Relevant bibliographies by topics / Plant response to light

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Plant response to light'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Plant response to light"

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Omasa, Kenji. "Plant Response to Light." JOURNAL OF THE ILLUMINATING ENGINEERING INSTITUTE OF JAPAN 77, Appendix (1993): 191–92. http://dx.doi.org/10.2150/jieij1980.77.appendix_191.

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Rajapakse, Nihal C., Robert K. Pollock, Margaret J. McMahon, John W. Kelly, and Roy E. Young. "Interpretation of Light Quality Measurements and Plant Response in Spectral Filter Research." HortScience 27, no. 11 (November 1992): 1208–11. http://dx.doi.org/10.21273/hortsci.27.11.1208.

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Experiments were conducted to correlate the response of chrysanthemum [Dendrathema ×grandiflorum (Ramat.) Kitamura] plants to light environment based on various quantitative light quality parameters by growing plants under 6% or 40% CuSO4 and water spectral filters. Using a narrow band width (R = 655-665 and FR = 725-735 nm) or a broad band width (R = 600-700 and FR = 700-800 nm) for R: FR ratio calculation, 6% CuSO4 filter transmitted light with a higher R: FR ratio than 40% CuSO4 or water filters. Light transmitted through 40% CuSO4 and water filters had similar narrow band R: FR ratios (≈1.2), but the broad band R: FR ratio (2.0) of 40% CuSO4 filter was higher than that of water filters. The estimated phytochrome photoequilibrium (ϕ) value varied considerably with the photochemical properties of phytochrome used for estimations. Final height and internode length of plants grown in 6% or 40% CuSO4 chambers was ≈30% less than of plants in corresponding control chambers. Leaf and stem dry weights were reduced by light transmitted through CuSO4 filters. The results suggest that broad band R: FR ratio correlated more closely to above plant responses than the narrow band R: FR ratio. Blue (B): R and B: FR ratios (not absolute amount of blue wavelengths) correlated well with plant response, suggesting that involvement of blue light should not be ignored in expressing plant response to light transmitted through CuSO4 filters. At present, the presentation of complete spectral data would be the most useful in explaining plant response to light environment.
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Spetea, Cornelia, Eevi Rintamäki, and Benoît Schoefs. "Changing the light environment: chloroplast signalling and response mechanisms." Philosophical Transactions of the Royal Society B: Biological Sciences 369, no. 1640 (April 19, 2014): 20130220. http://dx.doi.org/10.1098/rstb.2013.0220.

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Light is an essential environmental factor required for photosynthesis, but it also mediates signals to control plant development and growth and induces stress tolerance. The photosynthetic organelle (chloroplast) is a key component in the signalling and response network in plants. This theme issue of Philosophical Transactions of the Royal Society of London B: Biology provides updates, highlights and summaries of the most recent findings on chloroplast-initiated signalling cascades and responses to environmental changes, including light and biotic stress. Besides plant molecular cell biology and physiology, the theme issue includes aspects from the cross-disciplinary fields of environmental adaptation, ecology and agronomy.
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Agrawal, Shashi Bhushan, and Deepanshi Jaiswal. "Impact of Light Stress on Plant Based Medicinally Active Compounds." INTERNATIONAL JOURNAL OF PLANT AND ENVIRONMENT 4, no. 02 (July 31, 2018): 50–59. http://dx.doi.org/10.18811/ijpen.v4i02.6.

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Light has several positive and negative impacts on plant growth and physiological processes. Medicinal plants contribute significantly higher proportions of world plant flora and are natural source of rich medicinal compounds. Sufficient literature is available on plant responses to light stress but studies on medicinal plants are limited. This review discusses how different light conditions affect production of plant-based medicinal compounds which are broadly secondary products formed during adverse environmental conditions to cope up the stress. Here, some medicinal plants are reviewed which were exposed to different light conditions including blue light, red light, yellow light, green light, far red light, wavelength specific light treatments, pulsed pre light, specific light intensity, light shade treatments, and supplemental ultraviolet-B radiation. Secondary metabolites considered for the review are anthocyanin, flavonoids, alkaloids, essential oils, cannabinoids and glucosinolates. Most of the results revealed increase in content of medicinal compounds under differentially exposed light conditions with maximum effect under sUV-B exposure. Advancement in the knowledge of medicinal plants response to light stress can help in understanding the mechanism of medicinal compound formation and their regulation which can be further utilized in the production of medicinally active compounds.
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Green-Tracewicz, Emily, Eric R. Page, and Clarence J. Swanton. "Shade Avoidance in Soybean Reduces Branching and Increases Plant-to-Plant Variability in Biomass and Yield Per Plant." Weed Science 59, no. 1 (March 2011): 43–49. http://dx.doi.org/10.1614/ws-d-10-00081.1.

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Recent studies have suggested that soybeans express shade avoidance in response to low red : far-red (R : FR) light reflected from neighboring plants and that this response may determine the onset and outcome of crop–weed competition. We tested the hypothesis that the low R : FR ratio would trigger characteristic shade avoidance responses in soybean and that the subsequent phenotype would experience reproductive costs under non–resource-limiting conditions. Soybeans were grown in a fertigation system in field trials conducted in 2007 and 2008 under two light quality treatments: (1) high R : FR ratio (i.e., weed-free) i.e., upward reflected light from a baked clay medium (Turface MVP®), or (2) low R : FR ratio (i.e., weedy) of upward reflected light, from commercial turfgrass. Results of this study indicated that a reduction in the R : FR ratio of light reflected from the surface of turfgrass increased soybean internode elongation, reduced branching, and decreased yield per plant. Shade avoidance also increased the plant-to-plant variability in biomass and yield per plant. Per plant yield losses were, however, more closely associated with reductions in biomass accumulation than population variability as the expression of a shade avoidance response did not influence harvest index. While these results suggest that weed induced shade avoidance decreases soybean per plant yield by reducing branching, it is possible the productivity of a soybean stand as a whole may be buffered against these reduction by a similar, but opposite, expression of plasticity in branching.
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Orzechowska, A., M. Trtílek, and E. Niewiadomska. "Thermographic Study of Plant Response to Excessive Light." Acta Physica Polonica A 139, no. 3 (March 2021): 257–60. http://dx.doi.org/10.12693/aphyspola.139.257.

