Latitude and Relative Growth in the Razor Clam, Siliqua Patula

1931 ◽  
Vol 8 (3) ◽  
pp. 228-249
Author(s):  
F. W. WEYMOUTH ◽  
H. C. McMILLIN ◽  
WILLIS H. RICH
Keyword(s):  
Growth Rate ◽  
Life Span ◽  
Relative Growth Rate ◽  
Growth Data ◽  
Natural Conditions ◽  
Relative Growth ◽  
Absolute Growth Rate ◽  
Mathematical Expressions ◽  
Wide Range ◽  
Absolute Growth

1. The present paper is a study of the growth of a clam (Siliqua patula) under natural conditions and over a wide range of latitude. 2. Various constants derived from the growth data are compared for the different localities. For this species, over the range considered, growth in the southern localities as compared with the northern is initially more rapid but less sustained, leads to a smaller total length and is associated with a shorter life span. 3. Reasons are presented for considering the relative growth-rate as a particularly significant constant leading to more sound biological conclusions than the use of the absolute growth-rate. 4. On the basis of the relative growth-rate, current mathematical expressions for the course of growth are discussed and a formula used which emphasises Minot's conception of a growth-rate constantly declining with age. This expression L = Be-ce-ce-kt, in which L = length at time t, e = base of natural logarithms, and B, c and k are constants, is found to graduate the extensive data in clam growth with significant accuracy.

scholarly journals Growth of the crabgrass species Digitaria ciliaris and Digitaria nuda

2012 ◽  
Vol 30 (2) ◽  
pp. 317-325 ◽  
Author(s):  
R.C. Souza ◽  
A.C. Dias ◽  
M.R.A. Figueiredo ◽  
F.E.B. Obara ◽  
P.J Christoffoleti
Keyword(s):  
Growth Rate ◽  
Leaf Area ◽  
Relative Growth Rate ◽  
Dry Matter ◽  
Area Ratio ◽  
Leaf Area Ratio ◽  
Leaf Number ◽  
Relative Growth ◽  
Absolute Growth Rate ◽  
Absolute Growth

The aim of this research paper was to compare the growth of D. ciliaris and D. nuda crabgrass species under non-competitive conditions. To this end, two experiments were conducted, one from March - July 2010 and the other from February - June 2011. The experimental design of both trials was completely randomized making a factorial (2 seasons x 2 species crabgrass x 12 evaluation periods) with four replications. Assessments began at 15 days after sowing (DAS), and repeated weekly until 92 DAS. The variables evaluated were total dry matter (roots+leaves+stems), leaf area, leaf number and tiller. The results were submitted to analysis of variance and the absolute growth rate, relative growth rate and leaf area ratio were calculated using the means, which were adjusted regression models. The crabgrass species were significantly different in leaf area, leaf number, tiller number and dry matter per plant. D. ciliaris for all variables was statistically higher than D. nuda. Regarding the speed at which the growth of the species occurred, the absolute growth rate and relative growth rate of D. ciliaris was also greater than D. nuda. In addition, D. ciliaris also had a lower leaf area ratio indicating greater efficiency in converting light energy into carbohydrates. It can be concluded that D. ciliaris has a higher growth rate in conditions where there is no limitation of nutrients and water availability in relation to D. nuda, mainly due to D. ciliaris have greater leaf area, number of leaves and dry matter accumulation per plant.

Functional growth analysis of red pine trees under variable intensities of competition

1998 ◽  
Vol 74 (5) ◽  
pp. 728-735 ◽  
Author(s):  
Guy R. Larocque
Keyword(s):  
Growth Rate ◽  
Relative Growth Rate ◽  
Pinus Resinosa ◽  
Functional Approach ◽  
Red Pine ◽  
Tree Size ◽  
Relative Growth ◽  
Crown Width ◽  
Absolute Growth Rate ◽  
Absolute Growth

A functional approach is proposed for comparing the development of individual red pine (Pinus resinosa Ait.) trees which had been growing under different intensities of competition from ages 13 to 43. Growth rate measures, based on absolute growth rate, relative growth rate and the ratio of absolute growth rate to crown width, were obtained from the differentiation of a cumulative growth function. Individual tree data were obtained from stands of the same age, but with different initial spacings: 1.5 × 1.5 m, 2.4 × 2.4 m, and 4.3 × 4.3 m. The Chapman-Richards function represented adequately the growth trends of individual trees. While cumulative growth indicated a fairly consistent pattern, that is, the bigger the tree initially, the bigger it remained, absolute growth rate was not related to tree size. Some of the smallest trees had the greatest absolute growth rate. Relative growth rate was more informative on the effect of competition. Before competition became severe, small trees had greater relative growth rates than large trees, and the effect of competition was to reverse this trend. The ratio of absolute growth rate to crown width indicated that the ability of trees to occupy the aerial growing space was not related to tree size. Key words: red pine (Pinus resinosa Ait.), growth functions, absolute growth rate, relative growth rate, functional approach

THE RATE OF DRY WEIGHT ACCUMULATION IN MARQUIS WHEAT AS AFFECTED BY TEMPERATURE AND LIGHT INTENSITY

1962 ◽  
Vol 40 (7) ◽  
pp. 939-955 ◽  
Author(s):  
D. J. C. Friend ◽  
V. A. Helson ◽  
J. E. Fisher
Keyword(s):  
Growth Rate ◽  
Light Intensity ◽  
Relative Growth Rate ◽  
Growth Period ◽  
Dry Weight ◽  
Continuous Illumination ◽  
Relative Growth ◽  
Absolute Growth Rate ◽  
Absolute Growth ◽  
The Mean

Plants were grown to the stage of anthesis at constant temperatures from 10 to 30 °C and under continuous illumination at intensities ranging from 200 to 2500 ft-c. The absolute growth rate was maximal at the time of ear emergence. The relative growth rate declined continuously with time; the rate of decline was greatest at the higher temperatures and light intensities. The optimal temperature for the mean absolute growth rate over the whole growth period was 20–25 °C. The optimum for the mean relative growth rate was 15–20 °C. This difference is attributed to the faster rate of floral development at high temperatures. Both absolute and relative growth rates increased with increasing light intensity up to 2500 ft-c.

