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1.
干扰对典型草原生态系统土壤净呼吸特征的影响   总被引:1,自引:0,他引:1  
由于土地利用格局的改变和人类干扰活动的加剧,草地生态系统CO2排放与固定的平衡、碳循环特征以及碳储量越来越受到人们的重视。尤其是定量区分土壤净呼吸与土壤总呼吸量之间的比例关系,以及定量描述草地生态系统碳循环过程等方面的研究尚不够完善。以河北沽源的典型草原为研究对象,测定了火烧、灌溉、施肥、刈割干扰下的天然草地土壤净呼吸变化动态及其与主要控制因素之间的关系。结果表明:不同处理土壤净呼吸均表现出明显的季节性变化规律,变化趋势基本一致。火烧、灌溉和刈割处理分别比对照的土壤净呼吸通量降低了28.93%、16.25%和36.82%。土壤温度、土壤湿度与土壤净呼吸通量呈指数相关(P0.01)。对地上生物量、地下生物量、土壤有机碳含量和土壤全氮含量与土壤净呼吸之间进行逐步回归分析表明,土壤有机碳含量(SC)和土壤全氮含量(SN)是土壤净呼吸通量的主要影响因素。  相似文献   

2.
The spatial and temporal variations of soil respiration were studied from May 2004 to June 2005 in a C3/C4 mixed grassland of Japan. The linear regression relationship between soil respiration and root biomass was used to determine the contribution of root respiration to soil respiration. The highest soil respiration rate of 11-54 Μmol m-2 s-1 was found in August 2004 and the lowest soil respiration rate of 4.99 Μmol m-2 s-1 was found in April 2005. Within-site variation was smaller than seasonal change in soil respiration. Root biomass varied from 0.71 kg m-2 in August 2004 to 102 in May 2005. Within-site variation in root biomass was larger than seasonal variation. Root respiration rate was highest in August 2004 (5.7 Μmol m-2 s-1) and lowest in October 2004 (1.7 Μmol m-2 s-1). Microbial respiration rate was highest in August 2004 (5.8 Μmol m-2 s-1) and lowest in April 2005 (2.59 Μmol m-2 s-1). We estimated that the contribution of root respiration to soil respiration ranged from 31% in October to 51% in August of 2004, and from 45% to 49% from April to June 2005.  相似文献   

3.
4.
草地土壤固碳潜力研究进展   总被引:6,自引:3,他引:6  
戴尔阜  黄宇  赵东升 《生态学报》2015,35(12):3908-3918
土壤固碳功能和固碳潜力已成为全球气候变化和陆地生态系统研究的重点。草地土壤有机碳库,作为陆地土壤有机碳库的重要组成部分,其较小幅度的波动,将会影响整个陆地生态系统碳循环,进而影响全球气候变化。因此,深入研究草地土壤固碳功能和固碳潜力对于适应和减缓气候变化具有重要意义。在土壤固碳潜力相关概念界定基础上,结合《2006年IPCC国家温室气体清单指南》,从样点及区域尺度上综述了目前关于草地土壤固碳潜力的一般估算方法,同时对各类方法的特点及适用性进行了评述,提出了草地生态系统固碳潜力研究概念模型。最后在对草地土壤固碳的影响因素及固碳措施总结的基础上,阐明了草地土壤有机碳固定研究中存在的问题和发展前景。  相似文献   

5.
A trenching method was used to determine the contribution of root respiration to soil respiration. Soil respiration rates in a trenched plot (R trench) and in a control plot (R control) were measured from May 2000 to September 2001 by using an open-flow gas exchange system with an infrared gas analyser. The decomposition rate of dead roots (R D) was estimated by using a root-bag method to correct the soil respiration measured from the trenched plots for the additional decaying root biomass. The soil respiration rates in the control plot increased from May (240–320 mg CO2 m–2 h–1) to August (840–1150 mg CO2 m–2 h–1) and then decreased during autumn (200–650 mg CO2 m–2 h–1). The soil respiration rates in the trenched plot showed a similar pattern of seasonal change, but the rates were lower than in the control plot except during the 2 months following the trenching. Root respiration rate (R r) and heterotrophic respiration rate (R h) were estimated from R control, R trench, and R D. We estimated that the contribution of R r to total soil respiration in the growing season ranged from 27 to 71%. There was a significant relationship between R h and soil temperature, whereas R r had no significant correlation with soil temperature. The results suggest that the factors controlling the seasonal change of respiration differ between the two components of soil respiration, R r and R h.  相似文献   

