Chlorophyll a Fluorescence

... Michael E. Loik a , ¶ , Travis E. Huxman c , b , Erik P. Hamerlynck d , b and Stanley D. Smith b. ... 19. ME Loik, CD St. Onge and J. Rodgers, Post-fire recruitment of Yucca brevifolia and Yucca schidigera in Joshua Tree National Park, California. ...

The cold stress effect on early vigour and photosynthesis efficiency was evaluated for five industrial chicory varieties with contrasting early vigour. The relationships between the growth and physiological parameters were assessed. The varieties were examined at three growth temperatures: 16 (reference), 8 (intermediate) and 4 °C (stress). The effect was measured using physiological processes (growth, photosynthesis, chlorophyll a fluorescence), and pigment content. The analysis of the measured growth parameters (dry leaf and root mass, and leaf area) indicated that temperature had a significant effect on the varieties, but the overall reaction of the varieties was similar with lowering temperatures. The photosynthesis and chlorophyll a fluorescence measurements revealed significant changes for the photosynthesis (maximum net photosynthesis, quantum efficiency, light compensation point and dark respiration) and chlorophyll a fluorescence parameters (photochemical and non-photochemical quenching) with lowering temperatures for Hera and Eva, two extremes in youth growth. No significant differences could be found between the extremes for the different temperatures. The pigment content analysis revealed significant differences at 4 °C in contrast to 16 and 8 °C, especially for the xanthophyll/carotenoid pool, suggesting a protective role. Subsequently, the relationship between the physiological processes was evaluated using principal component analysis. At 4 °C, 2 principal components were detected with high discriminating power for the varieties and similar classification of the varieties as determined in the growth analysis. This provides a preview on the possible relationships between photosynthesis and growth for industrial chicory at low temperatures.

The photosynthetic characteristics of four transgenic rice lines over-expressing rice NADP-malic enzyme (ME), and maize phosphoenolpyruvate carboxylase (PC), pyruvate,orthophosphate dikinase (PK), and PC+PK (CK) were investigated using outdoor-grown plants. Relative to untransformed wild-type (WT) rice, PC transgenic rice exhibited high PC activity (25-fold increase) and enhanced activity of carbonic anhydrase (more than two-fold increase), while the activity of ribulose-bisphosphate carboxylase/oxygenase (Rubisco) and its kinetic property were not significantly altered. The PC transgenic plants also showed a higher light intensity for saturation of photosynthesis, higher photosynthetic CO(2) uptake rate and carboxylation efficiency, and slightly reduced CO(2) compensation point. In addition, chlorophyll a fluorescence analysis indicates that PC transgenic plants are more tolerant to photo-oxidative stress, due to a higher capacity to quench excess light energy via photochemical and...

Survival and recovery of the seagrass Halophila ovalis (R.Br.) Hook during and after light deprivation was investigated to assist in the interpretation of recent losses of Halophila spp. in Queensland, Australia. Light deprivation experiments were conducted in outdoor aquaria and in situ at two water depths. Halophila ovalis plants were deprived of light for a maximum of 30 days, and recovery processes were investigated for up to 18 days following 15 days of light deprivation. Measurements of H. ovalis biomass, storage carbohydrate concentrations, chlorophyll a+b concentrations, stable carbon isotopes ratios (δ13C) and chlorophyll a fluorescence parameters (F0, Fm and Fv/Fm) were made during and at the end of the light deprivation and recovery periods. Biomass declined after 3–6 days in the dark and complete plant death occurred after 30 days. During the recovery period, biomass continued to decline for a short duration of time before stabilising. Sugar concentrations declined rapidly for the first 2 days of light deprivation before stabilising, then increased rapidly during the recovery period. Chlorophyll a+b concentrations were sensitive to very small differences in light availability: concentration decreased in total darkness, remained unchanged at 0.1% of surface irradiance and increased at 0.5% of surface irradiance. Photochemical efficiency of photosystem II (Fv/Fm) remained unchanged during the light deprivation and recovery periods. The lack of response in δ13C during light deprivation indicated the cessation of carbon fixation. Decreased sugar utilisation after 2 days of light deprivation indicated a reduction in respiration and growth. Starch concentrations did not change during light deprivation, suggesting the inhibition of starch utilisation by anaerobic conditions within the plant. Plant death after 30 days was notably faster than previously reported for other species of seagrass. The rapid die-off may be due to a shortage of available carbohydrates or due to a build-up of the phytotoxic end products of anaerobic respiration. Overall, H. ovalis has a very limited tolerance to light deprivation when compared to larger species of seagrass. Consequently, the persistence of this species in coastal marine environments may be dependent upon the occurrence and duration of transient light deprivation events.

