Dynamics of body mass and oxygen consumption in the ribbed newt <Emphasis Type="Italic">Pleurodeles waltl</Emphasis> ontogenesis: 1. Endotrophic development

The correlation between parameters of growth and energy metabolism in the example of embryonic and larval development of the ribbed newt Pleurodeles waltl has been studied. The wet body mass increases five times during this period due to water absorption by developing tissues and the yolk, and the dry mass decreases 1.18 times. The highest mass-specific growth rate and mass-specific rate of oxygen consumption of developing tissues was noticed at the 33rd stage of embryogenesis (13th–14th day of development). These indexes decreased after the hatching, but increased after larvae switched to external nutrition. Comparison of the studied parameters has identified a similar features in alteration of mass-specific growth rate, mass-specific rate of oxygen consumption, and watering of developing tissues in early development of the ribbed newt.     

The development of thermoregulation in turkey and guinea fowl hatchlings: similarities and differences

The development of thermoregulation was studied in turkeys (Meleagris gallopavo, 60.5 g) and guinea fowl (Numida meleagris, 33.5 g) from 2 to 24 h after hatching. Thermoregulation was measured at different ages during 1 h of cold exposure (20°C). Final body temperature rose linearly with age in turkeys, but reached a plateau in guinea fowl between 12 and 16 h. At 2 h after hatch final body temperature was highest in guinea fowl, while at 24 h after hatch there was no difference between the species. The development of mass-specific metabolic rate with age resembled the pattern of final body temperature. At 2 h post-hatch mass-specific metabolic rate was highest in guinea fowl; however, at 24 h post-hatch there was no difference between the species. since mass-specific metabolic rate reached a plateau in guinea fowl at 16 h. In turkeys mass-specific dry thermal conductance decreased with age initially, while in guinea fowl it remained stable. Nevertheless, at both 2 and 24 h after hatch mass-specific wet conductance did not differ significantly between the species. In turkeys mass-specific wet conductance increased initially. This increase in mass-specific wet conductance may be due to the rapid onset of feather growth in turkeys. The O₂ consumption per breath doubled during the first 24 h in turkeys but remained stable in guine fowl. This suggests that at least two different developmental patterns of O₂ intake exist within Galliformes. The results show that 2 h post-hatch the thermoregulatory ability was lowest in turkeys, despite their larger body mass. However, at 24 h post-hatch the difference between the species was not significant, because the thermoregulatory ability had increased more in turkeys.Abbreviations B _f breathing frequency - BM body mass - BMR basal metabolic rate - C _D mass-specific dry thermal conductance - C _w mass-specific wet thermal conductance - HI homeothermy index - H _E evaporative heat loss - H _B loss of stored body heat - MR metabolic rate - M _MS mass-specific metabolic rate - RH relative humidity - I _A ambient temperature - T _Bi initial body temperature - T _Bf final body temperature - VO₂ volume oxygen consumed - VCO₂ volume carbon dioxide produced     

Dynamics of energy metabolism in ontogenesis of striped shield bug (<Emphasis Type="Italic">Graphosoma lineatum</Emphasis> L.) and cabbage moth (<Emphasis Type="Italic">Mamestra brassicae</Emphasis> L.)

Dynamics of growth and oxygen consumption during ontogenesis of insects with direct (striped shield bug Graphosoma lineatum L.) and indirect (cabbage moth Mamestra brassicae L.) development have been compared. The correlation between a character of energy metabolism alteration and peculiarities of development of the insects has been shown. Cyclic decrease of oxygen consumption during molt and sharp dropping during metamorphosis have been observed in insects with indirect development. The decrease of oxygen consumption has been observed in insects with direct development only during molts. The coefficient a of allometric dependence of oxygen consumption on body weight of imago for cabbage moth was two times higher than that for striped shield bug.     

Standard Metabolic Rate in Gastropoda Class

Abstarct—The relationship between oxygen consumption and soft tissue weight in the Gastropoda class (according to the obtained and published data) is expressed by the equation with coefficientsa = 0.71 and k = 0.78. Prosobranch and pulmonate snails have similar levels of oxygen consumption. Opisthobranch snails have higher oxygen consumption. No relationship has been revealed between the metabolic rate (coefficient a) and climatic zone of the gastropod habitat.     