6.
Radiocarbon (14C) provides a measure of the mean age of carbon (C) in roots, or the time elapsed since the C making up root tissues was fixed from the atmosphere. Radiocarbon signatures of live and dead fine (<2 mm diameter) roots in two mature Amazon tropical forests are consistent with average ages of 4–11 years (ranging from <1 to >40 years). Measurements of 14C in the structural tissues of roots known to have grown during 2002 demonstrate that new roots are constructed from recent (<2‐year‐old) photosynthetic products. High Δ14C values in live roots most likely indicate the mean lifetime of the root rather than the isotopic signature of inherited C or C taken up from the soil. Estimates of the mean residence time of C in forest fine roots (inventory divided by loss rate) are substantially shorter (1–3 years) than the age of standing fine root C stocks obtained from radiocarbon (4–11 years). By assuming positively skewed distributions for root ages, we can effectively decouple the mean age of C in live fine roots (measured using 14C) from the rate of C flow through the live root pool, and resolve these apparently disparate estimates of root C dynamics. Explaining the 14C values in soil pore space CO2, in addition, requires that a portion of the decomposing roots be cycled through soil organic matter pools with decadal turnover time.  相似文献   

7.
CO2 flux from the soil was measured in situ under oil palms in southern Benin. The experimental design took into account the spatial variability of the root density, the organic matter in the soil-palm agrosystem and the effect of factors such as the soil temperature and moisture.Measurements of CO2 release in situ, and a comparison with the results obtained in the laboratory from the same soil free of roots, provided an estimation of the roots contribution to the total CO2 flux. The instantaneous values for total release in situ were between 3.2 and 10.0 mol CO2 m-2 s-1. For frond pile zones rich in organic matter, and around oil palm trunks, root respiration accounted for 30% of the efflux when the soil was at field capacity and 80% when the soil was dry with a pF close to 4.2. This proportion remained constant in interrow zones at around 75%, irrespective of soil moisture.Subsequently carbon allocation to the roots was determined. Total CO2 release over a year was 57 Mg of CO2 ha-1 yr-1 (around 1610 g of C per m2 per year), and carbon allocation to the roots was approximately 53 Mg of CO2 ha-1 yr-1 of which approximately 13 Mg CO2 ha-1 yr-1 (25%) was devoted to turn-over and 40 Mg CO2 ha-1 yr-1 (75%) to respiration.  相似文献   

8.
Soil respiration (Rs) is a major pathway by which fixed carbon in the biosphere is returned to the atmosphere, yet there are limits to our ability to predict respiration rates using environmental drivers at the global scale. While temperature, moisture, carbon supply, and other site characteristics are known to regulate soil respiration rates at plot scales within certain biomes, quantitative frameworks for evaluating the relative importance of these factors across different biomes and at the global scale require tests of the relationships between field estimates and global climatic data. This study evaluates the factors driving Rs at the global scale by linking global datasets of soil moisture, soil temperature, primary productivity, and soil carbon estimates with observations of annual Rs from the Global Soil Respiration Database (SRDB). We find that calibrating models with parabolic soil moisture functions can improve predictive power over similar models with asymptotic functions of mean annual precipitation. Soil temperature is comparable with previously reported air temperature observations used in predicting Rs and is the dominant driver of Rs in global models; however, within certain biomes soil moisture and soil carbon emerge as dominant predictors of Rs. We identify regions where typical temperature‐driven responses are further mediated by soil moisture, precipitation, and carbon supply and regions in which environmental controls on high Rs values are difficult to ascertain due to limited field data. Because soil moisture integrates temperature and precipitation dynamics, it can more directly constrain the heterotrophic component of Rs, but global‐scale models tend to smooth its spatial heterogeneity by aggregating factors that increase moisture variability within and across biomes. We compare statistical and mechanistic models that provide independent estimates of global Rs ranging from 83 to 108 Pg yr?1, but also highlight regions of uncertainty where more observations are required or environmental controls are hard to constrain.  相似文献   

