Disclaimer: This is an example of a student written essay.
Click here for sample essays written by our professional writers.

Any scientific information contained within this essay should not be treated as fact, this content is to be used for educational purposes only and may contain factual inaccuracies or be out of date.

Investigating the Influence of Light Intensity and CO2 Concentrations on the Growth Rate of Eruca sativa

Paper Type: Free Essay Subject: Biology
Wordcount: 2271 words Published: 18th May 2020

Reference this

Investigating the Influence of Light Intensity and CO2 Concentrations on the Growth Rate of Eruca sativa


The current evidence for climate change is unequivocal. A scientific consensus has been reached that “human activities are the primary driver of global climate change” (Linden et al. 2015, Anderegg et al. 2010). However, despite this agreement among scientists, uncertainties present themselves as research is conducted into the ecosystem’s response to climate change, specifically, how the growth rates of plants are influenced by the changing environment.

Get Help With Your Essay

If you need assistance with writing your essay, our professional essay writing service is here to help!

Essay Writing Service

It is well known that even in constant environmental conditions, relative growth rates of plants can vary considerably among species (Grime & Hunt, 1975). Thus, in a shifting global environment, the need to understand the impacts that environmental conditions will have on growth rates becomes vital. However, there has been a noticeable gap in knowledge regarding the long-term effects of global climate change on agricultural productivity, with crop yield changes at the forefront of these uncertainties (Adams et al. 1998). Many species of plants are yet to be studied to observe the influence of climate change on their growth rates. Understanding this influence will begin to set the foundations for the adaptation of crop farming in the future.

Currently, research has shown that crops are extremely vulnerable to climate change (Nelson et al. 2009), most noticeably through atmospheric CO2 and light concentrations. Interestingly, the mechanisms for allowing CO2 to diffuse into the plant – the opening of the stomata – and the absorbance of light interact with each other. Thus, as the average atmospheric CO2 concentration is expected to increase, the interaction between light and CO2 is suspected to vary (Murray, 2006). This study hypothesises that if the concentration of atmospheric CO2 is increased, then the rate of photosynthesis is expected to increase accordingly. Similarly, if the amount of light intensity is increased, then the rate of photosynthesis is also expected to increase.

These variables will be compared via the growth rates of Eruca sativa leaves grown in climate-controlled conditions, aiming to provide a cursory glance into the impact of climate change on plant growth.


Influence of varied light conditions on surface area of leaves

Light conditions were varied while maintaining the atmospheric CO2 concentrations – ambient level (400ppm) – and graphed against the average surface area of E. sativa leaves (fig. 1). A noteworthy observation is the significant difference in standard errors between high and low light conditions (SEHigh = 1.2, SELow = 0.89). The results of the t-tests show a significant difference between the 2 light treatments (t = 5.44, d.f. = 198, p = 1.52 x10-7).  

Fig. 1 Influence of varied light conditions on average surface area of leaves, in cm2 with SE bars.

Influence of varied CO2 concentrations on surface area of leaves

Atmospheric CO2 concentrations were varied while maintaining a stable light condition – high level (800µmol m2s1) – and graphed against the average surface area of E. sativa leaves (fig. 2). It should be noted that the percentage difference between the average leaf surface area in the CO2 treatments is less than the difference found in the light treatments. Finally, the results of the t-tests do show a significant difference between the 2 CO2 treatments
(t = 4.90, d.f. = 198, p = 1.95 x10-6).  


Fig. 2 Influence of varied CO2 concentrations on average surface area of leaves, in cm2 with SE bars.


The results display a direct correlation between an increase in light conditions and atmospheric CO2 concentrations with a relative increase in the average leaf surface area of the E. sativa plant. The high light growing condition provides a growth rate of approximately 1.3x the ambient light condition, while a 1.2x growth rate was identified in the high CO2 vs ambient concentration. These results are thus in full support of the initial hypotheses with both sections of the experiment showing significant differences through the statistical analyses (p < 0.05). Through additional analysis, it is evident that there is a higher statistical correlation between the average surface area of leaves and the increased light conditions.

Find Out How UKEssays.com Can Help You!

Our academic experts are ready and waiting to assist with any writing project you may have. From simple essay plans, through to full dissertations, you can guarantee we have a service perfectly matched to your needs.

View our services

This result was observed by a previous study conducted on plant growth responses to light, temperature and CO2 (Hayman, 1974). The study used a highly similar method to the one used in this study, that is, growing plants in highly controlled conditions then measuring the dry weight of leaves. Hayman (1974, p. 71) concluded that the highest light conditions “simulated growth to the same extent as the addition of soluble phosphate” – a fertilizer that improved plant growth significantly – supporting the results of this experiment.

In a biological context, this highlights that the amount of light available to E. sativa holds more influence on the growth rate than the CO2 concentration. Further, this implies that in an agricultural setting, it is more beneficial to grow crops that are similar to E. sativa in areas of high light due to the noticeable surface area differences observed (Fig. 1). A high crop yield would thus be expected when utilising this growing condition. The results also show that a high CO2 concentration would be beneficial, however, this growing condition is significantly harder to control and maintain than searching for areas of high light.

Another study conducted in 2016 provides an alternative approach to understanding the interaction between light intensity, CO2 concentration and growth rate. By investigating the variables that limit plant growth, this study identified components with the strongest control over growth in major crops (White et al. 2016). Elevated CO2 concentrations were found to stimulate photosynthetic rates, which typically translates into faster growth. However, a certain trade-off exists, in that, the acclimation of photosynthetic rates could not be achieved without defoliation due to the limiting factor of light (Bryant et al. 1998, as cited in White et al. 2016). Despite the differences in methodology and investigation, this supports the results of this study, highlighting that while elevated atmospheric CO2 concentrations will positively impact photosynthetic rates, light intensity is still necessary for the translation into faster growth.

