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1.
利用传粉综合征预测:长瓣兜兰模拟繁殖地欺骗雌性食蚜蝇传粉 总被引:1,自引:0,他引:1
在花部进化受传粉者主导这一经典理论影响下,传粉综合征一直被认为是被子植物对应于某些特定传粉者的标志,因此,可以利用传粉综合征来预测传粉者。近年来,这种对应和预测受到多因素影响,以及花部进化理论和传粉者泛化理论的冲击。在本研究中,我们选择长瓣兜兰Paphiopedilum dianthum作为实验材料,来探讨传粉综合征与传粉者的关系以及利用前者预测后者的有效范围。长瓣兜兰具有的一系列特征,同其他依靠假繁殖地欺骗食蚜蝇传粉的兜兰种类相似,包括倒盔状唇瓣,较大的中萼片以及花瓣上的黑色突起和睫状毛,而且长瓣兜兰同这些种类有很近的亲缘关系和相似的生境。根据传粉综合征概念,长瓣兜兰应该是由食蚜蝇传粉,通过模拟繁殖地来欺骗传粉者。为了检验这些预测,我们对长瓣兜兰进行了传粉生物学研究。长瓣兜兰是自交可亲和的物种,不存在自动自交授粉现象,必须依靠昆虫传粉才能结实。结果表明,雌性黑带食蚜蝇Episyrphus balteatus是长瓣兜兰的主要传粉者,并且这种兜兰是通过模拟繁殖地来欺骗食蚜蝇传粉的。根据本实验结果,我们认为传粉综合征只是对应于不同的传粉选择压力而不是简单对应于传粉者种类,而使用传粉综合征预测时还需要考虑生境和演化历史等因素对花部形态的影响,这样才可能得到有效的结果。 相似文献
2.
国产兜兰属植物观赏价值评价及其在华南地区的应用前景分析 总被引:2,自引:0,他引:2
以植株的生长状况、整株姿态、叶片观赏性、开花性、花形、花色和花朵观赏期为评价指标,利用灰色关联分析,对我国原产的27种兜兰属植物的观赏价值进行了综合评价并分析了它们在华南地区的应用前景。结果表明:多花长瓣型的飘带兜兰与理想种的关联度最高,达到0.7304,是最值得在华南地区栽培的兜兰种类,其次为白旗兜兰。而紫纹兜兰、汉氏兜兰;文山兜兰、格利兜兰、带叶兜兰、亨利兜兰、同色兜兰,它们的关联度系数超过0.6;紫毛兜兰、巨瓣兜兰、红旗兜兰、天伦兜兰、长瓣兜兰、根茎兜兰的关联度均超过0.5;也是值得推广兜兰种类;杏黄兜兰、硬叶兜兰、白花兜兰由于生长状况差、开花性差等原因与理想种的关联度分别只有0.1900、0.1921、0.2917,不适于华南地区栽培;其它9种兜兰的关联度虽然介于0.35~0.50之间,但其中有些种类如虎斑兜兰、麻栗坡兜兰、波瓣兜兰、德氏兜兰等由于具有独特的观赏价值和育种潜力,也是值得在华南地区栽培的兜兰种类。 相似文献
3.
由于过度收集和对原生境地的破坏,我国野生兜兰已濒临灭绝,对其进行迁地保护十分必要。通过对引种的13种40份野生兜兰资源进行迁地栽培,并观测兜兰种质在迁移地的各种生长性状指标等,本研究利用灰色关联分析方法评价13种兜兰的迁地适应性,分析影响其迁地保护的关键因素。结果表明:(1)带叶兜兰、同色兜兰、长瓣兜兰、文山兜兰适应性较强,与理想种的关联度均在0.8以上;巨瓣兜兰、白花兜兰、小叶兜兰、紫纹兜兰、紫毛兜兰、硬叶兜兰适应性一般,与理想种的关联度在0.7~0.8之间;麻栗坡兜兰、杏黄兜兰、红旗兜兰适应性较差,与理想种的关联度均在0.6以下;(2)不同兜兰种类、同一种类不同产地兜兰种质的迁地生长适应性不同,来源地和栽培温度可能是影响其迁地保护的关键因子。 相似文献
4.
