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Journal articles on the topic 'Anatomy of leaf'

Author: Grafiati

Published: 4 June 2025

Last updated: 15 July 2025

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1

Y Ingle, Sneha, and Surekha S Tayade. "Anatomy Concerning Leaf of Ficus Carica Linn." International Journal of Science and Research (IJSR) 10, no. 4 (2021): 1054–56. https://doi.org/10.21275/sr21421211222.

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2

VIEIRA, R. C., D. M. S. GOMES, L. S. SARAHYBA, and R. C. O. ARRUDA. "Leaf anatomy of three herbaceous bamboo species." Brazilian Journal of Biology 62, no. 4b (2002): 907–22. http://dx.doi.org/10.1590/s1519-69842002000500021.

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Fully developed leaves of Cryptochloa capillata (Swallen) Soderstrom, Raddia brasilienses Bertol and Pharus lappulaceus Aublet (Poaceae: Bambusoideae) were collected at Restinga de Jacarepiá, Environment Proctection Area of Massambaba, county of Rio de Janeiro, State of Rio de Janeiro, Brazil, and studied by optical microscope. Leaf anatomy is described in order to contribute to the Poaceae family study. Anatomic features observed in the three studied species such as: midrib with complex vascular system, mesophyll consisting of tabular lobed chlorophyllous elements and fusoid cells, vascular b

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3

Rudall, Paula. "Leaf anatomy inTigridieae (Iridaceae)." Plant Systematics and Evolution 175, no. 1-2 (1991): 1–10. http://dx.doi.org/10.1007/bf00942141.

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4

Rôças, Giselle, Cláudia Franca Barros, and Fábio Rubio Scarano. "Leaf anatomy plasticity of." Trees 11, no. 8 (1997): 469. http://dx.doi.org/10.1007/s004680050109.

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5

Chantarasuwan, Bhanumas, Pieter Baas, Bertie-Joan van Heuven, Claudia Baider, and Peter C. van Welzen. "Leaf anatomy ofFicussubsectionUrostigma(Moraceae)." Botanical Journal of the Linnean Society 175, no. 2 (2014): 259–81. http://dx.doi.org/10.1111/boj.12165.

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6

Pinedo, André Silva, Renata Corrêa Martins, Regina Célia de Oliveira, and Sueli Maria Gomes. "Leaf anatomy inAllagoptera(Arecaceae)." Botanical Journal of the Linnean Society 182, no. 2 (2016): 361–75. http://dx.doi.org/10.1111/boj.12439.

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7

Palhares, D., C. Silveira, L. Zaidan, and L. Pereira. "Leaf anatomy ofSmilax goyazana(Smilacaceae)." Acta Botanica Hungarica 51, no. 1-2 (2009): 115–27. http://dx.doi.org/10.1556/abot.51.2009.1-2.14.

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8

Zona, Scott. "Leaf Anatomy of the Goetzeaceae." Aliso 12, no. 2 (1989): 303–12. http://dx.doi.org/10.5642/aliso.19891202.07.

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9

Rudall, Paula, and Brian Mathew. "Leaf Anatomy in Crocus (Iridaceae)." Kew Bulletin 45, no. 3 (1990): 535. http://dx.doi.org/10.2307/4110516.

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10

ARROYO, SILVIA. "Leaf anatomy in the Tecophilaeaceae." Botanical Journal of the Linnean Society 93, no. 4 (1986): 323–28. http://dx.doi.org/10.1111/j.1095-8339.1986.tb01029.x.

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11

BREITWIESER, I. "Leaf anatomy ofRaouliaHook.f. (Compositae, Gnaphalieae)." Botanical Journal of the Linnean Society 126, no. 3 (1998): 217–35. http://dx.doi.org/10.1006/bojl.1997.0139.

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12

Koller, Alan L., and Thomas L. Rost. "LEAF ANATOMY IN SANSEVIERIA (AGAVACEAE)." American Journal of Botany 75, no. 5 (1988): 615–33. http://dx.doi.org/10.1002/j.1537-2197.1988.tb13485.x.

