Bee foraging ranges and their relationship to body size

Bees are the most important pollinator taxon; therefore, understanding the scale at which they forage has important ecological implications and conservation applications. The foraging ranges for most bee species are unknown. Foraging distance information is critical for understanding the scale at which bee populations respond to the landscape, assessing the role of bee pollinators in affecting plant population structure, planning conservation strategies for plants, and designing bee habitat refugia that maintain pollination function for wild and crop plants. We used data from 96 records of 62 bee species to determine whether body size predicts foraging distance. We regressed maximum and typical foraging distances on body size and found highly significant and explanatory nonlinear relationships. We used a second data set to: (1) compare observed reports of foraging distance to the distances predicted by our regression equations and (2) assess the biases inherent to the different techniques that have been used to assess foraging distance. The equations we present can be used to predict foraging distances for many bee species, based on a simple measurement of body size. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Ornament and body size variation and their measurement in natural populations

Measurement of intrapopulation variation in secondary sexual traits is a priority in the testing of sexual selection models. However, it is important to take care in the choice of materials and delimitation of populations. The use of museum skins to study variation in male tail ornaments may substantially underrepresent the real degree of intrapopulation variation. Data from live animals in specific areas provide more realistic estimates, and should be used whenever possible. I use as an example field data on male ornament length and body size in Vidua macroura (Aves: Ploceidae), a promiscuous, parasitic African finch with elongated tail plumes. Individual males differ in the timing and rate of ornament growth, and females are therefore faced with a large degree of phenotypic variation in male ornament size, even though genetic variation may not be great. By correcting for seasonal variation in the ornament lengths of males caught at different times, I show that mid-season coefficients of variation in ornament length of breeding males in two populations are as high as 18% and 55%. By contrast, tarsus, wing and unornamented tail lengths of the same males vary from 2 to 4%.     

Comparative body size relationships in pocket gophers and their chewing lice

In this paper, we use the method of independent contrasts to study body size relationships between pocket gophers and their chewing lice, a host-parasite system in which both host and parasite phylogcnies are well studied. The evolution of body size of chewing lice appears to be dependent only on the body size of their hosts, which confirms the 1991 findings of Harvey and Keymer. We show that there is a positive relationship between body size and hair-shaft diameter in pocket gophers, and that there is also a positive relationship between body size and head-groove width in chewing lice. Finally, we show a positive relationship between gopher hair-shaft diameter and louse head-groove width. We postulate that changes in body size of chewing lice are driven by a mechanical relationship between the parasite's head-groove dimension and the diameter of the hairs of its host. Louse species livingon larger host species may be larger simply because their hosts have thicker hairs, which requires that the lice have a wider head groove. Our study of gopher hair-shaft diameter and louse head-groove dimensions suggest that there is a 'lock-and-key' relationship between these two anatomical features.     

Longevity is not influenced by prenatal programming of body size

Insulin‐like growth factor (IGF) signaling is essential for achieving optimal body size during fetal development, whereas, in the adult, IGFs are associated with aging and age‐related diseases. However, it is unclear as to what extent lifespan is influenced by events that occur during development. Here, we provide direct evidence that the exceptional longevity of mice with altered IGF signaling is not linked to prenatal programming of body size. Mice null for pregnancy‐associated plasma protein‐A (PAPP‐A), an IGF‐binding protein proteinase that increases local IGF bioavailability, are 60–70% the size of their wild‐type littermates at birth and have extended median and maximum lifespan of 30–40%. In this study, PAPP‐A^?/? mice whose body size was normalized during fetal development through disruption of IgfII imprinting did not lose their longevity advantage. Adult‐specific moderation of IGF signaling through PAPP‐A inhibition may present a unique opportunity to improve lifespan without affecting important aspects of early life physiology.     

