Gas exchange and blood gases of Puna teal (Anas versicolor puna) embryos in the Peruvian Andes

Oxygen consumption, air cell gases, hematology, blood gases and pH of Puna teal (Anas versicolor puna) embryos were measured at the altitude at which the eggs were laid (4150 m) in the Peruvian Andes. In contrast to the metabolic depression described by other studies on avian embryos incubated above 3700 m, O₂ consumption of Puna teal embryos was higher than even that of some lowland avian embryos at equivalent body masses. Air cell O₂ tensions dropped from about 80 toor in eggs with small embryos to about 45 toor in eggs containing a 14-g embryo; simultaneously air cell CO₂ tension rose from virtually negligible amounts to around 26 torr. Arterial and venous O₂ tensions (32–38 and 10–12 toor, respectively, in 12- to 14-g embryos) were lower than described previously in similarly-sized lowland wild avian embryos or chicken embryos incubated in shells with restricted gas exchange. The difference between air cell and arterial O₂ tensions dropped significantly during incubation to a minimum of 11 torr, the lowest value recorded in any avian egg. Blood pH (mean 7.49) did not vary significantly during incubation. Hemoglobin concentration and hematocrits rose steadily throughout incubation to 11.5 g · 100 ml^-1 and 39.9%, respectively, in 14-g embryos.Abbreviations PO₂ partial pressure gradient of O₂ - BM body mass - D diffusion coefficient - G gas conductance (cm³·s^-1·torr^-1) - conductance to water vapor - IP internal pipping of embryos - P _ACO₂ partial pressure of carbon dioxide in air cell - P _AO₂ partial pressure of oxygen in air cell - P _aCO₂ partial pressure of carbon dioxide in arterial blood - P _aCO₂ partial pressure of oxygen in arteries - P _H barometric pressure (torr) - PCO₂ partial pressure of carbon dioxide - P _IO₂ partial pressure in ambiant air - PO₂ partial pressure of oxygen - P _VCO₂ venous carbon dioxide partial pressure - P _VO₂ mixed venous oxygen partial pressure - SE standard error - VO ₂ oxygen consumption     

Similarity of PO2 and PCO2 values in the air cell of eggs of birds and in the alveolar gas of humans at sea level and at high altitude

At the end of incubation, the partial pressures of oxygen and carbon dioxide in the air cell of sea-level avian eggs are similar to those in the expiratory air of adult birds. At high altitude, changes in the permeability of the shell and probably in the embryo metabolism partially compensates the increase in the gas diffusion constant resulting from the low barometric pressure. The aim of this study was to test whether-despite of the adaptive responses of the high altitude avian embryo-the air cell values would be similar to those of the alveolar air of high altitude human natives. Air cell O₂ (48.3±1.6 torr) and CO₂ (20.9±0.85 torr) pressure values were obtained by studying naturally incubated eggs of the Andean gull (Larus serranus)_at 4650m. Sea-level chicken (Gallus gallus) air cell pressure values of O₂ (102.3±2.7 torr) and of CO₂ (43.3±1.3 torr) were obtained from the literature for comparison. Both these values were similar to those found in the alveolar air of humans at sea level (O₂: 104.4±0.4 torr, CO₂:40.1±0.25 torr) and at high altitude (4540 m) (O₂:50.5±0.53 torr, CO₂: 29.1±0.37 torr). Despite very large evolutionary changes in morphology and physiology of the respiratory organs, the head pressure of O₂ that oxygenates the blood keeps a constant value in the pre-pipping avian embryo and in the alveolar air of adult mammals. This constancy holds valid at high altitude.     

