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1.
Atmospheric CO2 concentration is rising and it has been suggested that a portion of the additional carbon is being sequestered in terrestrial vegetation and much of that in below-ground structures. The objective of the present study was to quantify the effects of elevated atmospheric CO2 on fine root length and distribution with depth with minirhizotrons in an open-top chamber experiment in an oak-palmetto scrub ecosystem at Kennedy Space Centre, Florida, USA. Observations were made five times over a period of one and a half years in three ambient chambers (350 p.p.m. CO2), three CO2 enriched chambers (700 p.p.m. CO2), and three unchambered plots. Greater root length densities were produced in the elevated CO2 chambers (14.2 mm cm?2) compared to the ambient chambers (8.7 mm cm?2). More roots may presumably lead to more efficient acquisition of resources. Fine root abundance varied significantly with soil depth, and there appeared to be enhanced proliferation of fine roots near the surface (0–12 cm) and at greater depth (49–61 cm) in the elevated CO2 chambers. The vertical root distribution pattern may be a response to availability of nutrients and water. More studies are needed to determine if increased root length under CO2 enriched conditions actually results in greater sequestering of carbon below ground.  相似文献   

2.
Increased below-ground carbon allocation in forest ecosystems is a likely consequence of rising atmospheric CO2 concentration. If this results in changes to fine root growth, turnover and distribution long-term soil carbon cycling and storage could be altered. Bi-weekly measurements were made to determine the dynamics and distribution of fine roots (< 1 mm diameter) for Pinus radiata trees growing at ambient (350 μmol mol–1) and elevated (650 μmol mol–1) CO2 concentration in large open-top chambers. Measurements were made using minirhizotrons installed horizontally at depths of 0.1, 0.3, 0.5 and 0.9 m. During the first year, at a depth of 0.3 m, the increase in relative growth rate of roots occurred 6 weeks earlier in the elevated CO2 treatment and the maximum rate was reached 10 weeks earlier than for trees in the ambient treatment. After 2 years, cumulative fine root growth (Pt) was 36% greater for trees growing at elevated CO2 than at ambient CO2 concentration, although this difference was not significant. A model of root growth driven by daily soil temperature accounted for between 43 and 99% of root growth variability. Total root loss (Lt) was 9% in the ambient and 14% in the elevated CO2 treatment, although this difference was not significant. Root loss was greatest at 0.3 m. In the first year, 62% of fine roots grown between mid-summer and late-autumn disappeared within a year in the elevated CO2 treatment, but only 18% in the ambient CO2 treatment (P < 0.01). An exponential model relating Lt to time accounted for between 74 and 99% of the variability. Root cohort half-lives were 951 d for the ambient and 333 d for the elevated treatment. Root length density decreased exponentially with depth in both treatments, but relatively more fine roots grown in the elevated CO2 treatment tended to occur deeper in the soil profile.  相似文献   

3.
Scots pine (Pinus sylvestris L.) seedlings were grown for 3years in the ground in open top chambers and exposed to twoconcentrations of atmospheric CO2(ambient or ambient + 400 µmol mol-1) without addition of nutrients and water. Biomassproduction (above-ground and below-ground) and allocation, aswell as canopy structure and tissue nitrogen concentrationsand contents, were examined by destructive harvest after 3 years.Elevated CO2increased total biomass production by 55%, reducedneedle area and needle mass as indicated, respectively, by lowerleaf area ratio and leaf mass ratio. A relatively smaller totalneedle area was produced in relation to fine roots under elevatedCO2. The proportion of dry matter in roots was increased byelevated CO2, as indicated by increased root-to-shoot ratioand root mass ratio. Within the root system, there was a significantshift in the allocation towards fine roots. Root litter constituteda much higher fraction of fine roots in trees grown in the elevatedCO2than in those grown in ambient CO2. Growth at elevated CO2causeda significant decline in nitrogen concentration only in theneedles, while nitrogen content significantly increased in branchesand fine roots (with diameter less than 1 mm). There were nochanges in crown structure (branch number and needle area distribution).Based upon measurements of growth made throughout the 3 years,the greatest increase in biomass under elevated CO2took placemainly at the beginning of the experiment, when trees grownin elevated CO2had higher relative growth rates than those grownunder ambient CO2; these differences disappeared with time.Symptoms of acclimation of trees to growth in the elevated CO2treatmentwere observed and are discussed. Copyright 2000 Annals of BotanyCompany Elevated CO2, Pinus sylvestris, biomass production, allocation, fine roots, root litter, crown structure, nitrogen, C/N ratio  相似文献   

