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Ecole Nationale Supérieure Agronomique de Montpellier ... - CIAM

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MATERIALS AND METHODS<br />

Characteristics of the Group of Orchards<br />

The 4 contiguous plots, planted in 1982, are located in the Rhone Valley near the city of<br />

Valréas (Vaucluse, France). They are quite isolated from other orchards (the closest one is<br />

about 3 km away). Their size ranges from 68 to 596 trees, and the planting distance is 5 m<br />

within and across rows. Each orchard was planted with a different combination<br />

rootstock/cultivar. Three apricot cultivars (‘Polonais’, ‘Rouge <strong>de</strong> Fournès’ and ‘Mo<strong>de</strong>sto’),<br />

and four rootstocks were used: myrobalan (P. cerasifera), GF 8-1 (P. marianna), GF 31<br />

(P. cerasifera × P. salicina) and P. armeniaca ‘Manicot’ (for more <strong>de</strong>tails, see Fig. 1A).<br />

Symptomatic trees were not removed. Most of them died within about 2 years. Before 1993,<br />

<strong>de</strong>ad trees were replaced; after this year, they were just cut.<br />

Disease Assessment<br />

From March 1984 to March 2000, this group of orchards was inspected twice a year (in<br />

March and October). The trees with typical ESFY symptoms (early bud break, paper-like<br />

rolled leaves, off-season growth) were located on a map. The trees with new symptoms in<br />

March were pooled with those recor<strong>de</strong>d in October the year before, because the vectors live<br />

on Prunus from March to July (Labonne and Lichou, 2003). Replanted trees were not taken<br />

into account in the analyses in or<strong>de</strong>r to avoid additional uncontrolled variability because of<br />

age or cultivar differences.<br />

Statistical Methods<br />

1. Temporal Analysis. We <strong>de</strong>picted both annual disease inci<strong>de</strong>nce and cumulative<br />

disease inci<strong>de</strong>nce. Inci<strong>de</strong>nce is <strong>de</strong>fined as the ratio of the number of new symptomatic trees to<br />

the number of susceptible trees (living trees that never showed symptoms).<br />

2. Spatio-temporal Analysis. The data set was cut into 4 distinct periods (1983-85; 1986-<br />

89; 1990-95; 1996-99) based on the temporal evolution of disease inci<strong>de</strong>nce. We first tested<br />

the evenness of disease introduction between the 4 orchards during the years 1983-85 and<br />

1986-89, so we calculated the likelihood to see no symptomatic tree insi<strong>de</strong> 2 plots out of 4,<br />

un<strong>de</strong>r the assumption of a random introduction of the disease.<br />

In a second test, we inspected the spatial randomness of diseased trees for each period and<br />

also for the whole duration of the epi<strong>de</strong>mic. We used a method based on distances between all<br />

possible pairs of points and related to 2DCLASS (Gray et al., 1986; Nelson et al., 1992). For<br />

each possible pair of symptomatic trees, the distance between the two points was computed<br />

and assigned to a distance class (noted d). Then we performed 1000 simulations un<strong>de</strong>r the<br />

spatial randomness hypothesis by reallocating (randomly) an equal number of diseased trees<br />

within each orchard (thus conserving the structure of the group of orchards). For each<br />

simulation (noted s), the number of pairs of symptomatic trees in the distance class d, noted<br />

Nsim(s,d), was counted. Then for each of the 21 distance classes, we calculated R(d) which is<br />

the ratio between the number of observed pairs Nobs(d), and the mean number of simulated<br />

pairs Nsim (d) . Each R(d), mathematically <strong>de</strong>fined below, was then plotted with its 95%<br />

confi<strong>de</strong>nce interval.<br />

1000<br />

N<br />

∑<br />

s=<br />

sim(s,<br />

d)<br />

Nobs(d)<br />

1<br />

R(d) = , with Nsim (d) =<br />

Nsim(d)<br />

1000<br />

For the first test, the likelihood was straightforward to obtain, whereas for distance class<br />

tests the statistic R(d) was compared to an empirical 95% confi<strong>de</strong>nce interval (Diggle,1983)<br />

estimated after 1000 simulations of the null hypothesis (the 25 th and 975 th smallest values of<br />

the simulated statistic were used). The points lying outsi<strong>de</strong> the confi<strong>de</strong>nce interval indicate<br />

distance classes that <strong>de</strong>part from the null hypothesis.<br />

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