Page 307 - Soil and water contamination, 2nd edition
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294                                                  Soil and Water Contamination

                    resulting concentration patterns of the heavy metals Zn, Cd, and Pb in the topsoil in the
                    vicinity of the incinerator. The heavy metals  have dispersed predominantly north-eastwards,
                    due to the prevailing south-western winds. The maximum concentrations of heavy metals
                    occur at a distance from 1.5 to 2.0 kilometres away from the incinerator, where the plume
                    from the chimney most often reaches the soil surface. It is conspicuous that the maximum
                    concentrations do not coincide for the different metals. The maximum levels of Cd are found
                    nearer the source than Zn and Pb. This is probably due to different transport ranges of the
                    different particle size fractions to which the metals bind. Zinc and lead vaporise during
                    incineration and condense mainly onto the smallest airborne particles that have the largest
                    specific surface. Cadmium does not vaporise and, as a consequence, remains also associated
                    to the somewhat larger particle fractions. These larger particles are transported over shorter
                    distances than the smaller particles (De Fré et al., 1992).
                       At the local scale, deposition is affected by aerodynamic surface roughness  controlled
                    by local surface topography and land cover (Bachhuber  et al., 1987; Draaijers, 1993).
                    The presence of hills and transitions in the height and structure of vegetation cover causes
                    airflow perturbations which alter the rates of dry and wet atmospheric deposition . Draaijers
                    (1993) studied the effect of canopy and forest edge structure on deposition amounts in the
                    Netherlands, using the so-called throughfall  method. Throughfall refers to the precipitation
                    water dripping from the leaves, needles or branches and falling through the canopy gaps.
                    By measuring the amount and composition of the throughfall water using gutters of 5 m
                                                       2
                    long and a total collection area of 0.054 m , the total deposition (i.e. wet + dry + occult
                    deposition ) flux could be estimated. Strong correlations were found between net throughfall
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                    fluxes of SO , NO , NH , Na , and Cl  and the roughness and leaf area of forest canopies.
                             4     3    4
                    Draaijers (1993) also observed an exponential increase of the net through fluxes towards the
                    forest edge, although there was a considerable scatter around this general trend (Figure 16.7).
                    Because the sample support  (i.e. gutter length) was of the same order of magnitude of one
                    tree crown, this scatter was largely attributed to short-range variability associated with the
                    leaf area and the occurrence of branches and canopy gaps above the gutters. The width of the
                    zone with enhanced net throughfall fluxes approximated 5 edge heights. The net throughfall
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                                2-
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                    increase of SO , NO , NH  near the forest edges (on average, a factor of 2) was smaller
                               4     3     4
                                        -
                                 +
                    than that of Na  and Cl  (on average, a factor of 5). These differences were attributed to
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                                                                                     2-
                    the sources for these ions in throughfall. In the Netherlands, net throughfall of SO , NO ,
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                                                                                     4
                        +
                    NH  occurs predominantly through dry deposition  of gases and particles smaller than 1 μm,
                       4
                                           +
                                                  -
                    whereas net throughfall of Na  and Cl  mostly occurs by dry deposition of sea salt particles
                    larger than 1 μm. In the Draaijers study, differences between forests in net throughfall
                    increase in forest edges were attributed to differences in forest density and edge aspect. Net
                    throughfall fluxed was found to be positively correlated to forest density; forest edges exposed
                    to prevailing wind directions (south and south-west) exhibited enhanced dry deposition.
                       Draaijers et al. (1994) and Weathers et al. (2001) have discussed the relevance of these
                    forest edge effects for atmospheric deposition  in complex and patchy forested landscapes. As
                    forest edges can function as significant traps both for airborne nutrients and for pollutants
                    from adjacent agricultural  or urban landscapes, an important factor in quantifying
                    contaminant inputs to the soil surface through atmospheric deposition is the landscape
                    structure and fragmentation. In the Netherlands, almost 80 percent of all forest complexes
                    are smaller than 5 ha, and more than 70 percent of all individual forest stands are smaller
                    than 1.5 ha. Assuming a forest edge of five edge heights, at least 50 percent of the total forest
                    area in the Netherlands is affected by edge effects (Draaijers, 1993).
                       The atmospheric deposition of acidifying components (NO , NH , SO ) has not only
                                                                      x    3    2
                    caused soil pH to fall, but has also caused secondary pollution through the loss of Ca
                    from the soil profile and the mobilisation of toxic aluminium. These effects are especially
                    noticeable in poorly buffered soils that are low in bicarbonate, soil organic matter, cation
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