scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1365-2486.2007.01420.X |
P50 | author | Michael G Ryan | Q56486522 |
P2093 | author name string | CREIGHTON M. LITTON | |
JAMES W. RAICH | |||
P2860 | cites work | ??? | Q55842508 |
Plant genotypic diversity predicts community structure and governs an ecosystem process. | Q33254373 | ||
Aboveground sink strength in forests controls the allocation of carbon below ground and its [CO2]-induced enhancement | Q35539972 | ||
Belowground carbon cycling in a humid tropical forest decreases with fertilization | Q39022889 | ||
A global analysis of root distributions for terrestrial biomes | Q39097908 | ||
Temperature influences carbon accumulation in moist tropical forests | Q39378907 | ||
Modeling changes in red spruce carbon balance and allocation in response to interacting ozone and nutrient stresses | Q39585128 | ||
Periodic carbon flushing to roots of Quercus rubra saplings affects soil respiration and rhizosphere microbial biomass. | Q45952107 | ||
Global allocation rules for patterns of biomass partitioning in seed plants | Q46120049 | ||
Respiratory carbon losses and the carbon-use efficiency of a northern hardwood forest, 1999-2003. | Q47769153 | ||
Net primary production of forests: a constant fraction of gross primary production? | Q50716353 | ||
Foliage, fine-root, woody-tissue and stand respiration in Pinus radiata in relation to nitrogen status. | Q50738060 | ||
Belowground carbon allocation in unfertilized and fertilized red pine plantations in northern Wisconsin. | Q50738930 | ||
A simple method for estimating gross carbon budgets for vegetation in forest ecosystems. | Q50739238 | ||
Root biomass allocation in the world's upland forests. | Q52262176 | ||
Products, requirements and efficiency of biosynthesis: a quantitative approach. | Q53940424 | ||
Global response of terrestrial ecosystem structure and function to CO2and climate change: results from six dynamic global vegetation models | Q56030445 | ||
The carbon balance of tropical, temperate and boreal forests | Q56805906 | ||
Fine Roots vs. Needles: A Comparison of 13C and 15N Dynamics in a Ponderosa Pine Forest Soil | Q57020848 | ||
Large-scale forest girdling shows that current photosynthesis drives soil respiration | Q57037054 | ||
Coupling of canopy gas exchange with root and rhizosphere respiration in a semi-arid forest | Q57182513 | ||
Belowground carbon allocation in forests estimated from litterfall and IRGA-based soil respiration measurements | Q57263274 | ||
Biometric and eddy-covariance based estimates of annual carbon storage in five eastern North American deciduous forests | Q57263276 | ||
Volatile organic compound emissions in relation to plant carbon fixation and the terrestrial carbon budget | Q57399269 | ||
Tree damage, allometric relationships, and above-ground net primary production in central Amazon forest | Q58059297 | ||
Exposure to an enriched CO2 atmosphere alters carbon assimilation and allocation in a pine forest ecosystem | Q58076525 | ||
Carbon storage and fluxes in ponderosa pine forests at different developmental stages | Q58311212 | ||
Long-term isoprene flux measurements above a northern hardwood forest | Q58316658 | ||
Belowground and aboveground biomass in young postfire lodgepole pine forests of contrasting tree density | Q58381871 | ||
Total Belowground Carbon Allocation in a Fast-growing Eucalyptus Plantation Estimated Using a Carbon Balance Approach | Q58381877 | ||
P433 | issue | 10 | |
P921 | main subject | forest ecosystem | Q106498439 |
P6104 | maintained by WikiProject | WikiProject Ecology | Q10818384 |
P1104 | number of pages | 21 | |
P304 | page(s) | 2089-2109 | |
P577 | publication date | 2007-10-01 | |
P1433 | published in | Global Change Biology | Q1531580 |
P1476 | title | Carbon allocation in forest ecosystems | |
P478 | volume | 13 |
Q47460560 | A free-air system for long-term stable carbon isotope labeling of adult forest trees |
Q57231606 | A lifetime perspective of biomass allocation in Quercus pubescens trees in a dry, alpine valley |