4.
Young Scots pine trees naturally established at a pine heath were exposed to two concentrations of CO2 (ambient and doubled ambient) and two O3 regimes (ambient and doubled ambient) and their combination in open-top field chambers during growing seasons 1994, 1995 and 1996 (late May to 15 September). Filtered ozone treatment and chamberless control trees were also included in the treatment comparisons. Root ingrowth cores were inserted to the undisturbed soil below the branch projection of each tree at the beginning of the fumigation period in 1994 and were harvested at the end of the fumigation periods in 1995 and 1996. Root biomasses were determined from different soil layers in the ingrowth cores, and the infection levels of different mycorrhizal types were calculated. Elevated O3 and CO2 did not have significant effects on the biomass production of Scots pine coarse (Ø > 2 mm) or fine roots (Ø < 2 mm) and roots of grasses and dwarf shrubs. Elevated O3 caused a transient stimulation, observable in 1995, in the proportion of tuber-like mycorrhizas, total mycorrhizas and total short roots but this stimulation disappeared during the last study year. Elevated CO2 did not enhance carbon allocation to root growth or mycorrhiza formation, although a diminishing trend in the mycorrhiza formation was observed. In the combination treatment increased CO2 inhibited the transient stimulating effect of ozone, and a significant increase of old mycorrhizas was observed. Our conclusion is that doubled CO2 is not able to increase carbon allocation to growth of fine roots or mycorrhizas in nutrient poor forest sites and realistically elevated ozone does not cause a measurable limitation to roots within a period of three exposure years.  相似文献   

5.
In this study, we investigated the impact of elevated atmospheric CO2 (ambient + 350 μmol mol–1) on fine root production and respiration in Scots pine (Pinus sylvestris L.) seedlings. After six months exposure to elevated CO2, root production measured by root in-growth bags, showed significant increases in mean total root length and biomass, which were more than 100% greater compared to the ambient treatment. This increased root length may have lead to a more intensive soil exploration. Chemical analysis of the roots showed that the roots in the elevated treatment accumulated more starch and had a lower C/N-ratio. Specific root respiration rates were significantly higher in the elevated treatment and this was probably attributed to increased nitrogen concentrations in the roots. Rhizospheric respiration and soil CO2 efflux were also enhanced in the elevated treatment. These results clearly indicate that under elevated atmospheric CO2 root production and development in Scots pine seedlings is altered and respiratory carbon losses through the root system are increased.  相似文献   

6.
Elevated atmospheric carbon dioxide (CO2) often stimulates the growth of fine roots, yet there are few reports of responses of intact root systems to long‐term CO2 exposure. We investigated the effects of elevated CO2 on fine root growth using open top chambers in a scrub oak ecosystem at Kennedy Space Center, Florida for more than 7 years. CO2 enrichment began immediately after a controlled burn, which simulated the natural disturbance that occurs in this system every 10–15 years. We hypothesized that (1) root abundance would increase in both treatments as the system recovered from fire; (2) elevated CO2 would stimulate root growth; and (3) elevated CO2 would alter root distribution. Minirhizotron tubes were used to measure fine root length density (mm cm?2) every three months. During the first 2 years after fire recovery, fine root abundance increased in all treatments and elevated CO2 significantly enhanced root abundance, causing a maximum stimulation of 181% after 20 months. The CO2 stimulation was initially more pronounced in the top 10 cm and 38–49 cm below the soil surface. However, these responses completely disappeared during the third year of experimental treatment: elevated CO2 had no effect on root abundance or on the depth distribution of fine roots during years 3–7. The results suggest that, within a few years following fire, fine roots in this scrub oak ecosystem reach closure, defined here as a dynamic equilibrium between production and mortality. These results further suggest that elevated CO2 hastens root closure but does not affect maximum root abundance. Limitation of fine root growth by belowground resources – particularly nutrients in this nutrient‐poor soil – may explain the transient response to elevated CO2.  相似文献   

