温度和营养盐对微型裸腹溞生活史的影响
The Effects of Temperature and Nutrient Salts on the Life History of Moina micrura
DOI: 10.12677/aep.2025.156101, PDF,   
作者: 杨润东:温州大学生命与环境科学学院,浙江 温州
关键词: 温度营养盐微型裸腹溞生活史Temperature Nutrient Salts Moina micrura Life History
摘要: 在全球气候变化和水体富营养化日益加剧的背景下,温度升高与氮营养盐浓度变化已成为影响水生生态系统结构和功能的关键环境因子。作为水生生态系统的关键消费者,浮游动物的生活史特征对环境变化的响应机制是理解生态系统能量流动和物质循环的重要基础。本论文选取微型裸腹溞(Moina micrura)为实验对象开展室内试验,设置不同氮营养盐浓度梯度(0.112, 0.224, 1.12, 2.24, 11.2 mg/L),探究了不同氮营养盐条件下浮游动物对小球藻的摄食关系;随后基于摄食关系实验选取0.224 mg/L和2.24 mg/L两个氮营养盐浓度及25℃和30℃两个温度梯度进行实验。通过对微型裸腹溞生活史进行研究,结果表明,在25℃~30℃范围内,温度升高显著加快微型裸腹溞的代谢速度,使其内禀增长率和净生殖率提升,繁殖时间与世代周期缩短,种群增长加快;而氮浓度升高能提高种群生物量,促进初期增殖,且使后代个体更大。研究揭示了温度与氮营养盐相互作用对微型裸腹溞生活史的复杂影响机制,即温度主要通过加速代谢过程影响繁殖效率,氮营养盐则从直接参与生理代谢和间接优化食物质量两方面发挥作用。
Abstract: In the face of intensifying global climate change and increasing aquatic eutrophication, elevated temperatures and altered nitrogen nutrient salt concentrations have become pivotal environmental factors affecting the structure and functioning of aquatic ecosystems. As keystone consumers in aquatic ecosystems, the response mechanism of zooplankton’s life history traits to environmental changes is an important basis for understanding the energy transfer and material cycling of ecosystems. This study selected Moina micrura as an experimental subject to conduct indoor experiments and set up different nitrogen nutrient salt concentration gradients (0.112, 0.224, 1.12, 2.24, and 11.2 mg/L) to study zooplankton-algal feeding relations under the conditions of different nitrogen nutrient salts. Then, it selected two nitrogen nutrient salt concentrations of 0.224 mg/L and 2.24 mg/L and two temperature gradients of 25˚C and 30˚C for further experiments based on the feeding relationship experiment. Through the study of the life history of Moina micrura, the results showed that at 25˚C~30˚C, higher temperatures sped up the metabolism of Moina micrura, increasing its intrinsic growth and net reproductive rates and shortening reproduction time and generation length, thus accelerating population growth. Higher nitrogen nutrient salt concentrations also increased the population biomass, enhanced initial reproduction, and produced larger offspring. The study revealed the complex interplay of temperature and nitrogen nutrient salt on the life history of Moina micrura. Temperature mainly affected reproduction efficiency by raising metabolic rates, while nitrogen nutrient salts influenced physiological metabolism directly and food quality optimization indirectly.
文章引用:杨润东. 温度和营养盐对微型裸腹溞生活史的影响[J]. 环境保护前沿, 2025, 15(6): 900-908. https://doi.org/10.12677/aep.2025.156101

参考文献

[1] Karmakar, S.R., Hossain, M.B., Sarker, M.M., Nur, A.U., Habib, A., Paray, B.A., et al. (2022) Diversity and Community Structure of Zooplankton in Homestead Ponds of a Tropical Coastal Area. Diversity, 14, Article No. 755. [Google Scholar] [CrossRef
[2] Ger, K.A., Urrutia-Cordero, P., Frost, P.C., Hansson, L., Sarnelle, O., Wilson, A.E., et al. (2016) The Interaction between Cyanobacteria and Zooplankton in a More Eutrophic World. Harmful Algae, 54, 128-144. [Google Scholar] [CrossRef] [PubMed]
[3] Sotton, B., Guillard, J., Anneville, O., Maréchal, M., Savichtcheva, O. and Domaizon, I. (2014) Trophic Transfer of Microcystins through the Lake Pelagic Food Web: Evidence for the Role of Zooplankton as a Vector in Fish Contamination. Science of the Total Environment, 466, 152-163. [Google Scholar] [CrossRef] [PubMed]
[4] Xiong, W., Ni, P., Chen, Y., Gao, Y., Li, S. and Zhan, A. (2019) Biological Consequences of Environmental Pollution in Running Water Ecosystems: A Case Study in Zooplankton. Environmental Pollution, 252, 1483-1490. [Google Scholar] [CrossRef] [PubMed]
[5] Heneghan, R.F., Everett, J.D., Blanchard, J.L., Sykes, P. and Richardson, A.J. (2023) Climate-Driven Zooplankton Shifts Cause Large-Scale Declines in Food Quality for Fish. Nature Climate Change, 13, 470-477. [Google Scholar] [CrossRef
[6] Tao, T., Wang, H., Na, X., Liu, Y., Zhang, N., Lu, X., et al. (2023) Temperate Urban Wetland Plankton Community Stability Driven by Environmental Variables, Biodiversity, and Resource Use Efficiency: A Case of Hulanhe Wetland. Frontiers in Ecology and Evolution, 11, Article 1148580. [Google Scholar] [CrossRef
[7] 吴明姝. 安徽省太平湖水库浮游动物群落结构及水质评价[D]: [硕士学位论文]. 上海: 上海师范大学, 2015.
