<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom" xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005">
<channel xmlns:cfi="http://www.microsoft.com/schemas/rss/core/2005/internal" cfi:lastdownloaderror="None">
<title cf:type="text"><![CDATA[ -->Special Column: Evolutionary Systematics]]></title>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Nova classification specierum sinensium <i>Pellioniae</i>(Urticaceae)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601005&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[(1)According to the various morphological differences between the two genera, <i>Pellionia</i> and <i>Elatostema</i>, enumerated in the present paper,the genus <i>Pellionis</i> is considered more primitive and to be derived from the genus <i>Pilea</i> before the genus <i>Elatostema</i>.(2)The genus <i>Pellionia</i> is subdivided into five sections. The genus <i>Elatostemoides</i> described by C. B. Robinson is relegated to sectional rank and treated as a section under <i>Pellionia</i> near its primitive group,sect. <i>Pileoides.</i> Besides,a new section related to sect. <i>Elatostemoides</i>,sect. <i>Leiolaena</i>,is described. On the basis of the evolutionary trends of the leaves,leaf nervation,pistillate inflorescences,pistillate tepals and achenes a putative phylogenetic tree showing the relationships among the infrageneric groups of the genus <i>Pellionia</i> is provided.(3)The infrageneric taxa of <i>Pellionia</i> in China are revised. Thirty-two species,one subspecies and seven varieties are recognized. They are keyed,described and in most cases illutrated,and are classified into four sections,two subsections,and nine series. Of them,except for sect. <i>Leiolaena</i> just mentioned above,two subsections,five series,two species and three varieties are described as new. The specific statuses of <i>Pellionia tsoongii,P. crispulihirtella,P. subundulata,P. minima</i> and <i>P. funingensis</i>,which were reduced into synonymy in 2003,are reinstated here. Besides,the brief taxonomic history and geographical distribution of the genus <i>Pillionia</i> in China are given.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[WANG Wen-Tsai]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Wen-Tsai</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601005&flag=1]]></guid><cfi:id>9</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Notes on Carex (Cyperaceae) from China (IV): the identity and revision of sect. Infossae]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601006&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Carex sect. Infossae S. W. Su was recently described from Anhui and Jiangsu provinces of East China，containing two species with one variety： C. infossa var. infossa，C. infossa var. extensa and C. minuticulmis. According to the sectional description，fifteen additional species and two varieties should be placed in this section. Based upon literature survey，specimen examination，field work，and SEM observation of perigynia and achenes，a concise table of different treatments between Florae Reipublicae Popularis Sinicae and Flora of China was provided，as well as the morphological characters distinguishing these taxa and micromorphology of perigynia and achenes for the selected taxa were compared. Among the diagnostic characters，arrangement of spikes and perigynium indumentum are inseparable from each other，and two species in sect. Infossae are consequently recognized in the present paper. Carex elmeri，C. granifera，C. minuticulmis，C. shanghaiensis，C. blinii subsp. shanghaiensis，C. sublateralis，C. taihokuensis and C. tatsutakensis were synonymized to C. blinii. Carex canaliculata，C. changmuensis，C. distantiflora，C. infossa，C. infossa var. extensa，C. lateralis，C. loheri，C. longerostrata var. exaristata，C. longerostrata var. hoi，C. lyi，C. macrandrolepis，C. sharyotensis were reduced as synonyms to C. oxyphylla.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[CEN Jia-Meng1， JIN Shui-Hu2， JIN Xiao-Feng1*]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CEN Jia-Meng1， JIN Shui-Hu2， JIN Xiao-Feng1*</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601006&flag=1]]></guid><cfi:id>8</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[You win some you lose some: updated generic delineations and classification of Gesneriaceae-implications for the family in China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601007&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Over the last two decades molecular phylogenetic research on Gesneriaceae has greatly advanced our understanding of species relationships and generic delimitations. It has allowed the proposal of a new classification of the family that is thought to reflect the natural relationships of the taxa better than traditional morphological classifications. Dramatic taxonomic changes were implemented affecting the classification of Gesneriaceae in China. Many traditional genera have been split， merged or newly defined. Additionally， new genera have been established based on recently collected material， illustrating on the one hand gaps in fieldwork in China， and on the other hand the biological richness of the Gesneriaceae in China. Here， we summarize and present an overview of our work and the taxonomic consequences.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[M&#214;LLER Michael<sup>1*</sup>, WEI Yi-Gang<sup>2</sup>, WEN Fang<sup>2</sup>, CLARK John L.<sup>3</sup>, WEBER Anton<sup>4</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>M&#214;LLER Michael<sup>1*</sup>, WEI Yi-Gang<sup>2</sup>, WEN Fang<sup>2</sup>, CLARK John L.