Multiple components of plant diversity loss determine herbivore phylogenetic diversity in a subtropical forest experiment

Research output: Journal contributionsJournal articlesResearchpeer-review

Standard

Multiple components of plant diversity loss determine herbivore phylogenetic diversity in a subtropical forest experiment. / Wang, Ming-Qiang; Li, Yi; Chesters, Douglas et al.

In: Journal of Ecology, Vol. 107, No. 6, 01.11.2019, p. 2697-2712.

Research output: Journal contributionsJournal articlesResearchpeer-review

Harvard

Wang, M-Q, Li, Y, Chesters, D, Anttonen, P, Bruelheide, H, Chen, J-T, Durka, W, Guo, P-F, Haerdtle, W, Ma, K, Michalski, SG, Schmid, B, von Oheimb, G, Wu, C-S, Zhang, N-L, Zhou, Q-S, Schuldt, A & Zhu, C-D 2019, 'Multiple components of plant diversity loss determine herbivore phylogenetic diversity in a subtropical forest experiment', Journal of Ecology, vol. 107, no. 6, pp. 2697-2712. https://doi.org/10.1111/1365-2745.13273

APA

Wang, M-Q., Li, Y., Chesters, D., Anttonen, P., Bruelheide, H., Chen, J-T., Durka, W., Guo, P-F., Haerdtle, W., Ma, K., Michalski, S. G., Schmid, B., von Oheimb, G., Wu, C-S., Zhang, N-L., Zhou, Q-S., Schuldt, A., & Zhu, C-D. (2019). Multiple components of plant diversity loss determine herbivore phylogenetic diversity in a subtropical forest experiment. Journal of Ecology, 107(6), 2697-2712. https://doi.org/10.1111/1365-2745.13273

Vancouver

Wang M-Q, Li Y, Chesters D, Anttonen P, Bruelheide H, Chen J-T et al. Multiple components of plant diversity loss determine herbivore phylogenetic diversity in a subtropical forest experiment. Journal of Ecology. 2019 Nov 1;107(6):2697-2712. Epub 2019 Aug 20. doi: 10.1111/1365-2745.13273

Bibtex

@article{39fd6d4aec7a450d862a7402f8107c72,
title = "Multiple components of plant diversity loss determine herbivore phylogenetic diversity in a subtropical forest experiment",
abstract = " Plant diversity loss can alter higher trophic‐level communities via non‐random species interactions, which in turn may cascade to affect key ecosystem functions. These non‐random linkages might be best captured by patterns of phylogenetic diversity, which take into account co‐evolutionary dependencies. However, lack of adequate phylogenetic data of higher trophic levels hampers our mechanistic understanding of biodiversity relationships in species‐rich ecosystems. We used DNA barcoding to generate data on the phylogenetic diversity of lepidopteran caterpillars in a large‐scale forest biodiversity experiment in subtropical China. We analysed how different metrics of lepidopteran phylogenetic diversity (Faith's PD, MPD, MNTD) and taxonomic diversity were influenced by multiple components of tree diversity (taxonomic, functional, phylogenetic). Our data from six sampling periods represent 7,204 mitochondrial cytochrome c oxidase subunit I (COI) sequences of lepidopteran larvae, clustered into 461 molecular operational taxonomic units. Lepidopteran abundance, the effective number of species (irrespective of the focus on rare or common species) and Faith's PD and MPD (reflecting basal evolutionary splits), but not MNTD (reflecting recent evolutionary splits), significantly increased with experimentally manipulated tree species richness. Lepidopteran MNTD decreased with increasing tree MNTD. Path analyses showed that tree phylogenetic and functional diversity explained part, but not all of the effects of tree species richness on lepidopteran diversity. Importantly, tree diversity effects on lepidopteran diversity were to a large extent indirect, operating via changes in lepidopteran abundance. Synthesis. Our study shows that evolutionary dependencies determine the response of herbivore communities to changes in host plant diversity. Incorporating a wider range of diversity metrics both at the level of producers and consumers can thus help to develop a more comprehensive understanding of the functional consequences of biodiversity change across trophic levels. Moreover, the dependence of trophic linkages on herbivore abundances underlines the need to address the consequences of current declines in insect abundances for ecosystem structure and functioning.",
keywords = "BEF-China, biodiversity and ecosystem functioning, Hill numbers, Lepidoptera, phylogenetic diversity, plant species richness, Ecosystems Research",
author = "Ming-Qiang Wang and Yi Li and Douglas Chesters and Perttu Anttonen and Helge Bruelheide and Jing-Ting Chen and Walter Durka and Peng-Fei Guo and Werner Haerdtle and Keping Ma and Michalski, {Stefan G.} and Bernhard Schmid and {von Oheimb}, Goddert and Chun-Sheng Wu and Nai-Li Zhang and Qing-Song Zhou and Andreas Schuldt and Chao-Dong Zhu",
note = "Funding Information: We are grateful to the BEF‐China consortium for support (especially, Bo Yang, Shan Li and Xiao‐Juan Liu). We thank Ren‐Jie Zhang and several local assistants for their helps in the sampling. The authors particularly thank Maria Heikkil{\"a} (Finnish Museum of Natural History, Zoology Unit, University of Helsinki) for providing a nexus file of the backbone tree. We are grateful to Wenzel Kr{\"o}ber for the assessment of tree traits. This work was supported by the Strategic Priority Research Program of the Chinese Academy of Science (XDB310304) and the National Science Fund for Distinguished Young Scholars (31625024). We acknowledge funding of the BEF‐China experiment by the German Research Foundation (DFG FOR 891‐3 and 319936945/GRK2324). Ming‐Qiang Wang was supported by the UCAS Joint Ph.D. program (UCAS [2017‐26]) to study for 1 year at Andreas Schuldt's Lab, Georg‐August‐University of G{\"o}ttingen. H.B. acknowledges the support of the German Centre for Integrative Biodiversity Research (iDiv) Halle‐Jena‐Leipzig. B.S. was supported by the University Research Priority Program {\textquoteleft}Global Change and Biodiversity{\textquoteright} of the University of Zurich. D.C. was supported by the National Science Foundation of China (31772495). Publisher Copyright: {\textcopyright} 2019 The Authors. Journal of Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society.",
year = "2019",
month = nov,
day = "1",
doi = "10.1111/1365-2745.13273",
language = "English",
volume = "107",
pages = "2697--2712",
journal = "Journal of Ecology",
issn = "0022-0477",
publisher = "Wiley-Blackwell Publishing Ltd.",
number = "6",

