Absolute growth rates

1990 ◽  
pp. 17-24 ◽  
Author(s):  
Roderick Hunt
Keyword(s):  
Growth Rates ◽  
Absolute Growth

scholarly journals Age, growth, and recruitment patterns of juvenile ladyfish (Elopssp) from the east coast of Florida (USA)

PeerJ ◽  
2015 ◽  
Vol 3 ◽  
pp. e1392
Author(s):  
Juan C. Levesque
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Age And Growth ◽  
Growth Equation ◽  
Length Frequency ◽  
Daily Growth ◽  
Exponential Regression ◽  
Absolute Growth ◽  
Specific Growth Rates ◽  
Size At Age

Ladyfish (Elopssp) are a common and economically valuable coastal nearshore species found along coastal beaches, bays, and estuaries of the southeastern United States, and subtropical and tropical regions worldwide. Previously, ladyfish were a substantial bycatch in Florida’s commercial fisheries, but changes in regulations significantly reduced commercial landings. Today, ladyfish are still taken in commercial fisheries in Florida, but many are also taken by recreational anglers. Life-history information and research interest in ladyfish is almost non-existent, especially information on age and growth. Thus, the overarching purpose of this study was to expand our understanding of ladyfish age and growth characteristics. The specific objectives were to describe, for the first time, age, growth, and recruitment patterns of juvenile ladyfish from the east coast of Florida (USA). In the Indian River Lagoon (IRL), annual monthly length-frequency distributions were confounded because a few small individuals recruited throughout the year; monthly length-frequency data generally demonstrated a cyclical pattern. The smallest were collected in September and the largest in May. Post-hoc analysis showed no significant difference in length between August and May, or among the other months. In Volusia County (VC), annual monthly length-frequency distribution demonstrated growth generally occurred from late-winter and spring to summer. The smallest ladyfish were collected in February and the largest in August. On average, the absolute growth rate in the IRL was 36.3 mm in 60 days or 0.605 mm day−1. Cohort-specific daily growth rates, elevations, and coincidentals were similar among sampling years. Cohort-specific growth rates ranged from 1.807 in 1993 to 1.811 mm day−1in 1994. Overall, growth was best (i.e., goodness of fit) described by exponential regression. On average, the absolute growth rate in VC was 28 mm in 150 days or 0.1866 mm day−1. Cohort-specific daily growth rates were significantly different among sampling years; however, the elevations and coincidentals were similar. Cohort-specific growth rates ranged from 1.741 in 1994 to 1.933 mm day−1in 1993. Mean ladyfish growth was best described by linear regression; however, natural growth was explained better by exponential regression. In the IRL, the corrected exponential growth equation yielded a size-at-age 1 of 156.0 mm SL, which corresponded to an estimated growth rate of 0.4356 mm day−1. In VC, the corrected exponential growth equation yielded a size-at-age 1 of 80 mm SL corresponding to an estimated growth rate of 0.2361 mm day−1.

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.

scholarly journals Age, growth, and recruitment patterns of juvenile ladyfish (Elops sp) from the east coast of Florida (USA)

2015 ◽  
Author(s):  
Juan C Levesque
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Age And Growth ◽  
Growth Equation ◽  
Length Frequency ◽  
Daily Growth ◽  
Exponential Regression ◽  
Absolute Growth ◽  
Specific Growth Rates ◽  
Size At Age

Ladyfish (Elops sp) are a common and economically valuable coastal nearshore species found along coastal beaches, bays, and estuaries of the southeastern United States, and subtropical and tropical regions worldwide. Previously, ladyfish were a substantial bycatch in Florida’s commercial fisheries, but changes in regulations significantly reduced commercial landings. Today, ladyfish are still taken in commercial fisheries in Florida, but many are also taken by recreational anglers. Life-history information and research interest in ladyfish is almost non-existent, especially information on age and growth. Thus, the overarching purpose of this study was to expand our understanding of ladyfish age and growth characteristics. The specific objectives were to describe, for the first time, age, growth, and recruitment patterns of juvenile ladyfish from the east coast of Florida (USA). In the Indian River Lagoon (IRL), annual monthly length-frequency distributions were confounded because a few small individuals recruited throughout the year; monthly length-frequency data generally demonstrated a cyclical pattern. The smallest were collected in September and the largest in May. Post-hoc analysis showed no significant difference in length between August and May, or among the other months. In Volusia County (VC), annual monthly length-frequency distribution demonstrated growth generally occurred from late-winter and spring to summer. The smallest ladyfish were collected in February and the largest in August. On average, the absolute growth rate in the IRL was 36.3 mm in 60 days or 0.605 mm day-1. Cohort-specific daily growth rates, elevations, and coincidentals were similar among sampling years. Cohort-specific growth rates ranged from 1.807 in 1993 to 1.811 mm day-1 in 1994. Overall, growth was best (i.e., goodness of fit) described by exponential regression. On average, the absolute growth rate in VC was 28 mm in 150 days or 0.1866 mm day-1. Cohort-specific daily growth rates were significantly different among sampling years; however, the elevations and coincidentals were similar. Cohort-specific growth rates ranged from 1.741 in 1994 to 1.933 mm day-1 in 1993. Mean ladyfish growth was best described by linear regression; however, natural growth was explained better by exponential regression. In the IRL, the corrected exponential growth equation yielded a size-at-age 1 of 156.0 mm SL, which corresponded to an estimated growth rate of 0.4356 mm day-1. In VC, the corrected exponential growth equation yielded a size-at-age 1 of 80 mm SL corresponding to an estimated growth rate of 0.2361 mm day-1.

