Comparative study of dark respiration in plants inhabiting arctic (Wrangel Island) and temperate climate zones

Comparative analysis of dark respiration was carried out for 18 plant species inhabiting arctic zone (Wrangel Island, lat. 71° N) and temperate zone (Leningrad oblast, lat. 59° N). For 15 pairs of species examined, the Stocker’s rule was proved valid; i.e., respiration rates of identical species were equal at average temperatures of their natural habitats. The concept of respiratory features in boreal and mountain plants is described in its historic development. The possible causes for controversial data are explained. It is concluded that gas exchange measurements in natural plant habitats are the only valid means for characterizing plant respiration. Only such measurements should provide the basis for the discussion of global climate changes.     

The relationship between respiration and temperature in leaves of the arctic plant Saxifraga cernua

Abstract Saxifraga cernua, a perennial herb distributed throughout the arctic and subarctic regions, shows high levels of dark respiration. The amount of respiration exhibited by leaves and whole plants at any temperature is influenced by the pretreatment temperature. Plants grown at 10°C typically show higher dark respiration rates than plants grown at 20°C. The levels of alternative-pathway respiration (or cyanide-insensitive respiration) in leaves of S. cernua grown at high and low temperatures were assessed by treating leaf discs with 0.25 mol m^?3 salicylhydroxamic acid during measurements of oxygen consumption. Alternative pathway respiration accounted for up to 75% of the total respiration. Tissues from 20°C-grown plants yielded a Q₁₀ of 3.37 for normal respiration, and of 0.97 for alternative-pathway respiration. Tissues from 10°C-grown plants yielded a Q₁₀ of 2.55 for normal respiration, and of 0.79 for alternative-pathway respiration. The alternative pathway does not appear to be as temperature sensitive as the normal cytochrome pathway. A simple energy model was used to predict the temperature gain expected from these high rates of alternative-pathway respiration. The model shows that less than 0.02°C can be gained by leaves experiencing these high respiration rates.     

THE ECOLOGY OF ARCTIC AND ALPINE PLANTS

‘How are plants adapted to the low temperatures and other stresses of arctic and alpine environments ?’ At present it is not possible to answer this question completely. Much work remains to be done, particularly on low-temperature metabolism, frost resistance, and the environmental cues and requirements for flowering, dormancy, regrowth, and germination. However, in brief, we can say that plants are adapted to these severe environments by employing combinations of the following general characteristics: 1. Life form: perennial herb, prostrate shrub, or lichen. Perennial herbs have greatest part of biomass underground. 2. Seed dormancy: generally controlled by environment; seeds can remain dormant for long periods of time at low temperatures since they require temperatures well above freezing for germination. 3. Seedling establishment: rare and very slow; it is often several years before a seedling is safely established. 4. Chlorophyll content: in both alpine and arctic ecosystems not greatly different on a land-area basis from that in temperate herbaceous communities. Within a single species there is more chlorophyll in leaves of arctic populations than in those of alpine populations. 5. Photosynthesis and respiration: (a) These are at high rates for only a few weeks when temperatures and light are favourable. (b) Optimum photosynthesis rates are at lower temperatures than for ordinary plants; rates are both genetically and environmentally controlled with phenotypic plasticity very marked. (c) Dark respiration is higher at all temperatures than for ordinary plants; rate is both genetically and environmentally controlled, with phenotypic plasticity very pronounced, i.e. low-temperature environment increases the rate at all temperatures. (d) Alpine plants have higher light-saturation values in photosynthesis than do arctic or lowland plants; light saturation closely tied to temperature. (e) There is some evidence that alpine plants can carry on photosynthesis at lower carbon dioxide concentrations than can other plants. (f) Annual productivity is low, but daily productivity during growing season can be as high as that of most temperate herbaceous vegetation. Productivity can be increased by temperature, nutrients, or water. 6. Drought resistance: most drought stress in winter in exposed sites is due to frozen soils and dry winds. It is met by decreased water potentials, higher concentrations of soluble carbohydrates, and closed stomates. Little drought resistance in snowbank plants. Alpine plants adapted to summer drought stress can carry on photosynthesis at low water potentials; alpine or arctic plants of moist sites cannot do this. 7. Breaking of dormancy: controlled by mean temperatures near or above 0° C., and in some cases by photoperiod also. 8. Growth: very rapid even at low positive temperatures. Respiration greatly exceeds photosynthesis in early re-growth of perennials. Internal photosynthesis may occur in hollow stems of larger plants during early growth. Nitrogen and phosphorus often limiting in cold soil. 9. Food storage: characteristic of all alpine and arctic plants except annuals. Carbohydrates mostly stored underground in herbaceous perennials. Lipids in old leaves and stems of prostrate evergreen shrubs. Depleted in early growth, and usually restored after flowering. 10. Winter survival: survival and frost resistance are excellent after hardening. Cold resistance closely tied to content of soluble carbohydrates, particularly raffinose. 11. Flowering: flower buds are pre-formed the year before. Complete development and anthesis dependent upon temperature of the flowering year and also, in some cases, upon photoperiod. 12. Pollination: mostly insect-pollinated in alpine regions and even in Arctic, but to a lesser extent. Wind-pollination increasingly more important with increasing latitude. Diptera more important than bees in the Arctic and in the highest mountains. 13. Seed production: opportunistic, and dependent upon temperature during flowering period and latter half of growing season. 14. Vegetative reproduction: by rhizomes, bulbils, or layering. More common and important in Arctic than in alpine areas. 15. Onset of dormancy: triggered by photoperiod, low temperatures, and drought. Dormant plant extremely resistant to low temperatures.     

