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<title cf:type="text"><![CDATA[ -->Special Issue：Plant Classification and System Evolution]]></title>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Two new tetraploid quillwort species, <i>Iso&#235;tes longpingii</i> and <i>I. xiangfei</i> from China(Iso&#235;taceae)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221001&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Two new tetraploid quillwort species, <i>Iso&#235;tes longpingii</i> and <i>I. xiangfei</i>, from China are described and illustrated. <i>I. longpingii</i> is a fully submerged plant found in a small pond of Hunan Province. It is morphologically similar to<i> I. sinensis</i>, but differs in its small and tuberculate-cristate megaspores and soft slender leaves that grow up to 60 cm. It is also similar to hexaploid <i>I. orientalis</i>, but differs in its 44 chromosomes and tuberculate-cristate megaspores.<i> I. xiangfei </i>is most similar to diploid <i>I. yunguiensis</i> in megaspore ornamentation, but differs in its microspore ornamentation, oblong sporangium, and 44 number of chromosomes. There are a few individuals of <i>I. longpingii</i> found in Ningxiang City of Hunan Province, and <i>I. xiangfei</i> is distributed in the wetlands of Tongdao and Huitong counties of Hunan Province. Because of their limited geographic ranges, small populations, fewer individuals and disturbed habitats, <i>I. longpingii</i> and <i>I. xiangfei</i> are evaluated as critically endangered(CR)and vulnerable(VU)category, respectively, according to the IUCN Red List criteria. A key to all the current known Chinese quillworts is also provided for further taxonomic identification and conservation of these rare and endangered plants in China.]]></description>
<pubDate>2022/11/9 0:00:00</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[SHU Jiangping<sup>1, 2</sup>, GU Yufeng<sup>1, 3</sup>, OU Zhiguo<sup>4</sup>, SHAO Wen<sup>5</sup>, YANG Juan<sup>6</sup>, LU Qiyong<sup>6</sup>, 
ZHANG Xianchun<sup>7</sup>, LIU Baodong<sup>3</sup>, WANG Ruijiang<sup>2*</sup>, YAN Yuehong<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SHU Jiangping<sup>1, 2</sup>, GU Yufeng<sup>1, 3</sup>, OU Zhiguo<sup>4</sup>, SHAO Wen<sup>5</sup>, YANG Juan<sup>6</sup>, LU Qiyong<sup>6</sup>, 
ZHANG Xianchun<sup>7</sup>, LIU Baodong<sup>3</sup>, WANG Ruijiang<sup>2*</sup>, YAN Yuehong<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221001&flag=1]]></guid><cfi:id>38</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>Selaginella pseudotamariscina </i>(Selaginellaceae), an 
overlooked rosette-forming resurrection 
spikemoss from Vietnam]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221002&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[A new species, <i>Selaginella pseudotamariscina</i> X. C. Zhang &amp; C. W. Chen(Selaginellaceae), is described from Vietnam. The placement of this species within <i>Selaginella</i> subg. <i>Stachygynandrum</i> is assessed based on molecular phylogenetic analyses and morphological comparisons with related species. Molecular phylogenetic analyses suggest that <i>S. pseudotamariscina</i> is sister to <i>S. digitata</i>-<i>S. imbricata</i> clade. Morphologically, the new species is similar to <i>S. tamariscina</i> and <i>S. pulvinata</i> by sharing the rosette-forming habit, but distinguished by its dorsal leaves symmetrical, lanceate, sulcate on upper surface; strobili slightly dorsiventrally complanate and non-resupinate, sporophylls resembling vegetative leaves in form and arrangement, non-resupinate, the ventral sporophylls larger than the dorsal ones, dorsal sporophylls sterile, sporangia only borne on the base of ventral sporophylls.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHANG Menghua<sup>1,2</sup>, YANG Jie<sup>1,2</sup>, LUU Hong Truong<sup>3</sup>, TRAN Gioi<sup>3</sup>, ZHANG Xianchun<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Menghua<sup>1,2</sup>, YANG Jie<sup>1,2</sup>, LUU Hong Truong<sup>3</sup>, TRAN Gioi<sup>3</sup>, ZHANG Xianchun<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221002&flag=1]]></guid><cfi:id>37</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Supplementary description of flowering branches and 
flowers of <i>Bonia amplexicaulis</i> in Guangxi]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221003&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Reproductive organs are of great significance in taxonomic studies of bamboo plants. In this paper, Latin and Chinese supplementary descriptions are provided for flowering branches and reproductive organs characteristics of bamboo species <i>Bonia amplexicaulis</i> distributed according to observed flowering condition and anatomical observation results of the collected specimens in Mashan County, Guangxi. By comparing the floral characteristics of the reproductive organ structures of <i>Bonia</i> species <i>B. saxatilis</i>, <i>B. parvifloscula </i>and <i>B. amplexicaulis</i>, the three species have the same reproductive organ structure characteristics, but there are differences in the number and size of florets. The comparison of reproductive organs shows that the reproductive organs of <i>Bonia</i> species have special adaptability to karst geomorphic environment, supports that they are independent species according to the differences of nutritive organs.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHANG Yuqu, YANG Xinjie, CHENG Huyin, GAO Jing, 
PENG Liang, ZHANG Mingying, ZHANG Gang<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Yuqu, YANG Xinjie, CHENG Huyin, GAO Jing, 
PENG Liang, ZHANG Mingying, ZHANG Gang<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221003&flag=1]]></guid><cfi:id>36</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Exclusion of <i>Glochidion arborescens</i> 
(Phyllanthaceae)from the flora of China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221004&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The species <i>Glochidion arborescens</i> Blume has long been considered to be widely distributed in Yunnan Province, China. Based on years of extensive specimen examinations and field investigations, we demonstrated that all the Chinese specimens previously identified as <i>G. arborescens</i> mostly belonged to <i>G. heyneanum</i>(Wight &amp; Arn.)Wight, while several others belonged to <i>G. acuminatum </i>var. <i>acuminatum</i> M&#252;ll. Arg., <i>G. eriocarpum</i> Champ. ex Benth., <i>G. lancolarium</i>(Roxb.)Voigt or <i>G. zeylanicum</i> var. <i>tomentosum</i>(Dalzell)Trimen. <i>G. arborescens</i> is not found to China and thus the distribution of the species in China is excluded. In addition, a lectotype of <i>G. arborescens</i> is specified, and a species key of <i>G. arborescens</i> and relevant misidentified species is provided.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHANG Wenhua<sup>1</sup>, GUO Yongjie<sup>2, 3</sup>, LI Yuling<sup>1</sup>, YAO Gang<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Wenhua<sup>1</sup>, GUO Yongjie<sup>2, 3</sup>, LI Yuling<sup>1</sup>, YAO Gang<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221004&flag=1]]></guid><cfi:id>35</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Morphological and cytological studies on 
male sterility in <i>Ferula sinkiangensis</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221005&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Ferula sinkiangensis</i> is a perennial herb, producing fruits only once through its life history, and exclusively habitated in Xinjiang being in the list of state rare and endangered plants Level 2. Besides andromonoecy, usually found in Umbelliferae, plants of male sterility were observed in their populations. Aimed to male sterility and the factors inducing it, comparative observation on morphology of male sterility individuals and functional female flowers were executed through field investigation, and study on cytology of the process of the anther degeneration in female flowers were made from paraffin sections. The results were as follows:(1)Female plants germinated at the end of March and blossomed in the middle of April, and their fruits matured at the end of May; Phenological phases of them were the same as those of andromonoecy.(2)The average height and diameter of plant, and number of the first level branch of female individuals were(71.00&#177;10.92)cm,(71.67&#177;17.64)cm, and(23.83&#177;2.04), separately; The average length and width of basal leaves were(33.41&#177;11.63)cm and(24.47&#177;8.60)cm; The female and the andromonoecy were the same in size of both the plant and the leaf.(3)On female plants, inflorescences on the first and the second level branches were all female, which could bear fruits wholly; The number of umbels in the inflorescence(13.22&#177;4.70)and number of flowers in the umbel(12.03&#177;2.30)and number of total flowers in the inflorescence(159.08)were higher than those in individuals of hermaphrodite; Female plants produced more flowers which could set fruits and bore out-crossing seeds of heterosis.(4)In female umbels flowers located tightly and the distance among flowers were shorter than those in both hermaphrodite and male umbels; Female flowers opened slightly in the whole flowering stage, while petals of both hermaphrodite and male flowers folded reversely.(5)There were no differences in morphological characteristics of petals and pistils among different sexual flowers. But the length(1.79&#177;0.39 mm)and width(1.10&#177;0.21 mm)of petals, and the length of stamens(0.6-1.3 mm)in the functional female flower were the smallest, where anthers degenerated and no pollen stain well developed.(6)Abnormal development of the anther on the degenerated stamen appeared in both of parietal cells and male gametophytes from sporogenous cell stage to microspore tetrad stage. In conclusion, the nutrients productivity in plants of male sterility is similar as andromonoecy, but patterns of resource distribution are quite different; there are significant differences between female and hermaphrodite/male flowers in both the morphology and the function; abnormal development of parietal cells, especially because of the lack of tapetum, caused abortion of microspores in the functional female flower.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[HE Shuang<sup>1*</sup>, TAN Dunyan<sup>2,3,4</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HE Shuang<sup>1*</sup>, TAN Dunyan<sup>2,3,4</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221005&flag=1]]></guid><cfi:id>34</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Leaf morphology and taxonomic significance of 