Q58688890 | A mechanistic ecohydrological model to investigate complex interactions in cold and warm water-controlled environments: 2. Spatiotemporal analyses |
Q92710327 | A meta-analysis of 1,119 manipulative experiments on terrestrial carbon-cycling responses to global change |
Q34004715 | A primer for data assimilation with ecological models using Markov Chain Monte Carlo (MCMC). |
Q30316657 | A pyrosequencing insight into sprawling bacterial diversity and community dynamics in decaying deadwood logs of Fagus sylvatica and Picea abies |
Q56965375 | A trait-based ecosystem model suggests that long-term responsiveness to rising atmospheric CO2concentration is greater in slow-growing than fast-growing plants |
Q38239557 | A tree-ring perspective on the terrestrial carbon cycle. |
Q39546886 | A worldview of root traits: the influence of ancestry, growth form, climate and mycorrhizal association on the functional trait variation of fine-root tissues in seed plants. |
Q42362053 | Above and below ground carbohydrate allocation differs between ash (Fraxinus excelsior L.) and beech (Fagus sylvatica L.). |
Q34400500 | Above- and below-ground carbon stocks in an indigenous tree (Mytilaria laosensis) plantation chronosequence in subtropical China |
Q21128971 | Above- and below-ground net primary productivity across ten Amazonian forests on contrasting soils |
Q44818519 | Above-ground woody carbon sequestration measured from tree rings is coherent with net ecosystem productivity at five eddy-covariance sites |
Q35191068 | Aboveground tree growth varies with belowground carbon allocation in a tropical rainforest environment |
Q58388480 | Age-dependent forest carbon sink: Estimation via inverse modeling |
Q90834752 | Allocation of forest net primary production varies by forest age and air temperature |
Q30658383 | Allocation of gross primary production in forest ecosystems: allometric constraints and environmental responses |
Q39127228 | Allometric constraints on, and trade-offs in, belowground carbon allocation and their control of soil respiration across global forest ecosystems |
Q46171899 | Allometric growth and allocation in forests: a perspective from FLUXNET. |
Q57030096 | Analysis of Microbial Diversity and Greenhouse Gas Production of Decaying Pine Logs |
Q41357504 | Anthropogenic nitrogen deposition enhances carbon sequestration in boreal soils |
Q38366609 | Are above- and below-ground phenology in sync? |
Q33835024 | Associations between growth, wood anatomy, carbon isotope discrimination and mortality in a Quercus robur forest |
Q46440231 | Atmospheric CO2 mole fraction affects stand-scale carbon use efficiency of sunflower by stimulating respiration in light |
Q46475416 | Belowground carbon flux links biogeochemical cycles and resource-use efficiency at the global scale |
Q92365906 | Beyond Static Benchmarking: Using Experimental Manipulations to Evaluate Land Model Assumptions |
Q35069898 | Biomass partitioning and its relationship with the environmental factors at the alpine steppe in Northern Tibet |
Q56990621 | Biomass production efficiency controlled by management in temperate and boreal ecosystems |
Q57161032 | Carbon accumulation in European forests |
Q39123358 | Carbon allocation in a Bornean tropical rainforest without dry seasons |
Q58413453 | Carbon allocation in boreal black spruce forests across regions varying in soil temperature and precipitation |
Q38976504 | Carbon and water fluxes from ponderosa pine forests disturbed by wildfire and thinning |
Q46087136 | Carbon density and distribution of six Chinese temperate forests |
Q39279000 | Carbon dioxide emitted from live stems of tropical trees is several years old. |
Q38382593 | Carbon dynamics of mature and regrowth tropical forests derived from a pantropical database (TropForC-db). |
Q44251298 | Carbon use efficiency and storage in terrestrial ecosystems |
Q56334470 | Cascading community and ecosystem consequences of introduced coconut palms (Cocos nucifera) in tropical islands |
Q58312291 | Causes and implications of persistent atmospheric carbon dioxide biases in Earth System Models |
