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1.
Jian Ni 《Folia Geobotanica》2001,36(2):113-129
A biome classification for China was established based on plant functional types (PFTs) using the BIOME3 model to include 16 biomes. In the eastern part of China, the PFTs of trees determine mostly the physiognomy of landscape. Biomes range from boreal deciduous coniferous forest/woodland, boreal mixed forest/woodland, temperate mixed forest, temperate broad-leaved deciduous forest, warm-temperate broad-leaved evergreen/mixed forest, warm-temperate/cool-temperate evergreen coniferous forest, xeric woodland/scrub, to tropical seasonal and rain forest, and tropical deciduous forest from north to south. In the northern and western part of China, grass is the dominant PFT. From northeast to west and southwest the biomes range from moist savannas, tall grassland, short grassland, dry savannas, arid shrubland/steppe, desert, to alpine tundra/ice/polar desert. Comparisons between the classification introduced here and the four classifications which were established over the past two decades, i.e. the vegetation classification, the vegetation division, the physical ecoregion, and the initial biome classification have showed that the different aims of biome classifications have resulted in different biome schemes each with its own unique characteristics and disadvantages for global change study. The new biome classification relies not only on climatic variables, but also on soil factor, vegetation functional variables, ecophysiological parameters and competition among the PFTs. It is a comprehensive classification that using multivariables better expresses the vegetation distribution and can be compared with world biome classifications. It can be easily used in the response study of Chinese biomes to global change, regionally and globally.  相似文献   

2.
BIOME 6000 is an international project to map vegetation globally at mid‐Holocene (6000 14C yr bp ) and last glacial maximum (LGM, 18,000 14C yr bp ), with a view to evaluating coupled climate‐biosphere model results. Primary palaeoecological data are assigned to biomes using an explicit algorithm based on plant functional types. This paper introduces the second Special Feature on BIOME 6000. Site‐based global biome maps are shown with data from North America, Eurasia (except South and Southeast Asia) and Africa at both time periods. A map based on surface samples shows the method’s skill in reconstructing present‐day biomes. Cold and dry conditions at LGM favoured extensive tundra and steppe. These biomes intergraded in northern Eurasia. Northern hemisphere forest biomes were displaced southward. Boreal evergreen forests (taiga) and temperate deciduous forests were fragmented, while European and East Asian steppes were greatly extended. Tropical moist forests (i.e. tropical rain forest and tropical seasonal forest) in Africa were reduced. In south‐western North America, desert and steppe were replaced by open conifer woodland, opposite to the general arid trend but consistent with modelled southward displacement of the jet stream. The Arctic forest limit was shifted slighly north at 6000 14C yr bp in some sectors, but not in all. Northern temperate forest zones were generally shifted greater distances north. Warmer winters as well as summers in several regions are required to explain these shifts. Temperate deciduous forests in Europe were greatly extended, into the Mediterranean region as well as to the north. Steppe encroached on forest biomes in interior North America, but not in central Asia. Enhanced monsoons extended forest biomes in China inland and Sahelian vegetation into the Sahara while the African tropical rain forest was also reduced, consistent with a modelled northward shift of the ITCZ and a more seasonal climate in the equatorial zone. Palaeobiome maps show the outcome of separate, independent migrations of plant taxa in response to climate change. The average composition of biomes at LGM was often markedly different from today. Refugia for the temperate deciduous and tropical rain forest biomes may have existed offshore at LGM, but their characteristic taxa also persisted as components of other biomes. Examples include temperate deciduous trees that survived in cool mixed forest in eastern Europe, and tropical evergreen trees that survived in tropical seasonal forest in Africa. The sequence of biome shifts during a glacial‐interglacial cycle may help account for some disjunct distributions of plant taxa. For example, the now‐arid Saharan mountains may have linked Mediterranean and African tropical montane floras during enhanced monsoon regimes. Major changes in physical land‐surface conditions, shown by the palaeobiome data, have implications for the global climate. The data can be used directly to evaluate the output of coupled atmosphere‐biosphere models. The data could also be objectively generalized to yield realistic gridded land‐surface maps, for use in sensitivity experiments with atmospheric models. Recent analyses of vegetation‐climate feedbacks have focused on the hypothesized positive feedback effects of climate‐induced vegetation changes in the Sahara/Sahel region and the Arctic during the mid‐Holocene. However, a far wider spectrum of interactions potentially exists and could be investigated, using these data, both for 6000 14C yr bp and for the LGM.  相似文献   

