Major evolutionary events in the origin and diversification of the fern genus Polystichum (Dryopteridaceae)

Recent advances in molecular systematics of the ferns make it possible to address long-standing questions about classification of the major fern genera, such as the worldwide genus Polystichum (Dryopteridaceae), comprising at least 200 species. In this study we examined rbcL sequences and morphological characters from 55 fern taxa: 34 were from Polystichum and 21 were from other genera in the Dryopteridaceae. We found that Phanerophlebia, possibly including Polystichopsis, is the sister group to Polystichum sensu lato (s.l.), including Cyrtomium. Polystichum as commonly recognized is paraphyletic. Our results lead us to suggest recognizing the clade of earliest diverging Polystichum species as a distinct genus (Cyrtomidictyum) and to continue to recognize Cyrtomium as a separate genus, leaving a monophyletic Polystichum sensu stricto (s.s.). We resolved a tropical American clade and an African clade within Polystichum s.s. However, the resemblance between the once-pinnate, bulb-bearing calciphilic species found in Asia and the West Indies appears to be the result of convergent evolution. Optimizing our morphological character transformations onto the combined phylogeny suggests that the common ancestor of Polystichum s.l. and Phanerophlebia had evolved the common features of the alliance, including ciliate petiole-base scales, once-pinnate fronds, ultimate segments with scarious tips, peltate indusia, and microscales.     

Molecular phylogeny and biogeography of the endemic Hawaiian Succineidae (Gastropoda: Pulmonata)

The endemic Hawaiian Succineidae represent an important component of the exceptionally diverse land snail fauna of the Hawaiian Islands, yet they remain largely unstudied. We employed 663-bp fragments of the cytochrome oxidase I (COI) mitochondrial gene to investigate the evolution and biogeography of 13 Hawaiian succineid land snail species, six succineid species from other Pacific islands and Japan, and various outgroup taxa. Results suggest that: (1) species from the island of Hawaii are paraphyletic with species from Tahiti, and this clade may have had a Japanese (or eastern Asian) origin; (2) species from five of the remaining main Hawaiian islands form a monophyletic group, and the progression rule, which states that species from older islands are basal to those from younger islands, is partially supported; no geographic origin could be inferred for this clade; (3) succineids from Samoa are basal to all other succineids sampled (maximum likelihood) or unresolved with respect to the other succineid clades (maximum parsimony); (4) the genera Succinea and Catinella are polyphyletic. These results, while preliminary, represent the first attempt to reconstruct the phylogenetic pattern for this important component of the endemic Hawaiian fauna.     

Molecular insights into the phylogenetic structure of the spider genus Theridion (Araneae, Theridiidae) and the origin of the Hawaiian Theridion-like fauna

The Hawaiian happy face spider ( Theridion grallator Simon, 1900), named for a remarkable abdominal colour pattern resembling a smiling face, has served as a model organism for understanding the generation of genetic diversity. Theridion grallator is one of 11 endemic Hawaiian species of the genus reported to date. Asserting the origin of island endemics informs on the evolutionary context of diversification, and how diversity has arisen on the islands. Studies on the genus Theridion in Hawaii, as elsewhere, have long been hampered by its large size (> 600 species) and poor definition. Here we report results of phylogenetic analyses based on DNA sequences of five genes conducted on five diverse species of Hawaiian Theridion , along with the most intensive sampling of Theridiinae analysed to date. Results indicate that the Hawaiian Islands were colonised by two independent Theridiinae lineages, one of which originated in the Americas. Both lineages have undergone local diversification in the archipelago and have convergently evolved similar bizarre morphs. Our findings confirm para- or polyphyletic status of the largest Theridiinae genera: Theridion , Achaearanea and Chrysso . Convergent simplification of the palpal organ has occurred in the Hawaiian Islands and in two continental lineages. The results confirm the convergent evolution of social behaviour and web structure, both already documented within the Theridiidae. Greater understanding of phylogenetic relationships within the Theridiinae is key to understanding of behavioural and morphological evolution in this highly diverse group.     

