The effects of temperature on the respiration and production of the freshwater nematode Anonchus sp.

Summary Growth and respiration were measured in a species of Anonchus (Nematoda: Plectidae) at 5°C, 10°C, 15°C, 20°C and 25°C. At 5°C no growth was measurable but the organisms remained active. Maximum production occurred at 15°C, but the highest rate of growth occurred at 20°C. Thus, adult size attained is dependent on the temperature of growth. Respiratory energy losses derived from Cartesian diver microrespirometry, increased with temperature up to 25°C. Regression coefficients (b values) derived from a log log linear regression of weight against oxygen consumption varied between 0.574–1.793, the lowest value being attained at 5°C, the highest at 20°C. Based on Q₁₀, production and respiratory energy losses the optimum temperatures for Anonchus appears to lie between 10°C–15°C.     

Effects of some extrinsic factors on the respiratory metabolism of the freshwater leech,poecilobdella viridis (blanchard): desiccation and temperature

The influence of desiccation and temperature on the respiratory metabolism of P. viridis have been investigated. There was a significant (p < 0.05) downfall in the respiratory rates as the period of desiccation increased, but for after 18 hours where it was enhanced significantly. The respiration augmented significantly (p < 0.03) when the temperature of the medium increased. Q₁₀ was significantly high at 32–28°C and was low between 35 and 32°C and 20–10°C Functional significance of these changes to the leeches in combating environmental hazards is briefly discussed.     

Temperature and irradiance and the total daily photosynthetic production of the crown of a Pinus radiata tree

Summary Carbon dioxide exchange rates were recorded for different ages and positions of foliage and parts of the main stem of a 7-m tall Pinus radiata D. Don tree growing in a large, artificially lit, controlled-environment room. Irradiance levels were varied from dark to approximately full sunlight, and air temperatures from 10° to 35°C in 5°C steps. Leaf temperatures within the cuvettes used for CO₂ exchange measurements, however, were up to 5°C higher than the room air temperature set but this varied with position in the tree crown, the shaded lower crown being at approximately room temperature. A balance sheet was prepared to show the photosynthetic gains and respiratory losses of different parts of the crown over 24 h at each air temperature and at irradiances of 400, 270, and 135 W m^-2 during the 8-h photosynthetic period. The greatest daily photosynthetic gain was at 10° C, although this temperature is considered sub-optimal for growth. At temperatures greater than 25° C, even at the greatest irradiance level for 8 h, total respiration was greater than photosynthesis.     

Growth of two Pisidium (Bivalvia,Sphaeriidae) species in the laboratory

Summary Growth of Pisidium casertanum and P. subtruncatum from the profundal of the eutrophic Lake Esrom was followed at four temperatures in the laboratory. The growth rate of both species increased with increasing temperature, but the maximum in P. casertanum was attained at 12° C, instead of at 20° C as in P. subtruncatum. The variation of Q₁₀ of growth in relation to animal weight was of similar form in both species at higher temperatures (6–12°C) but opposite at low temperatures (2–6°C). In the latter case Q₁₀ of P. casertanum had a peak and that of P. subtruncatum a low value at a corresponding size preceding maturity. At constant temperatures growth curves of the form y=a+bx+cx² were obtained, where y is weight in g and x is time in days. The growth of both species under natural conditions was simulated by use of the experimental growth rate equation and natural birth periods, sizes at birth, and temperature cycles. These simulations gave a maximum life span of 2.5–3 years for P. casertanum and 3.5–4.5 years for P. subtruncatum. The latter species showed slower growth rates at the low or medium temperatures prevailing in the profundal of this lake. A comparison with growth in nature reveals that the simulation overestimated growth in case of P. casertanum.     