<sup>3</sup>, WEBER Anton<sup>4</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601007&flag=1]]></guid><cfi:id>7</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Numerical taxonomy of the genera <i>Daphne</i> and <i>Wikstroemia</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601008&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Daphne</i> and <i>Wikstroemia</i> are members of subfamily Thymelaeoideae which belongs to Thymelaeaceae. There are 95 species(varieties)in genus <i>Daphne</i>, 52 of which distribute in China<i>.</i> There are 70 species(varieties)in genus <i>Wikstroemia</i> and 49 species(varieties)can be found in China. Southwest China is the species diversification center of the two genera. Petals of <i>Daphne</i> and <i>Wikstroemia</i> degenerate and usually form circular disc or linear disc scale. Conventionally, the shape of disc and type of fruit were used as crucial characters to separate the two genera. The circular disc frequently occurs in <i>Daphne</i> while linear disc scale occurs in <i>Wikstroemia</i>. Meanwhile, fruit is usually succulent berry in <i>Daphne,</i> but <i>Wikstoemia</i> has dry or leathery fruit, and sometimes enclosed by persistent calyx. However, alternational characters among species of the two genera have been reported and some species have both kinds of characters. In this study, 32 morphological characters were used in the numerical taxonomy of 77 species(varieties)from genus <i>Daphne </i>and 62 species(varieties)from genus <i>Wikstroemia </i>with<i> </i>clustering and principal component analysis.<i> </i>UPGMA clustering results revealed that neither genera formed monophyletic group species from the two genera clustered together. In the principal components analysis, the cumulative percent of the first three principal components presented 35.56%, while the conventional taxonomic characters, such as the disc shape, phyllotaxy and the fruit type, contribute minor effects on the first three components. So, taxonomic distinguishable characters of the two genera could not separate them clearly. Three-dimensional scatter plots based on principal components analysis revealed that species from both genera embeded with each other and did not separate two genera as monophyletc group. Neither clustering analysis nor principal components analysis supported the traditional taxonomy that <i>Daphne</i> and <i>Wikstroemia</i> were naturally monophyletic groups.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[ZHANG Yong-Zeng<sup>1,2</sup>, SUN Wen-Guang<sup>1,2</sup>, JIANG Xin<sup>1,2</sup>, 
LI Zhi-Min<sup>1,2</sup>, ZHANG Yong-Hong<sup>1,2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Yong-Zeng<sup>1,2</sup>, SUN Wen-Guang<sup>1,2</sup>, JIANG Xin<sup>1,2</sup>, 
LI Zhi-Min<sup>1,2</sup>, ZHANG Yong-Hong<sup>1,2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601008&flag=1]]></guid><cfi:id>6</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Pollen morphology of Chinese Begonia (Begoniaceae) and its taxonomical significance]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601009&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Begonia L. is the sixth biggest genus of flowering plants in the world and a major genus in the family Begoniaceae. It is complicated in current section delimitation and more morphological characters are needed for critical revaluation within the genus. In present study，we selected 21 species from sections Coelocentrum，Begonia，Platycentrum and Reichenheimia of Begonia mainly distributed in China. Using the method of scanning electron microscopy (SEM)，the pollen morphology was carefully examined and its systematic significance was discussed. The results showed that the common palynological characters of studies taxa were exhibited as monads，radially symmetrical，isopolar，3-zono-colporate and perprolate to prolate. For non-metric multidimensional scaling (NMDS) analysis，nine stable pollen characters were selected and coded as unordered and unweighted. The results supported that these sections were not monophyletic groups and the useful palynological features for this study were the pollen sides，outline of the poles，colpus，exine ornamentation，and margo. According to the ornamentation of margo，the studied taxa can be divided into two groups：(A) without margo and psilate margo，(B) regulate，exquisitely regulate and coarsely regulate margo. In relation to Group B，the taxa with regulate and exquisitely regulate grains were gathered while the taxa with coarsely regulate margo were located between Group A and B. It indicated that the feature of margo was exhibited as a transition，from without margo and psilate margo，along coarsely regulate margo to exquisitely regulate. Therefore，it is worthy to pay more attention on the feature of margo and increase more taxa of the genus in further studies.