Photoprotective Effects of D1 Protein Turnover and the Lutein Cycle on Three Ephemeral Plants under Heat Stress

To clarify the characteristics of photoinhibition and the primary defense mechanisms of ephemeral plant leaves against photodestruction under high temperature stress, inhibitors and the technology to determine chlorophyll fluorescence were used to explore the protective effects of D1 protein turnover and the lutein cycle in the high temperature stress of the leaves of three ephemeral plants. The results showed that the maximum light conversion efficiency (Fv/Fm) of the ephemeral plant leaves decreased, and the initial fluorescence (Fo) increased under 35°C ± 1°C heat stress for 1–4 h or on sunny days in the summer. Both Fv/Fm and Fo could be recovered after 8 h of darkness or afternoon weakening of the external temperature. Streptomycin sulfate (SM) or dithiothreitol (DTT) accelerated the decrease of Fv/Fm and the photochemical quenching coefficient (qP) in the leaves of three ephemeral plants at high temperature, and the decrease was greater in the SM than in the DTT treatment. When the high temperature stress was prolonged, the Y(II) values of light energy distribution parameters of PSII decreased, and the Y(NPQ) and Y(NO) values increased gradually in all the treatment groups of the three ephemeral plants. The results showed that the leaves of the three ephemeral plants had their own highly advanced mechanisms to protect against photodamage, which inhibited the turnover of D1 protein and xanthophyll cycle. This can damage the PSII reaction center in the leaves of the three ephemeral plants under high temperature. The protective effect of D1 protein turnover on heat stress in Erodium oxyrrhynchum and Senecio subdentatus was greater than that of the lutein cycle, while the protective effect of lutein cycle was greater than that of D1 protein turnover in Heliotropium acutiflorum subjected to heat damage.     

Characterization of Chloroplasts Isolated from Triazine-Susceptible and Triazine-Resistant Biotypes of Brassica campestris L

Chloroplasts isolated from triazine-susceptible and triazine-resistant biotypes of Brassica campestris L. were analyzed for lipid composition, ultrastructure, and relative quantum requirements of photosynthesis. In general, phospholipids, but not glycolipids in chloroplasts from the triazine-resistant biotype had a higher linolenic acid concentration and lower levels of oleic and linoleic fatty acids, than chloroplasts from triazine-susceptible plants. Chloroplasts from the triazine-resistant biotype had a 1.6-fold higher concentration of t-Δ3-hexadecenoic acid with a concomitantly lower palmitic acid concentration in phosphatidylglycerol. Phosphatidylglycerol previously has been hypothesized to be a boundary lipid for photosystem II. Chloroplasts from the triazine-resistant biotype had a lower chlorophyll a/b ratio and exhibited increased grana stacking. Light-saturation curves revealed that the relative quantum requirement for whole chain electron transport at limiting light intensities was lower for the susceptible biotype than for the triazine-resistant biotype. Although the level of the chlorophyll a/b light-harvesting complex associated with photosystem II was greater in resistant biotypes, the increased levels of the light-harvesting complex did not increase the photosynthetic efficiency enough to overcome the rate limitation that is inherited concomitantly with the modification of the Striazine binding site.     

Tolerances of wild potato species from different altitudes to cold and heat

The ability of wild potatoes (Solanum spp.) to adapt to potentially stressful environmental temperatures was investigated by measuring the cold and heat tolerances of plants grown near sea-level in Lima following collection of tubers from plants growing naturally at altitudes ranging from 450 to 4,200 m. Relative cold tolerance was measured in leaves stored at 0°C by the decrease in the induced rise of chlorophyll fluorescence. Similarly, changes in chlorophyll fluorescence were used to determine the relative heat tolerance of leaves heated at 41°C for 10 min. With increasing altitude, the cold tolerance of different species tended to increase and conversely, heat tolerance decreased. However, these two genotypic adaptations were not closely correlated and appear to vary independently of each other in response to climate.     

