A person who keeps or controls a dog in his own interest is liable "without fault" should that dog cause harm to any person. By owning a dog, man welcomes into his home a beast that preserves much of its primordial self, and is capable of inflicting a fatal bite wound. The courts may require the forensic expert to identify which specific dog caused the damage or fatal bite in an effort to establish the owner/controller of the animal. Very little has been published on the individualisation of dog bite marks, the procedures to be followed when confronted with usable bite marks and the range of analysis techniques available. The authors advocate a multidisciplinary approach, and utilise a case study to demonstrate the protocol to be followed when analysing a dog bite mark. The paper also highlights differences between human and dog inflicted bites. The authors warn against over interpretation of poor quality bite marks and a final conclusion of absolute certainty.

Trade‐offs between moult and fuelling in migrant birds vary with migration distance and the environmental conditions they encounter. We compared wing moult and fuelling at the northern and southern ends of migration in two populations of adult Common Whitethroats Sylvia communis. The western population moults most remiges at the breeding grounds in Europe (e.g. Poland) and migrates 4000–5000 km to western Africa (e.g. Nigeria). The eastern population moults all remiges at the non‐breeding grounds and migrates 7000–10 000 km from western Asia (e.g. southwestern Siberia) to eastern and southern Africa. We tested the hypotheses that: (1) Whitethroats moult their wing feathers slowly in South Africa, where they face fewer time constraints than in Poland, and (2) fuelling is slower when it coincides with moulting (Poland, South Africa) than when it occurs alone (Siberia, Nigeria). We estimated moult timing of primaries, secondaries and tertials from moult records of Polish and South African Whitethroats ringed in 1987–2017 and determined fuelling patterns from the body mass of Whitethroats ringed in all four regions. The western population moulted wing feathers in Poland over 55 days (2 July–26 August) at a varying rate, up to 13 feathers simultaneously, but fuelled slowly until departure in August–mid‐September. In Nigeria, during the drier period of mid‐February–March they fuelled slowly, but the fuelling rate increased three‐fold in April–May after the rains before mid‐April–May departure. The eastern population did not moult in Siberia but fuelled three times faster before mid‐July–early August departure than did the western birds moulting in Poland. In South Africa, the Whitethroats moulted over 57 days (2 January–28 February) at a constant rate of up to nine feathers simultaneously and fuelled slowly from mid‐December until mid‐April–May departure. These results suggest the two populations use contrasting strategies to capitalize on food supplies before departure from breeding and non‐breeding grounds.

Climate change appears to affect body size of animals whose optimal size in part depends on temperature. However, attribution of observed body size changes to climate change requires an understanding of the selective pressures acting on body size under different temperatures. We examined the link between temperature and body mass in a population of mountain wagtails (Motacilla clara) in KwaZulu-Natal, South Africa, between 1976 and1999, where temperature increased by 0.18 • C. The wagtails became lighter by 0.035g per year. Partitioning this trend, we found that only a quarter of the effect (0.009g / year) was due to individuals losing weight and three quarters (0.027g / year) was due to lighter individuals replacing heavier ones. Only the latter component was statistically significant. Apparently, the wagtails were reacting to selection for reduced weight. Examining survival, we found that selection was temperaturemediated, i.e. lighter individuals survived better under high temperatures whereas heavier individuals survived better under low temperatures. Our results thus support the hypothesis that temperature drove the decline in body mass in this wagtail population and provides one of the first demonstrations of the selective forces underlying such trends.

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Little is known about the louse species harboured by Red-footed and Amur Falcons despite the fact that various life-history traits of these hosts make them good model species to study host-parasite interactions. We collected lice samples from fully grown Amur (n=20) and Red-footed Falcons (n=59), and from nestlings of Red-footed Falcons (n=179) in four countries: Hungary, India, Italy and South Africa. We identified 3 louse species on both host species, namely Degeeriella rufa, Colpocephalum subzerafae and Laembothrion tinnunculi. The latter species has never been found on these hosts. Comparing population parameters of lice between hosts we found significantly higher prevalence levels of D. rufa and C. subzerafae on Amur Falcons. Adult Red-footed Falcons had higher D. rufa prevalence compared to C. subzerafae. For the first time we also show inter-annual shift in prevalence and intensity levels of these species on Red-footed Falcons; in 2012 on adult hosts C. subzerafae had higher intensity levels than D. rufa, however in 2014 D. rufa had significantly higher intensity compared to C. subzerafae. In case of nestlings both louse species had significantly higher preva lence levels than in 2014. The exact causes of such inter-annual shifts are yet to be understood.