<?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[ -->Systematic Evolution and Biodiversity]]></title>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[秦巴山区野百合表型多样性]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140601&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2015/12/15 11:54:15</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140601&flag=1]]></guid><cfi:id>32</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[西南地区野生狗牙根种质资源的SSR与AFLP联合分析]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140602&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2015/12/15 11:54:15</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140602&flag=1]]></guid><cfi:id>31</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[广西毛竹种质资源AFLP分析]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140603&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2015/12/15 11:54:15</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140603&flag=1]]></guid><cfi:id>30</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[蓝花丹的花部形态二态性及自交不亲和特性]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140604&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2015/12/15 11:54:15</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140604&flag=1]]></guid><cfi:id>29</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[南方红豆杉小孢子发生与雄配子体发育]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140605&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2015/12/15 11:54:15</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140605&flag=1]]></guid><cfi:id>28</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[新疆特有珍稀灌木银沙槐繁育系统研究]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140606&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2015/12/15 11:54:15</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140606&flag=1]]></guid><cfi:id>27</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[濒危药用植物短柄乌头及其近缘种的核型研究]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140607&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2015/12/15 11:54:15</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140607&flag=1]]></guid><cfi:id>26</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Phylogenetic analysis of <i>Ranunculus cantoniensis</i> 
complex based on low-copy nuclear gene <i>GBBSI</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140501&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Evolutionary relationship of <i>Ranunculus cantoniensis</i> polyploid complex and its allied species was complicated,and hybridization and polyploidization occurred simultaneously in this complex. It was necessary to explore the speciation and dispersal processes of high-ploid taxa. First cloned partial sequence of <i>GBBSI</i> gene,then phylogenetic tree and network were constructed using the introns of <i>GBBSI</i> gene,and proved that the introns of <i>GBBSI</i> gene were suited to study phylogenetic relationship of <i>Ranunculus</i>. The results showed that <i>R. repens</i> closely associated with<i> </i>polyploid complex,participating in the origin and evolution of polyploid complex; <i>R. cantoniensis</i> originated from hybridization of <i>R. chinensis </i>and <i>R. silerifolius </i>var<i>. silerfolius</i>,<i>R. sieboldii</i> originated from hybridization of <i>R. chinensis</i> and<i> R. repens</i>,<i>R. repens </i>might originated from hybridization of <i>R. chinensis</i> and <i>R. silerifolius </i>var<i>. dolicathus</i>; <i>R. chinensis</i> was a key species in this complex,which may play an important role as a pivotal genome.]]></description>
<pubDate>2015/12/15 11:20:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[WANG Qun, LI Tong-Jian, HAN Xing-Jie, LIAO Liang, XU Ling-Ling<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Qun, LI Tong-Jian, HAN Xing-Jie, LIAO Liang, XU Ling-Ling<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140501&flag=1]]></guid><cfi:id>25</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Flowering characteristics and pollination biology of 
rare and endangered <i>Kolkwitzia amabilis</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140502&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The floral dynamics,pollen viability,stigma receptivity,floral visitors and their behaviors,pollen ovule rate(P/O),outcrossing index(OCI)of <i>ex-situ</i> conservation rare and endangered plant of <i>Kolkwitzia amabilis </i>were studied. The main results were as follows:the anthesis of <i>K. amabilis</i> was about 7 days,the population flowering was about 14 d. Pollen viability achieved the maximum at 2～3 h after flowering,about 90%. After 3 days,no pollen viability was detected. Stigma shown acceptance during the entire anthesis and achieved the maximum at the second day after flowering. The pollen ovule rate(P/O)was 398.1&#177;63.7 and the outcrossing index(OCI)was 3,the results indicated that the breeding system was outcrossing with partial self-compatibility and sometimes pollinators were needed. More than 10 species of insects were observed to visit the inflorescences of <i>K. amabilis</i>. The most common floral visitors were bees and halictids of Hymenoptera,also a small amount of hoverflies of Diptera and a few of bumblebees and lepidopteron,among which Apidae insects were the effective pollinators. No seed was detected in <i>K. amabilis</i> in the <i>ex-situ</i> environment,further study of which is still needed.]]></description>
