Otolith oxygen and carbon stable isotopes in wild and laboratory-reared plaice (Pleuronectes platessa)

The relationship between water temperature, growth rate, and otolith isotopic ratios was measured for juvenile plaice (Pleuronectes platessa) reared at two temperatures (11 and 17°C) and two feeding regimes (1 and 3 prey items·ml^?1). The otolith isotope ratios in individual fish ranged from ?2 to ?4 for carbon isotope ratios (δ¹³C) and from 0.2 to 1.9 for oxygen isotope ratios (δ¹⁸O). The otolith oxygen isotope ratios were significantly affected by water temperature, but not by feeding level, and there were no significant synergistic effects. The fractionation of oxygen isotopes during otolith growth was independent of individual growth rate. Carbon isotope ratios were not significantly affected by food ration or water temperature, but were related to fish growth rate. The carbon isotope ratios were negatively correlated with fish length in the colder water treatments, and tended to increase with fish length in the warm water treatments. The laboratory-determined relationship between otolith oxygen isotope ratio and water temperature was applied to individuals of five species (plaice, cod, whiting, haddock, gurnard) collected in a single trawl sample. The otolith derived temperatures often overestimated measured water temperatures. The difference between real and estimated water temperatures varied between species, and the closest fit was for field-caught plaice.     

An experimental study of the oxygen consumption,growth, and metabolism of the COD (Gadus Morhua L.)

The rate of oxygen consumption of cod in sea water at 12 °C containing MS222 (25 mg/l) can be expressed as: Q_o2 = 0.245 W^0,82(mg/h), where W is the lived weight of the fish (g). The maximum efficiency of conversion of assimilated food into growth was 24% during the feeding experiment. Digestion efficiencies were estimated at over 98% using fillets of plaice as food. The effect of increasing the rate of food intake was to increase liver weight and condition factor. The relative proportions of protein and lipid in the body did not change over the range of feeding levels used. The conversion efficiency had a maximum value at an intermediate feeding rate.     

Influence of oxygen and temperature on growth and metabolic performance of Paralichthys lethostigma (Pleuronectiformes: Paralichthyidae)

In this study, we apply Fry's classification of environmental factors to demonstrate the limiting effects of oxygen and its interaction with temperature on the growth of juvenile P. lethostigma. We also evaluated the properties of two metabolic indices, marginal metabolic scope (MMS) and limiting oxygen concentration (LOC), as indicators of metabolic scope. We found that oxygen limitation has its greatest impact near the optimum temperature for growth of the species. At 29 °C a reduction from 6.00 mg/L to 4.00 mg/L caused a 50% reduction in growth rate while at 27 °C the reduction had no significant effect on growth rate. The results are particularly relevant because these temperatures and oxygen concentrations are commonly observed in nursery areas during summer months. At all temperatures fish from the lowest oxygen treatment (1.75 mg/L) had negative growth rates. Comparisons between daily oscillating oxygen treatments and constant treatments failed to demonstrate significant effects. At temperatures past the optimum, growth rates between the 6.00 mg/L and 4.00 mg/L treatments were not statistically different. LOC was significantly affected by temperature, oxygen, and their interaction. Estimates were positively correlated with oxygen treatment (R² > 0.71) and negatively correlated with temperature at moderate and low oxygen concentrations (R² > − 0.84). MMS was significantly affected by temperature and oxygen and was significantly correlated with oxygen treatment (R² > − 0.91), but correlations with temperature were not as clear. In conclusion, oxygen and temperature interactions have significant effects on metabolic scope and growth rates of fish, well above the accepted hypoxia threshold of 2.00 mg/L and MMS has proved a useful estimator of the metabolic scope of the organism within an environment.     

Effects of irradiance on relative growth rates, net assimilation rates, and leaf area partitioning in cotton and three associated weeds

Cotton (Gossypium hirsutum L. var. `Stoneville 213'), velvetleaf (Abutilon theophrasti Medic.), redroot pigweed (Amaranthus retroflexus L.), and hemp sesbania (Sesbania exaltata [Raf.] Cory) were grown in a controlled environment room at 31/25 C day/night temperature and three irradiances: 90, 320, and 750 μeinsteins meter⁻² second⁻¹. From total dry weights and leaf areas determined at intervals during the first exponential phase of growth, we used mathematical growth analysis techniques to calculate net assimilation rates (NAR), relative growth rates (R_w), relative leaf area expansion rates (R_a), leaf area partition coefficients (LAP), and leaf area ratios (LAR). In all four species, R_w, R_a, and NAR decreased with decreasing growth irradiance, while LAP and LAR increased. Within each species, R_w was positively correlated with NAR but negatively correlated with LAP and LAR. In comparisons among the four species within each growth irradiance, R_w was positively correlated with LAP. We discuss the relationship between LAP and LAR and show that LAP = (R_a/R_w) (LAR).     

