Guided by concepts from life history (LH) theory, a large human research literature has tested the hypothesis that exposures to extrinsic mortality (EM) promote the development of faster LH strategies (e.g., earlier/faster reproduction, higher offspring number). A competing model proposes that, because EM in the past was intimately linked to energetic constraints, such exposures specifically led to the development of slower LH strategies. We empirically address this debate by examining (1) LH variation among small-scale societies under different environmental conditions; (2) country-, regional- and community-level correlations between ecological conditions, mortality, maturational timing, and fertility; (3) individual-level correlations between this same set of factors; and (4) natural experiments leveraging the impact of externally-caused changes in mortality on LH traits. Partially supporting each model, we found that harsh conditions encompassing energetic stress and ambient cues to EM (external cues received through sensory systems) have countervailing effects on the development of LH strategies, both delaying pubertal maturation and promoting an accelerated pace of reproduction and higher offspring number. We conclude that, although energetics are fundamental to many developmental processes, providing a first tier of environmental influence, this first tier alone cannot explain these countervailing effects. An important second tier of environmental influence is afforded by ambient cues to EM. We advance a 2-tiered model that delineates this second tier and its central role in regulating development of LH strategies. Consideration of the first and second tier together is necessary to account for the observed countervailing shifts toward both slower and faster LH traits.

The enthalpy of hydration of natural clinoptilolite was determined by isothermal immersion calorimetry on Ca-, Na- and K-exchanged clinoptilolite (Fish Creek Mountains, Nevada). Heats of immersion of clinoptilolite were determined at initial H2O contents ranging from θ = 0.02 to 0.85 (where θ is the ratio [H2O content]/[maximum H2O content]). The heat of immersion (liquid H2O reference state) of Ca-clinoptilolite ranged from -7.5 (θ = 0.87) to -25.7 kJ/mol-H2O (θ = 0.19); values for Na-clinoptilolite ranged from -6.3 (θ = 0.85) to -21.8 kJ/mol-H2O (θ = 0.11); and values for K-clinoptilolite ranged from -7.7 (θ = 0.80) to -24.6 kJ/mol-H2O (θ = 0.02). Linear regression of the calorimetric data provided the following values for the complete heat of immersion (from θ = 0): Ca-clinoptilolite, -30.3 ± 2.0; Na-clinoptilolite, -23.4 ± 0.6; and K-clinoptilolite, -22.4 ± 0.8 kJ/mol-H2O.

The heat of immersion measurements were compared with the enthalpy of hydration results of Carey and Bish (1996) determined in a thermogravimetric study of the same samples. The heat of immersion data are similar but of smaller magnitude than the values of enthalpy of hydration and are believed to be more accurate because they represent direct measurements of this thermodynamic property.

The effect of dehydration of clinoptilolite on the thermal evolution of the potential high-level radioactive waste repository at Yucca Mountain was considered by comparing the amount of energy consumed by clinoptilolite dehydration with the amount of energy necessary to heat rocks lacking hydrous minerals. The extra energy consumed on heating clinoptilolite from 25 to 200 °C ranges between 70 and 80% in excess of that required for nondehydrating materials (that is, clinoptilolite acts as a heat sink). These results indicate that accurate thermohydrologic modeling of rock units at Yucca Mountain should consider the thermal effect of dehydration/hydration processes in clinoptilolite and other hydrous minerals, in addition to the water produced/adsorbed during heating/cooling.

The construction of a free-standing stone wall was a significant occasion in Londinium's history, remarkable for the quantity of masonry used and for the continuing additions to the defences over at least three identifiable phases. Since the local geology in the London Basin does not offer suitable building stone, Londinium's walls offer an exceptional example by which to examine the logistics of construction and the transportation of materials in the context of Romano-British building projects. We examine the sources of the materials used, their transport and the scale of labour and investment involved in the construction of the Landward Wall using an energetics-based methodology. Finally, we provide new insights into Londinium's Landward Wall and the socio-economic and practical implications of its construction. Supplementary material is available online (https://doi.org/10.1017/S0068113X21000088) and comprises technical data related to the architectural energetics.