兰科(Orchidaceae)兜兰属(Paphiopedilum)植物花形奇特,研究价值和观赏价值都很高,对环境要求严格,是生物多样性保护中的“旗舰”类群。为掌握贵州省野生兜兰属植物资源现状和保护成效,该研究对野生兜兰属植物进行专项调查,对其资源量、分布格局、受威胁因素和就地保护等进行分析。结果表明:(1)共调查到8种兜兰属植物的103个分布点,分布于27个县,以南部、西南部为主要分布区,生境复杂多样,自然分布不均衡。(2)各物种分布面积从大到小的顺序为硬叶兜兰>小叶兜兰>麻栗坡兜兰>巨瓣兜兰>带叶兜兰>长瓣兜兰>白花兜兰>同色兜兰,资源丰富度从高到低的顺序为硬叶兜兰>小叶兜兰>带叶兜兰>巨瓣兜兰>麻栗坡兜兰>白花兜兰>长瓣兜兰>同色兜兰。(3)该类群受干扰因素复杂,受威胁较为严重,其中过度采挖、干旱、生境退化和破碎化是其濒危的主要原因。(4)该属“有效保护(EP)”2种,“较好保护(WP)”1种,“一般保护(GP)”2种,“较少保护(LP)”3种,未找到目标物种以致“保护状况不明(PSU)”2种。已调查到的物种保护率达100%,但分布点保护率仅29.13%,各物种分布点保护率差异显著; 建议相关部门有针对性地提升全省兜兰属植物的保护强度,进一步优化保护方式和范围,确保这些珍稀濒危的植物资源得到持续的生存发展。 相似文献
5.
报道了中国云南省兰科(Orchidaceae)兜兰属(Paphiopedilum)一新天然杂交种:哀牢山兜兰(Paphiopedilum×ailaoshanense B. Liu & S. P. Chen)。哀牢山兜兰与白旗兜兰(P. spicerianum)和沧源兜兰(P. gratrixianum var. cangyuanense)近缘,与前者的区别在于哀牢山兜兰花梗和子房有毛,中萼片带紫色晕以及紫色斑点,花瓣上侧暗绿色带紫色晕,下侧黄绿色;与后者的区别在于中萼片具1条宽阔的紫褐色中带,退化雌蕊紫色。哀牢山兜兰与天然杂种泸水兜兰(Paphiopedilum×lushuiense)相似,而哀牢山兜兰的中萼片下部边缘不后卷,近基部具紫红色晕,合萼片具2条明显紫色粗脉,花瓣匙形,上边缘波状,长6.0~6.2 cm,唇瓣长5.0~5.5 cm。为厘清哀牢山兜兰,沧源兜兰及白旗兜兰之间的关系,基于3个叶绿体基因片段(matK、rbcL、trnL),构建了兜兰属部分植物系统发育树。鉴于形态和分子数据,认为哀牢山兜兰是天然杂交种。凭证标本存放于福建农林大学标本馆。 相似文献
6.
对兜兰亚属(Paphiopedilum subgenus Paphiopedilum)12种植物的染色体数目和核型进行了研究。结果表明:这12种植物的染色体数目和核型存在差异,其中菲律宾兜兰(P. philippinense)的核型公式为2n=2x=26=16m+10sm, 长瓣兜兰(P. dithanum)为2n=2x=26=20m+6sm, 密毛兜兰(P. densissimum)为2n=2x=26=22m+4sm, 飘带兜兰(P. parishii)和带叶兜兰(P. hirsutissimum)为2n=2x=26=24m+2sm, 亨利兜兰(P. henryanum)、虎斑兜兰(P. markianum)和根茎兜兰(P. rhizomatosum)为2n=2x=26=26m, 而胼胝兜兰(P. callosum)为2n=2x=32=2M+24m+6sm, 布玲兜兰(P. microchilum)为2n=2x=38=28m+10sm, 卷萼兜兰(P. appletonianum)和海南兜兰(P. hainanensis)为2n=2x=38=30m+8sm。兜兰亚属的染色体主要为中部着丝粒染色体, 未见随体;最长染色体与最短染色体之比为2.07~3.44, 臂比大于2的染色体比率为0~0.231,核不对称系数为53.50%~58.95%。长瓣兜兰、飘带兜兰、亨利兜兰、密毛兜兰、虎斑兜兰、带叶兜兰和根茎兜兰等6种的核型类型为1B型,其余6种为2B型。 相似文献
7.
