Volume 20, Issue 3, Pages (February 2010)

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From: Metacontrast masking within and between visual channels: Effects of orientation and spatial frequency contrasts Journal of Vision. 2010;10(6):12.
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Volume 20, Issue 3, Pages 215-222 (February 2010) Fishery Discards Impact on Seabird Movement Patterns at Regional Scales  Frederic Bartumeus, Luca Giuggioli, Maite Louzao, Vincent Bretagnolle, Daniel Oro, Simon A. Levin  Current Biology  Volume 20, Issue 3, Pages 215-222 (February 2010) DOI: 10.1016/j.cub.2009.11.073 Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 1 Shearwater Foraging Trajectories in the Western Mediterranean Region Examples of single trajectories for the Cory's shearwater (upper panels) and the Balearic shearwater (lower panels). For illustrative purposes, we have assigned each of the trajectories to one of the two possible scenarios under study: absence (left panels) or presence (right panels) of fishery activity. For a given trajectory, if less than 50% of the total number of locations occurred in the presence of fishery activities, we considered that trajectory as a “no fisheries” trajectory; otherwise, the trajectory was considered as a “fisheries” trajectory. For the four trajectories shown, the percentage of locations occurring in the presence of fishery activities are 16% (upper left), 68% (upper right), 37% (lower left), and 65% (lower right). The percentage differences among trajectories are not great, but they are large enough to recover the average behavior of the spatial kernels measured in the presence and in the absence of fisheries when pooling the flying segments at the population level. Pelagic and nonpelagic flights are characterized by dashed lines and bold solid lines, respectively. The limit of the foraging grounds is at the isobath of 1000 m, represented here by a continuous line. Breeding colonies are indicated by stars. It can be observed that large, nonpelagic displacements are more prone to occur in the two trajectories associated with periods with no fishery activity (left panels) than in the two periods with more fishery activity (right panels). For more details on the data set, see Figure S1 and Table S1. Current Biology 2010 20, 215-222DOI: (10.1016/j.cub.2009.11.073) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 2 Sequential Pointwise Model Comparison We contrast the exponential (black), truncated power-law (red), gamma (green), lognormal (dark blue), and stretched exponential (light blue) distributions for both the spatial kernel (i.e., F(r), A and B) and the site fidelity kernel (i.e., SA(t), A = 50 km × 50 km, C and D) observed in the absence (A and C) and in the presence (B and D) of fisheries. A value of corrected and weighted Akaike information criteria (wAICc) = 1 gives the maximum weight of evidence in favor of one of the models that are compared. Upper x axis shows the number of data points used in each comparison; lower x axis shows the approximate value of each data point labeled in the upper x axis. Different xmin values were successively chosen from the minimum to the maximum value (without the last five values) of the observed traveling distances (A and B), and site fidelity times (C and D). For further sequential pointwise statistical analyses, see Figures S2 and S3. Current Biology 2010 20, 215-222DOI: (10.1016/j.cub.2009.11.073) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 3 Sequential Pointwise Goodness of Fits Goodness of fits are based on Monte Carlo replicates and the computation of Kolmogorov-Smirnov tests as in Clauset et al. [30]. Statistical validation was performed for exponential (black), truncated power-law (red), gamma (green), lognormal (dark blue), and stretched exponential (light blue) distributions for both the spatial kernel (i.e., F(r), A and B) and the site fidelity kernel (i.e., SA(t), A = 50 km × 50 km, C and D) observed in the absence (A and C) and in the presence (B and D) of fisheries. For each data point, if the p value is much less than 1 (i.e., p < 0.1), it is unlikely that the subset of data including all of the values above that point is drawn from the corresponding model; therefore, the tail model can be ruled out. For further sequential pointwise statistical analyses, see Figures S2 and S3. Current Biology 2010 20, 215-222DOI: (10.1016/j.cub.2009.11.073) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 4 Cumulative and Probability Density Distribution Plots Cumulative probability distribution plots for the spatial kernel (i.e., F(r), A and B) and the site fidelity kernel (i.e., SA(t), A = 50 km × 50 km, C and D) in the absence (A and C) and in the presence (B and D) of fishery activities. Insets show log-binned, normalized plots of the behavior of the probability density functions. Red and dashed lines illustrate the behavior of the best fits (see Table 1) for the tail of the distribution in both the cumulative and the probability density forms. The exponent of the site fidelity kernel density function is δ = 1 − β because SA(t)∼t−β. See also Figure S4. Current Biology 2010 20, 215-222DOI: (10.1016/j.cub.2009.11.073) Copyright © 2010 Elsevier Ltd Terms and Conditions