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Scuderi, Domenica, Francesco Giuffrida, Stefania Toscano, and Daniela Romano. "Growth, Physiological Response, and Quality Characteristics of Weeping Fig in Response to Shading Levels and Climatic Conditions." HortScience 47, no. 11 (November 2012): 1586–92. http://dx.doi.org/10.21273/hortsci.47.11.1586.

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The aim of this study was to evaluate the effects of light availability and the climatic conditions on the growth and quality of weeping fig (Ficus benjamina L.). Plants of cv. Danielle were grown under five shading conditions (0%, 20%, 40%, 60%, and 80% reduction of the incident irradiance inside the greenhouse) and two cultivation periods (from May to October and from December to May). The light intensity in no shading treatment ranged from 6.3 to 16.4 MJ·m−2·d−1 in May to October and from 4.6 to 14.5 MJ·m−2·d−1 in December to May. Depending on climatic conditions, the light reduction resulting from shading produced strong differences in the growth of weeping fig. With increasing shading, the dry weight decreased from 282.4 to 113.3 g/plant during the first growth period, which was the period characterized by the highest values of global radiation and temperature, and from 120.8 to 56.8 g/plant during the second period. The effects of reduced light were evident in the plant quality, which is associated with the canopy and leaf characteristics. In particular, as a result of the increase of the apparent quantum yield and reduction of light compensation point, the most shaded plants showed a photosynthetic advantage over the control (0%) at a low irradiance level. Increased shading caused a reduction of plant compactness because of the increase of the internode length and branch insertion angle. Although shading also resulted in a reduction in the leaf number, the plant ornamental value was unaffected because of the highest unit leaf area (+72%) in both of the growth periods. Based on our results, the greatest decrease in irradiance (60% and 80% of shading) reduced the plant growth and compactness more in the growth period characterized by the highest values of global radiation and temperature, whereas the quality of the plants was improved by shading in both of the growth periods.
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Hatt, Heather, Arne Sæbø, and Dennis R. Decoteau. "PHOTOMORPHOGENIC DEVELOPMENT AND CARBOHYDRATE COMPOSITION OF YOUNG WATERMELON PLANTS AS AFFECTED BY INDIVIDUAL OR MULTIPLE FR SIGNALS DURING THE DARK PHASE OF THE PHOTOPERIOD." HortScience 27, no. 6 (June 1992): 641e—641. http://dx.doi.org/10.21273/hortsci.27.6.641e.

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Treatment of young watermelon (Citrullus lanatus cv. Sugar Baby) plants with individual and multiple FR light (15 min) treatments during the dark phase of the photoperiod influenced plant growth and development (i.e., petiole elongation, internode elongation, and reduced petiole angles) as compared to plants not treated with FR signals. The timing for the most effective light signal for inducing a growth response was when the signal was delivered immediately after the plant entered into the dark phase of the photoperiod. Decreasing growth responses to FR signals were observed as the signals were delayed after the plant entered into the dark phase. Multiple FR signals during the dark phase slightly increased growth responses as compared to plants that received the signal immediately after the light period. Young watermelon plant growth responses to FR light signals do not appear to be photoperiodic as plants similarly treated with a white light signal did not generate growth responses. Tissue analysis of petioles, leaves, stems, and cotyledons from plants treated with individual and multiple FR signals suggested that carbohydrate composition, distribution, and diurnal fluctuation were affected by the light quality treatments.
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Li, J., R. Z. Xie, K. R. Wang, P. Hou, B. Ming, G. Q. Zhang, G. Z. Liu, M. Wu, Z. S. Yang, and S. K. Li. "Response of canopy structure, light interception and grain yield to plant density in maize." Journal of Agricultural Science 156, no. 6 (August 2018): 785–94. http://dx.doi.org/10.1017/s0021859618000692.

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AbstractGood canopy structure is essential for optimal maize (Zea mays L.) production. However, creating appropriate maize canopy structure can be difficult, because the characteristics of individual plants are altered by changes in plant age, density and interactions with neighbouring plants. The objective of the current study was to find a reliable method for building good maize canopy structure by analysing changes in canopy structure, light distribution and grain yield (GY). A modern maize cultivar (ZhengDan958) was planted at 12 densities ranging from 1.5 to 18 plants/m2 at two field locations in Xinjiang, China. At the silking stage (R1), plant and ear height increased with plant density as well as leaf area index (LAI), whereas leaf area per plant decreased logarithmically. The fraction of light intercepted by the plant (F) increased with increasing plant density, but the light extinction coefficient (K) decreased linearly from 0.61 to 0.39. Taking the optimum value of F (95%) as an example, and using measured values of K for each plant density at R1 and the equation from Beer's law, the corresponding (theoretical) LAI for each plant density was calculated and optimum plant density (9.72 plants/m2) obtained by calculating the difference between theoretical LAIs and actual observations. Further analysis showed that plant density ranging from 10.64 to 11.55 plants/m2 yielded a stable GY range. Therefore, taking into account the persistence time for maximum LAI, the plant density required to obtain an ideal GY maize canopy structure should be increased by 10–18% from 9.72 plants/m2.
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Teixeira, Rita Teresa. "Distinct Responses to Light in Plants." Plants 9, no. 7 (July 15, 2020): 894. http://dx.doi.org/10.3390/plants9070894.

