scholarly journals Defoliation Significantly Suppressed Plant Growth Under Low Light Conditions in Two Leguminosae Species

2022 ◽  
Vol 12 ◽  
Author(s):  
Ning Wang ◽  
Tianyu Ji ◽  
Xiao Liu ◽  
Qiang Li ◽  
Kulihong Sairebieli ◽  
...  
Keyword(s):  
Plant Growth ◽  
Combined Treatment ◽  
Chlorophyll Concentration ◽  
Light Stress ◽  
Early Period ◽  
Light Treatment ◽  
High Light ◽  
Herbivorous Insects ◽  
Light Conditions ◽  
Low Light

Seedlings in regenerating layer are frequently attacked by herbivorous insects, while the combined effects of defoliation and shading are not fully understood. In the present study, two Leguminosae species (Robinia pseudoacacia and Amorpha fruticosa) were selected to study their responses to combined light and defoliation treatments. In a greenhouse experiment, light treatments (L+, 88% vs L−, 8% full sunlight) and defoliation treatments (CK, without defoliation vs DE, defoliation 50% of the upper crown) were applied at the same time. The seedlings’ physiological and growth traits were determined at 1, 10, 30, and 70 days after the combined treatment. Our results showed that the effects of defoliation on growth and carbon allocation under high light treatments in both species were mainly concentrated in the early stage (days 1–10). R. pseudoacacia can achieve growth recovery within 10 days after defoliation, while A. fruticosa needs 30 days. Seedlings increased SLA and total chlorophyll concentration to improve light capture efficiency under low light treatments in both species, at the expense of reduced leaf thickness and leaf lignin concentration. The negative effects of defoliation treatment on plant growth and non-structural carbohydrates (NSCs) concentration in low light treatment were significantly higher than that in high light treatment after recovery for 70 days in R. pseudoacacia, suggesting sufficient production of carbohydrate would be crucial for seedling growth after defoliation. Plant growth was more sensitive to defoliation and low light stress than photosynthesis, resulting in NSCs accumulating during the early period of treatment. These results illustrated that although seedlings could adjust their resource allocation strategy and carbon dynamics in response to combined defoliation and light treatments, individuals grown in low light conditions will be more suppressed by defoliation. Our results indicate that we should pay more attention to understory seedlings’ regeneration under the pressure of herbivorous insects.

scholarly journals Color-Specific Recovery to Extreme High-Light Stress in Plants

Life ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 812
Author(s):  
Débora Parrine ◽  
Todd M. Greco ◽  
Bilal Muhammad ◽  
Bo-Sen Wu ◽  
Xin Zhao ◽  
...  
Keyword(s):  
Blue Light ◽  
Light Stress ◽  
Red Light ◽  
Light Treatment ◽  
High Light ◽  
Mrna Levels ◽  
Light Conditions ◽  
High Light Stress ◽  
General Response ◽  
The Impact

Plants pigments, such as chlorophyll and carotenoids, absorb light within specific wavelength ranges, impacting their response to environmental light changes. Although the color-specific response of plants to natural levels of light is well described, extreme high-light stress is still being discussed as a general response, without considering the impact of wavelengths in particular response processes. In this study, we explored how the plant proteome coordinated the response and recovery to extreme light conditions (21,000 µmol m−2 s−1) under different wavelengths. Changes at the protein and mRNA levels were measured, together with the photosynthetic parameters of plants under extreme high-light conditions. The changes in abundance of four proteins involved in photoinhibition, and in the biosynthesis/assembly of PSII (PsbS, PsbH, PsbR, and Psb28) in both light treatments were measured. The blue-light treatment presented a three-fold higher non-photochemical quenching and did not change the level of the oxygen-evolving complex (OEC) or the photosystem II (PSII) complex components when compared to the control, but significantly increased psbS transcripts. The red-light treatment caused a higher abundance of PSII and OEC proteins but kept the level of psbS transcripts the same as the control. Interestingly, the blue light stimulated a more efficient energy dissipation mechanism when compared to the red light. In addition, extreme high-light stress mechanisms activated by blue light involve the role of OEC through increasing PsbS transcript levels. In the proteomics spatial analysis, we report disparate activation of multiple stress pathways under three differently damaged zones as the enriched function of light stress only found in the medium-damaged zone of the red LED treatment. The results indicate that the impact of extreme high-light stress on the proteomic level is wavelength-dependent.

