dispersal of ticks and tick borne diseases by birds - Lista fuglestasjon
dispersal of ticks and tick borne diseases by birds - Lista fuglestasjon
dispersal of ticks and tick borne diseases by birds - Lista fuglestasjon
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order <strong>of</strong> magnitude (3-10 million<br />
imported nymphs per year). However,<br />
these are estimates with high<br />
uncertainties, <strong>and</strong> most <strong>of</strong> the<br />
uncertainties are due to the estimates <strong>of</strong><br />
bird populations. For example, nobody<br />
knows if the population <strong>of</strong> blackbird is<br />
closer to 200,000 or 2,000,000.<br />
Therefore, the uncertainty inherent in the<br />
method <strong>of</strong> sampling <strong><strong>tick</strong>s</strong> from <strong>birds</strong>,<br />
with the risk that some <strong>of</strong> the <strong><strong>tick</strong>s</strong> were<br />
acquired locally, will have a small<br />
impact on these calculations. Although<br />
the import <strong>of</strong> <strong>tick</strong> nymphs can be<br />
counted in millions, the number must be<br />
small compared to the number <strong>of</strong> <strong><strong>tick</strong>s</strong><br />
that actually exist in Norway. Therefore,<br />
the import <strong>of</strong> <strong><strong>tick</strong>s</strong> <strong>by</strong> <strong>birds</strong> would not<br />
have any mentionable effect on the<br />
population dynamics <strong>of</strong> an already<br />
existing population. In a long-term<br />
perspective, however, it could have an<br />
impact on the population genetics in<br />
places where migratory <strong>birds</strong> rest after<br />
crossing the Skagerrak. Unfortunately,<br />
the genetics tools that were developed<br />
for this purpose (Paper I) could not<br />
discriminate foreign from indigenous<br />
<strong>tick</strong> genes. As an I. ricinus female lays<br />
about 2000 eggs (R<strong>and</strong>olph 1998), the<br />
multiplication potential is enormous. If<br />
an imported <strong>tick</strong> brings genes that are in<br />
some way advantageous for the <strong><strong>tick</strong>s</strong>’<br />
survival, transport <strong>by</strong> <strong>birds</strong> might<br />
nevertheless have an impact on the gene<br />
pool <strong>of</strong> the population.<br />
From a quantitative point <strong>of</strong> view, other<br />
factors will be much more important<br />
than the <strong>birds</strong>’ import <strong>of</strong> <strong><strong>tick</strong>s</strong> <strong>and</strong> <strong>tick</strong><strong>borne</strong><br />
pathogens. The abundance <strong>of</strong> <strong><strong>tick</strong>s</strong><br />
in nature varies naturally from year to<br />
year, from site to site <strong>and</strong> with<br />
vegetation type (Stafford et al., 1995;<br />
Hubálek et al., 2003 b; Jouda et al.,<br />
2003; Wielinga et al., 2006). Vegetation<br />
type changes with changes in human use<br />
<strong>of</strong> the nature, <strong>and</strong> over the longer term,<br />
with climate. Cervid animals (moose, roe<br />
deer <strong>and</strong> red deer) have had a vastly<br />
increasing population in Norway over<br />
the last 50 years (Andersen et al., 2010).<br />
The distribution range <strong>of</strong> roe deer <strong>and</strong><br />
33<br />
red deer is still increasing, <strong>and</strong> mild winters<br />
may cause even more roe deer to survive.<br />
Apparently, the significance <strong>of</strong> cervid<br />
animals has increased dramatically since<br />
Thambs-Lyche made his great study on<br />
bovine babesiosis in the 1930s. Thambs-<br />
Lyche wrote: “roe deer hardly play any major<br />
role in the spreading <strong>of</strong> <strong><strong>tick</strong>s</strong>” <strong>and</strong>: “<strong><strong>tick</strong>s</strong><br />
have never been found on red deer”<br />
(Thambs-Lyche, 1943, pp 530 <strong>and</strong> 531).<br />
Now, hunters regularly find large numbers <strong>of</strong><br />
<strong><strong>tick</strong>s</strong> on these animals<br />
(http://www.flattogflue.no/). Ostfeld et al.<br />
(1998 <strong>and</strong> 2001) showed an interaction<br />
between masting <strong>of</strong> oak trees <strong>and</strong> the number<br />
<strong>of</strong> white-footed mice (Peromyscus leucopus),<br />
the behaviour <strong>of</strong> white-tailed deer<br />
(Odocoileus virginianus), who feed on<br />
acorns when available, <strong>and</strong> gypsy moths<br />
(Lymantria dispar). These moths feed on oak<br />
leaves <strong>and</strong> influence masting, while<br />
parasitoids regulate the population <strong>of</strong> gypsy<br />
moths, together with the white-footed mouse,<br />
which feed on the moths’ larvae <strong>and</strong> pupae.<br />
They found that the number <strong>of</strong> acorns<br />
influenced the number <strong>of</strong> mice, which in turn<br />
influenced the number <strong>of</strong> I. scapularis <strong><strong>tick</strong>s</strong><br />
(Ostfeld et al., 1998 <strong>and</strong> 2001). The indirect<br />
effect acorns had on the <strong>tick</strong> population was<br />
stronger than the effect <strong>of</strong> rainfall <strong>and</strong><br />
temperature found <strong>by</strong> Jones <strong>and</strong> Kitron<br />
(2000). The incidence <strong>of</strong> acute human cases<br />
<strong>of</strong> borreliosis is positively correlated with the<br />
abundance <strong>of</strong> questing <strong><strong>tick</strong>s</strong> (Stafford et al.,<br />
1998). This illustrates that the epidemiology<br />
<strong>of</strong> <strong>tick</strong>-<strong>borne</strong> <strong>diseases</strong> has to be viewed in a<br />
wide ecological framework, where climate is<br />
only one <strong>of</strong> the factors taken into account.<br />
Distribution ranges seem to be largely<br />
limited <strong>by</strong> vegetation <strong>and</strong> climate conditions,<br />
except in strictly host specific <strong><strong>tick</strong>s</strong>, like<br />
Amblyomma rhinocerotis, which is limited<br />
<strong>by</strong> the distribution <strong>of</strong> its rhinoceros hosts<br />
(Cumming, 1999). Vegetation can be studied<br />
with remote sensing (R<strong>and</strong>olph, 2000), using<br />
satellite data through the Normalised<br />
Difference Vegetation Index (NDVI), which<br />
basically measures the absorption <strong>and</strong><br />
reflection <strong>of</strong> red light <strong>and</strong> near infrared light<br />
to discriminate different vegetation types,<br />
such as scrub <strong>and</strong> grassl<strong>and</strong>, from forest.<br />
These data are obtained through the<br />
Advanced Very High Resolution Radiometer