Relative growth and nutrient accumulation rates for tobacco |
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Authors: | C David Raper Jr David T Patterson Lawrence R Parsons Paul J Kramer |
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Institution: | (1) Department of Soil Science, North Carolina State University, Raleigh, North Carolina, U.S.A.;(2) Department of Botany, Duke University, Durham, North Carolina, U.S.A.;(3) Present address: Department of Horticulture, University of Minnesota, St. Paul, Minnesota, U.S.A. |
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Abstract: | Summary Tobacco plants (Nicotiana tabacum L.) were grown from transplanting until floral expression in the phytotron units of Southeastern Plant Environment Laboratories
to evaluate the relationship between relative growth rate (RGR) and relative accumulation rates (RAR) of N, P, K, Ca, and
Mg. RAR is calculated to be analogous to RGR. Plants were grown in both controlled-environment rooms with artificial light
and air-conditioned greenhouses with natural light at three temperature conditions and three application rates of N-P-K. RGR
and RAR were calculated only for the period of grand growth which occurred within the interval from 7 to 32 days after transplanting.
In general, neither RGR nor RAR were affected by temperature or nutrient level. However, both temperature and nutrient level
affected dry matter accumulation of the plants apparently by an influence on the rapidity with which plants adjusted to their
new environment during the initial 7-day interval after transplanting. RAR for P and K were coequal with RGR of the whole
plant; thus, the concentrations of P and K within the plant tended to remain constant during growth. RAR for N, Ca, and Mg
were less than RGR for the whole plant; thus, internal concentrations of these nutrients declined during growth. RAR of N,
Ca, and Mg for the whole plant were equivalent to RGR of the roots. As a rationale for the association of RGR of roots and
RAR of N, it is proposed that the soluble carbohydrate pool in the roots concurrently influences both N absorption, as NO3
-, and growth of new roots of immature plants.
Research reported in this paper was supported in part by National Science Foundation (RANN) Grants GI-39229 and GI-39230.
Operation of the Phytotron Units of Southeastern Plant Environmental Laboratories at Duke and North Carolina State Universities
was supported by National Science Foundation Grants GB-28950-1A and GI-28951. Approved as Paper Number 4773 of the Journal Series of the North Carolina Agricultural Experiment Station, Raleigh, NC.
Research reported in this paper was supported in part by National Science Foundation (RANN) Grants GI-39229 and GI-39230.
Operation of the Phytotron Units of Southeastern Plant Environmental Laboratories at Duke and North Carolina State Universities
was supported by National Science Foundation Grants GB-28950-1A and GI-28951. Approved as Paper Number 4773 of the Journal Series of the North Carolina Agricultural Experiment Station, Raleigh, NC. |
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