The microsoroid ferns: Inferring the relationships of a highly diverse lineage of Paleotropical epiphytic ferns (Polypodiaceae, Polypodiopsida)

The relationships of the microsoroid ferns were studied using a DNA sequence-based phylogenetic approach. Nucleotide sequences for up to four chloroplast genome regions were assembled for 107 samples from 87 species. Microsoroids s.l. include six lineages of which two are species rich. The results indicate that several genera are not monophyletic (e.g. Microsorum), several controversial genera are confirmed to be monophyletic (e.g. Leptochilus), and some genera new to science should be recognized (M. membranaceum clade). Unique insights were gained into the biogeographic history of this highly diverse epiphytic vascular plant lineage that is widespread in continental Asia to Australasia. Evidence was found for splits into lineages diversifying in parallel in continental Asia and Malesia. No evidence was recovered for an African radiation because all African microsoroid species either also are found in Asia or have sister species in continental Asia. In contrast, evidence for independent radiations were discovered for the Australasian region.     

Evolution of Cyrtandra (Gesneriaceae) in the Pacific Ocean: the origin of a supertramp clade

Cyrtandra comprises at least 600 species distributed throughout Malesia, where it is known for many local endemics and in Polynesia and Micronesia, where it is present on most island groups, and is among the most successfully dispersing genera of the Pacific. To ascertain the origin of the oceanic Pacific island species of Cyrtandra, we sequenced the internal transcribed spacers of nuclear ribosomal DNA of samples from throughout its geographical range. Because all oceanic Pacific island species form a well-supported clade, these species apparently result from a single initial colonization into the Pacific, possibly by a species from the eastern rim of SE Asia via a NW-to-SE stepping stone migration. Hawaiian species form a monophyletic group, probably as a result of a single colonization. The Pacific island clade of Cyrtandra dispersed across huge distances, in contrast to the apparent localization of the SE Asian clades. Although highly vagile, the Pacific clade is restricted to oceanic islands. Individual species are often endemic to a single island, characteristic of the "supertramp" life form sensu Diamond (1974, Science 184: 803-806). The evolution of fleshy fruit within Cyrtandra provided an adaptation for colonization throughout the oceanic Pacific via bird dispersal from a single common ancestor.     

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.     

Molecular phylogenetics of the moth genus Omiodes Guenée (Crambidae: Spilomelinae), and the origins of the Hawaiian lineage

The moth genus Omiodes (Crambidae) comprises about 80 species and has a circumtropical distribution, with the type species, O. humeralis, occurring in Central America. In Hawaii, there are 23 native species currently placed in Omiodes, but this classification has been disputed, and they were previously placed in various other genera. We used molecular phylogenetic analyses to assess the monophyly of Omiodes as a whole, and specifically of the Hawaiian species, as well as their geographic origins and possible ancestral host plants. Mitochondrial (COI) and nuclear (wingless, EF1α, CAD, and RPS5) DNA was sequenced for Omiodes from Hawaii, South America, and Australasia, along with many other putative outgroup spilomeline genera. Phylogenies were estimated using maximum likelihood and Bayesian inference, and various taxon and character datasets. With the exception of two paleotropical species (O. basalticalis and O. odontosticta, whose placement was unresolved) all Hawaiian, paleotropical and neotropical Omiodes, including the type species, fell within a well-supported, monophyletic clade. Although the center of diversity for Omiodes is in the Neotropics, its center of origin was ambiguous, due to poor resolution of the basal splits between paleotropical and neotropical Omiodes. Very low genetic divergence within the Hawaiian Omiodes suggests a relatively recent colonization of the Hawaiian Islands. Phylogenies constructed using all codon positions were poorly resolved at intergeneric levels, and did not reveal a sister taxon for Omiodes, but phylogenies constructed using only first and second codon positions suggested a close relationship with Cnaphalocrocis. The monophyly of several other spilomeline genera is also discussed.     

Phylogenetic relationships in the cricket tribe Xenogryllini (Orthoptera,Gryllidae, Eneopterinae) and description of the Indian genus Indigryllus gen. nov.

