Page 181 - Soil and water contamination, 2nd edition
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168                                                  Soil and Water Contamination

                    PAHs include (the number between brackets indicates the number of benzene rings, but note
                    that PAHs may also contain additional non-benzene rings): acenaphtene (2), acenaphthalene
                    (2), anthracene (6), benz[a]anthracene (4), benzo[b]fluoranthene (4), benzo[k]fluoranthene
                    (4), benzo[ghi]perylene (6), benzo[a]pyrene (5), chrysene (4), dibenz[a.h]anthracene (5),
                    fluorantene (3), fluorine (2), indeno[1.2.3-cd]pyrene (5), naphthalene (2), phenanthrene (3),
                    and pyrene (4).
                       PAHs  enter the atmosphere mostly as releases from volcanoes, forest and peat fires, fossil
                    fuels combustion, coke and asphalt production, waste incineration, and aluminium smelting.
                    In air, PAHs occur mostly attached to dust particles smaller than 1–2 μm. Over a period of
                    days to weeks, PAHs can break down by reacting with sunlight and other airborne chemicals.
                    They are also removed from the atmosphere by deposition, as a result of which they reach
                    the Earth’s surface. The lighter molecular weight  PAHs can be revolatilised and redistributed
                    before they are redeposited. Although PAH levels in air, soil, and water are particularly
                    enhanced in urbanised regions, PAHs are ubiquitous in the environment, even in remote
                    areas, due to long-range atmospheric transport. In addition to atmospheric deposition , the
                    sources of PAHs to terrestrial environments include releases from creosote-treated products,
                    spills of petroleum  products, and application of compost.
                       The PAH contents of terrestrial plants and animals may be substantially greater than the
                    PAH contents of soil on which they live, albeit that the PAH contents in terrestrial plants are
                    often independent from those in soil because PAH compounds are poorly soluble and poorly
                    available in soils (ATSDR, 2013). A major source of PAHs  in plants is the accumulation of
                    airborne PAHs on plant leaves; plant uptake  of PAHs via the root system is often negligible.
                    The process of accumulation is affected by a variety of factors. It increases with decreasing
                    ambient temperature, and with increasing leaf surface area and lipid concentration in plant
                    tissues. Volatile PAHs with a lower molecular weight  are primarily subject to dry gaseous
                    deposition, whereas non-volatile PAHs mainly accumulate on plant surfaces in the form of
                    dry particulates (Bakker, 2000). The volatile PAHs enter plants primarily through gaseous
                    diffusion via open stomata, although absorption by the waxy leaf surface accounts for a
                    portion of the total PAHs in tissues. The waxy surface of leaves intercepts both gaseous and
                    particle-bound PAHs. Because of their ability to intercept PAHs from the atmosphere, a wide
                    range of plant species, including lichens, mosses, algae, and trees have been used to evaluate
                    environmental accumulation of PAHs (e.g. Franzaring et al., 1992; Wegener et al., 1992).
                    Mosses are particularly effective filters due to their large surface area, their capacity to absorb
                    large organic molecules, and their ability to obtain water and nutrients from the air.
                       Surface water contamination by PAHs  can occur through runoff from contaminated soil
                    surfaces (particularly urban runoff ), and direct discharges from industrial and wastewater
                    treatment  plants. In general, most PAHs are not very mobile in soil and water, due to their
                    relatively low solubilities and strong affinity for organic particulate matter. As a consequence,
                    PAHs tend to partition into sediments and soils. PAH levels are usually much higher in
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                    sediments than in surface water, i.e. in the range of μg kg  (ppb) rather than ng kg  (ppt).
                       PAHs  are potentially hazardous to plants due to photo-enhanced toxicity  in the presence
                    of ultraviolet (UV) or other types of solar radiation  (Irwin  et al., 1998). PAHs are good
                    photosensitisers, forming biologically harmful excited or singlet-state oxygen  radicals .
                    Their toxic effects include chlorosis , inhibition of photosynthesis , and diminished biomass
                    accumulation. Soil contamination by PAHs may also inhibit root growth. PAH toxicity in
                    aquatic environments is mainly associated with the more soluble compounds, particularly
                    two-ring compounds such as the naphthalenes, and some heavier PAHs that affect aquatic
                    macrophytes, benthic aquatic invertebrates (i.e. invertebrates that live on the bed of a
                    water body), and fish. As a consequence, aquatic animals in the water will have a decreased
                    individual fitness and will not be able to develop through their life stages successfully and
                    reproduce effectively. Some PAH compounds, however, appear to stimulate reproduction,










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