Changes in the Stoichiometry of Photosystem II Components as an Adaptive Response to High-Light and Low-Light Conditions during Growth

1986 ◽  
Vol 41 (5-6) ◽  
pp. 597-603 ◽  
Author(s):  
Aloysius Wild ◽  
Matthias Höpfner ◽  
Wolfgang Rühle ◽  
Michael Richter
Keyword(s):  
Photosystem Ii ◽  
Functional Organization ◽  
Photosynthetic Apparatus ◽  
High Light ◽  
Molar Ratio ◽  
Light Conditions ◽  
Low Light ◽  
Pigment System ◽  
Transport Chain ◽  
The One

The effect of different growth light intensities (60 W·m-2, 6 W·m-2) on the performance of the photosynthetic apparatus of mustard plants (Sinapis alba L.) was studied. A distinct decrease in photosystem II content per chlorophyll under low-light conditions compared to high-light conditions was found. For P-680 as well as for Oᴀ and Oв protein the molar ratio between high-light and low-light plants was 1.4 whereas the respective concentrations per chlorophyll showed some variations for P-680 and Oᴀ on the one and Oв protein on the other hand.In addition to the study of photosystem II components, the concentrations of PQ, Cyt f, and P-700 were measured. The light regime during growth had no effect on the amount of P-700 per chlorophyll but there were large differences with respect to PQ and Cyt f. The molar ratio for Cyt f and PQ between high- and low-light leaves was 2.2 and 1.9, respectively.Two models are proposed, showing the functional organization of the pigment system and the electron transport chain in thylakoids of high-light and low-light leaves of mustard plants.

scholarly journals Effects of alkalinity and salinity at low and high light intensity on hydrogen isotope fractionation of long-chain alkenones produced by <i>Emiliania huxleyi</i>

2017 ◽  
Vol 14 (24) ◽  
pp. 5693-5704 ◽  
Author(s):  
Gabriella M. Weiss ◽  
Eva Y. Pfannerstill ◽  
Stefan Schouten ◽  
Jaap S. Sinninghe Damsté ◽  
Marcel T. J. van der Meer
Keyword(s):  
Light Intensity ◽  
Environmental Conditions ◽  
Hydrogen Isotope ◽  
Isotope Fractionation ◽  
Emiliania Huxleyi ◽  
High Light Intensity ◽  
High Light ◽  
Light Conditions ◽  
Low Light ◽  
Long Chain

Abstract. Over the last decade, hydrogen isotopes of long-chain alkenones have been shown to be a promising proxy for reconstructing paleo sea surface salinity due to a strong hydrogen isotope fractionation response to salinity across different environmental conditions. However, to date, the decoupling of the effects of alkalinity and salinity, parameters that co-vary in the surface ocean, on hydrogen isotope fractionation of alkenones has not been assessed. Furthermore, as the alkenone-producing haptophyte, Emiliania huxleyi, is known to grow in large blooms under high light intensities, the effect of salinity on hydrogen isotope fractionation under these high irradiances is important to constrain before using δDC37 to reconstruct paleosalinity. Batch cultures of the marine haptophyte E. huxleyi strain CCMP 1516 were grown to investigate the hydrogen isotope fractionation response to salinity at high light intensity and independently assess the effects of salinity and alkalinity under low-light conditions. Our results suggest that alkalinity does not significantly influence hydrogen isotope fractionation of alkenones, but salinity does have a strong effect. Additionally, no significant difference was observed between the fractionation responses to salinity recorded in alkenones grown under both high- and low-light conditions. Comparison with previous studies suggests that the fractionation response to salinity in culture is similar under different environmental conditions, strengthening the use of hydrogen isotope fractionation as a paleosalinity proxy.

scholarly journals Occurrence of neoxanthin and lutein epoxide cycle in parasitic Cuscuta species.

2008 ◽  
Vol 55 (1) ◽  
pp. 183-190 ◽  
Author(s):  
Jerzy Kruk ◽  
Renata Szymańska
Keyword(s):  
Substrate Specificity ◽  
Xanthophyll Cycle ◽  
Higher Plants ◽  
Light Stress ◽  
High Light ◽  
Light Conditions ◽  
Strong Light ◽  
Zeaxanthin Epoxidase ◽  
Typical Response ◽  
Cuscuta Species

In the present study, xanthophyll composition of eight parasitic Cuscuta species under different light conditions was investigated. Neoxanthin was not detected in four of the eight species examined, while in others it occurred at the level of several percent of total xanthophylls. In C. gronovii and C. lupuliformis it was additionally found that the neoxanthin content was considerably stimulated by strong light. In dark-adapted plants, lutein epoxide level amounted to 10-22% of total xanthophylls in only three species, the highest being for C. lupuliformis, while in others it was below 3%, indicating that the lutein epoxide cycle is limited to only certain Cuscuta species. The obtained data also indicate that the presence of the lutein epoxide cycle and of neoxanthin is independent and variable among the Cuscuta species. The xanthophyll cycle carotenoids violaxanthin, antheraxanthin and zeaxanthin were identified in all the examined species and occurred at the level found in other higher plants. The xanthophyll and lutein epoxide cycle pigments showed typical response to high light stress. The obtained results also suggest that the ability of higher plants to synthesize lutein epoxide probably does not depend on the substrate specificity of zeaxanthin epoxidase but on the availability of lutein for the enzyme.

