Lake Victoria during its geological history, went through changes
ranging from its present shallow depression, through to what may have been a series
of much smaller lakes. Geological cores taken from its bottom show Lake
Victoria has dried up completely at least three times since it formed. These
drying cycles are probably related to past ice ages, which were times when precipitation
declined globally. Lake Victoria last dried out 17,300 years ago, and it
refilled beginning about 14,700 years ago. Geologically, Lake Victoria is
relatively young – about 400,000 years old – and it formed when
westward-flowing rivers were dammed by an upthrown crustal block.
This geological history probably contributed to the dramatic
cichlid speciation that characterises its ecology, as well as that of other
African Great Lakes, although some researchers dispute this, arguing while Lake
Victoria was at its lowest between 18,000 and 14,000 years ago, and it dried
out at least once during that time, there is no evidence of remnant ponds or
marshes persisting within the desiccated basin. If such features existed, then
they would have been small, shallow, turbid, and/or saline, and therefore
markedly different from the lake to which today's species are adapted.
The shallowness of Lake Victoria, its limited river inflow,
and its large surface area compared to its volume make it vulnerable to the
effects of climate changes.
Hydrology and limnology
Lake Victoria receives 80% of its water from direct
precipitation. Average evaporation on the lake is between 2.0 and 2.2 metres 6.6
and 7.2 ft per year, almost double the precipitation of riparian areas. In the
Kenya Sector, the main influent rivers are the Sio, Nzoia, Yala, Nyando, Sondu
Miriu, Mogusi and the Migori. Combined, these rivers contribute far more water to
the lake than does the largest single inflowing river, the Kagera River, which
enters the lake from the west.
Lake Victoria and the Great Rift Valley
The only outflow from Lake Victoria is the Nile River which
exits the lake near Jinja, Uganda. In terms of contributed water, this makes
Lake Victoria the principal source of the longest branch of the Nile, however,
the most distal source of the Nile Basin, and therefore the ultimate source of
the Nile, is more often considered to be one of the tributary rivers of the
Kagera River the exact tributary remains undetermined, and which originates in
either Rwanda or Burundi. The uppermost section of the Nile is generally known
as the Victoria Nile until it reaches Lake Albert. Although it is a part of the
same river system known as the White Nile and is occasionally referred to as
such, strictly speaking this name does not apply until after the river crosses
the Uganda border into South Sudan to the north.
The lake exhibits eutrophic conditions. In 1990–1991, oxygen
concentrations in the mixed layer were higher than in 1960–1961, with nearly
continuous oxygen supersaturation in surface waters. Oxygen concentrations in
hypolimnetic waters i.e. the layer of water that lies below the thermocline, is
noncirculating, and remains perpetually cold were lower in 1990–1991 for a
longer period than in 1960–1961, with values of less than 1 mg per litre <
0.4 gr/cu ft occurring in water as shallow as 40 metres compared with a
shallowest occurrence of greater than 50 metres in 1961. The changes in
oxygenation are considered consistent with measurements of higher algal biomass
and productivity. These changes have arisen for multiple reasons: successive
burning within its basin, soot and ash from which has been deposited over the
lake's wide area; from increased nutrient inflows via rivers, and from
increased pollution associated with settlement along its shores.
The extinction of cichlids in the genus Haplochromis has
also been blamed on the lake's eutrophication. The fertility of tropical waters
depends on the rate at which nutrients can be brought into solution. The
influent rivers of Lake Victoria provide few nutrients to the lake in relation
to its size. Because of this, most of Lake Victoria's nutrients are thought to
be locked up in lake-bottom deposits. By itself, this vegetative matter decays
slowly. Animal flesh decays considerably faster, however, so the fertility of
the lake is dependent on the rate at which these nutrients can be taken up by
fish and other organisms. There is little doubt that Haplochromis played an
important role in returning detritus and plankton back into solution. With some
80% of Haplochromis species feeding off detritus, and equally capable of
feeding off one another, they represented a tight, internal recycling system,
moving nutrients and biomass both vertically and horizontally through the water
column, and even out of the lake via predation by humans and terrestrial
animals. The removal of Haplochromis, however, may have contributed to the
increasing frequency of algal blooms, which may in turn be responsible for mass
fish kills.
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