3.
Net primary production, carbon storage and climate change in Chinese biomes   总被引:1,自引:0,他引:1  
Net primary production (NPP) and leaf area index (LAI) of Chinese biomes were simulated by BIOME3 under the present climate, and their responses to climate change and doubled CO2 under a future climatic scenario using output from Hadley Center coupled ocean‐atmosphere general circulation model with CO2 modelled at 340 and 500 ppmv. The model estimated annual mean NPP of the biomes in China to be between 0 and 1270.7 gC m‐2 yr‐1 at present. The highest productivity was found in tropical seasonal and rain forests while temperate forests had an intermediate NPP, which is higher than a lower NPP of temperate savannas, grasslands and steppes. The lowest NPP occurred in desert, alpine tundra and ice/polar desert in cold or arid regions, especially on the Tibetan Plateau. The lowest monthly NPP of each biome occurred generally in February and the highest monthly NPP occurred during the summer (June to August). The annual mean NPP and LAI of most of biomes at changed climate with CO2 at 340 and 500 ppmv (direct effects on physiology) would be greater than present. The direct effects of carbon dioxide on plant physiology result in significant increase of LAI and NPP. The carbon storage of Chinese biomes at present and changed climates was calculated by the carbon density and vegetation area method. The present estimates of carbon storage are totally 175.83 × 1012 gC (57.57 × 1012 gC in vegetation and 118.28 × 1012 gC in soils). Changed climate without and with the CO2 direct physiological effects will result in an increase of carbon storage of 5.1 and 16.33 × 1012, gC compared to present, respectively. The interaction between elevated CO2 and climate change plays an important role in the overall responses of NPP and carbon to climate change.  相似文献   

4.
Ecogeographical regionalization is the basis for spatial differentiation of biodiversity research. In view of the principle of international ecogeographical regionalization, this study has applied multivariate analysis and GIS method and based on some ecogeographical attributes limited to the distribution of plant and vegetation, including climatic factors, such as minimum temperature, mean temperature of the coldest month, mean temperature of the wannest month, annual average temperature, precipitation of the coldest month, precipitation of the wannest month, annual precipitation, CV of annual precipitation, biological factors such as vegetation types, vegetation division types, NPP, fiorisitic types, fauna types, abundance of plant species, genus and endemic genus; soil factors such as soil types, soil pH;topographical factors as longitude, latitude and altitude etc. The ecogeographical regionalization for biodiversity in China was made synthetically by using fuzzy cluster method. Four classes of division were used, viz., biodomain, subbiodomain, biome and bioregion. Five biodomains, seven subbiodomains and eighteen biomes were divided in China as follows: Ⅰ Boreal forest biodomain. Ⅰ A Eurasian boreal forest subbiodomain. Ⅰ A1 Southern Taiga mountain cold-temperate coniferous forest biome; Ⅰ A2 North Asian mixed coniferous-broad-leaved forest biome. Ⅱ Northern steppe and desert biodomain. Ⅱ B Eurasian steppe subbiodomain. Ⅱ BI Inner Asian temperate grass steppe biome; Ⅱ B2 Loess Plateau warm-temperate forest/shmb steppe biome. Ⅱ C Asia-Mrica desert subbiodomain. Ⅱ C1 Mid-Asian temperate desert biome; Ⅱ C2 Mongolian/Inner Asian temperate desert biome. Ⅲ East Asian biodomain. Ⅲ D East Asian deciduous broad-leaved forest subbiodomain. Ⅲ D1 East Asian deciduous broad-leaved forest biome, Ⅲ E East Asian evergreen broad-leaved forest subbiodomain. Ⅲ El East Asian mixed deciduous-evergreen broad-leaved forest biome; Ⅲ E2 East Asian evergreen broad-leaved forest biome; Ⅲ E3 East Asian monsoon evergreen broad-leaved forest biome; Ⅲ FA Western East Asian mountain evergreen broadleaved forest biome. Ⅳ Palaeotropical subdomain. IV F India-Malaysian tropical forest subbiodomain.Ⅳ Fl Northern tropical rain forest/seasonal rain forest biome; Ⅳ F2 Tropical island coral reef vegetation biome. Ⅴ Asian plateau biodomain. Ⅴ G Tibet Plateau subbiodomain. Ⅴ G1 Tibet alpine highcold shrub meadow biome;Ⅴ G2 Tibet alpine high-cold steppe biome; Ⅴ G3 Tibet alpine high-cold desert biome; Ⅴ G4 Tibet alpine temperate steppe biome; Ⅴ G5 Tibet alpine temperate desert biome.  相似文献   

