Bacterial taxonomy
Bacterial taxonomy is the taxonomy, i.e. the rank-based classification, of bacteria.
In the scientific classification established by Carl von Linné each species has to be assigned to a genus (binary nomenclature), which in turn is a lower level of a hierarchy of ranks (family, suborder, order, subclass, class, division/phyla, kingdom and domain). In the currently accepted classification of Life, 

there are three domains (Eukaryotes, Bacteria and Archaea), which, in terms of taxonomy, despite following the same principles have several different conventions between them and between their subdivisions as are studied by different disciplines (Botany, zoology, mycology and microbiology), for example in zoology there are type specimens, whereas in microbiology there are type strains.
Diversity
Prokaryotes share many common features, such as lack of nuclear membrane, unicellularity, division by binary-fission and generally small size. The various species differ amongst each other based on several characteristics, allowing their identification and classification. Examples include:
·         Phylogeny: All bacteria stem from a common ancestor and diversified since, consequently possess different levels of evolutionary relatedness
·         Metabolism: Different bacteria may have different metabolic abilities (see Microbial metabolism)
·         Environment: Different bacteria thrive in different environments, such as high/low temperature and salt (see Extremophiles)
·         Morphology: There are many structural differences between bacteria, such as cell shape, Gram stain (number of lipid bilayers) or bilayer composition (see Bacterial cellular morphologies, Bacterial cell structure)
·         Pathogenicity: Some bacteria are pathogenic to plants or animals
Classification history
Bacteria were first observed by Antonie van Leeuwenhoek in 1676, using a single-lens microscope of his own design. He called them "animalcules" and published his observations in a series of letters to the Royal Society. The name "bacterium" was introduced much later, by Christian Gottfried Ehrenberg in 1838.
Classical classification
Placement
Tree of Life in Generelle Morphologie der Organismen (1866)

Bacteria were first classified as plants constituting the class Schizomycetes, which along with the Schizophyceae (blue green algae/Cyanobacteria) formed the phylum Schizophyta.
Haeckel in 1866 placed the group in the phylum Moneres (from μονήρης: simple) in the kingdom Protista and defines them as completely structureless and homogeneous organisms, consisting only of a piece of plasma. He subdivided the phylum into two groups:
·         die Gymnomoneren (no envelope)
·         Protogenes—such as Protogenes primordialis, now classed as a eukaryote and not a bacterium
·         Protamaeba—now classed as a eukaryote and not a bacterium
·         Vibrio—a genus of comma shaped bacteria first described in 1854)
·         Bacterium—a genus of rod shaped bacteria first described in 1828, that later gave its name to the members of the Monera, formerly referred to as "a moneron" (plural "monera") in English and "eine Moneren"(fem. plural "Moneres") in German
·         Bacillus—a genus of spore-forming rod shaped bacteria first described in 1835
·         Spirochaeta—thin spiral shaped bacteria first described in 1835
·         Spirillum—spiral shaped bacteria first described in 1832
·         etc.
·         die Lepomoneren (with envelope)
·         Protomonas—now classed as a eukaryote and not a bacterium. The name was reused in 1984 for an unrelated genus of Bacteria
·         Vampyrella—now classed as a eukaryote and not a bacterium
·         The group was later reclassified as the Prokaryotes by Chatton.
·         The classification of Cyanobacteria (colloquially "blue green algae") has been fought between being algae or bacteria (for example, Haeckel classified Nostoc in the phylum Archephyta of Algae).
in 1905 Erwin F. Smith accepted 33 valid different names of bacterial genera and over 150 invalid names,and in 1913 Vuillemin in a study concluded that all species of the Bacteria should fall into the genera Planococcus, Streptococcus, Klebsiella, Merista, Planomerista, Neisseria, Sarcina, Planosarcina, Metabacterium, Clostridium, Serratia, Bacterium and Spirillum.
