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C4 Grasslands (c4 + grassland)
Selected AbstractsC3,C4 composition and prior carbon dioxide treatment regulate the response of grassland carbon and water fluxes to carbon dioxideFUNCTIONAL ECOLOGY, Issue 1 2007H. W. POLLEY Summary 1Plants usually respond to carbon dioxide (CO2) enrichment by increasing photosynthesis and reducing transpiration, but these initial responses to CO2 may not be sustained. 2During May, July and October 2000, we measured the effects of temporarily increasing or decreasing CO2 concentration by 150,200 µmol mol,1 on daytime net ecosystem CO2 exchange (NEE) and water flux (evapotranspiration, ET) of C3,C4 grassland in central Texas, USA that had been exposed for three growing seasons to a CO2 gradient from 200 to 560 µmol mol,1. Grassland grown at subambient CO2 (< 365 µmol mol,1) was exposed for 2 days to an elevated CO2 gradient (> 365 µmol mol,1). Grassland grown at elevated CO2 was exposed for 2 days to a subambient gradient. Our objective was to determine whether growth CO2 affected the amount by which grassland NEE and ET responded to CO2 switching (sensitivity to CO2). 3The NEE per unit of leaf area was greater (16,20%) and ET was smaller (9,20%), on average, at the higher CO2 concentration during CO2 switching in May and July. The amount by which NEE increased at the higher CO2 level was smaller at elevated than subambient growth concentrations on both dates, but relationships between NEE response and growth CO2 were weak. Conversely, the effect of temporary CO2 change on ET did not depend on growth CO2. 4The ratio of NEE at high CO2 to NEE at low CO2 during CO2 change in July increased from 1·0 to 1·26 as the contribution of C3 cover to total cover increased from 26% to 96%. Conversely, in May, temporary CO2 enrichment reduced ET more in C4 - than C3 -dominated grassland. 5For this mesic grassland, sensitivity of NEE and ET to brief change in CO2 depended as much on the C3,C4 composition of vegetation as on physiological adjustments related to prior CO2 exposure. [source] Carbon sequestration in arid-land forestGLOBAL CHANGE BIOLOGY, Issue 5 2003J. M. GRÜNZWEIG Abstract Rising atmospheric CO2 concentrations may lead to increased water availability because the water use efficiency of photosynthesis (WUE) increases with CO2 in most plant species. This should allow the extension of afforestation activities into drier regions. Using eddy flux, physiological and inventory measurements we provide the first quantitative information on such potential from a 35-year old afforestation system of Aleppo pine (Pinus halepensis Mill.) at the edge of the Negev desert. This 2800 ha arid-land forest contains 6.5 ± 1.2 kg C m,2, and continues to accumulate 0.13,0.24 kg C m,2 yr,1. The CO2 uptake is highest during the winter, out of phase with most northern hemispheric forest activity. This seasonal offset offers low latitude forests ,10 ppm higher CO2 concentrations than that available to higher latitude forests during the productive season, in addition to the 30% increase in mean atmospheric CO2 concentrations since the 1850s. Expanding afforestation efforts into drier regions may be significant for C sequestration and associated benefits (restoration of degraded land, reducing runoff, erosion and soil compaction, improving wildlife) because of the large spatial scale of the regions potentially involved (ca. 2 × 109 ha of global shrub-land and C4 grassland). Quantitative information on forest activities under dry conditions may also become relevant to regions predicted to undergo increasing aridity. [source] Fire and the Miocene expansion of C4 grasslandsECOLOGY LETTERS, Issue 7 2005Jon E. Keeley Abstract C4 photosynthesis had a mid-Tertiary origin that was tied to declining atmospheric CO2, but C4 -dominated grasslands did not appear until late Tertiary. According to the ,CO2 -threshold' model, these C4 grasslands owe their origin to a further late Miocene decline in CO2 that gave C4 grasses a photosynthetic advantage. This model is most appropriate for explaining replacement of C3 grasslands by C4 grasslands, however, fossil evidence shows C4 grasslands replaced woodlands. An additional weakness in the threshold model is that recent estimates do not support a late Miocene drop in pCO2. We hypothesize