Nitrogen content and respiration rate in leaves of the Wrangel Island plants

Protein and total nitrogen contents and respiration rate (at 10°C) were estimated in 22 herbaceous species of Wrangel Island (lat. 71° N). Protein nitrogen content and respiration rate in leaves of these plants were found to exceed 1.3- and 2.4-fold the corresponding indices in the temperate zone plants at the same temperature. The relationship between the content of protein nitrogen and respiration in the Wrangel Island species was insignificant (r ² = 0.137), and the authors conclude that the protein content in the northern plants is not the factor determining the respiration rate in particular plant species. It follows that rather than depend on such indirect indices as nitrogen content, the models for carbon cycle in the North should employ direct respiration measurements at natural plant habitats.     

Temperature-related differences in mitochondrial function among clones of the cladoceran Daphnia pulex

This study assessed the thermal sensitivity of mitochondrial respiration in the small crustacean Daphnia pulex. More specifically, we wanted to determine if clones that inhabit different latitudes and habitats showed differences in the thermal sensitivity of their mitochondrial function. The experimental design included two clones from temperate environments (Fence from Ontario and Hawrelak from Alberta) and two clones from subarctic environments (A24 from Manitoba and K154 from Quebec). The integrated mitochondrial function was measured with high-resolution respirometry following whole-animal permeabilization. Mitochondrial respiration was performed under six different temperatures (10, 15, 20, 25, 30, and 35 °C) in the clone Hawrelak and at two temperatures (10 and 20 °C) in the three other clones. In the clone Hawrelak, complexes I and II respiration showed higher sensitivity to temperature variation compared to complex IV respiration. Interestingly, the threshold plot showed no excess capacity of complex IV at 20 °C in this clone. The clones showed significant divergence in the ability to oxidize the complex I and complex IV substrates relative to the maximal oxidative phoshorylation capacity of mitochondria. More importantly, some of the clonal divergences were only detected under low assay temperatures, pointing toward the importance of this parameter in comparative studies. Future and more complex studies on clones from wider environmental gradients will help to resolve the link between mitochondrial function and adaptations of organisms to particular conditions, principally temperature.     

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.     

