Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a3fe7838ee4107b2

Jump to content

Phylum

From Wikipedia, the free encyclopedia

LifeDomainKingdomPhylumClassOrderFamilyGenusSpecies
The hierarchy of biological classification's eight major taxonomic ranks. A kingdom contains one or more phyla. Intermediate minor rankings are not shown.

In biology, a phylum (/ˈf.lʊm/, FYE-luum; pl.: phyla) is a level of classification, or taxonomic rank, that is below kingdom and above class. Traditionally, the term division has been used in botany instead of phylum, although the International Code of Nomenclature for algae, fungi, and plants accepts the terms as equivalent.[1][2][3] Depending on definitions, the animal kingdom Animalia contains about 32 phyla, the plant kingdom Plantae contains about 14 phyla, and the fungus kingdom Fungi contains about eight phyla. Current research in phylogenetics is uncovering the relationships among phyla within larger clades like Ecdysozoa and Embryophyta.

General description

[edit]

The term phylum was coined in 1866 by Ernst Haeckel from the Greek phylon (φῦλον, 'race, stock'), related to phyle (φυλή, 'tribe, clan').[4][5] Haeckel noted that species constantly evolved into new species that seemed to retain few consistent features among themselves and therefore few features that distinguished them as a group ("a self-contained unity"): "perhaps such a real and completely self-contained unity is the aggregate of all species which have gradually evolved from one and the same common original form, as, for example, all vertebrates. We name this aggregate [a] Stamm [i.e., stock / tribe] (Phylon)."[a] In plant taxonomy, August W. Eichler (1883) classified plants into five groups named divisions, a term that remains in use today for groups of plants, algae and fungi.[1][6] The definitions of zoological phyla have changed from their origins in the six Linnaean classes and the four embranchements of Georges Cuvier.[7]

At its most basic, a phylum can be defined in two ways: as a group of organisms with a certain degree of morphological or developmental similarity (the phenetic definition), or a group of organisms with a certain degree of evolutionary relatedness (the phylogenetic definition).[8] Attempting to define a level of the Linnean hierarchy without referring to (evolutionary) relatedness is unsatisfactory, but a phenetic definition is useful when addressing questions of a morphological nature—such as how successful different body plans were.[citation needed]

Definition based on genetic relation

[edit]

The most important objective measure in the above definitions is the "certain degree" that defines how different organisms need to be members of different phyla. The minimal requirement is that all organisms in a phylum should be clearly more closely related to one another than to any other group.[8] Even this is problematic because the requirement depends on knowledge of organisms' relationships: as more data become available, particularly from molecular studies, we are better able to determine the relationships between groups. So phyla can be merged or split if it becomes apparent that they are related to one another or not. For example, the bearded worms were described as a new phylum (the Pogonophora) in the middle of the 20th century, but molecular work almost half a century later found them to be a group of annelids, so the phyla were merged (the bearded worms are now an annelid family).[9] On the other hand, the highly parasitic phylum Mesozoa was divided into two phyla (Orthonectida and Rhombozoa) when it was discovered the Orthonectida are probably deuterostomes and the Rhombozoa protostomes.[10]

This changeability of phyla has led some biologists to call for the concept of a phylum to be abandoned in favour of placing taxa in clades without any formal ranking of group size.[8]

Definition based on body plan

[edit]

A definition of a phylum based on body plan has been proposed by paleontologists Graham Budd and Sören Jensen (as Haeckel had done a century earlier). The definition was posited because extinct organisms are hardest to classify: they can be offshoots that diverged from a phylum's line before the characteristics that define the modern phylum were all acquired. By Budd and Jensen's definition, a phylum is defined by a set of characters shared by all its living representatives.

This approach brings some small problems—for instance, ancestral characters common to most members of a phylum may have been lost by some members. Also, this definition is based on an arbitrary point of time: the present. However, as it is character based, it is easy to apply to the fossil record. A greater problem is that it relies on a subjective decision about which groups of organisms should be considered as phyla.

The approach is useful because it makes it easy to classify extinct organisms as "stem groups" to the phyla with which they bear the most resemblance, based only on the taxonomically important similarities.[8] However, proving that a fossil belongs to the crown group of a phylum is difficult, as it must display a character unique to a sub-set of the crown group.[8] Furthermore, organisms in the stem group of a phylum can possess the "body plan" of the phylum without all the characteristics necessary to fall within it. This weakens the idea that each of the phyla represents a distinct body plan.[11]

A classification using this definition may be strongly affected by the chance survival of rare groups, which can make a phylum much more diverse than it would be otherwise.[12]

Known phyla

[edit]

Animals

[edit]

Total numbers are estimates; figures from different authors vary wildly, not least because some are based on described species,[13] and some on extrapolations to numbers of undescribed species. For instance, around 25,000–27,000 species of nematodes have been described, while published estimates of the total number of nematode species include 10,000–20,000; 500,000; 10 million; and 100 million.[14]

Lophotrochozoa

Platytrochozoa Spiralia Protostomia Nephrozoa

Mesozoa, Rouphozoa, etc.

Gnathifera

Ecdysozoa

Deuterostomia

Basal

Phylum Meaning Common name Distinguishing characteristic Number of living species described Number of extinct species described
Agmata Fragmented Conical shells with angled layers of sediment (laminae), and a thin hollow tube running through the center None 4–9
Annelida Little ring [15]:306 Segmented worms, annelids No single characteristic shared among all species[16] 22000+[citation needed]
Arthropoda Jointed foot Arthropods Chitinous cuticle, and, at some life stage or sex, internal segmentation (only embryonic for most Acari), and segmented appendages 1250000+[17] 20000+ [citation needed]
Brachiopoda Arm foot[15]:336 Lampshells[15]:336 True lophophore and pedicle ~300–500[citation needed] 12000+ [citation needed]
Bryozoa (Ectoprocta) Moss animals Moss animals, sea mats, ectoprocts[15]:332 True lophophore, multiciliated epithelium and destructive metamorphosis ~6000[17]
Chaetognatha Longhair jaw Arrow worms[15]:342 Chitinous spines either side of head and the corona ciliata ~100[citation needed]
Chordata With a cord Chordates Hollow dorsal nerve cord, notochord, and endostyle ~55000[17]
Cnidaria Stinging nettle Cnidarians Cnidocyte production ~16000[17]
Ctenophora Comb bearer Comb jellies[15]:256 Eight longitudinal rows of plate-shaped fused groups of cilia ~100–150[citation needed] 15–26[18]
Cycliophora Wheel carrying Wheel wearers Chordoid organ and larvae, Prometheus larvae and their multiple-male injection, and Pandora larvae 2 None
Dicyemida Lozenge animal Dicyemids Infusoriform larvae, inner axial cell covered by ciliated peripheral cells in vermiform stages, emperipolesis of agametes into the axial cell of the vermiform stages,[19] of the first spermatogonium into the infusorigen axial cell,[20] and of germ line cells into the urn cells during infusoriform embryo formation[21] 100+[citation needed] None
Echinodermata Spiny skin Echinoderms[15]:348 Tube feet, mesodermal stereom ossicles, catch connective tissue, water vascular system ~7500[17] ~13000 [citation needed]
Entoprocta Inside anus[15]:292 Goblet worms Anus positioned within lophophore-like organ and no coelom ~150[citation needed] 1[22]
Gastrotricha Hairy stomach[15]:288 Hairybellies Posterior tubules with adhesive and detaching glands without anchor cells[23] ~690[citation needed]
Gnathostomulida Jaw orifice Jaw worms[15]:260 Monociliated epidermis (also in some gastrotrichs, e.g. Chordodasys, Xenodasys[24]), unique jaws (absent in Agnathiella[25]) without manubria (also absent in some rotifers, e.g. Acanthocephala) or homologous elements[26] and a 5-part unpaired "basal plate"[27] (absent in some genera) without a "manus",[26] and occipitalia (possibly absent in Problognathia minima and an undescribed species and genus[28]) ~100[citation needed]
Hemichordata Half cord[15]:344 Hemichordates Stomochord, three-part body with proboscis/head shield, collar, and trunk, each section with a separate coelom ~130[citation needed] 8–11 non-graptolites, [29][30][31][32][33][34] ~8400 graptolites[35]
Kinorhyncha Motion snout Mud dragons Presence of both metamerism and scalids ~150[citation needed] 2[36]
Loricifera Armour bearer Brush heads, corset animals Higgins larvae, clavoscalids, spinoscalids with individual intrinsic musculature, protonephridia within gonads in adult ~122[citation needed] 2–3[37]
Micrognathozoa Tiny jaw animals 18 pairs of trunk ciliophores[38] 2 None
Mollusca Soft[15]:320 Mollusks, molluscs Mantle, foot (or its precursors or derived structures), radula (absent in bivalves), ctenidia (sometimes absent)[39]:522 85000+[17] 80000+[40]
Monoblastozoa

