THE EFFECT OF AGE ON NET ASSIMILATION AND RELATIVE GROWTH RATES IN THE COTTON PLANT

1937 ◽  
Vol 1 (3) ◽  
pp. 565-566 ◽  
Author(s):  
O. V. S. HEATH
1967 ◽  
Vol 69 (3) ◽  
pp. 305-315 ◽  
Author(s):  
J. E. Jackson

Growth analysis of cotton crops sown in the Sudan Gezira at monthly intervals between August and May revealed a marked seasonal pattern of growth. Irrespective of plant age and fruiting state growth of non-senescent plants was slowest during the cool winter months. Relative growth rates of young plants were highest in August, September and early October due to the high specific leaf areas and fairly high net assimilation rates found then. They were lowest when minimum temperatures were lowest. Net assimilation rates were also lowest in the coolest months, probably as a result of restricted growth. High temperatures in the spring reduced fruiting. It is concluded that low minimum temperatures and high evaporation rates are both associated with slow growth, and play a large part in determining the characteristic decline of growth rates of cotton sown at the usual date in August.I wish to thank the Chief of the Research Division, Ministry of Agriculture, Sudan, for permission to publish this paper and to record my gratitude to the team of field and laboratory assistants, especially Salih Saad and Hassan Osman, who helped in the work.


1969 ◽  
Vol 49 (4) ◽  
pp. 465-470
Author(s):  
D. B. Wilson ◽  
A. Johnston

Seedlings of a native grass, rough fescue, Festuca scabrella Torr., and of a tame grass, tall fescue, Festuca arundinacea Schreb., were grown in the greenhouse for 10 weeks. Each week 20 plants of each species were destructively harvested for growth analysis. Leaf and tiller numbers and leaf lengths were recorded for an additional 10 plants of each species. Mean net assimilation rates of rough fescue were similar to those of tall fescue, but leaf area ratios were significantly lower. Thus, mean relative growth rates of rough fescue were less than those of tall fescue. Tiller numbers were similar for both species but rough fescue produced fewer leaves. Dry weight of tops of the tame grass produced during the 10-week period was about 17 times that produced by the native grass.


1975 ◽  
Vol 26 (3) ◽  
pp. 447 ◽  
Author(s):  
EK Christie

The optimum temperature for vegetative growth of mulga grass was about 25°C, and for Mitchell and buffel grasses 30°. Buffel grass had the highest yield at all temperatures, partly because of its higher growth rate which in turn can be ascribed to both a higher net assimilation rate and the diversion of a greater proportion of dry weight into leaf area. Seedlings with an ample supply of phosphate had higher relative growth rates than phosphorus-deficient seedlings at the commencement of the soil drying cycle, but their growth rates declined more rapidly as the soil water potential fell. This decline was associated with a reduction in the rate of phosphate absorption as well as a decrease in the tissue phosphorus concentration. *Part II, Aust. J. Agric. Res., 26: 437 (1975).


1996 ◽  
Vol 26 (9) ◽  
pp. 1556-1568 ◽  
Author(s):  
Thimmappa S. Anekonda ◽  
Richard S. Criddle ◽  
Lee D. Hansen ◽  
Mike Bacca

Seventeen Eucalyptus species and 30 rapid-growing Eucalyptuscamaldulensis trees (referred to as plus trees), growing in a plantation were studied to examine relationships among measured plant growth and respiratory parameters, geographical origins, and growth climate. The respiratory parameters measured at two different temperatures by isothermal calorimetry were metabolic heat rate, rate of CO2 production, and the ratio of heat rate to CO2 rate. Metabolic heat rate was also measured as a continuous function of temperature by differential scanning calorimetry in the range of 10 to 40 °C. Tree growth was measured as rates of height and stem volume growth. The values of respiratory and growth variables of Eucalyptus species are significantly correlated with latitude and altitude of origin of their seed sources. The maximum metabolic heat rate, the temperature of the maximum heat rate, the temperature coefficients of metabolic rate, and the temperatures at which the slopes of Arrhenius plots change are all genetically determined parameters that vary both within and among species. Measurement of growth rate–respiration rate–temperature relationships guide understanding of why relative growth rates of Eucalyptus species and individual genotypes differ with climate, making it possible to identify genotypes best suited for rapid growth in different climates. The temperature dependence of respiration rates is an important factor determining relative growth rates of eucalypts in different climates. To achieve optimum biomass production the temperature dependence of individual plants must be matched to growth climate.


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