The subfamily Eneopterinae is known greatly for its diversified acoustic modalities and disjunct distribution. Within Eneopterinae, tribe Lebinthini is the most studied group, due to its highest species diversity (ca. 150 species in 12 genera), endemic distribution on the islands of Southeast Asia and of the South West Pacific, males’ ability to produce high‐frequency calling songs, and evolution of females’ vibrational response. To investigate the distribution pattern and diversification of acoustic and behavioral attributes in a larger frame, clear understanding of phylogenetic relationships within other tribes of Eneopterinae is vital. In this study, we focus on the tribe Xenogryllini, sister group of Lebinthini. Xenogryllini, as opposed to Lebinthini, is known by fewer species (11 species in two genera), distributed widely in continental Asia and Africa, and for producing low‐frequency calling songs. We describe a new genus Indigryllus with a new species of the tribe Xenogryllini, discovered from the southwest of India. We used eight molecular genetic markers to reconstruct the phylogenetic relationships. The resultant phylogenetic tree is used to compare and discuss distribution patterns and acoustic modalities between Lebinthini and Xenogryllini.     

Feral Cat Globetrotters: genetic traces of historical human‐mediated dispersal

Endemic species on islands are highly susceptible to local extinction, in particular if they are exposed to invasive species. Invasive predators, such as feral cats, have been introduced to islands around the world, causing major losses in local biodiversity. In order to control and manage invasive species successfully, information about source populations and level of gene flow is essential. Here, we investigate the origin of feral cats of Hawaiian and Australian islands to verify their European ancestry and a potential pattern of isolation by distance. We analyzed the genetic structure and diversity of feral cats from eleven islands as well as samples from Malaysia and Europe using mitochondrial DNA (ND5 and ND6 regions) and microsatellite DNA data. Our results suggest an overall European origin of Hawaiian cats with no pattern of isolation by distance between Australian, Malaysian, and Hawaiian populations. Instead, we found low levels of genetic differentiation between samples from Tasman Island, Lana'i, Kaho'olawe, Cocos (Keeling) Island, and Asia. As these populations are separated by up to 10,000 kilometers, we assume an extensive passive dispersal event along global maritime trade routes in the beginning of the 19th century, connecting Australian, Asian, and Hawaiian islands. Thus, islands populations, which are characterized by low levels of current gene flow, represent valuable sources of information on historical, human‐mediated global dispersal patterns of feral cats.     

鳞毛蕨科的孢子形态研究

对鳞毛蕨科及其相近类群的19属65种的孢子形态进行了光学显微镜观察,并对其中12属30种进行了扫描电镜观察。鳞毛蕨科的孢子左右对称,极面观为椭圆形、近球形,赤道观为肾形,极轴/赤道轴的比值为0.60～0.86;单缝孢,裂缝长度约为孢子全长的1/2～3/4,属中至大型孢子。鳞毛蕨科具有多样性的外壁纹饰:不仅包括刺状、瘤状、颗粒状、脊状、窗孔状、耳状、片状及翅状等几种基本类型,而且还存在一些中间过渡类型。根据孢子形态特征,对本科的属间关系进行了探讨。孢子形态特征的相似性支持假复叶耳蕨属、肉刺蕨属、球盖蕨科与鳞毛蕨属的近缘关系,黔蕨属与复叶耳蕨属间的近缘关系。玉龙蕨属的两个种的孢子纹饰与耳蕨属的部分种一致,支持将玉龙蕨属作为耳蕨属的异名处理。拟贯众属独特的翅状纹饰支持将其从鳞毛蕨科中分离出去。     

根据叶绿体ndhF和核核糖体DNA序列推断梓属(紫葳科)的系统发育

Phylogenetics of Chilopsis and Catalpa (Bignoniaceae) was elucidated based on sequences of chloroplast ndhF and the nrDNA ITS region. In Bignoniaceae, Chilopsis and Catalpa are most closely related as sister genera. Our data supported section Macrocatalpa of the West Indies and section Catalpa of eastern Asian and North American continents. Within section Catalpa, Catalpa ovata of eastern Asia form a clade with North American species, C. speciosa and C. bignonioides, while the other eastern Asian species comprise a clade where C. duclouxii is sister to the clade of C. bungei and C. fargesii. The Caribbean species of Catalpa diverged early from the continental species. More studies are needed to test whether the phylogenetic pattern is common in eastern Asian-North American disjunct genera with species in the West Indies.     

