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248 results on '"Faircloth, Brant C."'

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201. Tetranucleotide,trinucleotide,and dinucleotide loci from the bobcat (Lynx rufus ).

202. Dispersal sweepstakes: Biotic interchange propelled air‐breathing fishes across the globe.

204. Comparison of ultraconserved elements (UCEs) to microsatellite markers for the study of avian hybrid zones: a test in Aphelocoma jays.

207. Earth history and the passerine superradiation

213. Widespread sympatry in a species-rich clade of marine fishes (Carangoidei).

214. Use of Sonic Tomography to Detect and Quantify Wood Decay in Living Trees

216. The evolution of peafowl and other taxa with ocelli (eyespots): a phylogenomic approach.

217. A reference genome for Bluegill (Centrarchidae: Lepomis macrochirus).

218. Ultraconserved elements are novel phylogenomic markers that resolve placental mammal phylogeny when combined with species-tree analysis.

219. Phylogenomics and biogeography of sawflies and woodwasps (Hymenoptera, Symphyta).

220. Biogeography of a neotropical songbird radiation reveals similar diversification dynamics between montane and lowland clades.

221. Displaced clines in an avian hybrid zone (Thamnophilidae: Rhegmatorhina) within an Amazonian interfluve*.

222. A phylogenomic framework for pelagiarian fishes (Acanthomorpha: Percomorpha) highlights mosaic radiation in the open ocean.

224. Allele Phasing Greatly Improves the Phylogenetic Utility of Ultraconserved Elements.

225. Dry habitats were crucibles of domestication in the evolution of agriculture in ants.

226. Genome-wide ultraconserved elements exhibit higher phylogenetic informativeness than traditional gene markers in percomorph fishes.

227. Historical specimens and the limits of subspecies phylogenomics in the New World quails (Odontophoridae).

228. Earth history and the passerine superradiation

229. The coevolution of fungus-ant agriculture.

230. Complexity of avian evolution revealed by family-level genomes.

231. An island 'endemic' born out of hybridization between introduced lineages.

232. Implications of headwater contact zones for the riverine barrier hypothesis: a case study of the Blue-capped Manakin (Lepidothrix coronata).

233. A high-quality de novo genome assembly for clapper rail (Rallus crepitans).

234. The AEGEAN-169 clade of bacterioplankton is synonymous with SAR11 subclade V (HIMB59) and metabolically distinct.

235. Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa.

236. Prolonged morphological expansion of spiny-rayed fishes following the end-Cretaceous.

237. Displaced clines in an avian hybrid zone (Thamnophilidae: Rhegmatorhina) within an Amazonian interfluve .

238. Dense sampling of bird diversity increases power of comparative genomics.

239. Palaeoclimate ocean conditions shaped the evolution of corals and their skeletons through deep time.

240. Adapterama II: universal amplicon sequencing on Illumina platforms (TaggiMatrix).

241. Earth history and the passerine superradiation.

242. Cultivation and genomics of the first freshwater SAR11 (LD12) isolate.

243. Explosive diversification of marine fishes at the Cretaceous-Palaeogene boundary.

244. Conflicting Evolutionary Histories of the Mitochondrial and Nuclear Genomes in New World Myotis Bats.

245. Phylogenomic Systematics of Ostariophysan Fishes: Ultraconserved Elements Support the Surprising Non-Monophyly of Characiformes.

246. Replicated divergence in cichlid radiations mirrors a major vertebrate innovation.

247. Three crocodilian genomes reveal ancestral patterns of evolution among archosaurs.

248. The evolution of peafowl and other taxa with ocelli (eyespots): a phylogenomic approach.

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