[8] Huntley, M.E. (1992) Temperature-Dependent Production of Marine Copepods: A Global Synthesis. The American Naturalist, 140, 201-242. [Google Scholar] [CrossRef] [PubMed]
[9] Sarma, S.S.S., Nandini, S. and Gulati, R.D. (2005) Life History Strategies of Cladocerans: Comparisons of Tropical and Temperate Taxa. Hydrobiologia, 542, 315-333. [Google Scholar] [CrossRef
[10] Sokolova, I. (2021) Bioenergetics in Environmental Adaptation and Stress Tolerance of Aquatic Ectotherms: Linking Physiology and Ecology in a Multi-Stressor Landscape. Journal of Experimental Biology, 224, jeb236802. [Google Scholar] [CrossRef] [PubMed]
[11] Zhao, Q., Liu, S. and Niu, X. (2020) Effect of Water Temperature on the Dynamic Behavior of Phytoplankton-Zooplankton Model. Applied Mathematics and Computation, 378, Article ID: 125211. [Google Scholar] [CrossRef
[12] Elser, J.J., Fagan, W.F., Denno, R.F., Dobberfuhl, D.R., Folarin, A., Huberty, A., et al. (2000) Nutritional Constraints in Terrestrial and Freshwater Food Webs. Nature, 408, 578-580. [Google Scholar] [CrossRef] [PubMed]
[13] Auer, B., et al. (2004) Comparison of Pelagic Food Webs in Lakes along a Trophic Gradient and with Seasonal Aspects: Influence of Resource and Predation. Journal of Plankton Research, 26, 697-709. [Google Scholar] [CrossRef
[14] Moody, E.K. and Wilkinson, G.M. (2019) Functional Shifts in Lake Zooplankton Communities with Hypereutrophication. Freshwater Biology, 64, 608-616. [Google Scholar] [CrossRef
[15] Vehmaa, A., Katajisto, T. and Candolin, U. (2018) Long‐Term Changes in a Zooplankton Community Revealed by the Sediment Archive. Limnology and Oceanography, 63, 2126-2139. [Google Scholar] [CrossRef
[16] Moore, M. and Folt, C. (1993) Zooplankton Body Size and Community Structure: Effects of Thermal and Toxicant Stress. Trends in Ecology & Evolution, 8, 178-183. [Google Scholar] [CrossRef] [PubMed]
[17] Bruijning, M., ten Berge, A.C.M. and Jongejans, E. (2018) Population‐Level Responses to Temperature, Density and Clonal Differences in daphnia Magna as Revealed by Integral Projection Modelling. Functional Ecology, 32, 2407-2422. [Google Scholar] [CrossRef
[18] Pineda-Mendoza, R.M., Zúñiga, G. and Martínez-Jerónimo, F. (2014) Infochemicals Released by Daphnia Magna Fed on Microcystis Aeruginosa Affect Mcya Gene Expression. Toxicon, 80, 78-86. [Google Scholar] [CrossRef] [PubMed]
[19] Brooks, J.L. and Dodson, S.I. (1965) Predation, Body Size, and Composition of Plankton. Science, 150, 28-35. [Google Scholar] [CrossRef] [PubMed]
[20] Morgan, C.A., Cordell, J.R. and Simenstad, C.A. (1997) Sink or Swim? Copepod Population Maintenance in the Columbia River Estuarine Turbidity-Maxima Region. Marine Biology, 129, 309-317. [Google Scholar] [CrossRef
[21] Wagner, N.D., Hillebrand, H., Wacker, A. and Frost, P.C. (2013) Nutritional Indicators and Their Uses in Ecology. Ecology Letters, 16, 535-544. [Google Scholar] [CrossRef] [PubMed]
[22] Sterner, R.W. (1993) Daphnia Growth on Varying Quality of Scenedesmus: Mineral Limitation of Zooplankton. Ecology, 74, 2351-2360. [Google Scholar] [CrossRef
[23] Frost, P.C., Evans‐White, M.A., Finkel, Z.V., Jensen, T.C. and Matzek, V. (2005) Are You What You Eat? Physiological Constraints on Organismal Stoichiometry in an Elementally Imbalanced World. Oikos, 109, 18-28. [Google Scholar] [CrossRef