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.     

Why size matters: altering cell size

Several genes involved in growth control have lately been demonstrated to exhibit more potent effects on cell size than on cell proliferation. Many of these genes direct protein and ribosomal synthesis, highlighting the interdependence between cell size and macromolecular content. The failure to maintain normal cell size when these genes are deregulated suggests that, in certain contexts, cell growth and division are not coupled or coordinated. Several physiological repercussions of altering cell size have been identified.     

Body size of virtual rivals affects ejaculate size in sticklebacks

Sperm competition occurs when sperm of two or more males competeto fertilize a given set of eggs. Theories on sperm competitionexpect males under high risk of sperm competition to increaseejaculate size. Here we confirm this prediction experimentallyin the three-spined stickleback (Gasterosteus aculeatus). Inthis species, sneaking (i.e., stealing of fertilizations byneighboring males) can lead to sperm competition. Sneaking malesinvade foreign nests, and the owners vigorously try to preventthis intrusion. In such fights, male body size is assumed tobe an important predictor of success. Consequently, the riskof sperm competition may depend on the size of a potential competitor.We experimentally confronted males before spawning with eithera large or a small computer-animated rival. We show that malesejaculated significantly more sperm after the presentation ofthe larger virtual rival than after the small stimulus. In addition,the time between the initiation of courting and the spawningwas shorter in the large virtual male treatment. The resultssuggest that stickleback males tailor ejaculate size relativeto the risk of sperm competition perceived by the size of apotential competitor.     

Effective population size of a population with stochastically varying size

For a Wright–Fisher model with mutation whose population size fluctuates stochastically from generation to generation, a heterozygosity effective population size is defined by means of the equilibrium average heterozygosity of the population. It is shown that this effective population size is equal to the harmonic mean of population size if and only if the stochastic changes of population size are uncorrelated. The effective population size is larger (resp. smaller) than the harmonic mean when the stochastic changes of population size are positively (resp. negatively) autocorrelated. These results and those obtained so far for other stochastic models with fluctuating population size suggest that the property that effective population sizes are always larger than the harmonic mean under the fluctuation of population size holds only for continuous time models such as diffusion and coalescent models, whereas effective population sizes can be equal to or smaller than the harmonic mean for discrete time models.     

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.     

Measures of geographic range size: the effects of sample size

A number of methods have been used for quantifying the sizes of the geographic ranges of species. The consequences of different levels of sampling (the proportion of actual spatial occurrences) are explored for eight of these, using data on the occurrences of butterfly species on a 10 × 10 km grid across Britain. For all methods, the percentage error of estimation (PEE) decreases with the number of 10 × 10 km squares which a species occupies, most rapidly for extent measures, and more rapidly for area measures than for measures of numbers of units occupied. The rate of decline in PEE itself falls as sampling effort increases. At a given sampling level, rank correlations between range sizes measured by different methods are generally high, but there is no consistent change in the magnitude of these correlations as the level of sampling increases. The composition of the set of species with the smallest range sizes changes with the level of sampling.     

Effects of temperature and season on egg size, hatchling size and adult size in Notiophilus biguttatus

1. Temperature-induced egg size variation and its effects on successive life stages in the carabid beetle Notiophilus biguttatus were examined.
2. In the laboratory, across temperature regimes, egg size and number were inversely related; number of eggs and total egg mass were higher, but egg size was smaller at high temperatures.
3. Food intake rate was shown not to be involved in the temperature effect on egg size.
4. Within the higher temperature regimes, among females, egg size was negatively correlated with number of eggs and with total egg mass.
5. Data on egg mortality and egg development time did not explain why at low temperature eggs were larger than at high temperature.
6. Larvae hatching from eggs produced at a low temperature were heavier than larvae from eggs produced at a high temperature, irrespective of temperature during development.
7. In a prolonged outdoor experiment (January – July), encompassing the main breeding period of N. biguttatus , egg size decreased and both egg production rate and total egg mass increased in the course of the experiment.
8. In the field, an effect of seasonal change in temperature on adult body size was found; teneral beetles that had their juvenile period early in the season were larger than those that had their juvenile period later in the season.
9. The results of the study suggest a mechanistic explanation in which the egg size response to temperature follows from a difference in temperature sensitivity between two processes in oogenesis; adaptiveness of the temperature response was not clarified.     

