Energy intake and utilisation by nursing bearded seal (Erignathus barbatus) pups from Svalbard,Norway

In this study we measure energy intake via milk in nursing bearded seal (Erignathus barbatus) pups and determine how this energy is allocated into metabolism and storage of new tissues. This was accomplished using longitudinal mass gain records and the doubly labelled water technique on nursing pups in combination with cross-sectional data on changes in milk composition from bearded seal mothers. The pups (n=3) were all less than a week old at the start of the experiments. Pups gained 3.3±0.4 kg·day^-1 of which 50% was fat, 14% protein and 36% water. Average daily water influx for the pups was 69.5±9.0 ml · kg^-1· day^-1. Average CO₂ production during the study period was 0.99±0.10 ml·g^-1·h^-1, which corresponds to a field metabolic rate of 642±67 kJ·kg^-1· day^-1, or 6.0±0.5 times the predicted basal metabolic rate according to Kleiber (1975). The pups drank an average of 7.6±0.5 kg of milk daily. This corresponds to a daily energy intake of 154±8 MJ, 47±14% of which was stored as new body tissue. Despite this high energy intake bearded seal pups do not get as fat as do other nursing phocids. This is in part due to their larger body size but also due to their very active aquatic lifestyle and the lower and more consistent fat content of the milk compared to other phocid species. Bearded seal mothers forage during lactation and may also be involved in teaching their pups to feed independently. All these data suggest that the lactation strategy of bearded seals differs from the phocid norm.     

Integrated control of potato cyst nematodes using small amounts of nematicide and potatoes with partial resistance

The control of potato cyst nematode (PCN) by less than approved amounts of nematicide combined with partially resistant potato clones was studied in a series of field experiments. On a site heavily infested with Globodera pallida only the most resistant clone (12380ac2) decreased the population density in untreated soil. With aldicarb at its full approved rate (3·36 kg ha^-1) numbers of PCN were decreased under all the genotypes, including the non-resistant Maris Piper. Aldicarb at 1·68 kg ha^-1significantly decreased populations on all clones except 12380ac2. Aldicarb at 0·84 kg ha^-1still significantly decreased population densities and multiplication rates of G. pallida on two clones with intermediate resistance (12243acl and 11233ab22). At two G. rostochiensis sites with light infestations nematode multiplication rates were greater and the control given by aldicarb and partially resistant genotypes of potato was not as great as that at the site with G. pallida. Tuber yields were not increased by the application of aldicarb at the G. rostochiensis infested sites. However, at the site heavily infested with G. pallida the yield of the most intolerant genotype (12380ac2) was increased seven-fold by the full rate of aldicarb (3·36 kg ha^-1) and four-fold by the quarter rate (0·84 kg ha^-1)-Yield of the most tolerant genotype (12243acl) was unaffected by the application of aldicarb.     

Comparative analysis of the digestive efficiency and nitrogen and energy requirements of the phyllostomid fruit-bat (Artibeus jamaicensis) and the pteropodid fruit-bat (Rousettus aegyptiacus)