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13

Sarala, C. Tadavi, and V. Bhadane Vijay. "TAXONOMIC SIGNIFICANCE OF THE RACHIS, PETIOLE AND PETIOLULE ANATOMY IN SOME EUPHORBIACEAE." Biolife 2, no. 3 (2022): 850–57. https://doi.org/10.5281/zenodo.7220482.

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<strong>ABSTRACT</strong> Anatomy of rachis, petiole and petiolule in 43 species and 20 genera of Euphorbiaceae are investigated. The mechanical tissues in these organs are invariably sclerenchymatous and collenchymatous. The xylem elements are additionally mechanical in function. The occurrence of vascular tissues is in the form of distinct bundles, only an arc-shaped strand or a continuous cylinder. The cortical bundles are noted in <em>Aporosa </em>and <em>Jatropha gossypiifolia</em> while unequal sized central vascular bundles are observed in <em>Mallotus nudiflorus </em>and <em>M. philipp

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14

Renninger, Heidi, Tyler Durbin, Austin Gentry, and Zeima Kassahun. "Relationships between Leaf Anatomy and Physiological Functioning of Southern US Oak Species Differing in Flood Tolerance." Forests 11, no. 1 (2020): 73. http://dx.doi.org/10.3390/f11010073.

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Research Highlights: Bottomland oaks receive less attention than upland species, however their adaptations to flooding and summer water stress will extend our understanding of the oak genus and links between physiology and leaf anatomy. Background and objectives: Determining links between leaf anatomy and physiology can aid in parameterizing dynamic global vegetation models for oak systems, therefore we sought to (1) compare leaf anatomic, nutrient, and physiological parameters for bottomland oaks differing in flood tolerance, (2) determine correlations across parameters and determine which an

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15

Martins, Maria Bernadete Gonçalves, and Rodrigo Zieri. "Leaf anatomy of rubber-tree clones." Scientia Agricola 60, no. 4 (2003): 709–13. http://dx.doi.org/10.1590/s0103-90162003000400015.

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Rubber trees are easily recognizable for being woody, medium to large-sized plants, having a typical deciduous behavior, and especially because they produce latex. The purpose of this work was to study the anatomy and morphology of the leaf, comparing rubber tree &91;Hevea brasiliensis (Willd. ex Adr. de Juss.) Muell.-Arg.&93; clones (RRIM 600 and GT 1) grafted on the same root stock (Tjir 1), grown under the same climatic and soil conditions. This study allowed clones to be differentiated and also provided information on the location and disposition of laticifers in the leaf tissue. C

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16

Pridgeon, Alec M. "Systematic Leaf Anatomy of Caladenia (Orchidaceae)." Kew Bulletin 48, no. 3 (1993): 533. http://dx.doi.org/10.2307/4118720.

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17

AL-Saghir, Mohannad G., Duncan M. Porter, and Erik T. Nilsen. "Leaf Anatomy of Pistacia Species (Anacardiaceae)." Journal of Biological Sciences 6, no. 2 (2006): 242–44. http://dx.doi.org/10.3923/jbs.2006.242.244.

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18

ERXU, PI, PENG QIUFA, LU HONGFEI, et al. "Leaf morphology and anatomy ofCamelliasectionCamellia(Theaceae)." Botanical Journal of the Linnean Society 159, no. 3 (2009): 456–76. http://dx.doi.org/10.1111/j.1095-8339.2009.00952.x.

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19

PRIDGEON, ALEC M. "Systematic leaf anatomy of Caladeniinae (Orchidaceae)." Botanical Journal of the Linnean Society 114, no. 1 (1994): 31–48. http://dx.doi.org/10.1111/j.1095-8339.1994.tb01922.x.

