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在不同降水量条件下,天敌和竞争的系统性减少近似于水牛草在其原生范围内的入侵性。

Systematic reduction of natural enemies and competition across variable precipitation approximates buffelgrass invasiveness () in its native range.

作者信息

Rhodes Aaron C, Plowes Robert M, Bowman Elizabeth A, Gaitho Aimee, Ng'Iru Ivy, Martins Dino J, Gilbert Lawrence E

机构信息

Brackenridge Field Laboratory The University of Texas at Austin Austin Texas USA.

Hiro Technologies, Inc Austin Texas USA.

出版信息

Ecol Evol. 2024 May 11;14(5):e11350. doi: 10.1002/ece3.11350. eCollection 2024 May.

DOI:10.1002/ece3.11350
PMID:38737568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11087885/
Abstract

Invasive grasses cause devastating losses to biodiversity and ecosystem function directly and indirectly by altering ecosystem processes. Escape from natural enemies, plant-plant competition, and variable resource availability provide frameworks for understanding invasion. However, we lack a clear understanding of how natural stressors interact in their native range to regulate invasiveness. In this study, we reduced diverse guilds of natural enemies and plant competitors of the highly invasive buffelgrass across a precipitation gradient throughout major climatic shifts in Laikipia, Kenya. To do this, we used a long-term ungulate exclosure experiment design across a precipitation gradient with nested treatments that (1) reduced plant competition through clipping, (2) reduced insects through systemic insecticide, and (3) reduced fungal associates through fungicide application. Additionally, we measured the interaction of ungulates on two stem-boring insect species feeding on buffelgrass. Finally, we measured a multiyear smut fungus outbreak. Our findings suggest that buffelgrass exhibits invasive qualities when released from a diverse group of natural stressors in its native range. We show natural enemies interact with precipitation to alter buffelgrass productivity patterns. In addition, interspecific plant competition decreased the basal area of buffelgrass, suggesting that biotic resistance mediates buffelgrass dominance in the home range. Surprisingly, systemic insecticides and fungicides did not impact buffelgrass production or reproduction, perhaps because other guilds filled the niche space in these highly diverse systems. For example, in the absence of ungulates, we showed an increase in host-specific stem-galling insects, where these insects compensated for reduced ungulate use. Finally, we documented a smut outbreak in 2020 and 2021, corresponding to highly variable precipitation patterns caused by a shifting Indian Ocean Dipole. In conclusion, we observed how reducing natural enemies and competitors and certain interactions increased properties related to buffelgrass invasiveness.

摘要

入侵性草本植物通过改变生态系统过程,直接或间接地给生物多样性和生态系统功能造成毁灭性损失。摆脱天敌、植物间竞争以及可变的资源可利用性,为理解入侵现象提供了框架。然而,我们对于自然压力源在其原生范围内如何相互作用以调节入侵性缺乏清晰的认识。在本研究中,我们在肯尼亚莱基皮亚经历主要气候变化的整个降水梯度范围内,减少了极具入侵性的水牛草的多种天敌和植物竞争者。为此,我们采用了一项长期有蹄类动物围栏实验设计,该设计具有降水梯度以及嵌套处理,包括:(1)通过修剪减少植物竞争;(2)通过内吸性杀虫剂减少昆虫;(3)通过施用杀真菌剂减少真菌共生体。此外,我们测量了有蹄类动物对以水牛草为食的两种蛀茎昆虫物种的影响。最后我们测量了一场持续多年的黑粉菌爆发情况。我们的研究结果表明,当水牛草在其原生范围内摆脱了多种自然压力源时,它就展现出入侵特性。我们发现天敌与降水相互作用,改变了水牛草的生产力模式。此外,种间植物竞争减小了水牛草的基部面积,这表明生物抗性在原生范围内调节着水牛草的优势地位。令人惊讶的是,内吸性杀虫剂和杀真菌剂并未影响水牛草的生长或繁殖,这可能是因为在这些高度多样化的系统中,其他类群填补了生态位空间。例如,在没有有蹄类动物的情况下,我们发现寄主专化的蛀茎昆虫数量增加,这些昆虫弥补了有蹄类动物啃食减少的影响。最后,我们记录到在2020年和2021年发生了黑粉菌爆发,这与印度洋偶极移动导致的高度多变的降水模式相对应。总之,我们观察到减少天敌和竞争者以及某些相互作用如何增加了与水牛草入侵性相关的特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/117b42bc513e/ECE3-14-e11350-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/8ff57cc71c7c/ECE3-14-e11350-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/5c2c49aaa673/ECE3-14-e11350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/15ab0540d037/ECE3-14-e11350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/9ab6d7c27fd2/ECE3-14-e11350-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/8fcfb8fa1496/ECE3-14-e11350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/4c7ed2709f22/ECE3-14-e11350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/57a706aaa377/ECE3-14-e11350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/b9131a537bda/ECE3-14-e11350-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/117b42bc513e/ECE3-14-e11350-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/8ff57cc71c7c/ECE3-14-e11350-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/5c2c49aaa673/ECE3-14-e11350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/15ab0540d037/ECE3-14-e11350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/9ab6d7c27fd2/ECE3-14-e11350-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/8fcfb8fa1496/ECE3-14-e11350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/4c7ed2709f22/ECE3-14-e11350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/57a706aaa377/ECE3-14-e11350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/b9131a537bda/ECE3-14-e11350-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e19/11087885/117b42bc513e/ECE3-14-e11350-g010.jpg

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