Nitrogen (N) and energy (E) requirements of the phyllostomid fruit bat, Artibeus jamaicensis, and the pteropodid fruit bat Rousettus aegyptiacus, were measured in adults that were fed on four experimental diets. Mean daily food intake by A. jamaicensis and R. aegyptiacus ranged from 1.1–1.6 times body mass and 0.8–1.0 times body mass, respectively. Dry matter digestibility and metabolizable E coefficient were high (81.1% and 82.4%, respectively) for A. jamaicensis and (77.5% and 78.0%, respectively) for R. aegyptiacus. Across the four diets, bats maintained constant body mass with mean metabolizable E intakes ranging from 1357.3 kJ · kg^−0.75 · day⁻¹ to 1767.3 kJ · kg^−0.75 · day⁻¹ for A. jamaicensis and 1282.6–1545.2 kJ · kg^−0.75 · day⁻¹ for R. aegyptiacus. Maintenance E costs were high, in the order of 3.6–5.4 times the basal metabolic rate (BMR). It is unlikely that the E intakes that we observed represent a true measure of maintenance E requirements. All evidence seems to indicate that fruit bats are E maximizers, ingesting more E than required and regulating storage by adjusting metabolic output. We suggest that true maintenance E requirements are substantially lower than what we observed. If it follows the eutherian norm of two times the BMR, fruit bats must necessarily over-ingest E on low-N fruit diet. Dietary E content did affect N metabolism of A. jamaicensis. On respective low- and high-E diets, metabolic fecal N were 0.492 mg N · g⁻¹ and 0.756 mg N · g⁻¹ dry matter intake and endogenous urinary N losses were 163.31 mg N · kg^−0.75 · day⁻¹ and 71.54 mg N · kg^−0.75 · day⁻¹. A. jamaicensis required 332.3 mg · kg^−0.75 · day⁻¹ and 885.3 mg · kg^−0.75 · day⁻¹ of total N on high- and low-E diets, respectively, and 213.7 mg · kg^−0.75 · day⁻¹ of truly digestible N to achieve N balance. True N digestibilities were low (29% and 49%) for low- and high-E diets, respectively. For R. aegyptiacus, metabolic fecal N and endogenous urinary N losses were 1.27 mg N · g⁻¹ dry matter intake and 96.0 mg N · kg^−0.75 · day⁻¹, respectively, and bats required 529.8 mg · kg^−0.75 · day⁻¹ (total N) or 284.0 mg · kg^−0.75 · day⁻¹ (truly digestible N). True N digestibility was relatively low (50%). Based on direct comparison, we found no evidence that R. aegyptiacus exhibits a greater degree of specialization in digestive function and N retention than A. jamaicensis. When combined with results from previous studies, our results indicate that all fruit bats appear to be specialized in their ability to retain N when faced with low N diet. Accepted: 24 November 1998     

Estimated Impact of feral house mice on sub-Antarctic invertebrates at Marion Island

Summary The energy metabolism of feral house mice Mus musculus was established on sub-Antarctic Marion Island, using the doubly-labelled water turnover technique. Mean water influx was 565 ml kg^-1 day^-1 and mean CO₂ production was 5.41 ml g^-1 h^-1, i.e. 3375 kJ kg^-1 day^-1. From the energy content of the main items (Lepidoptera larvae, Curculionidae) in the diet of the mice it was estimated that the dry mass of food consumed was 3.5 g mouse^-1 day^-1. The overall impact of mice on invertebrates, based on mean mouse density and the mean percentage invertebrates in the diet, was estimated at 108 g ha^-1 day^-1 or 39.4 kg ha^-1 y^-1 (dry mass). Greatest predation pressure was on larvae of the flightless moth Pringleophaga marioni: 65 g ha^-1 day^-1 or 23.7 kg ha^-1 y^-1. Insect biomass is lower on Marion Island than on nearby Prince Edward Island, which is mouse-free. It is suggested that populations of certain insects on Marion Island are depressed by the alien mice.     

Aerobic scope for activity in age 0 year Atlantic cod Gadus morhua

Key components of swimming metabolism: standard metabolism (R_s), active metabolism (R_a) and absolute aerobic scope for activity (R_a–R_s) were determined for small age 0 year Atlantic cod Gadus morhua. Gadus morhua juveniles grew from 0·50 to 2·89 g wet body mass (M_WB) over the experimental period of 100 days, and growth rates (G) ranged from 1·4 to 2·9% day^?1, which decreased with increasing size. Metabolic rates were recorded by measuring changes in oxygen consumption over time at different activity levels using modified Brett‐type respirometers designed to accommodate the small size and short swimming endurance of small fishes. Power performance relationships were established between oxygen consumption and swimming speed measurements were repeated for individual fish as each fish grew. Mass‐specific standard metabolic rates () were calculated from the power performance relationships by extrapolating to zero swimming speed and decreased from 7·00 to 5·77 μmol O₂ g^?1 h^?1, mass‐specific active metabolic rates () were calculated from extrapolation to maximum swimming speed (U_max) and decreased from 26·18 to 14·35 μmol O₂ g^?1 h^?1 and mass‐specific absolute scope for activity was calculated as the difference between active and standard metabolism () and decreased from 26·18 to 14·35 μmol O₂ g^?1 h^?1 as M_WB increased. Small fish with low R_s had bigger aerobic scopes but, as expected, R_s was higher in smaller fish than larger fish. The measurements and results from this study are unique as R_s, R_a and absolute aerobic scopes have not been previously determined for small age 0 year G. morhua.     

