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Selected AbstractsWide-area estimates of saltcedar (Tamarix spp.) evapotranspiration on the lower Colorado River measured by heat balance and remote sensing methods,,ECOHYDROLOGY, Issue 1 2009Pamela L. Nagler Abstract In many places along the lower Colorado River, saltcedar (Tamarix spp) has replaced the native shrubs and trees, including arrowweed, mesquite, cottonwood and willows. Some have advocated that by removing saltcedar, we could save water and create environments more favourable to these native species. To test these assumptions we compared sap flux measurements of water used by native species in contrast to saltcedar, and compared soil salinity, ground water depth and soil moisture across a gradient of 200,1500 m from the river's edge on a floodplain terrace at Cibola National Wildlife Refuge (CNWR). We found that the fraction of land covered (fc) with vegetation in 2005,2007 was similar to that occupied by native vegetation in 1938 using satellite-derived estimates and reprocessed aerial photographs scaled to comparable spatial resolutions (3,4 m). We converted fc to estimates of leaf area index (LAI) through point sampling and destructive analyses (r2 = 0·82). Saltcedar LAI averaged 2·54 with an fc of 0·80, and reached a maximum of 3·7 with an fc of 0·95. The ranges in fc and LAI are similar to those reported for native vegetation elsewhere and from the 1938 photographs over the study site. On-site measurements of water use and soil and aquifer properties confirmed that although saltcedar grows in areas where salinity has increased much better than native shrubs and trees, rates of transpiration are similar. Annual water use over CNWR was about 1·15 m year,1. Copyright © 2008 John Wiley & Sons, Ltd. [source] Could the tree diversity pattern in Europe be generated by postglacial dispersal limitation?ECOLOGY LETTERS, Issue 6 2007Jens-Christian Svenning Abstract The relative importance of contemporary climate and history as controls of geographical diversity patterns is intensely debated. A key example is the controversy over the extent to which temperate tree distributions and diversity patterns reflect postglacial dispersal limitation. Here, we focus on Central and Northern Europe, and show that recent estimates of tree migration rates < 100 m year,1 imply that many species have probably not reached equilibrium with climate in this region. We then demonstrate that geographical accessibility from glacial refuges explains 78% of the geographical variation in the region's tree diversity and is a much stronger diversity predictor than climate. Finally, we show that realistic estimates of migration rates can be derived from the observed tree diversity pattern by assuming it to be purely dispersal driven. In conclusion, the tree diversity pattern in Central and Northern Europe could, to a large extent, be a result of postglacial dispersal limitation. [source] Isotopic and petrological evidence of fluid,rock interaction at a Tethyan ocean,continent transition in the Alps: implications for tectonic processes and carbon transfer during early ocean formationGEOFLUIDS (ELECTRONIC), Issue 4 2007A. ENGSTRÖM Abstract We report overprinting stable isotope evidence of fluid,rock interaction below two detachment faults along which mantle rocks were exhumed to the seafloor, between the respective landward and seaward limits of oceanic and continental crust, at a Tethyan ocean,continent transition (OCT). This OCT, which is presently exposed in the Tasna nappe (south-eastern Switzerland) is considered an on-land analogue of the well-studied Iberian OCT. We compare our results with the fault architecture (fault core,damage zone,protolith) described by Caine et al. [Geology (1996) Vol. 24, pp. 1025,1028]. We confirm the existence of a sharp boundary between the fault core and damage zone based on isotopic data, but the boundary between the damage zone and protolith is gradational. We identify evidence for: (1) pervasive isotopic modification to 8.4 ± 0.1, which accompanied or post-dated serpentinization of these mantle rocks at an estimated temperature of 67,109°C, (2) either (i) partial isolation of some highly strained regions [fault core(s) and mylonite] from this pervasive isotopic modification, because of permeability reduction (Caine et al.) or (ii) subsequent isotopic modification caused by structurally channelled flow of warm fluids within these highly strained regions, because of permeability enhancement, and (3) isotopic modification, which is associated with extensive calcification at T = 54,100°C, primarily beneath the younger of the two detachment faults and post-dating initial serpentinization. By comparing the volumetric extent of calcification with an experimentally verified model for calcite precipitation in veins, we conclude that calcification could have occurred in response to seawater infiltration, with a calculated flux rate of 0.1,0.2 m year,1 and a minimum duration of 0.2,4.0 × 104 years. The associated time-averaged uptake flux of carbon during this period was 8,120 mol m,2 year,1. By comparison with the estimated area of exhumed mantle rocks at the Iberian OCT, we calculate a maximum annual uptake flux for carbon of 2,30 Tg year,1. This is an order of magnitude greater than that for