nickel concentrations in the current study (3.47–8.94 µg·g−1) were higher than those in Fulica atra (0.8 µg·g−1), Phalacrocorax carbo (0.5 µg·g−1) and Nycticorax nycticorax (1.2 µg·g−1) from Russia (Lebedeva, 1997), in Egretta alba (0.2 µg·g−1) from Korea (Honda et al., 1986) and Parus major (0.25 µg·g−1) from China (Deng et al., 2007). In our study, the nickel concentrations were similar to those in Bubulcus ibis L. (7.8–9.0 µg·g−1) from Pakistan (Malik and Zeb, 2009).

    Few studies have examined the effect of gender on the accumulation of heavy metals in feathers and other tissues (Burger, 1995; Zamani-Ahmadmahmoodi et al., 2010). Several studies reported no significant differences in the heavy metal content of feathers between male and female birds (Hutton, 1981; Zamani-Ahmadmahmoodi et al., 2009a). Similarly, in the present study there was no evidence of significant different accumulations between male and female birds (Table 2), suggesting that both sexes utilize similar foraging strategies in both species (Hindell et al., 1999). While studying heavy metals in the feathers of Larus dominicanus, Barbieri et al. (2009) showed that the levels of nickel concentration were higher in adults (5.92 µg·g−1) than in juveniles (2.23 µg·g−1). Similar levels of nickel have been detected in other seabird species from different parts of the world (Norheim, 1987). Adults have had several years to accumulate metals in their internal tissues; these can be mobilized into the blood and deposited in feathers during their formation (Burger, 1994). Elsewhere, Burger and Gochfeld (1991) pointed to heavy metal concentrations in feathers of adult birds that may reflect exposure obtained at other time of the year, including exposure at non-breeding areas. On the other hand, while they were studying heavy metal concentrations in the feathers of Herring Gulls (Larus argentatus) in Captree, Long Island, they showed that the cadmium concentration was higher in juveniles but the lead concentration was higher in adults (Burger, 1995). Differences in levels of metal concentrations in adults and fledglings might also occur if adults and young eat different types of food during the breeding season, or different-sized food items (Burger, 1996).

    Research has indicated that the concentration of heavy metals in the tissues of migratory birds is higher than that in resident birds (Pacyna et al., 2006; Zamani-Ahmadmahmoodi et al., 2009b). Siberian Gulls are winter visitors to Hara Biosphere Reserve, while Western Reef Heron are residents there. The results of the current study show that the amount of nickel in the Siberian Gull feathers is higher than in the Western Reef Heron.

    The results of three-way ANOVA showed there were significant differences between the Western Reef Heron and Siberian Gull (p < 0.01). The Siberian Gull showed higher nickel concentrations than the Western Reef Heron. Birds that are large fish eaters should accumulate higher levels than those that eat a range of different foods or smaller fish. Furthermore, levels of metal in birds should reflect the levels in the fish they consume (Burger, 2002). The main difference in nickel levels between Western Reef Heron and Siberian Gull could be the result of different phylogenetic origin and physiology (Teal, 1969; Welty, 1975; Deng et al. 2007), or because they grow their feathers in different breeding areas with different levels of background contamination. Also, metabolic rates vary inversely with body weight and directly with activities such as flight and rest. Being smaller than Western Reef Heron, Siberian Gull was expected to have a higher metabolic rate. Higher metabolic rates may cause fast accumulations of trace nickel in the Siberian Gull. In general, the Siberian Gull eats more invertebrates than the Western Reef Heron, catches some larger fish (between 20–25 cm in size), consumes offal discarded by fishing boats and eats dead fish found along the shore, while the Western Reef Heron eats smaller fish, amphibians and insects.