five species in Hypoxidaceae from China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221006&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In order to provide new data for clarification of the generic relationship in Hypoxidacae, morphology, ultrastructure, and anatomy of leaf from five species in this family were investigated using microscope, scanning electronic microscope(SEM), and paraffin section. It turned out that there were five points of views as below:(1)Three types of leaf shapes were characterized, including small-even, middle-wave, and large-plicate.(2)Trichomes were single-celled and uniseriate, and grouped into pilose, strigose and stellate types.(3)Shapes of leaf epidermal cells were hexagon and pentagon, while stomata was paracytic and elliptic with a negative correlation between size and density.(4)Sculptures of wax in epidermis was classified into smooth, granular, scales and crust types.(5)Leaf anatomy revealed two types of vascular bundles, leaf transection of midrib had flat and carinate types, and its shape was divided into round and oblong, with relevance between thickness of epidermis and size of epidermal cells. Based on comparative morphology and anatomy of leaf, it is suggested that complex of some characteristics would be helpful for understanding of generic relationships in <i>Hypoxis</i>, <i>Curculigo</i> and <i>Molineria</i>, while other characteristics for species identifications. In addition, <i>Molineria</i> should be regarded as an independent genus from <i>Curculigo sensu lato</i>.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[TIAN Qin<sup>1,2</sup>, DUAN Hanning<sup>1</sup>, WANG Yunqiang<sup>3</sup>, LI Haitao<sup>3</sup>, LI Lu<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>TIAN Qin<sup>1,2</sup>, DUAN Hanning<sup>1</sup>, WANG Yunqiang<sup>3</sup>, LI Haitao<sup>3</sup>, LI Lu<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221006&flag=1]]></guid><cfi:id>33</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 and its taxonomic significance of 
10 <i>Primula </i>species from the Shergyla Mountains]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221007&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Primula</i> is an important genus of Primulaceae, which has high ornamental value because of diverse flower colors and long flowering period. In order to provide palynology basis for the taxonomy of this genus, we observed and compared the pollen morphological characteristics of 10 <i>Primula </i>species from the Shergyla Mountains in Tibet by scanning electron microscopy(SEM). Moreover, clustering analysis was carried out on the basis of these characteristics of pollen morphology. The results were as follows:(1)Pollen shapes of 10 <i>Primula </i>species varied from oblate to nearly spherical. Among these species, the pollen of <i>P. calderiana </i>was the biggest, and the smallest was that of <i>P. kongboensis</i>. The germinal aperture of <i>P. tibetica </i>was stephanocolpate type. The other pollens usually were tricolporate type, most of the colpus converged to form parasynocolpus in the polar region.(2)The pollen exine ornamentation were mostly foveolate or reticulate, which of <i>P. chungensis </i>and <i>P. tibetica </i>were coarsely reticulate.(3)In traditional classification, 10 species belong to 7 sections respectively. Clustering analysis based on pollen characteristics showed a certain level of consistency with the traditional classification. However, <i>P. tibetica </i>and <i>P. kongboensis</i>, both belonging to Sect. <i>Aleuritia</i>, maintained a relatively distant relationship due to their obvious differences in pollen traits. The preliminary results show that there are interspecific differences in the pollen morphology of 10 <i>Primula</i> species, which can provide a certain degree of reference for classification of plants. But it should be reminded that in addition to pollen characteristics, morphology and molecular biology still need to be comprehensively considered in classification.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[LIU Lin, ZHANG Liangying<sup>*</sup>, CHENG Guilan, HE Dan, ZHANG Lifei, MENG Fanli]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIU Lin, ZHANG Liangying<sup>*</sup>, CHENG Guilan, HE Dan, ZHANG Lifei, MENG Fanli</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221007&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[Timescale of angiosperm evolution based on Ks distribution]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221008&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Estimating the time scale of species evolution is an important part of life evolution study. It is found that there are significant differences in the evolution rates of different genes and species in recent years, which challenges the molecular clock hypothesis to a great extent. Therefore, new methods are needed to re-estimate the evolutionary event time. The whole genome sequence of angiosperms makes it possible to estimate the evolutionary time from the whole genome perspective. In order to re-estimate the evolution time of angiosperms, an evolution rate correction model based on genomic data is established according to the idea that shared polyploidy events or shared divergence events should have the same Ks peak. The results were as follows:(1)Three common ways to obtain Ks distribution were compared and analyzed, which showed that the best way was to extract the median of Ks values on collinear blocks.(2)The change process of Ks distribution was simulated with time accumulation coefficient(<i>v</i>)of Ks values. When v was assumed to obey the normal distribution, the Ks distribution had a long tail phenomenon.(3)The correction process was described in detail, which was conducive to the understanding and wide spread of this method. From the application of correction method in angiosperms, it was found that the Ks peak before correction was not linear with time, while the Ks peak after correction was directly proportional to time, indicating that it is very necessary to estimate the time of species evolution events after correcting the Ks peak. It was also found that although the evolution rate of angiosperms was significantly different, the evolution rate between different branches was still partially consistent. For example, Magnoliids had the slowest evolutionary rate, followed by Eudicots and Monocots. When the environment changed greatly, most species of different lineages of angiosperms had synchronous radial evolution and adaptive evolution. Finally, a relatively reliable angiosperm evolution time axis was establish, which helps to understand the evolution process and model, especially to understand the phylogenetic relationship and the causes of diversity and provides phylogenetic and evolutionary support for plant research.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[JIAO Beibei, WANG Xiyin<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>JIAO Beibei, WANG Xiyin<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221008&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[Phylogenetic diversity and its distribution pattern of 
asterids in Yunnan angiosperms flora]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221009&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Biodiversity conservation has attracted much attention around the world due to species extinction risks resulting from global climate change, human activities and so on. Traditional attempts to biodiversity conservation typically focus on the analyses of taxonomic composition and its distribution pattern of species, endemic species and threatened species, and ignore the rich context that evolutionary history can provide. As the intersection area of global biodiversity hotspots, the biodiversity conservation in Yunnan has been widely concerned. To better protect biodiversity in Yunnan, we combine data on the distributions and phylogenetic relationships of species from asterides in Yunnan angiosperms flora, explore how taxonomic composition(including species, endemic species and threatened species)and phylogenetic diversity vary across the different geographic regions in this area. And then integrating the distribution of nature protected areas with data of taxonomic and phylogenetic composition, we identify the key areas for biodiversity conservation. The results were as follows: Phylogenetic diversity was well correlated with taxonomic richness for species, endemic species and threatened species among the geographic regions; Using null model analyses, we found the standardized effect size of the phylogenetic diversity decreased gradually in Yunnan from south to north; We suggest that the southern, southeastern and northwestern Yunnan should be the biodiversity priority areas since they may help maximize the protection of evolutionary history and potential for Yunnan angiosperm flora. It can been seen that the integration of phylogenetic information can help us to better understand the formation and development of plant diversity, and provide more clues for the formulation of biodiversity protection strategies.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHOU Hanjie<sup>1,2</sup>, YANG Ruxuan<sup>1,2</sup>, LI Rong<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHOU Hanjie<sup>1,2</sup>, YANG Ruxuan<sup>1,2</sup>, LI Rong<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221009&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[Genealogical structure and differentiation analysis of 
<i>Carpinus tientaiensis</i> based on single nucleotide 
