{"title":"高浓度co2对工业甘薯品种CX-1生长的影响","authors":"G. Runion, S. Prior, T. Monday, J. Ryan-Bohac","doi":"10.2525/ECB.56.89","DOIUrl":null,"url":null,"abstract":"Atmospheric CO2 concentrations have been steadily rising each year, from approximately 315 ppm in 1958 to 385 ppm in 2009 (Keeling et al., 2009), and are continuing to rise, with some estimates showing an increase to 700 ppm by the end of this century (Meehl et al., 2007). Generally, increases in CO2 are largely attributed to anthropogenic causes, including fossil fuel combustion and land use changes such as deforestation and urbanization (Hegerl et al., 2007). It is well established that elevated CO2 increases growth and yield of most plant species (Kimball, 1983). This added growth and yield is primarily attributed to increased rates of photosynthesis and water use efficiency (Rogers and Dahlman, 1993; Amthor, 1995). Growth in elevated CO2 induces a partial closure of leaf stomatal guard cells resulting in reduced transpiration and water loss (Jones and Mansfield, 1970) which increases water use efficiency for plants with both C3 and C4 photosynthetic pathways (Prior et al., 2011). However, research has shown that biomass response to atmospheric CO2 enrichment is generally greater for plants with a C3 (33 40% increase) vs. a C4 (10 15% increase) photosynthetic pathway (Kimball, 1983; Poorter, 1993; Prior et al., 2003; 2005). Plants with a C3 photosynthetic pathway show both increased water use efficiency and increased photosynthesis, while the CO2concentrating mechanism used by C4 plants limits their photosynthetic response to CO2 enrichment (Amthor and Loomis, 1996). Sweetpotatoes [Ipomoea batatas (L.) Lam.] have a C3 photosynthetic pathway and, like most plants, have a positive growth response to elevated CO2 (Bhattacharya et al., 1985; Biswas et al., 1996). In fact, total storage root dry weight response to CO2 enrichment can exceed the general range for C3 plants. Bhattacharya et al. (1985) reported increases of 87% at 675 mol mol 1 and 172.6% at 1,000 mol mol 1 for dry weight of ‘Georgia Jet’ storage roots. Biswas et al. (1996) reported total storage root dry weight increases of 44% and 75% at 665 mol mol 1 for two growing seasons. These large increases are not surprising since it is known that plants with a strong sink for photosynthate, such as sweetpotato storage roots, can respond to a greater degree than plants with other growth habits (Idso et al., 1988). In addition to use as a food crop, sweetpotato storage roots have been shown to be a good source material for bioethanol production (Qiu et al., 2010). In fact, Ziska et al. (2009) reported that sweetpotatoes (cv. Beauregard) have the ability to out-produce other sources of crop plant bioethanol (e.g., corn, potatoes, sugar cane, and sugar beets) in both Maryland and Alabama. Recently, several “industrial cultivars” of sweetpotatoes have been bred specifically for bioethanol production. For example, storage roots of the industrial sweetpotato cultivar CX-1 (Ryan-","PeriodicalId":11762,"journal":{"name":"Environmental Control in Biology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Effects of Elevated CO 2 on Growth of the Industrial Sweetpotato Cultivar CX-1\",\"authors\":\"G. Runion, S. Prior, T. Monday, J. Ryan-Bohac\",\"doi\":\"10.2525/ECB.56.89\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Atmospheric CO2 concentrations have been steadily rising each year, from approximately 315 ppm in 1958 to 385 ppm in 2009 (Keeling et al., 2009), and are continuing to rise, with some estimates showing an increase to 700 ppm by the end of this century (Meehl et al., 2007). Generally, increases in CO2 are largely attributed to anthropogenic causes, including fossil fuel combustion and land use changes such as deforestation and urbanization (Hegerl et al., 2007). It is well established that elevated CO2 increases growth and yield of most plant species (Kimball, 1983). This added growth and yield is primarily attributed to increased rates of photosynthesis and water use efficiency (Rogers and Dahlman, 1993; Amthor, 1995). Growth in elevated CO2 induces a partial closure of leaf stomatal guard cells resulting in reduced transpiration and water loss (Jones and Mansfield, 1970) which increases water use efficiency for plants with both C3 and C4 photosynthetic pathways (Prior et al., 2011). However, research has shown that biomass response to atmospheric CO2 enrichment is generally greater for plants with a C3 (33 40% increase) vs. a C4 (10 15% increase) photosynthetic pathway (Kimball, 1983; Poorter, 1993; Prior et al., 2003; 2005). Plants with a C3 photosynthetic pathway show both increased water use efficiency and increased photosynthesis, while the CO2concentrating mechanism used by C4 plants limits their photosynthetic response to CO2 enrichment (Amthor and Loomis, 1996). Sweetpotatoes [Ipomoea batatas (L.) Lam.] have a C3 photosynthetic pathway and, like most plants, have a positive growth response to elevated CO2 (Bhattacharya et al., 1985; Biswas et al., 1996). In fact, total storage root dry weight response to CO2 enrichment can exceed the general range for C3 