Q30885602 | Change in terrestrial ecosystem water-use efficiency over the last three decades |
Q46442885 | Changes in turnover rather than production regulate biomass of ectomycorrhizal fungal mycelium across a Pinus sylvestris chronosequence |
Q50042344 | Clearcutting alters decomposition processes and initiates complex restructuring of fungal communities in soil and tree roots. |
Q30993351 | Comparisons of allometric and climate-derived estimates of tree coarse root carbon stocks in forests of the United States |
Q36339298 | Contrasting effects of nitrogen addition on soil respiration in two Mediterranean ecosystems |
Q38786356 | Current and future carbon budget at Takayama site, Japan, evaluated by a regional climate model and a process-based terrestrial ecosystem model. |
Q61796009 | Decadal biomass increment in early secondary succession woody ecosystems is increased by CO enrichment |
Q58052723 | Discrimination in Tree Stems O2 Uptake and the Dole Effect |
Q58388605 | Diversity and competition influence tree allometric relationships - developing functions for mixed-species forests |
Q34936542 | Does elevated CO2 alter silica uptake in trees? |
Q38410214 | Drought predisposes piñon-juniper woodlands to insect attacks and mortality |
Q57201017 | Ecosystem respiration and net primary productivity after 8–10 years of experimental through-fall reduction in an eastern Amazon forest |
Q46268316 | Ecosystem responses to elevated CO2 governed by plant-soil interactions and the cost of nitrogen acquisition |
Q31132535 | Ectomycorrhizal fungal response to warming is linked to poor host performance at the boreal-temperate ecotone |
Q56556671 | Edaphic controls on ecosystem-level carbon allocation in two contrasting Amazon forests |
Q46331300 | Effect of Simulated Climate Warming on the Ectomycorrhizal Fungal Community of Boreal and Temperate Host Species Growing Near Their Shared Ecotonal Range Limits |
Q57536103 | Effects of crown architecture and stand structure on light absorption in mixed and monospecific Fagus sylvatica and Pinus sylvestris forests along a productivity and climate gradient through Europe |
Q58649025 | Effects of land-use type and nitrogen addition on nitrous oxide and carbon dioxide production potentials in Japanese Andosols |
Q96126809 | Effects of nitrogen deposition and litter layer management on soil CO2, N2O, and CH4 emissions in a subtropical pine forestland |
Q37463566 | Elevated CO2 effects on plant carbon, nitrogen, and water relations: six important lessons from FACE. |
Q31154553 | Emergent climate and CO2 sensitivities of net primary productivity in ecosystem models do not agree with empirical data in temperate forests of eastern North America. |
Q38791238 | Environmental control of carbon allocation matters for modelling forest growth. |
Q57867273 | Estimating Soil Respiration in a Subalpine Landscape Using Point, Terrain, Climate, and Greenness Data |
Q58121006 | Estimating belowground biomass and root/shoot ratio of Phillyrea latifolia L. in the Mediterranean forest landscapes |
Q56169035 | Evaluating aerosol direct radiative effects on global terrestrial ecosystem carbon dynamics from 2003 to 2010 |
Q57889469 | Evaluating the Community Land Model in a pine stand with shading manipulations and 13CO2 labeling |
Q31161531 | Evaluation of climate-related carbon turnover processes in global vegetation models for boreal and temperate forests |
Q56724589 | Evidence and implications of recent and projected climate change in Alaska's forest ecosystems |
Q30990387 | Experimental soil warming and cooling alters the partitioning of recent assimilates: evidence from a (14)C-labelling study at the alpine treeline |
Q91460765 | Favorable effect of mycorrhizae on biomass production efficiency exceeds their carbon cost in a fertilization experiment |
Q51182122 | Fertile forests produce biomass more efficiently. |
Q56501983 | Fine root turnover and litter production of Norway spruce in a long-term temperature and nutrient manipulation experiment |
Q58263666 | Fluxes of energy, water, and carbon dioxide from mountain ecosystems at Niwot Ridge, Colorado |