Dependence of temperature on loss rates of rotifers,lipids, and ω3 fatty acids in starved Brachionus plicatilis cultures

Rotifer cultures of Brachionus plicatilis (SINTEF-strain, length 250 m) rich in 3 fatty acids were starved for > 5 days at variable temperature (0–18 °C). The net specific loss rate of rotifer numbers were 0.04 day^–1 (range 0–0.08 day^–1) at 5–18 °C, but reached values up to 0.25 day^–1 at 0–3 °C. The loss rate was independent on culture density (range 40–1000 ind ml^–1), but was to some extent dependent on the initial physiological state of the rotifers (i.e., egg ratio).The loss rate of lipids was 0.02–0.05 day^–1 below 10 °C, where the potential growth rate of the rotifer is low (0–0.09 day^–1). The loss rate of lipids increased rapidly for higher temperatures where the rotifer can maintain positive growth, and reached 0.19 day^–1 at 18 °C. The Q₁₀ for the lipid loss rate versus temperature was higher than the Q₁₀ for respiration found in other strains. This may suggest that other processes than respiration were involved in lipid catabolism. The content of 3 fatty acids became reduced somewhat faster than the lipids (i.e. in particular 22:6 3), but the fatty acid per cent distribution remained remarkably unaffected by the temperature during starvation.The results showed that rotifer cultures could be starved for up to 4 days at 5–8 °C without essential quantitative losses of lipids, 3 fatty acids, and rotifers. The rotifers exhausted their endogenous lipids through reproduction (anabolism) and respiration (including enhanced locomotion) at higher temperatures. At lower temperatures, the mortality rate became very high.     

Thermal Acclimation of Respiration and Photosynthesis in the Marine Macroalga Gracilaria lemaneiformis (Gracilariales,Rhodophyta)

The responses of respiration and photosynthesis to temperature fluctuations in marine macroalgae have the potential to significantly affect coastal carbon fluxes and sequestration. In this study, the marine red macroalga Gracilaria lemaneiformis was cultured at three different temperatures (12, 19, and 26°C) and at high‐ and low‐nitrogen (N) availability, to investigate the acclimation potential of respiration and photosynthesis to temperature change. Measurements of respiratory and photosynthetic rates were made at five temperatures (7°C–33°C). An instantaneous change in temperature resulted in a change in the rates of respiration and photosynthesis, and the temperature sensitivities (i.e., the Q₁₀ value) for both the metabolic processes were lower in 26°C‐grown algae than 12°C‐ or 19°C‐grown algae. Both respiration and photosynthesis acclimated to long‐term changes in temperature, irrespective of the N availability under which the algae were grown; respiration displayed strong acclimation, whereas photosynthesis only exhibited a partial acclimation response to changing growth temperatures. The ratio of respiration to gross photosynthesis was higher in 12°C‐grown algae, but displayed little difference between the algae grown at 19°C and 26°C. We propose that it is unlikely that respiration in G. lemaneiformis would increase significantly with global warming, although photosynthesis would increase at moderately elevated temperatures.     

Respiration of juvenile Arctic cod (Boreogadus saida): effects of acclimation,temperature, and food intake

Oxygen consumption (VO₂) of juvenile Arctic cod (Boreogadus saida) was investigated at low tempera tures (six temperatures; range -0.5 to 2.7°C). Small (mean wt. 6–8 g) and large (mean wt. 14 g) fish were acclimated, or adjusted to a constant temperature (0.4°C), for 5 months and then tested for metabolic cold adaptation (elevated metabolic rates in polar fishes). Short-term (2 weeks) acclimated fish showed elevated VO₂ similar to previously established values for polar fishes, but there was no such evidence after longterm acclimation. Long-term acclimation caused VO₂ values to drop significantly (from 86.0 to 46.5 mg O₂·kg^–1·h^–1, at 0.4°C), which showed that metabolic cold adaptation was a phenomenon caused by insufficien: acclimation time for fish in respiration experiments. We also measured the effects of temperature and feeding on VO₂. A temperature increase of 2.3°C resulted in relatively large increases in VO₂ for both longand short-term acclimated fish (Q₁₀ = 6.7 and 7.1, respectively), which suggests that metabolic processes are strongly influenced by temperature when it is close to zero. Feeding individuals to satiation caused significant increases in VO₂ above pre-fed values (34–60% within 1–2 days after feeding). Respiration budgets of starved and fed Arctic cod at ambient temperatures in Resolute Bay N.W.T., Canada, were used to model annual respiration costs and potential weight loss. Low respiration costs for Arctic cod at ambient temperatures result in high growth efficiency during periods of feeding and low weight loss during periods of starvation.     

