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Lough Gur Environmental Management Study February 2009

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As a result on-site treatment systems have been implicated as a source of pollution in some lakes<br />

where dwellings are located nearby (DEHLG, 2000 and Moran, 2003) although the evidence suggests<br />

that a significant amount of DWE phosphorus is immobilised in the vadose zone sediments (Zanini et<br />

al., 1998).<br />

Phosphorus is mainly present in the DWE as orthophosphate, dehydrated orthophosphate and<br />

organic phosphorus (Siegrist et al., 2000). Bouma (1979) reported on studies that found that more<br />

than 85% of total phosphorus in the DWE was in the soluble orthophosphate form. The organic<br />

phosphorus in the effluent can be subject to mineralisation, in a way similar to organic nitrogen,<br />

resulting in the production of soluble inorganic phosphate (Brady and Weil, 2002). Phosphate is<br />

generally immobilised within a few metres of the percolation trench and significant movement of<br />

phosphate is rare (Reneau et al., 1989). As a result contamination of groundwater with phosphorus<br />

is seldom investigated or reported. However, studies have identified phosphorus leaching in areas<br />

with sandy soil, shallow water tables and in phosphorus saturated soils (Breeuwsma et al., 1995).<br />

Phosphorus attenuation in the subsurface is controlled by soil absorption and mineral precipitation<br />

reactions which can be considered in two general categories: initial absorption reactions and much<br />

slower precipitation reactions that regenerate additional absorptive surfaces occurring both from<br />

phosphate in solution and from phosphate previously absorbed (Lance, 1984).<br />

The types of reaction that fix phosphorus in relatively unavailable forms differ from soil to soil and<br />

are closely related to soil pH. In acid soils these reactions involve mostly Al, Fe or Mn, either as<br />

dissolved ions, as oxides, or as hydrous oxides. In alkaline and calcareous soils the reactions<br />

primarily involve precipitation as various calcium phosphate minerals or adsorption to the iron<br />

impurities on the surfaces of carbonates and clays. At moderate pH values, adsorption on the edges<br />

of kaolinite or on the iron oxide coating on kaolinite clays plays an important role (Brady and Weil,<br />

2002). Arias et al., (2001) report that at pH levels greater than 6 the reactions are a combination of<br />

physical adsorption to Fe and Al oxides and precipitation as sparingly soluble calcium phosphates. At<br />

lower pH levels they suggest that precipitation as Fe and Al phosphates becomes increasingly<br />

important. It is clear, therefore, that the capacity of a subsoil to fix phosphate is dependent on the<br />

presence of Fe, Al, Mn and Ca. Robertson (2001) found that the organic matter in DWE causes iron<br />

in soils to become soluble. As a result the phosphorus is precipitated out of solution forming a stable<br />

coating on the soil particles.<br />

Results of Phase 1 Survey of On-Site Treatment Systems<br />

From the <strong>Lough</strong> <strong>Gur</strong> survey map 19 no. houses, from H14 to H33 inclusive, were selected for<br />

assessment of their on-site treatment system under Phase 1 of the project. Field work revealed 2 no.<br />

of these to be derelict while 1 no. did not exist (H21). Of the remaining 16 no. houses it was not<br />

possible to gain access to 3 no. of them as the residents were absent from 2 no. of them and<br />

admission to the third was refused. It was agreed with Mr. Barry Murphy that these houses would be<br />

surveyed during a future phase, where possible. Therefore, 13 no. on-site systems were inspected in<br />

total and 12 no. samples of wastewater effluent collected and send to BHP Laboratories, Limerick for<br />

analysis. There was no wastewater effluent present in 1 no. of the systems inspected (H25).<br />

<strong>Lough</strong> <strong>Gur</strong> E nvironmental <strong>Management</strong> <strong>Study</strong>

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