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The development of almost every living organism is, to some extent, regulated by light. When discussing light regulation on biological systems, one is referring to the sun that has long been positioned in the center of the solar system. Through light regulation, all life forms have evolved around the presence of the sun. As soon our planet started to develop an atmospheric shield against most of the detrimental solar UV rays, life invaded land, and in the presence of water, it thrived. Especially for plants, light (solar radiation) is the source of energy that controls a high number of developmental aspects of growth, a process called photomorphogenesis. Once hypocotyls reach soil′s surface, its elongation deaccelerates, and the photosynthetic apparatus is established for an autotrophic growth due to the presence of light. Plants can sense light intensities, light quality, light direction, and light duration through photoreceptors that accurately detect alterations in the spectral composition (UV-B to far-red) and are located throughout the plant. The most well-known mechanism promoted by light occurring on plants is photosynthesis, which converts light energy into carbohydrates. Plants also use light to signal the beginning/end of key developmental processes such as the transition to flowering and dormancy. These two processes are particularly important for plant´s yield, since transition to flowering reduces the duration of the vegetative stage, and for plants growing under temperate or boreal climates, dormancy leads to a complete growth arrest. Understanding how light affects these processes enables plant breeders to produce crops which are able to retard the transition to flowering and avoid dormancy, increasing the yield of the plant.
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Dissertations / Theses on the topic "Plant response to light"

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Schwalb, Michael. "Measuring the short term plant photosynthetic response to varying light quality using light emitting diodes (LEDs)." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=121207.

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Light emitting diodes (LEDs) emit narrow bandwidth light and have the potential to increase the spectral efficiency of supplemental lighting in greenhouses by optimizing spectral output for plant growth and yields. At the moment of writing, data describing the plant response to varying light quality and quantity was limited. The objective of this research was to examine photosynthetic response of plants to varying light quality and quantity and to gather photosynthetic response data that could be used to design an optimal spectrum for a prototype LED array for plant growth experiments. The action spectrum of tomato (Solanum lycopersicum), lettuce (Lactuca sativa) and petunia (Petunia × hybrida) seedlings was measured at three irradiances (30, 60 and 120 µmol m-2 sec-1) using LED arrays with peak wavelengths from 405nm – 700nm and a bandwidth of 25nm (full width at half maximum). The action spectrums for all plant species at all three irradiances were characterized by localized blue and red action peaks within the range of 430 to 449 nm and 624 to 660 nm respectively. A peak also occurred at 595 nm for 30 µmol m-2 sec-1. The photosynthetic response of tomato, lettuce and petunia to varying red (660nm) and blue (430nm) wavelengths with and without background broadband radiation was also measured. For all three species tested, with and without background radiation, the optimum photosynthesis range occurred within the red to blue ratio (r:b) range of 5:1- 15:1 except for petunia without background radiation for which the maximum occurred at 50:1. These results suggest that the optimal red to blue ratio for photosynthetic activity for tomato, lettuce and petunia occurred between a red to blue ratio of 5:1-15:1.
Les diodes électroluminescentes (DEL) émettent une lumière relativement monochromatique et pourraient accroître l'efficacité des lampes pour les serres commerciales en émettant des longueurs d'ondes optimisées pour le rendement des plantes. L'objectif de ce projet a consisté à examiner l'effet des longueurs d'ondes sur l'activité photosynthétique des plantes. L'activité photosynthétique des tomates (Solanum lycopersicum), laitues (Lactuca sativa) et pétunias (Petunia × hybrida) a été mesurée à trois puissances d'irradiation (30, 60 and 120 µmol m-2 sec-1) en utilisant des DELs avec une émission maximale entre 405 nm et 700 nm et une bande passante de 25 nm. La réponse photosynthétique maximale à chaque niveau d'irradiation se situait dans la portion bleu et rouge du spectre visible, soit respectivement entre 430 - 449 nm et 624 to 660 nm. Un maximum a aussi été observé à 595 nm à 30 µmol m-2 sec-1. L'effet de la proportion des longueurs d'onde bleue et rouge (émises par les DELs) sur l'activité photosynthétique des tomates, laitues et pétunias a aussi été mesuré avec et sans le rayonnement de fond. Pour chaque espèce, avec et sans le rayonnement de fond, la proportion optimale (en terme de rouge et bleu) pour l'activité photosynthétique se situait entre of 5:1- 15:1, sauf dans le cas du pétunia, pour lequel le maximum se situait à 50:1 sans rayonnement de fond. La proportion optimale pour l'activité photosynthétique a diminué avec le rayonnement de fond pour chaque espèce à chaque niveau d'irradiation.
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Choudhury, Feroza Kaneez. "Rapid Metabolic Response of Plants Exposed to Light Stress." Thesis, University of North Texas, 2018. https://digital.library.unt.edu/ark:/67531/metadc1157543/.

