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1.
* Greater fine-root production under elevated [CO2] may increase the input of carbon (C) and nitrogen (N) to the soil profile because fine root populations turn over quickly in forested ecosystems. * Here, the effect of elevated [CO)] was assessed on root biomass and N inputs at several soil depths by combining a long-term minirhizotron dataset with continuous, root-specific measurements of root mass and [N]. The experiment was conducted in a CO(2)-enriched sweetgum (Liquidambar styraciflua) plantation. * CO2) enrichment had no effect on root tissue density or [N] within a given diameter class. Root biomass production and standing crop were doubled under elevated [CO2]. Though fine-root turnover declined under elevated [CO2], fine-root mortality was also nearly doubled under CO2 enrichment. Over 9 yr, root mortality resulted in 681 g m(-2) of extra C and 9 g m(-2) of extra N input to the soil system under elevated [CO2]. At least half of these inputs were below 30 cm soil depth. * Increased C and N input to the soil under CO2 enrichment, especially below 30 cm depth, might alter soil C storage and N mineralization. Future research should focus on quantifying root decomposition dynamics and C and N mineralization deeper in the soil.  相似文献   

2.
We conducted a 4-year study of juvenile Pinus ponderosa fine root (≤2 mm) responses to atmospheric CO2 and N-fertilization. Seedlings were grown in open-top chambers at three CO2 levels (ambient, ambient+175 μmol/mol, ambient+350 μmol/mol) and three N-fertilization levels (0, 10, 20 g m−2 year−1). Length and width of individual roots were measured from minirhizotron video images bimonthly over 4 years starting when the seedlings were 1.5 years old. Neither CO2 nor N-fertilization treatments affected the seasonal patterns of root production or mortality. Yearly values of fine-root length standing crop (m m−2), production (m m−2 year−1), and mortality (m m−2 year−1) were consistently higher in elevated CO2 treatments throughout the study, except for mortality in the first year; however, the only statistically significant CO2 effects were in the fine-root length standing crop (m m−2) in the second and third years, and production and mortality (m m−2 year−1) in the third year. Higher mortality (m m−2 year−1) in elevated CO2 was due to greater standing crop rather than shorter life span, as fine roots lived longer in elevated CO2. No significant N effects were noted for annual cumulative production, cumulative mortality, or mean standing crop. N availability did not significantly affect responses of fine-root standing crop, production, or mortality to elevated CO2. Multi-year studies at all life stages of trees are important to characterize belowground responses to factors such as atmospheric CO2 and N-fertilization. This study showed the potential for juvenile ponderosa pine to increase fine-root C pools and C fluxes through root mortality in response to elevated CO2.  相似文献   

3.
The Rhinelander free-air CO(2) enrichment (FACE) experiment is designed to understand ecosystem response to elevated atmospheric carbon dioxide (+CO(2)) and elevated tropospheric ozone (+O(3)). The objectives of this study were: to understand how soil respiration responded to the experimental treatments; to determine whether fine-root biomass was correlated to rates of soil respiration; and to measure rates of fine-root turnover in aspen (Populus tremuloides) forests and determine whether root turnover might be driving patterns in soil respiration. Soil respiration was measured, root biomass was determined, and estimates of root production, mortality and biomass turnover were made. Soil respiration was greatest in the +CO(2) and +CO(2) +O(3) treatments across all three plant communities. Soil respiration was correlated with increases in fine-root biomass. In the aspen community, annual fine-root production and mortality (g m(-2)) were positively affected by +O(3). After 10 yr of exposure, +CO(2) +O(3)-induced increases in belowground carbon allocation suggest that the positive effects of elevated CO(2) on belowground net primary productivity (NPP) may not be offset by negative effects of O(3). For the aspen community, fine-root biomass is actually stimulated by +O(3), and especially +CO(2) +O(3).  相似文献   