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20

Burrows, GE. "Leaf Axil Anatomy of the Araucariaceae." Australian Journal of Botany 35, no. 6 (1987): 631. http://dx.doi.org/10.1071/bt9870631.

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Well defined, persistent meristems, which possess neither a bud-like organisation nor vascular connections with the central vascular cylinder, were found in the apparently blank leaf axils of six species of Agathis and 13 species of Araucaria. In other conifers, leaf axils of similar external appearance are usually reported to lack, or gradually lose, any specialised bud-forming tissues. Meristems were found in all axils investigated and in this respect the Araucariaceae approach the typical angiospermous condition of a bud in each leaf axil. Evidence is presented that the type of axillary mer

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21

Terashima, Ichiro. "Anatomy of non-uniform leaf photosynthesis." Photosynthesis Research 31, no. 3 (1992): 195–212. http://dx.doi.org/10.1007/bf00035537.

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22

Klimenko, E. "Anatomy of floating and submerged leaves of heterophyllous plant of Nymphaea candida L." Modern Phytomorphology 6 (April 1, 2014): 327–30. https://doi.org/10.5281/zenodo.160793.

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The data on anatomy of floating and submerged leaves of heterophyllous aquatic plant Nymphaea candida L. are presented. Anatomy of floating leaves is shown to be different from that of submerged leaves: the absence of stomata, asterosclereids, and differentiated parenchyma, as well as by reduce intercellular volume and leaf width. Common patterns of leaf structure plasticity of aquatic heterophyllous plants in dependence on the environment are discussed.

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23

Pangemanan, Euis F. S., Semuel P. Ratag, and Marthen T. Lasut. "Comparative Anatomy Of Leaves Of Several Types Of Ficus." Jurnal Agroekoteknologi Terapan 3, no. 2 (2022): 382–87. http://dx.doi.org/10.35791/jat.v3i2.44519.

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Leaf anatomy studies need to be carried out to support morphological plant identification. Leaf anatomy was observed because leaves have varying tissue structures. The characteristics of stomatal density, epidermal cell shape, and leaf mesophyll structure are constant in each species so that they can be used as a reference. The aim of the study was to identify the anatomical characters of the leaves of various types of Ficus. Samples were collected from Tahura Gunung Tumpa. Observation of the anatomical structure of Ficus leaves using a light microscope based on Sass (1951) and Johansen (1940)

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24

Wooge, Jon D., and John A. Barden. "Seasonal Changes in Specific Leaf Weight and Leaf Anatomy of Apple." HortScience 22, no. 2 (1987): 292–94. http://dx.doi.org/10.21273/hortsci.22.2.292.

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Abstract Newly expanded interior canopy leaves of apple (Malus domestica Borkh.) had lower specific leaf weight (SLW), leaf thickness, palisade depth, and number of palisade cell layers than middle or peripheral leaves from late May to early October. Leaves on the periphery of the canopy had the highest SLW values at all sample dates. Differences in leaf SLW, leaf thickness, and palisade depth between interior and peripheral leaves increased as the season progressed, primarily due to increases in peripheral leaves that developed later in the season. Regression analysis showed SLW to be signifi

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25

Daningsih, E., A. N. Mardiyyanigsih, Y. O. Da Costa, R. Primawati, and S. Karlina. "Changes of stomatal distribution and leaf thickness in response to transpiration rate in six dicot plant species." IOP Conference Series: Earth and Environmental Science 976, no. 1 (2022): 012060. http://dx.doi.org/10.1088/1755-1315/976/1/012060.

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Abstract Changes in leaf anatomy can be influenced by the surrounding environment and several other factors. Shade plants or ornamental plants themselves also have their characteristics in responding to surrounding conditions through transpiration. This study aimed to measure the rate of transpiration related to changes in the distribution of stomata and leaf thickness of six types of dicot ornamental plants and to describe the leaf anatomy of each type. The experiment used Completely Randomized Design (CRD) with six types of plants as treatment with three replications. Transpiration rate was

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26

Hill, Kathryn E., Stuart C. Brown, Alice Jones, Damien Fordham, and Robert S. Hill. "Modelling Climate Using Leaves of Nothofagus cunninghamii—Overcoming Confounding Factors." Sustainability 15, no. 9 (2023): 7603. http://dx.doi.org/10.3390/su15097603.