5.
Aim To produce a robust, comprehensive global biome reconstruction for the Middle Pliocene (c. 3.6–2.6 Ma), which is based on an internally consistent palaeobotanical data set and a state‐of‐the‐art coupled climate–vegetation model. The reconstruction gives a more rigorous picture of climate and environmental change during the Middle Pliocene and provides a new boundary condition for future general circulation model (GCM) studies. Location Global. Methods Compilation of Middle Pliocene vegetation data from 202 marine and terrestrial sites into the comprehensive GIS data base TEVIS (Tertiary Environmental Information System). Translation into an internally consistent classification scheme using 28 biomes. Comparison and synthesis of vegetation reconstruction from palaeodata with the outputs of the mechanistically based BIOME4 model forced by climatology derived from the HadAM3 GCM. Results The model results compare favourably with available palaeodata and highlight the importance of employing vegetation–climate feedbacks and the anomaly method in biome models. Both the vegetation reconstruction from palaeobotanical data and the BIOME4 prediction indicate a general warmer and moister climate for the Middle Pliocene. Evergreen taiga as well as temperate forest and grassland shifted northward, resulting in much reduced tundra vegetation. Warm‐temperate forests (with subtropical taxa) spread in mid and eastern Europe and tropical savannas and woodland expanded in Africa and Australia at the expense of deserts. Discrepancies which occurred between data reconstruction and model simulation can be related to: (1) poor spatial model resolution and data coverage; (2) uncertainties in delimiting biomes using climate parameters; or (3) uncertainties in model physics and/or geological boundary conditions. Main conclusions The new global biome reconstruction combines vegetation reconstruction from palaeobotanical proxies with model simulations. It is an important contribution to the further understanding of climate and vegetation changes during the Middle Pliocene warm interval and will enhance our knowledge about how vegetation may change in the future.  相似文献   

6.
Pollen data from China for 6000 and 18,000 14C yr bp were compiled and used to reconstruct palaeovegetation patterns, using complete taxon lists where possible and a biomization procedure that entailed the assignment of 645 pollen taxa to plant functional types. A set of 658 modern pollen samples spanning all biomes and regions provided a comprehensive test for this procedure and showed convincing agreement between reconstructed biomes and present natural vegetation types, both geographically and in terms of the elevation gradients in mountain regions of north‐eastern and south‐western China. The 6000 14C yr bp map confirms earlier studies in showing that the forest biomes in eastern China were systematically shifted northwards and extended westwards during the mid‐Holocene. Tropical rain forest occurred on mainland China at sites characterized today by either tropical seasonal or broadleaved evergreen/warm mixed forest. Broadleaved evergreen/warm mixed forest occurred further north than today, and at higher elevation sites within the modern latitudinal range of this biome. The northern limit of temperate deciduous forest was shifted c. 800 km north relative to today. The 18,000 14C yr bp map shows that steppe and even desert vegetation extended to the modern coast of eastern China at the last glacial maximum, replacing today’s temperate deciduous forest. Tropical forests were excluded from China and broadleaved evergreen/warm mixed forest had retreated to tropical latitudes, while taiga extended southwards to c. 43°N.  相似文献   

7.
The global vegetation response to climate and atmospheric CO2 changes between the last glacial maximum and recent times is examined using an equilibrium vegetation model (BIOME4), driven by output from 17 climate simulations from the Palaeoclimate Modelling Intercomparison Project. Features common to all of the simulations include expansion of treeless vegetation in high northern latitudes; southward displacement and fragmentation of boreal and temperate forests; and expansion of drought‐tolerant biomes in the tropics. These features are broadly consistent with pollen‐based reconstructions of vegetation distribution at the last glacial maximum. Glacial vegetation in high latitudes reflects cold and dry conditions due to the low CO2 concentration and the presence of large continental ice sheets. The extent of drought‐tolerant vegetation in tropical and subtropical latitudes reflects a generally drier low‐latitude climate. Comparisons of the observations with BIOME4 simulations, with and without consideration of the direct physiological effect of CO2 concentration on C3 photosynthesis, suggest an important additional role of low CO2 concentration in restricting the extent of forests, especially in the tropics. Global forest cover was overestimated by all models when climate change alone was used to drive BIOME4, and estimated more accurately when physiological effects of CO2 concentration were included. This result suggests that both CO2 effects and climate effects were important in determining glacial‐interglacial changes in vegetation. More realistic simulations of glacial vegetation and climate will need to take into account the feedback effects of these structural and physiological changes on the climate.  相似文献   