4.
Climate change (elevated atmospheric CO2, and altered air temperatures, precipitation amounts and seasonal patterns) may affect ecosystem processes by altering carbon allocation in plants, and carbon flux from plants to soil. Mycorrhizal fungi, as carbon sinks, are among the first soil biota to receive carbon from plants, and thereby influence carbon release from plants to soil. One step in this carbon release is via fine root and mycorrhizal turnover. It is necessary to know the lifetime and temporal occurrence of roots and mycorrhizae to determine the capacity of the soil ecosystem to sequester carbon assimilated aboveground. In this study, ponderosa pine (Pinus ponderosa Laws) seedlings were grown under three levels of atmospheric CO2 (ambient, 525 and 700 mol CO2 mol-1) and three levels of annual nitrogen additions (0,100 and 200 kg N ha-1) in open-top chambers. At a two-month frequency during 18 months, we observed ectomycorrhizal root tips observed using minirhizotron tubes and camera. The numbers of new mycorrhizal root tips, the numbers of tips that disappeared between two consecutive recording events, and the standing crop of tips at each event were determined. There were more mycorrhizal tips of all three types seen during the summer compared with other times of the year. When only the standing crop of mycorrhizal tips was considered, effects of the CO2 and N addition treatments on carbon allocation to mycorrhizal tips was weakly evident. However, when the three types of tips were considered collectively, tips numbers flux of carbon through mycorrhizae was greatest in the: (1) high CO2 treatment compared with the other CO2 treatments, and (2) intermediate N addition treatment compared with the other N addition treatments. A survival analysis on the entire 18 month cohort of tips was done to calculate the median lifetime of the mycorrhizal root tips. Average median lifetime of the mycorrhizal tips was 139 days and was not affected by nitrogen and CO2 treatments.  相似文献   

5.
The research described in this paper represents a part of a much broader research project with the general objective of describing the effects of elevated [CO2] and temperature on tree growth, physiological processes, and ecosystem-level processes. The specific objective of this research was to examine the below-ground respiratory responses of sugar maple (Acer saccharum Marsh.) and red maple (Acer rubrum L.) seedlings to elevated atmospheric [CO2] and temperature. Red maple and sugar maple seedlings were planted in the ground in each of 12 open-top chambers and exposed from 1994 through 1997 to ambient air or air enriched with 30 Pa CO2,< in combination with ambient or elevated (+4 °C) air temperatures. Carbon dioxide efflux was measured around the base of the seedlings and from root-exclusion zones at intervals during 1995 and 1996 and early 1997. The CO2 efflux rates averaged 0.4 μmol CO2 m-2 s-1 in the root-exclusion zones and 0.75 μmol CO2 m-2 s-1 around the base of the seedlings. Mineral soil respiration in root-exclusion zones averaged 12% higher in the high temperature treatments than at ambient temperature, but was not affected by CO2 treatments. The fraction of total efflux attributable to root + rhizosphere respiration ranged from 14 to 61% in measurements made around red maple plants, and from 35 to 62% around sugar maple plants. Root respiration rates ranged from 0 to 0.94 μmol CO2 s-1 m-2 of soil surface in red maple and from 0 to 1.02 in sugar maple. In both 1995 and 1996 root respiration rates of red maple were highest in high-CO2 treatments and lowest in high temperature treatments. Specific red maple root respiration rates of excised roots from near the soil surface in 1996 were also highest under CO2 enrichment and lowest in high temperature treatments. In sugar maple the highest rates of CO2 efflux were from around the base of plants exposed to both high temperature and high-CO2, even though specific respiration rates were< lowest for this species under the high temperature and CO2 enrichment regime. In both species, patterns of response to treatments were similar in root respiration and root mass, indicating that the root respiration responses were due in part to differences in root mass. The results underscore the need for separating the processes occurring in the roots from those in the forest floor and mineral soil in order to increase our understanding of the effects of global climate change on carbon sequestration and cycling in the below-ground systems of forests.  相似文献   

