45 resultados para Compensatory photosynthetic response


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Different protocols of food deprivation were used to bring two groups of juvenile three-spined sticklebacks Gaslerosteus aculeatus to the same reduced body mass in comparison with a control group fed daily ad libitum. One group experienced I week or deprivation then 2 weeks on maintenance rations. The second group experienced I week of ad lithium feeding followed by 2 weeks of deprivation. The deprived groups were reduced to a mean mass ore. 80% of controls. The compensatory growth response shown when ad libitum feeding was resumed was independent of the trajectory by which the three-spined sticklebacks had reached the reduced body mass. The compensatory response was Sufficient to return the deprived groups to the mass and length trajectories shown by the control group within 4 weeks. There was full compensation for dry mass and total lipid, but incomplete compensation for lipid-free dry mass. Hyperphagia and increased growth efficiency were present in the re-feeding phase, but there was a lag of a week before the hyperphagia was established. The consistency of the compensatory response of immature three-spined sticklebacks provides a potential model system for the analysis and prediction of appetite and growth in teleosts. (C) 2003 The Fisheries Society of the British isles.

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Compensatory growth is a phase of accelerated growth apparent when favourable conditions are restored after a period of growth depression. To investigate if F-2 common 'all-fish' growth hormone gene transgenic common carp (Cyprinus carpio) could mount compensatory growth, a 9 week study at 29 degrees C was performed. The control group was fed to satiation twice a day throughout the experiment. The other two groups were deprived of feed for 1 or 2 weeks, respectively, and then fed to satiation during the re-feeding period. At the end of the experiment, the live masses of fish in the deprived groups were still significantly lower than those of the controls. During the re-feeding period, size-adjusted mean specific growth rates and mean feed intakes were significantly higher in the deprived fish than in the controls, indicating a partial compensatory growth response in these fish. No significant differences were found in food conversion efficiency between the deprived and control fish during re-feeding, suggesting that hyperphagia was the mechanism responsible for increased growth rates. The proximate composition of the deprived fish at the end of the experiment was similar to that of the control fish. This study is, to our knowledge, the first to report that fast-growing transgenic fish can achieve partial compensation of growth following starvation. (c) 2007 The Authors Journal compilation (c) 2007 The Fisheries Society of the British Isles.

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The compensatory responses of juvenile gibel carp and Chinese longsnout catfish to four cycles of 1 part of a study designed to determine feeding regimes that would maximise growth rates. Both species showed compensatory growth in the re-feeding periods. The compensation was not sufficient for the deprived fish to match the growth trajectories of controls fed to satiation daily. The compensatory growth response was more clearly defined in the later cycles. The deprived fish showed hyperphagia during the 2-week periods of re-feeding and the hyperphagic response was clearer in the later cycles. The hyperphagia tended to persist for both weeks of the re-feeding period. The gibel carp showed no difference in gross growth efficiency between deprived and control fish. In the catfish, the gross growth efficiency of the deprived fish was marginally higher than that of control fish, but the efficiency varied erratically from week to week. Over the experiment, the deprived fish achieved growth rates 75-80% of those shown by control fish, although fed at a frequency of 66%. There was no evidence of growth over-compensation with the deprivation-re-feeding protocol used in this study. (C) 2004 Elsevier B.V. All rights reserved.

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A mechanistic model is developed to present the photosynthetic response of phytoplankton to irradiance at the physiological level. The model is operated on photosynthetic units (PSU), and each PSU is assumed to have two states: reactive and activated. Light absorption that drives a reactive PSU into the activated state results from the effective absorption of the PSU. Transitions between the two states are asymmetrical in rate. A PSU in the reactive state becomes activated much faster than it recovers from the activated state to the reactive one. The turnover time for an activated PSU to transit into the reactive one is defined by the turnover time of the electron transport chain. The present model yields a photosynthesis-irradiance curve (PE-curve) in a hyperbola, which is described by three physiological parameters: effective cross-section (sigma (PSII)), turnover time of electron transport chain (tau) and number of PSUs (N). The PE-curve has an initial slope of sigma (PSII) x N, a half-saturated irradiance of 1/(sigma (PSII)), and a maximal photosynthetic rate of Nlc at the saturated irradiance. The PE-curve from the present model is comparable to the empirical function based on the target theory described by the Poisson distribution. (C) 2001 Academic Press.