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Fossil leaf anatomy has previously been used as a proxy for paleoclimate. However, the exposure of leaves to sun or shade during their growth can lead to morphotype differences that confound the interpretation of fossil leaf anatomy in relation to climate and prevent reliable paleoclimate reconstruction. This work aims to model the differences in leaf anatomy that are due to various climatic drivers and differences attributable to sun or shade positions, using Nothofagus cunninghamii as the model species. Leaves from the sun and shade parts of three trees have been sampled from each of 11 site

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27

Xiong, Dongliang, and Jaume Flexas. "Leaf anatomical characteristics are less important than leaf biochemical properties in determining photosynthesis responses to nitrogen top-dressing." Journal of Experimental Botany 72, no. 15 (2021): 5709–20. http://dx.doi.org/10.1093/jxb/erab230.

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Abstract The photosynthetic capacity of leaves is dramatically influenced by nitrogen (N) availability in the soil, as CO2 concentration in chloroplasts and photosynthetic biochemical capacity are related to leaf N content. The relationship between mesophyll conductance (gm) and leaf N content was expected to be shaped by leaf anatomical traits. However, the increased gm in mature leaves achieved by N top-dressing is unlikely to be caused by changes in leaf anatomy. Here, we assessed the impacts of N supply on leaf anatomical, biochemical, and photosynthetic features, specifically, the dynamic

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28

Seshavatharam, V., and M. Srivalli. "Systematic leaf anatomy of some Indian mangroves." Proceedings / Indian Academy of Sciences 99, no. 6 (1989): 557–65. http://dx.doi.org/10.1007/bf03053425.

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29

Rudall, Paula. "Leaf Anatomy and Systematics of Mariceae (Iridaceae)." Kew Bulletin 48, no. 1 (1993): 151. http://dx.doi.org/10.2307/4115760.

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30

Dickison, William. "Stem and Leaf Anatomy of the Alseuosmiaceae." Aliso 12, no. 3 (1989): 567–78. http://dx.doi.org/10.5642/aliso.19891203.11.

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31

BREITWIESER, ILSE, and JOSEPHINE M. WARD. "Leaf anatomy of Raoulia Hook.f. (Compositae, Gnaphalieae)." Botanical Journal of the Linnean Society 126, no. 3 (1998): 217–35. http://dx.doi.org/10.1111/j.1095-8339.1998.tb02528.x.

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32

HOFREITER, ANTON, and OLE B. LYSHEDE. "Functional leaf anatomy of Bomarea Mirb. (Alstroemeriaceae)." Botanical Journal of the Linnean Society 152, no. 1 (2006): 73–90. http://dx.doi.org/10.1111/j.1095-8339.2006.00540.x.

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33

SUGDEN, ANDREW M. "Leaf anatomy in a Venezuelan montane forest." Botanical Journal of the Linnean Society 90, no. 4 (1985): 231–41. http://dx.doi.org/10.1111/j.1095-8339.1985.tb00383.x.

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34

RUDALL, PAULA, and PETER GOLDBLATT. "Leaf anatomy and phylogeny of Ixioideae (Iridaceae)." Botanical Journal of the Linnean Society 106, no. 4 (1991): 329–45. http://dx.doi.org/10.1111/j.1095-8339.1991.tb02297.x.

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35

WILKINSON, HAZEL P. "Leaf anatomy of the Pittosporaceae R. Br." Botanical Journal of the Linnean Society 110, no. 1 (1992): 1–59. http://dx.doi.org/10.1111/j.1095-8339.1992.tb00415.x.