that late Miocene climate changes created a fire climate capable of replacing woodlands with C4 grasslands. Critical elements were seasonality that sustained high biomass production part of year, followed by a dry season that greatly reduced fuel moisture, coupled with a monsoon climate that generated abundant lightning-igniting fires. As woodlands became more open from burning, the high light conditions favoured C4 grasses over C3 grasses, and in a feedback process, the elevated productivity of C4 grasses increased highly combustible fuel loads that further increased fire activity. This hypothesis is supported by paleosol data that indicate the late Miocene expansion of C4 grasslands was the result of grassland expansion into more mesic environments and by charcoal sediment profiles that parallel the late Miocene expansion of C4 grasslands. Many contemporary C4 grasslands are fire dependent and are invaded by woodlands upon cessation of burning. Thus, we maintain that the factors driving the late Miocene expansion of C4 were the same as those responsible for maintenance of C4 grasslands today. [source] The antiquity of Madagascar's grasslands and the rise of C4 grassy biomesJOURNAL OF BIOGEOGRAPHY, Issue 10 2008William J. Bond Abstract Aim, Grasslands and savannas, which make up > 75% of Madagascar's land area, have long been viewed as anthropogenically derived after people settled on the island c. 2 ka. We investigated this hypothesis and an alternative , that the grasslands are an insular example of the post-Miocene spread of C4 grassy biomes world-wide. Location, Madagascar, southern Africa, East Africa. Methods, We compared the number of C4 grass genera in Madagascar with that in southern and south-central African floras. If the grasslands are recent we would expect to find fewer species and genera in Madagascar relative to Africa and for these species and genera to have very wide distribution ranges in Madagascar. Secondly, we searched Madagascan floras for the presence of endemic plant species or genera restricted to grasslands. We also searched for evidence of a grassland specialist fauna with species endemic to Madagascar. Plant and animal species endemic to C4 grassy biomes would not be expected if these are of recent origin. Results, Madagascar has c. 88 C4 grass genera, including six endemic genera. Excluding African genera with only one or two species, Madagascar has 86.6% of southern Africa's and 89.4% of south-central Africa's grass genera. C4 grass species make up c. 4% of the flora of both Madagascar and southern Africa and species : genus ratios are similar (4.3 and 5.1, respectively). Turnover of grasses along geographical gradients follows similar patterns to those in South Africa, with Andropogoneae dominating in mesic biomes and Chlorideae in semi-arid grassy biomes. At least 16 monocot genera have grassland members, many of which are endemic to Madagascar. Woody species in frequently burnt savannas include both Madagascan endemics and African species. A different woody flora, mostly endemic, occurs in less frequently burnt grasslands in the central highlands, filling a similar successional niche to montane C4 grasslands in Africa. Diverse vertebrate and invertebrate lineages have grassland specialists, including many endemic to Madagascar (e.g. termites, ants, lizards, snakes, birds and mammals). Grassland use of the extinct fauna is poorly known but carbon isotope analysis indicates that a hippo, two giant tortoises and one extinct lemur ate C4 or CAM (crassulacean acid metabolism) plants. Main conclusions, The diversity of C4 grass lineages in Madagascar relative to that in Africa, and the presence of plant and animal species endemic to Madagascan grassy biomes, does not fit the view that these grasslands are anthropogenically derived. We suggest that grasslands invaded Madagascar after the late Miocene, part of the world-wide expansion of C4 grassy biomes. Madagascar provides an interesting test case for biogeographical analysis of how these novel biomes assembled, and the sources of the flora and fauna that now occupy them. A necessary part of such an analysis would be to establish the pre-settlement extent of the C4 grassy biomes. Carbon isotope analysis of soil organic matter would be a feasible method for doing this. [source] | ||||||||||