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The endemic angiosperm Posidonia oceanica plays a remarkable role as marine habitat and ecosystem service provider in shallow waters in the Mediterranean Basin through their vertical growth, oxygenation of the water column and as a carbon sink storing allochthonous carbon and biomass underneath the meadows. Here we assess the capacity of a pristine meadow at 8m depth in the PMNT Cabrera (Mallorca, Spain) to oxygenate the water column in the coastal area through monitoring of oxygen concentrations and subsequent evaluation of the metabolic rates from these profiles in the benthic as well as pelagic compartment. Here we report dissolved oxygen (DO) measurements from a CT at 4m dept with continuous (hourly) measurements from October 2019 to October 2021 as well as DO measurements from multiparameteric sensors in the meadow (8m depth) during some weeks in the same period and 2 evalautions of DO with closed incubations.

The red swamp crayfish (Procambarus clarkii) is the most widely spread freshwater crayfish worldwide. Competing physiological traits can influence invasion success in any given environment by limiting the available scope for aerobically demanding activities. While high flows have been associated with reduced crayfish movement upstream, the effects of flow alteration on their metabolic demands have been largely overlooked. In this study, we estimated routine metabolic rate (RMR) at rest and oxygen consumption rates of crayfish under different current velocities in a flume respirometer, while maximum metabolic rate (MMR) was determined using the exhaustive chase protocol. We also measured some morphometric variables in males and females of crayfish. Oxygen uptake substantially increased with crayfish size and current velocity due to increased energy expenditure to overcome drag and hold a stationary position. Sexual dimorphism in morphological traits did not lead to sexual differences in oxygen uptake. Moreover, we found that individuals operated close to their maximum aerobic capacity at elevated current velocities (≥ 25 cm s− 1). This suggested that the high flow-driven energetic demand may compromise the energy available for reproduction, growth and dispersal, thereby affecting overall fitness. These metabolic constraints could partly explain the failed invasions of invasive crayfish in fast-flowing waters.

The data is a compilation of information on metabolic rates of Mediterranean seagrasses obtained by two different methodologies (benthic incubations and multiparametric sensors) from published literature and data from the authors.

At marine methane seeps, vast quantities of methane move through the shallow subseafloor, where it is largely consumed by microbial communities. This process plays an important role in global methane dynamics, but we have yet to identify all of the methane sinks in the deep sea. Here, we conducted a continental-scale survey of seven geologically diverse seafloor seeps and found that carbonate rocks from all sites host methane-oxidizing microbial communities with substantial methanotrophic potential. In laboratory-based mesocosm incubations, chimney-like carbonates from the newly described Point Dume seep off the coast of Southern California exhibited the highest rates of anaerobic methane oxidation measured to date. After a thorough analysis of physicochemical, electrical, and biological factors, we attribute this substantial metabolic activity largely to higher cell density, mineral composition, kinetic parameters including an elevated Vmax, and the presence of specific microbial lineages. Our data also suggest that other features, such as electrical conductance, rock particle size, and microbial community alpha diversity, may influence a sample's methanotrophic potential, but these factors did not demonstrate clear patterns with respect to methane oxidation rates. Based on the apparent pervasiveness within seep carbonates of microbial communities capable of performing anaerobic oxidation of methane, as well as the frequent occurrence of carbonates at seeps, we suggest that rock-hosted methanotrophy may be an important contributor to marine methane consumption.

At marine methane seeps, vast quantities of methane move through the shallow subseafloor, where it is largely consumed by microbial communities. This process plays an important role in global methane dynamics, but we have yet to identify all of the methane sinks in the deep sea. Here, we conducted a continental-scale survey of seven geologically diverse seafloor seeps and found that carbonate rocks from all sites host methane-oxidizing microbial communities with substantial methanotrophic potential. In laboratory-based mesocosm incubations, chimney-like carbonates from the newly described Point Dume seep off the coast of Southern California exhibited the highest rates of anaerobic methane oxidation measured to date. After a thorough analysis of physicochemical, electrical, and biological factors, we attribute this substantial metabolic activity largely to higher cell density, mineral composition, kinetic parameters including an elevated Vmax, and the presence of specific microbial lineages. Our data also suggest that other features, such as electrical conductance, rock particle size, and microbial community alpha diversity, may influence a sample's methanotrophic potential, but these factors did not demonstrate clear patterns with respect to methane oxidation rates. Based on the apparent pervasiveness within seep carbonates of microbial communities capable of performing anaerobic oxidation of methane, as well as the frequent occurrence of carbonates at seeps, we suggest that rock-hosted methanotrophy may be an important contributor to marine methane consumption.

