2012
DOI: 10.1016/j.soilbio.2012.03.020
|View full text |Cite
|
Sign up to set email alerts
|

Isolation of polymorphic microsatellite markers in Aporrectodea icterica (Savigny 1826)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
20
0

Year Published

2013
2013
2020
2020

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 14 publications
(21 citation statements)
references
References 18 publications
1
20
0
Order By: Relevance
“…For instance, the number of alleles was three times higher for A. chlorotica than for A. icterica. This difference is not a particularity of the study because the level of genetic diversity recorded is similar to the results of Dupont et al (2011) for A. chlorotica and of Torres-Leguizamon et al (2012) and Torres-Leguizamon et al (2014) for A. icterica at the landscape/region scale. In our study, A. icterica Table 2.…”
Section: Spatial Genetic Structure Of Earthworms 341 Discussionsupporting
confidence: 54%
See 3 more Smart Citations
“…For instance, the number of alleles was three times higher for A. chlorotica than for A. icterica. This difference is not a particularity of the study because the level of genetic diversity recorded is similar to the results of Dupont et al (2011) for A. chlorotica and of Torres-Leguizamon et al (2012) and Torres-Leguizamon et al (2014) for A. icterica at the landscape/region scale. In our study, A. icterica Table 2.…”
Section: Spatial Genetic Structure Of Earthworms 341 Discussionsupporting
confidence: 54%
“…Its taxonomic status is firmly grounded and the species has distinct morphology, making it easy to recognize (Torres- Leguizamon et al, 2012). Conversely, the A. chlorotica aggregate (Dupont et al, 2011) is composed of several sister species.…”
Section: Biological Modelsmentioning
confidence: 99%
See 2 more Smart Citations
“…For the I20 and IR populations, sequences were taken from Torres-Leguizamon et al [27] (GenBank accession numbers JN381881–JN381930). Each amplification mixture (25 µl) contained 10 ng DNA, 12.5 µl of Taq PCR Master Mix (Qiagen, Hilden, Germany) and 0.25 µM of each primer.…”
Section: Methodsmentioning
confidence: 99%