7.
Mass loss, together with nitrogen and carbon loss, from above-ground material and roots of Festuca vivipara were followed for 13 months in a high Arctic polar semi-desert and a low Arctic tree-line dwarf shrub heath. Festuca vivipara for the study was obtained from plants cultivated at two different CO2 concentrations (350 and 500 μL L–1) in controlled environment chambers in the UK. Each of the four resource types (shoots or roots from plants grown in elevated or ambient CO2 concentrations) was subsequently placed in an experiment simulating aspects of environmental change in each Arctic ecosystem. Air, litter and soil temperatures were increased using open-topped polythene tents at both sites, and a 58% increase in summer precipitation was simulated at the high Arctic site. Mass loss was greatest at the low Arctic site, and from the shoot material, rather than the roots. Shoots grown under an elevated CO2 concentration decomposed more slowly at the high Arctic site, and more quickly at the low Arctic one, than shoots grown at ambient CO2. After 13 months, greater amounts of C and N remained in above-ground litter from plants grown under elevated, rather than ambient, CO2 at the polar semi-desert site, although lower amounts of C remained in elevated CO2 litter at the low Arctic ecosystem. In the high Arctic, roots grown in the 500 μL L–1 CO2 concentration decomposed significantly more slowly than below-ground material derived from the ambient CO2 chambers. Elevated CO2 concentrations significantly increased the inital C:N ratio, % soluble carbohydrates and α-cellulose content, and significantly decreased the inital N content, of the above-ground material compared to that derived from the ambient treatment. Initially, the C:N ratio and percentage N were similar in both sets of roots derived from the two different CO2 treatments, but soluble carbohydrate and α-cellulose concentrations were higher, and percentage lignin lower, in the elevated CO2 treatments.The tent treatments significantly retarded shoot decomposition in both ecosystems, probably because of lower litter bag moisture contents, although the additional precipitation treatment had no effect on mass loss from the above-ground material. The results suggest that neither additional summer precipitation (up to 58%), nor soil temperature increase of 1 °C, which may occur by the end of the next century as an effect of a predicted 4 °C rise in air temperature, had an appreciable effect on root decomposition in the short term in a high Arctic soil. However, at the low Arctic site, greater root decomposition, and a lower pool of root N remaining, were observed where soil temperature was increased by 2 °C in response to a 4 °C rise in air temperature. These results suggest that decomposition below-ground in this ecosystem would increase as an effect of predicted climate change. These data also show that there is a difference in the initial results of decomposition processes between the two Arctic ecosystems in response to simulated environmental change.  相似文献   

8.
 Carbon dioxide enrichment may increase the Al tolerance of trees by increasing root growth, root exudation and/or mycorrhizal colonization. The effect of elevated CO2 on the response of mycorrhizal pitch pine (Pinus rigida Mill.) seedlings to Al was determined in two experiments with different levels of nutrients, 0.1- or 0.2-strength Clark solution. During each experiment, seedlings inoculated with the ectomycorrhizal fungus Pisolithus tinctorius (Pers.) Coker & Couch were grown 13 weeks in sand irrigated with nutrient solution (pH 3.8) containing 0, 6.25, 12.5, or 25 mg/l Al (0, 232, 463, or 927 μM Al) in growth chambers fumigated with 350 (ambient) or 700 (elevated) μl/l CO2. At ambient CO2, in the absence of Al, mean total dry weights (DW) of seedlings at the high nutrient level were 164% higher than those at the low level. Total DW at elevated CO2, in the absence of Al, was significantly greater than that in ambient CO2 at the low (+34%) and high (+16%) nutrient levels. Root and shoot DW at both nutrient levels decreased with increasing Al concentrations with Al reducing root growth more than shoot growth. Although visible symptoms of Al toxicity in roots and needles were reduced by CO2 enrichment, there were no significant CO2 × Al interactions for shoot or root DW. The percentage of seedling roots that became mycorrhizal was negatively related to nutrient level and was greater at elevated than at ambient CO2 levels. Generally, elevated CO2 had little effect on concentration of mineral nutrients in roots and needles. Aluminum reduced concentrations of most nutrients by inhibiting uptake. Received: 18 June 1997 / Accepted: 8 December 1997  相似文献   