Genotypic response of detached leaves versus intact plants for chlorophyll fluorescence parameters under high temperature stress in wheat

The genotypic response of wheat cultivars as affected by two methods of heat stress treatment (treatment of intact plants in growth chambers versus treatment of detached leaves in test tubes) in a temperature controlled water bath were compared to investigate how such different methods of heat treatment affect chlorophyll fluorescence parameters. A set of 41 spring wheat cultivars differing in their maximum photochemical efficiency of photosystem (PS) II (F_v/F_m) under heat stress conditions was used. These cultivars were previously evaluated based on the heat treatment of intact plants. The responses of the same cultivars to heat stress were compared between the two methods of heat treatment. The results showed that in detached leaves, all of the fluorescence parameters remained almost unaffected in control (20 °C at all durations tested), indicating that the detachment itself did not affect the fluorescence parameters. In contrast, heat induced reduction in the maximum photochemical efficiency of PSII of detached leaves occurred within 2 h at 40 °C and within 30 min at 45 °C, and the response was more pronounced than when intact plants were heat stressed for three days at 40 °C. The proportion of total variation that can be ascribed to the genetic differences among cultivars for a trait was estimated as genetic determination. During heat treatment, the genetic determination of most of the fluorescence parameters was lower in detached leaves than in intact plants. In addition, the correlation of the cultivar response in intact plants versus detached leaves was low (r = 0.13 (with expt.1) and 0.02 with expt.2). The most important difference between the two methods was the pronounced difference in time scale of reaction, which may indicate the involvement of different physiological mechanisms in response to high temperatures. Further, the results suggest that genetic factors associated with cultivar differences are different for the two methods of heat treatment.     

Similar Photosynthetic Performance in Low Light-Grown Isonuclear Triazine-Resistant and -Susceptible Brassica napus L

Triazine-resistant plants grown under moderate to high photon flux density (PFD) conditions exhibit decreased photon yield, decreased light-saturated O₂ evolution and slower growth than triazine-susceptible plants. In this study we tested the hypothesis that the comparable growth previously observed in resistant and susceptible Brassica napus L. lines grown under low PFD was accompanied by comparable photon yield and light-saturated O₂ evolution. We measured photon yield, O₂ flash yield, fluorescence decay kinetics, fluorescence transient kinetics, and quenching components, F_v/F_m and light saturated O₂ evolution in leaf disks of low PFD-grown triazine-resistant and susceptible B. napus isogenic lines. Results indicated that slow electron transfer from the primary to secondary quinone electron acceptors of photosystem II was still present in the resistant line but photon yield and light-saturated O₂ evolution were similar in the two B. napus lines. We conclude that the alteration in the D1 protein that confers resistance does not necessarily cause decreased photosynthetic performance. Decreased photon yield in resistant plants grown at high PFD is not a direct consequence of the alteration in D1, but represents secondary damage.     

Salinity treatment shows no effects on photosystem II photochemistry,but increases the resistance of photosystem II to heat stress in halophyte Suaeda salsa

Photosynthetic gas exchange, modulated chlorophyll fluorescence, rapid fluorescence induction kinetics, and the polyphasic fluorescence transients were used to evaluate PSII photochemistry in the halophyte Suaeda salsa exposed to a combination of high salinity (100-400 mM NaCl) and heat stress (35-47.5 degrees C, air temperature). CO(2) assimilation rate increased slightly with increasing salt concentration up to 300 mM NaCl and showed no decrease even at 400 mM NaCl. Salinity treatment showed neither effects on the maximal efficiency of PSII photochemistry (F(v)/F(m)), the rapid fluorescence induction kinetics, and the polyphasic fluorescence transients in dark-adapted leaves, nor effects on the efficiency of excitation energy capture by open PSII reaction centres (F(v)'/F(m)') and the actual PSII effciency (Phi(PSII)), photochemical quenching (q(P)), and non-photochemical quenching (q(N)) in light-adapted leaves. The results indicate that high salinity had no effects on PSII photochemistry either in a dark-adapted state or in a light-adapted state. With increasing temperature, CO(2) assimilation rate decreased significantly and no net CO(2) assimilation was observed at 47.5 degrees C. Salinity treatment had no effect on the response of CO(2) assimilation to high temperature when temperature was below 40 degrees C. At 45 degrees C, CO(2) assimilation rate in control plants decreased to zero, but the salt-adapted plants still maintained some CO(2) assimilation capacity. On the other hand, the responses of PSII photochemistry to heat stress was modified by salinity treatment. When temperature was above 35 degrees C, the declines in F(v)/F(m), Phi(PSII), F(v)'/F(m)', and q(P) were smaller in salt-adapted leaves compared to control leaves. This increased thermostability was independent of the degree of salinity, since no significant changes in the above-described fluorescence parameters were observed among the plants treated with different concentrations of NaCl. During heat stress, a very clear K step as a specific indicator of damage to the O(2)-evolving complex in the polyphasic fluorescence transients appeared in control plants, but did not get pronounced in salt-adapted plants. In addition, a greater increase in the ratio (F(i)-F(o))/(F(p)-F(o)) which is an expression of the proportion of the Q(B)-non-reducing PSII centres was observed in control plants rather than in salt-adapted plants. The results suggest that the increased thermostability of PSII seems to be associated with the increased resistance of the O(2)-evolving complex and the reaction centres of PSII to high temperature.     