scholarly journals Age, growth, and recruitment patterns of juvenile ladyfish (Elops sp) from the east coast of Florida (USA)

2015 ◽  
Author(s):  
Juan C Levesque
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Age And Growth ◽  
Growth Equation ◽  
Length Frequency ◽  
Daily Growth ◽  
Exponential Regression ◽  
Absolute Growth ◽  
Specific Growth Rates ◽  
Size At Age

Ladyfish (Elops sp) are a common and economically valuable coastal nearshore species found along coastal beaches, bays, and estuaries of the southeastern United States, and subtropical and tropical regions worldwide. Previously, ladyfish were a substantial bycatch in Florida’s commercial fisheries, but changes in regulations significantly reduced commercial landings. Today, ladyfish are still taken in commercial fisheries in Florida, but many are also taken by recreational anglers. Life-history information and research interest in ladyfish is almost non-existent, especially information on age and growth. Thus, the overarching purpose of this study was to expand our understanding of ladyfish age and growth characteristics. The specific objectives were to describe, for the first time, age, growth, and recruitment patterns of juvenile ladyfish from the east coast of Florida (USA). In the Indian River Lagoon (IRL), annual monthly length-frequency distributions were confounded because a few small individuals recruited throughout the year; monthly length-frequency data generally demonstrated a cyclical pattern. The smallest were collected in September and the largest in May. Post-hoc analysis showed no significant difference in length between August and May, or among the other months. In Volusia County (VC), annual monthly length-frequency distribution demonstrated growth generally occurred from late-winter and spring to summer. The smallest ladyfish were collected in February and the largest in August. On average, the absolute growth rate in the IRL was 36.3 mm in 60 days or 0.605 mm day-1. Cohort-specific daily growth rates, elevations, and coincidentals were similar among sampling years. Cohort-specific growth rates ranged from 1.807 in 1993 to 1.811 mm day-1 in 1994. Overall, growth was best (i.e., goodness of fit) described by exponential regression. On average, the absolute growth rate in VC was 28 mm in 150 days or 0.1866 mm day-1. Cohort-specific daily growth rates were significantly different among sampling years; however, the elevations and coincidentals were similar. Cohort-specific growth rates ranged from 1.741 in 1994 to 1.933 mm day-1 in 1993. Mean ladyfish growth was best described by linear regression; however, natural growth was explained better by exponential regression. In the IRL, the corrected exponential growth equation yielded a size-at-age 1 of 156.0 mm SL, which corresponded to an estimated growth rate of 0.4356 mm day-1. In VC, the corrected exponential growth equation yielded a size-at-age 1 of 80 mm SL corresponding to an estimated growth rate of 0.2361 mm day-1.

Genotypic differences in seed growth rates of Phaseolus vulgaris L. I. General characteristics, seed coat factors and comparative roles of seed coats and cotyledons

2000 ◽  
Vol 27 (2) ◽  
pp. 109 ◽  
Author(s):  
Melinda Thomas ◽  
Louise Hetherington ◽  
John W. Patrick
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Dry Matter ◽  
Cultivar Differences ◽  
Phaseolus Vulgaris L ◽  
Surface Areas ◽  
Parenchyma Cells ◽  
Absolute Growth ◽  
Cultivar Variation ◽  
Seed Coats

