human | Q5 |
P496 | ORCID iD | 0000-0001-7559-6572 |
P735 | given name | Frank | Q220546 |
Frank | Q220546 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q112772649 | 3-D GROWTH PATTERNS OF TREES: EFFECTS OF CARBON ECONOMY, MERISTEM ACTIVITY, AND SELECTION |
Q112768003 | A Conceptual Tree Model Explaining Legacy Effects on Stem Growth |
Q57231606 | A lifetime perspective of biomass allocation in Quercus pubescens trees in a dry, alpine valley |
Q36167614 | A synthesis of radial growth patterns preceding tree mortality |
Q115409068 | A trade‐off between growth and hydraulic resilience against freezing leads to divergent adaptations among temperate tree species |
Q62557023 | ARCHITECTURE OF 53 RAIN FOREST TREE SPECIES DIFFERING IN ADULT STATURE AND SHADE TOLERANCE |
Q122272772 | Abiotic and biotic drivers of liana community change in an Asian tropical rainforest |
Q39157532 | Allometric Trajectories and "Stress": A Quantitative Approach. |
Q36068564 | Allometric equations for integrating remote sensing imagery into forest monitoring programmes. |
Q115418016 | Arbuscular mycorrhiza and water and nutrient supply differently impact seedling performance of dry woodland species with different acquisition strategies |
Q36098988 | Arbuscular mycorrhizal fungi enhance photosynthesis, water use efficiency, and growth of frankincense seedlings under pulsed water availability conditions |
Q112804255 | Are leaf, stem and hydraulic traits good predictors of individual tree growth? |
Q57140074 | BAAD: a Biomass And Allometry Database for woody plants |
Q56784159 | Beyond the regeneration phase: differentiation of height-light trajectories among tropical tree species |
Q57577466 | Biomass partitioning and root morphology of savanna trees across a water gradient |
Q121009279 | Climate change induced elevational range shifts of Himalayan tree species |
Q110676385 | Combining dendrochronology and matrix modelling in demographic studies: An evaluation for Juniperus procera in Ethiopia |
Q92903421 | Conifer and broadleaved trees differ in branch allometry but maintain similar functional balances |
Q31046287 | Conservation of the Ethiopian church forests: Threats, opportunities and implications for their management |
Q115035212 | Considering inner and outer bark as distinctive tissues helps to disentangle the effects of bark traits on decomposition |
Q28710128 | Controls on coarse wood decay in temperate tree species: birth of the LOGLIFE experiment |
Q35804662 | Convergent Evolution towards High Net Carbon Gain Efficiency Contributes to the Shade Tolerance of Palms (Arecaceae). |
Q91454366 | Convergent xylem widening among organs across diverse woody seedlings |
Q112810565 | Crown development in tropical rain forest trees: patterns with tree height and light availability |
Q111367670 | Dead wood diversity promotes fungal diversity |
Q43082494 | Deciduous and evergreen trees differ in juvenile biomass allometries because of differences in allocation to root storage |
Q57577450 | Defence against vertebrate herbivores trades off into architectural and low nutrient strategies amongst savanna Fabaceae species |
Q91660636 | Determinants of legacy effects in pine trees - implications from an irrigation-stop experiment |
Q123217871 | Diel and seasonal stem growth responses to climatic variation are consistent across species in a subtropical tree community |
Q38441610 | Diel growth dynamics in tree stems: linking anatomy and ecophysiology |
Q100746158 | Differential determinants of growth rates in subtropical evergreen and deciduous juvenile trees: Carbon gain, hydraulics and nutrient use efficiencies |
Q52570890 | Divergent hydraulic strategies to cope with freezing in co-occurring temperate tree species with special reference to root and stem pressure generation. |
Q115447991 | Diversity and production of Ethiopian dry woodlands explained by climate- and soil-stress gradients |
Q58107802 | Does phloem osmolality affect diurnal diameter changes of twigs but not of stems in Scots pine? |
Q113708288 | Drought resilience of conifer species is driven by leaf lifespan but not by hydraulic traits |
Q125480096 | Drought- and heat-induced mortality of conifer trees is explained by leaf and growth legacies |
Q62549429 | Effective height development of four co-occurring species in the gap-phase regeneration of Douglas fir monocultures under nature-oriented conversion |
