Carbon dioxide exchange of developing avocado (Persea americana Mill.) fruit

Net efflux of CO(2) from attached avocado (Persea americana Mill.) fruit was measured periodically from three weeks after anthesis to fruit maturity. Net CO(2) exchange was determined in daylight (light respiration, R(l)) at a photosynthetic photon flux (PPF) greater than 600 micromol m(-1) s(-1), and in the dark (dark respiration, R(d)). Dark respiration and R(l) were highest during the early cell division stage of fruit growth (about 25 and 22 nmol CO(2) g(dw) (-1) s(-1), respectively) and decreased gradually until fruit maturity to about 1 and 0.5 nmol CO(2) nmol CO(2) g(dw) (-1) s(-1), respectively. Fruit photosynthesis, calculated from the difference between R(d) and R(l), ranged from 0.5 to 3.1 nmol CO(2) g(dw) (-1) s(-1). Net rate of CO(2) assimilation on a fruit dry weight basis was highest during the early stages of fruit growth and reached the lowest rate at fruit maturity. Net rate of CO(2) assimilation of fruit exposed to light was 0.4 to 2.5% of that for fully expanded leaves. Although the relative amount of carbon assimilated by the fruit was small compared with the total amount of carbon assimilated by the leaves, the data indicate that avocado fruit contribute to their own carbon requirement by means of CO(2) assimilated in the light.     

Interspecific and environmentally induced variation in foliar dark respiration among eighteen southeastern deciduous tree species

We measured variations in leaf dark respiration rate (Rd) and leaf nitrogen (N) across species, canopy light environment, and elevation for 18 co-occurring deciduous hardwood species in the southern Appalachian mountains of western North Carolina. Our overall objective was to estimate leaf respiration rates under typical conditions and to determine how they varied within and among species. Mean dark respiration rate at 20 degrees C (Rd,mass, micromol CO2 per kg leaf dry mass per s) for all 18 species was 7.31 micromol per kg per s. Mean Rd,mass of individual species varied from 5.17 micromol per kg per s for Quercus coccinea Muenchh. to 8.25 micromol per kg per s for Liriodendron tulipifera L. Dark respiration rate varied by leaf canopy position and was higher in leaves collected from high-light environments. When expressed on an area basis, dark respiration rate (Rd,area, micromol CO2 per kg leaf dry area per s) showed a strong linear relationship with the predictor variables leaf nitrogen (Narea, g N per square m leaf area) and leaf structure (LMA, g leaf dry mass per square m leaf area) (r squared = 0.62). This covariance was largely a result of changes in leaf structure with canopy position; smaller thicker leaves occur at upper canopy positions in high-light environments. Mass-based expression of leaf nitrogen and dark respiration rate showed that nitrogen concentration (Nmass, mg N per g leaf dry mass) was only moderately predictive of variation in Rd,mass for all leaves pooled (r squared = 0.11), within species, or among species. We found distinct elevational trends, with both Rd,mass and Nmass higher in trees originating from high-elevation, cooler growth environments. Consideration of interspecies differences, vertical gradients in canopy light environment, and elevation, may improve our ability to scale leaf respiration to the canopy in forest process models.     

Stem growth and respiration in loblolly pine plantations differing in soil resource availability