  • Alrashidi, M., Kosztolányi, A., Küpper, C., Cuthill, I.C., Javed, S., Székely, T., 2010. The influence of a hot environment on parental cooperation of a ground-nesting shorebird, the Kentish plover Charadrius alexandrinus. Front. Zool. 7, 1.
    Ar, A., Rahn, H., 1985. Pores in avian eggshells: gas conductance, gas exchange and embryonic growth rate. Respir. Physiol. 61, 1–20.
    Arad, Z., 1989. Changes in eggshell water vapour conductance during shell formation in the chicken. Respir. Physiol. 78, 197–206.
    Archer, G.S., 2019. How does red light affect layer production, fear, and stress? Poultry Sci. 98, 3–8.
    Bebout, D.E., Hempleman, S.C., 1994. Calcium deficient diet, acetazolamide and gas exchange characteristics of avian eggshells. Respir. Physiol. 95, 11–20.
    Bleu, J., Agostini, S., Angelier, F., Biard, C., 2019. Experimental increase in temperature affects eggshell thickness, and not egg mass, eggshell spottiness or egg composition in the great tit (Parus major). Gen. Comp. Endocrinol. 275, 73–81.
    Cao, H., Deng, Y., Chen, F., Pu, X., 2020. Analysis of trace element characteristics and ecological risk assessment in the surface of sediments in the Zhanjiang Bay. J. Ocean Technol. 2, 71–77.
    Chang, G., Liu, N., Yang, W., Zhong, R., Ren, H., 2020. Characteristics and influencing factors of heavy metals in Tangshan Coastal environment. Front. Earth Sci. 10, 1042–1050.
    Chien, Y.-C., Hincke, M.T., McKee, M.D., 2009. Ultrastructure of avian eggshell during resorption following egg fertilization. J. Struct. Biol. 168, 527–538.
    Chien, Y.C., Hincke, M.T., Vali, H., McKee, M.D., 2008. Ultrastructural matrix-mineral relationships in avian eggshell, and effects of osteopontin on calcite growth in vitro. J. Struct. Biol. 163, 84–99.
    Dauphin, Y., Luquet, G., Perez-Huerta, A., Salomé, M., 2018. Biomineralization in modern avian calcified eggshells: similarity versus diversity. Connect. Tissue Res. 59, 67–73.
    Dieckert, J.W., Dieckert, M.C., Creger, C.R., 1989. Calcium reserve assembly: a basic structural unit of the calcium reserve system of the hen egg shell. Poultry Sci. 68, 1569–1584.
    Ding, J., Yang, W., Yang, Y., Ai, S., Bai, X., Zhang, Y., 2019. Variations in tree sparrow (Passer montanus) egg characteristics under environmental metal pollution. Sci. Total Environ. 687, 946–955.
    Ebeid, T.A., Suzuki, T., Sugiyama, T., 2012. High ambient temperature influences eggshell quality and calbindin-D28k localization of eggshell gland and all intestinal segments of laying hens. Poultry Sci. 91, 2282–2287.
    Flatt, T., Heyland, A., 2011. Mechanisms of Life History Evolution : the Genetics and Physiology of Life History Traits and Trade-Offs. Oxford University Press, Oxford.
    Gongruttananun, N., 2011. Influence of red light on reproductive performance, eggshell ultrastructure, and eye morphology in Thai-native hens. Poultry Sci. 90, 2855–2863.
    Halgrain, M., Bernardet, N., Crepeau, M., Même, N., Narcy, A., Hincke, M., et al., 2022. Eggshell decalcification and skeletal mineralization during chicken embryonic development: defining candidate genes in the chorioallantoic membrane. Poultry Sci. 101, 101622.
    Hempleman, S.C., Adamson, T.P., Bebout, D.E., 1993. Oxygen and avian eggshell formation at high altitude. Respir. Physiol. 92, 1–12.
    Huang, L., Shen, J., Feng, Y., Li, D., Wang, W., Yang, L., et al., 2020. Effect of dietary zinc level on egg production performance and eggshell quality characteristics in laying duck breeders in furnished cage system. Biol. Trace Elem. Res. 196, 597–606.