Q57519313 | Foliar nitrogen in relation to plant traits and reflectance properties of New Hampshire forests |
Q57020783 | ForCent model development and testing using the Enriched Background Isotope Study experiment |
Q39930563 | Forest annual carbon cost: a global-scale analysis of autotrophic respiration |
Q46206713 | Forest biomass, productivity and carbon cycling along a rainfall gradient in West Africa. |
Q100761856 | Forest production efficiency increases with growth temperature |
Q31053454 | Forest understory plant and soil microbial response to an experimentally induced drought and heat-pulse event: the importance of maintaining the continuum |
Q36119063 | From systems biology to photosynthesis and whole-plant physiology: a conceptual model for integrating multi-scale networks |
Q46796369 | Genetics of superior growth traits in trees are being mapped but will the faster-growing risk-takers make it in the wild? |
Q38931956 | Global patterns and predictors of stem CO2 efflux in forest ecosystems |
Q30939888 | Growth duration is a better predictor of stem increment than carbon supply in a Mediterranean oak forest: implications for assessing forest productivity under climate change. |
Q58261793 | High-latitude tree growth and satellite vegetation indices: Correlations and trends in Russia and Canada (1982–2008) |
Q60583303 | Hydrologic remediation for the Deepwater Horizon incident drove ancillary primary production increase in coastal swamps |
Q56334957 | Impact of nonnative feral pig removal on soil structure and nutrient availability in Hawaiian tropical montane wet forests |
Q39206954 | Impacts of individual tree species on carbon dynamics in a moist tropical forest environment |
Q38626446 | Improving predictions of tropical forest response to climate change through integration of field studies and ecosystem modeling. |
Q33792492 | In situ assessment of the velocity of carbon transfer by tracing 13 C in trunk CO2 efflux after pulse labelling: variations among tree species and seasons. |
Q59799542 | Increases in mean annual temperature do not alter soil bacterial community structure in tropical montane wet forests |
Q39785119 | Increases in the flux of carbon belowground stimulate nitrogen uptake and sustain the long-term enhancement of forest productivity under elevated CO₂. |
Q58049359 | Interannual variability of evapotranspiration and vegetation productivity |
Q44946081 | Is the growth of temperate forest trees enhanced along an ambient nitrogen deposition gradient? |
Q110951168 | Leaf hydraulics coordinated with leaf economics and leaf size in mangrove species along a salinity gradient |
Q58112802 | Long-term Wood Production in Water-Limited Forests: Evaluating Potential CO2 Fertilization Along with Historical Confounding Factors |
Q39333275 | Long-term dynamics of mycorrhizal root tips in a loblolly pine forest grown with free-air CO2 enrichment and soil N fertilization for 6 years |
Q57261951 | Magnani et al. reply |
Q100416590 | Mean annual temperature influences local fine root proliferation and arbuscular mycorrhizal colonization in a tropical wet forest |
Q34141260 | Modeling carbon allocation in trees: a search for principles |
Q45232761 | Modeling forest stand dynamics from optimal balances of carbon and nitrogen |
Q21132326 | Network analysis reveals ecological links between N-fixing bacteria and wood-decaying fungi |
Q30848008 | New insights into mechanisms driving carbon allocation in tropical forests |
Q58407973 | Nitrogen limitation in a sweetgum plantation: implications for carbon allocation and storage |
Q46909249 | Nitrogen-addition effects on leaf traits and photosynthetic carbon gain of boreal forest understory shrubs |
Q56990580 | Nutrient availability and climate as the main determinants of the ratio of biomass to NPP in woody and non-woody forest compartments |
Q56990806 | Nutrient availability as the key regulator of global forest carbon balance |
Q35390789 | Nutrient levels within leaves, stems, and roots of the xeric species Reaumuria soongorica in relation to geographical, climatic, and soil conditions |
