Relative Growth (relative + growth)

Distribution by Scientific Domains

Terms modified by Relative Growth

  • relative growth rate

  • Selected Abstracts


    Socioeconomic Prognosis after a Newly Diagnosed Unprovoked Epileptic Seizure in Adults: A Population-based Case,Control Study

    EPILEPSIA, Issue 10 2002
    Hans Lindsten
    Summary: , Purpose: To investigate the socioeconomic prognosis after a newly diagnosed unprovoked epileptic seizure in adults. Methods: Sixty-three patients 17 years or older with a newly diagnosed unprovoked epileptic seizure from 1985 through 1987 and 107 sex- and age- matched controls were followed up for 10 years to 1996. Studied variables were income, source of income, sickness periods, incapacity rate, diagnosis-specific incapacity rate, vocational status, and education. Results: Relative growth of income was similar between patients and controls during follow-up. Patients had lower income than did controls 2 years before seizure onset and during the entire follow-up. This was related to higher morbidity among patients, as measured by sickness periods and incapacity rate. Employment rates did not evolve negatively among patients after seizure onset and were close to employment rates of controls during follow-up time. There was no difference between patients and controls regarding education. Conclusions: After a newly diagnosed unprovoked epileptic seizure in adults, no negative development regarding employment and education occurs. Income development is positive unless refractory seizures evolve. However, income is lower among patients with epilepsy than among controls, and this difference can be related to overall morbidity. [source]


    Commercial-scale Validation of Temperature-step Rearing on Growth Physiology in Turbot, Scophthalmus maximus

    JOURNAL OF THE WORLD AQUACULTURE SOCIETY, Issue 5 2008
    Albert K. Imsland
    The aim of this study was to investigate the possible benefit of "temperature-steps" (T-steps) rearing for juvenile turbot (initial weight 15.1 g) under realistic production scale and to determine whether initial growth advantage is maintained throughout the rearing period to market size. One group (called T-step 22-19-16) of juvenile turbot was reared at three different temperatures, that is, 22 C (from 17 to 60 g) followed by 19 C (from 60 to 100 g) and 16 C (>100 g); another group (called T-step 19-16) at two temperatures, that is, 19 C (from 17 to 100 g) and lowered to 16 C (>100 g); and the third group (called C16) at one constant temperature, that is, 16 C. Relative growth was significantly higher in the two T-step groups, with the T-step 19-16 showing the highest overall growth. Feed conversion efficiency was highest in the 19-16 group. Only minor effects of the experimental rearing on blood physiology were found, with one notable exception of inverse relationship between plasma glucose and growth. Overall, these findings indicate that a short interval of rearing fish at high temperature during the early juvenile phase may have a long-term effect on biomass increment in turbot. This is an important finding for the turbot industry. [source]


    Size at the onset of sexual maturity in the anomuran crab, Aegla uruguayana (Aeglidae)

    ACTA ZOOLOGICA, Issue 4 2006
    Verónica E. Viau
    Abstract The size at maturity was studied in the crab Aegla uruguayana from the Areco River (31°14, S, 59°28, W), Argentina. Size at sexual maturity was determined according to three criteria: morphometric (change in the relative growth of reproductive characters), histological (first maturation of gonads) and functional (capability to mate and carry eggs). Regarding females, morphometric maturity occurred at a carapace length (CL) of 11.50 mm, considering abdomen width as a reproductive character. Gonad maturity of females could be observed at a minimum size ranging from 15 to 17 mm CL. The smallest ovigerous female observed in the field was 15.60 mm CL, although a relevant population incidence of ovigerous females (86.6%) has just been observed at values higher than 17 mm CL. As for males, the relative growth of the left chela length changed at a value of 15.40 mm CL, while morphological changes in sexual tube occurred between CL of 14 and 16 mm. Testicular maturation occurred at a CL ranging from 17 to 19 mm. The smallest size of males having spermatozoids in their vasa deferentia was 18.70 mm CL. The results obtained indicated that, in both sexes, functional maturity occurred after morphometric maturity and at a size similar to that of gonad maturity. Comparing sexes, females acquired sexual maturity (morphometric, gonad and functional maturity) at sizes statistically smaller than those of males. [source]


    English county populations in the later eighteenth century1

    ECONOMIC HISTORY REVIEW, Issue 1 2007
    E. A. WRIGLEY
    SUMMARY When directing the first English census John Rickman was intent not only on discovering the size of the population in 1801 but also on tracing past trends both nationally and for individual counties. He returned to the latter investigation on several later occasions, notably in the 1830s. There have been many subsequent attempts to improve upon his national estimates, but his estimates of county totals have continued to be used extensively, either unchanged or slightly modified. Rickman was aware that his estimates were subject to wide margins of error. For the later eighteenth century it is possible to produce new estimates which are probably substantially more accurate, taking advantage of the fact that after Hardwicke's Act (1753) the registration of marriages in Anglican parish registers, unlike that of baptisms and burials, was virtually complete. They show that the contrast between population growth rates in ,industrial' counties and those in which agriculture continued to predominate were significantly more marked than suggested by Rickman's estimates. The same exercise that produces county estimates also yields hundredal totals, which will in future allow a more refined account of relative growth and stagnation to be made. [source]


