Minerals excreted in feces have the potential to leach or runoff to water-ways, negatively impacting water quality. This study examined the effect of dietary trace mineral levels, and their source, on the leaching potential of minerals from equine feces. Nine horses were used in a replicated 3 × 3 Latin Square, with three dietary treatments provided as pellets: no added trace minerals (CON), added inorganic trace minerals (ING), and added organic trace minerals (ORG). Supplemental trace minerals included Co, Cu, Mn, and Zn. Horses were allowed ad libitum access to forage and fed their treatment pellets for 16 days prior to fecal sample collection. Estimated dietary mineral intake exceeded requirements for supplemented minerals. Regardless of the source, adding dietary trace minerals increased the fecal leaching potential of Cu, Zn, and P (p < 0.05). More Co leached from ORG compared to ING, while Zn leached in greater amounts from ING compared to ORG (p < 0.05). Fecal bacterial Zn content was greater (p < 0.05) for ORG compared to ING. Negative correlations were observed between bacterial mineral content and leaching for several minerals. Supplementing trace minerals in forms that increase microbial incorporation may provide a strategy to control fecal mineral leaching.

Ergot alkaloids, in their active isomeric form, affect animal health and performance, and adsorbents are used to mitigate toxicities by reducing bioavailability. Adsorbents with high specificity (molecularly imprinted polymers: MIP) adsorb ergot alkaloids in vitro, but require evaluation for biological implications. Using ex vivo myography, synthetic polymers were evaluated for effects on the bioactivity of ergotamine tartrate (ETA). Polymers were first evaluated using isotherms. Lateral saphenous veins were collected from 17 steers for four independent studies: dose response of ETA, adsorbent dose response, validation of pre-myograph incubation conditions and MIP/ non-molecularly imprinted polymer (NIP) comparison. Norepinephrine normalized percent contractile response to increasing ETA exhibited a sigmoidal dose response (max: 88.47 and log of the effective molar concentration (EC₅₀) (−log [ETA]) of 6.66 ± 0.17 M). Although sample preparation time affected contractile response (p < 0.001), pre-myograph incubation temperature (39 vs. 21 °C, 1 h) had no effect (p > 0.05). Isothermal adsorption showed a maximum adsorption of 3.27E-008 moles·mg⁻¹ and affinity between 0.51 and 0.57 mg (R²: 0.83–0.92) for both polymers, with no significant difference between polymers (p > 0.05). No significant differences in maximum inhibitory (p = 0.96) and IC₅₀ responses (p = 0.163) between MIP and NIP were noticed. Normalized percent contraction could be predicted from the in vitro adsorption data (R² = 0.87, p < 0.01), for both polymers. These studies indicate that synthetic polymers are potentially effective adsorbents to mitigate ergot toxicity caused by ergot alkaloids, with little evidence of significant differences between MIP and NIP in aqueous media.