Estimation of body weights from craniometric variables in baboons

Body weights of adult baboons (genera Papio, Mandrillus, and Theropithecus) were gathered from notes of collectors and museum records. However, these data were insufficient to establish mean body weights for all baboon groups. Thus, log cube roots of mean body weights were regressed as functions of the logs of several cranial and dental variables. The resulting least squares regression coefficients were used to estimate weights for 503 adult baboons from cranial measurements. The ability of the various regression functions to assess baboon body weight was determined by comparing reported and estimated mean and individual body weights. The best estimator of baboon body weights was the function derived from the factor scores of a principal components analysis of seven craniometric variables regressed on body weight. However, each of these craniometric variables singly was nearly as precise an estimator of body weight as the multivariate combination of all seven. Other measurements such as dental dimensions and foramen magnum area estimated weight less accurately. Body weight estimates derived from the regression analyses coupled with museum and literature records allowed an assessment of size relationships among all baboon groups.     

Red muscle fibre and capillary dimensions in different sizes of a tilapia, Oreochromis niloticus (Trewavas)

Measurements of muscle dimensions that affect respiration in relation to body weight were carried out in a tilapia, Oreochromis niloticus . The fish used in all measurements weighed 0.65–812.3 g. The data were analysed with respect to body weight using logarithmic transformations (log Y=log a + b log W ).
The slopes (b) of the log/log regression lines for weight of body trunk red muscle, average cross-sectional area of muscle fibre, average number of capillaries in direct contact with a muscle fibre, average capillary contact length with a fibre as a fraction of average fibre circumference and number of capillaries mm² of fibre cross-sectional area [N_A(cƒ)] were 1.16, 0.221, 0.084, 0.015, and −0.137 respectively.
These results show that there is an increase in muscle cross-sectional fibre area and number of capillaries in contact with muscle fibres whereas number of capillaries supplying a unit area of muscle fibre decreases during development. There is development of new capillaries with increase in cross-sectional area of red muscle fibres.     

Does the energy equivalence rule apply to intertidal macrobenthic communities?

Energy equivalence assumes equal contribution of large and small species to production and energy flow in communities. As in a double logarithmic plot, physiological rates decline with body weight by –0.25, log biomass should increase by 0.25 and log abundance decline by –0.75 with log species weight, when this concept is valid. This was tested with annual data sets of the macrobenthos of 4 intertidal sites in the German Wadden Sea (Königshafen) and 3 sites in a south Portuguese lagoon (Ria Formosa). Only abundance data from two of these sites displayed significantly negative slopes with mean body size of the species. Biomass and secondary production data were significantly positively correlated with mean body size for all Ria Formosa sites and also for the biomass of a mussel bed in Königshafen. However, high variation in body size of the individuals of a species limits interpretation of these plots.It is preferable to test this concept by body weight classes regardless of its species composition. At Königshafen, biomass and production displayed two distinct peaks. One peak at small body size was caused by browsing species. The other peak at larger body size was caused by animals which potentially extract their food from the water column. This bimodality was only vaguely reflected at one station in the Ria Formosa, possibly because of a dominance of detritus feeding species. In a normalized form (log biomass or production / width of size classvs. log size class), these spectra imply a dominance of small individuals in biomass and production at all sites (except for a mussel bank at Königshafen). This is interpreted as a consequence of permanent disturbances.     

Evolutionary dynamics of vertebrate body mass range

Change in body mass with time has been considered for many clades, often with reference to Cope's rule, which predicts a tendency to increase in body size. A more general rule, namely increase in the range of body mass with time, is analyzed here for vertebrates. The log range of log vertebrate body mass is shown to increase linearly and highly significantly with the log of duration of clade existence. The resulting regression equations are used to predict the origin age, initial body mass, and subsequent dynamics of body mass range for primate clades such as the New World monkeys (Platyrrhini, 32 million years ago, initial mass of 1.7 kg) and the Anthropoidea (57 million years ago, initial mass of 0.12 kg), tested against the primate fossil record. Using these methods, other major primate clades such as Lemuriformes and Adapoidea are also estimated to have originated in the Tertiary (63 and 64 million years ago, respectively), with only the Plesiadapiformes originating in the Cretaceous (83 million years ago). Similarities of body mass range between primate and other vertebrate sister groups are discussed. Linear relationships of log range and log duration are considered with respect to Brownian processes, with the expected regression coefficients from the latter explored through simulations. The observed data produce regression coefficients that overlap with or are higher than those under Brownian processes. Overall, the analyses suggest the dynamics of vertebrate body mass range in morphologically disparate clades are highly predictable over many tens of million years and that the dynamics of phenotypic characteristics can assist molecular clock and fossil models in dating evolutionary events.     

