Evan A Perkowski, Ezinwanne Ezekannagha, Nicholas G Smith
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Instead, elevated CO2 decreased the maximum rate of ribulose-1,5-bisophosphate oxygenase/carboxylase (Rubisco) carboxylation more strongly than it decreased the maximum rate of electron transport for ribulose-1,5-bisphosphate (RuBP) regeneration, increasing net photosynthesis by allowing rate-limiting steps to approach optimal coordination. Increasing fertilization enhanced positive whole-plant responses to elevated CO2 due to increased below-ground carbon allocation and nitrogen uptake. Inoculation with nitrogen-fixing bacteria did not influence plant responses to elevated CO2. 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引用次数: 0
摘要
植物通过降低叶片氮含量和光合能力来应对大气中二氧化碳浓度的增加,这种模式与净光合作用和生长的增加相对应。尽管长期以来人们认为氮的可用性调节了这些反应,但生态进化最优理论认为,叶片对二氧化碳升高的反应是由叶片对构建和维持光合酶的氮需求驱动的,与氮的可用性无关。本研究研究了2种CO2、2种接种和9种氮肥处理对甘氨酸(Glycine max L., Merr)叶片和全株的响应。施氮和接种没有改变叶片对CO2升高的光合响应。相反,升高的CO2降低Rubisco羧化的最大速率比降低RuBP再生的最大电子传递速率更强烈,通过允许限速步骤接近最佳协调来增加净光合作用。由于增加了地下碳分配和氮吸收,增加施肥增强了整个植物对二氧化碳升高的积极响应。接种固氮菌不影响植物对CO2升高的响应。这些结果证实了氮有效性在植物对CO2升高的响应中的作用,表明叶片光合响应受叶片氮需求的调节,而整个植物的响应受氮有效性的限制。
Nitrogen demand, availability, and acquisition strategy control plant responses to elevated CO2.
Plants respond to increasing atmospheric CO2 concentrations by reducing leaf nitrogen content and photosynthetic capacity-patterns that correspond with increased net photosynthesis and growth. Despite the longstanding notion that nitrogen availability regulates these responses, eco-evolutionary optimality theory posits that leaf-level responses to elevated CO2 are driven by leaf nitrogen demand for building and maintaining photosynthetic enzymes and are independent of nitrogen availability. In this study, we examined leaf and whole-plant responses of Glycine max L. (Merr) subjected to full-factorial combinations of two CO2, two inoculation, and nine nitrogen fertilization treatments. Nitrogen fertilization and inoculation did not alter leaf photosynthetic responses to elevated CO2. Instead, elevated CO2 decreased the maximum rate of ribulose-1,5-bisophosphate oxygenase/carboxylase (Rubisco) carboxylation more strongly than it decreased the maximum rate of electron transport for ribulose-1,5-bisphosphate (RuBP) regeneration, increasing net photosynthesis by allowing rate-limiting steps to approach optimal coordination. Increasing fertilization enhanced positive whole-plant responses to elevated CO2 due to increased below-ground carbon allocation and nitrogen uptake. Inoculation with nitrogen-fixing bacteria did not influence plant responses to elevated CO2. These results reconcile the role of nitrogen availability in plant responses to elevated CO2, showing that leaf photosynthetic responses are regulated by leaf nitrogen demand while whole-plant responses are constrained by nitrogen availability.
期刊介绍:
The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology.
Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.