Atlantic bluefin tuna is an emblematic scombrid species, but many physiological aspects during the larval stages are still unknown. The mechanisms of how fish larvae balance growth and activity are of great interest since metabolic costs are very high compared to juveniles and adults. However, there is a lack of information about metabolic costs in scombrid larvae. This lack of data is probably related to the challenges associated to larval handling before and during respirometry trials. In this study for the first time, we: i) estimate the relationship between routine metabolic rate and the larval dry weight (mass scaling exponent) at 26°C, ii) measure metabolism under light and darkness and iii) explore the influence of nutritional status (RNA:DNA ratio) on the inter-individual variability in metabolic rates. The relationship between metabolism and size (ranging from 0.6 to 23 mg) was near isometric (slope, b=0.99), in contrast to the allometric relationship observed in most species (b=0.87). Our results show no significant differences in oxygen consumption under light and darkness. A possible regulation (decrease) of their swimming activity with the consequent decrease in the oxygen consumption in light situations is discussed. Nutritional condition did not explain the inter-individual differences in oxygen consumption. This study first reports metabolic rates of Atlantic bluefin tuna larvae and discusses the challenges of performing bioenergetics studies with early life stages of Scombrids.

The proposed work has two objectives to improve prediction and assessment capabilities. The first objective is to determine if the generalized equation provided by our new gait mechanics model predicts the metabolic cost of weighted and unweighted walking more accurately than existing generalized equations. Our second objective is to determine how accurately weighted and unweighted walking metabolic rates can be estimated in field settings from simple technologies. Metabolic rates will be measured from expired gases. The timing of each walking stride, as well as its subcomponents (i.e. the contact and leg swing portions) will be determined from video. In addition, the periods of muscular activity responsible for executing the movements of the walking stride will be also assessed from electrical activity using surface electrodes attached to the skin above target muscles. The forces that subjects apply to the ground during locomotion may be measured from either a force plate or force sensors built into a treadmill. Finally, heart rate monitors to measure heart beat frequency, miniature motion sensors mounted to the shoe or other parts of the body to measure movement speeds and rates may also be utilized.

For Atlantic salmon (Salmo salar) and brown trout (Salmo trutta), the decision to migrate or when to migrate is believed to be influenced by the individual’s metabolic rate (MR) relative its food intake. As MR was expected to be related to behaviour, the potential links between behaviour and metabolic costs was studied. For both salmon and trout the dominant individual had a higher standard metabolic rate (SMR) than its subordinate counterpart. Also, successful migrants of brown trout had a higher SMR than unsuccessful migrants, whereas no such difference was found for obligate migratory Atlantic salmon. Measures of variation in MR and boldness indicated that Atlantic salmon was more sensitive to stress than brown trout and became passive when stressed. When two trout were interacting, an increase in ventilation rate (VR) was positively correlated to fighting intensity. The first day after an interaction, VR did not differ between small dominant and subordinate trout (mean size 3.7g), whereas for large trout (26.0g) subordinates had higher VR than dominants. However, a combination of low temperature (10°C) and high water velocity (22cm/s) eliminated this difference. This probably reflects the high swimming activity of small dominants and the low motivation for dominants to defend a large territory when temperatures were low and the cost of moving was high. These results show that the relationship between MR and behaviour may differ depending on species, fish size and environmental factors.

For Atlantic salmon (Salmo salar) and brown trout (Salmo trutta), the decision to migrate or when to migrate is believed to be influenced by the individual’s metabolic rate (MR) relative its food intake. As MR was expected to be related to behaviour, the potential links between behaviour and metabolic costs was studied. For both salmon and trout the dominant individual had a higher standard metabolic rate (SMR) than its subordinate counterpart. Also, successful migrants of brown trout had a higher SMR than unsuccessful migrants, whereas no such difference was found for obligate migratory Atlantic salmon. Measures of variation in MR and boldness indicated that Atlantic salmon was more sensitive to stress than brown trout and became passive when stressed. When two trout were interacting, an increase in ventilation rate (VR) was positively correlated to fighting intensity. The first day after an interaction, VR did not differ between small dominant and subordinate trout (mean size 3.7g), whereas for large trout (26.0g) subordinates had higher VR than dominants. However, a combination of low temperature (10°C) and high water velocity (22cm/s) eliminated this difference. This probably reflects the high swimming activity of small dominants and the low motivation for dominants to defend a large territory when temperatures were low and the cost of moving was high. These results show that the relationship between MR and behaviour may differ depending on species, fish size and environmental factors.