Regulation of Photosynthesis in Triazine-Resistant and -Susceptible Brassica napus

The response of photosynthetic carbon assimilation and chlorophyll fluorescence quenching to changes in intercellular CO₂ partial pressure (C_i), O₂ partial pressure, and leaf temperature (15-35°C) in triazine-resistant and -susceptible biotypes of Brassica napus were examined to determine the effects of the changes in the resistant biotype on the overall process of photosynthesis in intact leaves. Three categories of photosynthetic regulation were observed. The first category of photosynthetic response, ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco)-limited photosynthesis, was observed at 15, 25, and 35°C leaf temperatures with low C_i. When the carbon assimilation rate was Rubisco-limited, there was little difference between the resistant and susceptible biotypes, and Rubisco activity parameters were similar between the two biotypes. A second category, called feedback-limited photosynthesis, was evident at 15 and 25°C above 300 microbars C_i. The third category, photosynthetic electron transport-limited photosynthesis, was evident at 25 and 35°C at moderate to high CO₂. At low temperature, when the response curves of carbon assimilation to C_i indicated little or no electron transport limitation, the carbon assimilation rate was similar in the resistant and susceptible biotypes. With increasing temperature, more electron transport-limited carbon assimilation was observed, and a greater difference between resistant and susceptible biotypes was observed. These observations reveal the increasing importance of photosynthetic electron transport in controlling the overall rate of photosynthesis in the resistant biotype as temperature increases. Photochemical quenching of chlorophyll fluorescence (q_P) in the resistant biotype never exceeded 60%, and triazine resistance effects were more evident when the susceptible biotype had greater than 60% q_P, but not when it had less than 60% q_P.     

Freezing injury in potato leaves

Time-temperature profiles of freezing leaves from frost-resistant (Solanum acaule Bitt.) and frost-susceptible (Solanum tuberosum L. subsp. tuberosum Hawkes) types of potatoes did not reveal any major differences. The pattern of change in resistance of leaves to low voltage, low frequency current during freezing was different in the frost-resistant and susceptible leaves. In tissue sections from both types of leaves, cells freeze extracellularly at cooling velocities lower than 5 C per minute. Cells from leaves of resistant plants showed a higher osmotic pressure but not a higher water permeability than those from susceptible plants. The extent of injury caused by even very slow freezing was greater than that caused by equivalent isopiestic desiccation, particularly in susceptible leaves. The higher osmotic pressure in cells of leaves from resistant plants can account for the greater desiccation resistance but not for the frost resistance observed.     