Stem respiration and growth in 10-year-old loblolly pine (Pinus taeda L.) plantations were measured monthly during the third year of fertilization and irrigation treatments to determine whether soil resource availability differentially altered growth and respiration in stem tissue. Fertilized trees had significantly greater stem biomass, stem nitrogen concentration ([N]) and growth rate than unfertilized trees. Stem respiration (Rt) was significantly greater in fertilized trees when expressed on a per unit surface area (Rt,a, micromol CO2 m-2 s-1), sapwood volume (Rt,v, micromol CO2 m-3 s-1), or mass (Rt,w, nmol CO2 g-1 s-1) basis; however, there was no difference between treatments when expressed as a function of stem N content (Rt,n, micromol CO2 (mol N)-1 s-1). Irrigation had no significant effect on Rt or annual stem growth. Daily total respiration (Rd, mol CO2 m-2 day-1) and stem diameter growth both had a seasonal bimodal pattern with peaks in early spring and midsummer. Stem [N] declined significantly during the growing season. Stem growth rate and [N] explained 75% of the seasonal variation in temperature-normalized Rt,a. The mature tissue method was used to partition total stem respiration (Rt) into maintenance (Rm) and growth (Rg) components. There was a linear correlation between winter Rt,v, a measure of basal Rm, and sapwood N content; however, Rt,v per unit N was greater in January before diameter growth started than in the following December after growth ceased, indicating that Rt,v declined as stem diameter increased. Consequently, estimates of annual maintenance respiration (RM) based on January data were 44% higher than estimates based on December data. Growth respiration was correlated with stem growth rate (r2 = 0.55). The growth respiration coefficient (rg)-the slope of the relationship between Rg and stem growth rate-was 0.24. Respiration accounted for 37% of annual stem carbon budget. Stem carbon-use efficiency (CUE)-the ratio of stem growth to stem growth plus respiration-averaged 0.63 and was unaffected by fertilization.     

Exposure to elevated carbon dioxide concentration in the dark lowers the respiration quotient of Vitis cane wood

Cane cuttings of the grapevine rootstock Vitis rupestris Scheele x V. riparia Michx. cv. 3309 Couderc were brought out of endodormancy by warming at 30 degrees C. Cane pieces (12 to 13 cm long) with nodes containing a primary bud were placed in a gas exchange system and monitored for net respiratory fluxes of CO2 and O2. Grapevine respiration rates expressed on a wood volume basis were 1.4 to 3.4 mmol CO2 or O2 m-3s-1, which is higher than stem respiration rates reported for many other woody taxa but similar to rates measured for ecodormant buds of other Vitis species. Passive water loss from canes was 0.7 to 1.2 mmol H2O m-3s-1. During a 7-day period, nonstructural carbohydrate concentrations in cane wood declined only slightly, whereas sucrose was nearly completely consumed. When ambient CO2 concentration ([CO2]) was raised from 300 to 750 micro molmol-1 and then 2000 micromol mol-1, net CO2 exchange rates declined by 5.9 +/- 0.6 and then 11.0 +/- 0.6%, whereas net O2 consumption rates remained about constant. The mean respiration quotient (net CO2/O2 flux) for canes with intact ecodormant buds was 0.99 +/- 0.03 when the [CO2] was 300 micromol mol-1, and decreased to 0.87 +/- 0.03 and 0.088 +/- 0.02 when the [CO2] was increased to 750 and 2000 micromol mol-1, respectively. The results support the hypothesis that, in Vitis canes, inhibition of respiratory CO2 efflux in response to high [CO2] is an indirect consequence of non-photosynthetic carboxylation reactions, and not a result of inhibition of respiratory metabolism.     

Spatial distribution of leaf morphological and physiological characteristics in relation to local radiation regime within the canopies of 3-year-old Populus clones in coppice culture

Spatial distributions of leaf characteristics relevant to photosynthesis were compared within high-density coppice canopies of Populus spp. of contrasting genetic origin. We studied three clones representative of the range in growth potential, leaf morphology, coppice and canopy structure: Clone Hoogvorst (Hoo) (Populus trichocarpa Torr. & Gray x Populus deltoides Bartr. & Marsh), Clone Fritzi Pauley (Fri) (Populus trichocarpa Torr. & Gray) and Clone Wolterson (Wol) (Populus nigra L.). Leaf area index ranged from 2.7 (Fri and Wol) to 3.8 (Hoo). The clones exhibited large vertical variation in leaf area density (0.02-1.42 m2 m-3). Leaf dry mass per unit leaf area (DM(A)) increased with increasing light in Clones Hoo and Fri, from about 56 g m-2 at the bottom of the canopy to 162 g m-2 at the top. In Clone Wol, DM(A) varied only from 65 to 100 g m-2, with no consistent relationship with respect to light. Conversely, nitrogen concentration on a mass basis was nearly constant (around 1.3-2.1%) within the canopies of Clones Hoo and Fri, but increased strongly with light in Clone Wol, from 1.4% at the bottom of the canopy to 4.1% at the top. As a result, nitrogen per unit leaf area (N(A)) increased with light in the canopies of all clones, from 0.9 g m-2 at the bottom to 2.9 g m-2 at the top. Although a single linear relationship described the dependence of maximum carboxylation rate (17-93 micromol CO2 m-2 s-1) or electron transport capacity (45-186 micromol electrons m-2 s-1) on N(A), for all clones, Clone Wol differed from Clones Hoo and Fri by exhibiting a higher dark respiration rate at low N(A) (1.8 versus 0.8 micromol CO2 m-2 s-1).     

