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202. Bacterial Infections in Travellers.

203. Relationship between corrected TIMI frame counts at three weeks and late survival after myocardial infarction

204. Public Sector Capital and the Transition from Dictatorship to Democracy.

213. Abnormal Coronary Flow in Infarct Arteries 1 Year After Myocardial Infarction Is Predicted at 4 Weeks by Corrected Thrombolysis in Myocardial Infarction (TIMI) Frame Count and Stenosis Severity 11This work was supported in part by a grant from the Health Research Council of New Zealand, Auckland, New Zealand.

220. Signatures of autogenic epiphyte succession for an aspen chronosequence.

221. A risk-based model of climate change threat: hazard, exposure, and vulnerability in the ecology of lichen epiphytes.

222. The Psychological Impact of Test Results Following Diagnostic Coronary CT Angiography.

224. Local experimental growth rates respond to macroclimate for the lichen epiphyte Lobaria pulmonaria.

225. Archaeobotanical evidence for a massive loss of epiphyte species richness during industrialization in southern England.

226. The Younger Dryas and Late Pleistocene peoples of the Great Lakes region

227. DNA barcoding of lichenized fungi demonstrates high identification success in a floristic context.

228. Information Cascades and Revolutionary Regime Transitions.

229. New Antiplatelet Strategies in the Adjunctive Treatment of Acute Myocardial Infarction.

230. Epiphyte sensitivity to a cross-scale interaction between habitat quality and macroclimate: an opportunity for range-edge conservation.

231. Species interaction and response to wind speed alter the impact of projected temperature change in a montane ecosystem.

232. Quantifying the role of deterministic assembly and stochastic drift in a natural community of Arctic mosses.

233. Integrating multiple landscape-scale drivers in the lichen epiphyte response: climatic setting, pollution regime and woodland spatial-temporal structure.

235. UNDERSTANDING CACHE VARIABILITY: A DELIBERATELY BURNED EARLY PALEOINDIAN TOOL ASSEMBLAGE FROM THE CROWFIELD SITE, SOUTHWESTERN ONTARIO, CANADA.

236. Local extent of old-growth woodland modifies epiphyte response to climate change.

237. Estimating nitrogen risk to Himalayan forests using thresholds for lichen bioindicators.

239. Paleoecological Evidence for Transitions between Contrasting Landforms in a Polygon-Patterned High Arctic Wetland.

240. Interactions between hydrology, burning and contrasting plant groups during the millennial-scale development of sub-montane wet heath.

241. Changing climate and historic-woodland structure interact to control species diversity of the 'Lobarion' epiphyte community in Scotland.

242. 19th century woodland structure controls stand-scale epiphyte diversity in present-day Scotland.

243. Contrasting functional traits maintain lichen epiphyte diversity in response to climate and autogenic succession.

244. Long-term sensitivity of a High Arctic wetland to Holocene climate change.

245. PRIVATIZATION AND STRATEGIC MONITORING WITH GAUSSIAN PRIORS.

246. Soil as a potential source of nitrogen for mat-forming lichens.

247. The natural abundance of 15N in mat-forming lichens.

248. Ecology of Racomitrium lanuginosum in British blanket mire--evidence from the palaeoecological record.

249. Blackwell Science Ltd Climatic control of peat erosion in a North Wales blanket mire.

250. EVIDENCE FOR LATE PALEOINDIAN RITUAL FROM THE CARADOC SITE (AfHj-104), SOUTHWESTERN ONTARIO, CANADA.

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