Pelvic dimorphism in relation to body size and body size dimorphism in humans

Many mammalian species display sexual dimorphism in the pelvis, where females possess larger dimensions of the obstetric (pelvic) canal than males. This is contrary to the general pattern of body size dimorphism, where males are larger than females. Pelvic dimorphism is often attributed to selection relating to parturition, or as a developmental consequence of secondary sexual differentiation (different allometric growth trajectories of each sex). Among anthropoid primates, species with higher body size dimorphism have higher pelvic dimorphism (in converse directions), which is consistent with an explanation of differential growth trajectories for pelvic dimorphism. This study investigates whether the pattern holds intraspecifically in humans by asking: Do human populations with high body size dimorphism also display high pelvic dimorphism? Previous research demonstrated that in some small-bodied populations, relative pelvic canal size can be larger than in large-bodied populations, while others have suggested that larger-bodied human populations display greater body size dimorphism. Eleven human skeletal samples (total N: male = 229, female = 208) were utilized, representing a range of body sizes and geographical regions. Skeletal measurements of the pelvis and femur were collected and indices of sexual dimorphism for the pelvis and femur were calculated for each sample [ln(M/F)]. Linear regression was used to examine the relationships between indices of pelvic and femoral size dimorphism, and between pelvic dimorphism and female femoral size. Contrary to expectations, the results suggest that pelvic dimorphism in humans is generally not correlated with body size dimorphism or female body size. These results indicate that divergent patterns of dimorphism exist for the pelvis and body size in humans. Implications for the evaluation of the evolution of pelvic dimorphism and rotational childbirth in Homo are considered.     

Testicle size of orang-utans in relation to body size

Few data are available for assessing the relative testicle size of orang-utans, Pongo pygmaeus, so measures were obtained for 31 individuals of varying age. It was shown that the volume of the testicles, calculated from in situ measures of testicle length and breadth, closely approximates testicle weight when multiplied by the specific gravity of solid tissue. Growth curves for body weight and data published for wild specimens were evaluated to obtain the weight most characteristic of male Pongo, and the ratio of testicle weight to body weight was calculated. The mean ratio for individuals with fully adult stature is 0.034, similar to but smaller than that of humans at about 0.050, and larger than the ratios reported for 5 gorillas at 0.013. The testicles mature faster than the body, however, so the mean ratio for young adult orang-utans is about 0.056 and resembles the ratio for humans more closely than the full adults. The differences between the ratios for a monogamous gibbon species, orang-utans, and humans is accounted for when testicle size relative to the weight of the female is considered. This is consistent with a sperm dilution effect produced by variation in the size of the female reproductive tract. The small relative testicle size of the gorilla is anomalous and requires verification as does the application of female size to scale the testicles. © 1993 Wiley-Liss, Inc.     

Do simultaneous hermaphrodites choose their mates? Effects of body size in a planarian flatworm

1. We tested whether or not the simultaneous hermaphrodite Dugesia polychroa mates randomly with respect to partner size, a strong indicator of female fecundity.
2. The number and duration of copulations were recorded in forty-eight pairs over 5 days. To minimize effects of individual differences in copulatory activity, all animals were each tested twice: once with an equally large partner ( n = 24 equal-sized pairs) and once with a partner of different size (smaller or larger, respectively, ratio 1 : 1.5,
n = 24 unequal-sized pairs).
3. The animals copulated frequently. No significant differences were observed between treatments in the number of pairs that copulated. Mating behaviour of equal-sized and unequal-sized pairs was compared in a pair-wise analysis. Latency to the first copulation and the average number of copulations did not differ when mating with an equal- or unequal-sized partner. Average copulation duration increased with increasing size in equal-sized pairs, but not in unequal-sized pairs.
4. In an additional experiment, where three large and three small animals were combined (three replicates) and observed for 1–3 days, the mating pattern did not differ from random mating by size.
5. Our data indicate that in D. polychroa the decision to mate is essentially random with respect to size. We argue that this is not caused by, for example, high costs of mate searching, but that simultaneous hermaphrodites with reciprocal insemination mate indiscriminately when (i) matings are easy to obtain and (ii) the cost of mating is low or compensated for by sperm digestion.     