翡翠兜兰,中国云南兰科一新种 总被引:2,自引:0,他引:2
对兰科新种翡翠兜兰(Paphiopedilum smaragdinum)作了描述与绘图。新种产云南西部高黎贡山,与虎斑兜兰有亲缘关系,但花淡黄绿色无斑点和斑纹,退化雄蕊矩圆形,先端有短尖,短尖长1~1.5mm,易于区别。 相似文献
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CA Lei- CHEN Run-Zheng- YIN Zhi-Jian- ZHANG Guo-Xue- CHEN Wen-Hong- SHUI Yu-Min 《Plant Diversity》2015,37(6):733-736
A new species of Gesneriaceae from Honghe County, Southeastern Yunnan, China, Tremacron hongheense WH. Chen & YM. Shui, is described and illustrated. The new species is similar to Tremacron forrestii Craib, but differs by its leaf blade adaxially sparsely long setose (vs. densely white appressed pubescent and sparsely rusty brown villous), corolla tube outside short white glandular (vs. nearly glabrous), corolla lobes red and thickening at apex, especially adaxial lip (vs. yellow and not thickening), stamens 16-18cm long (vs. 04-12cm long), staminode 05-14cm long (vs. 02-04cm long). 相似文献
12.
在重庆市北碚区缙云山野外植物调查过程中,于海拔500~800 m的溪边阴湿沟谷中发现一种荨麻科植物,虽然该物种雌花序具花序托,但因其雌花花被片5枚,外面先端具角状突起,瘦果只具瘤状突起,更符合赤车属的特征,且结合分子系统学证据,该物种明显属于赤车属。该物种的特征在于其具花序托和总苞的雌花序,根据这一特征可将其置于头序赤车组(Sect.Elatostematopsis W.T.Wang),与头序赤车(Pellionia cephaloidea W.T.Wang)相似,但与后者区别在于其为草本,叶为羽状脉,侧脉在狭侧2~3条,宽侧3~4条,外层苞片2枚,无毛,背面具1绿色龙骨状突起,内层苞片8~12枚,无毛,背面具1绿色龙骨状突起,雌花花被片背面顶端具角状突起,瘦果椭圆形,具瘤状突起。基于形态学和分子系统学证据,特将它描述为赤车属一新种,命名为缙云赤车(Pellionia jinyunensis C.Xiong,F.Chen&H.P.Deng)。 相似文献
13.
The genus Acidosasa was published by the present authors in 1979. It only had one
species at that time, Acidosasa chinensis C. D. Chu et C. S. Chao. Since then species number
of the genus steadily increases. The authors have rather comprehensively studied this genus
and its related genera for F1. Reip. Pop. Sin. The present paper deals mainly with
morphological characteristics of the genus Acidosasa and the differences from its related genera i. e. Arundinaria, Sasa and Indosasa. The genus Acidosasa is closely related to the genus
Arundinaria in the type and origin of inflorescences and the vegetative appearance. But it differs from Arundinaria in the structure of florets. In Acidosasa, each floret is provided with six
stamens, while in Arundinaria each floret is of only three stamens. The genus Acidosasa is similar to the genera Indosasa and Sasa in the numbers of stamens, but it is distinguished from
lndosasa by its semelauctant (determinate) inflorescence, not iterautant (indeterminate) one,
from Sasa by its taller stature and branch complement with three branches.
We have carefully examined all the type specimens of Acidosasa and its related genera. A
conclusion reached is that there are six species in the genus Acidosasa, most of which are native to S. China, with only one species in Viet Nam. Five specific binomials are reduced and
one species is transferred into this genus. Two keys to species, respectively based on the flowering and vegetative characters, are given as follow:
Key to species of the genus A cidosasa (1)(based on the flowering state)
1. Lemmas glabrous.
2. Spikelets stout, 3-6mm broad, pedicels 1.5-4cm long; lemmas large, 1.5-2.2cm long,
with 15-19 nerves, subcoriaceous, not glaucous, shiny.