Brain size,head size and behaviour of a passerine bird

A recent increase in comparative studies of the ecological and evolutionary consequences of brain size in birds and primates in particular have suggested that cognitive abilities constitute a central link. Surprisingly, there are hardly any intraspecific studies investigating how individuals differing in brain size behave, how such individuals are distributed and how brain size is related to life history and fitness components. Brain mass of the barn swallow Hirundo rustica was strongly predicted by external head volume, explaining 99.5% of the variance, allowing for repeatable estimates of head volume as a reflection of brain size. Repeatability of head volume within and between years was high, suggesting that measurement errors were small. In a 2 years study of 501 individual adult barn swallows, I showed that head volume differed between sexes and age classes, with yearlings having smaller and more variable heads than older individuals, and females having smaller and more variable heads than males. Large head volume was not a consequence of large body size, which was a poor predictor of head volume. Birds with large heads arrived early from spring migration, independent of sex and age, indicating that migratory performance may have an important cognitive component. Head volume significantly predicted capture date and recapture probability, suggesting that head volume is related to learning ability, although morphological traits such as wing length, aspect ratio and wing area were unimportant predictors. Intensity of defence of offspring increased with head volume in females, but not in males. Barn swallows with large heads aggregated in large colonies, suggesting that individuals with large heads were more common in socially complex environments. These results suggest that brain size is currently under natural and sexual selection, and that micro‐evolutionary processes affecting brain size can be studied under field conditions.     

Testis size increases with colony size in cliff swallows

By using a sample of over 800 male cliff swallows (Petrochelidonpyrrhonota) that died during a rare climatic event in our Nebraskastudy area in 1996, we investigated how testis size was relatedto body size, age, parasite load, a bird's past colony-sizehistory, and spleen size. Testis volume increased with bodysize. After correcting for body size, testis volume was lowestfor birds age 1 and 2 years but did not vary with age for males3 years old or more. Birds occupying parasite-free (fumigated)colonies had significantly larger testes than did birds at nonfumigatedsites. Testis volume increased significantly with the size ofthe breeding colonies a bird had used in the past. Testis volumehad no relationship with spleen volume after correcting forbody size. The results show within a species that larger testesare favored in more social environments, probably reflectinga response to increased rates of extrapair copulation (and thussperm competition) among cliff swallows in large colonies. Thepresence of ectoparasites, by inflating levels of plasma corticosterone,may in turn reduce testis mass. These data provide no supportfor the hypothesis that large testes, perhaps by producing moretestosterone, are immunosuppressive and thus costly for thatreason.     

Body size and sexual size dimorphism in calanoid copepods

Patterns of sexual size dimorphism and body size in calanoid copepods are examined. We hypothesize that favorable conditions for development will result in large body size and high sexual size dimorphism among populations of a given species and that differences in this allometric relationship among species is governed by the male's role in insemination. We confirm that there is a greater advantage to large female size, normally the larger sex, when compared to males, hence leading to selection for developmental patterns favoring high size dimorphism. Individuals from populations of four centropagid copepod species were measured; other sizes were obtained from published sources. In the four species we examined, the relationships between prosome length and both clutch size and the ability to produce multiple clutches with one insemination were determined. Results show a trend toward hyperallometry in all centropagid species examined: sexual size dimorphism increases with increasing size. Large females produce larger clutches and more additional clutches on one insemination. That hyperallometry is not observed in diaptomid copepods may result from the greater role the male plays in reproduction. Males are needed for each clutch produced, hence the selective pressure to be larger is greater than that in the centropagidae.     

A matter of size: developmental control of organ size in plants

The intrinsic size of plant organs is determined by developmental signals, yet the molecular and genetic mechanisms that control organ size are largely unknown. Ongoing functional analysis of Arabidopsis genes is defining important regulators involved in these mechanisms. Key features of this control are the coordinated activation of growth and cell division by growth regulators and the maintenance of meristematic competence by the ANT gene, which acts as an organ-size checkpoint. Alterations of genome size by polyploidization and endoreduplication can reset this checkpoint by ploidy-dependent, epigenetically regulated differential gene expression. In addition, the regulation of polarized growth and phytohormone signaling also affect final organ size. These findings reveal unique aspects of plant organ-size control that are distinct from animal organ-size control.     