Age-Related Changes in Oxygen Consumption in the Edible Mussel <Emphasis Type="Italic">Mytilus edulis</Emphasis> from the White Sea

We determined the rate of oxygen consumption in the White Sea edible mussel Mytilus edulis of different ages. The mass-specific rate of oxygen consumption proved to decrease with mussel age according to the equation: = 40.1/(1 – e ^–0.194t ), where is mass-specific rate of oxygen consumption and t is age. Allometric coefficients of the oxygen consumption rate–soft tissue weight relationship were also determined.     

Effect of Temperature on the Rate of Oxygen Consumption during the Second Half of Embryonic and Early Postembryonic Development of European Pond Turtle <Emphasis Type="Italic">Emys orbicularis</Emphasis> (Reptilia: Emydidae)

Oxygen consumption by eggs of European pond turtle was determined at two constant incubation temperatures of 25 and 28°C during the second half of embryogenesis. During development at both temperatures, the rate of oxygen consumption initially increased to remain constant during the last quarter of embryogenesis. The difference between the rates of oxygen consumption at these temperatures decreased during the studied period. The coefficient Q₁₀ for the rate of oxygen consumption decreased from 9 to 1.7. At an incubation temperature of 28°C, the changes in the rate of oxygen consumption in response to a short-term temperature decrease to 25°C or increase to 30°C depended on the developmental stage and were most pronounced at the beginning of the studied period. During late embryonic and first 2.5 months of postembryonic development, the rate of oxygen consumption did not significantly differ after such temperature changes. The regulatory mechanisms formed during embryonic development are proposed to maintain the level of oxygen consumption during temperature changes.     

Energetic metabolism during individual development of <Emphasis Type="Italic">Lymnaea stagnalis</Emphasis> (Lymnaeidae,gastropoda): III. Late postlarval ontogeny

Changes in the rate and intensity of oxygen consumption during individual ontogeny of 14 specimens of Lymnaea stagnalis in the period from the 10th week after emergence until death was investigated in aquaculture. It was demonstrated that the rate of oxygen consumption increased and the intensity of this process decreased during the whole period of observations. Alterations of these parameters were accompanied with permanent oscillations of their meanings. The correlation between intensity of oxygen consumption (q) and age (t) can be described with the equation q = q _st/(1-exp(−k _g (t+t ₀))). The values of coefficients of this equation do not differ significantly between individuals and, on average, comprise k _g = 0.0696 ± 0.0072 weeks⁻¹; q _st = 60.4 ± 2.6 mcl O₂/(h · g); t ₀ = −3.0 ± 0.7 weeks. The dependence of the rate of oxygen consumption (Q, μl O₂/h) on body weight (M, g) for all data is significantly described with the allometric equation Q = 0.369M ^0.779.     

Oxygen consumption and ammonia excretion rates in Octopus maya,loligo forbesi and Lolliguncula brevis (Mollusca: Cephalopoda)

Oxygen consumption and ammonia excretion rates were investigated in young Octopus maya (hatching to 139 days old; 0.11–81.23 g wet body weight, BW; 22.5–23.9°C), young squids of Loligo forbesi (hatching to 45 days old; 9.4–115.3 mg BW; 12.3–13.1°C) and young squids of Lolliguncula brevis (2.00–39.98 g BW; 23.8–24.7°C). Except at hatching, oxygen consumption and ammonia excretion rates on an individual basis (M) of these three cephalopods increased linearly with increasing body weight (BW) expressed as M = aBW^b . Values of b for oxygen consumption were 0.900, 0.910 and 0.848 and for ammonia excretion were 0.744, 0.809 and 0.751 for O. maya, L. forbesi and L. brevis, respectively. Among the three species the value a varied widely, while b was similar for both oxygen consumption and ammonia excretion rates. Based upon these data, metabolism for hatchlings of O. maya and L. forbesi was estimated to be relatively lower than that of older juveniles. The O/N ratios for hatchlings of O. maya and L. forbesi were relatively high and indicate an apparent dependence upon lipids in the immediate post‐hatching period, followed by standard protein energy utilization thereafter.     