Both extinct and extant hominin populations display morphological features consistent with Bergmann's and Allen's Rules. However, the functional implications of the morphologies described by these ecological laws are poorly understood. We examined this through the lens of endurance running. Previous research concerning endurance running has focused on locomotor energetic economy. We considered a less-studied dimension of functionality, thermoregulation. The performance of male ultra-marathon runners (n = 88) competing in hot and cold environments was analysed with reference to expected thermoregulatory energy costs and the optimal morphologies predicted by Bergmann's and Allen's Rules. Ecogeographical patterning supporting both principles was observed in thermally challenging environments. Finishers of hot-condition events had significantly longer legs than finishers of cold-condition events. Furthermore, hot-condition finishers had significantly longer legs than those failing to complete hot-condition events. A degree of niche-picking was evident; athletes may have tailored their event entry choices in accordance with their previous race experiences. We propose that the interaction between prolonged physical exertion and hot or cold climates may induce powerful selective pressures driving morphological adaptation. The resulting phenotypes reduce thermoregulatory energetic expenditure, allowing diversion of energy to other functional outcomes such as faster running.

This study examined the effect of including different dietary proportions of starch, protein and lipid, in diets balanced for digestible energy, on the utilisation efficiencies of dietary energy by barramundi (Lates calcarifer). Each diet was fed at one of three ration levels (satiety, 80 % of initial satiety and 60 % of initial satiety) for a 42-d period. Fish performance measures (weight gain, feed intake and feed conversion ratio) were all affected by dietary energy source. The efficiency of energy utilisation was significantly reduced in fish fed the starch diet relative to the other diets, but there were no significant effects between the other macronutrients. This reduction in efficiency of utilisation was derived from a multifactorial change in both protein and lipid utilisation. The rate of protein utilisation deteriorated as the amount of starch included in the diet increased. Lipid utilisation was most dramatically affected by inclusion levels of lipid in the diet, with diets low in lipid producing component lipid utilisation rates well above 1·3, which indicates substantial lipid synthesis from other energy sources. However, the energetic cost of lipid gain was as low as 0·65 kJ per kJ of lipid deposited, indicating that barramundi very efficiently store energy in the form of lipid, particularly from dietary starch energy. This study defines how the utilisation efficiency of dietary digestible energy by barramundi is influenced by the macronutrient source providing that energy, and that the inclusion of starch causes problems with protein utilisation in this species.

Proffitt, Stefanucci, Banton, and Epstein (2003) reported a set of studies showing that the perceived distance to a target is influenced by the effort required to walk to its location. Hutchison and Loomis (H&L) reported an experiment that failed to find a significant influence of effort on indices of apparent distance. There were numerous important differences between the design and methods of H&L's study and those of Proffitt et al. Moreover, there are important theoretical reasons to believe that these differences were responsible for the different results. The theoretical motivation of H&L's studies was also brought into question.

While acknowledging that their design and methods were different from the original Proffitt, Stefanucci, Banton, and Epstein (2003) study, Hutchison and Loomis (H&L) continue to argue that their findings qualify our account of energetic influences on distance perception. This reply provides a brief and focused discussion of the methodological differences between their study and ours and why these differences were likely responsible for the different results. It is also argued that the measures employed by H&L are assessments of apparent location, not apparent distance.

Although the relationship between intestinal parasitism, the ingestion and use of energy, and host survival is expected, little work has been done to outline the effect of such organisms upon their host's nutritional requirements in an ecological context. This study is the first to demonstrate that an intestinal helminth previously reported to be of little or no histopathological consequence, Plagiorhynchus cylindraceus, has a significant detrimental impact upon the flow of food energy through a definitive host, the European starling, Sturnus vulgaris. Within both male and female adult European starlings reductions in standard metabolic rates occurred as the result of initial infection, indicating that the host's basal metabolism/thermal regulatory abilities were altered. Moreover, initially infected male starlings, but not females, had an increased consumption and excretion of energy and maintained lower average daily body weights versus controls when temperature stressed. These results appear to be due to either a parasite-mediated alteration in host activity and/or to the disruption of host-digestive abilities. Additionally, these data indicate that, overall, male and female S. vulgaris respond differently to infection and that intestinal helminths normally thought to be of little or no pathological consequence to the host are factors that should be addressed in future studies regarding animal energetics, ecology, and behaviour.

