Access the full text.
Sign up today, get DeepDyve free for 14 days.
J. Aber, SV Ollinger, C.Anthony Federer, PB Reich, ML Goulden, DW Kicklighter, JM Melillo, R. Lathrop (1995)
Predicting the effects of climate change on water yield and forest production in the northeastern United StatesClimate Research, 5
P. Reich, M. Walters, D. Ellsworth (1991)
Leaf age and season influence the relationships between leaf nitrogen, leaf mass per area and photosynthesis in maple and oak treesPlant Cell and Environment, 14
D. Sprugel (1989)
The Relationship of Evergreenness, Crown Architecture, and Leaf SizeThe American Naturalist, 133
P. Reich, M. Walters, D. Ellsworth (1992)
Leaf Life‐Span in Relation to Leaf, Plant, and Stand Characteristics among Diverse EcosystemsEcological Monographs, 62
C. Field, H. Mooney (1986)
photosynthesis--nitrogen relationship in wild plants
P. Vitousek, C. Field, P. Matson (1990)
Variation in foliar δ13C in Hawaiian Metrosideros polymorpha: a case of internal resistance?Oecologia, 84
S. Gower, Yowhan Son (1992)
Differences in Soil and Leaf Litterfall Nitrogen Dynamics for Five Forest PlantationsSoil Science Society of America Journal, 56
P. Reich, A. Schoettle (1988)
Role of phosphorus and nitrogen in photosynthetic and whole plant carbon gain and nutrient use efficiency in eastern white pineOecologia, 77
S. Gower, P. Reich, Yowhan Son (1993)
Canopy dynamics and aboveground production of five tree species with different leaf longevities.Tree physiology, 12 4
M. Walters, Christopher Field (1987)
Photosynthetic light acclimation in two rainforest Piper species with different ecological amplitudesOecologia, 72
P. Reich, D. Ellsworth, Brian Kloeppel, J. Fownes, S. Gower (1990)
Vertical variation in canopy structure and CO(2) exchange of oak-maple forests: influence of ozone, nitrogen, and other factors on simulated canopy carbon gain.Tree physiology, 7 1_2_3_4
P. Reich (1993)
Reconciling apparent discrepancies among studies relating life span, structure and function of leaves in contrasting plant life forms and climates: the blind men and the elephant retold'Functional Ecology, 7
J. Aber, Ollinger Sv, Lathrop Rg, F. Ca, Reich Pb, M. Goulden, Kicklighter Dw, Melillo Jm (1995)
Predicting the Effects of Climate Change on Water Yield and Forest Production in Northeastern U.S
E. DeLucia, T. Day, T. Vogelman (1992)
Ultraviolet‐B and visible light penetration into needles of two species of subalpine conifers during foliar developmentPlant Cell and Environment, 15
(1994)
JMP statistics and graphics guide , version 3
J. Evans (2004)
Photosynthesis and nitrogen relationships in leaves of C3 plantsOecologia, 78
F. Chapin (1980)
The Mineral Nutrition of Wild PlantsAnnual Review of Ecology, Evolution, and Systematics, 11
J. Aber, P. Reich, M. Goulden (1996)
Extrapolating leaf CO2 exchange to the canopy: a generalized model of forest photosynthesis compared with measurements by eddy correlationOecologia, 106
J. Lloyd, J. Syvertsen, P. Kriedemann, G. Farquhar (1992)
Low conductances for CO2 diffusion from stomata to the sites of carboxylation in leaves of woody speciesPlant Cell and Environment, 15
K. Kikuzawa (1991)
A Cost-Benefit Analysis of Leaf Habit and Leaf Longevity of Trees and Their Geographical PatternThe American Naturalist, 138
J. Pastor, J. Aber, C. Mcclaugherty, J. Melillo (1984)
Aboveground Production and N and P Cycling Along a Nitrogen Mineralization Gradient on Blackhawk Island, WisconsinEcology, 65
P. Reich, M. Walters, D. Ellsworth, C. Uhl (1994)
Photosynthesis-nitrogen relations in Amazonian tree speciesOecologia, 97
K. Williams, C. Field, H. Mooney (1989)
Relationships Among Leaf Construction Cost, Leaf Longevity, and Light Environment in Rain-Forest Plants of the Genus PiperThe American Naturalist, 133
(1993)
Spatial patterns of litterfall, nitrogen cycling and understory vegetation in a hemlock-hardwood forest
P. Reich, Christopher Uhl, M. Walters, D. Ellsworth (1991)
Leaf lifespan as a determinant of leaf structure and function among 23 amazonian tree speciesOecologia, 86
D. Ellsworth, P. Reich (1993)
Canopy structure and vertical patterns of photosynthesis and related leaf traits in a deciduous forestOecologia, 96
R. Chazdon, C. Field (1987)
Determinants of photosynthetic capacity in six rainforest Piper speciesOecologia, 73
The relationship between photosynthetic capacity ( A max ) and leaf nitrogen concentration ( N ) among all C 3 species can be described roughly with one general equation, yet within that overall pattern species groups or individual species may have markedly different A max - N relationships. To determine whether one or several predictive, fundamental A max - N relationships exist for temperate trees we measured A max , specific leaf area (SLA) and N in 22 broad-leaved deciduous and 9 needle-leaved evergreen tree species in Wisconsin, United States. For broad-leaved deciduous trees, mass-based A max was highly correlated with leaf N ( r 2 =0.75, P <0.001). For evergreen conifers, mass-based A max was also correlated with leaf N ( r 2 =0.59, P <0.001) and the slope of the regression (rate of increase of A max per unit increase in N ) was lower ( P <0.001) by two-thirds than in the broad-leaved species (1.9 vs. 6.4 μmol CO 2 g −1 N s −1 ), consistent with predictions based on tropical rain forest trees of short vs. long leaf life-span. On an area basis, there was a strong A max - N correlation among deciduous species ( r 2 =0.78, P <0.001) and no correlation ( r 2 =0.03, P >0.25) in the evergreen conifers. Compared to deciduous trees at a common leaf N (mass or area basis), evergreen trees had lower A max and SLA. For all data pooled, both leaf N and A max on a mass basis were correlated ( r 2 =0.6) with SLA; in contrast, area-based leaf N scaled tightly with SLA ( r 2 =0.81), but area-based A max did not ( r 2 =0.06) because of low A max per unit N in the evergreen conifers. Multiple regression analysis of all data pooled showed that both N (mass or area basis) and SLA were significantly ( P <0.001) related to A max on mass ( r 2 =0.80) and area ( r 2 =0.55) bases, respectively. These results provide further evidence that A max - N relationships are fundamentally different for ecologically distinct species groups with differing suites of foliage characteristics: species with long leaf life-spans and low SLA, whether broad-leaved or needle-leaved, tend to have lower A max per unit leaf N and a lower slope and higher intercept of the A max - N relation than do species with shorter leaf life-span and higher SLA. A single global A max - N equation overestimates and underestimates A max for temperate trees at the upper and lower end of their leaf N range, respectively. Users of A max - N relationships in modeling photosynthesis in different ecosystems should appreciate the strengths and limitations of regression equations based on different species groupings.
Oecologia – Springer Journals
Published: Sep 1, 1995
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.