Optimal body size in bumblebees

Summary It is hypothesized that the body size of a bumblebee will be that size which maximizes its average net rate of energy intake while collecting nectar. A mathematical model is developed with the result that the net rate of energy intake of a nectar-collecting bumblebee is expressed as a function of the body size of the bumblebee. From this model the body size which maximizes the net rate of energy intake (i.e., optimal body size) is found (as the solution of an implicit equation). In this situation the advantage of large size is that larger bumblebees fly faster and hence take less flight time than smaller bumblebees. The disadvantage of larger size is greater energetic costs.The parameters of the model are estimated using data obtained from the foraging behavior of bumblebees on monkshood (Aconitum columbianum). The optimal body size is then calculated for workers of Bombus appositus which obtained almost all their nectar from monkshood. The observed and expected (i.e., optimal) body size are found to be close and not significantly different.The model also predicts that, from the bumblebee's point of view, there should be a positive correlation between the size of the bumblebee and the average amount of nectar obtained per flower. Evidence of this correlation is presented and the possible significance of the correlation from the plant's point of view is discussed. A possible extension of the model to general relationships between predator body size, prey size and prey density is discussed.     

Metabolic rate and body size

In larger animals a considerable part of the total body mass (e.g. body water, dissolved substances, mineral and organic deposits) does not consume significant amounts of oxygen. These materials can be considered to form a metabolically inert infrastructure which mainly serves three functions: (1) structural support to the organism, (2) storage of nutrients (building material and energy stores) and (3) transport and distribution of these materials. Considering the transport and support function of the metabolically inert structures and their interconnections it is likely that the infrastructure will basically show some tree-like, branching building plan. The weight of the metabolically inert infrastructure of an organism, can be given by bW/(c+W), in which W=body weight, b and c are constants. With increasing size the weight of the metabolic inert infrastructure increases disproportionably. Experimental data concerning basic metabolic rate (M) in relation to body weight (W) better fit the equation M=a W(1-bW)/(c+W), (a=constant) than the conventional power law.     

Comparative fecundity, clutch size, ovariole number and egg size of Dacus tryoni and D. jarvisi, and their relationship to body size

Dacus tryoni (Frogg.) (Diptera: Tephritidae) is the main tephritid pest of cultivated fruits in Australia. D. jarvisi (Tryon) is also able to infest these fruits. Some factors influencing the rate at which D. tryoni and D. jarvisi exploit patches of host fruits were examined to determine whether one species may have an advantage when they exploit the same fruits in the field. Measurements of the intrinsic rate of increase, ovariole number, clutch size and egg size and the influence of body size on these parameters were made for both species in the laboratory. Up to 10 weeks of age D. tryoni produced twice as many eggs as D. jarvisi, most during a peak 3–5 weeks after adult emergence. The difference in fecundity up to 10 weeks can be explained partly by the higher number of ovarioles in D. tryoni (38/ovary) compared to D. jarvisi (27/ovary). In addition D. tryoni produces smaller eggs than D. jarvisi and distributes them in smaller clutches; 3–4 eggs/clutch vs 10–15. In both species there was a positive correlation between ovariole number and body size (as measured by wing length). By contrast, egg size remained constant over a broad range of body sizes. The influence of these life history differences on the interaction between D. tryoni and D. jarvisi in the field is discussed.