8.
Aim The study examined the potential for change in biome representation within Canada's national park system under multiple climate change scenarios and subsequent potential vulnerabilities in Parks Canada policy and planning frameworks. Location The study was conducted for Canada's 39 national parks. Methods The vegetation change scenarios were based on modelling results from the BIOME3 and MAPSS equilibrium process‐based global vegetation models (GVM), run with multiple doubled‐CO2 climate change scenarios. The six vegetation distribution scenarios were calculated at 0.5° latitude–longitude resolution and the boundaries of 39 national parks superimposed in a geographic information system (GIS). Park management plans and other planning documents were also reviewed as part of the analysis. Results The proportional distribution of biomes in Canada's national park system was very similar (within 3% of area for each biome) using BIOME3 and MAPSS under the current climate. Regardless of the GVM and climate change scenario used, the modelling results suggest the potential for substantial change in the biome representation in Canada's national park system. In five of six vegetation scenarios, a novel biome type appeared in more than half of the national parks and greater than 50% of all vegetation grid boxes changed biome type. The proportional representation of tundra and taiga/tundra in the national park system declined in each of the vegetation scenarios, while more southerly biomes (temperate forests and savanna/woodland) increased (in some scenarios doubling to quadrupling). Results for boreal forest varied among the climate change scenarios. A range of potential vulnerabilities in existing policy and planning frameworks were identified, including the national park system plan, individual park objectives, and fire and exotic species management plans. Conclusions Climate change represents an unprecedented challenge to Parks Canada and its ability to achieve its conservation mandate as presently legislated. Research is needed not only on ecosystem responses to climate change, but also on the capacity of conservation systems and agencies to adapt to climate change.  相似文献   

9.
Understanding spring phenology changes in response to the rapid climate change at biome‐level is crucial for projecting regional ecosystem carbon exchange and climate–biosphere interactions. In this study, we assessed the long‐term changes and responses to changing climate of the spring phenology in six temperate biomes of China by analyzing the global inventory monitoring and modeling studies (GIMMS) NOAA/AVHRR Normalized Difference Vegetation Index (NDVI) and concurrent mean temperature and precipitation data for 1982–2006. Results show that the spring phenology trends in the six temperate biomes are not continuous throughout the 25 year period. The spring phenology in most areas of the six biomes showed obvious advancing trends (ranging from ?0.09 to ?0.65 day/yr) during the 1980s and early 1990s, but has subsequently suffered consistently delaying trends (ranging from 0.22 to 1.22 day/yr). Changes in spring (February–April) temperature are the dominating factor governing the pattern of spring vegetation phenology in the temperate biomes of China. The recently delayed spring phenology in these temperate biomes has been mainly triggered by the stalling or reversal of the warming trend in spring temperatures. Results in this study also reveal that precipitation during November–January can explain 16.1% (< 0.05), 20.9% (< 0.05) and 14.2% (< 0.05) of the variations in temperate deciduous forest (TDF), temperate steppe (TS), temperate desert (TD) respectively, highlighting the important role of winter precipitation in regulating changes in the spring vegetation phenology of water–limited biomes.  相似文献   

10.
Aim Climate change threatens to shift vegetation, disrupting ecosystems and damaging human well‐being. Field observations in boreal, temperate and tropical ecosystems have detected biome changes in the 20th century, yet a lack of spatial data on vulnerability hinders organizations that manage natural resources from identifying priority areas for adaptation measures. We explore potential methods to identify areas vulnerable to vegetation shifts and potential refugia. Location Global vegetation biomes. Methods We examined nine combinations of three sets of potential indicators of the vulnerability of ecosystems to biome change: (1) observed changes of 20th‐century climate, (2) projected 21st‐century vegetation changes using the MC1 dynamic global vegetation model under three Intergovernmental Panel on Climate Change (IPCC) emissions scenarios, and (3) overlap of results from (1) and (2). Estimating probability density functions for climate observations and confidence levels for vegetation projections, we classified areas into vulnerability classes based on IPCC treatment of uncertainty. Results One‐tenth to one‐half of global land may be highly (confidence 0.80–0.95) to very highly (confidence ≥ 0.95) vulnerable. Temperate mixed forest, boreal conifer and tundra and alpine biomes show the highest vulnerability, often due to potential changes in wildfire. Tropical evergreen broadleaf forest and desert biomes show the lowest vulnerability. Main conclusions Spatial analyses of observed climate and projected vegetation indicate widespread vulnerability of ecosystems to biome change. A mismatch between vulnerability patterns and the geographic priorities of natural resource organizations suggests the need to adapt management plans. Approximately a billion people live in the areas classified as vulnerable.  相似文献   