<pubDate>2015/12/15 11:20:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[MAO Shao-Li<sup>*</sup>, ZHOU Ya-Fu, LI Si-Feng, ZHANG Ying]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>MAO Shao-Li<sup>*</sup>, ZHOU Ya-Fu, LI Si-Feng, ZHANG Ying</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140502&flag=1]]></guid><cfi:id>24</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Drup and seed morphology of the <i>Berchemia</i> and <i>Berche-
miella</i>(Rhamnaceae)and its systematic significance]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140503&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Drupes and seeds of 17 species in <i>Berchemia </i>and <i>Berchemiella </i>(Rhamnaceae)were investigated under SEM and LM. The present study indicated that the drupe of <i>Berchemiella</i> is 1-loculed with one seed,and the drupes are 2-loculed,each locule with one seed in the most species of <i>Berchemia</i>. However,the drupe is 2-locular,but one locule big and with single seed,another locule small and without seed in <i>B. polyphylla</i>. This species may be a transitional taxon between <i>Berchemiella </i>and<i> Berchemia.</i> Seed shape of <i>Berchemia</i> and <i>Berchemiella </i>is usually irregularly long-ellipsoidal. Seed coat sculpture can be divided into three major types,i. e. smooth or almost smooth,indistinctly or sparsely striate with low striae,distinctly striate or sulcate. The differences in seed coat sculpture among species are of taxonomic significance for identifying some species in these two genera.]]></description>
<pubDate>2015/12/15 11:20:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[WEI Ruo-Xun<sup>1,2</sup>, ZHANG Zhi-Yun<sup>3</sup>, CHEN Yi-Lin<sup>4</sup>, Joongku Lee<sup>5*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WEI Ruo-Xun<sup>1,2</sup>, ZHANG Zhi-Yun<sup>3</sup>, CHEN Yi-Lin<sup>4</sup>, Joongku Lee<sup>5*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140503&flag=1]]></guid><cfi:id>23</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Genetic diversity at chloroplast microsatellites(cpSSR)
in <i>Abies fanjingshanensis</i> and <i>A. yuanbaoshanensis</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140504&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Abies fanjingshanensis</i> and <i>A. yuanbaoshanensis</i> are critically endangered plants. We used chloroplast microsatellite marker to compare the genetic diversity of <i>A. yuanbaoshanensis</i> and <i>A. fanjingshanensis</i> with a widely distributed species <i>A. fargesii </i>var. <i>faxoniana</i>. A total of 21 alleles and 35 haplotypes was detected in 249 individuals from 3 pairs of primer(Pt63718,Pt30204 and Pt71936). The number of haplotypes(<i>No</i>),effective number of haplotypes(<i>Ne</i>)of <i>A. fanjingshanensis</i>(<i>No</i>=12,<i>Ne</i>=3.92)and <i>A. yuanbaoshanensis</i>(<i>No</i>=9,<i>Ne</i>=3.28)were lower than <i>A. fargesii </i>var. <i>faxoniana</i>. <i>A. fanjingshanensis</i> and <i>A. yuanbaoshanensis</i> had less rare haplotypes. The haplotype diversity(<i>He</i>)of <i>A. fanjingshanensis</i>(<i>He</i>=0.75)and <i>A. yuanbaoshanensis</i>(<i>He</i>=0.70)were also lower than <i>A. fargesii </i>var. <i>faxoniana</i>(<i>He</i>=0.97). <i>A. fanjingshanensis</i> and <i>A. yuanbaoshanensis</i> had a relatively low level of genetic diversity at chloroplast microsatellite.]]></description>
<pubDate>2015/12/15 11:20:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[WEI Fan<sup>1,2</sup>, ZHANG Guang-Rong<sup>1</sup>, QIN Yong-Xian<sup>1</sup>, 
LIUFU Yong-Qing<sup>1</sup>, TANG Shao-Qing<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WEI Fan<sup>1,2</sup>, ZHANG Guang-Rong<sup>1</sup>, QIN Yong-Xian<sup>1</sup>, 
LIUFU Yong-Qing<sup>1</sup>, TANG Shao-Qing<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140504&flag=1]]></guid><cfi:id>22</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Study on aquatic plant diversity changes 
in Caohai plateau wetland]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140505&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Based on the data of literature and field survey,aquatic plant diversity of Caohai plateau wetland was analyzed. The results showed that the number of <i>Grus nigricollis</i> wintering in Caohai had increased from 223 in 1985 to 506 in 2005,and 1 000 in 2011. And the number of families and genera of the aquatic plant had significantly increased. There were 49 species subjected to 37 genera of 25 families in 2005,in which 11 species and 10 genera and 5 families were new record contrast with 1983. The Comm. of <i>Scirpus yagara,S. tabernaemontani,</i><i>Leersia hexandra</i>,<i>Juncellus serotinus</i> and <i>Juncus effusus</i> became main dominant communities along the lakeside. Aquatic vegetation had been changing in the direction of marsh vegetation. The speed of Comm. of <i>Alternanthera sessilis</i> spread had been faster than anticipated,particularly seriously in the east,southeast and northeast of Caohai wetland. Interference is the main reason for the change of biodiversity in Caohai. Reducing human disturbance,maintaining a stable surrounding environment of Caohai are important measures to protect and increase the diversity of aquatic plants.]]></description>
<pubDate>2015/12/15 11:20:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[TANG Jin-Gang<sup>2</sup>, LI Wei-Jie<sup>2</sup>, ZHOU Chuan-Yan<sup>1,2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>TANG Jin-Gang<sup>2</sup>, LI Wei-Jie<sup>2</sup>, ZHOU Chuan-Yan<sup>1,2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140505&flag=1]]></guid><cfi:id>21</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Screening of microsatellite loci by cross-species 