Is the in vivo Photosystem I Function Resistant to Photoinhibition? An Answer from Photoacoustic and Far-Red Absorbance Measurements in Intact Leaves

1991 ◽  
Vol 46 (11-12) ◽  
pp. 1038-1044 ◽  
Author(s):  
Michel Havaux ◽  
Murielle Eyletters
Keyword(s):  
Light Stress ◽  
Red Light ◽  
Light Treatment ◽  
High Light ◽  
Saturation Curve ◽  
Strong Light ◽  
Ps Ii ◽  
Fluorescence Measurements ◽  
Ps I

Abstract Preillumination of intact pea leaves with a strong blue-green light of 400 W m-2 markedly inhibited both photoacoustically monitored O2-evolution activity and PS II photochemistry as estimated from chlorophyll fluorescence measurements. The aim of the present work was to examine, with the help of the photoacoustic technique, whether this high-light treatment deteriorated the in vivo PS I function too. High-frequency photoacoustic measurements indicated that photochemical conversion of far-red light energy in PS I was preserved (and even transiently stimulated) whereas photochemical energy storage monitored in light exciting both PS I and PS II was markedly diminished. Low-frequency photoacoustic measurements of the Emerson enhancement showed a spectacular change in the PS II/PS I activity balance in favor of PS I. It was also observed that the linear portion of the saturation curve of the far-red light effect in the Emerson enhancement was not changed by the light treatment. Those results lead to the conclusion that, in contrast to PS II, the in vivo PS I photofunctioning was resistant to strong light stress, thus confirming previous suggestions derived from in vitro studies. Estimation of the redox state of the PS I reaction center by leaf absorbance measurements at ca. 820 nm suggested that, under steady illumination, a considerably larger fraction of PS I centers were in the closed state in high-light pretreated leaves as compared to control leaves, presumably allowing passive adjustment of the macroscopic quantum yield of PS I photochemis­ try to the strongly reduced photochemical efficiency of photoinhibited PS II.

Does Astaxanthin Protect Haematococcus against Light Damage?

1998 ◽  
Vol 53 (1-2) ◽  
pp. 93-100 ◽  
Author(s):  
Lu Fan ◽  
Avigad Vonshak ◽  
Aliza Zarka ◽  
Sammy Boussiba
Keyword(s):  
Light Intensity ◽  
Light Stress ◽  
Phosphate Starvation ◽  
High Light Intensity ◽  
High Irradiance ◽  
High Light ◽  
Protective Agent ◽  
Light Damage ◽  
Low Light ◽  
Very High

Abstract The photoprotective function of the ketocarotenoid astaxanthin in Haematococcus was questioned. When exposed to high irradiance and/or nutritional stress, green Haematococcus cells turned red due to accumulation of an immense quantity of the red pigment astaxanthin. Our results demonstrate that: 1) The addition of diphenylamine, an inhibitor of astaxanthin biosynthesis, causes cell death under high light intensity; 2) Red cells are susceptible to high light stress to the same extent or even higher then green ones upon exposure to a very high light intensity (4000 μmol photon m-2 s-1); 3) Addition of 1O2 generators (methylene blue, rose bengal) under noninductive conditions (low light of 100 (μmol photon m-2 s-1) induced astaxanthin accumulation. This can be reversed by an exogenous 1O2 quencher (histidine); 4) Histidine can prevent the accumulation of astaxanthin induced by phosphate starvation. We suggest that: 1) Astaxanthin is the result of the photoprotection process rather than the protective agent; 2) 1O2 is involved indirectly in astaxanthin accumulation process.

scholarly journals The Response Regulator RpaB Binds to the Upstream Element of Photosystem I Genes To Work for Positive Regulation under Low-Light Conditions in Synechocystis sp. Strain PCC 6803

2008 ◽  
Vol 191 (5) ◽  
pp. 1581-1586 ◽  
Author(s):  
Yurie Seino ◽  
Tomoko Takahashi ◽  
Yukako Hihara
Keyword(s):  
Photosystem I ◽  
Promoter Activity ◽  
Response Regulator ◽  
Core Promoter ◽  
High Light ◽  
Light Conditions ◽  
Low Light ◽  
Positive Regulation ◽  
Upstream Element ◽  
Pcc 6803