Adaptation of photosystem II to high and low light in wild-type and triazine-resistant Canola plants: analysis by a fluorescence induction algorithm

Plants of wild-type and triazine-resistant Canola (Brassica napus L.) were exposed to very high light intensities and after 1?day placed on a laboratory table at low light to recover, to study the kinetics of variable fluorescence after light, and after dark-adaptation. This cycle was repeated several times. The fast OJIP fluorescence rise curve was measured immediately after light exposure and after recovery during 1?day in laboratory room light. A fluorescence induction algorithm has been used for resolution and analysis of these curves. This algorithm includes photochemical and photo-electrochemical quenching release components and a photo-electrical dependent IP-component. The analysis revealed a substantial suppression of the photo-electrochemical component (even complete in the resistant biotype), a partial suppression of the photochemical component and a decrease in the fluorescence parameter F (o) after high light. These effects were recovered after 1?day in the indoor light.     

Heat Shock Proteins in Two Lines of Zea mays L. That Differ in Drought and Heat Resistance

Synthesis of heat shock proteins (HSPs) in the leaves of a drought- and heat-resistant (line ZPBL 1304), and a drought- and heat-sensitive (line ZPL 389) line of maize (Zea mays L.) was studied under two environmental stress treatments: (a) soil drying and high temperature and (b) high temperature. In the first treatment 13-day-old plants were exposed to 7-day soil drying followed by high temperature stress (45°C), and in the second treatment 20-day-old plants were exposed to high temperature stress (45°C). Second leaves were labeled with [³⁵S]methionine. During the labeling period line ZPBL 1304 showed no signs of leaf dehydration under soil drying and high temperature stress conditions. In contrast, line ZPL 389 was dehydrated 23%, as determined by relative water content. Incorporation of [³⁵S]methionine into protein was greater in the resistant than in the sensitive line in both treatments. The pattern of synthesis of HSPs in the two lines was similar in treatments 1 and 2. Both lines synthesized a high molecular mass set and a low molecular mass set of HSPs. Proteins from both sets from both lines of maize appeared similar to each other, with respect to the molecular mass. Heated plants of the drought- and heat-resistant line ZPBL 1304 synthesized a band of HSP(s) of approximately 45 kilodaltons which was not found in heated plants of the drought and heat sensitive line ZPL 389. This is the first report on qualitative intraspecific difference in the synthesis of HSPs in maize.     

Effects of growth temperture on photosynthetic carbon metabolism in green plants I. Photosynthetic activites of various plants acclimatized to varied temperatures

In wheat, pea, barley, broad bean and rape, the photosyntheticcapacities in the leaves of plants acclimatized to a highertemperature (20–25?C) were much higher than those in thesame plants grown at low outdoor temperatures in winter (meanairtemperature, 5–7?C). On transferring the cold-grown wheat plants (vats, 5–7?C)to the higher temperature (25/20?C), the Photosynthetic rateof laves remained unchanged for the first 8 hr, then graduallyincreased to attain after 16 hr a maximum level which was thesame as that in wheat plants grown at the higher temperature(growth box, 20–25?C). When intact wheat without soilwas taken from the cold winter field and the attached leaveswere placed in the chamber at 25?C, the Photosyntheic rate ofthe attached leaves increased sluggishly for 2 hr, then remarkablyincreased to attain the maximum level 9 hr afer transferralto the chamber. When the leaves detached from wheat grown inthe winter field were transferred to the assimilation chamberkept at 25?C, the rate started to increase without a lag periodand attained the maximum level within 3 hr. The optimum temperaturefor photosynthesis shifted in parallel with the rise of airtemperature under which the wheat had been grown. The slopes of increase in the photosynthetic rates with increasingintensity of illumination wwere practically the same in wheatgrown under different temperatures. It was found that the total amount of sucrose in wheat grownat low temperatures in the winter was higher than that in thosegrown at the high temperature. ¹Present address: Department of Botany, Faculty of Science,University of Tokyo, Tokyo, Japan. (Received July 19, 1973; )     

Temperature dependence of photosynthesis in Arabidopsis plants with modifications in Rubisco activase and membrane fluidity