Spatiotemporal relationship between adult census size and genetic population size across a wide population size gradient

Adult census population size (N) and effective number of breeders (N_b) are highly relevant for designing effective conservation strategies. Both parameters are often challenging to quantify, however, making it of interest to determine whether one parameter can be generalized from the other. Yet, the spatiotemporal relationship between N and N_b has not been well characterized empirically in many taxa. We analysed this relationship for 5–7 consecutive years in twelve brook trout populations varying greatly in N (49‐10032) and N_b (3‐567) and identified major environmental variables affecting the two parameters. N or habitat size alone explained 47–57% of the variance in N_b, and N_b was strongly correlated with effective population size. The ratio N_b/N ranged from 0.01 to 0.45 and increased at small N or following an annual decrease in N, suggesting density‐dependent constraints on N_b. We found no evidence for a consistent, directional difference between variability in N_b and/or N_b/N among small and large populations; however, small populations had more varying temporal variability in N_b/N ratios than large populations. Finally, N_b and N_b/N were 2.5‐ and 2.3‐fold more variable among populations than temporally within populations. Our results demonstrate a clear linkage between demographic and evolutionary parameters, suggesting that N_b could be used to approximate N (or vice versa) in natural populations. Nevertheless, using one variable to infer the other to monitor trends within populations is less recommended, perhaps even less so in small populations given their less predictable N_b vs. N dynamics.     

Genome size of chrysophytes varies with cell size and nutritional mode

The cellular content of nuclear DNA varies up to 200,000-fold between eukaryotes. These differences can arise via different mechanisms. In particular, cell size and nutritional mode may influence evolution of the nuclear DNA content. Chrysophytes comprise organisms with different cell organizations and nutritional modes. Heterotrophic clades evolved independently several times from phototrophic or mixotrophic ancestors. Thus, chrysophytes are an ideal model taxon for investigating the effect of the nutritional mode on cellular DNA content. We investigated the genome size of heterotrophic, mixotrophic, and phototrophic chrysophytes. We demonstrate that cell sizes and genome sizes differ significantly between taxa with different nutritional modes. Phototrophic strains tend to have larger cell volumes and larger genomes than heterotrophic strains do. The investigated mixotrophic strains had intermediate cell volumes and small to intermediate genome sizes. Heterotrophic chrysophytes had the smallest genomes and cell volumes compared to other chrysophytes. In general, genome size increased with cell volume, but cell volume only partially explained the variation in genome size. In particular, genome sizes of mixotrophic strains were smaller than expected based on cell sizes.     

Evolution of litter size

Theories on the evolution of litter size among organisms were reexamined. The competition theories, including that based on the r−K-selection hypothesis, could not explain well why low-fecundity strategies have often evolved in stressful environments such as mountain streams, deep sea and the antarctic, where interspecies competition is considered to be lax. The theory, based on Itô's (1980) concept of the procurability of food by the young, was considered to have greater generality because it could explain not only the above-mentioned cases but also those where small litter size is observed in habitats with high species diversity (where interspecific competition may be keen), such as tropical rain forest. Examination of the process of selection of high-fecundity and low-fecundity genotypes also suggested that the procurability of food by the young can best explain the evolution of low-fecundity. The concept of density-induced dispersal and a distinction between density-dependent and density-independent predation pressures should be incorporated into our discussions on the evolution of reproductive rates.     

Genome size of Streptomyces

Abstract Purified lactate dehydrogenase from Brochothrix thermosphacta is stimulated by Fru-1,6-P₂ and G6P although saturating concentrations are high (> 20 mM). Neither is essential for activity. AMP, ADP and ATP inhibit enzyme activity consistent with either non-competitive (with Fru-1,6-P₂ present) or uncompetitive (G6P present) inhibition. Activity is not dependent on P_i (< 200 mM). Based on ³¹P-NMR of cells, sugar phosphate concentration can reach 30 mM with excess glucose present; NDP and NTP also accumulate to levels that inhibit the isolated enzyme. The effector levels in vitro are therefore appropriate to in vivo metabolism and support a regulatory role for sugar phosphates during pyruvate metabolism in this organism.