3. Lemmas up to 2.2cm long with conspicuously transverse veinlets, tessellate; palea and
rhachilla entirely. glabrous, lodicules elliptic-lanceolate, glabrous ... 1. A. chinensis
3. Lemmas 1.5-1.8cm. long, slightly tessellate; palea puberulous at apex of carina,
rhachilla puberuous at apex, lodicules obovate, ciliate at apex ............ 2. A. brilletii
2. Spikelets rather slende, 2-4mm broad, pedicels 0.5-1cm long; lemmas small, about
1.3 cm long, with 7-13 nerves, more or less glaucous .......... 3. A. chienouensis
1. Lemmas pubescent.
4. Glumas and lemmas densely pubescent ........................ 4. A. hirtiflora
4. Glumas subglabrous, lemmas sparsely pubescent.
5. Spikelets large, 3-7 cm long, lemmas 1.6-1.7 cm long, pedicels 2-13 mm long
................................................. 5. A. longiligula
5. Spikelets small, 2-3.7 cm long, lemmas about 1.3 cm long, pedicels 1-3 cm long
................................................... 6. A. venusta
Key to species of the genus A cidosasa (2) (based on the vegetative state)
1. Ligules of leaf-sheaths strongly elevated, usually 2-8 mm long.
2. Young culms with bristly sheath scars; culm-sheaths without auricles and oral
setae, not spotted, sheath-blades erect ................. 4. A. hirtiflora
2. Young culms with glabrous sheath scars; culm-sheaths with small auricles and oral
setae, sparsely spotted, sheath-blades reflexed .......... 5. A. longiligula
1. Ligules of leaf-sheaths inconspicuous, less than 2 mm long.
3. Young culms more or less bristly, or sheath-scars bristly:
4. Culm-sheaths without auricles and oral setae, not farinose, without hairs at base.
5. Young culms densely bristly; culm-sheaths attenuate at apex and as wide as sheath-blades, with conspicuously transverse veinlets; leaf-blades large, usually 2.5-3.5 (-6.5) cm broad, conspicuously tessellate
..................................................... 1. A. chinensis
5. Young culms sparsely bristly; culm-sheaths truncate at apex and broader than
sheath-blades, without transverse veinlets or inconspicuous; leaf-blades small,
1.5-2.5 cm broad, without visible transverse veinlets
.................................................... 6. A. venusta
4. Culm-sheaths with auricles and oral setae, slightly farinose, densely bristle at
base; leaf-blades rather narrow, 0.8-1.8 cm broad ............ 3. A. chienouensis
3. Young culms entirely glabrous; leaf-blades rather narrow, 1.2-1.8 cm broad ....................................................................................... 2. A. brilletill 相似文献
14.
描述了中国云南毛莨科Ranunculaceae一新种--哀牢山毛莨Ranunculus ailaoshanicus W.T.wang。此种在体态上与圆裂毛莨R.dongrergensis Hand.-Mazz.极为相似,但以茎较低矮,无叶,花较小,花瓣较小,长圆状椭圆形,脉不明显而相区别。 相似文献
15.
发表了云南高黎贡山西坡玉山竹属二新种:大玉山竹(Yushania gigantea Yi et L.Yang)和片马玉山竹(Yushania pianmaensis Yi et L.Yang)。大玉山竹近似西藏玉山竹(Y.xizangensis Yi),不同在于秆柄粗壮,直径7~12 mm,节间长达2.5 cm;秆较高大,高6~7 m,节间分枝一侧基部扁平或具短纵沟槽;小枝具(5)6(7)叶;叶鞘较长,长(2.5)3.2~4.8 cm;叶柄无毛;叶片较大,长(3.5)10~ 18(20) cm,宽(4.5)8~13(18) mm,易于区别。片马玉山竹相似大玉山竹(Y.gigantea Yi et L.Yang),但本种秆较矮小,高2.5~4 m,直径1~1.8(2.5) cm;枝条较多而细,在秆上每节12~30枚,直径1~1.5(2) mm;箨鞘背面无毛,箨片较小,长1.5~3.5 cm,宽1~2.5 mm;小枝具叶较少,为(3)4~5枚;叶片较小,长达12.5 cm,宽达8 mm。 相似文献
16.