Advantages of NH4 + on growth, nitrogen uptake and root respiration of Phragmites australis

We investigated growth, N nutrition, and root respiration in Phragmites australis (Cav.) Trin. ex Steud. grown under conditions with different N sources, and evaluated the advantages of NH₄ ⁺ nutrition in relation to adaptation to anaerobic soil conditions. Hydroponics culture was carried out for 2 months under two treatment conditions with different N sources, NH₄ ⁺ and NO₃ ^?. The relative growth rate (RGR) of the roots, shoot and whole plant, net N uptake rate (NNUR), and root respiration rate were examined. Shoot RGR, shoot to root (S/R) ratio, and NNUR were obviously higher with the NH₄ ⁺ treatment. High S/R ratio of plants grown in the NH₄ ⁺ treatment contributed to repression of whole-root oxygen consumption. In consequence, NNUR per root respiration rate was higher with the NH₄ ⁺ treatment, which clearly suggested efficient oxygen consumption in the roots. In conclusion, higher S/R ratio due to higher NNUR enable to efficiently use oxygen for N nutrition through the repression of whole-root oxygen consumption, which is consequently achieved by NH₄ ⁺ nutrition. Therefore, we suggest that NH₄ ⁺ nutrition is indispensable for hydrophytic species growing in anaerobic soil because it enables both sufficient N nutrition and efficient oxygen consumption.     

Ecosystem respiration and its controlling factors in a coniferous and broad-leaved mixed forest in Dinghushan, China

Accurate estimation of ecosystem respiration (R_eco) in forest ecosysteM_s is critical for validating terrestrial carbon models. Continuous eddy covariance measuremenT_s of R_eco were conducted in a coniferous and broad-leaved mixed forest located in Dinghushan Nature Reserve of southern China. R_eco was estimated and the controlling environmental factors were analyzed based on two years' data from 2003 to 2004. Major resulT_s included that: (1) R_eco was affected by soil temperature, soil moisture, canopy air temperature and humidity, where soil temperature at 5 cm depth was the dominant factor. (2) The exponential equation, Van't Hoff equation, Arrhenius equation and Lyold-Talor equation can be used to describe the relationship between R_eco and temperature factors with similar statistical significance, while Lyold-Talor equation was the most sensitive to the temperature index (Q₁₀). (3) The multiplicative model driven by soil temperature (T_s) and soil moisture (M_s) was more corresponsive to R_eco, which explained that there were more R_eco variations than Lyold-Talor equation, both for higher and lower M_s. However, there was no statistical difference between the two models. (4) Annually accumulated R_eco of the mixed forest in 2003 was estimated as 1100–1135.6 gC m^?2 a^?1 by using daytime data, which was 12%–25% higher than R_eco (921–975 gC m^?2 a^?1) estimated by using nighttime data. The resulT_s suggested that using daytime data to estimate R_eco can avoid the common underestimation problem caused by using eddy covariance methods. The study provides a basic method for further study on accurate estimation of net ecosystem CO₂ exchange (NEE) in the coniferous and broad-leaved mixed forest in southern China.     

Partitioning of oxygen consumption between “maintenance” and “growth” in developing herring Clupea harengus (L.) embryos

Growth and oxygen consumption was measured in developing herring Clupea harengus (L.) embryos. By considering the variations in oxygen consumption with embryonic size and growth rate, an attempt was made to partition oxygen consumption between growth related and growth unrelated (i.e., “maintenance”) processes. The metabolic cost of growth was estimated as ≈ 150 ng O₂ · μg dry wt tissue formed⁻¹. This estimate compares favourably with the biochemical estimate of the costs of transport and net biosynthesis. The “maintenance” component was proportional to embryonic mass (77 ng O₂ · μg⁻¹· d⁻¹). Over the entire embryonic period, growth processes were responsible for ≈ 25% of the cumulated oxygen consumption.     