Foliar respiration acclimation to temperature and temperature variable Q10 alter ecosystem carbon balance

The response of respiration to temperature in plants can be considered at both short‐ and long‐term temporal scales. Short‐term temperature responses are not well described by a constant Q₁₀ of respiration, and longer‐term responses often include acclimation. Despite this, many carbon balance models use a static Q₁₀ of respiration to describe the short‐term temperature response and ignore temperature acclimation. We replaced static respiration parameters in the ecosystem model photosynthesis and evapo‐transpiration (PnET) with a temperature‐driven basal respiration algorithm (Rd_acclim) that accounts for temperature acclimation, and a temperature‐variable Q₁₀ algorithm (Q_10var). We ran PnET with the new algorithms individually and in combination for 5 years across a range of sites and vegetation types in order to examine the new algorithms' effects on modeled rates of mass‐ and area‐based foliar dark respiration, above ground net primary production (ANPP), and foliar respiration–photosynthesis ratios. The Rd_acclim algorithm adjusted dark respiration downwards at temperatures above 18°C, and adjusted rates up at temperatures below 5°C. The Q_10var algorithm adjusted dark respiration down at temperatures below 15°C. Using both algorithms simultaneously resulted in decreases in predicted annual foliar respiration that ranged from 31% at a tall‐grass prairie site to 41% at a boreal coniferous site. The use of the Rd_acclim and Q_10var algorithms resulted in increases in predicted ANPP ranging from 18% at the tall‐grass prairie site to 38% at a warm temperate hardwood forest site. The new foliar respiration algorithms resulted in substantial and variable effects on PnETs predicted estimates of C exchange and production in plants and ecosystems. Current models that use static parameters may over‐predict respiration and subsequently under‐predict and/or inappropriately allocate productivity estimates. Incorporating acclimation of basal respiration and temperature‐sensitive Q₁₀ have the potential to enhance the application of ecosystem models across broad spatial scales, or in climate change scenarios, where large temperature ranges may cause static respiration parameters to yield misleading results.     

Photosynthesis and respiration in bladelets of Ecklonia cava Kjellman (Laminariales, Phaeophyta) in two localities with different temperature conditions

Characteristics of photosynthesis and respiration of bladelets were compared between Ecklonia cava Kjellman sporophytes growing in a warmer temperate locality (Tei, Kochi Pref., southern Japan) and in a cooler temperate locality (Nabeta, Shizuoka Pref., central Japan). Photosynthesis and respiration were measured with a differential gas-volumeter (Productmeter). In photosynthesis-light curves at 20°C, the rate of net photosynthesis was almost the same at light intensities lower than 25 μmol m⁻² s⁻¹ and the light-saturation occurred at 200–400 μmol m⁻²s⁻¹ in plants of both localities. The light-saturated net photosynthetic rates were higher in winter and spring than in summer and autumn in both plants. The optimum temperature for net photosynthesis at 400 μmol m⁻²s⁻¹ was 27°C throughout the year in the Tei plant and 25–27°C in the Nabeta plant. The decrease of net photosynthetic rates in the supraoptimal temperature range up to 29°C was sharper in winter and spring than in summer and autumn in both plants, being smaller in the Tei plant than in the Nabeta plant in all seasons. The dark respiration rate always increased with water temperature rise in both plants. No clear differences were found in the dark respiration rate between Tei and Nabeta plants except that when measured against dry weight, the Tei plant showed a slightly lower rate as compared with the Nabeta plant.     

Effects of temperature on complexes I and II mediated respiration,ROS generation and oxidative stress status in isolated gill mitochondria of the mud crab Scylla serrata