该文描述了自云南东南部发现的荨麻科楼梯草属二新种。(1)文山楼梯草,与上林楼梯草在亲缘关系上相近,与后者的区别在于本种的茎密被短柔毛,叶片在基部斜楔形,具半离基三出脉,雌头状花序的花序托较小,长约1.2 mm,宽1 mm,不分裂,其雌苞片约12,不等大,只3枚在顶端具角状突起。(2)绿突楼梯草,与马关楼梯草近缘,与后者的区别在于茎密被反曲的柔毛和贴伏的短柔毛,雄花序较长,雄总苞的苞片6枚,排成2层,2外层苞片较大,背面具1绿色纵列龙骨状突起和4或6绿纵肋,4内层苞片较小,背面近中央有1绿色角状突起。 相似文献
17.
Lysionotus fengshanensis Yan Liu & D. X. Nong, a new species of Gesneriaceae from Guangxi, China, is described and illustrated. Lysionotus fengshanensis is very similar to L. longipedunculatus (W. T. Wang) W. T. Wang, but differs by the peduncle being 2–4 cm long and purple, corolla campanulate, 2.5–3.0 cm long, 1.5–1.7 cm in diameter at the mouth, filaments slightly geniculate near the middle, apex of filaments with gland and staminodes 3. 相似文献
18.
Pan Jin-Tang 《植物分类学报:英文版》1986,24(3):203-214
This paper deals with the taxonomy and geographic distribution of the genus Chrysosplenium L. in China.
Based on the characters and evolution of the seed, capsule, disk, ovary and leaf, the
species of this genus can be grouped into 2 subgenera, 5 sections and 16 series. There
are 2 subgenera, 5 sections and 11 series in China. They are as follows:
I. Subgen. Gamosplenium Maxim. emend. J. T. Pan
Leaves alternate.
Lectotype: Chrysosplenium carnosum Hook. f. et Thoms.
1. Sect. Alternifolia Franch. emend. J. T. Pan
Seeds smooth and glabrous.
Type: Chrysosplenium alternifolium L.
(1) Ser. Nudicaulia Maxim. emend. J. T. Pan
Disk obscure or absent; ovary nearly half-inferior, sometimes mostly inferior; capsule generally subtruncate and emarginate at top and bilobed with equal and horizontally divaricate or suberect lobes; seeds smooth and glabrous.
Type: Chrysosplenium nudicaule Maxim.
(2) Ser. Alternifolia Maxim. emend. J. T. Pan
Disk 8-lobed; ovary nearly half-inferior; capsule generally subtruncate and emarginate at top, and bilobed with equal and horizontally divaricate lobes; seeds smooth
and glabrous.
Type: Chrysosplenium alternifolia L.
2. Sect. Nephrophylloides Turcz.
Seeds minutely papillose or pilose.
Type: Chrysosplenium sedakowii Turcz.
(1) Ser. Macrophylla Franch. emend. J. T. Pan
Disk obscure or absent; ovary nearly half-inferior; capsule nearly truncate and emarginate at top, and bilobed with equal lobes; seeds minutely papillose.
Type: Chrysosplenium macrophyllum Oliv.
(2) Ser. Ovalifolia Maxim. emend. J. T. Pan
Disk generally 8-, rarely 4-, lobed, papillae absent around disk; ovary mostly inferior; capsule subtruncate and emarginate at top; seeds minutely papillose or pilose.
Type: Chrysosplenium ovalifolium M. Bieb. ex Bunge
(3) Ser. Lanuginosa Hara, emend. J. T. Pan
Papillae numerous, brown around reduced disk; ovary mostly inferior; capsule nearly truncate and emarginate at top; seeds minutely papillose.
Type: Chrysosplenium lanuginosum Hook. f. et Thoms.
II. Subgen. Chrysosplenium
Leaves opposite.
Type: Chrysosplenium oppositifolium L.
1. Sect. Trichosperma J. T. Pan, sect. nov.
Capsule not truncate at top, and bilobed with subequal, suberect or divergent lobes.
Type: Chrysosplenium trichospermum Edgew. ex Hook. f. et Thoms.
This section is divided into 4 series in the world, with only 1 in China.
(1) Ser. Nepalensia Maxim. emend. J. T. Pan
Disk obscure or absent; ovary generally mostly inferior; cassule not truncate at
top, and bilobed with subequal and suberect or divergent lobes; seeds smooth and glabrous.
