Intersex (testicular oocytes) in smallmouth bass from the Potomac River and selected nearby drainages.

Intersex, or the presence of characteristics of both sexes, in fishes that are normally gonochoristic has been used as an indicator of exposure to estrogenic compounds. In 2003, during health assessments conducted in response to kills and a high prevalence of skin lesions observed in smallmouth bass Micropterus dolomieu in the South Branch of the Potomac River, the presence of immature oocytes within testes was noted. To evaluate this condition, a severity index (0-4) was developed based on the distribution of oocytes within the testes. Using gonad samples collected from 2003 to 2005, the number of histologic sections needed to accurately detect the condition in mature smallmouth bass was statistically evaluated. The reliability of detection depended on the severity index and the number of sections examined. Examining five transverse sections taken along the length of the gonad resulted in a greater than 90% probability of detecting testicular oocytes when the severity index exceeded 0.5. Using the severity index we compared smallmouth bass collected at selected sites within the South Branch during three seasons in 2004. Seasonal differences in severity and prevalence were observed. The highest prevalence and severity were consistently noted during the prespawn-spawning season, when compared with the postspawn season. In 2005, smallmouth bass were collected at selected out-of-basin sites in West Virginia where fish kills and external skin lesions have not been reported, as well as at sites in the Shenandoah River, Virginia (part of the Potomac drainage), where kills and lesions occurred in 2004-2005. The prevalence of testicular oocytes is discussed in terms of human population and agricultural intensity.

[1]  Mary Formanowicz,et al.  United States Census 1900 , 1907 .

[2]  Y. Okada A Further Note on Testis-Ova in the Teleost, Oryzias latipes , 1964 .

[3]  S. Hamaguchi,et al.  Evidence for the sexual bipotentiality of spermatogonia in the fish, Oryzias latipes. , 1988, The Journal of experimental zoology.

[4]  J. Sumpter,et al.  Estrogenic Effects of Effluents from Sewage Treatment Works , 1994 .

[5]  T. C. Daniel,et al.  Runoff of estrogen hormone 17β-estradiol from poultry litter applied to pasture , 1997 .

[6]  John P. Sumpter,et al.  Widespread Sexual Disruption in Wild Fish , 1998 .

[7]  Edwin J. Routledge,et al.  Identification of Estrogenic Chemicals in STW Effluent. 1. Chemical Fractionation and in Vitro Biological Screening , 1998 .

[8]  J. Sumpter,et al.  Demasculinisation of sexually mature male common carp, Cyprinus carpio, exposed to 4-tert-pentylphenol during spermatogenesis , 1998 .

[9]  C. Metcalfe,et al.  Factors affecting the development of testis‐ova in medaka, Oryzias latipes, exposed to octylphenol , 1999 .

[10]  D. Tillitt,et al.  Biomonitoring of Environmental Status and Trends (BEST) Program: Field Procedures for Assessing the Exposure of Fish to Environmental Contaminants , 1999 .

[11]  A. Scott,et al.  Survey of estrogenic activity in United Kingdom estuarine and coastal waters and its effects on gonadal development of the flounder Platichthys flesus , 1999 .

[12]  J. Nagler,et al.  Induction of gonadal intersex in genotypic male rainbow trout (Oncorhynchus mykiss) embryos following immersion in estradiol‐17ß , 2000, Molecular reproduction and development.

[13]  K. Schramm,et al.  Endocrine disruption by hexachlorobenzene in Crucian carp (Carassius auratus gibelio). , 2000, Bulletin of environmental contamination and toxicology.

[14]  A. Kortenkamp,et al.  Prediction and assessment of the effects of mixtures of four xenoestrogens. , 2000, Environmental health perspectives.

[15]  S. Teh,et al.  Determining the sensitive developmental stages of intersex induction in medaka (Oryzias latipes) exposed to 17 beta-estradiol or testosterone. , 2000, Marine environmental research.