Net photosynthesis (Pn) is reversibly inhibited at moderately high temperature. To investigate this further, we examined the effects of heat stress on Arabidopsis plants in which Rubisco activase or thylakoid membrane fluidity has been modified. During heating leaves from 25 to 40 degrees C at 250 ppm CO2 and 1% O2, the wild-type (WT), plants expressing the 43 kDa isoform only (rwt43), and plants accumulating activase 40% of WT (R100) exhibited similar inhibitions in the Pn and Rubisco activation state. Despite better membrane integrity than WT, plants having less polyunsaturation of thylakoid lipids (fad7/8 double mutant) failed to maintain greater Pn than the WT. Plants expressing the 46 kDa isoform only (rwt46) exhibited the most inhibition, but plants expressing a 46 kDa isoform incapable of redox regulation (C411A) were similar to the WT. The null mutant (rca) exhibited a continuous decline in Pn. As measured by fluorescence, electron transport activity decreased concomitantly with Pn but PSII was not damaged. Following a quick recovery to 25 from 40 degrees C, whereas most lines recovered 90% Pn, the rwt46 and rca lines recovered only to 59 and <10%, respectively. As measured by NADP-malate dehydrogenase activation, after an initial increase at 30 degrees C, stromal oxidation in the WT and rwt46 plants did not increase further as Pn decreased. These results provide additional insight into the role of Rubisco activation and activase in the reversible heat inhibition of Pn.     

Abscisic-acid in triazine-resistant and susceptible poa annua

Abscisic-acid (ABA) content in leaves and seeds were determined in two reciprocal hydbrids of cross between a triazine-resistant and a susceptible Poa annua. ABA in leaves appeared to be regulated by at least one major nuclear allele whilst ABA content in seeds appeared to maternally segregate with the cytoplasm. The lower ABA content found in seeds of the resistant parent and the resistant hybrid could be a secondary effect of the mutation that confers the resistance to the triazines.     

Photosynthetic Decline from High Temperature Stress during Maturation of Wheat : II. Interaction with Source and Sink Processes

High temperature stress reduces grain growth in wheat (Triticum aestivum L.) by altering source activity and sink capacity. The impact of stress on source and sink interactions in two wheat cultivars of differing source thermotolerance was monitored by analysis of chlorophyll fluorescence transients, Fv (variable fluorescence) and PSM (peak, stationary, maximum), of attached flag leaves on intact and decapitated tillers grown at optimum (20°C) and stress (35°C) temperatures after anthesis. The thermotolerant cultivar Waverly had reduced Fv and PS quenching and a large increase of SM during heat stress. The less thermotolerant cultivar, Len, exhibited increased Fv and PS quenching and a small increase of SM. Fluorescence induction was similar in intact and decapitated tillers of Len, indicating diminished sinksource interaction during heat stress. The present results and previous observations of photosynthetic activities indicate that cyclic electron transport and photophosphorylation in flag leaves of the thermotolerant cultivar were stimulated by sink demand (increased SM in intact plants). Reduced grain development in the thermolabile cultivar resulted from limited capacity to support cyclic electron transport and photophosphorylation (slight increase in SM of intact plants and large reduction of Cytochrome f/b₆-mediated electron transport capacity). It was concluded that heat stress injures the photosynthetic apparatus during reproductive growth of wheat and that diminished source activity and sink capacity may be equally important in reducing productivity.     

Effects of Growth Temperature on the Thermal Stability of the Photosynthetic Apparatus of Atriplex lentiformis (Torr.) Wats

High growth temperatures induced a substantial increase in the thermal stability of the photosynthetic apparatus of Atriplex lentiformis. This was manifested as a much reduced inhibition of light-saturated photosynthesis and the initial slope of the light-dependence curves by exposure to high temperatures in high as compared to moderate temperature-grown plants. Heat treatment at 46 C of leaves from moderate temperature-grown plants resulted in a marked reduction in photosystem II activities of chloroplasts isolated from them. In contrast, heat treatment of leaves from high temperature-grown plants resulted in no reduction of photosystem II activities. In vivo estimates of photosystem II functioning, the 515 nm light-induced absorbance change, and the ratio initial to maximum fluorescence (F₀/F_max) indicated a similar increase in the thermal stability of photosystem II in high temperature-grown plants.     