Q89088561 | Effects of bud-flushing strategies on tree growth |
Q51147679 | Effects of bud-flushing strategies on tree growth. |
Q39549326 | Explaining biomass growth of tropical canopy trees: the importance of sapwood |
Q59599546 | Faunal community consequence of interspecific bark trait dissimilarity in early-stage decomposing logs |
Q59516853 | Fine-root trait plasticity of beech (Fagus sylvatica) and spruce (Picea abies) forests on two contrasting soils |
Q112823650 | Frankincense tapping reduced photosynthetic carbon gain in Boswellia papyrifera (Burseraceae) trees |
Q39302012 | Frankincense tapping reduces the carbohydrate storage of Boswellia trees |
Q92843564 | Fully exposed canopy tree and liana branches in a tropical forest differ in mechanical traits but are similar in hydraulic traits |
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. |
Q34079985 | Functional traits determine trade-offs and niches in a tropical forest community |
Q112802793 | Functional traits shape tree species distribution in the Himalayas |
Q112651332 | Growth of 19 conifer species is highly sensitive to winter warming, spring frost and summer drought |
Q113175271 | Growth resilience of conifer species decreases with early, long‐lasting and intense droughts but cannot be explained by hydraulic traits |
Q112830126 | Height-diameter allometric relationships for seedlings and trees across China |
Q113708757 | Herbivory in Two Rain Forest Canopies in French Guyana |
Q112766730 | How do Light and Water Acquisition Strategies Affect Species Selection during Secondary Succession in Moist Tropical Forests? |
Q112820070 | How do lianas and trees change their vascular strategy in seasonal versus rain forest? |
Q30828445 | How light competition between plants affects their response to climate change |
Q112800682 | Hydraulic prediction of drought‐induced plant dieback and top‐kill depends on leaf habit and growth form |
Q115031792 | Incorporating belowground traits: avenues towards a whole‐tree perspective on performance |
Q60545145 | Inter-specific competition in mixed forests of Douglas-fir (Pseudotsuga menziesii) and common beech (Fagus sylvatica) under climate change — a model-based analysis |
Q59599535 | Is there a tree economics spectrum of decomposability? |
Q57577464 | Leaf adaptations of evergreen and deciduous trees of semi-arid and humid savannas on three continents |
Q39244984 | Leaf gas exchange in the frankincense tree (Boswellia papyrifera) of African dry woodlands |
Q112804500 | Lianas explore the forest canopy more effectively than trees under drier conditions |
Q112802864 | Lianas have more acquisitive traits than trees in a dry but not in a wet forest |
Q56769489 | Light fluctuations, crown traits, and response delays for tree saplings in a Costa Rican lowland rain forest |
Q39093030 | Linking size-dependent growth and mortality with architectural traits across 145 co-occurring tropical tree species |
Q112816009 | Long-term growth patterns of juvenile trees from a Bolivian tropical moist forest: shifting investments in diameter growth and height growth |
Q93012226 | Low growth resilience to drought is related to future mortality risk in trees |
Q92520311 | Magnetic resonance imaging suggests functional role of previous year vessels and fibres in ring-porous sap flow resumption |
Q62557019 | Mechanical branch constraints contribute to life-history variation across tree species in a Bolivian forest |
Q47357109 | Modelling functional trait acclimation for trees of different height in a forest light gradient: emergent patterns driven by carbon gain maximization |
Q46661573 | Non-structural carbohydrates in woody plants compared among laboratories |
Q112800658 | Number of growth days and not length of the growth period determines radial stem growth of temperate trees |
Q112818620 | Optimizing stand density for climate-smart forestry: A way forward towards resilient forests with enhanced carbon storage under extreme climate events |
Q36055155 | Osmolality and Non-Structural Carbohydrate Composition in the Secondary Phloem of Trees across a Latitudinal Gradient in Europe |
Q39489971 | Persisting soil drought reduces leaf specific conductivity in Scots pine (Pinus sylvestris) and pubescent oak (Quercus pubescens). |
Q39117338 | Pine and mistletoes: how to live with a leak in the water flow and storage system? |
