Description and potential sources of a shell deformity in North American freshwater mussels (Unionoida).

Objective: Freshwater mussels of the order Unionoida are among the most imperiled taxa in North America, and many species are undergoing enigmatic decline without fully understood causation. Disease pathology and parasitology have been identified as areas with significant knowledge gaps in relation to these declines. We investigated a shell deformity of unknown cause that is widespread in northeastern North America by adding to the clinical description from a mussel assemblage in Massachusetts with a deformity prevalence exceeding 50%.

Chronic fluoxetine exposure alters movement and burrowing in adult freshwater mussels.

The antidepressant fluoxetine is commonly found in aquatic fauna living near or downstream from point-sources of municipal waste effluent. Continuous release of fluoxetine results in increased effective exposure duration in surface waters, resulting in a chronic exposure for animals downstream, particularly in effluent dominated ecosystems. Fluoxetine is known to cause disruptions in reproductive behavior of freshwater mussels (order Unionoida), including stimulating release of gametes, parturition of glochidia (larvae), and changes in lure display and foot protrusion.

Fluoxetine alters adult freshwater mussel behavior and larval metamorphosis.

We used acute and partial-lifecycle tests to examine the effects of the pharmaceutical fluoxetine on freshwater mussels (Unionida). In acute tests lasting 24-48 h, we determined median effective concentrations (EC50s) for fluoxetine with larval (glochidia viability) and juvenile (survival) life-stages of fatmucket (Lampsilis siliquoidea) and black sandshell (Ligumia recta). In a 28-d behavioral test we exposed brooding adult female wavy-rayed lampmussels (Lampsilis fasciola) to 0.

Partial life-cycle and acute toxicity of perfluoroalkyl acids to freshwater mussels.

Freshwater mussels are among the most sensitive aquatic organisms to many contaminants and have complex life-cycles that include several distinct life stages with unique contaminant exposure pathways. Standard acute (24-96 h) and chronic (28 d) toxicity tests with free larva (glochidia) and juvenile mussels are effective at generating data on contaminant effects at two discrete life stages but do not incorporate effects on brooded glochidia. We developed a novel partial life-cycle assay that incorporates exposures to brooding adult female mussels and used this method in combination with acute toxicity tests to assess adverse effects of perfluoroctanesulfonic acid (PFOS) and perfluoroctanoic acid (PFOA) on freshwater mussels.