芋Colocasia esculenta (L.) Schott.
芋Colocasia esculenta (L.) Schott.
2. 芋(名医别录) 芋头(各地),水芋(广东海南),芋岌、毛艿(指小块茎)、毛芋(福建 福州),青皮叶、接骨草、独皮叶(云南南部),土芝、莒(古称),蹲鸱(史记)
Colocasia esculenta (L). Schott, Melet. 1: 18. 1832; Kunth, Enum. Pl. 3: 37. 1841; N. E. Brown in Journ. Linn. Soc. Bot. 36: 183. 1903; 广州植物志: 639. 1956; S. Y. Hu in Dansk Bot. Arkiv 23 (4) : 428. 1968; 秦岭植物志1 (1) : 278. 1976. ——rum esculentum L., Sp. Pl. ed. 1: 965. 1753, ed. 2: 1369. 1763. Arum chinense L. in Amoen. Acad. 4: 234. 1754. ——Arum peltatum βLam. Encycl. 3: 13. 1789. ——Caladium esculentum vent., Hort. Cels. 30. 1800; Willd. , Spec. 4: 489. 1805.——Colocasia antiquorum var. esculenta (L.) Schott, Syn. Ar. 42. 1859; Engl. in DC., Monogr. Phan. 2: 492. 1879; Krause in Engl., Pflanzenr. 71 (4, 23E): 67. 1920. ——Caladium colocasia (L.) W. F. Wight ex Safford in Contr. u. s. Nat. Herb. 9: 206. 1905.
湿生草本。块茎通常卵形,常生多数小球茎,均富含淀粉。叶2-3枚或更多。叶柄长于叶片,长20-90厘米,绿色,叶片卵状,长20-50厘米,先端短尖或短渐尖,侧脉4对,斜伸达叶缘,后裂片浑圆,合生长度达1/2-1/3,弯缺较钝,深3-5厘米,基脉相交成30度角,外侧脉2-3,内侧1-2条,不显。花序柄常单生,短于叶柄。佛焰苞长短不一,一般为20厘米左右:管部绿色,长约4厘米,粗2.2厘米,长卵形;檐部披针形或椭圆形,长约17厘米,展开成舟状,边缘内卷,淡黄色至绿白色。肉穗花序长约10厘米,短于佛焰苞:雌花序长圆锥状,长3-3.5厘米,下部粗1.2厘米;中性花序长约3-3.3厘米,细圆柱状;雄花序圆柱形,长4-4.5厘米,粗7毫米,顶端骤狭;附属器钻形,长约1厘米,粗不及1毫米。花期2-4月(云南)至8-9月(秦岭)。
原产我国和印度、马来半岛等地热带地方。我国南北长期以来进行栽培。埃及、菲律宾、印度尼西亚爪哇等热带地区也盛行栽种,视为主要食料。由于芋最喜高温湿润,栽培习惯愈向南也就愈盛。
块茎可食:可作羹菜,也可代粮或制淀粉,自古视为重要的粮食补助或救荒作物,台湾省雅美族至今以芋为主粮。叶柄可剥皮煮食或晒干贮用。全株为常用的猪饲料。块茎入药可治乳腺炎、口疮、痈肿疗疮、颈淋巴结核、烧烫伤、外伤出血,叶可治荨麻疹、疮疥。▽本种很少开花,通常用子芋繁殖。
我国的芋,早在《史记》中即有记载:“岷山之下,野有蹲鸱,至死不饥,注云芋也。盖芋魁之状若鸱之蹲坐故也”。经劳动人民长期因地制宜地选种培育,已有多种不伺类型的品种,其中常见的为下列3类:▽1. 多头芋:母芋分蘖群生,子芋甚少,台湾山地栽培的狗蹄芋;广西宜山的狗爪芋皆属此类。特征:植株矮,一株生多数叶丛,其下生多数母芋,结合成一块;粉质,味如栗子。▽2. 大魁芋:母芋单一或少数,肥大而味美,生子芋少,植株高大,分蘖力强,子芋少,但母芋甚发达,粉质,味美,产量高。如台湾、福建、广东等热带地区常见的槟榔心、竹节芋、红槟榔心、槟榔芋、面芋、红芋、黄芋、糯米芋、火芋等。▽3. 多子芋:子芋多而群生,母芋多纤维,味不美。本类分蘖力强,子芋为尾端细瘦的纺锤形,易自母芋分离,栽培目的是采收子芋。我国中部及北部栽培者多属此类。如台湾的早生白芋,浙江杭州的白梗芋,浙江慈溪的黄粉芋等。浙江的红顶芋、乌脚芋、台湾的乌柿芋等品种具红色或紫色叶柄,也属此类。
《Flora of China》 Vol. 23 (2010)
Colocasia esculenta (Linnaeus) Schott in Schott & Endlicher Melet. Bot. 18. 1832.