amplification and their use in <i>Cycas 
fairylakea</i>(Cycadaceae)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140506&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Simple sequence repeat(SSR)markers developed from <i>Cycas rumphii,C. changjiangensis</i> and <i>C. hainanensis</i> were cross-species amplified in genomic leaf DNA of <i>C. fairylakea</i>. The positive PCR productions were cloned and sequenced. Seven loci consistently yielded the predicted size ranges. Of these loci,three were polymorphic and confirmed as simple sequence repeat(SSR)loci in <i>C. fairylakea</i>. They were utilized to investigate the genetic diversity among four wild populations of <i>C. fairylakea</i>. The number of alleles per locus ranged from 2 to 5,and the observed and expected heterozygosities varied from 0.000 to 0.667 and from 0.000 to 0.610,respectively. Pairwise F<sub>st</sub> varied from 0 to 0.382. In the whole,<i>C. fairylakea</i> has low levels of genetic variation within populations and high variation across populations. The STRUCTURE analysis indicated that the four <i>C. fairylakea</i> populations could be subdivided into three different hypothetical genetic clusters(K). The BOTTLENECK results suggested that no populations had faced recent significant bottleneck.]]></description>
<pubDate>2015/12/15 11:20:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[WANG Yun-Hua, LI Nan, CHEN Ting, DENG Huan-Xiang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Yun-Hua, LI Nan, CHEN Ting, DENG Huan-Xiang</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140506&flag=1]]></guid><cfi:id>20</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The traditional knowledge of Dong Nationality 
utilizing plant resources in Qiandongnan]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140507&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Based on viewpoint of ethnobotany, the Dong Nationality's traditional knowledge of utilizating plant resources in Qiandongnan(southeast of Guizhou Province)were studied, including plant resources associated with the eating habits,commonly used medicine,traditional residence,living appliances,mode of production,folk belief and worship of nature and so on. And the ways of knowing,utilizing and conserving plant resources in Dong community there were analyzed,too. The results showed that there were about 122 species of plants in everyday life of Dong people in Qiandongnan. Plant resources played a very important role in their physical and mental life. The plant resources include utilized for food,pharmaceutical,dyestuff,faith,dwelling and living utensils etc. Dong people possessed a lot of knowledge and experience in utilizing plants and had created specificity ethnic culture. Many of their traditional knowledge and experience still have important values of research and reference for exploitation and utilization of plant resources in their own or other ethnic populations.]]></description>
<pubDate>2015/12/15 11:20:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[ZHOU Chuan-Yan<sup>1,2</sup>, LU Yi<sup>3</sup>, WANG Ji-Hong<sup>4</sup>, CHEN Xun<sup>3*</sup>,
 LUO Shi-Qin<sup>2</sup>, TANG Jin-Gang<sup>2</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHOU Chuan-Yan<sup>1,2</sup>, LU Yi<sup>3</sup>, WANG Ji-Hong<sup>4</sup>, CHEN Xun<sup>3*</sup>,
 LUO Shi-Qin<sup>2</sup>, TANG Jin-Gang<sup>2</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140507&flag=1]]></guid><cfi:id>19</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[收稿日期: 2013-10-14修回日期: 2013-12-15
 基金项目: 焦作市科技计划项目(201204001)
 作者简介: 张安世(1965-),男,河南博爱人,教授,主要从事植物分子生物学研究,(E-mail)aszhang1212@163.com。
<sup>*</sup>通讯作者 Genetic diversity of the rare and endangered plant 
<i>Opisthopapus taihangensis</i> detected by ISSR analysis]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140421&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Using inter-simple sequence repeat(ISSR)analysis,the genetic diversity of 11 natural populations of <i>Opisthopapus taihangensis </i> were investigated. Ten ISSR primers were used to amplify 122 individuals of 11 natural populations. Using these primers,150 DNA fragments were produced,and 149 bands were polymorphic loci(<i>PPL</i>=99.33%). The result of POPGENE analysis indicated that genetic diversity of <i>O. taihangensis </i>was higher(<i>I</i>=0.2149,<i>H</i>=0.3455). Daxitian possessed the highest level of genetic diversity while Lingchuan population exhibited the lowest level of genetic diversity. A high level of genetic differentiation among 11 populations was detected based on Nei's genetic diversity analysis(<i>Gst=</i>0.2566,<i>Nm=</i>1.4488). The main factors responsible for the high degree of genetic differentiation among populations may result from habitat fragmentation and barriers of gene flow. Based on genetic information available for <i>O. taihangensis</i>,some conservation strategies proposed.]]></description>
<pubDate>2015/12/15 11:19:56</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[ZHANG An-Shi<sup>1*</sup>, ZHAO Li-Xin<sup>2</sup>, LIU Ying<sup>1</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG An-Shi<sup>1*</sup>, ZHAO Li-Xin<sup>2</sup>, LIU Ying<sup>1</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140421&flag=1]]></guid><cfi:id>18</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Deceptive pollination of a saprophytic 
