Zinc speciation in Lakes Manapouri and Hayes, New Zealand

2001 ◽  
Vol 52 (2) ◽  
pp. 217 ◽  
Author(s):  
Michael J. Ellwood ◽  
Michael J. Ellwood ◽  
Keith A. Hunter ◽  
Keith A. Hunter ◽  
Jonathan P. Kim ◽  
...  

A study of zinc complexation in Lakes Manapouri and Hayes revealed that zinc speciation in both lakes is dominated by its complexation to natural organic ligands. In Lake Manapouri, dissolved zinc concentrations increased from 0.9 nM in surface waters to ~1.4 nM at depth. Ligand concentrations for this lake were relatively uniform with depth, with values ranging between 2.9 and 4.2 nM. A similar ligand concentration was measured for Lake Hayes, which had a surface zinc concentration of 0.46 nM. Conditional stability constants (log K) for the complexation of zinc to these ligands were high,with values ranging between 10.0 and 11.1. Calculated free Zn 2+ concentrations for both lakes were in the low picomolar range (5—48 pM). Such low free Zn 2+ levels may limit the growth of some phytoplankton in both lakes.

2005 ◽  
Vol 2 (1) ◽  
pp. 56 ◽  
Author(s):  
Sylvia Sander ◽  
Jonathan P. Kim ◽  
Barry Anderson ◽  
Keith A. Hunter

Environmental Context. The bioavailability of dissolved metals in natural waters is directly affected by metal-sequestering agents. These agents include soil-derived matter and compounds released by microorganisms, since copper can support or inhibit aquatic microorganisms depending on concentration. During summer the levels of copper increase in surface waters, an effect intuitively attributable to increased ultraviolet light degrading the sequestering agents more effectively, leading to a concurrent release of the metal. This paper shows that the amount of degradation attributable to light is too low to explain the metal release and that a biological influence may instead be responsible. Abstract. The influence of UVB irradiation on the Cu2+ binding by natural organic ligands in six alpine lakes on the South Island, New Zealand, has been investigated using competitive ligand equilibration with salicylaldoxime and detection by cathodic stripping voltammetry (CLE-CSV). During austral summer 2002–2003 the total dissolved Cu ([Cu]T), the concentration of strong Cu2+-binding ligands ([L]T), and their conditional stability constant K´´ were determined in surface samples of all six lakes. All lakes exhibited appreciable concentrations of a strong Cu2+ binding ligand with similar K´´ values and concentrations always exceeding [CuT], thus dominating Cu2+ speciation. Four lakes (Hayes, Manapouri, Wanaka, Te Anau) showed no appreciable trend in [LT] throughout the summer, whereas in Lakes Wakatipu and Hawea [LT] increased steadily throughout this period. Laboratory UVB irradiation of lake water samples using a 400 W mercury lamp with a Pyrex glass filter (λ > 280 nm) showed that Cu2+-binding ligands are destroyed by UVB radiation, causing [L]T to decrease with a rate of –0.588 nmol L–1 h–1 (r2 0.88). From this we calculate that the in situ ligand destruction rate by UVB in summer for surface waters of these lakes is too small to significantly affect [LT], and conclude that variations in ligand concentrations must result from seasonally variable biological factors.


2007 ◽  
Vol 4 (6) ◽  
pp. 410 ◽  
Author(s):  
Sylvia Sander ◽  
Léticia Ginon ◽  
Barry Anderson ◽  
Keith A. Hunter

Environmental context. The bioavailability of trace metals such as zinc and cadmium strongly depends on what chemical form they are in, and not simply on the total metal concentration. Zinc is an essential micronutrient, whereas cadmium is extremely toxic, but when they occur in the same environment there is potential for the two metals to compete for the same biological binding sites. In this study we have studied the trends in Cd and Zn complexation in three alpine lakes in New Zealand. We conclude that, although the total concentration of cadmium is much lower than that of zinc and copper, it bares the highest risk of toxicity for organisms. Abstract. The variation with depth, pH dependence, seasonal variability and selectivity of strong, natural organic cadmium and zinc-binding ligands from three New Zealand alpine lakes (Hayes, Manapouri and Hauroko) have been investigated. Competitive ligand equilibration–cathodic stripping voltammetry (CLE-CSV) with APDC (ammonium pyrrolidine dithiocarbamate) was used to measure the ligand complexation by Zn2+ and anodic stripping voltammetry (ASV) for complexation of Cd2+. In all lakes, the total dissolved cadmium concentration [CdT] averaged 0.040 nM (standard deviation σ = 0.114), while the average concentration of Cd-binding ligands [LCd] was 5.17 ± 1.79 nM (1σ), with conditional stability constants relative to free Cd2+, log K′Cd2+L′, that ranged from 7.92 at depth to 10.58 at the surface. Calculated concentrations of the free aquo ion [Cd2+] averaged 0.0147 ± 0.0616 nM (1σ), and showed a higher percentage of Cd complexed by strong ligands in the summer and in surface waters. The selectivity of cadmium-binding organic ligands was low, and ligand-bound Cd2+ was easily displaced by Zn2+ and Cu2+. Total dissolved zinc concentrations [ZnT] were highly variable, and ranged from 1.04 to 10.94 nM. The corresponding ligand concentrations of strong zinc-binding ligands [LZn] were between 2.14 and 15.52 nM, with conditional stability constants log K′Zn2+L′ as low as 8.78 in deep water collected in summer from Lake Hauroko, up to a maximum of 12.41 at a depth of 5 m in Lake Hayes. The calculated concentrations of the free aquo complex [Zn2+] ranged widely between 0.001 and 1.620 nM.


1988 ◽  
Vol 22 (11) ◽  
pp. 1381-1388 ◽  
Author(s):  
Jan John ◽  
Brit Salbu ◽  
Egil T. Gjessing ◽  
Helge E. Bjørnstad

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