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[DONG Li-Na*， LIU Yan， CAO Xiao-Yan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>DONG Li-Na*， LIU Yan， CAO Xiao-Yan</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601009&flag=1]]></guid><cfi:id>5</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Taxonomic significance of the pollen morphology of sect. Racemosae (Impatiens)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601010&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Section of Racemosae Hook. f. et Thomson, blonging to subg. Impatiens, Impatiens, Balsaminaceae, most of them distributed in South China and with a part of species radiated to southern slope of Himalaya and Europe. The species of this section are characterized by racemose inflorescences with many flowers, 2 lateral sepals, 5-carpellated ovary, linear capsule fruits with multiple seeds, subobovoid, and surface of seed with finger-like protuberance appendages, which well circumscribe this section from others of Impatiens. Pollen studies in previous works indicated that morphological characters of pollen grains were of valuable in subdivision of Impatiens and circumscription of Impatiens species. However, the species carried out pollen studies in sect. Racemosae are few concerned. In order to study the pollen grain characters and clarify their taxonomic significance of pollen morphology characters, 21 species from sect. Racemosae were sampled and investigated under Scanning Electron Microscope in this study. The observation results indicated that the species of sect. Racemosae were characteristic of 4-colpate pollen grain, zygomorphic, and oblong, long-oblong or sub-quadrate in polar view. The long equatorial view of pollen grain were elliptic to oblong, short equatorial view of pollen grains were elliptic; and the ratio of length of long equatorial axis to short one were mostly between 1.4-2.4. The exine of pollen grains were of reticulate ornamentation with lumina even in polar view or uneven equatorial view. The muri of lumen were smooth or sinuate towards margin. There were granules in the lumina with different densities. The pollen morphology characters of sect. Racemosae showed little correlation with the gross morphological characters within this section. However, variation in the aspects of pollen shapes in polar view, the ratio between long equatorial axis and short equatorial axis, distribution of lumen, muri of lumen smooth or sinuate and the density of granules in the lumina and so on, were consensus within species expressed the taxonomical value in circumscription of species within sect. Racemosae.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[GUO Hui1 2，YAN Rui-Ya2，ZHANG Mei2，LUO Qiang3，
ZHANG Lin-Jing1，YU Sheng-Xiang2 *]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>GUO Hui1 2，YAN Rui-Ya2，ZHANG Mei2，LUO Qiang3，
ZHANG Lin-Jing1，YU Sheng-Xiang2 *</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601010&flag=1]]></guid><cfi:id>4</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Gametophyte development in <i>Onychium japonicum </i>and its systematic significance]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601011&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Onychium japonicum</i> falls into the category of <i>Onychium</i> Kaulf. of Sinopteridaceae; however, the alliance of <i>Onychium</i>remains controversial. In this study, the spores of <i>O. japonicum </i>were artificially cultured in the original habitat humus soil and improved Knop's nutrient solution in a constant temperature of 25 ℃ with 12 h of light and dark respectively per day and 2 500 lx of light intensity. Spore germination and gametophyte development were observed and recorded at every stage under the microscope.The results indicated that mature spores were tawny,tetrahedral,3-colporate,with fan-shaped equatorial view,perispore and reticulation on the surface of the exine. The germination procedure was Vittaria-type while the gametophyte development was Ceratopteris-type. The spores cultivated in either of the two substrates began to germinate about 7 d and their germination shared the same Vittaria-type. With multiple transverse fission,the original gametophyte cell gradually turned into 3-9 protonemata with cylindrical shape, thin perispore,lumpy lateral exine and numerous granular chloroplasts. After about 15 d,the spores developed into prothallial plates and most of prothallial plates appeare spatulate. And 25 d later, young prothalliums were formed but they were not symmetrical; meanwhile, the gametophytes developed were Ceratopteris-type. When the prothalliums were developing, branching protonemata were flourishing and gametophytes were becoming fasciculate without any trichome. The rhizoids of <i>O. japonicum</i>, occasionally branching and lacking chloroplasts, were unicellular and tubular. After about 45 d,antheridium, composed of a cap cell, a ring cell and a basal cell, emerged from the edge of several irregular prothalliums. When the antheridium became mature, the cap cell split and sperm spilt. The antheridium looked like a circle from the top and an oval or a short column from the side. About 60 d later, a large archegonium was clearly visible. Its base was bigger than the top. It looked like a coin from the top and a chimney from the side. Its neck consisted of four rows of cells. When the archegonium was fully developed, sperm entered and fertilized the egg cell inside. Half a month later, a young embryo could be clearly seen. About 90 d after sowing,the spores developed into juvenile sporophytes which were visible to the naked eye. It could be concluded from the findings that <i>O. japonicum</i> shared similar characteristics with<i> Pteris</i> of Pteridaceae in terms of gametophyte development. Therefore, <i>O. japonicum</i> could be classified into the Pteridaceae family. The study would provide evidence for the phylogenetic study of <i>O. japonicum</i> from the perspective of gametophyte development.