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Journal articles on the topic 'Plant growth'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 May 2024

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1

Sakri, Faisal Abdulkadir, Noori Hassan Ghafor, and Hoshiar Abdula Aziz. "Effect of Some Plant Growth Regulators on Growth and Yield Component of Wheat – Plants CV. Bakrajo." Journal of Zankoy Sulaimani - Part A 5, no. 2 (April 25, 2002): 43–50. http://dx.doi.org/10.17656/jzs.10100.

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2

Carvalho, Deived Uilian de, Maria Aparecida da Cruz, Elisete Aparecida Fernandes Osipi, Conceição Aparecida Cossa, Ronan Carlos Colombo, and Maria Aparecida Fonseca Sorace. "PLANT GROWTH REGULATORS ON ATEMOYA SEEDS GERMINATION." Nucleus 15, no. 2 (October 30, 2018): 457–62. http://dx.doi.org/10.3738/1982.2278.2832.

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3

Uma Sankareswari, R. "Thermotolerant Bacillus as Plant Growth Promoting Rhizobacteria." International Journal of Science and Research (IJSR) 12, no. 5 (May 5, 2023): 2351–55. http://dx.doi.org/10.21275/sr23525092240.

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4

Végvári, György, and Edina Vidéki. "Plant hormones, plant growth regulators." Orvosi Hetilap 155, no. 26 (June 2014): 1011–18. http://dx.doi.org/10.1556/oh.2014.29939.

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Plants seem to be rather defenceless, they are unable to do motion, have no nervous system or immune system unlike animals. Besides this, plants do have hormones, though these substances are produced not in glands. In view of their complexity they lagged behind animals, however, plant organisms show large scale integration in their structure and function. In higher plants, such as in animals, the intercellular communication is fulfilled through chemical messengers. These specific compounds in plants are called phytohormones, or in a wide sense, bioregulators. Even a small quantity of these endogenous organic compounds are able to regulate the operation, growth and development of higher plants, and keep the connection between cells, tissues and synergy beween organs. Since they do not have nervous and immume systems, phytohormones play essential role in plants’ life. Orv. Hetil., 2014, 155(26), 1011–1018.

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5

Kandar, Mamat, Sony Suhandono, and I. Nyoman Pugeg Aryantha. "Growth Promotion of Rice Plant by Endophytic Fungi." Journal of Pure and Applied Microbiology 12, no. 3 (September 30, 2018): 1569–77. http://dx.doi.org/10.22207/jpam.12.3.62.

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6

Bortyanuy, I. O. "PLANT GROWTH-PROMOTING TRAITS OF ANTARCTIC ENDOPHYTIC BACTERIA." Biotechnologia Acta 15, no. 4 (August 31, 2022): 5–7. http://dx.doi.org/10.15407/biotech15.04.005.

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Successful colonization of Antarctic lands by vascular plants Deschampsia antarctica and Colobanthus quitensis and their adaptation to stressful environments is associated not only with climate change but also with the functioning of microbial groups of phylo- and endosphere of these plants. The aim of our study was to screen plant growth-promoting traits in endophytic bacteria of antarctic vascular plants. Materials and methods. We have studied 8 bacterial cultures isolated from D. antarctica collected during the 25th Ukrainian Antarctic Expedition (January-April 2020) along the Western part of the Antarctic Peninsula. Overnight liquid cultures were obtained on Nutrient Broth medium (HiMedia, Ltd.) in a shaking incubator (26 ℃, 160 rpm). Bacterial isolates were grown on Ashby's combined-nitrogen-free medium with sucrose. Drop collapse assay for cyclic lipopeptide production (CLP), motility assay, exoprotease production and phosphate solubilizing ability were performed using generally accepted methods. Results. All studied isolates have shown plant growth-promoting traits. The most abundant were nitrogen-fixing activity and motility. Both these play important role in plant colonization and promoting the growth of plants in harsh environments. The evidences of CLP were shown by two strains only. There was no notice of phosphate solubilizing ability and exoprotease production. Conclusions. Endophytic bacteria of antarctic vascular plants could support the growth and nutrition needs of the plants.