Functional plasticity of photosynthetic apparatus and its resistance to photoinhibition in <Emphasis Type="Italic">Plantago media</Emphasis>

Morphological and functional characteristics of Plantago media L. leaves were compared for plants growing at different light regimes on limestone outcrops in Southern Timan (62°45′N, 55°49′E). The plants grown in open areas under exposure to full sunlight had small leaves with low pigment content and high specific leaf weight; these leaves exhibited high photosynthetic capacity and elevated water use efficiency at high irradiance. The maximum photochemical activity of photosystem II (F _v/F _m) in leaves of sun plants remained at the level of about 0.8 throughout the day. The photosynthetic apparatus of sun plants was resistant to excess photosynthetically active radiation, mostly due to non-photochemical quenching of chlorophyll fluorescence (qN). This quenching was promoted by elevated deepoxiation of violaxanthin cycle pigments. Accumulation of zeaxanthin, a photoprotective pigment in sun plant leaves was observed already in the morning hours. The plant leaves grown in the shade of dense herbage were significantly larger than the sun leaves, with pigment content 1.5–2.0 times greater than in sun leaves; these leaves had low qN values and did not need extensive deepoxidation of violaxanthin cycle pigments. The data reveal the morphophysiological plasticity of plantain plants in relation to lighting regime. Environmental conditions can facilitate the formation of the ecotype with photosynthetic apparatus resistant to photoinhibition. Owing to this adjustment, hoary plantain plants are capable of surviving in ecotopes with high insolation.     

Heat Emission as a Protective Mechanism against High-irradiance Stress in Sugar Maple Leaves

High-irradiance (HI) induced changes in heat emission, fluorescence, and photosynthetic energy storage (EST) of shade grown sugar maple (Acer saccharum Marsh.) saplings were followed using modulated photoacoustic and fluorescence spectroscopic techniques. HI-treatment at 900-4400 µmol m-2 s-1 for 15 min caused an increase in heat emission and a decrease in EST. In some leaves, HI-treatment of 900 µmol m-2 s-1 for 1 min induced a rapid increase in heat emission with a marginal decrease in EST. Parallel to the increase in heat emission, there was a decrease in fluorescence, and this phenomenon was reversible in darkness. Quenching of thermal energy dissipation and a recovery in EST were observed during the first 15 min after the HI-treatment. This down-regulation of photochemical activity and its recovery may be one of the photoprotective mechanisms in shade grown sugar maple plants. The increase in thermal energy dissipation was greater in the red absorbing long wavelength (640-700 nm) region than in the blue absorbing short wavelength region of photosynthetically active excitation radiation. The photochemical activity was affected more in short wavelengths (400-520 nm) than in the long wavelength region of the spectrum. This can be due to the migration of light-harvesting chlorophyll (Chl) a/b protein complex from photosystem (PS) 2 to PS1 and/or to the disconnection of carotenoid pool from Chls in the pigment bed of photosynthetic apparatus.     

Investigations on heat resistance of spinach leaves

Exposure of spinach plants to high temperature (35° C) increased the heat resistance of the leaves by about 3° C. This hardening process occurred within 4 to 6 h, whereas dehardening at 20°/15° C required 1 to 2 days. At 5° C dehardening did not take place. Hardening and dehardening occurred in both the dark and the light. The hardiness was tested by exposure of the leaves to heat stress and subsequent measurements of chlorophyll fluorescence induction and light-induced absorbance changes at 535 nm on the leaves and of the photosynthetic electron transport in thylakoids isolated after heat treatment. Heat-induced damage to both heat-hardened and non-hardened leaves seemed to consist primarily in a breakdown of the membrane potential of the thylakoids accompanied by partial inactivation of electron transport through photosystem II. The increase in heat resistance was not due to temperature-induced changes in lipid content and fatty acid composition of the thylakoids, and no conspicuous changes in the polypeptide composition of the membranes were observed. Prolonged heat treatment at 35° C up to 3 days significantly decreased the total lipid content and the degree of unsaturation of the fatty acids of membrane lipids without further increase in the thermostability of the leaves. Intact chloroplasts isolated from heat-hardened leaves retained increased heat resistance. When the stroma of the chloroplasts was removed, the thermostability of the thylakoids was decreased and was comparable to the heat resistance of chloroplast membranes obtained from non-hardened control plants. Compartmentation studies demonstrated that the content of soluble sugars within the chloroplasts and the whole leaf tissue decreased as heat hardiness increased. This indicated that in spinach leaves, sugars play no protective role in heat hardiness. The results suggest that changes in the ultrastructure of thylakoids in connection with a stabilizing effect of soluble non-sugar stroma compounds are responsible for acclimatization of the photosynthetic apparatus to high temperature conditions. Changes in the chemical composition of the chloroplast membranes did not appear to play a role in the acclimatization.Abbreviations DGDG digalactosyl diglyceride - MGDG monogalactosyl diglyceride - PG phosphatidyl glycerol - PGA 3-phosphoglyceric acid Dedicated to Professor Wilhelm Simonis, Würzburg, on the occasion of his 70th birthday     

