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Journal articles on the topic 'Plant structure'

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1

Zhang, Shao Jun. "All Steel Structure Portal Frame Light Building Structure Design." Applied Mechanics and Materials 496-500 (January 2014): 2575–77. http://dx.doi.org/10.4028/www.scientific.net/amm.496-500.2575.

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According to the whole steel structure portal frame light plant design requirements, its architectural plane design, plant height determination, the determination of axis positioning, building facade design, from the column selection, auxiliary component orientation, profile design, daylighting, ventilated, plant, heat preservation, heat insulation design and other aspects are discussed.
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2

Spiker, S. "Plant Chromatin Structure." Annual Review of Plant Physiology 36, no. 1 (1985): 235–53. http://dx.doi.org/10.1146/annurev.pp.36.060185.001315.

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3

Nazarenko, M. M. "Induction of Winter Wheat Plant Structure Mutations by Chemomutagenesis." Agrology 3, no. 2 (2020): 57–65. http://dx.doi.org/10.32819/020008.

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4

Marshall, Andrew. "Plant PKS structure revealed." Nature Biotechnology 17, no. 8 (1999): 738. http://dx.doi.org/10.1038/11643.

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5

Ondřej, M. "Structure of Plant Genome." Biotechnology & Biotechnological Equipment 8, no. 1 (1994): 3–6. http://dx.doi.org/10.1080/13102818.1994.10818744.

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6

Vanderbilt, V. C. "Measuring plant canopy structure." Remote Sensing of Environment 18, no. 3 (1985): 281–94. http://dx.doi.org/10.1016/0034-4257(85)90063-x.

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7

Shi, Xian Jun, and Ji Hong Wu. "Analysis of Water Transport Properties for Plant Structured Textile Fabric." Advanced Materials Research 79-82 (August 2009): 87–90. http://dx.doi.org/10.4028/www.scientific.net/amr.79-82.87.

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Moisture/liquid transport in textile fabric is one of the critical factors affecting physiological comfort. Here we investigate the water transport properties of plant structures textile fabric, which was formed by mimicking the tree structure network. Our work shows that the water transport properties of the new type of material depend on its geometric structures, including the branching level and the diameter and length of the 0th branching level, and the structure fractal dimension. The more the length and the branching level, the lower the water transport capacity. A comparison of the plan
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8

Sraphet, Supajit, and Bagher Javadi. "Unraveling Techniques for Plant Microbiome Structure Analysis." Diversity 14, no. 3 (2022): 206. http://dx.doi.org/10.3390/d14030206.

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Microbiome plays vital role in the life. Study the microbiome of plants with great impact in the planet can provide significant information to solve many problems. Therefore, finding structural population of plant microbiome needs scientific approach. Revealing the specific biochemical and genetical approaches towards identification of specific population provided the growing bodies of methods and procedures to study and analysis the plant microbiomes. Thus, this mini-review paper presents the summarized of scientific methods for study, identify and structural population analysis of plant micr
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9

MUELLER, RICHARD J. "Ask the plant: investigating and teaching plant structure." Botanical Journal of the Linnean Society 150, no. 1 (2006): 73–78. http://dx.doi.org/10.1111/j.1095-8339.2006.00489.x.

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10

KIRCHOFF, BRUCE K., EVELIN PFEIFER, and ROLF RUTISHAUSER. "Plant structure ontology: How should we label plant structures with doubtful or mixed identities?" Zootaxa 1950, no. 1 (2008): 103–22. http://dx.doi.org/10.11646/zootaxa.1950.1.10.

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This paper discusses problems with labelling plant structures in the context of attempts to create a unified Plant Structure Ontology. Special attention is given to structures with mixed, or doubtful identities that are difficult or even impossible to label with a single term. In various vascular plants (and some groups of animals) the structural categories for the description of forms are less distinct than is often supposed. Thus, there are morphological misfits that do not fit exactly into one or the other category and to which it is difficult, or even impossible, to apply a categorical nam
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11

Kirchoff, Bruce K., Evelin Pfeifer, and Rolf Rutishauser. "Plant structure ontology: How should we label plant structures with doubtful or mixed identities? *." Zootaxa 1950, no. 1 (2008): 103–22. https://doi.org/10.11646/zootaxa.1950.1.10.