Florescence assessments of Sunflower (Helianthus annuus L.) genotypes in field under drought stress environment were studied. Climate change and low precipitation represents the main constraints in sunflower production in Pakistan. In present investigation two sunflower genotypes, viz S.28111 and SF0049 were selected to study their photosynthetic performance through non-destructive technique in field. Three treatments were applied to impose drought in plants i.e. irrigation after 6 days (D1), irrigation after 8 days (D2) and irrigation after 16 days (D3) with control irrigation after 4 days. Results revealed that drought stresses altered the electron transport rate through PSII (Fm/Fo), photochemical quenching (qP), efficiency of photosystem II (ΦPSII), linear electron transport rate (rETR), non-photochemical quenching (NPQ), size and number of active reaction centre of photosynthetic apparatus (Fv/Fo), driving forces (DFABS and DFCS) and performance indexes (PIABS and PICS) parameters that depends on the efficiency and yield of energy transfer and primary photochemistry. However, S.28111 maintained substantial quantum yield and enhanced photosynthetic performance under drought stress environment compared to SF0049. It is suggested that the assessment of photochemistry of PSII offers a practical and sensitive field screening regarding test for drought stress tolerance in sunflower. Results are discussed in relation to photosynthetic performance and florescence responses of sunflower genotypes in the drought stress environment.

To investigate the ability of pioneer and late-successional species to adapt to a strong light environment in a reforestation area, we examined the activities of antioxidant enzymes in relation to photosystem II, chlorophyll a fluorescence and photosynthetic pigment concentration for eight tropical tree species grown under 100% (sun) and 10% (shade) sunlight irradiation. The pioneer (early-succession) species (PS) were Cecropia

The response of barley (Hordeum vulgare L. cv. Akcent) to various photosynthetic photon flux densities (PPFDs) and elevated [CO2] [700 μmol (CO2) mol−1; EC] was studied by gas exchange, chlorophyll (Chl) a fluorescence, and pigment analysis. In comparison with barley grown under ambient [CO2] [350 μmol (CO2) mol−1; AC] the EC acclimation resulted in a decrease in photosynthetic capacity, reduced stomatal conductance, and decreased total Chl content. The extent of acclimation depression of photosynthesis, the most pronounced for the plants grown at 730 μmol m−2 s−1 (PPFD730), may be related to the degree of sink-limitation. The increased non-radiative dissipation of absorbed photon energy for all EC plants corresponded to the higher de-epoxidation state of xanthophylls only for PPFD730 barley. Further, a pronounced decrease in photosystem 2 (PS2) photochemical efficiency (given as FV/FM) for EC plants grown at 730 and 1 200 μmol m−2 s−1 in comparison with AC barley was related to the reduced epoxidation of antheraxanthin and zeaxanthin back to violaxanthin in darkness. Thus the EC conditions sensitise the photosynthetic apparatus of high-irradiance acclimated barley plants (particularly PPFD730) to the photoinactivation of PS2.

After briefly describing my early collaborative work at the University of Allahabad, that had laid the foundation of my research life, I present here some of our research on photosynthesis at the University of Illinois at Urbana-Champaign,randomly selected from light absorption to NADP+ reduction in plants, algae, and cyanobacteria. These include the fact that (i) both the light reactions I and II are powered by light absorbed by chlorophyll (Chl) a of different spectral forms; (ii)nlight emission (fluorescence, delayed fluorescence, andnthermoluminescence) by plants, algae, and cyanobacteria providesndetailed information on these reactions and beyond; (iii) primary photochemistry in both the photosystems I (PS I) and IIm(PS II) occurs within a few picoseconds; and (iv) most importantly, bicarbonate plays a unique role on the electron acceptor
side of PS II, specifically at the two-electron gate of PS II. Currently, the ongoing research around the world is, and should
be, directed towards making photosynthesis better able to deal with the global issues (such as increasing population, dwindling resources, and rising temperature) particularly through genetic modification. However, basic research is necessary to
continue to provide us with an understanding of the molecular mechanism of the process and to guide us in reaching our goals of increasing food production and other chemicals we need for our lives.

