切叶蚁-菌根真菌:从一个意想不到的互惠关系观察和研究问题。

IF 2.1 Q3 MYCOLOGY Frontiers in fungal biology Pub Date : 2023-11-16 eCollection Date: 2023-01-01 DOI:10.3389/ffunb.2023.1241916
Michael F Allen, Hannah Shulman, Philip W Rundel, Thomas C Harmon, Emma L Aronson
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引用次数: 0

摘要

切叶蚁(LCAs)分布广泛,并改变了地上和地下的物理和生物结构。在新热带雨林中,它们在地上和地下制造干扰间隙,促进氧气和二氧化碳的交换。在高度多样化的新热带雨林中,丛枝菌根(AM)真菌几乎占据了森林的所有地面。几乎每立方厘米的土壤中都含有一个小球菌属真菌的菌丝网络,这种真菌形成丛枝菌根。我们的主要问题是:替代菌根——尤其是外生菌根——对某些植物物种的生存至关重要,是如何形成的?具体来说,是否存在一种抗菌根真菌的相互作用,促进了它们在这些高度多样化的生态系统中的建立?在哥斯达黎加的一个低地雨林中,LCA Atta cephalotes的巢穴覆盖了大约1.2%的陆地表面,广泛地散布在整个森林中。在土壤生物DNA测序中,我们发现许多AM真菌在它们的巢中接种,但巢中也含有外生菌根真菌、兰花菌根真菌和ericoid菌根真菌的接种,包括sinnamariense硬皮病,这是一种特殊的外生菌根植物Gnetum leyboldii的关键真菌。当巢被遗弃时,新的根生长到巢中为新的菌根协会的发展提供了机会。因此,lca形成的斑块似乎是迁移菌根植物-真菌关联建立和存活的关键场所,反过来又促进了这些群落的高度多样性。更好地了解生物之间的相互作用,包括跨界和抗菌根真菌的相互作用,将提高我们对这些生态系统如何耐受环境变化的理解。
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Leaf-cutter ants - mycorrhizal fungi: observations and research questions from an unexpected mutualism.

Leaf-cutter ants (LCAs) are widely distributed and alter the physical and biotic architecture above and below ground. In neotropical rainforests, they create aboveground and belowground disturbance gaps that facilitate oxygen and carbon dioxide exchange. Within the hyperdiverse neotropical rainforests, arbuscular mycorrhizal (AM) fungi occupy nearly all of the forest floor. Nearly every cubic centimeter of soil contains a network of hyphae of Glomeromycotina, fungi that form arbuscular mycorrhizae. Our broad question is as follows: how can alternative mycorrhizae, which are-especially ectomycorrhizae-essential for the survival of some plant species, become established? Specifically, is there an ant-mycorrhizal fungus interaction that facilitates their establishment in these hyperdiverse ecosystems? In one lowland Costa Rican rainforest, nests of the LCA Atta cephalotes cover approximately 1.2% of the land surface that is broadly scattered throughout the forest. On sequencing the DNA from soil organisms, we found the inocula of many AM fungi in their nests, but the nests also contained the inocula of ectomycorrhizal, orchid mycorrhizal, and ericoid mycorrhizal fungi, including Scleroderma sinnamariense, a fungus critical to Gnetum leyboldii, an obligate ectomycorrhizal plant. When the nests were abandoned, new root growth into the nest offered opportunities for new mycorrhizal associations to develop. Thus, the patches created by LCAs appear to be crucial sites for the establishment and survival of shifting mycorrhizal plant-fungal associations, in turn facilitating the high diversity of these communities. A better understanding of the interactions of organisms, including cross-kingdom and ant-mycorrhizal fungal interactions, would improve our understanding of how these ecosystems might tolerate environmental change.

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