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Water chemistry of Blue Lake, Central Otago

Personnel:

  • Sean Barker (geochemist)

  • Jon Kim (water chemist)

  • Russell Frew (isotope chemist)

  • Dave Craw (geologist)

Fig 1

Blue Lake is an abandoned alluvial gold mine located at the town of St. Bathans, in Central Otago. The mine was worked sporadically up to the 1940s, and was then abandoned and subsequently filled with water. The resulting pit lake is now considered a local amenity for swimming and boating, in an area with low population and little human development. 

Fig 2

Locality map of northern Central Otago. Blue Lake lies at the foot of the St Bathans Range, at the old gold-mining town of St Bathans. This is a low-rainfall area with high evaporation.

Blue Lake was excavated at the west-sloping boundary between basement rocks and younger sediments. The basement rocks consist of greywacke and argillite similar to that which occurs throughout Canterbury to the north. These rocks are generally hard and resistant to erosion, although the argillite breaks into small fragments in cliffs. Near the gold-bearing boundary, the basement rocks have been extensively altered by groundwater to form soft clay.

Fig 3

View of Blue Lake, looking north to Mt St Bathans, which is made of greywacke basement. Greywacke and argillite basement rocks, with their clay-rich alteration, form the sluiced slopes in the right distance, sloping down to the left into the lake. The rest of the white exposed material is quartz conglomerate. Gold was mined from the quartz conglomerate near to the boundary with the basement rocks.

 

The greywacke basement rocks are overlain by 10-20 million year old river and lake sediments, including some lignite.  At Blue Lake, these sediments are mainly white conglomerate consisting of quartz pebbles. The quartz conglomerate contains alluvial gold, particularly near the base of the formation where it rests on the altered basement rocks. Hence, gold mining at Blue Lake was focussed on this portion of the formation, and the miners followed the dipping strata downwards to the west, exposing the basement alteration surface in the process. Mining eventually became uneconomic as the gold-bearing stratum was followed downwards, and when it ceased, the mine filled with water to form Blue Lake.
The water in Blue Lake has accumulated since the end of mining (>60 yrs) from surface and ground water in the immediate vicinity of the mine. There is no regular outlet, except during major rain events, so evaporation is the main way that accumulated water is discharged. The water is slightly alkaline at the surface, and the pH rises to near-neutral (pH = 7) near the bottom of the lake. This high pH is caused by input of groundwater that has dissolved calcium carbonate (calcite) from the basement greywacke, and is typical of rivers in the area. Most of the lake is well-oxygenated, but there is a low-oxygen layer at the bottom. The chemical change near the bottom coincides with a distinct temperature change (thermocline) from 14°C near the surface, to 6.5°C at the bottom.

Fig 4

Profiles of pH and dissolved oxygen with depth through Blue Lake water. Water has distinctly different composition near the bottom compared to the surface water.

 

 

The oxygen and hydrogen isotope ratios of water in nearby rivers are typical of precipitation of the area. They lie close to the meteoric (rain) water values for Central Otago and the relatively light values (d18O near -11‰) reflects the rain shadow setting for this precipitation. In contrast, Blue Lake water has distinctly heavier d18O and d2H ratios (near -7‰ and –55‰, respectively). The 5‰ rise in d18O requires at least two-fold evaporative concentration of lake waters. There has also been a 3-5 fold evaporative enrichment of the major cations: Na+, K+, Mg2+, and Ca2+ compared to river waters.
There are large differences in SO42- concentrations between Blue Lake and nearby stream waters. High concentrations of SO42- in the lake waters (c. 24 times the nearby streams) reflect the evaporative concentration of Blue Lake, with additional input from adjacent rocks. Basement argillite contains scattered pyrite (FeS2), and the quartz conglomerate also contains pyrite, especially near to lignite layers. Weathering of all these rocks in this dry climate results in white and yellow surface crusts on outcrops containing sulfate minerals. Rainwater runoff transfers dissolved sulfate to the lake. There is sufficient dissolved bicarbonate in the lake to neutralize any acidic ground water inputs to the lake.

Fig 5

Comparison of common dissolved material in Blue Lake waters and nearby rivers. Bicarbonate and silica are in similar proportions in rivers and Blue Lake. Blue Lake has much higher proportion of sulfate derived from S-bearing minerals in the surrounding rocks

 

Localised acidification in surface and ground waters occurs during oxidation of pyrite. This acidification causes metals to dissolve from the surrounding rocks. Most metals are mobilised by oxidation of pyrite in basement argillite. This results in the lake waters being enriched in dissolved Zn compared to nearby stream waters which are dominated by dissolved Cu. Iron and Zn may be partly removed from solution by adsorption on to settling particulate iron oxyhydroxides, but lake bottom sediments show only minor evidence of such metal enrichment.

Fig 6

Variations in dissolved trace metal concentrations with depth in Blue Lake.  Concentrations are measured in parts per billion (ppb).

 

The major processes affecting the chemical composition of the major ions and trace metals of Blue Lake are summarised in the diagram below.  These are all natural processes, which occur within the lake catchment itself. Evaporative concentration and input of trace metals by surface and ground waters due to geochemical weathering of sulfide minerals are the main processes. In general, metal enrichment in lake waters and bottom sediments will probably continue to occur into the future.  While the observed dissolved trace metal concentrations for Zn and Cu in Blue Lake water (50 and 20 nmol/L, respectively) are near the threshold for incipient toxicity of aqueous ecosystems, level of dissolved Ni (44 nmol/L) is significantly lower and is not a potential issue. The bioavailability of the dissolved Zn, Ni and Cu in Blue Lake is at present unknown. 

Fig 7

Variations in dissolved trace metal concentrations with depth in Blue Lake.  Concentrations are measured in parts per billion (ppb).

 

 

Further information:

  • Blue Lake and how the gold got there

  • Barker, S L L, Kim, J P, Craw, D, Frew, R D & Hunter, K A. 2004. Processes affecting the chemical composition of Blue Lake, an alluvial gold-mine pit lake in New Zealand. Marine and Freshwater Research 55: 201-211.

 

 

 

 

 

 

 

Environmental Science photo

 
Environmental Science photo
 
Environmental Science photo

 

 
University of Otago Environmental Science