Type: Chrysosplenium nepalense D. Don
2. Sect. Grayana J. T. Pan, sect. nov.
Capsule bilobed with distinctly unequal and ascending lobes.
Type: Chrysosplenium grayanum Maxim.
This section consists of 4 series in the world, with 3 series in China.
(1) Ser. Sinica Maxim. emend. J. T. Pan
Disk obscure or absent; ovary nearly half-superior; capsule bilobed with distinctly
unequal and ascending lobes; seeds minutely papillose.
Type: Chrysosplenium sinicum Maxim.
(2) Ser. Esulcata Franch. emend. J. T. Pan
Disk (4)-8-lobed; ovary generally half-inferior; capsule bilobed with unequal and
ascending lobes; seeds minutely papillose or pilose.
Lectotype: Chrysosplenium dubium J. Gayex DC.
(3) Ser. pilosa maxim. emend. J. T. Pan
Disk obscure or absent; ovary nearly half-inferior; capsule bilobed with distinctly
unequal and ascending lobes; seeds distinctly longitudinally ll-18-costate and minutely papillose or tuberculate on the ridge.
Type: Chrysosplenium pilosum Maxim.
3. Sect. Chrysosplenium
Capsule nearly truncate and emarginate at top, and bilobed with equal and horizontally divaricate lobes.
Type: Chrysosplenium oppositifolium L.
(1) Ser. Romosa J. T. Pan, ser. nov.
Disk distinctly 8-lobed, papillae sparse, brown around disk; ovary mostly inferior; capsule nearly truncate and emarginate at top, and bilobed with equal and horizontally
divaricate lobes; seeds smooth and glabrous.
Type: Chrysosplenium ramosum Maxim.
This series is monospecific one, also occurring in China, namely C. ramosum Maxim.
(2) Ser. Delavayi Hara
Disk distinctly 8-lobed, Papillae sparse, brown around the disk; ovary mostly inferior; capsule nearly truncate and emarginate at top, and bilobed with equal and horizontally divaricate lobes; seeds distinctly longitudinally 10-16-costate and transversely striate on the ridge.
Type: Chrysosplenium delavayi Franch.
This series can be considered as the most advanced one in the Chrysaspleninm L.
So far, the Chrysosplenium L. comprises 64 species in the world, among which 1 species is found in North Africa, 2 in South America, 4 in Europe, 5 in North America, 56
in Asia, of which 3 occur in Sikkim, 5 Bhutan, 5 Mongolia, 6 north Burma, 6 Korea, 7
north India, 8 Nepal, 12 Japan, 17 U.S.S.R. (of which 3 also in Europe), 34 China (including 22 endemic species and 3 new species).
In China, Fujian and Guangdong Provinces and Zhuang Autonomous Region of Guangxi each has only 1 species, Taiwan, Zhejiang, Shanxi and Hebei Provinces and Uygur Autonomous Region of Xinjiang each has 2, Anhui, Jiangxi and Hunan Provinces
each has 3, Qinghai Province 4, Heilongjiang, Liaoning and Guizhou Provinces each has
5, Jilin and Hubei Provinces each has 6, Gausu Province 8, Shaanxi Province and Xizang (Tibet) Autonomous Region each has 10, Yunnan Province has 11, Sichuan Province has 14.
Thus the distribution centre of this genus should be in the north temperate zone
of Asia, and the region covering Shaanxi Gansu, Sichuan, Yunnan and Xizang may be
regarded as an important part of this centre.
The 7 species of Ser. Nudicaula Maxim. emend. J. T. Pan can be considered as the
most primitive ones in this genus. They are mostly distributed in Shaanxi (Qin Ling),
south Gansu, southeast Qinghai, southwest Sichuan and nothwest Yunnan of China. This
region may be considered as the centre of the origin (or at least differentiation) of this
genus.
The new species and the new varieties described in this paper are as follows: C. hydrocotylifolium Levl. et Vant. var. emeiense J. T. Pan, C. taibaishanense J. T. Pan, C.
lixianense Jien ex J. T. Pan, C. qinlingense Jien ex J. T. Pan. 相似文献
19.