polymorphism of chloroplast genome]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221010&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Carpinus tientaiensis</i> is an endangered plant species with sparse population densities and is endemic to China. The distribution of this species is restricted to the territory of Zhejiang Province and its survival rate is very low. Based on data of chloroplast genome(cpDNA)single nucleotide polymorphism(SNP)in six natural populations(including the mother plants of all populations), we investigated genealogical structure and systematic development, assessed how endangered <i>C. tientaiensis</i> is and put forward relevant conservation strategies. The genomic DNA of <i>C. tientaiensis</i> was extracted using TIANGEN kit method and a library was constructed for high-throughput sequencing with Illumina NovaSeq 6000. To obtain the sequence of chloroplast complete genome, cpDNA maps were constructed using the online program OGDRAW. Nucleotide diversity was analyzed by DnaSP software while PopART was used for haploid network construction and RAxML was adopted for maximum likelihood(ML)tree construction. Finally, MrBayes software was used for construction of Bayes tree. The results were as follows:(1)According to chloroplast complete genome sequence analysis of <i>C. tientaiensis</i>, most of the protein-coding genes and amino acid sequences showed obvious codon preference. Moreover, chloroplast long-term relationship(cpLTR)revealed 32 forward repeats, 25 palindromic repeats and 22 reverse repeats. We detected 87 simple sequence repeats(SSR)in different types, most of which were A/T rich and the number of single nucleotides was the largest.(2)A total of 314 SNPs was identified in the cpDNA of <i>C. tientaiensis</i>. Single-nucleotide substitution indicated that <i>C. tientaiensis</i> was monophyletic and could be categorized into Tiantai County(THS)and Jingning County(JST)populations. The evolution of the haplotypes of the population manifested stellar radiation.(3)The variation of nucleotide diversity was low in all populations(<i>P<sub>i</sub></i>&lt;0.005)and the haplotype diversity of THS and JST populations was also low(<i>H<sub>d</sub></i> 0.5-0.6). This indicated that <i>C. tientaiensis</i> had undergone historically local expansions after experiencing bottlenecks across its evolution history, with lower genetic variation within populations and higher level of diversity among populations. The results of SNP of the cpDNA reveal the genetic diversity and lineage differentiation of <i>C. tientaiensis,</i> and provide theoretical basis for conservation of the genetic resources as well as rescue of this endangered plant species.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[CHEN Moshun, YANG Zhongyi]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CHEN Moshun, YANG Zhongyi</atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221010&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[Confirmation of the systematic positions about 
<i>Biondia</i> and <i>Merrillanthus</i>(Apocynaceae)
based on molecular evidence]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221011&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Biondia </i>Schltr., containing about 13 species, is endemic to China, and <i>Merrillanthus</i> Chun &amp; Tsiang is a monotypic genus distributing only in China and Cambodia. These two genera have been included in <i>Vincetoxicum</i> Wolf, but their phylogenetic positions and taxonomic status need further study because of insufficient samples and phylogenetic analysis. We reconstructed the phylogenetic trees of Tylophorinae based on two ribosomal gene sequence data(ITS, ETS)and five chloroplast gene sequence data(<i>psbA-trnH</i>, <i>trnG</i>, <i>trnL</i>, <i>trnL-F</i>, <i>trnT-L</i>)individually and combined data, which contained two types of species samples [including <i>B. chinensis</i> Schltr.=<i>V. shaanxiense</i>(Schltr.)Meve &amp; Liede and <i>M. hainanensis</i> Chun &amp; Tsiang=<i>V. hainanense</i>(Chun &amp; Tsiang)Meve, H. H. Kong &amp; Liede]. The results showed that<i> Biondia </i>and <i>Merrillanthus </i>were nested inside the <i>Vincetoxicum</i>; the type species <i>B. chinensis</i> Schltr.=<i>V. shaanxiense</i>(Schltr.)Meve &amp; Liede were sister to <i>B. henryi</i>(Warb.)Tsiang &amp; Li=<i>V. henryi</i>(Warb.)Meve &amp; Liede, and formed a clade with <i>V. kawaroense</i> Meve &amp; Liede; while <i>B. insignis</i> Tsiang=<i>V. insigne</i>(Tsiang)Meve,H. H. Kong &amp; Liede belonged to the Subtropical Clade; <i>Merrillanthus </i>formed a clade with <i>V. cissoides</i>(Blume)Kuntze and <i>V. philippicum</i> Meve, Omlor &amp; Liede. Our results support that <i>Biondia </i>and<i> Merrillanthus</i> should be included in <i>Vincetoxicum</i>, but<i> Biondia </i>is polyphyletic, more species samples and data need to be collected and analysed to further explore their phylogenetic positions about <i>Vincetoxicum.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[LIAO Miao<sup>1</sup>, ZENG Sijin<sup>2</sup>, TANG Guangda<sup>1,3*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIAO Miao<sup>1</sup>, ZENG Sijin<sup>2</sup>, TANG Guangda<sup>1,3*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221011&flag=1]]></guid><cfi:id>28</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Influence of net diversification rate and evolutionary 
time on the differences in species richness among 
families of order Saxifragales]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221012&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The differences in the species richness among different biological taxonomic groups often vary greatly, which is a phenomenon commonly observed in ecological and biological studies. However, the underlying mechanisms of this pattern are still in hot debate. From the perspective of macroevolution, time-for speciation hypothesis and diversification rate hypothesis are two popular hypotheses. Time-for speciation hypothesis suggesting that the time-for-speciation is the primary driver of diversity variation among groups by species accumulation along time, while diversification rate hypothesis suggesting that the groups with high species number resulted from their high net diversification rates. To test these two hypotheses, we studied species variation among 15 families of order Saxifragales based on a fossil-calibrated phylogenetic tree containing 1 539 species. We obtained the rates of speciation and extinction of 15 families and calculated the average diversification rate of each family through macroevolutionary analysis. The results are as follows:(1)The species diversification rate of order Saxifragales shows an increasing trend, and the increase of diversification rate mainly occurred in temperate and alpine groups, such as Grossulariaceae, Crassulaceae and Paeoniaceae.(2)The results of phylogenetic generalized least squares(PGLS)and linear regression model(LM)show that the species richness of the 15 families is not significantly correlated with the age of family differentiation or the age of the most recent common ancestor, but it is positively correlated with the net diversification rate(<i>R</i><sup>2</sup>=0.380, <i>P</i>&lt;0.05). These results support the diversification rate hypothesis, suggesting that the diversification rate is a primary evolutionary driver of the variation of species richness among families of order Saxifragales. Global cooling may provide opportunities for the expansion of distribution and rapid species diversification of herbaceous, deciduous trees and shrubs those can adapt to cold conditions. The study show that in temperate and alpine spreading groups, the net diversification rate may be the main reason for the differences in species numbers of different taxonomic groups.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[GU Jiahao<sup>1,2</sup>, ZHANG Lihao<sup>1,2</sup>, ZHANG Haoyu<sup>1,2</sup>, WU Tianqing<sup>1</sup>, HUANG Linqing<sup>3</sup>, 
CHENG Ruijing<sup>1,2</sup>, XU Ying<sup>1,2</sup>, WANG Qinggang<sup>4</sup>, XU Xiaoting<sup>1,2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>GU Jiahao<sup>1,2</sup>, ZHANG Lihao<sup>1,2</sup>, ZHANG Haoyu<sup>1,2</sup>, WU Tianqing<sup>1</sup>, HUANG Linqing<sup>3</sup>, 
CHENG Ruijing<sup>1,2</sup>, XU Ying<sup>1,2</sup>, WANG Qinggang<sup>4</sup>, XU Xiaoting<sup>1,2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221012&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[Plastid phylogenomic insights into the 
phylogeny of Convolvulaceae]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221013&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Convolvulaceae is a cosmopolitan family with rich morphological characteristics and important economic values. However, the phylogenetic relationships among the major branches or tribes in the family have not been fully resolved. In order to resolve these relationships, we sampled the complete plastome sequences from 40 species, representing eight tribes of Convolvulaceae, and reconstructed phylogenetic trees by using both maximum likelihood and Bayesian inference approaches. The results were as follows:(1)Convolvulaceae plastomes had the typical quadripartite structure, with the plastome size ranging from 113 273 to 164 112 bp and including 66-79 protein-coding genes.(2)Phylogenomic analyses using five DNA matrixes(i.e., WCG, CDS, LSC, IR, and SSC)showed that the topologies of the WCG and CDS trees were basically the same, with slight differences in support values for some branches. Topological differences were found between LSC and WCG topologies, especially for the positions of Cuscuteae, Dichondreae and Cresseae. The AU and SH tests showed that topological conflicts were significant between the WCG matrix and the SSC and IR matrixes.(3)All phylogenetic analyses confirmed that <i>Cuscuta</i> and Dichondreae were nested in Convolvuloideae and should be treated as tribes.(4)Phylogenetic relationships among the eight tribes were well resolved using the WCG and CDS matrixes: Cardiochlamyeae and Erycibeae formed a clade as the first divergent group of Convolvuloideae, followed by Cuscuteae, with the remaining five tribes forming two major clades.(5)The phylogenomic analyses confirmed that Merremieae were polyphyletic, especially <i>Merremia</i>, and that the circumscription and taxonomy of both Merremieae and <i>Merremia</i> will need revision.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[CHEN Liqiong<sup>1,2</sup>, ZHANG Zhirong<sup>3</sup>, YANG Junbo<sup>3</sup>, LI Dezhu<sup>3</sup>, YU Wenbin<sup>1,4,5*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CHEN Liqiong<sup>1,2</sup>, ZHANG Zhirong<sup>3</sup>, YANG Junbo<sup>3</sup>, LI Dezhu<sup>3</sup>, YU Wenbin<sup>1,4,5*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221013&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[Analysis of complete chloroplast genome characteristics 