[16]  Y. Oshima,et al.  Effect of bisphenol a on the early life stage in Japanese medaka (Oryzias latipes) , 2000 .

[17]  C. Metcalfe,et al.  Gonadal development and endocrine responses in Japanese medaka (Oryzias latipes) exposed to o,p′‐DDT in water or through maternal transfer , 2000 .

[18]  T. Iguchi,et al.  Elevated serum vitellogenin levels and gonadal abnormalities in wild male flounder (Pleuronectes yokohamae) from Tokyo Bay, Japan. , 2000, Marine environmental research.

[19]  J. Harshbarger,et al.  Intersexes in Mississippi River shovelnose sturgeon sampled below Saint Louis, Missouri, USA. , 2000, Marine environmental research.

[20]  L. Viganò,et al.  First observation of intersex cyprinids in the Po River (Italy). , 2001, The Science of the total environment.

[21]  J. Sumpter,et al.  A histological description of intersexuality in the roach , 2001 .

[22]  J. Sumpter,et al.  Sexual disruption in a second species of wild cyprinid fish (the gudgeon, Gobio gobio) in United Kingdom Freshwaters , 2001, Environmental toxicology and chemistry.

[23]  Masanori Seki,et al.  Effect of ethinylestradiol on the reproduction and induction of vitellogenin and testis‐ova in medaka (Oryzias latipes) , 2002, Environmental toxicology and chemistry.

[24]  J. Sumpter,et al.  Wild Intersex Roach (Rutilus rutilus) Have Reduced Fertility1 , 2002, Biology of reproduction.

[25]  A. Kortenkamp,et al.  Combining xenoestrogens at levels below individual no-observed-effect concentrations dramatically enhances steroid hormone action. , 2002, Environmental health perspectives.

[26]  I. Kang,et al.  Effect of 17β-estradiol on the reproduction of Japanese medaka (Oryzias latipes) , 2002 .

[27]  M. I C H A E,et al.  Pharmaceuticals, Hormones, and Other Organic Wastewater Contaminants in U.S. Streams, 1999-2000: A National Reconnaissance , 2002 .

[28]  J. Gercken,et al.  Intersex in feral marine and freshwater fish from northeastern Germany. , 2002, Marine environmental research.

[29]  J. Sumpter,et al.  Altered Sexual Maturation and Gamete Production in Wild Roach (Rutilus rutilus) Living in Rivers That Receive Treated Sewage Effluents1 , 2002, Biology of reproduction.

[30]  E. Michael Thurman,et al.  Response to Comment on “Pharmaceuticals, Hormones, and Other Organic Wastewater Contaminants in U.S. Streams, 1999−2000: A National Reconnaissance” , 2002 .

[31]  J. Zelikoff,et al.  Biochemical and toxicopathic biomarkers assessed in smallmouth bass recovered from a polychlorinated biphenyl-contaminated river , 2003, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.

[32]  D. Kime,et al.  Evidence of a high percentage of intersex in the Mediterranean swordfish (Xiphias gladius L.). , 2003, Marine pollution bulletin.

[33]  C. Metcalfe,et al.  Effects of the isoflavones genistein and equol on the gonadal development of Japanese medaka Oryzias latipes. , 2003, Environmental health perspectives.

[34]  J. Sumpter,et al.  Stress status of gudgeon (Gobio gobio) from rivers in Switzerland with and without input of sewage treatment plant effluent. , 2003, Environmental toxicology and chemistry.

[35]  Ann C Wilkie,et al.  Manure-borne estrogens as potential environmental contaminants: a review. , 2003, Environmental science & technology.

[36]  K. Bateman,et al.  A ranking system for the evaluation of intersex condition in european flounder (Platichthys flesus) , 2004, Environmental toxicology and chemistry.

[37]  D. Marcogliese,et al.  Consequences of xenoestrogen exposure on male reproductive function in spottail shiners (Notropis hudsonius). , 2004, Toxicological sciences : an official journal of the Society of Toxicology.

