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on the size of the eggs and the number of spawnings per season These distinctions are important because the impact of pollution on fecundity, and therefore future population size, will depend on the life history and reproductive cycle of the particular species of sh In addition, most teleosts are iteroparous, that is they spawn over several years The total number of eggs produced over a sh s life will, therefore, depend on the total number of eggs spawned in a breeding season and the reproductive longevity of the sh However, not all iteroparous sh spawn every year Some sh show non-annual and or irregular periodicity (Burton & Idler, 1987; Burton, 1991) Consequently, when looking at the long-term effects of low-level pollution on fecundity, it is important to distinguish between batch fecundity, breeding season fecundity and lifetime fecundity.

one of the splitters, in order to identify the guilty party, loss measurements out to each subscriber are needed. One clever scheme for accomplishing this from the OLT proposes to install a re ective ber Bragg grating (FBG) (Section 3.2.1) at each ONU, each such FBG having been tuned to a different signature wavelength. Tuning the OTDR to each subscriber s FBG wavelength then diagnoses attenuation to that subscriber [Merel]. The OTDR is a particularly effective instrument for uncovering pathologies of PON systems. It is capable of seeing any kind of distributed or discrete points of loss or re ection and spotting its location. Figure 4.18b shows the kind of trace that can be seen on such an instrument for the topology of Figure 4.18a. After each transmitted pulse (typically a few microseconds long), there is received a slowly declining ramp in the re ected signal due to the backward-traveling Rayleigh scattering. Any signi cant spatially compact loss, such as that from a connector pair, splice, or

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Within a species and an individual, fecundity can vary within and between spawning and seasons Fecundity can be affected by growth rate and nutritional status For example, winter ounder has been shown to have a nutritionally sensitive period for gametogenesis, and insuf cient energy reserves at this time cause it to switch off gonad development (Burton, 1994) Similar effects have been observed in the sea bass (Dicentrarchus labrax), in which the effect of food ration on oestrogen and VtG plasma levels, fecundity and larval survival were compared (Cerda et al, 1994) It may be possible, therefore, for low-level pollution to have no adverse effect on a sh but to still affect its survival at a population level, by knocking out its food supply, particularly at important times.

35.1 33 30.9 27.8 25.8 25.8 22.7 20.6 20.6 18.6 13.4 7.2 6.2 1 11.3

SMG 641/98. Main elements of these results were integrated immediately in the SMG2 speci cations (see e.g. SMG2 status report of February 1999.

Fish, like many vertebrates and invertebrates, can also exhibit atresia (oocyte degeneration) in response to a number of factors including poor nutritional state This can occur at any stage of development and will theoretically affect the number of oocytes that form mature eggs and, therefore, fecundity Atresia, however, appears to be relatively uncommon in sh held under optimal conditions (Tyler et al, 1990) The problem again may be in separating pollution effects on atresia from nutritional effects in natural populations A fecundity gene (FecB gene) has been identi ed as playing a role in determining fecundity in mammals (Braw-tal et al, 1993; Montgomery et al, 1994) It is likely that a similar genetic basis to fecundity exists in sh This gene appears to affect the plasma level of the gonadotropin FSH and elevated plasma levels of this are associated with higher fecundity (McNatty et al, 1994).

2004, Taskar et al 2004, Roos et al 2005, Niculescu et al 2006, Tsamardinos et al 2006, Jakulin and Rish 2006, Castillo 2008]) This success does not come as a surprise: graphical models have several advantages when applied to knowledge discovery and data mining problems In the first place, as already pointed out, the network representation provides a comprehensible qualitative (network structure) and quantitative description (associated distribution functions) of the domain under consideration, so that the learning result can be checked for plausibility against the intuition of human experts Secondly, learning algorithms for inference networks can fairly easily be extended to incorporate the background knowledge of human experts In the simplest case a human domain expert specifies the dependence structure of the domain to be modeled and automatic learning is used only to determine the distribution functions from a database of sample cases.