Versuche über die Abhängigkeit der Atmung vonArenicola marina (Annelides Polychaeta) von Größe und Temperatur

A knowledge of the rate of oxygen consumption is very important for the evaluation of many physiological and ecological problems. Among the many factors affecting respiratory rate, water temperature and body size are particularly considered here. The modifying effects of body size may be expressed mathematically by the allometric formula: y=b · w ^a , where b represents the rate of O₂ consumption of an individual whose weight is expressed in a chosen metrical weight unity (i. e. in grams, ounces, etc.), anda represents the decrease of metabolic rate during growth. InArenicola the exponent is not the same at all temperatures tested. In most cases it lies between 0.7 and 0.8, i. e., between a weight proportional respiratory rate and a surface proportional one. Minimum values fora were found in experiments conducted in summer at 20° C and in spring at 15° C. They characterize an optimum efficiency of metabolism at these temperatures. Determinations of b demonstrated that metabolic rate ofArenicola is significantly less affected in spring (10° to 20° C) and autumn (10° to 25° C) than is usually known from biological processes. However, the temperature coefficients above and below these temperature ranges are very high. Another break in the temperature-rate curve could be demonstrated below 5° C in spring.     

Thermal dependence of tissue metabolism in the green turtle,Chelonia mydas

To better understand how tissue specific metabolic rates might contribute to the maintenance of elevated body temperatures in green turtles (Chelonia mydas), we determined the effect of temperature on oxygen consumption of green fat, small intestine, nonswimming skeletal muscle, pectoralis muscle, liver, heart, and kidney tissues from 5–35°C. We found a direct relationship between tissue metabolic rate (microliters of O₂/g wet mass per hour) and temperature in all tissues measured except for green fat. The Q₁₀ values ranged from 0.65 to 3.38. There were significant differences in metabolic rate among tissues as well as in how temperature influenced tissue metabolic rates. Tissue metabolic rates were highest in kidney and heart tissues. Green fat and small intestine had the lowest and most temperature-insensitive values. Muscle tissue had a high oxygen consumption relative to other reptiles, and this elevated metabolism may provide a functional advantage for long distance swimming and heat production.     

Oxygen consumption by the bivalve Donax vittatus (da Costa)

The acute oxygen consumption of Donax vittatus (da Costa) freshly collected at different times from a beach at Barrassie, Ayrshire, Scotland, has been measured at different temperatures. The logarithmic relationship between oxygen consumption and body weight showed a significant difference on only one occasion, and a common regression coefficient (b) of 0.865 could be used for regressions of oxygen consumption on weight. Over the temperature range 2.9–20 °C oxygen consumption rose with temperature. There was a linear decline of Q₁₀ with temperature in the range 2.9 –20 °C. Differences in values of the constant (a) in the regression equation suggest that there is some acclimation to temperature, resulting in rotation of the rate/temperature curve counterclockwise for warm-acclimated animals, and a reduction of Q₁₀ in cold-acclimated animals. The differences in oxygen consumption which result are small and appear to have little practical significance. High levels of metabolically-inactive materials such as stored glycogen reserves lead to a reduction in the weight-specific oxygen consumption. Spawning animals show an increased oxygen consumption.     

Water balance of over-wintering beetles in relation to strategies for cold tolerance

The vapour pressure of the haemolymph of a supercooled insect is higher than the vapour pressure of the haemolymph of a frozen insect at the same temperature. The aim of the study was to see whether this may affect the water loss of freeze-avoiding and freezetolerant, over-wintering beetles. The rates of water loss were determined on freeze-tolerant Pytho depressus larvae and Upis ceramboides adults. Within each species one group was kept supercooled whereas another group was frozen. All groups were incubated at-5°C. Both species displayed significantly lower rates of water loss when they were frozen than when they were supercooled. Values of respiratory rate and water loss of freeze-avoiding and freeze-tolerant species were compared to corresponding values of desert beetles. The results indicate that the freeze-avoiding species have lower rates of cuticular water loss than freeze-tolerant species. This indicates that the freeze-avoiding species have developed more efficient water-saving mechanisms than freeze-tolerant species. The reason for this may be that the haemolymph in frozen animals will be in vapour pressure equlibrium with the ice in the hibernaculum and thus there is no danger of desiccation during winter. The supercooled insects will have a vapour pressure of the haemolymph that is higher than the vapour pressure of water in the surrounding air and will thus lose water.Abbreviations BW body weight - BW_i initial body weight - BW_t body weight at time t - P vapour pressure difference between the water in the haemolymph and the water in the air - DWL_t dry weight loss at time t - M _w rate of metabolic water production - MF_w mol fraction of water, in the haemolymph - MO₂ rate of oxygen consumption - Osm osmolality of the haemolymph - P _a vapour pressure of water in the air - P _h vapour pressure of water in the haemolymph - P _w vapour pressure of pure water - Q a constant (2,02 1 oxygen per g fat metabolized) relating oxygen consumption to dry weight loss when fat is metabolized - R a constant (1,89 1 oxygen per g water produced) relating metabolic water production to oxygen consumption when fat is metabolized - R _dwl rate of dry weight loss - RH relative humidity of the air - RWC_i initial relative water content measured by weighing - RWC_t relative water content at time t - STP standard temperature and pressure     

Rates of oxygen consumption by Thais (Nucella) Lapillus (L.)

