Abstract:The tolerance to low water availability is a decisive factor for growth and survival of orchids in their natural environment. The objective of this study was to characterize the photochemical traits of two epiphytic orchids (Cattleya warneri and Miltonia spectabilis) under water deficit (WD). Chlorophyll a fluorescence signals were recorded from young and fully expanded leaves of 5 plants/species after dark-adaption for 60 minutes, between 6-9 a.m. after 0, 30, 60, and 90 days of WD, using a Handy-PEA fluorome… Show more
“…In addition, there was a significant discrepancy in the Mo, V J , and Sm values (P < 0.01) seen among M. aeruginosa cells cultivated at varying doses of Z. bungeanum residue extracts (Fig. 7 C–E), and the increase in Mo, V J, and Sm values indicated the limited electron flux beyond Q A , resulting in a blockade of electron transport of PSII 41 . Figure 7 Z. bungeanum residue extracts inhibited the electron transport of PSII.…”
Water eutrophication has emerged as a pressing concern for massive algal blooms, and these harmful blooms can potentially generate harmful toxins, which can detrimentally impact the aquatic environment and human health. Consequently, it is imperative to identify a safe and efficient approach to combat algal blooms to safeguard the ecological safety of water. This study aimed to investigate the procedure for extracting total flavonoids from Z. bungeanum residue and assess its antioxidant properties. The most favorable parameters for extracting total flavonoids from Z. bungeanum residue were a liquid–solid ratio (LSR) of 20 mL/g, a solvent concentration of 60%, an extraction period of 55 min, and an ultrasonic temperature of 80 °C. Meanwhile, the photosynthetic inhibitory mechanism of Z. bungeanum residue extracts against M. aeruginosa was assessed with a particular focus on the concentration-dependent toxicity effect. Z. bungeanum residue extracts damaged the oxygen-evolving complex structure, influenced energy capture and distribution, and inhibited the electron transport of PSII in M. aeruginosa. Furthermore, the enhanced capacity for ROS detoxification enables treated cells to sustain their photosynthetic activity. The findings of this study hold considerable relevance for the ecological management community and offer potential avenues for the practical utilization of resources in controlling algal blooms.
“…In addition, there was a significant discrepancy in the Mo, V J , and Sm values (P < 0.01) seen among M. aeruginosa cells cultivated at varying doses of Z. bungeanum residue extracts (Fig. 7 C–E), and the increase in Mo, V J, and Sm values indicated the limited electron flux beyond Q A , resulting in a blockade of electron transport of PSII 41 . Figure 7 Z. bungeanum residue extracts inhibited the electron transport of PSII.…”
Water eutrophication has emerged as a pressing concern for massive algal blooms, and these harmful blooms can potentially generate harmful toxins, which can detrimentally impact the aquatic environment and human health. Consequently, it is imperative to identify a safe and efficient approach to combat algal blooms to safeguard the ecological safety of water. This study aimed to investigate the procedure for extracting total flavonoids from Z. bungeanum residue and assess its antioxidant properties. The most favorable parameters for extracting total flavonoids from Z. bungeanum residue were a liquid–solid ratio (LSR) of 20 mL/g, a solvent concentration of 60%, an extraction period of 55 min, and an ultrasonic temperature of 80 °C. Meanwhile, the photosynthetic inhibitory mechanism of Z. bungeanum residue extracts against M. aeruginosa was assessed with a particular focus on the concentration-dependent toxicity effect. Z. bungeanum residue extracts damaged the oxygen-evolving complex structure, influenced energy capture and distribution, and inhibited the electron transport of PSII in M. aeruginosa. Furthermore, the enhanced capacity for ROS detoxification enables treated cells to sustain their photosynthetic activity. The findings of this study hold considerable relevance for the ecological management community and offer potential avenues for the practical utilization of resources in controlling algal blooms.
“…6 a–c). The increase in Vk and Vj are indication of limited electron flux resulting from the accumulation of PSII acceptors (QA and QB, the primary and secondary electron acceptors of PSII, respectively) and the plastoquinone (PQ) pool, leading to a blockade of electron transport (Zampirollo et al 2021 ). Notably, R light exposure resulted in a significant increase in the Vk and Vj or ΔVk and ΔVj, confirming the negative effect of R light on photosynthetic units on the 7th and 21st day (Fig.…”
Different light spectra from light-emitting diodes (LEDs) trigger species-specific adaptive responses in plants. We exposed
Artemisia argyi
(
A. argyi
) to four LED spectra: white (the control group), monochromatic red light (R), monochromatic blue light (B), or a mixture of R and B light of photon flux density ratio is 3 (RB), with equivalent photoperiod (14 h) and light intensity (160 μmol s
−1
m
−2
). R light accelerated photomorphogenesis but decreased biomass, while B light significantly increased leaf area and short-term exposure (7 days) to B light increased total phenols and flavonoids. HPLC identified chlorogenic acid, 3,5-dicaffeoylquinic acid, gallic acid, jaceosidin, eupatilin, and taxol compounds, with RB and R light significantly accumulating chlorogenic acid, 3,5-dicaffeoylquinic acid, and gallic acid, and B light promoting jaceosidin, eupatilin, and taxol. OJIP measurements showed that B light had the least effect on the effective quantum yield ΦPSII, with higher rETR(II), Fv/Fm, qL and PIabs, followed by RB light. R light led to faster photomorphology but lower biomass than RB and B lights and produced the most inadaptability, as shown by reduced ΦPSII and enlarged ΦNPQ and ΦNO. Overall, short-term B light promoted secondary metabolite production while maintaining effective quantum yield and less energy dissipation.
“…The ability of shade-loving plants to respond to changes in their light environment, e.g., dynamic events of opening and closing of forest clearings, has a significant repercussion on their performance, being critical and decisive in the competition for natural resources (Craine and Dybzinski, 2013). Therefore, higher photosynthetic efficiency is observed in orchids that grow under low luminosity (Zampirollo et al, 2021). On the other hand, high-light irradiation reduces photosynthetic efficiency due to photoinhibition of them (Wu et al, 2020).…”
In order to establish a link between the evolutionary history and the photochemical attributes, measurements of chlorophyll (Chl) a fluorescence were made in Cattleya warneri, C. shofieldiana and C. harrisoniana exposed to high irradiance for 5, 35, and 120 min (hereafter referred to as treatments T5, T35, and T120, respectively). The following questions are addressed: (1) Is the increased energy dissipation enough to counterbalance the excess energy that drives photosynthesis at different times of high irradiance exposure? (2) Is there an influence of the incidence and duration of light radiation on Cattleya species in full sunlight, compared to Cattleya species submitted to low irradiance? Higher relative variable fluorescence at the J-step (Vj) values followed by the lower quantum yield of electron transport (ψEo) indicate the accumulation of reduced Quinone A (QA) proportionally of sunflecks exposure time in C. warneri. The higher performance index (PIABS) and plasticity index values in C. schofieldiana indicate higher efficiency in modulating the photosynthetic apparatus under sunflecks. C. harrisoniana shows the lowest plasticity index, suppression of maximum fluorescence (Fm), and no recovery of PIABS after sunflecks. This study evidences the importance of physiological plasticity in the current geographic distribution of Cattleya in response to light pulses in species derived from fragmented habitats and the maintenance of shade to species of more primitive clades.
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