獐牙菜属植物花蜜腺形态及解剖学

在扫描电镜下观察了獐牙菜属Swertia L.10组30种植物花蜜腺的数目,位置,形态和附属物等特征;同时还利用光镜对各组代表种的蜜腺结构进行了解剖学观察。结果表明獐牙菜属花蜜腺外部形态多种多,但在组与组之间无明显间断,演化序列呈梯度变化;内部结构基本相同,为不具维管束的结构蜜腺,且均为淀粉型蜜腺。因此,从花蜜腺的角度不支持将獐牙菜属划分为小属的观点,同时,还结合其它证据讨论了花蜜腺特征的演化趋势。     

“藏茵陈”的基原植物和药用亲缘学

详细比较藏药"藏茵陈"基原植物川西獐牙菜及其混淆品(代用品)抱茎獐牙菜、紫红獐牙菜、四数獐牙菜、红直獐牙菜、大籽獐牙菜、狭叶獐牙菜和椭圆叶花锚的外部形态特征及化学成分,澄清了这一类群在分类上的混乱,发现川西獐牙菜与紫红獐牙菜在习性,花部特征,种子形态和化学成分组成等方面相似性最高,印证了核基因ITS序列的结果。同时分析"藏茵陈"混淆的原因是多种来源和形态相似性造成的,讨论了"藏茵陈"鉴定的方法。通过对獐牙菜属系统关系的分析,提出紫红獐牙菜作为川西獐牙菜替代品的理论依据。     

2种藏茵陈类植物的引种地繁殖系统研究

通过观察、套袋、人工授粉对引种至低海拔栽培地的2种藏茵陈"类植物——川西獐牙菜(Swertia mus-sotii)和抱茎獐牙菜(S.franchetiana)繁育系统进行研究.结果表明:(1)引种的2种植物均为雌雄同株、自交亲和,但大部分花雌雄异熟(dichogamy)和雌雄异位(herkogamy),雌雄同熟的比例为24%,且雌雄同熟的雄蕊群远离雌蕊,需要靠传粉昆虫等传粉媒介传粉.(2)引种到低海拔的2种藏茵陈"类植物结实率和发芽率均较高,其中川西獐牙菜柱头张开第2天的授粉结实率达76.54%,种子发芽率达84.29%.(3)低海拔栽培的川西獐牙菜的传粉昆虫是家养蜜蜂,抱茎獐牙菜的开花时间较川西獐牙菜晚20 d,有效的传粉昆虫由家养蜜蜂变成一种很小的蜂类.研究表明,川西獐牙菜和抱茎獐牙菜由高海拔引种到低海拔地区后,结实率和种子发芽率均较高,可以用引种栽培的方式进行藏茵陈"药材的繁殖.     

基于不同DNA序列对四数獐牙菜系统位置分析

以扁蕾属植物为外类群,基于trnL-trnF序列、rpl16序列以及 ITS序列,采用最大简约法对四数獐牙菜的系统位置进行了分析.结果显示:尽管在ITS系统发育树、trnL-trnF系统发育树和rpl16系统发育树中所用的种和数量有所不同,所得到的3种系统发育树的拓扑结构也不一致,但四数獐牙菜的系统位置在3种系统发育树中的结果基本一致.在trnL-trnF系统发育树中,四数獐牙菜与花锚属的H.elliptica、H.brevicornis和H.weddelliana形成了一个单系群;而在ITS和rpl16系统发育树中,四数獐牙菜与歧散獐牙菜先聚在一起,再与花锚属的植物聚为一支支持率较高的单系支.研究表明,四数獐牙菜与Anagalidium属的歧散獐牙菜的亲缘关系最近,其次是与花锚属的植物,而与獐牙菜属植物的亲缘关系较远.本实验系统发育的结果支持将四数獐牙菜从獐牙菜属中分出而归入Anagalidium属的观点.     

四数獐牙菜的胚胎学及其系统学意义

四数獐牙菜花药四室,药壁发育为双子叶型;绒毡层腺质型。小孢子母细胞减数分裂为同时型, 四分体的排列方式为四面体形;成熟花粉为3-细胞。子房2心皮,2心皮连接处强烈内凸,4列胚珠。薄 珠心,单珠被,直生胚珠。胚囊发育为蓼型。胚乳发育为核型。胚胎发育为茄型酸浆I变型。反足细胞 在胚囊成熟时期宿存。果实成熟时,种子只发育至球型胚阶段。承珠盘存在。与已研究的獐牙菜种类 的胚胎特征相比较,该种存在三个显著的特点：直生胚珠,心皮连接处强烈内凸,承珠盘存在。这三个特 征目前仅在龙胆族中的花锚属中发现。经过性状分析,它们均是演征,此三个共有演征表明四数獐牙菜 与花锚属是一单系群,它们的亲缘关系最近。这与Yun &; Kupfer(1995)的分子证据部分吻合,因为分 子系统树上的花锚单系支包括花锚、四数獐牙菜和北美的密花属(广义獐牙菜属中的密花组),而后者的 胚胎学特征未有任何报道。胚胎学研究暗示四数獐牙菜的分类学等级有待重新评价,广义的獐牙菜属 有可能不是一单系发生群。     

