Temperature and water regulation of gas exchange of Opuntia polyacantha

Summary Opuntia polyacantha was collected from the shortgrass prairie in Colorado. Carbon dioxide and water vapor exchange was monitored in plants pretreated and analyzed under cool temperatures (20/15°C) and warm temperatures (35/15°C). Well watered plants under a 35/15 thermoperiod supported the fixation of atmospheric CO₂ during the night, early morning, and late afternoon. Plants under a 20/15 thermoperiod exhibited CO₂ uptake only during the afternoon. The fixation of CO₂ at night could be stimulated or induced by decreasing the night temperature. Plants from which water was withheld two or four weeks showed a decline in CO₂ fixation with the uptake at night exhibiting the greatest sensitivity. Under conditions of water stress the enhancement of CO₂ uptake at night by cool night temperatures was largely lost. Plants water stressed for 4 weeks recovered rapidly upon rewatering under warm or cool temperatures. Rates of CO₂ fixation were comparable to well watered plants within 24 h. The effects of temperature and water stress on gas exchange are compared to the in situ growth pattern of O. polyacantha and contrasted with the regulation of gas exchange observed in C₃ and C₄ grasses of the shortgrass prairie.This research was supported by funds from NSF Grants BMS 74-07894, GB-31862X, and GB-41233X     

Dynamic photo-inhibition and carbon gain in a C4 and a C3 grass native to high latitudes

C₄ plants are rare in the cool climates characteristic of high latitudes and altitudes, perhaps because of an enhanced susceptibility to photo‐inhibition at low temperatures relative to C₃ species. In the present study we tested the hypothesis that low‐temperature photo‐inhibition is more detrimental to carbon gain in the C₄ grass Muhlenbergia glomerata than the C₃ species Calamogrostis Canadensis. These grasses occur together in boreal fens in northern Canada. Plants were grown under cool (14/10 °C day/night) and warm (26/22 °C) temperatures before measurement of the light responses of photosynthesis and chlorophyll fluorescence at different temperatures. Cool growth temperatures led to reduced rates of photosynthesis in M. glomerata at all measurement temperatures, but had a smaller effect on the C₃ species. In both species the amount of xanthophyll cycle pigments increased when plants were grown at 14/10 °C, and in M. glomerata the xanthophyll epoxidation state was greatly reduced. The detrimental effect of low growth temperature on photosynthesis in M. glomerata was almost completely reversed by a 24‐h exposure to the warm‐temperature regime. These data indicate that reversible dynamic photo‐inhibition is a strategy by which C₄ species may tolerate cool climates and overcome the Rubisco limitation that is prevalent at low temperatures in C₄ plants.     

PHOTOSYNTHETIC SENSITIVITY TO TEMPERATURE IN POPULATIONS OF TWO C4 BOUTELOUA (POACEAE) SPECIES NATIVE TO DIFFERENT ALTITUDES

The relationships between photosynthesis, flowering, and growth temperatures were examined experimentally in four populations of the C₄ grass genus Bouteloua. Field-collected plants were grown under two temperature regimes, cool (20 C day/6 C night) and warm (30/16), representative of the extreme populations. Populations collected from the warm climates had significantly lower photosynthetic capacity when grown in the cool chamber relative to the warm chamber, while photosynthetic capacity in the cool climate populations did not differ between the growth conditions. Additionally, exposure to a 2-day cold temperature treatment (10/-2), representative of late-season frosts in high altitude sites, resulted in further reductions in photosynthesis in the warm climate plants, but not in the cool climate plants. This effect was greater for plants grown in the cool growth chamber. Flowering was reduced by 70% in the warm climate plants grown in the cool chamber, and was correlated with photosynthetic inhibition following the short-term cold temperature treatment. These results indicate that genetic differentiation for photosynthetic temperature sensitivity has occurred in the cool climate populations, and that long-term exposure to cool temperatures coupled with short-term relatively extreme low temperatures results in greater photosynthetic inhibition in nontolerant populations.     

