Effect of Temperature on Growth of Five Subtropical Grasses. I. Effect of Day and Night Temperature on Growth and Morphological Development

1978 ◽  
Vol 5 (2) ◽  
pp. 131 ◽  
Author(s):  
DA Ivory ◽  
PC Whiteman
Keyword(s):  
Growth Rate ◽  
Diurnal Variation ◽  
Constant Temperature ◽  
Growth Rates ◽  
Leaf Growth ◽  
Maximum Growth ◽  
Effect Of Temperature ◽  
Panicum Maximum ◽  
Morphological Development ◽  
Night Temperature

Cenchrus ciliaris, Chloris gayana, Panicum maximum var, trichoglume, Panicum coloratum var. makarikariense and Pennisetum clandestinum were grown in two experiments in controlled environments, each experiment having all possible day/night temperature combinations of (1) 10, 20, 30, and 40°C and (2) 15,25, 30 and 35°C. Both day and night temperatures significantly affected growth in all species. Growth was greatly restricted by constant temperatures of 10 and 15°, while maximum growth rates occurred at 29-35°C day temperatures with 26-30°C night temperatures. At optimum or supra-optimum temperatures a diurnal variation in temperature gave higher growth rates than a constant temperature for the same daily mean. By contrast, at suboptimum temperatures a constant temperature gave the highest growth rates and growth rate was decreased as the diurnal variation about a given daily mean temperature was increased. Mathematical functions relating the growth of each species to day and night temperature and maximum growth rate at optimum temperatures were developed. The effect of temperature on relative growth rate (Rw) was mediated through its effect on net assimilation rate (EA). Night temperature was found to affect Rw and EA independently of day temperature and therefore a prehistory effect of night temperature on photosynthesis in the subsequent day was indicated. Temperature had significant effects on tillering in P. maximum and P. clandestinum but had little effect in C. gayana, C. ciliaris and P. coloratum. The optimum temperatures for leaf growth and leaf area development in C. ciliaris and C. gayana were higher than the optimum temperatures for growth of the whole plant, while optimum temperatures for stem growth were lower. In P. maximum, P. coloratum and P. clandestinum, optimum temperatures for all growth components were similar. Differences between temperate and tropical grasses in morphological reaction to temperature are discussed.

Shoot and leaf growth in Fraxinuspennsylvanica and its relation to crown location and pruning

1994 ◽  
Vol 24 (10) ◽  
pp. 1997-2005 ◽  
Author(s):  
W.R. Remphrey ◽  
C.G. Davidson
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Leaf Growth ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Logistic Growth ◽  
Parameter Estimates ◽  
Regression Equations ◽  
Green Ash ◽  
Growth Duration

Elongation of shoots in various crown locations, and of individual internodes and leaves of the leading shoot, were recorded at 2-day intervals throughout the 1991 growing season in four clones of Fraxinuspennsylvanica var. subintegerrima (Vahl) Fern. (green ash). Other trees were disbudded and pruned to a single leader. Using a logistic growth function, nonlinear regression equations were generated and parameter estimates were used to determine maximum growth rates. Terminal leading shoots had a longer growth duration and a greater maximum growth rate than lateral shoots. The pruning treatment resulted in larger shoots, which grew 2–3 weeks longer and had a higher maximum growth rate. Leaf emergence occurred at regular intervals but the rate of emergence varied among clones. Leaf maximum growth rates were not significantly different among clones. Leaf size declined acropetally whereas internode length increased and then decreased. The longest leaves and internodes had the highest maximum growth rates. The size and maximum growth rates of putative preformed leaves were larger than putative neoformed leaves. As a shoot expanded, growth of one internode tended to cease during the linear phase of growth of its associated leaf and that of the succeeding internode.