Gas exchange and energy metabolism of the ostrich (Struthio camelus) embryo

We measured oxygen consumption ( ) and carbon dioxide emission ( ) rates, air-cell gas partial pressures of oxygen (P_AO₂) and CO₂ (P_ACO₂), eggshell water vapour conductance and energy content of the ostrich (Struthio camelus) egg, ‘true hatchling’ and residual yolk, and calculated RQ and total oxygen consumption ( ) for ostrich eggs incubated at 36.5°C and 25% relative humidity. The pattern showed a drop of approximately 5% before internal pipping. just prior to internal pipping agrees with allometric calculations. Despite the higher incubation temperature compared to other studies, and the resultant shorter incubation duration (42 days), (91.7 l kg⁻¹) was similar to a previously reported value. RQ values during the second half of incubation (approx. 0.68) were lower than expected for lipid catabolism. Prior to internal pipping, P_AO₂ and P_ACO₂ were 98 and 48.3 torr (13.1 and 6.4 kPa), respectively. The growth pattern of the ostrich embryo is different from the typical precocial pattern, showing a time delay in the rapid growth phase. As a result, the lowered overall energy expenditure for tissue maintenance, as compared to other species, is reflected in the low yolk utilization and high residual yolk fraction of the whole hatchling dry mass. These could also result from the relatively short incubation period of the ostrich egg, thereby evading desiccation by excess water loss.     

Incubation water loss,shell conductance,and pore dimensions in Adelie Penguin eggs

Summary In order to understand water loss regulation of bird eggs in very dry climates eggs of the Adelie Penguin were studied at Cape Bird, Ross Island, Antarctica. During incubation 125 g Adelie Penguin eggs lose about 447 mg of water per day, resulting in an overall estimated loss, during 35 days of incubation, of 13% of their initial mass. The eggshell conductance of 13.1 mg H₂O·day^-1·torr^-1 occurs from 9100 pores with an effective radius and pore length of 11 m and 600 m, respectively. In this study the water vapor pressure of the egg was 44 torr, estimated from the egg temperature of 35.9°C. Ambient temperature was-4°C, with an absolute humidity of less than 3 torr, resulting in an overall vapor pressure difference between the egg and the environment of 41 torr. This difference was divided between the egg and nest conductance in a ratio of ca. 1:5.     

Structural and physiological differences between montane and lowland avian eggs and embryos

A few avian species breed at altitudes up to 6500 m. Embryos in eggs laid at high altitudes are confronted with the problem that gases diffuse more rapidly at low barometric pressure than at sea level. Data on birds breeding up to 4500 m indicate that modifications in eggshell structure and embryonic physiology foster successful development in these groups. At moderate altitudes (up to 3600 m), shell conductance to gases (corrected to 760 torr) is decreased in approximate proportion to the reduction in barometric pressure, thus offsetting the increased tendency of gases to diffuse. At altitudes above 4000 m, the conductance is increased above levels at moderate altitudes, thus fostering improvement in oxygen availability, while increasing rates of water and CO2 losses. Above 4000 m, embryonic physiological properties become increasingly important for coping with hypoxic, hypocapnic, and dehydrated conditions inside the shell. Nothing is known about characteristics of eggshells and embryos in eggs laid between 4500 and 6500 m. Despite years of artificial selection, domestic fowl do not breed successfully much above 3000 m. Embryos of domestic fowl appear highly sensitive to the effects of hypoxia.     