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7

NONAMI, Hiroshi. "Plant Growth Factory." TRENDS IN THE SCIENCES 15, no. 12 (2010): 80–82. http://dx.doi.org/10.5363/tits.15.12_80.

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8

Grubert, Marco. "SIMULATING PLANT GROWTH." XRDS: Crossroads, The ACM Magazine for Students 8, no. 2 (December 2001): 20. http://dx.doi.org/10.1145/567155.

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9

Grubert, Marco. "SIMULATING PLANT GROWTH." XRDS: Crossroads, The ACM Magazine for Students 8, no. 2 (December 2001): 20. http://dx.doi.org/10.1145/567155.1838744.

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10

Fankhauser, Christian, and John M. Christie. "Plant Phototropic Growth." Current Biology 25, no. 9 (May 2015): R384—R389. http://dx.doi.org/10.1016/j.cub.2015.03.020.

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11

Tonn, Nina, and Thomas Greb. "Radial plant growth." Current Biology 27, no. 17 (September 2017): R878—R882. http://dx.doi.org/10.1016/j.cub.2017.03.056.

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12

Grobelak, A., A. Napora, and M. Kacprzak. "Using plant growth-promoting rhizobacteria (PGPR) to improve plant growth." Ecological Engineering 84 (November 2015): 22–28. http://dx.doi.org/10.1016/j.ecoleng.2015.07.019.

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13

Bandopadhyay, Sandip. "Application of Plant Growth Promoting Bacillus thuringiensis as Biofertilizer on Abelmoschus esculentus Plants under Field Condition." Journal of Pure and Applied Microbiology 14, no. 2 (May 7, 2020): 1287–94. http://dx.doi.org/10.22207/jpam.14.2.24.

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14

Aras, Servet. "Shading Treatments Improved Plant Growth and Physiological Responses of Sweet Cherry Plants Subjected to Salt Stress." Alinteri Journal of Agricultural Sciences 36, no. 1 (February 6, 2021): 66–70. http://dx.doi.org/10.47059/alinteri/v36i1/ajas21011.

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15

Gunes, Adem, Kenan Karagoz, Metin Turan, Recep Kotan, Ertan Yildirim, Ramazan Cakmakci, and Fikrettin Sahin. "Fertilizer Efficiency of Some Plant Growth Promoting Rhizobacteria for Plant Growth." Research Journal of Soil Biology 7, no. 2 (February 1, 2015): 28–45. http://dx.doi.org/10.3923/rjsb.2015.28.45.

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16

Alikulov, B. S., V. V. Shuryhin, K. D. Davranov, and Z. F. Ismailov. "Halophytic Plant Halostachys belangeriana (Moq.) Botsch as a Source of Plant Growth-Promoting Endophytic Bacteria." Mikrobiolohichnyi Zhurnal 84, no. 4 (January 17, 2023): 30–39. http://dx.doi.org/10.15407/microbiolj84.04.030.