Growth of the African elephant (Loxodonta africana)

The three-stage desk calculation of the von Bertalanffy equation to describe growth in height and weight with age in the elephant is compared with a new approach to calculating the three coefficients in the function by a computer. The two methods give different results with respect to the weight/age calculations. Theoretical von Bertalanffy equations calculated by both methods to describe growth in height and weight with age in the African elephant in Zambia are compared with previously published equations for the elephant in East Africa. Details are given of growth in height in two known-age African elephants, a female ‘Diksie’ and a male ‘Kartoum’. Theoretical growth in height curves for the female African and Asiatic elephant are compared. The coefficients K and / for growth in height are not transferable to the growth in weight equations. Inherent inaccuracies in the calculation of the coefficients in the von Bertalanffy equation are discussed, and it is concluded that in animals which have a long life-span such as the elephant, the equation serves as a purely empirical representation of weight-at-age data and that there is little biological significance in the parameters it contains. The computer-calculated curves give the best fit to the data. The regression of log age on log shoulder height from 2–20 years of age provides a more realistic approach to comparative growth studies. The increase in adrenal weight with age is linear. Tusk growth in relation to age and sex in Zambia is compared with East Africa. It is concluded that the tusks in Zambia are smaller and are more difficult to sex correctly than their East African counterparts, possibly a consequence of the Zambian elephant having a greater degree of tusk wear. Allometric growth is described with emphasis on the estimation of body weight from shoulder height. The most reliable estimates are obtained from a purely empirical representation of the data, a semilog plot of log body weight on shoulder height.     

Protein-sodium dodecyl sulfate complexes: determination of molecular weight, size and shape by controlled pore glass chromatography

The peak position vs log molecular weight curves of protein-SDS complexes chromatographed on controlled pore glass of narrow pore size distribution is linear over a molecular weight range of 17,000–385,000. A glass with a pore size of approximately 500 Å allows the inclusion of all complexes in this range. Peak position curves on glasses with broad pore distributions show decreased resolution and deviate from linearity at low elution coefficients.Exclusion size analysis of the elution coefficients of individual complexes from different columns with pore diameters ranging from 197 to 650 Å gives from 120 to 423 Å as their longest dimension. Assuming constant hydration and SDS-to-protein ration, the found dimension suggests the shape of a football, rather than a sphere or rigid rod.     

How Big Is It Really? Assessing the Efficacy of Indirect Estimates of Body Size in Asian Elephants

Information on an organism’s body size is pivotal in understanding its life history and fitness, as well as helping inform conservation measures. However, for many species, particularly large-bodied wild animals, taking accurate body size measurements can be a challenge. Various means to estimate body size have been employed, from more direct methods such as using photogrammetry to obtain height or length measurements, to indirect prediction of weight using other body morphometrics or even the size of dung boli. It is often unclear how accurate these measures are because they cannot be compared to objective measures. Here, we investigate how well existing estimation equations predict the actual body weight of Asian elephants Elephas maximus, using body measurements (height, chest girth, length, foot circumference and neck circumference) taken directly from a large population of semi-captive animals in Myanmar (n = 404). We then define new and better fitting formulas to predict body weight in Myanmar elephants from these readily available measures. We also investigate whether the important parameters height and chest girth can be estimated from photographs (n = 151). Our results show considerable variation in the ability of existing estimation equations to predict weight, and that the equations proposed in this paper predict weight better in almost all circumstances. We also find that measurements from standardised photographs reflect body height and chest girth after applying minor adjustments. Our results have implications for size estimation of large wild animals in the field, as well as for management in captive settings.     

The ingestion in wolf spiders I. Capacity of gut ofLycosa pseudoannulata

An wolf spider, Lycosa pseudoannulata, collected from the field were reared in test tubes supplied with fruit flies as the food, and the number and weight of fruit flies killed per unit time and the weight of residuum of killed flies were recorded. When the cumulative number of flies killed by a spider was plotted against time after the beginning of food supply, the angle of the curve obtained decreased gradually until a constant value. In this time, it seems that the gut of spider had saturated with food and the increase rate of number of flies killed reflects the rate of food disappeared from gut by assimilation and egestion. The amount of ingestion was obtained by subtracting the weight of residuum and the gain of live weight of the spider from the weight of killed flies. After the gut has saturated, the amount of food remained in the gut is considered to be equal to the capacity of gut, which is an essential factor in the study of predation. The amount of food disappearance from gut was also estimated. There was a linear relationship between the log body weight of spiders and the log capacity of gut. The linear relationship was also seen between the log total amount of ingestion and the log total amount of food disappeared from gut.     