Origin,Differentiation, and Geographic Distribution of the Chenopodiaceae

Numbers of species and genera,endemic genera,extant primitive genera,relationship and distribution patterns of presently living Chenopodiaceae(two subfamilies,12 tribes,and 118 genera)are analyzed and compared for eight distributional areas,namely central Asia,Europe,the Mediterranean region,Africa,North America,South America, Australia and East Asia． The Central Asia,where the number of genera and diversity of taxa are greater than in other areas,appears to be the center of distribution of extant Chenopodiaceae．North America and Australia are two secondary centers of distribution． Eurasia has 11 tribes out of the 12,a total of 70 genera of extant chenopodiaceous plants,and it contains the most primitive genera of every tribe． Archiatriplex of Atripliceae,Hablitzia of Hablitzeae,Corispermum of Corispermeae,Camphorosma of Camphorosmaea,Kalidium of Salicornieae,Polecnemum of Polycnemeae,Alexandra of Suaedeae,and Nanophyton of Salsoleae,are all found in Eurasia,The Beteae is an Eurasian endemic tribe,demonstrating the antiquity of the Chenopodiaceae flora of Eurasia．Hence,Eurasia is likely the place of origin of chenopodiaceous plants． The presence of chenopodiaceous plants is correlated with an arid climate．During the Cretaceous Period,most places of the continent of Eurasia were occupied by the ancient precursor to the Mediterranean,the Tethys Sea．At that time the area of the Tethys Sea had a dry and warm climate．Therefore,primitive Chenopodiaceae were likely present on the beaches of this ancient land．This arid climatic condition resulted in differentiation of the tribes Chenopodieae,Atripliceae,Comphorosmeae,Salicornieae,etc．,the main primitive tribes of the subfamily Cyclolobeae. Then following continental drift and the Laurasian and Gondwanan disintegration, the Chenopodiaceae were brought to every continent to propagate and develop, and experience the vicissitudes of climates, forming the main characteristics and distribution patterns of recent continental floras. The tribes Atripliceae, Chenopodieae, Camphorosmeae, and Salicornieae of recent Chenopodiaceae in Eurasia, North America, South America, southern Africa, and Australia all became strongly differentiated. However, Australia and South America, have no genera of Spirolobeae except for a few maritime Suaeda species. The Salsoleae and Suaedeae have not arrived in Australia and South America, which indicates that the subfamily Spirolobeae developed in Eurasia after Australia separated from the ancient South America-Africa continent, and South America had left Africa. The endemic tribe of North America, the tribe Sarcobateae, has a origin different from the tribes Salsoleae and Suaedeae of the subfamily Spirolobeae. Sarcobateae flowers diverged into unisexuality and absence of bractlets. Clearly they originated in North America after North America had left the Eurasian continent. North America and southern Africa have a few species of Salsola, but none of them have become very much differentiated or developed, so they must have arrived through overland migration across ancient continental connections. India has no southern African Chenopodiaceae floristic components except for a few maritime taxa, which shows that when the Indian subcontinent left Africa in the Triassic period, the Chenopodiaceae had not yet developed in Africa. Therefore, the early Cretaceous Period about 120 million years ago, when the ancient Gondwanan and Laurasian continents disintegrated, could have been the time of origin of Chenopodiaceae plants.The Chinese flora of Chenopodiaceae is a part of Chenopodiaceae flora of central Asia. Cornulaca alaschnica was discovered from Gansu, China, showing that the Chinese Chenopodiaceae flora certainly has contact with the Mediterranean Chenopodiaceae flora. The contact of southeastern China with the Australia Chenopodiaceae flora, however, is very weak.     

