Biome-specific effects of nitrogen and phosphorus on the photosynthetic characteristics of trees at a forest-savanna boundary in Cameroon

[1]  D. Mueller‐Dombois,et al.  BOOK REVIEW By SJG Ecology of Tropical and Subtropical Vegetation , 2016 .

[2]  G. Farquhar,et al.  Contrasting photosynthetic characteristics of forest vs. savanna species (Far North Queensland, Australia) , 2014 .

[3]  Stephen Sitch,et al.  Analysing Amazonian forest productivity using a new individual and trait-based model (TFS v.1) , 2014 .

[4]  O. Phillips,et al.  Structural, physiognomic and above-ground biomass variation in savanna–forest transition zones on three continents – how different are co-occurring savanna and forest formations? , 2014 .

[5]  W. J. Lucas,et al.  Molecular mechanisms underlying phosphate sensing, signaling, and adaptation in plants. , 2014, Journal of integrative plant biology.

[6]  S. Lewis,et al.  Foliar trait contrasts between African forest and savanna trees: genetic versus environmental effects. , 2014, Functional plant biology : FPB.

[7]  R Core Team,et al.  R: A language and environment for statistical computing. , 2014 .

[8]  Y. Nouvellon,et al.  Photosynthetic and anatomical responses of Eucalyptus grandis leaves to potassium and sodium supply in a field experiment. , 2014, Plant, cell & environment.

[9]  R. Q. Thomas,et al.  Global patterns of nitrogen limitation: confronting two global biogeochemical models with observations , 2013, Global change biology.

[10]  G. Farquhar,et al.  Photosynthetically relevant foliar traits correlating better on a mass vs an area basis: of ecophysiological relevance or just a case of mathematical imperatives and statistical quicksand? , 2013, The New phytologist.

[11]  M. Lomas,et al.  Evaluation of terrestrial carbon cycle models for their response to climate variability and to CO2 trends , 2013, Global change biology.

[12]  S. Pacala,et al.  Global Leaf Trait Relationships: Mass, Area, and the Leaf Economics Spectrum , 2013, Science.

[13]  S. Patiño,et al.  Ecophysiology of Forest and Savanna Vegetation , 2013 .

[14]  Seasonal variation in leaf traits between congeneric savanna and forest trees in Central Brazil: implications for forest expansion into savanna , 2013, Trees.

[15]  O. Phillips,et al.  On the delineation of tropical vegetation types with an emphasis on forest/savanna transitions , 2013 .

[16]  I. Woodhouse,et al.  Measuring biomass changes due to woody encroachment and deforestation/degradation in a forest-savanna boundary region of central Africa using multi-temporal L-band radar backscatter , 2011 .

[17]  Benjamin L Turner,et al.  Proteaceae from severely phosphorus-impoverished soils extensively replace phospholipids with galactolipids and sulfolipids during leaf development to achieve a high photosynthetic phosphorus-use-efficiency. , 2012, The New phytologist.

[18]  Atul K. Jain,et al.  The distribution of soil phosphorus for global biogeochemical modeling , 2012 .

[19]  Daniel S. Goll,et al.  Nutrient limitation reduces land carbon uptake in simulations with a model of combined carbon, nitrogen and phosphorus cycling , 2012 .

[20]  J. Terborgh,et al.  Basin-wide variations in Amazon forest structure and function are mediated by both soils and climate , 2012 .

[21]  Nate G. McDowell,et al.  Toward a Mechanistic Modeling of Nitrogen Limitation on Vegetation Dynamics , 2012, PloS one.

[22]  C. Quesada,et al.  Deriving Plant Functional Types for Amazonian forests for use in vegetation dynamics models , 2012 .

[23]  Stephen Sitch,et al.  Variations in Amazon forest productivity correlated with foliar nutrients and modelled rates of photosynthetic carbon supply , 2011, Philosophical Transactions of the Royal Society B: Biological Sciences.

[24]  Michael R. Chernick,et al.  An Introduction to Bootstrap Methods with Applications to R , 2011 .

[25]  S. Higgins,et al.  When is a ‘forest’ a savanna, and why does it matter? , 2011 .

[26]  Benjamin L Turner,et al.  Responses of Legume Versus Nonlegume Tropical Tree Seedlings to Elevated CO2 Concentration1[OA] , 2011, Plant Physiology.