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Résumé D. tryoni Frogg est la principale téphrididae nuisible aux fruits cultivés en Australie. Cependant, plusieurs autres espèces de Dacus, dont D. jarvisi Tryon sont susceptibles de contaminer ces fruits. Quelques facteurs influant sur le taux de contamination de fruits ont été examinés pour déterminer si une espèce peut être avantagée lors de l'exploitation des mêmes fruits dans la nature. L'influence de la taille de l'adulte sur le taux d'accroissement intrinsèque, sur le nombre d'ovarioles, sur l'effectif des pontes et sur la taille des ufs a été examinée au laboratoire sur les 2 espèces. Pendant les 10 premières semaines, D. tryoni produit 2 fois plus d'ufs que D. jarvisi, la plupart étant pondus entre la 3^e et la 5^e semaines après l'émergence. La production de D. tryoni diminue rapidement après ce maximum. D. jarvisi ne présente pas ce maximum précoce, et la production des ufs se fait au même rythme entre les 3^e et 7^e semaines, avant de diminuer graduellement. La différence de fécondité au bout de 10 semaines peut être expliquée partiellement par le plus grand nombre d'ovarioles de D. tryoni (38/ovaire) contre 24/ovaire pour D. jarvisi. De plus, D. tryoni forme des ufs plus petits que D. jarvisi et l'effectif de chacune de ses pontes est plus limité: 3 à 4 ufs contre 10 à 15. Chez les deux espèces, il y a une relation directe nette entre le nombre d'ovarioles et la taille du corps de la femelle (mesurée par la longueur de l'aile). Par contre, la taille des ufs est indépendante d'une grande gamme de tailles du corps des femelles. Les caractéristiques biologiques de D. tryoni le rendent capable de contaminer rapidement les bouquets de fruits qu'il vient de coloniser, ce qui réduit les disponibilités pour les autres espèces susceptibles de contaminer ces fruits. Dans le cas particulier de D. jarvisi, D. tryoni a peu d'impact sur son niveau de population, puisque D. jarvisi peut exploiter aussi son hôte d'origine, Planchonia careya: Il ne tend à entrer en compétition avec D. tryoni que pour une ou deux générations tardives en été, quand l'hôte partage (la goyave) est souvent abondant. Néanmoins, si les fruits sont rares à cette époque ou si les 2 espèces sont obligées de partager leurs hôtes pendant plusieurs générations (hors de l'aire de Planchonia), D. tryoni aura un avantage certain.

     

Emergent body size of mayfly survivors

1. Employing field-deployed mesocosms, we examined the effects of 12-h pulse and 20-day press (continuous) exposures of the common agricultural insecticide, imidacloprid, on nymph abundance, emergence patterns and adult body size of Epeorus spp. (Heptageniidae) and Baetis spp. (Baetidae).
2. In press exposures, reduced nymph density was driven by reduced survivorship; in pulse exposures, reduced nymph density may reflect increased emergence because of stress.
3. Once exposed to imidacloprid, Epeorus and Baetis mayflies developed less and emerged smaller than their control counterparts. Concentrations as low as 0.1  μ g L⁻¹ (12-h pulse) reduced head length in Baetis and thorax length in Epeorus .
4. In all of the Baetis and Epeorus examined, effects were only found in males. Male survivorship and body size can affect population dynamics. Sublethal doses of this widely applied agricultural insecticide have the potential to reduce reproductive success of mayfly populations.     

Brain size and the diversification of body size in birds

Large brains are associated with increased cognitive skills, enabling animals to use new environments and resources more successfully. Such behavioral flexibility is theoretically expected to have macroevolutionary consequences. First, populations of big-brained individuals should more easily become established in new locations, increasing opportunities for allopatric speciation and decreasing chances that the species as a whole becomes extinct. Second, the ability to use new resources should place new selection pressures on populations, promoting adaptive diversification, a process termed "behavioral drive." In this article, we show that the average brain size of a bird family explains a significant fraction (R2 =0.12, P < .0001 , N= 120 families) of the rate at which body size diversifies within the family. The association is independent of the number of species in the family, geographic range, and correlates of speciosity, providing the first general support for the importance of behavioral drive in evolution.     

Sensitivity of intraspecific latitudinal clines of body size for tetrapods to sampling, latitude and body size

Recent studies have shown that most tetrapod groups (mammals,birds, chelonians, amphibians) show general intraspecific tendenciesfor increasing body size with latitude, whereas squamates (lizardsand snakes) show an intraspecific tendency towards decreasingbody size with latitude. Here I evaluate whether these sizetrends are general by using independent contrasts analysis toinvestigate the dependence of intraspecific size-latitude relationships(r), and the magnitude alone of size-latitude relationships([r]), for tetrapod vertebrates, on sample size, range of latitudessampled, average latitude sampled, and body size. Range of latitudessampled, average latitude sampled, and body size did not influencebody size-latitude relationships (r) or the magnitude aloneof body size-latitude relationship ([r]). Sample size did notinfluence size-latitude relationships (r), but did influencethe magnitude alone of size-latitude relationships ([r]), possiblyindicating increased precision of estimating size-latitude relationshipswith increased sampling. In short, intraspecific size-latituderelationships are similar for species of different sizes, occurringat different latitudes, sampled over different latitudinal ranges,and differing in number of populations sampled (though magnitudealone is influenced by sample size). These results suggest thatintraspecific size-latitude trends are general, and biologicallysignificant (i.e., are not artifacts of sampling), thus deservingexplanation.     