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Halostachys belangeriana (Moq.) Botsch also known as Halostachys caspica C. A. Mey belongs to the Chenopodiaceae family and is distributed in deserts of Asian countries. The plant grows in severe salinity and drought conditions and its survival and growth can be associated with the activity of endophytic bacteria. The objective of our research was to isolate and screen endophytic bacteria from Halostachys belangeriana for plant growth promotion and reveal their plant-beneficial traits. Methods. Halostachys belangeriana (Moq.) Botsch plants were collected from the saline soil of the Kyzylkum desert in Uzbekistan in spring. The endophytic bacteria were isolated from the tissues of plants by cutting the outer sterilized shoots and roots and putting them into the water to let bacteria come from the tissues into the water. The suspension was transferred onto Tryptic Soy Agar to let bacteria grow and form separate colonies. The colonies different in shape and color were used to get pure cultures of bacteria. The bacteria were screened using plant growth-promoting activity in Petri plates by inoculating wheat seeds with the suspension of isolated bacteria. The best plant growth promoters were identified by analyzing their 16S rRNA gene and comparing it with sequences registered in GenBank of NCBI. The strains were tested for wheat growth promotion in a pot experiment and then examined for their plant-benefi cial traits: N2-fixation, phosphates solubilization, production of indole-3-acetic acid (IAA), 1-aminocyclopropane-1-carboxylate deaminase (ACC-deaminase), and siderophores. Results. A total of 25 isolates of endophytic bacteria were obtained from the tissues of Halostachys belangeriana (Moq.) Botsch. Due to the high efficiency of isolates SSU-4, SSU-7, SSU-16, SSU-18, and SSU-21 in the stimulation of wheat shoot and root growth, they were chosen for identification and (OK559720), Bacillus endophyticus SSU-7 (OK559721), Bacillus subtilis SSU-16 (OK559722), Isoptericola halotolerans SSU-18 (OK559723) and Pseudomonas kilonensis SSU-21 (OK559724), respectively. The single inoculation of seeds with tested strains increased the root and shoot length and plant fresh weight. The coinoculation of seeds with a mixture of five strains resulted in an even more increase in plant growth parameters. It was revealed that the tested strains had at least two plant-beneficial properties. The strains B. pumilus SSU-4 and P. kilonensis SSU-21 had the ability for nitrogen fixation. All strains produced IAA; however, the most active IAA producer was P. kilonensis SSU-21. Three of five strains had phosphates solubilization ability and produced ACC-deaminase and siderophores. The strains B. pumilus SSU-4 and P. kilonensis SSU-21 possessed four of five tested plant-beneficial properties. The strains B. endophyticus SSU-7 and I. halotolerans SSU-18 had three of five tested plant-beneficial traits, and B. subtilis SSU-16 could just produce IAA and ACC-deaminase. Conclusions. This is the first report about the isolation of plant growth-promoting endophytic bacteria from the desert halophytic plant Halostachys belangeriana (Moq.) Botsch. The most efficient plant growth-promoting strains were: B. pumilus SSU-4, B. endophyticus SSU-7, B. subtilis SSU-16, I. halotolerans SSU-18, and P. kilonensis SSU-21. After field experiments, these strains can be suggested for use as bioinoculants improving plants growth.

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17

Gubiš, J., Z. Lajchová, L. Klčová, and Z. Jureková. "Influence of growth regulators on plant regeneration in tomato." Horticultural Science 32, No. 3 (November 23, 2011): 118–22. http://dx.doi.org/10.17221/3777-hortsci.

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We studied the effect of different plant growth regulators on in vitro regeneration and plant growth of three cultivars of tomato (Lycopersicon esculentum Mill.) from explants derived from hypocotyls and cotyledons of aseptically grown seedlings. The regeneration capacity was significantly influenced by cultivar and explant type. The highest number of shoots regenerated in both types of explants was recorded on MS medium supplemented with 1.0 mg/dm<sup>3</sup> zeatin and 0.1 mg/dm<sup>3</sup> IAA. The cultivar UC 82 showed the best regeneration capacity on all types of used media. The most responsive explants were hypocotyls with 90–92% regeneration in dependence on the used cultivars and mean production from 0.18 to 0.38 shoots per explant.  

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18

Mirziyatovich, Yakubov Mirdjamil, Akhmedov Shukhrat Mahmudovich, and Ruzimurodov Musurmon Dosmurod oglu. "CHARACTERISTICS OF SPRING GROWTH OF KIWI (ACTINIDIA DELICIOSA) PLANT." American Journal of Agriculture and Biomedical Engineering 04, no. 04 (April 1, 2022): 5–9. http://dx.doi.org/10.37547/tajabe/volume04issue04-02.

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In the article, kiwi (A.deliciosa) is a biologically resorbed fruit of the plant. The biochemical composition of the fruit contains the enzyme actinidine. This enzyme is needed to break down proteins and facilitate digestion. Kiwi fruit is one of the richest berries in terms of vitamin C content. Kiwi is a new type of fruit in Uzbekistan, and the exact area of plantations has not been statistically analyzed, but it is grown in the backyards of amateur gardeners who grow it. Scan grafting of the Hayward variety of kiwi plant was carried out in 3 periods. The second period was observed on March 15, when the retention rate of grafted buds was 82% or 13% higher than the period of the first grafting. The coefficient of variation in terms of welding times was low (V = 6.9%) and the coefficient of mean square deviation was X = 62.7 ± 3.1. The Hayward variety of kiwi plant has been created by means of grafting.