Evidently, from the results of this study and others, conclusions can be drawn about the short-term impacts of variable conditions on the growth rate of E. sativa plants. However, an obvious limitation of this study is the lack of ability in observing impacts over longer time periods – the main reason being the economic sustainability of the study. To critically analyse the viability of crop farming in future environments, gathering data over substantial periods of time in order to extrapolate with accuracy is essential (Adams et al. 1998, Nelson et al. 2009). Studies to rectify this limitation have been carried out, depicting logarithmic relationships between growing conditions and plant growth, suggesting that after a certain increase in either light intensity or CO2 concentration, photosynthetic rates will begin to plateau (Eilers & Peeters, 1998). This is due to the plant reaching the point of maximum CO2 fixation.

This however, highlights another limitation in the methodology of this study – an inability to observe the rate of plant growth. This study restricts itself to the results of each growing condition and not the rate at which E. sativa grows. In the future, this study could be improved by taking photosynthetic measurements for each plant in each growing condition with a portable photosynthesis system – very similar to the method used by Eilers and Peeters (1998). Measurements should be taken daily for the duration of the study to allow for the comparison of growth rates as well as the final leaf surface area. This would enable a progressive study of plant growth changes correlated with the changing climate.

A third and final limitation of this study concerns the accuracy of the measurements being taken, namely, the surface area of the selected E. sativa leaves. Leaf surface area is naturally expected to increase at a rate that is correlated with the growth of the plant. However, while this may be true for overall photosynthetic levels, net photosynthesis per leaf weight is actually found to decrease with increasing light intensity (B. Chabot & J. Chabot, 1997). This observation was attributed to a massive starch accumulation in the chloroplasts which slows the photosynthesis process. Although this observation does not present itself significantly in the current study, the systematic error still exists. In the future, a more accurate method for measurement of plant growth is required – possibly an average of multiple measurement techniques including leaf thickness, density and mesophyll cell surface area. Using multiple measurements in the methodology will reduce errors and allow for more accurate data to be collected in future studies.

This study aimed to investigate the influence of climate change on the growth rate of E. sativa plants via the environmental variables of light intensity and atmospheric CO2 concentration. This study has identified that despite CO2 being a controlling factor in plant growth, light intensity holds the most influence over growth. These results were highlighted as being short-term findings, with more research required to understand the long-term sustainability of crop farming in our society. However, in the immediate term, farmers can begin to expect higher crop yields due to our changing climate.

Reference List

  • Adams RM, Hurd BH, Lenhart S, Leary N 1998, ‘Effects of Global Climate Change on Agriculture: An Interpretative Review’, Climate Research 11(1), pp. 19-30. Available from: https://www.int-res.com/abstracts/cr/v11/n1/p19-30/
  • Anderegg WRL, Prall JW, Harold J, Schneider SH 2010, ‘Expert Credibility in Climate Change, PNAS 107(27), pp. 107-109. DOI 10.1073/pnas.1003187107
  • Chabot BF, Chabot JF 1997, ‘Effects of Light and Temperature on Leaf Anatomy and Photosynthesis in Fragaria vesca’, Oceologia 26(4), pp. 363-377. DOI 10.1007/BF00345535
  • Cook J, Nuccitelli D, Green SA, Richardson M, Winkler B, Painting R, Way R, Jacobs P, Skuce A, ‘Quantifying the Consensus on Anthropogenic Global Warming in the Scientific Literature’, Environmental Research Letters 8(2). DOI 10.1088/1748-9326/8/2/024024
  • Eilers PHC, Peeters JCH 2003, ‘A Model for the Relationship Between Light Intensity and the Rate of Photosynthesis in Phytoplankton’, Ecological Modelling 42(3), pp. 199-215. DOI 10.1016/0304-3800(88)90057-9
  • Field, CD 1995, ‘Impact of Expected Climate Change on Mangroves’, Developments in Hydrobiology 106(1), pp. 75-81. DOI 10.1007/978-94-011-0289-6_10
  • Grime JP, Hunt R 1975, ‘Relative Growth-Rate: Its range and adaptive significance in a local flora’, Journal of Ecology 63(2), pp. 393-422. DOI 10.2307/2258728
  • Hayman DS 1973, ‘Plant Growth Responses to Vesicular-arbuscular Mycorrhiza: VI. Effect of Light and Temperature’, New Phytologist 73(1), pp. 71-80. DOI 10.1111/j.1469-8137.1974.tb04607.x.
  • Magness JR 1920, ‘Effect of Light Intensity on Plant Growth’, Botanical Gazette 70(3), pp. 246-248. Available from https://www.jstor.org/stable/2470260.
  • Murray D 1996, ‘Plant Responses to Carbon Dioxide’, American Journal of Botany 82(5), pp. 690-697. DOI 10.2307/2445426
  • Nelson, GC, Rosegrant, MW, Koo, J, Robertson, R, Sulser, T, Zhu, T, Ringler, C, Msangi, S, Palazzo, A, Batka, M, Magalhaes, M, Valmonte-Santos, R, Ewing, M, Lee, D 2009, Climate Change: Impact on Agriculture and Cost of Adaptation, Intl Food Policy Res Inst, New York, NY.
  • Linden SL, Leiserowitz AA, Feinberg GD, Maibach EW 2015, ‘The Scientific Consensus on Climate Change as a Gateway Belief: Experimental Evidence’, PLoS ONE 10(2). DOI 10.1371/journal.pone.0118489.


Cite This Work

To export a reference to this article please select a referencing stye below:

Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.

Related Services

View all

DMCA / Removal Request

If you are the original writer of this essay and no longer wish to have your work published on UKEssays.com then please: