中国侧棘斑蚜属(蚜科,角斑蚜亚科)地理分布格局研究

用GIs技术研究斑蚜科侧棘斑蚜属Tuberculatus在中国的地理分布格局。种类以县级行政单元转换地理坐标与动物地理区划图叠加后产生蚜虫地理分布图。结果显示出这个属主要分布在东北区南部、华北区、华中区、华南区和西南区东部(中国南部和东部)。根据地理分布图及有关统计分析,认为东北区南部—华北区北部和华中区南部一东南部是这个属在中国的分布中心、分化中心和特有中心。同时,利用寄主植物的分布,探讨了中国侧棘斑蚜属的分布与寄主植物分布之间的关系。     

中国潜跳甲属分类研究(鞘翅目:叶甲科:跳甲亚科)

本文系统研究了潜跳甲属Podagricomela Heikertinger的中国种类,共10种,包括1新记录种：黑足潜跳甲P.nigripes Medvedev。文中提供了分种检索表、简要描述和雌雄外生殖器特征图。在此基础上对本属在中国的地理分布格局进行了初步探讨。潜跳甲属Podagricomela Heikertinger的分布中心在中国,表现出由南向北分布的特点,主要分布于华南区、西南区、华中区和华北区,多以芸香科植物为寄主。     

中国瘿绵蚜属的地理分布(同翅目：瘿绵蚜科)

以中国分布的２５种瘿绵蚜属Ｐｅｍｐｈｉｇｕｓ蚜虫为材料,研究了瘿绵蚜属在中国的分布特点。结果表明,该属蚜虫在古北界和东洋界均有分布,但古北界占绝对优势。在中国昆虫地理区划中,７个区均有分布,但以华北区和青藏区最为丰富,华中区和华南区最少。除华中区和华南区外,各区均有特有成分分布,县以华北区和青藏区最盛。由于没有明显的地理阻隔,华北区、东北区、蒙新区之间有种类交流现象存在,而它们与青藏区和西南区之间     

核桃扁叶甲三亚种的分类地位订正 (鞘翅目：叶甲科，叶甲亚科)

通过对核桃扁叶甲3个亚种（指名亚种Gastrolina depressa depressa Baly,淡足亚种G. depressa pallipes Chen和黑胸亚种G. depressa thoracica Baly）的比较形态学研究,结合生物学和生物地理学方面的资料,对其分类地位进行了探讨。从形态上来说,三者的上唇、下唇、后翅和爪的形态区别较小,但是触角、上颚、下颚和受精囊则存在着较大的区别,而且通过超微形态的比较,淡足亚种、黑胸亚种和指名亚种均存在着较为明显的形态区别。动物地理学研究表明,指名亚种和黑胸亚种在我国北纬25°～30°之间有地域重叠,目前仅在部分地区可以通过海拔来区分。但是对于淡足亚种而言,它的分布区与其他两个亚种有着一定的地理隔离,其间并没有重叠区的存在。因此从地理分布上而言,三者也存在着不同。通过上述讨论,本文将核桃扁叶甲三亚种恢复或提升为种,即核桃扁叶甲G. depressa Baly,黑胸扁叶甲G. thoracica Baly和淡足扁叶甲Gastrolina pallipes Chen, stat. Nov.。     

中国高山萤叶甲区系研究

讨论的高山萤叶甲系指分布在海拔２５００ｍ以上的中国种类,总计１３１种,分隶于４９属,分别占萤叶甲亚科我国已知种,属的１／６和１／２,其分布区域以青藏高原,特别是横断山区种,属分布最为密集。部分属,种也涉及到台湾,而且表现出台湾与中国西部横断山区间断分布现象。     

额凹萤叶甲属一新种(鞘翅目:叶甲科, 萤叶甲亚科)

额凹萤叶甲属 Sermyloides 属鞘翅目(Coleoptera)叶甲科(Chrysomelidae)、萤叶甲亚科(Galerucinae)。它以头部额唇基区凹陷、其中有一些隆起为属的主要特征,是典型的东洋区分布属。目前本属世界已知21种,主要分布于东南亚及我国南方,本文又增     

中国大萤叶甲属的研究（鞘翅目：叶甲科：萤叶甲亚科）

大萤叶甲属Meristata 为Chapuis 1875年所建立,是东洋区分布的属,在我国主要分布在云南和西藏两省,中名以其体大型而得。目前全世界已知11种,中国有9种。本文对本属征进行了重新厘订,并对中国种类做了系统的研究及记述,它们是褐大萤叶甲Meristata dohrni (Baly), 长大萤叶甲Meristata elongata (Jacoby), 黑斑大萤叶甲Meristata fallax (Harold), 黑胸大萤叶甲Meristata fraternalis fraternalis (Baly), 黑胸大萤叶甲云南亚种Meristata fraternalis yunnanensis (Laboissiere), 象牙大萤叶甲Meristata pulunini (Bryant), 四带大萤叶甲Meristata quadrifasciata (Hope), 六斑大萤叶甲Meristata sexmaculata (Kollar et Redtenbacher), 黄腹大萤叶甲Meristata spilota (Hope)。亦对Meristata fraternalis yunnanensis 的分类地位进行了探讨,根据其鞘翅斑点及其雄性生殖器形状将原Meristata yunnanensis 降为Meristata fraternalis 的亚种。     

菱角萤叶甲不同地理种群数量性状变异(鞘翅目:叶甲科)

采用模糊聚类、系统聚类和主成分分析的方法对中国12个不同地理种群菱角萤叶甲Galerucella birmanica Jacoby的形态数据进行了分析,探讨了其数量性状变异和地理分布间的关系,并对菱角萤叶甲亚种的分类地位进行了界定。聚类分析将我国菱角萤叶甲12个地理种群分为6个部分:其中西南云贵高原地区的保山种群为一组,华南地区的广州种群为一组,东北地区的沈阳种群为一组,华中地区的孝感种群为一组,长江以北地区的淮安、扬州、泰安和阜阳种群为一组,长江以南地区的常州、嘉兴、青浦和义乌种群为一组,可见不同地理种群菱角萤叶甲的数量性状变异与地理分布之间具有显著的相关性。主成分分析显示,菱角萤叶甲各器官的长度存在相互促进共同变异的关系,变异与性状具有显著正相关性。采用形态学测量的方法对于确定菱角萤叶甲亚种的地位是可行的。     

中国斑蚜科物种多样性及地理分布格局

从分类群的多样性、寄主植物多样性和地理分布多样性3个方面系统研究了中国斑蚜科蚜虫的物种多样性。分类群的多样性从亚科、属和种3个不同阶元进行了描述。寄主植物的多样性体现在：不同蚜虫类群寄主植物的丰富度,其中角斑蚜亚科的寄主最为丰富,包括14个科的植物;同类寄主植物上取食蚜虫的多样性,其中桦木科植物上有15个属的蚜虫取食。在地理分布上,斑蚜科在中国主要分布在古北界的4个区和东洋界的3个区,以古北界的成分占优势;而且华北区种类最为丰富,其次为东北区、华中区、华南区和蒙新区。属的分布类型可分为12种,分别为中国特有分布型、东亚特有分布型、古北界特有分布型、东洋界特有分布型、全北界分布型、全北界和澳洲界共有分布型、古北界和东洋界共有分布型、全北界和东洋界共有分布型、全北界和非洲界共有分布型、古北界、东洋界和非洲界共有分布型、东洋界和澳洲界共有分布型及东洋界、非洲界和澳洲界共有分布型,其中以东亚特有分布型为最丰富,有10个属;其次为全北界分布型,有7个属,同时中国的特有成分也相当高,涉及6个属。纵观整个中国斑蚜科属级阶元的分布类型,中国的斑蚜科以全北界成分为主,其次为东洋界成分。斑蚜科在中国的地理分布,由东向西,种类越来越贫乏,特别是青藏高原,种类很少;从南北向来看,以华北区为中心,向两边扩散,东北区、华南区和华中区种类都有所减少。     

中国伪叶甲科二新属二新种(鞘翅目:伪叶甲科)(英文)

伪叶甲科Lagriidae是鞘翅目的一个小科,全世界已知约2450种。过去有17位外国学者零星地记述了我国该科昆虫22属和124种6变种。1991年以来作者系统地研究了该科的分类、雄性外生殖器形态结构、系统发育和地理分布。本文报道莫伪叶甲属Merklia力和粗伪叶甲属Pachystira二个新属,及两斑莫伪叶甲Merkliabimaculata和凹翅粗伪叶甲Pachystiraimpressipennis二个新种。     