芋 yu
Arum esculentum Linnaeus, Sp. Pl. 2: 965. 1753; A. colocasia Linnaeus; Caladium colocasia (Linnaeus) W. Wight; C. esculentum (Linnaeus) Ventenat; Calla gaby Blanco; Colocasia antiquorum Schott var. esculenta (Linnaeus) Schott ex Seemann; C. formosana Hayata; C. konishii Hayata; C. neocaledonica Van Houtte.
Rhizome vertical to horizontal, tuberous, 3-5 cm or more (up to 15 cm) in diam. Stolons long or absent. Leaves 2 or 3 or more; petiole green, 25-80 cm, sheathing for 1/3-2/3 length; leaf blade adaxially matte waxy-glaucous and water-shedding (water sometimes forming "mercury droplets"), oblong-ovate to suborbicular, 13-45 × 10-35 cm, base shallowly cordate (sinus 1-4 cm), apex broadly and shortly cuspidate. Peduncle usually solitary, 16-26 cm. Spathe tube green, 3.5-5 × 1.2-1.5 cm; limb open proximally, cream-colored to golden yellow, lanceolate or elliptic, 10-19 × 2-5 cm, apex acuminate. Spadix: female zone conic, 3-3.5 × ca. 1.2 cm; ovary 1-3 mm in diam.; stigma subsessile, narrower than apex of ovary; sterile zone narrowly cylindric, 3-3.3 cm; sterile flowers (pistils) seen from above elongate, ca. 0.5 mm in diam.; male zone cylindric, 4-6.5 cm × ca. 7 mm; appendix narrowly conic, 15-45 × ca. 2 mm. Berry green, ca. 4 mm. Seeds few; synandria ca. 1 mm high, ca. 0.8 mm in diam. Fl. Feb-Apr (Yunnan), or Aug-Sep (Qin Ling area). 2n = 26, 28, 30, 36, 38, 42, 44, 46, 48, 52, 58, 84, 116.
Widely cultivated usually near farmhouses or in water fields; also naturalized or perhaps native in wet places in forests, valleys, swamps, wastelands, and at watersides. Anhui, Fujian, Guangdong, Guangxi, Guizhou, Hainan, Hubei, Hunan, Jiangsu, Jiangxi, Sichuan, Taiwan, Yunnan, Zhejiang [widely cultivated in tropics and subtropics].
This very variable species is widely cultivated throughout the tropics, and many wild or naturalized clones are found in S Asia, Malesia, and the Pacific islands. The spathes, spadices, and spadix appendixes vary considerably, although the floral organs have not been observed in many cultivated clones. This wide variation is attributable to cultivation selections, escapes, naturalizations, and re-domestications. It seems best, therefore, to treat Colocasia esculenta as a single species rather than formally recognize infraspecific taxa or segregate species (see Hay, Sandakania 7: 31-48. 1996).This very variable species is widely cultivated throughout the tropics, and many wild or naturalized clones are found in S Asia, Malesia, and the Pacific islands. The spathes, spadices, and spadix appendixes vary considerably, although the floral organs have not been observed in many cultivated clones. This wide variation is attributable to cultivation selections, escapes, naturalizations, and re-domestications. It seems best, therefore, to treat Colocasia esculenta as a single species rather than formally recognize infraspecific taxa or segregate species (see Hay, Sandakania 7: 31-48. 1996).
