Host-associated genetic divergence and taxonomy in the Rhinusa pilosa Gyllenhal species complex: an integrative approach
Authorized Users Only
2015
Authors
Toševski, Ivo
Caldara, Roberto
Jović, Jelena

Hernandez-Vera, Gerardo

Baviera, Cosimo
Gassmann, Andre
Emerson, Brent C.

Article (Published version)

Metadata
Show full item recordAbstract
A combined taxonomic, morphological, molecular and biological study revealed that stem-galling weevils from the genus Rhinusa associated with toadflaxes from the genus Linaria (Plantaginaceae) are composed of three different species: Rhinusa pilosa, Rhinusa brondelii and Rhinusa rarasp.n. The authentic field host plants are respectively, Linaria vulgaris, Linaria purpurea and Linaria genistifolia/ Linaria dalmatica. These weevil species can be distinguished from each other by a few subtle morphological characteristics, mainly in the shape of the rostrum and of the integument. An analysis of the mitochondrial [cytochrome oxidase subunit II gene (COII) and 16S ribosomal RNA gene (16S)] and nuclear (elongation factor-1, EF-1) sequence data revealed high genetic divergence among these species. Uncorrected pairwise distances on mtCOII gene were 14.3% between R. pilosa and R. brondelii, 15.7% between R. pilosa and R. rara, while R. brondelii and R. rara were approximately 11% divergent from ...each other. Divergences obtained on 16S and nuclear EF-1 genes were congruent. However, substantial intraspecific mitochondrial divergence was recorded for all studied populations of R. pilosa s.s. showing two mtDNA lineages, with estimated COII and 16S divergences of 4% and 1.6%, respectively. Nuclear pseudogenes (Numts) and Wolbachia influence, although recorded within both lineages, were excluded as possible causatives of the mtDNA divergence, while EF-1 indicated absence of lineage sorting. Species from the R. pilosa complex are estimated to have diverged from each other approximately 7.2 million years ago (mya; late Miocene), while R. brondelii and R. rara diverged from each other about 4.7 mya (early Pliocene). This published work has been registered in ZooBank, .
Source:
Systematic Entomology, 2015, 40, 1, 268-287Publisher:
- Wiley-Blackwell, Hoboken
Funding / projects:
- Wyoming Biological Control Steering Committee
- Ministry of Forests and Range
- British Columbia Provincial Government
- USDA-APHIS-CPHST
- USDA Forest Service through the Montana State University
- California Department of Food and Agriculture
- Agrobiodiversity and land-use change in Serbia: an integrated biodiversity assessment of key functional groups of arthropods and plant pathogens (RS-43001)
DOI: 10.1111/syen.12109
ISSN: 0307-6970
WoS: 000347453400016
Scopus: 2-s2.0-84920618643
Collections
Institution/Community
IZBISTY - JOUR AU - Toševski, Ivo AU - Caldara, Roberto AU - Jović, Jelena AU - Hernandez-Vera, Gerardo AU - Baviera, Cosimo AU - Gassmann, Andre AU - Emerson, Brent C. PY - 2015 UR - https://plantarum.izbis.bg.ac.rs/handle/123456789/395 AB - A combined taxonomic, morphological, molecular and biological study revealed that stem-galling weevils from the genus Rhinusa associated with toadflaxes from the genus Linaria (Plantaginaceae) are composed of three different species: Rhinusa pilosa, Rhinusa brondelii and Rhinusa rarasp.n. The authentic field host plants are respectively, Linaria vulgaris, Linaria purpurea and Linaria genistifolia/ Linaria dalmatica. These weevil species can be distinguished from each other by a few subtle morphological characteristics, mainly in the shape of the rostrum and of the integument. An analysis of the mitochondrial [cytochrome oxidase subunit II gene (COII) and 16S ribosomal RNA gene (16S)] and nuclear (elongation factor-1, EF-1) sequence data revealed high genetic divergence among these species. Uncorrected pairwise distances on mtCOII gene were 14.3% between R. pilosa and R. brondelii, 15.7% between R. pilosa and R. rara, while R. brondelii and R. rara were approximately 11% divergent from each other. Divergences obtained on 16S and nuclear EF-1 genes were congruent. However, substantial intraspecific