Isolation and characterization of microsatellite DNA loci from the golden cuttlefish,Sepia esculenta Hoyle (Cephalopoda)

The first microsatellite markers were isolated from the golden cuttlefish, Sepia esculenta Hoyle. Eleven primer sets were designed to amplify the marker sequences via polymerase chain reaction. The 45–50 individuals from one wild population in the coastal waters of Ehime Prefecture, Japan were used to screen polymorphism in the 11 microsatellite loci. All the microsatellite loci were polymorphic, with the range of alleles from seven to 27 per locus. The observed and expected heterozygosities ranged from 0.380 to 0.980 and from 0.654 to 0.940, respectively. These marker loci except for one locus showing significant deviation from Hardy–Weinberg equilibrium will be useful for the assessment of genetic variation and population structure of this species.     

Isolation of polymorphic tri- and tetranucleotide microsatellite loci for the highly endangered Baw Baw frog (Philoria frosti)

We isolated 15 polymorphic microsatellite loci for the Baw Baw frog, Philoria frosti, from a genomic library enriched for (AAC)(n) and (AAAG)(n) repetitive elements. The number of alleles ranges from two to 14 per locus with the observed heterozygosity ranging from 0.04 to 0.96.     

Isolation of polymorphic tetranucleotide microsatellite markers for the large‐billed scrubwren (Sericornis magnirostris)

We isolated 12 polymorphic microsatellite markers for the large‐billed scrubwren Sericornis magnirostris from genomic libraries enriched for (AAGG)_n and (AACC)_n repetitive elements and characterized them in 11 individuals. The number of alleles ranged from four to 15 per locus with the observed heterozygosity ranging from 0.14 to 0.91. These markers will be useful to address questions concerning population genetic structure and models of speciation.     

Isolation of polymorphic tetranucleotide microsatellite markers for the black‐bellied seedcracker (Pyrenestes ostrinus)

We have isolated 10 polymorphic microsatellite markers for the black‐bellied seedcracker (Pyrenestes ostrinus) from genomic libraries enriched either for (AAGG)_n or (ATCT)_n repetitive elements and characterized them in 39 individuals. The number of alleles ranged from two to 27 per locus with the observed heterozygosity ranging from 0.38 to 0.94. These markers will be useful for analysis of questions concerning parentage and population genetic structure.     

Isolation of polymorphic tetranucleotide microsatellite markers for the grey‐headed robin (Poecilodryas albispecularis)

We isolated 12 polymorphic microsatellite markers for the grey‐headed robin Poecilodryas albispecularis from genomic libraries enriched for (AAGG)n and (AACC)n repetitive elements and characterized them in 12 individuals. The number of alleles ranges from three to nine per locus with the observed heterozygosity ranging from 0.33 to 0.90. These markers will be useful for analysis of questions concerning population genetic structure and testing models of speciation.     

Isolation of polymorphic tetranucleotide microsatellite markers for the brown anole (Anolis sagrei)

Eleven polymorphic microsatellite markers have been developed for the brown anole, Anolis sagrei. The number of alleles range from five to 14 per locus with the observed heterozygosity ranging from 0.46 to 0.92. These markers will be useful for analysis of questions concerning population genetic structure and reproductive behaviour.     

Isolation of polymorphic tetranucleotide microsatellite markers for the green‐eyed tree frog (Litoria genimaculata)

We have isolated 16 polymorphic microsatellite markers for the green‐eyed tree frog, Litoria genimaculata, from genomic libraries enriched for (AAGG)_n and (AAAG)_n repetitive elements. The number of alleles ranges from four to 14 per locus with the observed heterozygosity ranging from 0.36 to 1.00. These markers will be useful for analysis of questions concerning population genetic structure and speciation.     

Isolation of polymorphic tetranucleotide microsatellite markers for the little greenbul (Andropadus virens)

Thirteen polymorphic microsatellite markers have been developed for the little greenbul, Andropadus virens. The number of alleles range from two to 15 per locus with the observed heterozygosity ranging from 0.15 to 0.92. Eight sets of primers also amplify in closely related species, Andropadus laterostris and Andropadus tephrolaemus. These markers will be useful for analysis of questions concerning population genetic structure and models of speciation.     

Isolation of polymorphic tetranucleotide microsatellite markers for the silky short‐tailed bat Carollia brevicauda

We isolated 10 polymorphic microsatellite markers for the silky short‐tailed bat, Carollia brevicauda, from genomic libraries enriched for (AAGG)_n repetitive elements. The number of alleles ranged from six to 25 per locus with the observed heterozygosity ranging from 0.29 to 0.95. These markers will be useful for analysis of questions concerning population genetic structure and models of speciation. Results of cross‐species amplification in Carollia castanea and Carollia perspicillata are also reported.     

