Microcosm evaluation of the effects of an eight pharmaceutical mixture to the aquatic macrophytes Lemna gibba and Myriophyllum sibiricum

被引:121
作者
Brain, RA
Johnson, DJ
Richards, SM
Hanson, ML
Sanderson, H
Lam, MW
Young, C
Mabury, SA
Sibley, PK
Solomon, KR [1 ]
机构
[1] Univ Guelph, Dept Environm Biol, Ctr Toxicol, Guelph, ON N1G 2W1, Canada
[2] Univ Tennessee, Dept Environm Sci, Chattanooga, TN 37403 USA
[3] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
关键词
pharmaceutical mixture; Myriophyllum sibiricum; Lemna gibba; toxicity; endpoint sensitivity;
D O I
10.1016/j.aquatox.2004.06.011
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Pharmaceuticals have been detected in surface waters of the US and Europe, originating largely from two sources, sewage effluent and agricultural runoff. These compounds often occur as mixtures leading to potential combined effects. In order to investigate the effects of a realistic pharmaceutical mixture on an ecosystem, a study utilizing 15 of 12,000 L aquatic microcosms treated with eight common pharmaceuticals (atorvastatin, acetaminophen, caffeine, sulfamethoxazole, carbamazepine, levofloxacin, sertraline, and trimethoprim) at total (summed) molar concentrations of 0, 0.044, 0.608, 2.664, and 24.538 mumol/L (n = 3) was conducted. Phytotoxicity was assessed on a variety of somatic and pigment endpoints in rooted (Myriophyllum sibiricum) and floating (Lemna gibba) macrophytes over a 35-day period. EC10, EC25 and EC50 values were calculated for each endpoint exhibiting a concentration-dependent response. Generally, M. sibiricum and L. gibba displayed similar sensitivity to the pharmaceutical mixture, with phytotoxic injury evident in both species, which was concentration dependent. Through single compound 7-day daily static renewal toxicity tests with L. gibba, the sulfonamide antibiotic sulfamethoxazole, the fluoroquinolone antibiotic levofloxacin and the blood lipid regulator atorvastatin were found to be the only compounds to elicit phytotoxic effects in the concentration range utilized (0-1000 mug/L). Atorvastatin concentration was highly correlated to decreased pigment content in L. gibba, likely inhibiting the known target enzyme HMGR, the rate-limiting enzyme in isoprenoid biosynthesis. Hazard quotients were calculated for both microcosm and laboratory studies; the highest HQ values were 0.235 (L. gibba) and 0.051 (L. gibba), which are below the threshold value of I for chronic risks. The microcosm data suggest that at an ecological effect size of >20%, biologically significant risks are low for L. gibba and M. sibiricum exposed to similar mixtures of pharmaceutical compounds. For M. sibiricum and L. gibba, respective minimum differences of 5 and 1%, were detectable, however, these effect sizes are not considered ecologically significant. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 40
页数:18
相关论文
共 54 条
[1]  
*ASTM, 1999, 191397 ASTM E, P1434
[2]  
*ASTM, 1998, ANN BOOK ASTM STAND, P784
[3]  
BACH TJ, 1982, BIOCH METABOLISM PLA, P515
[4]   Effects of 25 pharmaceutical compounds to Lemna gibba using a seven-day static-renewal test [J].
Brain, RA ;
Johnson, DJ ;
Richards, SM ;
Sanderson, H ;
Sibley, PK ;
Solomon, KR .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2004, 23 (02) :371-382
[5]   Aquatic ecotoxicology of fluoxetine [J].
Brooks, BW ;
Foran, CM ;
Richards, SM ;
Weston, J ;
Turner, PK ;
Stanley, JK ;
Solomon, KR ;
Slattery, M ;
La Point, TW .
TOXICOLOGY LETTERS, 2003, 142 (03) :169-183
[6]  
CASSEE FR, 1996, TOXICOLOGY CHEM MIXT, V1, P303
[7]  
CHRISTMAN EW, 1994, AQUATIC MESOCOSM STU
[8]   A COMPARISON OF THE EFFECT OF TRICLOPYR TRIETHYLAMINE SALT ON 2 SPECIES OF DUCKWEED (LEMNA) EXAMINED FOR A 7-DAY AND 14-DAY TEST PERIOD [J].
COWGILL, UM ;
MILAZZO, DP ;
LANDENBERGER, BD .
WATER RESEARCH, 1989, 23 (05) :617-623
[9]  
CUPPEN JCM, 1996, ECOTOX ENVIRON SAFE, V38, P25
[10]   Impact of the fungicide carbendazim in freshwater microcosms. I. Water quality, breakdown of particulate organic matter and responses of macroinvertebrates [J].
Cuppen, JGM ;
Van den Brink, PJ ;
Camps, E ;
Uil, KF ;
Brock, TCM .
AQUATIC TOXICOLOGY, 2000, 48 (2-3) :233-250