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151. Correlates of hyperdiversity in southern African ice plants (Aizoaceae).

152. Genome size expansion and the relationship between nuclear DNA content and spore size in the Asplenium monanthes fern complex (Aspleniaceae).

153. Next-generation museomics disentangles one of the largest primate radiations.

154. Convergent evolution of floral signals underlies the success of Neotropical orchids.

155. Do global diversity patterns of vertebrates reflect those of monocots?

156. Aquaporin expression and function in human pluripotent stem cell-derived retinal pigmented epithelial cells.

157. Impedance spectra of polypyrrole coated platinum electrodes.

158. An extreme case of plant-insect codiversification: figs and fig-pollinating wasps.

159. Apomixis and reticulate evolution in the Asplenium monanthes fern complex.

160. Phylogenies reveal predictive power of traditional medicine in bioprospecting.

161. Arthrosis of glenohumeral joint after arthroscopic Bankart repair: a long-term follow-up of 13 years.

162. Electric impedance of human embryonic stem cell-derived retinal pigment epithelium.

163. Temporal patterns of nucleotide misincorporations and DNA fragmentation in ancient DNA.

164. Phylogenetic relationships among arecoid palms (Arecaceae: Arecoideae).

165. Speciation with gene flow on Lord Howe Island.

166. Cross-cultural comparison of three medicinal floras and implications for bioprospecting strategies.

167. Genomic profiling of plastid DNA variation in the Mediterranean olive tree.

168. Causes of plant diversification in the Cape biodiversity hotspot of South Africa.

169. Extinction risk and diversification are linked in a plant biodiversity hotspot.

170. Testing Darwin's naturalization hypothesis in the Azores.

171. Consistent phenological shifts in the making of a biodiversity hotspot: the Cape flora.

172. The effects of above- and belowground mutualisms on orchid speciation and coexistence.

173. The use of phylogeny to interpret cross-cultural patterns in plant use and guide medicinal plant discovery: an example from Pterocarpus (Leguminosae).

174. FReD: the floral reflectance database--a web portal for analyses of flower colour.

175. Evidence of recent and continuous speciation in a biodiversity hotspot: a population genetic approach in southern African gladioli (Gladiolus; Iridaceae).

176. Pollinator behaviour and plant speciation: can assortative mating and disruptive selection maintain distinct floral morphs in sympatry?

177. Unparalleled rates of species diversification in Europe.

178. Development of a complex floral trait: The pollinator-attracting petal spots of the beetle daisy, Gorteria diffusa (Asteraceae).

179. How sympatric is speciation in the Howea palms of Lord Howe Island?

180. Using fossils and molecular data to reveal the origins of the Cape proteas (subfamily Proteoideae).

181. Origin and diversification of the Greater Cape flora: ancient species repository, hot-bed of recent radiation, or both?

182. Complete generic-level phylogenetic analyses of palms (Arecaceae) with comparisons of supertree and supermatrix approaches.

183. Dissecting the plant-insect diversity relationship in the Cape.

184. Pollinators underestimated: a molecular phylogeny reveals widespread floral convergence in oil-secreting orchids (sub-tribe Coryciinae) of the Cape of South Africa.

186. Contrasted patterns of hyperdiversification in Mediterranean hotspots.

187. Phylogeny, biogeography, and ecology of Ficus section Malvanthera (Moraceae).

188. Large multi-gene phylogenetic trees of the grasses (Poaceae): progress towards complete tribal and generic level sampling.

189. DNA barcoding the floras of biodiversity hotspots.

190. Oligocene CO2 decline promoted C4 photosynthesis in grasses.

191. C4 Photosynthesis evolved in grasses via parallel adaptive genetic changes.

192. A rapid diversification of rainforest trees (Guatteria; Annonaceae) following dispersal from Central into South America.

193. The geographical pattern of speciation and floral diversification in the neotropics: the tribe sinningieae (gesneriaceae) as a case study.

194. Biogeographical and phylogenetic origins of African fig species (Ficus section Galoglychia).

195. Preserving the evolutionary potential of floras in biodiversity hotspots.

196. Evolutionary biology: genetics and bisexuality.

197. The mahogany family "out-of-Africa": divergence time estimation, global biogeographic patterns inferred from plastid rbcL DNA sequences, extant, and fossil distribution of diversity.

198. Sympatric speciation in palms on an oceanic island.

199. Neutral theory, phylogenies, and the relationship between phenotypic change and evolutionary rates.

200. 60 million years of co-divergence in the fig-wasp symbiosis.

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