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Chlorinated Dibenzofurans
Another group of halogenated hydrocarbons that has received
considerable attention in recent years because of the multiple
impacts of the contaminants on aquatic organisms includes the
chlorinated dibenzo-p-dioxins (CDDs) and chlorinated
dibenzofurans (CXDFs).
These aromatic heterocyclic compounds appear to be highly toxic
to marine organisms, and they can induce serious sublethal effects.
Occurring as trace contaminants in organic chemicals, such as
chlorinated phenols, PCBS, and phenoxy herbicides.
CDDs and CDfs enter estuarine and marine environments via
wastewater discharges, groundwater inflow, sewer overflows,
storms drains, and atmospheric deposition.
CDDS and CDFs are widely distributed in seawater and sediments
at low parts-per-trillion concentrations.
Being environmentally persistent and highly lipophilic compounds,
CCDs and CDFs tend to bioaccumulate in marine organisms by
food chain transfer rather than by direct uptake from seawater,
suspended matter, or bottom sediments.
2. Heavy Metals
b. Metal Toxicity
Heavy metals are toxic to marine organisms. The approximate
order of increasing toxicity of heavy metals, according to Abel,79
is a s follows: Co, Al, Cr, Pb, Ni, Zn, Cu, Cd, and Hg.
However, the toxicity of a given metal varies in estuarine and
marine organisms for several reasons :
(1) The capacity of the organisms to take up, store, remove, or
detoxify heavy metals differs considerably.
(2) Many intrinsic and extrinsic factors influence heavy metal uptake:
intra and inter-specifically variable intrinsic factors, such as
surface impermeability, nutritional state, stage of molt cycle, and
throughout of water by osmotic flux.
(3) Extrinsic physico-chemical factors, such as dissolved metal
concentration, temperature, salinity, presence or absence of
chelating agents, and presence or absence of other metals.
Once assimilated by marine organisms, heavy metals may be
sequestered by metallothioneins and lysosomes, thus facilitating
detoxification processes. Metal binding activity of metallothioneins
and lysosomes is also variable in marine organisms.
The toxicity of trace metals has been coupled to the free metal
ionic activity regardless of the total metal concentrations. In
marine environments, heavy metals occur in dissolved form (as
free ions, complexes ions, etc.) or in the solid state (as colloids,
adsorbed onto particle surfaces, in mineral matrices, etc.) They
may be present as inorganic and organic species.
At toxic levels, heavy metals act as enzyme inhibitors in marine
organisms. They also adverse affect cell membranes.
Organometallic species often damage reproductive and central
nervous systems.
Other disruptions include changes in physiology and development.
Feeding behavior, digestive efficiency, and respiratory metabolism
commonly are adversely affected.
a. Metal Concentration
i. Copper
The levels of copper in estuarine waters (-0.2 to > 100 g) are usually
much greater than those in oceanic waters (~0.1 g/1) because
dissolved copper sorbs to particulate matter, the concentrations in
bottom sediments can be a substantial. A positive correlation exists
between the concentrations of copper in sediments and those observed
in many benthic species.
ii. Cadmium
The concentrations of cadmium in coastal waters removed from
industrialized centers range from 1-100 ng/1. Where inputs are
elevated because of industrial or municipal waster disposal.
Cadium accumulates in bottom sediments at, cadmium
concentrations generally range from 0.1-10.0 g/g, dry wt.
Mussels (Mytilus spp.) used as sentinel organisms in coastal
regions have accumulated cadmium to mean levels of 1-5 g/g
dry wt.
iii. Lead
The concentrations of lead in the open ocean range from 0.001-
0.014 g/1. Lead levels in estuaries and coastal marine waters
exceed those in the open ocean by a factor of 10 or more.
Organ lead compounds are generally more toxic to marine
organisms than inorganic forms. The amount of lead in marine
mammals (i.e., dolphins, porpoises, seals, and whales) from
waters around the British Isles is 0.05 7.0 g/g wet wt.2
Mercury
7. Radioactivity
a. Sources
i. Natural Sources
Radionuclides in estuarine and marine environments derive from
both natural and anthropogenic sources (Tables 24-26).
Natural background radiation is attributable to cosmogenic and
primordial radionuclies.
Cosmogenic radionuclides originate from the interaction of
primary cosmic rays with matter in the atmosphere and on the
surface of the earth.
The collision of high energy particles (cosmic radiation) with
nitrogen, oxygen, argon, and other atoms in the upper atmosphere
produces secondary particles, primarily neutrons and protons.
Secondary cosmic radiation accounts for nearly all cosmic rays
impinging on the sea surface.
Primordial radio nuclides are those that were generated at the time
of formation of the earth.