(Nomen inquirendum)

One sprout animals Single layer of cells (monoblastic) and through-gut (i.e. anus and mouth), meaning that the cells contact both the internal digestive cavity and external ambient. 1 None
Nematoda Thread like Roundworms, threadworms, eelworms, nematodes[15]:274 Tripartite collagenous cuticle, exclusively longitudinal body-wall musculature (also in Nematomorpha), amphids 25,000[17]
Nematomorpha Thread form[15]:276 Horsehair worms, Gordian worms[15]:276 Mostly subpharyngeal brain, unique larva[41] ~320[citation needed]
Nemertea A sea nymph[15]:270 Ribbon worms[15]:270 Proboscis and rhynchocoel (except in Arhynchonemertes) ~1200[citation needed]
Onychophora Claw bearer Velvet worms[15]:328 Sperm with a subplasmalemmal manchette, nine accessory microtubules surrounding the axoneme, an annulus inside the neck region and an extracellular helical band of secretion surrounding the head[42] ~200[citation needed]
Orthonectida Straight swimmer Orthonectids Embryonic development undergoes inside a plasmodium,[43]:13 adults made up only of a simple nervous and muscular system,[43]:13 internal reproductive cells,[43]:13 which are gonochoric (with the exception of Stoecharthrum,[43]:11 and, possibly, Pelmatosphaera[44]), and external cells alternating in rings, of 1–3 cell rows,[43]:13 of ciliated and unciliated cells[43]:13 (except in Stoecharthrum, where cells after ring 22 are all ciliated,[45] and Pelmatosphaera, where all cells are ciliated[44][46]) ~20[citation needed]
Petalonamae Shaped like leaves Petalonamids, frondomorphs, fronds Glide symmetry (on petalodium) without subset radial symmetry (as in sea pens), and sessility
Phoronida Zeus's mistress Horseshoe worms Body composed of an anterior epistome (prosome), middle lophophore (mesosome), and a posterior trunk (metasome) that has a single pair of metanephridia, tipped with an end bulb (ampulla), actinotroch larva (except in Phoronis ovalis)[39]:638–644 11[citation needed]
Placozoa Plate animals Trichoplaxes, placozoans[15]:242 Minute, asymmetrical, flattened body, "shiny spheres"[39]:215 4 (5 if Treptoplax is valid) Possibly 1[47][48]
Platyhelminthes Flat worm[15]:262 Flatworms[15]:262 Non-mitotic epidermal cells, replaced by kinetosome-containing cells that originate in the parenchyma,[49] no coelom, protonephridia present[39]:376 ~2950[17]
Porifera Pore bearer Sponges[15]:246 Choanocytes (absent in some Cladorhizidae),[50] mesohyl, pinacocytes (latter and possibly former absent in Hexactinellida),[51] archeocytes (possibly exclusive to Demospongiae,[52] otherwise, absent in all Calcarea[52]:28 and some Homoscleromorpha[53][54]:13), spicules (many demosponges and homosclerans lack them, e.g. Halisarca and Oscarella, respectively[39]:220), no basal lamina[39]:246 (except Homoscleromorpha[55]), nervous or muscle cells[56] (also absent in Placozoa,[56] Myxosporea,[57] (vermiform stages of Malacosporea do have muscles[58]), and Dicyemida[59]) 10800[17]
Priapulida Little Priapus Penis worms Introvert with scalids but no trichoscalids ~20[citation needed]
Proarticulata Before articulates External glide symmetry and motility None 25[citation needed]
Rotifera Wheel bearer Rotifers,[15]:282 wheel animals, wheel animalcules Corona (sometimes unciliated, e.g. Cupelopagis), "foot" with "toes" and adhesive glands (sometimes absent, e.g. Keratella[60]) (possibly homologous with acanthocephalan cement glands[61]), trophi (sometimes absent, e.g. Acanthocephala,[62] male Asplanchna[63]), intracytoplasmic laminae (also in Micrognathozoa[64])[39]:618 ~3500[17]
Saccorhytida Saccus: "pocket" and "wrinkle" Saccorhytids Microscopic, ellipsoidal body shape with pronounced bilateral symmetry expressed by paired spiny sclerites. Single, presumably oral opening on assumed ventral side (no anus).[65] None 2[66][67]
Tardigrada Slow step Water bears, moss piglets Outer connectives (secondary connection between protocerebrum and first ventral trunk ganglion)[68][39]:711,717 ~1000 3[69]
Trilobozoa Three-lobed animal Trilobozoans Flattened and triradially symmetrical None
Vetulicolia Ancient dweller Vetulicolians Laterally compressed pelagic animals with gill slits and the anus located at the apex of the segmented tail None 17[citation needed]
Xenacoelomorpha Strange hollow form Xenacoelomorphs, xenacoels, xenacoelans Bilateral symmetry and no nephridia or protonephridia, pulsatile bodies, "xenacoelomorphan cilia" (standard 9+2 microfilament arrangement, except doublets 4–6 fail to reach the end of the cilium)[39]:346 400+[citation needed]
Total: 39 1,525,000[17]

Plants

[edit]

The kingdom Plantae is defined in various ways by different biologists (see Current definitions of Plantae). All definitions include the living embryophytes (land plants), to which may be added the two green algae divisions, Chlorophyta and Charophyta, to form the clade Viridiplantae. The table below follows the influential (though contentious) Cavalier-Smith system in equating "Plantae" with Archaeplastida,[70] a group containing Viridiplantae and the algal Rhodophyta and Glaucophyta divisions.

The definition and classification of plants at the division level also varies from source to source, and has changed progressively in recent years. Thus some sources place horsetails in division Arthrophyta and ferns in division Monilophyta,[71] while others place them both in Monilophyta, as shown below. The division Pinophyta may be used for all gymnosperms (i.e. including cycads, ginkgos and gnetophytes),[72] or for conifers alone as below.

Since the first publication of the APG system in 1998, which proposed a classification of angiosperms up to the level of orders, many sources have preferred to treat ranks higher than orders as informal clades. Where formal ranks have been provided, the traditional divisions listed below have been reduced to a very much lower level, e.g. subclasses.[73]

Archaeplastida Biliphyta[70] Other algae
Viridiplantae Green algae
Embryophyte (Land plants)
DivisionMeaningCommon nameDistinguishing characteristicsSpecies described
Anthocerotophyta[74] Anthoceros-like plants Hornworts Horn-shaped sporophytes, no vascular system 100–300+
Bryophyta[74] Bryum-like plants, moss plants Mosses Persistent unbranched sporophytes, no vascular system approx. 12,000
Charophyta Chara-like plants Charophytes approx. 1,000
Chlorophyta (Yellow-)green plants[75]:200 Chlorophytes approx. 7,000
Cycadophyta[76] Cycas-like plants, palm-like plants Cycads Seeds, crown of compound leaves approx. 100–200
Ginkgophyta[77] Ginkgo-like plants Ginkgophytes Seeds not protected by fruit only 1 extant; 50+ extinct
Glaucophyta Blue-green plants Glaucophytes 15
Gnetophyta[78] Gnetum-like plants Gnetophytes Seeds and woody vascular system with vessels approx. 70
Lycophyta[79] Lycopodium-like plants

Wolf plants

Clubmosses Microphyll leaves, vascular system 1,290 extant
Angiospermae Seed container Flowering plants, angiosperms Flowers and fruit, vascular system with vessels 300,000
Marchantiophyta,[80]

Hepatophyta[74]

Marchantia-like plants

Liver plants

Liverworts Ephemeral unbranched sporophytes, no vascular system approx. 9,000
Polypodiophyta Polypodium-like plants
Ferns Megaphyll leaves, vascular system approx. 10,560
Picozoa Extremely small animals Picozoans, picobiliphytes 1
Pinophyta,[72]

Coniferophyta[81]

Pinus-like plants

Cone-bearing plant

Conifers Cones containing seeds and wood composed of tracheids 629 extant
Prasinodermophyta Prasinoderma-like plants Picozoans, picobiliphytes, biliphytes 8
Rhodophyta Red plants Red algae Use phycobiliproteins as accessory pigments. approx. 7,000
Total: 16

