
Environmental Encyclopedia 3
Heavy metals and heavy metal poisoning
emissions of selected heavy metals/metalloids such as sele-
nium, mercury, arsenic, and antimony. They can be trans-
ported as gases or adsorbed on particles. Other metals such
as cadmium, lead, and zinc are transported atmospherically
only as particles. In either state heavy metals may travel long
distances before being deposited on land or water.
The heavy metal contamination of soils is a far more
serious problem than either air or
water pollution
because
heavy metals are usually tightly bound by the organic compo-
nents in the surface layers of the soil and may, depending
on conditions, persist for centuries or millennia. Conse-
quently, the soil is an important geochemical sink which
accumulates heavy metals rapidly and usually depletes them
very slowly by
leaching
into
groundwater
aquifers or bi-
oaccumulating into plants. However, heavy metals can also
be very rapidly translocated through the environment by
erosion of the soil particles to which they are adsorbed or
bound and redeposited elsewhere on the land or washed into
rivers, lakes or oceans to the
sediment
.
The cycling, bioavailability, toxicity, transport, and
fate of heavy metals are markedly influenced by their phys-
ico-chemical forms in water, sediments, and soils. Whenever
a heavy metal containing
ion
or compound is introduced
into an aquatic environment, it is subjected to a wide variety
of physical, chemical, and biological processes. These in-
clude: hydrolysis, chelation, complexation, redox, biomethy-
lation, precipitation and
adsorption
reactions. Often heavy
metals experience a change in the chemical form or specia-
tion as a result of these processes and so their distribution,
bioavailability, and other interactions in the environment
are also affected.
The interactions of heavy metals in aquatic systems
are complicated because of the possible changes due to many
dissolved and
particulate
components and non-equilibrium
conditions. For example, the speciation of heavy metals is
controlled not only by their chemical properties but also by
environmental variables such as: 1)
pH
; 2) redox potential;
3)
dissolved oxygen
; 4) ionic strength; 5) temperature; 6)
salinity
; 7) alkalinity; 8) hardness; 9) concentration and
nature
of inorganic ligands such as carbonate, bicarbonate,
sulfate, sulfides, chlorides; 10) concentration and nature of
dissolved organic chelating agents such as organic acids,
humic materials,
peptides
, and polyamino-carboxylates; 11)
the concentration and nature of particulate matter with sur-
face sites available for heavy metal binding; and 12) biological
activity.
In addition, various
species
of bacteria can oxidize
arsenate or reduce arsenate to arsenite, or oxidize ferrous
iron to ferric iron, or convert mercuric ion to elemental
mercury or the reverse. Various
enzyme
systems in living
organisms can biomethylate a number of heavy metals.
While it had been known for at least 60 years that arsenic
709
and selenium could be biomethylated,
microorganisms
ca-
pable of converting inorganic mercury into monomethyl and
dimethylmercury in lake sediments were not discovered until
1967. Since then, numerous heavy metals such as lead, tin,
cobalt, antimony, platinum, gold, tellurium, thallium, and
palladium have been shown to be biomethylated by bacteria
and
fungi
in the environment.
As environmental factors change the chemical reactivi-
ties and speciation of heavy metals, they influence not only
the mobilization, transport, and bioavailability, but also the
toxicity of heavy metal ions toward biota in both freshwater
and marine ecosystems. The factors affecting the toxicity
and
bioaccumulation
of heavy metals by aquatic organisms
include: 1) the chemical characteristics of the ion; 2) solution
conditions which affect the chemical form (speciation) of
the ion; 3) the nature of the response such as acute toxicity,
bioaccumulation, various types of
chronic effects
, etc.; 4)
the nature and condition of the aquatic animal such as age
or life stage, species, or
trophic level
in the food chain.
The extent to which most of the methylated metals are
bioaccumulated and/or biomagnified is limited by the chem-
ical and biological conditions and how readily the methylated
metal is metabolized by an organism. At present, only meth-
ylmercury seems to be sufficiently stable to bioaccumulate
to levels that can cause adverse effects in aquatic organisms.
All other methylated metal ions are produced in very small
concentrations and are degraded naturally faster than they
are bioaccumulated. Therefore, they do not biomagnify in
the food chain.
The largest proportion of heavy metals in water is
associated with suspended particles, which are ultimately
deposited in the bottom sediments where concentrations are
orders of magnitude higher than those in the overlying or
interstitial waters. The heavy metals associated with sus-
pended particulates or bottom sediments are complex mix-
tures of: 1) weathering and erosion residues such as iron and
aluminum
oxyhydroxides, clays and other aluminosilicates;
2) methylated and non-methylated forms in organic matter
such as living organisms, bacteria and algae,
detritus
and
humus
; 3) inorganic hydrous oxides and hydroxides,
phos-
phates
and silicates; and 4) diagenetically produced iron
and manganese oxyhydroxides in the upper layer of sedi-
ments and sulfides in the deeper, anoxic layers.
In anoxic waters the precipitation of sulfides may con-
trol the heavy metal concentrations in sediments while in
oxic waters adsorption,
absorption
, surface precipitation
and
coprecipitation
are usually the mechanisms by which
heavy metals are removed from the water column. Moreover,
physical, chemical and microbiological processes in the sedi-
ments often increase the concentrations of heavy metals in
the pore waters which are released to overlying waters by
diffusion or as the result of consolidation and bioturbation.