6.
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   

7.
Elevated CO2 and conifer roots: effects on growth, life span and turnover   总被引:5,自引:4,他引:1  
Elevated CO2 increases root growth and fine (diam. 2 mm) root growth across a range of species and experimental conditions. However, there is no clear evidence that elevated CO2 changes the proportion of C allocated to root biomass, measured as either the root:shoot ratio or the fine root:needle ratio. Elevated CO2 tends to increase mycorrhizal infection, colonization and the amount of extramatrical hyphae, supporting their key role in aiding the plant to more intensively exploit soil resources, providing a route for increased C sequestration. Only two studies have determined the effects of elevated CO2 on conifer fine-root life span, and there is no clear trend. Elevated CO2 increases the absolute fine-root turnover rates; however, the standing crop root biomass is also greater, and the effect of elevated CO2 on relative turnover rates (turnover:biomass) ranges from an increase to a decrease. At the ecosystem level these changes could lead to increased C storage in roots. Increased fine-root production coupled with increased absolute turnover rates could also lead to increases in soil organic C as greater amounts of fine roots die and decompose. Although CO2 can stimulate fine-root growth, it is not known if this stimulation persists over time. Modeling studies suggest that a doubling of the atmospheric CO2 concentration initially increases biomass, but this stimulation declines with the response to elevated CO2 because increases in assimilation are not matched by increases in nutrient supply.  相似文献   

8.
Fine root production and turnover play important roles in regulating carbon (C) cycling in terrestrial ecosystems. In order to examine effects of climate change on root production and turnover, a field experiment with increased temperature and precipitation had been conducted in a semiarid temperate steppe in northern China since April 2005. Experimental warming decreased annual root production, mortality, and mean standing crop by 10.3%, 12.1%, 7.0%, respectively, while root turnover was not affected in 2006 and 2007 by the warming. Annual root production and turnover was 5.9% and 10.3% greater in the elevated than ambient precipitation plots. Changes in root production and mortality in response to increased temperature and precipitation could be largely attributed to the changes in gross ecosystem productivity (GEP) and belowground/aboveground C allocation. There were significant interactive effects of warming and increased precipitation on root productivity, mortality, and standing crop. Experimental warming had positive and negative effects on the three root variables (root production, mortality, standing crop) under ambient and increased precipitation, respectively. Increased precipitation stimulated and suppressed the three root variables in the unwarmed and warmed subplots, respectively. The positive dependence of soil respiration and ecosystem respiration upon root productivity and mortality highlights the important role of root dynamics in ecosystem C cycling. The nonadditive effects of increased temperature and precipitation on root productivity, mortality, and standing crop observed in this study are critical for model projections of climate–ecosystem feedbacks. These findings indicate that carbon allocation is a focal point for future research and that results from single factor experiments should be treated with caution because of factor interactions.  相似文献   

9.
Root dynamics are important for plant, ecosystem and global carbon cycling. Changes in root dynamics caused by rising atmospheric CO2 not only have the potential to moderate further CO2 increases, but will likely affect forest function. We used FACE (Free‐Air CO2 Enrichment) to expose three 30‐m diameter plots in a 13‐year‐old loblolly pine (Pinus taeda) forest to elevated (ambient + 200 µL L?1) atmospheric CO2. Three identical fully instrumented plots were implemented as controls (ambient air only). We quantified root dynamics from October 1998 to October 1999 using minirhizotrons. In spite of 16% greater root lengths and 24% more roots per minirhizotron tube, the effects of elevated atmospheric CO2 on root lengths and numbers were not statistically significant. Similarly, production and mortality were also unaffected by the CO2 treatment, even though annual root production and mortality were 26% and 46% greater in elevated compared to ambient CO2 plots. Average diameters of live roots present at the shallowest soil depth were, however, significantly enhanced in CO2‐enriched plots. Mortality decreased with increasing soil depth and the slopes of linear regression lines (mortality vs. depth) differed between elevated and ambient CO2 treatments, reflecting the significant CO2 by depth interaction. Relative root turnover (root flux/live root pool) was unchanged by exposure to elevated atmospheric CO2. Results from this study suggest modest, if any, increases in ecosystem‐level root productivity in CO2‐enriched environments.  相似文献   