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19

J, Faheemah, and Dr John Dhanaseely A. "Smart Plant Growth on Hydroponics using Rain Water Harvesting." International Journal of Trend in Scientific Research and Development Volume-2, Issue-3 (April 30, 2018): 1928–31. http://dx.doi.org/10.31142/ijtsrd11488.

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20

Sarı, ömer. "Effects of plant biostimulants and plant growth regulator applications on plant growth in lilium 'Adelante'." Comunicata Scientiae 15 (October 31, 2023): e4191. http://dx.doi.org/10.14295/cs.v15.4191.

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This experiment was designed, it was determined the effects of mycorrhiza, vermicompost, promalin applications on development of plant properties in a bulbous plant, Lilyum 'Adelante. Flower branch length (cm), flower branch diameter (mm), internode number, flower bud number, flower bud length (cm), flower stem length (cm), flower width (cm), flower length (cm), number of leaves and leaf length (cm) were measured. The results showed that no treatment increased plant height more than control plants, but each application had different effects on other plant characteristics. As a matter of fact, mycorrhiza increased internode number, flower bud number, flower bud length, flower stem length, flower length, number of leaves and leaf length by 6.3%, 15.6%, 14.2%, 6%, 40%, 10.3%, 2.9% and 6%, respectively. Vermicompost increased flower bud length, flower length and leaf length by 6.6, 12, 15.3% and 16.1%, respectively. Promalin, on the other hand, increased the flower stem length, flower length and leaf length by 56.3% and 15.4%, respectively. The application of mycorrhiza together with Promalin did not have a different effect than the application of Promalin alone, and even showed a lower effect than the application of Promalin alone. Mycorrhiza, on the other hand, was the application that showed the best effect compared to other applications. Therefore, it can be recommended for plant growth in lilies. However, due to the effect of application time and dose on flowering time, it is possible to obtain different results in plant development in lilies.

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21

Preston, Gail M. "Plant perceptions of plant growth-promoting Pseudomonas." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 359, no. 1446 (June 29, 2004): 907–18. http://dx.doi.org/10.1098/rstb.2003.1384.

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Plant–associated Pseudomonas live as saprophytes and parasites on plant surfaces and inside plant tissues. Many plant–associated Pseudomonas promote plant growth by suppressing pathogenic micro–organisms, synthesizing growth–stimulating plant hormones and promoting increased plant disease resistance. Others inhibit plant growth and cause disease symptoms ranging from rot and necrosis through to developmental dystrophies such as galls. It is not easy to draw a clear distinction between pathogenic and plant growth–promoting Pseudomonas . They colonize the same ecological niches and possess similar mechanisms for plant colonization. Pathogenic, saprophytic and plant growth–promoting strains are often found within the same species, and the incidence and severity of Pseudomonas diseases are affected by environmental factors and host–specific interactions. Plants are faced with the challenge of how to recognize and exclude pathogens that pose a genuine threat, while tolerating more benign organisms. This review examines Pseudomonas from a plant perspective, focusing in particular on the question of how plants perceive and are affected by saprophytic and plant growth–promoting Pseudomonas (PGPP), in contrast to their interactions with plant pathogenic Pseudomonas . A better understanding of the molecular basis of plant–PGPP interactions and of the key differences between pathogens and PGPP will enable researchers to make more informed decisions in designing integrated disease–control strategies and in selecting, modifying and using PGPP for plant growth promotion, bioremediation and biocontrol.

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22

van Loon, L. C. "Plant responses to plant growth-promoting rhizobacteria." European Journal of Plant Pathology 119, no. 3 (June 5, 2007): 243–54. http://dx.doi.org/10.1007/s10658-007-9165-1.

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23

Schröder, F. "TECHNOLOGICAL DEVELOPMENT, PLANT GROWTH AND ROOT ENVIRONMENT OF THE PLANT PLANE HYDROPONIC SYSTEM." Acta Horticulturae, no. 361 (June 1994): 201–9. http://dx.doi.org/10.17660/actahortic.1994.361.18.