9.
尽管干旱区生态系统的脆弱性受到了广泛的关注, 但目前关于干旱区植物细根有机碳与土壤碳循环关系的研究还比较少见。在2010年整个生长季节内, 采用土钻法和内生长法, 对新疆干旱区的琵琶柴(Reaumuria soongorica)群落土壤特性、细根的生物量月动态、生产量和周转进行了研究。结果表明: 琵琶柴群落表层土壤含水量最低, 土壤含水量表现出从浅层到深层逐渐增加的趋势; 而表层土壤的有机碳含量最高, 随着土壤深度的加深, 有机碳含量逐渐降低。细根生物量的月平均值为54.51 g·m-2, 群落细根生产量在82.76-136.21 g·m-2·a-1之间, 琵琶柴群落的细根周转率为2.08 times·a-1, 通过细根死亡进入土壤中的有机碳为17 g·m-2·a-1。这些结果表明: 由于灌丛细根高的周转速率, 细根是干旱区土壤有机碳输入的重要部分。  相似文献   

10.
Huang  Bingru  Fu  Jinmin 《Plant and Soil》2000,227(1-2):17-26
The study was conducted to investigate carbon metabolic responses to surface soil drying for cool-season grasses. Kentucky bluegrass (Poa pratensis L.) and tall fescue (Festuca arundinaceae Schreb.) were grown in a greenhouse in split tubes consisting of two sections. Plants were subjected to three soil moisture regimes: (1) well-watered control; (2) drying of upper 20-cm soil (upper drying); and (3) drying of whole 40-cm soil profile (full drying). Upper drying for 30 d had no dramatic effects on leaf water potential (Ψleaf) and canopy photosynthetic rate (Pn) in either grass species compared to the well-watered control, but it reduced canopy respiration rate (Rcanopy) and root respiration rate in the top 20 cm of soil (Rtop). For both species in the lower 20 cm of wet soil, root respiration rates (Rbottom) were similar to the control levels, and carbon allocation to roots increased with the upper soil drying, particularly for tall fescue. The proportion of roots decreased in the 0-20 cm drying soil, but increased in the lower 20 cm wet soil for both grass species; the increase was greater for tall fescue. The Ψleaf, Pn, Rcanopy, Rtop, Rbottom, and carbon allocation to roots in both soil layers were all significantly higher for upper dried plants than for fully dried plants of both grass species. The reductions in Rcanopy and Rtop in surface drying soil and increases in root respiration and carbon allocation to roots in lower wet soil could help these grasses cope with surface-soil drought stress. This revised version was published online in June 2006 with corrections to the Cover Date.  相似文献   

11.
Soil respiration was measured for 2 years in an artificial gap and in an undisturbed area in a Japanese cedar (Cryptomeria japonica D. Don) forest to estimate the contribution of root respiration to total soil respiration. Measurement plots were set up at the center of the gap, the edge of the gap, the edge of the surrounding stand and within the stand. Using a small gap (2.5 m × 2.5 m) enabled us to maintain the same soil temperature and soil moisture as found in the stand. Seasonal fluctuations in soil respiration, increasing in summer and decreasing in winter, corresponded to changes in the soil surface temperature. Soil respiration in the gap site did not differ significantly from those in the stand in the first year of gap formation. However, in the second year, the minimum CO2 flux was observed at the center of the gap and the maximum at the edge of the surrounding stand. Assuming that the differences between soil respiration in the center of the gap and that in the stand were equal to the root respiration, the root respiration rate was calculated from the relationship between the root respiration rates (Rr) and the soil surface temperature (Ts) by Ln(Rr) = 0.07Ts + 3.48. The average contribution of root respiration to total soil respiration, as estimated from the soil surface temperature in the stand by using the above equation, was 49%. After taking root decomposition into consideration, the contribution of root respiration to soil respiration increased from 49 to 57%.  相似文献   

