Literature DB >> 29122650

Phylogeny, new generic-level classification, and historical biogeography of the Eucera complex (Hymenoptera: Apidae).

A Dorchin1, M M López-Uribe2, C J Praz3, T Griswold4, B N Danforth5.   

Abstract

The longhorn bee tribe Eucerini (Hymenoptera: Apidae) is a diverse, widely distributed group of solitary bees that includes important pollinators of both wild and agricultural plants. About half of the species in the tribe are currently assigned to the genus Eucera and to a few other related genera. In this large genus complex, comprising ca. 390 species, the boundaries between genera remain ambiguous due to morphological intergradation among taxa. Using ca. 6700 aligned nucleotide sites from six gene fragments, 120 morphological characters, and more than 100 taxa, we present the first comprehensive molecular, morphological, and combined phylogenetic analyses of the 'Eucera complex'. The revised generic classification that we propose is congruent with our phylogeny and maximizes both generic stability and ease of identification. Under this new classification most generic names are synonymized under an expanded genus Eucera. Thus, Tetralonia, Peponapis, Xenoglossa, Cemolobus, and Syntrichalonia are reduced to subgeneric rank within Eucera, and Synhalonia is retained as a subgenus of Eucera. Xenoglossodes is reestablished as a valid subgenus of Eucera while Tetraloniella is synonymized with Tetralonia and Cubitalia with Eucera. In contrast, we suggest that the venusta-group of species, currently placed in the subgenus Synhalonia, should be recognized as a new genus. Our results demonstrate the need to evaluate convergent loss or gain of important diagnostic traits to minimize the use of potentially homoplasious characters when establishing classifications. Lastly, we show that the Eucera complex originated in the Nearctic region in the late Oligocene, and dispersed twice into the Old World. The first dispersal event likely occurred 24.2-16.6 mya at a base of a clade of summer-active bees restricted to warm region of the Old World, and the second 13.9-12.3 mya at the base of a clade of spring-active bees found in cooler regions of the Holarctic. Our results further highlight the role of Beringia as a climate-regulated corridor for bees.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ancestral range construction; Bees; Beringia; Cladistics; Divergence time estimation; Homoplasy

Mesh:

Year:  2017        PMID: 29122650     DOI: 10.1016/j.ympev.2017.10.007

Source DB:  PubMed          Journal:  Mol Phylogenet Evol        ISSN: 1055-7903            Impact factor:   4.286


  3 in total

1.  Bee flowers drive macroevolutionary diversification in long-horned bees.

Authors:  Achik Dorchin; Anat Shafir; Frank H Neumann; Dafna Langgut; Nicolas J Vereecken; Itay Mayrose
Journal:  Proc Biol Sci       Date:  2021-09-22       Impact factor: 5.349

2.  A novel and non-invasive method for DNA extraction from dry bee specimens.

Authors:  Giovanni Cilia; Simone Flaminio; Marino Quaranta
Journal:  Sci Rep       Date:  2022-07-08       Impact factor: 4.996

3.  Partitioned Gene-Tree Analyses and Gene-Based Topology Testing Help Resolve Incongruence in a Phylogenomic Study of Host-Specialist Bees (Apidae: Eucerinae).

Authors:  Felipe V Freitas; Michael G Branstetter; Terry Griswold; Eduardo A B Almeida
Journal:  Mol Biol Evol       Date:  2021-03-09       Impact factor: 16.240

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.