No abstract

This article documents the addition of 512 microsatellite marker loci and nine pairs of Single Nucleotide Polymorphism (SNP) sequencing primers to the Molecular Ecology Resources Database. Loci were developed for the following species: Alcippe morrisonia morrisonia, Bashania fangiana, Bashania fargesii, Chaetodon vagabundus, Colletes floralis, Coluber constrictor flaviventris, Coptotermes gestroi, Crotophaga major, Cyprinella lutrensis, Danaus plexippus, Fagus grandifolia, Falco tinnunculus, Fletcherimyia fletcheri, Hydrilla verticillata, Laterallus jamaicensis coturniculus, Leavenworthia alabamica, Marmosops incanus, Miichthys miiuy, Nasua nasua, Noturus exilis, Odontesthes bonariensis, Quadrula fragosa, Pinctada maxima, Pseudaletia separata, Pseudoperonospora cubensis, Podocarpus elatus, Portunus trituberculatus, Rhagoletis cerasi, Rhinella schneideri, Sarracenia alata, Skeletonema marinoi, Sminthurus viridis, Syngnathus abaster, Uroteuthis (Photololigo) chinensis, Verticillium dahliae, Wasmannia auropunctata, and Zygochlamys patagonica. These loci were cross-tested on the following species: Chaetodon baronessa, Falco columbarius, Falco eleonorae, Falco naumanni, Falco peregrinus, Falco subbuteo, Didelphis aurita, Gracilinanus microtarsus, Marmosops paulensis, Monodelphis Americana, Odontesthes hatcheri, Podocarpus grayi, Podocarpus lawrencei, Podocarpus smithii, Portunus pelagicus, Syngnathus acus, Syngnathus typhle,Uroteuthis (Photololigo) edulis, Uroteuthis (Photololigo) duvauceli and Verticillium albo-atrum. This article also documents the addition of nine sequencing primer pairs and sixteen allele specific primers or probes for Oncorhynchus mykiss and Oncorhynchus tshawytscha; these primers and assays were cross-tested in both species.

This article documents the addition of 238 microsatellite marker loci to the Molecular Ecology Resources Database. Loci were developed for the following species: Alytes dickhilleni, Arapaima gigas, Austropotamobius italicus, Blumeria graminis f. sp. tritici, Cobitis lutheri, Dendroctonus ponderosae, Glossina morsitans morsitans, Haplophilus subterraneus, Kirengeshoma palmata, Lysimachia japonica, Macrolophus pygmaeus, Microtus cabrerae, Mytilus galloprovincialis, Pallisentis (Neosentis) celatus, Pulmonaria officinalis, Salminus franciscanus, Thais chocolata and Zootoca vivipara. These loci were cross-tested on the following species: Acanthina monodon, Alytes cisternasii, Alytes maurus, Alytes muletensis, Alytes obstetricans almogavarii, Alytes obstetricans boscai, Alytes obstetricans obstetricans, Alytes obstetricans pertinax, Cambarellus montezumae, Cambarellus zempoalensis, Chorus giganteus, Cobitis tetralineata, Glossina fuscipes fuscipes, Glossina pallidipes, Lysimachia japonica var. japonica, Lysimachia japonica var. minutissima, Orconectes virilis, Pacifastacus leniusculus, Procambarus clarkii, Salminus brasiliensis and Salminus hilarii.

In low-energy salt-marsh environments, Fucus spp. frequently exhibit an atypical morphology that is characterized by the absence of an anchoring holdfast and a trend towards reduced size and buoyancy, enhanced vegetative proliferation, and often the loss of sexual reproduction. Such forms, often referred to as ecads, presumably derive from typical attached forms, but their affinities are normally difficult to establish with confidence due to their simplified and largely convergent morphology. Minute salt-marsh forms growing partially embedded in the sediment occur on Atlantic and Pacific coasts and have traditionally been recognized as an independent entity, Fucus cottonii. In this study we analyse with four microsatellite loci two F. cottonii populations from salt-marshes of Oregon (NE Pacific) and Ireland (Europe, near the species type locality), as well as local populations of other Fucus spp. that could be considered potential source populations, either directly or via hybridization. Our results show that the F. cottonii from Oregon derive from F. gardneri whereas the Irish population is closer to F. spiralis. We conclude that F. cottonii is not a coherent genetic entity, but an artificial grouping of evolutionarily independent populations that converged into similar morphologies in different salt-marsh habitats.

A microsatellite library was developed using genomic DNA of the Parsley frog, Pelodytes punctatus, an amphibian species which inhabits Mediterranean temporary pond systems. Number of alleles and heterozygosity ranged from 10 to 25 and from 0.66 to 0.90, respectively. Crossspecies amplification was successful for 13 of the 15 developed loci for the related species, Pelodytes ibericus. The high levels of polymorphism revealed by these loci will be extremely useful for characterizing the population genetic diversity and structure and to estimate levels of dispersal and gene flow in the species P. punctatus and P. ibericus.

Dispersal and vicariance are the principal mechanisms responsible for the formation of biogeographic patterns, driven or maintained by the role of past and current barriers to dispersal. Southwest Portugal harbors a rich endemic fauna and flora where strongly differentiated taxa can be observed, suggesting ancient isolating mechanisms acted in this region. In this study, we used information from two partial mitochondrial sequences, combined with information from microsatellite loci and amplification success, to investigate biogeographic patterns of genetic divergence in populations of Pleurodeles waltl in Portugal. Our results demonstrate genetic differentiation at different time frames creating distinct populations in southwest Portugal, which might have arisen following isolation by a large river estuary and mountainous barriers. Habitat destruction associated with agricultural intensification raises conservation concerns over the unique biodiversity in this region.

Fourteen highly polymorphic microsatellite markers were developed and characterized for the sharp-ribbed salamander, Pleurodeles waltl. Isolating microsatellites with more than 12 single repeat type units was only successful for a tetranucleotide repeat (ATAG). Compared to microsatellite libraries constructed simultaneously for two anuran amphibian species, a greater number of primer pairs designed for P. waltl had to be discarded, due to consistent amplification problems. Low amplification success rate for P. waltl may be due to its larger genome size. Consequently, to avoid nonspecific binding and to increase amplification success, polymerase chain reaction programmes with touchdown cycles were used. For 14 microsatellite markers, amplification was successful and consistent with number of alleles and expected heterozygosity ranging from seven to 22 and from 0.79 to 0.94, respectively. All 14 microsatellite markers will be extremely useful for metapopulation studies of this unique amphibian species.

Species of the family Syngnathidae are increasingly being investigated for conservation purposes but also for mating system and genetic parentage studies. The availability of highly polymorphic markers will be of great importance to conduct these kinds of studies. This paper describes the development and characterization of 10 polymorphic microsatellite markers for Hippocampus hippocampus and the utility of nine markers which were developed for a closely related species Hippocampus guttulatus. The number of alleles per locus developed for H. hippocampus ranged from 14 to 30, with levels of heterozygosity between 0.90 and 0.95. Most of the markers were successfully cross-amplified in the sister species, giving clear and unambiguous peaks and maintaining high levels of polymorphism.