photochemical yield
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2020 ◽  
Vol 273 ◽  
pp. 109574
Author(s):  
Juliana Bezerra Martins ◽  
José Amilton Santos Júnior ◽  
Lucas Yago de Carvalho Leal ◽  
Martha Katharinne Silva Souza Paulino ◽  
Edivan Rodrigues de Souza ◽  
...  

Polar Biology ◽  
2020 ◽  
Vol 43 (10) ◽  
pp. 1453-1467
Author(s):  
Friederike Gehrmann ◽  
Iida-Maria Lehtimäki ◽  
Heikki Hänninen ◽  
Timo Saarinen

Abstract In tundra ecosystems, snow cover protects plants from low temperatures in winter and buffers temperature fluctuations in spring. Climate change may lead to reduced snowfall and earlier snowmelt, potentially exposing plants to more frequent and more severe frosts in the future. Frost can cause cell damage and, in combination with high solar irradiance, reduce the photochemical yield of photosystem II (ΦPSII). Little is known about the natural variation in frost exposure within individual habitats of tundra plant populations and the populations’ resilience to this climatic variation. Here, we assessed how natural differences in snowmelt timing affect microclimatic variability of frost exposure in habitats of the evergreen Vaccinium vitis-idaea in sub-Arctic alpine Finland and whether this variability affects the extent of cell damage and reduction in ΦPSII. Plants in early melting plots were exposed to more frequent and more severe frost events, and exhibited a more pronounced decrease in ΦPSII, during winter and spring compared to plants in late-melting plots. Snowmelt timing did not have a clear effect on the degree of cell damage as assessed by relative electrolyte leakage. Our results show that sub-Arctic alpine V. vitis-idaea is currently exposed to strong climatic variation on a small spatial scale, similar to that projected to be caused by climate change, without significant resultant damage. We conclude that V. vitis-idaea is effective in mitigating the effects of large variations in frost exposure caused by differences in snowmelt timing. This suggests that V. vitis-idaea will be resilient to the ongoing climate change.


Plants ◽  
2020 ◽  
Vol 9 (7) ◽  
pp. 825 ◽  
Author(s):  
Parvaiz Ahmad ◽  
Mohammed Nasser Alyemeni ◽  
Asma A. Al-Huqail ◽  
Moneerah A. Alqahtani ◽  
Leonard Wijaya ◽  
...  

Accumulation of arsenic (As) in soils is increasing consistently day-by-day, which has resulted in increased toxicity of this element in various crop plants. Arsenic interferes with several plant metabolic processes at molecular, biochemical and physiological levels, which result in reduced plant productivity. Hence, the introduction of novel ameliorating agents to combat this situation is the need of the hour. The present study was designed to examine the effect of zinc oxide nanoparticles (ZnO–NPs) in As-stressed soybean plants. Various plant growth factors and enzymes were studied at varying concentrations of As and ZnO–NPs. Our results showed that with the application of ZnO–NPs, As concentration declined in both root and shoot of soybean plants. The lengths of shoot and root, net photosynthetic rate, transpiration, stomatal conductance, photochemical yield and other factors declined with an increase in external As level. However, the application of ZnO–NPs to the As-stressed soybean plants resulted in a considerable increase in these factors. Moreover, the enzymes involved in the ascorbate–glutathione cycle including superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and glutathione reductase (GR) showed a significant increase in their activity with the application of ZnO–NPs to the As-stressed plants. Hence, our study confirms the significance of ZnO–NPs in alleviating the toxicity of As in soybean plants.


2020 ◽  
Author(s):  
Léna Beauzamy ◽  
Jérôme Delacotte ◽  
Benjamin Bailleul ◽  
Kenya Tanaka ◽  
Shuji Nakanishi ◽  
...  

ABSTRACTMicrobial solar cells that mainly rely on the use of photosynthesic organisms are a promising alternative to photovoltaics for solar electricity production. In that way, we propose a new approach involving electrochemistry and fluorescence techniques. The coupled set-up Electro-Pulse-Amplitude-Modulation (“e-PAM”) enables the simultaneous recording of the produced photocurrent and fluorescence signals from the photosynthetic chain. This methodology was validated with a suspension of green alga Chlamydomonas reinhardtii in interaction with an exogenous redox mediatior (2,6-dichlorobenzoquinone; DCBQ). The balance between photosynthetic chain events (PSII photochemical yield, quenching) and the extracted electricity can be monitored overtime. More particularly, the non photochemical quenching induced by DCBQ mirrors the photocurrent. This set-up thus helps to distinguish the electron harvesting from some side effects due to quinones in real time. It therefore paves the way for future analyses devoted to the choice of the experimental conditions (redox mediator, photosynthetic organisms…) to find the best electron extraction.