Effects of fluctuations in habitat temperature (18–30°) on mitochondrial respiratory behavior and oxidative metabolic responses in the euryhaline ectotherm Scylla serrata are not fully understood. In the present study, effects of different temperatures ranging from 12 to 40 °C on glutamate and succinate mediated mitochondrial respiration, respiratory control ratio (RCR), ATP generation rate, ratio for the utilization of phosphate molecules per atomic oxygen consumption (P/O), levels of lipid peroxidation and H₂O₂ in isolated gill mitochondria of S. serrata are reported. The pattern of variation in the studied parameters was similar for the two substrates at different temperatures. The values recorded for RCR (≥3) and P/O ratio (1.4–2.7) at the temperature range of 15–25 °C were within the normal range reported for other animals (3–10 for RCR and 1.5–3 for P/O). Values for P/O ratio, ATP generation rate and RCR were highest at 18 °C when compared to the other assay temperatures. However, at low and high extreme temperatures, i.e. at 12 and 40 °C, states III and IV respiration rates were not clearly distinguishable from each other indicating that mitochondria were completely uncoupled. Positive correlations were noticed between temperature and the levels of both lipid peroxidation and H₂O₂. It is inferred that fluctuations on either side of ambient habitat temperature may adversely influence mitochondrial respiration and oxidative metabolism in S. serrata. The results provide baseline data to understand the impacts of acute changes in temperature on ectotherms inhabiting estuarine or marine environments.     

Interactive Effects of CO2, Temperature,Irradiance, and Nutrient Limitation on the Growth and Physiology of the Marine Diatom Thalassiosira pseudonana (Coscinodiscophyceae)

The marine diatom Thalassiosira pseudonana was grown in continuous culture systems to study the interactive effects of temperature, irradiance, nutrient limitation, and the partial pressure of CO₂ (pCO₂) on its growth and physiological characteristics. The cells were able to grow at all combinations of low and high irradiance (50 and 300 μmol photons · m⁻² · s⁻¹, respectively, of visible light), low and high pCO₂ (400 and 1,000 μatm, respectively), nutrient limitation (nitrate-limited and nutrient-replete conditions), and temperatures of 10–32°C. Under nutrient-replete conditions, there was no adverse effect of high pCO₂ on growth rates at temperatures of 10–25°C. The response of the cells to high pCO₂ was similar at low and high irradiance. At supraoptimal temperatures of 30°C or higher, high pCO₂ depressed growth rates at both low and high irradiance. Under nitrate-limited conditions, cells were grown at 38 ± 2.4% of their nutrient-saturated rates at the same temperature, irradiance, and pCO₂. Dark respiration rates consistently removed a higher percentage of production under nitrate-limited versus nutrient-replete conditions. The percentages of production lost to dark respiration were positively correlated with temperature under nitrate-limited conditions, but there was no analogous correlation under nutrient-replete conditions. The results suggest that warmer temperatures and associated more intense thermal stratification of ocean surface waters could lower net photosynthetic rates if the stratification leads to a reduction in the relative growth rates of marine phytoplankton, and at truly supraoptimal temperatures there would likely be a synergistic interaction between the stresses from temperature and high pCO₂ (lower pH).     

LIGHT AND TEMPERATURE AS FACTORS REGULATING SEASONAL GROWTH AND DISTRIBUTION OF ULOTHRIX ZONATA (ULVOPHYCEAE)1

Ulothrix zonata (Weber and Mohr) Kütz. is an unbranched filamentous green alga found in rocky littoral areas of many northern lakes. Field observations of its seasonal and spatial distribution indicated that it should have a low temperature and a high irradiance optimum for net photosynthesis, and at temperatures above 10°C it should show an increasingly unfavorable energy balance. Measurements of net photosynthesis and respiration were made at 56 combinations of light and temperature. Optimum conditions were 5°C and 1100 μE·m^?2·s^?1 at which net photosynthesis was 16.8 mg O₂·g^?1·h^?1. As temperature increased above 5° C optimum irradiance decreased to 125 μE·m^?2·s^?1 at 30°C. Respiration rates increased with both temperature and prior irradiance. Light-enhanced respiration rates were significantly greater than dark respiration rates following irradiance exposures of 125 μE·m^?2·s^?1 or greater. Polynomials were fitted to the data to generate response surfaces. Polynomial equations represent statistical models which can accurately predict photosynthesis and respiration for inclusion in ecosystem models.     