獐牙菜属5种植物的核型研究

首次报道了中国５种獐芽菜属植物的染色体数目和核型。它们染色体中期核和相对长度组分分别是：四数獐牙菜为２ｎ＝１４＝４ｍ＋８ｓｍ＋２ｓｔ＝２Ｌ＋６Ｍ２＋４Ｍ１＋２Ｓ;华北獐牙菜２ｎ＝２８＝１２ｍ＋１４ｓｍ＋２ｓｔ＝６Ｌ＋８Ｍ１＋＋６Ｓ;二叶獐牙菜为２ｎ＝２８＝１４ｍ＋４ｓｍ＋１０ｓｔ＝２Ｌ＋１４Ｍ２＋１０１＋ｓＳ;抱茎獐 菜为２ｎ＝６ｍ＋１２ｓｍ＋２ｓｔ＝８Ｍ２＋１２Ｍ;浙江獐牙菜为２ｎ＝２０＝８ｍ＋     

人工栽培与野生种抱茎獐牙菜矿物元素和氨基酸对比分析

抱茎獐牙菜又称藏茵陈,是藏药中常用草药,广泛应用于肝胆疾病的治疗。近年来,为满足日益增加的需求量,发展了人工栽培抱茎獐牙菜,研究比较人工栽培与野生抱茎獐牙菜之间的各种成分含量,对人工栽培抱茎獐牙菜替代野生抱茎獐牙菜用药有重要意义。本文对人工栽培及野生抱茎獐牙菜的矿物元素及氨基酸进行测定比较发现,人工栽培抱茎獐牙菜的矿物元素绝大多数比野生抱茎獐牙菜含量高,人工栽培抱茎獐牙菜氨基酸大多比野生抱茎獐牙菜含量高。     

4种秦艽属植物不同器官中4种环烯醚萜苷成分含量的比较分析

利用HPLC法测定了秦艽(Gentiana macrophylla Pall.)、粗茎秦艽(G.crassicaulis Duthie ex Burk.)、麻花秦艽(G.straminea Maxim.)和小秦艽(G.dahurica Fisch.)根、茎、叶和花中4种环烯醚萜苷成分(包括马钱苷酸、獐牙菜苦苷、龙胆苦苷和獐牙菜苷)的含量,并对来源于不同产地秦艽和小秦艽不同器官4种环烯醚萜苷成分的含量进行了比较。结果显示:4种秦艽属植物不同器官4种环烯醚萜苷成分含量差异明显,来源于3个产地(陕西太白、甘肃西河乡和马狭)的秦艽和2个产地(青海互助和陕西麟游)的小秦艽不同器官中4种环烯醚萜苷含量也均具有明显差异。4种秦艽属植物根、茎、叶和花中龙胆苦苷和马钱苷酸总量分别为质量分数5.996%～10.869%、0.310%～4.065%、0.235%～4.138%和0.545%～5.591%;根中獐牙菜苦苷和獐牙菜苷的质量分数分别为0.516%～0.953%和0.042%～0.210%,茎中分别为0.173%～0.383%和0.031%～1.700%,叶中分别为0.068%～0.684%和0.020%～3.208%,花中分别为0.460%～0.832%和0.138%～3.827%。粗茎秦艽各器官龙胆苦苷和马钱苷酸总量均最高,小秦艽各器官龙胆苦苷和马钱苷酸总量均最低,总体上,秦艽和粗茎秦艽中龙胆苦苷和马钱苷酸总量高于小秦艽和麻花秦艽;小秦艽茎、叶和花中獐牙菜苷含量均最高,而秦艽茎和叶及粗茎秦艽花中獐牙菜苷含量均最低。4种秦艽属植物根部龙胆苦苷和马钱苷酸含量均明显高于茎、叶和花,獐牙菜苦苷在根和花中的积累较多,獐牙菜苷在花中的含量均相对最高。产自青海互助的小秦艽茎、叶和花中獐牙菜苷含量均最高,质量分数分别为2.884%、5.215%和7.321%。研究结果表明:4种环烯醚萜苷成分含量不但与植物种类和器官有关,而且与产地和采样时间也有关。     