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Environmental stress conditions can drastically affect plant growth and productivity. In contrast to soil moisture or salinity that can gradually change over a period of days or weeks, changes in light intensity or temperature can occur very rapidly, sometimes over the course of minutes or seconds. So, in our study we have taken an metabolomics approach to identify the rapid response of plants to light stress. In the first part we have focused on the ultrafast (0-90 sec) metabolic response of local tissues to light stress and in the second part we analyzed the metabolic response associated with rapid systemic signaling (0-12 min). Analysis of the rapid response of Arabidopsis to light stress has revealed 111 metabolites that significantly alter in their level during the first 90 sec of light stress exposure. We further show that the levels of free and total glutathione accumulate rapidly during light stress in Arabidopsis and that the accumulation of total glutathione during light stress is dependent on an increase in nitric oxide (NO) levels. We further suggest that the increase in precursors for glutathione biosynthesis could be linked to alterations in photorespiration, and that phosphoenolpyruvate could represent a major energy and carbon source for rapid metabolic responses. Taken together, our analysis could be used as an initial road map for the identification of different pathways that could be used to augment the rapid response of plants to abiotic stress. In addition, it highlights the important role of glutathione in initial stage of light stress response. Light-induced rapid systemic signaling and systemic acquired acclimation (SAA) are thought to play an important role in the response of plants to different abiotic stresses. Although molecular and metabolic responses to light stress have been extensively studied in local leaves, and to a lesser degree in systemic leaves, very little is known about the metabolic responses that occur in the different tissues that connect the local to the systemic leaves. These could be important in defining the specificity of the systemic response as well as in supporting the propagation of different systemic signals, such as the reactive oxygen species (ROS) wave. Here we report that local application of light stress to one rosette leaf resulted in a metabolic response that encompassed local, systemic and transport tissues (tissues that connect the local and systemic tissues), demonstrating a high degree of physical and metabolic continuity between different tissues throughout the plant. We further show that the response of many of the systemically altered metabolites could be associated with the function of the ROS wave, and that the level of eight different metabolites is altered in a similar way in all tissues tested (local, systemic, and transport tissues). These compounds could define a core metabolic signature for light stress that propagates from the local to the systemic leaves. Taken together, our findings suggest that metabolic changes occurring in cells that connect the local and systemic tissues could play an important role in mediating rapid systemic signaling and systemic acquired acclimation to light stress.
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Brown, Jordan C. "Photoreceptor regulation of plant responses to light and carbon dioxide." Thesis, University of Sheffield, 2018. http://etheses.whiterose.ac.uk/21595/.

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The scarcity of fresh water resources has highlighted concerns about the high percentage used for agricultural purposes. The strain on freshwater could be alleviated by improving crop water use as this is the largest consuming factor. Stomata are microscopic pores on the leaf epidermis which plants use to regulate their gas exchange. Importantly, stomata are required to balance CO2 uptake with water loss, with, 1-10 mmol CO2 taken up per mole of water lost. This is achieved through a combination of altering the aperture of the stomatal pores and regulating the number of stomata that develop on the leaf surface. These changes occur in response to environmental cues and hormone signals (Casson and Hetherington, 2010). An overall genetic pathway of light-controlled stomatal development has advanced the understanding of the regulatory light signaling mechanism. However, it remains unknown how light signaling interacts with other environmental signals, such as that of CO2, to impact intrinsic developmental pathways. In this thesis I describe experiments that investigate, in vivo, the impact of photoreceptor signaling on CO2 signal response within the context of stomatal development and function. The final results chapter of this thesis discusses that phyB mutants have altered stomatal response to combined changes in light and CO2 concentrations. I was able to observe increased water use efficiency of phyB via control of stomatal number, size and aperture. Furthermore I was able to observe that phyB is important to sensing elevated CO2 in terms of stomatal aperture response. These results indicate a key role of phyB in light and CO2 signal integration to control stomatal development and response.
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Maai, Eri. "Factors inducing the chloroplast movement in C₄ plants underhigh light-stress conditions and effects of the response on photosynthesis." Doctoral thesis, Kyoto University, 2020. http://hdl.handle.net/2433/253468.

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京都大学
0048
新制・論文博士
博士(農学)
乙第13360号
論農博第2891号
新制||農||1080(附属図書館)
学位論文||R2||N5299(農学部図書室)
(主査)教授 中﨑 鉄也, 教授 白岩 立彦, 教授 土井 元章
学位規則第4条第2項該当
Doctor of Agricultural Science
Kyoto University
DGAM
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Li, Xiaochun. "Development and Light Response of Leaves of Metasequoia and Close Relatives." Fogler Library, University of Maine, 2004. http://www.library.umaine.edu/theses/pdf/LiX2004.pdf.

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Rasool, Brwa Mohammad Ali. "The influence of light and leaf antioxidant status on plant responses to aphids." Thesis, University of Leeds, 2015. http://etheses.whiterose.ac.uk/15443/.