Movement patterns of catfishes (Ariidae) in a tropical semi‐arid estuary

From December 2005 to November 2006, 216 samples were taken from the main channel of the Goiana Estuary, representing a total sampled area of 23 ha. Ariidae species were the most abundant in density (1600 individuals ha^?1, 53%) and biomass (18 813 g ha^?1, 63%). Cathorops spixii was the most abundant in density (1340 individuals ha^?1) and biomass (14 203 g ha^?1). The variables: number of species, total density and biomass, showed significant interactions between the factors of areas and seasons (P < 0·01). The highest total density (7394 individuals ha^?1) and biomass (70 292 g ha^?1) occurred in the middle and upper estuaries, respectively, during the early‐rainy season. The density of C. spixii differed significantly between areas and seasons (P < 0·01), while Cathorops agassizii differed significantly only between seasons (P < 0·01). The biomass differed significantly for the species C. spixii, C. agassizii and Sciades herzbergii between seasons, and C. spixii and C. agassizii between areas. Also, the density and biomass of C. spixii and C. agassizii showed interaction between areas and seasons. Only the biomass of S. herzbergii showed interaction between areas and seasons (P < 0·01). This indicates that seasonal variations influenced the distribution of Ariidae species in the different areas of the Goiana Estuary. Moreover, canonical correspondence analysis highlighted a strongly significant correlation (P < 0·01) between the seasonal variations of the environmental gradients (salinity and water temperature) and distribution of catfishes. The management and conservation of estuaries should take into account the life cycle of these species in different estuarine areas and hydrological seasons.     

Energy and substrate metabolism during a 42-day bed-rest in a head-down tilt position in humans

Microgravity-induced changes in body composition (decrease in muscle mass and increase in fat mass) and energy metabolism were studied in seven healthy male subjects during a 42-day bed-rest in a head-down tilt (HDT) position. Resting energy expenditure (REE), fat and glucose oxidation were estimated by indirect calorimetry on days 0, +8 and +40 of the HDT period. Assessments were performed both in post-absorptive conditions and following two identical test meals given at 3-h intervals. Body composition (dual x-ray absorptiometry) was measured on days 0, +27, +42. Mean post-absorptive lipid oxidation decreased from 53 (SEM 8) mg · min⁻¹ (day 0) to 32 (SEM 10) mg · min⁻¹ (day 8, P=0.04) and 36 (SEM 8) mg · min⁻¹ (day 40, P=0.06). Mean post-absorptive glucose oxidation rose from 126 (SEM 15) mg · min⁻¹ (day 0) to 164 (SEM 14) mg · min⁻¹ (day 8, P=0.04) and 160 (SEM 20) mg · min⁻¹ (day 40, P=0.07). Mean fat-free mass (FFM) decreased between days 0 and 42 [58.0 (SEM 1.8) kg and 55.3 (SEM 1.7) kg, P<0.01] while fat mass increased without reaching statistical significance. The mean REE decreased from 1688 (SEM 50) kcal · day⁻¹ to 1589 (SEM 42) kcal · day⁻¹ (P=0.056). Changes in REE were accounted for by changes in FFM. Mean energy intake decreased from 2532 (SEM 43) kcal · day⁻¹ to 2237 (SEM 50) kcal · day⁻¹ (day 40, P<0.01) with only a minor decrease in the proportion of fat. We concluded that changes in fat oxidation at the whole body level can be found during HDT experiments. These changes were related to the decrease in FFM and could have promoted positive fat balance hence an increase in fat mass. Accepted: 26 March 1998     

Glucose uptake rate as a tool to estimate hybridoma growth in a packed bed bioreactor

The immobilisation of cells in a perfusion culture allows to obtain a high cell concentration and an efficient removal of the catabolites without cell loss. A disadvantage of this system is that the cell density cannot be directly monitored. The cellular metabolism is just followed by online measurements of pH and dissolved oxygen (DO) and off-line determinations of residual metabolites. In this article, we report a high cell density achieved by the cultivation of a hybridoma in a bubble-column bioreactor filled with hollow glass cylinders. The parameters monitored during the cultivation were pH, temperature, DO, glucose, lactate and monoclonal antibody. The glucose uptake rate was used to estimate the cell concentration along the time. The maximum cell concentration calculated for the considered cultivation time was 2.7?×?10⁷ cell?·?ml^?1. The glucose concentration in the media decreased stepwise twice, causing a decrease on the specific growth rate, while maintaining high antibody productivity levels. Maximum monoclonal antibody productivity was 503?μg?·?l^?1?·?day^?1 and specific productivity, considering calculated cell density, was 0.019?ng?·?cell^?1?·?day^?1.     