The influence of genetic and environmental factors in estimations of current body size, desired body size, and body dissatisfaction.

The objective was to investigate the genetic epidemiology of figural stimuli. Standard figural stimuli were available from 5,325 complete twin pairs: 1,751 (32.9%) were monozygotic females, 1,068 (20.1%) were dizygotic females, 752 (14.1%) were monozygotic males, 495 (9.3%) were dizygotic males, and 1,259 (23.6%) were dizygotic male-female pairs. Univariate twin analyses were used to examine the influences on the individual variation in current body size and ideal body size. These data were analysed separately for men and women in each of five age groups. A factorial analysis of variance, with polychoric correlations between twin pairs as the dependent variable, and age, sex, zygosity, and the three interaction terms (age x sex, age x zygosity, sex x zygosity) as independent variables, was used to examine trends across the whole data set. Results showed genetic influences had the largest impact on the individual variation in current body size measures, whereas non-shared environmental influences were associated with the majority of individual variation in ideal body size. There was a significant main effect of zygosity (heritability) in predicting polychoric correlations for current body size and body dissatisfaction. There was a significant main effect of gender and zygosity in predicting ideal body size, with a gender x zygosity interaction. In common with BMI, heritability is important in influencing the estimation of current body size. Selection of desired body size for both men and women is more strongly influenced by environmental factors.     

Natural selection on body size is mediated by multiple interacting factors: a comparison of beetle populations varying naturally and experimentally in body size

Body size varies considerably among species and among populations within species, exhibiting many repeatable patterns. However, which sources of selection generate geographic patterns, and which components of fitness mediate evolution of body size, are not well understood. For many animals, resource quality and intraspecific competition may mediate selection on body size producing large-scale geographic patterns. In two sequential experiments, we examine how variation in larval competition and resource quality (seed size) affects the fitness consequences of variation in body size in a scramble-competing seed-feeding beetle, Stator limbatus. Specifically, we compared fitness components among three natural populations of S. limbatus that vary in body size, and then among three lineages of beetles derived from a single base population artificially selected to vary in size, all reared on three sizes of seeds at variable larval density. The effects of larval competition and seed size on larval survival and development time were similar for larger versus smaller beetles. However, larger-bodied beetles suffered a greater reduction in adult body mass with decreasing seed size and increasing larval density; the relative advantage of being large decreased with decreasing seed size and increasing larval density. There were highly significant interactions between the effects of seed size and larval density on body size, and a significant three-way interaction (population-by-density-by-seed size), indicating that environmental effects on the fitness consequences of being large are nonadditive. Our study demonstrates how multiple ecological variables (resource availability and resource competition) interact to affect organismal fitness components, and that such interactions can mediate natural selection on body size. Studying individual factors influencing selection on body size may lead to misleading results given the potential for nonlinear interactions among selective agents.     

Contrasting patterns of body size for Daphnia species that segregate by habitat

Summary We investigate how body size of two coexisting Daphnia species varies among 7 lakes that represent a gradient of predation risk. The two species segregate vertically in stratified lakes; D. galeata mendotae is typically smaller and more eplimnetic than D. pulicaria. The extent of vertical habitat partitioning, however, varies seasonally within and among lakes in apparent response to predation intensity by epilimnetic planktivorous fishes. Daphnia pulicaria uses the epilimnion at low levels of fish predation but is restricted to the hypolimnion under high fish predation, whereas D. galaeta mendotae always utilizes the epilimnion. The species display contrasting patterns of genetic variation in neonate size and size at maturity. D. pulicaria is larger in lakes with higher fish and Chaoborus densities whereas D. galeata mendotae is smaller. This contrast in body size in lakes with high predation is associated with greater habitat segregation in those lakes. In lakes with low predation risk, the two species are similar in body size at birth and maturity.Authorship order alphabetical