Intermolt development reduces oxygen delivery capacity and jumping performance in the American locust (<Emphasis Type="Italic">Schistocerca americana</Emphasis>)

Among animals, insects have the highest mass-specific metabolic rates; yet, during intermolt development the tracheal respiratory system cannot meet the increased oxygen demand of older stage insects. Using locomotory performance indices, whole body respirometry, and X-ray imaging to visualize the respiratory system, we tested the hypothesis that due to the rigid exoskeleton, an increase in body mass during the intermolt period compresses the air-filled tracheal system, thereby, reducing oxygen delivery capacity in late stage insects. Specifically, we measured air sac ventilation frequency, size, and compressibility in both the abdomen and femur of early, middle, and late stage sixth instar Schistocerca americana grasshoppers. Our results show that late stage grasshoppers have a reduced air sac ventilation frequency in the femur and decreased convective capacities in the abdomen and femur. We also used X-ray images of the abdomen and femur to calculate the total proportion of tissue dedicated to respiratory structure during the intermolt period. We found that late stage grasshoppers had a lower proportion of their body dedicated to respiratory structures, especially air sacs, which convectively ventilate the tracheal system. These intermolt changes make oxygen delivery more challenging to the tissues, especially critical ones such as the jumping muscle. Indeed, late stage grasshoppers showed reduced jump frequencies compared to early stage grasshoppers, as well as decreased mass-specific CO₂ emission rates at 3 kPa PO₂. Our findings provide a mechanism to explain how body mass changes during the intermolt period reduce oxygen delivery capacity and alter an insect’s life history.     

The energy cost of embryonic development in fishes and amphibians,with emphasis on new data from the Australian lungfish, <Emphasis Type="Italic">Neoceratodus forsteri</Emphasis>

The rate of oxygen consumption throughout embryonic development is used to indirectly determine the ‘cost’ of development, which includes both differentiation and growth. This cost is affected by temperature and the duration of incubation in anamniote fish and amphibian embryos. The influences of temperature on embryonic development rate, respiration rate and energetics were investigated in the Australian lungfish, Neoceratodus forsteri, and compared with published data. Developmental stage and oxygen consumption rate were measured until hatching, upon which wet and dry gut-free masses were determined. A measure of the cost of development, the total oxygen required to produce 1 mg of embryonic dry tissue, increased as temperature decreased. The relationship between the oxygen cost of development (C, ml mg⁻¹) and dry hatchling mass (M, mg) in fishes and amphibians is described by C = 0.30 M^{0.22 ± 0.13 (95% CI)}, r ² = 0.52. The scaling exponent indicates that the cost of embryonic development increases disproportionally with increasing hatchling mass. At 15 and 20°C, N. forsteri cost of development is significantly lower than the regression mean for all species, and at 25°C is lower than the allometrically scaled data set. Unexpectedly, incubation of N. forsteri is long, despite natural development under relatively warm conditions, and may be related to a large genome size. The low cost of development may be associated with construction of a rather sluggish fish with a low capacity for aerobic metabolism. The metabolic rate is lower in N. forsteri hatchlings than in any other fishes or amphibians at the same temperature, which matches the extremely low aerobic metabolic scope of the juveniles.     

The dynamics of mass growth and oxygen consumption in ontogenesis of the newt <Emphasis Type="Italic">Pleurodeles waltl</Emphasis>: 3. The postlarval period

The relationship between animal growth and oxygen consumption was studied by the example of the postlarval period in ontogenesis of the newt Pleurodeles waltl. These parameters increased during the first 1.5 years after metamorphosis and then did not change. Gender differences were found for the body mass, growth rate, and rate of oxygen consumption, which in males were less than in females. The mass-specific rates of oxygen consumption in males and females were the same. The relationship between the body mass and the rate of oxygen consumption in immature and mature newts can be expressed by a common allometric equation.     