    Ontogenetic variability in external morphology of bighead goby Neogobius kessleri from the Middle Danube, Slovakia

    JOURNAL OF APPLIED ICHTHYOLOGY, Issue 4 2005
    V. Ková
    Summary Over the last decade, four species of goby have invaded the Middle Danube area, and all of them have spread rapidly. In the early 1990s, bighead goby Neogobius kessleri appeared in the Middle Danube, where it now seems to thrive. Relatively little is known of the environmental biology and ontogeny of this species in its native and non-native ranges. In this paper, preliminary results on the external morphology of bighead goby from the Slovak stretch of the Danube are presented within an ontogenetic context. Patterns of relative growth with no apparent changes at small size suggest direct development in bighead goby, although not as profoundly direct as observed in round goby N. melanostomus. Differences in life history between these two closely related species may have important implications for their success in novel environments, favouring the latter in short term (several years) and the former in long term (decades and longer) perspective. [source]


    Ontogenetic induced shifts in the ecology of sunbleak Leucaspius delineatus during early development

    JOURNAL OF FISH BIOLOGY, Issue 2005
    A. C. Pinder
    Using the non-native sunbleak Leucaspius delineatus as a model, the relationship between ontogeny and ecology was studied with a view to identifying specific morphological and physiological processes involved in influencing ecological niche shifts. Following a predefined saltatory model for the early ontogeny of sunbleak, field studies examined the temporal use of microhabitat, diet and morphological changes throughout early development. Following a dramatic shift in both morphology and ecology between the free embryo phase and the larval period, habitat use and diet showed little change during the larval period, with habitat use confined to marginal, vegetated areas and prey items associated with these habitats well represented in the diet. During the final larval step (L5), transition to the juvenile period resulted in the stabilization of relative growth, acquisition of the adult morphotype and was associated with a clear shift in diet and habitat use. During this period, sunbleak moved for the first time into open, deeper water, away from the banks, and utilized a similar range of food items to the adults. Specific relationships between form and function are further discussed. [source]


    Description and ontogeny of young Stolephorus baganensis and Thryssa kammalensis, two Engraulididae from Peninsular Malaysia

    JOURNAL OF FISH BIOLOGY, Issue 6 2000
    V. Sarpéadonti
    The morphology of the digestive system was useful to distinguish the larvae of Stolephorus baganensis and Thryssa kammalensis before the full development of their dorsal and anal fins. The relative positions of these fins, the length of the anal fin, and body depth, were good criteria for identifying individuals >10·0 mm LS. For both species, the relative growth of the ten morphometric characters studied was best explained by linear piecewise regressions indicating inflection in allometry at specific standard lengths. Most of these sudden changes in growth rate occurred between 6·9 and 10·0 mm LS for S. baganensis and between 5·8 and 8·9 mm LS for T. kammalensis. Double-centred principal component analysis (PCA) confirmed important changes in the external morphology of both species during this transition period. Prior to this period, the main parameters characterizing the global morphological changes of both species were the length and position of dorsal and anal fins whereas they were body depth and eye diameter (only in S. baganensis) for larger specimens. Complete development of scales did not appear as a suitable criterion to define the end of the larval period, which, instead, was set at the size at which larvae presented an adult-like pigmentation (respectively 35·0 mm LS and 55·0 mm LS in S. baganensis and T. kammalensis). [source]


    Mathematical modeling of appendicular bone growth in glaucous-winged gulls

    JOURNAL OF MORPHOLOGY, Issue 1 2009
    James L. Hayward
    Abstract Development of locomotor activity is crucial in tetrapods. In birds, this development leads to different functions for hindlimbs and forelimbs. The emergence of walking and flying as very different complex behavior patterns only weeks after hatching provides an interesting case study in animal development. We measured the diaphyseal lengths and midshaft diameters of three wing bones (humerus, ulna, and carpometacarpus) and three leg bones (femur, tibiotarsus, and tarsometatarsus) of 79 juvenile (ages 0,42 days) and 13 adult glaucous-winged gulls (Larus glaucescens), a semiprecocial species. From a suite of nine alternative mathematical models, we used information-theoretic criteria to determine the best model(s) for length and diameter of each bone as a function of age; that is, we determined the model(s) that obtained the best tradeoff between the minimized sum of squared residuals and the number of parameters used to fit the model. The Janoschek and Holling III models best described bone growth, with at least one of these models yielding an R2 , 0.94 for every dimension except tarsometatarsus diameter (R2 = 0.87). We used the best growth models to construct accurate allometric comparisons of the bones. Early maximal absolute growth rates characterize the humerus, femur, and tarsometatarsus, bones that assume adult-type support functions relatively early during juvenile development. Leg bone lengths exhibit more rapid but less sustained relative growth than wing bone lengths. Wing bone diameters are initially smaller than leg bone diameters, although this relationship is reversed by fledging. Wing bones and the femur approach adult length by fledging but continue to increase in diameter past fledging; the tibiotarsus and tarsometatarsus approach both adult length and diameter by fledging. In short, the pattern of bone growth in this semiprecocial species reflects the changing behavioral needs of the developing organism. J. Morphol., 2009. © 2008 Wiley-Liss, Inc. [source]


