Evidence map›Paper›PMID 36994537›Full record

ArticleZoological research2023

Evolutionary timescale of chalcidoid wasps inferred from over one hundred mitochondrial genomes.

Jia-Chen Zhu, Hui Xiao, Pu Tang, Xiao-Fei Li, Xuan-Kun Li, Chao-Dong Zhu, Qiong Wu, Jin-Hua Xiao, Cornelis van Achterberg, Da-Wei Huang and 1 more

Abstract read
In one paragraph

Article in Zoological research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jia-Chen ZhuState Key Laboratory of Rice Biology, Ministry of Agriculture and Rural Affairs Key Lab of Molecular Biology of Crop Pathogens and Insect Pests, Provincial Key Lab of Biology of Crop Pathogens and Insect Pests of Zhejiang, Institute of Insect Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Hui XiaoKey Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Pu TangState Key Laboratory of Rice Biology, Ministry of Agriculture and Rural Affairs Key Lab of Molecular Biology of Crop Pathogens and Insect Pests, Provincial Key Lab of Biology of Crop Pathogens and Insect Pests of Zhejiang, Institute of Insect Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Xiao-Fei LiState Key Laboratory of Rice Biology, Ministry of Agriculture and Rural Affairs Key Lab of Molecular Biology of Crop Pathogens and Insect Pests, Provincial Key Lab of Biology of Crop Pathogens and Insect Pests of Zhejiang, Institute of Insect Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Xuan-Kun LiFlorida Museum of Natural History, University of Florida, Gainesville, FL 32611 USA.
Chao-Dong ZhuKey Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Qiong WuState Key Laboratory of Rice Biology, Ministry of Agriculture and Rural Affairs Key Lab of Molecular Biology of Crop Pathogens and Insect Pests, Provincial Key Lab of Biology of Crop Pathogens and Insect Pests of Zhejiang, Institute of Insect Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Jin-Hua XiaoCollege of Life Sciences, Nankai University, Tianjin 300071, China.
Cornelis van AchterbergState Key Laboratory of Rice Biology, Ministry of Agriculture and Rural Affairs Key Lab of Molecular Biology of Crop Pathogens and Insect Pests, Provincial Key Lab of Biology of Crop Pathogens and Insect Pests of Zhejiang, Institute of Insect Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Da-Wei HuangCollege of Life Sciences, Nankai University, Tianjin 300071, China.
Xue-Xin ChenState Key Laboratory of Rice Biology, Ministry of Agriculture and Rural Affairs Key Lab of Molecular Biology of Crop Pathogens and Insect Pests, Provincial Key Lab of Biology of Crop Pathogens and Insect Pests of Zhejiang, Institute of Insect Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China. E-mail: xxchen@zju.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chalcidoidea is one of the most biologically diverse groups among Hymenoptera. Members are characterized by extraordinary parasitic lifestyles and extensive host ranges, among which several species attack plants or serve as pollinators. However, higher-level chalcidoid relationships remain controversial. Here, we performed mitochondrial phylogenomic analyses for major clades (18 out of 25 families) of Chalcidoidea based on 139 mitochondrial genomes. The compositional heterogeneity and conflicting backbone relationships in Chalcidoidea were assessed using various datasets and tree inferences. Our phylogenetic results supported the monophyly of 16 families and polyphyly of Aphelinidae and Pteromalidae. Our preferred topology recovered the relationship (Mymaridae+(Signiphoridae+Leucospidae)+(Chalcididae+((Perilampidae+Eucharitidae)+ remaining Chalcidoidea)))). The monophyly of Agaonidae and Sycophaginae was rejected, while the gall-associated ((Megastigmidae+Ormyridae)+(Ormocerinae+Eurytomidae)) relationship was supported in most results. A six-gene inversion may be a synapomorphy for most families, whereas other derived gene orders may introduce confusion in phylogenetic signals at deeper nodes. Dating estimates suggested that Chalcidoidea arose near the Jurassic/Cretaceous boundary and that two dynamic shifts in diversification occurred during the evolution of Chalcidoidea. We hypothesized that the potential codiversification between chalcidoids and their hosts may be crucial for accelerating the diversification of Chalcidoidea. Ancestral state reconstruction analyses supported the hypothesis that gall-inducers were mainly derived from parasitoids of gall-inducers, while other gall-inducers were derived from phytophagous groups. Taken together, these findings advance our understanding of mitochondrial genome evolution in the major interfamilial phylogeny of Chalcidoidea.

Indexed as

Genome, MitochondrialWaspsAnimalsPhylogenyChalcidoideaCompositional heterogeneityDivergence timeEvolution of host and gall associationsMitochondrial genome

Identifiers

PMID36994537
PMCPMC10236298

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.