Carbon Dioxide Uptake of Six Plant Species Under Different Light Intensities
Article information
Abstract
Background and objective
Carbon dioxide (CO2) is a common indoor air pollutant that can lead to respiratory issues, impaired cognitive function, and increased absenteeism. Plants play a key role in CO2 absorption through the process of photosynthesis, which is influenced by light intensity. This study aimed to assess the potential of plant species for CO2 reduction under different light conditions, providing baseline data to optimize their effectiveness in improving indoor air quality.
Methods
Six plant species, including three evergreen broad-leaved plants (Pittosporum tobira (Thunb.) W.T.Aiton, Camellia japonica L., Viburnum odoratissimum Ker Gawl. ex Rümpler var. awabuki (K.Koch) Zabel ex Rümpler) and three foliage house plants (Alocasia sinuata, Monstera deliciosa, and Epipremnum aureum) were selected to evaluate their CO2 reduction ability under four different light intensities (10, 40, 80, and 160 μmol m−2 s−1). The plants were exposed to light for 11 hours, followed by a 11 hour dark period. A CO2 cylinder was used to introduce CO2 into the test chamber, and the CO2 concentration inside the test chamber was recorded every 10 minutes over a 22-hour period. Net photosynthesis was also measured for each plant species.
Results
The CO2 reduction capacity varied among plant species and light intensities. All six plant species exhibited the highest CO2 uptake at 160 μmol m−2 s−1, with uptake decreasing as light intensity decreased. Light intensity had a significant impact on the plants’ CO2 reduction ability, and CO2 absorption continued during the dark period. Among the six species, Monstera deliciosa and Epipremnum aureum demonstrated the highest CO2 uptake.
Conclusion
Plants require adequate light intensity for effective CO2 uptake, making it crucial to examine their ability to assimilate CO2, as plant species that emit CO2 can have a negative impact on health. This will help identify which plant species can absorb CO2 without raising CO2 levels, especially in indoor environments where low light conditions are common. This study offers additional insights into the CO2 absorption capacity of plants, enabling landscape researchers to select suitable species that contribute to balancing and reducing CO2 concentrations in indoor environments. Further research is necessary to determine the optimal light levels and the right plant species for enhancing CO2 reduction effects in plants.
Introduction
Because of increasing urbanization and modern lifestyles, people now spend more than 80% of their time indoors (Tran et al., 2020). As a result, indoor air quality (IAQ) has become increasingly important. Poor IAQ has numerous adverse effects on humans in both the short and long term. Increasing air pollution, including CO2, has been linked to an increased incidence of human diseases (Mannan and Al-Ghamdi, 2021; Mata et al., 2022). Exposure to indoor air pollutants such as CO2 has been associated with an increased incidence of human diseases (Moya et al., 2019).
Indoor air pollution includes particulate matter, volatile organic compounds (VOCs), and gaseous pollutants such as NOx and CO2 (Vardoulakis et al., 2020). Major sources of indoor pollution include indoor activities (such as cooking, heating, and cooling systems), building materials, and the infiltration of outdoor air pollution (Soni and Dhankar, 2019). Among these pollutants, CO2 is one of the most common indoor air contaminants (Torpy et al., 2014). CO2 concentration is commonly used as a metric to assess the level of indoor pollution. The maximum safe exposure concentration of CO2 is 1000 ppm (Moya et al., 2019). However, in environments where people are actively gathered, CO2 concentration frequently rises to 2000 to 2500 ppm (Majumdar et al., 2021). Numerous studies have demonstrated that elevated CO2 concentrations are associated with respiratory problems, reduced cognitive performance, and increased absenteeism (Liu et al., 2022). Indoor plants can effectively control and regulate CO2 levels through the process of photosynthesis (Dumont and Héquet, 2017). During photosynthesis, plants absorb CO2 and release oxygen (O2) (Armijos-Moya et al., 2022; Deng and Deng, 2018; Ravindra and Mor, 2022). Additionally, plants transpire water from their roots to their leaves, subsequently releasing it into the environment (Liu et al., 2022). Thus, indoor plants not only reduce CO2 levels but also contribute to an increase in relative humidity. However, the ability of plants to reduce CO2 varies among different plant species (Bui et al., 2024). Moreover, environmental conditions such as water, light, nutrients, and air are essential for plant growth (Madiraju et al., 2020). Among these factors, light intensity serves as the primary driver of CO2 uptake (Sugano et al., 2024). The net photosynthetic rate differs among plant species depending on light intensity (Chen et al., 2019; Hendrik and Negal, 2000; Matysiak et al., 2021).