Phytoplankton primary production in a eutrophic cooling water pond

The seasonal variation of phytoplankton photosynthesis was measured with ¹⁴C-method in a warmed ice-free pond in central Finland. Simultaneously with in situ measurements the photosynthesis was also measured in an incubator with different water temperatures and constant light (ca. 16 W m^–2). The total annual photosynthesis was 57.2 C m^–2 a^–1. The portion of the winter and spring production of the annual photosynthesis was 18.4%, that of the autumn production ws 17.4%. Thus 64.3% of the total annual phytoplankton photosynthesis occurred in the three summer months. The range of the daily integrated photosynthesis per unit area was 1.9—563 mg C m^–2d^–1. The photosynthetic rate per unit chlorophyll a varied in situ from 0.94 to 33.1 mg C (mg chl. a)^–1 d^–1. The highest value was measured in the beginning of July and the lowest in mid-January. The photosynthetic rate increased in situ exponentially with increasing water temperature. In the incubator the highest photosynthetic rate values were also found in July and August (at+20 °C) when the phytoplankton population was increasing and the minimum values occurred after every diatom maximum both in spring and autumn. Light was a limiting factor for photosynthesis from September to Mid-January, low water temperature was a limiting factor from late January through May. The efficiency of the photosynthesis varied between 0.1 and 0.7% of P.A.R. According to the incubator experiments the Q₁₀ values for the photosynthesis were 2.45 and 2.44 for the winter population between 1 and 10° C and for the summer population between 5 and 15° C, respectively, but the Q₁₀ values decrease at the higher temperatures. The main effect of the warm effluents on the yearly photosynthesis was the increase of production in spring months due to the lack of ice cover. However, the increase of total annual phytoplankton photosynthesis was only ca. 10–15%, because the water temperature was during the spring months below 10° C.     

Temperature aspects of ecological bioenergetics in Brachionas angularis (Rotatoria)

The influence of temperature and food quality was studied on the following energy balance parameters of B. angularis: ingestion, production, growth and mortality. The ingestion rate rises to an optimum at 15 and 20 °C and decreases at 25 °C. The other rates increase continuously over the 5–25 °C range. The Q₁₀-values of production rate are higher than those of ingestion rate. Temperature also modifies the relationship between food concentration and bioenergetic rates. They react according to a Monod function (production at all temperatures, growth at 10 °C) or decrease at high concentrations (growth at 15° and 20 °C.)     

Energy consumption and metabolism during starvation in the Arctic hyperiid amphipod Themisto libellula Mandt

When the Arctic hyperiid amphipod Themisto libellula was starved for a month the lipid and energy content decreased. Over the first two weeks 5.50 g lipid and 0.24 joules were consumed per mg dry weight·d, but rates of lipid and energy consumption decreased by 70–75% during the subsequent two weeks. An individual with maximum lipid reserve could survive for about 168 days without food. Given that lipid is also needed for reproduction in mid-winter, it seems unlikely that animals could overwinter without feeding. Temperatures between 0° and 6° C had only a slight effect (Q₁₀ = 1.61) on the rate of lipid and energy consumption. The effect of temperatures in the normal habitat range on the rate of respiratory metabolism was also small (Q₁₀ = 2.01), but above 5°C the rate increased sharply (Q₁₀ = 6.5). Starvation for 15 days had no significant effect on the animals' metabolic rate.     