9.
The effects of CO2 elevation on the dynamics of fine root (FR) mass and ectomycorrhizal (EM) mass and colonization were studied in situ in a Florida scrub oak system over four years of postfire regeneration. Soil cores were taken at five dates and sorted to assess the standing crop of ectomycorrhizal and fine roots. We used ingrowth bags to estimate the effects of elevated CO2 on production of EM roots and fine roots. Elevated CO2 tended to increase EM colonization frequency but did not affect EM mass nor FR mass in soil cores (standing mass). However, elevated CO2 strongly increased EM mass and FR mass in ingrowth bags (production), but it did not affect the EM colonization frequency therein. An increase in belowground production with unchanged biomass indicates that elevated CO2 may stimulate root turnover. The CO2-stimulated increase of belowground production was initially larger than that of aboveground production. The oaks may allocate a larger portion of resources to root/mycorrhizal production in this system in elevated rather than ambient CO2.  相似文献   

10.
To determine the long-term impact of elevated CO2 on primary production of native tallgrass prairie, we compared the responses of tallgrass prairie at ambient and twice-ambient atmospheric CO2 levels over an 8-year period. Plots in open-top chambers (4.5 m diameter) were exposed continuously (24 h) to ambient and elevated CO2 from early April to late October each year. Unchambered plots were monitored also. Above-ground peak biomass was determined by clipping each year in early August, and root growth was estimated by harvesting roots from root ingrowth bags. Plant community composition was censused each year in early June. In the last 2 years of the study, subplots were clipped on 1 June or 1 July, and regrowth was harvested on 1 October. Volumetric soil water content of the 0–100 cm soil layer was determined using neutron scattering, and was generally higher in elevated CO2 plots than ambient. Peak above-ground biomass was greater on elevated CO2 plots than ambient CO2 plots with or without chambers during years with significant plant water stress. Above-ground regrowth biomass was greater under elevated CO2 than under ambient CO2 in a year with late-season water stress, but did not differ in a wetter year. Root ingrowth biomass was also greater in elevated CO2 plots than ambient CO2 plots when water stress occurred during the growing season. The basal cover and relative amount of warm-season perennial grasses (C4) in the stand changed little during the 8-year period, but basal cover and relative amount of cool-season perennial grasses (C3) in the stand declined in the elevated CO2 plots and in ambient CO2 plots with chambers. Forbs (C3) and members of the Cyperaceae (C3) increased in basal cover and relative amount in the stand at elevated compared to ambient CO2. Greater biomass production under elevated CO2 in C4-dominated grasslands may lead to a greater carbon sequestration by those ecosystems and reduce peak atmospheric CO2 concentrations in the future.  相似文献   

11.
We investigated the effects of elevated atmospheric CO2 concentrations (ambient + 200 ppm) on fine root production and soil carbon dynamics in a loblolly pine (Pinus taeda) forest subject to free‐air CO2 enrichment (FACE) near Durham, NC (USA). Live fine root mass (LFR) showed less seasonal variation than dead fine root mass (DFR), which was correlated with seasonal changes in soil moisture and soil temperature. LFR mass increased significantly (by 86%) in the elevated CO2 treatment, with an increment of 37 g(dry weight) m?2 above the control plots after two years of CO2 fumigation. There was no long‐term increment in DFR associated with elevated CO2, but significant seasonal accumulations of DFR mass occurred during the summer of the second year of fumigation. Overall, root net primary production (RNPP) was not significantly different, but annual carbon inputs were 21.7 gC m?2 y?1 (68%) higher in the elevated CO2 treatment compared to controls. Specific root respiration was not altered by the CO2 treatment during most of the year; however, it was significantly higher by 21% and 13% in September 1997 and May 1998, respectively, in elevated CO2. We did not find statistically significant differences in the C/N ratio of the root tissue, root decomposition or phosphatase activity in soil and roots associated with the treatment. Our data show that the early response of a loblolly pine forest ecosystem subject to CO2 enrichment is an increase in its fine root population and a trend towards higher total RNPP after two years of CO2 fumigation.  相似文献   

