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Host plant shifts and transitions into new adaptive zones in leafhoppers: the example of Macropsinae (Homoptera: Auchenorrhyncha: Cicadellidae) of Russia and adjacent countries

机译:寄主植物转移并过渡到叶蝉的新适应区中:俄罗斯和邻近国家的Macropsinae(Homooptera:Auchenorrhyncha:Cicadellidae)

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The modes of diversification of Palaearctic Macropsinae (Homoptera: Auchenorrhyncha: Cicadellidae) are reconstructed based on data on their host plants and distribution in Russia and the adjacent territories. Macropsinae (Homoptera: Auchenorrhyncha: Cicadellidae) is originally an Oriental group, which penetrated into the Palaearctic from Southeast Asia. The genus Pediopsoides and species of the genus Macropsis that feed on East Asian oaks have not dispersed beyond broadleaf forests of the Eastern Palaearctic. Apparently, Pediopsis and elm-feeding species of Macropsis initially dispersed throughout the entire broadleaf forest zone. Division of this zone into two widely separated parts in temperate areas of Europe and East Asia (nemoral disjunction), produced closely related vicariant pairs of sister species. The genus Oncopsis and species of Macropsis feeding on Salicaceae dispersed throughout the entire Palaearctic following their host plants. Both lineages penetrated into riparian forests of the foothills and midlands of Central Asia, where they produced endemic species. The Central Asian Macropsis lineage shifted from Salicaceae to trees and shrubs of unrelated families (wild roses, barberry, oleaster, and sea-buckthorn) growing in the same biotopes. Subsequent diversification on those plants produced several separate host-associated species-groups, some of which penetrated following their hosts from riparian forests into arid habitats. One such lineage apparently shifted from shrubs to wormwood species (Artemisia spp.) and thus gave rise to the genus Macropsidius. This genus underwent adaptive radiation on wormwood species in the plains of South Kazakhstan and Central Asia; advancing westward, it formed secondary centres of diversity in Transcaucasia and the Mediterranean. Finally, some lineage of Macropsidius (or its sister-group) switched from feeding on Artemisia to polyphagy, yielding the ancestral form of the genus Hephathus. In general, the evolution of the Macropsis-Macropsidius-Hephathus lineage in the Palaearctic closely followed the classical Simpsonian model: the group underwent diversification within a particular adaptive zone, then one lineage entered a new adaptive zone and secondarily diversified there, etc. Transitions into new adaptive zones by different Macropsinae lineages were probably caused by one of two factors: shift to a new plant unrelated to the original host (e.g., from Salicaceae to plants of other families) or adaptation to new microclimatic conditions (penetration from riparian forests into open arid habitats).
机译:根据有关古宿主Macroppesinae(Homooptera:Auchenorrhyncha:Cicadellidae)的寄主植物及其在俄罗斯及邻近地区的分布数据,重建了其多样性模式。巨猿科(Macroppsinae,原名:Auchenorrhyncha:Cicadellidae)最初是一个东方群,从东南亚渗透到古太平洋。以东亚橡树为食的Pediopsoides属和Macropsis属的物种尚未分散到东古北洋的阔叶林之外。显然,Macroppsis的小脚虫和榆食性物种最初散布在整个阔叶林地带。在欧洲和东亚的温带地区,该区域被划分为两个彼此分离的部分(神经分离),产生了紧密相关的双亲姊妹物种。以杨柳科为食的大头菜属和巨足类属在其寄主植物后散布在整个古古生物学中。两种血统都渗透到中亚山麓和中部的河岸森林中,在那里它们产生了特有物种。中亚地区的Macropsis谱系从杨柳科转移到了在相同的生物群落中生长的无关家庭(野生玫瑰,伏牛花,苦竹和沙棘)的树木和灌木。随后这些植物的多样化产生了几个独立的寄主相关物种组,其中一些随着它们的寄主从河岸森林渗透到干旱的栖息地。一种这样的谱系显然从灌木变成了艾草种(蒿属),因此产生了Macroppsidius属。该属对哈萨克斯坦南部和中亚平原的艾草物种进行了适应性辐射;向西推进,它形成了Transcaucasia和地中海的次生多样性中心。最终,巨猿属(或它的姐妹群)的某些谱系从以蒿为食转变为多食,从而产生了赫菲斯属的祖先形式。总的来说,古生物学中的Macroppsis-Macropsidius-Hephathus谱系的进化紧密遵循经典的Simpsonian模型:该群体在特定的适应区内进行了多样化,然后一个谱系进入了一个新的适应区,然后在此进行了多样化,依此类推。不同的Macropsinae世系的新适应区可能是由以下两个因素之一引起的:转移到与原始寄主无关的新植物(例如,从杨柳科转移到其他科的植物)或适应新的微气候条件(从河岸森林渗透到开放干旱的栖息地)。

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