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6 Wood Discoloration

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182 8 Habitat of <strong>Wood</strong> Fungi<br />

The type and intensity of a biological attack can be recognized by different<br />

macromorphologic changes of the wood tissue. Typical discolorations occur<br />

on and inside wood that is colonized by molds, blue stain, and red-streaking<br />

fungi. Brown- and soft-rotten woods differ in color and shape of the brown<br />

and soft-rotten cubes, and white-rotten wood between simultaneous and white<br />

pocket rot.<br />

Various mechanical and physical wood changes occur when wood-inhabiting<br />

microorganisms colonize wood. <strong>Wood</strong> mass (weight) loss is a commonly<br />

used measure of decay capability. The basic calculation is: [(weight before −<br />

weight after): weight before] ×100%. The extent of decay in a specimen that<br />

was sampled from attacked wood can be determined the same way, if its dry<br />

weight is compared to that of a comparable healthy control: mass loss ML<br />

(%) = [(DW1 −DW2) :DW1] × 100 (DW1 = dry weight of control, DW2 =dry<br />

weight of decayed sample).<br />

Mass loss of wood samples exposed to fungi is likewise used to determine the<br />

efficacy of wood preservatives and to examine the natural durability of wood<br />

species. There is a permanent discussion if fungal pure cultures or artificial<br />

mixed cultures should be used in laboratory tests (Kolle flask method, soilblock<br />

test, vermiculite method) or if soil contact decay tests are preferable.<br />

Laboratory tests are reproducible as they are based on defined test fungi.<br />

Field stake tests result in a severe exposure condition as the natural microbial<br />

composition may contain microorganisms that degrade wood, biodegrade<br />

organic wood preservatives or modify inorganic preservatives making them<br />

more susceptible to leaching (Nicholas and Crawford 2003). In Europe, the<br />

Kolle flasks method with malt extract agar and defined wood blocks of 5 ×<br />

2.5 × 1.5 cm in size from Scots pine sapwood and European beech is used for<br />

Basidiomycetes according to the standard EN 113 (Fig. 7.5; Table 7.6). In this<br />

method, specified isolates of certain fungal species, e.g., Coniophora puteana<br />

Ebw. 15, have to be used. The wood decay capacity of the test organisms is,<br />

however, erroneously named “virulence”, although it concerns fungi and not<br />

viruses.Soft-rotfungi tests are performedinplasticcontainers with vermiculite<br />

(grainy substance of aluminum iron magnesium silicate) as moisture and<br />

nutrient depot. The standard soil block test AWPA E10 uses either 14-mm or<br />

19-mm wood cubes that are exposed to white- and brown-rot fungi that were<br />

previously inoculated onto wood wafers on top of a sterile moist soil bed in<br />

a bottle. Soil bed testing based on the methodology described in the European<br />

Pre-standard ENV 807 uses 100 mmlong ×10mmrad ×5mmtang specimens that<br />

are exposed to the naturally soil-inhabiting microorganisms (v. Acker et al.<br />

2003). Field stake tests use stakes or posts of the selected wood species that<br />

are half buried vertically in soil and inspected for decay at intervals. <strong>Wood</strong><br />

assembly above-ground tests (post-rail, L-joint, lap-joint), all including some<br />

type of joint that effectively traps rainwater, simulate decking, door frames or<br />

joinery (Zabel and Morrell 1992; Nicholas and Crawford 2003).<br />

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