Variation in offspring size within a population of the web-building spiderAgelena limbata

Within a population of the web-building spiderAgelena limbata, the weight of the first instar nymphs ranged from 1.187 to 6.559 mg. Both intraclutch and interclutch variation were recorded. The mean weights were different among clutches and the coefficients of variation within a clutch ranged from 3.3 to 29.2%. Variation in the nymphal weight was certainly derived from variation in the egg weight because there was a high correlation between the two weights. Factors affecting interclutch variation in nymphal weight were examined by multiple regression analysis. Nymphal weight was positively correlated with the body size and food conditions of female parents, and negatively correlated with the clutch size. Among these three factors, the food conditions of female parents had the largest apparent effect on the interclutch variation. The results suggest that females with larger body size and more food produce larger offspring, and that there is a trade-off between offspring size and clutch size. Heavier nymphs had larger body size (carapace width) and may have larger energy reserves. Heavier nymphs survived experimental starvation for a significantly longer period.     

Allometry of gill dimensions in some British and American decapod crustacea

The gill areas and their component measurements of 16 species of North American crab and seven species of British decapod crustaceans have been analysed in relation to body mass using the method of logarithmic transformation.
A wide range of relationships was found, each of which is typical for a given species. The slope, b , of the log/log regression lines varied from 0·5 to 1·0, the lower values being most commonly found in the Macrura. For the North American species the average slope is about 0·8 whereas for British brachyurans the relationship was close to linear (b=0·97).
The analysis shows that the increase in gill surface body size is mainly due to the increasing area for individual platelets or gill lamellae.
Comparison of weight-specific gill areas for animals of the same body weight suggests that the most active species have larger gill areas. For some of these species the values (900mm²/g) approximate to those of active fish.
As plots for interspecific relationships derived from average values for many individual species have slopes which are not typical for any of the component species, it is concluded that caution must be exercized when interpreting such interspecific plots in Allometric studies.     

Echocardiographic parameters and indices in the normal beagle dog.

M-mode and two-dimensional echocardiographic measurements were made from the right sternal border of 50 healthy Beagles (25 males and 25 females) approximately 7 months old. The dogs were conscious and standing during the investigation. The following parameters, in systole and diastole, were measured on the echocardiographic images: left ventricular posterior wall thickness (LVWT); intraventricular septum thickness (IST); left ventricular internal dimension (LVID); and circumference (LVC). Fractional shortening (FS) and ejection fraction (EF) were also calculated. Mean, standard deviation, range and coefficient of variation are reported for each echocardiographic parameter and for body weight. Males and females were considered separately and together. Each parameter was analysed statistically to check for differences between the sexes and for correlations with body weight. A statistically significant difference between the sexes was only observed for LVWT in systole and diastole. A linear regression with body weight was obtained only for LVID in systole and in diastole. The results show that morphofunctional cardiac homogeneity is independent of size in dogs of this breed and age.     

Body Weight and Relative Brain Size (Encephalization) in Eocene Archaeoceti (Cetacea)