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Cross-tolerance to environmental stresses results from the synergistic co-activation of defence pathways that cross biotic-abiotic stress boundaries. However, the signalling mechanisms that underpin such responses remain poorly characterised. The effects of an abiotic stress (high light; HL) on the responses of Arabidopsis thaliana and tobacco (Nicotiana tabacum) plants to a biotic stress (infestation by the green peach aphid, Myzus persicae) were therefore analysed. Particular focus was placed on the role of cellular redox state as a regulator of cross-tolerance phenomena and the identification of signalling pathways that underpin aphid resistance. Aphid fecundity was measured in a range of A. thaliana mutants that have defects in non-enzymatic antioxidants (ascorbate and glutathione), enzymatic antioxidants (catalase) or downstream kinase/phosphatase signalling cascades, and in transgenic tobacco lines that have either increased or decreased levels of ascorbate oxidase. A pre-treatment with HL increased the resistance of transgenic tobacco plants with low ascorbate oxidase to aphid infestation. In contrast, the A. thaliana ascorbate oxidase knockout mutants did not show the HL-dependent decrease in aphid infestation. Aphid fecundity was decreased on A. thaliana mutants that have altered antioxidant (ascorbate, glutathione, catalase) status, or that lack the gamma (γ) subunit of protein phosphatase (PP2A). A pre-treatment with HL increased the resistance of A. thaliana plants to aphid infestation in all of the genotypes, except for the cat2 mutants that lack the photorespiratory form of leaf catalase and glutathione defective mutants. Taken together these findings demonstrate that redox processes and oxidative signalling are important modulators of aphid resistance and the light-aphid interaction. Moreover, the analysis of aphid fecundity on these A. thaliana mutants, which also have different levels of leaf camalexin, suggests that the levels of this secondary metabolite alone do not influence aphid infestation. A transcriptome and metabolome profiling analysis of the responses of the different tobacco lines highlights the central role of cell wall modifications/signalling as key components in plant responses to aphid infestation.
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Goodman, Jill Lynn. "Photosynthetic Responses of Eelgrass (Zostera marina L) to Light and Sediment Sulfide in a Shallow Barrier Island Lagoon." W&M ScholarWorks, 1992. https://scholarworks.wm.edu/etd/1539617651.

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Niechayev, Nicholas Alexander. "The Environmental Productivity and Photosynthetic Light Response of Agave americana:A Potential Semi-Arid Biofuel Feedstock." Ohio University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1468518584.

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Arshad, Naheed. "The response of a baffled plate to plane waves, with light and heavy fluid loading." Thesis, Imperial College London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394279.

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Barnes, Charles. "Morphological Responses of Wheat (Triticum Aestivum L.) to Changes in Phytochrome Photoequilibria, Blue Light and Photoperiod." DigitalCommons@USU, 1990. https://digitalcommons.usu.edu/etd/4353.

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Wheat (triticum aestivum, L.) plants were exposed to three different levels of phytochrome photoequilibria (φ), two different photoperiods, end-of-day far-red radiation, two different levels of blue (400-500 nm) light, three levels of photosynthetic photon flux (PPF), and two types of high intensity discharge lamp types. Tillering was reduced by lowered φ, by reduced amounts on blue light and by end-of-day far-red. Main culm development was increased by lowered φ, by increased PPF, and was reduced by shortened photoperiod and by reduced blue light. Leaf length was increased by increased PPF, lowered φ, and reduced blue light but was not affected by photoperiod, end-of-day far-red or lamp type. Dry-mass accumulation increased under increasing PPF but was unaffected by other treatment in these experiments.
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Books on the topic "Plant response to light"

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Vergara, B. S. The flowering response of the rice plant to photoperiod: A review of the literature. 4th ed. Los Baños, Philippines: International Rice Research Institute, 1986.

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Light and plant responses: A study of plant photophysiology and the natural environment. London: E. Arnold, 1990.

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Tenhunen, John D., Fernando M. Catarino, Otto L. Lange, and Walter C. Oechel, eds. Plant Response to Stress. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-70868-8.

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Egamberdieva, Dilfuza, and Parvaiz Ahmad, eds. Plant Microbiome: Stress Response. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5514-0.

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Hart, J. W. Light and plant growth. London: Unwin Hyman, 1988.

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Hart, J. W. Light and plant growth. London: Unwin Hyman, 1987.

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Whitelam, Garry C., and Karen J. Halliday, eds. Light and Plant Development. Oxford, UK: Blackwell Publishing Ltd, 2007. http://dx.doi.org/10.1002/9780470988893.

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Hart, J. W. Light and Plant Growth. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-011-5996-8.

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International Conference on Plants and Environmental Pollution (2nd 2002 Lucknow, India). Plant response to environmental stress. Edited by Tripathi R. D, International Society of Environmental Botanists (Lucknow, India), and National Botanical Research Institute (India). Lucknow: International Book Distributing Co., 2006.

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Fraser, Ron S. S., ed. Recognition and Response in Plant-Virus Interactions. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74164-7.

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Book chapters on the topic "Plant response to light"

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Nunes, M. Antonieta, and M. Céu Matos. "Effect of light on gas exchange parameters of sun and shade adapted leaves of Ceratonia siliqua, Coffea arabica and Malus domestica." In Plant Response to Stress, 369–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-70868-8_22.

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Riemann, Michael. "Phenotyping of Light Response on JA-Defective Mutant in Rice." In Jasmonate in Plant Biology, 23–28. New York, NY: Springer US, 2019. http://dx.doi.org/10.1007/978-1-0716-0142-6_2.

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Cuozzo, Maria, Steve A. Kay, and Nam-Hai Chua. "Regulatory Circuits of Light-Responsive Genes." In Plant Gene Research, 131–53. Vienna: Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-6950-6_8.

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Coe, Robert A., and HsiangChun Lin. "Light-Response Curves in Land Plants." In Methods in Molecular Biology, 83–94. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7786-4_5.

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Berger, M., P. Maury, S. Guy, F. Mojayad, and C. Planchon. "Photochemical Response to Excess Light as Influenced by the Developmental History of the Plant." In Photosynthesis: from Light to Biosphere, 3369–72. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_792.

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Vandenbussche, F., B. Vancompernolle, and D. Van Der Straeten. "Blue light dependence of Arabidopsis seedling ethylene responses." In Advances in Plant Ethylene Research, 95–100. Dordrecht: Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6014-4_20.