12.
A fast growing high density Populus plantation located in central Italy was exposed to elevated carbon dioxide for a period of three years. An elevated CO2 treatment (550 ppm), of 200 ppm over ambient (350 ppm) was provided using a FACE technique. Standing root biomass, fine root turnover and mycorrhizal colonization of the following Populus species was examined: Populus alba L., Populus nigra L., Populus x euramericana Dode (Guinier). Elevated CO2 increased belowground allocation of biomass in all three species examined, standing root biomass increased by 47–76% as a result of FACE treatment. Similarly, fine root biomass present in the soil increased by 35–84%. The FACE treatment resulted in 55% faster fine root turnover in P. alba and a 27% increase in turnover of roots of P. nigra and P. x euramericana. P. alba and P. nigra invested more root biomass into deeper soil horizon under elevated CO2. Response of the mycorrhizal community to elevated CO2 was more varied, the rate of infection increased only in P. alba for both ectomycorrhizal (EM) and arbuscular mycorrhizas (AM). The roots of P. nigra showed greater infection only by AM and the colonization of the root system of P. x euramericana was not affected by FACE treatment. The results suggest that elevated atmospheric CO2 conditions induce greater belowground biomass investment, which could lead to accumulation of assimilated C in the soil profile. This may have implications for C sequestration and must be taken into account when considering long‐term C storage in the soil.  相似文献   

13.
Small birch plants were grown for up to 80 d in a climate chamber at varied relative addition rates of nitrogen in culture solution, and at ambient (350 μmol mol-1) or elevated (700 μmol mol-1) concentrations of CO2. The relative addition rate of nitrogen controlled relative growth rate accurately and independently of CO2 concentration at sub-optimum levels. During free access to nutrients, relative growth rate was higher at elevated CO2. Higher values of relative growth rate and net assimilation rate were associated with higher values of plant N-concentration. At all N-supply rates, elevated CO2 resulted in higher values of net assimilation rate, whereas leaf weight ratio was independent of CO2. Specific leaf area (and leaf area ratio) was less at higher CO2 and at lower rates of N-supply. Lower values of specific leaf area were partly because of starch accumulation. Nitrogen productivity (growth rate per unit plant nitrogen) was higher at elevated CO2. At sub-optimal N-supply, the higher net assimilation rate at elevated CO2 was offset by a lower leaf area ratio. Carbon dioxide did not affect root/shoot ratio, but a higher fraction of plant dry weight was found in roots at lower N-supply. In the treatment with lowest N-supply, five times as much root length was produced per amount of plant nitrogen in comparison with optimum plants. The specific fine root length at all N-supplies was greater at elevated CO2. These responses of the root system to lower N-supply and elevated CO2 may have a considerable bearing on the acquisition of nutrients in depleted soils at elevated CO2. The advantage of maintaining steady-state nutrition in small plants while investigating the effects of elevated CO2 on growth is emphasized.  相似文献   

14.
Abstract

Human-induced and natural stress factors can affect fine roots and ectomycorrhizas. Therefore they have potential utility as indicators of environmental change. We evaluated, through meta-analysis, the magnitude of the effects of acidic deposition, nitrogen deposition, increased ozone levels, elevated atmospheric carbon dioxide, and drought on fine roots and ectomycorrhizal (ECM) characteristics. Ectomycorrhizal colonization was an unsuitable parameter for environmental change, but fine root length and biomass could be useful. Acidic deposition had a significantly negative impact on fine roots, root length being more sensitive than root biomass. There were no significant effects of nitrogen deposition or elevated tropospheric ozone on the quantitative root parameters. Elevated CO2 had a significant positive effect. Drought had a significantly negative effect on fine root biomass. The negative effect of acidic deposition and the positive effect of elevated CO2 increased over time, indicating that effects were persistent contrary the other factors. The meta-analysis also showed that experimental conditions, including both laboratory and field experiments, were a major source of variation. In addition to quantitative changes, environmental changes affect the species composition of the ectomycorrhizal fungal community.  相似文献   