Coarse and fine root respiration in aspen (Populus tremuloides)

Coarse and fine root respiration rates of aspen (Populus tremuloides Michx.) were measured at 5, 15 and 25 degrees C. Coarse roots ranged from 0.65 to 4.45 cm in diameter, whereas fine roots were less than 5 mm in diameter. To discriminate between maintenance and growth respiration, root respiration rates were measured during aboveground growing periods and dormant periods. An additional measurement of coarse root respiration was made during spring leaf flush, to evaluate the effect of mobilization of resources for leaf expansion on root respiration. Fine roots respired at much higher rates than coarse roots, with a mean rate at 15 degrees C of 1290 micromol CO2 m-3 s-1 during the growing period, and 660 micromol CO2 m-3 s-1 during the dormant period. The temperature response of fine root respiration rate was nonlinear: mean Q10 was 3.90 for measurements made at 5-15 degrees C and 2.19 for measurements made at 15-25 degrees C. Coarse root respiration rates measured at 15 degrees C in late fall (dormant season) were higher (370 micromol CO2 m-3 s-1) than rates from roots collected at leaf flush and early summer (200 micromol CO2 m-3 s-1). The higher respiration rates in late fall, which were accompanied by decreased total nonstructural carbohydrate (TNC) concentrations, suggest that respiration rates in late fall included growth expenditures, reflecting recent radial growth. Neither bud flush nor shoot growth of the trees caused an increase in coarse root respiration or a decrease in TNC concentrations, suggesting a limited role of coarse roots as reserve storage organs for spring shoot growth, and a lack of synchronization between above- and belowground growth. Pooling the data from the coarse and fine roots showed a positive correlation between nitrogen concentration and respiration rate.     

Gas exchange characteristics of a Canarian laurel forest tree species (Laurus azorica) in relation to environmental conditions and leaf canopy position

Diurnal courses of gas exchange were measured over a 1-year period in fully expanded current-year leaves in the upper (sun-exposed, 18 m above ground) and the lower (shaded, 12 m above ground) canopy of Laurus azorica (Seub.) Franco, a major canopy species of the Canarian laurel forest in Tenerife, Canary Islands, Spain. Laurus azorica exhibited high leaf plasticity in gas exchange characteristics, with a maximum carbon assimilation rate (Amax) of shade leaves about 50% that of sun leaves. This difference reflects the high leaf area index (LAI) of the stand and the correspondingly sharp light attenuation with increasing canopy depth. In sun leaves, Amax peaked at about 11 micromol m-2 s-1 and maximum transpiration (E) was about 8 mmol m-2 s-1, which corresponded with a maximum stomatal conductance (gs) of about 650 mmol m-2 s-1. Mean maximum instantaneous water-use efficiency (WUE) was 1.5 mmol mol-1 and the mean maximum A/gs was 20-35 micromol mol-1. Mean minimum internal CO2 concentration (Ci) was 225 micromol mol-1. Although high air vapor pressure deficit (VPD) caused a small decrease in gs, it remained high enough to maintain relatively high A and E. These gas exchange characteristics indicate a non-conservative use of water, which is appropriate for a species subject to droughts that are mild or of short duration. In this respect, Laurus azorica differs from its congener, L. nobilis L., of the Mediterranean region and other shrubs growing in Mediterranean-type climates in California and Chile that have to withstand more severe or more prolonged droughts.     