    Hung, C.-M., Tsao, S.-H., Chiang, P.-L., Wu, S.-P., Tuanmu, M.-N., Juang, J.-Y., 2022. Functional connections between bird eggshell stiffness and nest characteristics through risk of egg collision in nests. Ecol. Lett. 25, 1421–1431.
    Jetz, W., Sekercioglu, C.H., Böhning-Gaese, K., 2008. The worldwide variation in avian clutch size across species and space. PLoS Biol. 6, 2650–2657.
    Kamanlı, S., Demirtaş, Ş. E., Onbaşılar, E.E., Bakır, B., Yalçın, S., Göğer, H., et al., 2021. The effects of the breeder index value on the microscopic structure of egg shells, hatching results, and hybrid performance. Trop. Anim. Health Prod. 53, 557.
    Karlsson, O., Lilja, C., 2008. Eggshell structure, mode of development and growth rate in birds. Zoology (Jena) 111, 494–502.
    Kim, J.H., Kim, H.W., Kwon, C.H., Kwon, S.H., Kil, D.Y., 2023. Effects of dietary organic or inorganic iron concentrations on productive performance, egg quality, blood measurements, and tissue iron concentrations in aged laying hens. Anim. Sci. J. 94, e13817.
    Kosztolányi, A., Székely, T., Cuthill, I.C., Yilmaz, K.T., Berberoglu, S., 2006. Ecological constraints on breeding system evolution: the influence of habitat on brood desertion in Kentish plover. J. Anim. Ecol. 75, 257–265.
    Lee, J., McCurdy, C., Chae, C., Hwang, J., Karolak, M.C., Kim, D.-H., et al., 2021. Myostatin mutation in Japanese quail increased egg size but reduced eggshell thickness and strength. Animals 12, 47.
    Liao, X., Yan, J., Chen, J., Huang, Z., Xiao, T., Li, C., et al., 2022. A simple daily dynamic feeding regimen for reducing phosphorus consumption and excretion in laying hens. Anim. Nutr. 11, 132–141.
    Liu, J., Chai, Z., Wang, H., Ivanov, A., Kubelka, V., Freckleton, R., et al., 2023. Effects of feeding strategies on eggshell quality of laying hens during late laying period. Poultry Sci. 102, 102406.
    Mayer, A.N., Vieira, S.L., Berwanger, E., Angel, C.R., Kindlein, L., França, I., et al., 2019. Zinc requirements of broiler breeder hens. Poultry Sci. 98, 1288–1301.
    McClelland, S.C., Cassey, P., Maurer, G., Hauber, M.E., Portugal, S.J., 2021. How much calcium to shell out? Eggshell calcium carbonate content is greater in birds with thinner shells, larger clutches and longer lifespans. J. R. Soc. Interface 18, 20210502.
    Nakagawa, S., Schielzeth, H., 2017. rptR: repeatability estimation and variance decomposition by generalized linear mixed-effects models. Methods Ecol. Evol. 8, 1639–1644.
    Orłowski, G., Siebielec, G., Kasprzykowski, Z., Dobicki, W., Pokorny, P., Wuczyński, A., et al., 2016. Effect of spatial resolution of soil data on predictions of eggshell trace element levels in the Rook Corvus frugilegus. Environ. Pollut. 219, 288–295.
    Peebles, E.D., Brake, J., Gildersleeve, R.P., 1987. Effects of eggshell cuticle removal and incubation humidity on embryonic development and hatchability of broilers. Poultry Sci. 66, 834–840.
    Reynolds, S.J., Perrins, C.M., 2010. Dietary calcium availability and reproduction in birds. In: Current Ornithology, 17. Springer, New York, NY, pp. 31–74.
    Solomon, S.E., 2010. The eggshell: strength, structure and function. Br. Poultry Sci. 51(Suppl. 1), 52–59.
    Song, Z., Lin, X., Que, P., Halimubieke, N., Huang, Q., Zhang, Z., et al., 2020. The allocation between egg size and clutch size depends on local nest survival rate in a mean of bet-hedging in a shorebird. Avian Res. 11, 40.