Comparison of copper sulphate pentahydrate growth rates determined by different methods

1990 ◽  
Vol 55 (7) ◽  
pp. 1691-1707 ◽  
Author(s):  
Miloslav Karel ◽  
Jiří Hostomský ◽  
Jaroslav Nývlt ◽  
Axel König
Keyword(s):  
Growth Rate ◽  
Crystal Growth ◽  
Fluidized Bed ◽  
Growth Rates ◽  
Copper Sulphate ◽  
Crystal Growth Rate ◽  
Effect Of Temperature ◽  
Rotating Disc ◽  
Shape Factors ◽  
Data Treatment

Crystal growth rates of copper sulphate pentahydrate (CuSO4.5 H2O) determined by different authors and methods are compared. The methods included in this comparison are: (i) Measurement on a fixed crystal suspended in a streaming solution, (ii) measurement on a rotating disc, (iii) measurement in a fluidized bed, (iv) measurement in an agitated suspension. The comparison involves critical estimation of the supersaturation used in measurements, of shape factors used for data treatment and a correction for the effect of temperature. Conclusions are drawn for the choice of values to be specified when data of crystal growth rate measurements are published.

Reassessment of Maximum Growth Rates for C3 and C4 Crops

1978 ◽  
Vol 14 (1) ◽  
pp. 1-5 ◽  
Author(s):  
J. L. Monteith
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Growing Season ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Crop Growth ◽  
Close Inspection ◽  
Similar Difference ◽  
Photosynthetic Efficiencies

SUMMARYFigures for maximum crop growth rates, reviewed by Gifford (1974), suggest that the productivity of C3 and C4 species is almost indistinguishable. However, close inspection of these figures at source and correspondence with several authors revealed a number of errors. When all unreliable figures were discarded, the maximum growth rate for C3 stands fell in the range 34–39 g m−2 d−1 compared with 50–54 g m−2 d−1 for C4 stands. Maximum growth rates averaged over the whole growing season showed a similar difference: 13 g m−2 d−1 for C3 and 22 g m−2 d−1 for C4. These figures correspond to photosynthetic efficiencies of approximately 1·4 and 2·0%.

Single Crystal Silicon Carbide On Silicon Using A Supersonic Gas Jet Of Methylsilane

1997 ◽  
Vol 483 ◽  
Author(s):  
S. A. Ustin ◽  
C. Long ◽  
L. Lauhon ◽  
W. Ho
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Single Crystal Silicon ◽  
Maximum Growth ◽  
X Ray Diffraction ◽  
Crystal Silicon ◽  
Cross Sectional ◽  
Supersonic Molecular Beam ◽  
Transmission Electron

AbstractCubic SiC films have been grown on Si(001) and Si(111) substrates at temperatures between 600 °C and 900 °C with a single supersonic molecular beam source. Methylsilane (H3SiCH3) was used as the sole precursor with hydrogen and nitrogen as seeding gases. Optical reflectance was used to monitor in situ growth rate and macroscopic roughness. The growth rate of SiC was found to depend strongly on substrate orientation, methylsilane kinetic energy, and growth temperature. Growth rates were 1.5 to 2 times greater on Si(111) than on Si(001). The maximum growth rates achieved were 0.63 μm/hr on Si(111) and 0.375μm/hr on Si(001). Transmission electron diffraction (TED) and x-ray diffraction (XRD) were used for structural characterization. In-plane azimuthal (ø-) scans show that films on Si(001) have the correct 4-fold symmetry and that films on Si(111) have a 6-fold symmetry. The 6-fold symmetry indicates that stacking has occurred in two different sequences and double positioning boundaries have been formed. The minimum rocking curve width for SiC on Si(001) and Si(111) is 1.2°. Fourier Transform Infrared (FTIR) absorption was performed to discern the chemical bonding. Cross Sectional Transmission Electron Microscopy (XTEM) was used to image the SiC/Si interface.

Dynamic Predictive Model for Growth of Bacillus cereus from Spores in Cooked Beans

2017 ◽  
Vol 81 (2) ◽  
pp. 308-315 ◽  
Author(s):  
Vijay K. Juneja ◽  
Abhinav Mishra ◽  
Abani K. Pradhan
Keyword(s):  
Bacillus Cereus ◽  
Growth Rates ◽  
Linear Models ◽  
Growth Models ◽  
Maximum Growth ◽  
Effect Of Temperature ◽  
Coefficient Of Determination ◽  
Growth Data ◽  
Three Phase ◽  
Primary Model

