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Experimental Study of Population Variations on the Morphology and Reproduction of Daphnia galeata from Three Chinese Lakes

Received: 24 July 2021    Accepted: 11 August 2021    Published: 26 August 2021
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Abstract

Environmental heterogeneity affected the genetic differentiation and phenotypic plasticity of Daphnia spp. populations in different lakes. However, the effect mechanism of lake population on the morphology and reproduction of Daphnia spp. was still unclear. This paper studied the differences of the morphology and reproduction of D. galeata populations from three Chinese lakes (CH: Lake Chaohu, NH: Lake Nanhu, EH: Lake Erhai), which the area size, nutrient levels, phytoplankton biomass and dominant fish were obviously various in the three lakes. The results showed that lake population affected significantly the morphology (helmet length and tail spine length) and reproduction (no. offspring at first reproduction per female-1) of D. galeata. Both helmet lengths and tail spine lengths of three D. galeata populations increased quickly within the first five instars, and afterwards showed various patterns. Multiple comparisons indicated that helmet lengths of NH population were significantly higher than those in EH and CH populations (P<0.001) whereas tail spine lengths of NH population were significantly smaller than those in EH (P=0.001) and CH (P=0.003) populations. The ratio of relative helmet length of CH population was significantly shorter than those of EH population (P<0.001) and NH population (P<0.001), and the ratio of relative tail spine length at first pregnancy of EH population was significantly longer than those of CH population (P<0.001) and NH population (P<0.001). Moreover, there is four juvenile instars in EH population whereas there are three juvenile instars in CH and NH populations. With the increase of adult instars, the number of offspring produced by D. galeata in all three populations displayed a similar pattern, which increased quickly at first, and then gradually decreased. Average maximum number of offspring at first reproduction (6.3±1.4 ind. per female-1) appeared in CH population, followed by EH (5.2±1.7 ind. per female-1) and NH (4.9±1.4 ind.•per female-1) populations. The innate rate of increase of CH population was relatively higher than those of EH and NH populations, but no significant differences among three populations were observed. Our results suggested that environmental heterogeneity could affect the reproduction and morphological plasticity of Daphnia spp. in different lakes.

Published in American Journal of Environmental Science and Engineering (Volume 5, Issue 3)
DOI 10.11648/j.ajese.20210503.12
Page(s) 63-69
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Daphnia galeata, Morphology, Reproduction, Population, Phenotypic Plasticity

