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Journal articles on the topic 'Plants Plant physiology. Plants Plants. Plantes'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

Gurner, Ryan. "Physiology of Woody Plants." Pacific Conservation Biology 4, no. 3 (1998): 272. http://dx.doi.org/10.1071/pc980272.

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Plant physiology is the scientific study of how plants grow and respond to environmental factors and cultural treatments in terms of their physiological processes and conditions. This book aims to explain how physiological processes (such as photosynthesis, respiration, transpiration, carbohydrate, nitrogen and mineral relations) are involved in the growth of woody plants and how they are affected by the environment, in addition to explaining the mechanisms of the processes themselves.

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2

Stavrinidou, Eleni, Roger Gabrielsson, Eliot Gomez, Xavier Crispin, Ove Nilsson, Daniel T. Simon, and Magnus Berggren. "Electronic plants." Science Advances 1, no. 10 (November 2015): e1501136. http://dx.doi.org/10.1126/sciadv.1501136.

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The roots, stems, leaves, and vascular circuitry of higher plants are responsible for conveying the chemical signals that regulate growth and functions. From a certain perspective, these features are analogous to the contacts, interconnections, devices, and wires of discrete and integrated electronic circuits. Although many attempts have been made to augment plant function with electroactive materials, plants’ “circuitry” has never been directly merged with electronics. We report analog and digital organic electronic circuits and devices manufactured in living plants. The four key components of a circuit have been achieved using the xylem, leaves, veins, and signals of the plant as the template and integral part of the circuit elements and functions. With integrated and distributed electronics in plants, one can envisage a range of applications including precision recording and regulation of physiology, energy harvesting from photosynthesis, and alternatives to genetic modification for plant optimization.

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3

Maurel, Christophe, Yann Boursiac, Doan-Trung Luu, Véronique Santoni, Zaigham Shahzad, and Lionel Verdoucq. "Aquaporins in Plants." Physiological Reviews 95, no. 4 (October 2015): 1321–58. http://dx.doi.org/10.1152/physrev.00008.2015.

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Aquaporins are membrane channels that facilitate the transport of water and small neutral molecules across biological membranes of most living organisms. In plants, aquaporins occur as multiple isoforms reflecting a high diversity of cellular localizations, transport selectivity, and regulation properties. Plant aquaporins are localized in the plasma membrane, endoplasmic reticulum, vacuoles, plastids and, in some species, in membrane compartments interacting with symbiotic organisms. Plant aquaporins can transport various physiological substrates in addition to water. Of particular relevance for plants is the transport of dissolved gases such as carbon dioxide and ammonia or metalloids such as boron and silicon. Structure-function studies are developed to address the molecular and cellular mechanisms of plant aquaporin gating and subcellular trafficking. Phosphorylation plays a central role in these two processes. These mechanisms allow aquaporin regulation in response to signaling intermediates such as cytosolic pH and calcium, and reactive oxygen species. Combined genetic and physiological approaches are now integrating this knowledge, showing that aquaporins play key roles in hydraulic regulation in roots and leaves, during drought but also in response to stimuli as diverse as flooding, nutrient availability, temperature, or light. A general hydraulic control of plant tissue expansion by aquaporins is emerging, and their role in key developmental processes (seed germination, emergence of lateral roots) has been established. Plants with genetically altered aquaporin functions are now tested for their ability to improve plant tolerance to stresses. In conclusion, research on aquaporins delineates ever expanding fields in plant integrative biology thereby establishing their crucial role in plants.

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4

Ford, Brian J. "Physiology of Woody Plants." Botanical Journal of the Linnean Society 153, no. 2 (February 2007): 243. http://dx.doi.org/10.1111/j.1095-8339.2006.00620.x.

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5

Chaffey, Nigel. "Physiology and behaviour of plants." Annals of Botany 102, no. 1 (July 2008): 141–42. http://dx.doi.org/10.1093/aob/mcn072.

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6

Noordally, Zeenat B., and Antony N. Dodd. "Plants signal the time." Biochemist 42, no. 2 (March 31, 2020): 28–31. http://dx.doi.org/10.1042/bio04202003.