ABSTRACT The coordinated high-light response of genes encoding subunits of photosystem I (PSI) is achieved by the AT-rich region located just upstream of the core promoter in Synechocystis sp. strain PCC 6803. The upstream element enhances the basal promoter activity under low-light conditions, whereas this positive regulation is lost immediately after the shift to high-light conditions. In this study, we focused on a high-light regulatory 1 (HLR1) sequence included in the upstream element of every PSI gene examined. A gel mobility shift assay revealed that a response regulator RpaB binds to the HLR1 sequence in PSI promoters. Base substitution in the HLR1 sequence or decrease in copy number of the rpaB gene resulted in decrease in the promoter activity of PSI genes under low-light conditions. These observations suggest that RpaB acts as a transcriptional activator for PSI genes. It is likely that RpaB binds to the HLR1 sequence under low-light conditions and works for positive regulation of PSI genes and for negative regulation of high-light-inducible genes depending on the location of the HLR1 sequence within target promoters.

Interactions entre mitochondries et chloroplastes dans la cellule. II. Action du DBMIB, de l'antimycine A et du FCCP sur la spore de Funaria hygrometrica

1977 ◽  
Vol 55 (12) ◽  
pp. 1650-1659 ◽  
Author(s):  
D. Chevallier ◽  
R. Douce ◽  
F. Nurit
Keyword(s):  
Cytochrome Oxidase ◽  
Dark Respiration ◽  
High Light ◽  
Light Conditions ◽  
Oxygen Production ◽  
Low Light ◽  
Funaria Hygrometrica ◽  
Light Intensities

The effect of DBMIB, antimycine A, and FCCP on respiration and photosynthesis of intact chlorophyllic moss (Funaria hygrometrica) spore was investigated.Antimycine A (1 μM) strongly inhibited dark respiration, was without effect on photosynthesis at high light intensities (above the saturation plateau values), and stimulated photosynthesis at low light intensities (below the saturation plateau values).DBMIB (3 μM) inhibited photosynthesis and was without effect, even under light conditions, on the dark respiration. Low amount of FCCP (3 μM) partially inhibited oxygen production at high light intensities. In this case, the inhibition observed was partially relieved by 1 μM antimycine A or 30 μM of KCN; higher concentration of FCCP totally inhibited the oxygen production.It seems likely, therefore, that in the chlorophyllic moss spore the cytochrome oxidase pathway is not functioning under high light intensities and that this inhibition of respiration is attributable to the low cytoplasmic ADP:ATP ratio.

Effect of Monochromatic Green LED Light Stimuli During Incubation on Embryo Growth, Hatching Performance, and Hormone Levels

2018 ◽  
Vol 61 (2) ◽  
pp. 661-669 ◽  
Author(s):  
Yue Yu ◽  
Zhanming Li ◽  
Zhengtao Zhong ◽  
Shufang Jin ◽  
Jinming Pan ◽  
...  
Keyword(s):  
Light Intensity ◽  
Green Light ◽  
Light Treatment ◽  
High Light ◽  
Low Light ◽  
Dark Treatment ◽  
Led Light ◽  
Green Led ◽  
Serum Hormone ◽  
Light Stimuli

Abstract. Previous research indicated improvement of incubation by light stimuli. However, the light source arrangement, usually with irradiation from top to bottom, was inconvenient and high in cost. Among the different light colors, the effects of green LED light stimuli during embryo development were inconclusive. In this study, two LED lamps were installed on both sides of egg trays, and the irradiation was directed from the edges to the middle. The effect of green LED light with various light intensities was investigated. A total of 1408 broiler eggs were randomly allocated to high light (300 lx), middle light (150 lx), low light (50 lx), and dark treatments with four replicates. Embryo weight, body length, organ weight, hatching performance, and serum hormone levels were tested. The results indicated that incubation of the broiler eggs under an appropriate light intensity (low light treatment, 50 lx) of green light significantly increased embryo weight, body length, and hatchability (p &lt; 0.001). According to the serum hormone tests, only the low light treatment significantly increased the thyroxine (T4) levels of the chicks (p &lt; 0.05) at hatching, but the middle and high light treatments slightly decreased the T4 and testosterone (TES) levels of the chicks compared with the dark treatment. Moreover, peak hatching time occurred 12 h earlier in the light treatments compared with the dark treatment. In conclusion, an appropriate light intensity (low light treatment, 50 lx) of LED green light improved embryo growth and hatching performance, but excessive light intensity reduced the positive effects or even produced slight negative effects on the T4 and TES levels of chicks at hatching. Keywords: Embryo, Growth, Hatching performance, Hormone, Monochrome green light.

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