Fungi

[edit]
DivisionMeaningCommon nameDistinguishing characteristicsSpecies described
Ascomycota Bladder fungus[75]:396 Ascomycetes,[75]:396 sac fungi Tend to have fruiting bodies (ascocarp).[82] Filamentous, producing hyphae separated by septa. Can reproduce asexually. 30,000
Basidiomycota Small base fungus[75]:402 Basidiomycetes,[75]:402 club fungi Bracket fungi, toadstools, smuts and rust. Sexual reproduction.[citation needed] 31,515
Blastocladiomycota Offshoot branch fungus[83] Blastoclads Less than 200
Chytridiomycota Little cooking pot fungus[84] Chytrids Predominantly Aquatic saprotrophic or parasitic. Have a posterior flagellum. Tend to be single celled but can also be multicellular.[85][86][87] 1000+
Glomeromycota Ball of yarn fungus[75]:394 Glomeromycetes, AM fungi[75]:394 Mainly arbuscular mycorrhizae present, terrestrial with a small presence on wetlands. Reproduction is asexual but requires plant roots. 284
Microsporidia Small seeds[88] Microsporans[75]:390 1400
Neocallimastigomycota New beautiful whip fungus[89] Neocallimastigomycetes Predominantly located in digestive tract of herbivorous animals. Anaerobic, terrestrial and aquatic.[90] approx. 20 [91]
Zygomycota Pair fungus[75]:392 Zygomycetes[75]:392 Most are saprobes and reproduce sexually and asexually.[90] approx. 1060
Total: 8

Phylum Microsporidia is generally included in kingdom Fungi, though its exact relations remain uncertain,[92] and it is considered a protozoan by the International Society of Protistologists[93] (see Protista, below). Molecular analysis of Zygomycota has found it to be polyphyletic (its members do not share an immediate ancestor),[94] which is considered undesirable by many biologists. Accordingly, there is a proposal to abolish the Zygomycota phylum. Its members would be divided between phylum Glomeromycota and four new subphyla incertae sedis (of uncertain placement): Entomophthoromycotina, Kickxellomycotina, Mucoromycotina, and Zoopagomycotina.[92]

Protists

[edit]

The kingdom Protista (or Protoctista) is included in the traditional five- or six-kingdom model, where it can be defined as containing all eukaryotes that are not plants, animals, or fungi.[75]:120 Protista is a paraphyletic taxon,[95] which is less acceptable to present-day biologists than in the past. Proposals have been made to divide it among several new kingdoms, such as Protozoa and Chromista in the Cavalier-Smith system.[96]

Protist taxonomy has long been unstable,[97] with different approaches and definitions resulting in many competing classification schemes. Many of the phyla listed below are used by the Catalogue of Life,[98] and correspond to the Protozoa-Chromista scheme,[93] with updates from the latest (2022) publication by Cavalier-Smith.[99] Other phyla are used commonly by other authors, and are adapted from the system used by the International Society of Protistologists (ISP). Some of the descriptions are based on the 2019 revision of eukaryotes by the ISP.[100]

Stramenopiles Diaphoretickes
Alveolata
Rhizaria
"Hacrobia"
Amorphea
Excavates
Orphan groups
PhylumMeaningCommon nameDistinguishing characteristicsSpecies describedImage
Amoebozoa Amorphous animals Amoebozoans Presence of pseudopodia for amoeboid movement, tubular cristae.[100] approx. 2,400[101]
Apicomplexa Apical infolds[102] Apicomplexans, sporozoans Mostly parasitic, at least one stage of the life cycle with flattened subpellicular vesicles and a complete apical complex, non-photosynthetic apicoplast.[100] over 6,000[102]
Apusozoa
(paraphyletic)
Apusomonas-like animals Gliding biciliates with two or three connectors between centrioles 32
Bigyra Two rings Stramenopiles with a double helix in ciliary transition zone
Cercozoa Flagellated animal Cercozoans Defined by molecular phylogeny, lacking distinctive morphological or behavioural characters.[100]
Chromerida Chromera-like organisms Chrompodellids, chromerids, colpodellids[103] Biflagellates, chloroplasts with four membranes, incomplete apical complex, cortical alveoli, tubular cristae.[100] 8[104]
Choanozoa
(paraphyletic)
Funnel animals[75] Opisthokont protists Filose pseudopods; some with a colar of microvilli surrounding a flagellum approx. 300[101]
Ciliophora Cilia bearers Ciliates Presence of multiple cilia and a cytostome. approx. 4,500[105]
Cryptista Hidden[75] Defined by molecular phylogeny, flat cristae.[100] 246[104][100]
Dinoflagellata Whirling flagellates[75] Dinoflagellates Biflagellates with a transverse ribbon-like flagellum with multiple waves beating to the cell's left and a longitudinal flagellum beating posteriorly with only one or few waves.[100] 2,957 extant
955 fossil[104]
Endomyxa Within mucus[75][106] Defined by molecular phylogeny,[100] typically plasmodial endoparasites of other eukaryotes.[106]
Eolouka
(paraphyletic)
Early groove[107] Heterotrophic biflagellates with ventral feeding groove.[107] 23
Euglenozoa True eye animals Biflagellates, one of the two cilia inserted into an apical or subapical pocket, unique ciliary configuration.[100] 2,037 extant
20 fossil[104]
Haptista Fasten[75] Thin microtubule-based appendages for feeding (haptonema in haptophytes, axopodia in centrohelids), complex mineralized scales.[100] 517 extant
1,205 fossil[104]
Hemimastigophora Incomplete or atypical flagellates[108] Hemimastigotes[109] Ellipsoid or vermiform phagotrophs, two slightly spiraling rows of around 12 cilia each, thecal plates below the membrane supported by microtubules and rotationally symmetrical, tubular and saccular cristae.[100][108] 10[110]
Heterolobosea;[111]
Percolozoa
Percolomonas-like animals Heteroloboseans, amoebomastigotes[75] Complex life cycle containing amoebae, flagellates and cysts.[100] Amoeboflagellates with an amoeba, a flagellate, and a cyst stage in their life cycles. Amoebae usually cylindrical, with a monopodial locomotive form, relatively fast-moving via eruptive lobopodia. Flagellates usually with two or four flagella that arise at the anterior end of a feeding groove. Golgi apparatus lacking a classic stacked form. Mitochondria with discoidal cristae, some species with acristate, hydrogen-producing mitochondrion-related organelles.[111] approx. 170[111]
Malawimonada Malawimonas-like organisms Malawimonads Small free-living bicilates with two kinetosomes, one or two vanes in posterior cilium. 3[112]
Metamonada Middle monads Metamonads Anaerobic or microaerophilic, some without mitochondria; four kinetosomes per kinetid
Ochrophyta;
Heterokontophyta
Ochre plants, heterokont plants Heterokont algae, stramenochromes, ochrophytes, heterokontophytes Biflagellates with tripartite mastigonemes, chloroplasts with four membranes and chlorophylls a and c, tubular cristae.[100] 21,052 extant
2,262 fossil[104]
Opisthosporidia
(often considered fungi)
Opisthokont spores[113] Parasites with chitinous spores and extrusive host-invasion apparatus
Perkinsozoa Perkinsus-like animals Perkinsozoans, perkinsids Parasitic biflagellates, incomplete apical complex, formation of zoosporangia or undifferentiated cells via a hypha-like tube.[100] 26
Provora Devouring voracious protists[114] Defined by molecular phylogeny, free-living eukaryovorous heterotrophic biflagellates with ventral groove and extrusomes.[114] 7[114]
Pseudofungi False fungi Defined by molecular phylogeny, phagotrophic heterokonts with a helical ciliary transition zone.[115] over 1,200[116]
Retaria Reticulopodia-bearing organisms[106] Feeding by reticulopodia (or axopodia) typically projected through various types of skeleton, closed mitosis.[117] 10,000 extant
50,000 fossil
Sulcozoa
(paraphyletic)
Groove-bearing animals[107] Aerobic flagellates (none, 1, 2 or 4 flagella) with dorsal semi-rigid pellicle of one or two submembrane dense layers, ventral feeding groove, branching ventral pseudopodia, typically filose.[107] 40+
Telonemia Telonema-like organisms[118] Telonemids[119] Phagotrophic pyriform biflagellates with a unique complex cytoskeleton, tubular cristae, tripartite mastigonemes, cortical alveoli.[118][119] 7
Total: 26, but see below.

