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How do tree structure and old age affect growth potential of California redwoods?

Ecological monographs, 2015-05, Vol.85 (2), p.181-212

2015

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Emergent crowns and light-use complementarity lead to global maximum biomass and leaf area in Sequoia sempervirens forests

Forest ecology and management, 2016-09, Vol.375, p.279-308

2016

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Millennium-scale crossdating and inter-annual climate sensitivities of standing California redwoods

PloS one, 2014-07, Vol.9 (7), p.e102545-e102545

2014

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Pushing the limits to tree height: could foliar water storage compensate for hydraulic constraints in Sequoia sempervirens?

Functional ecology, 2014-10, Vol.28 (5), p.1087-1093

2014

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Biomass and growth potential of Eucalyptus regnans up to 100m tall

Forest ecology and management, 2015-07, Vol.348, p.78-91

2015

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Leaf acclimation to light availability supports rapid growth in tall Picea sitchensis trees

Tree physiology, 2017-10, Vol.37 (10), p.1352-1366

2017

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Crown dynamics and wood production of Douglas-fir trees in an old-growth forest

Forest ecology and management, 2017-01, Vol.384, p.157-168

2017

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Effects of tree height on branch hydraulics, leaf structure and gas exchange in California redwoods

Plant, cell and environment, 2009-07, Vol.32 (7), p.743-757

2009

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Increasing wood production through old age in tall trees

Forest ecology and management, 2010-02, Vol.259 (5), p.976-994

2010

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Phenotypic plasticity of leaves enhances water-stress tolerance and promotes hydraulic conductivity in a tall conifer

American journal of botany, 2016-05, Vol.103 (5), p.796-807

2016

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Trunk reiteration promotes epiphytes and water storage in an old-growth redwood forest canopy

Ecological monographs, 2007-08, Vol.77 (3), p.335-359

2007

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Hydrostatic constraints on morphological exploitation of light in tall Sequoia sempervirens trees

Oecologia, 2008-07, Vol.156 (4), p.751-763

2008

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Updated dendrochronology and axial variation of climatic sensitivity in Sequoiadendron giganteum

Trees (Berlin, West), 2024-08, Vol.38 (4), p.863-877

2024

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The limits to tree height

Nature, 2004-04, Vol.428 (6985), p.851-854

2004

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Within‐crown plasticity in leaf traits among the tallest conifers

American journal of botany, 2019-02, Vol.106 (2), p.174-186

2019

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Structure and dynamics of forests dominated by Sequoiadendron giganteum

Forest ecology and management, 2019-09, Vol.448, p.218-239

2019

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Tracheid buckling buys time, foliar water uptake pays it back: Coordination of leaf structure and function in tall redwood trees

Plant, cell and environment, 2022-09, Vol.45 (9), p.2607-2616

2022

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Arboreal histosols in old-growth redwood forest canopies, Northern California

Soil Science Society of America journal, 2006-03, Vol.70 (2), p.408-418

2006

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Separating effects of crown structure and competition for light on trunk growth of Sequoia sempervirens

Forest ecology and management, 2015-12, Vol.358, p.26-40

2015

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Epiphyte communities on redwood (Sequoia sempervirens) in northwestern California

The Bryologist, 2007-09, Vol.110 (3), p.420-452

2007

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Shoot dimorphism enables Sequoia sempervirens to separate requirements for foliar water uptake and photosynthesis

American journal of botany, 2022-04, Vol.109 (4), p.564-579

2022

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A response to: Limitations within "The Limits to Tree Height"

American journal of botany, 2009-02, Vol.96 (2), p.545-547

2009

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Disturbance and species composition drive canopy structure and distribution of large trees in Olympic rainforests, USA

Landscape ecology, 2020-05, Vol.35 (5), p.1107-1125

2020

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Crown Development of Coastal Pseudotsuga menziesii, Including a Conceptual Model for Tall Conifers [Erratum: 2008 Aug., v. 78, no. 3, p. 488]

Ecological monographs, 2008-05, Vol.78 (2), p.283-311

2008

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Growth maximization trumps maintenance of leaf conductance in the tallest angiosperm

Oecologia, 2015-02, Vol.177 (2), p.321-331

2015

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How do tree structure and old age affect growth potential of California redwoods?

Emergent crowns and light-use complementarity lead to global maximum biomass and leaf area in Sequoia sempervirens forests

Millennium-scale crossdating and inter-annual climate sensitivities of standing California redwoods

Pushing the limits to tree height: could foliar water storage compensate for hydraulic constraints in Sequoia sempervirens?

Biomass and growth potential of Eucalyptus regnans up to 100m tall

Leaf acclimation to light availability supports rapid growth in tall Picea sitchensis trees

Crown dynamics and wood production of Douglas-fir trees in an old-growth forest

Effects of tree height on branch hydraulics, leaf structure and gas exchange in California redwoods

Increasing wood production through old age in tall trees

Phenotypic plasticity of leaves enhances water-stress tolerance and promotes hydraulic conductivity in a tall conifer

Trunk reiteration promotes epiphytes and water storage in an old-growth redwood forest canopy

Hydrostatic constraints on morphological exploitation of light in tall Sequoia sempervirens trees

Updated dendrochronology and axial variation of climatic sensitivity in Sequoiadendron giganteum

The limits to tree height

Within‐crown plasticity in leaf traits among the tallest conifers

Structure and dynamics of forests dominated by Sequoiadendron giganteum

Tracheid buckling buys time, foliar water uptake pays it back: Coordination of leaf structure and function in tall redwood trees

Arboreal histosols in old-growth redwood forest canopies, Northern California

Separating effects of crown structure and competition for light on trunk growth of Sequoia sempervirens

Epiphyte communities on redwood (Sequoia sempervirens) in northwestern California

Shoot dimorphism enables Sequoia sempervirens to separate requirements for foliar water uptake and photosynthesis

A response to: Limitations within "The Limits to Tree Height"

Disturbance and species composition drive canopy structure and distribution of large trees in Olympic rainforests, USA

Crown Development of Coastal Pseudotsuga menziesii, Including a Conceptual Model for Tall Conifers [Erratum: 2008 Aug., v. 78, no. 3, p. 488]

Growth maximization trumps maintenance of leaf conductance in the tallest angiosperm

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