DO IMAGE-FORMING EYES PROMOTE EVOLUTIONARY DIVERSIFICATION?

It has been suggested that image-forming eyes promote the evolutionary diversification (measured by species richness) of the groups that possess them. Several different processes could give rise to this effect, including diversifying selection in a new adaptive zone (or zones) and a reduced rate of extinction due to enhanced competitive abilities. I tested the generality of the hypothesis that imaging eyes increase net speciation by comparing extant species numbers of 12 groups that have such eyes (as categorized by Land and Fernald 1992) with those of their cladistic sister groups that lack such organs. Even assuming the published hypotheses of phylogenetic relationships that most favor increased net speciation of visual groups, these comparisons show no significant association between imaging eyes and species richness. Increased activity, as indicated by published accounts of locomotory speed, is significantly associated with the evolution of image-forming eyes. This suggests that a large “visual adaptive zone” might be characterized by relatively high activity. However, when diversity comparisons are limited to eight cases in which the evolution of imaging eyes is associated with increased activity, there is still no significant association between such eyes and species richness. The fossil record indicates that the only visual groups that have undergone major evolutionary radiations evolved imaging eyes early in the history of metazoans (before the Silurian). The radiations of these early groups may have largely filled up niches for visual animals and thus prevented the subsequent proliferation of other groups with image-forming eyes. Alternatively, it may be that image-forming eyes have no exceptional effect on diversification or that their effects are obscured by other factors in the long run.     

A preliminary classification of evolutionary radiations

Rapid increases in taxonomic diversity are generally described as adaptive or evolutionary radiations. Such radiations differ widely in the rate and extent of morphologic innovation, taxonomic diversification and phylogenetic breadth, suggesting that several patterns, and likely processes, are involved. At least four distinct patterns of evolutionary radiation can be identified: novelty events, which generate new morphological complexity (altering the body plan of the group under consideration) but not necessarily with the associated production of many lower taxa; broad diversification events involving many independent lineages that undergo diversification, generate many new species and are driven by new ecological opportunities; economic radiations of a limited group of ecologically (but not necessarily phylogenetically) related clades exploiting a limited new ecologic opportunity; and adaptive radiations that may occur at any taxonomic level, but involve a rapid increase in diversity within a single clade, including “true”; adaptive radiations. Many events produce simple diversity increases with no corresponding increase in genetic/developmental/morphological/behavioral sophistication, but the most evolutionarily interesting events add new levels of complexity.     

Are three‐dimensional spider webs defensive adaptations?

Spider webs result from complex behaviours that have evolved under many selective pressures. Webs have been primarily considered to be foraging adaptations, neglecting the potential role of predation risk in the evolution of web architecture. The ecological success of spiders has been attributed to key innovations in how spiders use silk to capture prey, especially the invention of chemically adhesive aerial two‐dimensional orb webs. However, araneoid sheet web weavers transformed the orb architecture into three‐dimensional webs and are the dominant group of aerial web‐building spiders world‐wide, both in numbers and described species diversity. We argue that mud‐dauber wasps are major predators of orbicularian spiders, and exert a directional selective pressure to construct three‐dimensional webs such that three‐dimensional webs are partly defensive innovations. Furthermore, patterns of diversification suggest that escape from wasp predators may have facilitated diversification of three‐dimensional web‐building spiders.     

Adaptive radiation and coevolution — pollination biology case studies

The impact of coevolutionary interaction between species on adaptive radiation processes is analysed with reference to pollination biology case studies. Occasional colonization of archipelagos can bring together coevolving partners and cause coradiation of the colonizing species, e.g. the drepanidids and the lobelioids on Hawaii. Permanent reciprocal selective pressure between pairs of coevolving species can lead to a coevolutionary race and rapid evolutionary change. This is exemplified by spurred flowers and long-tongued flower-visitors. The geographic patterning of diffuse coevolution systems can lead to dramatic changes in species interactions. In different populations, interaction between pollinating and seed-parasitizing Greya moths and their host plants varies from mutualism to commensalism and antagonism, depending on the presence of copollinators. Asymmetrical coevolution between angiosperms and oligolectic flower-visitors may facilitate rapid reproductive isolation of populations following a food-plant switch, if the oligoleges use their specific food plants as the rendezvous sites. Diffuse coevolution between angiosperm species and pollinating insects may cause frequent convergent evolution of floral traits such as nectar reward instead of pollen reward, floral guides, zygomorphic flowers, or mimicry of pollen signals, since the multiple plant species experience similar selective pressures via the coevolving partners. Patterns of angiosperm adaptive radiation are highlighted in the context of coevolution with pollinators.     

裸子植物psbA基因分子进化式样的研究

为阐明裸子植物对陆生生境生态响应的分子机制,以新近的裸子植物分类系统为指导,基于psb A基因编码全序列对4亚纲53种代表植物进行分子进化分析。首先,依据\"放松分子钟\"模型重建裸子植物在时间尺度下系统发育关系;其次,采用6个模型(MEC/JTT、MEC/cp REV、M5、M7、M8、M8a)估测氨基酸位点ω值,并对各模型结果进行统计检测;随后,利用Bootstrap方法检PSBA蛋白内部氨基酸位点的共进化动态。结果表明,系统树提示的物种分化历程支持前期分类结果;光合系统反应中心核心PSBA蛋白有3个氨基酸位点(13、19和243)曾经受正选择压力;PSBA蛋白内部有多对氨基酸位点间构成了共进化网络。因此,psb A基因编码序列具有作为描绘裸子植物系统发育关系标记的潜力,PSBA蛋白部分位点经历了适应性进化,通过位点间共进化网络协同作用方式辅助裸子植物响应陆生生境。