}

RIS

TY - JOUR

T1 - Multiple components of plant diversity loss determine herbivore phylogenetic diversity in a subtropical forest experiment

AU - Wang, Ming-Qiang

AU - Li, Yi

AU - Chesters, Douglas

AU - Anttonen, Perttu

AU - Bruelheide, Helge

AU - Chen, Jing-Ting

AU - Durka, Walter

AU - Guo, Peng-Fei

AU - Haerdtle, Werner

AU - Ma, Keping

AU - Michalski, Stefan G.

AU - Schmid, Bernhard

AU - von Oheimb, Goddert

AU - Wu, Chun-Sheng

AU - Zhang, Nai-Li

AU - Zhou, Qing-Song

AU - Schuldt, Andreas

AU - Zhu, Chao-Dong

N1 - Funding Information: We are grateful to the BEF‐China consortium for support (especially, Bo Yang, Shan Li and Xiao‐Juan Liu). We thank Ren‐Jie Zhang and several local assistants for their helps in the sampling. The authors particularly thank Maria Heikkilä (Finnish Museum of Natural History, Zoology Unit, University of Helsinki) for providing a nexus file of the backbone tree. We are grateful to Wenzel Kröber for the assessment of tree traits. This work was supported by the Strategic Priority Research Program of the Chinese Academy of Science (XDB310304) and the National Science Fund for Distinguished Young Scholars (31625024). We acknowledge funding of the BEF‐China experiment by the German Research Foundation (DFG FOR 891‐3 and 319936945/GRK2324). Ming‐Qiang Wang was supported by the UCAS Joint Ph.D. program (UCAS [2017‐26]) to study for 1 year at Andreas Schuldt's Lab, Georg‐August‐University of Göttingen. H.B. acknowledges the support of the German Centre for Integrative Biodiversity Research (iDiv) Halle‐Jena‐Leipzig. B.S. was supported by the University Research Priority Program ‘Global Change and Biodiversity’ of the University of Zurich. D.C. was supported by the National Science Foundation of China (31772495). Publisher Copyright: © 2019 The Authors. Journal of Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society.