mitochondrial divergence was recorded for all studied populations of R. pilosa s.s. showing two mtDNA lineages, with estimated COII and 16S divergences of 4% and 1.6%, respectively. Nuclear pseudogenes (Numts) and Wolbachia influence, although recorded within both lineages, were excluded as possible causatives of the mtDNA divergence, while EF-1 indicated absence of lineage sorting. Species from the R. pilosa complex are estimated to have diverged from each other approximately 7.2 million years ago (mya; late Miocene), while R. brondelii and R. rara diverged from each other about 4.7 mya (early Pliocene). This published work has been registered in ZooBank, . PB - Wiley-Blackwell, Hoboken T2 - Systematic Entomology T1 - Host-associated genetic divergence and taxonomy in the Rhinusa pilosa Gyllenhal species complex: an integrative approach EP - 287 IS - 1 SP - 268 VL - 40 DO - 10.1111/syen.12109 ER -
@article{ author = "Toševski, Ivo and Caldara, Roberto and Jović, Jelena and Hernandez-Vera, Gerardo and Baviera, Cosimo and Gassmann, Andre and Emerson, Brent C.", year = "2015", abstract = "A combined taxonomic, morphological, molecular and biological study revealed that stem-galling weevils from the genus Rhinusa associated with toadflaxes from the genus Linaria (Plantaginaceae) are composed of three different species: Rhinusa pilosa, Rhinusa brondelii and Rhinusa rarasp.n. The authentic field host plants are respectively, Linaria vulgaris, Linaria purpurea and Linaria genistifolia/ Linaria dalmatica. These weevil species can be distinguished from each other by a few subtle morphological characteristics, mainly in the shape of the rostrum and of the integument. An analysis of the mitochondrial [cytochrome oxidase subunit II gene (COII) and 16S ribosomal RNA gene (16S)] and nuclear (elongation factor-1, EF-1) sequence data revealed high genetic divergence among these species. Uncorrected pairwise distances on mtCOII gene were 14.3% between R. pilosa and R. brondelii, 15.7% between R. pilosa and R. rara, while R. brondelii and R. rara were approximately 11% divergent from each other. Divergences obtained on 16S and nuclear EF-1 genes were congruent. However, substantial intraspecific mitochondrial divergence was recorded for all studied populations of R. pilosa s.s. showing two mtDNA lineages, with estimated COII and 16S divergences of 4% and 1.6%, respectively. Nuclear pseudogenes (Numts) and Wolbachia influence, although recorded within both lineages, were excluded as possible causatives of the mtDNA divergence, while EF-1 indicated absence of lineage sorting. Species from the R. pilosa complex are estimated to have diverged from each other approximately 7.2 million years ago (mya; late Miocene), while R. brondelii and R. rara diverged from each other about 4.7 mya (early Pliocene). This published work has been registered in ZooBank, .", publisher = "Wiley-Blackwell, Hoboken", journal = "Systematic Entomology", title = "Host-associated genetic divergence and taxonomy in the Rhinusa pilosa Gyllenhal species complex: an integrative approach", pages = "287-268", number = "1", volume = "40", doi = "10.1111/syen.12109" }
Toševski, I., Caldara, R., Jović, J., Hernandez-Vera, G., Baviera, C., Gassmann, A.,& Emerson, B. C.. (2015). Host-associated genetic divergence and taxonomy in the Rhinusa pilosa Gyllenhal species complex: an integrative approach. in Systematic Entomology Wiley-Blackwell, Hoboken., 40(1), 268-287. https://doi.org/10.1111/syen.12109
Toševski I, Caldara R, Jović J, Hernandez-Vera G, Baviera C, Gassmann A, Emerson BC. Host-associated genetic divergence and taxonomy in the Rhinusa pilosa Gyllenhal species complex: an integrative approach. in Systematic Entomology. 2015;40(1):268-287. doi:10.1111/syen.12109 .
Toševski, Ivo, Caldara, Roberto, Jović, Jelena, Hernandez-Vera, Gerardo, Baviera, Cosimo, Gassmann, Andre, Emerson, Brent C., "Host-associated genetic divergence and taxonomy in the Rhinusa pilosa Gyllenhal species complex: an integrative approach" in Systematic Entomology, 40, no. 1 (2015):268-287, https://doi.org/10.1111/syen.12109 . .