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Chazdon, Robin L., Robert W. Pearcy, David W. Lee, and Ned Fetcher. "Photosynthetic Responses of Tropical Forest Plants to Contrasting Light Environments." In Tropical Forest Plant Ecophysiology, 5–55. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1163-8_1.

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Latała, Adam. "Photosynthetic Light-Response Curves in Marine Benthic Plants from the Thau Lagoon." In Photosynthesis: from Light to Biosphere, 4741–44. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_1110.

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Gutiérrez-Grijalva, Erick P., Liliana Santos-Zea, Dulce L. Ambriz-Pérez, Leticia X. López-Martínez, and J. Basilio Heredia. "Flavones and Flavonols: Bioactivities and Responses Under Light Stress in Herbs." In Plant Phenolics in Sustainable Agriculture, 91–115. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-4890-1_4.

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Baker, Neil R., Gui-ying Nie, and Milica Tomasevic. "Responses of photosynthetic light- use efficiency and chloroplast development on exposure of leaves to ozone." In Plant Responses to the Gaseous Environment, 219–38. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1294-9_12.

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Conference papers on the topic "Plant response to light"

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Devireddy, Amith. "Coordinated and rapid whole‐plant systemic stomatal responses to light stress." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1048269.

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Medvedeva, A. S., M. N. Danilova, N. V. Kudryakova, and V. V. Kuznetsov. "The role of cytokinin receptors in the regulation of the response of Arabidopsis thaliana to light stress." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-284.

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Wang, Zhao, William Hockaday, Joseph White, and Jon Thomas. "The Response of Plant Biomarker Lipids to Water Stress and Light Variables." In Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.2799.

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Cadorna, Charles Anthon. "Morpho-physiological Responses and Resource Use of Lactuca sativa L. Grown in Controlled Environment under Different Light Regimes." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1332433.

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Lo Frano, Rosa, and Giuseppe Forasassi. "Dynamic Response of a Nuclear Power Plant Subjected to External Accident Event." In 18th International Conference on Nuclear Engineering. ASMEDC, 2010. http://dx.doi.org/10.1115/icone18-29896.

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In recent times there is a renewed worldwide interest in the development and application of advanced nuclear power plants (NPPs). Decisions on the construction of several NPPs with evolutionary light water reactors have been made (e.g. EPR in Finland and France, AP1000 in China, etc.) and more are under consideration for licensing in several countries. Innovative NPPs are designed to be built with very broad siting conditions; therefore the safety aspects related to the external events might follow new scenarios and failure modes, different from those well known for the currently operated reactors. In this paper, the intent is evaluating the structural integrity of a nuclear containment system subjected to dynamic loadings due to a Design Base Earthquake and an aircraft impact (large size civilian jets or military aircrafts impact), which represent the two most relevant external accidents that should be considered and investigated as part of the basic design of a NPP in particular a III+ and IV Gens. In fact a suitable safety design of the NPP containment system (according to the international safety and design code guidelines, as NRC or IAEA ones), even if designed to meet other design goal, may represent a “built-in protection” to avoid or mitigate the effects of mentioned dynamic loadings. To the purpose a rather sophisticated numerical methodology, adopting finite element (FEM) approach, is employed for studying the overall dynamic behaviour of nuclear reactor and to determine the structural effects of the propagation of dynamic seismic as well as impulsive loads (containment structure response) up to the relevant nuclear components. Therefore representative three-dimensional FEM models of mentioned NPP containment and aircraft structures were set up, and used, in the performed analyses taking also into account the suitable materials behaviour and their related constitutive laws as well as the seismic excitation (determined according to the NRC rules). Moreover the performed analyses and the carried out response analyses of internal components, to both the ground motion and impact loads, were studied to check the considered NPP containment strength reserve in the case of the considered events. The obtained results seem to confirm the possibility to achieve an optimization of the NPP internal components.
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Liming, James K., David H. Johnson, and Andrew A. Dykes. "Probabilistic Safety Assessment Technology for Commercial Nuclear Power Plant Security Evaluation." In 12th International Conference on Nuclear Engineering. ASMEDC, 2004. http://dx.doi.org/10.1115/icone12-49027.

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Commercial nuclear power plant physical security has received much more intensive treatment and regulatory attention since September 11, 2001. In light of advancements made by the nuclear power industry in the field of probabilistic safety assessment (PSA) for its power plants over that last 30 years, and given the many examples of successful applications of risk-informed regulation at U. S. nuclear power plants during recent years, it may well be advisable to apply a “risk-informed” approach to security management at nuclear power plants from now into the future. In fact, plant PSAs developed in response to NRC Generic Letter 88-20 and related requirements are used to help define target sets of critical plant safety equipment in our current security exercises for the industry. With reasonable refinements, plant PSAs can be used to identify, analyze, and evaluate reasonable and prudent approaches to address security issues and associated defensive strategies at nuclear power plants. PSA is the ultimate scenario-based approach to risk assessment, and thus provides a most powerful tool in identifying and evaluating potential risk management decisions. This paper provides a summary of observations of factors that are influencing or could influence cost-effective or “cost-reasonable” security management decision-making in the current political environment, and provides recommendations for the application of PSA tools and techniques to the nuclear power plant operational safety response exercise (OSRE) process. The paper presents a proposed framework for nuclear power plant probabilistic terrorist risk assessment (PTRA) that applies these tools and techniques.
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Kindfuller, Vincent, Neil Todreas, Jacopo Buongiorno, Michael Golay, Arthur Birch, Thomas Isdanavich, Ron Thomas, and Harvey Stevens. "Overview of Security Plan for Offshore Floating Nuclear Plant." In 2016 24th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icone24-61029.