10.
唐国  胡雷  宋小艳  李香真  王长庭 《生态学报》2022,42(15):6250-6264
根系是草原生态系统中最重要的碳库之一,分析高寒草甸植物群落生物量和地下不同径级根系碳分配特征及根系的生长特征对降雨变化的响应,有利于了解全球变化背景下高寒草甸植物根系、土壤碳氮循环及其过程。采用微根管技术原位监测5种降雨处理下(增雨50%:1.5P、自然降雨:1.0P、减雨30%:0.7P、减雨50%:0.5P、减雨90%:0.1P)高寒草甸植物群落和根系属性(现存量、生产量、死亡量、根系寿命和周转速率)的变化特征,结果表明:(1)降雨变化对地上植物群落生物量无显著影响,但0.5P和0.1P显著增加禾本科生物量(P<0.05)。(2)总根系现存量在处理间无显著差异,但随着降雨量减少呈先增加后降低的趋势。土层间不同径级根系现存量差异显著,0-10 cm土层1.5P和0.7P1级根现存量显著增加,2级和3级根现存量显著降低;在10-20 cm土层,1.0P2级根系现存量显著高于其余处理(P<0.05)。(3)总根生产量与死亡量随降雨减少而降低,在0-10 cm土层,1.0P总根生产量和死亡量最高,0.1P显著降低了1级根生产量(P<0.05)。(4)0.1P显著增加10-20 cm土层1级根和总根寿命(P<0.05)。(5)根系周转随降雨量减少呈降低趋势,但无显著差异(P>0.05)。(6)结构方程模型进一步表明:根系现存量和生产量受土层和水分的直接影响,土层和养分对根系周转有负效应。综上所述,降雨量的变化并未显著改变地下总根系生物量,但少量降雨变化(0.7P、1.5P)会降低植物对2、3级根生物量的分配,投入更多资源以促进1级根的生长;而水分下降至轻度水分胁迫(0.1P),植物会减少地下各径级根系生物量的分配,保持低根系生物量消耗和低根系生长来维持其正常的生长状态,完成其正常的生态功能。  相似文献   

11.
利用封顶式生长室模拟未来变化的气候条件,研究了亚高山林线优势物种岷江冷杉(Abies faxoniana)和4种草本植物形态与竞争指标对CO2浓度和温度升高的响应.结果表明:处理2个生长季后,高CO2浓度条件下,岷江冷杉冠体积增加42%,比叶面积、比冠体积和比根长分别增加17%、65%和19%;温度升高使岷江冷杉冠形更纵向生长,冠体积增加22%,根冠比和比根长均比对照增加17%;二者同时升高使岷江冷杉冠体积增加79%,比叶面积、比冠体积和比根长分别增加17%、197%和18%.CO2浓度升高处理下糙野青茅(Deyeuxia scabrescen)的株高、基茎和每株叶片数增加,但比叶面积降低;甘肃苔草(Carexkansuensis)、东方草莓(Fragaria orientali)和紫花碎米荠(Cardamine tangutorum)的各项指标变化与青茅相反.温度升高下青茅、苔草、草莓株高、基茎和根冠比下降.二者同时升高条件下4种草本植物的基茎和每株叶片数增加,但比叶面积和根冠比降低.这表明,在CO2浓度和温度升高处理下,岷江冷杉形成有利于生长的冠层结构且单位质量的竞争力增加,而4种草本植物的形态结构和竞争力均受到不同程度的负面影响.  相似文献   

12.
Applications and limitations of the minirhizotron technique (non-destructive) in relation to two frequently used destructive methods (soil coreing and ingrowth cores) is discussed. Sequential coreing provides data on standing crop but it is difficult to obtain data on root biomass production. Ingrowth cores can provide a quick estimate of relative fine-root growth when root growth is rapid. One limitation of the ingrowth core is that no information on the time of ingrowth and mortality is obtained.The minirhizotron method, in contrast to the destructive methods permits simultaneous calculation of fine-root length production and mortality and turnover. The same fine-root segment in the same soil space can be monitored for its life time, and stored in a database for processing. The methodological difficulties of separating excavated fine roots into living and dead vitality classes are avoided, since it is possible to judge directly the successive ageing of individual roots from the images. It is concluded that the minirhizotron technique is capable of quantifying root dynamics (root-length production, mortality and longevity) and fine-root decomposition. Additionally, by combining soil core data (biomass, root length and nutrient content) and minirhizotron data (length production and mortality), biomass production and nutrient input into the soil via root mortality and decomposition can be estimated.  相似文献   

