PATTERNS OF GROWTH IN BIRDS

Parameters used to characterize the course of growth are described, and calculated growth parameters are presented for 105 species of birds of many taxonomic groups from a wide range of geographical localities. Growth parameters are found to exhibit as much as 20% variation within a species with respect to geographic locality and time of the nesting season. There is also considerable local variation, irrespective of season and locality, which is related to nutrition and perhaps to an inherited variability. The application of curve-fitting as a method of analysing intraspecific variation is discussed briefly, and the importance of comparative growth studies is emphasized. Growth patterns are correlated with other parameters of the life-history to evaluate the extent of diversity in the course of growth. Low rates of growth and prolonged growth periods occur primarily in species large for their families and in oceanic species. In most others, high rates of growth are maintained for longer periods of time. The shape of the growth curve is not related to the mode of development (i.e. whether precocial or altricial). Overall relative, or weight-specific growth rates, as measured by the constants of fitted growth equations, are most highly correlated with the adult body size of the species, changing as the -0–278 power of adult body weight. Smaller variations in the rate of growth appear to be correlated with differences in nesting success; open-nesting passerines grow faster than hole-nesting species of a similar size. Growth rate is further correlated with brood size. Oceanic species with single egg clutches and tropical land-birds with small clutches have low growth rates. The asymptote of the growth curve of the young (in relation to the adult weight) is related to the foraging behaviour of the adults. Aerial feeders generally have high asymptotes while those of ground feeding species are usually below adult weight. These differences are related to the need in the former for well-developed flight at the time of fledging. The diversity of growth patterns is related to evolutionary trends which are the result of (1) selective forces acting at stages of the life-history cycle other than development, (2) factors which affect the survival of offspring during the growth period, and (3) adjustments made to balance the energy budget of the family group. The last trend is discussed in detail in relation to the correlations found in the analysis. Two hypotheses are presented. Firstly, in species which cannot gather enough food to support even one young at a normal growth rate, the pace of development is reduced to decrease the energetic requirements of the young. Secondly, in species with small clutches, where adjustments to feeding capacities are not readily made by changing brood size, growth rate may be adjusted to accomplish this. The lack of critical energetic data to test these hypotheses is emphasized as a major deficiency in our understanding of the breeding biology of birds.     

HIGH RATES OF EVOLUTION PRECEDED THE ORIGIN OF BIRDS

The origin of birds (Aves) is one of the great evolutionary transitions. Fossils show that many unique morphological features of modern birds, such as feathers, reduction in body size, and the semilunate carpal, long preceded the origin of clade Aves, but some may be unique to Aves, such as relative elongation of the forelimb. We study the evolution of body size and forelimb length across the phylogeny of coelurosaurian theropods and Mesozoic Aves. Using recently developed phylogenetic comparative methods, we find an increase in rates of body size and body size dependent forelimb evolution leading to small body size relative to forelimb length in Paraves, the wider clade comprising Aves and Deinonychosauria. The high evolutionary rates arose primarily from a reduction in body size, as there were no increased rates of forelimb evolution. In line with a recent study, we find evidence that Aves appear to have a unique relationship between body size and forelimb dimensions. Traits associated with Aves evolved before their origin, at high rates, and support the notion that numerous lineages of paravians were experimenting with different modes of flight through the Late Jurassic and Early Cretaceous.     

LEAF INITIATION RATES AND VOLUME GROWTH RATES IN THE SHOOT APEX OF CHRYSANTHEMUM

The leaf initiation rate and apical volume growth rate of lateral shoots of Chrysanthemum morifolium ‘Improved Albatross III’ were determined for plants growing under controlled environment conditions. After removal of the terminal bud, the top two lateral buds produced leaves at a rate of 1.4 to 1.6 leaves/day for the first 9 or 10 days. At about the 10th day there appeared to be an abrupt shift to a lower initiation rate of 0.7 to 0.8 leaves/day. Defoliation by periodic removal of leaves larger than 1 cm caused a statistically significant increase in initiation rate, but not to as high a rate as that of the first 10 days of bud growth. Volume growth rates of the apical region were determined from transverse sections of five apices, according to the method of Richards (1951). The apical region was found to have a radial expansion rate of 0.1623/plastochron and a vertical expansion rate of 0.0494/plastochron. The volume growth rate was calculated to be 0.3740/plastochron and the volume doubling time to be 1.85 plastochrons or 56 to 63 hr.     

鸟类生长发育研究方面的某些进展

本文将近20年来鸟类生长发育的研究状况分4个方面作了概述。首先介绍了雏鸟体重增长的几种模型;其次概括地分析了影响鸟类生长率的几种重要因素以及雏鸟身体结构中,不同部位的生长与发育的关系;最后讨论了控制生长发育的几种假设。     

PATTERNS OF GROWTH IN BIRDS. II. GROWTH RATE AND MODE OF DEVELOPMENT

This analysis was initiated to examine the relationship between the rate of growth in birds and their development of mature function. The literature was surveyed for data on growth and development, and the growth curves of 81 species were chosen for the analysis. Growth curves of most species were fitted with the Gompertz equation, and the rate constants of the equation were used as an index of the growth rate. For those species whose curves were fitted better by other equations, with a slightly different form, appropriate conversion factors, derived in this paper, were employed.
Among species with similar modes of development, growth rate decreases with increasing body weight in an allometric manner, with slopes of –0.26 to –0.42, depending on the group. Between groups, the rate of growth in body weight was found to be closely associated with the rate of development of function, in particular, the acquisition of flight. Among those species that can walk at an early age, but acquire flight relatively late, the rate of growth depends primarily on the relative size of the musculature of the lower extremities.
Data are presented to refute the hypotheses that growth rate is adjusted to nestling mortality, or that the energy requirements of the young (and hence their growth rates) are balanced against brood size. It is concluded that most species grow at some physiologically maximum rate, but as yet it is not possible to distinguish between limitation of growth rate at the level of the organism or at the level of the tissue.     

THE EFFECTS OF LIGHT AND TEMPERATURE ON GROWTH RATES IN BOREAL-SUBARCTIC CRUSTOSE CORALLINES1

A number of boreal-subarctic crustose corallines were kept in natural seawater tanks at temperatures ranging from 0 to 19 C and, using fluorescent lamps at light intensities, ranging from 7 to 750 lux with periods of 8 and 14 hr/day. The resultant growth rates as a function of temperature and light are presented and discussed in relation to the ecology of the plants. All of the Lithothamnieae studied had growth maxima at temperatures from 9 to 15 C. Growth in these species showed little light dependence below 4–6 C, but had a strong light dependence at higher temperatures. The one Lithophyllum species examined gave a flatter growth-temperature curve than the Lithothamnieae and showed little light dependence. The effects of temperature variation, salinity, and current on growth rates were also examined and are discussed. It was found to be especially important in studying growth rates of crustose corallines to allow time for growth stabilization following temperature change. In general, growth was found to exhibit a hysteresis effect, increased rates with the raising of temperatures 5–10 C and decreased rates with lowering temperatures.