References
[1] Benzie, J. A. H. (2005). The genus Daphnia (including Daphniopsis) (Anomopoda: Daphniidae) (In: [Dumont HJF] Ed: Guides to the identification of the microinvertebrates of the continental waters of the world 21) ─ Leiden, Backhuys Publishers, 172-176.
[2] Hartwich, M., Martin-Creuzburg, D., Rothhaupt, K. O., & Wacker, A. (2012). Oligotrophication of a large, deep lake alters food quantity and quality constraints at the primary producer-consumer interface. Oikos, 121 (10), 1702-1712.
[3] Cui, R. X., Kwak, J. Il, & An Y. J. (2018). Comparative study of the sensitivity of Daphnia galeata and Daphnia magna to heavy metals. Ecotoxicology and Environmental Safety, 162 (1), 63-70.
[4] Liu, Q., Deng, D. G., Zhang, K., He, P., Sun, Y. C., Zhang, T. T., Yang, W., & Liu, W. (2019). Genetic diversity and differentiation of Daphnia galeata in the middle and lower reaches of the Yangtze River, China. Ecology and Evolution, 9 (22), 12688-12700.
[5] Zuykova, E. I., & Bochkarev, N. A. (2011). Population morphological variability of the Daphnia galeata populations (Cladocera: Anomopoda) in the lakes of the Todzha depression. Russian Journal of Ecology, 42 (4), 296-304.
[6] Ma, X., Wolinska, J., Petrusek, A., Gieẞler, S., Hu, W., & Yin, M. (2019). The phenotypic plasticity in Chinese populations of Daphnia similoides sinensis: recurvate helmeted forms are associated with the presence of predators. Journal of Plankton Research, 38 (4), 855-864.
[7] Sommer, U., Gliwicz, Z. M., Lampert, W., & Duncan, A. (1986). The PEG model of seasonal succession of planktonic events in fresh waters. Archiv für Hydrobiologie, 106 (4), 433-471.
[8] Deng, D. G., Xie, P., Zhou, Q., Yang, H., Guo, L. G., & Geng, H. (2008). Field and experimental studies on the combined impacts of cyanobacterial blooms and small algae on crustacean zooplankton in a large, eutrophic subtropical Chinese lake. Limnology, 9 (1), 1-11.
[9] Prater, C., Wagner, N. D., & Frost P. C. (2017). Interactive effects of genotype and food quality on consumer growth rate and elemental content. Ecology, 98 (5), 1399-1408.
[10] Ming, R. L., Liu, R. Q., & Lin, Q. Q. (2019). Effect of food quality (C: P ratio) and interspecific competition on population growth of Daphnia galeata and Bosmina fatalis. Journal of Lake Sciences, 31 (1), 211-219 (in Chinese).
[11] Elser, J. J., Bracken, M. E. S., Cleland, E. E., Gruner, D. S., Harpole, W. S., Hillebrand, H., Ngai, J. T., Seabloom, E. W., Shurin, J. B., & Smith, J. E. (2007). Global analysis of nitrogen and phosphorus limitation of primary producers in freshwater, marine and terrestrial ecosystems. Ecology Letters, 10 (12), 1135─1142.
[12] Weers, P. M. M., & Gulati, R. D. (1997). Growth and reproduction of Daphnia galeata in response to changes in fatty acids, phosphorus, and nitrogen in Chlamydomonas reinhardtii. Limnology and Oceanography, 42 (7), 1584 -1589.
[13] Meng, M. R., Deng, D. G., Zhang, X. L., Ge, Q., & Zhang, K. (2014). The influence of different phosphorus concentrations on the population dynamics and resting egg formation of two cladocerans. Journal of Freshwater Ecology, 29 (3), 387-396.
[14] Deng, D. G., Meng, Q., Yin, S. T., Feng, N. S., & Xiao, Q. Q. (2008). Effect of temperature and food concentration on population dynamic and sexual reproduction of Daphnia magna. Acta Ecologica Sinica, 28 (9), 4268-4276 (in Chinese).
[15] Ma, X., Petrusek, A., Wolinska, J., Giebler, S., Zhong, Y., Yang, Z., Hu, W., & Yin, M. (2015). Diversity of the Daphnia longispina species complex in Chinese lakes: A DNA taxonomy approach. Journal of Plankton Research. 37 (1), 56-65.
[16] Ma, X., Hu, W., Smilauer, P., Yin, M., & Wolinska, J. (2019). Daphnia galeata and D. dentifera are geographically and ecologically separated whereas their hybrids occur in intermediate habitats: a survey of 44 Chinese lakes. Molecular Ecology, 28 (4), 785-802.