Water and sodium balances and metabolic physiology of house mice (Mus domesticus) and short-tailed mice (Leggadina lakedownensis) under laboratory conditions

A laboratory study investigated the metabolic physiology, and response to variable periods of water and sodium supply, of two arid-zone rodents, the house mouse (Mus domesticus) and the Lakeland Downs short-tailed mouse (Leggadina lakedownensis) under controlled conditions. Fractional water fluxes for M. domesticus (24 ± 0.8%) were significantly higher than those of L. lakedownensis (17 ± 0.7%) when provided with food ad libitum. In addition, the amount of water produced by M. domesticus and by L. lakedownensis from metabolic processes (1.3 ± 0.4 ml · day⁻¹ and 1.2 ± 0.4 ml · day⁻¹, respectively) was insufficient to provide them with their minimum water requirement (1.4 ± 0.2 ml · day⁻¹ and 2.0 ± 0.3 ml · day⁻¹, respectively). For both species of rodent, evaporative water loss was lowest at 25 °C, but remained significantly higher in M. domesticus (1.1 ± 0.1 mg H₂O · g^−0.122 · h⁻¹) than in L. lakedownensis (0.6 ± 0.1 mg H₂O · g^−0.122 · h⁻¹). When deprived of drinking water, mice of both species initially lost body mass, but regained it within 18 days following an increase in the amount of seed consumed. Both species were capable of drinking water of variable saline concentrations up to 1 mol · l⁻¹, and compensated for the increased sodium in the water by excreting more urine to remove the sodium. Basal metabolic rate was significantly higher in M. domesticus (3.3 ± 0.2 mg O₂ · g^−0.75 · h⁻¹) than in L. lakedownensis (2.5 ± 0.1 mg O₂ · g^−0.75 · h⁻¹). The study provides good evidence that water flux differences between M. domesticus and L. lakedownensis in the field are due to a requirement for more water in M. domesticus to meet their physiological and metabolic demands. Sodium fluxes were lower than those observed in free-ranging mice, whose relatively high sodium fluxes may reflect sodium associated with available food. Accepted: 16 August 1999     

Energetics during nursing and early postweaning fasting in hooded seal (Cystophora cristata ) pups from the Gulf of St Lawrence, Canada

In this study we measured growth and milk intake and calculated energy intake and its allocation into metabolism and stored tissue for hooded seal (Cystophora cristata) pups. In addition, we measured mass loss, change in body composition and metabolic rate during the first days of the postweaning fast. The mean body mass of the hooded seal pups (n = 5) at the start of the experiments, when they were new-born, was 24.3 ± 1.3 kg (SD). They gained an average of 5.9 ± 1.1. kg · day⁻¹ of which 19% was water, 76% fat and 5% protein. This corresponds to an average daily energy deposition of 179.8 ± 16.0 MJ. The pups were weaned at an average body mass of 42.5 ± 1.0 kg 3.1 days after the experiment was initiated. During the first days of the postweaning fast the pups lost an average of 1.3 ± 0.5␣kg of body mass daily, of which 56% was water, 16% fat and 28% protein. During the nursing period the average daily water influx for the pups was 124.6 ± 25.8 ml · kg⁻¹. The average CO₂ production during this period was 1.10 ± 0.20 ml · g⁻¹ · h⁻¹, which corresponds to a field metabolic rate of 714 ± 130 kJ ·  kg⁻¹ · day⁻¹, or 5.8 ± 1.1 times the predicted basal metabolic rate according to Kleiber (1975). During the postweaning fast the average daily water influx was reduced to 16.1 ± 6.6 ml · kg⁻¹. The average CO₂ production in␣this period was 0.58 ± 0.17 ml · g⁻¹ · h⁻¹ which corresponds to a field metabolic rate of 375 ± 108 kJ · kg⁻¹ · day⁻¹ or 3.2 ± 0.9 times the predicted basal metabolic rate. Average values for milk composition were 33.5% water, 58.6% fat and 6.2% protein. The pups drank an average of 10.4 ± 1.8␣kg of milk daily, which represents an energy intake of 248.9 ± 39.1 MJ · day⁻¹. The pups were able to store 73.2 ± 7.7% of this energy as body tissue. Accepted: 15 August 1996     