Orchid, <i>Eulophia zollingeri</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140422&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Eulophia zollingeri</i> is one typical saprophytic species in Orchidaceae. Pollination biology of saprophytic orchid has been poorly studied. In order to reveal the significant pollination mechanism of <i>E. zollingeri</i>,broaden our knowledge on reproductive biology of saprophytic orchid,the floral biology and visitation of this plant were studied in Yachang Orchid National Nature Reserve,the west of Guangxi Province,China. <i>E. zollingeri</i> flowers were self-compatible but pollinators were required to achieve effective pollination; <i>Nomia viridicinctula </i>Cockerell was the only effective pollinator; Foraging in the flowers mainly occurs in three periods:8.6% in 9:00-11:30 AM,80.2% in 11:30 AM-14:00 PM,11.2% in 14:00-15:30 PM; The flowers volatilize sweet floral fragrance under strong sunshine in the midday. We considered <i>E. zollingeri</i> attracts pollinators into flowers for foraging by the dizzy floral fragrance and bright yellow color in labellum,then the matchable sizes of flowers and the pollinators in functional morphology provides dynamic support for effective pollination. The pollinators received no reward in the whole pollination procedure,it was food-deceptive pollination mechanism.]]></description>
<pubDate>2015/12/15 11:19:56</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[ZHANG Zi-Bin<sup>1,2,3</sup>, YANG Mei <sup>2,3</sup>, ZHAO Xiu-Hai<sup>1</sup>, NI Shi-Dong<sup>2</sup>,
 YANG Fei-Peng<sup>2</sup>, CHEN Qiao-Qiao<sup>2</sup>, HUANG Bo-Gao<sup>2,3*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Zi-Bin<sup>1,2,3</sup>, YANG Mei <sup>2,3</sup>, ZHAO Xiu-Hai<sup>1</sup>, NI Shi-Dong<sup>2</sup>,
 YANG Fei-Peng<sup>2</sup>, CHEN Qiao-Qiao<sup>2</sup>, HUANG Bo-Gao<sup>2,3*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140422&flag=1]]></guid><cfi:id>17</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Identification of Kumquats(<i>Fortunella crassifolia</i>)
new varieties by ploidy analysis and AFLP]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140423&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[To determine the genetic diversity of Kumquats new varieties. We employed ploidy analysis and 12 pairs of AFLP primer combinations on 8 Kumquats varieties. Ploidy analysis confirmed that Huapijingan was a diploid,Jingan Ⅱ was a tetraploid. AFLP results showed that: A total of 341 major AFLP bands were observed,and 95 band were polymorphism. Genetic similarities among all taxa ranged from 0.867 to 0.985. 8 varieties could be divided. Phenetic trees based on genetic similarities(UPGMA,N-J)were similar to known taxonomic relationships. the genetic similarity coefficient between Huapijingan and Jingan was 96.8%,the genetic similarity coefficient between Jingan Ⅱ and Jingan was 95.8%,the genetic similarity coefficient between Jingan Ⅱ and Huapijingan was 95.7%. Jingan Ⅱ and Huapijingan could be used as new cultivar.]]></description>
<pubDate>2015/12/15 11:19:56</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[FU Cui-Na, XIAO Yuan-Hui, GAN Hai-Feng<sup>*</sup>, LEI Xin-Nan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>FU Cui-Na, XIAO Yuan-Hui, GAN Hai-Feng<sup>*</sup>, LEI Xin-Nan</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140423&flag=1]]></guid><cfi:id>16</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Application of DNA barcoding in cannabic identification]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140424&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[To study the feasibility of DNA barcoding on cannabic species identification,DNA were extracted from sixty cannabis plants' leaves(cultivated cannabis from Inner Mongolia,Heilongjiang,Shanxi Yan'an and Yulin,wild cannabis from Xinjiang Manas,six male and female cannabis from each region),used ribosomal DNA intergenic region ITS2 universal primers and cpDNA psbA-trnH primer for PCR amplification,then sequenced in both directions,the results compared to manual correction and finally for Blast comparison. ITS2'amplified sequences of all samples were completely consistent,but psbA-trnH'amplified sequences varied greatly,which were detected eight kinds of cpDNA haplotypes. MEGE 5.1 software was used to calculate the genetic distance between species,and build NJ phylogenetic trees which could effectively separate the five regions of cannabic samples. So DNA barcoding on cannabic species identification was proved to have viability,but the accuracy,reliability and possibilities of identification of its origin and species need further research.]]></description>
<pubDate>2015/12/15 11:19:56</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[SONG Bing-Ke<sup>1</sup>, YANG Xue-Ying<sup>2</sup>, NI Ping-Ya<sup>3</sup>, 
PEI Li<sup>2*</sup>, ZHANG Ying<sup>2</sup>, XU Xiao-Yu<sup>2</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SONG Bing-Ke<sup>1</sup>, YANG Xue-Ying<sup>2</sup>, NI Ping-Ya<sup>3</sup>, 
PEI Li<sup>2*</sup>, ZHANG Ying<sup>2</sup>, XU Xiao-Yu<sup>2</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140424&flag=1]]></guid><cfi:id>15</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[<i>Clematis dongchuanensis</i>, a new species 
