Skip to main content

Low CO2 concentration, a key environmental factor for developing plateau adapted rapeseed

Abstract

Background

Photosynthesis is a fundamental process that underlies the formation of crop yield, wherein light serves as the driving force and carbon dioxide (CO2) as the raw material. These two factors have a direct influence on the progress and efficiency of photosynthesis in crops. Rapeseed is one of the four major oilseed crops worldwide. Plateau rapeseed has now become a research hotspot. However, the lack of high-yielding rapeseed germplasm resources on the plateau and the highly efficient strategy for screening them severely affect the development of rapeseed industry in plateau.

Results

In the rapeseed experimental fields located on the plateau (Lhasa, Tibet), we measured abundant sunlight, characterized by an average daily photosynthetically active radiation (PAR) of 1413 μmol m−2 s−1. In addition, the atmospheric CO2 concentrations range from 300 to 400 ppm, which is only two-thirds of that in the plain (Chengdu, Sichuan). We found that under different measurement conditions of light intensity and CO2 concentration, different rapeseed genotypes showed significant differences in leaf photosynthetic efficiency during the seedling stage. Moreover, the rapeseed materials with high photosynthetic efficiency under low CO2 concentrations rather than high light intensity, exhibited significant advantages in biomass, yield, and oil content when cultivated on the plateau, indicating that the CO2 is the key environmental factor which limited rapeseed production in plateau. Based on photosynthetic efficiency screening under low CO2 concentrations, six rapeseed varieties SC3, SC10, SC25, SC27, SC29 and SC37, shown significantly higher yields in plateau environment compared to local control variety were obtained. In addition, the adaptability of rapeseed to plateau was found to be related to the activities of key Calvin cycle enzymes and the accumulation of photosynthetic products.

Conclusions

This study established a screening strategy for plateau high-yielding rapeseed materials, obtained six varieties which were suitable for plateau cultivation, explored the mechanism of rapeseed response to the plateau environment, and thus provides a feasible strategy for plateau-adapted rapeseed breeding.

Background

As the world’s fourth largest oilseed crop, rapeseed is versatile and serves as an important source of edible oil, industrial fuel and feed [1]. Rapeseed is widely cultivated worldwide and is a key component of the agricultural system in many countries. China, Canada, India, European countries (particularly France, Germany and the United Kingdom) and the United States are the major producers of oilseed rape (Fig. 1). Demand for rapeseed is increasing as the world's population continues to grow, arable land continues to decline and the energy needs of industrial development continue to rise. However, the growth and yield of rapeseed is easily affected by climate and environmental conditions. The low-altitude plains have a mild climate suitable for large-scale rapeseed cultivation, and the terrain is flat, which facilitates mechanized harvesting. However, in the plateau region, the rapeseed industry faces the lack of germplasm resources, a low level of mechanization, and an urgent need to increase yield and quality due to the unique climatic ecological environment [2]. Since the plateau region has a vast land area and abundant sunlight resources, effective use of the potential agricultural resources of the plateau region, selection and breeding of new high-yielding rapeseed varieties suitable for growing on the plateau is crucial for improving global oilseed rape production, promoting the development of global agricultural production, and ensuring food and oil security.

Fig. 1
figure 1

Distribution and production of rapeseed in the world in 2021, with data from the Food and Agriculture Organization of the United Nations (FAO)

Photosynthesis serves as the physiological foundation for crop yield formation, with 90–95% of a plant's dry matter directly from photosynthesis [3]. In recent years, numerous studies have shown that photosynthetic efficiency, a key factor influencing crop growth and yield, exerts a significant impact across various crops, environmental conditions, and growth stages. The variances in leaf photosynthetic effectiveness may account for crop yield disparities observed among different varieties [4], with high photosynthetic efficiency crops having an obvious yield advantage [5]. It has been reported that biotechnology-based enhancements of light protection mechanisms in tobacco resulted in an increased leaf photosynthesis rate, leading to a notable 15% rise in biomass yield [6]. The increase in wheat yield is associated with higher leaf photosynthesis rate and stomatal conductance [7]. In addition, decreased yield of rice [8], maize [9], and potatoes [10] has been reported as a consequence of covariantized photosynthesis under stress conditions. Net photosynthetic rate of different rapeseed genotypes was either significantly different or positively correlated with the yield per plant at all reproductive stages [11]. Therefore, enhancing rapeseed's light energy utilization and selecting high photosynthetic efficiency germplasm resources are crucial for boosting rapeseed yield in the plateau region, building on existing agricultural practices.

The efficiency of photosynthesis in crops is influenced by several factors, with light intensity and carbon dioxide concentration being the important environmental factors affecting photosynthesis. Studies have shown that low light intensity has a significant negative impact on soybean leaf weight, stomatal density, and photosynthesis [12]. Low light intensity conditions limit the synthesis of photosynthetic products in the whole growth period of rice, leading to yield reduction [13]. C3 plant leaves reach saturation at the light intensity of 800–1600 µmol m−2 s−1, meaning that the photosynthetic rate no longer increases with increasing light intensity [14]. CO2 is the raw material for plant photosynthesis. When the CO2 concentration reaches 700 ppm the photosynthetic rate of radish leaves increases by 20–28% compared to 400 ppm, with a dry weight increase of approximately 27% [15]. Elevated CO2 concentration significantly increases wheat photosynthetic rate, stomatal resistance, and water use efficiency [16].

