Intraspecies variation in BMR does not affect estimates of early hominin total daily energy expenditure

We conducted a meta-analysis of 45 studies reporting basal metabolic rate (BMR) data for Homo sapiens and Pan troglodytes to determine the effects of sex, age, and latitude (a proxy for climate, in humans only). BMR was normalized for body size using fat-free mass in humans and body mass in chimpanzees. We found no effect of sex in either species and no age effect in chimpanzees. In humans, juveniles differed significantly from adults (ANCOVA: P < 0.001), and senescent adults differed significantly from adults younger than 50 years (P < 0.001). Europeans differed significantly from tropical populations (P < 0.001). On the basis of these observations, we derived new equations describing the relationship between BMR and body size, and used them to predict total daily energy expenditure (TEE) in four early hominin species. Our predictions concur with previous TEE estimates (i.e. Leonard and Robertson: Am J Phys Anthropol 102 (1997) 265-281), and support the conclusion that TEE increased greatly with H. erectus. Our results show that intraspecific variation in BMR does not affect TEE estimates for interspecific comparisons. Comparisons of more closely related groups such as humans and Neandertals, however, may benefit from consideration of this variation.     

The effect of feeding on CO2 production and energy expenditure in ponies measured by indirect calorimetry and the 13C-bicarbonate technique

Energy expenditure (EE) can be estimated based on respiratory gas exchange measurements, traditionally done in respiration chambers by indirect calorimetry (IC). However, the ¹³C-bicarbonate technique (¹³C-BT) might be an alternative minimal invasive method for estimation of CO₂ production and EE in the field. In this study, four Shetland ponies were used to explore the effect of feeding on CO₂ production and EE measured simultaneously by IC and ¹³C-BT. The ponies were individually housed in respiration chambers and received either a single oral or intravenous (IV) bolus dose of ¹³C-labelled sodium bicarbonate (NaH¹³CO₃). The ponies were fed haylage 3 h before (T₋₃), simultaneously with (T₀) or 3 h after (T₊₃) administration of ¹³C-bicarbonate. The CO₂ produced and O₂ consumed by the ponies were measured for 6 h with both administration routes of ¹³C-bicarbonate at the three different feeding times. Feeding time affected the CO₂ production (P<0.001) and O₂ consumption (P<0.001), but not the respiratory quotient (RQ) measured by IC. The recovery factor (RF) of ¹³C in breath CO₂ was affected by feeding time (P<0.01) and three different RF were used in the calculation of CO₂ production measured by ¹³C-BT. An average RQ was used for the calculations of EE. There was no difference between IC and ¹³C-BT for estimation of CO₂ production. An effect of feeding time (P<0.001) on the estimated EE was found, with higher EE when feed was offered (T₀ and T₊₃) compared with when no feed was available (T₋₃) during measurements. In conclusion, this study showed that feeding time affects the RF and measurements of CO₂ production and EE. This should be considered when the ¹³C-BT is used in the field. IV administration of ¹³C-bicarbonate is recommended in future studies with horses to avoid complex ¹³C enrichment-time curves with maxima and shoulders as observed in several experiments with oral administration of ¹³C-bicarbonate.     

The energetic costs of fighting in the house cricket, Acheta domesticus L

The cost of performing an agonistic behavior, or tactic, willhave consequences for an individual's rate of cost accrual,the tactic's evolutionary stability if used as an assessmentsignal, and its pattern of use in the behavioral choreographyof a contest. Few studies have attempted to quantify the costsof fighting, particularly with regard to energy expenditure.Flow-through respirometry revealed that house cricket malescan expend energy at relatively high rates when fighting (morethan eight times resting levels) depending on the particulartactic performed. Acoustic signalling (stridulation) constitutedthe least costly of seven measured agonistic tactics, whilewrestling with an opponent, the most energetically costly tactic,consumed oxygen at a net rate more than 40 times that of stridulation.Low-cost tactics are used by opponents more frequently thanmore costly tactics, providing evidence for an escalating tacticalconvention based on energetic costs. The moderate energeticcost of some tactics suggests they may function as reliablesignals in the assessment of wrestling ability. Net energy costsper contest increased linearly with contest duration for bothcontest winners and losers, but winners tended to expend moreenergy per contest than losers. The likely fitness effects ofenergy expended while fighting are discussed. The results ofthis study indicate that energy expenditure is an importantcost shaping contest strategies in Acheta domesticus