The number of protist phyla varies greatly from one classification to the next. The Catalogue of Life includes Rhodophyta and Glaucophyta in kingdom Plantae,[98] but other systems consider these phyla part of Protista.[120] In addition, less popular classification schemes unite Ochrophyta and Pseudofungi under one phylum, Gyrista, and all alveolates except ciliates in one phylum Myzozoa, later lowered in rank and included in a paraphyletic phylum Miozoa.[99] Even within a phylum, other phylum-level ranks appear, such as the case of Bacillariophyta (diatoms) within Ochrophyta. These differences became irrelevant after the adoption of a cladistic approach by the ISP, where taxonomic ranks are excluded from the classifications after being considered superfluous and unstable. Many authors prefer this usage, which lead to the Chromista-Protozoa scheme becoming obsolete.[100]

Bacteria

[edit]

Currently there are 41 bacterial phyla (not including "Cyanobacteria") that have been validly published according to the Bacteriological Code[121]

  1. Abditibacteriota
  2. Acidobacteriota, phenotypically diverse and mostly uncultured
  3. Actinomycetota, High-G+C Gram positive species
  4. Aquificota, deep-branching
  5. Armatimonadota
  6. Atribacterota
  7. Bacillota, Low-G+C Gram positive species, such as the spore-formers Bacilli (aerobic) and Clostridia (anaerobic)
  8. Bacteroidota
  9. Balneolota
  10. Bdellovibrionota
  11. Caldisericota, formerly candidate division OP5, Caldisericum exile is the sole representative
  12. Calditrichota
  13. Campylobacterota
  14. Chlamydiota
  15. Chlorobiota, green sulphur bacteria
  16. Chloroflexota, green non-sulphur bacteria
  17. Chrysiogenota, only 3 genera (Chrysiogenes arsenatis, Desulfurispira natronophila, Desulfurispirillum alkaliphilum)
  18. Coprothermobacterota
  19. Deferribacterota
  20. Deinococcota, Deinococcus radiodurans and Thermus aquaticus are "commonly known" species of this phyla
  21. Dictyoglomota
  22. Elusimicrobiota, formerly candidate division Thermite Group 1
  23. Fibrobacterota
  24. Fusobacteriota
  25. Gemmatimonadota
  26. Ignavibacteriota
  27. Kiritimatiellota
  28. Lentisphaerota, formerly clade VadinBE97
  29. Mycoplasmatota, notable genus: Mycoplasma
  30. Myxococcota
  31. Nitrospinota
  32. Nitrospirota
  33. Planctomycetota
  34. Pseudomonadota, the most well-known phylum, containing species such as Escherichia coli or Pseudomonas aeruginosa
  35. Rhodothermota
  36. Spirochaetota, species include Borrelia burgdorferi, which causes Lyme disease
  37. Synergistota
  38. Thermodesulfobacteriota
  39. Thermomicrobiota
  40. Thermotogota, deep-branching
  41. Verrucomicrobiota

Archaea

[edit]

Currently there are 5 phyla that have been validly published according to the Bacteriological Code[121]. There were many changes to the phyla and the names used for them in 2023.[122]

  1. Methanobacteriota, a phylum including a range of archaeans, including methanogens and halophilic archaea (halobacteria), according to LPSN. Previously called Euryarchaeota [122]
  2. Microcaldota (previously known as Ca. Micrarchaeota)[123]
  3. Nanodellota (previously Nanoarchaeota [122]
  4. Promethearchaeota (phylum within the kingdom Promethearchaeati, which was previously known as Asgard Archaea), thought to include the ancestor of Eukaryotes.[124]
  5. Thermoproteota, second most common archaeal phylum (previously known as Crenarchaeota)[125]

[126]

Other phyla that have been proposed, but not validly named, include:

  1. "Euryarchaeota", most common archaeal phylum
  2. "Korarchaeota"
  3. "Nanoarchaeota", ultra-small symbiotes, single known species

See also

[edit]

Notes

[edit]
  1. "Wohl aber ist eine solche reale und vollkommen abgeschlossene Einheit die Summe aller Species, welche aus einer und derselben gemeinschaftlichen Stammform allmählig sich entwickelt haben, wie z. B. alle Wirbelthiere. Diese Summe nennen wir Stamm (Phylon)."