A correlation between photosynthetic temperature adaptation and seasonal phenology patterns in the shortgrass prairie

Summary The temperatures at which chlorophyll fluorescence yield is substantially increased and the temperatures at which the quantum yield for CO₂ uptake is irreversibly inhibited were measured for three shortgrass prairie species. The experimental taxa include, a cool season species (Agropyron smithii), a warm season species (Bouteloua gracilis), and a species which grows throughout the cool and warm seasons (Carex stenophylla). Agropyron smithii exhibited lower high temperature damage thresholds (43°C in cool grown plants, 46°C in warm grown plants), relative to the other two species. Bouteloua gracilis exhibited the highest tolerance to high temperature, with threshold values being 44–49°C for cool grown plants and 53–55°C for warm grown plants. Carex stenophylla exhibited threshold values which were intermediate to the other two species (43–47°C for cool grown plants, and 51–53°C for warm grown plants). Seasonal patterns in the fluorescence rise temperatures of field grown plants indicated acclimation to increased temperatures in all three species. The results demonstrate a correlation between the high temperature thresholds for damage to the photosynthetic apparatus, and in situ seasonal phenology patterns for the three species.     

Optimum leaf size predicted by a novel leaf energy balance model incorporating dependencies of photosynthesis on light and temperature

To clarify relationships between leaf size and the environment variables, we constructed an energy balance model for a single leaf incorporating Leuning’s stomatal conductance model and Farquhar’s leaf photosynthesis model. We ran this model for various environmental conditions paying particular attention to the leaf boundary layer. The leaf size maximizing the rate of photosynthesis per unit leaf area (A) at a high irradiance differed depending on the air temperature. In warm environments, A increased with decrease in leaf size, whereas in cool environments, there was the leaf size maximizing A. With the increase in leaf size, the CO₂ concentration inside the leaf (C _i) decreased and the leaf temperature increased, both due to lower boundary layer conductance. At low air temperatures, the negative effect of low C _i on A in large leaves was compensated by the increase in leaf temperature towards the optimum temperature for A. This balance determined the optimum leaf size for A at low air temperatures. With respect to water use efficiency, large leaves tended to be advantageous, especially in cool environments at low-to-medium irradiances. Some temperature-dependent trends in leaf size observed in nature are discussed based on the present results.     

Pre‐zygotic parental environment modulates seed longevity

The potential for the pre‐zygotic plant growth environment to play a role in determining seed longevity was investigated for a species that inhabits arid to semi‐arid Australia. Seed longevity is particularly important for wild populations in fluctuating environments because the longer a seed‐lot is able to survive in the soil seed bank the more likely it is to buffer the population from unpredictable environments. Thus Wahlenbergia tumidifructa plants received wet or dry soil moisture within a warm or cool glasshouse until flowering. Seeds subsequently produced by flowers that opened on the day that plants were moved to a common environment were collected at maturity and longevity assessed by controlled ageing at 60% relative humidity and 45°C. Mean seed longevity was similar for seeds produced by plants that grew in warm‐wet, warm‐dry and cool‐dry conditions (P₅₀ of about 20 days), but extended for plants in cool‐wet conditions (P₅₀ = 41.7 days). Cool temperatures resulted in seeds with a wider distribution of lifespans (σ = 20 days) than warm conditions (σ = 12 days); the large σ caused the extended P₅₀ for cool‐wet plants, but not cool‐dry as a result of a concomitant reduction in initial seed germination (K_i). After moving to the common environment, all plants generated new vegetative material, which went on to produce seeds with similar longevity (P₅₀ approx. 20 days) irrespective of original environment. Visible phenotypic responses of the parent to environmental conditions correlated with longevity and quality parameters of the progeny seeds, suggesting that a parental effect modified seed longevity. Our study provides novel empirical data showing that environmental conditions expected under climate change scenarios may potentially cause seed longevity to decline for a species that inhabits arid to semi‐arid Australia. These negative impacts on population buffering may weaken the storage effect mechanism of species coexistence in fluctuating environments.     