from wild populations of <i>Acanthocalyx alba</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221014&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Acanthocalyx alba</i> is a common medicinal plant in Tibetan of China, and there are few reports on its whole chloroplast genome now. In order to reveal basic characteristics of the whole chloroplast genome of <i>A. alba</i> and explore its phylogeographic structure, ten individuals from five wild populations were sequenced by Illumina sequencing platform. After assembly and annotation, ten complete chloroplast genome sequences were obtained. Moreover, genome characteristics and phylogenetic relationships were explored. The results were as follows:(1)The complete chloroplast genomes of <i>A. alba</i> were 155 335-156 266 bp. A total of 113 genes were annotated, including 72 protein-coding genes, 30 tRNA genes and four rRNA genes. The chloroplast genome was highly conserved in species in terms of size, structure, GC content and gene composition.(2)Genomic comparative analysis showed that the fragments with large variation were located in the single copy region, and there was no obvious expansion and contraction at the IR boundaries.(3)Analysis of population genetics revealed rich genetic diversity in the wild populations and significant geographic structure, and there were certain relationships between genetic distances and geographic distances. This study lays the foundation for studies on population genetics and phylogenomics of species in <i>Acanthocalyx</i>.]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHANG Qian<sup>1</sup>, ZHANG Dequan<sup>1,2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Qian<sup>1</sup>, ZHANG Dequan<sup>1,2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221014&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[New records of species <i>Carcinomyces polyporina </i>
andgenus<i> Carcinomyces </i>in China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221015&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[This study reported a macrofungus specimen with special morphology collected from Liancheng National Nature Reserve in Gansu Province. Morphological characteristics observation and molecular phylogenetic analysis based on ITS sequences were performed. The results show that the specimen is <i>Carcinomyces polyporina</i>, belonging to Basidiomycota, Tremellomycetes, Tremellales, Carcinomycetaceae, which represents a newly recorded genus and species in China, and is the first report of this genus in East Asia. <i>Carcinomyces polyporina</i> is characterized by parasitism on polypores fruitbody, forming gelatinous mycocecidium, basidia with longitudinally septate, and conidia commonly gemmated from basidiospores germination. The specimen is deposited in the Herbarium of Cryptoflora, Kunming Institute of Botany, Chinese Academy of Sciences(HKAS 115765).]]></description>
<pubDate>2022/11/9 16:47:41</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHU Xuetai<sup>1*</sup>, DU Fan<sup>1</sup>, YE Xiaoyan<sup>2</sup>, FAN Jiaxin<sup>1</sup>, JIANG Changsheng<sup>3</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHU Xuetai<sup>1*</sup>, DU Fan<sup>1</sup>, YE Xiaoyan<sup>2</sup>, FAN Jiaxin<sup>1</sup>, JIANG Changsheng<sup>3</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221015&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[<i>Opuntia humifusa </i>(Raf.)Raf., a newly naturalized 
species of Cactaceae in China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221016&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Opuntia humifusa </i>(Raf.)Raf.(Cactaceae), a newly recorded species in China, was discovered during a survey of succulent resources. This species is distinct from other <i>Opuntia</i> species distributed in China, with the dark green prostrate cladodes, no glaucous, spines absent, and bright yellow flowers. <i>O. humifusa</i> is one of the few hardy species in the family Cactaceae. It is native to North America and has been recently naturalized in Wulian County, Rizhao City, Shandong Province, China. It is the northernmost wild cactus found in China. This species might have been introduced and planted during the national promotion of Chinese herbal medicine in the 1950s, and gradually spreaded through human activities. Here we clarify the taxonomic problems of <i>O. humifusa</i> and <i>O. cespitosa</i> in Jiangsu Province, and deliver perspective views for future reasonable development and utilization of <i>O. humifusa</i> in the warm temperate zone of China.]]></description>
<pubDate>2022/11/9 16:47:42</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[WANG Qi, YAN Jing<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Qi, YAN Jing<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221016&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[Additions to <i>Goniothalamus</i>(Annonaceae)
in the flora of China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221017&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Goniothalamus sesquipedalis</i>(Colebr. ex Wall.)Hook. f. &amp; Thomson and <i>G. peduncularis </i>King &amp; Prain are reported as two new records for the flora of China, the two species were found in Yingjiang County, Yunnan Province, China and conserved in Xishuangbanna Tropical Botanical Garden. <i>G. lii</i> X.L. Hou &amp; Y.M. Shui has been treated as synonym with <i>G. yunnanensis</i> W. T. Wang in <i>Flora of China</i>. Here, we clarified its taxonomical status and treated as a new synonym with <i>G. peduncularis </i>based on living plants observation, the type specimens and the literatures revision. <i>G. sesquipedalis</i> was previously known from India, Bangladesh and Myanmar, and <i>G. peduncularis</i> was only in Myanmar. In this paper, we update the description and illustrate them based on the herbarium specimens and living collections. The voucher specimens are deposited in the Herbarium of Xishuangbanna Tropical Botanical Garden(HITBC).]]></description>
<pubDate>2022/11/9 16:47:42</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[YANG Bin<sup>1,2,3</sup>, WANG Liyan<sup>4</sup>, ZHOU Shishun<sup>1</sup>, LI Jianwu<sup>1</sup>, 
XIAO Chunfen<sup>5</sup>, TAN Yunhong<sup>1,3*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YANG Bin<sup>1,2,3</sup>, WANG Liyan<sup>4</sup>, ZHOU Shishun<sup>1</sup>, LI Jianwu<sup>1</sup>, 
XIAO Chunfen<sup>5</sup>, TAN Yunhong<sup>1,3*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221017&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[Newly recorded species data of Orchidaceae]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221018&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The Eastern Himalayan region is a hotspot of biodiversity in the world, and Tibet of China is an important region of it. It is of great significance to clarify the background plant resources and geographical distribution in this region for the study of regional flora. Five newly recorded genera, namely <i>Callostylis </i>Blume, <i>Chiloschista </i>Lindl., <i>Diploprora </i>Hook. f<i>.</i>, <i>Taeniophyllum</i> Blume and <i>Yoania</i> Maxim., are reported from Tibet Autonomous Region, China. The five newly recorded species are <i>Callostylis rigida </i>Bl., <i>Chiloschista yunnanensis</i> Schlechter, <i>Diploprora championii </i>(Lindl.)Hook. f<i>.</i>, <i>Taeniophyllum retrospiculatum </i>King &amp; Pantl. and <i>Yoania prainii </i>King &amp; Pantl. Morphological descriptions and characteristic pictures of the newly recorded genera and species are also attached. The results of this study further enrich the flora data of China, broaden the records of orchids in Tibet, and have important value for the diversity and conservation of orchids in Tibet and adjacent areas.]]></description>
<pubDate>2022/11/9 16:47:42</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[LI Mengkai<sup>1</sup>, Pubu Dunzhu<sup>2</sup>, XING Zhen<sup>1</sup>, LI Huiling<sup>3</sup>, ZHANG Zhang<sup>3</sup>, WANG Wei<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Mengkai<sup>1</sup>, Pubu Dunzhu<sup>2</sup>, XING Zhen<sup>1</sup>, LI Huiling<sup>3</sup>, ZHANG Zhang<sup>3</sup>, WANG Wei<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221018&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[from Tibet, China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221019&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>College of Forestry, Southwest Forestry University</i>, Kunming 650224, China]]></description>
<pubDate>2022/11/9 16:47:42</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHANG Xu, ZHOU Haiyi, XU Changlong, XU Bo<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Xu, ZHOU Haiyi, XU Changlong, XU Bo<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221019&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[<i>Cymbella pavanaensis</i> A. Vigneshwaran et al., 
a diatom reported for the first time in China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221020&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[During the process of studying the diatom diversity of Hunan Province, we find that a <i>Cymbella</i> species collected from Xiang River possesses the following diagnostic features:(1)Cells are small and their lengths are less than 29 μm;(2)Valves exhibit slight dorsiventrality;(3)Distal raphe fissures are dorsally deflected;(4)Apical pore fields are very small and composed of 1-3 transapical rows of porelli, which comprise two forms, one is slit-like, similar to the areolae on the valve face, and the other is rounded with internal openings covered by the flap-like silica projections;(5)Striae 10-12/10 μm at the dorsal middle part, 11-13/10 μm at the ventral middle part, and areolae 30-40/10 μm;(6)And 1-2 stigmata exist near the valve ventral central area. After comparing this species with the type population of <i>Cymbella pavanaensis</i> A. Vigneshwaran et al., in this paper, it is identified as <i>C. pavanaensis</i>. This paper provides a clearer knowledge of the ultrastructure of <i>C. pavanaensis</i>, enlarges its geographical distribution region, and reports it for the first time in China.]]></description>
<pubDate>2022/11/9 16:47:42</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[LONG Jiyan<sup>1</sup>, LIU Bing<sup>1*</sup>, ZHOU Yangyan<sup>1</sup>, XU Sanmei<sup>1, 2</sup>, CHEN Jinhua<sup>1</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LONG Jiyan<sup>1</sup>, LIU Bing<sup>1*</sup>, ZHOU Yangyan<sup>1</sup>, XU Sanmei<sup>1, 2</sup>, CHEN Jinhua<sup>1</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=221020&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[<i>Boehmeria nivea</i> var. <i> strigosa</i>(Urticaceae), 
