Mariusz Kanturski

Dr. Mariusz Kanturski

Faculty of Natural Sciences, Institute of Biology, Biotechnology and Environmental Protection, University of Silesia in Katowice, Bankowa 9,40-007 Katowice, Poland
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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2015 in Micron
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Journal Article
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Mariusz KanturskiMariusz Kanturski
Mariusz Kanturski
JKJagna Karcz
Jagna Karcz
KWKarina Wieczorek
Karina Wieczorek

12 July 2020 in Biological Reviews
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Łukasz DepaŁukasz Depa
Łukasz Depa
NKNatalia Kaszyca‐Taszakowska
Natalia Kaszyca‐Taszakowska
Artur TaszakowskiArtur Taszakowski
Artur Taszakowski
Mariusz KanturskiMariusz Kanturski
Mariusz Kanturski

27 April 2017 in PLOS ONE
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YLYerim Lee
Yerim Lee
WLWonhoon Lee
Wonhoon Lee
Mariusz KanturskiMariusz Kanturski
Mariusz Kanturski
RFRobert G. Foottit
Robert G. Foottit
SAShin-Ichi Akimoto
Shin-Ichi Akimoto
SLSeunghwan Lee
Seunghwan Lee
Aphids are a species rich group comprising many important pests. However, species identification can be very difficult for aphids due to their morphological ambiguity. DNA barcoding has been widely adopted for rapid and reliable species identification as well as cryptic species detection. In this study, we investigated cryptic diversity in the subfamily Calaphidinae (Hemiptera: Aphididae) based on 899 sequences of cytochrome c oxidase I (COI) for 115 morphospecies (78 species collected in this study and sequences of 73 species downloaded from Genbank). Among these 115 morphospecies, DNA barcoding results of 90 (78.3%) species were identical to results of morphological identification. However, 25 (21.7%) morphospecies showed discrepancies between DNA barcoding and traditional taxonomy. Among these 25 discordances, a total of 15 cryptic species were identified from 12 morphospecies. We also found three morphologically distinct species pairs that sharing DNA barcoding. Based on molecular operational taxonomic unit (MOTU) estimation, we discussed on species delimitation threshold value for these taxa. Our findings confirm that Calaphidinae has high cryptic diversity even though aphids are relatively well-studied.

1 December 2015 in Polish Journal of Entomology
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MSMarzena Starowicz
Marzena Starowicz
Mariusz KanturskiMariusz Kanturski
Mariusz Kanturski
ŁJŁukasz Junkiert
Łukasz Junkiert
KWKarina Wieczorek
Karina Wieczorek
The paper presents results of faunistic investigations of aphids (Aphidomorpha) in the Botanic Garden of the Jagiellonian University, Kraków, in the Kraków – Wieluń Upland. During two seasons of research (2011, 2012) two aphid species from the family Adelgidae and 50 species from the family Aphididae, associated with 66 host plants were recorded. The following species – Eriosoma anncharlotteae Danielsson, 1979, Capitophorus elaeagni (Del Guercio, 1894), Rhopalosiphoninus (Neorhopalosiphoninus) staphyleae staphyleae (Koch, 1854), Eulachnus brevipilosus Börner, 1940 and E. cembrae Börner, 1950 – are new for the Kraków – Wieluń Upland. Seven of the species recorded are regarded as alien to Poland.

1 January 2017 in Zoologischer Anzeiger
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Journal Article
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Mariusz KanturskiMariusz Kanturski
Mariusz Kanturski
SAShahid Ali Akbar
Shahid Ali Akbar
CFColin Favret
Colin Favret

13 March 2017 in PLOS ONE
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KWKarina Wieczorek
Karina Wieczorek
DLDorota Lachowska-Cierlik
Dorota Lachowska-Cierlik
Lukasz KajtochLukasz Kajtoch
Lukasz Kajtoch
Mariusz KanturskiMariusz Kanturski
Mariusz Kanturski
The Chaitophorinae is a bionomically diverse Holarctic subfamily of Aphididae. The current classification includes two tribes: the Chaitophorini associated with deciduous trees and shrubs, and Siphini that feed on monocotyledonous plants. We present the first phylogenetic hypothesis for the subfamily, based on molecular and morphological datasets. Molecular analyses were based on the mitochondrial gene cytochrome oxidase subunit I (COI) and the nuclear gene elongation factor-1α (EF-1α). Phylogenetic inferences were obtained individually on each of genes and joined alignments using Bayesian inference (BI) and Maximum likelihood (ML). In phylogenetic trees reconstructed on the basis of nuclear and mitochondrial genes as well as a morphological dataset, the monophyly of Siphini and the genus Chaitophorus was supported. Periphyllus forms independent lineages from Chaitophorus and Siphini. Within this genus two clades comprising European and Asiatic species, respectively, were indicated. Concerning relationships within the subfamily, EF-1α and joined COI and EF-1α genes analysis strongly supports the hypothesis that Chaitophorini do not form a monophyletic clade. Periphyllus is a sister group to a clade containing Chaitophorus and Siphini. The Asiatic unit of Periphyllus also includes Trichaitophorus koyaensis. The analysis of morphological dataset under equally weighted parsimony also supports the view that Chaitophorini is an artificial taxon, as Lambersaphis pruinosae and Pseudopterocomma hughi, both traditionally included in the Chaitophorini, formed independent lineages. COI analyses support consistent groups within the subfamily, but relationships between groups are poorly resolved. These analyses were extended to include the species of closely related and phylogenetically unstudied subfamily Drepanosiphinae, which produced congruent results. Genera Drepanosiphum and Depanaphis are monophyletic and sister. The position of Yamatocallis tokyoensis differs in the molecular and morphological analyses, i.e. it is either an independent lineage (EF-1α, COI, joined COI and EF-1α genes) or is nested inside this unit (morphology). Our data also support separation of Chaitophorinae from Drepanosiphinae.