For Atlantic salmon (Salmo salar) and brown trout (Salmo trutta), the decision to migrate or when to migrate is believed to be influenced by the individual’s metabolic rate (MR) relative its food intake. As MR was expected to be related to behaviour, the potential links between behaviour and metabolic costs was studied. For both salmon and trout the dominant individual had a higher standard metabolic rate (SMR) than its subordinate counterpart. Also, successful migrants of brown trout had a higher SMR than unsuccessful migrants, whereas no such difference was found for obligate migratory Atlantic salmon. Measures of variation in MR and boldness indicated that Atlantic salmon was more sensitive to stress than brown trout and became passive when stressed. When two trout were interacting, an increase in ventilation rate (VR) was positively correlated to fighting intensity. The first day after an interaction, VR did not differ between small dominant and subordinate trout (mean size 3.7g), whereas for large trout (26.0g) subordinates had higher VR than dominants. However, a combination of low temperature (10°C) and high water velocity (22cm/s) eliminated this difference. This probably reflects the high swimming activity of small dominants and the low motivation for dominants to defend a large territory when temperatures were low and the cost of moving was high. These results show that the relationship between MR and behaviour may differ depending on species, fish size and environmental factors.

For Atlantic salmon (Salmo salar) and brown trout (Salmo trutta), the decision to migrate or when to migrate is believed to be influenced by the individual’s metabolic rate (MR) relative its food intake. As MR was expected to be related to behaviour, the potential links between behaviour and metabolic costs was studied. For both salmon and trout the dominant individual had a higher standard metabolic rate (SMR) than its subordinate counterpart. Also, successful migrants of brown trout had a higher SMR than unsuccessful migrants, whereas no such difference was found for obligate migratory Atlantic salmon. Measures of variation in MR and boldness indicated that Atlantic salmon was more sensitive to stress than brown trout and became passive when stressed. When two trout were interacting, an increase in ventilation rate (VR) was positively correlated to fighting intensity. The first day after an interaction, VR did not differ between small dominant and subordinate trout (mean size 3.7g), whereas for large trout (26.0g) subordinates had higher VR than dominants. However, a combination of low temperature (10°C) and high water velocity (22cm/s) eliminated this difference. This probably reflects the high swimming activity of small dominants and the low motivation for dominants to defend a large territory when temperatures were low and the cost of moving was high. These results show that the relationship between MR and behaviour may differ depending on species, fish size and environmental factors.

The proposed work has two objectives to improve prediction and assessment capabilities. The first objective is to determine if the generalized equation provided by our new gait mechanics model predicts the metabolic cost of weighted and unweighted walking more accurately than existing generalized equations. Our second objective is to determine how accurately weighted and unweighted walking metabolic rates can be estimated in field settings from simple technologies. Metabolic rates will be measured from expired gases. The timing of each walking stride, as well as its subcomponents (i.e. the contact and leg swing portions) will be determined from video. In addition, the periods of muscular activity responsible for executing the movements of the walking stride will be also assessed from electrical activity using surface electrodes attached to the skin above target muscles. The forces that subjects apply to the ground during locomotion may be measured from either a force plate or force sensors built into a treadmill. Finally, heart rate monitors to measure heart beat frequency, miniature motion sensors mounted to the shoe or other parts of the body to measure movement speeds and rates may also be utilized., The original document contains color images.

Adult specimens of two species of clams, Ruditapes decussatus and Venerupis pullastra, were starved for 84 days to determine the effect of starvation on their metabolism. The energy cost of metabolism in starvation was assessed using the oxygen consumption rates (respiration rates) of the clams and assessing the type of fuel used to provide this energy by analyzing their biochemical composition. Respiration rates decreased in both species after 15 days of starvation and remained at basal levels throughout the rest of the experimental period. Both during the first period and also after the metabolism had slowed down, the amount of energy consumed in respiration was higher in V. pullastra than in R. decussatus. The energy needed to maintain vital functions in both species is obtained from catabolism of body components, with a reduction in dry mass of the specimens, and consequently their energy content, in both species. This reduction was greater in V. pullastra given that energy demand is higher in this species. In both species carbohydrates made the largest contributions to energy output, followed by lipids in males and proteins in females. However, the energy contribution of each biochemical component differs according to species: R. decussatus obtains its energy from the catabolism of carbohydrates and proteins in equal proportion, while V. pullastra obtains it from proteins and lipids. In both species, albeit to a greater extent in R. decussatus, we observed that female specimens conserved their lipids until the later stages of the period of starvation (day 70), after which they started to metabolise their lipid components more intensely. The interspecific differences are interpreted in relation to the different habitat occupied by the two species

