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Four species of Neotropical ticks, Amblyomma mixtum, Amblyomma cajennense, Amblyomma tonelliaeAmblyomma mixtum, Amblyomma cajennense, Amblyomma tonelliae and Amblyomma sculptum (formerly included in the catch-all name A. cajennense), have an allopatric distribution in much of their range, with areas of parapatry for at least two of them. We inferred the abiotic niches of these organisms using coefficients of a harmonic regression of the temperature and the Normalized Difference Vegetation Index (NDVI, reflecting plant stress) from remotely sensed data from MODIS satellites with 0.05 spatial resolution. Combinations of coefficients describing the phenology of these two variables pointed to divergent niche preferences, compatible with previous events of vicariance among the species. Amblyomma cajennense has been recorded in areas with small variations in temperature and NDVI. The remaining species were recorded in areas with large variations. The maximum environmental niche overlap was 73.6% between A. mixtum and A. cajennense and 73.5% betweenAmblyomma sculptum (formerly included in the catch-all name A. cajennense), have an allopatric distribution in much of their range, with areas of parapatry for at least two of them. We inferred the abiotic niches of these organisms using coefficients of a harmonic regression of the temperature and the Normalized Difference Vegetation Index (NDVI, reflecting plant stress) from remotely sensed data from MODIS satellites with 0.05 spatial resolution. Combinations of coefficients describing the phenology of these two variables pointed to divergent niche preferences, compatible with previous events of vicariance among the species. Amblyomma cajennense has been recorded in areas with small variations in temperature and NDVI. The remaining species were recorded in areas with large variations. The maximum environmental niche overlap was 73.6% between A. mixtum and A. cajennense and 73.5% between spatial resolution. Combinations of coefficients describing the phenology of these two variables pointed to divergent niche preferences, compatible with previous events of vicariance among the species. Amblyomma cajennense has been recorded in areas with small variations in temperature and NDVI. The remaining species were recorded in areas with large variations. The maximum environmental niche overlap was 73.6% between A. mixtum and A. cajennense and 73.5% betweenAmblyomma cajennense has been recorded in areas with small variations in temperature and NDVI. The remaining species were recorded in areas with large variations. The maximum environmental niche overlap was 73.6% between A. mixtum and A. cajennense and 73.5% betweenA. mixtum and A. cajennense and 73.5% between A. tonelliae and A. sculptum. Projecting these inferences on the geographical space revealed probable areas of sympatry or parapatry between A. mixtum and A. cajennense or between A. tonelliae and A. sculptum, the latter of which was confirmed with field collections. The A. sculptum distribution overlaps with that ofand A. sculptum. Projecting these inferences on the geographical space revealed probable areas of sympatry or parapatry between A. mixtum and A. cajennense or between A. tonelliae and A. sculptum, the latter of which was confirmed with field collections. The A. sculptum distribution overlaps with that ofA. mixtum and A. cajennense or between A. tonelliae and A. sculptum, the latter of which was confirmed with field collections. The A. sculptum distribution overlaps with that ofA. sculptum distribution overlaps with that of A. tonelliae in northern Argentina and Paraguay; parapatry occurs at one extreme of the conditions occupied by both species. Compared with areas of allopatry, sites with both species had consistently lower temperatures, except for 10?12 weeks during the summer, and higher NDVI values throughout the year. We hypothesise that the overlap between A. tonelliae and A. sculptum resulted from secondary contact between populations, with A. sculptum adapting to sites with high water availability to balance high summer temperatures. Additional surveys of the areas of spatial overlap among these species are necessary to elucidate the forces driving their evolution and their adaptation to the environment.in northern Argentina and Paraguay; parapatry occurs at one extreme of the conditions occupied by both species. Compared with areas of allopatry, sites with both species had consistently lower temperatures, except for 10?12 weeks during the summer, and higher NDVI values throughout the year. We hypothesise that the overlap between A. tonelliae and A. sculptum resulted from secondary contact between populations, with A. sculptum adapting to sites with high water availability to balance high summer temperatures. Additional surveys of the areas of spatial overlap among these species are necessary to elucidate the forces driving their evolution and their adaptation to the environment.A. tonelliae and A. sculptum resulted from secondary contact between populations, with A. sculptum adapting to sites with high water availability to balance high summer temperatures. Additional surveys of the areas of spatial overlap among these species are necessary to elucidate the forces driving their evolution and their adaptation to the environment.A. sculptum adapting to sites with high water availability to balance high summer temperatures. Additional surveys of the areas of spatial overlap among these species are necessary to elucidate the forces driving their evolution and their adaptation to the environment.

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