Enzyme activity is also a key factor limiting crop photosynthetic efficiency. Rubisco catalyzes the fixation of CO2. However, Rubisco is a bifunctional enzyme, involved in both carboxylation of CO2 and photorespiration [17]. Therefore, the activity of ribulose-1,5-bisphosphate carboxylase (RuBPcase) has a limiting effect on carbon assimilation in C3 plants. Moreover, Rubisco needs to be activated by Rubisco activase (RCA) to function. Increasing the content of RCA without reducing Rubisco content can increase rice yield under high-temperature stress [18]. Sedoheptulose-1,7-bisphosphatase (SBPase) is involved in the regeneration of RuBP. Increased SBPase activity provides advantages in terms of carbon fixation and tolerance to oxidative stress induced by chilling in tomato plants [19]. Co-expression of SBPase and Rubisco can improve photosynthetic rate in rice [20]. Carbonic anhydrase (CA) catalysis the reversible reaction between CO2 and HCO3, reducing the diffusion resistance of CO2 in the chloroplasts and providing the substrate CO2 for the carboxylation reaction, which affects the magnitude of the photosynthetic rate of the plant [21]. Phosphoenolpyruvate carboxylase (PEPCase) fills the tricarboxylic acid cycle by supplementing oxaloacetate in C3 plants, is involved in the synthesis of organic acids, and is associated with the remobilization of CO2 [22]. Meanwhile, photosynthesis is the major carbon metabolic pathway in plants, converting CO2 from the atmosphere and H2O into organic compounds, providing energy and a carbon source for plants [23]. Soluble sugars and starch are the main forms of carbon storage in plants. Increasing carbohydrate production and recycling in source organs is an important measure for achieving high crop yields [24]. Photosynthesis not only affects carbohydrate synthesis but also impacts other pathways related to carbon metabolism. For example, the supply of photosynthetic products can regulate nitrogen metabolism, lipid metabolism, and more.

At present, with global climate warming and an increasing greenhouse effect, most studies mainly focus on the relationship between elevated CO2 concentration and crop yield, neglecting the unique ecological conditions in plateau regions with low atmospheric CO2 concentration, which also affect crop yield. Taking the Qinghai–Tibet Plateau and the Western Sichuan Plateau in China as examples, the average annual solar radiation in these regions is about two to three times that of the same latitude [25]. While the atmospheric CO2 concentration in these plateau regions is about 300 ppm [26], regions at the same latitude but lower altitude have reached 412 ppm, showing a yearly increasing trend [27]. In addition, the plateau region has a complex terrain, inconvenient transportation and low labor. Within the limited agricultural production time, people prefer to cultivate food crops, resulting in the unbalanced development of food and oil in the plateau region and the slow development of the rapeseed industry. Therefore, it is both practically and theoretically significant to study the key factors limiting yield improvement of rapeseed in the plateau region. This includes enhancing plant breeding for these limiting factors, shortening the rapeseed breeding period in the plateau, and establishing an effective screening system for advantageous rapeseed varieties. The aim is to create new materials with high photosynthetic efficiency and high-yield rapeseed in the plateau.

This study compared environmental factors in rapeseed cultivation areas on the Tibetan Plateau and the Chengdu Plain to explore non-biological factors that may limit rapeseed yield improvement on the plateau. We compared the differences in photosynthetic rate among 40 rapeseed (Brassica napus L.) varieties under different measurement conditions and identified rapeseed varieties with high photosynthetic efficiency under various conditions. Furthermore, by integrating the differences in photosynthetic parameters, growth status, agronomic traits, and seed quality of high-photosynthesis genotypes grown in the Tibetan region, we elucidated the key environmental factor affecting rapeseed production on the plateau. We successfully obtained new high photosynthetic rate and high-yield rapeseed genotypes suitable for plateau conditions. In addition, by analyzing and comparing changes in the activity of key enzymes in the Calvin cycle, photosynthetic product content, and seed fatty acid composition in rapeseed under plateau environments, we delved into the molecular mechanisms through which high-photosynthesis genotypes of rapeseed respond to the unique ecological environment of the plateau. Our research aims to establish methods for optimizing the photosynthesis process to increase yield, thereby contributing to edible oil security and sustainable agriculture in the plateau regions.

Results

Differences in environmental factors

Despite sharing a similar latitude, Lhasa and Chengdu exhibited obvious differences in various environmental factors, including sunlight intensity, temperature, humidity, and atmospheric CO2 concentration, due to their substantial altitude contrast of 4000 m (Fig. 2). During the rapeseed seedling stage, the photosynthetically active radiation (PAR) in Chengdu was significantly lower than in Lhasa. The average daily PAR in Lhasa was approximately 1413 μmol m−2 s−1, peaking at 1900 μmol m−2 s−1. Chengdu had an average daily PAR of 817 μmol m−2 s−1, with the peak at 14:30 and the maximum PAR of 1153.3 μmol m−2 s−1. The average daily temperature in Lhasa was around 30 °C, while Chengdu averaged 25 °C. Both regions had air humidity levels ranging between 30% and 40%. However, there was a significant difference in atmospheric CO2 concentration between the two regions. The average atmospheric CO2 concentration in the in Lhasa was less than 400 ppm, about two-thirds of the concentration in Chengdu.