Hawaiian biogeography and the islands' freshwater fish fauna

Aim This paper describes known patterns in the distributions and relationships of Hawaiian freshwater fishes, and compares these patterns with those exhibited by Hawaii's terrestrial biota. Location The study is based in Hawaii, and seeks patterns across the tropical and subtropical Indo‐west Pacific. Methods The study is based primarily on literature analysis. Results The Hawaiian freshwater fish fauna comprises five species of goby in five different genera (Gobiidae). Four species are Hawaiian endemics, the fifth shared with islands in the western tropical Pacific Ocean. All genera are represented widely across the Indo‐west Pacific. All five species are present on all of the major Hawaiian islands. All five species are amphidromous – their larval and early juvenile life being spent in the sea. Although there has been some local phyletic evolution to produce Hawaiian endemics, there has been no local radiation to produce single‐island endemics across the archipelago. Nor is there evidence for genetic structuring among populations in the various islands. Main conclusions In this regard, the freshwater fish fauna of Hawaii differs from the well‐known patterns of local evolution and radiation in Hawaiian Island terrestrial taxa. Amphidromy probably explains the biogeographical idiosyncrasies of the fish fauna – dispersal through the sea initially brought the fish species to Hawaii, and gene flow among populations, across the archipelago, has hitherto inhibited the evolution of local island endemics, apparently even retarding genetic structuring on individual islands.     

藜科植物的起源、分化和地理分布

全球藜科植物共约130属1500余种,广泛分布于欧亚大陆、南北美洲、非洲和大洋洲的半干旱及盐碱地区。它基本上是一个温带科,对亚热带和寒温带也有一定的适应性。本文分析了该科包含的1l族的系统位置和分布式样,以及各个属的分布区,提出中亚区是现存藜科植物的分布中心,原始的藜科植物在古地中海的东岸即华夏陆台(或中国的西南部)发生,然后向干旱的古地中海沿岸迁移、分化,产生了环胚亚科主要族的原始类群;起源的时间可能在白垩纪初,冈瓦纳古陆和劳亚古陆进一步解体的时期。文章对其迁移途径及现代分布式样形成的原因进行了讨论。     

Biogeographic mirages? Molecular evidence for dispersal‐driven evolution in Hydrobiusini water scavenger beetles

Water beetles of the tribe Hydrobiusini are globally distributed in the northern hemisphere and all austral continents except Antarctica. A remarkable clade also occurs in the Hawaiian Islands. The phylogenetic relationships among genera were recently investigated using a combination of molecules and morphology. Here, we use this phylogenetic framework to address the biogeographic evolution of this group using Bayesian fossil‐based divergence times, and model‐based maximum likelihood ancestral range estimations. We recover an origin of the tribe in the Cretaceous ca. 100 Ma. Our biogeographic analyses support an origin of the tribe in Laurasia followed by the colonization of Australia. However, a Gondwanan origin of the group cannot be ruled out when considering the fossil record. The timeframe of the tribe's evolution as well as the model‐based approach of ancestral range estimation favour a scenario invoking multiple transoceanic dispersal events over a Gondwana vicariance hypothesis. The Hawaiian radiation originated from long‐distance dispersal to now‐submerged islands, paired with dispersal to new islands as they formed.     

峨眉山蕨类植物区系的初步研究

依据2004~2006年的野外调查和标本馆标本以及文献资料,初步分析了峨眉山蕨类植物区系的地理特征,结果表明:峨眉山共有蕨类植物46科110属425种,优势科为蹄盖蕨科、水龙骨科和鳞毛蕨科,共192种,占总种数45.2%,优势属为耳蕨属、鳞毛蕨属、凤尾蕨属和蹄盖蕨属等;在科、属的水平上,为热带分布型,以泛热带分布为主,而种的地理分布则以温带分布的中国特有和东亚成分占绝对优势,分别为36.5%和32.0%,揭示了峨眉山蕨类植物区系是以温带性质为主的亚热带类型,具有较强的热带亲缘;与大巴山关系密切,和云南哀牢山有一定的联系,而与秦岭、西藏和陕西天华山的关系较为疏远。     