13.
Efforts to characterize carbon (C) cycling among atmosphere, forest canopy, and soil C pools are hindered by poorly quantified fine root dynamics. We characterized the influence of free‐air‐CO2‐enrichment (ambient +200 ppm) on fine roots for a period of 6 years (Autumn 1998 through Autumn 2004) in an 18‐year‐old loblolly pine (Pinus taeda) plantation near Durham, NC, USA using minirhizotrons. Root production and mortality were synchronous processes that peaked most years during spring and early summer. Seasonality of fine root production and mortality was not influenced by atmospheric CO2 availability. Averaged over all 6 years of the study, CO2 enrichment increased average fine root standing crop (+23%), annual root length production (+25%), and annual root length mortality (+36%). Larger increase in mortality compared with production with CO2 enrichment is explained by shorter average fine root lifespans in elevated plots (500 days) compared with controls (574 days). The effects of CO2‐enrichment on fine root proliferation tended to shift from shallow (0–15 cm) to deeper soil depths (15–30) with increasing duration of the study. Diameters of fine roots were initially increased by CO2‐enrichment but this effect diminished over time. Averaged over 6 years, annual fine root NPP was estimated to be 163 g dw m?2 yr?1 in CO2‐enriched plots and 130 g dw m?2 yr?1 in control plots (P= 0.13) corresponding to an average annual additional input of fine root biomass to soil of 33 g m?2 yr?1 in CO2‐enriched plots. A lack of consistent CO2× year effects suggest that the positive effects of CO2 enrichment on fine root growth persisted 6 years following minirhizotron tube installation (8 years following initiation of the CO2 fumigation). Although CO2‐enrichment contributed to extra flow of C into soil in this experiment, the magnitude of the effect was small suggesting only modest potential for fine root processes to directly contribute to soil C storage in south‐eastern pine forests.  相似文献   

14.
Experimental increases in atmospheric CO? often increase root production over time, potentially increasing soil carbon (C) sequestration. Effects of elevated atmospheric CO? on fine root dynamics in a Mojave desert ecosystem were examined for the last 4.5 yr of a long-term (10-yr) free air CO? enrichment (FACE) study at the Nevada desert FACE facility (NDFF). Sets of minirhizotron tubes were installed at the beginning of the NDFF experiment to characterize rooting dynamics of the dominant shrub Larrea tridentata, the codominant shrub Ambrosia dumosa and the plant community as a whole. Although significant treatment effects occurred sporadically for some fine root measurements, differences were transitory and often in opposite directions during other time-periods. Nonetheless, earlier root growth under elevated CO? helped sustain increased assimilation and shoot growth. Overall CO? treatment effects on fine root standing crop, production, loss, turnover, persistence and depth distribution were not significant for all sampling locations. These results were similar to those that occurred near the beginning of the NDFF experiment but unlike those in other ecosystems. Thus, increased C input into soils is unlikely to occur from fine root litter under elevated atmospheric CO? in this arid ecosystem.  相似文献   

15.
We investigated the effects of elevated soil temperature and atmospheric CO2 on soil CO2 efflux (SCE) during the third and fourth years of study. We hypothesized that elevated temperature would stimulate SCE, and elevated CO2 would also stimulate SCE with the stimulation being greater at higher temperatures. The study was conducted in sun-lit controlled-environment chambers using Douglas-fir (Pseudotsuga menziesii) seedlings grown in reconstructed litter-soil systems. We used a randomized design with two soil temperature and two atmospheric CO2 treatments. The SCE was measured every 4 wk for 18 months. Neither elevated temperature nor CO2 stimulated SCE. Elevated CO2 increased the temperature sensitivity of SCE. During the winter, the relationship between SCE and soil moisture was negative but it was positive during the summer. The seasonal patterns in SCE were associated with seasonal changes in photosynthesis and above-ground plant growth. SCE acclimatized in the high-temperature treatment, probably because of a loss of labile soil carbon. Elevated CO2 treatment increased the temperature sensitivity of SCE, probably through an increase in substrate availability.  相似文献   

