Pinus taeda clones and soil nutrient availability: effects of soil organic matter incorporation and fertilization on biomass partitioning and leaf physiology.

The combined effects of intensive management and planting of improved seedlings have led to large increases in productivity on intensively managed pine forests in the southeastern United States. To best match clones to particular site conditions, an understanding of how specific clones respond to changes in nutrition in terms of biomass partitioning, leaf physiology and biochemistry will be necessary. This study measured the response of biomass partitioning, light-saturated net photosynthesis (A(Sat)) and photosynthetic capacity to a range in soil fertility and fertilization between two contrasting Pinus taeda L. clone ideotypes: a 'narrow crown' clone (NC) that allocates more resources to stem growth and a 'broad crown' clone (BC) that allocates more resources to leaf area (LA). Under field conditions, we found consistent clone by environment (i.e., varying nutrient regimes) interactions in biomass as well as leaf physiology. Nutrient limitations induced by logging residue incorporation resulted in a 25% loss in stem growth in BC, while NC showed no response. We postulated that the decrease in BC was due to the differences in canopy architecture leading to a reduced canopy CO(2) assimilation, as well as to increased belowground maintenance costs associated with fine-root production. In contrast, N and P additions resulted in a 21% greater increase in stem volume in NC relative to BC. Fertilization increased A(Sat) temporarily in both clones, but A(Sat) eventually decreased below control levels by the end of the study. Although we found a clone by fertilization interaction in leaf physiology, the greatest genotype by environment interaction was found in the LA that appeared to have a greater influence than A(Sat) on growth. This research demonstrates the potential importance of selecting appropriate clonal material and silvicultural prescription when implementing site-specific silviculture to maximize productivity in intensively managed southern pine forests.

[1]  J. Seiler,et al.  Short-term impacts of nutrient manipulations on leaf gas exchange and biomass partitioning in contrasting 2-year-old Pinus taeda clones during seedling establishment , 2009 .

[2]  M. Tyree Genetics by Nutrient Availability Interactions on Short-term Carbon Pools and Fluxes in Young Pinus taeda Plantations , 2008 .

[3]  K. Johnsen,et al.  Genomic and physiological approaches to advancing forest tree improvement. , 2008, Tree physiology.

[4]  J. Seiler,et al.  Post-fertilization physiology and growth performance of loblolly pine clones. , 2008, Tree physiology.

[5]  M. Tjoelker,et al.  Leaf traits in relation to crown development, light interception and growth of elite families of loblolly and slash pine. , 2008, Tree physiology.

[6]  J. Tisdale Quantifying the effects of organic residues on soil nitrogen and phosphorus availability , 2008 .

[7]  Sari Palmroth,et al.  Short-term effects of fertilization on photosynthesis and leaf morphology of field-grown loblolly pine following long-term exposure to elevated CO2 concentration , 2008 .

[8]  T. Sharkey,et al.  Fitting photosynthetic carbon dioxide response curves for C(3) leaves. , 2007, Plant, cell & environment.

[9]  B. Richardson,et al.  Partititioning concurrent influences of nitrogen and phosphorus supply on photosynthetic model parameters of Pinus radiata. , 2007, Tree physiology.

[10]  H. Lee Allen,et al.  Tree Nutrition and Forest Fertilization of Pine Plantations in the Southern United States , 2007 .

[11]  Timothy A. Martin,et al.  Genotype × environment interactions in selected loblolly and slash pine plantations in the Southeastern United States , 2007 .

[12]  H. L. Allen,et al.  Performance of improved genotypes of loblolly pine across different soils, climates, and silvicultural inputs , 2006 .

[13]  E. Kruger,et al.  Reexamining the empirical relation between plant growth and leaf photosynthesis. , 2006, Functional plant biology : FPB.

[14]  T. Green,et al.  Effects of nitrogen on the response of loblolly pine to water stress I. Photosynthesis and stomatal conductance , 2006 .

[15]  D. Manter,et al.  Growth response of Douglas-fir seedlings to nitrogen fertilization: importance of Rubisco activation state and respiration rates. , 2005, Tree physiology.

[16]  H. Lee Allen,et al.  What is Ahead for Intensive Pine Plantation Silviculture in the South , 2005 .

[17]  R. Will The effects of annual fertilization and complete competition control on fascicle morphology of different aged loblolly pine stands , 2005, Trees.

[18]  Christopher M. Gough,et al.  Short‐term effects of fertilization on loblolly pine (Pinus taeda L.) physiology , 2004 .

[19]  C. Warren,et al.  Photosynthetic responses and N allocation in Douglas-fir needles following a brief pulse of nutrients. , 2004, Tree physiology.

[20]  M. Adams,et al.  Evergreen trees do not maximize instantaneous photosynthesis. , 2004, Trends in plant science.

[21]  Alexander Clark,et al.  Effect of complete competition control and annual fertilization on stem growth and canopy relations for a chronosequence of loblolly pine plantations in the lower coastal plain of Georgia , 2004 .

[22]  J. Roberds,et al.  Variation among slash pine families in chlorophyll fluorescence traits , 2003 .

[23]  R. Will,et al.  Effects of competition control and annual nitrogen fertilization on gas exchange of different-aged Pinus taeda , 2003 .

[24]  M. Adams,et al.  Photosynthesis-Rubisco relationships in foliage of Pinus sylvestris in response to nitrogen supply and the proposed role of Rubisco and amino acids as nitrogen stores , 2003, Trees.

[25]  G. Grassi,et al.  Photosynthesis-nitrogen relationships: interpretation of different patterns between Pseudotsuga menziesii and Populus x euroamericana in a mini-stand experiment. , 2003, Tree physiology.