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A new Offshore Floating Nuclear Plant (OFNP) concept with high potential for attractive economics and an unprecedented level of safety is presented, along with an overview of work done in the area of security. The OFNP creatively combines state-of-the-art Light Water Reactors (LWRs) with floating platforms such as those used in offshore oil/gas operations, both of which are well-established technologies which can allow implementation on a time scale consistent with combating climate change in the near future. OFNP is a plant that can be entirely built within a floating platform in a shipyard, transferred to the site. OFNP eliminates earthquakes and tsunamis as accident precursors; its ocean-based passive safety systems eliminate the loss of ultimate heat sink accident by design. The defense of an OFNP poses new security opportunities and challenges compared to land-based plants. Such a plant can be more easily defended by virtue of the clear 360 degree lines of sight and the relative ease of identifying surface threats. Conversely the offshore plant is potentially vulnerable to underwater approaches by mini-submarines and divers. We investigate security considerations of the OFNP applicable to two potential plant options, an OFNP-300 with a 300 MWe reactor, and an OFNP-1100 with an 1100 MWe reactor. Three innovative security system approaches could be combined for the offshore plant. The first is a comprehensive detection system which integrates radar, sonar and unmanned vehicles for a long distance overview of the vicinity of the plant. The second approach is the use of passive physical barriers about 100 meters from the plant, which will force a fast-moving power boat to lose speed or stop at the barrier allowing the plant security force more time to respond. The third approach takes advantage of the offshore plant siting and the monthly or biweekly rotation of crew to reduce the total on-plant and onshore security force by using the off-duty security force on the plant as a reserve force. Through the use of these approaches, the OFNP-300 should be able to achieve a similar security cost (on a per Megawatt basis) as land-based plants of similar or somewhat larger power rating. Due to non-linear scaling of cost, the security cost of the OFNP-1100 has the potential to be reduced significantly compared to its land-based equivalents.
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Lutz, Robert J., and Robert P. Prior. "Comparison of Fukushima Response in the United States and Europe." In 2016 24th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icone24-60101.

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The accident at the three reactor units at Fukushima Daiichi showed weaknesses in the plant coping capability for beyond design basis accidents caused by extreme external events. The weaknesses included plant design features, accident management procedures and guidance, and offsite emergency response. As a result, significant changes to plant coping capability have been made to light water reactors worldwide to enhance the coping capabilities for beyond design basis accidents. However, the response in the United States has been significantly different from that in Europe in a number of ways. In the United States, the regulator and the industry convened separate expert panels to review the Fukushima accident and make recommendations for enhancements. On the regulatory side, a series of three Orders were issued and that required the implementation of certain enhancements (Mitigation strategies, hardened vents for certain BWRs, spent fuel pool level indication) to ensure adequate protection for the health and safety of the public. Other enhancements were subject to the “Backfit Rule” which requires that changes to regulatory requirements be shown to be cost beneficial using accepted methodologies. Simultaneously, the industry took independent steps to develop a diverse and flexible coping strategies (known as FLEX) and other enhancements. The focus in the United States was clearly on enhancements to guarantee continued core, containment and spent fuel pool cooling in the event of beyond design basis accidents, particularly those resulting from extreme external events. In Europe, the regulatory agencies ordered the development and completion of “Stress Tests” for each reactor site. These Stress Tests were focused on identifying the capability of the plant and its staff to respond to increasingly severe external events. The Stress Tests not only examined the ability to maintain core, containment and spent fuel pool cooling but also the ability to mitigate the consequences of accidents that progress to core damage (i.e., a severe accident). Regulatory requirements were then issued by the national regulators that addressed the weaknesses identified from the Stress Tests. While many of the enhancements to the plant coping capability were similar to those in the United States, significant hardware enhancements were also required to reduce the consequences of core damage accidents including hydrogen control and containment filtered venting. Finally, most European regulators also include severe accident management guidance (SAMG) as a regulatory requirement. In the United States, SAMG will be maintained as a voluntary industry commitment that is subject to regulatory oversight review.
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Albrecht, Kevin J., and Robert J. Braun. "Dynamic Modeling of SOFC Cogeneration Systems for Light Commercial Applications." In ASME 2014 12th International Conference on Fuel Cell Science, Engineering and Technology collocated with the ASME 2014 8th International Conference on Energy Sustainability. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/fuelcell2014-6403.

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One potentially attractive application of solid oxide fuel cells (SOFCs) is for combined heat and power (CHP) in light commercial buildings. An SOFC-based CHP system can be employed to efficiently serve building thermal and electric loads, thereby lowering utility bills and offering many distributed generation benefits. It is often desirable to operate SOFCs in a predominately base load manner from a hardware viewpoint. However, systems in practice will experience some load dynamics during their lifetime and furthermore, optimal economic dispatch of CHP systems frequently recommends a load-following strategy. Thus, the present work is motivated by the need to understand the dynamic response capabilities of SOFC-CHP systems. Part-load performance and dynamic load-following capabilities of a 24 kW planar SOFC system for light commercial applications was investigated through computational modeling. The SOFC and balance-of-plant component models were implemented in gPROMS modeling software. The modeling strategy of each system component and associated transients are discussed. A dynamic SOFC channel-level model, which has been verified against experimental cell data, was integrated with additional balance-of-plant (BOP) component models consisting of a fuel reformer, tail gas combustor, turbomachinery, heat exchangers, and bypass valves. The performance of the system at part-load operation displays increases in electrical efficiency and decreases in CHP efficiency, as well as a more uniform PEN temperature profile. Modeling comparisons between the responses of systems consisting of either dynamic or steady-state BOP component models are reported. A fully dynamic system-level model displays anodic fuel depletion effects and waste heat recovery transients not captured by the steady-state models. The dynamics influence the ability of an SOFC system to load follow indicating when thermal and electric storage may be necessary.
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KARLOVSKA, Amanda, Inga GRĪNFELDE, Ina ALSIŅA, Gints PRIEDĪTIS, and Daina ROZE. "PLANT REFLECTED SPECTRA DEPENDING ON BIOLOGICAL CHARACTERISTICS AND GROWTH CONDITIONS." In Rural Development 2015. Aleksandras Stulginskis University, 2015. http://dx.doi.org/10.15544/rd.2015.045.