Infrared Energy as a Factor in Controlled Environments

The proportion of visible to infrared radiation varies in different growth chambers. Whether this might affect leaf temperature and plant growth was investigated in chambers with equal visible radiation. In one chamber infrared energy was half the total, while in two chambers it was 75% of the total. Photoperiods were 14 hours and day and night temperatures 25° and 20°C, respectively. Warm weather species tested were Zea mays, Phaseolus vulgaris, Gossypium hirsutum, Glycine max, and Sorghum vulgare. High infrared did not increase the leaf temperatures of Sorghum vulgare, but growth was better than under low infrared. In the other 4 species, slightly higher leaf temperatures were observed, but growth was not significantly increased by high infrared. Of the cool weather species, Pisum sativum L. (Alaska and Wando) and Vicia faba L., grew less; Avena saliva L. grew equally; and Brassica oleracea L. var. capitata grew better in high infrared. Leaf temperatures of these cool weather species were generally below ambient and were not appreciably affected by the proportion of infrared. The CO₂ was uncontrolled in one high infrared chamber and was 400 μl CO₂ liter or more. Except for G. max and P. vulgaris, the growth of the warm weather species was not significantly affected; however, all cool weather species grew best in this chamber. A sparing effect from infrared damage is induced by high CO₂.     

Acclimation of photosynthesis to temperature in eight cool and warm climate herbaceous C3 species: Temperature dependence of parameters of a biochemical photosynthesis model

To determine how parameters of a Farquhar-type photosynthesis model varied with measurement temperature and with growth temperature, eight cool and warm climate herbaceous crop and weed species were grown at 15 and 25 °C and single leaf carbon dioxide and water vapor exchange rates were measured over the range of 15 – 35 °C. Photosynthetic parameters examined were the initial slope of the response of assimilation rate (A) to substomatal carbon dioxide concentration (C_i), A at high C_i, and stomatal conductance. The first two measurements allow calculation of V_Cmax, the maximum rate of carboxylation of ribulose bisphosphate carboxylase and J_max, the maximum rate of photosynthetic electron transport, of Farquhar-type photosynthesis models. In all species, stomatal conductance increased exponentially with temperature over the whole range of 15 – 35 °C, even when A decreased at high measurement temperature. There were larger increases in conductance over this temperature range in the warm climate species (4.3 ×) than in the cool climate species (2.5 ×). The initial slope of A vs. C_i exhibited an optimum temperature which ranged from 20 to 30 °C. There was a larger increase in the optimum temperature of the initial slope at the warmer growth temperature in the cool climate species than in the warm climate species. The optimum temperature for A at high C_i ranged from 25 to 30 °C among species, but changed little with growth temperature. The absolute values of both the initial slope of A vs. C_i and A at high C_i were increased about 10% by growth at the warmer temperature in the warm climate species, and decreased about 20% in the cool climate species. The ratio of J_max — V_Cmax normalized to 20 °C varied by more than a factor of 2 across species and growth temperatures, but differences in the temperature response of photosynthesis were more related to variation in the temperature dependencies of J_max and V_Cmax than to the ratio of their normalized values.This revised version was published online in October 2005 with corrections to the Cover Date.     

PHYSIOLOGICAL RESPONSES OF ECKLONIA RADIATA (LAMINARIALES) TO A LATITUDINAL GRADIENT IN OCEAN TEMPERATURE1

We tested the ability of sporophytes of a small kelp, Ecklonia radiata (C. Agardh) J. Agardh, to adjust their photosynthesis, respiration, and cellular processes to increasingly warm ocean climates along a latitudinal gradient in ocean temperature (～4°C). Tissue concentrations of pigment and nutrients decreased with increasing ocean temperature. Concurrently, a number of gradual changes in the metabolic balance of E. radiata took place along the latitudinal gradient. Warm‐acclimatized kelps had 50% lower photosynthetic rates and 90% lower respiration rates at the optimum temperature than did cool‐acclimatized kelps. A reduction in temperature sensitivity was also observed as a reduction in Q₁₀‐values from cool‐ to warm‐acclimatized kelps for gross photosynthesis (Q₁₀: 3.35 to 1.45) and respiration (Q₁₀: 3.82 to 1.65). Respiration rates were more sensitive to increasing experimental temperatures (10% higher Q₁₀‐values) than photosynthesis and had a higher optimum temperature, irrespective of sampling location. To maintain a positive carbon balance, E. radiata increased the critical light demand (E_c) exponentially with increasing experimental temperature. The temperature dependency of E_c was, however, weakened with increasing ocean temperature, such that the critical light demand was relaxed in kelp acclimated to higher ocean temperatures. Nevertheless, calculations of critical depth limits suggested that direct effects of future temperature increases are unlikely to be as strong as effects of reduced water clarity, another globally increasing problem in coastal areas.     