[17] Yang, W., Deng, D. G., Zhang, S., & Hu, C. L. (2014). Seasonal dynamics of community structure of crustacean zooplankton in Erhai Lake, a plateau lake, with reference to phytoplankton and environmental factors. Chinese Journal of Oceanology and Limnology, 32 (5), 1074-1082.
[18] He, P., Zhang, K., Deng, D. G., Liu, Q., Guo, H. H., Zhang, T. T., & Sun Y. C. (2018). Vertical distribution of Daphnia ephippia and its correlation with total nitrogen and total phosphorus in the sediments of Meiliang Bay in Lake Taihu. Chinese Journal of Ecology, 37 (8), 2411-2417 (in Chinese).
[19] Liu, Q., H, e P., Peng, S. X., Zhang, T. T., Sun, Y. C., & Deng D. G. (2018). Long-term changes of ephippial densities of Daphnia species in the sediment of isolated lakes of Poyang Lake - Junshan Lake and its correlation with the nutrients. Journal of Lake Science, 30 (5), 1388-1399 (in Chinese).
[20] Zhang, K., Deng, D. G., Wang, W. P., Peng, S. X., Liu, F., & Ji, L. (2020). Long-term eutrophication affects vertical changes of Daphnia ephippia in the sediments of a subtropical Chinese lake. Evironmental Science and Pollution Research. 27 (5), 4737-4745.
[21] Boersma, M., Spaak, P., & De Meester, L. (1998). Predator-mediated plasticity in morphology, life history, and behavior of Daphnia: the uncoupling of responses. The American Naturalist, 152 (2), 237-248.
[22] Tolardo, M., da, Silva, Ferrão-Filho, A., & Santagelo, J. M. (2016). Species and clone-dependent effects of tilapia fish (Cichlidae) on the morphology and life-history of temperate and tropical Daphnia. Ecological Research, 31 (3), 333-342.
[23] Tams, V., Lüneburg, J., Seddar, L., Detampel, J. P., & Cordellier, M. (2018). Intraspecific phenotypic variation in life history traits of Daphnia galeata populations in response to fish kairomones. Peer J, 6, e5746.
[24] Spitze, K. (1992). Predator-mediated plasticity of prey life history and morphology: Chaoborus americanus predation on Daphnia pulex. The American Naturalist, 139 (2), 229-247.
[25] Weider, L. J., & Hebert P. D. N. (1987). Ecological and physiological differentiation among low-arctic clones of Daphnia pulex. Ecology, 68 (1), 188-198.
[26] Antunes, S. C., Castro, B. B, & Gonçalves, F. (2003). Chronic responses of different clones of Daphnia longispina (field and ephippia) to different food levels. Acta Oecologica, 24 (1), 325-332.
[27] Davidson, A. M., Jennions, M., Nicotra, A. B. (2011). Do invasive species show higher phenotypic plasticity than native species and, if so, is it adaptive? A meta-analysis. Ecology Letters, 14 (4), 419-431.
[28] Wang, W. P., Zhang, K., Deng, D. G., Zhang, Y. N., Peng, S. X., & Xu, X. X. (2016). Genetic diversity of Daphnia pulex in the middle and lower reaches of the Yangtze River. Plos One, 11, e0152436.
[29] Tokishita, S., Shibuya, H., Kobyashi, T., Sakamoto, M., Ha, J. Y., Yokobori, S., Yamagata, H., & Hanazato, T. (2017). Diversification of mitochondrial genome of Daphnia galeata (Cladocera, Crustacea): comparison with phylogenetic consideration of the complete sequences of clones isolated from five lakes in Japan. Gene, 611, 38-46.
[30] Wu, J. X., Wang, W. P., Deng, D. G., Zhang, K., Peng, S. X., Xu, X. X., Zhang, Y. N., & Zhou, Z. Z. (2019). Genetic diversity and phylogeography of Daphnia similoides sinensis located in the middle and lower reaches of the Yangtze River. Ecology and Evolution, 9 (8), 4362-4372.
[31] Wu, J. X., Zhang, K., Deng, D. G., Liu, Q., Peng, S. X., Zhang, T. T., & Zhou, Z. Z. (2019). Effects of rapid enclosure of aquatic ecosystems on genetic diversity and genetic structure of Daphnia similoides sinensis in a eutrophic Chinese lake. Russian Journal of Ecology, 50 (3), 289-299.
[32] Stoks, R., Govaert, L., Pauwels, K., Jansen, B., & De, Meester, L. (2016). Resurrecting complexity: the interplay of plasticity and rapid evolution in the multiple trait response to strong changes in predation pressure in the water flea Daphnia magna. Ecology Letters, 19 (2), 180-190.