Although the amount of energy that males and females invest in reproduction is an integral component of theories explaining the evolution of particular mating strategies, few studies have actually determined the amount of energy that each sex allocates to reproduction. We compared how energy is expended by male and female Anolis carolinensis lizards during both the breeding and postbreeding seasons. We used laboratory respirometry to determine resting metabolic rates (RMRs) of inactive, freshly captured lizards and the doubly labeled water technique to determine field metabolic rates (FMRs) of free-ranging lizards. Both RMRs and FMRs were influenced by body mass but not by sex. Season did not influence FMRs; however, RMRs of both sexes increased similar to 40% from the breeding to the postbreeding season. The seasonal increase in RMRs was attributed to a postreproductive increase in feeding rate and specific dynamic action. We used RMRs, FMRs, and thermal profiles of lizards to calculate energy budgets for breeding and postbreeding seasons. Energy budgets partitioned daily field energy (DFE; calculated from FMRs) into daily activity energy ( DAE) and daily resting energy (DRE; calculated from RMRs). Energy expended for reproduction was estimated as DAE during the breeding season plus egg production ( for females). Despite males having 40% greater body mass, females expended 46% more energy for reproduction than did males ( 906 and 619 J/d, respectively). Total metabolizable energy (TME = production for females) expended during the breeding season was similar for males and females ( 1,280 and 1,365 J/d, respectively). Although TME of females decreased 44% from the breeding to the postbreeding season ( 1,365 vs. 766 J/ d), TME of males was similar during both seasons ( 1,280 vs. 1,245 J/ d). There were both seasonal and sexual differences in DRE and DAE. Compared with most lizards from semiarid/ desert habitats, A. carolinensis in a temperate habitat expends more tota

Although the amount of energy that males and females invest in reproduction is an integral component of theories explaining the evolution of particular mating strategies, few studies have actually determined the amount of energy that each sex allocates to reproduction. We compared how energy is expended by male and female Anolis carolinensis lizards during both the breeding and postbreeding seasons. We used laboratory respirometry to determine resting metabolic rates (RMRs) of inactive, freshly captured lizards and the doubly labeled water technique to determine field metabolic rates (FMRs) of free-ranging lizards. Both RMRs and FMRs were influenced by body mass but not by sex. Season did not influence FMRs; however, RMRs of both sexes increased similar to 40% from the breeding to the postbreeding season. The seasonal increase in RMRs was attributed to a postreproductive increase in feeding rate and specific dynamic action. We used RMRs, FMRs, and thermal profiles of lizards to calculate energy budgets for breeding and postbreeding seasons. Energy budgets partitioned daily field energy (DFE; calculated from FMRs) into daily activity energy ( DAE) and daily resting energy (DRE; calculated from RMRs). Energy expended for reproduction was estimated as DAE during the breeding season plus egg production ( for females). Despite males having 40% greater body mass, females expended 46% more energy for reproduction than did males ( 906 and 619 J/d, respectively). Total metabolizable energy (TME = production for females) expended during the breeding season was similar for males and females ( 1,280 and 1,365 J/d, respectively). Although TME of females decreased 44% from the breeding to the postbreeding season ( 1,365 vs. 766 J/ d), TME of males was similar during both seasons ( 1,280 vs. 1,245 J/ d). There were both seasonal and sexual differences in DRE and DAE. Compared with most lizards from semiarid/ desert habitats, A. carolinensis in a temperate habitat expends more tota

It is of interest to investigate the possible effect of a new synthetic steroid, Aldactone, on the total body weight of the rodent Dipodomys. In addition, the present study includes the effect of dehydration and of high salt intake on the oxygen consumption of the Dipodomys, in a resting state.

It is of interest to investigate the possible effect of a new synthetic steroid, Aldactone, on the total body weight of the rodent Dipodomys. In addition, the present study includes the effect of dehydration and of high salt intake on the oxygen consumption of the Dipodomys, in a resting state.