Dynamics of body mass and oxygen consumption in the ontogeny of the Spanish ribbed newt (<Emphasis Type="Italic">Pleurodeles waltl</Emphasis>): 2. Larval stage

The correlation between characteristics of growth and energy metabolism during the larval stage of development of the Spanish ribbed newt (Pleurodeles waltl) has been studied. During this period, its body mass is found to increase 140 times and the oxygen consumption rate, 77 times. The highest rate of specific body mass increase and oxygen consumption rate are noted in the early larval stage. Later, these characteristics decrease except for a brief period before completion of metamorphosis when the rate specific body mass increase rises. Comparison of the studied characteristics allows us to note a similar pattern in changes of the specific growth rate and the oxygen consumption rate during the premetamorphic development of the Spanish ribbed newt.     

Early development and allometric growth patterns in ide Leuciscus idus (Linnaeus 1758)

Allometric growth and ontogeny were studied in ide Leuciscus idus (L.) reared in laboratory conditions from 0 to 30 days post hatching (DPH), to define important steps in the species’ early life history. Based on the external morphology, eleven different stages during the early development of ide were identified (ES9_a – JS1_a; ES – embryonic stage, JS – juvenile stage). After a short period of rest, hatched individuals were visual feeders with a pelagic life. Organogenesis and allometric changes indicated that development priorities concerned feeding efficiency, respiration efficiency and locomotion performances. Also concluded was that the gradual changes observed in body proportions (which occurred across a wide range of body lengths) reflect the absence of abrupt changes in the behaviour and habitat and may also be considered as a gradual adaptation to life in flowing water.     

Vergleich von Messungen des kLa-Wertes nach der stationären und der dynamischen Methode bei der Fermentation von L-Lysin und Turimycin

The calculation and scale-up of fermentation processes need k_La as one of the most important engineering data. There are two methods to determine k_La depending on power input, aeration rate and the properties of the fermentation broth: static with a balance between air supply and exit, dynamic gassing out with following the changes of dissolved oxygen concentration during periods of air off and a following air on. Within early intervals of fermentation time the data from both methods agree well, while for later time intervals the dynamic method always gives much lower values for k_La than static. The only explanations for this phenomenon are quick changes in the oxygen metabolism or an enzymatic storage of oxygen. For both gassing out and saturation period it is possible to calculate the same absolute amounts of this additional oxygen.     

The growth and energy metabolism of <Emphasis Type="Italic">Lymnaea stagnalis</Emphasis> (Lymnaeidae,Gastropoda): I. Early postlarval period

The growth and the oxygen consumption rate of Lymnaea stagnalis were studied during the first ten weeks after hatching. It is shown that these processes are atypical during early ontogenesis in comparison with adult mollusks. The obtained data on linear (height of shell) and weight growth can be equally well approximated with the von Bertalanffy equation or exponential and power equations. Both linear and weight growth are characterized by an approximately constant specific rate associated with synchronous oscillations of a week period. The oscillations were observed also for the oxygen consumption rate, but of another period (about 2.6 weeks). On average the metabolic rate after the initial triple increase during the first three days remains stable. The power coefficient of the allometric dependence of the total weight on the shell height is significantly less than that of the adult.     

Cardiac development in crayfish: ontogeny of cardiac physiology and aerobic metabolism in the red swamp crayfish Procambarus Clarkii

The cardiovascular system performs key physiological functions even as it develops and grows. The ontogeny of cardiac physiology was studied throughout embryonic and larval development in the red swamp crayfish Procambarus clarkii using videomicroscopic dimensional analysis. The heart begins to contract by day 13 of development (at 25°C, 20 kPa O₂). Prior to eclosion, heart rate (ƒH) decreases significantly. Previous data suggests that the decrease in cardiac parameters prior to hatching may be due to an oxygen limitation of the embryo. Throughout development, metabolizing mass and embryonic oxygen consumption primarily increased while egg surface area remains constant. The limited area for gas exchange of the egg membrane, in combination with the increasing oxygen demand of the embryo could result in an inadequate diffusive supply of oxygen to developing tissues. To determine if the decrease in cardiac function was the result of an internal hypoxia experienced during late embryonic development, early and late stage embryos were exposed to hyperoxic water (PO₂ =40 kPa O₂). The ƒH in late stage embryos increased significantly over control values when exposed to hyperoxic water suggesting that the suppression in cardiac function observed in late stage embryos is likely due to a limited oxygen supply.     

