Translation: I don't like what the paper says so it must be wrong.
I could show you more papers but you'll just keep making excuses.
Here's another one (not written by those backwards science-illiterate Chinese.)
No, I told you exactly why I had issues with the paper in question. And yes, that journal is not well regarded, not even in China. And no, I never claimed Chinese were "backwards" or "science-illiterate." Maybe you are projecting your own short-comings? Freudian??
Since you like to cite papers you don't understand and never read, here are few more for you. Tell me why they are all wrong.
Nature Reviews Genetics 13, 303-314 (May 2012) | doi:10.1038/nrg3186
Molecular phylogenetics: principles and practice
Ziheng Yang & Bruce Rannala
Abstract
Phylogenies are important for addressing various biological questions such as relationships among species or genes, the origin and spread of viral infection and the demographic changes and migration patterns of species. The advancement of sequencing technologies has taken phylogenetic analysis to a new height. Phylogenies have permeated nearly every branch of biology, and the plethora of phylogenetic methods and software packages that are now available may seem daunting to an experimental biologist. Here, we review the major methods of phylogenetic analysis, including parsimony, distance, likelihood and Bayesian methods. We discuss their strengths and weaknesses and provide guidance for their use
http://www.nature.com/nrg/journal/v13/n5/full/nrg3186.html
The Impact of Molecular Data on Our Understanding of Bee Phylogeny and Evolution
Annual Review of Entomology
Vol. 58: 57-78 (Volume publication date January 2013)
First published online as a Review in Advance on August 28, 2012
DOI: 10.1146/annurev-ento-120811-153633
Bryan N. Danforth,1* Sophie Cardinal,2 Christophe Praz,3 Eduardo A.B. Almeida,4 and Denis Michez5
ABSTRACTOur understanding of bee phylogeny has improved over the past fifteen years as a result of new data, primarily nucleotide sequence data, and new methods, primarily model-based methods of phylogeny reconstruction. Phylogenetic studies based on single or, more commonly, multilocus data sets have helped resolve the placement of bees within the superfamily Apoidea; the relationships among the seven families of bees; and the relationships among bee subfamilies, tribes, genera, and species. In addition, molecular phylogenies have played an important role in inferring evolutionary patterns and processes in bees. Phylogenies have provided the comparative framework for understanding the evolution of host-plant associations and pollen specialization, the evolution of social behavior, and the evolution of parasitism. In this paper, we present an overview of significant discoveries in bee phylogeny based primarily on the application of molecular data. We review the phylogenetic hypotheses family-by-family and then describe how the new phylogenetic insights have altered our understanding of bee biology.
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RECENT ADVANCES IN THE (MOLECULAR) PHYLOGENY OF VERTEBRATES
Annual Review of Ecology, Evolution, and Systematics
Vol. 34: 311-338 (Volume publication date November 2003)
First published online as a Review in Advance on September 2, 2003
DOI: 10.1146/annurev.ecolsys.34.011802.132351
Axel Meyer
Rafael Zardoya
ABSTRACT▪ Abstract  The analysis of molecular phylogenetic data has advanced the knowledge of the relationships among the major groups of living vertebrates. Whereas the molecular hypotheses generally agree with traditional morphology-based systematics, they sometimes contradict them. We review the major controversies in vertebrate phylogenetics and the contribution of molecular phylogenetic data to their resolution: (a) the mono-paraphyly of cyclostomes, (b) the relationships among the major groups of ray-finned fish, (c) the identity of the living sistergroup of tetrapods, (d) the relationships among the living orders of amphibians, (e) the phylogeny of amniotes with particular emphasis on the position of turtles as diapsids, (f) ordinal relationships among birds, and (g) the radiation of mammals with specific attention to the phylogenetic relationships among the monotremes, marsupial, and placental mammals. We present a discussion of limitations of currently used molecular markers and phylogenetic methods as well as make recommendations for future approaches and sets of marker genes
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A Molecular Phylogeny of Phytophthora and Related Oomycetes
D.E.L. Cookea, 1, A. Drenthb, J.M. Duncana, G. Wagelsb, C.M. Brasier
Fungal Genetics and Biology
Volume 30, Issue 1, June 2000, Pages 1732
Abstract
Phylogenetic relationships among 50 Phytophthora species and between Phytophthora and other oomycetes were examined on the basis of the ITS sequences of genomic rDNA. Phytophthora grouped with Pythium, Peronospora, and Halophytophthora, distant from genera in the Saprolegniales. Albugo was intermediate between these two groups. Unlike Pythium, Phytophthora was essentially monophyletic, all but three species forming a cluster of eight clades. Two clades contained only species with nonpapillate sporangia. The other six clades included either papillate and semipapillate, or semipapillate and nonpapillate types, transcending traditional morphological groupings, which are evidently not natural assemblages. Peronospora was related to P. megakarya and P. palmivora and appears to be derived from a Phytophthora that has both lost the ability to produce zoospores and become an obligate biotroph. Three other Phytophthoras located some distance from the main PhytophthoraPeronospora cluster probably represent one or more additional genera.
