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To prove the ultrametric inequality, let x, y, z S and suppose that d(x, y) = p, d(x, z) = q, and d(z, y) = r There exist H, K, L H such that {x, y} H, h(H) = p, {x, z} K, h(K) = q, and {z, y} L, h(L) = r Since K L = (because both sets contain z), we have either K L or L K, so K L equals either K or L, and in either case, K L H Since {x, y} K L, it follows that d(x, y) h(K L) = max{h(K), H(L)} = max{d(x, z), d(z, y)}, which is the ultrametric inequality We refer to the ultrametric d whose existence is shown in Theorem 8 as the ultrametric generated by the graded hierarchy (H, h).

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1991; Poulet et al, 1994) It is not yet clear whether infectious agents are involved in the development of epidermal papillomas, but viral particles have been recorded from these lesions in some sh species (see Baumann, 1992; Grizzle & Goodwin, 1998) Cellular changes in the integument predominantly affect the epithelial layers of the skin and if the stimulant persists, more severe lesions may occur affecting deeper tissues, including the underlying musculature (Bucke et al, 1983; Lindesj & Thulin, 1994) Additional pathologies of the integument include cellular hypertrophy, necrosis, erosion and sloughing of the epidermis (including n rot) (Haensly et al, 1982), and proliferation of mucous cells or changes in their relative abundance Hyperplasia of pigment cells (melanocytes and iridophores) leading to hyperpigmentation has been recorded in some at sh species, such as the dab (Limanda limanda), from the North Sea.

where w1 (k + 1) = + + 1)||. Alternatively, we can use the ordered rotation KuicNet learning rule proposed recently by S. Douglas and S. Y. Kung [415]

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Example 6 The values of the ultrametric generated by the graded hierarchy (H, h) on the set S, introduced in Example 5, are given in the following table d s t u v w x y s 0 3 3 5 7 7 7 t 3 0 3 5 7 7 7 u 3 3 0 5 7 7 7 v w 5 7 5 7 5 7 0 7 7 0 7 4 7 6 x 7 7 7 7 4 0 6 y 7 7 7 7 6 6 0.

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The occurrence of this condition has been increasingly noted Histological examination of affected tissues has so far failed to demonstrate evidence of pathogen involvement and the aetiology of the condition remains unknown (Lang & Feist, unpublished) With the exception of papillomas, cutaneous neoplasms, including carcinomas, are relatively rare However, Baumann (1992) suggested that chromatophoromas in certain sh species may be of use in environmental monitoring Further, Kranz (1989) identi ed relationships between ulcers of the skin and melanomacrophage (MMC) centres in the spleen There are no known direct links between xenobiotic exposure and pathologies of the integument, although exposure to xenobiotics could affect the progress of skin and integument pathologies If the ability of the immune system of a sh to combat pathogens is compromised, eg through effects of xenobiotics on either humoral or cellular immune system components (see section 4.

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# Calculate M(s) (w12*w23*w34)/(1-(w12*w21)-(w23*w32)); end proc; # Make the MGF mx := makeproc(ms(s),[s]):

2), one obvious consequence could be slower healing of skin ulcerations Similarly, effects of xenobiotics on blood clotting could delay healing processes in integument..

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