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Kirchoff, Bruce K., Pfeifer, Evelin, Rutishauser, Rolf (2008): Plant structure ontology: How should we label plant structures with doubtful or mixed identities? *. Zootaxa 1950 (1): 103-122, DOI: 10.11646/zootaxa.1950.1.10, URL: https://biotaxa.org/Zootaxa/article/view/zootaxa.1950.1.10
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12

Waite, S., M. J. A. Werger, P. J. M. van der Aert, H. J. During, and J. T. A. Verhoeven. "Plant Form and Vegetation Structure." Journal of Ecology 77, no. 4 (1989): 1174. http://dx.doi.org/10.2307/2260832.

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13

Michalska, K., G. Bujacz, and M. Jaskolski. "Crystal structure of plant asparaginase." Acta Crystallographica Section A Foundations of Crystallography 62, a1 (2006): s152. http://dx.doi.org/10.1107/s0108767306096966.

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14

Ishii, Tadashi, Jerry Thomas, Alan Darvill, and Peter Albersheim. "Structure of Plant Cell Walls." Plant Physiology 89, no. 2 (1989): 421–28. http://dx.doi.org/10.1104/pp.89.2.421.

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15

Eckardt, Nancy A. "Unexpected Structure of Plant Promoters." Plant Cell 26, no. 7 (2014): 2726. http://dx.doi.org/10.1105/tpc.114.129239.

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16

Siedow, J. N. "Plant Lipoxygenase: Structure and Function." Annual Review of Plant Physiology and Plant Molecular Biology 42, no. 1 (1991): 145–88. http://dx.doi.org/10.1146/annurev.pp.42.060191.001045.

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17

Passioura, JB. "Soil structure and plant growth." Soil Research 29, no. 6 (1991): 717. http://dx.doi.org/10.1071/sr9910717.

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Soil structure affects plant growth in many ways. Roots grow most rapidly in very friable soil, but their uptake of water and nutrients may be limited by inadequate contact with the solid and liquid phases of the soil. This contact is much more intimate in hard soil, but then the growth of the roots is strongly inhibited, so that their foraging ability is poor, and the plant may eventually become short of water or nutrients. However, many soils, even if hard, contain continuous macropores that provide niches for the roots to grow in. The presence of such macropores increases the extent of the
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18

Stevenson, Thomas T., Michael McNeil, Alan G. Darvill, and Peter Albersheim. "Structure of Plant Cell Walls." Plant Physiology 80, no. 4 (1986): 1012–19. http://dx.doi.org/10.1104/pp.80.4.1012.

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19

Thomas, Jerry R., Michael McNeil, Alan G. Darvill, and Peter Albersheim. "Structure of Plant Cell Walls." Plant Physiology 83, no. 3 (1987): 659–71. http://dx.doi.org/10.1104/pp.83.3.659.

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20

DAIE, JALEH. "Plant Membranes; Structure, Function, Biogensis." Soil Science 145, no. 6 (1988): 465. http://dx.doi.org/10.1097/00010694-198806000-00015.

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21

Richards, Eric J., and R. Kelly Dawe. "Plant centromeres: structure and control." Current Opinion in Plant Biology 1, no. 2 (1998): 130–35. http://dx.doi.org/10.1016/s1369-5266(98)80014-9.

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22

Michalska, Karolina, Grzegorz Bujacz, and Mariusz Jaskolski. "Crystal Structure of Plant Asparaginase." Journal of Molecular Biology 360, no. 1 (2006): 105–16. http://dx.doi.org/10.1016/j.jmb.2006.04.066.

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23

Sugden, A. M. "Plant community structure through time." Science 347, no. 6228 (2015): 1326. http://dx.doi.org/10.1126/science.347.6228.1326-b.

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24

Hackett, Wesley P. "Plant structure: Function and development." Scientia Horticulturae 57, no. 4 (1994): 359–60. http://dx.doi.org/10.1016/0304-4238(94)90119-8.

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25

Singh, Jyoti, M. Agrawal, and Deo Narayan. "Effect of power plant emissions on plant community structure." Ecotoxicology 3, no. 2 (1994): 110–22. http://dx.doi.org/10.1007/bf00143409.

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26

Chen, Zhe, Xu Dong Li, Shao Guang Shi, Hong Zhi Jiang, and Hui Jie Zhao. "Structured-Light Based Rapid 3D Measurement of Plant Canopy Structure." Applied Mechanics and Materials 701-702 (December 2014): 549–53. http://dx.doi.org/10.4028/www.scientific.net/amm.701-702.549.