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Plants are generally sessile photosynthetic autotrophs; they depend on light for their existence and cannot move to escape challenging environmental conditions. This means that the lives of plants are intimately linked to daily fluctuations in environmental conditions caused by the rotation of the Earth on its axis. As a result, circadian regulation has an incredibly pervasive influence upon plant physiology, metabolism and development. For example, around 30% of the transcriptome of the model plant Arabidopsis thaliana is circadian regulated. In plants, the circadian clock influences processes of crucial importance such as photosynthesis, opening of the stomatal pores that allow gas exchange with the atmosphere, plant growth rates and organ position. It also contributes to the seasonal regulation of flowering. Taken together, this means that the circadian clock influences plant traits that are crucial to agricultural food production.

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7

Weber, Gerd. "Plant biotechnology and transgenic plants." Journal of Plant Physiology 161, no. 10 (October 2004): 1187–88. http://dx.doi.org/10.1016/j.jplph.2004.05.004.

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8

Broadley, Martin R., Philip J. White, John P. Hammond, Ivan Zelko, and Alexander Lux. "Zinc in plants." New Phytologist 173, no. 4 (March 2007): 677–702. http://dx.doi.org/10.1111/j.1469-8137.2007.01996.x.

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9

Gómez-Ariza, Jorge, Sonia Campo, Mar Rufat, Montserrat Estopà, Joaquima Messeguer, Blanca San Segundo, and María Coca. "Sucrose-Mediated Priming of Plant Defense Responses and Broad-Spectrum Disease Resistance by Overexpression of the Maize Pathogenesis-Related PRms Protein in Rice Plants." Molecular Plant-Microbe Interactions® 20, no. 7 (July 2007): 832–42. http://dx.doi.org/10.1094/mpmi-20-7-0832.

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Expression of pathogenesis-related (PR) genes is part of the plant's natural defense response against pathogen attack. The PRms gene encodes a fungal-inducible PR protein from maize. Here, we demonstrate that expression of PRms in transgenic rice confers broad-spectrum protection against pathogens, including fungal (Magnaporthe oryzae, Fusarium verticillioides, and Helminthosporium oryzae) and bacterial (Erwinia chrysanthemi) pathogens. The PRms-mediated disease resistance in rice plants is associated with an enhanced capacity to express and activate the natural plant defense mechanisms. Thus, PRms rice plants display a basal level of expression of endogenous defense genes in the absence of the pathogen. PRms plants also exhibit stronger and quicker defense responses during pathogen infection. We also have found that sucrose accumulates at higher levels in leaves of PRms plants. Sucrose responsiveness of rice defense genes correlates with the pathogen-responsive priming of their expression in PRms rice plants. Moreover, pretreatment of rice plants with sucrose enhances resistance to M. oryzae infection. Together, these results support a sucrose-mediated priming of defense responses in PRms rice plants which results in broad-spectrum disease resistance.

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10

Ayres, Peter. "The physiology of plants under stress." Physiological and Molecular Plant Pathology 36, no. 4 (April 1990): 361–62. http://dx.doi.org/10.1016/0885-5765(90)90065-6.

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11

Chagué, Véronique, Levanoni-Visel Danit, Verena Siewers, Christian Schulze Gronover, Paul Tudzynski, Bettina Tudzynski, and Amir Sharon. "Ethylene Sensing and Gene Activation in Botrytis cinerea: A Missing Link in Ethylene Regulation of Fungus-Plant Interactions?" Molecular Plant-Microbe Interactions® 19, no. 1 (January 2006): 33–42. http://dx.doi.org/10.1094/mpmi-19-0033.

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Ethylene production by infected plants is an early resistance response leading to activation of plant defense pathways. However, plant pathogens also are capable of producing ethylene, and ethylene might have an effect not only on the plant but on the pathogen as well. Therefore, ethylene may play a dual role in fungus—plant interactions by affecting the plant as well as the pathogen. To address this question, we studied the effects of ethylene on the gray mold fungus Botrytis cinerea and the disease it causes on Nicotiana benthamiana plants. Exposure of B. cinerea to ethylene inhibited mycelium growth in vitro and caused transcriptional changes in a large number of fungal genes. A screen of fungal signaling mutants revealed a Gα null mutant (Δbcg1) which was ethylene insensitive, overproduced ethylene in vitro, and showed considerable transcriptional changes in response to ethylene compared with the wild type. Aminoethoxyvinylglycine (AVG)-treated, ethylene-nonproducing N. benthamiana plants developed much larger necroses than ethylene-producing plants, whereas addition of ethylene to AVG-treated leaves restricted disease spreading. Ethylene also affected fungal gene expression in planta. Expression of a putative pathogenicity fungal gene, bcspl1, was enhanced 24 h after inoculation in ethylene-producing plants but only 48 h after inoculation in ethylene-nonproducing plants. Our results show that the responses of B. cinerea to ethylene are partly mediated by a G protein signaling pathway, and that ethylene-induced plant resistance might involve effects of plant ethylene on both the plant and the fungus.