Numerous studies have demonstrated that higher light intensities result in an increased net photosynthetic rate, thereby enhancing CO2 uptake in plants (Dominici et al., 2021; Weerasinghe et al., 2023). However, indoor light levels (photosynthetic photon flux densities of 10–50 μmol m−2 s−1) are typically much lower than the levels required for optimal plant growth and development (Weerasinghe et al., 2023). Therefore, understanding the CO2 reduction effects of indoor plants under different light levels is essential for optimizing their CO2 removal potential. This study aimed to estimate the CO2 removal effects of different plant species under varying light levels to establish baseline data that could enhance the CO2 reduction potential of plants in indoor environments. of plants in the indoor environment.
Research Methods
Study plant species
Six different plant species were selected for this study, including three evergreen broad-leaved plants (Pittosporum tobira (Thunb.) W.T.Aiton, Camellia japonica L., Viburnum odoratissimum Ker Gawl. ex Rümpler var. awabuki (K.Koch) Zabel ex Rümpler) and three foliage house plants (Alocasia sinuata, Monstera deliciosa, and Epipremnum aureum) (Table 1). All testing plant species were cultivated under the same conditions to prepare for this study. Each plant species with the same height and size was selected for this study. Then, selected plants were cultivated under different light levels (10, 40, 80, and 160 μmol m−2 s−1) for three months to help plants adapt to the different light conditions. A portable photosynthesis system (LCpro+, ADC BioScientific Ltd., UK) was used to determine the photosynthetic rate of each plant species before testing.
CO2 test chamber setup
Acrylic chambers (550 mm × 600 mm × 800 mm, L × W × H) were used to model the indoor environment. LED white light source panel emitting four light intensities corresponding with 10, 40, 80, and 160 μmol m−2 s−1 was placed on top of the test chamber to provide a light source for the study plant species. The light and dark time ratio was provided for each test chamber at 11:11 hours. All testing was conducted from February 2024 to June 2024. During this period, all test chambers were placed inside a controlled environment room, where the temperature was maintained at 25°C. All tests were conducted five times for each plant species and each light treatment. Plant species were placed simultaneously with a CO2 concentration meter at the center of the test chamber. One potted plant of each species was positioned at the center of different chambers for the test. In this study, a CO2 cylinder was used as the source of CO2. The CO2 was injected directly into the test chamber until the initial concentration of CO2 reached 1000 ppm. Indoor Air Quality Meters (IAQ-CALC Indoor Air Quality Meter model 7545, TSI Inc., USA) were used to measure the CO2 concentration inside the test chamber every 10 minutes for 22 hours (Fig. 1).
Statistical analysis
All data were analyzed using SAS software version 9.4 (SAS Institute, NC, USA) with analyses of variance (ANOVA) and Duncan’s Multiple Range Test (DMRT). The significance level was set at 5%.