[26]  K. Johnsen,et al.  Branch growth and gas exchange in 13-year-old loblolly pine (Pinus taeda) trees in response to elevated carbon dioxide concentration and fertilization. , 2002, Tree physiology.

[27]  Antonio Donato Nobre,et al.  Acclimation of photosynthetic capacity to irradiance in tree canopies in relation to leaf nitrogen concentration and leaf mass per unit area , 2002 .

[28]  R. Will,et al.  Relationship between intercepted radiation, net photosynthesis, respiration, and rate of stem volume growth of Pinus taeda and Pinus elliottii stands of different densities , 2001 .

[29]  W. Retzlaff,et al.  Whole-tree biomass and carbon allocation of juvenile trees of loblolly pine (Pinus taeda): influence of genetics and fertilization , 2001 .

[30]  Thomas R. Fox,et al.  Sustained productivity in intensively managed forest plantations , 2000 .

[31]  R. E. Dickson,et al.  Contrasting fine-root production, survival and soil CO2 efflux in pine and poplar plantations , 2000, Plant and Soil.

[32]  Allen,et al.  Stand-level allometry in Pinus taeda as affected by irrigation and fertilization. , 1999, Tree physiology.

[33]  Veronica C. Lessard,et al.  Variation in sugar maple root respiration with root diameter and soil depth. , 1998, Tree physiology.

[34]  H. L. Allen,et al.  Leaf Area and Above- and Belowground Growth Responses of Loblolly Pine to Nutrient and Water Additions , 1998, Forest Science.

[35]  P. Roberntz,et al.  Effects of elevated CO(2) concentration and nutrition on net photosynthesis, stomatal conductance and needle respiration of field-grown Norway spruce trees. , 1998, Tree physiology.

[36]  S. Kellomäki,et al.  Effects of long-term CO2 and temperature elevation on crown nitrogen distribution and daily photosynthetic performance of Scots pine , 1997 .

[37]  D. Whitehead,et al.  The response of photosynthetic model parameters to temperature and nitrogen concentration in Pinus radiata D. Don , 1997 .

[38]  T. C. Hennessey,et al.  Acclimation of loblolly pine (Pinus taeda) foliage to light intensity as related to leaf nitrogen availability , 1997 .

[39]  M. Strand Effect of mineral nutrition content on oxygen exchange and chlorophyll a fluorescence in needles of Norway spruce. , 1997, Tree physiology.

[40]  H. L. Allen,et al.  Effects of carbon dioxide, fertilization, and irrigation on photosynthetic capacity of loblolly pine trees. , 1996, Tree physiology.

[41]  M. G. Ryan,et al.  Foliage, fine-root, woody-tissue and stand respiration in Pinus radiata in relation to nitrogen status. , 1996, Tree physiology.

[42]  D. Tissue,et al.  Long‐term effects of elevated CO2 and nutrients on photosynthesis and rubisco in loblolly pine seedlings , 1993 .

[43]  T. Hinckley,et al.  Effects of foliar nitrogen concentration on photosynthesis and water use efficiency in Douglas-fir. , 1993, Tree physiology.

[44]  J. Seiler,et al.  Physiological and Growth Responses of Eight-Year-Old Loblolly Pine Stands to Thinning , 1991 .

[45]  H. L. Allen,et al.  Seedling shoot growth of loblolly pine families under two nitrogen levels as related to 12-year height , 1991 .

[46]  H. L. Allen,et al.  Genetic variation in nitrogen use efficiency of loblolly pine seedlings , 1991 .

[47]  H. L. Allen,et al.  Leaf Area, Stemwood Growth, and Nutrition Relationships in Loblolly Pine , 1988, Forest Science.

[48]  E. Axelsson,et al.  Changes in carbon allocation patterns in spruce and pine trees following irrigation and fertilization. , 1986, Tree physiology.

[49]  S. Palmroth,et al.  Short-term effects of fertilization on photosynthesis and leaf morphology of field-grown loblolly pine following long-term exposure to elevated CO(2) concentration. , 2008, Tree physiology.

[50]  M. I C H A E,et al.  Carbon allocation in forest ecosystems , 2007 .

[51]  A. T,et al.  Strategies and Case Studies for Incorporating Ecophysiology into Southern Pine Tree Improvement Programs , 2005 .

[52]  L. Samuelson Effects of nitrogen on leaf physiology and growth of different families of loblolly and slash pine , 2004, New Forests.

[53]  C. Gough,et al.  Seasonal Photosynthesis in Fertilized and Nonfertilized Loblolly Pine , 2004 .

[54]  G. Bauera,et al.  Effects of chronic N additions on tissue chemistry , photosynthetic capacity , and carbon sequestration potential of a red pine ( Pinus resinosa Ait . ) stand in the NE United States , 2004 .

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

[56]  M. Adams,et al.  Phosphorus affects growth and partitioning of nitrogen to Rubisco in Pinus pinaster. , 2002, Tree physiology.

[57]  Kurt H. Johnsen,et al.  Ideotype Development in Southern Pines: Rationale and Strategies for Overcoming Scale-Related Obstacles , 2001 .

[58]  W. Smith,et al.  Interrelationships among light, photosynthesis and nitrogen in the crown of mature Pinus contorta ssp. latifolia. , 1999, Tree physiology.

[59]  H. L. Allen,et al.  Effects of site preparation, early fertilization, and weed control on 14-year old loblolly pine , 1998 .

[60]  H. L. Allen,et al.  Nitrogen and Family Effects on Biomass Allocation of Loblolly Pine Seedlings , 1991, Forest Science.

[61]  R. K. Dixon,et al.  An optimal sampling strategy for determining CO2 exchange rate as a function of photosynthetic photon flux density , 1987 .

[62]  Bobby M. Long,et al.  Soil survey of Berkeley County, South Carolina , 1980 .