2017
DOI: 10.5817/mab2017-16-37
|View full text |Cite
|
Sign up to set email alerts
|

First record of Trochulus clandestinus (Hartmann, 1821) in Austria (Gastropoda: Eupulmonata: Hygromiidae)

Abstract: The north-west alpine distributed hairy snail Trochulus clandestinus (Hartmann, 1821) was recorded for the first time from Austria. Two living specimens were found in Vorarlberg 11 July 2016. The animals were subjected to genetic barcoding and their genital organs were dissected. The taxonomic situation within north-west alpine species of the genus Trochulus is not unambiguously resolved, but the assignment of the Austrian specimens as T. clandestinus is the most reliable at the current state of knowledge. The… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
5

Relationship

2
3

Authors

Journals

citations
Cited by 6 publications
(2 citation statements)
references
References 12 publications
0
2
0
Order By: Relevance
“…Full-length COI-5P DNA barcodes were amplified using primer sets LCO1490/ HCO2198 [44] and jgLCO1490/jgHCO2198 [45]. Even though additional primer sets were initially tested [46,47], all DNA barcodes were successfully amplified with the use of jgLCO1490/jgHCO2198 primer set with the exception of the specimens identified as Mytilus galloprovincialis which were amplified with LCO1490/HCO2198 primer set. 20 µL polymerase chain reactions (PCR) mixture contained 1× DreamTaq TM Reaction Buffer (containing 2 mM MgCl 2 , Thermo Scientific, Waltham, Massachusetts, USA), 0.2 mM dNTP mix (Qiagen), 0.5 µM of each primer, 1.0 U DreamTaq polymerase (Thermo Scientific) and 3 µL of DNA eluate (10-fold dilution of the second eluate).…”
Section: Methodsmentioning
confidence: 99%
“…Full-length COI-5P DNA barcodes were amplified using primer sets LCO1490/ HCO2198 [44] and jgLCO1490/jgHCO2198 [45]. Even though additional primer sets were initially tested [46,47], all DNA barcodes were successfully amplified with the use of jgLCO1490/jgHCO2198 primer set with the exception of the specimens identified as Mytilus galloprovincialis which were amplified with LCO1490/HCO2198 primer set. 20 µL polymerase chain reactions (PCR) mixture contained 1× DreamTaq TM Reaction Buffer (containing 2 mM MgCl 2 , Thermo Scientific, Waltham, Massachusetts, USA), 0.2 mM dNTP mix (Qiagen), 0.5 µM of each primer, 1.0 U DreamTaq polymerase (Thermo Scientific) and 3 µL of DNA eluate (10-fold dilution of the second eluate).…”
Section: Methodsmentioning
confidence: 99%
“…The Qubit TM dsDNA HS Assay Kit with the associated standard protocol was used. To amplify the DNA barcoding fragment of the mitochondrial cytochrome oxidase 1 gene, the primer pair LCO1490_Mol1/HCO2198_Mol1 (Duda et al, 2017) was used. PCRs were performed on a Master Gradient thermocycler (Eppendorf) in 25 ml elution buffer with 5 ml template DNA, using the QIAGEN Multiplex PCR Kit with 0.5 mM of each primer.…”
Section: Methodsmentioning
confidence: 99%