[27]  T. Feldpausch,et al.  Co-limitation of photosynthetic capacity by nitrogen and phosphorus in West Africa woodlands. , 2010, Plant, cell & environment.

[28]  A. Arneth,et al.  Variations in chemical and physical properties of Amazon forest soils in relation to their genesis , 2010 .

[29]  G. Goldstein,et al.  Allocation to leaf area and sapwood area affects water relations of co-occurring savanna and forest trees , 2010, Oecologia.

[30]  Yadvinder Malhi,et al.  Basin-wide variations in foliar properties of Amazonian forest: phylogeny, soils and climate. , 2009 .

[31]  Pete Smith,et al.  Integrating plant–soil interactions into global carbon cycle models , 2009 .

[32]  S. Saatchi,et al.  Measuring Woody Encroachment along a Forest–Savanna Boundary in Central Africa , 2009 .

[33]  S. Gotsch,et al.  Tree topkill, not mortality, governs the dynamics of savanna-forest boundaries under frequent fire in central Brazil. , 2009, Ecology.

[34]  L. Anderson,et al.  Soils of Amazonia with particular reference to the RAINFOR sites , 2009 .

[35]  Ian J. Wright,et al.  Leaf phosphorus influences the photosynthesis–nitrogen relation: a cross-biome analysis of 314 species , 2009, Oecologia.

[36]  Y. Malhi,et al.  Carbon cost of plant nitrogen acquisition: A mechanistic, globally applicable model of plant nitrogen uptake, retranslocation, and fixation , 2010 .

[37]  M. Andersson,et al.  Membrane phospholipids as a phosphate reserve: the dynamic nature of phospholipid-to-digalactosyl diacylglycerol exchange in higher plants. , 2008, Plant, cell & environment.

[38]  I. C. Prentice,et al.  Evaluation of the terrestrial carbon cycle, future plant geography and climate‐carbon cycle feedbacks using five Dynamic Global Vegetation Models (DGVMs) , 2008 .

[39]  S. Itch,et al.  Evaluation of the terrestrial carbon cycle, future plant geography and climate-carbon cycle feedbacks using five Dynamic Global Vegetation Models (DGVMs) , 2008 .

[40]  J. Marengo,et al.  Paleo-environmental change in Amazonian and African rainforest during the LGM , 2006 .

[41]  M. Westoby,et al.  Bivariate line‐fitting methods for allometry , 2006, Biological reviews of the Cambridge Philosophical Society.

[42]  J. L. Parra,et al.  Very high resolution interpolated climate surfaces for global land areas , 2005 .

[43]  W. Hoffmann,et al.  Specific leaf area explains differences in leaf traits between congeneric savanna and forest trees , 2005 .

[44]  P. Reich,et al.  Global patterns of plant leaf N and P in relation to temperature and latitude. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[45]  S. Fritz,et al.  A new land‐cover map of Africa for the year 2000 , 2004 .

[46]  J. R. Evans Photosynthesis and nitrogen relationships in leaves of C3 plants , 2004, Oecologia.

[47]  Carl J. Bernacchi,et al.  Improved temperature response functions for models of Rubisco‐limited photosynthesis , 2001 .

[48]  S. V. Caemmerer,et al.  Biochemical models of leaf photosynthesis. , 2000 .

[49]  Ülo Niinemets,et al.  Research review. Components of leaf dry mass per area – thickness and density – alter leaf photosynthetic capacity in reverse directions in woody plants , 1999 .

[50]  J. Lloyd,et al.  Comparative sensitivity of ‘Prior Lisbon’ lemon and ‘Valencia’ orange trees to foliar sodium and chloride concentrations , 1989 .

[51]  Thomas J. Givnish,et al.  On the economy of plant form and function. , 1988 .

[52]  Christopher B. Field,et al.  photosynthesis--nitrogen relationship in wild plants , 1986 .

[53]  F. White,et al.  The Vegetation of Africa: A Descriptive Memoir to Accompany the UNESCO/AETFAT/UNSO Vegetation Map of Africa , 1985 .

[54]  F. White The vegetation of Africa : a descriptive memoir to accompany the Unesco/AETFAT/UNSO vegetation map of Africa , 1985 .

[55]  D. Mueller‐Dombois,et al.  Ecology of Tropical and Subtropical Vegetation. , 1972 .

[56]  J. A. Fleming,et al.  AMERICAN GEOPHYSICAL UNION. , 1945, Science.