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     

中国新桦斑蚜属分类研究(同翅目:蚜科:角斑蚜亚科)

研究了中国蚜科Aphididae角斑蚜亚科Myzocallidinae1新纪录属,即新桦斑蚜属Neobetulaphis Basu,1964。中国分布3种,其中包括2新纪录种,白新桦斑蚜N.alba Higuchi,1972和裸新桦斑蚜N.pusilla Basu,1964。每种提供了观察标本,地理分布,寄主植物等信息;新纪录种还提供了较详细的形态和形态特征图。研究标本保存在中国科学院动物研究所动物标本馆。     

中国侧棘斑蚜属分亚属研究及五新纪录亚属(同翅目:蚜科:角斑蚜亚科)

研究认为中国侧棘斑蚜属Tuberculatus Mordvilko,1894蚜虫有7个亚属,刺棘斑蚜亚属Acanthocallis Matsumura 1917,东方棘斑蚜亚属Orientuberculoides Hille Ris Lambers,1974,针棘斑蚜亚属Acanthotuberculatus Quednau,1999,阿棘斑蚜亚属Arakawana Matsumura ,1917,日本棘斑蚜亚属Nippocallis Matsumura,1917,中日棘斑蚜亚属Nippotuberculatus Quednan,1999和肖棘斑蚜亚属Tuberculoides van der Goot,1915。给出分亚属检索素,并记述5个中国新纪录亚属和一个新纪录种环肖棘斑蚜Tuberculatus(Tuhberculoides)annulatus(Hartig 1841),研究标本存放在中国科学院动物所动物标本馆。     

中国扁叶甲属地理分布格局研究(叶甲科,叶甲亚科)

本文运用GIS技术研究扁叶甲属Gastrolina在中国的地理分布格局。以采集地的行政单元转换地理坐标与动物地理区划图叠加后产生叶甲的地理分布图。结果显示此属主要分布在华中区、华北区、华南区、西南区、东北区。根据地理分布图及有关分析,认为华中区中部、华北区西北部是该属的丰富度中心和分布中心,华中区中部为中国扁叶甲多样性中心和分化中心。     

中国椴斑蚜属研究(同翅目,蚜科,角斑蚜亚科)

中国椴斑蚜属Tiliaphis Takahashi已知2种,朝鲜椴斑蚜Tiliaphis coreanus Quednau,1979和小椴斑蚜T.shinae(Shinji,1924)(中国新纪录)。文中提供了分种检索表,各种提供了观察标本、地理分布、寄主植物等信息新纪录种提供了详细的形态记述和形态特征图。研究标本保存在中国科学院动物研究所动物标本馆。     

中国刻斑蚜属分类研究(同翅目: 蚜科: 角斑蚜亚科)

研究了中国蚜科Aphididae角斑蚜亚科Myzocallidinae的刻斑蚜属 Clethrobius Mordvilko,1928,记述了中国2新纪录种,毛刻斑蚜 C.comes(Walker,1848)和赤杨刻斑蚜C.dryobius Chakrabarti et Raychaudhuri,1976,编制了中国刻斑蚜属分种检索表,各种提供了寄主植物、分布及形态特征图。研究标本保存在中国科学院动物研究所动物标本馆。     

中国长斑蚜属研究及新种记述(同翅目：斑蚜科)

该文系统研究了中国长斑蚜属Tinocallis Matsumura的15种蚜虫,其中包括:1个新种,短节长斑蚜T. microtylodes sp.nov.和2个中国新记录种,斑长斑蚜T.platani(Kaltenbach,1943)和木兰长斑蚜T. magnoliae Ghosh & Raychaudhuri,1972。同时提供了该属中国分布种类的检索表,每种提供有详细的寄主植物和地理分布资料,新种还提供了重要的形态特征图。所有标本包括模式标本均保存在中国科学院动物研究所。     

中国新纪录属--长角斑蚜属研究(同翅目:蚜科:角斑蚜亚科)

研究了中国蚜科Aphididae角斑蚜亚科Calaphidinae 1新纪录属－长角斑蚜属Calaphis Walsh,1863,记述2新纪录种,居桦长角斑蚜Calaphis betulicola(Kaltenbach,1843)和相似长角斑蚜Calaphis similis Quednau,1979。编制中国长角斑蚜属分种检索表,每种提供形态记述、寄主植物、分布及形态特征图。研究标本保存在中国科学院动物研究所动物标本馆。     

中国新纪录属--斑大蚜属研究(同翅目,蚜科,大蚜亚科)

研究了中国蚜科Aphididae大蚜亚科Lachninae 1新纪录属,斑大蚜属Maculolach us Gaumont,1920,记述模式种蔷薇斑大蚜Maculolachnus submacula(Walker,1848).提供了形态描述、寄主植物、分布及形态特征图.研究标本保存在中国科学院动物研究所动物标本馆.     

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.     

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。     

Studies on Geographical Distribution Pattern of the Subgenus Pogonophace (Fabaceae: Astragalus) in China Using GIS Technique

The geographical distribution maps of the subgenus Pogonophace (Fabaceae: Astragalus) in China were designed and drawn using GIS cartographic technique. The species of the subgenus and county of China were treated as the basic composition units in the GIS cartographic technique. Most of the distribution maps were shown in spots. The distribution pattern of the subgenus illustrates that it is a peculiar group to adapt the cold alpine environment and distribute mainly in Hengduan Mountains and Himalayas. According to the geographical distribution maps and some statistic analyses, Hengduan Mountains region is suggested to be the distribution center, differentiation center and endemic center of the subgenus. Some vicariance traces at levels of the species or sections are very interesting among the distribution patterns of the subgenus and shown clearly in the maps.     

用GIS技术研究中国簇毛黄耆亚属（豆科：黄耆属）的地理分布式样

用ＧＩＳ技术设计和绘制了豆科黄耆属（Ａｓｔｒａｇａｌｕｓ Ｌ．）簇毛黄耆亚属在中中的地理分布图。以种类和县级分面为基本构图单元。分布图形均呈斑块状。分布式样提示出亚属是一个集中分布在横断山和喜马拉雅,适应于高寒山地的特化类群。根据地理公布直观图及有关统计分析,认为横断山是这个亚属的分布中心、分化中心和特有中心。公布式样和直观图还揭示出一些种之间、组之间有趣的替代现象。     

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。     

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。     

鹅观草属的几个新组合

本文报道了禾本科鹅观草属的三个种级新组合和四个变种级新组合。即大丛鹅观草Roegneria magnicaespis (D.F.Cui)L.B.Cai;新疆鹅观草Roegneria sinkiangensis(D.F.Cui)L.B.Cai;阿尔泰鹅观草Roegneria altaica(D.F.Cui)L.B.Cai;短芒鹅观草Roegneria glaberrima var.breviarista (D.F.Cui)L.B.Cai;林缘鹅观草Roegneria mutabilis var.nemoralis (D.F.Cui)L.B.Cai;多花鹅观草Roegneria abolinii var.pluriflora (D.F.Cui)L.B.Cai和曲芒鹅观草Roegneria tschimganica var.glabrispicula (D.F.Cui)L.B.Cai。