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本文研究了富贵草对模拟光斑的光合响应、银杉对光的适应性以及大叶黄杨叶片内部光能利用梯度三个方面的问题。 1)研制了用于林内光环境调查和研究的光量子计组件。 关键词:光量子计,A/D板 2)以亚热带常绿阔叶林下一种常见的灌木富贵草为研究对象,利用气体交换和叶绿素荧光技术研究了其对模拟光斑的光合响应。在同样辐射通量(非光抑制)的情况下,光合诱导过程中光斑可以提高富贵草对光斑的利用能力(光斑诱导的碳同化量可高出对照48%)。叶绿素荧光测量结果表明:1)光斑与光斑之间的暗期发生了qN弛豫过程;2)暗期之后的光期光化学能量转换效率提高。强光光斑簇可以诱导富贵草光抑制的产生,但程度较连续光低。 关键词:模拟光斑, 叶绿素荧光, 光诱导过程 3)用高效液相色谱(HPLC)和77K低温荧光发射光谱技术来研究快速诱导组分发生的时间内光斑所导致NPQ (qN)降低的生理原因。在非光抑制条件下,光斑造成的NPQ (qN)降低的生理原因包括叶黄素循环的变化及LHCIIs聚集态的变化;此外低温荧光数据还显示光斑导致的PSII/PSI荧光产量比率要高于连续光,说明光斑导致植物对于光的利用增加。以上结果说明模拟光斑诱导了富贵草内囊体膜较低水平的能态。 关键词:模拟光斑,叶黄素,聚集态 4)用气体交换等技术测定了部分银杉幼树的生理生态指标,用鱼眼镜头测定了所测叶片的林冠开度(OP)。研究了沿林冠开度梯度的银杉幼树对光的适应性。银杉幼树在林窗边缘表现出较好的适应性,包括高的ISG(综合地上部分茎生长),高的HG(当年生树高生长速率),较高的LMA(单位叶片面积干物质重),较高的Pns(单位叶片干物质水平的净光合速率),高的单位叶片的碳同化速率,较高的截获光的单位叶片的叶面积等等,可以初步确定银杉属于Gap树种:在所测定的范围内(0. 00139%-0. 0109%)TN(土壤总氮量)明显不如OP对银杉幼树生长的影响大;综合的生态可塑性指标必须考虑具体的实验地情况、选取合适的形态学和生理学的因子、并结合多个相似生长环境下的树种来进行考虑。 关键词:林冠开度,生理生态指标,生态可塑性 5)分析了湖南八面山的银杉的某些光合特性,并比较了极郁闭( OP<4%)情况下银杉当年生叶片与大树顶端枝条(OP>30%)当年生叶片之间光合特性上的差异。极郁闭情况下银杉叶片生长出现黄化现象,但银杉幼苗又不耐强光。银杉幼苗一天的光合动态变化表明,银杉最大光合速率在早晨8:00左右,当光照超过光饱和点时,净光合速率迅速下降,其后略有回升,呈不太典型的双峰模式。气孔关闭与净光合速率的下降有密切的关系。早晨8:00到11:00间叶黄素循环运转,对光合系统起到一定保护作用。 关键词: 银杉,色素分析,光合作用 6)采用一种新方法来测量大叶黄杨叶片内部的绝对光能利用效率梯度的曲线。该方法基于光声光谱的深度分析(Depth-Analysis)理论,并结合了光纤微探测器的叶片光梯度测量结果。日本小檗(Berberis thunbergii DC.)叶片的光声光谱扫描显示了深度分析的精确性。实验结果表明:叶片内部利用光能效率最低处在栅栏组织和海棉组织之间(入射光能的0.026%-660nm红光);越靠近叶片的上表皮和下表皮,趋势显示叶片组织利用光能效率有上升的趋势(分别为0.092%,0.036%)。因此,不同叶肉组织绝对光能利用效率是不同的,该实验结果直接证实了Han &Vogelmann 1999b所提出的假设。 关键词: PA深度分析 叶片内部的光梯度 光化学损失 光吸收梯度