Results and Discussion
CO2 reduction under a light intensity of 10 μmol m−2 s−1
The CO2 concentration in the four test chambers showed a slight decrease during the light period and increased during the dark period (Fig. 2). During the light period, the CO2 concentration increased in the three chambers and decreased in the remaining three. The net CO2 increase was highest in the chamber containing V. odoratissimum var. awabuki, with a net CO2 increase of approximately 102.60 ppm, corresponding to 10.26% of the initial 1000 ppm concentration. Chambers containing P. tobira and A. sinuata exhibited net CO2 increases of 66.80 and 42.50 ppm, equivalent to 6.68 and 4.25%, respectively. In contrast, the net CO2 concentration slightly decreased in chambers with E. aureum, C. japonica, and M. deliciosa. The largest decrease was observed in M. deliciosa (101.60 ppm, corresponding to a 10.16% reduction), followed by C. japonica (4.66 ppm) and E. aureum (2.10%). During the dark period, net CO2 increased in all test chambers, ranging from 142.20 to 190.50 ppm, equivalent to 12.44 to 27.24% of the initial concentration. The net CO2 increase exceeded the CO2 uptake capacity of all six plant species tested. After 22 hours of testing, the CO2 concentration was greater than the initial level in all chambers. The net CO2 concentration increased by approximately 12.21% to 28.42% relative to the initial concentration.
CO2 reduction under a light intensity of 40 μmol m−2 s−1
The net CO2 concentration decreased during the light period in all test chambers, except in the chamber with P. tobira (Fig. 3). Net CO2 increased from 50.20 to 362.40 ppm, corresponding to 5.02 to 36.24% relative to the initial 1000 ppm concentration. E. aureum exhibited the highest CO2 uptake, followed by M. deliciosa and A. sinuata. The lowest CO2 reduction was observed in V. odoratissimum var. awabuki, followed by C. japonica. In contrast, the net CO2 concentration in the P. tobira chamber increased by approximately 79.80 ppm, equivalent to 7.98%, during the light period. During the dark period, net CO2 concentration increased in all chambers, ranging from 120.80 to 284.80 ppm, or 12.08 to 28.48% relative to the initial concentration. Among the all chambers, A. sinuata and E. aureum exhibited the highest and lowest net CO2 increases, respectively. After 22 hours of testing, CO2 concentration decreased in the chambers containing M. deliciosa (10.14%) and E. aureum (24.48%), while it increased in the remaining chambers.
CO2 reduction under a light intensity of 80 μmol m−2 s−1
During the light period, the CO2 concentration decreased in all test chambers, while the chambers containing M. deliciosa and E. aureum showed a decrease of more than 50% compared with the initial CO2 concentration (Fig. 4). Among the six plant species, the test chamber with E. aureum exhibited the highest CO2 uptake, with a reduction of 706.20 ppm, equivalent to 70.62%, followed by M. deliciosa (62.86%), and C. japonica (41.45%). In contrast, the chamber with V. odoratissimum var. awabuki showed the lowest CO2 uptake, with a reduction of 116.20 ppm (11.62%). Similar trends were observed under other light treatments, during which the CO2 concentration increased in all test chambers. The net CO2 increases ranged from 153.00 to 359.80 ppm, corresponding to 15.30 to 35.98%. The chamber with P. tobira showed the highest net CO2 increase, followed by C. japonica and M. deliciosa, while the chamber with V. odoratissimum var. awabuki exhibited the lowest increase.
CO2 reduction under a light intensity of 160 μmol m−2 s−1
In this light treatment, the CO2 concentration inside both chambers was significantly reduced during the light period (Fig. 5). The uptake of CO2 inside the all test chambers ranged from 324.20 to 871.60 ppm, corresponding to 32.42 to 87.16% relative to the initial concentration. Among the all chambers, the highest CO2 reduction was observed in the chamber with M. deliciosa, followed by those with E. aureum and P. tobira, showing reductions of 76.15 and 75.15%, respectively. The chamber with V. odoratissimum var. awabuki exhibited the lowest CO2 reduction at 32.42%. During the dark period, a similar trend to that observed in other light treatments was found, with CO2 concentration increasing in all chambers. The net CO2 increase ranged from 310.60 to 500.20 ppm, corresponding to 31.06 to 50.2% of the initial 1000 ppm concentration. The chamber with P. tobira showed the greatest net CO2 increase, followed by C. japonica, while the chamber with E. aureum exhibited the lowest increase. After all test periods, the CO2 concentration in all chambers was lower than the initial 1000 ppm. However, the net CO2 decrease in the chamber with C. japonica and V. odoratissimum var. awabuki was only approximately 5%, showing little change from the initial concentration. In contrast, the net CO2 decrease in the chambers with E. aureum and M. deliciosa was nearly 50%, with reductions of 48.84 and 46.00%, respectively.