亚热带地区竞争型和忍耐型树种叶片可溶性有机质数量及光谱学特征

气候变化下,不同生态策略的树种对环境变化有着不同的响应能力,影响其叶片淋溶产生的DOM(Dissolved organic matter)的数量和质量,进而影响土壤的养分循环。通过探究亚热带地区不同生态策略树种叶片DOM数量及光谱学特征的差异,评估不同数量和结构特征DOM输入到土壤对养分循环的影响。本研究选取6种树种鲜叶进行浸提,其中竞争型(Competitive,C)和忍耐型(Stress-tolerant,S)各3种(树参(Dendropanax dentiger),黄绒润楠(Machilus grijsii),黄牛奶树(Symplocos cochinchinensis(Lour.)),细柄阿丁枫(Altingia gracilipes),丝栗栲(Castanopsis fargesii)和罗浮栲(Castanopsis faberi))。通过溶解性有机碳(Dissolved organic carbon,DOC)、溶解性有机氮(Dissolved organic nitrogen,DON)表征DOM的数量特征,通过紫外吸收值(Special Ultraviolet-Visible Absorption,SUVA),腐殖化指标(Humification index,HIX)和傅里叶红外光谱(Fouriertransform infrared,FTIR)等光谱指标表征DOM质量特征。结果表明:不同生态策略树种的叶浸提液中可溶性有机碳浓度无显著差异,但是C策略树种浸提液中可溶性有机氮浓度大于S策略的DON浓度。此外,S策略的芳香化指数(Aromatic index,AI)和腐殖化指数(HIX)均高于C策略。C策略树种的发射荧光强度也高于S策略,说明C策略树种DOM腐殖化程度较低,易分解物质含量高;S策略难分解物质多,腐殖化程度较高。傅里叶红外光谱结果表明,各树种叶浸提的DOM存在相似的吸收峰,其中以H键键合的—OH伸缩振动最强且C策略树种结果相对简单,验证了荧光光谱的结果。总体而言,与C策略相比,S策略树种叶片浸提的DOM结构更复杂,养分含量更高。这可能是因为,S策略树种对环境变化具有更高的适应性。由于其DOM结构相对复杂,输入土壤后减缓土壤碳周转速率,在未来气候变化情景下,S策略树种可能有利于土壤碳汇的形成。     

Response of light- and dark-grown callus of atrazine-resistant and susceptible rapeseed (Brassica napus) to varying concentrations of atrizine

Callus cultures initiated with tissue of triazine-resistant and susceptible lines of Brassica napus L. were cultured in the presence of atrazine (10^-5 to 10^-4 M) under a 16-h photoperiod or in continuous darkness. On atrazine-free media callus growth was characteristically greater for the light-grown cultures. On media containing atrazine, growth of callus from triazine-resistant and susceptible rapeseed cultured in the dark did not differ significantly. Addition of atrazine to the culture medium resulted in a significant reduction in the growth of light-grown callus of the susceptible genotype to a level equivalent to that of the dark-grown cultures. Atrazine had no effect on the growth of light-grown callus initiated with triazine-resistant rapeseed.