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Figure 3. Ninety-five per cent maximum parsimony networks obtained for the 12 in Mitochondrial DNA genetic variation and phylogeography of the recently described vole species Proedromys liangshanensis Liu, Sun, Zeng and Zhao, 2007 (Rodentia: Arvicolinae)
No full textFigure 3. Ninety-five per cent maximum parsimony networks obtained for the 12 haplotypes in Proedromys liangshanensis. Circle sizes are proportional to haplotype frequencies.Published as part of Chen, Weicai, Hao, Haibang, Liu, Yang, Chen, Shunde, Zhang, Xiuyue, Liu, Shaoying & Yue, Bisong, 2010, Mitochondrial DNA genetic variation and phylogeography of the recently described vole species Proedromys liangshanensis Liu, Sun, Zeng and Zhao, 2007 (Rodentia: Arvicolinae), pp. 2693-2703 in Journal of Natural History 44 (43-44) on page 2699, DOI: 10.1080/00222933.2010.501911, http://zenodo.org/record/521200
A new species of Tamiops (Rodentia, Sciuridae) from Sichuan, China
No full textLiu, Shaoying, Tang, Mingkun, Murphy, Robert W., Liu, Yinxun, Wang, Xuming, Wan, Tao, Liao, Rui, Tang, Keyi, Qing, Jiao, Chen, Shunde, Li, Song (2022): A new species of Tamiops (Rodentia, Sciuridae) from Sichuan, China. Zootaxa 5116 (3): 301-333, DOI: 10.11646/zootaxa.5116.3.
FIGURE 3 in Molecular phylogenetics and diversity of the Himalayan shrew (Soriculus nigrescens Gray, 1842) (Eulipotyphla, Soricidae) in Southwest China
No full textFIGURE 3: A: Plot showing JK values for different K values tested. The K with the highest JK value is most likely to represent the true number of clusters; B: The linear relationship between LnP(D) and the number of clusters. C: Bayesian clustering results at K = 3 from the structure analysis.Published as part of Jiang, Haijun, Fu, Changkun, Tang, Keyi, Li, Fengjun, Faiz, Abu Ul Hassan, Guo, Keji, Liu, Shaoying & Chen, Shunde, 2023, Molecular phylogenetics and diversity of the Himalayan shrew (Soriculus nigrescens Gray, 1842) (Eulipotyphla, Soricidae) in Southwest China, pp. 61-78 in Zootaxa 5263 (1) on page 66, DOI: 10.11646/zootaxa.5263.1.3, http://zenodo.org/record/779780
Mitochondrial DNA genetic variation and phylogeography of the recently described vole species<i>Proedromys liangshanensis</i>Liu, Sun, Zeng and Zhao, 2007 (Rodentia: Arvicolinae)
No full textFigure 4. Expected (solid line) and observed (broken lines) mismatch distribution of Proedromys liangshanensis.Published as part of Chen, Weicai, Hao, Haibang, Liu, Yang, Chen, Shunde, Zhang, Xiuyue, Liu, Shaoying & Yue, Bisong, 2010, Mitochondrial DNA genetic variation and phylogeography of the recently described vole species Proedromys liangshanensis Liu, Sun, Zeng and Zhao, 2007 (Rodentia: Arvicolinae), pp. 2693-2703 in Journal of Natural History 44 (43-44) on page 2700, DOI: 10.1080/00222933.2010.501911, http://zenodo.org/record/521200
FIGURE 2 in A new species of Tamiops (Rodentia, Sciuridae) from Sichuan, China
No full textFIGURE 2. Bayesian inference (BI) phylogenetic trees derived from CYTB and three concatenated nuDNA genes. Numbers above branches refer to Bayesian posterior probabilities. Outgroups included species of the genera Callosciurus, Sundasciurus, and Dremomys.Published as part of Liu, Shaoying, Tang, Mingkun, Murphy, Robert W., Liu, Yinxun, Wang, Xuming, Wan, Tao, Liao, Rui, Tang, Keyi, Qing, Jiao, Chen, Shunde & Li, Song, 2022, A new species of Tamiops (Rodentia, Sciuridae) from Sichuan, China, pp. 301-333 in Zootaxa 5116 (3) on page 306, DOI: 10.11646/zootaxa.5116.3.1, http://zenodo.org/record/637214