Fig. 2
figure 2

Daily variation curves of environmental factors in the experimental bases of the Academy of Agriculture and Animal Husbandry in Lhasa, Tibet, and the Chengdu rapeseed plantation, Sichuan University, China. A Diurnal variation of photosynthetically active radiation, B diurnal variation of ambient temperature, C diurnal variation of atmospheric relative humidity, D diurnal variation of atmospheric carbon dioxide concentration

Identification of candidate rapeseed varieties with high photosynthetic efficiency

Different genotypes of B. napus exhibited significant differences in photosynthetic characteristics under different conditions (Additional file 1: Tables S1–S3). When the chamber light intensity was set to 1500 μmol m−2 s−1 and CO2 concentration was 300 μmol mol−1, the net photosynthesis rate (An) of B. napus leaves ranged from 3.01 to 22.63 μmol CO2 m−2 s−1. Among the 40 materials tested, SC3, SC10, SC25, SC27, SC34, and SC37 showed significantly higher photosynthetic efficiency compared to other materials, while SC6, SC24 and SC32 showed significantly lower photosynthetic efficiency (Fig. 3A). Under measurement conditions with the light intensity of 1000 μmolm−2 s−1 and CO2 concentration of 300 μmolmol−1, different genotypes of rapeseed showed leaf An values ranging from 2.27 to 16.11 μmol CO2 m−2 s−1. Among these materials, SC3, SC10, SC18, SC22, SC25, SC27, SC29, SC31 and SC37 showed higher leaf photosynthetic rate, while SC24 and SC32 had lower rate (Fig. 3B). When the chamber light intensity was set at 1500 μmol m−2 s−1 and CO2 concentration matched the atmospheric CO2 concentration (greater than 500 μmolmol−1), the photosynthetic rate of the leaves increased compared to the condition where CO2 concentration was 300 μmol mol−1, and the An ranged from 19.32 to 35.06 μmolCO2 m−2 s−1, with the photosynthetic rate of variety SC6 and SC26 being significantly higher than other varieties (Fig. 3C).

Fig. 3
figure 3

Net photosynthetic rate of different genotypes of Brassica napus at the following conditions A PAR:1500 μmol m−2 s−1, CO2: 300 μmol mol−1 B PAR: 1000 μmol m−2 s−1, CO2: 300 μmol mol−1 C PAR: 1500 μmol m−2 s−1, CO2: 500–600 μmol mol−1. Data shown are the means ± SE from three experimental replicates (n = 14, five plants per one experimental replicate). Different letters denote significant differences from multiple comparison test (P < 0.05) conducted for each measure condition

Adaptation of rapeseed to plateau environment

Photosynthetic parameters, biomass and yield

To further confirm the adaptability of B. napus varieties with high photosynthetic efficiency to the plateau environment, we measured the photosynthetic parameters of these materials at the rapeseed cultivating base of the Lhasa Academy of Agricultural and Livestock Sciences (Additional file 1: Table S4). An of SC6, SC24 and SC32 leaves were lower under plateau environments, and An of SC6 was only 4.62 μmol CO2 m−2 s−1, while that of SC25 was 32.11 μmol CO2 m−2 s−1. Meanwhile, the An of SC3, SC10, SC25, SC27, SC29 and SC37 showed higher photosynthetic efficiency compared to Tibetan variety Zangyou12. (Fig. 4A).

Fig. 4
figure 4

Differences in leaf net photosynthetic rate (A), yield per plant (B), biomass (C) and seed oil content (D) of various genotypes Brassica napus under plateau conditions in Tibet. Different letters indicate significant differences between different rapeseed genotypes. (P < 0.05)

In the plateau environment, high photosynthetic efficiency materials (SC3, SC10, SC25, SC27, SC29, and SC37) showed significantly higher yield per plant compared to other varieties, while there was no significant difference in yield per plant in the plain environment (Additional file 1: Table S5). Among them, the yield per plant of SC25 reached 34.25 g, approximately four times that of Zangyou12. (Fig. 4B). SC25 had 85% and 88.8% higher yield per plant than SC24 and SC32, respectively. SC27 had a grater biomass while SC6, SC24 and SC32 materials had less biomass than the other genotypes (Fig. 4C). Oil content is an important index for assessing the economic value of rapeseed. In the plateau environment, the oil content of SC3 seeds was 41.44%, SC25 was 46.87%, and SC6 was lower than other materials with only 33.31% (Fig. 4D). While in the Chengdu plain, there was no significant difference in seed oil content among them (Additional file 1: Table S5).

Plant growth and agronomic traits

Agronomic traits are statistically important in crop breeding. Therefore, observations of growth state (Fig. 5) and agronomic traits (Table 1) were conducted for different genotypes of B. napus cultivated in Tibet during the mature stage. Correlation analysis indicated a significant positive correlation between the An at the seedling stage and the number of siliques and yield per plant grown in Tibet. Moreover, the yield per plant had a significant positive correlation with the number of siliques per plant, branching number, and the number of seeds per silique (Table 2). SC3, SC10, SC29, and SC37 had greater plant height than others. In addition, SC3, SC25, and SC37 had more branches, and SC10, SC25, and SC37 had more siliques per plant. Material SC27 had the largest number of seeds per silique.