16.
Differential responses to elevated atmospheric CO(2) concentration exhibited by different plant functional types may alter competition for above- and belowground resources in a higher CO(2) world. Because C allocation to roots is often favored over C allocation to shoots in plants grown with CO(2) enrichment, belowground function of forest ecosystems may change significantly. We established an outdoor facility to examine the effects of elevated CO(2) on root dynamics in artificially constructed communities of five early successional forest species: (1) a C(3) evergreen conifer (longleaf pine, Pinus palustris Mill.); (2) a C(4) monocotyledonous bunch grass (wiregrass, Aristida stricta Michx.); (3) a C(3) broadleaf tree (sand post oak, Quercus margaretta); (4) a C(3) perennial herbaceous legume (rattlebox, Crotalaria rotundifolia Walt. ex Gemel); and (5) an herbaceous C(3) dicotyledonous perennial (butterfly weed, Asclepias tuberosa L.). These species are common associates in early successional longleaf pine savannahs throughout the southeastern USA and represent species that differ in life-form, growth habit, physiology, and symbiotic relationships. A combination of minirhizotrons and soil coring was used to examine temporal and spatial rooting dynamics from October 1998 to October 1999. CO(2)-enriched plots exhibited 35% higher standing root crop length, 37% greater root length production per day, and 47% greater root length mortality per day. These variables, however, were enhanced by CO(2) enrichment only at the 10-30 cm depth. Relative root turnover (flux/standing crop) was unchanged by elevated CO(2). Sixteen months after planting, root biomass of pine was 62% higher in elevated compared to ambient CO(2) plots. Conversely, the combined biomass of rattlebox, wiregrass, and butterfly weed was 28% greater in ambient compared to high CO(2) plots. There was no difference in root biomass of oaks after 16 months of exposure to elevated CO(2). Using root and shoot biomass as a metric, longleaf pine realized the greatest and most consistent benefit from exposure to elevated CO(2). This finding suggests that the ability of longleaf pine to compete with sand post oak, a common deciduous tree competitor, and wiregrass, the dominant understory herbaceous species, in regenerating ecosystems may be significantly enhanced by rising atmospheric CO(2) concentrations.  相似文献   

17.
Optimal nitrogen allocation controls tree responses to elevated CO2   总被引:1,自引:0,他引:1  
Despite the abundance of experimental data, understanding of forest responses to elevated CO2 is limited. Here I show that a key to previously unexplained production and leaf area responses lies in the interplay between whole-plant nitrogen (N) allocation and leaf photosynthesis. A simple tree growth model, controlled by net growth maximization through optimization of leaf area index (LAI) and plant N, is used to analyse CO2 responses in both young, expanding and closed, steady-state canopies. The responses are sensitive to only two independent parameters, the photosynthetic capacity per leaf N (a) and the fine-root N:leaf N ratio. The model explains observed CO2 responses of photosynthesis, production and LAI in four forest free air CO2 enrichment (FACE) experiments. Insensitivity of LAI except at low LAI, increase in light-use efficiency, and photosynthetic down-regulation (as a result of reduced leaf N per area) at elevated CO2 are all explained through the combined effects on a and leaf quantum efficiency. The model bridges the gap between the understanding of leaf-level and plant-level responses and provides a transparent framework for interpreting and linking structural (LAI) and functional (net primary production (NPP):gross primary production (GPP) ratio, light-use efficiency, photosynthetic down-regulation) responses to elevated CO2.  相似文献   