Oxygen consumption by Thais varied seasonally with higher values in summer than in winter. This seasonal difference was due in part to the effects of temperature and in part to those of feeding. During feeding, rates of oxygen consumption were high, but declined in the period between meals. There was little evidence of acclimation of oxygen consumption to changes in temperature; low (winter) rates of consumption were more sensitive to increases in temperature than were high (summer) rates. A polynomial expression, including terms for temperature and ‘time since last meal’, was derived for the constant a′ in the allometric equation relating oxygen consumption (_o2) to dry body weight: _o2 = a′.W^0.511.     

Effects of HgCl2 on principal parameters of exudation from maize detached root system

To elucidate the role of aquaporins in the control of the root pressure, we tested the effects of HgCl₂ (aquaporin blocker) at concentrations from 10^?8 to 10^?2 M on the exudation rate (J _w). Experiments were performed with detached roots of 5–7-day-old etiolated maize (Zea mays L.) seedlings. HgCl₂ suppressed exudation by 50–70% at the concentration of 2 × 10^?5 M. At the concentration of 2.5 × 10^?4 M, HgCl₂ reduced J _w during first 20–40 min, but in 2 h, it activated exudation by ten and more times. In this case, the root and osmotic pressures of the exudates increased by 1.5 times. The hydraulic conductance reduced approximately by 30% during first 30 min and increased severalfold in 2 h. The temperature coefficient (Q₁₀) of J _w attained 14 in 2 h. At the concentration of 10^?2 M, HgCl₂-induced acceleration of exudation was replaced by its inhibition essentially immediately. We suggested that a driving force for HgCl₂-induced stimulation of the J _w might be an increase in the osmotic component of the root pressure or the involvement of its nonosmotic (so-called metabolic) component. The results allow a supposition that aquaporins are involved in the control of water transport in the root.     

Optimizing the Continuous Production of Candida utilis and Saccharomycopsis fibuliger on Potato Processing Wastewater

The yeasts Candida utilis and Saccharomycopsis fibuliger were propagated as a source of single-cell protein in a continuous, mixed, aerobic, single-stage cultivation on blancher water generated during potato processing. A series of steady-state experiments based on a two-level factorial design, half-replicate modified with an intermediate experiment, was performed to determine the effect of pH, 3.8 to 4.8; dissolved oxygen, 42 to 80% saturation; dilution rate, 0.17 to 0.31 h⁻¹; and temperature, 27 to 32°C on the amount of carbon consumed, the rate of carbon consumption (R_c), the amount of reducing sugar consumed, the rate of sugar consumption (R_g), the amount of protein produced, the rate of protein production (R_p), the yield from carbon, and the yield from reducing sugar. The results were analyzed by stepwise multiple regression and Fisher's least significant difference test. Analyses showed that high dilution rates resulted in increased R_c, R_g, and R_p and indicated that a rate of 0.31 h⁻¹ was below the critical dilution rate. A temperature of 32°C increased the amount of carbon consumed by 34%. A pH of 4.3 to 4.8 increased the amount of protein produced. The yield from carbon was constant, and the relatively high yield from reducing sugar indicated that other substrates were consumed. Dissolved oxygen was in excess at 42% saturation and above. Since C. utilis predominated the mixed cultures and amylase production appeared to be limited, a single-stage fermentation lacked efficiency. The experimental design allowed preliminary optimization of major environmental variables with relatively few experiments and provided a basis for future kinetic studies.     