Fig. 5
figure 5

Different genotypes of Brassica napus were grown to maturity in the plateau environment (Lhasa, Tibet). A represents material SC10, B represents material SC25, C represents material SC32, and D represents material Zangyou12. Bars indicates 50 cm

Table 1 Comparison of differences in agronomic traits: plant height, number of branches, number of siliques per plant and number of seeds per silique in different genotypes of Brassica napus under plateau conditions in Lhasa
Table 2 Correlation analysis of agronomic traits, yield per plant and net photosynthetic rate (An) of seedling leaves of different genotypes of Brassica napus in the field

Differences in fatty acid content and composition

Fatty acids constitute the primary components of rapeseed oils, with oleic acid (C18H34O2), linoleic acid (C18H32O2) and erucic acid (C22H42O2) serving as quality indicators. In the plateau environment, the oleic acid content of B. napus varieties SC3, SC10, SC25, SC27 and SC37 ranged from 67.02% to 73.44%, while in the Chengdu Plain it ranged from 60.35% to 70.27%. Therefore, the oleic acid content of rapeseed increased in plateau (Additional file 1: Table S6). The linoleic acid content increased in SC27 and SC37 under plateau conditions, while SC3, SC10 and SC25 decreased. The erucic acid content of high erucic acid material SC32 was 37.57% in the plateau and 38.64% in the plain. (Fig. 6).

Fig. 6
figure 6

Fatty acid composition in seeds of different rapeseed varieties in two ecological environments: plain (Chengdu, Sichuan) and plateau (Lhasa, Tibet). AF represent the fatty acid composition of Brassica napus from materials SC3, SC10, SC25, SC27, SC37 and SC32, respectively

Photosynthetic carbon metabolism

Once the light intensity reaches the leaves’ saturation point, their photosynthetic rate no longer increases. At this stage, factors such as electron transfer reactions, Rubisco activity, phosphoenolpyruvate (PEP) metabolism become limiting factors. Rubisco, RuBPcase, SBPase, RCA, CA and PEPcase are all critical enzymes in the dark reactions of photosynthesis. In plateau conditions, the activities of Rubisco, CA, SBPase, and RCA in B. napus leaves were significantly lower than those in the plain. The carboxylation activity of Rubisco and PEPcase increased in plateau, but the differences were not significant. (Fig. 7A).

Fig. 7
figure 7

Enzyme activities (A, the left side of the heat map shows Lhasa, the right side shows Chengdu) and photosynthetic metabolite contents (B) related to photosynthetic carbon transfer in seedling leaves of two ecological environments of Brassica napus varieties: SC3, SC10, and SC25 in plain (Chengdu, Sichuan) and plateau (Lhasa, Tibet). Different letters indicate significant differences between different genotypes of rapeseed. (P < 0.05)

Changes in environmental factors can have an impact on carbon metabolism in leaves, resulting in changes in the carbohydrate content. In Lhasa, SC3, SC10 and SC25 showed a decrease in soluble sugar and starch content. Under the same environmental conditions, various rapeseed genotypes exhibited different leaf carbohydrate content, with material SC25 showing a higher concentration of photosynthetic products than SC3 and SC10. (Fig. 7B).

Discussion

Photosynthesis is the physiological basis for crop yield, and the strength of light energy utilization determines the crop yield [28]. The selection and development of rapeseed varieties with high photosynthetic efficiency to enhance light energy utilization are crucial for increasing production. When CO2 concentration is lower than two-thirds of the normal atmospheric CO2 concentration, it affects plant growth [29]. The experimental base of the Lhasa Academy of Agricultural and Animal Husbandry Sciences is seven times higher in altitude than the Chengdu Plain at the same latitude. It has thin air, intense photosynthetically active radiation, and an atmospheric CO2 concentration about two-thirds that of the Chengdu Plain.

Both light intensity and CO2 concentration affects the efficiency of light energy utilization in crops. This study showed that different genotypes of rapeseed seedlings respond differently to changes in light intensity and CO2 concentration. B. napus varieties SC3, SC10, SC25, SC27, and SC37, showed high photosynthetic efficiency when subjected to high light intensity (PAR of 1500 μmolm−2 s−1) and low CO2 concentration (300 μmol mol−1) conditions. In addition, these varieties exhibited significantly higher net photosynthesis rate (An), yield per plant, and biomass compared to others in plateau. Interestingly, SC6 and SC26 with high photosynthetic efficiency under high light intensity conditions (PAR of 1500 μmolm−2 s−1) were not dominant in the plateau phenotype. This indicates that low CO2 concentration is the key environmental factor limiting rapeseed growth in the plateau. On the plateau, the An of rapeseed leaves at the seedling stage are lower than the results observed under high light intensity (PAR of 1500 μmol m−2 s−1) and atmospheric CO2 concentration conditions in the plain. This also indicates that the low CO2 concentration limits the photosynthesis of rapeseed leaves when light intensity reaches saturation on the plateau. Therefore, increasing field CO2 concentration through agricultural production measures in plateau can enhance photosynthetic efficiency and increase rapeseed production.