of Ranunculaceae from Yunnan]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140301&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[A species of the genus <i>Clematis</i>(Ranunculaceae),<i>C. dongchuanensis</i>,is described as new from northeastern Yunnan. In having simple leaves,erect sepals and puberulous filaments and anthers of stamens this species is related to <i>C. repens</i> Finet &amp; Gagnep.,and from the latter differs in its cordate-ovate and coarsely dentate leaves,dichotomous cymes,and obtuse,not apiculate apexes of anthers.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[WANG Wen-cai]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Wen-cai</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140301&flag=1]]></guid><cfi:id>14</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The genomic imprinting in ployploid plants]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140302&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Polyploidy is prevalent in nature, which reveals that there is an evolutionary advantage of having multiple sets of genetic materials for adaptive evolution in plants. When a new polyploid formed,many of genome-wide changes arose following the onset of polyploid formation,whereas others emerged on a longer evolutionary timescale. Owing to the influence of genetic and epigenetic mechanisms,the contributions of the parental genomes to the new formed polyploid were not equal. The dominance advantage of the biased parental genome was described as genomic imprinting. Genomic imprinting in polyploid plants showed the genome sequence of bias eliminating,imbalanced gene expression and gene silencing,which appeared to be caused by genome merger and epigenetic mechanisms: DNA methylation,nuclear dominance. This paper aimed to provide a reference for the research of genome evolution and polyploid breeding in plants.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[LIU Yu-Ling<sup>1,2</sup>, HAN Xing-Jie<sup>2</sup>, LI Tong-Jian<sup>2</sup>, XU Ling-Ling<sup>2</sup>, LIAO Liang<sup>2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIU Yu-Ling<sup>1,2</sup>, HAN Xing-Jie<sup>2</sup>, LI Tong-Jian<sup>2</sup>, XU Ling-Ling<sup>2</sup>, LIAO Liang<sup>2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140302&flag=1]]></guid><cfi:id>13</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Analyses on the types of copy and evolutionary 
relationships of ITS sequence of <i>Phormidium</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140303&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The coevolution of the ITS sequences hasn't been fully accomplished leading to multiple types of copy in cyanobacteria,while the distribution rule of ITS copy in cyanobacteria are unclear. We used <i>Phormidium</i> strains picked up from Suzhou districts and 12 other strains selected from Genebank as the materials to study the characteristics and the evolutionary relationships among different types of copy. The results showed that the PCR product of ITS of <i>Phormidium</i> had single band(i. e. ITS-IA type or ITS-I type)or two bands(i. e. ITS-IA and ITS-N type),and ITS-IA was the most popular type in the materials used in this study; the phylogeny analyzed results indicated that ITS-IA type and ITS-I type were distributed in different groups respectively,and the ITS-IA group appeared earlier than ITS-I group. Thus we proved that ITS-I type was evolved from a deletion of tRNA<sup>Ala</sup> coding region of ITS-IA type,and ITS-IA type should be the basic structure of ITS copy of <i>Phormidium</i>.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[JIAO Shu-Jing, HUANG Xian-En, GU Qing, SHI Quan-Liang<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>JIAO Shu-Jing, HUANG Xian-En, GU Qing, SHI Quan-Liang<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140303&flag=1]]></guid><cfi:id>12</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Apply <i>matK</i> gene to identify <i>Nervilia fordii</i> 
and its common adulterants]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140304&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In order to establish the novel method on distinguishing <i>Nervilia fordii</i> and its common adulterants,<i>matK</i> genes from <i>N. fordii </i>and its adulterants were amplified and sequenced using a pair of universal primes. The results revealed that <i>matK</i> genes acquired from <i>N. fordii</i> and its adulterants contained 587 base pairs,and average GC content was 32.8%. The intraspecific distances among <i>N. fordii</i> were 0,whereas the interspecific distance between <i>N. fordii </i>and its adulterants ranged from 0.016 to 0.375. The clustering tree according to Neighbor Joining method and Kimura 2-Parameter model discriminated <i>N. fordii</i> and its adulterants obviously. <i>matK</i> gene is suggested to be an effective biomarker to identify <i>N. fordii</i> and its common adulterants.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[HUANG Qiong-Lin, LIANG Ling-Ling, HE Rui, 
ZHAN Ruo-Ting, CHEN Wei-Wen<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HUANG Qiong-Lin, LIANG Ling-Ling, HE Rui, 
ZHAN Ruo-Ting, CHEN Wei-Wen<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140304&flag=1]]></guid><cfi:id>11</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Studies on the cell separation of the secondary xylem of 