Human susceptibility to obesity is an unusual phenomenon amongst animals. An evolutionary analysis, identifying factors favouring the capacity for fat deposition, may aid in the development of preventive public health strategies. This article considers the proximate causes, ontogeny, fitness value and evolutionary history of human fat deposition. Proximate causes include diet composition, physical activity level, feeding behaviour, endocrine and genetic factors, psychological traits, and exposure to broader environmental factors. Fat deposition peaks during late gestation and early infancy, and again during adolescence in females. As in other species, human fat stores not only buffer malnutrition, but also regulate reproduction and immune function, and are subject to sexual selection. Nevertheless, our characteristic ontogenetic pattern of fat deposition, along with relatively high fatness in adulthood, contrasts with the phenotype of other mammals occupying the tropical savannah environment in which hominids evolved. The increased value of energy stores in our species can be attributed to factors increasing either uncertainty in energy availability, or vulnerability to that uncertainty. Early hominid evolution was characterised by adaptation to a more seasonal environment, when selection would have favoured general thriftiness. The evolution of the large expensive brain in the genus Homo then favoured increased energy stores in the reproducing female, and in the offspring in early life. More recently, the introduction of agriculture has had three significant effects: exposure to regular famine; adaptation to a variety of local niches favouring population-specific adaptations; and the development of social hierarchies which predispose to differential exposure to environmental pressures. Thus, humans have persistently encountered greater energy stress than that experienced by their closest living relatives during recent evolution. The capacity to accumulate fat has therefore been a major adaptive feature of our species, but is now increasingly maladaptive in the modern environment where fluctuations in energy supply have been minimised, and productivity is dependent on mechanisation rather than physical effort. Alterations to the obesogenic environment are predicted to play a key role in reducing the prevalence of obesity.

A female Antarctic krill loses 34% of its body mass when it lays a batch of eggs. This represents a considerable input of energy which was estimated using a combination of measured mass and energy differences in female krill and from the measured energetic content of ovarian tissue. Large (c. 50 mm) female krill lose 2.9–3.8 kJ each time a batch of eggs is laid. Calculations using this figure indicate that multiple spawning by Antarctic krill in a season would require above average phytoplankton concentrations (> 0.5 μg chl a 1−1) and filtration rates which are close to the maximum reported (> 10 l h−1).

Many small carnivores include rodents in their diet. However, due to varying evolutionary strategies, carnivores differ in their metabolism and energy requirements. Hence, comparisons of diet between carnivores would be more meaningful if the body size and energetics of the predators are considered. The diet of three small carnivores (jungle cat Felis chaus; caracal Caracal caracal; golden jackal Canis aureus) from a semi-arid part of western India was studied through scat analysis, and the importance of rodents in their diet was estimated as a percentage of their daily energy requirement. Although percentage frequency in scats and biomass consumption showed rodents to be equally important to all three carnivores, energy calculations showed that rodents were more important as prey for the felids than the jackal. Up to 70% of the daily metabolizable energy in felids was obtained from rodents, as compared to 45% in the jackal. Rodents are generally viewed as pests, and their importance to the small carnivore community is overlooked. Change in land use over the decades in the arid/semi-arid tract of western India has led to several adverse as well as favourable modifications in rodent assemblages, which could influence the persistence of species like the caracal and jungle cat in this region, that largely depend on rodents for their survival.

During terrestrial locomotion, frogs use two distinct gaits: out-of-phase leg movements associated with slow crawling behaviour and in-phase leg movements during fast jumps. In Rana esculenta, crawling occurs during feeding, while jumping is used as an escape strategy. We examined whether a similar velocity-dependent gait shift appears in swimming R. esculenta. Typically, swimming frogs propel themselves by kicking both hind limbs simultaneously. Observations of out-of-phase leg movements in swimming frogs have been reported, but were usually assumed to be associated only with directional changes. We demonstrate that alternating-leg swimming is used quite frequently and that it results in a significantly lower velocity to the one obtained by using in-phase leg movements. This difference is likely to be associated with energetic costs. Mathematical estimates of positive mechanical work required to move the centre of mass revealed that out-of-phase swimming is energetically less expensive than the in-phase gait at a comparable speed, but may not be efficient at high speeds. Possible explanations for this phenomenon are higher inertial energy losses for in-phase swimming, but at high speeds jet propulsion and an interaction effect may gain importance.