Calibration of the Brownian diffusion model of Felsenstein indicates that phylogeny may have an influence on body length and other phenotypic measures in Cetacea for as many as 10,000 generations or about 180,000 years, which is negligible in the 35 million year history of extant Cetacea. Observations of phenotypic traits in cetacean species living today are independent of phylogeny and independent statistically. Four methods for estimating body weight in fossil cetaceans are compared: (1) median serial regression involving a set of multiple regressions of log body weight on log centrum length, width, and height for core vertebrae; (2) regression of log whole body weight on log body length for individuals; (3) regression of log whole body weight on log body length for species means; and (4) regression of log lean body weight on log body length for individuals. These yield body weight estimates for the Eocene archaeocete Dorudon atrox of 1126, 1118, 1132, and 847 kg, respectively, with consistency and applicability to partial skeletons favoring the first approach. The whole-body weight expected, P_e (in kg), for a given body length, L_i (in cm), is given by log₁₀ P_e?=?2.784 ? log₁₀ L_i???4.429. Negative allometry of body weight and body length (slope 2.784?<?3.000) means that small cetaceans are shorter and more maneuverable than expected for their weight, while large cetaceans are longer and more efficient energetically than expected for their weight. Encephalization is necessarily quantified relative to a reference sample, most mammals are terrestrial, and terrestrial mammals provide a logical baseline. The encephalization residual for living terrestrial mammals as a class (ER_TC), is the difference between observed log₂ brain weight (E_i in g) and expected log₂ brain weight (E_e in g), where the latter is estimated from body weight (P_i in g), as log₂ E_e?=?0.740 ? log₂ P_i???4.004. ER_TC is positive for brains that are larger than expected for a given body size, and negative for brains that are smaller than expected. Base-2 logarithms make the ER_TC scale intuitive, in uniform units of halving or doubling. Encephalization quotients (EQ) are unsuitable for comparison because they are proportions on a non-uniform scale. Middle Eocene archaeocetes have ER_TC values close to ?2 (two halvings compared to expectation), while late Eocene archaeocetes have ER_TC values close to ?1 (one halving compared to expectation). ER_TC is not known for fossil mysticetes, but living mysticetes have ER_TC values averaging about ?2. Oligocene-Recent odontocetes appear to have ER_TC values averaging about +1 (one doubling compared to expectation) through their temporal range. Definitive interpretation of the evolution of encephalization in Cetacea will require better documentation for Oligocene–Recent mysticetes and odontocetes.     

Pattern and process in the geographical ranges of freshwater fishes

North American freshwater fishes were studied to determine whether they displayed the same relationships between log (geographical range size) and log (body size) and the same pattern of range shape as found among North American birds and mammals. The forces that produce these patterns were also investigated. The log (geographical range size) : log (body size) relationship was analysed for 121 North American freshwater fish species. Thirty‐two imperilled species were compared with 89 non‐imperilled species to determine if the overall relationship could result from differential extinction. Range geometries were analysed, within and among habitat guilds, to determine if general patterns could be detected. The log (geographical range size) : log (body size) pattern among freshwater fish species was triangular and qualitatively similar to that found for North American birds and mammals. The results suggest that below a minimum geographical range, the likelihood of extinction increases dramatically for freshwater fishes and that this minimum range size increases with body size. The pattern of fish species’ range shapes differs from that found for other North American vertebrate taxa because, on average, fish possess much smaller ranges than terrestrial species and most fish species’ geographical ranges extend further on a north–south axis than on an east–west axis. The log (geographical range size) : log (body size) pattern reveals that fish species’ geographical ranges are more constrained than those of terrestrial species. The triangular relationship may be caused by differential extinction of species with large bodies and small geographical ranges as well as higher speciation rates of small‐bodied fish. The restricted geographical ranges of freshwater fishes gives them much in common with terrestrial species on oceanic islands. Range shape patterns within habitat guilds reflect guild‐specific historical and current ecological forces. The overall pattern of range shapes emerges from the combination of ecologically different subunits.     

Associations of body mass index and waist:hip ratio with hypertension.

Canada Fitness Survey data for people aged 20 to 69 years were analysed by means of linear discriminant analysis to determine the effect of age, weight relative to height (body mass index) and weight distribution (waist:hip ratio) on hypertension (defined as diastolic blood pressure of 90 mm Hg or more) for both sexes separately. All three variables had independent effects on hypertension, but partial correlation coefficients indicated that the contribution of waist:hip ratio was secondary to that of body mass index. The association of measurements of body fat (five skinfold measurements) with hypertension was also examined; overall these measurements gave no advantage over the more simply measured body mass index. The results confirm the importance of assessing the predominant location of body fat and the body mass index when examining excess weight in relation to disease.     

RELATIONS AMONGST VARIOUS LINEAR MEASUREMENTS AND WEIGHT FOR BLACK RHINOCEROSES IN KENYA

Records of black rhinoceroses obtained from different areas of Kenya suggest a very close relationship between body weight and length and chest girth. The best regressions are: log weight on log length+log girth, and weight on length x girth². The square of the correlation coefficient in both cases is more than 0.98, and the relations appear to be independent of habitat and sex. In contrast the two sexes show marked differences in the relation between front and back horn length with the males tending to grow relatively longer front horns. Attempts to predict the size of the animal and the length of its horns from the spoor were less successful.     