Ferdinand Cohn recognized 4 tribes: Spherobacteria, Microbacteria, Desmobacteria, and Spirobacteria. Stanier and van Neil recognized the Kingdom Monera with 2 phyla, Myxophyta and Schizomycetae, the latter comprising classes Eubacteriae (3 orders), Myxobacteriae (1 order), and Spirochetae (1 order). Bisset distinguished 1 class and 4 orders: Eubacteriales, Actinomycetales, Streptomycetales, and Flexibacteriales. Migula, which was the most widely accepted system of its time and included all then-known species but was based only on morphology, contained the 3 basic groups, Coccaceae, Bacillaceae, and Spirillaceae but also Trichobacterinae for filamentous bacteria; Orla-Jensen  established 2 orders: Cephalotrichinae (7 families) and Peritrichinae (presumably with only 1 family). Bergey et al presented a classification which generally followed the 1920 Final Report of the SAB(Society of American Bacteriologists) Committee ( Winslow et al), which divided Class Schizomycetes into 4 orders: Myxobacteriales, Thiobacteriales, Chlamydobacteriales, and Eubacteriales, with a 5th group being 4 genera considered intermediate between bacteria and protozoans: Spirocheta, Cristospira, Saprospira, and Treponema.
However, different authors often reclassified the genera due to the lack of visible traits to go by, resulting in a poor state which was summarised in 1915 by Robert Earle Buchanan  By then, the whole group received different ranks and names by different authors namely
·         Schizomycetes (Naegeli 1857
·         Bacteriaceae (Cohn 1872,
·         Bacteria (Cohn 1872b
·         Schizomycetaceae (DeToni and Trevisan 1889,

Furthermore the families, into which the class was subdivided, changed from author to author and for some such as Zipf the names where in German and not in Latin the first edition of the Bacteriological Code in 1947 sorted several problems out.
A.R. Prévot's system had 4 subphyla and 8 classes as follows:
Eubacteriales (classes Asporulales and Sporulales) Mycobacteriales (classes Actinomycetales, Myxobacteriales, and Azotobacteriales) Algobacteriales (classes Siderobacteriales and Thiobacteriales) Protozoobacteriales (class Spirochetales)
Linnaeus
1735
Haeckel
1866
Chatton
1925
Copeland
1938
Whittaker
1969
Woese et al.
1990
Cavalier-Smith
1998
2 kingdoms
3 kingdoms
2 empires
4 kingdoms
5 kingdoms
3 domains
6 kingdoms
(not treated)
Protista
Prokaryota
Monera
Monera
Bacteria
Bacteria
Archaea
Eukaryota
Protoctista
Protista
Eucarya
Protozoa
Chromista
Vegetabilia
Plantae
Plantae
Plantae
Fungi
Fungi
Animalia
Animalia
Animalia
Animalia
Animalia

Subdivisions based on Gram staining
Despite there being little agreement on the major subgroups of the Bacteria, Gram staining results were most commonly used as a classification tool, consequently until the advent of molecular phylogeny, the Kingdom Prokaryotae was divided into four divisions,[39] A classification scheme still formally followed by Bergey's manual of systematic bacteriology for tome order
·         Gracilicutes (gram negative)
·         Photobacteria (photosynthetic): class Oxyphotobacteriae (water as electron acceptor, includes the order Cyanobacteriales=blue green algae, now phylum Cyanobacteria) and class Anoxyphotobacteriae (anaerobic phototrophs, orders: Rhodospirillales and Chlorobiales
·         Scotobacteria (non-photosynthetic, now the Proteobacteria and other gram negative nonphotosynthetic phyla)
·         Firmacutes [sic] (gram positive, subsequently corrected to Fimicutes
·         several orders such as Bacillales and Actinomycetales (now in the phylum Actinobacteria)
·         Mollicutes (gram variable, e.g. Mycoplasma)
·         Mendocutes (uneven gram stain, "methanogenic bacteria" now known as the Archaea)
Molecular era
"Archaic bacteria" and Woese's reclassification
Phylogenetic tree showing the relationship between the archaea and other forms of life. Eukaryotes are colored red, archaea green and bacteria blue. Adapted from Ciccarelli et al.
Woese argued that the bacteria, archaea, and eukaryotes represent separate lines of descent that diverged early on from an ancestral colony of organisms. However, a few biologists argue that the Archaea and Eukaryota arose from a group of bacteria. In any case, it is thought that viruses and archaea began relationships approximately two billion years ago, and that co-evolution may have been occurring between members of these groups. It is possible that the last common ancestor of the bacteria and archaea was a thermophile, which raises the possibility that lower temperatures are "extreme environments" in archaeal terms, and organisms that live in cooler environments appeared only later. Since the Archaea and Bacteria are no more related to each other than they are to eukaryotes, the term prokaryote's only surviving meaning is "not a eukaryote", limiting its value.
