Collecting faeces is viewed as a potentially efficient way to sample elusive animals. Nonetheless, any biases in estimates of population composition associated with such sampling remain uncharacterized. The goal of this study was to compare estimates of genetic composition and sex ratio derived from Eurasian otter Lutra lutra spraints (faeces) with estimates derived from carcasses. Twenty per cent of 426 wild-collected spraints from SW England yielded composite genotypes for 7-9 microsatellites and the SRY gene. The expected number of incorrect spraint genotypes was negligible, given the proportions of allele dropout and false allele detection estimated using paired blood and spraint samples of three captive otters. Fifty-two different spraint genotypes were detected and compared with genotypes of 70 otter carcasses from the same area. Carcass and spraint genotypes did not differ significantly in mean number of alleles, mean unbiased heterozygosity or sex ratio, although statistical power to detect all but large differences in sex ratio was low. The genetic compositions of carcass and spraint genotypes were very similar according to confidence intervals of theta and two methods for assigning composite genotypes to groups. A distinct group of approximately 11 carcass and spraint genotypes was detected using the latter methods. The results suggest that spraints can yield unbiased estimates of population genetic composition and sex ratio.

2004. Competition between Eurasian otter Lutra lutra and American mink Mustela vison probed by niche shift. Á/ Oikos 106: 19 Á/26.Interspecific competition is one of several constraints that might prevent an individual from maximising its energy intake. When an interspecific competitor is introduced, an individual is often forced to shift its diet according to the intensity of the competitive pressure. In this paper, we explore whether the introduced American mink (Mustela vison Schreber) shifts its diet when the density of its potential competitor, the Eurasian otter (Lutra lutra L.), is increased. We compared the diets of otter and mink at the same location but at two moments in time when the relative densities of these two species were different while controlling for the abundance of aquatic prey. Mink and otters are semi-aquatic mammals belonging to the same guild of mustelids and otters are expected to be the dominant competitor because they are larger and better at hunting underwater. The diets of otters and mink overlap to a great extent but while otters specialise mainly on aquatic prey, mink are able to exploit both aquatic and terrestrial prey. These observations prompted the hypothesis investigated in this work that at higher otter densities the diet of mink should change to include a higher proportion of terrestrial items. This hypothesis was supported by the data and at higher otter densities mink diet was observed to consist of a higher proportion of mammals and birds while fewer fish were present, although this pattern was present only in winter while no changes were observed in spring. Meanwhile the diet of otters remained basically unchanged. In the second part of the study, we investigated whether niche breadth and niche overlap between otter and mink changed at different otter densities. We found that niche overlap declined as the density of otters increased, in agreement with the prediction of habitat selection theory.

The results of analysing otter spraints from an eutrophic lake and an oligotrophic stream are described and compared with the results of a study of the mink's diet in the same areas. Differences between the otter's diets in the two areas are explained in terms of availability, and seasonal variation can be linked with changes in fish activity and behaviour. The mink takes a smaller proportion of fish in its diet than the otter, but there is considerable overlap and the min'k takes most species of fish eaten by the otter. On the lake, some differences in fish and bird predation can be detected and these may be connected with differences in the hunting behaviour of the predators. Food is abundant in this area and competition for it unlikely. On the river, the pattern of predation of fish by the two species is almost identical, the biomass of fish is low and waterside birds absent, conditions which could lead to competition.

Small, 1st and 2nd-order, headwater streams and ponds play essential roles in providing natural flood control, trapping sediments and contaminants, retaining nutrients, and maintaining biological diversity, which extend into downstream reaches, lakes and estuaries. However, the large geographic extent and high connectivity of these small water bodies with the surrounding terrestrial ecosystem makes them particularly vulnerable to growing land-use pressures and environmental change. The greatest pressure on the physical processes in these waters has been their extension and modification for agricultural and forestry drainage, resulting in highly modified discharge and temperature regimes that have implications for flood and drought control further downstream. The extensive length of the small stream network exposes rivers to a wide range of inputs, including nutrients, pesticides, heavy metals, sediment and emerging contaminants. Small water bodies have also been affected by invasions of non-native species, which along with the physical and chemical pressures, have affected most groups of organisms with consequent implications for the wider biodiversity within the catchment. Reducing the impacts and restoring the natural ecosystem function of these water bodies requires a three-tiered approach based on: restoration of channel hydromorphological dynamics; restoration and management of the riparian zone; and management of activities in the wider catchment that have both point-source and diffuse impacts. Such activities are expensive and so emphasis must be placed on integrated programmes that provide multiple benefits. Practical options need to be promoted through legislative regulation, financial incentives, markets for resource services and voluntary codes and actions.

The records of one pack of Otter Hounds hunting in southwest England are examined for the prriod 1907 to 197 1 as well as the records of all packs active in Britain between 1950 and 1976. The hunting success per unit effort varies from year to year depending o n changes in hunting conditions but longer term changes can also be identified. The hunting success of the Culmstock Otter Hounds (hunting in parts of south-west England) increased steadily from 1907 to 1956 but in most of England and south Wales the success rate of the hunts declined rapidly after 1957. There was also a tlrcline in success in northern England and southern Scotland but to a lesser extent, while in north Walra and Eire, there is no evidence for a decline.'fhese changes are considered to reflect changes in otter populations but the extent of the decline in hunting success (to between 37% and 55% of previous levels in the southern hunts) is probably less than the actual decline in otter numbers. There are no signs of a recovery in the population but indications o f a continuing decline up to 1976.The reason for the increasing population in the first half of the century in south-west England is p~-obably the decrease in persecution since the nineteenth century. A variety of causes for the crash in thr late 1950s are considered and the factor most likely to be responsible is the introduction of the dieldrin group of insecticides in 1956. Use of these compounds has been increasingly restricted since 11163 and the possible reasons for the failul'e of the otter population to recover are listed but no firm conclusions can be drawn as yet.