Gas fluxes in avian eggs: Driving forces and the pathway for exchange

• 1.1. In this study, we review reported values for fluxes of water vapor and oxygen across the pores in avian eggshells, pore numbers per egg, the changes in O₂ and CO₂ tensions in the air space during development, and the absolute humidity of bird nests in various climates.
• 2.2. With egg mass from 1 to 1500 g as the independent variable we use regression analysis of daily water vapor loss, O₂ uptake at the preinternal pipping (PIP) stage of development, and pore numbers to show that O₂, CO₂ and water vapor fluxes per pore are 68, 50 and 49 μl/day, respectively, independent of egg mass. When these fluxes are divided by the invariant pore conductance previously established by Ar and Rahn (Respir. Physiol. 61, 1–20, 1985), predicted air cell O₂ and CO₂ tensions of ca 100 and 40 Torr just prior to the initiation of lung function are obtained, values which agree well with mean measured gas tensions in 25 species.
• 3.3. Our analysis complements the model proposed by Ar and Rahn, in which pores serve as basic respiratory units for most bird eggs. In this model, pore number per egg is matched to O₂ demand at the PIP stage of development to produce the commonly observed air cell gas tensions. Average, total diffusive water loss in 117 species is 15%, SD 2.6, of initial egg mass. To achieve this value requires the proper combination of pore number, egg temperature and nest water vapor tension; the latter is also a function of nest construction and incubation behavior. Examples of nest absolute humidity are cited for 20 species which incubate in diverse climates with ambient absolute humidities from 4 to 22 Torr. Exceptions to the model are seen in eggs incubated under environmental conditions which are unusual in temperature, humidity, or altitude.

     

Photosynthesis of cotton plants exposed to elevated levels of carbon dioxide in the field

The cotton (Gossypium hirsutum L.) plant responds to a doubling of atmospheric CO₂ with almost doubled yield. Gas exchange of leaves was monitored to discover the photosynthetic basis of this large response. Plants were grown in the field in open-top chambers with ambient (nominally 350 l/l) or enriched (nominally either 500 or 650 l/l) concentrations of atmospheric CO₂. During most of the season, in fully-irrigated plants the relationship between assimilation (A) and intercellular CO₂ concentration (c_i) was almost linear over an extremely wide range of c_i. CO₂ enrichment did not alter this relationship or diminish photosynthetic capacity (despite accumulation of starch to very high levels) until very late in the season, when temperature was somewhat lower than at midseason. Stomatal conductance at midseason was very high and insensitive to CO₂, leading to estimates of c_i above 85% of atmospheric CO₂ concentration in both ambient and enriched chambers. Water stress caused A to show a saturation response with respect to c_i, and it increased stomatal closure in response to CO₂ enrichment. In fully-irrigated plants CO₂ enrichment to 650 l/l increased A more than 70%, but in water-stressed plants enrichment increased A only about 52%. The non-saturating response of A to c_i, the failure of CO₂ enrichment to decrease photosynthetic capacity for most of the season, and the ability of the leaves to maintain very high c_i, form in part the basis for the very large response to CO₂ enrichment.Abbreviations c_a- atmospheric CO₂ concentration - c_i- intercellular CO₂ concentration - A- rate of assimilation of CO₂ - g_s- stomatal conductance to water vapor - g_b- boundary layer conductance to water vapor - g_m- mesophyll conductance to CO₂ - VPD- vapor pressure deficit - _w leaf water potential - L- stomatal limitation to CO₂ uptake     

PO2 and pH changes in the retina of the crab Ocypode ryderi: evidence for aerobic glycolysis

Summary The isolated retina of the terrestrial crab Ocypode ryderi exhibits a pronounced lactate production in spite of being supplied with sufficient O₂ (140 torr). To determine whether this lactate production is caused by hypoxic areas in the tissue or represents aerobic glycolysis, oxygen partial pressure and pH measurements with two-channel glass microelectrodes and additional biochemical analyses were carried out on this organ. Distinct profiles were obtained for O₂ partial pressure and pH inside the tissue. At a depth of 200 m different O₂ partial pressure levels could be observed depending on the O₂ partial pressure in the medium (85 torr at 280 torr and 36 torr at 130 torr, respectively). The extracellular pH displays a similar pattern; it reaches a stable value of 7.15 at 100 m inside the tissue. Lowering bath O₂ partial pressure from 280 torr to about 15 torr (hypoxia) induces a decrease of the O₂ partial pressure in the tissue with different time-courses for different tissue depths. However, hypoxia did not change the extracellular pH. Addition of antimycin A (100 mol · 1^-1) to the medium abolishes the O₂ partial pressure gradient and the delayed recovery of the tissue O₂ partial pressure after hypoxia. These results and the biochemical data suggest that in the crab retina a high glycolytic activity occurs simultaneously with oxydative carbohydrate degradation (aerobic glycolysis).Abbreviations AEC Atkinson energy charge - DC bioelectric potential - dw dry weight - HEPES N-[2-Hydroxyethyl]piperazine-N-[2-ethanesulphonic acid] - PCO₂ carbon dioxide partial pressure - PO₂ oxygen partial pressure - P _tO₂ oxygen partial pressure inside the tissue - P _mO₂ oxygen partial pressure in the medium - pH_t pH inside the tissue - pH_m pH in the superfusion medium     