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12

Tester, Mark, and Antony Bacic. "Abiotic Stress Tolerance in Grasses. From Model Plants to Crop Plants." Plant Physiology 137, no. 3 (March 2005): 791–93. http://dx.doi.org/10.1104/pp.104.900138.

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13

Dumon, J. C., and W. H. O. Ernst. "Titanium in Plants." Journal of Plant Physiology 133, no. 2 (September 1988): 203–9. http://dx.doi.org/10.1016/s0176-1617(88)80138-x.

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14

Posmyk, Małgorzata M., and Krystyna M. Janas. "Melatonin in plants." Acta Physiologiae Plantarum 31, no. 1 (September 13, 2008): 1–11. http://dx.doi.org/10.1007/s11738-008-0213-z.

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15

Eisenach, Cornelia, and Frederick C. Meinzer. "Hydraulics of woody plants." Plant, Cell & Environment 43, no. 3 (February 24, 2020): 529–31. http://dx.doi.org/10.1111/pce.13715.

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16

Fleming, Andrew J. "Producing patterns in plants." New Phytologist 170, no. 4 (June 2006): 639–41. http://dx.doi.org/10.1111/j.1469-8137.2006.01758.x.

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17

Johannes, Frank, and Robert J. Schmitz. "Spontaneous epimutations in plants." New Phytologist 221, no. 3 (September 14, 2018): 1253–59. http://dx.doi.org/10.1111/nph.15434.

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18

Kirchhoff, Helmut. "Chloroplast ultrastructure in plants." New Phytologist 223, no. 2 (March 8, 2019): 565–74. http://dx.doi.org/10.1111/nph.15730.

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19

Rillig, Matthias C., Anika Lehmann, A. Abel Souza Machado, and Gaowen Yang. "Microplastic effects on plants." New Phytologist 223, no. 3 (March 29, 2019): 1066–70. http://dx.doi.org/10.1111/nph.15794.

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20

Willis, Arthur J. "Endangered plants in Iran." New Phytologist 149, no. 2 (February 2001): 165. http://dx.doi.org/10.1046/j.1469-8137.2001.00043-3.x.

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21

JONES, RUSSELL L., and DAVID G. ROBINSON. "Protein secretion in plants." New Phytologist 111, no. 4 (April 1989): 567–97. http://dx.doi.org/10.1111/j.1469-8137.1989.tb02352.x.

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22

Etherington, J. R., M. G. Hale, and D. M. Orcutt. "The Physiology of Plants Under Stress." Journal of Ecology 76, no. 4 (December 1988): 1247. http://dx.doi.org/10.2307/2260647.

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23

Souza, Gustavo M., Tony Trewavas, and Danilo de Menezes Daloso. "Systems plant physiology: An integrated view of plants life." Progress in Biophysics and Molecular Biology 146 (September 2019): 1–2. http://dx.doi.org/10.1016/j.pbiomolbio.2019.06.005.

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24

Demeter, S., and Govindjee. "Thermoluminescence in plants." Physiologia Plantarum 75, no. 1 (January 1989): 121–30. http://dx.doi.org/10.1111/j.1399-3054.1989.tb02073.x.

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25

Robinson, David G., and Stefan Milliner. "Endocytosis in plants." Physiologia Plantarum 79, no. 1 (May 1990): 96–104. http://dx.doi.org/10.1111/j.1399-3054.1990.tb05871.x.

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26

De Cuyper, Carolien, and Sofie Goormachtig. "Strigolactones in the Rhizosphere: Friend or Foe?" Molecular Plant-Microbe Interactions® 30, no. 9 (September 2017): 683–90. http://dx.doi.org/10.1094/mpmi-02-17-0051-cr.