Stream temperature and the potential growth and survival of juvenile Oncorhynchus mykiss in a southern California creek

1. We asked whether an increase in food supply in the field would increase the ability of fish populations to withstand climate warming, as predicted by certain bioenergetic models and aquarium experiments. 2. We subsidised the in situ food supply of wild juvenile steelhead (Oncorhynchus mykiss) in a small stream near the species’ southern limit. High‐quality food (10% of fish biomass per day) was added to the drift in eight in‐stream enclosures along a naturally‐occurring thermal gradient. 3. The temperatures during the experiment were well below the upper thermal limit for the species (means of enclosures ranged from 15.1 to 16.5 °C). Food supplements had no discernible effect on survival, but raised mean (± SD) specific growth rate substantially, from 0.038 ± 0.135 in controls to 2.28 ± 0.51 in feeding treatments. Food supplements doubled the variation in growth among fish. 4. The mean and variance of water temperature were correlated across the enclosures, and were therefore transformed into principal component scores T₁ (which expressed the stream‐wide correlation pattern) and T₂ (which expressed local departures from the pattern). Even though T₁ accounted for 96% of the variation in temperature mean and variance, it was not a significant predictor of fish growth. T₂ was a significant predictor of growth. The predicted time to double body mass in an enclosure with a large T₂ score (cool‐variable) was half that in an enclosure with a low T₂ score (warm‐stable). 5. Contrary to expectation, temperature effects were neutral, at least with respect to the main axis of variation among enclosures (cool‐stable versus warm‐variable). Along the orthogonal axis (cool‐variable versus warm‐stable), the effect was opposite from expectations, probably because of temperature variation. Subtle patterns of temperature heterogeneity in streams can be important to potential growth of O. mykiss.     

The subdominant status of Echinocereus viridiflorus and Mammillaria vivipara in the shortgrass prairie: The role of temperature and water effects on gas exchange

Summary The subdominant CAM species, Echinocereus viridiflorus and Mammillaria vivipara, collected from the shortgrass prairie in northeastern Colorado were pretreated and analyzed for gas exchange under cool temperatures (20/15°C) and warm temperatures (35/15°C). Well watered plants of both species under a 35/15°C thermoperiod fixed atmospheric CO₂ during the night and early moring. Echinocereus viridiflorus grown and analyzed at 20/15°C fixed CO₂ during the night, early morning and late afternoon but total carbon gain over a 24 h period is less than when grown and analyzed under the 35/15°C thermoperiod. Mammillaria vivipara grown and analyzed at 20/15°C assimilates CO₂ at low rates during all parts of a 24 h period with the greatest CO₂ fixation rates occuring from midday to late afternoon. The total carbon gain under the 20/15°C thermoperiod is less than that for this species under the 35/15°C thermoperiod. Decreasing the night temperature of plants grown under the warm conditions to 10°C or 5°C results in a depression of the night CO₂ fixation in both species. E. viridiflorus from the cool growth conditions showed an enhancement of the CO₂ uptake during the night, early morning and late afternoon when subjected to the cooler night temperatures (10°C and 5°C). The CO₂ uptake of M. vivipara grown at 20/15°C shows an enhancement during the night and early morning while the CO₂ fixation during midday and late afternoon is slightly depressed under cool night temperatures (10° and 5°C). Under the 35/15°C thermoperiod both species exhibit depressed rates of CO₂ fixation during the night and early morning when water stressed. Plants of both species grown under the 20/15°C thermoperiod exhibit no net CO₂ fixation following five weeks of water deprivation. Upon rewatering, E. viridiflorus begins to recover its capacity for CO₂ fixation within 24 h under both the warm and cool temperature regimes. However, M. vivipara did not show recovery within 48 h following rewatering under the warm or cool temperature regime. Contrasting the patterns of gas exchange of the subdominant species, E. viridiflorus and M. vivipara, with a dominant CAM species of the shortgrass prairie, Opuntia polyacantha reveals significant differences that may well dictate the role of these species in this ecosystem. E. viridiflorus and M. vivipara have a lower capacity of carbon gain and recovery from water stress than O. polyacantha mainly due to their lack of late afternoon CO₂ uptake. This study suggests that carbon gain plays an important role in limiting E. viridiflorus and M. vivipara in the shortgrass prairie ecosystem.     

