The Relationship between Thickness of Tissues of CAM Plants and Light, Temperature, Water, Gas Pressure and CAM Acid

2021-05-27 23:59:12
5 pages
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University of Richmond
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Dissertation introduction
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CAM plants (Crassulacean Acid Metabolism) is a special type of carbon pathway that was attained through evolution in some plants. Such plants have special characteristics such stomata closure during the day while it opens during the night (Monteiro et al. 2016). The adaptation enables the plants to reduce water loss through evapotranspiration. CAM plants stores Carbon (IV) Oxide as malate (four-carbon acid compound, the acid is stored at night in vacuoles of the leaf and the other green parts of the plant like the stem and exposed roots (Habibi & Ajory, 2015). The stored malate is later used during the day in the RuBisCO circle where CO2, this increase the efficiency of photosynthesis in CAM plants (Monteiro et al. 2016). Succulence or rather thickness of the CAM plant is one of the greatest advantages that the plant has towards it photosynthetic pathway. The paper intends to discuss how the thickness of CAM plants tissues and acid metabolism relates to water, temperature and gas pressure.

Temperature and Thickness of Tissues

Temperature is a crucial element in plant metabolism; plants require moderate temperatures to conduct their daily metabolic activities. However, CAM plants are plants that thrive in hot and dry areas hence they have unique adaptations to survive in such areas, one of the adaptation is being succulent (Aragon et al. 2013). Therefore, CAM plants have thick tissues; the thick leaves enable the plans to preserve water. The thickness of the leaves and stem is thus a special adaptation that enables the plant to survive in areas with a limited amount of water (Habibi & Ajory, 2015). Thus, the high temperature increases the level at which CAM plant tissues are thick (succulent) the thick tissues stores water to counter limited supply in an ecosystem.

Water and Thickness of Tissues

Water is an essential requirement for plant growth and metabolic activities. CAM plants are plants that are adapted to survive in dry areas. Therefore, the plants necessitate adaptations that will enable it to survive in water deficient ecosystem. The plants have developed and evolutionary mechanism which enables it to store water. The mechanism has thick fleshy tissues. An example is a pineapple; pineapples have a fleshy stem and leaves (Aragon et al. 2013). The thick stem and leaves are adapted to store water for survival in arid conditions. Aloe Vera is another example of a CAM plant with succulent leaves (thick leaves) which are for water storage (Davis et al. 2014). The thickness of the leaves is, therefore, a special adaptation that enables the CAM plants to survive in arid ecosystems. Leaf and stem thickness enhances water storage capacity of the CAM plants in arid areas. Studies have proven that CAM plants with thicker tissues have a higher chance of surviving in water deficient areas that those with less thick tissues.

Light and Thickness of Tissues

Light is essential for the process of the photosynthesis to take place in plants, without light photosynthesis is impossible. The leaves of most CAM plants are thick but have chlorophyll which attracts light for photosynthesis. Thickness enables the leaves to store water and other chemicals such as abscisic acid that enables the plant to close the stomata during the day (Aragon et al. 2013). Zeaxanthin is also a chemical that most CAM plants store in the thick layers of the guard cells combination of Abscisic acid prevents the stomata opening during the day and allows accumulation of carbon during the night (Kuzniak et al. 2016). Thick leaves allow light to penetrate and concentrate on the plants hence making the decarboxylation process manageable during the day.

Gas Pressure and Thickness of Tissues

CAM plants are adapted to fix carbon during the night and utilize the fixed carbon during the day. The carbon fixed is gained from carbon (IV) oxide through the stomata (Ren et al. 2015). Carbon (IV) oxide enters the stomata with the aid of pressure differences between the internal structures of the stomata and the external environment. Thick leaves have thick cells that have the potential of generating high pressure for gaseous exchange during the night. For CAM plats to attain efficiency in carbon fixation at night, the pant must take in as much carbon from the air as possible. The thickness of the tissues is an adaptation that enables the plants to sustain the pressure needed for intake of carbon (iv) oxide and exit of oxygen released in the decarboxylation process in the leaves during the photorespiration process (Scalisi et al. 2016). Oxygen is a byproduct of photorespiration it needs sufficient pressures for it to be released at the rate that carbon is being absorbed. The thickness of the leaves tissues provides the needed pressure for gaseous pressure in CAM plants.