pendulous characteristics of <i>Prunus mume</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140305&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Optical microscope was used to explore fiber morphology both in the upper and lower sides of one year-old branches among four upright and pendulous varieties by the H<sub>2</sub>O<sub>2</sub>-CH<sub>2</sub>COOH maceration. The results were as followed: the length of fiber in the lower side of the upright branches at the bottom was longer than the upper side significantly,the length of fiber in the upper side of the pendulous branches at the bottom was longer than the lower side significantly. There were no significant differences in other positions; the fiber diameter at different positions among four varieties indicated no significant differences separately.The results showed that the diferences of fiber size effects shoot development of <i>Prunus mume</i>.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[WANG Fu-Ting, YANG Wei-Ru, HAO Rui-Jie, WANG Tao, ZHANG Qi-Xiang<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Fu-Ting, YANG Wei-Ru, HAO Rui-Jie, WANG Tao, ZHANG Qi-Xiang<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140305&flag=1]]></guid><cfi:id>10</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Genetic diversity of leaves anatomical traits in different 
provenances of <i>Liriodendron chinense</i> seedlings]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140306&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Using the mature leaves of one-year old seedlings of five <i>Liriodendron chinense</i> provenances as materials,the 16 anatomical traits of leaf epidermis,leaf cross section and main vein cross section were observed and variance analyzed. The results showed that there were abundant variances in leaves anatomical traits among/within <i>L. chinense</i> provenances. Highly significant differences existed in all anatomical traits among/within provenances except the lower epidermis density among provenances. The mean phenotypic differentiation coefficient was 27.5%; this indicated the variation of main leaves anatomical traits within provenances(72.5%)was obviously higher than that of traits among provenances. The correlations among the anatomical features,geography and climate were also analyzed. The results indicated that the variations among provenances had the gradient regularity,and there were negative correlations between all epidermis traits and longitude and mean annual temperature. Most of traits of leaves and main vein cross section there were positive correlations with longitude and latitude,however,most of them had negative correlations with mean annual precipitation and mean annual temperature. According to the UPGMA cluster analysis based on the Euclidean distance,the five <i>L. chinense</i> provenances could be divided into three groups.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[ZHAO Li-Jun<sup>*</sup>, ZHU Li-Qiong, HUANG Shou-Xian, WEN Xiang-Feng]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHAO Li-Jun<sup>*</sup>, ZHU Li-Qiong, HUANG Shou-Xian, WEN Xiang-Feng</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140306&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[SCOT genetic diversity of plants in <i>Paris</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140307&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Gene resources and development prospects of plants in <i>Paris</i> were evaluated. Applied researches in genetic diversity of plant in <i>Paris</i> were carried out based on SCOT markers. Genomic DNA polymorphic analysis in total forty individuls of nine species in<i> Paris</i> were performed by the approach of start codon targeted polymorphism(SCOT). The genetic diversity of the nine species in<i> Paris</i> was high in Sichuan Province. Clustering analysis could be used to study the classification of <i>Paris</i>,which indicated that forty individuls were clustered 4 classes. <i>P. polyphylla </i>var.<i> stenophylla</i> was clustered alonely. <i>P. fargesii</i>,<i>P. delavayi</i> var. <i>petiolata</i>,<i>P. delavayi</i> var. <i>delavayi</i>,<i>P. polyphylla</i> var. <i>yunnaensis</i> were clustered. <i>P. thibetica</i> and <i>P. polyphylla</i> var. <i>chinesis</i> were clustered. <i>P. axiparis</i> var. <i>axialis</i> and <i>P. mairei</i> were clustered. In conclusion,plant in <i>Paris</i> was identified accuracily in molecular by SCOT markers and molecular evidences were provided on the taxonomic status of species and interspecific. It is helpful to further study on gene mapping of<i> P.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[LI Zhuang<sup>1</sup>, XIN Ben-Hua<sup>1</sup>, YANG Hua<sup>2</sup>, LIU Chen<sup>3</sup>, TIAN Meng-Liang<sup>3*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Zhuang<sup>1</sup>, XIN Ben-Hua<sup>1</sup>, YANG Hua<sup>2</sup>, LIU Chen<sup>3</sup>, TIAN Meng-Liang<sup>3*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140307&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[Genetic diversity of <i>Pinus crassicorticea</i> and its 
genetic relationship with two sympatric pine species]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140308&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Pinus crassicorticea</i> is a rare tree species has high economical value in northwestern Guangxi. As the habitat has been seriously damaged,<i>P. crassicorticea </i>is now regarded as an endangered species. To preserve the germplasm of this species,the genetic diversity of <i>P. crassicorticea</i> was quantified based on 7 SSR loci. The interspecies relationship between <i>P. crassicorticea</i> and two sympatric pine species,<i>P. yunnanensis </i>var. <i>tenuifolia</i> and <i>P. massoniana</i>,was further analyzed. The results showed that the mean number of effective alleles(<i>Ne</i>)per locus was 1.653,the average observed heterozygosity(<i>Ho</i>)was 0.577,the expected heterozygosity(<i>He</i>)was 0.374,Shannon's information index(<i>I</i>)was 0.540 and mean Nei's gene diversity(<i>h</i>)was 0.376,indicating that <i>P. crassicorticea</i> maintains high levels of genetic variation. The genetic identity(<i>GD</i>)was 0.0175 between <i>P. crassicorticea </i>and <i>P. massoniana</i>,while 0.0525 between <i>P. crassicorticea </i>and <i>P. yunnanensis </i>var. <i>tenuifolia</i>. The interspecies relationship coefficient was 0.094 within <i>P. crassicorticea</i> and <i>P. massoniana</i>,and 0.066 in <i>P. crassicorticea</i> and <i>P. yunnanensis</i> var. <i>tenuifolia</i>, respectively. Therefore,it was reasonable that <i>P. crassicorticea</i> was genetically closer to<i> P. massoniana</i> than <i>P. yunnanensis</i> var. <i>tenuifoli</i>. The strategy for the genetic resource conservation of <i>P. crassicorticea</i> was also discussed in this paper.]]></description>