Ontogenetic change in the relationship between metabolic rate and body mass in a sea bream Pagrus major (Temminck & Schlegel)

Ontogenetic changes in the relationship between resting rate of oxygen consumption and wet body mass were examined at 20° C with the sea bream Pagrus major ranging from 0.00020 g (weight just after hatching) to 270 g (weight at 530 days old). There was a triphasic relationship between oxygen consumption of an individual fish M (μl min⁻¹) and body mass W (g). During a very early stage (weight 0.00020–0.00025 g), corresponding to the pre-larval stage and with the transitional period to the post-larval stage, there was no substantial change in body mass. The mass–specific metabolic rate M/W (μl g⁻¹ min ¹) showed no clear relationship to body mass as expressed by the equation M/ W =4.86 + 1.47 D , where D is age in days. During the post-larval stage (weight 0.00031–0.005 g), M/W remained almost constant independent of body mass following the expression M = 12.5 W0 .949. During the juvenile and later stages (weight 0.005–270 g), M/ W decreased with increasing body mass following the expression M = 6.3 W ^0.821 which is significantly different from the expression for the post-larval stage ( P < 0.001). Ontogenetic changes in the metabolism-body mass relationship are discussed from the viewpoint of relative growth of organs with different metabolic activities.     

Equations describing changes in weight and mass-specific rate of oxygen consumption in animals during postembryonic development

Equations describing growth and respiration rate of animals during postembryonic development have been derived on the basis of thermodynamics of linear irreversible processes. The conditions for equation application are specified as well as the conditions when growth equation can be reduced to the von Bertalanffy equation and when the relationship between the mass-specific rate of oxygen consumption and body weight becomes an allometric relationship.     

Seasonality of torpor and thermoregulation in three dasyurid marsupials

Summary Seasonal variation in the pattern of torpor and temperature regulation was investigated in the closely related arid zone dasyurid marsupialsSminthopsis crassicaudata (17 g),S. macroura (24 g), andDasyuroides byrnei (120 g). The tendency to enter torpor was greater, torpor commenced earlier, torpor duration was longer, and body temperatures (T _b) were lower inSminthopsis spp. than inD. byrnei. The minimum mass-specific rate of oxygen consumption ( ) of torpid animals was similar among the three species despite the differences in minimumT _b. The mass-specific oxygen consumption of normothermic animals was reduced during winter when compared with the summer values in all species, but there was no seasonal variation in normothermicT _b in any species. The tendency to enter torpor was incrased during winter. TorpidSminthopsis spp. had lower values ofT _b and during winter than during summer;D. byrnei did not show seasonal changes in these variables. These results suggest that seasonal changes in the pattern of thermoregulation and torpor in small dasyurids may be more distinct than in larger species.Abbreviations RMR resting metabolic rate - BMR basal metabolic rate     

Assessing maternal effects on metabolic rate dynamics along early development in brown trout (Salmo trutta): an individual-based approach

Routine metabolic rate (oxygen consumption) of individual eggs and larvae of brown trout (Salmo trutta) originating from different families were monitored from fertilisation to the onset of emergence by means of flow through micro-respirometry. This measuring system revealed an accurate tool to measure oxygen consumption on small organisms at the individual level, and daily consumption proved to be very stable. The mass-specific metabolic rate remained low from fertilisation to hatching, and then increased quickly until the age of emergence. A Bayesian modelling approach was used to adequately infer maternal effects on metabolic rate dynamics all along the development period. Substantial differences were found between families, affecting average metabolic rate as well as intra-family variance. That is, offspring originating from different females may have different energetic needs at emergence from gravel. Moreover, between siblings, variability in metabolic rate is also under the influence of maternal effects. Implications of this metabolic rate variability are discussed with regard to life history strategies and early behaviours.