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24

Ghori, Tameezuddin Khan, Anusuya D. Anusuya. D, and Geetha M. Geetha.M. "Growth of Nursery Grown Micro Propagated Bamboo (Bambusa Tulda .L) Inoculated with Arbuscular Mycorrhizal Fungus and Plant Growth Promoting Rhizobacteria (Pgpr)." International Journal of Scientific Research 3, no. 6 (June 1, 2012): 53–54. http://dx.doi.org/10.15373/22778179/june2014/21.

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25

Rudolph, N., N. Labuschagne, and T. A. S. Aveling. "The effect of plant growth promoting rhizobacteria on seed germination and seedling growth of maize." Seed Science and Technology 43, no. 3 (December 15, 2015): 507–18. http://dx.doi.org/10.15258/sst.2015.43.3.04.

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26

Ohara, Akio. "Light and Plant-growth." JOURNAL OF THE ILLUMINATING ENGINEERING INSTITUTE OF JAPAN 77, no. 1 (1993): 40–42. http://dx.doi.org/10.2150/jieij1980.77.1_40.

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27

Fox, Theodore C. "Handbook of Plant Growth." Crop Science 43, no. 4 (July 2003): 1575–76. http://dx.doi.org/10.2135/cropsci2003.1575.

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28

Schopfer, P. "Biomechanics of plant growth." American Journal of Botany 93, no. 10 (October 1, 2006): 1415–25. http://dx.doi.org/10.3732/ajb.93.10.1415.

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29

Hines, Pamela J. "Plant cell growth regulation." Science 373, no. 6554 (July 29, 2021): 529.2–529. http://dx.doi.org/10.1126/science.373.6554.529-b.

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30

Crawford, R. M. M., and T. T. Kozlowski. "Flooding and Plant Growth." Journal of Ecology 73, no. 3 (November 1985): 1069. http://dx.doi.org/10.2307/2260173.

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31

Lugtenberg, Ben, and Faina Kamilova. "Plant-Growth-Promoting Rhizobacteria." Annual Review of Microbiology 63, no. 1 (October 2009): 541–56. http://dx.doi.org/10.1146/annurev.micro.62.081307.162918.

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32

MATSUBAYASHl, Yoshikatsu, and Youji SAKAGAMI. "Plant Cell Growth Factor." Nippon Nōgeikagaku Kaishi 70, no. 5 (1996): 588–90. http://dx.doi.org/10.1271/nogeikagaku1924.70.588.

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33

Shimizu, Hiroshi. "Light for Plant Growth." JOURNAL OF THE ILLUMINATING ENGINEERING INSTITUTE OF JAPAN 87, no. 4 (2003): 268–70. http://dx.doi.org/10.2150/jieij1980.87.4_268.

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34

Gregorczyk, A. "Richards Plant Growth Model." Journal of Agronomy and Crop Science 181, no. 4 (November 1998): 243–47. http://dx.doi.org/10.1111/j.1439-037x.1998.tb00424.x.

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35

Mandava, N. B. "Plant Growth-Promoting Brassinosteroids." Annual Review of Plant Physiology and Plant Molecular Biology 39, no. 1 (June 1988): 23–52. http://dx.doi.org/10.1146/annurev.pp.39.060188.000323.

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36

Miransari, Mohammad. "Plant Growth Promoting Rhizobacteria." Journal of Plant Nutrition 37, no. 14 (August 30, 2014): 2227–35. http://dx.doi.org/10.1080/01904167.2014.920384.

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37

Vanhaeren, Hannes, Dirk Inzé, and Nathalie Gonzalez. "Plant Growth Beyond Limits." Trends in Plant Science 21, no. 2 (February 2016): 102–9. http://dx.doi.org/10.1016/j.tplants.2015.11.012.

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38

Napier, Richard. "Growth of plant culture." Trends in Plant Science 8, no. 12 (December 2003): 568–69. http://dx.doi.org/10.1016/j.tplants.2003.10.005.

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39

GREENLAND, D. J. "Flooding and Plant Growth." Soil Science 141, no. 3 (March 1986): 244. http://dx.doi.org/10.1097/00010694-198603000-00011.

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40

Singh, Jay Shankar. "Plant Growth Promoting Rhizobacteria." Resonance 18, no. 3 (March 2013): 275–81. http://dx.doi.org/10.1007/s12045-013-0038-y.