ABSTRACT Kinetic growth data for Bacillus cereus grown from spores were collected in cooked beans under several isothermal conditions (10 to 49°C). Samples were inoculated with approximately 2 log CFU/g heat-shocked (80°C for 10 min) spores and stored at isothermal temperatures. B. cereus populations were determined at appropriate intervals by plating on mannitol–egg yolk–polymyxin agar and incubating at 30°C for 24 h. Data were fitted into Baranyi, Huang, modified Gompertz, and three-phase linear primary growth models. All four models were fitted to the experimental growth data collected at 13 to 46°C. Performances of these models were evaluated based on accuracy and bias factors, the coefficient of determination (R2), and the root mean square error. Based on these criteria, the Baranyi model best described the growth data, followed by the Huang, modified Gompertz, and three-phase linear models. The maximum growth rates of each primary model were fitted as a function of temperature using the modified Ratkowsky model. The high R2 values (0.95 to 0.98) indicate that the modified Ratkowsky model can be used to describe the effect of temperature on the growth rates for all four primary models. The acceptable prediction zone (APZ) approach also was used for validation of the model with observed data collected during single and two-step dynamic cooling temperature protocols. When the predictions using the Baranyi model were compared with the observed data using the APZ analysis, all 24 observations for the exponential single rate cooling were within the APZ, which was set between −0.5 and 1 log CFU/g; 26 of 28 predictions for the two-step cooling profiles also were within the APZ limits. The developed dynamic model can be used to predict potential B. cereus growth from spores in beans under various temperature conditions or during extended chilling of cooked beans.

The Effect of Temperature on the Growth and Respiration of Fish Embryos (Salmo Fario)

1932 ◽  
Vol 9 (3) ◽  
pp. 271-276
Author(s):  
A. H. WOOD
Keyword(s):  
Growth Rate ◽  
Oxygen Consumption ◽  
Relative Intensity ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Effect Of Temperature ◽  
Total Oxygen ◽  
Average Efficiency ◽  
Complete Development ◽  
Time Required

1. The rate of respiration (as expressed in c.c. O2 per gram embryo per hour) of the embryos of Salmo fario remains constant at any given temperature until the embryo has reached its maximum growth-rate, after this point it declines. It is suggested that the rate of respiration may be proportional to the amount of available yolk. 2. When incubated at 7° C. the time required to complete development after hatching was 58 days and the total oxygen consumed by an average embryo during this period was 20·31 c.c. (N.T.P.). At 12° the time required for the completion of development was reduced to 27 days, but the oxygen consumption remained practically unchanged at 20·71 c.c. At 3° C. the time required for development was 108 days and the oxygen consumption was 26·96 c.c. per embryo. 3. At 7 and 12° C. the efficiency of development was found to be identical with the value given by Gray for 11·5° C., viz. 63 per cent.; at 3°C. the average efficiency over the period considered was only 54 per cent. 4. It is suggested that, between the limits of temperature to which a trout egg is normally exposed, the effect of temperature on respiration is neither greater nor less than its effect on the growth-rate; possibly both processes are dependent on the same controlling factor. Above and below this range of temperature, the relative intensity of the respiratory processes (to those of growth) is increased, and a smaller embryo is the final result of incubation.

Kinetics And Morphology Of Homoepitaxial Cvd Growth On Diamond (100) And (111)

1995 ◽  
Vol 416 ◽  
Author(s):  
R. E. Rawles ◽  
W. G. Morris ◽  
M. P. D’Evelyn
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Chemical Vapor ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Arrhenius Behavior ◽  
Oriented Growth ◽  
Relative Growth Rates ◽  
Cvd Growth ◽  
Hot Filament

ABSTRACTGrowth rates for homoepitaxy of diamond (100) and (111) by hot-filament chemical vapor deposition were measured via in situ Fizeau interferometry and the surface morphologies were subsequently characterized by atomic force microscopy (AFM). (100)-oriented growth from 0.5% CH4 in H2 exhibited pure Arrhenius behavior, with an activation energy of 17±1 kcal/mol, up to a substrate temperature of 1100°C. Addition of oxygen to the feed gas resulted in an increased growth rate below 900°C, a maximum growth rate between 900 and 1000°C, and etching (of diamond) above 1050 - 1100°C. However, the presence of oxygen apparently had less effect on the surface morphology than did the (100)-to-(111) growth rate parameter α, determined directly from the relative growth rates of (100) and (111) substrates mounted side by side. During homoepitaxial growth from 0.5% CH4 in H2 at 875°C of ca. 1-micron-thick films,α = was 2.2 without oxygen and 1.3 for growth with 0.14% O2. The (100) film grown with α = 2.2 was quite smooth, while that with α = 1.3 was covered by numerous hillocks and penetration twins. AFM analysis revealed surprisingly little difference between the (111) films despite the considerable difference in α. Implications of these results for the growth mechanism are discussed.