Developing seeds of four cultivars of Phaseolus vulgaris L., raised under glasshouse conditions, exhib-ited a 4-fold range in rates of storage product accumulation by their cotyledons. These growth rate differences were established during seed expansion. Patterns of dry matter distribution were consistent with absolute growth rates of cotyledons being an inherent property of developing seeds and not limited by photoassimilate supply. Seed surface areas and cotyledon volumes exhibited a 3.2-fold cultivar difference and were the principal components contribut-ing to cultivar variation in cotyledon absolute growth rates. The remaining cultivar variation was attributable to a 1.3- fold difference in dry matter fluxes, expressed on a seed surface area basis. Seed coats reflected these properties in terms of fluxes of dry matter released for cotyledon storage and surface areas supporting these fluxes. Seed coat surface areas correlated with estimates of total plasma membrane areas of ground parenchyma cells that are respon-sible for photoassimilate release. Cultivar differences in these membrane areas largely arose from variation in cell size. Coat turgor pressures correlated positively with dry matter fluxes imported into cotyledons. In contrast, sucrose concentration in bulk saps extracted from seed coats was identical across three cultivars but was positively related to growth rate in the remaining cultivar. Overall, these data suggested that cultivar dry matter fluxes were determined by variation in transport conductances for symplasmic movement through the post-sieve element pathway and for release across the plasma membranes of ground parenchyma cells. Comparable sucrose concentrations were found in seed apoplasmic saps across cultivars, and cultivar differences in absolute growth rates of in vitro cultured coty-ledons were retained. Together, these observations support the conclusion that cotyledons intrinsically express geno-typic variation in rates of dry matter transport comparable to those set independently by seed coats.

scholarly journals Resistance of a lowland rain forest to increasing drought intensity in Sabah, Borneo

2004 ◽  
Vol 20 (6) ◽  
pp. 613-624 ◽  
Author(s):  
D. M. Newbery ◽  
M. Lingenfelder
Keyword(s):  
Growth Rates ◽  
Rain Forest ◽  
Tree Mortality ◽  
Mortality Rates ◽  
Stem Growth ◽  
Lowland Rain Forest ◽  
Drought Intensity ◽  
Tree Survival ◽  
Climatic Environment ◽  
Absolute Growth

Occasional strong droughts are an important feature of the climatic environment of tropical rain forest in much of Borneo. This paper compares the response of a lowland dipterocarp forest at Danum, Sabah, in a period of low (LDI) and a period of high (HDI) drought intensity (1986–96, 9.98 y; 1996–99, 2.62 y). Mean annual drought intensity was two-fold higher in the HDI than LDI period (1997 v. 976 mm), and each period had one moderately strong main drought (viz. 1992, 1998). Mortality of ‘all’ trees ≥10 cm gbh (girth at breast height) and stem growth rates of ‘small’ trees 10–<50 cm gbh were measured in sixteen 0.16-ha subplots (half on ridge, half on lower slope sites) within two 4-ha plots. These 10–50-cm trees were composed largely of true understorey species. A new procedure was developed to correct for the effect of differences in length of census interval when comparing tree mortality rates. Mortality rates of small trees declined slightly but not significantly between the LDI and HDI periods (1.53 to 1.48% y−1): mortality of all trees showed a similar pattern. Relative growth rates declined significantly by 23% from LDI to HDI periods (11.1 to 8.6 mm m−1 y−1): for absolute growth rates the decrease was 28% (2.45 to 1.77 mm y−1). Neither mortality nor growth rates were significantly influenced by topography. For small trees, across subplots, absolute growth rate was positively correlated in the LDI period, but negatively correlated in the HDI period, with mortality rate. There was no consistent pattern in the responses among the 19 most abundant species (n≥50 trees) which included a proposed drought-tolerant guild. In terms of tree survival, the forest at Danum was resistant to increasing drought intensity, but showed decreased stem growth attributable to increasing water stress.

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

Placental restriction of fetal growth reduces size at birth and alters postnatal growth, feeding activity, and adiposity in the young lamb

2007 ◽  
Vol 292 (2) ◽  
pp. R875-R886 ◽  
Author(s):  
Miles J. De Blasio ◽  
Kathryn L. Gatford ◽  
Jeffrey S. Robinson ◽  
Julie A. Owens
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Feeding Activity ◽  
Later Life ◽  
Postnatal Growth ◽  
Postnatal Life ◽  
Absolute Growth ◽  
Accelerated Growth ◽  
Early Postnatal Life ◽  
Size At Birth