Q111231770 | Pit and tracheid anatomy explain hydraulic safety but not hydraulic efficiency of 28 conifer species |
Q57051818 | Plasticity influencing the light compensation point offsets the specialization for light niches across shrub species in a tropical forest understorey |
Q115531935 | Postdispersal seed predation and seed viability in forest soils: implications for the regeneration of tree species in Ethiopian church forests |
Q36470639 | Resin secretory structures of Boswellia papyrifera and implications for frankincense yield. |
Q96113672 | Sapwood allocation in tropical trees: a test of hypotheses |
Q90424050 | Scots pine trees react to drought by increasing xylem and phloem conductivities |
Q59842519 | Seedling growth of savanna tree species from three continents under grass competition and nutrient limitation in a greenhouse experiment |
Q58383996 | Self-thinning in four pine species: an evaluation of potential climate impacts |
Q62549462 | Soil and light effects on the sapling performance of the shade-tolerant species Brosimum alicastrum (Moraceae) in a Mexican tropical rain forest |
Q112795775 | Soil nutrients, canopy gaps and topography affect liana distribution in a tropical seasonal rain forest in southwestern China |
Q60545121 | Species Mixing Effects on Forest Productivity: A Case Study at Stand-, Species- and Tree-Level in the Netherlands |
Q36352918 | Species distribution models predict temporal but not spatial variation in forest growth |
Q112767509 | Stem Trait Spectra Underpin Multiple Functions of Temperate Tree Species |
Q111231692 | Stem traits, compartments and tree species affect fungal communities on decaying wood |
Q31112092 | Stomatal regulation by microclimate and tree water relations: interpreting ecophysiological field data with a hydraulic plant model |
Q60545142 | Stress-Driven Changes in the Strength of Facilitation on Tree Seedling Establishment in West African Woodlands |
Q60866744 | Summer droughts limit tree growth across 10 temperate species on a productive forest site |
Q92348862 | TRY plant trait database - enhanced coverage and open access |
Q112632891 | Tallo–a global tree allometry and crown architecture database |
Q111231735 | Temperature and soils predict the distribution of plant species along the Himalayan elevational gradient |
Q34089616 | Terrestrial vs aquatic plants: how general is the drag tolerance-avoidance trade-off? |
Q113101889 | The frankincense tree Boswellia neglecta reveals high potential for restoration of woodlands in the Horn of Africa |
Q39363761 | The importance of wood traits and hydraulic conductance for the performance and life history strategies of 42 rainforest tree species |
Q112804628 | The role of fine‐root mass, specific root length and life span in tree performance: A whole‐tree exploration |
Q38833408 | Towards a multidimensional root trait framework: a tree root review |
Q115035315 | Towards effectively restoring agricultural landscapes in East African drylands: Linking plant functional traits with soil hydrology |
Q42174530 | Tradeoff between Stem Hydraulic Efficiency and Mechanical Strength Affects Leaf-Stem Allometry in 28 Ficus Tree Species |
Q31104220 | Trait Acclimation Mitigates Mortality Risks of Tropical Canopy Trees under Global Warming |
Q112272977 | Traits, strategies, and niches of liana species in a tropical seasonal rainforest |
Q62557008 | Tree architecture and life-history strategies across 200 co-occurring tropical tree species |
Q52588492 | Tree differences in primary and secondary growth drive convergent scaling in leaf area to sapwood area across Europe. |
Q35550100 | Tree growth variation in the tropical forest: understanding effects of temperature, rainfall and CO2. |
Q39139424 | Trees maintain a similar conductance per leaf area through integrated responses in growth, allocation, architecture and anatomy. |
Q30652103 | Tropical forests and global change: filling knowledge gaps. |
Q57231607 | Understanding trait interactions and their impacts on growth in Scots pine branches across Europe |
Q39374798 | Water-use strategies of six co-existing Mediterranean woody species during a summer drought |
Q62557001 | Wood density explains architectural differentiation across 145 co-occurring tropical tree species |
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