    Song, Z., Que, P., Jones, W., Huang, C., Halimubieke, N., Ding, P., et al., 2023. Colder Ambient Temperatures Constrain Female Mate Preference for Ornamental Traits. Authorea.
    Sozcu, A., Ipek, A., 2015. Acute and chronic eggshell temperature manipulations during hatching term influence hatchability, broiler performance, and ascites incidence. Poultry Sci. 94, 319–327.
    Sözcü, A., İpek, A., van den Brand, H., 2022. Eggshell temperature during early and late incubation affects embryo and hatchling development in broiler chicks. Poultry Sci. 101, 102054.
    Stearns, S.C., 1989. Trade-offs in life-history evolution. Funct. Ecol. 3, 259.
    Stefanello, C., Santos, T.C., Murakami, A.E., Martins, E.N., Carneiro, T.C., 2014. Productive performance, eggshell quality, and eggshell ultrastructure of laying hens fed diets supplemented with organic trace minerals. Poultry Sci. 93, 104–113.
    Stoddard, M.C., Yong, E.H., Akkaynak, D., Sheard, C., Tobias, J.A., Mahadevan, L., 2017. Avian egg shape: Form, function, and evolution. Science 356, 1249–1254.
    Stoewsand, G.S., Anderson, J.L., Gutenmann, W.H., Lisk, D.J., 1978. Influence of dietary calcium selenium and methylmercury on eggshell thickness in Japanese quail. Bull. Environ. Contam. Toxicol. 20, 135–142.
    Stoffel, M.A., Nakagawa, S., Schielzeth, H., 2017. rptR: repeatability estimation and variance decomposition by generalized linear mixed-effects models. Methods Ecol. Evol. 8, 1639–1644.
    Székely, T., Kosztolányi, A., Küpper, C., 2008. Practical Guide for Investigating Breeding Ecology of Kentish Plover Charadrius Alexandrinus. Unpublished Report, University of Bath. .
    van der Pol, C.W., van Roovert-Reijrink, I.A.M., Maatjens, C.M., van den Brand, H., Molenaar, R., 2013. Effect of relative humidity during incubation at a set eggshell temperature and brooding temperature posthatch on embryonic mortality and chick quality. Poultry Sci. 92, 2145–2155.
    Vincze, O., Székely, T., Küpper, C., Alrashidi, M., Amat, J.A., Ticó, A.A., et al., 2013. Local environment but not genetic differentiation influences biparental care in ten plover populations. PLoS One 8, e60998.
    Wang, P., Cao, J.-J., Wu, F., 2010. Environmental background values and its impact factors of topsoil within the Lake Qinghai catchment, Northeast Tibetan Plateau, China. J. Earth Environ. 3, 189–200.
    Wang, X., Que, P., Heckel, G., Hu, J., Zhang, X., Chiang, C.Y., et al., 2019. Genetic, phenotypic and ecological differentiation suggests incipient speciation in two Charadrius plovers along the Chinese coast. BMC Evol. Biol. 19, 1–18.
    Xin, Q., Wang, M., Jiao, H., Zhao, J., Li, H., Wang, X., et al., 2021. Prolonged scotophase within a 24 hour light regime improves eggshell quality by enhancing calcium deposition in laying hens. Poultry Sci. 100, 101098.
    Yang, C., Huang, Q., Wang, L., Du, W.-G., Liang, W., Møller, A.P., 2018. Keeping eggs warm: thermal and developmental advantages for parasitic cuckoos of laying unusually thick-shelled eggs. Naturwissenschaften 105, 10.
    Zhang, Y.N., Zhang, H.J., Wu, S.G., Wang, J., Qi, G.H., 2017. Dietary manganese supplementation modulated mechanical and ultrastructural changes during eggshell formation in laying hens. Poultry Sci. 96, 2699–2707.
  • Related Articles

Catalog

    Figures(3)  /  Tables(4)

    Article Metrics

    Article views (22) PDF downloads (17) Cited by()

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return