15.
The dynamics and demography of roots were followed for 5 years that spanned wet and drought periods in native, semiarid shortgrass steppe grassland exposed to ambient and elevated atmospheric CO2 treatments. Elevated compared with ambient CO2 concentrations resulted in greater root‐length growth (+52%), root‐length losses (+37%), and total pool sizes (+41%). The greater standing pool of roots under elevated compared with ambient CO2 was because of the greater number of roots (+35%), not because individuals were longer. Loss rates increased relatively less than growth rates because life spans were longer (+41%). The diameter of roots was larger under elevated compared with ambient CO2 only in the upper soil profile. Elevated CO2 affected root architecture through increased branching. Growth‐to‐loss ratio regressions to time of equilibrium indicate very long turnover times of 5.8, 7.0, and 5.3 years for control, ambient, and elevated CO2, respectively. Production was greater under elevated compared with ambient CO2 both below‐ and aboveground, and the above‐ to belowground ratios did not differ between treatments. However, estimates of belowground production differed among methods of calculation using minirhizotron data, as well as between minirhizotron and root‐ingrowth methods. Users of minirhizotrons may need to consider equilibration in terms of both new growth and disappearance, rather than just growth. Large temporal pulses of root initiation and termination rates of entire individuals were observed (analogous to birth–death rates), and precipitation explained more of the variance in root initiation than termination. There was a dampening of the pulsing in root initiation and termination under elevated CO2 during both wet and dry periods, which may be because of conservation of soil water reducing the suddenness of wet pulses and duration and severity of dry pulses. However, a very low degree of synchrony was observed between growth and disappearance (production and decomposition).  相似文献   

16.
Elevated CO2 can increase fine root biomass but responses of fine roots to exposure to increased CO2 over many years are infrequently reported. We investigated the effect of elevated CO2 on root biomass and N and P pools of a scrub-oak ecosystem on Merritt Island in Florida, USA, after 7 years of CO2 treatment. Roots were removed from 1-m deep soil cores in 10-cm increments, sorted into different categories (<0.25 mm, 0.25–1 mm, 1–2 mm, 2 mm to 1 cm, >1 cm, dead roots, and organic matter), weighed, and analyzed for N, P and C concentrations. With the exception of surface roots <0.25 mm diameter, there was no effect of elevated CO2 on root biomass. There was little effect on C, N, or P concentration or content with the exception of dead roots, and <0.25 mm and 1–2 mm diameter live roots at the surface. Thus, fine root mass and element content appear to be relatively insensitive to elevated CO2. In the top 10 cm of soil, biomass of roots with a diameter of <0.25 mm was depressed by elevated CO2. Elevated CO2 tended to decrease the mass and N content of dead roots compared to ambient CO2. A decreased N concentration of roots <0.25 mm and 1–2 mm in diameter under elevated CO2 may indicate reduced N supply in the elevated CO2 treatment. Our study indicated that elevated CO2 does not increase fine root biomass or the pool of C in fine roots. In fact, elevated CO2 tends to reduce biomass and C content of the most responsive root fraction (<0.25 mm roots), a finding that may have more general implications for understanding C input into the soil at higher atmospheric CO2 concentrations.  相似文献   

17.
Increased levels of atmospheric carbon dioxide (CO2) are likely to affect the trophic relationships that exist between plants, their herbivores and the herbivores' natural enemies. This study takes advantage of an open‐top CO2 fertilization experiment in a Florida scrub oak community at Kennedy Space Center, Florida, consisting of eight chambers supplied with ambient CO2 (360 ppm) and eight chambers supplied with elevated CO2 (710 ppm). We examined the effects of elevated CO2 on herbivore densities and levels of leaf consumption, rates of herbivore attack by natural enemies and effects on leaf abscission. Cumulative levels of herbivores and herbivore damage were significantly lower in elevated CO2 than in ambient CO2. This may be because leaf nitrogen levels are lower in elevated CO2. More herbivores die of host plant‐induced death in elevated CO2 than in ambient CO2. Attack rates of herbivores by parasitoids are also higher in elevated CO2, possibly because herbivores need to feed for a longer time in order to accrue sufficient nitrogen (N), thus exposing themselves longer to natural enemies. Insect herbivores cause an increase in abscission rates of leaves throughout the year. Because of the lower insect density in elevated CO2, we thought, abscission rates would be lower in these chambers. However, abscission rates were significantly higher in elevated CO2. Thus, the direct effects of elevated CO2 on abscission are greater than the indirect effects on abscission mediated via lower insect densities. A consequence of increased leaf abscission in elevated CO2 is that nutrient deposition rates to the soil surface are accelerated.  相似文献   

