Tick-borne viruses in Europe. A main determinant of the numbers of rodents is the availability of nutrients, which is partly related to the production masting of fruits of oak, beech, chestnut and other trees [ 24 ]. A reason for a life-cycle shorter than three years could be that the microclimate in the densely tick-infested biotopes and in particular in the TBEV foci of southern Sweden, are in general warmer than the surrounding environment [ 22 , ]. Thus, more roe deer in south-western and southern Sweden increased the number of TBEV foci, which increased the risk for people in these regions to become infected with TBEV. The covariance was positive in five of the regions and clearly significant in three Fig.

vildsvinsfeber 2

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vildsvinsfeber 2

Forest structure and roe deer abundance predict tick-borne encephalitis risk in Italy. Thus, when deer abundance vildsvisnfeber from a high level the result may be an increased incidence of human TBE [ 40].

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Important investigations on the relationships between deer abundance and climatic factors as determinants of I. Similarly, in the USA Ostfeld and co-workers [ 9394 ] found that the risk for people to become exposed to I.

Wild deer as a source of infection for livestock and humans in the UK. Commissioner Andriukaitis also underlined that it is crucial that every single hunter is aware and pays attention to how easily the disease can spread.

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Secondly, in southern Sweden an unknown proportion of the nymphs may possibly be younger than two years. It could be that occasionally small TBEV foci are formed in a manner similar to that by which some foci of another Vildsvinsfeerthe Kyasanur Forest disease virus KFDV foci are thought to arise []: A warmer winter climate may additionally be beneficial to the tick hosts and for the ticks themselves, and could therefore increase the potential bildsvinsfeber TBEV transmission.

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Likewise, the temperature sums were square-root-transformed. The role of large herbivores in Ixodes ricinus and Borrelia burgdorferi s. Most or all of these migrating young roe deer were presumably, during most of the year, tick-infested.

Rodents as hosts for Ixodes ricinus and Borrelia afzelii. Field evidence that roe deer Capreolus capreolus are a natural host for Ehrlichia phagocytophila.

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Sequencing of a tick-borne encephalitis virus from Ixodes ricinus reveals a thermosensitive RNA vildsvlnsfeber significant for virus propagation in ectothermic arthropods. Lindstrom A, Jaenson TG. Changes in the geographical distribution and abundance of the tick Ixodes ricinus during the past 30 years in Sweden.

vildsvinsfeber 2

Accessed 30 Nov These examples show that the function of roe deer as an important tick maintenance host can be replaced by other ungulates and even by hares. This means that most of the increase in temperature sum took place between and Temperature readings were taken every third hour from 1st January to 31st July at four different localities Fig. All monthly indices for that year were then added to create an annual temperature sum. Another factor to realise is that if the density of deer decreases the availability of potential hosts to host-seeking ticks is consequently reduced.

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Daniels TJ, Fish D. Climate and environmental change drives Ixodes ricinus geographical expansion at the northern range margin.

vildsvinsfeber 2

The density of I. Petersson2 David G. The role of deer as vehicles to move ticks, Ixodes ricinusbetween contrasting habitats. Population regulation in ticks: Open in a separate window. This article has been cited by other articles in PMC.

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The de-trended standardised values for roe deer abundance versus incidence of TBE are shown in Fig. The end of the vegetation period is calculated in a corresponding manner, i. Associated Data Supplementary Materials Additional file 1: Continuing increase of tick bites and Lyme disease between and Indirectly, deer are important tick producers since they feed large numbers of adult ticks [ 25 ]. Based on a seven-year long field study in France, Paul et al.