Photosynthesis of six plant species under different light intensities
Net photosynthesis varied among the six plant species and across different light intensities (Fig. 6). The net photosynthesis rate increased proportionally with light intensity, ranging from 10 to 160 μmol m−2 s−1. At 10 μmol m−2 s−1, net photosynthesis ranged from 0.38 to 1.74 μmol m−2 s−1. The species with the highest and lowest rates were M. deliciosa and P. tobira, respectively. At 40 μmol m−2 s−1, net photosynthesis ranged from 0.51 to 2.37 μmol m−2 s−1, with M. deliciosa again showing the highest rate, followed by E. aureum. In contrast, P. tobira maintained the lowest photosynthetic activity. At 80 and 160 μmol m−2 s−1, the net photosynthesis of six species ranged from 2.13 to 4.81 and from 4.83 to 6.06 μmol m−2 s−1, respectively. At these light levels, C. japonica and M. deliciosa exhibited the highest net photosynthetic rates. The species with the lowest rate across all intensities was V. odoratissimum var. awabuki.
Net photosynthesis rate of six plant species under different light intensities: A: 10 μmol m−2 s−1, B: 40 μmol m−2 s−1, C: 80 μmol m−2 s−1, D: 160 μmol m−2 s−1. Different letters indicate significant differences in net photosynthesis rate among the six plant species.
During photosynthesis, plants use energy from light to remove CO2 and release O2 into the atmosphere (Suhaimi et al., 2017). Many studies have demonstrated the role of different plant species in reducing CO2 from the atmosphere (Torpy et al., 2014; 2017). Nowadays, more studies have focused on CO2 removal in indoor environments such as schools, offices, and hospitals (Sevik et al., 2017). Several studies have shown that indoor plants can significantly reduce atmospheric CO2 concentrations (Dominici et al., 2021; Gubb et al., 2022; Weerasinghe et al., 2023).
Our preliminary study identified four different plant species (Neolitsea sericea, Coffea arabica, Photinia glabra, and Farfugium japonicum) as having highly effective CO2 removal capacity (Bui et al., 2024). This finding aligns with the current results, in which all six plant species tested demonstrated effective CO2 removal during the light period. Another study showed that the ability to remove CO2 varied with light intensity (Suhaimi et al., 2017). Gubb et al. (2019) reported that Dracaena fragrans ‘Golden Coast’ removed CO2 to 600 ppm under a very high light intensity of 22,000 lx. In this study, CO2 removal by all plant species increased as light intensity increased from 10 to 160 μmol m−2 s−1. Additionally, M. deliciosa reduced CO2 concentration in the chamber 370 ppm and 125 ppm under 80 and 160 μmol m−2 s−1, respectively. In the case of E. aureum, the CO2 concentration decreased to 290 ppm and 229 ppm under the same light intensity.
The light level significantly influenced plant photosynthesis, which is closely related to the CO2 reduction potential of plants (Sugano et al., 2024). Most plant species require high light intensity for efficient photosynthesis (Miao et al., 2023). Low light conditions in indoor environments are often insufficient for plant growth and development, particularly for photosynthetic activity (Gupta et al., 2016; Han and Ruan, 2020; Sugano et al., 2024). Under low light intensity, the photosynthetic rate of plants was lower than under higher light conditions (Cetin and Sevik, 2016). Other studies have indicated that plants can uptake CO2 when provided with adequate light, but they are unable to do so under insufficient light conditions (Dominici et al., 2021). This observation is consistent with the results of our study. In this study, almost all plant species exhibited no CO2 uptake under a light intensity of 10 μmol m−2 s−1.