plants. Bhattacharya et al. (1985) reported increases of 87% at 675 mol mol 1 and 172.6% at 1,000 mol mol 1 for dry weight of ‘Georgia Jet’ storage roots. Biswas et al. (1996) reported total storage root dry weight increases of 44% and 75% at 665 mol mol 1 for two growing seasons. These large increases are not surprising since it is known that plants with a strong sink for photosynthate, such as sweetpotato storage roots, can respond to a greater degree than plants with other growth habits (Idso et al., 1988). In addition to use as a food crop, sweetpotato storage roots have been shown to be a good source material for bioethanol production (Qiu et al., 2010). In fact, Ziska et al. (2009) reported that sweetpotatoes (cv. Beauregard) have the ability to out-produce other sources of crop plant bioethanol (e.g., corn, potatoes, sugar cane, and sugar beets) in both Maryland and Alabama. Recently, several “industrial cultivars” of sweetpotatoes have been bred specifically for bioethanol production. 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引用次数: 4
摘要
大气中的二氧化碳浓度每年都在稳步上升,从1958年的大约315 ppm上升到2009年的385 ppm (Keeling等人,2009年),并且还在继续上升,一些估计显示到本世纪末将增加到700 ppm (Meehl等人,2007年)。一般来说,二氧化碳的增加主要归因于人为原因,包括化石燃料燃烧和土地利用变化,如森林砍伐和城市化(Hegerl et al., 2007)。众所周知,二氧化碳浓度升高会促进大多数植物物种的生长和产量(Kimball, 1983)。这种增加的生长和产量主要归因于光合作用和水分利用效率的提高(Rogers和Dahlman, 1993;Amthor, 1995)。在高CO2环境下的生长诱导叶片气孔保护细胞部分关闭,导致蒸腾作用和水分损失减少(Jones和Mansfield, 1970),从而提高了具有C3和C4光合途径的植物的水分利用效率(Prior等,2011)。然而,研究表明,对于C3(增加33.40%)光合途径的植物,生物量对大气CO2富集的响应通常大于C4(增加10.15%)光合途径的植物(Kimball, 1983;要隘,1993;Prior et al., 2003;2005)。C3光合途径的植物既提高了水分利用效率,也增加了光合作用,而C4植物使用的CO2浓缩机制限制了它们对CO2富集的光合反应(Amthor和Loomis, 1996)。红薯(L.)林。]有C3光合途径,并且像大多数植物一样,对升高的CO2有积极的生长反应(Bhattacharya et al., 1985;Biswas et al., 1996)。事实上,总库存量根干重对CO2富集的响应可以超过C3植物的一般范围。Bhattacharya等人(1985)报道,在675 mol mol 1条件下,“Georgia Jet”储存根的干重增加了87%,在1000 mol mol 1条件下增加了172.6%。Biswas et al.(1996)报道,在665 mol mol / 1条件下,两个生长季节总储藏根干重分别增加44%和75%。这些大幅增加并不令人惊讶,因为众所周知,具有强大光合作用库的植物,如甘薯储存根,可以比具有其他生长习惯的植物做出更大程度的响应(Idso等人,1988)。除了用作粮食作物外,甘薯储藏根已被证明是生产生物乙醇的良好原料(Qiu et al., 2010)。事实上,Ziska et al.(2009)报道甘薯(cv。在马里兰州和阿拉巴马州,博雷加德(Beauregard)有能力生产出比其他农作物(如玉米、土豆、甘蔗和甜菜)更多的生物乙醇。最近,一些专门用于生物乙醇生产的甘薯“工业品种”被培育出来。例如,工业红薯品种CX-1 (Ryan- 1)的储存根
Effects of Elevated CO 2 on Growth of the Industrial Sweetpotato Cultivar CX-1
Atmospheric CO2 concentrations have been steadily rising each year, from approximately 315 ppm in 1958 to 385 ppm in 2009 (Keeling et al., 2009), and are continuing to rise, with some estimates showing an increase to 700 ppm by the end of this century (Meehl et al., 2007). Generally, increases in CO2 are largely attributed to anthropogenic causes, including fossil fuel combustion and land use changes such as deforestation and urbanization (Hegerl et al., 2007). It is well established that elevated CO2 increases growth and yield of most plant species (Kimball, 1983). This added growth and yield is primarily attributed to increased rates of photosynthesis and water use efficiency (Rogers and Dahlman, 1993; Amthor, 1995). Growth in elevated CO2 induces a partial closure of leaf stomatal guard cells resulting in reduced transpiration and water loss (Jones and Mansfield, 1970) which increases water use efficiency for plants with both C3 and C4 photosynthetic pathways (Prior et al., 2011). However, research has shown that biomass response to atmospheric CO2 enrichment is generally greater for plants with a C3 (33 40% increase) vs. a C4 (10 15% increase) photosynthetic pathway (Kimball, 1983; Poorter, 1993; Prior et al., 2003; 2005). Plants with a C3 photosynthetic pathway show both increased water use efficiency and increased photosynthesis, while the CO2concentrating mechanism used by C4 plants limits their photosynthetic response to CO2 enrichment (Amthor and Loomis, 1996). Sweetpotatoes [Ipomoea batatas (L.) Lam.] have a C3 photosynthetic pathway and, like most plants, have a positive growth response to elevated CO2 (Bhattacharya et al., 1985; Biswas et al., 1996). In fact, total storage root dry weight response to CO2 enrichment can exceed the general range for C3 plants. Bhattacharya et al. (1985) reported increases of 87% at 675 mol mol 1 and 172.6% at 1,000 mol mol 1 for dry weight of ‘Georgia Jet’ storage roots. Biswas et al. (1996) reported total storage root dry weight increases of 44% and 75% at 665 mol mol 1 for two growing seasons. These large increases are not surprising since it is known that plants with a strong sink for photosynthate, such as sweetpotato storage roots, can respond to a greater degree than plants with other growth habits (Idso et al., 1988). In addition to use as a food crop, sweetpotato storage roots have been shown to be a good source material for bioethanol production (Qiu et al., 2010). In fact, Ziska et al. (2009) reported that sweetpotatoes (cv. Beauregard) have the ability to out-produce other sources of crop plant bioethanol (e.g., corn, potatoes, sugar cane, and sugar beets) in both Maryland and Alabama. Recently, several “industrial cultivars” of sweetpotatoes have been bred specifically for bioethanol production. For example, storage roots of the industrial sweetpotato cultivar CX-1 (Ryan-