<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sazatornil, F.D.</style></author><author><style face="normal" font="default" size="100%">Moré, M.</style></author><author><style face="normal" font="default" size="100%">Benitez-Vieyra, S.</style></author><author><style face="normal" font="default" size="100%">Cocucci, A.A.</style></author><author><style face="normal" font="default" size="100%">Kitching, I.J.</style></author><author><style face="normal" font="default" size="100%">Schlumpberger, B.O.</style></author><author><style face="normal" font="default" size="100%">Oliveira, P.E.</style></author><author><style face="normal" font="default" size="100%">Sazima, M.</style></author><author><style face="normal" font="default" size="100%">Amorim, F.W.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Beyond neutral and forbidden links: morphological matches and the assembly of mutualistic hawkmoth-plant networks</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Animal Ecology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ARGENTINA</style></keyword><keyword><style  face="normal" font="default" size="100%">BRAZIL</style></keyword><keyword><style  face="normal" font="default" size="100%">COEVOLUTION</style></keyword><keyword><style  face="normal" font="default" size="100%">COMMUNITY STRUCTURE</style></keyword><keyword><style  face="normal" font="default" size="100%">ECOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">FORAGING</style></keyword><keyword><style  face="normal" font="default" size="100%">MORPHOLOGICAL FORBIDDEN LINKS HYPOTHESIS</style></keyword><keyword><style  face="normal" font="default" size="100%">MORPHOLOGICAL MATCH HYPOTHESIS</style></keyword><keyword><style  face="normal" font="default" size="100%">NEUTRAL HYPOTHESIS</style></keyword><keyword><style  face="normal" font="default" size="100%">PLANT-POLLINATOR NETWORKS</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATION</style></keyword><keyword><style  face="normal" font="default" size="100%">PROBOSCIS</style></keyword><keyword><style  face="normal" font="default" size="100%">RAREFACTION</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword><keyword><style  face="normal" font="default" size="100%">WORLDMAP1</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">10/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">85</style></volume><pages><style face="normal" font="default" size="100%">1586-1594</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;quot;1. A major challenge in evolutionary ecology is to understand how co-evolutionary processes&lt;br /&gt;
	shape patterns of interactions between species at community level. Pollination of flowers with&lt;br /&gt;
	long corolla tubes by long-tongued hawkmoths has been invoked as a showcase model of&lt;br /&gt;
	co-evolution. Recently, optimal foraging models have predicted that there might be a close&lt;br /&gt;
	association between mouthparts&amp;rsquo; length and the corolla depth of the visited flowers, thus&lt;br /&gt;
	favouring trait convergence and specialization at community level.&lt;br /&gt;
	2. Here, we assessed whether hawkmoths more frequently pollinate plants with floral tube&lt;br /&gt;
	lengths similar to their proboscis lengths (morphological match hypothesis) against abundance-&lt;br /&gt;
	based processes (neutral hypothesis) and ecological trait mismatches constraints (forbidden&lt;br /&gt;
	links hypothesis), and how these processes structure hawkmoth&amp;ndash;plant mutualistic&lt;br /&gt;
	networks from five communities in four biogeographical regions of South America.&lt;br /&gt;
	3. We found convergence in morphological traits across the five communities and that the&lt;br /&gt;
	distribution of morphological differences between hawkmoths and plants is consistent with&lt;br /&gt;
	expectations under the morphological match hypothesis in three of the five communities. In&lt;br /&gt;
	the two remaining communities, which are ecotones between two distinct biogeographical&lt;br /&gt;
	areas, interactions are better predicted by the neutral hypothesis.&lt;br /&gt;
	4. Our findings are consistent with the idea that diffuse co-evolution drives the evolution of&lt;br /&gt;
	extremely long proboscises and flower tubes, and highlight the importance of morphological&lt;br /&gt;
	traits, beyond the forbidden links hypothesis, in structuring interactions between mutualistic&lt;br /&gt;
	partners, revealing that the role of niche-based processes can be much more complex than&lt;br /&gt;
	previously known.&amp;quot;&lt;/p&gt;
</style></abstract><section><style face="normal" font="default" size="100%">1586</style></section></record></records></xml>