Latitudinal gradients in some,but not all,avian life history traits extend into the Arctic

Latitudinal variation in avian life history strategies is well documented. Clutch size and nest success tend to increase with latitude, whereas longevity and developmental periods have been argued to decrease with latitude. However, these patterns are largely based on interspecific comparisons of species breeding at tropical and temperate latitudes. We compared the life history of Yellow Warblers Setophaga petechia breeding in arctic habitat at the northern extent of their range, in Inuvik, NWT (68°N), Canada, with those breeding in temperate habitat in Revelstoke, BC (50°N), and use data from 21 populations spanning 0–68°N to evaluate latitudinal trends in life history traits from tropical to arctic habitats. Females breeding in Inuvik laid first clutches that were slightly (although not significantly) larger and had higher nest success, which resulted in higher annual productivity compared with their low- latitude counterparts. Apparent adult survival rates were only marginally lower in Inuvik than in Revelstoke, whereas incubation and nestling periods in the arctic were similar to our temperate site. When comparing life history traits across the Yellow Warbler breeding range, we observed increases in clutch sizes and nest success with increasing latitude that appeared to be associated with declines in adult survival, though this relationship was weakened by the addition of our arctic site. We detected more moderate declines in incubation and nestling periods with increasing latitude. As we observed latitudinal variation in some life history traits, but not a consistent transition of traits associated with a shift from a slow to fast life history from tropical to arctic latitudes, our study suggests that the expectation for a general shift in life history traits may be over-simplified.     

Effect of respiratory homeostasis on plant growth in cultivars of wheat and rice

Some plants have the ability to maintain similar respiratory rates (measured at the growth temperature), even when grown at different temperatures, a phenomenon referred to as respiratory homeostasis. The underlying mechanisms and ecological importance of this respiratory homeostasis are not understood. In order to understand this, root respiration and plant growth were investigated in two wheat cultivars (Triticum aestivum L. cv. Stiletto and cv. Patterson) with a high degree of homeostasis, and in one wheat cultivar (T. aestivum L. cv. Brookton) and one rice cultivar (Oryza sativa L. cv. Amaroo) with a low degree of homeostasis. The degree of homeostasis (H) is defined as a quantitative value, which occurs between 0 (no acclimation) and 1 (full acclimation). These plants were grown hydroponically at constant 15 or 25 °C. A good correlation was observed between the rate of root respiration and the relative growth rates (RGR) of whole plant, shoot or root. The plants with high H showed a tendency to maintain their RGR, irrespective of growth temperature, whereas the plants with low H grown at 15 °C showed lower RGR than those grown at 25 °C. Among several parameters of growth analysis, variation in net assimilation rate per shoot mass (NAR_m) appeared to be responsible for the variation in RGR and rates of root respiration in the four cultivars. The plants with high H maintained their NAR_m at low growth temperature, but the plants with low H grown at 15 °C showed lower NAR_m than those grown at 25 °C. It is concluded that respiratory homeostasis in roots would help to maintain growth rate at low temperature due to a smaller decrease in net carbon gain at low temperature. Alternatively, growth rate per se may control the demand of respiratory ATP, root respiration rates and sink demands of photosynthesis. The contribution of nitrogen uptake to total respiratory costs was also estimated, and the effects of a nitrogen leak out of the roots and the efficiency of respiration on those costs are discussed.     

An Analysis of Plant Growth and its Control in Arctic Environments

The relative growth-rate of plants grown on a vermiculite culturemedium in an arctic climate during the growing season was abouta quarter of that of comparable plants on the same medium ina temperate climate. In both climates the relative growth-ratewas lower on natural soils than on vermiculite. Net assimilationrates and, to a lesser extent, leaf-area ratios were depressedby arctic climates and soils. Net assimilation rates of seven species in various habitatsin two arctic regions were about 0.1–0.3g dm^–2wk^–1.Previous suggestions that net assimilation rates in arctic regionsequal or exceed those in temperate regions are attributed tomisinterpretation of data or to inadequate methods. There is evidence that the depression of net assimilation ratesin arctic regions is due to the low temperatures, which, especiallywhen associated with soil nitrogen deficiency, reduce the rateat which assimilates are used in respiration and new growth;this causes sugars to accumulate to levels at which they depressassimilation.     