Phylogenetic position and biogeography of Hillebrandia sandwicensis (Begoniaceae): a rare Hawaiian relict

The Begoniaceae consist of two genera, Begonia, with approximately 1400 species that are widely distributed in the tropics, and Hillebrandia, with one species that is endemic to the Hawaiian Islands and the only member of the family native to those islands. To help explain the history of Hillebrandia on the Hawaiian Archipelago, phylogenetic relationships of the Begoniaceae and the Cucurbitales were inferred using sequence data from 18S, rbcL, and ITS, and the minimal age of both Begonia and the Begoniaceae were indirectly estimated. The analyses strongly support the placement of Hillebrandia as the sister group to the rest of the Begoniaceae and indicate that the Hillebrandia lineage is at least 51-65 million years old, an age that predates the current Hawaiian Islands by about 20 million years. Evidence that Hillebrandia sandwicensis has survived on the Hawaiian Archipelago by island hopping from older, now denuded islands to younger, more mountainous islands is presented. Various scenarios for the origin of ancestor to Hillebrandia are considered. The geographic origin of source populations unfortunately remains obscure; however, we suggest a boreotropic or a Malesian-Pacific origin is most likely. Hillebrandia represents the first example in the well-studied Hawaiian flora of a relict genus.     

The Geographical Distribution of the Subfamily Cyrtandroideae Endl. Emend. Burtt (Gesneriaceae)

Based on Burtts classification and relevant references, the geographical distribution of the subfamily Cyrtandroideae Endl. emend. Burtt is outlined, distribution maps of 79 genera are provided, and some evolutionary trends of the taxa are inferred. The main points may be summarized as follows:1. The centre of distribution The Cyrtandroideae consists of four tribes, 79 genera and about 1770 species, widely distributed in tropical and subtropical regions of the Old World, ranging from Guinea eastwards to Nukuhiva Islands and from Western Bulgaria southwards to Southern Natal, with only one species disjunctly occurring in tropical America. According to Takhtajans (1978) regionalization of the world flora, and referring to Goods (1974) and Wus (1979) scheme, the distribution patterns of Cyrtandroideae may be generalized as: (1) Pantropics, with 3 genera; (2) Palaeotropics, with 47 genera; and (3) North Temperate, with 27 genera. Tropical Asia (Indo Malaysia) is the centre of variation and diversity of the Cyrtandroideae, where the most primitive taxa, with the chromosome number of n=8 or n=9, and all of the four tribes exist, and where more genera(50) and species (1200 odd) are found than elsewhere. Among the four tribes of the Cyrtandroideae, only two tribes are distributed west of India. Three European genera with six species, confined to the Mediterranean, belong to one tribe, Didymocarpeae. Of 10 African and Madagascar genera, 9(7 endemic) belong to Trib. Didymocarpeae, 1 to Trib. Klugieae, and a11 of 168 African and Mada gascar species are not outside both of these regions. 2. Disjunct distribution and dispersal In Trib. Klugieae, two species of Epithema are found disjunctly in west Africa, and one species of Rhynchoglossum, R. azureum, is disjunct in tropical America, from southern Mexico to northern Peru. Their closely allied species and neighbouring genera are in tropical Asia. Rhynchoglossun azureum has a close relationship with R. notonianum, which is located in India and Sri Lanka, so it is hypothesized that Rhyncho glossum existed in north Africa, where there were tropical rain forests similar to those in Malaysia during the Tertiary. The author noticed that seeds of R. obliquum from tropical areas of southern Yunnan can still germinate after seven months at normal temperature. Most seeds of this genus are not only long lived but very tiny (0.3～0.4 mm long), and can be dispersed by wind or birds (epizoochore through the agency of mucus). One or two species of Rhipsalis in Cactaceae was carried by birds from south America to Madagascar, the Mascarene Islands and Sri Lanka at an early period. This example indicates the possibility of this means of distribution. More than 200 species from the volcanic islands of the Polynesian region, including the Hawaiian Islands,all belonging to Cyrtandra, were obviously spread by birds from tropical Asia during an earllier period. The distribution of two species of Boea and one species of Cyrtandra in northeast Queensland shows that some early taxa of the genera entered Yorke Peninsua from New Guinea when the sea level was lower during the Quaternary glaciations The modern vicarious distribution patterns of the two subfamilies indicate that the main taxa of the family were produced during the course of the continental drift and the climatic and environmental changes. According to the principle of common origin, the ancestor of Gesneriaceae appeared most probably not later than the late Cretaceous, and might be traced back to the Mid Cretaceous. 3. Some problems about evolutionary tendencies In general, the actinomorphic corolla precedes the bilabiate one, and the flower with stamens all fertile precedes those with 1 or 3 staminodes (Ivanina, 1965; Wang, 1989、 1992). In some diandrous genera of Cyrtandroideae, 4 or 5 fertile stamens may occur exceptionally, and are associated with a more or less regular corolla. The exceptional appearances may possibly be atavistic, not representing the main evolutionary tendencies. In the genus Aeschynanthus, pollen grains of Sect. Haplotrichum and Sect. Diplotrichum, whose corollas usually have indistinct bilabiate limbs, are comparatively small, but large in sections Microtrichium, Xanthanthos and Aeschynanthus, whose corollas have distinct bilabiate limbs. 4. The relationships of the four tribes he tribes Cyrtandreae, Trichosporeae and Didymocarpeae are closely related (Kvist and Pedersen, 1986). Some terrestrial plants of Trib. Trichosporeae (e.g.Anna and Lysionotus Sect. Didymocarpoides), in which the seeds have subulate appendages at their ends, may represent the intermediate links between tribes Didymocarpeae and Trichosporea.Boeica and Hexatheca form natural links between the tribes Cyrtandreae and Didymocarpeae. The tribes Didymocarpeae and Klugieae probably originated from a common ancestor at an early stage in the evolution of the family.     