Effects of variation in total and regional shell conductance on air cell gas tensions and regional gas exchange in chicken eggs

Summary Gas conductance of the shell, rates of O₂ consumption, CO₂ production and air cell gas tensions were measured in pre-internal pipping, 19 day-old chicken eggs that were selected for a wide range in shell conductance. Regional conductance was measured in eggs with partially waxed shells.Surface-specific shell conductance was not uniform over the egg; it was over 3-fold higher at the poles than at the equator. Conductance was about 59% higher over the air cell than over the chorioallantoic part of the egg. Surface-specific perfusion was 12% higher in the air cell. Therefore the in the air cell was higher, and the lower, than values calculated for the whole egg. The mean difference in between the air cell and the chorioallantoic part of the egg was 14.8 Torr, and that of , was 7.0 Torr. These differences were somewhat dependent on total conductance. Respiratory gas exchange ratio ( ) was higher in the air cell (R=0.82) and lower in the chorioallantoic region (R=0.67) than for the whole egg (R=0.70). Air cell R increased slightly in eggs of higher total conductance.Mismatching of regional shell conductance and chorioallantoic perfusion contributes to a functional venous shunt that is partly responsible for nonequilibrium between the air cell and the blood in the chorioallantoic veins.Symbols and abbreviations D gas diffusity - F _A fractional surface area - F _G fractional conductance - G conductance - G _diff diffusion conductance - G _perf perfusion conductance - PA average gas pressure (O₂ or CO₂) - Pac gas pressure in air cell - PE gas pressure in respiratory chamber - Pca gas pressure over chorioallantois - perfusion     

Purification and properties of a hyperthermoactive α-amylase from the archaeobacterium Pyrococcus woesei

The cultivation of the hyperthermophilic archaeobacterium Pyrococcus woesei on starch under continuous gassing (80% H₂:20% CO₂) caused the formation of 250 U/l of an extremely thermoactive and thermostable -amylase. In a complex medium without elemental sulphur under 80% N₂ and 20% CO₂ atmosphere enzyme production could be elevated up to 1000 U/l. Pyrococcus woesei grew preferentially on poly-and oligosaccharides. The amylolytic enzyme formation was constitutive. Enzyme production was also observed in continuous culture at dilution rates from 0.1 to 0.4 h^-1. A 20-fold enrichment of -amylase was achieved after adsorption of the enzyme onto starch and its desorption by preparative gel electrophoresis. The -amylase consisted of a single subunit with a molecular mass of 70 000 and was catalytically active at a temperature range between 40°C and 130°C. Enzymatic activity was detected even after autoclaving at a pressure of 2 bars at 120°C for 5 h. The purified enzyme hydrolyzed exclusively -1,4-glycosidic linkages present in glucose polymers of various sizes. Unlike many -amylases from anaerobes the enzyme from P. woesei was unable to attack short chain oligosaccharides with a chain length between 2 and 6 glucose units.     