18.
Elevated CO2, rhizosphere processes,and soil organic matter decomposition   总被引:12,自引:0,他引:12  
Cheng  Weixin  Johnson  Dale W. 《Plant and Soil》1998,202(2):167-174
The rhizosphere is one of the key fine-scale components of C cycles. This study was undertaken to improve understanding of the potential effects of atmospheric CO2 increase on rhizosphere processes. Using C isotope techniques, we found that elevated atmospheric CO2 significantly increased wheat plant growth, dry mass accumulation, rhizosphere respiration, and soluble C concentrations in the rhizosphere. When plants were grown under elevated CO2 concentration, soluble C concentration in the rhizosphere increased by approximately 60%. The degree of elevated CO2 enhancement on rhizosphere respiration was much higher than on root biomass. Averaged between the two nitrogen treatments and compared with the ambient CO2 treatment, wheat rhizosphere respiration rate increased 60% and root biomass only increased 26% under the elevated CO2 treatment. These results indicated that elevated atmospheric CO2 in a wheat-soil system significantly increased substrate input to the rhizosphere due to both increased root growth and increased root activities per unit of roots. Nitrogen treatments changed the effect of elevated CO2 on soil organic matter decomposition. Elevated CO2 increased soil organic matter decomposition (22%) in the nitrogen-added treatment but decreased soil organic matter decomposition (18%) without nitrogen addition. Soil nitrogen status was therefore found to be important in determining the directions of the effect of elevated CO2 on soil organic matter decomposition.  相似文献   

19.
Soil fungi couple plant and ecosystem resource demands to pools of soil resources. Research on these organisms is needed to predict how rising atmospheric CO2 will influence forest ecosystem processes and soil carbon (C) sequestration potential. We examined the influence of free‐air‐CO2‐enrichment (FACE) on mycorrhizal and extraradical rhizomorph dynamics over a 5‐year period in a loblolly pine forest using minirhizotrons. Standing crop of mycorrhizal root tips varied greatly spatially and through time. Summed across all years, CO2 enrichment increased mycorrhizal root tip production by 194% in deep soil (15–30 cm) but did not influence mycorrhizal production in shallow soil (0–15 cm). Production and mortality of soil rhizomorph length was 27% and 25% greater in CO2‐enriched plots compared with controls over a 5‐year period beginning in January of 2000 and running through autumn 2004. Effects of atmospheric CO2 enrichment on longevity of mycorrhizal root tips and rhizomorphs varied with soil depth (mycorrhizae and rhizomorphs) and with diameter (rhizomorphs). For instance, survival of mycorrhizal tips was reduced in CO2‐enriched plots in deep soil (15–30 cm depth) but was increased in shallower soil (0–15 cm). Rhizomorph turnover was accelerated in shallow soil but effects on survivorship in deep soil varied according to diameter. A drought in 2002 coupled with loss of leaf area to an ice storm late in 2002 were followed by reductions in rhizomorph and mycorrhizal production, increases in mortality, and decreases in standing crop during 2003 and 2004. These effects tended to be more severe in CO2‐enriched plots. Positive effects of atmospheric CO2 enrichment on mycorrhizal fungi, primarily observed in deeper soil, are probably contributing to the prolonged stimulation of NPP by CO2 enrichment at the Duke FACE study site.  相似文献   

20.
Water table fluctuation in arid land regions may alter tree fine-root growth and mortality, thereby affecting leaf growth. To reveal the effects of water table fluctuation on fine-root growth and mortality and their relation to leaf growth, we exposed P. alba L. cuttings to various fluctuating water table depths. 1-year-old rooted cuttings were grown individually in pots containing sandy soil in a greenhouse in three water table depth treatments for 45 days: constant depth at 45 cm from the soil surface, fluctuating depths between 45 and 30 cm, and fluctuating depths between 45 and 15 cm. Fine-root biomass and mortality, biomass partitioning among plant parts, and whole-tree growth responses were determined in cuttings harvested every 15 days. Fluctuation of water tables increased the mortality of fine roots at the layers near the soil surface. Fine-root mortality increased during the shallower water table depth period. At the whole-root system level, although fine-root mortality increased when the water table was shallower, fine-root biomass was similar among the treatments, suggesting that P. alba cuttings would sustains its standing fine-root biomass under fluctuating water table depth conditions. Our structural equation modeling showed the fine-root proportion affects leaf morphological changes, suggesting that there would be a parallel relationship of morphological changes between roots and leaves with fluctuating water tables.  相似文献   

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