Analyzing growth in cell cultures. I. Calculating growth rates

1986 ◽  
Vol 64 (1) ◽  
pp. 233-237 ◽  
Author(s):  
Susan R. Singer
Keyword(s):  
Growth Rate ◽  
Relative Growth Rate ◽  
Growth Rates ◽  
Rate Equations ◽  
Constant Growth Rate ◽  
Relative Growth ◽  
Relative Growth Rates ◽  
Growing Cell ◽  
Absolute Growth ◽  
Plant Tissue Cultures

Growth is the major parameter used to assess novel phenotypes derived from plant tissue cultures. Any quantitative analysis of growth must have an explicit rational basis. Frequently this criterion is not met. For example, the calculation (W2 − W1)/W1(W1 = initial weight; W2 = final weight) approximates neither linear nor exponential growth. Yet, it is a common method of analysis, as is the related calculation W2/W1. When absolute growth values provide insufficient information, meaningful relative growth rate equations can be utilized. Relative growth rates should be evaluated as ln (W2/W1)/(t2 − t1) for t = time, thereby yielding a constant growth rate for exponentially growing cell lines. Linear growth (root growth, for example) can be approximated by 2(W2 − W1)/((W1 + W2)(t2 − t1)). All methods of analysis we have encountered assume that relative growth at a given instant depends on total mass. The possibility exists that growth may actually be proportional to mass raised to some power less than one. For example, growth could be limited to a thin outer shell of a spherical callus. Then the relative growth rate would equal 3(W21/3 − W11/3)/(t2 − t1). Data can be seriously distorted when inappropriate calculations are used. Such distortions are exacerbated when comparisons are made. In all cases an adequate assessment of growth kinetics for each cell line and each treatment is essential.

Stem anatomy and relative growth rate in seedlings of a wide range of woody plant species and types

Oecologia ◽  
1998 ◽  
Vol 116 (1-2) ◽  
pp. 57-66 ◽  
Author(s):  
P. Castro-Díez ◽  
J. P. Puyravaud ◽  
J. H. C. Cornelissen ◽  
P. Villar-Salvador
Keyword(s):  
Growth Rate ◽  
Relative Growth Rate ◽  
Plant Species ◽  
Woody Plant ◽  
Stem Anatomy ◽  
Relative Growth ◽  
Woody Plant Species ◽  
Wide Range

GROWTH RATES, HARVEST INDEX AND MOISTURE USE OF MANITOU SPRING WHEAT AS INFLUENCED BY NITROGEN, TEMPERATURE AND MOISTURE

1984 ◽  
Vol 64 (4) ◽  
pp. 825-839 ◽  
Author(s):  
H. R. DAVIDSON ◽  
C. A. CAMPBELL
Keyword(s):  
Growth Rate ◽  
Spring Wheat ◽  
Growth Rates ◽  
Harvest Index ◽  
Net Photosynthesis ◽  
Moisture Stress ◽  
Growth Stages ◽  
Relative Growth ◽  
Absolute Growth Rate ◽  
Absolute Growth

Manitou spring wheat (Triticum aestivum L.) was grown at combinations of three day/night temperatures (27/12 °C (T27), 22/12 °C (T22) and 17/12 °C (T17)), three levels of fertilizer N (58, 116 and 174 kg/ha), and three moisture stresses (nominally −0.03, −1.5 and −4.0 MPa) applied for four durations (viz., no stress throughout, stress from (i) four-tiller (Tg), (ii) near ligule of last leaf visible (LLV), or (iii) flowering (F1) stages to harvest (Hvst)). Weights of plant parts and photosynthetic area of leaves and stems were measured at eight growth stages. Mean net rate of photosynthesis [Formula: see text] was estimated by dividing plant dry weight by photosynthetic area duration. Temperature was the main factor affecting net photosynthesis and growth. Under optimum moisture and fertility, net photosynthesis was inversely related to temperature being 1.15, 1.19 and 1.29 μg∙cm−2∙day−1 at T27, T22 and T17, respectively. However, absolute growth rates were highest at T22. For example, at low moisture stress and N174, absolute growth rates were 0.69, 0.77 and 0.66 g∙day−1 at T27, T22 and T17, respectively. High moisture stress from Tg to maturity reduced absolute growth rate by about 60%. Low N rates also reduced absolute growth rate. Relative growth rate was constant and highest between emergence and LLV; it then declined rapidly and was negative after soft dough. It was suggested that the absolute growth rates and relative growth rates generated in this study could be adapted for use in simulation modelling exercises. Moisture stress was the most important factor influencing the proportion of the plant’s weight that was harvested in the grain (harvest index). Moisture stress from Tg to harvest resulted in a harvest index of 0.34 ± 0.03; for all other treatments the index was 0.28 ± 0.01. The rate and amount of water used by the plants was greatest at T27 and lowest at T22, consequently water use effeciency was lowest at T27 and highest at T22.Key words: Net photosynthesis, growth kinetics of wheat, leaf area duration

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