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基于长期观测资料,众多大气环流模型预测在二十一世纪末大气中二氧化碳浓度将达到700μmolmol'I,地球表面年平均温度也将升高1.5-4.OoC。水稻是亚洲的主要粮食作物,为世界近三分之一的人口提供食物能源。这项工作的目的,是利用人工模拟环境,预测在未来全球气候变化,二氧化碳及温度升高的条件下,水稻的光合生理反应及随之而来的对其产量的影响。本研究是美国环境署( EPA)与国际水稻研究所(IRRI)合作研究项目“Effects of UV-B and Global Climate Change on Rice”的一部分. 在这项研究中,采用了特殊设计并直接建立在水稻田间的开顶式气室(open-top chambers)。在此之前还没有这样大规模的在水稻主产区的此类模拟研究,水稻在气室中渡过了从萌发到收获的整个生长过程。模拟环境条件有三个浓度的二氧化碳(包括现有大气浓度,在此基础上升高200及300 μmolmol-l)和两个温度(即:现有大气温度及升高4度)共六个处理。供试水稻品种四个:IR72,IR65598-112-2,IR65600-42-5-2-BSI-313和N22。在实验中我们发现,水稻品种(如:1R72)单叶光合速率(以二氧化碳气体交换速率计)受二氧化碳浓度促进,在水稻营养生长期,二氧化碳及温度对其光合有协同促进作用.然而,随着花期的到来,在高温条件下,叶片光合能力(photosynthetic capacity)下降,出现光合适应现象(Photosynthetic acclirnation).水稻群体光合作用同样受到二氧化碳浓度促进,但在后期(Grain fill stage)这种促进作用消失;在高浓度二氧化碳下生长的大多数水稻品种的叶片中有较多的碳水化和物(可溶性糖和淀粉)积累.耐高温品种N22叶片中淀粉积累较少:叶片中氮素含量降低,同时发现Rubisco总活性相应降低,这与NCi曲线所示光合效率降低相吻合;通过叶片叶绿素荧光动力学测定,没有发现光系统光能转化效率的变化;水稻籽粒产量随二氧化碳浓度升高而增加,但温度升高使产量降低12.8-36.8%;不同品种对二氧化碳浓度的反应没有显著差别;在高温条件下,耐高温品生长在高二氧化碳浓度下表现良好。 本文系统地研究了水稻光合作用在二氧化碳及温度条件影响下,对二氧化碳浓度及光强变化的反应曲线,初次对水稻单叶与群体光合对二氧化碳浓度变化的反应做了实验性对比;讨论了温度升高对水稻在高浓度二氧化碳下发生光合适应的影响,对光合适应现象的可能机制做了探讨,并提出对未来大气二氧化碳浓度及温度升高条件下水稻适应品种筛选的可能方向。

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1. The importance of vertical mixing in modulating the impact of UVR on phytoplankton photosynthesis was assessed in a tropical, shallow lake in southern China from late winter to mid-spring of 2005. 2. Daily cycles of fluorescence measurements (i.e. photosynthetic quantum yield, Y) were performed on both 'static' and in situ samples. Static samples were of surface water incubated at the surface of the lake under three radiation treatments - PAB (PAR + UVR, 280-700 nm), PA (PAR + UV-A, 320-700 nm) and P (PAR, 400-700 nm). In situ samples were collected every hour at three different depths - 0, 0.5 and 1 m. 3. The general daily pattern was of a significant decrease in Y from early morning towards noon, with partial recovery in the afternoon. Samples incubated under static conditions always had lower Y than those under in situ conditions at the same time of the day. 4. Under stratified conditions, no overall impact of UVR impact could be detected in situ when compared with the static samples. Further rapid vertical mixing not only counteracted the impact of UVR but also stimulated photosynthetic efficiency. 5. Based on these measurements of fluorescence, the mixing speed of cells moving within the epilimnion was estimated to range between 0.53 and 6.5 cm min(-1). 6. These data show that mixing is very important in modulating the photosynthetic response of phytoplankton exposed to natural radiation and, hence, strongly conditions the overall impact of UVR on aquatic ecosystems.

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Individual juvenile three-spined sticklebacks Gasterosteus aculeatus and European minnow Phoxinus phoxinus, from sympatric populations, were subjected to four cycles of I week of food deprivation and 2 weeks of ad libitum feeding. Mean specific growth rate during the weeks of deprivation was negative and did not differ between species. The three-spined stickleback showed sufficient growth compensation to recover to the growth trajectory shown by control fish daily fed ad libitum. The compensation was generated by hyperphagia during the re-feeding periods, and in the last two periods of re-feeding, the gross growth efficiencies of deprived three-spined sticklebacks were greater than in control fish. The expression of the compensatory changes in growth and food consumption became clearer over the successive periods of re-feeding. The European minnow developed only a weak compensatory growth response and the mass trajectory of the deprived fish deviated more and more from the control trajectory During re-feeding periods, there were no significant differences in food consumption or gross growth efficiency between control and deprived European minnows. The differences between the two species are discussed in terms of the possible costs of compensatory growth, the control of growth and differences in feeding biology (C) 2003 The Fisheries Society of the British Isles.