粉条儿菜属(肺筋草科)的地理分布及其物种多样性和分化中心

粉条儿菜属(AletrisL.)隶属于肺筋草科,全世界有23种1变种,东亚有18种1变种,北美东南部有5种,为典型的东亚-北美间断分布的属.本文在种(变种)的水平上,研究了粉条儿菜属的地理分布及其分布中心和多样化中心,并对其起源和分化以及现代洲际间断分布格局的成因进行了分析.结果表明,(1)中国共分布有粉条儿菜属植物15种1变种,而广义的横断山地区集中分布有13种1变种,是东亚粉条儿菜属植物分布最为集中的地区,而且包含该属植物各个进化阶段的代表.因此,广义的横断山地区是粉条儿菜属在东亚的分布中心和多样化中心.(2)根据粉条儿菜属及其近缘属的分布格局推测,该属可能在不晚于第三纪早期,起源于古北大陆.东亚和北美的粉条儿菜属植物形态区别明显,应该是隔离分化的结果.(3)该属植物可能曾经广布于北半球,后来地质、气候以及冰川等因素的变化,导致该属在一些地区灭绝,而仅存于东亚和北美东南部.(4)尽管横断山及其周边地区是东亚粉条儿菜属的多样化中心,但该地区很可能并不是粉条儿菜属最早的分化中心,因横断山地区周边的一些特有种可能是在晚近的时期形成的新特有种;另外,东亚粉条儿菜属一些原始的种类主要分布于我国中东部到日本一带.所以,中国中东部到日本一带可能是粉条儿菜属早期的分化中心.     

淫羊藿属7种植物的雌蕊及果实形态描述的订正

采用了野外观察和光学显微技术对淫羊藿属（Epimedium L.）7种植物的雌蕊及果实的形态结构进行了研究。结果表明：7种植物的心皮数目为1个,胎座类型为边缘胎座,果实类型为蓇葖果。比较了《中国植物志》等文献的记载,订正了文献对7个种＂侧膜胎座＂或＂蒴果＂的记述,并对淫羊藿属的相应特征提出观点。     

丁香属植物的地理分布及其起源演化

木犀科丁香属植物主要分布在中国、朝鲜、日本以及欧洲东南部。中国是丁香属的自然分布中心,丁香主要分布在中国西南、西北、华北、东北等地区。根据植物区系的演化规律,作者认为丁香属起源于中国西南,并以此为中心主要沿中国西南-西北-华北-东北-朝鲜半岛-日本和中国西南-中亚-欧洲的路径散布。近缘种之间存在着遥远的地理隔离,中国原产的华丁香与分布在我国西北及中亚的花叶丁香、欧洲特有种欧洲丁香均为近缘种,表明欧洲丁香的散布与中国西北的种类有着密切的联系。近年分子生物学试验表明羽叶性状是演化中的过渡类型,在研究该属系统演化中具有重要作用。化石记录华北紫丁香在中新世时的华中地区已有存在,说明该属至少在中新世时完成了由西南向华中的演化、辐射。     

The Classification and Distribution of the Genus Calligonum L. in China

The genus Calligonum L. includes a total number of 35 species in the world, of which 24 are in China. They are grouped into four sections, of which Sect. Calliphysae (Fisch. et Mey.) Borszcz. is the most primitive and Sect. Medusae Sosk. et Alexender. is the most progressive. The Calligonum L. is an ancient genus in the arid desert flora, and central Asia is the place of its origin. Some species migrated to the Middle Asia and Iran, developing into a second center there. Also, some newly occurred species of the Middle Asia emigrated eastwards to central Asia, so the genus Calligonum L. in China comprises components of both central Asia and the Middle Asia. The genus Calligonum L. is distributed in North Africa, south Europa and Asia, and China is the eastmost part of the distribution range. They grow in Nei Monggol, Gansu, Qinghai and Xinjiang. There are 12 species in the Zhuengar Basin, covering 50 percent of the total number of species in China, amd thus the genus is the most abundant there.     

中国蔷薇科绣线菊亚科的演化、分布——兼述世界绣线菊亚科植物的分布

绣线菊亚科是蔷薇科最原始的亚科,共有22属260余种, 包括常绿和落叶两大类群,前者是 原始类型。我国有8属100种,全都为落叶性。本文着重讨论中国各属的起源、演化和分布等 ,同时也概述全亚科植物在世界各植物区的分布等问题。绣线菊属Spiraea是该亚科落叶类群中最原始的属,它在早期发生趋异进化,衍生出形态各异而亲缘关系密切 的不同属,本文阐明了中国各属的系统位置和属间的亲缘关系。通过对我国各属地理分布的 分析对比,属的分布区可归纳为5个类型。对全球绣线菊亚科植物在世界各植物区中的属、种数统计表明,东亚区有8属105种,其中有96个特有种,是该亚科植物分布最多而又最集中 地区,具有在系统发育上处于各主要演化阶段的落叶类型,因此,东亚区是全球绣线菊亚科植 物的现代分布和分化中心,也是落叶类群发生和发展的关键地区。在北美洲,从马德雷区至落基山区一带分布着11属46种,均为特有种,显然北美洲西部也是该亚科植物的现代分布中心,但可能是第二分布中心。南美洲至今保存2个较古老的常绿属,即Quillaja和K ageneckia,基于此,南美洲可能是绣线菊亚科某些常绿属早期分化和发展的关键地区 。中国绣线菊亚科植物在东亚区占绝对优势,有8属82种,其中有62个特有种,分别占该区属 、种和 特有种数的100%、82%、和65%, 这些类群分布最密集地区是在中国喜马拉雅森林植物亚区 中的横断山脉地区和中国日本森林植物亚区的西部,这一带是中国绣线菊亚科的现代分布和多样性中心,很可能是某些属的发源地。由此看来,绣线菊亚科的落叶属可能起源于劳亚古陆。据化石记载,该亚科植物的起源时间可以追溯到白垩纪早白垩世。     

