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Ecole Nationale Supérieure Agronomique de Montpellier ... - CIAM

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shows that the proportion of missing plants has a minor impact on the power of the test (at<br />

least up to 10%), whereas a <strong>de</strong>creasing lattice size reduces the power of the test, which<br />

nevertheless remains high in a 12 × 30 lattice (approximately 90%). Concerning the<br />

robustness of the test to violations of its two basic assumptions, the method is not robust to<br />

the simulated bor<strong>de</strong>r effect because the type I error grows from 5% to > 15%. Conversely, the<br />

<strong>de</strong>pen<strong>de</strong>nce between t1 cases and missing plants (2% located at random) has no major effect<br />

(Table 4).<br />

ESFY data set. The preliminary analysis using 2DCORR indicated that neither t1 cases<br />

nor t2 cases significantly differed from a random pattern, even without applying the<br />

conservative Bonferroni correction. The cumulative probability function almost perfectly<br />

matched what would be expected if diseased plants were located at random (not shown).<br />

Consequently, in or<strong>de</strong>r to analyze the <strong>de</strong>pen<strong>de</strong>nce between early and late infections, we<br />

performed Test 1. This bilateral test, with a global 5% significance level and 1,000<br />

simulations of H0, indicated a trend toward intra-row aggregation between t1 cases and t2<br />

cases: P = 0.084 within a distance of two trees (Fig. 3A).<br />

PPV data set. The preliminary analysis indicated that both t1 cases and t2 cases were<br />

significantly clustered (with a P-value below the Bonferroni threshold) for the first distance<br />

class along rows for t1 cases, and for the first distance class along and across rows for t2 cases.<br />

This was confirmed by a formal Kolmogorov-Smirnov test for t2 cases (significant at<br />

P < 0.05). Hence, to analyze the <strong>de</strong>pen<strong>de</strong>nce between early and late infections, we used Test<br />

3. This bilateral test with a global 5% significance level and 663 simulations of H0 indicated<br />

that t1 cases and t2 cases were tightly aggregated, with P-values ranging from P = 0.012 to<br />

P = 0.045 up to a distance of 10 m (Fig. 3B).<br />

DISCUSSION<br />

The analysis of epi<strong>de</strong>mics simultaneously in space and time can provi<strong>de</strong> crucial<br />

indications about the process of disease spread. Up to now, however, we were lacking a<br />

nonparametric method to handle disease clustering at each date and disease censoring by t1<br />

diseased plants and by missing plants. This has hampered the initial exploration of<br />

spatiotemporal data when plants are regularly spaced and mapped individually. In this article,<br />

we have presented a framework to test the hypothesis that the location of newly diseased<br />

plants is in<strong>de</strong>pen<strong>de</strong>nt of the location of previously diseased plants. In this permutation method<br />

<strong>de</strong>dicated to the exploration of spatiotemporal data, the significant spatial structures at each<br />

date and the censoring are taken into account. This method can provi<strong>de</strong> indications on the role<br />

of short-distance plant-to-plant transmission, which is fundamental for both epi<strong>de</strong>miological<br />

studies and disease management.<br />

The validation of our method on numerous simulated bivariate point patterns shows that it<br />

is powerful in the <strong>de</strong>tection of <strong>de</strong>pen<strong>de</strong>nt patterns (even for a relatively small lattice size such<br />

as 12 × 30). It also shows that, when in<strong>de</strong>pen<strong>de</strong>nt patterns are simulated, the rate of rejection<br />

of the hypothesis of in<strong>de</strong>pen<strong>de</strong>nce is around the pre<strong>de</strong>fined 5% significance level, or slightly<br />

below for small lattices. Of course, the accuracy and power of the method could be assessed<br />

for other combinations of the parameters that <strong>de</strong>fine the processes; the properties of the test in<br />

any specific situation can be studied numerically as exemplified in this article, by simulating<br />

the appropriate patterns.<br />

The analysis of data sets from ESFY and PPV epi<strong>de</strong>mics <strong>de</strong>monstrates the practical<br />

application of this method that allowed testing general spatiotemporal hypotheses related to<br />

the processes of disease spread for both diseases. For example, as the epi<strong>de</strong>miology of ESFY<br />

remains poorly characterized, secondary transmission at the orchard scale is still an open<br />

question. The test of in<strong>de</strong>pen<strong>de</strong>nce indicated a trend toward within-row aggregation between<br />

the trees showing symptoms early in the epi<strong>de</strong>mic and those <strong>de</strong>veloping disease later; this<br />

trend is consistent with short-range intra-orchard transmission. However, the same analyses<br />

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