Growth Rate Responses of Lotic Periphytic Diatoms to Experimental Phosphorus Enrichment: The Influence of Temperature and Light

1988 ◽  
Vol 45 (2) ◽  
pp. 261-270 ◽  
Author(s):  
Max L. Bothwell
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Phosphorus Enrichment ◽  
Enrichment Experiments ◽  
Community Growth ◽  
Specific Growth Rates ◽  
The Relationship ◽  
River Water Temperature

Phosphate enrichment experiments were conducted year-round at the experimental troughs research apparatus (EXTRA) on the South Thompson River in British Columbia to determine the relationship between external concentration of orthophosphate and the growth rates of lotic periphytic diatom communities. Growth rate saturation always occurred at a phosphate concentration of approximately 0.3–0.6 μg P∙L−1. The maximum growth rate (μmax-P) with phosphorus enrichment varied seasonally with temperature. The relative specific growth rates (μ:μmax-P) as a function of external phosphate were constant. Seasonal changes in solar insolation (PAR) had no effect on the autotrophic community growth rates in unamended river water. Temperature exerted the most dominant influence on phosphorus-replete growth rates.

The effect of temperature on the relative leaf growth rate of crops of vicia faba L

1978 ◽  
Vol 19 (6) ◽  
pp. 505-514 ◽  
Author(s):  
M.D. Dennett ◽  
J.R. Milford ◽  
J. Elston
Keyword(s):  
Growth Rate ◽  
Vicia Faba ◽  
Leaf Growth ◽  
Effect Of Temperature ◽  
Vicia Faba L

Studies of grain production in Sorghum bicolor (L. Moench). V.* Effect of planting density on growth and yield

1975 ◽  
Vol 26 (1) ◽  
pp. 31 ◽  
Author(s):  
KS Fischer ◽  
GL Wilson
Keyword(s):  
Growth Rate ◽  
Grain Yield ◽  
Leaf Area ◽  
Growth Rates ◽  
Dry Matter ◽  
Leaf Growth ◽  
Crop Growth ◽  
Area Index ◽  
Crop Growth Rate ◽  
Net Assimilation

Growth analysis was applied to grain sorghum (cv. RS610) grown at low, medium and high population densities, i.e. 14,352, 143,520 and 645,836 plants ha-1 respectively. The medium densities had two arrangements of plants, square (S) and rectangular (R). Crop growth rates, inflorescence growth rates, leaf area indices, net assimilation rates and leaf growth rates were calculated from growth functions of plant dry matter and leaf area over time. Differences in crop growth rate between populations in the early stages were attributed to leaf area development—specifically to the initial leaf area (dependent on seedling number) and not to differences in leaf growth rates. Peak crop growth rates were 15.0, 27.5, 26.0 and 45.8 g m-2 day-1 for the low, medium (S), medium (R) and high populations respectively.The large difference between the growth rates of the medium (S) and the high populations was not explained by differences in the amount of radiation intercepted. Although leaf area indices were 4.6 and 10.2 respectively for the two populations, both canopies intercepted almost all of the noon radiation. Light extinction coefficients were 0.45 and 0.29 respectively. The relationship between net assimilation rate and leaf area index was such that for comparable leaf area indices above 2, plants at higher densities showed greater improvement in yield per unit increment in leaf area index. A maximum grain yield of 14,250 kg ha-1 was obtained at the high population density as a result of higher dry matter production, but a similar harvest index to that of the crops grown at the other densities. Inflorescence growth rate (g m-2 day-l) slightly exceeded crop growth rate in the latter part of grain filling, which indicated that there was some retranslocation to the grain of previously assimilated material. The maximum grain yield represents an efficiency of utilization of short-wave solar radiation during crop life of 2.5 x 10-6g cal-1. *Part IV, Aust. J. Agric. Res., 26: 25 (1975).

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