Q46265024 | Nutrient-rich plants emit a less intense blend of volatile isoprenoids. |
Q56755223 | Optimal Function Explains Forest Responses to Global Change |
Q46240647 | Patterns in spatial distribution and root trait syndromes for ecto and arbuscular mycorrhizal temperate trees in a mixed broadleaf forest |
Q51149562 | Patterns of above- and belowground biomass allocation in China's grasslands: evidence from individual-level observations. |
Q58389528 | Photosynthetic capacity of Eucalyptus globulus is higher when grown in mixture with Acacia mearnsii |
Q39611738 | Plants adapted to nutrient limitation allocate less biomass into stems in an arid-hot grassland |
Q36410991 | Plasticity in gas-exchange physiology of mature Scots pine and European larch drive short- and long-term adjustments to changes in water availability |
Q30655875 | Predicting yields of short-rotation hybrid poplar (Populus spp.) for the United States through model-data synthesis |
Q34304733 | Pulse-labelling trees to study carbon allocation dynamics: a review of methods, current knowledge and future prospects |
Q30867179 | Rapid carbon turnover beneath shrub and tree vegetation is associated with low soil carbon stocks at a subarctic treeline |
Q39931699 | Re-assessment of plant carbon dynamics at the Duke free-air CO(2) enrichment site: interactions of atmospheric [CO(2)] with nitrogen and water availability over stand development |
Q28086775 | Redefining fine roots improves understanding of below-ground contributions to terrestrial biosphere processes |
Q56754981 | Redefinition and global estimation of basal ecosystem respiration rate |
Q31146634 | Reduced snow cover alters root-microbe interactions and decreases nitrification rates in a northern hardwood forest |
Q57044831 | Reduction of forest soil respiration in response to nitrogen deposition |
Q30829784 | Regional analysis of drought and heat impacts on forests: current and future science directions. |
Q56755164 | Relationships between net primary productivity and forest stand age in U.S. forests |
Q57581401 | Respiratory C fluxes and root exudation differ in two full-sib clones of Pinus taeda (L.) under contrasting fertilizer regimes in a greenhouse |
Q34249044 | Responses of bacterial and fungal communities to an elevation gradient in a subtropical montane forest of China |
Q41380027 | Responses of belowground carbon allocation dynamics to extended shading in mountain grassland |
Q33732065 | Scaling relationships of twig biomass allocation in Pinus hwangshanensis along an altitudinal gradient |
Q46551902 | Seasonal dynamics of δ(13) C of C-rich fractions from Picea abies (Norway spruce) and Fagus sylvatica (European beech) fine roots. |
Q57201025 | Seasonal production, allocation and cycling of carbon in two mid-elevation tropical montane forest plots in the Peruvian Andes |
Q58688879 | Sensitivity analysis of a process-based ecosystem model: Pinpointing parameterization and structural issues |
Q58690443 | Silver Fir Defoliation Likelihood Is Related to Negative Growth Trends and High Warming Sensitivity at Their Southernmost Distribution Limit |
Q38185627 | Simple additive effects are rare: a quantitative review of plant biomass and soil process responses to combined manipulations of CO2 and temperature |
Q28587496 | Simulated effects of nitrogen saturation on the global carbon budget using the IBIS model |
Q58380536 | Slowed Biogeochemical Cycling in Sub-arctic Birch Forest Linked to Reduced Mycorrhizal Growth and Community Change after a Defoliation Event |
Q41196520 | Slower phloem transport in gymnosperm trees can be attributed to higher sieve element resistance |
Q57432604 | Soil acidification exerts a greater control on soil respiration than soil nitrogen availability in grasslands subjected to long-term nitrogen enrichment |
Q37810310 | Sources of variability in canopy reflectance and the convergent properties of plants. |
Q56990846 | Spatial variability and controls over biomass stocks, carbon fluxes, and resource-use efficiencies across forest ecosystems |