With improved methodologies it became clear that the methanogenic bacteria were profoundly different and were (erroneous) believed to be relics of ancient bacteria thus Carl Woese, regarded as the forerunner of the molecular phylogeny revolution, identified three primary lines of descent the Archaebacteria, the Eubacteria and the Urkaryotes, the latter now represented by the nucleocytoplasmic component of the Eukaryotes these lineages were formalised into the rank Domain (regio in Latin) which divided Life into 3 domains: the Eukaryota, the Archaea and the BacteriaThis scheme is still followed today.
Subdivisions
In 1987 Carl Woese divided the Eubacteria into 11 divisions based on 16S ribosomal RNA (SSU) sequences, which with several additions are still used today.
Opposition
While the three domain system is widely accepted, some authors have opposed it for various reasons.
One prominent scientist who opposes the three domain system is Thomas Cavalier-Smith, who proposed that the Archaea and the Eukaryotes (the Neomura) stem from Gram positive bacteria (Posibacteria), which in turn derive from gram negative bacteria (Negibacteria) based on several logical arguments, which are highly controversial and generally disregarded by the molecular biology community (c.f. reviewers' comments on, e.g. Eric Bapteste is "agnostic" regarding the conclusions) and are often not mentioned in reviews (e.g.) due to the subjective nature of the assumptions made.
However, despite there being a wealth of statistically supported studies towards the rooting of the tree of life between the Bacteria and the Neomura by means of a variety of methods,including some that are impervious to accelerated evolution—which is claimed by Cavalier-Smith to be the source of the supposed fallacy in molecular methods there are a few studies which have drawn different conclusions, some of which place the root in the phylum Firmicutes with nested archaea.
Radhey Gupta's molecular taxonomy, based on conserved signature sequences of proteins, includes a monophyletic Gram negative clade, a monophyletic Gram positive clade, and a polyphyletic Archeota derived from Gram positives. Hori and Osawa's molecular analysis indicated a link between Metabacteria (=Archeota) and eukaryotes.The only cladistic analyses for bacteria based on classical evidence largely corroborate Gupta's results (see comprehensive mega-taxonomy).
James Lake presented a 2 primary kingdom arrangement (Parkaryotae + eukaryotes and eocytes + Karyotae) and suggested a 5 primary kingdom scheme (Eukaryota, Eocyta, Methanobacteria, Halobacteria, and Eubactcria) based on ribosomal structure and a 4 primary kingdom scheme (Eukaryota, Eocyta, Methanobacteria, and Photocyta), bacteria being classified according to 3 major biochemical innovations: photosynthesis (Photocyta), methanogenesis (Methanobacteria), and sulfur respiration (Eocyta). He has also discovered evidence that Gram-negative bacteria arose from a symbiosis between 2 Gram-positive bacteria.
Analyses
Bacteria were at first classified based solely on their shape (vibrio, bacillus, coccus etc.), presence of endospores, gram stain, aerobic conditions and motility. This system changed with the study of metabolic phenotypes, where metabolic characteristics were used. Recently, with the advent of molecular phylogeny, several genes are used to identify species, the most important of which is the 16S rRNA gene, followed by 23S, ITS region, gyrB and others to confirm a better resolution. The quickest way to identify to match an isolated strain to a species or genus today is done by amplifying it's 16S gene with universal primers and sequence the 1.4kb amplicon and submit it to a specialised web-based identification database, namely either Ribosomal Database Project, which align the sequence to other 16S sequences using infernal, a secondary structure bases global alignment, or ARB SILVA, which aligns sequences via SINA (SILVA incremental aligner), which does a local alignment of a seed and extends it
Several identification methods exist:
 Phenotypic analyses
·         fatty acid analyses
·         Growth conditions (Agar plate, Biolog multiwell plates)
  Genetic analyses
·         DNA-DNA hybridization
·         DNA profiling
·         Sequence
·         GC ratios
    Phylogenetic analyses
·         16S-based phylogeny
·         phylogeny based on other genes
·         Multi-gene sequence analysis
·         Whole-genome sequence based analysis
New species
The minimal standards for describing a new species depend on which group the species belongs to. c.f.