a new variety from Southwest China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240901&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Boehmeria nivea</i> var. <i>strigosa</i> Zeng Y. Wu &amp; Y. Zhao, a new variety of <i>B. nivea</i>(Urticaceae)from Southwest China, is here described based on evidence from morphology and molecular phylogeny. This new variety is mainly characterized by its green abaxial leaf blade, partly connate stipules, and densely patent strigose hairs on stems and potioles. The phylogenetic analysis based on <i>rbc</i>L, nrDNA and <i>rbc</i>L+nrDNA datasets, revealed that all individuals of <i>B. nivea</i> var. <i>strigosa</i> formed a monophyletic group. The conservation status of <i>B. nivea</i> var. <i>strigosa </i>is assessed as “Near Threatened”(NT)according to IUCN evaluation criteria. The discovery of this new variety is not only crucial for the taxonomy of ramie, but also provides reference for the exploration and utilization of ramie.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHAO Ying<sup>1,4</sup>, Richard I. MILNE<sup>5</sup>, LI Zhipeng<sup>1,2,4</sup>, Amos KIPKOECH<sup>1,3</sup>, WU Zengyuan<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHAO Ying<sup>1,4</sup>, Richard I. MILNE<sup>5</sup>, LI Zhipeng<sup>1,2,4</sup>, Amos KIPKOECH<sup>1,3</sup>, WU Zengyuan<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240901&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[<i>Boehmeria nivea</i> var. <i> strigosa</i>(Urticaceae), a new variety from Southwest China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240902&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Boehmeria nivea</i> var. <i>strigosa</i> Zeng Y. Wu &amp; Y. Zhao, a new variety of <i>B. nivea</i>(Urticaceae)from Southwest China, is here described based on evidence from morphology and molecular phylogeny. This new variety is mainly characterized by its green abaxial leaf blade, partly connate stipules, and densely patent strigose hairs on stems and potioles. The phylogenetic analysis based on <i>rbc</i>L, nrDNA and <i>rbc</i>L+nrDNA datasets, revealed that all individuals of <i>B. nivea</i> var. <i>strigosa</i> formed a monophyletic group. The conservation status of <i>B. nivea</i> var. <i>strigosa </i>is assessed as “Near Threatened”(NT)according to IUCN evaluation criteria. The discovery of this new variety is not only crucial for the taxonomy of ramie, but also provides reference for the exploration and utilization of ramie.]]></description>
<pubDate>2024/9/27 0:00:00</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHAO Ying<sup>1,4</sup>, Richard I. MILNE<sup>5</sup>, LI Zhipeng<sup>1,2,4</sup>, Amos KIPKOECH<sup>1,3</sup>, WU Zengyuan<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHAO Ying<sup>1,4</sup>, Richard I. MILNE<sup>5</sup>, LI Zhipeng<sup>1,2,4</sup>, Amos KIPKOECH<sup>1,3</sup>, WU Zengyuan<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240902&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[Three new records of lichen genus<i> Malmidea</i> from China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240903&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The purpose of this study is to investigate the species diversity of <i>Malmidea</i> in China and further identify its species composition and distribution. The lichen specimens collected from Yunnan Province were classified based on the investigation of lichen resources in the field and the collection of lichen specimens, and combined with the methods of morphology, anatomy and chemistry. Three new records of <i>Malmidea</i> were reported from China, <i>M. indica </i>(D. D. Awasthi &amp; M. R. Agarwal)Hafellner &amp; T. Sprib, <i>M. reunionis</i> Kalb and <i>M. hechicerae </i>Kalb. In this paper, detailed descriptions, morphology and anatomical pictures of the recorded species were provided, and comparison and discussion were made with similar species. A key to all known Chinese <i>Malmidea</i> species was also provided. This study enriches the diversity of <i>Malmidea</i> in China, and has some significance for conservation and study of lichen diversity of China.]]></description>
<pubDate>2024/9/27 0:00:00</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[WANG Lei<sup>1</sup>, WANG Xinyu<sup>2</sup>, XUE Junxia<sup>1</sup>, ZHANG Lulu<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Lei<sup>1</sup>, WANG Xinyu<sup>2</sup>, XUE Junxia<sup>1</sup>, ZHANG Lulu<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240903&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[Two newly recorded species of <i>Peltula</i> from China]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240904&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[To explore the species diversity of the genus <i>Peltula</i> Nyl. in Helan Mountain of Ningxia Hui Autonomous Region, the specimens of the genus <i>Peltula</i> Nyl. collected from Helan Mountain of Ningxia Hui Autonomous Region were classified by morph-anatomical, chemical and phylogenetic analysis of rDNA-ITS sequences. Two new records for China, <i>Peltula africana</i>(Jatta)Swinscow &amp; Krog and <i>P. impressa</i>(Vain.)Swinscow &amp; Krog, were identified. <i>P. africana</i> was mainly characterized by squamules undulate, 0.3-3.0 mm across, lower cortex cell palisade. <i>P. impressa</i> was mainly recognised by the black new type of soralia on top of the thallus, the hymenium I +, burgundy and about 64 ascospores. The morphological and anatomical characters of these two species were described in details, the differences with similar species were discussed, and the photos of morphological and anatomical structures of the two species were provided. The results enrich basic data for the genus <i>Peltula</i> Nyl. in China.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[WANG Siying<sup>1</sup>, ZHAO Gege<sup>1</sup>, LIANG Yongliang<sup>2</sup>, ZHU Yachao<sup>2</sup>, 
SUN Haoran<sup>2</sup>, TIAN Xinyao<sup>2</sup>, NIU Dongling<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Siying<sup>1</sup>, ZHAO Gege<sup>1</sup>, LIANG Yongliang<sup>2</sup>, ZHU Yachao<sup>2</sup>, 
SUN Haoran<sup>2</sup>, TIAN Xinyao<sup>2</sup>, NIU Dongling<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240904&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[A new combination and new synonym 
of <i>Anna</i> Pellegr.(Gesneriaceae)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240905&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Since the establishment of <i>Anna</i> Pellegr. in 1930, the taxonomic revisions of this genus have been infrequent. Early publications and revisions of <i>Anna</i> were based on specimens collected by foreign missionaries, which led to problems such as brief or inaccurate descriptions of traits and unclear species definition. When researching publication history, comparing morphology and investigating type locality of <i>Anna ophiorrhizoides</i>(Hemsl.)B. L. Burtt &amp; R. A. Davidson and <i>A. rubidiflora </i>S. Z. He, F. Wen &amp; Y. G. Wei, it was found that <i>Didymocarpus cavaleriei</i> H. L&#233;v. published by H. L&#233;veill&#233; in 1911 and <i>Anna rubidiflora</i> was actually the same species, and <i>Didymocarpus cavaleriei </i>was treated as a synonym of <i>Anna ophiorrhizoides. </i>After comparing the morphological characteristics of multiple populations of <i>A. ophiorrhizoides </i>and <i>A. rubidiflora</i>, it was found that the difference in their morphological characteristics lay in the corolla. It was not appropriate to use differences in corolla color as boundaries for the classificatory units of species. Taking into account the morphological characteristics and geographical distribution characteristics, it was proposed to treat <i>A. rubidiflora</i> as a variety of <i>A. ophiorrhizoides</i>. According to the regulations and suggestions in the 2018 <i>International Code of Nomenclature for Algae, Fungi, and Plants(Shenzhen Code</i>), a new combination and a name at new rank —— <i>A. ophiorrhizoides</i>(Hemsl.)B. L. Burtt &amp; R. A. Davidson var. <i>cavaleriei</i>(H. L&#233;v.)X. X. Bai &amp; F. Wen were proposed, and <i>A. rubidiflora</i> was treated as a synonym of the new combination.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[XIONG Xiaokai<sup>1</sup>, GU Jiangmiao<sup>1</sup>, WEN Fang<sup>2,3</sup>, BAI Xinxiang<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XIONG Xiaokai<sup>1</sup>, GU Jiangmiao<sup>1</sup>, WEN Fang<sup>2,3</sup>, BAI Xinxiang<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240905&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[Identification and expression analysis of bHLH transcription 
factors family in <i>Rhododendron delavayi</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240906&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Water deficiency is a critical factor that restricts the utilization of <i>Rhododendron delavayi</i> in landscaping. bHLH transcription factors are pivotal regulators of plant growth, development, and stress responses. This study aimed to identify members of the <i>R. delavayi</i> bHLH transcription factor(RdbHLH)family by utilizing the <i>R. delavayi</i> genome file and transcriptome data. Through bioinformatics methods, we analyzed various aspects, including gene structure, conserved motifs, phylogenetic relationships, protein physicochemical properties, <i>cis</i>-acting elements, protein interaction networks, and expression patterns. The results were as follows:(1)A total of 116 <i>RdbHLH</i> genes were identified, exhibiting significant variations in terms of amino acid composition and molecular weight of proteins. These genes were primarily weakly acidic hydrophilic proteins that function predominantly within the cell nucleus.(2)The <i>RdbHLH</i> family was categorized into 17 subfamilies, where motif structures were conserved within each subfamily but displayed noticeable differences between different subfamilies. Most RdbHLH proteins contained both Motif 1 and Motif 2 at the same time. The promoter region of these genes contained a substantial number of <i>cis</i>-acting elements associated with plant growth and development, hormone response, light response, and stress response.(3)<i>R. delavayi</i> responds to drought stress by activating signal transduction pathways and regulating osmotic pressure and flavonoid biosynthesis systems, leading to stress damage mitigation. Drought stress exerted an impact on the expression of 36 <i>RdbHLH</i> genes, with 12 genes displaying robust induction. Notably, <i>RdbHLH</i>49 and <i>RdbHLH</i>95 might play pivotal regulatory roles in enhancing plant resistance to drought stress. These research findings provide a theoretical basis for further investigations into the biological functions of <i>RdbHLH</i> genes and establish target gene resources for the breeding of superior horticultural varieties of <i>R. delavayi</i>.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[WANG Hongfei<sup>1</sup>, OU Jing<sup>1*</sup>, WANG Xiaojing<sup>2</sup>, KE Ke<sup>3</sup>, FAN Yu<sup>1</sup>, 