PY - 2019/11/1

Y1 - 2019/11/1

N2 - Plant diversity loss can alter higher trophic‐level communities via non‐random species interactions, which in turn may cascade to affect key ecosystem functions. These non‐random linkages might be best captured by patterns of phylogenetic diversity, which take into account co‐evolutionary dependencies. However, lack of adequate phylogenetic data of higher trophic levels hampers our mechanistic understanding of biodiversity relationships in species‐rich ecosystems. We used DNA barcoding to generate data on the phylogenetic diversity of lepidopteran caterpillars in a large‐scale forest biodiversity experiment in subtropical China. We analysed how different metrics of lepidopteran phylogenetic diversity (Faith's PD, MPD, MNTD) and taxonomic diversity were influenced by multiple components of tree diversity (taxonomic, functional, phylogenetic). Our data from six sampling periods represent 7,204 mitochondrial cytochrome c oxidase subunit I (COI) sequences of lepidopteran larvae, clustered into 461 molecular operational taxonomic units. Lepidopteran abundance, the effective number of species (irrespective of the focus on rare or common species) and Faith's PD and MPD (reflecting basal evolutionary splits), but not MNTD (reflecting recent evolutionary splits), significantly increased with experimentally manipulated tree species richness. Lepidopteran MNTD decreased with increasing tree MNTD. Path analyses showed that tree phylogenetic and functional diversity explained part, but not all of the effects of tree species richness on lepidopteran diversity. Importantly, tree diversity effects on lepidopteran diversity were to a large extent indirect, operating via changes in lepidopteran abundance. Synthesis. Our study shows that evolutionary dependencies determine the response of herbivore communities to changes in host plant diversity. Incorporating a wider range of diversity metrics both at the level of producers and consumers can thus help to develop a more comprehensive understanding of the functional consequences of biodiversity change across trophic levels. Moreover, the dependence of trophic linkages on herbivore abundances underlines the need to address the consequences of current declines in insect abundances for ecosystem structure and functioning.

AB - Plant diversity loss can alter higher trophic‐level communities via non‐random species interactions, which in turn may cascade to affect key ecosystem functions. These non‐random linkages might be best captured by patterns of phylogenetic diversity, which take into account co‐evolutionary dependencies. However, lack of adequate phylogenetic data of higher trophic levels hampers our mechanistic understanding of biodiversity relationships in species‐rich ecosystems. We used DNA barcoding to generate data on the phylogenetic diversity of lepidopteran caterpillars in a large‐scale forest biodiversity experiment in subtropical China. We analysed how different metrics of lepidopteran phylogenetic diversity (Faith's PD, MPD, MNTD) and taxonomic diversity were influenced by multiple components of tree diversity (taxonomic, functional, phylogenetic). Our data from six sampling periods represent 7,204 mitochondrial cytochrome c oxidase subunit I (COI) sequences of lepidopteran larvae, clustered into 461 molecular operational taxonomic units. Lepidopteran abundance, the effective number of species (irrespective of the focus on rare or common species) and Faith's PD and MPD (reflecting basal evolutionary splits), but not MNTD (reflecting recent evolutionary splits), significantly increased with experimentally manipulated tree species richness. Lepidopteran MNTD decreased with increasing tree MNTD. Path analyses showed that tree phylogenetic and functional diversity explained part, but not all of the effects of tree species richness on lepidopteran diversity. Importantly, tree diversity effects on lepidopteran diversity were to a large extent indirect, operating via changes in lepidopteran abundance. Synthesis. Our study shows that evolutionary dependencies determine the response of herbivore communities to changes in host plant diversity. Incorporating a wider range of diversity metrics both at the level of producers and consumers can thus help to develop a more comprehensive understanding of the functional consequences of biodiversity change across trophic levels. Moreover, the dependence of trophic linkages on herbivore abundances underlines the need to address the consequences of current declines in insect abundances for ecosystem structure and functioning.

KW - BEF-China

KW - biodiversity and ecosystem functioning

KW - Hill numbers

KW - Lepidoptera

KW - phylogenetic diversity

KW - plant species richness

KW - Ecosystems Research

UR - http://www.scopus.com/inward/record.url?scp=85073613889&partnerID=8YFLogxK

U2 - 10.1111/1365-2745.13273

DO - 10.1111/1365-2745.13273

M3 - Journal articles

VL - 107

SP - 2697

EP - 2712

JO - Journal of Ecology

JF - Journal of Ecology

SN - 0022-0477

IS - 6

ER -

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