FIGURE 2 in Molecular phylogenetics and diversity of the Himalayan shrew (Soriculus nigrescens Gray, 1842) (Eulipotyphla, Soricidae) in Southwest China
No full textFIGURE 2: Maximum Likelihood and Bayesian phylogenetic trees based on the mitochondrial Cyt-B (A) and nuclear (APOB, BRCA-1, and RAG-2) (B) sequences. Branch numbers refer to BEAST posterior probabilities (Left: PP), ML posterior probabilities (Middle: PP), and ML bootstrap support values (Right: BS). The mtDNA and nuDNA lineages have been labeled with different colors: blue for Clade A, red for Clade B, and purple for Clade YN. The abbreviations represent the sampling sites (DR: Dingri; NLM: Nielamu; YD: Yadong; MT-L: Motuo low altitude; MT-H: Motuo high altitude; BM: Bomi; BY: Bayi; ML: Milin; GBJD: Gongbujiangda; LX: Langxian).Published as part of Jiang, Haijun, Fu, Changkun, Tang, Keyi, Li, Fengjun, Faiz, Abu Ul Hassan, Guo, Keji, Liu, Shaoying & Chen, Shunde, 2023, Molecular phylogenetics and diversity of the Himalayan shrew (Soriculus nigrescens Gray, 1842) (Eulipotyphla, Soricidae) in Southwest China, pp. 61-78 in Zootaxa 5263 (1) on page 65, DOI: 10.11646/zootaxa.5263.1.3, http://zenodo.org/record/779780
FIGURE 2 in Molecular phylogeny of Asiatic Short-Tailed Shrews, genus Blarinella Thomas, 1911 (Mammalia: Soricomorpha: Soricidae) and its taxonomic implications
No full textFIGURE 2. Phylogeny of the genus Blarinella derived from maximum likelihood and Bayesian analyses of cyt-b and cyt-b + 16S rRNA + ApoB fragments. Node values above branches indicate ML bootstrap values and Bayesian posterior probabilities of cyt-b; node numbers under the branches indicate Bayesian posterior probabilities and ML bootstrap values of cyt-b +16S rRNA + ApoB.Published as part of Chen, Shunde, Liu, Shaoying, Liu, Yang, He, Kai, Chen, Weicai, Zhang, Xiuyue, Fan, Zhenxin, Tu, Feiyun, Jia, Xiaodong & Yue, Bisong, 2012, Molecular phylogeny of Asiatic Short-Tailed Shrews, genus Blarinella Thomas, 1911 (Mammalia: Soricomorpha: Soricidae) and its taxonomic implications, pp. 43-53 in Zootaxa 3250 (1) on page 48, DOI: 10.11646/zootaxa.3250.1.3, http://zenodo.org/record/524918
FIGURE 1 in Molecular phylogenetics and diversity of the Himalayan shrew (Soriculus nigrescens Gray, 1842) (Eulipotyphla, Soricidae) in Southwest China
No full textFIGURE 1: Map of Southwest China showing the sampling localities of S. nigrescens included in this study. Locality numbers are presented in Table 1, and the lineages have been labeled with different colors: blue for Clade A, red for Clade B, and purple for Clade YN. The sample of Nepal represents the collection site of the sequence downloaded from Genbank. Shaded area represents the distribution map of S. nigrescens from the Handbook Mammals of the World and Global Biodiversity Information Facility (GBIF: https://www.gbif.org/).Published as part of Jiang, Haijun, Fu, Changkun, Tang, Keyi, Li, Fengjun, Faiz, Abu Ul Hassan, Guo, Keji, Liu, Shaoying & Chen, Shunde, 2023, Molecular phylogenetics and diversity of the Himalayan shrew (Soriculus nigrescens Gray, 1842) (Eulipotyphla, Soricidae) in Southwest China, pp. 61-78 in Zootaxa 5263 (1) on page 64, DOI: 10.11646/zootaxa.5263.1.3, http://zenodo.org/record/779780
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
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