Candidatus
Candidatus is a component of the taxonomic name for a bacterium that cannot be maintained in a Bacteriology Culture Collection. It is an interim taxonomic status for noncultivable organisms. e.g. "Candidatus Pelagibacter ubique"
Species concept
Bacteria divide asexually and for the most part do not show regionalisms ("Everything is everywhere"), therefore the concept of species, which works best for animals, becomes entirely a matter of judgement
The number of species of bacteria and archaea (approximately 5000) is surprisingly[according to whom?] small considering their early evolution, genetic diversity and residence in all ecosystems. The reason for this is the differences in species concepts between the bacteria and macro-organisms, the difficulties in growing/characterising in pure culture (a prerequisite to naming new species, vide supra) and extensive horizontal gene transfer blurring the distinction of species.
The most commonly accepted definition is the polyphasic species definition, which takes into account both phenotypic and genetic differences. However, a quicker diagnostic ad hoc threshold to separate species is less than 70% DNA-DNA hybridisation, which corresponds to less than 97% 16S DNA sequence identity. It has been noted that if this were applied to animal classification, the order Primates would be a single species.
Pathology vs. phylogeny
Ideally, taxonomic classification should reflect the evolutionary history of the taxa, i.e. the phylogeny. Although some exceptions are present when the phenotype differs amongst the group, especially from a medical standpoint. Some examples of problematic classifications follow.
Escherichia coli: overly large and polyphyletic
In the Enterobacteriaceae family of the class Gammaproteobacteria, the species in the genus Shigella (S. dysenteriae, S. flexneri, S. boydii, S. sonnei) by an evolutionary point of view are strains of the species Escherichia coli (polyphyletic), but due to genetic differences cause different medical conditions in the case of the pathogenic strains. Escherichia coli is a badly classified species as some strains share only 20% of their genome. Being so diverse it should be given a higher taxonomic ranking. However, due to the medical conditions associated with the species, it will not be changed to avoid confusion in medical context.
Bacillus cereus group: close and polyphyletic
In a similar way, the Bacillus species (=phylum Firmicutes) belonging to the "B. cereus group" (B. anthracis, B. cereus, B . thuringiensis, B. mycoides, B. pseudomycoides, B. weihenstephanensis and B. medusa) have 99-100% similar 16S rRNA sequence (97% is a commonly cited adequate species cut-off) and are polyphyletic, but for medical reasons (anthrax etc.) remain separate.
Yersinia pestis: extremely recent species
Yersinia pestis is in effect a strain of Yersinia pseudotuberculosis, but with a pathogenicity island that confer a drastically different pathology (Black plague and tuberculosis-like symptoms respectively) which arose 15,000 to 20,000 years ago.
Nested genera in Pseudomonas
In the gammaproteobacterial order Pseudomonadales, the genus Azotobacter and the species Azomonas macrocytogenes are actually members of the genus Pseudomonas, but were misclassified due to nitrogen fixing capabilities and the large size of the genus Psuedomonas which renders classification problematic. This will probably rectified in the close future.
Nested genera in Bacillus
Another example of a large genus with nested genera is the Bacillus genus, in which the genera Paenibacillus and Brevibacillus are nested clades. There is insufficient genomic data at present to fully and effectively correct taxonomic errors in Bacillus.
Agrobacterium: resistance to name change
Based on molecular data it was shown that the genus Agrobacterium in nested in rhizobium and the Agrobacterium species transferred to the Rhizobium genus (resulting in the following comp. nov.: Rhizobium radiobacter in turn formerly known as A. tumefaciens, R. rhizogenes, R. rubi, R. undicola and R. vitis) Given the plant pathogenic nature of Agrobacterium species, it was proposed to maintain the genus Agrobacterium and the latter was conter-argued
Nomenclature
Taxonomic names are written in italics (or underlined when handwritten) with a majuscule first letter with the exception of epithets for species and subspecies. Despite it being common in zoology, tautonyms (e.g. Bison bison) are not acceptable and names of taxa used in zoology, botany or mycology cannot be reused for Bacteria (Botany and Zoology do share names).
Nomenclature is the set of rules and conventions which govern the names of taxa. The difference in nomenclature between the various kingdoms/domains is reviewed in.
For Bacteria, valid names must have a Latin or Neolatin name and can only use basic latin letters (w and j inclusive, see History of the Latin alphabet for these), consequently hyphens, accents and other letters are not accepted and should be translitterated correctly (e.g. ß=ss). Ancient Greek being written in the Greek alphabet, needs to be translitterated into the Latin alphabet.