Homeoviscous and functional adaptations of mitochondrial membranes to growth temperature in soybean seedlings

The present study investigated whether the cold‐sensitive character of soybean is reflected at the level of mitochondrial membranes. When exposed to an increase of temperature (from 25 to 35 °C), mitochondrial membranes were characterized by a higher phosphatidylcholine : phosphatidylethanolamine ratio and a lower content in 18 : 3 fatty acid. After a reduction of temperature (from 25 to 18 °C) the opposite changes were found. Lipid lateral diffusion and local microviscosity appeared to be comparable in mitochondria from plantlets grown at 25 or 35 °C when assayed at the respective growth temperatures. Some functional aspects (cytochrome c oxidase activity or membrane conductance) tended to this behaviour whereas others (respiration rate or maximum membrane potential) did not. On the other hand, membranes from plants grown at 18 °C were more rigid. Moreover, as illustrated by cytochrome c oxidase activity or respiration rate, functional measurements suggested that these membranes were less active at this temperature. Thus the dynamic characteristics and functional properties measured in mitochondrial membranes were in favour of an adaptive trend at 35 °C, but not at 18 °C despite changes in lipid composition, in accordance with the cold‐sensitive character of the plant.     

Genetic differentiation of high-temperature tolerance in the kelp Undaria pinnatifida sporophytes from geographically separated populations along the Pacific coast of Japan

The kelp Undaria pinnatifida has a widespread latitudinal range in Japan, with populations exposed to very different temperature regimes. To test the hypothesis that U. pinnatifida exhibits genetic differentiation in its temperature response, juvenile sporophytes from a warmer location (Naruto, southern Japan) and two colder locations (Okirai Bay and Matsushima Bay, northern Japan) were collected and transplanted to long lines, cultivated under the environmental conditions in Matsushima Bay. These plants were bred using successive self-crossing methods for three generations and the characteristics of photosynthesis, growth, survival, and nitrogen contents of the third-generation juvenile sporophytes (2–3 cm) then were measured and compared. The plants from Naruto showed significantly higher photosynthetic activities and respiration than those from the northern populations at warmer temperatures of 20–35°C. The juvenile sporophytes from all three locations had similar growth rates below 18°C, but significant differences were observed at 18–24°C. The optimum temperatures for growth were 14–16°C in plants that originated from Okirai Bay and Matsushima Bay and 18°C in plants that originated from Naruto. These results reflected the differences in latitude. Dead plants were observed at high temperatures of 22 and 24°C in the northern population plants, whereas no plants from Naruto died. Juvenile sporophytes from Naruto exhibited the greatest capacity to accumulate high nitrogen reserves. These results suggest that the differences in high-temperature tolerance in juvenile U. pinnatifida sporophytes from geographically separated populations are due to genetic differentiation rather than phenotypic plasticity.     

Microclimate and production of peat moss Sphagnum palustre L. in the warm‐temperate zone

Sphagnum palustre L. is one of the few Sphagnum species distributed in the warm‐temperate zone. To elucidate the mechanisms that enable S. palustre to maintain its productivity under warm climatic conditions, we examined the temperature conditions and photosynthetic characteristics of this species in a lowland wetland in western Japan. Moss temperatures during the daytime were much lower than the air temperature, particularly during summer. The optimum temperature for the net photosynthetic rate was approximately 20°C, irrespective of the season, but summer and autumn samples maintained high rates at higher temperatures as well. The net photosynthetic rate at near light saturation was much higher during summer–autumn than during spring–winter. A model estimation in which net production was calculated from the photosynthetic characteristics and microclimatic data showed that both the low temperature of the moss colony and the seasonal shift in photosynthetic characteristics are among the mechanisms that enable this species to maintain its productivity under warm climatic conditions.     

