Lyme borreliosis in Europe: influences of climate and climate ...
Lyme borreliosis in Europe: influences of climate and climate ...
Lyme borreliosis in Europe: influences of climate and climate ...
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<strong>Lyme</strong> <strong>borreliosis</strong> <strong>in</strong> <strong>Europe</strong><br />
Page 15<br />
Climatic <strong>and</strong> environmental factors can affect LB risk <strong>in</strong> several ways by determ<strong>in</strong><strong>in</strong>g: the spatial<br />
tick distribution (at a range <strong>of</strong> scales from microhabitat to geographic region); daily variability <strong>in</strong><br />
risk <strong>of</strong> <strong>in</strong>fective tick bites; seasonal patterns <strong>in</strong> risk <strong>of</strong> <strong>in</strong>fective tick bites; <strong>in</strong>ter-annual variability<br />
<strong>in</strong> risk <strong>of</strong> <strong>in</strong>fective tick bites; <strong>and</strong> long-term trends.<br />
4.1. Climate <strong>and</strong> the life-cycle dynamics <strong>of</strong> the tick<br />
Both the length <strong>of</strong> each season as well as daily temperatures <strong>and</strong> humidity are important factors<br />
for the survival, development <strong>and</strong> activity <strong>of</strong> ticks. Ticks become active when the ambient<br />
temperature <strong>in</strong>creases above 4–5 °C, below which they are <strong>in</strong> a chill coma (Balashov, 1972;<br />
Duffy & Campbell, 1994; Clark, 1995). Higher temperatures are needed for metamorphosis <strong>and</strong><br />
egg hatch<strong>in</strong>g, i.e. between 8 ºC <strong>and</strong> 10–11 ºC respectively (Daniel, 1993).<br />
Average number <strong>of</strong> ticks per monitor routes<br />
90<br />
80<br />
80<br />
70<br />
60<br />
50<br />
40<br />
30<br />
20<br />
10<br />
0<br />
58<br />
11<br />
32<br />
36<br />
23<br />
27<br />
2<br />
I. ric<strong>in</strong>us<br />
I. persulcatus<br />
April May June July August September October<br />
Figure 4. Average seasonal activity <strong>of</strong> tick vectors <strong>in</strong> Latvia 1999–2002.<br />
Source: Kuulo Kutsar, 2004, personal communication.<br />
I. ric<strong>in</strong>us activity has a prom<strong>in</strong>ent annual cycle. Depend<strong>in</strong>g on location, ticks start to search for<br />
blood meals <strong>in</strong> early or late spr<strong>in</strong>g: <strong>in</strong> the Czech Republic this usually occurs <strong>in</strong> March or April,<br />
whereas <strong>in</strong> Latvia the start is later (Fig. 4). Both unimodal <strong>and</strong> bimodal (with peaks <strong>in</strong> both<br />
spr<strong>in</strong>g <strong>and</strong> autumn) seasonal tick activity peaks have been reported <strong>and</strong> seasonal occurrence <strong>of</strong><br />
the different tick stages may vary between years <strong>and</strong> regions (Nilsson, 1988; Mejlon & Jaenson,<br />
1993; Tällekl<strong>in</strong>t & Jaenson, 1997; Gray et al., 1998a; Zakovska, 2000; R<strong>and</strong>olph et al., 2002). In<br />
habitats where desiccation is common, such as open areas, periods <strong>of</strong> activity will be shortened<br />
to only a few weeks, as opposed to several months <strong>in</strong> dense woodl<strong>and</strong>s where moisture is higher<br />
(Gray, 1991).<br />
I. persulcatus behaves similarly to I. ric<strong>in</strong>us, except that autumn activity rarely occurs (Piesman<br />
& Gray, 1994; Korenberg 2000).<br />
The earlier the arrival <strong>of</strong> spr<strong>in</strong>g <strong>and</strong> the more extended the autumn season, the longer the period<br />
that allows ticks to be active <strong>and</strong> undergo metamorphosis. This may lead to a faster life-cycle<br />
with a reduction <strong>in</strong> the duration between tick bites (Balashov, 1972; Dobson & Carper, 1993). I.<br />
ric<strong>in</strong>us larvae <strong>and</strong> nymphs that feed <strong>in</strong> the early parts <strong>of</strong> the season moult <strong>in</strong>to the subsequent life<br />
stage <strong>in</strong> 1–3 months, whereas larvae <strong>and</strong> nymphs feed<strong>in</strong>g <strong>in</strong> the latter part <strong>of</strong> the season enter<br />
diapause, hibernate, <strong>and</strong> moult the follow<strong>in</strong>g year (Tällekl<strong>in</strong>t, 1996).<br />
31<br />
24<br />
7