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41

Jacquard, P. "Flooding and plant growth." Agriculture, Ecosystems & Environment 18, no. 1 (October 1986): 89–90. http://dx.doi.org/10.1016/0167-8809(86)90181-7.

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42

Hills, P. N., L. M. Kotze, L. E. Steenkamp, N. N. Ludidi, and J. M. Kossmann. "Plant growth promoting substances." South African Journal of Botany 75, no. 2 (April 2009): 405. http://dx.doi.org/10.1016/j.sajb.2009.02.061.

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43

VISSER, E. J. W. "Flooding and Plant Growth." Annals of Botany 91, no. 2 (January 1, 2003): 107–9. http://dx.doi.org/10.1093/aob/mcg014.

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44

Boyer, John S., and Wendy K. Silk. "Hydraulics of plant growth." Functional Plant Biology 31, no. 8 (2004): 761. http://dx.doi.org/10.1071/fp04062.

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Multicellular plants rely on growth in localised regions that contain small, undifferentiated cells and may be many millimetres from the nearest differentiated xylem and phloem. Water and solutes must move to these small cells for their growth. Increasing evidence indicates that after exiting the xylem and phloem, water and solutes are driven to the growing cells by gradients in water potential and solute potential or concentration. The gradients are much steeper than in the vascular transport system and can change in magnitude or suffer local disruption with immediate consequences for growth. Their dynamics often obscure how turgor drives wall extension for growth, and different flow paths for roots and shoots have different dynamics. In this review, the origins of the gradients, their mode of action and their consequences are discussed, with emphasis on how their dynamics affect growth processes.

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45

Abbott, Alison. "Plant biology: Growth industry." Nature 468, no. 7326 (December 2010): 886–88. http://dx.doi.org/10.1038/468886a.

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46

Firn, Richard. "Plant Growth Substances 1988." Phytochemistry 31, no. 3 (March 1992): 1091. http://dx.doi.org/10.1016/0031-9422(92)80091-r.

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47

Logvenkov, S. A. "Modeling plant root growth." Fluid Dynamics 28, no. 1 (1993): 69–75. http://dx.doi.org/10.1007/bf01055667.

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48

Herms, Daniel A., and William J. Mattson. "Plant growth and defense." Trends in Ecology & Evolution 9, no. 12 (December 1994): 488. http://dx.doi.org/10.1016/0169-5347(94)90319-0.

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49

Bianco, Carmen. "Plant-Growth-Promoting Bacteria." Plants 13, no. 10 (May 11, 2024): 1323. http://dx.doi.org/10.3390/plants13101323.

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50

AlAli, Heba Adel, Ashraf Khalifa, and Mohammed Almalki. "Plant Growth-Promoting Bacterium from Non-Agricultural Soil Improves Okra Plant Growth." Agriculture 12, no. 6 (June 16, 2022): 873. http://dx.doi.org/10.3390/agriculture12060873.

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Beneficial soil microorganisms influence nutrient recycling, soil fertility, plant growth, and productivity and reduce chemical fertilizer application. This study aimed to isolate bacteria from non-agricultural soils in the Al-Ahsa region and characterize the bacteria with the best biostimulating characteristics at the physiological, biochemical, and molecular level. DPM17, a bacterial isolate, promotes plant growth through phosphate solubilization, nitrogen fixation, and ammonia production. DPM17 also produces the phytohormones, indole acetic acid (IAA; 4.516 μg mL−1) and gibberellin (1.33 µg mL−1), and ammonia (0.06 µg mL−1). Additionally, DPM17 grows in the presence of up to 10% NaCl, indicating its halophilic nature. DPM17 was identified as Bacillus baekryungensis based on comparative sequence analysis of the 16S rRNA gene, and neighbor-joining phylogenetic analyses indicated that DPM17 was 96.51% identified to Bacillus sp. DPM17 inoculation substantially improved Abelmoschus esculentus (okra) root length, lateral root count, and dry weight from 7.03 to 9.41 (p = 0.03), 3.2 to 7.2, and 6 to 13 mg (p = 0.032), respectively. The results suggest that DPM17 enhances plant growth and can be exploited to develop efficient formulations for sustainable agriculture and food security in Saudi Arabia.

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