Forests ◽  
2019 ◽  
Vol 10 (12) ◽  
pp. 1126 ◽  
Author(s):  
Jaana Luoranen ◽  
Laura Pikkarainen ◽  
Marja Poteri ◽  
Heli Peltola ◽  
Johanna Riikonen

For spring plantings, conifer seedlings are usually packed in closed cardboard boxes and freezer stored over winter. Additionally, seedlings are increasingly being stored in cardboard boxes in spring, summer, and autumn plantings in Finland. The aim of this study was to determine the maximum safe duration for the field storage of Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) container seedlings in closed cardboard boxes for different planting times (dates) in Nordic boreal conditions. In the first experiment, Norway spruce seedlings (85-cm3 peat plugs) were packed in cardboard boxes in August, September, or October, and, in the second experiment, in the middle of May. In the third Scots pine experiment, mini seedlings (30-cm3 peat plugs) were packed in May. In each experiment, the seedlings were stored in closed cardboard boxes in a nursery for one, three, seven, 14, and 21 days. The control seedlings were stored in open storage in the nursery. After storage, the seedlings were planted in a field. In all of the experiments, increased closed-box storage reduced the maximum photochemical yield of photosystem II (Fv/Fm) in the needles, and reduced root growth after planting. The frost hardiness was weakened in the Norway spruce seedlings that were stored in closed boxes for 21 days in August and October. In the spring experiments, prolonged storage increased the mortality of seedlings. Mortality rates were high in the autumn experiment due to the exceptionally warm and dry weather. Our conclusions, being based on the short term effects of field storage, are that conifer seedlings can be stored in closed boxes for only three days in August and about a week in September, October, and spring.


2018 ◽  
Vol 28 (4) ◽  
pp. 476-480 ◽  
Author(s):  
Chenping Xu ◽  
Beiquan Mou

Chitosan has become of interest as a crop biostimulant suitable for use in sustainable agriculture since it is biocompatible, biodegradable, environmentally friendly, and readily available in large quantity. Short-term (35 d after transplanting) effects of chitosan, applied as a soil amendment at 0%, 0.05%, 0.10%, 0.15%, 0.20%, or 0.30% (w/w), on lettuce (Lactuca sativa) growth, chlorophyll fluorescence, and gas exchange were evaluated in a growth chamber study. Chitosan at 0.05%, 0.10%, and 0.15% increased leaf area from 674 to 856, 847, and 856 cm2, and leaf fresh weight from 28.6 to 39.4, 39.1, and 39.8 g, respectively. Only chitosan at 0.05% and 0.10% increased leaf dry weight from 3.42 to 4.37 and 4.35 g, respectively, while chitosan at 0.30% decreased leaf number, area, fresh and dry weight. Chitosan at 0.10%, 0.15%, 0.20%, and 0.30% increased leaf chlorophyll index from 29.8 to 34.4, 35.4, 37.5, and 41.4, respectively. Chitosan at 0.20% and 0.30% increased leaf maximum photochemical efficiency and photochemical yield, and chitosan at 0.10%, 0.15% 0.20%, and 0.30% increased leaf electron transport rate. Leaf photosynthesis rate and stomatal conductance (gS) increased from 9.3 to 12.7, 14.0, and 16.6 μmol·m−2·s−1 carbon dioxide, and from 0.134 to 0.183, 0.196, and 0.231 mol·m−2·s−1, under chitosan at 0.15%, 0.20%, and 0.30%, respectively. The results indicated that chitosan, at appropriate application rates, enhanced lettuce growth, and might have potential to be used for sustainable production of lettuce.


2017 ◽  
Vol 5 (23) ◽  
pp. 4499-4506 ◽  
Author(s):  
Si-Eun Kim ◽  
Alex M. Jordan ◽  
LaShanda T. J. Korley ◽  
Jonathan K. Pokorski

This work describes the complex interplay between mechanical manipulation of coextruded fibers and the resulting photochemical yield of surface modification.


2016 ◽  
Vol 113 (5) ◽  
pp. 1156-1161 ◽  
Author(s):  
Kapil Amarnath ◽  
Doran I. G. Bennett ◽  
Anna R. Schneider ◽  
Graham R. Fleming

The first step of photosynthesis in plants is the absorption of sunlight by pigments in the antenna complexes of photosystem II (PSII), followed by transfer of the nascent excitation energy to the reaction centers, where long-term storage as chemical energy is initiated. Quantum mechanical mechanisms must be invoked to explain the transport of excitation within individual antenna. However, it is unclear how these mechanisms influence transfer across assemblies of antenna and thus the photochemical yield at reaction centers in the functional thylakoid membrane. Here, we model light harvesting at the several-hundred-nanometer scale of the PSII membrane, while preserving the dominant quantum effects previously observed in individual complexes. We show that excitation moves diffusively through the antenna with a diffusion length of 50 nm until it reaches a reaction center, where charge separation serves as an energetic trap. The diffusion length is a single parameter that incorporates the enhancing effect of excited state delocalization on individual rates of energy transfer as well as the complex kinetics that arise due to energy transfer and loss by decay to the ground state. The diffusion length determines PSII’s high quantum efficiency in ideal conditions, as well as how it is altered by the membrane morphology and the closure of reaction centers. We anticipate that the model will be useful in resolving the nonphotochemical quenching mechanisms that PSII employs in conditions of high light stress.


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