Relations between abundance, body size and species number in British birds and mammals

1996 ◽  
Vol 351 (1337) ◽  
pp. 265-278 ◽  

British birds and mammals are compared in terms of their frequency distributions of abundance and body mass and in respect of the relation between abundance and body mass. Body masses of non-flying mammals are greater than those of resident birds which are, in turn, heavier than migrants; bats are lightest. The frequency distribution of masses are close to log-Normal for each of these groups, though their variances and skews differ. Differences in mean abundances (which are log-Normally distributed) parallel those in body mass. In each group, abundance declines with body mass: the exponent of the relation is close to the value of —0.75 predicted by the ‘energetic equivalence’ rule though not significantly different from the value of — 1.0 predicted by the ‘biomass equivalence’ rule. At comparable masses, species of non-flying mammals are more abundant than resident birds, migrant birds and bats by approximately 45, 300 and 200 times, respectively. The similarity between birds and bats in this regard may be no more than coincidental but it may be related to ecological similarities related to flight. The metabolic rates of non-flying mammals may be generally lower than those of birds and bats but not sufficiently to account for their much greater abundances.

1969 ◽  
Vol 6 (2) ◽  
pp. 201-211 ◽  
Author(s):  
R. G. McCrossan

Both the oil and gas reserves of Western Canada are log-normally distributed. If the total reserves are separated into groups made up of single types of occurrence, these all display log-normal distributions as well. The parameters of the distributions vary considerably for different groups of genetically related accumulations. Many of the distributions also appear to be heterogeneous, showing distinct bimodality. Several hypotheses can be offered to explain this. For instance, the reserves of the group of smaller sized pools may be under-estimated for lack of sufficient information; secondly, geologically unlike types of pools may be grouped together. If the former is the case, an estimate can be made of the additional oil and gas in aggregate that may be undeveloped in the smaller under-estimated pools. The degree of bimodality may also indicate the maturity of an exploration play. Other possibilities are also considered. The distribution curves for the total reserves show only a generalized picture and obscure the characteristics of the individual distributions of the several types of oil or gas accumulations.


Paleobiology ◽  
2020 ◽  
Vol 46 (3) ◽  
pp. 379-404
Author(s):  
Mateusz Wosik ◽  
Kentaro Chiba ◽  
François Therrien ◽  
David C. Evans

AbstractHadrosaurid dinosaurs, the dominant large-bodied terrestrial herbivores in most Laurasian Late Cretaceous ecosystems, have an exceptional fossil record consisting of many species known from partial ontogenetic series, making them an ideal clade with which to conduct life-history studies. Previous research considered the Dinosaur Park Formation (DPF) of Alberta as an attritional, or time-averaged, sample and interpreted size–frequency distribution of long bones collected from the DPF with three size classes to suggest that hadrosaurids from the DPF attained near-asymptotic body size in under 3 years. This conflicted with previously published osteohistological estimates of 6+ years for penecontemporaneous hadrosaurids from the Two Medicine Formation (TMF) of Montana, suggesting either extreme variation in hadrosaurid growth rates or that size–frequency distributions and/or osteohistology and growth modeling inaccurately estimate ontogenetic age.We tested the validity of the previously proposed size–age relationship of hadrosaurids from the DPF by significantly increasing sample size and combining data from size–frequency distributions and osteohistology across multiple long-bone elements. The newly constructed size–frequency distributions typically reveal four relatively distinct size–frequency peaks that, when integrated with the osteohistological data, aligned with growth marks. The yearling size class was heavily underrepresented in the size–frequency distribution. If not due to preservation, this suggests that either juvenile (<2 years of age) hadrosaurids from the DPF had increased survivorship following an initially high nestling mortality rate or that yearlings were segregated from adults. A growth-curve analysis revealed asymptotic body size was attained in approximately 7 years, which is consistent with hadrosaurids from the TMF. The data suggest size–frequency distributions of attritional samples underestimate age and overestimate growth rates, but when paired with osteohistology can provide unique life-history insights.


2020 ◽  
Vol 126 (6) ◽  
pp. 1017-1027
Author(s):  
Antony van der Ent ◽  
Guillaume Echevarria ◽  
Philip Nti Nkrumah ◽  
Peter D Erskine

Abstract Background and Aims The aim of this study was to test the frequency distributions of foliar elements from a large dataset from Kinabalu Park (Sabah, Malaysia) for departure from unimodality, indicative of a distinct ecophysiological response associated with hyperaccumulation. Methods We collected foliar samples (n = 1533) comprising 90 families, 198 genera and 495 plant species from ultramafic soils, further foliar samples (n = 177) comprising 45 families, 80 genera and 120 species from non-ultramafic soils and corresponding soil samples (n = 393 from ultramafic soils and n = 66 from non-ultramafic soils) from Kinabalu Park (Sabah, Malaysia). The data were geographically (Kinabalu Park) and edaphically (ultramafic soils) constrained. The inclusion of a relatively high proportion (approx. 14 %) of samples from hyperaccumulator species [with foliar concentrations of aluminium and nickel (Ni) &gt;1000 μg g–1, cobalt, copper, chromium and zinc &gt;300 μg g–1 or manganese (Mn) &gt;10 mg g–1] allowed for hypothesis testing. Key Results Frequency distribution graphs for most elements [calcium (Ca), magnesium (Mg) and phosphorus (P)] were unimodal, although some were skewed left (Mg and Mn). The Ni frequency distribution was bimodal and the separation point for the two modes was between 250 and 850 μg g–1. Conclusions Accounting for statistical probability, the established empirical threshold value (&gt;1000 μg g–1) remains appropriate. The two discrete modes for Ni indicate ecophysiologically distinct behaviour in plants growing in similar soils. This response is in contrast to Mn, which forms the tail of a continuous (approximately log-normal) distribution, suggestive of an extension of normal physiological processes.