Low-temperature photosynthetic performance of a C4 grass and a co-occurring C3 grass native to high latitudes

The photosynthetic performance of C₄ plants is generally inferior to that of C₃ species at low temperatures, but the reasons for this are unclear. The present study investigated the hypothesis that the capacity of Rubisco, which largely reflects Rubisco content, limits C₄ photosynthesis at suboptimal temperatures. Photosynthetic gas exchange, chlorophyll a fluorescence, and the in vitro activity of Rubisco between 5 and 35 °C were measured to examine the nature of the low‐temperature photosynthetic performance of the co‐occurring high latitude grasses, Muhlenbergia glomerata (C₄) and Calamogrostis canadensis (C₃). Plants were grown under cool (14/10 °C) and warm (26/22 °C) temperature regimes to examine whether acclimation to cool temperature alters patterns of photosynthetic limitation. Low‐temperature acclimation reduced photosynthetic rates in both species. The catalytic site concentration of Rubisco was approximately 5.0 and 20 µmol m^?2 in M. glomerata and C. canadensis, respectively, regardless of growth temperature. In both species, in vivo electron transport rates below the thermal optimum exceeded what was necessary to support photosynthesis. In warm‐grown C. canadensis, the photosynthesis rate below 15 °C was unaffected by a 90% reduction in O₂ content, indicating photosynthetic capacity was limited by the capacity of P_i‐regeneration. By contrast, the rate of photosynthesis in C. canadensis plants grown at the cooler temperatures was stimulated 20–30% by O₂ reduction, indicating the P_i‐regeneration limitation was removed during low‐temperature acclimation. In M. glomerata, in vitro Rubisco activity and gross CO₂ assimilation rate were equivalent below 25 °C, indicating that the capacity of the enzyme is a major rate limiting step during C₄ photosynthesis at cool temperatures.     

C4 photosynthesis in Spartina townsendii at low and high temperatures

The metabolism of ¹⁴CO₂ in the cool temperate saltmarsh grass Spartina townsendii was investigated in plants grown in their natural habitats at two temperatures. Both in the spring at 10°C and in the late summer at 25°C radioactivity was initially incorporated into the organic acids malate and aspartate and then transferred to 3-phosphoglycerate in the manner characteristic of the C₄ pathway of photosynthesis. Metabolism was not disrupted at the lower temperature as in some C₄ plants. Radioactivity was transferred more slowly from malate into alanine, glycine and serine at 10°C, but sugars were labelled equally at both temperatures.     

The effect of temperature on the development times of eggs,naupliar and copepodite stages of five species of cyclopoid copepods

The duration times of eggs, combined naupliar instars and of the different copepodite stages of five species of cyclopoid copepods — Acanthocyclops robustus, Cyclops vicinus, Diacyclops bicuspidatus, Mesocyclops leuckarti, and Thermocyclops crassus — were investigated at five different temperatures. The five species can be divided in two groups: two species, C. vicinus and D. bicuspidatus, adapted to cold water conditions and three species, A. robustus, M. leuckarti and T. crassus adapted to warm water conditions. The cold water species showed a faster egg development than M. leuckarti and T. crassus at 5–15 °C. The eggs and instars of the warm water species M. leuckarti tend to develop faster than those of the former two species at higher temperatures. A. robustus showed the shortest egg and instar development at 10–25 °C. The warm water species T. crassus produced no eggs at 10 °C and temperatures below. At higher temperatures (20, 25 °C) the egg and instar duration times were similar or longer than those of the other species. When cultured in total darkness a great part of the C_IV respectively C_V copepodites of the summer forms entered arrest and the percentage of copepodites that showed an arrest of development was highest at lowest temperatures. The present results are compared with data from literature and differences are discussed.     