A Molecular Phylogeny of Phytophthora and Related Oomycetes
Science 28 January 2005:
Vol. 307 no. 5709 pp. 580-584
DOI: 10.1126/science.1105113
Report
A Molecular Phylogeny for Bats Illuminates Biogeography and the Fossil Record
Emma C. Teeling1,2,*, Mark S. Springer3,*, Ole Madsen4, Paul Bates5, Stephen J. O'Brien6,*, William J. Murphy
AbstractBats make up more than 20% of extant mammals, yet their evolutionary history is largely unknown because of a limited fossil record and conflicting or incomplete phylogenies. Here, we present a highly resolved molecular phylogeny for all extant bat families. Our results support the hypothesis that megabats are nested among four major microbat lineages, which originated in the early Eocene [52 to 50 million years ago (Mya)], coincident with a significant global rise in temperature, increase in plant diversity and abundance, and the zenith of Tertiary insect diversity. Our data suggest that bats originated in Laurasia, possibly in North America, and that three of the major microbat lineages are Laurasian in origin, whereas the fourth is Gondwanan. Combining principles of ghost lineage analysis with molecular divergence dates, we estimate that the bat fossil record underestimates (unrepresented basal branch length, UBBL) first occurrences by, on average, 73% and that the sum of missing fossil history is 61%.
A Molecular Phylogeny for Bats Illuminates Biogeography and the Fossil Record
Molecular phylogeny and divergence times of drosophilid species.
C A Russo, N Takezaki and M Nei
Mol Biol Evol (1995) 12 (3): 391-404
Abstract
The phylogenetic relationships and divergence times of 39 drosophilid species were studied by using the coding region of the Adh gene. Four genera--Scaptodrosophila, Zaprionus, Drosophila, and Scaptomyza (from Hawaii)--and three Drosophila subgenera--Drosophila, Engiscaptomyza, and Sophophora--were included. After conducting statistical analyses of the nucleotide sequences of the Adh, Adhr (Adh-related gene), and nuclear rRNA genes and a 905-bp segment of mitochondrial DNA, we used Scaptodrosophila as the outgroup. The phylogenetic tree obtained showed that the first major division of drosophilid species occurs between subgenus Sophophora (genus Drosophila) and the group including subgenera Drosophila and Engiscaptomyza plus the genera Zaprionus and Scaptomyza. Subgenus Sophophora is then divided into D. willistoni and the clade of D. obscura and D. melanogaster species groups. In the other major drosophilid group, Zaprionus first separates from the other species, and then D. immigrans leaves the remaining group of species. This remaining group then splits into the D. repleta group and the Hawaiian drosophilid cluster (Hawaiian Drosophila, Engiscaptomyza, and Scaptomyza). Engiscaptomyza and Scaptomyza are tightly clustered. Each of the D. repleta, D. obscura, and D. melanogaster groups is monophyletic. The splitting of subgenera Drosophila and Sophophora apparently occurred about 40 Mya, whereas the D. repleta group and the Hawaiian drosophilid cluster separated about 32 Mya. By contrast, the splitting of Engiscaptomyza and Scaptomyza occurred only about 11 Mya, suggesting that Scaptomyza experienced a rapid morphological evolution. The D. obscura and D. melanogaster groups apparently diverged about 25 Mya. Many of the D. repleta group species studied here have two functional Adh genes (Adh-1 and Adh-2), and these duplicated genes can be explained by two duplication events.
Molecular phylogeny and divergence times of drosophilid species.