References

[edit]
  1. 1 2 McNeill, J.; et al., eds. (2012). International Code of Nomenclature for algae, fungi, and plants (Melbourne Code), Adopted by the Eighteenth International Botanical Congress Melbourne, Australia, July 2011 (electronic ed.). International Association for Plant Taxonomy. Archived from the original on 10 October 2020. Retrieved 14 May 2017.
  2. "Life sciences". The American Heritage New Dictionary of Cultural Literacy (third ed.). Houghton Mifflin Company. 2005. Retrieved 4 October 2008. Phyla in the plant kingdom are frequently called divisions.
  3. Berg, Linda R. (2 March 2007). Introductory Botany: Plants, People, and the Environment (2 ed.). Cengage Learning. p. 15. ISBN 978-0-534-46669-5. Retrieved 23 July 2012.
  4. Valentine, James W. (2004). On the Origin of Phyla. Chicago: University of Chicago Press. p. 8. ISBN 978-0-226-84548-7.
  5. Haeckel, Ernst (1866). Generelle Morphologie der Organismen [The General Morphology of Organisms] (in German). Vol. 1. Berlin, (Germany): G. Reimer. pp. 28–29.
  6. Naik, V. N. (1984). Taxonomy of Angiosperms. Tata McGraw-Hill. p. 27. ISBN 978-0-07-451788-8.
  7. Collins AG, Valentine JW (2001). "Defining phyla: evolutionary pathways to metazoan body plans". Evolution and Development. 3 (6): 432–442. Bibcode:2001EvDev...3..432C. doi:10.1046/j.1525-142X.2001.01048.x. PMID 11806639. Archived from the original (PDF) on 27 April 2020. Retrieved 5 March 2013.
  8. 1 2 3 4 5 Budd, G. E.; Jensen, S. (May 2000). "A critical reappraisal of the fossil record of the bilaterian phyla". Biological Reviews. 75 (2): 253–295. Bibcode:2000BioRv..75..253B. doi:10.1111/j.1469-185X.1999.tb00046.x. PMID 10881389. S2CID 39772232. Archived from the original on 15 September 2019. Retrieved 26 May 2007.
  9. Rouse, G. W. (2001). "A cladistic analysis of Siboglinidae Caullery, 1914 (Polychaeta, Annelida): formerly the phyla Pogonophora and Vestimentifera". Zoological Journal of the Linnean Society. 132 (1): 55–80. doi:10.1006/zjls.2000.0263.
  10. Pawlowski J, Montoya-Burgos JI, Fahrni JF, Wüest J, Zaninetti L (October 1996). "Origin of the Mesozoa inferred from 18S rRNA gene sequences". Molecular Biology and Evolution. 13 (8): 1128–32. doi:10.1093/oxfordjournals.molbev.a025675. PMID 8865666.
  11. Budd, G. E. (September 1998). "Arthropod body-plan evolution in the Cambrian with an example from anomalocaridid muscle". Lethaia. 31 (3): 197–210. Bibcode:1998Letha..31..197B. doi:10.1111/j.1502-3931.1998.tb00508.x.
  12. Briggs, D. E. G.; Fortey, R. A. (2005). "Wonderful strife: systematics, stem groups, and the phylogenetic signal of the Cambrian radiation". Paleobiology. 31 (2 (Suppl)): 94–112. doi:10.1666/0094-8373(2005)031[0094:WSSSGA]2.0.CO;2. S2CID 44066226.
  13. Zhang, Zhi-Qiang (30 August 2013). "Animal biodiversity: An update of classification and diversity in 2013. In: Zhang, Z.-Q. (Ed.) Animal Biodiversity: An Outline of Higher-level Classification and Survey of Taxonomic Richness (Addenda 2013)". Zootaxa. 3703 (1): 5. doi:10.11646/zootaxa.3703.1.3.
  14. Felder, Darryl L.; Camp, David K. (2009). Gulf of Mexico Origin, Waters, and Biota: Biodiversity. Texas A&M University Press. p. 1111. ISBN 978-1-60344-269-5.
  15. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 Margulis, Lynn; Chapman, Michael J. (2009). Kingdoms and Domains: An Illustrated Guide to the Phyla of Life on Earth (4th corrected ed.). London: Academic Press. ISBN 978-0-12-373621-5.
  16. Purschke, Günter; Bleidorn, Christoph; Struck, Torsten (2014). "Systematics, evolution and phylogeny of Annelida – a morphological perspective". Memoirs of Museum Victoria. 71: 247–269. doi:10.24199/j.mmv.2014.71.19.
  17. 1 2 3 4 5 6 7 8 9 10 11 Zhang, Zhi-Qiang (30 August 2013). "Animal biodiversity: An update of classification and diversity in 2013. In: Zhang, Z.-Q. (Ed.) Animal Biodiversity: An Outline of Higher-level Classification and Survey of Taxonomic Richness (Addenda 2013)". Zootaxa. 3703 (1): 5. doi:10.11646/zootaxa.3703.1.3.
  18. Moroz, Leonid L.; Collins, Richard; Paulay, Gustav (2024), Moroz, Leonid L. (ed.), "Ctenophora: Illustrated Guide and Taxonomy", Ctenophores, vol. 2757, New York, NY: Springer US, pp. 27–102, doi:10.1007/978-1-0716-3642-8_2, ISBN 978-1-0716-3641-1, retrieved 28 August 2026{{citation}}: CS1 maint: work parameter with ISBN (link)
  19. Furuya, Hidetaka; Tsuneki, Kazuhiko (May 2003). "Biology of Dicyemid Mesozoans". Zoological Science. 20 (5): 519–532. doi:10.2108/zsj.20.519. ISSN 0289-0003.
  20. Furuya, Hidetaka; Tsuneki, Kazuhiko (2007). "Developmental patterns of the hermaphroditic gonad in dicyemid mesozoans (Phylum Dicyemida)". Invertebrate Biology. 126 (4): 295–306. doi:10.1111/j.1744-7410.2007.00100.x. ISSN 1744-7410.
  21. Furuya, H.; Tsuneki, K.; Koshida, Y. (October 1992). "Development of the Infusoriform Embryo of Dicyema japonicum (Mesozoa: Dicyemidae)". The Biological Bulletin. 183 (2). The University of Chicago Press: 248–257. doi:10.2307/1542212.
  22. Hou, Xian‐guang; Siveter, David J.; Siveter, Derek J.; Aldridge, Richard J.; Cong, Pei‐yun; Gabbott, Sarah E.; Ma, Xiao‐ya; Purnell, Mark A.; Williams, Mark (12 April 2017). The Cambrian Fossils of Chengjiang, China: The Flowering of Early Animal Life (1 ed.). Wiley. doi:10.1002/9781118896372. ISBN 978-1-118-89638-9.
  23. Tyler, Seth; Rieger, Gunde E. (February 1980). "Adhesive organs of the gastrotricha: I. Duo-gland organs". Zoomorphologie. 95 (1): 1–15. doi:10.1007/BF01342230. ISSN 0340-6725.
  24. Møbjerg Kristensen, Reinhardt; Funch, Peter (2000). "Micrognathozoa: A new class with complicated jaws like those of Rotifera and Gnathostomulida". Journal of Morphology (in French). 246 (1): 1–49. doi:10.1002/1097-4687(200010)246:1<1::AID-JMOR1>3.0.CO;2-D. ISSN 1097-4687.
  25. Sterrer, Wolfgang (January 1971). "Agnathiella beckeri nov. gen. nov. spec, from Southern Florida: The First Gnathostomulid Without Jaws". Internationale Revue der gesamten Hydrobiologie und Hydrographie. 56 (2): 215–225. doi:10.1002/iroh.19710560204. ISSN 0020-9309.
  26. 1 2 Sørensen, Martin Vinther (February 2003). "Further structures in the jaw apparatus of limnognathia maerski (micrognathozoa), with notes on the phylogeny of the gnathifera". Journal of Morphology. 255 (2): 131–145. doi:10.1002/jmor.10038. ISSN 0362-2525.
  27. Sørensen, Martin Vinther (2003). "Further structures in the jaw apparatus of limnognathia maerski (micrognathozoa), with notes on the phylogeny of the gnathifera". Journal of Morphology. 255 (2): 131–145. doi:10.1002/jmor.10038. ISSN 1097-4687.
  28. Sørensen, Martin V.; Sterrer, Wolfgang; Giribet, Gonzalo (2006). "Gnathostomulid phylogeny inferred from a combined approach of four molecular loci and morphology". Cladistics. 22 (1): 32–58. doi:10.1111/j.1096-0031.2006.00085.x. ISSN 1096-0031.
  29. Maletz, Jörg; Gonzalez, Paul (15 February 2017). "Treatise Online no. 100: Part V, Second Revision, Chapter 14: Order Cephalodiscida: Introduction and systematic descriptions". Treatise Online. doi:10.17161/to.v0i0.6674. ISSN 2153-4012.
  30. Abrard, Rene; Ph. Dollfus, Robert; Soyer, Robert (1 January 1950). "Tubes silicifies presumes de Cephalodiscus, dans le Lutetien lagunaire de la region parisienne". Bulletin de la Société Géologique de France. S5-XX (1–3): 51–55. doi:10.2113/gssgfbull.S5-XX.1-3.51. ISSN 0037-9409.
  31. Briggs, Derek E.G.; Mongiardino Koch, Nicolás (December 2023). "A Silurian pseudocolonial pterobranch". Current Biology. 33 (23): 5225–5232.e3. doi:10.1016/j.cub.2023.10.024.
  32. Maletz, Jörg (15 March 2014). "Hemichordata (Pterobranchia, Enteropneusta) and the fossil record". Palaeogeography, Palaeoclimatology, Palaeoecology. Cambrian Bioradiation. 398: 16–27. doi:10.1016/j.palaeo.2013.06.010. ISSN 0031-0182.
  33. Nanglu, Karma; Caron, Jean-Bernard; Cameron, Christopher B. (November 2020). "Cambrian Tentaculate Worms and the Origin of the Hemichordate Body Plan". Current Biology. 30 (21): 4238–4244.e1. doi:10.1016/j.cub.2020.07.078.