Diel and seasonal variations in the thermal biology of San Cristobal Lava Lizards (Microlophus bivittatus)

Thermal biology, and therefore energy acquisition and survival, of ectotherms can be affected by diel and seasonal patterns of environmental temperatures. Galápagos Lava Lizards live in seasonal environments that are characterized by a warm and wet period when reproductive activity is maximal, and cooler and drier period. With the use of radiotelemetric techniques to record lizard surface temperatures (T_s), we studied the thermal ecology of the San Cristóbal Lava Lizard (Microlophus bivittatus) during both the warm and cool seasons over two years. During the diel activity period and when operative temperatures exceeded T_set-min, at least on rock faces without canopy, 52% or less of the T_s observations fell within the laboratory-determined T_set range (36–40 °C). Therefore, lizards may have avoided very warm midday temperatures in shaded microhabitats and the lag times in changes in T_s values occurred as operative temperatures rose rapidly during late morning warming phase. Lizards effectively thermoregulated during a year with moderate warm season temperatures and during a cool season that was unseasonably warm. In contrast, lizards less effectively thermoregulated during the warmest and coolest years of the study. We did not detect intersexual differences in thermoregulation although males may thermoregulate less effectively than do females during the cool season although we were unable to detect significant differences using our nonparametric statistical techniques.     

Growth and temperature relationships for juvenile fish species in seagrass beds: implications of climate change

The effect of water temperature on growth responses of three common seagrass fish species that co‐occur as juveniles in the estuaries in Sydney (34° S) but have differing latitudinal ranges was measured: Pelates sexlineatus (subtropical to warm temperate: 27–35° S), Centropogon australis (primarily subtropical to warm temperate: 24–37° S) and Acanthaluteres spilomelanurus (warm to cool temperate: below 32° S). Replicate individuals of each species were acclimated over a 7 day period in one of three temperature treatments (control: 22° C, low: 18° C and high: 26° C) and their somatic growth was assessed within treatments over 10 days. Growth of all three species was affected by water temperature, with the highest growth of both northern species (P. sexlineatus and C. australis) at 22 and 26° C, whereas growth of the southern ranging species (A. spilomelanurus) was reduced at temperatures higher than 18° C, suggesting that predicted increase in estuarine water temperatures through climate change may change relative performance of seagrass fish assemblages.     

Seasonal variation of thermoregulatory behaviour in the Hippopotamus (Hippopotamus amphibius)

The hippopotamus (Hippopotamus amphibius) spends more than 12 h a day in the water. Hippos are often submitted to water temperatures that vary with the seasons. We hypothesize that this difference between cool and warm water temperatures leads to variations in behavioural thermoregulation. We recorded the exposure of hippos to sunshine at the beginning and at the end of the dry season. Our results show that (1) sunshine exposure lasted much longer in cool water and (2) sun-bathing occurred during the hottest hours. It is therefore likely that in cool water hippos were cold and expressed an original behaviour of search for heat.     

Tuberization in Potato at High Temperatures: interaction between Shoot and Root Temperatures

Tuber formation in intact potato plants (Solanum tuberosum L.cv. Sebago) was reduced by high shoot or root temperatures andstrongly inhibited when both were high. When both the shootand root temperatures were high, disbudding strongly promotedtuberization. There was a smaller increase with warm roots andcool shoots, but no response with warm shoots and cool roots.When both the shoots and roots were cool, disbudding reducedtuberization. Exogenous GA₃, effectively substituted for thebuds at high temperatures, completely preventing tuberization.In apical cuttings, removal of the terminal bud, but not theroots, reduced the inhibitory effects of high temperatures ontuberization. The experiment indicates that tuber productionmay be controlled by at least three factors: a promoter, whichis not assimilate, produced by the buds at cool temperatures;an inhibitor, derived from the buds, but dependent on warm roottemperatures for its formation; and a second inhibitor derivedfrom the mature leaves and produced in response to warm shoottemperatures. Solanum tuberosumL, potato, tuberization, temperature, disbudding, gibberellic acid     