ZHOU Yumei<sup>1</sup>, FAN Xinyue<sup>1</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Hongfei<sup>1</sup>, OU Jing<sup>1*</sup>, WANG Xiaojing<sup>2</sup>, KE Ke<sup>3</sup>, FAN Yu<sup>1</sup>, 
ZHOU Yumei<sup>1</sup>, FAN Xinyue<sup>1</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240906&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[Identification and analysis of bHLH transcription factor 
family in red raspberry based on transcriptome sequencing]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240907&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[bHLH transcription factors are a large family of transcription factors in plants, which play important roles in plant growth and development, secondary metabolism regulation, and hormone response. Red raspberry fruit is rich in raspberry ketone. To investigate the role of bHLH transcription factor in the growth and development of red raspberry and the synthesis of raspberry ketone, members of the red raspberry bHLH gene family were identified and bioinformatics analysis of these genes were performed based on transcriptome sequencing of two red raspberry fruits, ‘Polka' and ‘Orange Legend'. The results were as follows:(1)A total of 95 bHLH transcription factor family members were identified in red raspberry fruits.(2)Most of the bHLH transcription factor family members were unstable hydrophobic proteins; and more than half of them were localized in the nucleus.(3)bHLH transcription factor N-terminal contained the conserved His5-Glu9-Arg13 sequence and C-terminal contained the conserved Leu sequence.(4)The phylogenetic tree divided the family members into 20 subfamilies, of which the R subfamily had the most members with 12.(5)The expression pattern map indicated that the bHLH transcription factor was expressed at a higher level during the green fruit stage and at a lower level during the ripening stage. The results provide a basis for screening bHLH transcription factors that are consistent with changes in raspberry ketone content and provide a reference for further exploring the function of red raspberry bHLH family.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[HE Zhimin<sup>1,2</sup>, ZHANG Junxin<sup>1,2</sup>, YU Liping<sup>1,2</sup>, HU Kang<sup>1,2</sup>, JI Fengqi<sup>1,2</sup>, 
HUANG Tiran<sup>1,2</sup>, YANG Mingfeng<sup>1,2*</sup>, MA Lanqing<sup>1,2</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HE Zhimin<sup>1,2</sup>, ZHANG Junxin<sup>1,2</sup>, YU Liping<sup>1,2</sup>, HU Kang<sup>1,2</sup>, JI Fengqi<sup>1,2</sup>, 
HUANG Tiran<sup>1,2</sup>, YANG Mingfeng<sup>1,2*</sup>, MA Lanqing<sup>1,2</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240907&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[Genome-wide identification and expression analysis 
of E3 ubiquitin-protein ligase U-box family 
in <i>Physcomitrium patens</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240908&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The U-box family encodes E3 ubiquitin ligase, which can specifically recognize the substrate and thus regulate the process of protein modification and degradation. In order to identificate the members of the <i>Physcomitrium patens </i>U-box family and to analyze their gene expression regularities, their physicochemical characteristics, evolutionary relationship, <i>cis</i>-acting element, tissue expression patterns and stress response were analyzed based on the whole sequencing data of <i>P. patens </i> through bioinformatics technology. The results were as follows:(1)A total of 31 U-box family members were identified in the whole genome of <i>P. patens</i> and were unevenly distributed on 14 chromosomes; their molecular weight sizes ranged from 37.75-117.49 kDa, and their isoelectric points ranged from 5.32-8.55.(2)The evolutionary tree showed that the U-box family members of <i>P. patens</i> were distributed in subfamilies I-IX, among which subfamily Ⅶ contained the largest number of members, with a total of 11 members accounting for about 36.67%. This indicated that <i>P. patens</i> was highly conserved and functionally diversified in the historical evolutionary process.(3)Promoter analysis yielded that <i>P. patens </i>U-box family members had elements that binded several hormones including GA and ABA.(4)Tissue expression analysis yielded that <i>P. patens</i> U-box family members was abundantly expressed mainly in the chloroplast, axoplast, and sporophyte S3 periods.(5)After simulated drought treatment with ABA, mannitol and saturated LiCl, it was found that the proposed stems of gametophytes were yellowed and the expression of<i> PpPUB</i>21 was significantly induced. It is hypothesized that the <i>P. patens</i> U-box family members plays an important role in growth and development and in response to adversity stress, and these findings provide a reference for further research on the U-box gene of <i>P. patens</i>.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[WU Xiaoai<sup>1</sup>, JIANG Shan<sup>1</sup>, CHEN Bo<sup>2</sup>, YAN Huiqing<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WU Xiaoai<sup>1</sup>, JIANG Shan<sup>1</sup>, CHEN Bo<sup>2</sup>, YAN Huiqing<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240908&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[Characteristics of leaf venation of <i>Mussaenda </i>
and its relative genera]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240909&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The classification of <i>Mussaenda</i> L. has been controversial due to the complex interspecific variation and hybridization within the genus. In order to explore the taxonomical significance of leaf venation characteristics between <i>Mussaenda</i> and its relative genera(<i>Schizomussaenda </i>Li and <i>Psudomussaenda </i>Wernham), and to provide data for the identification, development and utilization when they were regarded as the medical and garden plant resources, the leaf venation characteristics of 22 species of this group were observed by using the cleaning method. The cluster analysis was carried out based on the characteristics of leaf venation, and a classification key of the species was compiled. The results were as follows:(1)The characteristics of the leaf venation of <i>Mussaenda</i> and its relative genera had consistency, which were mainly reflected on that the primary veins were all pinnate, the frequency of inter-secondary veins was less than one per areolation, the angles between the major secondary veins and the midveins were acute, the tertiary veins were mostly penetrating, and the arrangement of the areolation were all irregular.(2)The characteristics of the leaf venation with taxonomic value among genera or species within genera included the type of major secondary vein venation type, the angle between major secondary vein and midvein, the major secondary vein spacing, the connection between major secondary vein and midvein, the existence of inter-secondary vein and intramarginal secondary vein, the penetration type of intercostal tertiary vein, the type of quaternary vein, the branching of freely ending veinlet, and the areole development.(3)According to the cluster analysis, 22 species of this group were clustered into 12 branches, and <i>Schizomussaenda </i>and <i>Psudomussaenda</i> were not clustered into one branch respectively, showing a relatively close genetic relationship. In conclusion, the leaf venation characteristics of <i>Mussaenda</i> and its related taxa can provide new information for the classification of the plants.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHANG Duo<sup>1</sup>, LI Jin<sup>2</sup>, DUAN Tingting<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Duo<sup>1</sup>, LI Jin<sup>2</sup>, DUAN Tingting<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240909&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[Characterization of genetic difference and phylogenetic 
relationship between <i>Schizocapsa guangxiensis</i> and 
<i>Tacca plantaginea</i> based on chloroplast genome]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240910&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The taxonomy of <i>Tacca</i> remains is controversial all the time. <i>Schizocapsa guangxiensis</i> is considered to be the same species as <i>Tacca plantanginea</i>, but some taxonomists classify them into different species based on their morphological differences. In order to clarify the genetic differences and phylogenetic relationship between <i>Schizocapsa guangxiensis</i> and <i>Tacca plantanginea</i>, this study conducted high-throughput DNA sequencing of <i>Schizocapsa guangxiensis</i>, assembled a complete chloroplast genome using bioinformatics software, and compared it with the published <i>Tacca plantanginea</i> chloroplast genome. The results were as follows:(1)The chloroplast genome size of <i>Schizocapsa guangxiensis</i> and <i>Tacca plantanginea</i> was 162 149 bp and 160 749 bp, respectively, and they had the same GC content(36.90%). Notably, the gene types and gene amount were exactly the same in these two species, including 89 protein-coding genes and 37 tRNA genes, and 6 rRNA genes.(2)Codon preference analysis showed that there were certain differences in the codon frequencies used by the two species, but they both prefered codons ending in A/T(U).(3)Compared with <i>T. plantanginea</i>, the SSC boundary of <i>Schizocapsa guangxiensis</i> had obvious expansion, which was the main factor leading to the length variant in chloroplast genome between the two species.(4)There were some sequence divergences between <i>S. guangxiensis</i> and <i>Tacca plantanginea</i> in the LSC and SSC regions, especially the intergenic region, which can be exploited as species-specific molecular marker.(5)Phylogenetic results showed that <i>Schizocapsa guangxiensis</i> and <i>Tacca plantanginea</i> had a rather distant genetic relationship. Although <i>Schizocapsa guangxiensis</i> was placed in <i>Tacca</i>, they belong to two different species. This study enriches the genetic information of the chloroplast genome of <i>S. guangxiensis</i> and provides a theoretical basis for species classification, genetic diversity analysis and species protection of <i>S. guangxiensis</i>.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[MA Yunying<sup>1</sup>, DENG Yongbiao<sup>1</sup>, LV Huqian<sup>1,2</sup>, ZHOU Qianru<sup>1</sup>, 
