Small- and medium-scale mining operations in Guyana have increased significantly since the late 1980s. The majority of these gold mining operations utilize mercury (Hg) amalgamation methods in the recovery process, raising the question as to the significance of Hg inputs to the environment from mining activities. In March and April, 2001, 168 samples were collected from floodplain, sand bar, and channel bed deposits along a 350 km reach of the Mazaruni River and a 160 km reach of the Essequibo River. Distinct trends in the geochemical data suggest that much of the Hg found in the alluvial deposits is related to anthropogenic sources, including (1) Hg concentrations in floodplain, channel bed and sand bar deposits locally exceed background values defined by ferralitic soils; (2) core data reveal that Hg concentrations within floodplain deposits have increased in recent years; and (3) high Hg concentrations along the channels can be attributed to the influx of material from tributaries affected by mining operations, or to mining activities along the rivers. Recent investigations in Amazonia have argued that Hg from amalgamation mining represents a small portion of the total Hg load to riverine systems, the majority coming from the erosion of Hg enriched upland soils within deforested terrain. Geochemical data from the Essequibo and Mazaruni Rivers suggest that Hg from mining may be a more significant source in Guyana where large-scale deforestation is limited. However, it is unclear whether the increased Hg represents the direct input associated with the amalgamation process, or Hg associated with the erosion of soils and sediments that results from activities that accompany mining.

Assessing metal contamination of sediments requires knowledge of the geochemical partitioning of trace metals at the sediment-water interface. Under controlled laboratory conditions, sequential extraction was conducted to determine the associations of metals (Cd, Cr, and Zn) and radiotracers (¹⁰⁹Cd,⁵¹Cr, and⁶⁵Zn) with various geochemical phases and the different partitioning and mobility of metals for two types of surface sediments collected from the Huanghe and Changjiang Rivers in Eastern China. The residual phase was the major phase for stable metal binding, indicating that these sediments had little subjection to recent anthropogenic influences. Fe–Mn oxides were the next important binding phases for metals. The partitioning of metals in various geochemical phases as a function of the duration of the radiolabeling was also examined. Trace metals transferred among the different geochemical phases over the 30 days radiolabeling period, particularly between the carbonate and Fe–Mn oxides phases. The freshwater-sediment distribution coefficients (Kd) of three metals were investigated in batch experiments using the radiotracer technique. The decreasing Kdwith increasing metal concentration(from 0.5 to 200 μg L⁻¹) may be explained by competitive adsorption. The metal Kdin sediments from the Changjiang River was greater than those from the Huanghe River, presumably because of the higher Fe/Mn and organic carbon contents in Changjiang River sediment. The Kddecreased with increasing total suspended solid load from 3 to 500 mg L⁻¹, and was Cr > Zn > Cd. For Cd and Zn, increasing the pH from 5 to 8 resulted in an increase in Kddue to the reduced H⁺competition and increasing sorptionpotential. However, the Kdfor Cr in the sediments from both rivers showed no relationship with pH, presumably becauseof the complexity of the Cr species and environmental behavior.