Acclimation of snow gum (Eucalyptus pauciflora) leaf respiration to seasonal and diurnal variations in temperature: the importance of changes in the capacity and temperature sensitivity of respiration

We investigated the relationship between daily and seasonal temperature variation and dark respiratory CO₂ release by leaves of snow gum (Eucalyptus pauciflora Sieb. ex Spreng) that were grown in their natural habitat or under controlled‐environment conditions. The open grassland field site in SE Australia was characterized by large seasonal and diurnal changes in air temperature. On each measurement day, leaf respiration rates in darkness were measured in situ at 2–3 h intervals over a 24 h period, with measurements being conducted at the ambient leaf temperature. The rate of respiration at a set measuring temperature (i.e. apparent ‘respiratory capacity’) was greater in seedlings grown under low average daily temperatures (i.e. acclimation occurred), both in the field and under controlled‐environment conditions. The sensitivity of leaf respiration to diurnal changes in temperature (i.e. the Q₁₀ of leaf respiration) exhibited little seasonal variation over much of the year. However, Q₁₀ values were significantly greater on cold winter days (i.e. when daily average and minimum air temperatures were below 6° and –1 °C, respectively). These differences in Q₁₀ values were not due to bias arizing from the contrasting daily temperature amplitudes in winter and summer, as the Q₁₀ of leaf respiration was constant over a wide temperature range in short‐term experiments. Due to the higher Q₁₀ values in winter, there was less difference between winter and summer leaf respiration rates measured at 5 °C than at 25 °C. The net result of these changes was that there was relatively little difference in total daily leaf respiratory CO₂ release per unit leaf dry mass in winter and summer. Under controlled‐environment conditions, acclimation of respiration to growth temperature occurred in as little as 1–3 d. Acclimation was associated with a change in the concentration of soluble sugars under controlled conditions, but not in the field. Our data suggest that acclimation in the field may be associated with the onset of cold‐induced photo‐inhibition. We conclude that cold‐acclimation of dark respiration in snow gum leaves is characterized by changes in both the temperature sensitivity and apparent ‘capacity’ of the respiratory apparatus, and that such changes will have an important impact on the carbon economy of snow gum plants.     

Light-temperature interactions in the control of photosynthesis in Antarctic phytoplankton

Summary During October/November 1983 photosynthetic responses of natural phytoplankton from the Scotia Sea and Bransfield strait to light and temperature were examined in incubators. Both assimilation numbers at saturating light levels and the slopes of the light-limited portions of the photosynthesis versus irradiance curves were smaller than in algae from lower latitudes. However, both parameters increased significantly with rising temperatures. Light-saturated photosynthesis on the average exhibited a Q₁₀-value of ca. 4.2 between-1.5°C and +2°C. Light-limited photosynthesis between-1.5°C and +5°C rose at a rate corresponding to a Q₁₀-value of roughly 2.6. Above +5°C, temperature enhancement of both light-saturated and light-limited photosynthetic rates was minimal or absent. Our results suggest that under extremely low temperatures light-limited photosynthetic rates become temperature-dependent due to changes in maximum quantum yields.     

Long-Term Effects of Elevated CO2 on Woody Tissues Respiration of Norway Spruce Studied in Open-Top Chambers

In an open-top chamber experiment located in a mountain stand of 14-years-old Norway spruce (Picea abies [L.] Karst.), trees were continuously exposed to either ambient CO₂ concentration (A), or ambient + 350 µmol mol^–1 (E) over four growing seasons. Respiration rates of different woody parts (stem, branches, coarse roots) were measured during the last growing season. The calculated increase in the respiration rate related to a 10 °C temperature change (Q₁₀) was different in stem compared to branches and roots. Differences between the E and A variants were statistically significant only for roots in the autumn. Stem maintenance respiration (R_Ms) measured in April and November (periods of no growth activity) were not different. The stem respiration values (R_s) were recalculated to a standard temperature of 15 °C to estimate the seasonal course. The obtained R_s differed significantly between used variants during July and August. At the end of the season, R_s in E decreased slower than in A, indicating some prolongation of the physiological activity under the elevated CO₂ concentration. The total stem respiration carbon losses for the investigated growing season (May – September) were higher for A (2.32 kg(C) m^–2 season^–1) compared to E (2.12 kg(C) m^–2 season^–1). The respiration rates of the whorl branches (R_b) were lower compared with the stem respiration but not significantly different between the used variants. The root respiration rate was increased in E variant.     