云南哀牢山国家级自然保护区蕨类植物区系地理研究

通过野外调查和资料整理分析,哀牢山国家级自然保护区共有蕨类植物48科,118属,446种(包括变种和变型)。优势科为鳞毛蕨科、水龙骨科和蹄盖蕨科,优势属为耳蕨属、蹄盖蕨属、鳞毛蕨属和卷柏属。区系分析结果表明:该蕨类区系是亚热带性质的区系;热带亚洲成分随着海拔的升高,比例逐渐降低,而中国-喜马拉雅成分随着海拔的升高逐渐增加;地理成分的东西坡差异不明显;该蕨类区系与喜马拉雅地区和热带亚洲的关系较密切,而与日本的关系较疏远;该蕨类区系具有较丰富的中国特有成分;哀牢山明显处于滇西北、滇东南这两大中国特有多样性中心之间,成为联系的纽带。     

Evolution of bird communities in the Neogene of Central Asia,with a review of the Neogene fossil record of Asian birds

A complete taxonomic review of Neogene birds of continental Asia is provided. To date, avifauna from the latter half of the Miocene and Pliocene of Central Asia (Mongolia and adjacent regions of Inner Asia) are most thoroughly investigated. Available data enable a reconstruction of successive replacement of Early and Middle Miocene avifaunas by communities of the Recent type. Middle Miocene avifaunas of Mongolia include a great number of extinct genera and species, many of which were widespread in Eurasia. Extant genera became dominant in the Late Miocene and taxa close to living species appear in the Late Pliocene fossil record. Late Pliocene communities of birds of Central Asia were complex in genesis, composed of Miocene relicts (Struthio), immigrants from the European regions of the Palearctic (phasianid Plioperdix), North American immigrants (Calcarius), and also autochthonous elements, the origin of which is apparently connected with the arid belt of Central Asia (diverse passerines).