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CO2 Exposure (co2 + exposure)
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] Linking microbial activity and soil organic matter transformations in forest soils under elevated CO2GLOBAL CHANGE BIOLOGY, Issue 2 2005S. A. Billings Abstract Soil organic matter (SOM) dynamics ultimately govern the ability of soil to provide long-term C sequestration and the nutrients required for ecosystem productivity. Predicting belowground responses to elevated CO2 requires an integrated understanding of SOM transformations and the microbial activity that governs them. It remains unclear how the microorganisms upon which these transformations depend will function in an elevated CO2 world. This study examines SOM transformations and microbial metabolism in soils from the Duke Free Air Carbon Enrichment site in North Carolina, USA. We assessed microbial respiration and net nitrogen (N) mineralization in soils with and without elevated CO2 exposure during a 100-day incubation. We also traced the depleted C isotopic signature of the supplemental CO2 into SOM and the soils' phospholipid fatty acids (PLFA), which serve as biomarkers for living cells. Cumulative net N mineralization in elevated CO2 soils was 50% that in control soils after a 100-day incubation. Respiration was not altered with elevated CO2. C : N ratios of bulk SOM did not change with elevated CO2, but incubation data suggest that the C : N ratios of mineralized organic matter increased with elevated CO2. Values of SOM ,13C were depleted with elevated CO2 (,26.7±0.2 vs. ,30.2±0.3,), reflecting the depleted signature of the supplemental CO2. We compared ,13C of individual PLFA with the ,13C of SOM to discern incorporation of the depleted C isotopic signature into soil microbial groups in elevated CO2 plots. PLFA i15:0, a15:0, and 10Met18:0 reflected significant incorporation of recently produced photosynthate, suggesting that the bacterial groups defined by these biomarkers are active metabolizers in elevated CO2 soils. At least one of these groups (actinomycetes, 10Met18:0) specializes in metabolizing less labile substrates. Because control plots did not receive an equivalent 13C tracer, we cannot determine from these data whether this group of organisms was stimulated by elevated CO2 compared with these organisms in control soils. Stimulation of this group, if it occurred in the elevated CO2 plot, would be consistent with a decline in the availability of mineralizable organic matter with elevated CO2, which incubation data suggest may be the case in these soils. [source] Seasonal changes in the effects of elevated CO2 on rice at three levels of nitrogen supply: a free air CO2 enrichment (FACE) experimentGLOBAL CHANGE BIOLOGY, Issue 6 2003HAN-YONG KIM Abstract Over time, the stimulative effect of elevated CO2 on the photosynthesis of rice crops is likely to be reduced with increasing duration of CO2 exposure, but the resultant effects on crop productivity remain unclear. To investigate seasonal changes in the effect of elevated CO2 on the growth of rice (Oryza sativa L.) crops, a free air CO2 enrichment (FACE) experiment was conducted at Shizukuishi, Iwate, Japan in 1998,2000. The target CO2 concentration of the FACE plots was 200 µmol mol,1 above that of ambient. Three levels of nitrogen (N) were supplied: low (LN, 4 g N m,2), medium [MN, 8 (1998) and 9 (1999, 2000) g N m,2] and high N (HN, 12 and 15 g N m,2). For MN and HN but not for LN, elevated CO2 increased tiller number at panicle initiation (PI) but this positive response decreased with crop development. As a result, the response of green leaf area index (GLAI) to elevated CO2 greatly varied with development, showing positive responses during vegetative stages and negative responses after PI. Elevated CO2 decreased leaf N concentration over the season, except during early stage of development. For MN crops, total biomass increased with elevated CO2, but the response declined linearly with development, with average increases of 32, 28, 21, 15 and 12% at tillering, PI, anthesis, mid-ripening and grain maturity, respectively. This decline is likely to be due to decreases in the positive effects of elevated CO2 on canopy photosynthesis because of reductions in both GLAI and leaf N. Up to PI, LN-crops tended to have a lower response to elevated CO2 than MN- and HN-crops, though by final harvest the total biomass response was similar for all N levels. For MN- and HN-crops, the positive response of grain yield (ca. 15%) to elevated CO2 was slightly greater than the response of final total biomass while for LN-crops it was less. We conclude that most of the seasonal changes in crop response to elevated CO2 are directly or indirectly associated with N uptake. [source] Corticosteroids and the cardiovascular response to stress: a pilot study of the 35% CO2 challenge in Addison's diseaseCLINICAL ENDOCRINOLOGY, Issue 3 2006J. M. Kaye Summary Objective, Glucocorticoids play an essential role in the neuroendocrine response to stress, influencing both the hypothalamic,pituitary,adrenal (HPA) axis and the sympatho-adrenomedullary (SAM) axis at several levels. In this pilot study, a clinical model of primary adrenocortical failure (Addison's disease, AD) has been used to evaluate the role of circulating glucocorticoids in both the autonomic and psychological response to stress. Design and subjects, Five subjects with known AD underwent a randomized, double-blind, placebo-controlled investigation in which they received fixed glucocorticoid plus mineralocorticoid hormone replacement or placebo for 48 h prior to a 35% CO2 challenge. Measurement, Psychological responses immediately before and after CO2 exposure were assessed by questionnaire. Systolic blood pressure (SBP) and heart rate were measured automatically at 1-min intervals for 5 min before and 5 min after the CO2 exposure. Results, While on hormone replacement, all subjects had an identical response to CO2 to that recorded in normal volunteers (initial bradycardia, an increase in blood pressure and subjective feelings of anxiety). On no replacement, however, the bradycardia and anxiety responses were not significantly altered, but the pressor response was markedly attenuated (+15·6 ± 5 mmHg on replacement compared with +4·2 ± 3·3 mmHg off replacement; P = 0·043). Conclusions, These data provide further evidence that the CO2 -induced bradycardia is a direct , presumably parasympathetic , response to CO2 independent of the pressor effect, and that the pressor response itself is dependent on the presence of the circulating corticosteroid. [source] | ||||||||||