Effects of light availability on leaf gas exchange and expansion in lychee (Litchi chinensis)

Effects of photosynthetic photon flux density (PPFD) on leaf gas exchange of lychee (Litchi chinensis Sonn.) were studied in field-grown "Kwai May Pink" and "Salathiel" orchard trees and young potted "Kwai May Pink" plants during summer in subtropical Queensland (27 degrees S). Variations in PPFD were achieved by shading the trees or plants 1 h before measurement at 0800 h. In a second experiment, potted seedlings of "Kwai May Pink" were grown in a heated greenhouse in 20% of full sun (equivalent to maximum noon PPFD of 200 micromol m(-2)xs(-1)) and their growth over three flush cycles was compared with seedlings grown in full sun (1080 micromol m(-2)xs(-1)). Young potted plants of "Kwai May Pink" were also grown outdoors in artificial shade that provided 20, 40, 70 or 100% of full sun (equivalent to maximum PPFDs of 500, 900, 1400 and 2000 micromol m(-2)xs(-1)) and measured for shoot extension and leaf area development over one flush cycle. Net CO2 assimilation increased asymptotically in response to increasing PPFD in both orchard trees and young potted plants. Maximum rates of CO2 assimilation (11.9 +/- 0.5 versus 6.3 +/- 0.2 micromol CO2 m(-2) s(-1)), dark respiration (1.7 +/- 0.3 versus 0.6 +/- 0.2 micromol CO2 m(-2) s(-1)), quantum yield (0.042 +/- 0.005 versus 0.027 +/- 0.003 mol CO2 mol(-1)) and light saturation point (1155 versus 959 micromol m(-2) s(-1)) were higher in orchard trees than in young potted plants. In potted seedlings grown in a heated greenhouse, shoots and leaves exposed to full sun expanded in a sigmoidal pattern to 69 +/- 12 mm and 497 +/- 105 cm(2) for each flush, compared with 27 +/- 7 mm and 189 +/- 88 cm(2) in shaded seedlings. Shaded seedlings were smaller and had higher shoot:root ratios (3.7 versus 3.1) than seedlings grown in full sun. In the potted plants grown outdoors in 20, 40, 70 or 100% of full sun, final leaf area per shoot was 44 +/- 1, 143 +/- 3, 251 +/- 7 and 362 +/- 8 cm(2), respectively. Shoots were also shorter in plants grown in shade than in plants grown in full sun (66 +/- 5 mm versus 101 +/- 2 mm). Photosynthesis in individual leaves of lychee appeared to be saturated at about half full sun, whereas maximum leaf expansion occurred at higher PPFDs. We conclude that lychee plants can persist as seedlings on the forest floor, but require high PPFDs for optimum growth.     

Carbohydrate requirements of peach fruit growth and respiration

Data on the seasonal patterns of fruit growth and dark respiration of two peach (Prunus persica (L.) Batsch) cultivars were combined with temperature data to calculate the carbohydrate requirements of an "average" peach fruit from bloom to harvest. The two peach cultivars used were June Lady (an early maturing (mid-June) cultivar) and O'Henry (a late maturing (early-August) cultivar). At harvest, the mean dry weight of the June Lady fruit was 17.8 g (139.7 g fresh weight) and of O'Henry fruits was 30.9 g (213.9 g fresh weight), and the times from full bloom to harvest were 107 and 154 days, respectively. The total calculated fruit respiration requirements were 132 and 300 mmol CO(2) fruit(-1) season(-1) for June Lady and O'Henry fruits, respectively. Total calculated carbohydrate requirements for fruit growth and respiration are 23.9 and 43.8 g CH(2)O fruit(-1) season(-1) for June Lady and O'Henry fruits, respectively. Fruit respiration accounted for 16.3% of the total carbohydrate requirements of June Lady fruits and 0.5% of the total carbohydrate requirements of O'Henry fruits.     

