Agnatha (/ˈæɡnəθə, æɡˈneɪθə/;^[3] from Ancient Greek ἀ- (a-) 'without', and γνάθος (gnáthos) 'jaws') is an infraphylum^[4] of jawless fish in the phylum Chordata, subphylum Vertebrata, consisting of both living (cyclostomes) and extinct (conodonts, anaspids, and ostracoderms) species. Among recent animals, cyclostomes are sister to all vertebrates with jaws, known as gnathostomes.^[5]

Quick Facts Scientific classification, Groups included ...

Agnatha Temporal range: Cambrian Stage 3–Present, [1] PreꞒ Ꞓ O S D C P T J K Pg N
Lampetra fluviatilis
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Chordata
Subphylum:	Vertebrata
Infraphylum:	Agnatha Cope, 1889
Groups included
†Myllokunmingiida †Metaspriggina? †Haikouellidae †Conodonta Ostracodermi †Pteraspidomorphi †Thelodontomorphi †Thelodonti [2] †Anaspidomorphi †Cephalaspidomorphi Cyclostomi †Palaeospondylus?
Cladistically included but traditionally excluded taxa
Gnathostomata (from Cephalaspidomorphi)

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Molecular data, both from rRNA^[6] and from mtDNA^[7] as well as embryological data,^[8] strongly supports the hypothesis that both groups of living agnathans, hagfishes and lampreys, are more closely related to each other than to jawed fish, forming the clade Cyclostomi.^[9]

The oldest fossil agnathans appeared in the Cambrian, and two groups still survive today: the lampreys and the hagfish, comprising about 120 species in total. Hagfish are considered members of the subphylum Vertebrata, because they secondarily lost vertebrae; before this event was inferred from molecular^[6][7][10] and developmental^[11] data, the group Craniata was created by Linnaeus (and is still sometimes used as a strictly morphological descriptor) to reference hagfish plus vertebrates.

While a few scientists still regard the living agnathans as only superficially similar, and argue that many of these similarities are probably shared basal characteristics of ancient vertebrates, newer taxonomic studies clearly place hagfish (the Myxini or Hyperotreti) with the lampreys (Hyperoartii) as being more closely related to each other than either is to the jawed fishes.^[6][7][12]

Agnathans are ectothermic, meaning they do not regulate their own body temperature. Agnathan metabolism is slow in cold water, and therefore they do not have to eat very much. They have no distinct stomach, but rather a long gut, more or less homogeneous throughout its length. Lampreys feed on other fish and mammals. Anticoagulant fluids preventing blood clotting are injected into the host, causing the host to yield more blood. Hagfish are scavengers, eating mostly dead animals. They use a row of sharp teeth to break down the animal. The fact that Agnathan teeth are unable to move up and down limits their possible food types.

In addition to the absence of jaws, modern agnathans are characterised by absence of paired fins; the presence of a notochord both in larvae and adults; and seven or more paired gill pouches. Lampreys have a light sensitive pineal eye (homologous to the pineal gland in mammals). All living and most extinct Agnatha do not have an identifiable stomach or any appendages. Fertilization and development are both external. There is no parental care in the Agnatha class. The Agnatha are ectothermic or cold , with a cartilaginous skeleton, and the heart contains 2 chambers.

Fertilization in lampreys is external. Mode of fertilization in hagfishes is not known. Development in both groups probably is external. There is no known parental care. Not much is known about the hagfish reproductive process. It is believed that hagfish only have 30 eggs over a lifetime.^[14] There is very little of the larval stage that characterizes the lamprey. Lamprey are only able to reproduce once. After external fertilization, the lamprey's cloacas remain open, allowing a fungus to enter their intestines, killing them. Lampreys reproduce in freshwater riverbeds, working in pairs to build a nest and burying their eggs about an inch beneath the sediment. The resulting hatchlings go through four years of larval development before becoming adults.

Although a minor element of modern marine fauna, agnathans were prominent among the early fish in the early Paleozoic. Two types of Early Cambrian animal apparently having fins, vertebrate musculature, and gills are known from the early Cambrian Maotianshan shales of China: Haikouichthys and Myllokunmingia. They have been tentatively assigned to Agnatha by Janvier. A third possible agnathid from the same region is Haikouella. A possible agnathid that has not been formally described was reported by Simonetti from the Middle Cambrian Burgess Shale of British Columbia. Conodonts, a class of agnathans which arose in the early Cambrian,^[16] remained common enough until their extinction in the Triassic that their teeth (the only parts of them that were usually fossilized) are often used as index fossils from the late Cambrian to the Triassic.^[17]

Many Ordovician, Silurian, and Devonian agnathans were armored with heavy bony-spiky plates. The first armored agnathans—the Ostracoderms, precursors to the bony fish and hence to the tetrapods (including humans)—are known from the middle Ordovician, and by the Late Silurian the agnathans had reached the high point of their evolution. Most of the ostracoderms, such as thelodonts, osteostracans, and galeaspids, were more closely related to the gnathostomes than to the surviving agnathans, known as cyclostomes. Cyclostomes apparently split from other agnathans before the evolution of dentine and bone, which are present in many fossil agnathans, including conodonts.^[18] Agnathans declined in the Devonian and never recovered.

Approximately 500 million years ago, two types of recombinatorial adaptive immune systems (AISs) arose in vertebrates. The jawed vertebrates diversify their repertoire of immunoglobulin domain-based T and B cell antigen receptors mainly through the rearrangement of V(D)J gene segments and somatic hypermutation, but none of the fundamental AIS recognition elements in jawed vertebrates have been found in jawless vertebrates. Instead, the AIS of jawless vertebrates is based on variable lymphocyte receptors (VLRs) that are generated through recombinatorial usage of a large panel of highly diverse leucine-rich-repeat (LRR) sequences.^[19] Three VLR genes (VLRA, VLRB, and VLRC) have been identified in lampreys and hagfish, and are expressed on three distinct lymphocytes lineages. VLRA+ cells and VLRC+ cells are T-cell-like and develop in a thymus-like lympho-epithelial structure, termed thymoids. VLRB+ cells are B-cell-like, develop in hematopoietic organs, and differentiate into "VLRB antibody"-secreting plasma cells.^[20]

Phylogeny based on the work of Mikko Haaramo and Delsuc et al.^[40][41]

While the "agnatha" Conodonta was indeed jawless, if it would have continued to live, its descendants would still be closer related to e.g. humans than to lampreys, and also contempory it was closer related to the ancestor of humans. Due to such considerations, Agnatha can not be consolidated into a coherent grouping without either removing any non-cyclostomata, or by including all vertebrata thus rendering it into a junior synonym of vertebrata.

The new phylogeny from Miyashita et al. (2019) is considered compatible with both morphological and molecular evidence.^[42]

• Gnathostomata
• Amphirhina, an alternate name for the above parallel, or sister, classification
• Cyclostomata