The Evolution and Distribution of Subfam. Spiraeoideae (Rosaceae) of China,with Special Reference to Distribution of the Subfamily in the World

The subfam. Spiraeoideae, consisting of 22 genera and more than 260 species in the world,is the most primitive subfamily of Rosaceae. It has developed into two groups,i.e. evergreen and deciduous ones, of which eight genera and 100 species in China are totally deciduous. In the present paper, the origin,evolution and distribution of the Chinese genera is discussed mainly, and the distribution of the whole subfamily in the floristic regions of the world is also mentioned. Based on evolutionary trends of morphological characters, Spiraea L. is considered as the most primitive genus in the deciduous group of subfam. Spiraeoideae, from which some genera are been derived, the systematic position and evolutionary relationships between different genera are elucidated in this paper. Through the analysis on the geographical distribution of the genera in China, the areal types may be divided as follows: (1) North Temperate Type: Spiraea, Physocarpus, Aruncus. (2) East Asian and North American Disjunct Type: Sorbaria. (3) Mediterranean, West Asian (or Central Asia) and East Asian Type: Sibiraea. (4) Temperate Asian Type: Exochorda.(5) East Asian Type: (a) Sino Himalayan Distribution: Neillia; (b) Sino Japan Distribution: Stephanandra. After analysis of the distribution of subfam. Spiraeoideae in the world, it is shown that the Eastern Asiatic Region, being the richest in genera, species and endemic species of the world,is not only the center of distribution and differentiation,but also an important region for occurrence and development of some deciduous genera of this subfamily, while in North America, the Madrean Region and Rocky Mountain Region, genera, species and endemic species are abundant, which indicates that the western part of North America is also the distribution center of this subfamily at the present, but it may be the secondary center of distribution. It can be seen that the relatively primitive and evergreen g enera, i.e. Quillaja and Kageneckia, are now confined to South America. The fact implies that the South America may be the region for early differentiation and development of the evergreen genera in Subfam. Spiraeoideae. The analysis of Chinese plants has shown that China has the most members of the subfamily in Eastern Asiatic Region, with eight genera, 82 species and 62 endemic species and that the maximum concentration is in western Sichuan, northwestern Yunnan and their adjacent areas. It is very obvious that the center of distribution and diversity of Subfam. Spiraeoideae in China lies in the Hengduan Mountain Region of Sino Himalayan Forest Subkingdom and the western part of Sino Japan Forest Subkingdom, where may be the birthplace of some genera in China. It may be considered that the deciduous genera of Subfam. Spiraeoideae might have originated in Laurasia.According to the fossil records, the time of origin of Subfam.Spiraeoideae dates back to the Lower Cretaceous.     