Oxygen consumption rate in rotifers

The oxygen consumption rate (OCR) is a cumulative index of metabolic losses during aerobic metabolism. The generalized relationship of oxygen consumption rate (R, n1 O₂ ind^–1 h^–1) and dry body mass (M, µg) for rotifers is described by the equation: R = 9.15M^0.716. The level of rotifer metabolism is slightly lower than that of multicellular poikilothermic animals. Differences of OCR values in ontogenesis are substantial. Embryos and senile individuals are characterized by minimal OCR values. The OCR of oviparous females in the beginning of reproduction exceeds 2–3 times OCR values of juveniles. Differences in oxygen consumption intensity (OCI) are not so essential. OCR depends on food concentration. An increase of food concentration from 1.4 to 7.0 µg dry mass m1^–1 resulted in Brachionus calyciflorus in an OCR escalation of 2.5 times at 30°C, and 0.5 times at 25°C. Maximal OCR values occur at food concentration close to the saturation concentration for population growth rate. An exponential equation is adequate to describe R-t dependence for animals, long-term adapted to different constant temperatures (2 < Q₁₀ < 3). Acclimation effects observed during sharp temperature changes are determined by peculiarities of compensation reactions in species and separate populations. The formation of a zone of relative temperature independence of OCR (Q¹⁰ 1) at fluctuating temperature is observed. It is necessary to study enzymatic activities parallel to OCR and OCI measurements.     

Respiratory metabolism of Alaskozetes antarcticus

Measurements of oxygen consumption in all post-embryonic life stages of U.K. cultured Alaskozetes antarcticus (Acari: Cryptostigmata) showed that log₁₀ respiration rate was linearly related to log₁₀ live weight, while log_e metabolic rate was linearly related to the reciprocal of the absolute temperature over the range 273–283°K, although the magnitude of response to temperature shown by different life stages was found to vary. Differences were apparent between cultured animals and previous measurements made on field animals, especially in respect of the relationship between respiration rate and live weight. The data were found to support the hypothesis of cold adaptation by means of metabolic rate elevation and a possible mechanism in discussed.     

Effect of temperature on the embryonic development of the plaice, Pleuronectes Platessa L. (teleostei)

In normalyears, eggs and prolarvae of the plaice (Pleuronectes platessa L.) in the southern North Sea develop within the temperature range 6.0–8.5 °C, although the water may at times be some degrees colder or warmer than this. The effect of temperature, t °C, on the embryonic development time, D days, has been investigated within the tolerated range 2.8–10.5 °C. Various models to express the observed curvilinear relationship between t and D have been considered, that giving the closest fit to the data being (t−t₀)(D−D₀) = k or $\text{D =}\text{k}\text{(t−t}{}_0\text{)+D}{}_0$. A method is given for the calculation of constants k, D₀, and t₀. The relationship may also be expressed by the equation D = a(t−t₀)^b where a and b are constants, but t₀ must in this case be found by iteration. At investigated temperatures in the range 4.1–10.5 °C the smallest eggs in a batch from a single source hatched first. Within the tolerated range, hatching prolarvae were substantially smaller at 10.5 °C than at the other temperatures. During the period of prolarval yolk utilization, growth is slower at the high temperatures, so that median temperatures of 6.5–8.0 °C are most efficient in terms of the relationship between growth in length and yolk utilization. Toward the end of the yolk-sac phase, the rate of yolk utilization declines unless a suitable external food source (e.g., Artemia nauplii) is provided.     

The combined effect of body size and temperature on oxygen consumption rates and the size-dependency of preferred temperature in European perch Perca fluviatilis

The present study determined the effect of body mass and acclimation temperature (15–28°C) on oxygen consumption rate (ṀO₂) and the size dependency of preferred temperature in European perch Perca fluviatilis. Standard metabolic rate (SMR) scaled allometrically with body mass by an exponent of 0.86, and temperature influenced SMR with a Q₁₀ of 1.9 regardless of size. Maximum metabolic rate (MMR) and aerobic scope (MMR-SMR) scaled allometrically with body mass by exponents of 0.75–0.88. The mass scaling exponents of MMR and aerobic scope changed with temperature and were lowest at the highest temperature. Consequently, the optimal temperature for aerobic scope decreased with increasing body mass. Notably, fish <40 g did not show a decrease aerobic scope with increasing temperature. Factorial aerobic scope (MMR × SMR⁻¹) generally decreased with increasing temperatures, was unaffected by size at the lower temperatures, and scaled negatively with body mass at the highest temperature. Similar to the optimal temperature for aerobic scope, preferred temperature declined with increasing body mass, unaffectedly by acclimation temperature. The present study indicates a limitation in the capacity for oxygen uptake in larger fish at high temperatures. A constraint in oxygen uptake at high temperature may restrict the growth of larger fish with environmental warming, at least if food availability is not limited. Furthermore, behavioural thermoregulation may be contributing to regional changes in the size distribution of fish in the wild caused by global warming as larger individuals will prefer colder water at higher latitudes and at larger depths than smaller conspecifics with increasing environmental temperatures.