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Strigolactones are well-known endogenous plant hormones that play a major role in planta by influencing different physiological processes. Moreover, ex planta, strigolactones are important signaling molecules in root exudates and function as host detection cues to launch mutualistic interactions with arbuscular mycorrhizal fungi in the rhizosphere. However, parasitic plants belonging to the Orobanchaceae family hijacked this communication system to stimulate their seed germination when in close proximity to the roots of a suitable host. As a result, the secretion of strigolactones by the plant can have both favorable and detrimental outcomes. Here, we discuss these dual positive and negative effects of strigolactones and we provide a detailed overview on the role of these molecules in the complex dialogs between plants and different organisms in the rhizosphere.

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27

Kay, Elisabeth, Gaëlle Chabrillat, Timothy M. Vogel, and Pascal Simonet. "Intergeneric Transfer of Chromosomal and Conjugative Plasmid Genes Between Ralstonia solanacearum and Acinetobacter sp. BD413." Molecular Plant-Microbe Interactions® 16, no. 1 (January 2003): 74–82. http://dx.doi.org/10.1094/mpmi.2003.16.1.74.

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Conjugative transfer of a broad-host range plasmid and transformation-mediated transfer of chromosomal genes were found to occur at significant frequencies between Ralstonia solanacearum and Acinetobacter sp. in planta. These intergeneric gene transfers are related to the conditions provided by the infected plant, including the extensive multiplication of these two bacteria in planta and the development of a competence state in Acinetobacter sp. Although interkingdom DNA transfer from nuclear transgenic plants to these bacteria was not detectable, plants infected by pathogens (e.g., Ralstonia solanacearum) and co-colonized by soil saprophyte bacteria (e.g., Acinetobacter sp.) can be considered as potential “hot spots” for gene transfer, even between phylogenetically remote organisms.

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28

Bedhomme, Mariette, Stefan Jouannic, Antony Champion, Viesturs Simanis, and Yves Henry. "Plants, MEN and SIN." Plant Physiology and Biochemistry 46, no. 1 (January 2008): 1–10. http://dx.doi.org/10.1016/j.plaphy.2007.10.010.

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29

Witte, Claus-Peter, and Marco Herde. "Nucleotide Metabolism in Plants." Plant Physiology 182, no. 1 (October 22, 2019): 63–78. http://dx.doi.org/10.1104/pp.19.00955.

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30

Miginiac-Maslow, Myroslawa, Bob B. Buchanan, and Jean Vidal. "Metabolic networks in plants." Plant Physiology and Biochemistry 41, no. 6-7 (June 2003): 503. http://dx.doi.org/10.1016/s0981-9428(03)00102-5.

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31

Grennan, Aleel K. "Lipid Rafts in Plants." Plant Physiology 143, no. 3 (March 2007): 1083–85. http://dx.doi.org/10.1104/pp.104.900218.

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32

Conn, Simon, and Matthew Gilliham. "Comparative physiology of elemental distributions in plants." Annals of Botany 105, no. 7 (April 21, 2010): 1081–102. http://dx.doi.org/10.1093/aob/mcq027.

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33

Loreti, Elena, and Pierdomenico Perata. "The Many Facets of Hypoxia in Plants." Plants 9, no. 6 (June 12, 2020): 745. http://dx.doi.org/10.3390/plants9060745.

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Plants are aerobic organisms that require oxygen for their respiration. Hypoxia arises due to the insufficient availability of oxygen, and is sensed by plants, which adapt their growth and metabolism accordingly. Plant hypoxia can occur as a result of excessive rain and soil waterlogging, thus constraining plant growth. Increasing research on hypoxia has led to the discovery of the mechanisms that enable rice to be productive even when partly submerged. The identification of Ethylene Response Factors (ERFs) as the transcription factors that enable rice to survive submergence has paved the way to the discovery of oxygen sensing in plants. This, in turn has extended the study of hypoxia to plant development and plant–microbe interaction. In this review, we highlight the many facets of plant hypoxia, encompassing stress physiology, developmental biology and plant pathology.

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34

Webb, Alex A. R. "The physiology of circadian rhythms in plants." New Phytologist 160, no. 2 (November 2003): 281–303. http://dx.doi.org/10.1046/j.1469-8137.2003.00895.x.