12.
Warming temperatures are likely to accelerate permafrost thaw in the Arctic, potentially leading to the release of old carbon previously stored in deep frozen soil layers. Deeper thaw depths in combination with geomorphological changes due to the loss of ice structures in permafrost, may modify soil water distribution, creating wetter or drier soil conditions. Previous studies revealed higher ecosystem respiration rates under drier conditions, and this study investigated the cause of the increased ecosystem respiration rates using radiocarbon signatures of respired CO2 from two drying manipulation experiments: one in moist and the other in wet tundra. We demonstrate that higher contributions of CO2 from shallow soil layers (0–15 cm; modern soil carbon) drive the increased ecosystem respiration rates, while contributions from deeper soil (below 15 cm from surface and down to the permafrost table; old soil carbon) decreased. These changes can be attributed to more aerobic conditions in shallow soil layers, but also the soil temperature increases in shallow layers but decreases in deep layers, due to the altered thermal properties of organic soils. Decreased abundance of aerenchymatous plant species following drainage in wet tundra reduced old carbon release but increased aboveground plant biomass elevated contributions of autotrophic respiration to ecosystem respiration. The results of this study suggest that drier soils following drainage may accelerate decomposition of modern soil carbon in shallow layers but slow down decomposition of old soil carbon in deep layers, which may offset some of the old soil carbon loss from thawing permafrost.  相似文献   

13.
Oil palm (Elaeis guineensis Jacq.) crops are expanding rapidly in the tropics, with implications for the global carbon cycle. Little is currently known about soil organic carbon (SOC) dynamics following conversion to oil palm and virtually nothing for conversion of grassland. We measured changes in SOC stocks following conversion of tropical grassland to oil palm plantations in Papua New Guinea using a chronosequence of plantations planted over a 25‐year period. We further used carbon isotopes to quantify the loss of grassland‐derived and gain in oil palm‐derived SOC over this period. The grassland and oil palm soils had average SOC stocks of 10.7 and 12.0 kg m?2, respectively, across all the study sites, to a depth of 1.5 m. In the 0–0.05 m depth interval, 0.79 kg m?2 of SOC was gained from oil palm inputs over 25 years and approximately the same amount of the original grass‐derived SOC was lost. For the whole soil profile (0–1.5 m), 3.4 kg m?2 of SOC was gained from oil palm inputs with no significant losses of grass‐derived SOC. The grass‐derived SOC stocks were more resistant to decrease than SOC reported in other studies. Black carbon produced in grassfires could partially but not fully account for the persistence of the original SOC stocks. Oil palm‐derived SOC accumulated more slowly where soil nitrogen contents where high. Forest soils in the same region had smaller carbon stocks than the grasslands. In the majority of cases, conversion of grassland to oil palm plantations in this region resulted in net sequestration of soil organic carbon.  相似文献   

14.
Black carbon (BC) is an important pool of the global C cycle, because it cycles much more slowly than others and may even be managed for C sequestration. Using stable isotope techniques, we investigated the fate of BC applied to a savanna Oxisol in Colombia at rates of 0, 11.6, 23.2 and 116.1 t BC ha?1, as well as its effect on non‐BC soil organic C. During the rainy seasons of 2005 and 2006, soil respiration was measured using soda lime traps, particulate and dissolved organic C (POC and DOC) moving by saturated flow was sampled continuously at 0.15 and 0.3 m, and soil was sampled to 2.0 m. Black C was found below the application depth of 0–0.1 m in the 0.15–0.3 m depth interval, with migration rates of 52.4±14.5, 51.8±18.5 and 378.7±196.9 kg C ha?1 yr?1 (±SE) where 11.6, 23.2 and 116.1 t BC ha?1, respectively, had been applied. Over 2 years after application, 2.2% of BC applied at 23.2 t BC ha?1 was lost by respiration, and an even smaller fraction of 1% was mobilized by percolating water. Carbon from BC moved to a greater extent as DOC than POC. The largest flux of BC from the field (20–53% of applied BC) was not accounted for by our measurements and is assumed to have occurred by surface runoff during intense rain events. Black C caused a 189% increase in aboveground biomass production measured 5 months after application (2.4–4.5 t additional dry biomass ha?1 where BC was applied), and this resulted in greater amounts of non‐BC being respired, leached and found in soil for the duration of the experiment. These increases can be quantitatively explained by estimates of greater belowground net primary productivity with BC addition.  相似文献   