There is a correlation between the photosynthetic rate and the morphological structure of plants. Biomass and agronomic traits are important indicators of crop growth. Studies have shown a significant positive correlation between soybean yield and leaf net photosynthetic rate [30], but some research shows that the photosynthetic rate of corn is unrelated to productivity, and selecting corn varieties with high photosynthetic rate may even lead to reduced productivity [31]. This study found that the high photosynthetic efficiency materials SC3, SC10, SC25, SC29 and SC37 in plateau environment had significantly higher yield per plant, biomass, and oil content compared to others. Correlation analysis also indicates a significant positive correlation between An and the yield per plant of rapeseed. Therefore, it shows that high photosynthetic efficiency rapeseed genotypes have a certain yield potential, consistent with previous studies [32]. Breeding rapeseed materials with high photosynthetic efficiency adapted to low CO2 concentration is crucial for improving rapeseed production and quality in plateau regions.

The carbon cycle of photosynthesis involves CO2 fixation, photosynthetic product allocation, and carbon metabolism, regulated by multiple enzymes, which significantly impact crop yield, growth, and adaptability. Under stress conditions, the activity of PEPcase increases in C3 plants [33]. The results of this study show that under plateau conditions, the activities of Rubisco, CA, SBPase and RCA are reduced in SC3, SC10 and SC25. This reduction may result from low CO2 concentration, limiting the rate of photosynthesis, causing insufficient energy and carbon supply and the activation of negative regulatory mechanisms. Due to the intense light and low CO2 concentration in the plateau environment, rapeseed leaves, upon reaching light saturation, undergo continuous carbon reactions, consuming ATP generated in the light reactions. Consequently, the carboxylation activity of Rubisco increases in the plateau environment. The low CO2 concentration can reduce the synthesis of photosynthetic products in plant leaves [34], which is consistent with the results of our study. Under plateau conditions, SC3, SC10, and SC25 have significantly lower soluble sugar and starch contents in their leaves compared to the Chengdu Plain. These differences may be related to the decreased photosynthesis rate of the plants. Therefore, exploring the key pathway of photosynthesis in rapeseed may help to elucidate the molecular mechanisms of C3 plant adaptation to plateau region (Fig. 8).

Fig. 8
figure 8

Mechanisms of changes in leaf photosynthesis at physiological and biochemical levels in rapeseed under plateau environment. The pattern diagrams (1) Rubisco activate (RCA), (2) carboxylation activity of Rubisco, (3) Sedoheptulose-1,7-bisphosphatase (SBPase), (4) Carbonic Anhydrase(CA) (5) Phosphoenolpyruvate carboxylase (PEPcase), and (6) represent photosynthetic product formation

Rapeseed is one of the important sources of vegetable oil, and its fatty acid composition directly impacts the quality and nutritional value of the oil. Previous research has found that light intensity affects seed oil content and fatty acid synthesis. In this study, we found that under plateau conditions, the oleic acid content increased, and the erucic acid content of high-erucic acid rapeseed decreased. High light intensity provided a large amount of ATP and NADPH for fatty acid synthesis in plastids, favoring oleic acid synthesis [35]. This could be due to the low atmospheric CO2 concentration, which affects the carbon metabolism of rapeseed, leading to changes in fatty acid metabolism and synthesis. This offers a new perspective for the breeding and design of industrial rapeseed.

Conclusion

During the cultivation period of rapeseed on the plateau (Lhasa, Tibet), sunlight intensity is approximately double that of the plain (Chengdu, Sichuan), and atmospheric CO2 concentration is about two-thirds of that in the plain. The rapeseed materials SC3, SC10, SC25, SC27, SC29 and SC37 with high photosynthetic efficiency under low CO2 concentrations rather than high light intensity, exhibited significant advantages in biomass, yield, and oil content when cultivated on the plateau, indicating that the CO2 is the key environmental factor which limited rapeseed production in plateau. Simultaneously, PEPcase activity in rapeseed leaves increased at plateau, while SBPase and RCA activities decreased, and soluble sugar and starch contents also decreased. The oleic acid content in rapeseed increased, while the erucic acid content exhibited a decreasing trend. In conclusion, we found that both the key enzyme activities of carbon reactions and carbon metabolism levels in rapeseed are reduced in plateau environment. The key environmental factor limiting plateau rapeseed production is the low atmospheric CO2 concentration. Also, the rapeseed materials SC3, SC10, SC25, SC27, SC29, and SC37 exhibit the higher adaptabilities and breeding values in plateau environments. Hence, our study provides the theoretical and practical foundations for plateau-adapted rapeseed breeding.

