scholarly article | Q13442814 |
P819 | ADS bibcode | 2002Oecol.132...12M |
P356 | DOI | 10.1007/S00442-002-0904-X |
P698 | PubMed publication ID | 28547290 |
P5875 | ResearchGate publication ID | 225383628 |
P50 | author | Frederick C Meinzer | Q39051081 |
Michael G Ryan | Q56486522 | ||
Robert M Hubbard | Q56561015 | ||
P2093 | author name string | J Marshall | |
H Ishii | |||
D Whitehead | |||
N Phillips | |||
B Bond | |||
F Magnani | |||
H Barnard | |||
N McDowell | |||
B Köstner | |||
T Hinckley | |||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 9 | |
P304 | page(s) | 12-20 | |
P577 | publication date | 2002-06-01 | |
P1433 | published in | Oecologia | Q3349418 |
P1476 | title | The relationship between tree height and leaf area: sapwood area ratio | |
P478 | volume | 132 |
Q104928950 | A test of the hydraulic limitation hypothesis in fast-growing Eucalyptus saligna |
Q57029893 | Adjustments in hydraulic architecture of Pinus palustris maintain similar stomatal conductance in xeric and mesic habitats |
Q41974157 | Bud development and shoot morphology in relation to crown location |
Q46368932 | Canopy gradients in leaf functional traits for species that differ in growth strategies and shade tolerance |
Q38893771 | Climate-related trends in sapwood biophysical properties in two conifers: avoidance of hydraulic dysfunction through coordinated adjustments in xylem efficiency, safety and capacitance |
Q38764668 | Common allometric response of open-grown leader shoots to tree height in co-occurring deciduous broadleaved trees |
Q58395568 | Comparison of tree transpiration under wet and dry canopy conditions in a Costa Rican premontane tropical forest |
Q57160931 | Comprehensive ecosystem model-data synthesis using multiple data sets at two temperate forest free-air CO2enrichment experiments: Model performance at ambient CO2concentration |
Q58310700 | Convergence of tree water use and hydraulic architecture in water-limited regions: a review and synthesis |
Q58381793 | Converging patterns of vertical variability in leaf morphology and nitrogen across seven Eucalyptus plantations in Brazil and Hawaii, USA |
Q57889625 | Coupling carbon allocation with leaf and root phenology predicts tree–grass partitioning along a savanna rainfall gradient |
Q58384023 | Crown conductance in dwarf, medium, and tall pitch pines in the Long Island Pine Plains |
Q91155515 | Different ways to die in a changing world: Consequences of climate change for tree species performance and survival through an ecophysiological perspective |
Q57024212 | Drought, fire and tree survival in a Borneo rain forest, East Kalimantan, Indonesia |
Q39040858 | Ecophysiological variation of transpiration of pine forests: synthesis of new and published results |
Q57161067 | Effect Of Height On Tree Hydraulic Conductance Incompletely Compensated By Xylem Tapering |
Q57433769 | Effects of age-related increases in sapwood area, leaf area, and xylem conductivity on height-related hydraulic costs in two contrasting coniferous species |
Q80938699 | Effects of light availability versus hydraulic constraints on stomatal responses within a crown of silver birch |
Q58413461 | Effects of stand age and tree species on canopy transpiration and average stomatal conductance of boreal forests |
Q30992176 | Environmental sensitivity of gas exchange in different-sized trees |
Q39549326 | Explaining biomass growth of tropical canopy trees: the importance of sapwood |
Q112766965 | Foliar and Wood Traits Covary along a Vertical Gradient within the Crown of Long-Lived Light-Demanding Species of the Congo Basin Semi-Deciduous Forest |
Q46644895 | Functional ratios among leaf, xylem and phloem areas in branches change with shade tolerance, but not with local light conditions, across temperate tree species. |
Q47771055 | Giant eucalypts - globally unique fire-adapted rain-forest trees? |
Q57034310 | Growth and water relations of Tamarix ramosissima and Populus euphratica on Taklamakan desert dunes in relation to depth to a permanent water table |
Q46794305 | Growth maximization trumps maintenance of leaf conductance in the tallest angiosperm |
Q39115210 | Hawaiian native forest conserves water relative to timber plantation: species and stand traits influence water use. |
Q39233223 | Homeostatic maintenance of ponderosa pine gas exchange in response to stand density changes |
Q33355580 | Hormonal signals involved in the regulation of cambial activity, xylogenesis and vessel patterning in trees. |
Q51653023 | Hydraulic adjustment of Scots pine across Europe. |
Q51728442 | Hydraulic compensation in northern Rocky Mountain conifers: does successional position and life history matter? |