Effects of Barometric Pressure and Abnormal Gas Mixtures on Gaseous Exchange by the Avian Embryo

Gas moves through the pores of the egg shell by diffusion inthe gas phase. The gas flux is therefore determined by the productof the effective conductance of the shell and the partial pressuregradient of the gas between the ambient air and the inner sideof the shell. The partial pressure gradient of oxygen is decreasedby a reduction of the oxygen partial pressure in the ambientair. This can be achieved by reducing barometric pressure atnormal ambient oxygen concentration or by reducing ambient oxygenconcentration at standard barometric pressure. Both methodsare reported to decrease oxygen consumption of the embryo butto a different degree. At the same ambient oxygen pressure thereduction is less in eggs exposed to a reduced barometric pressure.In an attempt to explain this difference, chicken embryos aged16–19 days were exposed to various oxygen concentrationsand carbon dioxide production was measured. At subnormal oxygenconcentrations carbon dioxide output diminished as the oxygenconcentration was lowered and the duration of exposure was prolonged.At oxygen concentrations above normal a small but significantincrease in carbon dioxide production was found. Finally theresults are compared with those in the literature on the diverseeffects of a continuous reduction of barometric pressure andambient oxygen concentration. This difference is ascribed tothe fact that a reduction of barometric pressure not only decreasesoxygen partial pressure in the ambient air but also increaseseffective conductance of the egg shell, the latter being inverselyproportional to the barometric pressure.     

Altitudinal changes in temperature responses of net photosynthesis and dark respiration in tropical bryophytes

Background and Aims

There is a conspicuous increase of poikilohydric organisms (mosses, liverworts and macrolichens) with altitude in the tropics. This study addresses the hypothesis that the lack of bryophytes in the lowlands is due to high-temperature effects on the carbon balance. In particular, it is tested experimentally whether temperature responses of CO₂-exchange rates would lead to higher respiratory carbon losses at night, relative to potential daily gains, in lowland compared with lower montane forests.

Methods

Gas-exchange measurements were used to determine water-, light-, CO₂- and temperature-response curves of net photosynthesis and dark respiration of 18 tropical bryophyte species from three altitudes (sea level, 500 m and 1200 m) in Panama.

Key Results

Optimum temperatures of net photosynthesis were closely related to mean temperatures in the habitats in which the species grew at the different altitudes. The ratio of dark respiration to net photosynthesis at mean ambient night and day temperatures did not, as expected, decrease with altitude. Water-, light- and CO₂-responses varied between species but not systematically with altitude.

Conclusions

Drivers other than temperature-dependent metabolic rates must be more important in explaining the altitudinal gradient in bryophyte abundance. This does not discard near-zero carbon balances as a major problem for lowland species, but the main effect of temperature probably lies in increasing evaporation rates, thus restricting the time available for photosynthetic carbon gain, rather than in increasing nightly respiration rates. Since optimum temperatures for photosynthesis were so fine tuned to habitat temperatures we analysed published temperature responses of bryophyte species worldwide and found the same pattern on the large scale as we found along the tropical mountain slope we studied.     

Simultaneous gas exchange and fluorescence measurements indicate differences in the response of sunflower,bean and maize to water stress

Gas exchange and fluorescence measurements of attached leaves of water stressed bean, sunflower and maize plants were carried out at two light intensities (250 mol quanta m^-2s^-1 and 850 mol quanta m^-2s^-1). Besides the restriction of transpiration and CO₂ uptake, the dissipation of excess light energy was clearly reflected in the light and dark reactions of photosynthesis under stress conditions. Bean and maize plants preferentially use non-photochemical quenching for light energy dissipation. In sunflower plants, excess light energy gave rise to photochemical quenching. Autoradiography of leaves after photosynthesis in ¹⁴CO₂ demonstrated the occurrence of leaf patchiness in sunflower and maize but not in bean. The contribution of CO₂ recycling within the leaves to energy dissipation was investigated by studies in 2.5% oxygen to suppress photorespiration. The participation of different energy dissipating mechanisms to quanta comsumption on agriculturally relevant species is discussed.Abbreviations F_o minimal fluorescence - F_m maximal fluorescence - F_p peak fluorescence - g leaf conductance - P_N net CO₂ uptake - q_N coefficient of non-photochemical quenching - q_P coefficient of photochemical quenching     

