Selenium (Se) leaches into water from agricultural soils and from storage
sites for coal fly ash. Se toxicity causes population and community level
effects in fishes and birds. We used the laboratory aquarium model fish,
Japanese medaka (Oryzias latipes), an asynchronous breeder, to
determine aspects of uptake in adults and resultant developmental toxicity in
their offspring. The superior imaging properties of the model enabled detailed
descriptions of phenotypic alterations not commonly reported in the existing Se
literature. Adult males and females in treatment groups were exposed, separately
and together, to a dry diet spiked with 0, 12.5, 25, or 50 µg/g (dry
weight) seleno-L-methionine (SeMet) for 6 days, and their embryo progeny
collected for 5 days, maintained under controlled conditions and observed daily
for hatchability, mortality and/or developmental toxicity. Sites of alteration
included: craniofacial, pericardium and abdomen (Pc/Ab), notochord, gall
bladder, spleen, blood, and swim bladder. Next, adult tissue Se concentrations
(liver, skeletal muscle, ovary and testis) were determined and compared in
treatment groups of bred and unbred individuals. No significant difference was
found across treatment groups at the various SeMet concentrations; and,
subsequent analysis compared exposed vs. control in each of the treatment groups
at 10 dpf. Increased embryo mortality was observed in all treatment groups,
compared to controls, and embryos had a decreased hatching rate when both
parents were exposed. Exposure resulted in significantly more total altered
phenotypes than controls. When altered phenotypes following exposure of both
parents were higher than maternal only exposure, a male role was suggested. The
comparisons between treatment groups revealed that particular types of
phenotypic change may be driven by the sex of the exposed parent. Additionally,
breeding reduced Se concentrations in some adult tissues, specifically the liver
of exposed females and skeletal muscle of exposed males. Detailed phenotypic
analysis of progeny from SeMet exposed parents should inform investigations of
later life stages in an effort to determine consequences of early life
exposure.