Materials and methods

Plant material and growth conditions

40 Brassica napus varieties (designated as SC1–40) were used as experimental materials. Seeds that were plump and uniform in size were selected and treated with 10% H2O2 for 30 min for surface sterilization. After wash with sterile water for 2–3 times, the seeds were placed on two layers of moistened filter paper in Petri dishes for germination under a 14-h light/10-h dark photoperiod at 28 °C in the growth chamber. After seed germination, they were transplanted into pots (14 cm × 13 cm) filled with nutrient soil, with 2 seedlings per pot, and were cultivated in the plant culture room (located at 104°06′E, 30°67′N, and 500 m above sea level). Field experiments were conducted at the experimental base of the Tibet Lhasa Academy of Agricultural and Animal Husbandry Sciences, located at coordinates (91°06′E, 29°36′N), at an altitude of 3650 m above sea level. The experimental plots were arranged in a completely randomized block design with three replications of the plots, with each plot measuring 1.8 m2 (6 × 0.3 m), consisting of 6 rows with a row spacing of 0.3 m and a plant spacing of 0.16 m. Standard field management practices were followed uniformly.

Photosynthetic leaf gas exchange measurements

Photosynthetic parameters of B. napus at the six-leaf stage were assessed using a portable photosynthesis measurement instrument, Li-6400XT (Li-Cor, Lincoln, NE, USA), with a leaf chamber size of 2 × 3 cm2. The red–blue light source, 6400-02B, was employed, with a leaf chamber temperature set at 28 °C. Measurements were conducted under the following conditions: (1) the leaf chamber light intensity was set at 1500 μmol m−2 s−1, and the chamber’s CO2 concentration at the ambient atmospheric CO2 concentration. (2) The leaf chamber light intensity was set at 1500 μmol m−2 s−1, and the CO2 concentration in the chamber was adjusted to 300 μmol mol−1. (3) The leaf chamber light intensity was set at 1000 μmol m−2 s−1, and the chamber’s CO2 concentration was set at 300 μmol mol−1. Under given conditions, photosynthetic parameters of the sixth leaf of 40 rapeseed materials were measured, including net photosynthesis rate (An; μmol m−2 s−1), intercellular CO2 concentration (Ci; μmol mol−1), transpiration rate (Tr; mmol m−2 s−1), and stomatal conductance (Gs; mmol m−2 s−1). This study measured the photosynthetic characteristics of B. napus leaves in the plateau region of Tibet. Random selection of five plants with similar growth from each experimental plot was conducted. The temperature inside the leaf chamber was maintained at a constant 28 °C, while the light intensity and CO2 concentration were consistent with the natural environmental conditions outside.

Plant growth and yields

Five plants per plot were randomly selected at the maturity stage of B. napus, and biomass, field agronomic traits and seed oil content were measured. Field agronomic traits indicators comprised plant height, number of branches, number of effective siliques per plant, number of seeds per silique and yield per plant.

Leaf carbon metabolism physiological indicators

The enzyme activities of the key enzymes involved in photosynthetic carbon reactions, namely, RuBPcase, PEPCase, RCA and SBPase, were measured. Samples of fresh leaf tissue(0.1 g)were extracted using a tissue homogenizer with 900 μL phosphate buffer (pH = 7.2–7.4, concentration of 0.01 mol/L) at 4 ℃ The resulting sample solution was diluted fivefold with sample diluent and added into the enzyme plate for an incubation at 37 ℃ for 30 min followed by 5 times washing with detergent. Then, except for the blank wells, each well was supplemented with enzyme reagent for incubation at 37 ℃ for 30 min, followed by 5 washes at the end of the reaction. Subsequently, chromogenic reagent was added to the plate and allowed to develop color at 37 ℃ for 10 min. The reaction was then terminated using the termination solution. Finally, the absorbance value was determined by setting the wavelength at 450 nm using a Microplate Reader, and the zero of the blank wells was adjusted accordingly.

The soluble sugar and starch contents were determined by anthrone colourimetry. Oil content and fatty acid content of rapeseed were determined using a standard benchtop NIR spectrometer (DS 2500, Foss).

Statistical analysis

The data were statistically analyzed using SPSS 21.0 (SPSS Inc., Chicago, IL, USA), and Origin 9.0 (OriginLab Corporation, Northampton, MA, USA) was used for graphical presentation of data. Pattern drawing by Figdraw website.

Availability of data and materials

Data for the results of this study are available from the paper and its Additional Information files.

References

  1. Abbadi A, Leckband G. Rapeseed breeding for oil content, quality, and sustainability. Eur J Lipid Sci Technol. 2011;113(10):1198–206. https://doi.org/10.1002/ejlt.201100063.

    Article  CAS  Google Scholar 

  2. Xiong HY, et al. Transcriptomic analysis of rapeseed (Brassica napus L.) seed development in Xiangride, Qinghai Plateau, reveals how its special eco-environment results in high yield in high-altitude areas. Front Plant Sci. 2022;13:16. https://doi.org/10.3389/fpls.2022.927418.

    Article  Google Scholar 

  3. Heyneke E, Fernie AR. Metabolic regulation of photosynthesis. Biochem Soc Trans. 2018;46:321–8. https://doi.org/10.1042/BST20170296.

    Article  CAS  PubMed  Google Scholar 

  4. Sun JD, et al. FACE-ing the global change: opportunities for improvement in photosynthetic radiation use efficiency and crop yield. Plant Sci. 2009;177(6):511–22. https://doi.org/10.1016/j.plantsci.2009.08.003.10.1111/tpj.14568.