carbon exchange at the mid-ocean ridges and 0.1,1.4% of the global oceanic uptake flux for carbon. [source] Forest progression modes in littoral Congo, Central Atlantic AfricaJOURNAL OF BIOGEOGRAPHY, Issue 9 2004Charly Favier Abstract Aim, To understand the persistence of a forest,savanna mosaic in places where rainfall data suggest that forest take-over should take place. To study the various modes of forest encroachment, and the role of human activities to hamper it. Location, Data were collected on several forest,savanna ecotones in the coastal region of the Republic of Congo. The sites were chosen to illustrate the differing principal modes of forest expansion, corresponding to different levels of anthropic pressure. Methods, The study sites were situated on five transects perpendicular to the ecotone (total sampled area: 1.7 ha) and 10 forest clumps in savanna (with diameters from 3 to 20 m). Along the transects botanical identification, diameter measurement and cartography were performed, while leaf area index was measured at a high resolution (every metre) along two of them. Collected data were analysed using a continuous quantification approach, which is much more useful than classical quadrat analysis. Time calibration of progression rates was performed using a simple model of the growth of the characteristic pioneer species, Aucoumea klaineana. Results, The two main different modes are reflected in different successional patterns. The edge diffusion is slow (its rate is evaluated to c. 1 m year,1) and is characterized by a progressive increase in large-diameter tree density and shade-tolerant tree density away from the ecotone. Conversely, savanna to forest phase transition by coalescence of clumps exhibits high tree density remnants distributed in established forest. The composition of these remnants is compatible with that of the forest clumps in savannas. Main conclusions, Three functional groups of pioneer trees are distinguished: some occupy the edge (edge pioneer), others establish clumps of forest in savanna (clump pioneers) and the longer-living A. klaineana ensures the transition to ,mature' forest. The two different observed patterns (linear edge progression and clump coalescence) can be understood with the use of a model of forest,savanna dynamics, ,FORSAT'. The two control parameters are the annual rainfall and the frequency of man-made fires in each savanna. In particular, an increase in the fire frequency can lead to a shift from the coalescence regime to the edge progression one. [source] Estimated migration rates under scenarios of global climate changeJOURNAL OF BIOGEOGRAPHY, Issue 7 2002Jay R. Malcolm Aim Greenhouse-induced warming and resulting shifts in climatic zones may exceed the migration capabilities of some species. We used fourteen combinations of General Circulation Models (GCMs) and Global Vegetation Models (GVMs) to investigate possible migration rates required under CO2 -doubled climatic forcing. Location Global. Methods Migration distances were calculated between grid cells of future biome type x and nearest same-biome-type cells in the current climate. In `base-case' calculations, we assumed that 2 × CO2 climate forcing would occur in 100 years, we used ten biome types and we measured migration distances as straight-line distances ignoring water barriers and human development. In sensitivity analyses, we investigated different time periods of 2 × CO2 climate forcing, more narrowly defined biomes and barriers because of water bodies and human development. Results In the base-case calculations, average migration rates varied significantly according to the GVM used (BIOME3 vs. MAPSS), the age of the GCM (older- vs. newer-generation GCMs), and whether or not GCMs included sulphate cooling or CO2 fertilization effects. However, high migration rates (, 1000 m year,1) were relatively common in all models, consisting on average of 17% grid cells for BIOME3 and 21% for MAPSS. Migration rates were much higher in boreal and temperate biomes than in tropical biomes. Doubling of the time period of 2 × CO2 forcing reduced these areas of high migration rates to c. 12% of grid cells for both BIOME3 and MAPSS. However, to obtain migration rates in the Boreal biome that were similar in magnitude to those observed for spruce when it followed the retreating North American Glacier, a radical increase in the period of warming was required, from 100 to >1000 years. A reduction in biome area by an order of magnitude increased migration rates by one to three orders of magnitude, depending on the GVM. Large water bodies and human development had regionally important effects in increasing migration rates. Main conclusions In conclusion, evidence from coupled GCMs and GVMs suggests that global warming may require migration rates much faster than those observed during post-glacial times and hence has the potential to reduce biodiversity by selecting for highly mobile and opportunistic species. Several poorly understood factors that are expected to influence the magnitude of any such reduction are discussed, including intrinsic migrational capabilities, barriers to migration, the role of outlier populations in increasing migration rates, the role of climate in setting range limits and variation in species range sizes. [source] | ||||||||||