獐牙菜属植物叶表皮特征

利用光学显微镜观察了獐牙菜属３５种植物的呈表皮,发现该属植物成熟叶上下表皮细胞形状（表面观）为多边形和不规则型,垂周壁式样为平直、弓形和波纹,多数种类上、下表皮均有气孔器分布,气顺类型主要有３种,无规则型,不等型和平列型。这些特殊２对獐牙菜属下分类有一定的意义。结合其它方面的研究成果,初步确定叶表皮特征可能具有以下演化趋势,垂周壁式样深波方←浅波纹→平直,弓型,气顺类型无规则型→不等型→平列型。     

藏药抱茎獐牙菜HPLC指纹图谱研究

采用反相高效液相色谱-二极管阵列的检测方法,对不同产地的10批野生和栽培抱茎獐牙菜药材的水溶性成分进行了分析,建立了抱茎獐牙菜药材的指纹图谱.色谱柱为VP-ODSC18柱 5μm,150mm×4.6mm ,流动相为甲醇-0.02%的磷酸水溶液,检测波长254nm.用文中的最佳条件可较全面地反映抱茎獐牙菜的主要成分,为藏药抱茎獐牙菜的质量控制提供了科学依据.     

Embryology of Swertia (Gentianaceae) relative to taxonomy

The embryological features of three species of Swertia ( s.l.) – S. erythrosticta , S. franchetiana , and S. tetraptera – were characterized, and the observations were used, together with previously gathered data on other species, to evaluate a recently proposed polyphyly, based on molecular data, of Swertia s.l. Comparisons of species within the genus showed that they have diversified embryologically, and there are significant between-species differences. Notable features that vary between species include the number of cell layers that form the anther locule wall, the construction of the wall of the mature anther, tapetum origin, the cell number in mature pollen grains, the structure of the fused margins of the two carpels, the ovule numbers in placental cross-sections, the shape of the mature embryo sac, the degree of ovule curvature, antipodal variation and the presence of a hypostase, and seed appendages. They share characters that are widely distributed in the tribe Gentianeae, such as a dicotyledonous type of anther wall formation, a glandular tapetum with uninucleate cells, simultaneous cytokinesis following the meiosis of the microsporocytes, tetrahedral microspore tetrads, superior, bicarpellary and unilocular ovaries, unitegmic and tenuinucellar ovules, Polygonum -type megagametophytes, progamous fertilization, nuclear endosperm, and Solanad-type embryogeny. The presence of variation in embryological characters amongst the species of Swertia s.l. strongly supports the view that Swertia s.l. is not a monophyletic group. Frasera is better separated from Swertia s.l. as an independent genus, and is only distantly related to Swertia s.s. judging from the numerous differences in embryology. Swertia tetraptera is very closely related to Halenia , as they show identical embryology.  © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society , 2007, 155 , 383–400.     

群心菜花蜜腺的发育解剖学研究

群心菜（Ｃａｒｄａｒｉａｄｒａｂａ（Ｌ．）Ｄｅｓｖ）花蜜腺６枚,包括４枚侧蜜腺的和２枚中蜜腺,属十字花科侧中蜜腺类型中的侧分离中间亚型,侧中蜜腺结构相同,都由分泌表皮,产蜜组织组成,分泌表皮顶部分布的有变态气孔器,产蜜组织中无维管束分布,属较原始的十字花科花蜜腺亚型类型,在花的各部分基本分化完成后,由花托表层细胞恢复分裂能力形成蜜腺原基,蜜腺原基经分裂,分化和形态建成,发育形成成熟蜜腺,侧中蜜腺发     

垂柳花蜜腺的发育解剖学研究

垂柳雌花蜜腺一枚,位于于房与花序轴之间,多呈扁平广卵形,由分泌表皮、泌蜜组织和维管束组成。雄花蜜腺呈基部相连的两枚突起,一枚位于花丝与花序轴之间,基部宽扁,上部棒状;另一枚位于花丝与苞片之间,棒状,仅由分泌表皮和泌蜜组织组成。雌、雄花蜜腺均起源于花托表面2—3层细胞。在蜜腺发育过程中,雌、雄花蜜腺泌蜜组织细胞的液泡发生规律性变化．雌花蜜腺为淀粉型蜜腺,而雄花蜜腺为非淀粉型蜜腺。雌、雄花蜜腺的原宜汁分别由蜜腺维管束韧应部或花丝维管束韧皮部提供,其蜜计最后均由分泌表皮细胞和变态气孔排出。     

芝麻菜花蜜腺的结构和发育研究

通过解剖镜观察、石蜡切片和薄切片等方法,对芝麻菜的花蜜腺的位置、形态、结构、发育过程及泌蜜前后组织化学变化进行了研究。芝麻菜花蜜腺4枚,分成两对,其中一对侧蜜腺较大,棱柱状,分别着生在外轮2个短雄蕊基部内侧的花托上,结构上由表皮、产蜜组织和维管组织构成;另一对中蜜腺较小,近棒状,分别着生在内轮4个长雄蕊外侧的花托上,结构上仅由表皮和产蜜组织构成。二者表皮细胞外都具角质层,且蜜腺产蜜组织细胞中只含少量的多糖物质。两类蜜腺的蜜汁均由变态气孔泌出体外。无论侧蜜腺还是中蜜腺,蜜腺原基皆是在雌、雄蕊已分化后,由花托相应位置表皮下的1～2层细胞分裂形成的。在蜜腺发育中,产蜜组织细胞在泌蜜前后不具明显的液泡变化。     