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35

Hedrich, Rainer. "Ion Channels in Plants." Physiological Reviews 92, no. 4 (October 2012): 1777–811. http://dx.doi.org/10.1152/physrev.00038.2011.

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Since the first recordings of single potassium channel activities in the plasma membrane of guard cells more than 25 years ago, patch-clamp studies discovered a variety of ion channels in all cell types and plant species under inspection. Their properties differed in a cell type- and cell membrane-dependent manner. Guard cells, for which the existence of plant potassium channels was initially documented, advanced to a versatile model system for studying plant ion channel structure, function, and physiology. Interestingly, one of the first identified potassium-channel genes encoding the Shaker-type channel KAT1 was shown to be highly expressed in guard cells. KAT1-type channels from Arabidopsis thaliana and its homologs from other species were found to encode the K+-selective inward rectifiers that had already been recorded in early patch-clamp studies with guard cells. Within the genome era, additional Arabidopsis Shaker-type channels appeared. All nine members of the Arabidopsis Shaker family are localized at the plasma membrane, where they either operate as inward rectifiers, outward rectifiers, weak voltage-dependent channels, or electrically silent, but modulatory subunits. The vacuole membrane, in contrast, harbors a set of two-pore K+ channels. Just very recently, two plant anion channel families of the SLAC/SLAH and ALMT/QUAC type were identified. SLAC1/SLAH3 and QUAC1 are expressed in guard cells and mediate Slow- and Rapid-type anion currents, respectively, that are involved in volume and turgor regulation. Anion channels in guard cells and other plant cells are key targets within often complex signaling networks. Here, the present knowledge is reviewed for the plant ion channel biology. Special emphasis is drawn to the molecular mechanisms of channel regulation, in the context of model systems and in the light of evolution.

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36

DeMeo, Robin A., and Thomas E. Marler. "Growth, Morphology, and Physiology of Intsia bijuga Trees Under Varied Light Conditions." HortScience 33, no. 3 (June 1998): 480c—480. http://dx.doi.org/10.21273/hortsci.33.3.480c.

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Six studies were conducted with Intsia bijuga seedlings to determine the methods and extent of shade tolerance for this species. Growth differences were minimal among plants receiving varied light exposure, although treatments ranged from 19% to 100% sunlight exposure. Light saturated photosynthesis of leaves on plants receiving 24% sunlight was achieved at a photosynthetic photon flux (PPF) of about one-fourth of that for the leaves on plants receiving 100% sunlight exposure. However, photosynthesis under conditions of extremely low PPF was higher for shade-grown plants than for full-sun plants. Shaded plants exhibited lower dark respiration, light compensation point, and light-saturated photosynthesis than full sun plants. Leaflet thickness, palisade layer number, and stomatal density of leaves of shaded plants were reduced compared with full sun plants. At seedling emergence and for several months thereafter, the plants responded to shade primarily with obligate sun plant characteristics. After the plants were established, however, responses to the varied light conditions indicated facultative structural and physiological characteristics.

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37

Gardner, Michael J., Katharine E. Hubbard, Carlos T. Hotta, Antony N. Dodd, and Alex A. R. Webb. "How plants tell the time." Biochemical Journal 397, no. 1 (June 14, 2006): 15–24. http://dx.doi.org/10.1042/bj20060484.

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Plants, like all eukaryotes and most prokaryotes, have evolved sophisticated mechanisms for anticipating predictable environmental changes that arise due to the rotation of the Earth on its axis. These mechanisms are collectively termed the circadian clock. Many aspects of plant physiology, metabolism and development are under circadian control and a large proportion of the transcriptome exhibits circadian regulation. In the present review, we describe the advances in determining the molecular nature of the circadian oscillator and propose an architecture of several interlocking negative-feedback loops. The adaptive advantages of circadian control, with particular reference to the regulation of metabolism, are also considered. We review the evidence for the presence of multiple circadian oscillator types located in within individual cells and in different tissues.

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38

Thondehaalmath, Tejas, Dilsher Singh Kulaar, Ramesh Bondada, and Ravi Maruthachalam. "Understanding and exploiting uniparental genome elimination in plants: insights from Arabidopsis thaliana." Journal of Experimental Botany 72, no. 13 (April 14, 2021): 4646–62. http://dx.doi.org/10.1093/jxb/erab161.