<pubDate>2015/12/15 10:55:20</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[FENG Yuan-Heng<sup>1,2</sup>, WU Dong-Shan<sup>3</sup>, WANG De-Jun<sup>1</sup>, 
YANG Zhang-Qi<sup>2</sup>, LI Huo-Gen<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>FENG Yuan-Heng<sup>1,2</sup>, WU Dong-Shan<sup>3</sup>, WANG De-Jun<sup>1</sup>, 
YANG Zhang-Qi<sup>2</sup>, LI Huo-Gen<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140308&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[<i>Pellionia mollissima</i>, a new species of 
Urticaceae from Guangxi]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140101&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[A species of the genus <i>Pellionia</i>(Urticaceae),<i>P. mollissima</i>,is described as new from southwestern Guangxi. This species is characterized by its lineolate and tuberculate achenes,and by this unique fruit character it may be distinguished from all the other species of <i>Pellionia</i>.]]></description>
<pubDate>2015/12/15 10:10:33</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></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=20140101&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[Genetic diversity analysis with AFLP on fresh Chinese 
olive cultivars resources in Guangdong Province]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140102&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Screened from 64 pairs of the AFLP primer,six pairs(E/AAC-M/CAT,E/AAC-M/CTT,E/ACA-M/CAA,E/AGG-M/CAA,E/ACC-M/CAA,E/ACT-M/CAT),which produced clear and reliable polymorphic bands,were selected for analysis genetic relationship and genetic diversity among the 63 Chinese olive cultivars. 417 amplification bands were produced with 100% polymorphic rate. It was indicated that there was rich genetic diversity in Chinese olive cultivar germplasm. The genetic relationship of the 63 Chinese olive cultivars was analyzed with software NTSYSpc-2.10a,and a UPGMA tree was established. According to this tree,the Chinese olive cultivars in this studied could be divided into 7 cultivar groups with a similar coefficient 0.312,the Group 1 delegated by ‘Chaoyang sweet olive' including 45 cultivars,could be divided into 3 types,the Group 2 delegated by ‘Danatian' including 5 cultivars,the Group 3 delegated by ‘Chaoyang sanleng' including 4 cultivars,the Group 4 including 3 cultivars,the Group 5 including 2 cultivars,the Group 6 including 4 cultivars,and the Group 7 including one cultivar only,that was ‘Fenghu olive',which had a long distance in relationship with other cultivars,maybe occurred variation in cultivation practice.]]></description>
<pubDate>2015/12/15 10:10:33</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[ZHOU Jun-Hui<sup>1*</sup>, WANG Yan-Ping<sup>1,3</sup>, CHEN Qin<sup>2</sup>, ZHOU Zhi-Qin<sup>3</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHOU Jun-Hui<sup>1*</sup>, WANG Yan-Ping<sup>1,3</sup>, CHEN Qin<sup>2</sup>, ZHOU Zhi-Qin<sup>3</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140102&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[Analysis of genetic diversity of <i>Pinus yunnanensis </i>var. <i>
tenuifolia</i> nature populations by SSR marker]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140103&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[SSR markers were used to study genetic diversity of tree different nature populations of <i>Pinus yunnanensis </i>var. <i>tenuifolia</i>. The results showed that 13 sites and 37 alleles were detected. For every site,the average value of observation allele number(A)was 2.85,polymorphism rate was 100% and the average values of effective number of alleles(Ne)was 1.45. The average value of effective number of alleles was 1.447 within each population. <i>P. yunnanensis </i>var. <i>tenuifolia </i>had a low genetic diversity level among the three populations, the average observed heterozygosity(Ho)was 0.341 and the average expected gene heterozygosity(He)was 0.281. Nei's gene diversities(h)at population level were 0.256 and 0.297. Shannon's information indexes(I)at population level were 0.448 and 0.484. In addition, the three populations deviated from Hardy-Weinberge quilibrium. The average coefficient gene differentiation(Gst)was 0.089. Most of variation appeared inner population and there was not gene differentiations among populations. The range of gene flow of different gene polymorphism sites was 4.693-122.189,the average number was 11.17,which indicated that the habitat of <i>P. yunnanensis </i>var. <i>tenuifolia </i>was limited and resulted in the limited natural variation,but there were abundant gene exchanges between each population.]]></description>
<pubDate>2015/12/15 10:10:33</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[YANG Zhang-Qi<sup>1</sup>, FENG Yuan-Heng<sup>1</sup>, WU Dong-Shan<sup>2</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YANG Zhang-Qi<sup>1</sup>, FENG Yuan-Heng<sup>1</sup>, WU Dong-Shan<sup>2</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140103&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[Genetic diversity analysis of <i>Glehnia littoralis</i>