别名:coco yam;山芋;芋禾;芋渠;芋奶;芋苗;芋魁;芋头;野芋;芋头梗;青芋;红梗芋;高雄一号;狗爪芋;芋根;芋芨;毛芋子;接骨草;芋奶头;芋岌;毛芋艿;土芝;水芋;青皮叶;毛芋;毛艿;槟榔芋;毛芋头;蹲鸱;莒;独皮叶;芋艿;
科名:天南星科 Araceae
属名:芋属 Colocasia
2. 芋(名医别录) 芋头(各地),水芋(广东海南),芋岌、毛艿(指小块茎)、毛芋(福建 福州),青皮叶、接骨草、独皮叶(云南南部),土芝、莒(古称),蹲鸱(史记)
Colocasia esculenta (L). Schott, Melet. 1: 18. 1832; Kunth, Enum. Pl. 3: 37. 1841; N. E. Brown in Journ. Linn. Soc. Bot. 36: 183. 1903; 广州植物志: 639. 1956; S. Y. Hu in Dansk Bot. Arkiv 23 (4) : 428. 1968; 秦岭植物志1 (1) : 278. 1976. ——rum esculentum L., Sp. Pl. ed. 1: 965. 1753, ed. 2: 1369. 1763. Arum chinense L. in Amoen. Acad. 4: 234. 1754. ——Arum peltatum βLam. Encycl. 3: 13. 1789. ——Caladium esculentum vent., Hort. Cels. 30. 1800; Willd. , Spec. 4: 489. 1805.——Colocasia antiquorum var. esculenta (L.) Schott, Syn. Ar. 42. 1859; Engl. in DC., Monogr. Phan. 2: 492. 1879; Krause in Engl., Pflanzenr. 71 (4, 23E): 67. 1920. ——Caladium colocasia (L.) W. F. Wight ex Safford in Contr. u. s. Nat. Herb. 9: 206. 1905.
湿生草本。块茎通常卵形,常生多数小球茎,均富含淀粉。叶2-3枚或更多。叶柄长于叶片,长20-90厘米,绿色,叶片卵状,长20-50厘米,先端短尖或短渐尖,侧脉4对,斜伸达叶缘,后裂片浑圆,合生长度达1/2-1/3,弯缺较钝,深3-5厘米,基脉相交成30度角,外侧脉2-3,内侧1-2条,不显。花序柄常单生,短于叶柄。佛焰苞长短不一,一般为20厘米左右:管部绿色,长约4厘米,粗2.2厘米,长卵形;檐部披针形或椭圆形,长约17厘米,展开成舟状,边缘内卷,淡黄色至绿白色。肉穗花序长约10厘米,短于佛焰苞:雌花序长圆锥状,长3-3.5厘米,下部粗1.2厘米;中性花序长约3-3.3厘米,细圆柱状;雄花序圆柱形,长4-4.5厘米,粗7毫米,顶端骤狭;附属器钻形,长约1厘米,粗不及1毫米。花期2-4月(云南)至8-9月(秦岭)。
原产我国和印度、马来半岛等地热带地方。我国南北长期以来进行栽培。埃及、菲律宾、印度尼西亚爪哇等热带地区也盛行栽种,视为主要食料。由于芋最喜高温湿润,栽培习惯愈向南也就愈盛。
块茎可食:可作羹菜,也可代粮或制淀粉,自古视为重要的粮食补助或救荒作物,台湾省雅美族至今以芋为主粮。叶柄可剥皮煮食或晒干贮用。全株为常用的猪饲料。块茎入药可治乳腺炎、口疮、痈肿疗疮、颈淋巴结核、烧烫伤、外伤出血,叶可治荨麻疹、疮疥。▽本种很少开花,通常用子芋繁殖。
我国的芋,早在《史记》中即有记载:“岷山之下,野有蹲鸱,至死不饥,注云芋也。盖芋魁之状若鸱之蹲坐故也”。经劳动人民长期因地制宜地选种培育,已有多种不伺类型的品种,其中常见的为下列3类:▽1. 多头芋:母芋分蘖群生,子芋甚少,台湾山地栽培的狗蹄芋;广西宜山的狗爪芋皆属此类。特征:植株矮,一株生多数叶丛,其下生多数母芋,结合成一块;粉质,味如栗子。▽2. 大魁芋:母芋单一或少数,肥大而味美,生子芋少,植株高大,分蘖力强,子芋少,但母芋甚发达,粉质,味美,产量高。如台湾、福建、广东等热带地区常见的槟榔心、竹节芋、红槟榔心、槟榔芋、面芋、红芋、黄芋、糯米芋、火芋等。▽3. 多子芋:子芋多而群生,母芋多纤维,味不美。本类分蘖力强,子芋为尾端细瘦的纺锤形,易自母芋分离,栽培目的是采收子芋。我国中部及北部栽培者多属此类。如台湾的早生白芋,浙江杭州的白梗芋,浙江慈溪的黄粉芋等。浙江的红顶芋、乌脚芋、台湾的乌柿芋等品种具红色或紫色叶柄,也属此类。
《Flora of China》 Vol. 23 (2010)
Colocasia esculenta (Linnaeus) Schott in Schott & Endlicher Melet. Bot. 18. 1832.