When compound words are created, a connecting vowel is needed depending on the origin of the preceding word, regardless of the word that follows, unless the latter starts with a vowel in which case no connecting vowel is added. If the first compound is Latin then the connecting vowel is an -i-, whereas if the first compound is Greek, the connecting vowel is an -o-.
Rules for higher taxa
For for a comparison with other nomenclature codes, see Taxonomic rank#Terminations of names
For the Prokaryotes (Bacteria and Archaea) the rank kingdom is not used (although some authors refer to phyla as kingdoms
If a new or amended species is placed in new ranks, according to Rule 9 of the Bacteriologocal Code the name is formed by the addition of an appropriate suffix to the stem of the name of the type genus. For subclass and class the reccomendation from  is generally followed, resulting in a neutral plural, however a few names do not follow this and instead keep into account graeco-latin grammar (e.g. the female plurals Thermotogae, Aquificae and Chlamydiae, the male plurals Chloroflexi, Bacilli and Deinococci and the greek plurals Spirochaetes, Gemmatimonadetes and Chrysiogenetes).
Rank
Suffix
            Example
Genus

Elusimicrobium
Subtribe (disused)
-inae
(Elusimicrobiinae)
Tribe (disused)
-inae
(Elusimicrobiieae)
Subfamily
-oideae
(Elusimicrobioideae)
Family
-aceae
Elusimicrobiaceae
Suborder
-ineae
(Elusimicrobineae)
Order
-ales
Elusimicrobiales
Subclass
-idae
(Elusimicrobidae)
Class
-ia
Elusimicrobia
Phylum
see text
Elusimicrobia

Phyla endings
Phyla are not covered by the Bacteriological code, however, the scientific community generally follows the Ncbi and Lpsn taxonomy, where the name of the phylum is generally the plural of the type genus, with the exception of the Firmicutes, Cyanobacteria and Proteobacteria, whose names do not stem from a genus name. The higher taxa proposed by Cavalier-Smith are generally disregarded by the molecular phylogeny community (e.g.) (vide supra).
For the Archaea the suffix -archaeota is used. For bacterial phyla it was proposed that the suffix -bacteria be used for phyla.
Consequently for main phyla the name of the phyla is the same as the first described class:
·         Acidobacteria (from Acidobacterium)
·         Actinobacteria (from Actinomyces)
·         Caldisericia (from Caldisericum)
·         Elusimicrobia (from Elusimicrobium)
·         Fusobacteria (from Fusobacterium)
·         Thermodesulfobacteria (from Thermodesulfobacterium)
·         Thermotogae (from Thermotoga)
·         Aquificae (from Aquifica)
·         Chlamydiae (from Chlamydia)
·         Chloroflexi (from Chloroflexus)
·         Chrysiogenetes (from Chrysiogenes)
·         Gemmatimonadetes (from Gemmatimonas)
·         Deferribacteres (from Deferribacter)
Whereas for others where the -ia suffix for class is used regardless of grammar they differ:
·         phylum Bacteroidetes vs. class Bacteroidia from Bacteroides
·         phylum Chlorobi vs. class Chlorobia from Chlorobium
·         phylum Verrucomicrobia vs. class Verrucomicrobiae from Verrucomicrobium (anomalous class name)
·         phylum Dictyoglomi versus class Dictyoglomia from Dictyoglomus
·         phylum Fibrobacteres versus class Fibrobacteria from Fibrobacter (c.f. the suffix -bacter, note the difference with Deferribacteres)
·         phylum Lentisphaerae versus class Lentisphaeria from Lentisphaera
·         phylum Nitrospira or Nitrospirae versus class Nitrospira from Nitrospira
·         phylum Spirochaetes versus class Spirochaetae from Spirochaeta
·         phylum Synergistetes versus class Synergistetia from Synergistes
·         phylum Planctomycetes versus Planctomycea from Planctomyces

An exception is the phylum Deinococcus-Thermus, which bears a hyphenated pair of genera —only non accented latin letters are accepted for valid names, but phyla are not officially recognised.
Names after people
Manynumber? species are named after people, either the discoverer or a famous person in the field of microbiology, for example Salmonella is after D.E. Salmon, who discovered it (albeit as "Bacillus typhi"
For the generic epithet, all names derived from people must be in the female nominative case, either by changing the ending to -a or to the diminutive -ella, depending on the name.