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36

RUDALL, PAULA, and PETER GOLDBLATT. "Leaf anatomy and systematics of Homeriinae (Iridaceae)." Botanical Journal of the Linnean Society 111, no. 3 (1993): 379–97. http://dx.doi.org/10.1111/j.1095-8339.1993.tb01911.x.

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37

Wilkinson, Hazel P. "Leaf anatomy of ‘Bigaignon Sauvage’ from Mauritius." Pharmaceutical Biology 37, no. 4 (1999): 307–13. http://dx.doi.org/10.1076/phbi.37.4.307.5799.

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38

Terashima, Ichiro, Yuko T. Hanba, Danny Tholen, and Ülo Niinemets. "Leaf Functional Anatomy in Relation to Photosynthesis." Plant Physiology 155, no. 1 (2010): 108–16. http://dx.doi.org/10.1104/pp.110.165472.

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39

Barroso, Arthur Arrobas Martins, Esteban Galeano, Alfredo Junior Paiola Albrecht, Fabrícia Cristina Dos Reis, and Ricardo Victoria Filho. "Does Sourgrass leaf anatomy influence glyphosate resistance?" Comunicata Scientiae 6, no. 4 (2015): 445. http://dx.doi.org/10.14295/cs.v6i4.1124.

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Sourgrass(Digitaria insularis, L. Mez ex Ekman)is a weed that requires high rates of glyphosate ((N-[phosphonomethyl]-glycine) forcontrol, verylittle of the herbicide applied isabsorbed by theleaves. Morphological and histological differences in leaves of glyphosate-resistant and glyphosate-susceptible plantsshould explain the contrast of variance between herbicide susceptibility. Leaves of different growth andphenological stages were collected and submitted to histological andelectron microscopy scanning analysis. Those plants were also submitted to a glyphosate dose-response curve analysis.

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40

Santos, FC, AS Freitas, EM de Castro, LC Davide, F. Souza Sobrinho, and VH Techio. "Leaf anatomy and nutritive values ofBrachiaria ruziziensisgenotypes." New Zealand Journal of Agricultural Research 57, no. 2 (2014): 128–35. http://dx.doi.org/10.1080/00288233.2014.897237.

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41

Demétrio, Angela M., Makeli G. Lusa, Duane F. Lima, and Ana Claudia Rodrigues. "Leaf anatomy of Varronia polycephala Lam. (Cordiaceae)." Flora 271 (October 2020): 151677. http://dx.doi.org/10.1016/j.flora.2020.151677.

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42

Henderson, Flor. "Leaf anatomy of the genus Leopoldinia (Arecaceae)." Journal of the Torrey Botanical Society 140, no. 3 (2013): 369–72. http://dx.doi.org/10.3159/torrey-d-12-00027.1.

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43

Feng, Zhuo, Yong Lv, Yun Guo, Hai-Bo Wei, and Hans Kerp. "Leaf anatomy of a late Palaeozoic cycad." Biology Letters 13, no. 11 (2017): 20170456. http://dx.doi.org/10.1098/rsbl.2017.0456.

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Today, cycads are a small group of gymnospermous plants with a limited distribution in the (sub)tropics, but they were major constituents of Mesozoic floras. Fossil leaves sporadically found in latest Carboniferous and Permian floras have putatively been ascribed to cycads. However, their true affinity remains unclear due to the lack of anatomical evidence. Virtually all modern cycads have pinnate leaves, but this type of leaf morphology is by no means unique for cycads. Pinnate leaves of Plagiozamites oblongifolius Halle 1927 with well-preserved cuticles showing the epidermal anatomy are here

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44

Nuzhyna, N., L. Rybak, E. Konovalova, and V. Menshova. "Leaf anatomy of Geranium sanguineum L. (Geraniaceae)." Modern Phytomorphology 6 (April 1, 2014): 315–18. https://doi.org/10.5281/zenodo.160788.