芋 yu
Arum esculentum Linnaeus, Sp. Pl. 2: 965. 1753; A. colocasia Linnaeus; Caladium colocasia (Linnaeus) W. Wight; C. esculentum (Linnaeus) Ventenat; Calla gaby Blanco; Colocasia antiquorum Schott var. esculenta (Linnaeus) Schott ex Seemann; C. formosana Hayata; C. konishii Hayata; C. neocaledonica Van Houtte.
Rhizome vertical to horizontal, tuberous, 3-5 cm or more (up to 15 cm) in diam. Stolons long or absent. Leaves 2 or 3 or more; petiole green, 25-80 cm, sheathing for 1/3-2/3 length; leaf blade adaxially matte waxy-glaucous and water-shedding (water sometimes forming "mercury droplets"), oblong-ovate to suborbicular, 13-45 × 10-35 cm, base shallowly cordate (sinus 1-4 cm), apex broadly and shortly cuspidate. Peduncle usually solitary, 16-26 cm. Spathe tube green, 3.5-5 × 1.2-1.5 cm; limb open proximally, cream-colored to golden yellow, lanceolate or elliptic, 10-19 × 2-5 cm, apex acuminate. Spadix: female zone conic, 3-3.5 × ca. 1.2 cm; ovary 1-3 mm in diam.; stigma subsessile, narrower than apex of ovary; sterile zone narrowly cylindric, 3-3.3 cm; sterile flowers (pistils) seen from above elongate, ca. 0.5 mm in diam.; male zone cylindric, 4-6.5 cm × ca. 7 mm; appendix narrowly conic, 15-45 × ca. 2 mm. Berry green, ca. 4 mm. Seeds few; synandria ca. 1 mm high, ca. 0.8 mm in diam. Fl. Feb-Apr (Yunnan), or Aug-Sep (Qin Ling area). 2n = 26, 28, 30, 36, 38, 42, 44, 46, 48, 52, 58, 84, 116.
Widely cultivated usually near farmhouses or in water fields; also naturalized or perhaps native in wet places in forests, valleys, swamps, wastelands, and at watersides. Anhui, Fujian, Guangdong, Guangxi, Guizhou, Hainan, Hubei, Hunan, Jiangsu, Jiangxi, Sichuan, Taiwan, Yunnan, Zhejiang [widely cultivated in tropics and subtropics].
This very variable species is widely cultivated throughout the tropics, and many wild or naturalized clones are found in S Asia, Malesia, and the Pacific islands. The spathes, spadices, and spadix appendixes vary considerably, although the floral organs have not been observed in many cultivated clones. This wide variation is attributable to cultivation selections, escapes, naturalizations, and re-domestications. It seems best, therefore, to treat Colocasia esculenta as a single species rather than formally recognize infraspecific taxa or segregate species (see Hay, Sandakania 7: 31-48. 1996).This very variable species is widely cultivated throughout the tropics, and many wild or naturalized clones are found in S Asia, Malesia, and the Pacific islands. The spathes, spadices, and spadix appendixes vary considerably, although the floral organs have not been observed in many cultivated clones. This wide variation is attributable to cultivation selections, escapes, naturalizations, and re-domestications. It seems best, therefore, to treat Colocasia esculenta as a single species rather than formally recognize infraspecific taxa or segregate species (see Hay, Sandakania 7: 31-48. 1996).