    Article  CAS  Google Scholar 

  5. Faralli M, Lawson T. Natural genetic variation in photosynthesis: an untapped resource to increase crop yield potential? Plant J. 2020;101(3):518–28. https://doi.org/10.1111/tpj.14568.

    Article  CAS  PubMed  Google Scholar 

  6. Kromdijk J, et al. Improving photosynthesis and crop productivity by accelerating recovery from photoprotection. Science. 2016;354(6314):857–61. https://doi.org/10.1126/science.aai8878.

    Article  ADS  CAS  PubMed  Google Scholar 

  7. Jiang GM, et al. Changes in the rate of photosynthesis accompanying the yield increase in wheat cultivars released in the past 50 years. J Plant Res. 2003;116(5):347–54. https://doi.org/10.1007/s10265-003-0115-5.

    Article  CAS  PubMed  Google Scholar 

  8. Mohammed AR, Tarpley L. Effects of high night temperature and spikelet position on yield-related parameters of rice (Oryza sativa L.) plants. Eur J Agron. 2010;33(2):117–23. https://doi.org/10.1111/j.1439-037X.2010.00439.x.

    Article  CAS  Google Scholar 

  9. Chen JW, et al. Biomass accumulation and partitioning, photosynthesis, and photosynthetic induction in field-grown maize (Zea mays L.) under low- and high-nitrogen conditions. Acta Physiol Plant. 2013;35(1):95–105. https://doi.org/10.1007/s11738-012-1051-6.

    Article  MathSciNet  CAS  Google Scholar 

  10. Liu E, et al. Transcriptomic analysis reveals mechanisms for the different drought tolerance of sweet potatoes. Front Plant Sci. 2023;14:1136709. https://doi.org/10.3389/fpls.2023.1136709.

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  11. Ju X, Li Z. Study of different types of rape (Brassica napus L.) cultivars (lines) relationship between photosynthetic physiological indices and yield. J Anhui Agri Sci. 2012;40(22):11213–5. https://doi.org/10.13989/j.cnki.0517-6611.2012.22.106.

    Article  Google Scholar 

  12. Jumrani K, Bhatia VS. Influence of different light intensities on specific leaf weight, stomatal density photosynthesis and seed yield in soybean. Plant Physiol Rep. 2020;25(2):277–83. https://doi.org/10.1007/s40502-020-00508-6.

    Article  CAS  Google Scholar 

  13. Panda D, et al. Impact of low light stress on physiological, biochemical and agronomic attributes of rice. J Pharmacogn Phytochem. 2019;8(1):1814–21.

    CAS  Google Scholar 

  14. Xin P, et al. Optimization and control of the light environment for greenhouse crop production. Comput Electron Agric. 2019;9(1):8650. https://doi.org/10.1016/j.compag.2020.105854.

    Article  Google Scholar 

  15. Usuda H. Effects of elevated CO2 on the capacity for photosynthesis of a single leaf and a whole plant, and on growth in a radish. Plant Cell Physiol. 2006;47(2):262–9. https://doi.org/10.1093/pcp/pci244.

    Article  CAS  PubMed  Google Scholar 

  16. Chen X, et al. Effect of elevated CO2 concentration on photosynthesis and antioxidative enzyme activities of wheat plant grown under drought condition. J Appl Ecol. 2000;11(6):881–4. https://doi.org/10.13287/j.1001-9332.2000.0210.

    Article  CAS  Google Scholar 

  17. von Caemmerer S. Rubisco carboxylase/oxygenase: from the enzyme to the globe: a gas exchange perspective. J Plant Physiol. 2020;252:9. https://doi.org/10.1016/j.jplph.2020.153240.

    Article  CAS  Google Scholar 

  18. Qu YC, et al. Overexpression of both Rubisco and Rubisco activase rescues rice photosynthesis and biomass under heat stress. Plant Cell Environ. 2021;44(7):2308–20. https://doi.org/10.1111/pce.14051.

    Article  CAS  PubMed  Google Scholar 

  19. Ding F, Wang ML, Zhang SX. Overexpression of a Calvin cycle enzyme SBPase improves tolerance to chilling-induced oxidative stress in tomato plants. Sci Hortic. 2017;214:27–33. https://doi.org/10.1016/j.scienta.2016.11.010.

    Article  CAS  Google Scholar 

  20. Suzuki Y, et al. Effects of co-overproduction of sedoheptulose-1,7-bisphosphatase and Rubisco on photosynthesis in rice. Soil Sci Plant Nutr. 2019;65(1):36–40. https://doi.org/10.1080/00380768.2018.1530053.

    Article  CAS  Google Scholar 

  21. Ignatova L, et al. Carbonic anhydrases in photosynthesizing cells of C3 higher plants. Metabolites. 2019. https://doi.org/10.3390/metabo9040073.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Sage RF. The evolution of C4 photosynthesis. New Phytol. 2004;161(2):341–70. https://doi.org/10.1111/j.1469-8137.2004.00974.x.

    Article  CAS  PubMed  Google Scholar 

  23. Hussain S, et al. Photosynthesis research under climate change. Photosynth Res. 2021;150(1–3):5–19. https://doi.org/10.1007/s11120-021-00861-z.

