Molecular Markers, Natural History, and Evolution. 2nd edition
By I. Lovette. 2004
359 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/ec1abf893e0cf89e9013437c088c636c905804e8
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In Molecular Biology
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Citations in the corpus
- Perspective: conservation genetics enters the genomics era (2010, background): “…polymorphic DNA) assays (1990s), microsatellite analyses (1990s), DNA barcoding based on a mitochondrial gene (2000s), and several other molecular approaches for revealing genetic variation in particular proteins or classes of nucleic acids (see Hillis et al. 1996; Avise 2004; Freeland 2005).”
- The phylogeographic architecture of the fucoid seaweed Ascophyllum nodosum: an intertidal ‘marine tree’ and survivor of more than one glacial–interglacial cycle (2010, background): “Discrepancies between mitochondrial and nuclear markers are typically associated with patterns of mitochondrial inheritance, sex skew or sex-biased dispersal (Avise, 2004).”
- Comparative phylogeography and species boundaries in Echinolittorina snails in the central Indo‐West Pacific (2006, background): “The discovery of spatial patterns that are congruent across taxonomic groups has always been emphasized as a powerful argument for the determination of phylogeographical structure by vicariant factors, whether these are eustatic, tectonic or climatic (Avise, 2000, 2004).”
- DNA Barcoding: Promise and Pitfalls (2004, neutral): “Given the long history of use of molecular markers (e.g., allozymes, rDNA, and mtDNA) for these purposes (Avise 2004), there is nothing fundamentally new in the DNA barcoding concept, except increased scale and proposed standardization.”
- Historical biogeography of two alpine butterflies in the Rocky Mountains: broad‐scale concordance and local‐scale discordance (2005, methodology): “The degree of genetic divergence, or isolation, at different geographic scales was assessed using FST, as is commonly done in studies of population structure (Avise, 2004).”
- Riverine and marine ecotypes of Sotalia dolphins are different species (2005, background): “Molecular data have proved to be useful sources of information on species boundaries (Knowlton 2000; Avise 2004).”
- DNA Barcoding is not enough: mismatch of taxonomy and genealogy in New Zealand grasshoppers (Orthoptera: Acrididae). (2008, background): “There is no doubt that mtDNA haplotype data have provided a powerful means to explore evolutionary history (genealogy) of species, informing on a wide range of evolutionary and ecological issues and revealing hitherto unrecognized (cryptic) diversity (Avise, 2004).”
- Genetic evaluation of marine biogeographical barriers: perspectives from two widespread Indo‐Pacific snappers (Lutjanus kasmira and Lutjanus fulvus) (2009, background): “These differences may result from the fourfold lower effective population size of the mitochondrial genome (Avise, 2004), although other factors such as differing mutation rates probably contribute as well.”
- Phylogeography of the pool frog Rana (Pelophylax) lessonae in the Italian peninsula and Sicily: multiple refugia, glacial expansions and nuclear–mitochondrial discordance (2008, background): “First, and most convincingly, it appears highly unparsimonious on the basis that it would imply that the independent signals at seven unlinked nuclear loci are less representative of the population history than is that of the single mtDNA genome (Funk & Omland, 2003; Avise, 2004; Ballard & Whitlock,”