Moderate shade can increase net gas exchange and reduce photoinhibition in citrus leaves

Daily variations in net gas exchange, chlorophyll a fluorescence and water relations of mature, sun-acclimated grapefruit (Citrus paradisi Macfady.) and orange (Citrus sinensis L. Osbeck) leaves were determined in tree canopies either shaded with 50% shade screens or left unshaded (sunlit). Mean daily maximum photosynthetic photon flux density (PPFD) under shade varied from 500 to 700 micromol m-2 s-1 and was sufficient to achieve maximum net CO2 assimilation rates (A CO2). Responses of grapefruit and orange leaves to shading were remarkably similar. At midday, on bright clear days, the temperatures of sunlit leaves were 2-6 degrees C above air temperature and 1-4 degrees C above the temperatures of shaded leaves. Although midday depressions of stomatal conductance (gs) and A CO2 were observed in both sunlit and shaded leaves, shaded leaves had lower leaf-to-air vapor pressure differences (D) along with higher gs, A CO2 and leaf water-use efficiency than sunlit leaves. Estimated stomatal limitation to A CO2 was generally less than 25% and did not differ between shaded and sunlit leaves. Leaf intercellular CO2 partial pressure was not altered by shade treatment and did not change substantially with increasing D. Radiation and high temperature stress-induced non-stomatal limitation to A CO2 in sunlit leaves was greater than 40%. Reversible photoinhibition of photosystem II efficiency was more pronounced in sunlit than in shaded leaves. Thus, non-stomatal factors play a major role in regulating A CO2 of citrus leaves during radiation and high temperature stress.     

Daily time course of whole-shoot gas exchange rates in two drought-exposed Mediterranean shrubs

Effects of drought on water relations, whole-shoot gas-exchange characteristics, and pigment and zeatin concentrations were investigated in the Mediterranean shrubs rosemary (Rosmarinus officinalis L.) and lavender (Lavandula stoechas L.). Two-year-old, greenhouse-grown plants were placed in a whole-shoot gas-exchange measurement system and subjected to 10 days of drought, resulting in severe water stress, and then re-watered for 5 days in order to study their recovery. Water stress resulted in a significant decline in maximum whole-shoot net CO2 assimilation rates (An) for both species that was associated with reductions in leaf area and stomatal conductance. Because shoot dark respiration rate (Rd) was less sensitive to water stress than An, shoot Rd/An ratio increased from about 15 to 95% during water stress. No major changes in chlorophyll and carotenoid concentrations of rosemary leaves were observed during the experiments, but chlorophyll and carotenoid concentrations fell significantly in water-stressed lavender leaves. Zeatin concentrations were higher in rosemary leaves than in lavender leaves during water stress. After re-watering, whole-shoot An and Rd rapidly recovered to their pre-drought rates.     

不同桉树人工林土壤呼吸旱雨季变化特征

以雷州半岛气候背景条件下具有良好培育前景的5种桉树人工林(湿加松林为对照)为研究对象,测定并分析各个林分土壤呼吸速率在旱季和雨季的差异,以揭示其与土壤温、湿度的关系.结果表明:土壤呼吸速率在旱季表现为先减后增变化趋势,在雨季表现为先增后减或逐渐减小变化趋势,旱、雨季变化特征明显.6个林分旱、雨季土壤呼吸速率均值分别为1.63~3.32μmol·m-2·s-1和2.55~4.36μmol·m-2·s-1.旱季土壤温、湿度共同促进土壤呼吸作用,雨季土壤温度促进土壤呼吸,土壤湿度抑制土壤呼吸作用.     