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[DENG Xi-Chao]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>DENG Xi-Chao</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601011&flag=1]]></guid><cfi:id>3</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Adaptive evolution of the <i>ndh</i>F gene in the genus <i>Rheum</i>(Polygonaceae)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601012&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Rheum</i>, a highly diversified genus of Polygonaceae, comprising about 60 species, is mainly distributed in the mountainous and desert regions in Asia and Europe. Its high diversification in the Qinghai-Tibetan Plateau and adjacent areas,where approximately 40 species have been described,was suggested to result from the adaptive radiation triggered by the recent uplifts of the Qinghai-Tibetan Plateau and the quaternary climate oscillations. To further understand the molecular adaptation linked to <i>Rheum</i> radiation, the adaptive evolution of chloroplast <i>ndh</i>F gene belonging to 34 morphologically diversified species of the genus <i>Rheum</i> were tested by using the Phylogenetic Analysis Program in this study. The results showed that the pattern of phylogenic tree was a typical “paralleling” phylogeny, suggesting a radiative diversification. Three amino acid sites(188H,465H,551L)of NDHF subunit were identified under positive selection(<i>ω</i>&gt;1),and the secondary structures of NDHF subunit showed that the 188th amino acid was located in the α-helix. The changes of these adaptive sites may be associated with the evolution of NDH to adapt the extreme habitats of <i>Rheum</i> species caused by the extensive uplifts of the QTP and the quaternary climate oscillations.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[LI Jing-Jian<sup>1,2</sup>, LIU He-Xia<sup>2</sup>, MAO Shi-Zhong<sup>2</sup>, 
ZHAO Bo<sup>2,3</sup>, HUANG Shi-Xun<sup>2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Jing-Jian<sup>1,2</sup>, LIU He-Xia<sup>2</sup>, MAO Shi-Zhong<sup>2</sup>, 
ZHAO Bo<sup>2,3</sup>, HUANG Shi-Xun<sup>2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601012&flag=1]]></guid><cfi:id>2</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Pollination biology and the breeding system of <i>Plumbago auriculata </i>low seed-set ratio]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601013&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In order to explain the main reasons for the low natural seed-set ratio of <i>Plumbago auriculata</i>, which can contribute to the large-scale production of <i>P. auriculata </i>and also help to get rid of the situation that the seeds over-rely on the import from abroad at the same time. We attempted to measured the dynamic changes of the pollen viability by the method of TTC and the stigma receptivity and the method of Benzidine-H<sub>2</sub>O<sub>2 </sub>in two ways, which respectively focused more on the pollination biology and the breeding system. And we also estimated the type of the breeding system pollen-ovule ratio(P/O), and verified the out-crossing index(OCI)by the pollination experiments. The results of the experiment were as follows:(1)About <i>P. auriculata</i>, the maturity time of the L-type female organs and the S-type male organs,and also that of the L-type female organs and the L-type male organs overlaped a lot,there was no obvious difference in the maturity time between the female and the male organs. On the other hand,the maturity time of the S-type female organs and the L-type male organs,and also that of the S-type female organs and the S-type male organs overlaped a little,but the continuous blossoming pattern of <i>P. auriculata </i>reduced reproductive isolation caused by the different maturity time of the male and the female sexual organs.(2)The P/O of L-type was 502&#177;52.30,the P/O of S-type 482.7&#177;87.91,both the out-crossing index of the L-type and that of the S-type are 4. The result of the manual-controlled pollination experiments suggested that the breeding system of <i>P. auriculata </i>was obligate outcrossing and it had the feature of the heteromorphic incompatibility. To sum up,the reasons for the low natural seed-set ratio of <i>P. auriculata</i> were the combination of both internal and external factors. Among these factors,the short same maturity time of the male and the female sexual organs was not the main reason,while the strong self-incompatibility of <i>P. auriculata itself </i>might be the key internal factor to lead to the low natural seed-set ratio. Due to the breeding system of the obligate outcrossing,it was quite necessary for <i>P. auriculata </i>to had the pollination medium to lead to the successful pollination. However,the introduction environment and the original environment were distinctly different,in addition,the mode of the scattered blooming led to the cross-pollinator,which might be the key external factor of low success rate of outcrossing. In a conclusion,the improvement of the natural seed-set ratio of <i>P. auriculata </i>should mainly focus on overcoming the incompatibility of <i>P. auriculata </i>itself,and also properly bringing in some insects as the safe medium. This would provide the theoretical guidance and the application foundation for the expansion of this kind of species resource and also the acceleration of the promotion and the application.]]></description>
<pubDate>2016/2/3 0:00:00</pubDate>
<category><![CDATA[Special Column: Evolutionary Systematics]]></category>
<author><![CDATA[WU Pei-Wen<sup>1</sup>, GAO Su-Ping<sup>2*</sup>, ZHANG Shuo<sup>1</sup>, ZHAO Zhi-Hui<sup>1</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WU Pei-Wen<sup>1</sup>, GAO Su-Ping<sup>2*</sup>, ZHANG Shuo<sup>1</sup>, ZHAO Zhi-Hui<sup>1</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=201601013&flag=1]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
</channel>
</rss>