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Abstract Most herbivorous insects are diet specialists in spite of the apparent advantages of being a generalist. This conundrum might be explained by fitness trade‐offs on alternative host plants, yet the evidence of such trade‐offs has been elusive. Another hypothesis is that specialization is nonadaptive, evolving through neutral population‐genetic processes and within the bounds of historical constraints. Here, we report on a striking lack of evidence for the adaptiveness of specificity in tropical canopy communities of armored scale insects. We find evidence of pervasive diet specialization, and find that host use is phylogenetically conservative, but also find that more‐specialized species occur on fewer of their potential hosts than do less‐specialized species, and are no more abundant where they do occur. Of course local communities might not reflect regional diversity patterns. But based on our samples, comprising hundreds of species of hosts and armored scale insects at two widely separated sites, more‐specialized species do not appear to outperform more generalist species.
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Evolution of specialized microbial cooperation in dynamic fluids
Abstract Here, we study the evolution of specialization using realistic computer simulations of bacteria that secrete two public goods in a dynamic fluid. Through this first‐principles approach, we find physical factors such as diffusion, flow patterns and decay rates are as influential as fitness economics in governing the evolution of community structure, to the extent that when mechanical factors are taken into account, (a) generalist communities can resist becoming specialists despite the invasion fitness of specialization; (b) generalist and specialists can both resist cheaters despite the invasion fitness of free‐riding; and (c) multiple community structures can coexist despite the opposing force of competitive exclusion. Our results emphasize the role of spatial assortment and physical forces on niche partitioning and the evolution of diverse community structures.
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- Award ID(s):
- 1805157
- PAR ID:
- 10458007
- Publisher / Repository:
- Oxford University Press
- Date Published:
- Journal Name:
- Journal of Evolutionary Biology
- Volume:
- 33
- Issue:
- 3
- ISSN:
- 1010-061X
- Format(s):
- Medium: X Size: p. 256-269
- Size(s):
- p. 256-269
- Sponsoring Org:
- National Science Foundation
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