Effects of rifampicin on life table demography of Brachionus calyciflorus under different Scenedesmus obliquus densities
ZHAI Pan, WEN Xin-li, CHEN Zhi-wen, ZHAO Zheng, LI Hai-yang, XI Yi-long
Center of Cooperative Innovation for Recovery and Reconstruction of Degraded Ecosystem in Wanjiang City Belt, Provincial Key Laboratory of Biotic Environment and Ecological Safety in Anhui, College of Life Sciences, Anhui Normal University, Wuhu 241000, China
By means of life-table technique, the effects of rifampicin at 2.0, 4.0, 6.0, 8.0, and 10.0μg/mL on the population growth parameters of Brachionuscalyciflorus under three Scenedesmus obliquus densities (1.0×106, 2.0×106and 4.0×106cells/mL) were studied. The results showed that compared to the controls, rifampicin at all the test concentrations obviously promoted the proportion of sexual offspring under the algal density of 1.0×106cells/mL (P < 0.05). When algal density was 2.0×106cells/mL, rifampicin at 2.0, 4.0 and 10.0μg/mL increased the intrinsic rate of population increase (P < 0.05), and rifampicin at all the test concentrations also increased the proportion of sexual offspring. When algal density was 4.0×106cells/mL, rifampicin at all the test concentrations obviously promoted the intrinsic rate of population increase and the proportion of sexual offspring (P < 0.05). There were significant dose-effect relationships between rifampicin concentration and the life expectancy at hatching, the generation time, the average lifespan, and the average lifespan of the rotifers fed on the 1.0×106cells/mL of algae. When algae density was 2.0×106cells/mL, there were significant dose-effect relationships between the concentration of rifampicin and the proportion of sexual offspring. When algal density was 4.0×106cells/mL, there were significant dose-effect relationships between the rifampicin concentration and the generation time, the net reproductive rate, the intrinsic rate of population increase as well as the proportion of sexual offspring.
翟盼, 温新利, 陈治文, 赵政, 李海洋, 席贻龙. 抗生素利福平对萼花臂尾轮虫生命表参数的影响[J]. 中国环境科学, 2016, 36(6): 1886-1894.
ZHAI Pan, WEN Xin-li, CHEN Zhi-wen, ZHAO Zheng, LI Hai-yang, XI Yi-long. Effects of rifampicin on life table demography of Brachionus calyciflorus under different Scenedesmus obliquus densities. CHINA ENVIRONMENTAL SCIENCECE, 2016, 36(6): 1886-1894.
Wallance R L, Snell T W. Rotifera: Ecology and systematic of North American freshwater invertebrates [M]. New York: Acadamic Press. 1991.
[11]
Araujo A, McNair J. Individual-and population-level effects of antibiotics on the rotifers, Brachionus calyciflorus and B.plicatilis [J]. Hydrobiologia, 2007,593(1):185-199.
Li Y Y, Floate K D, Fields P G, et al. Review of treatment methods to remove Wolbachia bacteria from Arthopods [J]. Symbiosis, 2014,62(1):1-15.
[17]
Werren J H, Loehlin D W. Curing Wolbachia Infections in Nasonia (Parasitoid Wasp) [EB/OL]. Cold Spring Harbor Protocols, 2009(10):pdb.prot5312. doi:10.1101/pdb.prot5312.
[18]
Grenier S, Gomes S M, Pintureau B, et al. Use of tetracycline in larval diet to study the effect of Wolbachia on host fecundity and clarify taxonomic status of Trichogramma species in cured bisexual lines [J]. Journal of Invertebrate Pathology, 2002,80(1): 13-21.
[19]
Konkou K, Pavlikaki H, Kilias G, et al. Influence of antibiotic treatment and Wolbachia curing on sexual isolation among Drosophila melanogaster cage populations [J]. Evolution, 2006,60(1):87-96.
US EPA. Methods for measuring the acute toxicity of effluents to freshwater and marine organisms [S]. Peltier WH, Weber CI ed. EPA/600/4-85/013. Washington DC: US Environ. Protec. Agency, 1985.
Huang L, Xi Y L, Zha C W. Effect of aldrin on life history characteristics of rotifer Brachionus calyciflorus Pallas [J]. Bulletin of Environmental Contamination and Toxicology, 2007,79(1):524-528.
Isidori M, Lavorgna M, Nardelli A, et al. Toxic and genotoxic evaluation of six antibiotics on non-target organisms [J]. Science of the Total Environment, 2005,346(1-3):87-98.