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Abstract Uniparental genome elimination (UGE) refers to the preferential exclusion of one set of the parental chromosome complement during embryogenesis following successful fertilization, giving rise to uniparental haploid progeny. This artificially induced phenomenon was documented as one of the consequences of distant (wide) hybridization in plants. Ten decades since its discovery, attempts to unravel the molecular mechanism behind this process remained elusive due to a lack of genetic tools and genomic resources in the species exhibiting UGE. Hence, its successful adoption in agronomic crops for in planta (in vivo) haploid production remains implausible. Recently, Arabidopsis thaliana has emerged as a model system to unravel the molecular basis of UGE. It is now possible to simulate the genetic consequences of distant crosses in an A. thaliana intraspecific cross by a simple modification of centromeres, via the manipulation of the centromere-specific histone H3 variant gene, CENH3. Thus, the experimental advantages conferred by A. thaliana have been used to elucidate and exploit the benefits of UGE in crop breeding. In this review, we discuss developments and prospects of CENH3 gene-mediated UGE and other in planta haploid induction strategies to illustrate its potential in expediting plant breeding and genetics in A. thaliana and other model plants.

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39

Chaki, Mounira, Juan C. Begara-Morales, and Juan B. Barroso. "Oxidative Stress in Plants." Antioxidants 9, no. 6 (June 3, 2020): 481. http://dx.doi.org/10.3390/antiox9060481.

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40

Yang, Xiusheng. "Plants and Microclimate: A Quantitative Approach to Environmental Plant Physiology." Agricultural and Forest Meteorology 66, no. 3-4 (November 1993): 267–68. http://dx.doi.org/10.1016/0168-1923(93)90075-s.

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41

Xoconostle, Beatriz, Francisco Arturo Ram, Leonardo Flores-Ele, and Roberto Ruiz-Medra. "Drought Tolerance in Crop Plants." American Journal of Plant Physiology 5, no. 5 (August 15, 2010): 241–56. http://dx.doi.org/10.3923/ajpp.2010.241.256.

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42

Andresen, Elisa, Edgar Peiter, and Hendrik Küpper. "Trace metal metabolism in plants." Journal of Experimental Botany 69, no. 5 (February 13, 2018): 909–54. http://dx.doi.org/10.1093/jxb/erx465.

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43

Cairns, A. J. "Fructan biosynthesis in transgenic plants." Journal of Experimental Botany 54, no. 382 (January 3, 2003): 549–67. http://dx.doi.org/10.1093/jxb/erg056.

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44

Hall, J. L. "Transition metal transporters in plants." Journal of Experimental Botany 54, no. 393 (October 29, 2003): 2601–13. http://dx.doi.org/10.1093/jxb/erg303.

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45

Hodge, A. "Plastic plants and patchy soils." Journal of Experimental Botany 57, no. 2 (September 19, 2005): 401–11. http://dx.doi.org/10.1093/jxb/eri280.

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46

Dueck, Tom, and Adrie van der Werf. "Are plants precursors for methane?" New Phytologist 178, no. 4 (June 2008): 693–95. http://dx.doi.org/10.1111/j.1469-8137.2008.02468.x.

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47

Harvey, Jagger JW, and Steven H. Strauss. "Towards physiological sculpture of plants." New Phytologist 181, no. 1 (December 3, 2008): 8–12. http://dx.doi.org/10.1111/j.1469-8137.2008.02697.x.

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48

Kiss, John Z. "Plants circling in outer space." New Phytologist 182, no. 3 (April 16, 2009): 555–57. http://dx.doi.org/10.1111/j.1469-8137.2009.02817.x.

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49

Poulsen, Michael, and Cameron R. Currie. "On ants, plants and fungi." New Phytologist 182, no. 4 (May 8, 2009): 785–88. http://dx.doi.org/10.1111/j.1469-8137.2009.02863.x.

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50

Long, P. E. "WATER, FUNGI AND PLANTS (Book)." Plant, Cell and Environment 10, no. 5 (July 1987): 437–38. http://dx.doi.org/10.1111/1365-3040.ep11603702.

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