Intrauterine growth restriction (IUGR) is associated with accelerated growth after birth. Together, IUGR and accelerated growth after birth predict reduced lean tissue mass and increased obesity in later life. Although placental insufficiency is a major cause of IUGR, whether it alters growth and adiposity in early postnatal life is not known. We hypothesized that placental restriction (PR) in the sheep would reduce size at birth and increase postnatal growth rate, fat mass, and feeding activity in the young lamb. PR reduced survival rate and size at birth, with soft tissues reduced to a greater extent than skeletal tissues and relative sparing of head width ( P < 0.05 for all). PR did not alter absolute growth rates (i.e., the slope of the line of best fit for age vs. parameter size from birth to 45 days of age) but increased neonatal fractional growth rates (absolute growth rate relative to size at birth) for body weight (+24%), tibia (+15%) and metatarsal (+18%) lengths, hindlimb (+23%) and abdominal (+19%) circumferences, and fractional growth rates for current weight ( P < 0.05) weekly throughout the first 45 days of life. PR and small size at birth reduced individual skeletal muscle weights and increased visceral adiposity in absolute and relative terms. PR also altered feeding activity, which increased with decreasing size at birth and was predictive of increased postnatal growth and adiposity. In conclusion, PR reduced size at birth and induced catch-up growth postnatally, normalizing weight and length but increasing adiposity in early postnatal life. Increased feeding activity may contribute to these alterations in growth and body composition following prenatal restraint and, if they persist, may lead to adverse metabolic and cardiovascular outcomes in later life.

Comparative breed studies of beef cattle. I. Changes in body weight

1963 ◽  
Vol 14 (6) ◽  
pp. 882 ◽  
Author(s):  
NM Tulloh
Keyword(s):  
Body Weight ◽  
Growth Rates ◽  
The Other ◽  
Relative Growth ◽  
Relative Growth Rates ◽  
Breed Differences ◽  
Weaning Age ◽  
Absolute Growth ◽  
The Mean ◽  
One Year

A comparative growth study was made of Hereford, Aberdeen Angus, and beef Shorthorn cattle reared and kept together throughout their lives on irrigated perennial pastures at the Metropolitan Farm, Werribee, Vic. Records of body weight as a function of age were obtained on 404 Hereford, 172 Aberdeen Angus, and 127 Shorthorn cattle, representing cattle born in 1955, 1957, 1958, 1959, and 1960. At birth, male calves were significantly heavier than females, and Hereford calves were significantly heavier than Shorthorn and Aberdeen Angus calves, the birth weights of Shorthorn and Aberdeen Angus calves being similar. Up to the age of 5 years, the younger and lighter 2-year-old cows produced lighter calves than cows which were both older and heavier. At weaning age (9.5 months) steers were significantly heavier than heifers. Herefords were significantly heavier than Aberdeen Angus in two years out of three; and in one year out of three, Herefords were significantly heavier than Shorthorns. Shorthorns were significantly heavier than Aberdeen Angus in one year out of three. When the steers were finally weighed off grass at the mean age of either 20 months (1958, 1959, and 1960 cattle) or 25 months (1957 cattle), Herefords were significantly heavier than Aberdeen Angus in four successive years, and in one year out of four the Herefords were significantly heavier than Shorthorns. In three years out of four, Shorthorns were significantly heavier than Aberdeen Angus. Breed differences between the mean weights of breeding cows were not significant and, up to the age of 5 years, as breeding cows grew older they became heavier. Body weight growth curves indicated that the cattle experienced a severe check in growth during the winter months (June, July, August). At other times of the year, growth rates were satisfactory. Cattle born in some years grew better than cattle born in others. This was thought to be due partly to differences between years in the quality and quantity of pasture available, even though the pastures were irrigated. Average absolute and average relative growth rates were calculated for the 1957 and 1958 steers before and after weaning. Breed differences in absolute growth rates before weaning were not statistically significant, but after weaning, rates were significantly the highest for Herefords in both years. The breed differences in average relative growth rates were in the same direction as those for absolute growth rates. However, the pre-weaning relative growth rate of Shorthorns was significantly higher than those of the other breeds among the 1957 steers. When due allowance was made for the smaller size of Aberdeen Angus steers at birth and at weaning, the relative growth rates of this breed were less than those of the other breeds. Absolute and relative growth rates were higher for all breeds before weaning than afterwards. This was mainly a reflexion of low post-weaning growth rates during the winter months. Rank correlation coefficients between birth weight and weight at subsequent ages were low and variable in different breeds and in different seasons. However, coefficients calculated between subsequent ages, beginning at weaning age, were generally highly significant. The breed and sex differences presented in this paper have been compared with the limited data from the literature and, in general, the results are similar.

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