<Emphasis Type="Italic">Lotus corniculatus</Emphasis> L. response to carbon dioxide concentration and radiation level variations

Carbon dioxide concentration and light conditions may greatly vary between mountainous and lowland areas determining the photosynthetic performance of plants species. This paper aimed to evaluate the photosynthetic responses of Lotus corniculatus, growing in a mountain and a lowland grassland, under low and high radiation and CO₂ concentration. Net photosynthetic rate, stomatal conductance, transpiration rate, and intercellular CO₂ concentration were measured while the water-use efficiency and the ratio of variable to maximal fluorescence were calculated. Photosynthetic response curves to different levels of radiation and intercellular CO₂ partial pressure were estimated. Our results showed that high radiation and CO₂ concentration enhanced water-use efficiency of plants at both sites, enabling them to use more efficiently the available water reserves under drought conditions. The increase of radiation and CO₂ concentration would enhance the photosynthetic performance of the mountainous population of L. corniculatus, which overall seems to express higher phenotypic plasticity.     

Simultaneous and independent effects of abscisic acid on stomata and the photosynthetic apparatus in whole leaves

(±)-Abscisic acid (ABA) at 10^-5 M was added to the transpiration stream of leaves of 16 species (C₃ and C₄, monocotyledons and dicotyledons). Stomatal responses followed one of three patterns: i) stomata that were wide and insensitive to CO₂ initially, closed partially and became sensitive to CO₂; ii) for stomata that were sensitive to CO₂ before the application of ABA, the range of highest sensitivity to CO₂ shifted from high to low intercellular partial pressures of CO₂, for instance in leaves of Zea mays from 170–350 to 70–140 bar; iii) when stomata responded strongly to ABA, their conductance was reduced to a small fraction of the initial conductance, and sensitivity to CO₂ was lost. The photosynthetic apparatus was affected by applications of ABA to various degrees, from no response at all (in agreement with several previous reports on the absence of effects of ABA on photosynthesis) through a temporary decrease of its activity to a lasting reduction. Saturation curves of photosynthesis with respect to the partial pressure of CO₂ in the intercellular spaces indicated that application of ABA could produce three phenomena: i) a reduction of the initial slope of the saturation curve (which indicates a diminished carboxylation efficiency); ii) a reduction of the level of the CO₂-saturated rate of assimilation (which indicates a reduction of the ribulose-1,5-bisphosphate regeneration capacity); and iii) an increase of the CO₂ compensation point. Photosynthesis of isolated mesophyll cells was not affected by ABA treatments. Responses of the stomatal and photosynthetic apparatus were usually synchronous and often proportional to each other, with the result that the partial pressure of CO₂ in the intercellular spaces frequently remained constant in spite of large changes in conductance and assimilation rate. Guard cells and the photosynthetic apparatus were able to recover from effects of ABA applications while the ABA supply continued. Recovery was usually partial, in the case of the photosynthetic apparatus occasionally complete. Abscisic acid did not cause stomatal closure or decreases in the rate of photosynthesis when it was applied during a phase of stomatal opening and induction of photosynthesis that followed a transition from darkness to light.Abbreviations and symbols A rate of CO₂ assimilation - ABA (±)-abscisic acid - c _a partial pressure of CO₂ in the ambient air or in the gas supplied to the leaf chambers - c _i partial pressure of CO₂ in the intercellular spaces of a leaf - e _a partial pressure of H₂O in the air - g conductance for water vapor - J quantum flux - T ₁ leaf temperature     