Field metabolic rates and water influxes of two sympatric Gerbillidae:Gerbillus allenbyi andG. pyramidum

Summary Two primarily granivorous rodents of Old World deserts,Gerbillus allenbyi (mean adult body mass=26 g) andG. pyramidum (mean adult body mass=40 g), coexist in sandy habitats in the northwestern Negev desert. Both species are burrow dwellers and are nocturnal; however, in their overall distributions,G. pyramidum occurs in more extreme deserts than doesG. allenbyi. In comparing field metabolic rate (FMR) and water influx of the twoGerbillus species, we considered two alternative hypotheses: (1) given the difference in their overall distributions,G. pyramidum has a lower FMR and water influx thanG. allenbyi, and (2) given the similarity in their diets, and that we worked with sympatric populations, FMR and water influx are similar. The latter alternative proved to be correct. Field metabolic rates in summer were 7.29 kJ · g^-0.51 · day^-1 forG. allenbyi and 7.74 kJ · g^-0.51 · day^-1 forG. pyramidum, values that were 69.3% and 74.5%, respectively, of those predicted for rodents of their body masses. Summer water influx ofG. allenbyi was 0.167 ml · g^-0.90 · day^-1 and that ofG. pyramidum was 0.144 ml · g^-0.90 · day^-1; these values were 79.4% and 68.6%, respectively, of water influxes predicted for rodents of their body masses. When compared allometrically, there were no interspecific differences in any of the measurements.     

Methanogenesis,sulfate reduction and crude oil biodegradation in hot Alaskan oilfields

Petrochemical and geological evidence suggest that petroleum in most reservoirs is anaerobically biodegraded to some extent. However, the conditions for this metabolism and the cultivation of the requisite microorganisms are rarely established. Here, we report on microbial hydrocarbon metabolism in two distinct oilfields on the North Slope of Alaska (designated Fields A and B). Signature anaerobic hydrocarbon metabolites were detected in produced water from the two oilfields offering evidence of in situ biodegradation activity. Rate measurements revealed that sulfate reduction was an important electron accepting process in Field A (6–807 µmol S l^?1 day^?1), but of lesser consequence in Field B (0.1–10 µmol S l^?1 day^?1). Correspondingly, enrichments established at 55°C with a variety of hydrocarbon mixtures showed relatively high sulfate consumption but low methane production in Field A incubations, whereas the opposite was true of the Field B enrichments. Repeated transfer of a Field B enrichment showed ongoing methane production in the presence of crude oil that correlated with ≥ 50% depletion of several component hydrocarbons. Molecular‐based microbial community analysis of the methanogenic oil‐utilizing consortium revealed five bacterial taxa affiliating with the orders Thermotogales, Synergistales, Deferribacterales (two taxa) and Thermoanaerobacterales that have known fermentative or syntrophic capability and one methanogen that is most closely affiliated with uncultured clones in the H₂‐using family Methanobacteriaceae. The findings demonstrate that oilfield‐associated microbial assemblages can metabolize crude oil under the thermophilic and anaerobic conditions prevalent in many petroleum reservoirs.     