11.
利用孢粉记录定量重建大尺度古植被格局   总被引:1,自引:1,他引:0       下载免费PDF全文
陈瑜  倪健 《植物生态学报》2008,32(5):1201-1212
 古植被定量重建是过去全球变化研究的重点之一, 生物群区化(Biomisation)方法以特征植物功能型来定义生物群区, 通过一种标准化数量方法计算孢粉谱的相似得分, 以此把孢粉谱转变为生物群区类型, 是进行古植被定量重建的一种有效方法。该文在前人综述文章的基础上, 简述了生物群区化方法定量重建古植被格局的发展历史、具体步骤及存在问题, 重点描述了以此方法为基础重建的全新世中期(MH)和末次盛冰期(LGM)的全球古植被分布格局, 以及中国的古植被定量重建工作和古植被格局变化。目前的研究表明, 全新世中期北极森林界线在某些地区有轻微的北移迹象, 北部的温带森林带通常向北远距离迁移, 欧洲的温带落叶林也大范围向地中海地区(向南)和向北扩展, 在北美内陆, 草原侵入到森林生物群区, 但中亚地区却没有此现象, 中国大陆的森林生物群区扩张, 典型撒哈尔植被(如干草原、干旱疏林灌丛和热带干旱森林)进入撒哈拉地区, 而非洲热带雨林却呈减少趋势; 末次盛冰期苔原和草原扩张, 在欧亚大陆北部逐渐混合, 北半球的森林生物群区向南迁移, 北方常绿森林(泰加林)和温带落叶林呈碎片状, 而欧洲和东亚的草原却大范围扩张, 非洲的热带湿润森林(比如热带雨林和热带季雨林)有所减少, 在北美洲的西南地区, 荒漠和草原被开阔针叶疏林所取代。  相似文献   

12.
Aim The goals of this study are: (1) to determine whether increasing atmospheric CO2 concentrations and changing climate increased intrinsic water use efficiency (iWUE, as detected by changes in Δ13C) over the last four decades; and if it did increase iWUE, whether it led to increased tree growth (as measured by tree‐ring growth); (2) to assess whether CO2 responses are biome dependent due to different environmental conditions, including availability of nutrients and water; and (3) to discuss how the findings of this study can better inform assumptions of CO2 fertilization and climate change effects in biospheric and climate models. Location A global range of sites covering all major forest biome types. Methods The analysis encompassed 47 study sites including boreal, wet temperate, mediterranean, semi‐arid and tropical biomes for which measurements of tree ring Δ13C and growth are available over multiple decades. Results The iWUE inferred from the Δ13C analyses of comparable mature trees increased 20.5% over the last 40 years with no significant differences between biomes. This increase in iWUE did not translate into a significant overall increase in tree growth. Half of the sites showed a positive trend in growth while the other half had a negative or no trend. There were no significant trends within biomes or among biomes. Main conclusions These results show that despite an increase in atmospheric CO2 concentrations of over 50 p.p.m. and a 20.5% increase in iWUE during the last 40 years, tree growth has not increased as expected, suggesting that other factors have overridden the potential growth benefits of a CO2‐rich world in many sites. Such factors could include climate change (particularly drought), nutrient limitation and/or physiological long‐term acclimation to elevated CO2. Hence, the rate of biomass carbon sequestration in tropical, arid, mediterranean, wet temperate and boreal ecosystems may not increase with increasing atmospheric CO2 concentrations as is often implied by biospheric models and short‐term elevated CO2 experiments.  相似文献   

