Sex-specific survival to maturity and the evolution of environmental sex determination.

Four decades ago, it was proposed that environmental sex determination (ESD) evolves when individual fitness depends on the environment in a sex-specific fashion--a form of condition-dependent sex allocation. Many biological processes have been hypothesized to drive this sex asymmetry, yet a general explanation for the evolution of sex-determining mechanisms remains elusive. Here, we develop a mathematical model for a novel hypothesis of the evolution of ESD, and provide a first empirical test using data across turtles.

Sexual systems and life history of barnacles: a theoretical perspective.

Thoracican barnacles show one of the most diverse sexual systems in animals: hermaphroditism, dioecy (males and females), and androdioecy (males and hermaphrodites). In addition, when present, male barnacles are very small and are called "dwarf males". The diverse sexual systems and male dwarfism in this taxon have attracted both theoretical and empirical biologists.

Inclusive fitness theory and eusociality.

Arising from M. A. Nowak, C.

Reproductive allometry and the size-number trade-off for lizards.

Fundamental to life-history theory is the assumed inverse proportionality between the number of offspring and the resource allocation per offspring. Lizards have been model organisms for empirical tests of this theory for decades; however, the expected negative relationship between clutch size and offspring size is often not detected. Here we use the approach developed by Charnov and Ernest to demonstrate that this often concealed trade-off can be made apparent in an interspecific comparison by correcting for size-dependent resource allocation.

Lifetime reproductive effort.

In a 1966 American Naturalist article, G. C. Williams initiated the study of reproductive effort (RE) with the prediction that longer-lived organisms ought to expend less in reproduction per unit of time.

Maternal condition and facultative sex ratios in populations with overlapping generations.

Facultative investment in offspring sex is related to maternal condition in many organisms. In mammals, empirical support for condition-dependent sex allocation is equivocal, and there is some doubt as to theoretical expectations. Much theory has been developed to make predictions for condition-dependent sex ratios in populations with discrete generations.

Dinosaur fossils predict body temperatures.

Perhaps the greatest mystery surrounding dinosaurs concerns whether they were endotherms, ectotherms, or some unique intermediate form. Here we present a model that yields estimates of dinosaur body temperature based on ontogenetic growth trajectories obtained from fossil bones. The model predicts that dinosaur body temperatures increased with body mass from approximately 25 degrees C at 12 kg to approximately 41 degrees C at 13,000 kg.

The offspring-size/clutch-size trade-off in mammals.

The Smith-Fretwell model for optimal offspring size assumes the existence of an inverse proportional relationship (i.e., trade-off) between the number of offspring and the amount of resources invested in an individual offspring; virtually all of the many models derived from theirs make the same trade-off assumption.

Comment on "The illusion of invariant quantities in life histories".

Nee et al. (Reports, 19 August 2005, p. 1236) used a null model to argue that life history invariants are illusions.

A dimensionless invariant for relative size at sex change in animals: explanation and implications.

Recent comparative studies across sex-changing animals have found that the relative size and age at sex change are strikingly invariant. In particular, 91%-97% of the variation in size at sex change across species can be explained by the simple rule that individuals change sex when they reach 72% of their maximum body size. However, this degree of invariance is surprising and has proved controversial.

Size and temperature in the evolution of fish life histories.

Body size and temperature are the two most important variables affecting nearly all biological rates and times, especially individual growth or production rates. By favoring an optimal maturation age and reproductive allocation, natural selection links individual growth to the mortality schedule. A recent model for evolution of life histories for species with indeterminate growth, which includes most fish, successfully predicts the numeric values of two key dimensionless numbers and the allometry of the average reproductive allocation versus maturation size across species.

Similarity of mammalian body size across the taxonomic hierarchy and across space and time.

Although it is commonly assumed that closely related animals are similar in body size, the degree of similarity has not been examined across the taxonomic hierarchy. Moreover, little is known about the variation or consistency of body size patterns across geographic space or evolutionary time. Here, we draw from a data set of terrestrial, nonvolant mammals to quantify and compare patterns across the body size spectrum, the taxonomic hierarchy, continental space, and evolutionary time.

Effects of body size and temperature on population growth.

For at least 200 years, since the time of Malthus, population growth has been recognized as providing a critical link between the performance of individual organisms and the ecology and evolution of species. We present a theory that shows how the intrinsic rate of exponential population growth, rmax, and the carrying capacity, K, depend on individual metabolic rate and resource supply rate. To do this, we construct equations for the metabolic rates of entire populations by summing over individuals, and then we combine these population-level equations with Malthusian growth.

Effects of size and temperature on developmental time.

Body size and temperature are the two most important variables affecting nearly all biological rates and times. The relationship of size and temperature to development is of particular interest, because during ontogeny size changes and temperature often varies. Here we derive a general model, based on first principles of allometry and biochemical kinetics, that predicts the time of ontogenetic development as a function of body mass and temperature.