An energy budget for juvenile thick-lipped mullet, Crenimugil labrosus (Risso)

A series of experiments were carried out to construct an energy budget for juvenile thick lipped mullet, Crenimugil labrosus Risso. A partial factorial experimental design was used to examine the effects of temperature, fish size and meal size on growth. The maximum ration that the fish were able to ingest completely per day was found to be 0·8, 1·4 and 2·3% wet body weight (b.w.) at 13,18 and 23°C, respectively. Ingested maintenance requirements (M.R.) were estimated to be 137, 205 and 288 cal fish^-1 day^-1 at 13, 18 and 23°C, respectively. At 18deg; C, M.R. varied as 25 W^1.04 cal day^-1, where W= fish weight (g). Growth rate increased with increasing temperature. Maximal conversion efficiency was 21–24% and was achieved closer to the maximum ingested ration with increasing temperature. The relationship between respiration rate and W at 18deg; C for 3-20 g fish is described by: respiration rate (ml O₂ h^-1) = 0·128 W^0.976 The energy cost of apparent specific dynamic action at 18deg; C was found to vary between 5·1% and 23·6% of the calorific value of the ingested meal (1% wet b.w.) , mean (± S.E.)=10·2 ± 2·0%. Post mortem analyses of groups of fish fed 0·2, 0·8 and 1·5% wet b.w. meals showed a significant increase in total lipid and a significant decrease in water content with increasing ratio size. A negative correlation was found between body water content and total lipid (and calories). The mean assimilation efficiency (±s.e.) for 5–10 g mullet at 18deg; C was 73·9 ± 3·6%. The observations reported in this study were brought together to construct an energy budget for juvenile C. labrosus which was found to give a reliable prediction (within 10%) of energy demand and growth under the prevailing experimental conditions. Both gross (K₁) and net (K₂) growth efficiencies, based on energy values, increased with increasing ratio size up to satiation and were independent of temperature. The maximum values of K₁ and K₂ observed were 0·33 and 0·46, respectively. The third order efficiency (K₃) appeared to be independent of temperature and ration size; mean values ranged between 0·66 and 0·84.     

Physiological ecology of a tropical dragon,Lophognathus temporalis

Lophognathus temporalis is an arboreal lizard from the wet–dry tropics of Australia. During the wet season the field metabolic rate (FMR) of the lizards was 209 kJ kg^?1 d^?1, but during the dry season FMR was only 62 kJ kg^?1 d^?1. Similarly, water flux decreased from 73.6 mL kg^?1 d^?1 in the wet season to 18.5 mL kg^?1 d^?1 in the dry season. Body temperatures (T_b) were significantly lower in the dry season, and operative temperatures, calculated by incorporating microclimatic data with characteristics of the lizards, indicated that the seasonal shift was due to changes in thermoregulatory behaviour rather than limitations of the thermal environment. By combining field measurements of T_b and FMR with laboratory measurements of standard metabolic rate over a range of T_b, we were able to subdivide the FMR into its components and to determine which factors contributed to the seasonal reduction in energy expenditure. During the dry season, lizards used 147 kJ kg^?1 d^?1 less energy than during the wet season, and 24% of this decrease was estimated to be due to the passive effects of lower nighttime T_b, 14% was due to the active selection of lower daytime T_b, 27% was due to the physiological shift to lower standard metabolic rates, and 35% was due to reduced activity in the dry season. Although the population size remained relatively constant (107 lizards ha^?1 during the wet season and 125 lizards ha^?1 during the dry season), the population structure changed, reflecting the seasonal patterns of recruitment and mortality. The number of lizards active at any one time was much lower in the dry season, reflecting the lower levels of activity in this season. The energy expenditure of the population of L. temporalis was 612 kJ ha^?1 d^?1 during the wet season and 113 kJ ha^?1 d^?1 during the dry season.     

Postprandial metabolic increment of southern bluefin tuna Thunnus maccoyii ingesting high or low‐lipid sardines Sardinops sagax