    Manipulation of crystal shape by cycles of growth and dissolution

    AICHE JOURNAL, Issue 6 2007
    Ryan C. Snyder
    Abstract A method for the manipulation of crystal shape by using cycles of growth and dissolution is presented, representing a unique process-based solution to an important product quality concern. Using 3-D shape evolution models for faceted crystal growth and dissolution, results are reported for cycling both an illustrative crystal system, as well as a physical plate-like system. The results show that crystal shape can be manipulated by cycling when the relative growth and dissolution rates are anisotropic, which can be caused by differences in growth mechanism, asymmetry in super/undersaturation, and by the use of surface active additives. Since this method of crystal shape enhancement uses the existing liquid solution, it could be a valuable alternative to the traditional methods which often require changes in the chemical nature of the solution, for example, by changing solvent. © 2007 American Institute of Chemical Engineers AIChE J, 2007 [source]


    Ontogeny and phyletic size change in living and fossil lemurs

    AMERICAN JOURNAL OF PRIMATOLOGY, Issue 2 2010
    Matthew J. Ravosa
    Abstract Lemurs are notable for encompassing the range of body-size variation for all primates past and present,close to four orders of magnitude. Benefiting from the phylogenetic proximity of subfossil lemurs to smaller-bodied living forms, we employ allometric data from the skull to probe the ontogenetic bases of size differentiation and morphological diversity across these clades. Building upon prior pairwise comparisons between sister taxa, we performed the first clade-wide analyses of craniomandibular growth allometries in 359 specimens from 10 lemuroids and 176 specimens from 8 indrioids. Ontogenetic trajectories for extant forms were used as a criterion of subtraction to evaluate morphological variation, and putative adaptations among sister taxa. In other words, do species-level differences in skull form result from the differential extension of common patterns of relative growth? In lemuroids, a pervasive pattern of ontogenetic scaling is observed for facial dimensions in all genera, with three genera also sharing relative growth trajectories for jaw proportions (Lemur, Eulemur, Varecia). Differences in masticatory growth and form characterizing Hapalemur and fossil Pachylemur likely reflect dietary factors. Pervasive ontogenetic scaling characterizes the facial skull in extant Indri, Avahi, and Propithecus, as well as their larger, extinct sister taxa Mesopropithecus and Babakotia. Significant interspecific differences are observed in the allometry of indrioid masticatory proportions, with variation in the mechanical advantage of the jaw adductors and stress-resisting elements correlated with diet. As the growth series and adult data are largely coincidental in each clade, interspecific variation in facial form may result from selection for body-size differentiation among sister taxa. Those cases where trajectories are discordant identify potential dietary adaptations linked to variation in masticatory forces during chewing and biting. Although such dissociations highlight selection to uncouple shared ancestral growth patterns, they occur largely via transpositions and retention of primitive size-shape covariation patterns or relative growth coefficients. Am. J. Primatol. 72:161,172, 2010. © 2009 Wiley-Liss, Inc. [source]


    Repeat Organ Transplantation in the United States, 1996,2005

    AMERICAN JOURNAL OF TRANSPLANTATION, Issue 2007
    J. C. Magee
    The prospect of graft loss is a problem faced by all transplant recipients, and retransplantation is often an option when loss occurs. To assess current trends in retransplantation, we analyzed data for retransplant candidates and recipients over the last 10 years, as well as current outcomes. During 2005, retransplant candidates represented 13.5%, 7.9%, 4.1% and 5.5% of all newly registered kidney, liver, heart and lung candidates, respectively. At the end of 2005, candidates for retransplantation accounted for 15.3% of kidney transplant candidates, and lower proportions of liver (5.1%), heart (5.3%) and lung (3.3%) candidates. Retransplants represented 12.4% of kidney, 9.0% of liver, 4.7% of heart and 5.3% of lung transplants performed in 2005. The absolute number of retransplants has grown most notably in kidney transplantation, increasing 40% over the last 10 years; the relative growth of retransplantation was most marked in heart and lung transplantation, increasing 66% and 217%, respectively. The growth of liver retransplantation was only 11%. Unadjusted graft survival remains significantly lower after retransplantation in the most recent cohorts analyzed. Even with careful case mix adjustments, the risk of graft failure following retransplantation is significantly higher than that observed for primary transplants. [source]