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Density three dimensional plant canopy structure data has numerous applications in agriculture, but many existing 3D data collection approaches are time-consuming. In this paper, we present a measurement system based on structured-light for plant canopy structure data collection. The structured-light projector projects laser beam reflected by dual-oscillating mirror, arrives to the plant canopy, which is captured by a camera. We propose a new scanning mode, that is, during one exposure time of CCD camera, one mirror keeps moving in high frequency and small angle, while the other one maintains
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27

Xue, Zhicheng, Xiujun Cui, Qiang Pei, Jintu Zhong, Yongyi He, and Yao Zhang. "Seismic Isolation Performance of Nuclear Power Plant Containment Structures." Buildings 14, no. 6 (2024): 1650. http://dx.doi.org/10.3390/buildings14061650.

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Non-isolated structures have strong destructive effects and poor isolation effects when encountering earthquakes. Setting isolation bearings can prolong the natural vibration period of the structure, reduce the horizontal seismic response of the structure under the influence of variables such as acceleration, base reaction, and inter story displacement, and enhance the overall seismic performance of the structure. The new material—epoxy plate thick layer rubber isolation bearing—has unique advantages compared to other bearings, such as effective energy absorption, simple construction, and low
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28

Becerra, Judith X. "The impact of herbivore–plant coevolution on plant community structure." Proceedings of the National Academy of Sciences 104, no. 18 (2007): 7483–88. http://dx.doi.org/10.1073/pnas.0608253104.

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Coevolutionary theory proposes that the diversity of chemical structures found in plants is, in large part, the result of selection by herbivores. Because herbivores often feed on chemically similar plants, they should impose selective pressures on plants to diverge chemically or bias community assembly toward chemical divergence. Using a coevolved interaction between a group of chrysomelid beetles and their host plants, I tested whether coexisting plants of the Mexican tropical dry forest tend to be chemically more dissimilar than random. Results show that some of the communities are chemical
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29

Schaffer, W. M., and G. A. Fox. "Plant strategies and the dynamics and structure of plant communities." Bulletin of Mathematical Biology 51, no. 3 (1989): 409–11. http://dx.doi.org/10.1007/bf02460116.

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30

Austin, M. P. "Plant strategies and the dynamics and structure of plant communities." Trends in Ecology & Evolution 4, no. 1 (1989): 28–29. http://dx.doi.org/10.1016/0169-5347(89)90015-3.

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31

Facelli, José M., and Steward T. A. Pickett. "Plant litter: Its dynamics and effects on plant community structure." Botanical Review 57, no. 1 (1991): 1–32. http://dx.doi.org/10.1007/bf02858763.

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32

Burdon, J. J., and P. H. Thrall. "Resistance variation in natural plant populations." Plant Protection Science 38, SI 1 - 6th Conf EFPP 2002 (2002): S145—S150. http://dx.doi.org/10.17221/10342-pps.

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The general outcomes of long-term trajectories of coevolutionary interactions between specific hosts and pathogens are<br />set by the interaction of their life histories. However, within those outcomes the speed of co-evolutionary responses and<br />the extent of their expression in the resistance/virulence structure of wild plant and pathogen populations respectively,<br />are highly variable characters changing from place-to-place and time-to-time as a result of the interaction of host and<br />pathogen with the physical environment. As a consequence, understanding o
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33

Welinder, Karen G., J. Matthew Mauro, and Leif Nørskov-Lauritsen. "Structure of plant and fungal peroxidases." Biochemical Society Transactions 20, no. 2 (1992): 337–40. http://dx.doi.org/10.1042/bst0200337.

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34

Gasson, Peter, and Bryan G. Bowes. "A Colour Atlas of Plant Structure." Kew Bulletin 52, no. 3 (1997): 755. http://dx.doi.org/10.2307/4110311.

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35

Ben-Shem, Adam, Felix Frolow, and Nathan Nelson. "Crystal structure of plant photosystem I." Nature 426, no. 6967 (2003): 630–35. http://dx.doi.org/10.1038/nature02200.

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36

Möglich, Andreas, Xiaojing Yang, Rebecca A. Ayers, and Keith Moffat. "Structure and Function of Plant Photoreceptors." Annual Review of Plant Biology 61, no. 1 (2010): 21–47. http://dx.doi.org/10.1146/annurev-arplant-042809-112259.

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37

Li, Fu-Shuang, Pyae Phyo, Joseph Jacobowitz, Mei Hong, and Jing-Ke Weng. "The molecular structure of plant sporopollenin." Nature Plants 5, no. 1 (2018): 41–46. http://dx.doi.org/10.1038/s41477-018-0330-7.