Plant respiration is a fundamental process that complements photosynthesis, determining the net accumulation of carbon in plants and playing a vital role in the carbon balance of individual cells. (Jones et al., 2024). This process produces CO2 as a by-product (O’Leary et al., 2016). The respiration of plants depended on the species, leaf age, CO2 concentration and light intensity (Gonzalez-Meler et al., 2004; Villar et al., 1995). Under 10 μmol m−2 s−1, we suggest that all plant species emitted CO2 through respiration, which was the main reason leading to increasing CO2 in Fig. 2 and in the dark conditions of other light conditions. A similar result was observed at 40 μmol m−2 s−1. In indoor environments, such low light levels may be at or near the photosynthetic compensation point of many plant species, which may explain the limited CO2 reduction observed under 10 and 40 μmol m−2 s−1. Among the six plant species, M. deliciosa and E. aureum showed greater CO2 uptake and net photosynthesis rates than others under 40 μmol m−2 s−1. We suggest that their greater acclimatization to low light levels may be a key factor contributing to their higher CO2 uptake. Many plant species possess physiological mechanisms that allow them to adapt to low light conditions and maintain photosynthesis for growth and development (Liu et al., 2022). Torpy et al. (2017) reported that E. aureum and three other plant species maintained efficient photosynthesis under 6.8 μmol m−2 s−1. This plant species also exhibited the highest CO2 uptake under the 80 and 90 μmol m−2 s−1.
In this study, M. deliciosa and E. aureum were the most effective species for CO2 reduction. In contrast, C. japonica and V. odoratissimum var. awabuki showed the lowest CO2 reduction across all light levels, and P. tobira also exhibited low CO2 reduction at all intensities except 160 μmol m−2 s−1. This study further found that the three woody species showed lower CO2 uptake efficiency than the three herbaceous species. Although the net photosynthesis rate of woody species was higher, this result suggests that CO2 uptake is influenced by multiple factors beyond photosynthesis, including species-specific characteristics. Deng et al. (2022) also indicated that herbaceous plants are better suited than woody plants to achieve rapid carbon fixation. In addition to environmental conditions, inherent traits of plant species must be considered when selecting species for indoor CO2 reduction (Honour et al., 2009; Mulenga et al., 2020; Zheng et al., 2018). All six plant species emitted CO2 during the dark period, although the rate of emission varied among species and was influenced by light intensity. Under low light conditions, CO2 emission sometimes exceeded uptake, indicating that some plants may become net CO2 producers under such conditions. Therefore, the careful selection of plant species is essential to maximize the CO2 reduction potential in indoor environments.
Conclusion
In this study, six plant species effectively removed CO2, and the ability to remove CO2 varied among species and across different light intensities. The CO2 reduction potential of all six species increased with rising light intensity and was highest at 160 μmol m−2 s−1. The three woody species exhibited lower CO2 reduction efficiency than the three herbaceous species, and a similar trend was observed in their net photosynthetic rates. The species that demonstrated the highest CO2 removal efficiency were M. deliciosa and E. aureum, compared to the other species tested. Under low light conditions (10 and 40 μmol m−2 s−1), CO2 emissions exceeded CO2 uptake, indicating a net release of CO2. Plants require suitable light intensity to ensure CO2 uptake, so studying their ability to assimilate CO2 is essential for determining which plant species can effectively absorb CO2 without enhancing its levels, particularly in indoor environments where low light conditions often prevail. This study provides additional insights into the CO2 absorption capacity of plants, enabling landscape researchers to select suitable plants that contribute to balancing and reducing CO2 concentrations in indoor environments. Therefore, selecting appropriate plant species is crucial for enhancing CO2 reduction and improving indoor environmental quality. Further research is needed to determine optimal light conditions and suitable species for maximizing the CO2 reduction capacity of indoor plants.
Notes
This work was carried out with the support of the “Cooperative Research Program for Agriculture Science and Technology Development (Project No. Rs-2022-RD010280)”, Rural Development Administration, Republic of Korea.