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. 2017 May 31;125(5):057008.
doi: 10.1289/EHP57.

Expansion of the Lyme Disease Vector Ixodes Scapularis in Canada Inferred from CMIP5 Climate Projections

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Expansion of the Lyme Disease Vector Ixodes Scapularis in Canada Inferred from CMIP5 Climate Projections

Michelle McPherson et al. Environ Health Perspect. .

Abstract

Background: A number of studies have assessed possible climate change impacts on the Lyme disease vector, Ixodes scapularis. However, most have used surface air temperature from only one climate model simulation and/or one emission scenario, representing only one possible climate future.

Objectives: We quantified effects of different Representative Concentration Pathway (RCP) and climate model outputs on the projected future changes in the basic reproduction number (R0) of I. scapularis to explore uncertainties in future R0 estimates.

Methods: We used surface air temperature generated by a complete set of General Circulation Models from the Coupled Model Intercomparison Project Phase 5 (CMIP5) to hindcast historical (1971-2000), and to forecast future effects of climate change on the R0 of I. scapularis for the periods 2011-2040 and 2041-2070.

Results: Increases in the multimodel mean values estimated for both future periods, relative to 1971-2000, were statistically significant under all RCP scenarios for all of Nova Scotia, areas of New Brunswick and Quebec, Ontario south of 47°N, and Manitoba south of 52°N. When comparing RCP scenarios, only the estimated R0 mean values between RCP6.0 and RCP8.5 showed statistically significant differences for any future time period.

Conclusion: Our results highlight the potential for climate change to have an effect on future Lyme disease risk in Canada even if the Paris Agreement's goal to keep global warming below 2°C is achieved, although mitigation reducing emissions from RCP8.5 levels to those of RCP6.0 or less would be expected to slow tick invasion after the 2030s. https://doi.org/10.1289/EHP57.

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Figures

Grid map of Northings (y-axis) and Eastings (x-axis) showing the regions where at least one tick and where no tick was found according to the surveillance conducted 2003–2012. The second grid map of Northings (y-axis) and Eastings (x-axis) plots the R0 estimates for the period 1971–2000.
Figure 1.
Top: Data from active tick surveillance conducted between both 2003–2012 (Bouchard et al. 2015) and 2008–2013 (Ogden et al. 2014a). Locations where at least one I. scapularis tick has been found are marked by red triangles. White triangles mark locations where no I. scapularis ticks were collected. Bottom: Historical multimodel mean R0 estimates for the period 1971–2000. The R0 bar provides a color gradient showing the colors, which correspond to specific R0 values. The numbers around both the top and bottom maps depict the northings and eastings associated with the domain.
Six grid maps plotting Northings (y-axis) and Eastings (x-axis). (a), (b) and (c) plot the R0 values for 1971–2000, RCP45 2011–2040, and RCP45 2041–2070, respectively. (d), (e) and (f) plot the 95% confidence interval for 1971–2000, RCP45 2011–2040, and RCP45 2041–2070, respectively.
Figure 2.
Multimodel mean R0 values for I. scapularis (maps a−c) and the climate model variability (95% confidence interval) (maps d−f) for the period 1971–2000 using the historical simulation and for the periods 2011–2040 and 2041–2070 using RCP4.5 simulations. R0>1 values were mapped for areas east of the Rocky Mountains and for elevations below 500 m. The R0 bar provides a color gradient showing the colors, which correspond to specific R0 values. The numbers around the maps depict the Northings and Eastings associated with the domain. Black stippling in maps b and c shows the spatial distribution of statistically significant changes in R0 between each future time period (2011–2040 and 2041–2070) and the historical time period (1971–2000). Statistical significance was calculated using the Kolmogorov-Smirnov test.
Six grid maps plotting Northings (y-axis) and Eastings (x-axis). (a), (b) and (c) plot the R0 values for 1971–2000, RCP85 2011–2040, and RCP85 2041–2070, respectively. (d), (e) and (f) plot the 95% confidence interval for 1971–2000, RCP85 2011–2040, and RCP85 2041–2070, respectively.
Figure 3.
Multimodel mean R0 values for I. scapularis (maps a−c) and the climate model variability (95% confidence interval) (maps d−f) for the period 1971–2000 using the historical simulations and for the periods 2011–2040 and 2041–2070 using RCP8.5 simulations. R0>1 values were mapped for areas east of the Rocky Mountains and for elevations below 500 m. The R0 bar provides a color gradient showing the colors, which correspond to specific R0 values. The numbers around the maps depict the Northings and Eastings associated with the domain. Black stippling in maps b and c shows the spatial distribution of statistically significant changes in R0 between each future time period (2011–2040 and 2041–2070) and the historical time period 1971–2000. Statistical significance was calculated using the Kolmogorov-Smirnov test.
Two shaded line graphs show R0 values (y-axis) for the years 1914, 1940, 1967, 1993, 2010, 2046, 2073, and 2099 (x-axis) for Southern Ontario and Nova Scotia. The simulation lines indicate historical period, RCP26, RCP45, RCP60, and RCP80.
Figure 4.
Annual estimates of the R0 multimodel mean and the climate model variability (95% confidence interval) for Ontario south of 50°N (left) and Nova Scotia (right).
Shaded line graph shows R0 values (y-axis) for the years 1914, 1940, 1967, 1993, 2010, 2046, 2073, and 2099 (x-axis) for Northern Ontario. The simulation lines indicate historical period, RCP26, RCP45, RCP60, and RCP80.
Figure 5.
Annual estimates of the R0 multimodel mean and the model variability (95% confidence interval) for Ontario north of 50°N.

Comment in

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