This study examined the postprandial metabolism and swimming speed of southern bluefin tuna Thunnus maccoyii when fed sardines Sardinops sagax of either high‐lipid and high‐energy content or low‐lipid and low‐energy content. Five groups of two or three T. maccoyii (mean ±s.e. mass = 19·8 ± 0·5 kg, n = 14) were fed either low [2·2% lipid, 5·5 MJ kg^?1 gross energy (GE)] or high‐lipid (12·9%, 9·2 MJ kg^?1 GE) S. sagax. Before feeding, T. maccoyii swam at 0·74 ± 0·03 body lengths s^?1 (n = 5) and their routine metabolic rate was 305 ± 15 mg kg^?1 h^?1. Swimming speed and metabolic rate of T. maccoyii increased following feeding. Thunnus maccoyii swam 1·3 and 1·8 times faster during digestion of low and high‐lipid S. sagax, respectively. Postprandial peak metabolic rate, duration of elevated metabolism and total postprandial metabolic increment were all greater for T. maccoyii that ingested high‐lipid S. sagax. When total postprandial increment is represented as a proportion of ingested energy, there was no difference between high and low‐lipid meals, equating to between 30 and 35% of ingested energy. It was estimated that increased postprandial swimming costs account for 25 and 46% of the total postprandial metabolic response for low and high‐lipid S. sagax meals, respectively. Specific dynamic action (SDA) accounts for c. 20% of ingested energy regardless of S. sagax lipid level. These results confirm that the postprandial metabolic increment of T. maccoyii is greater than most other fish species. Much of the high cost of postprandial metabolic increment can be attributed to increased postprandial swimming costs. For T. maccoyii, it appears that activity and SDA are not independent, which complicates bioenergetic evaluation. High postprandial metabolic costs accentuate the great energetic requirements of T. maccoyii.     

Contrasts in energy intake and expenditure in sit-and-wait and widely foraging lizards

Summary Daily energy metabolism and water flux were measured with doubly labeled water in the free-living insectivorous lizards Cnemidophorus tigris (mean body mass 15.7 g) and Callisaurus draconoides (8.6 g) in June 1979 in the Colorado Desert of California. C. tigris was an active forager; it spent 91% of its 5-h daily activity period in movement. C. draconoides was a sit-and-wait predator; it spent less than 2% of its 10-h activity period in movement. C. tigris had significantly higher rates of field energy metabolism and water influx (210 Jg^-1 day^-1, 36.8 ul H₂O g^-1 day^-1, N=19) than C. draconoides (136, 17.1, N=18). There were no significant differences between the sexes within either species.The extra costs of free existence were calculated from differences between field metabolic rates and maintenance costs estimated from laboratory respirometry. Rates of energy metabolism during the field activity period were about 1.5x resting levels at 40° C (field active body temperature) for C. draconoides and 3.3 x resting levels at 40° C (field active body temperature) for the more active C. tigris. Feeding rates calculated from water influx data were 13.3 mg g^-1 day^-1 for C. tigris and 5.8 mg g^-1 day^-1 for C. draconoides. Though C. tigris had a high rate of energy expenditure, its foraging efficiency was higher than C. draconoides'.     

Three decades of longlining in Bimini,Bahamas, reveals long‐term trends in lemon shark Negaprion brevirostris (Carcharhinidae) catch per unit effort

In Bimini, Bahamas, the consistent employment of longlines, beginning in 1982, provided a rare opportunity to explore population trends for large resident sharks. This study assessed three shallow water longline survey periods at this location; 1982–1989, 1992–2002 and 2003–2014, with the aim of determining trends in annual catch per unit effort (CPUE) for an IUCN listed near‐threatened species, the lemon shark Negaprion brevirostris. A general additive model (GAM) was used to analyse the non‐linear annual CPUE values over the entire 32‐year research period. The GAM displayed high variability of annual CPUE, with a peak value of 0·026 N. brevirostris per hook day (hooks day^?1) in 2000. The temporal pattern of CPUE indicated an abundance trend with a complete cycle, from trough to trough, occurring over a period of approximately 18 years. The 1982–1989 survey period saw the highest proportion of mature individuals (19·8%) and the smallest average pre‐caudal length (L_PC; 124·8 cm). The 1992–2002 survey period had the highest average annual CPUE (0·018 hooks day^?1), while the 2003–2014 research period saw largest average L_PC size (134·8 cm) and the lowest average CPUE values (0·009 hooks day^?1) of the entire research period. The long‐term trend identified in this study provides a baseline for future assessment.     