13.
The response of natural vegetation to climate change is of global concern. In this research, changes in the spatial pattern of major terrestrial ecosystems from 1956 to 2006 in Inner Mongolia of China were analyzed with the Holdridge Life Zone (HLZ) model in a GIS environment, and net primary production (NPP) of natural vegetation was evaluated with the Synthetic model, to determine the effect of climate change on the ecosystem. The results showed that climate warming and drying strongly influenced ecosystems. Decreased precipitation and the subsequent increase in temperature and potential evapotranspiration caused a severe water deficiency, and hence decreased ecosystem productivity. Climate change also influenced the spatial distribution of HLZs. In particular, new HLZs began to appear, such as Warm temperate desert scrub in 1981 and Warm temperate thorn steppe in 2001. The relative area of desert (Cool temperate desert scrub, Warm temperate thorn steppe, Warm temperate desert scrub, Cool temperate desert and Warm temperate desert) increased by 50.2% over the last half century, whereas the relative area of forest (Boreal moist forest and Cool moist forest) decreased by 36.5%. Furthermore, the area of Cool temperate steppe has continuously decreased at a rate of 5.7% per decade; if the current rate of decrease continues, this HLZ could disappear in 173 years. The HLZs had a large shift range with the mean center of the relative life zones of desert shifting northeast, resulting a decrease in the steppe and forest area and an increase in the desert area. In general, a strong effect of climate change on ecosystems was indicated. Therefore, the important role of climate change must be integrated into rehabilitation strategies of ecosystem degradation of Inner Mongolia.  相似文献   

14.
Forest age, which is affected by stand‐replacing ecosystem disturbances (such as forest fires, harvesting, or insects), plays a distinguishing role in determining the distribution of carbon (C) pools and fluxes in different forested ecosystems. In this synthesis, net primary productivity (NPP), net ecosystem productivity (NEP), and five pools of C (living biomass, coarse woody debris, organic soil horizons, soil, and total ecosystem) are summarized by age class for tropical, temperate, and boreal forest biomes. Estimates of variability in NPP, NEP, and C pools are provided for each biome‐age class combination and the sources of variability are discussed. Aggregated biome‐level estimates of NPP and NEP were higher in intermediate‐aged forests (e.g., 30–120 years), while older forests (e.g., >120 years) were generally less productive. The mean NEP in the youngest forests (0–10 years) was negative (source to the atmosphere) in both boreal and temperate biomes (?0.1 and –1.9 Mg C ha?1 yr?1, respectively). Forest age is a highly significant source of variability in NEP at the biome scale; for example, mean temperate forest NEP was ?1.9, 4.5, 2.4, 1.9 and 1.7 Mg C ha?1 yr?1 across five age classes (0–10, 11–30, 31–70, 71–120, 121–200 years, respectively). In general, median NPP and NEP are strongly correlated (R2=0.83) across all biomes and age classes, with the exception of the youngest temperate forests. Using the information gained from calculating the summary statistics for NPP and NEP, we calculated heterotrophic soil respiration (Rh) for each age class in each biome. The mean Rh was high in the youngest temperate age class (9.7 Mg C ha?1 yr?1) and declined with age, implying that forest ecosystem respiration peaks when forests are young, not old. With notable exceptions, carbon pool sizes increased with age in all biomes, including soil C. Age trends in C cycling and storage are very apparent in all three biomes and it is clear that a better understanding of how forest age and disturbance history interact will greatly improve our fundamental knowledge of the terrestrial C cycle.  相似文献   