15.
以菜地和果园土壤为研究对象,通过室内培养实验,向土壤中分别添加不同材料制备的生物炭(马尼拉草、阔叶和竹叶),热解温度为350℃,研究不同材料制备生物炭添加对土壤呼吸和有机碳含量的影响.结果表明:不同生物炭施入土壤后,土壤 CO 2释放速率总的趋势是前期分解速率快,后期缓慢.在整个培养过程中(28 d),随着培养时间的延长,土壤 CO 2释放速率下降趋势逐渐降低.在不同土壤培养条件下,均是添加阔叶生物炭后土壤 CO 2-C 累计释放增多,果园和菜地土壤 CO 2-C 累计分别达到482.57和424.72 mg·kg-1.添加不同的生物炭均能提高土壤有机碳含量,但只有添加阔叶生物炭之后,差异才会达到显著(P <0.05).研究结果为正确利用生物炭和评价其在土壤碳库作用提供科学依据.  相似文献   

16.
以安徽省滁州市红琊山林场麻栎人工林为研究对象,测定了4种施肥处理(0、0.15、0.30和0.45kg·株-1)林分碳密度,并采用开沟隔离法对不同处理林分休眠期土壤呼吸组分进行测定。结果表明:4种施肥处理林分总碳密度分别为73.68、84.49、87.20和91.70t·hm-2。与对照相比,各施肥处理麻栎树干碳密度、树枝碳密度和枯落物碳密度均有极显著提高(P<0.01)。不同处理林分的土壤总呼吸速率和异养呼吸速率随着施肥量增加呈递增趋势,施肥量为0.45kg·株-1样地土壤总呼吸速率和异养呼吸速率较对照样地分别增加了48.9%和38.6%。不同施肥样地土壤异养呼吸对土壤总呼吸的贡献率远大于根系呼吸,施肥量为0、0.15、0.30和0.45kg·株-1时分别是根系呼吸的5.0、3.8、3.4和3.2倍。土壤呼吸受生物因子和非生物因子共同调控,在所选取的4个指标中(土壤含水量、土壤C/N、根生物量和枯落物有机碳含量),土壤含水量和枯落物有机碳含量与土壤总呼吸及土壤异养呼吸速率均有显著相关性(P<0.05)。  相似文献   

17.
郭丽娟  国庆喜 《生态学报》2013,33(13):4090-4100
IBIS模型是陆地碳循环模拟的有利工具,土壤呼吸是陆地碳循环的关键生态学过程,利用IBIS模型模拟估算土壤呼吸对陆地碳循环和全球变化研究具有重要意义.在地形数据、植被参数、土壤质地参数和气象数据支持下,利用改造后的IBIS模型模拟2004年张家沟集水区5种森林类型的土壤呼吸,以实测数据对模拟结果进行验证,并分析土壤呼吸时空格局及其与土壤温湿度的关系.结果表明:(1)改造后的IBIS模型模拟的土壤呼吸值与实测值相关性显著,可较好地用于集水区尺度的森林土壤呼吸模拟估算.(2)土壤呼吸年均值为571 gCm-2 a-1,年土壤呼吸空间格局与生长季土壤呼吸空间格局相似,均表现为高值区主要分布在北部、西南和东南区域,低值区主要分布在沟谷附近,该格局与集水区的地形、植被及其组合等因素有关.(3)生长季内,5种森林类型土壤呼吸的季节性变化均呈单峰曲线形式,土壤呼吸峰值均出现在7月,其中落叶松林峰值最低,为85.5gC/m2,杂木林峰值最高,为146.3 gC/m2.(4)5种森林类型的土壤呼吸值与5 cm深土壤温度存在极显著的指数关系,与土壤湿度的相关性较低,土壤温度的变化可以解释土壤呼吸约70%的季节变化.  相似文献   