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38

Blevins, Dale G., and Krystyna M. Lukaszewski. "BORON IN PLANT STRUCTURE AND FUNCTION." Annual Review of Plant Physiology and Plant Molecular Biology 49, no. 1 (1998): 481–500. http://dx.doi.org/10.1146/annurev.arplant.49.1.481.

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39

Unno, Hideaki, Tatsuya Uchida, Hajime Sugawara, et al. "Atomic Structure of Plant Glutamine Synthetase." Journal of Biological Chemistry 281, no. 39 (2006): 29287–96. http://dx.doi.org/10.1074/jbc.m601497200.

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40

Caspy, Ido, and Nathan Nelson. "Structure of the plant photosystem I." Biochemical Society Transactions 46, no. 2 (2018): 285–94. http://dx.doi.org/10.1042/bst20170299.

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Plant photosystem I (PSI) is one of the most intricate membrane complexes in nature. It comprises two complexes, a reaction center and light-harvesting complex (LHC), which together form the PSI–LHC supercomplex. The crystal structure of plant PSI was solved with two distinct crystal forms. The first, crystallized at pH 6.5, exhibited P21 symmetry; the second, crystallized at pH 8.5, exhibited P212121 symmetry. The surfaces involved in binding plastocyanin and ferredoxin are identical in both forms. The crystal structure at 2.6 Å resolution revealed 16 subunits, 45 transmembrane helices, and 2
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41

Barrier, Marianne, Elizabeth Friar, Robert Robichaux, and Michael Purugganan. "Interspecific evolution in plant microsatellite structure." Gene 241, no. 1 (2000): 101–5. http://dx.doi.org/10.1016/s0378-1119(99)00463-1.

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42

Orlov, Yu F. "Structure identification of a multidimensional plant." Differential Equations 42, no. 4 (2006): 607–11. http://dx.doi.org/10.1134/s0012266106040203.

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43

Kendall, Amy, Michele McDonald, Wen Bian, et al. "Structure of Flexible Filamentous Plant Viruses." Journal of Virology 82, no. 19 (2008): 9546–54. http://dx.doi.org/10.1128/jvi.00895-08.

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ABSTRACTFlexible filamentous viruses make up a large fraction of the known plant viruses, but in comparison with those of other viruses, very little is known about their structures. We have used fiber diffraction, cryo-electron microscopy, and scanning transmission electron microscopy to determine the symmetry of a potyvirus, soybean mosaic virus; to confirm the symmetry of a potexvirus, potato virus X; and to determine the low-resolution structures of both viruses. We conclude that these viruses and, by implication, most or all flexible filamentous plant viruses share a common coat protein fo
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44

Huang, Anthony H. C. "Structure of plant seed oil bodies." Current Opinion in Structural Biology 4, no. 4 (1994): 493–98. http://dx.doi.org/10.1016/s0959-440x(94)90210-0.

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45

Johansson, Kenth, Mustapha El-Ahmad, Rosmarie Friemann, Hans Jörnvall, Oskar Markovič, and Hans Eklund. "Crystal structure of plant pectin methylesterase." FEBS Letters 514, no. 2-3 (2002): 243–49. http://dx.doi.org/10.1016/s0014-5793(02)02372-4.

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46

Parkin, S. "Plant Lipid Biochemistry, Structure and Utilization." Biochemical Education 19, no. 2 (1991): 101. http://dx.doi.org/10.1016/0307-4412(91)90038-a.

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47

Friemann, R., K. Johansson, M. El-Ahmad, H. Jornvall, and O. Markovic. "Crystal structure of plant pectin methylesterase." Acta Crystallographica Section A Foundations of Crystallography 58, s1 (2002): c100. http://dx.doi.org/10.1107/s010876730208902x.

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48

Geiger, Dietmar. "Plant glucose transporter structure and function." Pflügers Archiv - European Journal of Physiology 472, no. 9 (2020): 1111–28. http://dx.doi.org/10.1007/s00424-020-02449-3.

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49

Albury, Mary S., Charles Affourtit, Paul G. Crichton, and Anthony L. Moore. "Structure of the Plant Alternative Oxidase." Journal of Biological Chemistry 277, no. 2 (2001): 1190–94. http://dx.doi.org/10.1074/jbc.m109853200.

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50

Lewinsohn, Thomas M., Paulo Inácio Prado, Pedro Jordano, Jordi Bascompte, and Jens M. Olesen. "Structure in plant-animal interaction assemblages." Oikos 113, no. 1 (2006): 174–84. http://dx.doi.org/10.1111/j.0030-1299.2006.14583.x.

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