Mammalian reproductive strategies: A generalized relation of litter size to body size

Summary A generalized relationship of litter size to mammalian body size was predicted by a graph model. The model was used to generate hypotheses explaining specific features of variation in gestation time, relative litter weight, birth weight, and reproductive capacity. The predictions were tested by means of data from the literature.Mammals were assumed to maximize neonatal survival of offspring to the limits allowed by litter weight per female body weight. Gestation time correlated negatively with the foetal growth rate of relative litter weight. Gestation time did not correlate with the foetal growth rate of individual offspring.Relative litter weight correlated negatively with adult body weight. This relationship was explained by the higher assimilation rate per unit weight relative to metabolic rate in small mammals.Birth weight correlated positively with body weight. However, small mammals produce larger offspring than predicted by the linear relationship of birth weight to body weight in large mammals. There is obviously a minimum birth weight which cannot be decreased without special arrangements for parental care.The prediction of the relationship of litter size to body size was derived from the relations of relative litter weight and birth weight to body weight. In small mammals (less than 1 kg) litter the correlation was negative. When litter size was compared with body length, the correlation was positive in small mammals (less than 30 cm) and negative in large mammals. In both sets of data there was a negative overall correlation between litter size and body size.Reproductive capacity, defined as the number of offspring per season, correlated negatively with life-span.     

The effect of somatic and gonadal size on the rate of oxygen consumption in the subantarctic echinoid Abatus cordatus (Echinodermata) from Kerguelen

1. The rate of oxygen consumption of this burrowing spatangoid was measured for individuals ranging in size from 3-month old 2.5-mm long juveniles to 39-mm long adults. 2. The decrease in the rate of oxygen consumption/dry weight with increasing body size is greater among mature adults than among juveniles because the increase in aerobic tissue (primarily the test) with body size is less than the increase in anaerobic tissues (mainly the gonads). 3. The rate of oxygen consumption/ash-free dry weight decreased more slowly with increasing body size because of the increase in the level of inorganic material. 4. Replacement of the common fresh weight or dry weight specific oxygen consumption by a more synthetic value calculated from ash-free dry weight specific oxygen consumption measurements, to annulate the body-size effect, is proposed for interspecific comparison over a wide range of body size, taking into account parameters such as temperature.     

Life-history variation within a taxon: a comparative analysis of birds and mammals

Most studies on life-history evolution discuss the necessity of distinguishing between extrinsic and intrinsic sources of variability in life-history traits. I use log/log plots of yearly neonate production in daugters (b) versus adult mortality (Ma) for 75 bird species and 88 mammal species to compare graphically life-history "fields" arranged by these selective forces along a "slow-fast continuum". Under the assumptions of steady-state and linear relationship between adult mortality and reproductive effort, as well as between juvenile survival and relative neonate weight, it is possible to place additional axes in the two-dimentional plot, and to predict covariations among demographic and individual growth traits. The functional regression analysis shows, that the assumptions are completely fulfilled, at least for birds, but mammals show nonlinear relationship between adult mortality and reproductive effort. This can be explained by peculiarities of metabolism and parental care in small mammals with high reproductive output. Hence, for birds the axis of relative neonate weight approximately coincides in direction with the juvenile survivorship axis, but this is not a case for mammals. In both taxa, the relative neonate weight is an invariant in relation to fecundity and adult mortality (but not in relation to adult body weight). This important feature, together with other intrinsic (energetic and phylogenetic) constraints, explains well-documented close covariations among traits, even when the effect of body size is factored out. It is argued that life-history and body size variations in birds and mammals mainly depend on a pattern of temporal resource deficiency, although this impact cannot be separated from that of extrinsic juvenile mortality.     

Estimating consumable biomass from body length and order in insects and spiders

1. Current models used to estimate insect prey biomass for diet studies use whole weight. However, a large proportion of an arthropod's body is taken up by an indigestible exoskeleton, leading to erroneous estimation of the food intake of insectivorous animals. 2. Linear mixed effect models were used to obtain equations to predict consumable biomass from body length for a variety of Neotropical insects and spiders. These data were obtained by feeding taxa of various orders to groups of 100 social spiders and comparing pre‐ and post‐consumption weights using size‐matched controls. 3. Significant linear relationships were found relating body size to consumed biomass for all orders, with slopes ranging from 1.276 to 4.011 and R² values from 0.476 to 0.929. For orders other than spiders and Orthoptera, the increase in weight with size exhibited negative allometric scaling, suggesting a decrease in tissue density, or an increase in internal air space, with size. 4. Although there were significant differences across taxonomic orders in the proportion of biomass consumed, within most orders the proportion consumed did not differ significantly with body size. The estimated regression coefficients may be used by other workers to estimate consumable biomass of arthropod prey for studies requiring large sample sizes or non‐lethal sampling of rare or endangered species.