Growth and Production of Yellow Eels and Glass Eels in Ponds

Two experiments (I and II) were performed in drainable ponds. Yellow eels Anguilla anguilla (L.) were stocked in early June at three biomasses: 10, 20 and 60 kg · ha⁻¹ in experiment I; and 10, 20 and 40 kg · ha⁻¹ in experiment II. The mean body weights were 27.0 and 24.2 g respectively. Glass eels were stocked only in experiment II at equal densities of 1600·ha⁻¹. In both experiments each biomass of yellow eel was combined in a factorial design with three cyprinid communities differing in biomass and in species- and size-composition. The ponds were drained in autumn. The final body weights at draining ranged from 25.9 to 63.6 g for yellow eel and from 3.9 to 8.8 g for glass eel. The final body weights of yellow eel and of glass eel decreased with increasing biomass of yellow eel. No significant relation was found between the bream Abramis brama (L.) biomass and the growth of eel. The growth rates of yellow eel and glass eel were positively correlated in experiment II. At higher biomasses of yellow eel the percentage females decreased slightly. The recapture rates of yellow eel in experiments I and II amounted to 69.4 ± 9.8 % and 92.2 ± 4.9% (mean ± sd) respectively. The lower recapture rates in experiment I were caused by the inappropriate draining technique used. The glass eels were recaptured with 75.0·5.6% efficiency. The maximum net production of yellow eel occurred at a biomass of 20–40kg·ha⁻¹ and amounted to 19 kg·ha⁻¹.     

Sexual dimorphism in the energetics of reproduction and growth of North Sea plaice, Pleuronectes platessa L.

The chemical composition and energy content of North Sea plaice during the spawning period were examined in mature males and females and in immature fish, to study differences in the allocation of energy over reproduction and somatic growth between the sexes. At the beginning of the spawning period mature males and females had equal dry weights of lipid that were 70% higher than in immatures. Protein content in mature males was equal to that in immatures but was 23 % higher in mature females. Immature males and females did not differ in chemical composition. At the end of the spawning period, spent and immature fish had equal lipid contents, but protein content in spent females was 10% lower than in spent males, and 17% lower than in immatures. Gross energy content of the body decreased by 44% (65·2 to 36·3 J cm^-3) in mature females, 27% (55·0 to 40·OJ cm^-3) in mature males, and 9% (48·7 to 44·2J cm^-3) in immatures. Energy content of plaice eggs was estimated at 6·60 kJ per 1000 eggs. Reproductive investment was estimated from the energy loss during the spawning period and included the energy of sex products and spawning metabolism. Somatic growth comprised the annual increase in energy content of fish. The pattern of energy allocation over reproduction and somatic growth differed between males and females. Males started their reproduction at a smaller length and a younger age and allocated a higher proportion of the available energy into reproduction than females. Available energy resources for somatic growth and reproduction (surplus production) were equal between the sexes up to a length of about 30 cm. Beyond this length male surplus production levelled off whereas female surplus production continued to increase. The differences in surplus production and the allocation patterns are discussed. For female plaice the energy allocated into egg production was estimated as between 48 and 64% of the total amount of energy lost during spawning. The remaining energy is used for metabolism during the spawning period, yielding an estimate of the metabolic rate of mature females of between 6·4 and 9·1 kJ day^-1. A maximum estimate of the metabolic rate of mature males was 7·4 kJ day^-1.     

Physiological ecology of frillneck lizards in a seasonal tropical environment

The frillneck lizard, Chlamydosaurus kingii, is a conspicuous component of the fauna of the wetdry tropics of northern Australia during the wet season, but it is rarely seen in the dry season. Previous studies have demonstrated that during the dry season the field metabolic rate (FMR) is only about one-quarter of the wet-season rate, and one factor involved in this seasonal drop is a change in the behavioural thermoregulation of the species such that lower body temperatures (T _bs) are selected during dry-season days. Here we examine other factors that could be responsible for the seasonal change in FMR: standard metabolic rates (SMR) and activity. Samples from stomach flushing revealed that the lizards in the dry season continued to feed, but the volume of food was half as much as in the wet season. SMR in the laboratory was 30% less in the dry season. During the dry season, the energy expended by the lizards is 60.4 kJ kg^-1 day^-1 less than during the wet season. Combining laboratory and field data, we determined the relative contribution of the factors involved in this energy savings: 10% can be attributed to lower nighttime T _b, 12% is attributable to lower daytime T _b, 12% is attributable to decreased metabolism, and the remaining 66% is attributable to other activities (including e.g. locomotion, reproductive costs, digestion). Calculations indicate that if FMR did not drop in the dry season the lizards would not survive on the observed food intake during this season. Seasonal analysis of blood plasma and urine indicated an accumulation of some electrolytes during the dry season suggesting modest levels of water stress.