This chapter investigates the use of chlorophyll a fluorescence to better understand changes in the regulation of photosynthetic electron transport. It describes the different electron pathways utilised by photosynthetic organisms, including pathways used in photosynthesis as well as alternative electron cycling (AEC). The major photoprotective processes are described, in particular, non-photochemical quenching (NPQ) and its three components, energy-dependent quenching (qE), state-transition quenching (qT), and photoinhibition (qI). Fluorescence and NPQ responses to light stress are compared across a higher plant, diatom and cyanobacteria. Photosynthesis is a complex interaction of complementary processes making the identification and isolation of a particular photosynthetic pathway or process inherently difficult. Therefore, we describe the use of chemicals which allow for the differentiation of mechanistic photosynthetic processes, such as electron transport pathways, CO2 fixation and the use of trans-thylakoid proton gradients, which can be effectively understood and quantified using chlorophyll fluorescence detection techniques.

Assessments of photosynthetic activity in marine plants can now be made in situ using a newly developed, submersible, pulse-amplitude modulated (PAM) fluorometer: Diving-PAM. PAM fluorometry provides a measure of chlorophyll a fluorescence using rapid-light curves in which the electron-transport rate can be determined for plants exposed to ambient light conditions. This technique was used to compare the photosynthetic responses of seagrasses near Rottnest Island, Western Australia. Several fluorescence parameters were measured as a function of time of day and water depth; electron-transport rate (ETR), quantum yield, photochemical quenching and non-photochemical quenching and Photosystem II (PSII) photochemical efficiency (F v :F m ratio) were measured. Results indicate that recent light-history plays a crucial role in seagrass photosynthetic responses. Maximum ETR of Posidonia australis, Amphibolis antarctica and Halophila ovalis is influenced by the irradiance during the diurnal cycle, with low rates at dawn and dusk (<10 μmol electron m−2 s−1), highest rates in late morning (40 to 60 μmol electron m−2 s−1) and a mid-day depression. Maximum ETR and PSII photochemical efficiency varied widely between seagrass species and were not correlated. A comparison of photochemical to non-photochemical quenching indicated that seagrasses in shallow water receiving high light have a high capacity for non-photochemical quenching (e.g. light protection) compared to seagrasses in deep water. These results indicate that in situ measurements of photosynthesis will provide new insights into the mechanisms and adaptive responses of marine plants.

Surface property distributions were mapped in the Mississippi River plume during May and August 1993 while following surface drifters. Prevailing winds were the primary factor controlling the orientation of the plume. In May, under typical southeasterly winds, the plume turned anticyclonically towards the coast, while in August, under anomalous westerly winds, the plume turned east. Remote imagery of sea surface temperature and suspended sediments confirmed the direction of the plume. Optimally interpolated maps of surface salinity, temperature, chlorophyll a fluorescence, and transmissivity from underway sampling, and periodic nutrient samples, reveal the plume structure. In May concentrations of nitrate, silicate, and phosphate decreased linearly with increasing salinity. Chlorophyll a increased to peak concentrations of 10 μg 1-1 in the plume, although higher pigment biomass was observed near the coast. In August nitrate and silicate concentrations decreased conservatively near the mouth of SW Pass, except where pigment biomass was enhanced in a convergent surface front. Surface nutrient concentrations in the plume also decreased with increasing salinity. The observations provide the first Lagrangian view of surface property distributions in the Mississippi River plume, and indicate that significant temporal variability exists in physical and biological properties within a day after waters are discharged from the river delta.

The interactions among water content, chlorophyll a fluorescence emission, xanthophyll interconversions and net photosynthesis were analyzed during dehydration in desiccation-tolerant Frullania dilatata (L.) Dum. and desiccation-intolerant Pellia endiviifolia (Dicks) Dum. Water loss led to a progressive suppression of photosynthetic carbon assimilation in both species. Their chlorophyll fluorescence characteristics at low water content were: low photosynthetic quantum conversion efficiency, high excitation pressure on photosystem II and strong non-photochemical quenching. However, dissipation activity was lower in P. endiviifolia and was not accompanied by a rise in the concentration of de-epoxidised xanthophylls as F. dilatata. The photosynthetic apparatus of F. dilatata remained fully and speedily recuperable after desiccation in as indicated by the restoration of chlorophyll fluorescence parameters to pre-desiccation values upon rehydration. A lack of recovery upon remoistening of P. endiviifolia indicated permanent and irreversible damage to photosystem II. The results suggest that F. dilatata possesses a desiccation-induced zeaxanthin-mediated photoprotective mechanism which might aid photosynthesis recovery when favourable conditions are restored by alleviating photoinhibitory damage during desiccation. This avoidance mechanism might have evolved as an adaptative response to repeated cycles of desiccation and rehydration that represent a real threat to photosynthetic viability.