2019 ◽  
Vol 66 (4) ◽  
pp. 417-424
Author(s):  
Gregorio Moreno-Rueda ◽  
Abelardo Requena-Blanco ◽  
Francisco J Zamora-Camacho ◽  
Mar Comas ◽  
Guillem Pascual

Abstract Predation is one of the main selective forces in nature, frequently selecting potential prey for developing escape strategies. Escape ability is typically influenced by several morphological parameters, such as morphology of the locomotor appendices, muscular capacity, body mass, or fluctuating asymmetry, and may differ between sexes and age classes. In this study, we tested the relationship among these variables and jumping performance in 712 Iberian green frogs Pelophylax perezi from an urban population. The results suggest that the main determinant of jumping capacity was body size (explaining 48% of variance). Larger frogs jumped farther, but jumping performance reached an asymptote for the largest frogs. Once controlled by structural body size, the heaviest frogs jumped shorter distances, suggesting a trade-off between fat storage and jumping performance. Relative hind limb length also determined a small but significant percentage of variance (2.4%) in jumping performance—that is, the longer the hind limbs, the greater the jumping capacity. Juveniles had relatively shorter and less muscular hind limbs than adults (for a given body size), and their jumping performance was poorer. In our study population, the hind limbs of the frogs were very symmetrical, and we found no effect of fluctuating asymmetry on jumping performance. Therefore, our study provides evidence that jumping performance in frogs is not only affected by body size, but also by body mass and hind limb length, and differ between age classes.


2007 ◽  
Vol 7 (4) ◽  
pp. 347-359 ◽  
Author(s):  
Gaurav Ameta ◽  
Joseph K. Davidson ◽  
Jami J. Shah

A new mathematical model for representing the geometric variations of lines is extended to include probabilistic representations of one-dimensional (1D) clearance, which arise from positional variations of the axis of a hole, the size of the hole, and a pin-hole assembly. The model is compatible with the ASME/ ANSI/ISO Standards for geometric tolerances. Central to the new model is a Tolerance-Map (T-Map) (Patent No. 69638242), a hypothetical volume of points that models the 3D variations in location and orientation for a segment of a line (the axis), which can arise from tolerances on size, position, orientation, and form. Here, it is extended to model the increases in yield that occur when maximum material condition (MMC) is specified and when tolerances are assigned statistically rather than on a worst-case basis; the statistical method includes the specification of both size and position tolerances on a feature. The frequency distribution of 1D clearance is decomposed into manufacturing bias, i.e., toward certain regions of a Tolerance-Map, and into a geometric bias that can be computed from the geometry of multidimensional T-Maps. Although the probabilistic representation in this paper is built from geometric bias, and it is presumed that manufacturing bias is uniform, the method is robust enough to include manufacturing bias in the future. Geometric bias alone shows a greater likelihood of small clearances than large clearances between an assembled pin and hole. A comparison is made between the effects of choosing the optional material condition MMC and not choosing it with the tolerances that determine the allowable variations in position.


2007 ◽  
Vol 85 (12) ◽  
pp. 1275-1285 ◽  
Author(s):  
Sebastián P. Luque ◽  
Edward H. Miller ◽  
John P.Y. Arnould ◽  
Magaly Chambellant ◽  
Christophe Guinet

Pre- and post-weaning functional demands on body size and shape of mammals are often in conflict, especially in species where weaning involves a change of habitat. Compared with long lactations, brief lactations are expected to be associated with fast rates of development and attainment of adult traits. We describe allometry and growth for several morphological traits in two closely related fur seal species with large differences in lactation duration at a sympatric site. Longitudinal data were collected from Antarctic ( Arctocephalus gazella (Peters, 1875); 120 d lactation) and subantarctic ( Arctocephalus tropicalis (Gray, 1872); 300 d lactation) fur seals. Body mass was similar in neonates of both species, but A. gazella neonates were longer, less voluminous, and had larger foreflippers. The species were similar in rate of preweaning growth in body mass, but growth rates of linear variables were faster for A. gazella pups. Consequently, neonatal differences in body shape increased over lactation, and A. gazella pups approached adult body shape faster than did A. tropicalis pups. Our results indicate that preweaning growth is associated with significant changes in body shape, involving the acquisition of a longer, more slender body with larger foreflippers in A. gazella. These differences suggest that A. gazella pups are physically more mature at approximately 100 d of age (close to weaning age) than A. tropicalis pups of the same age.


1978 ◽  
Vol 35 (2) ◽  
pp. 184-189 ◽  
Author(s):  
S. J. Westrheim ◽  
W. E. Ricker

Consider two representative samples of fish taken in different years from the same fish population, this being a population in which year-class strength varies. For the "parental" sample the length and age of the fish are determined and are used to construct an "age–length key," the fractions of the fish in each (short) length interval that are of each age. For the "filial" sample only the length is measured, and the parental age–length key is used to compute the corresponding age distribution. Trials show that the age–length key will reproduce the age-frequency distribution of the filial sample without systematic bias only if there is no overlap in length between successive ages. Where there is much overlap, the age–length key will compute from the filial length-frequency distribution approximately the parental age distribution. Additional bias arises if the rate of growth if a year-class is affected by its abundance, or if the survival rate in the population changes. The length of the fish present in any given part of a population's range can vary with environmental factors such as depth of the water; nevertheless, a sample taken in any part of that range can be used to compute age from the length distribution of a sample taken at the same time in any other part of the range, without systematic bias. But this of course is not likely to be true of samples taken from different populations of the species. Key words: age–length key, bias, Pacific ocean perch, Sebastes alutus


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