Membrane and calcium clock mechanisms contribute variably as a function of temperature to setting cardiac pacemaker rate in zebrafish Danio rerio

Here, we show that heart rate in zebrafish Danio rerio is dependent upon two pacemaking mechanisms and it possesses a limited ability to reset the cardiac pacemaker with temperature acclimation. Electrocardiogram recordings, taken from individual, anaesthetised zebrafish that had been acclimated to 18, 23 or 28°C were used to follow the response of maximum heart rate (f_Hmax) to acute warming from 18°C until signs of cardiac failure appeared (up to c. 40°C). Because f_Hmax was similar across the acclimation groups at almost all equivalent test temperatures, warm acclimation was limited to one significant effect, the 23°C acclimated zebrafish had a significantly higher (21%) peak f_Hmax and reached a higher (3°C) test temperature than the 18°C acclimated zebrafish. Using zatebradine to block the membrane hyperpolarisation-activated cyclic nucleotide–gated channels (HCN) and examine the contribution of the membrane clock mechanisms to cardiac pacemaking, f _Hmax was significantly reduced (by at least 40%) at all acute test temperatures and significantly more so at most test temperatures for zebrafish acclimated to 28°C vs. 23°C. Thus, HCN channels and the membrane clock were not only important, but could be modified by thermal acclimation. Using a combination of ryanodine (to block sarcoplasmic calcium release) and thapsigargin (to block sarcoplasmic calcium reuptake) to examine the contribution of sarcoplasmic reticular handling of calcium and the calcium clock, f _Hmax was again consistently reduced independent of the test temperature and acclimation temperature, but to a significantly lesser degree than zatebradine for zebrafish acclimated to both 28 and 18°C. Thus, the calcium clock mechanism plays an additional role in setting pacemaker activity that was independent of temperature. In conclusion, the zebrafish cardiac pacemaker has a limited temperature acclimation ability compared with known effects for other fishes and involves two pacemaking mechanisms, one of which was independent of temperature.     

Seasonal variation of photosynthesis and photosynthetic efficiency in <Emphasis Type="Italic">Phalaenopsis</Emphasis>

Nowadays, a quest for efficient greenhouse heating strategies, and their related effects on the plant’s performance, exists. In this study, the effects of a combination of warm days and cool nights in autumn and spring on the photosynthetic activity and efficiency of Phalaenopsis were evaluated; the latter, being poorly characterised in plants with crassulacean acid metabolism (CAM) and, to our knowledge, not reported before in Phalaenopsis. 24-h CO₂ flux measurements and chlorophyll (Chl) fluorescence analyses were performed in both seasons on Phalaenopsis ‘Hercules’ exposed to relatively constant temperature regimes, 25.5/24.0°C (autumn) and 30/27°C (spring) respectively, and distinctive warm day/cool night temperature regimes, 27/20°C (autumn) and 36/24°C (spring), respectively. Cumulated leaf net CO₂ uptake of the distinctive warm day/cool night temperature regimes declined with 10–16% as compared to the more constant temperature regimes, while the efficiency of carbon fixation revealed no substantial differences in both seasons. Nevertheless, a distinctive warm day/cool night temperature regime seemed to induce photorespiration. Although photorespiration is expected not to occur in CAM, the suppression of the leaf net CO₂ exchange during Phase II and Phase IV as well as the slightly lower efficiency of carbon fixation for the distinctive warm day/cool night temperature regimes confirms the involvement of photorespiration in CAM. A seasonal effect was reflected in the leaf net CO₂ exchange rate with considerably higher rates in spring. In addition, sufficiently high levels of photosynthetically active radiation (PAR) in spring led to an efficiency of carbon fixation of 1.06–1.27% which is about twice as high than in autumn. As a result, only in the case where a net energy reduction between the temperature regimes compensates for the reduction in net CO₂ uptake, warm day/cool night temperature regimes may be recommended as a practical sustainable alternative.