[30]
Gianluigi D D, Agostino M, Cinzia C, et al. Antibiotics of zootechnical use: Effects of acute high and low dose contamination on Daphnia magna Straus [J]. Aquatic Toxicology, 1992,22(1):53-59.
[31]
Sarma S S S, Nandini S, Gama Flores J L. Effect of methyl parathion on the population growth of the Rotifer Brachionus patulus (O. F. Müller) under different algal food (Chlorella vulgaris) densities [J]. Ecotoxicology and Environmental Safety, 2001,48(2):190-195.
[32]
Gama-Flpres J L, Sarma S, Nandini S. Acute and chronic toxicity of the pesticide methyl parathion to the rptifer Brachionus angularis (Rotifera) at differentalgal (Chlorella vulgaris) food densities [J]. Aquatic Ecology, 2004,38(1):27-36.
[33]
Peredo-Álvarez M V, Sarma S S S, Nandini S. Combined effect of concentrations of algal food (Chlorella vulgaris) and salt (sodium chloride) on the population growth of Brachionus calyciflorus and Brachionus patulus (Rotifera) [J]. Revista de Biología Tropical, 2003,51(2):154-160.
[34]
Mangas-Ramírez E, Sarma S S S, Nandini S. Acute and chronic toxicity of ammonium chloride to the cladoceran Daphnia pulex Leydig in relation to algal food density [J]. Bulletin of Environmental Contamination and Toxicology, 2001,67(6): 834-840.
[35]
Mangas-Ramírez E, Sarma S S S, Nandini S. Combined effects of algal (Chlorella vulgaris) density and ammonia concentration on the population dynamics of Ceriodaphnia dubia and Moina macrocopa (Cladocera) [J]. Ecotoxicology and Environmental Safety, 2002,51(3):216-222.
[36]
Ramírez-Pérez T, Sarma S S S, Nandini S. Effects of mercury on the life table demography of the rotifer Brachionus calyciflorus Pallas (Rotifera) [J]. Ecotoxicology, 2004,13(6):535-544.
[37]
Gentile J H, Gentile S M, Hairston Jr N G. The use of life tables for evaluating the chronic toxicity of pollutants to Mysidopsisbahia [J]. Hydrobiologia, 1982,93(1):179-187.
[38]
Rao T R, Sarma S S S. Demographic parameters of Brachionus patulus Muller (Rotifera) exposed to sublethal DDT concentrations at low and high food levels [J]. Hydrobiologia, 1986,139(3):193-200.
[39]
Day K, Kaushik N K. An assessment of the chronic toxicity of the synthetic pyrethriod, fenvalerate, to Daphniagaleata mendoate, using life table [J]. Environmental Pollution, 1987,44(1):13-26.
[40]
Boyum K W, Brooks A S. The effect of selenium in water and food on Daphnia populations [J]. Archives of Environmental Contamination and Toxicology, 1988,17(5):555-560.
[41]
Xi Y L, Hu H Y. Effect of thiophanate-methyl on the reproduction and survival of the refreshwater rotifer Brachionus calyciflorus pallas [J]. Bulletin of Environmental Contamination and Toxicology, 2003,71(4):722-728.
[42]
Ferrando M D, Sancho E, Andreu-Moliner E. Chronic toxicity of fenitrothion to an algae (Nannochloropsis oculata), a rotifer (Brachionus calyciflorus), and the cladoceran (Daphnia magna) [J]. Ecotoxicology and Environmental Safety, 1996,35(2): 112-120.
[43]
Janssen C R, Persoone G, Snell T W. Cyst-based toxicity test Ⅷ. Short-chronic toxicity test with the freshwater rotifer Brachionus calyciflorus [J]. Aquatic Toxicology, 1994,28(3/4):243-258.
Serbus L R, Casper-Lindley, Landmann F. The genetics and cell biology of Wolbachia-host interactions [J]. Annual Review of Genetics, 2008,42(42):683-707.
[48]
Werren J H, Laura B, Clark M E. Wolbachia: master manipulators of invertebrate biology [J]. Nature Reviews Microbiology, 2008,6(10):741-751.
[49]
Hilgenboecker K, Hammerstein P, Schlattmann P, et al. How many species are infected with Wolbachia? -A statistical analysis of current data [J]. Fems Microbiology Letters, 2008,281(2):215-220.