  34. Yang, Xianfeng; Kimmig, Julien; Cameron, Christopher B.; Nanglu, Karma; Kimmig, Sara R.; Carle, Danielle de; Zhang, Caixia; Yu, Mengxiao; Peng, Hanchi (2 March 2024). "An early Cambrian pelago-benthic acorn worm and the origin of the hemichordate larva". Palaeontologia Electronica. 27 (1). Paleontological Society: 1–19. doi:10.26879/1356. ISSN 1094-8074.
  35. Maletz, Jörg (October 2026). "Graptolite diversity — How much do we know?". Palaeoworld. 35 (5): 201150. doi:10.1016/j.palwor.2026.201150.{{cite journal}}: CS1 maint: article number as page number (link)
  36. Shao, T.Q.; Wang, Q.; Liu, Y.H.; Qin, J.C.; Zhang, Y.N.; Liu, M.J.; Shao, Y.; Zhao, J.Y.; Zhang, H.Q. (October 2020). "A new scalidophoran animal from the Cambrian Fortunian Stage of South China and its implications for the origin and early evolution of Kinorhyncha". Precambrian Research. 349: 105616. doi:10.1016/j.precamres.2020.105616.{{cite journal}}: CS1 maint: article number as page number (link)
  37. Harvey, Thomas H. P.; Butterfield, Nicholas J. (30 January 2017). "Exceptionally preserved Cambrian loriciferans and the early animal invasion of the meiobenthos". Nature Ecology & Evolution. 1 (3). Nature Publishing Group: 0022. doi:10.1038/s41559-016-0022. ISSN 2397-334X.
  38. Møbjerg Kristensen, Reinhardt; Funch, Peter (2000). "Micrognathozoa: A new class with complicated jaws like those of Rotifera and Gnathostomulida". Journal of Morphology (in French). 246 (1): 1–49. doi:10.1002/1097-4687(200010)246:1<1::AID-JMOR1>3.0.CO;2-D. ISSN 1097-4687.
  39. 1 2 3 4 5 6 7 8 9 Brusca, Richard C.; Brusca, Gary J. (2017). Invertebrates. Oxford University Press, Incorporated, Sinauer Associates, Inc. ISBN 978-1-60535-375-3. OCLC 928750550.
  40. Feldkamp, S. (2002) Modern Biology. Holt, Rinehart, and Winston, USA. (pp. 725)
  41. Bleidorn, Christoph; Schmidt‐Rhaesa, Andreas; Garey, James R. (November 2002). "Systematic relationships of Nematomorpha based on molecular and morphological data". Invertebrate Biology. 121 (4): 357–364. doi:10.1111/j.1744-7410.2002.tb00136.x. ISSN 1077-8306.
  42. Marotta, R.; Ruhberg, H. (November 2004). "Sperm ultrastructure of an oviparous and an ovoviviparous onychophoran species (Peripatopsidae) with some phylogenetic considerations". Journal of Zoological Systematics and Evolutionary Research. 42 (4): 313–322. doi:10.1111/j.1439-0469.2004.00278.x. ISSN 0947-5745.
  43. 1 2 3 4 5 6 Schmidt-Rhaesa, Andreas (2018). Miscellaneous Invertebrates. de Gruyter GmbH, Walter. ISBN 978-3-11-048927-9.
  44. 1 2 Neresheimer, Eugen (October 1933). Grimpe, Georg; Wagler, Erich (eds.). "II. Mesozoa" (PDF). Tierwelt der Nord- und Ostsee (in German): 8 via VLIZ.
  45. Kozloff, E. N. (1992). "The genera of the phylum Orthonectida". Cahiers de biologie marine. 33 (3): 377–406 via VLIZ.
  46. Caullery, MJGC; Mesnil, Félix (1904). Comptes rendus hebdomadaires des séances et mémoires de la Société de biologie [Weekly Reports of the Meetings and Memoirs of the Society of Biology.] (in French). Paris: Société de biologie.
  47. Knaust, Dirk (7 October 2021). "A microbialite with its entombed benthic community from the Middle Triassic (Anisian-Ladinian) Muschelkalk Group of Germany". Palaeontographica Abteilung A. 320 (1–3): 1–63. doi:10.1127/pala/2021/0114. ISSN 0375-0442.
  48. Naimark, Elena; Lyupina, Yulia; Finoshin, Alexander; Nikitin, Mikhail (18 November 2025). "TAPHONOMIC EXPERIMENTS SHED LIGHT ON FOSSILIZATION POTENTIAL OF PLACOZOA". PALAIOS. 40 (11): 336–348. doi:10.2110/palo.2024.020. ISSN 0883-1351.
  49. Smith, Julian P. S.; Teyler, Seth; Rieger, Reinhard M. (1 January 1986). "Is the Turbellaria polyphyletic?". Hydrobiologia. 132 (1): 13–21. doi:10.1007/BF00046223. ISSN 1573-5117.
  50. Hestetun, Jon Thomassen; Vacelet, Jean; Boury-Esnault, Nicole; Borchiellini, Carole; Kelly, Michelle; Ríos, Pilar; Cristobo, Javier; Rapp, Hans Tore (January 2016). "The systematics of carnivorous sponges". Molecular Phylogenetics and Evolution. 94: 327–345. doi:10.1016/j.ympev.2015.08.022.
  51. Leys, S.P.; Mackie, G.O.; Reiswig, H.M. (2007), "The Biology of Glass Sponges", Advances in Marine Biology, vol. 52, Elsevier, pp. 1–145, doi:10.1016/S0065-2881(06)52001-2, ISBN 978-0-12-373718-2, retrieved 3 September 2026{{citation}}: CS1 maint: work parameter with ISBN (link)
  52. 1 2 Ereskovsky, Alexander; Melnikov, Nikolai P.; Lavrov, Andrey (April 2025). "Archaeocytes in sponges: simple cells of complicated fate". Biological Reviews. 100 (2): 790–814. doi:10.1111/brv.13162. ISSN 1464-7931.
  53. Ereskovsky, Alexander V.; Borisenko, Ilya E.; Lapébie, Pascal; Gazave, Eve; Tokina, Daria B.; Borchiellini, Carole (13 August 2015). Singh, Shree Ram (ed.). "Oscarella lobularis (Homoscleromorpha, Porifera) Regeneration: Epithelial Morphogenesis and Metaplasia". PLOS ONE. 10 (8): e0134566. doi:10.1371/journal.pone.0134566. ISSN 1932-6203. PMC 4536211. PMID 26270639.{{cite journal}}: CS1 maint: article number as page number (link)
  54. Ereskovsky, Alexander; Lavrov, Andrey (23 March 2021), LaDouceur, Elise E.B. (ed.), "Porifera", Invertebrate Histology (1 ed.), Wiley, pp. 19–54, doi:10.1002/9781119507697.ch2, ISBN 978-1-119-50765-9, retrieved 17 September 2026{{citation}}: CS1 maint: work parameter with ISBN (link)
  55. Gazave, Eve; Lapébie, Pascal; Renard, Emmanuelle; Vacelet, Jean; Rocher, Caroline; Ereskovsky, Alexander V.; Lavrov, Dennis V.; Borchiellini, Carole (14 December 2010). "Molecular Phylogeny Restores the Supra-Generic Subdivision of Homoscleromorph Sponges (Porifera, Homoscleromorpha)". PLOS ONE. 5 (12). Public Library of Science: e14290. doi:10.1371/journal.pone.0014290. ISSN 1932-6203. PMC 3001884. PMID 21179486.{{cite journal}}: CS1 maint: article number as page number (link)
  56. 1 2 Senatore, Adriano; Raiss, Hamad; Le, Phuong (4 November 2016). "Physiology and Evolution of Voltage-Gated Calcium Channels in Early Diverging Animal Phyla: Cnidaria, Placozoa, Porifera and Ctenophora". Frontiers in Physiology. 7. Frontiers. doi:10.3389/fphys.2016.00481. ISSN 1664-042X. PMC 5095125. PMID 27867359.
  57. Hartigan, A.; Estensoro, I.; Vancová, M.; Bílý, T.; Patra, S.; Eszterbauer, E.; Holzer, A. S. (16 December 2016). "New cell motility model observed in parasitic cnidarian Sphaerospora molnari (Myxozoa:Myxosporea) blood stages in fish". Scientific Reports. 6 (1). doi:10.1038/srep39093. ISSN 2045-2322. PMC 5159882. PMID 27982057.
  58. Patra, Sneha; Hartigan, Ashlie; Morris, David J.; KodáDková, Alena; Holzer, Astrid S. (April 2017). "Description and experimental transmission of Tetracapsuloides vermiformis n. sp. (Cnidaria: Myxozoa) and guidelines for describing malacosporean species including reinstatement of Buddenbrockia bryozoides n. comb. (syn. Tetracapsula bryozoides )". Parasitology. 144 (4): 497–511. doi:10.1017/S0031182016001931. ISSN 0031-1820.
  59. Zverkov, Oleg A.; Mikhailov, Kirill V.; Isaev, Sergey V.; Rusin, Leonid Y.; Popova, Olga V.; Logacheva, Maria D.; Penin, Alexey A.; Moroz, Leonid L.; Panchin, Yuri V.; Lyubetsky, Vassily A.; Aleoshin, Vladimir V. (24 May 2019). "Dicyemida and Orthonectida: Two Stories of Body Plan Simplification". Frontiers in Genetics. 10. Frontiers. doi:10.3389/fgene.2019.00443. ISSN 1664-8021. PMC 6543705. PMID 31178892.
  60. Kusztyb, Samara; Januszkiewicz, Warren; Walsh, Elizabeth J.; Hochberg, Rick; Wallace, Robert L. (July 2024). "Does "form follow function" in the rotiferan genus Keratella?". Hydrobiologia. 851 (12–13): 3079–3096. doi:10.1007/s10750-023-05192-9. ISSN 0018-8158.
  61. Garey, James R.; Schmidt-Rhaesa, Andreas; Near, Thomas J.; Nadler, Steven A. (January 1998). "The evolutionary relationships of rotifers and acanthocephalans". Hydrobiologia. 387–388 (0): 83–91. doi:10.1023/A:1017060902909. ISSN 0018-8158.
  62. Luo, Cihang; Parry, Luke A.; Boudinot, Brendon E.; Wang, Shengyu; Jarzembowski, Edmund A.; Zhang, Haichun; Wang, Bo (May 2025). "A Jurassic acanthocephalan illuminates the origin of thorny-headed worms". Nature. 641 (8063). Nature Publishing Group: 674–680. doi:10.1038/s41586-025-08830-5. ISSN 1476-4687.