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The results of anatomical investigation of lamina and petiole of Geranium sanguineum L. are presented. Here were established anatomical features that characterize G. sanguineum as mesoxerophytic plant.

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45

Codreanu, V. "Quantitative anatomy of grapevine (Vitis L.) leaf blade." Modern Phytomorphology 4 (April 1, 2013): 199–207. https://doi.org/10.5281/zenodo.161371.

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Current investigations were conducted to clarify the features of grapevine which are adaptive to drought and can be used in selection and introduction of Vitis L. There are determined biometric values of 21 morpho-anatomic characters of leaf blade for 10 species of grapevine, 10 cultivars of V. vinifera L. and 10 distant hybrids V. vinifera × Muscadinia rotundifolia Michx. As a result of this study 6 leaf blade quantitative characters which determine relative grapevine drought resistance were described. The most drought resistant species, sorts and hybrids of grapevine are that which have: a)

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46

Ellis, R. P. "Leaf anatomy of the South African Danthonieae (Poaceae). XVI. The genus Urochlaena." Bothalia 18, no. 1 (1988): 101–4. http://dx.doi.org/10.4102/abc.v18i1.990.

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The leaf blade anatomy of Urochlaena pusilla Nees is described and illustrated. The transectional anatomy is non- Kranz with diffuse but uniformly distributed chlorenchyma. The abaxial epidermis has dome-shaped stomata, dumbbellshaped silica bodies, elongated finger-like microhairs, and cushion-based macrohairs may or may not be present. This type of arundinoid anatomy closely resembles that o f Tribolium Desv., Chaetobromus Nees, Schismus Beauv., and certain species of Pentaschistis Stapf. Urochlaena pusilla is very similar to Tribolium utriculosum (Nees) Renv. in leaf anatomy and these two

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47

Mardiyyaningsih, A. N., and E. Daningsih. "Preparation of leaf anatomy slide using modification protocols." IOP Conference Series: Earth and Environmental Science 976, no. 1 (2022): 012061. http://dx.doi.org/10.1088/1755-1315/976/1/012061.

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Abstract Preparing leaf anatomy slide is a routine procedure in physiology and anatomy plant research. A standard microtechnique method frequently adopted for doing such procedure is Johansens’. However, for early user such as university students, executing this method may be challenging in term of using many chemicals in different stages which make it more pricey and need longer duration. This research attempts to analyse the possibility for using simpler protocol suggested by Gunarso to replace Johansens method. It is conducted under a qualitative experiment design involving leaves from mono

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48

Smith, A. H., B. M. Potts, D. A. Ratkowsky, E. A. Pinkard, and C. L. Mohammed. "Association of Eucalyptus globulus leaf anatomy with susceptibility to Teratosphaeria leaf disease." Forest Pathology 48, no. 2 (2017): e12395. http://dx.doi.org/10.1111/efp.12395.

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49

Gould, K. "Leaf Heteroblasty in Pseudopanax crassifolius: Functional Significance of Leaf Morphology and Anatomy." Annals of Botany 71, no. 1 (1993): 61–70. http://dx.doi.org/10.1006/anbo.1993.1007.

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50

Brzezicka, E., K. Karwowska, M. Kozieradzka-Kiszkurno, and M. Chernetskyy. "Leaf micromorphology of Kalanchoë laciniata (Crassulaceae)." Modern Phytomorphology 8 (May 20, 2015): 49–52. https://doi.org/10.5281/zenodo.159829.

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The main aim of the work was to characterize morphology and anatomy of succulent leaves. Morphological and anatomical studies conducted on succulent leaves of Kalanchoë laciniata. The anatomy of leaves where studied with the use of light microscopy. This species belongs to the family Crassulaceae and it demonstrates the presence of adaptive traits which are necessary to survive and allow them inhabit in dry environment. Family Crassulaceae occur on arid and semiarid areas, among the rocks, on the sandy areas and in the mountains. Anatomical studies show that leaves of K. laciniata possess a wa

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