North Atlantic harbour porpoises Phocoena phocoena (L.) face considerable energetic challenges, as they are relatively small marine mammals with an intense reproductive schedule and a cold-water habitat. Post-natal growth of these porpoises was described using ontogenetic allometry and body composition techniques. The cross-sectional sample contained robust calves, immature, and mature porpoises (n = 122) incidentally killed in commercial fishing operations between 1992 and 1998. Total mass and the mass of 26 body components were measured using a standard dissection protocol. Most body components grew similarly in female and male porpoises. Blubber, brain and skull were negatively allometric, while muscle and reproductive tissues exhibited positive allometry. Female heart, liver, intestine and mesenteric lymph node grew at significantly higher rates than in males. Male locomotor muscle and pelvic bones grew significantly faster than in females. High growth rates for visceral and reproductive organs in porpoises, relative to other mammals, may underlie their early maturation and support their intensive, annual reproductive schedule. Relative to other cetaceans, porpoises seem to allocate a larger percentage of their total body mass to blubber. This allocation to blubber, which is greatest in calves (37% of body mass), may provide harbour porpoises with the thermal insulation required to live in cold water. The factors influencing growth rates and differential investments in body composition seem to change at various stages of a porpoise's life. Energy allocation in porpoises seems to shift from an emphasis on developing an insulative blubber layer in young animals to preparing the body for annual reproduction at sexual maturity.

This review summarizes information on filial cannibalism (the act of eating one's own offspring) in teleost fish. Cannibalistic parents can either consume their whole brood (total filial cannibalism), or eat only some of the eggs in the nest (partial filial cannibalism). Offspring consumption has been argued to be adaptive under the assumption that offspring survival is traded against feeding, and that offspring can act as an alternative food source for the parents. The evidence supporting the basic predictions formulated under these assumptions is summarized for both total and partial filial cannibalism. These two forms of cannibalism differ significantly since the former represents an investment only in future reproductive success, whereas the latter can affect both present and future reproductive success. Despite a few inconsistencies in the data from laboratory and field studies, the energy-based explanation appears valid for both forms of cannibalism. Alternative non-energy-based explanations are considered, but they are unable to account for the wide distribution of this behaviour in teleosts. The intersexual conflict arising from attempts of the non-cannibal sex to minimize the cost of filial cannibalism is also discussed, together with the potential effect of this behaviour on the operational sex ratio at a population level.

The energetics and burrowing behaviour of the semifossorial Octodon degus (Rodentia: Octodontidae) were investigated and compared with that of more specialized fossorial rodents. An open-flow respirometry system was used to record energy expenditure of single degus inside respirometers partially filled with soft (moist) or hard (dry) soil. In addition, digging behaviour was recorded in groups of three animals inside a large terrarium under controlled conditions of food, photoperiod and temperature. In the field, the digging activity of degus was monitored, along with seasonal variations in rainfall, content of soil moisture and soil hardness. Mass-specific metabolic rate during digging was found to be higher in animals burrowing in soft soils compared to hard soil. However, animals burrowing in soft soil removed more soil per min than animals in hard soil. Thus, gram per gram, excavating in hard soil was energetically more expensive. The digging cost of semifossorial degus tends to be either similar to or above those of similarly sized, but more fossorial, rodents. In the field, heightened digging activity coincided with the occurrence of rainfall, greater content of soil moisture and relatively soft soil conditions. Degus generally use their front feet and teeth to shear the soil; disposal of accumulated debris being carried out by moving their front and hind feet backwards. We also observed the establishment of digging chains when two or three individuals burrowed at the same site. As far as digging is concerned, the behaviour of degus is similar to that of other fossorial rodents, such as African bathyergids and the more closely related South American ctenomyids.