  63. "rotifers and dwarf males and rotifers". www.plingfactory.de. Retrieved 23 September 2026.
  64. Funch, Peter; Sørensen, Martin Vinther; Obst, Matthias (September 2005). "On the Phylogenetic Position of Rotifera – Have We Come Any Further?". Hydrobiologia. 546 (1): 11–28. doi:10.1007/s10750-005-4093-6. ISSN 0018-8158.
  65. Wang, Deng; Qiang, Yaqin; Guo, Junfeng; Vannier, Jean; Song, Zuchen; Peng, Jiaxin; Zhang, Boyao; Sun, Jie; Yu, Yilun (19 February 2024), Early evolution of the ecdysozoan body plan, doi:10.7554/eLife.94709.1, retrieved 27 August 2026{{citation}}: CS1 maint: unflagged free DOI (link)
  66. Wang, Deng; Qiang, Yaqin; Guo, Junfeng; Vannier, Jean; Song, Zuchen; Peng, Jiaxin; Zhang, Boyao; Sun, Jie; Yu, Yilun (8 July 2024). "Early evolution of the ecdysozoan body plan". eLife. eLife Sciences Publications Limited. doi:10.7554/eLife.94709. Retrieved 28 August 2026.{{cite web}}: CS1 maint: unflagged free DOI (link)
  67. Liu, Yunhuan; Zhang, Huaqiao; Xiao, Shuhai; Shao, Tiequan; Duan, Baichuan (6 September 2020), An early Cambrian ecdysozoan with a terminal mouth but no anus, doi:10.1101/2020.09.04.283960, retrieved 28 August 2026
  68. Persson, Dennis K.; Halberg, Kenneth A.; Jørgensen, Aslak; Møbjerg, Nadja; Kristensen, Reinhardt M. (2012). "Neuroanatomy of Halobiotus crispae (Eutardigrada: Hypsibiidae): Tardigrade brain structure supports the clade panarthropoda". Journal of Morphology. 273 (11): 1227–1245. doi:10.1002/jmor.20054. ISSN 1097-4687.
  69. Mapalo, Marc A.; Wolfe, Joanna M.; Ortega-Hernández, Javier (6 August 2024). "Cretaceous amber inclusions illuminate the evolutionary origin of tardigrades". Communications Biology. 7 (1). Nature Publishing Group: 953. doi:10.1038/s42003-024-06643-2. ISSN 2399-3642. PMC 11303527. PMID 39107512.
  70. 1 2 Cavalier-Smith, Thomas (22 June 2004). "Only Six Kingdoms of Life". Proceedings: Biological Sciences. 271 (1545): 1251–1262. doi:10.1098/rspb.2004.2705. PMC 1691724. PMID 15306349.
  71. Mauseth 2012, pp. 514, 517.
  72. 1 2 Cronquist, A.; A. Takhtajan; W. Zimmermann (April 1966). "On the higher taxa of Embryobionta". Taxon. 15 (4): 129–134. Bibcode:1966Taxon..15..129C. doi:10.2307/1217531. JSTOR 1217531.
  73. Chase, Mark W. & Reveal, James L. (October 2009), "A phylogenetic classification of the land plants to accompany APG III", Botanical Journal of the Linnean Society, 161 (2): 122–127, doi:10.1111/j.1095-8339.2009.01002.x
  74. 1 2 3 Mauseth, James D. (2012). Botany: An Introduction to Plant Biology (5th ed.). Sudbury, MA: Jones and Bartlett Learning. ISBN 978-1-4496-6580-7. p. 489
  75. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 Margulis, Lynn; Chapman, Michael J. (2009). Kingdoms and Domains: An Illustrated Guide to the Phyla of Life on Earth (4th corrected ed.). London: Academic Press. ISBN 978-0-12-373621-5.
  76. Mauseth 2012, p. 540.
  77. Mauseth 2012, p. 542.
  78. Mauseth 2012, p. 543.
  79. Mauseth 2012, p. 509.
  80. Crandall-Stotler, Barbara; Stotler, Raymond E. (2000). "Morphology and classification of the Marchantiophyta". In A. Jonathan Shaw; Bernard Goffinet (eds.). Bryophyte Biology. Cambridge: Cambridge University Press. p. 21. ISBN 978-0-521-66097-6.
  81. Mauseth 2012, p. 535.
  82. Wyatt, T.; Wösten, H.; Dijksterhuis, J. (2013). "Advances in Applied Microbiology Chapter 2 - Fungal Spores for Dispersion in Space and Time". Advances in Applied Microbiology. 85: 43–91. doi:10.1016/B978-0-12-407672-3.00002-2. PMID 23942148.
  83. Holt, Jack R.; Iudica, Carlos A. (1 October 2016). "Blastocladiomycota". Diversity of Life. Susquehanna University. Retrieved 29 December 2016.
  84. Holt, Jack R.; Iudica, Carlos A. (9 January 2014). "Chytridiomycota". Diversity of Life. Susquehanna University. Retrieved 29 December 2016.
  85. "Chytridiomycota | phylum of fungi". Encyclopedia Britannica. Retrieved 5 May 2019.
  86. McConnaughey, M (2014). "Physical Chemical Properties of Fungi☆". Physical Chemical Properties of Fungi. doi:10.1016/B978-0-12-801238-3.05231-4. ISBN 978-0-12-801238-3.
  87. Taylor, Thomas; Krings, Michael; Taylor, Edith (2015). "Fossil Fungi Chapter 4 - Chytridiomycota". Fossil Fungi: 41–67. doi:10.1016/b978-0-12-387731-4.00004-9.
  88. Holt, Jack R.; Iudica, Carlos A. (12 March 2013). "Microsporidia". Diversity of Life. Susquehanna University. Retrieved 29 December 2016.
  89. Holt, Jack R.; Iudica, Carlos A. (23 April 2013). "Neocallimastigomycota". Diversity of Life. Susquehanna University. Retrieved 29 December 2016.
  90. 1 2 "Types of Fungi". BiologyWise. 22 May 2009. Archived from the original on 5 May 2019. Retrieved 5 May 2019.
  91. Wang, Xuewei; Liu, Xingzhong; Groenewald, Johannes Z. (2017). "Phylogeny of anaerobic fungi (phylum Neocallimastigomycota), with contributions from yak in China". Antonie van Leeuwenhoek. 110 (1): 87–103. doi:10.1007/s10482-016-0779-1. PMC 5222902. PMID 27734254.
  92. 1 2 Hibbett DS, Binder M, Bischoff JF, Blackwell M, Cannon PF, Eriksson OE, et al. (May 2007). "A higher-level phylogenetic classification of the Fungi" (PDF). Mycological Research. 111 (Pt 5): 509–47. doi:10.1016/j.mycres.2007.03.004. PMID 17572334. S2CID 4686378. Archived from the original (PDF) on 26 March 2009.
  93. 1 2 Ruggiero, Michael A.; Gordon, Dennis P.; Orrell, Thomas M.; et al. (29 April 2015). "A Higher Level Classification of All Living Organisms". PLOS ONE. 10 (6) e0119248. Bibcode:2015PLoSO..1019248R. doi:10.1371/journal.pone.0119248. PMC 4418965. PMID 25923521.
  94. White, Merlin M.; James, Timothy Y.; O'Donnell, Kerry; et al. (November–December 2006). "Phylogeny of the Zygomycota Based on Nuclear Ribosomal Sequence Data". Mycologia. 98 (6): 872–884. doi:10.1080/15572536.2006.11832617. PMID 17486964. S2CID 218589354.
  95. Hagen, Joel B. (January 2012). "Five Kingdoms, More or Less: Robert Whittaker and the Broad Classification of Organisms". BioScience. 62 (1): 67–74. Bibcode:2012BiSci..62...67H. doi:10.1525/bio.2012.62.1.11.
  96. Blackwell, Will H.; Powell, Martha J. (June 1999). "Reconciling Kingdoms with Codes of Nomenclature: Is It Necessary?". Systematic Biology. 48 (2): 406–412. doi:10.1080/106351599260382. PMID 12066717.
  97. Davis, R. A. (19 March 2012). "Kingdom PROTISTA". College of Mount St. Joseph. Archived from the original on 4 August 2022. Retrieved 28 December 2016.
  98. 1 2 "Taxonomic tree". Catalogue of Life. 23 December 2016. Archived from the original on 1 August 2021. Retrieved 28 December 2016.
  99. 1 2 Cavalier-Smith T (2022). "Ciliary transition zone evolution and the root of the eukaryote tree: implications for opisthokont origin and classification of kingdoms Protozoa, Plantae, and Fungi". Protoplasma. 259 (3): 487–593. Bibcode:2022Prpls.259..487C. doi:10.1007/s00709-021-01665-7. PMC 9010356. PMID 34940909.
  100. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Adl SM, Bass D, Lane CE, Lukeš J, Schoch CL, Smirnov A, Agatha S, Berney C, Brown MW, Burki F, Cárdenas P, Čepička I, Chistyakova L, del Campo J, Dunthorn M, Edvardsen B, Eglit Y, Guillou L, Hampl V, Heiss AA, Hoppenrath M, James TY, Karnkowska A, Karpov S, Kim E, Kolisko M, Kudryavtsev A, Lahr DJ, Lara E, Le Gall L, Lynn DH, Mann DG, Massana R, Mitchell EA, Morrow C, Park JS, Pawlowski JW, Powell MJ, Richter DJ, Rueckert S, Shadwick L, Shimano S, Spiegel FW, Torruella G, Youssef N, Zlatogursky V, Zhang Q (2019). "Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes". Journal of Eukaryotic Microbiology. 66 (1): 4–119. doi:10.1111/jeu.12691. PMC 6492006. PMID 30257078.
  101. 1 2 Pawlowski J, Audic S, Adl S, Bass D, Belbahri L, Berney C, et al. (6 November 2012). "CBOL protist working group: barcoding eukaryotic richness beyond the animal, plant, and fungal kingdoms". PLOS Biology. 10 (11) e1001419. doi:10.1371/journal.pbio.1001419. PMC 3491025. PMID 23139639.