密花香薷花蜜腺的解剖学研究

密花香薷花密腺分布于子房基部和子房表面,属于一朵花中具二种花蜜腺类型,子房基部的盘状蜜腺由分泌表皮、产蜜组织及维管束三部分组成,分泌表皮上角质层局部有小孔。子房蜜腺由分泌表皮和产蜜组织组成。     

Anatomy of the floral nectaries of some neotropical Salacioideae (Celastraceae)

Floral nectaries have contributed to the systematics of different taxonomic groups. Since those of the neotropical genera included in subfamily Salacioideae—Cheiloclinium Miers, Peritassa Miers, Salacia L. and Tontelea Aubl.—have different forms and positions, we explored their anatomy to delimit more precisely the genera of subfamily Salacioideae. Buds and open flowers of six species were treated following the usual techniques in plant anatomy. The obtained data were helpful in characterizing the floral nectary anatomy of the studied species. Furthermore, some features such as form, position and surface of nectaries; form of their epidermal cells; presence and distribution of stomata; occurrence of idioblasts containing druses in the nectariferous parenchyma; and absence of nectary vascularization can contribute to the taxonomy and phylogeny of the Salacioideae studied. In most of the studied species the nectar is probably released by both the stomata and the nectary epidermal surface. In Cheiloclinium cognatum, the structure acknowledged as nectary is actually a vestigial tissue and the functions of attracting and rewarding pollinators has phylogenetically migrated to the stigmatic region. The druses and phenolic substances observed in the nectariferous parenchyma probably help defend flowers against herbivore attacks. The minute size of the nectaries of Salacioideae may explain the absence of vascularization. The floral nectaries of Salacia elliptica are epithelial while those of the other species are mesenchymal.     

短果大蒜芥花蜜腺的发育解剖学研究

短果大蒜芥（Sisymbrium loeselii L.var.brevicarpum Z.X.An)花蜜腺位于雄蕊基部花托上,属十字花科环状花蜜腺类型中的侧棱环四圆环亚型。蜜腺由分泌表皮,产蜜组织和维管束组成。分泌表皮上有变态气孔器,蜜腺中部的气孔器呈舟状分布。产蜜组织中的维管束来自于花托中的维管束分支,属较进化的十字花科花蜜腺的亚型类型。蜜腺原基是在花的各部分原基分化后,由雄蕊基部花托表面区域的2－3层细胞,经反分化形成,环状蜜腺发生发育同步,在蜜腺的发育过程中,蜜腺组织中的液泡和淀粉粒都发生了有规律的变化,其原蜜汁由维管束提供,运转至产蜜组织,最后由变态气孔泌出。     

长药景天花蜜腺的发育解剖学研究

长药景天花蜜腺５枚,呈侧向扁平的舌形或弯月形,分别位于５株离生心皮的外侧,两者的基部相连,属于子房蜜腺。蜜腺由分泌表皮、产蜜组织和仅含韧皮部的维管束组成。长药景天花蜜腺起源于心皮外侧基部的表层结构。产蜜组织在发育过程中,细胞中的液泡体积及淀粉粒呈现有规律的消长变化。泌蜜后期,蜜腺组织从上往下液泡化,具明显的方向性。根据其结构及多糖变化分析,来自韧皮部的原蜜汁以淀粉粒形式贮存于产蜜组织中,泌蜜期水解     

Developmental and Anatomical Studies on the Floral Nectaries of Capsella bursa-pastoris

The development and structure of the floral nectaries of Capsella bursa-pastoris (L.) Medic. were examined. The nectaries consisted of four separated parts which were semiorbicular and were morphologically and anatomically similar to one another. They were located at the receptacle between stamens, and each part was composed of secretory epidermis, nectariferous tissue and vascular bundles, belonging to structural nectary. When the various floral organs were developed, 2--3 superficial layer cells of the receptacle between stamens became meristemoid and contributed to primordia the formation of nectary. By intercalary meristematic activity, the four nectaries formed synchronously. During the different stages of nectary differentiation, the content of starch gra ins and vacuolation in the cells of epidermis and nectariferous tissue changed regularly. According to the structural and histochemical changes the pre-nectar might be supplied by phloem. The nectar formed in nectariferous tissue was then secreted to the sub-stomatal chamber and where it was finally excreted from the stoma.