Ecosystem respiration in a young ponderosa pine plantation in the Sierra Nevada Mountains, California

We estimated total ecosystem respiration from a ponderosa pine (Pinus ponderosa Dougl. ex Laws.) plantation in the Sierra Nevada Mountains near Georgetown, California, from June to October, 1998. We apportioned ecosystem respiration among heterotrophic, root, stem and foliage based on relationships for each component that considered microclimate and vegetation characteristics. We measured each respiration component at selected sampling points, and scaled the measurements up to the ecosystem based on modeled relationships. Over the study period, total mean ecosystem respiration was 5.7 +/- 1.3 mumol m-2 s-1 (based on daily mean), comprising about 67% from soil-surface CO2 efflux, 10% from stem and branch respiration and 23% from foliage respiration. Shrub leaves contributed about 24% to total foliage respiration, and current-year needles (1998 age class) accounted for 40% of total tree needle respiration. Root respiration accounted for 47% of soil-surface CO2 efflux. We conclude that ecosystem respiration can be estimated based on daily mean air and soil temperatures through exponential relationships with r2 values of 0.85 and 0.87, respectively. When based on both air and soil temperatures, about 91% of the variation in total ecosystem respiration could be explained by a linear regression.     

高寒冻土层地区不同土壤改良措施对花叶海棠光合特性的影响

为促进花叶海棠在天峻县的生长,采用不同比例的森林土、泥炭、腐熟羊粪、河砂和珍珠岩改良土壤,分析不同土壤改良措施下花叶海棠叶片的净光合速率、蒸腾速率、气孔导度及胞间CO_2浓度。结果表明:在6个处理中,S_3(50%森林土+10%泥炭+10%腐熟羊粪+5%河砂+5%珍珠岩+20%原土)、S_2(40%森林土+10%泥炭+10%腐熟羊粪+5%河砂+5%珍珠岩+30%原土)处理的叶片平均净光合速率较大,分别为14.11μmol m~(-2)s~(-1)、13.72μmol m~(-2)s~(-1),增长率分别为17.58%、14.32%;S_3、S_6(10%森林土+50%泥炭+10%腐熟羊粪+5%河砂+5%珍珠岩+20%原土)处理的叶片平均蒸腾速率较大,分别为12.44mol m~(-2)s~(-1)、11.64mol m~(-2)s~(-1),增长率分别为65.65%、54.99%;S_6、S_3处理的叶片平均气孔导度较大,分别为0.455mol m~(-2)s~(-1)、0.426mol m~(-2)s~(-1),增长率分别为49.18%、39.68%;S_3处理的叶片平均胞间CO_2浓度较大,为280.1μmol mol~(-1),增长率为21.10%;不同土壤改良措施与花叶海棠叶片的净光合速率、蒸腾速率及胞间CO_2浓度均呈极显著性相关(P0.01),与气孔导度呈显著相关(P0.05),经各项指标综合分析,筛选出经S_3处理的试验地最适宜花叶海棠生长。     

Interaction of nutrient limitation and elevated CO2 concentration on carbon assimilation of a tropical tree seedling (Cedrela odorata)

Carbon assimilation by Cedrela odorata L. (Meliaceae) seedlings was investigated in ambient and elevated CO2 concentrations ([CO2]) for 119 days, using small fumigation chambers. A solution containing macro- and micronutrients was supplied at two rates. The 5% rate (high rate) was designed to avoid nutrient limitation and allow a maximum rate of growth. The 1% rate (low rate) allowed examination of the effect of the nutrient limitation-elevated CO2 interaction on carbon assimilation. Root growth was stimulated by 23% in elevated [CO2] at a high rate of nutrient supply, but this did not lead to a change in the root:shoot ratio. Total biomass did not change at either rate of nutrient supply, despite an increase in relative growth rate at the low nutrient supply rate. Net assimilation rates and relative growth rates were stimulated by the high rate of nutrient addition, irrespective of [CO2]. We used a biochemical model of photosynthesis to investigate assimilation at the leaf level. Maximum rate of electron transport (Jmax) and maximum velocity of carboxylation (Vcmax) did not differ significantly with CO2 treatment, but showed a substantial reduction at the low rate of nutrient supply. Across both CO2 treatments, mean Jmax for seedlings grown at a high rate of nutrient supply was 75 micromol m(-2) s(-1) and mean Vcmax was 27 micromol m(-2) s(-1). The corresponding mean values for seedlings grown at a low rate of nutrient supply were 36 micromol m(-2) s(-1) and 15 micromol m(-2) s(-1), respectively. Concentrations of leaf nitrogen, on a mass basis, were significantly decreased by the low nutrient supply rate, in proportion to the observed decrease in photosynthetic parameters. Chlorophyll and carbohydrate concentrations of leaves were unaffected by growth [CO2]. Because there was no net increase in growth in response to elevated [CO2], despite increased assimilation of carbon at the leaf level, we hypothesize that the rate of respiration of non-photosynthetic organs was increased.     