Adaptation of the Avian Egg to High Altitude

Theoretical predictions and experiments on eggs of domesticatedbirds indicate that the diffusion coefficient of gases is inverselyproportional to barometric pressure. Therefore potentially lethallosses of CO₂ and water vapor from eggs laid at high altitudemight result if the increased tendency of gases to diffuse atreduced barometric pressure were not counteracted in some manner.Limited data from two wild populations indicate that water lossfrom eggs is independent of altitude over a 3000 m elevationalgradient. Four different possibilities are discussed by whichcompensation for increased diffusion of water vapor might beachieved at high elevations 1) a reduction in eggshell conductance(GH₂O) 2) an increase in the initial water content of the eggs3) an increase in shell thickness, and 4) alteration of watervapor pressure in the nest microenvironment or incubation temperatureby variation in parental behavior. Mean GH₂O of eggs of twoprecocial and four altricial species breeding above 2800 m issignificantly reduced below values of related birds breedingat lower elevations, but no change in initial water contentor shell thickness has been observed in such eggs. Observationsof parental behavior in species breeding over wide elevationalgradients have not yet been made. Identification of the mechanismsby which eggshell structure is modified to achieve a reducedGH₂O the environmental cues used by females to determine theelevation of the breeding location and the rapidity with whichshell structuie can be modified awaits further research.     

Embryonic heart rate and oxygen pulse in two procellariiform seabirds,Diomedea immutabilis and Puffinus pacificus

Developmental patterns of embryonic heart rate were measured non-invasively in two procellariiform seabirds, the Laysan albatross (Diomedea immutabilis) and wedge-tailed shearwater (Puffinus pacificus), during prepipping and after pipping. The O₂ pulse, defined as the O₂ consumption per single heart beat, was calculated using the previously reported O₂ consumption for these species. The embryonic heart rate of the albatross was not changed by internal pipping (initial pipping event in this species), remained unchanged during the prolonged internal pipping period and tended to increase, although insignificantly, with the initiation of external pipping (second pipping event). Heart rate in the shearwater remained unchanged during the late prepipping stages, did not change with external pipping (initial pipping event), but increased during the prolonged internal pipping period (second pipping event) and reached a maximum on the last day of incubation. The developmental pattern of heart rate in the shearwater was very similar to that reported previously for the brown noddy, a member of the order Charadriiformes but with the same pipping sequence. Developmental patterns of embryonic O₂ pulse were also different between the two procellariiform seabirds. However, those of the shearwater and the noddy were similar. The sequence of access to atmospheric O₂ during development and hatching may be an important factor determining the developmental patterns of embryonic heart rate and O₂ pulse.Abbreviations A-VO₂ difference, arteriovenous oxygen difference - BCG ballistocardiogram of egg - CV coefficient of variation - EP external pipping - HR heart rate - IP internal pipping - mass mass of freshly laid egg - SD standard deviation     

Carbon fixation in eucalypts in the field

Summary The rate of CO₂ assimilation at light saturation and an intercellular CO₂ concentration of 350 l l^-1 (photosynthetic capacity), measured in leaves of Eucalyptus pauciflora, E. behriana, E. delegatensis and Acacia melanoxylon, declined over the course of cloudless days under naturally varying environmental conditions as well as under constant optimal conditions for high CO₂ uptake. Since the capacity did not recover during the light period, it was different from the midday depression of gas exchange. The change appeared to be caused neither by the diurnal variation of total leaf water potential, by photoinhibition of redox-reaction centres in photosystems nor by changes in the intrinsic properties of Ribulose-bisphosphate carboxylase-oxygenase. The decline was more pronounced in winter than in summer. It was related to the duration of illumination or the cumulative carbon gain. It was reversible in the following dark phase, and it did not occur on changeable days with short peaks of high light.Despite the decline in photosynthetic capacity, the initial slope of the CO₂ response of net photosynthesis, as obtained at low intercellular CO₂ concentrations, remained constant during the day, but declined at night when photosynthetic capacity recovered. In all cases stomatal conductance varied in parallel with photosynthetic capacity. The relevance of changes in photosynthetic capacity for the intercellular CO₂ concentration is discussed.Abbreviations and symbols A CO₂ assimilation - ABA abscisic acid - A_c350 photosynthetic capacity at c_i=350l l^-1 - c_i intercellular CO₂ concentration - g leaf conductance to water vapour - I photon flux density (irradiance) - P air pressure - P_i inorganic phosphate - R_d net CO₂ release at _* - Rubisco Ribulose-bisphosphate carboxylase-oxygenase - RuBP Ribulose-bisphosphate - T leaf temperature - w leaf-to-air water vapour concentration difference - A/c_i carboxylation efficiency at low c_i - _* light-independent CO₂ compensation point - total leaf water potential     