Q61796350 | Hydraulic traits are coordinated with maximum plant height at the global scale |
Q35779063 | Impacts of invading alien plant species on water flows at stand and catchment scales |
Q47294090 | Impacts of tree height on leaf hydraulic architecture and stomatal control in Douglas-fir |
Q57161061 | Implementing plant hydraulic architecture within the LPJ Dynamic Global Vegetation Model |
Q46821485 | Increases in atmospheric CO2 have little influence on transpiration of a temperate forest canopy |
Q58690386 | Influence of Tree Age and Variety on Allometric Characteristics and Water Use of Mangifera indica L. Growing in Plantation |
Q51318267 | Interplay of growth rate and xylem plasticity for optimal coordination of carbon and hydraulic economies in Fraxinus ornus trees. |
Q39159002 | Limited genetic variability and phenotypic plasticity detected for cavitation resistance in a Mediterranean pine |
Q40350150 | Long-term impact of Ophiostoma novo-ulmi on leaf traits and transpiration of branches in the Dutch elm hybrid 'Dodoens'. |
Q58763525 | Maintenance mechanisms of the pipe model relationship and Leonardo da Vinci’s rule in the branching architecture of Acer rufinerve trees |
Q60576740 | Modelling the impacts of the foliar pathogen, Phaeocryptopus gaeumannii, on Douglas-fir physiology: net canopy carbon assimilation, needle abscission and growth |
Q114018756 | Modelling the response of net primary productivity of the Zambezi teak forests to climate change along a rainfall gradient in Zambia |
Q35226368 | Morphological and moisture availability controls of the leaf area-to-sapwood area ratio: analysis of measurements on Australian trees |
Q57056461 | Oak powdery mildew changes growth patterns in its host tree: host tolerance response and potential manipulation of host physiology by the parasite |
Q58653538 | On the applicability of the pipe model theory on the chestnut tree (Castanea sativa Mill.) |
Q47267443 | Physiological and morphological acclimation to height in cupressoid leaves of 100-year-old Chamaecyparis obtusa |
Q57261962 | Plasticity in hydraulic architecture of Scots pine across Eurasia |
Q58382594 | Relating water use to morphology and environment of Nothofagus from the world’s most southern forests |
Q42845246 | Scaling of xylem and phloem transport capacity and resource usage with tree size. |
Q34077222 | Sensitivity of ring growth and carbon allocation to climatic variation vary within ponderosa pine trees |
Q58396298 | Stem xylem conductivity is key to plant water balance across Australian angiosperm species |
Q46930617 | Structural adjustments in resprouting trees drive differences in post-fire transpiration. |
Q58385874 | Tamarix transpiration along a semiarid river has negligible impact on water resources |
Q38698805 | The blind men and the elephant: the impact of context and scale in evaluating conflicts between plant hydraulic safety and efficiency |
Q47430780 | The challenge of tree height in Eucalyptus regnans: when xylem tapering overcomes hydraulic resistance. |
Q45834757 | The effects of elevated CO2 and nitrogen fertilization on stomatal conductance estimated from 11 years of scaled sap flux measurements at Duke FACE. |
Q36642368 | The hydraulic limitation hypothesis revisited |
Q50787964 | The importance of age-related decline in forest NPP for modeling regional carbon balances. |
Q36332364 | The importance of hydraulic architecture to the distribution patterns of trees in a central Amazonian forest |
Q47556428 | The pipe model theory half a century on: a review |
Q56755131 | Traits to stay, traits to move: a review of functional traits to assess sensitivity and adaptive capacity of temperate and boreal trees to climate change |
Q58318693 | Transpiration and stomatal conductance across a steep climate gradient in the southern Rocky Mountains |
Q58395546 | Transpiration in recovering mixed loblolly pine and oak stands following wildfire in the Lost Pines region of Texas |
Q36070951 | Tree Morphologic Plasticity Explains Deviation from Metabolic Scaling Theory in Semi-Arid Conifer Forests, Southwestern USA |
Q47321193 | Tree height and age-related decline in growth in Scots pine (Pinus sylvestris L.). |
Q38368131 | Tree height strongly affects estimates of water-use efficiency responses to climate and CO2 using isotopes. |
Q51102439 | Tsuga canadensis (L.) Carr. mortality will impact hydrologic processes in southern Appalachian forest ecosystems. |
Q91800717 | Using morphological attributes for the fast assessment of nutritional responses of Buddhist pine (Podocarpus macrophyllus [Thunb.] D. Don) seedlings to exponential fertilization |
Q27306858 | Why Be a Shrub? A Basic Model and Hypotheses for the Adaptive Values of a Common Growth Form |
Search more.