潮间带消浪林海滨木槿光合作用的初步研究

以慈溪杭州湾滨海绿地试验林场的海滨木槿为对照,对比分析了杭州湾南岸潮间带消浪林海滨木槿的光合作用日变化、光合作用光响应曲线以及叶绿素含量特征。结果表明,消浪林海滨木槿净光合速率Pn日变化与对照相同,均呈双峰曲线,但其平均值显著下降,仅为对照的76.02%;光响应曲线经非直角双曲线拟合得到,潮间带海滨木槿最大净光合速率Amax为(22.36±3.22)μmol.m-2.s-1,是对照的91.75%,而光补偿点LCP为(28.57±1.51)μmol.m-2.s-1和暗呼吸速率Rd(1.98±0.31)μmol.m-2.s-1却是对照的1.44倍和1.33倍,表观量子效率AQ Y与对照相差不大;消浪林海滨木槿叶绿素a、叶绿素b和叶绿素总含量分别为(0.82±0.04)g.kg-1(、0.12±0.00)g.kg-1和(0.94±0.04)g.kg-1,分别是对照的65.08%、100.00%和68.12%。方差分析结果表明,消浪林海滨木槿的Pn、Amax、LCP、Rd、叶绿素a含量、叶绿素总含量与对照间存在显著差异,其他指标差异不显著。     

Shoot development,chlorophyll, gas exchange and carbohydrates in lychee seedlings (Litchi chinensis)

Shoot growth, chlorophyll concentrations, gas exchange and starch concentrations were studied in lychee (Litchi chinensis Sonn.) seedlings of cultivar "Wai Chee" grown in a heated greenhouse at Nambour in subtropical Australia (27 degrees S). We also examined the effects of shoot defoliation and root pruning on leaf expansion. Shoot growth showed a rhythmic cycle under constant greenhouse conditions, with a mean duration of flushing of 20 days and an interval of 10 days over three cycles. Shoots and leaves expanded in a sigmoidal pattern to about 80 mm and 500 cm(2), respectively, for each flush. Starch concentrations of the lower stem and roots decreased as the young red leaves expanded, and increased as the fully expanded leaves turned dark green. Chlorophyll concentrations and net CO(2) assimilation rate were highest in the fully expanded dark green leaves. Removing 50% of the area of each fully expanded leaf had little effect on the expansion of younger leaves, but total biomass of defoliated plants was only 60% of that of controls. In contrast, removing half the roots just before bud swelling reduced final leaf area by 80%. We conclude that the young shoot has relatively low rates of photoassimilation until the leaves are fully expanded and dark green, and depends on assimilates from elsewhere in the plant. During leaf expansion, translocation of assimilates to the shoot occurred at the expense of the roots.     

Leaf chlorophyll,net gas exchange and chloroplast ultrastructure in citrus leaves of different nitrogen status