Isolation of polymorphic tetranucleotide microsatellite markers for the skink Mabuya affinis

We isolated 10 polymorphic microsatellite markers for the skink Mabuya affinis from genomic libraries enriched for (AAGG)_n and (AAAG)_n repetitive elements. The number of alleles ranged from eight to 13 per locus with the observed heterozygosity ranging from 0.60 to 0.92. These markers will be useful for analysis of questions concerning population genetic structure and models of speciation.     

Isolation of polymorphic tetranucleotide microsatellite markers for the wedge‐billed woodcreeper Glyphorynchus spirurus

We have isolated six polymorphic microsatellite markers for the wedge‐billed woodcreeper Glyphorynchus spirurus from a genomic library enriched for (AAGG)_n repetitive elements, and characterized them in 25 individuals. The number of alleles ranged from eight to 20 per locus, with observed heterozygosity ranging from 0.43 to 0.78.     

Isolation of polymorphic tetranucleotide microsatellite markers for the streak‐necked flycatcher Mionectes striaticollis

We have isolated 11 polymorphic microsatellite markers for the streak‐necked flycatcher Mionectes striaticollis from genomic libraries enriched for either (AACC)_n, (AAGG)_n or (AAAG)_n repetitive elements. The number of alleles ranged from four to 14 per locus with the observed heterozygosity ranging from 0.38 to 1.00. These markers will be useful for analysis of questions concerning population genetic structure and models of speciation.     

Isolation of polymorphic tetranucleotide microsatellite markers for the bay pipefish Syngnathus leptorhynchus

We have isolated nine polymorphic microsatellite markers for the bay pipefish Syngnathus leptorhynchus from genomic libraries enriched for (AAGG)_n repetitive elements. The number of alleles ranged from two to 15 per locus with the observed heterozygosity ranging from 0.09 to 1.00. These markers will be useful for analyses of questions concerning population genetic structure.     

Isolation of polymorphic tetranucleotide microsatellite markers for the pygmy kingfisher Ceyx picta

We have isolated 13 polymorphic microsatellite markers for the pygmy kingfisher, Ceyx picta, from genomic libraries enriched for either (AAGG)_n or (AACC)_n repetitive elements. The number of alleles range from three to 15 per locus with an observed heterozygosity ranging from 0.46 to 1.00. These markers will be useful for analysis of questions concerning population genetic structure and models of speciation.     

Isolation and characterization of polymorphic tetranucleotide microsatellite loci in the Fire salamander Salamandra salamandra (Amphibia: Caudata)

Ten tetranucleotide and one dinucleotide polymorphic microsatellite loci were cloned and characterized for the Fire salamander (Salamandra salamandra) from 34 populations in Germany. A high genetic diversity (5–22 alleles per locus) and heterozygosity (40.6–95.2%) were observed for these markers. Chord distances for population comparisons of the western evolutionary recolonization lineage in the area near Cologne ranged from 0.139 to 0.366, whereas population comparisons between the western and eastern lineage ranged from 0.541 to 0.670. When compared with classical isolation methods, a sufficient number of polymorphic microsatellites can be obtained for the Fire salamander only from specially enriched sublibraries.     

Di‐, tri‐ and tetranucleotide microsatellite loci for the giant panda,Ailuropoda melanoleuca

We describe 10 polymorphic microsatellite loci for the giant panda, Ailuropoda melanoleuca. Microsatellite sequences were isolated from three partial genomic libraries of giant panda DNA that were enriched for (i) (GT), (ii) (GAA) & (CAA), and (iii) (GATA) repeat sequences. The markers were tested for polymorphism in up to 82 pandas. Number of alleles at each locus varied between four and 11, and the observed and expected heterozygosities varied between 0.267 and 0.732, and between 0.601 and 0.799, respectively.     

Isolation of polymorphic tetranucleotide microsatellite markers for the masked flowerpiercer Diglossa cyanea

We have isolated 11 polymorphic microsatellite markers for the masked flowerpiercer Diglossa cyanea from a genomic library enriched for (AAGG)_n repetitive elements. The number of alleles ranged from eight to 16 per locus with the observed heterozygosity ranging from 0.64 to 1.00. These markers will be useful for analysis of questions concerning population genetic structure and models of speciation.     

Isolation of polymorphic tetranucleotide microsatellite markers for the ornate nursery frog Cophixalus ornatus

We have isolated 18 polymorphic microsatellite loci for Cophixalus ornatus from genomic libraries enriched for (AAAG)_n, (AACC)_n and (AAGG)_n repetitive elements. The number of alleles ranges from five to 22 per locus with the observed heterozygosity ranging from 0.10 to 0.92. These markers will be useful for the analysis of population structure in C. ornatus and testing alternative models of speciation.