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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

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