Erratum to: Microsatellite records for volume 7, issue 4

Abstract

In the original publication of the article, the author group was published incorrectly. The correct author group is given in this erratum.

The role of environment and core‐margin effects on range‐wide phenotypic variation in a montane grasshopper

“…All individuals were genotyped at 18 polymorphic microsatellites markers whose characteristics and PCR cycling conditions are detailed in Basiita et al . (). We performed PCR amplifications and genotyping following the procedure described in Ortego et al .…”

Testing the role of ancient and contemporary landscapes on structuring genetic variation in a specialist grasshopper

“…We extracted genomic DNA from a hind leg of each individual using a salt extraction protocol (Aljanabi & Martinez, ). Each individual was genotyped at 18 species‐specific microsatellites markers (Basiita et al., ). All microsatellite markers were polymorphic in all populations, and the most common alleles were shared across all populations.…”

“…We performed PCRs and genotyping following the procedure described in Ortego, Aguirre, Noguerales, and Cordero () and Basiita et al. (). We tested for deviations from Hardy–Weinberg equilibrium, linkage disequilibrium (LD), and the presence of null alleles as described in Noguerales, Cordero, and Ortego ().…”

Hidden in plain view: Cryptic diversity in the emblematic Araucaria of New Caledonia

“…PCR amplifi cation -Genetic differentiation was assessed using 14 plastid and 12 nuclear microsatellites (SSRs) ( Goossens, 2015 ;Basiita et al, 2016 ), as well as a 317 bp long section of the psbA-trnH intergenic spacer containing a variable 13 bp minisatellite motif (AGTCTAGATTTAG). PCR protocol and amplifi cation of the SSRs followed Basiita et al (2016) .…”

“…PCR amplifi cation -Genetic differentiation was assessed using 14 plastid and 12 nuclear microsatellites (SSRs) ( Goossens, 2015 ;Basiita et al, 2016 ), as well as a 317 bp long section of the psbA-trnH intergenic spacer containing a variable 13 bp minisatellite motif (AGTCTAGATTTAG). PCR protocol and amplifi cation of the SSRs followed Basiita et al (2016) . Th e minisatellite was amplifi ed in volumes of 10 μ L using the following protocol: 1 × PCR buff er (Bioline, London, UK), 0.2 mM dNTP (Bioline, London, UK), 2.5 mM MgCl 2 , 0.2 μM forward (5 ′ -6FAM-CC-GATGGATTGTTAGTGTGT-3 ′ ) and reverse primer (5 ′ -TTCTAT-GATTTAGAAGAGTCC-3 ′ ), 0.025 units Bio Taq (Bioline, London, UK) and 1 μL of unquantified DNA.…”