posted on 2016-02-09, 17:14authored byPatrick M. Donovan, Joel D. Blum, Michael
Bliss Singer, Mark Marvin-DiPasquale, Martin T. K. Tsui
We measured total mercury (THg) and monomethyl mercury (MMHg) concentrations
and mercury (Hg) isotopic compositions in sediment and aquatic organisms
from the Yuba River (California, USA) to identify Hg sources and biogeochemical
transformations downstream of a historical gold mining region. Sediment
THg concentrations and δ202Hg decreased from the
upper Yuba Fan to the lower Yuba Fan and the Feather River. These
results are consistent with the release of Hg during gold mining followed
by downstream mixing and dilution. The Hg isotopic composition of
Yuba Fan sediment (δ202Hg = −0.38 ± 0.17‰
and Δ199Hg = 0.04 ± 0.03‰; mean ±
1 SD, n = 7) provides a fingerprint of inorganic
Hg (IHg) that could be methylated locally or after transport downstream.
The isotopic composition of MMHg in the Yuba River food web was estimated
using biota with a range of %MMHg (the percent of THg present as MMHg)
and compared to IHg in sediment, algae, and the food web. The estimated
δ202Hg of MMHg prior to photodegradation (−1.29
to −1.07‰) was lower than that of IHg and we suggest
this is due to mass-dependent fractionation (MDF) of up to −0.9‰
between IHg and MMHg. This result is in contrast to net positive MDF
(+0.4 to +0.8‰) previously observed in lakes, estuaries, coastal
oceans, and forests. We hypothesize that this unique relationship
could be due to differences in the extent or pathway of biotic MMHg
degradation in stream environments.