[38]  T. J. Leiker,et al.  A holistic passive integrative sampling approach for assessing the presence and potential impacts of waterborne environmental contaminants. , 2004, Chemosphere.

[39]  Ana M Soto,et al.  Endocrine-disrupting effects of cattle feedlot effluent on an aquatic sentinel species, the fathead minnow. , 2003, Environmental health perspectives.

[40]  C. Tyler,et al.  Impacts of 17β-estradiol, including environmentally relevant concentrations, on reproduction after exposure during embryo-larval-, juvenile- and adult-life stages in zebrafish (Danio rerio) , 2004 .

[41]  Eiji Katsura,et al.  Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells. , 2004, Environmental health perspectives.

[42]  C. Metcalfe,et al.  Endocrine disruption and altered gonadal development in white perch (Morone americana) from the lower Great Lakes region. , 2004, Environmental health perspectives.

[43]  Andreas Kortenkamp,et al.  Sediments are major sinks of steroidal estrogens in two United Kingdom rivers , 2004, Environmental toxicology and chemistry.

[44]  J. van Vuren,et al.  Histological evidence of intersex in feral sharptooth catfish (Clarias gariepinus) from an estrogen‐polluted water source in Gauteng, South Africa , 2004, Environmental toxicology.

[45]  C. Tyler,et al.  Assessing the Sensitivity of Different Life Stages for Sexual Disruption in Roach (Rutilus rutilus) Exposed to Effluents from Wastewater Treatment Works , 2005, Environmental health perspectives.

[46]  Shoko Imai,et al.  Effects of 17beta-estradiol on the reproduction of Java-medaka (Oryzias javanicus), a new test fish species. , 2005, Marine pollution bulletin.

[47]  M. Morita,et al.  Feminization of Japanese medaka (Oryzias latipes) exposed to 17beta-estradiol: formation of testis-ova and sex-transformation during early-ontogeny. , 2006, Aquatic toxicology.

[48]  D. O. Norris,et al.  Intersex and other reproductive disruption of fish in wastewater effluent dominated Colorado streams. , 2006, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.

[49]  P. Bjerregaard,et al.  Intersex in wild roach (Rutilus rutilus) from Danish sewage effluent-receiving streams. , 2006, Ecotoxicology and environmental safety.

[50]  C. Metcalfe,et al.  Developmental effects in Japanese medaka (Oryzias latipes) exposed to nonylphenol ethoxylates and their degradation products. , 2006, Chemosphere.

[51]  Paul D. Jones,et al.  Terminology of gonadal anomalies in fish and amphibians resulting from chemical exposures. , 2006, Reviews of environmental contamination and toxicology.

[52]  V. Blazer,et al.  Polychlorinated biphenyls, mercury, and potential endocrine disruption in fish from the Hudson River, New York, USA , 2006, Aquatic Sciences.

[53]  C. Porte,et al.  Evidence of endocrine alteration in the red mullet, Mullus barbatus from the NW Mediterranean. , 2006, Environmental pollution.

[54]  Y. Takeuchi,et al.  Testicular germ cells can colonize sexually undifferentiated embryonic gonad and produce functional eggs in fish. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[55]  T. J. Leiker,et al.  A Reconnaissance for Emerging Contaminants in the South Branch Potomac River, Cacapon River, and Williams River Basins, West Virginia, April-October 2004 , 2006 .

[56]  Richard J. Williams,et al.  Predicted Exposures to Steroid Estrogens in U.K. Rivers Correlate with Widespread Sexual Disruption in Wild Fish Populations , 2005, Environmental health perspectives.

[57]  C. A. Harris,et al.  Evidence of estrogenic mixture effects on the reproductive performance of fish. , 2007, Environmental science & technology.

[58]  P. Bjerregaard,et al.  Effects of the fungicide prochloraz on the sexual development of zebrafish (Danio rerio). , 2007, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.