LI Jingjian<sup>1</sup>, LU Zhaocen<sup>3*</sup>, XIE Wenjuan<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>MA Yunying<sup>1</sup>, DENG Yongbiao<sup>1</sup>, LV Huqian<sup>1,2</sup>, ZHOU Qianru<sup>1</sup>, 
LI Jingjian<sup>1</sup>, LU Zhaocen<sup>3*</sup>, XIE Wenjuan<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240910&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[Plastid capture history of subsect. <i>Campylolepides</i> 
and section <i>Ilex</i>(Fagaceae:<i> Quercus</i>)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240911&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Quercus</i> subsect. <i>Campylolepides</i> contains three species: <i>Q. acutissima</i>, <i>Q. variabilis</i> and <i>Q. chenii</i>, which is the East Asian clade of <i>Quercus</i> section <i>Cerris</i>. Species formation and phylogeography of whole subsection or species within the subsection have been studied in detail. It has been also found that section <i>Cerris</i> had an ancient gene introgression with section <i>Ilex</i>, which led to the plastid capture. However, the specific evolutionary history of plastids in subsect. <i>Campylolepides</i> and section <i>Ilex </i>remains unclear. Our study performed low-coverage whole genome sequencing on 15 samples from section<i> Ilex</i> and integrated previously published data from subsect. <i>Campylolepides</i> and its relatives, resulting in a total of 325 resequencing data, of which 276 individuals were from three subsect. <i>Campylolepides</i> species and 19 populations. We assembled 325 plastids to perform phylogeographic analysis. The results were as follows:(1)There were shared haplotypes among three species of subsect. <i>Campylolepides</i>, but the plastid haplotypes of the entire subsect. <i>Campylolepides</i> form a monophyletic branch nested within section <i>Ilex</i> species which are distributed from central China to Liangshan, Sichuan.(2)A relictual haplotype of subsect. <i>Campylolepides</i> from the Liaodong Peninsula clustered with <i>Q. pseudosetulosa</i>, a specie of the section <i>Ilex</i>.(3)Both plastid capture events occurred in the middle Miocene, after which no plastid capture occurred between subsect. <i>Campylolepides</i> and section <i>Ilex</i>. It is hypothesized that subsect. <i>Campylolepides</i> and section <i>Ilex</i> have formed almost complete reproductive isolation. The study demonstrates that section <i>Ilex</i> and subsect. <i>Campylolepides</i> have undergone ancient plastid capture events in their evolution history, ultimately lead to the gradual formation of relatively independent evolutionary paths.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[YU Shuliang<sup>1</sup>, LI Zhimin<sup>1</sup>, MA Xiangguang<sup>2*</sup>, SUN Wenguang<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YU Shuliang<sup>1</sup>, LI Zhimin<sup>1</sup>, MA Xiangguang<sup>2*</sup>, SUN Wenguang<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240911&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[Chloroplast genome features and phylogenetic 
analysis of <i>Artemisia parviflora</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240912&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[To explore the structural features of <i>Artemisia parviflora</i> chloroplast genome and its systematic position, high-throughput sequencing technology were employed for genome sequencing and bioinformatics tools for analyzing. The results were as follows:(1)The chloroplast genome of <i>A. parviflora</i> was 151 047 bp, with a typical circular double-stranded tetrad structure, and the GC content was 37.5%.(2)Total 115 unique genes were annotated, including 81 protein-coding genes, 4 rRNA genes, and 30 tRNA genes.(3)Sixty-eight simple sequence repeats(SSRs)and 37 long repeat sequences were detected.(4)The codon usage bias was weak in the <i>A. parviflora</i> chloroplast genome, and natural selection mainly contributed to the codon usage bias. High-frequency codons tend to ended with A/U.(5)There was no obvious expansion or contraction of the inverted repeat(IR)regions. Five high variation regions(<i>trnH-psbA</i>, <i>rpl</i>16<i>-rps</i>3, <i>ycf</i>15<i>-trnL-UAG</i>, <i>ndhA</i>, and <i>ycf</i>1)were identified which could be used as potential molecular markers for identifying subgen. <i>Dracunculus </i>species.(6)Phylogenetic analysis revealed the systematic position of <i>A. parviflora</i> within subgen. <i>Dracunculus</i> and elucidated the phylogenetic relationships among the various subgenera of <i>Artemisia</i>. This study provides the reference for future molecular marker development and phylogenetic research of <i>Artemisia</i> species.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[LI Zhifang, CHEN Liling, LUO Shujie, LIU Tianmeng<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Zhifang, CHEN Liling, LUO Shujie, LIU Tianmeng<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240912&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[Floral characteristics and butterfly wing 
pollination of <i>Lycoris aurea</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240913&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Lycoris aurea</i> is a perennial herbaceous plant with important medicinal and ornamental values in the genus <i>Lycoris</i> Herb, the family Amaryllidaceae. The flower has a spider shape with highly exserted stigmas and anthers, which may represent a unique pollination type. In order to explore this type of pollination, we studied its floral characteristics, breeding system, and floral visitors and their behaviors. The results were as follows:(1)The single flower lasted(5.9&#177;0.1)d and the pollen-ovule ratio(P/O)reached about 23 000. The flowers showed reverse herkogamy. On the beginning of flowering, the style and filaments were separated and the angle between them was about 30°. The style gradually moved towards the filaments in the middle and later stages and were finally on the same line with the stigma 2-3 cm higher than the anthers. The stigmas were receptive throughout the flowering period.(2)The breeding system test was self-compatible and bagged flowers cannot set fruit, indicating that pollinators were necessary for pollen transfer. Supplemental hand pollination significantly increased fruit production, indicating the existence of pollen limitation.(3)Four species of swallowtail butterfly were the effective pollinators. Due to the existence of herkogamy in <i>L. aurea</i>, on the beginning of flowering, their hindwings were likely to come into contact with the flattened anthers. Their hindwings might touch the stigma in the middle and later stages and thus the process of pollen transfer was accomplished. In conclusion, this study shows that the uqique floral characteristics of <i>L. aurea</i> are adapted for butterfly wing pollination and also will lay the foundation for its conservation and sustainable utilization.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[LIAO Rui, LING Xinyu, WU Yuanhui, ZHU Xingfu<sup>*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIAO Rui, LING Xinyu, WU Yuanhui, ZHU Xingfu<sup>*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240913&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[Comparative analysis of chloroplast genomes and phylogenetic analysis of <i>Vitex</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240914&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Vitex</i> L. is widely distributed in tropical and subtropical areas, mostly as woody trees or shrubs, and contains many plants with medicinal, ornamental and ecological values. To understand the characteristics of <i>Vitex</i> chloroplast genomes, the phylogenetic position and interspecific relationships of the genus, the chloroplast genome sequence of <i>V. agnus-castus</i> was firstly obtained by <i>de novo</i> assembly and annotation, the genome structure, codon preference, high variation region and repeat sequence were then analyzed with 11 published chloroplast genome sequences of <i>Vitex</i>, and then phylogenetic analysis was conducted. The results were as follows:(1)The chloroplast genome of <i>V. agnus-castus</i> was a typically quadripartite structure with a total length of 154 444 bp, in which the length of the large single copy(LSC)region, the small single copy(SSC)region and the inverted repeat(IR)region were 85 229, 17 915 and 51 400 bp, respectively. The chloroplast genome encoded 132 genes, including 87 protein-coding genes, 37 tRNA genes and 8 rRNA genes.(2)The 12 chloroplast genomes of <i>Vitex</i> were highly conserved in terms of genome length, boundary position of IR region, number of encoded genes and GC content.(3)A total of 31 high frequency codons and six common optimal codons were detected in 12 chloroplast genomes of <i>Vitex</i>. Further, the results of ENC-plot, PR2-plot and neutral plot analysis indicated that codon preference was mainly influenced by natural selection.(4)In addition, a total of 14 highly variable regions and 519 simple sequence repeats(SSRs)were detected in the 12 chloroplast genomes of <i>Vitex</i>.(5)The molecular phylogenetic inference in this study supported that <i>Vitex</i> belonged to the subfamily Viticoideae(Lamiaceae), not Verbenaceae. Moreover, phylogenetic inference also provided some understanding of the controversial relationships among <i>V. trifolia</i>, <i>V. bicolo</i>r and <i>V. rotundifolia</i>, suggesting that <i>V. rotundifolia</i> was considered as a separate species. This study not only enriches the information of genetic resources of <i>V. agnus-castus</i>, increases the understanding of the chloroplast genomes of <i>Vitex</i>, provides candidate molecular markers for population genetics studies of <i>Vitex</i>, but also proves the effectiveness of chloroplast genome sequence in the phylogenetic reconstruction of <i>Vitex</i>.]]></description>
<pubDate>2024/9/27 0:00:00</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[XIU Zhiying<sup>1</sup>, ZHAO Yanling<sup>1</sup>, CHENG Yongqin<sup>2</sup>, JIA Yun<sup>3</sup>, YANG Yanci<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XIU Zhiying<sup>1</sup>, ZHAO Yanling<sup>1</sup>, CHENG Yongqin<sup>2</sup>, JIA Yun<sup>3</sup>, YANG Yanci<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240914&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[Comparative analysis of chloroplast genomes 