Q21131092 | Specificity of plant-microbe interactions in the tree mycorrhizosphere biome and consequences for soil C cycling |
Q51183553 | Stand-level patterns of carbon fluxes and partitioning in a Eucalyptus grandis plantation across a gradient of productivity, in Sao Paulo State, Brazil. |
Q30581191 | Steeper declines in forest photosynthesis than respiration explain age-driven decreases in forest growth |
Q39404998 | Stem CO2 efflux in six co-occurring tree species: underlying factors and ecological implications |
Q31031707 | Stronger warming effects on microbial abundances in colder regions. |
Q99416281 | Surplus Carbon Drives Allocation and Plant-Soil Interactions |
Q57026323 | Surrounding species diversity improves subtropical seedlings' carbon dynamics |
Q51227168 | Sustained effects of atmospheric [CO2] and nitrogen availability on forest soil CO2 efflux. |
Q57196268 | Terrestrial ecosystem model performance in simulating productivity and its vulnerability to climate change in the northern permafrost region |
Q35768168 | The Oldest, Slowest Rainforests in the World? Massive Biomass and Slow Carbon Dynamics of Fitzroya cupressoides Temperate Forests in Southern Chile. |
Q43412610 | The influence of preparation method on measured carbon fractions in tree tissues |
Q59302418 | The production and turnover of extramatrical mycelium of ectomycorrhizal fungi in forest soils: role in carbon cycling |
Q56832479 | The production, storage, and flow of carbon in Amazonian forests |
Q50525818 | The role of canopy structural complexity in wood net primary production of a maturing northern deciduous forest. |
Q44861222 | The role of mosses in carbon uptake and partitioning in arctic vegetation |
Q58069164 | The role of vegetation in methane flux to the atmosphere: should vegetation be included as a distinct category in the global methane budget? |
Q56556839 | The seasonal cycle of productivity, metabolism and carbon dynamics in a wet aseasonal forest in north-west Amazonia (Iquitos, Peru) |
Q28484679 | The terrestrial silica pump |
Q58073522 | The value of soil respiration measurements for interpreting and modeling terrestrial carbon cycling |
Q39207956 | The variation of productivity and its allocation along a tropical elevation gradient: a whole carbon budget perspective |
Q58413399 | Thinning Can Reduce Losses in Carbon Use Efficiency and Carbon Stocks in Managed Forests Under Warmer Climate |
Q42499746 | Timing and magnitude of C partitioning through a young loblolly pine (Pinus taeda L.) stand using 13C labeling and shade treatments |
Q58653028 | Total belowground carbon flux in subalpine forests is related to leaf area index, soil nitrogen, and tree height |
Q57044886 | Toward a consistency cross-check of eddy covariance flux-based and biometric estimates of ecosystem carbon balance |
Q46847437 | Tree carbon allocation dynamics determined using a carbon mass balance approach. |
Q36393818 | Tree-ring analysis and modeling approaches yield contrary response of circumboreal forest productivity to climate change |
Q58390242 | Uncertainty Quantification of Extratropical Forest Biomass in CMIP5 Models over the Northern Hemisphere |
Q38881077 | Variation in foliar respiration and wood CO2 efflux rates among species and canopy layers in a wet tropical forest. |
Q51247946 | Vertical gradients and seasonal variation in stem CO2 efflux within a Norway spruce stand. |
Q39123351 | Vertical variations in wood CO2 efflux for live emergent trees in a Bornean tropical rainforest. |
Q37017667 | Viewing forests from below: fine root mass declines relative to leaf area in aging lodgepole pine stands |
Q58398657 | Water limitation to soil CO2efflux in a pine forest at the semiarid “timberline” |
Q41968881 | What controls plant nutrient use in high elevation ecosystems? |
Q30976606 | Where does the carbon go?--Plant carbon allocation under climate change. |
Q40261635 | Wood phenology, not carbon input, controls the interannual variability of wood growth in a temperate oak forest |
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