Habitat temperature and potential locomotor activity of the continental Antarctic mite,Maudheimia petronia Wallwork (Acari: Oribatei)

Microhabitat recordings suggest that the continental Antarctic mite Maudheimia petronia Wall-work experiences temperatures above 0°C for 60% of the time during summer (about 2 months). Summer daily maximum temperatures are, however, often relatively high (the highest recorded temperature was 27.7°C). Because the locomotor activity of this mite is suppressed at freezing temperatures, the time available for activity, and probably also feeding, is restricted. Temperature relations of potential locomotor activity rate suggest alleviation of this time constraint through the maximization of the rate. The locomotor activity rate of M. petronia is positively sensitive to the entire range of above-zero temperatures that it naturally experiences, being particularly accelerated at lower temperatures (Q_100°–5°C values were above 13, whereas Q_{1025°–30°C} values were below 2). Also, comparisons between mites acclimated at -15°C and 10°C suggest an inverse temperature acclimation of this rate. We hypothesize that potential feeding rate is similarly related to temperature. A relative enhancement of food intake would seem important, not only for the maintenance of a daily positive energy balance in summer, but also for the building up of energy reserves for the relatively long winter, when feeding is impossible.     

Oxygen consumption and ammonia excretion of herbivorous chironomid larvae in Lake Balaton

The oxygen consumption and ammonia excretion of a herbivorous midge larva,Chironomus sp., inhabiting Lake Balaton was measured at two different temperatures. The loss of energy through respiration and that through ammonia excretion were calculated. The daily respiratory energy loss amounted to 655.5 ± 123.8 J g^–1 at 17 °C and to 1 160.0 ± 168.4 J g^–1 (dry weight) at 25 °C. Mean energy loss through ammonia excretion was about 40% less than through respiration.     

Respiratory energy losses related to cell weight and temperature in ciliated protozoa

Summary Respiratory energy losses in five species of ciliated protozoa, Tetrahymena pyriformis Ehrenberg, Vorticella microstoma Ehrenberg, Paramecium aurelia Ehrenberg, Spirostomum teres Claparède and Lachmann and Frontonia leucas Ehrenberg, were investigated at 8.5° C, 15° C and 20° C using Cartesian diver microrespirometry. Q ₁₀ values of 1.15–2.24 were found for four of the species between 8.5–15° C, while in S. teres a Q ₁₀ of 12.98 occurred between these temperatures. Between 15–20° C T. pyriformis and P. aurelia had Q ₁₀ values of 3.73 and 1.56, respectively. Linear double log regressions of oxygen consumption vs. dry weight were derived at each temperature and regression coefficients (b) of 0.2723 (8.5° C), 0.4364 (15° C) and 0.4171 (20° C) were obtained. The results are explained and discussed in relation to previous work on the energetics of ciliated protozoa.     

Influence of temperature and ambient oxygen on the swimming energetics of cyprinid larvae and juveniles

Synopsis The relationship between respiration and swimming speed of larvae and juveniles (2–100 mg fresh mass) of Danube bleak, Chalcalburnus chalcoides (Cyprinidae), was measured at 15° and 20° C under hypoxic (50% air saturation), normoxic, and hyperoxic (140% air saturation) conditions. In a flow-tunnel equipped with a flow-through respirometer the animals swam at speeds of up to 8 lengths · s^-1; speeds were sustained for at least two minutes. The mass specific standard, routine, and active respiration rates declined with increasing body mass at both temperatures. Metabolic intensity increased with temperature, but also the critical swimming speed (at which oxygen uptake reached its maximum) was higher at 20° than at 15° C by about 30%. Nevertheless, the oxygen debt incurred by the fish at the highest speeds was about 40%, and the net cost of swimming about 32%, lower at 20° than at 15°C. The standard metabolic rate was more strongly dependent on temperature (Q₁₀ around 2.5) than the maximum active rate (Q₁₀ below 2). Whereas standard and routine respiration rates were well regulated over the pO₂-range investigated (8.5–25.8 kPa), the active rates showed a conformer-like pattern, resulting in factorial scopes for activity between 2 and 4. Under hypoxia, the critical swimming speed was lower than under normoxia by about 1.51 · s^-1, but the net cost of swimming was also lower by about 30%. On the other hand, hyperoxia neither increased the swimming performance nor did it lead to a further increase of the metabolic cost of swimming. The hypoxia experiments suggest that in response to lowered tensions of ambient oxygen maintenance functions of metabolism not directly related to swimming may be temporarily reduced, leading to increased apparent swimming efficiency under these conditions. The responses of the larvae of Danube bleak to low temperature and low ambient oxygen are discussed in terms of the metabolic strategies by which energy-limited animals meet the challenge of environmental deterioration.     

