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Organic pollutants                                                    169

                   which suggest they have an oestrogen-like action. Microorganisms can break down PAHs in
                   soil or water after a period of weeks to months, though some PAHs are resistant to decay.
                   Microorganisms degrade low molecular weight  PAHs more easily than higher molecular
                   weight PAHs. Non-substituted PAHs will also be degraded faster than alkyl-substituted
                   PAHs (Lundstedt et al., 2003).
                      With respect to humans, PAHs  are generally associated with chronic risks, which are
                   often the result of exposure to complex mixtures of aromatic  compounds rather than to low
                   levels of a single compound. Toxic effects include DNA adducts and cancer. In general, the
                   heavier (4-, 5-, and 6-ring) PAHs have greater carcinogenic potential than the lighter (2-
                   and 3-ring) PAHs (ATSDR, 2013). Human exposure to PAHs is mainly via the inhalation
                   of contaminated air in the work environment and outdoors, and the ingestion of grilled or
                   charred meats or contaminated water, cow’s milk, or other foodstuffs (e.g. cereals, vegetables,
                   fruits).


                   9.5  CHLORINATED HYDROCARBONS

                   Chlorinated hydrocarbons, also known as organochlorins , are hydrocarbons with one or
                   more chlorine substituents. These compounds can consist of aliphatic  as well as aromatic
                   structures, and include a wide range of compounds. The carbon–chlorine bond is strong and
                   makes organochlorins very stable. Because of this property, many chlorinated hydrocarbon
                   compounds have been synthesised and used extensively in agricultural and industrial
                   applications. In particular, the use of organochlorins as pesticides  has resulted in a widespread
                   contamination of aquatic and soil systems. Chlorinated hydrocarbons that are pesticides
                   include DDT , aldrin , dieldrin , heptachlor, chlordane, lindane, endrin, and hexachloride.
                   The chemical structures of these compounds are depicted in Figure 9.1. Other sources of
                   environmental contamination by chlorinated hydrocarbons include spills from chemical
                   facilities, improper disposal or leakage from storage containers or waste sites, and the burning
                   of waste containing plastics, especially polyvinylchloride (PVC ).
                      Because organochlorins  are very stable, these molecules tend to persist in the
                   environment for a long time and biomagnify in the food chain. Chlorinated hydrocarbon
                   compounds are very toxic to fish and invertebrates, as well as to any other animals that may
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                   feed on them. The 96-hour LC50  for tested animals ranges from 1–60 μg l , depending
                   on the species. To account for their great bioaccumulation  and biomagnification  potential,
                   the US Environmental Protection Agency has stipulated that the amount of chlorinated
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                   hydrocarbon compounds permitted in the water must not exceed 0.001 μg l . However,
                   even at low chronic doses, these compounds have the potential to cause problems, including
                   hormone disruption leading to reduced reproductive success and damage to the central
                   nervous system. In humans, they may also cause liver and kidney damage. Because of their
                   persistence, tendency to bioaccumulate, and toxicity  to non-target species, most chlorinated
                   hydrocarbon pesticide uses have been phased out in the developed countries.












                   Figure 9.1  Examples of some organochlorine pesticides.









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