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为揭示低温下光照对黄瓜光合作用的影响,在叶片水平对5℃ 100μmolm·-’·s-1和5℃黑暗处理4h后黄瓜叶片光合-光响应和光合-CO2响应进行了对比研究、结果表明,5℃黑暗处理4h使黄瓜叶片光饱和光合速率、表观光量子效率、CO2饱和光合速率以及梭化效率分别降低 22.5%、28.0%、31.3%和 37.2%,5℃ 100μmol·m-2·s-1使上述指标分别降低 56.1%、61.0%、54.0%和 54.3%,说明 100μmol·m-2·s-1光照明显加剧5℃低温对黄瓜叶片光合功能的伤害。进一步研究结果显示低温光照处理使黄瓜叶片 PSⅡ光合中心受到较严重的光抑制,类囊体跨膜质子梯度显著降低。对低温下光照对黄瓜叶片光合作用具有不良作用的原因进行了讨论。

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Photoinhibition is a central problem for the understanding of plasticity in photosynthesis vs. irradiance response. It effectively reduces the photosynthetic rate. In this contribution, we present a mechanistic model of algal photoinhibition induced by photodamage to photosystem-II. Photosystem-IIs (PSIIs) are assumed to exist in three states: open, closed and inhibited. Photosynthesis is closely associated with the transitions between the three states. The present model is defined by four parameters: effective cross section of PSII, number of PSIIs, turnover time of electron transfer chains and the ratio of rate constant of damage to that of repair of D1 proteins in PSIIs. It gives a photosynthetic response curve of phytoplankton to irradiance (PI-curve). Without photoinhibition, the PI-curve is in hyperbola with the first three parameters. The PI-curve with photoinhibition can be simplified to the same form as the hyperbola by replacing either the number of PSIIs with the number of functional PSIIs or the turnover time of electron transfer chains with the average turnover time.

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Previous studies on diurnal photosynthesis of macroalgal species have shown that at similar levels of photosynthetically active radiation (PAR, 400-700nm) the photosynthetic rate is lower in the afternoon than in the morning. However, the impacts of solar ultraviolet radiation (UVR, 280-400nm) have been little considered. We investigated the diurnal photosynthetic behaviour of the economically significant red alga Gracilaria lemaneiformis in the absence or presence of UV-A+B or UV-B with a flow-through system. While UV-A and UV-B, respectively, inhibited noontime Pmax by 22% and 14% on the sunny days, UV-A during sunrise (PAR below about 50Wm-2) increased the net photosynthesis by about 8% when compared with PAR alone. UV-A + PAR also resulted in higher apparent photosynthetic efficiency in the morning than in the afternoon period than PAR alone. Nevertheless, integrated daytime photosynthetic production under solar PAR alone was higher than with either PAR + UV-A+B or PAR + UV-A. Relative growth rate in the long term (9 days) matched the integrated photosynthetic production in that UV-A led to 9-15% and UV-B to 19-22% reduction, respectively. UV-absorbing compounds were found to be higher in the thalli exposed to PAR+UV-A+B than under PAR alone, reflecting a protective response to UVR.

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UV radiation is one of many harmful factors found in space that are detrimental to organisms on earth in space exploration. In the present work, we examined the role of antioxidant system in Nostoc sphaeroides Kutz (Cyanobacterium) and the effects of exogenously applied antioxidant molecules on its photosynthetic rate under UV-B radiation. It was found that UV-B radiation promoted the activity of antioxidant system to protect photosystem 11 (PSII) and exogenously applied antioxidant: sodium nitroprusside (SNP) and N-acetylcysteine (NAC) had an obvious protection on PSII activity under UV-B radiation. The activity of superoxide dismutase (SOD, EC 1.15.1.1), catalase (CAT, EC 1.11.1.6), peroxidase (POD, EC 1.11.1.7) and content of NIDA (malondialdehyde) and ASC (ascorbate) were improved by 0.5 mM and 1 mM SNP, but 0.1 mM SNP decreased the activity of antioxidant system. Addition of exogenous NAC decreased the activity of SOD, POD, CAT and the content MDA and ASC. In contrast, exogenously applied NAC increased GSH content. The results suggest that exogenous SNP and NAC may protect algae by different mechanisms: SNP may play double roles as both sources of reactive free radicals as well as ROS scavengers in mediating the protective role of PSII on algae under UV-B radiation. On the other hand, NAC functions as an antioxidant or precursor of glutathione, which could protect PSII directly from UV-B radiation. (c) 2007 COSPAR, Published by Elsevier Ltd. All rights reserved.