Compared thermoluminescence characteristics of pea thylakoids studied in vitro and in situ (in leaves). The effect of photoinhibitory treatments

Characteristics of thermoluminescence (TL) glow curves were studied in thylakoids (isolated from pea leaves) or in intact pea leaves after an exposure to very high light for 2 min in the TL device. The inhibition of photosynthesis was detected as decreases of oxygen evolution rates and/or of variable fluorescence.In thylakoids exposed to high light, then dark adapted for 5 min, a flash regime induced TL glow curves which can be interpreted as corresponding to special B bands since: 1) they can be fitted by a single B band (leaving a residual band at –5°C) with a lower activation energy and a shift of the peak maximum by –5 to –6°C and, 2) the pattern of oscillation of their amplitudes was normal with a period of 4 and maxima on flashes 2 and 6. During a 1 h dark adaptation, no recovery of PS II activity occurred but the shift of the peak maximum was decreased to –1 to –2°C, while the activation energy of B bands increased. It is supposed that centers which remained active after the photoinhibitory treatment were subjected to reversible and probably conformational changes.Conversely, in intact leaves exposed to high light and kept only some minutes in the dark, TL bands induced by a flash regime were composite and could be deconvoluted into a special B band peaking near 30°C and a complex band with maximum at 2–5°C. In the case of charging bands by one flash, this low temperature band was largely decreased in size after a 10 min dark adaptation period; parallely, an increase of the B band type component appeared. Whatever was the flash number, bands at 2–5°C were suppressed by a short far red illumination given during the dark adaptation period and only remained a main band a 20°C; therefore, the origin of the low temperature band was tentatively ascribed to recombinations in centers blocked in state S₂Q_A ^–Q_B ^2–. In vivo, the recovery of a moderately reduced state in the PQ pool, after an illumination, would be slow and under the dependence of a poising mechanism, probably involving an electron transfer between cytosol and chloroplasts or the so-called chlororespiration process.Abbreviations E_a- activation energy - FR- far-red - MV- methylviologen - pBQ- p-benzoquinone - PQ- plastoquinone - PS II- Photosystem II - Q_A- primary quinone electron acceptor of PS II - Q_B- secondary quinone electron acceptor of PS II - TL- thermoluminescence     

Respiratory metabolism of mosquitofish,Gambusia affinis: effects of temperature,dissolved oxygen,and sex difference

Synopsis Routine respiratory metabolic rates of mosquitofish (0.2 g live weight) were determined at 10, 15, 20, 25, 30, and 35°C at normoxic, hypoxic (= 40 torr P_O2), and extreme hypoxic (= 25 torr P_O2) conditions. Rates generally increased with increases in temperature (overall Q₁₀ = 2.11 at normoxia). Significant depressions (P<0.05) in rates were measured at 30 and 35°C at extreme hypoxic conditions. Males exhibited higher mortality at extreme hypoxia than females, especially at 35°C. Metabolic rates were significantly elevated at hyperoxic conditions (= 300 torr P_O2) at 25 and 30°C, but not at 35°C. Resting routine rates of less-confined fish were determined at 20, 25, and 30°C at normoxia and were significantly lower than the routine rates at the same temperatures. Behavioral experiments showed that aquatic surface respiration is initiated by mosquitofish at 20–65 torr P_O2 and is obligatory below 20 torr at 20° C. Overall, respiratory metabolic rates provide a quantitative metabolic basis from which predation rates of mosquitofish in various environments can be estimated.