CAM Acid

CAM acid like the malic acid needs storage tissue that can hold them for long before decarboxylation, thick tissues of the leaves and fleshy stem provide such storage facilities in CAM plants (Habibi & Ajory, 2015). The thickness of the tissues is thus an added advantage for the survival of the CAM plants in arid areas (Robert et al. 2014).

Conclusion

CAM plants are special plants adapted to survive in water deficient areas; the plant has several features that enable it to survive in such environments. One of the significant adaptations noted is the succulence or the thickness of its tissues. The thickness of CAM plants tissues enables it to survive arid conditions as noted in the paper.

 

References

Ren, J., Cai, B., He, X., Yao, H., Du, S., & Shang, F. (2015). The Relationship between Stomatal Movement and Light Intensity Gradient in Three Dendrobium Species Compared with Typical CAM Plants. Agricultural Biotechnology, 4(2), 28.

Davis, S. C., LeBauer, D. S., & Long, S. P. (2014). Light to liquid fuel: theoretical and realized energy conversion efficiency of plants using Crassulacean Acid Metabolism (CAM) in arid conditions. Journal of experimental botany, 65(13), 3471-3478.

Aragon, C., Pascual, P., Gonzalez, J., Escalona, M., Carvalho, L., & Amancio, S. (2013). The physiology of pineapple (L. Merr. var MD-2) as CAM or C3 is regulated by the environmental conditions: proteomic and transcriptomic profiles. Plant Cell Reports, 11(32), 1807-1818.

Scalisi, A., Morandi, B., Inglese, P., & Bianco, R. L. (2016). Cladode growth dynamics in Opuntia ficus-indica under drought. Environmental and Experimental Botany, 122, 158-167.

Kuzniak, E., Kornas, A., Kazmierczak, A., Rozpadek, P., Nosek, M., Kocurek, M., ... & Miszalski, Z. (2016). Photosynthesis-related characteristics of the midrib and the interveinal lamina in leaves of the C3CAM intermediate plant Mesembryanthemum crystallinum. Annals of Botany, mcw049.

Robert, C. A., Ferrieri, R. A., Schirmer, S., Babst, B. A., Schueller, M. J., Machado, R. A., ... & Erb, M. (2014). Induced carbon reallocation and compensatory growth as root herbivore tolerance mechanisms. Plant, cell & environment, 37(11), 2613-2622.

Heyduk, K., McKain, M. R., Lalani, F., & Leebens-Mack, J. (2016). Evolution of a CAM anatomy predates the origins of Crassulacean acid metabolism in the Agavoideae (Asparagaceae). Molecular Phylogenetics and Evolution, 105, 102-113.

Habibi, G., & Ajory, N. (2015). The effect of drought on photosynthetic plasticity in Marrubium vulgare plants growing at low and high altitudes. Journal of plant research, 128(6), 987-994.

Aragon, C., Pascual, P., Gonzalez, J., Escalona, M., Carvalho, L., & Amancio, S. (2013). The physiology of ex Vitro pineapple (Ananas comosus L. Merr. var MD-2) as CAM or C3 is regulated by the environmental conditions: proteomic and transcriptomic profiles. Plant Cell Reports, 32(11), 1807-1818.

Silva, H., Sagardia, S., Ortiz, M., Franck, N., Opazo, M., Quiroz, M., ... & Tapia, C. (2014). Relationships between leaf anatomy, morphology, and water use efficiency in Aloe vera (L) Burm f. as a function of water availability. Revista Chilena de Historia Natural, 87(1), 1.

Castillo, R. J., Cervera, J. C., & Navarro-Alberto, J. (2016). Drought and extreme temperature tolerance for Tillandsia dasyliriifolia, an epiphytic bromeliad from the northern coastal dune scrubland in Yucatan, Mexico. Botanical Sciences, 94(1), 121-126.

Tan, C. L., Wong, N. H., Tan, P. Y., Jusuf, S. K., & Chiam, Z. Q. (2015). Impact of plant evapotranspiration rate and shrub albedo on temperature reduction in the tropical outdoor environment. Building and Environment, 94, 206-217.

Monteiro, M. V., Blanusa, T., Verhoef, A., Hadley, P., & Cameron, R. W. (2016). Relative importance of transpiration rate and leaf morphological traits for the regulation of leaf temperature. Australian Journal of Botany, 64(1), 32-44.

 

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