[33] Harney, E., Paterson, S., & Plaistow, S. J. (2017). Offspring development and life-history variation in a water flea depends upon clone-specific integration of genetic, non-genetic and environmental cues. Functional Ecology, 31 (10), 1996-2007.
[34] Huang, C., Liu, Q. G., Hu, Z. J., Hou, W. H., Wu, J. Y., He, G. X., & Chen, L. S. (2014). Effects of different algae as food on growth of water fleas Daphnia hyalina. Journal of Dalian Ocean University. 29 (2), 131-135 (in Chinese).
[35] Huang, X. F., Zhang, X. L., Franja, P., & Han, B. P. (2017). Growth and reproduction of two Daphnia species (D. sinensis and D. galeata) in tropics at five levels of food concentrations. Chinese Journal of Applied and Environmental Biology, 23 (6), 1148-1153 (in Chinese).
[36] Yang, W., Deng, D. G., Meng, X. L., & Zhang, S. (2019) Temporal and spatial variations of phytoplankton community structure in Lake Erhai, a Chinese plateau lake, with reference to environmental factors. Russian Journal of Ecology, 50 (4), 352-360.
[37] Deng, D. G., Xing, R. L., Ma, R., Zhang, S., Meng, X. L., & Yang, W. (2010). Seasonal variations on community structure of crustacean zooplankton in a small lake of an excavating coal subsidence region in Huaibei City. Journal of Lake Sciences, 22 (4), 591-597 (in Chinese).
[38] Hendry, A. P., Farrugia, T. J., & Kinnison, M. T. (2008). Human influences on rates of phenotypic change in wild animal populations. Molecular Ecology, 17 (1), 20-29.
[39] Gustafsson, S., Rengefors, K., Hansson, L. A. (2005). Increased consumer fitness following transfer of toxin tolerance to offspring via maternal effects. Ecology, 86 (10), 2561-2567.
[40] Walsh, M. R., Castoe, T., Holmes, J., Packer, M., Biles, K., Walsh, M., Munch, S. B., & Post, D. M. (2016). Local adaptation in transgenerational responses to predators. Proceedings of the Royal Society B: Biological Sciences, 283 (1823), 20152271.
[41] Radersma, R., Hegg, A., Noble, D. W. A., & Uller, T. (2018). Timing of maternal exposure to toxic cyanobacteria and offspring fitness in Daphnia magna: implications for the evolution of anticipatory maternal effects. Ecology and Evolution, 8 (24), 12727-12736.
[42] Rinke, K., Hülsmann, S., & Mooij, W. M. (2008). Energetic costs, underlying resource allocation patterns, and adaptive value of predator-induced life-history shifts. Oikos, 117 (2), 273-285.
[43] Larsson, P., & Dodson, S. I. (1993). Invited review: chemical communication in planktonic animals. Archiv fur Hydrobiologie, 129 (2), 129-155.
[44] Ke, Z., & Huang, L. (2009). Advance in the study on the anti-predator phenotypic plasticity of Daphnia. Journal of Lake Sciences, 21 (6), 758-767 (in Chinese).
[45] Alexander, T. J., Vonlanthen, P., & Seehausen, O. (2017). Does eutrophication-driven evolution change aquatic ecosystems? Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 372 (1712), 20160041.
[46] Weber, A., & Vesela, S. (2002). Optimising survival under predation: chemical cues modify curvature in Daphnia galeata. Aquatic Ecology, 36 (4), 519-527.
[47] Huang, X. (1984). Effect of temperature on development and growth of Daphnia hyalina and Daphnia carinata ssp. (Cladocera: Daphniadae). Acta Hydrobiologica Sinica, 8 (2), 207-224 (in Chinese).
[48] Repka, S. (1997). Effects of food type on the life history of Daphnia clones from lakes differing in trophic state. Freshwater biology, 38 (3), 675-683.
Cite This Article
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    Yaqin Cao, Huiying Qi, Jun Li, Kun Zhang, Daogui Deng. (2021). Experimental Study of Population Variations on the Morphology and Reproduction of Daphnia galeata from Three Chinese Lakes. American Journal of Environmental Science and Engineering, 5(3), 63-69. https://doi.org/10.11648/j.ajese.20210503.12