18.
The interactive effects of elevated atmospheric CO2 and temperature on seasonal patterns of photosynthesis in Douglas fir (Psuedotsuga menziesii (Mirb.) Franco) seedlings were examined. Seedlings were grown in sunlit chambers controlled to track either ambient (~400 p.p.m.) CO2 or ambient +200 p.p.m. CO2, and either ambient temperature or ambient +4 °C. Light‐saturated net photosynthetic rates were measured approximately monthly over a 21 month period. Elevated CO2 increased net photosynthetic rates by an average of 21% across temperature treatments during both the 1996 hydrologic year, the third year of exposure, and the 1997 hydrologic year. Elevated mean annual temperature increased net photosynthetic rates by an average of 33% across CO2 treatments during both years. Seasonal temperature changes also affected net photosynthetic rates. Across treatments, net photosynthetic rates were highest in the spring and autumn, and lowest in July, August and December–January. Seasonal increases in temperature were not correlated with increases in the relative photosynthetic response to elevated CO2. Seasonal shifts in the photosynthetic temperature optimum reduced temperature effects on the relative response to elevated CO2. These results suggest that the effects of elevated CO2 on net photosynthetic rates in Douglas fir are largely independent of temperature.  相似文献   

19.
Atmospheric carbon dioxide (CO2) and ozone (O3) concentrations are rising, which may have opposing effects on tree C balance and allocation to fine roots. More information is needed on interactive CO2 and O3 effects on roots, particularly fine-root life span, a critical demographic parameter and determinant of soil C and N pools and cycling rates. We conducted a study in which ponderosa pine (Pinus ponderosa) seedlings were exposed to two levels of CO2 and O3 in sun-lit controlled-environment mesocosms for 3 years. Minirhizotrons were used to monitor individual fine roots in three soil horizons every 28 days. Proportional hazards regression was used to analyze effects of CO2, O3, diameter, depth, and season of root initiation on fine-root survivorship. More fine roots were produced in the elevated CO2 treatment than in ambient CO2. Elevated CO2, increasing root diameter, and increasing root depth all significantly increased fine-root survivorship and median life span. Life span was slightly, but not significantly, lower in elevated O3, and increased O3 did not reduce the effect of elevated CO2. Median life spans varied from 140 to 448 days depending on the season of root initiation. These results indicate the potential for elevated CO2 to increase the number of fine roots and their residence time in the soil, which is also affected by root diameter, root depth, and phenology.  相似文献   

20.
Fine roots (≤1 mm diameter) are critical in plant water and nutrient absorption, and it is important to understand how rising atmospheric CO2 will affect them as part of terrestrial ecosystem responses to global change. This study's objective was to determine the effects of elevated CO2 on production, mortality, and standing crops of fine root length over 2 years in a free‐air CO2 enrichment (FACE) facility in the Mojave Desert of southern Nevada, USA. Three replicate 25 m diameter FACE rings were maintained at ambient (~370 μmol mol?1) and elevated CO2 (~550 μmol mol?1) atmospheric concentrations. Twenty‐eight minirhizotron tubes were placed in each ring to sample three microsite locations: evergreen Larrea shrubs, drought‐deciduous Ambrosia shrubs, and along systematic community transects (primarily in shrub interspaces which account for ~85% of the area). Seasonal dynamics were similar for ambient and elevated CO2: fine root production peaked in April–June, with peak standing crop occurring about 1 month later, and peak mortality occurring during the hot summer months, with higher values for all three measures in a wet year compared with a dry year. Fine root standing crop, production, and mortality were not significantly different between treatments except standing crop along community transects, where fine root length was significantly lower in elevated CO2. Fine root turnover (annual cumulative mortality/mean standing crop) ranged from 2.33 to 3.17 year?1, and was not significantly different among CO2 treatments, except for community transect tubes where it was significantly lower for elevated CO2. There were no differences in fine root responses to CO2 between evergreen (Larrea) and drought‐deciduous (Ambrosia) shrubs. Combined with observations of increased leaf‐level water‐use efficiency and lack of soil moisture differences, these results suggest that under elevated CO2 conditions, reduced root systems (compared with ambient CO2) appear sufficient to provide resources for modest aboveground production increases across the community, but in more fertile shrub microsites, fine root systems of comparable size with those in ambient CO2 were required to support the greater aboveground production increases. For community transects, development of the difference in fine root standing crops occurred primarily through lower stimulation of fine root production in the elevated CO2 treatment during periods of high water availability.  相似文献   

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