    Article  CAS  PubMed  Google Scholar 

  24. Kuai J, et al. Response of leaf carbon metabolism and dry matter accumulation to density and row spacing in two rapeseed(Brassica napus L.) genotypes with differing plant architectures. Crop J. 2022;10(3):680–91. https://doi.org/10.1016/j.cj.2021.10.006.

    Article  Google Scholar 

  25. Liu JH, et al. Climate suitability assessment on the Qinghai-Tibet Plateau. Sci Total Environ. 2022;816:14. https://doi.org/10.1016/j.scitotenv.2021.151653.

    Article  CAS  Google Scholar 

  26. Gelsor N, et al. Ground-based measurements of global solar radiation and UV radiation in Tibet. Spectr Spectr Anal. 2019;39(6):1683–8. https://doi.org/10.3964/j.issn.1000-0593(2019)06-1683-06.

    Article  CAS  Google Scholar 

  27. Schleussner C-F, et al. Differential climate impacts for policy-relevant limits to global warming: the case of 1.5℃ and 2℃. Earth Syst Dynam. 2016;7(2):327–51. https://doi.org/10.5194/esd-7-327-2016.

    Article  ADS  Google Scholar 

  28. Li RQ, et al. Research progress in improving photosynthetic efficiency. Int J Mol Sci. 2023;24(11):13. https://doi.org/10.3390/ijms24119286.

    Article  ADS  CAS  Google Scholar 

  29. Gerhart LM, Ward JK. Plant responses to low CO2 of the past. New Phytol. 2010;188(3):674–95. https://doi.org/10.1111/j.1469-8137.2010.03441.x.

    Article  PubMed  Google Scholar 

  30. Hay WT, et al. Enhancing soybean photosynthetic CO2 assimilation using a cyanobacterial membrane protein, ictB. J Plant Physiol. 2017;212:58–68. https://doi.org/10.1016/j.jplph.2017.02.003.

    Article  CAS  PubMed  Google Scholar 

  31. Hanson WD. Selection for differential productivity among juvenile maize plants- associated net photosynthetic rate and leaf area changes. Crop Sci. 1971;11(3):334–9. https://doi.org/10.2135/cropsci1971.0011183X001100030007x.

    Article  Google Scholar 

  32. Biabani A, et al. Physiological traits, yield, and yield components relationship in winter and spring canola. J Sci Food Agric. 2021;101(8):3518–28. https://doi.org/10.1002/jsfa.11094.

    Article  CAS  PubMed  Google Scholar 

  33. Chen S, et al. Encoded C4 homologue enzymes genes function under abiotic stresses in C3 plant. Plant Signal Behav. 2022;17(1):2115634. https://doi.org/10.1080/15592324.2022.2115634.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Liu L, et al. Multi-scale modeling of Arabidopsis thaliana response to different CO2 conditions: from gene expression to metabolic flux. J Integr Plant Biol. 2016;58(1):2–11. https://doi.org/10.1111/jipb.12370.

    Article  CAS  PubMed  Google Scholar 

  35. Wu XL, et al. BnWRI1 coordinates fatty acid biosynthesis and photosynthesis pathways during oil accumulation in rapeseed. J Integr Plant Biol. 2014;56(6):582–93. https://doi.org/10.1111/jipb.12158.

    Article  CAS  PubMed  Google Scholar 

Download references

Funding

This research was supported by the National Natural Science Foundation of China (32272167 and 32341028), the National Key Research and Development Program of China (2022YFD1601502-2 and 2023YFD1200202) and the Fundamental Research Funds for the Central Universities (SCU2019D013).

Author information

Authors and Affiliations

Authors

Contributions

Conceptualization, YZ and RW; funding acquisition, YZ and RW; investigation, SL, LT and JF; data analysis, SL, CZ, YZ and MY; writing original draft, SL and RW; reviewing and editing, YZ, LT and MW.

Corresponding authors

Correspondence to Rui Wang or Yun Zhao.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1

: Table S1. Photosynthetic parameters of rapeseed varieties at 1500 μmol m−2s−1 photosynthetically active radiation and 300 μmol mol1 CO2 concentration. Table S2. Photosynthetic parameters of rapeseed varieties at 1000 μmol m−2s−1 photosynthetically active radiation and 300 μmol mol1 CO2 concentration. Table S3. Photosynthetic parameters of rapeseed varieties at 1500 μmol m−2s−1 photosynthetically active radiation. Table S4. Photosynthetic parameters among rapeseed varieties in a plateau environment. An net photosynthetic rate, Gs stomatal conductance, Ci intercellular carbon dioxide concentration, Tr transpiration rate. Table S5. Oil content and yield in seeds of different rapeseed varieties in two ecological environments: plain (Chengdu, Sichuan) and plateau (Lhasa, Tibet). Table S6. Fatty acid composition in seeds of different rapeseed varieties in two ecological environments: plain (Chengdu, Sichuan) and plateau (Lhasa, Tibet).

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Liu, S., Tang, L., Fu, J. et al. Low CO2 concentration, a key environmental factor for developing plateau adapted rapeseed. Biotechnol Biofuels 17, 28 (2024). https://doi.org/10.1186/s13068-024-02481-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13068-024-02481-w

Keywords