  102. 1 2 Votýpka J, Modrý D, Oborník M, Šlapeta J, Lukeš J (2016). "Apicomplexa". In Archibald J, Simpson AG, Slamovits CH, Margulis L, Melkonian M, Chapman DJ, Corliss JO (eds.). Handbook of the Protists. Cham: Springer. pp. 1–58. doi:10.1007/978-3-319-32669-6_20-1. ISBN 978-3-319-32669-6.
  103. Jan Janouškovec; Denis Tikhonenkov; Fabien Burki; Alexis T Howe; Martin Kolísko; Alexander P Mylnikov; Patrick John Keeling (2015). "Factors mediating plastid dependency and the origins of parasitism in apicomplexans and their close relatives". Proceedings of the National Academy of Sciences of the United States of America. 112 (33): 10200–10207. Bibcode:2015PNAS..11210200J. doi:10.1073/pnas.1423790112. PMC 4547307. PMID 25717057. Wikidata Q30662251.
  104. 1 2 3 4 5 6 Michael D. Guiry (2024). "How many species of algae are there? A reprise. Four kingdoms, 14 phyla, 63 classes and still growing". Journal of Phycology. 00: 1–15. doi:10.1111/jpy.13431. PMID 38245909. Wikidata Q124684077.
  105. Foissner, W.; Hawksworth, David, eds. (2009). Protist Diversity and Geographical Distribution. Topics in Biodiversity and Conservation. Vol. 8. Springer Netherlands. p. 111. doi:10.1007/978-90-481-2801-3. ISBN 978-90-481-2800-6.
  106. 1 2 3 T Cavalier-Smith (2002). "The phagotrophic origin of eukaryotes and phylogenetic classification of Protozoa". International Journal of Systematic and Evolutionary Microbiology. 52 (2): 297–354. doi:10.1099/00207713-52-2-297. PMID 11931142. Wikidata Q28212529.
  107. 1 2 3 4 Cavalier-Smith T (2013). "Early evolution of eukaryote feeding modes, cell structural diversity, and classification of the protozoan phyla Loukozoa, Sulcozoa, and Choanozoa". European Journal of Protistology. 49 (2): 115–178. doi:10.1016/j.ejop.2012.06.001. PMID 23085100.
  108. 1 2 W Foissner; H Blatterer; I Foissner (1988). "The hemimastigophora (Hemimastix amphikineta nov. gen., nov. spec.), a new protistan phylum from gondwanian soils". European Journal of Protistology. 23 (4): 361–383. doi:10.1016/s0932-4739(88)80027-0. PMID 23195325. Wikidata Q85570914.
  109. Gordon Lax; Yana Eglit; Laura Eme; Erin M Bertrand; Andrew J Roger; Alastair G B Simpson (2018). "Hemimastigophora is a novel supra-kingdom-level lineage of eukaryotes". Nature. 564 (7736): 410–414. doi:10.1038/s41586-018-0708-8. PMID 30429611. Wikidata Q58834974.
  110. Shɨshkin, Yegor (2022). "Spironematella terricola comb. n. and Spironematella goodeyi comb. n. (Hemimastigida = Hemimastigea = Hemimastigophora) for Spironema terricola and Spironema goodeyi with diagnoses of the genus and family Spironematellidae amended". Zootaxa. 5128 (2): 295–297. doi:10.11646/zootaxa.5128.2.8. PMID 36101172. S2CID 252220401.
  111. 1 2 3 Pánek, Tomáš; Tice, Alexander K.; Corre, Pia; Hrubá, Pavla; Žihala, David; Kamikawa, Ryoma; Yazaki, Euki; Shiratori, Takashi; Kume, Keitaro; Hashimoto, Tetsuo; Ishida, Ken-ichiro; Hradilová, Miluše; Silberman, Jeffrey D.; Roger, Andrew; Inagaki, Yuji; Eliáš, Marek; Brown, Matthew W.; Čepička, Ivan (16 January 2025). "An expanded phylogenomic analysis of Heterolobosea reveals the deep relationships, non-canonical genetic codes, and cryptic flagellate stages in the group". Molecular Phylogenetics and Evolution. 204 108289. Bibcode:2025MolPE.20408289P. doi:10.1016/j.ympev.2025.108289. PMID 39826589.
  112. Heiss AA, Warring SD, Lukacs K, Favate J, Yang A, Gyaltshen Y, Filardi C, Simpson AG, Kim E (December 2020). "Description of Imasa heleensis, gen. nov., sp. nov. (Imasidae, fam. nov.), a Deep-Branching Marine Malawimonad and Possible Key Taxon in Understanding Early Eukaryotic Evolution". Journal of Eukaryotic Microbiology. 68 (2) e12837. doi:10.1111/jeu.12837. PMID 33274482.
  113. Karpov, Sergey; Mamkaeva, Maria A.; Aleoshin, Vladimir; Nassonova, Elena; Lilje, Osu; Gleason, Frank H. (1 January 2014). "Morphology, phylogeny, and ecology of the aphelids (Aphelidea, Opisthokonta) and proposal for the new superphylum Opisthosporidia". Frontiers in Microbiology. 5: 112. Bibcode:2014FrMic...500112K. doi:10.3389/fmicb.2014.00112. PMC 3975115. PMID 24734027.
  114. 1 2 3 Denis V. Tikhonenkov, Kirill V. Mikhailov, Ryan M. R. Gawryluk, Artem O. Belyaev, Varsha Mathur, Sergey A. Karpov, Dmitry G. Zagumyonnyi, Anastasia S. Borodina, Kristina I. Prokina, Alexander P. Mylnikov, Vladimir V. Aleoshin & Patrick J. Keeling (2022). "Microbial predators form a new supergroup of eukaryotes". Nature. 612: 714–719. doi:10.1038/s41586-022-05511-5. PMID 36477531. Wikidata Q115933632.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  115. Thomas Cavalier-Smith; Ema E-Y Chao (2006). "Phylogeny and megasystematics of phagotrophic heterokonts (kingdom Chromista)". Journal of Molecular Evolution. 62 (4): 388–420. doi:10.1007/s00239-004-0353-8. PMID 16557340. Wikidata Q28303534.
  116. Thines M (2018). "Oomycetes". Current Biology. 28 (15): R812–R813. doi:10.1016/j.cub.2018.05.062. PMID 30086308.
  117. T Cavalier-Smith (1999). "Principles of protein and lipid targeting in secondary symbiogenesis: euglenoid, dinoflagellate, and sporozoan plastid origins and the eukaryote family tree". Journal of Eukaryotic Microbiology. 46 (4): 347–66. doi:10.1111/j.1550-7408.1999.tb04614.x. PMID 18092388. Wikidata Q28261633.
  118. 1 2 Shalchian-Tabrizi, K; Eikrem, W; Klaveness, D; Vaulot, D; Minge, M.A; Le Gall, F; Romari, K; Throndsen, J; Botnen, A; Massana, R; Thomsen, H.A; Jakobsen, K.S (28 April 2006). "Telonemia, a new protist phylum with affinity to chromist lineages". Proceedings of the Royal Society B: Biological Sciences. 273 (1595): 1833–1842. Bibcode:2006PBioS.273.1833S. doi:10.1098/rspb.2006.3515. PMC 1634789. PMID 16790418.
  119. 1 2 Tikhonenkov, Denis V.; Jamy, Mahwash; Borodina, Anastasia S.; Belyaev, Artem O.; Zagumyonnyi, Dmitry G.; Prokina, Kristina I.; Mylnikov, Alexander P.; Burki, Fabien; Karpov, Sergey A. (2022). "On the origin of TSAR: morphology, diversity and phylogeny of Telonemia". Open Biology. 12 (3) 210325. The Royal Society. doi:10.1098/rsob.210325. ISSN 2046-2441. PMC 8924772. PMID 35291881.
  120. Corliss, John O. (1984). "The Kingdom Protista and its 45 Phyla". BioSystems. 17 (2): 87–176. Bibcode:1984BiSys..17...87C. doi:10.1016/0303-2647(84)90003-0. PMID 6395918.
  121. 1 2 Euzéby JP, Parte AC. "Names of phyla". List of Prokaryotic names with Standing in Nomenclature (LPSN). Retrieved 3 April 2022.
  122. 1 2 3 Göker, Markus; Oren, Aharon (2023). "Valid publication of four additional phylum names". International Journal of Systematic and Evolutionary Microbiology. 73 (9). Microbiology Society: 006024. doi:10.1099/ijsem.0.006024. ISSN 1466-5034. PMID 37695645.
  123. Göker, Markus; Oren, Aharon (2024). "Valid publication of names of two domains and seven kingdoms of prokaryotes". International Journal of Systematic and Evolutionary Microbiology. 74 (1). Microbiology Society: 006242. doi:10.1099/ijsem.0.006242. ISSN 1466-5034. PMID 38252124.
  124. Imachi, Hiroyuki; Nobu, Masaru K.; Kato, Shingo; Takaki, Yoshihiro; Miyazaki, Masayuki; Miyata, Makoto; Ogawara, Miyuki; Saito, Yumi; Sakai, Sanae; Tahara, Yuhei O.; Takano, Yoshinori; Tasumi, Eiji; Uematsu, Katsuyuki; Yoshimura, Toshihiro; Itoh, Takashi (2024). "Promethearchaeum syntrophicum gen. nov., sp. nov., an anaerobic, obligately syntrophic archaeon, the first isolate of the lineage 'Asgard' archaea, and proposal of the new archaeal phylum Promethearchaeota phyl. nov. and kingdom Promethearchaeati regn. nov". International Journal of Systematic and Evolutionary Microbiology. 74 (7). Microbiology Society: 006435. doi:10.1099/ijsem.0.006435. ISSN 1466-5034. PMC 11316595. PMID 38967634.
  125. Oren, Aharon; Garrity, George M. (2021). "Valid publication of the names of forty-two phyla of prokaryotes". International Journal of Systematic and Evolutionary Microbiology. 71 (10). Microbiology Society: 005056. doi:10.1099/ijsem.0.005056. ISSN 1466-5034. PMID 34694987.
  126. "Phylum". lpsn.dsmz.de. Retrieved 27 August 2026.
[edit]