and phylogenetic analysis of <i>Vitex</i>]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240915&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Vitex</i> L. is widely distributed in tropical and subtropical areas, mostly as woody trees or shrubs, and contains many plants with medicinal, ornamental and ecological values. To understand the characteristics of <i>Vitex</i> chloroplast genomes, the phylogenetic position and interspecific relationships of the genus, the chloroplast genome sequence of <i>V. agnus-castus</i> was firstly obtained by <i>de novo</i> assembly and annotation, the genome structure, codon preference, high variation region and repeat sequence were then analyzed with 11 published chloroplast genome sequences of <i>Vitex</i>, and then phylogenetic analysis was conducted. The results were as follows:(1)The chloroplast genome of <i>V. agnus-castus</i> was a typically quadripartite structure with a total length of 154 444 bp, in which the length of the large single copy(LSC)region, the small single copy(SSC)region and the inverted repeat(IR)region were 85 229, 17 915 and 51 400 bp, respectively. The chloroplast genome encoded 132 genes, including 87 protein-coding genes, 37 tRNA genes and 8 rRNA genes.(2)The 12 chloroplast genomes of <i>Vitex</i> were highly conserved in terms of genome length, boundary position of IR region, number of encoded genes and GC content.(3)A total of 31 high frequency codons and six common optimal codons were detected in 12 chloroplast genomes of <i>Vitex</i>. Further, the results of ENC-plot, PR2-plot and neutral plot analysis indicated that codon preference was mainly influenced by natural selection.(4)In addition, a total of 14 highly variable regions and 519 simple sequence repeats(SSRs)were detected in the 12 chloroplast genomes of <i>Vitex</i>.(5)The molecular phylogenetic inference in this study supported that <i>Vitex</i> belonged to the subfamily Viticoideae(Lamiaceae), not Verbenaceae. Moreover, phylogenetic inference also provided some understanding of the controversial relationships among <i>V. trifolia</i>, <i>V. bicolo</i>r and <i>V. rotundifolia</i>, suggesting that <i>V. rotundifolia</i> was considered as a separate species. This study not only enriches the information of genetic resources of <i>V. agnus-castus</i>, increases the understanding of the chloroplast genomes of <i>Vitex</i>, provides candidate molecular markers for population genetics studies of <i>Vitex</i>, but also proves the effectiveness of chloroplast genome sequence in the phylogenetic reconstruction of <i>Vitex</i>.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[XIU Zhiying<sup>1</sup>, ZHAO Yanling<sup>1</sup>, CHENG Yongqin<sup>2</sup>, JIA Yun<sup>3</sup>, YANG Yanci<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XIU Zhiying<sup>1</sup>, ZHAO Yanling<sup>1</sup>, CHENG Yongqin<sup>2</sup>, JIA Yun<sup>3</sup>, YANG Yanci<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240915&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[Response of <i>Carex moorcroftii</i> leaf 
anatomical structure to habitat aridification]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240916&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Leaves are the largest and more sensitive vegetative organs exposed to external environmental conditions. In order to investigate the effects of habitat aridification on the leaf anatomical structure of wetland plants, <i>Carex moorcroftii</i> leaf plots were set up along the gradient of habitat aridification, and the response of leaf anatomical structure to habitat aridification was analyzed in this study. The results were as follows:(1)The epidermal cells, bulliform cells and air cavity area on the abaxial surface of leaf tip and leaf base, leaf thickness and mechanical tissue thickness at leaf base were significantly positively correlated with soil volumetric moisture content(<i>R</i><sup>2</sup>=0.06-0.34, <i>P</i>&lt;0.01); the paraxial cuticle thickness, cell area, number of vascular bundles in parts of leaf tip, leaf middle and leaf base, and diameter of vascular bundle in leaf middle were significantly negatively correlated with soil volumetric moisture content(<i>R</i><sup>2</sup>=0.08-0.53, <i>P</i>&lt;0.01).(2)The anatomical structure of <i>C. moorcroftii</i> leaf had great plasticity(0.53-0.94)and variability(18%-63%), and bulliform cells, air cavities, and paraxial epidermal cells had the greatest plasticity and variability, and the plasticity index and the coefficient of variation of leaf base anatomical structure were significantly higher than that of leaf tip and leaf middle(<i>P</i>&lt;0.05). When the habitat was aridified, <i>C. moorcroftii</i> leaf adapt to the arid habitat by thickening the cuticle on the paraxial surface, increasing the epidermal cell area, decreasing the air cavity area, and differentiating middle cells, and mainly adopted protective and frugal strategies to adapt to the arid habitat. The results of this study are helpful to reveal the response strategies of <i>C. moorcroftii </i>leaf anatomical structure to arid habitat, and provide theoretical reference for protection and vegetation restoration of alpine meadow.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[CAI Huiwen<sup>1</sup>, WANG Hongbin<sup>2</sup>, ZHANG Dacai<sup>1*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CAI Huiwen<sup>1</sup>, WANG Hongbin<sup>2</sup>, ZHANG Dacai<sup>1*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240916&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[Photosynthetic characteristics of <i>Yulania denudata</i> 
with variegated leaf based on anatomy]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240917&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[To reveal the causes of photosynthetic characteristics of <i>Yulania denudata</i> with variegated leaf, the green leaves, variegated leaves and yellow leaves of <i>Y. denudata</i> with variegated leaf were used as experimental materials. The anatomical structure and photosynthetic characteristics in three types of leaves were compared from the aspects of photosynthetic pigment content, leaf anatomical structure and light response curve. The results were as follows:(1)The yellow leaf spots of <i>Y. denudata</i> with variegated leaf were chlorophyll-type leaf spots formed by the decrease of chlorophyll content due to the abnormal structure of chloroplasts.(2)The structure of thylakoids in the yellow region of <i>Y. denudata</i> with variegated leaf was abnormal, and ATP synthesis was blocked, which hindered the progress of photosynthesis.(3)The anatomical structure showed that the palisade tissue of the green leaf was developed, the chloroplast integrity and pigment content were higher than those of the variegated leaf and the yellow leaf, and the net photosynthetic rate was higher.(4)There were significant differences in the maximum net photosynthetic rate and light saturation point between the green leaf and the variegated leaf, and the green leaf could withstand a wider range of bright light than the variegated leaf. This study further elucidates that the chloroplast structure of <i>Y. denudata</i> with variegated leaf affects its photosynthetic characteristics, and provides a reference for the breeding of excellent germplasm of <i>Y. denudata</i> with variegated leaf.]]></description>
<pubDate>2024/9/27 10:20:58</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[ZHU Kaili<sup>1,2</sup>, YE Kang<sup>2</sup>, SONG Xiqiang<sup>1</sup>, QIN Jun<sup>2</sup>, SHAO Wen<sup>2</sup>, HU Yonghong<sup>1,2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHU Kaili<sup>1,2</sup>, YE Kang<sup>2</sup>, SONG Xiqiang<sup>1</sup>, QIN Jun<sup>2</sup>, SHAO Wen<sup>2</sup>, HU Yonghong<sup>1,2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240917&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[Pollen morphology and leaf epidermal micromorphology 
of 10 species of sect. <i>Tuberculata</i>(<i>Camellia</i> L.)]]></title>
<link><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240918&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[To provide research data for the phylogenetic evolution, classification and identification of plants in sect. <i>Tuberculata</i> of <i>Camellia </i>genus, 10 species of the section, leaf epidermal micromorphology and pollen morphology were observed by light microscope and scanning electron microscopy(SEM)and based on pollen features and leaf epidermal features to clustered separately. The results were as follows:(1)10 species had no significant difference in pollen morphology and size, the pollen shape was subspheroidal, prolate or oblatesphere; the outline in polar view was trilete rounded or trilete regular teiangular; the outline in equatorial view was oblong or fusiform, P/E ranged from 0.85 to 1.16; the aperature type was tricolporate aperature. The exine sculpture was significantly different, the feature had coarsely warty, foveolate reticulate or rugulate with beadedmun, and had important classification value for sect. <i>Tuberculata</i>.(2)The cluster analysis of the measurement index showed that when the Euclidean distance was 4.5, the 10 species were divided into four groups, and some of the classification results were the same as the macroscopic morphological classification.(3)The leaf epidermal cells of 10 species were irregular or polygon, with great morphological differences among species. There were glands in the upper and lower epidermis of <i>C. zengii</i>, <i>C. rhytidophylla</i> and <i>C. rubimuricata</i>; cyclic type stomatal apparatuses were only distributed in the lower epidermis; anticlinal wall pattern were sinuolate, sinuous, repand and sinuate.(4)The cell size and stomatal features(size and density)of leaf epidermis micromorphology were significantly different between species. This study shows that pollen morphology and leaf epidermal micromorphology are diverse in sect. <i>Tuberculata</i>, which can be used as the basis for distinguishing some closely related species in sect. <i>Tuberculata.]]></description>
<pubDate>2024/9/27 10:20:59</pubDate>
<category><![CDATA[Special Issue：Plant Classification and System Evolution]]></category>
<author><![CDATA[YAN Chao<sup>1</sup>, XIAO Xu<sup>1</sup>, RAN Zhaohui<sup>1</sup>, LI Zhi<sup>1,2*</sup>]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YAN Chao<sup>1</sup>, XIAO Xu<sup>1</sup>, RAN Zhaohui<sup>1</sup>, LI Zhi<sup>1,2*</sup></atom:name>
</atom:author>
<guid><![CDATA[http://gxzw.ijournals.cn/gxzwen/ch/reader/view_abstract.aspx?file_no=20240918&flag=1]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
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