(Apiaceae)revealed by SRAP]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140104&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Sequence-related amplified polymorphism(SRAP)was used to analyze genetic relationships of eight populations of <i>Glehnia littoralis</i> F. Schmidt ex Miquel in China. Among them,seven populations were wild plants and one was cultivar plant. With eight SRAP primer combinations,168 loci were identified. Among them,118 were polymorphic and accounted for 70.23% of total amplified loci,showing a high polymorphism. The genetic similarity among these eight populations ranged from 0.830 6 to 0.983 6 and the genetic diversity was 0.0165-0.1856. Based on the results of cluster and principal coordinate analysis,the eight populations of <i>G. littoralis</i> were divided into three groups. The population from Dalian of Liaoling Province was confirmed as Group A, while populations from Shandong Province(excluding Rizhao)were clustered into Group B. Group C comprised populations from Rizhao of Shandong Province to Shenzhen,Guangzhou.]]></description>
<pubDate>2015/12/15 10:10:33</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[SONG Chun-Feng, LIU Qi-Xin<sup>*</sup>, ZHOU Yi-Feng, 
WU Bao-Cheng, DONG Xiao-Yu]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SONG Chun-Feng, LIU Qi-Xin<sup>*</sup>, ZHOU Yi-Feng, 
WU Bao-Cheng, DONG Xiao-Yu</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140104&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[Effects of shade on the leaf microstructure and 
chloroplast ultrastructure of the invasive <i>Wedelia 
trilobata</i>, the native <i>W. chinensis</i> and their hybrid]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140105&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The microstructure and the chloroplast ultrastructure of the primary fully expanded mature and senescent leaves of <i>Wedelia trilobata</i>,<i>W. chinensis</i> and their hybrid under shade and full light have been investigated using scanning electron microscope(SEM,JSM-6360LV)and transmission electron microscope(TEM,JEM-1010). In contrast to full light treatment,the primary fully expanded mature leaves of the three species under shade treatment had reduced stomatal density of both upper and lower epidermises,and smaller leaf thicknesses and thicknesses of upper and lower epidermises,palisade tissue and spongy tissue. Moreover,the chloroplast of the primary fully expanded mature leaves,the stacking of grana lamellae increased and the number of the starch grain increased. However,the effects of shade on the microstructure of the senescent leaves were different to that found in primary leaves. For hybrids,the thicknesses of the upper epidermis,the palisade tissue,the spongy tissue and the whole leaves increased. Also,the thickness of the lower epidermis of the invasive species(<i>W. trilobata</i>)and the thickness of the upper epidermis of the native species(<i>W. chinensis</i>)increased. Moreover,the ultrastructure of their chloroplasts had more severe impairment under shade treatment,e.g. the grana lamellae had edge-lysis. Conclusively,the response in leaf microstructure and chloroplast ultrastructure varied among different <i>Wedelia</i> species and different leaf developmental stages within the same species; the hybrid showed intermediate response between its parent species.]]></description>
<pubDate>2015/12/15 10:10:33</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[YI Li<sup>1,2</sup>, HU Xiao-Ying<sup>1</sup>, WEI Xiao<sup>3</sup>, YE Wan-Hui<sup>1</sup>, SHEN Hao<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YI Li<sup>1,2</sup>, HU Xiao-Ying<sup>1</sup>, WEI Xiao<sup>3</sup>, YE Wan-Hui<sup>1</sup>, SHEN Hao<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140105&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[Radical variation in growth ring width and tracheid 
dimensions of <i>Metasequoia glyptostrobides</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140106&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Radical variation in growth ring width and tracheid dimensions of <i>Metasequoia glyptostrobides</i> planted in Yaan,Sichuan were evaluated. The results were as follows:the growth ring width first increased from pith to 10-year old,then decreased,and the main wood formation period was 15 a. The tracheid length of late wood was longer than that of early wood,and the tracheid length increased with the growth age,then decreased after 13-year old. The determined values for tracheid width,cell wall thickness,and lumen diameter were 44.6,7.23,37.48 μm,respectively,and significant difference in these index were found between early and late wood. Length to width ration(L/W),cell wall thickness to lumen diameter(2T/D),and lumen diameter to width(L/W)was 95.40,0.27 and 0.82,respectively. The results obtained in this study indicated that <i>M. glyptostrobides</i> wood was available for pulping.]]></description>
<pubDate>2015/12/15 10:10:33</pubDate>
<category><![CDATA[Systematic Evolution and Biodiversity]]></category>
<author><![CDATA[QI Jin-Qiu, HAO Jian-Feng, XIE Jiu-Long, WU Bing-Ling, LUO Hao]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>QI Jin-Qiu, HAO Jian-Feng, XIE Jiu-Long, WU Bing-Ling, LUO Hao</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20140106&flag=1]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
</channel>
</rss>