For the specific epithet, the names can be converted into either adjectival form (adding -nus (m.), -na (f.), -num (n.) according to the gender of the genus name) or the genitive of the latinised name.
Names after places
Many species (the specific epithet) are named after the place they are present or found (e.g. Borrelia burgdorferi). Their names are created by forming an adjective by joining the locality's name with the ending -ensis (m. or f.) or ense (n.) in agreement with the gender of the genus name, unless a classical Latin adjective exists for the place. However, names of places should not be used as nouns in the genitive case.
Vernacular names
Despite the fact that some hetero/homogeneus colonies or biofilms of bacteria have names in English (e.g. dental plaque or Star jelly), no bacterial species has a vernacular/trivial/common name in English.
For names in the singular form, plurals cannot be made (singulare tantum) as would imply multiple groups with the same label and not multiple members of that group (by analogy, in English, chairs and tables are types of furniture, which cannot be used in the plural form "furnitures" to describe both members), conversely names plural form are pluralia tantum. However, a partial exception to this is made by the use of vernacular names. However, to avoid repetition of taxonomic names which break the flow of prose, vernacular names of members of a genus or higher taxa are often used and recommended, these are formed by writing the name of the taxa in sentence case roman ("standard" in MS Office) type, therefore treating the proper noun as an English common noun (e.g. the salmonellas), although there is some debate about the grammar of plurals, which can either be regular plural by adding -(e)s (the salmonellas) or using the ancient Greek or Latin plural form (irregular plurals) of the noun (the salmonellae); the latter is problematic as the plural of - bacter would be -bacteres, while the plural of myces (N.L. masc. n. from Gr. masc. n. mukes) is mycetes.
Customs are present for centain names, such as those ending in -monas are converted into -monad (one pseudomonad, two aeromonads and not -monades).
Bacteria which are the etiological cause for a disease are often referred to by the disease name followed by a describing noun (bacterium, bacillus, coccus, agent or the name of their phylum) e.g. cholera bacterium (Vibrio cholera) or Lyme disease spirochete (Borrelia burgdorferi) , note also rickettsialpox (Rickettsia akari)
Treponema is converted into treponeme and the plural is treponemes and not treponemata.
Some unusual bacteria have special names such as Quin's oval (Quinella ovalis) and Walsby's square (Haloquadratum walsbyi).
Before the advent of molecular phylogeny, many higher taxonomic groupings had only trivial names, which are still used today, some of which are polyphyletic, such as Rhizobacteria. Some higher taxonomic trivial names are:

·         Blue-green algae are members of the phylum Cyanobacteria
·         Green non-sulfur bacteria are members of the phylum Chloroflexi
·         Green sulfur bacteria are members of the Chlorobi
·         Purple bacteria are some, but not all, members of the phylum Proteobacteria
·         Purple sulfur bacteria are members of the order Chromatiales
·         low G+C Gram-positive bacteria are members of the phylum Firmicutes, regardless of GC content
·         high G+C Gram-positive bacteria are members of the phylum Actinobacteria, regardless of GC content
·         Rhizobacteria are members of various genera of proteobacteria
·         Rhizobia are members of the order Rhizobiales
·         Lactic streptococci are members of the genus Lactococcus
·         Coryneform bacteria are members of the family Corynebacteriaceae
·         Fruiting gliding bacteria or myxobacteria are members of the order Myxococcales
·         Enterics are members of the order Enterobacteriales, although the term is avoided if they do not live in the intestines, such as Pectobacterium
·         Acetic acid bacteria are members of the family Acetobacteraceae

Terminology
The abbreviation for species is sp. (plural spp.) and is used after a generic epithet to indicate a species of that genus. Often used to denote a strain of a genus for which the species is not known either because has the organism has not been described yet as a species or insufficient tests were conducted to identify it. For example Halomonas sp. GFAJ-1
·         If a bacterium is known and well-studied but not culturable, it is given the term Candidatus in its name
·         A basonym is original name of a new combination, namely the first name given to a taxa before it was reclassified
·         A synonym is an alternative name for a taxa, i.e. a taxa was erroneusly described twice
·         When a taxa is transfer it becomes a new combinations (comb. nov.) or nomina nova (nom. nov.)



·         paraphyly, monophyly and polyphyly
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