On the geographical distribution of the Juglandaceae

The present paper aims to discuss the geog raphical distribution of the Juglandaceae on the basis of unity of the phylogeny and the process of dispersal in the plants. The paper is divided into the following three parts: 1. The systematic positions and the distribution patterns of nine living genera in the family Juglandaceae (namely, Engelhardia, Oreomunnea, Alfaroa, Pterocarya, Cyclocarya, Juglans, Carya, Annamocarya and Platycarya) are briefly discussed. The evolutional relationships between the different genera of the Juglandaceae are elucidated. The fossil distribution and the geological date of the plant groups are reviewed. Through the analysis for the geographical distribution of the Juglandaceous genera, the distribution patterns may be divided as follows: A. The tropical distribution pattern a. The genera of tropical Asia distribution: Engelhardia, Annamocarya. b. The genera of tropical Central America distribution: Oreomunnea, Alfaroa. B. The temperate distribution pattern c. The genus of disjunct distribution between Western Asia and Eastern Asia: Pterocarya. d. The genus of disjunct distribution between Eurasia and America: Juglans. e. The genus of disjunct distribution between Eastern Asia and North America: Carya. f. The genera whose distribution is confined to Eastern Asia: Cyclocarya, Platycarya. 2. The distribution of species According to Takhtajan’s view point of phytochoria, the number of species in every region are counted. It has shown clearily that the Eastern Asian Region and the Cotinental South-east Asian Region are most abundant in number of genera and species. Of the 71 living species, 53 are regional endemic elements, namely 74.6% of the total species. The author is of the opinion that most endemic species in Eurasia are of old endemic nature and in America of new endimic nature. There are now 7 genera and 28 species in China, whose south-western and central parts are most abundant in species, with Province Yunnan being richest in genera and species. 3. Discussions of the distribution patterns of the Juglandaceae A. The centre of floristic region B. The centre of floristic regions is determined by the following two principles: a. A large number of species concentrate in a district, namely the centre of the majority; b. Species of a district can reflect the main stages of the systematic evolution of the Juglandaceae, namely the centre of diversity. It has shown clearly that the southern part of Eastern Asian region and the northern part of Continental South-east Asian Region (i.c. Southern China and Northern Indo-China) are the main distribution centre of the Juglandaceae, while the southern part of Sonora Region and Caribbean Region (i.c. South-western U.S.A., Mexico and Central America) are the secondary distribution centre. As far as fossil records goes, it has shown that in Tertiary period the Juglandaceae were widely distributed in northern Eurasia and North America, growing not only in Europe and the Caucasus but also as far as in Greenland and Alaska. It may be considered that the Juglandaceae might be originated from Laurasia. According to the analysis of distribution pattern for living primitive genus, for example, Engelhardia, South-western China and Northern Indo-China may be the birthplace of the most primitive Juglandaceous plants. It also can be seen that the primitive genera and the primitive sections of every genus in the Juglandaceae have mostly distributed in the tropics or subtropics. At the same time, according to the analysis of morphological characters, such as naked buds in the primitive taxa of this family, it is considered that this character has relationship with the living conditions of their ancestors. All the evidence seems to show that the Juglandaceae are of forest origin in the tropical mountains having seasonal drying period. B. The time of the origin The geological times of fossil records are analyzed. It is concluded that the origin of the Juglandaceae dates back at least as early as the Cretaceous period. C. The routes of despersal After the emergence of the Juglandaceous plant on earth, it had first developed and dispersed in Southern China and Indo-China. Under conditions of the stable temperature and humidity in North Hemisphere during the period of its origin and development, the Juglandaceous plants had rapidly developed and distributed in Eurasia and dispersed to North America by two routes: Europe-Greenland-North America route and Asia-Bering Land-bridge-North America route. From Central America it later reached South America. D. The formaation of the modern distribution pattern and reasons for this formation. According to the fossil records, the formation of two disjunct areas was not due to the origin of synchronous development, nor to the parallel evolution in the two continents of Eurasia and America, nor can it be interpreted as due to result of transmissive function. The modern distribution pattern has developed as a result of the tectonic movement and of the climatic change after the Tertiary period. Because of the continental drift, the Eurasian Continent was separated from the North American Continent, it had formed a disjunction between Eurasia and North America. Especially, under the glaciation during the Late Tertiary and Quaternary Periods, the continents in Eurasia and North America were covered by ice sheet with the exception of “plant refuges”, most plants in the area were destroyed, but the southern part of Eastern Asia remained practically intact and most of the plants including the Juglandaceae were preserved from destruction by ice and thence became a main centre of survival in the North Hemisphere, likewise, there is another centre of survival in the same latitude in North America and Central America. E. Finally, the probable evolutionary relationships of the genera of the Juglanda-ceae is presented by the dendrogram in the text.     

影响入侵种反枝苋分布的环境因子分析及可能分布区预测

反枝苋(Amaranthus retroflexus)是苋属入侵种中发生频率最多、分布最广、危害最严重的杂草。基于反枝苋在世界范围内4 207个实际分布点及其对应的气候、地形和土壤3类要素28个环境因子的定量关系,利用主成分分析确定了影响其分布的主要环境因子,据此估测其中心可能分布区和最大可能分布区,并与实际分布点进行比较。结果表明:14个环境因子在决定反枝苋全球分布格局中起着重要作用。反枝苋中心分布区位于新西兰南部、澳大利亚东南部、南美洲北部少数地区、北美洲西北部及东南部部分地区、欧洲大部分地区和中国东南部,最大可能分布区位于南美洲中南部、北美洲大部分、非洲北部小部分、澳大利亚南部及北部少数区域、欧洲大部分地区和亚洲大部分地区及中国除西藏、青海、新疆、四川西部以外的地区。中心分布区的预测结果与实际分布点吻合较好,而最大分布区则过于广阔。