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Effects of pharmaceuticals on Daphnia survival, growth, and reproduction [An article from: Chemosphere]

Author C.M. Flaherty, S.I. Dodson
Publisher Elsevier
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Book Details
PublisherElsevier
ISBN / ASINB000RR5HJU
ISBN-13978B000RR5HJ7
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States 🇺🇸

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This digital document is a journal article from Chemosphere, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Pharmaceuticals have been globally detected in surface waters, and the ecological impacts of these biologically-active, ubiquitous chemicals are largely unknown. To evaluate the aquatic toxicity of individual pharmaceuticals and mixtures, we performed single species laboratory toxicity tests with Daphnia magna, a common freshwater zooplankton. We conducted acute (6-day) and chronic (30-day) exposure pharmaceutical bioassays and evaluated survivorship and morphology of adults and neonates, adult length, resting egg production, brood size (fecundity), and the proportion of male broods produced (sex ratio). In general, exposure to a single pharmaceutical in the 1-100@mg/l range yielded no apparent effects on the normal life processes of Daphnia. However, chronic fluoxetine exposure (36@mg/l) significantly increased Daphnia fecundity, and acute clofibric acid exposure (10@mg/l) significantly increased sex ratio. A mixture of fluoxetine (36@mg/l) and clofibric acid (100@mg/l) caused significant mortality; the same fluoxetine concentration mixed with 10@mg/l clofibric acid resulted in significant deformities, including malformed carapaces and swimming setae. Mixtures of three to five antibiotics (total antibiotic concentration 30-500@mg/l) elicited changes in Daphnia sex ratio. We conclude: (1) individual and mixtures of pharmaceuticals affect normal development and reproduction of Daphnia magna, (2) aquatic toxicity of pharmaceutical mixtures can be unpredictable and complex compared to individual pharmaceutical effects, and (3) timing and duration of pharmaceutical exposure influence aquatic toxicity.