15.
S. LUYSSAERT  I. INGLIMA  M. JUNG  A. D. RICHARDSON  M. REICHSTEIN  D. PAPALE  S. L. PIAO  E. ‐D. SCHULZE  L. WINGATE  G. MATTEUCCI  L. ARAGAO  M. AUBINET  C. BEER  C. BERNHOFER  K. G. BLACK  D. BONAL  J. ‐M. BONNEFOND  J. CHAMBERS  P. CIAIS  B. COOK  K. J. DAVIS  A. J. DOLMAN  B. GIELEN  M. GOULDEN  J. GRACE  A. GRANIER  A. GRELLE  T. GRIFFIS  T. GRÜNWALD  G. GUIDOLOTTI  P. J. HANSON  R. HARDING  D. Y. HOLLINGER  L. R. HUTYRA  P. KOLARI  B. KRUIJT  W. KUTSCH  F. LAGERGREN  T. LAURILA  B. E. LAW  G. LE MAIRE  A. LINDROTH  D. LOUSTAU  Y. MALHI  J. MATEUS  M. MIGLIAVACCA  L. MISSON  L. MONTAGNANI  J. MONCRIEFF  E. MOORS  J. W. MUNGER  E. NIKINMAA  S. V. OLLINGER  G. PITA  C. REBMANN  O. ROUPSARD  N. SAIGUSA  M. J. SANZ  G. SEUFERT  C. SIERRA  M. ‐L. SMITH  J. TANG  R. VALENTINI  T. VESALA  I. A. JANSSENS 《Global Change Biology》2007,13(12):2509-2537
Terrestrial ecosystems sequester 2.1 Pg of atmospheric carbon annually. A large amount of the terrestrial sink is realized by forests. However, considerable uncertainties remain regarding the fate of this carbon over both short and long timescales. Relevant data to address these uncertainties are being collected at many sites around the world, but syntheses of these data are still sparse. To facilitate future synthesis activities, we have assembled a comprehensive global database for forest ecosystems, which includes carbon budget variables (fluxes and stocks), ecosystem traits (e.g. leaf area index, age), as well as ancillary site information such as management regime, climate, and soil characteristics. This publicly available database can be used to quantify global, regional or biome‐specific carbon budgets; to re‐examine established relationships; to test emerging hypotheses about ecosystem functioning [e.g. a constant net ecosystem production (NEP) to gross primary production (GPP) ratio]; and as benchmarks for model evaluations. In this paper, we present the first analysis of this database. We discuss the climatic influences on GPP, net primary production (NPP) and NEP and present the CO2 balances for boreal, temperate, and tropical forest biomes based on micrometeorological, ecophysiological, and biometric flux and inventory estimates. Globally, GPP of forests benefited from higher temperatures and precipitation whereas NPP saturated above either a threshold of 1500 mm precipitation or a mean annual temperature of 10 °C. The global pattern in NEP was insensitive to climate and is hypothesized to be mainly determined by nonclimatic conditions such as successional stage, management, site history, and site disturbance. In all biomes, closing the CO2 balance required the introduction of substantial biome‐specific closure terms. Nonclosure was taken as an indication that respiratory processes, advection, and non‐CO2 carbon fluxes are not presently being adequately accounted for.  相似文献   

16.
Operational monitoring of global terrestrial gross primary production (GPP) and net primary production (NPP) is now underway using imagery from the satellite‐borne Moderate Resolution Imaging Spectroradiometer (MODIS) sensor. Evaluation of MODIS GPP and NPP products will require site‐level studies across a range of biomes, with close attention to numerous scaling issues that must be addressed to link ground measurements to the satellite‐based carbon flux estimates. Here, we report results of a study aimed at evaluating MODIS NPP/GPP products at six sites varying widely in climate, land use, and vegetation physiognomy. Comparisons were made for twenty‐five 1 km2 cells at each site, with 8‐day averages for GPP and an annual value for NPP. The validation data layers were made with a combination of ground measurements, relatively high resolution satellite data (Landsat Enhanced Thematic Mapper Plus at ~30 m resolution), and process‐based modeling. There was strong seasonality in the MODIS GPP at all sites, and mean NPP ranged from 80 g C m?2 yr?1 at an arctic tundra site to 550 g C m?2 yr?1 at a temperate deciduous forest site. There was not a consistent over‐ or underprediction of NPP across sites relative to the validation estimates. The closest agreements in NPP and GPP were at the temperate deciduous forest, arctic tundra, and boreal forest sites. There was moderate underestimation in the MODIS products at the agricultural field site, and strong overestimation at the desert grassland and at the dry coniferous forest sites. Analyses of specific inputs to the MODIS NPP/GPP algorithm – notably the fraction of photosynthetically active radiation absorbed by the vegetation canopy, the maximum light use efficiency (LUE), and the climate data – revealed the causes of the over‐ and underestimates. Suggestions for algorithm improvement include selectively altering values for maximum LUE (based on observations at eddy covariance flux towers) and parameters regulating autotrophic respiration.  相似文献   