- 寄生植物野菰对芭蕉芋的危害与防治
- 毛唇芋兰根茎的诱导与块茎形成
- 菊芋与蘘荷间作优质高产高效栽培技术
- 江篱属四种药用藻类微量元素含量测定
- 略谈番薯和薯蓣
- 广布芋兰的生药学研究
- NaCl胁迫对菊芋幼苗生长及其离子吸收运输的影响
- 海芋凝集素AML的原核表达及其多克隆抗体制备
- 高黎贡山斑龙芋(天南星科)
- 菊芋耐性胁迫及种质保存研究进展
- 香堂芋—黑塌菜栽培技术
- 不同激素对匙叶芋芽的诱导与增殖的影响
- 菊芋全粉凝胶特性的比较研究
- 不同品种菊芋对黄河三角洲土壤盐胁迫的响应研究
- 魔芋辐照接枝物凝胶的水分状态和结构分析
- 魔芋辐照接枝丙烯酸及其产物吸水性能的研究
- 不同浓度NaCl和Na2CO3处理对菊芋幼苗光合及叶绿素荧光的影响
- 从白魔芋未授粉子房培养出单倍体植株
- 魔芋属植物组织培养与遗传转化研究进展
- 花魔芋抗软腐病植株的鉴定及其抗性机理的初步研究
- 中国不产曲籽芋属植物
- 芋螺毒素氧化折叠研究进展
- 海洋生物药研发现状综述
- μ芋螺毒素基因的串联表达
- A-超家族芋螺毒素研究进展
- O-超家族芋螺毒素研究进展
- pH对魔芋胶复配体系凝胶特性及色泽的影响
- 芭蕉芋的性质及其淀粉的工业应用研究
- 魔芋葡甘聚糖的pH触发酶解
- 一步法发酵菊芋产乙醇菌种的筛选及产酶条件、酶学性质的研究
- 海芋过氧化氢酶的分离纯化及其性质
- 16份菊芋种质苗期耐盐碱性筛选与综合鉴定
- 设施条件下青菜间作大豆或芋艿控制斜纹夜蛾效果及对捕食性天敌多样性的影响
- 甘薯长喙壳侵染对甘薯块根抗氧化酶活性的影响
- 侵染天南星科植物病毒的分子鉴定及其生态学研究
- 三种前鳃亚纲海产腹足类性畸变现象的组织学研究
- 固氮类芽孢杆菌YUPP-5中环糊精糖基转移酶基因的克隆与功能分析
- PCR技术在海洋生物多肽毒素研究中的应用
- 魔芋葡甘露低聚糖的酶法制备工艺的初步研究
- 寡糖类能源植物菊芋及其综合利用研究进展
- 基于层次分析法和GIS的秦岭地区魔芋潜在分布研究
- 特异阻断乙酰胆碱受体的海南产α*-芋螺毒素的研究
- 芋螺毒素基因资源研究进展
- 灌水频率对河西走廊绿洲菊芋生活史对策及产量形成的影响
- 桶形芋螺和菖蒲芋螺的性畸变
- 不同浓度海水对菊芋幼苗生长及生理生化特性的影响(英文)
- 滨海半干旱地区海水灌溉对土壤安全和作物产量的影响
- 烟草和香芋上斜纹夜蛾的自然种群生命表
- 1-MCP和温度处理对采后芋头贮藏品质的影响
- 魔芋葡甘露聚糖及其衍生物在食品工业中的应用
- 提取野生向日葵DNA的新方法
- 辐照对魔芋葡甘聚糖溶解度及流变特性的影响
- 美国豆芋地上部位有效成分及α-葡萄糖苷酶抑制活性研究
- 芋营养器官中的草酸钙晶体及其可能的生理作用
- 广西柊叶属—新种
- 魔芋球茎细胞贮藏甘露聚糖粒的发育和内部结构(简报)
- 紫芋的组织培养与快速繁殖
- 浪心竹芋的离体培养和快速繁殖
- 彩云竹芋的离体培养和快速繁殖
- 碧浪竹芋的离体培养与快速繁殖
- 箭羽竹芋的离体培养和快速繁殖
- 尖尾芋的组织培养与快速繁殖
- 银叶竹芋的组织培养和快速繁殖
- 芋中多酚氧化酶的某些催化特性检测
- 岩芋的组织培养
- 海芋的组织培养与快速繁殖
- 珠芽魔芋的组织培养与快速繁殖
- 不同光照强度下花魔芋(Amorphophallus konjac)与谢君魔芋(Amorphophallus xiei)光合
- 江西铅山红芽芋脱毒苗球茎愈伤组织诱导及其再生体系的建立
- 氮肥对菊芋生物量、 热值和灰分含量的影响
- 莱州湾海涂海水灌溉菊芋的磷肥效应的研究
- 芋对氮磷钾吸收分配规律的研究
- 氮钾配施对芋头产量和品质的影响
- 云南魔芋新病害—疫病病原菌的鉴定
- 菊芋Na+/H+逆向转运蛋白基因的克隆与表达分析
- 菊芋生长发育动态及光合性能指标变化研究
- 碱胁迫对菊芋幼苗生长及其光合作用和抗氧化作用的影响
- 盐分和水分胁迫对菊芋幼苗离子吸收及叶片酶活性的影响
- 侵染我国芋的杆状DNA病毒分子鉴定及特异性检测
- 魔芋甘露聚糖化学结构的研究