Photosynthesis,water use and growth of a C4 grass stand at high CO2 concentration

Leaf photosynthesis rate of the C₄ species Paspalum plicatulum Michx was virtually CO₂-saturated at normal atmospheric CO₂ concentration but transpiration decreased as CO₂ was increased above normal concentrations thereby increasing transpiration efficiency. To test whether this leaf response led growth to be CO₂-sensitive when water supply was restricted, plants were grown in sealed pots of soil as miniature swards. Water was supplied either daily to maintain a constant water table, or at three growth restricting levels on a 5-day drying cycle. Plants were either in a cabinet with normal air (340 mol (CO₂) mol^-1 (air)) or with 250 mol mol^-1 enrichment. Harvesting was by several cycles of defoliation.With abundant water supply high CO₂ concentration did not cause increased growth, but it did not cause an increase in growth over a wide range of growth-limiting water supplies either. Only when water supply was less than 30–50% of the amount used by the stand with a water-table was there evidence that dry weight growth was enhanced by high CO₂. In addition, with successive regrowth, the enhancing effect under a regime of minimal water allocations, became attenuated. Examination of leaf gas exchange, growth and water use data showed that in the long term stomatal conductance responses were of little significance in matching plant water use to low water allocation; regulation of leaf area was the mechanism through which consumption matched supply. Since high CO₂ effects operate principally via stomatal conductance in C₄ species, we postulate that for this species higher CO₂ concentrations expected globally in future will not have much effect on long term growth.     

Seasonal trends in leaf photosynthesis and stomatal conductance of drought stressed and nonstressed pearl millet as associated to vapor pressure deficit

Single leaf photosynthesis (Pn) and stomatal conductance (Cg) of drought stressed and nonstressed pearl millet [Pennisetum americanum (L.) Leeke] were measured across growth stages to determine if a pattern exists in Pn and Cg during the growing season and to evaluate the influence of air vapor pressure deficit (VPD_a) on the seasonal variations of Pn and Cg. Leaf photosynthesis and Cg were measured independently on pearl millet plants grown at the driest (drought stressed) and wettest (nonstressed) ends of a line-source irrigation gradient system. Well defined and predictable variations in both Pn and Cg were found across two growing seasons. Leaf photosynthesis of the nonstressed plants declined from a maximumof 25.8 mol m^–2 s^–1 at the flag leaf emergence (48 days after planting, DAP) to a minimum of 14.5 mol m^–2 s^–1 at physiological maturity. Stomatal conductance of the nonstressed plants peaked at the flowering and early grain fill stages and declined as plants approached maturity. In contrast, Pn and Cg of the stressed plants declined from a maximum at flag leaf emergence to a minimum at flowering and increased as plants approached maturity. High VPD_a during the flowering and grain fill stages induced stomatal closure and decreased Pn in the stressed plants. High mid-season VPD_a did not induce stomatal closure and did not reduce leaf photosynthesis in nonstressed plants. The lack of sensitivity of Pn to VPD_a in the nonstressed treatment suggests large air VPD such as that prevalent in southern Arizona does not limit the growth of irrigated pearl millet by limiting CO₂ assimilation.Abbreviations Cg stomatal conductance - DAP days after planting - Pn leaf photosynthesis - VPD_a air vapor pressure deficit - VPD_1-a leaf to air vapor pressure deficit Contribution of the Arizona Agricultural Experimental Station. Research supported in part by INTSORMIL/USAID.