17.
To assess the variation in distribution, extent, and NPP of global natural vegetation in response to climate change in the period 1911–2000 and to provide a feasible method for climate change research in regions where historical data is difficult to obtain. In this research, variations in spatiotemporal distributions of global potential natural vegetation (PNV) from 1911 to 2000 were analyzed with the comprehensive sequential classification system (CSCS) and net primary production (NPP) of different ecosystems was evaluated with the synthetic model to determine the effect of climate change on the terrestrial ecosystems. The results showed that consistently rising global temperature and altered precipitation patterns had exerted strong influence on spatiotemporal distribution and productivities of terrestrial ecosystems, especially in the mid/high latitudes. Ecosystems in temperate zones expanded and desert area decreased as a consequence of climate variations. The vegetation that decreased the most was cold desert (18.79%), while the maximum increase (10.31%) was recorded in savanna. Additionally, the area of tundra and alpine steppe reduced significantly (5.43%) and were forced northward due to significant ascending temperature in the northern hemisphere. The global terrestrial ecosystems productivities increased by 2.09%, most of which was attributed to savanna (6.04%), tropical forest (0.99%), and temperate forest (5.49%). Most NPP losses were found in cold desert (27.33%). NPP increases displayed a latitudinal distribution. The NPP of tropical zones amounted to more than a half of total NPP, with an estimated increase of 1.32%. The increase in northern temperate zone was the second highest with 3.55%. Global NPP showed a significant positive correlation with mean annual precipitation in comparison with mean annual temperature and biological temperature. In general, effects of climate change on terrestrial ecosystems were deep and profound in 1911–2000, especially in the latter half of the period.  相似文献   

18.
We investigated a palynological section from middle Miocene sediments at Eskihisar (south‐western Anatolia) to establish biogeographic links of the palynoflora and to infer the palaeoenvironment. Four algal palynomorphs, nine spore taxa, eight gymnosperms, three monocots and 67 dicot pollen types were encountered and investigated using the ‘single grain method’ that combines light microscopy and scanning electron microscopy. Two pollen zones reflect different phases of basin development. Zonal vegetation remained fairly stable across the section and reflects heterogeneous environments including broad‐leaved deciduous forest, subtropical forest and sclerophyllous and semi‐evergreen oak forest. Conifers were accessory elements in the broad‐leaved deciduous forest communities and replaced these at higher elevations. Some herbaceous taxa (Plumbaginaceae) indicate scattered occurrences of sandy and/or rocky soils. Biogeographic affinities are general Northern Hemisphere, North American and East Asian, as also suggested by the macrofossil record. Only two taxa provide potential biogeographic links with the African flora. This suggests that biome shifts of plant taxa between African subtropical/tropical biomes and Anatolian (western Eurasian) temperate forests and shrublands may have been rare in the middle Miocene.  相似文献   

19.
Biomization provides an objective and robust method of assigning pollen spectra to biomes so that pollen data can be mapped and compared directly with the output of biomgeographic models. We have tested the applicability of this procedure, originally developed for Europe, to assign modern surface samples from China to biomes. The procedure successfully delineated the major vegetation types of China. When the same procedure was applied to fossil pollen samples for 6000 years ago, the reconstructions showed systematic differences from present, consistent with previous interpretations of vegetation changes since the mid-Holocene. In eastern China, the forest zones were systematically shifted northwards, such that cool mixed forests displaced taiga in northeastern China, while broad-leaved evergreen forest extended c. 300 km and temperate deciduous forestc. 500–600 km beyond their present northern limits. In northwestern China, the area of desert and steppe vegetation was reduced compared to present. On the Tibetan Plateau, forest vegetation extended to higher elevations than today and the area of tundra was reduced. These shifts in biome distributions imply significant changes in climate since 6000 years ago that can be interpreted qualitatively as a response to orbital forcing and its secondary effects on the Asian monsoon.  相似文献   

20.
1. Physiological experiments have indicated that the lower CO2 levels of the last glaciation (200 μmol mol?1) probably reduced plant water-use efficiency (WUE) and that they combined with increased aridity and colder temperatures to alter vegetation structure and composition at the Last Glacial Maximum (LGM). 2. The effects of low CO2 on vegetation structure were investigated using BIOME3 simulations of leaf area index (LAI), and a two-by-two factorial experimental design (modern/LGM CO2, modern/LGM climate).3. Using BIOME3, and a combination of lowered CO2 and simulated LGM climate (from the NCAR-CCM1 model), results in the introduction of additional xeric vegetation types between open woodland and closed-canopy forest along a latitudinal gradient in eastern North America.4. The simulated LAI of LGM vegetation was 25–60% lower in many regions of central and eastern United States relative to modern climate, indicating that glacial vegetation was much more open than today.5. Comparison of factorial simulations show that low atmospheric CO2 has the potential to alter vegetation structure (LAI) to a greater extent than LGM climate.6. If the magnitude of LAI reductions simulated for glacial North America were global, then low atmospheric CO2 may have promoted atmospheric warming and increased aridity, through alteration of rates of water and heat exchange with the atmosphere.  相似文献   

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