One-year-old 'Cleopatra mandarin' (Citrus reticulata Blanco) seedlings were raised in a greenhouse and fertilized with nitrogen (N) at four application frequencies. Nitrogen-deficient leaves (86 mmol N m-2) had less chlorophyll per unit area, but a greater chlorophyll a:b ratio than N-fertilized leaves (> 187 mmol N m-2). Leaf dry mass per area (DM area-1) and total chlorophyll concentration increased linearly with increasing leaf N, whereas chlorophyll a:b ratio declined. Net assimilation of CO2 (A(CO2)) and leaf water-use efficiency (WUE) reached maximum values in leaves with approximately 187 mmol N m-2. Nitrogen-deficient leaves exhibited small chloroplasts with no starch granules; grana and stroma lamellae that coincided with the accretion of numerous large plastoglobuli in the stroma disintegrated. High-N leaves had large chloroplasts with well-developed grana, stroma lamellae and starch granules that enlarged with increasing N concentration. The lack of an increase in A(CO2) capacity at leaf N concentrations above 187 mmol N m-2 appeared to be correlated with the presence of numerous large starch granules.     

Seasonal trends in photosynthetic parameters and stomatal conductance of blue oak (Quercus douglasii) under prolonged summer drought and high temperature

Understanding seasonal changes in photosynthetic parameters and stomatal conductance is crucial for modeling long-term carbon uptake and energy fluxes of ecosystems. Gas exchange measurements of CO2 and light response curves on blue oak leaves (Quercus douglasii H. & A.) were conducted weekly throughout the growing season to study the seasonality of photosynthetic capacity (Vcmax) and Ball-Berry slope (m) under prolonged summer drought and high temperature. A leaf photosynthetic model was used to determine Vcmax. There was a pronounced seasonal pattern in Vcmax. The maximum value of Vcmax, 127 micromol m(-2) s(-1), was reached shortly after leaf expansion in early summer, when air temperature was moderate and soil water availability was high. Thereafter, Vcmax declined as the soil water profile became depleted and the trees experienced extreme air temperatures, exceeding 40 degrees C. The decline in Vcmax was gradual in midsummer, however, despite extremely low predawn leaf water potentials (Psipd, approximately -4.0 MPa). Overall, temporal changes in Vcmax were well correlated with changes in leaf nitrogen content. During spring leaf development, high rates of leaf dark respiration (Rd, 5-6 micromol m(-2) s(-1)) were observed. Once a leaf reached maturity, Rd remained low, around 0.5 micromol m(-2) s(-1). In contrast to the strong seasonality of Vcmax, m and marginal water cost per unit carbon gain (partial partial differential E/ partial partial differential A) were relatively constant over the season, even when leaf Psipd dropped to -6.8 MPa. The constancy of partial partial differential E/ partial partial differential A suggests that stomata behaved optimally under severe water-stress conditions. We discuss the implications of our findings in the context of modeling carbon and water vapor exchange between ecosystems and the atmosphere.     

14C Allocation in tree-soil systems

We studied whole-tree C allocation with special emphasis on the quantification of C allocation to roots and root respiration. To document seasonal patterns of C allocation, 2-year-old hybrid poplar trees greater than 3 m tall were labeled with (14)CO(2) in a large Plexiglas chamber in the field, in July and September. Climate and CO(2) concentration were controlled to track ambient conditions during labeling. Individual tree canopy CO(2) assimilation averaged 3.8 micromol CO(2) m(-2) s(-1) (12.9 g C day(-1) tree(-1)) in July and 6.2 micromol CO(2) m(-2) s(-1) (9.8 g C day(-1) tree(-1)) in September. Aboveground dark respiration was 12% of net daytime C fixation in July and 15% in September. Specific activity of root-soil respiration peaked 2 days after labeling and stabilized to less than 5% of maximum 2 weeks later. Low specific activity of root-soil respiration and a labeled pool of root C demonstrated that current photosynthate was the primary source of C for root growth and maintenance during the growing season. Root respiration averaged 20% of total soil respiration in both July and September based on the proportion of labeled C respired to labeled C fixed. In July, 80% of the recovered (14)C was found above ground and closely resembled the weight distribution of the growing shoot. By September, 51% of the recovered (14)C was in the root system and closely resembled the weight distribution of different size classes of roots. The finding that the distribution of biomass and (14)C were similar verified that the C introduced during labeling followed normal seasonal translocation pathways. Results are compared to smaller scale labeling studies and the suitability of the approach for studying long-term C fluxes is discussed.