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    Yaqin Cao; Huiying Qi; Jun Li; Kun Zhang; Daogui Deng. Experimental Study of Population Variations on the Morphology and Reproduction of Daphnia galeata from Three Chinese Lakes. Am. J. Environ. Sci. Eng. 2021, 5(3), 63-69. doi: 10.11648/j.ajese.20210503.12

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    AMA Style

    Yaqin Cao, Huiying Qi, Jun Li, Kun Zhang, Daogui Deng. Experimental Study of Population Variations on the Morphology and Reproduction of Daphnia galeata from Three Chinese Lakes. Am J Environ Sci Eng. 2021;5(3):63-69. doi: 10.11648/j.ajese.20210503.12

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  • @article{10.11648/j.ajese.20210503.12,
      author = {Yaqin Cao and Huiying Qi and Jun Li and Kun Zhang and Daogui Deng},
      title = {Experimental Study of Population Variations on the Morphology and Reproduction of Daphnia galeata from Three Chinese Lakes},
      journal = {American Journal of Environmental Science and Engineering},
      volume = {5},
      number = {3},
      pages = {63-69},
      doi = {10.11648/j.ajese.20210503.12},
      url = {https://doi.org/10.11648/j.ajese.20210503.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajese.20210503.12},
      abstract = {Environmental heterogeneity affected the genetic differentiation and phenotypic plasticity of Daphnia spp. populations in different lakes. However, the effect mechanism of lake population on the morphology and reproduction of Daphnia spp. was still unclear. This paper studied the differences of the morphology and reproduction of D. galeata populations from three Chinese lakes (CH: Lake Chaohu, NH: Lake Nanhu, EH: Lake Erhai), which the area size, nutrient levels, phytoplankton biomass and dominant fish were obviously various in the three lakes. The results showed that lake population affected significantly the morphology (helmet length and tail spine length) and reproduction (no. offspring at first reproduction per female-1) of D. galeata. Both helmet lengths and tail spine lengths of three D. galeata populations increased quickly within the first five instars, and afterwards showed various patterns. Multiple comparisons indicated that helmet lengths of NH population were significantly higher than those in EH and CH populations (PP=0.001) and CH (P=0.003) populations. The ratio of relative helmet length of CH population was significantly shorter than those of EH population (PPPPD. galeata in all three populations displayed a similar pattern, which increased quickly at first, and then gradually decreased. Average maximum number of offspring at first reproduction (6.3±1.4 ind. per female-1) appeared in CH population, followed by EH (5.2±1.7 ind. per female-1) and NH (4.9±1.4 ind.•per female-1) populations. The innate rate of increase of CH population was relatively higher than those of EH and NH populations, but no significant differences among three populations were observed. Our results suggested that environmental heterogeneity could affect the reproduction and morphological plasticity of Daphnia spp. in different lakes.},
     year = {2021}
    }
    

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  • TY  - JOUR
    T1  - Experimental Study of Population Variations on the Morphology and Reproduction of Daphnia galeata from Three Chinese Lakes
    AU  - Yaqin Cao
    AU  - Huiying Qi
    AU  - Jun Li
    AU  - Kun Zhang
    AU  - Daogui Deng
    Y1  - 2021/08/26
    PY  - 2021
    N1  - https://doi.org/10.11648/j.ajese.20210503.12
    DO  - 10.11648/j.ajese.20210503.12
    T2  - American Journal of Environmental Science and Engineering
    JF  - American Journal of Environmental Science and Engineering
    JO  - American Journal of Environmental Science and Engineering
    SP  - 63
    EP  - 69
    PB  - Science Publishing Group
    SN  - 2578-7993
    UR  - https://doi.org/10.11648/j.ajese.20210503.12
    AB  - Environmental heterogeneity affected the genetic differentiation and phenotypic plasticity of Daphnia spp. populations in different lakes. However, the effect mechanism of lake population on the morphology and reproduction of Daphnia spp. was still unclear. This paper studied the differences of the morphology and reproduction of D. galeata populations from three Chinese lakes (CH: Lake Chaohu, NH: Lake Nanhu, EH: Lake Erhai), which the area size, nutrient levels, phytoplankton biomass and dominant fish were obviously various in the three lakes. The results showed that lake population affected significantly the morphology (helmet length and tail spine length) and reproduction (no. offspring at first reproduction per female-1) of D. galeata. Both helmet lengths and tail spine lengths of three D. galeata populations increased quickly within the first five instars, and afterwards showed various patterns. Multiple comparisons indicated that helmet lengths of NH population were significantly higher than those in EH and CH populations (PP=0.001) and CH (P=0.003) populations. The ratio of relative helmet length of CH population was significantly shorter than those of EH population (PPPPD. galeata in all three populations displayed a similar pattern, which increased quickly at first, and then gradually decreased. Average maximum number of offspring at first reproduction (6.3±1.4 ind. per female-1) appeared in CH population, followed by EH (5.2±1.7 ind. per female-1) and NH (4.9±1.4 ind.•per female-1) populations. The innate rate of increase of CH population was relatively higher than those of EH and NH populations, but no significant differences among three populations were observed. Our results suggested that environmental heterogeneity could affect the reproduction and morphological plasticity of Daphnia spp. in different lakes.
    VL  - 5
    IS  - 3
    ER  - 

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Author Information
  • School of Life Science, Huaibei Normal University, Huaibei, China

  • School of Life Science, Huaibei Normal University, Huaibei, China

  • School of Life Science, Huaibei Normal University, Huaibei, China

  • School of Life Science, Huaibei Normal University, Huaibei, China

  • School of Life Science, Huaibei Normal University, Huaibei, China

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