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Sustainable and economically based forestry needs modern inventory and monitoring techniques. One of the most common technologies for identification of forest tree species and monitoring of forest growth conditions is the hyperspectral remote sensing. This technology gives an opportunity to economize human resources and time for data collecting and processing. The spectral behaviour of plant leaves depends on number of factors, including environmental background. The aim of this study was to assess the tree reflectance spectra in relation to the growth conditions to take into account potential differences for increasing precision of species identification in Latvian forests and for estimating of forest growth conditions. Remote sensing data were obtained using a specialized aircraft (Pilatus PC-6), which is equipped with a high-performance airborne VNIR pushbroom hyperspectral system (AisaEAGLE). The study area was flown at 1000 m altitude. Data was recorded in the 400–970 nm spectral range, spectral resolution was 3.3 nm, ground resolution 0.5 m. Data processing consisted of manually selecting trees with a recognizable tree crowns in the airborne images. Tree centres were adjusted by putting them in the accurate position according to the situation in aerial photography. All trees with a diameter at breast height DBH of more than 5 cm were measured and for each tree coordinates, its species, height, DBH, crown width and length were recorded. Differentially corrected Global Positioning System measurements were used to determine the position of each plot centre. Data from different hyperspectral bands were compared using ANOVA at confidence level 95 %. Four species: Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst), silver birch (Betula pendula Roth), and European aspen (Populus tremula L.) – were examined in distinct forest site types. The spectral response of studied species was 1) different between species and 2) different between site types within each species, correlating with soil fertility gradient and soil moisture gradient. Differences between species occurred most in the intensity of reflected electromagnetic radiation rather than distinctive locations of maximums or minimums in spectrum curve, and near infrared (NIR) region of spectrum showed more differences between species than visible light zone. Most informative wavebands for distinguishing differences between site types were 805 nm and 644 nm.
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Reports on the topic "Plant response to light"

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Banerjee, Dwaipayan, and Pooja Vasanth K. IIHS COVID-19 Response Plan. Indian Institute for Human Settlements, 2021. http://dx.doi.org/10.24943/c19rp01.2021.

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This document comprises the contingency plan created for IIHS for the implementation of measures to mitigate risks and ensure emergency response preparedness in light of COVID- 19. IIHS has followed guidelines from the World Health Organization (WHO), Indian Council of Medical Research (ICMR), Ministry of Home Affairs (MHA) and the State Government while formulating its COVID-19 response plan across all IIHS offices at Bengaluru, Chennai, Trichy, Delhi and Mumbai.
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Ronzhin, Anatoly. Silicon timing response to different laser light. Office of Scientific and Technical Information (OSTI), January 2017. http://dx.doi.org/10.2172/1395486.

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Cummings, Molly E. Biological Response to the Dynamic Spectral-Polarized Underwater Light Field. Fort Belvoir, VA: Defense Technical Information Center, January 2010. http://dx.doi.org/10.21236/ada541131.

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Cummings, Molly E., Samir Ahmed, Heidi Dierssen, Alexander Gilerson, William F. Gilly, George Kattawar, Brad Seibel, and James Sullivan. Biological Response to the Dynamic Spectral-Polarized Underwater Light Field. Fort Belvoir, VA: Defense Technical Information Center, September 2013. http://dx.doi.org/10.21236/ada598460.

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Cummings, Molly E. Biological Response to the Dynamic Spectral-Polarized Underwater Light Field. Fort Belvoir, VA: Defense Technical Information Center, September 2011. http://dx.doi.org/10.21236/ada557141.

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Owensby, C. E., P. I. Coyne, J. M. Ham, W. Parton, C. Rice, L. M. Auen, and N. Adam. Rangeland Plant response to elevated CO{sub 2}. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/373752.

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Owensby, C., P. Coyne, and L. Auen. Rangeland-plant response to elevated CO sub 2. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/6771488.

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Kirkham, M., E. Kanemasu, G. Harbers, D. Reed, Hong He, R. Theisen, T. Bolger, et al. Rangeland-plant response to elevated CO sub 2. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6807822.

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Jacobson, J., P. Irving, A. Kuja, J. Lee, D. Shriner, J. Troiano, S. Perrigan, and V. Cullinan. A collaborative effort to model plant response to acidic rain. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/5415201.

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Abbott, Andrew, Brittany Branch, Eric N. Brown, Carl A. Carlson, Bradford E. Clements, Joshua D. Coe, Dana M. Dattelbaum, et al. The Dynamic Response of Polymers Interrogated by 3rd Generation X-ray Light Sources. Office of Scientific and Technical Information (OSTI), September 2019. http://dx.doi.org/10.2172/1566083.

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