Effects of constant and fluctuating temperature on time to budburst in Betula pubescens and its relation to bud respiration

 Effects of fluctuating and constant temperatures on budburst time, and respiration in winter buds were studied in Betula pubescens Ehrh. Dormant seedlings were chilled at 0°C for 4 months and then allowed to sprout in long days (LD, 24 h) at constant temperatures of 6, 9, 12, 15, 18 and 21°C, and at diurnally fluctuating temperatures (12/12 h, LD 24 h) with means of 9, 12, 15 and 18°C. No difference in thermal time requirements for budburst was found between plants receiving constant and fluctuating temperatures. The base temperature for thermal time accumulation was estimated to 1°C. Respiration in post-dormant (dormancy fully released) excised winter buds from an adult tree increased exponentially with temperature and was 20 times as high at 30°C than at 0°C. However, respiration in buds without scales was 30% higher at 0°C, and it was 2.7 times higher at 24°C than in intact buds. Thus, the tight bud scales probably constrain respiration and growth and are likely to delay budburst in spring. Arrhenius plots of the respiration data were biphasic with breaks at 13–15°C. However, this phase transition is unlikely to be associated with chilling sensitivity since the present species is hardy and adapted to a boreal climate. Received: 10 January 1997 / Accepted: 23 June 1997     

Whole plant respiration and photosynthesis of wheat under increased CO2 concentration and temperature: long-term vs. short-term distinctions for modelling

Short- and long-term effects of elevated CO₂ concentration and temperature on whole plant respiratory relationships are examined for wheat grown at four constant temperatures and at two CO₂ concentrations. Whole plant CO₂ exchange was measured on a 24 h basis and measurement conditions varied both to observe short-term effects and to determine the growth respiration coefficient (r_g), dry weight maintenance coefficient (r_m), basal (i.e. dark acclimated) respiration coefficient (r_g), and 24 h respiration:photosynthesis ratio (R:P). There was no response of r_g to short-term variation in CO2 concentration. For plants with adequate N supply, r_g was unaffected by the growth-CO₂ despite a 10% reduction in the plant's N concentration (%N). However, r_m was decreased 13%, and r_b was decreased 20% by growth in elevated CO₂ concentration relative to ambient. Nevertheless, R:P was not affected by growth in elevated CO₂. Whole plant respiration responded to short-term variation of ± 5 °C around the growth temperature with low sensitivity (Q₁₀= 1.8 at 15 °C, 1.3 at 30 °C). The shape of the response of whole plant respiration to growth temperature was different from that of the short term response, being a slanted S-shape declining between 25 and 30 °C. While r_m, increased, r_g decreased when growth temperature increased between 15 and 20 °C. Above 20 °C r_m became temperature insensitive while r_g increased with growth temperature. Despite these complex component responses, R:P increased only from 0.40 to 0.43 between 15° and 30 °C growth temperatures. Giving the plants a step increase in temperature caused a transient increase in R:P which recovered to the pre-transient value in 3 days. It is concluded that use of a constant R:P with respect to average temperature and CO₂ concentration may be a more simple and accurate way to model the responses of wheat crop respiration to ‘climate change’ than the more complex and mechanistically dubious functional analysis into growth and maintenance components.     

A comparison of the water balance characteristics of temperate and tropical fly pupae

Abstract Water balance characteristics of temperate zone fly pupae are compared with the characteristics of flies inhabiting the tropics. The flies, all of which were reared without diapause, had very similar equilibrium weights that were quite high (a_v 0.90-0.92), thus implying a limited capacity to absorb water from a subsaturated atmosphere. Likewise, the critical transition temperatures (CTT) were nearly the same for all the flies. Net transpiration rates at 20^oC are a function of size, but the rate is less size dependent as temperature increases. When water loss is examined across a broad temperature range, as described by activation energies, it is apparent that the tropical flies lose water at a greater rate than their temperate zone counterparts. Activation energy may be a good parameter to use in evaluating habitat preference and suitability for a species because it describes water loss as a function of temperature, and thus is likely to be a good indicator of the insect's response to the fluctuating temperatures that occur naturally.