18.
基于4月底到9月底东北地区玉米农田土壤呼吸作用全生长季的观测,阐明了土壤呼吸作用的空间异质性特征,综合分析了水热因子、土壤性质、根系生物量及其测定位置对土壤呼吸作用空间异质性的影响,并对生长季中根系呼吸作用占土壤呼吸作用的比例进行了估算。结果表明,在植株尺度上,土壤呼吸作用存在着明显的空间异质性,较高的土壤呼吸速率通常出现在靠近玉米植株的地方。根系生物量的分布格局是影响土壤呼吸作用空间异质性的关键因素。在空间尺度上,土壤呼吸作用与根系生物量呈显著的线性关系,而土壤湿度、土壤有机质、全氮和碳氮比对土壤呼吸作用空间异质性的影响并不显著。通过建立土壤呼吸作用与玉米根系生物量的回归方程,对根系呼吸作用占土壤呼吸作用的比例进行了间接估算。玉米生长季中,根系呼吸作用占土壤呼吸作用的比例在43.1%~63.6%之间波动,均值为54.5%。  相似文献   

19.
This experiment was designed to study three determinant factors in decomposition patterns of soil organic matter (SOM): temperature, water and carbon (C) inputs. The study combined field measurements with soil lab incubations and ends with a modelling framework based on the results obtained. Soil respiration was periodically measured at an oak savanna woodland and a ponderosa pine plantation. Intact soils cores were collected at both ecosystems, including soils with most labile C burnt off, soils with some labile C gone and soils with fresh inputs of labile C. Two treatments, dry‐field condition and field capacity, were applied to an incubation that lasted 111 days. Short‐term temperature changes were applied to the soils periodically to quantify temperature responses. This was done to prevent confounding results associated with different pools of C that would result by exposing treatments chronically to different temperature regimes. This paper discusses the role of the above‐defined environmental factors on the variability of soil C dynamics. At the seasonal scale, temperature and water were, respectively, the main limiting factors controlling soil CO2 efflux for the ponderosa pine and the oak savanna ecosystems. Spatial and seasonal variations in plant activity (root respiration and exudates production) exerted a strong influence over the seasonal and spatial variation of soil metabolic activity. Mean residence times of bulk SOM were significantly lower at the Nitrogen (N)‐rich deciduous savanna than at the N‐limited evergreen dominated pine ecosystem. At shorter time scales (daily), SOM decomposition was controlled primarily by temperature during wet periods and by the combined effect of water and temperature during dry periods. Secondary control was provided by the presence/absence of plant derived C inputs (exudation). Further analyses of SOM decomposition suggest that factors such as changes in the decomposer community, stress‐induced changes in the metabolic activity of decomposers or SOM stabilization patterns remain unresolved, but should also be considered in future SOM decomposition studies. Observations and confounding factors associated with SOM decomposition patterns and its temperature sensitivity are summarized in the modeling framework.  相似文献   

20.
Forest soil respiration is the sum of heterotrophic (microbes, soil fauna) and autotrophic (root) respiration. The contribution of each group needs to be understood to evaluate implications of environmental change on soil carbon cycling and sequestration. Three primary methods have been used to distinguish hetero- versus autotrophic soil respiration including: integration of components contributing to in situ forest soil CO2 efflux (i.e., litter, roots, soil), comparison of soils with and without root exclusion, and application of stable or radioactive isotope methods. Each approach has advantages and disadvantages, but isotope based methods provide quantitative answers with the least amount of disturbance to the soil and roots. Published data from all methods indicate that root/rhizosphere respiration can account for as little as 10 percent to greater than 90 percent of total in situ soil respiration depending on vegetation type and season of the year. Studies which have integrated percent root contribution to total soil respiration throughout an entire year or growing season show mean values of 45.8 and 60.4 percent for forest and nonforest vegetation, respectively. Such average annual values must be extrapolated with caution, however, because the root contribution to total soil respiration is commonly higher during the growing season and lower during the dormant periods of the year.  相似文献   

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